DATE ADDED TO CATALOG PUBMEDID FIRST AUTHOR DATE JOURNAL LINK STUDY DISEASE/TRAIT INITIAL SAMPLE SIZE REPLICATION SAMPLE SIZE PLATFORM [SNPS PASSING QC] ASSOCIATION COUNT MAPPED_TRAIT MAPPED_TRAIT_URI STUDY ACCESSION GENOTYPING TECHNOLOGY 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Insomnia complaints 12,863 European ancestry male cases, 19,521 European ancestry female cases, 40,776 European ancestry male controls, 39,846 European ancestry female controls 1,983 Icelandic ancestry male cases, 1,791 Icelandic ancestry female cases, 2,064 Icelandic ancestry male controls, 1,727 Icelandic ancestry female controls Affymetrix [at least 12428592] (imputed) 2 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST004695 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Sleep duration 112,411 European ancestry male individuals NA Affymetrix [at least 12428592] (imputed) 3 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST004694 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Insomnia complaints (sex interaction) 12,863 European ancestry male cases, 19,521 European ancestry female cases, 40,776 European ancestry male controls, 39,846 European ancestry female controls NA Affymetrix [at least 12428592] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST004700 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Insomnia complaints (continuous) 12,863 European ancestry male cases, 19,521 European ancestry female cases, 40,776 European ancestry male controls, 39,846 European ancestry female controls NA Affymetrix [at least 12428592] (imputed) 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST004701 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Insomnia complaints (dichotomous) 32,384 European ancestry cases, 27,128 European ancestry controls NA Affymetrix [at least 12428592] (imputed) 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST004702 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Chronotype 101,185 European ancestry individuals NA Affymetrix [at least 12428592] (imputed) 9 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST004696 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Ease of getting up in the morning 112,866 European ancestry individuals NA Affymetrix [at least 12428592] (imputed) 5 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST004697 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Daytime nap 113,054 European ancestry cases and controls NA Affymetrix [at least 12428592] (imputed) 4 daytime rest measurement http://www.ebi.ac.uk/efo/EFO_0007828 GCST004693 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Snoring 105,377 European ancestry cases and controls NA Affymetrix [at least 12428592] (imputed) 1 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST004698 Genome-wide genotyping array 2017-09-11 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Daytime sleepiness 112,717 European ancestry cases and controls NA Affymetrix [at least 12428592] (imputed) 6 excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0007875 GCST004699 Genome-wide genotyping array 2018-11-02 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Insomnia complaints 19,521 European ancestry female cases, 39,846 European ancestry female controls 1,983 Icelandic ancestry male cases, 1,791 Icelandic ancestry female cases, 2,064 Icelandic ancestry male controls, 1,727 Icelandic ancestry female controls Affymetrix [at least 12428592] (imputed) 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST006487 Genome-wide genotyping array 2018-11-02 28604731 Hammerschlag AR 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604731 Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Insomnia complaints 12,863 European ancestry male cases, 40,776 European ancestry male controls 1,983 Icelandic ancestry male cases, 1,791 Icelandic ancestry female cases, 2,064 Icelandic ancestry male controls, 1,727 Icelandic ancestry female controls Affymetrix [at least 12428592] (imputed) 2 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST006488 Genome-wide genotyping array 2017-09-14 28610988 Kerr KF 2017-06-10 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/28610988 Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts. Heart rate 13,184 Hispanic/Latino individuals 7,073 European ancestry individuals, 4,771 African American individuals Affymetrix, Illumina [16967914] (imputed) 2 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST004715 Genome-wide genotyping array 2017-09-14 28610988 Kerr KF 2017-06-10 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/28610988 Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts. Heart rate variability traits (RMSSD) 13,767 Hispanic/Latino individuals 4,730 European ancestry individuals, 2,908 African American individuals Affymetrix, Illumina [17209892] (imputed) 2 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST004716 Genome-wide genotyping array 2017-09-14 28610988 Kerr KF 2017-06-10 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/28610988 Genome-wide association study of heart rate and its variability in Hispanic/Latino cohorts. Heart rate variability traits (SDNN) 13,184 Hispanic/Latino individuals 7,073 European ancestry individuals, 2,908 African American individuals Affymetrix, Illumina [17209740] (imputed) 3 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST004714 Genome-wide genotyping array 2017-09-18 28604730 McKay JD 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604730 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Lung cancer 29,266 European ancestry cases, 56,450 European ancestry controls NA Illumina [10439017] (imputed) 135 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST004748 Genome-wide genotyping array 2017-09-18 28604730 McKay JD 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604730 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Lung adenocarcinoma 11,273 European ancestry cases, 55,483 European ancestry controls NA Illumina [10439017] (imputed) 79 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST004744 Genome-wide genotyping array 2017-09-18 28604730 McKay JD 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604730 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Squamous cell lung carcinoma 7,426 European ancestry cases, 55,627 European ancestry controls NA Illumina [10439017] (imputed) 101 squamous cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000708 GCST004750 Genome-wide genotyping array 2017-09-18 28604730 McKay JD 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604730 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Small cell lung carcinoma 2,664 European ancestry cases, 21,444 European ancestry controls NA Illumina [10439017] (imputed) 50 small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000702 GCST004746 Genome-wide genotyping array 2017-09-18 28604730 McKay JD 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604730 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Lung cancer in ever smokers 23,223 European ancestry cases, 16,964 European ancestry controls NA Illumina [10439017] (imputed) 111 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST004749 Genome-wide genotyping array 2017-09-18 28604730 McKay JD 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604730 Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes. Lung cancer in never smokers 2,355 European ancestry cases, 7,504 European ancestry controls NA Illumina [10439017] (imputed) 23 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST004747 Genome-wide genotyping array 2017-01-31 27436580 Cui Q 2016-07-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27436580 An extended genome-wide association study identifies novel susceptibility loci for nasopharyngeal carcinoma. Nasopharyngeal carcinoma 1,583 Southern Chinese ancestry cases, 2,979 Southern Chinese ancestry controls 5,463 Southern Chinese ancestry cases, 5,591 Southern Chinese ancestry controls Illumina [463250] 6 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST003578 Genome-wide genotyping array 2017-11-17 28922980 Konte B 2017-09-19 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28922980 A genome-wide association study of early gamma-band response in a schizophrenia case-control sample. Disturbances of the gamma-frequency band of electroencephalography measures in schizophrenia 74 European ancestry cases, 241 European ancestry controls NA Illumina [304635] 3 gamma wave measurement http://www.ebi.ac.uk/efo/EFO_0008388 GCST004953 Genome-wide genotyping array 2017-09-05 28632202 Witt SH 2017-06-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/28632202 Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia. Borderline personality disorder 998 European ancestry cases, 1,545 European ancestry controls NA Illumina [10736316] (imputed) 28 Borderline personality disorder http://purl.obolibrary.org/obo/HP_0012076 GCST004641 Genome-wide genotyping array 2017-07-21 28453389 Koga A 2017-04-28 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/28453389 GWAS analysis of treatment resistant schizophrenia: interaction effect of childhood trauma. Resistance to antipsychotic treatment in schizophrenia 31 European ancestry treatment-resistant cases, 53 European ancestry non-treatment-resistant controls NA Illumina [1178234] 0 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST004375 Genome-wide genotyping array 2017-07-21 28453389 Koga A 2017-04-28 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/28453389 GWAS analysis of treatment resistant schizophrenia: interaction effect of childhood trauma. Resistance to antipsychotic treatment in schizophrenia (childhood trauma interaction) 31 European ancestry treatment-resistant cases, 53 European ancestry non-treatment-resistant controls NA Illumina [1178234] 0 childhood trauma measurement, response to antipsychotic drug http://www.ebi.ac.uk/efo/EFO_0007979, http://purl.obolibrary.org/obo/GO_0097332 GCST004374 Genome-wide genotyping array 2017-09-11 28628665 Sobota RS 2017-06-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28628665 A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa. Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (continuous) 244 cases, 225 controls Illumina [542585] 4 tuberculin skin test reactivity measurement, decreased susceptibility to bacterial infection http://www.ebi.ac.uk/efo/EFO_0008307, http://www.ebi.ac.uk/efo/EFO_0008322 GCST004689 Genome-wide genotyping array 2017-09-11 28628665 Sobota RS 2017-06-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28628665 A chromosome 5q31.1 locus associates with tuberculin skin test reactivity in HIV-positive individuals from tuberculosis hyper-endemic regions in east Africa. Resistance to Mycobacterium tuberculosis in HIV-positive individuals measured by a negative tuberculin skin test (dichotomous) 244 cases, 225 controls Illumina [542585] 3 tuberculin skin test reactivity measurement, decreased susceptibility to bacterial infection http://www.ebi.ac.uk/efo/EFO_0008307, http://www.ebi.ac.uk/efo/EFO_0008322 GCST004690 Genome-wide genotyping array 2017-08-23 28630421 Li D 2017-06-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28630421 A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling. Anorexia nervosa (excluding migration to or from binge-eating disorder or bulimia nervosa) 692 European ancestry female cases and 3,570 European ancestry female controls Cases and controls (see Boraska et al, 2014) Illumina [507999] 1 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST004585 Genome-wide genotyping array 2017-12-20 29124805 Carlson JC 2017-11-10 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29124805 Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes. Orofacial clefts (cleft lip vs. cleft lip and palate) 56 African ancestry cleft lip cases, 121 Asian ancestry cleft lip cases, 128 European ancestry cleft lip cases, 145 Latin/South American cleft lip cases, 91 African ancestry cleft lip with cleft palate cases, 246 Asian ancestry cleft lip with cleft palate cases, 448 European ancestry cleft lip with cleft palate cases, 905 Latin/South American cleft lip with cleft palate cases, 2 cleft lip with cleft palate cases 176 Brazilian ancestry cleft lip cases, 168 Mongolian ancestry cleft lip cases, 16 Filipino ancestry cleft lip cases, 213 European ancestry cleft lip cases, 224 Asian ancestry cleft lip cases, 287 Brazilian ancestry cleft lip with cleft palate cases, 374 Mongolian ancestry cleft lip with cleft palate cases, 64 Filipino ancestry cleft lip with cleft palate cases, 385 European ancestry cleft lip with cleft palate cases, 703 Asian ancestry cleft lip with cleft palate cases. Illumina [10401483] (imputed) 0 Cleft palate, obsolete Mendelian syndromes with cleft lip/palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://purl.obolibrary.org/obo/MONDO_0015335, http://www.ebi.ac.uk/efo/EFO_0003959 GCST005079 Genome-wide genotyping array 2017-11-20 29051540 Marenholz I 2017-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29051540 Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy. Cow's milk allergy 169 European ancestry cases, 2,387 European ancestry controls 390 European ancestry cases, 2,510 European ancestry controls Illumina [5405832] (imputed) 0 milk allergy measurement http://www.ebi.ac.uk/efo/EFO_0007019 GCST004978 Genome-wide genotyping array 2017-11-20 29051540 Marenholz I 2017-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29051540 Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy. Food allergy 497 European ancestry cases, 2,387 European ancestry controls 1,050 European ancestry cases, 2,510 European ancestry controls Illumina [5405832] (imputed) 2 food allergy measurement http://www.ebi.ac.uk/efo/EFO_0007016 GCST004979 Genome-wide genotyping array 2017-11-20 29051540 Marenholz I 2017-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29051540 Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy. Peanut allergy 230 European ancestry cases, 2,387 European ancestry controls 438 European ancestry cases, 2,510 European ancestry controls Illumina [5405832] (imputed) 1 peanut allergy measurement http://www.ebi.ac.uk/efo/EFO_0007017 GCST004980 Genome-wide genotyping array 2017-11-20 29051540 Marenholz I 2017-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29051540 Genome-wide association study identifies the SERPINB gene cluster as a susceptibility locus for food allergy. Hen's egg allergy 288 European ancestry cases, 2,387 European ancestry controls 416 European ancestry cases, 2,510 European ancestry controls Illumina [5405832] (imputed) 2 egg allergy measurement http://www.ebi.ac.uk/efo/EFO_0007018 GCST004977 Genome-wide genotyping array 2018-11-30 29130521 Christopher L 2017-11-11 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/29130521 A variant in PPP4R3A protects against alzheimer-related metabolic decline. Decline in glucose metabolism in posterior cingulate cortex 335 European ancestry MCI cases, 79 European ancestry AD cases, 192 European ancestry controls NA Illumina [2820932] (imputed) 9 glucose metabolism decline measurement, cingulate cortex measurement http://www.ebi.ac.uk/efo/EFO_0009392, http://www.ebi.ac.uk/efo/EFO_0007738 GCST006632 Genome-wide genotyping array 2017-12-19 29058716 Milne RL 2017-10-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29058716 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Breast cancer (estrogen-receptor negative) 14,135 European ancestry cases, 58,126 European ancestry controls 7,333 European ancestry cases, 42,468 European ancestry controls Illumina [~ 11500000] (imputed) 46 estrogen-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_1000650 GCST005076 Genome-wide genotyping array 2017-12-19 29058716 Milne RL 2017-10-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29058716 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Breast cancer 14,135 European ancestry ER- cases, 58,126 European ancestry controls, 7,784 European ancestry BRCA1 carrrier cases, 7,782 European ancestry BRCA1 carrrier controls 7,333 European ancestry ER- cases, 42,468 European ancestry controls, 1,630 European ancestry BRCA1 carrrier cases, 1,712 European ancestry BRCA1 carrrier controls Illumina [~ 11500000] (imputed) 10 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST005077 Genome-wide genotyping array 2017-12-19 29058716 Milne RL 2017-10-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29058716 Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Breast Cancer in BRCA1 mutation carriers 7,784 European ancestry carrier cases, 7,782 European ancestry carrier controls 1,630 European ancestry carrier cases, 1,712 European ancestry carrier controls Illumina [~ 11500000] (imputed) 10 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST005075 Genome-wide genotyping array 2017-11-28 29066090 Allen RJ 2017-10-20 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/29066090 Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. Idiopathic pulmonary fibrosis 602 European ancestry cases, 3,366 European ancestry controls 2,158 cases, 5,195 controls Affymetrix [NR] (imputed) 8 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST004986 Genome-wide genotyping array 2017-12-05 29083406 Ferreira MA 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083406 Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Allergic disease (asthma, hay fever or eczema) 180,129 European ancestry cases, 180,709 European ancestry controls NA Affymetrix, Illumina [8307659] (imputed) 136 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST005038 Genome-wide genotyping array 2018-02-27 29292387 Turley P 2018-01-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29292387 Multi-trait analysis of genome-wide association summary statistics using MTAG. Depressive symptoms (MTAG) 354,862 European ancestry individuals NA Illumina [NR] (imputed) 64 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST005323 Genome-wide genotyping array 2018-02-27 29292387 Turley P 2018-01-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29292387 Multi-trait analysis of genome-wide association summary statistics using MTAG. Subjective well-being (MTAG) 388,538 European ancestry individuals NA Illumina [NR] (imputed) 49 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST005325 Genome-wide genotyping array 2018-02-27 29292387 Turley P 2018-01-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29292387 Multi-trait analysis of genome-wide association summary statistics using MTAG. Neuroticism (MTAG) 168,105 European ancestry individuals NA Illumina [NR] (imputed) 37 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST005326 Genome-wide genotyping array 2018-02-27 29292387 Turley P 2018-01-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29292387 Multi-trait analysis of genome-wide association summary statistics using MTAG. Neuroticism 168,105 European ancestry individuals NA Illumina [NR] (imputed) 12 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST005327 Genome-wide genotyping array 2018-02-27 29292387 Turley P 2018-01-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29292387 Multi-trait analysis of genome-wide association summary statistics using MTAG. Depressive symptoms 354,862 European ancestry individuals NA Illumina [NR] (imputed) 32 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST005324 Genome-wide genotyping array 2018-02-27 29292387 Turley P 2018-01-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29292387 Multi-trait analysis of genome-wide association summary statistics using MTAG. Subjective well-being 388,538 European ancestry individuals NA Illumina [NR] (imputed) 13 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST005328 Genome-wide genotyping array 2017-09-14 28604732 Wang Z 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604732 Meta-analysis of five genome-wide association studies identifies multiple new loci associated with testicular germ cell tumor. Testicular germ cell tumor 3,558 European ancestry cases, 13,970 European ancestry controls NA Illumina [9210350] (imputed) 37 Testicular Germ Cell Tumor http://www.ebi.ac.uk/efo/EFO_1000566 GCST004713 Genome-wide genotyping array 2017-09-15 28613276 Nolte IM 2017-06-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28613276 Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Heart rate variability traits (SDNN) 27,850 European ancestry individuals 24,125 European ancestry individuals, 11,234 Hispanic/Latino individuals, 6,899 African American individuals Affymetrix, Illumina, Perlegen [at least 2135543] (imputed) 23 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST004734 Genome-wide genotyping array 2017-09-15 28613276 Nolte IM 2017-06-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28613276 Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Heart rate variability traits (RMSSD) 26,523 European ancestry individuals 20,429 European ancestry individuals, 11,234 Hispanic/Latino individuals, 6,895 African American individuals Affymetrix, Illumina, Perlegen [at least 2135543] (imputed) 22 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST004733 Genome-wide genotyping array 2017-09-15 28613276 Nolte IM 2017-06-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28613276 Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Heart rate variability traits (pvRSA/HF) 24,088 European ancestry individuals 9,377 European ancestry individuals, 404 Hispanic/Latino individuals, 1,901 African American individuals Affymetrix, Illumina, Perlegen [at least 2135543] (imputed) 12 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST004732 Genome-wide genotyping array 2018-01-15 29228715 Hofer P 2017-10-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29228715 Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Colorectal cancer 978 Austrian ancestry colorectal cancer cases, 636 Austrian ancestry advanced colorectal adenoma cases, , 855 Austrian ancestry controls NA Affymetrix [492217] (imputed) 6 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST005148 Genome-wide genotyping array 2018-01-15 29228715 Hofer P 2017-10-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29228715 Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Colorectal cancer 978 Austrian ancestry cases, 4,294 European ancestry controls NA Affymetrix [492217] (imputed) 42 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST005149 Genome-wide genotyping array 2018-01-15 29228715 Hofer P 2017-10-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29228715 Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Colorectal cancer 978 Austrian ancestry colorectal cancer cases, 636 Austrian ancestry advanced colorectal adenoma cases, 4,294 European ancestry controls NA Affymetrix [492217] (imputed) 42 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST005150 Genome-wide genotyping array 2018-01-15 29228715 Hofer P 2017-10-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29228715 Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Colorectal adenoma (advanced) 636 Austrian ancestry cases, 4,294 European ancestry controls NA Affymetrix [492217] (imputed) 21 colorectal adenoma http://www.ebi.ac.uk/efo/EFO_0005406 GCST005151 Genome-wide genotyping array 2018-01-15 29228715 Hofer P 2017-10-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29228715 Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Colorectal cancer 978 Austrian ancestry cases, 855 Austrian ancestry controls NA Affymetrix [492217] (imputed) 13 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST005152 Genome-wide genotyping array 2018-01-15 29228715 Hofer P 2017-10-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29228715 Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Colorectal adenoma (advanced) 636 Austrian ancestry cases, 855 Austrian ancestry controls NA Affymetrix [492217] (imputed) 9 colorectal adenoma http://www.ebi.ac.uk/efo/EFO_0005406 GCST005153 Genome-wide genotyping array 2018-01-15 29228715 Hofer P 2017-10-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29228715 Bayesian and frequentist analysis of an Austrian genome-wide association study of colorectal cancer and advanced adenomas. Colonoscopy-negative controls vs population controls 855 Austrian ancestry colonoscopy-negative controls, 3,439 European ancestry controls NA Affymetrix [492217] (imputed) 131 colorectal health http://www.ebi.ac.uk/efo/EFO_0008460 GCST005147 Genome-wide genotyping array 2017-10-23 28931804 Benyamin B 2017-09-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28931804 Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis (sporadic) 1,234 Chinese ancestry cases, 2,850 Chinese ancestry controls, 12,577 European ancestry cases, 23,475 European ancestry controls 576 cases, 683 controls Illumina [at least 6613544] (imputed) 4 sporadic amyotrophic lateral sclerosis http://www.ebi.ac.uk/efo/EFO_0001357 GCST004901 Genome-wide genotyping array 2019-08-20 28931804 Benyamin B 2017-09-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28931804 Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis (sporadic) 1,234 Chinese ancestry cases, 2,850 Chinese ancestry controls, 12,577 European ancestry cases, 23,475 European ancestry controls 576 cases, 683 controls Illumina [at least 6613544] (imputed) 0 sporadic amyotrophic lateral sclerosis http://www.ebi.ac.uk/efo/EFO_0001357 GCST008472 Genome-wide genotyping array 2017-10-05 28840121 Villalobos-Comparan M 2017-08-03 Int J Genomics www.ncbi.nlm.nih.gov/pubmed/28840121 A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density. Femoral neck bone geometry 411 Mexican ancestry women 420 Mexican ancestry women Illumina [225635] 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST004835 Genome-wide genotyping array 2017-10-05 28840121 Villalobos-Comparan M 2017-08-03 Int J Genomics www.ncbi.nlm.nih.gov/pubmed/28840121 A Pilot Genome-Wide Association Study in Postmenopausal Mexican-Mestizo Women Implicates the RMND1/CCDC170 Locus Is Associated with Bone Mineral Density. Lumbar spine bone mineral density 411 Mexican ancestry women 420 Mexican ancestry women Illumina [225635] 0 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST004834 Genome-wide genotyping array 2017-10-06 28598419 Hong X 2017-06-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28598419 Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth. Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) 329 African American normal weight preterm birth mothers, 514 African American normal weight term birth mothers, 463 African American overweight or obese preterm birth mothers, 580 African American overweight or obese term birth mothers NA Affymetrix, Illumina [9929081] (imputed) 1 body mass index, premature birth, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0003917, http://www.ebi.ac.uk/efo/EFO_0005939 GCST004842 Genome-wide genotyping array 2017-10-06 28598419 Hong X 2017-06-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28598419 Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth. Preterm birth (maternal effect) 698 African American preterm birth mothers, 1,035 African American term birth mothers 307 African American preterm birth mothers, 475 African American term birth mothers, 318 European ancestry preterm birth mothers, 365 European ancestry term birth mothers Illumina [13317377] (imputed) 0 premature birth, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0003917, http://www.ebi.ac.uk/efo/EFO_0005939 GCST004841 Genome-wide genotyping array 2017-10-06 28598419 Hong X 2017-06-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28598419 Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth. Spontaneous preterm birth (maternal effect) 461 African American spontaneous preterm birth mothers, 1,035 African American term birth mothers NA Illumina [13317377] (imputed) 2 spontaneous preterm birth, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0006917, http://www.ebi.ac.uk/efo/EFO_0005939 GCST004845 Genome-wide genotyping array 2017-10-06 28598419 Hong X 2017-06-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28598419 Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth. Gestational age at birth (maternal effect) 698 African American preterm birth mothers, 1,035 African American term birth mothers NA Illumina [13317377] (imputed) 3 gestational age, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0005939 GCST004844 Genome-wide genotyping array 2017-10-06 28598419 Hong X 2017-06-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28598419 Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth. Preterm birth (maternal effect) (maternal pre-pregnancy BMI interaction) 447 African American normal weight term birth mothers, 498 African American overweight or obese term birth mothers, 268 African American normal weight preterm birth mothers, 373 African American overweight or obese preterm birth mothers 67 African American normal weight term birth mothers, 82 African American overweight or obese term birth mothers, 61 African American normal weight preterm birth mothers, 90 African American overweight or obese preterm birth mothers, 247 European ancestry normal weight term birth mothers, 118 European ancestry overweight or obese term birth mothers, 192 European ancestry normal weight preterm birth mothers, 126 European ancestry overweight or obese preterm birth mothers Illumina [13317377] (imputed) 0 body mass index, premature birth, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0003917, http://www.ebi.ac.uk/efo/EFO_0005939 GCST004843 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Chickenpox 107,769 European ancestry cases, 15,982 European ancestry controls NA Illumina [at least 560000] (imputed) 36 susceptibility to chickenpox measurement http://www.ebi.ac.uk/efo/EFO_0008400 GCST004999 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Shingles 16,711 European ancestry cases, 118,152 European ancestry controls NA Illumina [at least 560000] (imputed) 75 susceptibility to shingles measurement http://www.ebi.ac.uk/efo/EFO_0008401 GCST005001 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Cold sores 25,108 European ancestry cases, 63,332 European ancestry controls NA Illumina [at least 560000] (imputed) 49 susceptibility to cold sores measurement http://www.ebi.ac.uk/efo/EFO_0008402 GCST005000 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Bacterial meningitis 842 European ancestry cases, 82,778 European ancestry controls NA Illumina [at least 560000] (imputed) 38 susceptibility to bacterial meningitis measurement http://www.ebi.ac.uk/efo/EFO_0008411 GCST005010 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Yeast infection 52,218 European ancestry cases, 10,235 European ancestry controls NA Illumina [at least 560000] (imputed) 51 susceptibility to vaginal yeast infection measurement http://www.ebi.ac.uk/efo/EFO_0008412 GCST005011 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Myringotomy 4,138 European ancestry cases, 85,089 European ancestry controls NA Illumina [at least 560000] (imputed) 34 susceptibility to childhood ear infection measurement http://www.ebi.ac.uk/efo/EFO_0007904 GCST005015 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Number of common colds 43,826 European ancestry cases, 15,720 European ancestry controls NA Illumina [at least 560000] (imputed) 34 susceptibility to common cold measurement http://www.ebi.ac.uk/efo/EFO_0008417 GCST005019 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Chronic sinus infection 5,291 European ancestry cases, 79,622 European ancestry controls NA Illumina [at least 560000] (imputed) 45 susceptibility to chronic sinus infection measurement http://www.ebi.ac.uk/efo/EFO_0008419 GCST005021 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Urinary tract infection frequency 35,000 European ancestry cases, 33,478 European ancestry controls NA Illumina [at least 560000] (imputed) 61 susceptibility to urinary tract infection measurement http://www.ebi.ac.uk/efo/EFO_0008413 GCST005012 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Tonsillectomy 60,098 European ancestry cases, 113,323 European ancestry controls NA Illumina [at least 560000] (imputed) 204 tonsillectomy risk measurement http://www.ebi.ac.uk/efo/EFO_0007924 GCST005014 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Mumps 31,227 European ancestry cases, 54,153 European ancestry controls NA Illumina [at least 560000] (imputed) 55 susceptibility to mumps measurement http://www.ebi.ac.uk/efo/EFO_0008404 GCST005003 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Plantar warts 24,994 European ancestry cases, 37,451 European ancestry controls NA Illumina [at least 560000] (imputed) 81 susceptibility to plantar warts measurement http://www.ebi.ac.uk/efo/EFO_0008406 GCST005005 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Tuberculosis 4,426 European ancestry cases, 84,290 European ancestry controls NA Illumina [at least 560000] (imputed) 67 susceptibility to Mycobacterium tuberculosis infection measurement http://www.ebi.ac.uk/efo/EFO_0008407 GCST005006 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Measles 38,219 European ancestry cases, 47,279 European ancestry controls NA Illumina [at least 560000] (imputed) 32 susceptibility to measles measurement http://www.ebi.ac.uk/efo/EFO_0008414 GCST005016 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Hepatitis A 2,442 European ancestry cases, 217,137 European ancestry controls NA Illumina [at least 560000] (imputed) 36 susceptibility to hepatitis A infection measurement http://www.ebi.ac.uk/efo/EFO_0008415 GCST005017 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Rheumatic fever 1,115 European ancestry cases, 88,076 European ancestry controls NA Illumina [at least 560000] (imputed) 24 susceptibility to rheumatic fever measurement http://www.ebi.ac.uk/efo/EFO_0008416 GCST005018 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Childhood ear infection 46,936 European ancestry cases, 74,874 European ancestry controls NA Illumina [at least 560000] (imputed) 102 susceptibility to childhood ear infection measurement http://www.ebi.ac.uk/efo/EFO_0007904 GCST005013 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Rubella 12,000 European ancestry cases, 71,597 European ancestry controls NA Illumina [at least 560000] (imputed) 38 susceptibility to rubella infection measurement http://www.ebi.ac.uk/efo/EFO_0008418 GCST005020 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Mononucleosis 17,457 European ancestry cases, 68,446 European ancestry controls NA Illumina [at least 560000] (imputed) 44 susceptibility to mononucleosis measurement http://www.ebi.ac.uk/efo/EFO_0008403 GCST005002 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Hepatitis B 1,425 European ancestry cases, 218,180 European ancestry controls NA Illumina [at least 560000] (imputed) 39 susceptibility to hepatitis B infection measurement http://www.ebi.ac.uk/efo/EFO_0008405 GCST005004 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Strep throat 52,487 European ancestry cases, 22,017 European ancestry controls NA Illumina [at least 560000] (imputed) 53 susceptibility to strep throat measurement http://www.ebi.ac.uk/efo/EFO_0008408 GCST005007 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Scarlet fever 6,812 European ancestry cases, 113,837 European ancestry controls NA Illumina [at least 560000] (imputed) 59 susceptibility to scarlet fever measurement http://www.ebi.ac.uk/efo/EFO_0008409 GCST005008 Genome-wide genotyping array 2017-12-01 28928442 Tian C 2017-09-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28928442 Genome-wide association and HLA region fine-mapping studies identify susceptibility loci for multiple common infections. Pneumonia 40,600 European ancestry cases, 90,039 European ancestry controls NA Illumina [at least 560000] (imputed) 67 susceptibility to pneumonia measurement http://www.ebi.ac.uk/efo/EFO_0008410 GCST005009 Genome-wide genotyping array 2018-03-29 29358691 Bonas-Guarch S 2018-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29358691 Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Type 2 diabetes up to 12,931 European ancestry cases, up to 57,196 European ancestry controls NA Affymetrix, Illumina [~ 13000000] (imputed) 20 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST005413 Genome-wide genotyping array 2018-07-16 29358691 Bonas-Guarch S 2018-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29358691 Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Type 2 diabetes 7,522 European ancestry cases, 50,446 European ancestry controls 35,789 African-American, East Asian, South Asian, European or Hispanic cases, 56,738 African-American, East Asian, South Asian, European or Hispanic controls Affymetrix, Illumina [1918233] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST005899 Exome genotyping array [Exome array] 2018-07-16 29358691 Bonas-Guarch S 2018-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29358691 Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Type 2 diabetes 5,277 European ancestry cases, 15,702 European ancestry controls 9,253 European ancestry cases and controls, 3,490 Hispanic case and controls, 174,532 cases and controls Affymetrix, Illumina [~ 1000000] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST005898 Genome-wide genotyping array 2017-07-06 28452372 Gorski M 2017-04-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28452372 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Glomerular filtration rate (cystatin C) 24,063 European ancestry individuals Affymetrix, Illumina [up to 10971307] (imputed) 3 glomerular filtration rate, cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0004617 GCST004293 Genome-wide genotyping array 2017-07-06 28452372 Gorski M 2017-04-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28452372 1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function. Glomerular filtration rate (creatinine) 110,517 European ancestry individuals Affymetrix, Illumina [up to 10971307] (imputed) 57 creatinine measurement, glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0005208 GCST004292 Genome-wide genotyping array 2018-03-29 29358691 Bonas-Guarch S 2018-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29358691 Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes. Type 2 diabetes 19,693 European ancestry cases, 107,308 European ancestry controls, 6,952 East Asian ancestry cases, 11,865 East Asian ancestry controls, 5,561 South Asian ancestry cases, 14,458 South Asian ancestry controls, 1,804 Mexican ancestry cases, 779 Mexican ancestry controls Affymetrix, Illumina [1918233] (imputed) 24 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST005414 Genome-wide genotyping array 2018-01-12 29112194 Agrawal A 2017-11-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29112194 Genome-wide association study identifies a novel locus for cannabis dependence. Cannabis dependence symptom count 8,050 European ancestry individuals NA Illumina [at least 4916924] (imputed) 7 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST005128 Genome-wide genotyping array 2018-01-12 29112194 Agrawal A 2017-11-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29112194 Genome-wide association study identifies a novel locus for cannabis dependence. Cannabis dependence 2,080 European ancestry cases, 6,435 European ancestry controls 781 European ancestry cases, 1,591 European ancestry controls, 896 African American cases, 1,905 African American controls Illumina [at least 4916924] (imputed) 1 cannabis dependence http://www.ebi.ac.uk/efo/EFO_0007191 GCST005133 Genome-wide genotyping array 2017-11-06 28918882 Wattacheril J 2017-09-14 J Pediatr www.ncbi.nlm.nih.gov/pubmed/28918882 Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys. Pediatric non-alcoholic fatty liver disease activity score 208 Hispanic boys NA Illumina [up to 624297] 1 non-alcoholic fatty liver disease severity measurement http://www.ebi.ac.uk/efo/EFO_0008421 GCST004942 Genome-wide genotyping array 2017-11-06 28918882 Wattacheril J 2017-09-14 J Pediatr www.ncbi.nlm.nih.gov/pubmed/28918882 Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys. Liver fibrosis in pediatric non-alcoholic fatty acid liver disease 208 Hispanic boys NA Illumina [up to 624297] 5 Hepatic fibrosis http://purl.obolibrary.org/obo/HP_0001395 GCST004938 Genome-wide genotyping array 2017-11-06 28918882 Wattacheril J 2017-09-14 J Pediatr www.ncbi.nlm.nih.gov/pubmed/28918882 Genome-Wide Associations Related to Hepatic Histology in Nonalcoholic Fatty Liver Disease in Hispanic Boys. Pediatric nonalcoholic steatohepatitis 46 Hispanic boy definite NASH cases, 110 Hispanic boy borderline NASH controls NA Illumina [up to 624297] 2 non-alcoholic steatohepatitis http://www.ebi.ac.uk/efo/EFO_1001249 GCST004943 Genome-wide genotyping array 2017-11-20 28921760 Chenoweth MJ 2017-09-16 Addiction www.ncbi.nlm.nih.gov/pubmed/28921760 Genome-wide association study of a nicotine metabolism biomarker in African American smokers: impact of chromosome 19 genetic influences. Nicotine metabolite ratio in current smokers 954 African American individuals 480 African American individuals Illumina [at least 17919969] (imputed) 3 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST004976 Genome-wide genotyping array 2017-11-03 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG sialylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 7 IgG sialylation measurement http://www.ebi.ac.uk/efo/EFO_0008428 GCST004930 Genome-wide genotyping array 2017-11-03 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG disialylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 4 IgG disialylation measurement http://www.ebi.ac.uk/efo/EFO_0008429 GCST004931 Genome-wide genotyping array 2017-11-03 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG monosialylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 3 IgG monosialylation measurement http://www.ebi.ac.uk/efo/EFO_0008430 GCST004932 Genome-wide genotyping array 2017-11-02 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG fucosylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 7 IgG fucosylation measurement http://www.ebi.ac.uk/efo/EFO_0008427 GCST004929 Genome-wide genotyping array 2017-11-02 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG bisecting N-acetyl glucosamine phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 5 IgG bisecting N-acetyl glucosamine measurement http://www.ebi.ac.uk/efo/EFO_0008426 GCST004928 Genome-wide genotyping array 2017-11-02 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG galactosylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 9 IgG galactosylation measurement http://www.ebi.ac.uk/efo/EFO_0008425 GCST004927 Genome-wide genotyping array 2017-11-02 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG monogalactosylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 6 IgG monogalactosylation measurement http://www.ebi.ac.uk/efo/EFO_0008423 GCST004924 Genome-wide genotyping array 2017-11-02 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG digalactosylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 6 IgG digalactosylation measurement http://www.ebi.ac.uk/efo/EFO_0008424 GCST004926 Genome-wide genotyping array 2017-11-02 28878392 Shen X 2017-09-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28878392 Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation. IgG N-glycosylation phenotypes (multivariate analysis) 1,960 Orcadian (founder/genetic isolate) individuals NA Illumina [NR] 9 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST004925 Genome-wide genotyping array 2018-02-20 29385134 Kawaguchi T 2018-01-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/29385134 Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. Nonalcoholic steatohepatitis-derived hepatocellular carcinoma 58 Japanese ancestry cases, 7,672 Japanese ancestry controls NA Illumina [93606] 3 hepatocellular carcinoma, non-alcoholic steatohepatitis http://www.ebi.ac.uk/efo/EFO_0000182, http://www.ebi.ac.uk/efo/EFO_1001249 GCST005309 Genome-wide genotyping array 2018-02-20 29385134 Kawaguchi T 2018-01-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/29385134 Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. Brunt stage in nonalcoholic fatty liver disease 474 Japanese ancestry cases NA Illumina [93606] 0 non-alcoholic fatty liver disease severity measurement http://www.ebi.ac.uk/efo/EFO_0008421 GCST005307 Genome-wide genotyping array 2018-02-20 29385134 Kawaguchi T 2018-01-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/29385134 Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. Brunt grade in nonalcoholic fatty liver disease 567 Japanese ancestry cases NA Illumina [93606] 0 non-alcoholic fatty liver disease severity measurement http://www.ebi.ac.uk/efo/EFO_0008421 GCST005310 Genome-wide genotyping array 2018-02-20 29385134 Kawaguchi T 2018-01-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/29385134 Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. Hepatocyte fat droplet content in nonalcoholic fatty liver disease 834 Japanese ancestry cases NA Illumina [93606] 0 non-alcoholic fatty liver disease severity measurement http://www.ebi.ac.uk/efo/EFO_0008421 GCST005311 Genome-wide genotyping array 2018-02-20 29385134 Kawaguchi T 2018-01-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/29385134 Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers. Nonalcoholic fatty liver disease 902 Japanese ancestry cases, 7,672 Japanese ancestry controls NA Illumina [93606] 7 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST005308 Genome-wide genotyping array 2017-09-05 28588231 Li M 2017-06-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28588231 Genome-wide association study of 1,5-anhydroglucitol identifies novel genetic loci linked to glucose metabolism. 1,5-anhydroglucitol levels 7,550 European ancestry individuals 8,790 European ancestry individuals, 2,030 African American individuals Affymetrix [at least 8500000] (imputed) 8 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST004643 Genome-wide genotyping array 2018-01-30 29212900 Li C 2017-12-06 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29212900 Genome-Wide Gene-Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity). Pulse pressure (dietary potassium intake interaction) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 0 pulse pressure measurement, dietary potassium intake measurement http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0008470 GCST005201 Genome-wide genotyping array 2018-01-30 29212900 Li C 2017-12-06 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29212900 Genome-Wide Gene-Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity). Systolic blood pressure (dietary potassium intake interaction) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 1 systolic blood pressure, dietary potassium intake measurement http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0008470 GCST005204 Genome-wide genotyping array 2018-01-30 29212900 Li C 2017-12-06 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29212900 Genome-Wide Gene-Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity). Diastolic blood pressure (dietary potassium intake interaction) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 0 diastolic blood pressure, dietary potassium intake measurement http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0008470 GCST005202 Genome-wide genotyping array 2018-01-30 29212900 Li C 2017-12-06 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29212900 Genome-Wide Gene-Potassium Interaction Analyses on Blood Pressure: The GenSalt Study (Genetic Epidemiology Network of Salt Sensitivity). Mean arterial pressure (dietary potassium intake interaction) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 0 mean arterial pressure, dietary potassium intake measurement http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0008470 GCST005203 Genome-wide genotyping array 2017-09-15 28608620 Coleman JRI 2017-06-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28608620 Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders. Facial emotion recognition 4,097 European ancestry individuals NA Illumina [2487351] (imputed) 3 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST004727 Genome-wide genotyping array 2017-09-15 28608620 Coleman JRI 2017-06-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28608620 Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders. Facial emotion recognition (happy faces) 4,097 European ancestry individuals NA Illumina [2487351] (imputed) 1 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST004729 Genome-wide genotyping array 2017-09-15 28608620 Coleman JRI 2017-06-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28608620 Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders. Facial emotion recognition (sad faces) 4,097 European ancestry individuals NA Illumina [2487351] (imputed) 4 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST004730 Genome-wide genotyping array 2017-09-15 28608620 Coleman JRI 2017-06-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28608620 Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders. Facial emotion recognition (angry faces) 4,097 European ancestry individuals NA Illumina [2487351] (imputed) 4 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST004728 Genome-wide genotyping array 2017-09-15 28608620 Coleman JRI 2017-06-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28608620 Genome-wide association study of facial emotion recognition in children and association with polygenic risk for mental health disorders. Facial emotion recognition (fearful faces) 4,097 European ancestry individuals NA Illumina [2487351] (imputed) 2 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST004731 Genome-wide genotyping array 2017-10-13 24097067 Lessard CJ 2013-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097067 Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. Sjögren's syndrome 395 European ancestry cases, 1,975 European ancestry controls 1,243 European ancestry cases, 4,779 European ancestry controls Illumina [648937] 15 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST004878 Genome-wide genotyping array 2017-10-13 24097067 Lessard CJ 2013-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097067 Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. Sjögren's syndrome 395 European ancestry cases, 1,975 European ancestry controls 1,158 European ancestry cases, 3,071 European ancestry controls Illumina [648937] 3 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST004879 Genome-wide genotyping array 2018-04-25 24097067 Lessard CJ 2013-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097067 Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. Sjögren's syndrome 1,541 European ancestry cases, 2,634 European ancestry controls NA Illumina [102585] 6 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST005532 Targeted genotyping array [ImmunoChip] 2018-08-03 28921602 Lee MH 2017-09-16 Hepatology www.ncbi.nlm.nih.gov/pubmed/28921602 Human leukocyte antigen variants and risk of hepatocellular carcinoma modified by hepatitis C virus genotypes: A genome-wide association study. Hepatocellular carcinoma in hepatitis C infection 502 Chinese ancestry cases, 749 Chinese ancestry controls 669 Chinese ancestry cases, 429 Chinese ancestry controls Affymetrix [576032] 1 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST006037 Genome-wide genotyping array 2018-08-03 28927820 Sugier PE 2017-09-16 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/28927820 A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions. Atopy 925 European ancestry cases, 735 European ancestry controls 641 French Canadian (founder/population isolate) cases, 497 French Canadian (founder/population isolate) controls, 106 cases, 340 controls Illumina [501167] 2 atopy http://www.ebi.ac.uk/efo/EFO_0002686 GCST006040 Genome-wide genotyping array 2017-10-16 28924153 Chang X 2017-09-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28924153 Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk. Neuroblastoma (11q deletion) 113 European ancestry cases, 5,109 European ancestry controls 44 European ancestry cases, 1,902 European ancestry controls Illumina [NR] 1 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST004883 Genome-wide genotyping array 2017-10-16 28924153 Chang X 2017-09-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28924153 Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk. Neuroblastoma (11q deletion vs 11q undeleted and MYCN amplification) 113 European ancestry 11q-deletion neuroblastoma cases, 78 European ancestry 11q-undeleted neuroblastoma cases, 204 European ancestry MYCN-amplification neuroblastoma cases NA Illumina [NR] 0 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST004882 Genome-wide genotyping array 2017-10-16 28924153 Chang X 2017-09-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28924153 Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk. Neuroblastoma (MYCN amplification) 260 European ancestry cases, 5,109 European ancestry controls NA Illumina [NR] 2 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST004885 Genome-wide genotyping array 2017-10-16 28924153 Chang X 2017-09-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28924153 Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk. Neuroblastoma (1p deletion) 69 European ancestry cases, 5,109 European ancestry controls NA Illumina [NR] 1 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST004884 Genome-wide genotyping array 2017-09-13 28598434 Scelo G 2017-06-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28598434 Genome-wide association study identifies multiple risk loci for renal cell carcinoma. Renal cell carcinoma 10,784 European ancestry cases, 20,406 European ancestry controls 3,182 European ancestry cases, 6,301 European ancestry controls Illumina [7437091] (imputed) 26 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST004710 Genome-wide genotyping array 2017-08-16 28540026 Anney RJL 2017-05-22 Mol Autism www.ncbi.nlm.nih.gov/pubmed/28540026 Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Autism spectrum disorder or schizophrenia schizophrenia cases and controls (see Ripke, 2014), up to 6,197 European ancestry ASD cases, up to 7,377 European ancestry controls, up to 1,190 ASD cases, up to 1,190 controls NA Affymetrix, Illumina [NR] 301 autism spectrum disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090 GCST004521 Genome-wide genotyping array 2017-08-16 28540026 Anney RJL 2017-05-22 Mol Autism www.ncbi.nlm.nih.gov/pubmed/28540026 Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. Autism spectrum disorder 6,197 European ancestry cases, 7,377 European ancestry controls, 1,190 cases, 1,190 controls 8,266 European ancestry cases, 147,562 European ancestry controls, 886 cases, 1,105 controls Affymetrix, Illumina [6695386] (imputed) 3 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST004520 Genome-wide genotyping array 2018-01-30 29196614 Sud A 2017-12-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29196614 Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Nodular sclerosis Hodgkin lymphoma 1,278 European ancestry cases, 14,325 European ancestry controls 1,586 cases, 3,069 controls Illumina [> 10000000] (imputed) 9 nodular sclerosis Hodgkin lymphoma http://www.ebi.ac.uk/efo/EFO_0004708 GCST005211 Genome-wide genotyping array 2018-01-30 29196614 Sud A 2017-12-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29196614 Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Mixed cellularity Hodgkin lymphoma 828 European ancestry cases, 14,315 European ancestry controls 135 cases, 3,069 controls Illumina [> 10000000] (imputed) 3 Hodgkins lymphoma, mixed cellularity http://www.ebi.ac.uk/efo/EFO_1002031 GCST005210 Genome-wide genotyping array 2018-01-30 29196614 Sud A 2017-12-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29196614 Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility. Hodgkin's lymphoma 3,077 European ancestry cases, 13,680 European ancestry controls 2,237 cases, 3,069 controls Illumina [> 10000000] (imputed) 6 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST005209 Genome-wide genotyping array 2017-10-13 28916551 Liu Y 2017-09-15 J Rheumatol www.ncbi.nlm.nih.gov/pubmed/28916551 Genetic Determinants of Radiographic Knee Osteoarthritis in African Americans. Knee osteoarthritis 742 African American cases, 475 African American controls NA Illumina [8300000] (imputed) 6 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST004881 Genome-wide genotyping array 2018-08-30 28941034 Smith CE 2017-09-21 Mol Nutr Food Res www.ncbi.nlm.nih.gov/pubmed/28941034 Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent. BMI x dairy intake interaction (1df interaction test) up to 25,513 European ancestry individuals up to 17,675 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 0 energy intake, body mass index http://www.ebi.ac.uk/efo/EFO_0003939, http://www.ebi.ac.uk/efo/EFO_0004340 GCST006173 Genome-wide genotyping array 2017-10-17 28937693 Clarke TK 2017-07-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28937693 Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117). Alcohol consumption 59,088 European ancestry females, 53,029 European ancestry males NA Affymetrix [12489781] (imputed) 20 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST004886 Genome-wide genotyping array 2017-10-17 28937693 Clarke TK 2017-07-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28937693 Genome-wide association study of alcohol consumption and genetic overlap with other health-related traits in UK Biobank (N=112 117). Alcohol consumption in current drinkers 108,309 European ancestry individuals NA Affymetrix [12489781] (imputed) 8 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST004887 Genome-wide genotyping array 2018-02-21 26414677 Day FR 2015-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26414677 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Menopause (age at onset) up to 69,626 European ancestry women NA Affymetrix, Illumina [~ 2600000] (imputed) 51 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST005312 Genome-wide genotyping array 2018-05-02 26414677 Day FR 2015-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26414677 Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair. Menopause (age at onset) up to 2,545 European ancestry women up to 46,638 European ancestry women Illumina [Exome array] 2 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST005560 Genome-wide genotyping array, Exome genotyping array [Exome array] 2016-09-23 26502338 Bentham J 2015-10-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26502338 Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. Systemic lupus erythematosus 5,201 European ancestry cases, 9,066 European ancestry controls NA Illumina [> 644674] (imputed) 47 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST003156 Genome-wide genotyping array 2016-09-23 26502338 Bentham J 2015-10-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26502338 Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus. Systemic lupus erythematosus 5,201 European ancestry cases, 9,066 European ancestry controls 2,018 European ancestry cases, 6,925 European ancestry controls Illumina [644674] 53 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST003155 Genome-wide genotyping array 2017-07-20 22833209 Hu X 2011-11-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/22833209 Genome-wide association study identifies multiple novel loci associated with disease progression in subjects with mild cognitive impairment. Rate of cognitive decline in mild cognitive impairment (time interaction) 822 European ancestry individuals NA Illumina [233603] 3 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST004371 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Waist circumference 1,254 whole genome sequenced European ancestry individuals, 3,072 whole genome sequenced individuals, 41,450 European ancestry individuals, 397 Carlantino (founder/genetic isolate) individuals, 791 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,060 Mylopotamos (founder/genetic isolate) individuals, 887 Pomak (founder/genetic isolate) individuals, 1,754 Val Borbera (founder/genetic isolate) individuals 206,737 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 118 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST008151 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Weight 1,249 whole genome sequenced European ancestry individuals, 3,559 whole genome sequenced individuals, 46,819 European ancestry individuals, 472 Carlantino (founder/genetic isolate) individuals, 1,172 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,051 Mylopotamos (founder/genetic isolate) individuals, 942 Pomak (founder/genetic isolate) individuals, 1,779 Val Borbera (founder/genetic isolate) individuals 179,022 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 200 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST008152 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Lean body mass 3,399 whole genome sequenced individuals, 11,801 European ancestry individuals 10,676 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 76 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST008153 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Trunk fat mass 3,399 whole genome sequenced individuals, 12,838 European ancestry individuals 10,667 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 79 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST008154 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Waist-hip ratio 1,254 whole genome sequenced European ancestry individuals, 3,071 whole genome sequenced individuals, 29,723 European ancestry individuals, 388 Carlantino (founder/genetic isolate) individuals, 791 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,053 Mylopotamos (founder/genetic isolate) individuals, 879 Pomak (founder/genetic isolate) individuals 206,053 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 80 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008155 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Hip circumference adjusted for BMI 1,247 whole genome sequenced European ancestry individuals, 3,052 whole genome sequenced individuals, 29,518 European ancestry individuals, 400 Carlantino (founder/genetic isolate) individuals, 831 Friuli Venezia Giulia (founder/genetic isolate) individuals, 998 Mylopotamos (founder/genetic isolate) individuals, 871 Pomak (founder/genetic isolate) individuals 205,905 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 148 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST008156 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Height 1,249 whole genome sequenced European ancestry individuals, 3,541 whole genome sequenced individuals, 46,910 European ancestry individuals, 471 Carlantino (founder/genetic isolate) individuals, 1,197 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,043 Mylopotamos (founder/genetic isolate) individuals, 933 Pomak (founder/genetic isolate) individuals, 1,785 Val Borbera (founder/genetic isolate) individuals 205,003 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 630 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST008163 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Body fat mass 3,399 whole genome sequenced individuals, 11,802 European ancestry individuals 10,670 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 73 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST008157 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Body mass index 1,249 whole genome sequenced European ancestry individuals, 3,538 whole genome sequenced individuals, 46,635 European ancestry individuals, 472 Carlantino (founder/genetic isolate) individuals, 1,170 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,019 Mylopotamos (founder/genetic isolate) individuals, 932 Pomak (founder/genetic isolate) individuals, 1,778 Val Borbera (founder/genetic isolate) individuals 209,191 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 153 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008158 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Waist-to-hip ratio adjusted for BMI 1,247 whole genome sequenced European ancestry individuals, 3,049 whole genome sequenced individuals, 29,518 European ancestry individuals, 388 Carlantino (founder/genetic isolate) individuals, 790 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,001 Mylopotamos (founder/genetic isolate) individuals, 867 Pomak (founder/genetic isolate) individuals 206,045 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 85 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST008159 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Waist circumference adjusted for body mass index 1,247 whole genome sequenced European ancestry individuals, 3,050 whole genome sequenced individuals, 41,027 European ancestry individuals, 397 Carlantino (founder/genetic isolate) individuals, 790 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,005 Mylopotamos (founder/genetic isolate) individuals, 875 Pomak (founder/genetic isolate) individuals, 1,754 Val Borbera (founder/genetic isolate) individuals 206,723 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 139 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST008161 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Waist circumference 1,254 whole genome sequenced European ancestry individuals, 3,072 whole genome sequenced individuals, 41,450 European ancestry individuals, 397 Carlantino (founder/genetic isolate) individuals, 791 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,060 Mylopotamos (founder/genetic isolate) individuals, 887 Pomak (founder/genetic isolate) individuals, 1,754 Val Borbera (founder/genetic isolate) individuals 206,737 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 118 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST008160 Genome-wide genotyping array 2019-07-17 28552196 Tachmazidou I 2017-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28552196 Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits. Hip circumference 1,254 whole genome sequenced European ancestry individuals, 3,074 whole genome sequenced individuals, 29,716 European ancestry individuals, 400 Carlantino (founder/genetic isolate) individuals, 701 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,050 Mylopotamos (founder/genetic isolate) individuals, 883 Pomak (founder/genetic isolate) individuals 205,909 European ancestry individuals Affymetrix, Illumina, Perlegen [15844966] (imputed) 114 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST008162 Genome-wide genotyping array 2017-11-30 29059683 Michailidou K 2017-10-23 Nature www.ncbi.nlm.nih.gov/pubmed/29059683 Association analysis identifies 65 new breast cancer risk loci. Breast cancer 76,192 European ancestry cases, 63,082 European ancestry controls 46,785 European ancestry cases, 42,892 European ancestry controls, 14,068 East Asian ancestry cases, 13,104 East Asian ancestry controls Illumina [~ 11800000] (imputed) 803 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST004988 Genome-wide genotyping array 2018-04-25 22922229 Cooper JD 2012-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22922229 Seven newly identified loci for autoimmune thyroid disease. Graves' disease 2,285 European ancestry cases, 9,364 European ancestry controls NA Illumina [103875] 12 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST005526 Targeted genotyping array [ImmunoChip] 2018-04-25 22922229 Cooper JD 2012-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22922229 Seven newly identified loci for autoimmune thyroid disease. Hashimoto thyroiditis 462 European ancestry cases, 9,364 European ancestry controls NA Illumina [103875] 1 Hashimoto's thyroiditis http://www.ebi.ac.uk/efo/EFO_0003779 GCST005525 Targeted genotyping array [ImmunoChip] 2018-04-25 22922229 Cooper JD 2012-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22922229 Seven newly identified loci for autoimmune thyroid disease. Autoimmune thyroid diseases (Graves disease or Hashimoto's thyroiditis) 2,282 European ancestry Graves disease cases, 451 European ancestry Hashimoto's thyroiditis cases, 9364 European ancestry controls NA Illumina [103875] 11 autoimmune thyroid disease, Hashimoto's thyroiditis, Graves disease http://www.ebi.ac.uk/efo/EFO_0006812, http://www.ebi.ac.uk/efo/EFO_0003779, http://www.ebi.ac.uk/efo/EFO_0004237 GCST005524 Targeted genotyping array [ImmunoChip] 2017-10-02 28800603 Arpawong TE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800603 Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Verbal memory performance (delayed recall level) 7,486 European ancestry individuals aged 50 years or older NA Illumina [at least 1198956] (imputed) 1 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST004831 Genome-wide genotyping array 2017-10-02 28800603 Arpawong TE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800603 Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Verbal memory performance (residualized delayed recall change) 7,486 European ancestry individuals aged 50 years or older 6,898 European ancestry individuals aged 50 years or older Illumina [at least 1198956] (imputed) 4 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST004830 Genome-wide genotyping array 2017-10-02 28800603 Arpawong TE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800603 Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Verbal memory performance (immediate recall change) 7,486 European ancestry individuals aged 50 years or older 6,898 European ancestry individuals aged 50 years or older Illumina [at least 1198956] (imputed) 4 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST004827 Genome-wide genotyping array 2017-10-02 28800603 Arpawong TE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800603 Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Verbal memory performance (residualized delayed recall level) 7,486 European ancestry individuals aged 50 years or older 6,898 European ancestry individuals aged 50 years or older Illumina [at least 1198956] (imputed) 7 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST004829 Genome-wide genotyping array 2017-10-02 28800603 Arpawong TE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800603 Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Verbal memory performance (immediate recall level) 7,486 European ancestry individuals aged 50 years or older 6,898 European ancestry individuals aged 50 years or older Illumina [at least 1198956] (imputed) 3 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST004828 Genome-wide genotyping array 2017-10-02 28800603 Arpawong TE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800603 Genetic variants specific to aging-related verbal memory: Insights from GWASs in a population-based cohort. Verbal memory performance (delayed recall change) 7,486 European ancestry individuals aged 50 years or older NA Illumina [at least 1198956] (imputed) 0 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST004832 Genome-wide genotyping array 2018-05-30 29203360 Sanders MGH 2017-12-02 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/29203360 The genetics of seborrheic dermatitis: a candidate gene approach and pilot genome-wide association study. Seborrheic dermatitis 609 European and unknown ancestry cases, 3441 European and unknown ancestry controls NA Illumina [9008729] (imputed) 12 seborrheic dermatitis http://www.ebi.ac.uk/efo/EFO_1000764 GCST005655 Genome-wide genotyping array 2018-08-08 24532676 Kim K 2014-02-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/24532676 High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. Rheumatoid arthritis (ACPA-positive) 2,234 Korean ancestry cases, 7,065 Korean ancestry controls, 10,288 European ancestry cases, 35,502 European ancestry controls NA Illumina [133816] (imputed) 52 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST006048 Genome-wide genotyping array, Targeted genotyping array [ImmunoChip] 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. Insulin levels in response to oral glucose tolerance test (fasting) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 1 insulin measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004467, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005159 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. Glucagon levels in response to oral glucose tolerance test (fasting) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 4 glucagon measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008463, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005162 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. GIP levels in response to oral glucose tolerance test (fasting) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 2 glucose-dependent insulinotropic peptide measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008464, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005167 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. GLP-1 levels in response to oral glucose tolerance test (fasting) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 4 glucagon-like peptide-1 measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008465, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005164 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. Insulin levels in response to oral glucose tolerance test (30 minutes) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 3 insulin measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004467, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005160 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. Insulin levels in response to oral glucose tolerance test (120 minutes) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 1 insulin measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004467, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005161 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. GLP-1 levels in response to oral glucose tolerance test (120 minutes) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 1 glucagon-like peptide-1 measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008465, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005165 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. GIP levels in response to oral glucose tolerance test (120 minutes) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 12 glucose-dependent insulinotropic peptide measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008464, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005166 Genome-wide genotyping array 2018-01-17 29093273 Almgren P 2017-11-02 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29093273 Genetic determinants of circulating GIP and GLP-1 concentrations. Glucagon levels in response to oral glucose tolerance test (120 minutes) 3,344 Swedish ancestry individuals 4,905 Finnish ancestry individuals Illumina [at least 81396] 2 glucagon measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008463, http://www.ebi.ac.uk/efo/EFO_0004307 GCST005163 Genome-wide genotyping array 2017-12-05 29097388 Magvanjav O 2017-11-02 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29097388 Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials. Uncontrolled blood pressure in combination therapy (beta blocker and thiazide diuretic) 123 European ancestry cases, 191 European ancestry controls 85 European ancestry cases, 136 European ancestry controls, 81 Hispanic cases, 112 Hispanic controls Illumina [NR] (imputed) 2 blood pressure, response to thiazide, response to beta blocker http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0007981, http://www.ebi.ac.uk/efo/EFO_0007766 GCST005039 Genome-wide genotyping array 2017-12-05 29097388 Magvanjav O 2017-11-02 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29097388 Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials. Systolic blood pressure in combination therapy (beta blocker and thiazide diuretic) 314 European ancestry individuals 221 European ancestry individuals, 193 Hispanic individuals Illumina [NR] (imputed) 1 systolic blood pressure, response to thiazide, response to beta blocker http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0007981, http://www.ebi.ac.uk/efo/EFO_0007766 GCST005040 Genome-wide genotyping array 2017-12-05 29097388 Magvanjav O 2017-11-02 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29097388 Genetic Variants Associated With Uncontrolled Blood Pressure on Thiazide Diuretic/β-Blocker Combination Therapy in the PEAR (Pharmacogenomic Evaluation of Antihypertensive Responses) and INVEST (International Verapamil-SR Trandolapril Study) Trials. Diastolic blood pressure in combination therapy (beta blocker and thiazide diuretic) 314 European ancestry individuals 221 European ancestry individuals, 193 Hispanic individuals Illumina [NR] (imputed) 3 diastolic blood pressure, response to thiazide, response to beta blocker http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0007981, http://www.ebi.ac.uk/efo/EFO_0007766 GCST005041 Genome-wide genotyping array 2017-12-05 29064472 Lencer R 2017-10-24 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29064472 Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. Pursuit maintenance gain in psychotic disorders 114 African ancestry schizophrenia cases, 69 African schizo-affective cases, 41 African ancestry bipolar disorder cases, 116 European ancestry schizophrenia cases, 86 European ancestry schizo-affective cases, 165 European ancestry bipolar disorder cases NA Illumina [4404269] (imputed) 11 pursuit maintenance gain measurement http://www.ebi.ac.uk/efo/EFO_0008433 GCST005028 Genome-wide genotyping array 2017-12-05 29064472 Lencer R 2017-10-24 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29064472 Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. Initial pursuit acceleration 114 African ancestry schizophrenia cases, 69 African schizo-affective cases, 41 African ancestry bipolar disorder cases, 76 African ancestry controls, 116 European ancestry schizophrenia cases, 86 European ancestry schizo-affective cases, 165 European ancestry bipolar disorder cases, 182 European ancestry controls NA Illumina [4404269] (imputed) 56 initial pursuit acceleration http://www.ebi.ac.uk/efo/EFO_0008434 GCST005023 Genome-wide genotyping array 2017-12-05 29064472 Lencer R 2017-10-24 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29064472 Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. Pursuit maintenance gain 114 African ancestry schizophrenia cases, 69 African schizo-affective cases, 41 African ancestry bipolar disorder cases, 76 African ancestry controls, 116 European ancestry schizophrenia cases, 86 European ancestry schizo-affective cases, 165 European ancestry bipolar disorder cases, 182 European ancestry controls NA Illumina [4404269] (imputed) 111 pursuit maintenance gain measurement http://www.ebi.ac.uk/efo/EFO_0008433 GCST005024 Genome-wide genotyping array 2017-12-05 29064472 Lencer R 2017-10-24 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29064472 Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. Anti-saccade response 114 African ancestry schizophrenia cases, 69 African schizo-affective cases, 41 African ancestry bipolar disorder cases, 76 African ancestry controls, 116 European ancestry schizophrenia cases, 86 European ancestry schizo-affective cases, 165 European ancestry bipolar disorder cases, 182 European ancestry controls NA Illumina [4404269] (imputed) 41 antisaccade response measurement http://www.ebi.ac.uk/efo/EFO_0006874 GCST005025 Genome-wide genotyping array 2017-12-05 29064472 Lencer R 2017-10-24 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29064472 Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. Initial pursuit acceleration in psychotic disorders 114 African ancestry schizophrenia cases, 69 African schizo-affective cases, 41 African ancestry bipolar disorder cases, 116 European ancestry schizophrenia cases, 86 European ancestry schizo-affective cases, 165 European ancestry bipolar disorder cases. NA Illumina [4404269] (imputed) 22 initial pursuit acceleration http://www.ebi.ac.uk/efo/EFO_0008434 GCST005026 Genome-wide genotyping array 2017-12-05 29064472 Lencer R 2017-10-24 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29064472 Genome-wide association studies of smooth pursuit and antisaccade eye movements in psychotic disorders: findings from the B-SNIP study. Anti-saccade error rate in psychotic disorders 114 African ancestry schizophrenia cases, 69 African schizo-affective cases, 41 African ancestry bipolar disorder cases, 116 European ancestry schizophrenia cases, 86 European ancestry schizo-affective cases, 165 European ancestry bipolar disorder cases NA Illumina [4404269] (imputed) 3 antisaccade response measurement http://www.ebi.ac.uk/efo/EFO_0006874 GCST005027 Genome-wide genotyping array 2017-06-01 28062682 Carr DF 2017-01-05 J Antimicrob Chemother www.ncbi.nlm.nih.gov/pubmed/28062682 Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population. Nevirapine-induced hypersensitivity in HIV (drug-induced liver injury) 21 Sub-saharan African ancestry cases, 182 Sub-saharan African ancestry controls 16 Sub-Saharan African ancestry cases, 27 African ancestry cases, 60 Sub-Saharan African ancestry controls, 8 African ancestry controls Illumina [14218511] (imputed) 1 response to reverse transcriptase inhibitor, drug-induced liver injury http://purl.obolibrary.org/obo/GO_0061479, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004114 Genome-wide genotyping array 2017-06-01 28062682 Carr DF 2017-01-05 J Antimicrob Chemother www.ncbi.nlm.nih.gov/pubmed/28062682 Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population. Nevirapine-induced hypersensitivity in HIV (Stevens-Johnson syndrome or toxic epidermal necrosis) 51 Sub-saharan African ancestry cases, 182 Sub-saharan African ancestry controls 11 Sub-Saharan African ancestry cases, 27 African ancestry cases, 60 Sub-Saharan African ancestry controls, 8 African ancestry controls Illumina [14218511] (imputed) 1 response to reverse transcriptase inhibitor, Stevens-Johnson syndrome, toxic epidermal necrolysis http://purl.obolibrary.org/obo/GO_0061479, http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775 GCST004115 Genome-wide genotyping array 2017-06-01 28062682 Carr DF 2017-01-05 J Antimicrob Chemother www.ncbi.nlm.nih.gov/pubmed/28062682 Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population. Nevirapine-induced hypersensitivity in HIV (hypersensitivity syndrome) 23 Sub-saharan African ancestry cases, 182 Sub-saharan African ancestry controls NA Illumina [14218511] (imputed) 0 response to reverse transcriptase inhibitor, drug hypersensitivity syndrome http://purl.obolibrary.org/obo/GO_0061479, http://www.ebi.ac.uk/efo/EFO_1002004 GCST004116 Genome-wide genotyping array 2017-06-01 28062682 Carr DF 2017-01-05 J Antimicrob Chemother www.ncbi.nlm.nih.gov/pubmed/28062682 Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population. Nevirapine-induced hypersensitivity in HIV (rash) 56 Sub-saharan African ancestry cases, 182 Sub-saharan African ancestry controls 27 Sub-Saharan African ancestry cases, 60 Sub-Saharan African ancestry controls Illumina [14218511] (imputed) 0 response to reverse transcriptase inhibitor, maculopapular eruption http://purl.obolibrary.org/obo/GO_0061479, http://www.ebi.ac.uk/efo/EFO_1001253 GCST004117 Genome-wide genotyping array 2017-06-01 28062682 Carr DF 2017-01-05 J Antimicrob Chemother www.ncbi.nlm.nih.gov/pubmed/28062682 Genome-wide association study of nevirapine hypersensitivity in a sub-Saharan African HIV-infected population. Nevirapine-induced hypersensitivity in HIV 151 Sub-saharan African ancestry cases, 182 Sub-saharan African ancestry controls 62 Sub-Saharan African ancestry cases, 60 Sub-Saharan African ancestry controls Illumina [14218511] (imputed) 1 response to reverse transcriptase inhibitor, hypersensitivity reaction disease http://purl.obolibrary.org/obo/GO_0061479, http://www.ebi.ac.uk/efo/EFO_1002003 GCST004118 Genome-wide genotyping array 2017-08-10 28641921 Li J 2017-05-15 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/28641921 Genome-wide association and interaction studies of CSF T-tau/Aβ42 ratio in ADNI cohort. Cerebrospinal fluid t-tau levels 113 European ancestry Alzheimer's disease cases, 207 European ancestry individuals with late mild cognitive impairment, 239 European ancestry individuals with early mild cognitive impairment, 85 European ancestry individuals with significant memory concern, 199 European ancestry controls. NA Illumina [563980] 7 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST004491 Genome-wide genotyping array 2017-08-10 28641921 Li J 2017-05-15 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/28641921 Genome-wide association and interaction studies of CSF T-tau/Aβ42 ratio in ADNI cohort. Cerebrospinal fluid AB1-42 levels 113 European ancestry Alzheimer's disease cases, 207 European ancestry individuals with late mild cognitive impairment, 239 European ancestry individuals with early mild cognitive impairment, 85 European ancestry individuals with significant memory concern, 199 European ancestry controls. NA Illumina [563980] 4 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST004492 Genome-wide genotyping array 2017-08-10 28641921 Li J 2017-05-15 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/28641921 Genome-wide association and interaction studies of CSF T-tau/Aβ42 ratio in ADNI cohort. Cerebrospinal fluid t-tau:AB1-42 ratio 113 European ancestry Alzheimer's disease cases, 207 European ancestry individuals with late mild cognitive impairment, 239 European ancestry individuals with early mild cognitive impairment, 85 European ancestry individuals with significant memory concern, 199 European ancestry controls. NA Illumina [563980] 24 t-tau:beta-amyloid 1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0007708 GCST004490 Genome-wide genotyping array 2017-11-13 19330027 Ahmed S 2009-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19330027 Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Breast cancer 390 European ancestry cases, 364 European ancestry controls 38,430 European ancestry cases, 2,572 East Asian ancestry cases, 41,926 European ancestry controls, 2,059 East Asian ancestry controls Illumina, Perlegen [up to 206586] 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST004948 Genome-wide genotyping array 2017-11-13 19330027 Ahmed S 2009-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19330027 Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2. Breast cancer 390 European ancestry cases, 364 European ancestry controls 11,645 European ancestry cases, 12,015 European ancestry controls Perlegen [up to 206586] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST004949 Genome-wide genotyping array 2018-08-17 29107063 Yashin AI 2017-10-26 Exp Gerontol www.ncbi.nlm.nih.gov/pubmed/29107063 Hidden heterogeneity in Alzheimer's disease: Insights from genetic association studies and other analyses. Alzheimer's disease at least 3,569 European, Black, and unknown ancestry cases, at least 19,085 European, Black, and unknown ancestry controls NA Illumina [up to 1329158] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST006121 Genome-wide genotyping array 2018-08-17 29107063 Yashin AI 2017-10-26 Exp Gerontol www.ncbi.nlm.nih.gov/pubmed/29107063 Hidden heterogeneity in Alzheimer's disease: Insights from genetic association studies and other analyses. Alzheimer's disease (age of onset) 12,169 European ancestry individuals, 2,078 Black individuals, 4,053 unknown ancestry individuals NA Illumina [up to 1329158] 1 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST006120 Genome-wide genotyping array 2017-05-15 28046027 Kim T 2017-01-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/28046027 Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup. NHDL cholesterol to HDL cholesterol ratio 5,292 Korean ancestry individuals 2,567 Korean ancestry individuals Affymetrix [310746] 1 non-HDL cholesterol:HDL cholesterol ratio http://www.ebi.ac.uk/efo/EFO_0007931 GCST004035 Genome-wide genotyping array 2017-05-15 28046027 Kim T 2017-01-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/28046027 Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup. LDL cholesterol to HDL cholesterol ratio 5,292 Korean ancestry individuals 2,567 Korean ancestry individuals Affymetrix [310746] 2 LDL cholesterol:HDL cholesterol ratio http://www.ebi.ac.uk/efo/EFO_0007930 GCST004036 Genome-wide genotyping array 2017-05-15 28046027 Kim T 2017-01-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/28046027 Genome-Wide Association Study Reveals Four Loci for Lipid Ratios in the Korean Population and the Constitutional Subgroup. Triglyceride to HDL cholesterol ratio 5,292 Korean ancestry individuals 2,567 Korean ancestry individuals Affymetrix [310746] 2 triglyceride:HDL cholesterol ratio http://www.ebi.ac.uk/efo/EFO_0007929 GCST004037 Genome-wide genotyping array 2017-12-20 29127183 Seyerle AA 2017-11-10 Heart www.ncbi.nlm.nih.gov/pubmed/29127183 Genome-wide association study of PR interval in Hispanics/Latinos identifies novel locus at ID2. PR interval 14,756 Hispanic individuals 4,296 European ancestry individuals, 3,763 African American individuals, 6,805 East Asian ancestry individuals Affymetrix, Illumina [18828993] (imputed) 9 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST005080 Genome-wide genotyping array 2017-10-09 28813576 Persad PJ 2017-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/28813576 Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Advanced age-related macular degeneration Up to 16,144 European ancestry cases, up to 17,832 European ancestry controls NA Illumina [3866946] (imputed) 2 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST004868 Genome-wide genotyping array 2017-10-09 28813576 Persad PJ 2017-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/28813576 Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Age-related macular degeneration (SNP x mitochondrial T5004C interaction) 15,407 European ancestry cases, 16,350 European ancestry controls NA Illumina [3866946] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST004869 Genome-wide genotyping array 2017-10-09 28813576 Persad PJ 2017-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/28813576 Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Age-related macular degeneration (SNP x mitochondrial A4917G interaction) 16,122 European ancestry cases, 17,810 European ancestry controls NA Illumina [3866946] (imputed) 1 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST004870 Genome-wide genotyping array 2017-10-09 28813576 Persad PJ 2017-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/28813576 Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Age-related macular degeneration (SNP x mitochondrial G12771A interaction) 15,413 European ancestry cases, 16,351 European ancestry controls NA Illumina [3866946] (imputed) 1 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST004871 Genome-wide genotyping array 2017-10-09 28813576 Persad PJ 2017-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/28813576 Joint Analysis of Nuclear and Mitochondrial Variants in Age-Related Macular Degeneration Identifies Novel Loci TRPM1 and ABHD2/RLBP1. Age-related macular degeneration (SNP x mitochondrial C16069T interaction) 16,042 European ancestry cases, 17,734 European ancestry controls NA Illumina [3866946] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST004872 Genome-wide genotyping array 2017-09-12 28701861 Randall CL 2017-06-15 Pain Res Manag www.ncbi.nlm.nih.gov/pubmed/28701861 A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain. Fear of severe pain Up to 1,367 European ancestry individuals, up to 159 African American individuals, up to 13 Hispanic individuals, up to 23 Asian, Native American and other ancestry individuals, up to 21 individuals NA Illumina [8591557] (imputed) 8 fear of severe pain measurement http://www.ebi.ac.uk/efo/EFO_0008338 GCST004709 Genome-wide genotyping array 2017-09-12 28701861 Randall CL 2017-06-15 Pain Res Manag www.ncbi.nlm.nih.gov/pubmed/28701861 A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain. Fear of minor pain Up to 1,367 European ancestry individuals, up to 159 African American individuals, up to 13 Hispanic individuals, up to 23 Asian, Native American and other ancestry individuals, up to 21 individuals NA Illumina [8591557] (imputed) 19 fear of minor pain measurement http://www.ebi.ac.uk/efo/EFO_0008340 GCST004708 Genome-wide genotyping array 2017-09-12 28701861 Randall CL 2017-06-15 Pain Res Manag www.ncbi.nlm.nih.gov/pubmed/28701861 A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain. Fear of medical pain (dental) Up to 1,367 European ancestry individuals, up to 159 African American individuals, up to 13 Hispanic individuals, up to 23 Asian, Native American and other ancestry individuals, up to 21 individuals NA Illumina [8591557] (imputed) 6 fear of medical pain measurement http://www.ebi.ac.uk/efo/EFO_0008339 GCST004707 Genome-wide genotyping array 2017-09-12 28701861 Randall CL 2017-06-15 Pain Res Manag www.ncbi.nlm.nih.gov/pubmed/28701861 A Preliminary Genome-Wide Association Study of Pain-Related Fear: Implications for Orofacial Pain. Fear of pain Up to 1,367 European ancestry individuals, up to 159 African American individuals, up to 13 Hispanic individuals, up to 23 Asian, Native American and other ancestry individuals, up to 21 individuals NA Illumina [8591557] (imputed) 4 fear of pain measurement http://www.ebi.ac.uk/efo/EFO_0008330 GCST004706 Genome-wide genotyping array 2017-11-20 28927378 Qian DC 2017-09-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/28927378 Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. Caudate activity during disappointment 106 individuals NA Illumina [at least 621854] (imputed) 0 caudate nucleus measurement, response to disappointment, functional brain measurement http://www.ebi.ac.uk/efo/EFO_0008387, http://www.ebi.ac.uk/efo/EFO_0008397, http://www.ebi.ac.uk/efo/EFO_0007849 GCST004969 Genome-wide genotyping array 2017-11-20 28927378 Qian DC 2017-09-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/28927378 Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. Caudate activity during reward 106 individuals NA Illumina [at least 621854] (imputed) 31 caudate nucleus measurement, functional brain measurement, response to reward http://www.ebi.ac.uk/efo/EFO_0008387, http://www.ebi.ac.uk/efo/EFO_0007849, http://www.ebi.ac.uk/efo/EFO_0008396 GCST004970 Genome-wide genotyping array 2017-11-20 28927378 Qian DC 2017-09-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/28927378 Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. Putamen activity during reward 106 individuals NA Illumina [at least 621854] (imputed) 0 functional brain measurement, putamen measurement, response to reward http://www.ebi.ac.uk/efo/EFO_0007849, http://www.ebi.ac.uk/efo/EFO_0008389, http://www.ebi.ac.uk/efo/EFO_0008396 GCST004971 Genome-wide genotyping array 2017-11-20 28927378 Qian DC 2017-09-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/28927378 Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. Putamen actvity during disappointment 106 individuals NA Illumina [at least 621854] (imputed) 0 response to disappointment, functional brain measurement, putamen measurement http://www.ebi.ac.uk/efo/EFO_0008397, http://www.ebi.ac.uk/efo/EFO_0007849, http://www.ebi.ac.uk/efo/EFO_0008389 GCST004972 Genome-wide genotyping array 2018-07-19 29059373 Li Y 2017-10-20 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/29059373 Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Smoking interaction in non-small cell lung cancer (1df test) 1,399 European ancestry never smoker cases, 11,937 European ancestry smoker cases NA Illumina [502933] 0 smoking behavior, non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0003060 GCST005910 Genome-wide genotyping array 2018-07-19 29059373 Li Y 2017-10-20 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/29059373 Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Smoking interaction in lung adenocarcinoma (1df test) 1,097 European ancestry never smoker cases, 5,918 European ancestry smoker cases NA Illumina [502933] 0 smoking behavior, lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0000571 GCST005909 Genome-wide genotyping array 2018-07-19 29059373 Li Y 2017-10-20 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/29059373 Genome-wide interaction study of smoking behavior and non-small cell lung cancer risk in Caucasian population. Smoking interaction in squamous cell lung cancer (1df test) 159 European ancestry never smoker cases, 4,370 European ancestry smoker cases NA Illumina [502933] 0 smoking behavior, squamous cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0000708 GCST005911 Genome-wide genotyping array 2018-01-12 29093028 Corre T 2017-11-01 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29093028 Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes. Urinary magnesium-to-creatinine ratio up to 5,810 European ancestry individuals, up to 1,541 Val Borbera (founder/genetic isolate) individuals, up to 281 Carlantino (founder/genetic isolate) individuals, up to 889 Korcula (founder/genetic isolate) individuals, up to 489 Split (founder/genetic isolate) individuals, up to 195 Vis (founder/genetic isolate) individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 2 magnesium:creatinine ratio measurement http://www.ebi.ac.uk/efo/EFO_0008449 GCST005124 Genome-wide genotyping array 2018-01-12 29093028 Corre T 2017-11-01 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29093028 Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes. Fractional excretion of magnesium 5,265 European ancestry individuals, 1,541 Val Borbera (founder/genetic isolate) individuals, 281 Carlantino (founder/genetic isolate) individuals, 889 Korcula (founder/genetic isolate) individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 0 fractional excretion of magnesium measurement http://www.ebi.ac.uk/efo/EFO_0008450 GCST005126 Genome-wide genotyping array 2018-01-12 29093028 Corre T 2017-11-01 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29093028 Genome-Wide Meta-Analysis Unravels Interactions between Magnesium Homeostasis and Metabolic Phenotypes. Serum magnesium levels 5,265 European ancestry individuals, 1,541 Val Borbera (founder/genetic isolate) individuals, 281 Carlantino (founder/genetic isolate) individuals, 889 Korcula (founder/genetic isolate) individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 1 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST005125 Genome-wide genotyping array 2017-12-18 29123153 Lee TH 2017-11-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29123153 A genome-wide association study links small-vessel ischemic stroke to autophagy. Small vessel stroke 342 Chinese ancestry cases, 1,731 Chinese ancestry control 188 Chinese ancestry cases, 1,265 Chinese ancestry control Affymetrix [552090] (imputed) 7 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST005057 Genome-wide genotyping array 2017-12-14 29118346 Sakamoto Y 2017-11-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29118346 Genome-wide Association Study of Idiopathic Osteonecrosis of the Femoral Head. Idiopathic osteonecrosis of the femoral head 1,547 Japanese ancestry cases, 59,103 Japanese ancestry controls NA Illumina [525208] 2 idiopathic osteonecrosis of the femoral head http://www.ebi.ac.uk/efo/EFO_1001930 GCST005048 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Food allergy (parent-of-origin effect) 482 European ancestry trios, 19 European ancestry father-child pairs, 59 European ancestry mother-child pairs, 28 European ancestry affected children NA Illumina [NR] 6 food allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007016, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005721 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Peanut allergy (parent-of-origin effect) 247 European ancestry trios, 7 European ancestry father-child pairs, 33 European ancestry mother-child pairs, 14 European ancestry affected child NA Illumina [NR] 5 peanut allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007017, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005727 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Milk allergy (parent-of-origin effect) 230 European ancestry trios, 10 European ancestry father-child pairs, 25 European ancestry mother-child pairs, 10 European ancestry affected child NA Illumina [NR] 2 milk allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007019, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005726 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Egg allergy (parent-of-origin effect) 169 European ancestry trios, 5 European ancestry father-child pairs, 19 European ancestry mother-child pairs, 8 European ancestry affected child NA Illumina [NR] 3 egg allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007018, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005725 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Food allergy (maternal genetic effects) 588 European ancestry complete and incomplete trios NA Illumina [NR] 5 food allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007016, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005724 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Peanut allergy (maternal genetic effects) 301 European ancestry complete and incomplete trios NA Illumina [NR] 4 peanut allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007017, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005723 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Milk allergy (maternal genetic effects) 275 European ancestry complete and incomplete trios NA Illumina [NR] 2 milk allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007019, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005722 Genome-wide genotyping array 2018-06-22 29489655 Liu X 2018-03-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29489655 Genome-wide association study of maternal genetic effects and parent-of-origin effects on food allergy. Egg allergy (maternal genetic effects) 201 European ancestry complete and incomplete trios NA Illumina [NR] 5 egg allergy measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007018, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005728 Genome-wide genotyping array 2018-01-09 26545403 Bei JX 2016-01-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/26545403 A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry. Nasopharyngeal carcinoma 2,152 Chinese ancestry cases, 3,740 Chinese ancestry controls 4,716 Chinese ancestry cases, 5,379 Chinese ancestry controls Illumina [Sequenom custom array used in replication] (imputed) 8 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST005113 Genome-wide genotyping array 2018-04-25 23603761 Hinks A 2013-04-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23603761 Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. Juvenile idiopathic arthritis (oligoarticular or rheumatoid factor-negative polyarticular) 2,816 European ancestry cases, 13,056 European ancestry controls NA Illumina [123003] 31 systemic juvenile idiopathic arthritis, polyarticular juvenile idiopathic arthritis, rheumatoid factor negative, oligoarticular juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_1001999, http://www.ebi.ac.uk/efo/EFO_1002020, http://www.ebi.ac.uk/efo/EFO_1002019 GCST005528 Targeted genotyping array [ImmunoChip] 2018-04-17 29458411 Chung J 2018-02-20 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/29458411 Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease. Neuritic plaques or neurofibrillary tangles or cerebral amyloid angiopathy (pleiotropy) 3,135 European ancestry Alzheimer's disease cases, 463 European ancestry controls NA NR [6500000] (imputed) 3 neuritic plaque measurement, cerebral amyloid angiopathy, neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006798, http://www.ebi.ac.uk/efo/EFO_0006790, http://www.ebi.ac.uk/efo/EFO_0006797 GCST005514 Genome-wide genotyping array 2018-04-17 29458411 Chung J 2018-02-20 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/29458411 Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease. Neuritic plaques or neurofibrillary tangles (pleiotropy) 3,135 European ancestry Alzheimer's disease cases, 463 European ancestry controls NA NR [6500000] (imputed) 4 neuritic plaque measurement, neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006798, http://www.ebi.ac.uk/efo/EFO_0006797 GCST005516 Genome-wide genotyping array 2018-04-17 29458411 Chung J 2018-02-20 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/29458411 Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease. Neuritic plaques or cerebral amyloid angiopathy (pleiotropy) 3,135 European ancestry Alzheimer's disease cases, 463 European ancestry controls NA NR [6500000] (imputed) 3 neuritic plaque measurement, cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0006798, http://www.ebi.ac.uk/efo/EFO_0006790 GCST005515 Genome-wide genotyping array 2018-04-17 29458411 Chung J 2018-02-20 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/29458411 Genome-wide pleiotropy analysis of neuropathological traits related to Alzheimer's disease. Neurofibrillary tangles or cerebral amyloid angiopathy (pleiotropy) 3,135 European ancestry Alzheimer's diseases cases, 463 European ancestry controls NA NR [6500000] (imputed) 2 cerebral amyloid angiopathy, neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006790, http://www.ebi.ac.uk/efo/EFO_0006797 GCST005517 Genome-wide genotyping array 2017-12-05 29104669 Chen L 2017-11-01 Exp Ther Med www.ncbi.nlm.nih.gov/pubmed/29104669 Genome-wide association study for SNPs associated with PCOS in human patients. Polycystic ovary syndrome 200 Chinese ancestry cases, 228 Chinese ancestry controls 200 Chinese ancestry cases, 1,400 Chinese ancestry controls NR [~ 900000] 0 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST005043 Genome-wide genotyping array 2017-06-21 28358029 Afshari NA 2017-03-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28358029 Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy. Fuchs's corneal dystrophy 1,404 European ancestry cases, 2,564 European ancestry controls 671 European ancestry cases, 778 European ancestry controls Illumina [8680745] (imputed) 6 Fuchs endothelial corneal dystrophy http://www.orpha.net/ORDO/Orphanet_98974 GCST004217 Genome-wide genotyping array 2017-06-23 28355232 Ward-Caviness CK 2017-03-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/28355232 A genome-wide trans-ethnic interaction study links the PIGR-FCAMR locus to coronary atherosclerosis via interactions between genetic variants and residential exposure to traffic. Coronary atherosclerosis (increased number of diseased vessels) (traffic exposure interaction) 1,562 European ancestry individuals, 538 African American individuals NA Illumina [at least 756588] 15 coronary atherosclerosis measurement, traffic air pollution measurement http://www.ebi.ac.uk/efo/EFO_0007938, http://www.ebi.ac.uk/efo/EFO_0007908 GCST004224 Genome-wide genotyping array 2017-12-07 29097723 Darlow JM 2017-11-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29097723 Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. Primary vesicoureteric reflux 1156 European ancestry cases and at least 1156 European ancestry controls from 548 families NA Affymetrix [3563212] (imputed) 1 vesicoureteral reflux http://www.ebi.ac.uk/efo/EFO_0007536 GCST005044 Genome-wide genotyping array 2017-12-07 29097723 Darlow JM 2017-11-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29097723 Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux. Primary vesicoureteric reflux 1147 European ancestry cases, 3789 European ancestry controls NA Affymetrix [119548] 0 vesicoureteral reflux http://www.ebi.ac.uk/efo/EFO_0007536 GCST005045 Genome-wide genotyping array 2017-12-18 29077507 Chen H 2017-10-27 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/29077507 Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men. Obstructive sleep apnea trait (apnea hypopnea index) 677 African American women, 544 African American men, 115 Asian women, 113 Asian men, 1,825 European ancestry women, 3,902 European ancestry men, 7,492 Hispanic women, 5,065 Hispanic men NA Affymetrix, Illumina [NR] (imputed) 31 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST005051 Genome-wide genotyping array 2017-12-18 29077507 Chen H 2017-10-27 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/29077507 Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men. Obstructive sleep apnea during non-REM sleep (apnea hypopnea index) 1,221 African American individuals, 228 Asian individuals, 5,727 European ancestry individuals,12,557 Hispanic individuals 206 African American individuals, 2,792 Asian individuals, 5,315 European ancestry individuals, 55 European ancestry obstructive sleep apnea cases, 12 European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 sleep apnea measurement during non-REM sleep http://www.ebi.ac.uk/efo/EFO_0008456 GCST005049 Genome-wide genotyping array 2017-12-18 29077507 Chen H 2017-10-27 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/29077507 Multi-ethnic Meta-analysis Identifies RAI1 as a Possible Obstructive Sleep Apnea Related Quantitative Trait Locus in Men. Obstructive sleep apnea during REM sleep (apnea hypopnea index) 677 African American women, 544 African American men, 115 Asian women, 113 Asian men, 1,825 European ancestry women, 3,902 European ancestry men, 7,492 Hispanic women, 5,065 Hispanic men NA Affymetrix, Illumina [NR] (imputed) 7 sleep apnea measurement during REM sleep http://www.ebi.ac.uk/efo/EFO_0008455 GCST005050 Genome-wide genotyping array 2018-05-14 22961000 Liu JZ 2012-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22961000 Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. Primary biliary cirrhosis 2,861 British and Irish ancestry cases, 8,514 British and Irish ancestry controls NA Illumina [237619] (imputed) 47 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST005581 Targeted genotyping array [ImmunoChip] 2018-12-18 29360470 Miron J 2018-01-19 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29360470 CDK5RAP2 gene and tau pathophysiology in late-onset sporadic Alzheimer's disease. Late-onset Alzheimer's disease 966 Quebec (founder/genetic isolate) ancestry cases, 977 Quebec (founder/genetic isolate) controls 340 cases, 195 controls Illumina [NR] 1 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST006806 Genome-wide genotyping array 2017-06-29 28360221 Boger CA 2017-03-30 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/28360221 NFAT5 and SLC4A10 Loci Associate with Plasma Osmolality. Blood osmolality (transformed sodium) 45,889 European ancestry individuals, up to 8,765 Asian Indian ancestry individuals, up to 7,215 African ancestry individuals 17,637 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 37 blood osmolality measurement http://www.ebi.ac.uk/efo/EFO_0007967 GCST004267 Genome-wide genotyping array 2018-01-12 29095316 Suh Y 2017-11-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29095316 Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function. Lung function (maximal voluntary ventilation) 8,842 Korean ancestry individuals NA Affymetrix [2476376] (imputed) 3 maximal voluntary ventilation, pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0008431, http://www.ebi.ac.uk/efo/EFO_0003892 GCST005127 Genome-wide genotyping array 2018-01-12 29095316 Suh Y 2017-11-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29095316 Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function. Lung function (forced expiratory volume in 1 second) 8,842 Korean ancestry individuals NA Affymetrix [2476376] (imputed) 2 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST005132 Genome-wide genotyping array 2018-01-12 29095316 Suh Y 2017-11-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29095316 Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function. Lung function (forced expiratory flow during mid-portion (25% and 75%) of forced vital capacity) 8,842 Korean ancestry individuals NA Affymetrix [2476376] (imputed) 0 maximal midexpiratory flow rate http://www.ebi.ac.uk/efo/EFO_0004313 GCST005129 Genome-wide genotyping array 2018-01-12 29095316 Suh Y 2017-11-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29095316 Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function. Lung function (forced vital capacity) 8,842 Korean ancestry individuals NA Affymetrix [2476376] (imputed) 2 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST005131 Genome-wide genotyping array 2018-01-12 29095316 Suh Y 2017-11-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/29095316 Genome-wide association study for genetic variants related with maximal voluntary ventilation reveals two novel genomic signals associated with lung function. Lung function (FEV1/FVC) 8,842 Korean ancestry individuals NA Affymetrix [2476376] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST005130 Genome-wide genotyping array 2017-11-10 29088834 Kimura M 2017-08-24 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29088834 A genome-wide association analysis identifies PDE1A|DNAJC10 locus on chromosome 2 associated with idiopathic pulmonary arterial hypertension in a Japanese population. Pulmonary arterial hypertension 23 Japanese ancestry cases, 2,002 Japanese ancestry controls 21 Japanese ancestry cases, 991 Japanese ancestry controls Illumina [1347690] 1 pulmonary arterial hypertension http://www.ebi.ac.uk/efo/EFO_0001361 GCST004947 Genome-wide genotyping array 2017-10-20 28935272 Moore KN 2017-09-18 Gynecol Oncol www.ncbi.nlm.nih.gov/pubmed/28935272 Genome-wide association study evaluating single-nucleotide polymorphisms and outcomes in patients with advanced stage serous ovarian or primary peritoneal cancer: An NRG Oncology/Gynecologic Oncology Group study. Progression free survival in serous epithelial ovarian cancer treated with carboplatin and paclitaxel 147 European ancestry women NA Illumina [636555] 4 progression free survival, methylcobalamin deficiency type cblE, ovarian carcinoma, response to cisplatin http://www.ebi.ac.uk/efo/EFO_0004920, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0001075, http://purl.obolibrary.org/obo/GO_0072718 GCST004897 Genome-wide genotyping array 2017-10-20 28935272 Moore KN 2017-09-18 Gynecol Oncol www.ncbi.nlm.nih.gov/pubmed/28935272 Genome-wide association study evaluating single-nucleotide polymorphisms and outcomes in patients with advanced stage serous ovarian or primary peritoneal cancer: An NRG Oncology/Gynecologic Oncology Group study. Overall survival in serous epithelial ovarian cancer treated with paclitaxel and cisplatin 289 European ancestry women NA Illumina [636555] 10 methylcobalamin deficiency type cblE, overall survival, ovarian carcinoma, response to cisplatin http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0001075, http://purl.obolibrary.org/obo/GO_0072718 GCST004896 Genome-wide genotyping array 2018-03-12 29381699 Ravenhall M 2018-01-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29381699 Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania. Severe malaria (adjusted for sickle cell variant rs334) 449 Tanzanian ancestry cases, 465 Tanzanian ancestry controls NA Illumina [15200000] (imputed) 14 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST005357 Genome-wide genotyping array 2018-03-12 29381699 Ravenhall M 2018-01-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29381699 Novel genetic polymorphisms associated with severe malaria and under selective pressure in North-eastern Tanzania. Severe malaria 449 Tanzanian ancestry cases, 465 Tanzanian ancestry controls NA Illumina [15200000] (imputed) 15 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST005356 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Diastolic blood pressure x sodium interaction (1df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 1 sodium measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006336 GCST006112 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Systolic blood pressure x sodium interaction (2df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 2 sodium measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006335 GCST006113 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Diastolic blood pressure x sodium interaction (2df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 2 sodium measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006336 GCST006111 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Mean arterial pressure x sodium interaction (2df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 1 sodium measurement, mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006340 GCST006114 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Systolic blood pressure x sodium interaction (1df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 0 sodium measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006335 GCST006115 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Mean arterial pressure x sodium interaction (1df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 0 sodium measurement, mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006340 GCST006116 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Pulse pressure x sodium interaction (1df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 0 pulse pressure measurement, sodium measurement http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009282 GCST006117 Genome-wide genotyping array 2018-08-16 27271309 Li C 2016-08-01 Hypertension www.ncbi.nlm.nih.gov/pubmed/27271309 Genome-Wide Gene-Sodium Interaction Analyses on Blood Pressure: The Genetic Epidemiology Network of Salt-Sensitivity Study. Pulse pressure x sodium interaction (2df test) 1,876 Han Chinese ancestry individuals 775 Chinese ancestry individuals Affymetrix [2216774] (imputed) 0 pulse pressure measurement, sodium measurement http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009282 GCST006118 Genome-wide genotyping array 2017-12-01 28924203 Ren HY 2017-09-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28924203 The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. White matter microstructure in first episode schizophrenia (right posterior cingulate cortex) 93 Han Chinese cases, 134 Han Chinese controls NA Illumina [6055918] (imputed) 1 white matter microstructure measurement, cingulate cortex measurement http://www.ebi.ac.uk/efo/EFO_0005674, http://www.ebi.ac.uk/efo/EFO_0007738 GCST004992 Genome-wide genotyping array 2017-12-01 28924203 Ren HY 2017-09-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28924203 The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. Total mean fractional anisotropy measurement in first episode schizophrenia 93 Han Chinese cases, 134 Han Chinese controls NA Illumina [6055918] (imputed) 1 mean fractional anisotropy measurement, white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0008399, http://www.ebi.ac.uk/efo/EFO_0005674 GCST004996 Genome-wide genotyping array 2017-12-01 28924203 Ren HY 2017-09-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28924203 The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. White matter microstructure in first episode schizophrenia (left posterior cingulate cortex) 93 Han Chinese cases, 134 Han Chinese controls NA Illumina [6055918] (imputed) 1 white matter microstructure measurement, cingulate cortex measurement http://www.ebi.ac.uk/efo/EFO_0005674, http://www.ebi.ac.uk/efo/EFO_0007738 GCST004995 Genome-wide genotyping array 2017-12-01 28924203 Ren HY 2017-09-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28924203 The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. White matter microstructure in first episode schizophrenia (left inferior parietal cortex) 93 Han Chinese cases, 134 Han Chinese controls NA Illumina [6055918] (imputed) 1 parietal cortex measurement, white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0008420, http://www.ebi.ac.uk/efo/EFO_0005674 GCST004991 Genome-wide genotyping array 2017-12-01 28924203 Ren HY 2017-09-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28924203 The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. Abnormal white matter microstructure in first episode schizophrenia (multivariate analysis) 93 Han Chinese cases, 134 Han Chinese controls NA Illumina [6055918] (imputed) 1 parietal cortex measurement, white matter microstructure measurement, cingulate cortex measurement http://www.ebi.ac.uk/efo/EFO_0008420, http://www.ebi.ac.uk/efo/EFO_0005674, http://www.ebi.ac.uk/efo/EFO_0007738 GCST004997 Genome-wide genotyping array 2017-12-01 28924203 Ren HY 2017-09-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28924203 The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. White matter microstructure in first episode schizophrenia (left anterior cingulate cortex) 93 Han Chinese cases, 134 Han Chinese controls NA Illumina [6055918] (imputed) 1 white matter microstructure measurement, cingulate cortex measurement http://www.ebi.ac.uk/efo/EFO_0005674, http://www.ebi.ac.uk/efo/EFO_0007738 GCST004994 Genome-wide genotyping array 2017-12-01 28924203 Ren HY 2017-09-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28924203 The common variants implicated in microstructural abnormality of first episode and drug-naïve patients with schizophrenia. White matter microstructure in first episode schizophrenia (right anterior cingulate cortex) 93 Han Chinese cases, 134 Han Chinese controls NA Illumina [6055918] (imputed) 1 white matter microstructure measurement, cingulate cortex measurement http://www.ebi.ac.uk/efo/EFO_0005674, http://www.ebi.ac.uk/efo/EFO_0007738 GCST004993 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Lipoprotein-associated phospholipase A2 activity change in response to darapladib treatment in cardiovascular disease (adjusted for baseline) 10,874 European, Asian, African, Arabic, Native American, Pacific Islander and other ancestry NA Affymetrix, Illumina [13572687] (imputed) 0 response to darapladib, lipoprotein-associated phospholipase A(2) change measurement http://www.ebi.ac.uk/efo/EFO_0008395, http://www.ebi.ac.uk/efo/EFO_0008432 GCST004968 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Lipoprotein-associated phospholipase A2 activity change in response to darapladib treatment in cardiovascular disease 10,874 European, Asian, African, Arabic, Native American, Pacific Islander and other ancestry NA Affymetrix, Illumina [13572687] (imputed) 3 response to darapladib, lipoprotein-associated phospholipase A(2) change measurement http://www.ebi.ac.uk/efo/EFO_0008395, http://www.ebi.ac.uk/efo/EFO_0008432 GCST004966 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Major coronary event in placebo-treated cardiovascular disease (time to event) 1,440 European, African American, Asian and other ancestry cases NA Affymetrix, Illumina [9334585] (imputed) 2 cardiovascular event measurement, response to placebo http://www.ebi.ac.uk/efo/EFO_0006919, http://www.ebi.ac.uk/efo/EFO_0008344 GCST004961 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Diarrhoea in darapladib-treated cardiovascular disease (time to event) 481 European ancestry cases NA Affymetrix, Illumina [9334585] (imputed) 3 response to darapladib, Diarrhea http://www.ebi.ac.uk/efo/EFO_0008395, http://purl.obolibrary.org/obo/HP_0002014 GCST004962 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Myocardial infarction in darapladib-treated cardiovascular disease (time to event) 740 European, African American, Asian and other ancestry cases NA Affymetrix, Illumina [9334585] (imputed) 2 response to darapladib, myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008395, http://www.ebi.ac.uk/efo/EFO_0000612 GCST004964 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Myocardial infarction in placebo-treated cardiovascular disease (time to event) 833 European, African American, Asian and other ancestry cases NA Affymetrix, Illumina [9334585] (imputed) 0 myocardial infarction, response to placebo http://www.ebi.ac.uk/efo/EFO_0000612, http://www.ebi.ac.uk/efo/EFO_0008344 GCST004965 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Major coronary event in cardiovascular disease (time to event) (darapladib treatment interaction) 1,318 European, African American, Asian and other ancestry darapladib-treated cases, 1,440 European, African American, Asian and other ancestry placebo-treated cases NA Affymetrix, Illumina [9334585] (imputed) 5 response to darapladib, cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0008395, http://www.ebi.ac.uk/efo/EFO_0006919 GCST004958 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Odor events in darapladib-treated cardiovascular disease (time to event) 1,867 European, African American, Asian and other ancestry cases NA Affymetrix, Illumina [9334585] (imputed) 0 response to darapladib, body odor measurement http://www.ebi.ac.uk/efo/EFO_0008395, http://www.ebi.ac.uk/efo/EFO_0008386 GCST004960 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Major coronary event in darapladib-treated cardiovascular disease (time to event) 1,318 European, African American, Asian and other ancestry cases NA Affymetrix, Illumina [9334585] (imputed) 2 response to darapladib, cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0008395, http://www.ebi.ac.uk/efo/EFO_0006919 GCST004957 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Lipoprotein phospholipase A2 activity in cardiovascular disease 22,156 European, Asian, African, Arabic, Native American, Pacific Islander and other ancestry NA Affymetrix, Illumina [13572687] (imputed) 16 lipoprotein-associated phospholipase A(2) measurement http://www.ebi.ac.uk/efo/EFO_0004746 GCST004963 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Myocardial infarction in cardiovascular disease (time to event) (darapladib treatment interaction) 740 European, African American, Asian and other ancestry darapladib-treated cases, 833 European, African American, Asian and other ancestry placebo-treated cases NA Affymetrix, Illumina [9334585] (imputed) 1 response to darapladib, myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008395, http://www.ebi.ac.uk/efo/EFO_0000612 GCST004959 Genome-wide genotyping array 2017-11-20 28753643 Yeo A 2017-07-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28753643 Pharmacogenetic meta-analysis of baseline risk factors, pharmacodynamic, efficacy and tolerability endpoints from two large global cardiovascular outcomes trials for darapladib. Moderate or severe diarrhoea in darapladib-treated cardiovascular disease (time to event) 212 European ancestry cases NA Affymetrix, Illumina [9334585] (imputed) 7 response to darapladib, Diarrhea http://www.ebi.ac.uk/efo/EFO_0008395, http://purl.obolibrary.org/obo/HP_0002014 GCST004967 Genome-wide genotyping array 2017-12-01 29071344 Zhou H 2017-10-25 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/29071344 Genetic Risk Variants Associated With Comorbid Alcohol Dependence and Major Depression. Major depression and alcohol dependence 3,041 African American individuals, 1,618 European ancestry individuals 1,612 African American individuals, 1,551 European ancestry individuals Illumina [at least 5086170] (imputed) 47 unipolar depression, alcohol dependence http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0007079 GCST005022 Genome-wide genotyping array 2018-01-09 29059430 Morton LM 2017-11-01 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/29059430 Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer. Breast cancer in childhood cancer survivors treated with less than 10 gray radiotherapy 69 European ancestry cases, 2,144 European ancestry controls NA Affymetrix, Illumina [16958466] (imputed) 3 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST005110 Genome-wide genotyping array 2018-01-09 29059430 Morton LM 2017-11-01 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/29059430 Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer. Breast cancer in childhood cancer survivors treated with more than 10 gray radiotherapy 131 European ancestry cases, 493 European ancestry controls NA Affymetrix, Illumina [16958466] (imputed) 3 response to radiation, breast carcinoma http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0000305 GCST005112 Genome-wide genotyping array 2018-01-09 29059430 Morton LM 2017-11-01 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/29059430 Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer. Breast cancer in childhood cancer survivors 207 European ancestry female cases, 2,774 European ancestry female controls NA Affymetrix, Illumina [16958466] (imputed) 5 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST005111 Genome-wide genotyping array 2017-11-30 29058377 Sanchez-Roige S 2017-10-23 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29058377 Genome-wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry. Alcohol consumption over the past year 20,328 European ancestry individuals NA Illumina [13280794] (imputed) 5 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST004990 Genome-wide genotyping array 2018-03-05 29367611 Gao B 2018-01-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29367611 Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer. Paclitaxel disposition in epithelial ovarian cancer 66 European ancestry cases, 14 Asian ancestry cases NA Illumina [610255] 31 methylcobalamin deficiency type cblE http://purl.obolibrary.org/obo/MONDO_0009354 GCST005352 Genome-wide genotyping array 2018-03-05 29367611 Gao B 2018-01-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29367611 Genome-wide association study of paclitaxel and carboplatin disposition in women with epithelial ovarian cancer. Carboplatin disposition in epthelial ovarian cancer 42 European ancestry cases, 14 Asian ancestry cases NA Illumina [610255] 18 response to carboplatin http://purl.obolibrary.org/obo/GO_0097328 GCST005351 Genome-wide genotyping array 2018-02-02 29082582 Almli LM 2017-10-30 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29082582 Problematic alcohol use associates with sodium channel and clathrin linker 1 (SCLT1) in trauma-exposed populations. Problematic alcohol use in trauma-exposed individuals 1,036 African American individuals 828 European ancestry individuals, 108 African ancestry individuals, 282 Hispanic and Native American individuals, 170 other ancestry individuals, 6 Asian individuals Illumina [501278] 5 alcohol use disorder measurement, response to trauma exposure http://www.ebi.ac.uk/efo/EFO_0009458, http://www.ebi.ac.uk/efo/EFO_0008483 GCST005236 Genome-wide genotyping array 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Body mass index x sex interaction up to 142,613 European ancestry men, up to 167,276 European ancestry women NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 0 sex interaction measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004340 GCST005949 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Body mass index x sex x age interaction (4df test) up to 51,625 European ancestry men aged <50, up to 60,654 European ancestry women aged <50, up to 90,988 European ancestry men aged >50, up to 106,622 European ancestry women aged >50 NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 15 sex interaction measurement, body mass index, age at assessment http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0008007 GCST005950 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Body mass index up to 309,889 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 200 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST005951 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Body mass index (age>50) up to 90,988 European ancestry men, up to 106,622 European ancestry women NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 8 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST005952 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Body mass index (age <50) up to 51,625 European ancestry men, up to 60,654 European ancestry women NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 11 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST005953 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Body mass index x age interaction up to 112,279 European ancestry individuals aged <50, up to 197,610 European ancestry individuals aged >50 NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 5 body mass index, age at assessment http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0008007 GCST005954 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Body mass index x sex x age interaction up to 51,625 European ancestry men aged <50, up to 60,654 European ancestry women aged <50, up to 90,988 European ancestry men aged >50, up to 106,622 European ancestry women aged >50 NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 0 sex interaction measurement, body mass index, age at assessment http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0008007 GCST005955 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Waist-to-hip ratio adjusted for BMI up to 113,720 European ancestry men, up to 138,655 European ancestry women NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 84 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST005956 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Waist-to-hip ratio adjusted for BMI (age <50) up to 43,776 European ancestry men, up to 50,526 European ancestry women NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 15 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST005957 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Waist-to-hip ratio adjusted for BMI (age >50) up to 69,944 European ancestry men, up to 88,129 European ancestry women NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 20 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST005958 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Waist-to-hip ratio adjusted for BMI x sex interaction up to 113,720 European ancestry men, up to 138,655 European ancestry women NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 33 BMI-adjusted waist-hip ratio, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0008343 GCST005959 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Waist-to-hip ratio adjusted for BMI x sex x age interaction up to 43,776 European ancestry men aged <50, up to 50,526 European ancestry women aged <50, up to 69,944 European ancestry men aged >50, up to 88,129 European ancestry women aged >50 NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 0 BMI-adjusted waist-hip ratio, sex interaction measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0008007 GCST005960 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Waist-to-hip ratio adjusted for BMI x age interaction up to 94,302 European ancestry individuals aged <50, up to 158,073 European ancestry individuals aged >50 NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 0 BMI-adjusted waist-hip ratio, age at assessment http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0008007 GCST005961 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-07-24 26426971 Winkler TW 2015-10-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26426971 The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study. Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test) up to 43,776 European ancestry men aged <50, up to 50,526 European ancestry women aged <50, up to 69,944 European ancestry men aged >50, up to 88,129 European ancestry women aged >50 NA Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 85 BMI-adjusted waist-hip ratio, sex interaction measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0008007 GCST005962 Genome-wide genotyping array, Targeted genotyping array [Metabochip, CardioMetabochip] 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Systolic blood pressure x smoking status (current vs non-current) interaction (1df test) 14,607 European ancestry current smokers, 65,935 European ancestry former and never smokers, 5,545 African ancestry current smokers, 21,571 African ancestry former and never smokers, 2,465 Asian ancestry current smokers, 10,973 Asian ancestry former and never smokers, 1,068 Hispanic current smokers, 7,737 Hispanic former and never smokers 48,198 European ancestry current smokers, 251,872 European ancestry former and never smokers, 1,971 African ancestry current smokers, 5,814 African ancestry former and never smokers, 29,485 Asian ancestry current smokers, 119,447 Asian ancestry former and never smokers, 3,737 Hispanic current smokers, 14,199 Hispanic former and never smokers Affymetrix, Illumina [18800000] (imputed) 9 smoking status measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006335 GCST006186 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Systolic blood pressure x smoking status (current vs non-current) interaction (2df test) 14,607 European ancestry current smokers, 65,935 European ancestry former and never smokers, 5,545 African ancestry current smokers, 21,571 African ancestry former and never smokers, 2,465 Asian ancestry current smokers, 10,973 Asian ancestry former and never smokers, 1,068 Hispanic current smokers, 7,737 Hispanic former and never smokers 48,198 European ancestry current smokers, 251,872 European ancestry former and never smokers, 1,971 African ancestry current smokers, 5,814 African ancestry former and never smokers, 29,485 Asian ancestry current smokers, 119,447 Asian ancestry former and never smokers, 3,737 Hispanic current smokers, 14,199 Hispanic former and never smokers Affymetrix, Illumina [18800000] (imputed) 95 smoking status measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006335 GCST006195 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Diastolic blood pressure x smoking status (current vs non-current) interaction (1df test) 14,607 European ancestry current smokers, 65,935 European ancestry former and never smokers, 5,545 African ancestry current smokers, 21,571 African ancestry former and never smokers, 2,465 Asian ancestry current smokers, 10,973 Asian ancestry former and never smokers, 1,068 Hispanic current smokers, 7,737 Hispanic former and never smokers 48,198 European ancestry current smokers, 251,872 European ancestry former and never smokers, 1,971 African ancestry current smokers, 5,814 African ancestry former and never smokers, 29,485 Asian ancestry current smokers, 119,447 Asian ancestry former and never smokers, 3,737 Hispanic current smokers, 14,199 Hispanic former and never smokers Affymetrix, Illumina [18800000] (imputed) 9 smoking status measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006336 GCST006194 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Diastolic blood pressure x smoking status (current vs non-current) interaction (2df test) 14,607 European ancestry current smokers, 65,935 European ancestry former and never smokers, 5,545 African ancestry current smokers, 21,571 African ancestry former and never smokers, 2,465 Asian ancestry current smokers, 10,973 Asian ancestry former and never smokers, 1,068 Hispanic current smokers, 7,737 Hispanic former and never smokers 48,198 European ancestry current smokers, 251,872 European ancestry former and never smokers, 1,971 African ancestry current smokers, 5,814 African ancestry former and never smokers, 29,485 Asian ancestry current smokers, 119,447 Asian ancestry former and never smokers, 3,737 Hispanic current smokers, 14,199 Hispanic former and never smokers Affymetrix, Illumina [18800000] (imputed) 97 smoking status measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006336 GCST006193 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Systolic blood pressure x smoking status (ever vs never) interaction (2df test) 43,016 European ancestry ever smokers, 37,535 European ancestry never smokers, 12,693 African ancestry ever smokers, 13,121 African ancestry never smokers, 4,142 Asian ancestry ever smokers, 9,296 Asian ancestry never smokers, 3,228 Hispanic ever smokers, 5,577 Hispanic never smokers 139,127 European ancestry ever smokers, 145,914 European ancestry never smokers, 3,105 African ancestry ever smokers, 3,075 African ancestry never smokers, 70,335 Asian ancestry ever smokers, 78,597 Asian ancestry never smokers, 6,810 Hispanic ever smokers, 11,133 Hispanic never smokers Affymetrix, Illumina [18800000] (imputed) 88 smoking status measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006335 GCST006192 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Diastolic blood pressure x smoking status (ever vs never) interaction (1df test) 43,016 European ancestry ever smokers, 37,535 European ancestry never smokers, 12,693 African ancestry ever smokers, 13,121 African ancestry never smokers, 4,142 Asian ancestry ever smokers, 9,296 Asian ancestry never smokers, 3,228 Hispanic ever smokers, 5,577 Hispanic never smokers 139,127 European ancestry ever smokers, 145,914 European ancestry never smokers, 3,105 African ancestry ever smokers, 3,075 African ancestry never smokers, 70,335 Asian ancestry ever smokers, 78,597 Asian ancestry never smokers, 6,810 Hispanic ever smokers, 11,133 Hispanic never smokers Affymetrix, Illumina [18800000] (imputed) 2 smoking status measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006336 GCST006191 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Diastolic blood pressure x smoking status (ever vs never) interaction (2df test) 43,016 European ancestry ever smokers, 37,535 European ancestry never smokers, 12,693 African ancestry ever smokers, 13,121 African ancestry never smokers, 4,142 Asian ancestry ever smokers, 9,296 Asian ancestry never smokers, 3,228 Hispanic ever smokers, 5,577 Hispanic never smokers 139,127 European ancestry ever smokers, 145,914 European ancestry never smokers, 3,105 African ancestry ever smokers, 3,075 African ancestry never smokers, 70,335 Asian ancestry ever smokers, 78,597 Asian ancestry never smokers, 6,810 Hispanic ever smokers, 11,133 Hispanic never smokers Affymetrix, Illumina [18800000] (imputed) 91 smoking status measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006336 GCST006190 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Systolic blood pressure x smoking status (ever vs never) interaction (1df test) 43,016 European ancestry ever smokers, 37,535 European ancestry never smokers, 12,693 African ancestry ever smokers, 13,121 African ancestry never smokers, 4,142 Asian ancestry ever smokers, 9,296 Asian ancestry never smokers, 3,228 Hispanic ever smokers, 5,577 Hispanic never smokers 139,127 European ancestry ever smokers, 145,914 European ancestry never smokers, 3,105 African ancestry ever smokers, 3,075 African ancestry never smokers, 70,335 Asian ancestry ever smokers, 78,597 Asian ancestry never smokers, 6,810 Hispanic ever smokers, 11,133 Hispanic never smokers Affymetrix, Illumina [18800000] (imputed) 0 smoking status measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006335 GCST006189 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Systolic blood pressure (cigarette smoking interaction) 80,552 European ancestry individuals, 27,118 African individuals, 13,438 Asian individuals, 8,805 Hispanic individuals 305,513 European ancestry individuals, 7,786 African individuals, 148,932 Asian individuals, 13,533 Hispanic individuals, 4,414 Brazilian individuals Affymetrix, Illumina [18800000] (imputed) 46 smoking status measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006335 GCST006188 Genome-wide genotyping array 2018-09-05 29455858 Sung YJ 2018-02-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29455858 A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure. Diastolic blood pressure (cigarette smoking interaction) 80,552 European ancestry individuals, 27,118 African individuals, 13,438 Asian individuals, 8,805 Hispanic individuals 305,513 European ancestry individuals, 7,786 African individuals, 148,932 Asian individuals, 13,533 Hispanic individuals, 4,414 Brazilian individuals Affymetrix, Illumina [18800000] (imputed) 45 smoking status measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006336 GCST006187 Genome-wide genotyping array 2018-07-11 29497042 Verweij N 2018-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29497042 Genetic study links components of the autonomous nervous system to heart-rate profile during exercise. Heart rate increase in response to exercise 5,4137 European ancestry individuals, 1,744 Asian ancestry individuals, 1,445 African ancestry individuals, 468 admixed individuals, 1,024 individuals NA Affymetrix [509255] (imputed) 11 heart rate response to exercise http://www.ebi.ac.uk/efo/EFO_0009184 GCST005845 Genome-wide genotyping array 2018-07-11 29497042 Verweij N 2018-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29497042 Genetic study links components of the autonomous nervous system to heart-rate profile during exercise. Heart rate response to recovery post exercise (30 sec) 5,4137 European ancestry individuals, 1,744 Asian individuals, 1,445 African individuals, 468 admixed individuals, 1,024 individuals NA Affymetrix [509255] (imputed) 14 heart rate response to recovery post exercise http://www.ebi.ac.uk/efo/EFO_0009185 GCST005850 Genome-wide genotyping array 2018-07-11 29497042 Verweij N 2018-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29497042 Genetic study links components of the autonomous nervous system to heart-rate profile during exercise. Heart rate response to recovery post exercise (40 sec) 5,4137 European ancestry individuals, 1,744 Asian individuals, 1,445 African individuals, 468 admixed individuals, 1,024 individuals NA Affymetrix [509255] (imputed) 14 heart rate response to recovery post exercise http://www.ebi.ac.uk/efo/EFO_0009185 GCST005849 Genome-wide genotyping array 2018-07-11 29497042 Verweij N 2018-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29497042 Genetic study links components of the autonomous nervous system to heart-rate profile during exercise. Heart rate response to recovery post exercise (50 sec) 5,4137 European ancestry individuals, 1,744 Asian individuals, 1,445 African individuals, 468 admixed individuals, 1,024 individuals NA Affymetrix [509255] (imputed) 18 heart rate response to recovery post exercise http://www.ebi.ac.uk/efo/EFO_0009185 GCST005848 Genome-wide genotyping array 2018-07-11 29497042 Verweij N 2018-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29497042 Genetic study links components of the autonomous nervous system to heart-rate profile during exercise. Heart rate response to recovery post exercise (10 sec) 5,4137 European ancestry individuals, 1,744 Asian individuals, 1,445 African individuals, 468 admixed individuals, 1,024 individuals NA Affymetrix [509255] (imputed) 15 heart rate response to recovery post exercise http://www.ebi.ac.uk/efo/EFO_0009185 GCST005846 Genome-wide genotyping array 2018-07-11 29497042 Verweij N 2018-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29497042 Genetic study links components of the autonomous nervous system to heart-rate profile during exercise. Heart rate response to recovery post exercise (20 sec) 5,4137 European ancestry individuals, 1,744 Asian individuals, 1,445 African individuals, 468 admixed individuals, 1,024 individuals NA Affymetrix [509255] (imputed) 16 heart rate response to recovery post exercise http://www.ebi.ac.uk/efo/EFO_0009185 GCST005847 Genome-wide genotyping array 2017-07-07 28440896 Yin X 2017-04-25 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28440896 Genome-wide meta-analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence. Nicotine dependence 7,297 European ancestry cases, 5,577 European ancestry controls, 918 European ancestry whole genome sequenced cases, 921 European ancestry whole genome sequenced controls, African American cases, 1,500 African American controls NA Illumina [at least 3251541] (imputed) 14 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST004294 Genome-wide genotyping array 2017-11-24 29117387 Conti DV 2017-08-01 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/29117387 Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry. Prostate cancer 5,454 African American cases, 474 West African cases, 4,274 African American and African ancestry cases, 6,328 African American controls, 458 West African controls, 4,024 African American and African ancestry controls NA Affymetrix, Illumina [17013228] (imputed) 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST004982 Genome-wide genotyping array 2018-01-17 29208002 Kim M 2017-12-06 Lipids Health Dis www.ncbi.nlm.nih.gov/pubmed/29208002 EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population. Diastolic blood pressure 2146 East Asian ancestry individuals NA Affymetrix [394222] 6 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST005169 Genome-wide genotyping array 2018-01-17 29208002 Kim M 2017-12-06 Lipids Health Dis www.ncbi.nlm.nih.gov/pubmed/29208002 EPHA6 rs4857055 C > T polymorphism associates with hypertension through triglyceride and LDL particle size in the Korean population. Systolic blood pressure 2146 East Asian ancestry individuals NA Affymetrix [394222] 6 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST005168 Genome-wide genotyping array 2017-11-27 29058489 Ogata S 2017-10-23 Clin Exp Hypertens www.ncbi.nlm.nih.gov/pubmed/29058489 Genome-wide association study for white coat effect in Japanese middle-aged to elderly people: The HOMED-BP study. White coat effect (clinic systolic blood pressure minus home systolic blood pressure) 295 Japanese ancestry individuals 236 Japanese ancestry individuals Affymetrix [6901629] (imputed) 0 response to stress, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0006950, http://www.ebi.ac.uk/efo/EFO_0006944 GCST004984 Genome-wide genotyping array 2017-11-27 29058489 Ogata S 2017-10-23 Clin Exp Hypertens www.ncbi.nlm.nih.gov/pubmed/29058489 Genome-wide association study for white coat effect in Japanese middle-aged to elderly people: The HOMED-BP study. White coat effect (clinic diastolic blood pressure minus home diastolic blood pressure) 295 Japanese ancestry individuals 236 Japanese ancestry individuals Affymetrix [6901629] (imputed) 0 diastolic blood pressure change measurement, response to stress http://www.ebi.ac.uk/efo/EFO_0006945, http://purl.obolibrary.org/obo/GO_0006950 GCST004985 Genome-wide genotyping array 2017-09-21 28754176 Wang Z 2017-07-28 Environ Health www.ncbi.nlm.nih.gov/pubmed/28754176 Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment. Motor development (prenatal lead exposure interaction) 390 Mexican children, 490 Bangladeshi children NA Illumina [552487] 1 motor development measurement, blood lead measurement http://www.ebi.ac.uk/efo/EFO_0008237, http://www.ebi.ac.uk/efo/EFO_0007040 GCST004768 Genome-wide genotyping array 2017-09-21 28754176 Wang Z 2017-07-28 Environ Health www.ncbi.nlm.nih.gov/pubmed/28754176 Genome-wide gene by lead exposure interaction analysis identifies UNC5D as a candidate gene for neurodevelopment. Mental development (prenatal lead exposure interaction) 390 Mexican children, 490 Bangladeshi children NA Illumina [552487] 1 blood lead measurement, mental development measurement http://www.ebi.ac.uk/efo/EFO_0007040, http://www.ebi.ac.uk/efo/EFO_0008230 GCST004769 Genome-wide genotyping array 2018-03-23 29364747 Jonsson L 2018-01-01 J Dent Res www.ncbi.nlm.nih.gov/pubmed/29364747 Rare and Common Variants Conferring Risk of Tooth Agenesis. Tooth agenesis 1,944 Icelandic ancestry cases, 338,554 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) 151 European ancestry cases, 6,019 European ancestry controls, 150 European and other ancestry cases, 2,696 European and other ancestry controls Illumina [NR] (imputed) 4 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST005389 Genome-wide genotyping array 2018-03-23 29364747 Jonsson L 2018-01-01 J Dent Res www.ncbi.nlm.nih.gov/pubmed/29364747 Rare and Common Variants Conferring Risk of Tooth Agenesis. Tooth agenesis (mandibular second premolars) 1,196 Icelandic ancestry cases, 338,554 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) 66 European ancestry cases, 4,667 European ancestry controls, 82 European and other ancestry cases, 2,696 European and other ancestry controls Illumina [NR] (imputed) 1 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST005390 Genome-wide genotyping array 2018-03-23 29364747 Jonsson L 2018-01-01 J Dent Res www.ncbi.nlm.nih.gov/pubmed/29364747 Rare and Common Variants Conferring Risk of Tooth Agenesis. Tooth agenesis (maxillary lateral incisors) 600 Icelandic ancestry cases, 338,554 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) 102 European ancestry cases, 204 European ancestry controls, 32 European and other ancestry cases, 2,696 European and other ancestry controls Illumina [NR] (imputed) 2 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST005391 Genome-wide genotyping array 2018-03-23 29364747 Jonsson L 2018-01-01 J Dent Res www.ncbi.nlm.nih.gov/pubmed/29364747 Rare and Common Variants Conferring Risk of Tooth Agenesis. Tooth agenesis (maxillary second premolars) 600 Icelandic ancestry cases, 338,554 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [NR] (imputed) 1 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST005392 Genome-wide genotyping array 2017-08-11 28520984 Saccone NL 2017-05-17 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/28520984 Genome-wide association study of heavy smoking and daily/nondaily smoking in the Hispanic Community Health Study / Study of Latinos (HCHS/SOL). Smoking status (daily vs non-daily) 778 Hispanic non-daily smoker cases, 1,786 Hispanic daily smoker controls 85 Hispanic non-daily smokers, 343 Hispanic daily smokers, 158 African American non-daily smokers, 1,106 African American daily smokers, 232 European ancestry non-daily smokers, 1,316 European ancestry daily smokers Illumina [at least 2400000] (imputed) 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST004511 Genome-wide genotyping array 2017-08-11 28520984 Saccone NL 2017-05-17 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/28520984 Genome-wide association study of heavy smoking and daily/nondaily smoking in the Hispanic Community Health Study / Study of Latinos (HCHS/SOL). Smoking status (heavy vs light) 1,929 Hispanic heavy smoker cases, 3,156 Hispanic light smoker controls NA Illumina [~ 11400000] (imputed) 2 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST004512 Genome-wide genotyping array 2017-08-11 28520984 Saccone NL 2017-05-17 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/28520984 Genome-wide association study of heavy smoking and daily/nondaily smoking in the Hispanic Community Health Study / Study of Latinos (HCHS/SOL). Smoking status (current vs former) 2,564 Hispanic current smoker cases, 2,555 Hispanic former smoker controls NA Illumina [at least 2400000] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST004513 Genome-wide genotyping array 2017-08-11 28520984 Saccone NL 2017-05-17 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/28520984 Genome-wide association study of heavy smoking and daily/nondaily smoking in the Hispanic Community Health Study / Study of Latinos (HCHS/SOL). Smoking status (ever vs never smokers) 5,119 Hispanic ever smoker cases, 7,616 Hispanic never smoker controls NA Illumina [at least 2400000] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST004514 Genome-wide genotyping array 2017-09-05 28584135 Chaturvedi S 2017-06-05 Blood www.ncbi.nlm.nih.gov/pubmed/28584135 Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia. Vaso-occlusive pain in sickle-cell anemia 359 African ancestry individuals, 934 African ancestry children Illumina [1098907] (imputed) 1 vaso-occlusive pain measurement http://www.ebi.ac.uk/efo/EFO_0008316 GCST004644 Genome-wide genotyping array 2017-09-22 28566273 Scott RA 2017-05-31 Diabetes www.ncbi.nlm.nih.gov/pubmed/28566273 An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. Type 2 diabetes up to 26,676 European ancestry cases, up to 132,532 European ancestry controls 14,545 European ancestry cases, 38,994 European ancestry controls Affymetrix, Illumina [at least 11579618] (imputed) 24 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004773 Genome-wide genotyping array, Targeted genotyping array 2017-09-22 28566273 Scott RA 2017-05-31 Diabetes www.ncbi.nlm.nih.gov/pubmed/28566273 An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. Type 2 diabetes up to 26,676 European ancestry cases, up to 132,532 European ancestry controls up to 12,543 European ancestry cases, up to 66,458 European ancestry controls Affymetrix, Illumina [at least 11579618] (imputed) 12 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004774 Genome-wide genotyping array 2017-09-15 28662289 Lin YY 2017-06-29 Cancer www.ncbi.nlm.nih.gov/pubmed/28662289 Genome-wide association analysis identifies a GLUL haplotype for familial hepatitis B virus-related hepatocellular carcinoma. Familial hepatitis B virus-related hepatocellular carcinoma 139 East Asian ancestry cases, 139 East Asian ancestry controls NA Affymetrix [641398] 4 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST004736 Genome-wide genotyping array 2017-07-21 28577822 Deters KD 2017-05-31 Brain Lang www.ncbi.nlm.nih.gov/pubmed/28577822 Genome-wide association study of language performance in Alzheimer's disease. Language performance in older adults (adjusted for episodic memory) 310 European ancestry Alzheimer's disease individuals, 511 European ancestry individuals with late mild cognitive impairment, 280 European ancestry individuals with early mild cognitive impairment, 94 European ancestry individuals with significant memory concern, 365 European ancestry individuals with normal cognition NA Illumina [5574300] (imputed) 8 cognitive decline measurement, memory performance, language measurement http://www.ebi.ac.uk/efo/EFO_0007710, http://www.ebi.ac.uk/efo/EFO_0004874, http://www.ebi.ac.uk/efo/EFO_0007797 GCST004372 Genome-wide genotyping array 2018-04-25 22057235 Trynka G 2011-11-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22057235 Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Celiac disease 11,812 European ancestry cases, 229 Indian ancestry cases, 11,837 European ancestry controls, 391 Indian ancestry controls NA Illumina [139553] 43 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST005523 Targeted genotyping array [ImmunoChip] 2017-12-05 28990592 Warrington NM 2017-10-09 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/28990592 Maternal and fetal genetic contribution to gestational weight gain. Early gestational weight gain (fetal effect) up to 8,559 European ancestry fetuses up to 3,289 European ancestry fetuses Affymetrix, Illumina [NR] (imputed) 0 early gestational weight gain, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0008437, http://www.ebi.ac.uk/efo/EFO_0007959 GCST005032 Genome-wide genotyping array 2017-12-05 28990592 Warrington NM 2017-10-09 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/28990592 Maternal and fetal genetic contribution to gestational weight gain. Gestational weight gain (fetal effect) up to 16,434 European ancestry fetuses up to 7,827 European ancestry fetuses Affymetrix, Illumina [NR] (imputed) 0 fetal genotype effect measurement, gestational weight gain measurement http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0008435 GCST005031 Genome-wide genotyping array 2017-12-05 28990592 Warrington NM 2017-10-09 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/28990592 Maternal and fetal genetic contribution to gestational weight gain. Late gestational weight gain (fetal effect) up to 8,641 European ancestry fetuses up to 779 European ancestry fetuses Affymetrix, Illumina [NR] (imputed) 0 fetal genotype effect measurement, late gestational weight gain http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0008436 GCST005030 Genome-wide genotyping array 2017-12-05 28990592 Warrington NM 2017-10-09 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/28990592 Maternal and fetal genetic contribution to gestational weight gain. Early gestation weight gain (maternal effect) up to 7,704 European ancestry mothers up to 1,584 European ancestry mothers Affymetrix, Illumina [NR] (imputed) 0 early gestational weight gain http://www.ebi.ac.uk/efo/EFO_0008437 GCST005029 Genome-wide genotyping array 2017-12-05 28990592 Warrington NM 2017-10-09 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/28990592 Maternal and fetal genetic contribution to gestational weight gain. Late gestational weight gain (maternal effect) up to 7,681 European ancestry mothers up to 1,646 European ancestry mothers Affymetrix, Illumina [NR] (imputed) 0 late gestational weight gain http://www.ebi.ac.uk/efo/EFO_0008436 GCST005034 Genome-wide genotyping array 2017-12-05 28990592 Warrington NM 2017-10-09 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/28990592 Maternal and fetal genetic contribution to gestational weight gain. Gestational weight gain (maternal effect) up to 10,555 European ancestry mothers up to 11280 European ancestry mothers Affymetrix, Illumina [NR] (imputed) 0 gestational weight gain measurement http://www.ebi.ac.uk/efo/EFO_0008435 GCST005033 Genome-wide genotyping array 2018-01-08 29186428 Tonjes A 2017-11-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29186428 Genome-wide meta-analysis identifies novel determinants of circulating serum progranulin. Progranulin levels 1,963 European ancestry individuals, 848 Sorbian (founder/genetic isolate) individuals 1800 European ancestry individuals Affymetrix [2069113] (imputed) 3 progranulin measurement http://www.ebi.ac.uk/efo/EFO_0004625 GCST005109 Genome-wide genotyping array 2017-09-26 27723757 Jin Y 2016-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27723757 Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. Vitiligo 2,853 European ancestry cases and 37,405 European ancestry controls 1,827 European ancestry cases and 2,181 European ancestry controls Illumina [8966411] (imputed) 57 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST004785 Genome-wide genotyping array 2018-02-02 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Caudate volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 2 response to trauma exposure, caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0004830 GCST005240 Genome-wide genotyping array 2018-02-02 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Nucleus accumbens volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 4 response to trauma exposure, nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0006931 GCST005241 Genome-wide genotyping array 2018-02-02 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Pallidum volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 1 pallidum volume, response to trauma exposure http://www.ebi.ac.uk/efo/EFO_0006933, http://www.ebi.ac.uk/efo/EFO_0008483 GCST005242 Genome-wide genotyping array 2018-02-02 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Amygdala volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 0 response to trauma exposure, amygdala volume http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0006934 GCST005239 Genome-wide genotyping array 2018-02-02 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Hippocampal volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 0 response to trauma exposure, hippocampal volume http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0005035 GCST005243 Genome-wide genotyping array 2018-02-02 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Putamen volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 0 response to trauma exposure, putamen volume http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0006932 GCST005244 Genome-wide genotyping array 2018-02-12 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Lateral ventricle volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 1 lateral ventricle volume measurement, response to trauma exposure http://www.ebi.ac.uk/efo/EFO_0008487, http://www.ebi.ac.uk/efo/EFO_0008483 GCST005286 Genome-wide genotyping array 2018-02-02 29187748 Morey RA 2017-11-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29187748 Genome-wide association study of subcortical brain volume in PTSD cases and trauma-exposed controls. Thalamus volume in trauma-exposed individuals 36 African American post-traumatic stress disorder cases, 38 African American trauma-exposed controls, 30 European ancestry post-traumatic stress disorder cases, 53 European ancestry trauma-exposed controls NA Illumina [2711511] (imputed) 0 response to trauma exposure, thalamus volume http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0006935 GCST005245 Genome-wide genotyping array 2017-10-09 25608926 Betz RC 2015-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25608926 Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility loci. Alopecia areata 2,332 European ancestry cases and 5,233 European ancestry controls 764 European ancestry cases and 2,256 European ancestry controls Illumina [1233578] (imputed) 33 alopecia areata http://www.ebi.ac.uk/efo/EFO_0004192 GCST004866 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Visceral adipose tissue (sex interaction) 580 Mexican American female individuals, 403 Mexican American male individuals. 365 Mexican American female individuals, 342 Mexican American male individuals Illumina [7708309] (imputed) 0 visceral adipose tissue measurement, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0004765, http://www.ebi.ac.uk/efo/EFO_0008343 GCST005086 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Subcutaneous adipose tissue (sex interaction) 580 Mexican American female individuals, 403 Mexican American male individuals. NA Illumina [7708309] (imputed) 1 subcutaneous adipose tissue measurement, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0004766, http://www.ebi.ac.uk/efo/EFO_0008343 GCST005092 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Subcutaneous adipose tissue 580 Mexican American female individuals, 403 Mexican American male individuals. NA Illumina [7708309] (imputed) 6 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST005091 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Visceral adipose tissue/subcutaneous adipose tissue ratio (sex interaction) 580 Mexican American female individuals, 403 Mexican American male individuals. 365 Mexican American female individuals, 342 Mexican American male individuals Illumina [7708309] (imputed) 0 sex interaction measurement, visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004767 GCST005090 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Visceral adipose tissue/subcutaneous adipose tissue ratio 580 Mexican American female individuals, 403 Mexican American male individuals. 365 Mexican American female individuals, 342 Mexican American male individuals Illumina [7708309] (imputed) 0 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST005089 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Visceral adipose tissue adjusted for BMI (sex interaction) 580 Mexican American female individuals, 403 Mexican American male individuals. 365 Mexican American female individuals, 342 Mexican American male individuals Illumina [7708309] (imputed) 0 visceral adipose tissue measurement, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0004765, http://www.ebi.ac.uk/efo/EFO_0008343 GCST005088 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Visceral adipose tissue adjusted for BMI 580 Mexican American female individuals, 403 Mexican American male individuals. 365 Mexican American female individuals, 342 Mexican American male individuals Illumina [7708309] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST005087 Genome-wide genotyping array 2017-12-20 29178545 Gao C 2017-11-27 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/29178545 Genome-Wide Study of Subcutaneous and Visceral Adipose Tissue Reveals Novel Sex-Specific Adiposity Loci in Mexican Americans. Visceral adipose tissue 580 Mexican American female individuals, 403 Mexican American male individuals. 365 Mexican American female individuals, 342 Mexican American male individuals Illumina [7708309] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST005085 Genome-wide genotyping array 2018-01-12 29186694 Lam M 2017-11-28 Cell Rep www.ncbi.nlm.nih.gov/pubmed/29186694 Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. Cognitive ability 107,207 European ancestry individuals NA Affymetrix, Illumina [7357080] (imputed) 69 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST005142 Genome-wide genotyping array 2018-01-12 29186694 Lam M 2017-11-28 Cell Rep www.ncbi.nlm.nih.gov/pubmed/29186694 Large-Scale Cognitive GWAS Meta-Analysis Reveals Tissue-Specific Neural Expression and Potential Nootropic Drug Targets. Cognitive ability (MTAG) 436,124 European ancestry individuals NA Affymetrix, Illumina, Perlegen [7333576] (imputed) 82 intelligence, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0004784 GCST005141 Genome-wide genotyping array 2019-07-17 25743335 Taylor PN 2015-03-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25743335 Whole-genome sequence-based analysis of thyroid function. Thyroid stimulating hormone levels 2,287 European ancestry whole-genome sequenced individuals, 14,048 European ancestry individuals NA Illumina [at least 9558836] (imputed) 13 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST008165 Genome-wide genotyping array, Genome-wide sequencing 2019-07-17 25743335 Taylor PN 2015-03-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25743335 Whole-genome sequence-based analysis of thyroid function. Free thyroxine concentration 2,287 European ancestry whole-genome sequenced individuals, 11,364 European ancestry individuals NA Illumina [at least 9558836] (imputed) 4 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST008164 Genome-wide genotyping array, Genome-wide sequencing 2017-10-05 28761973 Peng C 2017-07-31 Calcif Tissue Int www.ncbi.nlm.nih.gov/pubmed/28761973 Enhanced Identification of Potential Pleiotropic Genetic Variants for Bone Mineral Density and Breast Cancer. Lumbar spine bone mineral density or breast cancer (pleiotropy) 53,236 individuals with bone mineral density data, 5,152 Chinese ancestry breast cancer cases and controls NA NR [144628] 0 breast carcinoma, spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0007701 GCST004837 Genome-wide genotyping array 2017-10-05 28761973 Peng C 2017-07-31 Calcif Tissue Int www.ncbi.nlm.nih.gov/pubmed/28761973 Enhanced Identification of Potential Pleiotropic Genetic Variants for Bone Mineral Density and Breast Cancer. Femoral neck bone mineral density or breast cancer (pleiotropy) 53,236 individuals with bone mineral density data, 5,152 Chinese ancestry breast cancer cases and controls NA NR [144380] 0 breast carcinoma, femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0007785 GCST004836 Genome-wide genotyping array 2018-08-16 27668658 Iotchkova V 2016-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27668658 Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps. Cardiometabolic and hematological traits up to 35,981 European ancestry individuals up to 102,505 European ancestry individuals Affymetrix, Illumina [17000000] (imputed) 17 hematological measurement http://www.ebi.ac.uk/efo/EFO_0004503 GCST006101 Genome-wide genotyping array 2016-09-20 26482880 Buch S 2015-10-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26482880 A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis. Cirrhosis (alcohol related) 712 European ancestry cases, 1,426 European ancestry alchocol dependent controls 1,148 European ancestry cases, 922 European ancestry alchocol dependent controls Illumina [6770425] (imputed) 3 alcoholic liver cirrhosis http://www.ebi.ac.uk/efo/EFO_1000802 GCST003153 Genome-wide genotyping array 2018-08-10 28373541 Yang J 2017-04-03 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28373541 Genetic signatures of high-altitude adaptation in Tibetans. High altitude adaptation 3,008 Tibetan (founder/genetic isolate) individuals and 7,287 East Asian individuals NA Illumina [7300000] (imputed) 9 high altitude adaptation http://www.ebi.ac.uk/efo/EFO_0009105 GCST006054 Genome-wide genotyping array 2018-03-08 26366551 Zoledziewska M 2015-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26366551 Height-reducing variants and selection for short stature in Sardinia. Height 6,307 Sardinian (founder/population isolate) individuals 5,314 Sardinian (founder/population isolate) individuals, 19,053 European ancestry individuals Illumina [11826948] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST005354 Genome-wide genotyping array 2018-01-19 29221444 Divers J 2017-12-08 BMC Genet www.ncbi.nlm.nih.gov/pubmed/29221444 Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. Coronary artery calcified atherosclerotic plaque (130 HU threshold) in type 2 diabetes 345 African American cases, 346 African American controls 137 African American cases, 68 African American controls Illumina [at least 13000000] (imputed) 84 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST005173 Genome-wide genotyping array 2018-01-19 29221444 Divers J 2017-12-08 BMC Genet www.ncbi.nlm.nih.gov/pubmed/29221444 Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. Coronary artery calcified atherosclerotic plaque score in type 2 diabetes 691 African American individuals 205 African American individuals Illumina [at least 13000000] (imputed) 53 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST005174 Genome-wide genotyping array 2018-01-19 29221444 Divers J 2017-12-08 BMC Genet www.ncbi.nlm.nih.gov/pubmed/29221444 Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. Coronary artery calcified atherosclerotic plaque (90 or 130 HU threshold) in type 2 diabetes 345 African American cases, 346 African American controls 137 African American cases, 68 African American controls Illumina [at least 13000000] (imputed) 68 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST005175 Genome-wide genotyping array 2018-02-02 29313844 Willems SM 2017-07-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29313844 Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Hand grip strength 142,035 European ancestry individuals 53,145 European ancestry individuals Affymetrix [at least 17000000] (imputed) 19 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST005235 Genome-wide genotyping array 2018-02-02 29313844 Willems SM 2017-07-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29313844 Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Fat mass index 12,851 individuals NA Affymetrix [NR] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST005233 Genome-wide genotyping array 2018-02-02 29313844 Willems SM 2017-07-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29313844 Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness. Lean mass index 12,851 individuals NA Affymetrix [at least 17000000] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST005234 Genome-wide genotyping array 2017-10-13 28870582 Wang XF 2017-08-01 J Neurol Sci www.ncbi.nlm.nih.gov/pubmed/28870582 Linking Alzheimer's disease and type 2 diabetes: Novel shared susceptibility genes detected by cFDR approach. Alzheimer's disease or type 2 diabetes (pleiotropy) 17,008 European ancestry Alzheimer's disease cases, 12,171 European ancestry type II diabetes cases, 94,016 European ancestry controls NA NR [262661] (imputed) 0 Alzheimer disease, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/MONDO_0005148 GCST004880 Genome-wide genotyping array 2018-02-21 29317701 Rappoport N 2018-01-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29317701 A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth. Spontaneous preterm birth (preterm birth) 260 European ancestry cases, 190 African-American cases, 745 Hispanic cases, 131 East Asian ancestry cases, 23 South East Asian ancestry cases, 9,630 European ancestry controls, 1,684 African-American controls, 1,102 Hispanic controls, 118 East Asian ancestry controls, 36 South East Asian ancestry controls 145 African American cases, 307 Latino cases, 82 European ancestry cases, 1,274 African American controls, 2,826 Hispanic / Latino controls, 249 European ancestry controls Illumina [2015750] 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST005313 Genome-wide genotyping array 2018-01-19 29253144 Voigt EA 2017-12-14 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/29253144 Polymorphisms in the Wilms Tumor Gene Are Associated With Interindividual Variations in Rubella Virus-Specific Cellular Immunity After Measles-Mumps-Rubella II Vaccination. Rubella-specific interferon-gamma secretion 1,643 European ancestry individuals, 202 African American individuals NA Illumina [NR] (imputed) 0 interferon gamma measurement, response to vaccine http://www.ebi.ac.uk/efo/EFO_0008165, http://www.ebi.ac.uk/efo/EFO_0004645 GCST005177 Genome-wide genotyping array 2018-01-19 29253144 Voigt EA 2017-12-14 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/29253144 Polymorphisms in the Wilms Tumor Gene Are Associated With Interindividual Variations in Rubella Virus-Specific Cellular Immunity After Measles-Mumps-Rubella II Vaccination. Rubella-specific interleukin-6 secretion 1,643 European ancestry individuals, 202 African American individuals NA Illumina [NR] (imputed) 1 interleukin-6 measurement, response to vaccine http://www.ebi.ac.uk/efo/EFO_0004810, http://www.ebi.ac.uk/efo/EFO_0004645 GCST005176 Genome-wide genotyping array 2018-01-26 29195075 Martin AR 2017-11-30 Cell www.ncbi.nlm.nih.gov/pubmed/29195075 An Unexpectedly Complex Architecture for Skin Pigmentation in Africans. Tanning 216 Sub-Saharan African ancestry individuals 240 Sub-Saharan African ancestry individuals Illumina [at least 241929] (imputed) 5 suntan http://www.ebi.ac.uk/efo/EFO_0004279 GCST005189 Genome-wide genotyping array 2018-01-26 29195075 Martin AR 2017-11-30 Cell www.ncbi.nlm.nih.gov/pubmed/29195075 An Unexpectedly Complex Architecture for Skin Pigmentation in Africans. Skin pigmentation 216 Sub-Saharan African ancestry individuals 240 Sub-Saharan African ancestry individuals Illumina [at least 241929] (imputed) 3 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST005188 Genome-wide genotyping array 2017-10-27 28892062 Akiyama M 2017-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28892062 Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. Body mass index up to 72,390 Japanese ancestry women, up to 85,894 Japanese ancestry men up to 10,048 Japanese ancestry women, up to 5,098 Japanese ancestry men, up to 181,999 European ancestry women, up to 140,155 European ancestry controls Illumina [6108953] (imputed) 265 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004904 Genome-wide genotyping array 2017-10-09 28881265 Sobalska-Kwapis M 2017-09-01 Eur J Obstet Gynecol Reprod Biol www.ncbi.nlm.nih.gov/pubmed/28881265 New variants near RHOJ and C2, HLA-DRA region and susceptibility to endometriosis in the Polish population-The genome-wide association study. Endometriosis 171 European ancestry cases, 2,934 European ancestry controls NA Illumina [274400] 32 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST004873 Genome-wide genotyping array 2017-03-24 27723758 Bronson PG 2016-10-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27723758 Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency. Selective IgA deficiency 1,635 European ancestry cases, 4,852 European ancestry controls NA Illumina [up to 9464381] (imputed) 33 selective IgA deficiency disease http://www.ebi.ac.uk/efo/EFO_1001929 GCST003814 Genome-wide genotyping array 2017-09-28 28763429 Serie DJ 2017-07-31 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/28763429 Genome-wide association study of cardiotoxicity in the NCCTG N9831 (Alliance) adjuvant trastuzumab trial. Change in LVEF in response to paclitaxel in HER2+ breast cancer 391 European ancestry cases NA Affymetrix [618793] 0 methylcobalamin deficiency type cblE, left ventricular diastolic function measurement http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0008204 GCST004789 Genome-wide genotyping array 2017-09-28 28763429 Serie DJ 2017-07-31 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/28763429 Genome-wide association study of cardiotoxicity in the NCCTG N9831 (Alliance) adjuvant trastuzumab trial. Change in LVEF in response to paclitaxel and trastuzumab in HER2+ breast cancer 800 European ancestry cases NA Affymetrix [618793] 6 response to trastuzumab, methylcobalamin deficiency type cblE, left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008347, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0008204 GCST004790 Genome-wide genotyping array 2017-09-28 28763429 Serie DJ 2017-07-31 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/28763429 Genome-wide association study of cardiotoxicity in the NCCTG N9831 (Alliance) adjuvant trastuzumab trial. Change in LVEF in response to paclitaxel and in response to paclitaxel and trastuzumab in HER+ breast cancer 1,191 European ancestry cases NA Affymetrix [618793] 0 response to trastuzumab, methylcobalamin deficiency type cblE, left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008347, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0008204 GCST004788 Genome-wide genotyping array 2017-09-14 28672053 Meng W 2017-07-03 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/28672053 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers. Foot ulcer in diabetes and neuropathy 662 European ancestry type 2 diabetes cases, 37 European ancestry type 1 diabetes cases, 2,584 European ancestry type 2 diabetes controls, 111 European ancestry type 1 diabetes controls NA Affymetrix, Illumina [6706850] (imputed) 2 diabetic foot http://www.ebi.ac.uk/efo/EFO_1001459 GCST004724 Genome-wide genotyping array 2017-09-14 28672053 Meng W 2017-07-03 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/28672053 A genome-wide association study suggests that MAPK14 is associated with diabetic foot ulcers. Foot ulcer and neuropathy in diabetes 662 European ancestry type 2 diabetes and neuropathy cases, 37 European ancestry type 1 diabetes and neuropathy cases, 4,250 European ancestry type 1 and type 2 diabetes controls NA Affymetrix, Illumina [6706850] (imputed) 3 diabetic foot, neuropathy http://www.ebi.ac.uk/efo/EFO_1001459, http://www.ebi.ac.uk/efo/EFO_0004149 GCST004725 Genome-wide genotyping array 2017-12-20 29109912 Rawofi L 2017-11-02 PeerJ www.ncbi.nlm.nih.gov/pubmed/29109912 Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. Iris color (b* coordinate) 377 East Asian ancestry individuals NA Illumina [at least 520076] (imputed) 7 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST005096 Genome-wide genotyping array 2017-12-20 29109912 Rawofi L 2017-11-02 PeerJ www.ncbi.nlm.nih.gov/pubmed/29109912 Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. Iris heterochromicity 377 East Asian ancestry individuals NA Illumina [at least 520076] (imputed) 6 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST005095 Genome-wide genotyping array 2017-12-20 29109912 Rawofi L 2017-11-02 PeerJ www.ncbi.nlm.nih.gov/pubmed/29109912 Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. Skin pigmentation 377 East Asian ancestry individuals 568 East Asian ancestry individuals Illumina [at least 520076] (imputed) 0 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST005084 Genome-wide genotyping array 2017-12-20 29109912 Rawofi L 2017-11-02 PeerJ www.ncbi.nlm.nih.gov/pubmed/29109912 Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. Iris color (L* coordinate) 377 East Asian ancestry individuals NA Illumina [at least 520076] (imputed) 14 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST005094 Genome-wide genotyping array 2017-12-20 29109912 Rawofi L 2017-11-02 PeerJ www.ncbi.nlm.nih.gov/pubmed/29109912 Genome-wide association study of pigmentary traits (skin and iris color) in individuals of East Asian ancestry. Iris color (a* coordinate) 377 East Asian ancestry individuals NA Illumina [at least 520076] (imputed) 9 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST005093 Genome-wide genotyping array 2017-09-29 28794112 Christophersen IE 2017-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28794112 Fifteen Genetic Loci Associated With the Electrocardiographic P Wave. P wave terminal force 33,955 European ancestry individuals, 6,778 African individuals NA Affymetrix, Illumina [at least 2402234] (imputed) 12 P wave terminal force measurement http://www.ebi.ac.uk/efo/EFO_0008379 GCST004824 Genome-wide genotyping array 2017-09-29 28794112 Christophersen IE 2017-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28794112 Fifteen Genetic Loci Associated With the Electrocardiographic P Wave. P wave duration 37,678 European ancestry individuals, 6,778 African ancestry individuals NA Affymetrix, Illumina [at least 2402234] (imputed) 20 P wave duration http://www.ebi.ac.uk/efo/EFO_0005094 GCST004826 Genome-wide genotyping array 2018-01-16 29168253 Seielstad M 2017-11-22 Transfusion www.ncbi.nlm.nih.gov/pubmed/29168253 Genomewide association study of HLA alloimmunization in previously pregnant blood donors. Alloimmunization response to pregnancy (HLA class I and II) up to 193 European ancestry alloantibody-positive previously pregnant cases, 753 European ancestry alloantibody-negative previously pregnant controls NA Illumina [9427497] (imputed) 0 pregnancy induced alloimmunization http://www.ebi.ac.uk/efo/EFO_0008462 GCST005154 Genome-wide genotyping array 2018-01-16 29168253 Seielstad M 2017-11-22 Transfusion www.ncbi.nlm.nih.gov/pubmed/29168253 Genomewide association study of HLA alloimmunization in previously pregnant blood donors. Alloimmunization response to pregnancy (HLA class I) up to 247 European ancestry alloantibody-positive previously pregnant cases, 753 European ancestry alloantibody-negative previously pregnant controls NA Illumina [9427497] (imputed) 2 pregnancy induced alloimmunization http://www.ebi.ac.uk/efo/EFO_0008462 GCST005156 Genome-wide genotyping array 2018-01-16 29168253 Seielstad M 2017-11-22 Transfusion www.ncbi.nlm.nih.gov/pubmed/29168253 Genomewide association study of HLA alloimmunization in previously pregnant blood donors. Alloimmunization response to pregnancy (HLA class II) up to 332 European ancestry alloantibody-positive previously pregnant cases, 753 European ancestry alloantibody-negative previously pregnant controls NA Illumina [9427497] (imputed) 0 pregnancy induced alloimmunization http://www.ebi.ac.uk/efo/EFO_0008462 GCST005157 Genome-wide genotyping array 2018-01-16 29168253 Seielstad M 2017-11-22 Transfusion www.ncbi.nlm.nih.gov/pubmed/29168253 Genomewide association study of HLA alloimmunization in previously pregnant blood donors. Alloimmunization response to pregnancy 752 European ancestry alloantibody-positive previously pregnant cases, 753 European ancestry alloantibody-negative previously pregnant controls NA Illumina [9427497] (imputed) 0 pregnancy induced alloimmunization http://www.ebi.ac.uk/efo/EFO_0008462 GCST005155 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist-to-hip ratio adjusted for BMI (joint analysis for main effect and physical activity interaction) 2,518 African American women, 83,707 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 52,993 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 141 BMI-adjusted waist-hip ratio, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0008002 GCST004567 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Body mass index 2,518 African American women, 86,278 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 55,137 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 266 physical activity measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004557 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist circumference adjusted for body mass index 2,518 African American women, 85,730 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 54,792 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 260 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST004562 Genome-wide genotyping array 2017-08-22 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist-to-hip ratio adjusted for body mass index 2,518 African American women, 83,707 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 52,993 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 144 BMI-adjusted waist-hip ratio, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0008002 GCST004576 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Body mass index (physical activity interaction) 2,518 African American women, 86,278 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 55,137 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 2 physical activity measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004568 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist circumference adjusted for BMI (physical activity interaction) 2,518 African American women, 85,730 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 54,792 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 0 BMI-adjusted waist circumference, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0007789, http://www.ebi.ac.uk/efo/EFO_0008002 GCST004561 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist-to-hip ratio adjusted for BMI (physical activity interaction) 2,518 African American women, 83,707 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 52,993 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 0 BMI-adjusted waist-hip ratio, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0008002 GCST004566 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Body mass index (joint analysis main effects and physical activity interaction) 2,518 African American women, 86,278 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 55,137 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 242 physical activity measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004558 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist circumference adjusted for BMI (joint analysis main effects and physical activity interaction) 2,518 African American women, 85,730 European ancestry women, 1,773 Filipino ancestry women, 1,030 Indian ancestry women, 1,457 African American men, 54,792 European ancestry men, 7,648 Indian ancestry men, 5,527 European ancestry individuals 6,244 African American women, 17,531 European ancestry women, 329 African American men, 19,956 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 253 BMI-adjusted waist circumference, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0007789, http://www.ebi.ac.uk/efo/EFO_0008002 GCST004563 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Body mass index in physically active individuals 1,957 African American women, 1,773 Filipino ancestry women, 305 Indian ancestry women, 67,609 European ancestry women, 1,206 African American men, 2,029 Indian ancestry men, 43,399 European ancestry men, at least 4,819 European ancestry individuals 4,807 African American women, 12,347 European ancestry women, 265 African American men, 14,540 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 195 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004559 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Body mass index in physically inactive individuals 561 African American women, 352 Filipino ancestry women, 725 Indian ancestry women, 19,366 European ancestry women, 251 African American men, 4,654 Indian ancestry men, 11,727 European ancestry men, 959 European ancestry individuals 1,437 African American women, 5,184 European ancestry women, 64 African American men, 5,416 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 45 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004560 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist circumference adjusted for BMI in active individuals 1,957 African American women, 1,773 Filipino ancestry women, 305 Indian ancestry women, 67,139 European ancestry women, 1,206 African American men, 2,029 Indian ancestry men, 43,100 European ancestry men, at least 4,819 European ancestry individuals 4,807 African American women, 12,347 European ancestry women, 265 African American men, 14,540 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 235 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST004564 Genome-wide genotyping array 2017-08-18 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist circumference adjusted for BMI in inactive individuals 561 African American women, 352 Filipino ancestry women, 725 Indian ancestry women, 19,288 European ancestry women, 251 African American men, 4,654 Indian ancestry men, 11,681 European ancestry men, 959 European ancestry individuals 1,437 African American women, 5,184 European ancestry women, 64 African American men, 5,416 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 14 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST004565 Genome-wide genotyping array 2017-08-22 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist-to-hip ratio adjusted for BMI in active individuals 1,957 African American women, 1,421 Filipino ancestry women, 305 Indian ancestry women, 65,539 European ancestry women, 1,206 African American men, 2,029 Indian ancestry men, 41,673 European ancestry men, 4,819 European ancestry individuals 4,807 African American women, 12,347 European ancestry women, 265 African American men, 14,540 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 143 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST004578 Genome-wide genotyping array 2017-08-22 28448500 Graff M 2017-04-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28448500 Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. Waist-to-hip ratio adjusted for BMI in inactive individuals 561 African American women, 352 Filipino ancestry women, 725 Indian ancestry women, 18,865 European ancestry women, 251 African American men, 4,654 Indian ancestry men, 11,309 European ancestry men, 959 European ancestry individuals 1,437 African American women, 5,184 European ancestry women, 64 African American men, 5,416 European ancestry men Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 7 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST004577 Genome-wide genotyping array 2018-01-24 29206233 Shendre A 2017-12-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/29206233 Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS). Common carotid intima-media thickness in HIV negative individuals 288 Black non-Hispanic HIV-negative women NA Illumina [1124301] 13 common carotid intimal medial thickness http://www.ebi.ac.uk/efo/EFO_0004860 GCST005182 Genome-wide genotyping array 2018-01-24 29206233 Shendre A 2017-12-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/29206233 Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS). Common carotid intima-media thickness in HIV infection 682 Black non-Hispanic HIV-positive women NA Illumina [1124301] 12 common carotid intimal medial thickness http://www.ebi.ac.uk/efo/EFO_0004860 GCST005184 Genome-wide genotyping array 2018-01-24 29206233 Shendre A 2017-12-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/29206233 Genome-wide admixture and association study of subclinical atherosclerosis in the Women's Interagency HIV Study (WIHS). Common carotid intima-media thickness 682 Black non-Hispanic HIV-positive women, 288 Black non-Hispanic HIV-negative women NA Illumina [1124301] 10 common carotid intimal medial thickness http://www.ebi.ac.uk/efo/EFO_0004860 GCST005183 Genome-wide genotyping array 2018-08-13 27898682 Lotta LA 2016-11-29 PLoS Med www.ncbi.nlm.nih.gov/pubmed/27898682 Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis. Branched-chain amino acid levels (Isoleucine) 16,596 European ancestry individuals NA Affymetrix, Illumina [10500000] (imputed) 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST006077 Genome-wide genotyping array 2018-08-13 27898682 Lotta LA 2016-11-29 PLoS Med www.ncbi.nlm.nih.gov/pubmed/27898682 Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis. Branched-chain amino acid levels (Leucine) 16,596 European ancestry individuals NA Affymetrix, Illumina [10500000] (imputed) 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST006076 Genome-wide genotyping array 2018-08-13 27898682 Lotta LA 2016-11-29 PLoS Med www.ncbi.nlm.nih.gov/pubmed/27898682 Genetic Predisposition to an Impaired Metabolism of the Branched-Chain Amino Acids and Risk of Type 2 Diabetes: A Mendelian Randomisation Analysis. Branched-chain amino acid levels (Valine) 16,596 European ancestry individuals NA Affymetrix, Illumina [10500000] (imputed) 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST006078 Genome-wide genotyping array 2017-09-18 28696415 Maciukiewicz M 2017-07-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/28696415 Genome-wide association studies of placebo and duloxetine response in major depressive disorder. Duloxetine response in major depressive disorder (remitter/non-remitter status) 186 European ancestry individuals NA Illumina [1924595] (imputed) 0 response to duloxetine http://www.ebi.ac.uk/efo/EFO_0008345 GCST004740 Genome-wide genotyping array 2017-09-18 28696415 Maciukiewicz M 2017-07-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/28696415 Genome-wide association studies of placebo and duloxetine response in major depressive disorder. Duloxetine response in major depressive disorder (responder/non-responder status) 186 European ancestry individuals NA Illumina [1924595] (imputed) 0 response to duloxetine http://www.ebi.ac.uk/efo/EFO_0008345 GCST004741 Genome-wide genotyping array 2017-09-18 28696415 Maciukiewicz M 2017-07-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/28696415 Genome-wide association studies of placebo and duloxetine response in major depressive disorder. Placebo response in major depressive disorder (remitter/non-remitter status) 205 European ancestry individuals NA Illumina [1924595] (imputed) 0 response to placebo http://www.ebi.ac.uk/efo/EFO_0008344 GCST004742 Genome-wide genotyping array 2017-09-18 28696415 Maciukiewicz M 2017-07-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/28696415 Genome-wide association studies of placebo and duloxetine response in major depressive disorder. Placebo response in major depressive disorder (responder/non-responder status) 205 European ancestry individuals NA Illumina [1924595] (imputed) 0 response to placebo http://www.ebi.ac.uk/efo/EFO_0008344 GCST004743 Genome-wide genotyping array 2017-09-18 28696415 Maciukiewicz M 2017-07-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/28696415 Genome-wide association studies of placebo and duloxetine response in major depressive disorder. Duloxetine response in major depressive disorder (% change in symptom score) 186 European ancestry individuals NA Illumina [1924595] (imputed) 2 response to duloxetine http://www.ebi.ac.uk/efo/EFO_0008345 GCST004738 Genome-wide genotyping array 2017-09-18 28696415 Maciukiewicz M 2017-07-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/28696415 Genome-wide association studies of placebo and duloxetine response in major depressive disorder. Placebo response in major depressive disorder (% change in symptom score) 205 European ancestry individuals NA Illumina [1924595] (imputed) 2 response to placebo http://www.ebi.ac.uk/efo/EFO_0008344 GCST004739 Genome-wide genotyping array 2018-01-24 27455349 Minster RL 2016-07-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27455349 A thrifty variant in CREBRF strongly influences body mass index in Samoans. Body mass index 3,072 Samoan (founder/genetic isolate) individuals 2,102 Samoan (founder/genetic isolate) individuals Affymetrix [659492] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST005181 Genome-wide genotyping array 2017-09-05 28656603 Na R 2017-06-28 Prostate www.ncbi.nlm.nih.gov/pubmed/28656603 A genetic variant near GATA3 implicated in inherited susceptibility and etiology of benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS). Benign prostatic hyperplasia and/or lower urinary tract symptoms 1,419 European ancestry cases, 498 cases, 1,684 European ancestry controls, 518 controls 485 Finnish ancestry cases, 475 Finnish ancestry controls Illumina [at least 7852412] (imputed) 1 lower urinary tract symptom, benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0008008, http://www.ebi.ac.uk/efo/EFO_0000284 GCST004638 Genome-wide genotyping array 2016-10-04 26482879 Paternoster L 2015-10-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26482879 Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis. Atopic dermatitis 18,900 European ancestry cases, 1,472 Japanese ancestry cases, 422 African American cases, 300 Latino cases, 305 cases, 84,166 European ancestry controls, 7,966 Japanese ancestry controls, 844 African American controls, 1,592 Latino controls, 896 controls 30,588 European ancestry cases, 459 African American cases, 1,012 Chinese ancestry cases, 226,537 European ancestry controls, 729 African American controls, 1,362 Chinese ancestry controls Illumina [15539996] (imputed) 40 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST003184 Genome-wide genotyping array 2017-02-02 27515689 Kerns SL 2016-07-20 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/27515689 Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer. Response to radiotherapy in prostate cancer (toxicity, urinary frequency) 1,409 European ancestry individuals NA NR [~ 38000000] (imputed) 11 response to radiation http://purl.obolibrary.org/obo/GO_0009314 GCST003582 Genome-wide genotyping array 2017-02-02 27515689 Kerns SL 2016-07-20 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/27515689 Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer. Toxicity response to radiotherapy in prostate cancer (decreased urine stream) (time to event) 1,245 European ancestry individuals NA NR [~ 38000000] (imputed) 8 response to radiation http://purl.obolibrary.org/obo/GO_0009314 GCST003581 Genome-wide genotyping array 2017-02-02 27515689 Kerns SL 2016-07-20 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/27515689 Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer. Response to radiotherapy in prostate cancer (overall toxicity) 1,346 European ancestry individuals NA NR [~ 38000000] (imputed) 16 response to radiation http://purl.obolibrary.org/obo/GO_0009314 GCST003583 Genome-wide genotyping array 2017-02-02 27515689 Kerns SL 2016-07-20 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/27515689 Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer. Response to radiotherapy in prostate cancer (toxicity, rectal bleeding) 1,487 European ancestry individuals NA NR [~ 38000000] (imputed) 6 response to radiation http://purl.obolibrary.org/obo/GO_0009314 GCST003584 Genome-wide genotyping array 2016-10-13 26503584 Litchfield K 2015-10-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26503584 Identification of four new susceptibility loci for testicular germ cell tumour. Testicular germ cell tumor 986 European ancestry cases, 4,946 European ancestry controls 4,009 cases, 4,066 controls Illumina [~ 8900000] (imputed) 3 Testicular Germ Cell Tumor http://www.ebi.ac.uk/efo/EFO_1000566 GCST003247 Genome-wide genotyping array 2016-10-13 26503584 Litchfield K 2015-10-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26503584 Identification of four new susceptibility loci for testicular germ cell tumour. Testicular germ cell tumor 986 European ancestry cases, 4,946 European ancestry controls 1,064 European ancestry cases, 4,009 cases, 10,082 European ancestry controls, 4,066 controls Illumina [307291] 3 Testicular Germ Cell Tumor http://www.ebi.ac.uk/efo/EFO_1000566 GCST003246 Genome-wide genotyping array 2018-07-09 29325096 Eriksson AL 2018-01-09 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/29325096 Genetic Determinants of Circulating Estrogen Levels, and Evidence of a Causal Effect of Estradiol on Bone Density in Men. Estradiol levels 11,097 European ancestry men NA Affymetrix, Illumina [~ 2500000] (imputed) 1 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST005828 Genome-wide genotyping array 2018-07-09 29325096 Eriksson AL 2018-01-09 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/29325096 Genetic Determinants of Circulating Estrogen Levels, and Evidence of a Causal Effect of Estradiol on Bone Density in Men. Estrone levels 7,570 European ancestry men NA Affymetrix, Illumina [~ 2500000] (imputed) 4 estrone measurement http://www.ebi.ac.uk/efo/EFO_0007970 GCST005827 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (serum Ig light chain only lambda based profile) 404 cases, controls NA NR [NR] 1 AL amyloidosis, IgG isotype profile measurement http://purl.obolibrary.org/obo/MONDO_0019438, http://www.ebi.ac.uk/efo/EFO_0008366 GCST004804 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (liver involvement) 194 cases, controls NA NR [NR] 1 liver amyloid deposition measurement, AL amyloidosis http://www.ebi.ac.uk/efo/EFO_0008374, http://purl.obolibrary.org/obo/MONDO_0019438 GCST004807 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (heart and kidney involvement) 426 cases, controls NA NR [NR] 1 heart amyloid deposition measurement, AL amyloidosis, kidney amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0008365, http://purl.obolibrary.org/obo/MONDO_0019438, http://www.ebi.ac.uk/efo/EFO_0008371 GCST004806 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light (AL) amyloidosis (serum Ig kappa profile) 85 cases, controls NA NR [NR] 0 AL amyloidosis, IgG isotype profile measurement http://purl.obolibrary.org/obo/MONDO_0019438, http://www.ebi.ac.uk/efo/EFO_0008366 GCST004810 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (serum Ig light chain only lambda/kappa based profile) 535 cases, controls NA NR [NR] 1 AL amyloidosis, IgG isotype profile measurement http://purl.obolibrary.org/obo/MONDO_0019438, http://www.ebi.ac.uk/efo/EFO_0008366 GCST004811 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (serum Ig lambda profile) 345 cases, controls NA NR [NR] 2 AL amyloidosis, IgG isotype profile measurement http://purl.obolibrary.org/obo/MONDO_0019438, http://www.ebi.ac.uk/efo/EFO_0008366 GCST004809 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (heart involvement) 835 cases, controls NA NR [NR] 1 heart amyloid deposition measurement, AL amyloidosis http://www.ebi.ac.uk/efo/EFO_0008365, http://purl.obolibrary.org/obo/MONDO_0019438 GCST004805 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (kidney involvement) 844 cases, controls NA NR [NR] 1 AL amyloidosis, kidney amyloid deposition measurement http://purl.obolibrary.org/obo/MONDO_0019438, http://www.ebi.ac.uk/efo/EFO_0008371 GCST004812 Genome-wide genotyping array 2017-09-28 28679651 Meziane I 2017-07-04 Haematologica www.ncbi.nlm.nih.gov/pubmed/28679651 Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. Immunoglobulin light chain (AL) amyloidosis (serum IgG profile) 447 cases, controls NA NR [NR] 1 AL amyloidosis, IgG isotype profile measurement http://purl.obolibrary.org/obo/MONDO_0019438, http://www.ebi.ac.uk/efo/EFO_0008366 GCST004808 Genome-wide genotyping array 2017-10-24 28892059 Chang D 2017-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28892059 A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci. Parkinson's disease 20,184 European ancestry cases, 397,324 European ancestry controls 5,851 European ancestry cases, 5,866 European ancestry controls Illumina [11933700] (imputed) 55 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST004902 Genome-wide genotyping array 2017-10-08 28886140 Kwon YC 2017-09-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/28886140 Male-specific association of the FCGR2A His167Arg polymorphism with Kawasaki disease. Kawasaki disease 165 East Asian ancestry male cases, 84 East Asian ancestry female cases, 783 East Asian ancestry male controls, 217 East Asian ancestry female controls 705 East Asian ancestry male cases, 507 East Asian ancestry female cases, 1,484 East Asian ancestry male controls, 2,818 East Asian ancestry female controls, 64 male cases, 36 female cases, 180 male controls, 67 male controls Illumina [NR] 1 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST004859 Genome-wide genotyping array 2017-10-24 28898252 Wheeler E 2017-09-12 PLoS Med www.ncbi.nlm.nih.gov/pubmed/28898252 Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. Glycated hemoglobin levels 88,355 European ancestry individuals,18,472 East Asian ancestry individuals, 7,572 South Asian ancestry individuals, 7,564 African American individuals 33,238 European ancestry individuals, 2,366 East Asian ancestry individuals, 1,302 South Asian ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST004903 Genome-wide genotyping array 2019-06-21 28898252 Wheeler E 2017-09-12 PLoS Med www.ncbi.nlm.nih.gov/pubmed/28898252 Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. Glycated hemoglobin levels 7,572 South Asian ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST007951 Genome-wide genotyping array 2019-06-21 28898252 Wheeler E 2017-09-12 PLoS Med www.ncbi.nlm.nih.gov/pubmed/28898252 Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. Glycated hemoglobin levels 88,355 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 52 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST007954 Genome-wide genotyping array 2019-06-21 28898252 Wheeler E 2017-09-12 PLoS Med www.ncbi.nlm.nih.gov/pubmed/28898252 Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. Glycated hemoglobin levels 7,564 African American individuals NA Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 2 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST007952 Genome-wide genotyping array 2019-06-21 28898252 Wheeler E 2017-09-12 PLoS Med www.ncbi.nlm.nih.gov/pubmed/28898252 Impact of common genetic determinants of Hemoglobin A1c on type 2 diabetes risk and diagnosis in ancestrally diverse populations: A transethnic genome-wide meta-analysis. Glycated hemoglobin levels 18,472 East Asian ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 14 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST007953 Genome-wide genotyping array 2017-09-28 28835685 Yamashiro K 2017-08-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28835685 A prospective multicenter study on genome wide associations to ranibizumab treatment outcome for age-related macular degeneration. Response to ranibizumab in age-related macular degeneration (visual acuity) 256 Japanese ancestry treated individuals 205 Japanese ancestry treated individuals Illumina [8480849] (imputed) 0 visual acuity measurement, response to ranibizumab http://www.ebi.ac.uk/efo/EFO_0008385, http://www.ebi.ac.uk/efo/EFO_0008348 GCST004801 Genome-wide genotyping array 2017-09-28 28835685 Yamashiro K 2017-08-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28835685 A prospective multicenter study on genome wide associations to ranibizumab treatment outcome for age-related macular degeneration. Response to ranibizumab in age-related macular degeneration (additional treatment requirement) 256 Japanese ancestry treated individuals 205 Japanese ancestry treated individuals Illumina [8480849] (imputed) 0 response to ranibizumab, treatment outcome measurement http://www.ebi.ac.uk/efo/EFO_0008348, http://www.ebi.ac.uk/efo/EFO_0008383 GCST004803 Genome-wide genotyping array 2017-09-28 28835685 Yamashiro K 2017-08-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28835685 A prospective multicenter study on genome wide associations to ranibizumab treatment outcome for age-related macular degeneration. Response to ranibizumab in age-related macular degeneration (dry maculae) 256 Japanese ancestry treated individuals 205 Japanese ancestry treated individuals Illumina [8480849] (imputed) 0 response to ranibizumab, macula measurement http://www.ebi.ac.uk/efo/EFO_0008348, http://www.ebi.ac.uk/efo/EFO_0008375 GCST004802 Genome-wide genotyping array 2017-03-31 27770449 Tamm R 2016-10-22 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/27770449 Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies. Thiopurine S-methyltransferase activity 844 European ancestry individuals (blood measurement), 123 European ancestry individuals (liver measurement), 245 acute lymphoblastic leukemia cases (blood measurement) NA Illumina [at least 7481872] (imputed) 4 thiopurine methyltransferase activity measurement http://www.ebi.ac.uk/efo/EFO_0007852 GCST003841 Genome-wide genotyping array 2017-09-22 28739976 Wain LV 2017-07-24 Hypertension www.ncbi.nlm.nih.gov/pubmed/28739976 Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Diastolic blood pressure 150,134 European ancestry individuals 87,359 European ancestry individuals, 140,886 European and unknown ancestry individuals Affymetrix, Illumina, Perlegen [7994604] (imputed) 71 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST004777 Genome-wide genotyping array 2017-09-22 28739976 Wain LV 2017-07-24 Hypertension www.ncbi.nlm.nih.gov/pubmed/28739976 Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Systolic blood pressure 150,134 European ancestry individuals 87,359 European ancestry individuals, 140,886 European and unknown ancestry individuals Affymetrix, Illumina, Perlegen [7994604] (imputed) 96 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST004776 Genome-wide genotyping array 2017-09-22 28739976 Wain LV 2017-07-24 Hypertension www.ncbi.nlm.nih.gov/pubmed/28739976 Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney. Pulse pressure 150,134 European ancestry individuals 87,359 European ancestry individuals, 140,886 European and unknown ancestry individuals Affymetrix, Illumina, Perlegen [7994604] (imputed) 46 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST004775 Genome-wide genotyping array 2017-12-11 22885922 Morris AP 2012-09-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22885922 Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. Type 2 diabetes 6,377 European ancestry male cases, 5,794 European ancestry female cases, 22,243 European ancestry male controls, 34,619 European ancestry female controls 12,938 European ancestry male cases, 8,553 European ancestry female cases, 904 Pakistani ancestry male cases, 274 Pakistani ancestry female cases, 30,273 European ancestry male controls, 25,374 European ancestry female controls, 2,088 Pakistani ancestry male controls, 384 Pakistani ancestry female controls Affymetrix, Illumina [up to 2500000] (imputed) 110 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST005047 Genome-wide genotyping array 2017-08-01 28512139 Mack S 2017-05-16 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28512139 A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms. Lipoprotein(a) levels adjusted for apolipoprotein(a) isoforms 13,781 European ancestry individuals NA Affymetrix, Illumina [at least 7600000] (imputed) 28 lipoprotein A measurement, apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0006925, http://www.ebi.ac.uk/efo/EFO_0004614 GCST004399 Genome-wide genotyping array 2017-08-01 28512139 Mack S 2017-05-16 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28512139 A genome-wide association meta-analysis on lipoprotein (a) concentrations adjusted for apolipoprotein (a) isoforms. Lipoprotein (a) levels 13,781 European ancestry individuals NA Affymetrix, Illumina [at least 7600000] (imputed) 44 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST004398 Genome-wide genotyping array 2017-08-03 26853712 Zhang YB 2016-02-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26853712 Genome-wide association study identifies multiple susceptibility loci for craniofacial microsomia. Craniofacial microsomia 330 Chinese ancestry left-side-affected cases, 609 Chinese ancestry right-side-affected cases, 2,012 Chinese ancestry controls 151 Chinese ancestry left-side-affected cases, 292 Chinese ancestry right-side-affected cases, 1,669 Chinese ancestry controls Illumina [792342] 13 hemifacial microsomia http://purl.obolibrary.org/obo/MONDO_0015398 GCST004412 Genome-wide genotyping array 2017-07-10 28425483 Qiu F 2017-04-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28425483 A genome-wide association study identifies six novel risk loci for primary biliary cholangitis. Primary biliary cholangitis 1,122 Han Chinese ancestry cases, 4,036 Han Chinese ancestry controls 907 Han Chinese ancestry cases, 2,127 Han Chinese ancestry controls Illumina [776516] 22 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST004302 Genome-wide genotyping array 2017-03-10 27412988 Tise CG 2016-07-13 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/27412988 From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases. Serum sulfate level 917 Old Order Amish (founder/genetic isolate) individuals NA Affymetrix [NR] 6 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST003723 Genome-wide genotyping array 2018-01-12 29158487 Heckerman D 2017-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29158487 Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Activities of daily living score 286 Sirente (founder/genetic isolate) elderly individuals NA Illumina [at least 547937] (imputed) 0 activities of daily living score measurement http://www.ebi.ac.uk/efo/EFO_0008451 GCST005117 Genome-wide genotyping array 2018-01-12 29158487 Heckerman D 2017-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29158487 Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Short physical performance battery score 286 Sirente (founder/genetic isolate) elderly individuals NA Illumina [at least 547937] (imputed) 0 short physical performance battery score measurement http://www.ebi.ac.uk/efo/EFO_0008454 GCST005121 Genome-wide genotyping array 2018-01-12 29158487 Heckerman D 2017-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29158487 Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Mid-arm muscle circumference 286 Sirente (founder/genetic isolate) elderly individuals NA Illumina [at least 547937] (imputed) 0 mid-arm muscle circumference measurement http://www.ebi.ac.uk/efo/EFO_0008452 GCST005118 Genome-wide genotyping array 2018-01-12 29158487 Heckerman D 2017-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29158487 Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Four meter walk test score 286 Sirente (founder/genetic isolate) elderly individuals 1,055 European ancestry elderly individuals Illumina [at least 547937] (imputed) 0 gait measurement http://www.ebi.ac.uk/efo/EFO_0007680 GCST005120 Genome-wide genotyping array 2018-01-12 29158487 Heckerman D 2017-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29158487 Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Cognitive performance 286 Sirente (founder/genetic isolate) elderly individuals NA Illumina [at least 547937] (imputed) 0 neuropsychological test http://www.ebi.ac.uk/efo/EFO_0003926 GCST005123 Genome-wide genotyping array 2018-01-12 29158487 Heckerman D 2017-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29158487 Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Calf circumference 286 Sirente (founder/genetic isolate) elderly individuals NA Illumina [at least 547937] (imputed) 0 calf circumference measurement http://www.ebi.ac.uk/efo/EFO_0008453 GCST005119 Genome-wide genotyping array 2018-01-12 29158487 Heckerman D 2017-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29158487 Genetic variants associated with physical performance and anthropometry in old age: a genome-wide association study in the ilSIRENTE cohort. Hand grip strength 286 Sirente (founder/genetic isolate) elderly individuals NA Illumina [at least 547937] (imputed) 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST005122 Genome-wide genotyping array 2018-02-13 29374233 Lu AT 2018-01-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29374233 GWAS of epigenetic aging rates in blood reveals a critical role for TERT. Extrinsic epigenetic age acceleration 8,393 European ancestry individuals 1,023 African American individuals, 491 Hispanic individuals Affymetrix, Illumina [~ 7400000] (imputed) 3 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST005288 Genome-wide genotyping array 2018-02-13 29374233 Lu AT 2018-01-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29374233 GWAS of epigenetic aging rates in blood reveals a critical role for TERT. Intrinsic epigenetic age acceleration 8,393 European ancestry individuals 1,023 African American individuals, 491 Hispanic individuals Affymetrix, Illumina [~ 7400000] (imputed) 6 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST005287 Genome-wide genotyping array 2017-05-23 28076899 Taylor KE 2017-01-11 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28076899 Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. Sjögren's syndrome 460 Asian ancestry cases, 1125 Asian ancestry controls NA Illumina [302688] 2 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST004062 Genome-wide genotyping array 2017-05-23 28076899 Taylor KE 2017-01-11 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28076899 Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. Sjögren's syndrome 585 European ancestry cases, up to 51 African ancestry cases, up to 164 Hispanic/Native american cases, up to 570 Asian ancestry cases, up to 59 cases, 1,546 European ancestry controls, 495 African ancestry controls, 237 Hispanic/Native American controls, 306 Asian ancestry controls, 148 controls. NA Illumina [1444884] 10 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST004061 Genome-wide genotyping array 2022-03-23 28076899 Taylor KE 2017-01-11 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28076899 Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. Sjögren's syndrome 585 European ancestry cases, 1,546 European ancestry controls NA Illumina [1444884] 10 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST012796 Genome-wide genotyping array 2017-07-11 28406950 Kim J 2017-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/28406950 Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes. Prevalent type 2 diabetes 911 Korean ancestry prevalent diabetes cases, 7,024 Korean ancestry incident diabetes and non-diabetes controls Affymetrix [352228] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004304 Genome-wide genotyping array 2017-07-11 28406950 Kim J 2017-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/28406950 Interaction of iron status with single nucleotide polymorphisms on incidence of type 2 diabetes. Type 2 diabetes 1,895 Korean ancestry cases, 6,040 Korean ancestry controls NA Affymetrix [352228] 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004305 Genome-wide genotyping array 2017-02-19 26138065 Schneider BP 2015-07-02 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/26138065 Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199. Neuropathy in taxane-treated breast cancer 151 African American cases, 576 European ancestry cases, 62 African American controls, 781 European ancestry controls 52 African American cases, 437 European ancestry cases, 38 African American controls, 352 European ancestry controls Illumina [at least 810891] (imputed) 0 peripheral neuropathy, methylcobalamin deficiency type cblE, response to docetaxel trihydrate http://www.ebi.ac.uk/efo/EFO_0003100, http://purl.obolibrary.org/obo/MONDO_0009354, http://purl.obolibrary.org/obo/GO_1902519 GCST003627 Genome-wide genotyping array 2017-07-27 28461288 Yan Q 2017-05-01 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/28461288 A meta-analysis of genome-wide association studies of asthma in Puerto Ricans. Asthma 1,666 Puerto Rican child cases, 478 Puerto Rican adult cases, 1,505 Puerto Rican child controls, 1,388 Puerto Rican adult controls NA Affymetrix, Illumina [7485508] (imputed) 3 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST004390 Genome-wide genotyping array 2017-09-21 28744025 Woolston AL 2017-07-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28744025 Genetic loci associated with an earlier age at onset in multiplex schizophrenia. Schizophrenia (age at onset) 94 Han Chinese ancestry very early onset cases, 91 Han Chinese ancestry very late onset cases NA Affymetrix [564836] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST004767 Genome-wide genotyping array 2017-10-09 28754779 Rosendahl J 2017-07-28 Gut www.ncbi.nlm.nih.gov/pubmed/28754779 Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. Alcoholic chronic pancreatitis 1,959 European ancestry cases, 1,488 European ancestry alcohol abuse controls, 4,552 European ancestry controls NA Illumina [9389922] (imputed) 156 alcoholic pancreatitis http://www.ebi.ac.uk/efo/EFO_1002013 GCST004860 Genome-wide genotyping array 2017-08-11 28545128 McDaniel LD 2017-05-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28545128 Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma. Sporadic neuroblastoma 2,101 European ancestry child cases, 4,202 European ancestry controls 365 African American child cases, 2,491 African American controls, 427 European ancestry cases, 783 European ancestry controls, 371 cases, 1,122 controls Illumina [7968453] (imputed) 9 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST004510 Genome-wide genotyping array 2017-02-03 27412012 Lamina C 2016-07-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27412012 A genome-wide association meta-analysis on apolipoprotein A-IV concentrations. Apolipoprotein A-IV levels 13,813 European ancestry individuals 2,267 European ancestry individuals Affymetrix, Illumina [at least 7000000] (imputed) 4 apolipoprotein A-IV measurement http://www.ebi.ac.uk/efo/EFO_0007848 GCST003590 Genome-wide genotyping array 2017-02-24 27424798 Chahal HS 2016-07-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27424798 Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma. Cutaneous squamous cell carcinoma 6,579 European ancestry cases, 280,558 European ancestry controls 825 European ancestry cases, 11,518 European ancestry controls Affymetrix, Illumina [at least 560000] (imputed) 13 cutaneous squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_1001927 GCST003655 Genome-wide genotyping array 2018-07-04 29278617 Sucheston-Campbell LE 2018-02-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/29278617 Genome-wide meta-analyses identifies novel taxane-induced peripheral neuropathy-associated loci. Taxane-induced peripheral neuropathy in breast cancer 204 European ancestry cases with ≥ grade 3 neuropathy, 1,919 European ancestry cases with < grade 3 neuropathy, 31 African American cases with ≥ grade 3 neuropathy, 108 African American cases with 552942] (imputed) 2 diffuse large B-cell lymphoma, event free survival time, response to immunochemotherapy http://www.ebi.ac.uk/efo/EFO_0000403, http://www.ebi.ac.uk/efo/EFO_0000482, http://www.ebi.ac.uk/efo/EFO_0007754 GCST003178 Genome-wide genotyping array 2016-09-27 26503763 Song J 2015-10-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26503763 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Subjective response to lithium treatment 1,639 European ancestry bipolar disorder responder cases, 8,899 European ancestry controls NA Affymetrix, Illumina [> 8000000] (imputed) 4 bipolar disorder, response to lithium ion http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/GO_0010226 GCST003158 Genome-wide genotyping array 2016-09-27 26503763 Song J 2015-10-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26503763 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Subjective response to lithium treatment in bipolar disorder 1,639 European ancestry responder cases, 1,059 European ancestry non-responder cases NA NR [> 8000000] (imputed) 4 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST003160 Genome-wide genotyping array 2016-09-27 26503763 Song J 2015-10-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26503763 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Objective response to lithium treatment 323 European ancestry bipolar disorder responder cases, 6,684 European ancestry controls NA Affymetrix, Illumina [> 8000000] (imputed) 4 bipolar disorder, response to lithium ion http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/GO_0010226 GCST003159 Genome-wide genotyping array 2016-09-27 26503763 Song J 2015-10-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26503763 Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder. Objective response to lithium treatment in bipolar disorder 323 European ancestry responder cases, 853 European ancestry non-responder cases NA Affymetrix, Illumina [> 8000000] (imputed) 4 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST003161 Genome-wide genotyping array 2016-09-23 26488411 Matsukura M 2015-10-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/26488411 Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population. Peripheral artery disease 785 Japanese ancestry cases, 3,383 Japanese ancestry controls 2,379 Japanese ancestry cases, 16,752 Japanese ancestry controls Illumina [431666] 4 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST003154 Genome-wide genotyping array 2016-10-06 26491034 Sarzynski MA 2015-10-21 Br J Sports Med www.ncbi.nlm.nih.gov/pubmed/26491034 Genomic and transcriptomic predictors of triglyceride response to regular exercise. Response to exercise (triglyceride level interaction) 478 European ancestry individuals from 99 families NA Illumina [2396589] (imputed) 5 triglyceride change measurement, response to exercise http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0007768 GCST003207 Genome-wide genotyping array 2017-03-29 26503814 Hardin M 2016-10-27 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/26503814 A genome-wide analysis of the response to inhaled β2-agonists in chronic obstructive pulmonary disease. Response to bronchodilator in chronic obstructive pulmonary disease (change in FEV1) 5,766 European ancestry cases, 811 African American cases NA Illumina [NR] (imputed) 57 FEV change measurement, response to bronchodilator http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0097366 GCST003830 Genome-wide genotyping array 2017-10-08 28886342 Ng M 2017-09-07 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28886342 A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis. Dupuytren's disease 3,871 European ancestry cases, 4,686 European ancestry controls 4,041 European and unknown ancestry cases, 8,251 European and unknown ancestry controls Illumina [238825] 28 Dupuytren Contracture http://www.ebi.ac.uk/efo/EFO_0004229 GCST004858 Genome-wide genotyping array 2018-07-23 27018472 Leslie EJ 2016-04-07 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27018472 A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. Cleft palate 38 European ancestry cases, 835 European ancestry controls, 21 Hispanic cases, 626 Hispanic controls, 2 Asian ancestry cases, 161 Asian ancestry controls, 38 Indian ancestry controls, 15 Sub-Saharan African ancestry cases, 2 African American cases, 68 Sub-Saharan African ancestry controls, 5 African American controls, 1 African control, 4 controls 246 European ancestry cases, 1,685 European ancestry controls Illumina [34985077] (imputed) 22 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST005946 Genome-wide genotyping array 2018-07-23 27018472 Leslie EJ 2016-04-07 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27018472 A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. Cleft palate 114 European ancestry case-parent trios, 30 Hispanic case-parent trios, 39 East Asian case-parent trios, 1 South East Asian ancestry case-parent trio, 5 Sub-Saharan African case-parent trios NA Illumina [34985077] (imputed) 4 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST005948 Genome-wide genotyping array 2018-07-23 27018472 Leslie EJ 2016-04-07 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27018472 A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. Cleft palate 38 European ancestry cases, 835 European ancestry controls, 21 Hispanic cases, 626 Hispanic controls, 2 Asian ancestry cases, 161 Asian ancestry controls, 38 Indian ancestry controls, 15 Sub-Saharan African ancestry cases, 2 African American cases, 68 Sub-Saharan African ancestry controls, 5 African American controls, 1 African control, 4 controls, 114 European ancestry case-parent trios, 30 Hispanic case-parent trios, 39 East Asian case-parent trios, 1 South East Asian ancestry case-parent trio, 5 Sub-Saharan African case-parent trios 246 European ancestry cases, 1,685 European ancestry controls Illumina [34985077] (imputed) 13 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST005947 Genome-wide genotyping array 2018-01-30 28934396 Hackinger S 2017-10-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28934396 Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus. Osteoarthritis or lumbar spine bone mineral density 6,694 osteoarthritis cases, 10,968 osteoarthritis controls, 31,800 individuals NA NR [NR] 0 osteoarthritis, spine bone mineral density http://purl.obolibrary.org/obo/MONDO_0005178, http://www.ebi.ac.uk/efo/EFO_0007701 GCST005225 Genome-wide genotyping array 2018-01-30 28934396 Hackinger S 2017-10-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28934396 Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus. Hip osteoarthritis or lumbar spine bone mineral density 3,032 hip osteoarthritis cases, 10,968 osteoarthritis controls, 31,800 individuals NA NR [NR] 0 osteoarthritis, hip, spine bone mineral density http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0007701 GCST005226 Genome-wide genotyping array 2018-01-30 28934396 Hackinger S 2017-10-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28934396 Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus. Knee osteoarthritis or lumbar spine bone mineral density 3,088 knee osteoarthritis cases, 10,968 osteoarthritis controls, 31,800 individuals NA NR [NR] 0 osteoarthritis, knee, spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0007701 GCST005227 Genome-wide genotyping array 2018-01-30 28934396 Hackinger S 2017-10-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28934396 Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus. Osteoarthritis or femoral neck bone mineral density 6,694 osteoarthritis cases, 10,968 osteoarthritis controls, 32,961 individuals NA NR [NR] 0 osteoarthritis, femoral neck bone mineral density http://purl.obolibrary.org/obo/MONDO_0005178, http://www.ebi.ac.uk/efo/EFO_0007785 GCST005228 Genome-wide genotyping array 2018-01-30 28934396 Hackinger S 2017-10-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28934396 Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus. Hip osteoarthritis or femoral neck bone mineral density 3,032 hip osteoarthritis cases, 10,968 osteoarthritis controls, 32,961 individuals NA NR [NR] 0 osteoarthritis, hip, femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0007785 GCST005229 Genome-wide genotyping array 2018-01-30 28934396 Hackinger S 2017-10-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28934396 Evaluation of shared genetic aetiology between osteoarthritis and bone mineral density identifies SMAD3 as a novel osteoarthritis risk locus. Knee osteoarthritis or femoral neck bone mineral density 3,088 knee osteoarthritis cases, 10,968 osteoarthritis controls, 32,961 individuals NA NR [NR] 0 osteoarthritis, knee, femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0007785 GCST005224 Genome-wide genotyping array 2017-11-20 28746715 Smeland OB 2017-07-26 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/28746715 Identification of Genetic Loci Jointly Influencing Schizophrenia Risk and the Cognitive Traits of Verbal-Numerical Reasoning, Reaction Time, and General Cognitive Function. Schizophrenia or general cognitive function (pleiotropy) 34,486 schizophrenia cases, 45,271 controls, 81,837 individuals with cognitive function data NA Affymetrix [NR] 0 schizophrenia, cognitive function measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008354 GCST004975 Genome-wide genotyping array 2017-11-20 28746715 Smeland OB 2017-07-26 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/28746715 Identification of Genetic Loci Jointly Influencing Schizophrenia Risk and the Cognitive Traits of Verbal-Numerical Reasoning, Reaction Time, and General Cognitive Function. Schizophrenia or reaction time (pleiotropy) 34,486 schizophrenia cases, 45,271 controls, 111,483 individuals with reaction time data NA Affymetrix [NR] 0 schizophrenia, reaction time measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008393 GCST004974 Genome-wide genotyping array 2017-11-20 28746715 Smeland OB 2017-07-26 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/28746715 Identification of Genetic Loci Jointly Influencing Schizophrenia Risk and the Cognitive Traits of Verbal-Numerical Reasoning, Reaction Time, and General Cognitive Function. Schizophrenia or verbal-numerical reasoning (pleiotropy) 34,486 schizophrenia cases, 45,271 controls, 36,035 individuals with verbal-numerical reasoning data NA Affymetrix [NR] 0 schizophrenia, verbal-numerical reasoning measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008394 GCST004973 Genome-wide genotyping array 2018-07-02 29325163 Hong J 2018-01-09 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/29325163 Trans-ethnic Evaluation Identifies Novel Low Frequency Loci Associated with 25-Hydroxyvitamin D Concentrations. Serum 25-Hydroxyvitamin D levels 8,541 African American individuals, 3,485 Hispanic American individuals, 16,124 European ancestry individuals NA Affymetrix, Illumina [at least 398246] (imputed) 15 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST005782 Genome-wide genotyping array 2016-10-06 26486471 van Loon J 2015-10-21 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26486471 Genome-wide association studies identify genetic loci for low von Willebrand factor levels. Low vWF levels up to 1,635 European ancestry individuals with low vWF levels, up to 33,286 European ancestry individuals with normal vWF levels NA Affymetrix, Illumina [~ 2600000] (imputed) 10 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST003210 Genome-wide genotyping array 2018-02-01 29317602 Hall LS 2018-01-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29317602 Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank. Major depressive disorder 6,997 European ancestry female cases, 16,172 European ancestry female controls, 3,852 European ancestry male cases, 16,034 European ancestry male controls NA Affymetrix, Illumina [7105178] (imputed) 60 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005231 Genome-wide genotyping array 2018-02-01 29317602 Hall LS 2018-01-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29317602 Genome-wide meta-analyses of stratified depression in Generation Scotland and UK Biobank. Recurrent major depressive disorder 7,345 European ancestry female cases, 32,211 European ancestry female controls NA Affymetrix, Illumina [7105178] (imputed) 23 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005230 Genome-wide genotyping array 2018-03-16 29343764 Jiang X 2018-01-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29343764 Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Vitamin D levels (dietary vitamin D intake interaction) 39,868 European ancestry individuals 2,113 European ancestry individuals Affymetrix, Illumina [at least 1200000] (imputed) 5 vitamin D measurement, vitamin D dietary intake measurement http://www.ebi.ac.uk/efo/EFO_0004631, http://www.ebi.ac.uk/efo/EFO_0008539 GCST005366 Genome-wide genotyping array 2018-03-16 29343764 Jiang X 2018-01-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29343764 Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Vitamin D levels 79,366 European ancestry individuals 42,757 European and unknown ancestry individuals Affymetrix, Illumina [up to 3600000] (imputed) 6 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST005367 Genome-wide genotyping array 2017-07-24 28552477 Ilboudo Y 2017-05-13 Blood Cells Mol Dis www.ncbi.nlm.nih.gov/pubmed/28552477 Genome-wide association study of erythrocyte density in sickle cell disease patients. Mean corpuscular hemoglobin concentration in sickle cell disease 317 cases Illumina [~ 31000000] (imputed) 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST004378 Genome-wide genotyping array 2017-07-24 28552477 Ilboudo Y 2017-05-13 Blood Cells Mol Dis www.ncbi.nlm.nih.gov/pubmed/28552477 Genome-wide association study of erythrocyte density in sickle cell disease patients. Red blood cell density in sickle cell anemia 374 cases NA Illumina [~ 31000000] (imputed) 15 red blood cell density measurement http://www.ebi.ac.uk/efo/EFO_0007978 GCST004379 Genome-wide genotyping array 2017-07-21 28627999 Ikram MA 2017-06-19 J Cereb Blood Flow Metab www.ncbi.nlm.nih.gov/pubmed/28627999 Heritability and genome-wide associations studies of cerebral blood flow in the general population. Cerebral blood flow 4,472 Dutch individuals 1,350 Icelandic individuals Illumina [NR] 1 cerebral blood flow measurement http://www.ebi.ac.uk/efo/EFO_0007980 GCST004376 Genome-wide genotyping array 2017-06-02 28158719 Jain D 2017-02-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28158719 Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. White blood cell count up to 11,809 Hispanic/Latino American individuals up to 7,200 Hispanic/Latino American individuals Illumina [27887661] (imputed) 5 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST004126 Genome-wide genotyping array 2017-06-02 28158719 Jain D 2017-02-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28158719 Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. White blood cell count (basophil) up to 11,809 Hispanic/Latino American individuals up to 7,200 Hispanic/Latino American individuals Illumina [27887661] (imputed) 5 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST004127 Genome-wide genotyping array 2017-06-02 28158719 Jain D 2017-02-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28158719 Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. White blood cell count (eosinophil) up to 11,809 Hispanic/Latino American individuals up to 7,200 Hispanic/Latino American individuals Illumina [27887661] (imputed) 5 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST004135 Genome-wide genotyping array 2017-06-02 28158719 Jain D 2017-02-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28158719 Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. White blood cell count (lymphocyte) up to 11,809 Hispanic/Latino American individuals up to 7,200 Hispanic/Latino American individuals Illumina [27887661] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST004130 Genome-wide genotyping array 2017-06-02 28158719 Jain D 2017-02-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28158719 Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. White blood cell count (monocyte) up to 11,809 Hispanic/Latino American individuals up to 7,200 Hispanic/Latino American individuals Illumina [27887661] (imputed) 9 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST004129 Genome-wide genotyping array 2017-06-02 28158719 Jain D 2017-02-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28158719 Genome-wide association of white blood cell counts in Hispanic/Latino Americans: the Hispanic Community Health Study/Study of Latinos. White blood cell count (neutrophil) up to 11,809 Hispanic/Latino American individuals up to 7,200 Hispanic/Latino American individuals Illumina [27887661] (imputed) 4 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST004128 Genome-wide genotyping array 2018-01-03 29158497 Kadalayil L 2017-11-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29158497 Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young women. Breast cancer (survival) 4,739 European ancestry individuals 1,301 European ancestry individuals, 2 South African individuals Illumina [5848861] (imputed) 0 survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST005106 Genome-wide genotyping array 2017-08-21 28502801 Law MH 2017-05-11 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/28502801 Genome-Wide Association Shows that Pigmentation Genes Play a Role in Skin Aging. Skin aging (microtopography measurement) 5,087 individuals NA Illumina [at least 233546] (imputed) 14 skin aging measurement http://www.ebi.ac.uk/efo/EFO_0008006 GCST004574 Genome-wide genotyping array 2017-10-09 28199695 Jones AV 2017-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28199695 GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci. Itch intensity from mosquito bite 84,724 European ancestry individuals NA Illumina [13520550] (imputed) 98 mosquito bite reaction itch intensity measurement http://www.ebi.ac.uk/efo/EFO_0008377 GCST004861 Genome-wide genotyping array 2017-10-09 28199695 Jones AV 2017-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28199695 GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci. Itch intensity from mosquito bite adjusted by bite size 41,355 European ancestry men and 43,369 European ancestry women NA Illumina [13520550] (imputed) 240 mosquito bite reaction itch intensity measurement, mosquito bite reaction size measurement http://www.ebi.ac.uk/efo/EFO_0008377, http://www.ebi.ac.uk/efo/EFO_0008378 GCST004862 Genome-wide genotyping array 2017-10-09 28199695 Jones AV 2017-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28199695 GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci. Mosquito bite size 84,724 European ancestry individuals NA Illumina [13520550] (imputed) 147 mosquito bite reaction size measurement http://www.ebi.ac.uk/efo/EFO_0008378 GCST004863 Genome-wide genotyping array 2017-10-09 28199695 Jones AV 2017-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28199695 GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci. Perceived unattractiveness to mosquitoes 16,576 European ancestry individuals NA Illumina [7433384] (imputed) 45 perceived unattractiveness to mosquitos measurement http://www.ebi.ac.uk/efo/EFO_0008380 GCST004864 Genome-wide genotyping array 2017-10-09 28199695 Jones AV 2017-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28199695 GWAS of self-reported mosquito bite size, itch intensity and attractiveness to mosquitoes implicates immune-related predisposition loci. Itch intensity from mosquito bite adjusted by bite size 69,057 European ancestry individuals without immune related conditions NA Illumina [13519193] (imputed) 96 mosquito bite reaction itch intensity measurement, mosquito bite reaction size measurement http://www.ebi.ac.uk/efo/EFO_0008377, http://www.ebi.ac.uk/efo/EFO_0008378 GCST004865 Genome-wide genotyping array 2018-04-25 23143594 Tsoi LC 2012-12-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23143594 Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Psoriasis 10,588 European ancestry cases, 22,806 European ancestry controls NA Illumina [111236] (imputed) 41 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST005527 Targeted genotyping array [ImmunoChip] 2018-01-30 29237677 Salo PP 2017-12-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29237677 Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population. B-type natriuretic peptide to N-terminal pro B-type natriuretic peptide ratio 4,932 Finnish ancestry individuals 1,373 Finnish ancestry individuals Illumina [7358451] (imputed) 4 B-type natriuretic peptide to N-terminal pro B-type natriuretic peptide ratio http://www.ebi.ac.uk/efo/EFO_0008469 GCST005208 Genome-wide genotyping array 2018-01-30 29237677 Salo PP 2017-12-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29237677 Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population. Midregional pro atrial natriuretic peptide levels 4,932 Finnish ancestry individuals 1,373 Finnish ancestry individuals Illumina [7358451] (imputed) 2 midregional pro atrial natriuretic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008468 GCST005207 Genome-wide genotyping array 2018-01-30 29237677 Salo PP 2017-12-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29237677 Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population. N-terminal pro B-type natriuretic peptide levels 4,932 Finnish ancestry individuals 1,373 Finnish ancestry individuals Illumina [7358451] (imputed) 2 NT-proBNP measurement http://www.ebi.ac.uk/efo/EFO_0004745 GCST005205 Genome-wide genotyping array 2018-01-30 29237677 Salo PP 2017-12-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29237677 Genome-Wide Association Study Implicates Atrial Natriuretic Peptide Rather Than B-Type Natriuretic Peptide in the Regulation of Blood Pressure in the General Population. B-type natriuretic peptide levels 4,932 Finnish ancestry individuals 1,373 Finnish ancestry individuals Illumina [7358451] (imputed) 1 BNP measurement http://www.ebi.ac.uk/efo/EFO_0006920 GCST005206 Genome-wide genotyping array 2017-10-31 28979897 Zeller T 2017-09-20 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/28979897 Genome-Wide Association Analysis for Severity of Coronary Artery Disease Using the Gensini Scoring System. Coronary artery disease severity measurement 4,931 European ancestry individuals 2,283 European ancestry individuals Affymetrix [2500000] (imputed) 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST004918 Genome-wide genotyping array 2017-11-17 28979981 Tielbeek JJ 2017-10-04 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/28979981 Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior. Antisocial behavior 7,054 European ancestry men, 7,926 European ancestry women Affymetrix, Illumina [7392849] (imputed) 0 antisocial behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007052 GCST004954 Genome-wide genotyping array 2018-11-02 28979981 Tielbeek JJ 2017-10-04 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/28979981 Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior. Antisocial behavior 7,926 European ancestry women Affymetrix, Illumina [7392849] (imputed) 0 antisocial behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007052 GCST006490 Genome-wide genotyping array 2018-11-02 28979981 Tielbeek JJ 2017-10-04 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/28979981 Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior. Antisocial behavior 7,054 European ancestry men Affymetrix, Illumina [7392849] (imputed) 0 antisocial behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007052 GCST006489 Genome-wide genotyping array 2017-08-31 28604728 Litchfield K 2017-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28604728 Identification of 19 new risk loci and potential regulatory mechanisms influencing susceptibility to testicular germ cell tumor. Testicular germ cell tumor 5,518 European ancestry cases, 19,055 European ancestry controls 1,801 European ancestry cases, 4,027 European ancestry controls Illumina [at least 371504] (imputed) 43 Testicular Germ Cell Tumor http://www.ebi.ac.uk/efo/EFO_1000566 GCST004635 Genome-wide genotyping array 2017-07-17 28429243 Dudenkov TM 2017-04-20 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/28429243 SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway. Estrone conjugates/estrone ratio in resected early stage estrogen-receptor positive breast cancer 707 European ancestry postmenopausal cases, 52 African ancestry postmenopausal cases, 15 Asian ancestry postmenopausal cases NA Illumina [8203257] (imputed) 1 estrone conjugate measurement, estrone measurement http://www.ebi.ac.uk/efo/EFO_0007971, http://www.ebi.ac.uk/efo/EFO_0007970 GCST004360 Genome-wide genotyping array 2017-07-17 28429243 Dudenkov TM 2017-04-20 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/28429243 SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway. Estrone/androstenedione ratio in resected early stage-receptor positive breast cancer 707 European ancestry postmenopausal cases, 52 African ancestry postmenopausal cases, 15 Asian ancestry postmenopausal cases NA Illumina [8203257] (imputed) 14 androstenedione measurement, estrone measurement http://www.ebi.ac.uk/efo/EFO_0007972, http://www.ebi.ac.uk/efo/EFO_0007970 GCST004361 Genome-wide genotyping array 2017-07-17 28429243 Dudenkov TM 2017-04-20 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/28429243 SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway. Plasma estrone levels in resected estrogen-receptor positive breast cancer 707 European ancestry postmenopausal cases, 52 African ancestry postmenopausal cases, 15 Asian ancestry postmenopausal cases NA Illumina [8203257] (imputed) 2 estrone measurement http://www.ebi.ac.uk/efo/EFO_0007970 GCST004362 Genome-wide genotyping array 2017-07-17 28429243 Dudenkov TM 2017-04-20 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/28429243 SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway. Plasma androstenedione levels in resected early stage-receptor positive breast cancer 707 European ancestry postmenopausal cases, 52 African ancestry postmenopausal cases, 15 Asian ancestry postmenopausal cases NA Illumina [8203257] (imputed) 5 androstenedione measurement http://www.ebi.ac.uk/efo/EFO_0007972 GCST004363 Genome-wide genotyping array 2017-07-17 28429243 Dudenkov TM 2017-04-20 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/28429243 SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway. Plasma estrone conjugates levels in resected early stage estrogen-receptor positive breast cancer 707 European ancestry postmenopausal cases, 52 African ancestry postmenopausal cases, 15 Asian ancestry postmenopausal cases NA Illumina [8203257] (imputed) 2 estrone conjugate measurement http://www.ebi.ac.uk/efo/EFO_0007971 GCST004359 Genome-wide genotyping array 2017-08-14 28430825 Ng MCY 2017-04-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28430825 Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium. Waist-to-hip ratio adjusted for body mass index 4,783 African American men, 15,601 African American women 981 African American men, 1,730 African American women, 104,079 European ancestry men, 116,742 European ancestry women Affymetrix, Illumina [20502658] (imputed) 13 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST004518 Genome-wide genotyping array 2017-08-14 28430825 Ng MCY 2017-04-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28430825 Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium. Body mass index (adult) 16,559 African ancestry men, 26,193 African ancestry women 2,458 African ancestry men, 7,685 African ancestry women, 152,893 European ancestry men, 171,977 European ancestry women Affymetrix, Illumina [17972087] (imputed) 32 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004519 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Visceral adipose tissue/subcutaneous adipose tissue ratio 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American individuals Affymetrix, Illumina [2473256] (imputed) 0 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST003162 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Subcutaneous adipose tissue adjusted for BMI 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American individuals Affymetrix, Illumina [2473256] (imputed) 0 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST003165 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Visceral adipose tissue adjusted for BMI 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American individuals Affymetrix, Illumina [2473256] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST003167 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Total adipose tissue adjusted for BMI 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American individuals Affymetrix, Illumina [2473256] (imputed) 0 adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004764 GCST003169 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Visceral adipose tissue/subcutaneous adipose tissue ratio adjusted for BMI 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American individuals Affymetrix, Illumina [2473256] (imputed) 0 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST003163 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Subcutaneous adipose tissue 1,152 European ancestry males, 1,361 European ancestry females NA Affymetrix, Illumina [2473256] (imputed) 9 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST003170 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Visceral adipose tissue 1,152 European ancestry males, 1,361 European ancestry females NA Affymetrix, Illumina [2473256] (imputed) 4 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST003171 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Visceral adipose tissue adjusted for BMI 1,152 European ancestry males, 1,361 European ancestry females NA Affymetrix, Illumina [2473256] (imputed) 1 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST003172 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Visceral adipose tissue/subcutaneous adipose tissue ratio 1,152 European ancestry males, 1,361 European ancestry females NA Affymetrix, Illumina [2473256] (imputed) 3 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST003173 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Visceral adipose tissue 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American individuals Affymetrix, Illumina [2473256] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST003166 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Total adipose tissue 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American individuals Affymetrix, Illumina [2473256] (imputed) 0 adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004764 GCST003168 Genome-wide genotyping array 2016-09-27 26480920 Sung YJ 2015-10-20 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26480920 Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat. Subcutaneous adipose tissue 2,513 European ancestry individuals 2,171 European ancestry individuals, 772 African American ancestry individuals Affymetrix, Illumina [2473256] (imputed) 0 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST003164 Genome-wide genotyping array 2018-04-26 26051272 Fischer A 2015-09-15 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26051272 Identification of Immune-Relevant Factors Conferring Sarcoidosis Genetic Risk. Sarcoidosis 1,726 European ancestry cases, 5,482 European ancestry controls 1,912 European ancestry cases, 5,938 European ancestry controls, 781 African American cases, 876 African American controls Illumina [128705] 9 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST005538 Targeted genotyping array [ImmunoChip] 2017-07-13 28537254 Tsoi LC 2017-05-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28537254 Large scale meta-analysis characterizes genetic architecture for common psoriasis associated variants. Psoriasis Up to 11,988 European ancestry cases, up to 275,335 European ancestry controls 7,044 European ancestry cases, 11,434 European ancestry controls Illumina, Perlegen [9113515] (imputed) 61 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST004346 Genome-wide genotyping array 2017-08-16 28476931 Piaggi P 2017-05-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/28476931 A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians. Energy expenditure (24h) 419 Pima Indian ancestry individuals NA Affymetrix [491265] 9 energy expenditure measurement http://www.ebi.ac.uk/efo/EFO_0008005 GCST004524 Genome-wide genotyping array 2017-08-16 28476931 Piaggi P 2017-05-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/28476931 A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians. Resting metabolic rate 509 Pima Indian ancestry individuals NA Affymetrix [491265] 10 resting metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0008004 GCST004523 Genome-wide genotyping array 2017-07-14 28460022 Lee JY 2017-04-27 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/28460022 Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci. Early onset atrial fibrillation 672 Korean ancestry cases, 3,700 Korean ancestry controls 200 Korean ancestry cases, 1,812 Korean ancestry controls Affymetrix [642422] 6 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004352 Genome-wide genotyping array 2017-08-03 28447399 Jia P 2017-04-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28447399 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. Neurocognitive impairment in HIV-1 infection (continuous) 490 African American individuals, 443 European ancestry individuals, 99 Hispanic individuals, 17 individuals NA Affymetrix [NR] 6 cognitive impairment measurement http://www.ebi.ac.uk/efo/EFO_0007998 GCST004406 Genome-wide genotyping array 2017-08-03 28447399 Jia P 2017-04-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28447399 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. HIV-associated neurocognitive disorder (mild neurocognitive disorder or asymptomatic neurocognitive impairment) 155 African American asymptomatic neurocognitive impairment cases, 150 European ancestry asymptomatic neurocognitive impairment cases, 49 Hispanic asymptomatic neurocognitive impairment cases, 5 asymptomatic neurocognitive impairment cases, 30 African American mild neurocognitive disorder cases, 45 European ancestry mild neurocognitive disorder cases, 17 Hispanic mild neurocognitive disorder cases, 297 African American controls, 230 European ancestry controls, 29 Hispanic controls, 11 controls NA Affymetrix [NR] 4 HIV-associated neurocognitive disorder, mild neurocognitive disorder, asymptomatic neurocognitive impairment http://www.ebi.ac.uk/efo/EFO_0007948, http://www.ebi.ac.uk/efo/EFO_0007982, http://www.ebi.ac.uk/efo/EFO_0007983 GCST004411 Genome-wide genotyping array 2017-08-03 28447399 Jia P 2017-04-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28447399 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. HIV-associated neurocognitive disorder (mild neurocognitive disorder) 30 African American cases, 45 European ancestry cases, 17 Hispanic cases, 297 African American controls, 230 European ancestry controls, 29 Hispanic controls, 11 controls NA Affymetrix [NR] 3 HIV-associated neurocognitive disorder, mild neurocognitive disorder http://www.ebi.ac.uk/efo/EFO_0007948, http://www.ebi.ac.uk/efo/EFO_0007982 GCST004408 Genome-wide genotyping array 2017-08-03 28447399 Jia P 2017-04-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28447399 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. HIV-associated neurocognitive disorder 192 African American cases, 213 European ancestry cases, 70 Hispanic cases, 6 unknown ancestry cases, 297 African American controls, 230 European ancestry controls, 29 Hispanic controls, 11 controls NA Affymetrix [NR] 2 HIV-associated neurocognitive disorder http://www.ebi.ac.uk/efo/EFO_0007948 GCST004409 Genome-wide genotyping array 2017-08-03 28447399 Jia P 2017-04-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28447399 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. Neurocognitive impairment in HIV-1 infection (dichotomous) 140 African American cases, 167 European ancestry cases, 53 Hispanic cases, 6 cases, 350 African American controls, 276 European ancestry controls, 46 Hispanic controls, 11 controls NA Affymetrix [NR] 9 cognitive impairment measurement http://www.ebi.ac.uk/efo/EFO_0007998 GCST004407 Genome-wide genotyping array 2017-08-03 28447399 Jia P 2017-04-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28447399 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study. HIV-associated neurocognitive disorder (asymptomatic neurocogntive impairment) 155 African American cases, 150 European ancestry cases, 49 Hispanic cases, 5 cases, 297 African American controls, 230 European ancestry controls, 29 Hispanic controls, 11 controls NA Affymetrix [NR] 3 HIV-associated neurocognitive disorder, asymptomatic neurocognitive impairment http://www.ebi.ac.uk/efo/EFO_0007948, http://www.ebi.ac.uk/efo/EFO_0007983 GCST004410 Genome-wide genotyping array 2017-07-10 28449029 Munz M 2017-04-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28449029 A genome-wide association study identifies nucleotide variants at SIGLEC5 and DEFA1A3 as risk loci for periodontitis. Aggressive periodontitis 851 European ancestry cases, 6,836 European ancestry controls 223 cases, up to 564 controls Illumina [at least 5870152] (imputed) 5 aggressive periodontitis http://www.ebi.ac.uk/efo/EFO_0006342 GCST004303 Genome-wide genotyping array 2018-01-12 29151059 Delgado DA 2017-11-18 J Med Genet www.ncbi.nlm.nih.gov/pubmed/29151059 Genome-wide association study of telomere length among South Asians identifies a second RTEL1 association signal. Telomere length 5,075 Bangladeshi ancestry individuals NA Illumina [~ 6300000] (imputed) 7 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST005143 Genome-wide genotyping array 2018-08-13 26148204 Wanga V 2015-09-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/26148204 Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 6-month creatinine clearance change response to tenofovir treatment in HIV infection (concomitant antiretroviral treatment interaction) 243 European American ancestry tenofovir-treated cases, 149 African American tenofovir-treated cases, 100 Hispanic American tenofovir-treated cases, 9 unknown ancestry tenofovir-treated cases, 243 European American ancestry abacavir-treated cases, 189 African American abacavir-treated cases, 102 Hispanic American abacavir-treated cases, 14 unknown ancestry abacavir-treated cases. NA Illumina [~ 5140000] (imputed) 0 response to tenofovir, creatinine clearance measurement http://www.ebi.ac.uk/efo/EFO_0009279, http://www.ebi.ac.uk/efo/EFO_0007934 GCST006070 Genome-wide genotyping array 2018-08-13 26148204 Wanga V 2015-09-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/26148204 Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. Tenofovir clearance in HIV infection (concomitant antiretroviral treatment interaction) 243 European American ancestry cases, 149 African American cases, 100 Hispanic American cases, 9 unknown ancestry cases NA Illumina [~ 5190000] (imputed) 0 response to tenofovir http://www.ebi.ac.uk/efo/EFO_0009279 GCST006071 Genome-wide genotyping array 2018-08-13 26148204 Wanga V 2015-09-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/26148204 Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. Time-dependent creatinine clearance change response to tenofovir treatment in HIV infection (time and treatment arm interaction) 243 European American ancestry tenofovir-treated cases, 149 African American tenofovir-treated cases, 100 Hispanic American tenofovir-treated cases, 9 unknown ancestry tenofovir-treated cases, 243 European American ancestry abacavir-treated cases, 189 African American abacavir-treated cases, 102 Hispanic American abacavir-treated cases, 14 unknown ancestry abacavir-treated cases. NA Illumina [~ 5140000] (imputed) 98 response to tenofovir, creatinine clearance measurement http://www.ebi.ac.uk/efo/EFO_0009279, http://www.ebi.ac.uk/efo/EFO_0007934 GCST006069 Genome-wide genotyping array 2018-08-13 26148204 Wanga V 2015-09-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/26148204 Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. 6-month creatinine clearance change response to tenofovir treatment in HIV infection (treatment arm interaction) 243 European American ancestry tenofovir-treated cases, 149 African American tenofovir-treated cases, 100 Hispanic American tenofovir-treated cases, 9 unknown ancestry tenofovir-treated cases, 243 European American ancestry abacavir-treated cases, 189 African American abacavir-treated cases, 102 Hispanic American abacavir-treated cases, 14 unknown ancestry abacavir-treated cases. NA Illumina [~ 5140000] (imputed) 106 response to tenofovir, creatinine clearance measurement http://www.ebi.ac.uk/efo/EFO_0009279, http://www.ebi.ac.uk/efo/EFO_0007934 GCST006072 Genome-wide genotyping array 2018-08-13 26148204 Wanga V 2015-09-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/26148204 Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. Tenofovir clearance in HIV infection 243 European ancestry cases, 149 African American cases, 100 Hispanic American cases, 9 unknown ancestry cases NA Illumina [~ 5190000] (imputed) 81 response to tenofovir http://www.ebi.ac.uk/efo/EFO_0009279 GCST006073 Genome-wide genotyping array 2018-08-13 26148204 Wanga V 2015-09-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/26148204 Genomewide association study of tenofovir pharmacokinetics and creatinine clearance in AIDS Clinical Trials Group protocol A5202. Bilirubin levels in tenofovir-treated HIV infection 243 European ancestry cases, 149 African American cases, 100 Hispanic American cases, 9 unknown ancestry cases NA Illumina [~ 5190000] (imputed) 20 bilirubin measurement, response to tenofovir http://www.ebi.ac.uk/efo/EFO_0004570, http://www.ebi.ac.uk/efo/EFO_0009279 GCST006074 Genome-wide genotyping array 2019-02-13 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. Low density lipoprotein cholesterol levels 265,204 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 23 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST007131 Genome-wide genotyping array 2019-02-14 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. High density lipoprotein cholesterol levels 76,627 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 797 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007140 Genome-wide genotyping array 2019-02-14 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. Low density lipoprotein cholesterol levels 76,627 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 699 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST007141 Genome-wide genotyping array 2019-02-13 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. High density lipoprotein cholesterol levels 265,204 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 23 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007132 Genome-wide genotyping array 2019-02-13 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. Triglycerides 265,204 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 22 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST007133 Genome-wide genotyping array 2019-02-13 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. Total cholesterol levels 265,204 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 24 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST007134 Genome-wide genotyping array 2019-02-14 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. Triglycerides 76,627 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 696 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST007142 Genome-wide genotyping array 2019-02-14 29507422 Hoffmann TJ 2018-03-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29507422 A large electronic-health-record-based genome-wide study of serum lipids. Total cholesterol levels 76,627 European ancestry individuals, 7,795 Hispanic individuals, 6,855 East Asian ancestry individuals, 2,958 African American individuals, 439 South Asian ancestry individuals NA Affymetrix [at least 7091467] (imputed) 805 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST007143 Genome-wide genotyping array 2017-07-18 28530673 Sniekers S 2017-05-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28530673 Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence. Intelligence up to 58,799 European ancestry adults, up to 19,509 European ancestry children NA Affymetrix, Illumina [12104294] (imputed) 36 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST004364 Genome-wide genotyping array 2017-07-14 28542097 Wells QS 2017-05-24 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/28542097 Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults. Left ventricular function change in anthracycline treatment 337 European ancestry individuals, 30 African American individuals, 1 Asian individual, 4 Latino individuals, 13 individuals 152 European ancestry individuals, 23 African American individuals, 3 Asian individuals, 3 individuals Illumina [4429986] (imputed) 1 left ventricular function, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004295, http://www.ebi.ac.uk/efo/EFO_0005257 GCST004353 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. BMI (smoking interaction) 98,173 European ancestry women, 64,373 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 2 smoking behavior, body mass index http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004496 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist circumference adjusted for BMI (adjusted for smoking behaviour) 97,400 European ancestry women, 63,892 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 140 smoking behavior, BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0007789 GCST004500 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist-to-hip ratio adjusted for BMI (adjusted for smoking behaviour) 95,362 European ancestry women, 62,085 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 116 smoking behavior, BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0007788 GCST004505 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist-to-hip ratio adjusted for BMI (smoking interaction) 95,362 European ancestry women, 62,085 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 2 smoking behavior, BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0007788 GCST004506 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist circumference adjusted for BMI (smoking interaction) 97,400 European ancestry women, 63,892 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 2 smoking behavior, BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0007789 GCST004502 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist circumference adjusted for BMI (joint analysis main effects and smoking interaction) 97,400 European ancestry women, 63,892 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 135 smoking behavior, BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0007789 GCST004501 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist-to-hip ratio adjusted for BMI (joint analysis main effects and smoking interaction) 95,362 European ancestry women, 62,085 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 45 smoking behavior, BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0007788 GCST004507 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. BMI (adjusted for smoking behaviour) 98,173 European ancestry women, 64,373 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 145 smoking behavior, body mass index http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004495 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Body mass index (joint analysis main effects and smoking interaction) 98,173 European ancestry women, 64,373 European ancestry men, 5,829 European ancestry individuals, 10,500 African American/Afro-Caribbean ancestry women, 2,706 African American/Afro-Caribbean ancestry men, 1,030 Indian Asian ancestry women, 7,648 Indian Asian ancestry men, 1,793 Filipino ancestry women, 2,944 Hispanic/Latino ancestry women, 1,764 Hispanic/Latino ancestry men 21,496 European ancestry women, 24,385 European ancestry men, 118,364 European ancestry individuals, 2,326 African American/Afro-Caribbean ancestry women, 855 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 140 smoking behavior, body mass index http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004497 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist circumference adjusted for BMI in non-smokers 77,113 European ancestry women, 47,319 European ancestry men, 4,856 European ancestry individuals, 8,799 African American/Afro-Caribbean ancestry women, 1,803 African American/Afro-Caribbean ancestry men, 1,020 Indian Asian ancestry women, 6,691 Indian Asian ancestry men, 1,526 Filipino ancestry women, 2,469 Hispanic/Latino ancestry women, 1,318 Hispanic/Latino ancestry men 16,011 European ancestry women, 17,912 European ancestry men, 105,218 European ancestry individuals, 2,073 African American/Afro-Caribbean ancestry women, 647 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 108 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST004504 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist-to-hip ratio adjusted for BMI in smokers 18,972 European ancestry women, 16,109 European ancestry men, 973 European ancestry individuals, 1,701 African American/Afro-Caribbean ancestry women, 903 African American/Afro-Caribbean ancestry men, 10 Indian Asian ancestry women, 957 Indian Asian ancestry men, 267 Filipino ancestry women, 475 Hispanic/Latino ancestry women, 446 Hispanic/Latino ancestry men 5,485 European ancestry women, 6,471 European ancestry men, 13,416 European ancestry individuals, 253 African American/Afro-Caribbean ancestry women, 208 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 1 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST004509 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. BMI in non-smokers 77,279 European ancestry women, 47,280 European ancestry men, 4,856 European ancestry individuals, 8,799 African American/Afro-Caribbean ancestry women, 1,803 African American/Afro-Caribbean ancestry men, 1,020 Indian Asian ancestry women, 6,691 Indian Asian ancestry men, 1,526 Filipino ancestry women, 2,469 Hispanic/Latino ancestry women, 1,318 Hispanic/Latino ancestry men 16,011 European ancestry women, 17,912 European ancestry men, 105,218 European ancestry individuals, 2,073 African American/Afro-Caribbean ancestry women, 647 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 105 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004499 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist circumference adjusted for BMI in smokers 19,276 European ancestry women, 16,408 European ancestry men, 973 European ancestry individuals, 1,701 African American/Afro-Caribbean ancestry women, 903 African American/Afro-Caribbean ancestry men, 10 Indian Asian ancestry women, 957 Indian Asian ancestry men, 267 Filipino ancestry women, 475 Hispanic/Latino ancestry women, 446 Hispanic/Latino ancestry men 5,485 European ancestry women, 6,471 European ancestry men, 13,416 European ancestry individuals, 253 African American/Afro-Caribbean ancestry women, 208 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 15 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST004503 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. BMI in smokers 19,883 European ancestry women, up to 16,928 European ancestry men, up to 973 European ancestry individuals, 1,701 African American/Afro-Caribbean ancestry women, 903 African American/Afro-Caribbean ancestry men, 10 Indian Asian ancestry women, 957 Indian Asian ancestry men, 267 Filipino ancestry women, 475 Hispanic/Latino ancestry women, 446 Hispanic/Latino ancestry men 5,485 European ancestry women, 6,471 European ancestry men, 13,416 European ancestry individuals, 253 African American/Afro-Caribbean ancestry women, 208 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 30 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004498 Genome-wide genotyping array 2017-08-10 28443625 Justice AE 2017-04-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28443625 Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits. Waist-to-hip ratio adjusted for BMI in non-smokers 75,379 European ancestry women, 45,811 European ancestry men, 4,856 European ancestry individuals, 8,799 African American/Afro-Caribbean ancestry women, 1,803 African American/Afro-Caribbean ancestry men, 1,020 Indian Asian ancestry women, 6,691 Indian Asian ancestry men, 1,526 Filipino ancestry women, 2,469 Hispanic/Latino ancestry women, 1,318 Hispanic/Latino ancestry men 16,011 European ancestry women, 17,912 European ancestry men, 105,218 European ancestry individuals, 2,073 African American/Afro-Caribbean ancestry women, 647 African American/Afro-Caribbean ancestry men Affymetrix, Illumina, Perlegen [up to 2800000] (imputed) 46 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST004508 Genome-wide genotyping array 2017-10-09 19838195 Gateva V 2009-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19838195 A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus. Systemic lupus erythematosus 1,310 European ancestry cases, 7,859 European ancestry controls 1,963 European ancestry cases, 4,329 European ancestry controls Illumina [~ 2100000] (imputed) 41 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST004867 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (hypomanic personality scale) 3,967 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 6 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004678 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (perceptual aberration scale) 4,057 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 3 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004685 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (revised physical anhedonia scale) 3,988 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 1 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004680 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (revised social anhedonia scale) 4,025 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 2 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004686 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (hypomanic personality scale and perceptual aberration scale) 3,824 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 4 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004679 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (schizoidia scale) 4,191 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 0 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004687 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (hypomanic personality scale and revised physical anhedonia scale) 3,787 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 6 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004681 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (hypomanic personality scale and revised social anhedonia scale) 3,837 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 5 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004682 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (perceptual aberration scale and revised physical anhedonia scale) 3,812 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 1 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004688 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (perceptual aberration scale and revised social anhedonia scale) 3,868 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 2 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004683 Genome-wide genotyping array 2017-09-10 28525603 Ortega-Alonso A 2017-05-19 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/28525603 Genome-Wide Association Study of Psychosis Proneness in the Finnish Population. Psychosis proneness (revised physical anhedonia scale and revised social anhedonia scale) 3,820 Finnish ancestry individuals NA Illumina [~ 9600000] (imputed) 2 psychosis predisposition measurement http://www.ebi.ac.uk/efo/EFO_0008337 GCST004684 Genome-wide genotyping array 2017-10-23 28877031 Zhang G 2017-09-07 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/28877031 Genetic Associations with Gestational Duration and Spontaneous Preterm Birth. Preterm birth (maternal effect) 3,331 European ancestry preterm birth mothers, 40,236 European ancestry term birth mothers 2,565 European ancestry preterm birth mothers, 6,034 European ancestry term birth mothers Illumina [15635593] (imputed) 5 premature birth, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0003917, http://www.ebi.ac.uk/efo/EFO_0005939 GCST004898 Genome-wide genotyping array 2017-10-23 28877031 Zhang G 2017-09-07 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/28877031 Genetic Associations with Gestational Duration and Spontaneous Preterm Birth. Gestational age at birth (maternal effect) 43,568 European ancestry mothers 8,643 European ancestry mothers Illumina [15635593] (imputed) 11 gestational age, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0005939 GCST004899 Genome-wide genotyping array 2017-04-07 27816938 Tanaka T 2016-11-05 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/27816938 Genome-wide Association Study of Parental Life Span. Parental longevity (at least one long-lived parent) 1,140 European American individuals with at least one long-lived parent, 3,894 European American individuals, 137 African American individuals with at least one long-lived parent, 545 African American individuals 1,950 individuals Illumina [~ 2500000] 1 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST003882 Genome-wide genotyping array 2017-08-10 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Peak insulin response 2,337 Hispanic individuals, 2,159 European ancestry individuals, 332 Pima Indian ancestry individuals 739 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 9 peak insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008000 GCST004487 Genome-wide genotyping array 2017-08-21 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Acute insulin response 2,346 Hispanic individuals, 2,087 European ancestry individuals, 332 Pima Indian ancestry individuals 741 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 8 acute insulin response measurement http://www.ebi.ac.uk/efo/EFO_0006831 GCST004575 Genome-wide genotyping array 2017-08-10 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Insulin secretion rate 527 European ancestry individuals NA Affymetrix, Illumina [~ 39000000] (imputed) 2 insulin secretion measurement http://www.ebi.ac.uk/efo/EFO_0008001 GCST004488 Genome-wide genotyping array 2017-08-10 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Insulin disposition index 2,345 Hispanic individuals, 2,042 European ancestry individuals, 332 Pima Indian ancestry individuals 741 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 1 disposition index measurement http://www.ebi.ac.uk/efo/EFO_0006832 GCST004489 Genome-wide genotyping array 2018-12-06 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Insulin disposition index (BMI adjusted) 2,345 Hispanic individuals, 2,042 European ancestry individuals, 332 Pima Indian ancestry individuals 741 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 0 disposition index measurement http://www.ebi.ac.uk/efo/EFO_0006832 GCST006681 Genome-wide genotyping array 2018-12-06 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Peak insulin response (BMI and insulin secretion adjusted) 2,337 Hispanic individuals, 2,159 European ancestry individuals, 332 Pima Indian ancestry individuals 739 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 1 peak insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008000 GCST006675 Genome-wide genotyping array 2018-12-06 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Peak insulin response (insulin secretion adjusted) 2,337 Hispanic individuals, 2,159 European ancestry individuals, 332 Pima Indian ancestry individuals 739 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 1 peak insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008000 GCST006676 Genome-wide genotyping array 2018-12-06 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Acute insulin response (insulin secretion and BMI adjusted) 2,346 Hispanic individuals, 2,087 European ancestry individuals, 332 Pima Indian ancestry individuals 741 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 0 acute insulin response measurement http://www.ebi.ac.uk/efo/EFO_0006831 GCST006678 Genome-wide genotyping array 2018-12-06 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. Acute insulin response (insulin secretion adjusted) 2,346 Hispanic individuals, 2,087 European ancestry individuals, 332 Pima Indian ancestry individuals 741 European ancestry individuals Affymetrix, Illumina [~ 39000000] (imputed) 1 acute insulin response measurement http://www.ebi.ac.uk/efo/EFO_0006831 GCST006677 Genome-wide genotyping array 2018-12-06 28490609 Wood AR 2017-05-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/28490609 A Genome-Wide Association Study of IVGTT-Based Measures of First-Phase Insulin Secretion Refines the Underlying Physiology of Type 2 Diabetes Variants. insulin secretion rate (BMI adjusted) 527 European ancestry individuals NA Affymetrix, Illumina [~ 39000000] (imputed) 0 insulin secretion measurement http://www.ebi.ac.uk/efo/EFO_0008001 GCST006679 Genome-wide genotyping array 2017-08-18 28537267 Sapkota Y 2017-05-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28537267 Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism. Endometriosis 14,926 European ancestry cases, 189,715 European ancestry controls, 2,119 Japanese ancestry cases, 2,143 Japanese ancestry controls NA Affymetrix, Illumina [up to 6979035] (imputed) 35 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST004549 Genome-wide genotyping array 2017-07-18 28492228 Parks T 2017-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28492228 Association between a common immunoglobulin heavy chain allele and rheumatic heart disease risk in Oceania. Rheumatic heart disease 767 Oceanian ancestry cases, 1,462 Oceanian ancestry controls, 168 Fijian Indian cases, 151 Fijian Indian controls, 71 mixed and other ancestry cases, 236 mixed and other ancestry controls Illumina [5356509] (imputed) 2 rheumatic heart disease http://www.ebi.ac.uk/efo/EFO_1001161 GCST004366 Genome-wide genotyping array 2017-07-19 28494655 Duncan L 2017-05-12 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/28494655 Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa. Anorexia nervosa 3,495 European ancestry cases, 10,982 European ancestry controls NA Illumina [10641224] (imputed) 6 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST004367 Genome-wide genotyping array 2017-06-23 28424481 Sugiura-Ogasawara M 2017-04-20 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28424481 The first genome-wide association study identifying new susceptibility loci for obstetric antiphospholipid syndrome. Obstetric antiphospholipid syndrome 115 Japanese ancestry female cases, 419 Japanese ancestry male and female controls NA Affymetrix [426344] 15 antiphospholipid syndrome http://www.ebi.ac.uk/efo/EFO_0002689 GCST004227 Genome-wide genotyping array 2017-07-12 28453575 Hodonsky CJ 2017-04-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28453575 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Hematocrit 12,502 Hispanic/Latino individuals 7,106 Hispanic/Latino individuals Illumina [27801688] (imputed) 3 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST004330 Genome-wide genotyping array 2017-07-12 28453575 Hodonsky CJ 2017-04-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28453575 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Mean corpuscular hemoglobin concentration 12,502 Hispanic/Latino individuals 4,772 Hispanic/Latino individuals Illumina [27801688] (imputed) 9 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST004329 Genome-wide genotyping array 2017-07-12 28453575 Hodonsky CJ 2017-04-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28453575 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Red blood cell count 12,502 Hispanic/Latino individuals 4,772 Hispanic/Latino individuals Illumina [27801688] (imputed) 5 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST004332 Genome-wide genotyping array 2017-07-12 28453575 Hodonsky CJ 2017-04-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28453575 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Hemoglobin 12,502 Hispanic/Latino individuals 7,106 Hispanic/Latino individuals Illumina [27801688] (imputed) 3 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST004331 Genome-wide genotyping array 2017-07-12 28453575 Hodonsky CJ 2017-04-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28453575 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Red cell distribution width 12,502 Hispanic/Latino individuals 4,772 Hispanic/Latino individuals Illumina [27801688] (imputed) 1 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST004333 Genome-wide genotyping array 2017-07-12 28453575 Hodonsky CJ 2017-04-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28453575 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Mean corpuscular hemoglobin 12,502 Hispanic/Latino individuals 4,772 Hispanic/Latino individuals Illumina [27801688] (imputed) 14 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST004334 Genome-wide genotyping array 2017-07-12 28453575 Hodonsky CJ 2017-04-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28453575 Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos. Mean corpuscular volume 12,502 Hispanic/Latino individuals 4,772 Hispanic/Latino individuals Illumina [27801688] (imputed) 16 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST004335 Genome-wide genotyping array 2017-07-04 28441426 White CC 2017-04-25 PLoS Med www.ncbi.nlm.nih.gov/pubmed/28441426 Identification of genes associated with dissociation of cognitive performance and neuropathological burden: Multistep analysis of genetic, epigenetic, and transcriptional data. Residual cognition 979 European ancestry individuals NA Affymetrix, Illumina [~ 7000000] (imputed) 9 obsolete aging, cognition http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0003925 GCST004291 Genome-wide genotyping array 2018-01-15 27680694 Horikoshi M 2016-10-13 Nature www.ncbi.nlm.nih.gov/pubmed/27680694 Genome-wide associations for birth weight and correlations with adult disease. Birth weight 133,903 European ancestry individuals, 6,635 African American individuals, 420 Turkish ancestry individuals, 365 Moroccan ancestry individuals, 395 Surinamese ancestry individuals, 840 Chinese ancestry individuals. 9,799 European ancestry individuals, 1,449 Filipino ancestry individuals. Affymetrix, Illumina [at least 22434434] (imputed) 59 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST005146 Genome-wide genotyping array 2019-04-10 27680694 Horikoshi M 2016-10-13 Nature www.ncbi.nlm.nih.gov/pubmed/27680694 Genome-wide associations for birth weight and correlations with adult disease. Birth weight 133,903 European ancestry individuals 9,799 European ancestry individuals Affymetrix, Illumina [at least 22434434] (imputed) 2 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST007557 Genome-wide genotyping array 2017-09-19 28714907 Treutlein J 2017-07-17 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/28714907 Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. Alcohol dependence 1,331 German ancestry cases, 1,934 German ancestry controls NA Illumina [194024] 5 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST004756 Genome-wide genotyping array 2017-09-19 28714907 Treutlein J 2017-07-17 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/28714907 Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. Alcohol dependence or chronic alcoholic pancreatitis or alcohol-related liver cirrhosis 1,331 German ancestry alcohol dependence cases, 1,110 German ancestry cases with chronic alcoholic pancreatitis, 400 European ancestry cases with alcohol-related liver cirrhosis, 3,684 German ancestry controls NA Illumina [194024] 3 alcoholic liver cirrhosis, alcoholic pancreatitis, alcohol dependence http://www.ebi.ac.uk/efo/EFO_1000802, http://www.ebi.ac.uk/efo/EFO_1002013, http://purl.obolibrary.org/obo/MONDO_0007079 GCST004757 Genome-wide genotyping array 2017-09-19 28714907 Treutlein J 2017-07-17 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/28714907 Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis. Chronic alcoholic pancreatitis or alcohol-related cirrhosis 1,110 German ancestry cases with chronic alcoholic pancreatitis, 400 European ancestry cases with alcohol-related liver cirrhosis, 1,750 German ancestry controls NA Illumina [194024] 0 alcoholic liver cirrhosis, alcoholic pancreatitis http://www.ebi.ac.uk/efo/EFO_1000802, http://www.ebi.ac.uk/efo/EFO_1002013 GCST004755 Genome-wide genotyping array 2017-06-30 28437668 Jung J 2017-04-14 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/28437668 Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder. Venlafaxine response in generalised anxiety disorder (HAMA-A score reduction after 24 weeks) 98 European ancestry individuals NA Illumina [266820] (imputed) 2 response to venlafaxine http://www.ebi.ac.uk/efo/EFO_0006328 GCST004271 Genome-wide genotyping array 2017-06-30 28437668 Jung J 2017-04-14 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/28437668 Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder. Venlafaxine response in generalised anxiety disorder (HAMA-A score reduction after 12 weeks) 98 European ancestry individuals NA Illumina [266820] (imputed) 0 response to venlafaxine http://www.ebi.ac.uk/efo/EFO_0006328 GCST004272 Genome-wide genotyping array 2017-06-30 28437668 Jung J 2017-04-14 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/28437668 Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder. Venlafaxine response in generalised anxiety disorder (responders vs non-responders after 12 weeks) 98 European ancestry cases and controls NA Illumina [266820] (imputed) 3 response to venlafaxine http://www.ebi.ac.uk/efo/EFO_0006328 GCST004270 Genome-wide genotyping array 2017-06-30 28437668 Jung J 2017-04-14 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/28437668 Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder. Venlafaxine response in generalised anxiety disorder (remitters vs non-remitters after 24 weeks) 78 European ancestry cases, 20 European ancestry controls NA Illumina [266820] (imputed) 3 response to venlafaxine http://www.ebi.ac.uk/efo/EFO_0006328 GCST004273 Genome-wide genotyping array 2017-06-30 28437668 Jung J 2017-04-14 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/28437668 Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder. Venlafaxine response in generalised anxiety disorder (remitters vs non-remitters after 12 weeks) 98 European ancestry cases and controls NA Illumina [266820] (imputed) 4 response to venlafaxine http://www.ebi.ac.uk/efo/EFO_0006328 GCST004274 Genome-wide genotyping array 2017-06-30 28437668 Jung J 2017-04-14 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/28437668 Genome-wide association study of treatment response to venlafaxine XR in generalized anxiety disorder. Venlafaxine response in generalised anxiety disorder (responders vs non-responders after 24 weeks) 98 European ancestry cases and controls NA Illumina [266820] (imputed) 5 response to venlafaxine http://www.ebi.ac.uk/efo/EFO_0006328 GCST004275 Genome-wide genotyping array 2017-07-13 28471803 Choe EK 2017-05-03 Eur J Cancer Prev www.ncbi.nlm.nih.gov/pubmed/28471803 Search for genetic factor association with cancer-free prostate-specific antigen level elevation on the basis of a genome-wide association study in the Korean population. Elevated serum prostate-specific antigen levels in healthy men 2,841 Korean ancestry individuals 1,283 Korean ancestry individuals Affymetrix [584061] 2 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST004345 Genome-wide genotyping array 2018-01-15 29160300 Oetting WS 2017-11-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/29160300 Genome-wide association study identifies the common variants in CYP3A4 and CYP3A5 responsible for variation in tacrolimus trough concentration in Caucasian kidney transplant recipients. Tacrolimus trough concentration in kidney transplant patients 1,345 European ancestry individuals (homozygous for LoF CYPA3A5) NA Affymetrix [1221308] (imputed) 1 tacrolimus measurement http://www.ebi.ac.uk/efo/EFO_0008458 GCST005144 Genome-wide genotyping array 2018-01-29 29198719 Shaffer JR 2017-11-30 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29198719 Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment. Lobe attachment (rater-scored or self-reported) 66,741 European ancestry individuals, 5,062 Hispanic individuals, 2,857 Han Chinese ancestry individuals NA Illumina [at least 7383741] (imputed) 178 lobe attachment http://www.ebi.ac.uk/efo/EFO_0007667 GCST005192 Genome-wide genotyping array 2018-01-29 29198719 Shaffer JR 2017-11-30 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29198719 Multiethnic GWAS Reveals Polygenic Architecture of Earlobe Attachment. Lobe attachment (rater scored) 1791 European ancestry individuals, 5,062 Hispanic individuals, 2,857 Han Chinese ancestry individuals NA Illumina [at least 7383741] (imputed) 19 lobe attachment http://www.ebi.ac.uk/efo/EFO_0007667 GCST005193 Genome-wide genotyping array 2017-06-22 28386217 Ritter ML 2017-03-23 Front Mol Neurosci www.ncbi.nlm.nih.gov/pubmed/28386217 Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD). Attention deficit hyperactivity disorder and obsessive compulsive disorder 1406 European ancestry obsessive-compulsive disorder cases and 1,592 European ancestry controls from 1065 families, 2,960 European and unknown ancestry attention deficit hyperactivity disorder cases, 2,455 European and unknown ancestry parental and independent controls. NA Illumina [6598140] (imputed) 0 obsessive-compulsive disorder, attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0003888 GCST004223 Genome-wide genotyping array 2017-08-03 28485404 Jorgenson E 2017-05-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28485404 Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study. Alcohol consumption (drinks per week) 23,104 European ancestry non-drinker individuals, 47,967 European ancestry drinker individuals, 2,673 Hispanic/Latino non-drinker individuals, 4,374 Hispanic/Latino drinker individuals, 3,288 East Asian ancestry non-drinker individuals, 2,746 East Asian ancestry drinker individuals, 1,165 African American non-drinkers individuals, 1,310 African American drinker individuals.        NA Affymetrix [NR] (imputed) 8 alcohol consumption measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004329 GCST004405 Genome-wide genotyping array 2017-08-03 28485404 Jorgenson E 2017-05-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28485404 Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study. Alcohol consumption (drinkers vs non-drinkers) 23,104 European ancestry non-drinker individuals, 47,967 European ancestry drinker individuals, 2,673 Hispanic/Latino non-drinker individuals, 4,374 Hispanic/Latino drinker individuals, 3,288 East Asian ancestry non-drinker individuals, 2,746 East Asian ancestry drinker individuals, 1,165 African American non-drinkers individuals, 1,310 African American drinker individuals.        NA Affymetrix [NR] (imputed) 7 alcohol consumption measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004329 GCST004404 Genome-wide genotyping array 2018-12-17 29188820 Kotnik P 2017-11-30 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/29188820 Identification of novel alleles associated with insulin resistance in childhood obesity using pooled-DNA genome-wide association study approach. Childhood insulin resistance 98 cases, 100 controls 79 cases, 78 controls Illumina [NR] 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST006800 Genome-wide genotyping array 2017-07-14 28472463 Mullin BH 2017-05-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28472463 Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation. Bone ultrasound measurement (velocity of sound) 1,268 whole genome sequenced European ancestry women, 8,880 European ancestry women, 6,479 European ancestry men NA Illumina [11973598] (imputed) 21 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST004350 Genome-wide genotyping array 2017-07-14 28472463 Mullin BH 2017-05-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28472463 Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation. Bone ultrasound measurement (broadband ultrasound attenuation) 1,268 whole genome sequenced European ancestry women, 8,880 European ancestry women, 6,479 European ancestry men NA Illumina [11973598] (imputed) 28 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST004351 Genome-wide genotyping array 2017-08-07 27082954 Ward-Caviness CK 2016-04-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/27082954 Genetic Variants in the Bone Morphogenic Protein Gene Family Modify the Association between Residential Exposure to Traffic and Peripheral Arterial Disease. Peripheral arterial disease (traffic-related air pollution interaction) 104 European ancestry cases, 1,519 European ancestry controls, 34 African American cases, 520 African American controls NA Illumina [905956] 159 peripheral arterial disease, traffic air pollution measurement http://www.ebi.ac.uk/efo/EFO_0004265, http://www.ebi.ac.uk/efo/EFO_0007908 GCST004482 Genome-wide genotyping array 2017-07-24 28498854 Liang J 2017-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28498854 Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Systolic blood pressure Up to 31,155 African individuals Up to 4,187 African individuals, up to 14,016 Korean ancestry individuals, up to 23,914 European ancestry individuals, up to 12,278 Hispanic individuals Affymetrix, Illumina [at least 30072738] (imputed) 9 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST004385 Genome-wide genotyping array 2017-07-24 28498854 Liang J 2017-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28498854 Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Diastolic blood pressure Up to 31,155 African individuals Up to 4,187 African individuals, up to 14,016 Korean ancestry individuals, up to 23,914 European ancestry individuals, up to 12,278 Hispanic individuals Affymetrix, Illumina [at least 30072738] (imputed) 15 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST004386 Genome-wide genotyping array 2017-07-24 28498854 Liang J 2017-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28498854 Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Pulse pressure Up to 31,155 African individuals Up to 4,187 African individuals, up to 14,016 Korean ancestry individuals, up to 23,914 European ancestry individuals, up to 12,278 Hispanic individuals Affymetrix, Illumina [at least 30072738] (imputed) 9 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST004387 Genome-wide genotyping array 2017-07-24 28498854 Liang J 2017-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28498854 Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Hypertension 18,440 African individuals 2,375 African individuals, 3,718 Korean ancestry individuals, 9,348 European ancestry individuals, 3,445 Hispanic individuals Affymetrix, Illumina [at least 30072738] (imputed) 7 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST004384 Genome-wide genotyping array 2017-07-24 28498854 Liang J 2017-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28498854 Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations. Blood pressure traits (multi-trait analysis) Up to 31,155 African individuals Up to 4,187 African individuals, up to 14,016 Korean ancestry individuals, up to 23,914 European ancestry individuals, up to 12,278 Hispanic individuals Affymetrix, Illumina [at least 30072738] (imputed) 32 pulse pressure measurement, diastolic blood pressure, systolic blood pressure, hypertension http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0000537 GCST004388 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. Interleukin-6 (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 2 fatty acid measurement, interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004810 GCST004814 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. Lipoprotein-associated phospholipase A2 (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 0 fatty acid measurement, lipoprotein-associated phospholipase A(2) measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004746 GCST004816 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. Intercellular adhesion molecule 1 (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 1 fatty acid measurement, ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004520 GCST004818 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. Cellular adhesion molecule (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 1 fatty acid measurement, cellular adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0008353 GCST004820 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. Monocyte chemoattractant protein-1 (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 1 fatty acid measurement, CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004749 GCST004821 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. Tumor necrosis factor receptor II (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 1 fatty acid measurement, tumor necrosis factor receptor II measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0008384 GCST004817 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. C-reactive protein (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 2 fatty acid measurement, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004458 GCST004815 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. Osteoprotegerin (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 0 fatty acid measurement, osteoprotegerin measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0005918 GCST004819 Genome-wide genotyping array 2017-09-29 28820441 Veenstra J 2017-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/28820441 Genome-Wide Interaction Study of Omega-3 PUFAs and Other Fatty Acids on Inflammatory Biomarkers of Cardiovascular Health in the Framingham Heart Study. P-Selectin (red blood cell fatty acid level interaction) 2,703 individuals NA Affymetrix [2500000] (imputed) 0 fatty acid measurement, P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0008254 GCST004822 Genome-wide genotyping array 2017-09-23 28828242 Dajani R 2017-08-17 PeerJ www.ncbi.nlm.nih.gov/pubmed/28828242 Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations. Type 2 diabetes 67 Greater Middle Eastern ancestry cases, 214 Greater Middle Eastern ancestry controls 1,952 European ancestry cases, 2,960 European ancestry controls Illumina [645000] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004782 Genome-wide genotyping array 2017-07-13 28421636 Dennis J 2017-04-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/28421636 Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels. Tissue factor pathway inhibitor levels 251 French Canadian individuals from 5 families 1,033 European ancestry individuals Illumina [6159088] (imputed) 0 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST004344 Genome-wide genotyping array 2017-07-12 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 1, breadth of lateral portion of upper face) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 22 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST004328 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 10, width of nasal floor) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 14 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST004314 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 3, length of philtrum) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 16 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST004307 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 15, philtrum width) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 26 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST004319 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 16) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 15 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST004320 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 17, height of vermillion upper lip) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 26 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST004321 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 18) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 21 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST004322 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 19) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 32 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST004323 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 20) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 22 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST004324 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 2, vertical position of orbits relative to midface) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 16 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST004306 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 4, facial height related to vertical position of gnathion) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 20 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST004308 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 5, width of mouth relative to central midface) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 17 mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007955 GCST004309 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 6, height of vermillion lower lip) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 22 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST004310 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 7, width of cartilaginous portion of nose) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 17 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST004311 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 8, orbital inclination due to vertical and horizontal position of exocanthion) 2,187 European ancestry individuals NA Illumina [34985077] (imputed) 19 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST004312 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 9, facial height related to vertical position of nasion) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 19 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST004313 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 11, projection of the nose) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 19 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST004315 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 12, vertical position of sublabial sulcus relative to central midface) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 18 mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007955 GCST004316 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 13, vertical position of alar curvature relative to upper lip) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 16 nose morphology measurement, mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843, http://www.ebi.ac.uk/efo/EFO_0007955 GCST004317 Genome-wide genotyping array 2017-07-11 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 14, intercanthal width) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 21 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST004318 Genome-wide genotyping array 2017-07-12 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 21, depth of nasal alae) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 25 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST004325 Genome-wide genotyping array 2017-07-12 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 22) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 20 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST004326 Genome-wide genotyping array 2017-07-12 28441456 Lee MK 2017-04-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/28441456 Genome-wide association study of facial morphology reveals novel associations with FREM1 and PARK2. Facial morphology (factor 23) 2,187 European ancestry individuals NA Illumina [10677593] (imputed) 16 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST004327 Genome-wide genotyping array 2017-04-21 27839851 Lind L 2016-11-11 Environ Int www.ncbi.nlm.nih.gov/pubmed/27839851 Genetic and methylation variation in the CYP2B6 gene is related to circulating p,p'-dde levels in a population-based sample. DDT metabolite (p,p'-DDE levels) up to 1,016 European ancestry individuals NA Illumina [NR] (imputed) 2 DDT metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007886 GCST003923 Genome-wide genotyping array 2017-08-02 28512992 Joo YB 2017-05-16 Int J Rheum Dis www.ncbi.nlm.nih.gov/pubmed/28512992 Association of CD8+ T-cells with bone erosion in patients with rheumatoid arthritis. Bone erosion in rheumatoid arthritis 385 Korean ancestry cases, 326 Korean ancestry controls NA Illumina [439289] 2 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST004400 Genome-wide genotyping array 2017-11-06 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Dehydroepiandrosterone sulphate levels 5,414 European ancestry women, 4,308 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 2 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST004941 Genome-wide genotyping array 2017-11-06 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Glycated hemoglobin levels 5,288 European ancestry women, 4,148 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 2 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST004939 Genome-wide genotyping array 2017-11-06 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Alanine transaminase levels 5,458 European ancestry women, 4,273 European ancestry men up to 9,888 European ancestry individuals, up to 16,013 individuals Illumina [at least 23756480] (imputed) 1 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST004940 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Serum albumin levels 5,501 European ancestry women, 4,323 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST005059 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Serum alkaline phosphatase levels 5,451 European ancestry women, 4,282 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST005061 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Fibrinogen levels 5,468 European ancestry women, 4,294 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST005062 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Aspartate aminotransferase levels 5,321 European ancestry women, 4,142 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST005064 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Cholesterol, total 5,495 European ancestry women, 4,322 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST005065 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Creatinine levels 5,497 European ancestry women, 4,306 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST005066 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Gamma glutamyl transferase levels 5,467 European ancestry women, 4,280 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST005069 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. HDL cholesterol 5,482 European ancestry women, 4,314 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005058 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Hemoglobin levels 5,392 European ancestry women, 4,275 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST005060 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. C-reactive protein levels 5,350 European ancestry women, 4,191 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST005067 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Insulin-like growth factor 1 levels 5,455 European ancestry women, 4,277 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST005071 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Ferritin levels 5,499 European ancestry women, 4,319 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST005072 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Testosterone levels 4,259 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST005074 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Triglyceride levels 5,482 European ancestry women, 4,263 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005073 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Urea levels 5,498 European ancestry women, 4,320 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST005070 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. LDL cholesterol up to 5,574 European ancestry women, up to 4,387 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005068 Genome-wide genotyping array 2017-12-19 28887542 Prins BP 2017-09-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28887542 Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations. Glomerular filtration rate up to 5,574 European ancestry women, up to 4,387 European ancestry men 9,888 European ancestry individuals, 16,013 individuals Illumina [at least 23756480] (imputed) 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST005063 Genome-wide genotyping array 2018-04-25 23749187 Cortes A 2013-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23749187 Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Ankylosing spondylitis 9,069 European ancestry cases, 1,550 East Asian ancestry cases, 13,578 European ancestry controls, 1,567 East Asian ancestry controls NA Illumina [128935] 70 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST005529 Targeted genotyping array [ImmunoChip] 2018-04-25 23749187 Cortes A 2013-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23749187 Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Ankylosing spondylitis (SNP x SNP interaction) 9,069 European ancestry cases, 13,578 European ancestry controls NA Illumina [128935] 2 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST005530 Targeted genotyping array [ImmunoChip] 2017-02-15 27587472 Postmus I 2016-09-01 J Med Genet www.ncbi.nlm.nih.gov/pubmed/27587472 Meta-analysis of genome-wide association studies of HDL cholesterol response to statins. Response to statins (HDL cholesterol change) 16,769 European ancestry individuals 10,951 European ancestry individuals Affymetrix, Illumina, Perlegen [up to 2500000] (imputed) 2 HDL cholesterol change measurement, response to statin http://www.ebi.ac.uk/efo/EFO_0007805, http://purl.obolibrary.org/obo/GO_0036273 GCST003617 Genome-wide genotyping array 2017-03-20 28171663 Huo D 2016-09-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28171663 Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. Breast cancer 3962 African American cases, 711 African ancestry cases, 4,150 African ancestry controls, 624 African ancestry controls 1,984 African American cases, 2,939 African American controls Illumina [16147413] (imputed) 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST003782 Genome-wide genotyping array 2017-03-20 28171663 Huo D 2016-09-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28171663 Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. Breast cancer (estrogen-receptor positive) 1795 African American cases, 99 African ancestry cases, 4,150 African American controls, 624 African ancestry controls 1093 African American cases, 2939 African American controls Illumina [16147413] (imputed) 1 estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_1000649 GCST003781 Genome-wide genotyping array 2017-03-20 28171663 Huo D 2016-09-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28171663 Genome-wide association studies in women of African ancestry identified 3q26.21 as a novel susceptibility locus for oestrogen receptor negative breast cancer. Breast cancer (estrogen-receptor negative) 1349 African American cases, 42 African ancestry cases, 4,150 African American controls, 624 African ancestry controls 573 African American cases, 2,939 African American controls Illumina [16147413] (imputed) 2 estrogen-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_1000650 GCST003780 Genome-wide genotyping array 2017-05-12 27824142 Lin H 2016-11-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27824142 Gene-gene Interaction Analyses for Atrial Fibrillation. Atrial fibrillation (SNPxSNP interaction) 8,173 European ancestry cases, 65,237 European ancestry controls 2,363 European ancestry cases, 114,746 European ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004018 Genome-wide genotyping array 2017-03-14 27599772 Ram R 2016-09-07 Clin Genet www.ncbi.nlm.nih.gov/pubmed/27599772 A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia. Hypertriglyceridemia 927 Saudi Arabian ancestry cases, 3,159 Saudi Arabian ancestry controls 317 Saudi Arabian ancestry cases, 1,098 Saudi Arabian ancestry controls Affymetrix [~ 8000000] (imputed) 10 Hypertriglyceridemia http://www.ebi.ac.uk/efo/EFO_0004211 GCST003743 Genome-wide genotyping array 2017-08-30 28495826 Williams SR 2017-06-01 Stroke www.ncbi.nlm.nih.gov/pubmed/28495826 Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke. vWF levels in ischaemic stroke and hyperhomocysteinaemia 1,931 European and unknown ancestry individuals NA NR [NR] (imputed) 3 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST004598 Genome-wide genotyping array 2017-03-14 27601451 Sanders AE 2016-09-06 J Dent Res www.ncbi.nlm.nih.gov/pubmed/27601451 Chronic Periodontitis Genome-wide Association Study in the Hispanic Community Health Study / Study of Latinos. Chronic periodontitis (mean interproximal clinical attachment level) 10,935 Hispanic individuals 4,402 European ancestry individuals, 908 African American individuals Illumina [~ 20000000] (imputed) 5 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST003744 Genome-wide genotyping array 2017-07-21 28533516 Cantor RM 2017-05-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28533516 ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains. Restricted and repetitive behaviours in autism spectrum disorder 4,664 European ancestry children from 2,145 families NA Illumina [at least 3972813] (imputed) 1 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST004377 Genome-wide genotyping array 2018-12-06 23603763 Liu JZ 2013-06-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23603763 Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Primary sclerosing cholangitis 3,789 European ancestry cases, 25,079 European ancestry controls NA Illumina [140322] (imputed) 19 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST006670 Targeted genotyping array [ImmunoChip] 2018-05-04 23603763 Liu JZ 2013-06-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23603763 Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis. Primary sclerosing cholangitis associated immune-mediated diseases (Crohn's disease, celiac disease, psoriasis, rheumatoid arthritis, sarcoidosis, type 1 diabetes or ulcerative colitis) (pleiotropy) 6,333 European ancestry Crohn's disease cases, 4,533 European ancestry celiac disease cases, 2,529 European ancestry psoriasis cases, 5,539 European ancestry rheumatoid arthritis cases, 568 European ancestry sarcoidosis cases, 7,514 European ancestry type I diabetes cases, 6,687 European ancestry ulcerative colitis cases, 3,789 European ancestry sclerosing cholangitis cases, 106,357 European ancestry controls NA Illumina [at least 130422] 0 rheumatoid arthritis, sarcoidosis, type 1 diabetes mellitus, psoriasis, celiac disease, ulcerative colitis, Crohn's disease, sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0000685, http://purl.obolibrary.org/obo/MONDO_0019338, http://purl.obolibrary.org/obo/MONDO_0005147, http://www.ebi.ac.uk/efo/EFO_0000676, http://www.ebi.ac.uk/efo/EFO_0001060, http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0000384, http://www.ebi.ac.uk/efo/EFO_0004268 GCST005563 Genome-wide genotyping array, Targeted genotyping array 2017-09-14 28468790 Agopian AJ 2017-06-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28468790 Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. Conotruncal heart defects (inherited effects) 483 European ancestry trios, 406 European ancestry cases, 2,976 European ancestry controls, 355 European and other ancestry trios, 187 non-European ancestry trios. NA Illumina [at least 4756722] (imputed) 10 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST004720 Genome-wide genotyping array 2017-09-14 28468790 Agopian AJ 2017-06-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28468790 Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. Left ventricular obstructive tract defect (inherited effect) 247 European ancestry trios, 70 non-European ancestry trios, 192 European and other ancestry trios NA Illumina [at least 4483243] (imputed) 15 congenital left-sided heart lesions http://www.ebi.ac.uk/efo/EFO_0005938 GCST004719 Genome-wide genotyping array 2017-09-14 28468790 Agopian AJ 2017-06-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28468790 Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. Conotruncal heart defects (maternal effects) up to 838 European ancestry trios NA Illumina [at least 4756722] (imputed) 22 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST004723 Genome-wide genotyping array 2017-09-14 28468790 Agopian AJ 2017-06-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28468790 Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. Left ventricular obstructive tract defect (maternal effect) up to 439 European ancestry trios NA Illumina [at least 4756722] (imputed) 9 congenital left-sided heart lesions http://www.ebi.ac.uk/efo/EFO_0005938 GCST004722 Genome-wide genotyping array 2017-09-14 28468790 Agopian AJ 2017-06-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28468790 Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. Congenital heart disease (inherited effect) 1,119 European ancestry trios, 406 European ancestry cases, 2,976 European ancestry controls, 415 non-European ancestry trios NA Illumina [at least 4756772] (imputed) 10 congenital heart disease http://www.ebi.ac.uk/efo/EFO_0005207 GCST004718 Genome-wide genotyping array 2017-09-14 28468790 Agopian AJ 2017-06-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28468790 Genome-Wide Association Studies and Meta-Analyses for Congenital Heart Defects. Congenital heart disease (maternal effect) 1,119 European ancestry trios NA Illumina [at least 4756722] (imputed) 20 congenital heart disease http://www.ebi.ac.uk/efo/EFO_0005207 GCST004721 Genome-wide genotyping array 2017-08-09 28470677 Tang H 2017-05-03 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/28470677 Genetic polymorphisms associated with pancreatic cancer survival: a genome-wide association study. Survival in pancreatic cancer 868 European ancestry cases 820 European ancestry cases NR [7738399] (imputed) 61 overall survival, pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0002618 GCST004485 Genome-wide genotyping array 2017-06-19 28459102 Zhang S 2016-04-20 JDR Clin Trans Res www.ncbi.nlm.nih.gov/pubmed/28459102 The Novel ASIC2 Locus is Associated with Severe Gingival Inflammation. Severe gingival inflammation 4,077 European American individuals NA Affymetrix [2500000] (imputed) 5 Gingival bleeding http://purl.obolibrary.org/obo/HP_0000225 GCST004198 Genome-wide genotyping array 2018-04-26 25751624 Onengut-Gumuscu S 2015-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25751624 Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers. Type 1 diabetes 6,683 European ancestry cases, 12,173 European ancestry controls, 2,601 European ancestry affected sibling pair families, 69 European ancestry trios NA Illumina [135870] 51 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST005536 Targeted genotyping array [ImmunoChip] 2018-08-16 22205395 Tekola Ayele F 2011-12-29 Immunogenetics www.ncbi.nlm.nih.gov/pubmed/22205395 Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans. Interleukin-10 levels 704 African American individuals 425 West African individuals Affymetrix [5396780] (imputed) 15 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST006102 Genome-wide genotyping array 2018-08-16 22205395 Tekola Ayele F 2011-12-29 Immunogenetics www.ncbi.nlm.nih.gov/pubmed/22205395 Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans. Interleukin-6 levels 697 African American individuals NA Affymetrix [5396780] (imputed) 20 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST006103 Genome-wide genotyping array 2018-08-16 22205395 Tekola Ayele F 2011-12-29 Immunogenetics www.ncbi.nlm.nih.gov/pubmed/22205395 Genome-wide associated loci influencing interleukin (IL)-10, IL-1Ra, and IL-6 levels in African Americans. Interleukin-1-receptor antagonist levels 706 African American individuals NA Affymetrix [5396780] (imputed) 7 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST006104 Genome-wide genotyping array 2019-04-15 29045471 Robiou-du-Pont S 2017-10-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29045471 Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study. Blood pressure (parental or offspring effect) 515 children, 406 mothers and 237 fathers NA Illumina [up to 196725] 0 blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006943 GCST007577 Targeted genotyping array [Cardio-MetaboChip] 2017-08-02 28580392 Taylor KC 2016-08-27 Bone Rep www.ncbi.nlm.nih.gov/pubmed/28580392 A genome-wide association study meta-analysis of clinical fracture in 10,012 African American women. Bone fracture in osteoporosis up to 10,305 African American women NA Affymetrix, Illumina [~ 2500000] (imputed) 9 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST004403 Genome-wide genotyping array 2017-03-20 27588450 Mahajan A 2016-09-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27588450 Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity. Glomerular filtration rate 23,553 European ancestry individuals, 23,536 Japanese individuals, 16,325 Hispanic individuals, 8,224 African American individuals NA Affymetrix, Illumina [at least 6581000] (imputed) 42 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST003790 Genome-wide genotyping array 2017-04-23 27595289 Goyal RK 2016-09-05 Bone Marrow Transplant www.ncbi.nlm.nih.gov/pubmed/27595289 Novel HLA-DP region susceptibility loci associated with severe acute GvHD. Acute graft versus host disease in bone marrow transplantation (recipient effect) 291 European ancestry recipients with acute graft versus host disease, 288 European ancestry recipients without acute graft versus host disease NA Affymetrix [905761] 19 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST003941 Genome-wide genotyping array 2017-04-23 27595289 Goyal RK 2016-09-05 Bone Marrow Transplant www.ncbi.nlm.nih.gov/pubmed/27595289 Novel HLA-DP region susceptibility loci associated with severe acute GvHD. Acute graft versus host disease in bone marrow transplantation (donor effect) 315 European ancestry donors (recipients with acute graft versus host disease), 341 European ancestry donors (recipients without graft versus host disease) NA Affymetrix [905761] 3 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST003942 Genome-wide genotyping array 2017-12-05 28724990 Zillikens MC 2017-07-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28724990 Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Appendicular lean mass 27,488 European ancestry individuals, 842 Old Order Amish individuals 42,360 European ancestry individuals, 380 African American individuals, 2,350 Korean ancestry individuals Affymetrix, Illumina [at least 1912063] (imputed) 5 appendicular lean mass http://www.ebi.ac.uk/efo/EFO_0004980 GCST005037 Genome-wide genotyping array 2017-12-05 28724990 Zillikens MC 2017-07-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28724990 Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Lean body mass 37,450 European ancestry individuals, 842 Old Order Amish individuals 47,227 European ancestry individuals, 380 African American individuals, 8,034 Korean ancestry individuals, 7,834 Indian ancestry individuals Affymetrix, Illumina [at least 1912063] (imputed) 7 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST005036 Genome-wide genotyping array 2017-11-02 29036319 Qi H 2017-09-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29036319 Discovery of susceptibility loci associated with tuberculosis in Han Chinese. Tuberculosis 972 Chinese ancestry cases, 1,316 Gambian ancestry cases, 1,537 Chinese ancestry controls, 1,382 Gambian ancestry controls NA Illumina [7333833] (imputed) 12 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST004922 Genome-wide genotyping array 2017-11-02 29036319 Qi H 2017-09-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29036319 Discovery of susceptibility loci associated with tuberculosis in Han Chinese. Tuberculosis 972 Chinese ancestry cases, 1,537 Chinese ancestry controls 3,338 Chinese ancestry cases, 4,849 Chinese ancestry controls Illumina [691388] 3 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST004923 Genome-wide genotyping array 2017-02-24 27416945 Walford GA 2016-07-14 Diabetes www.ncbi.nlm.nih.gov/pubmed/27416945 Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci. Modified Stumvoll Insulin Sensitivity Index (BMI interaction) 16,753 European ancestry individuals 13,354 European ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 12 insulin sensitivity measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0004340 GCST003659 Genome-wide genotyping array 2018-01-22 27416945 Walford GA 2016-07-14 Diabetes www.ncbi.nlm.nih.gov/pubmed/27416945 Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci. Modified Stumvoll Insulin Sensitivity Index 16,753 European ancestry individuals 13,354 European ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 1 insulin sensitivity measurement http://www.ebi.ac.uk/efo/EFO_0004471 GCST005178 Genome-wide genotyping array 2017-02-24 27416945 Walford GA 2016-07-14 Diabetes www.ncbi.nlm.nih.gov/pubmed/27416945 Genome-Wide Association Study of the Modified Stumvoll Insulin Sensitivity Index Identifies BCL2 and FAM19A2 as Novel Insulin Sensitivity Loci. Modified Stumvoll Insulin Sensitivity Index (model adjusted for BMI) 16,753 European ancestry individuals 13,354 European ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 4 insulin sensitivity measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0004340 GCST003658 Genome-wide genotyping array 2017-03-13 27527254 Gharahkhani P 2016-08-12 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/27527254 Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis. Barrett's esophagus 6,167 European ancestry cases, 17,159 European ancestry controls NA Illumina [11942825] (imputed) 5 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST003738 Genome-wide genotyping array 2017-03-13 27527254 Gharahkhani P 2016-08-12 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/27527254 Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis. Esophageal adenocarcinoma 4,112 European ancestry cases, 17,159 European ancestry controls NA Illumina [13074274] (imputed) 5 esophageal adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000478 GCST003739 Genome-wide genotyping array 2017-03-13 27527254 Gharahkhani P 2016-08-12 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/27527254 Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis. Barrett's esophagus or Esophageal adenocarcinoma 6,167 European ancestry Barrett's oesophagus cases, 4,112 European ancestry esophageal adenocarcinoma cases, 17,159 European ancestry controls NA Illumina [11951684] (imputed) 14 esophageal adenocarcinoma, Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000478, http://www.ebi.ac.uk/efo/EFO_0000280 GCST003740 Genome-wide genotyping array 2017-10-19 28871152 Sofer T 2017-09-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28871152 Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos. Diastolic blood pressure 12,278 Hispanic individuals 2,764 Brazilian individuals, at least 22,000 African American individuals, at least 155,786 European ancestry individuals Illumina [27887661] (imputed) 1 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST004890 Genome-wide genotyping array 2017-10-19 28871152 Sofer T 2017-09-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28871152 Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos. Mean arterial pressure 12,278 Hispanic individuals 2,764 Brazilian individuals, at least 22,000 African American individuals, at least 155,786 European ancestry individuals Illumina [27887661] (imputed) 1 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST004891 Genome-wide genotyping array 2017-10-19 28871152 Sofer T 2017-09-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28871152 Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos. Systolic blood pressure 12,278 Hispanic individuals 2,764 Brazilian individuals, at least 22,000 African American individuals, at least 155,786 European ancestry individuals Illumina [27887661] (imputed) 1 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST004888 Genome-wide genotyping array 2017-10-19 28871152 Sofer T 2017-09-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28871152 Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos. Pulse pressure 12,278 Hispanic individuals 2,764 Brazilian individuals, at least 22,000 African American individuals, at least 155,786 European ancestry individuals Illumina [27887661] (imputed) 0 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST004892 Genome-wide genotyping array 2017-10-19 28871152 Sofer T 2017-09-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28871152 Genome-Wide Association Study of Blood Pressure Traits by Hispanic/Latino Background: the Hispanic Community Health Study/Study of Latinos. Hypertension 12,278 Hispanic individuals 2,764 Brazilian individuals, at least 22,000 African American individuals, at least 155,786 European ancestry individuals Illumina [27887661] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST004889 Genome-wide genotyping array 2017-02-08 27577874 Evans DS 2016-08-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27577874 Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans. QRS duration up to 13,031 African American individuals, 40,407 European ancestry individuals NA Affymetrix, Illumina [2955816] (imputed) 54 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST003598 Genome-wide genotyping array 2017-09-21 28736931 Rotroff DM 2017-07-24 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/28736931 Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. HDL cholesterol change in response to fenofibrate in statin-treated type 2 diabetes 781 European ancestry individuals, 138 African American ancestry individuals, 345 unknown ancestry individuals Affymetrix, Illumina [8129838] (imputed) 6 HDL cholesterol change measurement, response to simvastatin, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007805, http://purl.obolibrary.org/obo/GO_1903491, http://purl.obolibrary.org/obo/GO_1901557 GCST004763 Genome-wide genotyping array 2017-09-21 28736931 Rotroff DM 2017-07-24 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/28736931 Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. LDL cholesterol change in response to fenofibrate in statin-treated type 2 diabetes 781 European ancestry individuals, 138 African American ancestry individuals, 345 unknown ancestry individuals Affymetrix, Illumina [8129838] (imputed) 7 LDL cholesterol change measurement, response to simvastatin, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007804, http://purl.obolibrary.org/obo/GO_1903491, http://purl.obolibrary.org/obo/GO_1901557 GCST004764 Genome-wide genotyping array 2017-09-21 28736931 Rotroff DM 2017-07-24 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/28736931 Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. Total cholesterol change in response to fenofibrate in statin-treated type 2 diabetes 781 European ancestry individuals, 138 African American ancestry individuals, 345 unknown ancestry individuals Affymetrix, Illumina [8129838] (imputed) 35 response to simvastatin, total cholesterol change measurement, response to fenofibrate http://purl.obolibrary.org/obo/GO_1903491, http://www.ebi.ac.uk/efo/EFO_0007806, http://purl.obolibrary.org/obo/GO_1901557 GCST004765 Genome-wide genotyping array 2017-09-21 28736931 Rotroff DM 2017-07-24 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/28736931 Genetic Variants in HSD17B3, SMAD3, and IPO11 Impact Circulating Lipids in Response to Fenofibrate in Individuals With Type 2 Diabetes. Triglyceride change in response to fenofibrate in statin-treated type 2 diabetes 781 European ancestry individuals, 138 African American ancestry individuals, 345 unknown ancestry individuals Affymetrix, Illumina [8129838] (imputed) 26 triglyceride change measurement, response to simvastatin, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007681, http://purl.obolibrary.org/obo/GO_1903491, http://purl.obolibrary.org/obo/GO_1901557 GCST004766 Genome-wide genotyping array 2017-09-21 28743860 Medina-Gomez C 2017-07-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28743860 Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus. TB-LM or TBLH-BMD (pleiotropy) 8,327 European ancestry individuals, 2,087 individuals NA Illumina [2276811] (imputed) 12 bone density, lean body mass http://www.ebi.ac.uk/efo/EFO_0003923, http://www.ebi.ac.uk/efo/EFO_0004995 GCST004771 Genome-wide genotyping array 2017-09-21 28743860 Medina-Gomez C 2017-07-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28743860 Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus. Lean body mass 8,327 European ancestry individuals, 2,087 individuals NA Illumina [2276811] (imputed) 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST004770 Genome-wide genotyping array 2017-09-21 28743860 Medina-Gomez C 2017-07-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28743860 Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus. Bone mineral density (paediatric, total body less head) 8,327 European ancestry individuals, 2,087 individuals NA Illumina [2276811] (imputed) 10 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST004772 Genome-wide genotyping array 2020-12-01 27432226 Kar SP 2016-07-17 Cancer Discov www.ncbi.nlm.nih.gov/pubmed/27432226 Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types. Breast cancer, ovarian cancer or prostate cancer (pleiotropy) 62,533 European ancestry breast cancer female cases, 60,976 European ancestry controls, 15,437 European ancestry invasive epithelial ovarian cancer female cases, 30,845 European ancestry controls, 34,379 European ancestry prostate cancer male cases, 33,164 European ancestry controls NA Illumina [NR] 18 prostate carcinoma, breast carcinoma, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001663, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0001075 GCST010797 Targeted genotyping array 2017-06-27 28560309 Lee E 2017-04-23 Alzheimers Dement (Amst) www.ncbi.nlm.nih.gov/pubmed/28560309 Single-nucleotide polymorphisms are associated with cognitive decline at Alzheimer's disease conversion within mild cognitive impairment patients. Accelerated cognitive decline after conversion of mild cognitive impairment to Alzheimer's disease (Alzhiemer's diagnosis trajectory interaction) 242 European ancestry individuals NA Illumina [5908215] (imputed) 11 Alzheimer disease, cognitive decline measurement, Cognitive impairment http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0007710, http://purl.obolibrary.org/obo/HP_0100543 GCST004253 Genome-wide genotyping array 2017-07-04 28445677 Steri M 2017-04-27 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/28445677 Overexpression of the Cytokine BAFF and Autoimmunity Risk. Multiple sclerosis 2,273 Sardinian cases, 2,148 Sardinian controls 6,840 European ancestry cases, 661 Sardinian cases, 3,176 cases, 6,044 European ancestry controls, 1,244 Sardinian controls, 2,958 controls Affymetrix [~ 12200000] (imputed) 5 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST004290 Genome-wide genotyping array 2017-09-05 28749367 Gondalia R 2017-06-08 Environ Health Perspect www.ncbi.nlm.nih.gov/pubmed/28749367 Genome-wide Association Study of Susceptibility to Particulate Matter-Associated QT Prolongation. QT interval (ambient particulate matter interaction) 14,889 European ancestry individuals, 5,707 African American individuals, 1,562 Hispanic individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 6 QT interval, particulate matter air pollution measurement http://www.ebi.ac.uk/efo/EFO_0004682, http://www.ebi.ac.uk/efo/EFO_0008255 GCST004642 Genome-wide genotyping array 2017-08-08 28439531 Aslibekyan S 2017-03-08 J Nutr Intermed Metab www.ncbi.nlm.nih.gov/pubmed/28439531 Genome- and CD4+ T-cell methylome-wide association study of circulating trimethylamine-N-oxide in the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN). Plasma trimethylamine N-oxide levels 626 European ancestry individuals NA Affymetrix [9432837] (imputed) 12 plasma trimethylamine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0005691 GCST004484 Genome-wide genotyping array 2017-02-25 27418160 van 't Hof FN 2016-07-14 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/27418160 Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms. Intracranial, abdominal aortic or thoracic aortic aneurysm (pleiotropy) 1,516 European ancestry intracranial aneurysm cases, 818 European ancestry abdominal aortic aneurysm cases, 760 European ancestry thoracic aortic aneurysm cases, 9,507 European ancestry controls NA Illumina [9245988] (imputed) 4 thoracic aortic aneurysm, Abdominal Aortic Aneurysm, brain aneurysm http://www.ebi.ac.uk/efo/EFO_0004282, http://www.ebi.ac.uk/efo/EFO_0004214, http://www.ebi.ac.uk/efo/EFO_0003870 GCST003683 Genome-wide genotyping array 2018-04-26 25337690 Redler S 2015-03-01 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/25337690 Immunochip-based analysis: high-density genotyping of immune-related loci sheds further light on the autoimmune genetic architecture of alopecia areata. Alopecia areata 767 European ancestry cases, 1,475 European ancestry controls 1,016 European ancestry cases, 1,060 European ancestry controls Illumina [146703] 2 alopecia areata http://www.ebi.ac.uk/efo/EFO_0004192 GCST005539 Targeted genotyping array [ImmunoChip] 2017-02-03 27439200 Nieuwenhuis MA 2016-07-20 Allergy www.ncbi.nlm.nih.gov/pubmed/27439200 Combining genomewide association study and lung eQTL analysis provides evidence for novel genes associated with asthma. Bronchial hyperresponsiveness in asthma 920 Dutch ancestry cases, 980 Dutch ancestry controls 2,589 European ancestry cases, 473 cases, 6,702 European ancestry controls, 1,892 controls Illumina [294932] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003589 Genome-wide genotyping array 2017-08-03 27132594 Mbarek H 2016-05-05 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27132594 Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility. Spontaneous dizygotic twinning 1,980 European ancestry mothers of spontaneous dizygotic twins, 12,953 European ancestry controls 3,597 Icelandic ancestry mothers of spontaneous dizygotic twins, 297,348 Icelandic ancestry controls Affymetrix, Illumina, Perlegen [at least 7903594] (imputed) 3 positive regulation of ovulation http://purl.obolibrary.org/obo/GO_0060279 GCST004413 Genome-wide genotyping array 2017-09-18 28739605 Zhou Y 2017-07-24 J Neurol Neurosurg Psychiatry www.ncbi.nlm.nih.gov/pubmed/28739605 Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis. Relapse in multiple sclerosis 268 cases 181 cases Illumina [1033813] (imputed) 1 disease recurrence http://www.ebi.ac.uk/efo/EFO_0004952 GCST004752 Genome-wide genotyping array 2017-08-09 28540843 Mbarek H 2017-05-25 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/28540843 Genome-Wide Significance for PCLO as a Gene for Major Depressive Disorder. Major depressive disorder 1,942 European ancestry cases, 4,565 European ancestry controls NA Affymetrix [NR] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST004486 Genome-wide genotyping array 2017-07-17 28500057 Bluett J 2017-05-12 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/28500057 HLA-A 31:01 is not associated with the development of methotrexate pneumonitis in the UK population: results from a genome-wide association study. Methotrexate-induced interstitial lung disease in rheumatoid arthritis 62 European ancestry cases, 175 European ancestry controls NA Illumina [NR] 3 response to methotrexate, interstitial lung disease http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004244 GCST004358 Genome-wide genotyping array 2018-02-27 29327327 Lin X 2018-01-11 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/29327327 Identifying potentially common genes between dyslipidemia and osteoporosis using novel analytical approaches. Femoral neck bone mineral density or plasma lipids (pleiotropy) 49,988 European and unknown ancestry individuals with femoral neck bone mineral density measurements, 188,577 European and unknown ancestry individuals with plasma lipid measurements NA NR [~ 2000000] (imputed) 0 lipid measurement, femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0007785 GCST005317 Genome-wide genotyping array 2018-09-07 27618448 Liu C 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618448 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Systolic blood pressure 120,473 European ancestry individuals, 21,503 African American individuals, 4,586 Hispanic individuals 154,543 European ancestry individuals, 26,183 South Asian ancestry individuals Illumina [247039] 17 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST006228 Exome genotyping array [Exome array] 2018-09-07 27618448 Liu C 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618448 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Mean arterial pressure 120,473 European ancestry individuals, 21,503 African American individuals, 4,586 Hispanic individuals NA Illumina [247039] 66 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST006231 Exome genotyping array [Exome array] 2018-09-07 27618448 Liu C 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618448 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Diastolic blood pressure 120,473 European ancestry individuals, 21,503 African American individuals, 4,586 Hispanic individuals 154,543 European ancestry individuals, 26,183 South Asian ancestry individuals Illumina [247039] 17 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST006227 Exome genotyping array [Exome array] 2018-09-07 27618448 Liu C 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618448 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Pulse pressure 120,473 European ancestry individuals, 21,503 African American individuals, 4,586 Hispanic individuals 154,543 European ancestry individuals, 26,183 South Asian ancestry individuals Illumina [247039] 11 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST006230 Exome genotyping array [Exome array] 2018-09-07 27618448 Liu C 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618448 Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci. Hypertension 120,473 European ancestry individuals, 21,503 African American individuals, 4,586 Hispanic individuals 154,543 European ancestry individuals, 26,183 South Asian ancestry individuals Illumina [247039] 5 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST006229 Exome genotyping array [Exome array] 2018-03-01 29331962 Kochi Y 2018-01-13 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29331962 Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis. Idiopathic inflammatory myopathy 576 Japanese ancestry cases, 6,270 East Asian controls NA Illumina [496819] 0 myositis http://www.ebi.ac.uk/efo/EFO_0000783 GCST005341 Genome-wide genotyping array 2018-03-01 29331962 Kochi Y 2018-01-13 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29331962 Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis. Polymyositis 236 Japanese ancestry cases, 6,270 East Asian ancestry controls NA Illumina [496819] 0 polymyositis http://www.ebi.ac.uk/efo/EFO_0003063 GCST005340 Genome-wide genotyping array 2018-03-01 29331962 Kochi Y 2018-01-13 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29331962 Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis. Dermatomyositis 340 Japanese ancestry cases, 6,270 East Asian ancestry controls NA Illumina [496819] 0 dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000398 GCST005339 Genome-wide genotyping array 2018-03-01 29331962 Kochi Y 2018-01-13 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29331962 Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis. Clinically amyopathic dermatomyositis 33 Japanese ancestry cases, 6,270 East Asian ancestry controls 21 European ancestry cases, 84 European ancestry controls Illumina [496819] 1 clinically amyopathic dermatomyositis http://www.ebi.ac.uk/efo/EFO_0008532 GCST005338 Genome-wide genotyping array 2018-03-01 29317604 Liu D 2018-01-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29317604 Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics. Plasma kynurenine levels in major depressive disorder 290 European ancestry individuals NA Illumina [~ 7500000] (imputed) 7 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST005342 Genome-wide genotyping array 2018-03-01 29317604 Liu D 2018-01-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29317604 Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics. Plasma kynurenine to tryptophan ratio in major depressive disorder 290 European ancestry individuals NA Illumina [~ 7500000] (imputed) 3 kynurenine:tryptophan ratio http://www.ebi.ac.uk/efo/EFO_0008530 GCST005343 Genome-wide genotyping array 2018-02-27 29367735 Nakagawa-Senda H 2018-01-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29367735 A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study. Coffee consumption 6,312 Japanese ancestry individuals 4,949 Japanese ancestry individuals Illumina [7094228] (imputed) 1 cups of coffee per day measurement http://www.ebi.ac.uk/efo/EFO_0006782 GCST005329 Genome-wide genotyping array 2018-02-27 29367735 Nakagawa-Senda H 2018-01-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29367735 A genome-wide association study in the Japanese population identifies the 12q24 locus for habitual coffee consumption: The J-MICC Study. Coffee consumption 11,261 Japanese ancestry individuals NA Illumina [7094228] (imputed) 4 cups of coffee per day measurement http://www.ebi.ac.uk/efo/EFO_0006782 GCST005330 Genome-wide genotyping array 2018-09-06 29315502 Tamraz B 2018-01-09 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/29315502 A Genome-Wide Association Study Identifies a Candidate Gene Associated With Atazanavir Exposure Measured in Hair. Atazanavir levels 64 European ancestry women, 194 African American women, 130 Hispanic women, 10 women 79 women Illumina [~ 14000000] (imputed) 1 atazanavir measurement http://www.ebi.ac.uk/efo/EFO_0009306 GCST006203 Genome-wide genotyping array 2017-09-11 28641744 Guo W 2017-07-01 Eur Neuropsychopharmacol www.ncbi.nlm.nih.gov/pubmed/28641744 Polygenic risk score and heritability estimates reveals a genetic relationship between ASD and OCD. Obsessive-compulsive disorder or autism spectrum disorder 2,998 European ancestry obsessive-compulsive disorder cases, 6,898 European ancestry autism spectrum disorder cases NA Illumina [6995140] (imputed) 13 obsessive-compulsive disorder, autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0003756 GCST004703 Genome-wide genotyping array 2017-09-11 28642124 Hensman Moss DJ 2017-06-20 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/28642124 Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study. Huntington's disease progression 1,989 European and unknown ancestry mutation carriers NA Illumina [9650000] (imputed) 20 Huntington disease, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0007739, http://www.ebi.ac.uk/efo/EFO_0008336 GCST004691 Genome-wide genotyping array 2017-09-28 28680059 Song X 2017-07-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28680059 GWAS follow-up study of esophageal squamous cell carcinoma identifies potential genetic loci associated with family history of upper gastrointestinal cancer. Family history of upper gastrointestinal cancer in esophageal squamous cell carcinoma 1,034 East Asian ancestry cases with family history of upper gastrointestinal cancer, 2,268 East Asian ancestry cases without family history of upper gastrointestinal cancer up to 2,801 East Asian ancestry cases with family history of upper gastrointestinal cancer, 3,136 East Asian ancestry cases without family history of upper gastrointestinal cancer NR [NR] (imputed) 0 family history of upper gastrointestinal cancer http://www.ebi.ac.uk/efo/EFO_0008346 GCST004799 Genome-wide genotyping array 2018-04-27 26651848 Rivera NV 2016-05-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26651848 High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences. Sarcoidosis (non-Lofgren's syndrome) 568 Swedish ancestry cases, 2,025 Swedish ancestry controls 763 European ancestry cases, 4,901 European ancestry controls, 781 African American ancestry cases, 876 African American ancestry controls Illumina [118177] 1 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST005543 Targeted genotyping array [ImmunoChip] 2018-04-27 26651848 Rivera NV 2016-05-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26651848 High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences. Sarcoidosis (non-Lofgren's syndrome without extrapulmonary manifestations) 451 Swedish ancestry cases, 2,086 Swedish ancestry controls NA Illumina [118177] 5 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST005542 Targeted genotyping array [ImmunoChip] 2018-04-27 26651848 Rivera NV 2016-05-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26651848 High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences. Sarcoidosis (Lofgren's syndrome vs non-Lofgren's syndrome) 664 Swedish ancestry non-Lofgren's syndrome cases, 384 Swedish ancestry Lofgren's syndrome cases 413 German ancestry non-Lofgren's syndrome cases, 64 German ancestry Lofgren's syndrome cases Illumina [118177] 25 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST005541 Targeted genotyping array [ImmunoChip] 2018-04-27 26651848 Rivera NV 2016-05-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26651848 High-Density Genetic Mapping Identifies New Susceptibility Variants in Sarcoidosis Phenotypes and Shows Genomic-driven Phenotypic Differences. Sarcoidosis (Lofgren's syndrome) 345 Swedish ancestry cases, 2,025 Swedish ancestry controls 251 European ancestry cases, 4,901 European ancestry controls Illumina [118177] 1 Löfgren’s syndrome http://www.ebi.ac.uk/efo/EFO_0009466 GCST005540 Targeted genotyping array [ImmunoChip] 2017-09-15 28654678 Mandage R 2017-06-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/28654678 Genetic factors affecting EBV copy number in lymphoblastoid cell lines derived from the 1000 Genome Project samples. Epstein-Barr virus copy number in lymphoblastoid cell lines 389 East Asian ancestry individuals, 189 South Asian ancestry individuals, 492 European ancestry individuals, 467 Sub-Saharan African ancestry individuals, 59 African American individuals, 157 Hispanic/Latino individuals NA NR [at least 880000] 42 Epstein-Barr virus infection http://www.ebi.ac.uk/efo/EFO_0000769 GCST004735 Genome-wide genotyping array 2017-11-27 29030599 Joshi PK 2017-10-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29030599 Genome-wide meta-analysis associates HLA-DQA1/DRB1 and LPA and lifestyle factors with human longevity. Parental lifespan up to 586,626 European ancestry individuals, up to 19,433 African ancestry individuals NA Affymetrix, Illumina [at least 13643373] (imputed) 5 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST004983 Genome-wide genotyping array 2017-09-18 28698626 Lopez-Mejias R 2017-07-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28698626 A genome-wide association study suggests the HLA Class II region as the major susceptibility locus for IgA vasculitis. Immunoglobulin A vasculitis 285 European ancestry cases, 1,006 European ancestry controls NA Illumina [1909910] (imputed) 7 Henoch-Schoenlein purpura http://www.ebi.ac.uk/efo/EFO_1000965 GCST004745 Genome-wide genotyping array 2018-04-25 23459209 Faraco J 2013-01-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23459209 ImmunoChip study implicates antigen presentation to T cells in narcolepsy. Narcolepsy 1,886 European ancestry cases, 10,421 European ancestry controls NA Illumina [111240] 8 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST005522 Targeted genotyping array [ImmunoChip] 2017-09-14 28651948 Peng C 2017-06-23 Bone www.ncbi.nlm.nih.gov/pubmed/28651948 Genetic sharing with coronary artery disease identifies potential novel loci for bone mineral density. Lumbar spine bone mineral density or coronary artery disease (pleiotropy) 53,236 individuals with bone mineral density measurements, 22,233 coronary artery disease cases, 64,762 controls NA NR [128164] (imputed) 0 spine bone mineral density, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0007701, http://www.ebi.ac.uk/efo/EFO_0001645 GCST004717 Genome-wide genotyping array 2018-11-08 24342994 Lencz T 2014-02-01 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24342994 Molecular genetic evidence for overlap between general cognitive ability and risk for schizophrenia: a report from the Cognitive Genomics consorTium (COGENT). General cognitive ability 4,896 European ancestry individuals NR Affymetrix, Illumina [up to 1078289] (imputed) 7 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST006523 Genome-wide genotyping array 2017-09-29 28808816 Xu C 2017-08-14 Biogerontology www.ncbi.nlm.nih.gov/pubmed/28808816 A genome-wide association study of cognitive function in Chinese adult twins. Cognitive function 139 Chinese ancestry dizygotic twin pairs NA Illumina [1048575] 12 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST004823 Genome-wide genotyping array 2017-03-28 27612410 van der Plaat DA 2016-09-06 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/27612410 Genome-wide association study on the FEV1/FVC ratio in never-smokers identifies HHIP and FAM13A. Pre bronchodilator FEV1/FVC ratio in never-smokers 5,070 European ancestry individuals 1,966 European ancestry individuals Illumina [227981] 3 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST003826 Genome-wide genotyping array 2018-01-18 29213071 Mendez-Giraldez R 2017-12-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29213071 GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals. QT interval 15,997 Hispanic/Latino individuals NA Affymetrix, Illumina [up to 17586686] (imputed) 62 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST005171 Genome-wide genotyping array 2017-01-12 27445529 Berube JC 2016-05-04 Can Respir J www.ncbi.nlm.nih.gov/pubmed/27445529 Identification of Susceptibility Genes of Adult Asthma in French Canadian Women. Asthma 240 French Canadian ancestry cases, 120 French Canadian ancestry controls 342 French Canadian ancestry cases, 213 European ancestry cases, 261 French Canadian ancestry controls, 142 European ancestry controls Illumina [730525] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003521 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Apolipoprotein B levels 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 5 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST005442 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Ratio of apolipoprotein A1 to apolipoprotein B 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 4 apolipoprotein A 1 measurement, apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004614, http://www.ebi.ac.uk/efo/EFO_0004615 GCST005443 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Esterified cholesterol levels 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 7 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST005444 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 7 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST005445 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 37 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005446 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 53 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005447 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Serum total cholesterol levels 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 58 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST005448 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total triglycerides levels 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 54 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005449 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Mean diameter of HDL particles 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 17 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST005455 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Mean diameter of LDL particles 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 12 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST005456 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Mean diameter of VLDL particles 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 1 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST005457 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Very large VLDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005450 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in very large VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 2 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005451 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in very large VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005452 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Very large VLDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 21 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005453 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in large VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 18 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005454 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in large VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005458 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in large VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST005459 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in large VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 20 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005460 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Cholesterol ester levels in large VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST005461 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Medium VLDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 24 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005462 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in medium VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 24 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005463 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in medium VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 19 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005464 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Cholesterol ester levels in medium VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 2 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST005465 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in medium VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 22 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST005466 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in medium VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 26 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005467 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Small VLDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 25 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005468 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in small VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 24 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005469 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in small VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 1 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005470 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in small VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 1 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST005471 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in small VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 30 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005472 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Very small VLDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST005473 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in very small VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 3 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005474 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in very small VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005475 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. IDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 1 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST005476 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in IDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 phospholipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0008595 GCST005477 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. IDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 8 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST005478 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in IDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 9 free cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008595 GCST005479 Genome-wide genotyping array 2018-04-10 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in IDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 10 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005480 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Large LDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005481 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in large LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005482 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in large LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 8 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005483 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Cholesterol ester levels in large LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 6 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST005484 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in large LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 12 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST005485 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Medium LDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 8 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005486 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in medium LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 1 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005487 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in medium LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 8 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005488 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Cholesterol ester levels in medium LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 9 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST005489 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Small LDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 26 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005490 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in small LDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 22 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST005491 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Very large HDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005492 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in very large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005493 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in very large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005494 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Cholesterol ester levels in very large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 0 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005495 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in very large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 2 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005496 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in very large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 19 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005498 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Large HDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 15 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005497 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 19 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005499 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005500 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Cholesterol ester levels in very large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 3 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005501 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in large HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 5 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005502 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Medium HDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 11 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005503 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in medium HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 17 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005504 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Total cholesterol levels in medium HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 5 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005505 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Cholesterol ester levels in medium HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 5 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST005506 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Free cholesterol levels in medium HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 6 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005507 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Small HDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005508 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in small HDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005509 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Chylomicron and largest VLDL particle concentration 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 2 chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST005510 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Phospholipid levels in chylomicrons and largest VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST005511 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Triglyceride levels in chylomicrons and largest VLDL 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005512 Genome-wide genotyping array 2018-04-12 29084231 Davis JP 2017-10-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29084231 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. Apolipoprotein A1 levels 8,372 Finnish ancestry males NA Illumina [15144991] (imputed) 12 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST005513 Genome-wide genotyping array 2016-12-16 27142678 Amin N 2016-05-04 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27142678 Genetic variants in RBFOX3 are associated with sleep latency. Sleep latency 1983 European ancestry individuals, 747 Erasmus Rucphen (founder/genetic isolate) individuals, 610 Korculan (founder/genetic isolate) individuals, 696 Tyrolean (founder/genetic isolate) individuals, 206 Orcadian (founder/genetic isolate) individuals 30,377 European ancestry individuals Affymetrix, Illumina, Perlegen [2572737] (imputed) 1 sleep latency http://www.ebi.ac.uk/efo/EFO_0005280 GCST003481 Genome-wide genotyping array 2017-01-16 27149122 Smith JG 2016-05-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27149122 Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure. Mortality in heart failure 1798 European ancestry cases, 1030 European ancestry controls 889 European ancestry cases, 981 European ancestry controls Affymetrix, Illumina [2500000] (imputed) 2 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST003539 Genome-wide genotyping array 2016-12-16 27142222 White MJ 2016-05-03 Immunogenetics www.ncbi.nlm.nih.gov/pubmed/27142222 Novel genetic risk factors for asthma in African American children: Precision Medicine and the SAGE II Study. Asthma (childhood onset) 812 African American child cases, 415 African American child controls NA Affymetrix [797128] 3 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST003482 Genome-wide genotyping array 2018-03-12 29207912 Nishizawa D 2017-12-06 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/29207912 Genome-wide scan identifies candidate loci related to remifentanil requirements during laparoscopic-assisted colectomy. Opioid requirements during laparoscopic-assisted colectomy 117 Japanese ancestry patients 234 Japanese ancestry patients Illumina [921239] 2 response to opioid, analgesia requirement measurement http://www.ebi.ac.uk/efo/EFO_0008541, http://www.ebi.ac.uk/efo/EFO_0008544 GCST005364 Genome-wide genotyping array 2017-03-31 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity and pharyngeal cancer 2,717 European ancestry oral cavity cancer cases, 273 oral cavity cancer cases, 2,506 European ancestry oropharynx cancer cases, 135 oropharynx cancer cases, 305 European and unknown ancestry hypopharynx cancer cases, 73 European and unknown ancestry overlapping cases, 25 European and unknown ancestry cases, 5,984 European ancestry controls, 601 controls NA Illumina [7574753] (imputed) 5 head and neck malignant neoplasia http://www.ebi.ac.uk/efo/EFO_0006859 GCST003857 Genome-wide genotyping array 2017-03-31 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oropharynx cancer 2,506 European ancestry cases, 135 cases, 5,984 European ancestry controls, 601 controls NA Illumina [7574753] (imputed) 17 oropharynx cancer http://www.ebi.ac.uk/efo/EFO_1001931 GCST003859 Genome-wide genotyping array 2017-03-31 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity cancer 2,717 European ancestry cases, 273 cases, 5,984 European ancestry controls, 601 controls NA Illumina [7574753] (imputed) 9 oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0005570 GCST003858 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity and pharyngeal cancer 2,342 European ancestry cases, 2,329 European ancestry controls NA Illumina [7574753] (imputed) 0 head and neck malignant neoplasia http://www.ebi.ac.uk/efo/EFO_0006859 GCST012234 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity and pharyngeal cancer 2,497 European ancestry cases, 2,928 European ancestry controls NA Illumina [7574753] (imputed) 0 head and neck malignant neoplasia http://www.ebi.ac.uk/efo/EFO_0006859 GCST012235 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity and pharyngeal cancer 613 Hispanic or Latin American ancestry cases, 727 Hispanic or Latin American ancestry controls NA Illumina [7574753] (imputed) 0 head and neck malignant neoplasia http://www.ebi.ac.uk/efo/EFO_0006859 GCST012236 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity cancer 1,223 European ancestry cases, 2,928 European ancestry controls NA Illumina [7574753] (imputed) 0 oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0005570 GCST012237 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity cancer 1,135 European ancestry cases, 2,329 European ancestry controls NA Illumina [7574753] (imputed) 0 oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0005570 GCST012238 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oral cavity cancer 340 Hispanic or Latin American ancestry cases, 727 Hispanic or Latin American ancestry controls NA Illumina [7574753] (imputed) 0 oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0005570 GCST012239 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oropharynx cancer 1,090 European ancestry cases, 2,928 European ancestry controls NA Illumina [7574753] (imputed) 0 oropharynx cancer http://www.ebi.ac.uk/efo/EFO_1001931 GCST012241 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oropharynx cancer 1,119 European ancestry cases, 2,329 European ancestry controls NA Illumina [7574753] (imputed) 0 oropharynx cancer http://www.ebi.ac.uk/efo/EFO_1001931 GCST012242 Genome-wide genotyping array 2021-08-25 27749845 Lesseur C 2016-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27749845 Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer. Oropharynx cancer 205 Hispanic or Latin American ancestry cases, 727 Hispanic or Latin American ancestry controls NA Illumina [7574753] (imputed) 0 oropharynx cancer http://www.ebi.ac.uk/efo/EFO_1001931 GCST012240 Genome-wide genotyping array 2017-02-10 26202629 Johnson EO 2016-07-23 Addict Biol www.ncbi.nlm.nih.gov/pubmed/26202629 KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. Drug abuse 2,017 African American ancestry cases, 1,142 European ancestry cases,1,725 African American ancestry controls, 5,703 European ancestry controls 259 African American ancestry cases, 273 European ancestry cases, 496 African American ancestry controls, 858 European ancestry controls Illumina [at least 6727359] (imputed) 1 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST003601 Genome-wide genotyping array 2017-03-17 27764096 Hoffmann TJ 2016-10-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27764096 A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records. Age-related hearing impairment 6,527 European ancestry cases, 45,882 European ancestry controls 481 Latino cases, 398 East Asian ancestry cases, 146 African American cases, 5,215 Latino controls, 5,040 East Asian ancestry controls, 2,133 African American controls Affymetrix [9469183] (imputed) 3 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST003763 Genome-wide genotyping array 2017-03-14 27769005 Nassan M 2016-09-30 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/27769005 A genome wide association study suggests the association of muskelin with early onset bipolar disorder: Implications for a GABAergic epileptogenic neurogenesis model. Bipolar disorder (early onset) 600 European ancestry cases, 1,811 European ancestry controls 142 European ancestry cases, 746 European ancestry controls Affymetrix, Illumina [7859701] (imputed) 1 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST003742 Genome-wide genotyping array 2017-04-01 27764105 Lemmela S 2016-10-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/27764105 Genome-Wide Meta-Analysis of Sciatica in Finnish Population. Sciatica 291 Finnish (founder/genetic isolate) cases, 3,671 Finnish (founder/genetic isolate) controls 776 Finnish (founder/genetic isolate) cases, 18,489 Finnish (founder/genetic isolate) controls Illumina [~ 7700000] (imputed) 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST003869 Genome-wide genotyping array 2018-09-20 28869591 Kemp JP 2017-09-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28869591 Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis. Heel bone mineral density 76,067 European ancestry women, 66,420 European ancestry men NA NR [17166351] (imputed) 766 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST006288 Genome-wide genotyping array 2017-04-01 27723779 Gong J 2016-10-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27723779 Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer. Colorectal cancer (alcohol consumption interaction) 8,058 European ancestry non/occasional, light-to-moderate, and heavy drinker cases, 8,765 European ancestry non/occasional, light-to-moderate, and heavy drinker controls NA Affymetrix, Illumina [~ 2700000] (imputed) 2 colorectal cancer, alcohol consumption measurement http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0007878 GCST003873 Genome-wide genotyping array 2017-04-01 27723779 Gong J 2016-10-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27723779 Genome-Wide Interaction Analyses between Genetic Variants and Alcohol Consumption and Smoking for Risk of Colorectal Cancer. Colorectal cancer (smoking interaction) 11,219 European ancestry ever-smoker and never-smoker cases, 11,382 European ancestry ever-smoker and never-smoker controls NA Affymetrix, Illumina [~ 2700000] (imputed) 0 smoking status measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0006527, http://purl.obolibrary.org/obo/MONDO_0005575 GCST003874 Genome-wide genotyping array 2017-01-12 27153935 Zhang CE 2016-05-06 J Dermatol www.ncbi.nlm.nih.gov/pubmed/27153935 Variation at HLA-DPB1 is associated with dermatomyositis in Chinese population. Dermatomyositis 127 Han Chinese ancestry case, 1,566 Han Chinese ancestry controls NA Illumina [812602] 4 dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000398 GCST003522 Genome-wide genotyping array 2017-03-27 27696742 Yau MS 2016-10-01 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/27696742 Genome-Wide Association Study of Radiographic Knee Osteoarthritis in North American Caucasians. Knee osteoarthritis 2,672 European ancestry cases, 1,776 European ancestry controls 1,226 European ancestry cases, 1,392 European ancestry controls Illumina [at least 8248570] (imputed) 6 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST003820 Genome-wide genotyping array 2017-03-28 27723809 Matsunami K 2016-10-10 PLoS One www.ncbi.nlm.nih.gov/pubmed/27723809 Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C. Depression in response to interferon-based therapy in chronic hepatitis C 45 Japanese ancestry cases, 179 Japanese ancestry controls 40 Japanese ancestry cases, 120 Japanese ancestry controls Affymetrix [at least 551176] (imputed) 4 response to interferon, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007859, http://www.ebi.ac.uk/efo/EFO_0007006 GCST003824 Genome-wide genotyping array 2018-02-06 26284813 Hayes MG 2015-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26284813 Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Luteinizing hormone levels in polycystic ovary syndrome 645 European ancestry cases 607 European ancestry cases Illumina [at least 624044] (imputed) 3 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST005269 Genome-wide genotyping array 2018-02-06 26284813 Hayes MG 2015-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26284813 Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Follicle stimulating hormone levels in polycystic ovary syndrome 647 European ancestry cases 606 European ancestry cases Illumina [at least 624044] (imputed) 4 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST005270 Genome-wide genotyping array 2018-02-06 26284813 Hayes MG 2015-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26284813 Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Sex hormone-binding globulin levels in polycystic ovary syndrome 903 European ancestry cases 1,156 European ancestry cases Illumina [at least 624044] (imputed) 1 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST005271 Genome-wide genotyping array 2018-02-06 26284813 Hayes MG 2015-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26284813 Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Testosterone levels in polycystic ovary syndrome 957 European ancestry cases 1,516 European ancestry cases Illumina [at least 624044] (imputed) 4 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST005272 Genome-wide genotyping array 2018-02-06 26284813 Hayes MG 2015-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26284813 Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. Polycystic ovary syndrome 984 European ancestry cases, 2,964 European ancestry controls 2,021 European ancestry cases, 2,566 European ancestry controls Illumina [at least 624044] (imputed) 7 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST005273 Genome-wide genotyping array 2018-02-06 26284813 Hayes MG 2015-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26284813 Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations. DHEAS levels in polycystic ovary syndrome up to 984 European ancestry cases up to 2,021 European ancestry cases Illumina [at least 624044] (imputed) 0 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST005274 Genome-wide genotyping array 2018-07-03 29356057 Du Z 2018-01-21 Prostate www.ncbi.nlm.nih.gov/pubmed/29356057 Genetic risk of prostate cancer in Ugandan men. Prostate cancer 560 Ugandan ancestry cases, 480 Ugandan ancestry controls NA Illumina [17125421] (imputed) 25 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST005786 Genome-wide genotyping array 2018-03-12 29324852 Primes G 2018-01-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/29324852 Real-life helping behaviours in North America: A genome-wide association approach. Helping behaviour (self reported) 10,713 European ancestry, African American and unknown ancestry individuals NA Illumina [1224134] (imputed) 7 helping behavior measurement http://www.ebi.ac.uk/efo/EFO_0008538 GCST005355 Genome-wide genotyping array 2018-01-18 29235454 Choquet H 2017-12-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29235454 A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure. Intraocular pressure 56,819 European ancestry individuals, 5,748 Hispanic/Latino individuals, 5,119 East Asian ancestry individuals, 2,070 African American individuals 37,930 European and Asian ancestry individuals Affymetrix [at least 665000] (imputed) 56 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST005170 Genome-wide genotyping array 2017-09-18 25676789 Wen CC 2015-05-01 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/25676789 Genome-wide association study identifies ABCG2 (BCRP) as an allopurinol transporter and a determinant of drug response. Serum uric acid levels in response to allopurinol in gout 1,607 European ancestry individuals, 238 East Asian individuals, 84 African American individuals, 85 Hispanic individuals, 13 individuals NA Affymetrix [NR] (imputed) 26 response to allopurinol, uric acid measurement http://www.ebi.ac.uk/efo/EFO_0006337, http://www.ebi.ac.uk/efo/EFO_0004761 GCST004751 Genome-wide genotyping array 2017-08-17 28649644 Pivot X 2017-02-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/28649644 Constitutional variants are not associated with HER2-positive breast cancer: results from the SIGNAL/PHARE clinical cohort. HER2 status in breast cancer 5,473 European ancestry HER2-negative cases, 3,230 European ancestry HER2-positive cases NA Illumina [914144] (imputed) 1 HER2 status http://www.ebi.ac.uk/efo/EFO_0005514 GCST004528 Genome-wide genotyping array 2017-09-16 28703135 Ruamviboonsuk P 2017-07-13 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28703135 Genome-wide association study of neovascular age-related macular degeneration in the Thai population. Neovascular age-related macular degeneration 377 Thai ancestry cases, 1,074 Thai ancestry controls 222 Thai ancestry cases, 623 Thai ancestry controls Illumina [958497] 4 age-related macular degeneration, wet macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365, http://www.ebi.ac.uk/efo/EFO_0004683 GCST004737 Genome-wide genotyping array 2017-10-05 28869801 Takahashi Y 2017-09-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/28869801 Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14. Colorectal cancer 529 Japanese ancestry cases, 521 Japanese ancestry controls 1,269 Japanese ancestry cases, 2,104 Japanese ancestry controls Affymetrix [280972] 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST004839 Genome-wide genotyping array 2017-10-05 28869801 Takahashi Y 2017-09-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/28869801 Japanese genome-wide association study identifies a significant colorectal cancer susceptibility locus at chromosome 10p14. Colorectal cancer 529 Japanese ancestry cases, 521 Japanese ancestry controls 1,181 Japanese ancestry cases, 1,617 Japanese ancestry controls Affymetrix [280972] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST004840 Genome-wide genotyping array 2018-01-12 28800628 Salem JE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800628 GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Sotalol-induced IKr potassium channel inhibition (T wave peak and end interval change) 448 European ancestry individuals, 47 North African ancestry individuals 431 European ancestry individuals, 64 North African ancestry individuals Illumina [8306856] (imputed) 0 response to sotalol, TpTe measurement http://www.ebi.ac.uk/efo/EFO_0008325, http://www.ebi.ac.uk/efo/EFO_0008334 GCST005134 Genome-wide genotyping array 2018-01-12 28800628 Salem JE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800628 GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Sotalol-induced IKr potassium channel inhibition (T wave maximal amplitude change) 448 European ancestry individuals, 47 North African ancestry individuals 431 European ancestry individuals, 64 North African ancestry individuals Illumina [8306856] (imputed) 0 response to sotalol, T wave amplitude http://www.ebi.ac.uk/efo/EFO_0008325, http://www.ebi.ac.uk/efo/EFO_0008333 GCST005135 Genome-wide genotyping array 2018-01-12 28800628 Salem JE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800628 GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Sotalol-induced IKr potassium channel inhibition (ventricular repolarization duration change) 448 European ancestry individuals, 47 North African ancestry individuals 431 European ancestry individuals, 64 North African ancestry individuals Illumina [8306856] (imputed) 0 response to sotalol, ventricular repolarisation duration measurement http://www.ebi.ac.uk/efo/EFO_0008325, http://www.ebi.ac.uk/efo/EFO_0008335 GCST005140 Genome-wide genotyping array 2018-01-12 28800628 Salem JE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800628 GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Sotalol-induced IKr potassium channel inhibition (ventricular repolarization changes PC2) 448 European ancestry individuals, 47 North African ancestry individuals 431 European ancestry individuals, 64 North African ancestry individuals Illumina [8306856] (imputed) 0 response to sotalol, T wave amplitude, TpTe measurement, ventricular repolarisation duration measurement http://www.ebi.ac.uk/efo/EFO_0008325, http://www.ebi.ac.uk/efo/EFO_0008333, http://www.ebi.ac.uk/efo/EFO_0008334, http://www.ebi.ac.uk/efo/EFO_0008335 GCST005136 Genome-wide genotyping array 2018-01-12 28800628 Salem JE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800628 GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Sotalol-induced IKr potassium channel inhibition (ventricular repolarization changes PC3) 448 European ancestry individuals, 47 North African ancestry individuals 431 European ancestry individuals, 64 North African ancestry individuals Illumina [8306856] (imputed) 0 response to sotalol, T wave amplitude, TpTe measurement, ventricular repolarisation duration measurement http://www.ebi.ac.uk/efo/EFO_0008325, http://www.ebi.ac.uk/efo/EFO_0008333, http://www.ebi.ac.uk/efo/EFO_0008334, http://www.ebi.ac.uk/efo/EFO_0008335 GCST005138 Genome-wide genotyping array 2018-01-12 28800628 Salem JE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800628 GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Sotalol-induced IKr potassium channel inhibition (ventricular repolarization changes PC1) 448 European ancestry individuals, 47 North African ancestry individuals 431 European ancestry individuals, 64 North African ancestry individuals Illumina [8306856] (imputed) 0 response to sotalol, T wave amplitude, TpTe measurement, ventricular repolarisation duration measurement http://www.ebi.ac.uk/efo/EFO_0008325, http://www.ebi.ac.uk/efo/EFO_0008333, http://www.ebi.ac.uk/efo/EFO_0008334, http://www.ebi.ac.uk/efo/EFO_0008335 GCST005139 Genome-wide genotyping array 2018-01-12 28800628 Salem JE 2017-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/28800628 GENomE wide analysis of sotalol-induced IKr inhibition during ventricular REPOLarization, "GENEREPOL study": Lack of common variants with large effect sizes. Sotalol-induced IKr potassium channel inhibition (T wave morphology notching) 448 European ancestry individuals, 47 North African ancestry individuals 431 European ancestry individuals, 64 North African ancestry individuals Illumina [8306856] (imputed) 0 response to sotalol, T wave morphology measurement http://www.ebi.ac.uk/efo/EFO_0008325, http://www.ebi.ac.uk/efo/EFO_0008398 GCST005137 Genome-wide genotyping array 2018-01-26 29212897 Salminen A 2017-12-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/29212897 Genetic Variants Contributing to Circulating Matrix Metalloproteinase 8 Levels and Their Association With Cardiovascular Diseases: A Genome-Wide Analysis. Matrix metalloproteinase-8 levels 6,049 Finnish ancestry individuals NA Illumina [at least 2300000] (imputed) 2 matrix metalloproteinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0008466 GCST005187 Genome-wide genotyping array 2018-01-04 29209388 Cho CH 2017-11-07 Psychiatry Investig www.ncbi.nlm.nih.gov/pubmed/29209388 A Genome-Wide Association Study Identifies UTRN Gene Polymorphism for Restless Legs Syndrome in a Korean Population. Restless legs syndrome 325 Korean ancestry cases, 2,603 Korean ancestry controls 227 Korean ancestry cases, 229 Korean ancestry controls Affymetrix [1031877] (imputed) 0 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST005107 Genome-wide genotyping array 2017-10-20 28869590 Zhao W 2017-09-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28869590 Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. Type 2 diabetes 6,353 South Asian ancestry cases, 7,179 South Asian ancestry controls, 3,871 European ancestry cases, 16,427 European ancestry controls, 34,840 cases, 114,981 controls 7,888 South Asian ancestry cases, 20,679 South Asian ancestry controls, 387 European ancestry cases, 2,092 European ancestry controls, 19,998 East Asian ancestry cases, 30,983 East Asian ancestry controls Affymetrix, Illumina [NR] (imputed) 157 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004894 Genome-wide genotyping array 2017-09-11 27455348 van Rheenen W 2016-07-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27455348 Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 12,577 European ancestry cases, 23,475 European ancestry controls 2,579 European ancestry cases, 2,767 European ancestry controls Illumina [8697640] (imputed) 7 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST004692 Genome-wide genotyping array 2017-01-13 27149984 Degenhardt F 2016-05-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27149984 Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases. Coenzyme Q10 levels up to 1,300 European ancestry individuals NA Affymetrix, Illumina [up to 17017474] (imputed) 25 coenzyme Q10 measurement http://www.ebi.ac.uk/efo/EFO_0007836 GCST003523 Genome-wide genotyping array 2017-02-24 27143689 Hertz DL 2016-05-03 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/27143689 Pharmacogenetic Discovery in CALGB (Alliance) 90401 and Mechanistic Validation of a VAC14 Polymorphism that Increases Risk of Docetaxel-Induced Neuropathy. Docetaxel-induced peripheral neuropathy in metastatic castrate-resistant prostate cancer 50 European ancestry cases with neuropathy, 573 European ancestry cases without neuropathy NA Illumina [498081] 12 peripheral neuropathy, response to docetaxel trihydrate http://www.ebi.ac.uk/efo/EFO_0003100, http://purl.obolibrary.org/obo/GO_1902519 GCST003672 Genome-wide genotyping array 2017-04-21 27454463 Jones AV 2016-11-01 Pain www.ncbi.nlm.nih.gov/pubmed/27454463 Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus. Dysmenorrheic pain 1,785 European ancestry individuals with no pain, 3,478 European ancestry individuals with little pain, 4,208 European ancestry individuals with moderate pain, 2,420 European ancestry individuals with extreme pain NA Illumina [11942402] (imputed) 6 dysmenorrheic pain measurement http://www.ebi.ac.uk/efo/EFO_0007889 GCST003927 Genome-wide genotyping array 2017-04-01 28364478 Sulkava S 2016-10-10 Sleep www.ncbi.nlm.nih.gov/pubmed/28364478 Common Genetic Variation Near Melatonin Receptor 1A Gene Linked to Job-Related Exhaustion in Shift Workers. Job-related exhaustion in shift workers 176 Finnish ancestry individuals 577 Finnish ancestry individuals Illumina [NR] 1 job-related exhaustion measurement http://www.ebi.ac.uk/efo/EFO_0007881 GCST003868 Genome-wide genotyping array 2016-12-20 27106561 Cornelis MC 2016-04-23 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/27106561 A genome-wide investigation of food addiction. Food addiction up to 9,314 European ancestry individuals NA Affymetrix, Illumina [~ 31000000] (imputed) 11 eating behaviour, food addiction measurement http://www.ebi.ac.uk/efo/EFO_0007829, http://www.ebi.ac.uk/efo/EFO_0007830 GCST003489 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. B cell acute lymphoblastic leukaemia (normal cytogenetics) 193 European ancestry cases, 3027 European ancestry controls NA Illumina [~ 8500000] (imputed) 3 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005965 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. B cell acute lymphoblastic leukaemia (hyperdiploid negative) 410 European ancestry cases, 3027 European ancestry controls NA Illumina [~ 8500000] (imputed) 3 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005966 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. B cell acute lymphoblastic leukaemia (Philadelphia chromosome negative) 333 European ancestry cases, 3,027 European ancestry controls NA Illumina [~ 8500000] (imputed) 3 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005967 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. B cell acute lymphoblastic leukaemia (abnormal cytogenetics) 253 European ancestry cases, 3,027 European ancestry controls NA Illumina [~ 8500000] (imputed) 1 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005968 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. Acute lymphoblastic leukemia in childhood (B cell precursor) 134 European ancestry cases, 3,027 European ancestry controls NA Illumina [~ 8500000] (imputed) 1 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005969 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. B cell acute lymphoblastic leukaemia in young adulthood 160 European ancestry cases, 3,027 European ancestry controls NA Illumina [~ 8500000] (imputed) 1 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005970 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. B cell acute lymphoblastic leukaemia in adulthood 152 European ancestry cases, 3,027 European ancestry controls NA Illumina [~ 8500000] (imputed) 1 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005971 Genome-wide genotyping array 2018-07-25 29296818 Clay-Gilmour AI 2017-09-08 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296818 Genetic association with B-cell acute lymphoblastic leukemia in allogeneic transplant patients differs by age and sex. Acute lymphoblastic leukemia (B-cell precursor) 272 European ancestry male cases, 174 European ancestry female cases, 2,098 European ancestry male controls, 929 European ancestry female controls NA Illumina [~ 8500000] (imputed) 3 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005972 Genome-wide genotyping array 2018-02-23 29348612 Wiemels JL 2018-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29348612 GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. Acute lymphoblastic leukemia (childhood) 1,949 Latino cases, 8,584 Latino controls, 1,184 European ancestry cases, 3551 European ancestry controls, 130 African American cases, 3,842 African American controls 959 European ancestry cases, 2,624 European ancestry controls, 530 Latino cases, 511 Latino controls Affymetrix [757935] 9 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST005315 Genome-wide genotyping array 2018-03-29 29378355 Stanne TM 2018-02-01 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/29378355 A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor. Thrombin-activatable fibrinolysis inhibitor levels 3,116 European ancestry individuals NA Illumina [10000000] (imputed) 7 carboxypeptidase B2 measurement http://www.ebi.ac.uk/efo/EFO_0008069 GCST005412 Genome-wide genotyping array 2018-03-29 29378355 Stanne TM 2018-02-01 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/29378355 A Genome-wide Study of Common and Rare Genetic Variants Associated with Circulating Thrombin Activatable Fibrinolysis Inhibitor. Thrombin-activatable fibrinolysis inhibitor activation peptide 3,124 European ancestry individuals NA Illumina [10000000] (imputed) 11 thrombin activatable fibrinolysis inhibitor activation peptide measurement http://www.ebi.ac.uk/efo/EFO_0008582 GCST005411 Genome-wide genotyping array 2018-02-09 29354237 Kim HA 2018-01-01 J Korean Neurosurg Soc www.ncbi.nlm.nih.gov/pubmed/29354237 Novel Genetic Variants Associated with Lumbar Spondylosis in Koreans : A Genome-Wide Association Study. Lumbar spondylosis (disc space narrowing) 228 Korean ancestry cases, 1197 Korean ancestry controls NA Affymetrix [352228] 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST005279 Genome-wide genotyping array 2018-02-09 29354237 Kim HA 2018-01-01 J Korean Neurosurg Soc www.ncbi.nlm.nih.gov/pubmed/29354237 Novel Genetic Variants Associated with Lumbar Spondylosis in Koreans : A Genome-Wide Association Study. Lumbar spondylosis (presence and severity of osteophytes) 762 Korean ancestry cases, 664 Korean ancestry controls NA Affymetrix [352228] 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST005278 Genome-wide genotyping array 2018-02-09 29354237 Kim HA 2018-01-01 J Korean Neurosurg Soc www.ncbi.nlm.nih.gov/pubmed/29354237 Novel Genetic Variants Associated with Lumbar Spondylosis in Koreans : A Genome-Wide Association Study. Lumbar spondylosis (Kellgren-Lawrence grade) 1,029 Korean ancestry cases, 395 Korean ancestry controls NA Affymetrix [352228] 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST005277 Genome-wide genotyping array 2017-09-28 28714975 Nelson CP 2017-07-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28714975 Association analyses based on false discovery rate implicate new loci for coronary artery disease. Coronary artery disease (myocardial infarction, percutaneous transluminal coronary angioplasty, coronary artery bypass grafting, angina or chromic ischemic heart disease) 18,467 European and unknown ancestry cases, 45,264 European and unknown ancestry controls 57,347 European and unknown ancestry cases, 219,521 European and unknown ancestry controls Affymetrix [9149595] (imputed) 72 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST004787 Genome-wide genotyping array 2017-08-16 27500523 Zhou K 2016-09-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27500523 Variation in the glucose transporter gene SLC2A2 is associated with glycemic response to metformin. Response to metformin in type 2 diabetes (HbA1c reduction) 1,372 European ancestry individuals 9,184 European ancestry individuals, 1,196 African American ancestry individuals, 627 Asian American individuals, 743 Latino individuals NR [705124] 1 HbA1c measurement, response to metformin http://www.ebi.ac.uk/efo/EFO_0004541, http://purl.obolibrary.org/obo/GO_1901558 GCST004522 Genome-wide genotyping array 2017-03-30 27611488 Almoguera B 2016-09-09 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/27611488 Identification of Four Novel Loci in Asthma in European American and African American Populations. Adult asthma 337 African American allergic asthma cases, 321 African American non-allergic asthma cases, 1,367 African American controls, 466 European American allergic asthma cases, 626 European American non-allergic asthma cases, 7,878 European American controls NA Affymetrix, Illumina [NR] (imputed) 24 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003833 Genome-wide genotyping array 2017-03-30 27611488 Almoguera B 2016-09-09 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/27611488 Identification of Four Novel Loci in Asthma in European American and African American Populations. Asthma 819 African American non-allergic asthma cases, 2,218 African American allergic asthma cases 4,360 African American controls, 808 European American non-allergic asthma cases, 1,464 European American allergic asthma cases, 11,975 European American controls NA Affymetrix, Illumina [NR] (imputed) 49 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003831 Genome-wide genotyping array 2017-03-30 27611488 Almoguera B 2016-09-09 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/27611488 Identification of Four Novel Loci in Asthma in European American and African American Populations. Asthma (childhood onset) 1,181 African American allergic asthma child cases, 498 African American non-allergic asthma child cases, 2,993 African American child controls, 998 European American allergic asthma child cases, 182 European American non-allergic asthma child cases, 4,097 European American child controls. NA Affymetrix, Illumina [NR] (imputed) 27 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003832 Genome-wide genotyping array 2018-07-13 29212154 Lin E 2017-09-16 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29212154 Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population. Metabolic syndrome 1,811 Taiwanese Han Chinese ancestry cases, 8,489 Taiwanese Han Chinese ancestry controls NA Affymetrix [583469] 2 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST005871 Genome-wide genotyping array 2018-07-13 29212154 Lin E 2017-09-16 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29212154 Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population. Waist circumference 1,811 Taiwanese Han Chinese individuals with metabolic syndrome, 8,489 Taiwanese Han Chinese ancestry individuals without metabolic syndrome NA Affymetrix [583469] 1 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST005872 Genome-wide genotyping array 2018-07-13 29212154 Lin E 2017-09-16 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29212154 Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population. Triglyceride levels 1,811 Taiwanese Han Chinese individuals with metabolic syndrome, 8,489 Taiwanese Han Chinese ancestry individuals without metabolic syndrome NA Affymetrix [583469] 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005873 Genome-wide genotyping array 2018-07-13 29212154 Lin E 2017-09-16 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29212154 Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population. HDL cholesterol 1,811 Taiwanese Han Chinese individuals with metabolic syndrome, 8,489 Taiwanese Han Chinese ancestry individuals without metabolic syndrome NA Affymetrix [583469] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005874 Genome-wide genotyping array 2018-07-13 29212154 Lin E 2017-09-16 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29212154 Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population. Diastolic blood pressure 1,811 Taiwanese Han Chinese individuals with metabolic syndrome, 8,489 Taiwanese Han Chinese ancestry individuals without metabolic syndrome NA Affymetrix [583469] 1 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST005875 Genome-wide genotyping array 2018-07-13 29212154 Lin E 2017-09-16 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29212154 Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population. Systolic blood pressure 1,811 Taiwanese Han Chinese individuals with metabolic syndrome, 8,489 Taiwanese Han Chinese ancestry individuals without metabolic syndrome NA Affymetrix [583469] 1 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST005876 Genome-wide genotyping array 2018-07-13 29212154 Lin E 2017-09-16 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29212154 Detection of susceptibility loci on APOA5 and COLEC12 associated with metabolic syndrome using a genome-wide association study in a Taiwanese population. Fasting blood glucose 1,811 Taiwanese Han Chinese individuals with metabolic syndrome, 8,489 Taiwanese Han Chinese ancestry individuals without metabolic syndrome NA Affymetrix [583469] 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST005877 Genome-wide genotyping array 2017-02-17 27189021 Cook JP 2016-05-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27189021 Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibility. Type 2 diabetes 746 African American cases, 2,825 African American controls, 743 East Asian ancestry cases, 3,992 East Asian ancestry controls, 7,111 European ancestry cases, 49,688 European ancestry controls, 1,147 Latino cases, 5,352 Latino controls 12,171 European ancestry cases, 56,862 European ancestry controls NR [at least 8497425] (imputed) 10 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST003619 Genome-wide genotyping array 2017-01-16 27173062 Azad AK 2016-05-09 Cancer Epidemiol www.ncbi.nlm.nih.gov/pubmed/27173062 A genome-wide association study of non-HPV-related head and neck squamous cell carcinoma identifies prognostic genetic sequence variants in the MAP-kinase and hormone pathways. Survival in head and neck cancer 489 European ancestry cases, 26 Asian, African or First Nation ancestry cases 470 European ancestry cases, 57 Asian ancestry cases, 11 African American ancestry cases, 28 other ancestry cases Illumina [543873] 1 head and neck malignant neoplasia, survival time http://www.ebi.ac.uk/efo/EFO_0006859, http://www.ebi.ac.uk/efo/EFO_0000714 GCST003541 Genome-wide genotyping array 2016-12-16 26989097 Coleman JR 2016-03-17 Br J Psychiatry www.ncbi.nlm.nih.gov/pubmed/26989097 Genome-wide association study of response to cognitive-behavioural therapy in children with anxiety disorders. Response to cognitive-behavioural therapy in anxiety disorder Up to 902 European ancestry cases, up to 78 cases NA Illumina [3017604] (imputed) 12 cognitive behavioural therapy http://www.ebi.ac.uk/efo/EFO_0007820 GCST003469 Genome-wide genotyping array 2017-03-30 27694991 Adams HH 2016-10-03 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/27694991 Novel genetic loci underlying human intracranial volume identified through genome-wide association. Intracranial volume 26,577 European ancestry individuals 2,362 European ancestry individuals, 938 African American individuals, 955 Asian ancestry individuals, 1,605 Hispanic individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 0 intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0004886 GCST003834 Genome-wide genotyping array 2018-04-30 27777418 Wong ML 2016-10-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27777418 The PHF21B gene is associated with major depression and modulates the stress response. Major depressive disorder 203 Mexican American cases, 196 Mexican American controls NA Illumina [83898] 17 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005547 Exome genotyping array [Exome array] 2017-03-27 27639821 Scherag A 2016-09-15 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/27639821 Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality. Mortality in sepsis 149 European ancestry cases, 591 European ancestry controls up to 2,534 individuals Illumina [7993459] (imputed) 15 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST003817 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Insulin sensitivity index up to 4,565 European individuals, up to 413 Old Order Amish (founder/genetic isolate) individuals 20,514 non-diabetic individuals Affymetrix, Illumina [at least 1961018] (imputed) 1 insulin sensitivity measurement http://www.ebi.ac.uk/efo/EFO_0004471 GCST005221 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Insulin levels up to 4,483 European individuals, up to 441 Old Order Amish (founder/genetic isolate) individuals 20,792 European individuals Affymetrix, Illumina [at least 1961018] (imputed) 2 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST005220 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Insulin levels adjusted for BMI up to 4,409 European individuals, up to 411 Old Order Amish (founder/genetic isolate) individuals 18,535 European individuals Affymetrix, Illumina [at least 1961018] (imputed) 4 insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008473 GCST005217 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Insulin disposition index up to 4,746 European individuals, up to 412 Old Order Amish (founder/genetic isolate) individuals 20,461 European individuals Affymetrix, Illumina [at least 1961018] (imputed) 4 disposition index measurement http://www.ebi.ac.uk/efo/EFO_0006832 GCST005222 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Ratio of the area under the curve for insulin and the area under the curve for glucose up to 4,231 European individuals, up to 413 Old Order Amish (founder/genetic isolate) individuals 20,513 European individuals Affymetrix, Illumina [at least 1961018] (imputed) 1 insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008473 GCST005223 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Area under the curve of insulin levels up to 4,324 European individuals, up to 413 Old Order Amish (founder/genetic isolate) individuals 20,620 European individuals Affymetrix, Illumina [at least 1961018] (imputed) 2 insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008473 GCST005218 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Incremental insulin up to 4,447 European individuals, up to 411 Old Order Amish (founder/genetic isolate) individuals 20,706 European individuals NR [at least 1961018] (imputed) 3 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST005219 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Corrected insulin response up to 4,961 European individuals, up to 411 Old Order Amish (founder/genetic isolate) individuals 20,722 European individuals Affymetrix, Illumina [at least 1961018] (imputed) 6 insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008473 GCST005215 Genome-wide genotyping array 2018-01-30 24699409 Prokopenko I 2014-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24699409 A central role for GRB10 in regulation of islet function in man. Corrected insulin response adjusted for insulin sensitivity index up to 4,565 European individuals, up to 413 Old Order Amish (founder/genetic isolate) individuals 20,461 European individuals Affymetrix, Illumina [at least 1961018] (imputed) 6 insulin sensitivity measurement, insulin response measurement http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0008473 GCST005216 Genome-wide genotyping array 2016-12-14 27064256 Khor CC 2016-04-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27064256 Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma. Glaucoma (primary angle closure) 5,612 East Asian ancestry cases, 12,451 East Asian ancestry controls, 337 Indian ancestry cases, 2,538 Indian ancestry controls, 576 European ancestry cases, 4,940 European ancestry controls 430 European ancestry cases, 3,133 European ancestry controls, 90 Nepalese ancestry cases, 205 Nepalese ancestry controls, 2,340 East Asian ancestry cases, 3,865 East Asian ancestry controls, 628 South Asian ancestry cases, 552 South Asian ancestry controls, 99 Latin American cases, 224 Latin American controls, 391 Saudi Arabian ancestry cases, 1,659 Saudi Arabian ancestry controls Illumina [5245080] (imputed) 17 primary angle closure glaucoma http://www.ebi.ac.uk/efo/EFO_1001506 GCST003467 Genome-wide genotyping array 2017-03-31 27701424 Castano-Betancourt MC 2016-10-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27701424 Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis. Hip minimal joint space width 6,523 European ancestry individuals, 6,490 individuals 1,572 European ancestry individuals, 6,655 individuals Illumina [2385183] (imputed) 9 cartilage thickness measurement http://www.ebi.ac.uk/efo/EFO_0007873 GCST003853 Genome-wide genotyping array 2017-03-31 27704462 Moura Rodrigues R 2016-10-04 Immunol Res www.ncbi.nlm.nih.gov/pubmed/27704462 Genome-wide scan in two groups of HIV-infected patients treated with dendritic cell-based immunotherapy. Response to dendritic cell-based immunotherapy in HIV infection 7 Spanish good responders, 8 Brazilian good responders, 8 Spanish poor responders, 10 Brazilian poor responders. NA Illumina [39108] 0 response to dendritic cell-based immunotherapy http://www.ebi.ac.uk/efo/EFO_0007880 GCST003852 Genome-wide genotyping array 2017-11-17 28990359 Polimanti R 2017-10-09 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28990359 Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors. Risky sexual behaviors (alcohol dependence interaction) 454 African American women cases, 1,087 African American men cases, 444 European ancestry women cases, 992 European ancestry men cases, 231 African American women controls, 401 African American men controls, 142 European ancestry women controls, 173 European ancestry men controls Illumina [at least 550000] (imputed) 7 alcohol dependence, risky sexual behaviour measurement http://purl.obolibrary.org/obo/MONDO_0007079, http://www.ebi.ac.uk/efo/EFO_0007877 GCST004956 Genome-wide genotyping array 2017-11-17 28990359 Polimanti R 2017-10-09 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28990359 Ancestry-specific and sex-specific risk alleles identified in a genome-wide gene-by-alcohol dependence interaction study of risky sexual behaviors. Risky sexual behaviors in alcohol dependence 454 African American women individuals, 1,087 African American men individuals, 444 European ancestry women individuals, 992 European ancestry men individuals. NA Illumina [at least 550000] (imputed) 4 risky sexual behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007877 GCST004955 Genome-wide genotyping array 2018-03-16 29408531 Zhang D 2018-02-02 Gene www.ncbi.nlm.nih.gov/pubmed/29408531 The polymorphism rs671 at ALDH2 associated with serum uric acid levels in Chinese Han males: A genome-wide association study. Serum uric acid levels 1,634 Han Chinese ancestry individuals 2,818 Han Chinese ancestry individuals Illumina [532842] 2 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST005369 Genome-wide genotyping array 2018-02-02 29217827 Sanders AR 2017-12-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29217827 Genome-Wide Association Study of Male Sexual Orientation. Male sexual orientation 1,077 European ancestry homosexual men, 1,231 European ancestry heterosexual men NA Affymetrix [5642880] (imputed) 2 male homosexuality http://www.ebi.ac.uk/efo/EFO_0008486 GCST005247 Genome-wide genotyping array 2018-03-12 29346644 Yan Q 2018-01-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29346644 Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration. Disease progression in age-related macular degeneration 1,105 progressed eyes and 3,912 non-progressed eyes from 2,721 European ancestry individuals NA Illumina [8974355] (imputed) 28 age-related macular degeneration, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0001365, http://www.ebi.ac.uk/efo/EFO_0008336 GCST005359 Genome-wide genotyping array 2018-03-12 29346644 Yan Q 2018-01-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29346644 Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration. Disease progression to geographic atrophy form in age-related macular degeneration 615 progressed eyes and 3,912 non-progressed eyes from up to 2,721 European ancestry individuals NA Illumina [8974355] (imputed) 2 atrophic macular degeneration, disease progression measurement http://www.ebi.ac.uk/efo/EFO_1001492, http://www.ebi.ac.uk/efo/EFO_0008336 GCST005360 Genome-wide genotyping array 2018-03-12 29346644 Yan Q 2018-01-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29346644 Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration. Disease progression to choroidal neovascularization form in age-related macular degeneration 508 progressed eyes and 3,912 non-progressed eyes from up to 2,721 European ancestry individuals NA Illumina [8974355] (imputed) 4 disease progression measurement, wet macular degeneration http://www.ebi.ac.uk/efo/EFO_0008336, http://www.ebi.ac.uk/efo/EFO_0004683 GCST005358 Genome-wide genotyping array 2019-12-02 29346644 Yan Q 2018-01-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29346644 Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration. Disease progression in age-related macular degeneration (adjusted for baseline) 1,105 progressed eyes and 3,912 non-progressed eyes from 2,721 European ancestry individuals NA Illumina [8974355] (imputed) 34 disease progression measurement http://www.ebi.ac.uk/efo/EFO_0008336 GCST009144 Genome-wide genotyping array 2017-07-27 25521368 Tonjes A 2014-12-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25521368 Genome wide meta-analysis highlights the role of genetic variation in RARRES2 in the regulation of circulating serum chemerin. Circulating chemerin levels 1,967 European ancestry individuals, 824 Sorbian (founder/genetic isolate) individuals 967 individuals Affymetrix [2023499] (imputed) 6 chemerin measurement http://www.ebi.ac.uk/efo/EFO_0004573 GCST004389 Genome-wide genotyping array 2018-02-05 29330379 Zuber V 2018-01-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29330379 Identification of shared genetic variants between schizophrenia and lung cancer. Schizophrenia or lung cancer (pleiotropy) 32,405 European and unknown ancestry schizophrenia cases, 12,160 European and unknown ancestry lung cancer cases, 59,059 European and unknown ancestry controls NA NR [up to 2558411] 0 lung carcinoma, schizophrenia http://www.ebi.ac.uk/efo/EFO_0001071, http://purl.obolibrary.org/obo/MONDO_0005090 GCST005267 Genome-wide genotyping array 2018-02-05 29330379 Zuber V 2018-01-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29330379 Identification of shared genetic variants between schizophrenia and lung cancer. Schizophrenia or cigarettes per day (pleiotropy) 32,405 European and unknown ancestry schizophrenia cases, 74,503 smoker individuals, 42,221 European and unknown ancestry controls NA NR [up to 2558411] 0 schizophrenia, cigarettes per day measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0006525 GCST005266 Genome-wide genotyping array 2017-09-14 24166409 Gelernter J 2014-01-01 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24166409 Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. Alcohol dependence 4,629 African American individuals, 5,131 European ancestry individuals 801 African American individuals, 1,746 European ancestry individuals Illumina [up to 10421983] (imputed) 49 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST004711 Genome-wide genotyping array 2017-09-14 24166409 Gelernter J 2014-01-01 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24166409 Genome-wide association study of alcohol dependence:significant findings in African- and European-Americans including novel risk loci. Alcohol dependence 2,415 African American cases, 1,798 African American controls, 2,669 European ancestry cases, 2,002 European ancestry controls 324 African American cases, 327 African American controls, 2,269 European ancestry cases, 2,975 European ancestry controls Illumina [up to 10421983] (imputed) 19 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST004712 Genome-wide genotyping array 2017-08-10 27325353 Matteini AM 2016-06-21 Aging Cell www.ncbi.nlm.nih.gov/pubmed/27325353 GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium. Hand grip strength 27,581 European ancestry individuals 6,393 individuals Affymetrix, Illumina [2725778] (imputed) 4 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST004494 Genome-wide genotyping array 2017-08-10 27325353 Matteini AM 2016-06-21 Aging Cell www.ncbi.nlm.nih.gov/pubmed/27325353 GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium. Lower body strength 9,822 European ancestry individuals NA Affymetrix, Illumina [2725778] (imputed) 11 lower body strength measurement http://www.ebi.ac.uk/efo/EFO_0007999 GCST004493 Genome-wide genotyping array 2018-02-23 29326435 Hill WD 2018-01-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29326435 A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. Intelligence (MTAG) 120,934 British ancestry individuals, 127,548 individuals NA Affymetrix [NR] 645 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST005316 Genome-wide genotyping array 2017-09-28 28703219 Son HY 2017-07-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28703219 Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer. Differentiated thyroid cancer 470 Korean ancestry cases, 8,279 Korean ancestry controls 615 Korean ancestry cases, 605 Korean ancestry controls Affymetrix, Illumina [3593389] (imputed) 10 differentiated thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_1002017 GCST004798 Genome-wide genotyping array 2017-09-19 28703219 Son HY 2017-07-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28703219 Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer. Papillary thyroid cancer 410 Korean ancestry cases, 8,279 Korean ancestry controls 587 Korean ancestry cases, 605 Korean ancestry controls Affymetrix, Illumina [3593389] (imputed) 9 papillary thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0000641 GCST004753 Genome-wide genotyping array 2017-09-19 28703219 Son HY 2017-07-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28703219 Genome-wide association and expression quantitative trait loci studies identify multiple susceptibility loci for thyroid cancer. Follicular thyroid cancer 60 Korean ancestry cases, 8,279 Korean ancestry controls 28 Korean ancestry cases, 605 Korean ancestry controls Affymetrix, Illumina [3593389] (imputed) 0 follicular thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0000501 GCST004754 Genome-wide genotyping array 2017-08-08 27363682 Mitchell JS 2016-07-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27363682 Genome-wide association study identifies multiple susceptibility loci for multiple myeloma. Multiple myeloma 7,319 European ancestry cases, 234,385 European ancestry controls 2,547 European ancestry cases, 4,803 European ancestry controls Illumina [at least 7182761] (imputed) 23 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST004483 Genome-wide genotyping array 2017-09-28 28763065 Xia K 2017-08-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/28763065 Genome-wide association analysis identifies common variants influencing infant brain volumes. Brain volume in infants (white matter) 295 European, African American, Asian, Native American and other admixed ancestry infants, 17 European, African American, Asian, Native American and other admixed ancestry sibling pairs, 116 European, African American, Asian, Native American and other admixed ancestry twin pairs. NA Affymetrix [8762422] (imputed) 6 infant white matter volume measurement http://www.ebi.ac.uk/efo/EFO_0008370 GCST004795 Genome-wide genotyping array 2017-09-28 28763065 Xia K 2017-08-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/28763065 Genome-wide association analysis identifies common variants influencing infant brain volumes. Brain volume in infants (cerebrospinal fluid) 295 European, African American, Asian, Native American and other admixed ancestry infants, 17 European, African American, Asian, Native American and other admixed ancestry sibling pairs, 116 European, African American, Asian, Native American and other admixed ancestry twin pairs. NA Affymetrix [8762422] (imputed) 4 infant cerebrospinal fluid volume measurement http://www.ebi.ac.uk/efo/EFO_0008367 GCST004796 Genome-wide genotyping array 2017-09-28 28763065 Xia K 2017-08-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/28763065 Genome-wide association analysis identifies common variants influencing infant brain volumes. Brain volume in infants (grey matter) 295 European, African American, Asian, Native American and other admixed ancestry infants, 17 European, African American, Asian, Native American and other admixed ancestry sibling pairs, 116 European, African American, Asian, Native American and other admixed ancestry twin pairs. NA Affymetrix [8762422] (imputed) 12 infant grey matter volume measurement http://www.ebi.ac.uk/efo/EFO_0008368 GCST004797 Genome-wide genotyping array 2017-09-28 28763065 Xia K 2017-08-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/28763065 Genome-wide association analysis identifies common variants influencing infant brain volumes. Brain volume in infants (intracranial brain volume) 295 European, African American, Asian, Native American and other admixed ancestry infants, 17 European, African American, Asian, Native American and other admixed ancestry sibling pairs, 116 European, African American, Asian, Native American and other admixed ancestry twin pairs. NA Affymetrix [8762422] (imputed) 3 infant intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0008369 GCST004794 Genome-wide genotyping array 2017-09-28 28738859 de Jong K 2017-07-24 Respir Res www.ncbi.nlm.nih.gov/pubmed/28738859 Genes and pathways underlying susceptibility to impaired lung function in the context of environmental tobacco smoke exposure. Forced expiratory volume in 1 second (environmental tobacco smoke interaction) 10,817 European ancestry individuals 1,156 European ancestry individuals, 1,276 individuals Illumina [227981] 3 forced expiratory volume, environmental tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0008361 GCST004800 Genome-wide genotyping array 2017-03-14 27623284 Verma SS 2016-09-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27623284 Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium. Glaucoma (primary open-angle) 14 Black cases, 922 European ancestry cases, 25 cases, 82 Black controls, 3,918 European ancestry controls, 129 controls NA NR [2914185] 2 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST003745 Genome-wide genotyping array 2017-03-21 28173075 Niu N 2016-09-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28173075 Metformin pharmacogenomics: a genome-wide association study to identify genetic and epigenetic biomarkers involved in metformin anticancer response using human lymphoblastoid cell lines. Response to metformin (IC50) up to 96 African American lymphoblastoid cell lines, up to 96 Han Chinese American lymphoblastoid cell lines, up to 96 European ancestry lymphoblastoid cell lines NA Affymetrix, Illumina [~ 6700000] (imputed) 12 cytotoxicity measurement, response to metformin http://www.ebi.ac.uk/efo/EFO_0006952, http://purl.obolibrary.org/obo/GO_1901558 GCST003791 Genome-wide genotyping array 2017-01-27 27195708 Scott WR 2016-05-19 PLoS One www.ncbi.nlm.nih.gov/pubmed/27195708 Investigation of Genetic Variation Underlying Central Obesity amongst South Asians. Waist-to-hip ratio adjusted for body mass index 10,318 South Asian ancestry individuals 1,922 South Asian ancestry individuals Affymetrix, Illumina, Perlegen [6571328] (imputed) 7 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST003564 Genome-wide genotyping array 2017-03-24 27758888 Ingle JN 2016-10-10 Cancer Res www.ncbi.nlm.nih.gov/pubmed/27758888 Genetic Polymorphisms in the Long Noncoding RNA MIR2052HG Offer a Pharmacogenomic Basis for the Response of Breast Cancer Patients to Aromatase Inhibitor Therapy. Breast cancer-free interval (treatment with aromatase inhibitor) 6 African American recurrent cases, 134 African American controls without recurrence, 243 European ancestry recurrent cases, 4,216 European ancestry controls without recurrence, 3 Asian ancestry recurrent cases, 56 Asian ancestry controls without recurrence NA Illumina [~ 7400000] (imputed) 1 disease free survival, response to aromatase inhibitor http://www.ebi.ac.uk/efo/EFO_0000409, http://purl.obolibrary.org/obo/GO_0061477 GCST003816 Genome-wide genotyping array 2017-01-16 27151647 Chen G 2016-05-05 Addict Biol www.ncbi.nlm.nih.gov/pubmed/27151647 An association study revealed substantial effects of dominance, epistasis and substance dependence co-morbidity on alcohol dependence symptom count. Alcohol dependence symptom count 2,605 European ancestry individuals, 1,233 African American individuals NA Illumina [974863] 6 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST003538 Genome-wide genotyping array 2017-03-24 27770636 Mez J 2016-10-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/27770636 Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans. Late-onset Alzheimer's disease 1,825 African American ancestry cases, 3,784 African American ancestry controls NR [19725427] (imputed) 123 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST003815 Genome-wide genotyping array 2017-03-17 27702942 Tang CS 2016-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27702942 Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. Hirschsprung disease 212 European ancestry cases, 173 Chinese ancestry cases, 122 Korean ancestry cases, 202 European ancestry controls, 615 Chinese ancestry controls, 374 Korean ancestry controls NA Affymetrix, Illumina [at least 6512116] (imputed) 7 Hirschsprung disease http://purl.obolibrary.org/obo/MONDO_0018309 GCST003764 Genome-wide genotyping array 2017-03-24 27694927 Vijayakrishnan J 2016-10-03 Leukemia www.ncbi.nlm.nih.gov/pubmed/27694927 A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1. Acute lymphoblastic leukemia in childhood (B cell precursor) 1,658 European ancestry child cases, 7,224 European ancestry controls 1,109 child cases, 1,412 European ancestry child cases, 2,085 controls, 1,479 European ancestry controls Illumina [11700000] (imputed) 2 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST003798 Genome-wide genotyping array 2018-01-29 29220522 Liu F 2017-12-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29220522 Meta-analysis of genome-wide association studies identifies 8 novel loci involved in shape variation of human head hair. Hair shape 16,763 European ancestry individuals 2,340 European ancestry individuals, 2,899 Han Chinese ancestry individuals, 709 Uyghur ancestry individuals, 6,238 Latin American individuals, 15 South American, South Asian or Middle Eastern individuals Illumina [up to 9350000] (imputed) 11 hair shape measurement http://www.ebi.ac.uk/efo/EFO_0007824 GCST005191 Genome-wide genotyping array 2016-12-06 27064253 Zhou W 2016-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27064253 Mosaic loss of chromosome Y is associated with common variation near TCL1A. Mosaic loss of chromosome Y 895 cases, 11,474 controls NA Illumina [2595310] 1 mosaic loss of chromosome Y measurement http://www.ebi.ac.uk/efo/EFO_0007783 GCST003421 Genome-wide genotyping array 2018-01-29 29212778 van der Harst P 2017-12-06 Circ Res www.ncbi.nlm.nih.gov/pubmed/29212778 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. Coronary artery disease 34,541 cases, 261,984 controls 88,192 cases, 162,544 controls Affymetrix [7947838] (imputed) 259 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST005194 Genome-wide genotyping array 2018-01-29 29212778 van der Harst P 2017-12-06 Circ Res www.ncbi.nlm.nih.gov/pubmed/29212778 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. Coronary artery disease up to 122,733 cases, up to 424,528 controls NA Affymetrix [at least 7947838] (imputed) 148 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST005195 Genome-wide genotyping array 2018-01-29 29212778 van der Harst P 2017-12-06 Circ Res www.ncbi.nlm.nih.gov/pubmed/29212778 Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease. Coronary artery disease 88,192 cases, 162,544 controls 34,541 cases, 261,984 controls NR [8041861] (imputed) 254 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST005196 Genome-wide genotyping array 2017-12-20 29121268 Amare AT 2017-11-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/29121268 Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study. Bipolar disorder lithium response (continuous) or schizophrenia 2,366 European ancestry lithium treated bipolar disorder cases, 220 Asian ancestry lithium treated bipolar disorder cases, 36,989 schizophrenia cases, controls (see Ripke et al 2014 PMID:25056061) NA NR [NR] (imputed) 8 bipolar disorder, schizophrenia, response to lithium ion http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/GO_0010226 GCST005081 Genome-wide genotyping array 2017-12-20 29121268 Amare AT 2017-11-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/29121268 Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study. Bipolar disorder lithium response (categorical) or schizophrenia 704 European and East Asian ancestry lithium responder bipolar disorder cases, 1,662 European and East Asian ancestry lithium non-responder bipolar disorder controls, 36,989 schizophrenia cases, controls (see Ripke 2014 PMID:25056061). NA NR [NR] (imputed) 8 bipolar disorder, schizophrenia, response to lithium ion http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/GO_0010226 GCST005082 Genome-wide genotyping array 2018-01-17 29210060 Koster R 2017-12-06 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/29210060 Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients. Overall survival in osteosarcoma 523 European ancestry individuals 109 Brazilian ancestry individuals Illumina [510856] 9 osteosarcoma, overall survival http://www.ebi.ac.uk/efo/EFO_0000637, http://www.ebi.ac.uk/efo/EFO_0000638 GCST005158 Genome-wide genotyping array 2019-08-21 25854761 Zuo X 2015-04-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25854761 Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis. Psoriasis 11,245 Han Chinese ancestry cases, 11,177 Han Chinese ancestry controls 6,369 Han Chinese ancestry cases, 13,969 Han Chinese ancestry controls Illumina [87827] 34 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST008479 Exome genotyping array [Exome array] 2018-01-10 29145611 Hu Y 2017-11-14 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/29145611 Identification of Novel Potentially Pleiotropic Variants Associated With Osteoporosis and Obesity Using the cFDR Method. Osteoporosis or obesity (pleiotropy) 53,236 European ancestry individuals (femoral neck BMI), 322,154 European ancestry individuals (BMI), 17,070 individuals (BMI), 210,088 European ancestry individuals (WHR), 14,371 individuals (WHR) NA NR [> 2000000] 0 obesity, osteoporosis http://www.ebi.ac.uk/efo/EFO_0001073, http://www.ebi.ac.uk/efo/EFO_0003882 GCST005114 Genome-wide genotyping array 2019-01-11 26401656 Burkhardt R 2015-09-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26401656 Integration of Genome-Wide SNP Data and Gene-Expression Profiles Reveals Six Novel Loci and Regulatory Mechanisms for Amino Acids and Acylcarnitines in Whole Blood. Blood metabolite levels 2,107 European ancestry individuals 923 Sorbian (founder/genetic isolate) individuals Affymetrix [2619023] (imputed) 25 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST006879 Genome-wide genotyping array 2017-12-19 27029810 Joshi PK 2016-03-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27029810 Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan. Mortality 138,536 British ancestry mothers, 133,545 British ancestry fathers 24,168 European ancestry individuals, 681 African ancestry individuals, 962 Afro-Caribbean individuals, 1,613 South Asian ancestry individuals, 338 Chinese ancestry individuals Affymetrix [73355667] (imputed) 2 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST005078 Genome-wide genotyping array 2017-12-20 29147026 Chen CH 2017-11-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29147026 Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure. Putamen volume 12,596 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 10 putamen volume http://www.ebi.ac.uk/efo/EFO_0006932 GCST005083 Genome-wide genotyping array 2017-01-27 27191271 Hu Q 2016-05-13 Oncotarget www.ncbi.nlm.nih.gov/pubmed/27191271 NPR-C gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a multicenter study. Coronary artery disease 393 Han Chinese ancestry cases, 393 Han Chinese ancestry controls 4,537 Han Chinese ancestry cases, 4,590 Han Chinese ancestry controls Illumina [872261] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST003561 Genome-wide genotyping array 2017-12-01 29065906 Joo YB 2017-10-25 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/29065906 Biological function integrated prediction of severe radiographic progression in rheumatoid arthritis: a nested case control study. Severe progression in rheumatoid arthritis 120 Korean ancestry cases, 118 Korean ancestry controls NA Illumina [1343748] 2 rheumatoid arthritis, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0008336 GCST004998 Genome-wide genotyping array 2017-12-20 29170203 Alonso N 2017-11-23 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29170203 Identification of a novel locus on chromosome 2q13, which predisposes to clinical vertebral fractures independently of bone density. Fractures (vertebral) 1,553 European ancestry cases, 4,340 European ancestry controls 694 European ancestry cases, 2,105 European ancestry controls, 334 cases, 1,657 controls Affymetrix, Illumina [2366456] (imputed) 3 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST005097 Genome-wide genotyping array 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Autoimmune hepatitis in primary sclerosing cholangitis 107 European ancestry cases, 3,159 European ancestry controls NA Illumina [130422] (imputed) 3 Autoimmune Hepatitis http://www.ebi.ac.uk/efo/EFO_0005676 GCST005853 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Primary sclerosing cholangitis (small duct vs large duct) 75 European ancestry small duct cases, 3,159 European ancestry large duct cases NA Illumina [130422] 0 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST005854 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Liver transplant-free survival in primary sclerosing cholangitis (time to event) 874 European ancestry liver transplantation cases , 2,444 European ancestry liver transplant-free cases NA Illumina [130422] 3 event free survival time, sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0000482, http://www.ebi.ac.uk/efo/EFO_0004268 GCST005859 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Colectomy in primary sclerosing cholangitis 419 European ancestry colectomy cases, 2,897 European non-colectomy controls NA Illumina [130422] 0 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST005852 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Cholangiocarcinoma in primary sclerosing cholangitis 188 European ancestry cases, 3,147 European ancestry controls NA Illumina [130422] 1 cholangiocarcinoma http://www.ebi.ac.uk/efo/EFO_0005221 GCST005855 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Cholangiocarcinoma in primary sclerosing cholangitis (time to event) 188 European ancestry cholangiocarcinoma cases, 3,147 European ancestry cholangiocarcinoma-free cases NA Illumina [130422] 3 event free survival time, cholangiocarcinoma, sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0000482, http://www.ebi.ac.uk/efo/EFO_0005221, http://www.ebi.ac.uk/efo/EFO_0004268 GCST005860 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Colorectal carcinoma in primary sclerosing cholangitis 127 European ancestry cases, 2,822 European ancestry controls NA Illumina [130422] 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST005856 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Gallbladder carcinoma in primary sclerosing cholangitis 30 European ancestry cases, 2,977 European ancestry controls NA Illumina [130422] 0 gallbladder neoplasm http://www.ebi.ac.uk/efo/EFO_0004606 GCST005857 Targeted genotyping array [ImmunoChip] 2018-07-12 28779025 Alberts R 2017-08-04 Gut www.ncbi.nlm.nih.gov/pubmed/28779025 Genetic association analysis identifies variants associated with disease progression in primary sclerosing cholangitis. Hepatocellular carcinoma in primary sclerosing cholangitis 22 European ancestry cases, 2,984 European ancestry controls NA Illumina [130422] 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST005858 Targeted genotyping array [ImmunoChip] 2017-02-18 27193031 Marquez A 2016-05-18 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/27193031 A combined large-scale meta-analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus. Systemic lupus erythematosus or rheumatoid arthritis 2,237 European ancestry systemic lupus erythematosus cases, 3,911 European ancestry rheumatoid arthritis cases, 10,398 European ancestry controls 1,957 European ancestry systemic lupus erythematosus cases, 13,641 European ancestry rheumatoid arthritis cases, 36,509 European ancestry controls NR [at least 309839] (imputed) 9 rheumatoid arthritis, systemic lupus erythematosus http://www.ebi.ac.uk/efo/EFO_0000685, http://purl.obolibrary.org/obo/MONDO_0007915 GCST003620 Genome-wide genotyping array 2016-07-15 27186693 Aydin-Son Y 2015-07-01 Turk J Pediatr www.ncbi.nlm.nih.gov/pubmed/27186693 Systems-level analysis of genome wide association study results for a pilot juvenile idiopathic arthritis family study. Arthritis (juvenile idiopathic) 13 Caucasian Eastern Mediterranean ancestry oligoarticular case-parent trios, 13 Caucasian Eastern Mediterranean ancestry rheumatoid factor negative polyarticular case-parent trios NA Affymetrix [249676] 0 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST003011 Genome-wide genotyping array 2019-09-10 26498133 Arya R 2015-08-26 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/26498133 Genetic Variants Influencing Joint Damage in Mexican Americans and European Americans With Rheumatoid Arthritis. Joint damage in rheumatoid arthritis 666 Mexican ancestry cases, 407 European ancestry cases NA Illumina [at least 127563] (imputed) 2 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST008643 Targeted genotyping array [ImmunoChip] 2017-02-16 27203581 Sousa I 2016-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/27203581 Multicentric Genome-Wide Association Study for Primary Spontaneous Pneumothorax. Primary spontaneous pneumothorax 92 Portuguese ancestry cases, 129 Portuguese ancestry controls 100 Portuguese ancestry cases, 425 Portuguese ancestry controls Affymetrix [868260] 0 Spontaneous pneumothorax http://purl.obolibrary.org/obo/HP_0002108 GCST003618 Genome-wide genotyping array 2017-05-24 28059113 Hao J 2017-01-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28059113 Genome-wide association study identifies COL2A1 locus involved in the hand development failure of Kashin-Beck disease. Palmar length-width ratio in Kashin-Beck disease 90 Han Chinese ancestry individuals 403 Han Chinese ancestry individuals Affymetrix [532894] 0 Kashin-Beck disease http://www.ebi.ac.uk/efo/EFO_0006511 GCST004091 Genome-wide genotyping array 2018-08-14 29899525 Klimentidis YC 2018-06-13 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/29899525 Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. Accelerometer-based physical activity measurement (fraction of time with accelerations >425 milli-gravities) 90,667 European ancestry individuals NA Affymetrix [11800000] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006079 Genome-wide genotyping array 2018-08-16 29899525 Klimentidis YC 2018-06-13 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/29899525 Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. Moderate to vigorous physical activity levels 377,234 European ancestry individuals NA Affymetrix [11800000] (imputed) 13 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006097 Genome-wide genotyping array 2018-08-16 29899525 Klimentidis YC 2018-06-13 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/29899525 Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. Vigorous physical activity 98,060 European ancestry active cases, 162,995 European ancestry inactive controls NA Affymetrix [11800000] (imputed) 9 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006098 Genome-wide genotyping array 2018-08-16 29899525 Klimentidis YC 2018-06-13 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/29899525 Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. Strenuous sports or other exercises 124,842 European ancestry active cases, 225,650 European ancestry inactive controls NA Affymetrix [11800000] (imputed) 8 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006100 Genome-wide genotyping array 2018-08-16 29899525 Klimentidis YC 2018-06-13 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/29899525 Genome-wide association study of habitual physical activity in over 377,000 UK Biobank participants identifies multiple variants including CADM2 and APOE. Accelerometer-based physical activity measurement (average acceleration) 91,084 European ancestry individuals NA Affymetrix [11800000] (imputed) 5 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006099 Genome-wide genotyping array 2019-08-14 25771307 Watson AL 2015-02-26 Diabetes Res Clin Pract www.ncbi.nlm.nih.gov/pubmed/25771307 Single nucleotide polymorphisms in type 2 diabetes among Hispanic adults. Type 2 diabetes 18 Hispanic cases, 18 Hispanic controls NA Illumina [132623] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST008434 Targeted genotyping array [Cardio-MetaboChip] 2017-11-14 25751625 Michailidou K 2015-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25751625 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Breast cancer 15,748 European ancestry cases, 18,084 European ancestry controls 46,785 European ancestry cases, 42,892 European ancestry controls Affymetrix, Illumina [~ 11600000] (imputed) 88 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST004950 Genome-wide genotyping array 2019-02-28 25751625 Michailidou K 2015-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25751625 Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer. Breast cancer 46,785 European ancestry cases, 42,892 European ancestry controls NA Affymetrix, Illumina [~ 14000000] (imputed) 74 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST007236 Genome-wide genotyping array 2016-12-21 27167565 Stein MB 2016-05-11 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/27167565 Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers. Post-traumatic stress disorder 2140 European ancestry cases, 497 African American ancestry cases, 530 Latino American ancestry cases, 2909 European ancestry trauma-exposed controls, 815 African American ancestry trauma-exposed controls, 883 Latino American ancestry trauma-exposed controls. 672 European ancestry cases, 97 African American ancestry cases, 178 Latino American ancestry cases, 3335 European ancestry trauma-exposed controls, 570 African American ancestry trauma-exposed controls, 1064 Latino American ancestry trauma-exposed controls. Illumina [664457] (imputed) 1 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST003495 Genome-wide genotyping array 2017-11-06 28957430 Winsvold BS 2017-09-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28957430 Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants. Migraine or coronary artery disease 37,653 coronary artery disease cases, 22,120 migraine cases, 171,108 controls NA Affymetrix, Illumina [NR] 0 migraine disorder, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0001645 GCST004944 Genome-wide genotyping array 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery external diameter 3,681 individuals NA Illumina [101597] 1 carotid artery external diameter measurement http://www.ebi.ac.uk/efo/EFO_0007719 GCST008979 Exome genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery internal diameter 3,681 individuals NA Illumina [101597] 1 carotid artery internal diameter measurement http://www.ebi.ac.uk/efo/EFO_0007720 GCST008982 Targeted genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. LDL cholesterol 3,681 individuals NA Illumina [101597] 5 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008988 Exome genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Triglycerides 3,681 individuals NA Illumina [101597] 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008985 Targeted genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery stiffness 3,681 individuals NA Illumina [101597] 0 carotid artery stiffness measurement http://www.ebi.ac.uk/efo/EFO_0007718 GCST008981 Targeted genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery intima media thickness 3,681 individuals NA Illumina [101597] 0 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST008989 Exome genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery mean blood pressure 3,681 individuals NA Illumina [101597] 0 carotid artery mean blood pressure measurement http://www.ebi.ac.uk/efo/EFO_0007723 GCST008986 Exome genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. HDL cholesterol 3,681 individuals NA Illumina [101597] 6 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008987 Exome genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery central pulse pressure 3,681 individuals NA Illumina [101597] 0 carotid artery central pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0007721 GCST008980 Targeted genotyping array [Illumina HumanExome-12v1.1 BeadChip] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery circumferential wall stress 3,681 individuals NA Illumina [101597] 0 carotid artery circumferential wall stress measurement http://www.ebi.ac.uk/efo/EFO_0007724 GCST008983 Targeted genotyping array [Exome array] 2019-10-30 26160806 Proust C 2015-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26160806 Contribution of Rare and Common Genetic Variants to Plasma Lipid Levels and Carotid Stiffness and Geometry: A Substudy of the Paris Prospective Study 3. Carotid artery wall cross sectional area 3,681 individuals NA Illumina [101597] 0 carotid artery wall cross sectional area measurement http://www.ebi.ac.uk/efo/EFO_0007722 GCST008984 Targeted genotyping array [Exome array] 2017-06-01 28053049 Sennblad B 2017-02-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28053049 Genome-wide association study with additional genetic and post-transcriptional analyses reveals novel regulators of plasma factor XI levels. Factor XI 16,169 European ancestry individuals 2,045 European ancestry individuals Affymetrix, Illumina [7353638] (imputed) 2 factor XI measurement http://www.ebi.ac.uk/efo/EFO_0004694 GCST004124 Genome-wide genotyping array 2017-02-19 27195777 Sano M 2016-05-19 PLoS One www.ncbi.nlm.nih.gov/pubmed/27195777 Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population. Left ventricular QRS voltage 2,994 Japanese ancestry individuals 2,941 Japanese ancestry individuals Illumina [~ 2500000] 2 QRS amplitude, S wave amplitude, R wave amplitude http://www.ebi.ac.uk/efo/EFO_0007742, http://www.ebi.ac.uk/efo/EFO_0007740, http://www.ebi.ac.uk/efo/EFO_0007741 GCST003630 Genome-wide genotyping array 2019-09-20 26278503 Huang C 2015-11-01 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/26278503 Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans. Inflammatory bowel disease 1,511 African American cases, 1,797 African American controls NA Illumina [130241] 3 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST008731 Targeted genotyping array [Immunochip] 2019-09-20 26278503 Huang C 2015-11-01 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/26278503 Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans. Crohn's disease 1,088 African American cases, 1,797 African American controls NA Illumina [130241] 1 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST008730 Targeted genotyping array [ImmunoChip] 2019-09-20 26278503 Huang C 2015-11-01 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/26278503 Characterization of genetic loci that affect susceptibility to inflammatory bowel diseases in African Americans. Ulcerative colitis 361 African American cases, 1,797 African American controls NA Illumina [130241] 2 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST008732 Targeted genotyping array [Immunochip] 2017-02-15 27244555 Li Y 2016-05-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27244555 Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese. Persistent hepatitis B virus infection 1,251 Chinese ancestry persistently infected cases, 1,057 Chinese ancestry spontaneously recovered controls 3,905 Chinese ancestry persistently infected cases, 3,356 Chinese ancestry spontaneously recovered controls Affymetrix, Illumina [up to 4494311] (imputed) 4 hepatitis B virus infection, Susceptibility to viral and mycobacterial infections http://www.ebi.ac.uk/efo/EFO_0004197, http://www.orpha.net/ORDO/Orphanet_391311 GCST003615 Genome-wide genotyping array 2017-11-29 29064910 Kure Fischer E 2017-10-23 Int Clin Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/29064910 A molecular pathway analysis informs the genetic risk for arrhythmias during antipsychotic treatment. Antipsychotic drug-induced QTc interval change in schizophrenia 434 European ancestry individuals, 202 African ancestry individuals, 25 individuals NA Affymetrix, Perlegen [1785543] (imputed) 34 heart rate variability measurement, response to antipsychotic drug http://www.ebi.ac.uk/efo/EFO_0008003, http://purl.obolibrary.org/obo/GO_0097332 GCST004987 Genome-wide genotyping array 2017-02-20 27244217 Fogh I 2016-05-31 JAMA Neurol www.ncbi.nlm.nih.gov/pubmed/27244217 Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. Survival in sporadic amyotrophic lateral sclerosis 4,256 European ancestry cases NA Illumina [7174392] (imputed) 6 sporadic amyotrophic lateral sclerosis, survival time http://www.ebi.ac.uk/efo/EFO_0001357, http://www.ebi.ac.uk/efo/EFO_0000714 GCST003632 Genome-wide genotyping array 2018-05-02 29511194 Helgadottir A 2018-03-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29511194 Genome-wide analysis yields new loci associating with aortic valve stenosis. Aortic valve stenosis 2,457 Icelandic ancestry cases, 349,342 Icelandic ancestry controls (including non-array genotyped, whole genome imputed individuals) 4,850 European ancestry cases, 451,731 European ancestry controls Illumina [32500000] (imputed) 5 aortic stenosis http://www.ebi.ac.uk/efo/EFO_0000266 GCST005561 Genome-wide genotyping array, Genome-wide sequencing 2018-07-02 29511167 Theriault S 2018-03-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29511167 A transcriptome-wide association study identifies PALMD as a susceptibility gene for calcific aortic valve stenosis. Calcific aortic valve stenosis 1,009 French Canadian cases, 1,017 French Canadian controls 1,391 European ancestry cases, 352,195 European ancestry controls Illumina [7732680] (imputed) 1 aortic stenosis, aortic valve calcification http://www.ebi.ac.uk/efo/EFO_0000266, http://www.ebi.ac.uk/efo/EFO_0005239 GCST005785 Genome-wide genotyping array 2018-08-21 29518117 Lee HS 2018-03-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/29518117 Nuclear receptor and VEGF pathways for gene-blood lead interactions, on bone mineral density, in Korean smokers. Bone mineral density x blood lead interaction in current smokers (2df test) 119 Korean ancestry current smokers NA Affymetrix [344396] 3 blood lead measurement, bone density http://www.ebi.ac.uk/efo/EFO_0007040, http://www.ebi.ac.uk/efo/EFO_0003923 GCST006133 Genome-wide genotyping array 2018-08-21 29518117 Lee HS 2018-03-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/29518117 Nuclear receptor and VEGF pathways for gene-blood lead interactions, on bone mineral density, in Korean smokers. Bone mineral density x blood lead interaction in current smokers (1df test) 119 Korean ancestry current smokers NA Affymetrix [344396] 1 blood lead measurement, bone density http://www.ebi.ac.uk/efo/EFO_0007040, http://www.ebi.ac.uk/efo/EFO_0003923 GCST006132 Genome-wide genotyping array 2017-12-05 29065852 Hallengren E 2017-10-24 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/29065852 Genetic determinants of growth hormone and GH-related phenotypes. Fasting growth hormone levels 4,134 Swedish ancestry individuals 5,262 Swedish ancestry individuals Illumina [659208] 0 growth hormone measurement http://www.ebi.ac.uk/efo/EFO_0008438 GCST005035 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced severe leukopenia in inflammatory bowel disease (conditioned on rs116855232) 72 Japanese ancestry cases, 1,148 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 0 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006200 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced leukopenia in inflammatory bowel disease 196 Japanese ancestry cases, 1,024 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 2 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006201 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced leukopenia in inflammatory bowel disease (conditioned on rs116855232) 196 Japanese ancestry cases, 1,024 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 1 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006202 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced severe leukopenia in inflammatory bowel disease 72 Japanese ancestry cases, 1,148 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 1 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006204 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced acute severe leukopenia in inflammatory bowel disease 43 Japanese ancestry cases, 1,172 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 1 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006205 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced alopecia in inflammatory bowel disease 81 Japanese ancestry cases, 1,139 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 5 alopecia, response to thiopurine http://purl.obolibrary.org/obo/MONDO_0004907, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006206 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced severe alopecia in inflammatory bowel disease 41 Japanese ancestry cases, 1,179 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 1 alopecia, response to thiopurine http://purl.obolibrary.org/obo/MONDO_0004907, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006207 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced pancreatitis in inflammatory bowel disease 18 Japanese ancestry cases, 1,202 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 2 pancreatitis, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0000278, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006208 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced fever in inflammatory bowel disease 10 Japanese ancestry cases, 1,210 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 0 Fever, response to thiopurine http://purl.obolibrary.org/obo/HP_0001945, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006209 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced digestive symptoms in inflammatory bowel disease 93 Japanese ancestry cases, 1,127 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 1 digestive system disease, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0000405, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006210 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced infection in inflammatory bowel disease 14 Japanese ancestry cases, 1,206 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 0 response to thiopurine, susceptibility to infectious disease measurement http://www.ebi.ac.uk/efo/EFO_0006317, http://www.ebi.ac.uk/efo/EFO_0008422 GCST006211 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced liver dysfunction in inflammatory bowel disease 39 Japanese ancestry cases, 1,181 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 0 response to thiopurine, liver disease http://www.ebi.ac.uk/efo/EFO_0006317, http://www.ebi.ac.uk/efo/EFO_0001421 GCST006212 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced skin symptoms in inflammatory bowel disease 6 Japanese ancestry cases, 1,214 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 0 skin disease, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0000701, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006213 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced alopecia in inflammatory bowel disease (conditioned on rs116855232) 81 Japanese ancestry cases, 1,139 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 0 alopecia, response to thiopurine http://purl.obolibrary.org/obo/MONDO_0004907, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006214 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced acute severe leukopenia in inflammatory bowel disease (conditioned on rs116855232) 43 Japanese ancestry cases, 1,172 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 1 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006215 Genome-wide genotyping array 2018-09-06 29923122 Kakuta Y 2018-06-19 J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/29923122 NUDT15 codon 139 is the best pharmacogenetic marker for predicting thiopurine-induced severe adverse events in Japanese patients with inflammatory bowel disease: a multicenter study. Thiopurine-induced severe alopecia in inflammatory bowel disease (conditioned on rs116855232) 41 Japanese ancestry cases, 1,179 Japanese ancestry controls NA Affymetrix [> 5000000] (imputed) 0 alopecia, response to thiopurine http://purl.obolibrary.org/obo/MONDO_0004907, http://www.ebi.ac.uk/efo/EFO_0006317 GCST006199 Genome-wide genotyping array 2018-05-18 29523850 Gilchrist JJ 2018-03-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29523850 Risk of nontyphoidal Salmonella bacteraemia in African children is modified by STAT4. Nontyphoidal Salmonella bacteraemia 180 Kenyan ancestry cases, 2,677 Kenyan ancestry controls 171 Sub-Saharan African ancestry cases, 563 Sub-Saharan African ancestry controls Affymetrix [at least 4669480] (imputed) 2 non-typhoidal Salmonella bacteremia http://www.ebi.ac.uk/efo/EFO_0009087 GCST005590 Genome-wide genotyping array 2018-05-11 29523524 Singh S 2018-03-09 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29523524 Genome Wide Association Study Identifies the HMGCS2 Locus to be Associated With Chlorthalidone Induced Glucose Increase in Hypertensive Patients. Change in glucose in response to thiazide diuretic treatment in hypertension 135 African American individuals, 175 European ancestry individuals 140 African American individuals, 222 European ancestry individuals Illumina [at least 2500000] (imputed) 6 response to thiazide, glucose measurement http://www.ebi.ac.uk/efo/EFO_0007981, http://www.ebi.ac.uk/efo/EFO_0004468 GCST005577 Genome-wide genotyping array 2018-06-27 29527006 Warrier V 2018-03-12 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29527006 Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa. Empathy quotient 22,318 European ancestry males, 24,543 European ancestry females NA Illumina [9955952] (imputed) 11 empathy measurement http://www.ebi.ac.uk/efo/EFO_0009183 GCST005751 Genome-wide genotyping array 2019-03-04 30626913 Amare AT 2019-01-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30626913 Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. Broad depression or major depressive disorder (self-reported) 9,240 European ancestry broad depression cases, 9,519 European ancestry broad depression controls, 51,258 European ancestry individuals, 75,607 European ancestry self-reported major depressive disorder cases, 231,747 European ancestry self-reported major depressive disorder controls 322,580 individuals Affymetrix, Illumina [at least 918921] (imputed) 3 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST007254 Genome-wide genotyping array 2019-03-04 30626913 Amare AT 2019-01-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30626913 Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. Broad depression or major depressive disorder (recurrent) 9,240 European ancestry broad depression cases, 9,519 European ancestry broad depression controls, 51,258 European ancestry individuals, 5,303 Chinese ancestry recurrent major depressive disorder cases, 5,337 Chinese ancestry recurrent major depressive disorder controls 322,580 individuals Affymetrix, Illumina [at least 918921] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST007256 Genome-wide genotyping array 2019-03-04 30626913 Amare AT 2019-01-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30626913 Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. Broad depression or bipolar disorder 9,240 European ancestry broad depression cases, 9,519 European ancestry broad depression controls, 51,258 European ancestry individuals, 7,481 European ancestry bipolar disorder cases, 9,250 European ancestry bipolar disorder controls 322,580 individuals Affymetrix, Illumina [at least 918921] (imputed) 3 unipolar depression, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985 GCST007255 Genome-wide genotyping array 2019-03-04 30626913 Amare AT 2019-01-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30626913 Bivariate genome-wide association analyses of the broad depression phenotype combined with major depressive disorder, bipolar disorder or schizophrenia reveal eight novel genetic loci for depression. Broad depression or schizophrenia 9,240 European ancestry broad depression cases, 9,519 European ancestry broad depression controls, 51,258 European ancestry individuals, 36,989 European and East Asian ancestry schizophrenia cases, 113,075 European and East Asian ancestry schizophrenia controls 322,580 individuals Affymetrix, Illumina [at least 918921] (imputed) 16 unipolar depression, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0005090 GCST007257 Genome-wide genotyping array 2018-05-08 29520036 Stein MB 2018-03-08 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29520036 Genome-wide analysis of insomnia disorder. Insomnia 2,297 European American cases, 334 African American cases, 606 Latino American cases, 9,176 European American controls, 2,345 African American controls, 2,893 Latino American controls NA Illumina [at least 360704] (imputed) 28 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST005566 Genome-wide genotyping array 2018-07-05 29572449 Gurung RL 2018-03-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29572449 Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians. Urinary haptoglobin levels in type 2 diabetes 236 Chinese ancestry individuals 512 Chinese ancestry individuals, 57 Malay ancestry individuals Illumina [781779] 1 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST005807 Genome-wide genotyping array 2018-07-05 29572449 Gurung RL 2018-03-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29572449 Genetic markers for urine haptoglobin is associated with decline in renal function in type 2 diabetes in East Asians. Plasma haptoglobin levels in type 2 diabetes 236 Chinese ancestry individuals 57 Malay ancestry individuals Illumina [781779] 1 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST005808 Genome-wide genotyping array 2019-08-15 31055733 Nazarian A 2019-05-05 Geroscience www.ncbi.nlm.nih.gov/pubmed/31055733 Genetic heterogeneity of Alzheimer's disease in subjects with and without hypertension. Alzheimer's disease in hypertension-negative individuals 796 European ancestry cases, 4,010 European ancestry controls NA NR [~ 2000000] (imputed) 7 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST008437 Genome-wide genotyping array 2019-08-15 31055733 Nazarian A 2019-05-05 Geroscience www.ncbi.nlm.nih.gov/pubmed/31055733 Genetic heterogeneity of Alzheimer's disease in subjects with and without hypertension. Alzheimer's disease in hypertension 1,262 European ancestry cases, 9,608 European ancestry controls NA NR [~ 2000000] (imputed) 5 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST008438 Genome-wide genotyping array 2018-04-30 26268663 Nalls MA 2015-08-13 Mov Disord www.ncbi.nlm.nih.gov/pubmed/26268663 Baseline genetic associations in the Parkinson's Progression Markers Initiative (PPMI). Parkinson's disease 367 European ancestry typical cases, 55 European ancestry atypical cases, 165 European ancestry controls NA Illumina [> 400000] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST005548 Targeted genotyping array [ImmunoChip, NeuroX] 2017-01-27 27159506 Dunn EC 2016-05-09 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/27159506 Genome-wide association study of generalized anxiety symptoms in the Hispanic Community Health Study/Study of Latinos. Anxiety 12,282 Hispanic ancestry individuals 8,195 Hispanic ancestry individuals Illumina [25568744] (imputed) 0 anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0007795 GCST003562 Genome-wide genotyping array 2018-07-06 29559693 Zengini E 2018-03-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29559693 Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. Osteoarthritis (self-reported) 12,658 European ancestry cases, 50,898 European ancestry controls Affymetrix [16499239] (imputed) 29 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST005811 Genome-wide genotyping array 2018-07-06 29559693 Zengini E 2018-03-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29559693 Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. Osteoarthritis of the hip (hospital diagnosed) 2,396 European ancestry cases, 9,593 European ancestry controls 5,714 Icelandic ancestry cases, 199,421 Icelandic ancestry controls Affymetrix [16122076] (imputed) 5 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST005810 Genome-wide genotyping array 2018-07-06 29559693 Zengini E 2018-03-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29559693 Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. Osteoarthritis (hospital diagnosed) 10,083 European ancestry cases, 40,425 European ancestry controls 18,069 Icelandic ancestry cases, 246,293 Icelandic ancestry controls Affymetrix [16468597] (imputed) 6 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST005814 Genome-wide genotyping array 2018-07-06 29559693 Zengini E 2018-03-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29559693 Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. Osteoarthritis of the knee (hospital diagnosed) 4,462 European ancestry cases, 17,885 European ancestry controls 4,672 Icelandic ancestry cases, 172,791 Icelandic ancestry controls Affymetrix [16309199] (imputed) 7 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST005813 Genome-wide genotyping array 2018-07-06 29559693 Zengini E 2018-03-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29559693 Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis. Osteoarthritis of the hip or knee (hospital diagnosed) 6,586 European ancestry cases, 26,384 European ancestry controls 9,429 Icelandic ancestry cases, 199.421 Icelandic ancestry controls Affymetrix [16396089] (imputed) 8 osteoarthritis, hip, osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616 GCST005812 Genome-wide genotyping array 2018-05-11 29531279 Zhou S 2018-03-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29531279 Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population. Intracranial aneurysm 173 French Canadian cases, 1,772 French Canadian controls 2,617 cases, 1,416 controls Illumina [7614484] (imputed) 31 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST005576 Genome-wide genotyping array 2019-04-18 30617275 Erzurumluoglu AM 2019-01-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30617275 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Smoking initiation 324,851 European ancestry individuals, 21,962 South Asian ancestry individuals up to 275,596 European ancestry individuals Affymetrix, Illumina [up to 1207583] (imputed) 40 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST007603 Genome-wide genotyping array, Exome genotyping array 2019-04-18 30617275 Erzurumluoglu AM 2019-01-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30617275 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Smoking behaviour (cigarettes smoked per day) 128,746 European and South Asian ancestry individuals up to 275,596 European ancestry individuals Affymetrix, Illumina [up to 1207583] (imputed) 8 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST007602 Genome-wide genotyping array, Exome genotyping array 2019-04-18 30617275 Erzurumluoglu AM 2019-01-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30617275 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Smoking behaviour (cigarette pack-years) 131,892 European and South Asian ancestry individuals up to 275,596 European ancestry individuals Affymetrix, Illumina [up to 1207583] (imputed) 0 pack-years measurement http://www.ebi.ac.uk/efo/EFO_0006526 GCST007601 Genome-wide genotyping array, Exome genotyping array 2019-04-18 30617275 Erzurumluoglu AM 2019-01-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30617275 Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci. Smoking cessation 121,543 European and South Asian ancestry individuals up to 275,596 European ancestry individuals Affymetrix, Illumina [up to 1207583] (imputed) 2 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST007604 Genome-wide genotyping array, Exome genotyping array 2018-08-20 29513936 Haasnoot AJW 2018-03-07 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/29513936 An amino acid motif in HLA-DRβ1 distinguishes patients with uveitis in juvenile idiopathic arthritis. Arthritis (juvenile idiopathic) 522 European ancestry JIA cases, 398 European ancestry controls NA Illumina [10051917] (imputed) 0 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST006128 Genome-wide genotyping array 2018-08-20 29513936 Haasnoot AJW 2018-03-07 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/29513936 An amino acid motif in HLA-DRβ1 distinguishes patients with uveitis in juvenile idiopathic arthritis. Uveitis (juvenile idiopathic arthritis-associated) 192 European ancestry JIA-associated uveitis cases, 398 European ancestry controls NA Illumina [10051917] (imputed) 2 uveitis, juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_1001231, http://www.ebi.ac.uk/efo/EFO_0002609 GCST006127 Genome-wide genotyping array 2018-08-20 29513936 Haasnoot AJW 2018-03-07 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/29513936 An amino acid motif in HLA-DRβ1 distinguishes patients with uveitis in juvenile idiopathic arthritis. Uveitis in juvenile idiopathic arthritis 192 European ancestry JIA-associated uveitis cases, 330 European ancestry controls NA Illumina [10051917] (imputed) 0 uveitis http://www.ebi.ac.uk/efo/EFO_1001231 GCST006126 Genome-wide genotyping array 2019-03-18 27089180 Day FR 2016-04-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27089180 Physical and neurobehavioral determinants of reproductive onset and success. Age at first birth 66,310 British ancestry females 117,626 European ancestry males, 144,471 European ancestry females Affymetrix [641018] (imputed) 4 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST007336 Genome-wide genotyping array 2019-03-18 27089180 Day FR 2016-04-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27089180 Physical and neurobehavioral determinants of reproductive onset and success. Age at first sexual intercourse 59,357 British ancestry males, 66,310 British ancestry females NA Affymetrix [641018] (imputed) 36 age at first sexual intercourse measurement http://www.ebi.ac.uk/efo/EFO_0009749 GCST007335 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Myeloid white cell count 169,219 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 164 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST004626 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Lymphocyte count 171,643 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 188 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST004627 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Immature fraction of reticulocytes 170,548 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 152 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST004628 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Neutrophil count 170,702 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 152 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST004629 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Mean corpuscular hemoglobin 172,332 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 275 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST004630 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Basophil percentage of white cells 171,996 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 65 basophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007992 GCST004631 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Lymphocyte percentage of white cells 171,748 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 147 lymphocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007993 GCST004632 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Neutrophil percentage of white cells 171,542 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 135 neutrophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007990 GCST004633 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Basophil percentage of granulocytes 170,223 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 62 basophil percentage of granulocytes http://www.ebi.ac.uk/efo/EFO_0007995 GCST004634 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Mean platelet volume 164,454 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 294 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST004599 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Red blood cell count 172,952 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 212 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST004601 Genome-wide genotyping array 2017-05-12 27992413 Ji SG 2016-12-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27992413 Genome-wide association study of primary sclerosing cholangitis identifies new risk loci and quantifies the genetic relationship with inflammatory bowel disease. Primary sclerosing cholangitis 2,871 European ancestry cases, 12,019 European ancestry controls 1,925 European ancestry cases, 7,936 European ancestry controls Affymetrix, Illumina [7891602] (imputed) 30 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST004030 Genome-wide genotyping array 2017-03-10 27094239 Joshi AD 2016-04-16 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/27094239 Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies. Gallstone disease 8,720 European ancestry cases, 55,152 European ancestry controls 6,489 European ancestry cases, 62,797 European ancestry controls, 1,499 African American cases, 9,145 African American controls, 1,056 Hispanic cases, 2,403 Hispanic controls Affymetrix, Illumina [at least 2305318] (imputed) 6 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST003725 Genome-wide genotyping array 2017-03-28 27980656 Justice AE 2016-10-18 BMC Proc www.ncbi.nlm.nih.gov/pubmed/27980656 Genome-wide association of trajectories of systolic blood pressure change. Systolic blood pressure change trajectory up to 683 Mexican American individuals from 20 families NA Illumina [at least 472049] (imputed) 10 systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006944 GCST003825 Genome-wide genotyping array 2017-03-24 26965516 Zeng C 2016-03-08 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/26965516 Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk. Colorectal cancer 4,508 East Asian ancestry cases, 16,588 East Asian ancestry controls 11,044 East Asian ancestry cases, 18,036 East Asian ancestry controls Affymetrix, Illumina [~ 4000000] (imputed) 30 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST003799 Genome-wide genotyping array 2017-06-27 28292921 Boldry EJ 2017-03-14 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28292921 Genetic Determinants of 1,3-Butadiene Metabolism and Detoxification in Three Populations of Smokers with Different Risks of Lung Cancer. Urinary 1,3-butadiene metabolite levels in smokers 327 African American individuals, 349 Japanese American individuals, 396 European ancestry individuals NA Illumina [11892802] (imputed) 4 urinary 1,3-butadiene measurement http://www.ebi.ac.uk/efo/EFO_0007957 GCST004254 Genome-wide genotyping array 2017-04-21 27993963 Schneider BP 2016-12-19 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/27993963 Genome-Wide Association Study for Anthracycline-Induced Congestive Heart Failure. Adverse response to chemotherapy (congestive heart failure) in breast cancer 51 European American ancestry cases, 794 European American ancestry controls 21 European ancestry cases, 266 European ancestry controls Illumina [810907] (imputed) 0 response to bevacizumab, congestive heart failure, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_0005943, http://www.ebi.ac.uk/efo/EFO_0000373, http://www.ebi.ac.uk/efo/EFO_0005257 GCST003939 Genome-wide genotyping array 2017-06-30 28333968 Nielsen TR 2017-03-23 PLoS One www.ncbi.nlm.nih.gov/pubmed/28333968 A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents. Plasma thyroid-stimulating hormone levels 1,680 Danish ancestry children and adolescents 2,129 Danish ancestry children and adolescents Illumina [8508717] (imputed) 7 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST004276 Genome-wide genotyping array 2017-06-30 28333968 Nielsen TR 2017-03-23 PLoS One www.ncbi.nlm.nih.gov/pubmed/28333968 A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents. Free thyroxine concentration 1,680 Danish ancestry children and adolescents 2,129 Danish ancestry children and adolescents Illumina [8508717] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST004277 Genome-wide genotyping array 2017-07-03 28375557 Thomsen H 2017-04-04 Eur J Haematol www.ncbi.nlm.nih.gov/pubmed/28375557 Genomewide association study on monoclonal gammopathy of unknown significance (MGUS). Monoclonal gammopathy of undetermined significance 243 German ancestry cases and 1285 German ancestry controls 294 cases and 272 controls Illumina [NR] 0 monoclonal gammopathy http://www.ebi.ac.uk/efo/EFO_0000203 GCST004287 Genome-wide genotyping array 2017-06-12 28334792 Nongmaithem SS 2017-02-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334792 GWAS identifies population-specific new regulatory variants in FUT6 associated with plasma B12 concentrations in Indians. Vitamin B12 levels 1,001 Indo-European ancestry adults 1,713 Indo-European ancestry adults, 690 Indo-European ancestry children, 481 Dravidian ancestry adults, 534 Dravidian ancestry children Affymetrix [8900000] (imputed) 4 vitamin B12 measurement http://www.ebi.ac.uk/efo/EFO_0004620 GCST004161 Genome-wide genotyping array 2017-07-13 28374850 Ellinghaus E 2017-04-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28374850 Genome-wide association analysis for chronic venous disease identifies EFEMP1 and KCNH8 as susceptibility loci. Chronic venous disease 323 German ancestry cases and 4,619 German ancestry controls 1,946 German ancestry cases and 3,146 German ancestry controls Affymetrix [1934349] (imputed) 3 chronic venous insufficiency, Varicose veins http://www.ebi.ac.uk/efo/EFO_0007940, http://purl.obolibrary.org/obo/HP_0002619 GCST004343 Genome-wide genotyping array 2017-08-07 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Low-grade serous and serous borderline ovarian cancer 2,966 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 12 ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_1001516 GCST004481 Genome-wide genotyping array 2017-08-03 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Ovarian cancer in BRCA2 mutation carriers 954 European ancestry carrier cases, 11,458 European ancestry carrier controls NA Illumina [11595112] (imputed) 2 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST004416 Genome-wide genotyping array 2017-08-04 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Epithelial ovarian cancer 16,924 European ancestry cases, 68,502 European ancestry controls NA Illumina [11595112] (imputed) 23 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST004462 Genome-wide genotyping array 2017-08-03 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Ovarian clear cell cancer 1,366 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 2 ovarian clear cell adenocarcinoma http://www.ebi.ac.uk/efo/EFO_1000042 GCST004417 Genome-wide genotyping array 2017-08-03 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Endometrioid ovarian cancer 2,810 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 1 ovarian endometrioid carcinoma http://www.ebi.ac.uk/efo/EFO_1001515 GCST004418 Genome-wide genotyping array 2017-08-03 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Mucinous ovarian carcinoma 2,566 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 7 ovarian mucinous adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0006462 GCST004419 Genome-wide genotyping array 2017-08-07 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Serous invasive ovarian cancer 14,049 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 21 ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_1001516 GCST004478 Genome-wide genotyping array 2017-08-07 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Serous borderline ovarian cancer 1,954 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 10 ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_1001516 GCST004479 Genome-wide genotyping array 2017-08-07 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. High-grade serous ovarian cancer 13,037 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 21 ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_1001516 GCST004480 Genome-wide genotyping array 2017-08-04 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Low-grade serous ovarian cancer 1,012 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 1 ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_1001516 GCST004461 Genome-wide genotyping array 2017-08-03 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Ovarian cancer in BRCA1 mutation carriers 2,933 European ancestry carrier cases, 16,103 European ancestry carrier controls NA Illumina [11595112] (imputed) 4 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST004414 Genome-wide genotyping array 2017-08-03 28346442 Phelan CM 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346442 Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer. Invasive epithelial ovarian cancer 22,406 European ancestry cases, 40,941 European ancestry controls NA Illumina [11595112] (imputed) 19 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST004415 Genome-wide genotyping array 2017-06-01 28056976 Paziewska A 2017-01-06 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/28056976 A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients. Primary biliary cholangitis 443 Polish ancestry cases, 934 Polish ancestry controls NA Illumina [NR] 0 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST004120 Genome-wide genotyping array 2017-06-01 28056976 Paziewska A 2017-01-06 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/28056976 A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients. Primary sclerosing cholangitis 120 Polish ancestry cases, 934 Polish ancestry controls NA Illumina [NR] 0 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST004119 Genome-wide genotyping array 2017-06-28 28373160 Klarin D 2017-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28373160 Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor. Venous thromboembolism 3,290 European ancestry cases, 116,868 European ancestry controls 65,734 cases and controls (see Germain, 2015) Affymetrix [9155762] (imputed) 9 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST004256 Genome-wide genotyping array 2019-10-21 31174203 Liyanage UE 2019-06-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31174203 Combined analysis of keratinocyte cancers identifies novel genome-wide loci. Keratinocyte cancer (MTAG) at least 18,538 European ancestry cases, at least 340,302 European ancestry controls NA Affymetrix [7600000] (imputed) 88 keratinocyte carcinoma http://www.ebi.ac.uk/efo/EFO_0010176 GCST008870 Genome-wide genotyping array 2019-10-21 31174203 Liyanage UE 2019-06-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31174203 Combined analysis of keratinocyte cancers identifies novel genome-wide loci. Basal cell carcinoma 31,787 European ancestry cases, 619,351 European ancestry controls NA Affymetrix, Illumina [up to 9061544] (imputed) 76 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST008871 Genome-wide genotyping array 2019-10-21 31174203 Liyanage UE 2019-06-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31174203 Combined analysis of keratinocyte cancers identifies novel genome-wide loci. Squamous cell carcinoma 9,674 European ancestry cases, 625,657 European ancestry controls NA Affymetrix, Illumina [up to 9061544] (imputed) 21 squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707 GCST008872 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (language ability) 488 European ancestry single-episode cases, 533 European ancestry recurrent episode cases, 5,991 European ancestry controls NA Illumina [557292] 0 cognitive function measurement, language measurement http://www.ebi.ac.uk/efo/EFO_0008354, http://www.ebi.ac.uk/efo/EFO_0007797 GCST008587 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (processing speed) x major depressive disorder status interaction 533 European ancestry recurrent episode cases, 5,991 European ancestry controls NA Illumina [557292] 0 unipolar depression, information processing speed, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0008354 GCST008583 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (language ability) x major depressive disorder status interaction 488 European ancestry single-episode cases, 533 European ancestry recurrent episode cases, 5,991 European ancestry controls NA Illumina [557292] 0 unipolar depression, cognitive function measurement, language measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354, http://www.ebi.ac.uk/efo/EFO_0007797 GCST008584 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (language ability) x major depressive disorder status interaction 533 European ancestry recurrent episode cases, 5,991 European ancestry controls NA Illumina [557292] 0 unipolar depression, cognitive function measurement, language measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354, http://www.ebi.ac.uk/efo/EFO_0007797 GCST008585 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (processing speed) x major depressive disorder type interaction 488 European ancestry single-episode cases, 533 European ancestry recurrent episode cases NA Illumina [557292] 0 unipolar depression, information processing speed, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0008354 GCST008586 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (language ability) 533 European ancestry recurrent episode cases, 5,991 European ancestry controls NA Illumina [557292] 0 cognitive function measurement, language measurement http://www.ebi.ac.uk/efo/EFO_0008354, http://www.ebi.ac.uk/efo/EFO_0007797 GCST008588 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (processing speed) in major depressive disorder 488 European ancestry single-episode cases, 533 European ancestry recurrent episode cases NA Illumina [557292] 0 information processing speed, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0008354 GCST008589 Genome-wide genotyping array 2019-09-03 29531327 Meijsen JJ 2018-03-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29531327 Phenotypic and genetic analysis of cognitive performance in Major Depressive Disorder in the Generation Scotland: Scottish Family Health Study. Cognitive performance (processing speed) 533 European ancestry recurrent episode cases, 5,991 European ancestry controls NA Illumina [557292] 0 information processing speed, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0008354 GCST008590 Genome-wide genotyping array 2018-05-02 29534260 Kim SK 2018-03-13 Int J Sports Med www.ncbi.nlm.nih.gov/pubmed/29534260 Two Genetic Variants Associated with Plantar Fascial Disorders. Plantar fascial disorders 17,627 European ancestry cases, 2,044 Latin American cases, 1,300 East Asian cases, 658 African American cases, 65,637 European ancestry controls, 6,516 Latin American controls, 6,218 East Asian controls, 2,508 African American controls NA Affymetrix [9322588] (imputed) 2 Plantar Fasciitis, Plantar Fibromatosis http://www.ebi.ac.uk/efo/EFO_1001909, http://www.ebi.ac.uk/efo/EFO_1000481 GCST005558 Genome-wide genotyping array 2018-02-09 29263008 Guerreiro R 2018-01-01 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29263008 Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study. Dementia with Lewy bodies 1,216 European ancestry cases, 3,791 European ancestry controls 527 European ancestry cases, 663 European ancestry controls Illumina [8397716] (imputed) 4 Lewy body dementia http://www.ebi.ac.uk/efo/EFO_0006792 GCST005276 Genome-wide genotyping array 2019-02-07 29768301 Ingle JN 2018-06-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/29768301 Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab. Disease-free survival in breast cancer treated with chemotherapy with or without bevacizumab 890 cases 1,398 cases Illumina [> 7000000] (imputed) 0 disease free survival, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0000409, http://purl.obolibrary.org/obo/GO_0097327 GCST007046 Genome-wide genotyping array 2019-02-07 29768301 Ingle JN 2018-06-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/29768301 Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab. Overall survival in breast cancer treated with chemotherapy with or without bevacizumab 891 cases 1,398 individuals Illumina [> 7000000] (imputed) 0 overall survival, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0000638, http://purl.obolibrary.org/obo/GO_0097327 GCST007049 Genome-wide genotyping array 2019-02-07 29768301 Ingle JN 2018-06-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/29768301 Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab. Pathological complete response in breast cancer treated with chemotherapy with bevacizumab 147 cases with pathological complete response, 300 cases without pathological complete response 142 cases with pathological complete response, 591 cases without pathological complete response Illumina [> 7000000] (imputed) 0 response to bevacizumab, pathologic complete response measurement, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0005943, http://www.ebi.ac.uk/efo/EFO_0007771, http://purl.obolibrary.org/obo/GO_0097327 GCST007048 Genome-wide genotyping array 2019-02-07 29768301 Ingle JN 2018-06-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/29768301 Germline genome-wide association studies in women receiving neoadjuvant chemotherapy with or without bevacizumab. Pathological complete response in breast cancer treated with or without bevacizumab 236 cases with pathological complete response, 678 cases without pathological complete response 254 cases with pathological complete response, 1,144 cases without pathological complete response Illumina [> 7000000] (imputed) 0 pathologic complete response measurement, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0007771, http://purl.obolibrary.org/obo/GO_0097327 GCST007047 Genome-wide genotyping array 2017-09-25 28776448 Beaudoin JJ 2017-08-04 Scand J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/28776448 An exploratory genome-wide analysis of genetic risk for alcoholic hepatitis. Alcoholic hepatitis 90 European ancestry heavy drinking cases, 93 European ancestry heavy drinking controls NA Illumina [819401] 0 Hepatitis, Alcoholic http://www.ebi.ac.uk/efo/EFO_1001345 GCST004784 Genome-wide genotyping array 2018-02-01 29255261 Luciano M 2017-12-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29255261 Association analysis in over 329,000 individuals identifies 116 independent variants influencing neuroticism. Neuroticism 329,821 European ancestry individuals 122,867 European ancestry individuals Illumina [18485882] (imputed) 166 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST005232 Genome-wide genotyping array 2016-12-21 27145994 Wang M 2016-05-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27145994 Common genetic variation in ETV6 is associated with colorectal cancer susceptibility. Colorectal cancer 1,023 Han Chinese ancestry cases and 1,306 Han Chinese ancestry controls 5,317 Han Chinese ancestry cases, 6,887 Han Chinese ancestry controls, 1,046 European ancestry cases, 1,076 European ancestry controls Illumina [691326] 4 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST003494 Genome-wide genotyping array 2018-08-03 29031612 Hirata J 2017-10-12 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/29031612 Variants at HLA-A, HLA-C, and HLA-DQB1 Confer Risk of Psoriasis Vulgaris in Japanese. Psoriasis vulgaris 282 Japanese ancestry cases, 426 Japanese ancestry controls 320 Japanese ancestry cases, 1,622 Japanese ancestry controls Illumina [6369185] (imputed) 2 psoriasis vulgaris http://www.ebi.ac.uk/efo/EFO_1001494 GCST006036 Genome-wide genotyping array 2019-08-08 25861811 Li Z 2015-04-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25861811 A common variant near TGFBR3 is associated with primary open angle glaucoma. Glaucoma (primary open-angle) 2,735 East Asian ancestry cases, 590 African American cases, 121 South Asian ancestry cases, 58 South East Asian ancestry cases, 6,410 East Asian ancestry controls, 636 African American controls, 716 South Asian ancestry controls, 1,984 South East Asian ancestry controls 4,773 European ancestry cases, 3,006 East Asian ancestry cases, 497 African American cases, 453 South Asian ancestry cases, 208 South East Asian ancestry cases, 236 Middle East ancestry cases, 11,786 European ancestry controls, 8,754 East Asian ancestry controls, 304 African American controls, 2,496 South Asian ancestry controls, 2,785 South East Asian ancestry controls, 655 Middle East ancestry controls Illumina [~ 272000] 4 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST008391 Exome genotyping array [Exome array] 2018-02-22 29309628 Beaumont RN 2018-01-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29309628 Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics. Offspring birth weight 68,258 European ancestry women 18,319 European ancestry women Affymetrix, Illumina, Perlegen [up to 8741107] (imputed) 2 birth weight, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005314 Genome-wide genotyping array 2018-01-30 29266176 Inaba H 2017-12-19 Cancer www.ncbi.nlm.nih.gov/pubmed/29266176 Bone mineral density in children with acute lymphoblastic leukemia. Bone mineral density change response to combined chemotherapy in acute lymphoblastic leukemia 235 European ancestry cases, 48 African American ancestry cases, 13 cases NA Affymetrix [448281] 4 spine bone mineral density change measurement, response to combination chemotherapy http://www.ebi.ac.uk/efo/EFO_0008474, http://www.ebi.ac.uk/efo/EFO_0007965 GCST005214 Genome-wide genotyping array 2018-07-24 29868224 Sallah N 2017-11-27 Glob Health Epidemiol Genom www.ncbi.nlm.nih.gov/pubmed/29868224 Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot. Epstein Barr virus nuclear antigen 1 IgG levels 1,473 Ugandan ancestry individuals, 2,162 European ancestry individuals NA Illumina [up to 17000000] (imputed) 2 Epstein Barr virus nuclear antigen 1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0007790 GCST005963 Genome-wide genotyping array, Genome-wide sequencing 2018-07-23 29868224 Sallah N 2017-11-27 Glob Health Epidemiol Genom www.ncbi.nlm.nih.gov/pubmed/29868224 Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot. Epstein Barr virus nuclear antigen 1 IgG seropositivity 1,201 Ugandan ancestry cases, 361 Ugandan ancestry controls NA Illumina [~ 17000000] (imputed) 1 Epstein Barr virus nuclear antigen-1 seropositivity http://www.ebi.ac.uk/efo/EFO_0009271 GCST005941 Genome-wide genotyping array, Genome-wide sequencing 2018-07-23 29868224 Sallah N 2017-11-27 Glob Health Epidemiol Genom www.ncbi.nlm.nih.gov/pubmed/29868224 Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot. Viral capsid antigen IgG levels 1,473 Ugandan ancestry individuals NA Illumina [~ 17000000] (imputed) 0 Epstein Barr viral capsid antigen IgG measurement http://www.ebi.ac.uk/efo/EFO_0009274 GCST005942 Genome-wide genotyping array, Genome-wide sequencing 2018-07-23 29868224 Sallah N 2017-11-27 Glob Health Epidemiol Genom www.ncbi.nlm.nih.gov/pubmed/29868224 Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot. Viral capsid antigen IgG seropositivity 1,344 Ugandan ancestry cases, 218 Ugandan ancestry controls NA Illumina [~ 17000000] (imputed) 4 Epstein Barr viral capsid antigen seropositivity http://www.ebi.ac.uk/efo/EFO_0009272 GCST005944 Genome-wide genotyping array, Genome-wide sequencing 2018-07-23 29868224 Sallah N 2017-11-27 Glob Health Epidemiol Genom www.ncbi.nlm.nih.gov/pubmed/29868224 Whole-genome association study of antibody response to Epstein-Barr virus in an African population: a pilot. Epstein-Barr virus immune response (multivariate analysis) 1,473 Ugandan ancestry individuals NA Illumina [~ 17000000] (imputed) 1 anti-Epstein Barr virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0009273 GCST005943 Genome-wide genotyping array, Genome-wide sequencing 2018-07-04 29425463 Bime C 2018-02-09 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/29425463 Genome Wide Association Study in African Americans with Acute Respiratory Distress Syndrome Identifies the Selectin P Ligand Gene as a Risk Factor. Acute respiratory distress syndrome 232 African American ancestry cases, 162 African American ancestry controls with sepsis or other risk factors 140 African American cases, 269 European ancestry cases, 222 African American ancestry controls with sepsis, 338 European ancestry controls with sepsis Affymetrix [1428996] 0 acute respiratory distress syndrome http://www.ebi.ac.uk/efo/EFO_1000637 GCST005805 Genome-wide genotyping array 2018-01-18 29263402 Han Y 2017-12-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29263402 Genome-wide association study identifies a missense variant at APOA5 for coronary artery disease in Multi-Ethnic Cohorts from Southeast Asia. Coronary artery disease 1,778 Chinese ancestry cases, 391 Malay ancestry cases, 5,164 Chinese ancestry controls, 2,212 Malay ancestry controls 291 Asian Indian cases, 1,848 Asian Indian controls Illumina [at least 5827330] (imputed) 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST005172 Genome-wide genotyping array 2018-09-06 25817017 Carmona FD 2015-03-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25817017 A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility. Giant cell arteritis 1,651 European ancestry cases, 15,306 European ancestry controls NA Illumina [95416] 3 temporal arteritis http://www.ebi.ac.uk/efo/EFO_1001209 GCST006198 Targeted genotyping array [ImmunoChip] 2016-11-30 27206850 Wang M 2016-03-29 Cancer Res www.ncbi.nlm.nih.gov/pubmed/27206850 Genome-Wide Association Study of Bladder Cancer in a Chinese Cohort Reveals a New Susceptibility Locus at 5q12.3. Bladder cancer 578 Han Chinese ancestry cases, 1,006 Han Chinese ancestry controls 2,828 Han Chinese ancestry cases, 3,639 Han Chinese ancestry controls Illumina [478403] (imputed) 1 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST003384 Genome-wide genotyping array 2017-10-23 28952330 Chen SP 2017-01-01 Cephalalgia www.ncbi.nlm.nih.gov/pubmed/28952330 Genome-wide association study identifies novel susceptibility loci for migraine in Han Chinese resided in Taiwan. Migraine without aura 1,005 Han Chinese ancestry cases, 1,053 Han Chinese ancestry controls 1,120 Han Chinese ancestry cases, 604 Han Chinese ancestry controls Affymetrix [590945] 2 migraine without aura, susceptibility to, 4 http://purl.obolibrary.org/obo/MONDO_0011847 GCST004900 Genome-wide genotyping array 2018-04-06 29422604 Klein AP 2018-02-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29422604 Genome-wide meta-analysis identifies five new susceptibility loci for pancreatic cancer. Pancreatic cancer 9,040 European ancestry cases, 12,496 European ancestry controls up to 2,737 cases, up to 4,752 controls Illumina [11381182] (imputed) 32 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST005434 Genome-wide genotyping array 2018-09-20 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. Cholesterol, total 1,017 Yoruban ancestry individuals, 1,765 Filipino ancestry individuals NA Affymetrix, Illumina [up to 12553142] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST006305 Genome-wide genotyping array 2018-09-20 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. HDL cholesterol 1,017 Yoruban ancestry individuals, 1,765 Filipino ancestry individuals NA Affymetrix, Illumina [up to 12553142] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST006306 Genome-wide genotyping array 2018-09-20 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. LDL cholesterol 1,017 Yoruban ancestry individuals, 1,765 Filipino ancestry individuals NA Affymetrix, Illumina [up to 12553142] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST006307 Genome-wide genotyping array 2018-09-20 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. Triglycerides 1,017 Yoruban ancestry individuals, 1,765 Filipino ancestry individuals NA Affymetrix, Illumina [up to 12553142] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST006308 Genome-wide genotyping array 2018-10-24 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. Cholesterol, total 1,017 Yoruban ancestry individuals,1,765 Filipino ancestry individuals 188,577 European and other ancestry individuals Illumina [4454201] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST006469 Targeted genotyping array [XBEP method] 2018-10-24 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. HDL cholesterol 1,017 Yoruban ancestry individuals, 1,765 Filipino ancestry individuals 188,577 European and other ancestry individuals Illumina [4454201] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST006470 Targeted genotyping array [XBEP method] 2018-10-24 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. LDL cholesterol 1,017 Yoruban ancestry individuals, 1,765 Filipino ancestry individuals 188,577 European and other ancestry individuals Illumina [4454201] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST006471 Targeted genotyping array [XBEP method] 2018-10-24 29404214 Andaleon A 2018-01-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/29404214 Gene-based association study for lipid traits in diverse cohorts implicates BACE1 and SIDT2 regulation in triglyceride levels. Triglyceride levels 1,017 Yoruban ancestry individuals, 1,765 Filipino individuals 188,577 European and other ancestry individuals Illumina [4454201] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST006472 Targeted genotyping array [XBEP method] 2018-03-29 29394082 Burkart KM 2018-02-02 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/29394082 A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos. FEV1 11,822 Hispanic individuals up to 4,162 Hispanic individuals, up to 876 African American individuals, up to 94,612 European ancestry individuals Illumina [27887661] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST005418 Genome-wide genotyping array 2018-03-29 29394082 Burkart KM 2018-02-02 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/29394082 A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos. Lung function (FEV1/FVC) 11,822 Hispanic individuals up to 4,162 Hispanic individuals, up to 876 African American individuals, up to 94,612 European ancestry individuals Illumina [2232944] (imputed) 3 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST005419 Genome-wide genotyping array 2018-03-29 29394082 Burkart KM 2018-02-02 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/29394082 A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos. Airflow obstruction 854 Hispanic cases, 9,549 Hispanic controls European ancestry individuals (see Wilk et al 2012) Illumina [up to 27887661] (imputed) 1 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST005416 Genome-wide genotyping array 2018-03-29 29394082 Burkart KM 2018-02-02 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/29394082 A Genome-wide Association Study in Hispanics/Latinos Identifies Novel Signals for Lung Function. The Hispanic Community Health Study/Study of Latinos. Chronic obstructive pulmonary disease 363 Hispanic cases, 5,253 Hispanic controls European ancestry cases and controls (see Wilk et al 2012) Illumina [up to 27887661] (imputed) 2 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST005417 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. Intracranial haemorrhage in renal transplantation (donors) 1,304 European ancestry donor cases, 8,784 European ancestry donor, recipient and other controls 2,407 European ancestry donor cases, 2,620 European ancestry donor controls Illumina [NR] 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST005426 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. End stage renal failure in renal transplantation (recipient effect) 2,689 European ancestry recipient cases, 7,399 European ancestry donor and other controls 5,866 European ancestry individuals Illumina [NR] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST005427 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. Graft survival time in renal transplantation (recipient effect) up to 2,689 European ancestry individuals 5,866 European ancestry individuals Illumina [NR] 0 renal transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005199 GCST005428 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. Graft survival time in renal transplantation (donor effect) up to 2,204 European ancestry donors 5,027 European ancestry donors Illumina [NR] 0 renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST005429 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. Graft survival time in renal transplantation (donor-recipient interaction) 2,094 European ancestry donor-recipient pairs 5,866 European ancestry donor-recipient pairs Illumina [NR] 0 renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST005430 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. Acute graft rejection in renal transplantation (recipient effect) 441 European ancestry cases, 941 European ancestry controls 575 European ancestry cases, 2,573 European ancestry controls Illumina [NR] 0 renal transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005199 GCST005431 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. Acute graft rejection in renal transplantation (donor effect) 414 European ancestry donors (rejection outcome), 825 European ancestry donors (no rejection outcome) 575 European ancestry donors (rejection outcome), 2,573 European ancestry donors (no rejection outcome) Illumina [NR] 0 renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST005432 Genome-wide genotyping array 2018-04-04 29392897 Hernandez-Fuentes MP 2018-02-01 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/29392897 Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study. Acute graft rejection in renal transplantation (donor-recipient interaction) 343 European ancestry recipient-donor pair cases, 755 European ancestry recipient-donor pair controls 575 European ancestry recipient-donor pair cases, 2,573 European ancestry recipient-donor pair controls Illumina [NR] 0 renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST005433 Genome-wide genotyping array 2018-01-12 29146897 Pirastu N 2017-11-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29146897 GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk. Male-pattern baldness 25,662 British ancestry cases, 17,928 British ancestry controls 13,367 European ancestry cases, 11,851 European ancestry controls, 3,436 cases, 2,435 controls Affymetrix [27512692] (imputed) 58 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST005116 Genome-wide genotyping array 2017-11-30 29057527 Ballantine JL 2017-10-23 Int J Paediatr Dent www.ncbi.nlm.nih.gov/pubmed/29057527 Exploring the genomic basis of early childhood caries: a pilot study. Early childhood caries 26 African American cases, 34 Hispanic cases, 13 European ancestry cases, 6 Native-American ancestry cases, 1 case, 41 African American controls, 40 Hispanic controls, 36 European ancestry controls, 15 Native-American ancestry controls. 265 cases, 656 controls Illumina [~ 1400000] 0 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST004989 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Total cholesterol levels 128,305 Japanese ancestry individuals NA Illumina [6108953] (imputed) 45 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST006034 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. White blood cell count 107,964 Japanese ancestry individuals NA Illumina [6108953] (imputed) 42 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST005973 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Neutrophil count 62,076 Japanese ancestry individuals NA Illumina [6108953] (imputed) 22 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST005974 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Eosinophil counts 62,076 Japanese ancestry individuals NA Illumina [6108953] (imputed) 20 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST005975 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. White blood cell count (basophil) 62,076 Japanese ancestry individuals NA Illumina [6108953] (imputed) 28 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST005976 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Monocyte count 62,076 Japanese ancestry individuals NA Illumina [6108953] (imputed) 34 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST005977 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Lymphocyte count 62,076 Japanese ancestry individuals NA Illumina [6108953] (imputed) 14 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST005997 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Red blood cell count 108,794 Japanese ancestry individuals NA Illumina [6108953] (imputed) 60 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST005996 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Hemoglobin 108,769 Japanese ancestry individuals NA Illumina [6108953] (imputed) 20 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST005995 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Hematocrit 108,757 Japanese ancestry individuals NA Illumina [6108953] (imputed) 23 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST005994 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Mean corpuscular volume 108,256 Japanese ancestry individuals NA Illumina [6108953] (imputed) 111 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST006011 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Mean corpuscular hemoglobin 108,054 Japanese ancestry individuals NA Illumina [6108953] (imputed) 96 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST005993 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Mean corpuscular hemoglobin concentration 108,728 Japanese ancestry individuals NA Illumina [6108953] (imputed) 44 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST005992 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Platelet count 108,208 Japanese ancestry individuals NA Illumina [6108953] (imputed) 96 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST005991 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Non-albumin protein levels 98,538 Japanese ancestry individuals NA Illumina [6108953] (imputed) 58 serum non-albumin protein measurement http://www.ebi.ac.uk/efo/EFO_0004568 GCST005990 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Serum total protein levels 113,509 Japanese ancestry individuals NA Illumina [6108953] (imputed) 39 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST005989 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Serum albumin levels 102,223 Japanese ancestry individuals NA Illumina [6108953] (imputed) 17 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST005988 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Albumin-globulin ratio 98,626 Japanese ancestry individuals NA Illumina [6108953] (imputed) 50 albumin:globulin ratio measurement http://www.ebi.ac.uk/efo/EFO_0005128 GCST005987 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Blood urea nitrogen levels 139,818 Japanese ancestry individuals NA Illumina [6108953] (imputed) 44 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST005986 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Creatinine levels 142,097 Japanese ancestry individuals NA Illumina [6108953] (imputed) 68 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST005985 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Glomerular filtration rate 143,658 Japanese ancestry individuals NA Illumina [6108953] (imputed) 72 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST005984 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Serum uric acid levels 109,029 Japanese ancestry individuals NA Illumina [6108953] (imputed) 48 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST005983 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Sodium levels 127,304 Japanese ancestry individuals NA Illumina [6108953] (imputed) 14 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST006032 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Potassium levels 132,938 Japanese ancestry individuals NA Illumina [6108953] (imputed) 15 potassium measurement http://www.ebi.ac.uk/efo/EFO_0009283 GCST006031 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Chloride levels 126,402 Japanese ancestry individuals NA Illumina [6108953] (imputed) 19 chloride measurement http://www.ebi.ac.uk/efo/EFO_0009284 GCST006030 Genome-wide genotyping array 2018-04-25 24076602 Beecham AH 2013-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24076602 Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Multiple sclerosis 14,498 European ancestry cases, 24,091 European ancestry controls 14,802 European ancestry cases, 26,703 European ancestry controls Illumina [161311] 126 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST005531 Targeted genotyping array [ImmunoChip] 2017-02-10 27558924 Kim HS 2016-08-24 Gut www.ncbi.nlm.nih.gov/pubmed/27558924 A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD. Thiopurine-induced leukopenia in inflammatory bowel disease 113 Korean ancestry cases, 154 Korean ancestry controls 245 East Asian ancestry cases, 522 East Asian ancestry controls Affymetrix [505014] 2 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST003603 Genome-wide genotyping array 2017-11-08 28983962 Cheung JPY 2017-10-06 J Orthop Res www.ncbi.nlm.nih.gov/pubmed/28983962 Etiology of developmental spinal stenosis: A genome-wide association study. Lumbar spinal stenosis 469 Chinese ancestry individuals NA Illumina [~ 800000] 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST004945 Genome-wide genotyping array 2017-02-23 27560520 Shaffer JR 2016-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27560520 Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Cranial base width 2,447 European ancestry individuals 671 European ancestry individuals Illumina [34985077] (imputed) 4 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST003641 Genome-wide genotyping array 2017-02-23 27560520 Shaffer JR 2016-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27560520 Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Eye morphology 2,447 European ancestry individuals 671 European ancestry individuals Illumina [34985077] (imputed) 5 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST003642 Genome-wide genotyping array 2017-02-23 27560520 Shaffer JR 2016-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27560520 Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Nose morphology 2,447 European ancestry individuals 671 European ancestry individuals Illumina [34985077] (imputed) 8 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST003643 Genome-wide genotyping array 2017-02-23 27560520 Shaffer JR 2016-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27560520 Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Lip morphology 2,447 European ancestry individuals 671 European ancestry individuals Illumina [34985077] (imputed) 5 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST003644 Genome-wide genotyping array 2017-02-23 27560520 Shaffer JR 2016-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27560520 Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Lower facial height 2,447 European ancestry individuals 671 European ancestry individuals Illumina [34985077] (imputed) 2 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST003645 Genome-wide genotyping array 2017-02-23 27560520 Shaffer JR 2016-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27560520 Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology. Facial depth 2,447 European ancestry individuals 671 European ancestry individuals Illumina [34985077] (imputed) 7 facial depth measurement http://www.ebi.ac.uk/efo/EFO_0007857 GCST003646 Genome-wide genotyping array 2017-02-19 27559109 Bustamante M 2016-08-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27559109 A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. diarrhoeal disease at age 1 2,693 European ancestry cases, 3,065 European ancestry controls 2,302 European ancestry cases, 1,466 European ancestry controls Illumina [at least 5400000] (imputed) 1 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST003626 Genome-wide genotyping array 2017-02-19 27559109 Bustamante M 2016-08-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27559109 A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. diarrhoeal disease at age 1 with doctor diagnosis 1,339 European ancestry cases, 5,064 European ancestry controls 1,411 European ancestry cases, 6,054 European ancestry controls Affymetrix, Illumina [at least 5400000] (imputed) 1 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST003625 Genome-wide genotyping array 2017-02-19 27559109 Bustamante M 2016-08-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27559109 A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. diarrhoeal disease at age 2 2,855 European ancestry cases, 2,753 European ancestry controls 1,972 European ancestry cases, 1,544 European ancestry controls Illumina [at least 5400000] (imputed) 1 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST003623 Genome-wide genotyping array 2017-02-19 27559109 Bustamante M 2016-08-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27559109 A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways. diarrhoeal disease at age 2 with doctor diagnosis 990 European ancestry cases, 5,243 European ancestry controls 1,274 European ancestry cases, 6,448 European ancestry controls Affymetrix, Illumina [at least 5400000] (imputed) 1 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST003624 Genome-wide genotyping array 2017-10-19 28902444 Stein MB 2017-09-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/28902444 Genomewide association studies of suicide attempts in US soldiers. Suicide attempts 311 European ancestry cases, 83 African cases, 79 Hispanic/Latino cases, 6,228 European ancestry controls, 1,689 African controls, 1,861 Hispanic/Latino controls 89 European ancestry cases, 17 African cases, 29 Hispanic/Latino cases, 4,594 European ancestry controls, 823 African controls, 1,462 Hispanic/Latino controls Illumina [at least 360704] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST004893 Genome-wide genotyping array 2017-11-10 28991256 Li Z 2017-10-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28991256 Genome-wide association analysis identifies 30 new susceptibility loci for schizophrenia. Schizophrenia 7,699 Chinese ancestry cases, 35,476 European ancestry cases, 18,327 Chinese ancestry controls, 46,839 European ancestry controls 4,384 Chinese ancestry cases, 5,770 Chinese ancestry controls Affymetrix, Illumina [up to 5107227] (imputed) 222 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST004946 Genome-wide genotyping array 2017-10-05 28843344 Lv WQ 2017-08-23 J Mol Cell Cardiol www.ncbi.nlm.nih.gov/pubmed/28843344 Novel common variants associated with body mass index and coronary artery disease detected using a pleiotropic cFDR method. Coronary artery disease and/or body mass index (pleiotropy) 249,796 European ancestry individuals, 15,420 European and South Asian ancestry coronary artery disease cases, 15,062 European and South Asian controls 22,233 European ancestry cases, 64,762 European controls NR [NR] 0 body mass index, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0001645 GCST004838 Genome-wide genotyping array 2017-02-24 27576016 Zhao B 2016-08-30 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/27576016 A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury. Acute kidney injury in critical illness 709 European ancestry cases, 619 European ancestry controls 206 European ancestry cases, 1,406 European ancestry controls Illumina [9076120] (imputed) 3 Acute kidney injury http://purl.obolibrary.org/obo/HP_0001919 GCST003656 Genome-wide genotyping array 2017-03-16 27579533 Zhang M 2016-08-01 Oncotarget www.ncbi.nlm.nih.gov/pubmed/27579533 Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21. Pancreatic cancer 5,107 European ancestry cases, 8,845 European ancestry controls 6,076 cases, 7,555 controls Illumina [9132527] (imputed) 3 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST003758 Genome-wide genotyping array 2018-04-18 29432556 Brooke RJ 2018-02-08 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/29432556 A High-risk Haplotype for Premature Menopause in Childhood Cancer Survivors Exposed to Gonadotoxic Therapy. Premature menopause in childhood cancer survivors 27 European ancestry cases, 3 African ancestry cases, 658 European ancestry controls, 111 African ancestry controls NA Affymetrix [10993255] (imputed) 8 primary ovarian insufficiency http://www.ebi.ac.uk/efo/EFO_0004266 GCST005518 Genome-wide genotyping array 2017-11-21 29016859 Ogura Y 2017-10-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29016859 A functional variant in MIR4300HG, the host gene of microRNA MIR4300 is associated with progression of adolescent idiopathic scoliosis. Curve progression in adolescent idiopathic scoliosis 1,105 Japanese ancestry AIS progression cases, 832 Japanese ancestry AIS non-progression controls 323 Japanese ancestry AIS progression cases, 283 Japanese ancestry AIS non-progression controls Illumina [7521072] (imputed) 1 adolescent idiopathic scoliosis, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0005423, http://www.ebi.ac.uk/efo/EFO_0008336 GCST004981 Genome-wide genotyping array 2018-06-05 29563342 Li XS 2018-03-22 JCI Insight www.ncbi.nlm.nih.gov/pubmed/29563342 Untargeted metabolomics identifies trimethyllysine, a TMAO-producing nutrient precursor, as a predictor of incident cardiovascular disease risk. Plasma trimethyllysine levels 1,297 European ancestry individuals NA Affymetrix [9012028] (imputed) 6 trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0009134 GCST005670 Genome-wide genotyping array 2017-03-11 27539887 Chahal HS 2016-08-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27539887 Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma. Basal cell carcinoma 12.945 European ancestry cases, 274,252 European ancestry controls 4,242 European ancestry cases, 12,802 European ancestry controls Illumina [at least 560000] (imputed) 33 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST003726 Genome-wide genotyping array 2017-02-10 27564568 Liu C 2016-08-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/27564568 Genomewide Approach Validates Thiopurine Methyltransferase Activity Is a Monogenic Pharmacogenomic Trait. Thiopurine methyltransferase activity in acute lymphoblastic leukemia patients treated with mercaptopurines up to 407 European ancestry cases, up to 138 African ancestry cases, up to 251 Hispanic cases, up to 57 Asian ancestry cases, up to 110 other ancestry cases NA Affymetrix, Illumina [9000000] (imputed) 1 thiopurine methyltransferase activity measurement, response to mercaptopurine http://www.ebi.ac.uk/efo/EFO_0007852, http://www.ebi.ac.uk/efo/EFO_0007853 GCST003609 Genome-wide genotyping array 2017-02-19 27561104 Pirastu N 2016-08-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27561104 Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption. Coffee consumption 370 Carlantino (founder/genetic isolate) individuals, 843 Friuli Venezia Giulia (founder/genetic isolate) individuals 1,731 Erasmus Rucphen (founder/genetic isolate) individuals Illumina [at least 3692733] (imputed) 5 coffee consumption, cups of coffee per day measurement http://www.ebi.ac.uk/efo/EFO_0004330, http://www.ebi.ac.uk/efo/EFO_0006782 GCST003621 Genome-wide genotyping array 2017-03-11 27545300 Hao J 2016-08-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27545300 A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease. Joint destruction and growth retardation 90 East Asian ancestry Kashin-Beck disease cases, 1,627 East Asian ancestry controls 403 East Asian ancestry Kashin-Beck disease cases, 297 East Asian ancestry controls Affymetrix [532894] 0 Kashin-Beck disease, joint damage measurement, height growth measurement http://www.ebi.ac.uk/efo/EFO_0006511, http://www.ebi.ac.uk/efo/EFO_0005413, http://www.ebi.ac.uk/efo/EFO_0005201 GCST003727 Genome-wide genotyping array 2017-03-14 27568811 Marinelli M 2016-08-19 Sleep www.ncbi.nlm.nih.gov/pubmed/27568811 Heritability and Genome-Wide Association Analyses of Sleep Duration in Children: The EAGLE Consortium. Sleep duration 10,554 European ancestry children 1,250 European ancestry children Affymetrix, Illumina [at least 5306521] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST003741 Genome-wide genotyping array 2018-06-12 29495898 Peterson RE 2018-03-02 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/29495898 Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression. Major depressive disorder 4,785 Han Chinese ancestry cases, 4,814 Han Chinese ancestry controls NA NR [4313801] (imputed) 3 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005691 Genome-wide genotyping array 2018-06-12 29495898 Peterson RE 2018-03-02 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/29495898 Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression. Major depressive disorder (exposed to adversity) 1,646 Han Chinese ancestry cases, 982 Han Chinese ancestry controls NA NR [4313801] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005690 Genome-wide genotyping array 2018-06-12 29495898 Peterson RE 2018-03-02 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/29495898 Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression. Major depressive disorder (unexposed to adversity) 3,139 Han Chinese ancestry cases, 3,832 Han Chinese ancestry controls NA NR [4313801] (imputed) 4 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005689 Genome-wide genotyping array 2018-07-04 29538362 Jilling T 2018-03-14 Pediatr Res www.ncbi.nlm.nih.gov/pubmed/29538362 Surgical necrotizing enterocolitis in extremely premature neonates is associated with genetic variations in an intergenic region of chromosome eight. Surgical necrotising enterocolitis in extremely premature birth 20 African American cases, 6 Hispanic Caucasian cases, 4 European ancestry cases, 283 African American controls, 130 Hispanic Caucasian controls, 133 European ancestry controls, NA Illumina [8270200] (imputed) 29 necrotizing enterocolitis http://www.ebi.ac.uk/efo/EFO_0003928 GCST005800 Genome-wide genotyping array 2017-02-09 27545685 Biernacka JM 2016-08-03 Parkinsonism Relat Disord www.ncbi.nlm.nih.gov/pubmed/27545685 Genome-wide gene-environment interaction analysis of pesticide exposure and risk of Parkinson's disease. Parkinson's disease (pesticide exposure interaction) 364 cases, 364 sibling controls NA Perlegen [735843] (imputed) 1 pesticide exposure measurement, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0007840, http://purl.obolibrary.org/obo/MONDO_0005180 GCST003600 Genome-wide genotyping array 2018-02-27 29382897 Pagerols M 2018-01-30 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29382897 Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder. Response to methylphenidate treatment in attention-deficit/hyperactivity disorder 141 European ancestry responder child cases, 32 European ancestry non-responder child cases 161 Brazilian responder cases, 28 Brazilian non-responder cases Illumina [3566199] (imputed) 0 response to methylphenidate http://purl.obolibrary.org/obo/GO_0036271 GCST005318 Genome-wide genotyping array 2018-10-22 27487801 Wu S 2016-11-01 Hum Genet www.ncbi.nlm.nih.gov/pubmed/27487801 Genome-wide scans reveal variants at EDAR predominantly affecting hair straightness in Han Chinese and Uyghur populations. Straight vs curly hair 2,675 Han Chinese ancestry cases, 224 Han Chinese ancestry controls 357 Uyghur ancestry cases, 352 Uyghur ancestry controls Illumina [81706044] (imputed) 2 hair morphology http://www.ebi.ac.uk/efo/EFO_0005038 GCST006468 Genome-wide genotyping array 2018-02-14 29379196 Fadista J 2018-01-29 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29379196 Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus. Hirschsprung disease 170 Danish ancestry cases, 4717 Danish ancestry controls 416 European ancestry cases, 903 European ancestry controls Illumina [6162479] (imputed) 7 Hirschsprung disease http://purl.obolibrary.org/obo/MONDO_0018309 GCST005289 Genome-wide genotyping array 2018-02-28 29395996 van Laarhoven A 2018-01-23 Lancet Infect Dis www.ncbi.nlm.nih.gov/pubmed/29395996 Cerebral tryptophan metabolism and outcome of tuberculous meningitis: an observational cohort study. CSF tryptophan concentration in tuberculous meningitis 130 individuals NA Illumina [4751257] (imputed) 10 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST005331 Genome-wide genotyping array 2018-03-12 29398083 Lores-Motta L 2018-02-01 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/29398083 Genome-Wide Association Study Reveals Variants in CFH and CFHR4 Associated with Systemic Complement Activation: Implications in Age-Related Macular Degeneration. Serum C3d:C3 ratio (systemic complement activation) up to 1,548 European ancestry individuals up to 697 European ancestry individuals Illumina [9972920] (imputed) 2 c3d:C3 ratio http://www.ebi.ac.uk/efo/EFO_0008543 GCST005365 Genome-wide genotyping array 2017-02-10 27569725 Yang SK 2016-08-25 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/27569725 Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans. Inflammatory bowel disease 1,505 Korean ancestry cases, 4,041 Korean ancestry controls 1,989 Korean ancestry cases, 3,491 Korean ancestry controls Illumina [522285] 15 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST003602 Genome-wide genotyping array 2018-03-23 29391396 McElroy SL 2018-02-02 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29391396 Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. Binge eating behaviour in bipolar disorder 398 European ancestry bipolar disorder cases, 1,231 European ancestry bipolar disorder controls NA Affymetrix, Illumina [8000000] (imputed) 5 binge eating http://www.ebi.ac.uk/efo/EFO_0005924 GCST005387 Genome-wide genotyping array 2018-03-23 29391396 McElroy SL 2018-02-02 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29391396 Bipolar disorder with binge eating behavior: a genome-wide association study implicates PRR5-ARHGAP8. Binge eating behaviour and bipolar disorder 398 European ancestry cases, 1,811 European ancestry controls NA Affymetrix, Illumina [8000000] (imputed) 5 binge eating, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0005924, http://purl.obolibrary.org/obo/MONDO_0004985 GCST005386 Genome-wide genotyping array 2018-03-29 29391395 Strawbridge RJ 2018-02-02 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29391395 Genome-wide analysis of self-reported risk-taking behaviour and cross-disorder genetic correlations in the UK Biobank cohort. Self-reported risk-taking behaviour 29,703 British ancestry cases, 86,552 British ancestry controls 35,210 British ancestry cases, 104,263 British ancestry controls Affymetrix [8781003] (imputed) 1 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST005415 Genome-wide genotyping array 2018-03-01 29397368 Meng W 2018-01-31 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/29397368 A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773). Headache 74,461 British ancestry cases, 149,321 British ancestry controls NA Affymetrix [9304965] (imputed) 28 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST005337 Genome-wide genotyping array 2018-05-11 29436472 Casalone E 2018-02-07 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29436472 A novel variant in GLIS3 is associated with osteoarthritis. Osteoarthritis of the hip or knee (with total joint replacement) 5,414 European ancestry cases, 9,939 European ancestry healthy controls 17,894 European ancestry cases, 89,470 European ancestry healthy controls Illumina [270934] 1 osteoarthritis, hip, osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616 GCST005571 Genome-wide genotyping array 2018-05-11 29436472 Casalone E 2018-02-07 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29436472 A novel variant in GLIS3 is associated with osteoarthritis. Osteoarthritis of the hip or knee 5,414 European ancestry cases, 9,939 European ancestry healthy controls 12,658 European ancestry cases, 50,898 European ancestry healthy controls Illumina [270934] 2 osteoarthritis, hip, osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616 GCST005573 Genome-wide genotyping array 2018-05-11 29436472 Casalone E 2018-02-07 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29436472 A novel variant in GLIS3 is associated with osteoarthritis. Osteoarthritis of the hip (with total joint replacement) 2,517 European ancestry cases, 9,939 European ancestry healthy controls 2,282 European ancestry cases, 9,193 European ancestry healthy controls Illumina [270934] 6 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST005572 Genome-wide genotyping array 2018-05-11 29436472 Casalone E 2018-02-07 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29436472 A novel variant in GLIS3 is associated with osteoarthritis. Osteoarthritis of the knee (with total joint replacement) 2,188 European ancestry cases, 9,939 European ancestry healthy controls 2,281 European ancestry cases, 9,194 European ancestry healthy controls Illumina [270934] 5 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST005574 Genome-wide genotyping array 2018-09-20 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to antipsychotic treatment in schizophrenia 2,413 Han Chinese ancestry cases 1,379 Han Chinese ancestry cases Illumina [6097251] (imputed) 10 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST006292 Genome-wide genotyping array 2018-09-20 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to haloperidol in schizophrenia 192 Han Chinese ancestry cases NA Illumina [6097251] (imputed) 6 response to haloperidol http://purl.obolibrary.org/obo/GO_1905119 GCST006298 Genome-wide genotyping array 2018-09-20 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to perphenazine in schizophrenia 193 Han Chinese ancestry cases NA Illumina [6097251] (imputed) 5 response to perphenazine http://purl.obolibrary.org/obo/GO_0097334 GCST006297 Genome-wide genotyping array 2018-09-20 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to ziprazidone in schizophrenia 408 Han Chinese ancestry cases NA Illumina [6097251] (imputed) 9 response to ziprasidone http://purl.obolibrary.org/obo/GO_0097337 GCST006296 Genome-wide genotyping array 2018-09-20 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to quetiapine in schizophrenia 386 Han Chinese ancestry cases NA Illumina [6097251] (imputed) 15 response to quetiapine http://purl.obolibrary.org/obo/GO_0097335 GCST006295 Genome-wide genotyping array 2018-09-19 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to aripiprazole in schizophrenia 397 Han Chinese ancestry cases 405 Han Chinese ancestry cases Illumina [6097251] (imputed) 2 response to aripiprazole, response to antipsychotic drug http://www.ebi.ac.uk/efo/EFO_0009261, http://purl.obolibrary.org/obo/GO_0097332 GCST006285 Genome-wide genotyping array 2018-09-20 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to risperidone in schizophrenia 425 Han Chinese ancestry cases 559 Han Chinese ancestry cases Illumina [6097251] (imputed) 1 response to risperidone http://purl.obolibrary.org/obo/GO_0097336 GCST006294 Genome-wide genotyping array 2018-09-20 29503163 Yu H 2018-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/29503163 Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study. Response to olanzapine in schizophrenia 412 Han Chinese ancestry cases 415 Han Chinese ancestry cases Illumina [6097251] (imputed) 2 response to olanzapine http://purl.obolibrary.org/obo/GO_0097333 GCST006293 Genome-wide genotyping array 2018-06-29 29494758 Liu L 2018-03-01 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/29494758 Genome-wide association study identifies three novel susceptibility loci for systemic lupus erythematosus in Han Chinese. Systemic lupus erythematosus 1,047 Han Chinese ancestry cases, 1,205 Han Chinese ancestry controls 3,509 Han Chinese ancestry cases, 8,246 Han Chinese ancestry controls NR [at least 493955] (imputed) 3 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST005754 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Neurociticism 380,506 European ancestry individuals NA NR [10847151] (imputed) 181 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST006940 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Irritable mood 366,726 European ancestry individuals NA NR [~ 10847151] (imputed) 67 irritability measurement http://www.ebi.ac.uk/efo/EFO_0009594 GCST006941 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling lonely 376,352 European ancestry individuals NA NR [10847151] (imputed) 10 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST006942 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling miserable 376,097 European ancestry individuals NA NR [10847151] (imputed) 64 feeling miserable measurement http://www.ebi.ac.uk/efo/EFO_0009598 GCST006943 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Experiencing mood swings 373,733 European ancestry individuals NA NR [10847151] (imputed) 69 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST006944 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling guilty 373,380 European ancestry individuals NA NR [10847151] (imputed) 29 guilt measurement http://www.ebi.ac.uk/efo/EFO_0009595 GCST006945 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Worry too long after an embarrassing experience 367,725 European ancestry individuals NA NR [10847151] (imputed) 34 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST006946 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling fed-up 374,971 European ancestry individuals NA NR [10847151] (imputed) 60 feeling "fed-up" measurement http://www.ebi.ac.uk/efo/EFO_0009588 GCST006947 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling nervous 373,121 European ancestry individuals NA NR [10847151] (imputed) 67 feeling nervous measurement http://www.ebi.ac.uk/efo/EFO_0009597 GCST006948 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Suffering from nerves 369,499 European ancestry individuals NA NR [10847151] (imputed) 12 nervousness http://purl.obolibrary.org/obo/NCIT_C74532 GCST006949 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling worry 372,869 European ancestry individuals NA NR [10847151] (imputed) 71 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST006950 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling hurt 372,047 European ancestry individuals NA NR [10847151] (imputed) 46 feeling emotionally hurt measurement http://www.ebi.ac.uk/efo/EFO_0009599 GCST006951 Genome-wide genotyping array 2019-01-22 29500382 Nagel M 2018-03-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29500382 Item-level analyses reveal genetic heterogeneity in neuroticism. Feeling tense 371,318 European ancestry individuals NA NR [10847151] (imputed) 33 feeling tense measurement http://www.ebi.ac.uk/efo/EFO_0009596 GCST006952 Genome-wide genotyping array 2018-06-29 29496196 McCoy TH Jr. 2018-02-20 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29496196 Genome-wide Association Study of Dimensional Psychopathology Using Electronic Health Records. Dimensional psychopathology (Negative) 4,687 Northern European ancestry individuals NA Illumina [893900] (imputed) 10 negative domain measurement http://www.ebi.ac.uk/efo/EFO_0009096 GCST005756 Genome-wide genotyping array 2018-06-29 29496196 McCoy TH Jr. 2018-02-20 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29496196 Genome-wide Association Study of Dimensional Psychopathology Using Electronic Health Records. Dimensional psychopathology (Positive) 4,687 Northern European ancestry individuals NA Illumina [893900] (imputed) 10 positive domain measurement http://www.ebi.ac.uk/efo/EFO_0009097 GCST005757 Genome-wide genotyping array 2018-06-29 29496196 McCoy TH Jr. 2018-02-20 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29496196 Genome-wide Association Study of Dimensional Psychopathology Using Electronic Health Records. Dimensional psychopathology (Arousal) 4,687 Northern European ancestry individuals NA Illumina [893900] (imputed) 10 arousal domain measurement http://www.ebi.ac.uk/efo/EFO_0009099 GCST005758 Genome-wide genotyping array 2018-06-29 29496196 McCoy TH Jr. 2018-02-20 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29496196 Genome-wide Association Study of Dimensional Psychopathology Using Electronic Health Records. Dimensional psychopathology (Social) 4,687 Northern European ancestry individuals NA Illumina [893900] (imputed) 10 social domain measurement http://www.ebi.ac.uk/efo/EFO_0009100 GCST005759 Genome-wide genotyping array 2018-06-29 29496196 McCoy TH Jr. 2018-02-20 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29496196 Genome-wide Association Study of Dimensional Psychopathology Using Electronic Health Records. Dimensional psychopathology (Cognitive) 4,687 Northern European ancestry individuals NA Illumina [893900] (imputed) 10 cognitive domain measurement http://www.ebi.ac.uk/efo/EFO_0009098 GCST005760 Genome-wide genotyping array 2018-12-17 22833195 Terracciano A 2011-10-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/22833195 Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking. Excitement-seeking behaviour 4,375 Sardinian (founder/genetic isolate) individuals, 343 Cilento (founder/genetic isolate) individuals, 3,142 European ancestry individuals 2,062 European ancestry individuals, 3,043 individuals Affymetrix, Illumina [at least 2000000] (imputed) 0 personality trait measurement http://www.ebi.ac.uk/efo/EFO_0007911 GCST006796 Genome-wide genotyping array 2018-04-30 26367794 Zheng HF 2015-10-01 Nature www.ncbi.nlm.nih.gov/pubmed/26367794 Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Femoral neck bone mineral density 26,320 European ancestry individuals, 2,868 whole genome sequenced European ancestry individuals, 3,547 whole exome sequenced European ancestry individuals 17,253 European ancestry individuals Illumina [at least 10916125] (imputed) 3 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST005544 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2018-04-30 26367794 Zheng HF 2015-10-01 Nature www.ncbi.nlm.nih.gov/pubmed/26367794 Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Lumbar spine bone mineral density 23,699 European ancestry individuals, 1,526 whole genome sequenced European ancestry individuals, 3,273 whole exome sequenced European ancestry individuals 16,233 European ancestry individuals Illumina [at least 10923926] (imputed) 4 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST005545 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2018-04-30 26367794 Zheng HF 2015-10-01 Nature www.ncbi.nlm.nih.gov/pubmed/26367794 Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture. Forearm bone mineral density 6,627 European ancestry individuals, 1,221 whole genome sequenced European ancestry individuals, 295 whole exome sequenced European ancestry individuals, 2,662 European ancestry individuals Illumina [at least 14018627] (imputed) 2 radius bone mineral density http://www.ebi.ac.uk/efo/EFO_0007933 GCST005546 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2017-12-18 29066854 Lin BD 2017-11-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29066854 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. Platelet-to-lymphocyte ratio 5,901 Dutch ancestry individuals 2,538 individuals Affymetrix, Illumina, Perlegen [6010458] (imputed) 0 platelet-to-lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0008446 GCST005052 Genome-wide genotyping array 2017-12-18 29066854 Lin BD 2017-11-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29066854 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. Neutrophil count 5,901 Dutch ancestry individuals 2,538 individuals Affymetrix, Illumina, Perlegen [6010458] (imputed) 1 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST005056 Genome-wide genotyping array 2017-12-18 29066854 Lin BD 2017-11-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29066854 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. Lymphocyte count 5,901 Dutch ancestry individuals 2,538 individuals Affymetrix, Illumina, Perlegen [6010458] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST005055 Genome-wide genotyping array 2017-12-18 29066854 Lin BD 2017-11-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29066854 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. Platelet count 5,901 Dutch ancestry individuals 2,538 individuals Affymetrix, Illumina, Perlegen [6010458] (imputed) 5 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST005054 Genome-wide genotyping array 2017-12-18 29066854 Lin BD 2017-11-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29066854 2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio. Neutrophil-to-lymphocyte ratio 5,901 Dutch ancestry individuals 2,538 individuals Affymetrix, Illumina, Perlegen [6010458] (imputed) 0 neutrophil-to-lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0008447 GCST005053 Genome-wide genotyping array 2017-12-11 21908519 Huffman JE 2011-12-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21908519 Polymorphisms in B3GAT1, SLC9A9 and MGAT5 are associated with variation within the human plasma N-glycome of 3533 European adults. N-glycan levels Up to 1,426 European ancestry male individuals, up to 1,941 European ancestry female individuals NA Illumina [NR] 41 N-glycan measurement http://www.ebi.ac.uk/efo/EFO_0004999 GCST005046 Genome-wide genotyping array 2018-01-15 29170429 Hachiya T 2017-11-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29170429 Genome-wide meta-analysis in Japanese populations identifies novel variants at the TMC6-TMC8 and SIX3-SIX2 loci associated with HbA1c. Glycated hemoglobin levels 7,704 Japanese ancestry individuals NA Illumina [7135436] (imputed) 7 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST005145 Genome-wide genotyping array 2018-04-30 28714976 Sims R 2017-09-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28714976 Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Alzheimer's disease (late onset) up to 16,097 European ancestry cases, up to 18,077 European ancestry controls up to 20,693 European ancestry cases, up to 30,266 European ancestry controls Illumina [241551] 17 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST005549 Exome genotyping array 2017-12-05 29029846 Schormair B 2017-11-01 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29029846 Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis. Restless legs syndrome 15,126 European ancestry cases, 95,725 European ancestry controls 30,770 European ancestry cases, 286,913 European ancestry controls Affymetrix, Illumina [6864281] (imputed) 20 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST005042 Genome-wide genotyping array 2018-08-20 29240982 Mitchell JA 2017-12-14 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/29240982 Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton. Pediatric areal bone mineral density (concordant skeletal phenotype) 470 European ancestry females, 463 European ancestry males, 256 African and Asian ancestry females, 210 African and Asian ancestry males 238 European ancestry females, 246 European ancestry males Illumina [NR] (imputed) 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST006130 Genome-wide genotyping array 2018-09-11 29240982 Mitchell JA 2017-12-14 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/29240982 Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton. Pediatric areal bone mineral density (radius vs spine & hip discordant skeletal phenotype) 470 European ancestry females, 463 European ancestry males, 256 African and Asian ancestry females, 210 African and Asian ancestry males 238 European ancestry females, 246 European ancestry males Illumina [NR] (imputed) 4 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST006247 Genome-wide genotyping array 2018-08-20 29240982 Mitchell JA 2017-12-14 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/29240982 Multi-dimensional bone density phenotyping reveals new insights in to genetic regulation of the pediatric skeleton. Pediatric areal bone mineral density (spine vs radius & hip discordant skeletal phenotype) 470 European ancestry females, 463 European ancestry males, 256 African and Asian ancestry females, 210 African and Asian ancestry males 238 European ancestry females, 246 European ancestry males Illumina [NR] (imputed) 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST006129 Genome-wide genotyping array 2017-09-27 28783044 Ware JS 2017-08-07 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28783044 Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremia. Thiazide-induced hyponatremia 48 European ancestry cases, 2,905 European ancestry controls 94 European ancestry cases, 106 European ancestry controls Illumina [502663] 0 thiazide-induced hyponatremia http://www.ebi.ac.uk/efo/EFO_0008349 GCST004786 Genome-wide genotyping array 2017-11-17 29018042 Schierding W 2017-10-10 J Med Genet www.ncbi.nlm.nih.gov/pubmed/29018042 GWAS on prolonged gestation (post-term birth): analysis of successive Finnish birth cohorts. Post-term birth 1,167 European ancestry post-term-born individuals, 3,625 European ancestry term-born individuals NA Illumina [at least 3855963] (imputed) 0 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST004951 Genome-wide genotyping array 2018-06-21 27362418 Zhang H 2016-06-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27362418 A Powerful Procedure for Pathway-Based Meta-analysis Using Summary Statistics Identifies 43 Pathways Associated with Type II Diabetes in European Populations. Type 2 diabetes 19,809 European ancestry cases, 111,181 European ancestry controls 6,952 East Asian ancestry cases, 11,865 East Asian ancestry controls NR [up to 2500000] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST005716 Genome-wide genotyping array 2018-01-30 29288229 McCormack M 2017-12-29 Neurology www.ncbi.nlm.nih.gov/pubmed/29288229 Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Antiepileptic drug-induced maculopapular exanthema 259 European ancestry cases, 979 European ancestry tolerant controls, 116 Han Chinese ancestry cases, 342 Han Chinese ancestry tolerant controls NA Illumina [at least 3693290] (imputed) 0 maculopapular eruption, response to anticonvulsant http://www.ebi.ac.uk/efo/EFO_1001253, http://purl.obolibrary.org/obo/GO_0036277 GCST005197 Genome-wide genotyping array 2018-01-30 29288229 McCormack M 2017-12-29 Neurology www.ncbi.nlm.nih.gov/pubmed/29288229 Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Carbamazepine-induced maculopapular exanthema 95 European ancestry cases, 869 European ancestry tolerant controls, 85 Han Chinese ancestry cases, 197 Han Chinese ancestry tolerant controls NA Illumina [at least 3693290] (imputed) 1 maculopapular eruption, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_1001253, http://www.ebi.ac.uk/efo/EFO_0008484 GCST005198 Genome-wide genotyping array 2018-01-30 29288229 McCormack M 2017-12-29 Neurology www.ncbi.nlm.nih.gov/pubmed/29288229 Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Lamotrigine-induced maculopapular exanthema 118 European ancestry cases, 812 European ancestry tolerant controls, 16 Han Chinese ancestry cases, 32 Han Chinese ancestry tolerant controls NA Illumina [at least 3693290] (imputed) 0 response to lamotrigine, maculopapular eruption http://www.ebi.ac.uk/efo/EFO_0007661, http://www.ebi.ac.uk/efo/EFO_1001253 GCST005199 Genome-wide genotyping array 2018-01-30 29288229 McCormack M 2017-12-29 Neurology www.ncbi.nlm.nih.gov/pubmed/29288229 Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients. Phenytoin-induced maculopapular exanthema 52 European ancestry cases, 472 European ancestry tolerant controls, 22 Han Chinese ancestry cases, 58 Han Chinese ancestry tolerant controls 13 European ancestry cases, 88 European ancestry tolerant controls Illumina [at least 3693290] (imputed) 1 maculopapular eruption, response to phenytoin http://www.ebi.ac.uk/efo/EFO_1001253, http://www.ebi.ac.uk/efo/EFO_0006345 GCST005200 Genome-wide genotyping array 2018-02-19 29290336 Nielsen JB 2018-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29290336 Genome-wide Study of Atrial Fibrillation Identifies Seven Risk Loci and Highlights Biological Pathways and Regulatory Elements Involved in Cardiac Development. Atrial fibrillation 6,337 European ancestry cases, 61,607 European ancestry controls 30,679 European ancestry cases, 278,895 European ancestry controls Illumina [8952551] (imputed) 10 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST005306 Genome-wide genotyping array 2018-07-12 29773799 Horikoshi M 2018-05-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29773799 Elucidating the genetic architecture of reproductive ageing in the Japanese population. Menopause (age at onset) 43,861 Japanese ancestry women 32,545 European ancestry women Illumina [at least 532488] (imputed) 36 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST005863 Genome-wide genotyping array 2018-07-12 29773799 Horikoshi M 2018-05-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29773799 Elucidating the genetic architecture of reproductive ageing in the Japanese population. Menarche (age at onset) 67,029 Japanese ancestry women 73,397 European ancestry women Illumina [at least 532488] (imputed) 31 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST005867 Genome-wide genotyping array 2018-07-12 29773799 Horikoshi M 2018-05-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29773799 Elucidating the genetic architecture of reproductive ageing in the Japanese population. Early age at menarche 15,709 Japanese ancestry early age at menarche individuals, 14,557 Japanese ancestry median age at menarche individuals NA Illumina [at least 532488] (imputed) 1 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST005865 Genome-wide genotyping array 2018-07-12 29773799 Horikoshi M 2018-05-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29773799 Elucidating the genetic architecture of reproductive ageing in the Japanese population. Late age at menarche 10,875 Japanese ancestry late age at menarche individuals, 14,557 Japanese ancestry median age at menarche individuals NA Illumina [at least 532488] (imputed) 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST005864 Genome-wide genotyping array 2018-03-08 29293525 Gudmundsdottir V 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293525 Integrative network analysis highlights biological processes underlying GLP-1 stimulated insulin secretion: A DIRECT study. GLP-1-stimulated insulin secretion 33 monozygotic twin pairs, 14 dizygotic twin pairs, 32 individuals 100 European ancestry individuals Illumina [6600000] (imputed) 0 GLP-1-stimulated insulin response http://www.ebi.ac.uk/efo/EFO_0008531 GCST005353 Genome-wide genotyping array 2017-09-22 28809852 Liu L 2017-08-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/28809852 The SNP-set based association study identifies ITGA1 as a susceptibility gene of attention-deficit/hyperactivity disorder in Han Chinese. Attention deficit hyperactivity disorder 1,033 Han Chinese ancestry cases, 950 Han Chinese ancestry controls 1,441 Han Chinese ancestry cases, 1,447 Han Chinese ancestry controls Affymetrix [717417] 1 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST004778 Genome-wide genotyping array 2018-06-19 29521573 Buck D 2018-03-01 Mult Scler www.ncbi.nlm.nih.gov/pubmed/29521573 Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. Neutralising antibody response to interferon beta therapy in multiple sclerosis (time to production) 361 European, Hispanic, Asian, African or unknown ancestry cases NA Affymetrix [8671751] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST005710 Genome-wide genotyping array 2018-06-19 29521573 Buck D 2018-03-01 Mult Scler www.ncbi.nlm.nih.gov/pubmed/29521573 Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies) 361 European, Hispanic, Asian, African or unknown ancestry cases, 580 European, Hispanic, Asian, African or unknown ancestry controls NA Affymetrix [8671751] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST005706 Genome-wide genotyping array 2018-06-19 29521573 Buck D 2018-03-01 Mult Scler www.ncbi.nlm.nih.gov/pubmed/29521573 Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. Neutralising antibody response to interferon beta therapy in multiple sclerosis (mean antibody levels) 926 European ancestry individuals, 7 Hispanic individuals, 1 Asian ancestry individuals, 1 African ancestry individual, 4 other unknown ancestry individuals, 2 individuals NA Affymetrix [8671751] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST005707 Genome-wide genotyping array 2018-06-19 29521573 Buck D 2018-03-01 Mult Scler www.ncbi.nlm.nih.gov/pubmed/29521573 Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. Neutralising antibody response to interferon beta therapy in multiple sclerosis (area under the curve for the first two years) 926 European ancestry individuals, 7 Hispanic individuals, 1 Asian ancestry individuals, 1 African ancestry individual, 4 other unknown ancestry individuals, 2 individuals NA Affymetrix [8671751] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST005708 Genome-wide genotyping array 2018-06-19 29521573 Buck D 2018-03-01 Mult Scler www.ncbi.nlm.nih.gov/pubmed/29521573 Effect of HLA-DRB1 alleles and genetic variants on the development of neutralizing antibodies to interferon beta in the BEYOND and BENEFIT trials. Neutralising antibody response to interferon beta therapy in multiple sclerosis (maximum antibody levels) 926 European ancestry individuals, 7 Hispanic individuals, 1 Asian ancestry individuals, 1 African ancestry individual, 4 other unknown ancestry individuals, 2 individuals NA Affymetrix [8671751] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST005709 Genome-wide genotyping array 2018-07-30 27618447 Surendran P 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618447 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Diastolic blood pressure up to 165,276 European ancestry individuals, up to 27,487 South Asian ancestry individuals up to 125,713 European ancestry individuals, up to 2,641 South Asian ancestry individuals, 4,632 Hispanic individuals, 22,077 African American individuals Illumina [242296] 44 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST006020 Targeted genotyping array [Exome array] 2018-07-30 27618447 Surendran P 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618447 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Systolic blood pressure up to 165,276 European ancestry individuals, up to 27,487 South Asian ancestry individuals up to 125,713 European ancestry individuals, up to 2,641 South Asian ancestry individuals, 4,632 Hispanic individuals, 22,077 African American individuals Illumina [242296] 45 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST006021 Targeted genotyping array [Exome array] 2018-07-30 27618447 Surendran P 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618447 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Pulse pressure up to 165,276 European ancestry individuals, up to 27,487 South Asian ancestry individuals up to 125,713 European ancestry individuals, up to 2,641 South Asian ancestry individuals, 4,632 Hispanic individuals, 22,077 African American individuals Illumina [242296] 17 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST006022 Targeted genotyping array [Exome array] 2018-07-30 27618447 Surendran P 2016-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618447 Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension. Hypertension up to 83,330 European ancestry cases, up to 73,760 European ancestry controls, up to 9,322 South Asian ancestry cases, up to 16,861 South Asian ancestry controls up to 125,713 European ancestry individuals, up to 2,641 South Asian ancestry individuals, 4,632 Hispanic individuals, 22,077 African American individuals Illumina [242296] 12 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST006023 Targeted genotyping array [Exome array] 2018-07-04 29422769 Shah RL 2018-02-05 Mol Vis www.ncbi.nlm.nih.gov/pubmed/29422769 A genome-wide association study of corneal astigmatism: The CREAM Consortium. Corneal astigmatism 9,293 European ancestry cases, 12,957 European ancestry controls, 4,349 Asian ancestry cases, 4,771 Asian ancestry controls NA NR [~ 55000000] (imputed) 16 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST005803 Genome-wide genotyping array 2018-04-06 29404672 Roshandel D 2018-02-05 Diabetologia www.ncbi.nlm.nih.gov/pubmed/29404672 Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes. Stimulated C-peptide levels in type I diabetes 1,303 European ancestry individuals NA Illumina [8978838] (imputed) 2 C-peptide measurement http://www.ebi.ac.uk/efo/EFO_0005187 GCST005435 Genome-wide genotyping array 2018-04-06 29404672 Roshandel D 2018-02-05 Diabetologia www.ncbi.nlm.nih.gov/pubmed/29404672 Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes. Fasting C-peptide levels in type I diabetes 2,019 European ancestry individuals NA Illumina [8375292] (imputed) 0 C-peptide measurement http://www.ebi.ac.uk/efo/EFO_0005187 GCST005438 Genome-wide genotyping array 2018-04-06 29404672 Roshandel D 2018-02-05 Diabetologia www.ncbi.nlm.nih.gov/pubmed/29404672 Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes. Random C-peptide levels in type I diabetes 1,497 European ancestry individuals NA Illumina [8320327] (imputed) 1 C-peptide measurement http://www.ebi.ac.uk/efo/EFO_0005187 GCST005437 Genome-wide genotyping array 2018-04-06 29404672 Roshandel D 2018-02-05 Diabetologia www.ncbi.nlm.nih.gov/pubmed/29404672 Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes. C-peptide levels in type I diabetes 3,479 European ancestry individuals NA Illumina [7988630] (imputed) 4 C-peptide measurement http://www.ebi.ac.uk/efo/EFO_0005187 GCST005436 Genome-wide genotyping array 2018-05-11 29273593 Duan L 2017-12-22 Stroke www.ncbi.nlm.nih.gov/pubmed/29273593 Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study. Moyamoya disease 755 Han Chinese ancestry cases, 2,031 Han Chinese ancestry controls 724 Han Chinese ancestry cases, 3,043 Han Chinese ancestry controls Illumina [747089] 35 Moyamoya disease http://purl.obolibrary.org/obo/MONDO_0016820 GCST005575 Genome-wide genotyping array 2018-08-03 29030101 Asai Y 2017-10-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/29030101 Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy. Peanut allergy 1,068 European ancestry cases, 3,327 European ancestry controls, 514 cases, 2,119 controls NA Illumina [7830195] (imputed) 8 peanut allergy measurement http://www.ebi.ac.uk/efo/EFO_0007017 GCST006039 Targeted genotyping array 2018-08-03 29030101 Asai Y 2017-10-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/29030101 Genome-wide association study and meta-analysis in multiple populations identifies new loci for peanut allergy and establishes C11orf30/EMSY as a genetic risk factor for food allergy. Food allergy 1,170 European ancestry cases, 3,336 European ancestry controls, up to 6,098 cases, up to 25,748 controls NA Illumina [7830195] (imputed) 6 food allergy measurement http://www.ebi.ac.uk/efo/EFO_0007016 GCST006038 Targeted genotyping array 2018-01-26 29271184 Chung GE 2017-12-26 Gut Liver www.ncbi.nlm.nih.gov/pubmed/29271184 Genetic Polymorphisms of PNPLA3 and SAMM50 Are Associated with Nonalcoholic Fatty Liver Disease in a Korean Population. Nonalcoholic fatty liver disease 1,593 East Asian ancestry cases, 2,816 East Asian ancestry controls 744 East Asian ancestry cases, 1,137 East Asian ancestry controls Affymetrix [584061] 2 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST005190 Genome-wide genotyping array 2018-02-02 29251981 Weafer J 2017-12-01 Exp Clin Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/29251981 Hierarchical investigation of genetic influences on response inhibition in healthy young adults. Inhibitory control 934 European ancestry individuals NA Illumina [4873750] (imputed) 9 behavioural inhibitory control measurement http://www.ebi.ac.uk/efo/EFO_0008467 GCST005246 Genome-wide genotyping array 2018-02-06 29253858 Bohman A 2017-12-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29253858 A family-based genome-wide association study of chronic rhinosinusitis with nasal polyps implicates several genes in the disease pathogenesis. Chronic rhinosinusitis with nasal polyps 406 European ancestry cases, 376 European ancestry controls (first degree relatives) NA Illumina [233409] 2 chronic rhinosinusitis with nasal polyps http://www.ebi.ac.uk/efo/EFO_1002029 GCST005268 Genome-wide genotyping array 2018-01-11 29229094 Condreay L 2017-10-26 Respir Med www.ncbi.nlm.nih.gov/pubmed/29229094 No genetic association detected with mepolizumab efficacy in severe asthma. Response to mepolizumab in severe asthma 820 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 response to mepolizumab http://www.ebi.ac.uk/efo/EFO_0008459 GCST005115 Genome-wide genotyping array 2018-01-30 29273806 Demenais F 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273806 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Asthma 19,954 European ancestry cases, 107,715 European ancestry controls, 2,149 African ancestry cases, 6,055 African ancestry controls, 1,239 Japanese ancestry cases, 3,976 Japanese ancestry controls, 606 Latino cases, 792 Latino controls NA Affymetrix, Illumina, Perlegen [2831075] (imputed) 40 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST005212 Genome-wide genotyping array 2018-01-30 29273806 Demenais F 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273806 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Asthma (childhood onset) 7,131 European ancestry cases, 13,631 European ancestry controls, 1,239 Japanese ancestry cases, 3,976 Japanese ancestry controls, 606 Latino cases, 792 Latino controls NA Affymetrix, Illumina, Perlegen [2831075] (imputed) 5 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST005213 Genome-wide genotyping array 2019-01-09 29273806 Demenais F 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273806 Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. Asthma 19,954 European ancestry cases, 107,715 European ancestry controls NA Affymetrix, Illumina, Perlegen [2831075] (imputed) 24 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST006862 Genome-wide genotyping array 2017-09-05 28781888 Mobuchon L 2017-03-10 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/28781888 A GWAS in uveal melanoma identifies risk polymorphisms in the CLPTM1L locus. Uveal melanoma 259 European ancestry cases, 401 European ancestry controls 276 French cases, 184 European ancestry controls Illumina [866782] 2 Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000616 GCST004661 Genome-wide genotyping array 2017-09-29 28775256 Kawashima-Kumagai K 2017-08-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28775256 A genome-wide association study identified a novel genetic loci STON1-GTF2A1L/LHCGR/FSHR for bilaterality of neovascular age-related macular degeneration. Laterality in neovascular age-related macular degeneration 803 Japanese ancestry unilateral cases, 321 Japanese ancestry bilateral cases 132 Japanese ancestry unilateral cases, 36 Japanese ancestry bilateral cases, 78 Asian ancestry unilateral cases, 24 Asian ancestry bilateral cases Illumina [581252] 3 laterality measurement http://www.ebi.ac.uk/efo/EFO_0008372 GCST004813 Genome-wide genotyping array 2018-02-02 29230059 Sanchez-Roige S 2017-12-11 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/29230059 Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry. Delayed reward discounting 23,127 European ancestry individuals 928 European ancestry individuals Illumina [11508756] (imputed) 1 delayed reward discounting measurement http://www.ebi.ac.uk/efo/EFO_0008476 GCST005248 Genome-wide genotyping array 2018-07-04 29769521 Ramirez J 2018-05-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29769521 Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system. Heart rate response to exercise up to 35,455 European ancestry females, up to 31,802 European ancestry males NA Affymetrix [~ 7800000] (imputed) 32 heart rate response to exercise http://www.ebi.ac.uk/efo/EFO_0009184 GCST005787 Genome-wide genotyping array 2018-07-04 29769521 Ramirez J 2018-05-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29769521 Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system. Heart rate response to recovery post exercise up to 35,455 European ancestry females, up to 31,802 European ancestry males NA Affymetrix [~ 7800000] (imputed) 29 heart rate response to recovery post exercise http://www.ebi.ac.uk/efo/EFO_0009185 GCST005788 Genome-wide genotyping array 2018-07-04 29769521 Ramirez J 2018-05-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29769521 Thirty loci identified for heart rate response to exercise and recovery implicate autonomic nervous system. Resting heart rate 67,062 European ancestry individuals NA Affymetrix [~ 7800000] (imputed) 30 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST005789 Genome-wide genotyping array 2018-08-30 29505938 Dunn EC 2017-12-16 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/29505938 Genome-wide association study of depressive symptoms in the Hispanic Community Health Study/Study of Latinos. Depressive symptoms 12,310 Hispanic individuals 8,048 Hispanic individuals Illumina [2232944] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST006174 Genome-wide genotyping array 2017-10-03 28806749 Leo PJ 2017-08-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28806749 Defining the genetic susceptibility to cervical neoplasia-A genome-wide association study. Cervical cancer 2,866 European ancestry cases, 6,481 European ancestry controls NA Illumina [10863230] (imputed) 14 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST004833 Genome-wide genotyping array 2017-09-22 28762467 Wadelius M 2017-08-01 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/28762467 Sulfasalazine-Induced Agranulocytosis Is Associated With the Human Leukocyte Antigen Locus. Sulfasalazine-induced agranulocytosis 36 European ancestry cases, 5,170 European ancestry untreated controls NA Illumina [9380034] (imputed) 32 response to sulfasalazine, Drug-induced agranulocytosis http://www.ebi.ac.uk/efo/EFO_0008324, http://purl.obolibrary.org/obo/HP_0012235 GCST004781 Genome-wide genotyping array 2017-09-15 28757204 Manousaki D 2017-07-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28757204 Low-Frequency Synonymous Coding Variation in CYP2R1 Has Large Effects on Vitamin D Levels and Risk of Multiple Sclerosis. Vitamin D levels 2,619 whole genome sequenced European ancestry individuals, up to 38,213 European ancestry individuals, 1,442 individuals NA Affymetrix, Illumina [11026511] (imputed) 16 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST004726 Genome-wide genotyping array 2017-09-29 28776340 Son CN 2017-09-01 J Korean Med Sci www.ncbi.nlm.nih.gov/pubmed/28776340 ABCG2 Polymorphism Is Associated with Hyperuricemia in a Study of a Community-Based Korean Cohort. Hyperuricemia 234 Korean ancestry cases, 3,413 Korean ancestry controls NA Illumina [748585] 2 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST004825 Genome-wide genotyping array 2018-02-28 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Systemic sclerosis 1,833 European ancestry cases, 3,466 European ancestry controls, 291 African American cases, 260 African American controls NA Illumina [~ 2500000] (imputed) 6 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST005336 Genome-wide genotyping array 2018-02-28 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Limited cutaneous systemic scleroderma 1,087 European ancestry cases, 3,466 European ancestry controls, 82 African American cases, 260 African American controls NA Illumina [~ 2500000] (imputed) 6 limited scleroderma http://www.ebi.ac.uk/efo/EFO_1001017 GCST005334 Genome-wide genotyping array 2018-02-28 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Diffuse cutaneous systemic sclerosis 574 European ancestry cases, 3,466 European ancestry controls, 201 African American cases, 260 African American controls NA Illumina [~ 2500000] (imputed) 3 diffuse scleroderma http://www.ebi.ac.uk/efo/EFO_0000404 GCST005335 Genome-wide genotyping array 2018-02-28 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Systemic sclerosis (anti-centromere-positive) 671 European ancestry cases, 3,466 European ancestry controls, 21 African American cases, 260 African American controls NA Illumina [~ 2500000] (imputed) 2 anti-centromere-antibody-positive systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0008536 GCST005333 Genome-wide genotyping array 2018-02-28 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Systemic sclerosis (anti-topoisomerase-positive) 347 European ancestry cases, 3,466 European ancestry controls, 69 African American cases, 260 African American controls NA Illumina [~ 2500000] (imputed) 2 anti-topoisomerase-I-antibody-positive systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0008537 GCST005332 Genome-wide genotyping array 2018-04-30 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Systemic sclerosis 1,833 European ancestry cases, 3,466 European ancestry controls, 291 African American cases, 260 African American controls NA Illumina [126270] 10 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST005554 Targeted genotyping array [Immunochip] 2018-04-30 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Limited cutaneous systemic scleroderma 1,087 European ancestry cases, 3,466 European ancestry controls, 82 African American cases, 260 African American controls NA Illumina [126270] 8 limited scleroderma http://www.ebi.ac.uk/efo/EFO_1001017 GCST005555 Targeted genotyping array [Immunochip] 2018-04-30 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Diffuse cutaneous systemic sclerosis 574 European ancestry cases, 3,466 European ancestry controls, 201 African American cases, 260 African American controls NA Illumina [126270] 3 diffuse scleroderma http://www.ebi.ac.uk/efo/EFO_0000404 GCST005553 Targeted genotyping array [Immunochip] 2018-04-30 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Systemic sclerosis (anti-centromere-positive) 671 European ancestry cases, 3,466 European ancestry controls, 21 African American cases, 260 African American controls NA Illumina [126270] 3 anti-centromere-antibody-positive systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0008536 GCST005552 Targeted genotyping array [Immunochip] 2018-04-30 29293537 Gorlova OY 2018-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/29293537 Gene-level association analysis of systemic sclerosis: A comparison of African-Americans and White populations. Systemic sclerosis (anti-topoisomerase-positive) 347 European ancestry cases, 3,466 European ancestry controls, 69 African American cases, 260 African American controls NA Illumina [126270] 4 anti-topoisomerase-I-antibody-positive systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0008537 GCST005551 Targeted genotyping array [Immunochip] 2018-02-07 29299148 Liu W 2017-11-25 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29299148 Cancer risk susceptibility loci in a Swedish population. Cancer 3,555 Swedish ancestry cases, 15,581 Swedish ancestry controls NA Illumina [226883] 26 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST005275 Genome-wide genotyping array 2018-03-05 29278698 Zagajewska K 2017-12-23 Exp Eye Res www.ncbi.nlm.nih.gov/pubmed/29278698 GWAS links variants in neuronal development and actin remodeling related loci with pseudoexfoliation syndrome without glaucoma. Pseudoexfoliation syndrome 103 European ancestry cases, 106 European ancestry controls NA Illumina [NR] 1 exfoliation syndrome http://www.ebi.ac.uk/efo/EFO_0004235 GCST005347 Genome-wide genotyping array 2018-07-23 29296746 Ma Q 2017-06-19 Blood Adv www.ncbi.nlm.nih.gov/pubmed/29296746 Genetic variants in ADAMTS13 as well as smoking are major determinants of plasma ADAMTS13 levels. ADAMTS13 levels 3,238 European ancestry individuals NA Illumina [5821939] (imputed) 4 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST005945 Genome-wide genotyping array 2018-03-05 29304378 Medina-Gomez C 2018-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29304378 Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. Total body bone mineral density 56,284 European ancestry individuals, up to 1,333 African American individuals, up to 9,328 admixed individuals NA Affymetrix, Illumina [~ 23700000] (imputed) 242 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST005348 Genome-wide genotyping array 2018-03-05 29304378 Medina-Gomez C 2018-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29304378 Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. Total body bone mineral density (age 0-15) 11,807 European and unknown ancestry individuals NA Affymetrix, Illumina [~ 23700000] (imputed) 8 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST005345 Genome-wide genotyping array 2018-03-05 29304378 Medina-Gomez C 2018-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29304378 Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. Total body bone mineral density (age 15-30) 4,180 European and unknown ancestry individuals NA Affymetrix, Illumina [~ 23700000] (imputed) 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST005344 Genome-wide genotyping array 2018-03-05 29304378 Medina-Gomez C 2018-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29304378 Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. Total body bone mineral density (age 30-45) 10,062 European and unknown ancestry individuals NA Affymetrix, Illumina [~ 23700000] (imputed) 8 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST005346 Genome-wide genotyping array 2018-03-05 29304378 Medina-Gomez C 2018-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29304378 Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. Total body bone mineral density (age 45-60) 18,805 European individuals NA Affymetrix, Illumina [~ 23700000] (imputed) 18 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST005350 Genome-wide genotyping array 2018-03-05 29304378 Medina-Gomez C 2018-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29304378 Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects. Total body bone mineral density (age over 60) 22,504 European ancestry and African American individuals NA Affymetrix, Illumina [~ 23700000] (imputed) 20 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST005349 Genome-wide genotyping array 2018-07-20 29777097 Marioni RE 2018-05-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29777097 GWAS on family history of Alzheimer's disease. Paternal history of Alzheimer's disease 14,338 British ancestry cases, 245,941 British ancestry controls NA Affymetrix [7795605] (imputed) 2 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST005920 Genome-wide genotyping array 2018-07-20 29777097 Marioni RE 2018-05-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29777097 GWAS on family history of Alzheimer's disease. Family history of Alzheimer's disease up to 42,034 British ancestry individuals with parental history of Alzheimer's disease, at least 272,244 European ancestry individuals with no parental history of Alzheimer's disease NA Affymetrix [7795605] (imputed) 61 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST005921 Genome-wide genotyping array 2018-07-20 29777097 Marioni RE 2018-05-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29777097 GWAS on family history of Alzheimer's disease. Alzheimer's disease or family history of Alzheimer's disease up to 42,034 British ancestry individuals with parental history of Alzheimer's disease, at least 272,244 British ancestry individuals with no parental history of Alzheimer's disease, 25,580 Alzheimer's disease cases, 48,466 controls NA Affymetrix [7795605] (imputed) 221 Alzheimer disease, family history of Alzheimer’s disease http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0009268 GCST005922 Genome-wide genotyping array 2018-07-20 29777097 Marioni RE 2018-05-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/29777097 GWAS on family history of Alzheimer's disease. Maternal history of Alzheimer's disease 27,696 British ancestry cases, 260,980 British ancestry controls NA Affymetrix [7795605] (imputed) 6 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST005923 Genome-wide genotyping array 2018-05-11 29246937 Li Y 2018-02-15 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/29246937 Genome-Wide Association Study Identifies a New Locus at 7q21.13 Associated with Hepatitis B Virus-Related Hepatocellular Carcinoma. Hepatitis B virus-related hepatocellular carcinoma 348 Chinese ancestry carrier cases, 359 Chinese ancestry carrier controls, 189 Chinese ancestry trios 3,796 Chinese ancestry carrier cases, 2,544 Chinese ancestry carrier controls Affymetrix, Illumina [up to 6089459] (imputed) 2 hepatitis B virus infection, hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0004197, http://www.ebi.ac.uk/efo/EFO_0000182 GCST005570 Genome-wide genotyping array 2017-10-20 28960316 Tanskanen T 2017-09-28 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/28960316 Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci. Colorectal cancer 1,701 Finnish ancestry cases, 14,082 Finnish ancestry controls 11,647 European ancestry cases, 12,356 European ancestry controls Illumina [9068015] (imputed) 5 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST004895 Genome-wide genotyping array 2017-09-22 28836065 Hellwege JN 2017-08-23 Hum Genet www.ncbi.nlm.nih.gov/pubmed/28836065 A multi-stage genome-wide association study of uterine fibroids in African Americans. Uterine fibroids 3,999 African American cases, 4,764 African American controls NA Affymetrix, Illumina [17963051] (imputed) 4 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST004779 Genome-wide genotyping array 2018-07-17 29423119 Khan S 2017-11-28 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29423119 Meta-analysis of three genome-wide association studies identifies two loci that predict survival and treatment outcome in breast cancer. Survival in breast cancer (estrogen-receptor positive) 2,971 European ancestry individuals, 165 individuals NA Illumina [275827] (imputed) 2 event free survival time, estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000482, http://www.ebi.ac.uk/efo/EFO_1000649 GCST005901 Genome-wide genotyping array 2018-07-17 29423119 Khan S 2017-11-28 Oncotarget www.ncbi.nlm.nih.gov/pubmed/29423119 Meta-analysis of three genome-wide association studies identifies two loci that predict survival and treatment outcome in breast cancer. Survival in endocrine treated breast cancer (estrogen-receptor positive) 2,629 European ancestry individuals, 122 individuals NA Illumina [275827] (imputed) 1 event free survival time, estrogen-receptor positive breast cancer, response to endocrine therapy http://www.ebi.ac.uk/efo/EFO_0000482, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0007613 GCST005900 Genome-wide genotyping array 2017-09-22 28843169 Neumann A 2017-08-12 Psychoneuroendocrinology www.ncbi.nlm.nih.gov/pubmed/28843169 The low single nucleotide polymorphism heritability of plasma and saliva cortisol levels. Cortisol levels (saliva) 7,703 European ancestry individuals NA Illumina, Perlegen [2156702] (imputed) 10 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST004780 Genome-wide genotyping array 2017-09-25 28839172 Mahlman M 2017-08-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28839172 Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene. Bronchopulmonary dysplasia in preterm infants 60 Finnish ancestry cases, 114 Finnish ancestry controls 234 European ancestry cases, 25 African ancestry cases, 633 European ancestry controls, 51 African ancestry controls Illumina [276306] (imputed) 0 bronchopulmonary dysplasia http://purl.obolibrary.org/obo/MONDO_0019091 GCST004783 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Calcium levels 71,701 Japanese ancestry individuals NA Illumina [6108953] (imputed) 17 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST005982 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Phosphorus levels 42,793 Japanese ancestry individuals NA Illumina [6108953] (imputed) 10 phosphorus measurement http://www.ebi.ac.uk/efo/EFO_0004861 GCST005981 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Total bilirubin levels 110,207 Japanese ancestry individuals NA Illumina [6108953] (imputed) 20 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST005980 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Systolic blood pressure 136,597 Japanese ancestry individuals NA Illumina [6108953] (imputed) 23 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST005979 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Diastolic blood pressure 136,615 Japanese ancestry individuals NA Illumina [6108953] (imputed) 18 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST005978 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Mean arterial pressure 136,482 Japanese ancestry individuals NA Illumina [6108953] (imputed) 32 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST006010 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Pulse pressure 136,249 Japanese ancestry individuals NA Illumina [6108953] (imputed) 17 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST006009 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Left ventricular internal dimension in diastole 19,676 Japanese ancestry individuals NA Illumina [6108953] (imputed) 3 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST006008 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Left ventricular internal dimension in systole 19,586 Japanese ancestry individuals NA Illumina [6108953] (imputed) 4 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST006007 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Relative wall thickness 19,311 Japanese ancestry individuals NA Illumina [6108953] (imputed) 1 heart relative wall thickness http://www.ebi.ac.uk/efo/EFO_0009286 GCST006033 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Fractional shortening 19,580 Japanese ancestry individuals NA Illumina [6108953] (imputed) 4 fractional shortening http://www.ebi.ac.uk/efo/EFO_0009285 GCST006029 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Ejection fraction 19,516 Japanese ancestry individuals NA Illumina [6108953] (imputed) 3 ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0005527 GCST006006 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Interventricular septum thickness 19,318 Japanese ancestry individuals NA Illumina [6108953] (imputed) 0 interventricular septum thickness http://www.ebi.ac.uk/efo/EFO_0009287 GCST006028 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Posterior wall thickness 19,373 Japanese ancestry individuals NA Illumina [6108953] (imputed) 0 posterior wall thickness http://www.ebi.ac.uk/efo/EFO_0009288 GCST006027 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Left ventricular mass 19,076 Japanese ancestry individuals NA Illumina [6108953] (imputed) 0 left ventricular mass http://www.ebi.ac.uk/efo/EFO_0009289 GCST006026 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Left ventricular mass index 17,837 Japanese ancestry individuals NA Illumina [6108953] (imputed) 0 left ventricular mass index http://www.ebi.ac.uk/efo/EFO_0009290 GCST006025 Genome-wide genotyping array 2018-07-30 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. E/A ratio 8,600 Japanese ancestry individuals NA Illumina [6108953] (imputed) 0 E/A ratio http://www.ebi.ac.uk/efo/EFO_0009291 GCST006024 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. High density lipoprotein cholesterol levels 70,657 Japanese ancestry individuals NA Illumina [6108953] (imputed) 53 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST006005 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Low density lipoprotein cholesterol levels 72,866 Japanese ancestry individuals NA Illumina [6108953] (imputed) 29 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST006004 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Triglyceride levels 105,597 Japanese ancestry individuals NA Illumina [6108953] (imputed) 36 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST006003 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Blood sugar levels 93,146 Japanese ancestry individuals NA Illumina [6108953] (imputed) 21 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST006002 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Hemoglobin A1c levels 42,790 Japanese ancestry individuals NA Illumina [6108953] (imputed) 28 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST006001 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Immunoglobulin measurement (zinc sulfate turbidity test) 12,303 Japanese ancestry individuals NA Illumina [6108953] (imputed) 4 serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0004565 GCST006000 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Aspartate aminotransferase levels 134,154 Japanese ancestry individuals NA Illumina [6108953] (imputed) 30 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST005999 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Alanine transaminase levels 134,182 Japanese ancestry individuals NA Illumina [6108953] (imputed) 27 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST005998 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Serum alkaline phosphatase levels 105,030 Japanese ancestry individuals NA Illumina [6108953] (imputed) 48 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST006016 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Gamma glutamyl transferase levels 118,309 Japanese ancestry individuals NA Illumina [6108953] (imputed) 50 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST006019 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Activated partial thromboplastin time 37,767 Japanese ancestry individuals NA Illumina [6108953] (imputed) 13 partial thromboplastin time http://www.ebi.ac.uk/efo/EFO_0004310 GCST006018 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Prothrombin time 58,110 Japanese ancestry individuals NA Illumina [6108953] (imputed) 14 prothrombin time measurement http://www.ebi.ac.uk/efo/EFO_0008390 GCST006017 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Fibrinogen levels 18,348 Japanese ancestry individuals NA Illumina [6108953] (imputed) 1 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST006015 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Creatine kinase levels 106,080 Japanese ancestry individuals NA Illumina [6108953] (imputed) 46 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST006014 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. Lactate dehydrogenase levels 126,319 Japanese ancestry individuals NA Illumina [6108953] (imputed) 14 L lactate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0004808 GCST006013 Genome-wide genotyping array 2018-07-28 29403010 Kanai M 2018-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29403010 Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. C-reactive protein levels 75,391 Japanese ancestry individuals NA Illumina [6108953] (imputed) 8 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST006012 Genome-wide genotyping array 2018-05-08 23143596 Eyre S 2012-12-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23143596 High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Rheumatoid arthritis up to 13,838 European ancestry cases, up to 33,742 European ancestry controls NA Illumina [129464] (imputed) 50 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST005569 Genome-wide genotyping array, Targeted genotyping array [ImmunoChip] 2018-05-08 23143596 Eyre S 2012-12-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23143596 High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Rheumatoid arthritis (ACPA-negative) 3,297 European ancestry cases, 15,870 European ancestry controls NA Illumina [129464] 2 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST005567 Targeted genotyping array [ImmunoChip] 2018-05-08 23143596 Eyre S 2012-12-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23143596 High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Rheumatoid arthritis (ACPA-positive) up to 9,585 European ancestry cases, up to 33,742 European ancestry controls NA Illumina [129464] (imputed) 56 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST005568 Genome-wide genotyping array, Targeted genotyping array [ImmunoChip] 2017-11-17 28957384 Kim SK 2017-09-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28957384 Two genetic loci associated with ankle injury. Ankle injury 1,421 European ancestry cases, 154 Hispanic/Latino cases, 121 East Asian ancestry cases, 81,843 European ancestry controls, 8,406 Hispanic/Latino controls, 7,397 East Asian ancestry controls NA Affymetrix [8183964] (imputed) 42 ankle injury http://www.ebi.ac.uk/efo/EFO_1002021 GCST004952 Genome-wide genotyping array 2018-09-20 29532581 Hallfors J 2018-03-13 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29532581 Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway. Smoking behaviour (cigarettes smoked per day) 1,715 Finnish ancestry ever smoker individuals from 739 families 7,344 Finnish ancestry ever smoker individuals Illumina [9469131] (imputed) 0 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST006299 Genome-wide genotyping array 2018-09-20 29532581 Hallfors J 2018-03-13 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29532581 Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway. Smoking behaviour (maximum cigarettes in a 24 hour period) 1,711 Finnish ancestry ever smoker individuals from up to 739 families NA Illumina [9469131] (imputed) 12 maximum cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0009264 GCST006300 Genome-wide genotyping array 2018-09-20 29532581 Hallfors J 2018-03-13 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29532581 Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway. Nicotine dependence symptom count 1,715 Finnish ancestry ever smoker individuals from 739 families NA Illumina [9469131] (imputed) 35 nicotine dependence symptom count http://www.ebi.ac.uk/efo/EFO_0009262 GCST006301 Genome-wide genotyping array 2018-09-20 29532581 Hallfors J 2018-03-13 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29532581 Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway. Nicotine dependence 873 Finnish ancestry cases and 842 Finnish ancestry controls from 739 families NA Illumina [9469131] (imputed) 16 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST006302 Genome-wide genotyping array 2018-09-20 29532581 Hallfors J 2018-03-13 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29532581 Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway. Nicotine withdrawal symptom count 1,703 Finnish ancestry ever smoker individuals from up to 739 families NA Illumina [9469131] (imputed) 25 nicotine withdrawal symptom count http://www.ebi.ac.uk/efo/EFO_0009263 GCST006303 Genome-wide genotyping array 2019-01-11 29532581 Hallfors J 2018-03-13 Addict Biol www.ncbi.nlm.nih.gov/pubmed/29532581 Genome-wide association study in Finnish twins highlights the connection between nicotine addiction and neurotrophin signaling pathway. Nicotine withdrawal 540 Finnish ancestry cases and 1,163 Finnish ancestry controls from up to 739 families NA Illumina [9469131] (imputed) 18 nicotine withdrawal measurement http://www.ebi.ac.uk/efo/EFO_0009362 GCST006869 Genome-wide genotyping array 2018-06-22 29545823 O'Brien KM 2018-03-01 Front Genet www.ncbi.nlm.nih.gov/pubmed/29545823 Genome-Wide Association Study of Serum 25-Hydroxyvitamin D in US Women. Serum 25-Hydroxyvitamin D levels 1,576 European ancestry individuals, 134 African American individuals, 81 Hispanic individuals, 38 individuals 1,307 European ancestry individuals, 722 European breast cancer cases, 693 European ancestry controls, 120 African-American individuals, 38 African American breast cancer cases, 46 African American controls, 59 Hispanic individuals, 27 Hispanic breast cancer cases, 27 Hispanic controls, 47 individuals, 23 breast cancer cases, 14 controls Illumina [386449] 2 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST005729 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Esophageal adenocarcinoma x smoking interaction 2,284 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 2 esophageal adenocarcinoma, smoking status measurement http://www.ebi.ac.uk/efo/EFO_0000478, http://www.ebi.ac.uk/efo/EFO_0006527 GCST006530 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Esophageal adenocarcinoma x pack-years of smoking exposure interaction 2,284 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 1 esophageal adenocarcinoma, pack-years measurement http://www.ebi.ac.uk/efo/EFO_0000478, http://www.ebi.ac.uk/efo/EFO_0006526 GCST006532 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Esophageal adenocarcinoma x gastroesophageal reflux disease interaction 2,284 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 3 esophageal adenocarcinoma, gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0000478, http://www.ebi.ac.uk/efo/EFO_0003948 GCST006531 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Barrett's esophagus x BMI interaction 3,104 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 1 Barrett's esophagus, body mass index http://www.ebi.ac.uk/efo/EFO_0000280, http://www.ebi.ac.uk/efo/EFO_0004340 GCST006529 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Barrett's esophagus x pack-years of smoking exposure interaction 3,104 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 4 pack-years measurement, Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0006526, http://www.ebi.ac.uk/efo/EFO_0000280 GCST006528 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Barrett's esophagus x smoking interaction 3,104 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 0 smoking status measurement, Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000280 GCST006527 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Barrett's esophagus x gastroesophageal reflux disease interaction 3,104 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 0 Barrett's esophagus, gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0000280, http://www.ebi.ac.uk/efo/EFO_0003948 GCST006526 Genome-wide genotyping array 2018-11-09 29551738 Dong J 2018-03-15 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29551738 Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Esophageal adenocarcinoma x BMI interaction 2,284 European ancestry cases, 2,182 European ancestry controls NA Illumina [993501] 0 esophageal adenocarcinoma, body mass index http://www.ebi.ac.uk/efo/EFO_0000478, http://www.ebi.ac.uk/efo/EFO_0004340 GCST006525 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Bacterial meningitis 1,149 European and unknown ancestry cases, 4,836 European and unknown ancestry controls NA Illumina [6800000] (imputed) 1 bacterial meningitis http://www.ebi.ac.uk/efo/EFO_1000831 GCST009083 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Pneumococcal meningitis x streptococcus pneumoniae genotype cluster interaction up to 145 European and unknown ancestry individuals NA Illumina [6800000] (imputed) 1 pneumococcal meningitis, bacterial pathogen genotype measurement http://www.ebi.ac.uk/efo/EFO_1001114, http://www.ebi.ac.uk/efo/EFO_0010271 GCST009082 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Pneumococcal meningitis x streptococcus pneumoniae antigen allele interaction up to 347 European and unknown ancestry individuals NA Illumina [6800000] (imputed) 2 pneumococcal meningitis, bacterial pathogen genotype measurement http://www.ebi.ac.uk/efo/EFO_1001114, http://www.ebi.ac.uk/efo/EFO_0010271 GCST009084 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Bacterial meningitis 2,345 European and unknown ancestry cases, 345,042 European and unknown ancestry controls NA Affymetrix, Illumina [6800000] (imputed) 1 bacterial meningitis http://www.ebi.ac.uk/efo/EFO_1000831 GCST009085 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Pneumococcal meningitis 732 European and unknown ancestry cases, 4,836 European and unknown ancestry controls NA Illumina [6800000] (imputed) 4 pneumococcal meningitis http://www.ebi.ac.uk/efo/EFO_1001114 GCST009086 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Pneumococcal meningitis 353 European ancestry cases, 3,278 European ancestry controls NA Illumina [6800000] (imputed) 1 pneumococcal meningitis http://www.ebi.ac.uk/efo/EFO_1001114 GCST009087 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Severe bacterial meningitis 277 European and unknown ancestry cases, 4,836 European and unknown ancestry controls NA Illumina [6800000] (imputed) 3 bacterial meningitis http://www.ebi.ac.uk/efo/EFO_1000831 GCST009088 Genome-wide genotyping array 2019-11-22 31092817 Lees JA 2019-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31092817 Joint sequencing of human and pathogen genomes reveals the genetics of pneumococcal meningitis. Pneumococcal bacteremia 873 European ancestry cases, 3,278 European ancestry controls NA Illumina [6800000] (imputed) 0 pneumococcal bacteremia http://www.ebi.ac.uk/efo/EFO_1001925 GCST009089 Genome-wide genotyping array 2018-07-20 29551627 Hawcutt DB 2018-03-15 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/29551627 Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. Corticosteroid-induced adrenal suppression (peak cortisol < 350 nmol/L) up to 35 European ancestry child cases with asthma, at least 372 European ancestry child controls with asthma, general adult population controls 6 child cases with asthma, 75 child controls with asthma Illumina [430492] 1 adrenal suppression measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0009176, http://purl.obolibrary.org/obo/GO_0031960 GCST005927 Genome-wide genotyping array 2018-07-20 29551627 Hawcutt DB 2018-03-15 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/29551627 Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. Corticosteroid-induced adrenal suppression (peak cortisol < 500 nmol/L) up to 175 European ancestry child cases with asthma, at least 232 European ancestry child controls with asthma, general adult population controls 32 child cases with asthma, 49 child controls with asthma, 17 adult cases with COPD, 61 adult controls with COPD Illumina [430492] 1 adrenal suppression measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0009176, http://purl.obolibrary.org/obo/GO_0031960 GCST005924 Genome-wide genotyping array 2018-07-20 29551627 Hawcutt DB 2018-03-15 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/29551627 Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. Baseline cortisol levels in response to low dose short synacthen test in corticosteroid treated asthma 407 European ancestry child cases NA Illumina [430492] 4 cortisol measurement, response to corticosteroid, response to synacthen http://www.ebi.ac.uk/efo/EFO_0005843, http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0009175 GCST005925 Genome-wide genotyping array 2018-07-20 29551627 Hawcutt DB 2018-03-15 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/29551627 Susceptibility to corticosteroid-induced adrenal suppression: a genome-wide association study. Peak cortisol response to low dose short synacthen test in corticosteroid treated asthma 407 European ancestry child cases NA Illumina [430492] 6 cortisol measurement, response to corticosteroid, response to synacthen http://www.ebi.ac.uk/efo/EFO_0005843, http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0009175 GCST005926 Genome-wide genotyping array 2018-05-02 29535370 Kleinstein SE 2018-02-28 Genes Immun www.ncbi.nlm.nih.gov/pubmed/29535370 Genome-wide association study (GWAS) of human host factors influencing viral severity of herpes simplex virus type 2 (HSV-2). Virologic severity in Herpes simplex virus type 2 infection 223 European ancestry individuals NA Illumina [1539908] 12 HSV2 virologic severity measurement http://www.ebi.ac.uk/efo/EFO_0009010 GCST005559 Genome-wide genotyping array 2018-05-30 29535761 Haaland OA 2018-02-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/29535761 A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG. Cleft lip with or without cleft palate (maternal periconceptional vitamin use interaction) up to 825 European ancestry case-parent trios, up to 1,024 Asian ancestry case-parent trios, up to 59 case-parent trios NA Illumina [341191] 8 vitamin supplement exposure measurement, cleft lip http://www.ebi.ac.uk/efo/EFO_0009116, http://www.ebi.ac.uk/efo/EFO_0003959 GCST005652 Genome-wide genotyping array 2018-05-30 29535761 Haaland OA 2018-02-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/29535761 A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG. Cleft lip with or without cleft palate (maternal periconceptional cigarette smoking interaction) up to 825 European ancestry case-parent trios, up to 1,024 Asian ancestry case-parent trios, up to 59 case-parent trios NA Illumina [341191] 1 tobacco smoke exposure measurement, cleft lip http://www.ebi.ac.uk/efo/EFO_0009115, http://www.ebi.ac.uk/efo/EFO_0003959 GCST005654 Genome-wide genotyping array 2018-05-30 29535761 Haaland OA 2018-02-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/29535761 A Genome-Wide Search for Gene-Environment Effects in Isolated Cleft Lip with or without Cleft Palate Triads Points to an Interaction between Maternal Periconceptional Vitamin Use and Variants in ESRRG. Cleft lip with or without cleft palate (maternal periconceptional alcohol intake interaction) up to 825 European ancestry case-parent trios, up to 1,024 Asian ancestry case-parent trios, up to 59 case-parent trios NA Illumina [341191] 2 cleft lip, alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0003959, http://www.ebi.ac.uk/efo/EFO_0009113 GCST005653 Genome-wide genotyping array 2018-05-18 29514873 Mychaleckyj JC 2018-03-07 J Med Genet www.ncbi.nlm.nih.gov/pubmed/29514873 Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of FADS1 variants to arachidonic acid, a critical infant micronutrient. Breast milk fatty acid composition (maternal genotype effect) 1,142 Bangladeshi ancestry (non-array genotyped, whole-genome imputed) mothers NA Illumina [~ 932000] (imputed) 10 fatty acid measurement, breast milk measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0009092, http://www.ebi.ac.uk/efo/EFO_0005939 GCST005586 Genome-wide genotyping array 2018-05-18 29514873 Mychaleckyj JC 2018-03-07 J Med Genet www.ncbi.nlm.nih.gov/pubmed/29514873 Multiplex genomewide association analysis of breast milk fatty acid composition extends the phenotypic association and potential selection of FADS1 variants to arachidonic acid, a critical infant micronutrient. Breast milk fatty acid composition (infant genotype effect) 1,142 Bangladeshi ancestry infants NA Illumina [~ 932000] 8 fatty acid measurement, fetal genotype effect measurement, breast milk measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0009092 GCST005587 Genome-wide genotyping array 2018-07-11 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Stroke 40,585 European ancestry cases, 406,111 European ancestry controls, 17,369 East Asian ancestry cases, 28,195 East Asian ancestry controls, 2,437 South Asian ancestry cases, 6,707 South Asian ancestry controls, 5,541 African American cases, 15,154 African American controls, 365 Asian ancestry cases, 333 Asian ancestry controls, 865 Latin American cases, 692 Latin American controls NA NR [~ 8000000] (imputed) 32 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST005838 Genome-wide genotyping array 2019-01-18 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Stroke 40,585 European ancestry cases, 406,111 European ancestry controls NA NR [~ 8000000] (imputed) 22 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST006906 Genome-wide genotyping array 2019-01-18 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke (large artery atherosclerosis) 4,373 European ancestry cases, 406,111 European ancestry controls NA NR [~ 8000000] (imputed) 6 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST006907 Genome-wide genotyping array 2019-01-18 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke 34,217 European ancestry cases, 406,111 European ancestry controls NA NR [~ 8000000] (imputed) 19 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST006908 Genome-wide genotyping array 2018-07-11 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke (large artery atherosclerosis) 4,373 European ancestry cases, 406,111 European ancestry controls, 1,626 East Asian ancestry cases, 28,195 East Asian ancestry controls, 355 South Asian ancestry cases, 6,707 South Asian ancestry controls, 259 African American cases, 15,146 African American controls, 34 Asian ancestry cases, 333 Asian ancestry controls, 41 Latin American cases, 692 Latin American controls NA NR [~ 8000000] (imputed) 8 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST005840 Genome-wide genotyping array 2018-07-11 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke (small-vessel) 5,386 European ancestry cases, 192,662 European ancestry controls, 5,096 East Asian ancestry cases, 28,195 East Asian ancestry controls, 314 South Asian ancestry cases, 6,707 South Asian ancestry controls, 694 African American cases, 15,146 African American controls, 134 Asian ancestry cases, 333 Asian ancestry controls, 86 Latin American cases, 692 Latin American controls NA NR [~ 8000000] (imputed) 9 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST005841 Genome-wide genotyping array 2018-07-11 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke (cardioembolic) 7,193 European ancestry cases, 406,111 European ancestry controls, 847 East Asian ancestry cases, 28,195 East Asian ancestry controls, 422 South Asian ancestry cases, 6,707 South Asian ancestry controls, 414 African American cases, 15,146 African American controls, 31 Asian ancestry cases, 333 Asian ancestry controls, 99 Latin American cases, 692 Latin American controls NA NR [~ 8000000] (imputed) 10 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST005842 Genome-wide genotyping array 2018-07-11 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke 34,217 European ancestry cases, 406,111 European ancestry controls, 17,369 East Asian ancestry cases, 28,195 East Asian ancestry controls, 2,437 South Asian ancestry cases, 6,707 South Asian ancestry controls, 5,541 African American cases, 15,146 African American controls, 222 Asian ancestry cases, 333 Asian ancestry controls, 555 Latin American cases, 692 Latin American controls NA NR [~ 8000000] (imputed) 28 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST005843 Genome-wide genotyping array 2019-01-18 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke (small-vessel) 5,386 European ancestry cases, 192,662 European ancestry controls NA NR [~ 8000000] (imputed) 2 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST006909 Genome-wide genotyping array 2019-01-18 29531354 Malik R 2018-03-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29531354 Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Ischemic stroke (cardioembolic) 7,193 European ancestry cases, 406,111 European ancestry controls NA NR [~ 8000000] (imputed) 5 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST006910 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Triacylglyceride levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 21 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008922 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Ceramide levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST008923 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Diacylglyceride levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 2 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST008924 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Lysophosphatidylcholine levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 16 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST008925 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Lysophosphatidylethanolamine levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 7 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST008926 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Phosphatidylcholine levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 25 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST008927 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Phosphatidylcholine-ether levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 10 phosphatidylcholine ether measurement http://www.ebi.ac.uk/efo/EFO_0010227 GCST008928 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Phosphatidylethanolamine levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 12 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST008929 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Phosphatidylethanolamine-ether levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 4 phosphatidylethanolamine ether measurement http://www.ebi.ac.uk/efo/EFO_0010229 GCST008930 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Phosphatidylinositol levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 9 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST008931 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Cholesteryl ester levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 11 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST008932 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Sphingomyelin levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 22 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST008933 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Sterol levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 0 sterol measurement http://www.ebi.ac.uk/efo/EFO_0010231 GCST008934 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Low density lipoprotein cholesterol levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008935 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. High density lipoprotein cholesterol levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008936 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Triglyceride levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008937 Genome-wide genotyping array 2019-10-25 31551469 Tabassum R 2019-09-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31551469 Genetic architecture of human plasma lipidome and its link to cardiovascular disease. Total cholesterol levels 2,045 European ancestry individuals NA Illumina [~ 9300000] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST008938 Genome-wide genotyping array 2019-03-28 30631343 Rolfe S 2018-12-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/30631343 Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry. Normal facial asymmetry (angle of surface orientation score) 3,186 European ancestry individuals NA Illumina [747780] 21 facial asymmetry measurement http://www.ebi.ac.uk/efo/EFO_0009751 GCST007448 Genome-wide genotyping array 2019-03-28 30631343 Rolfe S 2018-12-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/30631343 Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry. Normal facial asymmetry (angle of deformation score) 3,186 European ancestry individuals NA Illumina [747780] 4 facial asymmetry measurement http://www.ebi.ac.uk/efo/EFO_0009751 GCST007449 Genome-wide genotyping array 2019-03-28 30631343 Rolfe S 2018-12-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/30631343 Associations Between Genetic Data and Quantitative Assessment of Normal Facial Asymmetry. Normal facial asymmetry (deformation magnitude) 3,186 European ancestry individuals NA Illumina [747780] 5 facial asymmetry measurement http://www.ebi.ac.uk/efo/EFO_0009751 GCST007450 Genome-wide genotyping array 2017-03-27 27506219 Wang W 2016-08-09 Reprod Sci www.ncbi.nlm.nih.gov/pubmed/27506219 Pooling-Based Genome-Wide Association Study Identifies Risk Loci in the Pathogenesis of Ovarian Endometrioma in Chinese Han Women. Endometriosis 50 Chinese Han ancestry cases, 50 Chinese Han ancestry uterine myoma or hydrosalpinx controls 1,466 Chinese Han ancestry cases, 1,410 Chinese Han ancestry uterine myoma or hydrosalpinx controls Affymetrix [906600] 4 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST003819 Genome-wide genotyping array 2018-06-29 29547969 Chen X 2018-03-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29547969 A genome-wide association study of IgM antibody against phosphorylcholine: shared genetics and phenotypic relation to chronic lymphocytic leukemia. Immunoglobulin M against phosphorylcholine (IgM anti-PC) levels 3,002 European ancestry individuals 646 European ancestry individuals Illumina [NR] (imputed) 1 serum IgM measurement http://www.ebi.ac.uk/efo/EFO_0004993 GCST005761 Genome-wide genotyping array 2018-05-21 29534301 Nishida N 2018-03-13 Hepatology www.ncbi.nlm.nih.gov/pubmed/29534301 Key HLA-DRB1-DQB1 haplotypes and role of the BTNL2 gene for response to a hepatitis B vaccine. Response to hepatitis B vaccine 107 Japanese ancestry low responder individuals, 351 Japanese ancestry intermediate responder individuals, 735 Japanese ancestry high responder individuals NA Affymetrix [427664] 20 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST005606 Genome-wide genotyping array 2019-03-18 30617256 Jansen IE 2019-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30617256 Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. Alzheimer's disease (late onset) 24,087 European ancestry cases, 55,058 European ancestry controls NA Illumina [up to 9862738] (imputed) 33 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST007319 Genome-wide genotyping array, Exome-wide sequencing 2019-03-18 30617256 Jansen IE 2019-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30617256 Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. Family history of Alzheimer's disease 47,793 European ancestry cases, 328,320 European ancestry controls NA Affymetrix [10847151] (imputed) 33 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST007321 Genome-wide genotyping array 2019-03-18 30617256 Jansen IE 2019-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30617256 Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer's disease risk. Alzheimer's disease or family history of Alzheimer's disease 24,087 European ancestry late-onset Alzheimer's disease cases, 47,793 European ancestry individuals with family history of Alzheimer's disease, 383,378 European ancestry controls NA Affymetrix, Illumina [up to 10847151] (imputed) 108 Alzheimer disease, family history of Alzheimer’s disease http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0009268 GCST007320 Genome-wide genotyping array, Exome-wide sequencing 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and systolic blood pressure (pleiotropy) 230,204 individuals NA NR [2382073] 3 systolic blood pressure, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0006335, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007125 Genome-wide genotyping array 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and body mass index (pleiotropy) 151,013 individuals NA NR [2400377] 1 body mass index, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0004340, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007126 Genome-wide genotyping array 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and waist-to-hip-ratio (pleiotropy) 104,315 individuals NA NR [2376820] 1 waist-hip ratio, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0004343, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007127 Genome-wide genotyping array 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and type 2 diabetes (pleiotropy) 49,192 individuals NA NR [2426886] 2 type 2 diabetes mellitus, multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005148, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007120 Genome-wide genotyping array 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and C-reactive protein levels (pleiotropy) 93,333 individuals NA NR [2418544] 3 C-reactive protein measurement, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0004458, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007121 Genome-wide genotyping array 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and triglyceride levels (pleiotropy) 215,725 individuals NA NR [2487152] 6 triglyceride measurement, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0004530, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007122 Genome-wide genotyping array 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and LDL levels (pleiotropy) 215,725 individuals NA NR [2491989] 4 low density lipoprotein cholesterol measurement, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0004611, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007123 Genome-wide genotyping array 2019-02-12 26920376 Wang Y 2016-02-26 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26920376 Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors. Multiple sclerosis and HDL levels (pleiotropy) 215,725 individuals NA NR [2492237] 7 high density lipoprotein cholesterol measurement, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0004612, http://purl.obolibrary.org/obo/MONDO_0005301 GCST007124 Genome-wide genotyping array 2019-02-01 30621171 Coltell O 2019-01-04 Nutrients www.ncbi.nlm.nih.gov/pubmed/30621171 Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population. Serum bilirubin levels in metabolic syndrome 188 European ancestry male individuals, 242 European ancestry female individuals NA Illumina [622468] 23 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST007018 Genome-wide genotyping array 2019-02-01 30621171 Coltell O 2019-01-04 Nutrients www.ncbi.nlm.nih.gov/pubmed/30621171 Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population. Serum bilirubin levels x sex interaction in metabolic syndrome 188 European ancestry male individuals, 242 European ancestry female individuals NA Illumina [622468] 16 sex interaction measurement, bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004570 GCST007016 Genome-wide genotyping array 2019-02-01 30621171 Coltell O 2019-01-04 Nutrients www.ncbi.nlm.nih.gov/pubmed/30621171 Genome-Wide Association Study (GWAS) on Bilirubin Concentrations in Subjects with Metabolic Syndrome: Sex-Specific GWAS Analysis and Gene-Diet Interactions in a Mediterranean Population. Serum bilirubin levels x Mediterranean diet adherence interaction in metabolic syndrome 257 European ancestry individuals with low adherence to Mediterranean diet, 161 European ancestry individuals with high adherence to Mediterranean diet NA Illumina [622468] 26 diet measurement, bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004570 GCST007017 Genome-wide genotyping array 2018-10-09 29779033 Hishida A 2018-05-18 Am J Nephrol www.ncbi.nlm.nih.gov/pubmed/29779033 Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study. Chronic kidney disease 939 Japanese ancestry cases, 10,344 Japanese ancestry controls 38,143 Japanese ancestry cases, 110,686 Japanese ancestry controls Illumina [6288024] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST006391 Genome-wide genotyping array 2018-10-09 29779033 Hishida A 2018-05-18 Am J Nephrol www.ncbi.nlm.nih.gov/pubmed/29779033 Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study. Estimated glomerular filtration rate 11,283 Japanese ancestry individuals 148,829 Japanese ancestry individuals Illumina [6288024] (imputed) 4 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST006392 Genome-wide genotyping array 2018-10-09 29779033 Hishida A 2018-05-18 Am J Nephrol www.ncbi.nlm.nih.gov/pubmed/29779033 Genome-Wide Association Study of Renal Function Traits: Results from the Japan Multi-Institutional Collaborative Cohort Study. Serum creatinine levels 11,283 Japanese ancestry individuals 148,829 Japanese ancestry individuals Illumina [6288024] (imputed) 4 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST006393 Genome-wide genotyping array 2021-01-28 32339537 Roberts V 2020-04-24 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/32339537 Genome wide association study identifies genetic associations with perceived age. Youthful appearance (self-reported) 423,992 European ancestry individuals NA Affymetrix [~ 9600000] (imputed) 81 skin aging measurement http://www.ebi.ac.uk/efo/EFO_0008006 GCST011011 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in chylomicrons and extremely large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091645 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting chylomicrons and extremely large VLDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091646 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in chylomicrons and extremely large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091647 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in chylomicrons and extremely large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 2 chylomicron measurement, triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091648 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial apolipoprotein A-I 4,348 individuals NA Illumina [7701709] (imputed) 5 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90091649 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial apolipoprotein B 4,348 individuals NA Illumina [7701709] (imputed) 5 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90091650 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial 3-hydroxybutyrate 4,348 individuals NA Illumina [7701709] (imputed) 1 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90091651 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial citrate 4,348 individuals NA Illumina [7701709] (imputed) 3 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90091652 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial conjugated linoleic acid 4,348 individuals NA Illumina [7701709] (imputed) 1 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90091653 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial docosahexaenoic acid (22:6) 4,348 individuals NA Illumina [7701709] (imputed) 3 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90091654 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial esterified cholesterol 4,348 individuals NA Illumina [7701709] (imputed) 6 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091655 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial estimated description of fatty acid chain length (not actual carbon number) 4,348 individuals NA Illumina [7701709] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091656 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial omega-3 fatty acids 4,348 individuals NA Illumina [7701709] (imputed) 3 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90091657 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial omega-6 fatty acids 4,348 individuals NA Illumina [7701709] (imputed) 7 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90091658 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol 4,348 individuals NA Illumina [7701709] (imputed) 8 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90091659 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial glutamine 4,348 individuals NA Illumina [7701709] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90091660 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial glycoprotein acetyls (mainly a1-acid glycoprotein) 4,348 individuals NA Illumina [7701709] (imputed) 3 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90091661 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in HDL2 4,348 individuals NA Illumina [7701709] (imputed) 5 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091662 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in HDL3 4,348 individuals NA Illumina [7701709] (imputed) 5 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091663 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in HDL 4,348 individuals NA Illumina [7701709] (imputed) 4 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091664 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial mean diameter of HDL particles 4,348 individuals NA Illumina [7701709] (imputed) 7 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90091665 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides in HDL 4,348 individuals NA Illumina [7701709] (imputed) 5 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091666 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in IDL 4,348 individuals NA Illumina [7701709] (imputed) 7 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091667 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in IDL 4,348 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091668 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in IDL 4,348 individuals NA Illumina [7701709] (imputed) 7 free cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091669 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in IDL 4,348 individuals NA Illumina [7701709] (imputed) 8 lipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091670 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial IDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 8 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091671 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in IDL 4,348 individuals NA Illumina [7701709] (imputed) 9 phospholipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091672 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in IDL 4,348 individuals NA Illumina [7701709] (imputed) 6 triglyceride measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091673 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial isoleucine 4,348 individuals NA Illumina [7701709] (imputed) 2 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90091674 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial linoleic acid (18:2) 4,348 individuals NA Illumina [7701709] (imputed) 6 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90091675 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091676 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial mean diameter of LDL particles 4,348 individuals NA Illumina [7701709] (imputed) 4 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90091677 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides in LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091678 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial leucine 4,348 individuals NA Illumina [7701709] (imputed) 1 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90091679 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in large HDL 4,348 individuals NA Illumina [7701709] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091680 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in large HDL 4,348 individuals NA Illumina [7701709] (imputed) 4 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091681 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in large HDL 4,348 individuals NA Illumina [7701709] (imputed) 3 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091682 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in large HDL 4,348 individuals NA Illumina [7701709] (imputed) 4 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091683 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial large HDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091684 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in large HDL 4,348 individuals NA Illumina [7701709] (imputed) 3 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091685 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in large HDL 4,348 individuals NA Illumina [7701709] (imputed) 5 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091686 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in large LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091687 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in large LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091688 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in large LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091689 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in large LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091690 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial large LDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091691 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in large LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091692 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in large LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091693 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091694 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 3 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091695 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 5 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091696 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091697 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial large VLDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091698 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091699 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091700 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in medium HDL 4,348 individuals NA Illumina [7701709] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091701 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in medium HDL 4,348 individuals NA Illumina [7701709] (imputed) 3 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091702 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in medium HDL 4,348 individuals NA Illumina [7701709] (imputed) 4 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091703 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in medium HDL 4,348 individuals NA Illumina [7701709] (imputed) 3 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091704 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial medium HDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091705 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in medium HDL 4,348 individuals NA Illumina [7701709] (imputed) 4 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091706 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in medium HDL 4,348 individuals NA Illumina [7701709] (imputed) 6 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091707 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in medium LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091708 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in medium LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091709 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in medium LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091710 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in medium LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091711 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial medium LDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091712 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in medium LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091713 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in medium LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091714 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial monounsaturated fatty acids (16:1, 18:1) 4,348 individuals NA Illumina [7701709] (imputed) 6 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091715 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in medium VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091716 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in medium VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091717 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in medium VLDL 4,348 individuals NA Illumina [7701709] (imputed) 5 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091718 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in medium VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091719 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in very large HDL 4,734 individuals NA Illumina [7701709] (imputed) 9 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091624 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting very large HDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091625 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in very large HDL 4,734 individuals NA Illumina [7701709] (imputed) 7 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091626 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in very large HDL 4,734 individuals NA Illumina [7701709] (imputed) 6 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091627 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in very large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 2 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091628 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in very large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 3 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091629 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in very large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 2 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091630 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in very large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 3 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091631 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting very large VLDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 3 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091632 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in very large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091633 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in very large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 3 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091634 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in very small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 8 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091635 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in very small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 8 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091636 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in very small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 9 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091637 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in very small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 11 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091638 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting very small VLDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 8 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091639 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in very small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 10 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091640 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in very small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 6 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091641 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in chylomicrons and extremely large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091642 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in chylomicrons and extremely large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091643 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in chylomicrons and extremely large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 2 free cholesterol measurement, chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091644 Genome-wide genotyping array 2018-10-16 29743933 Wu B 2018-03-18 Comput Math Methods Med www.ncbi.nlm.nih.gov/pubmed/29743933 Fast and Accurate Genome-Wide Association Test of Multiple Quantitative Traits. Glycemic traits (multi-trait analysis) 5,947 European ancestry individuals NA NR [~ 2500000] (imputed) 5 fasting blood glucose measurement, glucose tolerance test, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004465, http://www.ebi.ac.uk/efo/EFO_0004307, http://www.ebi.ac.uk/efo/EFO_0004466 GCST006404 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides in VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091620 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in very large HDL 4,734 individuals NA Illumina [7701709] (imputed) 7 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091621 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in very large HDL 4,734 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091622 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in very large HDL 4,734 individuals NA Illumina [7701709] (imputed) 9 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091623 Genome-wide genotyping array 2018-09-18 30013178 Kowalec K 2018-07-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30013178 Common variation near IRF6 is associated with IFN-β-induced liver injury in multiple sclerosis. Drug-induced liver injury in interferon-beta-treated multiple sclerosis 38 European ancestry cases, 113 European ancestry controls 18 European ancestry cases, 13 European ancestry controls Illumina [up to 1705969] (imputed) 1 response to interferon-beta, drug-induced liver injury http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0004228 GCST006270 Genome-wide genotyping array 2018-06-21 29751835 Hu H 2018-05-11 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/29751835 Genome-wide association study identified ATP6V1H locus influencing cerebrospinal fluid BACE activity. Cerebrospinal fluid beta-site APP cleaving enzyme levels 86 European ancestry Alzheimer's disease cases, 163 European ancestry mild cognitive impairment cases, 91 European ancestry controls NR Illumina [519442] 8 beta-secretase 1 measurement http://www.ebi.ac.uk/efo/EFO_0009179 GCST005714 Genome-wide genotyping array 2020-01-21 31809533 Han X 2019-09-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31809533 Genome-wide association analysis of 95 549 individuals identifies novel loci and genes influencing optic disc morphology. Optic disc size 67,040 British ancestry individuals 28,509 European ancestry individuals Affymetrix [8928767] (imputed) 115 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST009462 Genome-wide genotyping array 2020-05-28 32231278 Hysi PG 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231278 Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. Refractive error 542,934 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 448 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST010002 Genome-wide genotyping array 2020-05-28 32231278 Hysi PG 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231278 Meta-analysis of 542,934 subjects of European ancestry identifies new genes and mechanisms predisposing to refractive error and myopia. Refractive error 351,091 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST010003 Genome-wide genotyping array 2020-01-29 31712720 Forstner AJ 2019-11-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31712720 Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. Panic disorder 2,147 European ancestry cases, 7,760 European ancestry controls 2,408 European ancestry cases, 228,470 European ancestry controls Illumina [8757275] (imputed) 5 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST009525 Genome-wide genotyping array 2020-07-23 32321835 Alic L 2020-04-22 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/32321835 A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes. Complement factor H binding to malondialdehyde 896 European ancestry major depressive disorder cases, 934 European ancestry individuals NA Illumina [4278941] (imputed) 5 complement factor H measurement, protein binding measurement http://www.ebi.ac.uk/efo/EFO_0008097, http://www.ebi.ac.uk/efo/EFO_0010742 GCST010306 Genome-wide genotyping array 2020-07-23 32321835 Alic L 2020-04-22 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/32321835 A genome-wide association study identifies key modulators of complement factor H binding to malondialdehyde-epitopes. Complement factor H binding to malondialdehyde 934 European ancestry individuals NA Illumina [4278941] (imputed) 5 complement factor H measurement, protein binding measurement http://www.ebi.ac.uk/efo/EFO_0008097, http://www.ebi.ac.uk/efo/EFO_0010742 GCST010305 Genome-wide genotyping array 2020-08-03 32352494 Han X 2020-04-30 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/32352494 Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study. Retinal detachment 4,257 European ancestry cases, 39,181 European ancestry controls NA NR [NR] 2 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST010377 Genome-wide genotyping array 2020-08-03 32352494 Han X 2020-04-30 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/32352494 Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study. Spherical equivalent 95,827 European ancestry individuals NA NR [NR] 224 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST010378 Genome-wide genotyping array 2020-08-03 32352494 Han X 2020-04-30 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/32352494 Association of Myopia and Intraocular Pressure With Retinal Detachment in European Descent Participants of the UK Biobank Cohort: A Mendelian Randomization Study. Intraocular pressure 101,939 European ancestry cases NA NR [NR] 99 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST010376 Genome-wide genotyping array 2021-01-06 29874175 Bihlmeyer NA 2018-01-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/29874175 ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals. QT interval 83,884 European ancestry individuals, 9,610 African American individuals, 1,382 Hispanic individuals, 750 East Asian ancestry individuals. NA Illumina [up to 209449] 29 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST010919 Exome genotyping array 2021-01-06 29874175 Bihlmeyer NA 2018-01-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/29874175 ExomeChip-Wide Analysis of 95 626 Individuals Identifies 10 Novel Loci Associated With QT and JT Intervals. JT interval up to 83,884 European ancestry individuals, up to 9,610 African American individuals, up to 1,382 Hispanic individuals, up to750 East Asian ancestry individuals. NA Illumina [up to 209449] 4 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST010918 Exome genotyping array 2019-05-10 30610197 Smeland OB 2019-01-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30610197 Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence. Bipolar disorder or intelligence (pleiotropy) 20,352 European ancestry bipolar disorder cases, 31,358 European ancestry controls, 269,867 individuals NA NR [9295119] (imputed) 0 bipolar disorder, intelligence http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0004337 GCST007781 Genome-wide genotyping array 2019-05-10 30610197 Smeland OB 2019-01-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30610197 Genome-wide analysis reveals extensive genetic overlap between schizophrenia, bipolar disorder, and intelligence. Schizophrenia or intelligence (pleiotropy) 35,476 European and East Asian ancestry schizophrenia cases, 46,839 European and East Asian ancestry controls, 269,867 individuals NA NR [9295119] (imputed) 0 schizophrenia, intelligence http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0004337 GCST007782 Genome-wide genotyping array 2021-05-14 32358372 Ouyang H 2020-05-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/32358372 Constructing gene network for type 1 narcolepsy based on genome-wide association study and differential gene expression analysis (STROBE). Narcolepsy with cataplexy 903 Chinese ancestry cases, 1,982 Chinese ancestry controls NA Affymetrix [237955] (imputed) 6 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST011662 Genome-wide genotyping array 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Sortilin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010173 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Lipoprotein lipase levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010149 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Serine/threonine-protein kinase 4 levels 1,095 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010175 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tyrosine-protein kinase Mer levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010151 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Matrix metalloproteinase-12 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010152 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Matrix metalloproteinase-7 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010153 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. NF-kappa-B essential modulator levels 1,298 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010154 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Pappalysin-1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010155 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Proteinase-activated receptor 1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010156 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Poly [ADP-ribose] polymerase 1 levels 823 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010157 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Platelet-derived growth factor subunit B levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010158 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Programmed cell death 1 ligand 2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010159 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Placenta growth factor levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010160 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Polymeric immunoglobulin receptor levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010161 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Prolargin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010162 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. V-set and immunoglobulin domain-containing protein 2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010187 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Prostasin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010164 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. P-selectin glycoprotein ligand 1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010165 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Pentraxin-related protein PTX3 levels 1,292 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010166 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Receptor for advanced glycosylation end products levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010167 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Renin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010168 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Stem cell factor levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010169 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Serpin A12 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010170 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. SLAM family member 7 levels 1,299 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010171 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-C motif chemokine 24 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010197 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Leptin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010148 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Spondin-2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010174 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Macrophage receptor MARCO levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010150 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tissue factor levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010176 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Protein-glutamine gamma-glutamyltransferase 2 levels 1,291 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010177 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Thrombospondin-2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010178 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Thrombopoietin levels 1,300 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010179 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Angiopoietin-1 receptor levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010180 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Thrombomodulin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010181 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor superfamily member 10A levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010182 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor superfamily member 11A levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010183 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor superfamily member 13B levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010184 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. TNF-related apoptosis-inducing ligand receptor 2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010185 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. vascular endothelial growth factor D levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010186 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Serine protease 27 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010163 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. XCL1 levels 1,280 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010188 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. CD166 antigen levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010189 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Aminopeptidase N levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010190 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tyrosine-protein kinase receptor UFO levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010191 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Azurocidin levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010192 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Bleomycin hydrolase levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010193 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Caspase-3 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010194 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-C motif chemokine 15 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010195 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-C motif chemokine 16 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010196 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Superoxide dismutase [Mn],mitochondrial levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010172 Genome-wide sequencing [22x] 2020-06-01 32173896 Maffioletti E 2020-03-16 Drug Dev Res www.ncbi.nlm.nih.gov/pubmed/32173896 Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response. Vascular endothelial growth factor levels in major depressive disorder 121 European ancestry individuals NA Illumina [677673] 1 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST010036 Genome-wide genotyping array 2020-06-01 32173896 Maffioletti E 2020-03-16 Drug Dev Res www.ncbi.nlm.nih.gov/pubmed/32173896 Genetic determinants of circulating VEGF levels in major depressive disorder and electroconvulsive therapy response. Vascular endothelial growth factor levels 145 European ancestry individuals NA Affymetrix [646354] 1 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST010037 Genome-wide genotyping array 2020-03-03 31996736 Elsheikh SSM 2020-01-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31996736 Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease. Longitudinal brain connectivity change (Louvain modularity) 57 European ancestry individuals NA NR [9015039] (imputed) 12 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST009730 Genome-wide genotyping array 2020-03-03 31996736 Elsheikh SSM 2020-01-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31996736 Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease. Longitudinal brain connectivity change (transitivity) 57 European ancestry individuals NA NR [9015039] (imputed) 8 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST009729 Genome-wide genotyping array 2020-03-03 31996736 Elsheikh SSM 2020-01-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31996736 Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease. Longitudinal brain connectivity change (global efficiency) 57 European ancestry individuals NA NR [9015039] (imputed) 7 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST009728 Genome-wide genotyping array 2020-03-03 31996736 Elsheikh SSM 2020-01-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31996736 Genome-Wide Association Study of Brain Connectivity Changes for Alzheimer's Disease. Longitudinal brain connectivity change (characteristic path length) 57 European ancestry individuals NA NR [9015039] (imputed) 4 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST009727 Genome-wide genotyping array 2018-11-09 29781551 Guo X 2018-05-21 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29781551 A univariate perspective of multivariate genome-wide association analysis. Axial length 1,055 individuals NA NR [500025] 1 axial length measurement http://www.ebi.ac.uk/efo/EFO_0005318 GCST006541 Genome-wide genotyping array 2018-11-09 29781551 Guo X 2018-05-21 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29781551 A univariate perspective of multivariate genome-wide association analysis. Spherical error 1,055 individuals NA NR [500025] 0 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST006539 Genome-wide genotyping array 2019-01-10 29781551 Guo X 2018-05-21 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29781551 A univariate perspective of multivariate genome-wide association analysis. Axial length or spherical error (univariate decomposition analysis) 1,055 individuals NA NR [500025] 5 axial length measurement, refractive error http://www.ebi.ac.uk/efo/EFO_0005318, http://purl.obolibrary.org/obo/MONDO_0004892 GCST006864 Genome-wide genotyping array 2020-01-30 31766143 Ortega-Azorin C 2019-11-13 Nutrients www.ncbi.nlm.nih.gov/pubmed/31766143 Candidate Gene and Genome-Wide Association Studies for Circulating Leptin Levels Reveal Population and Sex-Specific Associations in High Cardiovascular Risk Mediterranean Subjects. Circulating leptin levels in high cardiovascular risk 351 Spanish mediterranean ancestry men, 615 Spanish mediterranean ancestry women NA Illumina [628376] 25 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST009532 Genome-wide genotyping array 2020-01-30 31766143 Ortega-Azorin C 2019-11-13 Nutrients www.ncbi.nlm.nih.gov/pubmed/31766143 Candidate Gene and Genome-Wide Association Studies for Circulating Leptin Levels Reveal Population and Sex-Specific Associations in High Cardiovascular Risk Mediterranean Subjects. Circulating leptin levels x sex interaction in high cardiovascular risk 351 Spanish mediterranean ancestry men, 615 Spanish mediterranean ancestry women NA Illumina [628376] 5 leptin measurement, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0005000, http://www.ebi.ac.uk/efo/EFO_0008343 GCST009533 Genome-wide genotyping array 2020-03-04 32004448 Savage SA 2020-01-30 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32004448 Genome-wide Association Study Identifies HLA-DPB1 as a Significant Risk Factor for Severe Aplastic Anemia. Severe aplastic anemia 359 European ancestry cases, 1,396 European ancestry controls 175 European ancestry cases, 1,059 European ancestry controls Illumina [688067] 8 severe aplastic anemia http://www.ebi.ac.uk/efo/EFO_0006927 GCST009734 Genome-wide genotyping array 2020-05-13 32005204 Alblooshi H 2020-01-31 BMC Psychiatry www.ncbi.nlm.nih.gov/pubmed/32005204 Stratified analyses of genome wide association study data reveal haplotypes for a candidate gene on chromosome 2 (KIAA1211L) is associated with opioid use in patients of Arabian descent. Opioid use disorder 199 Arabian ancestry cases, 253 Arabian ancestry controls NA Illumina [1879623] 3 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST009964 Genome-wide genotyping array 2018-10-17 29785010 Khawaja AP 2018-05-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29785010 Genome-wide analyses identify 68 new loci associated with intraocular pressure and improve risk prediction for primary open-angle glaucoma. Intraocular pressure 139,555 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 133 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST006412 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting acetate 4,734 individuals NA Illumina [7701709] (imputed) 1 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90091505 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting alanine 4,734 individuals NA Illumina [7701709] (imputed) 1 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90091506 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting apolipoprotein A-I 4,734 individuals NA Illumina [7701709] (imputed) 6 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90091507 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting apolipoprotein B 4,734 individuals NA Illumina [7701709] (imputed) 7 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90091508 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting 3-hydroxybutyrate 4,734 individuals NA Illumina [7701709] (imputed) 1 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90091509 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting citrate 4,734 individuals NA Illumina [7701709] (imputed) 3 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90091510 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides in VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091760 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in very large HDL 4,348 individuals NA Illumina [7701709] (imputed) 6 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091761 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in very large HDL 4,348 individuals NA Illumina [7701709] (imputed) 6 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091762 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in very large HDL 4,348 individuals NA Illumina [7701709] (imputed) 7 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091763 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in very large HDL 4,348 individuals NA Illumina [7701709] (imputed) 7 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091764 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial very large HDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 7 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091765 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in very large HDL 4,348 individuals NA Illumina [7701709] (imputed) 6 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091766 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in very large HDL 4,348 individuals NA Illumina [7701709] (imputed) 7 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091767 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in very large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 3 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091768 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial mean diameter of VLDLD particles 4,348 individuals NA Illumina [7701709] (imputed) 6 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90091759 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting docosahexaenoic acid (22:6) 4,734 individuals NA Illumina [7701709] (imputed) 4 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90091511 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting esterified cholesterol 4,734 individuals NA Illumina [7701709] (imputed) 9 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091512 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting estimated description of fatty acid chain length (not actual carbon number) 4,734 individuals NA Illumina [7701709] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091513 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting omega-3 fatty acids 4,734 individuals NA Illumina [7701709] (imputed) 5 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90091514 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting omega-6 fatty acids 4,734 individuals NA Illumina [7701709] (imputed) 6 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90091515 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol 4,734 individuals NA Illumina [7701709] (imputed) 8 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90091516 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting glucose 4,734 individuals NA Illumina [7701709] (imputed) 4 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90091517 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting glutamine 4,734 individuals NA Illumina [7701709] (imputed) 2 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90091518 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting glycoprotein acetyls (mainly a1-acid glycoprotein) 4,734 individuals NA Illumina [7701709] (imputed) 4 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90091519 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in HDL2 4,734 individuals NA Illumina [7701709] (imputed) 6 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091520 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in HDL3 4,734 individuals NA Illumina [7701709] (imputed) 5 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091521 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in HDL 4,734 individuals NA Illumina [7701709] (imputed) 7 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091522 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting mean diameter of HDL particles 4,734 individuals NA Illumina [7701709] (imputed) 9 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90091523 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides in HDL 4,734 individuals NA Illumina [7701709] (imputed) 5 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091524 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting histidine 4,734 individuals NA Illumina [7701709] (imputed) 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90091525 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in IDL 4,734 individuals NA Illumina [7701709] (imputed) 8 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091526 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in IDL 4,734 individuals NA Illumina [7701709] (imputed) 8 esterified cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091527 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in IDL 4,734 individuals NA Illumina [7701709] (imputed) 8 free cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091528 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in IDL 4,734 individuals NA Illumina [7701709] (imputed) 8 lipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091529 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting IDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 8 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091530 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in IDL 4,734 individuals NA Illumina [7701709] (imputed) 8 phospholipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091531 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in IDL 4,734 individuals NA Illumina [7701709] (imputed) 6 triglyceride measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091532 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting isoleucine 4,734 individuals NA Illumina [7701709] (imputed) 3 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90091533 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting linoleic acid (18:2) 4,734 individuals NA Illumina [7701709] (imputed) 7 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90091534 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting lactate 4,734 individuals NA Illumina [7701709] (imputed) 2 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90091535 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091536 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting mean diameter of LDL particles 4,734 individuals NA Illumina [7701709] (imputed) 3 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90091537 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides in LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091538 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting leucine 4,734 individuals NA Illumina [7701709] (imputed) 2 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90091539 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in large HDL 4,734 individuals NA Illumina [7701709] (imputed) 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091540 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in large HDL 4,734 individuals NA Illumina [7701709] (imputed) 9 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091541 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in large HDL 4,734 individuals NA Illumina [7701709] (imputed) 8 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091542 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in large HDL 4,734 individuals NA Illumina [7701709] (imputed) 7 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091543 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting large HDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 7 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091544 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in large HDL 4,734 individuals NA Illumina [7701709] (imputed) 6 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091545 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in large HDL 4,734 individuals NA Illumina [7701709] (imputed) 5 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091546 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in large LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091547 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in large LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091548 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in large LDL 4,734 individuals NA Illumina [7701709] (imputed) 6 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091549 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in large LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091550 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting large LDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 8 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091551 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in large LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091552 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in large LDL 4,734 individuals NA Illumina [7701709] (imputed) 6 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091553 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091554 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091555 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091556 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091557 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting large VLDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091558 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091559 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in large VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091560 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in medium HDL 4,734 individuals NA Illumina [7701709] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091561 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in medium HDL 4,734 individuals NA Illumina [7701709] (imputed) 3 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091562 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in medium HDL 4,734 individuals NA Illumina [7701709] (imputed) 2 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091563 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in medium HDL 4,734 individuals NA Illumina [7701709] (imputed) 3 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091564 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting medium HDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091565 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in medium HDL 4,734 individuals NA Illumina [7701709] (imputed) 4 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091566 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in medium HDL 4,734 individuals NA Illumina [7701709] (imputed) 6 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091567 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in medium LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091568 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in medium LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091569 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Death 5,974 European ancestry cases, up to 27,457 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 0 dead http://purl.obolibrary.org/obo/PATO_0001422 GCST005762 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Body mass index up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST005769 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. C-reactive protein levels up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST005770 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Creatinine levels up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST005771 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Diastolic blood pressure up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 3 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST005772 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Lung function (forced vital capacity) up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST005773 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Heart rate up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 1 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST005774 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Hematocrit up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 1 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST005775 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. High density lipoprotein cholesterol levels up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST005776 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Systolic blood pressure up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 2 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST005777 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Total cholesterol levels up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 6 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST005781 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Triglyceride levels up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 10 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST005780 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Alzheimer's disease 883 European ancestry cases, up to 32,548 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST005779 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Atrial fibrillation 2,562 European ancestry cases, up to 30,869 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST005778 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Cancer 4,935 European ancestry cases, up to 28,496 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST005768 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Coronary heart disease 6,403 European ancestry cases, up to 27,028 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST005767 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Diabetes mellitus 4,315 European ancestry cases, up to 29,116 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 1 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST005766 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Heart failure 3,527 European ancestry cases, up to 29,904 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST005765 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Stroke 2,449 European ancestry cases, up to 30,982 European ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST005764 Genome-wide genotyping array 2018-07-02 29615537 Kulminski AM 2018-03-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29615537 Strong impact of natural-selection-free heterogeneity in genetics of age-related phenotypes. Blood glucose levels up to 33,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 2 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST005763 Genome-wide genotyping array 2018-08-13 29752348 Rutten-Jacobs LCA 2018-05-11 Stroke www.ncbi.nlm.nih.gov/pubmed/29752348 Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia. White matter integrity (fractional anisotropy) 8,239 European ancestry individuals NA Affymetrix [up to 39131578] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST006063 Genome-wide genotyping array 2018-08-13 29752348 Rutten-Jacobs LCA 2018-05-11 Stroke www.ncbi.nlm.nih.gov/pubmed/29752348 Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia. White matter integrity (mean diffusivity) 8,239 European ancestry individuals NA Affymetrix [up to 39131578] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST006064 Genome-wide genotyping array 2018-08-13 29752348 Rutten-Jacobs LCA 2018-05-11 Stroke www.ncbi.nlm.nih.gov/pubmed/29752348 Genetic Study of White Matter Integrity in UK Biobank (N=8448) and the Overlap With Stroke, Depression, and Dementia. White matter hyperintensity volume 8,429 European ancestry individuals NA Affymetrix [up to 39131578] (imputed) 4 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST006062 Genome-wide genotyping array 2018-06-26 29766673 Fusco JP 2018-05-15 Cancer Med www.ncbi.nlm.nih.gov/pubmed/29766673 Genomic characterization of individuals presenting extreme phenotypes of high and low risk to develop tobacco-induced lung cancer. Non-small cell lung cancer in heavy smokers 47 European ancestry early age cases, 48 European ancestry advanced age controls 78 European ancestry early age cases, 55 European ancestry advanced age controls Illumina [2318553] 0 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST005747 Genome-wide genotyping array 2018-11-15 26177304 Waterman M 2015-09-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/26177304 Predictors of Outcome in Ulcerative Colitis. Ulcerative colitis 507 European ancestry cases, 61 Asian ancestry cases, 7 American ancestry cases, 2 Hispanic ancestry cases, 24 cases Illumina [ImmunoChip] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST006583 Targeted genotyping array [ImmunoChip] 2018-10-31 29942085 Nagel M 2018-06-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29942085 Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. Depression 688,809 European ancestry individuals NA Affymetrix [10847151] (imputed) 82 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST006477 Genome-wide genotyping array 2018-10-31 29942085 Nagel M 2018-06-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29942085 Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. Depressed affect 357,957 European ancestry individuals NA Affymetrix [10847151] (imputed) 157 unipolar depression, mood disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004247 GCST006475 Genome-wide genotyping array 2018-10-31 29942085 Nagel M 2018-06-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29942085 Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. Worry 348,219 European ancestry individuals NA Affymetrix [10847151] (imputed) 147 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST006478 Genome-wide genotyping array 2018-10-31 29942085 Nagel M 2018-06-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29942085 Meta-analysis of genome-wide association studies for neuroticism in 449,484 individuals identifies novel genetic loci and pathways. Neuroticism 449,484 European ancestry individuals NA Affymetrix [10847151] (imputed) 371 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST006476 Genome-wide genotyping array 2018-09-13 29970928 Zhu Z 2018-07-03 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29970928 Multi-level genomic analyses suggest new genetic variants involved in human memory. Short-term memory (digit-span task) 1,621 Chinese ancestry individuals 2,788 Chinese ancestry individuals Illumina [830937] 0 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST006253 Genome-wide genotyping array 2018-09-13 29970928 Zhu Z 2018-07-03 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29970928 Multi-level genomic analyses suggest new genetic variants involved in human memory. Short-term memory (visuospatial task) 1,623 Chinese ancestry individuals 2,790 Chinese ancestry individuals Illumina [830937] 1 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST006254 Genome-wide genotyping array 2018-09-13 29970928 Zhu Z 2018-07-03 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29970928 Multi-level genomic analyses suggest new genetic variants involved in human memory. Short-term memory (shared component of digit-span and visuospatial tasks) up to 1,623 Chinese ancestry individuals up to 2,790 Chinese ancestry individuals Illumina [up to 38219282] (imputed) 0 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST006255 Genome-wide genotyping array 2018-09-13 29970928 Zhu Z 2018-07-03 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29970928 Multi-level genomic analyses suggest new genetic variants involved in human memory. Long-term memory (delayed word recall task) 1,522 Chinese ancestry individuals 1,862 Chinese ancestry individuals Illumina [up to 38219282] (imputed) 2 word list delayed recall measurement http://www.ebi.ac.uk/efo/EFO_0006805 GCST006256 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Mean diameter of HDL particles meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 high density lipoprotein particle size change measurement http://www.ebi.ac.uk/efo/EFO_0020866 GCST90095433 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Serum total cholesterol meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095434 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095435 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Remnant cholesterol meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 remnant cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020867 GCST90095436 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095437 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095438 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in HDL2 meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095439 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in HDL3 meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095440 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Esterified cholesterol meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095441 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095442 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Serum total triglycerides meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095443 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides in VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095444 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides in LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095445 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides in HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095446 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Diacylglycerol meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 diglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0020868 GCST90095447 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total phosphoglycerides meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 glycerophospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0020869 GCST90095448 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phosphatidylcholine and other cholines meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 phosphatidylcholine change measurement, choline change measurement http://www.ebi.ac.uk/efo/EFO_0020871, http://www.ebi.ac.uk/efo/EFO_0020870 GCST90095449 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Sphingomyelins meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 sphingomyelin change measurement http://www.ebi.ac.uk/efo/EFO_0020872 GCST90095450 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholines meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 choline change measurement http://www.ebi.ac.uk/efo/EFO_0020870 GCST90095451 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Apolipoprotein A-I meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 apolipoprotein A 1 change measurement http://www.ebi.ac.uk/efo/EFO_0020873 GCST90095452 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Apolipoprotein B meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 apolipoprotein B change measurement http://www.ebi.ac.uk/efo/EFO_0020874 GCST90095453 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total fatty acids meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095454 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Estimated description of fatty acid chain length (not actual carbon number) meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095455 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Estimated degree of unsaturation meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095456 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Docosahexaenoic acid (22:6) meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 docosahexaenoic acid change measurement http://www.ebi.ac.uk/efo/EFO_0020876 GCST90095457 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in small LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095408 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Very large HDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095409 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095410 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in very large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095411 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Large HDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095412 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095413 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095414 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095415 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095416 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095417 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095418 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Medium HDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095419 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in medium HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095420 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in medium HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095421 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in medium HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095422 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in medium HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095423 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in medium HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095424 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Small HDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095425 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in small HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095426 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in small HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095427 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in small HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095428 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in small HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095429 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Mean diameter of VLDLD particles meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095430 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Mean diameter of VLDLD particles meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein particle size change measurement http://www.ebi.ac.uk/efo/EFO_0020907 GCST90095431 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Mean diameter of LDL particles meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein particle size change measurement http://www.ebi.ac.uk/efo/EFO_0020908 GCST90095432 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in large LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST90095388 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in large LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095389 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in large LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095390 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in large LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095391 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in large LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095392 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in large LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095393 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in large LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095394 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in medium LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST90095395 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in medium LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095396 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in medium LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095397 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in medium LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095398 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in medium LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095399 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in medium LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095400 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in medium LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095401 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Small LDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST90095402 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in small LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095403 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in small LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095404 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in small LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095405 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in small LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095406 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in small LDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095407 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Linoleic acid (18:2) meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 linoleic acid change measurement http://www.ebi.ac.uk/efo/EFO_0020877 GCST90095458 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Conjugated linoleic acid meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 linoleic acid change measurement http://www.ebi.ac.uk/efo/EFO_0020877 GCST90095459 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Omega-3 fatty acids meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 omega-3 polyunsaturated fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020878 GCST90095460 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Omega-6 fatty acids meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 omega-6 polyunsaturated fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020879 GCST90095461 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Polyunsaturated fatty acids meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 polyunsaturated fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020880 GCST90095462 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Monounsaturated fatty acids (16:1, 18:1) meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095463 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Saturated fatty acids meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095464 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Alanine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 alanine change measurement http://www.ebi.ac.uk/efo/EFO_0020884 GCST90095465 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Glutamine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 glutamine change measurement http://www.ebi.ac.uk/efo/EFO_0020885 GCST90095466 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Isoleucine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 isoleucine change measurement http://www.ebi.ac.uk/efo/EFO_0020887 GCST90095467 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Leucine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 leucine change measurement http://www.ebi.ac.uk/efo/EFO_0020888 GCST90095468 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phenylalanine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 phenylalanine change measurement http://www.ebi.ac.uk/efo/EFO_0020890 GCST90095469 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Acetate meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 acetate change measurement http://www.ebi.ac.uk/efo/EFO_0020892 GCST90095470 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. 3-hydroxybutyrate meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 3-hydroxybutyrate change measurement http://www.ebi.ac.uk/efo/EFO_0020893 GCST90095471 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Creatinine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 creatinine change measurement http://www.ebi.ac.uk/efo/EFO_0020894 GCST90095472 Genome-wide genotyping array 2019-02-12 29750799 Chao MJ 2018-05-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29750799 Population-specific genetic modification of Huntington's disease in Venezuela. Huntington's disease (age at onset) 374 Venezuelan ancestry individuals, 4,061 European ancestry individuals NA Illumina [NR] (imputed) 2 age of onset of Huntington disease http://purl.obolibrary.org/obo/OBA_2001024 GCST007113 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Albumin meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 serum albumin change measurement http://www.ebi.ac.uk/efo/EFO_0020895 GCST90095473 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Histidine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 histidine change measurement http://www.ebi.ac.uk/efo/EFO_0020886 GCST90091819 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin 8,694 African American individuals, 17,400 Hispanic or Latin American individuals, 14,693 European ancestry individuals, 127 Asian ancestry individuals, 20 Native American ancestry individuals, 382 individuals NA Affymetrix, Illumina [21000000] (imputed) 39 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012214 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin 8,694 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 11 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012215 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin 14,693 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 23 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012216 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin 17,400 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 22 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012217 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin concentration 16,353 African American individuals, 20,877 Hispanic or Latin American individuals, 29,587 European ancestry individuals, 635 Asian ancestry individuals, 20 Native American ancestry individuals, 384 individuals NA Affymetrix, Illumina [21000000] (imputed) 18 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012218 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin concentration 16,353 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 6 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012219 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin concentration 29,587 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 6 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012220 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular hemoglobin concentration 20,877 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 9 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012221 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular volume 8,556 African American individuals, 17,141 Hispanic or Latin American individuals, 14,483 European ancestry individuals, 125 Asian ancestry individuals, 594 Native American ancestry individuals, 377 individuals NA Affymetrix, Illumina [21000000] (imputed) 44 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90012222 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular volume 8,556 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 11 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90012223 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular volume 14,483 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 23 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90012224 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Mean corpuscular volume 17,141 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 23 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90012225 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red blood cell count 8,679 African American individuals, 17,412 Hispanic or Latin American individuals, 14,690 European ancestry individuals, 127 Asian ancestry individuals, 20 Native American ancestry individuals, 382 individuals NA Affymetrix, Illumina [21000000] (imputed) 30 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90012226 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red blood cell count 8,679 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 5 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90012227 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red blood cell count 14,690 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 12 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90012228 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red blood cell count 17,412 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 15 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90012229 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red cell distribution width 6,141 African American individuals, 17,272 Hispanic or Latin American individuals, 9,611 European ancestry individuals, 123 Asian ancestry individuals, 20 Native American ancestry individuals, 382 individuals NA Affymetrix, Illumina [21000000] (imputed) 21 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90012230 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red cell distribution width 6,141 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 2 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90012231 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red cell distribution width 9,611 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 8 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90012232 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red blood cell traits (multivariate analysis) 16,802 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 11 erythrocyte count, mean corpuscular hemoglobin concentration, mean corpuscular volume, hematocrit, obsolete_red blood cell distribution width, mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0005192, http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012203 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red blood cell traits (multivariate analysis) 29,513 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 11 erythrocyte count, mean corpuscular hemoglobin concentration, mean corpuscular volume, hematocrit, obsolete_red blood cell distribution width, mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0005192, http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012204 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red blood cell traits (multivariate analysis) 20,697 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 13 erythrocyte count, mean corpuscular hemoglobin concentration, mean corpuscular volume, hematocrit, obsolete_red blood cell distribution width, mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0005192, http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012205 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hematocrit 16,184 African American individuals, 20,704 Hispanic or Latin American individuals, 29,383 European ancestry individuals, 631 Asian ancestry individuals, 601 Native American ancestry individuals, 381 individuals NA Affymetrix, Illumina [21000000] (imputed) 13 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90012206 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hematocrit 16,184 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 1 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90012207 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hematocrit 29,383 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 11 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90012208 Genome-wide genotyping array 2018-09-20 30014611 Weiss RB 2018-07-16 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/30014611 Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in Duchenne muscular dystrophy. Age at loss of ambulation in Duchenne muscular dystrophy 243 European ancestry cases, 10 cases NA Illumina [1735619] 47 Duchenne muscular dystrophy, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0010679, http://www.ebi.ac.uk/efo/EFO_0008336 GCST006286 Genome-wide genotyping array 2018-09-10 30012571 Jia X 2018-07-16 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/30012571 Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population. Childhood steroid-sensitive nephrotic syndrome 224 Japanese ancestry cases, 412 Japanese ancestry controls 216 Japanese ancestry cases, 719 Japanese ancestry controls Affymetrix [4105543] (imputed) 1 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST006246 Genome-wide genotyping array 2018-07-04 29771307 Aponte JL 2018-05-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29771307 Assessment of rosacea symptom severity by genome-wide association study and expression analysis highlights immuno-inflammatory and skin pigmentation genes. Rosacea symptom severity 73,265 European ancestry individuals NA Illumina [at least 950000] (imputed) 98 rosacea severity measurement http://www.ebi.ac.uk/efo/EFO_0009180 GCST005790 Genome-wide genotyping array 2020-02-21 31879980 German CA 2019-12-26 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31879980 Ordered multinomial regression for genetic association analysis of ordinal phenotypes at Biobank scale. Hypertension 30,822 British ancestry normal blood pressure individuals, 25,242 British ancestry elevated blood pressure individuals, 50,461 British ancestry stage 1 hypertension individuals, 75,286 British ancestry stage 2 hypertension individuals, 3,754 British ancestry hypertension crisis individuals NA Affymetrix [464137] 52 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST009685 Genome-wide genotyping array 2020-02-21 31879980 German CA 2019-12-26 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31879980 Ordered multinomial regression for genetic association analysis of ordinal phenotypes at Biobank scale. Airflow obstruction in ever smokers 2,534 European ancestry unaffected individuals, 607 European ancestry stage 1 individuals, 1,424 European ancestry stage 2 individuals, 909 European ancestry stage 3 individuals, 487 European ancestry stage 4 individuals NA NR [630860] 2 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST009684 Genome-wide genotyping array 2020-07-09 32047095 Traglia M 2020-02-11 Genetics www.ncbi.nlm.nih.gov/pubmed/32047095 Genetic Contributions to Maternal and Neonatal Vitamin D Levels. Midgestational total 25-hydroxyvitamin D levels (maternal genetic effect) 269 European ancestry individuals, 323 Hispanic individuals, 115 East Asian ancestry individuals, 23 African American individuals, 23 South Asian ancestry individuals, 23 individuals NA Affymetrix [629686] 3 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST010171 Genome-wide genotyping array 2020-07-09 32047095 Traglia M 2020-02-11 Genetics www.ncbi.nlm.nih.gov/pubmed/32047095 Genetic Contributions to Maternal and Neonatal Vitamin D Levels. Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) 269 European ancestry individuals, 323 Hispanic individuals, 115 East Asian ancestry individuals, 23 African American individuals, 23 South Asian ancestry individuals, 23 individuals NA Affymetrix [629686] 7 vitamin D measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004631, http://www.ebi.ac.uk/efo/EFO_0005939 GCST010170 Genome-wide genotyping array 2020-07-09 32047095 Traglia M 2020-02-11 Genetics www.ncbi.nlm.nih.gov/pubmed/32047095 Genetic Contributions to Maternal and Neonatal Vitamin D Levels. Midgestational total 25-hydroxyvitamin D levels (fetal genetic effect) 269 European ancestry individuals, 323 Hispanic individuals, 115 East Asian ancestry individuals, 23 African American individuals, 23 South Asian ancestry individuals, 23 individuals NA Affymetrix [622716] 3 fetal genotype effect measurement, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0004631 GCST010169 Genome-wide genotyping array 2020-07-09 32047095 Traglia M 2020-02-11 Genetics www.ncbi.nlm.nih.gov/pubmed/32047095 Genetic Contributions to Maternal and Neonatal Vitamin D Levels. Neonatal total 25-hydroxyvitamin D levels (fetal genetic effect) 269 European ancestry individuals, 323 Hispanic individuals, 115 East Asian ancestry individuals, 23 African American individuals, 23 South Asian ancestry individuals, 23 individuals NA Affymetrix [622716] 2 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST010168 Genome-wide genotyping array 2020-07-08 32041948 Sarin KY 2020-02-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32041948 Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma. Cutaneous squamous cell carcinoma 19,149 European ancestry cases, 680,049 European ancestry controls NA NR [13607369] (imputed) 26 cutaneous squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_1001927 GCST010148 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in very large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 3 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091769 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in very large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 2 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091770 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in very large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 2 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091771 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial very large VLDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 2 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091772 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in very large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 2 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091773 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in very large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 2 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091774 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in very small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 9 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091775 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in very small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 8 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091776 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in very small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 8 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091777 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in very small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 11 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091778 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial very small VLDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 8 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091779 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in very small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 9 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091780 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in very small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091781 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in chylomicrons and extremely large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091782 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in chylomicrons and extremely large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 chylomicron measurement, very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091783 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in chylomicrons and extremely large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 3 free cholesterol measurement, chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091784 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in chylomicrons and extremely large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091785 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial chylomicrons and extremely large VLDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091786 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in chylomicrons and extremely large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091787 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in chylomicrons and extremely large VLDL 4,348 individuals NA Illumina [7701709] (imputed) 3 chylomicron measurement, triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091788 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Docosahexaenoic acid (22:6) meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 docosahexaenoic acid change measurement http://www.ebi.ac.uk/efo/EFO_0020876 GCST90091789 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020905 GCST90091790 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Glucose meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 glucose change measurement http://www.ebi.ac.uk/efo/EFO_0020881 GCST90091791 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Histidine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 histidine change measurement http://www.ebi.ac.uk/efo/EFO_0020886 GCST90091792 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in IDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 2 triglyceride change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90091793 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides in LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091794 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in medium LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091795 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in small HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 2 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091796 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in small LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90091797 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in small LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90091798 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in very large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091799 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in very large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90091800 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in very large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90091801 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in very large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90091802 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in chylomicron and extremely large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 chylomicron measurement, very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90091803 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in chylomicron and extremely large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 chylomicron measurement, very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90091804 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in chylomicron and extremely large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 chylomicron measurement, very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90091805 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in chylomicrons and extremely large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 lipid change measurement, chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091806 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Chylomicron and extremely large VLDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 chylomicron change measurement, very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020901, http://www.ebi.ac.uk/efo/EFO_0020857 GCST90091807 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in chylomicrons and extremely large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90091808 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in chylomicrons and extremely large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 1 chylomicron measurement, very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90091809 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in medium HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091810 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in small HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091811 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Citrate meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 citrate change measurement http://www.ebi.ac.uk/efo/EFO_0020883 GCST90091812 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in very large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091813 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in very large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091814 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in very large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091815 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in very large HDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091816 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Glycoprotein acetyls (mainly a1-acid glycoprotein) meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 glycoprotein change measurement http://www.ebi.ac.uk/efo/EFO_0020896 GCST90091817 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Glucose meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 glucose change measurement http://www.ebi.ac.uk/efo/EFO_0020881 GCST90091818 Genome-wide genotyping array 2021-12-16 34841290 Ghodsian N 2021-11-03 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/34841290 Electronic health record-based genome-wide meta-analysis provides insights on the genetic architecture of non-alcoholic fatty liver disease. Nonalcoholic fatty liver disease 8,434 European ancestry cases, 770,180 European ancestry controls NA NR [6787908] (imputed) 9 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90091033 Genome-wide genotyping array 2018-11-12 30009487 Schoeler NE 2018-07-16 Epilepsia www.ncbi.nlm.nih.gov/pubmed/30009487 Genome-wide association study: Exploring the genetic basis for responsiveness to ketogenic dietary therapies for drug-resistant epilepsy. Response to ketogenic dietary therapies in epilepsy 123 responders, 112 non-responders NA Illumina [4819069] (imputed) 1 response to ketogenic diet http://www.ebi.ac.uk/efo/EFO_0009372 GCST006567 Genome-wide genotyping array 2018-07-12 29738550 de Oliveira Otto MC 2018-05-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/29738550 Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium. Circulating odd-numbered chain saturated fatty acid levels (C15:0) 11,494 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 15 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST005869 Genome-wide genotyping array 2018-07-12 29738550 de Oliveira Otto MC 2018-05-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/29738550 Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium. Circulating odd-numbered chain saturated fatty acid levels (C17:0) 6,016 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 15 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST005868 Genome-wide genotyping array 2018-07-12 29738550 de Oliveira Otto MC 2018-05-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/29738550 Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium. Circulating odd-numbered chain saturated fatty acid levels (C15:0+C17:0) 6,016 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 15 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST005866 Genome-wide genotyping array 2018-07-12 29738550 de Oliveira Otto MC 2018-05-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/29738550 Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium. Circulating odd-numbered chain saturated fatty acid levels (C19:0) 1,910 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 15 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST005862 Genome-wide genotyping array 2018-07-12 29738550 de Oliveira Otto MC 2018-05-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/29738550 Genome-wide association meta-analysis of circulating odd-numbered chain saturated fatty acids: Results from the CHARGE Consortium. Circulating odd-numbered chain saturated fatty acid levels (C23:0) 7,582 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 15 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST005861 Genome-wide genotyping array 2018-09-06 29682794 Szekely E 2018-04-22 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29682794 Genetic associations with childhood brain growth, defined in two longitudinal cohorts. Basal ganglia growth 581 European ancestry individuals, 31 African American individuals, 8 Asian American individuals, 15 admixed individuals, 80 other ancestries individuals NA Illumina [at least 653030] 2 basal ganglia growth measurement http://www.ebi.ac.uk/efo/EFO_0009325 GCST006220 Genome-wide genotyping array 2018-09-06 29682794 Szekely E 2018-04-22 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29682794 Genetic associations with childhood brain growth, defined in two longitudinal cohorts. White matter growth 581 European ancestry individuals, 31 African American individuals, 8 Asian American individuals 15 admixed individuals, 80 other ancestries individuals NA Illumina [at least 653030] 5 white matter growth measurement http://www.ebi.ac.uk/efo/EFO_0009335 GCST006221 Genome-wide genotyping array 2018-09-06 29682794 Szekely E 2018-04-22 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29682794 Genetic associations with childhood brain growth, defined in two longitudinal cohorts. Cerebellum growth 581 European ancestry individuals, 31 African American individuals, 8 Asian American individuals, 15 admixed individuals, 80 other ancestries individuals NA Illumina [at least 653030] 4 cerebellum growth measurement http://www.ebi.ac.uk/efo/EFO_0009327 GCST006222 Genome-wide genotyping array 2018-09-06 29682794 Szekely E 2018-04-22 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29682794 Genetic associations with childhood brain growth, defined in two longitudinal cohorts. Cerebral cortical growth 581 European ancestry individuals, 31 African American individuals, 8 Asian American individuals, 15 admixed individuals, 80 other ancestries individuals NA Illumina [at least 653030] 5 cerebral cortex growth measurement http://www.ebi.ac.uk/efo/EFO_0009328 GCST006223 Genome-wide genotyping array 2018-09-06 29682794 Szekely E 2018-04-22 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29682794 Genetic associations with childhood brain growth, defined in two longitudinal cohorts. Right lateral prefrontal cortical growth 581 European ancestry individuals, 31 African American individuals, 8 Asian American individuals, 15 admixed individuals, 80 other ancestries individuals NA Illumina [at least 653030] 8 prefrontal cortex growth measurement http://www.ebi.ac.uk/efo/EFO_0009334 GCST006224 Genome-wide genotyping array 2018-09-19 29748315 Pott J 2018-05-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/29748315 Genetic Regulation of PCSK9 (Proprotein Convertase Subtilisin/Kexin Type 9) Plasma Levels and Its Impact on Atherosclerotic Vascular Disease Phenotypes. Plasma proprotein convertase subtilisin/kexin type 9 levels in stable coronary artery disease 2,022 European ancestry individuals without statin treatment, 1,268 European ancestry individuals with statin treatment NR Affymetrix [9882017] (imputed) 19 PCSK9 protein measurement http://www.ebi.ac.uk/efo/EFO_0006899 GCST006284 Genome-wide genotyping array 2020-11-04 32335043 Park S 2020-04-22 J Acad Nutr Diet www.ncbi.nlm.nih.gov/pubmed/32335043 Alcohol, Carbohydrate, and Calcium Intakes and Smoking Interactions with APOA5 rs662799 and rs2266788 were Associated with Elevated Plasma Triglyceride Concentrations in a Cross-Sectional Study of Korean Adults. Triglyceride levels 21,014 Korean ancestry individuals with TG < 150mg/dL, 7,424 Korean ancestry individuals with TG ≥ 150 mg/dL NA Affymetrix [830000] 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST010729 Genome-wide genotyping array 2018-07-23 29698431 Roosenboom J 2018-04-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/29698431 Mapping genetic variants for cranial vault shape in humans. Maximum cranial length 4,419 European ancestry individuals NA Illumina [at least 567677] (imputed) 22 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST005938 Genome-wide genotyping array 2018-07-23 29698431 Roosenboom J 2018-04-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/29698431 Mapping genetic variants for cranial vault shape in humans. Cephalic index 4,419 European ancestry individuals NA Illumina [at least 567677] (imputed) 14 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST005939 Genome-wide genotyping array 2018-07-23 29698431 Roosenboom J 2018-04-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/29698431 Mapping genetic variants for cranial vault shape in humans. Maximum cranial width 4,419 European ancestry individuals NA Illumina [at least 567677] (imputed) 20 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST005940 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial medium VLDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091720 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in medium VLDL 4,348 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091721 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in medium VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091722 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phosphatidylcholine and other cholines 4,348 individuals NA Illumina [7701709] (imputed) 4 choline measurement, phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010116, http://www.ebi.ac.uk/efo/EFO_0010226 GCST90091723 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phenylalanine 4,348 individuals NA Illumina [7701709] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90091724 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial polyunsaturated fatty acids 4,348 individuals NA Illumina [7701709] (imputed) 7 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST90091725 Genome-wide genotyping array 2022-10-14 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial remnant cholesterol 4,348 individuals NA Illumina [7701709] (imputed) 5 remnant cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010815 GCST90091726 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial serum total cholesterol 4,348 individuals NA Illumina [7701709] (imputed) 8 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90091727 Genome-wide genotyping array 2022-10-14 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial serum total triglycerides 4,348 individuals NA Illumina [7701709] (imputed) 6 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90091728 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial saturated fatty acids 4,348 individuals NA Illumina [7701709] (imputed) 4 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091729 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in small HDL 4,348 individuals NA Illumina [7701709] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091730 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in small HDL 4,348 individuals NA Illumina [7701709] (imputed) 1 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091731 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in small HDL 4,348 individuals NA Illumina [7701709] (imputed) 5 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091732 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in small HDL 4,348 individuals NA Illumina [7701709] (imputed) 2 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091733 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial small HDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091734 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in small HDL 4,348 individuals NA Illumina [7701709] (imputed) 7 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091735 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in small HDL 4,348 individuals NA Illumina [7701709] (imputed) 3 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091736 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in small LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091737 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in small LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091738 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in small LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091739 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in small LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091740 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial small LDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091741 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in small LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091742 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in small LDL 4,348 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091743 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial sphingomyelins 4,348 individuals NA Illumina [7701709] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90091744 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in IDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 phospholipid change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095383 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in IDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 total cholesterol change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095384 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in IDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 esterified cholesterol change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095385 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in IDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 free cholesterol change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095386 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in IDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 triglyceride change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095387 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091745 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial cholesterol esters in small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091746 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial free cholesterol in small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091747 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total lipids in small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091748 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial small VLDL particle concentration 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091749 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial phospholipid levels in small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091750 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial triglycerides levels in small VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091751 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholines 4,348 individuals NA Illumina [7701709] (imputed) 5 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90091752 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total fatty acids 4,348 individuals NA Illumina [7701709] (imputed) 6 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091753 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total phosphoglycerides 4,348 individuals NA Illumina [7701709] (imputed) 4 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90091754 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial tyrosine 4,348 individuals NA Illumina [7701709] (imputed) 3 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90091755 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial estimated degree of unsaturation 4,348 individuals NA Illumina [7701709] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091756 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial valine 4,348 individuals NA Illumina [7701709] (imputed) 3 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90091757 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial total cholesterol in VLDL 4,348 individuals NA Illumina [7701709] (imputed) 4 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091758 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in chylomicron and extremely large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 chylomicron measurement, very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90091820 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Tyrosine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 tyrosine change measurement http://www.ebi.ac.uk/efo/EFO_0020891 GCST90091821 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Lactate meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 lactate change measurement http://www.ebi.ac.uk/efo/EFO_0020882 GCST90091822 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Valine meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 valine change measurement http://www.ebi.ac.uk/efo/EFO_0020889 GCST90091823 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 1 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90091824 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting diacylglycerol 4,734 individuals NA Illumina [7701709] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90095202 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting conjugated linoleic acid 4,734 individuals NA Illumina [7701709] (imputed) 0 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90095203 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting creatinine 4,734 individuals NA Illumina [7701709] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90095204 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting albumin 4,734 individuals NA Illumina [7701709] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90095205 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial diacylglycerol 4,348 individuals NA Illumina [7701709] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90095206 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial glucose 4,348 individuals NA Illumina [7701709] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90095207 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Valine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 valine change measurement http://www.ebi.ac.uk/efo/EFO_0020889 GCST90095333 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phenylalanine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 phenylalanine change measurement http://www.ebi.ac.uk/efo/EFO_0020890 GCST90095334 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Tyrosine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 tyrosine change measurement http://www.ebi.ac.uk/efo/EFO_0020891 GCST90095335 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Acetate meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 acetate change measurement http://www.ebi.ac.uk/efo/EFO_0020892 GCST90095336 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. 3-hydroxybutyrate meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 3-hydroxybutyrate change measurement http://www.ebi.ac.uk/efo/EFO_0020893 GCST90095337 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Creatinine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 creatinine change measurement http://www.ebi.ac.uk/efo/EFO_0020894 GCST90095338 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Albumin meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 serum albumin change measurement http://www.ebi.ac.uk/efo/EFO_0020895 GCST90095339 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Glycoprotein acetyls (mainly a1-acid glycoprotein) meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 glycoprotein change measurement http://www.ebi.ac.uk/efo/EFO_0020896 GCST90095340 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in chylomicrons and extremely large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 chylomicron change measurement, very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020901, http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095341 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in chylomicrons and extremely large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095342 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in chylomicrons and extremely large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095343 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in chylomicron and extremely large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 chylomicron measurement, very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095344 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in chylomicron and extremely large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 chylomicron measurement, very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095345 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in chylomicrons and extremely large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 chylomicron measurement, very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095346 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095347 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in very large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095348 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in very large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095349 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in very large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095350 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in very large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095351 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in very large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095352 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Large VLDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095353 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095354 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095355 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095356 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095357 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095233 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095234 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095235 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095236 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095237 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095238 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Very small VLDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095239 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in very small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095240 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095241 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in very small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095242 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in very small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095243 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in very small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095244 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in very small VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095245 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. IDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 intermediate density lipoprotein change measurement http://www.ebi.ac.uk/efo/EFO_0020906 GCST90095246 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in IDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095247 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in IDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 phospholipid change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095248 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in IDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095249 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in IDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 esterified cholesterol change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095250 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in IDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 free cholesterol change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095251 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Large LDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST90095252 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in large LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095253 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in large LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095254 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in large LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095255 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in large LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095256 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in large LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 free cholesterol change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095257 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides in VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095308 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides in HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095309 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Diacylglycerol meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 diglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0020868 GCST90095310 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total phosphoglycerides meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 glycerophospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0020869 GCST90095311 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phosphatidylcholine and other cholines meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 phosphatidylcholine change measurement, choline change measurement http://www.ebi.ac.uk/efo/EFO_0020871, http://www.ebi.ac.uk/efo/EFO_0020870 GCST90095312 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Sphingomyelins meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 sphingomyelin change measurement http://www.ebi.ac.uk/efo/EFO_0020872 GCST90095313 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholines meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 choline change measurement http://www.ebi.ac.uk/efo/EFO_0020870 GCST90095314 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Apolipoprotein A-I meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 apolipoprotein A 1 change measurement http://www.ebi.ac.uk/efo/EFO_0020873 GCST90095315 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Apolipoprotein B meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 apolipoprotein B change measurement http://www.ebi.ac.uk/efo/EFO_0020874 GCST90095316 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total fatty acids meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095317 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Estimated description of fatty acid chain length (not actual carbon number) meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095318 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Estimated degree of unsaturation meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095319 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Lactate meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 linoleic acid change measurement http://www.ebi.ac.uk/efo/EFO_0020877 GCST90095320 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Conjugated linoleic acid meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 linoleic acid change measurement http://www.ebi.ac.uk/efo/EFO_0020877 GCST90095321 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Omega-3 fatty acids meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 omega-3 polyunsaturated fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020878 GCST90095322 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Omega-6 fatty acids meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 omega-6 polyunsaturated fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020879 GCST90095323 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Polyunsaturated fatty acids meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 polyunsaturated fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020880 GCST90095324 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Monounsaturated fatty acids (16:1, 18:1) meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095325 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Saturated fatty acids meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 fatty acid change measurement http://www.ebi.ac.uk/efo/EFO_0020875 GCST90095326 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Lactate meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lactate change measurement http://www.ebi.ac.uk/efo/EFO_0020882 GCST90095327 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Citrate meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 citrate change measurement http://www.ebi.ac.uk/efo/EFO_0020883 GCST90095328 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Alanine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 alanine change measurement http://www.ebi.ac.uk/efo/EFO_0020884 GCST90095329 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Glutamine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 glutamine change measurement http://www.ebi.ac.uk/efo/EFO_0020885 GCST90095330 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Isoleucine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 isoleucine change measurement http://www.ebi.ac.uk/efo/EFO_0020887 GCST90095331 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Leucine meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 leucine change measurement http://www.ebi.ac.uk/efo/EFO_0020888 GCST90095332 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial lactate 4,348 individuals NA Illumina [7701709] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90095208 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial alanine 4,348 individuals NA Illumina [7701709] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90095209 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial histidine 4,348 individuals NA Illumina [7701709] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90095210 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial acetate 4,348 individuals NA Illumina [7701709] (imputed) 0 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90095211 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial creatinine 4,348 individuals NA Illumina [7701709] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90095212 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Postprandial albumin 4,348 individuals NA Illumina [7701709] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90095213 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Very large VLDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095214 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in very large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095215 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095216 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in very large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095217 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Large VLDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095218 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095219 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095220 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095221 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095222 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095223 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in large VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095224 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Medium VLDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095225 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in medium VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095226 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in medium VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095227 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in medium VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095228 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in medium VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095229 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in medium VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095230 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in medium VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095231 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Small VLDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095232 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095358 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in large VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095359 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Medium VLDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095360 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in medium VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095361 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in medium VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095362 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in medium VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095363 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in medium VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095364 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in medium VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095365 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in medium VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095366 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Small VLDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095367 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095368 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095369 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095370 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095371 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095372 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095373 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020857 GCST90095374 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in very small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90095375 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095376 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in very small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095377 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in very small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095378 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in very small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, free cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020905 GCST90095379 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in very small VLDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 very low density lipoprotein cholesterol measurement, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095380 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. IDL particle concentration meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 intermediate density lipoprotein change measurement http://www.ebi.ac.uk/efo/EFO_0020906 GCST90095381 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in IDL meal response (LMM) 11,410 individuals NA Illumina [7568622] (imputed) 0 lipid change measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90095382 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Medium HDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095283 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in medium HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095284 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in medium HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095285 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in medium HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095286 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in medium HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095287 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in medium HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095288 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in medium HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095289 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Small HDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095290 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in small HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095291 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in small HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095292 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in small HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095293 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in small HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095294 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in small HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095295 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Mean diameter of VLDLD particles meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein particle size change measurement http://www.ebi.ac.uk/efo/EFO_0020907 GCST90095296 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Mean diameter of LDL particles meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein particle size change measurement http://www.ebi.ac.uk/efo/EFO_0020908 GCST90095297 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Mean diameter of HDL particles meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 high density lipoprotein particle size change measurement http://www.ebi.ac.uk/efo/EFO_0020866 GCST90095298 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Serum total cholesterol meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095299 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in VLDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 very low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095300 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Remnant cholesterol meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 remnant cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020867 GCST90095301 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095302 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095303 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in HDL2 meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095304 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in HDL3 meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095305 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Esterified cholesterol meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095306 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Serum total triglycerides meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0007681 GCST90095307 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in large LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095258 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Medium LDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST90095259 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in medium LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095260 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in medium LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095261 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in medium LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007806 GCST90095262 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in medium LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, esterified cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020904 GCST90095263 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in medium LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 free cholesterol change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095264 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Small LDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST90095265 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in small LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095266 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in small LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid change measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020903 GCST90095267 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in small LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 free cholesterol change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095268 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in small LDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90095269 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Very large HDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095270 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in very large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095271 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in very large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095272 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in very large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095273 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in very large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095274 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in very large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095275 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Large HDL particle concentration meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST90095276 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total lipids in large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 lipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020859, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095277 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Phospholipid levels in large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 phospholipid change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020903, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095278 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Total cholesterol in large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 total cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095279 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Cholesterol esters in large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 esterified cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020904, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095280 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Free cholesterol in large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 free cholesterol change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020905, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095281 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Triglycerides levels in large HDL meal response (OrNLSr) 4,292 individuals NA Illumina [7701709] (imputed) 0 triglyceride change measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095282 Genome-wide genotyping array 2018-08-10 26362759 Rothwell S 2015-09-11 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/26362759 Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups. Dermatomyositis or juvenile dermatomyositis 879 European dermatomyositis cases, 15,651 European juvenile dermatomyositis ancestry controls Illumina [90536] 4 dermatomyositis, juvenile dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000398, http://www.ebi.ac.uk/efo/EFO_0000557 GCST006053 Targeted genotyping array [ImmunoChip] 2018-08-10 26362759 Rothwell S 2015-09-11 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/26362759 Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups. Polymyositis 931 European ancestry cases, 15,651 European ancestry controls Illumina [90536] 8 polymyositis http://www.ebi.ac.uk/efo/EFO_0003063 GCST006052 Targeted genotyping array [ImmunoChip] 2018-08-10 26362759 Rothwell S 2015-09-11 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/26362759 Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups. Idiopathic inflammatory myopathy 2,556 European ancestry cases, 15,651 European ancestry controls Illumina [90536] 7 myositis http://www.ebi.ac.uk/efo/EFO_0000783 GCST006051 Targeted genotyping array [ImmunoChip] 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hematocrit 20,704 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 8 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90012209 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hemoglobin concentration 16,186 African American individuals, 20,692 Hispanic or Latin American individuals, 29,379 European ancestry individuals, 630 Asian ancestry individuals, 601 Native American ancestry individuals, 381 individuals NA Affymetrix, Illumina [21000000] (imputed) 20 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012210 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hemoglobin concentration 16,186 African American individuals NA Affymetrix, Illumina [21000000] (imputed) 6 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012211 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hemoglobin concentration 29,379 European ancestry individuals NA Affymetrix, Illumina [21000000] (imputed) 11 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012212 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Hemoglobin concentration 20,692 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 9 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012213 Genome-wide genotyping array 2021-03-22 32171239 Hodonsky CJ 2020-03-14 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32171239 Ancestry-specific associations identified in genome-wide combined-phenotype study of red blood cell traits emphasize benefits of diversity in genomics. Red cell distribution width 17,272 Hispanic or Latin American individuals NA Affymetrix, Illumina [21000000] (imputed) 16 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90012233 Genome-wide genotyping array 2022-01-12 34387878 Kim KY 2021-08-13 Hepatology www.ncbi.nlm.nih.gov/pubmed/34387878 Genome-wide association of individual vulnerability with alcoholic liver disease: A Korean Genome and Epidemiology Study. Alcohol-associated liver disease in light drinkers 1,379 Korean ancestry cases, 13,132 Korean ancestry controls NA Affymetrix [7975321] (imputed) 26 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90091207 Genome-wide genotyping array 2022-01-12 34387878 Kim KY 2021-08-13 Hepatology www.ncbi.nlm.nih.gov/pubmed/34387878 Genome-wide association of individual vulnerability with alcoholic liver disease: A Korean Genome and Epidemiology Study. Alcohol-associated liver disease in heavy drinkers 1,185 Korean ancestry cases, 2,246 Korean ancestry controls NA Affymetrix [7975321] (imputed) 17 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90091208 Genome-wide genotyping array 2022-01-12 34387878 Kim KY 2021-08-13 Hepatology www.ncbi.nlm.nih.gov/pubmed/34387878 Genome-wide association of individual vulnerability with alcoholic liver disease: A Korean Genome and Epidemiology Study. Alcohol-associated liver disease in non drinkers 782 Korean ancestry cases, 18,058 Korean ancestry controls NA Affymetrix [7975321] (imputed) 28 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90091206 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Alcohol consumption (drinks per week) 58,610 Japanese ancestry individuals NA Illumina [6108828] (imputed) 3 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST009800 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Coffee consumption 152,634 Japanese ancestry individuals NA Illumina [6108828] (imputed) 16 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST009801 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Green tea consumption 152,653 Japanese ancestry individuals NA Illumina [6108828] (imputed) 1 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST009802 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Milk consumption 152,965 Japanese ancestry individuals NA Illumina [6108828] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST009803 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Yoghurt consumption 83,150 Japanese ancestry men, 69,757 Japanese ancestry women NA Illumina [6108828] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST009804 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Cheese consumption 152,714 Japanese ancestry individuals NA Illumina [6108828] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST009805 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Natto consumption 152,678 Japanese ancestry individuals NA Illumina [6108828] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST009806 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Tofu consumption 152,943 Japanese ancestry individuals NA Illumina [6108828] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST009807 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Fish intake frequency 153,048 Japanese ancestry individuals NA Illumina [6108828] (imputed) 1 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST009808 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Small whole fish consumption 82,791 Japanese ancestry men, 69,486 Japanese ancestry women NA Illumina [6108828] (imputed) 1 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST009809 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Vegetable consumption 153,001 Japanese ancestry individuals NA Illumina [6108828] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST009810 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Meat consumption 152,857 Japanese ancestry individuals NA Illumina [6108828] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST009811 Genome-wide genotyping array 2020-03-31 31959922 Matoba N 2020-01-20 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31959922 GWAS of 165,084 Japanese individuals identified nine loci associated with dietary habits. Alcohol consumption (drinkers vs non-drinkers) 83,713 Japanese ancestry ever drinkers, 81,371 Japanese ancestry never drinkers NA Illumina [6108828] (imputed) 6 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST009799 Genome-wide genotyping array 2020-04-16 31969989 Oni-Orisan A 2020-01-16 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/31969989 The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. Response to statins (LDL cholesterol percent change) 28,616 European ancestry individuals, 1,205 African ancestry individuals, 2,350 East Asian ancestry individuals, 2,703 Hispanic/Latino individuals NA Affymetrix [13250765] (imputed) 4 response to statin, LDL cholesterol change measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0007804 GCST009821 Genome-wide genotyping array 2020-03-09 31969989 Oni-Orisan A 2020-01-16 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/31969989 The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. Low density lipoprotein cholesterol levels 28,616 European ancestry individuals, 1,205 African ancestry individuals, 2,350 East Asian ancestry individuals, 2,703 Hispanic/Latino individuals NA Affymetrix [13250765] (imputed) 4 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST009757 Genome-wide genotyping array 2020-07-27 31969989 Oni-Orisan A 2020-01-16 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/31969989 The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. Low density lipoprotein cholesterol levels (on statin treatment) 28,616 European ancestry individuals, 1,205 African ancestry individuals, 2,350 East Asian ancestry individuals, 2,703 Hispanic/Latino individuals NA Affymetrix [13250765] (imputed) 8 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST010337 Genome-wide genotyping array 2020-07-27 31969989 Oni-Orisan A 2020-01-16 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/31969989 The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change. Response to statins (LDL cholesterol change) 28,616 European ancestry individuals, 1,205 African ancestry individuals, 2,350 East Asian ancestry individuals, 2,703 Hispanic/Latino individuals NA Affymetrix [13250765] (imputed) 6 response to statin, LDL cholesterol change measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0007804 GCST010338 Genome-wide genotyping array 2018-07-19 29782485 Rueger S 2018-05-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29782485 Evaluation and application of summary statistic imputation to discover new height-associated loci. Height 253,288 European ancestry individuals 336,474 European ancestry individuals NR [9276018] (imputed) 41 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST005908 Genome-wide genotyping array 2020-03-30 31998841 Thompson A 2020-01-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31998841 Functional validity, role, and implications of heavy alcohol consumption genetic loci. Alcohol consumption (heavy vs. light/non-drinkers) 21,967 British ancestry cases, 103,282 British ancestry controls 47,967 European ancestry individuals Affymetrix [11141077] (imputed) 10 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST009797 Genome-wide genotyping array 2021-04-29 32048322 Kim Y 2020-02-11 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32048322 Genome-wide interaction study of single-nucleotide polymorphisms and alcohol consumption on blood pressure: The Ansan and Ansung study of the Korean Genome and Epidemiology Study (KoGES). Blood pressure x alcohol consumption interaction 6,176 Korean ancestry individuals 18,708 Korean ancestry individuals Affymetrix [5908513] (imputed) 0 diastolic blood pressure, systolic blood pressure, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0007878 GCST011571 Genome-wide genotyping array 2021-12-20 32139696 Shu X 2020-03-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32139696 Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants. Breast cancer 24,206 East Asian ancestry cases, 24,775 East Asian ancestry controls, 122,977 European ancestry cases, 105,974 European ancestry controls 10,829 East Asian ancestry cases, 10,996 East Asian ancestry controls, 5,958 Asian ancestry cases, 5,684 Asian ancestry controls Affymetrix, Illumina [NR] (imputed) 151 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90090980 Genome-wide genotyping array 2021-12-20 32139696 Shu X 2020-03-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32139696 Identification of novel breast cancer susceptibility loci in meta-analyses conducted among Asian and European descendants. Breast cancer 35,035 East Asian ancestry cases, 35,771 East Asian ancestry controls, 5,958 Asian ancestry cases, 5,684 Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 8 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90091211 Genome-wide genotyping array 2020-09-01 30226566 Yamada Y 2018-09-04 Int J Mol Med www.ncbi.nlm.nih.gov/pubmed/30226566 Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease. Myocardial infarction 1,152 Japanese ancestry cases, 5,774 Japanese ancestry controls NA Illumina [31245] 21 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST010476 Exome genotyping array 2020-09-01 30226566 Yamada Y 2018-09-04 Int J Mol Med www.ncbi.nlm.nih.gov/pubmed/30226566 Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease. Chronic kidney disease 1,051 Japanese ancestry cases, 1,505 Japanese ancestry controls NA Illumina [31514] 11 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST010478 Exome genotyping array 2020-09-01 30226566 Yamada Y 2018-09-04 Int J Mol Med www.ncbi.nlm.nih.gov/pubmed/30226566 Identification of 13 novel susceptibility loci for early-onset myocardial infarction, hypertension, or chronic kidney disease. Hypertension 3,444 Japanese ancestry cases, 4,636 Japanese ancestry controls NA Illumina [31276] 10 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST010477 Exome genotyping array [Exome array] 2018-06-26 29784950 Sawai H 2018-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29784950 Genome-wide association study identified new susceptible genetic variants in HLA class I region for hepatitis B virus-related hepatocellular carcinoma. Hepatocellular carcinoma in hepatitis B infection 473 Japanese ancestry chronic hepatitis and hepatocellular carcinoma cases, 516 Japanese ancestry asymptomatic carriers or chronic hepatitis cases without hepatocellular carcinoma 153 Japanese ancestry chronic hepatitis and hepatocellular carcinoma cases, 614 Japanese ancestry asymptomatic carriers or chronic hepatitis cases without hepatocellular carcinoma, 94 Chinese ancestry chronic hepatitis and hepatocellular carcinoma cases, 187 Chinese ancestry asymptomatic carriers or chronic hepatitis cases without hepatocellular carcinoma, 185 Thai ancestry chronic hepatitis and hepatocellular carcinoma cases, 198 Thai ancestry asymptomatic carriers or chronic hepatitis cases without hepatocellular carcinoma Affymetrix [447830] 7 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST005746 Genome-wide genotyping array 2019-03-27 29786918 Vonk JM 2018-05-22 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/29786918 Novel genes and insights in complete asthma remission. Clinical remission in asthma 178 European ancestry remitted asthma cases, 612 European ancestry persistent asthma controls 135 European ancestry remitted asthma cases, 321 European ancestry persistent asthma controls Illumina [156954] 0 remission http://www.ebi.ac.uk/efo/EFO_0009785 GCST007423 Genome-wide genotyping array 2019-03-27 29786918 Vonk JM 2018-05-22 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/29786918 Novel genes and insights in complete asthma remission. Complete remission in asthma 55 European ancestry remitted asthma cases, 612 European ancestry persistent asthma controls 21 European ancestry remitted asthma cases, 321 European ancestry persistent asthma controls Illumina [156954] 1 remission http://www.ebi.ac.uk/efo/EFO_0009785 GCST007424 Genome-wide genotyping array 2018-07-20 29743610 Ostrom QT 2018-05-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29743610 Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. Glioma 4,831 European ancestry male cases, 3,206 European ancestry female cases, 5,216 European ancestry male controls, 5,470 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 17 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST005931 Genome-wide genotyping array 2018-07-20 29743610 Ostrom QT 2018-05-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29743610 Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. Glioblastoma 2,835 European ancestry male cases, 1,682 European ancestry female cases, 5,216 European ancestry male controls, 5,470 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 14 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST005932 Genome-wide genotyping array 2018-07-20 29743610 Ostrom QT 2018-05-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29743610 Sex-specific glioma genome-wide association study identifies new risk locus at 3p21.31 in females, and finds sex-differences in risk at 8q24.21. Non-glioblastoma glioma 1,716 European ancestry male cases, 1,320 European ancestry female cases, 5,216 European ancestry male controls, 5,470 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 11 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST005933 Genome-wide genotyping array 2018-12-18 29670602 Moreau K 2018-04-04 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/29670602 Human Genetic Susceptibility to Native Valve Staphylococcus aureus Endocarditis in Patients With S. aureus Bacteremia: Genome-Wide Association Study. Infective endocarditis in Staphylococcus aureus infection 67 European ancestry cases, 72 European ancestry controls 57 Danish ancestry cases, 123 Danish ancestry controls Illumina [631710] 0 bacterial endocarditis http://www.ebi.ac.uk/efo/EFO_1000830 GCST006805 Genome-wide genotyping array 2018-08-14 29892016 Schumacher FR 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892016 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Prostate cancer aggressiveness (high vs low) 15,561 European ancestry high aggressive cases, 9,739 European ancestry low aggressive cases NA Illumina [20370935] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST006080 Genome-wide genotyping array 2018-08-14 29892016 Schumacher FR 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892016 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Prostate cancer aggressiveness (high vs low/intermediate) 20,658 European ancestry high aggressive cases, 38,093 European ancestry low/intermediate aggressive cases NA Illumina [20370935] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST006082 Genome-wide genotyping array 2018-08-14 29892016 Schumacher FR 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892016 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Prostate cancer (advanced vs non-advanced) 14,160 European ancestry advanced cases, 62,421 European ancestry non-advanced cases NA Illumina [20370935] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST006081 Genome-wide genotyping array 2018-08-14 29892016 Schumacher FR 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892016 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Prostate cancer (advanced) 15,167 European ancestry cases, 58,308 European ancestry controls NA Illumina [20370935] (imputed) 18 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST006083 Genome-wide genotyping array 2018-08-14 29892016 Schumacher FR 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892016 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Prostate cancer (early onset) 6,988 European ancestry cases, 44,256 European ancestry controls NA Illumina [20370935] (imputed) 11 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST006089 Genome-wide genotyping array 2018-08-14 29892016 Schumacher FR 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892016 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Prostate cancer (Gleason score) 61,978 European ancestry cases NA Illumina [20370935] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST006084 Genome-wide genotyping array 2018-08-14 29892016 Schumacher FR 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892016 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Prostate cancer 79,148 European ancestry cases, 61,106 European ancestry controls NA Illumina [20370935] (imputed) 140 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST006085 Genome-wide genotyping array 2018-08-03 29767774 Lutz SM 2018-05-15 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/29767774 Common and rare variants genetic association analysis of cigarettes per day among ever smokers in COPD cases and controls. Current cigarettes per day in chronic obstructive pulmonary disease 2,812 European ancestry cases, 3,846 European ancestry controls, 821 African American cases, 2,459 African American controls 2,627 cases, 986 controls Illumina [NR] 2 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST006042 Genome-wide genotyping array 2019-03-13 30664634 Rask-Andersen M 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664634 Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. Body fat distribution (arm fat ratio) 55,006 British ancestry males, 61,132 British ancestry females 112,425 British ancestry males, 133,936 British ancestry females Affymetrix [25472837] (imputed) 144 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST007293 Genome-wide genotyping array 2019-03-13 30664634 Rask-Andersen M 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664634 Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. Body fat distribution (leg fat ratio) 55,006 British ancestry males, 61,132 British ancestry females 112,425 British ancestry males, 133,936 British ancestry females Affymetrix [25472837] (imputed) 176 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST007295 Genome-wide genotyping array 2019-03-13 30664634 Rask-Andersen M 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664634 Genome-wide association study of body fat distribution identifies adiposity loci and sex-specific genetic effects. Body fat distribution (trunk fat ratio) 55,006 British ancestry males, 61,132 British ancestry females 112,425 British ancestry males, 133,936 British ancestry females Affymetrix [25472837] (imputed) 186 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST007294 Genome-wide genotyping array 2020-09-20 32887874 Saw J 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887874 Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. Spontaneous coronary artery dissection up to 243 European ancestry cases, up to 23 East Asian ancestry cases, up to 4,816 European ancestry controls, up to 447 East Asian ancestry controls up to 149 European ancestry cases, up to 14 East Asian ancestry cases, up to 2,935 European ancestry controls, up to 272 East Asian ancestry controls Illumina [6690240] (imputed) 17 spontaneous coronary artery dissection http://www.ebi.ac.uk/efo/EFO_0010820 GCST90000582 Genome-wide genotyping array 2020-09-20 32887874 Saw J 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887874 Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction. Spontaneous coronary artery dissection up to 221 European ancestry female cases, up to 20 East Asian ancestry female cases, up to 4,258 European ancestry female controls, up to 395 East Asian ancestry female controls up to 134 European ancestry female cases, up to 12 East Asian ancestry female cases, up to 2,608 European ancestry female controls, up to 242 East Asian female controls Illumina [6690240] (imputed) 4 spontaneous coronary artery dissection http://www.ebi.ac.uk/efo/EFO_0010820 GCST90000583 Genome-wide genotyping array 2018-09-06 29967566 Roberts CH 2018-06-03 Mediators Inflamm www.ncbi.nlm.nih.gov/pubmed/29967566 Pathway-Wide Genetic Risks in Chlamydial Infections Overlap between Tissue Tropisms: A Genome-Wide Association Scan. Anti-chlamydia trachomatis IgG seropositivity 71 Dutch ancestry cases, 169 Dutch ancestry controls NA Illumina [9443221] (imputed) 5 Chlamydia trachomatis seropositivity http://www.ebi.ac.uk/efo/EFO_0009330 GCST006225 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in small HDL 4,734 individuals NA Illumina [7701709] (imputed) 5 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091595 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in small HDL 4,734 individuals NA Illumina [7701709] (imputed) 5 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091596 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in small LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091597 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in small LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091598 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in small LDL 4,734 individuals NA Illumina [7701709] (imputed) 8 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091599 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in small LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091600 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting small LDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091601 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in small LDL 4,734 individuals NA Illumina [7701709] (imputed) 8 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091602 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in small LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091603 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting sphingomyelins 4,734 individuals NA Illumina [7701709] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90091604 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 6 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091605 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 7 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091606 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 6 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091607 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 6 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091608 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting small VLDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091609 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 6 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091610 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in small VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091611 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholines 4,734 individuals NA Illumina [7701709] (imputed) 4 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90091612 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total fatty acids 4,734 individuals NA Illumina [7701709] (imputed) 7 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091613 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total phosphoglycerides 4,734 individuals NA Illumina [7701709] (imputed) 6 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90091614 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting tyrosine 4,734 individuals NA Illumina [7701709] (imputed) 4 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90091615 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting estimated degree of unsaturation 4,734 individuals NA Illumina [7701709] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091616 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting valine 4,734 individuals NA Illumina [7701709] (imputed) 2 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90091617 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091618 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting mean diameter of VLDLD particles 4,734 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90091619 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in medium LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091570 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in medium LDL 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091571 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting medium LDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90091572 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in medium LDL 4,734 individuals NA Illumina [7701709] (imputed) 8 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091573 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in medium LDL 4,734 individuals NA Illumina [7701709] (imputed) 6 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST90091574 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting monounsaturated fatty acids (16:1, 18:1) 4,734 individuals NA Illumina [7701709] (imputed) 6 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091575 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in medium VLDL 4,734 individuals NA Illumina [7701709] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091576 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in medium VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90091577 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in medium VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091578 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in medium VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90091579 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting medium VLDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091580 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phospholipid levels in medium VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90091581 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting triglycerides levels in medium VLDL 4,734 individuals NA Illumina [7701709] (imputed) 5 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90091582 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phosphatidylcholine and other cholines 4,734 individuals NA Illumina [7701709] (imputed) 4 choline measurement, phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010116, http://www.ebi.ac.uk/efo/EFO_0010226 GCST90091583 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting phenylalanine 4,734 individuals NA Illumina [7701709] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90091584 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting polyunsaturated fatty acids 4,734 individuals NA Illumina [7701709] (imputed) 6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST90091585 Genome-wide genotyping array 2022-10-14 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting remnant cholesterol 4,734 individuals NA Illumina [7701709] (imputed) 7 remnant cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010815 GCST90091586 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting serum total cholesterol 4,734 individuals NA Illumina [7701709] (imputed) 8 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90091587 Genome-wide genotyping array 2022-10-14 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting serum total triglycerides 4,734 individuals NA Illumina [7701709] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90091588 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting saturated fatty acids 4,734 individuals NA Illumina [7701709] (imputed) 5 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90091589 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total cholesterol in small HDL 4,734 individuals NA Illumina [7701709] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091590 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting cholesterol esters in small HDL 4,734 individuals NA Illumina [7701709] (imputed) 1 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091591 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting free cholesterol in small HDL 4,734 individuals NA Illumina [7701709] (imputed) 2 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091592 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting total lipids in small HDL 4,734 individuals NA Illumina [7701709] (imputed) 1 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091593 Genome-wide genotyping array 2022-03-22 34610981 Li-Gao R 2021-10-05 Diabetes www.ncbi.nlm.nih.gov/pubmed/34610981 Genetic Studies of Metabolomics Change After a Liquid Meal Illuminate Novel Pathways for Glucose and Lipid Metabolism. Fasting small HDL particle concentration 4,734 individuals NA Illumina [7701709] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90091594 Genome-wide genotyping array 2020-02-19 31757997 Low SK 2019-11-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31757997 Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population. Breast cancer 6,669 Japanese ancestry cases, 21,930 Japanese ancestry controls 981 Japanese ancestry cases, 1,394 Japanese ancestry controls Illumina [4946503] (imputed) 25 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST009665 Genome-wide genotyping array 2018-09-19 29739359 Graham PS 2018-05-08 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/29739359 Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy. Diabetic macular edema in type 2 diabetes 270 European ancestry cases, 435 European ancestry controls NA Illumina [617130] 2 diabetic macular edema http://www.ebi.ac.uk/efo/EFO_0009321 GCST006282 Genome-wide genotyping array 2018-09-19 29739359 Graham PS 2018-05-08 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/29739359 Genome-wide association studies for diabetic macular edema and proliferative diabetic retinopathy. Proliferative diabetic retinopathy in type 2 diabetes 176 European ancestry cases, 435 European ancestry controls NA Illumina [617130] 2 proliferative diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0009322 GCST006283 Genome-wide genotyping array 2019-11-18 31420334 Lindstrom S 2019-08-16 Blood www.ncbi.nlm.nih.gov/pubmed/31420334 Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. Venous thromboembolism 29,435 European ancestry cases, 157,769 European ancestry controls NA Affymetrix, Illumina [12923718] (imputed) 109 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST009029 Genome-wide genotyping array, Exome-wide sequencing 2019-11-18 31420334 Lindstrom S 2019-08-16 Blood www.ncbi.nlm.nih.gov/pubmed/31420334 Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. Venous thromboembolism 799 African American cases, 14,353 African American controls NA Affymetrix, Illumina [12923718] (imputed) 12 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST009031 Genome-wide genotyping array 2019-11-18 31420334 Lindstrom S 2019-08-16 Blood www.ncbi.nlm.nih.gov/pubmed/31420334 Genomic and Transcriptomic Association Studies Identify 16 Novel Susceptibility Loci for Venous Thromboembolism. Venous thromboembolism 29,435 European ancestry cases, 799 African American cases, 157,769 European ancestry controls, 14,353 African American controls NA Affymetrix, Illumina [12923718] (imputed) 34 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST009030 Genome-wide genotyping array, Exome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Red cell distribution width up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 2 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST009032 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Hematocrit up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST009033 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Hemoglobin levels up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST009034 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Mean platelet volume up to 6,407 African ancestry individuals NA Affymetrix, Illumina [at least 20594556] (imputed) 1 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST009035 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Platelet count up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST009036 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Lymphocyte count up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST009037 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Monocyte count up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST009038 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Basophil count up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST009039 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Neutrophil count up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 2 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST009040 Genome-wide genotyping array, Genome-wide sequencing 2020-02-17 31767839 Vijayakrishnan J 2019-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31767839 Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. B-cell acute lymphoblastic leukaemia 5,321 European ancestry cases, 16,666 European ancestry controls 2,237 cases, 3,461 controls Affymetrix, Illumina [~ 6118121] (imputed) 10 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST009638 Genome-wide genotyping array 2020-02-17 31767839 Vijayakrishnan J 2019-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31767839 Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. B-cell acute lymphoblastic leukaemia (high-hyperdiploidy) 1,369 European ancestry cases, 16,666 European ancestry controls 422 cases, 3,461 controls Affymetrix, Illumina [~ 6118121] (imputed) 1 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST009637 Genome-wide genotyping array 2020-02-17 31767839 Vijayakrishnan J 2019-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31767839 Identification of four novel associations for B-cell acute lymphoblastic leukaemia risk. B-cell acute lymphoblastic leukaemia (ETV6-RUNX1 positive) 936 European ancestry cases, 16,666 European ancestry controls 365 cases, 3,461 controls Affymetrix, Illumina [~ 6118121] (imputed) 1 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST009636 Genome-wide genotyping array 2020-07-21 32341051 Wang X 2020-04-01 BMJ Open Diabetes Res Care www.ncbi.nlm.nih.gov/pubmed/32341051 Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis. Circulating leptin levels or fasting insulin levels 254,263 individuals NA NR [NR] 1 leptin measurement, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0005000, http://www.ebi.ac.uk/efo/EFO_0004466 GCST010271 Genome-wide genotyping array 2020-07-21 32341051 Wang X 2020-04-01 BMJ Open Diabetes Res Care www.ncbi.nlm.nih.gov/pubmed/32341051 Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis. Circulating leptin levels or HOMA-B 254,263 individuals NA NR [NR] 1 leptin measurement, HOMA-B http://www.ebi.ac.uk/efo/EFO_0005000, http://www.ebi.ac.uk/efo/EFO_0004469 GCST010270 Genome-wide genotyping array 2020-07-21 32341051 Wang X 2020-04-01 BMJ Open Diabetes Res Care www.ncbi.nlm.nih.gov/pubmed/32341051 Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis. Circulating leptin levels or HOMA-IR 254,263 individuals NA NR [NR] 1 leptin measurement, HOMA-IR http://www.ebi.ac.uk/efo/EFO_0005000, http://www.ebi.ac.uk/efo/EFO_0004501 GCST010269 Genome-wide genotyping array 2020-07-21 32341051 Wang X 2020-04-01 BMJ Open Diabetes Res Care www.ncbi.nlm.nih.gov/pubmed/32341051 Shared genetic architecture and casual relationship between leptin levels and type 2 diabetes: large-scale cross-trait meta-analysis and Mendelian randomization analysis. Circulating leptin levels or type 2 diabetes 254,263 individuals NA NR [NR] 12 leptin measurement, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0005000, http://purl.obolibrary.org/obo/MONDO_0005148 GCST010272 Genome-wide genotyping array 2020-02-18 31779001 Franck M 2019-11-28 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/31779001 Prevention of Potential Adverse Metabolic Effects of a Supplementation with Omega-3 Fatty Acids Using a Genetic Score Approach. Impaired insulin sensitivity in response to n-3 PUFA supplementation 32 French Canadian ancestry cases, 106 French Canadian ancestry controls NA Illumina [2668805] 8 insulin sensitivity measurement, response to polyunsaturated fatty acid supplementation http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0009131 GCST009642 Genome-wide genotyping array 2020-05-22 32266149 He Y 2020-03-20 Front Oncol www.ncbi.nlm.nih.gov/pubmed/32266149 Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma. Head and neck squamous cell carcinoma 261 Chinese ancestry cases 525 Chinese ancestry cases Illumina [247870] 2 head and neck squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000181 GCST009985 Exome genotyping array [Exome array] 2021-06-04 32989782 Goddard PC 2020-09-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32989782 Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function. Lung function (FVC) in asthma 104 African American individuals NA Affymetrix [15954804] (imputed) 17 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST011796 Genome-wide genotyping array 2021-06-04 32989782 Goddard PC 2020-09-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32989782 Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function. Lung function (FEV1/FVC) in asthma 96 African American individuals NA Affymetrix [15954804] (imputed) 22 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST011797 Genome-wide genotyping array 2021-06-04 32989782 Goddard PC 2020-09-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32989782 Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function. Post-bronchodilator lung function in asthma (FEV1) 107 African American individuals NA Affymetrix [15954804] (imputed) 8 forced expiratory volume, response to bronchodilator http://www.ebi.ac.uk/efo/EFO_0004314, http://purl.obolibrary.org/obo/GO_0097366 GCST011799 Genome-wide genotyping array 2021-06-04 32989782 Goddard PC 2020-09-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32989782 Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function. Post-bronchodilator lung function in asthma (FVC) 109 African American individuals NA Affymetrix [15954804] (imputed) 14 response to bronchodilator, vital capacity http://purl.obolibrary.org/obo/GO_0097366, http://www.ebi.ac.uk/efo/EFO_0004312 GCST011800 Genome-wide genotyping array 2021-06-04 32989782 Goddard PC 2020-09-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32989782 Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function. Post-bronchodilator lung function in asthma (FEV1/FVC) 99 African American individuals NA Affymetrix [15954804] (imputed) 21 response to bronchodilator, FEV/FEC ratio http://purl.obolibrary.org/obo/GO_0097366, http://www.ebi.ac.uk/efo/EFO_0004713 GCST011801 Genome-wide genotyping array 2021-06-04 32989782 Goddard PC 2020-09-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32989782 Integrative genomic analysis in African American children with asthma finds three novel loci associated with lung function. Lung function (FEV1) in asthma 99 African American individuals NA Affymetrix [15954804] (imputed) 11 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST011798 Genome-wide genotyping array 2020-06-16 32313116 Manry J 2020-04-20 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32313116 Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway. Buruli ulcer 402 Sub-Saharan African ancestry cases, 401 Sub-Saharan African ancestry controls 455 Sub-Saharan African ancestry cases, 238 Sub-Saharan African ancestry controls Illumina [10014109] (imputed) 1 Buruli ulcer disease http://purl.obolibrary.org/obo/MONDO_0000327 GCST010077 Genome-wide genotyping array 2020-06-16 32313116 Manry J 2020-04-20 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32313116 Genome-wide association study of Buruli ulcer in rural Benin highlights role of two LncRNAs and the autophagy pathway. Buruli ulcer (age at onset) 402 Sub-Saharan African ancestry cases 455 Sub-Saharan African ancestry cases Illumina [10014109] (imputed) 1 age of onset of Buruli ulcer disease http://purl.obolibrary.org/obo/OBA_2001020 GCST010076 Genome-wide genotyping array 2020-05-12 32281736 Fan R 2020-04-13 Addict Biol www.ncbi.nlm.nih.gov/pubmed/32281736 Gene-based association analysis reveals involvement of LAMA5 and cell adhesion pathways in nicotine dependence in African- and European-American samples. Nicotine dependence 1,644 African American cases, 1,727 African American controls 852 Europen ancestry cases, 720 European ancestry controls Illumina [up to 111643] 1 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST009957 Exome genotyping array [Exome array] 2020-07-27 32341457 Sato Y 2020-04-27 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32341457 Genome-wide association study of semen volume, sperm concentration, testis size, and plasma inhibin B levels. Inhibin B levels 811 Japanese ancestry individuals 721 Japanese ancestry individuals Illumina [3901256] (imputed) 1 Inhibin B measurement http://www.ebi.ac.uk/efo/EFO_0010746 GCST010336 Genome-wide genotyping array 2020-07-23 32341457 Sato Y 2020-04-27 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32341457 Genome-wide association study of semen volume, sperm concentration, testis size, and plasma inhibin B levels. Semen volume 811 Japanese ancestry individuals 721 Japanese ancestry individuals Illumina [3901256] (imputed) 0 semen measurement http://www.ebi.ac.uk/efo/EFO_0010745 GCST010310 Genome-wide genotyping array 2020-07-23 32341457 Sato Y 2020-04-27 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32341457 Genome-wide association study of semen volume, sperm concentration, testis size, and plasma inhibin B levels. Sperm concentration 811 Japanese ancestry individuals 721 Japanese ancestry individuals Illumina [3901256] (imputed) 0 sperm measurement http://www.ebi.ac.uk/efo/EFO_0010743 GCST010309 Genome-wide genotyping array 2020-07-23 32341457 Sato Y 2020-04-27 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32341457 Genome-wide association study of semen volume, sperm concentration, testis size, and plasma inhibin B levels. Testis size 811 Japanese ancestry individuals 721 Japanese ancestry individuals Illumina [3901256] (imputed) 0 testis size http://www.ebi.ac.uk/efo/EFO_0010744 GCST010308 Genome-wide genotyping array 2020-09-29 31985003 Boocock J 2020-01-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31985003 Genomic dissection of 43 serum urate-associated loci provides multiple insights into molecular mechanisms of urate control. Urate levels 110,238 European ancestry individuals, 21,471 East Asian individuals NA NR [NR] (imputed) 33 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST010637 Genome-wide genotyping array 2020-01-28 31930058 Niu LD 2019-11-01 Ann Transl Med www.ncbi.nlm.nih.gov/pubmed/31930058 Genome-wide association study of cerebrospinal fluid neurofilament light levels in non-demented elders. Cerebrospinal fluid neurofilament light levels 263 European ancestry individuals NA Illumina [441611] 3 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST009517 Genome-wide genotyping array 2019-08-29 31315583 Lona-Durazo F 2019-07-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/31315583 Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. Skin pigmentation (conditioned on rs1426654 and rs35397) 1,047 Hispanic/Latin American individuals, 684 Cape Verdian individuals, 373 African American individuals NA Affymetrix, Illumina [at least 292549] (imputed) 79 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST008516 Genome-wide genotyping array 2019-08-29 31315583 Lona-Durazo F 2019-07-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/31315583 Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. Skin pigmentation 762 Cuban ancestry individuals NA NR [292549] (imputed) 54 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST008518 Genome-wide genotyping array 2019-08-29 31315583 Lona-Durazo F 2019-07-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/31315583 Meta-analysis of GWA studies provides new insights on the genetic architecture of skin pigmentation in recently admixed populations. Skin pigmentation 1,047 Hispanic/Latin American individuals, 684 Cape Verdian individuals, 373 African American individuals East African ancestry individuals (See Crawford et. al, 2017) Affymetrix, Illumina [at least 292549] (imputed) 7 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST008519 Genome-wide genotyping array 2019-07-09 30662464 Yang C 2018-12-18 J Oncol www.ncbi.nlm.nih.gov/pubmed/30662464 Clinical Implication and the Hereditary Factors of NM23 in Hepatocellular Carcinoma Based on Bioinformatics Analysis and Genome-Wide Association Study. Nucleoside diphosphate kinase A levels in hepatocellular carcinoma 408 East Asian ancestry individuals NA Illumina [21529] 0 nucleoside diphosphate kinase A measurement http://www.ebi.ac.uk/efo/EFO_0009947 GCST008104 Genome-wide genotyping array 2020-01-29 31707593 Kulminski AM 2019-11-09 Geroscience www.ncbi.nlm.nih.gov/pubmed/31707593 Polygenic risk score for disability and insights into disability-related molecular mechanisms. Disability (impaired activities of daily living) 7,544 European ancestry cases, 4,619 European ancestry controls 5,006 European ancestry cases, 6,899 European ancestry controls Illumina [NR] 4 activities of daily living score measurement http://www.ebi.ac.uk/efo/EFO_0008451 GCST009526 Genome-wide genotyping array 2020-02-14 31776335 Jonsson BA 2019-11-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31776335 Brain age prediction using deep learning uncovers associated sequence variants. Brain age (difference between predicted and chronological age) 12,378 British ancestry individuals 4,456 British ancestry individuals Affymetrix [20000000] (imputed) 0 brain age measurement http://www.ebi.ac.uk/efo/EFO_0010602 GCST009611 Genome-wide genotyping array 2020-02-07 31761296 Hernandez Cordero AI 2019-11-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31761296 Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2. Appendicular lean mass 85,750 European ancestry middle-aged adult individuals NA Affymetrix [21375087] (imputed) 182 appendicular lean mass http://www.ebi.ac.uk/efo/EFO_0004980 GCST009576 Genome-wide genotyping array 2020-02-07 31761296 Hernandez Cordero AI 2019-11-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31761296 Genome-wide Associations Reveal Human-Mouse Genetic Convergence and Modifiers of Myogenesis, CPNE1 and STC2. Appendicular lean mass 181,862 European ancestry elderly individuals NA Affymetrix [17914406] (imputed) 391 appendicular lean mass http://www.ebi.ac.uk/efo/EFO_0004980 GCST009577 Genome-wide genotyping array 2020-02-17 31834638 Gloaguen E 2019-12-13 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/31834638 General regression model: A "model-free" association test for quantitative traits allowing to test for the underlying genetic model. Hemoglobin A1c levels 695 individuals NA Illumina [301183] 2 hemoglobin A1 measurement http://www.ebi.ac.uk/efo/EFO_0007629 GCST009641 Genome-wide genotyping array 2020-02-19 31636452 Satizabal CL 2019-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31636452 Genetic architecture of subcortical brain structures in 38,851 individuals. Nucleus accumbens volume 32,562 European ancestry individuals 341 South East and East Asian ancestry individuals, 85 African American individuals Affymetrix, Illumina [NR] (imputed) 9 nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006931 GCST009670 Genome-wide genotyping array 2020-02-19 31636452 Satizabal CL 2019-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31636452 Genetic architecture of subcortical brain structures in 38,851 individuals. Amygdala volume 34,431 European ancestry individuals 341 South East and East Asian ancestry individuals, 769 African American individuals Affymetrix, Illumina [NR] (imputed) 1 amygdala volume http://www.ebi.ac.uk/efo/EFO_0006934 GCST009664 Genome-wide genotyping array 2020-02-25 31636452 Satizabal CL 2019-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31636452 Genetic architecture of subcortical brain structures in 38,851 individuals. Brainstem volume 28,809 European ancestry individuals 341 South East and East Asian ancestry individuals, 85 African American individuals Affymetrix, Illumina [NR] (imputed) 17 brain stem volume measurement http://www.ebi.ac.uk/efo/EFO_0010605 GCST009697 Genome-wide genotyping array 2020-02-19 31636452 Satizabal CL 2019-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31636452 Genetic architecture of subcortical brain structures in 38,851 individuals. Caudate nucleus volume 37,741 European ancestry individuals 341 South East and East Asian ancestry individuals, 769 African American individuals Affymetrix, Illumina [NR] (imputed) 17 caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0004830 GCST009666 Genome-wide genotyping array 2020-02-19 31636452 Satizabal CL 2019-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31636452 Genetic architecture of subcortical brain structures in 38,851 individuals. Pallidum volume 34,413 European ancestry individuals 341 South East and East Asian ancestry individuals, 769 African American individuals Affymetrix, Illumina [NR] (imputed) 11 pallidum volume http://www.ebi.ac.uk/efo/EFO_0006933 GCST009667 Genome-wide genotyping array 2020-02-19 31636452 Satizabal CL 2019-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31636452 Genetic architecture of subcortical brain structures in 38,851 individuals. Putamen volume 37,571 European ancestry individuals 341 South East and East Asian ancestry individuals, 769 African American individuals Affymetrix, Illumina [NR] (imputed) 16 putamen volume http://www.ebi.ac.uk/efo/EFO_0006932 GCST009668 Genome-wide genotyping array 2020-02-19 31636452 Satizabal CL 2019-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31636452 Genetic architecture of subcortical brain structures in 38,851 individuals. Thalamus volume 34,464 European ancestry individuals 341 South East and East Asian ancestry individuals, 769 African American individuals Affymetrix, Illumina [NR] (imputed) 2 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST009669 Genome-wide genotyping array 2020-05-13 31816047 Boutin TS 2019-12-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31816047 Insights into the genetic basis of retinal detachment. Retinal detachment 2,893 British ancestry cases, 360,233 British ancestry controls NA Affymetrix, Illumina [7701827] (imputed) 3 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST009958 Genome-wide genotyping array 2020-05-13 31816047 Boutin TS 2019-12-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31816047 Insights into the genetic basis of retinal detachment. Retinal detachment or retinal break 3,977 British ancestry cases, 360,233 British ancestry controls NA Affymetrix, Illumina [7701827] (imputed) 27 retinal detachment, retinal break http://www.ebi.ac.uk/efo/EFO_0005773, http://www.ebi.ac.uk/efo/EFO_0010698 GCST009959 Genome-wide genotyping array 2020-05-13 31816047 Boutin TS 2019-12-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31816047 Insights into the genetic basis of retinal detachment. Retinal detachment with retinal break 1,380 British ancestry cases, 360,233 British ancestry controls NA Affymetrix, Illumina [7701827] (imputed) 1 rhegmatogenous retinal detachment http://www.ebi.ac.uk/efo/EFO_0005240 GCST009961 Genome-wide genotyping array 2020-05-13 31816047 Boutin TS 2019-12-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31816047 Insights into the genetic basis of retinal detachment. Retinal detachment or retinal break 6,141 European ancestry cases, 59,475 European ancestry controls 9,171 European ancestry cases, 406,168 European ancestry controls Affymetrix, Illumina [7581674] (imputed) 2 retinal detachment, retinal break http://www.ebi.ac.uk/efo/EFO_0005773, http://www.ebi.ac.uk/efo/EFO_0010698 GCST009960 Genome-wide genotyping array 2020-05-13 31816047 Boutin TS 2019-12-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31816047 Insights into the genetic basis of retinal detachment. High myopia 2,737 British ancestry cases, 47,635 British ancestry controls NA Affymetrix [NR] (imputed) 17 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST009962 Genome-wide genotyping array 2020-05-13 31816047 Boutin TS 2019-12-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31816047 Insights into the genetic basis of retinal detachment. Cataracts (operation) 21,679 British ancestry cases, 387,283 British ancestry controls NA Affymetrix [NR] (imputed) 20 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST009963 Genome-wide genotyping array 2020-07-31 32349335 Lundback V 2020-04-27 Cells www.ncbi.nlm.nih.gov/pubmed/32349335 Genome-Wide Association Study of Diabetogenic Adipose Morphology in the GENetics of Adipocyte Lipolysis (GENiAL) Cohort. Adipose morphology 894 individuals NA NR [9714326] (imputed) 30 adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004764 GCST010356 Genome-wide genotyping array 2020-03-03 28369058 Folkersen L 2017-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28369058 Mapping of 79 loci for 83 plasma protein biomarkers in cardiovascular disease. Blood protein levels in cardiovascular risk 3,394 European ancestry individuals 2,639 individuals Illumina [5270624] (imputed) 77 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST009731 Targeted genotyping array [Immunochip, Cardio-MetaboChip] 2020-01-07 31755958 Blauwendraat C 2019-11-22 Brain www.ncbi.nlm.nih.gov/pubmed/31755958 Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia. Parkinson's disease in GBA mutation carriers 1,588 European ancestry cases, 7,584 European ancestry controls up to 1,194 European ancestry cases, up to 13,901 European ancestry controls Illumina [NR] (imputed) 2 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST009373 Genome-wide genotyping array 2020-01-07 31755958 Blauwendraat C 2019-11-22 Brain www.ncbi.nlm.nih.gov/pubmed/31755958 Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia. Parkinson's disease in GBA mutation carriers (age at onset) 1,353 European ancestry cases NA Illumina [NR] (imputed) 0 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST009374 Genome-wide genotyping array 2019-12-05 30715261 Brouwer WP 2019-02-02 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/30715261 Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study. Response to (pegylated) interferon in HBeAg-negative hepatitis B 161 Asian, European, African and other ancestry cases, 253 Asian, European, African and other ancestry controls NA Illumina [8102086] (imputed) 4 response to interferon http://www.ebi.ac.uk/efo/EFO_0007859 GCST009172 Genome-wide genotyping array 2019-12-05 30715261 Brouwer WP 2019-02-02 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/30715261 Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study. Response to (pegylated) interferon in HBeAG-positive hepatitis B 121 Asian, European, African and other ancestry cases, 388 Asian, European, African and other ancestry controls NA Illumina [8102086] (imputed) 2 response to interferon http://www.ebi.ac.uk/efo/EFO_0007859 GCST009173 Genome-wide genotyping array 2019-12-05 30715261 Brouwer WP 2019-02-02 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/30715261 Genome Wide Association Study Identifies Genetic Variants Associated With Early And Sustained Response To (Peg)Interferon In Chronic Hepatitis B Patients: The GIANT-B Study. Response to (pegylated) interferon in chronic hepatitis B 282 Asian, European, African and other ancestry cases, 641 Asian, European, African and other ancestry controls NA Illumina [8102086] (imputed) 3 response to interferon http://www.ebi.ac.uk/efo/EFO_0007859 GCST009174 Genome-wide genotyping array 2020-08-17 31926635 Coleman JRI 2019-11-01 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31926635 The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls. Bipolar disorder or major depressive disorder 164,933 European ancestry major depressive disorder cases, 20,352 European ancestry bipolar disorder cases, 439,741 European ancestry controls NA NR [NR] (imputed) 92 unipolar depression, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985 GCST010416 Genome-wide genotyping array 2021-02-23 33407418 Jonsson A 2021-01-06 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33407418 Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test. Glucagon levels in response to oral glucose tolerance test (decremental area under the curve for 0-30 minutes) 553 European ancestry individuals, 1,346 individuals NA Illumina [NR] (imputed) 10 glucagon measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008463, http://www.ebi.ac.uk/efo/EFO_0004307 GCST011140 Genome-wide genotyping array 2021-02-23 33407418 Jonsson A 2021-01-06 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33407418 Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test. Glucagon levels in response to oral glucose tolerance test (decremental area under the curve for 0-120 minutes) 553 European ancestry individuals, 1,346 individuals NA Illumina [NR] (imputed) 11 glucagon measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008463, http://www.ebi.ac.uk/efo/EFO_0004307 GCST011139 Genome-wide genotyping array 2021-02-23 33407418 Jonsson A 2021-01-06 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33407418 Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test. Glucagon levels in response to oral glucose tolerance test (fasting) 553 European ancestry individuals, 1,346 individuals NA Illumina [NR] (imputed) 23 glucagon measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008463, http://www.ebi.ac.uk/efo/EFO_0004307 GCST011138 Genome-wide genotyping array 2021-02-23 33407418 Jonsson A 2021-01-06 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33407418 Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test. Glucagon levels in response to oral glucose tolerance test (30 minutes) 553 European ancestry individuals, 1,346 individuals NA Illumina [NR] (imputed) 11 glucagon measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008463, http://www.ebi.ac.uk/efo/EFO_0004307 GCST011137 Genome-wide genotyping array 2021-02-23 33407418 Jonsson A 2021-01-06 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33407418 Genome-wide association study of circulating levels of glucagon during an oral glucose tolerance test. Glucagon levels in response to oral glucose tolerance test (120 minutes) 553 European ancestry individuals, 1,346 individuals NA Illumina [NR] (imputed) 29 glucagon measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0008463, http://www.ebi.ac.uk/efo/EFO_0004307 GCST011136 Genome-wide genotyping array 2019-12-18 31748705 Ohta Y 2019-11-20 Hypertens Res www.ncbi.nlm.nih.gov/pubmed/31748705 Genetic factors associated with elevation of uric acid after treatment with thiazide-like diuretic in patients with essential hypertension. Uric acid elevation in response to thiazide-like diuretic in hypertension 73 Japanese ancestry responders, 53 Japanese ancestry non-responders NA Affymetrix [290698] 2 response to diuretic, uric acid measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0004761 GCST009319 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum total polyunsaturated fatty acid concentration in metabolic syndrome 426 Mediterranean individuals NA Illumina [621723] 3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST010319 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum omega-3 polyunsaturated fatty acid concentration in metabolic syndrome 426 Mediterranean individuals NA Illumina [621723] 10 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST010318 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum omega-6 polyunsaturated fatty acid concentration in metabolic syndrome 426 Mediterranean individuals NA Illumina [621723] 4 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST010317 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum docosahexaenoic fatty acid concentration in metabolic syndrome 426 Mediterranean individuals NA Illumina [621723] 11 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST010316 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum linoleic acid concentration in metabolic syndrome 426 Mediterranean individuals NA Illumina [621723] 6 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST010315 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum omega-6 to omega-3 polyunsaturated fatty acid ratio in metabolic syndrome 426 Mediterranean individuals NA Illumina [621723] 8 omega-6:omega-3 polyunsaturated fatty acid ratio http://www.ebi.ac.uk/efo/EFO_0010732 GCST010314 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum polyunsaturated fatty acid concentration x sex interaction in metabolic syndrome 239 Mediterranean women, 187 Mediterranean men NA Illumina [621723] 10 polyunsaturated fatty acid measurement, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0010733, http://www.ebi.ac.uk/efo/EFO_0008343 GCST010313 Genome-wide genotyping array 2020-07-24 31991592 Coltell O 2020-01-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/31991592 Genome-Wide Association Study for Serum Omega-3 and Omega-6 Polyunsaturated Fatty Acids: Exploratory Analysis of the Sex-Specific Effects and Dietary Modulation in Mediterranean Subjects with Metabolic Syndrome. Serum polyunsaturated fatty acid concentration x Mediterranean diet adherence interaction in metabolic syndrome 248 Mediterranean individuals with low adherence to Mediterranean diet, 178 Mediterranean individuals with high adherence to Mediterranean diet NA Illumina [621723] 19 polyunsaturated fatty acid measurement, diet measurement http://www.ebi.ac.uk/efo/EFO_0010733, http://www.ebi.ac.uk/efo/EFO_0008111 GCST010312 Genome-wide genotyping array 2020-02-21 31935283 Du Z 2020-01-01 Blood Adv www.ncbi.nlm.nih.gov/pubmed/31935283 A meta-analysis of genome-wide association studies of multiple myeloma among men and women of African ancestry. Multiple myeloma 1,813 African American and African ancestry cases, 8,871 African American and African ancestry controls NA Illumina [12683648] (imputed) 10 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST009680 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function in heavy smokers (low FEV1 vs high FEV1) 9,748 European ancestry individuals with low FEV1 measurements, 4,906 European ancestry individuals with high FEV1 measurements NA Affymetrix [28509962] (imputed) 5 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008659 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function in never smokers (high FEV1 vs average FEV1) 4,902 European ancestry individuals with high FEV1 measurements, 9,827 European ancestry individuals with average FEV1 measurements NA Affymetrix [28509962] (imputed) 8 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008660 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function in heavy smokers (high FEV1 vs average FEV1) 4,906 European ancestry individuals with high FEV1 measurements, 9,803 European ancestry individuals with average FEV1 measurements NA Affymetrix [28509962] (imputed) 3 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008661 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function in never smokers (low FEV1 vs average FEV1) 9,745 European ancestry individuals with low FEV1 measurements, 9,827 European ancestry individuals with average FEV1 measurements NA Affymetrix [28509962] (imputed) 4 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008663 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function in heavy smokers (low FEV1 vs average FEV1) 9,748 European ancestry individuals with low FEV1 measurements, 9,803 European ancestry individuals with average FEV1 measurements NA Affymetrix [28509962] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008665 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Smoking status (heavy vs never) 24,457 European ancestry heavy smokers, 24,474 European ancestry never smokers NA Affymetrix [28509962] (imputed) 13 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST008667 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function (low FEV1 vs high FEV1) x smoking interaction 9,745 European ancestry never smokers with low FEV1 measurements, 4,902 European ancestry never smokers with high FEV1 measurements, 9,748 European ancestry heavy smokers with low FEV1 measurements, 4,906 European ancestry heavy smokers with high FEV1 measurements NA Affymetrix [28509962] (imputed) 15 smoking status measurement, forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004314 GCST008666 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function (low FEV1 vs high FEV1) 19,493 European ancestry individuals with low FEV1 measurements, 9,808 European ancestry individuals with high FEV1 measurements NA Affymetrix [28509962] (imputed) 17 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008664 Genome-wide genotyping array 2019-09-13 26423011 Wain LV 2015-09-27 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/26423011 Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. Lung function in never smokers (low FEV1 vs high FEV1) 9,745 European ancestry individuals with low FEV1 measurements, 4,902 European ancestry individuals with high FEV1 measurements NA Affymetrix [28509962] (imputed) 18 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008662 Genome-wide genotyping array 2020-01-29 31694877 Nishida Y 2019-11-06 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/31694877 The interaction between ABCA1 polymorphism and physical activity on the HDL-cholesterol levels in a Japanese population. HDL cholesterol levels 2,231 Japanese ancestry men 2,599 Japanese ancestry men Illumina [7094228] (imputed) 5 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009528 Genome-wide genotyping array 2020-01-29 31694877 Nishida Y 2019-11-06 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/31694877 The interaction between ABCA1 polymorphism and physical activity on the HDL-cholesterol levels in a Japanese population. HDL cholesterol levels 2,431 Japanese ancestry women 3,109 Japanese ancestry women Illumina [7094228] (imputed) 5 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009527 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. HDL cholesterol levels x long total sleep time interaction (2df test) 2,933 African American long sleepers, 364 Chinese ancestry long sleepers, 112 Asian ancestry long sleepers, up to 7,870 European ancestry long sleepers, 1,038 Hispanic/Latino long sleepers, up to 11,975 African American controls, 1,449 Chinese ancestry controls, 454 Asian ancestry controls, at least 32,171 European ancestry controls, 4,091 Hispanic/Latino controls at least 217 African American long sleepers, 616 East Asian ancestry long sleepers, up to 9,486 European ancestry long sleepers, 2,515 Hispanic long sleepers, at least 929 African American controls, 2,517 East Asian ancestry controls, up to 38,126 European ancestry controls, 10,063 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 84 sleep duration, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004612 GCST009368 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Triglyceride levels x long total sleep time interaction (1df test) at least 2,926 African American long sleepers, 364 Chinese ancestry long sleepers, 112 Asian ancestry long sleepers, at least 7,664 European ancestry long sleepers, 1,038 Hispanic/Latino long sleepers, up to 11,906 African American controls, 1,449 Chinese ancestry controls, 454 Asian ancestry controls, at least 31,986 European ancestry controls, 4,091 Hispanic/Latino controls at least 217 African American long sleepers, 317 East Asian ancestry long sleepers, up to 5,171 European ancestry long sleepers, 2,515 Hispanic long sleepers, at least 928 African American controls, 1,301 East Asian ancestry controls, up to 20,961 European ancestry controls, 10,064 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 2 sleep duration, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004530 GCST009358 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. HDL cholesterol levels x short total sleep time interaction (2df test) 3,007 African American short sleepers, 369 Chinese ancestry short sleepers, 114 Asian ancestry short sleepers, at least 8,474 European ancestry short sleepers, 1,082 Hispanic/Latino short sleepers, up to 11,901 African American controls, 1,444 Chinese ancestry controls, 452 Asian ancestry controls, at least 31,567 European ancestry controls, 4,047 Hispanic/Latino controls up to 221 African American short sleepers, 629 East Asian ancestry short sleepers, up to 9,585 European ancestry short sleepers, 2,517 Hispanic short sleepers, at least 925 African American controls, 2,504 East Asian ancestry controls, up to 38,027 European ancestry controls, 10,061 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 91 sleep duration, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004612 GCST009367 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. LDL cholesterol levels x long total sleep time interaction (2df test) 2,913 African American long sleepers, 358 Chinese ancestry long sleepers, 110 Asian ancestry long sleepers, 7,583 European ancestry long sleepers, 1,036 Hispanic/Latino long sleepers, up to 11,862 African American controls, 1,432 Chinese ancestry controls, 444 Asian ancestry controls, at least 31,744 European ancestry controls, 4,066 Hispanic/Latino controls at least 214 African American long sleepers, 616 East Asian ancestry long sleepers, up to 6,657 European ancestry long sleepers, 2,457 Hispanic long sleepers, at least 913 African American controls, 2,517 East Asian ancestry controls, up to 26,868 European ancestry controls, 9,870 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 61 sleep duration, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004611 GCST009366 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. LDL cholesterol levels x short total sleep time interaction (2df test) 2,974 African American short sleepers, 365 Chinese ancestry short sleepers, 110 Asian ancestry short sleepers, at least 8,230 European ancestry short sleepers, 1,079 Hispanic/Latino short sleepers, 11,801 African American controls, 1,425 Chinese ancestry controls, 444 Asian ancestry controls, at least 31,097 European ancestry controls, 4,023 Hispanic/Latino controls at least 214 African American short sleepers, 629 East Asian ancestry short sleepers, up to 6,761 European ancestry short sleepers, 2,473 Hispanic short sleepers, at least 913 African American controls, 2,504 East Asian ancestry controls, up to 26,764 European ancestry controls, 9,854 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 71 sleep duration, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004611 GCST009365 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Triglyceride levels x long total sleep time interaction (2df test) at least 2,926 African American long sleepers, 364 Chinese ancestry long sleepers, 112 Asian ancestry long sleepers, at least 7,664 European ancestry long sleepers, 1,038 Hispanic/Latino long sleepers, up to 11,906 African American controls, 1,449 Chinese ancestry controls, 454 Asian ancestry controls, at least 31,986 European ancestry controls, 4,091 Hispanic/Latino controls at least 217 African American long sleepers, 317 East Asian ancestry long sleepers, up to 5,171 European ancestry long sleepers, 2,515 Hispanic long sleepers, at least 928 African American controls, 1,301 East Asian ancestry controls, up to 20,961 European ancestry controls, 10,064 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 58 sleep duration, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004530 GCST009364 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Triglyceride levels x short total sleep time interaction (2df test) 2,990 African American short sleepers, 369 Chinese ancestry short sleepers, 114 Asian ancestry short sleepers, at least 8,300 European ancestry short sleepers, 1,082 Hispanic/Latino short sleepers, at least 11,842 African American controls, 1,444 Chinese ancestry controls, 452 Asian ancestry controls, at least 31,350 European ancestry controls, 4,047 Hispanic/Latino controls at least 220 African American short sleepers, 326 East Asian ancestry short sleepers, up to 5,288 European ancestry short sleepers, 2,517 Hispanic short sleepers, at least 925 African American controls, 1,292 East Asian ancestry controls, up to 20,844 European ancestry controls, 10,062 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 63 sleep duration, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004530 GCST009363 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. HDL cholesterol levels x long total sleep time interaction (1df test) 2,933 African American long sleepers, 364 Chinese ancestry long sleepers, 112 Asian ancestry long sleepers, up to 7,870 European ancestry long sleepers, 1,038 Hispanic/Latino long sleepers, up to 11,975 African American controls, 1,449 Chinese ancestry controls, 454 Asian ancestry controls, at least 32,171 European ancestry controls, 4,091 Hispanic/Latino controls at least 217 African American long sleepers, 616 East Asian ancestry long sleepers, up to 9,486 European ancestry long sleepers, 2,515 Hispanic long sleepers, at least 929 African American controls, 2,517 East Asian ancestry controls, up to 38,126 European ancestry controls, 10,063 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 3 sleep duration, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004612 GCST009362 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Triglyceride levels 14,832 African American individuals, 1,813 Chinese ancestry individuals, 566 Asian ancestry individuals, 39,650 European ancestry individuals, 5,129 Hispanic/Latino individuals NA Affymetrix, Illumina [up to 2533153] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST009370 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. Triglyceride levels x short total sleep time interaction (1df test) 2,990 African American short sleepers, 369 Chinese ancestry short sleepers, 114 Asian ancestry short sleepers, at least 8,300 European ancestry short sleepers, 1,082 Hispanic/Latino short sleepers, at least 11,842 African American controls, 1,444 Chinese ancestry controls, 452 Asian ancestry controls, at least 31,350 European ancestry controls, 4,047 Hispanic/Latino controls at least 220 African American short sleepers, 326 East Asian ancestry short sleepers, up to 5,288 European ancestry short sleepers, 2,517 Hispanic short sleepers, at least 925 African American controls, 1,292 East Asian ancestry controls, up to 20,844 European ancestry controls, 10,062 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 2 sleep duration, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004530 GCST009369 Genome-wide genotyping array 2019-12-17 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. HDL cholesterol levels 14,908 African American individuals, 1,813 Chinese ancestry individuals, 566 Asian ancestry individuals, 40,041 European ancestry individuals, 5,129 Hispanic/Latino individuals NA Affymetrix, Illumina [up to 2533153] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009316 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. HDL cholesterol levels x short total sleep time interaction (1df test) 3,007 African American short sleepers, 369 Chinese ancestry short sleepers, 114 Asian ancestry short sleepers, at least 8,474 European ancestry short sleepers, 1,082 Hispanic/Latino short sleepers, up to 11,901 African American controls, 1,444 Chinese ancestry controls, 452 Asian ancestry controls, at least 31,567 European ancestry controls, 4,047 Hispanic/Latino controls up to 221 African American short sleepers, 629 East Asian ancestry short sleepers, up to 9,585 European ancestry short sleepers, 2,517 Hispanic short sleepers, at least 925 African American controls, 2,504 East Asian ancestry controls, up to 38,027 European ancestry controls, 10,061 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 1 sleep duration, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004612 GCST009361 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. LDL cholesterol levels x long total sleep time interaction (1df test) 2,913 African American long sleepers, 358 Chinese ancestry long sleepers, 110 Asian ancestry long sleepers, 7,583 European ancestry long sleepers, 1,036 Hispanic/Latino long sleepers, up to 11,862 African American controls, 1,432 Chinese ancestry controls, 444 Asian ancestry controls, at least 31,744 European ancestry controls, 4,066 Hispanic/Latino controls at least 214 African American long sleepers, 616 East Asian ancestry long sleepers, up to 6,657 European ancestry long sleepers, 2,457 Hispanic long sleepers, at least 913 African American controls, 2,517 East Asian ancestry controls, up to 26,868 European ancestry controls, 9,870 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 3 sleep duration, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004611 GCST009360 Genome-wide genotyping array 2019-12-17 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. LDL cholesterol levels 14,775 African American individuals, 1,790 Chinese ancestry individuals, 554 Asian ancestry individuals, 39,327 European ancestry individuals, 5,102 Hispanic/Latino individuals NA Affymetrix, Illumina [up to 2533153] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST009317 Genome-wide genotyping array 2020-01-07 31719535 Noordam R 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719535 Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration. LDL cholesterol levels x short total sleep time interaction (1df test) 2,974 African American short sleepers, 365 Chinese ancestry short sleepers, 110 Asian ancestry short sleepers, at least 8,230 European ancestry short sleepers, 1,079 Hispanic/Latino short sleepers, 11,801 African American controls, 1,425 Chinese ancestry controls, 444 Asian ancestry controls, at least 31,097 European ancestry controls, 4,023 Hispanic/Latino controls at least 214 African American short sleepers, 629 East Asian ancestry short sleepers, up to 6,761 European ancestry short sleepers, 2,473 Hispanic short sleepers, at least 913 African American controls, 2,504 East Asian ancestry controls, up to 26,764 European ancestry controls, 9,854 Hispanic controls Affymetrix, Illumina [up to 2533153] (imputed) 2 sleep duration, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004611 GCST009359 Genome-wide genotyping array 2020-07-14 32154731 Ripatti P 2020-03-10 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32154731 Polygenic Hyperlipidemias and Coronary Artery Disease Risk. Low density lipoprotein cholesterol levels 324,708 British ancestry individuals NA Affymetrix [5701386] (imputed) 217 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST010204 Genome-wide genotyping array 2020-07-09 32154731 Ripatti P 2020-03-10 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32154731 Polygenic Hyperlipidemias and Coronary Artery Disease Risk. Triglyceride levels 324,694 British ancestry individuals NA Affymetrix [5701386] (imputed) 183 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST010173 Genome-wide genotyping array 2020-01-27 31660654 Bandres-Ciga S 2019-10-29 Mov Disord www.ncbi.nlm.nih.gov/pubmed/31660654 The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight. Parkinson's disease (age of onset) 3,997 Spanish ancestry individuals NA Illumina [9911207] (imputed) 2 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST009513 Genome-wide genotyping array 2020-01-27 31660654 Bandres-Ciga S 2019-10-29 Mov Disord www.ncbi.nlm.nih.gov/pubmed/31660654 The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight. Parkinson's disease 4,639 Spanish ancestry cases, 2,949 Spanish ancestry controls NA Illumina [9911207] (imputed) 7 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST009512 Genome-wide genotyping array 2020-03-09 31710517 Allen RJ 2019-11-11 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/31710517 Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis. Idiopathic pulmonary fibrosis 2,668 European ancestry cases, 8,591 European ancestry controls 1,456 European ancestry cases, 11,874 European ancestry controls Affymetrix, Illumina [10790934] (imputed) 17 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST009758 Genome-wide genotyping array 2020-01-22 31763980 Xiong Z 2019-11-25 Elife www.ncbi.nlm.nih.gov/pubmed/31763980 Novel genetic loci affecting facial shape variation in humans. Facial morphology 10,115 European ancestry individuals NA Illumina [7029494] (imputed) 41 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST009464 Genome-wide genotyping array 2020-03-03 29926116 Grarup N 2018-06-20 Diabetologia www.ncbi.nlm.nih.gov/pubmed/29926116 Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population. Type 2 diabetes 317 Greenlandic ancestry cases, 2,631 Greenlandic ancestry controls NA Illumina [115182] 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST009732 Targeted genotyping array [Metabochip] 2020-06-05 32310270 Foo JN 2020-04-20 JAMA Neurol www.ncbi.nlm.nih.gov/pubmed/32310270 Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study. Parkinson's disease 6,724 East Asian ancestry cases, 24,851 East Asian ancestry controls 57,545 European ancestry cases, 1,868,816 European ancestry controls, 988 Japanese ancestry cases, 2,521 Japanese ancestry controls Illumina [5843213] (imputed) 10 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST010049 Genome-wide genotyping array 2021-04-27 32929176 Feng GJ 2020-09-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32929176 Identification of pleiotropic loci underlying hip bone mineral density and trunk lean mass. Bone mineral density or trunk lean mass (pleiotropy) 8,508 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals 215,234 European ancestry individuals Affymetrix [12061510] (imputed) 1 bone density, lean body mass http://www.ebi.ac.uk/efo/EFO_0003923, http://www.ebi.ac.uk/efo/EFO_0004995 GCST011561 Genome-wide genotyping array 2021-04-27 32929176 Feng GJ 2020-09-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32929176 Identification of pleiotropic loci underlying hip bone mineral density and trunk lean mass. Trunk lean mass 8,508 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals 215,234 European ancestry individuals Affymetrix [12061510] (imputed) 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST011560 Genome-wide genotyping array 2021-04-27 32929176 Feng GJ 2020-09-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32929176 Identification of pleiotropic loci underlying hip bone mineral density and trunk lean mass. Bone mineral density 8,508 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals 215,234 European ancestry individuals Affymetrix [12061510] (imputed) 3 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST011559 Genome-wide genotyping array 2020-06-17 32327693 Oskarsson GR 2020-04-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32327693 Predicted loss and gain of function mutations in ACO1 are associated with erythropoiesis. Hemoglobin levels 684,122 European ancestry individuals NA Affymetrix, Illumina [43000000] (imputed) 362 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST010083 Genome-wide genotyping array, Genome-wide sequencing 2019-12-10 31636271 Gallois A 2019-10-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31636271 A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context. Serum metabolite levels (CMS) 6,263 Finnish ancestry men NA Illumina [609262] 588 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST009240 Genome-wide genotyping array 2019-12-10 31636271 Gallois A 2019-10-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31636271 A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context. Change in serum metabolite levels 3,351 Finnish ancestry men NA Illumina [609262] 7 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST009241 Genome-wide genotyping array 2019-12-10 31636271 Gallois A 2019-10-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31636271 A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context. Change in serum metabolite levels (CMS) 3,351 Finnish ancestry men NA Illumina [609262] 8 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST009239 Genome-wide genotyping array 2019-12-10 31636271 Gallois A 2019-10-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31636271 A comprehensive study of metabolite genetics reveals strong pleiotropy and heterogeneity across time and context. Serum metabolite levels 6,263 Finnish ancestry men NA Illumina [609262] 474 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST009242 Genome-wide genotyping array 2020-07-24 32355309 Cha PC 2020-05-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32355309 Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients. Levodopa wearing off effect (time symptoms uncontrolled) in Parkinson's disease (response to zonisamide) 67 Japanese ancestry responders, 133 Japanese ancestry poor responders NA Illumina [611492] 4 motor function measurement, response to zonisamide, response to levodopa http://www.ebi.ac.uk/efo/EFO_0010749, http://www.ebi.ac.uk/efo/EFO_0010748, http://www.ebi.ac.uk/efo/EFO_0010747 GCST010322 Genome-wide genotyping array 2020-07-24 32355309 Cha PC 2020-05-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32355309 Genome-wide association study identifies zonisamide responsive gene in Parkinson's disease patients. Levodopa wearing off effect (motor symptom score change) in Parkinson's disease (response to zonisamide) 67 Japanese ancestry responders, 133 Japanese ancestry poor responders NA Illumina [611492] 1 motor function measurement, response to zonisamide, response to levodopa http://www.ebi.ac.uk/efo/EFO_0010749, http://www.ebi.ac.uk/efo/EFO_0010748, http://www.ebi.ac.uk/efo/EFO_0010747 GCST010323 Genome-wide genotyping array 2020-06-03 32310165 Kim BH 2020-04-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/32310165 Identification of Novel Genes Associated with Cortical Thickness in Alzheimer's Disease: Systems Biology Approach to Neuroimaging Endophenotype. Cortical thickness 919 European ancestry individuals NA Illumina [3041429] (imputed) 2 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST010041 Genome-wide genotyping array 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Leucine-rich repeats and immunoglobulin-like domains protein 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010323 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Low-density lipoprotein receptor-related protein 11 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010324 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Multiple coagulation factor deficiency protein 2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010325 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Meprin A subunit beta levels 1,200 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010326 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Meteorin-like protein levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010327 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. NAD kinase levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010328 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Nectin-2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010329 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Nodal modulator 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010330 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Neural proliferation differentiation and control protein 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010331 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Neuronal pentraxin receptor levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010332 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Phosphoprotein associated with glycosphingolipid-enriched microdomains 1 levels 1,308 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010333 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Paired immunoglobulin-like type 2 receptor beta levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010334 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Protein phosphatase inhibitor 2 levels 1,300 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010335 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Dihydropteridine reductase levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010336 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Regenerating islet-derived protein 4 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010337 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Eosinophil cationic protein levels 1,309 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010338 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Inactive tyrosine-protein kinase transmembrane receptor ROR1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010339 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Reticulon-4 receptor levels 1,312 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010340 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Protein S100-A12 levels 1,100 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010341 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Syndecan-4 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010342 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Semaphorin-3F levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010343 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Serpin B6 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010344 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Serpin B8 levels 1,254 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010345 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Sialic acid-binding Ig-like lectin 7 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010346 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Synaptosomal-associated protein 23 levels 909 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010347 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Ectonucleoside triphosphate diphosphohydrolase 5 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010310 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Protein FAM3C levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010311 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Fructose-1,6-bisphosphatase 1 levels 1,174 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010312 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Fc receptor-like protein 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010313 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Peptidyl-prolyl cis-trans isomerase FKBP4 levels 1,120 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010314 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Galanin peptide levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010315 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Glutaredoxin-1 levels 1,227 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010316 Genome-wide sequencing [22x] 2019-03-28 30664655 Adhikari K 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664655 A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Eye color (hue) 6,236 Latin American individuals NA Illumina [8896142] (imputed) 3 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007456 Genome-wide genotyping array 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Scavenger receptor cysteine-rich type 1 protein M130 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010198 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Complement component C1q receptor levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010199 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cadherin-5 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010200 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Chitinase-3-like protein 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010201 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Chitotriosidase-1 levels 1,184 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010202 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Contactin-1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010203 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Collagen alpha-1 (I) chain levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010204 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Carboxypeptidase A1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010205 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Carboxypeptidase B levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010206 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cystatin-B levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010207 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cathepsin D levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010208 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cathepsin Z levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010209 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-X-C motif chemokine 16 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010210 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Protein delta homolog 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010211 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Epidermal growth factor levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010212 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. epithelial cell adhesion molecule levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010213 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Ephrin type-B receptor 4 levels 1,322 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010214 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Fatty acid-binding protein, adipocyte levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010215 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor superfamily member 6 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010216 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Galectin-3 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010217 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Galectin-4 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010218 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Granulins levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010219 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Intercellular adhesion molecule 2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010220 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Insulin-like growth factor-binding protein 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010221 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Insulin-like growth factor-binding protein 2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010222 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-type lectin domain family 5 member A levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010298 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. CXADR-like membrane protein levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010299 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Calsyntenin-2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010300 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Clusterin-like protein 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010301 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Catechol O-methyltransferase levels 1,239 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010302 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Crk-like protein levels 1,105 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010303 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Pro-cathepsin H levels 1,278 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010304 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cathepsin O levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010305 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Aromatic-L-amino-acid decarboxylase levels 180 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010306 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Dipeptidyl peptidase 2 levels 1,290 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010307 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Gamma-enolase levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010308 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010309 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. GRB2-related adapter protein 2 levels 923 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010317 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Insulin-like growth factor-binding protein-like 1 levels 1,312 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010318 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Integrin beta-7 levels 1,211 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010319 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Kallikrein-10 levels 1,312 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010320 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Kynurenine-oxoglutarate transaminase 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010321 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Leukocyte immunoglobulin-like receptor subfamily A member 5 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010322 Genome-wide sequencing [22x] 2019-03-28 30664655 Adhikari K 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664655 A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Skin pigmentation 6,236 Latin American individuals NA Illumina [8896142] (imputed) 14 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST007452 Genome-wide genotyping array 2019-03-28 30664655 Adhikari K 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664655 A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Eye color (saturation) 6,236 Latin American individuals NA Illumina [8896142] (imputed) 10 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007457 Genome-wide genotyping array 2019-03-28 30664655 Adhikari K 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664655 A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Eye color 6,236 Latin American individuals NA Illumina [8896142] (imputed) 9 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007453 Genome-wide genotyping array 2019-03-28 30664655 Adhikari K 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664655 A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Hair color 6,236 Latin American individuals NA Illumina [8896142] (imputed) 7 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST007454 Genome-wide genotyping array 2019-03-28 30664655 Adhikari K 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664655 A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Eye color (brightness) 6,236 Latin American individuals NA Illumina [8896142] (imputed) 11 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007455 Genome-wide genotyping array 2019-03-28 30664655 Adhikari K 2019-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30664655 A GWAS in Latin Americans highlights the convergent evolution of lighter skin pigmentation in Eurasia. Skin, hair and eye pigmentation (multivariate analysis) 6,236 Latin American individuals NA Illumina [181139] (imputed) 11 hair colour measurement, eye colour measurement, skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007822, http://www.ebi.ac.uk/efo/EFO_0009764, http://www.ebi.ac.uk/efo/EFO_0007009 GCST007451 Genome-wide genotyping array 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tartrate-resistant acid phosphatase type 5 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010273 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Urokinase-type plasminogen activator levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010274 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Urokinase plasminogen activator surface receptor levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010275 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. vWF levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010276 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Lysophosphatidic acid phosphatase type 6 levels 1,311 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010277 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Adhesion G protein-coupled receptor E2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010278 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Adhesion G-protein coupled receptor G2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010279 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Retinal dehydrogenase 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010280 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Angiopoietin-2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010281 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Angiopoietin-related protein 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010282 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Angiopoietin-related protein 7 levels 1,306 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010283 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. DNA-(apurinic or apyrimidinic site) lyase levels 1,187 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010284 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Amyloid-like protein 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010285 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Arginase-1 levels 1,072 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010286 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Large proline-rich protein BAG6 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010287 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Carbonic anhydrase 13 levels 1,248 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010288 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Soluble calcium-activated nucleotidase 1 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010289 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Coiled-coil domain-containing protein 80 levels 1,309 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010290 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Sialomucin core protein 24 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010291 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. T-cell surface glycoprotein CD1c levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010292 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. CD2-associated protein levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010293 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. B-cell antigen receptor complex-associated protein beta chain levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010294 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cadherin-2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010295 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cadherin-related family member 5 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010296 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Chordin-like protein 2 levels 1,279 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010297 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Platelet endothelial cell adhesion molecule levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010248 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Peptidoglycan recognition protein 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010249 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Elafin levels 1,322 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010250 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Perlecan levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010251 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Paraoxonase activity 1,322 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010252 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Myeloblastin levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010253 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Pulmonary surfactant-associated protein D levels 1,316 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010254 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Retinoic acid receptor responder protein 2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010255 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Resistin levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010256 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Secretoglobin family 3A member 2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010257 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. E-selectin levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010258 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. P-selectin levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010259 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tyrosine-protein phosphatase non-receptor type substrate 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010260 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Spondin-1 levels 1,314 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010261 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. ST2 protein levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010262 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tissue factor pathway inhibitor levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010263 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Metalloproteinase inhibitor 4 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010264 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Trem-like transcript 2 protein levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010265 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010266 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor 2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010267 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor superfamily member 10C levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010268 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor receptor superfamily member 14 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010269 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tumor necrosis factor ligand superfamily member 13B levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010270 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tissue-type plasminogen activator levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010271 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Transferrin receptor protein 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010272 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Insulin-like growth factor-binding protein 7 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010223 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-17 receptor A levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010224 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-18-binding protein levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010225 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-1 receptor type 1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010226 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-1 receptor type 2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010227 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-2 receptor subunit alpha levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010228 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-6 receptor subunit alpha levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010229 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Integrin beta-2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010230 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Junctional adhesion molecule A levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010231 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Kallikrein-6 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010232 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Low-density lipoprotein receptor levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010233 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Lymphotoxin-beta receptor levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010234 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Myoglobin levels 1,322 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010235 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Monocyte chemoattractant protein-1 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010236 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Matrix extracellular phosphoglycoprotein levels 974 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010237 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Matrix metalloproteinase-2 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010238 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Matrix metalloproteinase-3 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010239 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Matrix metalloproteinase-9 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010240 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Myeloperoxidase levels 1,322 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010241 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Neurogenic locus notch homolog protein 3 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010242 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Osteoprotegerin levels 1,243 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010243 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Osteopontin levels 1,322 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010244 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Plasminogen activator inhibitor-1 (PAI-1) levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010245 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Proprotein convertase subtilisin/kexin type 9 levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010246 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Platelet-derived growth factor subunit A levels 1,323 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010247 Genome-wide sequencing [22x] 2020-01-28 31738830 McGraw KL 2019-11-01 Blood Adv www.ncbi.nlm.nih.gov/pubmed/31738830 Non-del(5q) myelodysplastic syndromes-associated loci detected by SNP-array genome-wide association meta-analysis. Non-del(5q) myelodysplastic syndromes 907 European ancestry cases, 5,605 European ancestry controls NA Affymetrix [7515136] (imputed) 8 myelodysplastic syndrome http://www.ebi.ac.uk/efo/EFO_0000198 GCST009516 Genome-wide genotyping array 2021-07-08 33393196 Soliai M 2021-01-03 Int Forum Allergy Rhinol www.ncbi.nlm.nih.gov/pubmed/33393196 Two-stage genome-wide association study of chronic rhinosinusitis and disease subphenotypes highlights mucosal immunity contributing to risk. Chronic rhinosinusitis 483 European ancestry cases, 2,057 European ancestry controls NA Illumina [4528849] (imputed) 6 chronic rhinosinusitis http://www.ebi.ac.uk/efo/EFO_1000024 GCST012015 Genome-wide genotyping array 2021-01-21 30909962 Zuo XY 2019-03-25 Biol Sex Differ www.ncbi.nlm.nih.gov/pubmed/30909962 X-chromosome association study reveals genetic susceptibility loci of nasopharyngeal carcinoma. Nasopharyngeal carcinoma 1,615 East Asian ancestry cases and 1,025 East Asian ancestry controls 543 East Asian ancestry cases, 735 East Asian ancestry controls Illumina [111307] (imputed) 0 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST010978 Targeted genotyping array 2021-02-18 33410475 Mangantig E 2021-01-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33410475 Germline variants are associated with increased primary melanoma tumor thickness at diagnosis. Breslow thickness in cutaneous melanoma 8,505 European ancestry individuals NA Illumina [13517544] (imputed) 1 Breslow thickness http://www.ebi.ac.uk/efo/EFO_0004955 GCST011123 Genome-wide genotyping array 2018-09-18 30031151 Virtanen VB 2018-07-18 Eur J Med Genet www.ncbi.nlm.nih.gov/pubmed/30031151 Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant. Hirschsprung disease 105 European ancestry cases, 386 European ancestry controls 154 Swedish ancestry cases, 177 European ancestry controls Illumina [8432870] (imputed) 0 Hirschsprung disease http://purl.obolibrary.org/obo/MONDO_0018309 GCST006272 Genome-wide genotyping array 2018-09-18 30031151 Virtanen VB 2018-07-18 Eur J Med Genet www.ncbi.nlm.nih.gov/pubmed/30031151 Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant. Hirschsprung disease 68 European ancestry cases, 386 European ancestry controls NA Illumina [8432870] (imputed) 1 Hirschsprung disease http://purl.obolibrary.org/obo/MONDO_0018309 GCST006271 Genome-wide genotyping array 2019-03-02 30680360 McCoy TH Jr 2018-05-29 JBMR Plus www.ncbi.nlm.nih.gov/pubmed/30680360 Genomewide Association Study of Fracture Nonunion Using Electronic Health Records. Nonunion in individuals with fractures 131 Northern European ancestry cases, 1,629 Northern European ancestry controls NA Illumina [893900] (imputed) 44 fractures, ununited http://www.ebi.ac.uk/efo/EFO_0009707 GCST007250 Genome-wide genotyping array 2020-01-08 31790847 Hou R 2019-11-29 Bone www.ncbi.nlm.nih.gov/pubmed/31790847 Genetic variants affecting bone mineral density and bone mineral content at multiple skeletal sites in Hispanic children. Bone mineral content 1,030 Hispanic or Latin American children NA Illumina [> 1100000] 29 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST009378 Genome-wide genotyping array, Exome-wide sequencing 2020-01-08 31790847 Hou R 2019-11-29 Bone www.ncbi.nlm.nih.gov/pubmed/31790847 Genetic variants affecting bone mineral density and bone mineral content at multiple skeletal sites in Hispanic children. Bone mineral density 1,030 Hispanic or Latin American children NA Illumina [> 1100000] 10 volumetric bone mineral density http://www.ebi.ac.uk/efo/EFO_0007620 GCST009377 Genome-wide genotyping array, Exome-wide sequencing 2020-02-06 31832568 Gawrieh S 2019-11-03 Hepatol Commun www.ncbi.nlm.nih.gov/pubmed/31832568 A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH. NASH resolution in nonalcoholic steatohepatitis 25 European ancestry cases, 116 European ancestry controls NA Illumina [5417859] (imputed) 4 remission http://www.ebi.ac.uk/efo/EFO_0009785 GCST009548 Genome-wide genotyping array 2020-02-06 31832568 Gawrieh S 2019-11-03 Hepatol Commun www.ncbi.nlm.nih.gov/pubmed/31832568 A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH. Pruritus in nonalcoholic steatohepatitis approximately 31 European ancestry cases, approximately 166 European ancestry controls NA Illumina [5417859] (imputed) 1 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST009549 Genome-wide genotyping array 2020-02-06 31832568 Gawrieh S 2019-11-03 Hepatol Commun www.ncbi.nlm.nih.gov/pubmed/31832568 A Pilot Genome-Wide Analysis Study Identifies Loci Associated With Response to Obeticholic Acid in Patients With NASH. Fibrosis improvement in nonalcoholic steatohepatitis 38 European ancestry cases, 103 European ancestry controls NA Illumina [5417859] (imputed) 2 liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0010576 GCST009547 Genome-wide genotyping array 2020-04-17 32019797 Wojcik GL 2020-02-04 mBio www.ncbi.nlm.nih.gov/pubmed/32019797 Genome-Wide Association Study of Cryptosporidiosis in Infants Implicates PRKCA. Cryptosporidiosis 183 Bangladeshi ancestry cases, 873 Bangladeshi ancestry controls NA Illumina [6504706] (imputed) 3 cryptosporidiosis http://purl.obolibrary.org/obo/MONDO_0015474 GCST009861 Genome-wide genotyping array 2020-03-30 31936517 Cox JW 2020-01-09 J Clin Med www.ncbi.nlm.nih.gov/pubmed/31936517 Genome-Wide Association Study of Opioid Cessation. Opioid use cessation 1,130 African American individuals, 2,919 European ancestry individuals NA Illumina [NR] (imputed) 7 Opioid use measurement http://www.ebi.ac.uk/efo/EFO_0009937 GCST009796 Genome-wide genotyping array 2018-10-17 30013184 Waage J 2018-07-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30013184 Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Allergic rhinitis 59,762 European and unknown ancestry cases, 152,358 European and unknown ancestry controls 60,720 European ancestry cases, 618,527 European ancestry controls Affymetrix, Illumina, Perlegen [16531985] (imputed) 44 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST006409 Genome-wide genotyping array 2018-10-17 30013184 Waage J 2018-07-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30013184 Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Allergic sensitization 8,040 European ancestry cases, 16,441 European ancestry controls NA Affymetrix, Illumina [16531985] (imputed) 19 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST006408 Genome-wide genotyping array 2018-10-25 30013184 Waage J 2018-07-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30013184 Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis. Non-allergic rhinitis 2,028 European and unknown ancestry cases, 9,606 European and unknown ancestry controls NA Affymetrix, Illumina [12291687] (imputed) 0 non-allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0009364 GCST006474 Genome-wide genotyping array 2019-12-11 31708768 Liu C 2019-10-25 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/31708768 Genome-Wide Association Studies for Cerebrospinal Fluid Soluble TREM2 in Alzheimer's Disease. Cerebrospinal fluid sTREM-2 levels 224 healthy normal individuals, 72 significant memory concern individuals, 234 early mild cognitive impairment individuals, 277 late mild cognitive impairment individuals, 194 Alzheimer's disease cases NA Illumina [2379855] 203 soluble triggering receptor expressed on myeloid cells 2 measurement http://www.ebi.ac.uk/efo/EFO_0010151 GCST009246 Genome-wide genotyping array 2020-07-14 31729902 Penney KL 2019-11-15 J Urol www.ncbi.nlm.nih.gov/pubmed/31729902 Genome-wide Association Study for Urinary and Fecal Incontinence in Women. Urinary incontinence 6,120 European ancestry female cases, 4,811 European ancestry female controls NA Affymetrix, Illumina [1410640] (imputed) 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST010205 Genome-wide genotyping array 2020-05-01 31729902 Penney KL 2019-11-15 J Urol www.ncbi.nlm.nih.gov/pubmed/31729902 Genome-wide Association Study for Urinary and Fecal Incontinence in Women. Stress urinary incontinence 1,809 European ancestry female cases, 4,811 European ancestry female controls NA Affymetrix, Illumina [1410640] (imputed) 1 Stress urinary incontinence http://purl.obolibrary.org/obo/HP_0010992 GCST009927 Genome-wide genotyping array 2020-07-14 31729902 Penney KL 2019-11-15 J Urol www.ncbi.nlm.nih.gov/pubmed/31729902 Genome-wide Association Study for Urinary and Fecal Incontinence in Women. Urgency urinary incontinence 1,942 European ancestry female cases, 4,811 European ancestry female controls NA Affymetrix, Illumina [1410640] (imputed) 0 urgency urinary incontinence http://www.ebi.ac.uk/efo/EFO_0006865 GCST009926 Genome-wide genotyping array 2020-05-01 31729902 Penney KL 2019-11-15 J Urol www.ncbi.nlm.nih.gov/pubmed/31729902 Genome-wide Association Study for Urinary and Fecal Incontinence in Women. Stress urinary incontinence and urgency urinary incontinence 2,036 European ancestry female cases, 4,811 European ancestry female controls NA Affymetrix, Illumina [1410640] (imputed) 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST009928 Genome-wide genotyping array 2020-05-01 31729902 Penney KL 2019-11-15 J Urol www.ncbi.nlm.nih.gov/pubmed/31729902 Genome-wide Association Study for Urinary and Fecal Incontinence in Women. Fecal incontinence 4,247 European ancestry female cases, 11,634 European ancestry female controls NA Affymetrix, Illumina [1410640] (imputed) 2 fecal incontinence http://www.ebi.ac.uk/efo/EFO_0009523 GCST009925 Genome-wide genotyping array 2021-01-11 33307546 Pairo-Castineira E 2020-12-11 Nature www.ncbi.nlm.nih.gov/pubmed/33307546 Genetic mechanisms of critical illness in Covid-19. COVID-19 (critical illness vs population) 2,804 European ancestry cases, 2,415 European, South Asian and Hispanic or Latin American ancestry cases, 687,911 European ancestry controls, 477,741 European, South Asian and Hispanic or Latin American ancestry controls NA Illumina [NR] (imputed) 6 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010936 Genome-wide genotyping array 2021-01-11 33307546 Pairo-Castineira E 2020-12-11 Nature www.ncbi.nlm.nih.gov/pubmed/33307546 Genetic mechanisms of critical illness in Covid-19. COVID-19 (critical illness vs population) 182 African ancestry cases, 910 African ancestry controls NA Illumina [4700000] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90013412 Genome-wide genotyping array 2021-01-11 33307546 Pairo-Castineira E 2020-12-11 Nature www.ncbi.nlm.nih.gov/pubmed/33307546 Genetic mechanisms of critical illness in Covid-19. COVID-19 (critical illness vs population) 149 East Asian ancestry cases, 745 East Asian ancestry controls NA Illumina [4700000] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90013413 Genome-wide genotyping array 2021-01-11 33307546 Pairo-Castineira E 2020-12-11 Nature www.ncbi.nlm.nih.gov/pubmed/33307546 Genetic mechanisms of critical illness in Covid-19. COVID-19 (critical illness vs population) 1,676 European ancestry cases, 8,380 European ancestry controls 2,415 European, South Asian and Hispanic or Latin American ancestry cases, 477,741 European, South Asian and Hispanic or Latin American ancestry controls, 1,128 European ancestry cases, 679,531 European ancestry controls Illumina [4700000] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90013414 Genome-wide genotyping array 2021-01-11 33307546 Pairo-Castineira E 2020-12-11 Nature www.ncbi.nlm.nih.gov/pubmed/33307546 Genetic mechanisms of critical illness in Covid-19. COVID-19 (critical illness vs population) 237 South Asian ancestry cases, 1,185 South Asian ancestry controls NA Illumina [4700000] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90013415 Genome-wide genotyping array 2020-07-23 32314116 Zhang H 2020-04-20 Osteoporos Int www.ncbi.nlm.nih.gov/pubmed/32314116 Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis. Bone mineral density (hip) 3,267 European ancestry individuals, 1,619 Chinese ancestry individuals, 843 African American individuals, 446 Hispanic individuals NA Affymetrix, Illumina [NR] (imputed) 4 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST010301 Genome-wide genotyping array 2020-07-23 32314116 Zhang H 2020-04-20 Osteoporos Int www.ncbi.nlm.nih.gov/pubmed/32314116 Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis. Hip bone size 3,267 European ancestry individuals, 1,619 Chinese ancestry individuals, 843 African American individuals, 446 Hispanic individuals NA Affymetrix, Illumina [NR] (imputed) 33 hip bone size http://www.ebi.ac.uk/efo/EFO_0004844 GCST010300 Genome-wide genotyping array 2020-07-23 32314116 Zhang H 2020-04-20 Osteoporos Int www.ncbi.nlm.nih.gov/pubmed/32314116 Pleiotropic loci underlying bone mineral density and bone size identified by a bivariate genome-wide association analysis. Bone mineral density (hip) and hip bone size 3,267 European ancestry individuals, 1,619 Chinese ancestry individuals, 843 African American individuals, 446 Hispanic individuals NA Affymetrix, Illumina [NR] (imputed) 34 hip bone mineral density, hip bone size http://www.ebi.ac.uk/efo/EFO_0007702, http://www.ebi.ac.uk/efo/EFO_0004844 GCST010299 Genome-wide genotyping array 2021-07-13 33048379 Richard MA 2020-10-13 Cancer www.ncbi.nlm.nih.gov/pubmed/33048379 Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort. BMI in adult survivors of childhood acute lymphoblastic leukemia treated with cranial radiation 962 European ancestry individuals 260 individuals Illumina [> 9000000] (imputed) 2 body mass index, response to cranial radiation therapy http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0010950 GCST012027 Genome-wide genotyping array 2021-07-13 33048379 Richard MA 2020-10-13 Cancer www.ncbi.nlm.nih.gov/pubmed/33048379 Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort. BMI in adult survivors of childhood acute lymphoblastic leukemia not treated with cranial radiation 496 European ancestry individuals 527 individuals Illumina [> 9000000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST012026 Genome-wide genotyping array 2021-07-13 33048379 Richard MA 2020-10-13 Cancer www.ncbi.nlm.nih.gov/pubmed/33048379 Genetic variation in the body mass index of adult survivors of childhood acute lymphoblastic leukemia: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort. BMI in adult survivors of childhood acute lymphoblastic leukemia 1,458 European ancestry individuals 787 individuals Illumina [> 9000000] (imputed) 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST012028 Genome-wide genotyping array 2020-01-28 31727947 Hoglund J 2019-11-14 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31727947 Improved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers. Inflammatory biomarkers up to 957 Swedish ancestry individuals NA Illumina [12210410] 0 inflammatory biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004872 GCST009522 Genome-wide sequencing 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Uterine fibroids 5,236 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 41 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST009834 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Uterine fibroids (MTAG) 5,236 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 30 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST009833 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Endometriosis 645 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 31 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST009832 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Endometriosis (MTAG) 645 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 15 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST009831 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Ovarian cancer 647 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 37 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST009830 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Ovarian cancer (MTAG) 647 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 22 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST009829 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Endometrial cancer 909 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 12 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST009828 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Endometrial cancer (MTAG) 909 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 9 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST009827 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Gynecologic disease 7,315 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 7 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST009822 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Cervical cancer 538 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 72 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST009826 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Cervical cancer (MTAG) 538 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 62 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST009825 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Gynecologic disease 7,975 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 6 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST009824 Genome-wide genotyping array 2020-04-16 31488892 Masuda T 2019-09-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31488892 GWAS of five gynecologic diseases and cross-trait analysis in Japanese. Gynecologic disease (multivariate analysis) up to 7,975 Japanese ancestry cases, 39,556 Japanese ancestry controls NA Illumina [7645193] (imputed) 15 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST009823 Genome-wide genotyping array 2021-07-27 33393726 Ortiz Fernandez L 2021-01-04 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/33393726 Genetic association of a gain of function interferon gamma receptor 1 (IFNGR1) polymorphism and the intergenic region LNCAROD/DKK1 with Behçet's disease. Behcet's disease 2,344 Turkish ancestry cases, 1,920 Turkish ancestry controls, 437 European ancestry cases, 3,325 European ancestry controls, 312 East Asian ancestry cases, 398 East Asian ancestry controls, 104 Tunisian ancestry cases, 142 Tunisian ancestry controls NA Illumina [up to 1244428] (imputed) 22 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST012073 Genome-wide genotyping array 2019-02-15 30306274 Shah RL 2018-10-10 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30306274 Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. Corneal astigmatism 69,140 European ancestry cases, 17,195 European ancestry controls NA NR [5921785] (imputed) 10 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST007157 Genome-wide genotyping array 2019-02-15 30306274 Shah RL 2018-10-10 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30306274 Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. Refractive astigmatism 70,505 European ancestry cases, 17,500 European ancestry controls NA NR [5919636] (imputed) 10 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST007158 Genome-wide genotyping array 2019-02-15 30306274 Shah RL 2018-10-10 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30306274 Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. Corneal astigmatism Up to 86,335 European ancestry individuals NR [5901671] (imputed) 32 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST007159 Genome-wide genotyping array 2019-02-15 30306274 Shah RL 2018-10-10 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30306274 Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci. Refractive astigmatism 88,005 European ancestry individuals NR [5900115] (imputed) 34 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST007160 Genome-wide genotyping array 2019-03-25 30659259 Imaizumi A 2019-01-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30659259 Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. Plasma free amino acid levels (adjusted for twenty other PFAAs) 1,338 Japanese ancestry individuals NA Illumina [1288202] (imputed) 38 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST007382 Genome-wide genotyping array 2019-03-25 30659259 Imaizumi A 2019-01-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30659259 Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. Plasma free amino acid levels (adjusted for one other PFAA) 1,338 Japanese ancestry individuals NA Illumina [1288202] (imputed) 82 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST007383 Genome-wide genotyping array 2019-03-25 30659259 Imaizumi A 2019-01-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30659259 Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. Plasma free proline levels 1,338 Japanese ancestry individuals 665 Japanese ancestry individuals Illumina [up to 1288202] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST007384 Genome-wide genotyping array 2019-03-25 30659259 Imaizumi A 2019-01-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30659259 Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. Plasma free asparagine levels 1,338 Japanese ancestry individuals 665 Japanese ancestry individuals Illumina [up to 1288202] (imputed) 1 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST007386 Genome-wide genotyping array 2019-03-25 30659259 Imaizumi A 2019-01-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30659259 Genetic basis for plasma amino acid concentrations based on absolute quantification: a genome-wide association study in the Japanese population. Plasma free amino acid levels 1,338 Japanese ancestry individuals NA Illumina [1288202] (imputed) 34 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST007385 Genome-wide genotyping array 2019-09-05 30690781 Pei YF 2019-02-28 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30690781 Joint Association Analysis Identified 18 New Loci for Bone Mineral Density. Total body bone mineral density (MTAG) at least 66,628 individuals NA NR [9704453] 17 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST008603 Genome-wide genotyping array 2019-09-05 30690781 Pei YF 2019-02-28 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30690781 Joint Association Analysis Identified 18 New Loci for Bone Mineral Density. Heel bone mineral density (MTAG) at least 142,487 individuals NA NR [9704453] 17 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST008602 Genome-wide genotyping array 2020-01-23 26567291 Jensen RA 2015-11-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26567291 Novel Genetic Loci Associated With Retinal Microvascular Diameter. Central retinal vein equivalent 14,740 European ancestry individuals, 5,113 Asian ancestry individuals, 3,345 African American individuals, 1,077 Hispanic individuals 5,472 European ancestry individuals Illumina [223566] 4 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009474 Exome genotyping array 2020-01-23 26567291 Jensen RA 2015-11-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26567291 Novel Genetic Loci Associated With Retinal Microvascular Diameter. Central retinal arteriolar equivalent 14,740 European ancestry individuals, 5,113 Asian ancestry individuals, 3,345 African American individuals, 1,077 Hispanic individuals 5,472 European ancestry individuals Illumina [240931] 1 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009475 Exome genotyping array 2021-03-18 31426789 Jeong KH 2019-08-19 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/31426789 Genome-wide association study identifies new susceptible loci of IgA nephropathy in Koreans. IgA nephropathy 188 Korean ancestry cases, 455 Korean ancestry controls 310 Korean ancestry cases, 438 Korean ancestry controls Affymetrix [98667] 0 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST011296 Genome-wide genotyping array 2018-06-21 29747637 Li JQ 2018-05-10 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/29747637 Genome-wide association study identifies two loci influencing plasma neurofilament light levels. Plasma neurofilament light levels 176 European ancestry mild cognitive impairment cases, 172 European ancestry Alzheimer's disease cases, 179 European ancestry controls NA Illumina [301687] 2 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST005713 Genome-wide genotyping array 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Eosinophil counts up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST009041 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Total cholesterol levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 5 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST009042 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. LDL cholesterol levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 5 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST009043 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. HDL cholesterol levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009044 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Triglyceride levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST009045 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Aspartate aminotransferase levels up to 9,004 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST009046 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Alanine aminotransferase levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST009047 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Serum albumin levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST009048 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Serum alkaline phosphatase levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 2 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST009049 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Gamma glutamyl transferase levels up to 9,004 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST009050 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Bilirubin levels 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 2 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST009051 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Diastolic blood pressure 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST009052 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Systolic blood pressure 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST009053 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Hemoglobin A1c levels up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 2 hemoglobin A1 measurement http://www.ebi.ac.uk/efo/EFO_0007629 GCST009054 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Height 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST009055 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Weight 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST009056 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Body mass index 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009057 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Waist circumference 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST009058 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Hip circumference 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST009059 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Waist-hip ratio 14,126 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST009060 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. White blood cell count up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST009061 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Red blood cell count up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST009062 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Mean corpuscular volume up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST009065 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Mean corpuscular hemoglobin up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST009063 Genome-wide genotyping array, Genome-wide sequencing 2019-11-18 31675503 Gurdasani D 2019-10-01 Cell www.ncbi.nlm.nih.gov/pubmed/31675503 Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa. Mean corpuscular hemoglobin concentration up to 7,526 African ancestry individuals NA Affymetrix, Illumina [at least 24423923] (imputed) 1 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST009064 Genome-wide genotyping array, Genome-wide sequencing 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Testosterone levels x fluid intelligence interaction 160,121 British ancestry individuals NA Affymetrix [NR] (imputed) 1 intelligence, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0004908 GCST011153 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Testosterone levels x alcohol consumption (drinks per week) interaction 388,571 British ancestry individuals NA Affymetrix [NR] (imputed) 2 alcohol consumption measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004908 GCST011152 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Testosterone levels x smoking behaviour (cigarettes smoked per day) interaction 414,294 British ancestry individuals NA Affymetrix [NR] (imputed) 2 smoking behaviour measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004908 GCST011151 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Bioavailable testosterone levels x smoking behaviour (cigarettes smoked per day) interaction 414,294 British ancestry individuals NA Affymetrix [NR] (imputed) 0 smoking behaviour measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004908 GCST011150 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Bioavailable testosterone levels x alcohol consumption (drinks per week) interaction 388,571 British ancestry individuals NA Affymetrix [NR] (imputed) 0 alcohol consumption measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004908 GCST011149 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Bioavailable testosterone levels x fluid intelligence interaction 160,121 British ancestry individuals NA Affymetrix [NR] (imputed) 0 intelligence, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0004908 GCST011148 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Estradiol levels x smoking behaviour (cigarettes smoked per day) interaction 185,464 British ancestry men NA Affymetrix [NR] (imputed) 0 smoking behaviour measurement, estradiol measurement http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004697 GCST011147 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Estradiol levels x alcohol consumption (drinks per week) interaction 189,153 British ancestry men NA Affymetrix [NR] (imputed) 0 alcohol consumption measurement, estradiol measurement http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004697 GCST011146 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Estradiol levels x fluid intelligence interaction 73,236 British ancestry men NA Affymetrix [NR] (imputed) 0 intelligence, estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0004697 GCST011145 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Sex hormone-binding globulin levels x smoking behaviour (cigarettes smoked per day) interaction 414,294 British ancestry individuals NA Affymetrix [NR] (imputed) 0 smoking behaviour measurement, sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004696 GCST011144 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Sex hormone-binding globulin levels x alcohol consumption (drinks per week) interaction 388,571 British ancestry individuals NA Affymetrix [NR] (imputed) 0 alcohol consumption measurement, sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004696 GCST011143 Genome-wide genotyping array 2021-02-24 33407712 Liang X 2021-01-06 Mol Brain www.ncbi.nlm.nih.gov/pubmed/33407712 Evaluating the genetic effects of sex hormone traits on the development of mental traits: a polygenic score analysis and gene-environment-wide interaction study in UK Biobank cohort. Sex hormone-binding globulin levels x fluid intelligence interaction 160,121 British ancestry individuals NA Affymetrix [NR] (imputed) 0 intelligence, sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0004696 GCST011142 Genome-wide genotyping array 2019-11-28 31712607 Nudel R 2019-11-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31712607 A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population. Hospital contact for infections 21,728 Danish ancestry cases with psychiatric disorders, 6,744 Danish ancestry cases, 24,161 Danish ancestry controls with psychiatric disorders, 12,901 Danish ancestry controls NA Illumina [11600722] (imputed) 30 susceptibility to infectious disease measurement http://www.ebi.ac.uk/efo/EFO_0008422 GCST009130 Genome-wide genotyping array 2019-12-23 31740837 Lam M 2019-11-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31740837 Comparative genetic architectures of schizophrenia in East Asian and European populations. Schizophrenia 22,778 East Asian ancestry cases, 35,362 East Asian ancestry controls NA Affymetrix, Illumina [9938587] (imputed) 21 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST009336 Genome-wide genotyping array 2019-12-23 31740837 Lam M 2019-11-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31740837 Comparative genetic architectures of schizophrenia in East Asian and European populations. Schizophrenia 22,778 East Asian ancestry cases, 35,362 East Asian ancestry controls, 33,640 European ancestry cases, 43,456 European ancestry controls NA Affymetrix, Illumina [12447948] (imputed) 208 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST009337 Genome-wide genotyping array 2020-02-14 31806883 de Las Fuentes L 2019-12-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/31806883 Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry. LDL cholesterol levels x loop diuretics use interaction 2,117 European ancestry exposed individuals, 30,715 European ancestry unexposed individuals, 784 African American and African ancestry exposed individuals, 5,218 African American and African ancestry unexposed individuals NA Affymetrix, Illumina [NR] (imputed) 4 response to diuretic, low density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0004611 GCST009614 Genome-wide genotyping array 2020-02-14 31806883 de Las Fuentes L 2019-12-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/31806883 Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry. Triglyceride levels x loop diuretics use interaction 2,117 European ancestry exposed individuals, 30,715 European ancestry unexposed individuals, 784 African American and African ancestry exposed individuals, 5,218 African American and African ancestry unexposed individuals NA Affymetrix, Illumina [NR] (imputed) 22 triglyceride measurement, response to diuretic http://www.ebi.ac.uk/efo/EFO_0004530, http://purl.obolibrary.org/obo/GO_0036270 GCST009615 Genome-wide genotyping array 2020-02-14 31806883 de Las Fuentes L 2019-12-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/31806883 Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry. HDL cholesterol levels x thiazide or thiazide-like diuretics use interaction 6,878 European ancestry exposed individuals, 30,715 European ancestry unexposed individuals, 3,923 African American and African ancestry exposed individuals, 5,218 African American and African ancestry unexposed individuals NA Affymetrix, Illumina [NR] (imputed) 6 response to diuretic, high density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0004612 GCST009616 Genome-wide genotyping array 2020-02-14 31806883 de Las Fuentes L 2019-12-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/31806883 Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry. LDL cholesterol levels x thiazide or thiazide-like diuretics use interaction 6,878 European ancestry exposed individuals, 30,715 European ancestry unexposed individuals, 3,923 African American and African ancestry exposed individuals, 5,218 African American and African ancestry unexposed individuals NA Affymetrix, Illumina [NR] (imputed) 2 response to diuretic, low density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0004611 GCST009617 Genome-wide genotyping array 2020-02-14 31806883 de Las Fuentes L 2019-12-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/31806883 Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry. Triglyceride levels x thiazide or thiazide-like diuretics use interaction 6,878 European ancestry exposed individuals, 30,715 European ancestry unexposed individuals, 3,923 African American and African ancestry exposed individuals, 5,218 African American and African ancestry unexposed individuals NA Affymetrix, Illumina [NR] (imputed) 3 triglyceride measurement, response to diuretic http://www.ebi.ac.uk/efo/EFO_0004530, http://purl.obolibrary.org/obo/GO_0036270 GCST009612 Genome-wide genotyping array 2020-02-14 31806883 de Las Fuentes L 2019-12-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/31806883 Genome-wide meta-analysis of variant-by-diuretic interactions as modulators of lipid traits in persons of European and African ancestry. HDL cholesterol levels x loop diuretics use interaction 2,117 European ancestry exposed individuals, 30,715 European ancestry unexposed individuals, 784 African American and African ancestry exposed individuals, 5,218 African American and African ancestry unexposed individuals NA Affymetrix, Illumina [NR] (imputed) 4 response to diuretic, high density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0004612 GCST009613 Genome-wide genotyping array 2020-07-20 32198502 Shin J 2020-03-20 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/32198502 Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes. Cortical surface area (visual PC2) 23,784 European ancestry individuals 19,512 European ancestry individuals, 6,234 individuals Affymetrix, Illumina [NR] (imputed) 30 visual cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0004771 GCST010225 Genome-wide genotyping array 2020-07-20 32198502 Shin J 2020-03-20 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/32198502 Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes. Cortical thickness (PC1) 23,784 European ancestry individuals 19,512 European ancestry individuals, 6,234 individuals Affymetrix, Illumina [NR] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST010224 Genome-wide genotyping array 2020-07-20 32198502 Shin J 2020-03-20 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/32198502 Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes. Cortical thickness (PC2) 23,784 European ancestry individuals 19,512 European ancestry individuals, 6,234 individuals Affymetrix, Illumina [NR] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST010223 Genome-wide genotyping array 2020-07-20 32198502 Shin J 2020-03-20 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/32198502 Global and Regional Development of the Human Cerebral Cortex: Molecular Architecture and Occupational Aptitudes. Cortical surface area (global PC1) 23,784 European ancestry individuals 19,512 European ancestry individuals, 6,234 individuals Affymetrix, Illumina [NR] (imputed) 15 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST010226 Genome-wide genotyping array 2020-06-17 32317632 van de Vegte YJ 2020-04-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32317632 Genome-wide association studies and Mendelian randomization analyses for leisure sedentary behaviours. Leisure sedentary behaviour (television watching) 408,815 European ancestry individuals NA Affymetrix [19400418] (imputed) 157 lifestyle measurement http://www.ebi.ac.uk/efo/EFO_0010724 GCST010084 Genome-wide genotyping array 2020-06-17 32317632 van de Vegte YJ 2020-04-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32317632 Genome-wide association studies and Mendelian randomization analyses for leisure sedentary behaviours. Leisure sedentary behaviour (computer use) 408,815 European ancestry individuals NA Affymetrix [19400418] (imputed) 39 lifestyle measurement http://www.ebi.ac.uk/efo/EFO_0010724 GCST010085 Genome-wide genotyping array 2020-06-17 32317632 van de Vegte YJ 2020-04-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32317632 Genome-wide association studies and Mendelian randomization analyses for leisure sedentary behaviours. Driving (hours per day) 408,815 European ancestry individuals NA Affymetrix [19400418] (imputed) 7 lifestyle measurement http://www.ebi.ac.uk/efo/EFO_0010724 GCST010086 Genome-wide genotyping array 2020-02-13 31873298 Cortes A 2019-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31873298 Identifying cross-disease components of genetic risk across hospital data in the UK Biobank. 19,155 disease classifications in UK Biobank (pleiotropy) 320,644 British ancestry individuals NA Affymetrix [654546] 0 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST009606 Genome-wide genotyping array 2021-07-27 33402679 Lagou V 2021-01-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33402679 Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. Fasting glucose 151,188 European ancestry individuals NA Affymetrix, Illumina [8700000] (imputed) 41 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST012078 Genome-wide genotyping array, Targeted genotyping array 2021-07-27 33402679 Lagou V 2021-01-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33402679 Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. Fasting glucose 67,506 European ancestry men NA Affymetrix, Illumina [8700000] (imputed) 25 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST012077 Genome-wide genotyping array, Targeted genotyping array 2021-07-27 33402679 Lagou V 2021-01-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33402679 Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. Fasting glucose 73,089 European ancestry women NA Affymetrix, Illumina [8700000] (imputed) 27 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST012076 Genome-wide genotyping array, Targeted genotyping array 2021-07-27 33402679 Lagou V 2021-01-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33402679 Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. Fasting insulin 105,056 European ancestry individuals NA Affymetrix, Illumina [8700000] (imputed) 17 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST012079 Genome-wide genotyping array, Targeted genotyping array 2021-07-27 33402679 Lagou V 2021-01-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33402679 Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. Fasting insulin 47,806 European ancestry men NA Affymetrix, Illumina [8700000] (imputed) 8 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST012075 Genome-wide genotyping array, Targeted genotyping array 2021-07-27 33402679 Lagou V 2021-01-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33402679 Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability. Fasting insulin 50,404 European ancestry women NA Affymetrix, Illumina [8700000] (imputed) 7 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST012074 Genome-wide genotyping array, Targeted genotyping array 2020-05-09 22936693 Juran BD 2012-08-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22936693 Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. Primary biliary cirrhosis 2,216 European ancestry cases, 5,594 Europen ancestry controls NA Illumina [109812] 24 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST009956 Targeted genotyping array [ImmunoChip] 2020-10-15 31985465 Chen SD 2020-01-20 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/31985465 Genome-Wide Association Study Identifies SLAMF1 Affecting the Rate of Memory Decline. Memory decline 709 European ancestry individuals NA Illumina [1197412] 3 cognitive decline measurement, memory performance http://www.ebi.ac.uk/efo/EFO_0007710, http://www.ebi.ac.uk/efo/EFO_0004874 GCST010679 Genome-wide genotyping array 2020-07-21 32222710 Hosgood Iii HD 2020-03-27 Respiration www.ncbi.nlm.nih.gov/pubmed/32222710 PRDM15 Is Associated with Risk of Chronic Obstructive Pulmonary Disease in a Rural Population in Chile. Chronic obstructive pulmonary disease 214 Chilean cases, 193 Chilean controls NA Illumina [455564] (imputed) 5 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST010249 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Systolic blood pressure 6,254 European ancestry individuals NA NR [~ 24000000] (imputed) 1 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST010259 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Diastolic blood pressure 6,253 European ancestry individuals NA NR [~ 24000000] (imputed) 3 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST010258 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Diastolic blood pressure x quantitative lifestyle risk score interaction (1df test) 6,253 European ancestry individuals NA NR [2411113] (imputed) 2 lifestyle measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006336 GCST010257 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Diastolic blood pressure x quantitative lifestyle risk score interaction (2df test) 6,253 European ancestry individuals NA NR [2411113] (imputed) 3 lifestyle measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006336 GCST010256 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Diastolic blood pressure x dichotomous lifestyle risk score interaction (1df test) 1,924 European ancestry unexposed individuals, 4,330 European ancestry exposed individuals NA NR [2407627] (imputed) 2 lifestyle measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006336 GCST010255 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Diastolic blood pressure x dichotomous lifestyle risk score interaction (2df test) 1,924 European ancestry unexposed individuals, 4,330 European ancestry exposed individuals NA NR [2407627] (imputed) 2 lifestyle measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006336 GCST010254 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Systolic blood pressure x quantitative lifestyle risk score interaction (1df test) 6,254 European ancestry individuals NA NR [2411114] (imputed) 3 lifestyle measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006335 GCST010253 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Systolic blood pressure x quantitative lifestyle risk score interaction (2df test) 6,254 European ancestry individuals NA NR [2411114] (imputed) 4 lifestyle measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006335 GCST010252 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Systolic blood pressure x dichotomous lifestyle risk score interaction (1df test) 1,924 European ancestry unexposed individuals, 4,330 European ancestry exposed individuals NA NR [2407629] (imputed) 2 lifestyle measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006335 GCST010251 Genome-wide genotyping array 2020-07-21 32227373 Osazuwa-Peters OL 2020-03-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32227373 Identifying blood pressure loci whose effects are modulated by multiple lifestyle exposures. Systolic blood pressure x dichotomous lifestyle risk score interaction (2df test) 1,924 European ancestry unexposed individuals, 4,330 European ancestry exposed individuals NA NR [2407629] (imputed) 3 lifestyle measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0006335 GCST010250 Genome-wide genotyping array 2019-04-30 25043022 Moltke I 2014-06-18 Nature www.ncbi.nlm.nih.gov/pubmed/25043022 A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes. Two-hour insulin response 2,540 Greenlandic ancestry individuals 845 Greenlandic ancestry individuals Illumina [up to 196725] 0 insulin response measurement http://www.ebi.ac.uk/efo/EFO_0008473 GCST007669 Targeted genotyping array [Cardio-MetaboChip] 2019-04-30 25043022 Moltke I 2014-06-18 Nature www.ncbi.nlm.nih.gov/pubmed/25043022 A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes. Fasting blood glucose 2,575 Greenlandic ancestry individuals 1,064 Greenlandic ancestry individuals Illumina [up to 196725] 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007670 Targeted genotyping array [Cardio-MetaboChip] 2019-04-30 25043022 Moltke I 2014-06-18 Nature www.ncbi.nlm.nih.gov/pubmed/25043022 A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes. Fasting blood insulin 2,575 Greenlandic ancestry individuals 1,062 Greenlandic ancestry individuals Illumina [up to 196725] 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007671 Targeted genotyping array [Cardio-MetaboChip] 2019-04-30 25043022 Moltke I 2014-06-18 Nature www.ncbi.nlm.nih.gov/pubmed/25043022 A common Greenlandic TBC1D4 variant confers muscle insulin resistance and type 2 diabetes. Two-hour glucose 2,540 Greenlandic ancestry individuals 845 Greenlandic ancestry individuals Illumina [up to 196725] 1 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST007668 Targeted genotyping array [Cardio-MetaboChip] 2020-07-09 32157568 Strupp M 2020-03-10 Cerebellum www.ncbi.nlm.nih.gov/pubmed/32157568 A Variation in FGF14 Is Associated with Downbeat Nystagmus in a Genome-Wide Association Study. Idiopathic downbeat nystagmus 106 European ancestry cases, 2,609 European ancestry controls NA Illumina [7759885] (imputed) 16 Nystagmus http://purl.obolibrary.org/obo/HP_0000639 GCST010172 Genome-wide genotyping array 2019-08-23 31434886 Luo Y 2019-08-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31434886 Early progression to active tuberculosis is a highly heritable trait driven by 3q23 in Peruvians. Early progression to active pulmonary tuberculosis in Mycobacterium tuberculosis-infected individuals 2,160 Peruvian cases, 1,820 Peruvian controls NA Affymetrix [7756401] (imputed) 1 susceptibility to Mycobacterium tuberculosis infection measurement, tuberculosis http://www.ebi.ac.uk/efo/EFO_0008407, http://purl.obolibrary.org/obo/MONDO_0018076 GCST008488 Genome-wide genotyping array 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (very severe respiratory confirmed vs not hospitalized) RELEASE 4 269 European ancestry cases, 688 European ancestry controls NA Affymetrix, Illumina [9309252] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010775 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (covid vs lab/self reported negative) RELEASE 4 8,818 Europen ancestry cases, 101,806 European ancestry controls, 114 South Asian ancestry cases, 256 South Asian ancestry controls, 63 African ancestry cases, 125 African ancestry controls, 66 Central/South Asian ancestry cases, 350 Central/South Asian ancestry controls, 576 Latin American cases, 3,601 Latin American controls NA Affymetrix, Illumina [22039729] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010778 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (RELEASE 5) 31,562 European ancestry cases, 1,026,848 European ancestry controls, 2,619 Latin American cases, 15,491 Latin American controls, 1,495 East Asian ancestry cases, 15,499 East Asian ancestry controls, 1,379 South Asian ancestry cases, 32,785 South Asian ancestry controls, 2,338 African ancestry cases, 23,485 African ancestry controls, 700 Arab ancestry cases, 13,360 Arab ancestry controls, 1,022 Admixed American ancestry cases, 5,330 Admixed American ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011072 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (RELEASE 5) 38,984 European ancestry cases, 1,644,784 European ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011073 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (RELEASE 5) 32,494 European ancestry cases, 1,316,207 European ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011074 Genome-wide genotyping array, Exome-wide sequencing, Genome-wide sequencing 2020-07-13 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (very severe respiratory confirmed vs population) RELEASE 3 435 European ancestry cases, 327,858 European ancestry controls, 101 Latin American cases, 1,533 Latin American controls NA Affymetrix, Illumina [9309252] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010198 Genome-wide genotyping array, Exome-wide sequencing, Genome-wide sequencing 2020-07-13 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs not hospitalized) RELEASE 3 928 European ancestry cases, 2,028 European ancestry controls NA Affymetrix, Illumina [12029424] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010199 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-07-13 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs population) RELEASE 3 2,961 European ancestry hospitalized cases, 868,602 European ancestry controls, 176 Latin American hospitalized cases, 1,533 Latin American controls, 62 South Asian ancestry hospitalized cases, 27,353 South Asian ancestry controls NA Affymetrix, Illumina [15392647] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010200 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-07-13 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (covid vs lab/self reported negative) RELEASE 3 3,289 Europen ancestry cases, 36,125 European ancestry controls, 114 South Asian ancestry cases, 256 South Asian ancestry controls, 63 African ancestry cases, 125 African ancestry controls, 57 Central/South Asian ancestry cases, 128 Central/South Asian ancestry controls NA Affymetrix, Illumina [22039729] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010201 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-07-13 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (RELEASE 3) 6,089 European ancestry cases, 1,015,145 European ancestry controls, 197 Arab ancestry cases, 13,698 Arab ancestry cases, 176 Latin American cases, 1,533 Latin American controls, 114 South Asian ancestry cases, 27,301 South Asian ancestry controls, 63 African ancestry cases, 6,573 African ancestry controls, 57 Central/South Asian ancestry cases, 8,819 Central/South Asian ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010202 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-07-13 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (predicted from self-reported symptoms vs predicted or self-reported non-covid) RELEASE 3 1,865 European ancestry cases, 29,174 European ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010203 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (very severe respiratory confirmed vs population) RELEASE 5 5,101 European ancestry cases, 1,383,241 European ancestry controls NA Affymetrix, Illumina [9309252] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011075 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (very severe respiratory confirmed vs population) RELEASE 5 4,606 European ancestry cases, 702,801 European ancestry controls, 539 Latin American cases, 1,149 Latin American controls, 133 African American cases, 2,610 African American controls, 304 East Asian ancestry cases, 2,450 East Asian ancestry controls NA Affymetrix, Illumina [9309252] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011076 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (very severe respiratory confirmed vs population) RELEASE 5 4,792 European ancestry cases, 1,054,664 European ancestry controls, 641 Latin American cases, 96,479 Latin American controls, 133 African American cases, 2,610 African American controls, 304 East Asian ancestry cases, 2,450 East Asian ancestry controls NA Affymetrix, Illumina [9309252] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011077 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (very severe respiratory confirmed vs population) RELEASE 5 4,792 European ancestry cases, 1,054,664 European ancestry controls NA Affymetrix, Illumina [9309252] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011078 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs not hospitalized) RELEASE 5 3,159 European ancestry cases, 7,206 European ancestry controls NA Affymetrix, Illumina [12029424] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011079 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs not hospitalized) RELEASE 5 4,829 European ancestry cases, 11,816 European ancestry controls NA Affymetrix, Illumina [12029424] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011080 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs population) RELEASE 5 9,986 European ancestry cases, 1,877,672 European ancestry controls NA Affymetrix, Illumina [15392647] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011081 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs population) RELEASE 5 8,316 European ancestry cases, 1,549,095 European ancestry controls, 257 Latin American cases, 94,912 Latin American controls, 115 South Asian ancestry cases, 34,049 South Asian ancestry controls, 60 Arab ancestry cases, 13,360 Arab ancestry controls, 653 African ancestry cases, 4,355 African ancestry controls, 1,414 East Asian ancestry cases, 15,499 East Asian ancestry controls, 948 Admixed American ancestry cases, 5,404 Admixed American ancestry controls NA Affymetrix, Illumina [15392647] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011082 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs population) RELEASE 5 8,316 European ancestry cases, 1,549,095 European ancestry controls NA Affymetrix, Illumina [15392647] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011083 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs population) RELEASE 5 9,373 European ancestry cases, 1,197,256 European ancestry controls, 117 Latin American cases, 585 Latin American controls, 186 South Asian ancestry cases, 43,280 South Asian ancestry controls, 60 Arab ancestry cases, 13,360 Arab ancestry controls, 790 African ancestry cases, 20,582 African ancestry controls, 1,414 East Asian ancestry cases, 15,499 East Asian ancestry controls, 948 Admixed American ancestry cases, 5,404 Admixed American ancestry controls NA Affymetrix, Illumina [15392647] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011084 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (RELEASE 4) 14,134 European ancestry cases, 1,284,876 European ancestry controls, 1,332 Latin American cases, 6,592 Latin American controls, 66 Central Asian ancestry cases, 8,487 Central Asian ancestry controls, 108 East Asian ancestry cases, 6,500 East Asian ancestry controls, 114 South Asian ancestry cases, 27,301 South Asian ancestry controls, 1,511 African ancestry cases, 23,431 African ancestry controls, 700 Arab ancestry cases, 13,360 Arab ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010780 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (very severe respiratory confirmed vs population) RELEASE 4 3,886 European ancestry cases, 622,265 European ancestry controls, 450 Latin American cases, 1,637 Latin American controls NA Affymetrix, Illumina [9309252] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010783 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized covid vs not hospitalized) RELEASE 4 1,776 European ancestry cases, 6,443 European ancestry controls, 62 South Asian ancestry cases, 41 South Asian ancestry controls, 415 African ancestry cases, 962 African ancestry controls, 60 Arab ancestry cases, 640 Arab ancestry controls, 117 Hispanic cases, 392 Hispanic controls NA Affymetrix, Illumina [12029424] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010782 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (predicted covid from self-reported symptoms vs predicted or self-reported non-covid) RELEASE 4 3,204 European ancestry cases, 35,728 European ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010781 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-06-25 32358547 Persyn E 2020-05-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32358547 Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants. White matter hyperintensities 39,011 European ancestry individuals, 2,099 African ancestry individuals, 795 Hispanic individuals, 3,299 Asian ancestry individuals NA Affymetrix [9700000] (imputed) 19 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST010101 Genome-wide genotyping array 2020-06-25 32358547 Persyn E 2020-05-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32358547 Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants. White matter integrity (fractional anisotropy) 17,663 European ancestry individuals NA Affymetrix [NR] (imputed) 9 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST010102 Genome-wide genotyping array 2020-06-25 32358547 Persyn E 2020-05-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32358547 Genome-wide association study of MRI markers of cerebral small vessel disease in 42,310 participants. White matter integrity (mean diffusivity) 17,467 European ancestry individuals NA Affymetrix [NR] (imputed) 6 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST010103 Genome-wide genotyping array 2021-01-05 30679421 Felsky D 2019-01-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30679421 Neuropathological correlates and genetic architecture of microglial activation in elderly human brain. Proportion of activated microglia (midfrontal cortex) 225 individuals NA NR [NR] (imputed) 12 microglial activation measurement http://www.ebi.ac.uk/efo/EFO_0010940 GCST010917 Genome-wide genotyping array 2021-01-05 30679421 Felsky D 2019-01-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30679421 Neuropathological correlates and genetic architecture of microglial activation in elderly human brain. Proportion of activated microglia (inferior temporal cortex) 219 individuals NA NR [NR] (imputed) 26 microglial activation measurement http://www.ebi.ac.uk/efo/EFO_0010940 GCST010916 Genome-wide genotyping array 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs population) RELEASE 4 6,406 European ancestry hospitalized cases, 902,088 European ancestry controls, 873 Latin American hospitalized cases, 2,222 Latin American controls, 62 South Asian ancestry hospitalized cases, 27,353 South Asian ancestry controls, 60 Arab ancestry hospitalized cases, 13,360 Arab ancestry controls, 415 African ancestry hospitalized cases, 10,281 African ancestry controls, 69 East Asian ancestry hospitalized cases, 6,500 East Asian ancestry controls NA Affymetrix, Illumina [15392647] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010779 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (RELEASE 5) 29,071 European ancestry cases, 1,559,712 European ancestry controls, 576 Latin American cases, 4,955 Latin American controls, 1,495 East Asian ancestry cases, 15,499 East Asian ancestry controls, 1,688 South Asian ancestry cases, 42,016 South Asian ancestry controls, 2,038 African ancestry cases, 28,066 African ancestry controls, 700 Arab ancestry cases, 13,360 Arab ancestry controls, 1,022 Admixed American ancestry cases, 5,330 Admixed American ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011071 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs not hospitalized) RELEASE 5 4,829 European ancestry cases, 11,816 European ancestry controls, 186 South Asian ancestry cases, 1,494 South Asian ancestry controls, 486 African ancestry cases, 1,081 African ancestry controls, 60 Arab ancestry cases, 640 Arab ancestry controls, 117 Hispanic cases, 392 Hispanic controls, 95 Admixed American ancestry cases, 75 Admixed American ancestry controls NA Affymetrix, Illumina [12029424] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011086 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-02-04 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs not hospitalized) RELEASE 5 3,159 European ancestry cases, 7,206 European ancestry controls, 115 South Asian ancestry cases, 1,264 South Asian ancestry controls, 415 African ancestry cases, 962 African ancestry controls, 60 Arab ancestry cases, 640 Arab ancestry controls, 117 Hispanic cases, 392 Hispanic controls, 95 Admixed American ancestry cases, 74 Admixed American ancestry controls NA Affymetrix, Illumina [12029424] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST011085 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (hospitalized vs population) RELEASE 4 6,406 European ancestry cases, 902,088 European ancestry controls NA Affymetrix, Illumina [15392647] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010777 Genome-wide genotyping array, Exome-wide sequencing, Genome-wide sequencing 2020-11-27 32404885 COVID-19 Host Genetics Initiative 2020-05-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32404885 The COVID-19 Host Genetics Initiative, a global initiative to elucidate the role of host genetic factors in susceptibility and severity of the SARS-CoV-2 virus pandemic. COVID-19 (RELEASE 4) 14,134 European ancestry cases, 1,284,876 European ancestry controls NA Affymetrix, Illumina [24600933] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST010776 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Sclerostin levels 1,312 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010348 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Scavenger receptor cysteine-rich domain-containing group B protein levels 1,272 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010349 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Sulfatase-modifying factor 2 levels 1,312 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010350 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Trefoil factor 2 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010351 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Thimet oligopeptidase levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010352 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Thyrotropin subunit beta levels 1,285 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010353 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Thioredoxin domain-containing protein 5 levels 1,309 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010354 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Thymidine phosphorylase levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010355 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Tyrosine-protein kinase receptor TYRO3 levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010356 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Ubiquitin carboxyl-terminal hydrolase 8 levels 1,138 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010357 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Versican core protein levels 1,313 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010358 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Angiotensin-converting enzyme 2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010102 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. A disintegrin and metalloproteinase with thrombospondin motifs 13 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010103 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Agouti-related protein levels 1,300 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010104 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Protein AMBP levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010105 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Angiopoietin-1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010106 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Bone morphogenetic protein 6 levels 1,214 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010107 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Brother of CDO levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010108 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Carbonic anhydrase 5A,mitochondrial levels 1,263 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010109 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-C motif chemokine 17 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010110 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-C motif chemokine 3 levels 1,288 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010111 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. T-cell surface glycoprotein CD4 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010112 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. CD40 ligand levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010113 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. SLAM family member 5 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010114 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Carcinoembryonic antigenrelated cell adhesion molecule 8 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010115 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Chymotrypsin C levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010116 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Cathepsin L1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010117 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. C-X-C motif chemokine 1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010118 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Decorin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010119 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. 2,4-dienoyl-CoA reductase,mitochondrial levels 1,296 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010120 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Dickkopf-related protein 1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010121 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Fatty acid-binding protein,intestinal levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010122 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Fibroblast growth factor 21 levels 1,298 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010123 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Fibroblast growth factor 23 levels 1,286 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010124 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Follistatin levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010125 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Galectin-9 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010126 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Growth/differentiation factor 2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010127 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Growth hormone levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010128 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Gastric intrinsic factor levels 1,299 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010129 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Lactoylglutathione lyase levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010130 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Gastrotropin levels 1,047 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010131 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Hydroxyacid oxidase 1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010132 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Proheparin-binding EGF-like growth factor levels 1,300 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010133 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Heme oxygenase 1 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010134 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Osteoclast-associated immunoglobulin-like receptor levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010135 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Heat shock 27 kDa protein levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010136 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Alpha-L-iduronidase levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010137 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Low affinity immunoglobulin gamma Fc region receptor II-b levels 1,295 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010138 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Pro-interleukin-16 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010139 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-17D levels 1,299 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010140 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-18 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010141 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-1-receptor antagonist levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010142 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-1 receptor-like 2 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010143 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-27 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010144 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-4 receptor subunit alpha levels 1,292 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010145 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Interleukin-6 levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010146 Genome-wide sequencing [22x] 2021-01-20 33303764 Gilly A 2020-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33303764 Whole-genome sequencing analysis of the cardiometabolic proteome. Kidney Injury Molecule levels 1,301 European ancestry individuals NA Illumina [13419876] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90010147 Genome-wide sequencing [22x] 2020-02-14 31815349 Chen VL 2019-12-09 Liver Int www.ncbi.nlm.nih.gov/pubmed/31815349 Genetic variants that associate with liver cirrhosis have pleiotropic effects on human traits. Cirrhosis 1,088 British ancestry cases, 407,873 British ancestry controls 875 European ancestry cases, 30,346 European ancestry controls Affymetrix [18530078] (imputed) 1 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST009609 Genome-wide genotyping array 2020-10-15 31982041 Guillen-Guio B 2020-01-23 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31982041 Sepsis-associated acute respiratory distress syndrome in individuals of European ancestry: a genome-wide association study. Acute respiratory distress syndrome in sepsis 274 European ancestry cases, 316 European ancestry controls 359 European ancestry cases, 986 European ancestry controls Affymetrix [7984208] (imputed) 2 acute respiratory distress syndrome http://www.ebi.ac.uk/efo/EFO_1000637 GCST010680 Genome-wide genotyping array 2022-09-21 31999318 Simcoe MJ 2020-01-30 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31999318 Genetic Heritability of Pigmentary Glaucoma and Associations With Other Eye Phenotypes. Pigmentary glaucoma 227 European ancestry cases, 291 European ancestry controls NA Illumina [NR] (imputed) 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST012959 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Occipital lobe volume 15,269 European ancestry individuals 8,789 European ancestry individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 2 occipital lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010145 GCST008703 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Parietal lobe volume 15,269 European ancestry individuals 8,789 European ancestry individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 0 parietal lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010146 GCST008704 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Temporal lobe volume 15,269 European ancestry individuals 8,789 European ancestry individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 0 temporal lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010147 GCST008705 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Occipital lobe volume 15,269 European ancestry individuals, 405 African American individuals, 211 Chinese ancestry individuals, 131 Malay ancestry individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 4 occipital lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010145 GCST008707 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Parietal lobe volume 15,269 European ancestry individuals, 405 African American individuals, 211 Chinese ancestry individuals, 131 Malay ancestry individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 2 parietal lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010146 GCST008710 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Temporal lobe volume 15,269 European ancestry individuals, 405 African American individuals, 211 Chinese ancestry individuals, 131 Malay ancestry individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 1 temporal lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010147 GCST008711 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Frontal lobe volume 15,269 European ancestry individuals 8,789 European ancestry individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 0 frontal lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010144 GCST008715 Genome-wide genotyping array 2019-09-20 31396565 van der Lee SJ 2019-08-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31396565 A genome-wide association study identifies genetic loci associated with specific lobar brain volumes. Frontal lobe volume 15,269 European ancestry individuals, 405 African American individuals, 211 Chinese ancestry individuals, 131 Malay ancestry individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 0 frontal lobe volume measurement http://www.ebi.ac.uk/efo/EFO_0010144 GCST008717 Genome-wide genotyping array 2020-07-21 32239398 Liu L 2020-04-01 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32239398 Two novel pleiotropic loci associated with osteoporosis and abdominal obesity. Femoral neck bone mineral density 10,208 European ancestry individuals, 445 Hispanic individuals, 843 African ancestry individuals, 1,539 East Asian individuals NA Affymetrix, Illumina [12061510] (imputed) 8 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST010268 Genome-wide genotyping array 2020-07-21 32239398 Liu L 2020-04-01 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32239398 Two novel pleiotropic loci associated with osteoporosis and abdominal obesity. Trunk fat mass adjusted for trunk lean mass 10,208 European ancestry individuals, 445 Hispanic individuals, 843 African ancestry individuals, 1,539 East Asian individuals NA Affymetrix, Illumina [12061510] (imputed) 9 lean mass-adjusted fat body mass http://www.ebi.ac.uk/efo/EFO_0009890 GCST010267 Genome-wide genotyping array 2020-07-21 32239398 Liu L 2020-04-01 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32239398 Two novel pleiotropic loci associated with osteoporosis and abdominal obesity. Femoral neck bone mineral density and trunk fat mass adjusted by trunk lean mass 10,208 European ancestry individuals, 445 Hispanic individuals, 843 African ancestry individuals, 1,539 East Asian individuals NA Affymetrix, Illumina [12061510] (imputed) 18 lean mass-adjusted fat body mass, femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0009890, http://www.ebi.ac.uk/efo/EFO_0007785 GCST010266 Genome-wide genotyping array 2020-07-21 32239439 Barr PB 2020-04-01 Behav Genet www.ncbi.nlm.nih.gov/pubmed/32239439 A Family-Based Genome Wide Association Study of Externalizing Behaviors. Externalizing behaviour score 7,568 European ancestry individuals, 3,274 African ancestry individuals, 4,270 European and African ancestry individuals NA Affymetrix, Illumina [up to 15537641] (imputed) 5 substance abuse, antisocial behaviour measurement http://purl.obolibrary.org/obo/MONDO_0002491, http://www.ebi.ac.uk/efo/EFO_0007052 GCST010280 Genome-wide genotyping array 2020-02-06 31289819 Fitzgerald KC 2019-09-01 Brain www.ncbi.nlm.nih.gov/pubmed/31289819 Early complement genes are associated with visual system degeneration in multiple sclerosis. Decreased low contrast letter acuity in multiple sclerosis 582 European and unknown ancestry individuals 253 European and unknown ancestry individuals Illumina [5258576] (imputed) 6 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST009560 Genome-wide genotyping array 2020-02-06 31289819 Fitzgerald KC 2019-09-01 Brain www.ncbi.nlm.nih.gov/pubmed/31289819 Early complement genes are associated with visual system degeneration in multiple sclerosis. Rate of retinal ganglion cell–inner plexiform layer atrophy in multiple sclerosis 374 European and unknown ancestry individuals 376 individuals Illumina [503678] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST009559 Genome-wide genotyping array 2020-02-13 31760383 Guo Y 2019-11-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/31760383 Genome-wide association study of hippocampal atrophy rate in non-demented elders. Hippocampal atrophy rate 602 European ancestry elderly individuals NA Illumina [695203] 3 hippocampal atrophy http://www.ebi.ac.uk/efo/EFO_0005039 GCST009608 Genome-wide genotyping array 2020-02-27 31170332 Zheng J 2019-08-02 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/31170332 Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures. Serum sclerostin levels 10,584 European ancestry individuals NA NR [5245208] (imputed) 3 sclerostin measurement http://www.ebi.ac.uk/efo/EFO_0010606 GCST009708 Genome-wide genotyping array 2020-07-08 32059762 Manousaki D 2020-02-05 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32059762 Genome-wide Association Study for Vitamin D Levels Reveals 69 Independent Loci. Serum 25-Hydroxyvitamin D levels 443,734 European ancestry individuals NA Affymetrix [16668957] (imputed) 138 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST010144 Genome-wide genotyping array 2019-03-12 30670697 Kilpelainen TO 2019-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30670697 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. HDL cholesterol x physical activity interaction (2df test) 7,395 African American inactive individuals, 13,092 African American active individuals, 2,753 Asian ancestry inactive individuals, 3,650 Asian ancestry active individuals, 22,963 European ancestry inactive individuals, 61,939 European ancestry active individuals, 2,829 Hispanic or Latin American inactive individuals, 6,358 Hispanic or Latin American active individuals 1,886 African American inactive individuals, 1,892 African American active individuals, 1,217 South African Black ancestry inactive individuals, 389 South African Black ancestry active individuals, 2,494 East Asian ancestry inactive individuals, 1,947 East Asian ancestry active individuals, 724 South Asian ancestry inactive individuals, 1,425 South Asian ancestry active individuals, 41,042 European ancestry inactive individuals, 66,575 European ancestry active individuals, 2,619 Hispanic inactive individuals, 8,802 Hispanic active individuals Affymetrix, Illumina [at least 2500000] (imputed) 42 HDL cholesterol change measurement, physical activity http://www.ebi.ac.uk/efo/EFO_0007805, http://www.ebi.ac.uk/efo/EFO_0003940 GCST007282 Genome-wide genotyping array 2019-03-12 30670697 Kilpelainen TO 2019-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30670697 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. LDL cholesterol x physical activity interaction (2df test) 7,260 African American inactive individuals, 12,761 African American active individuals, 2,740 Asian ancestry inactive individuals, 3,615 Asian ancestry active individuals, 22,378 European ancestry inactive individuals, 55,310 European ancestry active individuals, 2,163 Hispanic or Latin American inactive individuals, 3,461 Hispanic or Latin American active individuals 571 African American inactive individuals, 1,521 African American active individuals, 1,217 South African Black ancestry inactive individuals, 389 South African Black ancestry active individuals, 2,495 East Asian ancestry inactive individuals, 1,947 East Asian ancestry active individuals, 724 South Asian ancestry inactive individuals, 1,425 South Asian ancestry active individuals, 33,796 European ancestry inactive individuals, 50,812 European ancestry active individuals, 2,578 Hispanic inactive individuals, 8,661 Hispanic active individuals Affymetrix, Illumina [at least 2500000] (imputed) 39 low density lipoprotein cholesterol measurement, physical activity http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0003940 GCST007284 Genome-wide genotyping array 2019-03-12 30670697 Kilpelainen TO 2019-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30670697 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Triglycerides x physical activity interaction (2df test) 7,294 African American inactive individuals, 12,832 African American active individuals, 1,352 Asian ancestry inactive individuals, 3,049 Asian ancestry active individuals, 20,622 European ancestry inactive individuals, 51,480 European ancestry active individuals, 2,166 Hispanic or Latin American inactive individuals, 3,486 Hispanic or Latin American active individuals 580 African American inactive individuals, 1,540 African American active individuals, 1,217 South African Black ancestry inactive individuals, 389 South African Black ancestry active individuals, 765 East Asian ancestry inactive individuals, 1,814 East Asian ancestry active individuals, 724 South Asian ancestry inactive individuals, 1,424 South Asian ancestry active individuals, 32,456 European ancestry inactive individuals, 49,510 European ancestry active individuals, 2,619 Hispanic inactive individuals, 8,803 Hispanic active individuals Affymetrix, Illumina [at least 2500000] (imputed) 24 triglyceride measurement, physical activity http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0003940 GCST007286 Genome-wide genotyping array 2019-03-12 30670697 Kilpelainen TO 2019-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30670697 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. LDL cholesterol x physical activity interaction (1df test) 7,260 African American inactive individuals, 12,761 African American active individuals, 2,740 Asian ancestry inactive individuals, 3,615 Asian ancestry active individuals, 22,378 European ancestry inactive individuals, 55,310 European ancestry active individuals, 2,163 Hispanic or Latin American inactive individuals, 3,461 Hispanic or Latin American active individuals 571 African American inactive individuals, 1,521 African American active individuals, 1,217 South African Black ancestry inactive individuals, 389 South African Black ancestry active individuals, 2,495 East Asian ancestry inactive individuals, 1,947 East Asian ancestry active individuals, 724 South Asian ancestry inactive individuals, 1,425 South Asian ancestry active individuals, 33,796 European ancestry inactive individuals, 50,812 European ancestry active individuals, 2,578 Hispanic inactive individuals, 8,661 Hispanic active individuals Affymetrix, Illumina [at least 2500000] (imputed) 1 low density lipoprotein cholesterol measurement, physical activity http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0003940 GCST007283 Genome-wide genotyping array 2019-03-12 30670697 Kilpelainen TO 2019-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30670697 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. HDL cholesterol x physical activity interaction (1df test) 7,395 African American inactive individuals, 13,092 African American active individuals, 2,753 Asian ancestry inactive individuals, 3,650 Asian ancestry active individuals, 22,963 European ancestry inactive individuals, 61,939 European ancestry active individuals, 2,829 Hispanic or Latin American inactive individuals, 6,358 Hispanic or Latin American active individuals 1,886 African American inactive individuals, 1,892 African American active individuals, 1,217 South African Black ancestry inactive individuals, 389 South African Black ancestry active individuals, 2,494 East Asian ancestry inactive individuals, 1,947 East Asian ancestry active individuals, 724 South Asian ancestry inactive individuals, 1,425 South Asian ancestry active individuals, 41,042 European ancestry inactive individuals, 66,575 European ancestry active individuals, 2,619 Hispanic inactive individuals, 8,802 Hispanic active individuals Affymetrix, Illumina [at least 2500000] (imputed) 3 physical activity, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0003940, http://www.ebi.ac.uk/efo/EFO_0004612 GCST007281 Genome-wide genotyping array 2019-03-12 30670697 Kilpelainen TO 2019-01-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30670697 Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity. Triglycerides x physical activity interaction (1df test) 7,294 African American inactive individuals, 12,832 African American active individuals, 1,352 Asian ancestry inactive individuals, 3,049 Asian ancestry active individuals, 20,622 European ancestry inactive individuals, 51,480 European ancestry active individuals, 2,166 Hispanic or Latin American inactive individuals, 3,486 Hispanic or Latin American active individuals 580 African American inactive individuals, 1,540 African American active individuals, 1,217 South African Black ancestry inactive individuals, 389 South African Black ancestry active individuals, 765 East Asian ancestry inactive individuals, 1,814 East Asian ancestry active individuals, 724 South Asian ancestry inactive individuals, 1,424 South Asian ancestry active individuals, 32,456 European ancestry inactive individuals, 49,510 European ancestry active individuals, 2,619 Hispanic inactive individuals, 8,803 Hispanic active individuals Affymetrix, Illumina [at least 2500000] (imputed) 0 triglyceride measurement, physical activity http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0003940 GCST007285 Genome-wide genotyping array 2020-07-23 32341527 Landi MT 2020-04-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32341527 Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Cutaneous malignant melanoma 36,760 European ancestry cases, 375,188 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 76 cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0000389 GCST010304 Genome-wide genotyping array 2020-07-23 32341527 Landi MT 2020-04-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32341527 Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Cutaneous melanoma or hair colour 36,760 European ancestry cutaneous melanoma cases, 375,188 European ancestry controls, 352,662 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 48 cutaneous melanoma, hair color http://www.ebi.ac.uk/efo/EFO_0000389, http://www.ebi.ac.uk/efo/EFO_0003924 GCST010302 Genome-wide genotyping array 2020-07-23 32341527 Landi MT 2020-04-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32341527 Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Nevus count or cutaneous melanoma 36,760 European ancestry cutaneous melanoma cases, 375,188 European ancestry controls, 12,930 European ancestry individuals, 52,847 individuals NA Affymetrix, Illumina [NR] (imputed) 66 nevus count, cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0004632, http://www.ebi.ac.uk/efo/EFO_0000389 GCST010303 Genome-wide genotyping array 2021-05-19 33082346 Xu K 2020-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33082346 Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. Smoking status (current vs mixed) 40,456 European ancestry current smokers, 13,511 African American current smokers, 2,920 Hispanic current smokers, 110,403 European ancestry mixed smokers, 23,605 African American mixed smokers, 11,221 Hispanic mixed smokers NA Affymetrix [~ 79000000] (imputed) 5 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST011701 Genome-wide genotyping array 2021-05-19 33082346 Xu K 2020-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33082346 Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. Smoking initiation 842,717 European ancestry individuals NA Affymetrix [up to 79000000] (imputed) 99 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST011703 Genome-wide genotyping array 2021-05-19 33082346 Xu K 2020-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33082346 Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. Smoking cessation 450,129 European ancestry individuals NA Affymetrix [up to 79000000] (imputed) 13 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST011702 Genome-wide genotyping array 2021-05-19 33082346 Xu K 2020-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33082346 Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. Cigarettes smoked per day (current) 17,014 European ancestry individuals NA Affymetrix [~ 79000000] (imputed) 3 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST011700 Genome-wide genotyping array 2021-05-19 33082346 Xu K 2020-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33082346 Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. Cigarettes smoked per day (past) 77,515 European ancestry individuals NA Affymetrix [~ 79000000] (imputed) 3 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST011699 Genome-wide genotyping array 2021-05-19 33082346 Xu K 2020-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33082346 Genome-wide association study of smoking trajectory and meta-analysis of smoking status in 842,000 individuals. Smoking status (current vs never) 40,456 European ancestry current smokers, 13,511 African American current smokers, 2,920 Hispanic current smokers, 59,056 European ancestry mostly never smokers, 17,751 African American mostly never smokers, 7,195 Hispanic mostly never smokers NA Affymetrix [~ 79000000] (imputed) 22 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST011704 Genome-wide genotyping array 2020-02-07 31748690 Purves KL 2019-11-20 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31748690 A major role for common genetic variation in anxiety disorders. Lifetime anxiety disorder 25,453 European ancestry cases, 58,113 European ancestry controls 6,524 cases, 24001 controls Illumina [NR] (imputed) 5 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST009575 Genome-wide genotyping array 2020-02-07 31748690 Purves KL 2019-11-20 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31748690 A major role for common genetic variation in anxiety disorders. Anxiety symptoms 19,012 European ancestry cases, 58,113 European ancestry controls NA Illumina [NR] (imputed) 1 anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0007795 GCST009574 Genome-wide genotyping array 2020-04-17 31826910 Lu Y 2019-12-11 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31826910 Identification of novel loci and new risk variant in known loci for colorectal cancer risk in East Asians. Colorectal cancer 23,572 East Asian ancestry cases, 48,700 East Asian ancestry controls 58,131 European ancestry cases, 67,347 European ancestry controls Affymetrix, Illumina [up to 47000000] (imputed) 70 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST009869 Genome-wide genotyping array 2020-02-27 31830031 Chernus JM 2019-12-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31830031 A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. Maternal nondisjunction of chromosome 21 (mothers vs fathers) 705 mothers, 645 fathers NA Illumina [NR] (imputed) 14 Abnormality of chromosome segregation http://purl.obolibrary.org/obo/HP_0002916 GCST009704 Genome-wide genotyping array 2020-02-27 31830031 Chernus JM 2019-12-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31830031 A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. Maternal nondisjunction of chromosome 21 (MI error vs fathers) 535 mothers, 645 fathers NA Illumina [NR] (imputed) 10 Abnormality of chromosome segregation http://purl.obolibrary.org/obo/HP_0002916 GCST009707 Genome-wide genotyping array 2020-02-27 31830031 Chernus JM 2019-12-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31830031 A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. Maternal nondisjunction of chromosome 21 (MII error vs fathers) 157 mothers, 645 fathers NA Illumina [NR] (imputed) 13 Abnormality of chromosome segregation http://purl.obolibrary.org/obo/HP_0002916 GCST009706 Genome-wide genotyping array 2020-02-27 31830031 Chernus JM 2019-12-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31830031 A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21. Maternal nondisjunction of chromosome 21 (MI error vs MII error) 535 mothers (meiosis I error), 157 mothers (meiosis II error) NA Illumina [NR] (imputed) 10 Abnormality of chromosome segregation http://purl.obolibrary.org/obo/HP_0002916 GCST009705 Genome-wide genotyping array 2020-10-08 31928498 Lind L 2020-01-13 Metab Syndr Relat Disord www.ncbi.nlm.nih.gov/pubmed/31928498 Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank. Systolic blood pressure 291,107 British ancestry individuals NA Affymetrix [9463307] (imputed) 18 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST010662 Genome-wide genotyping array 2020-10-08 31928498 Lind L 2020-01-13 Metab Syndr Relat Disord www.ncbi.nlm.nih.gov/pubmed/31928498 Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank. Blood glucose levels 291,107 British ancestry individuals NA Affymetrix [9463307] (imputed) 17 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST010661 Genome-wide genotyping array 2020-10-08 31928498 Lind L 2020-01-13 Metab Syndr Relat Disord www.ncbi.nlm.nih.gov/pubmed/31928498 Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank. Triglyceride levels 291,107 British ancestry individuals NA Affymetrix [9463307] (imputed) 22 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST010660 Genome-wide genotyping array 2020-10-08 31928498 Lind L 2020-01-13 Metab Syndr Relat Disord www.ncbi.nlm.nih.gov/pubmed/31928498 Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank. Waist circumference 291,107 British ancestry individuals NA Affymetrix [9463307] (imputed) 23 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST010659 Genome-wide genotyping array 2020-10-08 31928498 Lind L 2020-01-13 Metab Syndr Relat Disord www.ncbi.nlm.nih.gov/pubmed/31928498 Genetic Determinants of Clustering of Cardiometabolic Risk Factors in U.K. Biobank. High density lipoprotein cholesterol levels 291,107 British ancestry individuals NA Affymetrix [9463307] (imputed) 22 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST010658 Genome-wide genotyping array 2020-03-23 31888606 Zhang S 2019-12-30 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/31888606 Region-based interaction detection in genome-wide case-control studies. Renal complication in type 2 diabetes 882 East Asian ancestry cases, 2,231 East Asian ancestry controls NA NR [1257031] 0 renal system measurement http://www.ebi.ac.uk/efo/EFO_0004742 GCST009778 Genome-wide genotyping array 2020-03-23 31888606 Zhang S 2019-12-30 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/31888606 Region-based interaction detection in genome-wide case-control studies. Myocardial infarction 2,967 cases, 3075 controls NA NR [649370] 4 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST009779 Genome-wide genotyping array 2020-04-17 31932636 Hebbar P 2020-01-13 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31932636 Genome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population. Fasting plasma glucose 1,353 Arab ancestry individuals 1,176 Arab ancestry individuals Illumina [632375] 9 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST009864 Genome-wide genotyping array 2021-02-17 31420016 Kisia LE 2019-08-16 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31420016 Genetic variation in interleukin-7 is associated with a reduced erythropoietic response in Kenyan children infected with Plasmodium falciparum. Severe malarial anemia in Plasmodium falciparum infection 70 child cases, 74 child controls 165 Kenyan ancestry child cases, 718 Kenyan ancestry child controls Illumina [NR] 0 severe malarial anemia http://www.ebi.ac.uk/efo/EFO_0010970 GCST011118 Genome-wide genotyping array 2019-12-10 31688885 Genetics of Glaucoma in People of African Descent (GGLAD) Consortium 2019-11-01 JAMA www.ncbi.nlm.nih.gov/pubmed/31688885 Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry. Glaucoma (primary open-angle) 694 African American cases, 1,590 Sub-Saharan African cases, 596 African American controls, 1,485 Sub-Saharan African controls 6,937 African ancestry cases, 14,917 African ancestry controls Illumina [6734161] (imputed) 1 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST009245 Genome-wide genotyping array 2020-02-06 31749835 Sangurdekar D 2019-11-04 Front Genet www.ncbi.nlm.nih.gov/pubmed/31749835 Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate. Severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis 42 European ancestry cases, 1,052 European ancestry controls NA Illumina [1016025] 3 response to dimethyl fumarate, lymphopenia http://www.ebi.ac.uk/efo/EFO_0010577, http://purl.obolibrary.org/obo/MONDO_0003783 GCST009546 Genome-wide genotyping array 2020-02-06 31749835 Sangurdekar D 2019-11-04 Front Genet www.ncbi.nlm.nih.gov/pubmed/31749835 Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate. Moderate or severe prolonged lymphopenia in dimethyl fumarate-treated relapsing-remitting multiple sclerosis 206 European ancestry cases, 1,052 European ancestry controls NA Illumina [1016018] 6 response to dimethyl fumarate, lymphopenia http://www.ebi.ac.uk/efo/EFO_0010577, http://purl.obolibrary.org/obo/MONDO_0003783 GCST009545 Genome-wide genotyping array 2020-02-11 31729369 Howles SA 2019-11-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31729369 Genetic variants of calcium and vitamin D metabolism in kidney stone disease. Kidney stones 6,536 British ancestry cases, 388,508 British ancestry controls NA Affymetrix [~ 8400000] (imputed) 15 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST009599 Genome-wide genotyping array 2020-02-11 31729369 Howles SA 2019-11-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31729369 Genetic variants of calcium and vitamin D metabolism in kidney stone disease. Kidney stones 6,536 British ancestry cases, 5,587 Japanese ancestry cases, 388,508 British ancestry controls, 28,870 Japanese ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 20 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST009598 Genome-wide genotyping array 2020-02-06 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. Interleukin-6 receptor subunit alpha levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST009561 Exome genotyping array [Exome array] 2020-02-06 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. C-X-C motif chemokine 10 levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST009562 Exome genotyping array [Exome array] 2020-02-06 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. CCL24 levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 CCL24 measurement http://www.ebi.ac.uk/efo/EFO_0009418 GCST009563 Exome genotyping array [Exome array] 2020-02-06 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. MHC class I polypeptide-related sequence A levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST009564 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. CD40 ligand levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST009565 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. CXCL5 levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 2 CXCL5 measurement http://www.ebi.ac.uk/efo/EFO_0009422 GCST009566 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. kallikrein-11 levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST009567 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. epithelial cell adhesion molecule levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 2 epithelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010574 GCST009568 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. interleukin 17 receptor B levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 interleukin 17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0008176 GCST009569 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. interleukin 12 receptor subunit beta-1 levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST009570 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. vascular endothelial growth factor D levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 2 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST009571 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. E-selectin levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST009572 Exome genotyping array [Exome array] 2020-02-07 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. melanoma-derived growth regulatory protein levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 2 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST009573 Exome genotyping array [Exome array] 2020-02-06 25147954 Enroth S 2014-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25147954 Strong effects of genetic and lifestyle factors on biomarker variation and use of personalized cutoffs. CCL19 levels up to 653 individuals up to 317 individuals Illumina [4840842] (imputed) 1 CCL19 measurement http://www.ebi.ac.uk/efo/EFO_0009415 GCST009558 Exome genotyping array [Exome array] 2021-01-27 32324875 Campbell PT 2020-04-23 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/32324875 Association of body mass index with colorectal cancer risk by genome-wide variants. Colorectal cancer x BMI interaction (2df) 14,059 European ancestry cases, 14,416 European ancestry controls NA Affymetrix, Illumina [2700000] (imputed) 1 colorectal adenocarcinoma, body mass index http://www.ebi.ac.uk/efo/EFO_0000365, http://www.ebi.ac.uk/efo/EFO_0004340 GCST010992 Genome-wide genotyping array 2020-05-14 32157176 Buchwald J 2020-03-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32157176 Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Nicotine metabolite ratio in current smokers 5,185 European ancestry individuals NA Illumina [9622178] (imputed) 2 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST009971 Genome-wide genotyping array 2020-05-14 32157176 Buchwald J 2020-03-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32157176 Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Cotinine and 3'-hydroxycotinine levels in current smokers 5,185 European ancestry individuals NA Illumina [9622178] (imputed) 3 cotinine measurement, trans-3-hydroxycotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813, http://www.ebi.ac.uk/efo/EFO_0010707 GCST009970 Genome-wide genotyping array 2020-05-14 32157176 Buchwald J 2020-03-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32157176 Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Cotinine levels in current smokers 5,185 European ancestry individuals, 3,700 individuals NA Illumina [9795096] (imputed) 0 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST009969 Genome-wide genotyping array 2020-05-14 32157176 Buchwald J 2020-03-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32157176 Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Smoking behaviour (cigarettes smoked per day) 4,772 European ancestry individuals NA Illumina [9622178] (imputed) 2 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST009968 Genome-wide genotyping array 2020-05-14 32157176 Buchwald J 2020-03-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32157176 Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Smoking behaviour (cigarette pack-years) 4,676 European ancestry individuals NA Illumina [9622178] (imputed) 2 pack-years measurement http://www.ebi.ac.uk/efo/EFO_0006526 GCST009967 Genome-wide genotyping array 2020-05-14 32157176 Buchwald J 2020-03-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32157176 Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Smoking intensity (cotinine levels/cigarettes per day) 4,772 European ancestry individuals NA Illumina [9622178] (imputed) 2 cotinine measurement, cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0007813, http://www.ebi.ac.uk/efo/EFO_0006525 GCST009966 Genome-wide genotyping array 2020-05-14 32157176 Buchwald J 2020-03-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32157176 Genome-wide association meta-analysis of nicotine metabolism and cigarette consumption measures in smokers of European descent. Cotinine levels in current smokers 5,185 European ancestry individuals NA Illumina [9622178] (imputed) 3 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST009965 Genome-wide genotyping array 2020-06-24 32332799 Song W 2020-04-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32332799 Genome-wide association analysis of insomnia using data from Partners Biobank. Insomnia 404,588 European ancestry individuals, 17,651 European, Hispanic and African ancestry individuals NA Illumina [5508534] (imputed) 17 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST010097 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Neuritic plaque 909 European ancestry individuals 369 individuals Affymetrix, Illumina [NR] (imputed) 14 neuritic plaque measurement http://www.ebi.ac.uk/efo/EFO_0006798 GCST90012825 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Neurofibrillary tangles 909 European ancestry individuals 369 individuals Affymetrix, Illumina [NR] (imputed) 16 neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006797 GCST90012826 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Diffuse plaques 909 European ancestry individuals 369 individuals Affymetrix, Illumina [NR] (imputed) 11 diffuse plaque measurement http://www.ebi.ac.uk/efo/EFO_0010699 GCST90012827 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Cerebral amyloid angiopathy 404 European ancestry mild cases, 209 European ancestry moderate cases, 113 European ancestry severe cases, 183 European ancestry controls 369 individuals Affymetrix, Illumina [NR] (imputed) 13 cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0006790 GCST90012828 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Microscopic brain infarct 253 European ancestry cases, 656 European ancestry controls 369 individuals Affymetrix, Illumina [NR] (imputed) 9 brain infarction http://www.ebi.ac.uk/efo/EFO_0004277 GCST90012829 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Macroscopic brain infarct 327 European ancestry cases, 582 European ancestry controls 369 individuals Affymetrix, Illumina [NR] (imputed) 5 brain infarction http://www.ebi.ac.uk/efo/EFO_0004277 GCST90012830 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Dementia with Lewy bodies 195 European ancestry cases, 714 European ancestry controls 369 individuals Affymetrix, Illumina [NR] (imputed) 13 Lewy body dementia http://www.ebi.ac.uk/efo/EFO_0006792 GCST90012831 Genome-wide genotyping array 2020-12-24 28322283 Chibnik LB 2017-03-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28322283 Susceptibility to neurofibrillary tangles: role of the PTPRD locus and limited pleiotropy with other neuropathologies. Neuropathologic traits (pleiotropy) 909 European ancestry individuals 369 individuals Affymetrix, Illumina [NR] (imputed) 22 brain infarction, neuritic plaque measurement, Lewy body dementia, cerebral amyloid angiopathy, neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0004277, http://www.ebi.ac.uk/efo/EFO_0006798, http://www.ebi.ac.uk/efo/EFO_0006792, http://www.ebi.ac.uk/efo/EFO_0006790, http://www.ebi.ac.uk/efo/EFO_0006797 GCST90012832 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Activity variability during wake 90,515 individuals NA NR [11024754] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST012040 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep duration (< 5 hours) 90,515 individuals NA NR [11024754] (imputed) 1 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST012039 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep duration (> 10 hours) 90,515 individuals NA NR [11024754] (imputed) 5 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST012038 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep start time 90,515 individuals NA NR [11024754] (imputed) 5 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST012037 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep end time 90,515 individuals NA NR [11024754] (imputed) 4 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST012036 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep (1-day periodicity) 90,515 individuals NA NR [11024754] (imputed) 5 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST012035 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep (1/2-day periodicity) 90,515 individuals NA NR [11024754] (imputed) 12 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST012034 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep (1/3-day periodicity) 90,515 individuals NA NR [11024754] (imputed) 19 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST012033 Genome-wide genotyping array 2021-07-19 33075057 Li X 2020-10-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33075057 Automated feature extraction from population wearable device data identified novel loci associated with sleep and circadian rhythms. Sleep activity levels 90,515 individuals NA NR [11024754] (imputed) 4 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST012041 Genome-wide genotyping array 2020-02-12 31735061 Liu X 2019-11-16 Aust N Z J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31735061 Wnt receptor gene FZD1 was associated with schizophrenia in genome-wide SNP analysis of the Australian Schizophrenia Research Bank cohort. Schizophrenia 429 European ancestry cases, 255 European ancestry controls NR Illumina [6473404] (imputed) 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST009603 Genome-wide genotyping array 2021-08-02 33106475 Li QS 2020-10-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33106475 Genome-wide association studies of antidepressant class response and treatment-resistant depression. Response to serotonin-norepinephrine reuptake inhibitors (responders vs non-responders) 4,030 European ancestry responders, 3,049 European ancestry non-responders NA Illumina [at least 560000] (imputed) 26 response to serotonin-norephinephrine reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0006325 GCST012159 Genome-wide genotyping array 2021-08-02 33106475 Li QS 2020-10-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33106475 Genome-wide association studies of antidepressant class response and treatment-resistant depression. Response to norepinephrine-dopamine reuptake inhibitors (responders vs non-responders) 3,971 European ancestry responders, 3,512 European ancestry non-responders NA Illumina [at least 560000] (imputed) 19 response to norepinephrine-dopamine reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0007870 GCST012158 Genome-wide genotyping array 2021-08-02 33106475 Li QS 2020-10-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33106475 Genome-wide association studies of antidepressant class response and treatment-resistant depression. Response to antidepressants (non-treatment-resistant vs treatment-resistant depression) 21,649 European ancestry individuals with non-treatment-resistant depression, 3,857 European ancestry individuals with treatment-resistant depression NA Illumina [at least 560000] (imputed) 27 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST012157 Genome-wide genotyping array 2021-08-02 33106475 Li QS 2020-10-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33106475 Genome-wide association studies of antidepressant class response and treatment-resistant depression. Response to SSRI (responders vs non-responders) 13,130 European ancestry responders, 6,610 European ancestry non-responders NA Illumina [at least 560000] (imputed) 15 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST012160 Genome-wide genotyping array 2020-01-30 31752434 Costa-Urrutia P 2019-11-19 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/31752434 Genome-Wide Association Study of Body Mass Index and Body Fat in Mexican-Mestizo Children. Childhood body mass index 828 Mexican-Mestizo ancestry individuals NA Affymetrix [~ 2500000] (imputed) 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009530 Genome-wide genotyping array 2020-01-30 31752434 Costa-Urrutia P 2019-11-19 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/31752434 Genome-Wide Association Study of Body Mass Index and Body Fat in Mexican-Mestizo Children. Body fat percentage 828 Mexican-Mestizo ancestry children NA Affymetrix [~ 2500000] (imputed) 11 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST009531 Genome-wide genotyping array 2019-12-17 31740666 Cheng Z 2019-11-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31740666 A regulatory variant of CHRM3 is associated with cannabis-induced hallucinations in European Americans. Hallucinations in long-term cannabis use 91 European ancestry cases, 220 African American cases, 1,826 European ancestry controls, 2,148 African American controls 256 European ancestry cases, 142 African American cases, 2,118 European ancestry controls, 1,114 African American controls Illumina [up to 14134502] (imputed) 2 Hallucinations http://purl.obolibrary.org/obo/HP_0000738 GCST009314 Genome-wide genotyping array 2020-02-13 31738745 Gibson J 2019-11-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31738745 A meta-analysis of genome-wide association studies of epigenetic age acceleration. Intrinsic epigenetic age acceleration 13,493 European ancestry individuals NA Illumina [5932107] (imputed) 10 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST009604 Genome-wide genotyping array 2020-02-13 31738745 Gibson J 2019-11-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31738745 A meta-analysis of genome-wide association studies of epigenetic age acceleration. Extrinsic epigenetic age acceleration 13,493 European ancestry individuals NA Illumina [5931171] (imputed) 1 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST009605 Genome-wide genotyping array 2021-07-08 33421400 Galata G 2021-01-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33421400 Genome-wide association study identifies novel susceptibility loci for KIT D816V positive mastocytosis. Mastocytosis (KIT D816V positive) 414 European ancestry cases, 9,504 European ancestry controls 621 European ancestry cases, 8,456 European ancestry controls Illumina [592007] (imputed) 7 Mastocytosis http://www.ebi.ac.uk/efo/EFO_0009001 GCST012017 Genome-wide genotyping array 2020-02-17 31813042 Wang L 2019-12-07 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/31813042 Additional common loci associated with stroke and obesity identified using pleiotropic analytical approach. Stroke and BMI (pleiotropy) 40,585 European ancestry stroke cases, 406,111 European ancestry controls, 681,275 European ancestry individuals NA NR [114466] (imputed) 0 stroke, body mass index http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0004340 GCST009639 Genome-wide genotyping array 2020-03-23 31900758 Han X 2020-01-03 Eur J Epidemiol www.ncbi.nlm.nih.gov/pubmed/31900758 Using Mendelian randomization to evaluate the causal relationship between serum C-reactive protein levels and age-related macular degeneration. C-reactive protein levels 418,642 British ancestry individuals NA NR [NR] 526 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST009777 Genome-wide genotyping array 2020-03-23 31900758 Han X 2020-01-03 Eur J Epidemiol www.ncbi.nlm.nih.gov/pubmed/31900758 Using Mendelian randomization to evaluate the causal relationship between serum C-reactive protein levels and age-related macular degeneration. Advanced age-related macular degeneration 12,711 European ancestry cases, 14,590 European ancestry controls NA NR [NR] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST009776 Genome-wide genotyping array 2019-05-08 29679657 Ferreira MA 2018-04-18 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/29679657 Eleven loci with new reproducible genetic associations with allergic disease risk. Allergic disease (asthma, hay fever or eczema) 180,129 European ancestry cases, 180,709 European ancestry controls NA NR [NR] 25 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST007732 Genome-wide genotyping array 2020-02-13 31748543 Johnston KJA 2019-11-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31748543 Identification of novel common variants associated with chronic pain using conditional false discovery rate analysis with major depressive disorder and assessment of pleiotropic effects of LRFN5. Chronic pain or major depressive disorder (pleiotropy) 10,543 European ancestry chronic pain cases, 43,028 major depressive disorder cases, 12,758 European ancestry controls, 87,522 controls NA NR [774292] 0 unipolar depression, Chronic pain http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/HP_0012532 GCST009607 Genome-wide genotyping array 2020-06-16 31791832 Koks S 2019-11-12 J Arthroplasty www.ncbi.nlm.nih.gov/pubmed/31791832 The Genetic Variations Associated With Time to Aseptic Loosening After Total Joint Arthroplasty. Time to aseptic loosening in total joint arthroplasty 97 individuals NA Illumina [up to 600000] 4 aseptic loosening http://www.ebi.ac.uk/efo/EFO_0010725 GCST010082 Genome-wide genotyping array 2020-06-16 31791832 Koks S 2019-11-12 J Arthroplasty www.ncbi.nlm.nih.gov/pubmed/31791832 The Genetic Variations Associated With Time to Aseptic Loosening After Total Joint Arthroplasty. Aseptic loosening in total joint arthroplasty 97 cases, 289 controls NA Illumina [up to 600000] 6 aseptic loosening http://www.ebi.ac.uk/efo/EFO_0010725 GCST010081 Genome-wide genotyping array 2020-11-05 32868391 Leng RX 2020-08-31 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32868391 Identification of new susceptibility loci associated with rheumatoid arthritis. Rheumatoid arthritis 5,900 East Asian cases, 20,521 East Asian controls, 14,361 European ancestry cases, 43,923 European ancestry controls NA Illumina [NR] (imputed) 5 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST010730 Genome-wide genotyping array 2021-04-16 32881892 Lin SH 2020-09-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/32881892 Low-frequency variation near common germline susceptibility loci are associated with risk of Ewing sarcoma. Ewing sarcoma 733 European ancestry cases, 1,346 European ancestry controls NA Illumina [16367531] (imputed) 3 Ewing sarcoma http://www.ebi.ac.uk/efo/EFO_0000174 GCST011498 Genome-wide genotyping array 2018-09-19 29973135 Rimpela JM 2018-07-04 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/29973135 Genome-wide association study of nocturnal blood pressure dipping in hypertensive patients. Systolic blood pressure night-to-day ratio in hypertension 204 Finnish ancestry individuals NA Illumina [631844] 2 systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006944 GCST006274 Genome-wide genotyping array 2018-09-19 29973135 Rimpela JM 2018-07-04 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/29973135 Genome-wide association study of nocturnal blood pressure dipping in hypertensive patients. Diastolic blood pressure night-to-day ratio in hypertension 204 Finnish ancestry individuals NA Illumina [631844] 5 diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006945 GCST006273 Genome-wide genotyping array 2021-07-09 32865774 Sima C 2020-08-31 Int Urol Nephrol www.ncbi.nlm.nih.gov/pubmed/32865774 Genome-wide association study of nephrolithiasis in an Eastern European population. Nephrolithiasis 329 Romanian ancestry cases, 5,105 Romanian ancestry controls NA Illumina [104390] 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST012019 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Dysmenorrheic pain severity 5,734 Japanese ancestry female individuals 5,614 Japanese ancestry female individuals Affymetrix [536506] 5 dysmenorrheic pain measurement http://www.ebi.ac.uk/efo/EFO_0007889 GCST006656 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (dysmenorrhea) 3,573 Japanese ancestry female cases, 2,161 Japanese ancestry female controls 3,580 Japanese ancestry female cases, 2,034 Japanese ancestry female controls Affymetrix [536506] 8 quality of life during menstruation measurement, dysmenorrheic pain measurement http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0007889 GCST006636 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Pain medicine use during menstruation 1,813 Japanese ancestry female cases, 3,921 Japanese ancestry female controls 1,494 Japanese ancestry female cases, 4,120 Japanese ancestry female controls Affymetrix [536506] 7 drug use measurement, quality of life during menstruation measurement http://www.ebi.ac.uk/efo/EFO_0007010, http://www.ebi.ac.uk/efo/EFO_0009366 GCST006637 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (fever) 112 Japanese ancestry female cases, 5,622 Japanese ancestry female controls 157 Japanese ancestry female cases, 5,457 Japanese ancestry female controls Affymetrix [536506] 2 quality of life during menstruation measurement, Fever http://www.ebi.ac.uk/efo/EFO_0009366, http://purl.obolibrary.org/obo/HP_0001945 GCST006638 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Heavy vaginal discharge 457 Japanese ancestry female cases, 5,277 Japanese ancestry female controls 471 Japanese ancestry female cases, 5,143 Japanese ancestry female controls Affymetrix [536506] 3 quality of life during menstruation measurement, vaginal discharge http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0009365 GCST006639 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (acne) 1,115 Japanese ancestry female cases, 4,619 Japanese ancestry female controls 1,204 Japanese ancestry female cases, 4,410 Japanese ancestry female controls Affymetrix [536506] 8 quality of life during menstruation measurement, acne http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0003894 GCST006640 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (aggressiveness) 899 Japanese ancestry female cases, 4,835 Japanese ancestry female controls 1,030 Japanese ancestry female cases, 4,584 Japanese ancestry female controls Affymetrix [536506] 5 quality of life during menstruation measurement, aggressive behavior http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0003015 GCST006641 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (increased appetite) 760 Japanese ancestry female cases, 4,974 Japanese ancestry female controls 903 Japanese ancestry female cases, 4,711 Japanese ancestry female controls Affymetrix [536506] 3 quality of life during menstruation measurement, eating behaviour http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0007829 GCST006642 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (bowel movement) 903 Japanese ancestry female cases, 4,831 Japanese ancestry female controls 921 Japanese ancestry female cases, 4,693 Japanese ancestry female controls Affymetrix [536506] 5 quality of life during menstruation measurement, Abnormal peristalsis http://www.ebi.ac.uk/efo/EFO_0009366, http://purl.obolibrary.org/obo/HP_0030914 GCST006643 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (depression) 1,863 Japanese ancestry female cases, 3,871 Japanese ancestry female controls 2,005 Japanese ancestry female cases, 3,609 Japanese ancestry female controls Affymetrix [536506] 1 quality of life during menstruation measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0003761 GCST006644 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (edema) 1,109 Japanese ancestry female cases, 4,625 Japanese ancestry female controls 1,331 Japanese ancestry female cases, 4,283 Japanese ancestry female controls Affymetrix [536506] 3 quality of life during menstruation measurement, edema http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0009373 GCST006645 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (headache) 1,758 Japanese ancestry female cases, 3,976 Japanese ancestry female controls 1,763 Japanese ancestry female cases, 3,851 Japanese ancestry female controls Affymetrix [536506] 4 quality of life during menstruation measurement, Headache http://www.ebi.ac.uk/efo/EFO_0009366, http://purl.obolibrary.org/obo/HP_0002315 GCST006646 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (joint pain) 251 Japanese ancestry female cases, 5,483 Japanese ancestry female controls 277 Japanese ancestry female cases, 5,337 Japanese ancestry female controls Affymetrix [536506] 4 quality of life during menstruation measurement, Arthralgia http://www.ebi.ac.uk/efo/EFO_0009366, http://purl.obolibrary.org/obo/HP_0002829 GCST006647 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (loss of concentration) 995 Japanese ancestry female cases, 4,739 Japanese ancestry female controls 1,081 Japanese ancestry female cases, 4,533 Japanese ancestry female controls Affymetrix [536506] 8 quality of life during menstruation measurement, decreased attention http://www.ebi.ac.uk/efo/EFO_0009366, http://purl.obolibrary.org/obo/NCIT_C117245 GCST006648 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (nervousness) 1,904 Japanese ancestry female cases, 3,830 Japanese ancestry female controls 2,017 Japanese ancestry female cases, 3,597 Japanese ancestry female controls Affymetrix [536506] 2 nervousness, quality of life during menstruation measurement http://purl.obolibrary.org/obo/NCIT_C74532, http://www.ebi.ac.uk/efo/EFO_0009366 GCST006649 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (pressure in breast) 642 Japanese ancestry female cases, 5,092 Japanese ancestry female controls 667 Japanese ancestry female cases, 4,947 Japanese ancestry female controls Affymetrix [536506] 4 quality of life during menstruation measurement, breast pressure measurement http://www.ebi.ac.uk/efo/EFO_0009366, http://www.ebi.ac.uk/efo/EFO_0009393 GCST006650 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (sleepiness) 1,902 Japanese ancestry female cases, 3,832 Japanese ancestry female controls 1,934 Japanese ancestry female cases, 3,680 Japanese ancestry female controls Affymetrix [536506] 3 quality of life during menstruation measurement, sleepiness http://www.ebi.ac.uk/efo/EFO_0009366, http://purl.obolibrary.org/obo/NCIT_C95746 GCST006651 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Menstruation quality of life impact (stiff neck) 937 Japanese ancestry female cases, 4,797 Japanese ancestry female controls 944 Japanese ancestry female cases, 4,670 Japanese ancestry female controls Affymetrix [536506] 4 quality of life during menstruation measurement, Stiff neck http://www.ebi.ac.uk/efo/EFO_0009366, http://purl.obolibrary.org/obo/HP_0025258 GCST006652 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Vaginal discharge (itching) 676 Japanese ancestry female cases, 5,058 Japanese ancestry female controls 669 Japanese ancestry female cases, 4,945 Japanese ancestry female controls Affymetrix [536506] 5 abnormal vaginal discharge itching http://www.ebi.ac.uk/efo/EFO_0009409 GCST006653 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Vaginal discharge (metrorrhagia) 406 Japanese ancestry female cases, 5,328 Japanese ancestry female controls 302 Japanese ancestry female cases, 5,312 Japanese ancestry female controls Affymetrix [536506] 2 vaginal discharge, Metrorrhagia http://www.ebi.ac.uk/efo/EFO_0009365, http://purl.obolibrary.org/obo/HP_0100608 GCST006657 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Vaginal discharge (smell) 367 Japanese ancestry female cases, 5,367 Japanese ancestry female controls 392 Japanese ancestry female cases, 5,222 Japanese ancestry female controls Affymetrix [536506] 5 abnormal vaginal discharge smell http://www.ebi.ac.uk/efo/EFO_0009408 GCST006654 Genome-wide genotyping array 2018-11-30 29855537 Hirata T 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855537 Japanese GWAS identifies variants for bust-size, dysmenorrhea, and menstrual fever that are eQTLs for relevant protein-coding or long non-coding RNAs. Breast size 5,609 Japanese ancestry female individuals NA Affymetrix [536506] 11 breast size http://www.ebi.ac.uk/efo/EFO_0004884 GCST006655 Genome-wide genotyping array 2018-09-19 29959729 Zhong XL 2018-06-29 Neurotox Res www.ncbi.nlm.nih.gov/pubmed/29959729 A Genome-Wide Association Study of α-Synuclein Levels in Cerebrospinal Fluid. Cerebrospinal fluid α-synuclein levels 59 European ancestry individuals with normal cognition, 101 European ancestry individuals with mild cognitive impairment, 49 European ancestry Alzheimer's disease cases NA Illumina [519442] 6 cerebrospinal fluid biomarker measurement, alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0006794, http://www.ebi.ac.uk/efo/EFO_0009323 GCST006279 Genome-wide genotyping array 2018-09-13 30004843 Ge S 2018-07-01 OMICS www.ncbi.nlm.nih.gov/pubmed/30004843 Type 2 Diabetes Mellitus: Integrative Analysis of Multiomics Data for Biomarker Discovery. Elevated fasting plasma glucose 76 Chinese ancestry cases, 435 Chinese ancestry controls NA Illumina [69485] 5 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST006257 Genome-wide genotyping array 2020-02-18 31666285 Olafsson S 2019-10-30 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31666285 Common and rare sequence variants influencing tumor biomarkers in blood. Serum alpha-fetoprotein levels 22,686 Icelandic ancestry individuals NA Illumina [NR] (imputed) 3 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST009651 Genome-wide genotyping array 2020-02-18 31666285 Olafsson S 2019-10-30 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31666285 Common and rare sequence variants influencing tumor biomarkers in blood. Serum carcinoembryonic antigen levels 22,309 Icelandic ancestry individuals NA Illumina [NR] (imputed) 11 serum carcinoembryonic antigen measurement http://www.ebi.ac.uk/efo/EFO_0005760 GCST009650 Genome-wide genotyping array 2020-02-18 31666285 Olafsson S 2019-10-30 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31666285 Common and rare sequence variants influencing tumor biomarkers in blood. Serum cancer antigen 15.3 levels 7,107 Icelandic ancestry individuals NA Illumina [NR] (imputed) 6 cancer antigen 15.3 measurement http://www.ebi.ac.uk/efo/EFO_0010585 GCST009649 Genome-wide genotyping array 2020-02-18 31666285 Olafsson S 2019-10-30 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31666285 Common and rare sequence variants influencing tumor biomarkers in blood. Serum cancer antigen 19.9 levels 9,945 Icelandic ancestry individuals NA Illumina [NR] (imputed) 4 cancer antigen 19.9 measurement http://www.ebi.ac.uk/efo/EFO_0010584 GCST009648 Genome-wide genotyping array 2020-02-18 31666285 Olafsson S 2019-10-30 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31666285 Common and rare sequence variants influencing tumor biomarkers in blood. Serum cancer antigen 125 (CA 125) levels 9,824 Icelandic ancestry individuals NA Illumina [NR] (imputed) 9 cancer antigen 125 measurement http://www.ebi.ac.uk/efo/EFO_0010603 GCST009647 Genome-wide genotyping array 2020-02-18 31666285 Olafsson S 2019-10-30 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31666285 Common and rare sequence variants influencing tumor biomarkers in blood. Serum alkaline phosphatase levels 162,774 Icelandic ancestry individuals NA Illumina [NR] (imputed) 50 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST009652 Genome-wide genotyping array 2020-01-09 31798171 Bonnemaijer PWM 2019-11-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31798171 Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. Optic cup area 24,493 European ancestry individuals NA Affymetrix, Illumina [11830838] (imputed) 24 optic cup area measurement http://www.ebi.ac.uk/efo/EFO_0006940 GCST009404 Genome-wide genotyping array 2020-01-09 31798171 Bonnemaijer PWM 2019-11-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31798171 Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. Optic disc area 24,509 European ancestry individuals NA Affymetrix, Illumina [11764957] (imputed) 18 optic disc area measurement http://www.ebi.ac.uk/efo/EFO_0006937 GCST009411 Genome-wide genotyping array 2020-01-09 31798171 Bonnemaijer PWM 2019-11-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31798171 Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. Vertical cup-disc ratio 25,180 European ancestry individuals NA Affymetrix, Illumina [11901698] (imputed) 24 cup-to-disc ratio measurement http://www.ebi.ac.uk/efo/EFO_0006939 GCST009412 Genome-wide genotyping array 2020-01-09 31798171 Bonnemaijer PWM 2019-11-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31798171 Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. Intraocular pressure 31,269 European ancestry individuals NA Affymetrix, Illumina [12426120] (imputed) 16 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST009413 Genome-wide genotyping array 2020-01-09 31798171 Bonnemaijer PWM 2019-11-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31798171 Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. Central corneal thickness 16,204 European ancestry individuals NA Affymetrix, Illumina [9249813] (imputed) 34 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST009414 Genome-wide genotyping array 2020-01-09 31798171 Bonnemaijer PWM 2019-11-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31798171 Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. Optic nerve head parameters (multi-trait analysis) up to 25,180 European ancestry individuals up to 7,792 Chinese ancestry individuals, 3,280 Malay ancestry individuals, 3,400 Indian ancestry individuals Affymetrix, Illumina [up to 11901698] (imputed) 7 cup-to-disc ratio measurement, optic cup area measurement, optic disc area measurement http://www.ebi.ac.uk/efo/EFO_0006939, http://www.ebi.ac.uk/efo/EFO_0006940, http://www.ebi.ac.uk/efo/EFO_0006937 GCST009416 Genome-wide genotyping array 2020-01-09 31798171 Bonnemaijer PWM 2019-11-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31798171 Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. Intraocular pressure and central corneal thickness (multi-trait analysis) up to 31,269 European ancestry individuals up to 7,792 Chinese ancestry individuals, 3,280 Malay ancestry individuals, 3,400 Indian ancestry individuals Affymetrix, Illumina [up to 12426120] (imputed) 8 central corneal thickness, intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0005213, http://www.ebi.ac.uk/efo/EFO_0004695 GCST009415 Genome-wide genotyping array 2018-07-04 29558500 Lee J 2018-03-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/29558500 Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations. Creatinine levels 7,064 Korean ancestry individuals 6,509 Korean ancestry individuals Affymetrix [345072] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST005791 Genome-wide genotyping array 2018-07-04 29558500 Lee J 2018-03-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/29558500 Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations. Glomerular filtration rate 7,064 Korean ancestry individuals 6,509 Korean ancestry individuals Affymetrix [345072] 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST005792 Genome-wide genotyping array 2018-07-04 29558500 Lee J 2018-03-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/29558500 Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations. Uric acid levels 7,064 Korean ancestry individuals 3,703 Korean ancestry individuals Affymetrix [345072] 6 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST005793 Genome-wide genotyping array 2018-07-04 29558500 Lee J 2018-03-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/29558500 Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations. Blood urea nitrogen levels 7,064 Korean ancestry individuals 6,509 Korean ancestry individuals Affymetrix [345072] 1 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST005794 Genome-wide genotyping array 2020-04-20 31794020 Matana A 2019-12-03 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31794020 Genome-wide analysis identifies two susceptibility loci for positive thyroid peroxidase and thyroglobulin antibodies. Thyroid autoantibody positivity (anti-thyroglobulin (TgAb) and/or anti-thyroid peroxidase (TPOAb) levels) 619 Croatian ancestry cases, 1,994 Croatian ancestry controls NA Illumina [7411206] (imputed) 4 thyroid peroxidase antibody measurement, anti-thyroglobulin antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666, http://www.ebi.ac.uk/efo/EFO_0009896 GCST009888 Genome-wide genotyping array 2018-08-10 24847101 Rudkowska I 2014-05-19 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/24847101 Genome-wide association study of the plasma triglyceride response to an n-3 polyunsaturated fatty acid supplementation. Response to long-chain n-3 polyunsaturated fatty acid supplementation (change in triglyceride levels) 81 responder individuals, 60 non-responder individuals NA Illumina [2668805] 5 triglyceride change measurement, response to long-chain n-3 PUFA dietary supplementation http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0009308 GCST006055 Genome-wide genotyping array 2018-10-05 29988085 Merino J 2018-07-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29988085 Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium. Dietary macronutrient intake 91,114 European ancestry individuals 177,315 European ancestry individuals Affymetrix, Illumina [1180000] (imputed) 5 energy intake http://www.ebi.ac.uk/efo/EFO_0003939 GCST006388 Genome-wide genotyping array 2018-09-05 29310926 Sharma A 2018-01-05 J Autoimmun www.ncbi.nlm.nih.gov/pubmed/29310926 Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort. Type 1 diabetes in high risk HLA genotype individuals (time to event) 5,806 European ancestry children NA Illumina [131847] 5 disease free survival, type 1 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000409, http://purl.obolibrary.org/obo/MONDO_0005147 GCST006196 Targeted genotyping array [ImmunoChip] 2018-09-05 29310926 Sharma A 2018-01-05 J Autoimmun www.ncbi.nlm.nih.gov/pubmed/29310926 Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort. Type 1 diabetes autoantibodies in high risk HLA genotype individuals (time to event) 5,806 European ancestry children NA Illumina [131847] 9 event free survival time, type 1 diabetes mellitus, autoantibody measurement http://www.ebi.ac.uk/efo/EFO_0000482, http://purl.obolibrary.org/obo/MONDO_0005147, http://www.ebi.ac.uk/efo/EFO_0004866 GCST006197 Targeted genotyping array [ImmunoChip] 2018-08-22 29953918 Deng C 2018-06-25 Gene www.ncbi.nlm.nih.gov/pubmed/29953918 Identification of three novel loci of ALDH2 Gene for Serum Folate levels in a Male Chinese Population by Genome-Wide Association Study. Serum folate levels 1,999 Han Chinese ancestry individuals NA Illumina [1940243] (imputed) 17 folic acid measurement http://www.ebi.ac.uk/efo/EFO_0005111 GCST006137 Genome-wide genotyping array 2020-04-17 32002517 Julienne H 2020-01-24 NAR Genom Bioinform www.ncbi.nlm.nih.gov/pubmed/32002517 JASS: command line and web interface for the joint analysis of GWAS results. Insulin-related traits (multivariate analysis) 62,205 individuals NA NR [3144808] (imputed) 27 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST009863 Genome-wide genotyping array 2020-10-15 32005708 Forgetta V 2020-01-31 Diabetes www.ncbi.nlm.nih.gov/pubmed/32005708 Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes. Type 1 diabetes 9,266 European ancestry cases, 15,574 European ancestry controls 4,329 European ancestry cases, 9,543 European ancestry controls Affymetrix, Illumina [9061522] (imputed) 6 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST010681 Genome-wide genotyping array 2021-03-22 32106291 Grunin M 2020-02-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/32106291 Association of a Variant in VWA3A with Response to Anti-Vascular Endothelial Growth Factor Treatment in Neovascular AMD. Response to anti-VEGF treatment in neovascular age-related macular degeneration (visual acuity) 187 Israeli ancestry individuals 108 Israeli ancestry individuals NR [5353842] (imputed) 0 age-related macular degeneration, response to anti-vascular endothelial growth factor drug http://www.ebi.ac.uk/efo/EFO_0001365, http://www.ebi.ac.uk/efo/EFO_0009467 GCST011376 Genome-wide genotyping array 2020-04-17 30402224 Yamada Y 2018-09-17 Biomed Rep www.ncbi.nlm.nih.gov/pubmed/30402224 Identification of 26 novel loci that confer susceptibility to early-onset coronary artery disease in a Japanese population. Coronary artery disease 1,482 Japanese ancestry cases, 5,774 Japanese ancestry controls NA Illumina [up to 244000] 10 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST009879 Exome genotyping array [Exome array] 2020-05-28 32109663 Feitosa MF 2020-02-14 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/32109663 Gene discovery for high-density lipoprotein cholesterol level change over time in prospective family studies. HDL cholesterol levels 3,567 European ancestry men, 4,171 European ancestry women NA Affymetrix, Illumina [6523511] (imputed) 12 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST009996 Genome-wide genotyping array 2018-07-16 29739929 Visconti A 2018-05-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29739929 Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. Low tan response 46,768 European ancestry low tanning cases, 74,528 European ancestry moderate and high tanning controls 15,547 European ancestry low tanning cases, 39,835 European moderate and high tanning ancestry controls Affymetrix [8351141] (imputed) 79 suntan http://www.ebi.ac.uk/efo/EFO_0004279 GCST005897 Genome-wide genotyping array 2018-07-16 29739929 Visconti A 2018-05-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29739929 Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure. Non-melanoma skin cancer 5,912 European ancestry cases, 181,740 European ancestry controls Affymetrix [5734850] (imputed) 82 non-melanoma skin carcinoma http://www.ebi.ac.uk/efo/EFO_0009260 GCST005896 Genome-wide genotyping array 2018-06-05 29760442 Iglesias AI 2018-05-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29760442 Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Central corneal thickness 17,803 European ancestry individuals, 8,107 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 46 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST005667 Genome-wide genotyping array 2018-09-27 29760442 Iglesias AI 2018-05-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29760442 Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Central corneal thickness 17,803 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 14 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST006366 Genome-wide genotyping array 2018-09-27 29760442 Iglesias AI 2018-05-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29760442 Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Central corneal thickness 8,107 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST006367 Genome-wide genotyping array 2018-10-04 30003630 Minica CC 2018-07-13 Addiction www.ncbi.nlm.nih.gov/pubmed/30003630 GENOME-WIDE ASSOCIATION META-ANALYSIS OF AGE AT FIRST CANNABIS USE. Cannabis use (age at onset) 24,953 European ancestry individuals 3,735 European ancestry individuals Affymetrix, Illumina, Perlegen [6163759] (imputed) 3 Cannabis use, age at onset http://www.ebi.ac.uk/efo/EFO_0007585, http://www.ebi.ac.uk/efo/EFO_0004847 GCST006386 Genome-wide genotyping array 2021-04-16 32876488 Meeks KAC 2020-09-02 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32876488 The Genetics of Circulating Resistin Level, A Biomarker for Cardiovascular Diseases, Is Informed by Mendelian Randomization and the Unique Characteristics of African Genomes. Resistin levels 3,754 Sub-Saharan African ancestry individuals, 1,867 African American individuals NA Affymetrix [NR] (imputed) 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST011497 Genome-wide genotyping array 2020-01-15 31792241 Gouveia MH 2019-12-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31792241 Genetics of cognitive trajectory in Brazilians: 15 years of follow-up from the Bambuí-Epigen Cohort Study of Aging. Cognitive decline (age-related) 1,407 Brazilian ancestry individuals NA Illumina [at least 2500000] (imputed) 13 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST009433 Genome-wide genotyping array 2020-02-05 31372216 Haaland OA 2019-06-24 F1000Res www.ncbi.nlm.nih.gov/pubmed/31372216 A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption. Cleft lip with or without cleft palate x maternal periconceptional alcohol use interaction (parent of origin effect) 825 European ancestry case-parent duos or trios, 1,024 Asian ancestry case-parent duos or trios, 59 case-parent duos or trios NA NR [341191] 3 Cleft palate, cleft lip, alcohol exposure measurement, parental genotype effect measurement http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959, http://www.ebi.ac.uk/efo/EFO_0009113, http://www.ebi.ac.uk/efo/EFO_0005939 GCST009542 Genome-wide genotyping array 2020-02-05 31372216 Haaland OA 2019-06-24 F1000Res www.ncbi.nlm.nih.gov/pubmed/31372216 A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption. Cleft lip with or without cleft palate x maternal periconceptional smoking interaction (parent of origin effect) 825 European ancestry case-parent duos or trios, 1,024 Asian ancestry case-parent duos or trios, 59 case-parent duos or trios NA NR [341191] 9 Cleft palate, tobacco smoke exposure measurement, cleft lip, parental genotype effect measurement http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0009115, http://www.ebi.ac.uk/efo/EFO_0003959, http://www.ebi.ac.uk/efo/EFO_0005939 GCST009544 Genome-wide genotyping array 2020-02-05 31372216 Haaland OA 2019-06-24 F1000Res www.ncbi.nlm.nih.gov/pubmed/31372216 A genome-wide scan of cleft lip triads identifies parent-of-origin interaction effects between ANK3 and maternal smoking, and between ARHGEF10 and alcohol consumption. Cleft lip with or without cleft palate x maternal periconceptional vitamin use interaction (parent of origin effect) 825 European ancestry case-parent duos or trios, 1,024 Asian ancestry case-parent duos or trios, 59 case-parent duos or trios NA NR [341191] 8 vitamin supplement exposure measurement, Cleft palate, cleft lip, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0009116, http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959, http://www.ebi.ac.uk/efo/EFO_0005939 GCST009543 Genome-wide genotyping array 2018-12-19 30271922 Clifton EAD 2018-05-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30271922 Genome-wide association study for risk taking propensity indicates shared pathways with body mass index. Self-reported risk-taking behaviour 113,882 European ancestry cases, 322,354 European ancestry controls NA Affymetrix [7736308] (imputed) 26 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST006810 Genome-wide genotyping array 2018-12-19 30271922 Clifton EAD 2018-05-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30271922 Genome-wide association study for risk taking propensity indicates shared pathways with body mass index. Body mass index 772,825 individuals NA Affymetrix [NR] 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST006811 Genome-wide genotyping array 2018-12-19 30271922 Clifton EAD 2018-05-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30271922 Genome-wide association study for risk taking propensity indicates shared pathways with body mass index. Smoking status (ever vs never smokers) 207,229 European ancestry ever smoker cases, 243,177 European ancestry never smoker controls NA Affymetrix [7736308] (imputed) 7 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST006812 Genome-wide genotyping array 2018-08-23 29883787 Gregson CL 2018-06-05 Bone www.ncbi.nlm.nih.gov/pubmed/29883787 Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. Bone mineral density (total hip) 232 European ancestry high BMD individuals, 1,026 European ancestry moderate high BMD individuals, 852 European ancestry low BMD individuals NA Illumina [6379332] (imputed) 18 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST006143 Genome-wide genotyping array 2018-08-23 29883787 Gregson CL 2018-06-05 Bone www.ncbi.nlm.nih.gov/pubmed/29883787 Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. High bone mineral density 232 European ancestry cases, 5,667 population controls NA NR [NR] 0 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST006141 Genome-wide genotyping array 2018-08-23 29883787 Gregson CL 2018-06-05 Bone www.ncbi.nlm.nih.gov/pubmed/29883787 Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes. Lumbar spine bone mineral density 232 European ancestry high BMD individuals, 613 European ancestry moderate high BMD individuals, 535 European ancestry low BMD individuals 30,970 individuals Illumina [6379332] (imputed) 0 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST006142 Genome-wide genotyping array 2018-09-06 29769613 Sun X 2018-05-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29769613 Genetic variant for behavioral regulation factor of executive function and its possible brain mechanism in attention deficit hyperactivity disorder. Executive function in ADHD 547 East Asian ancestry cases NA Affymetrix [644166] 1 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST006219 Genome-wide genotyping array 2018-08-13 29891935 Choquet H 2018-06-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29891935 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Glaucoma (primary open-angle) 3,836 European ancestry cases, 48,065 European ancestry controls, 411 Hispanic cases, 4,778 Hispanic controls, 441 East Asian ancestry cases, 4,034 East Asian ancestry controls, 298 African American cases, 1,549 African American controls 6,687 European ancestry cases, 155,514 European ancestry controls, 204 South Asian ancestry cases, 4,916 South Asian ancestry controls, 272 African British cases, 4,831 African British controls, 22 East Asian ancestry cases, 873 East Asian ancestry controls, 144 mixed ancestry cases, 3,427 mixed ancestry controls Affymetrix [at least 665500] (imputed) 9 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST006066 Genome-wide genotyping array 2018-08-13 29891935 Choquet H 2018-06-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29891935 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Glaucoma (primary open-angle) 6,687 European ancestry cases, 155,514 European ancestry controls, 204 South Asian ancestry cases, 4,916 South Asian ancestry controls, 272 African British cases, 4,831 African British controls, 22 East Asian ancestry cases, 873 East Asian ancestry controls, 144 mixed ancestry cases, 3,427 mixed ancestry controls 3,836 European ancestry cases, 48,065 European ancestry controls, 411 Hispanic cases, 4,778 Hispanic controls, 441 East Asian ancestry cases, 4,034 East Asian ancestry controls, 298 African American cases, 1,549 African American controls NR [NR] (imputed) 9 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST006067 Genome-wide genotyping array 2018-08-13 29891935 Choquet H 2018-06-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29891935 A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci. Glaucoma (primary open-angle) 10,523 European ancestry cases, 203,579 European ancestry controls, 411 Hispanic cases, 4,778 Hispanic controls, 463 East Asian ancestry cases, 4,907 East Asian ancestry controls, 298 African American cases, 1,549 African American controls, 204 South Asian ancestry cases, 4,916 South Asian ancestry controls, 272 African British cases, 4,831 African British controls, 144 mixed ancestry cases, 3,427 mixed ancestry controls NA Affymetrix [at least 665500] (imputed) 47 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST006065 Genome-wide genotyping array 2018-10-16 30003307 Fall T 2018-07-12 Diabetologia www.ncbi.nlm.nih.gov/pubmed/30003307 Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank. Coronary artery disease in diabetes 3,968 British ancestry cases, 11,698 British ancestry controls NA Affymetrix [9087334] (imputed) 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST006405 Genome-wide genotyping array 2021-04-09 32869517 Sung H 2020-08-31 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/32869517 Genome-wide association study of café-au-lait macule number in neurofibromatosis type 1. Café-au-lait macule number in neurofibromatosis type1 112 European ancestry individuals 59 European ancestry individuals Illumina [608561] 2 Cafe-au-lait spot http://purl.obolibrary.org/obo/HP_0000957 GCST011464 Genome-wide genotyping array 2020-02-10 28855172 den Hollander W 2017-08-30 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/28855172 Genome-wide association and functional studies identify a role for matrix Gla protein in osteoarthritis of the hand. Osteoarthritis of the hand 8,743 individuals 2,836 European ancestry individuals, 1,175 individuals Illumina [~ 11000000] (imputed) 5 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST009596 Genome-wide genotyping array 2021-04-07 32888428 Krebs K 2020-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32888428 Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy. Penicillin allergy 29,396 European ancestry cases, 452,094 European ancestry controls 87,996 European ancestry cases, 1,031,087 European ancestry controls Affymetrix [19724685] (imputed) 1 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST011458 Genome-wide genotyping array 2019-05-15 30805717 Zhu Z 2019-02-25 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30805717 Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis. Alzheimer's disease or fasting glucose levels (pleiotropy) 54,162 European ancestry cases, 58,047 European ancestry individuals NA NR [NR] 4 Alzheimer disease, fasting blood glucose measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004465 GCST007825 Genome-wide genotyping array 2019-05-15 30805717 Zhu Z 2019-02-25 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30805717 Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis. Alzheimer's disease or fasting insulin levels (pleiotropy) 54,162 European ancestry cases, 51,750 European ancestry individuals NA NR [NR] 3 Alzheimer disease, fasting blood insulin measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004466 GCST007826 Genome-wide genotyping array 2019-05-15 30805717 Zhu Z 2019-02-25 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30805717 Shared genetic architecture between metabolic traits and Alzheimer's disease: a large-scale genome-wide cross-trait analysis. Alzheimer's disease or HDL levels (pleiotropy) 54,162 European ancestry cases, 60,812 European ancestry individuals NA NR [NR] 20 Alzheimer disease, high density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004612 GCST007827 Genome-wide genotyping array 2020-05-28 32019955 Brcic L 2020-02-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32019955 AATF and SMARCA2 are associated with thyroid volume in Hashimoto's thyroiditis patients. Thyroid volume in Hashimoto’s thyroiditis 345 European ancestry individuals NA Illumina [6007542] (imputed) 8 thyroid volume http://www.ebi.ac.uk/efo/EFO_0004865 GCST009997 Genome-wide genotyping array 2018-07-25 29769526 Estrada K 2018-05-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29769526 A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. Neuromyelitis optica 66 European ancestry AQP4-IgG antibody seropositive cases, 63 European ancestry AQP4-IgG antibody seronegative cases, 784 European ancestry controls 66 European ancestry AQP4-IgG antibody seropositive cases, 20 European ancestry AQP4-IgG antibody seronegative cases, 460 European ancestry controls Affymetrix [6804788] (imputed) 7 neuromyelitis optica http://www.ebi.ac.uk/efo/EFO_0004256 GCST005964 Genome-wide genotyping array 2019-01-22 29769526 Estrada K 2018-05-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29769526 A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. Neuromyelitis optica (AQP4-IgG-positive) 66 European ancestry cases, 784 European ancestry controls 66 European ancestry cases, 460 European ancestry controls Affymetrix [6804788] (imputed) 7 AQP4-IgG-positive neuromyelitis optica http://www.ebi.ac.uk/efo/EFO_0009584 GCST006937 Genome-wide genotyping array 2019-01-22 29769526 Estrada K 2018-05-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29769526 A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica. Neuromyelitis optica (AQP4-IgG-negative) 63 European ancestry cases, 784 European ancestry controls 20 European ancestry cases, 460 European ancestry controls Affymetrix [6804788] (imputed) 0 AQP4-IgG-negative neuromyelitis optica http://www.ebi.ac.uk/efo/EFO_0009585 GCST006938 Genome-wide genotyping array 2020-01-10 31792237 Yang BZ 2019-12-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31792237 Genomewide Gene-by-Sex Interaction Scans Identify ADGRV1 for Sex Differences in Opioid Dependent African Americans. Opioid dependence x sex interaction 2,603 African American cases, 2,341 African American controls, 2,112 European ancestry cases, 1,331 European ancestry controls NA Illumina [up to 8775706] (imputed) 9 sex interaction measurement, opioid dependence http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0005611 GCST009419 Genome-wide genotyping array 2018-07-12 29762745 Claus EB 2018-05-12 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/29762745 Genome-wide association analysis identifies a meningioma risk locus at 11p15.5. Meningioma 1,606 European ancestry cases, 9,823 European ancestry controls 114 European ancestry cases, 406 European ancestry controls, 418 cases, 1,852 controls Affymetrix, Illumina [up to 9213034] (imputed) 1 meningioma http://purl.obolibrary.org/obo/MONDO_0016642 GCST005870 Genome-wide genotyping array 2021-06-03 31797917 Ward J 2019-12-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31797917 Novel genome-wide associations for anhedonia, genetic correlation with psychiatric disorders, and polygenic association with brain structure. Anhedonia 375,724 European ancestry individuals 93,559 individuals Affymetrix [NR] 0 anhedonia measurement http://www.ebi.ac.uk/efo/EFO_0009587 GCST011778 Genome-wide genotyping array 2018-07-11 28658209 Huang H 2017-06-28 Nature www.ncbi.nlm.nih.gov/pubmed/28658209 Fine-mapping inflammatory bowel disease loci to single-variant resolution. Inflammatory bowel disease up to 20,155 European ancestry Crohn's disease cases, up to 15,191 European ancestry ulcerative colitis cases, up to 34,257 European ancestry controls NA Illumina [161681] (imputed) 0 ulcerative colitis, Crohn's disease, inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0000384, http://www.ebi.ac.uk/efo/EFO_0003767 GCST005837 Targeted genotyping array [ImmunoChip] 2018-09-14 29967481 Joo YB 2018-07-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29967481 Genetic variants in systemic lupus erythematosus susceptibility loci, XKR6 and GLT1D1 are associated with childhood-onset SLE in a Korean cohort. Childhood onset systemic lupus erythematosus 96 Korean ancestry childhood onset cases, 685 Korean ancestry adult onset cases NA Illumina [648077] 2 systemic lupus erythematosus, age at onset http://purl.obolibrary.org/obo/MONDO_0007915, http://www.ebi.ac.uk/efo/EFO_0004847 GCST006260 Genome-wide genotyping array 2018-09-20 29808027 Tedja MS 2018-05-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29808027 Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Spherical equivalent 41,073 European ancestry individuals, 2,610 Erasmus Rucphen (founder/genetic isolate) individuals, 509 Talana (founder/genetic isolate) individuals, 15,044 East Asian ancestry individuals, 2,275 Malay ancestry individuals, 2,110 Indian ancestry individuals, 2,506 Asian ancestry individuals NA Affymetrix, Illumina [~ 9300000] (imputed) 49 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST006289 Genome-wide genotyping array 2018-09-20 29808027 Tedja MS 2018-05-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29808027 Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Myopia (age of diagnosis) 104,293 European ancestry individuals NA Illumina [~ 10600000] (imputed) 112 age of onset of myopia http://purl.obolibrary.org/obo/OBA_2001030 GCST006290 Genome-wide genotyping array 2018-09-20 29808027 Tedja MS 2018-05-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29808027 Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Spherical equivalent or myopia (age of diagnosis) 145,366 European ancestry individuals, 2,610 Erasmus Rucphen (founder/genetic isolate) individuals, 509 Talana (founder/genetic isolate) individuals, 15,044 East Asian ancestry individuals, 2,275 Malay ancestry individuals, 2,110 Indian ancestry individuals, 2,506 Asian ancestry individuals NA Affymetrix, Illumina [~ 11000000] (imputed) 140 refractive error, age of onset of myopia http://purl.obolibrary.org/obo/MONDO_0004892, http://purl.obolibrary.org/obo/OBA_2001030 GCST006291 Genome-wide genotyping array 2018-08-24 28838971 Mercader JM 2017-08-24 Diabetes www.ncbi.nlm.nih.gov/pubmed/28838971 A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 Diabetes. Type 2 diabetes 4,052 Hispanic cases and 4,606 Hispanic controls 2,071 Hispanic cases, 5,749 Hispanic controls, 1,519 Pima Indian ancestry cases, 1,680 Pima Indian ancestry controls, 427 Indigenous Mexican ancestry cases, 751 Indigenous Mexican ancestry controls. Illumina [158892] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST006145 Exome genotyping array [Exome array] 2020-10-27 31811950 Penney KL 2019-12-04 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/31811950 Genetic Variant Associated with Survival of Patients with Stage II-III Colon Cancer. Disease free survival in colon cancer 4,319 European ancestry cases, 358 African American cases, 190 Asian cases, 107 cases NA Illumina [873829] (imputed) 1 disease free survival http://www.ebi.ac.uk/efo/EFO_0000409 GCST010717 Genome-wide genotyping array 2020-10-27 31811950 Penney KL 2019-12-04 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/31811950 Genetic Variant Associated with Survival of Patients with Stage II-III Colon Cancer. Survival in colon cancer 4,319 European ancestry cases, 358 African American cases, 190 Asian cases, 107 cases NA Illumina [873829] (imputed) 1 overall survival http://www.ebi.ac.uk/efo/EFO_0000638 GCST010716 Genome-wide genotyping array 2018-08-09 29847655 Fan BJ 2018-05-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/29847655 Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. Central corneal thickness 195 South Indian ancestry individuals from 15 families 1,520 Singaporean Indian individuals, 4,038 Mexican American individuals, 6,911 European ancestry individuals Illumina [1223314] 1 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST006050 Genome-wide genotyping array 2018-08-09 29847655 Fan BJ 2018-05-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/29847655 Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness Locus. Central corneal thickness 195 South Indian ancestry individuals from 15 families 4,038 Mexican American individuals, 4,806 European ancestry individuals Illumina [1223314] 2 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST006049 Genome-wide genotyping array 2018-10-17 29971594 Rosenberger A 2018-07-03 Int Arch Occup Environ Health www.ncbi.nlm.nih.gov/pubmed/29971594 Genetic modifiers of radon-induced lung cancer risk: a genome-wide interaction study in former uranium miners. Lung cancer x radon exposure interaction (1df) 49 European ancestry high radon exposure cases, 15,028 European ancestry low radon exposure cases, 259 European ancestry high radon exposure controls, 13,263 European ancestry low radon exposure controls NA Illumina [407117] 3 lung carcinoma, radon exposure measurement http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0009370 GCST006413 Genome-wide genotyping array 2020-01-21 31786426 Farias Tempaku P 2019-08-14 Sleep Med www.ncbi.nlm.nih.gov/pubmed/31786426 Genome-wide association study reveals two novel risk alleles for incident obstructive sleep apnea in the EPISONO cohort. Obstructive sleep apnea trait (apnea hypopnea index, change over time) 404 European ancestry individuals, 97 Black individuals, 20 Asian ancestry individuals, 20 Indigenous individuals, 138 mixed race individuals, 27 individuals NA Illumina [up to 730525] 25 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST009461 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Behavioural changes in frontotemporal lobe dementia 262 European ancestry cases, 120 European ancestry controls NA Illumina [7033776] (imputed) 3 behavior http://purl.obolibrary.org/obo/GO_0007610 GCST006146 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Frontotemporal dementia (age at onset) 382 European ancestry GRN mutation carrier individuals 67 European ancestry GRN mutation carrier individuals, 143 European ancestry GRN negative individuals Illumina [7033776] (imputed) 5 age of onset of frontotemporal dementia http://purl.obolibrary.org/obo/OBA_2001022 GCST006147 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Frontotemporal dementia with GRN mutation 382 European ancestry cases, 1,146 European ancestry controls 67 European ancestry cases, 1,798 European ancestry controls Illumina [7033776] (imputed) 12 frontotemporal dementia http://purl.obolibrary.org/obo/MONDO_0017276 GCST006148 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Frontotemporal dementia with GRN mutation (age at onset) 382 European ancestry individuals 67 European ancestry individuals Illumina [7033776] (imputed) 6 age of onset of frontotemporal dementia http://purl.obolibrary.org/obo/OBA_2001022 GCST006149 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Frontotemporal dementia 382 European ancestry GRN mutation carrier cases, 1,146 European ancestry controls 143 European ancestry GRN negative cases, 1,798 European ancestry controls Illumina [7033776] (imputed) 0 frontotemporal dementia http://purl.obolibrary.org/obo/MONDO_0017276 GCST006150 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Memory dysfunction in frontotemporal lobe dementia 139 European ancestry cases, 243 European ancestry controls NA Illumina [7033776] (imputed) 6 memory impairment http://www.ebi.ac.uk/efo/EFO_0001072 GCST006151 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Language impairment in frontotemporal lobe dementia 169 European ancestry cases, 213 European ancestry controls NA Illumina [7033776] (imputed) 2 language impairment http://www.ebi.ac.uk/efo/EFO_0005425 GCST006152 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Parkinsonism in frontotemporal lobe dementia 184 European ancestry cases, 198 European ancestry controls NA Illumina [7033776] (imputed) 3 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST006153 Genome-wide genotyping array 2018-08-24 29724592 Pottier C 2018-04-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/29724592 Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study. Frontotemporal dementia 382 European ancestry GRN mutation carrier cases, 1,146 European ancestry controls 67 GRN mutation carrier European ancestry cases, 143 GRN-negative European ancestry cases, 1,798 European ancestry controls Illumina [7033776] (imputed) 6 frontotemporal dementia http://purl.obolibrary.org/obo/MONDO_0017276 GCST006154 Genome-wide genotyping array 2021-04-28 32890573 Yan Q 2020-09-02 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32890573 A genome-wide association study of asthma hospitalizations in adults. Exacerbations requiring hospitalisation in asthma 1,658 British ancestry cases, 32,509 British ancestry controls NA Affymetrix [87696888] (imputed) 36 asthma exacerbation measurement http://www.ebi.ac.uk/efo/EFO_0007614 GCST011570 Genome-wide genotyping array 2018-09-25 29975729 Kim TH 2018-07-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/29975729 Identification of novel susceptibility loci associated with hepatitis B surface antigen seroclearance in chronic hepatitis B. Hepatitis B surface antigen seroclearance in chronic hepatitis B infection 100 Korean ancestry cases, 100 Korean ancestry controls NA Illumina [1365088] 4 Hepatitis B virus surface antigen seropositivity http://www.ebi.ac.uk/efo/EFO_0009345 GCST006364 Genome-wide genotyping array 2018-08-15 29895819 Endo C 2018-06-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29895819 Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Freckles 7,148 Japanese ancestry female cases, 4,034 Japanese ancestry female controls NA Affymetrix [536506] 7 freckles http://www.ebi.ac.uk/efo/EFO_0003963 GCST006091 Genome-wide genotyping array 2018-08-15 29895819 Endo C 2018-06-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29895819 Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Double-edged eyelids 2,069 Japanese ancestry female cases, 3,545 Japanese ancestry female controls NA Affymetrix [536506] 2 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST006092 Genome-wide genotyping array 2018-08-15 29895819 Endo C 2018-06-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29895819 Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Thick vs thin eyebrows 1,153 Japanese ancestry female thick eyebrow individuals, 2,788 Japanese ancestry female thin eyebrow individuals NA Affymetrix [536506] 1 facial hair thickness measurement http://www.ebi.ac.uk/efo/EFO_0007823 GCST006093 Genome-wide genotyping array 2018-08-15 29895819 Endo C 2018-06-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29895819 Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Straight vs curly hair 2,532 Japanese ancestry female straight hair individuals, 2,346 Japanese ancestry female curly hair individuals NA Affymetrix [536506] 1 hair morphology measurement http://www.ebi.ac.uk/efo/EFO_0007821 GCST006094 Genome-wide genotyping array 2018-08-15 29895819 Endo C 2018-06-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29895819 Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Excessive hairiness 3,830 Japanese ancestry female cases, 7,414 Japanese ancestry female controls NA Affymetrix [536506] 6 Hirsutism http://purl.obolibrary.org/obo/HP_0001007 GCST006095 Genome-wide genotyping array 2018-08-15 29895819 Endo C 2018-06-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29895819 Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Excessive sweating 1,245 Japanese ancestry female cases, 3,293 Japanese ancestry female controls NA Affymetrix [536506] 3 Hyperhidrosis http://purl.obolibrary.org/obo/HP_0000975 GCST006090 Genome-wide genotyping array 2018-08-15 29895819 Endo C 2018-06-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29895819 Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations. Age spots 3,815 Japanese ancestry female cases, 7,438 Japanese ancestry female controls NA Affymetrix [536506] 3 solar lentigines measurement http://www.ebi.ac.uk/efo/EFO_0007850 GCST006096 Genome-wide genotyping array 2018-06-05 29246731 de Toro-Martin J 2017-11-02 J Clin Lipidol www.ncbi.nlm.nih.gov/pubmed/29246731 A common variant in ARHGEF10 alters delta-6 desaturase activity and influence susceptibility to hypertriglyceridemia. Delta-5 desaturase activity response to n3-polyunsaturated fat supplement 81 extreme responder individuals, 60 non-responder individuals NA Illumina [2668805] 6 delta-5 desaturase measurement, response to polyunsaturated fatty acid supplementation http://www.ebi.ac.uk/efo/EFO_0007764, http://www.ebi.ac.uk/efo/EFO_0009131 GCST005668 Genome-wide genotyping array 2018-06-05 29246731 de Toro-Martin J 2017-11-02 J Clin Lipidol www.ncbi.nlm.nih.gov/pubmed/29246731 A common variant in ARHGEF10 alters delta-6 desaturase activity and influence susceptibility to hypertriglyceridemia. Delta-6 desaturase activity response to n3-polyunsaturated fat supplement 81 extreme responder individuals, 60 non-responder individuals NA Illumina [2668805] 1 delta-6 desaturase measurement, response to polyunsaturated fatty acid supplementation http://www.ebi.ac.uk/efo/EFO_0007765, http://www.ebi.ac.uk/efo/EFO_0009131 GCST005669 Genome-wide genotyping array 2020-02-19 31993563 Ware EB 2019-11-22 Mayo Clin Proc Innov Qual Outcomes www.ncbi.nlm.nih.gov/pubmed/31993563 Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid. Urinary calcium excretion 6,462 European ancestry individuals NA NR [NR] (imputed) 15 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST009676 Genome-wide genotyping array 2020-02-19 31993563 Ware EB 2019-11-22 Mayo Clin Proc Innov Qual Outcomes www.ncbi.nlm.nih.gov/pubmed/31993563 Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid. Urinary magnesium excretion 6,462 European ancestry individuals NA NR [NR] (imputed) 9 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST009675 Genome-wide genotyping array 2020-02-19 31993563 Ware EB 2019-11-22 Mayo Clin Proc Innov Qual Outcomes www.ncbi.nlm.nih.gov/pubmed/31993563 Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid. Urinary uric acid excretion 6,462 European ancestry individuals NA NR [NR] (imputed) 3 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST009674 Genome-wide genotyping array 2020-07-06 31993563 Ware EB 2019-11-22 Mayo Clin Proc Innov Qual Outcomes www.ncbi.nlm.nih.gov/pubmed/31993563 Genome-wide Association Study of 24-Hour Urinary Excretion of Calcium, Magnesium, and Uric Acid. Urinary volume 6,462 European ancestry individuals NA NR [NR] (imputed) 3 urine volume measurement http://www.ebi.ac.uk/efo/EFO_0010604 GCST010120 Genome-wide genotyping array 2019-04-09 30808845 Thio CHL 2019-02-26 Am J Nephrol www.ncbi.nlm.nih.gov/pubmed/30808845 Genome-Wide Association Scan of Serum Urea in European Populations Identifies Two Novel Loci. Serum urea levels 13,312 European ancestry individuals 7,379 European ancestry individuals Illumina [1990000] (imputed) 6 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST007536 Genome-wide genotyping array 2020-02-10 31604244 International Multiple Sclerosis Genetics Consortium 2019-09-01 Science www.ncbi.nlm.nih.gov/pubmed/31604244 Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility. Multiple sclerosis 14,802 European and unknown ancestry cases, 26,703 European and unknown ancestry controls 32,627 European and unknown ancestry cases, 41,672 European and unknown ancestry controls Affymetrix, Illumina [8278136] (imputed) 333 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST009597 Genome-wide genotyping array 2020-04-21 25569235 Demirkan A 2015-01-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25569235 Insight in genome-wide association of metabolite quantitative traits by exome sequence analyses. Serum metabolite levels 2,118 Erasmus Rucphen (founder/genetic isolate) individuals NA Illumina [~ 2500000] (imputed) 9 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST009893 Genome-wide genotyping array 2020-03-02 31361310 Johansson A 2019-07-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31361310 Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema. Allergic rhinitis 18,915 European ancestry cases, 239,773 European ancestry controls NA Affymetrix [15688218] (imputed) 27 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST009719 Genome-wide genotyping array 2020-03-02 31361310 Johansson A 2019-07-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31361310 Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema. Eczema 7,884 European ancestry cases, 239,773 European ancestry controls 21,000 cases, 96,000 controls Affymetrix [15688218] (imputed) 16 Eczema http://purl.obolibrary.org/obo/HP_0000964 GCST009718 Genome-wide genotyping array 2020-03-02 31361310 Johansson A 2019-07-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31361310 Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema. Hay fever and/or eczema 84,034 European ancestry cases, 239,773 European ancestry controls NA Affymetrix [15688218] (imputed) 154 Eczema, allergic rhinitis http://purl.obolibrary.org/obo/HP_0000964, http://www.ebi.ac.uk/efo/EFO_0005854 GCST009717 Genome-wide genotyping array 2020-03-02 31361310 Johansson A 2019-07-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31361310 Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema. Allergic disease (asthma, hay fever or eczema) 106,772 European ancestry cases, 239,773 European ancestry controls 83,335 cases, 34,934 controls Affymetrix [15688218] (imputed) 85 asthma, Eczema, allergic rhinitis http://purl.obolibrary.org/obo/MONDO_0004979, http://purl.obolibrary.org/obo/HP_0000964, http://www.ebi.ac.uk/efo/EFO_0005854 GCST009716 Genome-wide genotyping array 2020-03-02 31361310 Johansson A 2019-07-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31361310 Genome-wide association analysis of 350 000 Caucasians from the UK Biobank identifies novel loci for asthma, hay fever and eczema. Asthma 41,926 European ancestry cases, 239,773 European ancestry controls 10,365 cases, 16,100 controls Affymetrix [15688218] (imputed) 101 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST009720 Genome-wide genotyping array 2020-04-30 26407342 Loukola A 2015-09-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26407342 A Genome-Wide Association Study of a Biomarker of Nicotine Metabolism. Nicotine metabolite ratio in current smokers 1,518 Finnish ancestry individuals NA Illumina [8970401] (imputed) 3 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST009922 Genome-wide genotyping array 2019-04-03 30801121 O'Donnell S 2019-02-25 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/30801121 The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience. Crohn's disease (time to progression) 662 European ancestry individuals NA Illumina [5378266] (imputed) 12 disease progression measurement, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0008336, http://www.ebi.ac.uk/efo/EFO_0000384 GCST007497 Genome-wide genotyping array 2019-04-03 30801121 O'Donnell S 2019-02-25 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/30801121 The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience. Crohn's disease (time to first abdominal surgery) 1,360 European ancestry individuals NA Illumina [5378266] (imputed) 7 disease progression measurement, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0008336, http://www.ebi.ac.uk/efo/EFO_0000384 GCST007498 Genome-wide genotyping array 2019-04-03 30801121 O'Donnell S 2019-02-25 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/30801121 The Unsolved Link of Genetic Markers and Crohn's Disease Progression: A North American Cohort Experience. Crohn's disease (indolent vs progressive) 562 European ancestry individuals with indolent disease, 701 European ancestry individuals with progressive disease NA Illumina [5378266] (imputed) 15 disease progression measurement, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0008336, http://www.ebi.ac.uk/efo/EFO_0000384 GCST007499 Genome-wide genotyping array 2020-09-17 32572135 Zhao Y 2020-06-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32572135 Four Loci Are Associated with Cardiorespiratory Fitness and Endurance Performance in Young Chinese Females. Cardiorespiratory fitness (800m run time) 762 Han Chinese ancestry individuals NA Affymetrix, Illumina [5129327] (imputed) 8 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST010573 Genome-wide genotyping array 2019-02-14 30201983 Tulstrup M 2018-09-10 Leukemia www.ncbi.nlm.nih.gov/pubmed/30201983 NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia. Erythrocyte methylated 6-mercaptopurine metabolite concentration in 6-mercaptopurine-treated acute lymphoblastic leukaemia up to 454 European ancestry individuals NA Illumina [NR] 1 thiopurine metabolite measurement, response to mercaptopurine http://www.ebi.ac.uk/efo/EFO_0009693, http://www.ebi.ac.uk/efo/EFO_0007853 GCST007149 Genome-wide genotyping array 2019-02-14 30201983 Tulstrup M 2018-09-10 Leukemia www.ncbi.nlm.nih.gov/pubmed/30201983 NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia. DNA-incorporated thioguanine levels in 6-mercaptopurine-treated acute lymphoblastic leukaemia 443 European ancestry individuals NA Illumina [NR] 1 thiopurine metabolite measurement, response to mercaptopurine http://www.ebi.ac.uk/efo/EFO_0009693, http://www.ebi.ac.uk/efo/EFO_0007853 GCST007150 Genome-wide genotyping array 2019-02-14 30201983 Tulstrup M 2018-09-10 Leukemia www.ncbi.nlm.nih.gov/pubmed/30201983 NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia. DNA-incorporated thioguanine to erythrocyte thioguanine ratio in 6-mercaptopurine-treated acute lymphoblastic leukaemia up to 443 European ancestry individuals up to 136 European ancestry individuals Illumina [NR] 0 thiopurine metabolite measurement, response to mercaptopurine http://www.ebi.ac.uk/efo/EFO_0009693, http://www.ebi.ac.uk/efo/EFO_0007853 GCST007151 Genome-wide genotyping array 2019-02-14 30201983 Tulstrup M 2018-09-10 Leukemia www.ncbi.nlm.nih.gov/pubmed/30201983 NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia. Erythrocyte thioguanine concentration in 6-mercaptopurine-treated acute lymphoblastic leukaemia 452 European ancestry individuals NA Illumina [NR] 1 thiopurine metabolite measurement, response to mercaptopurine http://www.ebi.ac.uk/efo/EFO_0009693, http://www.ebi.ac.uk/efo/EFO_0007853 GCST007148 Genome-wide genotyping array 2019-09-25 30810208 Nishiyama T 2019-02-22 Sleep www.ncbi.nlm.nih.gov/pubmed/30810208 Genome-wide association meta-analysis and Mendelian randomization analysis confirm ALDH2 influencing on sleep duration in the Japanese population. Sleep duration 31,230 Japanese ancestry individuals 5,140 Japanese ancestry individuals Illumina [5590918] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST008770 Genome-wide genotyping array 2020-06-25 27532455 Sun W 2016-08-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27532455 Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD. Blood protein levels 1,340 European ancestry individuals NA Illumina [NR] 137 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST010104 Genome-wide genotyping array 2019-04-04 30820047 Kunkle BW 2019-02-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30820047 Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Alzheimer's disease (late onset) 21,982 European ancestry cases, 41,944 European ancestry controls up to 13,292 European ancestry cases, up to 17,219 European ancestry controls Affymetrix, Illumina [11480632] (imputed) 24 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST007511 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or hippocampal volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 24,704 European ancestry individuals NA NR [up to 9145464] (imputed) 0 attention deficit hyperactivity disorder, hippocampal volume http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0005035 GCST007587 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or nucleus accumbens volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 11,709 European ancestry individuals NA NR [up to 8615659] (imputed) 0 attention deficit hyperactivity disorder, nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0006931 GCST007583 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or caudate nucleus volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 11,772 European ancestry individuals NA NR [up to 8615485] (imputed) 1 attention deficit hyperactivity disorder, caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004830 GCST007591 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Hippocampal volume 24,704 European ancestry individuals NA NR [9145464] (imputed) 6 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST007590 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Intracranial volume 24,024 European ancestry individuals NA NR [9186920] (imputed) 7 intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0004886 GCST007589 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or intracranial volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 24,024 European ancestry individuals NA NR [up to 9186920] (imputed) 3 attention deficit hyperactivity disorder, intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004886 GCST007586 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or putamen volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 11,646 European ancestry individuals NA NR [up to 8609826] (imputed) 2 attention deficit hyperactivity disorder, putamen volume http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0006932 GCST007582 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or amygdala volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 11,757 European ancestry individuals NA NR [up to 8601199] (imputed) 1 attention deficit hyperactivity disorder, amygdala volume http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0006934 GCST007588 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or pallidum volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 11,640 European ancestry individuals NA NR [~ 8047420] (imputed) 0 attention deficit hyperactivity disorder, pallidum volume http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0006933 GCST007585 Genome-wide genotyping array 2019-04-17 30818988 Klein M 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818988 Genetic Markers of ADHD-Related Variations in Intracranial Volume. Attention deficit hyperactivity disorder or thalamus volume (pleiotropy) 19,099 European ancestry ADHD cases, 1,084 ADHD cases, 34,194 European ancestry controls, 997 controls, 11,694 European ancestry individuals NA NR [~ 8047420] (imputed) 0 attention deficit hyperactivity disorder, thalamus volume http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0006935 GCST007584 Genome-wide genotyping array 2019-10-03 30806694 Walker GJ 2019-02-01 JAMA www.ncbi.nlm.nih.gov/pubmed/30806694 Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease. Thiopurine-induced myelosuppression in inflammatory bowel disease 311 European ancestry cases, 608 European ancestry controls NA NR [6272335] (imputed) 1 myelosuppression, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0007053, http://www.ebi.ac.uk/efo/EFO_0006317 GCST008801 Genome-wide genotyping array 2018-07-20 29787419 Hrdlickova B 2018-05-21 Eur J Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29787419 A locus at 7p14.3 predisposes to refractory celiac disease progression from celiac disease. Refractory celiac disease type II 38 Dutch ancestry cases, 846 Dutch ancestry controls 56 European ancestry cases, 1,285 European ancestry controls Illumina [499626] 2 refractory celiac disease http://www.ebi.ac.uk/efo/EFO_0009266 GCST005928 Genome-wide genotyping array 2019-04-09 30808802 Freidin M 2019-02-26 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30808802 Genome-wide meta-analysis identifies genetic locus on chromosome 9 associated with Modic changes. Modic changes 994 European ancestry cases, 835 European ancestry controls NA Illumina [5479070] (imputed) 10 Modic type vertebral endplate changes http://purl.obolibrary.org/obo/HP_0030775 GCST007537 Genome-wide genotyping array 2019-03-27 30804560 Shrine N 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804560 New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Lung function (FVC) 321,047 European ancestry individuals 79,005 European ancestry individuals Affymetrix [19819130] (imputed) 161 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST007429 Genome-wide genotyping array 2019-03-27 30804560 Shrine N 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804560 New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. FEV1 321,047 European ancestry individuals 79,005 European ancestry individuals Affymetrix [19819130] (imputed) 206 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST007432 Genome-wide genotyping array 2019-03-27 30804560 Shrine N 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804560 New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Lung function (FEV1/FVC) 321,047 European ancestry individuals 79,005 European ancestry individuals Affymetrix [19819130] (imputed) 162 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST007431 Genome-wide genotyping array 2019-03-27 30804560 Shrine N 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804560 New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. Peak expiratory flow 321,047 European ancestry individuals 24,218 European ancestry individuals Affymetrix [19819130] (imputed) 133 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST007430 Genome-wide genotyping array 2019-04-10 30804558 Grove J 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804558 Identification of common genetic risk variants for autism spectrum disorder. Autism spectrum disorder 18,381 European ancestry cases, 27,969 European ancestry controls 2,119 European ancestry cases, 142,379 European ancestry controls Illumina [9112387] (imputed) 46 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST007556 Genome-wide genotyping array 2019-04-10 30804558 Grove J 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804558 Identification of common genetic risk variants for autism spectrum disorder. Autism and major depressive disorder (MTAG) 18,381 European ancestry autism cases, 27,969 European ancestry controls, 111,902 major depression cases, 312,113 controls NA Illumina [NR] (imputed) 8 unipolar depression, autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0003756 GCST007553 Genome-wide genotyping array 2019-04-10 30804558 Grove J 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804558 Identification of common genetic risk variants for autism spectrum disorder. Autism and schizophrenia (MTAG) 18,381 European ancestry autism cases, 27,969 European ancestry controls, 34,129 schizophrenia cases, 45,512 controls NA Illumina [NR] (imputed) 4 autism spectrum disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090 GCST007555 Genome-wide genotyping array 2019-04-10 30804558 Grove J 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804558 Identification of common genetic risk variants for autism spectrum disorder. Autism and educational attainment (MTAG) 18,381 European ancestry autism cases, 27,969 European ancestry controls, 328,917 individuals with educational attainment data NA Illumina [NR] (imputed) 4 autism spectrum disorder, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0003756, http://www.ebi.ac.uk/efo/EFO_0004784 GCST007554 Genome-wide genotyping array 2020-06-03 32193455 Ran S 2020-03-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32193455 Replication of FTO Gene associated with lean mass in a Meta-Analysis of Genome-Wide Association Studies. Lean mass index 2,207 European ancestry individuals 44,296 European ancestry individuals Affymetrix [at least 746709] (imputed) 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST010040 Genome-wide genotyping array 2020-02-05 31666681 Zhao B 2019-10-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31666681 Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). White matter microstructure (mean diusivities) 17,706 European ancestry individuals NA NR [8955960] (imputed) 490 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST009538 Genome-wide genotyping array 2020-02-05 31666681 Zhao B 2019-10-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31666681 Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). White matter microstructure (axial diusivities) 17,706 European ancestry individuals NA NR [8955960] (imputed) 234 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST009537 Genome-wide genotyping array 2020-02-05 31666681 Zhao B 2019-10-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31666681 Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). White matter microstructure (radial diusivities) 17,706 European ancestry individuals NA NR [8955960] (imputed) 517 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST009540 Genome-wide genotyping array 2020-02-05 31666681 Zhao B 2019-10-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31666681 Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). White matter microstructure (mode of anisotropy) 17,706 European ancestry individuals NA NR [8955960] (imputed) 115 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST009536 Genome-wide genotyping array 2020-02-05 31666681 Zhao B 2019-10-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31666681 Large-scale GWAS reveals genetic architecture of brain white matter microstructure and genetic overlap with cognitive and mental health traits (n = 17,706). White matter microstructure (fractional anisotropy) 17,706 European ancestry individuals NA NR [8955960] (imputed) 336 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST009539 Genome-wide genotyping array 2020-06-25 25555482 Gelernter J 2014-09-16 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25555482 Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. Nicotine dependence symptom count 3,529 African American individuals, 4,117 European American individuals NA Illumina [up to 11995908] (imputed) 206 nicotine dependence symptom count http://www.ebi.ac.uk/efo/EFO_0009262 GCST010105 Genome-wide genotyping array 2020-06-17 32180562 Kulyte A 2020-01-25 Mol Metab www.ncbi.nlm.nih.gov/pubmed/32180562 Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort. Spontaneous adipocyte lipolysis 856 European ancestry individuals NA NR [9260588] (imputed) 25 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST010088 Genome-wide genotyping array 2020-06-17 32180562 Kulyte A 2020-01-25 Mol Metab www.ncbi.nlm.nih.gov/pubmed/32180562 Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort. Stimulated adipocyte lipolysis 874 European ancestry individuals NA NR [9260588] (imputed) 41 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST010087 Genome-wide genotyping array 2020-07-21 32193296 Grasby KL 2020-03-01 Science www.ncbi.nlm.nih.gov/pubmed/32193296 The genetic architecture of the human cerebral cortex. Cortical thickness 33,992 European ancestry individuals 14,727 European ancestry individuals, 2,943 individuals Affymetrix, Illumina [NR] 26 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST010281 Genome-wide genotyping array 2020-07-21 32193296 Grasby KL 2020-03-01 Science www.ncbi.nlm.nih.gov/pubmed/32193296 The genetic architecture of the human cerebral cortex. Cortical surface area 33,992 European ancestry individuals 14,727 European ancestry individuals, 2,943 individuals Affymetrix, Illumina [NR] 261 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST010282 Genome-wide genotyping array 2020-07-21 32185793 Yan J 2020-03-17 Clin Genet www.ncbi.nlm.nih.gov/pubmed/32185793 A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels. Follicle stimulating hormone levels 2,590 Han Chinese ancestry individuals NA Affymetrix [3101376] (imputed) 5 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST010265 Genome-wide genotyping array 2020-07-21 32185793 Yan J 2020-03-17 Clin Genet www.ncbi.nlm.nih.gov/pubmed/32185793 A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels. Follicle stimulating hormone in healthy women 708 Han Chinese ancestry individuals NA Affymetrix [3101376] (imputed) 7 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST010264 Genome-wide genotyping array 2020-07-21 32185793 Yan J 2020-03-17 Clin Genet www.ncbi.nlm.nih.gov/pubmed/32185793 A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels. Follicle stimulating hormone levels in polycystic ovary syndrome 1,882 Han Chinese ancestry individuals NA Affymetrix [3101376] (imputed) 4 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST010263 Genome-wide genotyping array 2020-07-21 32185793 Yan J 2020-03-17 Clin Genet www.ncbi.nlm.nih.gov/pubmed/32185793 A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels. Luteinizing hormone levels in polycystic ovary syndrome 1,882 Han Chinese ancestry individuals NA Affymetrix [3101376] (imputed) 0 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST010262 Genome-wide genotyping array 2020-07-21 32185793 Yan J 2020-03-17 Clin Genet www.ncbi.nlm.nih.gov/pubmed/32185793 A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels. Luteinizing hormone levels in healthy women 720 Han Chinese ancestry individuals NA Affymetrix [3101376] (imputed) 1 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST010261 Genome-wide genotyping array 2020-07-21 32185793 Yan J 2020-03-17 Clin Genet www.ncbi.nlm.nih.gov/pubmed/32185793 A genome-wide association study identifies FSHR rs2300441 associated with follicle-stimulating hormone levels. Luteinizing hormone levels 2,590 Han Chinese ancestry individuals NA Affymetrix [3101376] (imputed) 0 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST010260 Genome-wide genotyping array 2020-04-15 32066683 Lacaze P 2020-01-27 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066683 Genetic associations with clozapine-induced myocarditis in patients with schizophrenia. Clozapine-induced myocarditis in schizophrenia 33 cases, 62 controls NA Illumina [6822414] (imputed) 4 myocarditis, response to clozapine http://www.ebi.ac.uk/efo/EFO_0009609, http://purl.obolibrary.org/obo/GO_0097338 GCST009817 Genome-wide genotyping array 2020-07-09 32184442 Olafsdottir T 2020-03-17 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32184442 Genome-wide association identifies seven loci for pelvic organ prolapse in Iceland and the UK Biobank. Pelvic organ prolapse 15,010 European ancestry cases, 340,734 European ancestry controls NA Affymetrix, Illumina [37144863] (imputed) 12 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST010174 Genome-wide genotyping array, Genome-wide sequencing 2020-06-08 32141793 Garman L 2020-03-06 Ocul Immunol Inflamm www.ncbi.nlm.nih.gov/pubmed/32141793 Genome-Wide Association Study of Ocular Sarcoidosis Confirms HLA Associations and Implicates Barrier Function and Autoimmunity in African Americans. Ocular sarcoidosis 260 African American cases, 1,551 African American controls NA Illumina [13976150] (imputed) 84 ocular sarcoidosis http://www.ebi.ac.uk/efo/EFO_0010723 GCST010054 Genome-wide genotyping array 2020-06-08 32141793 Garman L 2020-03-06 Ocul Immunol Inflamm www.ncbi.nlm.nih.gov/pubmed/32141793 Genome-Wide Association Study of Ocular Sarcoidosis Confirms HLA Associations and Implicates Barrier Function and Autoimmunity in African Americans. Ocular sarcoidosis in sarcoidosis 260 African American cases, 513 African American controls NA Illumina [13976150] (imputed) 4 ocular sarcoidosis http://www.ebi.ac.uk/efo/EFO_0010723 GCST010052 Genome-wide genotyping array 2020-06-08 32141793 Garman L 2020-03-06 Ocul Immunol Inflamm www.ncbi.nlm.nih.gov/pubmed/32141793 Genome-Wide Association Study of Ocular Sarcoidosis Confirms HLA Associations and Implicates Barrier Function and Autoimmunity in African Americans. Ocular sarcoidosis 35 European ancestry cases, 2,046 European ancestry controls NA Illumina [4755887] (imputed) 18 ocular sarcoidosis http://www.ebi.ac.uk/efo/EFO_0010723 GCST010053 Genome-wide genotyping array 2020-06-08 32141793 Garman L 2020-03-06 Ocul Immunol Inflamm www.ncbi.nlm.nih.gov/pubmed/32141793 Genome-Wide Association Study of Ocular Sarcoidosis Confirms HLA Associations and Implicates Barrier Function and Autoimmunity in African Americans. Ocular sarcoidosis in sarcoidosis 35 European ancestry cases, 221 European ancestry controls NA Illumina [4755887] (imputed) 2 ocular sarcoidosis http://www.ebi.ac.uk/efo/EFO_0010723 GCST010051 Genome-wide genotyping array 2020-01-29 31844048 Hill WD 2019-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31844048 Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income. Household income (MTAG) 505,541 British and unknown ancestry individuals NA Affymetrix [up to 18485882] (imputed) 343 household income http://www.ebi.ac.uk/efo/EFO_0009695 GCST009524 Genome-wide genotyping array 2020-01-29 31844048 Hill WD 2019-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31844048 Genome-wide analysis identifies molecular systems and 149 genetic loci associated with income. Household income 286,301 British ancestry individuals NA Affymetrix [18485882] (imputed) 68 household income http://www.ebi.ac.uk/efo/EFO_0009695 GCST009523 Genome-wide genotyping array 2018-09-12 29942086 Savage JE 2018-06-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29942086 Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. Intelligence 269,867 European ancestry individuals NA Affymetrix, Illumina [9295118] (imputed) 524 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST006250 Genome-wide genotyping array 2019-03-27 28864454 Lacson JCA 2017-09-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28864454 Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study. Breast cancer (estrogen-receptor positive) 1,325 cases, 1,310 controls NA Illumina [129771] 2 estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_1000649 GCST007415 Exome genotyping array [Exome array] 2019-03-27 28864454 Lacson JCA 2017-09-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28864454 Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study. Breast cancer (estrogen-receptor negative) 212 cases, 1,310 controls NA Illumina [129771] 0 estrogen-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_1000650 GCST007416 Exome genotyping array [Exome array] 2019-03-27 28864454 Lacson JCA 2017-09-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28864454 Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study. Breast cancer (progesterone-receptor positive) 1,049 cases, 1,310 controls NA Illumina [129771] 1 progesterone-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_0009781 GCST007420 Exome genotyping array [Exome array] 2019-03-27 28864454 Lacson JCA 2017-09-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28864454 Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study. Breast cancer (progesterone-receptor negative) 419 cases, 1,310 controls NA Illumina [129771] 0 progesterone-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_0009781 GCST007417 Exome genotyping array [Exome array] 2019-03-27 28864454 Lacson JCA 2017-09-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28864454 Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study. Breast cancer (HER2 positive) 194 cases, 1,310 controls NA Illumina [129771] 0 HER2 Positive Breast Carcinoma http://www.ebi.ac.uk/efo/EFO_1000294 GCST007419 Exome genotyping array [Exome array] 2019-03-27 28864454 Lacson JCA 2017-09-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28864454 Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study. Breast cancer (HER2 negative) 932 cases, 1,310 controls NA Illumina [129771] 0 HER2 negative breast carcinoma http://www.ebi.ac.uk/efo/EFO_0009780 GCST007418 Exome genotyping array [Exome array] 2019-03-27 28864454 Lacson JCA 2017-09-01 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/28864454 Genome-Wide Testing of Exonic Variants and Breast Cancer Risk in the California Teachers Study. Breast cancer 1,704 cases, 1,310 controls NA Illumina [129771] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST007414 Exome genotyping array [Exome array] 2018-12-19 29885931 Langefeld CD 2018-06-06 Kidney Int www.ncbi.nlm.nih.gov/pubmed/29885931 Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions. End stage renal disease x APOL1 genotype interaction 1,749 African American ESRD cases, 901 African American lupus nephritis-ESRD cases NA Illumina [NR] 3 chronic kidney disease, APOL1 risk genotype carrier status http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0009324 GCST006813 Genome-wide genotyping array 2018-12-19 29885931 Langefeld CD 2018-06-06 Kidney Int www.ncbi.nlm.nih.gov/pubmed/29885931 Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions. End stage renal disease in APOL1 risk genotype-negative individuals 945 African American ESRD cases, 988 African American controls, 678 African American lupus nephritis-ESRD cases, 465 African American systemic lupus erythrematosus without nephropathy controls NA Illumina [NR] 2 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST006815 Genome-wide genotyping array 2018-12-19 29885931 Langefeld CD 2018-06-06 Kidney Int www.ncbi.nlm.nih.gov/pubmed/29885931 Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions. End stage renal disease in APOL1 risk genotype-positive individuals 803 African American ESRD cases, 148 African American controls, 223 African American lupus nephritis-ESRD cases, 55 African American systemic lupus erythrematosus without nephropathy controls NA Illumina [NR] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST006816 Genome-wide genotyping array 2018-12-19 29885931 Langefeld CD 2018-06-06 Kidney Int www.ncbi.nlm.nih.gov/pubmed/29885931 Genome-wide association studies suggest that APOL1-environment interactions more likely trigger kidney disease in African Americans with nondiabetic nephropathy than strong APOL1-second gene interactions. End-stage renal disease 1,749 African American ESRD cases, 1,136 African American controls, 901 African American lupus nephritis-ESRD cases, 520 African American systemic lupus erythrematosus without nephropathy controls NA Illumina [NR] 7 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST006814 Genome-wide genotyping array 2020-01-10 31791255 Vicente M 2019-12-02 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/31791255 Population history and genetic adaptation of the Fulani nomads: inferences from genome-wide data and the lactase persistence trait. Lactose tolerance test 53 Fulani individuals, 7 Czech or Slovak individuals NA Illumina [2359821] 2 lactose tolerance test http://www.ebi.ac.uk/efo/EFO_0010557 GCST009418 Genome-wide genotyping array 2018-12-07 29947131 Smit DJA 2018-06-26 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/29947131 Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. Electroencephalogram traits up to 8,425 European and unknown ancestry individuals NA Affymetrix, Illumina, Perlegen [at least 4959085] (imputed) 8 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST006684 Genome-wide genotyping array 2020-01-27 30979435 Lo MT 2019-03-12 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30979435 Identification of genetic heterogeneity of Alzheimer's disease across age. Alzheimer's disease (onset at age over 80) 2,399 European ancestry cases, 4,160 European ancestry controls NA Affymetrix, Illumina [38043082] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009497 Genome-wide genotyping array 2020-01-27 30979435 Lo MT 2019-03-12 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30979435 Identification of genetic heterogeneity of Alzheimer's disease across age. Alzheimer's disease (onset between ages 58 and 79) 7,316 European ancestry cases, 7,579 European ancestry controls NA Affymetrix, Illumina [38043082] (imputed) 28 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009496 Genome-wide genotyping array 2018-10-17 29942513 Penney ME 2018-06-13 Biomark Res www.ncbi.nlm.nih.gov/pubmed/29942513 Associations of single nucleotide polymorphisms with mucinous colorectal cancer: genome-wide common variant and gene-based rare variant analyses. Mucinous adenocarcinoma in colorectal cancer 57 European ancestry cases, 448 European ancestry controls NA Illumina [729373] 17 colorectal mucinous adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0009361 GCST006411 Genome-wide genotyping array 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Basophil count 5,578 European ancestry individuals NA NR [16536512] (imputed) 2 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST010240 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Eosinophil counts 5,586 European ancestry individuals NA NR [16536512] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST010239 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Hemoglobin 4,221 European ancestry individuals NA NR [16536512] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST010238 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Hematocrit 2,096 European ancestry individuals NA NR [16536512] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST010237 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Lymphocyte count 5,614 European ancestry individuals NA NR [16536512] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST010236 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Mean corpuscular hemoglobin 6,883 European ancestry individuals NA NR [16536512] (imputed) 2 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST010235 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Mean corpuscular hemoglobin concentration 6,891 European ancestry individuals NA NR [16536512] (imputed) 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST010234 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Mean corpuscular volume 6,891 European ancestry individuals NA NR [16536512] (imputed) 1 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST010233 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Monocyte count 5,533 European ancestry individuals NA NR [16536512] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST010232 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Mean platelet volume 6,228 European ancestry individuals NA NR [16536512] (imputed) 6 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST010231 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Neutrophil count 2,080 European ancestry individuals NA NR [16536512] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST010230 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Platelet count 2,083 European ancestry individuals NA NR [16536512] (imputed) 4 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST010229 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. Red blood cell count 7,113 European ancestry individuals NA NR [16536512] (imputed) 1 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST010228 Genome-wide genotyping array, Genome-wide sequencing 2020-07-20 28031487 Guo MH 2016-12-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28031487 Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms. White blood cell count 7,116 European ancestry individuals NA NR [16536512] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST010227 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 30801552 Oetting WS 2019-02-19 Transplantation www.ncbi.nlm.nih.gov/pubmed/30801552 Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies. Tacrolimus trough concentration in kidney transplant patients 1,363 European ancestry individuals, 299 African American individuals 609 European ancestry individuals, 171 African American individuals Affymetrix [~ 40000000] (imputed) 4 tacrolimus measurement http://www.ebi.ac.uk/efo/EFO_0008458 GCST008577 Genome-wide genotyping array 2019-09-02 30801552 Oetting WS 2019-02-19 Transplantation www.ncbi.nlm.nih.gov/pubmed/30801552 Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies. Nephrotoxicity in tacrolimus-treated kidney transplant patients (time to event) 1,352 European ancestry individuals 609 European ancestry individuals Affymetrix [~ 40000000] (imputed) 0 renal system measurement, Acute kidney injury, response to tacrolimus http://www.ebi.ac.uk/efo/EFO_0004742, http://purl.obolibrary.org/obo/HP_0001919, http://www.ebi.ac.uk/efo/EFO_0010052 GCST008582 Genome-wide genotyping array 2019-09-02 30801552 Oetting WS 2019-02-19 Transplantation www.ncbi.nlm.nih.gov/pubmed/30801552 Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies. Nephrotoxicity in cyclosporine-treated kidney transplant patients (time to event) 475 European ancestry individuals 63 European ancestry individuals Affymetrix [~ 40000000] (imputed) 0 renal system measurement, response to cyclosporine, Acute kidney injury http://www.ebi.ac.uk/efo/EFO_0004742, http://www.ebi.ac.uk/efo/EFO_0010053, http://purl.obolibrary.org/obo/HP_0001919 GCST008581 Genome-wide genotyping array 2019-09-02 30801552 Oetting WS 2019-02-19 Transplantation www.ncbi.nlm.nih.gov/pubmed/30801552 Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies. Anemia in mycophenolic acid treated kidney transplant patients (time to event) 1,785 European ancestry individuals 438 European ancestry individuals Affymetrix [~ 40000000] (imputed) 0 anemia (phenotype), response to mycophenolic acid http://www.ebi.ac.uk/efo/EFO_0004272, http://www.ebi.ac.uk/efo/EFO_0010054 GCST008580 Genome-wide genotyping array 2019-09-02 30801552 Oetting WS 2019-02-19 Transplantation www.ncbi.nlm.nih.gov/pubmed/30801552 Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies. Leukopenia in mycophenolic acid treated kidney transplant patients (time to event) 1,785 European ancestry individuals, 338 African American individuals 657 European ancestry individuals, 171 African American individuals Affymetrix [~ 40000000] (imputed) 0 leukopenia, response to mycophenolic acid http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0010054 GCST008579 Genome-wide genotyping array 2019-09-02 30801552 Oetting WS 2019-02-19 Transplantation www.ncbi.nlm.nih.gov/pubmed/30801552 Genetic Variants Associated with Immunosuppressant Pharmacokinetics and Adverse Effects in the DeKAF Genomics Genome Wide Association Studies. New onset diabetes in calcineurin inhibitor treated kidney transplant patients (time to event) 1,235 European ancestry individuals, 256 African American individuals 487 European ancestry individuals, 94 African American individuals Affymetrix [~ 40000000] (imputed) 0 response to calcineurin inhibitor, diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0010055, http://www.ebi.ac.uk/efo/EFO_0000400 GCST008578 Genome-wide genotyping array 2019-03-19 30823506 Hong EP 2019-02-25 J Clin Med www.ncbi.nlm.nih.gov/pubmed/30823506 Genomic Variations in Susceptibility to Intracranial Aneurysm in the Korean Population. Intracranial aneurysm 250 Korean ancestry cases, 296 Korean ancestry controls NA Affymetrix [508192] 29 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST007354 Genome-wide genotyping array 2020-07-08 32024964 Gonzalez-Serna D 2020-02-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32024964 A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn's disease. Crohn's disease or systemic sclerosis 2,281 European ancestry systemic sclerosis cases, 1,988 European ancestry Crohn’s disease cases, 7,388 European ancestry controls 3,453 European ancestry systemic sclerosis cases, 2,600 European ancestry Crohn’s disease cases, 7,180 European ancestry controls Illumina [5994231] (imputed) 4 systemic scleroderma, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000717, http://www.ebi.ac.uk/efo/EFO_0000384 GCST010124 Genome-wide genotyping array 2019-03-25 30804566 Lane JM 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804566 Biological and clinical insights from genetics of insomnia symptoms. Insomnia symptoms (never/rarely vs. sometimes/usually) 345,022 European ancestry cases, 108,357 European ancestry controls 17,140 European ancestry cases, 61,850 European ancestry controls Affymetrix [14661600] (imputed) 49 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST007387 Genome-wide genotyping array 2019-03-25 30804566 Lane JM 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804566 Biological and clinical insights from genetics of insomnia symptoms. Insomnia symptoms (never/rarely vs. usually) 129,270 European ancestry cases, 108,357 European ancestry controls 17,140 European ancestry cases, 61,850 European ancestry controls Affymetrix [14661600] (imputed) 55 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST007388 Genome-wide genotyping array 2019-05-01 30804561 Sakornsakolpat P 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804561 Genetic landscape of chronic obstructive pulmonary disease identifies heterogeneous cell-type and phenotype associations. Chronic obstructive pulmonary disease 35,735 cases, 222,076 controls NA Affymetrix, Illumina [6224355] (imputed) 124 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST007692 Genome-wide genotyping array 2020-05-29 32126890 Ter Hark SE 2020-03-04 J Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/32126890 A new genetic locus for antipsychotic-induced weight gain: A genome-wide study of first-episode psychosis patients using amisulpride (from the OPTiMiSE cohort). Weight gain in amisulpride-treated first-episode psychosis 184 European ancestry individuals, 9 African ancestry individuals, 6 Hispanic/Latin American individuals, 3 South Asian ancestry individuals, 2 East Asian ancestry individuals, 2 individuals NA Illumina [4533042] (imputed) 21 longitudinal BMI measurement, response to amisulpride http://www.ebi.ac.uk/efo/EFO_0005937, http://www.ebi.ac.uk/efo/EFO_0010718 GCST010007 Genome-wide genotyping array 2019-03-10 30818990 Yu D 2019-03-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30818990 Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. Tourette syndrome 4,271 European ancestry cases, 548 European ancestry cases from 207 families, 9,488 European ancestry controls 706 Icelandic ancestry cases, 6,068 Icelandic ancestry controls Illumina [8265319] (imputed) 24 Tourette syndrome http://www.ebi.ac.uk/efo/EFO_0004895 GCST007277 Genome-wide genotyping array 2019-03-22 30807572 Gong J 2019-02-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30807572 Genetic association and transcriptome integration identify contributing genes and tissues at cystic fibrosis modifier loci. Meconium ileus in cystic fibrosis 1,115 European ancestry cases, 5,655 European ancestry controls NA Illumina [8763019] (imputed) 7 cystic fibrosis associated meconium ileus http://www.ebi.ac.uk/efo/EFO_0004608 GCST007367 Genome-wide genotyping array, Genome-wide sequencing 2022-09-21 32035127 Bye A 2020-02-05 Prog Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/32035127 Identification of novel genetic variants associated with cardiorespiratory fitness. Maximal oxygen uptake response 3,470 European ancestry individuals 718 European ancestry individuals Illumina [123545] 0 maximal oxygen uptake measurement http://www.ebi.ac.uk/efo/EFO_0004887 GCST012960 Genome-wide genotyping array 2020-02-27 27352405 Balakrishnan P 2016-06-28 Environ Health Perspect www.ncbi.nlm.nih.gov/pubmed/27352405 Association of Cardiometabolic Genes with Arsenic Metabolism Biomarkers in American Indian Communities: The Strong Heart Family Study (SHFS). Arsenic metabolism 2,428 American Indian ancestry individuals NA Illumina [120975] 5 urinary arsenic measurement http://www.ebi.ac.uk/efo/EFO_0004880 GCST009703 Targeted genotyping array [Cardio-MetaboChip] 2021-08-13 32889700 Qin N 2020-09-05 Front Med www.ncbi.nlm.nih.gov/pubmed/32889700 Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma. Lung adenocarcinoma 15,581 Chinese or European ancestry cases, 27,355 Chinese or European ancestry controls NA NR [NR] (imputed) 23 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST012201 Genome-wide genotyping array 2021-08-13 32889700 Qin N 2020-09-05 Front Med www.ncbi.nlm.nih.gov/pubmed/32889700 Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma. Squamous cell lung carcinoma 8,350 Chinese or European ancestry cases, 27,355 Chinese or European ancestry controls NA NR [NR] (imputed) 13 squamous cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000708 GCST012200 Genome-wide genotyping array 2021-08-13 32889700 Qin N 2020-09-05 Front Med www.ncbi.nlm.nih.gov/pubmed/32889700 Comprehensive functional annotation of susceptibility variants identifies genetic heterogeneity between lung adenocarcinoma and squamous cell carcinoma. Non-small cell lung cancer 27,120 Chinese or European ancestry cases, 27,355 Chinese or European ancestry controls NA NR [NR] (imputed) 28 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST012199 Genome-wide genotyping array 2020-04-17 32141789 Theriault S 2019-10-15 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32141789 Genetic Association Analyses Highlight IL6, ALPL, and NAV1 As 3 New Susceptibility Genes Underlying Calcific Aortic Valve Stenosis. Calcific aortic valve stenosis 5,115 European ancestry cases, 354,072 European ancestry controls NA Affymetrix, Illumina [8000000] (imputed) 26 aortic stenosis, aortic valve calcification http://www.ebi.ac.uk/efo/EFO_0000266, http://www.ebi.ac.uk/efo/EFO_0005239 GCST009870 Genome-wide genotyping array 2020-05-04 32232851 Deguchi H 2020-03-30 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/32232851 Novel exomic rare variants associated with venous thrombosis. Venous thromboembolism 104 European ancestry cases, 211 European ancestry controls NA Illumina [308166] 22 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST009936 Exome genotyping array [Exome array] 2018-09-20 30019117 Liu J 2018-07-17 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30019117 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. Adolescent idiopathic scoliosis 196 cases, 303 controls NA Affymetrix [NR] 1317 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST006287 Genome-wide genotyping array 2019-06-25 30804565 Jansen PR 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804565 Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. Insomnia 651,923 European ancestry males, 679,087 European ancestry females NA Affymetrix, Illumina [NR] (imputed) 364 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST007988 Genome-wide genotyping array 2019-06-25 30804565 Jansen PR 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804565 Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. Morningness 434,835 European ancestry individuals NA Affymetrix, Illumina [11597492] (imputed) 274 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST007983 Genome-wide genotyping array 2019-06-25 30804565 Jansen PR 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804565 Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. Sleep duration 384,317 European ancestry individuals NA Affymetrix, Illumina [10862567] (imputed) 53 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST007982 Genome-wide genotyping array 2019-06-25 30804565 Jansen PR 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804565 Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. Ease of getting up in the morning 385,949 European ancestry individuals NA Affymetrix, Illumina [10862568] (imputed) 70 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST007986 Genome-wide genotyping array 2019-06-25 30804565 Jansen PR 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804565 Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. Daytime nap 386,577 European ancestry individuals NA Affymetrix, Illumina [10858887] (imputed) 7 daytime rest measurement http://www.ebi.ac.uk/efo/EFO_0007828 GCST007987 Genome-wide genotyping array 2019-06-25 30804565 Jansen PR 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804565 Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. Daytime sleepiness 386,548 European ancestry individuals NA Affymetrix, Illumina [10820725] (imputed) 1 excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0007875 GCST007984 Genome-wide genotyping array 2019-06-25 30804565 Jansen PR 2019-02-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30804565 Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways. Snoring 359,916 European ancestry individuals NA Affymetrix, Illumina [10862568] (imputed) 42 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST007985 Genome-wide genotyping array 2020-04-17 32117775 Wu J 2020-02-11 Front Oncol www.ncbi.nlm.nih.gov/pubmed/32117775 The Rare Variant rs35356162 in UHRF1BP1 Increases Bladder Cancer Risk in Han Chinese Population. Bladder cancer 995 Han Chinese ancestry cases, 1,008 Han Chinese ancestry controls 2,404 Han Chinese ancestry cases, 3,639 Han Chinese ancestry controls Illumina [270241] 2 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST009872 Exome genotyping array [Exome array] 2021-04-30 32132452 Jin EH 2020-03-01 Clin Transl Gastroenterol www.ncbi.nlm.nih.gov/pubmed/32132452 A Novel Susceptibility Locus Near GRIK2 Associated With Erosive Esophagitis in a Korean Cohort. Erosive esophagitis 493 Korean ancestry male cases, 123 Korean ancestry female cases, 1,777 Korean ancestry male controls, 1,227 Korean ancestry female controls 100 Korean ancestry male cases, 32 Korean ancestry female cases, 297 Korean ancestry male controls, 193 Korean ancestry female controls Affymetrix [3693205] (imputed) 0 peptic esophagitis http://www.ebi.ac.uk/efo/EFO_1001095 GCST011585 Genome-wide genotyping array 2019-04-03 30809046 Schmitz B 2019-02-26 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30809046 Genome-wide association study suggests impact of chromosome 10 rs139401390 on kidney function in patients with coronary artery disease. Estimated glomerular filtration rate in coronary artery disease and impaired kidney function 499 European ancestry cases 574 European ancestry cases Affymetrix [> 10000000] (imputed) 2 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST007495 Genome-wide genotyping array 2020-04-17 32133506 Li H 2020-03-05 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/32133506 Genome-wide Association Study of Creativity Reveals Genetic Overlap With Psychiatric Disorders, Risk Tolerance, and Risky Behaviors. Creativity 4,664 Han Chinese ancestry individuals NA Illumina [up to 5481607] (imputed) 7 creativity measurement http://www.ebi.ac.uk/efo/EFO_0010650 GCST009844 Genome-wide genotyping array 2019-03-27 30824882 Gunjaca I 2019-03-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30824882 Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population. Thyroxine levels 1,121 Croatian ancestry individuals NA NR [7597900] (imputed) 1 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST007428 Genome-wide genotyping array 2019-03-27 30824882 Gunjaca I 2019-03-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30824882 Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population. Triiodothyronine levels 623 Croatian ancestry individuals NA NR [8753628] (imputed) 3 triiodothyronine measurement http://www.ebi.ac.uk/efo/EFO_0008392 GCST007426 Genome-wide genotyping array 2019-03-27 30824882 Gunjaca I 2019-03-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30824882 Genome-wide association meta-analysis for total thyroid hormone levels in Croatian population. Triiodothyronine/thyroxine ratio 623 Croatian ancestry individuals NA NR [8752746] (imputed) 3 tri-iodothyronine/thyroxine ratio measurement http://www.ebi.ac.uk/efo/EFO_0009779 GCST007427 Genome-wide genotyping array 2020-06-04 32296059 Han Y 2020-04-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32296059 Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma. Asthma 84,492 European ancestry cases, 2,149 African American cases, 606 Hispanic cases, 1,239 Japanese ancestry cases, 437,036 European ancestry controls, 6,055 African American controls, 792 Hispanic controls, 3,976 Japanese ancestry controls NR NR [> 9500000] (imputed) 167 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST010043 Genome-wide genotyping array 2020-06-04 32296059 Han Y 2020-04-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32296059 Genome-wide analysis highlights contribution of immune system pathways to the genetic architecture of asthma. Asthma 64,538 European ancestry cases, 239,321 European ancestry controls NR NR [9572556] (imputed) 145 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST010042 Genome-wide genotyping array 2020-10-15 32289280 Zhang Y 2020-04-11 Am J Obstet Gynecol www.ncbi.nlm.nih.gov/pubmed/32289280 A genome-wide association study of polycystic ovary syndrome identified from electronic health records. Polycystic ovary syndrome 1,735 European ancestry cases, 1,007 European, African American and unknown ancestry cases, 27,812 European ancestry controls, 23,626 European, African American and unknown ancestry controls 253 European ancestry cases, 2,161 European ancestry controls NR [at least 5648769] (imputed) 5 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST010687 Genome-wide genotyping array 2020-07-08 32382064 Pirruccello JP 2020-05-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32382064 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Left ventricular end-diastolic volume 35,407 European ancestry individuals, 95 African ancestry individuals, 108 East Asian ancestry individuals, 303 South Asian ancestry individuals, 128 individuals 940 European ancestry individuals, 299 East Asian ancestry individuals, 507 African American individuals, 438 Hispanic individuals Affymetrix [13660711] (imputed) 2 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST010131 Genome-wide genotyping array 2020-07-08 32382064 Pirruccello JP 2020-05-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32382064 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Left ventricular end-systolic volume 35,407 European ancestry individuals, 95 African ancestry individuals, 108 East Asian ancestry individuals, 303 South Asian ancestry individuals, 128 individuals 940 European ancestry individuals, 299 East Asian ancestry individuals, 507 African American individuals, 438 Hispanic individuals Affymetrix [13660711] (imputed) 3 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST010130 Genome-wide genotyping array 2020-07-08 32382064 Pirruccello JP 2020-05-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32382064 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Left ventricular stroke volume 35,407 European ancestry individuals, 95 African ancestry individuals, 108 East Asian ancestry individuals, 303 South Asian ancestry individuals, 128 individuals 940 European ancestry individuals, 299 East Asian ancestry individuals, 507 African American individuals, 438 Hispanic individuals Affymetrix [13660711] (imputed) 0 left ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0010555 GCST010129 Genome-wide genotyping array 2020-07-08 32382064 Pirruccello JP 2020-05-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32382064 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Body surface area-indexed left ventricular end-diastolic volume 35,407 European ancestry individuals, 95 African ancestry individuals, 108 East Asian ancestry individuals, 303 South Asian ancestry individuals, 128 individuals 940 European ancestry individuals, 299 East Asian ancestry individuals, 507 African American individuals, 438 Hispanic individuals Affymetrix [13660711] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST010128 Genome-wide genotyping array 2020-07-08 32382064 Pirruccello JP 2020-05-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32382064 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Body surface area-indexed left ventricular end-systolic volume 35,407 European ancestry individuals, 95 African ancestry individuals, 108 East Asian ancestry individuals, 303 South Asian ancestry individuals, 128 individuals 940 European ancestry individuals, 299 East Asian ancestry individuals, 507 African American individuals, 438 Hispanic individuals Affymetrix [13660711] (imputed) 0 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST010127 Genome-wide genotyping array 2020-07-08 32382064 Pirruccello JP 2020-05-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32382064 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Body surface area-indexed left ventricular stroke volume 35,407 European ancestry individuals, 95 African ancestry individuals, 108 East Asian ancestry individuals, 303 South Asian ancestry individuals, 128 individuals 940 European ancestry individuals, 299 East Asian ancestry individuals, 507 African American individuals, 438 Hispanic individuals Affymetrix [13660711] (imputed) 0 left ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0010555 GCST010126 Genome-wide genotyping array 2020-07-08 32382064 Pirruccello JP 2020-05-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32382064 Analysis of cardiac magnetic resonance imaging in 36,000 individuals yields genetic insights into dilated cardiomyopathy. Left ventricular ejection fraction 35,407 European ancestry individuals, 95 African ancestry individuals, 108 East Asian ancestry individuals, 303 South Asian ancestry individuals, 128 individuals 940 European ancestry individuals, 299 East Asian ancestry individuals, 507 African American individuals, 438 Hispanic individuals Affymetrix [13660711] (imputed) 4 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST010125 Genome-wide genotyping array 2020-08-03 32373937 Dardani C 2020-05-06 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/32373937 Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian-randomization study. Cleft lip with or without cleft palate 1,692 European ancestry cases, 4,259 European ancestry controls NA NR [7618724] (imputed) 9 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST010379 Genome-wide genotyping array 2020-04-29 26690388 Tang CS 2015-12-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26690388 Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese. LDL cholesterol levels 12,685 Chinese ancestry individuals NA Illumina [286795] 5 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST009917 Exome genotyping array [Exome array] 2020-04-29 26690388 Tang CS 2015-12-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26690388 Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese. HDL cholesterol levels 12,685 Chinese ancestry individuals NA Illumina [286795] 7 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST009918 Exome genotyping array [Exome array] 2020-04-29 26690388 Tang CS 2015-12-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26690388 Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese. Total cholesterol levels 12,685 Chinese ancestry individuals NA Illumina [286795] 5 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST009919 Exome genotyping array [Exome array] 2020-04-29 26690388 Tang CS 2015-12-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26690388 Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese. Total triglycerides levels 12,685 Chinese ancestry individuals NA Illumina [286795] 7 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST009920 Exome genotyping array [Exome array] 2020-06-03 32119686 Dahlin A 2020-03-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/32119686 Genome-wide interaction study reveals age-dependent determinants of responsiveness to inhaled corticosteroids in individuals with asthma. Adverse response to inhaled corticosteroid treatment x age interaction in asthma 407 European ancestry cases, 376 European ancestry controls 287 European ancestry cases, 251 European ancestry controls Affymetrix, Illumina [8589102] (imputed) 17 response to corticosteroid, age at assessment http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0008007 GCST010039 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse triple positive glioma (IDH and TERT mutations, 1p19q codeletion) 189 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 138 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 3 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST011000 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse glioma (IDH mutation) 622 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 390 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 8 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST011004 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse glioma (IDH wildtype) 698 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 409 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 2 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST011003 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse glioma (IDH mutation, 1p/19q codeletion) 245 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 145 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 2 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST011002 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse glioma (IDH mutation, 1p/19q non-codeleted) 316 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 245 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 4 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST011001 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse glioma (IDH and TERT mutations) 39 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 13 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 0 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST010999 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse glioma (IDH mutation only) 241 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 214 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 2 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST010998 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse glioma (TERT mutation only) 419 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 159 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 2 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST010997 Genome-wide genotyping array 2021-01-27 32386320 Eckel-Passow JE 2020-05-09 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/32386320 Adult Diffuse Glioma GWAS by Molecular Subtype Identifies Variants in D2HGDH and FAM20C. Adult diffuse triple negative glioma (IDH and TERT wildtype, 1p/19q non-codeleted) 87 European and unknown ancestry cases, 1,889 European and unknown ancestry controls 33 European and unknown ancestry cases, 808 European and unknown ancestry controls Illumina [NR] (imputed) 0 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST010996 Genome-wide genotyping array 2021-05-19 32123936 Shiota M 2020-03-02 Cancer Immunol Immunother www.ncbi.nlm.nih.gov/pubmed/32123936 Genome-wide association study of genetic variations associated with treatment failure after intravesical bacillus Calmette-Guérin therapy for non-muscle invasive bladder cancer. treatment failure in response to intravesical BCG therapy in non-muscle invasive bladder cancer 44 Japanese ancestry individuals 47 Japanese ancestry individuals NR [657429] 0 response to BCG intravesical immunotherapy http://www.ebi.ac.uk/efo/EFO_0011041 GCST011697 Genome-wide genotyping array 2020-07-09 32118827 Bonde A 2020-02-28 J Trauma Acute Care Surg www.ncbi.nlm.nih.gov/pubmed/32118827 Identification of a new genetic variant associated with cholecystitis: a multicenter genome-wide association study. Acute cholecystitis 900 European ancestry cases, 23,727 European ancestry controls NA Illumina [NR] (imputed) 1 Cholecystitis, Acute http://www.ebi.ac.uk/efo/EFO_1001289 GCST010176 Genome-wide genotyping array 2020-07-09 32118827 Bonde A 2020-02-28 J Trauma Acute Care Surg www.ncbi.nlm.nih.gov/pubmed/32118827 Identification of a new genetic variant associated with cholecystitis: a multicenter genome-wide association study. Cholelithiasis up to 2,377 European ancestry cases, 22,203 European ancestry controls NA Illumina [NR] (imputed) 0 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST010177 Genome-wide genotyping array 2020-07-09 32117412 Boua PR 2020-02-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/32117412 Novel and Known Gene-Smoking Interactions With cIMT Identified as Potential Drivers for Atherosclerosis Risk in West-African Populations of the AWI-Gen Study. Carotid intima media thickness x smoking interaction 465 West African ancestry male smokers, 1,311 West African ancestry male non-smokers NA Illumina [7839440] (imputed) 32 smoking status measurement, carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0007117 GCST010151 Genome-wide genotyping array 2020-07-22 32279069 Rovira P 2020-04-12 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/32279069 Shared genetic background between children and adults with attention deficit/hyperactivity disorder. Attention deficit hyperactivity disorder 17,149 European ancestry cases, 32,411 European ancestry controls NA Illumina [~ 1092418] (imputed) 7 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010291 Genome-wide genotyping array 2020-07-22 32279069 Rovira P 2020-04-12 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/32279069 Shared genetic background between children and adults with attention deficit/hyperactivity disorder. Attention deficit hyperactivity disorder (persistent) 6,532 European ancestry cases, 15,874 European ancestry controls NA Illumina [~ 1113287] (imputed) 25 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010290 Genome-wide genotyping array 2020-07-22 32279069 Rovira P 2020-04-12 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/32279069 Shared genetic background between children and adults with attention deficit/hyperactivity disorder. Attention deficit hyperactivity disorder (childhood) 10,617 European ancestry cases, 16,537 European ancestry controls NA Illumina [~ 1072558] (imputed) 10 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010289 Genome-wide genotyping array 2020-06-12 26838040 Kristjansson RP 2016-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26838040 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase. Lactate dehydrogenase levels 98,585 Icelandic ancestry individuals NA Illumina [28300000] (imputed) 15 L lactate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0004808 GCST010069 Genome-wide genotyping array 2020-06-12 26838040 Kristjansson RP 2016-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26838040 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase. Creatine kinase levels 63,159 Icelandic ancestry individuals NA Illumina [28300000] (imputed) 11 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST010070 Genome-wide genotyping array 2020-06-12 26838040 Kristjansson RP 2016-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26838040 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase. Creatine kinase levels in statin users 5,207 Icelandic ancestry individuals NA Illumina [28300000] (imputed) 3 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST010068 Genome-wide genotyping array 2020-06-12 26838040 Kristjansson RP 2016-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26838040 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase. Creatine kinase levels in off-statin users 6,877 Icelandic ancestry individuals NA Illumina [28300000] (imputed) 3 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST010067 Genome-wide genotyping array 2020-06-12 26838040 Kristjansson RP 2016-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26838040 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase. Lactate dehydrogenase levels in statin users 6,266 Icelandic ancestry individuals NA Illumina [28300000] (imputed) 2 L lactate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0004808 GCST010066 Genome-wide genotyping array 2020-06-12 26838040 Kristjansson RP 2016-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26838040 Common and rare variants associating with serum levels of creatine kinase and lactate dehydrogenase. Lactate dehydrogenase levels in off-statin users 6,877 Icelandic ancestry individuals NA Illumina [28300000] (imputed) 5 L lactate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0004808 GCST010065 Genome-wide genotyping array 2020-04-17 32109421 Li C 2020-02-20 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32109421 Genome-Wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length. Leukocyte telomere length 78,592 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 30071938] (imputed) 49 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST009856 Genome-wide genotyping array 2020-06-02 32186652 Chen HY 2020-03-18 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/32186652 Association of FADS1/2 Locus Variants and Polyunsaturated Fatty Acids With Aortic Stenosis. Aortic valve stenosis 3,469 European ancestry cases, 41,234 European ancestry controls 3,751 European ancestry cases, 236,142 European ancestry controls, 2,175 cases, 25,347 controls Affymetrix [615643] 1 aortic stenosis http://www.ebi.ac.uk/efo/EFO_0000266 GCST010038 Genome-wide genotyping array 2020-06-25 25590795 Yazar S 2015-04-01 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/25590795 Genetic and environmental factors in conjunctival UV autofluorescence. Conjunctival UV autofluorescence (CUVAF) 1,251 European ancestry individuals NA Illumina [5003381] (imputed) 5 eye measurement, sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0004731, http://www.ebi.ac.uk/efo/EFO_0010729 GCST010106 Genome-wide genotyping array 2020-04-24 32108986 Price KM 2020-02-27 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/32108986 Genome-Wide Association Study of Word Reading: Overlap with Risk Genes for Neurodevelopmental Disorders. Reading disability 4,494 European ancestry cases, 306 European ancestry siblings NA Illumina [5300000] (imputed) 7 dyslexia http://www.ebi.ac.uk/efo/EFO_0005424 GCST009897 Genome-wide genotyping array 2020-05-28 32009195 Condreay LD 2020-02-03 Rheumatol Int www.ncbi.nlm.nih.gov/pubmed/32009195 Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis. Frequency of relapse in mepolizumab-treated eosinophilic granulomatosis with polyangiitis 61 individuals NA Affymetrix [7154205] (imputed) 2 response to mepolizumab, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0008459, http://www.ebi.ac.uk/efo/EFO_0008336 GCST009999 Genome-wide genotyping array 2020-05-28 32009195 Condreay LD 2020-02-03 Rheumatol Int www.ncbi.nlm.nih.gov/pubmed/32009195 Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis. Average oral glucocorticoid dose in mepolizumab-treated eosinophilic granulomatosis with polyangiitis 61 individuals NA Affymetrix [7154205] (imputed) 12 response to mepolizumab, Glucocorticoid use measurement http://www.ebi.ac.uk/efo/EFO_0008459, http://www.ebi.ac.uk/efo/EFO_0009942 GCST009998 Genome-wide genotyping array 2020-05-28 32009195 Condreay LD 2020-02-03 Rheumatol Int www.ncbi.nlm.nih.gov/pubmed/32009195 Pharmacogenetic investigation of efficacy response to mepolizumab in eosinophilic granulomatosis with polyangiitis. Accrued duration of remission in mepolizumab-treated eosinophilic granulomatosis with polyangiitis 61 individuals NA Affymetrix [7154205] (imputed) 14 disease free survival, response to mepolizumab http://www.ebi.ac.uk/efo/EFO_0000409, http://www.ebi.ac.uk/efo/EFO_0008459 GCST010000 Genome-wide genotyping array 2020-04-21 32107650 Liu L 2020-02-27 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/32107650 A trans-ethnic two-stage polygenetic scoring analysis detects genetic correlation between osteoporosis and schizophrenia. Schizophrenia (MTAG) 1,627 Han Chinese ancestry individuals with osteoporosis-related bone measurements, 1,475 Han Chinese ancestry schizophrenia cases, 1,022 Han Chinese ancestry schizophrenia controls NA Affymetrix [NR] 4 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST009891 Genome-wide genotyping array 2020-04-21 32107650 Liu L 2020-02-27 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/32107650 A trans-ethnic two-stage polygenetic scoring analysis detects genetic correlation between osteoporosis and schizophrenia. Osteoporosis-related phenotypes (MTAG) 1,627 Han Chinese ancestry individuals with osteoporosis-related bone measurements, 1,475 Han Chinese ancestry schizophrenia cases, 1,022 Han Chinese ancestry schizophrenia controls NA Affymetrix [NR] 7 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST009892 Genome-wide genotyping array 2020-04-17 32099098 Polimanti R 2020-02-26 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32099098 Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Opioid dependence in opioid exposure 1,231 African ancestry cases, 3,272 European ancestry cases, 1,297 African ancestry controls, 2,876 European ancestry controls NA NR [up to 8956178] (imputed) 0 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST009854 Genome-wide genotyping array 2020-04-17 32099098 Polimanti R 2020-02-26 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32099098 Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Opioid dependence 1,027 African ancestry cases, 3,211 European ancestry cases, 6,111 African ancestry controls, 11,589 European ancestry controls NA NR [up to 8896928] (imputed) 1 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST009853 Genome-wide genotyping array 2020-04-17 32099098 Polimanti R 2020-02-26 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32099098 Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium. Opioid exposure 1,297 African ancestry cases, 2,876 European ancestry cases, 7,063 African ancestry controls, 25,437 European ancestry controls NA NR [up to 9065342] (imputed) 3 Opioid use measurement http://www.ebi.ac.uk/efo/EFO_0009937 GCST009852 Genome-wide genotyping array 2020-05-21 31969693 Coleman JRI 2020-01-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31969693 Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Major depressive disorder 29,475 European ancestry cases, 63,482 European ancestry controls NA Affymetrix [7791636] (imputed) 67 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST009979 Genome-wide genotyping array 2020-05-21 31969693 Coleman JRI 2020-01-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31969693 Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Major depressive disorder in trauma exposed individuals 13,393 European ancestry cases, 10,701 European ancestry controls Affymetrix [7791636] (imputed) 21 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST009980 Genome-wide genotyping array 2020-05-21 31969693 Coleman JRI 2020-01-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31969693 Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Major depressive disorder in trauma-unexposed individuals 9,487 European ancestry cases, 39,677 European ancestry controls NA Affymetrix [7791636] (imputed) 27 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST009981 Genome-wide genotyping array 2020-05-21 31969693 Coleman JRI 2020-01-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31969693 Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Trauma exposure 35,269 European ancestry cases, 63,451 European ancestry controls NA Affymetrix [7791636] (imputed) 88 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST009982 Genome-wide genotyping array 2020-05-21 31969693 Coleman JRI 2020-01-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31969693 Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Trauma exposure in major depressive disorder 13,393 European ancestry cases, 9,487 European ancestry controls NA Affymetrix [7791636] (imputed) 19 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST009983 Genome-wide genotyping array 2020-05-21 31969693 Coleman JRI 2020-01-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31969693 Genome-wide gene-environment analyses of major depressive disorder and reported lifetime traumatic experiences in UK Biobank. Trauma exposure in major depressive disorder-negative individuals 10,701 European ancestry cases, 39,677 European ancestry controls NA Affymetrix [7791636] (imputed) 36 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST009984 Genome-wide genotyping array 2022-10-04 32372017 Mosley JD 2020-05-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32372017 The polygenic architecture of left ventricular mass mirrors the clinical epidemiology. Left ventricular mass 7,601 European ancestry individuals NA Illumina [5455089] (imputed) 0 left ventricular mass http://www.ebi.ac.uk/efo/EFO_0009289 GCST012996 Genome-wide genotyping array 2020-08-25 32378780 Park B 2020-05-07 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/32378780 Genome-Wide Association Study of Genetic Variants Related to Anthracycline-Induced Cardiotoxicity in Early Breast Cancer. Anthracycline-induced cardiotoxicity in early breast cancer 42 Korean ancestry cases, 215 Korean ancestry controls NA NR [346946] 7 cardiotoxicity, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_1001482, http://www.ebi.ac.uk/efo/EFO_0005257 GCST010456 Genome-wide genotyping array 2020-08-03 32376702 Shen J 2020-05-06 mSphere www.ncbi.nlm.nih.gov/pubmed/32376702 Genetic Association Reveals Protection against Recurrence of Clostridium difficile Infection with Bezlotoxumab Treatment. Recurrence of Clostridium difficile infection x bezlotuxumab treatment interaction (2df test) 704 European, African American and Asian ancestry individuals NA Affymetrix [7570264] (imputed) 1 clostridium difficile infection, response to bezlotoxumab http://www.ebi.ac.uk/efo/EFO_0009130, http://www.ebi.ac.uk/efo/EFO_0010730 GCST010380 Genome-wide genotyping array 2020-10-27 32363570 Giri AK 2020-05-04 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/32363570 Multifaceted genome-wide study identifies novel regulatory loci in SLC22A11 and ZNF45 for body mass index in Indians. Body mass index 1,142 Indo-European Indian ancestry individuals 6,117 Indo-European Indian ancestry individuals Illumina [537246] 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST010721 Genome-wide genotyping array 2019-06-24 30678657 Westphal S 2019-01-24 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/30678657 Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. Postoperative myocardial infarction after cardiac surgery 87 cases, 939 controls NA Illumina [9007469] (imputed) 2 response to surgery, post-operative myocardial infarction http://www.ebi.ac.uk/efo/EFO_0009951, http://www.ebi.ac.uk/efo/EFO_0009953 GCST007976 Genome-wide genotyping array 2019-06-24 30678657 Westphal S 2019-01-24 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/30678657 Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. Postoperative stroke after cardiac surgery 17 cases, 1,089 controls NA Illumina [9007469] (imputed) 4 post-operative stroke, response to surgery http://www.ebi.ac.uk/efo/EFO_0009956, http://www.ebi.ac.uk/efo/EFO_0009951 GCST007977 Genome-wide genotyping array 2019-06-24 30678657 Westphal S 2019-01-24 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/30678657 Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. Postoperative acute renal failure after cardiac surgery 52 cases, 1,020 controls NA Illumina [9007469] (imputed) 4 post-operative acute kidney injury, response to surgery http://www.ebi.ac.uk/efo/EFO_0009955, http://www.ebi.ac.uk/efo/EFO_0009951 GCST007979 Genome-wide genotyping array 2019-06-24 30678657 Westphal S 2019-01-24 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/30678657 Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. Postoperative atrial fibrillation after cardiac surgery 242 cases, 640 controls NA Illumina [9007469] (imputed) 4 post-operative atrial fibrillation, response to surgery http://www.ebi.ac.uk/efo/EFO_0009952, http://www.ebi.ac.uk/efo/EFO_0009951 GCST007978 Genome-wide genotyping array 2019-06-24 30678657 Westphal S 2019-01-24 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/30678657 Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. Postoperative delirium after cardiac surgery 148 cases, 819 controls NA Illumina [9007469] (imputed) 2 response to surgery, post-operative delirium http://www.ebi.ac.uk/efo/EFO_0009951, http://www.ebi.ac.uk/efo/EFO_0009954 GCST007980 Genome-wide genotyping array 2019-06-24 30678657 Westphal S 2019-01-24 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/30678657 Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study. Postoperative complication after cardiac surgery Up to 1,163 individuals NA Illumina [9007469] (imputed) 3 response to surgery, post-operative sign or symptom http://www.ebi.ac.uk/efo/EFO_0009951, http://www.ebi.ac.uk/efo/EFO_0005323 GCST007981 Genome-wide genotyping array 2019-04-18 30674623 Syreeni A 2019-01-23 Diabetes www.ncbi.nlm.nih.gov/pubmed/30674623 Genetic Determinants of Glycated Hemoglobin in Type 1 Diabetes. Glycated hemoglobin levels in type 1 diabetes 4,622 Finnish ancestry individuals up to 3,097 individuals Illumina [8354674] (imputed) 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST007605 Genome-wide genotyping array 2019-04-18 30661239 Nicoletti P 2019-01-19 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/30661239 Drug-induced injury due to flucloxacillin: relevance of multiple HLA alleles. Drug-induced liver injury (flucloxacillin) 197 European ancestry cases, 6,835 European ancestry controls NA Illumina [NR] (imputed) 11 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST007606 Genome-wide genotyping array 2019-04-18 30661239 Nicoletti P 2019-01-19 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/30661239 Drug-induced injury due to flucloxacillin: relevance of multiple HLA alleles. Drug-induced liver injury (isoxazolyl penicillins) 6 European ancestry cases, 10,588 European ancestry controls NA Illumina [NR] (imputed) 0 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST007608 Genome-wide genotyping array 2019-04-18 30661239 Nicoletti P 2019-01-19 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/30661239 Drug-induced injury due to flucloxacillin: relevance of multiple HLA alleles. Drug-induced liver injury (amoxicillin) 15 European ancestry cases, 10,588 European ancestry controls NA Illumina [NR] (imputed) 0 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST007607 Genome-wide genotyping array 2020-04-20 24326010 Xavier JM 2013-12-10 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/24326010 FUT2: filling the gap between genes and environment in Behçet's disease? Behcet's disease 292 Iranian ancestry cases, 294 Iranian ancestry controls 684 Iranian ancestry cases, 532 Iranian ancestry controls, 1,215 Turkish ancestry cases, 1,278 Turkish ancestry controls Affymetrix [868254] 2 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST009887 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Systolic blood pressure x educational attainment (some college) interaction (2df) 27,617 European ancestry individuals with some college education, 20,253 European ancestry individuals without college education, 8,128 African ancestry individuals with some college education, 8,537 African ancestry individuals without college education, 1,138 Asian ancestry individuals with some college education, 10,214 Asian ancestry individuals without college education, 1,869 Hispanic/Latin American individuals with some college education, 3,276 Hispanic/Latin American individuals without college education 131,584 European ancestry individuals with some college education, 110,940 European ancestry individuals without college education, 1,494 African ancestry individuals with some college education, 5,704 African ancestry individuals without college education, 2,339 Asian ancestry individuals with some college education, 8,567 Asian ancestry individuals without college education, 4,133 Hispanic individuals with some college education, 7,498 Hispanic individuals without college education Affymetrix, Illumina [~ 18800000] (imputed) 7 systolic blood pressure, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010426 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Systolic blood pressure x educational attainment (graduated college) interaction (2df) 27,367 European ancestry college graduated individuals, 51,673 European ancestry non-college graduated individuals, 3,605 African ancestry college graduated individuals, 13,060 African ancestry non-college graduated individuals, 291 Asian ancestry college graduated individuals, 457 Asian ancestry non-college graduated individuals, 786 Hispanic/Latin American college graduated individuals, 4,359 Hispanic/Latin American non-college graduated individuals 67,506 European ancestry college graduated individuals, 189,531 European ancestry non-college graduated individuals, 781 African ancestry college graduated individuals, 6,417 African ancestry non-college graduated individuals, 651 Asian ancestry college graduated individuals, 5,296 Asian ancestry non-college graduated individuals, 1,703 Hispanic college graduated individuals, 9,928 Hispanic non-college graduated individuals Affymetrix, Illumina [~ 18800000] (imputed) 2 systolic blood pressure, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010425 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Diastolic blood pressure x educational attainment (some college) interaction (2df) 27,617 European ancestry individuals with some college education, 20,253 European ancestry individuals without college education, 8,128 African ancestry individuals with some college education, 8,537 African ancestry individuals without college education, 1,138 Asian ancestry individuals with some college education, 10,214 Asian ancestry individuals without college education, 1,869 Hispanic/Latin American individuals with some college education, 3,276 Hispanic/Latin American individuals without college education 131,584 European ancestry individuals with some college education, 110,940 European ancestry individuals without college education, 1,494 African ancestry individuals with some college education, 5,704 African ancestry individuals without college education, 2,339 Asian ancestry individuals with some college education, 8,567 Asian ancestry individuals without college education, 4,133 Hispanic individuals with some college education, 7,498 Hispanic individuals without college education Affymetrix, Illumina [~ 18800000] (imputed) 1 diastolic blood pressure, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010424 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Diastolic blood pressure x educational attainment (graduated college) interaction (2df) 27,367 European ancestry college graduated individuals, 51,673 European ancestry non-college graduated individuals, 3,605 African ancestry college graduated individuals, 13,060 African ancestry non-college graduated individuals, 291 Asian ancestry college graduated individuals, 457 Asian ancestry non-college graduated individuals, 786 Hispanic/Latin American college graduated individuals, 4,359 Hispanic/Latin American non-college graduated individuals 67,506 European ancestry college graduated individuals, 189,531 European ancestry non-college graduated individuals, 781 African ancestry college graduated individuals, 6,417 African ancestry non-college graduated individuals, 651 Asian ancestry college graduated individuals, 5,296 Asian ancestry non-college graduated individuals, 1,703 Hispanic college graduated individuals, 9,928 Hispanic non-college graduated individuals Affymetrix, Illumina [~ 18800000] (imputed) 4 diastolic blood pressure, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010423 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mean arterial pressure x educational attainment (some college) interaction (2df) 27,617 European ancestry individuals with some college education, 20,253 European ancestry individuals without college education, 8,128 African ancestry individuals with some college education, 8,537 African ancestry individuals without college education, 1,138 Asian ancestry individuals with some college education, 10,214 Asian ancestry individuals without college education, 1,869 Hispanic/Latin American individuals with some college education, 3,276 Hispanic/Latin American individuals without college education 131,584 European ancestry individuals with some college education, 110,940 European ancestry individuals without college education, 1,494 African ancestry individuals with some college education, 5,704 African ancestry individuals without college education, 2,339 Asian ancestry individuals with some college education, 8,567 Asian ancestry individuals without college education, 4,133 Hispanic individuals with some college education, 7,498 Hispanic individuals without college education Affymetrix, Illumina [~ 18800000] (imputed) 3 mean arterial pressure, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010422 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Mean arterial pressure x educational attainment (graduated college) interaction (2df) 27,367 European ancestry college graduated individuals, 51,673 European ancestry non-college graduated individuals, 3,605 African ancestry college graduated individuals, 13,060 African ancestry non-college graduated individuals, 291 Asian ancestry college graduated individuals, 457 Asian ancestry non-college graduated individuals, 786 Hispanic/Latin American college graduated individuals, 4,359 Hispanic/Latin American non-college graduated individuals 67,506 European ancestry college graduated individuals, 189,531 European ancestry non-college graduated individuals, 781 African ancestry college graduated individuals, 6,417 African ancestry non-college graduated individuals, 651 Asian ancestry college graduated individuals, 5,296 Asian ancestry non-college graduated individuals, 1,703 Hispanic college graduated individuals, 9,928 Hispanic non-college graduated individuals Affymetrix, Illumina [~ 18800000] (imputed) 2 mean arterial pressure, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010421 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Pulse pressure x educational attainment (some college) interaction (2df) 27,617 European ancestry individuals with some college education, 20,253 European ancestry individuals without college education, 8,128 African ancestry individuals with some college education, 8,537 African ancestry individuals without college education, 1,138 Asian ancestry individuals with some college education, 10,214 Asian ancestry individuals without college education, 1,869 Hispanic/Latin American individuals with some college education, 3,276 Hispanic/Latin American individuals without college education 131,584 European ancestry individuals with some college education, 110,940 European ancestry individuals without college education, 1,494 African ancestry individuals with some college education, 5,704 African ancestry individuals without college education, 2,339 Asian ancestry individuals with some college education, 8,567 Asian ancestry individuals without college education, 4,133 Hispanic individuals with some college education, 7,498 Hispanic individuals without college education Affymetrix, Illumina [~ 18800000] (imputed) 4 pulse pressure measurement, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010420 Genome-wide genotyping array 2020-08-20 32372009 de Las Fuentes L 2020-05-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32372009 Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci. Pulse pressure x educational attainment (graduated college) interaction (2df) 27,367 European ancestry college graduated individuals, 51,673 European ancestry non-college graduated individuals, 3,605 African ancestry college graduated individuals, 13,060 African ancestry non-college graduated individuals, 291 Asian ancestry college graduated individuals, 457 Asian ancestry non-college graduated individuals, 786 Hispanic/Latin American college graduated individuals, 4,359 Hispanic/Latin American non-college graduated individuals 67,506 European ancestry college graduated individuals, 189,531 European ancestry non-college graduated individuals, 781 African ancestry college graduated individuals, 6,417 African ancestry non-college graduated individuals, 651 Asian ancestry college graduated individuals, 5,296 Asian ancestry non-college graduated individuals, 1,703 Hispanic college graduated individuals, 9,928 Hispanic non-college graduated individuals Affymetrix, Illumina [~ 18800000] (imputed) 0 pulse pressure measurement, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0004784 GCST010419 Genome-wide genotyping array 2021-05-27 33109212 Chang H 2020-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/33109212 Genetic architecture of cardiometabolic risks in people living with HIV. Triglyceride levels in HIV infection 3,095 European ancestry individuals, 3,189 African American individuals NA Illumina [13620258] (imputed) 70 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011742 Genome-wide genotyping array 2021-05-27 33109212 Chang H 2020-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/33109212 Genetic architecture of cardiometabolic risks in people living with HIV. LDL cholesterol levels in HIV infection 3,095 European ancestry individuals, 3,189 African American individuals NA Illumina [13620258] (imputed) 76 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST011741 Genome-wide genotyping array 2021-05-27 33109212 Chang H 2020-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/33109212 Genetic architecture of cardiometabolic risks in people living with HIV. HDL cholesterol levels in HIV infection 3,095 European ancestry individuals, 3,189 African American individuals NA Illumina [13620258] (imputed) 86 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST011743 Genome-wide genotyping array 2016-09-12 26379185 Garcia-Etxebarria K 2015-09-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/26379185 No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. Influenza A (H1N1) severity 49 European ancestry severe cases, 107 European ancestry mild cases NA Affymetrix [547296] 7 influenza A severity measurement http://www.ebi.ac.uk/efo/EFO_0007743 GCST003126 Genome-wide genotyping array 2016-09-12 26379185 Garcia-Etxebarria K 2015-09-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/26379185 No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. Influenza A (H1N1) infection 49 European ancestry severe cases, 107 European ancestry mild cases, 549 European ancestry population controls NA Affymetrix [547296] 14 influenza A (H1N1) http://www.ebi.ac.uk/efo/EFO_1001488 GCST003125 Genome-wide genotyping array 2016-09-12 26379185 Garcia-Etxebarria K 2015-09-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/26379185 No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. Mild influenza (H1N1) infection 107 European ancestry mild cases, 549 European ancestry population controls NA Affymetrix [547296] 35 influenza A (H1N1) http://www.ebi.ac.uk/efo/EFO_1001488 GCST003124 Genome-wide genotyping array 2016-09-12 26379185 Garcia-Etxebarria K 2015-09-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/26379185 No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity. Severe influenza A (H1N1) infection 49 European ancestry severe cases, 549 European ancestry population controls NA Affymetrix [547296] 34 influenza A (H1N1) http://www.ebi.ac.uk/efo/EFO_1001488 GCST003123 Genome-wide genotyping array 2016-09-12 26325155 Brehm JM 2015-09-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26325155 A Genome-Wide Association Study of Post-bronchodilator Lung Function in Children with Asthma. Post-bronchodilator lung function in asthma (FEV1) 447 Puerto Rican ancestry cases 568 European, black or Hispanic cases, 2,414 Hispanic cases Illumina [NR] 0 pulmonary function measurement, forced expiratory volume, response to bronchodilator http://www.ebi.ac.uk/efo/EFO_0003892, http://www.ebi.ac.uk/efo/EFO_0004314, http://purl.obolibrary.org/obo/GO_0097366 GCST003110 Genome-wide genotyping array 2016-09-12 26325155 Brehm JM 2015-09-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26325155 A Genome-Wide Association Study of Post-bronchodilator Lung Function in Children with Asthma. Post-bronchodilator lung function in asthma (FEV1/FVC) 447 Puerto Rican ancestry cases 568 European, black or Hispanic cases, 2,414 Hispanic cases Illumina [NR] 0 pulmonary function measurement, response to bronchodilator, FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0003892, http://purl.obolibrary.org/obo/GO_0097366, http://www.ebi.ac.uk/efo/EFO_0004713 GCST003107 Genome-wide genotyping array 2016-04-12 26385043 Kertai MD 2015-06-17 Am Heart J www.ncbi.nlm.nih.gov/pubmed/26385043 Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery. Postoperative atrial fibrillation in coronary artery bypass grafting surgery 620 European ancestry cases, 257 European ancestry controls 220 cases, 84 controls Illumina [524975] 3 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST002975 Genome-wide genotyping array 2016-09-21 26366535 Sood RF 2015-10-01 Ann Surg www.ncbi.nlm.nih.gov/pubmed/26366535 Genome-wide Association Study of Postburn Scarring Identifies a Novel Protective Variant. Postburn hypertrophic scarring severity 408 European ancestry individuals, 26 Asian ancestry individuals, 19 African American individuals, 11 Native American ancestry individuals, 74 individuals NA Illumina [289639] 1 postburn hypertrophic scarring severity measurement http://www.ebi.ac.uk/efo/EFO_0007747 GCST003146 Genome-wide genotyping array 2016-09-07 26416764 Day FR 2015-09-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26416764 Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome. Polycystic ovary syndrome 5,184 European ancestry cases, 82,759 European ancestry controls 374 European ancestry cases, 92,681 European ancestry controls, 1,671 cases, 6,205 controls Illumina [~ 9000000] (imputed) 9 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST003144 Genome-wide genotyping array 2016-09-19 26451028 Hofer E 2015-10-08 Stroke www.ncbi.nlm.nih.gov/pubmed/26451028 White Matter Lesion Progression: Genome-Wide Search for Genetic Influences. White matter lesion progression 1,085 European ancestry elderly cases, 6,688 European ancestry elderly controls NA Affymetrix, Illumina [up to 2543887] (imputed) 7 white matter lesion progression measurement http://www.ebi.ac.uk/efo/EFO_0007746 GCST003151 Genome-wide genotyping array 2016-09-19 26451028 Hofer E 2015-10-08 Stroke www.ncbi.nlm.nih.gov/pubmed/26451028 White Matter Lesion Progression: Genome-Wide Search for Genetic Influences. White matter lesion progression (adjusted for white matter lesion burden at baseline) 1,085 European ancestry elderly cases, 6,688 European ancestry elderly controls NA Affymetrix, Illumina [up to 2543887] (imputed) 6 white matter lesion progression measurement http://www.ebi.ac.uk/efo/EFO_0007746 GCST003152 Genome-wide genotyping array 2016-09-07 26352407 Raffler J 2015-09-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26352407 Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality. Urinary metabolites 3,861 European ancestry individuals 1,691European ancestry individuals Affymetrix [620456] 20 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST003119 Genome-wide genotyping array 2016-09-07 26416757 Band G 2015-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/26416757 A novel locus of resistance to severe malaria in a region of ancient balancing selection. Severe malaria 5,130 African ancestry cases, 5,291 African ancestry controls 5,535 African ancestry cases, 9,948 African ancestry controls Illumina [~ 38000000] (imputed) 3 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST003145 Genome-wide genotyping array 2016-10-04 26440539 Hancock DB 2015-10-06 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/26440539 Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence. Nicotine dependence 9,137 European ancestry mild cases, 4,881 European ancestry moderate cases, 3,056 European ancestry severe cases 2,662 European ancestry mild cases, 3,044 European ancestry moderate cases, 1,763 European ancestry severe cases Illumina [8548225] (imputed) 3 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST003185 Genome-wide genotyping array 2016-09-19 26450422 DeLorenze GN 2015-10-08 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/26450422 Polymorphisms in HLA Class II Genes Are Associated With Susceptibility to Staphylococcus aureus Infection in a White Population. Staphylococcus aureus infection 4,701 European ancestry cases, 45,344 European ancestry controls NA Affymetrix [at least 584535] (imputed) 2 Staphylococcus aureus infection http://www.ebi.ac.uk/efo/EFO_0005681 GCST003150 Genome-wide genotyping array 2016-09-19 26450422 DeLorenze GN 2015-10-08 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/26450422 Polymorphisms in HLA Class II Genes Are Associated With Susceptibility to Staphylococcus aureus Infection in a White Population. Skin and soft tissue Staphylococcus aureus infection 2,130 European ancestry cases, 45,434 European ancestry controls NA Affymetrix [at least 584535] (imputed) 1 skin and soft tissue Staphylococcus aureus infection http://www.ebi.ac.uk/efo/EFO_1001489 GCST003149 Genome-wide genotyping array 2016-07-08 26089329 Carty CL 2015-06-18 Stroke www.ncbi.nlm.nih.gov/pubmed/26089329 Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans. Ischemic stroke up to 1,365 African American cases, up to 13,154 African American controls European ancestry individuals (see Traylor, 2012) Affymetrix, Illumina [~ 2600000] (imputed) 9 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST002988 Genome-wide genotyping array 2016-07-08 26089329 Carty CL 2015-06-18 Stroke www.ncbi.nlm.nih.gov/pubmed/26089329 Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans. Stroke up to 1,592 African American cases, up to 13,154 African American controls NA Affymetrix, Illumina [up to 2600000] (imputed) 27 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST002987 Genome-wide genotyping array 2016-05-17 26075790 Kelemen LE 2015-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26075790 Genome-wide significant risk associations for mucinous ovarian carcinoma. Mucinous ovarian carcinoma 1,003 European ancestry invasive cases, 641 European ancestry low malignant potential cases, 21,693 European ancestry controls NA Illumina [15504273] (imputed) 6 ovarian mucinous adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0006462 GCST002967 Genome-wide genotyping array 2016-06-29 26199339 Liu CY 2015-07-21 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/26199339 Genome-wide Gene-Asbestos Exposure Interaction Association Study Identifies a Common Susceptibility Variant on 22q13.31 Associated with Lung Cancer Risk. Lung cancer (asbestos exposure interaction) 833 European ancestry cases, 739 European ancestry controls 2,960 European ancestry cases, 2,646 European ancestry controls Illumina [4649540] 0 lung carcinoma, asbestos exposure measurement http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0004806 GCST003049 Genome-wide genotyping array 2016-04-28 26154020 Ferrari R 2015-06-12 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/26154020 A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia. Frontotemporal dementia 530 European ancestry cases, 926 European ancestry controls NA Illumina [2292247] (imputed) 9 frontotemporal dementia http://purl.obolibrary.org/obo/MONDO_0017276 GCST002960 Genome-wide genotyping array 2016-07-11 26121033 Grondin Y 2015-06-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/26121033 Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise. Hearing loss in noise exposure 19 European and Mexican ancestry cases, 22 European and Mexican ancestry controls NA Affymetrix [289036] 1 noise-induced hearing loss http://www.ebi.ac.uk/efo/EFO_1001254 GCST003006 Genome-wide genotyping array 2016-11-18 26815016 Julia A 2016-01-27 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/26815016 Identification of IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis in a Genome-Wide Association Study. Rheumatoid factor seropositivity in rheumatoid arthritis 896 Spanish ancestry rheumatoid factor-positive cases, 282 Spanish ancestry rheumatoid factor-negative cases 472 Spanish ancestry rheumatoid factor-positive cases, 190 Spanish ancestry rheumatoid factor-negative cases Illumina [509374] 1 rheumatoid factor seropositivity measurement, rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0007791, http://www.ebi.ac.uk/efo/EFO_0005767 GCST003330 Genome-wide genotyping array 2016-10-12 26586795 Phipps AI 2015-11-19 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/26586795 Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis. Survival in colorectal cancer up to 2,843 European ancestry cases without distant metastases, up to 462 European ancestry cases with distant metastases, up to 189 European ancestry cases of unknown stage up to 3,205 European ancestry cases without distant metastases, up to 435 European ancestry cases with distant metastases, up to 124 European ancestry cases of unknown stage Illumina [~ 2700000] (imputed) 1 survival time, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0005575 GCST003229 Genome-wide genotyping array 2016-10-12 26586795 Phipps AI 2015-11-19 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/26586795 Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis. Survival in colorectal cancer (non-distant metastatic) up to 2,843 European ancestry cases up to 3,205 European ancestry cases Illumina [~ 2700000] (imputed) 1 metastasis measurement, survival time, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0007675, http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0005575 GCST003231 Genome-wide genotyping array 2016-10-12 26586795 Phipps AI 2015-11-19 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/26586795 Common genetic variation and survival after colorectal cancer diagnosis: a genome-wide analysis. Survival in colorectal cancer (distant metastatic) up to 462 European ancestry cases up to 435 European ancestry cases Illumina [~ 2700000] (imputed) 4 metastasis measurement, survival time, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0007675, http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0005575 GCST003230 Genome-wide genotyping array 2016-06-10 26151821 Schumacher FR 2015-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26151821 Genome-wide association study of colorectal cancer identifies six new susceptibility loci. Colorectal cancer 18,299 European ancestry cases, 19,656 European ancestry controls 4,725 East Asian ancestry cases, 9,969 East Asian ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 22 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST003017 Genome-wide genotyping array 2016-11-10 26811534 Wang X 2016-01-25 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/26811534 CELF4 Variant and Anthracycline-Related Cardiomyopathy: A Children's Oncology Group Genome-Wide Association Study. Cardiomyopathy in childhood cancer survivors (anthracycline treatment interaction) 112 European ancestry cases, 219 European ancestry controls 21 European ancestry cases, 12 Hispanic cases, 21 cases Illumina [583748] 0 response to anthracycline-based chemotherapy, cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0005257, http://www.ebi.ac.uk/efo/EFO_0000318 GCST003300 Genome-wide genotyping array 2016-11-10 26811534 Wang X 2016-01-25 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/26811534 CELF4 Variant and Anthracycline-Related Cardiomyopathy: A Children's Oncology Group Genome-Wide Association Study. Cardiomyopathy in childhood cancer survivors 112 European ancestry cases, 219 European ancestry controls 21 European ancestry cases, 12 Hispanic cases, 21 cases Illumina [583748] 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST003299 Genome-wide genotyping array 2015-12-03 25774636 Curtis J 2015-03-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25774636 Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration. Tuberculosis 5,530 European ancestry cases, 5,607 European ancestry controls 1,085 Russian ancestry cases, 2,865 Russian ancestry controls, 2,277 Sub-Saharan African ancestry cases, 2,360 Sub-Saharan African ancestry controls Affymetrix [7614862] (imputed) 2 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST002810 Genome-wide genotyping array 2016-10-05 26531332 Kim LH 2015-11-14 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26531332 Genome-wide association study with the risk of schizophrenia in a Korean population. Schizophrenia 350 Korean ancestry cases, 700 Korean ancestry controls 310 Korean ancestry cases, 604 Korean ancestry controls Illumina [620001] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST003190 Genome-wide genotyping array 2017-06-13 28232668 Yu Y 2017-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28232668 Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity. Nonsyndromic cleft lip with cleft palate 2,033 Han Chinese ancestry cases, 4,051 Han Chinese ancestry controls 1,346 Han Chinese ancestry cases, 4,542 Han Chinese ancestry controls Illumina [803202] 56 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST004166 Genome-wide genotyping array 2017-02-22 27304844 Khong JJ 2016-06-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/27304844 Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy. Thyroid-associated orbitopathy in graves' disease 265 European ancestry cases with thyroid-associated orbitopathy, 147 European ancestry cases without thyroid-associated orbitopathy 319 European ancestry cases with thyroid-associated orbitopathy, 220 European ancestry cases without thyroid-associated orbitopathy Illumina [2200000] 1 Graves ophthalmopathy http://www.ebi.ac.uk/efo/EFO_1001466 GCST003640 Genome-wide genotyping array 2017-02-22 27347659 Vaysse A 2016-06-27 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/27347659 A comprehensive genome-wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variants. Breslow thickness in cutaneous melanoma 966 European ancestry individuals 1,546 European ancestry individuals Illumina [up to 1067258] (imputed) 0 Breslow thickness http://www.ebi.ac.uk/efo/EFO_0004955 GCST003639 Genome-wide genotyping array 2017-03-17 27089181 Okbay A 2016-04-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27089181 Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Subjective well-being 298,420 Korculan (founder/genetic isolate), Split (founder/genetic isolate), Vis (founder/genetic isolate), Erasmus Rucphen (founder/genetic isolate) and other European ancestry individuals NA Affymetrix, Illumina, Perlegen [at least 5170349] (imputed) 113 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST003766 Genome-wide genotyping array 2017-03-17 27089181 Okbay A 2016-04-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27089181 Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Life satisfaction 166,205 European ancestry individuals NA Affymetrix, Illumina, Perlegen [at least 5170349] (imputed) 28 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST003767 Genome-wide genotyping array 2017-03-17 27089181 Okbay A 2016-04-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27089181 Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Positive affect 180,281 Korculan (founder/genetic isolate), Split (founder/genetic isolate), Vis (founder/genetic isolate), Erasmus Rucphen (founder/genetic isolate) and other European ancestry individuals NA Affymetrix, Illumina, Perlegen [at least 5170349] (imputed) 30 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST003768 Genome-wide genotyping array 2017-03-17 27089181 Okbay A 2016-04-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27089181 Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Depression 105,739 European ancestry individuals, 16,471 European ancestry major depressive disorder cases, 58,835 European ancestry controls 368,890 European ancestry individuals Affymetrix [up to 6544862] (imputed) 15 unipolar depression, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007006 GCST003769 Genome-wide genotyping array 2017-03-17 27089181 Okbay A 2016-04-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27089181 Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Neuroticism 170,911 European ancestry individuals NA Affymetrix [up to 6544775] (imputed) 114 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST003770 Genome-wide genotyping array 2017-02-19 27399966 Morris DL 2016-07-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27399966 Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. Systemic lupus erythematosus 1,659 Chinese ancestry cases, 3,398 Chinese ancestry controls, 4,036 European ancestry cases, 6,959 European ancestry controls 3,043 Chinese ancestry cases, 5,074 Chinese ancestry controls, 2,643 European ancestry cases, 9,032 European ancestry controls NR [6344733] (imputed) 74 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST003622 Genome-wide genotyping array 2019-08-23 25920553 Coleman C 2015-04-29 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25920553 Common polygenic variation in coeliac disease and confirmation of ZNF335 and NIFA as disease susceptibility loci. Celiac disease 425 Irish ancestry cases, 453 Irish ancestry controls 11,812 European ancestry cases, 229 Indian ancestry cases, 11,837 European ancestry controls, 391 Indian ancestry controls Illumina [up to 143074] 23 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST008489 Targeted genotyping array [Immunochip] 2017-03-20 27393504 Zanetti KA 2016-05-13 Lung Cancer www.ncbi.nlm.nih.gov/pubmed/27393504 Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Lung cancer 1,737 African American cases, 3,602 African American controls 866 African American cases, 796 African American controls Illumina [1024001] 6 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST003775 Genome-wide genotyping array 2017-03-20 27393504 Zanetti KA 2016-05-13 Lung Cancer www.ncbi.nlm.nih.gov/pubmed/27393504 Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Smoking status (current vs former) 2029 African American current smoker individuals, 1748 African American former smoker individuals NA Illumina [1024001] 1 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST003778 Genome-wide genotyping array 2017-03-20 27393504 Zanetti KA 2016-05-13 Lung Cancer www.ncbi.nlm.nih.gov/pubmed/27393504 Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Smoking behaviour (cigarettes smoked per day) up to 4737 African American individuals NA Illumina [1024001] 1 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST003779 Genome-wide genotyping array 2017-03-20 27393504 Zanetti KA 2016-05-13 Lung Cancer www.ncbi.nlm.nih.gov/pubmed/27393504 Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Lung adenocarcinoma 739 African American cases, 3,601 African American controls up to 311 African American cases, up to 1,137 African American controls Illumina [1024001] 1 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST003776 Genome-wide genotyping array 2017-03-20 27393504 Zanetti KA 2016-05-13 Lung Cancer www.ncbi.nlm.nih.gov/pubmed/27393504 Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population. Squamous cell lung carcinoma up to 400 African American cases, up to 3,601 African American controls up to 192 African American cases, up to 1,137 African American controls Illumina [1024001] 0 squamous cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000708 GCST003777 Genome-wide genotyping array 2016-12-01 27016271 Kornilov SA 2016-03-25 Pediatrics www.ncbi.nlm.nih.gov/pubmed/27016271 Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population. Developmental language disorder 149 isolated population cases, 210 isolated population controls NA Illumina [223580] 4 specific language impairment http://www.ebi.ac.uk/efo/EFO_1001510 GCST003396 Genome-wide genotyping array 2016-12-01 27016271 Kornilov SA 2016-03-25 Pediatrics www.ncbi.nlm.nih.gov/pubmed/27016271 Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population. Developmental language disorder (linguistic errors) 149 isolated population cases, 210 isolated population controls NA Illumina [223580] 9 linguistic error measurement, specific language impairment http://www.ebi.ac.uk/efo/EFO_0007798, http://www.ebi.ac.uk/efo/EFO_1001510 GCST003397 Genome-wide genotyping array 2016-12-01 27016271 Kornilov SA 2016-03-25 Pediatrics www.ncbi.nlm.nih.gov/pubmed/27016271 Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population. Developmental language disorder (syntactic complexity) 149 isolated population cases, 210 isolated population controls NA Illumina [223580] 3 syntactic complexity measurement, specific language impairment http://www.ebi.ac.uk/efo/EFO_0007799, http://www.ebi.ac.uk/efo/EFO_1001510 GCST003398 Genome-wide genotyping array 2016-12-11 27047539 Fridley BL 2016-03-22 Front Genet www.ncbi.nlm.nih.gov/pubmed/27047539 Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence. Response to carboplatin in ovarian cancer (MTT IC50) 74 lymphoblastoid cell lines NA Illumina [6243550] (imputed) 2 response to platinum based chemotherapy, cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0006952 GCST003440 Genome-wide genotyping array 2016-12-11 27047539 Fridley BL 2016-03-22 Front Genet www.ncbi.nlm.nih.gov/pubmed/27047539 Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence. Response to carboplatin and paclitaxel in ovarian cancer (Caspase 3/7 EC50) 74 lymphoblastoid cell lines NA Illumina [6243550] (imputed) 3 response to platinum based chemotherapy, methylcobalamin deficiency type cblE, cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0004647, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0006952 GCST003443 Genome-wide genotyping array 2016-12-11 27047539 Fridley BL 2016-03-22 Front Genet www.ncbi.nlm.nih.gov/pubmed/27047539 Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence. Response to paclitaxel in ovarian cancer (Caspase 3/7 EC50) 74 lymphoblastoid cell lines NA Illumina [6243550] (imputed) 2 response to platinum based chemotherapy, cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0006952 GCST003439 Genome-wide genotyping array 2016-12-11 27047539 Fridley BL 2016-03-22 Front Genet www.ncbi.nlm.nih.gov/pubmed/27047539 Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence. Response to carboplatin in ovarian cancer (Caspase 3/7 EC50) 74 lymphoblastoid cell lines NA Illumina [6243550] (imputed) 0 response to platinum based chemotherapy, cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0006952 GCST003442 Genome-wide genotyping array 2016-12-11 27047539 Fridley BL 2016-03-22 Front Genet www.ncbi.nlm.nih.gov/pubmed/27047539 Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence. Response to paclitaxel in ovarian cancer (MTT IC50) 74 lymphoblastoid cell lines NA Illumina [6243550] (imputed) 1 methylcobalamin deficiency type cblE, cytotoxicity measurement http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0006952 GCST003441 Genome-wide genotyping array 2016-12-11 27047539 Fridley BL 2016-03-22 Front Genet www.ncbi.nlm.nih.gov/pubmed/27047539 Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence. Response to carboplatin and paclitaxel in ovarian cancer (MTT IC50) 74 lymphoblastoid cell lines NA Illumina [6243550] (imputed) 2 response to platinum based chemotherapy, methylcobalamin deficiency type cblE, cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0004647, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0006952 GCST003444 Genome-wide genotyping array 2016-07-23 26198764 Goes FS 2015-07-21 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26198764 Genome-wide association study of schizophrenia in Ashkenazi Jews. Schizophrenia 1,505 Ashkenazi Jewish founder cases, 2,553 Ashkenazi Jewish founder controls NA Illumina [up to 9792010] (imputed) 29 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST003050 Genome-wide genotyping array 2016-07-23 26198764 Goes FS 2015-07-21 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26198764 Genome-wide association study of schizophrenia in Ashkenazi Jews. Schizophrenia 592 Ashkenazi Jewish ancestry cases, 505 Ashkenazi Jewish ancestry controls, 36,989 cases, 113,075 controls NA Illumina [7158791] (imputed) 620 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST003048 Genome-wide genotyping array 2016-08-16 26305897 Iyengar SK 2015-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26305897 Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND). Diabetic kidney disease 1,564 African American cases, 369 African American diabetic controls, 1,288 African American non-diabetic controls, 538 American Indian ancestry cases, 319 American Indian ancestry diabetic controls, 342 European ancestry cases, 404 European ancestry diabetic controls, 779 Mexican ancestry cases, 594 Mexican ancestry diabetic controls 950 African American cases, 50 African American diabetic controls, 1,887 African American non-diabetic controls, 471 American Indian ancestry cases, 340 American Indian ancestry diabetic controls, 486 American Indian ancestry non-diabetic controls, 582 European ancestry ancestry cases, 205 European ancestry diabetic controls, 2,568 European ancestry non-diabetic controls Affymetrix [NR] 38 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST003098 Genome-wide genotyping array 2016-08-16 26305897 Iyengar SK 2015-08-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26305897 Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND). Diabetic kidney disease up to 1,564 African American cases, 369 African American diabetic controls, 1,288 African American non-diabetic controls, 538 American Indian ancestry cases, 319 American Indian ancestry diabetic controls, 342 European ancestry cases, 404 European ancestry diabetic controls, 779 Mexican ancestry cases, 594 Mexican ancestry diabetic controls NA Affymetrix [NR] 20 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST003099 Genome-wide genotyping array 2016-07-15 26316170 Demirci FY 2015-08-28 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/26316170 Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry. Systemic lupus erythematosus 661 European ancestry cases, 487 European ancestry controls 4,467 European ancestry cases, 9,114 European ancestry controls Affymetrix [up to 700598] 7 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST003103 Genome-wide genotyping array 2016-06-17 26301497 Dina C 2015-08-24 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26301497 Genetic association analyses highlight biological pathways underlying mitral valve prolapse. Mitral valve prolapse 1,442 European ancestry cases, 2,439 European ancestry controls 1,422 European ancestry cases, 6,779 European ancestry controls Affymetrix, Illumina [~ 4800000] (imputed) 8 Mitral valve prolapse http://purl.obolibrary.org/obo/HP_0001634 GCST003094 Genome-wide genotyping array 2016-06-21 26098869 Childs EJ 2015-06-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26098869 Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer. Pancreatic cancer 7,638 cases, 7,364 controls 2,287 cases, 4,205 controls Illumina [866891] (imputed) 17 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST002991 Genome-wide genotyping array 2016-07-11 26084801 Mirabello L 2015-06-17 Cancer Discov www.ncbi.nlm.nih.gov/pubmed/26084801 A Genome-Wide Scan Identifies Variants in NFIB Associated with Metastasis in Patients with Osteosarcoma. Metastasis at diagnosis in osteosarcoma 122 European ancestry cases with metastasis, 419 European ancestry cases without metastasis 43 European ancestry cases with metastasis, 22 African ancestry cases with metastasis, 40 Brazilian ancestry cases with metastasis, 183 European ancestry cases without metastasis, 39 African ancestry cases without metastasis, 67 Brazilian ancestry cases without metastasis Illumina [447040] 2 metastasis measurement, date of diagnosis http://www.ebi.ac.uk/efo/EFO_0007675, http://www.ebi.ac.uk/efo/EFO_0004953 GCST002978 Genome-wide genotyping array 2016-10-05 26434682 Lin YJ 2015-11-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26434682 Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan. Coronary artery aneurysm in Kawasaki disease 76 Han Chinese ancestry child cases, 186 Han Chinese ancestry child controls NA Affymetrix [906600] 2 coronary aneurysm http://www.ebi.ac.uk/efo/EFO_1000881 GCST003192 Genome-wide genotyping array 2016-09-12 26421299 Li J 2015-09-03 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/26421299 Genetic Interactions Explain Variance in Cingulate Amyloid Burden: An AV-45 PET Genome-Wide Association and Interaction Study in the ADNI Cohort. Cingulate cortical amyloid beta load 215 European ancestry early mild cognitive impairment cases, 152 European ancestry late mild cognitive impairment cases, 45 European ancestry Alzheimer disease cases, 190 European ancestry controls NA Illumina [582718] 5 amyloid-beta measurement, cingulate cortex measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0007738 GCST003113 Genome-wide genotyping array 2016-10-06 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Cardiovascular disease in hypertension (calcium channel blocker interaction) Up to 3,527 European ancestry individuals with cardiovascular disease, up to 11,848 European ancestry individuals without cardiovascular disease Up to 1,751 European ancestry individuals with cardiovascular disease, up to 1,267 African American ancestry individuals with cardiovascular disease, up to 2,874 African American ancestry individuals without cardiovascular disease Affymetrix, Illumina [1807456] (imputed) 2 cardiovascular disease, response to calcium channel blocker http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0007767 GCST003205 Genome-wide genotyping array 2016-10-06 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Myocardial infarction in hypertension (calcium channel blocker interaction) Up to 2,114 European ancestry individuals with myocardial infarction, up to 13,261 European ancestry individuals without myocardial infarction Up to 1,171 European ancestry individuals with myocardial infarction Affymetrix, Illumina [1194322] (imputed) 1 response to calcium channel blocker, myocardial infarction http://www.ebi.ac.uk/efo/EFO_0007767, http://www.ebi.ac.uk/efo/EFO_0000612 GCST003206 Genome-wide genotyping array 2016-10-06 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Cardiovascular disease in hypertension (diuretic interaction) Up to 3,527 European ancestry individuals with cardiovascular disease, up to 11,848 European ancestry individuals without cardiovascular disease Up to 1,751 European ancestry individuals with cardiovascular disease, up to 1,267 African American ancestry individuals with cardiovascular disease, up to 2,874 African American ancestry individuals without cardiovascular disease Affymetrix, Illumina [2030893] (imputed) 0 response to diuretic, cardiovascular disease http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0000319 GCST003204 Genome-wide genotyping array 2016-10-06 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Cardiovascular disease in hypertension (beta blocker interaction) Up to 3,527 European ancestry individuals with cardiovascular disease, up to 11,848 European ancestry individuals without cardiovascular disease Up to 1,751 European ancestry individuals with cardiovascular disease, up to 1,267 African American ancestry individuals with cardiovascular disease, up to 2,874 African American ancestry individuals without cardiovascular disease Affymetrix, Illumina [1971049] (imputed) 0 response to beta blocker, cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0000319 GCST003203 Genome-wide genotyping array 2016-10-04 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Myocardial infarction in hypertension (ACE inhibitor interaction) Up to 2,114 European ancestry individuals with myocardial infarction, up to 13,261 European ancestry individuals without myocardial infarction Up to 1,171 European ancestry individuals with myocardial infarction Affymetrix, Illumina [1465692] (imputed) 0 response to angiotensin-converting enzyme inhibitor, myocardial infarction http://www.ebi.ac.uk/efo/EFO_0005325, http://www.ebi.ac.uk/efo/EFO_0000612 GCST003187 Genome-wide genotyping array 2016-10-06 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Myocardial infarction in hypertension (beta blocker interaction) Up to 2,114 European ancestry individuals with myocardial infarction, up to 13,261 European ancestry individuals without myocardial infarction Up to 1,171 European ancestry individuals with myocardial infarction Affymetrix, Illumina [1780479] (imputed) 0 response to beta blocker, myocardial infarction http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0000612 GCST003201 Genome-wide genotyping array 2016-10-06 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Myocardial infarction in hypertension (diuretic interaction) Up to 2,114 European ancestry individuals with myocardial infarction, up to 13,261 European ancestry individuals myocardial infarction Up to 1,171 European ancestry individuals with myocardial infarction Affymetrix, Illumina [1822485] (imputed) 0 response to diuretic, myocardial infarction http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0000612 GCST003202 Genome-wide genotyping array 2016-10-04 26516778 Bis JC 2015-10-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/26516778 Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium. Cardiovascular disease in hypertension (ACE inhibitor interaction) Up to 3,527 European ancestry individuals with cardiovascular disease, up to 11,848 European ancestry individuals without cardiovascular disease Up to 1,751 European ancestry individuals with cardiovascular disease, up to 1,267 African American ancestry individuals with cardiovascular disease, up to 2,874 African American ancestry individuals without cardiovascular disease Affymetrix, Illumina [1892626] (imputed) 1 cardiovascular disease, response to angiotensin-converting enzyme inhibitor http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0005325 GCST003186 Genome-wide genotyping array 2016-07-20 26219847 Adams HH 2015-07-28 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/26219847 Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants. Gait variability 2,946 individuals NA Illumina [6200000] (imputed) 3 gait measurement http://www.ebi.ac.uk/efo/EFO_0007680 GCST003056 Genome-wide genotyping array 2016-07-20 26219847 Adams HH 2015-07-28 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/26219847 Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants. Gait rhythm 2,946 individuals NA Illumina [6200000] (imputed) 5 gait measurement http://www.ebi.ac.uk/efo/EFO_0007680 GCST003054 Genome-wide genotyping array 2016-07-20 26219847 Adams HH 2015-07-28 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/26219847 Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants. Tandem gait 2,946 individuals NA Illumina [6200000] (imputed) 5 gait measurement http://www.ebi.ac.uk/efo/EFO_0007680 GCST003055 Genome-wide genotyping array 2016-04-23 26073756 McGeachie MJ 2015-06-12 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/26073756 CTNNA3 and SEMA3D: Promising loci for asthma exacerbation identified through multiple genome-wide association studies. Asthma exacerbations 581 European ancestry cases 652 European ancestry cases, 212 African American cases, 127 cases Illumina [> 6500000] (imputed) 0 asthma exacerbation measurement http://www.ebi.ac.uk/efo/EFO_0007614 GCST002962 Genome-wide genotyping array 2016-11-29 26806518 Hou L 2016-01-22 Lancet www.ncbi.nlm.nih.gov/pubmed/26806518 Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. Response to lithium treatment in bipolar disorder (dichotomous phenotype) 659 European ancestry responders, 44 East Asian ancestry responders, 1,684 European ancestry non-responders, 176 East Asian ancestry non-responders NA Affymetrix, Illumina [> 6000000] (imputed) 1 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST003378 Genome-wide genotyping array 2021-10-15 26806518 Hou L 2016-01-22 Lancet www.ncbi.nlm.nih.gov/pubmed/26806518 Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. Response to lithium treatment in bipolar disorder (continuous phenotype) 2,039 European ancestry individuals NA Affymetrix, Illumina [> 6000000] (imputed) 4 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST012487 Genome-wide genotyping array 2021-10-15 26806518 Hou L 2016-01-22 Lancet www.ncbi.nlm.nih.gov/pubmed/26806518 Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. Response to lithium treatment in bipolar disorder (dichotomous phenotype) 659 European ancestry responders, 1,684 European ancestry non-responders NA Affymetrix, Illumina [> 6000000] (imputed) 3 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST012486 Genome-wide genotyping array 2021-05-27 26806518 Hou L 2016-01-22 Lancet www.ncbi.nlm.nih.gov/pubmed/26806518 Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. Response to lithium treatment in bipolar disorder (continuous phenotype) 2,039 European ancestry individuals, 194 East Asian ancestry individuals NA Affymetrix, Illumina [> 6000000] (imputed) 2 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST011750 Genome-wide genotyping array 2016-07-13 26121980 Chauhan L 2015-06-30 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/26121980 Genome-wide association analysis identified splicing single nucleotide polymorphism in CFLAR predictive of triptolide chemo-sensitivity. Triptolide cytotoxicity 55 European ancestry lymphoblastoid cell lines NA Affymetrix, Illumina, Perlegen [at least 1978803] (imputed) 16 response to triptolide, cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0007662, http://www.ebi.ac.uk/efo/EFO_0006952 GCST003008 Genome-wide genotyping array 2016-04-23 26100964 Cao S 2015-06-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26100964 Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients. Platinum-induced hepatotoxicity in non-small cell lung cancer 329 Han Chinese ancestry cases 375 Han Chinese ancestry cases Affymetrix [588732] 0 response to platinum based chemotherapy, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0004228 GCST002993 Genome-wide genotyping array 2016-06-08 26083242 Dahlin A 2015-06-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/26083242 Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma. Response to montelukast in asthma (change in FEV1) 88 European ancestry cases, 10 African ancestry cases, 35 Asian ancestry cases 101 European ancestry cases, 33 African ancestry cases, 50 Asian ancestry cases Illumina [532264] 2 FEV change measurement, response to montelukast http://www.ebi.ac.uk/efo/EFO_0005921, http://www.ebi.ac.uk/efo/EFO_0007612 GCST002979 Genome-wide genotyping array 2016-08-22 26307654 Szulkin R 2015-08-25 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/26307654 Genome-wide association study of prostate cancer-specific survival. Prostate cancer (survival) 7,322 cases 18,197 European ancestry cases Affymetrix, Illumina [up to 9536409] (imputed) 4 survival time, prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0001663 GCST003100 Genome-wide genotyping array 2016-09-27 26620591 Barreto-Luis A 2015-11-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/26620591 Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene. Asthma 352 European ancestry cases, 537 European ancestry controls 828 European ancestry cases, 1,378 European ancestry controls Affymetrix [6467565] (imputed) 2 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003176 Genome-wide genotyping array 2016-08-15 26278006 Ahmad S 2015-08-17 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/26278006 A novel interaction between the FLJ33534 locus and smoking in obesity: a genome-wide study of 14 131 Pakistani adults. Body mass index variance 14,131 Pakistani ancestry individuals NA Illumina [NR] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST003087 Genome-wide genotyping array 2016-12-01 27021820 Roostaei T 2016-03-29 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27021820 Genome-wide interaction study of brain beta-amyloid burden and cognitive impairment in Alzheimer's disease. Cognitive impairment (brain beta-amyloid deposition interaction) 251 European ancestry early mild cases, 122 European ancestry late mild cases, 108 European ancestry Alzheimer's disease cases, 197 European ancestry controls 280 European ancestry mild cases, 287 European ancestry Alzheimer's disease cases, 382 European ancestry controls Illumina [NR] (imputed) 0 cerebral amyloid deposition measurement, Cognitive impairment http://www.ebi.ac.uk/efo/EFO_0007707, http://purl.obolibrary.org/obo/HP_0100543 GCST003399 Genome-wide genotyping array 2016-10-05 26644207 Clarelli F 2015-12-08 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/26644207 Pharmacogenetic study of long-term response to interferon-β treatment in multiple sclerosis. Response to interferon beta in multiple sclerosis 166 European ancestry responder cases, 171 European ancestry non-responder cases NA Illumina [1387466] (imputed) 3 response to interferon-beta http://purl.obolibrary.org/obo/GO_0035456 GCST003193 Genome-wide genotyping array 2018-09-12 27022141 Liu L 2016-03-27 Exp Biol Med (Maywood) www.ncbi.nlm.nih.gov/pubmed/27022141 Original Research: A case-control genome-wide association study identifies genetic modifiers of fetal hemoglobin in sickle cell disease. High fetal hemoglobin in sickle cell disease up to 376 African American cases, up to 360 African American controls NA Illumina [at least 498706] 1 fetal hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004576 GCST006251 Genome-wide genotyping array 2019-09-11 26546613 Gutierrez-Achury J 2016-01-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26546613 Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis. Celiac disease and Rheumatoid arthritis 371 South Asian ancestry celiac disease cases, 3,138 European ancestry celiac disease cases, 4,418 European ancestry rheumatoid arthritis cases, 509 South Asian ancestry celiac disease controls, 2,473 European ancestry celiac disease controls, 3,300 European ancestry rheumatoid arthritis controls, 8,872 celiac disease cases, 9,401 rheumatoid arthritis cases, 4,845 celiac disease controls, 9,627 rheumatoid arthritis controls NA Illumina [109572] 24 rheumatoid arthritis, celiac disease http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0001060 GCST008644 Targeted genotyping array [Immunochip] 2017-01-13 27157822 Hallberg P 2016-05-03 Lancet Diabetes Endocrinol www.ncbi.nlm.nih.gov/pubmed/27157822 Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population. Anti-thyroid drug induced agranulocytosis 38 European ancestry cases, 1 case, 5,170 European ancestry controls NA Illumina [9380034] (imputed) 6 response to anti-thyroid drug, Drug-induced agranulocytosis http://www.ebi.ac.uk/efo/EFO_0007838, http://purl.obolibrary.org/obo/HP_0012235 GCST003527 Genome-wide genotyping array 2017-01-13 27157822 Hallberg P 2016-05-03 Lancet Diabetes Endocrinol www.ncbi.nlm.nih.gov/pubmed/27157822 Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population. Non-chemotherapy drug induced agranulocytosis 222 European ancestry cases, 12 cases, 5,170 European ancestry controls NA Illumina [9380034] (imputed) 5 response to xenobiotic stimulus, Drug-induced agranulocytosis http://purl.obolibrary.org/obo/GO_0009410, http://purl.obolibrary.org/obo/HP_0012235 GCST003526 Genome-wide genotyping array 2017-01-27 27285765 Chen D 2016-06-07 Oncotarget www.ncbi.nlm.nih.gov/pubmed/27285765 Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus. Cervical cancer 1,553 Swedish ancestry cervical intraepithelial neoplasia grade 3 cases, 81 Swedish ancestry cervical cancer cases, 4,442 Swedish ancestry controls 827 Swedish ancestry cervical intraepithelial neoplasia grade 3 cases, 123 Swedish ancestry cervical cancer cases, 1,715 European ancestry controls Illumina [5471179] 1 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST003565 Genome-wide genotyping array 2016-06-28 26519441 Kim S 2015-10-30 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/26519441 Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians. Plasma homocysteine levels 853 African American cognitively normal individuals, 45 African American dementia cases, 934 Yoruban ancestry cognitively normal individuals, 26 Yoruban ancestry dementia cases NA Illumina [NR] (imputed) 1 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST003157 Genome-wide genotyping array 2017-04-05 27936112 Kalsi G 2016-12-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/27936112 Genome-Wide Association of Heroin Dependence in Han Chinese. Heroin dependence 370 Han Chinese ancestry cases, 134 Han Chinese ancestry controls Illumina [4009606] (imputed) 8 heroin dependence http://www.ebi.ac.uk/efo/EFO_0004240 GCST003878 Genome-wide genotyping array 2017-04-10 27957625 Bacchelli E 2016-12-13 J Headache Pain www.ncbi.nlm.nih.gov/pubmed/27957625 A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants. Cluster headache 99 Italian ancestry cases, 359 Italian ancestry smoker controls Illumina [290505] 2 smoking status measurement, Cluster headache http://www.ebi.ac.uk/efo/EFO_0006527, http://purl.obolibrary.org/obo/HP_0012199 GCST003900 Genome-wide genotyping array 2017-05-11 27941131 Feenstra B 2016-12-09 J Med Genet www.ncbi.nlm.nih.gov/pubmed/27941131 Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy. Tonsillectomy 1,464 Northwestern European ancestry cases and 12,019 Northwestern European ancestry controls. 1,575 Northwestern European ancestry cases and 1,367 Northwestern European ancestry controls. Illumina [7855469] (imputed) 1 tonsillectomy risk measurement http://www.ebi.ac.uk/efo/EFO_0007924 GCST003974 Genome-wide genotyping array 2017-03-31 27117709 Couch FJ 2016-04-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27117709 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Breast cancer 4,939 European ancestry estrogen receptor-negative cases, 14,352 European ancestry controls 7,333 European ancestry estrogen receptor-negative cases, 7,797 European ancestry BRCA1 mutation carrier cases, 7,455 European ancestry BRCA1 mutation carrier controls, 42,468 European ancestry controls Illumina [10909381] (imputed) 31 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST003845 Genome-wide genotyping array 2017-03-31 27117709 Couch FJ 2016-04-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27117709 Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer. Breast cancer (estrogen-receptor negative) 4,939 European ancestry cases, 14,352 European ancestry controls 7,333 European ancestry cases, 42,468 European ancestry controls Illumina [10909381] (imputed) 25 estrogen-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_1000650 GCST003842 Genome-wide genotyping array 2016-06-13 26365420 Mbarek H 2015-09-14 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26365420 The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores. Alcohol dependence 1,374 European ancestry cases and 6,468 European ancestry controls from 7,694 twin pairs NA Affymetrix, Illumina, Perlegen [6464174] (imputed) 18 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST003121 Genome-wide genotyping array 2016-09-28 26569114 Brown EL 2015-11-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/26569114 Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas. Staphylococcus aureus nasal carriage (persistent) 141 Mexican American persistent carrier individuals, 620 Mexican American non-carrier individuals NA Affymetrix, Illumina [at least 603042] (imputed) 5 persistent Staphylococcus aureus carrier status http://www.ebi.ac.uk/efo/EFO_0007757 GCST003182 Genome-wide genotyping array 2016-09-28 26569114 Brown EL 2015-11-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/26569114 Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas. Staphylococcus aureus nasal carriage (intermittent) 97 Mexican American intermittent carrier individuals, 620 Mexican American non-carrier individuals NA Affymetrix, Illumina [at least 603042] (imputed) 7 intermittent Staphylococcus aureus carrier status http://www.ebi.ac.uk/efo/EFO_0007758 GCST003181 Genome-wide genotyping array 2016-07-27 26237429 Aminkeng F 2015-08-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26237429 A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer. Anthracycline-induced cardiotoxicity in childhood cancer 32 European ancestry cases with cardiotoxicity, 248 European ancestry cases without cardiotoxicity 22 European ancestry cases with cardiotoxicity, 74 European ancestry cases without cardiotoxicity, 2 African cases with cardiotoxicity, 9 African cases without cardiotoxicity, 5 Hispanic cases with cardiotoxicity, 18 Hispanic cases without cardiotoxicity, 8 East Asian cases with cardiotoxicity, 23 East Asian cases without cardiotoxicity, 4 Aboriginal Canadian cases with cardiotoxicity, 11 Aboriginal Canadian cases without cardiotoxicity Illumina [657694] 2 cardiotoxicity, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_1001482, http://www.ebi.ac.uk/efo/EFO_0005257 GCST003062 Genome-wide genotyping array 2016-07-20 26256467 Wojczynski MK 2015-07-03 Metabolism www.ncbi.nlm.nih.gov/pubmed/26256467 Genome-wide association study of triglyceride response to a high-fat meal among participants of the NHLBI Genetics of Lipid Lowering Drugs and Diet Network (GOLDN). Postprandial triglyceride response to high fat diet meal 872 European ancestry individuals 843 Old Order Amish individuals Affymetrix, Illumina [~ 2500000] (imputed) 9 response to high fat food intake, triglyceride change measurement http://www.ebi.ac.uk/efo/EFO_0007684, http://www.ebi.ac.uk/efo/EFO_0007681 GCST003014 Genome-wide genotyping array 2016-09-13 26291516 Miller FW 2015-08-20 Genes Immun www.ncbi.nlm.nih.gov/pubmed/26291516 Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes. Myositis 1,710 European ancestry cases, 4,724 European ancestry controls NA Illumina [NR] (imputed) 23 myositis http://www.ebi.ac.uk/efo/EFO_0000783 GCST003092 Genome-wide genotyping array 2016-04-12 26289589 Nishizawa D 2015-08-20 Mol Brain www.ncbi.nlm.nih.gov/pubmed/26289589 Associations between the orexin (hypocretin) receptor 2 gene polymorphism Val308Ile and nicotine dependence in genome-wide and subsequent association studies. Nicotine dependence 148 Japanese ancestry individuals 374 Japanese ancestry individuals Illumina [225591] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST003093 Genome-wide genotyping array 2016-09-07 26323598 Brandl EJ 2015-09-01 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/26323598 Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample. Antipsychotic drug-induced weight gain 189 European ancestry treated schizophrenia cases 86 European ancestry treated schizophrenia or schizoaffective cases Illumina, Perlegen [321290] 1 antipsychotic drug related weight gain http://www.ebi.ac.uk/efo/EFO_0004567 GCST003109 Genome-wide genotyping array 2016-09-07 26323598 Brandl EJ 2015-09-01 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/26323598 Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample. Antipsychotic drug-induced weight gain (time interaction) 189 European ancestry treated schizophrenia cases NA Illumina, Perlegen [321290] 1 longitudinal BMI measurement, antipsychotic drug related weight gain http://www.ebi.ac.uk/efo/EFO_0005937, http://www.ebi.ac.uk/efo/EFO_0004567 GCST003108 Genome-wide genotyping array 2016-09-12 26394188 Zhu Z 2015-09-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26394188 Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls. Adolescent idiopathic scoliosis 960 Han Chinese ancestry cases, 1,499 Han Chinese ancestry controls 3,316 Han Chinese ancestry cases, 4,516 Han Chinese ancestry controls Affymetrix [516220] 4 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST003128 Genome-wide genotyping array 2016-10-11 26573232 Wu L 2015-11-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/26573232 A genome-wide association study identifies WT1 variant with better response to 5-fluorouracil, pirarubicin and cyclophosphamide neoadjuvant chemotherapy in breast cancer patients. Response to anthracycline-based chemotherapy in breast cancer (pathologic complete response) 30 East Asian ancestry responder cases, 62 East Asian ancestry non-responder cases 62 East Asian ancestry responder cases, 339 East Asian ancestry non-responder cases Affymetrix [389795] 0 pathologic complete response measurement, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_0007771, http://www.ebi.ac.uk/efo/EFO_0005257 GCST003224 Genome-wide genotyping array 2016-08-31 26312577 Tan LJ 2015-08-27 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/26312577 Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche. Bone mineral density (spine) and age at menarche 826 Han Chinese ancestry females 1,728 European ancestry females, 709 African American females, 408 Hispanic/Latin American females Affymetrix [702413] 9 age at menarche, spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0004703, http://www.ebi.ac.uk/efo/EFO_0007701 GCST003101 Genome-wide genotyping array 2016-09-07 26312577 Tan LJ 2015-08-27 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/26312577 Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche. Bone mineral density (hip) and age at menarche 826 Han Chinese ancestry females 1,728 European ancestry females, 709 African American females, 408 Hispanic/Latin American females Affymetrix [702413] 8 hip bone mineral density, age at menarche http://www.ebi.ac.uk/efo/EFO_0007702, http://www.ebi.ac.uk/efo/EFO_0004703 GCST003102 Genome-wide genotyping array 2016-06-29 26339675 Tosto G 2015-06-18 Ann Clin Transl Neurol www.ncbi.nlm.nih.gov/pubmed/26339675 F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease. Alzheimer's disease (late onset) 2,451 Caribbean Hispanic cases, 2,063 Caribbean Hispanic controls 550 Caribbean Hispanic cases, 236 Caribbean Hispanic controls Affymetrix, Illumina [8837542] (imputed) 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002983 Genome-wide genotyping array 2016-06-28 26293465 Durda P 2015-08-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/26293465 Plasma Levels of Soluble Interleukin-2 Receptor α: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan. Soluble interleukin-2 receptor subunit alpha 2,964 European ancestry individuals, 683 African American individuals 4,464 European ancestry individuals Illumina [2200000] (imputed) 7 soluble interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0007650 GCST003088 Genome-wide genotyping array 2016-06-17 26299439 Li WD 2015-08-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26299439 Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels. Adiponectin levels 737 European ancestry females NA Illumina [up to 550000] 5 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST003096 Genome-wide genotyping array 2016-09-12 26299439 Li WD 2015-08-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26299439 Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels. Adiponectin levels (BMI-adjusted) 737 European ancestry females NA Illumina [up to 550000] 4 BMI-adjusted adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0007737 GCST003095 Genome-wide genotyping array 2016-09-19 26433129 Tin A 2015-10-03 Diabet Med www.ncbi.nlm.nih.gov/pubmed/26433129 GCKR and PPP1R3B identified as genome-wide significant loci for plasma lactate: the Atherosclerosis Risk in Communities (ARIC) study. Plasma lactate levels 6,901 European ancestry individuals 1,671 African American individuals Affymetrix [~ 38000000] (imputed) 4 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST003147 Genome-wide genotyping array 2016-09-06 26433762 Liu X 2015-09-25 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/26433762 A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region. Eating disorder in bipolar disorder 184 European ancestry cases, 2,006 European ancestry controls NA Affymetrix [703012] 5 eating disorder http://www.ebi.ac.uk/efo/EFO_0005203 GCST003132 Genome-wide genotyping array 2016-09-06 26433762 Liu X 2015-09-25 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/26433762 A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region. Bipolar disorder and eating disorder 184 European ancestry cases with bipolar disorder and eating disorder, 1,370 European ancestry controls NA Affymetrix [703012] 10 eating disorder, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0005203, http://purl.obolibrary.org/obo/MONDO_0004985 GCST003135 Genome-wide genotyping array 2016-09-06 26433762 Liu X 2015-09-25 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/26433762 A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region. Bipolar disorder 2,006 European ancestry bipolar disorder without eating disorder cases, 1,370 European ancestry controls NA Affymetrix [703012] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST003136 Genome-wide genotyping array 2016-09-19 26417704 Corvol H 2015-09-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26417704 Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis. Lung disease severity in cystic fibrosis 4,139 European and other ancestry p.Phe508del homozygote cases, 2,226 European and other ancestry cases NA Illumina [8520458] (imputed) 29 lung disease associated with cystic fibrosis http://www.ebi.ac.uk/efo/EFO_0009797 GCST003143 Genome-wide genotyping array 2016-09-06 26422391 Yellin JL 2015-09-28 J Pediatr Orthop www.ncbi.nlm.nih.gov/pubmed/26422391 Candidate Loci are Revealed by an Initial Genome-wide Association Study of Juvenile Osteochondritis Dissecans. Juvenile osteochondritis dissecans 209 European ancestry cases, 1,855 European ancestry controls NA Illumina [NR] 5 Osteochondritis dissecans http://purl.obolibrary.org/obo/HP_0010886 GCST003138 Genome-wide genotyping array 2016-03-03 26067905 Bari R 2015-06-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26067905 Genome-wide single-nucleotide polymorphism analysis revealed SUFU suppression of acute graft-versus-host disease through downregulation of HLA-DR expression in recipient dendritic cells. Acute graft-versus-host disease in allogeneic hematopoietic stem cell transplantation 39 cases, 29 controls 45 cases, 55 controls Affymetrix [305830] 0 response to allogeneic hematopoietic stem cell transplant, acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0004599 GCST002958 Genome-wide genotyping array 2016-07-14 26098866 Helgason H 2015-06-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26098866 Loss-of-function variants in ATM confer risk of gastric cancer. Gastric cancer 2,500 European ancestry cases, 205,652 European ancestry controls (includes non-array genotyped, whole genome imputed individuals) NA Illumina [~ 25000000] (imputed) 8 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST002992 Genome-wide genotyping array 2016-07-14 26098866 Helgason H 2015-06-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26098866 Loss-of-function variants in ATM confer risk of gastric cancer. Gastric adenocarcinoma (histologically verified) 2,043 European ancestry cases, 202,533 European ancestry controls NA Illumina [~ 25000000] (imputed) 7 gastric adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000503 GCST002990 Genome-wide genotyping array 2016-07-08 26077951 Kouri N 2015-06-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26077951 Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Corticobasal degeneration 152 cases, 3,111 controls 67 cases, 457 controls Illumina [533898] (imputed) 4 corticobasal degeneration disorder http://purl.obolibrary.org/obo/MONDO_0022308 GCST002971 Genome-wide genotyping array 2016-07-08 26077951 Kouri N 2015-06-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26077951 Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. Corticobasal degeneration 152 cases, 1,986 controls NA Illumina [533898] (imputed) 4 corticobasal degeneration disorder http://purl.obolibrary.org/obo/MONDO_0022308 GCST002970 Genome-wide genotyping array 2016-08-17 26314684 Liu X 2015-08-28 Autism Res www.ncbi.nlm.nih.gov/pubmed/26314684 Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations. Autism spectrum disorder 156 Japanese ancestry cases, 620 Japanese ancestry controls 205 Japanese ancestry cases, 184 Japanese ancestry controls, 418 Han Chinese ancestry cases and 836 Han Chinese ancestry controls from 418 trios Affymetrix [561592] 1 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST003104 Genome-wide genotyping array 2016-05-17 26083657 Stafford-Smith M 2015-06-17 Kidney Int www.ncbi.nlm.nih.gov/pubmed/26083657 Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci. Acute kidney injury in coronary artery bypass surgery (creatinine rise) 873 European ancestry cases 380 European ancestry cases Illumina [530716] (imputed) 3 creatinine measurement, Acute kidney injury http://www.ebi.ac.uk/efo/EFO_0004518, http://purl.obolibrary.org/obo/HP_0001919 GCST002982 Genome-wide genotyping array 2016-05-18 26083723 Park S 2015-06-17 Blood Press www.ncbi.nlm.nih.gov/pubmed/26083723 Lack of association between arterial stiffness and genetic variants by genome-wide association scan. Arterial stiffness (pulse-wave velocity) 402 Korean ancestry individuals 1206 Korean ancestry individuals Affymetrix [502731] 0 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST002980 Genome-wide genotyping array 2016-07-11 26112879 Rudkowska I 2015-06-20 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/26112879 Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study. LDL peak particle diameter (total fat intake interaction) 541 European ancestry individuals NA Illumina [1632371] (imputed) 21 LDL peak particle diameter measurement, total fat intake measurement http://www.ebi.ac.uk/efo/EFO_0007677, http://www.ebi.ac.uk/efo/EFO_0007678 GCST002989 Genome-wide genotyping array 2016-06-08 26079190 Galfalvy H 2015-06-16 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26079190 A genome-wide association study of suicidal behavior. Suicide behavior 577 European ancestry cases, 1,233 European ancestry controls NA Illumina [794207] 5 suicide behaviour http://www.ebi.ac.uk/efo/EFO_0007623 GCST002969 Genome-wide genotyping array 2016-06-08 26079190 Galfalvy H 2015-06-16 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26079190 A genome-wide association study of suicidal behavior. Suicide ideation score in major depressive disorder 358 European ancestry individuals NA Illumina [794207] 3 suicide ideation measurement http://www.ebi.ac.uk/efo/EFO_0007619 GCST002974 Genome-wide genotyping array 2016-06-08 26079190 Galfalvy H 2015-06-16 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26079190 A genome-wide association study of suicidal behavior. Suicide 317 European ancestry cases, 1,233 European ancestry controls NA Illumina [794207] 3 suicide http://www.ebi.ac.uk/efo/EFO_0007624 GCST002973 Genome-wide genotyping array 2016-06-08 26079190 Galfalvy H 2015-06-16 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26079190 A genome-wide association study of suicidal behavior. Suicide attempts in major depressive disorder 257 European ancestry cases, 300 European ancestry controls NA Illumina [794207] 1 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST002972 Genome-wide genotyping array 2016-10-12 26546620 Xu CF 2015-11-06 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/26546620 HLA-B*57:01 Confers Susceptibility to Pazopanib-Associated Liver Injury in Patients with Cancer. Response to Pazopanib in cancer (hepatotoxicity) Up to 844 European ancestry cases, up to 325 Asian ancestry cases, up to 19 cases Up to 811 European ancestry cases, up to 114 Asian ancestry cases, up to 77 cases Illumina [6736730] (imputed) 1 response to pazopanib, serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0007779, http://www.ebi.ac.uk/efo/EFO_0004735 GCST003232 Genome-wide genotyping array 2016-10-14 26077402 de Rooy DP 2015-06-15 J Rheumatol www.ncbi.nlm.nih.gov/pubmed/26077402 Genetic Factors for the Severity of ACPA-negative Rheumatoid Arthritis in 2 Cohorts of Early Disease: A Genome-wide Study. Joint damage progression in ACPA-negative rheumatoid arthritis 262 Western European ancestry cases 253 Western European ancestry cases Illumina [244624] 1 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST003256 Genome-wide genotyping array 2016-10-07 26582766 Lu X 2015-11-18 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26582766 Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations. Cholesterol, total 8,344 Han Chinese ancestry individuals 14,739 Han Chinese ancestry individuals Affymetrix, Illumina [2573667] (imputed) 14 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST003214 Genome-wide genotyping array 2016-10-07 26582766 Lu X 2015-11-18 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26582766 Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations. LDL cholesterol 8,344 Han Chinese ancestry individuals 14,739 Han Chinese ancestry individuals Affymetrix, Illumina [2573667] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST003216 Genome-wide genotyping array 2016-10-07 26582766 Lu X 2015-11-18 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26582766 Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations. HDL cholesterol 8,344 Han Chinese ancestry individuals 14,739 Han Chinese ancestry individuals Affymetrix, Illumina [2573667] (imputed) 6 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST003215 Genome-wide genotyping array 2016-10-07 26582766 Lu X 2015-11-18 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26582766 Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations. Triglycerides 8,344 Han Chinese ancestry individuals 14,739 Han Chinese ancestry individuals Affymetrix, Illumina [2573667] (imputed) 9 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST003217 Genome-wide genotyping array 2016-11-30 26805783 Schick UM 2016-01-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26805783 Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans. Platelet count 12,491 Hispanic/Latin American individuals 7,170 Hispanic/Latin American individuals Illumina [2232944] (imputed) 13 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST003383 Genome-wide genotyping array 2016-09-27 26632684 Dong J 2015-11-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/26632684 Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults. Sense of smell 6,252 European ancestry individuals NA Affymetrix, Illumina [2543887] (imputed) 22 sensory perception of smell http://purl.obolibrary.org/obo/GO_0007608 GCST003174 Genome-wide genotyping array 2016-09-28 26589003 Federoff M 2015-11-05 Parkinsonism Relat Disord www.ncbi.nlm.nih.gov/pubmed/26589003 Genome-wide estimate of the heritability of Multiple System Atrophy. Multiple system atrophy 907 European ancestry cases, 3,866 European ancestry controls NA NR [11318628] (imputed) 0 multiple system atrophy http://www.ebi.ac.uk/efo/EFO_1001050 GCST003179 Genome-wide genotyping array 2016-09-28 26604143 Felix JF 2015-11-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26604143 Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Childhood body mass index 34,744 European ancestry children 11,313 European ancestry children Affymetrix, Illumina [2499691] (imputed) 39 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST003177 Genome-wide genotyping array 2016-11-14 26845276 Ikeda M 2016-01-01 J Clin Psychiatry www.ncbi.nlm.nih.gov/pubmed/26845276 Genome-wide environment interaction between depressive state and stressful life events. Major depressive disorder (stressful life events interaction) 308 East Asian ancestry prepressive cases, 780 East Asian ancestry non-depressive controls NA Illumina [418225] 2 unipolar depression, self rated health, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004778, http://www.ebi.ac.uk/efo/EFO_0007781 GCST003319 Genome-wide genotyping array 2016-10-14 26606652 Alarcon-Riquelme ME 2015-11-25 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/26606652 Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture. Systemic lupus erythematosus 862 Native American ancestry-enriched North American cases, 531 Native American ancestry-enriched South American cases, 1,973 Native American ancestry-enriched North American controls, 344 Native American ancestry-enriched South American controls NA Illumina [580483] (imputed) 40 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST003252 Genome-wide genotyping array 2016-11-29 27023175 Stringer S 2016-03-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27023175 Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Cannabis use 32,330 European ancestry individuals 2,660 African American individuals, 2,967 European ancestry individuals Affymetrix, Illumina [6444471] (imputed) 6 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST003382 Genome-wide genotyping array 2017-03-24 27802415 Salvi E 2016-10-31 Hypertension www.ncbi.nlm.nih.gov/pubmed/27802415 Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide. Diastolic blood pressure response to hydrochlorothiazide in hypertension 1,739 European ancestry individuals 430 African American individuals Affymetrix, Illumina [up to 2500000] (imputed) 8 response to hydrochlorothiazide, diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0005202, http://www.ebi.ac.uk/efo/EFO_0006945 GCST003805 Genome-wide genotyping array 2017-03-24 27802415 Salvi E 2016-10-31 Hypertension www.ncbi.nlm.nih.gov/pubmed/27802415 Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide. Systolic blood pressure response to hydrochlorothiazide in hypertension 1,739 European ancestry individuals 430 African American individuals Affymetrix, Illumina [up to 2500000] (imputed) 10 response to hydrochlorothiazide, systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0005202, http://www.ebi.ac.uk/efo/EFO_0006944 GCST003807 Genome-wide genotyping array 2017-02-24 27402877 Hill-Burns EM 2016-07-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27402877 Identification of genetic modifiers of age-at-onset for familial Parkinson's disease. Parkinson's disease (non-familial, age at onset) 1,554 European ancestry cases 2,363 European ancestry cases Illumina [7200000] (imputed) 0 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST003651 Genome-wide genotyping array 2017-02-24 27402877 Hill-Burns EM 2016-07-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27402877 Identification of genetic modifiers of age-at-onset for familial Parkinson's disease. Parkinson's disease (age of onset) 1985 European ancestry cases 3100 European ancestry cases Illumina [7200000] (imputed) 0 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST003653 Genome-wide genotyping array 2017-02-24 27402877 Hill-Burns EM 2016-07-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27402877 Identification of genetic modifiers of age-at-onset for familial Parkinson's disease. Parkinson's disease (familial, age at onset) 431 European ancestry cases 737 European ancestry cases Illumina [7200000] (imputed) 4 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST003652 Genome-wide genotyping array 2019-07-01 26887379 Tang W 2016-02-18 Mol Neurobiol www.ncbi.nlm.nih.gov/pubmed/26887379 Exome-Wide Association Study Identified New Risk Loci for Hirschsprung's Disease. Hirschsprung disease 167 East Asian ancestry cases, 900 East Asian ancestry controls NA Illumina [Exome array] 2 Hirschsprung disease http://purl.obolibrary.org/obo/MONDO_0018309 GCST008016 Exome genotyping array [Exome array] 2016-11-01 27179730 Allen NB 2016-01-23 Am Heart J www.ncbi.nlm.nih.gov/pubmed/27179730 Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies. Ideal cardiovascular health (clinical and behavioral) 883 European ancestry individuals with clinical and behavioral ideal cardiovascular health, 10,825 European ancestry individuals without clinical and behavioral ideal cardiovascular health 522 European ancestry individuals Affymetrix [~ 25000000] (imputed) 1 clinical and behavioural ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0007654 GCST003278 Genome-wide genotyping array 2016-11-01 27179730 Allen NB 2016-01-23 Am Heart J www.ncbi.nlm.nih.gov/pubmed/27179730 Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies. Ideal cardiovascular health (clinical) 2,242 European ancestry individuals with clinical ideal cardiovascular health, 9,466 European ancestry individuals without clinical ideal cardiovascular health 522 European ancestry individuals Affymetrix [~ 25000000] (imputed) 1 clinical ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0007653 GCST003279 Genome-wide genotyping array 2017-01-13 27135401 Cheng TH 2016-05-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27135401 Five endometrial cancer risk loci identified through genome-wide association analysis. Endometrial endometrioid carcinoma 2,082 European ancestry cases, 9,544 European ancestry controls 4,553 European ancestry cases, 27,600 European ancestry controls Illumina [up to 2300000] (imputed) 7 endometrial endometrioid carcinoma http://www.ebi.ac.uk/efo/EFO_1001514 GCST003525 Genome-wide genotyping array 2017-01-13 27135401 Cheng TH 2016-05-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27135401 Five endometrial cancer risk loci identified through genome-wide association analysis. Endometrial cancer 2,082 European ancestry endometrioid cases, 130 European ancestry cases, 9,544 European ancestry controls 4,553 European ancestry endometrioid cases, 972 European ancestry cases, 27,600 European ancestry controls Illumina [up to 2300000] (imputed) 8 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST003524 Genome-wide genotyping array 2016-12-21 27068588 Chauhan G 2016-04-07 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/27068588 Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. Ischemic stroke 3,028 European ancestry cases, 80,613 European ancestry controls 2,284 European ancestry cases, 17,184 European ancestry controls, 16,851 African unspecified, Hispanic and European ancestry cases, 32,473 African unspecified, Hispanic and European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST003492 Genome-wide genotyping array 2016-12-21 27068588 Chauhan G 2016-04-07 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/27068588 Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. Ischemic stroke (cardioembolic) 602 European ancestry cases, 80,613 European ancestry controls 579 European ancestry cases, 3,427 African unspecified, Hispanic and European ancestry cases, 18,515 European ancestry controls, 32,473 African unspecified, Hispanic and European ancestry controls Affymetrix, Illumina [NR] (imputed) 1 Ischemic stroke, cardiac embolism http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_1001493 GCST003490 Genome-wide genotyping array 2016-12-21 27068588 Chauhan G 2016-04-07 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/27068588 Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. Ischemic stroke (non-cardioembolic) 1,770 European ancestry cases, 80,613 European ancestry controls 335 European ancestry large-vessel ischaemic stroke cases, 365 European ancestry small-vessel ischaemic stroke cases, 2,346 African unspecified, Hispanic and European ancestry large-vessel ischaemic stroke cases, 3,150 African unspecified, Hispanic and European ancestry small-vessel ischaemic stroke cases, 18,515 European ancestry controls, 32,473 African unspecified, Hispanic and European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST003493 Genome-wide genotyping array 2016-12-21 27068588 Chauhan G 2016-04-07 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/27068588 Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies. Stroke 4,348 European ancestry cases, 80,613 European ancestry controls 681 European ancestry cases, 1,331 European ancestry controls Affymetrix, Illumina [NR] (imputed) 1 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST003491 Genome-wide genotyping array 2017-02-24 27036123 van Leeuwen EM 2016-04-01 J Med Genet www.ncbi.nlm.nih.gov/pubmed/27036123 Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. Triglycerides 41,142 European ancestry individuals, 705 East Asian ancestry individuals, 6,287 African American individuals, 1,415 Hispanic individuals 60,827 European ancestry individuals, 9,982 Indian Asian ancestry individuals, 2,710 African American/Afro-Caribbean individuals Affymetrix, Illumina [NR] (imputed) 29 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST003661 Genome-wide genotyping array 2017-02-24 27036123 van Leeuwen EM 2016-04-01 J Med Genet www.ncbi.nlm.nih.gov/pubmed/27036123 Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. LDL cholesterol 40,473 European ancestry individuals, 689 East Asian ancestry individuals, 6,237 African American individuals, 1,381 Hispanic individuals 60,078 European ancestry individuals, 9,729 Indian Asian ancestry individuals, 2,679 African American/Afro-Caribbean individuals Affymetrix, Illumina [NR] (imputed) 31 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST003662 Genome-wide genotyping array 2017-02-24 27036123 van Leeuwen EM 2016-04-01 J Med Genet www.ncbi.nlm.nih.gov/pubmed/27036123 Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. Cholesterol, total 51,430 European ancestry individuals, 702 East Asian ancestry individuals, 6,480 African American individuals, 1,412 Hispanic individuals 71,032 European ancestry individuals, 10,000 Indian Asian ancestry individuals, 2,707 African American/Afro-Caribbean individuals Affymetrix, Illumina [NR] (imputed) 45 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST003663 Genome-wide genotyping array 2017-02-24 27036123 van Leeuwen EM 2016-04-01 J Med Genet www.ncbi.nlm.nih.gov/pubmed/27036123 Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels. HDL cholesterol 50,823 European ancestry individuals, 703 East Asian ancestry individuals, 6,476 African American individuals, 1,407 Hispanic individuals 71,921 European ancestry individuals, 9,992 Indian Asian ancestry individuals, 2,685 African American/Afro-Caribbean individuals Affymetrix, Illumina [NR] (imputed) 37 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST003660 Genome-wide genotyping array 2017-02-21 27193062 Adhikari K 2016-05-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27193062 A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. middle facial morphology traits (ordinal measurement) 5,958 Latin American ancestry individuals 501 Latin American ancestry individuals Illumina [9117642] (imputed) 0 nose morphology measurement, cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843, http://www.ebi.ac.uk/efo/EFO_0007847 GCST003633 Genome-wide genotyping array 2017-02-21 27193062 Adhikari K 2016-05-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27193062 A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. lower facial morphology traits (ordinal measurement) 5,958 Latin American ancestry individuals. NA Illumina [9117642] (imputed) 0 lip morphology measurement, chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845, http://www.ebi.ac.uk/efo/EFO_0007842 GCST003634 Genome-wide genotyping array 2017-02-21 27193062 Adhikari K 2016-05-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27193062 A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. middle facial morphology traits (quantitative measurement) 2955 Latin American ancestry individuals. NA Illumina [9117642] (imputed) 7 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST003635 Genome-wide genotyping array 2017-02-21 27193062 Adhikari K 2016-05-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27193062 A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. lower facial morphology traits (quantitative measurement) 2955 Latin American ancestry individuals. NA Illumina [9117642] (imputed) 1 lip morphology measurement, chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845, http://www.ebi.ac.uk/efo/EFO_0007842 GCST003636 Genome-wide genotyping array 2017-02-21 27193062 Adhikari K 2016-05-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27193062 A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. facial morphology traits (multivariate analysis) 5,958 Latin American ancestry individuals. NA Illumina [9117642] (imputed) 4 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST003637 Genome-wide genotyping array 2017-02-21 27193062 Adhikari K 2016-05-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27193062 A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation. upper facial morphology traits (ordinal measurement) 5,958 Latin American ancestry individuals. NA Illumina [9117642] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST003638 Genome-wide genotyping array 2016-12-01 27333618 Sekula P 2016-02-04 Nephrol Dial Transplant www.ncbi.nlm.nih.gov/pubmed/27333618 Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies. Membranous nephropathy 323 European ancestry cases, 345 European ancestry controls 137 European ancestry cases, 379 European ancestry controls Illumina [8968426] (imputed) 2 membranous glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004254 GCST003402 Genome-wide genotyping array 2017-01-10 27354352 Han MR 2016-06-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27354352 Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci. Breast cancer 7,619 East Asian ancestry cases, 6,286 East Asian ancestry controls 6,605 East Asian ancestry cases, 8,543 East Asian ancestry controls Affymetrix, Illumina [668499] (imputed) 8 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST003520 Genome-wide genotyping array 2017-02-24 27315593 Lang M 2016-06-14 Eur Psychiatry www.ncbi.nlm.nih.gov/pubmed/27315593 Genome-wide association study of pathological gambling. Pathological gambling 445 European ancestry cases, 986 European ancestry controls NA Illumina [595867] 3 pathological gambling http://www.ebi.ac.uk/efo/EFO_1001926 GCST003648 Genome-wide genotyping array 2017-03-10 27329760 Hou L 2016-06-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27329760 Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Bipolar disorder 7,647 European ancestry cases, 27,303 European ancestry controls 2,137 European ancestry cases, 3,168 European ancestry controls Affymetrix, Illumina [9692718] (imputed) 6 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST003724 Genome-wide genotyping array 2016-12-21 27046643 Davies G 2016-04-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27046643 Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151). Memory performance 112,067 European ancestry individuals NA Affymetrix [~ 17300000] (imputed) 0 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST003497 Genome-wide genotyping array 2016-12-21 27046643 Davies G 2016-04-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27046643 Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151). Verbal-numerical reasoning 36,035 European ancestry individuals NA Affymetrix [~ 17300000] (imputed) 3 reasoning http://www.ebi.ac.uk/efo/EFO_0004350 GCST003498 Genome-wide genotyping array 2016-12-21 27046643 Davies G 2016-04-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27046643 Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151). Educational attainment 111,114 European ancestry individuals NA Affymetrix [~ 17300000] (imputed) 15 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST003496 Genome-wide genotyping array 2016-12-21 27046643 Davies G 2016-04-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27046643 Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151). Reaction time 111,483 European ancestry individuals NA Affymetrix [~ 17300000] (imputed) 2 reaction time measurement http://www.ebi.ac.uk/efo/EFO_0008393 GCST003499 Genome-wide genotyping array 2017-01-25 27311723 Pei YF 2016-06-16 Osteoporos Int www.ncbi.nlm.nih.gov/pubmed/27311723 Association of 3q13.32 variants with hip trochanter and intertrochanter bone mineral density identified by a genome-wide association study. Bone mineral density (hip) 6,912 European ancestry individuals 845 African American individuals, 446 Hispanic individuals, 971 European ancestry individuals Affymetrix [6879267] (imputed) 4 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST003559 Genome-wide genotyping array 2017-03-10 27322543 Gormley P 2016-06-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27322543 Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Migraine 59,674 European ancestry cases, 316,078 European ancestry controls NA Affymetrix, Illumina, Perlegen [8094889] (imputed) 44 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST003720 Genome-wide genotyping array 2017-03-10 27322543 Gormley P 2016-06-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27322543 Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Migraine without aura 8,348 European ancestry cases, 139,622 European ancestry controls NA Affymetrix, Illumina, Perlegen [8094889] (imputed) 7 migraine without aura, susceptibility to, 4 http://purl.obolibrary.org/obo/MONDO_0011847 GCST003721 Genome-wide genotyping array 2017-03-10 27322543 Gormley P 2016-06-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27322543 Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Migraine with aura 6,332 European ancestry cases, 144,883 European ancestry controls NA Affymetrix, Illumina, Perlegen [8094889] (imputed) 0 migraine with aura http://purl.obolibrary.org/obo/MONDO_0005475 GCST003722 Genome-wide genotyping array 2017-02-24 27236921 Rautanen A 2016-06-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27236921 Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children. Pneumococcal bacteremia 429 African ancestry cases, 2,677 African ancestry controls 113 African ancestry cases, 1,336 African ancestry controls Affymetrix [up to 10996499] (imputed) 9 pneumococcal bacteremia http://www.ebi.ac.uk/efo/EFO_1001925 GCST003649 Genome-wide genotyping array 2017-02-24 27236921 Rautanen A 2016-06-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27236921 Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children. Bacteremia 1,536 African ancestry cases, 2,677 African ancestry controls 434 African ancestry cases, 1,336 African ancestry controls Affymetrix [up to 10996499] (imputed) 12 bacteriemia http://www.ebi.ac.uk/efo/EFO_0003033 GCST003650 Genome-wide genotyping array 2017-02-20 27485664 Bonfiglio F 2016-08-03 Neurogastroenterol Motil www.ncbi.nlm.nih.gov/pubmed/27485664 A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population. Gastroesophageal reflux disease 2,247 European ancestry cases, 4,503 European ancestry controls NA Illumina [2327020] (imputed) 7 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST003631 Genome-wide genotyping array 2017-02-10 27503288 Song IW 2016-08-08 Hum Genet www.ncbi.nlm.nih.gov/pubmed/27503288 Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study. Sjögren's syndrome 242 Han Chinese ancestry cases, 1,444 Han Chinese ancestry controls 178 Han Chinese ancestry cases, 14,432 Han Chinese ancestry controls Affymetrix [548825] (imputed) 1 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST003604 Genome-wide genotyping array 2016-12-22 27114598 Liu C 2016-04-25 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/27114598 Clinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia. Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia 71 cases with pancreatitis, 142 cases without pancreatitis NA Affymetrix [at least 751455] 0 asparaginase-induced acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1001507 GCST003500 Genome-wide genotyping array 2016-12-22 27114598 Liu C 2016-04-25 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/27114598 Clinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia. Asparaginase-induced acute pancreatitis in acute lymphoblastic leukemia (onset time) 46 European ancestry cases with pancreatitis, 3,023 European ancestry cases without pancreatitis, 11 Black cases with pancreatitis, 339 Black cases without pancreatitis, 46 Hispanic cases with pancreatitis, 1,131 Hispanic cases without pancreatitis, 1 Asian ancestry case with pancreatitis, 98 Asian ancestry cases without pancreatitis, 13 cases with with pancreatitis, 477 cases without pancreatitis NA Affymetrix [at least 751455] 11 asparaginase-induced acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1001507 GCST003501 Genome-wide genotyping array 2017-02-19 27488534 Patel YM 2016-08-03 Cancer Res www.ncbi.nlm.nih.gov/pubmed/27488534 Novel Association of Genetic Markers Affecting CYP2A6 Activity and Lung Cancer Risk. Nicotine metabolite ratio in current smokers 437 European ancestry individuals, 364 African American individuals, 453 Latino individuals, 674 Japanese American individuals, 311 Native Hawaiian ancestry individuals NA Illumina [11892802] (imputed) 14 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST003629 Genome-wide genotyping array 2017-02-03 27327535 Laville V 2016-06-21 Pigment Cell Melanoma Res www.ncbi.nlm.nih.gov/pubmed/27327535 A genome-wide association study in Caucasian women suggests the involvement of HLA genes in the severity of facial solar lentigines. Severity of facial solar lentigines 502 French ancestry individuals Illumina [795063] 2 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST003591 Genome-wide genotyping array 2017-03-20 27492634 Du Y 2016-08-01 Endocr Relat Cancer www.ncbi.nlm.nih.gov/pubmed/27492634 Genetic associations with neuroendocrine tumor risk: results from a genome-wide association study. Neuroendocrine tumor 832 European ancestry cases, 4,542 European ancestry controls. NA Affymetrix [613218] 0 neuroendocrine neoplasm http://www.ebi.ac.uk/efo/EFO_1001901 GCST003785 Genome-wide genotyping array 2017-03-20 27492634 Du Y 2016-08-01 Endocr Relat Cancer www.ncbi.nlm.nih.gov/pubmed/27492634 Genetic associations with neuroendocrine tumor risk: results from a genome-wide association study. Small intestine neuroendocrine tumor 293 European ancestry cases, 4,542 European ancestry controls, up to 241 controls NA Affymetrix [613218] 1 small intestine neuroendocrine tumor http://www.ebi.ac.uk/efo/EFO_1001928 GCST003786 Genome-wide genotyping array 2017-03-20 27492634 Du Y 2016-08-01 Endocr Relat Cancer www.ncbi.nlm.nih.gov/pubmed/27492634 Genetic associations with neuroendocrine tumor risk: results from a genome-wide association study. Pancreatic neuroendocrine tumor 156 European ancestry cases, 4,542 European ancestry controls NA Affymetrix [613218] 0 pancreatic neuroendocrine tumor http://www.ebi.ac.uk/efo/EFO_1000045 GCST003788 Genome-wide genotyping array 2017-03-20 27492634 Du Y 2016-08-01 Endocr Relat Cancer www.ncbi.nlm.nih.gov/pubmed/27492634 Genetic associations with neuroendocrine tumor risk: results from a genome-wide association study. Bronchial neuroendocrine tumor 128 European ancestry cases, 4,542 European ancestry controls NA Affymetrix [613218] 1 pulmonary neuroendocrine tumor http://www.ebi.ac.uk/efo/EFO_0005220 GCST003787 Genome-wide genotyping array 2017-03-30 27494321 Jones SE 2016-08-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27494321 Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. Chronotype 127,898 British individuals 89,283 individuals NR [16760980] (imputed) 14 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST003837 Genome-wide genotyping array 2017-03-30 27494321 Jones SE 2016-08-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27494321 Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. Sleep duration 127,573 British individuals 47,180 individuals NR [16761225] (imputed) 3 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST003839 Genome-wide genotyping array 2017-03-30 27494321 Jones SE 2016-08-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27494321 Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. Morning vs. evening chronotype 114,765 British individuals NA NR [16760980] (imputed) 15 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST003838 Genome-wide genotyping array 2017-03-30 27494321 Jones SE 2016-08-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27494321 Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. Sleep duration (oversleepers vs undersleepers) 10,102 British oversleeper individuals, 28,980 British undersleeper indivdiuals NA NR [16761225] (imputed) 2 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST003840 Genome-wide genotyping array 2018-12-07 27494321 Jones SE 2016-08-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27494321 Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. Sleep duration (oversleepers) 10,102 British ancestry cases, 81,204 British ancestry controls NA NR [16761225] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST006685 Genome-wide genotyping array 2018-12-07 27494321 Jones SE 2016-08-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/27494321 Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. Sleep duration (undersleepers) 28,980 British ancestry cases, 81,208 British ancestry controls NA NR [16761225] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST006686 Genome-wide genotyping array 2017-02-10 27501781 Shiraishi K 2016-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27501781 Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma. EGFR mutation-positive lung adenocarcinoma 663 Japanese ancestry cases, 4,367 Japanese ancestry controls 2,510 Japanese ancestry cases, 10,791 Japanese ancestry controls Illumina [NR] (imputed) 6 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST003605 Genome-wide genotyping array 2017-02-13 27480026 Liu X 2016-08-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27480026 Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension. Hypertension 271 Chinese ancestry cases, 247 Chinese ancestry controls 9,633 Chinese ancestry cases, 11,839 Chinese ancestry controls Illumina [727172] 1 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST003613 Genome-wide genotyping array 2016-12-16 26708285 Wakil SM 2016-02-01 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/26708285 A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. Coronary artery disease 2,165 Saudi Arab ancestry cases, 2,266 Saudi Arab ancestry controls 503 Saudi Arab ancestry cases, 734 Saudi Arab ancestry controls Affymetrix [537798] 9 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST003470 Genome-wide genotyping array 2016-12-16 26708285 Wakil SM 2016-02-01 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/26708285 A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs. Myocardial infarction 2,563 Saudi Arab ancestry cases, 1,868 Saudi Arab ancestry controls 866 Saudi Arab ancestry cases, 371 Saudi Arab ancestry controls Affymetrix [537798] 9 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST003471 Genome-wide genotyping array 2017-05-12 27911795 Schumann G 2016-11-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/27911795 KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference. Alcohol consumption up to 70,460 European ancestry drinker individuals up to 35,438 European ancestry drinker individuals Affymetrix, Illumina, Perlegen [at least 316407] (imputed) 3 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST004026 Genome-wide genotyping array 2017-05-12 27911795 Schumann G 2016-11-28 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/27911795 KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference. Alcohol consumption (heavy vs. light/non-drinkers) up to 74,711 European ancestry heavy and light/non-drinker individuals up to 31,021 European ancestry heavy and light/non-drinker individuals Affymetrix, Illumina, Perlegen [at least 316407] (imputed) 2 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST004027 Genome-wide genotyping array 2017-02-24 27397699 Pei YF 2016-07-07 Bone www.ncbi.nlm.nih.gov/pubmed/27397699 Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density. Bone mineral density (Ward's triangle area) 4,305 European ancestry individuals,1,579 Chinese Han ancestry individuals, 845 African-American individuals, 446 Hispanic individuals Affymetrix, Illumina [at least 9551331] (imputed) 18 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST003654 Genome-wide genotyping array 2017-03-30 27529621 Otowa T 2016-08-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/27529621 The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population. Depressive symptoms 320 Japanese ancestry individuals 439 Japanese ancestry individuals Affymetrix [534848] 1 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST003836 Genome-wide genotyping array 2017-03-30 27529621 Otowa T 2016-08-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/27529621 The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population. Depressive symptoms (stressful life events interaction) 320 Japanese ancestry individuals 439 Japanese ancestry individuals Affymetrix [534848] 4 depressive symptom measurement, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007781 GCST003835 Genome-wide genotyping array 2016-12-09 27043157 Keers R 2016-04-05 Psychother Psychosom www.ncbi.nlm.nih.gov/pubmed/27043157 A Genome-Wide Test of the Differential Susceptibility Hypothesis Reveals a Genetic Predictor of Differential Response to Psychological Treatments for Child Anxiety Disorders. Discordance in emotional problems in monozygotic twins up to 1,026 child monozygotic twin pairs NA Affymetrix [679050] 6 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST003437 Genome-wide genotyping array 2016-12-13 27023328 Kulkarni D 2016-03-29 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/27023328 Pyrexia in dabrafenib-treated melanoma patients is not associated with common genetic variation or HLA polymorphisms. Adverse response to dabrafenib or dabrafenib-trametinib treatment in melanoma (pyrexia) 218 European ancestry cases with pyrexia, 361 European ancestry exposed cases without pyrexia NA Affymetrix, Illumina [6000000] (imputed) 0 response to trametinib, Fever, response to dabrafenib http://www.ebi.ac.uk/efo/EFO_0007816, http://purl.obolibrary.org/obo/HP_0001945, http://www.ebi.ac.uk/efo/EFO_0007815 GCST003456 Genome-wide genotyping array 2017-05-12 27958378 Floyd JS 2016-12-13 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/27958378 Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group. QT interval (sulfonylurea treatment interaction) 2,095 European ancestry exposed individuals, 42,907 European ancestry unexposed individuals, 1,167 African American exposed individuals, 10,564 African American unexposed individuals, 794 Hispanic/Latino American exposed individuals, 14,330 Hispanic/Latino American unexposed individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 12 response to sulfonylurea, QT interval http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0004682 GCST004031 Genome-wide genotyping array 2017-05-12 27958378 Floyd JS 2016-12-13 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/27958378 Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group. JT interval (sulfonylurea treatment interaction) 2,095 European ancestry exposed individuals, 42,907 European ancestry unexposed individuals, 1,167 African American exposed individuals, 10,564 African American unexposed individuals, 794 Hispanic/Latino American exposed individuals, 14,330 Hispanic/Latino American unexposed individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 14 JT interval, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0007885, http://www.ebi.ac.uk/efo/EFO_0007922 GCST004032 Genome-wide genotyping array 2017-05-12 27958378 Floyd JS 2016-12-13 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/27958378 Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group. QRS interval (sulfonylurea treatment interaction) 2,095 European ancestry exposed individuals, 42,907 European ancestry unexposed individuals, 1,167 African American exposed individuals, 10,564 African American unexposed individuals, 794 Hispanic/Latino American exposed individuals, 14,330 Hispanic/Latino American unexposed individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 18 QRS duration, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0005055, http://www.ebi.ac.uk/efo/EFO_0007922 GCST004033 Genome-wide genotyping array 2017-01-16 27897004 Verma SS 2016-01-01 Pac Symp Biocomput www.ncbi.nlm.nih.gov/pubmed/27897004 IDENTIFYING GENETIC ASSOCIATIONS WITH VARIABILITY IN METABOLIC HEALTH AND BLOOD COUNT LABORATORY VALUES: DIVING INTO THE QUANTITATIVE TRAITS BY LEVERAGING LONGITUDINAL DATA FROM AN EHR. Clinical laboratory measurements 17,347 European ancestry individuals 17,348 European ancestry individuals Illumina [629274] 8 alkaline phosphatase measurement, calcium measurement, hemoglobin measurement, clinical laboratory measurement, mean corpuscular hemoglobin, glucose measurement, erythrocyte measurement, bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004533, http://www.ebi.ac.uk/efo/EFO_0004838, http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004297, http://www.ebi.ac.uk/efo/EFO_0004527, http://www.ebi.ac.uk/efo/EFO_0004468, http://www.ebi.ac.uk/efo/EFO_0005047, http://www.ebi.ac.uk/efo/EFO_0004570 GCST003540 Genome-wide genotyping array 2017-04-21 27915449 Corre T 2016-12-03 Pflugers Arch www.ncbi.nlm.nih.gov/pubmed/27915449 Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine. Urinary electrolytes (magnesium/calcium ratio) 7,498 European ancestry individuals, 1,541 Val Borbera (founder/genetic isolated) individuals, 281 Carlantino (founder/genetic isolated) individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 3 magnesium:calcium ratio http://www.ebi.ac.uk/efo/EFO_0007903 GCST003929 Genome-wide genotyping array 2017-02-25 27387956 Murk W 2016-07-07 BMC Genet www.ncbi.nlm.nih.gov/pubmed/27387956 Genome-wide search identifies a gene-gene interaction between 20p13 and 2q14 in asthma. Asthma (SNP x SNP interaction) 802 European ancestry cases, 823 European ancestry controls 754 European ancestry cases, 57 European and unknown ancestry cases, 2,573 cases, 880 European ancestry controls, 68 European and unknown ancestry controls, 2,145 controls Illumina [301547] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003682 Genome-wide genotyping array 2017-02-03 27262462 Teerlink CC 2016-06-04 Hum Genet www.ncbi.nlm.nih.gov/pubmed/27262462 Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21. Prostate cancer 2,511 European ancestry cases, 1,382 European ancestry controls NA Illumina [~ 9400000] (imputed) 9 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST003586 Genome-wide genotyping array 2017-02-03 27262462 Teerlink CC 2016-06-04 Hum Genet www.ncbi.nlm.nih.gov/pubmed/27262462 Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21. Aggressive prostate cancer 1,394 European ancestry aggressive cases, 1,117 European ancestry less-aggressive cases NA Illumina [~ 9400000] (imputed) 0 cancer aggressiveness measurement, prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0006999, http://www.ebi.ac.uk/efo/EFO_0001663 GCST003585 Genome-wide genotyping array 2016-12-13 27067015 Smith DJ 2016-04-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27067015 Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci. Neuroticism 91,370 European ancestry individuals, 15,346 individuals NA Affymetrix [7207648] (imputed) 13 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST003447 Genome-wide genotyping array 2017-04-05 27927781 Robinson-Cohen C 2016-12-07 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27927781 Genetic Variants Associated with Circulating Parathyroid Hormone. Serum parathyroid hormone levels up to 22,653 European ancestry individuals. 6,502 European ancestry individuals. Affymetrix, Illumina, Perlegen [8559187] (imputed) 6 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST003879 Genome-wide genotyping array 2016-12-11 27060151 Magrangeas F 2016-04-08 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/27060151 A Genome-Wide Association Study Identifies a Novel Locus for Bortezomib-Induced Peripheral Neuropathy in European Patients with Multiple Myeloma. Bortezomib-induced peripheral neuropathy in multiple myeloma 155 French ancestry cases, 314 French ancestry controls 40 European ancestry cases, 74 European ancestry controls Affymetrix [370605] 0 peripheral neuropathy, response to bortezomib http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0007808 GCST003438 Genome-wide genotyping array 2016-12-13 27005419 Borne Y 2016-03-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27005419 Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers. Erythrocyte cadmium concentration 2,704 ever-smoker individuals, 1,728 never-smoker individuals NA Illumina [658884] 5 erythrocyte cadmium measurement http://www.ebi.ac.uk/efo/EFO_0007807 GCST003449 Genome-wide genotyping array 2016-12-13 27005419 Borne Y 2016-03-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27005419 Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers. Erythrocyte cadmium concentration in never smokers 1,728 individuals NA Illumina [658884] 7 erythrocyte cadmium measurement http://www.ebi.ac.uk/efo/EFO_0007807 GCST003448 Genome-wide genotyping array 2016-07-01 26227905 Hu Y 2015-07-31 Mol Neurobiol www.ncbi.nlm.nih.gov/pubmed/26227905 A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland. Parkinson's disease 250 Han Chinese ancestry cases, 250 Han Chinese ancestry controls NA Illumina [862198] 22 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST003059 Genome-wide genotyping array 2016-09-07 26398136 Kuo PH 2015-09-23 PLoS One www.ncbi.nlm.nih.gov/pubmed/26398136 Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population. Autism spectrum disorder 315 Han Chinese ancestry cases, 1,115 Han Chinese ancestry controls 282 Han Chinese ancestry cases, 480 Han Chinese ancestry controls Affymetrix [546171] 4 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST003130 Genome-wide genotyping array 2016-09-06 26362575 van den Berg SM 2015-09-11 Behav Genet www.ncbi.nlm.nih.gov/pubmed/26362575 Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Extraversion 63,030 European ancestry individuals 9,783 European ancestry individuals Affymetrix, Illumina, Perlegen [6941603] (imputed) 0 extraversion http://www.ebi.ac.uk/efo/EFO_0004317 GCST003120 Genome-wide genotyping array 2016-10-06 26566055 Mieda T 2015-11-13 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/26566055 Genome-wide association study identifies candidate loci associated with postoperative fentanyl requirements after laparoscopic-assisted colectomy. Fentanyl consumption in laparoscopic-assisted colectomy (first 24 hours) 116 Japanese ancestry individuals 234 Japanese ancestry individuals Illumina [921239] 1 post-operative fentanyl consumption measurement http://www.ebi.ac.uk/efo/EFO_0007770 GCST003200 Genome-wide genotyping array 2016-09-12 26343387 Nikpay M 2015-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26343387 A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Coronary artery disease 42,096 European ancestry cases, 361 African American cases, 758 Hispanic American cases, 12,658 South Asian ancestry cases, 1,802 Lebanese ancestry cases, 3,614 East Asian ancestry cases, 99,121 European ancestry controls, 2,778 African American controls, 3,337 Hispanic American controls, 12,899 South Asian ancestry controls, 466 Lebanese ancestry controls, 7,709 East Asian ancestry controls NA Affymetrix, Illumina [8600000] (imputed) 45 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST003116 Genome-wide genotyping array 2016-09-12 26343387 Nikpay M 2015-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26343387 A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease. Myocardial infarction 27,509 European ancestry cases, 130 African American cases, 278 Hispanic American cases, 10,257 South Asian ancestry cases, 288 Lebanese ancestry cases, 1,687 East Asian ancestry cases, 99,121 European ancestry controls, 2,778 African American controls, 3,337 Hispanic American controls, 12,899 South Asian ancestry controls, 466 Lebanese ancestry controls, 7,709 East Asian ancestry controls NA Affymetrix, Illumina [8600000] (imputed) 38 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST003117 Genome-wide genotyping array 2016-06-02 26207136 Cho CH 2015-07-06 Psychiatry Investig www.ncbi.nlm.nih.gov/pubmed/26207136 CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis. Hypersomnia during a major depressive episode in bipolar disorder 263 European ancestry cases with hypersomnia, 112 European ancestry cases without hypersomnia NA Affymetrix [703012] 1 major depressive episode, hypersomnia http://www.ebi.ac.uk/efo/EFO_0007634, http://www.ebi.ac.uk/efo/EFO_0005246 GCST003016 Genome-wide genotyping array 2016-01-15 26114229 Ashley-Koch AE 2015-06-12 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/26114229 Genome-wide association study of posttraumatic stress disorder in a cohort of Iraq-Afghanistan era veterans. Post-traumatic stress disorder 949 non-Hispanic black individuals, 759 European ancestry individuals NA Illumina [up to 5616481] (imputed) 9 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST002963 Genome-wide genotyping array 2016-06-08 26129866 Hu N 2015-06-30 Gut www.ncbi.nlm.nih.gov/pubmed/26129866 Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours. Gastric cancer 2,350 East Asian ancestry cases, 2,708 East Asian ancestry controls 7,408 East Asian ancestry cases, 7,548 East Asian ancestry controls Illumina [556896] 4 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST003010 Genome-wide genotyping array 2016-06-08 26129866 Hu N 2015-06-30 Gut www.ncbi.nlm.nih.gov/pubmed/26129866 Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours. Cardia gastric cancer 1,189 East Asian ancestry cases, 2,708 East Asian ancestry controls 3,738 East Asian ancestry cases, 7,548 East Asian ancestry controls Illumina [556896] 1 gastric cardia carcinoma http://www.ebi.ac.uk/efo/EFO_1001252 GCST003009 Genome-wide genotyping array 2016-06-08 26129866 Hu N 2015-06-30 Gut www.ncbi.nlm.nih.gov/pubmed/26129866 Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours. Non-cardia gastric cancer 1,027 East Asian ancestry cases, 2,708 East Asian ancestry controls 3,663 East Asian ancestry cases, 7,548 East Asian ancestry controls Illumina [556896] 2 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST003007 Genome-wide genotyping array 2016-06-29 26151496 Chen PL 2015-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26151496 Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. Thionamide-induced agranulocytosis in Graves' disease 21 East Asian ancestry cases with agranulocytosis, 662 East Asian ancestry cases without agranulocytosis 21 East Asian ancestry cases with agranulocytosis, 546 East Asian ancestry cases without agranulocytosis Affymetrix [522980] 9 response to thioamide, Drug-induced agranulocytosis http://www.ebi.ac.uk/efo/EFO_0007633, http://purl.obolibrary.org/obo/HP_0012235 GCST003018 Genome-wide genotyping array 2016-10-14 26562150 Seldin MF 2015-10-10 Mol Med www.ncbi.nlm.nih.gov/pubmed/26562150 Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations. Late-onset myasthenia gravis 532 European ancestry cases, 2,128 European ancestry controls NA Illumina [6175472] (imputed) 21 late-onset myasthenia gravis http://www.ebi.ac.uk/efo/EFO_1001490 GCST003251 Genome-wide genotyping array 2016-06-08 26116289 Raginis-Zborowska A 2015-06-24 Exp Gerontol www.ncbi.nlm.nih.gov/pubmed/26116289 Genetic determinants of swallowing impairments among community dwelling older population. Dysphagia 71 European ancestry older adult cases, 484 European ancestry older adult controls NA Illumina [4196861] (imputed) 19 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST002995 Genome-wide genotyping array 2016-12-13 27020472 Fan Q 2016-03-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27020472 Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Spherical equivalent (joint analysis main effects and education interaction) 2,604 Erasmus Rucphen population isolate individuals, 456 Sardinian population isolate individuals, 36,976 European ancestry individuals, 5,971 East Asian ancestry individuals, 2,256 Malay ancestry individuals, 2,088 Indian ancestry individuals NA Affymetrix, Illumina [up to 7331415] (imputed) 48 refractive error, self reported educational attainment http://purl.obolibrary.org/obo/MONDO_0004892, http://www.ebi.ac.uk/efo/EFO_0004784 GCST003455 Genome-wide genotyping array 2016-12-14 27028160 Sherva R 2016-03-30 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/27028160 Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. Cannabis dependence symptom count Up to 6,000 African American ancestry individuals, 8,754 European ancestry individuals At least 1,893 European ancestry individuals Illumina [NR] (imputed) 30 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST003465 Genome-wide genotyping array 2016-12-19 26959369 Haiman CA 2016-03-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/26959369 Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort. S-phenylmercapturic acid levels in smokers 364 African American current smoker individuals, 311 Native Hawaiian ancestry current smoker individuals, 437 European ancestry current smoker individuals, 453 Latino ancestry current smoker individuals, 674 Japanese American ancestry current smoker individuals NA Illumina [11892802] (imputed) 3 urinary S-phenylmercapturic acid measurement http://www.ebi.ac.uk/efo/EFO_0007651 GCST003483 Genome-wide genotyping array 2017-03-28 27764800 Cox DG 2016-10-14 Oncotarget www.ncbi.nlm.nih.gov/pubmed/27764800 GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients. Estrogen receptor status in HER2 positive breast cancer 1,944 French ancestry estrogen receptor positive cases, 1,331 French ancestry estrogen receptor negative cases NA Illumina [914144] (imputed) 0 estrogen receptor status http://www.ebi.ac.uk/efo/EFO_0005512 GCST003822 Genome-wide genotyping array 2017-03-28 27764800 Cox DG 2016-10-14 Oncotarget www.ncbi.nlm.nih.gov/pubmed/27764800 GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients. Estrogen receptor status in HER2 negative breast cancer 4,267 French ancestry estrogen receptor positive cases, 1,185 French ancestry estrogen receptor negative cases NA Illumina [914144] (imputed) 1 estrogen receptor status http://www.ebi.ac.uk/efo/EFO_0005512 GCST003823 Genome-wide genotyping array 2017-03-28 27764800 Cox DG 2016-10-14 Oncotarget www.ncbi.nlm.nih.gov/pubmed/27764800 GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients. Estrogen receptor status in breast cancer 6,211 French ancestry estrogen receptor positive cases, 2,516 French ancestry estrogen receptor negative cases NA Illumina [914144] (imputed) 1 estrogen receptor status http://www.ebi.ac.uk/efo/EFO_0005512 GCST003821 Genome-wide genotyping array 2018-07-13 26525574 Westerlind H 2015-11-02 Gut www.ncbi.nlm.nih.gov/pubmed/26525574 Dense genotyping of immune-related loci identifies HLA variants associated with increased risk of collagenous colitis. Collagenous colitis 247 European ancestry cases, 3969 European ancestry controls 67 European ancestry cases, 330 European ancestry controls Illumina [110634] 1 collagenous colitis http://www.ebi.ac.uk/efo/EFO_1001293 GCST005879 Targeted genotyping array [Immunochip] 2017-02-24 27296613 Salinas YD 2016-06-13 BMC Genet www.ncbi.nlm.nih.gov/pubmed/27296613 Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans. Body mass index 1,235 Hispanic individuals, 706 Asian ancestry individuals, 1,549 African American individuals, 2,395 European ancestry individuals 3,379 Hispanic individuals, 6,871 African American individuals Affymetrix [up to 871948] 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST003647 Genome-wide genotyping array 2017-04-05 27922604 Yu H 2016-12-06 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27922604 Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population. Schizophrenia 4,384 Han Chinese ancestry cases and 5,770 Han Chinese ancestry controls 4,339 Han Chinese ancestry cases and 7,043 Han Chinese ancestry controls Illumina [at least 473583] (imputed) 9 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST003880 Genome-wide genotyping array 2017-02-19 27400856 Legge SE 2016-07-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27400856 Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia. Clozapine-induced agranulocytosis/granulocytopenia in treatment-resistant schizophrenia 48 European ancestry cases, 18 European ancestry extreme cases, 5,583 European ancestry controls 161 cases, 249 clozapine-exposed controls, 947 unexposed controls Illumina [7559010] (imputed) 10 Drug-induced agranulocytosis http://purl.obolibrary.org/obo/HP_0012235 GCST003628 Genome-wide genotyping array 2017-04-06 27883235 Martino DJ 2017-01-11 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/27883235 Genomewide association study of peanut allergy reproduces association with amino acid polymorphisms in HLA-DRB1. Peanut allergy 51 European ancestry infant cases, 14 Asian ancestry infant cases, 8 mixed European/Asian infant cases, 119 European ancestry non-allergic infant controls, 10 Asian ancestry non-allergic infant controls, 19 mixed European/Asian non-allergic infant controls 604 European ancestry infant cases, 34 mixed European/Asian infant cases, 2,871 European ancestry non-allergic infant controls, 40 mixed European/Asian non-allergic infant controls, 589 European ancestry infant controls, 1,148 European ancestry parent controls Illumina [3814967] (imputed) 0 peanut allergy measurement http://www.ebi.ac.uk/efo/EFO_0007017 GCST003881 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to selective serotonin reuptake inhibitors in depression 6,348 European ancestry responder cases, 3,340 European ancestry non-responder cases NA Illumina [~ 12000000] (imputed) 5 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST003801 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to citalopram or escitalopram in depression 2,963 European ancestry responder cases, 2,005 European ancestry non-responder cases NA Illumina [~ 12000000] (imputed) 7 response to escitalopram, response to citalopram http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329 GCST003802 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to antidepressants in depression 7,795 European ancestry responder cases, 1,311 European ancestry non-responder cases NA Illumina [~ 12000000] (imputed) 5 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST003803 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Non-response to bupropion and depression 1,861 European ancestry non-responder cases, 192,070 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 6 unipolar depression, response to bupropion, mood disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006326, http://www.ebi.ac.uk/efo/EFO_0004247 GCST003804 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to bupropion and depression 2,675 European ancestry responder cases, 191,986 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 5 unipolar depression, response to bupropion, mood disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006326, http://www.ebi.ac.uk/efo/EFO_0004247 GCST003806 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to selective serotonin reuptake inhibitors and depression 6,348 European ancestry responder cases, 191,357 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 5 unipolar depression, response to selective serotonin reuptake inhibitor, mood disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0004247 GCST003809 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Non-response to citalopram or escitalopram and depression 2,005 European ancestry non-responder cases, 192,083 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 5 unipolar depression, response to escitalopram, response to citalopram, mood disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329, http://www.ebi.ac.uk/efo/EFO_0004247 GCST003810 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to citalopram or escitalopram and depression 2,963 European ancestry responder cases, 191,936 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 5 unipolar depression, response to escitalopram, response to citalopram, mood disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329, http://www.ebi.ac.uk/efo/EFO_0004247 GCST003811 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Non-response to antidepressants and depression 1,311 European ancestry non-responder cases, 192,178 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 5 unipolar depression, mood disorder, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004247, http://purl.obolibrary.org/obo/GO_0036276 GCST003812 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Non-response to selective serotonin reuptake inhibitors and depression 3,340 European ancestry non-responder cases, 191,882 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 5 unipolar depression, response to selective serotonin reuptake inhibitor, mood disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0004247 GCST003808 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to antidepressants and depression 7,795 European ancestry responder cases, 191,173 European ancestry healthy controls NA Illumina [~ 12000000] (imputed) 5 unipolar depression, mood disorder, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004247, http://purl.obolibrary.org/obo/GO_0036276 GCST003813 Genome-wide genotyping array 2017-03-24 27622933 Li QS 2016-09-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/27622933 Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response. Response to bupropion in depression 2,675 European ancestry responder cases, 1,861 European ancestry non-responder cases NA Illumina [~ 12000000] (imputed) 5 response to bupropion http://www.ebi.ac.uk/efo/EFO_0006326 GCST003800 Genome-wide genotyping array 2017-04-05 27899403 Jones GT 2016-11-29 Circ Res www.ncbi.nlm.nih.gov/pubmed/27899403 Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci. Abdominal aortic aneurysm 4,972 European ancestry cases, 99,858 European ancestry controls 2,482 European ancestry cases, 2,750 cases, 2,645 European ancestry controls, 5,263 controls Affymetrix, Illumina [5363770] (imputed) 12 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST003877 Genome-wide genotyping array 2016-12-13 26993346 Schott JM 2016-03-15 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/26993346 Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease. Posterior cortical atrophy and Alzheimer's disease 293 cases, 10,547 healthy controls NA Illumina [~ 5900000] (imputed) 18 posterior cortical atrophy, Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0018899, http://purl.obolibrary.org/obo/MONDO_0004975 GCST003452 Genome-wide genotyping array 2017-04-21 27899376 Nakayama A 2016-11-29 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/27899376 GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes. Gout 945 Japanese ancestry cases, 1,213 Japanese ancestry controls 1,396 Japanese ancestry cases, 1,268 Japanese ancestry controls, 1,319 European ancestry cases, 514 European ancestry controls, 971 Polynesian ancestry cases, 565 Polynesian ancestry controls Illumina [570442] 11 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST003925 Genome-wide genotyping array 2017-04-21 27899376 Nakayama A 2016-11-29 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/27899376 GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes. Renal underexcretion gout 619 Japanese ancestry cases, 1,213 Japanese ancestry controls 696 Japanese ancestry cases, 1,268 Japanese ancestry controls Illumina [570442] 8 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST003926 Genome-wide genotyping array 2017-04-21 27899376 Nakayama A 2016-11-29 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/27899376 GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes. Renal overload gout 560 Japanese ancestry cases, 1,213 Japanese ancestry controls 618 Japanese ancestry cases, 1,268 Japanese ancestry controls Illumina [570442] 5 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST003924 Genome-wide genotyping array 2016-09-12 26377243 Li J 2015-09-17 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26377243 Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study. Lipoprotein (a) levels 2,895 African American individuals NA Affymetrix [up to 38000000] (imputed) 19 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST003127 Genome-wide genotyping array 2016-09-12 26394269 Cordell HJ 2015-09-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26394269 International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways. Primary biliary cholangitis 2,764 European ancestry cases, 10,475 European ancestry controls 3,716 European ancestry cases, 4,261 European ancestry controls Illumina [1143634] (imputed) 30 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST003129 Genome-wide genotyping array 2016-08-15 26366553 Danjou F 2015-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26366553 Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels. Hemoglobin levels 6,602 Sardinian founder individuals 4,131 European ancestry individuals Illumina [~ 10900000] (imputed) 8 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST003122 Genome-wide genotyping array 2016-05-12 26350878 Tashjian RZ 2015-09-05 J Shoulder Elbow Surg www.ncbi.nlm.nih.gov/pubmed/26350878 Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms. Rotator cuff tears 311 European ancestry cases, 2,641 European ancestry controls NA Illumina [257558] 2 rotator cuff tear http://www.ebi.ac.uk/efo/EFO_1001250 GCST003115 Genome-wide genotyping array 2016-10-14 26390057 Kato N 2015-09-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26390057 Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Systolic blood pressure 31,516 East Asian ancestry individuals, 35,352 European ancestry individuals, 33,126 South Asian ancestry individuals 87,205 individuals, 48,268 East Asian ancestry individuals, 68,456 European ancestry individuals and 16,328 South Asian ancestry individuals Affymetrix, Illumina, Perlegen [2127883] (imputed) 17 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST003272 Genome-wide genotyping array 2016-10-14 26390057 Kato N 2015-09-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26390057 Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Hypertension 31,516 East Asian ancestry individuals, 35,352 European ancestry individuals, 33,126 South Asian ancestry individuals 87,205 individuals, 48,268 East Asian ancestry individuals, 68,456 European ancestry individuals and 16,328 South Asian ancestry individuals Affymetrix, Illumina, Perlegen [~ 2100000] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST003276 Genome-wide genotyping array 2016-10-14 26390057 Kato N 2015-09-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26390057 Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Pulse pressure 31,516 East Asian ancestry individuals, 35,352 European ancestry individuals, 33,126 South Asian ancestry individuals 87,205 individuals, 48,268 East Asian ancestry individuals, 68,456 European ancestry individuals and 16,328 South Asian ancestry individuals Affymetrix, Illumina, Perlegen [~ 2100000] (imputed) 11 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST003274 Genome-wide genotyping array 2016-10-14 26390057 Kato N 2015-09-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26390057 Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Mean arterial pressure 31,516 East Asian ancestry individuals, 35,352 European ancestry individuals, 33,126 South Asian ancestry individuals 87,205 individuals, 48,268 East Asian ancestry individuals, 68,456 European ancestry individuals and 16,328 South Asian ancestry individuals Affymetrix, Illumina, Perlegen [~ 2100000] (imputed) 13 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST003275 Genome-wide genotyping array 2016-10-14 26390057 Kato N 2015-09-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26390057 Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Diastolic blood pressure 31,516 East Asian ancestry individuals, 35,352 European ancestry individuals, 33,126 South Asian ancestry individuals 87,205 individuals, 48,268 East Asian ancestry individuals, 68,456 European ancestry individuals, 16,328 South Asian ancestry individuals Affymetrix, Illumina, Perlegen [~ 2100000] (imputed) 20 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST003273 Genome-wide genotyping array 2016-06-13 26443449 Wang M 2015-10-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26443449 Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer. Prostate cancer 3,000 East Asian ancestry cases, 4,394 East Asian ancestry controls 3,605 East Asian ancestry cases, 3,919 East Asian ancestry controls Illumina [4550396] (imputed) 14 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST003148 Genome-wide genotyping array 2016-09-06 26343869 Xie G 2015-09-05 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/26343869 Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort. Carotid intima media thickness 810 Chinese ancestry individuals NA Illumina [32817] 12 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST003114 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Ear protrusion 4,919 Latin American individuals NA Illumina [671038] 3 ear protrusion http://www.ebi.ac.uk/efo/EFO_0007665 GCST002994 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Tragus size 4,919 Latin American individuals NA Illumina [671038] 1 tragus size http://www.ebi.ac.uk/efo/EFO_0007668 GCST003002 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Antitragus size 4,919 Latin American individuals NA Illumina [671038] 1 antitragus size http://www.ebi.ac.uk/efo/EFO_0007669 GCST003003 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Crus helix expression 4,919 Latin American individuals NA Illumina [671038] 0 crus helix expression http://www.ebi.ac.uk/efo/EFO_0007672 GCST003004 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Superior crus of antihelix expression 4,919 Latin American individuals NA Illumina [671038] 2 superior crus of antihelix expression http://www.ebi.ac.uk/efo/EFO_0007673 GCST003005 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Darwin's tubercle 4,919 Latin American individuals NA Illumina [671038] 0 Darwin's tubercule http://www.ebi.ac.uk/efo/EFO_0007674 GCST003000 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Ear morphology 4,919 Latin American individuals NA Illumina [671038] 7 outer ear morphology trait http://www.ebi.ac.uk/efo/EFO_0007664 GCST003001 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Lobe size 4,919 Latin American individuals NA Illumina [671038] 8 lobe size http://www.ebi.ac.uk/efo/EFO_0007666 GCST002999 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Lobe attachment 4,919 Latin American individuals NA Illumina [671038] 4 lobe attachment http://www.ebi.ac.uk/efo/EFO_0007667 GCST002998 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Helix rolling 4,919 Latin American individuals NA Illumina [671038] 6 helix rolling http://www.ebi.ac.uk/efo/EFO_0007670 GCST002997 Genome-wide genotyping array 2016-07-14 26105758 Adhikari K 2015-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26105758 A genome-wide association study identifies multiple loci for variation in human ear morphology. Folding of antihelix 4,919 Latin American individuals NA Illumina [671038] 5 folding of antihelix http://www.ebi.ac.uk/efo/EFO_0007671 GCST002996 Genome-wide genotyping array 2016-10-05 26561523 de Vries PS 2015-11-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26561523 A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. Fibrinogen levels 120,246 European ancestry individuals NA Affymetrix, Illumina [~ 10700000] (imputed) 41 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST003194 Genome-wide genotyping array 2016-09-28 26542096 Marenholz I 2015-11-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26542096 Meta-analysis identifies seven susceptibility loci involved in the atopic march. Atopic march 1,151 European ancestry early-onset eczema and childhood asthma cases, 10,030 European ancestry controls 1,277 European ancestry early-onset eczema and childhood asthma cases, 7,004 European ancestry controls Affymetrix, Illumina [1633153] (imputed) 7 atopic eczema, childhood onset asthma, atopic march http://www.ebi.ac.uk/efo/EFO_0000274, http://purl.obolibrary.org/obo/MONDO_0005405, http://www.ebi.ac.uk/efo/EFO_0007755 GCST003180 Genome-wide genotyping array 2016-09-30 26553974 McLaren PJ 2015-11-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/26553974 Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load. Setpoint viral load in HIV-1 infection 6,315 European ancestry cases NA Affymetrix, Illumina [~ 8000000] (imputed) 18 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST003183 Genome-wide genotyping array 2016-12-01 27015805 Pilling LC 2016-03-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/27015805 Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants. Parental longevity (father's age at death) 63,775 British middle-aged individuals 2,033 individuals Affymetrix [9678092] (imputed) 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST003392 Genome-wide genotyping array 2016-12-01 27015805 Pilling LC 2016-03-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/27015805 Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants. Parental longevity (mother's age at death) 52,776 middle-aged British individuals NA Affymetrix [9658292] (imputed) 51 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST003393 Genome-wide genotyping array 2016-12-01 27015805 Pilling LC 2016-03-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/27015805 Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants. Parental longevity (combined parental age at death) 45,627 middle-aged British individuals NA Affymetrix [9658292] (imputed) 51 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST003394 Genome-wide genotyping array 2016-12-01 27015805 Pilling LC 2016-03-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/27015805 Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants. Parental extreme longevity (95 years and older) 1,339 middle-aged British cases, 40,934 middle-aged British controls NA Affymetrix [9658292] (imputed) 73 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST003395 Genome-wide genotyping array 2016-12-20 27002377 Irvin MR 2016-07-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27002377 A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies. Response to fenofibrate (HDL cholesterol levels) 1,594 European ancestry individuals 350 Hispanic individuals, 138 African American individuals Affymetrix [6982258] (imputed) 15 HDL cholesterol change measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007805, http://purl.obolibrary.org/obo/GO_1901557 GCST003485 Genome-wide genotyping array 2016-12-20 27002377 Irvin MR 2016-07-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27002377 A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies. Response to fenofibrate (LDL cholesterol levels) 1,594 European ancestry individuals 350 Hispanic individuals, 138 African American individuals Affymetrix [6982258] (imputed) 12 LDL cholesterol change measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007804, http://purl.obolibrary.org/obo/GO_1901557 GCST003486 Genome-wide genotyping array 2016-12-20 27002377 Irvin MR 2016-07-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27002377 A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies. Response to fenofibrate (total cholesterol levels) 1,594 European ancestry individuals 350 Hispanic individuals, 138 African American individuals Affymetrix [6982258] (imputed) 18 total cholesterol change measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007806, http://purl.obolibrary.org/obo/GO_1901557 GCST003487 Genome-wide genotyping array 2016-12-20 27002377 Irvin MR 2016-07-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27002377 A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies. Response to fenofibrate (triglyceride levels) 1,594 European ancestry individuals 350 Hispanic individuals, 138 African American individuals Affymetrix [6982258] (imputed) 17 triglyceride change measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007681, http://purl.obolibrary.org/obo/GO_1901557 GCST003488 Genome-wide genotyping array 2016-04-12 26629533 Meng W 2015-08-04 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/26629533 A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain. Neuropathic pain in type 2 diabetes 470 European ancestry male cases, 491 European ancestry female cases, 2,021 European ancestry male controls, 1,239 European ancestry female controls NA Affymetrix, Illumina [6906962] (imputed) 3 neuropathic pain http://www.ebi.ac.uk/efo/EFO_0005762 GCST003063 Genome-wide genotyping array 2016-12-16 27021288 Brevik EJ 2016-03-29 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/27021288 Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder. Aggressiveness in attention deficit hyperactivity disorder 1,060 European ancestry adult cases NA Illumina [7576458] (imputed) 32 aggressive behaviour measurement, childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007826, http://www.ebi.ac.uk/efo/EFO_0007663 GCST003473 Genome-wide genotyping array 2016-12-16 27021288 Brevik EJ 2016-03-29 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/27021288 Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder. Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder 750 European ancestry child cases NA Illumina [1871025] (imputed) 24 oppositional defiant disorder measurement http://www.ebi.ac.uk/efo/EFO_0007679 GCST003472 Genome-wide genotyping array 2016-12-07 27005825 Finkel TH 2016-03-22 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/27005825 Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility. Arthritis (juvenile idiopathic) 388 European ancestry cases, 2,500 European ancestry controls 778 European ancestry cases, 7,000 European ancestry controls Illumina [at least 518907] (imputed) 1 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST003424 Genome-wide genotyping array 2017-02-10 27339598 Ulveling D 2016-07-29 Hepatology www.ncbi.nlm.nih.gov/pubmed/27339598 A new 3p25 locus is associated with liver fibrosis progression in human immunodeficiency virus/hepatitis C virus-coinfected patients. Liver fibrosis severity in HIV/hepatitis C co-infection 289 French ancestry cases NA Illumina [8426597] (imputed) 7 Hepatic fibrosis http://purl.obolibrary.org/obo/HP_0001395 GCST003606 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Subcutaneous adipose tissue 7,399 European ancestry women, 7,381 European ancestry men, 2,163 African American women, 1,304 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 1 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST003965 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue 7,431 European ancestry women, 7,432 European ancestry men, 2,163 African American women, 1,306 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST003966 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Pericardial adipose tissue adjusted for height and weight 3,684 European ancestry women, 3,640 European ancestry men, 1,284 African American women, 877 African American men, 746 Hispanic Ancestry women, 699 Hispanic ancestry men, 390 Asian ancestry women, 378 Asian ancestry men, 294 Old Order Amish (founder/genetic isolate) women, 248 Old Order Amish (founder/genetic isolate) men. NA Affymetrix, Illumina [~ 2600000] (imputed) 5 pericardial adipose tissue measurement, body weight, body height http://www.ebi.ac.uk/efo/EFO_0007890, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004339 GCST003968 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue adjusted for BMI 7,431 European ancestry women, 7,432 European ancestry men, 2,163 African American women, 1,306 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 2 visceral adipose tissue measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004765, http://www.ebi.ac.uk/efo/EFO_0004340 GCST003967 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Pericardial fat 3,684 European ancestry women, 3,640 European ancestry men, 1,284 African American women, 877 African American men, 746 Hispanic Ancestry women, 699 Hispanic ancestry men, 390 Asian ancestry women, 378 Asian ancestry men, 294 Old Order Amish (founder/genetic isolate) women, 248 Old Order Amish (founder/genetic isolate) men. NA Affymetrix, Illumina [~ 2600000] (imputed) 2 pericardial adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0007890 GCST003971 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Subcutaneous adipose tissue attenuation (Hounsfield unit scale) 5,699 European ancestry women, 5,699 European ancestry men, 592 African American women, 449 African American men. NA Affymetrix, Illumina [~ 2600000] (imputed) 0 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST003970 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue attenuation (Hounslow unit scale) 5,729 European ancestry women, 5,749 European ancestry men, 592 African American women, 449 African American men. NA Affymetrix, Illumina [~ 2600000] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST003969 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue/subcutaneous adipose tissue ratio 7,618 European ancestry women, 7,050 European ancestry men, 2,205 African American women, 1,324 African American men. NA Affymetrix, Illumina [~ 2600000] (imputed) 4 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST003972 Genome-wide genotyping array 2017-05-11 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue/subcutaneous adipose tissue ratio adjusted for BMI 7,618 European ancestry women, 7,050 European ancestry men, 2,205 African American women, 1,324 African American men. NA Affymetrix, Illumina [~ 2600000] (imputed) 4 body mass index, visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004767 GCST003973 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue adjusted for BMI 7,432 European ancestry men, 1,306 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 1 visceral adipose tissue measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004765, http://www.ebi.ac.uk/efo/EFO_0004340 GCST006534 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue adjusted for BMI 7,431 European ancestry women, 2,163 African American women NA Affymetrix, Illumina [~ 2600000] (imputed) 2 visceral adipose tissue measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004765, http://www.ebi.ac.uk/efo/EFO_0004340 GCST006533 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Subcutaneous adipose tissue 7,399 European ancestry women, 2,163 African American women NA Affymetrix, Illumina [~ 2600000] (imputed) 1 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST006537 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Subcutaneous adipose tissue 7,381 European ancestry men, 1,304 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 0 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST006538 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue 7,432 European ancestry men, 1,306 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST006540 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue 7,431 European ancestry women, 2,163 African American women NA Affymetrix, Illumina [~ 2600000] (imputed) 1 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST006542 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Pericardial adipose tissue adjusted for height and weight 3,640 European ancestry men, 877 African American men, 699 Hispanic ancestry men, 378 Asian ancestry men, 248 Old Order Amish (founder/genetic isolate) men. NA Affymetrix, Illumina [~ 2600000] (imputed) 1 pericardial adipose tissue measurement, body weight, body height http://www.ebi.ac.uk/efo/EFO_0007890, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004339 GCST006543 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Pericardial adipose tissue adjusted for height and weight 3,684 European ancestry women, 1,284 African American women, 746 Hispanic Ancestry women, 390 Asian ancestry women, 294 Old Order Amish (founder/genetic isolate) women NA Affymetrix, Illumina [~ 2600000] (imputed) 3 pericardial adipose tissue measurement, body weight, body height http://www.ebi.ac.uk/efo/EFO_0007890, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004339 GCST006544 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Subcutaneous adipose tissue attenuation (Hounsfield unit scale) 5,699 European ancestry women, 592 African American women NA Affymetrix, Illumina [~ 2600000] (imputed) 0 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST006550 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Subcutaneous adipose tissue attenuation (Hounsfield unit scale) 5,699 European ancestry men, 449 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 2 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST006549 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Pericardial fat 3,640 European ancestry men, 877 African American men, 699 Hispanic ancestry men, 378 Asian ancestry men, 248 Old Order Amish (founder/genetic isolate) men NA Affymetrix, Illumina [~ 2600000] (imputed) 0 pericardial adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0007890 GCST006545 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Pericardial fat 3,684 European ancestry women, 1,284 African American women, 746 Hispanic Ancestry women, 390 Asian ancestry women, 294 Old Order Amish (founder/genetic isolate) women NA Affymetrix, Illumina [~ 2600000] (imputed) 0 pericardial adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0007890 GCST006546 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue attenuation (Hounslow unit scale) 5,749 European ancestry men, 449 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 1 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST006547 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue attenuation (Hounslow unit scale) 5,729 European ancestry women, 592 African American women NA Affymetrix, Illumina [~ 2600000] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST006548 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue/subcutaneous adipose tissue ratio 7,050 European ancestry men, 1,324 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 0 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST006552 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue/subcutaneous adipose tissue ratio 7,618 European ancestry women, 2,205 African American women NA Affymetrix, Illumina [~ 2600000] (imputed) 0 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST006551 Genome-wide genotyping array 2017-02-27 27490719 Bacelis J 2016-08-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/27490719 Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. Gestational age at birth (maternal effect) 1,743 Norwegian ancestry mothers NA NR [525577] 2 gestational age, birth measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0006921 GCST003688 Genome-wide genotyping array 2017-02-27 27490719 Bacelis J 2016-08-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/27490719 Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. Gestational age at birth in labor-initiated deliveries (child effect) 884 Norwegian ancestry children NA NR [525577] 12 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST003687 Genome-wide genotyping array 2017-02-27 27490719 Bacelis J 2016-08-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/27490719 Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. Gestational age at birth in premature rupture of membrane-initiated deliveries (child effect) 225 Norwegian ancestry children NA NR [525577] 8 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST003689 Genome-wide genotyping array 2017-02-27 27490719 Bacelis J 2016-08-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/27490719 Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. Gestational age at birth in labor-initiated deliveries (maternal effect) 1,407 Norwegian ancestry mothers NA NR [525577] 2 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST003684 Genome-wide genotyping array 2017-02-27 27490719 Bacelis J 2016-08-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/27490719 Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. Gestational age at birth in premature rupture of membrane-initiated deliveries (maternal effect) 336 Norwegian ancestry mothers NA NR [525577] 8 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST003685 Genome-wide genotyping array 2017-02-27 27490719 Bacelis J 2016-08-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/27490719 Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways. Gestational age at birth (child effect) 1,109 Norwegian ancestry children NA NR [525577] 13 gestational age, birth measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0006921 GCST003686 Genome-wide genotyping array 2017-05-12 27918536 Lo MT 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918536 Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders. Agreeableness 76,551 European ancestry individuals NA Affymetrix, Illumina [2165398] (imputed) 0 agreeableness measurement http://www.ebi.ac.uk/efo/EFO_0007915 GCST004013 Genome-wide genotyping array 2017-05-12 27918536 Lo MT 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918536 Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders. Conscientiousness 76,551 European ancestry individuals 46,581 European ancestry individuals Affymetrix, Illumina [2166809] (imputed) 1 conscientiousness measurement http://www.ebi.ac.uk/efo/EFO_0007912 GCST004014 Genome-wide genotyping array 2017-05-12 27918536 Lo MT 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918536 Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders. Extraversion 122,886 European ancestry individuals 46,621 European ancestry individuals Affymetrix, Illumina [6343667] (imputed) 5 extraversion http://www.ebi.ac.uk/efo/EFO_0004317 GCST004015 Genome-wide genotyping array 2017-05-12 27918536 Lo MT 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918536 Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders. Neuroticism 122,867 European ancestry individuals 137,994 European ancestry individuals Affymetrix, Illumina [6337541] (imputed) 2 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST004017 Genome-wide genotyping array 2017-05-12 27918536 Lo MT 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918536 Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders. Openness 76,581 European ancestry individuals NA Affymetrix, Illumina [2167320] (imputed) 0 openness measurement http://www.ebi.ac.uk/efo/EFO_0007914 GCST004016 Genome-wide genotyping array 2017-06-19 28319091 Styrkarsdottir U 2017-03-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28319091 Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis. Osteoarthritis (with total hip replacement) 3,110 Icelandic ancestry cases, 1,547 non-array typed, familial imputed Icelandic ancestry cases, 99,911 Icelandic ancestry controls, 107,603 non-array typed, familial imputed Icelandic ancestry controls NA Illumina [up to 31600000] (imputed) 2 hip osteoarthritis symptom severity measurement, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0007942, http://purl.obolibrary.org/obo/MONDO_0005178 GCST004199 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue/subcutaneous adipose tissue ratio adjusted for BMI 7,618 European ancestry women, 2,205 African American women NA Affymetrix, Illumina [~ 2600000] (imputed) 0 body mass index, visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004767 GCST006553 Genome-wide genotyping array 2018-11-09 27918534 Chu AY 2016-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27918534 Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation. Visceral adipose tissue/subcutaneous adipose tissue ratio adjusted for BMI 7,050 European ancestry men, 1,324 African American men NA Affymetrix, Illumina [~ 2600000] (imputed) 0 body mass index, visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004767 GCST006554 Genome-wide genotyping array 2017-01-27 27386562 Andlauer TF 2016-06-17 Sci Adv www.ncbi.nlm.nih.gov/pubmed/27386562 Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Multiple sclerosis 4,888 German ancestry cases, 10,395 German ancestry controls 2,903 Sardinian ancestry cases, 3,323 Sardinian ancestry controls Illumina [at least 8143088] (imputed) 16 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST003566 Genome-wide genotyping array 2016-11-18 26819262 Zhou Y 2016-01-27 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26819262 Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis. Epstein Barr virus nuclear antigen 1 IgG levels 1,243 parents and up to 2,356 children from 992 families, 1,956 Mexican American individuals Illumina [up to 2428201] (imputed) 9 Epstein Barr virus nuclear antigen 1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0007790 GCST003339 Genome-wide genotyping array 2016-11-18 26819262 Zhou Y 2016-01-27 Mult Scler www.ncbi.nlm.nih.gov/pubmed/26819262 Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis. Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis 3,599 individuals, 1,956 Mexican American individuals, 5,545 European ancestry multiple sclerosis cases, 12,153 European ancestry non-multiple sclerosis controls Illumina [up to 2529394] (imputed) 4 Epstein Barr virus nuclear antigen 1 IgG measurement, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0007790, http://purl.obolibrary.org/obo/MONDO_0005301 GCST003340 Genome-wide genotyping array 2016-11-14 26818729 Weinsheimer S 2016-01-27 J Neurol Neurosurg Psychiatry www.ncbi.nlm.nih.gov/pubmed/26818729 Genome-wide association study of sporadic brain arteriovenous malformations. Brain arteriovenous malformations (sporadic) 515 European ancestry cases, 1191 European ancestry controls 608 European ancestry cases, 744 European ancestry controls Affymetrix [4300568] (imputed) 0 Cerebral arteriovenous malformation http://www.orpha.net/ORDO/Orphanet_46724 GCST003318 Genome-wide genotyping array 2016-10-06 26686553 Jorgenson E 2015-12-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26686553 A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia. Inguinal hernia 5,295 European ancestry cases, 67,510 European ancestry controls 9,701 European ancestry cases, 82,743 European ancestry controls Affymetrix [6161781] (imputed) 4 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST003198 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebral amyloid deposition (PET imaging) up to 883 European and other ancestry individuals NA Illumina [~ 9000000] (imputed) 17 cerebral amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0007707 GCST003073 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebrospinal fluid AB1-42 levels up to 189 European and other ancestry early mild cognitive impairment cases, up to 251 European and other ancestry late mild cognitive impairment cases, up to 121 European and other ancestry Alzheimer's disease cases, up to 215 European and other ancestry healthy controls up to 3 European and other ancestry significant memory concern cases, up to 57 European and other ancestry early mild cognitive impairment cases, up to 61 European and other ancestry late mild cognitive impairment cases, up to 62 European and other ancestry Alzheimer's disease cases, up to 21 European and other ancestry healthy controls Illumina [~ 9000000] (imputed) 8 beta-amyloid 1-42 measurement, cerebrospinal fluid biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004670, http://www.ebi.ac.uk/efo/EFO_0006794 GCST003072 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cognitive decline rate in late mild cognitive impairment 472 European ancestry cases, 47 cases NA Illumina [~ 9000000] (imputed) 143 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST003075 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebral amyloid deposition in APOEe4 non-carriers (PET imaging) 370 European and other ancestry APOEe4 non-carriers NA Illumina [~ 9000000] (imputed) 26 cerebral amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0007707 GCST003074 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebrospinal T-tau levels up to 189 European and other ancestry early mild cognitive impairment cases, up to 251 European and other ancestry late mild cognitive impairment cases, up to 121 European and other ancestry Alzheimer's disease cases, up to 215 European and other ancestry healthy controls up to 3 European and other ancestry significant memory concern cases, up to 57 European and other ancestry early mild cognitive impairment cases, up to 61 European and other ancestry late mild cognitive impairment cases, up to 62 European and other ancestry Alzheimer's disease cases, up to 21 European and other ancestry healthy controls Illumina [~ 9000000] (imputed) 6 cerebrospinal fluid biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006794, http://www.ebi.ac.uk/efo/EFO_0004760 GCST003070 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebrospinal P-tau181p levels up to 189 European and other ancestry early mild cognitive impairment cases, up to 251 European and other ancestry late mild cognitive impairment cases, up to 121 European and other ancestry Alzheimer's disease cases, up to 215 European and other ancestry healthy controls up to 3 European and other ancestry significant memory concern cases, up to 57 European and other ancestry early mild cognitive impairment cases, up to 61 European and other ancestry late mild cognitive impairment cases, up to 62 European and other ancestry Alzheimer's disease cases, up to 21 European and other ancestry healthy controls Illumina [~ 9000000] (imputed) 4 p-tau measurement, cerebrospinal fluid biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006794 GCST003071 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebrospinal fluid p-Tau181p:AB1-42 ratio up to 189 European and other ancestry early mild cognitive impairment cases, up to 251 European and other ancestry late mild cognitive impairment cases, up to 121 European and other ancestry Alzheimer's disease cases, up to 215 European and other ancestry healthy controls up to 3 European and other ancestry significant memory concern cases, up to 57 European and other ancestry early mild cognitive impairment cases, up to 61 European and other ancestry late mild cognitive impairment cases, up to 62 European and other ancestry Alzheimer's disease cases, up to 21 European and other ancestry healthy controls Illumina [~ 9000000] (imputed) 4 p-tau:beta-amyloid 1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0007709 GCST003078 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebrospinal fluid t-tau:AB1-42 ratio up to 189 European and other ancestry early mild cognitive impairment cases, up to 251 European and other ancestry late mild cognitive impairment cases, up to 121 European and other ancestry Alzheimer's disease cases, up to 215 European and other ancestry health up to 3 European and other ancestry significant memory concern cases, up to 57 European and other ancestry early mild cognitive impairment cases, up to 61 European and other ancestry late mild cognitive impairment cases, up to 62 European and other ancestry Alzheimer's disease cases, up to 21 European and other ancestry healthy controls Illumina [~ 9000000] (imputed) 6 t-tau:beta-amyloid 1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0007708 GCST003079 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebral amyloid deposition in APOEe4 carriers (PET imaging) 263 European and other ancestry APOEe4 carriers NA Illumina [~ 9000000] (imputed) 0 cerebral amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0007707 GCST003076 Genome-wide genotyping array 2016-09-08 26252872 Li QS 2015-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26252872 Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid Aβ1-42 Level. Cerebral amyloid deposition positivity (PET imaging) up to 350 European and other ancestry positive individuals, up to 296 European and other ancestry negative individuals NA Illumina [~ 9000000] (imputed) 1 cerebral amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0007707 GCST003077 Genome-wide genotyping array 2016-11-21 26822151 Hartiala JA 2016-01-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26822151 Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease. Betaine levels in individuals undergoing cardiac evaluation 1,985 individuals 1,895 individuals Affymetrix [2421770] (imputed) 2 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST003358 Genome-wide genotyping array 2016-12-08 26830138 Herold C 2016-02-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26830138 Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3. Alzheimer disease and age of onset 2,478 European ancestry cases, 979 ancestry controls both from the same 1,070 families NA Affymetrix [up to 15107142] (imputed) 203 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST003427 Genome-wide genotyping array 2016-12-08 26959717 Nicoletti P 2016-03-09 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/26959717 HLA-DRB1*16: 01-DQB1*05: 02 is a novel genetic risk factor for flupirtine-induced liver injury. Drug-induced liver injury 620 European ancestry cases, 10,588 European ancestry controls NA Illumina [NR] (imputed) 1 response to flupirtine, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007809, http://www.ebi.ac.uk/efo/EFO_0004228 GCST003426 Genome-wide genotyping array 2016-10-04 26600424 MacInnis MJ 2015-11-24 High Alt Med Biol www.ncbi.nlm.nih.gov/pubmed/26600424 A Preliminary Genome-Wide Association Study of Acute Mountain Sickness Susceptibility in a Group of Nepalese Pilgrims Ascending to 4380 m. Acute mountain sickness 43 Nepalese cases, 56 Nepalese controls 102 Nepalese cases, 100 Nepalese controls Illumina [270389] 0 altitude sickness http://www.ebi.ac.uk/efo/EFO_1000782 GCST003188 Genome-wide genotyping array 2016-12-14 26833182 Ware JJ 2016-02-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26833182 Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2. Cotinine levels in current smokers up to 4,548 European ancestry daily smoker individuals 755 European ancestry daily smoker individuals Affymetrix, Illumina, Perlegen [up to 8585905] (imputed) 0 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST003466 Genome-wide genotyping array 2016-10-06 26621817 Cheng TH 2015-12-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26621817 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. Colorectal or endometrial cancer 5,725 European ancestry colorectal carcinoma cases, 2,212 European ancestry endometrial carcinoma cases, 13,396 European ancestry controls NA Illumina [up to 6000000] (imputed) 16 colorectal cancer, endometrial neoplasm http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0004230 GCST003209 Genome-wide genotyping array 2016-10-06 26621817 Cheng TH 2015-12-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26621817 Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1. Colorectal or endometrial cancer 5,725 European ancestry colorectal carcinoma cases, 2,212 European ancestry endometrial carcinoma cases, 13,396 European ancestry controls 4,330 European ancestry endometrial carcinoma cases, 26,849 European ancestry controls Illumina [up to 6000000] (imputed) 13 colorectal cancer, endometrial neoplasm http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0004230 GCST003208 Genome-wide genotyping array 2016-07-29 26272126 Oddsson A 2015-08-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26272126 Common and rare variants associated with kidney stones and biochemical traits. Kidney stones 5,149 European ancestry cases, 279,870 European ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [28300000] (imputed) 4 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST003086 Genome-wide genotyping array 2016-04-23 26041818 Chesi A 2015-06-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26041818 A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius. Pediatric areal bone mineral density (radius) 178 African American females, 159 African American males, 474 European ancestry females, 434 European ancestry males, 54 Hispanic and other ancestry females, 72 Hispanic and other ancestry males 242 European ancestry females, 239 European ancestry males Illumina [7238679] (imputed) 2 radius bone mineral density http://www.ebi.ac.uk/efo/EFO_0007933 GCST002953 Genome-wide genotyping array 2016-04-23 26041818 Chesi A 2015-06-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26041818 A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius. Pediatric bone mineral content (radius) 178 African American females, 159 African American males, 474 European ancestry females, 434 European ancestry males, 54 Hispanic and other ancestry females, 72 Hispanic and other ancestry males 242 European ancestry females, 239 European ancestry males Illumina [7238679] (imputed) 3 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST002952 Genome-wide genotyping array 2016-09-12 26420894 Wuttke M 2015-09-28 Nephrol Dial Transplant www.ncbi.nlm.nih.gov/pubmed/26420894 Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium. Proteinuria in chronic kidney disease up to 744 European ancestry child cases, up to 397 Turkish ancestry child cases NA Illumina [~ 8300000] (imputed) 4 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST003142 Genome-wide genotyping array 2016-09-12 26420894 Wuttke M 2015-09-28 Nephrol Dial Transplant www.ncbi.nlm.nih.gov/pubmed/26420894 Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium. Chronic kidney disease 658 European ancestry child cases, 1,347 European ancestry child controls NA Illumina [~ 8300000] (imputed) 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST003140 Genome-wide genotyping array 2016-09-12 26420894 Wuttke M 2015-09-28 Nephrol Dial Transplant www.ncbi.nlm.nih.gov/pubmed/26420894 Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium. Proteinuria and chronic kidney disease 294 European ancestry child cases, 1,347 European ancestry child controls NA Illumina [~ 10500000] (imputed) 9 chronic kidney disease, Proteinuria http://www.ebi.ac.uk/efo/EFO_0003884, http://purl.obolibrary.org/obo/HP_0000093 GCST003141 Genome-wide genotyping array 2016-09-12 26420894 Wuttke M 2015-09-28 Nephrol Dial Transplant www.ncbi.nlm.nih.gov/pubmed/26420894 Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium. Glomerular filtration rate in chronic kidney disease up to 744 Central European ancestry child cases, up to 397 Turkish ancestry child cases NA Illumina [~ 8300000] (imputed) 22 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST003139 Genome-wide genotyping array 2016-06-16 26268530 Ramanan VK 2015-08-11 Brain www.ncbi.nlm.nih.gov/pubmed/26268530 GWAS of longitudinal amyloid accumulation on 18F-florbetapir PET in Alzheimer's disease implicates microglial activation gene IL1RAP. Longitudinal change in brain amyloid plaque burden 41 European ancestry Alzheimer's disease cases, 294 European ancestry Mild Cognitive Impairment cases, 160 European ancestry cognitively normal individuals NA Illumina [6112217] (imputed) 9 amyloid plaque accumulation rate http://www.ebi.ac.uk/efo/EFO_0007646 GCST003082 Genome-wide genotyping array 2016-07-15 26034056 Hoffmann TJ 2015-06-01 Cancer Discov www.ncbi.nlm.nih.gov/pubmed/26034056 A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences. Prostate cancer 6,406 European ancestry cases, 601 African American cases, 288 East Asian ancestry cases, 488 Latino cases30,866 European ancestry controls, 1,650 African American controls, 2,938 East Asian ancestry controls, 3,141 Latino controls 4,599 European ancestry cases, 2,265 African American cases, 2,940 European ancestry controls, 2,414 African American controls Affymetrix [up to 19977088] (imputed) 57 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002944 Genome-wide genotyping array 2016-04-26 26039976 Wei Z 2015-06-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26039976 Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations. HIV-1 viral setpoint 326 Han Chinese ancestry cases, 58 Dai Chinese ancestry cases, 40 Jingpo Chinese ancestry cases, 83 Uygur Chinese ancestry cases, 11 Hui Chinese ancestry cases, 20 East Asian cases NA Illumina [up to 528294] 9 HIV viral set point measurement http://www.ebi.ac.uk/efo/EFO_0006319 GCST002976 Genome-wide genotyping array 2016-09-27 26580837 Chen CJ 2015-11-18 Biomark Med www.ncbi.nlm.nih.gov/pubmed/26580837 A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population. Amyotrophic lateral sclerosis 94 Taiwanese Han ancestry cases, 376 Taiwanese Han ancestry controls NA Affymetrix [633420] 6 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST003175 Genome-wide genotyping array 2016-08-17 26233692 Gan-Or Z 2015-08-02 J Neurol www.ncbi.nlm.nih.gov/pubmed/26233692 The Alzheimer disease BIN1 locus as a modifier of GBA-associated Parkinson disease. Parkinson's disease in GBA mutation carriers (age at onset) 79 Ashkenazi Jewish (founder/genetic isolate) GBA mutation carriers 34 Ashkenazi Jewish (founder/genetic isolate) mild GBA mutation carriers, 41 Ashkenazi Jewish (founder/genetic isolate) severe GBA mutation carriers Affymetrix [NR] 0 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST003060 Genome-wide genotyping array 2016-10-13 26674333 Traylor M 2015-12-16 Neurology www.ncbi.nlm.nih.gov/pubmed/26674333 Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke. White matter hyperintensities in ischemic stroke 3,670 European ancestry cases NA Affymetrix, Illumina [7567914] (imputed) 8 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST003245 Genome-wide genotyping array 2016-11-09 26908625 Johansson A 2016-01-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26908625 Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome. NT-proBNP levels in acute coronary syndrome at least 3,691 European ancestry individuals, up to 29 Asian ancestry individuals, 20 African ancestry individuals at least 5,404 European ancestry individuals, up to 54 Asian ancestry individuals, 33 African ancestry individuals Illumina [10962468] (imputed) 3 cardiovascular disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005278 GCST003298 Genome-wide genotyping array 2016-11-18 26732621 Ruth KS 2016-01-04 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/26732621 Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health. Length of menstrual cycle 9,534 European ancestry individuals NA NR [~ 16800000] (imputed) 2 menstrual cycle measurement http://www.ebi.ac.uk/efo/EFO_0007786 GCST003334 Genome-wide genotyping array 2016-11-25 26754954 Otowa T 2016-01-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26754954 Meta-analysis of genome-wide association studies of anxiety disorders. Anxiety disorder up to 7,016 European ancestry cases, up to 14,745 European ancestry controls NA Affymetrix, Illumina, Perlegen [~ 6500000] (imputed) 1 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST003370 Genome-wide genotyping array 2016-11-25 26754954 Otowa T 2016-01-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26754954 Meta-analysis of genome-wide association studies of anxiety disorders. Anxiety disorder (factor score) 18,186 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 6500000] (imputed) 1 anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0007795 GCST003369 Genome-wide genotyping array 2016-11-24 26752167 Taylor JY 2016-01-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26752167 A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction. Systolic blood pressure (cigarette smoking interaction) 1,083 African American individuals 1,427 African American individuals Affymetrix [761050] 8 systolic blood pressure, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005671 GCST003365 Genome-wide genotyping array 2016-11-24 26752167 Taylor JY 2016-01-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26752167 A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction. Diastolic blood pressure (cigarette smoking interaction) 1,083 African American individuals 1,427 African American individuals Affymetrix [761050] 0 diastolic blood pressure, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005671 GCST003366 Genome-wide genotyping array 2016-11-18 26746183 Watanabe H 2016-01-08 J Neurol Neurosurg Psychiatry www.ncbi.nlm.nih.gov/pubmed/26746183 A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN. Rapid functional decline in sporadic amyotrophic lateral sclerosis 59 Japanese ancestry cases with rapid functional decline, 110 Japanese ancestry cases with intermediate functional decline, 70 Japanese ancestry cases with sigmoidal functional decline, 215 Japanese ancestry cases with moderate functional decline NA Illumina [572983] 1 functional decline measurement http://www.ebi.ac.uk/efo/EFO_0007784 GCST003332 Genome-wide genotyping array 2016-11-18 26746183 Watanabe H 2016-01-08 J Neurol Neurosurg Psychiatry www.ncbi.nlm.nih.gov/pubmed/26746183 A rapid functional decline type of amyotrophic lateral sclerosis is linked to low expression of TTN. Moderate functional decline in sporadic amyotrophic lateral sclerosis 215 Japanese ancestry cases with moderate functional decline, 59 Japanese ancestry cases with rapid functional decline, 110 Japanese ancestry cases with intermediate functional decline, 70 Japanese ancestry cases with sigmoidal functional decline NA Illumina [572983] 0 functional decline measurement http://www.ebi.ac.uk/efo/EFO_0007784 GCST003333 Genome-wide genotyping array 2016-10-05 26704534 Sapkota BR 2015-12-15 J Steroid Biochem Mol Biol www.ncbi.nlm.nih.gov/pubmed/26704534 Genome-wide association study of 25(OH) Vitamin D concentrations in Punjabi Sikhs: Results of the Asian Indian diabetic heart study. Vitamin D levels 1,387 Punjabi Sikh ancestry individuals 2,151 Punjabi Sikh ancestry individuals Illumina [5904251] (imputed) 2 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST003191 Genome-wide genotyping array 2016-11-17 26776603 Honne K 2016-01-18 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/26776603 A longitudinal genome-wide association study of anti-tumor necrosis factor response among Japanese patients with rheumatoid arthritis. Response to anti-TNF therapy in rheumatoid arthritis 31 Japanese ancestry mild cases, 282 Japanese ancestry moderate cases, 131 Japanese ancestry severe cases NA Illumina [4253138] (imputed) 12 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST003329 Genome-wide genotyping array 2016-12-01 26831199 Pattaro C 2016-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26831199 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Glomerular filtration rate in non diabetics (creatinine) 118,448 European ancestry individuals 36,433 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 37 creatinine measurement, glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0005208 GCST003401 Genome-wide genotyping array 2016-11-25 26831199 Pattaro C 2016-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26831199 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Glomerular filtration rate in diabetics (creatinine) 11,522 European ancestry individuals 4,955 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 1 creatinine measurement, glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0005208 GCST003373 Genome-wide genotyping array 2016-11-25 26831199 Pattaro C 2016-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26831199 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Glomerular filtration rate (cystatin C) 32,834 European ancestry individuals 14,930 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 1 glomerular filtration rate, cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0004617 GCST003375 Genome-wide genotyping array 2016-11-25 26831199 Pattaro C 2016-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26831199 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Chronic kidney disease 12,385 European ancestry cases, 104,780 European ancestry controls 33,972 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 10 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST003374 Genome-wide genotyping array 2016-11-25 26831199 Pattaro C 2016-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26831199 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Glomerular filtration rate (creatinine) 133,413 European ancestry individuals 42,166 European ancestry individuals, up to 16,471 African ancestry individuals, up to 42,296 Asian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 63 creatinine measurement, glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0005208 GCST003372 Genome-wide genotyping array 2016-11-25 26831199 Pattaro C 2016-01-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26831199 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Glomerular filtration rate (creatinine) 133,413 European ancestry individuals, 16,840 African ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 0 creatinine measurement, glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0005208 GCST003371 Genome-wide genotyping array 2016-12-14 26824906 Rankinen T 2016-01-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/26824906 No Evidence of a Common DNA Variant Profile Specific to World Class Endurance Athletes. World class endurance athleticism 60 Japanese ancestry world-class cases, 116 Japanese ancestry controls at least 140 Sub-Saharan African ancestry cases, at least 275 Sub-Saharan African ancestry controls, at least 606 European ancestry cases, at least 978 European ancestry controls, at least 688 Japanese ancestry controls, 78 cases, 101 controls. Illumina [541179] 3 athletic endurance measurement http://www.ebi.ac.uk/efo/EFO_0007818 GCST003458 Genome-wide genotyping array 2016-12-14 26824906 Rankinen T 2016-01-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/26824906 No Evidence of a Common DNA Variant Profile Specific to World Class Endurance Athletes. Endurance athleticism 60 Japanese ancestry world-class cases, 116 Japanese ancestry controls at least 343 Sub-Saharan African ancestry cases, at least 275 Sub-Saharan African ancestry controls, at least 837 European ancestry cases, at least 978 European ancestry controls, at least 137 Japanese ancestry cases, at least 688 Japanese ancestry controls, 78 cases, 101 controls. Illumina [541179] 0 athletic endurance measurement http://www.ebi.ac.uk/efo/EFO_0007818 GCST003459 Genome-wide genotyping array 2016-11-18 26821981 Koga AT 2016-01-28 J Neural Transm (Vienna) www.ncbi.nlm.nih.gov/pubmed/26821981 Genome-wide association analysis to predict optimal antipsychotic dosage in schizophrenia: a pilot study. antipsychotic drug dosage in schizophrenia or schizoaffective disorder up to 39 European ancestry schizophrenia cases, up to 40 European ancestry schizoaffective cases NA Illumina [1190033] 21 antipsychotic drug use measurement http://www.ebi.ac.uk/efo/EFO_0007792 GCST003341 Genome-wide genotyping array 2016-02-12 25950743 Uttayamakul S 2015-06-15 AIDS Res Hum Retroviruses www.ncbi.nlm.nih.gov/pubmed/25950743 Genome-Wide Association Study of HIV-Related Lipoatrophy in Thai Patients: Association of a DLGAP1 Polymorphism with Fat Loss. Response to stavudine in HIV (lipoatrophy) 49 Thai ancestry cases, 92 Thai ancestry controls 95 Thai ancestry cases, 95 Thai ancestry controls Illumina [458071] 0 response to stavudine, Lipoatrophy http://www.ebi.ac.uk/efo/EFO_0006998, http://purl.obolibrary.org/obo/HP_0100578 GCST002968 Genome-wide genotyping array 2016-04-12 25948407 Kertai MD 2015-05-06 BMJ Open www.ncbi.nlm.nih.gov/pubmed/25948407 Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery. Perioperative myocardial infarction in coronary artery bypass surgery 112 cases, 1,321 controls 113 European ancestry cases, 509 European ancestry controls Illumina [534390] 15 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST002892 Genome-wide genotyping array 2016-07-06 25963972 Liu F 2015-05-12 Hum Genet www.ncbi.nlm.nih.gov/pubmed/25963972 Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Skin colour saturation 5,857 European ancestry individuals NA Illumina [11155022] (imputed) 7 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST002906 Genome-wide genotyping array 2016-07-06 25963972 Liu F 2015-05-12 Hum Genet www.ncbi.nlm.nih.gov/pubmed/25963972 Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Perceived skin darkness 9,316 European ancestry individuals 5,278 European ancestry individuals Illumina [up to 11155022] (imputed) 3 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST002907 Genome-wide genotyping array 2016-07-06 25963972 Liu F 2015-05-12 Hum Genet www.ncbi.nlm.nih.gov/pubmed/25963972 Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up. Skin sensitivity to sun 2,668 European ancestry individuals NA Illumina [NR] (imputed) 4 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST002908 Genome-wide genotyping array 2016-06-30 26030142 Van Driest SL 2015-06-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/26030142 Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy. Peak creatinine levels in vancomycin therapy 489 European ancestry individuals 439 European ancestry individuals Illumina [711284] 1 creatinine measurement, response to vancomycin http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0007647 GCST002948 Genome-wide genotyping array 2016-06-30 26030142 Van Driest SL 2015-06-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/26030142 Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy. Vancomycin trough in vancomycin therapy 745 European ancestry individuals 343 European ancestry individuals Illumina [711284] 0 vancomycin trough measurement, response to vancomycin http://www.ebi.ac.uk/efo/EFO_0007648, http://www.ebi.ac.uk/efo/EFO_0007647 GCST002946 Genome-wide genotyping array 2016-06-30 26030142 Van Driest SL 2015-06-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/26030142 Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy. Renal elimination rate in vancomycin therapy 745 European ancestry individuals 343 European ancestry individuals Illumina [711284] 0 renal elimination rate measurement, response to vancomycin http://www.ebi.ac.uk/efo/EFO_0007649, http://www.ebi.ac.uk/efo/EFO_0007647 GCST002947 Genome-wide genotyping array 2016-07-08 26031901 Dahlin A 2015-06-02 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/26031901 Genome-wide association study of leukotriene modifier response in asthma. Response to zileuton treatment in asthma (FEV1 change interaction) 160 European and other ancestry zileuton-treated cases, 144 European and other ancestry placebo-controlled cases 149 European and other ancestry zileuton-treated cases, 73 European and other ancestry placebo-controlled cases Illumina [542562] 21 FEV change measurement, response to zileuton http://www.ebi.ac.uk/efo/EFO_0005921, http://www.ebi.ac.uk/efo/EFO_0007676 GCST002951 Genome-wide genotyping array 2016-06-13 26348319 Myung W 2015-09-08 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/26348319 A genome-wide association study of antidepressant response in Koreans. Response to serotonin reuptake inhibitors in non-psychotic unipolar depression 263 Korean ancestry responder cases, 218 Korean ancestry non-responder cases 118 Korean ancestry responder cases, 112 Korean ancestry non-responder cases Affymetrix [505435] (imputed) 2 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST003118 Genome-wide genotyping array 2016-09-08 26333835 Scheinfeldt LB 2015-09-03 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26333835 Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration. Sleep duration up to 2,484 European ancestry individuals, up to 70 African American individuals, up to 2 Native American or Alaska Native ancestry individuals, up to 85 Asian American individuals, up to 7 Native Hawaiian or other Pacific islander individuals, up to 44 mixed ancestry individuals 1,032 European ancestry individuals, 98 African American individuals, 4 Native American or Alaska Native ancestry individuals, 43 Asian American individuals, 7 Native Hawaiian or other Pacific islander individuals, 78 mixed ancestry individuals Affymetrix [169252] 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST003112 Genome-wide genotyping array 2016-09-08 26333835 Scheinfeldt LB 2015-09-03 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26333835 Using the Coriell Personalized Medicine Collaborative Data to conduct a genome-wide association study of sleep duration. Sleep duration up to 2,484 European ancestry individuals, up to 70 African American individuals, up to 2 Native American or Alaska Native ancestry individuals, up to 85 Asian American individuals, up to 7 Native Hawaiian or other Pacific islander individuals, up to 44 mixed ancestry individuals NA Affymetrix [870428] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST003111 Genome-wide genotyping array 2016-02-12 26024889 Qayyum R 2015-05-30 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26024889 Genome-wide association study of platelet aggregation in African Americans. Platelet aggregation 825 African American individuals 119 African American individuals, 1,221 European ancestry individuals Illumina [802881] 0 platelet aggregation http://purl.obolibrary.org/obo/GO_0070527 GCST002939 Genome-wide genotyping array 2016-04-28 26028593 Li M 2015-06-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26028593 Identification of new susceptibility loci for IgA nephropathy in Han Chinese. IgA nephropathy 1,434 Han Chinese ancestry cases, 10,661 Han Chinese ancestry controls 6,879 Han Chinese ancestry cases, 9,019 Han Chinese ancestry controls Illumina [3792949] (imputed) 23 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST002943 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (high tone) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 270 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 pure tone hearing measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007617, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003040 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (0.25 kHz) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 270 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003039 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (0.5 kHz) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 270 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003037 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (1 kHz) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 6,162 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003041 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (2 kHz) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 270 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003032 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (4 kHz) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 6,162 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003035 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (8 kHz) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 270 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003034 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (low tone) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 270 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 pure tone hearing measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007617, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003036 Genome-wide genotyping array 2016-04-23 26188009 Vuckovic D 2015-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26188009 Genome-wide association analysis on normal hearing function identifies PCDH20 and SLC28A3 as candidates for hearing function and loss. Hearing function (medium tone) 2,155 Italian (founder/genetic isolate) individuals 481 Silk Road (founder/genetic isolate) individuals, 270 European ancestry individuals Affymetrix, Illumina [up to 38020975] (imputed) 0 pure tone hearing measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007617, http://www.ebi.ac.uk/efo/EFO_0007616 GCST003033 Genome-wide genotyping array 2016-06-10 26198393 Ziv E 2015-07-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26198393 Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients. Multiple myeloma (survival) 469 European ancestry cases, 25 African American cases, 27 Latino cases, 24 cases 1090 European ancestry cases Affymetrix, Illumina [6026834] (imputed) 1 overall survival, multiple myeloma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0001378 GCST003051 Genome-wide genotyping array 2016-10-11 26545240 Giri A 2015-11-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/26545240 Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative. Pelvic organ prolapse 793 African American cases, 948 African American controls, 606 Hispanic cases, 305 Hispanic controls NA Affymetrix [at least 730985] (imputed) 25 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST003226 Genome-wide genotyping array 2016-10-11 26545240 Giri A 2015-11-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/26545240 Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative. Pelvic organ prolapse (moderate/severe) 154 African American cases, 948 African American controls, 163 Hispanic cases, 305 Hispanic controls NA Affymetrix [at least 730985] (imputed) 33 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST003225 Genome-wide genotyping array 2016-06-02 26237428 Law MH 2015-08-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26237428 Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma. Cutaneous malignant melanoma 12,874 European ancestry cases, 23,203 European ancestry controls 785 European ancestry cases, 791 European ancestry controls, 2,331 cases, 2,415 controls Affymetrix, Illumina [at least 1569314] (imputed) 16 cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0000389 GCST003061 Genome-wide genotyping array 2016-07-10 26087016 Pappa I 2015-06-18 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26087016 A genome-wide approach to children's aggressive behavior: The EAGLE consortium. Early childhood aggressive behavior 15,668 European ancestry individuals NA Affymetrix, Illumina [up to 3856236] (imputed) 3 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST002984 Genome-wide genotyping array 2016-07-10 26087016 Pappa I 2015-06-18 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26087016 A genome-wide approach to children's aggressive behavior: The EAGLE consortium. Middle childhood and early adolescence aggressive behavior 16,311 European ancestry individuals NA Affymetrix, Illumina [up to 3856236] (imputed) 7 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST002985 Genome-wide genotyping array 2016-07-10 26087016 Pappa I 2015-06-18 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26087016 A genome-wide approach to children's aggressive behavior: The EAGLE consortium. Childhood and early adolescence aggressive behavior 18,988 European ancestry individuals NA Affymetrix, Illumina [up to 3856236] (imputed) 6 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST002986 Genome-wide genotyping array 2016-04-23 22550155 Edelstein LC 2012-05-01 Circulation www.ncbi.nlm.nih.gov/pubmed/22550155 Human genome-wide association and mouse knockout approaches identify platelet supervillin as an inhibitor of thrombus formation under shear stress. Platelet thrombus formation 125 European ancestry individuals, 116 African American individuals NA Illumina [at least 620901] 6 platelet reactivity measurement, thrombus formation measurement http://www.ebi.ac.uk/efo/EFO_0004985, http://www.ebi.ac.uk/efo/EFO_0007615 GCST001501 Genome-wide genotyping array 2016-10-14 26708676 Pulit SL 2015-12-18 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/26708676 Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. Ischemic stroke 14,300 European ancestry cases, 1,609 African ancestry cases, 942 Hispanic cases, 26,690 European ancestry controls, 3,354 African ancestry controls, 2,429 Hispanic controls 996 African ancestry cases, 219 East Asian ancestry cases, 17,334 European ancestry cases, 548 Hispanic cases, 2,385 South Asian ancestry cases, 5,811 African ancestry controls, 329 East Asian ancestry controls, 350,928 European ancestry controls, 686 Hispanic controls, 5,193 South Asian ancestry controls Illumina [up to 15400000] (imputed) 3 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST003258 Genome-wide genotyping array 2016-10-14 26708676 Pulit SL 2015-12-18 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/26708676 Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. Ischemic stroke (cardioembolic) up to 3,400 European ancestry cases, up to 208 African ancestry cases, up to 118 Hispanic cases, 26,690 European ancestry controls, 3,354 African ancestry controls, 2,429 Hispanic controls 98 African ancestry cases, 31 East Asian ancestry cases, 3,436 European ancestry cases, 97 Hispanic cases, 422 South Asian ancestry cases, 2,917 African ancestry controls, 329 East Asian ancestry controls, 274,063 European ancestry controls, 686 Hispanic controls, 5,193 South Asian ancestry controls Illumina [up to 15400000] (imputed) 2 Ischemic stroke, cardiac embolism http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_1001493 GCST003257 Genome-wide genotyping array 2016-10-14 26708676 Pulit SL 2015-12-18 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/26708676 Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. Ischemic stroke (large artery atherosclerosis) up to 2,349 European ancestry cases, up to 220 African ancestry cases, up to 146 Hispanic cases, 26,690 European ancestry controls, 3,354 African ancestry controls, 2,429 Hispanic controls 33 African ancestry cases, 34 East Asian ancestry cases, 1,787 European ancestry cases, 40 Hispanic ancestry cases, 355 South Asian ancestry cases, 239 African ancestry controls, 329 East Asian ancestry controls, 176,782 European ancestry controls, 686 Hispanic controls, 5,193 South Asian ancestry controls Illumina [up to 15400000] (imputed) 2 Ischemic stroke, large artery stroke http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0005524 GCST003259 Genome-wide genotyping array 2016-10-14 26708676 Pulit SL 2015-12-18 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/26708676 Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. Ischemic stroke (small artery occlusion) up to 2,252 European ancestry cases, up to 381 African ancestry cases, up to 552 Hispanic cases, 26,690 European ancestry controls, 3,354 African ancestry controls, 2,429 Hispanic controls 47 African ancestry cases, 133 East Asian ancestry cases, 1,847 European ancestry cases, 85 Hispanic cases, 314 South Asian ancestry cases, 239 African ancestry controls, 329 East Asian ancestry controls, 217,755 European ancestry controls, 686 Hispanic controls, 5,193 South Asian ancestry stroke controls Illumina [up to 15400000] (imputed) 1 Ischemic stroke, small artery occlusion http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_1001495 GCST003260 Genome-wide genotyping array 2016-10-14 26708676 Pulit SL 2015-12-18 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/26708676 Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study. Ischemic stroke (undetermined subtype) up to 8,062 European ancestry cases, up to 1,086 African ancestry cases, up to 362 Hispanic cases, 26,690 European ancestry controls, 3,354 African ancestry controls, 2,429 Hispanic controls 17 African ancestry cases, 17 East Asian ancestry cases, 3,514 European ancestry cases, 149 Hispanic cases, 239 African ancestry controls, 329 East Asian ancestry controls, 259,291 European ancestry controls, 686 Hispanic controls Illumina [up to 15400000] (imputed) 1 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST003261 Genome-wide genotyping array 2016-10-10 26691988 Fritsche LG 2015-12-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26691988 A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants. Advanced age-related macular degeneration 16,144 European ancestry cases, 17,832 European ancestry controls 473 Asian ancestry cases, 1,099 Asian ancestry controls, 52 African ancestry cases, 361 African ancestry cases, 254 other non-European ancestry cases, 694 other non-European ancestry controls Illumina [12023830] (imputed) 52 atrophic macular degeneration, age-related macular degeneration, wet macular degeneration http://www.ebi.ac.uk/efo/EFO_1001492, http://www.ebi.ac.uk/efo/EFO_0001365, http://www.ebi.ac.uk/efo/EFO_0004683 GCST003219 Genome-wide genotyping array 2016-12-16 26926045 Adhikari K 2016-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26926045 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Scalp hair shape 6,357 Latin American individuals NA Illumina [9143600] (imputed) 9 hair shape measurement http://www.ebi.ac.uk/efo/EFO_0007824 GCST003474 Genome-wide genotyping array 2016-12-16 26926045 Adhikari K 2016-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26926045 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Beard thickness 2,922 Latin American individuals NA Illumina [9143600] (imputed) 8 facial hair thickness measurement http://www.ebi.ac.uk/efo/EFO_0007823 GCST003475 Genome-wide genotyping array 2016-12-16 26926045 Adhikari K 2016-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26926045 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Eyebrow thickness 2,922 Latin American individuals NA Illumina [9143600] (imputed) 10 facial hair thickness measurement http://www.ebi.ac.uk/efo/EFO_0007823 GCST003476 Genome-wide genotyping array 2016-12-16 26926045 Adhikari K 2016-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26926045 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Monobrow thickness 2,922 Latin American individuals NA Illumina [9143600] (imputed) 7 facial hair thickness measurement http://www.ebi.ac.uk/efo/EFO_0007823 GCST003477 Genome-wide genotyping array 2016-12-16 26926045 Adhikari K 2016-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26926045 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Hair greying 6,357 Latin American individuals NA Illumina [9143600] (imputed) 8 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST003478 Genome-wide genotyping array 2016-12-16 26926045 Adhikari K 2016-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26926045 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Hair color 6,357 Latin American individuals NA Illumina [9143600] (imputed) 11 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST003479 Genome-wide genotyping array 2016-12-16 26926045 Adhikari K 2016-03-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26926045 A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features. Balding 6,357 Latin American individuals NA Illumina [9143600] (imputed) 2 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST003480 Genome-wide genotyping array 2016-10-10 26701879 Wang Z 2015-12-23 Gut www.ncbi.nlm.nih.gov/pubmed/26701879 Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies. Non-cardia gastric cancer 2,031 Han Chinese ancestry cases, 4,970 Han Chinese ancestry controls 3,564 Han Chinese ancestry cases, 4,637 Han Chinese ancestry controls Affymetrix, Illumina [6223896] (imputed) 6 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST003218 Genome-wide genotyping array 2016-05-12 25953783 Warrington NM 2015-05-07 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/25953783 A genome-wide association study of body mass index across early life and childhood. Body mass index (age interaction) 9,377 children and adolescents 3,918 European ancestry children and adolescents Illumina [~ 2200000] (imputed) 2 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST002893 Genome-wide genotyping array 2016-05-12 25953783 Warrington NM 2015-05-07 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/25953783 A genome-wide association study of body mass index across early life and childhood. Body mass index 9,377 children and adolescents 3,918 European ancestry children and adolescents Illumina [~ 2200000] (imputed) 9 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002894 Genome-wide genotyping array 2016-07-24 26192919 Liu JZ 2015-07-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26192919 Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. Ulcerative colitis 6,968 European ancestry cases, 20,464 European ancestry controls 10,679 European ancestry cases, 26,715 European ancestry controls, 397 Iranian ancestry cases, 342 Iranian ancestry controls, 1,239 Indian ancestry cases, 990 Indian ancestry controls, 1,134 East Asian ancestry cases, 3,719 East Asian ancestry controls Affymetrix, Illumina [~ 9000000] (imputed) 134 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST003045 Genome-wide genotyping array 2016-07-24 26192919 Liu JZ 2015-07-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26192919 Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. Crohn's disease 5,956 European ancestry cases, 14,927 European ancestry controls 14,594 European ancestry cases, 26,715 European ancestry controls, 151 Iranian ancestry cases, 342 Iranian ancestry controls, 184 Indian ancestry cases, 990 Indian ancestry controls, 1,690 East Asian ancestry cases, 3,719 East Asian ancestry controls Affymetrix, Illumina [~ 9000000] (imputed) 165 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST003044 Genome-wide genotyping array 2016-07-24 26192919 Liu JZ 2015-07-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26192919 Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. Inflammatory bowel disease 12,882 European ancestry cases, 21,770 European ancestry controls 25,273 European ancestry cases, 26,715 European ancestry controls, 548 Iranian ancestry cases, 342 Iranian ancestry control, 1,423 Indian ancestry cases, 990 Indian ancestry controls, 2,824 East Asian ancestry cases, 3,719 East Asian ancestry controls Affymetrix, Illumina [~ 9000000] (imputed) 202 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST003043 Genome-wide genotyping array 2016-12-08 26835600 Hu Y 2016-02-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26835600 GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person. Morning vs. evening chronotype 38,937 European ancestry morning chronotype individuals, 50,346 European ancestry evening chronotype individuals NA Illumina [7427422] (imputed) 77 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST003429 Genome-wide genotyping array 2016-12-08 26835600 Hu Y 2016-02-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26835600 GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person. Chronotype 38,937 European ancestry morning individuals, 50,346 European ancestry evening individuals, at least 32,842 European ancestry neutral individuals NA Illumina [7427422] (imputed) 2 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST003428 Genome-wide genotyping array 2016-05-31 26169577 Mosley JD 2015-07-14 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/26169577 A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. Cough in response to angiotensin-converting enzyme inhibitor drugs 1,346 European ancestry ACE inhibitor-exposed cases, 178 African ancestry ACE inhibitor-exposed cases, 71 ACE inhibitor-exposed cases, 4,661 European ancestry ACE inhibitor-exposed controls, 701 African ancestry ACE inhibitor-exposed controls, 123 ACE inhibitor-exposed controls 867 European ancestry ACE inhibitor-exposed cases, 4,364 European ancestry ACE inhibitor-exposed controls Illumina [1931830] (imputed) 1 response to angiotensin-converting enzyme inhibitor, Cough http://www.ebi.ac.uk/efo/EFO_0005325, http://purl.obolibrary.org/obo/HP_0012735 GCST003027 Genome-wide genotyping array 2016-07-08 25961943 Surakka I 2015-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25961943 The impact of low-frequency and rare variants on lipid levels. HDL cholesterol up to 62,166 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 9657952] (imputed) 42 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST002899 Genome-wide genotyping array 2016-07-08 25961943 Surakka I 2015-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25961943 The impact of low-frequency and rare variants on lipid levels. Triglycerides up to 62,166 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 9657952] (imputed) 35 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST002897 Genome-wide genotyping array 2016-07-08 25961943 Surakka I 2015-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25961943 The impact of low-frequency and rare variants on lipid levels. LDL cholesterol up 62,166 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 9657952] (imputed) 43 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST002898 Genome-wide genotyping array 2016-07-08 25961943 Surakka I 2015-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25961943 The impact of low-frequency and rare variants on lipid levels. Cholesterol, total up to 62,166 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 9657952] (imputed) 47 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST002896 Genome-wide genotyping array 2016-02-12 25956309 Palomba G 2015-05-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/25956309 Genome-wide association study of susceptibility loci for breast cancer in Sardinian population. Breast cancer 1,367 Sardinian cases, 1,658 Sardinian controls 201 Sardinian cases, 1,467 Sardinian controls, 61,485 European ancestry cases, 60,860 European ancestry controls Affymetrix [2067645] (imputed) 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST002895 Genome-wide genotyping array 2016-03-24 26007630 Swaminathan B 2015-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26007630 Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. Multiple myeloma 2,194 European ancestry cases, 222,555 European ancestry controls 586 European ancestry cases, 2,111 European ancestry controls Illumina [12100000] (imputed) 8 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST002921 Genome-wide genotyping array 2016-03-24 26007630 Swaminathan B 2015-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26007630 Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma. Multiple myeloma and monoclonal gammopathy 2,194 European ancestry multiple myeloma cases, 251 European ancestry monoclonal gammopathy cases, 294,390 European ancestry controls 586 European ancestry multiple myeloma cases, 2,111 European ancestry controls Illumina [12100000] (imputed) 9 multiple myeloma, monoclonal gammopathy http://www.ebi.ac.uk/efo/EFO_0001378, http://www.ebi.ac.uk/efo/EFO_0000203 GCST002922 Genome-wide genotyping array 2016-04-21 26015512 Komatsu M 2015-05-26 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/26015512 Pharmacoethnicity in Paclitaxel-Induced Sensory Peripheral Neuropathy. Paclitaxel-induced neuropathy 24 Japanese ancestry cases, 121 Japanese ancestry controls NA Illumina [733202] 0 peripheral neuropathy, methylcobalamin deficiency type cblE http://www.ebi.ac.uk/efo/EFO_0003100, http://purl.obolibrary.org/obo/MONDO_0009354 GCST002923 Genome-wide genotyping array 2016-04-21 26015512 Komatsu M 2015-05-26 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/26015512 Pharmacoethnicity in Paclitaxel-Induced Sensory Peripheral Neuropathy. Paclitaxel-induced cytotoxicity 57 Japanese ancestry lymphoblastoid cell lines, 59 Han Chinese ancestry lymphoblastoid cell lines 77 European ancestry lymphoblastoid cell lines, 87 Yoruban ancestry lymphoblastoid cell lines, 83 African ancestry lymphoblastoid cell lines NR [~ 4600000] (imputed) 3 methylcobalamin deficiency type cblE, cytotoxicity measurement http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0006952 GCST002924 Genome-wide genotyping array 2016-03-24 25987507 Minica CC 2015-05-19 Behav Genet www.ncbi.nlm.nih.gov/pubmed/25987507 Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset. Cannabis use (age at onset) 5,148 European ancestry users NA NR [5896100] (imputed) 9 Cannabis use, age at onset http://www.ebi.ac.uk/efo/EFO_0007585, http://www.ebi.ac.uk/efo/EFO_0004847 GCST002917 Genome-wide genotyping array 2016-03-24 25987507 Minica CC 2015-05-19 Behav Genet www.ncbi.nlm.nih.gov/pubmed/25987507 Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset. Cannabis use (initiation) 1,357 European ancestry users, 5,387 European ancestry never users NA NR [5896100] (imputed) 14 Cannabis use initiation http://www.ebi.ac.uk/efo/EFO_0007586 GCST002916 Genome-wide genotyping array 2016-02-19 25979521 de Jong K 2015-06-05 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/25979521 Genome-wide interaction study of gene-by-occupational exposure and effects on FEV1 levels. Forced expiratory volume in 1 second (occupational environmental exposures interaction) 12,400 individuals 1,436 individuals Illumina [up to 221663] 7 response to biological dust exposure, response to gases and fumes exposure, forced expiratory volume, response to mineral dust exposure http://www.ebi.ac.uk/efo/EFO_0006992, http://www.ebi.ac.uk/efo/EFO_0006994, http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0006993 GCST002955 Genome-wide genotyping array 2015-09-16 25096241 Keller MF 2014-08-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25096241 Trans-ethnic meta-analysis of white blood cell phenotypes. White blood cell count 16,843 Japanese ancestry individuals, 19,509 European ancestry individuals, 16,388 African American individuals NA Illumina [NR] (imputed) 16 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST002556 Genome-wide genotyping array 2015-09-22 25096241 Keller MF 2014-08-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25096241 Trans-ethnic meta-analysis of white blood cell phenotypes. Neutrophil count 9,802 Japanese ancestry individuals, 16,550 European ancestry individuals, 7,391 African American individuals NA Illumina [NR] (imputed) 9 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST002557 Genome-wide genotyping array 2015-09-16 25096241 Keller MF 2014-08-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25096241 Trans-ethnic meta-analysis of white blood cell phenotypes. Monocyte count 9,810 Japanese ancestry individuals, 16,550 European ancestry individuals, 7,369 African American individuals NA Illumina [NR] (imputed) 11 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST002555 Genome-wide genotyping array 2016-06-01 26169365 Huang KC 2015-07-14 BMC Complement Altern Med www.ncbi.nlm.nih.gov/pubmed/26169365 Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine. Yu-Zhi constitution type in type 2 diabetes 539 non-aboriginal Taiwanese ancestry low Yu-Zhi score individuals, 408 non-aboriginal Taiwanese ancestry high Yu-Zhi score individuals NA Illumina [508761] 11 Yu-Zhi constitution type http://www.ebi.ac.uk/efo/EFO_0007638 GCST003026 Genome-wide genotyping array 2016-06-17 26174136 Setoh K 2015-07-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26174136 Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels. Serum alpha1-antitrypsin levels 3,294 Japanese ancestry individuals 6,065 Japanese ancestry individuals Illumina [6569727] (imputed) 3 serum alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0005415 GCST003028 Genome-wide genotyping array 2016-04-01 26186006 Abrantes P 2015-07-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/26186006 Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal. Intracranial aneurysm 100 European ancestry cases, 92 European ancestry controls 100 European ancestry cases, 407 European ancestry controls Affymetrix [868261] 0 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST003038 Genome-wide genotyping array 2016-06-28 26174813 Alemany S 2015-07-14 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26174813 New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder. Attention function in attention deficit hyperactive disorder 479 European ancestry adult cases NA Illumina [799713] 25 attention function measurement http://www.ebi.ac.uk/efo/EFO_0007636 GCST003025 Genome-wide genotyping array 2016-04-26 26083729 Maruthur NM 2015-06-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/26083729 Genetics of Plasma Soluble Receptor for Advanced Glycation End-Products and Cardiovascular Outcomes in a Community-based Population: Results from the Atherosclerosis Risk in Communities Study. Advanced glycation end-product levels 581 Black individuals, 1,737 European ancestry individuals NA Affymetrix [up to 9100000] (imputed) 2 sRAGE measurement http://www.ebi.ac.uk/efo/EFO_0007622 GCST002977 Genome-wide genotyping array 2016-10-10 26528553 Davenport ER 2015-11-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/26528553 Genome-Wide Association Studies of the Human Gut Microbiota. Gut microbiome composition (summer) 91 Hutterite individuals NA Affymetrix [210924] 35 seasonal gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007753 GCST003221 Genome-wide genotyping array 2016-10-10 26528553 Davenport ER 2015-11-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/26528553 Genome-Wide Association Studies of the Human Gut Microbiota. Gut microbiome composition (summer and winter) 127 Hutterite individuals NA Affymetrix [212153] 9 seasonal gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007753 GCST003222 Genome-wide genotyping array 2016-10-10 26528553 Davenport ER 2015-11-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/26528553 Genome-Wide Association Studies of the Human Gut Microbiota. Gut microbiome composition (winter) 93 Hutterite individuals NA Affymetrix [211319] 33 seasonal gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007753 GCST003223 Genome-wide genotyping array 2016-12-07 26908436 Siiskonen SJ 2016-02-12 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/26908436 A Genome-Wide Association Study of Cutaneous Squamous Cell Carcinoma among European Descendants. Squamous cell carcinoma 745 European ancestry cases, 12,805 European ancestry controls 531 European ancestry cases, 551 European ancestry controls Affymetrix [2392512] (imputed) 5 squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707 GCST003422 Genome-wide genotyping array 2016-10-13 26865924 Lee M 2015-12-21 Nutr Res Pract www.ncbi.nlm.nih.gov/pubmed/26865924 Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight. Body mass index 40 Korean ancestry low BMI individuals, 37 Korean ancestry high BMI individuals NA Affymetrix [at least 710679] (imputed) 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST003248 Genome-wide genotyping array 2016-10-13 26865924 Lee M 2015-12-21 Nutr Res Pract www.ncbi.nlm.nih.gov/pubmed/26865924 Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight. Basal metabolic rate 39 Korean ancestry low BMR individuals, 38 Korean ancestry high BMR individuals NA Affymetrix [at least 710315] (imputed) 2 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST003249 Genome-wide genotyping array 2016-12-07 26912274 Zeng Y 2016-02-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26912274 Novel loci and pathways significantly associated with longevity. Longevity 2,178 Han Chinese ancestry centenarian cases, 2,299 Han Chinese ancestry middle-age controls NA Illumina [5595657] (imputed) 9 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST003425 Genome-wide genotyping array 2016-12-13 26876947 Saito T 2016-02-11 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26876947 Pharmacogenomic Study of Clozapine-Induced Agranulocytosis/Granulocytopenia in a Japanese Population. Clozapine-induced agranulocytosis/granulocytopenia in treatment-resistant schizophrenia 50 Japanese ancestry cases, 2905 Japanese ancestry controls NA Illumina [522694] 2 Drug-induced agranulocytosis, response to clozapine http://purl.obolibrary.org/obo/HP_0012235, http://purl.obolibrary.org/obo/GO_0097338 GCST003450 Genome-wide genotyping array 2015-11-14 25637581 Derringer J 2015-01-31 Behav Genet www.ncbi.nlm.nih.gov/pubmed/25637581 Genome-Wide Association Study of Behavioral Disinhibition in a Selected Adolescent Sample. Behavioral disinhibition 1,129 European ancestry individuals, 477 Hispanic individuals, 114 Black individuals, 42 Native American ancestry individuals, 40 Asian or Pacific Islander ancestry individuals, 99 individuals 3,378 European ancestry individuals Affymetrix [696388] 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST002768 Genome-wide genotyping array 2016-06-29 25663218 Verhaaren BF 2015-07-02 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25663218 Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI. White matter hyperintensity burden 17,936 European ancestry individuals, 1,943 African American ancestry individuals, 795 Hispanic individuals, 204 Chinese ancestry individuals, 201 Malay ancestry individuals NA Affymetrix, Illumina [14227402] (imputed) 36 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST003013 Genome-wide genotyping array 2015-05-18 25642632 Liu H 2015-02-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25642632 Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy. Leprosy 1,548 Chinese ancestry cases, 2,150 Chinese ancestry controls, 4,362 Chinese ancestry controls with immune-related diseases 6,765 Chinese ancestry cases, 9,505 Chinese ancestry controls Illumina [4577171] (imputed) 22 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST002772 Genome-wide genotyping array 2016-12-01 26879886 Wakil SM 2016-02-16 Clin Genet www.ncbi.nlm.nih.gov/pubmed/26879886 A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs. Low high density lipoprotein cholesterol levels 1,747 Saudi Arab ancestry cases, 2,335 Saudi Arab ancestry controls 517 Saudi Arab ancestry cases, 896 Saudi Arab ancestry controls Affymetrix [~ 8000000] (imputed) 11 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST003391 Genome-wide genotyping array 2016-10-06 26675016 Cha S 2015-12-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/26675016 A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans. Thoracic-to-hip circumference ratio 2,388 Korean ancestry males, 2,600 Korean ancestry females 767 Korean ancestry males, 1,485 Korean ancestry females Affymetrix [310746] 2 thoracic-to-hip circumference ratio measurement http://www.ebi.ac.uk/efo/EFO_0007769 GCST003197 Genome-wide genotyping array 2016-12-01 26818947 Imamura M 2016-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26818947 Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes. Type 2 diabetes 15,463 Japanese ancestry cases, 26,183 Japanese ancestry controls 20,490 East Asian ancestry cases, 22,922 East Asian ancestry controls, 38,947 European ancestry cases, 121,903 European ancestry controls, 10,587 South Asian ancestry cases, 14,378 South Asian ancestry controls, 3,848 Mexican/Latino cases, 4,366 Mexican/Latino controls Illumina [7521072] (imputed) 56 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST003400 Genome-wide genotyping array 2016-11-18 26785701 Wen W 2016-01-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26785701 Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference. Waist circumference up to 44,609 East Asian individuals up to 25,553 East Asian individuals, up to 230,044 individuals Affymetrix, Illumina [at least 1850000] (imputed) 8 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST003335 Genome-wide genotyping array 2016-11-18 26785701 Wen W 2016-01-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26785701 Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference. Waist-to-hip ratio adjusted for body mass index up to 39,869 East Asian individuals up to 20,137 East Asian individuals, up to 209,947 individuals Affymetrix, Illumina [at least 1850000] (imputed) 10 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST003338 Genome-wide genotyping array 2016-11-18 26785701 Wen W 2016-01-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26785701 Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference. Waist circumference adjusted for body mass index up to 44,609 East Asian individuals up to 24,146 East Asian individuals, up to 229,290 individuals Affymetrix, Illumina [at least 1850000] (imputed) 12 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST003336 Genome-wide genotyping array 2016-11-18 26785701 Wen W 2016-01-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26785701 Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference. Waist-hip ratio up to 39,869 East Asian individuals up to 25,553 East Asian individuals, up to 212,173 individuals Affymetrix, Illumina [at least 1850000] (imputed) 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST003337 Genome-wide genotyping array 2016-11-10 26780889 Below JE 2016-01-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26780889 Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. Cholesterol, total 4,383 Mexican ancestry individuals 7,876 Latin American/Hispanic individuals, European ancestry individuals (Global Lipids Genetics Consortium et al, 2013) Affymetrix [at least 370268] (imputed) 6 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST003302 Genome-wide genotyping array 2016-11-10 26780889 Below JE 2016-01-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26780889 Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. LDL cholesterol 4,383 Mexican ancestry individuals 7,876 Latin American/Hispanic individuals, European ancestry individuals (Global Lipids Genetics Consortium et al, 2013) Affymetrix [at least 370268] (imputed) 4 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST003303 Genome-wide genotyping array 2016-11-10 26780889 Below JE 2016-01-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26780889 Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. Triglycerides 4,383 Mexican ancestry individuals 7,876 Latin American/Hispanic individuals, European ancestry individuals (Global Lipids Genetics Consortium et al, 2013) Affymetrix [at least 370268] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST003301 Genome-wide genotyping array 2016-11-10 26780889 Below JE 2016-01-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26780889 Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs. HDL cholesterol 4,383 Mexican ancestry individuals 7,876 Latin American/Hispanic individuals, European ancestry individuals (Global Lipids Genetics Consortium et al, 2013) Affymetrix [at least 370268] (imputed) 7 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST003304 Genome-wide genotyping array 2016-12-08 26833246 Lu Y 2016-02-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26833246 New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk. Body fat percentage Up to 31,457 European ancestry men, up to 35,030 European ancestry women, up to 8,259 Indian Asian ancestry men, up to 1,030 Indian Asian ancestry women, 973 Korean ancestry men, 1,360 Korean ancestry women, 154 African American men, 262 African American women Up to 12,480 European ancestry men, up to 10,055 European ancestry women, 315 Jamaican ancestry men, 774 Jamaican ancestry women Affymetrix, Illumina, Perlegen [at least 1958375] (imputed) 47 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST003435 Genome-wide genotyping array 2016-08-05 26242244 Ma Y 2015-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26242244 Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. Exploratory eye movement dysfunction in schizophrenia (responsive search score) 128 Han Chinese ancestry cases NA Illumina [498648] 21 exploratory eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007700 GCST003065 Genome-wide genotyping array 2016-08-05 26242244 Ma Y 2015-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26242244 Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. Exploratory eye movement dysfunction in schizophrenia (total eye scanning length) 128 Han Chinese ancestry cases NA Illumina [498648] 8 exploratory eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007700 GCST003066 Genome-wide genotyping array 2016-08-05 26242244 Ma Y 2015-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26242244 Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. Exploratory eye movement dysfunction in schizophrenia (mean eye scanning length) 128 Han Chinese ancestry cases NA Illumina [498648] 2 exploratory eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007700 GCST003067 Genome-wide genotyping array 2016-08-05 26242244 Ma Y 2015-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26242244 Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. Exploratory eye movement dysfunction in schizophrenia (number of eye fixations) 128 Han Chinese ancestry cases NA Illumina [498648] 19 exploratory eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007700 GCST003068 Genome-wide genotyping array 2016-08-05 26242244 Ma Y 2015-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26242244 Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia. Exploratory eye movement dysfunction in schizophrenia (cognitive search score) 128 Han Chinese ancestry cases NA Illumina [498648] 15 exploratory eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007700 GCST003064 Genome-wide genotyping array 2016-12-19 26962152 Offenbacher S 2016-03-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26962152 Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease. Periodontal disease-related phenotype (Socransky) 394 European American individuals with periodontal health, 389 European American individuals with mild-moderate periodontitis, 192 European American individuals with severe periodontitis NA Affymetrix [2135235] (imputed) 6 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST003484 Genome-wide genotyping array 2019-08-16 26962152 Offenbacher S 2016-03-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26962152 Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease. Periodontal disease related phenotype (PCT2) 394 European American individuals with periodontal health, 389 European American individuals with mild-moderate periodontitis, 192 European American individuals with severe periodontitis NA Affymetrix [2135235] (imputed) 0 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST008439 Genome-wide genotyping array 2019-08-16 26962152 Offenbacher S 2016-03-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26962152 Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease. Periodontal disease related phenotype (PCT3) 394 European American individuals with periodontal health, 389 European American individuals with mild-moderate periodontitis, 192 European American individuals with severe periodontitis NA Affymetrix [2135235] (imputed) 2 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST008440 Genome-wide genotyping array 2019-08-16 26962152 Offenbacher S 2016-03-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26962152 Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease. Periodontal disease related phenotype (PCT4) 394 European American individuals with periodontal health, 389 European American individuals with mild-moderate periodontitis, 192 European American individuals with severe periodontitis NA Affymetrix [2135235] (imputed) 1 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST008441 Genome-wide genotyping array 2019-08-16 26962152 Offenbacher S 2016-03-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26962152 Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease. Periodontal disease related phenotype (PCT5) 394 European American individuals with periodontal health, 389 European American individuals with mild-moderate periodontitis, 192 European American individuals with severe periodontitis NA Affymetrix [2135235] (imputed) 3 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST008442 Genome-wide genotyping array 2019-08-16 26962152 Offenbacher S 2016-03-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26962152 Genome-wide association study of biologically informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease. Periodontal disease related phenotype (PCT6) 394 European American individuals with periodontal health, 389 European American individuals with mild-moderate periodontitis, 192 European American individuals with severe periodontitis NA Affymetrix [2135235] (imputed) 0 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST008443 Genome-wide genotyping array 2016-11-18 26763874 Ryu D 2016-01-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26763874 Genome-wide association study reveals sex-specific selection signals against autosomal nucleotide variants. Sex ratio 4,183 Korean ancestry male individuals, 4,659 Korean ancestry female individuals 935 Korean ancestry individuals Affymetrix [1400289] (imputed) 1 sex ratio http://www.ebi.ac.uk/efo/EFO_0004820 GCST003331 Genome-wide genotyping array 2016-10-13 26631737 Teumer A 2015-12-02 Diabetes www.ncbi.nlm.nih.gov/pubmed/26631737 Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes. Urinary albumin-to-creatinine ratio in diabetes up to 5,825 European ancestry cases up to 1,962 European ancestry cases Affymetrix, Illumina [2191945] (imputed) 2 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST003250 Genome-wide genotyping array 2016-10-14 26631737 Teumer A 2015-12-02 Diabetes www.ncbi.nlm.nih.gov/pubmed/26631737 Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes. Urinary albumin-to-creatinine ratio in non-diabetics up to 46,051 European ancestry individuals NA Affymetrix, Illumina [2191945] (imputed) 10 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST003254 Genome-wide genotyping array 2016-10-14 26631737 Teumer A 2015-12-02 Diabetes www.ncbi.nlm.nih.gov/pubmed/26631737 Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes. Microalbuminuria up to 54,116 European ancestry cases NA Affymetrix, Illumina [2191945] (imputed) 15 Moderate albuminuria http://purl.obolibrary.org/obo/HP_0012594 GCST003253 Genome-wide genotyping array 2016-10-14 26631737 Teumer A 2015-12-02 Diabetes www.ncbi.nlm.nih.gov/pubmed/26631737 Genome-wide Association Studies Identify Genetic Loci Associated With Albuminuria in Diabetes. Urinary albumin-to-creatinine ratio up to 54,450 European ancestry individuals NA Affymetrix, Illumina [2191945] (imputed) 12 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST003255 Genome-wide genotyping array 2016-09-02 26235824 Styrkarsdottir U 2015-08-29 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/26235824 Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland. Low bone mineral density (spine) 2,894 Icelandic cases, 206,485 Icelandic controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [24988228] (imputed) 1 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST003106 Genome-wide genotyping array 2016-09-02 26235824 Styrkarsdottir U 2015-08-29 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/26235824 Two Rare Mutations in the COL1A2 Gene Associate With Low Bone Mineral Density and Fractures in Iceland. Low bone mineral density (hip) 2,678 Icelandic cases, 206,701 Icelandic controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [24988228] (imputed) 1 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST003105 Genome-wide genotyping array 2016-02-13 26058915 Tin A 2015-05-29 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26058915 Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study. Magnesium levels 2,737 African American individuals 942 African American individuals Affymetrix [14825944] (imputed) 5 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST002933 Genome-wide genotyping array 2016-02-24 25963547 Wilson CL 2015-05-11 Cancer www.ncbi.nlm.nih.gov/pubmed/25963547 Genetic and clinical factors associated with obesity among adult survivors of childhood cancer: A report from the St. Jude Lifetime Cohort. Obesity in adult survivors of childhood cancer exposed to cranial radiation 365 obese individuals, 411 non-obese individuals NA Affymetrix [NR] (imputed) 4 response to radiation, obesity http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0001073 GCST002900 Genome-wide genotyping array 2016-02-24 25963547 Wilson CL 2015-05-11 Cancer www.ncbi.nlm.nih.gov/pubmed/25963547 Genetic and clinical factors associated with obesity among adult survivors of childhood cancer: A report from the St. Jude Lifetime Cohort. Obesity in adult survivors of childhood cancer not exposed to cranial radiation 359 obese individuals, 861 non-obese individuals NA Affymetrix [NR] (imputed) 1 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST002904 Genome-wide genotyping array 2016-04-21 26025128 Park HW 2015-05-27 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/26025128 Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts. Bone mineral accretion in asthma (oral corticosteroid dose interaction) 489 European ancestry children NA Illumina [NR] 9 bone mineral accretion measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0007591, http://purl.obolibrary.org/obo/GO_0031960 GCST002926 Genome-wide genotyping array 2016-02-24 25987655 Fernandez CA 2015-05-18 Blood www.ncbi.nlm.nih.gov/pubmed/25987655 Genome-wide analysis links NFATC2 with asparaginase hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 3,126 child cases 182 child cases Affymetrix [NR] 8 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST002915 Genome-wide genotyping array 2016-03-24 25987243 Parham LR 2015-05-19 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/25987243 Comprehensive genome-wide evaluation of lapatinib-induced liver injury yields a single genetic signal centered on known risk allele HLA-DRB1*07:01. Lapatinib-induced hepatotoxicity 775 European ancestry treated breast cancer cases, 236 East Asian ancestry treated breast cancer cases, 247 treated breast cancer cases NA Illumina [1085881] 3 response to lapatinib, drug-induced liver injury http://purl.obolibrary.org/obo/GO_0036274, http://www.ebi.ac.uk/efo/EFO_0004228 GCST002918 Genome-wide genotyping array 2016-06-10 26211971 Ogura Y 2015-07-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26211971 A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis. Adolescent idiopathic scoliosis 2,109 Japanese ancestry cases, 11,140 Japanese ancestry controls 2,223 East Asian ancestry cases, 4,724 East Asian ancestry controls Illumina [4420789] (imputed) 4 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST003052 Genome-wide genotyping array 2016-07-15 26190474 Dai Y 2015-07-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26190474 Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome. Trichloroethylene-induced hypersensitivity syndrome 98 Han Chinese ancestry cases, 98 Han Chinese ancestry trichloroethylene-tolerant controls Up to 74 Han Chinese ancestry cases, up to 1,661 Han Chinese ancestry trichloroethylene-tolerant controls Illumina [1392644] 3 trichloroethylene-induced hypersensitivity http://www.ebi.ac.uk/efo/EFO_0007685 GCST003046 Genome-wide genotyping array 2016-07-18 26183928 Leng S 2015-07-16 Cancer Res www.ncbi.nlm.nih.gov/pubmed/26183928 Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in Lung. MGMT methylation in smokers 296 European ancestry individuals with MGMT methylation, 867 European ancestry individuals without MGMT methylation 107 European and Hispanic individuals with MGMT methylation, 323 European and Hispanic individuals without MGMT methylation Illumina [1599980] 3 gene methylation measurement http://www.ebi.ac.uk/efo/EFO_0006959 GCST003031 Genome-wide genotyping array 2016-06-16 26184321 Lin BD 2015-07-13 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/26184321 Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Blond vs non-blond hair color 2,888 European ancestry blond hair individuals, 4,203 European ancestry non-blond hair individuals NA Affymetrix, Illumina, Perlegen [6473680] (imputed) 6 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST003023 Genome-wide genotyping array 2016-06-16 26184321 Lin BD 2015-07-13 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/26184321 Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Brown vs. non-brown hair color 3,826 European ancestry brown hair individuals, 3,265 European ancestry non-brown hair individuals NA Affymetrix, Illumina, Perlegen [6473680] (imputed) 8 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST003021 Genome-wide genotyping array 2016-06-16 26184321 Lin BD 2015-07-13 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/26184321 Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Light vs. dark hair color 3,069 European ancestry light hair individuals, 4,022 European ancestry dark hair individuals NA Affymetrix, Illumina, Perlegen [6473680] (imputed) 8 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST003022 Genome-wide genotyping array 2016-06-16 26184321 Lin BD 2015-07-13 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/26184321 Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Red vs non-red hair color 181 European ancestry red hair individuals, 6,910 European ancestry non-red hair individuals NA Affymetrix, Illumina, Perlegen [6473680] (imputed) 3 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST003020 Genome-wide genotyping array 2016-06-16 26184321 Lin BD 2015-07-13 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/26184321 Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample. Black vs. non-black hair color 196 European ancestry black hair individuals, 6,895 European ancestry non-black hair individuals NA Affymetrix, Illumina, Perlegen [6473680] (imputed) 2 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST003019 Genome-wide genotyping array 2016-06-16 26194203 Ramachandran D 2015-07-20 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/26194203 Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. Atrioventricular septal defects in Down syndrome 210 European ancestry cases with atrioventricular septal defects, 242 European ancestry cases with normal hearts NA Affymetrix [606195] 1 Atrioventricular canal defect http://purl.obolibrary.org/obo/HP_0006695 GCST003047 Genome-wide genotyping array 2016-11-18 26752265 Bailey JN 2016-01-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26752265 Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Glaucoma (primary open-angle) 3,853 European ancestry cases, 33,480 European ancestry controls 2,137 European ancestry cases, 6,699 European ancestry controls, 1,037 Singaporean Chinese ancestry cases, 2,543 Singaporean Chinese ancestry controls Affymetrix, Illumina [6425680] (imputed) 5 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST003342 Genome-wide genotyping array 2016-11-18 26752265 Bailey JN 2016-01-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26752265 Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Glaucoma (low intraocular pressure) 725 European ancestry cases, 11,145 European ancestry controls 363 European ancestry cases Affymetrix, Illumina [6425680] (imputed) 3 low tension glaucoma http://www.ebi.ac.uk/efo/EFO_1001022 GCST003343 Genome-wide genotyping array 2016-11-18 26752265 Bailey JN 2016-01-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26752265 Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma. Glaucoma (high intraocular pressure) 1,868 European ancestry cases, 31,497 European ancestry controls Affymetrix, Illumina [6425680] (imputed) 6 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST003344 Genome-wide genotyping array 2016-11-24 26763881 Kurano M 2016-01-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26763881 Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride. Triglyceride levels 2,994 Japanese ancestry individuals 6,805 Korean ancestry individuals Illumina [1294241] 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST003364 Genome-wide genotyping array 2016-11-24 26763881 Kurano M 2016-01-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26763881 Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride. HDL cholesterol levels 2,994 Japanese ancestry individuals 6,805 Korean ancestry individuals Illumina [1294241] 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST003363 Genome-wide genotyping array 2016-11-24 26763881 Kurano M 2016-01-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26763881 Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride. LDL cholesterol levels 2,994 Japanese ancestry individuals 6,805 Korean ancestry individuals Illumina [1294241] 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST003361 Genome-wide genotyping array 2016-11-24 26763881 Kurano M 2016-01-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26763881 Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride. Phospholipid levels 2,994 Japanese ancestry individuals 6,805 Korean ancestry individuals Illumina [1294241] 0 phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004639 GCST003362 Genome-wide genotyping array 2016-12-13 26767831 Grant AV 2016-01-14 Hum Genet www.ncbi.nlm.nih.gov/pubmed/26767831 A genome-wide association study of pulmonary tuberculosis in Morocco. Tuberculosis up to 42 Moroccan ancestry affected parents, 210 Moroccan ancestry unaffected parents, up to 239 Moroccan ancestry affected offspring and 67 Moroccan ancestry unaffected offspring from 135 families up to 317 Moroccan ancestry cases, 650 Moroccan ancestry controls Illumina [5390648] (imputed) 1 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST003451 Genome-wide genotyping array 2016-10-05 26685716 Chang X 2015-12-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26685716 Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children. Magnesium levels 2,267 European American children 257 European American children, 15,366 European ancestry adults Illumina [at least 507409] (imputed) 2 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST003195 Genome-wide genotyping array 2016-10-06 26686025 Hwang JY 2015-12-12 Bone www.ncbi.nlm.nih.gov/pubmed/26686025 Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population. Calcaneal bone ultrasound measurement (speed of sound) 1,895 Korean ancestry individuals 7,263 Korean ancestry individuals Illumina [NR] (imputed) 1 calcaneal bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0007772 GCST003196 Genome-wide genotyping array 2016-11-30 26766742 Garcia-Albeniz X 2016-01-14 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/26766742 CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk. Colorectal cancer (menopausal hormone therapy interaction) 1,436 European ancestry postmenopausal cases, 1,948 European ancestry postmenopausal controls NA Affymetrix, Illumina [~ 2700000] (imputed) 0 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST003385 Genome-wide genotyping array 2016-11-30 26766742 Garcia-Albeniz X 2016-01-14 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/26766742 CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk. Colorectal cancer (oestrogen-progestogen hormone therapy interaction) 554 European ancestry postmenopausal cases, 729 European ancestry postmenopausal controls NA Affymetrix, Illumina [~ 2700000] (imputed) 1 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST003386 Genome-wide genotyping array 2016-11-30 26766742 Garcia-Albeniz X 2016-01-14 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/26766742 CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk. Colorectal cancer (oestrogen hormone therapy interaction) 650 European ancestry postmenopausal cases, 956 European ancestry postmenopausal controls NA Affymetrix, Illumina [~ 2700000] (imputed) 0 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST003387 Genome-wide genotyping array 2016-10-06 26782385 Zhou TQ 2015-12-21 Genet Mol Res www.ncbi.nlm.nih.gov/pubmed/26782385 Genome-wide analysis of single nucleotide polymorphisms in patients with atrophic age-related macular degeneration in oldest old Han Chinese. Atrophic age-related macular degeneration 30 Han Chinese ancestry elderly (>95 years old) cases, 47 Han Chinese ancestry elderly (>95 years old) controls 208 Han Chinese ancestry cases, 218 Han Chinese ancestry controls Affymetrix [561277] 0 atrophic macular degeneration http://www.ebi.ac.uk/efo/EFO_1001492 GCST003199 Genome-wide genotyping array 2016-06-08 26030696 Cho MH 2015-06-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26030696 A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes. Percentage gas trapping 3,243 European ancestry chronic obstructive pulmonary disease cases, 901 African American chronic obstructive pulmonary disease cases, 3,062 European ancestry controls, 2,132 African American controls NA Illumina [6900000] (imputed) 17 gas trapping measurement http://www.ebi.ac.uk/efo/EFO_0007628 GCST002942 Genome-wide genotyping array 2016-06-08 26030696 Cho MH 2015-06-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26030696 A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes. Airway imaging phenotypes 5,385 European ancestry chronic obstructive pulmonary disease cases, 901 African American chronic obstructive pulmonary disease cases, 3,613 European ancestry controls, 2,132 African American controls NA Illumina [7600000] (imputed) 14 airway imaging measurement http://www.ebi.ac.uk/efo/EFO_0007627 GCST002941 Genome-wide genotyping array 2016-06-08 26030696 Cho MH 2015-06-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26030696 A Genome-Wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes. Emphysema imaging phenotypes 5,385 European ancestry chronic obstructive pulmonary disease cases, 901 African American chronic obstructive pulmonary disease cases, 3,613 European ancestry controls, 2,132 African American controls NA Illumina [7600000] (imputed) 52 emphysema imaging measurement http://www.ebi.ac.uk/efo/EFO_0007626 GCST002945 Genome-wide genotyping array 2016-12-13 26955885 Lane JM 2016-03-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26955885 Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank. Chronotype 100,420 European ancestry individuals NA Affymetrix [~ 73355677] (imputed) 14 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST003453 Genome-wide genotyping array 2016-12-13 26955885 Lane JM 2016-03-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26955885 Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank. Morning vs. evening chronotype 8,724 European ancestry evening chronotype individuals, 26,948 European ancestry morning chronotype individuals NA Affymetrix [73355677] (imputed) 10 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST003454 Genome-wide genotyping array 2016-07-20 26222057 Pander J 2015-07-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/26222057 Genome Wide Association Study for Predictors of Progression Free Survival in Patients on Capecitabine, Oxaliplatin, Bevacizumab and Cetuximab in First-Line Therapy of Metastatic Colorectal Cancer. Progression free survival in metastatic colorectal cancer (CAPOX-B vs CAPOX-B plus cetuximab) 256 cases treated with CAPOX-B plus cetuximab, 264 cases treated with CAPOX-B NA Illumina [2850023] (imputed) 3 progression free survival, metastatic colorectal cancer, response to cetuximab, response to CAPOX-B http://www.ebi.ac.uk/efo/EFO_0004920, http://www.ebi.ac.uk/efo/EFO_1001480, http://www.ebi.ac.uk/efo/EFO_0007682, http://www.ebi.ac.uk/efo/EFO_0007683 GCST003058 Genome-wide genotyping array 2016-07-20 26222057 Pander J 2015-07-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/26222057 Genome Wide Association Study for Predictors of Progression Free Survival in Patients on Capecitabine, Oxaliplatin, Bevacizumab and Cetuximab in First-Line Therapy of Metastatic Colorectal Cancer. Progression free survival in metastatic colorectal cancer (chemotherapy interaction) 256 cases treated with CAPOX-B plus cetuximab, 264 cases treated with CAPOX-B NA Illumina [2850023] (imputed) 1 progression free survival, metastatic colorectal cancer, response to cetuximab, response to CAPOX-B http://www.ebi.ac.uk/efo/EFO_0004920, http://www.ebi.ac.uk/efo/EFO_1001480, http://www.ebi.ac.uk/efo/EFO_0007682, http://www.ebi.ac.uk/efo/EFO_0007683 GCST003057 Genome-wide genotyping array 2016-04-28 26049409 Hirano A 2015-06-05 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26049409 A genome-wide association study of late-onset Alzheimer's disease in a Japanese population. Alzheimer's disease (late onset) 489 Japanese ancestry APOE-ε4 noncarrier cases, 6,463 Japanese ancestry APOE-ε4 noncarrier controls, 323 Japanese ancestry APOE-ε4 carrier cases, 1,484 Japanese ancestry APOE-ε4 carrier controls, 4 Japanese ancestry cases, 45 Japanese ancestry controls 528 Japanese ancestry APOE-ε4 noncarrier cases, 5,824 Japanese ancestry APOE-ε4 noncarrier controls, 480 Japanese ancestry APOE-ε4 carrier cases, 1,364 Japanese ancestry APOE-ε4 carrier controls, 3 Japanese ancestry cases, 24 Japanese ancestry controls Illumina [561143] 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002954 Genome-wide genotyping array 2016-02-11 25963331 Hatzimanolis A 2015-05-12 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/25963331 Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood. Endophenotypes for schizophrenia in healthy individuals 1,079 European ancestry male cases 1,563 European ancestry male cases Affymetrix [5654592] (imputed) 0 endophenotype http://www.ebi.ac.uk/efo/EFO_0006988 GCST002905 Genome-wide genotyping array 2016-02-13 25990418 Al-Tassan NA 2015-05-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/25990418 A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer. Colorectal cancer 7,577 European ancestry cases, 9,979 European ancestry controls NA Affymetrix, Illumina [~ 10000000] (imputed) 19 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002919 Genome-wide genotyping array 2016-07-06 25993607 de Moor MH 2015-05-20 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/25993607 Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder. Neuroticism Up to 627 Cilento (founder/genetic isolate) individuals, up to 2,296 Erasmus Rucphen (founder/genetic isolate) individuals, up to 1,650 Orcadian (founder/genetic isolate) individuals, up to 909 Vis (founder/genetic isolate) individuals, up to 58,179 European ancestry individuals Up to 9,786 European ancestry individuals Affymetrix, Illumina, Perlegen [6949614] (imputed) 12 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST002920 Genome-wide genotyping array 2015-11-21 25763902 Draaken M 2015-03-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25763902 Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy. Classic bladder exstrophy 208 European ancestry cases, 1,703 European ancestry controls NA Illumina [7261187] (imputed) 25 bladder exstrophy http://purl.obolibrary.org/obo/MONDO_0010805 GCST002807 Genome-wide genotyping array 2016-02-11 25986216 Toyoda H 2015-05-15 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/25986216 A polymorphism in CCR1/CCR3 is associated with narcolepsy. Narcolepsy with cataplexy 409 Japanese ancestry cases, 1,562 Japanese ancestry controls 240 Japanese ancestry cases, 869 Japanese ancestry controls Affymetrix [525196] 4 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST002912 Genome-wide genotyping array 2016-07-11 26220383 Jang HW 2015-06-02 Epilepsy Res www.ncbi.nlm.nih.gov/pubmed/26220383 GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. Epilepsy and lamotrigine-induced maculopapular eruptions 34 Korean ancestry cases, 1,080 Korean ancestry healthy controls NA Affymetrix [4893794] (imputed) 27 response to lamotrigine, maculopapular eruption, epilepsy http://www.ebi.ac.uk/efo/EFO_0007661, http://www.ebi.ac.uk/efo/EFO_1001253, http://www.ebi.ac.uk/efo/EFO_0000474 GCST002949 Genome-wide genotyping array 2016-07-11 26220383 Jang HW 2015-06-02 Epilepsy Res www.ncbi.nlm.nih.gov/pubmed/26220383 GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy. Epilepsy 130 Korean ancestry cases, 1,081 Korean ancestry controls NA Affymetrix [at least 323735] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST002950 Genome-wide genotyping array 2016-06-13 26081443 Adkins DE 2015-06-17 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/26081443 Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood. Longitudinal alcohol consumption 2,126 adolescents and early adults NA Illumina [866099] (imputed) 6 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST002981 Genome-wide genotyping array 2015-07-17 24975945 Ganesh SK 2014-06-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24975945 Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations. Blood pressure 46,553 European ancestry individuals 34,433 European ancestry individuals, 5,605 Han Chinese ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 0 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST002506 Genome-wide genotyping array 2016-12-12 26980576 Kim K 2016-03-15 J Rheumatol www.ncbi.nlm.nih.gov/pubmed/26980576 Response to Intravenous Cyclophosphamide Treatment for Lupus Nephritis Associated with Polymorphisms in the FCGR2B-FCRLA Locus. Response to cyclophosphamide in systemic lupus erythematosus with lupus nephritis 93 Korean ancestry responder cases, 16 Korean ancestry non-responder cases NA Illumina [491617] 14 response to cyclophosphamide http://purl.obolibrary.org/obo/GO_1902518 GCST003445 Genome-wide genotyping array 2016-12-15 26956414 Berndt SI 2016-03-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26956414 Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia. Chronic lymphocytic leukemia 3,100 European ancestry cases, 7,667 European ancestry controls 1,958 cases, 5,530 controls Affymetrix, Illumina [~ 8500000] (imputed) 31 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST003468 Genome-wide genotyping array 2016-11-17 26829030 Asgari MM 2016-01-29 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/26829030 Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma. Squamous cell carcinoma 6,891 European ancestry cases, 54,566 European ancestry controls 810 European ancestry cases, 5,600 European ancestry controls Affymetrix [9610468] (imputed) 12 squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707 GCST003327 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Nickel levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 28 blood nickel measurement http://www.ebi.ac.uk/efo/EFO_0007583 GCST002928 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Chromium levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 19 blood chromium measurement http://www.ebi.ac.uk/efo/EFO_0007579 GCST002929 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Cobalt levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 19 blood cobalt measurement http://www.ebi.ac.uk/efo/EFO_0007577 GCST002930 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Aluminium levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 16 blood aluminium measurement http://www.ebi.ac.uk/efo/EFO_0007575 GCST002931 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Manganese levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 37 blood manganese measurement http://www.ebi.ac.uk/efo/EFO_0007581 GCST002932 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Molybdenum levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 17 blood molybdenum measurement http://www.ebi.ac.uk/efo/EFO_0007582 GCST002937 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Lead levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 28 blood lead measurement http://www.ebi.ac.uk/efo/EFO_0007040 GCST002935 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Zinc levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 24 blood zinc measurement http://www.ebi.ac.uk/efo/EFO_0007584 GCST002934 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Mercury levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 24 blood mercury measurement http://www.ebi.ac.uk/efo/EFO_0007580 GCST002927 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Cadmium levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 30 blood cadmium measurement http://www.ebi.ac.uk/efo/EFO_0007576 GCST002936 Genome-wide genotyping array 2016-03-24 26025379 Ng E 2015-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26025379 Genome-wide association study of toxic metals and trace elements reveals novel associations. Copper levels 949 European ancestry individuals NA Illumina [8736858] (imputed) 42 blood copper measurement http://www.ebi.ac.uk/efo/EFO_0007578 GCST002938 Genome-wide genotyping array 2016-04-28 25964295 Khan S 2015-05-11 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/25964295 Polymorphism at 19q13.41 Predicts Breast Cancer Survival Specifically after Endocrine Therapy. Survival in breast cancer (estrogen-receptor positive) 639 European ancestry cases 3,372 European ancestry cases Illumina [486478] 0 survival time, estrogen-receptor positive breast cancer, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305 GCST002903 Genome-wide genotyping array 2016-04-28 25964295 Khan S 2015-05-11 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/25964295 Polymorphism at 19q13.41 Predicts Breast Cancer Survival Specifically after Endocrine Therapy. Survival in breast cancer (estrogen-receptor negative) 597 European ancestry cases 1,351 European ancestry cases Illumina [486478] 0 estrogen-receptor negative breast cancer, survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST002902 Genome-wide genotyping array 2016-04-28 25964295 Khan S 2015-05-11 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/25964295 Polymorphism at 19q13.41 Predicts Breast Cancer Survival Specifically after Endocrine Therapy. Survival in endocrine treated breast cancer (estrogen-receptor positive) 352 European ancestry cases with endocrine therapy, 254 European ancestry cases without endocrine therapy, 597 European ancestry controls 3,330 European ancestry cases with endocrine therapy, 42 European ancestry cases without endocrine therapy, 1,351 European ancestry controls Illumina [486478] 1 survival time, estrogen-receptor positive breast cancer, breast carcinoma, response to endocrine therapy http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0007613 GCST002901 Genome-wide genotyping array 2017-02-24 26969751 Parmar PG 2016-03-11 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26969751 International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents. Diastolic blood pressure 5,008 European ancestry prepubescent females, 5,082 European ancestry prepubescent males, 4,238 European ancestry pubescent females, 4,185 European ancestry pubescent males, 2,680 European ancestry post-pubescent females, 2,496 European ancestry post-pubescent males NA Affymetrix, Illumina, Perlegen [NR] (imputed) 12 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST003671 Genome-wide genotyping array 2017-02-24 26969751 Parmar PG 2016-03-11 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/26969751 International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents. Systolic blood pressure 5,008 European ancestry prepubescent females, 5,082 European ancestry prepubescent males, 4,238 European ancestry pubescent females, 4,185 European ancestry pubescent males, 2,680 European ancestry post-pubescent females, 2,496 European ancestry post-pubescent males NA Affymetrix, Illumina, Perlegen [NR] (imputed) 16 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST003670 Genome-wide genotyping array 2016-12-08 26950853 Dehghan A 2016-03-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26950853 Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium. Incident coronary heart disease 2406 European ancestry cases, 21,618 European ancestry controls 3059 European ancestry cases, 28,087 European ancestry controls Affymetrix, Illumina [2543842] (imputed) 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST003431 Genome-wide genotyping array 2016-12-08 26950853 Dehghan A 2016-03-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/26950853 Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium. Incident myocardial infarction 1,570 European ancestry cases, at least 21,618 European ancestry controls 2,328 European ancestry cases, 546 African American ancestry cases, 7655 African American ancestry controls, up to 35,233 European ancestry controls Affymetrix, Illumina [2543842] (imputed) 4 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST003430 Genome-wide genotyping array 2017-02-24 26977737 Cade BE 2016-03-15 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26977737 Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. Obstructive sleep apnea trait (apnea hypopnea index) 12,558 Hispanic/Latin American individuals 214 Asian ancestry individuals, 1,183 African American individuals, 5,638 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 12 sleep apnea measurement, obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0007817, http://www.ebi.ac.uk/efo/EFO_0003918 GCST003674 Genome-wide genotyping array 2017-02-24 26977737 Cade BE 2016-03-15 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26977737 Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. Obstructive sleep apnea (average oxygen saturation during sleep) 12,557 Hispanic/Latin American ancestry individuals 214 Asian ancestry individuals, 1,183 African American ancestry individuals, 5,638 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 5 sleep apnea measurement, obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0007817, http://www.ebi.ac.uk/efo/EFO_0003918 GCST003673 Genome-wide genotyping array 2017-02-24 26977737 Cade BE 2016-03-15 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/26977737 Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. Obstructive sleep apnea trait (average respiratory event duration) 10,238 Hispanic/Latin American ancestry individuals 214 Asian ancestry individuals, 1,183 African American ancestry individuals, 5,638 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 14 sleep apnea measurement, obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0007817, http://www.ebi.ac.uk/efo/EFO_0003918 GCST003675 Genome-wide genotyping array 2016-09-07 26265699 Karol SE 2015-08-11 Blood www.ncbi.nlm.nih.gov/pubmed/26265699 Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia. Glucocorticoid-induced osteonecrosis (time dependent analysis) 164 European ancestry osteonecrosis cases, 4 Black osteonecrosis cases, 58 Hispanic osteonecrosis cases, 5 Asian ancestry osteonecrosis cases, 19 other ancestry osteonecrosis cases, 1,111 European ancestry treated controls, 135 Black treated controls, 543 Hispanic treated controls, 43 Asian ancestry treated controls, 203 other ancestry treated controls NA Affymetrix, Illumina [NR] (imputed) 3 response to glucocorticoid, osteonecrosis http://purl.obolibrary.org/obo/GO_0051384, http://www.ebi.ac.uk/efo/EFO_0004259 GCST003083 Genome-wide genotyping array 2016-09-07 26265699 Karol SE 2015-08-11 Blood www.ncbi.nlm.nih.gov/pubmed/26265699 Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia. Glucocorticoid-induced osteonecrosis (time independent analysis) 235 osteonecrosis cases, 1,687 treated controls 110 European ancestry osteonecrosis cases, 21 Black osteonecrosis cases, 10 Hispanic osteonecrosis cases, 1 Asian ancestry osteonecrosis case, 8 other ancestry osteonecrosis cases, 366 European ancestry treated controls, 88 Black treated controls, 29 Hispanic treated controls, 5 Asian ancestry treated controls, 32 other ancestry treated controls Affymetrix, Illumina [NR] (imputed) 0 response to glucocorticoid, osteonecrosis http://purl.obolibrary.org/obo/GO_0051384, http://www.ebi.ac.uk/efo/EFO_0004259 GCST003080 Genome-wide genotyping array 2016-09-07 26265699 Karol SE 2015-08-11 Blood www.ncbi.nlm.nih.gov/pubmed/26265699 Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia. Glucocorticoid-induced osteonecrosis (age 10 years and older) 230 osteonecrosis cases, 1,238 treated controls NA Affymetrix, Illumina [NR] (imputed) 11 response to glucocorticoid, osteonecrosis http://purl.obolibrary.org/obo/GO_0051384, http://www.ebi.ac.uk/efo/EFO_0004259 GCST003081 Genome-wide genotyping array 2016-09-07 26265699 Karol SE 2015-08-11 Blood www.ncbi.nlm.nih.gov/pubmed/26265699 Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia. Glucocorticoid-induced osteonecrosis 274 European ancestry osteonecrosis cases, 25 Black osteonecrosis cases, 68 Hispanic osteonecrosis cases, 6 Asian ancestry osteonecrosis cases, 27 other ancestry osteonecrosis cases, 1,477 European ancestry treated controls, 223 Black treated controls, 572 Hispanic treated controls, 48 Asian ancestry treated controls, 235 other ancestry treated controls NA Affymetrix, Illumina [NR] (imputed) 10 response to glucocorticoid, osteonecrosis http://purl.obolibrary.org/obo/GO_0051384, http://www.ebi.ac.uk/efo/EFO_0004259 GCST003084 Genome-wide genotyping array 2016-12-08 26859814 den Braber A 2016-02-09 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/26859814 Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs. Obsessive-compulsive symptoms 6,931 individuals NA Affymetrix, Illumina, Perlegen [31265038] (imputed) 13 obsessive-compulsive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007802 GCST003434 Genome-wide genotyping array 2016-11-17 26840454 French JD 2016-01-31 Oncotarget www.ncbi.nlm.nih.gov/pubmed/26840454 Germline polymorphisms in an enhancer of PSIP1 are associated with progression-free survival in epithelial ovarian cancer. Progression free survival in serous epithelial ovarian cancer treated with carboplatin and paclitaxel 279 European ancestry cases 965 European ancestry cases Illumina [6860000] (imputed) 0 progression free survival, response to carboplatin, methylcobalamin deficiency type cblE, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0004920, http://purl.obolibrary.org/obo/GO_0097328, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0001075 GCST003328 Genome-wide genotyping array 2016-10-05 26870257 Qu LS 2015-11-23 Oncol Lett www.ncbi.nlm.nih.gov/pubmed/26870257 Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study. Hepatocellular carcinoma in hepatitis B infection 50 Han Chinese ancestry seropositive cases, 50 Han Chinese ancestry seropositive controls 282 Han Chinese ancestry seropositive cases, 278 Han Chinese ancestry seropositive controls Affymetrix [279757] 2 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST003189 Genome-wide genotyping array 2016-08-31 26297903 Fabbri C 2015-08-20 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26297903 Genetics of long-term treatment outcome in bipolar disorder. Manic episodes in bipolar disorder 706 European ancestry cases NA Affymetrix [329806] (imputed) 3 manic or hypomanic episode http://www.ebi.ac.uk/efo/EFO_0007706 GCST003089 Genome-wide genotyping array 2016-08-31 26297903 Fabbri C 2015-08-20 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26297903 Genetics of long-term treatment outcome in bipolar disorder. Depressive episodes in bipolar disorder 723 European ancestry cases NA Affymetrix [329806] (imputed) 7 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST003091 Genome-wide genotyping array 2016-08-31 26297903 Fabbri C 2015-08-20 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26297903 Genetics of long-term treatment outcome in bipolar disorder. Depressive and manic episodes in bipolar disorder 723 European ancestry cases NA Affymetrix [329806] 7 manic episode measurement, depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0007704 GCST003090 Genome-wide genotyping array 2016-12-08 26856250 Sacchetti E 2016-02-09 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/26856250 The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis. Early response to risperidone in schizophrenia 86 European ancestry cases NA Affymetrix [350796] 1 response to risperidone http://purl.obolibrary.org/obo/GO_0097336 GCST003432 Genome-wide genotyping array 2015-07-28 25188341 Beecham GW 2014-09-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25188341 Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Dementia and core Alzheimer's disease neuropathologic changes up to 3,887 cases, up to 1,027 controls NA Affymetrix, Illumina [NR] (imputed) 51 dementia, Alzheimer's disease neuropathologic change http://purl.obolibrary.org/obo/MONDO_0001627, http://www.ebi.ac.uk/efo/EFO_0006801 GCST002593 Genome-wide genotyping array 2015-07-28 25188341 Beecham GW 2014-09-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25188341 Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Neurofibrillary tangles up to 4,707 individuals NA Affymetrix, Illumina [NR] (imputed) 37 neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006797 GCST002594 Genome-wide genotyping array 2015-07-28 25188341 Beecham GW 2014-09-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25188341 Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Neuritic plaque up to 4,232 individuals NA Affymetrix, Illumina [NR] (imputed) 34 neuritic plaque measurement http://www.ebi.ac.uk/efo/EFO_0006798 GCST002592 Genome-wide genotyping array 2015-07-28 25188341 Beecham GW 2014-09-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25188341 Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Lewy body disease up to 3,526 individuals NA Affymetrix, Illumina [NR] (imputed) 40 Lewy body dementia, Lewy body dementia measurement http://www.ebi.ac.uk/efo/EFO_0006792, http://www.ebi.ac.uk/efo/EFO_0006799 GCST002591 Genome-wide genotyping array 2015-07-28 25188341 Beecham GW 2014-09-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25188341 Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Vascular brain injury up to 2,940 individuals NA Affymetrix, Illumina [NR] (imputed) 21 vascular brain injury measurement, vascular brain injury http://www.ebi.ac.uk/efo/EFO_0006800, http://www.ebi.ac.uk/efo/EFO_0006791 GCST002590 Genome-wide genotyping array 2015-07-28 25188341 Beecham GW 2014-09-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25188341 Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Hippocampal sclerosis 310 cases, 2,576 controls NA Affymetrix, Illumina [NR] (imputed) 29 hippocampal sclerosis of aging http://www.ebi.ac.uk/efo/EFO_0005678 GCST002589 Genome-wide genotyping array 2015-07-28 25188341 Beecham GW 2014-09-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25188341 Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias. Cerebral amyloid angiopathy 1,673 cases, 1,134 controls NA Affymetrix, Illumina [NR] (imputed) 7 cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0006790 GCST002588 Genome-wide genotyping array 2016-07-14 26053186 Park SL 2015-06-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/26053186 Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 3-hydroxypropylmercapturic acid levels in smokers 362 African American current smoker individuals, 329 Native Hawaiian ancestry current smoker individuals, 438 European ancestry current smoker individuals, 449 Latino current smoker individuals, 704 Japanese ancestry current smoker individuals NA Illumina [up to 11892802] (imputed) 246 3-hydroxypropylmercapturic acid measurement http://www.ebi.ac.uk/efo/EFO_0007014 GCST002956 Genome-wide genotyping array 2016-07-13 26053186 Park SL 2015-06-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/26053186 Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer. 3-hydroxy-1-methylpropylmercapturic acid levels in smokers 361 African American current smoker individuals, 329 Native Hawaiian ancestry current smoker individuals, 440 European ancestry current smoker individuals, 452 Latino current smoker individuals, 702 Japanese ancestry current smoker individuals NA Illumina [up to 11892802] (imputed) 240 3-hydroxy-1-methylpropylmercapturic acid measurement http://www.ebi.ac.uk/efo/EFO_0007015 GCST002957 Genome-wide genotyping array 2016-02-11 25988933 Almli LM 2015-05-18 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/25988933 A genome-wide identified risk variant for PTSD is a methylation quantitative trait locus and confers decreased cortical activation to fearful faces. Post-traumatic stress disorder 32 Hispanic ancestry cases, 16 Black cases, 14 European ancestry cases, 1 other ancestry case, 25 Hispanic ancestry controls, 6 Asian ancestry controls, 19 Black controls, 31 European ancestry controls, 3 other ancestry controls 2,868 African American ancestry individuals Illumina [557423] 0 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST002914 Genome-wide genotyping array 2015-11-21 25972035 Vinayagamoorthy N 2015-05-14 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25972035 Association of common variants in the calcium-sensing receptor gene with serum calcium levels in East Asians. Calcium levels 4,558 Korean ancestry individuals 4,093 Korean ancestry individuals Affymetrix [1219546] (imputed) 12 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST002911 Genome-wide genotyping array 2016-07-01 25985088 Oguchi T 2015-05-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25985088 Investigation of susceptibility genes triggering lachrymal/salivary gland lesion complications in Japanese patients with type 1 autoimmune pancreatitis. Lachrymal/Salivary gland lesion in type 1 autoimmune pancreatitis 50 Japanese ancestry cases with lesions, 53 Japanese ancestry cases without lesions NA Affymetrix [12033] 2 salivary gland lesion, lachrymal gland lesion http://www.ebi.ac.uk/efo/EFO_0007124, http://www.ebi.ac.uk/efo/EFO_0007125 GCST002913 Genome-wide genotyping array 2015-08-13 24487271 Weizman A 2014-03-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/24487271 Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients. Pyoderma gangrenosum in inflammatory bowel disease 92 European ancestry cases, 5,664 European ancestry controls NA Illumina [2017629] (imputed) 7 pyoderma gangrenosum http://www.ebi.ac.uk/efo/EFO_0006835 GCST002379 Genome-wide genotyping array 2015-08-13 24487271 Weizman A 2014-03-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/24487271 Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients. Erythema nodosum in inflammatory bowel disease 103 European ancestry cases, 5,653 European ancestry controls NA Illumina [2017629] (imputed) 5 Erythema nodosum http://purl.obolibrary.org/obo/HP_0012219 GCST002380 Genome-wide genotyping array 2016-04-23 26029870 Ye Z 2015-06-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26029870 Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma. Sporadic pituitary adenoma 771 Han Chinese cases, 2,788 Han Chinese controls 2,542 Han Chinese cases, 3,620 Han Chinese controls Illumina [720770] 4 Pituitary Gland Adenoma http://www.ebi.ac.uk/efo/EFO_1000478 GCST002940 Genome-wide genotyping array 2016-02-12 25967671 Li C 2015-05-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25967671 Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese. Gout 1,255 Han Chinese ancestry male cases, 1,848 Han Chinese ancestry male controls 3,020 Han Chinese ancestry male cases, 4,424 Han Chinese ancestry male controls Affymetrix [603505] 5 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST002909 Genome-wide genotyping array 2016-02-12 26014426 Ruth KS 2015-05-27 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26014426 Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes. Sex hormone levels up to 2913 European ancestry individuals NA Illumina [7879351] (imputed) 15 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST002925 Genome-wide genotyping array 2016-05-17 26146898 Clark SL 2015-07-04 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/26146898 Combined Whole Methylome and Genomewide Association Study Implicates CNTN4 in Alcohol Use. Alcohol consumption 580 European ancestry cases, 39 European ancestry controls 689 European ancestry cases, 41 European ancestry controls Affymetrix [5571786] (imputed) 0 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST003015 Genome-wide genotyping array 2016-07-15 26188370 Burdon KP 2015-07-19 Diabetologia www.ncbi.nlm.nih.gov/pubmed/26188370 Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene. Sight-threatening diabetic retinopathy in type 2 diabetes 336 European ancestry cases with retinopathy, 508 European ancestry cases without retinopathy 263 European ancestry cases with retinopathy, 320 European ancestry cases without retinopathy, 334 South Asian ancestry cases with retinopathy, 365 South Asian ancestry cases without retinopathy Illumina [602755] 1 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST003042 Genome-wide genotyping array 2016-07-18 26184070 Aebi M 2015-07-16 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/26184070 Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder. Oppositional defiant disorder dimensions in attention-deficit hyperactivity disorder 750 European ancestry child and adolescent cases NA Perlegen [1871025] (imputed) 10 oppositional defiant disorder measurement http://www.ebi.ac.uk/efo/EFO_0007679 GCST003030 Genome-wide genotyping array 2015-09-19 25089948 Theusch E 2014-10-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/25089948 Ancestry and other genetic associations with plasma PCSK9 response to simvastatin. Response to simvastatin treatment (PCSK9 protein level change) 562 European ancestry individuals 287 African American individuals Illumina [570422] 7 response to simvastatin, PCSK9 protein measurement http://purl.obolibrary.org/obo/GO_1903491, http://www.ebi.ac.uk/efo/EFO_0006899 GCST002642 Genome-wide genotyping array 2016-06-28 26176695 Warrier V 2015-07-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/26176695 A Pooled Genome-Wide Association Study of Asperger Syndrome. Asperger syndrome 294 European ancestry cases, 318 European ancestry controls NA Affymetrix [NR] 0 Asperger syndrome http://www.ebi.ac.uk/efo/EFO_0003757 GCST003029 Genome-wide genotyping array 2016-07-18 26209787 Barthold JS 2015-07-24 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/26209787 Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functions. Cryptorchidism 844 European ancestry cases, 2,718 European ancestry controls 298 European ancestry cases, 324 European ancestry controls Illumina [at least 631140] (imputed) 0 cryptorchidism http://www.ebi.ac.uk/efo/EFO_0004562 GCST003053 Genome-wide genotyping array 2016-06-17 26545630 Deming Y 2015-09-25 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/26545630 A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin. Cerebrospinal fluid clusterin levels 300 Alzheimer's disease cases, 373 controls NA Illumina [5970354] (imputed) 24 cerebrospinal fluid clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007657 GCST003134 Genome-wide genotyping array 2016-06-17 26545630 Deming Y 2015-09-25 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/26545630 A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin. Plasma clusterin levels 521 Alzheimer's disease cases, 297 controls NA Illumina [5970354] (imputed) 15 plasma clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007656 GCST003133 Genome-wide genotyping array 2016-06-17 26545630 Deming Y 2015-09-25 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/26545630 A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin. Cerebrospinal fluid clusterin levels in APOEe4- carriers 123 Alzheimer's disease cases, 270 controls NA Illumina [5970354] (imputed) 1 cerebrospinal fluid clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007657 GCST003137 Genome-wide genotyping array 2016-06-17 26545630 Deming Y 2015-09-25 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/26545630 A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin. Cerebrospinal fluid clusterin levels in APOEe4+ carriers 177 Alzheimer's disease cases, 103 controls NA Illumina [5970354] (imputed) 1 cerebrospinal fluid clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007657 GCST003131 Genome-wide genotyping array 2016-09-12 26249676 Wolthusen RP 2015-08-07 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26249676 Genetic underpinnings of left superior temporal gyrus thickness in patients with schizophrenia. Left superior temporal gyrus thickness (schizophrenia interaction) 113 schizophrenia cases, 126 controls NA Illumina [1067955] (imputed) 6 schizophrenia, left superior temporal gyrus thickness measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0007739 GCST003069 Genome-wide genotyping array 2016-05-31 26174610 Kwak TJ 2015-07-14 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/26174610 Identification of a possible susceptibility locus for UVB-induced skin tanning phenotype in Korean females using genomewide association study. Ultraviolet-induced skin pigmentation (minimal erythema dose) 99 Korean ancestry individuals 112 Korean ancestry individuals Affymetrix [506945] 0 minimal erythema dose http://www.ebi.ac.uk/efo/EFO_0007639 GCST003024 Genome-wide genotyping array 2016-08-17 26265036 Parra EJ 2015-08-12 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/26265036 Genome-wide association study of warfarin maintenance dose in a Brazilian sample. Warfarin maintenance dose 180 Brazilian ancestry low dose individuals, 187 Brazilian ancestry high dose individuals 798 European ancestry individuals, 1611 Japanese ancestry individuals, 191 African American individuals Affymetrix [> 650000] (imputed) 16 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST003085 Genome-wide genotyping array 2016-08-31 26301688 Li YR 2015-08-24 Nat Med www.ncbi.nlm.nih.gov/pubmed/26301688 Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases. Pediatric autoimmune diseases 97 European ancestry thyroiditis cases, 107 European ancestry ankylosing spondylitis cases, 100 European ancestry psoriasis cases, 173 European ancestry celiac disease cases, 254 European ancestry systemic lupus erythematosus cases, 308 European ancestry common variable inmunodeficiency cases, 865 European ancestry ulcerative colitis cases, 1,086 European ancestry Type 1 diabetes cases, 1,123 European ancestry juvenile idiopathic arthritis cases, 1,922 European ancestry Crohn's disease cases, 10,718 European ancestry controls NA Illumina [7347414] (imputed) 46 autoimmune thyroid disease, systemic lupus erythematosus, type 1 diabetes mellitus, ankylosing spondylitis, psoriasis, common variable immunodeficiency, celiac disease, ulcerative colitis, Crohn's disease, autoimmune disease, juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0006812, http://purl.obolibrary.org/obo/MONDO_0007915, http://purl.obolibrary.org/obo/MONDO_0005147, http://www.ebi.ac.uk/efo/EFO_0003898, http://www.ebi.ac.uk/efo/EFO_0000676, http://purl.obolibrary.org/obo/MONDO_0015517, http://www.ebi.ac.uk/efo/EFO_0001060, http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0000384, http://www.ebi.ac.uk/efo/EFO_0005140, http://www.ebi.ac.uk/efo/EFO_0002609 GCST003097 Genome-wide genotyping array 2015-09-22 25648963 Debette S 2014-11-25 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25648963 Genome-wide studies of verbal declarative memory in nondemented older people: the Cohorts for Heart and Aging Research in Genomic Epidemiology consortium. Verbal declarative memory Up to 27,337 European ancestry individuals, up to 472 Korkulan individuals, up to 1,267 Erasmus Rucphen Family individuals Up to 10,617 European ancestry individuals, up to 3,811 African American individuals Affymetrix, Illumina [NR] (imputed) 43 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST002701 Genome-wide genotyping array 2016-02-12 25939597 Berndt SI 2015-05-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25939597 Two susceptibility loci identified for prostate cancer aggressiveness. Prostate cancer 4,600 European ancestry cases, 2,941 European ancestry controls 7,779 European ancestry cases, 7,623 European ancestry controls Illumina [1531807] (imputed) 18 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002890 Genome-wide genotyping array 2016-02-13 25939597 Berndt SI 2015-05-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25939597 Two susceptibility loci identified for prostate cancer aggressiveness. Prostate cancer aggressiveness 4,545 European ancestry cases 7,973 European ancestry cases Illumina [1531807] (imputed) 3 cancer aggressiveness measurement, Gleason score measurement, prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0006999, http://www.ebi.ac.uk/efo/EFO_0007000, http://www.ebi.ac.uk/efo/EFO_0001663 GCST002886 Genome-wide genotyping array 2015-07-08 25390645 Otowa T 2014-11-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/25390645 Genome-wide and gene-based association studies of anxiety disorders in European and African American samples. Anxiety disorder 324 African American cases, 273 African American controls, 757 European ancestry cases, 940 European ancestry controls NA Affymetrix [up to 730090] 15 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST002696 Genome-wide genotyping array 2012-11-19 23067351 Rasmussen-Torvik LJ 2012-08-23 Clin Transl Sci www.ncbi.nlm.nih.gov/pubmed/23067351 High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE. LDL cholesterol 1,249 African American individuals NA Illumina [910341] 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST001645 Genome-wide genotyping array 2014-08-02 24375517 Lohmann K 2013-12-26 Mov Disord www.ncbi.nlm.nih.gov/pubmed/24375517 Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus? Musician's dystonia 127 European ancestry cases, 984 European ancestry controls 116 European ancestry cases, 125 European ancestry controls Affymetrix [557620] 3 Limb dystonia http://www.orpha.net/ORDO/Orphanet_93957 GCST002319 Genome-wide genotyping array 2012-12-21 23022100 Franceschini N 2012-09-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23022100 Discovery and fine mapping of serum protein loci through transethnic meta-analysis. Serum total protein levels Up to 25,539 European ancestry individuals, 10,168 Japanese ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 12 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST001698 Genome-wide genotyping array 2012-12-21 23022100 Franceschini N 2012-09-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23022100 Discovery and fine mapping of serum protein loci through transethnic meta-analysis. Serum albumin levels Up to 53,190 European ancestry individuals, 9,380 Japanese ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 16 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST001699 Genome-wide genotyping array 2013-01-16 23064961 Shaffer JR 2012-10-11 J Dent Res www.ncbi.nlm.nih.gov/pubmed/23064961 GWAS of dental caries patterns in the permanent dentition. Dental caries 920 European ancestry individuals NA Illumina [518997] 32 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST001713 Genome-wide genotyping array 2014-11-26 24837172 Juyal G 2014-05-16 Gut www.ncbi.nlm.nih.gov/pubmed/24837172 Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis. Ulcerative colitis 603 North Indian ancestry cases, 622 North Indian ancestry controls 733 North Indian ancestry cases, 1,148 North Indian ancestry controls Illumina [480391] 5 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST002453 Genome-wide genotyping array 2015-06-26 25261932 Cerhan JR 2014-09-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25261932 Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma. Diffuse large B cell lymphoma 3,857 European ancestry cases, 7,666 European ancestry controls 1,359 European ancestry cases, 4,557 European ancestry controls Illumina [8363971] (imputed) 8 diffuse large B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000403 GCST002636 Genome-wide genotyping array 2008-06-16 17934461 Broderick P 2007-10-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17934461 A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. Colorectal cancer 930 European ancestry cases, 960 European ancestry controls 7,473 European ancestry cases, 5,984 European ancestry controls Illumina [547647] 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000113 Genome-wide genotyping array 2015-07-07 25284319 Sanchez-Mora C 2014-10-06 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/25284319 Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder. Persistent attention-deficit hyperactivity disorder 607 European ancestry adult cases, 584 European ancestry adult controls 2,104 European ancestry adult cases, 1,901 European ancestry adult controls Illumina [794090] 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST002648 Genome-wide genotyping array 2014-03-26 24046328 Bradley DT 2013-09-17 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24046328 A variant in LDLR is associated with abdominal aortic aneurysm. Abdominal aortic aneurysm 1,755 European ancestry cases, 5,314 European ancestry controls 1,658 European ancestry cases, 28,962 European ancestry controls, 1,725 cases, 3,791 controls Illumina [503892] 1 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST002193 Genome-wide genotyping array 2012-11-19 22925353 Lee HJ 2012-08-25 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/22925353 A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder. Bipolar disorder 2,191 European ancestry cases, 1,434 European ancestry controls NA Affymetrix [703012] 15 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001647 Genome-wide genotyping array 2016-01-27 25781442 Nan H 2015-03-17 JAMA www.ncbi.nlm.nih.gov/pubmed/25781442 Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants. Colorectal cancer (aspirin and/or NSAID use interaction) 8,634 European ancestry cases, 8,553 European ancestry controls NA Affymetrix, Illumina [2700000] (imputed) 2 drug use measurement, aspirin use measurement, NSAID use measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0007010, http://www.ebi.ac.uk/efo/EFO_0007013, http://www.ebi.ac.uk/efo/EFO_0007012, http://purl.obolibrary.org/obo/MONDO_0005575 GCST002816 Genome-wide genotyping array 2015-06-24 25353672 Fernandez-Navarro P 2014-10-29 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/25353672 Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21. Mammographic density 239 European ancestry low mammographic density females, 239 European ancestry high mammographic density females NA Illumina [575374] 5 mammographic density measurement http://www.ebi.ac.uk/efo/EFO_0005941 GCST002676 Genome-wide genotyping array 2014-07-29 24325915 Purrington KS 2013-12-09 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/24325915 Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer. Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) 1,529 European ancestry cases, 3,399 European ancestry controls 2,148 European ancestry cases, 1,309 European ancestry controls Illumina [NR] (imputed) 5 triple-negative breast cancer http://www.ebi.ac.uk/efo/EFO_0005537 GCST002305 Genome-wide genotyping array 2015-01-21 24957906 Kuiper JJ 2014-06-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24957906 A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy. Birdshot chorioretinopathy 117 European ancestry cases, 693 European ancestry controls 30 European ancestry cases, 2,793 European ancestry controls Illumina [9932851] (imputed) 3 birdshot chorioretinopathy http://purl.obolibrary.org/obo/MONDO_0011599 GCST002501 Genome-wide genotyping array 2011-09-23 21835309 Larsson M 2011-08-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21835309 GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development. Iris characteristics 2,121 European ancestry individuals 499 European ancestry adolescent twins and siblings, 73 European ancestry adult individuals Illumina [274604] (imputed) 7 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST001199 Genome-wide genotyping array 2011-06-18 21647700 Below JE 2011-06-07 Diabetologia www.ncbi.nlm.nih.gov/pubmed/21647700 Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals. Type 2 diabetes 837 Mexican American cases, 436 Mexican American controls 967 Mexican ancestry cases, 343 Mexican ancestry controls Affymetrix [1829586] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001092 Genome-wide genotyping array 2013-05-24 23406172 Milton JN 2013-02-14 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/23406172 Genetic determinants of haemolysis in sickle cell anaemia. Sickle cell anemia (haemolysis) 1,117 individuals 213 African ancestry, West African ancestry and Afro-Caribbean individuals, 745 individuals Illumina [569554] 4 sickle cell anemia http://purl.obolibrary.org/obo/MONDO_0011382 GCST001862 Genome-wide genotyping array 2014-01-10 23844046 Dorajoo R 2013-07-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/23844046 Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore? C-reactive protein 2,179 Chinese ancestry individuals, 2,275 Malay ancestry individuals, 2,238 Asian Indian ancestry individuals NA Illumina [up to 1745429] (imputed) 4 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST002086 Genome-wide genotyping array 2014-03-26 24047826 Kleber ME 2013-09-18 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24047826 Genome-wide association study identifies 3 genomic loci significantly associated with serum levels of homoarginine: the AtheroRemo Consortium. Homoarginine levels 5,143 European ancestry individuals 1,474 European ancestry individuals Affymetrix, Illumina [2543887] (imputed) 1 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST002196 Genome-wide genotyping array 2010-10-05 20835236 Hysi PG 2010-09-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20835236 A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. Refractive error 4,270 European ancestry individuals 13,414 European ancestry individuals Illumina [~ 2200000] (imputed) 1 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST000794 Genome-wide genotyping array 2010-09-28 20818381 Yamauchi T 2010-09-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20818381 A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. Type 2 diabetes 4,470 Japanese ancestry cases, 3,071 Japanese ancestry controls 10,692 Japanese ancestry cases, 9,597 Japanese ancestry controls, 6,980 European ancestry cases, 8,615 European ancestry controls Illumina [459359] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000787 Genome-wide genotyping array 2015-08-13 25705158 Shim U 2014-12-31 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/25705158 Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts. Metabolic syndrome 3,253 Korean ancestry cases, 5,589 Korean ancestry controls NA Affymetrix [312121] 2 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST002732 Genome-wide genotyping array 2016-01-22 25820613 Warrington NM 2015-03-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25820613 Genome-wide association study of blood lead shows multiple associations near ALAD. Lead levels in blood 5,433 individuals NA Illumina [6391392] (imputed) 15 blood lead measurement http://www.ebi.ac.uk/efo/EFO_0007040 GCST002831 Genome-wide genotyping array 2015-11-13 25722978 Borghese B 2015-02-04 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/25722978 Identification of susceptibility genes for peritoneal, ovarian, and deep infiltrating endometriosis using a pooled sample-based genome-wide association study. Endometriosis 20 European ancestry peritoneal endometriosis cases, 20 European ancestry endometrioma cases, 20 European ancestry deep infiltrating endometriosis cases, 20 European ancestry controls 42 European ancestry peritoneal endometriosis cases, 121 European ancestry endometrioma cases, 96 European ancestry deep infiltrating endometriosis cases, 288 European ancestry controls Affymetrix [262000] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST002776 Genome-wide genotyping array 2015-08-01 25705162 Oh JH 2014-12-31 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/25705162 Genome-wide association study identifies candidate Loci associated with platelet count in koreans. Platelet count 8,842 Korean ancestry individuals 7,861 Korean ancestry individuals Affymetrix [2152228] (imputed) 3 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST002733 Genome-wide genotyping array 2016-01-15 25706626 Aung T 2015-02-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25706626 A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome. Exfoliation syndrome 1,484 Japanese ancestry cases, 1,188 Japanese ancestry controls 1,530 East Asian ancestry cases, 6,230 East Asian ancestry controls, 1,064 Southern Indian ancestry cases, 3,536 Southern Indian ancestry controls, 140 Hispanic cases, 233 Hispanic controls, 347 Middle Eastern ancestry cases, 1,108 Middle Eastern ancestry controls, 3,588 European ancestry cases, 9,012 European ancestry controls, 102 South African Black cases, 379 South African Black controls, 50 Uighur cases, 49 Uighur controls, 80 cases, 180 controls Illumina [581023] 4 exfoliation syndrome http://www.ebi.ac.uk/efo/EFO_0004235 GCST002787 Genome-wide genotyping array 2015-11-21 25710658 Diouf B 2015-02-24 JAMA www.ncbi.nlm.nih.gov/pubmed/25710658 Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia. Vincristine-induced peripheral neuropathy in acute lymphoblastic leukemia 53 European ancestry cases with peripheral neuropathy, 156 cases without peripheral neuropathy, 10 African ancestry cases with peripheral neuropathy, 33 African ancestry cases without peripheral neuropathy, 1 Asian ancestry case with peripheral neuropathy, 1 Asian ancestry case without peripheral neuropathy, 14 Hispanic cases with peripheral neuropathy, 30 Hispanic cases without peripheral neuropathy, 8 cases with peripheral neuropathy, 15 cases without peripheral neuropathy NA Affymetrix [1576016] (imputed) 5 peripheral neuropathy, response to vincristine http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0006950 GCST002792 Genome-wide genotyping array 2015-12-18 25649181 Noordam R 2015-01-20 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/25649181 Identifying genetic loci associated with antidepressant drug response with drug-gene interaction models in a population-based study. Depressive symptoms (SSRI exposure interaction) 175 users, 6,268 nonusers NA Illumina [NR] (imputed) 10 drug use measurement, depressive symptom measurement, SSRI use measurement http://www.ebi.ac.uk/efo/EFO_0007010, http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007011 GCST002755 Genome-wide genotyping array 2015-08-08 25705159 Hong Y 2014-12-31 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/25705159 Genome-wide association study of hepatitis in korean populations. Hepatitis 1,500 Korean ancestry cases, 1,500 Korean ancestry controls NA NR [352000] 9 Hepatitis http://purl.obolibrary.org/obo/HP_0012115 GCST002730 Genome-wide genotyping array 2015-11-06 25628336 Hromatka BS 2015-01-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25628336 Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis. Motion sickness 80,494 European ancestry individuals NA Illumina [7428049] (imputed) 35 motion sickness http://www.ebi.ac.uk/efo/EFO_0006928 GCST002759 Genome-wide genotyping array 2016-01-05 25628645 Tong Y 2015-01-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/25628645 Identification of genetic variants or genes that are associated with Homoharringtonine (HHT) response through a genome-wide association study in human lymphoblastoid cell lines (LCLs). Response to Homoharringtonine (cytotoxicity) 93 African American ancestry lymphoblastoid cell lines, 91 European ancestry lymphoblastoid cell lines, 94 Han Chinese ancestry lymphoblastoid cell lines NA Affymetrix, Illumina [6750581] (imputed) 10 response to homoharringtonine, cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0006996, http://www.ebi.ac.uk/efo/EFO_0006952 GCST002749 Genome-wide genotyping array 2015-11-03 25616667 Goris A 2015-01-22 Brain www.ncbi.nlm.nih.gov/pubmed/25616667 Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. Oligoclonal band status in multiple sclerosis 2,232 European ancestry OCB positive individuals, 275 European ancestry OCB negative individuals, 439 OCB positive individuals, 80 OCB negative individuals 3,026 OCB positive individuals, 452 OCB negative individuals NR [485522] 3 oligoclonal band measurement http://www.ebi.ac.uk/efo/EFO_0005206 GCST002758 Genome-wide genotyping array 2015-11-03 25616667 Goris A 2015-01-22 Brain www.ncbi.nlm.nih.gov/pubmed/25616667 Genetic variants are major determinants of CSF antibody levels in multiple sclerosis. Immunoglobulin G index levels in multiple sclerosis 773 European ancestry Individuals, 165 Individuals 2,072 Individuals NR [485236] 3 IgG index http://www.ebi.ac.uk/efo/EFO_0006929 GCST002757 Genome-wide genotyping array 2015-11-17 25665007 Xu H 2015-02-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25665007 Common variants in ACYP2 influence susceptibility to cisplatin-induced hearing loss. Cisplatin-induced hearing loss in brain tumor patients 156 European ancestry cases, 82 African American and other ancestry cases 68 cases Illumina [1716999] 0 ototoxicity, hearing loss, response to cisplatin http://www.ebi.ac.uk/efo/EFO_0006951, http://www.ebi.ac.uk/efo/EFO_0004238, http://purl.obolibrary.org/obo/GO_0072718 GCST002780 Genome-wide genotyping array 2015-11-21 25713168 Leng S 2015-02-23 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/25713168 15q12 variants, sputum gene promoter hypermethylation, and lung cancer risk: a GWAS in smokers. Gene methylation in lung tissue 1,163 European ancestry smoker individuals 718 European ancestry smoker individuals Illumina [1599980] 3 gene methylation measurement http://www.ebi.ac.uk/efo/EFO_0006959 GCST002786 Genome-wide genotyping array 2016-02-12 25939698 Tsoi LC 2015-05-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25939698 Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci. Psoriasis 3,994 European ancestry cases, 7,699 European ancestry controls 6,268 European ancestry cases, 14,172 European ancestry controls, 5,033 cases, 5,707 controls Illumina [696365] (imputed) 6 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST002889 Genome-wide genotyping array 2016-02-11 25935875 Varenhorst C 2015-05-02 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/25935875 Effect of genetic variations on ticagrelor plasma levels and clinical outcomes. Ticagrelor levels in individuals with acute coronary syndromes treated with ticagrelor 1,794 European ancestry cases, 18 African and Asian ancestry cases 1,922 European ancestry cases, 19 African and Asian ancestry cases Illumina [10962468] (imputed) 6 ticagrelor measurement http://www.ebi.ac.uk/efo/EFO_0007007 GCST002882 Genome-wide genotyping array 2016-02-11 25935875 Varenhorst C 2015-05-02 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/25935875 Effect of genetic variations on ticagrelor plasma levels and clinical outcomes. AR-C124910XX levels in individuals with acute coronary syndromes treated with ticagrelor 1,794 European ancestry cases, 18 African and Asian ancestry cases 1,922 European ancestry cases, 19 African and Asian ancestry cases Illumina [10962468] (imputed) 2 AR-C124910XX measurement http://www.ebi.ac.uk/efo/EFO_0007020 GCST002883 Genome-wide genotyping array 2015-09-10 25917933 Zai CC 2014-11-20 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/25917933 A genome-wide association study of suicide severity scores in bipolar disorder. Suicide in bipolar disorder 959 European ancestry individuals NA Affymetrix, Illumina [2659407] (imputed) 4 suicide behaviour measurement, attempted suicide http://www.ebi.ac.uk/efo/EFO_0006882, http://www.ebi.ac.uk/efo/EFO_0004321 GCST002699 Genome-wide genotyping array 2016-02-04 25918995 Salvatore JE 2015-04-28 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25918995 Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior. Adult antisocial behavior 621 European ancestry individuals 498 European ancestry individuals from alcohol dependence affected families Illumina [7287851] (imputed) 0 antisocial behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007052 GCST002877 Genome-wide genotyping array 2013-01-31 23151678 Takata R 2012-11-15 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23151678 Impact of four loci on serum tamsulosin hydrochloride concentration. Serum tamsulosin hydrochloride concentration 182 Japanese ancestry individuals NA Illumina [481678] 4 response to tamsulosin http://purl.obolibrary.org/obo/GO_1901905 GCST001744 Genome-wide genotyping array 2015-08-01 25533513 Yao SL 2014-12-22 Chin J Integr Med www.ncbi.nlm.nih.gov/pubmed/25533513 Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study. Yang-deficiency constitution 30 cases, 30 balanced constitution controls NA Affymetrix [668548] 1 yang deficiency http://www.ebi.ac.uk/efo/EFO_0006817 GCST002728 Genome-wide genotyping array 2016-01-16 25839716 Ng E 2015-04-02 Environ Res www.ncbi.nlm.nih.gov/pubmed/25839716 Genome-wide association study of plasma levels of polychlorinated biphenyls disclose an association with the CYP2B6 gene in a population-based sample. Polychlorinated biphenyl levels 922 European ancestry individuals NA Illumina [8736858] (imputed) 57 polychlorinated biphenyls measurement http://www.ebi.ac.uk/efo/EFO_0007042 GCST002839 Genome-wide genotyping array 2016-06-15 25944848 Athanasiu L 2015-05-05 J Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/25944848 Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs. Pharmacokinetics of antidepressant drugs in severe mental disorder (concentration dose ratio) Up to 320 European ancestry cases NA Affymetrix [686595] 1 concentration dose ratio, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007635, http://purl.obolibrary.org/obo/GO_0036276 GCST002891 Genome-wide genotyping array 2016-06-15 25944848 Athanasiu L 2015-05-05 J Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/25944848 Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs. Pharmacokinetics of antiepileptic drugs in severe mental disorder (concentration drug ratio) Up to 185 European ancestry cases NA Affymetrix [686595] 4 concentration dose ratio, response to anticonvulsant http://www.ebi.ac.uk/efo/EFO_0007635, http://purl.obolibrary.org/obo/GO_0036277 GCST002887 Genome-wide genotyping array 2016-06-15 25944848 Athanasiu L 2015-05-05 J Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/25944848 Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs. Pharmacokinetics of antipsychotic drugs in severe mental disorder (concentration drug ratio) Up to 829 European ancestry cases NA Affymetrix [686595] 3 concentration dose ratio, response to antipsychotic drug http://www.ebi.ac.uk/efo/EFO_0007635, http://purl.obolibrary.org/obo/GO_0097332 GCST002888 Genome-wide genotyping array 2016-06-15 25944848 Athanasiu L 2015-05-05 J Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/25944848 Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs. Pharmacokinetics of olanzapine in severe mental disorder (concentration dose ratio) Up to 290 European ancestry cases NA Affymetrix [686595] 4 response to olanzapine, concentration dose ratio http://purl.obolibrary.org/obo/GO_0097333, http://www.ebi.ac.uk/efo/EFO_0007635 GCST002885 Genome-wide genotyping array 2015-11-21 25934476 de Vries PS 2015-05-01 Blood www.ncbi.nlm.nih.gov/pubmed/25934476 Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity. ADAMTS13 activity 3,423 European ancestry individuals 2,025 European ancestry individuals Illumina [8237900] (imputed) 4 ADAMTS13 activity measurement http://www.ebi.ac.uk/efo/EFO_0006955 GCST002881 Genome-wide genotyping array 2013-01-30 23166209 Smith JG 2012-11-19 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23166209 Impact of ancestry and common genetic variants on QT interval in African Americans. QT interval 13,105 African American individuals NA Affymetrix, Illumina [2800000] (imputed) 29 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST001746 Genome-wide genotyping array 2013-03-21 23291585 Fakiola M 2013-01-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23291585 Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis. Leishmaniasis (visceral) 989 Indian ancestry cases, 1,089 Indian ancestry controls, 357 Brazilian ancestry cases, 1,613 Brazilian ancestry unaffected relatives 951 Indian ancestry cases, 990 Indian ancestry controls Illumina [521134] 1 visceral Leishmaniasis http://www.ebi.ac.uk/efo/EFO_0005045 GCST001805 Genome-wide genotyping array 2015-04-17 25145502 Tang S 2014-08-22 Ann Surg Oncol www.ncbi.nlm.nih.gov/pubmed/25145502 Genome-wide association study of survival in early-stage non-small cell lung cancer. Non-small cell lung cancer (survival) 354 Han Chinese ancestry cases 327 Han Chinese ancestry cases Affymetrix [589102] 3 survival time, non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0003060 GCST002577 Genome-wide genotyping array 2014-03-27 24043878 Wong EH 2013-09-16 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/24043878 Common variants on Xq28 conferring risk of schizophrenia in Han Chinese. Schizophrenia 481 Han Chinese ancestry cases, 2,025 Han Chinese ancestry controls 1,088 Han Chinese ancestry cases, 1,063 Han Chinese ancestry controls Illumina [2383054] (imputed) 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST002190 Genome-wide genotyping array 2013-01-30 23144326 Kim DK 2012-11-09 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/23144326 Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease. Chronic obstructive pulmonary disease-related biomarkers Up to 1,951 European ancestry smokers NA Illumina [588352] 34 tumor necrosis factor-alpha measurement, interleukin-6 measurement, chronic obstructive pulmonary disease, interleukin-8 measurement, fibrinogen measurement, C-reactive protein measurement, CC16 measurement, surfactant protein D measurement http://www.ebi.ac.uk/efo/EFO_0004684, http://www.ebi.ac.uk/efo/EFO_0004810, http://www.ebi.ac.uk/efo/EFO_0000341, http://www.ebi.ac.uk/efo/EFO_0004811, http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0005080, http://www.ebi.ac.uk/efo/EFO_0005081 GCST001737 Genome-wide genotyping array 2014-01-22 23872634 Bezzina CR 2013-07-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23872634 Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Brugada syndrome 312 European ancestry cases, 1,115 European ancestry controls 594 European ancestry cases, 806 European ancestry controls, 208 Japanese ancestry cases, 1,1016 Japanese controls Affymetrix [360149] 3 Brugada syndrome http://purl.obolibrary.org/obo/MONDO_0015263 GCST002098 Genome-wide genotyping array 2014-03-15 23972371 Franceschini N 2013-08-20 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23972371 Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. Blood pressure 28,190 African American individuals, 1,188 Nigerian ancestry individuals 69,395 European ancestry individuals, 5,266 African American individuals, 6,497 African ancestry individuals, 19,601 East Asian ancestry individuals Affymetrix, Illumina [~ 2420000] (imputed) 11 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST002143 Genome-wide genotyping array 2013-02-13 23204130 Wheeler HE 2012-11-30 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/23204130 Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy. Paclitaxel-induced neuropathy 77 European ancestry lymphoblastoid cell lines, 87 Yoruban ancestry lymphoblastoid cell lines, 83 African American lymphoblastoid cell lines NA NR [> 2000000] (imputed) 0 methylcobalamin deficiency type cblE, neuropathy http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0004149 GCST001755 Genome-wide genotyping array 2008-09-25 18780872 Liu P 2008-09-17 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/18780872 Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. Lung cancer 194 European ancestry cases, 219 European ancestry controls 3,878 cases, 4,831 controls Affymetrix [up to 722376] 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000233 Genome-wide genotyping array 2013-05-11 23400010 Del-Aguila JL 2013-02-12 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/23400010 Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans. Thiazide-induced adverse metabolic effects in hypertensive patients 425 European ancestry cases, 342 African American cases NA Affymetrix, Illumina [> 2000000] (imputed) 59 response to hydrochlorothiazide, triglyceride measurement, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0005202, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004465 GCST001859 Genome-wide genotyping array 2015-02-06 24920014 Cozen W 2014-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24920014 A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus. Hodgkin's lymphoma 1,816 European ancestry cases, 7,877 European ancestry controls 1,281 European ancestry cases, 3,218 European ancestry controls Affymetrix, Illumina [1004829] (imputed) 7 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST002480 Genome-wide genotyping array 2012-12-11 23023329 Xu J 2012-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23023329 Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4. Prostate cancer 1,417 Han Chinese ancestry cases, 1,008 Han Chinese ancestry controls 3,067 Han Chinese ancestry cases, 7,926 Han Chinese ancestry controls Illumina [587294] 3 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001702 Genome-wide genotyping array 2014-10-17 24582949 Docampo E 2014-02-26 Pain www.ncbi.nlm.nih.gov/pubmed/24582949 Genome-wide analysis of single nucleotide polymorphisms and copy number variants in fibromyalgia suggest a role for the central nervous system. Fibromyalgia 300 European ancestry female cases, 203 European ancestry female controls 940 European ancestry female cases, 601 European ancestry female controls Illumina [505454] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST002370 Genome-wide genotyping array 2015-06-12 25317112 Oh S 2014-09-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/25317112 Epidemiological and genome-wide association study of gastritis or gastric ulcer in korean populations. Gastritis 977 Korean ancestry female cases, 3,622 Korean ancestry female controls, 804 Korean ancestry male cases, 3,335 Korean ancestry male controls NA NR [349184] 7 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST002638 Genome-wide genotyping array 2011-09-06 21846871 Mehta NN 2011-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/21846871 A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease. Coronary heart disease 8,424 European ancestry cases, 6,996 South Asian ancestry cases, 15,062 controls 21,408 cases, 19,185 controls Illumina [~ 57500] 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001185 Genome-wide genotyping array 2014-10-17 24578379 Huang J 2014-02-27 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/24578379 Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. Plasma plasminogen activator levels 26,217 European ancestry individuals, 712 Orcadian individuals 4,487 European ancestry individuals Affymetrix, Illumina [2455857] (imputed) 5 tissue plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0004791 GCST002374 Genome-wide genotyping array 2015-06-05 25226531 St Pourcain B 2014-09-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25226531 Common variation near ROBO2 is associated with expressive vocabulary in infancy. Expressive vocabulary in infants 6,851 European ancestry 15-18-month-old children, 6,299 European ancestry 24-30-month-old children 2,038 European ancestry 15-18-month-old children, 4,520 European ancestry 24-30-month-old children Illumina [2449665] (imputed) 8 infant expressive language ability http://www.ebi.ac.uk/efo/EFO_0006316 GCST002611 Genome-wide genotyping array 2018-11-08 24376627 Su WH 2013-12-23 PLoS One www.ncbi.nlm.nih.gov/pubmed/24376627 How genome-wide SNP-SNP interactions relate to nasopharyngeal carcinoma susceptibility. Nasopharyngeal carcinoma (SNP x SNP interaction) 277 Han Chinese ancestry cases, 285 Han Chinese ancestry controls 181 Han Chinese ancestry cases, 187 Han Chinese ancestry controls Illumina [480365] 41 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST006524 Genome-wide genotyping array 2016-01-31 25849990 Tapper W 2015-04-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25849990 Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms. Myeloproliferative neoplasms 524 European ancestry JAK2 negative cases, 2,674 European ancestry controls 1,383 European ancestry JAK2 negative cases, 4,609 European ancestry controls, 526 JAK2 negative cases, 5,506 controls Affymetrix [2098039] (imputed) 3 myeloproliferative disorder http://www.ebi.ac.uk/efo/EFO_0004251 GCST002840 Genome-wide genotyping array 2016-02-04 25918841 Sanchez-Juan P 2015-04-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/25918841 A genome wide association study links glutamate receptor pathway to sporadic Creutzfeldt-Jakob disease risk. Creutzfeldt-Jakob disease (sporadic) 434 European ancestry cases, 1,939 European ancestry controls 1,109 European ancestry cases, 2,264 European ancestry controls Affymetrix [279389] 2 sporadic Creutzfeld Jacob disease http://www.ebi.ac.uk/efo/EFO_1000656 GCST002878 Genome-wide genotyping array 2015-07-10 25434496 Kim S 2014-11-27 Gene www.ncbi.nlm.nih.gov/pubmed/25434496 Genetic variants at 1q32.1, 10q11.2 and 19q13.41 are associated with prostate-specific antigen for prostate cancer screening in two Korean population-based cohort studies. Prostate-specific antigen levels 554 Korean ancestry individuals 1,575 Korean ancestry individuals Affymetrix [2163106] (imputed) 5 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST002703 Genome-wide genotyping array 2016-02-04 25935106 Kim KW 2015-04-30 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/25935106 Genome-wide association study of recalcitrant atopic dermatitis in Korean children. Recalcitrant atopic dermatitis 246 Korean ancestry child cases, 551 Korean ancestry adult controls NA Affymetrix [2501352] (imputed) 5 recalcitrant atopic dermatitis http://www.ebi.ac.uk/efo/EFO_1000651 GCST002880 Genome-wide genotyping array 2016-02-07 25918132 Yucesoy B 2015-04-26 Toxicol Sci www.ncbi.nlm.nih.gov/pubmed/25918132 Genome-Wide Association Study Identifies Novel Loci Associated With Diisocyanate-Induced Occupational Asthma. Diisocyanate-induced asthma 74 European ancestry cases, 824 European ancestry controls NA Illumina [1556551] 180 asthma, response to diisocyanate http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0006995 GCST002875 Genome-wide genotyping array 2013-01-30 23160099 Justice CM 2012-11-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23160099 A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9. Sagittal craniosynostosis 130 European ancestry trios 172 cases, 548 controls Illumina [915307] 2 isolated scaphocephaly http://purl.obolibrary.org/obo/MONDO_0018112 GCST001745 Genome-wide genotyping array 2015-05-07 25162662 Liao M 2014-08-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/25162662 Genome-wide association study identifies variants in PMS1 associated with serum ferritin in a Chinese population. Ferritin levels 1,999 Han Chinese ancestry individuals 1,496 Chinese ancestry individuals Illumina [1940243] (imputed) 1 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST002578 Genome-wide genotyping array 2016-01-13 25710614 Hong X 2015-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25710614 Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children. Peanut allergy 316 European ancestry child cases, 144 European ancestry non-allergic non-sensitized normal child controls, 589 European ancestry uncertain phenotype child controls, 1,148 European ancestry uncertain phenotype adult controls 62 European ancestry child cases, 69 European ancestry child controls, 24 child cases, 58 child controls Illumina [6459842] (imputed) 3 peanut allergy measurement http://www.ebi.ac.uk/efo/EFO_0007017 GCST002791 Genome-wide genotyping array 2016-01-13 25710614 Hong X 2015-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25710614 Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children. Milk allergy 291 European ancestry child cases, 144 European ancestry non-allergic non-sensitized normal child controls, 614 European ancestry uncertain phenotype child controls, 1,148 European ancestry uncertain phenotype adult controls NA Illumina [6459842] (imputed) 5 milk allergy measurement http://www.ebi.ac.uk/efo/EFO_0007019 GCST002788 Genome-wide genotyping array 2016-01-13 25710614 Hong X 2015-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25710614 Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children. Egg allergy 217 European ancestry child cases, 144 European ancestry non-allergic non-sensitized normal child controls, 688 European ancestry uncertain phenotype child controls, 1,148 European ancestry uncertain phenotype adult controls NA Illumina [6459842] (imputed) 5 egg allergy measurement http://www.ebi.ac.uk/efo/EFO_0007018 GCST002789 Genome-wide genotyping array 2016-01-13 25710614 Hong X 2015-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25710614 Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children. Food allergy 671 European ancestry child cases, 144 European ancestry non-allergic non-sensitized child controls, 234 European ancestry uncertain phenotype child controls, 1,148 European ancestry uncertain phenotype adult controls NA Illumina [6459842] (imputed) 5 food allergy measurement http://www.ebi.ac.uk/efo/EFO_0007016 GCST002790 Genome-wide genotyping array 2012-12-10 22981920 Weissflog L 2012-09-13 Eur Neuropsychopharmacol www.ncbi.nlm.nih.gov/pubmed/22981920 KCNIP4 as a candidate gene for personality disorders and adult ADHD. Personality disorders 200 European ancestry Cluster B personality disorder cases, 200 European ancestry Cluster C cases, 600 European ancestry controls NA Affymetrix [488634] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST001682 Genome-wide genotyping array 2015-08-13 25488688 Pino-Yanes M 2014-12-06 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/25488688 Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos. Serum IgE levels 1,854 Hispanic asthmatic individuals, 1,480 Hispanic individuals 454 Hispanic asthmatic individuals Affymetrix [723888] 2 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST002717 Genome-wide genotyping array 2016-02-11 25914168 Esposito F 2015-05-14 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/25914168 A pharmacogenetic study implicates SLC9a9 in multiple sclerosis disease activity. Response to interferon beta in multiple sclerosis 74 European ancestry responders, 42 European ancestry non-responders 346 European ancestry responders, 254 European ancestry non-responders, 137 responders, 144 non-responders Illumina [539016] 0 response to interferon-beta http://purl.obolibrary.org/obo/GO_0035456 GCST002910 Genome-wide genotyping array 2013-01-23 23137000 Lin HJ 2012-11-09 Ophthalmic Genet www.ncbi.nlm.nih.gov/pubmed/23137000 Novel susceptibility genes associated with diabetic cataract in a Taiwanese population. Cataracts in type 2 diabetes 109 Han Chinese ancestry cases, 649 Han Chinese ancestry controls NA Illumina [517401] 2 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST001736 Genome-wide genotyping array 2014-06-26 20421936 Scherag A 2010-04-22 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20421936 Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups. Obesity (early onset extreme) 1,138 European ancestry cases, 1,120 European ancestry normal or lean controls 1,181 European ancestry cases, 1,960 European ancestry normal or lean controls, 981 European ancestry cases and 1,430 European ancestry controls from 715 families Affymetrix, Illumina [1596878] (imputed) 5 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST000663 Genome-wide genotyping array 2014-10-21 24578207 Opherk C 2014-02-27 Stroke www.ncbi.nlm.nih.gov/pubmed/24578207 Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL. White matter hyperintensity volume in cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy 466 European ancestry individuals NA Affymetrix [583499] 4 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST002377 Genome-wide genotyping array 2014-04-09 24086445 Wang Q 2013-09-24 PLoS One www.ncbi.nlm.nih.gov/pubmed/24086445 Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-naïve patients with schizophrenia. Gray matter volume (schizophrenia interaction) 74 Han Chinese ancestry cases, 51 Han Chinese ancestry controls NA NR [1983054] (imputed) 3 schizophrenia, grey matter volume measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0005420 GCST002203 Genome-wide genotyping array 2019-01-10 24325914 Chu M 2013-12-09 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/24325914 A genome-wide gene-gene interaction analysis identifies an epistatic gene pair for lung cancer susceptibility in Han Chinese. Lung cancer (SNP x SNP interaction) 2,331 Han Chinese ancestry cases, 3,077 Han Chinese ancestry controls 4,046 Han Chinese ancestry cases, 3,938 Han Chinese ancestry controls Affymetrix [591370] 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST006866 Genome-wide genotyping array 2015-06-14 25352340 Benyamin B 2014-10-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25352340 Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Iron status biomarkers (ferritin levels) 23,986 European ancestry individuals Up to 24,986 European ancestry individuals Affymetrix, Illumina [~ 2100000] (imputed) 5 iron biomarker measurement, ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004461, http://www.ebi.ac.uk/efo/EFO_0004459 GCST002677 Genome-wide genotyping array 2015-06-14 25352340 Benyamin B 2014-10-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25352340 Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Iron status biomarkers (transferrin saturation) 23,986 European ancestry individuals Up to 24,986 European ancestry individuals Affymetrix, Illumina [~ 2100000] (imputed) 6 iron biomarker measurement, transferrin saturation measurement http://www.ebi.ac.uk/efo/EFO_0004461, http://www.ebi.ac.uk/efo/EFO_0006333 GCST002680 Genome-wide genotyping array 2015-06-14 25352340 Benyamin B 2014-10-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25352340 Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Iron status biomarkers (iron levels) 23,986 European ancestry individuals Up to 24,986 European ancestry individuals Affymetrix, Illumina [~ 2100000] (imputed) 5 iron biomarker measurement, serum iron measurement http://www.ebi.ac.uk/efo/EFO_0004461, http://www.ebi.ac.uk/efo/EFO_0006332 GCST002679 Genome-wide genotyping array 2015-06-14 25352340 Benyamin B 2014-10-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25352340 Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis. Iron status biomarkers (transferrin levels) 23,986 European ancestry individuals Up to 24,986 European ancestry individuals Affymetrix, Illumina [~ 2100000] (imputed) 9 iron biomarker measurement, transferrin measurement http://www.ebi.ac.uk/efo/EFO_0004461, http://www.ebi.ac.uk/efo/EFO_0006341 GCST002678 Genome-wide genotyping array 2015-05-29 25256105 Freitag-Wolf S 2014-09-25 J Clin Periodontol www.ncbi.nlm.nih.gov/pubmed/25256105 Genome-wide exploration identifies sex-specific genetic effects of alleles upstream NPY to increase the risk of severe periodontitis in men. Aggressive periodontitis (sex interaction) 329 European ancestry cases, 983 European ancestry controls 382 European ancestry cases, 489 European ancestry controls Affymetrix [287224] 1 sex interaction measurement, aggressive periodontitis http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0006342 GCST002635 Genome-wide genotyping array 2014-08-01 24376798 Miki D 2013-12-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24376798 HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study. Chronic hepatitis C infection 481 Japanese ancestry cases, 2,963 Japanese ancestry controls 5,737 Japanese ancestry cases, 26,931 Japanese ancestry controls Illumina [458207] 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST002316 Genome-wide genotyping array 2014-10-21 24603532 Nongpiur ME 2014-03-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24603532 ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma. Anterior chamber depth 1,752 Malay ancestry individuals, 1,860 Indian ancestry individuals, 872 Chinese ancestry individuals 824 Chinese ancestry individuals Illumina [NR] 1 anterior chamber depth measurement http://www.ebi.ac.uk/efo/EFO_0005668 GCST002383 Genome-wide genotyping array 2014-04-16 24123702 Chung CM 2014-03-03 Diabetes Metab Res Rev www.ncbi.nlm.nih.gov/pubmed/24123702 Common quantitative trait locus downstream of RETN gene identified by genome-wide association study is associated with risk of type 2 diabetes mellitus in Han Chinese: a Mendelian randomization effect. Resistin levels 382 Han Chinese ancestry indiviudals 559 Han Chinese ancestry indiviudals Illumina [NR] 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST002381 Genome-wide genotyping array 2015-04-23 25108386 Hou S 2014-08-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25108386 Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3. Vogt-Koyanagi-Harada syndrome 774 Han Chinese ancestry cases, 2,009 Han Chinese ancestry controls 764 Han Chinese ancestry cases, 3594 Han Chinese ancestry controls Affymetrix, Illumina [2208258] (imputed) 4 Vogt-Koyanagi-Harada disease http://purl.obolibrary.org/obo/MONDO_0018092 GCST002562 Genome-wide genotyping array 2015-04-01 24962563 Rubicz R 2014-07-01 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/24962563 Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens. Food antigen IgG levels 1,367 Mexican Americans from 63 families NA Illumina [944565] (imputed) 7 serum IgG measurement, response to dietary antigen http://www.ebi.ac.uk/efo/EFO_0004565, http://www.ebi.ac.uk/efo/EFO_0005844 GCST002518 Genome-wide genotyping array 2015-06-27 25411281 Dashti HS 2014-10-08 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/25411281 Meta-analysis of genome-wide association studies for circulating phylloquinone concentrations. Circulating phylloquinone levels 2,138 European ancestry individuals NA Affymetrix, Illumina [2543887] (imputed) 5 vitamin K measurement http://www.ebi.ac.uk/efo/EFO_0004618 GCST002653 Genome-wide genotyping array 2015-06-27 25271088 Singh A 2014-10-01 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25271088 Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene. Hip circumference (psychosocial stress interaction) 2,460 European ancestry individuals, 548 Chinese ancestry individuals, 1,547 African American individuals, 1,250 Hispanic individuals 3,157 European ancestry individuals Affymetrix [528298] 5 hip circumference, psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0005093, http://www.ebi.ac.uk/efo/EFO_0006783 GCST002641 Genome-wide genotyping array 2015-04-15 25109461 Ollila HM 2014-08-11 J Sleep Res www.ncbi.nlm.nih.gov/pubmed/25109461 Genome-wide association study of sleep duration in the Finnish population. Sleep duration 1,941 European ancestry individuals 6,834 European ancestry individuals Illumina [555388] 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST002565 Genome-wide genotyping array 2015-04-23 25117820 Schneider BP 2014-08-12 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/25117820 Genetic variant predicts bevacizumab-induced hypertension in ECOG-5103 and ECOG-2100. Response to chemotherapy in breast cancer (hypertension) (bevacizumab) 255 European ancestry cases, 387 European ancestry controls Illumina [up to 810372] (imputed) 3 response to bevacizumab, chemotherapy-induced hypertension http://www.ebi.ac.uk/efo/EFO_0005943, http://www.ebi.ac.uk/efo/EFO_0005942 GCST002567 Genome-wide genotyping array 2015-04-23 25117820 Schneider BP 2014-08-12 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/25117820 Genetic variant predicts bevacizumab-induced hypertension in ECOG-5103 and ECOG-2100. Response to chemotherapy in breast cancer hypertensive cases (cumulative dose) (bevacizumab) 255 European ancestry cases, 387 European ancestry controls Illumina [up to 810372] (imputed) 13 cumulative dose response to bevacizumab http://www.ebi.ac.uk/efo/EFO_0005944 GCST002566 Genome-wide genotyping array 2015-04-01 25038754 Cai Q 2014-07-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25038754 Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1. Breast cancer 2,867 Chinese ancestry cases, 2,285 Chinese ancestry controls, 2,246 Korean ancestry cases, 2,052 Korean ancestry controls 5,029 Chinese ancestry cases, 5,302 Chinese ancestry controls, 6,066 Korean ancestry cases, 8,003 Korean ancestry controls, 6,572 Japanese ancestry cases, 6,539 Japanese ancestry controls, 16,003 European ancestry cases, 41,335 European ancestry controls Affymetrix [up to 1930412] (imputed) 4 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST002537 Genome-wide genotyping array 2015-06-23 25237182 Erickson SW 2014-09-18 Blood www.ncbi.nlm.nih.gov/pubmed/25237182 Genome-wide scan identifies variant in 2q12.3 associated with risk for multiple myeloma. Multiple myeloma 972 European ancestry cases, 1,064 European ancestry controls NA Illumina [777681] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST002614 Genome-wide genotyping array 2015-09-15 25387708 Vaidyanathan U 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387708 Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: a genome-wide association study. Acoustic startle blink response 3,323 European ancestry twins and their parents NA Illumina [527829] 6 acoustic startle blink response measurement http://www.ebi.ac.uk/efo/EFO_0006875 GCST002708 Genome-wide genotyping array 2015-01-21 24974787 Meng W 2014-06-26 Eur J Pain www.ncbi.nlm.nih.gov/pubmed/24974787 A genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain. Neuropathic pain in type 2 diabetes 572 European ancestry cases, 2,491 European ancestry controls NA Affymetrix, Illumina [6494962] (imputed) 2 neuropathic pain http://www.ebi.ac.uk/efo/EFO_0005762 GCST002507 Genome-wide genotyping array 2011-09-27 21873549 Strawbridge RJ 2011-08-26 Diabetes www.ncbi.nlm.nih.gov/pubmed/21873549 Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Proinsulin levels 10,701 European ancestry individuals 16,378 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 10 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST001212 Genome-wide genotyping array 2011-09-27 21876473 Lydall GJ 2011-08-26 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21876473 Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder. Alcohol dependence 506 European ancestry cases, 510 European ancestry controls NA Affymetrix [372193] 1 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001211 Genome-wide genotyping array 2010-11-03 20920776 DeWan AT 2010-10-01 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/20920776 PDE11A associations with asthma: results of a genome-wide association scan. Asthma 28 European ancestry child cases, 19 European ancestry child controls, 11 African American child cases, 4 African American child controls, 18 Hispanic child cases, 14 Hispanic child controls, 9 Biracial child cases, 5 Biracial child controls 18 European ancestry child cases, 367 European ancestry child controls, 1 African American child cases, 28 African American child controls, 6 Hispanic child cases, 28 Hispanic child controls, 13 Biracial child cases, 38 Biracial child controls Affymetrix [396207] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000819 Genome-wide genotyping array 2015-01-21 24950379 Metrustry SJ 2014-06-20 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/24950379 Variants close to NTRK2 gene are associated with birth weight in female twins. Birth weight 4,593 European ancestry female twins 3,033 European ancestry female twins, 1,418 European ancestry females, 1,579 European ancestry males Illumina [up to 874733] 1 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST002499 Genome-wide genotyping array 2014-10-23 24680774 Mezzavilla M 2014-03-25 Gene www.ncbi.nlm.nih.gov/pubmed/24680774 Insight into genetic determinants of resting heart rate. Resting heart rate 855 Friuli Venezia Giulia (founder/genetic isolate) individuals NA Illumina [2058182] (imputed) 2 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST002398 Genome-wide genotyping array 2011-08-15 21761138 Peters U 2011-07-15 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21761138 Meta-analysis of new genome-wide association studies of colorectal cancer risk. Colorectal cancer 2,906 European ancestry cases, 3,416 European ancestry controls 8,161 European ancestry cases, 9,101 European ancestry controls Illumina [378739] 5 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST001161 Genome-wide genotyping array 2016-12-01 26910538 Choi SH 2016-02-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26910538 Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies. Vascular endothelial growth factor levels 9541 European ancestry individuals, 1,115 Cilento (founder/genetic isolated) individuals, 897 Ogliastran (founder/genetic isolated) individuals, 1,759 Val Borbera (founder/genetic isolated) individuals 2,141 European ancestry individuals, 659 Sorbian (founder/genetic isolated) individuals Affymetrix, Illumina [6705861] (imputed) 10 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST003403 Genome-wide genotyping array 2013-05-26 23406873 Shi Y 2013-02-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23406873 A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population. Myopia (pathological) 665 Han Chinese ancestry cases, 960 Han Chinese ancestry controls 2,128 Han Chinese ancestry cases, 3,683 Han Chinese ancestry controls Illumina [286031] 5 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST001881 Genome-wide genotyping array 2014-07-30 24379826 Voruganti VS 2013-12-16 Front Genet www.ncbi.nlm.nih.gov/pubmed/24379826 Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans. Serum uric acid levels 632 Mexican American individuals NA Illumina [NR] (imputed) 2 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST002311 Genome-wide genotyping array 2016-02-04 25936594 Tomer Y 2015-04-27 J Autoimmun www.ncbi.nlm.nih.gov/pubmed/25936594 Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes. Type 1 diabetes and autoimmune thyroid diseases 346 European ancestry cases, 727 European ancestry controls 185 European ancestry cases, 340 European ancestry controls Illumina [514008] 11 autoimmune thyroid disease, type 1 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0006812, http://purl.obolibrary.org/obo/MONDO_0005147 GCST002876 Genome-wide genotyping array 2015-12-18 25663231 Beecham GW 2015-02-06 Neurology www.ncbi.nlm.nih.gov/pubmed/25663231 PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease. Parkinson disease and lewy body pathology 484 European ancestry cases, 1,145 European ancestry controls NA Illumina [3922209] (imputed) 10 Lewy body measurement, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0007021, http://purl.obolibrary.org/obo/MONDO_0005180 GCST002778 Genome-wide genotyping array 2015-11-17 25656473 de With SA 2015-02-05 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/25656473 Genome-wide association study of lymphoblast cell viability after clozapine exposure. Clozapine-induced cytotoxicity 90 European ancestry lymphoblast cell lines NA NR [2092490] 18 cytotoxicity measurement, response to clozapine http://www.ebi.ac.uk/efo/EFO_0006952, http://purl.obolibrary.org/obo/GO_0097338 GCST002777 Genome-wide genotyping array 2015-11-07 25672891 Shimizu S 2015-02-11 J Dent Res www.ncbi.nlm.nih.gov/pubmed/25672891 A genome-wide association study of periodontitis in a Japanese population. Periodontitis 1,593 Japanese ancestry cases, 7,980 Japanese ancestry controls 1,167 Japanese ancestry cases, 7,178 Japanese ancestry controls Illumina [597434] 2 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST002781 Genome-wide genotyping array 2015-11-17 25705849 Jacobs LC 2015-02-23 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/25705849 A Genome-Wide Association Study Identifies the Skin Color Genes IRF4, MC1R, ASIP, and BNC2 Influencing Facial Pigmented Spots. Facial pigmentation 2,844 European ancestry individuals NA Illumina [6846125] (imputed) 4 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST002785 Genome-wide genotyping array 2015-11-07 25629512 Cheng CY 2015-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25629512 New loci and coding variants confer risk for age-related macular degeneration in East Asians. Exudative age-related macular degeneration 2,119 East Asian ancestry cases, 5,691 East Asian ancestry controls 4,226 East Asian ancestry cases, 10,289 East Asian ancestry controls Illumina [4471719] (imputed) 7 wet macular degeneration http://www.ebi.ac.uk/efo/EFO_0004683 GCST002766 Genome-wide genotyping array 2016-01-12 25649651 Wang X 2015-02-03 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/25649651 Genetic Determinants of Survival in Patientswith Alzheimer’s Disease. Alzheimer's disease (survival time) 983 cases NA Illumina [803323] 7 Alzheimer disease, survival time http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0000714 GCST002775 Genome-wide genotyping array 2016-01-14 25643325 Renton AE 2015-04-01 JAMA Neurol www.ncbi.nlm.nih.gov/pubmed/25643325 A genome-wide association study of myasthenia gravis. Myasthenia gravis 972 European ancestry cases, 1,977 European ancestry controls 423 European ancestry cases, 467 European ancestry controls Illumina [8114394] (imputed) 3 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST002838 Genome-wide genotyping array 2015-11-12 25826619 Henrion MY 2015-03-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/25826619 Common variation at 1q24.1 (ALDH9A1) is a potential risk factor for renal cancer. Renal cell carcinoma 2,215 Western European ancestry cases, 8,566 Western European ancestry controls 2,844 European ancestry cases, 7,270 European ancestry controls Illumina [up to 12182133] (imputed) 3 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST002835 Genome-wide genotyping array 2017-01-27 27098658 Muller-Calleja N 2016-04-21 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/27098658 Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expression. Presence of antiphospholipid antibodies 4,163 German ancestry individuals NA Affymetrix [at least 662405] 12 antiphospholipid antibody measurement http://www.ebi.ac.uk/efo/EFO_0005200 GCST003563 Genome-wide genotyping array 2017-02-24 27225129 Okbay A 2016-05-26 Nature www.ncbi.nlm.nih.gov/pubmed/27225129 Genome-wide association study identifies 74 loci associated with educational attainment. Educational attainment (years of education) 405,072 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 9300000] (imputed) 162 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST003676 Genome-wide genotyping array 2017-02-25 27225129 Okbay A 2016-05-26 Nature www.ncbi.nlm.nih.gov/pubmed/27225129 Genome-wide association study identifies 74 loci associated with educational attainment. Educational attainment (college completion) 280,007 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 9300000] (imputed) 34 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST003677 Genome-wide genotyping array 2017-05-12 27997041 Traylor M 2016-12-20 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/27997041 Genetic variation at 16q24.2 is associated with small vessel stroke. Ischemic stroke 10,210 European ancestry cases, 12,285 European ancestry controls 7,743 European ancestry cases, 17,970 European ancestry controls Affymetrix, Illumina [NR] (imputed) 7 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST004023 Genome-wide genotyping array 2017-05-12 27997041 Traylor M 2016-12-20 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/27997041 Genetic variation at 16q24.2 is associated with small vessel stroke. Ischemic stroke (cardioembolic) 1,715 European ancestry cases, 12,285 European ancestry controls 3,101 European ancestry cases, 38,443 European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST004021 Genome-wide genotyping array 2017-05-12 27997041 Traylor M 2016-12-20 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/27997041 Genetic variation at 16q24.2 is associated with small vessel stroke. Small vessel stroke 2,275 European ancestry cases, 12,285 European ancestry controls 1,928 European ancestry cases, 38,443 European ancestry controls Affymetrix, Illumina [NR] (imputed) 1 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST004020 Genome-wide genotyping array 2017-05-12 27997041 Traylor M 2016-12-20 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/27997041 Genetic variation at 16q24.2 is associated with small vessel stroke. Large artery stroke 1,877 European ancestry cases, 12,285 European ancestry controls 1,130 European ancestry cases, 17,970 European ancestry controls Affymetrix, Illumina [NR] (imputed) 5 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST004022 Genome-wide genotyping array 2017-06-12 28282560 Pott J 2017-02-24 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/28282560 Genome-wide meta-analysis identifies novel loci of plaque burden in carotid artery. Carotid plaque burden 7,189 European ancestry individuals NA Affymetrix [9576485] (imputed) 39 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST004162 Genome-wide genotyping array 2017-05-11 27890468 van Hulzen KJE 2016-10-18 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27890468 Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. Bipolar disorder (age of onset <21) or attention deficit hyperactivity disorder 5,167 European ancestry bipolar disorder cases, 2,950 European ancestry ADHD cases, 1,659 European and unknown ancestry ADHD cases, 16,325 European ancestry controls, 2,942 European and unknown ancestry controls, 2,096 controls NA Affymetrix, Illumina [NR] 6 attention deficit hyperactivity disorder, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0004985 GCST004002 Genome-wide genotyping array 2017-05-11 27890468 van Hulzen KJE 2016-10-18 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27890468 Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis. Bipolar disorder or attention deficit hyperactivity disorder 9,650 European ancestry bipolar disorder cases, 2,950 European ancestry ADHD cases, 1,659 European and unknown ancestry ADHD cases, 16,325 European ancestry controls, 2,942 European and unknown ancestry controls, 2,096 controls NA Affymetrix, Illumina [NR] (imputed) 15 attention deficit hyperactivity disorder, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0004985 GCST004001 Genome-wide genotyping array 2017-06-01 28155865 Chen H 2017-02-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28155865 A Genome-Wide Association Study Identifies Genetic Variants Associated with Mathematics Ability. Mathematical ability 998 Han Chinese ancestry children 599 Han Chinese ancestry children Affymetrix [at least 1108437] 4 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST004123 Genome-wide genotyping array 2017-05-26 28223688 Bjornsdottir G 2017-02-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28223688 Sequence variant at 8q24.21 associates with sciatica caused by lumbar disc herniation. Sciatica caused by lumbar disc herniation (treated with microdiscectomy) 3,097 Icelandic ancestry cases, 1,651 non-array typed, familial imputed Icelandic ancestry cases, 132,966 Icelandic ancestry controls, 149,624 non-array typed, familial imputed Icelandic ancestry controls NR Illumina [21568490] (imputed) 1 lumbar disc herniation, Sciatica, LDH-related sciatica symptom severity measurement http://www.ebi.ac.uk/efo/EFO_1002005, http://purl.obolibrary.org/obo/HP_0011868, http://www.ebi.ac.uk/efo/EFO_0007941 GCST004098 Genome-wide genotyping array 2017-06-15 28193307 Lin BD 2017-02-14 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/28193307 Heritability and GWAS Studies for Monocyte-Lymphocyte Ratio. Monocyte-lymphocyte ratio 5,892 Dutch ancestry individuals NA Affymetrix, Illumina, Perlegen [5987253] (imputed) 3 monocyte:lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0007956 GCST004170 Genome-wide genotyping array 2017-06-12 28193307 Lin BD 2017-02-14 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/28193307 Heritability and GWAS Studies for Monocyte-Lymphocyte Ratio. Monocyte count 5,892 Dutch ancestry individuals NA Affymetrix, Illumina, Perlegen [5987253] (imputed) 5 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST004164 Genome-wide genotyping array 2018-04-26 26974007 Ellinghaus D 2016-03-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/26974007 Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. Chronic inflammatory diseases (ankylosing spondylitis, Crohn's disease, psoriasis, primary sclerosing cholangitis, ulcerative colitis) (pleiotropy) 8,726 European ancestry ankylosing spondylitis cases, 19,085 European ancestry Crohn’s disease cases, 6,530 European ancestry psoriasis cases, 3,408 European ancestry primary sclerosing cholangitis cases, 14,513 European ancestry ulcerative colitis cases, 34,213 European ancestry controls NA Illumina [130052] 244 ankylosing spondylitis, psoriasis, ulcerative colitis, Crohn's disease, sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0003898, http://www.ebi.ac.uk/efo/EFO_0000676, http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0000384, http://www.ebi.ac.uk/efo/EFO_0004268 GCST005537 Targeted genotyping array [ImmunoChip] 2017-05-11 28017375 van Rooij FJA 2016-12-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28017375 Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. Mean corpuscular volume up to 29,946 European ancestry individuals, up to 6150 African American individuals, 15,074 East Asian individuals. 16,389 individuals of European and African American ancestry. NR [2500000] (imputed) 58 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST004004 Genome-wide genotyping array 2017-05-11 28017375 van Rooij FJA 2016-12-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28017375 Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. Hemoglobin levels up to 40,258 European ancestry individuals, 16,128 African American individuals, up to 15,252 East Asian ancestry individuals. 16,389 European and African American individuals Affymetrix, Illumina [2500000] (imputed) 14 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST004005 Genome-wide genotyping array 2017-05-11 28017375 van Rooij FJA 2016-12-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28017375 Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. Mean corpuscular hemoglobin concentration up to 21,020 European ancestry individuals, up to 3,621 African American individuals, up to 15,062 East Asian individuals. 16,389 European and African American individuals. NR [2500000] (imputed) 20 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST004007 Genome-wide genotyping array 2017-05-11 28017375 van Rooij FJA 2016-12-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28017375 Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. Red blood cell count up to 40,258 European ancestry individuals, up to 16,128 African American individuals, up to 15,252 East Asian individuals. 16,389 individuals of European and African American ancestry. NR [2500000] (imputed) 20 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST004008 Genome-wide genotyping array 2017-05-11 28017375 van Rooij FJA 2016-12-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28017375 Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. Mean corpuscular hemoglobin up to 21,020 European ancestry individuals, up to 3,621 African American individuals, up to 15,062 East Asian individuals. 16,389 individuals of European and African American ancestry. NR [2500000] (imputed) 39 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST004006 Genome-wide genotyping array 2017-05-11 28017375 van Rooij FJA 2016-12-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28017375 Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis. Hematocrit up to 40,258 European ancestry individuals, up to 16,128 African American individuals, up to 15,252 East Asian ancestry individuals. 16,389 European and African American individuals NR [2500000] (imputed) 15 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST004003 Genome-wide genotyping array 2017-07-13 28298293 Hu Y 2017-03-15 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28298293 Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. Palmitoleic acid (16:1n-7) levels 3,521 Chinese ancestry individuals, European individuals (see Wu 2013). NA Affymetrix, Illumina [~ 2200000] (imputed) 4 palmitoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0007973 GCST004339 Genome-wide genotyping array 2017-07-13 28298293 Hu Y 2017-03-15 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28298293 Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. Vaccenic acid (18:1n-7) levels 3,521 Chinese ancestry individuals, 12,020 European ancestry individuals NA Affymetrix, Illumina [2200000] (imputed) 4 vaccenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007974 GCST004342 Genome-wide genotyping array 2017-07-13 28298293 Hu Y 2017-03-15 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28298293 Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. Oleic acid (18:1n-9) levels 3,521 Chinese ancestry individuals, European ancestry individuals (see Wu et al 2013) NA Affymetrix, Illumina [2200000] (imputed) 4 oleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006810 GCST004338 Genome-wide genotyping array 2017-07-13 28298293 Hu Y 2017-03-15 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28298293 Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. Gondoic acid (20:1n-9) levels 3,521 Chinese ancestry individuals, 12,020 European ancestry individuals NA Affymetrix, Illumina [2200000] (imputed) 4 gondoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007975 GCST004337 Genome-wide genotyping array 2017-07-13 28298293 Hu Y 2017-03-15 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28298293 Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. Erucic acid (22:1n-9) levels 3,521 Chinese ancestry individuals, 12,020 European ancestry individuals NA Affymetrix, Illumina [2200000] (imputed) 0 erucic acid measurement http://www.ebi.ac.uk/efo/EFO_0007976 GCST004340 Genome-wide genotyping array 2017-07-13 28298293 Hu Y 2017-03-15 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/28298293 Discovery and fine-mapping of loci associated with MUFAs through trans-ethnic meta-analysis in Chinese and European populations. Nervonic acid (24:1n-9) levels 3,521 Chinese ancestry individuals, 12,020 European ancestry individuals NA Affymetrix, Illumina [2200000] (imputed) 0 nervonic acid measurement http://www.ebi.ac.uk/efo/EFO_0007977 GCST004341 Genome-wide genotyping array 2017-06-01 28177523 Lin Y 2017-02-22 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/28177523 Association between genetic variation within vitamin D receptor-DNA binding sites and risk of basal cell carcinoma. Basal cell carcinoma 17,187 European ancestry cases, 287,054 European ancestry controls NA Affymetrix, Illumina [8262488] (imputed) 2 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST004113 Genome-wide genotyping array 2017-06-06 28273873 Park YM 2017-03-05 Nutrients www.ncbi.nlm.nih.gov/pubmed/28273873 Interaction between Single Nucleotide Polymorphism and Urinary Sodium, Potassium, and Sodium-Potassium Ratio on the Risk of Hypertension in Korean Adults. Hypertension 8,839 Korean ancestry individuals. NA Affymetrix [1291657] (imputed) 3 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST004143 Genome-wide genotyping array 2017-05-11 28317148 Campo C 2017-01-01 Hematol Oncol www.ncbi.nlm.nih.gov/pubmed/28317148 Bortezomib-induced peripheral neuropathy: A genome-wide association study on multiple myeloma patients. Bortezomib-induced peripheral neuropathy in multiple myeloma 102 European ancestry cases and 544 European ancestry controls. NR Illumina [NR] (imputed) 4 peripheral neuropathy, response to bortezomib http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0007808 GCST003964 Genome-wide genotyping array 2017-04-20 28012008 Lu S 2016-12-23 J Bone Miner Metab www.ncbi.nlm.nih.gov/pubmed/28012008 Bivariate genome-wide association analyses identified genetic pleiotropic effects for bone mineral density and alcohol drinking in Caucasians. Whole body bone mineral density and alcohol drinking 506 European ancestry males, 1,553 European ancestry females NA Affymetrix [69108] 0 alcohol consumption measurement, bone density http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0003923 GCST003921 Genome-wide genotyping array 2017-04-20 28012008 Lu S 2016-12-23 J Bone Miner Metab www.ncbi.nlm.nih.gov/pubmed/28012008 Bivariate genome-wide association analyses identified genetic pleiotropic effects for bone mineral density and alcohol drinking in Caucasians. Hip bone mineral density and alcohol drinking 506 European ancestry males, 1,553 European ancestry females NA Affymetrix [69108] 0 hip bone mineral density, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007702, http://www.ebi.ac.uk/efo/EFO_0007878 GCST003920 Genome-wide genotyping array 2017-04-20 28012008 Lu S 2016-12-23 J Bone Miner Metab www.ncbi.nlm.nih.gov/pubmed/28012008 Bivariate genome-wide association analyses identified genetic pleiotropic effects for bone mineral density and alcohol drinking in Caucasians. Spine bone mineral density and alcohol drinking 506 European ancestry males, 1,553 European ancestry females NA Affymetrix [69108] 1 alcohol consumption measurement, spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0007701 GCST003919 Genome-wide genotyping array 2017-06-20 28274756 Mhatre S 2017-03-03 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/28274756 Common genetic variation and risk of gallbladder cancer in India: a case-control genome-wide association study. Gallbladder cancer 1,042 Indian ancestry cases, 1,709 Indian ancestry controls 428 Indian ancestry cases, 420 Indian ancestry controls Illumina [10400000] (imputed) 2 gallbladder neoplasm http://www.ebi.ac.uk/efo/EFO_0004606 GCST004201 Genome-wide genotyping array 2017-05-30 28167095 Forno E 2017-02-04 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/28167095 Genome-wide interaction study of dust mite allergen on lung function in children with asthma. Lung function (FEV1/FVC) in asthma (dust mite allergen exposure interaction) 440 Puerto Rican ancestry child cases 497 European ancestry child cases, 605 Hispanic child cases Illumina [1830000] (imputed) 2 allergen exposure measurement, FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0007944, http://www.ebi.ac.uk/efo/EFO_0004713 GCST004108 Genome-wide genotyping array 2017-05-30 28167095 Forno E 2017-02-04 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/28167095 Genome-wide interaction study of dust mite allergen on lung function in children with asthma. Lung function (FEV1) in asthma (dust mite allergen exposure interaction) 440 Puerto Rican ancestry child cases 497 European ancestry child cases, 605 Hispanic child cases Illumina [1830000] (imputed) 5 forced expiratory volume, allergen exposure measurement http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0007944 GCST004107 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Parkinson's disease 9,619 European ancestry cases, 324,522 European ancestry controls NA Illumina [12438219] (imputed) 25 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST003984 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Breast size 33,790 European ancestry individuals NA Illumina [12039487] (imputed) 23 breast size http://www.ebi.ac.uk/efo/EFO_0004884 GCST003985 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Migraine 53,109 European ancestry cases, 230,876 European ancestry controls NA Illumina [13763073] (imputed) 27 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST003986 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Asthma 28,399 European ancestry cases, 128,843 European ancestry controls NA Illumina [13747813] (imputed) 27 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST003987 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Hypothyroidism 17,558 European ancestry cases, 117,083 European ancestry controls NA Illumina [13676411] (imputed) 26 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST003988 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Chin dimples 58,032 European ancestry cases, 13,457 European ancestry controls NA Illumina [13537761] (imputed) 46 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST003989 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Allergy 66,973 European ancestry cases, 113,768 European ancestry controls NA Illumina [12845910] (imputed) 26 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST003990 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Childhood ear infection 46,936 European ancestry cases, 74,874 European ancestry controls NA Illumina [13754664] (imputed) 24 susceptibility to childhood ear infection measurement http://www.ebi.ac.uk/efo/EFO_0007904 GCST003991 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Photic sneeze reflex 32,446 European ancestry cases, 67,249 European ancestry controls NA Illumina [13729857] (imputed) 50 autosomal dominant compelling helio-ophthalmic outburst syndrome http://www.ebi.ac.uk/efo/EFO_0007887 GCST003992 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Menarche (age at onset) 76,831 European ancestry individuals NA Illumina [12039492] 44 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST003993 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Age at voice drop 55,871 European ancestry individuals NA Illumina [12039491] 14 age at voice drop http://www.ebi.ac.uk/efo/EFO_0007888 GCST003994 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Tonsillectomy 60,098 European ancestry cases, 113,323 European ancestry controls NA Illumina [13757430] (imputed) 36 tonsillectomy risk measurement http://www.ebi.ac.uk/efo/EFO_0007924 GCST003995 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Monobrow 69,284 European ancestry individuals NA Illumina [12039491] (imputed) 50 synophrys measurement http://www.ebi.ac.uk/efo/EFO_0007906 GCST003996 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Myopia 106,086 European ancestry cases, 85,757 European ancestry controls NA Illumina [13762925] (imputed) 51 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST003997 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Joint mobility (Beighton score) 64,143 European ancestry individuals NA Illumina [12039492] (imputed) 25 joint hypermobility measurement http://www.ebi.ac.uk/efo/EFO_0007905 GCST003998 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Nose size 67,023 European ancestry individuals NA Illumina [12039491] (imputed) 25 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST003999 Genome-wide genotyping array 2017-05-11 27182965 Pickrell JK 2016-05-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27182965 Detection and interpretation of shared genetic influences on 42 human traits. Male-pattern baldness 9,009 European ancestry cases, 8,491 European ancestry controls NA Illumina [13436641] (imputed) 44 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST003983 Genome-wide genotyping array 2017-06-05 28224759 Pei YF 2017-02-22 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/28224759 Genomic variants at 20p11 associated with body fat mass in the European population. Body fat mass 9,179 European ancestry individuals NA Affymetrix [6817908] (imputed) 3 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST004141 Genome-wide genotyping array 2017-04-04 27723756 Wang J 2016-10-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27723756 Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota. Gut microbiota (beta diversity) 1,812 European ancestry individuals 371 European ancestry individuals Affymetrix, Illumina [6344846] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST003876 Genome-wide genotyping array 2017-04-04 27723756 Wang J 2016-10-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27723756 Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota. Gut microbiota (bacterial taxa) 1,812 European ancestry individuals NA Affymetrix, Illumina [6344846] (imputed) 51 gut microbiome measurement, taxonomic microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874, http://www.ebi.ac.uk/efo/EFO_0007883 GCST003875 Genome-wide genotyping array 2017-06-02 28073927 Springelkamp H 2017-01-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28073927 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Optic cup area 20,353 European ancestry individuals, 2,131 Erasmus Rucphen (founder/genetic isolate) individuals 7,333 Asian ancestry individuals Affymetrix, Illumina [~ 8000000] (imputed) 47 optic cup area measurement http://www.ebi.ac.uk/efo/EFO_0006940 GCST004137 Genome-wide genotyping array 2017-05-24 28073927 Springelkamp H 2017-01-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28073927 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Vertical cup-disc ratio 21,768 European ancestry individuals, 2,131 Erasmus Rucphen (founder/genetic isolate) individuals 8,168 Asian ancestry individuals Affymetrix, Illumina [~ 8000000] (imputed) 46 cup-to-disc ratio measurement http://www.ebi.ac.uk/efo/EFO_0006939 GCST004075 Genome-wide genotyping array 2017-05-24 28073927 Springelkamp H 2017-01-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28073927 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Optic disc area 20,373 European ancestry individuals, 2,131 Erasmus Rucphen (founder/genetic isolate) individuals 7,302 Asian ancestry individuals Affymetrix, Illumina [~ 8000000] (imputed) 32 optic disc area measurement http://www.ebi.ac.uk/efo/EFO_0006937 GCST004076 Genome-wide genotyping array 2017-05-24 28073927 Springelkamp H 2017-01-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28073927 New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics. Intraocular pressure 25,916 European ancestry individuals, 1,073 Orcadian (founder/genetic isolate) individuals, 2,589 Erasmus Rucphen (founder/genetic isolate) individuals 8,352 Asian ancestry individuals Affymetrix, Illumina [~ 8000000] (imputed) 17 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST004074 Genome-wide genotyping array 2017-05-23 28203683 Heit JA 2017-02-16 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/28203683 Identification of unique venous thromboembolism-susceptibility variants in African-Americans. Venous thromboembolism adjusted for sickle cell variant rs77121243-T 393 African American cases, 4,941 African American controls. NR Affymetrix, Illumina [14074516] (imputed) 86 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST004068 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Diastolic blood pressure 19,546 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 4 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST004203 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Systolic blood pressure 19,547 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST004204 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Pulse pressure 19,546 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 0 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST004205 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Fasting plasma glucose 15,226 British ancestry non-diabetics individuals from 6863 families, 948 British ancestry diabetic individuals from 6863 families. NA Illumina [24111857] (imputed) 16 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST004206 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. HDL cholesterol 19,223 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 25 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST004207 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Body mass index 19,900 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 5 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004208 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Cholesterol, total 19,259 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 17 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST004209 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Body fat percentage 19,480 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 6 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST004210 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Urate levels 2077 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 4 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST004211 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Height 19,965 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 32 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST004212 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Resting heart rate 19,920 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 6 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST004213 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Creatinine levels 16,347 British ancestry from 6863 families. NA Illumina [24111857] (imputed) 4 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST004214 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Urea levels 19,293 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 5 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST004215 Genome-wide genotyping array 2017-06-21 28270201 Nagy R 2017-03-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/28270201 Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants. Waist-to-hip ratio adjusted for body mass index 19,695 British ancestry individuals from 6863 families. NA Illumina [24111857] (imputed) 4 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST004216 Genome-wide genotyping array 2017-07-01 28135244 Warren HR 2017-01-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28135244 Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Diastolic blood pressure 140,886 European ancestry individuals 190,318 European ancestry individuals Affymetrix [~ 9800000] (imputed) 94 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST004280 Genome-wide genotyping array 2017-07-01 28135244 Warren HR 2017-01-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28135244 Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Pulse pressure 140,886 European ancestry individuals 190,318 European ancestry individuals Affymetrix [~ 9800000] (imputed) 94 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST004278 Genome-wide genotyping array 2017-07-01 28135244 Warren HR 2017-01-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28135244 Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk. Systolic blood pressure 140,882 European ancestry individuals 190,318 European ancestry individuals Affymetrix [~ 9800000] (imputed) 42 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST004279 Genome-wide genotyping array 2017-06-26 28283553 Srinivasan L 2017-03-10 Arch Dis Child Fetal Neonatal Ed www.ncbi.nlm.nih.gov/pubmed/28283553 Genome-wide association study of sepsis in extremely premature infants. Sepsis in extremely premature infants 155 European ancestry cases, 190 non-European ancestry cases, 184 European ancestry controls, 222 non-European ancestry controls NA Illumina [7200000] (imputed) 6 Neonatal sepsis http://purl.obolibrary.org/obo/HP_0040187 GCST004230 Genome-wide genotyping array 2017-07-04 28317342 Hivert MF 2017-03-20 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/28317342 Genetic determinants of adiponectin regulation revealed by pregnancy. Adiponectin levels in pregnancy 1,322 European ancestry individuals 522 European ancestry individuals, 174 French Canadian founder individuals Illumina [NR] 3 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST004289 Genome-wide genotyping array 2017-06-12 28222112 Dumitrescu L 2017-01-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/28222112 Genome-wide study of resistant hypertension identified from electronic health records. Resistance to antihypertensive treatment in hypertension 1,719 European ancestry resistant cases, 708 European ancestry controlled hypertensives, 1,111 African American, Hispanic and other ancestry resistant cases, 168 African American, Hispanic and other ancestry controlled hypertensives NA Affymetrix, Illumina [2530150] (imputed) 6 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST004163 Genome-wide genotyping array 2017-05-25 28139693 Hoffmann TJ 2017-01-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28139693 Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer. Prostate-specific antigen levels 28,503 European ancestry individuals 2,716 Latino individuals, 2,518 East Asian ancestry individuals, 1,585 African American individuals, 6,193 European ancestry individuals (later diagnosed with prostate cancer), 5,603 European ancestry individuals Affymetrix [10109774] (imputed) 40 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST004093 Genome-wide genotyping array 2017-05-25 28139693 Hoffmann TJ 2017-01-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28139693 Genome-wide association study of prostate-specific antigen levels identifies novel loci independent of prostate cancer. Prostate-specific antigen levels (conditioned on lead SNPs) 28,503 European ancestry individuals 2,716 Latino individuals, 2,518 East Asian ancestry individuals, 1,585 African American individuals, 6,193 European ancestry individuals (later diagnosed with prostate cancer) Affymetrix [10109774] (imputed) 21 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST004094 Genome-wide genotyping array 2017-05-11 28029757 Merkel PA 2016-12-28 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28029757 Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis. Vasculitis associated with antineutrophil cytoplasmic antibody reactive to myeloperoxidase 324 European ancestry cases and 3258 European ancestry controls. 54 European ancestry cases and 1465 European ancestry controls. Affymetrix [at least 333035] (imputed) 1 anti-neutrophil antibody associated vasculitis http://www.ebi.ac.uk/efo/EFO_0004826 GCST003977 Genome-wide genotyping array 2017-05-11 28029757 Merkel PA 2016-12-28 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28029757 Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis. Vasculitis associated with antineutrophil cytoplasmic antibody reactive to proteinase-3 882 European ancestry cases and 3258 European ancestry controls. 479 European ancestry cases and 1465 European ancestry controls. Affymetrix [at least 333035] (imputed) 0 anti-neutrophil antibody associated vasculitis http://www.ebi.ac.uk/efo/EFO_0004826 GCST003978 Genome-wide genotyping array 2017-05-11 28029757 Merkel PA 2016-12-28 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28029757 Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody-Associated Vasculitis. Antineutrophil cytoplasmic antibody-associated vasculitis 1,015 European ancestry granulomatosis with polyangiitis cases, 206 European ancestry microscopic polyangiitis cases, 3,258 European ancestry controls. 541 European ancestry granulomatosis with polyangiitis cases, 30 European ancestry microscopic polyangiitis cases, 1,465 European ancestry controls. Affymetrix [at least 333035] (imputed) 6 anti-neutrophil antibody associated vasculitis http://www.ebi.ac.uk/efo/EFO_0004826 GCST003976 Genome-wide genotyping array 2017-03-31 27694959 Bonder MJ 2016-10-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27694959 The effect of host genetics on the gut microbiome. Gut microbiota (functional units) 984 European ancestry individuals 530 European ancestry individuals Illumina [8100000] (imputed) 56 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST003854 Genome-wide genotyping array 2017-03-31 27694959 Bonder MJ 2016-10-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27694959 The effect of host genetics on the gut microbiome. Gut microbiota (bacterial taxa) 984 European ancestry individuals 530 European ancestry individuals Illumina [8100000] (imputed) 21 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST003855 Genome-wide genotyping array 2019-02-10 27841878 Hoffmann TJ 2016-11-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27841878 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Diastolic blood pressure 295,529 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 2,029 African British individuals, 7,701 East Asian ancestry individuals, 2,735 South Asian ancestry individuals, 1,979 mixed and unknown ancestry individuals NA Affymetrix [at least 2696785] (imputed) 237 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST007094 Genome-wide genotyping array 2019-02-10 27841878 Hoffmann TJ 2016-11-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27841878 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Pulse pressure 295,529 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 2,029 African British individuals, 7,701 East Asian ancestry individuals, 2,735 South Asian ancestry individuals, 1,979 mixed and unknown ancestry individuals NA Affymetrix [at least 2696785] (imputed) 257 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST007096 Genome-wide genotyping array 2019-02-10 27841878 Hoffmann TJ 2016-11-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27841878 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Systolic blood pressure 295,529 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 2,029 African British individuals, 7,701 East Asian ancestry individuals, 2,735 South Asian ancestry individuals, 1,979 mixed and unknown ancestry individuals NA Affymetrix [at least 2696785] (imputed) 260 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST007099 Genome-wide genotyping array 2019-02-10 27841878 Hoffmann TJ 2016-11-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27841878 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Diastolic blood pressure 80,792 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 7,243 East Asian ancestry individuals, 461 South Asian ancestry individuals NA Affymetrix [at least 2696785] (imputed) 127 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST007098 Genome-wide genotyping array 2019-02-10 27841878 Hoffmann TJ 2016-11-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27841878 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Pulse pressure 80,792 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 7,243 East Asian ancestry individuals, 461 South Asian ancestry individuals NA Affymetrix [at least 2696785] (imputed) 169 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST007097 Genome-wide genotyping array 2019-02-10 27841878 Hoffmann TJ 2016-11-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27841878 Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. Systolic blood pressure 80,792 European ancestry individuals, 8,231 Latino individuals, 3,058 African American individuals, 7,243 East Asian ancestry individuals, 461 South Asian ancestry individuals NA Affymetrix [at least 2696785] (imputed) 144 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST007095 Genome-wide genotyping array 2017-03-31 27659466 van der Harst P 2016-09-27 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/27659466 52 Genetic Loci Influencing Myocardial Mass. QRS duration 59,565 European ancestry individuals, 690 Orcadian (founder/genetic isolate) individuals 13,263 European ancestry individuals, 3,603 African American individuals, 4,619 Indian ancestry individuals Affymetrix, Illumina, Perlegen [at least 2766983] (imputed) 47 QRS complex, QRS duration http://www.ebi.ac.uk/efo/EFO_0005054, http://www.ebi.ac.uk/efo/EFO_0005055 GCST003844 Genome-wide genotyping array 2017-04-01 27659466 van der Harst P 2016-09-27 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/27659466 52 Genetic Loci Influencing Myocardial Mass. QRS complex (12-leadsum) up to 47,942 European ancestry individuals, up to 690 Orcadian (founder/genetic isolate) individuals 13,263 European ancestry individuals, 3,603 African American individuals, 4,619 Indian ancestry individuals Affymetrix, Illumina, Perlegen [2766983] (imputed) 21 QRS amplitude, QRS complex http://www.ebi.ac.uk/efo/EFO_0007742, http://www.ebi.ac.uk/efo/EFO_0005054 GCST003872 Genome-wide genotyping array 2017-04-01 27659466 van der Harst P 2016-09-27 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/27659466 52 Genetic Loci Influencing Myocardial Mass. QRS complex (Cornell) up to 58,172 European ancestry individuals, up to 690 Orcadian (founder/genetic isolate) individuals 13,263 European ancestry individuals, 3,603 African American individuals, 4,619 Indian ancestry individuals Affymetrix, Illumina, Perlegen [2766983] (imputed) 17 QRS amplitude, QRS complex http://www.ebi.ac.uk/efo/EFO_0007742, http://www.ebi.ac.uk/efo/EFO_0005054 GCST003871 Genome-wide genotyping array 2017-04-01 27659466 van der Harst P 2016-09-27 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/27659466 52 Genetic Loci Influencing Myocardial Mass. QRS complex (Sokolow-Lyon) up to 54,303 European ancestry individuals, up to 690 Orcadian (founder/genetic isolate) individuals 13,263 European ancestry individuals, 3,603 African American individuals, 4,619 Indian ancestry individuals Affymetrix, Illumina, Perlegen [2766983] (imputed) 9 QRS amplitude, QRS complex http://www.ebi.ac.uk/efo/EFO_0007742, http://www.ebi.ac.uk/efo/EFO_0005054 GCST003870 Genome-wide genotyping array 2017-06-29 28388302 Petros Z 2017-04-01 OMICS www.ncbi.nlm.nih.gov/pubmed/28388302 Genome-Wide Association and Replication Study of Hepatotoxicity Induced by Antiretrovirals Alone or with Concomitant Anti-Tuberculosis Drugs. Liver injury in anti-retroviral drug treated HIV 14 Ethiopian cases with HIV, 293 Ethiopian controls with HIV. 7 Ethiopian cases with HIV, 66 Ethiopian controls with HIV. Illumina [662282] 1 response to efavirenz, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0006904, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004261 Genome-wide genotyping array 2017-06-29 28388302 Petros Z 2017-04-01 OMICS www.ncbi.nlm.nih.gov/pubmed/28388302 Genome-Wide Association and Replication Study of Hepatotoxicity Induced by Antiretrovirals Alone or with Concomitant Anti-Tuberculosis Drugs. Liver injury in combined anti-retroviral and anti-tuberculosis drug-treated HIV with tuberculosis 27 Ethiopian cases with HIV and tuberculosis, 159 Ethiopian controls with HIV and tuberculosis. 8 Ethiopian cases with HIV and tuberculosis, up to 108 Ethiopian controls with HIV and tuberculosis. Illumina [662807] 3 response to rifampicin, response to efavirenz, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007866, http://www.ebi.ac.uk/efo/EFO_0006904, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004262 Genome-wide genotyping array 2017-03-17 27643478 Powers A 2016-09-09 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/27643478 A genome-wide association study of emotion dysregulation: Evidence for interleukin 2 receptor alpha. Emotional dysregulation 774 African American males, 1,826 African American females NA Illumina [883511] 1 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST003765 Genome-wide genotyping array 2017-06-08 28166215 Hobbs BD 2017-02-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28166215 Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. Chronic obstructive pulmonary disease 11,157 European ancestry cases, 36,699 European ancestry controls, 1,142 African American cases, 2,380 African American controls, 199 Korean ancestry cases, 6,741 Korean ancestry controls, 52 Hispanic cases, 548 Hispanic controls. 12,051 European ancestry cases, 11,111 European ancestry controls, 153 Korean ancestry cases, 205 Korean ancestry controls. Affymetrix, Illumina [NR] (imputed) 31 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST004147 Genome-wide genotyping array 2017-06-15 28118524 Saxena R 2017-01-24 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28118524 A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis. Rheumatoid arthritis 97 African admixed Arab ancestry cases, 410 non-African admixed Arab ancestry cases, 4 Arab ancestry cases, 56 African admixed Arab ancestry controls, 290 non-African admixed Arab ancestry controls, 6 Arab ancestry controls 283 Arab ancestry cases, 221 Arab ancestry controls Illumina [7000653] (imputed) 4 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST004172 Genome-wide genotyping array 2017-06-15 28118524 Saxena R 2017-01-24 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28118524 A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis. Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive) 357 African admixed and non-African admixed Arab ancestry cases, 352 African admixed and non-African admixed Arab ancestry controls 234 Arab ancestry cases, 225 Arab ancestry controls Illumina [7000653] (imputed) 4 rheumatoid arthritis, anti-citrullinated protein antibody seropositivity, rheumatoid factor seropositivity measurement http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0007837, http://www.ebi.ac.uk/efo/EFO_0007791 GCST004174 Genome-wide genotyping array 2017-06-15 28118524 Saxena R 2017-01-24 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/28118524 A Multinational Arab Genome-Wide Association Study Identifies New Genetic Associations for Rheumatoid Arthritis. Rheumatoid arthritis (rheumatoid factor and anti-cyclic citrullinated peptide seronegative) 154 African admixed and non-African admixed Arab ancestry cases, 352 African admixed and non-African admixed Arab ancestry controls 54 Arab ancestry cases, 225 Arab ancestry controls Illumina [7000653] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST004173 Genome-wide genotyping array 2017-05-26 28120872 Li X 2017-01-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28120872 Genome-wide association study identifies four SNPs associated with response to platinum-based neoadjuvant chemotherapy for cervical cancer. Response to platinum-based neoadjuvant chemotherapy in cervical cancer 66 Han Chinese ancestry non-responder cases, 160 Han Chinese ancestry responder cases 79 Han Chinese ancestry non-responder cases, 291 Han Chinese ancestry responder cases Affymetrix [657178] 3 response to platinum-based neoadjuvant chemotherapy http://www.ebi.ac.uk/efo/EFO_0007943 GCST004097 Genome-wide genotyping array 2017-06-08 28165464 Law PJ 2017-02-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28165464 Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. Chronic lymphocytic leukemia 4,478 European ancestry cases and 13,213 European ancestry controls. 1,722 European ancestry cases and 4,385 European ancestry controls. Affymetrix, Illumina [> 10000000] (imputed) 37 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST004146 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Carotenoid levels (cryptoxanthin) 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 0 cryptoxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007897 GCST003934 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Carotenoid levels (alpha-carotene) 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 3 alpha-carotene measurement http://www.ebi.ac.uk/efo/EFO_0007893 GCST003938 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Vitamin E levels (alpha-tocopherol) 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST003935 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Carotenoid levels (beta-carotene) 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 0 beta-carotene measurement http://www.ebi.ac.uk/efo/EFO_0007894 GCST003931 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Carotenoid levels (lutein) 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 0 lutein measurement http://www.ebi.ac.uk/efo/EFO_0007895 GCST003932 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Carotenoid levels (zeaxanthin) 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 0 zeaxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007896 GCST003933 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Vitamin E levels (gamma-tocopherol) 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 0 gamma-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007899 GCST003936 Genome-wide genotyping array 2017-04-21 28002826 D'Adamo CR 2016-12-22 J Nutrigenet Nutrigenomics www.ncbi.nlm.nih.gov/pubmed/28002826 The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations. Retinol levels 433 Old Order Amish individuals NA Affymetrix [2193082] (imputed) 0 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST003937 Genome-wide genotyping array 2017-03-16 27669027 Boueiz A 2016-09-26 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/27669027 Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution. Emphysema distribution in smoking 7,039 European ancestry individuals, 2,955 African American individuals, 1538 individuals NA Illumina [at least 10657975] (imputed) 9 emphysema pattern measurement http://www.ebi.ac.uk/efo/EFO_0005850 GCST003761 Genome-wide genotyping array 2020-01-09 28132517 Xie W 2017-01-28 AIDS Res Hum Retroviruses www.ncbi.nlm.nih.gov/pubmed/28132517 Genome-Wide Analyses Reveal Gene Influence on HIV Disease Progression and HIV-1C Acquisition in Southern Africa. HIV progression (CD4 and viral load) 556 Motswana ancestry cases NA Illumina [NR] 7 viral load, disease progression measurement, CD4-positive T-lymphocyte count, HIV infection http://www.ebi.ac.uk/efo/EFO_0010125, http://www.ebi.ac.uk/efo/EFO_0008336, http://www.ebi.ac.uk/efo/EFO_0010105, http://www.ebi.ac.uk/efo/EFO_0000764 GCST009417 Genome-wide genotyping array 2017-06-06 28212542 Ransohoff KJ 2017-02-09 Oncotarget www.ncbi.nlm.nih.gov/pubmed/28212542 Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma. Melanoma 4,842 European ancestry cases, 286,565 European ancestry controls 1,804 European ancestry cases, 1,026 European ancestry controls Illumina [at least 560000] (imputed) 28 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST004142 Genome-wide genotyping array 2017-06-06 28195142 Gudmundsson J 2017-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28195142 A genome-wide association study yields five novel thyroid cancer risk loci. Thyroid cancer 2,637 European ancestry cases, 364 non-array typed, familial imputed Icelandic ancestry cases, 134,811 European ancestry controls, 152,739 non-array typed, familial imputed Icelandic ancestry controls. NA Illumina [7100000] (imputed) 12 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST004144 Genome-wide genotyping array 2017-06-13 28130311 Tan W 2017-01-27 Gut www.ncbi.nlm.nih.gov/pubmed/28130311 Genome-wide association study identifies HLA-DR variants conferring risk of HBV-related acute-on-chronic liver failure. Acute-on-chronic liver failure in hepatitis B 389 Chinese ancestry cases, 391 Chinese ancestry controls 901 Chinese ancestry cases, 1,686 Chinese ancestry controls Affymetrix [654960] 1 acute-on-chronic liver failure http://www.ebi.ac.uk/efo/EFO_0007949 GCST004165 Genome-wide genotyping array 2017-06-04 28139761 Pasanen A 2017-01-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28139761 Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis. Bronchiolitis 217 European ancestry child cases, 778 European ancestry controls 618 European ancestry child cases, 1,318 European ancestry controls Illumina [5304323] (imputed) 0 Bronchiolitis http://purl.obolibrary.org/obo/HP_0011950 GCST004140 Genome-wide genotyping array 2017-05-11 28098162 Hibar DP 2017-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28098162 Novel genetic loci associated with hippocampal volume. Hippocampal volume 26,814 European ancestry individuals up to 3,863 European ancestry individuals, up to 562 African American individuals, up to 886 Asian ancestry individuals, up to 1,411 Mexican American individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 2 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST003961 Genome-wide genotyping array 2017-05-24 28087736 Ludwig KU 2017-01-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28087736 Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only. Nonsyndromic cleft lip with or without cleft palate 399 European ancestry cases, 1,318 European ancestry controls, 666 European ancestry trios, 795 Asian trios 224 European ancestry cases, 921 European ancestry controls, 152 Mayan cases, 323 Mayan controls, 198 Middle Eastern cases, 391 Middle Eastern controls NR [8012124] (imputed) 13 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST004088 Genome-wide genotyping array 2017-05-24 28087736 Ludwig KU 2017-01-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28087736 Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only. Cleft palate 550 European, Asian and unknown trios NA NR [~ 8380000] (imputed) 0 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST004089 Genome-wide genotyping array 2017-06-26 28179588 Fagerholm R 2017-03-14 Oncotarget www.ncbi.nlm.nih.gov/pubmed/28179588 TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer. Survival in breast cancer (TP53 expression interaction) 572 Finnish ancestry cases 4,610 European ancestry cases NR [NR] 0 overall survival, breast carcinoma, TP53 mutation status http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0008382 GCST004229 Genome-wide genotyping array 2017-06-26 28179588 Fagerholm R 2017-03-14 Oncotarget www.ncbi.nlm.nih.gov/pubmed/28179588 TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer. Survival in TP53 positive breast cancer 157 Finnish ancestry cases NR [NR] 0 overall survival, TP53 Positive Breast Carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1002010 GCST004228 Genome-wide genotyping array 2018-08-16 28082259 Pankow JS 2017-01-12 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/28082259 Identification of Genetic Variants Linking Protein C and Lipoprotein Metabolism: The ARIC Study (Atherosclerosis Risk in Communities). Protein C levels 10,778 European ancestry individuals, 2,706 African American individuals NA Affymetrix [at least 22484459] (imputed) 11 protein C measurement http://www.ebi.ac.uk/efo/EFO_0004633 GCST006119 Genome-wide genotyping array 2017-06-02 28115739 Smith AH 2017-01-24 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28115739 Genome-wide association study of therapeutic opioid dosing identifies a novel locus upstream of OPRM1. Methadone dose in opioid dependence 1,027 European American cases, 383 African American cases NA Illumina [at least 988306] (imputed) 37 methadone dose measurement http://www.ebi.ac.uk/efo/EFO_0007907 GCST004136 Genome-wide genotyping array 2017-05-12 28039329 Noordam R 2016-12-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/28039329 A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. QT interval (tricyclic/tetracyclic antidepressant use interaction) 1,250 European ancestry users, 295 African American users, 1,886 Hispanic or Latino ancestry users, 40,701 European ancestry non-users, 9,940 African American non-users, 67,863 Hispanic or Latino ancestry non-users NA Affymetrix, Illumina [NR] (imputed) 1 response to tetracyclic antidepressant, QT interval, response to tricyclic antidepressant http://www.ebi.ac.uk/efo/EFO_0007917, http://www.ebi.ac.uk/efo/EFO_0004682, http://www.ebi.ac.uk/efo/EFO_0007916 GCST004010 Genome-wide genotyping array 2017-05-12 28039329 Noordam R 2016-12-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/28039329 A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. RR interval (tricyclic/tetracyclic antidepressant use interaction) 1,417 European ancestry users, 295 African American users, 174 Hispanic or Latino ancestry users, 44,289 European ancestry non-users, 9,940 African American non-users, 13,634 Hispanic or Latino ancestry non-users NA Affymetrix, Illumina [NR] (imputed) 3 RR interval, response to tetracyclic antidepressant, response to tricyclic antidepressant http://www.ebi.ac.uk/efo/EFO_0004831, http://www.ebi.ac.uk/efo/EFO_0007917, http://www.ebi.ac.uk/efo/EFO_0007916 GCST004011 Genome-wide genotyping array 2017-06-30 28289848 Haralambieva IH 2017-04-01 Hum Genet www.ncbi.nlm.nih.gov/pubmed/28289848 Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine. Immune response to measles vaccine (measles-specific neutralising antibody titre) 2,555 European ancestry individuals, 317 African American individuals NA Illumina [at least 508199] 6 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST004269 Genome-wide genotyping array 2017-06-30 28289848 Haralambieva IH 2017-04-01 Hum Genet www.ncbi.nlm.nih.gov/pubmed/28289848 Genome-wide associations of CD46 and IFI44L genetic variants with neutralizing antibody response to measles vaccine. Immune response to measles vaccine (measles-induced IFN gamma) up to 2,555 European ancestry individuals, up to 317 African American individuals NA Illumina [at least 508199] 1 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST004268 Genome-wide genotyping array 2017-06-28 28296344 Chen G 2017-03-13 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/28296344 Genome-wide analysis identifies an african-specific variant in SEMA4D associated with body mass index. Body mass index 1,570 West African individuals 1,411 West African individuals, 9,020 African American individuals Affymetrix [13412051] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004255 Genome-wide genotyping array 2017-05-31 28073367 Zeng X 2017-01-10 Respir Res www.ncbi.nlm.nih.gov/pubmed/28073367 No convincing association between genetic markers and respiratory symptoms: results of a GWA study. Phlegm 7,976 Dutch ancestry individuals 6,789 Dutch ancestry individuals Illumina [at least 227981] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST004111 Genome-wide genotyping array 2017-05-31 28073367 Zeng X 2017-01-10 Respir Res www.ncbi.nlm.nih.gov/pubmed/28073367 No convincing association between genetic markers and respiratory symptoms: results of a GWA study. Dyspnea 7,976 Dutch ancestry individuals 6,789 Dutch ancestry individuals Illumina [at least 227981] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST004112 Genome-wide genotyping array 2017-05-23 28073367 Zeng X 2017-01-10 Respir Res www.ncbi.nlm.nih.gov/pubmed/28073367 No convincing association between genetic markers and respiratory symptoms: results of a GWA study. Cough 7,976 Dutch ancestry individuals 6,789 Dutch ancestry individuals Illumina [at least 227981] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST004073 Genome-wide genotyping array 2017-07-10 28416818 Christophersen IE 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416818 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Atrial fibrillation 15,979 European ancestry cases, 102,776 European ancestry controls, 641 African American cases, 5,234 African American controls, 837 Japanese ancestry cases, 3,293 Japanese controls, 277 Hispanic cases, 3,081 Hispanic controls,197 Brazilian ancestry cases, 758 Brazilian ancestry controls. 8,180 Japanese ancestry cases, 28,612 Japanese ancestry controls. Affymetrix, Illumina [11795432] (imputed) 10 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004295 Genome-wide genotyping array 2017-07-10 28416818 Christophersen IE 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416818 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Atrial fibrillation 15,979 European ancestry cases, 102,776 European ancestry controls, 641 African American cases, 5,234 African American controls, 837 Japanese ancestry cases, 3,293 Japanese controls, 277 Hispanic cases, 3,081 Hispanic controls,197 Brazilian ancestry cases, 758 Brazilian ancestry controls. 3,666 cases, 139,852 controls Affymetrix, Illumina [11795432] (imputed) 8 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004296 Genome-wide genotyping array 2017-07-10 28416818 Christophersen IE 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416818 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Atrial fibrillation 15,979 European ancestry cases, 102,776 European ancestry controls. NA Affymetrix, Illumina [11795432] (imputed) 20 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004297 Genome-wide genotyping array 2017-07-10 28416818 Christophersen IE 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416818 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Atrial fibrillation 837 Japanese ancestry cases, 3,293 Japanese controls 8,180 Japanese ancestry cases, 28,612 Japanese ancestry controls. Affymetrix, Illumina [11795432] (imputed) 1 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004298 Genome-wide genotyping array 2017-07-10 28416818 Christophersen IE 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416818 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Atrial fibrillation 641 African American cases, 5,234 African American controls 447 African American cases, 442 African American controls Affymetrix, Illumina [11795432] (imputed) 1 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004299 Genome-wide genotyping array 2017-07-10 28416818 Christophersen IE 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416818 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Incident atrial fibrillation 7,323 European ancestry cases, 102,776 European ancestry controls. Affymetrix, Illumina [at least 3187278] (imputed) 5 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004300 Genome-wide genotyping array 2017-07-10 28416818 Christophersen IE 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416818 Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Prevalent atrial fibrillation 8,656 European ancestry cases, 102,776 European ancestry controls. Affymetrix, Illumina [at least 3187278] (imputed) 9 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004301 Genome-wide genotyping array 2017-06-29 28358823 Kim SK 2017-03-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/28358823 Genome-wide association screens for Achilles tendon and ACL tears and tendinopathy. Achilles tendinopathy 4,258 European ancestry cases, 413 Latin-American cases, 268 East Asian ancestry cases, 192 African American cases, 17 South East Asian ancestry cases, 79,006 European ancestry controls, 8,147 Latin-American controls, 7,250 East Asian ancestry controls, 2,969 African American controls, 459 South East Asian ancestry controls Affymetrix [10551193] (imputed) 4 Tendinopathy http://www.ebi.ac.uk/efo/EFO_1001434 GCST004263 Genome-wide genotyping array 2017-06-29 28358823 Kim SK 2017-03-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/28358823 Genome-wide association screens for Achilles tendon and ACL tears and tendinopathy. Anterior cruciate ligament rupture 495 European ancestry cases, 54 Latin-American cases, 49 East Asian ancestry cases, 82,769 European ancestry controls, 8,506 Latin-American controls, 7,469 East Asian ancestry controls Affymetrix [8303052] (imputed) 3 ligament rupture http://www.ebi.ac.uk/efo/EFO_1002012 GCST004265 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Peak velocity of the mitral E-wave 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004653 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Isovolumetric relaxation time 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 5 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004649 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Peak velocity of excursion of lateral mitral annulus in early diastolic phase 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004658 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Peak velocity of the mitral A-wave 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 2 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004652 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Ratio of the peak velocity of the mitral E-Wave divided by the peak velocity of the mitral A-wave. 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 1 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004656 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Deceleration time of the mitral E-wave 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004654 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Ratio of the peak velocity of the excursion of the lateral mitral annulus in the early diastolic phase and the peak velocity of the mitral E-wave 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004657 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Diastolic dysfunction with preserved ejection pressure 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004650 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Heart failure with preserved ejection fraction 21,852 European ancestry individuals 14,787 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST004660 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Aortic root size 30,201 European ancestry individuals 14,002 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 8 aortic root size http://www.ebi.ac.uk/efo/EFO_0005037 GCST004651 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Left atrial antero-posterior diameter 30,201 European ancestry individuals NA Affymetrix, Illumina [at least 283291] (imputed) 16 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST004647 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Left ventricle diastolic internal dimension 30,201 European ancestry individuals 14,002 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 2 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST004655 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Left ventricle wall thickness 30,201 European ancestry individuals NA Affymetrix, Illumina [at least 283291] (imputed) 21 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST004646 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Left ventricular mass 30,201 European ancestry individuals 14,002 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 1 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST004659 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Left ventricular fractional shortening 30,201 European ancestry individuals 14,002 European ancestry individuals Affymetrix, Illumina [at least 283291] (imputed) 1 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST004645 Genome-wide genotyping array 2017-09-05 28394258 Wild PS 2017-04-10 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/28394258 Large-scale genome-wide analysis identifies genetic variants associated with cardiac structure and function. Left ventricle systolic dysfunction 30,201 European ancestry individuals NA Affymetrix, Illumina [at least 283291] (imputed) 6 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST004648 Genome-wide genotyping array 2017-03-27 27798624 Eppinga RN 2016-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27798624 Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality. Resting heart rate 127,919 European ancestry individuals, 2,478 Asian ancestry individuals, 1,734 Black individuals, 684 Mixed ancestry individuals, 1,436 individuals 130,795 European ancestry individuals Affymetrix [19941912] (imputed) 86 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST003818 Genome-wide genotyping array 2017-03-31 28171582 Gao X 2016-11-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28171582 Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos. Central corneal thickness 3,584 Latino individuals 931 Latino individuals Illumina [576798] (imputed) 6 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST003856 Genome-wide genotyping array 2017-03-31 27647854 Sandholm N 2016-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27647854 The Genetic Landscape of Renal Complications in Type 1 Diabetes. Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes 729 European ancestry cases, 84 cases, 3,290 European ancestry controls, 705 controls 94 European ancestry cases, 964 cases, 993 European ancestry controls, 4806 controls Illumina [NR] (imputed) 2 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST003862 Genome-wide genotyping array 2017-03-31 27647854 Sandholm N 2016-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27647854 The Genetic Landscape of Renal Complications in Type 1 Diabetes. Kidney disease (end stage renal disease vs normoalbuminuria) in type 1 diabetes 729 European ancestry cases, 84 cases, 1,903 European ancestry controls, 491 controls 94 European ancestry cases, 964 cases, 627 European ancestry controls, 3187 controls Illumina [NR] (imputed) 1 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST003861 Genome-wide genotyping array 2017-03-31 27647854 Sandholm N 2016-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27647854 The Genetic Landscape of Renal Complications in Type 1 Diabetes. Chronic kidney disease (severe chronic kidney disease vs normal kidney function) in type 1 diabetes 907 European ancestry cases, 210 cases, 1,661 European ancestry controls, 357 controls 1,266 cases, 2,655 controls Illumina [NR] (imputed) 2 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST003863 Genome-wide genotyping array 2017-03-31 27647854 Sandholm N 2016-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27647854 The Genetic Landscape of Renal Complications in Type 1 Diabetes. Kidney disease (early and late stages) in type 1 diabetes 2,068 European ancestry cases, 495 cases, 1,903 European ancestry controls, 690 controls 68 European ancestry cases, 3,188 cases, 815 European ancestry controls, 3,907 controls Illumina [NR] (imputed) 1 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST003864 Genome-wide genotyping array 2017-03-31 27647854 Sandholm N 2016-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27647854 The Genetic Landscape of Renal Complications in Type 1 Diabetes. Kidney disease (early stage) in type 1 diabetes 555 European ancestry cases, 245 cases, 1,903 European ancestry controls, 690 controls 602 cases, 1,459 controls Illumina [NR] (imputed) 3 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST003865 Genome-wide genotyping array 2017-03-31 27647854 Sandholm N 2016-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27647854 The Genetic Landscape of Renal Complications in Type 1 Diabetes. Kidney disease (late stage) in type 1 diabetes 1,507 European ancestry cases, 250 controls, 1,903 European ancestry controls, 690 controls 2,536 cases, 3,907 controls Illumina [NR] (imputed) 1 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST003866 Genome-wide genotyping array 2017-03-31 27647854 Sandholm N 2016-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27647854 The Genetic Landscape of Renal Complications in Type 1 Diabetes. Chronic kidney disease (chronic kidney disease vs normal or mildly reduced eGFR) in type 1 diabetes 1,142 European ancestry cases, 113 cases, 2,442 European ancestry controls, 467 controls 2,046 cases, 4,549 controls Illumina [NR] (imputed) 1 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST003867 Genome-wide genotyping array 2017-03-20 27650483 Kramer HJ 2016-09-20 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/27650483 African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos. Urinary albumin-to-creatinine ratio 5,458 Caribbean Hispanic/Latino individuals, 6,734 Mainland Hispanic/Latino individuals, 34 Hispanic/Latino individuals NA Illumina [2536661] (imputed) 3 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST003774 Genome-wide genotyping array 2017-04-24 27846281 Galesloot TE 2016-11-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/27846281 Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin. Hepcidin/transferrin saturation ratio 1495 European ancestry individuals without iron deficiency or clinical inflammation, 324 European ancestry individuals, 1206 Val Borbera (founder/genetic isolated) individuals without iron deficiency or clinical inflammation, 274 Val Borbera (founder/genetic isolated) individuals, 2,695 European ancestry individuals without iron deficiency or clinical inflammation, 207 individuals NA Illumina [up to 38043574] (imputed) 13 hepcidin:transferrin saturation ratio http://www.ebi.ac.uk/efo/EFO_0007902 GCST003945 Genome-wide genotyping array 2017-04-24 27846281 Galesloot TE 2016-11-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/27846281 Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin. Hepcidin/ferritin ratio 1495 European ancestry individuals without iron deficiency or clinical inflammation, 324 European ancestry individuals, 1206 Val Borbera (founder/genetic isolated) individuals without iron deficiency or clinical inflammation, 274 Val Borbera (founder/genetic isolated) individuals, 2,695 European ancestry individuals without iron deficiency or clinical inflammation, 207 individuals NA Illumina [up to 38043574] (imputed) 43 hepcidin:ferritin ratio http://www.ebi.ac.uk/efo/EFO_0007901 GCST003944 Genome-wide genotyping array 2017-04-24 27846281 Galesloot TE 2016-11-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/27846281 Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin. Hepcidin levels 1495 European ancestry individuals without iron deficiency or clinical inflammation, 324 European ancestry individuals, 1206 Val Borbera (founder/genetic isolated) individuals without iron deficiency or clinical inflammation, 274 Val Borbera (founder/genetic isolated) individuals, 2,695 European ancestry individuals without iron deficiency or clinical inflammation, 207 individuals 1,018 European ancestry individuals, 2,876 individuals Illumina [up to 38043574] (imputed) 7 serum hepcidin measurement http://www.ebi.ac.uk/efo/EFO_0004504 GCST003943 Genome-wide genotyping array 2017-06-12 28163062 Matsuura K 2017-02-02 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28163062 Genome-Wide Association Study Identifies TLL1 Variant Associated With Development of Hepatocellular Carcinoma After Eradication of Hepatitis C Virus Infection. Hepatocellular carcinoma in post hepatitis C eradication by interferon therapy 123 Japanese ancestry hepatocellular carcinoma cases, 333 Japanese ancestry 5-yr hepatocellular carcinoma-free controls 130 Japanese ancestry hepatocellular carcinoma cases, 210 Japanese ancestry 5-yr hepatocellular carcinoma-free controls Affymetrix [443299] 1 response to interferon, hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0007859, http://www.ebi.ac.uk/efo/EFO_0000182 GCST004160 Genome-wide genotyping array 2017-03-16 27664181 Kawamura R 2016-09-23 Physiol Genomics www.ncbi.nlm.nih.gov/pubmed/27664181 Genome-wide association study of plasma resistin levels identified rs1423096 and rs10401670 as possible functional variants in the Japanese population. Resistin levels 448 Japanese ancestry individuals 4,059 Japanese ancestry individuals Illumina [5708071] (imputed) 2 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST003759 Genome-wide genotyping array 2017-03-21 27656708 Zhang W 2016-09-22 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/27656708 Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels. L-arginine levels 901 European ancestry individuals, 1,394 Indian Asian ancestry individuals 1,000 European ancestry individuals, 2,981 individuals Illumina [~ 8000000] (imputed) 2 L-arginine measurement http://www.ebi.ac.uk/efo/EFO_0006524 GCST003793 Genome-wide genotyping array 2017-06-04 28115744 Ikeda M 2017-01-24 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28115744 A genome-wide association study identifies two novel susceptibility loci and trans population polygenicity associated with bipolar disorder. Bipolar disorder 2,964 Japanese ancestry case, 61,887 Japanese ancestry controls, 7,481 European ancestry cases, 9,250 European ancestry controls NA Illumina [at least 6195093] (imputed) 23 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST004139 Genome-wide genotyping array 2017-05-30 28112199 Law PJ 2017-01-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28112199 Genome-wide association analysis of chronic lymphocytic leukaemia, Hodgkin lymphoma and multiple myeloma identifies pleiotropic risk loci. B-cell malignancies (chronic lymphocytic leukemia, Hodgkin lymphoma or multiple myeloma) (pleiotropy) 1,842 European ancestry chronic lymphocytic leukemia cases, 1,465 European ancestry Hodgkin lymphoma cases, 3,790 European ancestry multiple myeloma cases, 7,324 European ancestry controls NA Illumina [10806625] (imputed) 20 Hodgkins lymphoma, multiple myeloma, chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000183, http://www.ebi.ac.uk/efo/EFO_0001378, http://www.ebi.ac.uk/efo/EFO_0000095 GCST004099 Genome-wide genotyping array 2017-05-30 28167838 Deckert J 2017-02-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28167838 GLRB allelic variation associated with agoraphobic cognitions, increased startle response and fear network activation: a potential neurogenetic pathway to panic disorder. Agoraphobic traits 1,370 German ancestry individuals 6,392 European ancestry individuals Illumina [7071105] (imputed) 0 agoraphobia symptom measurement http://www.ebi.ac.uk/efo/EFO_0007945 GCST004109 Genome-wide genotyping array 2017-05-25 28100725 Chen J 2017-01-18 Neurology www.ncbi.nlm.nih.gov/pubmed/28100725 Genome-wide association study identifies MAPT locus influencing human plasma tau levels. Plasma t-tau levels 463 European ancestry Alzheimer's disease cases, 163 European ancestry individuals with mild cognitive impairment, 151 European ancestry individuals 360 individuals, 27 individuals later diagnosed with mild cognitive impairment Illumina [316802] 4 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST004092 Genome-wide genotyping array 2017-05-24 28093568 Trampush JW 2017-01-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28093568 GWAS meta-analysis reveals novel loci and genetic correlates for general cognitive function: a report from the COGENT consortium. Cognitive function up to 35,298 European ancestry individuals NA Affymetrix, Illumina [8037763] (imputed) 13 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST004077 Genome-wide genotyping array 2017-05-15 27846195 Li Q 2016-11-11 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27846195 Genome-wide association study of paliperidone efficacy. Response to paliperidone in schizophrenia (positive Marder score) 1,390 European ancestry cases NA Illumina [~ 9000000] (imputed) 63 response to paliperidone, schizophrenia symptom severity measurement http://www.ebi.ac.uk/efo/EFO_0007925, http://www.ebi.ac.uk/efo/EFO_0007927 GCST004040 Genome-wide genotyping array 2017-05-15 27846195 Li Q 2016-11-11 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27846195 Genome-wide association study of paliperidone efficacy. Response to paliperidone in schizophrenia (negative Marder score) 1,390 European ancestry cases NA Illumina [~ 9000000] (imputed) 66 response to paliperidone, schizophrenia symptom severity measurement http://www.ebi.ac.uk/efo/EFO_0007925, http://www.ebi.ac.uk/efo/EFO_0007927 GCST004041 Genome-wide genotyping array 2017-05-15 27846195 Li Q 2016-11-11 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27846195 Genome-wide association study of paliperidone efficacy. Response to paliperidone in schizophrenia (PANSS score) 1,390 European ancestry individuals NA Illumina [~ 9000000] (imputed) 64 response to paliperidone, schizophrenia symptom severity measurement http://www.ebi.ac.uk/efo/EFO_0007925, http://www.ebi.ac.uk/efo/EFO_0007927 GCST004042 Genome-wide genotyping array 2017-05-15 27846195 Li Q 2016-11-11 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27846195 Genome-wide association study of paliperidone efficacy. Response to paliperidone in schizophrenia (Multivariate) 1,390 European ancestry individuals NA Illumina [~ 9000000] (imputed) 26 response to paliperidone, schizophrenia symptom severity measurement http://www.ebi.ac.uk/efo/EFO_0007925, http://www.ebi.ac.uk/efo/EFO_0007927 GCST004043 Genome-wide genotyping array 2017-05-15 27846195 Li Q 2016-11-11 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/27846195 Genome-wide association study of paliperidone efficacy. Response to paliperidone in schizophrenia (CGI-S score) 1,390 European ancestry cases NA Illumina [~ 9000000] (imputed) 30 response to paliperidone, schizophrenia symptom severity measurement http://www.ebi.ac.uk/efo/EFO_0007925, http://www.ebi.ac.uk/efo/EFO_0007927 GCST004039 Genome-wide genotyping array 2017-06-21 28314753 Terao C 2017-03-17 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/28314753 Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis. Systemic sclerosis 700 Japanese ancestry cases, 1,797 Japanese ancestry controls, 564 European ancestry cases, 1,776 European ancestry controls 564 Japanese ancestry cases, 1,863 Japanese ancestry controls, 2,592 European ancestry cases, 9,315 European ancestry controls Illumina [3610917] (imputed) 7 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST004202 Genome-wide genotyping array 2017-05-22 28109725 Fuchs O 2017-01-18 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/28109725 6q12 and 11p14 variants are associated with postnatal exhaled nitric oxide levels and respiratory symptoms. Exhaled nitric oxide output 229 European ancestry infants Illumina [567864] 5 nitric oxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0005536 GCST004060 Genome-wide genotyping array 2017-05-22 28109725 Fuchs O 2017-01-18 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/28109725 6q12 and 11p14 variants are associated with postnatal exhaled nitric oxide levels and respiratory symptoms. Exhaled nitric oxide levels 229 European ancestry infants Illumina [567864] 2 nitric oxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0005536 GCST004059 Genome-wide genotyping array 2017-06-29 28348047 Li C 2017-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28348047 Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians. Systolic blood pressure (long-term average) 18,422 East Asian ancestry individuals up to 46,629 European ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 4 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST004257 Genome-wide genotyping array 2017-06-29 28348047 Li C 2017-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28348047 Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians. Diastolic blood pressure (long-term average) 18,422 East Asian ancestry individuals up to 46,629 European ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 3 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST004258 Genome-wide genotyping array 2017-06-29 28348047 Li C 2017-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28348047 Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians. Pulse pressure (long-term average) 18,422 East Asian ancestry individuals up to 46,629 European ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 0 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST004260 Genome-wide genotyping array 2017-06-29 28348047 Li C 2017-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/28348047 Genome-Wide Association Study Meta-Analysis of Long-Term Average Blood Pressure in East Asians. Mean arterial pressure (long-term average) 18,422 East Asian ancestry individuals up to 46,629 European ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 4 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST004259 Genome-wide genotyping array 2016-12-13 26915486 Adams JN 2016-02-23 Gene www.ncbi.nlm.nih.gov/pubmed/26915486 Genetic analysis of advanced glycation end products in the DHS MIND study. Advanced glycation end-product levels 399 diabetes cases, 107 non-diabetes controls from 240 families NA Affymetrix [371951] 5 advanced glycation end-product measurement, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0007819, http://purl.obolibrary.org/obo/MONDO_0005148 GCST003457 Genome-wide genotyping array 2017-06-27 28352666 Liu TC 2017-03-23 JCI Insight www.ncbi.nlm.nih.gov/pubmed/28352666 LRRK2 but not ATG16L1 is associated with Paneth cell defect in Japanese Crohn's disease patients. Paneth cell defects in Crohn's disease 98 Japanese ancestry cases NA Affymetrix [4198245] (imputed) 9 abnormal paneth cell measurement http://www.ebi.ac.uk/efo/EFO_0007963 GCST004251 Genome-wide genotyping array 2016-11-28 26921259 Baurley JW 2016-02-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/26921259 Smokescreen: a targeted genotyping array for addiction research. Nicotine metabolite ratio 49 African American ancestry individuals, 51 Asian American ancestry individuals, 215 European American individuals NA Affymetrix [646247] 1 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST003376 Genome-wide genotyping array 2017-06-21 28322352 Ran S 2017-03-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28322352 Gene-based genome-wide association study identified 19p13.3 for lean body mass. Lean body mass 1,000 European ancestry individuals 2,283 European ancestry individuals Affymetrix [up to 379319] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST004218 Genome-wide genotyping array 2017-06-14 28295283 Wang H 2017-03-13 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/28295283 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans. Colorectal cancer 1,894 African American ancestry cases, 4,703 African American ancestry controls. 891 African American ancestry cases, 1,150 African American ancestry controls, 1,611 Hispanic ancestry cases, 4,330 Hispanic ancestry controls. Illumina [10050748] (imputed) 2 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST004168 Genome-wide genotyping array 2017-06-14 28295283 Wang H 2017-03-13 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/28295283 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans. Rectal cancer 443 African American ancestry cases, 4,703 African American ancestry controls. 284 African American ancestry cases, 1,150 African American ancestry controls Illumina [10050748] (imputed) 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST004169 Genome-wide genotyping array 2017-06-14 28295283 Wang H 2017-03-13 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/28295283 Novel colon cancer susceptibility variants identified from a genome-wide association study in African Americans. Colon cancer 1,451 African American ancestry cases, 4,703 African American ancestry controls. 607 African American ancestry cases, 1,146 African American ancestry controls. Illumina [10050748] (imputed) 2 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST004167 Genome-wide genotyping array 2017-03-20 27623749 Hwang JY 2016-09-14 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27623749 An integrative study identifies KCNC2 as a novel predisposing factor for childhood obesity and the risk of diabetes in the Korean population. Body mass index 484 Korean ancestry children 10,390 Korean ancestry individuals Illumina [357789] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST003789 Genome-wide genotyping array 2017-03-24 27670767 Chang SW 2016-09-27 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/27670767 Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes. Diabetes in response to antihypertensive drug treatment (treatment strategy interaction) 138 European American hypertensive cases with diabetes, 414 European American hypertensive cases without diabetes 157 Hispanic hypertensive cases with diabetes, 314 Hispanic hypertensive cases without diabetes, 39 African American hypertensive cases with diabetes, 78 African American hypertensive cases without diabetes Illumina [NR] (imputed) 3 response to antihypertensive drug, diabetes mellitus, response to beta blocker, response to calcium channel blocker http://www.ebi.ac.uk/efo/EFO_0005405, http://www.ebi.ac.uk/efo/EFO_0000400, http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0007767 GCST003797 Genome-wide genotyping array 2017-03-21 27671213 Petros Z 2016-09-26 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/27671213 Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity. Liver injury in anti-tuberculosis drug treatment 48 Ethiopian cases with liver injury, 354 Ethiopian cases without liver injury 27 Ethiopian cases with liver injury, 217 Ethiopian cases without liver injury Illumina [660206] 2 response to rifampicin, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007866, http://www.ebi.ac.uk/efo/EFO_0004228 GCST003792 Genome-wide genotyping array 2017-01-09 27126917 Spada J 2016-04-29 J Sleep Res www.ncbi.nlm.nih.gov/pubmed/27126917 Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study. Daytime sleep phenotypes 874 European ancestry individuals NA Affymetrix [7141204] (imputed) 101 daytime rest measurement http://www.ebi.ac.uk/efo/EFO_0007828 GCST003518 Genome-wide genotyping array 2017-01-16 27126917 Spada J 2016-04-29 J Sleep Res www.ncbi.nlm.nih.gov/pubmed/27126917 Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study. Night sleep phenotypes 941 European ancestry individuals NA Affymetrix [7141204] (imputed) 210 sleep duration, nighttime rest measurement, sleep quality, sleep latency http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0007827, http://www.ebi.ac.uk/efo/EFO_0005272, http://www.ebi.ac.uk/efo/EFO_0005280 GCST003542 Genome-wide genotyping array 2017-07-21 28416822 Low SK 2017-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28416822 Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. Atrial fibrillation 8,180 Japanese ancestry cases, 28,612 Japanese ancestry controls 3,120 Japanese ancestry cases, 125,064 Japanese ancestry controls, 15,993 European ancestry cases, 113,719 European ancestry controls Illumina [5018049] (imputed) 19 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST004373 Genome-wide genotyping array 2017-06-20 28415562 Li X 2017-03-18 Oncotarget www.ncbi.nlm.nih.gov/pubmed/28415562 Genome-wide association study of high-altitude pulmonary edema in a Han Chinese population. High-altitude pulmonary edema 68 Han Chinese ancestry cases, 84 Han Chinese controls. 199 Han Chinese ancestry cases, 304 Han Chinese controls. Affymetrix [502689] 0 high altitude pulmonary edema http://www.ebi.ac.uk/efo/EFO_1002002 GCST004200 Genome-wide genotyping array 2017-03-31 27702941 Cornelis MC 2016-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27702941 Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Caffeine metabolism (plasma 1,3,7-trimethyluric acid level) 3,562 European ancestry individuals Illumina [~ 31000000] (imputed) 0 caffeine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007872 GCST003850 Genome-wide genotyping array 2017-03-31 27702941 Cornelis MC 2016-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27702941 Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Caffeine metabolism (plasma 1,7-dimethylxanthine (paraxanthine) level) 5,353 European ancestry individuals 833 European ancestry individuals Illumina [~ 31000000] (imputed) 2 caffeine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007872 GCST003847 Genome-wide genotyping array 2017-03-31 27702941 Cornelis MC 2016-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27702941 Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Caffeine metabolism (plasma 3,7-dimethylxanthine (theobromine) level) 8,911 European ancestry individuals 824 European ancestry individuals Illumina [~ 31000000] (imputed) 1 caffeine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007872 GCST003849 Genome-wide genotyping array 2017-03-31 27702941 Cornelis MC 2016-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27702941 Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Caffeine metabolism (plasma 1,3,7-trimethylxanthine (caffeine) level) 9,054 European ancestry individuals 822 European ancestry individuals Illumina [~ 31000000] (imputed) 11 caffeine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007872 GCST003846 Genome-wide genotyping array 2017-03-31 27702941 Cornelis MC 2016-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27702941 Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Caffeine metabolism (plasma 1,3-dimethylxanthine (theophylline) level) 5,261 European ancestry individuals 826 European ancestry individuals Illumina [~ 31000000] (imputed) 4 caffeine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007872 GCST003848 Genome-wide genotyping array 2017-03-31 27702941 Cornelis MC 2016-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27702941 Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior. Caffeine metabolism (plasma 1,7-dimethylxanthine (paraxanthine) to 1,3,7-trimethylxanthine (caffeine) ratio) 5,323 European ancestry individuals 824 European ancestry individuals Illumina [~ 31000000] (imputed) 31 caffeine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007872 GCST003851 Genome-wide genotyping array 2017-05-30 28044437 McDonald MN 2017-01-02 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/28044437 Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. Body mass index (change over time) in gastrointestinal cancer or chronic obstructive pulmonary disease 237 COPD cases, 204 GI cancer cases NA Affymetrix [418365] 4 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST004100 Genome-wide genotyping array 2017-05-30 28044437 McDonald MN 2017-01-02 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/28044437 Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. Body mass index (change over time) in cancer or chronic obstructive pulmonary disease 1,085 cancer cases, 237 COPD cases NA Affymetrix [418365] 3 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST004103 Genome-wide genotyping array 2017-05-30 28044437 McDonald MN 2017-01-02 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/28044437 Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. Body mass index (change over time) in lung cancer 112 cases NA Affymetrix [418365] 3 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST004104 Genome-wide genotyping array 2017-05-30 28044437 McDonald MN 2017-01-02 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/28044437 Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. Body mass index (change over time) in gastrointestinal cancer 204 cases NA Affymetrix [418365] 3 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST004101 Genome-wide genotyping array 2017-05-30 28044437 McDonald MN 2017-01-02 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/28044437 Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. Body mass index (change over time) in chronic obstructive pulmonary disease 237 cases NA Affymetrix [418365] 6 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST004105 Genome-wide genotyping array 2017-05-30 28044437 McDonald MN 2017-01-02 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/28044437 Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. Body mass index (change over time) in lung cancer or chronic obstructive pulmonary disease 112 lung cancer cases, 237 COPD cases NA Affymetrix [418365] 5 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST004102 Genome-wide genotyping array 2017-05-30 28044437 McDonald MN 2017-01-02 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/28044437 Body mass index change in gastrointestinal cancer and chronic obstructive pulmonary disease is associated with Dedicator of Cytokinesis 1. Body mass index (change over time) in cancer 1,085 cases NA Affymetrix [418365] 1 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST004106 Genome-wide genotyping array 2017-03-16 27797806 Muller SH 2016-10-20 Brain www.ncbi.nlm.nih.gov/pubmed/27797806 Genome-wide association study in essential tremor identifies three new loci. Essential tremor 1,778 European ancestry cases, 5,376 European ancestry controls 1,029 European ancestry cases, 1,065 European ancestry controls Affymetrix [at least 416462] (imputed) 12 essential tremor http://www.ebi.ac.uk/efo/EFO_0003108 GCST003762 Genome-wide genotyping array 2017-02-24 27663945 Middeldorp CM 2016-08-05 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/27663945 A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts. Attention deficit hyperactivity disorder symptom score 17,666 children NA Affymetrix, Illumina [at least 5260671] (imputed) 9 ADHD symptom measurement http://www.ebi.ac.uk/efo/EFO_0007860 GCST003657 Genome-wide genotyping array 2017-05-15 27790247 He L 2016-11-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/27790247 Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. Age-related diseases and mortality 9,618 European ancestry individuals 19,796 European ancestry individuals Affymetrix [NR] 14 heart failure, diabetes mellitus, stroke, atrial fibrillation, mortality, coronary artery disease, cancer http://www.ebi.ac.uk/efo/EFO_0003144, http://www.ebi.ac.uk/efo/EFO_0000400, http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0000275, http://www.ebi.ac.uk/efo/EFO_0004352, http://www.ebi.ac.uk/efo/EFO_0001645, http://purl.obolibrary.org/obo/MONDO_0004992 GCST004044 Genome-wide genotyping array 2017-05-15 27790247 He L 2016-11-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/27790247 Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. Age-related diseases, mortality and associated endophenotypes 9,618 European ancestry individuals 19,796 European ancestry individuals Affymetrix [NR] 44 total cholesterol measurement, hematocrit, stroke, ventricular rate measurement, body mass index, atrial fibrillation, high density lipoprotein cholesterol measurement, coronary artery disease, diastolic blood pressure, triglyceride measurement, systolic blood pressure, heart failure, diabetes mellitus, glucose measurement, mortality, cancer http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0007928, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0000275, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0001645, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003144, http://www.ebi.ac.uk/efo/EFO_0000400, http://www.ebi.ac.uk/efo/EFO_0004468, http://www.ebi.ac.uk/efo/EFO_0004352, http://purl.obolibrary.org/obo/MONDO_0004992 GCST004045 Genome-wide genotyping array 2017-05-15 27790247 He L 2016-11-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/27790247 Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. Age-related disease endophenotypes 9,618 European ancestry individuals 19,796 European ancestry individuals Affymetrix [NR] 31 total cholesterol measurement, diastolic blood pressure, triglyceride measurement, systolic blood pressure, hematocrit, ventricular rate measurement, glucose measurement, body mass index, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0007928, http://www.ebi.ac.uk/efo/EFO_0004468, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004612 GCST004046 Genome-wide genotyping array 2017-06-22 28300201 Hernandez-Pacheco N 2017-03-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28300201 Identification of a novel locus associated with skin colour in African-admixed populations. Skin pigmentation 285 Puerto Rican individuals 373 African American individuals Affymetrix [14000000] (imputed) 42 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST004219 Genome-wide genotyping array 2017-07-13 28416812 Yang L 2017-04-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28416812 A new locus regulating MICALL2 expression was identified for association with executive inhibition in children with attention deficit hyperactivity disorder. Executive inhibition (Stroop WIT and CIT) in attention deficit hyperactivity disorder up to 780 Han Chinese ancestry child or adolescent individuals up to 922 Han Chinese ancestry child or adolescent individuals Affymetrix [at least 644166] (imputed) 1 cognitive inhibition measurement http://www.ebi.ac.uk/efo/EFO_0007969 GCST004336 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. Total cholesterol levels 22,814 East Asian ancestry individuals 57,490 East Asian ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 16 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST004231 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. LDL cholesterol levels 32,285 East Asian ancestry individuals, 173,082 European ancestry individuals 8,478 Chinese ancestry individuals Affymetrix, Illumina [~ 1900000] (imputed) 66 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST004233 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. HDL cholesterol levels 25,169 East Asian ancestry individuals 45,953 East Asian ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 18 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST004234 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. Total cholesterol levels 32,576 East Asian ancestry individuals, 187,365 European ancestry individuals 10,855 Chinese ancestry individuals Affymetrix, Illumina [up to 1900000] (imputed) 81 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST004235 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. LDL cholesterol levels 22,526 East Asian ancestry individuals 37,842 East Asian ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 13 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST004236 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. Triglyceride levels 28,183 East Asian ancestry individuals, 177,861 European ancestry individuals 10,857 Chinese ancestry individuals Affymetrix, Illumina [up to 1900000] (imputed) 49 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST004237 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. Triglyceride levels 18,421 East Asian ancestry individuals 38,060 East Asian ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST004238 Genome-wide genotyping array 2017-06-26 28334899 Spracklen CN 2017-02-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334899 Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. HDL cholesterol levels 34,930 East Asian ancestry individuals, 187,167 European ancestry individuals 8,741 Chinese ancestry individuals Affymetrix, Illumina [~ 1900000] (imputed) 90 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST004232 Genome-wide genotyping array 2017-06-27 28322246 McLaughlin RL 2017-03-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28322246 Genetic correlation between amyotrophic lateral sclerosis and schizophrenia. Amyotrophic lateral sclerosis or schizophrenia (pleiotropy) 10,147 European ancestry amyotrophic lateral sclerosis cases, 34,241 European and Asian ancestry schizophrenia cases, 22,094 European ancestry controls, 45,604 European and Asian ancestry controls NA NR [6843670] 0 amyotrophic lateral sclerosis, schizophrenia http://purl.obolibrary.org/obo/MONDO_0004976, http://purl.obolibrary.org/obo/MONDO_0005090 GCST004252 Genome-wide genotyping array 2017-06-23 28355295 Hong EP 2017-03-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/28355295 Risk prediction of pulmonary tuberculosis using genetic and conventional risk factors in adult Korean population. Tuberculosis 467 Korean ancestry cases, 1,313 Korean ancestry controls 179 Korean ancestry cases, 500 Korean ancestry controls Affymetrix [~ 4750000] (imputed) 1 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST004226 Genome-wide genotyping array 2017-03-16 27670397 Reyes-Gibby CC 2016-09-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27670397 Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients. Pre-treatment pain in head and neck squamous cell carcinoma 148 European ancestry cases, 810 European ancestry controls 58 European ancestry cases, 352 European ancestry controls Illumina [714494] 9 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST003760 Genome-wide genotyping array 2017-03-09 27665939 Liang KH 2016-09-26 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27665939 UGT2B28 genomic variation is associated with hepatitis B e-antigen seroconversion in response to antiviral therapy. Hepatitis B (viral clearance) 27 Asian ancestry delayed seroconversion cases, 30 Asian ancestry spontaneously recovered controls 192 Asian ancestry delayed seroconversion cases, 110 Asian ancestry spontaneously recovered controls Affymetrix [478372] 0 seroconversion, hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0007851, http://www.ebi.ac.uk/efo/EFO_0004197 GCST003718 Genome-wide genotyping array 2017-03-09 27656889 Alemany S 2016-09-22 PLoS One www.ncbi.nlm.nih.gov/pubmed/27656889 A Genome-Wide Association Study of Attention Function in a Population-Based Sample of Children. Attention function 1,655 European ancestry children 546 European ancestry children Illumina [240103] 0 attention function measurement http://www.ebi.ac.uk/efo/EFO_0007636 GCST003719 Genome-wide genotyping array 2017-02-03 27197191 Fehringer G 2016-04-20 Cancer Res www.ncbi.nlm.nih.gov/pubmed/27197191 Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. Cancer (pleiotropy) 5,020 European ancestry lung cancer cases, 3,718 European ancestry lung adenocarcinoma cases, 3,422 European ancestry lung squamous cell carcinoma cases, 15,414 European ancestry colorectal cancer cases, 10,809 European ancestry breast cancer cases, 4,939 European ancestry estrogen receptor negative breast cancer cases, 1,098 European ancestry ovarian cancer cases, 2,556 European ancestry serous ovarian cancer cases, 715 European ancestry ovarian endometrioid carcinoma cases, 9,710 European ancestry prostate cancer cases, 4,450 European ancestry aggressive prostate cancer cases, 61,820 European ancestry controls NA Affymetrix, Illumina [9916564] (imputed) 26 lung carcinoma, estrogen-receptor negative breast cancer, ovarian endometrioid carcinoma, colorectal cancer, prostate carcinoma, ovarian serous carcinoma, breast carcinoma, ovarian carcinoma, lung adenocarcinoma, squamous cell lung carcinoma, cancer http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_1001515, http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0001663, http://www.ebi.ac.uk/efo/EFO_1001516, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0001075, http://www.ebi.ac.uk/efo/EFO_0000571, http://www.ebi.ac.uk/efo/EFO_0000708, http://purl.obolibrary.org/obo/MONDO_0004992 GCST003588 Genome-wide genotyping array 2017-02-03 27197191 Fehringer G 2016-04-20 Cancer Res www.ncbi.nlm.nih.gov/pubmed/27197191 Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations. Cancer 5,020 European ancestry lung cancer cases, 3,718 European ancestry lung adenocarcinoma cases, 3,422 European ancestry lung squamous cell carcinoma cases, 15,414 European ancestry colorectal cancer cases, 10,809 European ancestry breast cancer cases, 4,939 European ancestry estrogen receptor negative breast cancer cases, 1,098 European ancestry ovarian cancer cases, 2,556 European ancestry serous ovarian cancer cases, 715 European ancestry ovarian endometrioid carcinoma cases, 9,710 European ancestry prostate cancer cases, 4,450 European ancestry aggressive prostate cancer cases, 61,820 European ancestry controls NA Affymetrix, Illumina [9916564] (imputed) 17 lung carcinoma, estrogen-receptor negative breast cancer, ovarian endometrioid carcinoma, colorectal cancer, prostate carcinoma, ovarian serous carcinoma, breast carcinoma, ovarian carcinoma, lung adenocarcinoma, squamous cell lung carcinoma, cancer http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_1001515, http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0001663, http://www.ebi.ac.uk/efo/EFO_1001516, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0001075, http://www.ebi.ac.uk/efo/EFO_0000571, http://www.ebi.ac.uk/efo/EFO_0000708, http://purl.obolibrary.org/obo/MONDO_0004992 GCST003587 Genome-wide genotyping array 2017-02-10 27001664 Yoo J 2016-03-21 Eur J Appl Physiol www.ncbi.nlm.nih.gov/pubmed/27001664 Genetic polymorphisms to predict gains in maximal O2 uptake and knee peak torque after a high intensity training program in humans. Maximal oxygen uptake response 79 Korean ancestry individuals NA Illumina [1131703] 0 maximal oxygen uptake measurement http://www.ebi.ac.uk/efo/EFO_0004887 GCST003608 Genome-wide genotyping array 2017-02-10 27001664 Yoo J 2016-03-21 Eur J Appl Physiol www.ncbi.nlm.nih.gov/pubmed/27001664 Genetic polymorphisms to predict gains in maximal O2 uptake and knee peak torque after a high intensity training program in humans. knee peak torque response 79 Korean ancestry individuals NA Illumina [1131703] 0 knee peak torque measurement http://www.ebi.ac.uk/efo/EFO_0007854 GCST003607 Genome-wide genotyping array 2017-02-25 27286809 Ligthart S 2016-06-10 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/27286809 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. C-reactive protein levels or triglyceride levels (pleiotropy) 65,000 individuals (C-reactive protein), 96,598 individuals (triglycerides) NA NR [25015711] (imputed) 21 triglyceride measurement, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004458 GCST003681 Genome-wide genotyping array 2017-02-25 27286809 Ligthart S 2016-06-10 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/27286809 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. C-reactive protein levels or HDL-cholesterol levels (pleiotropy) 65,000 individuals (C-reactive protein), 99,900 individuals (HDL-cholesterol) NA NR [2501543] (imputed) 20 C-reactive protein measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0004612 GCST003680 Genome-wide genotyping array 2017-02-25 27286809 Ligthart S 2016-06-10 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/27286809 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. C-reactive protein levels or LDL-cholesterol levels (pleiotropy) 65,000 individuals (C-reactive protein), 95,454 individuals (LDL-cholesterol) NA NR [2501749] (imputed) 21 low density lipoprotein cholesterol measurement, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004458 GCST003679 Genome-wide genotyping array 2017-02-25 27286809 Ligthart S 2016-06-10 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/27286809 Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation. C-reactive protein levels or total cholesterol levels (pleiotropy) 65,000 individuals (C-reactive protein), 100,184 individuals (total cholesterol) NA NR [2501549] (imputed) 20 total cholesterol measurement, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004458 GCST003678 Genome-wide genotyping array 2017-02-02 26656879 Yu H 2015-12-09 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/26656879 Genome-Wide Association Study Suggested the PTPRD Polymorphisms Were Associated With Weight Gain Effects of Atypical Antipsychotic Medications. Antipsychotic drug-induced weight gain in schizophrenia 534 Han Chinese ancestry individuals 547 East Asian ancestry individuals Illumina [495371] 0 antipsychotic drug related weight gain http://www.ebi.ac.uk/efo/EFO_0004567 GCST003579 Genome-wide genotyping array 2017-05-09 28008999 Ostrowski J 2016-12-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28008999 Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population. Crohn's disease 353 Polish ancestry child cases, 237 Polish ancestry adult cases, 582 Polish ancestry controls 71 Polish ancestry child cases, 100 Polish ancestry adult cases, 352 Polish ancestry controls Illumina [2612357] 9 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST003959 Genome-wide genotyping array 2017-05-09 28008999 Ostrowski J 2016-12-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28008999 Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population. Ulcerative colitis 269 Polish ancestry child cases, 259 Polish ancestry adult cases, 582 Polish ancestry controls 121 Polish ancestry child cases, 85 Polish ancestry adult cases, 352 Polish ancestry controls Illumina [2612357] 9 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST003960 Genome-wide genotyping array 2017-05-09 28008999 Ostrowski J 2016-12-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28008999 Genetic architecture differences between pediatric and adult-onset inflammatory bowel diseases in the Polish population. Inflammatory bowel disease 622 Polish ancestry child cases, 496 Polish ancestry adult cases, 582 Polish ancestry controls 192 Polish ancestry child cases, 185 Polish ancestry adult cases, 352 Polish ancestry controls Illumina [2612357] 18 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST003958 Genome-wide genotyping array 2017-06-29 28207573 Backman JD 2017-04-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/28207573 Genome-wide analysis of clopidogrel active metabolite levels identifies novel variants that influence antiplatelet response. Clopidogrel active metabolite levels 513 Amish individuals NA Affymetrix [7884700] (imputed) 27 clopidogrel metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007966 GCST004264 Genome-wide genotyping array 2017-06-29 28207573 Backman JD 2017-04-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/28207573 Genome-wide analysis of clopidogrel active metabolite levels identifies novel variants that influence antiplatelet response. Response to clopidogrel therapy 513 Amish individuals NA Affymetrix [7884700] (imputed) 1 platelet reactivity measurement, response to clopidogrel http://www.ebi.ac.uk/efo/EFO_0004985, http://purl.obolibrary.org/obo/GO_1903493 GCST004266 Genome-wide genotyping array 2017-03-22 27669169 Chang IS 2016-09-26 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/27669169 Genetic Modifiers of Progression-Free Survival in Never-Smoking Lung Adenocarcinoma Patients Treated with First-Line Tyrosine Kinase Inhibitors. Progression free survival in EGFR-mutation-positive never-smoking lung adenocarcinoma treated with gefitinib or erlotinib 128 Chinese ancestry cases 153 cases, 70 Chinese ancestry cases Illumina [418580] 0 progression free survival, response to gefitinib, response to erlotinib, lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0004920, http://www.ebi.ac.uk/efo/EFO_0007867, http://www.ebi.ac.uk/efo/EFO_0007868, http://www.ebi.ac.uk/efo/EFO_0000571 GCST003794 Genome-wide genotyping array 2016-12-05 27207532 Roshandel D 2016-04-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/27207532 New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins. Skin fluorescence in type 1 diabetes 1,359 European ancestry cases NA Illumina [7735748] (imputed) 1 skin fluorescence measurement http://www.ebi.ac.uk/efo/EFO_0005766 GCST003418 Genome-wide genotyping array 2017-05-23 28247064 Deming Y 2017-02-28 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/28247064 Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers. Cerebrospinal fluid AB1-42 levels 3,146 individuals NA Illumina [7358575] (imputed) 16 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST004069 Genome-wide genotyping array 2017-05-23 28247064 Deming Y 2017-02-28 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/28247064 Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers. Cerebrospinal P-tau181p levels 3,146 individuals NA Illumina [7358575] (imputed) 22 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST004070 Genome-wide genotyping array 2017-05-23 28247064 Deming Y 2017-02-28 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/28247064 Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers. Cerebrospinal T-tau levels 3,146 individuals NA Illumina [7358575] (imputed) 19 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST004071 Genome-wide genotyping array 2017-07-03 28235828 Traglia M 2017-04-03 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/28235828 Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. Midgestational circulating levels of organochlorine pesticides 329 Hispanic mothers, 273 European ancestry mothers, 122 Asian ancestry mothers, 23 South Asian ancestry mothers, 21 African American mothers, 22 other ancestry mothers NA Affymetrix [629686] 2 gestational serum measurement, organochlorine pesticide measurement http://www.ebi.ac.uk/efo/EFO_0007964, http://www.ebi.ac.uk/efo/EFO_0007960 GCST004281 Genome-wide genotyping array 2017-07-03 28235828 Traglia M 2017-04-03 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/28235828 Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. Midgestational circulating levels of PCBs (fetal genetic effect) 764 fetuses NA Affymetrix [622716] 11 polychlorinated biphenyls measurement, gestational serum measurement, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007042, http://www.ebi.ac.uk/efo/EFO_0007964, http://www.ebi.ac.uk/efo/EFO_0007959 GCST004284 Genome-wide genotyping array 2017-07-03 28235828 Traglia M 2017-04-03 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/28235828 Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. Midgestational circulating levels of PBDEs 329 Hispanic mothers, 273 European ancestry mothers, 122 Asian ancestry mothers, 23 South Asian ancestry mothers, 21 African American mothers, 22 other ancestry mothers NA Affymetrix [629686] 9 polybrominated biphenyl measurement, gestational serum measurement, polybrominated diphenyl ether measurement http://www.ebi.ac.uk/efo/EFO_0007961, http://www.ebi.ac.uk/efo/EFO_0007964, http://www.ebi.ac.uk/efo/EFO_0007962 GCST004285 Genome-wide genotyping array 2017-07-03 28235828 Traglia M 2017-04-03 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/28235828 Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. Midgestational circulating levels of PBDEs (fetal genetic effect) 764 fetuses NA Affymetrix [629686] 11 polybrominated biphenyl measurement, gestational serum measurement, fetal genotype effect measurement, polybrominated diphenyl ether measurement http://www.ebi.ac.uk/efo/EFO_0007961, http://www.ebi.ac.uk/efo/EFO_0007964, http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0007962 GCST004286 Genome-wide genotyping array 2017-07-03 28235828 Traglia M 2017-04-03 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/28235828 Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. Midgestational circulating levels of organochlorine pesticides (fetal genetic effect) 764 fetuses NA Affymetrix [629686] 0 gestational serum measurement, fetal genotype effect measurement, organochlorine pesticide measurement http://www.ebi.ac.uk/efo/EFO_0007964, http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0007960 GCST004282 Genome-wide genotyping array 2017-07-03 28235828 Traglia M 2017-04-03 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/28235828 Independent Maternal and Fetal Genetic Effects on Midgestational Circulating Levels of Environmental Pollutants. Midgestational circulating levels of PCBs 329 Hispanic mothers, 273 European ancestry mothers, 122 Asian ancestry mothers, 23 South Asian ancestry mothers, 21 African American mothers, 22 other ancestry mothers NA Affymetrix [629686] 25 polychlorinated biphenyls measurement, gestational serum measurement http://www.ebi.ac.uk/efo/EFO_0007042, http://www.ebi.ac.uk/efo/EFO_0007964 GCST004283 Genome-wide genotyping array 2017-06-15 28250457 Scerri TS 2017-02-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28250457 Genome-wide analyses identify common variants associated with macular telangiectasia type 2. Macular telangiectasia type 2 476 European ancestry cases, 1,733 European ancestry controls 172 European ancestry cases, 1,134 European ancestry controls Illumina [6310381] (imputed) 5 macular telangiectasia type 2 http://www.ebi.ac.uk/efo/EFO_1002009 GCST004171 Genome-wide genotyping array 2016-10-14 26634245 Lutz SM 2015-12-03 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26634245 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. Post bronchodilator FEV1 in COPD 5,439 European ancestry current and former smoker cases, 821 African American current and former smoker cases NA Illumina [NR] (imputed) 124 forced expiratory volume, response to bronchodilator http://www.ebi.ac.uk/efo/EFO_0004314, http://purl.obolibrary.org/obo/GO_0097366 GCST003263 Genome-wide genotyping array 2016-10-14 26634245 Lutz SM 2015-12-03 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26634245 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. Post bronchodilator FEV1/FVC ratio 10,094 European ancestry current and former smoker individuals, 3,260 African American current and former smoker individuals, 178 current and former smoker individuals NA Illumina [NR] (imputed) 1631 response to bronchodilator, FEV/FEC ratio http://purl.obolibrary.org/obo/GO_0097366, http://www.ebi.ac.uk/efo/EFO_0004713 GCST003264 Genome-wide genotyping array 2016-10-14 26634245 Lutz SM 2015-12-03 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26634245 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. Post bronchodilator FEV1 10,094 European ancestry current and former smoker individuals, 3,260 African American current and former smoker individuals, 178 current and former smoker individuals NA Illumina [NR] (imputed) 1182 forced expiratory volume, response to bronchodilator http://www.ebi.ac.uk/efo/EFO_0004314, http://purl.obolibrary.org/obo/GO_0097366 GCST003262 Genome-wide genotyping array 2016-10-14 26634245 Lutz SM 2015-12-03 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26634245 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. Post bronchodilator FEV1/FVC ratio in COPD 5,439 European ancestry current and former smoker cases, 821 African American current and former smoker cases NA Illumina [NR] (imputed) 473 response to bronchodilator, FEV/FEC ratio http://purl.obolibrary.org/obo/GO_0097366, http://www.ebi.ac.uk/efo/EFO_0004713 GCST003265 Genome-wide genotyping array 2016-10-14 26634245 Lutz SM 2015-12-03 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26634245 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. Pre bronchodilator FEV1 6,659 European ancestry current and former smoker individuals NA Illumina [NR] (imputed) 12 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST003266 Genome-wide genotyping array 2016-10-14 26634245 Lutz SM 2015-12-03 BMC Genet www.ncbi.nlm.nih.gov/pubmed/26634245 A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. Pre bronchodilator FEV1/FVC ratio 6,659 European ancestry current and former smoker individuals NA Illumina [NR] (imputed) 12 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST003267 Genome-wide genotyping array 2017-02-09 26663301 Lessard CJ 2016-05-01 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/26663301 Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans. Systemic lupus erythematosus 1,174 Korean ancestry cases, 4,246 Korean ancestry controls 739 Korean ancestry cases, 677 Chinese ancestry cases, 436 Korean ancestry controls, 709 Chinese ancestry controls Illumina [NR] 18 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST003599 Genome-wide genotyping array 2017-05-12 27927641 Ombrello MJ 2016-12-07 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/27927641 Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implications. Systemic juvenile idiopathic arthritis 178 European ancestry cases, 434 European ancestry controls, 81 Hispanic/Latin American cases, 177 Hispanic/Latin American controls, 511 cases, 6,336 controls NA Illumina [5600610] (imputed) 25 systemic juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_1001999 GCST004025 Genome-wide genotyping array 2017-02-24 26997408 Demirkan A 2016-03-21 Psychol Med www.ncbi.nlm.nih.gov/pubmed/26997408 Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies. Depressive symptoms measurement (somatic complaints domain) 1,107 Erasmus Rucphen (founder/genetic isolate) individuals, 31,421 European ancestry individuals 6,813 European ancestry individuals Affymetrix, Illumina [at least 1069063] (imputed) 1 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST003667 Genome-wide genotyping array 2017-02-24 26997408 Demirkan A 2016-03-21 Psychol Med www.ncbi.nlm.nih.gov/pubmed/26997408 Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies. Depressive symptoms measurement (lack of negative affect domain) 1,107 Erasmus Rucphen (founder/genetic isolate) individuals, 31,421 European ancestry individuals 6,813 European ancestry individuals Affymetrix, Illumina [at least 1069063] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST003669 Genome-wide genotyping array 2017-02-24 26997408 Demirkan A 2016-03-21 Psychol Med www.ncbi.nlm.nih.gov/pubmed/26997408 Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies. Depressive symptoms measurement (lack of positive affect domain) 1,107 Erasmus Rucphen (founder/genetic isolate) individuals, 31,421 European ancestry individuals 6,813 European ancestry individuals Affymetrix, Illumina [at least 1069063] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST003668 Genome-wide genotyping array 2016-12-12 27001270 Vishal M 2016-03-22 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/27001270 Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma. Glaucoma (primary open-angle) 347 Indian ancestry cases, 354 Indian ancestry controls 319 Indian ancestry cases, 297 Indian ancestry controls Illumina [521873] 5 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST003446 Genome-wide genotyping array 2017-02-13 27424934 Choi HJ 2016-07-15 Bone www.ncbi.nlm.nih.gov/pubmed/27424934 Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene. Bone mineral density (femoral neck) 2,729 Korean ancestry individuals 1,547 Han Chinese ancestry individuals, 3,237 European ancestry individuals Affymetrix [328918] 4 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST003612 Genome-wide genotyping array 2017-02-13 27424934 Choi HJ 2016-07-15 Bone www.ncbi.nlm.nih.gov/pubmed/27424934 Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene. Bone mineral density (total hip) 2,729 Korean ancestry individuals 1,547 Chinese Han ancestry individuals, 3,237 European ancestry individuals Affymetrix [328918] 4 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST003611 Genome-wide genotyping array 2017-02-13 27424934 Choi HJ 2016-07-15 Bone www.ncbi.nlm.nih.gov/pubmed/27424934 Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene. Bone mineral density (spine) 2,729 Korean ancestry individuals 1,547 Han Chinese ancestry individuals, 3,237 European ancestry individuals Affymetrix [328918] 2 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST003610 Genome-wide genotyping array 2018-09-14 27618452 Ehret GB 2016-09-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618452 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Diastolic blood pressure up to 201,529 European ancestry individuals up to 140,886 European ancestry individuals Affymetrix, Illumina, Perlegen [128272] 57 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST006258 Targeted genotyping array [CardioMetaboChip] 2018-09-14 27618452 Ehret GB 2016-09-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27618452 The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Systolic blood pressure up to 201,529 European ancestry individuals up to 140,886 European ancestry individuals Affymetrix, Illumina, Perlegen [128272] 62 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST006259 Targeted genotyping array [CardioMetaboChip] 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury (terbinafine) 14 European ancestry cases, 10,588 European ancestry controls. NA Illumina [505740] (imputed) 1 drug-induced liver injury, response to terbinafine http://www.ebi.ac.uk/efo/EFO_0004228, http://www.ebi.ac.uk/efo/EFO_0007923 GCST004078 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced hepatocellular liver injury 474 European ancestry cases, 10,588 European ancestry controls NA Illumina [505740] (imputed) 1 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST004079 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury (statins) 59 European ancestry cases, 10,588 European ancestry controls NA Illumina [505740] (imputed) 1 response to statin, drug-induced liver injury http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004080 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced cholestatic/mixed liver injury 323 European ancestry cases, 10,588 European ancestry controls. NA Illumina [505740] (imputed) 3 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST004081 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury (nitrofurantoin) 64 European ancestry cases, 10,588 European ancestry controls NA Illumina [505740] (imputed) 4 response to nitrofurantoin, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007921, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004082 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury (diclofenac) 67 European ancestry cases, 10,588 European ancestry controls NA Illumina [505740] (imputed) 4 response to diclofenac, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007919, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004083 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury (anti-tuberculosis drugs) 67 European ancestry cases, 10,588 European ancestry controls NA Illumina [505740] (imputed) 3 response to anti-tuberculosis drug, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007918, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004084 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury (fluoroquinolones) 43 European ancestry cases, 10,588 European ancestry controls NA Illumina [505740] (imputed) 4 response to fluoroquinolones, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007920, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004085 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury (nonsteroidal anti-inflammatory drugs) 144 European ancestry cases, 10,588 European ancestry controls NA Illumina [505740] (imputed) 4 response to non-steroidal anti-inflammatory, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0005533, http://www.ebi.ac.uk/efo/EFO_0004228 GCST004087 Genome-wide genotyping array 2017-05-24 28043905 Nicoletti P 2016-12-30 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28043905 Association of Liver Injury From Specific Drugs, or Groups of Drugs, With Polymorphisms in HLA and Other Genes in a Genome-Wide Association Study. Drug-induced liver injury 862 European ancestry cases and 10,588 European ancestry controls NA Illumina [505740] (imputed) 4 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST004086 Genome-wide genotyping array 2017-05-22 28095793 Chittoor G 2017-01-17 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/28095793 Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study. Glomerular load of uric acid 768 Hispanic children from 260 families Illumina [899892] 1 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST004054 Genome-wide genotyping array 2017-05-22 28095793 Chittoor G 2017-01-17 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/28095793 Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study. Uric acid clearance 768 Hispanic children from 260 families Illumina [899892] 3 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST004058 Genome-wide genotyping array 2017-05-22 28095793 Chittoor G 2017-01-17 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/28095793 Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study. Fractional excretion of uric acid 768 Hispanic children from 260 families Illumina [899892] 1 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST004055 Genome-wide genotyping array 2017-05-22 28095793 Chittoor G 2017-01-17 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/28095793 Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study. Creatinine clearance 768 Hispanic children from 260 families Illumina [899892] 1 creatinine clearance measurement http://www.ebi.ac.uk/efo/EFO_0007934 GCST004057 Genome-wide genotyping array 2017-05-22 28095793 Chittoor G 2017-01-17 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/28095793 Genetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia Study. Urinary uric acid to urinary creatinine ratio 768 Hispanic children from 260 families Illumina [899892] 2 urinary uric acid to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007935 GCST004056 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Eosinophil percentage of white cells 172,378 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 198 eosinophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007991 GCST004600 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Mean corpuscular volume 172,433 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 306 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST004602 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Platelet count 166,066 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 287 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST004603 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Hematocrit 173,039 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 133 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST004604 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Mean corpuscular hemoglobin concentration 172,851 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 84 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST004605 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Eosinophil counts 172,275 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 209 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST004606 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Plateletcrit 164,339 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 272 platelet crit http://www.ebi.ac.uk/efo/EFO_0007985 GCST004607 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Granulocyte percentage of myeloid white cells 169,545 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 220 granulocyte percentage of myeloid white cells http://www.ebi.ac.uk/efo/EFO_0007997 GCST004608 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Monocyte percentage of white cells 170,494 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 236 monocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007989 GCST004609 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. White blood cell count 172,435 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 180 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST004610 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. High light scatter reticulocyte count 170,761 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 219 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST004611 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Sum neutrophil eosinophil counts 170,384 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 154 sum of neutrophil and eosinophil counts http://www.ebi.ac.uk/efo/EFO_0009390 GCST004613 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Granulocyte count 169,822 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 155 granulocyte count http://www.ebi.ac.uk/efo/EFO_0007987 GCST004614 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. High light scatter reticulocyte percentage of red cells 170,763 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 209 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST004612 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Hemoglobin concentration 172,925 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 140 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST004615 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Platelet distribution width 164,433 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 206 platelet component distribution width http://www.ebi.ac.uk/efo/EFO_0007984 GCST004616 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Eosinophil percentage of granulocytes 170,536 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 184 eosinophil percentage of granulocytes http://www.ebi.ac.uk/efo/EFO_0007996 GCST004617 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. White blood cell count (basophil) 171,846 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 80 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST004618 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Reticulocyte fraction of red cells 170,690 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 218 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST004619 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Sum basophil neutrophil counts 170,143 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 153 sum of basophil and neutrophil counts http://www.ebi.ac.uk/efo/EFO_0009388 GCST004620 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Red cell distribution width 171,529 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 212 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST004621 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Reticulocyte count 170,641 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 210 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST004622 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Neutrophil percentage of granulocytes 170,672 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 171 neutrophil percentage of granulocytes http://www.ebi.ac.uk/efo/EFO_0007994 GCST004623 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Sum eosinophil basophil counts 171,771 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 206 sum of eosinophil and basophil counts http://www.ebi.ac.uk/efo/EFO_0009389 GCST004624 Genome-wide genotyping array 2017-08-30 27863252 Astle WJ 2016-11-17 Cell www.ncbi.nlm.nih.gov/pubmed/27863252 The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. Monocyte count 170,721 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 248 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST004625 Genome-wide genotyping array 2017-05-11 27901618 Gref A 2016-11-30 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/27901618 Genome-Wide Interaction Analysis of Air Pollution Exposure and Childhood Asthma with Functional Follow-up. Childhood onset asthma (traffic air pollution exposure interaction) 454 European ancestry child cases, 1,080 European ancestry child controls 692 European ancestry child cases, 1,096 European ancestry child controls Affymetrix, Illumina [2082301] (imputed) 0 childhood onset asthma, traffic air pollution measurement http://purl.obolibrary.org/obo/MONDO_0005405, http://www.ebi.ac.uk/efo/EFO_0007908 GCST003975 Genome-wide genotyping array 2018-04-30 28262088 Melroy-Greif WE 2017-03-06 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/28262088 Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations. Post traumatic stress disorder symptom count in trauma-exposed individuals 254 Mexican American individuals, 258 American Indian individuals NA Affymetrix [258441] (imputed) 1 response to trauma exposure, post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0008535 GCST005550 Exome genotyping array [Exome array] 2017-06-02 28256260 Siitonen A 2017-02-02 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/28256260 Genetics of early-onset Parkinson's disease in Finland: exome sequencing and genome-wide association study. Early-onset Parkinson's disease 403 Finnish ancestry cases, 1,650 Finnish ancestry controls NA NR [12954715] (imputed) 13 Young adult-onset Parkinsonism http://www.orpha.net/ORDO/Orphanet_2828 GCST004138 Genome-wide genotyping array 2017-09-20 28254843 Qi Q 2017-03-02 Diabetes www.ncbi.nlm.nih.gov/pubmed/28254843 Genetics of Type 2 Diabetes in U.S. Hispanic/Latino Individuals: Results From the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). Type 2 diabetes 2,499 Hispanic/Latino ancestry cases, 5,247 Hispanic/Latino ancestry controls Illumina [NR] (imputed) 8 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004758 Genome-wide genotyping array 2017-06-22 28253294 Vonk JM 2017-03-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/28253294 Adult onset asthma and interaction between genes and active tobacco smoking: The GABRIEL consortium. Adult onset asthma (smoking interaction) 673 European ancestry exposed cases, 651 European ancestry non-exposed cases, 1,434 European ancestry exposed controls, 1,299 European ancestry non-exposed controls 225 European ancestry exposed cases, 141 European ancestry tobacco non-exposed cases, 7,271 European ancestry exposed controls, 4,838 European ancestry non-exposed controls Illumina [at least 525150] 0 smoking behavior, adult onset asthma http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_1002011 GCST004220 Genome-wide genotyping array 2017-06-22 28253294 Vonk JM 2017-03-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/28253294 Adult onset asthma and interaction between genes and active tobacco smoking: The GABRIEL consortium. Adult onset asthma in non-smokers 651 European ancestry cases, 1,299 European ancestry controls 141 European ancestry cases, 4,838 European ancestry controls Illumina [at least 525150] 0 adult onset asthma http://www.ebi.ac.uk/efo/EFO_1002011 GCST004221 Genome-wide genotyping array 2017-06-22 28253294 Vonk JM 2017-03-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/28253294 Adult onset asthma and interaction between genes and active tobacco smoking: The GABRIEL consortium. Adult onset asthma in ever-smokers 673 European ancestry cases, 1,434 European ancestry controls 225 European ancestry cases, 7,271 European ancestry controls Illumina [at least 525150] 0 adult onset asthma http://www.ebi.ac.uk/efo/EFO_1002011 GCST004222 Genome-wide genotyping array 2017-06-23 28265120 Polimanti R 2017-03-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28265120 A genome-wide gene-by-trauma interaction study of alcohol misuse in two independent cohorts identifies PRKG1 as a risk locus. Alcohol misuse (trauma interaction) 1,748 African American trauma-exposed individuals, 643 African American trauma-unexposed individuals, 10,732 European ancestry trauma-exposed and unexposed individuals, 3,238 Hispanic trauma-exposed and unexposed individuals 2,738 African American trauma-exposed individuals, 1,591 African American trauma-unexposed individuals, 3,755 European ancestry trauma-exposed and unexposed individuals Illumina [NR] (imputed) 1 stressful life event measurement, alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007781, http://www.ebi.ac.uk/efo/EFO_0007835 GCST004225 Genome-wide genotyping array 2017-04-21 28025368 Janicki PK 2016-06-10 Pain Med www.ncbi.nlm.nih.gov/pubmed/28025368 Analysis of Common Single Nucleotide Polymorphisms in Complex Regional Pain Syndrome: Genome Wide Association Study Approach and Pooled DNA Strategy. Complex regional pain syndrome 115 cases, 115 controls 115 cases, 115 controls Illumina [200251] 0 complex regional pain syndrome http://www.ebi.ac.uk/efo/EFO_1001998 GCST003930 Genome-wide genotyping array 2017-02-14 26239289 Nelson EC 2015-08-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/26239289 Evidence of CNIH3 involvement in opioid dependence. Opioid dependence 1,167 European ancestry opioid-dependent daily injector cases, 161 European ancestry opioid misusers (impeded progression) controls 833 European ancestry opioid-dependent daily injector cases, 476 European ancestry opioid misusers (impeded progression) controls Illumina [470296] 1 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST003614 Genome-wide genotyping array 2017-05-26 28128768 Ferrari R 2017-01-23 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/28128768 Effects of Multiple Genetic Loci on Age at Onset in Frontotemporal Dementia. Frontotemporal dementia (age at onset) 411 Italian ancestry cases NA Illumina [~ 2500000] (imputed) 1 age of onset of frontotemporal dementia http://purl.obolibrary.org/obo/OBA_2001022 GCST004096 Genome-wide genotyping array 2017-05-12 28011674 Ruhle F 2016-12-23 Blood www.ncbi.nlm.nih.gov/pubmed/28011674 Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism. Venous thromboembolism 212 European ancestry trios NA Illumina [529944] 2 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST004012 Genome-wide genotyping array 2017-04-21 28011148 Zhang M 2016-12-21 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/28011148 A Genome-Wide Association Study of Basal Transepidermal Water Loss Finds that Variants at 9q34.3 Are Associated with Skin Barrier Function. Trans-epidermal water loss 611 Han Chinese ancestry individuals 366 Han Chinese ancestry individuals Illumina [7998413] (imputed) 1 skin barrier function measurement http://www.ebi.ac.uk/efo/EFO_0007891 GCST003940 Genome-wide genotyping array 2017-06-26 28371326 Zhu Y 2017-03-30 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/28371326 Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. Metabolic syndrome 862 Han Chinese ancestry cases, 880 Han Chinese ancestry controls 5,514 Han Chinese ancestry cases, 5,464 Han Chinese ancestry controls Illumina [4642479] (imputed) 2 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST004239 Genome-wide genotyping array 2017-06-26 28371326 Zhu Y 2017-03-30 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/28371326 Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. Fasting blood glucose 862 Han Chinese ancestry cases, 880 Han Chinese ancestry controls 656 Han Chinese ancestry cases, 933 Han Chinese ancestry controls Illumina [4642479] (imputed) 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST004240 Genome-wide genotyping array 2017-06-26 28371326 Zhu Y 2017-03-30 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/28371326 Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. Triglyceride levels 862 Han Chinese ancestry cases, 880 Han Chinese ancestry controls 5,514 Han Chinese ancestry cases, 5,464 Han Chinese ancestry controls Illumina [4642479] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST004241 Genome-wide genotyping array 2017-06-26 28371326 Zhu Y 2017-03-30 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/28371326 Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. HDL cholesterol 862 Han Chinese ancestry cases, 880 Han Chinese ancestry controls 5,514 Han Chinese ancestry cases, 5,464 Han Chinese ancestry controls Illumina [4642479] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST004242 Genome-wide genotyping array 2017-06-26 28371326 Zhu Y 2017-03-30 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/28371326 Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. LDL cholesterol levels 862 Han Chinese ancestry cases, 880 Han Chinese ancestry controls 656 Han Chinese ancestry cases, 933 Han Chinese ancestry controls Illumina [4642479] (imputed) 2 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST004243 Genome-wide genotyping array 2017-06-26 28371326 Zhu Y 2017-03-30 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/28371326 Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. Waist-hip ratio 862 Han Chinese ancestry cases, 880 Han Chinese ancestry controls 1,365 Han Chinese ancestry cases, 2,854 Han Chinese ancestry controls Illumina [4642479] (imputed) 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST004244 Genome-wide genotyping array 2017-06-26 28371326 Zhu Y 2017-03-30 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/28371326 Susceptibility loci for metabolic syndrome and metabolic components identified in Han Chinese: a multi-stage genome-wide association study. Body mass index 862 Han Chinese ancestry cases, 880 Han Chinese ancestry controls 1,365 Han Chinese ancestry cases, 2,854 Han Chinese ancestry controls Illumina [4642479] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004245 Genome-wide genotyping array 2017-03-20 27629089 Sailer A 2016-09-14 Neurology www.ncbi.nlm.nih.gov/pubmed/27629089 A genome-wide association study in multiple system atrophy. Multiple system atrophy (pathologically confirmed) 295 European ancestry cases, 3,864 European ancestry controls NA Illumina [4903804] (imputed) 16 multiple system atrophy http://www.ebi.ac.uk/efo/EFO_1001050 GCST003783 Genome-wide genotyping array 2017-03-20 27629089 Sailer A 2016-09-14 Neurology www.ncbi.nlm.nih.gov/pubmed/27629089 A genome-wide association study in multiple system atrophy. Multiple system atrophy 918 European ancestry cases, 3,864 European ancestry controls NA Illumina [4903804] (imputed) 22 multiple system atrophy http://www.ebi.ac.uk/efo/EFO_1001050 GCST003784 Genome-wide genotyping array 2017-07-03 28334814 Zhu Z 2017-02-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334814 Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis. Adolescent idiopathic scoliosis up to 1,456 Han Chinese ancestry cases, up to 2,104 Han Chinese ancestry controls up to 4,450 Han Chinese ancestry cases, up to 6,014 Han Chinese ancestry controls Affymetrix [435183] 8 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST004288 Genome-wide genotyping array 2017-04-19 28000841 Baek SH 2016-12-14 Mol Med Rep www.ncbi.nlm.nih.gov/pubmed/28000841 Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population. Idiopathic osteonecrosis of the femoral head 217 Korean ancestry cases, 217 Korean ancestry controls NA Affymetrix [509886] 8 idiopathic osteonecrosis of the femoral head http://www.ebi.ac.uk/efo/EFO_1001930 GCST003918 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Fasting blood insulin up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST004533 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. C-reactive protein levels up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST004530 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Diastolic blood pressure up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST004531 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Fasting blood glucose up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST004532 Genome-wide genotyping array 2017-09-20 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Fasting blood insulin adjusted for BMI up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST004762 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Height up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST004534 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Mean corpuscular hemoglobin concentration up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST004543 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Mean corpuscular volume up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST004544 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Hematocrit up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST004535 Genome-wide genotyping array 2017-09-20 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Very low density lipoprotein cholesterol levels up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 3 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST004759 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Waist circumference up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST004551 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Waist circumference adjusted for body mass index up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST004552 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Weight up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST004554 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Waist-hip ratio up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST004555 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Waist-to-hip ratio adjusted for body mass index up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST004556 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Hemoglobin up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST004536 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Homeostasis model assessment of insulin resistance up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 HOMA-IR http://www.ebi.ac.uk/efo/EFO_0004501 GCST004539 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Homeostasis model assessment of insulin resistance adjusted for BMI up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 HOMA-IR http://www.ebi.ac.uk/efo/EFO_0004501 GCST004540 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Low density lipoprotein cholesterol levels up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST004541 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Mean corpuscular hemoglobin up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 2 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST004542 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Platelet count up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST004545 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Red blood cell count up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST004546 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Systolic blood pressure up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST004547 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Total cholesterol levels up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 2 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST004548 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Triglyceride levels up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST004550 Genome-wide genotyping array 2017-08-18 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. White blood cell count up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST004553 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Body mass index up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST004529 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. High density lipoprotein cholesterol levels up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST004537 Genome-wide genotyping array 2017-08-17 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Hip bone size up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 hip bone size http://www.ebi.ac.uk/efo/EFO_0004844 GCST004538 Genome-wide genotyping array 2017-09-20 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Hip bone size adjusted for BMI up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 0 BMI-adjusted hip bone size http://www.ebi.ac.uk/efo/EFO_0008038 GCST004760 Genome-wide genotyping array 2017-09-20 28548082 Southam L 2017-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28548082 Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits. Fasting blood glucose adjusted for BMI up to 1,476 Mylopotamos (founder/genetic isolate) individuals, up to 1,737 Pomak (founder/genetic isolate) individuals NA Illumina [at least 13541454] (imputed) 1 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST004761 Genome-wide genotyping array 2017-05-12 28025584 da Silva Filho MI 2016-12-27 Leukemia www.ncbi.nlm.nih.gov/pubmed/28025584 Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. Immunoglobulin light chain (AL) amyloidosis 1,229 cases, 7,526 controls NA Affymetrix, Illumina [NR] (imputed) 10 AL amyloidosis http://purl.obolibrary.org/obo/MONDO_0019438 GCST004028 Genome-wide genotyping array 2017-03-22 27798627 Barban N 2016-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27798627 Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Number of children ever born 225,230 European ancestry women, 103,909 European ancestry men NR [2400000] (imputed) 2 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST003796 Genome-wide genotyping array 2017-03-22 27798627 Barban N 2016-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27798627 Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Age at first birth 189,656 European ancestry women, 48,408 European ancestry men Illumina [2400000] (imputed) 10 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST003795 Genome-wide genotyping array 2018-08-07 27798627 Barban N 2016-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27798627 Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Number of children ever born 103,909 European ancestry men NR [2400000] (imputed) 2 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST006046 Genome-wide genotyping array 2018-08-07 27798627 Barban N 2016-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27798627 Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Number of children ever born 225,230 European ancestry women NR [2400000] (imputed) 1 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST006047 Genome-wide genotyping array 2018-08-06 27798627 Barban N 2016-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27798627 Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Age at first birth 48,408 European ancestry men Illumina [2400000] (imputed) 2 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST006044 Genome-wide genotyping array 2018-08-06 27798627 Barban N 2016-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27798627 Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Age at first birth 189,656 European ancestry women Illumina [2400000] (imputed) 10 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST006045 Genome-wide genotyping array 2017-05-11 27992416 Lane JM 2016-12-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27992416 Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits. Excessive daytime sleepiness 111,648 European ancestry individuals NA Affymetrix [up to 73355677] (imputed) 13 excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0007875 GCST003979 Genome-wide genotyping array 2017-05-11 27992416 Lane JM 2016-12-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27992416 Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits. Sleep duration 111,975 European ancestry individuals NA Affymetrix [up to 73355677] (imputed) 8 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST003980 Genome-wide genotyping array 2017-05-11 27992416 Lane JM 2016-12-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27992416 Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits. Sleep traits (multi-trait analysis) At least 112,586 European ancestry individuals NA Affymetrix [up to 73355677] (imputed) 6 sleep duration, circadian rhythm, excessive daytime sleepiness measurement, insomnia measurement http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0004354, http://www.ebi.ac.uk/efo/EFO_0007875, http://www.ebi.ac.uk/efo/EFO_0007876 GCST003982 Genome-wide genotyping array 2017-05-11 27992416 Lane JM 2016-12-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27992416 Genome-wide association analyses of sleep disturbance traits identify new loci and highlight shared genetics with neuropsychiatric and metabolic traits. Insomnia up to 12,674 European ancestry male cases, up to 19,481 European ancestry female cases, up to 16,009 European ancestry male controls, up to 10,964 European ancestry female controls, NA Affymetrix [up to 73355677] (imputed) 8 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST003981 Genome-wide genotyping array 2017-03-06 27671502 Blokland GAM 2016-09-23 Int J Psychophysiol www.ncbi.nlm.nih.gov/pubmed/27671502 Genome-wide association study of working memory brain activation. Brain activation in response to working memory task 679 European ancestry individuals 97 unknown ancestry individuals Illumina [529379] 0 memory performance, functional brain measurement, short-term memory http://www.ebi.ac.uk/efo/EFO_0004874, http://www.ebi.ac.uk/efo/EFO_0007849, http://www.ebi.ac.uk/efo/EFO_0004335 GCST003698 Genome-wide genotyping array 2016-12-06 27207650 Schmit SL 2016-04-18 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/27207650 Genome-wide association study of colorectal cancer in Hispanics. Colorectal cancer 1,611 Hispanic cases, 4,330 Hispanic controls NA Illumina [9875636] (imputed) 7 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST003420 Genome-wide genotyping array 2016-12-09 27008869 Chen MM 2016-03-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/27008869 GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer. Endometrial cancer 4,907 European ancestry cases, 11,945 European ancestry controls NA Illumina [9486271] (imputed) 4 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST003436 Genome-wide genotyping array 2017-03-20 27629369 Gao J 2016-09-15 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/27629369 Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation. Loneliness (multivariate analysis) 8,490 European ancestry individuals, 1,228 African American individuals, 867 Hispanic American individuals, 175 individuals NA Illumina [7205781] (imputed) 19 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST003773 Genome-wide genotyping array 2017-03-20 27629369 Gao J 2016-09-15 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/27629369 Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation. Loneliness 2,075 European ancestry cases, 3,875 European ancestry controls, 427 African American cases, 398 African American controls, 294 Hispanic cases, 327 Hispanic controls, 57 cases, 73 controls NA Illumina [7176022] (imputed) 22 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST003771 Genome-wide genotyping array 2017-03-20 27629369 Gao J 2016-09-15 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/27629369 Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation. Loneliness (linear analysis) 8,490 European ancestry individuals, 1,228 African American individuals, 867 Hispanic American individuals, 175 individuals NA Illumina [7205781] (imputed) 18 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST003772 Genome-wide genotyping array 2017-02-02 26599303 Cheung CL 2016-01-12 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/26599303 HLA-B*38:02:01 predicts carbimazole/methimazole-induced agranulocytosis. Antithyroid drug-induced agranulocytosis 20 Southern Chinese ancestry cases, 775 East Asian ancestry controls 4 Southern Chinese ancestry cases, 387 East Asian ancestry controls Illumina [5339940] (imputed) 1 response to thioamide, Drug-induced agranulocytosis http://www.ebi.ac.uk/efo/EFO_0007633, http://purl.obolibrary.org/obo/HP_0012235 GCST003580 Genome-wide genotyping array 2018-05-18 29471430 Tanikawa C 2018-02-17 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/29471430 GWAS Identifies Two Novel Colorectal Cancer Loci at 16q24.1 and 20q13.12. Colorectal cancer 6,692 Japanese ancestry cases, 27,178 Japanese ancestry controls 3,713 Japanese ancestry cases, 7,333 Japanese ancestry controls Illumina [6774630] (imputed) 30 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST005591 Genome-wide genotyping array 2018-04-20 29478026 Shahin MH 2018-02-24 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29478026 Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers. Heart rate response to beta blockers (atenolol monotherapy) 228 European American hypertensive individuals, 146 African American hypertensive individuals NA Illumina [at least 1100000] (imputed) 29 response to beta blocker, heart rate http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0004326 GCST005521 Genome-wide genotyping array 2018-04-20 29478026 Shahin MH 2018-02-24 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29478026 Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers. Heart rate response to beta blockers (atenolol add-on therapy) 198 European American hypertensive individuals, 127 African American hypertensive individuals NA Illumina [at least 1100000] (imputed) 33 response to beta blocker, heart rate http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0004326 GCST005520 Genome-wide genotyping array 2018-04-20 29478026 Shahin MH 2018-02-24 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29478026 Genome-Wide Association Approach Identified Novel Genetic Predictors of Heart Rate Response to β-Blockers. Heart rate response to beta blockers 426 European American hypertensive individuals, 273 African American hypertensive individuals 200 European American hypertensive individuals, 168 African American hypertensive individuals Illumina [at least 1100000] (imputed) 2 response to beta blocker, heart rate http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0004326 GCST005519 Genome-wide genotyping array 2018-03-12 29325848 Martin J 2017-12-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29325848 A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Attention deficit hyperactivity disorder (sex interaction) 14,154 European ancestry male cases, 17,948 European ancestry male controls, 4,945 European ancestry female cases, 16,246 European ancestry female controls NA Illumina [7531543] (imputed) 0 attention deficit hyperactivity disorder, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0008343 GCST005361 Genome-wide genotyping array 2018-03-12 29325848 Martin J 2017-12-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29325848 A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Sex difference in attention deficit hyperactivity disorder 14,154 European ancestry male cases, 4,945 European ancestry female cases NA Illumina [7531543] (imputed) 0 sexual dimorphism http://www.ebi.ac.uk/efo/EFO_0005951 GCST005363 Genome-wide genotyping array 2018-03-12 29325848 Martin J 2017-12-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29325848 A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Attention deficit hyperactivity disorder 14,154 European ancestry male cases, 17,948 European ancestry male controls NA Illumina [7531543] (imputed) 10 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST005362 Genome-wide genotyping array 2021-12-16 29325848 Martin J 2017-12-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29325848 A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder. Attention deficit hyperactivity disorder 4,945 European ancestry female cases, 16,246 European ancestry female controls NA Illumina [7531543] (imputed) 10 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST012597 Genome-wide genotyping array 2017-09-05 28644415 Guenard F 2017-06-23 Nutrients www.ncbi.nlm.nih.gov/pubmed/28644415 Genome-Wide Association Study of Dietary Pattern Scores. Western dietary pattern 141 individuals NA Illumina [2668805] 23 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST004640 Genome-wide genotyping array 2017-09-05 28644415 Guenard F 2017-06-23 Nutrients www.ncbi.nlm.nih.gov/pubmed/28644415 Genome-Wide Association Study of Dietary Pattern Scores. Prudent dietary pattern 141 individuals NA Illumina [2668805] 42 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST004639 Genome-wide genotyping array 2018-09-06 29413154 Shadrin AA 2017-11-26 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/29413154 Novel Loci Associated With Attention-Deficit/Hyperactivity Disorder Are Revealed by Leveraging Polygenic Overlap With Educational Attainment. Attention deficit hyperactivity disorder or educational attainment (years of education) (pleiotropy) 2,064 European and unknown ancestry ADHD trios, 896 European and unknown ancestry ADHD cases, 2,455 European and unknown ancestry controls, 328,917 European ancestry individuals with educational attainment data NA NR [at least 6393963] (imputed) 0 attention deficit hyperactivity disorder, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004784 GCST006216 Genome-wide genotyping array 2018-07-04 29453348 Chen CJ 2018-02-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29453348 ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study. Gout 747 East Asian ancestry cases, 2,071 East Asian ancestry controls NA Affymetrix [537478] 2 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST005799 Genome-wide genotyping array 2018-07-04 29453348 Chen CJ 2018-02-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29453348 ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study. Gout vs. Hyperuricemia 747 East Asian ancestry gout cases, 747 East Asian ancestry hyperuricemia cases NA Affymetrix [537478] 1 gout, hyperuricemia http://www.ebi.ac.uk/efo/EFO_0004274, http://www.ebi.ac.uk/efo/EFO_0009104 GCST005801 Genome-wide genotyping array 2018-07-04 29453348 Chen CJ 2018-02-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29453348 ABCG2 contributes to the development of gout and hyperuricemia in a genome-wide association study. Hyperuricemia 747 East Asian ancestry cases, 2,071 East Asian ancestry controls NA Affymetrix [537478] 1 hyperuricemia http://www.ebi.ac.uk/efo/EFO_0009104 GCST005802 Genome-wide genotyping array 2017-08-21 28334935 Raffield LM 2017-05-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334935 Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? Iron status biomarkers (ferritin levels) 12,375 Hispanic/Latino individuals NA Illumina [27700000] (imputed) 11 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST004573 Genome-wide genotyping array 2017-08-21 28334935 Raffield LM 2017-05-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334935 Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? Iron status biomarkers (iron levels) 12,580 Hispanic/Latino individuals NA Illumina [27700000] (imputed) 19 serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006332 GCST004570 Genome-wide genotyping array 2017-08-21 28334935 Raffield LM 2017-05-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334935 Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? Iron status biomarkers (total iron binding capacity) 12,586 Hispanic/Latino individuals NA Illumina [27700000] (imputed) 31 total iron binding capacity http://www.ebi.ac.uk/efo/EFO_0006334 GCST004571 Genome-wide genotyping array 2017-08-21 28334935 Raffield LM 2017-05-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28334935 Genome-wide association study of iron traits and relation to diabetes in the Hispanic Community Health Study/Study of Latinos (HCHS/SOL): potential genomic intersection of iron and glucose regulation? Iron status biomarkers (transferrin saturation) 12,589 Hispanic/Latino individuals NA Illumina [27700000] (imputed) 31 transferrin saturation measurement http://www.ebi.ac.uk/efo/EFO_0006333 GCST004572 Genome-wide genotyping array 2018-12-19 26272072 Jiang X 2015-08-13 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/26272072 An Immunochip-based interaction study of contrasting interaction effects with smoking in ACPA-positive versus ACPA-negative rheumatoid arthritis. ACPA-negative rheumatoid arthritis (smoking interaction) 340 European ancestry never-smoker cases, 493 European ancestry ever-smoker cases, 746 European ancestry never-smoker controls, 994 European ancestry ever-smoker controls NA Illumina [133648] (imputed) 0 rheumatoid arthritis, smoking status measurement, ACPA-negative rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0009460 GCST006807 Targeted genotyping array [ImmunoChip] 2018-10-17 26272072 Jiang X 2015-08-13 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/26272072 An Immunochip-based interaction study of contrasting interaction effects with smoking in ACPA-positive versus ACPA-negative rheumatoid arthritis. ACPA-positive rheumatoid arthritis (smoking interaction) 340 European ancestry never-smoker cases, 493 European ancestry ever-smoker cases, 746 European ancestry never-smoker controls, 994 European ancestry ever-smoker controls 187 European ancestry never-smoker cases, 421 European ancestry ever-smoker cases, 461 European ancestry never-smoker controls, 447 European ancestry ever-smoker controls Illumina [133648] (imputed) 15 rheumatoid arthritis, smoking status measurement, ACPA-positive rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0009459 GCST006410 Targeted genotyping array [ImmunoChip] 2018-03-16 29478698 Cheng Z 2018-01-11 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29478698 Genome-wide Association Study Identifies a Regulatory Variant of RGMA Associated With Opioid Dependence in European Americans. Opioid dependence 3,058 European ancestry individuals 2,014 African American individuals Illumina [at least 4700000] (imputed) 11 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST005368 Genome-wide genotyping array 2018-04-26 24387989 Mayes MD 2014-01-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24387989 Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. Diffuse cutaneous systemic sclerosis 574 European ancestry cases, 3,466 European ancestry controls 1,217 European ancestry cases, 5,935 European ancestry controls Illumina [126270] 1 diffuse scleroderma http://www.ebi.ac.uk/efo/EFO_0000404 GCST005535 Targeted genotyping array [ImmunoChip] 2018-04-26 24387989 Mayes MD 2014-01-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24387989 Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. Systemic sclerosis 671 European ancestry ACA-positive cases, 347 European ancestry ATA-positive cases, 815 European ancestry cases, 3,466 European ancestry controls 1,387 European ancestry ACA-positive cases, 896 European ancestry ATA-positive cases, 1,734 European ancestry cases, 5,935 European ancestry controls Illumina [126270] 12 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST005534 Targeted genotyping array [ImmunoChip] 2018-04-26 24387989 Mayes MD 2014-01-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24387989 Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis. Limited cutaneous systemic scleroderma 1,127 European ancestry cases, 3,466 European ancestry controls 2,507 European ancestry cases, 5,935 European ancestry controls Illumina [126270] 4 limited scleroderma http://www.ebi.ac.uk/efo/EFO_1001017 GCST005533 Targeted genotyping array [ImmunoChip] 2018-04-07 29460428 Gelernter J 2018-02-20 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/29460428 Genomewide association study of alcohol dependence and related traits in a Thai population. Alcohol dependence symptom count 1,045 Thai ancestry individuals NA Illumina [at least 4683137] (imputed) 17 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST005440 Genome-wide genotyping array 2018-04-07 29460428 Gelernter J 2018-02-20 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/29460428 Genomewide association study of alcohol dependence and related traits in a Thai population. Alcohol consumption (max-drinks) 1,045 Thai ancestry individuals NA Illumina [at least 4683137] (imputed) 11 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST005441 Genome-wide genotyping array 2018-04-07 29460428 Gelernter J 2018-02-20 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/29460428 Genomewide association study of alcohol dependence and related traits in a Thai population. Response to alcohol consumption (flushing response) 537 Thai ancestry individuals with flushing response, 508 Thai ancestry individuals without flushing response NA Illumina [at least 4683137] (imputed) 7 response to alcohol http://www.ebi.ac.uk/efo/EFO_0005526 GCST005439 Genome-wide genotyping array 2018-05-04 25014791 Govind N 2014-08-14 Mol Med www.ncbi.nlm.nih.gov/pubmed/25014791 Immunochip identifies novel, and replicates known, genetic risk loci for rheumatoid arthritis in black South Africans. Rheumatoid arthritis 263 South African Black cases and 374 South African Black controls NA Illumina [103770] 3 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST005562 Targeted genotyping array [ImmunoChip] 2018-07-04 29453196 Sato Y 2018-02-16 J Med Genet www.ncbi.nlm.nih.gov/pubmed/29453196 Genome-wide association study identifies ERBB4 on 2q34 as a novel locus associated with sperm motility in Japanese men. Sperm motility 811 Japanese ancestry males 779 Japanese ancestry males Illumina [3901256] (imputed) 1 sperm motility measurement http://www.ebi.ac.uk/efo/EFO_0008578 GCST005798 Genome-wide genotyping array 2018-03-23 29452408 Shiga Y 2018-02-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29452408 Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma. Glaucoma (primary open-angle) 3,980 Japanese ancestry cases, 18,815 Japanese ancestry controls 4,406 East Asian ancestry cases, 18,161 East Asian ancestry controls, 5,008 European ancestry cases, 35,472 European ancestry controls, 769 African American cases, 663 African American controls, 1,572 Sub-Saharan African ancestry cases, 1,374 Sub-Saharan African ancestry controls. Illumina [6109376] (imputed) 4 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST005388 Genome-wide genotyping array 2018-03-27 29449654 Gharahkhani P 2018-02-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29449654 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Open-angle glaucoma and optic cup area 3,071 European ancestry open-angle glaucoma cases, 6,750 European ancestry controls, 22,489 European ancestry individuals with optic disc data, 7,339 Asian ancestry individuals with optic disc data NA Illumina [NR] (imputed) 2 optic cup area measurement, open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0006940, http://www.ebi.ac.uk/efo/EFO_0004190 GCST005406 Genome-wide genotyping array 2018-03-27 29449654 Gharahkhani P 2018-02-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29449654 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Open-angle glaucoma and optic disc area 3,071 European ancestry open-angle glaucoma cases, 6,750 European ancestry controls, 22,504 European ancestry individuals with disc area data, 7,307 Asian ancestry individuals with disc area data NA Illumina [NR] (imputed) 0 open-angle glaucoma, optic disc area measurement http://www.ebi.ac.uk/efo/EFO_0004190, http://www.ebi.ac.uk/efo/EFO_0006937 GCST005410 Genome-wide genotyping array 2018-03-27 29449654 Gharahkhani P 2018-02-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29449654 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Open-angle glaucoma and vertical cup-disc ratio 3,071 European ancestry open-angle glaucoma cases, 6,750 European ancestry controls, 23,899 European ancestry individuals with vertical cup to disc ratio data, 8,373 Asian ancestry individuals with vertical cup to disc ratio data NA Illumina [NR] (imputed) 2 cup-to-disc ratio measurement, open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0006939, http://www.ebi.ac.uk/efo/EFO_0004190 GCST005409 Genome-wide genotyping array 2018-03-27 29449654 Gharahkhani P 2018-02-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29449654 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Open-angle glaucoma and intra-ocular pressure 3,071 European ancestry open-angle glaucoma cases, 6,750 European ancestry controls, 29,578 European ancestry individuals with intraocular pressure data, 8,352 Asian ancestry individuals with intraocular pressure data NA Illumina [NR] (imputed) 0 open-angle glaucoma, intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004190, http://www.ebi.ac.uk/efo/EFO_0004695 GCST005408 Genome-wide genotyping array 2018-03-27 29449654 Gharahkhani P 2018-02-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29449654 Analysis combining correlated glaucoma traits identifies five new risk loci for open-angle glaucoma. Glaucoma (primary open-angle) 3,071 European ancestry cases, 6,750 European ancestry controls 3,853 cases, 33,480 controls Illumina [NR] (imputed) 4 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST005407 Genome-wide genotyping array 2018-07-04 29472613 Warrier V 2018-02-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29472613 Genetic contribution to 'theory of mind' in adolescence. Theory of mind score in adolescence (Emotional Triangles Task) 4,577 European ancestry adolescents NA Illumina [8282911] (imputed) 2 theory of mind measurement http://www.ebi.ac.uk/efo/EFO_0009103 GCST005797 Genome-wide genotyping array 2018-07-04 29499414 Pei YF 2018-02-27 Bone www.ncbi.nlm.nih.gov/pubmed/29499414 Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density. Femoral neck bone mineral density up to 4,692 European ancestry individuals, up to 1,539 Han Chinese ancestry individuals, up to 849 African American individuals, up to 446 Hispanic individuals, 2,882 European ancestry whole-genome sequenced individuals, 3,549 European ancestry whole-exome sequenced individuals, 26,534 European ancestry non-array genotype imputed individuals NA Affymetrix, Illumina [7998108] (imputed) 36 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST005795 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2018-07-04 29499414 Pei YF 2018-02-27 Bone www.ncbi.nlm.nih.gov/pubmed/29499414 Joint study of two genome-wide association meta-analyses identified 20p12.1 and 20q13.33 for bone mineral density. Lumbar spine bone mineral density up to 4,692 European ancestry individuals, up to 1,539 Han Chinese ancestry individuals, up to 849 African American individuals, up to 446 Hispanic individuals, 2,882 European ancestry whole-genome sequenced individuals, 3,549 European ancestry whole-exome sequenced individuals, 26,534 European ancestry non-array genotype imputed individuals NA Affymetrix, Illumina [7998108] (imputed) 34 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST005796 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2018-05-18 29495422 Xu H 2018-02-26 J Pers Med www.ncbi.nlm.nih.gov/pubmed/29495422 A Genome-Wide Association Study of Idiopathic Dilated Cardiomyopathy in African Americans. Idiopathic dilated cardiomyopathy 662 African American cases, 1,138 African American controls NA Affymetrix [up to 27494467] (imputed) 42 idiopathic dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0009094 GCST005588 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric areal bone mineral density (radius) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 14 radius bone mineral density http://www.ebi.ac.uk/efo/EFO_0007933 GCST004176 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric bone mineral density (spine) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 15 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST004181 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric bone mineral content (femoral neck) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 13 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST004179 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric bone mineral density (femoral neck) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 17 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST004177 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric bone mineral density (hip) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 15 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST004178 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric bone mineral content (radius) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 21 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST004175 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric bone mineral content (spine) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 12 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST004182 Genome-wide genotyping array 2017-06-15 28181694 Chesi A 2017-02-09 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/28181694 A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites. Pediatric bone mineral content (hip) 488 European ancestry female children, 445 European ancestry male children 245 European ancestry female children, 241 European ancestry male children Illumina [~ 6600000] (imputed) 15 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST004180 Genome-wide genotyping array 2017-06-27 28183528 Jun GR 2017-02-06 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/28183528 Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's disease 13,100 European ancestry cases, 13,220 European ancestry controls, 1,472 African American cases, 3,511 African American controls, 951 Japanese ancestry cases, 894 Japanese ancestry controls, 51 Israeli-Arab ancestry cases, 64 Israeli-Arab ancestry controls 5,813 European ancestry cases, 20,474 European ancestry controls NR [NR] 9 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST004246 Genome-wide genotyping array 2017-06-27 28183528 Jun GR 2017-02-06 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/28183528 Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's disease (APOE e4 interaction) 8,271 European ancestry APOE e4+ cases, 3,480 European ancestry APOE e4+ controls, 4,829 European ancestry APOE e4- cases, 9,740 European ancestry APOE e4- controls, 865 African American APOE e4+ cases, 1,241 African American APOE e4+ control, 607 African American APOE 4e- cases, 2,270 African American APOE 4e- controls, 535 Japanese ancestry APOE 4e+ cases, 151 Japanese ancestry APOE 4+ controls, 416 Japanese ancestry APOE 4- cases, 743 Japanese ancestry APOE 4- controls, 51 Arab-Israeli ancestry APOE e4- cases, 64 Arab-Israeli ancestry e4- controls 3,062 European ancestry APOE e4+ cases, 8,977 European ancestry APOE e4+ controls, 2,751 European ancestry APOE e4- cases, 11,497 European ancestry APOE e4- controls NR [NR] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST004247 Genome-wide genotyping array 2017-06-27 28183528 Jun GR 2017-02-06 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/28183528 Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's disease in APOE e4+ carriers 8,271 European ancestry cases, 3,480 European ancestry controls, 865 African American cases, 1,241 African American control, 535 Japanese ancestry cases, 151 Japanese ancestry controls 3,062 European ancestry cases, 8,977 European ancestry controls NR [NR] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST004248 Genome-wide genotyping array 2017-06-27 28183528 Jun GR 2017-02-06 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/28183528 Transethnic genome-wide scan identifies novel Alzheimer's disease loci. Alzheimer's disease in APOE e4- carriers 4,829 European ancestry cases, 9,740 European ancestry controls, 607 African American cases, 2,270 African American controls, 416 Japanese ancestry cases, 743 Japanese ancestry controls, 51 Israeli-Arab ancestry cases, 64 Israeli-Arab ancestry controls 2,751 European ancestry cases, 11,497 European ancestry controls NR [NR] 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST004249 Genome-wide genotyping array 2017-03-29 27632927 Einarsdottir E 2016-09-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27632927 Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion. Otitis media 803 Finnish ancestry child cases, 2,073 Finnish ancestry controls NA Illumina [319683] 4 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST003827 Genome-wide genotyping array 2017-03-29 27632927 Einarsdottir E 2016-09-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27632927 Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion. Otitis media (chronic) 512 Finnish ancestry child cases, 2,073 Finnish ancestry controls 1,466 child cases, 3,394 controls Illumina [319683] 2 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST003828 Genome-wide genotyping array 2017-03-29 27632927 Einarsdottir E 2016-09-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/27632927 Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion. Otitis media (recurrent) 702 Finnish ancestry child cases, 2,073 Finnish ancestry controls NA Illumina [319683] 4 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST003829 Genome-wide genotyping array 2017-06-12 28194004 Deary V 2017-02-14 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28194004 Genetic contributions to self-reported tiredness. Self-reported tiredness 108,976 British ancestry individuals NA Affymetrix [~ 17300000] (imputed) 3 tiredness measurement http://www.ebi.ac.uk/efo/EFO_0007946 GCST004158 Genome-wide genotyping array 2017-06-16 28166213 Wain LV 2017-02-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28166213 Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Lung function (FEV1) 48,943 European ancestry individuals. 57,176 European ancestry individuals, 38,199 individuals. Affymetrix [up to 27624732] (imputed) 33 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST004183 Genome-wide genotyping array 2017-06-16 28166213 Wain LV 2017-02-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28166213 Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Lung function (FVC) 48,943 European ancestry individuals. 57,176 European ancestry individuals, 38,199 individuals. Affymetrix [27624732] (imputed) 20 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST004184 Genome-wide genotyping array 2017-06-16 28166213 Wain LV 2017-02-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28166213 Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets. Lung function (FEV1/FVC) 48,943 European ancestry individuals 57,176 European ancestry individuals, 38,199 individuals. Affymetrix [27624732] (imputed) 56 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST004185 Genome-wide genotyping array 2017-06-01 28107422 de Vries PS 2017-01-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/28107422 Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. Fibrinogen levels 91,953 European ancestry individuals (imputed to HapMap) Affymetrix, Illumina [2749429] (imputed) 36 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST004122 Genome-wide genotyping array 2017-06-01 28107422 de Vries PS 2017-01-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/28107422 Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study. Fibrinogen levels 91,953 European ancestry individuals (imputed to 1000 Genomes) Affymetrix, Illumina [10883314] (imputed) 36 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST004121 Genome-wide genotyping array 2017-05-23 28100913 Ueta M 2017-01-19 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28100913 Genome-wide association study using the ethnicity-specific Japonica array: identification of new susceptibility loci for cold medicine-related Stevens-Johnson syndrome with severe ocular complications. Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe ocular complications 117 Japanese ancestry cases, 688 Japanese ancestry controls 52 East Asian ancestry cases, 302 East Asian ancestry controls Affymetrix [6714496] (imputed) 3 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to cold medicine http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://www.ebi.ac.uk/efo/EFO_0006997 GCST004072 Genome-wide genotyping array 2017-06-12 28187132 Kiryluk K 2017-02-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28187132 GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway. Serum galactose-deficient IgA1 levels 950 Han Chinese ancestry individuals, 245 European ancestry individuals 653 East Asian ancestry individuals, 785 European ancestry individuals Illumina [468781] 4 serum galactose-deficient IgA1 measurement http://www.ebi.ac.uk/efo/EFO_0007947 GCST004159 Genome-wide genotyping array 2017-04-20 28011712 Foo JN 2016-12-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28011712 Genome-wide association study of Parkinson's disease in East Asians. Parkinson's disease 779 Han Chinese ancestry cases, 13,227 Han Chinese ancestry controls 5,125 Asian ancestry cases, 17,604 Asian ancestry controls Illumina [2402394] (imputed) 4 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST003922 Genome-wide genotyping array 2017-04-10 27981573 Zhong WP 2016-12-16 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/27981573 Genomewide Association Study Identifies Novel Genetic Loci That Modify Antiplatelet Effects and Pharmacokinetics of Clopidogrel. Response to clopidogrel therapy in coronary heart disease 115 Han Chinese ancestry cases NA Illumina [703143] 0 platelet reactivity measurement, response to clopidogrel http://www.ebi.ac.uk/efo/EFO_0004985, http://purl.obolibrary.org/obo/GO_1903493 GCST003899 Genome-wide genotyping array 2017-06-02 28067908 de Lange KM 2017-01-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28067908 Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. Crohn's disease 12,194 European and unknown ancestry cases, 28,072 European and unknown ancestry controls NA Illumina [9560910] (imputed) 119 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST004132 Genome-wide genotyping array 2017-06-02 28067908 de Lange KM 2017-01-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28067908 Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. Ulcerative colitis 12,366 European and unknown ancestry cases, 33,609 European and unknown ancestry controls NA Illumina [9578670] (imputed) 80 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST004133 Genome-wide genotyping array 2017-06-02 28067908 de Lange KM 2017-01-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28067908 Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. Inflammatory bowel disease 25,042 European and unknown ancestry cases, 34,915 European and unknown ancestry controls NA Illumina [9725440] (imputed) 135 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST004131 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. beta-nerve growth factor levels 3,531 Finnish ancestry individuals NA NR [10700000] (imputed) 26 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST004421 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Vascular endothelial growth factor levels 7,118 Finnish ancestry individuals NA NR [10700000] (imputed) 40 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST004422 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. CTACK levels 3,631 Finnish ancestry individuals NA NR [10700000] (imputed) 46 chemokine (C-C motif) ligand 27 measurement http://www.ebi.ac.uk/efo/EFO_0008082 GCST004420 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Eotaxin levels 8,153 Finnish ancestry individuals NA NR [10700000] (imputed) 46 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST004460 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Fibroblast growth factor basic levels 7,565 Finnish ancestry individuals NA NR [10700000] (imputed) 28 fibroblast growth factor basic measurement http://www.ebi.ac.uk/efo/EFO_0008130 GCST004459 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Granulocyte-colony stimulating factor levels 7,904 Finnish ancestry individuals NA NR [10700000] (imputed) 20 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST004458 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Growth-regulated protein alpha levels 3,505 Finnish ancestry individuals NA NR [10700000] (imputed) 26 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST004457 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Hepatocyte growth factor levels 8,292 Finnish ancestry individuals NA NR [10700000] (imputed) 25 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST004449 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interferon gamma levels 7,701 Finnish ancestry individuals NA NR [10700000] (imputed) 29 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST004456 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-1-beta levels 3,309 Finnish ancestry individuals NA NR [10700000] (imputed) 23 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST004448 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-1-receptor antagonist levels 3,638 Finnish ancestry individuals NA NR [10700000] (imputed) 22 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST004447 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-2 levels 3,475 Finnish ancestry individuals NA NR [10700000] (imputed) 26 interleukin 2 measurement http://www.ebi.ac.uk/efo/EFO_0008331 GCST004455 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-2 receptor antagonist levels 3,677 Finnish ancestry individuals NA NR [10700000] (imputed) 27 interleukin 2 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0008332 GCST004454 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-4 levels 8,124 Finnish ancestry individuals NA NR [10700000] (imputed) 24 interleukin 4 measurement http://www.ebi.ac.uk/efo/EFO_0008184 GCST004453 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-5 levels 3,364 Finnish ancestry individuals NA NR [10700000] (imputed) 17 interleukin 5 measurement http://www.ebi.ac.uk/efo/EFO_0008185 GCST004452 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-6 levels 8,189 Finnish ancestry individuals NA NR [10700000] (imputed) 29 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST004446 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-7 levels 3,409 Finnish ancestry individuals NA NR [10700000] (imputed) 23 interleukin 7 measurement http://www.ebi.ac.uk/efo/EFO_0008189 GCST004451 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-8 levels 3,526 Finnish ancestry individuals NA NR [10700000] (imputed) 18 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST004445 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-9 levels 3,634 Finnish ancestry individuals NA NR [10700000] (imputed) 25 interleukin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008192 GCST004450 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-10 levels 7,681 Finnish ancestry individuals NA NR [10700000] (imputed) 34 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST004444 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-13 levels 3,557 Finnish ancestry individuals NA NR [10700000] (imputed) 33 interleukin 13 measurement http://www.ebi.ac.uk/efo/EFO_0008171 GCST004443 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-17 levels 7,760 Finnish ancestry individuals NA NR [10700000] (imputed) 34 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST004442 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-18 levels 3,636 Finnish ancestry individuals NA NR [10700000] (imputed) 44 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST004441 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Macrophage Migration Inhibitory Factor levels 3,494 Finnish ancestry individuals NA NR [10700000] (imputed) 26 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST004423 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interferon gamma-induced protein 10 levels 3,685 Finnish ancestry individuals NA NR [10700000] (imputed) 36 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST004440 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-12p70 levels 8,270 Finnish ancestry individuals NA NR [10700000] (imputed) 36 interleukin 12 measurement http://www.ebi.ac.uk/efo/EFO_0004753 GCST004439 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Interleukin-16 levels 3,483 Finnish ancestry individuals NA NR [10700000] (imputed) 22 interleukin 16 measurement http://www.ebi.ac.uk/efo/EFO_0008173 GCST004430 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Monocyte chemoattractant protein-1 levels 8,293 Finnish ancestry individuals NA NR [10700000] (imputed) 53 CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004749 GCST004438 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Monocyte chemoattractant protein-3 levels 843 Finnish ancestry individuals NA NR [10700000] (imputed) 14 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST004437 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Macrophage colony stimulating factor levels 840 Finnish ancestry individuals NA NR [10700000] (imputed) 23 macrophage colony stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008217 GCST004436 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Monokine induced by gamma interferon levels 3,685 Finnish ancestry individuals NA NR [10700000] (imputed) 35 monokine induced by gamma interferon measurement http://www.ebi.ac.uk/efo/EFO_0008236 GCST004435 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Macrophage inflammatory protein 1a levels 3,522 Finnish ancestry individuals NA NR [10700000] (imputed) 22 macrophage inflammatory protein 1a measurement http://www.ebi.ac.uk/efo/EFO_0008218 GCST004434 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Macrophage inflammatory protein 1b levels 8,243 Finnish ancestry individuals NA NR [10700000] (imputed) 104 macrophage inflammatory protein 1b measurement http://www.ebi.ac.uk/efo/EFO_0008219 GCST004433 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Platelet-derived growth factor BB levels 8,293 Finnish ancestry individuals NA NR [10700000] (imputed) 38 platelet-derived growth factor BB measurement http://www.ebi.ac.uk/efo/EFO_0008264 GCST004432 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. RANTES levels 3,421 Finnish ancestry individuals NA NR [10700000] (imputed) 33 CCL5 measurement http://www.ebi.ac.uk/efo/EFO_0005117 GCST004431 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Stem cell factor levels 8,290 Finnish ancestry individuals NA NR [10700000] (imputed) 29 stem Cell Factor measurement http://www.ebi.ac.uk/efo/EFO_0008291 GCST004429 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Stem cell growth factor beta levels 3,682 Finnish ancestry individuals NA NR [10700000] (imputed) 53 stem Cell Growth Factor beta measurement http://www.ebi.ac.uk/efo/EFO_0008292 GCST004428 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Stromal-cell-derived factor 1 alpha levels 5,998 Finnish ancestry individuals NA NR [10700000] (imputed) 26 stromal cell-derived factor 1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0008293 GCST004427 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Tumor necrosis factor alpha levels 3,454 Finnish ancestry individuals NA NR [10700000] (imputed) 19 tumor necrosis factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0004684 GCST004426 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. Tumor necrosis factor beta levels 1,559 Finnish ancestry individuals NA NR [10700000] (imputed) 11 tumor necrosis factor beta measurement http://www.ebi.ac.uk/efo/EFO_0008308 GCST004425 Genome-wide genotyping array 2017-08-04 27989323 Ahola-Olli AV 2016-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/27989323 Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors. TRAIL levels 8,186 Finnish ancestry individuals NA NR [10700000] (imputed) 58 TNF-related apoptosis-inducing ligand measurement http://www.ebi.ac.uk/efo/EFO_0008300 GCST004424 Genome-wide genotyping array 2017-05-19 28054174 Leslie EJ 2017-01-04 Hum Genet www.ncbi.nlm.nih.gov/pubmed/28054174 Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. Cleft palate 272 Asian ancestry case-parent trios, 161 Asian ancestry controls, 38 European ancestry cases, 296 European ancestry case-parent trios, 835 European ancestry controls, 40 Latino or African cases, 34 Latino or African case-parent trios, 704 Latino or African controls, 14 case-parent trios. NA Illumina [6090031] (imputed) 7 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST004052 Genome-wide genotyping array 2017-05-19 28054174 Leslie EJ 2017-01-04 Hum Genet www.ncbi.nlm.nih.gov/pubmed/28054174 Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. Orofacial clefts 83 Asian ancestry cases, 1,445 Asian ancestry case-parent trios, 161 Asian ancestry controls, 208 European ancestry cases, 1,284 European ancestry case-parent trios, 835 European ancestry controls, 610 Latino or African cases, 663 Latino or African case-parent trios, 704 Latino or African controls, 35 case-parent trios. NA Illumina [6090031] (imputed) 24 Orofacial cleft http://purl.obolibrary.org/obo/HP_0000202 GCST004051 Genome-wide genotyping array 2017-05-19 28054174 Leslie EJ 2017-01-04 Hum Genet www.ncbi.nlm.nih.gov/pubmed/28054174 Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate. Cleft lip with or without cleft palate 83 Asian ancestry cases, 1,173 Asian ancestry case-parent trios, 161 Asian ancestry controls,170 European ancestry cases, 988 European ancestry case-parent trios, 835 European ancestry controls, 570 Latino or African cases, 629 Latino or African case-parent trios, 704 Latino or African controls, 21 case-parent trios. NA Illumina [6090031] (imputed) 32 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST004050 Genome-wide genotyping array 2017-05-11 27976721 Wang Z 2016-12-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27976721 A large-scale genome-wide association and meta-analysis identified four novel susceptibility loci for leprosy. Leprosy 2,743 Chinese ancestry cases, 3,573 Chinese ancestry controls 5,413 Han Chinese ancestry cases, 12,037 Han Chinese ancestry controls Illumina [5546030] (imputed) 13 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST004009 Genome-wide genotyping array 2017-05-26 28108127 Eitel I 2017-01-15 Int J Cardiol www.ncbi.nlm.nih.gov/pubmed/28108127 Genome-wide association study in takotsubo syndrome - Preliminary results and future directions. Takotsubo syndrome 96 European ancestry cases, 475 controls NA NR [at least 498281] (imputed) 5 Takotsubo cardiomyopathy http://www.ebi.ac.uk/efo/EFO_1002000 GCST004095 Genome-wide genotyping array 2017-05-15 28011710 Benyamin B 2016-12-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28011710 Identification of novel loci affecting circulating chromogranins and related peptides. Circulating chromogranin peptide levels up to 540 European American and Mexican American individuals, up to 1,267 individuals NA Illumina [at least 2587527] (imputed) 5 CHGB cleavage product measurement, CHGA cleavage product measurement http://www.ebi.ac.uk/efo/EFO_0007910, http://www.ebi.ac.uk/efo/EFO_0007909 GCST004038 Genome-wide genotyping array 2019-08-12 27903959 Lv H 2017-01-31 Oncotarget www.ncbi.nlm.nih.gov/pubmed/27903959 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. Core binding factor acute myeloid leukemia 175 European ancestry cases, 218 European ancestry controls NA Affymetrix [734624] 1744 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST008413 Genome-wide genotyping array 2017-07-13 28346443 Melin BS 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346443 Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Glioma 12,469 European ancestry cases, 18,190 European ancestry controls. NA Illumina [at least 6887412] (imputed) 18 central nervous system cancer, glioma http://www.ebi.ac.uk/efo/EFO_0000326, http://www.ebi.ac.uk/efo/EFO_0005543 GCST004347 Genome-wide genotyping array 2017-07-13 28346443 Melin BS 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346443 Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Non-glioblastoma glioma 5,819 European ancestry cases, 18,190 European ancestry controls. NA Illumina [at least 6769856] (imputed) 19 central nervous system cancer, glioma http://www.ebi.ac.uk/efo/EFO_0000326, http://www.ebi.ac.uk/efo/EFO_0005543 GCST004348 Genome-wide genotyping array 2017-07-13 28346443 Melin BS 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346443 Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Glioblastoma 6,191 European ancestry cases, 18,190 European ancestry controls. NA Illumina [at least 6790270] (imputed) 13 central nervous system cancer, glioblastoma multiforme http://www.ebi.ac.uk/efo/EFO_0000326, http://www.ebi.ac.uk/efo/EFO_0000519 GCST004349 Genome-wide genotyping array 2018-05-15 29472232 Li Y 2018-02-22 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/29472232 Genome-Wide Association and Functional Studies Identify SCML4 and THSD7A as Novel Susceptibility Genes for Coronary Artery Disease. Coronary artery disease 280 Han Chinese ancestry cases, 350 Han Chinese ancestry controls 9,764 Han Chinese ancestry cases, 11,434 Han Chinese ancestry controls Affymetrix [314806] (imputed) 4 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST005582 Genome-wide genotyping array 2017-07-19 28333195 Uimari O 2017-04-01 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/28333195 Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis. Endometriosis 3,194 European ancestry cases, 7,060 European ancestry controls. NA Illumina [NR] (imputed) 6 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST004368 Genome-wide genotyping array 2017-07-19 28333195 Uimari O 2017-04-01 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/28333195 Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis. Ovarian disease with few adhesions 1,686 European ancestry cases, 7,060 European ancestry controls. Illumina [NR] (imputed) 4 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST004369 Genome-wide genotyping array 2017-07-19 28333195 Uimari O 2017-04-01 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/28333195 Genome-wide genetic analyses highlight mitogen-activated protein kinase (MAPK) signaling in the pathogenesis of endometriosis. Deep ovarian and/or rectovaginal disease with dense adhesions 1,364 European ancestry cases, 7,060 European ancestry controls. NA Illumina [NR] (imputed) 10 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST004370 Genome-wide genotyping array 2017-08-16 28521775 Manichaikul A 2017-05-18 Respir Res www.ncbi.nlm.nih.gov/pubmed/28521775 Genome-wide association study of subclinical interstitial lung disease in MESA. Subclinical trait of interstitial lung disease (basilar percentage of high attenuation areas on CT scan) 2,434 European ancestry individuals, 2,470 African American individuals, 2,065 Hispanic individuals, 702 Chinese ancestry individuals 3,013 European ancestry individuals Affymetrix [at least 897981] (imputed) 4 airway imaging measurement http://www.ebi.ac.uk/efo/EFO_0007627 GCST004526 Genome-wide genotyping array 2017-08-16 28521775 Manichaikul A 2017-05-18 Respir Res www.ncbi.nlm.nih.gov/pubmed/28521775 Genome-wide association study of subclinical interstitial lung disease in MESA. Subclinical trait of interstitial lung disease (basilar peel-core ratio of high attentuation areas on CT scan) 2,434 European ancestry individuals, 2,470 African American individuals, 2,065 Hispanic individuals, 702 Chinese ancestry individuals NA Affymetrix [at least 897981] (imputed) 9 airway imaging measurement http://www.ebi.ac.uk/efo/EFO_0007627 GCST004525 Genome-wide genotyping array 2017-08-16 28521775 Manichaikul A 2017-05-18 Respir Res www.ncbi.nlm.nih.gov/pubmed/28521775 Genome-wide association study of subclinical interstitial lung disease in MESA. Subclinical trait of interstitial lung disease (percentage of high attenuation areas on CT scan) 2,434 European ancestry individuals, 2,470 African American individuals, 2,065 Hispanic individuals, 702 Chinese ancestry individuals 3,013 European ancestry individuals Affymetrix [at least 897981] (imputed) 1 airway imaging measurement http://www.ebi.ac.uk/efo/EFO_0007627 GCST004527 Genome-wide genotyping array 2019-01-21 29970889 Day FR 2018-07-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29970889 Elucidating the genetic basis of social interaction and isolation. Loneliness 80,134 European ancestry cases, 364,890 European ancestry controls NA NR [NR] (imputed) 15 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST006923 Genome-wide genotyping array 2019-01-21 29970889 Day FR 2018-07-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29970889 Elucidating the genetic basis of social interaction and isolation. Social isolation 2,426 European ancestry cases, 286,524 European ancestry controls NA NR [NR] (imputed) 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST006918 Genome-wide genotyping array 2019-01-21 29970889 Day FR 2018-07-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29970889 Elucidating the genetic basis of social interaction and isolation. Ability to confide in someone 64,505 European ancestry cases, 238,062 European ancestry controls NA NR [NR] (imputed) 4 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST006919 Genome-wide genotyping array 2019-01-21 29970889 Day FR 2018-07-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29970889 Elucidating the genetic basis of social interaction and isolation. Regular attendance at a gym or sports club 135,060 European ancestry cases, 317,242 European ancestry controls NA NR [NR] (imputed) 8 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST006920 Genome-wide genotyping array 2019-01-21 29970889 Day FR 2018-07-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29970889 Elucidating the genetic basis of social interaction and isolation. Regular attendance at a pub or social club 124,047 European ancestry cases, 328,255 European ancestry controls NA NR [NR] (imputed) 13 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST006921 Genome-wide genotyping array 2019-01-21 29970889 Day FR 2018-07-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29970889 Elucidating the genetic basis of social interaction and isolation. Regular attendance at a religious group 66,259 European ancestry cases, 386,043 European ancestry controls NA NR [NR] (imputed) 19 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST006922 Genome-wide genotyping array 2019-01-21 29970889 Day FR 2018-07-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29970889 Elucidating the genetic basis of social interaction and isolation. Loneliness (MTAG) 487,647 European ancestry individuals NA NR [NR] (imputed) 16 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST006924 Genome-wide genotyping array 2020-01-20 31272903 Sunadome H 2019-07-01 Allergol Int www.ncbi.nlm.nih.gov/pubmed/31272903 Correlation between eosinophil count, its genetic background and body mass index: The Nagahama Study. Eosinophil counts 4,650 East Asian ancestry individuals NA Illumina [103680] (imputed) 9 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST009456 Genome-wide genotyping array 2020-01-20 31272903 Sunadome H 2019-07-01 Allergol Int www.ncbi.nlm.nih.gov/pubmed/31272903 Correlation between eosinophil count, its genetic background and body mass index: The Nagahama Study. Eosinophil counts 4,206 East Asian ancestry individuals NA Illumina [103680] (imputed) 5 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST009457 Genome-wide genotyping array 2019-08-30 31264924 Meng W 2019-07-02 Ophthalmic Genet www.ncbi.nlm.nih.gov/pubmed/31264924 A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity. Diabetic maculopathy with decreased visual acuity in type 2 diabetes 469 Scottish ancestry cases, 1,374 Scottish ancestry controls NA Affymetrix, Illumina [6717712] (imputed) 2 visual acuity measurement, diabetic maculopathy http://www.ebi.ac.uk/efo/EFO_0008385, http://www.ebi.ac.uk/efo/EFO_0010133 GCST008545 Genome-wide genotyping array 2019-08-30 31264924 Meng W 2019-07-02 Ophthalmic Genet www.ncbi.nlm.nih.gov/pubmed/31264924 A genome-wide association study implicates that the TTC39C gene is associated with diabetic maculopathy with decreased visual acuity. Diabetic maculopathy in type 2 diabetes 1,240 Scottish ancestry cases, 1,374 Scottish ancestry controls NA Affymetrix, Illumina [6717712] (imputed) 8 diabetic maculopathy http://www.ebi.ac.uk/efo/EFO_0010133 GCST008546 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Decreased fine motor function in Charcot-Marie-Tooth disease 1A (eating with utensils) 132 European ancestry severe cases, 288 European ancestry mild cases NA Illumina [600000] 1 decreased fine motor function http://www.ebi.ac.uk/efo/EFO_0010132 GCST008533 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Hearing loss in Charcot-Marie-Tooth disease 1A 61 European ancestry severe cases, 303 European ancestry mild cases NA Illumina [600000] 1 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST008534 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Decreased sensory function in Charcot-Marie-Tooth disease type 1A 308 European ancestry severe cases, 112 European ancestry mild cases NA Illumina [600000] 1 Somatic sensory dysfunction http://purl.obolibrary.org/obo/HP_0003474 GCST008537 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Neuropathy in Charcot-Marie-Tooth disease type 1A 471 European ancestry individuals NA Illumina [600000] 1 neuropathy http://www.ebi.ac.uk/efo/EFO_0004149 GCST008530 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Balance difficulty in Charcot-Marie-Tooth disease type 1A 352 European ancestry severe cases, 61 European ancestry mild cases NA Illumina [600000] 1 Gait imbalance http://purl.obolibrary.org/obo/HP_0002141 GCST008538 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Decreased fine motor function in Charcot-Marie-Tooth disease 1A (buttons, zippers, fasteners, bottles) 277 European ancestry severe cases, 146 European ancestry mild cases NA Illumina [600000] 1 decreased fine motor function http://www.ebi.ac.uk/efo/EFO_0010132 GCST008540 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Walking difficulty in Charcot-Marie-Tooth disease 1A 362 European ancestry severe cases, 62 European ancestry mild cases NA Illumina [600000] 1 decreased walking ability http://www.ebi.ac.uk/efo/EFO_0010131 GCST008543 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A 174 European ancestry severe cases, 117 European ancestry mild cases NA Illumina [600000] 0 foot muscle strength measurement http://www.ebi.ac.uk/efo/EFO_0009699 GCST008544 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. First dorsal interosseous strength in Charcot-Marie-Tooth disease 1A 120 European ancestry severe cases, 80 European ancestry mild cases NA Illumina [600000] 0 foot muscle strength measurement http://www.ebi.ac.uk/efo/EFO_0009699 GCST008542 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Foot deformity in Charcot-Marie-Tooth disease 1A 368 European ancestry severe cases, 49 European ancestry mild cases NA Illumina [600000] 1 Abnormal foot morphology http://purl.obolibrary.org/obo/HP_0001760 GCST008541 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Foot plantar flexion strength in Charcot-Marie-Tooth disease 1A 136 European ancestry severe cases, 276 European ancestry mild cases NA Illumina [600000] 1 foot muscle strength measurement http://www.ebi.ac.uk/efo/EFO_0009699 GCST008539 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Scoliosis in Charcot-Marie-Tooth disease 1A 91 European ancestry severe cases, 318 European ancestry mild cases NA Illumina [600000] 1 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST008536 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Arthritic-like pain in Charcot-Marie-Tooth type 1A 197 European ancestry severe cases, 212 European ancestry mild cases NA Illumina [600000] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST008535 Genome-wide genotyping array 2019-08-29 30958311 Tao F 2019-04-03 J Neuromuscul Dis www.ncbi.nlm.nih.gov/pubmed/30958311 Modifier Gene Candidates in Charcot-Marie-Tooth Disease Type 1A: A Case-Only Genome-Wide Association Study. Burning or tingling in extremities in Charcot-Marie-Tooth disease type 1A 141 European ancestry severe cases, 265 European ancestry mild cases NA Illumina [600000] 1 disturbance of skin sensation http://www.ebi.ac.uk/efo/EFO_0009522 GCST008532 Genome-wide genotyping array 2019-08-19 31263063 Dufek S 2019-07-01 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31263063 Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome. Childhood steroid-sensitive nephrotic syndrome 422 European ancestry cases, 5,642 European ancestry controls NA Illumina [5216266] (imputed) 19 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST008456 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Diastolic blood pressure x physical activity (least active quartile vs others) interaction (2df) 1,913 European ancestry inactive individuals, 4,792 European ancestry active individuals NA NR [2144169] (imputed) 3 diastolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008412 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Diastolic blood pressure x physical activity (less vs more active half) interaction (2df) 3,495 European ancestry inactive individuals, 3,210 European ancestry active individuals NA NR [2144141] (imputed) 5 diastolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008411 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Diastolic blood pressure x physical activity (least vs most active quartile) interaction (2df) 1,913 European ancestry inactive individuals, 2,071 European ancestry active individuals NA NR [2144462] (imputed) 5 diastolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008410 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity (least active quartile vs others) interaction (2df) 1,913 European ancestry inactive individuals, 4,792 European ancestry active individuals NA NR [2144171] (imputed) 5 systolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008409 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity (less vs more active half) interaction (2df) 3,495 European ancestry inactive individuals, 3,210 European ancestry active individuals NA NR [2144143] (imputed) 15 systolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008408 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity (least vs most active quartile) interaction (2df) 1,913 European ancestry inactive individuals, 2,071 European ancestry active individuals NA NR [2144462] (imputed) 10 systolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008402 Genome-wide genotyping array 2019-08-08 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity interaction (2df) 6,705 European ancestry individuals NA NR [2144171] (imputed) 13 systolic blood pressure, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0008002 GCST008393 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Diastolic blood pressure x physical activity (least active quartile vs others) interaction (1df) 1,913 European ancestry inactive individuals, 4,792 European ancestry active individuals NA NR [2144169] (imputed) 3 diastolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008407 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Diastolic blood pressure x physical activity (less vs more active half) interaction (1df) 3,495 European ancestry inactive individuals, 3,210 European ancestry active individuals NA NR [2144141] (imputed) 9 diastolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008406 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Diastolic blood pressure x physical activity (least vs most active quartile) interaction (1df) 1,913 European ancestry inactive individuals, 2,071 European ancestry active individuals NA NR [2144462] (imputed) 8 diastolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008405 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity (least active quartile vs others) interaction (1df) 1,913 European ancestry inactive individuals, 4,792 European ancestry active individuals NA NR [2144171] (imputed) 6 systolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008404 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity (less vs more active half) interaction (1df) 3,495 European ancestry inactive individuals, 3,210 European ancestry active individuals NA NR [2144143] (imputed) 9 systolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008401 Genome-wide genotyping array 2019-08-12 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity (least vs most active quartile) interaction (1df) 1,913 European ancestry inactive individuals, 2,071 European ancestry active individuals NA NR [2144462] (imputed) 8 systolic blood pressure, physical activity http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003940 GCST008400 Genome-wide genotyping array 2019-08-08 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Systolic blood pressure x physical activity interaction (1df) 6,705 European ancestry individuals NA NR [2144171] (imputed) 9 systolic blood pressure, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0008002 GCST008392 Genome-wide genotyping array 2019-08-08 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. Diastolic blood pressure x physical activity interaction (1df) 6,704 European ancestry individuals NA NR [2144169] (imputed) 13 diastolic blood pressure, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0008002 GCST008389 Genome-wide genotyping array 2019-08-08 31167214 Osazuwa-Peters OL 2019-06-05 Hum Hered www.ncbi.nlm.nih.gov/pubmed/31167214 The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions. DIastolic blood pressure x physical activity interaction (2df) 6,704 European ancestry individuals NA NR [2144169] (imputed) 5 diastolic blood pressure, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0008002 GCST008390 Genome-wide genotyping array 2019-09-20 31417607 Gazal S 2019-07-30 Front Genet www.ncbi.nlm.nih.gov/pubmed/31417607 The Genetic Architecture of Chronic Mountain Sickness in Peru. Chronic mountain sickness 166 Quechua cases, 146 Quechua controls NA Affymetrix [1288199] 4 chronic mountain sickness http://www.ebi.ac.uk/efo/EFO_0010143 GCST008708 Genome-wide genotyping array 2017-06-08 28062665 Kawashima M 2017-01-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28062665 Genome-wide association studies identify PRKCB as a novel genetic susceptibility locus for primary biliary cholangitis in the Japanese population. Primary biliary cholangitis 1,381 Japanese ancestry cases, 1,505 Japanese ancestry controls 512 Japanese ancestry cases, 6,512 Japanese ancestry controls Affymetrix [425290] 9 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST004145 Genome-wide genotyping array 2017-01-25 27171184 Kuo HC 2016-05-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/27171184 Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease. Coronary artery aneurysm in Kawasaki disease 11 Taiwanese ancestry cases, 146 Taiwanese ancestry controls NA Affymetrix [559609] 20 coronary aneurysm http://www.ebi.ac.uk/efo/EFO_1000881 GCST003560 Genome-wide genotyping array 2017-05-11 28072414 Charney AW 2017-01-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/28072414 Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder. Bipolar disorder 13,903 European ancestry cases, 19,279 European ancestry controls. NA Affymetrix, Illumina [8837380] (imputed) 8 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST003962 Genome-wide genotyping array 2017-05-19 28067912 Lee JC 2017-01-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28067912 Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease. Poor prognosis in Crohn's disease 1,762 Northern European ancestry poor prognosis cases, 972 Northern European ancestry good prognosis controls. Affymetrix, Illumina [at least 7000000] (imputed) 4 disease prognosis measurement http://www.ebi.ac.uk/efo/EFO_0007936 GCST004053 Genome-wide genotyping array 2018-08-13 29892015 Roselli C 2018-06-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892015 Multi-ethnic genome-wide association study for atrial fibrillation. Atrial fibrillation 55,114 European ancestry cases, 482,295 European ancestry controls, 8,180 Japanese ancestry cases, 28,612 Japanese ancestry controls, 1,307 African American ancestry cases, 7,660 African American ancestry controls, 845 Hispanic cases, 4,177 Hispanic controls NA Affymetrix, Illumina [up to 12149979] (imputed) 228 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST006061 Genome-wide genotyping array 2019-02-21 30498476 Liu H 2018-11-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/30498476 Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins. Total cholesterol levels 139 Chinese ancestry dizygotic twin pairs NA Illumina [7405822] (imputed) 15 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST007203 Genome-wide genotyping array 2019-02-21 30498476 Liu H 2018-11-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/30498476 Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins. High density lipoprotein cholesterol levels 139 Chinese ancestry dizygotic twin pairs NA Illumina [7405822] (imputed) 20 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007202 Genome-wide genotyping array 2019-02-21 30498476 Liu H 2018-11-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/30498476 Heritability and Genome-Wide Association Study of Plasma Cholesterol in Chinese Adult Twins. Low density lipoprotein cholesterol levels 139 Chinese ancestry dizygotic twin pairs NA Illumina [7405822] (imputed) 12 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST007204 Genome-wide genotyping array 2018-12-17 25972531 Carter TC 2015-05-13 J Nutr www.ncbi.nlm.nih.gov/pubmed/25972531 Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults. Pyridoxal levels 2,158 Irish ancestry individuals NA NR [757337] 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST006797 Genome-wide genotyping array 2018-12-17 25972531 Carter TC 2015-05-13 J Nutr www.ncbi.nlm.nih.gov/pubmed/25972531 Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults. 4-pyridoxic acid levels 2,158 Irish ancestry individuals NA NR [757337] 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST006798 Genome-wide genotyping array 2018-12-17 25972531 Carter TC 2015-05-13 J Nutr www.ncbi.nlm.nih.gov/pubmed/25972531 Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults. Pyridoxal 5'-phosphate levels 2,158 Irish ancestry individuals NA NR [757337] 1 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST006799 Genome-wide genotyping array 2019-04-04 30452639 Butali A 2018-11-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30452639 Genomic analyses in african populations identify novel risk loci for cleft palate. Cleft lip with or without cleft palate 914 Sub-Saharan African ancestry cases, 2,159 Sub-Saharan African ancestry controls 401 Sub-Saharan African ancestry cases, 121 African American cases, 648 Sub-Saharan African ancestry controls, 186 African American controls Illumina [~ 17000000] (imputed) 0 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST007510 Genome-wide genotyping array 2019-04-04 30452639 Butali A 2018-11-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30452639 Genomic analyses in african populations identify novel risk loci for cleft palate. Cleft palate 205 Sub-Saharan African ancestry cases, 2,159 Sub-Saharan African ancestry controls 100 Sub-Saharan African ancestry cases, 79 African American cases, 648 Sub-Saharan African ancestry controls, 186 African American controls Illumina [~ 17000000] (imputed) 19 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST007509 Genome-wide genotyping array 2019-01-28 30610202 Ruderfer DM 2019-01-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30610202 Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide. Suicide attempts 2,433 British ancestry cases, 334,766 British ancestry controls NA Affymetrix [7797387] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST006978 Genome-wide genotyping array 2019-01-28 30610202 Ruderfer DM 2019-01-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30610202 Significant shared heritability underlies suicide attempt and clinically predicted probability of attempting suicide. Predicted suicide risk 24,546 European ancestry individuals NA Illumina [~ 9000000] (imputed) 2 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST006977 Genome-wide genotyping array 2019-02-21 30596066 Kong LL 2018-11-01 Ann Transl Med www.ncbi.nlm.nih.gov/pubmed/30596066 Genome-wide association study identifies RBFOX1 locus influencing brain glucose metabolism. Brain glucose metabolism (fluorodeoxyglucose uptake) 37 European ancestry Alzheimer's disease cases, 126 European ancestry individuals with mild cognitive impairment, 59 European ancestry controls NA Illumina [319792] 4 glucose metabolism measurement http://www.ebi.ac.uk/efo/EFO_0009367 GCST007206 Genome-wide genotyping array 2019-07-16 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Metabolic syndrome 1,211 Korean ancestry female cases, 639 Korean ancestry female controls 1,065 Korean ancestry female cases, 1,053 Korean ancestry female controls Affymetrix [NR] (imputed) 1 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST008140 Genome-wide genotyping array 2019-07-17 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Triglyceride levels 4,659 Korean ancestry females 5,273 Korean ancestry females Affymetrix [NR] (imputed) 9 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008150 Genome-wide genotyping array 2019-07-16 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. HDL cholesterol 4,659 Korean ancestry females 5,273 Korean ancestry females Affymetrix [NR] (imputed) 7 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008141 Genome-wide genotyping array 2019-07-16 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Systolic blood pressure 4,659 Korean ancestry females 5,273 Korean ancestry females Affymetrix [NR] (imputed) 5 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST008142 Genome-wide genotyping array 2019-07-16 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Diastolic blood pressure 4,659 Korean ancestry females 5,273 Korean ancestry females Affymetrix [NR] (imputed) 2 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST008143 Genome-wide genotyping array 2019-07-16 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Fasting plasma glucose 4,659 Korean ancestry females 5,273 Korean ancestry females Affymetrix [NR] (imputed) 7 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST008144 Genome-wide genotyping array 2019-07-16 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Waist circumference 4,659 Korean ancestry females 5,273 Korean ancestry females Affymetrix [NR] (imputed) 3 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST008145 Genome-wide genotyping array 2019-07-16 31170924 Kong S 2019-06-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/31170924 Identification of female-specific genetic variants for metabolic syndrome and its component traits to improve the prediction of metabolic syndrome in females. Metabolic syndrome up to 2,857 Korean ancestry male cases and male controls NA Affymetrix [NR] (imputed) 2 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST008146 Genome-wide genotyping array 2019-10-15 31527586 An J 2019-09-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31527586 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. Barrett's esophagus or Esophageal adenocarcinoma 8,998 European and unknown ancestry Barrett's esophagus cases, 4,680 European and unknown ancestry esophageal adenocarcinoma cases, 19,247 European and unknown ancestry controls NA Affymetrix [up to 7600000] (imputed) 3 esophageal adenocarcinoma, Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000478, http://www.ebi.ac.uk/efo/EFO_0000280 GCST008831 Genome-wide genotyping array 2019-10-15 31527586 An J 2019-09-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31527586 Gastroesophageal reflux GWAS identifies risk loci that also associate with subsequent severe esophageal diseases. Gastroesophageal reflux disease 80,265 European and unknown ancestry cases, 305,011 European and unknown ancestry controls NA Affymetrix, Illumina [up to 7600000] (imputed) 25 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST008832 Genome-wide genotyping array 2019-10-09 31513605 Jeon S 2019-09-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/31513605 Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes. Hypertension 8,842 Korean ancestry individuals NA NR [327872] 4 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST008828 Genome-wide genotyping array 2019-10-09 31513605 Jeon S 2019-09-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/31513605 Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes. Waist circumference 8,842 Korean ancestry individuals NA NR [327872] 7 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST008826 Genome-wide genotyping array 2019-10-09 31513605 Jeon S 2019-09-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/31513605 Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes. Type 2 diabetes 8,842 Korean ancestry individuals NA NR [327872] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST008827 Genome-wide genotyping array 2019-10-09 31513605 Jeon S 2019-09-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/31513605 Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes. Body mass index 8,842 Korean ancestry individuals NA NR [327872] 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008825 Genome-wide genotyping array 2019-10-09 31513605 Jeon S 2019-09-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/31513605 Structural equation modeling for hypertension and type 2 diabetes based on multiple SNPs and multiple phenotypes. Subscapular skin fold thickness 8,842 Korean ancestry individuals NA NR [327872] 5 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST008824 Genome-wide genotyping array 2019-03-15 30413934 Broce IJ 2018-11-09 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/30413934 Dissecting the genetic relationship between cardiovascular risk factors and Alzheimer's disease. Alzheimer's disease or cardiovascular risk factors (pleiotropy) 17,008 European ancestry Alzheimer's disease cases, 48,286 European ancestry type 2 diabetes cases, 17,283 European ancestry coronary artery disease cases, 425,739 European ancestry controls, 923,864 European ancestry individuals NA NR [up to 27375637] (imputed) 0 Alzheimer disease, total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, waist-hip ratio, body mass index, type 2 diabetes mellitus, high density lipoprotein cholesterol measurement, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004340, http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0001645 GCST007303 Genome-wide genotyping array 2019-02-28 27736895 Franceschini N 2016-10-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27736895 Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans. Diastolic blood pressure 19,706 Hispanic individuals, 18,744 African American individuals NA Illumina [up to 196725] 5 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST007238 Targeted genotyping array [MetaboChip] 2019-02-28 27736895 Franceschini N 2016-10-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27736895 Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans. Systolic blood pressure 19,706 Hispanic individuals, 18,744 African American individuals NA Illumina [up to 196725] 3 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST007237 Targeted genotyping array [MetaboChip] 2019-09-05 31413261 Deelen J 2019-08-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31413261 A meta-analysis of genome-wide association studies identifies multiple longevity genes. Longevity (age >90th survival percentile) 11,262 European ancestry cases, 25,483 European ancestry controls 2,557 European ancestry cases, 4,987 European ancestry controls Affymetrix, Illumina [up to 10786384] (imputed) 2 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST008598 Genome-wide genotyping array 2019-08-19 31271701 Thibord F 2019-07-04 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/31271701 A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process. Plasma factor V levels in venous thrombosis 510 European ancestry individuals 1,156 European ancestry individuals NR [6264382] (imputed) 2 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST008461 Genome-wide genotyping array 2019-08-19 31271701 Thibord F 2019-07-04 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/31271701 A Genome Wide Association Study on plasma FV levels identified PLXDC2 as a new modifier of the coagulation process. Plasma factor V levels in venous thrombosis (conditioned on rs6027) 510 European ancestry individuals 1,156 European ancestry individuals NR [6264382] (imputed) 11 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST008462 Genome-wide genotyping array 2022-09-21 31409809 Wang H 2019-08-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31409809 Genome-wide association analysis of self-reported daytime sleepiness identifies 42 loci that suggest biological subtypes. Daytime sleepiness 452,071 European ancestry individuals 34,452 European ancestry individuals Affymetrix [~ 96000000] (imputed) 0 excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0007875 GCST012956 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Superior frontal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 9 superior frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010329 GCST009219 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Superior parietal cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 superior parietal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010330 GCST009265 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Superior temporal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 13 superior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010331 GCST009213 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Supramarginal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 15 supramarginal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010332 GCST009205 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Frontal pole volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 frontal pole volume measurement http://www.ebi.ac.uk/efo/EFO_0010304 GCST009209 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Temporal pole volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 8 temporal pole volume measurement http://www.ebi.ac.uk/efo/EFO_0010334 GCST009195 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Transverse temporal cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 9 transverse temporal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010336 GCST009208 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Insular cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 15 insular cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010309 GCST009186 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Thalamus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 17 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST009264 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Caudate nucleus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0004830 GCST009257 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Putamen volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 putamen volume http://www.ebi.ac.uk/efo/EFO_0006932 GCST009262 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Pallidum volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 pallidum volume http://www.ebi.ac.uk/efo/EFO_0006933 GCST009261 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Hippocampal volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST009260 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Amygdala volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 10 amygdala volume http://www.ebi.ac.uk/efo/EFO_0006934 GCST009259 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Nucleus accumbens volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 8 nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006931 GCST009258 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Ventral diencephalon volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 4 ventral diencephalon volume measurement http://www.ebi.ac.uk/efo/EFO_0010337 GCST009194 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Choroid plexus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 choroid plexus volume measurement http://www.ebi.ac.uk/efo/EFO_0010293 GCST009211 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Lateral ventricle volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 18 lateral ventricle volume measurement http://www.ebi.ac.uk/efo/EFO_0008487 GCST009207 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Lateral ventricle temporal horn volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 49 temporal horn of lateral ventricle volume measurement http://www.ebi.ac.uk/efo/EFO_0010333 GCST009218 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Third ventricle volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 third ventricle volume measurement http://www.ebi.ac.uk/efo/EFO_0010335 GCST009214 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Fourth ventricle volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 15 fourth ventricle volume measurement http://www.ebi.ac.uk/efo/EFO_0010303 GCST009255 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Corpus callosum posterior volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 6 corpus callosum posterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010298 GCST009222 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Corpus callosum Mid-posterior volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 corpus collosum mid-posterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010300 GCST009217 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Corpus callosum central volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 10 corpus callosum central volume measurement http://www.ebi.ac.uk/efo/EFO_0010296 GCST009216 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Corpus callosum mid-anterior volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 5 corpus callosum mid-anterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010297 GCST009198 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Caudal anterior-cingulate cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 caudal anterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010289 GCST009175 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Caudal middle frontal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 caudal middle frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010290 GCST009178 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Cuneus cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 19 cuneus cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010301 GCST009181 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Entorhinal cortical volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 entorhinal cortical volume http://www.ebi.ac.uk/efo/EFO_0005092 GCST009177 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Fusiform gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 fusiform gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010305 GCST009176 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Inferior parietal cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 inferior parietal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010307 GCST009184 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Inferior temporal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 inferior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010308 GCST009185 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Isthmus-cingulate cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 18 isthmus cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010310 GCST009212 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Lateral occipital cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 lateral occipital cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010311 GCST009187 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Lateral orbital frontal cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 14 lateral orbital frontal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010312 GCST009189 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Lingual gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 14 lingual gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010314 GCST009188 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Medial orbital frontal cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 19 medial orbital frontal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010315 GCST009190 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Middle temporal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 middle temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010316 GCST009210 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Parahippocampal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 parahippocampal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010318 GCST009192 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Paracentral lobule volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 13 paracentral lobule volume measurement http://www.ebi.ac.uk/efo/EFO_0010317 GCST009191 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Pars opercularis volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 17 pars opercularis volume measurement http://www.ebi.ac.uk/efo/EFO_0010319 GCST009193 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Pars orbitalis volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 8 pars orbitalis volume measurement http://www.ebi.ac.uk/efo/EFO_0010320 GCST009180 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Pars triangularis volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 14 pars triangularis volume measurement http://www.ebi.ac.uk/efo/EFO_0010321 GCST009179 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Pericalcarine cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 10 pericalcarine cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010322 GCST009196 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Postcentral gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 postcentral gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010323 GCST009215 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Posterior-cingulate cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 posterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010324 GCST009183 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Precentral gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 7 precentral gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010325 GCST009199 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Precuneus cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 precuneus cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010326 GCST009182 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Rostral anterior cingulate cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 10 rostral anterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010327 GCST009221 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Rostral middle frontal gyrus volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 9 rostral middle frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010328 GCST009202 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Corpus callosum anterior volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 9 corpus callosum anterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010295 GCST009220 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 brain cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010287 GCST009197 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Cerebral white matter volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 white matter volume measurement http://www.ebi.ac.uk/efo/EFO_0008320 GCST009206 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Sub-cortical grey matter volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 14 grey matter volume measurement http://www.ebi.ac.uk/efo/EFO_0005420 GCST009201 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Total grey matter volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 12 grey matter volume measurement http://www.ebi.ac.uk/efo/EFO_0005420 GCST009263 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Whole brain grey matter density 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 21 Grey matter density measurement http://www.ebi.ac.uk/efo/EFO_0010306 GCST009200 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Total intracranial volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 18 intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0004886 GCST009204 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Cerebellum white matter volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 11 white matter volume measurement http://www.ebi.ac.uk/efo/EFO_0008320 GCST009254 Genome-wide genotyping array 2019-12-06 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Cerebellum cortex volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 17 cerebellar cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010291 GCST009203 Genome-wide genotyping array 2019-12-13 31530798 Alliey-Rodriguez N 2019-09-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31530798 NRXN1 is associated with enlargement of the temporal horns of the lateral ventricles in psychosis. Superior temporal sulcus banks volume 87 European ancestry Schizophrenia cases, 85 African American Schizophrenia cases, 15 Schizophrenia cases, 67 European ancestry Schizoaffective disorder cases, 53 African American Schizoaffective disorder cases, 7 Schizoaffective disorder cases, 130 European ancestry Bipolar disorders cases, 33 African American Bipolar disorders cases, 6 Bipolar disorders cases, 199 European ancestry controls, 79 African American controls, 16 controls NA Illumina [4322238] (imputed) 13 banks of the superior temporal sulcus volume measurement http://www.ebi.ac.uk/efo/EFO_0010286 GCST009256 Genome-wide genotyping array 2019-04-23 30431558 Smith SB 2018-11-13 Pain www.ncbi.nlm.nih.gov/pubmed/30431558 Genome-wide association reveals contribution of MRAS to painful temporomandibular disorder in males. Temporomandibular joint disorder 999 cases, 2,031 controls at least 2,232 European ancestry cases, at least 140,725 European ancestry controls, 2,597 Hispanic cases, 9,378 Hispanic controls, 710 cases, 1,122 controls Illumina [9700000] (imputed) 1 temporomandibular joint disorder http://www.ebi.ac.uk/efo/EFO_0005279 GCST007619 Genome-wide genotyping array 2018-12-10 29227965 Pilling LC 2017-12-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29227965 Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Parental longevity (combined parental attained age, Martingale residuals) 389,166 British ancestry individuals NA Affymetrix [11535925] (imputed) 38 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST006697 Genome-wide genotyping array 2018-12-10 29227965 Pilling LC 2017-12-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29227965 Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Parental longevity (both parents in top 10%) 7,182 cases, 79,767 controls NA Affymetrix [11535925] (imputed) 9 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST006698 Genome-wide genotyping array 2018-12-10 29227965 Pilling LC 2017-12-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29227965 Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Parental longevity (mother's age at death) 246,941 British ancestry individuals NA Affymetrix [11535925] (imputed) 3 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST006699 Genome-wide genotyping array 2018-12-10 29227965 Pilling LC 2017-12-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29227965 Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Parental longevity (mother's attained age) 412,937 British ancestry individuals NA Affymetrix [11535925] (imputed) 8 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST006696 Genome-wide genotyping array 2018-12-10 29227965 Pilling LC 2017-12-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29227965 Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Parental longevity (father's age at death) 317,652 British ancestry individuals NA Affymetrix [11535925] (imputed) 5 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST006700 Genome-wide genotyping array 2018-12-10 29227965 Pilling LC 2017-12-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29227965 Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Parental longevity (father's attained age) 415,311 British ancestry individuals NA Affymetrix [11535925] (imputed) 17 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST006701 Genome-wide genotyping array 2018-12-10 29227965 Pilling LC 2017-12-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/29227965 Human longevity: 25 genetic loci associated in 389,166 UK biobank participants. Parental longevity (combined parental age at death) 208,118 British ancestry individuals NA Affymetrix [11535925] (imputed) 8 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST006702 Genome-wide genotyping array 2019-03-13 30480742 Miki A 2018-11-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/30480742 Genome-Wide Association Study to Identify a New Susceptibility Locus for Central Serous Chorioretinopathy in the Japanese Population. Chronic central serous retinopathy 137 Japanese ancestry cases, 1,174 Japanese ancestry controls 183 Japanese ancestry cases, 2,071 Japanese ancestry controls Illumina [548653] 2 chronic central serous retinopathy http://www.ebi.ac.uk/efo/EFO_0009363 GCST007296 Genome-wide genotyping array 2019-04-29 30488612 Xiang B 2018-11-28 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/30488612 GWAS and network analysis of co-occurring nicotine and alcohol dependence identifies significantly associated alleles and network. Alcohol and nicotine co-dependence 1,079 European ancestry cases, 128 European ancestry controls, 1,303 African American cases, 791 African American controls 637 European ancestry cases, 41 European ancestry controls Illumina [37426733] (imputed) 0 alcohol and nicotine codependence http://www.ebi.ac.uk/efo/EFO_0004776 GCST007657 Genome-wide genotyping array 2019-05-07 30475886 Mekli K 2018-11-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/30475886 Frailty Index associates with GRIN2B in two representative samples from the United States and the United Kingdom. Frailty index 8,232 European ancestry individuals 5,248 European ancestry individuals Illumina [at least 1215858] 0 frailty measurement http://www.ebi.ac.uk/efo/EFO_0009885 GCST007716 Genome-wide genotyping array 2019-02-12 30412241 Takeuchi F 2018-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30412241 Genome-wide association study of cervical cancer suggests a role for ARRDC3 gene in human papillomavirus infection. Cervical cancer 2,609 East Asian ancestry cases, 4,712 East Asian ancestry controls 1,461 Han Chinese ancestry cases, 3,295 Han Chinese ancestry controls Affymetrix, Illumina [4602429] (imputed) 5 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST007119 Genome-wide genotyping array 2019-10-28 31591379 Sun Y 2019-10-07 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31591379 Genome-wide association study of alcohol dependence in male Han Chinese and cross-ethnic polygenic risk score comparison. Alcohol dependence 533 Han Chinese ancestry cases, 2,848 Han Chinese ancestry controls 146 Han Chinese ancestry cases, 200 Han Chinese ancestry controls Illumina [6449738] (imputed) 2 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST008966 Genome-wide genotyping array 2018-08-29 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) 12,758 European ancestry heavy drinkers, 1,326 African American or Afro-Caribbean heavy drinkers, 648 Asian ancestry heavy drinkers, 364 Hispanic or Latin American heavy drinkers, 43,947 European ancestry light drinkers, 8,239 African American or Afro-Caribbean light drinkers, 1,141 Asian ancestry light drinkers, 4,448 Hispanic or Latin American light drinkers 42,079 European ancestry heavy drinkers, 217 African American or Afro-Caribbean heavy drinkers, 282,294 Asian ancestry heavy drinkers, 124 Hispanic ancestry heavy drinkers, 74,757 European ancestry light drinkers, 845 African American light drinkers, 24,129 Asian ancestry light drinkers, 411 Hispanic light drinkers Affymetrix, Illumina [up to 39321347] (imputed) 41 diastolic blood pressure, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0007878 GCST006169 Genome-wide genotyping array 2018-10-18 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Systolic blood pressure x alcohol consumption interaction (2df test) 63,608 European ancestry drinkers, 10,193 African American or Afro-Caribbean heavy drinkers, 2,441 Asian ancestry drinkers, 5,084 Hispanic or Latin American drinkers, 27,494 European ancestry non-drinkers, 11,224 African American or Afro-Caribbean non-drinkers, 9,924 Asian ancestry non-drinkers, 3,387 Hispanic or Latin American non-drinkers 238,002 European ancestry drinkers, 2,280 African American drinkers, 54,081 Asian ancestry drinkers, 6,452 Hispanic drinkers, 43,316 European ancestry non-drinkers, 2,761 African American non-drinkers, 86,945 Asian ancestry non-drinkers, 6,925 Hispanic non-drinkers Affymetrix, Illumina [up to 39321347] (imputed) 114 systolic blood pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004329 GCST006434 Genome-wide genotyping array 2018-08-29 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Systolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) 12,758 European ancestry heavy drinkers, 1,326 African American or Afro-Caribbean heavy drinkers, 648 Asian ancestry heavy drinkers, 364 Hispanic or Latin American heavy drinkers, 43,947 European ancestry light drinkers, 8,239 African American or Afro-Caribbean light drinkers, 1,141 Asian ancestry light drinkers, 4,448 Hispanic or Latin American light drinkers 42,078 European ancestry heavy drinkers, 217 African American heavy drinkers, 282,294 Asian ancestry heavy drinkers, 124 Hispanic heavy drinkers, 74,706 European ancestry light drinkers, 845 African American light drinkers, 24,129 Asian ancestry light drinkers, 411 Hispanic light drinkers Affymetrix, Illumina [up to 39321347] (imputed) 43 systolic blood pressure, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0007878 GCST006170 Genome-wide genotyping array 2018-08-29 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Pulse pressure x alcohol consumption interaction (2df test) 91,099 European ancestry drinkers and non-drinkers, 21,416 African American or Afro-Caribbean drinkers and non-drinkers, 12,365 Asian ancestry drinkers and non-drinkers, 8,470 Hispanic or Latin American drinkers and non-drinkers 238,053 European ancestry drinkers, 2,280 African American drinkers, 54,080 Asian ancestry drinkers, 6,447 Hispanic ancestry drinkers, 43,318 European ancestry non-drinkers, 2,761 African American non-drinkers, 86,943 Asian ancestry non-drinkers, 6,923 Hispanic ancestry non-drinkers Affymetrix, Illumina [up to 39321347] (imputed) 59 pulse pressure measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0004329 GCST006168 Genome-wide genotyping array 2018-08-29 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Pulse pressure x alcohol consumption (light vs heavy) interaction (2df test) 56,705 European ancestry heavy and light drinkers, 9,725 African American or Afro-Caribbean heavy and light drinkers, 1,789 Asian ancestry heavy and light drinkers, 4,812 Hispanic or Latin American heavy and light drinkers 42,079 European ancestry heavy drinkers, 217 African American heavy drinkers, 282,294 Asian ancestry heavy drinkers, 124 Hispanic heavy drinkers, 74,756 European ancestry light drinkers, 845 African American light drinkers, 24,129 Asian ancestry light drinkers, 411 Hispanic light drinkers Affymetrix, Illumina [up to 39321347] (imputed) 17 pulse pressure measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0007878 GCST006171 Genome-wide genotyping array 2018-08-29 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Mean arterial pressure x alcohol consumption interaction (2df test) 91,110 European ancestry drinkers and non-drinkers, 21,416 African American or Afro-Caribbean drinkers and non-drinkers, 12,365 Asian ancestry drinkers and non-drinkers, 8,470 Hispanic or Latin American drinkers and non-drinkers 237,996 European ancestry drinkers, 2,280 African American drinkers, 54,080 Asian ancestry drinkers, 6,448 Hispanic drinkers, 43,315 European ancestry non-drinkers, 2,761 African ancestry non-drinkers, 86,943 Asian ancestry non-drinkers, 6,923 Hispanic non-drinkers Affymetrix, Illumina [up to 39321347] (imputed) 85 mean arterial pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0004329 GCST006167 Genome-wide genotyping array 2018-08-29 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Mean arterial pressure x alcohol consumption (light vs heavy) interaction (2df test) 56,705 European ancestry heavy and light drinkers, 9,725 African American or Afro-Caribbean heavy and light drinkers, 1,789 Asian ancestry heavy and light drinkers, 4,812 Hispanic or Latin American heavy and light drinkers 42,077 European ancestry heavy drinkers, 217 African American heavy drinkers, 282,294 Asian ancestry heavy drinkers, 124 Hispanic ancestry heavy drinkers, 74,701 European ancestry light drinkers, 845 African American light drinkers, 24,129 Asian ancestry light drinkers, 411 Hispanic light drinkers Affymetrix, Illumina [up to 39321347] (imputed) 41 mean arterial pressure, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0007878 GCST006172 Genome-wide genotyping array 2018-08-29 29912962 Feitosa MF 2018-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/29912962 Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries. Diastolic blood pressure x alcohol consumption interaction (2df test) 63,607 European ancestry drinkers, 10,193 African American or Afro-Caribbean drinkers, 2,441 Asian ancestry drinkers, 5,084 Hispanic or Latin American drinkers, 27,492 European ancestry non-drinkers, 11,223 African American or Afro-Caribbean non-drinkers, 9,924 Asian ancestry non-drinkers, 3,387 Hispanic or Latin American non-drinkers 238,058 European ancestry drinkers, 2,280 African American drinkers, 54,081 Asian ancestry drinkers, 6,448 Hispanic drinkers, 43,318 European ancestry non-drinkers, 2,761 African American non-drinkers, 86,943 Asian ancestry non-drinkers, 6,923 Hispanic non-drinkers Affymetrix, Illumina [up to 39321347] (imputed) 114 diastolic blood pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004329 GCST006166 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal AB1-42 levels in Alzheimer's disease dementia 190 European ancestry AD dementia cases NA Illumina [8344766] (imputed) 3 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST006990 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid t-tau levels in Alzheimer's disease dementia 190 European ancestry cases NA Illumina [8340470] (imputed) 3 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST006991 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid p-tau levels in Alzheimer's disease dementia 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8344766] (imputed) 4 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST006992 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Hippocampal volume in Alzheimer's disease dementia 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8437147] (imputed) 15 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST006993 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (immediate recall) in Alzheimer's disease dementia 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8411492] (imputed) 4 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST006994 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (delayed recall) in Alzheimer's disease dementia 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8411492] (imputed) 2 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST006995 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal AB1-42 levels in mild cognitive impairment 581 European ancestry MCI dementia cases NA Illumina [8448490] (imputed) 4 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST006996 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid t-tau levels in mild cognitive impairment 581 European ancestry cases NA Illumina [8449920] (imputed) 3 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST006997 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid p-tau levels in mild cognitive impairment 581 European ancestry mild cognitive impairment cases NA Illumina [8446615] (imputed) 7 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST006998 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Hippocampal volume in mild cognitive impairment 581 European ancestry mild cognitive impairment cases NA Illumina [7938386] (imputed) 6 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST007013 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (immediate recall) in mild cognitive impairment 581 European ancestry mild cognitive impairment cases NA Illumina [7992243] (imputed) 5 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST006999 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (delayed recall) in mild cognitive impairment 581 European ancestry mild cognitive impairment cases NA Illumina [7992243] (imputed) 5 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST007000 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal AB1-42 levels in normal cognition 305 European ancestry cognitively normal individuals NA Illumina [8257341] (imputed) 16 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST007001 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid t-tau levels in normal cognition 305 European ancestry cognitively normal individuals NA Illumina [8248960] (imputed) 7 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST007002 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid p-tau levels in normal cognition 305 European ancestry cognitively normal individuals NA Illumina [8252679] (imputed) 3 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST007003 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Hippocampal volume in normal cognition 305 European ancestry cognitively normal individuals NA Illumina [7770817] (imputed) 2 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST007004 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (immediate recall) in normal cognition 305 European ancestry cognitively normal individuals NA Illumina [7797526] (imputed) 9 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST007005 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (delayed recall) in normal cognition 305 European ancestry cognitively normal individuals NA Illumina [7797256] (imputed) 17 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST007006 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid AB1-42 levels 305 European ancestry cognitively normal individuals, 581 European ancestry mild cognitive impairment cases, 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8454933] (imputed) 6 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST007012 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid t-tau levels 305 European ancestry cognitively normal individuals, 581 European ancestry mild cognitive impairment cases, 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8454470] (imputed) 4 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST007007 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Cerebrospinal fluid p-tau levels 305 European ancestry cognitively normal individuals, 581 European ancestry mild cognitive impairment cases, 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8454806] (imputed) 6 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST007008 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Hippocampal volume 305 European ancestry cognitively normal individuals, 581 European ancestry mild cognitive impairment cases, 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8056701] (imputed) 8 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST007009 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (immediate recall) 305 European ancestry cognitively normal individuals, 581 European ancestry mild cognitive impairment cases, 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8066948] (imputed) 4 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST007011 Genome-wide genotyping array 2019-01-31 29274321 Chung J 2017-12-20 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/29274321 Genome-wide association study of Alzheimer's disease endophenotypes at prediagnosis stages. Logical memory (delayed recall) 305 European ancestry cognitively normal individuals, 581 European ancestry mild cognitive impairment cases, 190 European ancestry Alzheimer's disease dementia cases NA Illumina [8066948] (imputed) 4 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST007010 Genome-wide genotyping array 2018-08-14 29924316 Byun J 2018-06-19 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/29924316 Genome-Wide Association Study of Familial Lung Cancer. Familial lung cancer 1,993 European ancestry cases, 33,960 European ancestry controls NA Illumina [9327222] (imputed) 20 lung carcinoma, family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0006953 GCST006086 Genome-wide genotyping array 2018-08-14 29924316 Byun J 2018-06-19 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/29924316 Genome-Wide Association Study of Familial Lung Cancer. Familial lung adenocarcinoma 775 European ancestry cases, 31,563 European ancestry controls NA Illumina [8672852] (imputed) 36 lung adenocarcinoma, family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0000571, http://www.ebi.ac.uk/efo/EFO_0006953 GCST006087 Genome-wide genotyping array 2018-08-14 29924316 Byun J 2018-06-19 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/29924316 Genome-Wide Association Study of Familial Lung Cancer. Familial squamous cell lung carcinoma 367 European ancestry cases, 31,563 European ancestry controls NA Illumina [7959153] (imputed) 68 squamous cell lung carcinoma, family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0000708, http://www.ebi.ac.uk/efo/EFO_0006953 GCST006088 Genome-wide genotyping array 2019-03-26 30378284 Smajlagic D 2018-10-31 Brain Behav www.ncbi.nlm.nih.gov/pubmed/30378284 Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC. Verbal intelligence quotient (cesarean section interaction) 519 European ancestry child cases, 1,902 European ancestry child controls NA Illumina [2141747] (imputed) 4 cesarean section, intelligence http://www.ebi.ac.uk/efo/EFO_0009636, http://www.ebi.ac.uk/efo/EFO_0004337 GCST007403 Genome-wide genotyping array 2019-03-26 30378284 Smajlagic D 2018-10-31 Brain Behav www.ncbi.nlm.nih.gov/pubmed/30378284 Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC. Performance intelligence quotient (cesarean section interaction) 519 European ancestry child cases, 1,902 European ancestry child controls NA Illumina [2141747] (imputed) 2 cesarean section, intelligence http://www.ebi.ac.uk/efo/EFO_0009636, http://www.ebi.ac.uk/efo/EFO_0004337 GCST007404 Genome-wide genotyping array 2019-03-26 30378284 Smajlagic D 2018-10-31 Brain Behav www.ncbi.nlm.nih.gov/pubmed/30378284 Moderating effect of mode of delivery on the genetics of intelligence: Explorative genome-wide analyses in ALSPAC. Full scale intelligence quotient (cesarean section interaction) 519 European ancestry child cases, 1,902 European ancestry child controls NA Illumina [2141747] (imputed) 4 cesarean section, intelligence http://www.ebi.ac.uk/efo/EFO_0009636, http://www.ebi.ac.uk/efo/EFO_0004337 GCST007405 Genome-wide genotyping array 2020-04-17 30482948 Walters RK 2018-11-26 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/30482948 Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders. Alcohol dependence 11,569 European ancestry cases, 34,999 European ancestry controls, 3,335 African American cases, 2,945 African American controls 1,232 European ancestry cases, 22,614 European ancestry controls, 1,791 African American cases, 2,413 African American controls Illumina [at least 4006464] (imputed) 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST009886 Genome-wide genotyping array 2019-04-09 30450575 Hojfeldt SG 2018-11-18 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/30450575 Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008. PEG-asparaginase hypersensitivity without enzyme activity in childhood acute lymphoblastic leukaemia 59 European ancestry cases, 772 European ancestry controls NA Illumina [NR] 11 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST007540 Genome-wide genotyping array 2019-04-09 30450575 Hojfeldt SG 2018-11-18 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/30450575 Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008. Silent asparaginase inactivation in childhood acute lymphoblastic leukaemia 32 European ancestry cases, 772 European ancestry controls NA Illumina [NR] 0 asparaginase activity measurement http://www.ebi.ac.uk/efo/EFO_0009790 GCST007539 Genome-wide genotyping array 2019-04-09 30450575 Hojfeldt SG 2018-11-18 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/30450575 Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008. PEG-asparaginase hypersensitivity in childhood acute lymphoblastic leukaemia (allergic reaction grade 2 or more) 106 European ancestry cases, 772 European ancestry controls NA Illumina [NR] 0 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST007541 Genome-wide genotyping array 2019-01-15 30395268 Khanshour AM 2018-11-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30395268 Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci. Adolescent idiopathic scoliosis 2,295 East Asian ancestry cases, 11,084 East Asian ancestry controls, 1,503 European ancestry cases, 18,594 European ancestry controls 2,737 East Asian ancestry cases, 56,815 East Asian ancestry controls, 1,421 European ancestry cases, 1,966 European ancestry controls Affymetrix, Illumina [3493832] (imputed) 10 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST006902 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer's disease 4,120 Spanish ancestry cases, 11,999 cases, 3,289 Spanish ancestry controls, 9,236 controls 1,943 Spanish ancestry cases, 3,016 Spanish ancestry controls Affymetrix [up to 7700000] (imputed) 6 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009019 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer's disease 4,120 Spanish ancestry cases, 17,008 cases, 3,289 Spanish ancestry controls, 37,154 controls 1,943 Spanish ancestry cases, 8,572 cases, 3,016 Spanish ancestry controls, 11,312 controls Affymetrix [up to 7055881] (imputed) 20 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009021 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer's disease 4,120 European ancestry cases, 3,289 European ancestry controls NA Affymetrix [7700000] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009020 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer’s disease and/or vascular dementia (clinical subgroup VaD+) 1,168 Spanish ancestry cases, 3,289 Spanish ancestry controls NA Affymetrix [~ 7700000] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009025 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer’s disease (clinical subgroup AD+) 3,797 Spanish ancestry cases, 3,289 Spanish ancestry controls NA Affymetrix [~ 7700000] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009022 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer’s disease (clinical subgroup AD++) 2,611 Spanish ancestry cases, 3,289 Spanish ancestry controls NA Affymetrix [~ 7700000] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009023 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer’s disease (clinical subgroup AD+++) 1,854 Spanish ancestry cases, 3,289 Spanish ancestry controls NA Affymetrix [~ 7700000] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009024 Genome-wide genotyping array 2019-11-13 31473137 Moreno-Grau S 2019-08-13 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/31473137 Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Alzheimer’s disease and/or vascular dementia (clinical subgroup VaD++) 373 Spanish ancestry cases, 3,289 Spanish ancestry controls NA Affymetrix [~ 7700000] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST009026 Genome-wide genotyping array 2019-07-05 30230522 Zhang S 2018-09-19 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/30230522 Subtype-Specific Inherited Predisposition to Pemphigus in Chinese Population. Pemphigus foliaceus 72 Chinese ancestry cases, 501 Chinese ancestry controls 32 Chinese ancestry cases, 604 Chinese ancestry controls Affymetrix [416397] 0 pemphigus foliaceus http://www.ebi.ac.uk/efo/EFO_0008601 GCST008067 Genome-wide genotyping array 2019-07-05 30230522 Zhang S 2018-09-19 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/30230522 Subtype-Specific Inherited Predisposition to Pemphigus in Chinese Population. Pemphigus 350 Chinese ancestry cases, 501 Chinese ancestry controls 146 Chinese ancestry cases, 604 Chinese ancestry controls Affymetrix [416397] 2 pemphigus http://www.ebi.ac.uk/efo/EFO_1000749 GCST008069 Genome-wide genotyping array 2019-07-05 30230522 Zhang S 2018-09-19 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/30230522 Subtype-Specific Inherited Predisposition to Pemphigus in Chinese Population. Pemphigus vulgaris 255 Chinese ancestry cases, 501 Chinese ancestry controls 110 Chinese ancestry cases, 604 Chinese ancestry controls Affymetrix [416397] 2 pemphigus vulgaris http://www.ebi.ac.uk/efo/EFO_0004719 GCST008068 Genome-wide genotyping array 2019-09-02 31263887 Adams MJ 2019-07-01 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/31263887 Factors associated with sharing e-mail information and mental health survey participation in large population cohorts. Mental health study participation (provided email address) 224,321 British ancestry cases, 147,096 British ancestry controls NA NR [16367095] (imputed) 16 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST008549 Genome-wide genotyping array 2019-09-02 31263887 Adams MJ 2019-07-01 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/31263887 Factors associated with sharing e-mail information and mental health survey participation in large population cohorts. Mental health study participation (completed survey) 122,647 British ancestry cases, 248,781 British ancestry controls NA NR [16367095] (imputed) 40 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST008550 Genome-wide genotyping array 2019-07-24 31277774 Lipunova N 2018-09-15 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/31277774 Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer. Non-muscle-invasive bladder cancer age at diagnosis 653 European ancestry cases 1470 European ancestry cases Illumina [11914228] (imputed) 0 age at diagnosis, urinary bladder carcinoma http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0004986 GCST008217 Genome-wide genotyping array 2019-07-24 31277774 Lipunova N 2018-09-15 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/31277774 Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer. Non-muscle-invasive bladder cancer age at diagnosis (< 70 years vs ≥ 70 years) 298 European ancestry cases under 70 years, 355 European ancestry cases 70 years or older 329 European ancestry cases under 70 years, 1,141 European ancestry cases 70 years or older Illumina [11914228] (imputed) 0 age at diagnosis, urinary bladder carcinoma http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0004986 GCST008218 Genome-wide genotyping array 2019-07-24 31277774 Lipunova N 2018-09-15 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/31277774 Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer. Non-muscle-invasive bladder cancer tumour size 633 European ancestry cases 302 European ancestry cases Illumina [11914228] (imputed) 1 urinary bladder carcinoma, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0004986, http://www.ebi.ac.uk/efo/EFO_0008336 GCST008216 Genome-wide genotyping array 2019-07-24 31277774 Lipunova N 2018-09-15 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/31277774 Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer. Non-muscle-invasive bladder cancer tumour size (< 3 cm vs ≥ 3 cm) 633 European ancestry cases 302 European ancestry cases Illumina [11914228] (imputed) 0 urinary bladder carcinoma, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0004986, http://www.ebi.ac.uk/efo/EFO_0008336 GCST008219 Genome-wide genotyping array 2019-07-24 31277774 Lipunova N 2018-09-15 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/31277774 Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer. Non-muscle-invasive bladder cancer tumour stage (Tis/T1 vs Ta) 209 European ancestry stage Tis/T1 cases, 444 European ancestry stage Ta cases 414 European ancestry stage Tis/T1 cases, 1,056 European ancestry stage Ta cases Illumina [11914228] (imputed) 0 urinary bladder carcinoma, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0004986, http://www.ebi.ac.uk/efo/EFO_0008336 GCST008220 Genome-wide genotyping array 2019-07-24 31277774 Lipunova N 2018-09-15 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/31277774 Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer. Non-muscle-invasive bladder cancer tumour grade (G3 vs G2/G1) 207 European ancestry grade G3 cases, 436 European ancestry grade G2/G1 cases 304 European ancestry grade G3 cases, 1,019 European ancestry grade G2/G1 cases Illumina [11914228] (imputed) 0 urinary bladder carcinoma, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0004986, http://www.ebi.ac.uk/efo/EFO_0008336 GCST008221 Genome-wide genotyping array 2019-07-24 31277774 Lipunova N 2018-09-15 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/31277774 Genome-wide Association Study for Tumour Stage, Grade, Size, and Age at Diagnosis of Non-muscle-invasive Bladder Cancer. Non-muscle-invasive bladder cancer EORTC risk category 311 European ancestry high risk cases, 342 European ancestry low/intermediate risk cases NA Illumina [11914228] (imputed) 0 urinary bladder carcinoma, disease prognosis measurement http://purl.obolibrary.org/obo/MONDO_0004986, http://www.ebi.ac.uk/efo/EFO_0007936 GCST008222 Genome-wide genotyping array 2019-09-05 31413261 Deelen J 2019-08-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31413261 A meta-analysis of genome-wide association studies identifies multiple longevity genes. Longevity (age >99th survival percentile) 3,484 European ancestry cases, 2,178 East Asian ancestry cases, 25,483 European ancestry controls, 2,299 East Asian ancestry controls NA Illumina [up to 9449311] (imputed) 7 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST008601 Genome-wide genotyping array 2019-09-05 31413261 Deelen J 2019-08-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31413261 A meta-analysis of genome-wide association studies identifies multiple longevity genes. Longevity (age >90th survival percentile) 11,262 European ancestry cases, 2,178 East Asian ancestry cases, 177 African American cases, 25,483 European ancestry controls, 2,299 East Asian ancestry controls, 211 African American controls. NA Affymetrix, Illumina [up to 10786384] (imputed) 8 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST008600 Genome-wide genotyping array 2019-09-05 31413261 Deelen J 2019-08-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31413261 A meta-analysis of genome-wide association studies identifies multiple longevity genes. Longevity (age >99th survival percentile) 3,484 European ancestry cases, 25,483 European ancestry controls 1,911 European ancestry cases, 4,987 European ancestry controls Illumina [up to 9449311] (imputed) 2 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST008599 Genome-wide genotyping array 2017-06-02 28060188 Hamet P 2017-01-16 J Hypertens www.ncbi.nlm.nih.gov/pubmed/28060188 PROX1 gene CC genotype as a major determinant of early onset of type 2 diabetes in slavic study participants from Action in Diabetes and Vascular Disease: Preterax and Diamicron MR Controlled Evaluation study. Type 2 diabetes (age of onset) 2,307 Celtic ancestry individuals, 1,102 Slavic ancestry individuals NA Affymetrix [5045527] (imputed) 26 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST004125 Genome-wide genotyping array 2017-02-15 28090565 Tsai EA 2016-05-26 Cell Mol Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/28090565 THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome. Liver disease severity in Alagille syndrome 97 European ancestry mild cases, 64 European ancestry severe cases NA Illumina [579677] 2 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST003616 Genome-wide genotyping array 2017-05-16 28061514 Nannini DR 2017-01-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/28061514 A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population. Optic nerve measurement (cup-to-disc ratio) 3,596 Latino individuals 941 Latino individuals Illumina [6844888] (imputed) 4 cup-to-disc ratio measurement http://www.ebi.ac.uk/efo/EFO_0006939 GCST004047 Genome-wide genotyping array 2017-05-11 28051079 Warner SC 2017-01-04 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28051079 Genome-wide association scan of neuropathic pain symptoms post total joint replacement highlights a variant in the protein-kinase C gene. Possible neuropathic pain in post total joint replacement surgery for osteoarthritis 109 cases, 504 controls. NA Illumina [548381] 4 neuropathic pain http://www.ebi.ac.uk/efo/EFO_0005762 GCST003963 Genome-wide genotyping array 2018-12-11 30223776 Hwang LD 2018-09-17 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/30223776 Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste. Bitter taste perception (multivariate analysis) 1,999 European ancestry individuals from 929 twin families NA Illumina [4381914] (imputed) 11 sensory perception of bitter taste http://purl.obolibrary.org/obo/GO_0050913 GCST006703 Genome-wide genotyping array 2018-12-11 30223776 Hwang LD 2018-09-17 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/30223776 Bivariate genome-wide association analysis strengthens the role of bitter receptor clusters on chromosomes 7 and 12 in human bitter taste. Bitter taste perception 1,999 European ancestry individuals from 929 twin families NA Illumina [4381914] (imputed) 6 sensory perception of bitter taste http://purl.obolibrary.org/obo/GO_0050913 GCST006704 Genome-wide genotyping array 2019-07-12 31164008 Mullins N 2019-06-05 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31164008 GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Suicide attempts in major depressive disorder 1,622 European ancestry attempters, 8,786 European ancestry nonattempters NA NR [8482392] (imputed) 20 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST008118 Genome-wide genotyping array 2019-07-12 31164008 Mullins N 2019-06-05 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31164008 GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Suicide attempts in major depressive disorder or bipolar disorder or schizophrenia 1,622 European ancestry attempters with major depressive disorder, 8,786 European ancestry nonattempters with major depressive disorder, 3,264 European ancestry attempters with bipolar disorder, 5,500 European ancestry nonattempters with bipolar disorder, 1,683 European ancestry attempters with schizophrenia, 2,946 European ancestry nonattempters with schizophrenia NA NR [at least 8482392] (imputed) 40 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST008123 Genome-wide genotyping array 2019-07-12 31164008 Mullins N 2019-06-05 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31164008 GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Suicide attempts in bipolar disorder 3,264 European ancestry attempters, 5,500 European ancestry nonattempters NA NR [8807005] (imputed) 14 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST008119 Genome-wide genotyping array 2019-07-12 31164008 Mullins N 2019-06-05 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31164008 GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Suicide attempts in schizophrenia 1,683 European ancestry attempters, 2,946 European ancestry nonattempters NA NR [8814543] (imputed) 20 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST008120 Genome-wide genotyping array 2019-07-12 31164008 Mullins N 2019-06-05 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31164008 GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Suicide attempts in major depressive disorder or bipolar disorder 1,622 European ancestry attempters with major depressive disorder, 8,786 European ancestry nonattempters with major depressive disorder, 3,264 European ancestry attempters with bipolar disorder, 5,500 European ancestry nonattempters with bipolar disorder 7,092 European ancestry attempters with major depressive disorder or bipolar disorder, 51,761 European ancestry nonattempters with major depressive disorder or bipolar disorder NR [at least 8482392] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST008121 Genome-wide genotyping array 2019-07-12 31164008 Mullins N 2019-06-05 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31164008 GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores. Suicide attempts in bipolar disorder or schizophrenia 3,264 European ancestry attempters with bipolar disorder, 5,500 European ancestry nonattempters with bipolar disorder, 1,683 European ancestry attempters with schizophrenia, 2,946 European ancestry nonattempters with schizophrenia NA NR [at least 8807005] (imputed) 18 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST008122 Genome-wide genotyping array 2018-12-17 28957414 Pilling LC 2017-09-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/28957414 Red blood cell distribution width: Genetic evidence for aging pathways in 116,666 volunteers. Red cell distribution width 116,666 British ancestry individuals NA Affymetrix [16832071] (imputed) 195 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST006804 Genome-wide genotyping array 2019-03-13 30487263 Pollack S 2018-11-28 Diabetes www.ncbi.nlm.nih.gov/pubmed/30487263 Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetic retinopathy (all NPDR and PDR) 1,079 European ancestry cases, 1,970 European ancestry controls, 911 African American cases, 941 African American controls 7,178 East Asian ancestry cases, 6,525 East Asian ancestry controls, 214 South East Asian ancestry cases, 557 South East Asian ancestry controls, 315 South Asian ancestry cases, 669 South Asian ancestry controls, 8,205 European ancestry cases, 7,713 European ancestry controls, 1,470 Hispanic cases, 1,240 Hispanic controls Affymetrix, Illumina [NR] (imputed) 19 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST007292 Genome-wide genotyping array 2019-03-13 30487263 Pollack S 2018-11-28 Diabetes www.ncbi.nlm.nih.gov/pubmed/30487263 Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Proliferative diabetic retinopathy (vs NPDR and no DR) 398 European ancestry cases, 2,848 European ancestry controls, 1,097 African American cases, 1,514 African American controls 918 East Asian ancestry cases, 1,167 East Asian ancestry controls, 2,038 European ancestry cases, 6,783 European ancestry controls, 232 Hispanic cases, 2,194 Hispanic controls Affymetrix, Illumina [NR] (imputed) 19 proliferative diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0009322 GCST007289 Genome-wide genotyping array 2019-03-13 30487263 Pollack S 2018-11-28 Diabetes www.ncbi.nlm.nih.gov/pubmed/30487263 Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Diabetic retinopathy (moderate NPDR and PDR) 644 European ancestry cases, 1,970 European ancestry controls, 768 African American cases, 941 African American controls 2,388 East Asian ancestry cases, 6,219 East Asian ancestry controls, 1,658 European ancestry cases, 3,019 European ancestry controls, 1,014 Hispanic cases, 1,240 Hispanic controls Affymetrix, Illumina [NR] (imputed) 20 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST007290 Genome-wide genotyping array 2019-03-13 30487263 Pollack S 2018-11-28 Diabetes www.ncbi.nlm.nih.gov/pubmed/30487263 Multiethnic Genome-wide Association Study of Diabetic Retinopathy using Liability Threshold Modeling of Duration of Diabetes and Glycemic Control. Proliferative diabetic retinopathy (vs no DR) 398 European ancestry cases, 1,970 European ancestry controls, 1,097 African American cases, 941 African American controls 1,354 East Asian ancestry cases, 1130 East Asian ancestry controls, 801 European ancestry cases, 2,880 European ancestry controls, 232 Hispanic cases, 1,048 Hispanic controls Affymetrix, Illumina [NR] (imputed) 19 proliferative diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0009322 GCST007291 Genome-wide genotyping array 2018-12-17 26961502 Wood AR 2016-03-10 Diabetologia www.ncbi.nlm.nih.gov/pubmed/26961502 Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively. Body mass index 29,925 British ancestry cases, 89,763 British ancestry controls NA NR [9288881] (imputed) 36 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST006802 Genome-wide genotyping array 2018-12-17 26961502 Wood AR 2016-03-10 Diabetologia www.ncbi.nlm.nih.gov/pubmed/26961502 Variants in the FTO and CDKAL1 loci have recessive effects on risk of obesity and type 2 diabetes, respectively. Type 2 diabetes 4,040 British ancestry cases, 113,735 British ancestry controls NA NR [9288881] (imputed) 13 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST006801 Genome-wide genotyping array 2018-08-21 29917119 Schmit SL 2018-06-16 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/29917119 Novel Common Genetic Susceptibility Loci for Colorectal Cancer. Colorectal cancer 36,948 European ancestry cases, 30,864 European ancestry controls 12,952 European ancestry cases, 48,383 European ancestry controls, 8,580 East Asian ancestry cases, 13,050 East Asian ancestry controls, 1,611 Hispanic cases, 4,330 Hispanic controls, 1,894 African American cases, 4,703 African American controls Affymetrix, Illumina [12931465] (imputed) 28 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST006131 Genome-wide genotyping array 2019-02-11 30674883 Jin Y 2019-01-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30674883 Early-onset autoimmune vitiligo associated with an enhancer variant haplotype that upregulates class II HLA expression. Vitiligo (late onset) 1,467 European ancestry cases, 19,156 European ancestry controls 977 European ancestry cases, 727 European ancestry controls NR [up to 494043] (imputed) 1 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST007112 Genome-wide genotyping array 2019-02-11 30674883 Jin Y 2019-01-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30674883 Early-onset autoimmune vitiligo associated with an enhancer variant haplotype that upregulates class II HLA expression. Vitiligo (early onset) 704 European ancestry cases, 9,031 European ancestry controls 375 European ancestry cases, 1,455 European ancestry controls NR [up to 494043] (imputed) 2 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST007111 Genome-wide genotyping array 2019-09-02 31155012 Nakahara S 2019-06-03 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31155012 Dentate gyrus volume deficit in schizophrenia. Dentate gyrus volume x schizophrenia interaction 88 European ancestry cases, 22 Black or African American cases, 18 Asian ancestry cases, 1 American Indian or Alaskan Native ancestry case, 1 Native Hawaiian or Pacific Islander ancestry case, 111 European ancestry controls, 18 Black or African American controls, 13 Asian ancestry controls, 2 American Indian or Alaskan Native ancestry controls, 1 Native Hawaiian or Pacific Islander ancestry control NA Illumina [12049533] (imputed) 1 dentate gyrus volume measurement, schizophrenia http://www.ebi.ac.uk/efo/EFO_0010083, http://purl.obolibrary.org/obo/MONDO_0005090 GCST008557 Genome-wide genotyping array 2019-09-02 31155012 Nakahara S 2019-06-03 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31155012 Dentate gyrus volume deficit in schizophrenia. Dentate gyrus volume 199 European ancestry individuals, 40 Black or African American individuals, 31 Asian ancestry individuals, 3 American Indian or Alaskan Native ancestry individuals, 2 Native Hawaiian or Pacific Islander ancestry individuals NA Illumina [12049533] (imputed) 0 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST008558 Genome-wide genotyping array 2020-01-09 31554410 Aung N 2019-09-25 Circulation www.ncbi.nlm.nih.gov/pubmed/31554410 Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated with Cardiac Morphogenesis and Heart Failure Development. Left ventricular end-diastolic volume 16,920 European ancestry individuals 1,742 European ancestry individuals, 1,083 African American individuals, 586 Chinese ancestry individuals, 972 Hispanic individuals Affymetrix [~ 7000000] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST009397 Genome-wide genotyping array 2020-01-09 31554410 Aung N 2019-09-25 Circulation www.ncbi.nlm.nih.gov/pubmed/31554410 Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated with Cardiac Morphogenesis and Heart Failure Development. Left ventricular mass 16,920 European ancestry individuals 1,742 European ancestry individuals, 1,083 African American individuals, 586 Chinese ancestry individuals, 972 Hispanic individuals Affymetrix [~ 7000000] (imputed) 0 left ventricular mass http://www.ebi.ac.uk/efo/EFO_0009289 GCST009396 Genome-wide genotyping array 2020-01-09 31554410 Aung N 2019-09-25 Circulation www.ncbi.nlm.nih.gov/pubmed/31554410 Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated with Cardiac Morphogenesis and Heart Failure Development. Left ventricular end-systolic volume 16,920 European ancestry individuals 1,742 European ancestry individuals, 1,083 African American individuals, 586 Chinese ancestry individuals, 972 Hispanic individuals Affymetrix [~ 7000000] (imputed) 0 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST009394 Genome-wide genotyping array 2020-01-09 31554410 Aung N 2019-09-25 Circulation www.ncbi.nlm.nih.gov/pubmed/31554410 Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated with Cardiac Morphogenesis and Heart Failure Development. Left ventricular stroke volume 16,917 European ancestry individuals 1,742 European ancestry individuals, 1,083 African American individuals, 586 Chinese ancestry individuals, 972 Hispanic individuals Affymetrix [~ 7000000] (imputed) 0 left ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0010555 GCST009392 Genome-wide genotyping array 2020-01-09 31554410 Aung N 2019-09-25 Circulation www.ncbi.nlm.nih.gov/pubmed/31554410 Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated with Cardiac Morphogenesis and Heart Failure Development. Left ventricular ejection fraction 16,923 European ancestry individuals 1,742 European ancestry individuals, 1,083 African American individuals, 586 Chinese ancestry individuals, 972 Hispanic individuals Affymetrix [~ 7000000] (imputed) 1 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST009395 Genome-wide genotyping array 2020-01-09 31554410 Aung N 2019-09-25 Circulation www.ncbi.nlm.nih.gov/pubmed/31554410 Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated with Cardiac Morphogenesis and Heart Failure Development. Left ventricular mass to end-diastolic volume ratio 16,884 European ancestry individuals 1,742 European ancestry individuals, 1,083 African American individuals, 586 Chinese ancestry individuals, 972 Hispanic individuals Affymetrix [~ 7000000] (imputed) 0 Left ventricular mass to end-diastolic volume ratio http://www.ebi.ac.uk/efo/EFO_0010556 GCST009393 Genome-wide genotyping array 2019-12-16 31557306 Wang RS 2019-09-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31557306 Pharmacogenomics and Placebo Response in a Randomized Clinical Trial in Asthma. Subjective response to placebo treatment in childhood asthma (change in cough/wheeze) 250 European ancestry children NA Illumina [NR] (imputed) 11 respiratory symptom change measurement, response to placebo http://www.ebi.ac.uk/efo/EFO_0010068, http://www.ebi.ac.uk/efo/EFO_0008344 GCST009277 Genome-wide genotyping array 2019-12-16 31557306 Wang RS 2019-09-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31557306 Pharmacogenomics and Placebo Response in a Randomized Clinical Trial in Asthma. Response to placebo treatment in childhood asthma (FVC change) 250 European ancestry children NA Illumina [NR] (imputed) 12 FVC change measurement, response to placebo http://www.ebi.ac.uk/efo/EFO_0010339, http://www.ebi.ac.uk/efo/EFO_0008344 GCST009276 Genome-wide genotyping array 2019-10-23 31553412 Legge SE 2019-09-25 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31553412 Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits. Psychotic experience 6,123 European ancestry cases, 121,379 European ancestry controls NA Affymetrix [> 7500000] (imputed) 2 psychotic symptoms http://www.ebi.ac.uk/efo/EFO_0005940 GCST008895 Genome-wide genotyping array 2019-10-23 31553412 Legge SE 2019-09-25 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31553412 Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits. Psychotic experience (multiple occurrences) 3,337 European ancestry cases, 121,379 European ancestry controls NA Affymetrix [> 7500000] (imputed) 0 psychotic symptoms http://www.ebi.ac.uk/efo/EFO_0005940 GCST008897 Genome-wide genotyping array 2019-10-23 31553412 Legge SE 2019-09-25 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31553412 Association of Genetic Liability to Psychotic Experiences With Neuropsychotic Disorders and Traits. Psychotic experience (distressing) 2,143 European ancestry cases, 121,379 European ancestry controls NA Affymetrix [> 7500000] (imputed) 2 psychotic symptoms http://www.ebi.ac.uk/efo/EFO_0005940 GCST008896 Genome-wide genotyping array 2019-09-23 31451708 Hellwege JN 2019-08-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31451708 Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. Estimated glomerular filtration rate in diabetes 70,762 European ancestry individuals, 20,967 African American individuals NA Affymetrix [NR] (imputed) 35 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008746 Genome-wide genotyping array 2019-09-23 31451708 Hellwege JN 2019-08-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31451708 Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. Estimated glomerular filtration rate in non-diabetics 152,624 European ancestry individuals, 36,369 African American individuals NA Affymetrix [NR] (imputed) 98 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008745 Genome-wide genotyping array 2019-09-23 31451708 Hellwege JN 2019-08-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31451708 Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. Estimated glomerular filtration rate 70,762 European ancestry diabetic individuals, 152,624 European ancestry non-diabetic individuals, 20,967 African American diabetic individuals, 36,369 African American non-diabetic individuals 567,401 European ancestry individuals, 165,726 East Asian ancestry individuals, 13,359 South Asian ancestry individuals, 13,842 African American ancestry individuals, 4,961 Hispanic ancestry individuals Affymetrix [NR] (imputed) 188 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008747 Genome-wide genotyping array 2019-10-21 31508503 Warrier V 2019-09-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31508503 Social and non-social autism symptoms and trait domains are genetically dissociable. Autistic traits score (Social and Communication Disorders Checklist) 5,421 European ancestry children NA Illumina [8282911] (imputed) 0 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST008890 Genome-wide genotyping array 2019-10-21 31508503 Warrier V 2019-09-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31508503 Social and non-social autism symptoms and trait domains are genetically dissociable. Systemising 51,564 European ancestry individuals NA NR [9955952] (imputed) 8 systemising measurement http://www.ebi.ac.uk/efo/EFO_0010221 GCST008887 Genome-wide genotyping array 2019-10-21 31508503 Warrier V 2019-09-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31508503 Social and non-social autism symptoms and trait domains are genetically dissociable. Systemising 26,063 European ancestry men NA NR [9955952] (imputed) 4 systemising measurement http://www.ebi.ac.uk/efo/EFO_0010221 GCST008888 Genome-wide genotyping array 2019-10-21 31508503 Warrier V 2019-09-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31508503 Social and non-social autism symptoms and trait domains are genetically dissociable. Systemising 25,501 European ancestry women NA NR [9955952] (imputed) 5 systemising measurement http://www.ebi.ac.uk/efo/EFO_0010221 GCST008889 Genome-wide genotyping array 2019-08-15 26534935 Weng L 2015-11-03 Physiol Genomics www.ncbi.nlm.nih.gov/pubmed/26534935 Genetic loci associated with nonobstructive coronary artery disease in Caucasian women. Nonobstructive coronary artery disease 332 European ancestry female cases, 1,003 European ancestry female controls NA Illumina [52371] 5 non-obstructive coronary artery disease http://www.ebi.ac.uk/efo/EFO_1001483 GCST008436 Targeted genotyping array [Cardio-MetaboChip] 2018-08-23 29934777 Witten A 2018-06-22 J Mol Med (Berl) www.ncbi.nlm.nih.gov/pubmed/29934777 Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study. Heparin-induced thrombocytopenia 96 European ancestry cases, 96 European ancestry heparin-exposed controls 86 European ancestry cases, 86 European ancestry heparin-exposed controls Illumina [~ 351507] 3 response to heparin, Thrombocytopenia http://www.ebi.ac.uk/efo/EFO_0006816, http://purl.obolibrary.org/obo/HP_0001873 GCST006144 Genome-wide genotyping array 2019-08-06 31171785 Dorajoo R 2019-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31171785 Loci for human leukocyte telomere length in the Singaporean Chinese population and trans-ethnic genetic studies. Leukocyte telomere length 16,759 Singaporean Han Chinese ancestry individuals 6,337 Singaporean Chinese ancestry individuals, up to 37,505 European ancestry individuals Illumina [6407959] (imputed) 24 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST008366 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Estimated glomerular filtration rate 567,460 European ancestry individuals, 165,726 East Asian ancestry individuals, 13,842 African American individuals, 13,359 South Asian ancestry individuals, 4,961 Hispanic individuals 216,518 European ancestry individuals, 64,204 non-Hispanic black individuals Affymetrix, Illumina [8221591] (imputed) 307 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008058 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Estimated glomerular filtration rate 567,460 European ancestry individuals 216,518 European ancestry individuals Affymetrix, Illumina [8834748] (imputed) 256 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008059 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Estimated glomerular filtration rate 165,726 East Asian ancestry individuals NA Affymetrix, Illumina [8221591] (imputed) 45 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008060 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Estimated glomerular filtration rate 13,359 South Asian ancestry individuals NA Affymetrix, Illumina [8221591] (imputed) 3 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008061 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Blood urea nitrogen levels 416,178 European and unknown ancestry individuals NA Affymetrix, Illumina [8176554] (imputed) 132 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST008062 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Blood urea nitrogen levels 243,029 European ancestry individuals NA Affymetrix, Illumina [8358347] (imputed) 0 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST008063 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Chronic kidney disease 64,164 European and unknown ancestry cases, 561,055 European and unknown ancestry controls NA Affymetrix, Illumina [9585923] (imputed) 47 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST008064 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Chronic kidney disease up to 64,164 European ancestry cases, up to 561,055 European ancestry controls NA Affymetrix, Illumina [9585923] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST008065 Genome-wide genotyping array 2019-07-05 31152163 Wuttke M 2019-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31152163 A catalog of genetic loci associated with kidney function from analyses of a million individuals. Estimated glomerular filtration rate 13,842 African American individuals NA Affymetrix, Illumina [8221591] (imputed) 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008066 Genome-wide genotyping array 2019-05-28 30510241 Huyghe JR 2018-12-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30510241 Discovery of common and rare genetic risk variants for colorectal cancer. Colorectal cancer or advanced adenoma 55,105 European ancestry cases, 3,026 East Asian ancestry cases, 65,079 European ancestry controls, 2,268 East Asian ancestry controls NA Affymetrix, Illumina [16900397] (imputed) 121 colorectal cancer, colorectal adenoma http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0005406 GCST007856 Genome-wide genotyping array 2022-06-22 30510241 Huyghe JR 2018-12-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30510241 Discovery of common and rare genetic risk variants for colorectal cancer. Colorectal cancer 4,439 European ancestry cases, 4,115 European ancestry controls NA Illumina [12477546] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012880 Genome-wide genotyping array 2022-06-22 30510241 Huyghe JR 2018-12-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30510241 Discovery of common and rare genetic risk variants for colorectal cancer. Colorectal cancer 19,948 European ancestry cases, 12,124 European ancestry controls NA Affymetrix, Illumina [39216056] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012879 Genome-wide genotyping array 2022-06-22 30510241 Huyghe JR 2018-12-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30510241 Discovery of common and rare genetic risk variants for colorectal cancer. Colorectal cancer 1,460 European ancestry cases, 774 European ancestry controls NA Affymetrix [11559203] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012878 Genome-wide genotyping array 2022-06-22 30510241 Huyghe JR 2018-12-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30510241 Discovery of common and rare genetic risk variants for colorectal cancer. Colorectal cancer 11,835 European ancestry cases, 11,856 European ancestry controls NA Illumina [12366131] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012877 Genome-wide genotyping array 2022-06-22 30510241 Huyghe JR 2018-12-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30510241 Discovery of common and rare genetic risk variants for colorectal cancer. Colorectal cancer 11,895 European ancestry cases, 14,659 European ancestry controls NA Affymetrix, Illumina [39232598] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012876 Genome-wide genotyping array 2018-08-16 29921221 Cha S 2018-06-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/29921221 Identification of five novel genetic loci related to facial morphology by genome-wide association studies. Facial morphology 5,643 Korean ancestry individuals 1,926 Korean ancestry individuals Affymetrix [311944] 8 facial morphology http://www.ebi.ac.uk/efo/EFO_0004743 GCST006108 Genome-wide genotyping array 2018-08-16 29921221 Cha S 2018-06-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/29921221 Identification of five novel genetic loci related to facial morphology by genome-wide association studies. Forehead morphology 5,643 Korean ancestry individuals 1,926 Korean ancestry individuals Affymetrix [311944] 6 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST006106 Genome-wide genotyping array 2018-08-16 29921221 Cha S 2018-06-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/29921221 Identification of five novel genetic loci related to facial morphology by genome-wide association studies. Eye morphology 5,643 Korean ancestry individuals 1,926 Korean ancestry individuals Affymetrix [311944] 12 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST006105 Genome-wide genotyping array 2018-08-16 29921221 Cha S 2018-06-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/29921221 Identification of five novel genetic loci related to facial morphology by genome-wide association studies. Nose morphology 5,643 Korean ancestry individuals up to 1,940 Korean ancestry individuals Affymetrix [311944] 38 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006110 Genome-wide genotyping array 2018-08-16 29921221 Cha S 2018-06-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/29921221 Identification of five novel genetic loci related to facial morphology by genome-wide association studies. Lip morphology 5,643 Korean ancestry individuals 1,926 Korean ancestry individuals Affymetrix [311944] 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST006109 Genome-wide genotyping array 2018-08-16 29921221 Cha S 2018-06-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/29921221 Identification of five novel genetic loci related to facial morphology by genome-wide association studies. Upper eyelid morphology 5,643 Korean ancestry individuals 1,926 Korean ancestry individuals Affymetrix [311944] 16 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST006107 Genome-wide genotyping array 2017-04-10 28039263 Wheeler HE 2016-12-30 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/28039263 Variants in WFS1 and Other Mendelian Deafness Genes Are Associated with Cisplatin-Associated Ototoxicity. Cisplatin-induced ototoxicity 511 European ancestry testicular cancer survivor individuals 238 children Illumina [5060354] (imputed) 20 ototoxicity, response to cisplatin http://www.ebi.ac.uk/efo/EFO_0006951, http://purl.obolibrary.org/obo/GO_0072718 GCST003898 Genome-wide genotyping array 2017-05-12 28045058 Kim SW 2017-01-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28045058 Identification of genetic susceptibility loci for intestinal Behçet's disease. Behcet's disease 99 Korean ancestry cases with intestinal involvement, 100 Korean ancestry cases without intestinal involvement, 597 Korean ancestry controls. 196 Korean ancestry cases with intestinal involvement, 138 Korean ancestry cases without intestinal involvement, 391 Korean ancestry controls. Affymetrix [5418765] (imputed) 0 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST004019 Genome-wide genotyping array 2017-05-24 28065765 Nagao Y 2017-01-05 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/28065765 Genome-Wide Association Study Identifies Risk Variants for Lichen Planus in Patients With Hepatitis C Virus Infection. Lichen planus in hepatitis C 71 Japanese ancestry cases, 190 Japanese ancestry controls 38 Italian ancestry cases, 7 Italian ancestry controls Affymetrix [629553] 0 lichen planus http://www.ebi.ac.uk/efo/EFO_1000726 GCST004090 Genome-wide genotyping array 2018-09-06 29898447 Alaraudanjoki VK 2018-06-13 Caries Res www.ncbi.nlm.nih.gov/pubmed/29898447 Genome-Wide Association Study of Erosive Tooth Wear in a Finnish Cohort. Erosive tooth wear (severe vs non-severe) 86 Finnish ancestry male severe erosion cases, 50 Finnish ancestry female severe erosion cases, 817 Finnish ancestry male non-severe erosion controls, 991 Finnish ancestry female non-severe erosion controls NA Illumina [NR] (imputed) 136 erosive tooth wear measurement http://www.ebi.ac.uk/efo/EFO_0009331 GCST006218 Genome-wide genotyping array 2018-09-06 29898447 Alaraudanjoki VK 2018-06-13 Caries Res www.ncbi.nlm.nih.gov/pubmed/29898447 Genome-Wide Association Study of Erosive Tooth Wear in a Finnish Cohort. Erosive tooth wear (severe vs none or mild) 136 Finnish ancestry severe erosion cases, 1011 Finnish ancestry mild or no erosion controls NA Illumina [NR] (imputed) 23 erosive tooth wear measurement http://www.ebi.ac.uk/efo/EFO_0009331 GCST006226 Genome-wide genotyping array 2019-04-25 30467376 Wilker S 2018-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30467376 Genetic variation is associated with PTSD risk and aversive memory: Evidence from two trauma-Exposed African samples and one healthy European sample. Post-traumatic stress disorder 924 Sub-Saharan African ancestry individuals 371 Sub-Saharan African ancestry individuals Affymetrix [654099] 0 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST007651 Genome-wide genotyping array 2018-08-23 29915124 Marini S 2018-06-18 Stroke www.ncbi.nlm.nih.gov/pubmed/29915124 17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage. Hematoma volume in lobar spontaneous intracerebral hemorrhage 228 European ancestry cases 71 European ancestry cases Illumina [7567631] (imputed) 1 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST006139 Genome-wide genotyping array 2018-08-23 29915124 Marini S 2018-06-18 Stroke www.ncbi.nlm.nih.gov/pubmed/29915124 17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage. Hematoma volume in non-lobar spontaneous intracerebral hemorrhage 166 European ancestry cases 169 European ancestry cases Illumina [7569876] (imputed) 1 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST006140 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived sweetness of sucrose 686 European ancestry twins NA Illumina [5833901] (imputed) 13 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008760 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Sucrose liking 686 European ancestry twins NA Illumina [5833901] (imputed) 12 sucrose liking measurement http://www.ebi.ac.uk/efo/EFO_0010157 GCST008761 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Intake of sweets 21,447 European ancestry individuals NA Affymetrix [10353649] (imputed) 13 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST008762 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived intensity of fructose 1,757 European ancestry twins NA Illumina [4381914] (imputed) 3 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008763 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived intensity of neohesperidin dihydrochalcone 1,757 European ancestry twins NA Illumina [4381914] (imputed) 12 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008764 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived intensity of aspartame 1,757 European ancestry twins NA Illumina [4381914] (imputed) 5 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008765 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived intensity of sweet substances 1,757 European ancestry twins NA Illumina [4381914] (imputed) 3 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008766 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived intensity of sucrose 686 European ancestry twins NA Illumina [5833901] (imputed) 9 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008767 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived intensity of sweet substances 2,443 European ancestry twins NA Illumina [4001140] (imputed) 4 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008768 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Intake of total sugars 174,424 European ancestry individuals NA Affymetrix [10353649] (imputed) 53 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST008759 Genome-wide genotyping array 2019-09-25 31005972 Hwang LD 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005972 New insight into human sweet taste: a genome-wide association study of the perception and intake of sweet substances. Perceived intensity of glucose 1,757 European ancestry twins NA Illumina [4381914] (imputed) 7 sensory perception of sweet taste http://purl.obolibrary.org/obo/GO_0050916 GCST008769 Genome-wide genotyping array 2019-10-10 31497858 Dumitrescu L 2019-09-01 Brain www.ncbi.nlm.nih.gov/pubmed/31497858 Sex differences in the genetic predictors of Alzheimer's pathology. Neuritic plaque 2,701 European ancestry men, 3,275 European ancestry women NA Affymetrix, Illumina [NR] (imputed) 11 neuritic plaque measurement http://www.ebi.ac.uk/efo/EFO_0006798 GCST008829 Genome-wide genotyping array 2019-10-09 31497858 Dumitrescu L 2019-09-01 Brain www.ncbi.nlm.nih.gov/pubmed/31497858 Sex differences in the genetic predictors of Alzheimer's pathology. Neurofibrillary tangles 2,701 European ancestry men NA Affymetrix, Illumina [NR] (imputed) 13 neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006797 GCST008821 Genome-wide genotyping array 2019-10-10 31497858 Dumitrescu L 2019-09-01 Brain www.ncbi.nlm.nih.gov/pubmed/31497858 Sex differences in the genetic predictors of Alzheimer's pathology. Neurofibrillary tangles 3,275 European ancestry women NA Affymetrix, Illumina [NR] (imputed) 19 neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006797 GCST008830 Genome-wide genotyping array 2019-10-09 31497858 Dumitrescu L 2019-09-01 Brain www.ncbi.nlm.nih.gov/pubmed/31497858 Sex differences in the genetic predictors of Alzheimer's pathology. Neuritic plaque 2,701 European ancestry men NA Affymetrix, Illumina [NR] (imputed) 9 neuritic plaque measurement http://www.ebi.ac.uk/efo/EFO_0006798 GCST008822 Genome-wide genotyping array 2018-05-30 29545352 Li Y 2018-03-15 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29545352 Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. Serum metabolite concentrations in chronic kidney disease 1,143 European ancestry cases NA Illumina [up to 9281895] (imputed) 40 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST005648 Genome-wide genotyping array 2018-05-30 29545352 Li Y 2018-03-15 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29545352 Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. Urinary metabolite ratios in chronic kidney disease 1,143 European ancestry cases NA Illumina [up to 9281895] (imputed) 14 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST005649 Genome-wide genotyping array 2018-05-30 29545352 Li Y 2018-03-15 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29545352 Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. Serum metabolite ratios in chronic kidney disease 1,143 European ancestry cases NA Illumina [up to 9281895] (imputed) 259 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST005650 Genome-wide genotyping array 2018-05-30 29545352 Li Y 2018-03-15 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29545352 Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. Urinary metabolite levels in chronic kidney disease 1,143 European ancestry cases NA Illumina [up to 9281895] (imputed) 9 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST005651 Genome-wide genotyping array 2018-06-04 29545352 Li Y 2018-03-15 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29545352 Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. Fractional excretion of metabolites in chronic kidney disease 1,143 European ancestry cases NA Illumina [up to 9281895] (imputed) 4 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST005666 Genome-wide genotyping array 2017-06-02 28081215 Pardo LM 2017-01-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/28081215 Genome-Wide Association Studies of Multiple Keratinocyte Cancers. Multiple keratinocyte cancers 2,106 European ancestry multiple keratinocyte cancer cases, 2,061 European ancestry single keratinocyte cancer cases, 135 European and unknown ancestry multiple keratinocyte cancer cases, 761 European and unknown ancestry single keratinocyte cancer cases NA Affymetrix, Illumina [up to 9001799] (imputed) 17 squamous cell carcinoma, multiple keratinocyte carcinoma susceptibility measurement, basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707, http://www.ebi.ac.uk/efo/EFO_0007932, http://www.ebi.ac.uk/efo/EFO_0004193 GCST004134 Genome-wide genotyping array 2017-05-17 28084903 Hallberg P 2017-01-13 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/28084903 Genetic variants associated with angiotensin-converting enzyme inhibitor-induced cough: a genome-wide association study in a Swedish population. Cough in response to angiotensin-converting enzyme inhibitor drugs 123 European ancestry cases, 1,345 European and unknown ancestry controls, 1 Middle Eastern ancestry case NR Illumina [8600000] (imputed) 32 response to angiotensin-converting enzyme inhibitor, Cough http://www.ebi.ac.uk/efo/EFO_0005325, http://purl.obolibrary.org/obo/HP_0012735 GCST004049 Genome-wide genotyping array 2017-04-11 28078323 Raj T 2016-12-21 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/28078323 Genetic architecture of age-related cognitive decline in African Americans. Cognitive decline (age-related) 3,964 African American ancestry individuals. NA Illumina [13900000] (imputed) 20 Mental deterioration http://purl.obolibrary.org/obo/HP_0001268 GCST003901 Genome-wide genotyping array 2017-01-27 27523435 Mosteller M 2016-07-05 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/27523435 No evidence of large genetic effects on steroid response in asthma patients. Response to inhaled corticosteroid treatment in asthma (change in FEV1) 2,672 cases NA Illumina [~ 9800000] (imputed) 0 FEV change measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0031960 GCST003567 Genome-wide genotyping array 2017-04-21 28041642 Carmona FD 2016-12-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/28041642 A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis. Giant cell arteritis 2,134 European ancestry cases, 9,125 European ancestry controls NA Illumina [1844133] (imputed) 5 temporal arteritis http://www.ebi.ac.uk/efo/EFO_1001209 GCST003928 Genome-wide genotyping array 2017-05-16 28070124 Meyers JL 2017-01-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28070124 An endophenotype approach to the genetics of alcohol dependence: a genome wide association study of fast beta EEG in families of African ancestry. Fast beta electroencephalogram 2,382 African American individuals NA Illumina [12972748] (imputed) 1 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST004048 Genome-wide genotyping array 2019-01-14 30367059 Teumer A 2018-10-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30367059 Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Free thyroxine concentration 49,269 European ancestry individuals up to 22,383 European ancestry individuals Affymetrix, Illumina [8048941] (imputed) 19 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST006896 Genome-wide genotyping array 2019-01-14 30367059 Teumer A 2018-10-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30367059 Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Thyroid stimulating hormone levels 54,288 European ancestry individuals up to 22,383 European ancestry individuals Affymetrix, Illumina [8048941] (imputed) 22 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST006899 Genome-wide genotyping array 2019-01-14 30367059 Teumer A 2018-10-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30367059 Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Hypothyroidism 3,340 European ancestry cases, 49,983 European ancestry controls NA Affymetrix, Illumina [5965951] (imputed) 8 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST006898 Genome-wide genotyping array 2019-01-14 30367059 Teumer A 2018-10-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30367059 Genome-wide analyses identify a role for SLC17A4 and AADAT in thyroid hormone regulation. Hyperthyroidism 1,840 European ancestry cases, 49,983 European ancestry controls NA Affymetrix, Illumina [5965951] (imputed) 9 hyperthyroidism http://www.ebi.ac.uk/efo/EFO_0009189 GCST006897 Genome-wide genotyping array 2019-04-12 29785011 Zhu Z 2018-05-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29785011 A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. Asthma 14,085 European ancestry cases, 76,768 European ancestry controls 10,365 cases, 16,110 controls Affymetrix [74888535] (imputed) 6 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007562 Genome-wide genotyping array 2019-04-12 29785011 Zhu Z 2018-05-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29785011 A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. Allergic disease (asthma, hay fever or eczema) 25,685 European ancestry allergic diseases cases, 76,768 European ancestry controls NA Affymetrix [74888535] (imputed) 33 asthma, allergic disease http://purl.obolibrary.org/obo/MONDO_0004979, http://purl.obolibrary.org/obo/MONDO_0005271 GCST007563 Genome-wide genotyping array 2019-04-12 29785011 Zhu Z 2018-05-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29785011 A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. Asthma or allergic disease (pleiotropy) 14,085 European asthma cases, 25,685 European ancestry allergic diseases cases, 76,768 European ancestry controls NA NR [74888535] (imputed) 38 asthma, allergic disease http://purl.obolibrary.org/obo/MONDO_0004979, http://purl.obolibrary.org/obo/MONDO_0005271 GCST007564 Genome-wide genotyping array 2019-03-25 30745170 Strawbridge RJ 2019-02-07 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/30745170 Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide. Deliberate self-harm 100,234 British ancestry individuals NA Affymetrix [9481578] (imputed) 1 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST007391 Genome-wide genotyping array 2019-03-25 30745170 Strawbridge RJ 2019-02-07 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/30745170 Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide. Suicidality (suicidal ideation/attempts) 108,090 British ancestry individuals NA Affymetrix [9481578] (imputed) 1 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST007390 Genome-wide genotyping array 2019-03-25 30745170 Strawbridge RJ 2019-02-07 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/30745170 Identification of novel genome-wide associations for suicidality in UK Biobank, genetic correlation with psychiatric disorders and polygenic association with completed suicide. Suicidality 122,808 British ancestry individuals NA Affymetrix [9481578] (imputed) 3 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST007389 Genome-wide genotyping array 2019-10-16 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (depressed mood) (binary trait) 32,263 European ancestry cases, 116,489 European ancestry controls NA NR [9413637] (imputed) 1 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008840 Genome-wide genotyping array 2019-10-16 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (sleep problems) (binary trait) 72,302 European ancestry cases, 76,450 European ancestry controls NA NR [9413637] (imputed) 3 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008841 Genome-wide genotyping array 2019-10-16 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (fatigue) (binary trait) 73,924 European ancestry cases, 74,828 European ancestry controls NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008842 Genome-wide genotyping array 2019-10-16 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (appetite changes) (binary trait) 26,757 European ancestry cases, 121,995 European ancestry controls NA NR [9413637] (imputed) 1 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008843 Genome-wide genotyping array 2019-10-16 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (low self-esteem) (binary trait) 28,206 European ancestry cases, 120,546 European ancestry controls NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008844 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (concentration problems) (binary trait) 26,229 European ancestry cases, 122,523 European ancestry controls NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008845 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (psychomotor changes) (binary trait) 7,914 European ancestry cases, 140,838 European ancestry controls NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008846 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (suicidal ideation) (binary trait) 6,064 European ancestry cases, 142,688 European ancestry controls NA NR [9413637] (imputed) 0 suicide ideation measurement http://www.ebi.ac.uk/efo/EFO_0007619 GCST008847 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptoms (binary sum-score) 148,752 European ancestry individuals NA NR [9413637] (imputed) 4 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008849 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptoms (sum-score) 148,752 European ancestry individuals NA NR [9413637] (imputed) 2 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008848 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (sleep problems) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008850 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (fatigue) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 5 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008851 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (appetite changes) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008852 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (low self-esteem) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 1 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008853 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (concentration problems) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008854 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (psychomotor changes) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008855 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (suicidal ideation) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 0 suicide ideation measurement http://www.ebi.ac.uk/efo/EFO_0007619 GCST008856 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (anhedonia) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 2 anhedonia measurement http://www.ebi.ac.uk/efo/EFO_0009587 GCST008857 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (depressed mood) (ordinal trait) 148,752 European ancestry individuals NA NR [9413637] (imputed) 1 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST008858 Genome-wide genotyping array 2019-10-17 31530331 Thorp JG 2019-09-18 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31530331 Genetic heterogeneity in self-reported depressive symptoms identified through genetic analyses of the PHQ-9. Depressive symptom (anhedonia) (binary trait) 27,288 European ancestry cases, 121,464 European ancestry controls NA NR [9413637] (imputed) 2 anhedonia measurement http://www.ebi.ac.uk/efo/EFO_0009587 GCST008859 Genome-wide genotyping array 2017-01-24 27519822 Power RA 2016-05-24 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/27519822 Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium. Major depressive disorder 3,869 European ancestry 50% oldest-onset cases, 5,051 European ancestry cases, 2,691 European ancestry controls, 6,828 unknown controls 6,107 European ancestry, Han Chinese ancestry and unknown ancestry 50% oldest-onset cases, 7,131 European ancestry, Han Chinese ancestry and unknown ancestry cases, 104,402 European ancestry controls, 5,537 Han Chinese ancestry controls, 14,291 unknown ancestry controls NR [1235109] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST003558 Genome-wide genotyping array 2017-03-31 27531626 Polimanti R 2016-08-17 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/27531626 The Interplay Between Risky Sexual Behaviors and Alcohol Dependence: Genome-Wide Association and Neuroimaging Support for LHPP as a Risk Gene. Risky sexual behaviors (alcohol dependence interaction) 1,541 African American alcohol dependent cases, 1,436 European American alcohol dependent cases, 632 African American non-alcohol dependent controls, 315 European American non-alcohol dependent controls NA Illumina [at least 988306] (imputed) 1 behavioural disinhibition measurement, alcohol dependence, risky sexual behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006946, http://purl.obolibrary.org/obo/MONDO_0007079, http://www.ebi.ac.uk/efo/EFO_0007877 GCST003860 Genome-wide genotyping array 2019-04-03 30429480 Duffy DL 2018-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30429480 Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nevus count or cutaneous melanoma 52,506 European ancestry individuals, 12,874 European ancestry cases, 23,203 European ancestry controls NA Affymetrix, Illumina [7850345] (imputed) 30 nevus count, cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0004632, http://www.ebi.ac.uk/efo/EFO_0000389 GCST007505 Genome-wide genotyping array 2019-04-03 30429480 Duffy DL 2018-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30429480 Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways. Nevus count 52,506 European ancestry individuals NA Affymetrix, Illumina [up to 31337615] (imputed) 12 nevus count http://www.ebi.ac.uk/efo/EFO_0004632 GCST007504 Genome-wide genotyping array 2017-05-12 28081371 Sanders AE 2017-01-12 J Dent Res www.ncbi.nlm.nih.gov/pubmed/28081371 GWAS Identifies New Loci for Painful Temporomandibular Disorder: Hispanic Community Health Study/Study of Latinos. Temporomandibular joint disorder 769 Hispanic cases, 9,384 Hispanic controls 768 European ancestry cases, 4,845 European ancestry controls, 144 Hispanic/Latin American cases, 492 Hispanic/Latin American controls, 999 cases, 2,031 controls Illumina [2100000] (imputed) 5 temporomandibular joint disorder http://www.ebi.ac.uk/efo/EFO_0005279 GCST004034 Genome-wide genotyping array 2019-08-07 31152121 Zhu M 2019-05-31 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/31152121 Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study. Type 1 diabetes 1,005 Han Chinese ancestry cases, 1,257 Han Chinese ancestry controls 1,378 Han Chinese ancestry cases, 3,774 Han Chinese ancestry controls Illumina [787224] (imputed) 5 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST008377 Genome-wide genotyping array 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking behaviour (age at first cigarette) up to 2,705 African ancestry individuals NA Illumina [~ 250000] (imputed) 0 time to first cigarette measurement http://www.ebi.ac.uk/efo/EFO_0010126 GCST008807 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking behaviour (cigarettes smoked per day) up to 2,685 African ancestry individuals NA Illumina [~ 250000] (imputed) 1 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST008804 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Alcohol consumption (drinks per week) up to 7,594 African ancestry individuals NA Illumina [~ 250000] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST008805 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking behaviour (cigarette pack-years) up to 2,658 African ancestry individuals NA Illumina [~ 250000] (imputed) 0 tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0009115 GCST008808 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking initiation (ever regular vs never regular) up to 8,974 African ancestry individuals NA Illumina [~ 250000] (imputed) 0 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST008806 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking behaviour (age at first cigarette) up to 146,117 European ancestry control NA Illumina [~ 250000] (imputed) 3 time to first cigarette measurement http://www.ebi.ac.uk/efo/EFO_0010126 GCST008802 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking behaviour (cigarettes smoked per day) up to 153,918 European ancestry individuals NA Illumina [~ 250000] (imputed) 12 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST008809 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking behaviour (cigarette pack-years) up to 150,993 European ancestry individuals NA Illumina [~ 250000] (imputed) 17 tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0009115 GCST008803 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Smoking initiation (ever regular vs never regular) up to 433,216 European ancestry individuals NA Illumina [~ 250000] (imputed) 97 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST008810 Exome genotyping array [Exome array] 2019-10-04 30679032 Brazel DM 2018-12-06 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30679032 Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use. Alcohol consumption (drinks per week) up to 357,854 European ancestry individuals NA Illumina [~ 250000] (imputed) 47 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST008811 Exome genotyping array [Exome array] 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. Estradiol levels 4,191 European ancestry men, 2,607 European ancestry women NA Affymetrix [up to 8900000] (imputed) 10 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST008881 Genome-wide genotyping array 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. Cortisol levels (plasma) 4,301 European ancestry men, 3,366 European ancestry women NA Affymetrix [up to 8900000] (imputed) 3 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST008882 Genome-wide genotyping array 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. DHEAS levels 4,301 European ancestry men, 3,358 European ancestry women NA Affymetrix [up to 8900000] (imputed) 63 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST008883 Genome-wide genotyping array 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. Testosterone levels 4,291 European ancestry men, 3,352 European ancestry women NA Affymetrix [up to 8900000] (imputed) 15 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST008884 Genome-wide genotyping array 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. Progesterone levels 1,358 European ancestry men, 1,261 European ancestry women NA Affymetrix [up to 8900000] (imputed) 12 progesterone measurement http://www.ebi.ac.uk/efo/EFO_0007004 GCST008885 Genome-wide genotyping array 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. 17-hydroxyprogesterone (17-OHP) levels 1,358 European ancestry men, 712 European ancestry women NA Affymetrix [up to 8900000] (imputed) 37 17-hydroxyprogesterone measurement http://www.ebi.ac.uk/efo/EFO_0010220 GCST008879 Genome-wide genotyping array 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. Androstenedione levels 1,358 European ancestry men, 712 European ancestry women NA Affymetrix [up to 8900000] (imputed) 5 androstenedione measurement http://www.ebi.ac.uk/efo/EFO_0007972 GCST008886 Genome-wide genotyping array 2019-10-21 31169883 Pott J 2019-06-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31169883 Genetic association study of eight steroid hormones and implications for sexual dimorphism of coronary artery disease. Aldosterone levels 1,307 European ancestry men, 686 European ancestry women NA Affymetrix [up to 8900000] (imputed) 0 aldosterone measurement http://www.ebi.ac.uk/efo/EFO_0010219 GCST008880 Genome-wide genotyping array 2019-10-02 28330615 Rhinn H 2017-03-18 Cell Syst www.ncbi.nlm.nih.gov/pubmed/28330615 Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes. Differential aging in older adults (frontal cortex) 413 individuals 497 individuals NR [468129] 1 obsolete aging, brain measurement http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004464 GCST008795 Genome-wide genotyping array 2019-10-02 28330615 Rhinn H 2017-03-18 Cell Syst www.ncbi.nlm.nih.gov/pubmed/28330615 Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes. Differential aging in younger adults (frontal cortex) 303 individuals NA NR [468129] 0 obsolete aging, brain measurement http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004464 GCST008796 Genome-wide genotyping array 2019-10-02 28330615 Rhinn H 2017-03-18 Cell Syst www.ncbi.nlm.nih.gov/pubmed/28330615 Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes. Differential aging (cerebellum) 716 individuals 497 individuals NR [468129] 0 obsolete aging, brain measurement http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004464 GCST008797 Genome-wide genotyping array 2019-10-02 28330615 Rhinn H 2017-03-18 Cell Syst www.ncbi.nlm.nih.gov/pubmed/28330615 Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes. Differential aging in older adults (cerebellum) 413 individuals 497 individuals NR [468129] 0 obsolete aging, brain measurement http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004464 GCST008798 Genome-wide genotyping array 2019-10-02 28330615 Rhinn H 2017-03-18 Cell Syst www.ncbi.nlm.nih.gov/pubmed/28330615 Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes. Differential aging (frontal cortex) 303 individuals NA NR [468129] 0 obsolete aging, brain measurement http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004464 GCST008799 Genome-wide genotyping array 2019-10-02 28330615 Rhinn H 2017-03-18 Cell Syst www.ncbi.nlm.nih.gov/pubmed/28330615 Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes. Differential aging (frontal cortex) 716 individuals 497 individuals NR [468129] 1 obsolete aging, brain measurement http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004464 GCST008800 Genome-wide genotyping array 2017-05-31 28077804 Ben-Avraham D 2017-01-10 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/28077804 The complex genetics of gait speed: genome-wide meta-analysis approach. Gait speed in old age 31,478 European ancestry older adults 2,588 European ancestry older adults Affymetrix, Illumina [~ 2500000] (imputed) 19 gait measurement http://www.ebi.ac.uk/efo/EFO_0007680 GCST004110 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Oxygen saturation of hemoglobin levels 921 Tibetan ancestry individuals NA Illumina [3507568] (imputed) 0 oxygen saturation measurement http://www.ebi.ac.uk/efo/EFO_0005682 GCST006745 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Pulse rate 921 Tibetan ancestry individuals NA Illumina [3508046] (imputed) 0 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST006746 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Oxygenated hemoglobin levels 920 Tibetan ancestry individuals NA Illumina [3507568] (imputed) 1 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST006747 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Deoxygenated hemoglobin levels 921 Tibetan ancestry individuals NA Illumina [3507568] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST006748 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child death (Number of children surviving at 1 year but died <5 years) 849 Tibetan ancestry individuals NA Illumina [3507585] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006749 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child death in continuous marriage (Number of children surviving at 1 year but died <5 years) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006750 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child survival (Number of children surviving at 5 years) 849 Tibetan ancestry individuals NA Illumina [3507585] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006751 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child survival in continuous marriage (Number of children surviving at 5 years) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006752 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child death (Proportion of children surviving at 1 year but died <5 years) 849 Tibetan ancestry individuals NA Illumina [3507585] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006753 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child death in continuous marriage (Proportion of children surviving at 1 year but died <5 years) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006754 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child survival (Proportion of children surviving at 5 years) 849 Tibetan ancestry individuals NA Illumina [3507585] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006755 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Child survival in continuous marriage (Proportion of children surviving at 5 years) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006756 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile death (Number of children surviving at 5 years but died <15 years) 531 Tibetan ancestry individuals NA Illumina [3506695] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006757 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile death in continuous marriage (Number of children surviving at 5 years but died <15 years) up to 531 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006758 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile death (Proportion of children surviving at 5 years but died <15 years) 531 Tibetan ancestry individuals NA Illumina [3507249] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006759 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile death in continuous marriage (Proportion of children surviving at 5 years but died <15 years) up to 531 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006760 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile survival (Number of children surviving at 15 years) 531 Tibetan ancestry individuals NA Illumina [3506695] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006761 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile survival in continuous marriage (Number of children surviving at 15 years) up to 531 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006762 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile survival (Proportion of children surviving at 15 years) 531 Tibetan ancestry individuals NA Illumina [3507249] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006763 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Juvenile survival in continuous marriage (Proportion of children surviving at 15 years) up to 531 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006764 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of live births 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 1 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006765 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of live births in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006766 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Proportion of live births 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006767 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Proportion of live births in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006768 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of pregnancies 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 1 number of pregnancies measurement http://www.ebi.ac.uk/efo/EFO_0009438 GCST006771 Genome-wide genotyping array 2019-01-08 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant death in continuous marriage (Proportion of children died <1 year) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006859 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Hemoglobin levels 921 Tibetan ancestry individuals NA Illumina [3507568] (imputed) 1 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST006720 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant and Child death (Number of children died <5 years) 849 Tibetan ancestry individuals NA Illumina [3507585] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006721 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant and Child death in continuous marriage (Number of children died <5 years) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006722 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant and Child death (Proportion of children died <5 years) 849 Tibetan ancestry individuals NA Illumina [3507585] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006723 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant and Child death in continuous marriage (Proportion of children died <5 years) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006724 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant, child and juvenile death (number of children died <15 years) 532 Tibetan ancestry individuals NA Illumina [3506123] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006725 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant, child and juvenile death in continuous marriage (number of children died <15 years) up to 532 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006726 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant, child and juvenile death (proportion of children died <15 years) 532 Tibetan ancestry individuals NA Illumina [3506123] (imputed) 1 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006727 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant, child and juvenile death in continuous marriage (proportion of children died <15 years) up to 532 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 1 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006730 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant death (Number of children died <1 year) 923 Tibetan ancestry individuals NA Illumina [3507108] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006728 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant death in continuous marriage (Number of children died <1 year) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006729 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant death (Proportion of children died <1 year) 923 Tibetan ancestry individuals NA Illumina [3507108] (imputed) 0 offspring mortality measurement http://www.ebi.ac.uk/efo/EFO_0009437 GCST006731 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant survival (Number of children surviving at 1 year) 923 Tibetan ancestry individuals NA Illumina [3507108] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006733 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant survival in continuous marriage (Number of children surviving at 1 year) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006734 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant survival (Proportion of children surviving at 1 year) 923 Tibetan ancestry individuals NA Illumina [3507108] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006735 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Infant survival in continuous marriage (Proportion of children surviving at 1 year) 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 offspring survival measurement http://www.ebi.ac.uk/efo/EFO_0009436 GCST006736 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of miscarriages 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006737 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of miscarriages in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006738 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Proportion of miscarriages 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006739 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Proportion of miscarriages in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006740 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of stillbirths 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006741 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of stillbirths in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 1 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006742 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Proportion of stillbirths 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006743 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Proportion of stillbirths in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST006744 Genome-wide genotyping array 2021-12-06 31033190 Singh S 2019-04-29 Clin Transl Sci www.ncbi.nlm.nih.gov/pubmed/31033190 Genomic Association Analysis Reveals Variants Associated with Blood Pressure Response to Beta-Blockers in European Americans. Response to beta blocker use in hypertension (diastolic blood pressure) 201 European ancestry individuals 440 European ancestry individuals Illumina [2500000] (imputed) 0 diastolic blood pressure change measurement, response to beta blocker http://www.ebi.ac.uk/efo/EFO_0006945, http://www.ebi.ac.uk/efo/EFO_0007766 GCST012578 Genome-wide genotyping array 2021-12-06 31033190 Singh S 2019-04-29 Clin Transl Sci www.ncbi.nlm.nih.gov/pubmed/31033190 Genomic Association Analysis Reveals Variants Associated with Blood Pressure Response to Beta-Blockers in European Americans. Response to beta blocker use in hypertension (diastolic blood pressure) 201 European ancestry individuals 440 European ancestry individuals Illumina [2500000] (imputed) 0 diastolic blood pressure change measurement, hypertension, response to beta blocker http://www.ebi.ac.uk/efo/EFO_0006945, http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0007766 GCST012577 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of pregnancies in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 number of pregnancies measurement http://www.ebi.ac.uk/efo/EFO_0009438 GCST006772 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of twin births 981 Tibetan ancestry individuals NA Illumina [3507697] (imputed) 0 multiple births measurement http://www.ebi.ac.uk/efo/EFO_0009439 GCST006773 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Number of twin births in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 multiple births measurement http://www.ebi.ac.uk/efo/EFO_0009439 GCST006774 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Age at last pregnancy 958 Tibetan ancestry individuals NA Illumina [3507463] (imputed) 0 age at last pregnancy measurement http://www.ebi.ac.uk/efo/EFO_0009440 GCST006775 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Age at last pregnancy in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 age at last pregnancy measurement http://www.ebi.ac.uk/efo/EFO_0009440 GCST006776 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Age at first birth 972 Tibetan ancestry individuals NA Illumina [3507330] (imputed) 0 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST006769 Genome-wide genotyping array 2018-12-14 30188897 Jeong C 2018-09-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30188897 Detecting past and ongoing natural selection among ethnically Tibetan women at high altitude in Nepal. Age at first birth in continuous marriage 593 Tibetan ancestry individuals NA Illumina [~ 3500000] (imputed) 0 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST006770 Genome-wide genotyping array 2019-03-19 30604766 Morris AP 2019-01-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30604766 Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies. Estimated glomerular filtration rate 134,070 European ancestry individuals, 143,658 East Asian ancestry individuals, 26,344 Hispanic or Latino ancestry individuals, 8,224 African American individuals NA Affymetrix, Illumina [at least 5248638] (imputed) 136 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST007344 Genome-wide genotyping array 2019-11-15 30420678 Tasa T 2018-11-12 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30420678 Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. Adverse response to drug 16,226 European ancestry individuals NA Illumina [16500000] (imputed) 61 adverse effect, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0009658, http://purl.obolibrary.org/obo/GO_0009410 GCST009028 Genome-wide genotyping array 2020-01-06 31609978 Huang L 2019-10-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31609978 Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft. Nonsyndromic cleft lip 945 Southern Han Chinese ancestry cases, 5,048 Southern Han Chinese ancestry controls 1,273 Han Chinese ancestry cases, 5,097 Han Chinese ancestry controls Illumina [at least 870261] (imputed) 15 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST009357 Genome-wide genotyping array 2020-01-06 31609978 Huang L 2019-10-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31609978 Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft. Nonsyndromic cleft palate 930 Southern Han Chinese ancestry cases, 5,048 Southern Han Chinese ancestry controls 1,141 Han Chinese ancestry cases, 5,097 Han Chinese ancestry controls Illumina [at least 870261] (imputed) 16 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST009356 Genome-wide genotyping array 2019-11-08 27894865 Gago-Diaz M 2016-11-25 J Mol Cell Cardiol www.ncbi.nlm.nih.gov/pubmed/27894865 The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study. Bicuspid aortic valve without aortic dilation 565 European ancestry cases, 484 European ancestry controls 895 European ancestry cases, 1,493 European ancestry controls Illumina [up to 82000000] (imputed) 1 Bicuspid aortic valve http://purl.obolibrary.org/obo/HP_0001647 GCST009006 Exome genotyping array [Exome array] 2019-11-08 27894865 Gago-Diaz M 2016-11-25 J Mol Cell Cardiol www.ncbi.nlm.nih.gov/pubmed/27894865 The genetic component of bicuspid aortic valve and aortic dilation. An exome-wide association study. Bicuspid aortic valve 565 European ancestry cases, 484 European ancestry controls 895 European ancestry cases, 1,493 European ancestry controls Illumina [up to 82000000] (imputed) 0 Bicuspid aortic valve http://purl.obolibrary.org/obo/HP_0001647 GCST009005 Exome genotyping array [Exome array] 2018-09-12 29903748 Debiec H 2018-06-14 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29903748 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. Childhood steroid-sensitive nephrotic syndrome 244 European ancestry cases, 2,552 European ancestry controls, 56 African cases, 454 African controls, 85 Maghrebian cases, 261 Maghrebian controls NA Illumina [at least 7529344] (imputed) 5 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST006252 Genome-wide genotyping array 2020-02-28 29903748 Debiec H 2018-06-14 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29903748 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. Childhood steroid-sensitive nephrotic syndrome 132 European ancestry cases, 2,000 European ancestry controls NA Illumina [at least 7529344] (imputed) 2 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST009711 Genome-wide genotyping array 2020-02-28 29903748 Debiec H 2018-06-14 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29903748 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. Childhood steroid-sensitive nephrotic syndrome 56 African cases, 454 African controls NA Illumina [at least 7529344] (imputed) 2 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST009709 Genome-wide genotyping array 2020-02-28 29903748 Debiec H 2018-06-14 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/29903748 Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome. Childhood steroid-sensitive nephrotic syndrome 85 Maghrebian cases, 261 Maghrebian controls NA Illumina [at least 7529344] (imputed) 1 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST009710 Genome-wide genotyping array 2019-10-08 31504236 Wiberg A 2019-09-05 Brain www.ncbi.nlm.nih.gov/pubmed/31504236 Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics. Handedness (non-right-handed vs right-handed) 44,631 European ancestry non-right-handed individuals, 356,567 European ancestry right-handed individuals NA NR [~ 11000000] (imputed) 2 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST008820 Genome-wide genotyping array 2019-10-08 31504236 Wiberg A 2019-09-05 Brain www.ncbi.nlm.nih.gov/pubmed/31504236 Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics. Handedness (Left-handed vs. non-left-handed) 38,322 European ancestry left-handed individuals, 362,866 European ancestry right-handed individuals NA NR [~ 11000000] (imputed) 3 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST008818 Genome-wide genotyping array 2019-10-08 31504236 Wiberg A 2019-09-05 Brain www.ncbi.nlm.nih.gov/pubmed/31504236 Handedness, language areas and neuropsychiatric diseases: insights from brain imaging and genetics. Handedness (left-handed vs. right-handed) 38,322 European ancestry left-handed individuals, 356,567 European ancestry right-handed individuals NA NR [~ 11000000] (imputed) 3 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST008819 Genome-wide genotyping array 2019-12-13 31533690 Orlova E 2019-09-18 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/31533690 Pilot GWAS of caries in African-Americans shows genetic heterogeneity. Dental caries (decayed, missing and filled tooth surfaces) 109 African American adults NA Illumina [~ 4900000] (imputed) 11 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST009268 Genome-wide genotyping array 2019-12-13 31533690 Orlova E 2019-09-18 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/31533690 Pilot GWAS of caries in African-Americans shows genetic heterogeneity. Dental caries (decayed, missing and filled teeth) 109 African American adults NA Illumina [~ 4900000] (imputed) 25 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST009267 Genome-wide genotyping array 2019-12-13 31533690 Orlova E 2019-09-18 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/31533690 Pilot GWAS of caries in African-Americans shows genetic heterogeneity. Dental caries (decayed and filled deciduous teeth) 96 African American children NA Illumina [~ 4900000] (imputed) 25 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST009269 Genome-wide genotyping array 2019-12-13 31533690 Orlova E 2019-09-18 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/31533690 Pilot GWAS of caries in African-Americans shows genetic heterogeneity. Dental caries (decayed and filled deciduous tooth surfaces) 96 African American children NA Illumina [~ 4900000] (imputed) 17 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST009266 Genome-wide genotyping array 2019-09-29 31476763 Otsuka I 2019-09-02 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/31476763 Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population. Age at suicide 719 Japanese ancestry individuals NA Illumina [8810873] (imputed) 3 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST008771 Genome-wide genotyping array 2019-09-29 31476763 Otsuka I 2019-09-02 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/31476763 Genome-wide association studies identify polygenic effects for completed suicide in the Japanese population. Suicide 746 Japanese ancestry cases, 14,049 Japanese ancestry controls NA Illumina [8625325] (imputed) 6 suicide http://www.ebi.ac.uk/efo/EFO_0007624 GCST008772 Genome-wide genotyping array 2019-10-01 31511532 Teumer A 2019-09-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31511532 Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Urinary albumin-to-creatinine ratio 547,361 European ancestry individuals NA Affymetrix, Illumina [8603712] (imputed) 63 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST008794 Genome-wide genotyping array 2019-10-01 31511532 Teumer A 2019-09-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31511532 Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Urinary albumin-to-creatinine ratio 6,795 African American individuals NA Affymetrix, Illumina [at least 8034757] (imputed) 1 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST008793 Genome-wide genotyping array 2019-10-01 31511532 Teumer A 2019-09-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31511532 Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Urinary albumin-to-creatinine ratio in diabetes 51,541 European, African American, East Asian, South Asian or Hispanic ancestry individuals NA Affymetrix, Illumina [8034757] (imputed) 8 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST008792 Genome-wide genotyping array 2019-10-01 31511532 Teumer A 2019-09-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31511532 Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Microalbuminuria 51,861 European, African American, East Asian, South Asian or Hispanic ancestry cases, 297,093 European, African American, East Asian, South Asian or Hispanic ancestry controls NA Affymetrix, Illumina [8326000] (imputed) 29 Moderate albuminuria http://purl.obolibrary.org/obo/HP_0012594 GCST008791 Genome-wide genotyping array 2019-10-01 31511532 Teumer A 2019-09-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31511532 Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria. Urinary albumin-to-creatinine ratio 547,361 European ancestry individuals, 6,795 African American individuals, 6,324 East Asian ancestry individuals, 2,335 South Asian ancestry individuals, 1,442 Hispanic individuals NA Affymetrix, Illumina [8034757] (imputed) 59 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST008790 Genome-wide genotyping array 2019-09-23 31501611 Karlsson T 2019-09-09 Nat Med www.ncbi.nlm.nih.gov/pubmed/31501611 Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease. Predicted visceral adipose tissue 163,984 British ancestry men NA Affymetrix [10549349] (imputed) 2 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST008743 Genome-wide genotyping array 2019-09-23 31501611 Karlsson T 2019-09-09 Nat Med www.ncbi.nlm.nih.gov/pubmed/31501611 Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease. Predicted visceral adipose tissue 161,168 British ancestry women NA Affymetrix [10549349] (imputed) 2 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST008742 Genome-wide genotyping array 2019-09-23 31501611 Karlsson T 2019-09-09 Nat Med www.ncbi.nlm.nih.gov/pubmed/31501611 Contribution of genetics to visceral adiposity and its relation to cardiovascular and metabolic disease. Predicted visceral adipose tissue 325,153 British ancestry individuals NA Affymetrix [10549349] (imputed) 205 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST008744 Genome-wide genotyping array 2019-11-26 31545351 Irvin MR 2019-09-23 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/31545351 Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group. Resistant hypertension 931 European ancestry cases, 228 African American ancestry cases, 14,210 European ancestry controls, 2,480 African American ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST009098 Genome-wide genotyping array 2019-11-26 31545351 Irvin MR 2019-09-23 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/31545351 Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group. Resistance to antihypertensive treatment in hypertension 931 European ancestry cases, 228 African American ancestry cases, 5,266 European ancestry controls, 1,817 African American ancestry controls NA Affymetrix, Illumina [NR] (imputed) 4 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST009103 Genome-wide genotyping array 2019-11-26 31545351 Irvin MR 2019-09-23 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/31545351 Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group. Resistant hypertension 931 European ancestry cases, 14,210 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 2 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST009102 Genome-wide genotyping array 2019-11-26 31545351 Irvin MR 2019-09-23 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/31545351 Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group. Resistance to antihypertensive treatment in hypertension 931 European ancestry cases, 14,210 European ancestry controls 11,762 European ancestry cases, 42,850 European ancestry controls Affymetrix, Illumina [NR] (imputed) 1 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST009101 Genome-wide genotyping array 2019-11-26 31545351 Irvin MR 2019-09-23 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/31545351 Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group. Resistant hypertension 228 African American ancestry cases, 2,480 African American ancestry controls NA Affymetrix, Illumina [NR] (imputed) 4 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST009100 Genome-wide genotyping array 2019-11-26 31545351 Irvin MR 2019-09-23 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/31545351 Genome wide association study of apparent treatment resistant hypertension in the CHARGE consortium: The CHARGE Pharmacogenetics Working Group. Resistance to antihypertensive treatment in hypertension 228 African American ancestry cases, 2,480 African American ancestry controls 5,071 African American ancestry cases, 11,081 African American ancestry controls Affymetrix, Illumina [NR] (imputed) 0 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST009099 Genome-wide genotyping array 2019-10-08 31319653 Jeon C 2019-07-12 Epidemiol Health www.ncbi.nlm.nih.gov/pubmed/31319653 Bilirubin and risk of ischemic heart disease in Korea: A two-sample Mendelian randomization study. Ischemic heart disease 1,910 Korean ancestry cases, 11,945 Korean ancestry controls NA NR [at least 830000] (imputed) 0 Myocardial Ischemia http://www.ebi.ac.uk/efo/EFO_1001375 GCST008816 Genome-wide genotyping array 2019-10-08 31319653 Jeon C 2019-07-12 Epidemiol Health www.ncbi.nlm.nih.gov/pubmed/31319653 Bilirubin and risk of ischemic heart disease in Korea: A two-sample Mendelian randomization study. Bilirubin levels 33,598 Korean ancestry individuals NA NR [at least 830000] (imputed) 5 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST008817 Genome-wide genotyping array 2019-12-02 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Height 347,086 European ancestry individuals NA NR [5554549] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST009142 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. BMI-adjusted waist-hip ratio variance 346,535 European ancestry individuals NA NR [5554549] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST009127 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Body fat percentage variance 341,632 European ancestry individuals NA NR [5554549] (imputed) 5 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST009105 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Basal metabolic rate variance 341,584 European ancestry individuals NA NR [5554549] (imputed) 5 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST009106 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Body mass index variance 346,393 European ancestry individuals NA NR [5554549] (imputed) 22 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009107 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Waist circumference variance 347,158 European ancestry individuals NA NR [5554549] (imputed) 16 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST009108 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Hip circumference variance 346,781 European ancestry individuals NA NR [5554549] (imputed) 16 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST009109 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Waist-hip ratio variance 347,134 European ancestry individuals NA NR [5554549] (imputed) 1 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST009110 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Height variance 347,086 European ancestry individuals NA NR [5554549] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST009111 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Lung function (forced vital capacity) variance 317,222 European ancestry individuals NA NR [5554549] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST009112 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Lung function (FEV1) variance 317,285 European ancestry individuals NA NR [5554549] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST009113 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Lung function (FEV1/FVC) variance 316,614 European ancestry individuals NA NR [5554549] (imputed) 3 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST009114 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Heel bone mineral density variance 197,261 European ancestry individuals NA NR [5554549] (imputed) 6 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST009115 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Birth weight variance 197,758 European ancestry individuals NA NR [5554549] (imputed) 1 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST009116 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Lung function (forced vital capacity) 317,222 European ancestry individuals NA NR [5554549] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST009117 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Lung function (FEV1) 317,285 European ancestry individuals NA NR [5554549] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST009118 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Lung function (FEV1/FVC) 316,614 European ancestry individuals NA NR [5554549] (imputed) 3 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST009119 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Heel bone mineral density 197,261 European ancestry individuals NA NR [5554549] (imputed) 6 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST009120 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Birth weight 197,758 European ancestry individuals NA NR [5554549] (imputed) 1 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST009128 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Body mass index 346,393 European ancestry individuals NA NR [5554549] (imputed) 22 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009121 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Waist circumference 347,158 European ancestry individuals NA NR [5554549] (imputed) 13 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST009122 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Hip circumference 346,781 European ancestry individuals NA NR [5554549] (imputed) 16 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST009123 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Waist-hip ratio 347,134 European ancestry individuals NA NR [5554549] (imputed) 1 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST009124 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Waist-to-hip ratio adjusted for BMI 346,535 European ancestry individuals NA NR [5554549] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST009125 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Body fat percentage 341,632 European ancestry individuals NA NR [5554549] (imputed) 3 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST009126 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Blood pressure 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 2 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST008964 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Glucose homeostasis traits 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 6 diabetes mellitus biomarker http://www.ebi.ac.uk/efo/EFO_0006842 GCST008963 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Hematology traits 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 15 hematological measurement http://www.ebi.ac.uk/efo/EFO_0004503 GCST008962 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Hormone measurements 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 7 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST008957 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. C-reactive protein levels 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST008961 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Iron status biomarkers 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 1 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST008960 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Lipid traits 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 14 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST008959 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Liver disease biomarker 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 2 liver disease biomarker http://www.ebi.ac.uk/efo/EFO_0006845 GCST008965 Genome-wide genotyping array 2019-10-28 30576415 Gilly A 2019-08-01 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/30576415 Very low-depth whole-genome sequencing in complex trait association studies. Anthropometric traits 1,225 Mylopotamos (founder/genetic isolate) individuals NA Illumina [14948665] (imputed) 5 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST008958 Genome-wide genotyping array 2019-10-23 31579629 Fiorica PN 2019-09-26 PeerJ www.ncbi.nlm.nih.gov/pubmed/31579629 Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia. Bipolar disorder 671 African American cases, 348 African American controls NA Affymetrix [12799548] (imputed) 1 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST008905 Genome-wide genotyping array 2019-10-23 31579629 Fiorica PN 2019-09-26 PeerJ www.ncbi.nlm.nih.gov/pubmed/31579629 Transcriptome association studies of neuropsychiatric traits in African Americans implicate PRMT7 in schizophrenia. Schizophrenia 969 African American cases, 1,287 African American controls NA Affymetrix [12780487] (imputed) 2 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST008906 Genome-wide genotyping array 2019-11-27 31453325 Wang H 2019-08-14 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31453325 Genotype-by-environment interactions inferred from genetic effects on phenotypic variability in the UK Biobank. Basal metabolic rate 341,584 European ancestry individuals NA NR [5554549] (imputed) 5 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST009129 Genome-wide genotyping array 2020-01-27 31667592 Milet J 2019-10-30 Hum Genet www.ncbi.nlm.nih.gov/pubmed/31667592 First genome-wide association study of non-severe malaria in two birth cohorts in Benin. Recurrence of malaria infection (mild or asymptomatic) 525 Beninese individuals 250 Beninese individuals Illumina [15566900] (imputed) 2 disease recurrence, malaria http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0001068 GCST009515 Genome-wide genotyping array 2020-01-27 31667592 Milet J 2019-10-30 Hum Genet www.ncbi.nlm.nih.gov/pubmed/31667592 First genome-wide association study of non-severe malaria in two birth cohorts in Benin. Recurrence of mild malaria attacks 525 Beninese individuals 250 Beninese individuals Illumina [15566900] (imputed) 6 disease recurrence, malaria http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0001068 GCST009514 Genome-wide genotyping array 2020-01-09 31591132 Wu W 2019-10-07 Genetics www.ncbi.nlm.nih.gov/pubmed/31591132 Retrospective Association Analysis of Longitudinal Binary Traits Identifies Important Loci and Pathways in Cocaine Use. Longitudinal cocaine use 1,682 mostly never users, 296 moderate decrease users, 86 elevated chronic users, 167 mostly frequent users NA Illumina [10215072] (imputed) 12 cocaine use measurement http://www.ebi.ac.uk/efo/EFO_0010553 GCST009384 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Diabetic nephropathy in type 1 diabetes 4,948 European ancestry cases, 12,076 European ancestry controls NA Illumina [up to 49000000] (imputed) 2 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST009278 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Macroalbuminuria in type 1 diabetes 2,751 European ancestry cases, 12,124 European ancestry controls NA Illumina [up to 49000000] (imputed) 2 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST009284 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. End-stage renal disease in Type 1 diabetics 2,187 European ancestry cases, 12,101 European ancestry controls NA Illumina [up to 49000000] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST009279 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Kidney disease (end stage renal disease vs non-end stage renal disease) in type 1 diabetes 2,187 European ancestry cases, 17,219 European ancestry controls NA Illumina [up to 49000000] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST009280 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Kidney disease (end stage renal disease vs macroalbuminuria) in type 1 diabetes 2,187 European ancestry cases, 2,725 European ancestry controls NA Illumina [up to 49000000] (imputed) 1 albuminuria, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0004285, http://www.ebi.ac.uk/efo/EFO_0000401 GCST009285 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Microalbuminuria in type 1 diabetes 2,447 European ancestry cases, 12,113 European ancestry controls NA Illumina [up to 49000000] (imputed) 7 Moderate albuminuria http://purl.obolibrary.org/obo/HP_0012594 GCST009281 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Chronic kidney disease (reduced eGFR or end stage renal disease) in type 1 diabetes 4,266 European ancestry cases, 14,838 European ancestry controls NA Illumina [up to 49000000] (imputed) 2 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST009286 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Chronic kidney disease (end stage renal disease vs. normal eGFR) in type 1 diabetes 2,235 European ancestry cases, 14,993 European ancestry controls NA Illumina [up to 49000000] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST009287 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in type 1 diabetes 2,987 European ancestry cases, 11,766 European ancestry controls NA Illumina [up to 49000000] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST009289 Genome-wide genotyping array 2019-12-16 31537649 Salem RM 2019-09-19 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/31537649 Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen. Kidney disease (end stage renal disease or albuminuria) in type 1 diabetes 7,247 European ancestry cases, 12,053 European ancestry controls NA Illumina [up to 49000000] (imputed) 1 albuminuria, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0004285, http://www.ebi.ac.uk/efo/EFO_0000401 GCST009292 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 760 Central American ancestry individuals up to 8,527 European ancestry individuals, 2,362 African American individuals, 1,447 Hispanic/Latino individuals Illumina [27887661] (imputed) 1 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009139 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 1,500 Cuban ancestry individuals NA Illumina [27887661] (imputed) 1 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009137 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 2,619 Mexican ancestry individuals NA Illumina [27887661] (imputed) 0 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009138 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 700 Dominican ancestry individuals up to 8,527 European ancestry individuals, 2,362 African American individuals, 1,447 Hispanic/Latino individuals Illumina [27887661] (imputed) 1 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009135 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 553 South American ancestry individuals NA Illumina [27887661] (imputed) 0 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009140 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 1,437 Puerto Rican ancestry individuals up to 8,527 European ancestry individuals, 2,362 African American individuals, 1,447 Hispanic/Latino individuals Illumina [27887661] (imputed) 2 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009136 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 3,637 Caribbean ancestry individuals up to 8,527 European ancestry individuals, 2,362 African American individuals, 1,447 Hispanic/Latino individuals Illumina [27887661] (imputed) 1 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009141 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Peripheral artery disease 382 Hispanic/Latino cases, 7,015 Hispanic/Latino controls NA Illumina [27887661] (imputed) 0 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST009133 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Peripheral artery disease (borderline) 2,104 Hispanic/Latino cases, 5,293 Hispanic/Latino controls NA Illumina [27887661] (imputed) 1 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST009134 Genome-wide genotyping array 2019-11-29 31388106 Sofer T 2019-08-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31388106 Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. Ankle-brachial index 7,589 Hispanic/Latino individuals NA Illumina [27887661] (imputed) 0 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST009132 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (total) 866 European and unknown ancestry individuals NA Illumina [> 2600000] (imputed) 3 chromosomal aberration frequency http://www.ebi.ac.uk/efo/EFO_0009860 GCST008940 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (chromatid type) 333 European and unknown ancestry cases, 533 European and unknown ancestry controls NA Illumina [> 2600000] (imputed) 2 chromatid-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009862 GCST008941 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (chromatid type) 866 European and unknown ancestry individuals NA Illumina [> 2600000] (imputed) 4 chromatid-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009862 GCST008942 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (chromosome type) 333 European and unknown ancestry cases, 533 European and unknown ancestry controls NA Illumina [> 2600000] (imputed) 2 chromosome-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009861 GCST008943 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (chromosome type) 866 European and unknown ancestry individuals NA Illumina [> 2600000] (imputed) 4 chromosome-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009861 GCST008944 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (total) in genotoxic compound exposure 342 European and unknown ancestry cases, 265 European and unknown ancestry controls NA Illumina [> 2600000] (imputed) 0 chromosomal aberration frequency http://www.ebi.ac.uk/efo/EFO_0009860 GCST008945 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (total) in genotoxic compound exposure 607 European and unknown ancestry individuals NA Illumina [> 2600000] (imputed) 1 chromosomal aberration frequency http://www.ebi.ac.uk/efo/EFO_0009860 GCST008946 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (chromatid type) in genotoxic compound exposure 345 European and unknown ancestry cases, 262 European and unknown ancestry controls NA Illumina [> 2600000] (imputed) 2 chromatid-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009862 GCST008947 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (chromatid type) in genotoxic compound exposure 607 European and unknown ancestry individuals NA Illumina [> 2600000] (imputed) 4 chromatid-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009862 GCST008948 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (chromosome type) in genotoxic compound exposure 321 European and unknown ancestry cases, 286 European and unknown ancestry controls NA Illumina [> 2600000] (imputed) 2 chromosome-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009861 GCST008949 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (chromosome type) in genotoxic compound exposure 607 European and unknown ancestry individuals NA Illumina [> 2600000] (imputed) 2 chromosome-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009861 GCST008939 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (total) 342 European and unknown ancestry genotoxic compound-exposed cases, 265 European and unknown ancestry genotoxic compound-exposed controls,255 European and unknown ancestry unexposed cases, 611 European and unknown ancestry unexposed controls NA Illumina [> 2600000] (imputed) 3 chromosomal aberration frequency http://www.ebi.ac.uk/efo/EFO_0009860 GCST008950 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (total) 607 European and unknown ancestry genotoxic compound-exposed individuals, 866 European and unknown ancestry unexposed individuals NA Illumina [> 2600000] (imputed) 2 chromosomal aberration frequency http://www.ebi.ac.uk/efo/EFO_0009860 GCST008951 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (chromatid type) 345 European and unknown ancestry genotoxic compound-exposed cases, 262 European and unknown ancestry genotoxic compound-exposed controls, 333 European and unknown ancestry unexposed cases, 533 European and unknown ancestry unexposed controls NA Illumina [> 2600000] (imputed) 3 chromatid-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009862 GCST008952 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (chromatid type) 607 European and unknown ancestry genotoxic compound-exposed individuals, 866 European and unknown ancestry unexposed individuals NA Illumina [> 2600000] (imputed) 3 chromatid-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009862 GCST008953 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (chromosome type) 321 European and unknown ancestry genotoxic compound-exposed cases, 286 European and unknown ancestry genotoxic compound-exposed controls, 333 European and unknown ancestry unexposed cases, 533 European and unknown ancestry unexposed controls NA Illumina [> 2600000] (imputed) 4 chromosome-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009861 GCST008954 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Chromosomal aberration frequency (chromosome type) 607 European and unknown ancestry genotoxic compound-exposed individuals, 866 European and unknown ancestry unexposed individuals NA Illumina [> 2600000] (imputed) 3 chromosome-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009861 GCST008955 Genome-wide genotyping array 2019-10-25 31586183 Niazi Y 2019-10-04 Mutagenesis www.ncbi.nlm.nih.gov/pubmed/31586183 Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. High chromosomal aberration frequency (total) 255 European and unknown ancestry cases, 611 European and unknown ancestry controls NA Illumina [> 2600000] (imputed) 3 chromosomal aberration frequency http://www.ebi.ac.uk/efo/EFO_0009860 GCST008956 Genome-wide genotyping array 2019-11-04 31615970 Rodas G 2019-10-14 Int J Sports Physiol Perform www.ncbi.nlm.nih.gov/pubmed/31615970 Genomic Prediction of Tendinopathy Risk in Elite Team Sports. Tendinopathy 181 European ancestry cases, 12 African American cases, 5 Brazilian cases, 1 Asian ancestry cases, 147 European ancestry controls, 9 African American controls, 7 Brazilian controls, 2 Asian ancestry controls NA Illumina [1419369] (imputed) 2 Tendinopathy http://www.ebi.ac.uk/efo/EFO_1001434 GCST009002 Genome-wide genotyping array 2019-09-24 31296530 Trendowski MR 2019-07-11 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/31296530 Clinical and Genome-Wide Analysis of Serum Platinum Levels after Cisplatin-Based Chemotherapy. Serum platinum levels after completion of cisplatin chemotherapy 866 European ancestry individuals, 17 non-European ancestry individuals, 127 individuals NR Illumina [7305641] (imputed) 33 response to cisplatin, platinum measurement http://purl.obolibrary.org/obo/GO_0072718, http://www.ebi.ac.uk/efo/EFO_0010154 GCST008756 Genome-wide genotyping array 2019-08-01 31246245 Khawaja AP 2019-06-27 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31246245 Genetic Variants Associated With Corneal Biomechanical Properties and Potentially Conferring Susceptibility to Keratoconus in a Genome-Wide Association Study. Corneal resistance factor 6,645 individuals 2,384 European ancestry individuals Affymetrix [NR] (imputed) 8 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST008276 Genome-wide genotyping array 2019-08-01 31246245 Khawaja AP 2019-06-27 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31246245 Genetic Variants Associated With Corneal Biomechanical Properties and Potentially Conferring Susceptibility to Keratoconus in a Genome-Wide Association Study. Corneal hysteresis 6,645 individuals 2,384 European ancestry individuals Affymetrix [NR] (imputed) 5 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST008277 Genome-wide genotyping array 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. Total cholesterol levels up to 237,050 European ancestry individuals, up to 16,935 African ancestry individuals, up to 30,468 South Asian ancestry individuals, up to 8,287 East Asian ancestry individuals, 5,084 Hispanic individuals up to 286,268 European and unknown ancestry individuals Illumina [242289] 15 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST009145 Exome genotyping array [Exome array] 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. Total cholesterol levels up to 237,050 European ancestry individuals NA Illumina [242289] 16 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST009146 Exome genotyping array [Exome array] 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. Low density lipoprotein cholesterol levels up to 237,050 European ancestry individuals NA Illumina [242289] 19 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST009147 Exome genotyping array [Exome array] 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. High density lipoprotein cholesterol levels up to 237,050 European ancestry individuals NA Illumina [242289] 23 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009148 Exome genotyping array [Exome array] 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. Triglyceride levels up to 237,050 European ancestry individuals NA Illumina [242289] 18 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST009149 Exome genotyping array [Exome array] 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. Low density lipoprotein cholesterol levels up to 237,050 European ancestry individuals, up to 16,935 African ancestry individuals, up to 30,468 South Asian ancestry individuals, up to 8,287 East Asian ancestry individuals, 5,084 Hispanic individuals up to 286,268 European and unknown ancestry individuals Illumina [242289] 17 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST009150 Exome genotyping array [Exome array] 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. High density lipoprotein cholesterol levels up to 237,050 European ancestry individuals, up to 16,935 African ancestry individuals, up to 30,468 South Asian ancestry individuals, up to 8,287 East Asian ancestry individuals, 5,084 Hispanic individuals up to 286,268 European and unknown ancestry individuals Illumina [242289] 24 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009151 Exome genotyping array [Exome array] 2019-12-03 29083408 Liu DJ 2017-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29083408 Exome-wide association study of plasma lipids in >300,000 individuals. Triglyceride levels up to 237,050 European ancestry individuals, up to 16,935 African ancestry individuals, up to 30,468 South Asian ancestry individuals, up to 8,287 East Asian ancestry individuals, 5,084 Hispanic individuals up to 286,268 European and unknown ancestry individuals Illumina [242289] 17 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST009152 Exome genotyping array [Exome array] 2020-02-06 31711042 Li X 2019-11-11 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/31711042 Genome-wide association study identifies SIAH3 locus influencing the rate of ventricular enlargement in non-demented elders. Rate of ventricular enlargement 507 European ancestry individuals NA Illumina [1231747] 13 ventricular enlargement measurement http://www.ebi.ac.uk/efo/EFO_0010570 GCST009557 Genome-wide genotyping array 2019-02-28 30541042 Walsh N 2018-12-12 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/30541042 Agnostic Pathway/Gene Set Analysis of Genome-Wide Association Data Identifies Associations for Pancreatic Cancer. Pancreatic ductal adenocarcinoma 9,040 European ancestry cases, 12,496 European ancestry controls NA NR [NR] 9 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST007235 Genome-wide genotyping array 2020-01-27 31339356 Hobbs BD 2019-07-24 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/31339356 Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. Subpleural-predominant interstitial lung abnormalities 965 European ancestry cases, 154 African American cases, 168 cases, 7,255 European ancestry controls, 1,717 African American controls, 450 controls NA Affymetrix, Illumina [at least 412049] (imputed) 6 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST009502 Genome-wide genotyping array 2020-01-27 31339356 Hobbs BD 2019-07-24 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/31339356 Overlap of Genetic Risk Between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis. Interstitial lung abnormalities 1,181 European ancestry cases, 280 African American cases, 54 Hispanic cases, 184 cases, 7,255 European ancestry controls, 2,184 African American controls, 385 Hispanic controls, 450 controls NA Affymetrix, Illumina [at least 412049] (imputed) 7 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST009501 Genome-wide genotyping array 2020-01-20 31887566 Carrion-Castillo A 2019-11-29 Cortex www.ncbi.nlm.nih.gov/pubmed/31887566 Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment. Left planum temporale grey matter volume 18,037 British ancestry individuals NA Affymetrix [15120452] (imputed) 1 superior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010331 GCST009460 Genome-wide genotyping array 2020-01-20 31887566 Carrion-Castillo A 2019-11-29 Cortex www.ncbi.nlm.nih.gov/pubmed/31887566 Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment. Right planum temporale grey matter volume 18,039 British ancestry individuals NA Affymetrix [15120452] (imputed) 1 superior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010331 GCST009458 Genome-wide genotyping array 2020-01-20 31887566 Carrion-Castillo A 2019-11-29 Cortex www.ncbi.nlm.nih.gov/pubmed/31887566 Genetic effects on planum temporale asymmetry and their limited relevance to neurodevelopmental disorders, intelligence or educational attainment. Planum temporale asymmetry index 18,049 British ancestry individuals NA Affymetrix [15120452] (imputed) 2 superior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010331 GCST009459 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Chronic lymphocytic leukemia or multiple sclerosis 2,492 European ancestry chronic lymphocytic leukemia cases, 9,772 European ancestry multiple sclerosis cases, 24,529 European ancestry controls NA Illumina [~ 460000] (imputed) 7 multiple sclerosis, chronic lymphocytic leukemia http://purl.obolibrary.org/obo/MONDO_0005301, http://www.ebi.ac.uk/efo/EFO_0000095 GCST008721 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Diffuse large B-cell lymphoma or multiple sclerosis 3,617 European ancestry diffuse large B-cell lymphoma cases, 9,772 European ancestry multiple sclerosis cases, 24,813 European ancestry controls NA Illumina [~ 460000] (imputed) 5 diffuse large B-cell lymphoma, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0000403, http://purl.obolibrary.org/obo/MONDO_0005301 GCST008722 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Follicular lymphoma or multiple sclerosis 2,686 European ancestry follicular lymphoma cases, 9,772 European ancestry multiple sclerosis cases, 25,256 European ancestry controls NA Illumina [~ 460000] (imputed) 2 follicular lymphoma, multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0018906, http://purl.obolibrary.org/obo/MONDO_0005301 GCST008718 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Marginal zone lymphoma or multiple sclerosis 741 European ancestry marginal zone lymphoma cases, 9,772 European ancestry multiple sclerosis cases, 23,367 European ancestry controls NA Illumina [~ 460000] (imputed) 7 marginal zone B-cell lymphoma, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_1000630, http://purl.obolibrary.org/obo/MONDO_0005301 GCST008723 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Chronic lymphocytic leukemia or rheumatoid arthritis 2,492 European ancestry chronic lymphocytic leukemia cases, 3,921 European ancestry rheumatoid arthritis cases, 11,232 European ancestry controls NA Illumina [~ 600000] (imputed) 1 rheumatoid arthritis, chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0000095 GCST008724 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Diffuse large B-cell lymphoma or rheumatoid arthritis 3,617 European ancestry diffuse large B-cell lymphoma cases, 3,921 European ancestry rheumatoid arthritis cases, 11,516 European ancestry controls NA Illumina [~ 600000] (imputed) 1 diffuse large B-cell lymphoma, rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000403, http://www.ebi.ac.uk/efo/EFO_0000685 GCST008725 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Follicular lymphoma or rheumatoid arthritis 2,686 European ancestry follicular lymphoma cases, 3,921 European ancestry rheumatoid arthritis cases, 11,959 European ancestry controls NA Illumina [~ 600000] (imputed) 1 rheumatoid arthritis, follicular lymphoma http://www.ebi.ac.uk/efo/EFO_0000685, http://purl.obolibrary.org/obo/MONDO_0018906 GCST008719 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Marginal zone lymphoma or rheumatoid arthritis 741 European ancestry marginal zone lymphoma cases, 3,921 European ancestry rheumatoid arthritis cases, 10,070 European ancestry controls NA Illumina [~ 600000] (imputed) 2 rheumatoid arthritis, marginal zone B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_1000630 GCST008726 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Chronic lymphocytic leukemia or systemic lupus erythematosus 2,492 European ancestry chronic lymphocytic leukemia cases, 7,219 European ancestry systemic lupus erythematosus cases, 23,144 European ancestry controls NA Illumina [~ 600000] (imputed) 4 systemic lupus erythematosus, chronic lymphocytic leukemia http://purl.obolibrary.org/obo/MONDO_0007915, http://www.ebi.ac.uk/efo/EFO_0000095 GCST008727 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Diffuse large B-cell lymphoma or systemic lupus erythematosus 3,617 European ancestry diffuse large B-cell lymphoma cases, 7,219 European ancestry systemic lupus erythematosus cases, 23,428 European ancestry controls NA Illumina [~ 600000] (imputed) 1 diffuse large B-cell lymphoma, systemic lupus erythematosus http://www.ebi.ac.uk/efo/EFO_0000403, http://purl.obolibrary.org/obo/MONDO_0007915 GCST008728 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Follicular lymphoma or systemic lupus erythematosus 2,686 European ancestry follicular lymphoma cases, 7,219 European ancestry systemic lupus erythematosus cases, 23,871 European ancestry controls NA Illumina [~ 600000] (imputed) 0 systemic lupus erythematosus, follicular lymphoma http://purl.obolibrary.org/obo/MONDO_0007915, http://purl.obolibrary.org/obo/MONDO_0018906 GCST008720 Genome-wide genotyping array 2019-09-20 31407831 Din L 2019-08-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31407831 Genetic overlap between autoimmune diseases and non-Hodgkin lymphoma subtypes. Marginal zone lymphoma or systemic lupus erythematosus 741 European ancestry marginal zone lymphoma cases, 7,219 European ancestry systemic lupus erythematosus cases, 21,982 European ancestry controls NA Illumina [~ 600000] (imputed) 4 marginal zone B-cell lymphoma, systemic lupus erythematosus http://www.ebi.ac.uk/efo/EFO_1000630, http://purl.obolibrary.org/obo/MONDO_0007915 GCST008729 Genome-wide genotyping array 2019-09-20 31413141 Deming Y 2019-08-01 Sci Transl Med www.ncbi.nlm.nih.gov/pubmed/31413141 The MS4A gene cluster is a key modulator of soluble TREM2 and Alzheimer's disease risk. Cerebrospinal fluid sTREM-2 levels 813 individuals 580 individuals Illumina [7320475] (imputed) 2 soluble triggering receptor expressed on myeloid cells 2 measurement http://www.ebi.ac.uk/efo/EFO_0010151 GCST008706 Genome-wide genotyping array 2019-09-23 31466081 Luo A 2019-08-29 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/31466081 Epigenetic aging is accelerated in alcohol use disorder and regulated by genetic variation in APOL2. Epigenetic age acceleration in alcohol use disorder 154 European ancestry individuals, 156 African American individuals NA Illumina [up to 666531] 11 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST008748 Genome-wide genotyping array 2020-02-12 31589552 Lind L 2019-10-07 Metab Syndr Relat Disord www.ncbi.nlm.nih.gov/pubmed/31589552 Genome-Wide Association Study of the Metabolic Syndrome in UK Biobank. Metabolic syndrome 291,107 European ancestry individuals NA Affymetrix [9463307] (imputed) 93 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST009602 Genome-wide genotyping array 2020-01-08 31597885 Nakano MH 2019-10-09 Biol Pharm Bull www.ncbi.nlm.nih.gov/pubmed/31597885 A Genome-Wide Association Study Identifies Five Novel Genetic Markers for Trastuzumab-Induced Cardiotoxicity in Japanese Population. Trastuzumab-induced cardiotoxicity in cancer 11 Japanese ancestry cases, 257 Japanese ancestry controls 14 Japanese ancestry cases, 199 Japanese ancestry controls Illumina [543807] 1 response to trastuzumab, cardiotoxicity http://www.ebi.ac.uk/efo/EFO_0008347, http://www.ebi.ac.uk/efo/EFO_1001482 GCST009381 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Abstraction and mental flexibility 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 19 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST009303 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Emotional recognition 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA NR [> 6200000] (imputed) 9 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST009308 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Face memory 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 13 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST009309 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Sensorimotor dexterity 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 35 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST009310 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Spatial memory 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 20 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST009307 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Spatial processing 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 23 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST009306 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. California verbal learning test score 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 17 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST009305 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Degraded stimulus continuous performance test score 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 16 attention function measurement http://www.ebi.ac.uk/efo/EFO_0007636 GCST009304 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Letter-number span reordering 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 9 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST009311 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Prepulse inhibition of the startle response 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 10 cognitive inhibition measurement http://www.ebi.ac.uk/efo/EFO_0007969 GCST009313 Genome-wide genotyping array 2019-12-17 31596458 Greenwood TA 2019-10-09 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31596458 Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study. Antisaccade task score 523 European ancestry schizophrenia cases, 100 Latino schizophrenia cases, 827 European ancestry controls, 83 Latino controls NA Illumina [> 6200000] (imputed) 24 cognitive inhibition measurement http://www.ebi.ac.uk/efo/EFO_0007969 GCST009312 Genome-wide genotyping array 2019-08-22 26635082 Soler Artigas M 2015-12-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26635082 Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Lung function (FVC) 38,199 European ancestry adults 54,550 European ancestry adults, 5,062 children Affymetrix, Illumina [8694268] (imputed) 10 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST008482 Genome-wide genotyping array 2019-08-22 26635082 Soler Artigas M 2015-12-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26635082 Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Lung function (FEV1/FVC) 38,199 European ancestry adults 54,550 European ancestry adults, 5,062 children Affymetrix, Illumina [8694268] (imputed) 11 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST008481 Genome-wide genotyping array 2019-08-22 26635082 Soler Artigas M 2015-12-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26635082 Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation. Lung function (FEV1) 38,199 European ancestry adults 54,550 European ancestry adults, 5,062 children Affymetrix, Illumina [8694268] (imputed) 13 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST008480 Genome-wide genotyping array 2019-12-16 31591465 Bigdeli TB 2019-10-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31591465 Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry. Schizophrenia or schizoaffective disorder 6,152 African ancestry cases, 1,234 Latino cases, 34,241 European and East Asian ancestry cases, 3,918 African ancestry controls, 3,090 Latino controls, 45,604 European and East Asian ancestry controls, 1,235 European ancestry trios NA Illumina [NR] (imputed) 3 schizophrenia, schizoaffective disorder http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0005411 GCST009283 Genome-wide genotyping array 2020-01-13 31537701 Obeidat M 2019-09-19 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31537701 The Pharmacogenomics of Inhaled Corticosteroids and Lung Function Decline in COPD. FEV1 decline rate x corticosteroid treatment interaction in chronic obstructive pulmonary disease 401 European ancestry drug-treated cases, 401 European ancestry placebo-treated cases 163 drug-treated cases, 36 placebo-treated cases Illumina [6559489] (imputed) 0 FEV change measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0031960 GCST009428 Genome-wide genotyping array 2019-08-21 31285632 Klarin D 2019-07-08 Nat Med www.ncbi.nlm.nih.gov/pubmed/31285632 Genome-wide association study of peripheral artery disease in the Million Veteran Program. Peripheral artery disease 24,009 European ancestry cases, 150,983 European ancestry controls, 5,373 African ancestry cases, 42,485 African ancestry controls, 1,925 Hispanic cases, 18,285 Hispanic controls 5,117 European ancestry cases, 389,291 European ancestry controls Affymetrix [at least 20323458] (imputed) 20 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST008474 Genome-wide genotyping array 2019-08-21 31285632 Klarin D 2019-07-08 Nat Med www.ncbi.nlm.nih.gov/pubmed/31285632 Genome-wide association study of peripheral artery disease in the Million Veteran Program. Minimum ankle–brachial index 13,382 European ancestry individuals, 3,284 African ancestry individuals, 998 Hispanic individuals NA Affymetrix [at least 9211766] (imputed) 2 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST008475 Genome-wide genotyping array 2019-07-16 30924126 Brackman DJ 2019-03-28 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/30924126 Genome-wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol. Response to allopurinol in gout (change in serum uric acid levels) 2,647 European ancestry cases, 303 East Asian cases, 115 African American cases, 114 Latino cases 355 European ancestry cases Affymetrix, Illumina [NR] (imputed) 1 response to allopurinol, uric acid measurement http://www.ebi.ac.uk/efo/EFO_0006337, http://www.ebi.ac.uk/efo/EFO_0004761 GCST008148 Genome-wide genotyping array 2019-07-16 30924126 Brackman DJ 2019-03-28 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/30924126 Genome-wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol. Response to allopurinol in gout (change in serum uric acid levels) 2,647 European ancestry cases, 303 East Asian cases, 115 African American cases, 114 Latino cases 318 European ancestry cases, 502 European ancestry cases Affymetrix, Illumina [NR] (imputed) 1 response to allopurinol, uric acid measurement http://www.ebi.ac.uk/efo/EFO_0006337, http://www.ebi.ac.uk/efo/EFO_0004761 GCST008147 Genome-wide genotyping array 2019-08-01 31209788 Li HQ 2019-06-18 Neurotox Res www.ncbi.nlm.nih.gov/pubmed/31209788 Genome-Wide Association Study of Cerebral Microbleeds on MRI. Cerebral microbleed progression 57 European ancestry cases, 95 European ancestry controls NA Illumina [979539] 1 cerebral microbleeds, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0010059, http://www.ebi.ac.uk/efo/EFO_0008336 GCST008274 Genome-wide genotyping array 2019-08-01 31209788 Li HQ 2019-06-18 Neurotox Res www.ncbi.nlm.nih.gov/pubmed/31209788 Genome-Wide Association Study of Cerebral Microbleeds on MRI. Cerebral microbleeds 176 European ancestry cases, 278 European ancestry controls NA Illumina [983392] 6 cerebral microbleeds http://www.ebi.ac.uk/efo/EFO_0010059 GCST008275 Genome-wide genotyping array 2019-07-30 31295674 Condreay LD 2019-07-05 Respir Med www.ncbi.nlm.nih.gov/pubmed/31295674 No genetic associations with mepolizumab efficacy in COPD with peripheral blood eosinophilia. Exacerbation frequency in mepolizumab-treated chronic obstructive pulmonary disease 504 European ancestry individuals, 73 Asian ancestry individuals, 18 Native American individuals, 5 African American individuals, 10 individuals NA Affymetrix [10000000] (imputed) 0 respiratory symptom measurement, response to mepolizumab http://www.ebi.ac.uk/efo/EFO_0007939, http://www.ebi.ac.uk/efo/EFO_0008459 GCST008269 Genome-wide genotyping array 2019-07-30 31295674 Condreay LD 2019-07-05 Respir Med www.ncbi.nlm.nih.gov/pubmed/31295674 No genetic associations with mepolizumab efficacy in COPD with peripheral blood eosinophilia. Frequency of exacerbations requiring hospitalisation in mepolizumab-treated chronic obstructive pulmonary disease 504 European ancestry individuals, 73 Asian ancestry individuals, 18 Native American individuals, 5 African American individuals, 10 individuals NA Affymetrix [10000000] (imputed) 0 respiratory symptom measurement, response to mepolizumab http://www.ebi.ac.uk/efo/EFO_0007939, http://www.ebi.ac.uk/efo/EFO_0008459 GCST008268 Genome-wide genotyping array 2019-07-19 31194736 Tiensuu H 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194736 Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. Gestational age at birth (child effect) 666 Finnish ancestry infants NA Illumina [6778521] (imputed) 9 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST008176 Genome-wide genotyping array 2019-07-19 31194736 Tiensuu H 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194736 Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. Spontaneous preterm birth (preterm birth) 247 Finnish ancestry infant cases, 419 Finnish ancestry infant controls NA Illumina [6778521] (imputed) 19 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST008177 Genome-wide genotyping array 2019-07-19 31194736 Tiensuu H 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194736 Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. Early spontaneous preterm birth 172 Finnish ancestry infant cases, 419 Finnish ancestry infant controls NA Illumina [6778521] (imputed) 13 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST008178 Genome-wide genotyping array 2019-07-19 31194736 Tiensuu H 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194736 Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. Moderate-to-late spontaneous preterm birth 75 Finnish ancestry infant cases, 419 Finnish ancestry infant controls NA Illumina [6778521] (imputed) 24 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST008179 Genome-wide genotyping array 2019-07-19 31194736 Tiensuu H 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194736 Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. Spontaneous preterm birth with premature rupture of membranes 133 Finnish ancestry infant cases, 419 Finnish ancestry infant controls NA Illumina [6778521] (imputed) 18 preterm premature rupture of the membranes, spontaneous preterm birth http://purl.obolibrary.org/obo/MONDO_0012511, http://www.ebi.ac.uk/efo/EFO_0006917 GCST008180 Genome-wide genotyping array 2019-07-19 31194736 Tiensuu H 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194736 Risk of spontaneous preterm birth and fetal growth associates with fetal SLIT2. Spontaneous preterm birth without premature rupture of membranes 101 Finnish ancestry infant cases, 419 Finnish ancestry infant controls NA Illumina [6778521] (imputed) 22 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST008181 Genome-wide genotyping array 2019-12-16 31447353 Maciukiewicz M 2019-08-22 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/31447353 Genome-wide association study on antipsychotic-induced weight gain in Europeans and African-Americans. Antipsychotic drug-induced weight gain in schizophrenia 144 European ancestry individuals, 57 African American individuals NA Illumina [1819374] (imputed) 18 antipsychotic drug related weight gain http://www.ebi.ac.uk/efo/EFO_0004567 GCST009302 Genome-wide genotyping array 2019-12-16 31447353 Maciukiewicz M 2019-08-22 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/31447353 Genome-wide association study on antipsychotic-induced weight gain in Europeans and African-Americans. Antipsychotic drug-induced weight gain in schizophrenia or autism 269 European ancestry individuals NA Illumina [NR] (imputed) 1 antipsychotic drug related weight gain http://www.ebi.ac.uk/efo/EFO_0004567 GCST009301 Genome-wide genotyping array 2019-09-12 31409800 Pazoki R 2019-08-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31409800 GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits. Urinary sodium excretion 446,237 European ancestry individuals 7,612 African ancestry individuals, 10,095 South Asian ancestry individuals Affymetrix [~ 8800000] (imputed) 50 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST008647 Genome-wide genotyping array 2019-09-12 31409800 Pazoki R 2019-08-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31409800 GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits. Urinary potassium excretion 446,230 European ancestry individuals 7,612 African ancestry individuals, 10,095 South Asian ancestry individuals Affymetrix [~ 8800000] (imputed) 13 potassium measurement http://www.ebi.ac.uk/efo/EFO_0009283 GCST008648 Genome-wide genotyping array 2019-10-16 30955190 Yun S 2019-04-06 Clin Exp Nephrol www.ncbi.nlm.nih.gov/pubmed/30955190 Genetic risk score raises the risk of incidence of chronic kidney disease in Korean general population-based cohort. Estimated glomerular filtration rate reduction (30%) up to 3,617 Korean ancestry individuals NA Affymetrix [up to 1590162] (imputed) 5 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008837 Genome-wide genotyping array 2019-05-08 30955190 Yun S 2019-04-06 Clin Exp Nephrol www.ncbi.nlm.nih.gov/pubmed/30955190 Genetic risk score raises the risk of incidence of chronic kidney disease in Korean general population-based cohort. Incident chronic kidney disease 281 Korean ancestry cases, 3,336 Korean ancestry controls NA Affymetrix [up to 1590162] (imputed) 2 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST007734 Genome-wide genotyping array 2019-08-22 25489960 Yang SK 2015-01-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/25489960 Immunochip analysis identification of 6 additional susceptibility loci for Crohn's disease in Koreans. Crohn's disease 722 Korean ancestry cases, 461 Korean ancestry controls 948 Korean ancestry cases, 977 Korean ancestry controls Illumina [549616] (imputed) 6 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST008485 Targeted genotyping array [ImmunoChip] 2019-08-29 31260374 Pedergnana V 2019-07-01 J Interferon Cytokine Res www.ncbi.nlm.nih.gov/pubmed/31260374 Impact of IFNL4 Genetic Variants on Sustained Virologic Response and Viremia in Hepatitis C Virus Genotype 3 Patients. Response to interferon treatment in hepatitis C virus genotype 3 717 European, Asian and unknown ancestry responders, 541 European, Asian and unknown ancestry non-responders NA Affymetrix [~ 18000000] (imputed) 8 response to interferon http://www.ebi.ac.uk/efo/EFO_0007859 GCST008517 Genome-wide genotyping array 2019-08-29 31260374 Pedergnana V 2019-07-01 J Interferon Cytokine Res www.ncbi.nlm.nih.gov/pubmed/31260374 Impact of IFNL4 Genetic Variants on Sustained Virologic Response and Viremia in Hepatitis C Virus Genotype 3 Patients. Response to direct-acting antiviral treatment in hepatitis C virus genotype 3 325 European, Asian and unknown ancestry responders, 84 European, Asian and unknown ancestry non-responders NA Affymetrix [~ 18000000] (imputed) 10 response to antiviral drug http://www.ebi.ac.uk/efo/EFO_0010123 GCST008520 Genome-wide genotyping array 2019-08-29 31260374 Pedergnana V 2019-07-01 J Interferon Cytokine Res www.ncbi.nlm.nih.gov/pubmed/31260374 Impact of IFNL4 Genetic Variants on Sustained Virologic Response and Viremia in Hepatitis C Virus Genotype 3 Patients. Pre-treatment viral load in hepatitis C virus genotype 3 1,498 European, Asian and unknown ancestry individuals NA Affymetrix [~ 18000000] (imputed) 1 viral load http://www.ebi.ac.uk/efo/EFO_0010125 GCST008515 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. HDL cholesterol levels 89,893 European ancestry individuals, 20,989 African American individuals, 12,450 Asian ancestry individuals, 3,994 HIspanic individuals 136,986 European ancestry individuals, 4,475 African American or Afro-Caribbean individuals, 108,431 Asian ancestry individuals, 13,714 Hispanic individuals, 3,652 Brazilian ancestry individuals Affymetrix, Illumina [NR] (imputed) 141 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008070 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. LDL cholesterol levels in current drinkers 56,505 European ancestry individuals, 9,870 African American individuals, 2,491 Asian ancestry individuals, 2,528 Hispanic individuals 107,548 European ancestry individuals, 2,028 African American or Afro-Caribbean individuals, 41,240 Asian ancestry individuals, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals Affymetrix, Illumina [NR] (imputed) 118 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008086 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. HDL cholesterol levels in current drinkers 56,505 European ancestry individuals, 9,870 African American individuals, 2,491 Asian ancestry individuals, 2,528 Hispanic individuals 107,548 European ancestry individuals, 2,028 African American or Afro-Caribbean individuals, 41,240 Asian ancestry individuals, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals Affymetrix, Illumina [NR] (imputed) 190 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008085 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Triglyceride levels in current drinkers 56,505 European ancestry individuals, 9,870 African American individuals, 2,491 Asian ancestry individuals, 2,528 Hispanic individuals 107,548 European ancestry individuals, 2,028 African American or Afro-Caribbean individuals, 41,240 Asian ancestry individuals, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals Affymetrix, Illumina [NR] (imputed) 138 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008087 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) 56,505 European ancestry current drinkers, 9,870 African American current drinkers, 2,491 Asian ancestry current drinkers, 2,528 Hispanic current drinkers, 33,388 European ancestry non-drinkers, 11,119 African American non-drinkers, 9,959 Asian ancestry non-drinkers, 1,466 Hispanic non-drinkers 107,548 European ancestry current drinkers, 2,028 African American or Afro-Caribbean current drinkers, 41,240 Asian ancestry current drinkers, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals, 29,438 European ancestry non-drinkers, 2,447 African American or Afro-Caribbean non-drinkers, 67,191 Asian ancestry non-drinkers, 7,092 Hispanic non-drinkers, 1,668 Brazilian ancestry non-drinkers Affymetrix, Illumina [NR] (imputed) 236 alcohol drinking, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004329, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008084 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Triglyceride levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) 56,505 European ancestry current drinkers, 9,870 African American current drinkers, 2,491 Asian ancestry current drinkers, 2,528 Hispanic current drinkers, 33,388 European ancestry non-drinkers, 11,119 African American non-drinkers, 9,959 Asian ancestry non-drinkers, 1,466 Hispanic non-drinkers 107,548 European ancestry current drinkers, 2,028 African American or Afro-Caribbean current drinkers, 41,240 Asian ancestry current drinkers, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals, 29,438 European ancestry non-drinkers, 2,447 African American or Afro-Caribbean non-drinkers, 67,191 Asian ancestry non-drinkers, 7,092 Hispanic non-drinkers, 1,668 Brazilian ancestry non-drinkers Affymetrix, Illumina [NR] (imputed) 162 triglyceride measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004329 GCST008083 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (1df) 56,505 European ancestry current drinkers, 9,870 African American current drinkers, 2,491 Asian ancestry current drinkers, 2,528 Hispanic current drinkers, 33,388 European ancestry non-drinkers, 11,119 African American non-drinkers, 9,959 Asian ancestry non-drinkers, 1,466 Hispanic non-drinkers 107,548 European ancestry current drinkers, 2,028 African American or Afro-Caribbean current drinkers, 41,240 Asian ancestry current drinkers, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals, 29,438 European ancestry non-drinkers, 2,447 African American or Afro-Caribbean non-drinkers, 67,191 Asian ancestry non-drinkers, 7,092 Hispanic non-drinkers, 1,668 Brazilian ancestry non-drinkers Affymetrix, Illumina [NR] (imputed) 0 low density lipoprotein cholesterol measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004329 GCST008082 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. HDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (1df) 56,505 European ancestry current drinkers, 9,870 African American current drinkers, 2,491 Asian ancestry current drinkers, 2,528 Hispanic current drinkers, 33,388 European ancestry non-drinkers, 11,119 African American non-drinkers, 9,959 Asian ancestry non-drinkers, 1,466 Hispanic non-drinkers 107,548 European ancestry current drinkers, 2,028 African American or Afro-Caribbean current drinkers, 41,240 Asian ancestry current drinkers, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals, 29,438 European ancestry non-drinkers, 2,447 African American or Afro-Caribbean non-drinkers, 67,191 Asian ancestry non-drinkers, 7,092 Hispanic non-drinkers, 1,668 Brazilian ancestry non-drinkers Affymetrix, Illumina [NR] (imputed) 0 alcohol drinking, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004329, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008081 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Triglyceride levels x alcohol consumption (drinkers vs non-drinkers) interaction (1df) 56,505 European ancestry current drinkers, 9,870 African American current drinkers, 2,491 Asian ancestry current drinkers, 2,528 Hispanic current drinkers, 33,388 European ancestry non-drinkers, 11,119 African American non-drinkers, 9,959 Asian ancestry non-drinkers, 1,466 Hispanic non-drinkers 107,548 European ancestry current drinkers, 2,028 African American or Afro-Caribbean current drinkers, 41,240 Asian ancestry current drinkers, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals, 29,438 European ancestry non-drinkers, 2,447 African American or Afro-Caribbean non-drinkers, 67,191 Asian ancestry non-drinkers, 7,092 Hispanic non-drinkers, 1,668 Brazilian ancestry non-drinkers Affymetrix, Illumina [NR] (imputed) 0 triglyceride measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004329 GCST008080 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df) 56,505 European ancestry current drinkers, 9,870 African American current drinkers, 2,491 Asian ancestry current drinkers, 2,528 Hispanic current drinkers, 33,388 European ancestry non-drinkers, 11,119 African American non-drinkers, 9,959 Asian ancestry non-drinkers, 1,466 Hispanic non-drinkers 107,548 European ancestry current drinkers, 2,028 African American or Afro-Caribbean current drinkers, 41,240 Asian ancestry current drinkers, 6,622 Hispanic individuals, 1,984 Brazilian ancestry individuals, 29,438 European ancestry non-drinkers, 2,447 African American or Afro-Caribbean non-drinkers, 67,191 Asian ancestry non-drinkers, 7,092 Hispanic non-drinkers, 1,668 Brazilian ancestry non-drinkers Affymetrix, Illumina [NR] (imputed) 162 low density lipoprotein cholesterol measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004329 GCST008079 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) 44,831 European ancestry regular drinkers, 3,976 African American regular drinkers, 1,288 Asian ancestry regular drinkers, 827 Hispanic regular drinkers, 11,674 European ancestry non-regular drinkers, 5,894 African American non-regular drinkers, 1,203 Asian ancestry non-regular drinkers, 1,701 Hispanic non-regular drinkers 71,281 European ancestry regular drinkers, 711 African American or Afro-Caribbean regular drinkers, 35,088 Asian ancestry regular drinkers, 3,742 Hispanic regular drinkers, 36,267 European ancestry non-regular drinkers, 1,317 African American or Afro-Caribbean non-regular drinkers, 6,152 Asian ancestry non-regular drinkers, 2,880 Hispanic non-regular drinkers Affymetrix, Illumina [NR] (imputed) 153 low density lipoprotein cholesterol measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007878 GCST008078 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. LDL cholesterol levels 89,893 European ancestry individuals, 20,989 African American individuals, 12,450 Asian ancestry individuals, 3,994 HIspanic individuals 136,986 European ancestry individuals, 4,475 African American or Afro-Caribbean individuals, 108,431 Asian ancestry individuals, 13,714 Hispanic individuals, 3,652 Brazilian ancestry individuals Affymetrix, Illumina [NR] (imputed) 88 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008077 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Triglyceride levels 89,893 European ancestry individuals, 20,989 African American individuals, 12,450 Asian ancestry individuals, 3,994 HIspanic individuals 136,986 European ancestry individuals, 4,475 African American or Afro-Caribbean individuals, 108,431 Asian ancestry individuals, 13,714 Hispanic individuals, 3,652 Brazilian ancestry individuals Affymetrix, Illumina [NR] (imputed) 89 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008076 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) 44,831 European ancestry regular drinkers, 3,976 African American regular drinkers, 1,288 Asian ancestry regular drinkers, 827 Hispanic regular drinkers, 11,674 European ancestry non-regular drinkers, 5,894 African American non-regular drinkers, 1,203 Asian ancestry non-regular drinkers, 1,701 Hispanic non-regular drinkers 71,281 European ancestry regular drinkers, 711 African American or Afro-Caribbean regular drinkers, 35,088 Asian ancestry regular drinkers, 3,742 Hispanic regular drinkers, 36,267 European ancestry non-regular drinkers, 1,317 African American or Afro-Caribbean non-regular drinkers, 6,152 Asian ancestry non-regular drinkers, 2,880 Hispanic non-regular drinkers Affymetrix, Illumina [NR] (imputed) 226 alcohol consumption measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008075 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Triglyceride levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df) 44,831 European ancestry regular drinkers, 3,976 African American regular drinkers, 1,288 Asian ancestry regular drinkers, 827 Hispanic regular drinkers, 11,674 European ancestry non-regular drinkers, 5,894 African American non-regular drinkers, 1,203 Asian ancestry non-regular drinkers, 1,701 Hispanic non-regular drinkers 71,281 European ancestry regular drinkers, 711 African American or Afro-Caribbean regular drinkers, 35,088 Asian ancestry regular drinkers, 3,742 Hispanic regular drinkers, 36,267 European ancestry non-regular drinkers, 1,317 African American or Afro-Caribbean non-regular drinkers, 6,152 Asian ancestry non-regular drinkers, 2,880 Hispanic non-regular drinkers Affymetrix, Illumina [NR] (imputed) 162 triglyceride measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0007878 GCST008074 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (1df) 44,831 European ancestry regular drinkers, 3,976 African American regular drinkers, 1,288 Asian ancestry regular drinkers, 827 Hispanic regular drinkers, 11,674 European ancestry non-regular drinkers, 5,894 African American non-regular drinkers, 1,203 Asian ancestry non-regular drinkers, 1,701 Hispanic non-regular drinkers 71,281 European ancestry regular drinkers, 711 African American or Afro-Caribbean regular drinkers, 35,088 Asian ancestry regular drinkers, 3,742 Hispanic regular drinkers, 36,267 European ancestry non-regular drinkers, 1,317 African American or Afro-Caribbean non-regular drinkers, 6,152 Asian ancestry non-regular drinkers, 2,880 Hispanic non-regular drinkers Affymetrix, Illumina [NR] (imputed) 0 low density lipoprotein cholesterol measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007878 GCST008073 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. HDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (1df) 44,831 European ancestry regular drinkers, 3,976 African American regular drinkers, 1,288 Asian ancestry regular drinkers, 827 Hispanic regular drinkers, 11,674 European ancestry non-regular drinkers, 5,894 African American non-regular drinkers, 1,203 Asian ancestry non-regular drinkers, 1,701 Hispanic non-regular drinkers 71,281 European ancestry regular drinkers, 711 African American or Afro-Caribbean regular drinkers, 35,088 Asian ancestry regular drinkers, 3,742 Hispanic regular drinkers, 36,267 European ancestry non-regular drinkers, 1,317 African American or Afro-Caribbean non-regular drinkers, 6,152 Asian ancestry non-regular drinkers, 2,880 Hispanic non-regular drinkers Affymetrix, Illumina [NR] (imputed) 0 alcohol consumption measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008072 Genome-wide genotyping array 2019-07-05 30698716 de Vries PS 2019-01-29 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/30698716 Multi-Ancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. Triglyceride levels x alcohol consumption (regular vs non-regular drinkers) interaction (1df) 44,831 European ancestry regular drinkers, 3,976 African American regular drinkers, 1,288 Asian ancestry regular drinkers, 827 Hispanic regular drinkers, 11,674 European ancestry non-regular drinkers, 5,894 African American non-regular drinkers, 1,203 Asian ancestry non-regular drinkers, 1,701 Hispanic non-regular drinkers 71,281 European ancestry regular drinkers, 711 African American or Afro-Caribbean regular drinkers, 35,088 Asian ancestry regular drinkers, 3,742 Hispanic regular drinkers, 36,267 European ancestry non-regular drinkers, 1,317 African American or Afro-Caribbean non-regular drinkers, 6,152 Asian ancestry non-regular drinkers, 2,880 Hispanic non-regular drinkers Affymetrix, Illumina [NR] (imputed) 0 triglyceride measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0007878 GCST008071 Genome-wide genotyping array 2019-10-16 27130862 Sarnowski C 2016-04-06 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/27130862 Identification of a new locus at 16q12 associated with time to asthma onset. Asthma (time to onset) 5,462 European ancestry cases, 8,424 European ancestry controls NA Illumina [2387926] (imputed) 10 age of onset of asthma http://purl.obolibrary.org/obo/OBA_2001001 GCST008838 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Uveal melanoma 590 European ancestry cases, 5,199 European ancestry controls NA Illumina [10258281] (imputed) 10 Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000616 GCST009071 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Uveal melanoma with any chromosomal aberration 417 European ancestry cases, 5,199 European ancestry controls NA Illumina [10258281] (imputed) 5 Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000616 GCST009079 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Choroidal melanoma 438 European ancestry cases, 5,199 European ancestry controls NA Illumina [10258281] (imputed) 6 choroidal melanoma http://www.ebi.ac.uk/efo/EFO_0009093 GCST009078 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Uveal melanoma with chromosome 3 loss 253 European ancestry cases, 5,199 European ancestry controls NA Illumina [10258281] (imputed) 3 Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000616 GCST009077 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Uveal melanoma with epithelioid cells 285 European ancestry cases, 5,199 European ancestry controls NA Illumina [10258281] (imputed) 4 Epithelioid Cell Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000244 GCST009076 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Presence of epithelioid cells in uveal melanoma 285 European ancestry cases, 286 European ancestry controls NA Illumina [10258281] (imputed) 4 Epithelioid Cell Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000244 GCST009075 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Uveal melanoma (TNM stage 1 or 2) 330 European ancestry cases, 5,199 European ancestry controls NA Illumina [10258281] (imputed) 4 Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000616 GCST009074 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Uveal melanoma (TNM stage 3 or 4) 255 European ancestry cases, 5,199 European ancestry controls NA Illumina [10258281] (imputed) 3 Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000616 GCST009073 Genome-wide genotyping array 2019-11-19 31626034 Thomsen H 2019-10-11 Melanoma Res www.ncbi.nlm.nih.gov/pubmed/31626034 Genome-wide study on uveal melanoma patients finds association to DNA repair gene TDP1. Disease severity in uveal melanoma (TNM stage 3 or 4 vs TNM stage 1 or 2) 330 European ancestry stage 3 or 4 cases, 255 European ancestry stage 1 or 2 cases NA Illumina [10258281] (imputed) 5 uveal melanoma disease severity http://www.ebi.ac.uk/efo/EFO_0010244 GCST009072 Genome-wide genotyping array 2021-05-26 31610627 Lee YS 2019-09-26 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/31610627 In silico approach to calculate the transcript capacity. Body fat percentage 8,842 individuals NA Affymetrix [308003] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST011736 Genome-wide genotyping array 2019-11-18 31624269 Terao C 2019-10-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31624269 GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation. Mosaic loss of chromosome Y (Y chromosome dosage) 95,380 Japanese men NA Illumina [9591901] (imputed) 50 mosaic loss of chromosome Y measurement http://www.ebi.ac.uk/efo/EFO_0007783 GCST009066 Genome-wide genotyping array 2019-11-18 31624269 Terao C 2019-10-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31624269 GWAS of mosaic loss of chromosome Y highlights genetic effects on blood cell differentiation. Mosaic loss of chromosome Y (Y chromosome dosage) 205,011 men NA NR [NR] 36 mosaic loss of chromosome Y measurement http://www.ebi.ac.uk/efo/EFO_0007783 GCST009067 Genome-wide genotyping array 2019-08-13 31209380 Demontis D 2019-06-17 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/31209380 Genome-wide association study implicates CHRNA2 in cannabis use disorder. Mental disorder 35,006 Danish ancestry cases, 16,366 Danish ancestry controls NA Illumina [8969939] (imputed) 0 attention deficit hyperactivity disorder, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090 GCST008417 Genome-wide genotyping array 2019-08-13 31209380 Demontis D 2019-06-17 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/31209380 Genome-wide association study implicates CHRNA2 in cannabis use disorder. Psychiatric disorder without cannabis use disorder 32,716 Danish ancestry cases, 16,269 Danish ancestry controls NA Illumina [8969939] (imputed) 0 attention deficit hyperactivity disorder, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090 GCST008416 Genome-wide genotyping array 2019-08-13 31209380 Demontis D 2019-06-17 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/31209380 Genome-wide association study implicates CHRNA2 in cannabis use disorder. Cannabis use disorder vs schizophrenia 2,387 Danish ancestry cannabis use disorder cases, 1,789 Danish ancestry schizophrenia cases NA Illumina [8969939] (imputed) 0 cannabis dependence, schizophrenia, substance abuse http://www.ebi.ac.uk/efo/EFO_0007191, http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0002491 GCST008415 Genome-wide genotyping array 2019-08-13 31209380 Demontis D 2019-06-17 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/31209380 Genome-wide association study implicates CHRNA2 in cannabis use disorder. Cannabis use disorder 2,387 Danish ancestry cases, 48,985 Danish ancestry controls 5,501 Icelandic ancestry cases, 301,041 Icelandic ancestry controls Illumina [8969939] (imputed) 1 cannabis dependence, substance abuse http://www.ebi.ac.uk/efo/EFO_0007191, http://purl.obolibrary.org/obo/MONDO_0002491 GCST008414 Genome-wide genotyping array 2019-08-27 31295725 Wang ZT 2019-07-11 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/31295725 Genome-wide association study identifies CD1A associated with rate of increase in plasma neurofilament light in non-demented elders. Change in neurofilament light levels 545 European ancestry individuals NA Illumina [1231747] 5 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST008497 Genome-wide genotyping array 2020-01-17 31484785 Wright KM 2019-09-04 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31484785 A Prospective Analysis of Genetic Variants Associated with Human Lifespan. Parental longevity (father's age at death or father's attained age) up to 699,000 European ancestry individuals NA Illumina [458865] 48 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST009450 Genome-wide genotyping array 2020-01-17 31484785 Wright KM 2019-09-04 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31484785 A Prospective Analysis of Genetic Variants Associated with Human Lifespan. Parental longevity (mother's age at death or mother's attained age) up to 699,000 individuals NA Illumina [458525] 41 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST009449 Genome-wide genotyping array 2020-01-17 31484785 Wright KM 2019-09-04 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31484785 A Prospective Analysis of Genetic Variants Associated with Human Lifespan. Parental longevity (mother's age at death) 270,548 European ancestry individuals NA Illumina [541493] 17 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST009446 Genome-wide genotyping array 2020-01-17 31484785 Wright KM 2019-09-04 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31484785 A Prospective Analysis of Genetic Variants Associated with Human Lifespan. Parental longevity (father's age at death) 309,383 European ancestry individuals NA Illumina [541614] 27 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST009447 Genome-wide genotyping array 2020-01-17 31484785 Wright KM 2019-09-04 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31484785 A Prospective Analysis of Genetic Variants Associated with Human Lifespan. Longevity up to 482,000 European ancestry individuals NA Illumina [~ 540852] 87 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST009448 Genome-wide genotyping array 2019-11-04 31596875 Traylor M 2019-10-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/31596875 Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases. Joint damage in rheumatoid arthritis 2,527 European ancestry individuals, 196 African ancestry individuals, 52 individuals NA Affymetrix, Illumina [4802696] (imputed) 16 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST008992 Genome-wide genotyping array, Targeted genotyping array 2019-11-04 31596875 Traylor M 2019-10-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/31596875 Genetic associations with radiological damage in rheumatoid arthritis: Meta-analysis of seven genome-wide association studies of 2,775 cases. Joint damage in rheumatoid arthritis 2,527 European ancestry individuals NA Affymetrix, Illumina [2723488] (imputed) 14 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST008993 Genome-wide genotyping array, Targeted genotyping array 2019-09-22 30098192 Shaaban S 2018-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/30098192 Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. Esotropia 224 European ancestry accommodative cases, 826 European ancestry non-accommodative cases, 3,740 European ancestry controls 66 European ancestry accommodative cases, 689 European ancestry non-accommodative cases, 1,712 European ancestry controls Illumina [6470615] (imputed) 1 Esotropia http://purl.obolibrary.org/obo/HP_0000565 GCST008737 Genome-wide genotyping array 2019-09-22 30098192 Shaaban S 2018-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/30098192 Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. Accommodative esotropia 224 European ancestry cases, 749 European ancestry controls 66 European ancestry cases, 264 European ancestry controls Illumina [6470615] (imputed) 3 Accommodative esotropia http://purl.obolibrary.org/obo/HP_0020046 GCST008738 Genome-wide genotyping array 2019-09-22 30098192 Shaaban S 2018-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/30098192 Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. Amblyopia 386 European ancestry cases, 1,700 European ancestry controls 45 European ancestry cases, 180 European ancestry controls Illumina [6470615] (imputed) 15 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST008739 Genome-wide genotyping array 2019-09-22 30098192 Shaaban S 2018-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/30098192 Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. Hyperopia 361 European ancestry cases, 1,700 European ancestry controls 172 European ancestry cases, 690 European ancestry controls Illumina [6470615] (imputed) 4 hyperopia http://purl.obolibrary.org/obo/MONDO_0004891 GCST008740 Genome-wide genotyping array 2019-09-22 30098192 Shaaban S 2018-08-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/30098192 Genome-Wide Association Study Identifies a Susceptibility Locus for Comitant Esotropia and Suggests a Parent-of-Origin Effect. Non-accommodative esotropia 826 European ancestry cases, 2,991 European ancestry controls 689 European ancestry cases, 1,448 European ancestry controls Illumina [6470615] (imputed) 4 Non-accomodative esotropia http://purl.obolibrary.org/obo/HP_0031760 GCST008741 Genome-wide genotyping array 2020-01-16 31600487 Sazonovs A 2019-10-05 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/31600487 HLA-DQA1*05 Carriage Associated With Development of Anti-Drug Antibodies to Infliximab and Adalimumab in Patients With Crohn's Disease. Immunogenicity to anti-TNF therapy in Crohn's disease 1,240 European ancestry individuals 107 European ancestry individuals Illumina [7578947] (imputed) 0 response to TNF antagonist, anti-drug antibody measurement http://www.ebi.ac.uk/efo/EFO_0004653, http://www.ebi.ac.uk/efo/EFO_0010559 GCST009445 Genome-wide genotyping array 2019-10-16 31326317 Dai J 2019-07-17 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31326317 Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. Squamous cell lung carcinoma 3,860 Chinese ancestry cases, 4,490 European ancestry cases, 13,328 Chinese ancestry controls, 14,027 European ancestry controls NA Illumina [~ 11000000] (imputed) 3 squamous cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000708 GCST008835 Genome-wide genotyping array 2019-10-16 31326317 Dai J 2019-07-17 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31326317 Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. Lung adenocarcinoma 8,762 Chinese ancestry cases, 6,819 European ancestry cases, 13,328 Chinese ancestry controls, 14,027 European ancestry controls NA Illumina [~ 11000000] (imputed) 19 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST008836 Genome-wide genotyping array 2019-10-16 31326317 Dai J 2019-07-17 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31326317 Identification of risk loci and a polygenic risk score for lung cancer: a large-scale prospective cohort study in Chinese populations. Non-small cell lung cancer 13,327 Chinese ancestry cases, 13,793 European ancestry cases, 13,328 Chinese ancestry controls, 14,027 European ancestry controls NA Illumina [~ 11000000] (imputed) 28 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST008834 Genome-wide genotyping array 2019-12-12 31537151 Freitag-Wolf S 2019-09-19 J Dent Res www.ncbi.nlm.nih.gov/pubmed/31537151 Smoking Modifies the Genetic Risk for Early-Onset Periodontitis. Early onset periodontitis x smoking status interaction 499 European ancestry ever-smoker cases, 242 European ancestry never-smoker cases NA NR [79780573] (imputed) 3 smoking status measurement, aggressive periodontitis http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006342 GCST009253 Genome-wide genotyping array 2019-12-19 31606302 Schijven D 2019-10-09 Eur Neuropsychopharmacol www.ncbi.nlm.nih.gov/pubmed/31606302 Multivariate genome-wide analysis of stress-related quantitative phenotypes. Stress-related phenotypes (multivariate analysis) 583 European and other ancestry individuals NA Illumina [5361288] (imputed) 2 response to stress http://purl.obolibrary.org/obo/GO_0006950 GCST009326 Genome-wide genotyping array 2019-08-19 31289104 Kawamura Y 2019-07-08 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/31289104 Genome-wide association study revealed novel loci which aggravate asymptomatic hyperuricaemia into gout. Gout vs. Hyperuricemia 945 Japanese ancestry cases, 1,003 Japanese ancestry controls 1,915 Japanese ancestry cases, 2,146 Japanese ancestry controls Illumina [569200] 11 gout, hyperuricemia http://www.ebi.ac.uk/efo/EFO_0004274, http://www.ebi.ac.uk/efo/EFO_0009104 GCST008460 Genome-wide genotyping array 2019-11-18 31607149 Ramirez J 2019-10-14 Circ Arrhythm Electrophysiol www.ncbi.nlm.nih.gov/pubmed/31607149 Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics. T wave morphology restitution during exercise (MTAG) 51,574 European ancestry individuals NA NR [~ 9000000] (imputed) 8 T wave morphology measurement http://www.ebi.ac.uk/efo/EFO_0008398 GCST009068 Genome-wide genotyping array 2019-11-11 31607149 Ramirez J 2019-10-14 Circ Arrhythm Electrophysiol www.ncbi.nlm.nih.gov/pubmed/31607149 Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics. T wave morphology restitution during exercise 51,574 European ancestry individuals NA NR [~ 9000000] (imputed) 7 T wave morphology measurement http://www.ebi.ac.uk/efo/EFO_0008398 GCST009016 Genome-wide genotyping array 2019-11-18 31607149 Ramirez J 2019-10-14 Circ Arrhythm Electrophysiol www.ncbi.nlm.nih.gov/pubmed/31607149 Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics. T wave morphology restitution during recovery from exercise 51,574 European ancestry individuals NA NR [~ 9000000] (imputed) 8 T wave morphology measurement http://www.ebi.ac.uk/efo/EFO_0008398 GCST009069 Genome-wide genotyping array 2019-11-11 31607149 Ramirez J 2019-10-14 Circ Arrhythm Electrophysiol www.ncbi.nlm.nih.gov/pubmed/31607149 Cardiovascular Predictive Value and Genetic Basis of Ventricular Repolarization Dynamics. T wave morphology restitution during recovery from exercise (MTAG) 51,574 European ancestry individuals NA NR [~ 9000000] (imputed) 8 T wave morphology measurement http://www.ebi.ac.uk/efo/EFO_0008398 GCST009017 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Number of decayed, missing and filled tooth surfaces or use of dentures 14,976 European ancestry individuals with decayed, missing or filled tooth surface measurement, 11,816 Hispanic/Latino individuals with decayed, missing or filled tooth surface measurement, 77,714 European ancestry dentures cases, 383,317 European ancestry controls NA Affymetrix, Illumina [~ 8900000] (imputed) 47 dental caries, dentures http://www.ebi.ac.uk/efo/EFO_0003819, http://www.ebi.ac.uk/efo/EFO_0010078 GCST008295 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Number of decayed, missing and filled tooth surfaces 14,976 European ancestry individuals, 11,816 Hispanic/Latino individuals NA Affymetrix, Illumina [at least 8900000] (imputed) 2 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST008302 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Number of decayed and filled tooth surfaces per available tooth surface 14,717 European ancestry individuals, 11,816 Hispanic/Latino individuals NA Affymetrix, Illumina [at least 8900000] (imputed) 0 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST008299 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Periodontitis 17,353 European and Hispanic/Latino ancestry cases, 28,210 European and Hispanic/Latino ancestry controls, 1,680 Japanese ancestry cases, 15,670 Japanese ancestry controls NA Affymetrix, Illumina [at least 8900000] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST008300 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Bleeding gums 60,210 European ancestry cases, 400,821 European ancestry controls NA Affymetrix [at least 8900000] (imputed) 0 Gingival bleeding http://purl.obolibrary.org/obo/HP_0000225 GCST008301 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Painful gums 13,311 European ancestry cases, 447,720 European ancestry controls NA Affymetrix [at least 8900000] (imputed) 0 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST008303 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Dentures 77,714 European ancestry cases, 383,317 European ancestry controls NA Affymetrix [at least 8900000] (imputed) 47 dentures http://www.ebi.ac.uk/efo/EFO_0010078 GCST008306 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Toothache 18,959 European ancestry cases, 442,072 European ancestry controls NA Affymetrix [at least 8900000] (imputed) 0 toothache http://www.ebi.ac.uk/efo/EFO_0010072 GCST008305 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Mouth ulcers 47,091 European ancestry cases, 413,940 European ancestry controls NA Affymetrix [at least 8900000] (imputed) 0 Oral ulcer http://purl.obolibrary.org/obo/HP_0000155 GCST008304 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Number of natural teeth 16,133 European ancestry individuals, 11,816 hispanic/Latino individuals NA Affymetrix, Illumina [at least 8900000] (imputed) 0 number of teeth measurement http://www.ebi.ac.uk/efo/EFO_0010073 GCST008298 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Loose teeth 18,979 European ancestry cases, 442,052 European ancestry controls NA Affymetrix, Illumina [at least 8900000] (imputed) 0 periodontal measurement http://www.ebi.ac.uk/efo/EFO_0007780 GCST008297 Genome-wide genotyping array 2019-08-01 31235808 Shungin D 2019-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31235808 Genome-wide analysis of dental caries and periodontitis combining clinical and self-reported data. Periodontitis or loose teeth 17,353 European and Hispanic/Latino ancestry periodontitis cases, 18,979 European ancestry loose teeth cases, 470,262 European and Hispanic/latino ancestry controls NA Affymetrix, Illumina [~ 8900000] (imputed) 0 periodontitis, periodontal measurement http://www.ebi.ac.uk/efo/EFO_0000649, http://www.ebi.ac.uk/efo/EFO_0007780 GCST008296 Genome-wide genotyping array 2019-12-05 31649266 Gallagher CS 2019-10-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31649266 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Uterine fibroids and heavy menstrual bleeding 3,409 European ancestry cases, 199,171 European ancestry controls NA Affymetrix [10308721] (imputed) 7 uterine fibroid, Menorrhagia http://www.ebi.ac.uk/efo/EFO_0000731, http://purl.obolibrary.org/obo/HP_0000132 GCST009156 Genome-wide genotyping array 2019-12-05 31649266 Gallagher CS 2019-10-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31649266 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Heavy menstrual bleeding 9,813 European ancestry cases, 210,946 European ancestry controls NA Affymetrix [10308721] (imputed) 3 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST009157 Genome-wide genotyping array 2019-12-05 31649266 Gallagher CS 2019-10-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31649266 Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis. Uterine fibroids 20,406 European ancestry cases, 223,918 European ancestry controls 15,068 European ancestry cases, 43,587 European ancestry controls Affymetrix, Illumina [8662096] (imputed) 55 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST009158 Genome-wide genotyping array 2019-09-23 31477735 Liu X 2019-09-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31477735 Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Spontaneous preterm birth (preterm birth) 4,775 European ancestry cases, 60,148 European ancestry controls NA Illumina [7545601] (imputed) 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST008754 Genome-wide genotyping array 2019-09-23 31477735 Liu X 2019-09-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31477735 Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Early spontaneous preterm birth 1,139 European ancestry cases, 60,148 European ancestry controls 107 Finnish ancestry infant cases, 865 Finnish ancestry infant controls Illumina [7588467] (imputed) 2 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST008753 Genome-wide genotyping array 2019-09-23 31477735 Liu X 2019-09-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31477735 Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Post-term birth 7,888 European ancestry cases, 60,148 European ancestry controls 670 European ancestry infant cases, 5,626 European ancestry infant controls Illumina [7583965] (imputed) 1 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST008752 Genome-wide genotyping array 2019-09-23 31477735 Liu X 2019-09-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31477735 Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. Gestational age at birth (child effect) 84,689 European ancestry infants 9,291 European ancestry infants Illumina [7646297] (imputed) 1 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST008751 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Blood lipid levels (multivariate analysis) up to 188,577 individuals NA NR [up to 2004701] 0 total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004612 GCST011765 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Body morphological traits (multivariate analysis) up to 224,459 individuals NA NR [up to 2363881] 0 BMI-adjusted waist-hip ratio, body mass index, body height http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004339 GCST011764 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Red blood cell traits (multivariate analysis) up to 173,480 individuals NA NR [up to 8649095] 0 hemoglobin measurement, erythrocyte count, mean corpuscular hemoglobin concentration, mean corpuscular volume, hematocrit, mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0004527 GCST011763 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Blood pressure traits (multi-trait analysis) up to 69,395 individuals NA NR [2387851] 0 pulse pressure measurement, mean arterial pressure, diastolic blood pressure, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335 GCST011762 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Bone density traits (multivariate analysis) up to 32,965 individuals NA NR [8938035] 0 volumetric bone mineral density http://www.ebi.ac.uk/efo/EFO_0007620 GCST011761 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Kidney function traits (multivariate analysis) up to 67,093 individuals NA NR [2333498] 0 creatinine measurement, cystatin C measurement, chronic kidney disease, urinary albumin to creatinine ratio, Moderate albuminuria http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0004617, http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0007778, http://purl.obolibrary.org/obo/HP_0012594 GCST011760 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Fasting insulin, fasting glucose, HOMA-B, HOMA-IR (multivariate analysis) up to 46,186 individuals NA NR [2333328] 0 fasting blood glucose measurement, HOMA-B, HOMA-IR, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004465, http://www.ebi.ac.uk/efo/EFO_0004469, http://www.ebi.ac.uk/efo/EFO_0004501, http://www.ebi.ac.uk/efo/EFO_0004466 GCST011759 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Iron level traits (multivariate analysis) up to 48,972 individuals NA NR [1985313] 0 transferrin saturation measurement, ferritin measurement, transferrin measurement, serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006333, http://www.ebi.ac.uk/efo/EFO_0004459, http://www.ebi.ac.uk/efo/EFO_0006341, http://www.ebi.ac.uk/efo/EFO_0006332 GCST011758 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Number of children ever born and age at first birth (multivariate analysis) up to 343,072 individuals NA NR [2395561] 0 age at first birth measurement, number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009101, http://www.ebi.ac.uk/efo/EFO_0009102 GCST011757 Genome-wide genotyping array 2021-06-01 31596850 Turchin MC 2019-10-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31596850 Bayesian multivariate reanalysis of large genetic studies identifies many new associations. Brain structure volumes (multivariate analysis) up to 30,717 individuals NA NR [6271117] 0 pallidum volume, nucleus accumbens volume, hippocampal volume, intracranial volume measurement, putamen volume, amygdala volume, thalamus volume, caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0006933, http://www.ebi.ac.uk/efo/EFO_0006931, http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0004886, http://www.ebi.ac.uk/efo/EFO_0006932, http://www.ebi.ac.uk/efo/EFO_0006934, http://www.ebi.ac.uk/efo/EFO_0006935, http://www.ebi.ac.uk/efo/EFO_0004830 GCST011756 Genome-wide genotyping array 2019-09-12 31462767 Sun Y 2019-08-28 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31462767 Identification of novel risk loci with shared effects on alcoholism, heroin, and methamphetamine dependence. Alcohol dependence or heroin dependence or methamphetamine dependence 521 Han Chinese ancestry alcohol dependence cases, 1,026 Han Chinese ancestry heroin dependence cases, 1,749 Han Chinese ancestry methamphetamine dependence cases, 2,859 Han Chinese ancestry controls 146 Han Chinese ancestry alcohol dependence cases, 1,045 Han Chinese ancestry heroin dependence cases, 763 Han Chinese ancestry methamphetamine dependence cases, 1,904 Han Chinese ancestry controls Illumina [383065] (imputed) 3 alcohol dependence, heroin dependence, methamphetamine dependence http://purl.obolibrary.org/obo/MONDO_0007079, http://www.ebi.ac.uk/efo/EFO_0004240, http://www.ebi.ac.uk/efo/EFO_0004701 GCST008645 Genome-wide genotyping array 2019-09-24 31455332 Zhang Y 2019-08-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/31455332 Dissecting genetic factors affecting phenylephrine infusion rates during anesthesia: a genome-wide association study employing EHR data. Phenylephrine infusion rate during anesthesia 1,534 European ancestry individuals NA Illumina [up to 4929806] (imputed) 11 response to phenylephrine http://www.ebi.ac.uk/efo/EFO_0010152 GCST008755 Genome-wide genotyping array 2019-08-28 30571770 Arnau-Soler A 2018-12-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/30571770 Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. Stress sensitivity (neuroticism score x major depressive disorder status interaction) 2,010 European ancestry cases, 5,145 European ancestry controls NA NR [560698] (imputed) 10 unipolar depression, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007660 GCST008506 Genome-wide genotyping array 2019-08-28 30571770 Arnau-Soler A 2018-12-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/30571770 Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. Stress sensitivity (neuroticism score x major depressive disorder status interaction) 7,834 European ancestry cases, 15,258 European ancestry controls NA Affymetrix [557813] (imputed) 3 unipolar depression, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007660 GCST008507 Genome-wide genotyping array 2019-08-28 30571770 Arnau-Soler A 2018-12-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/30571770 Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. Stress sensitivity (neuroticism score x major depressive disorder status interaction) 9,844 European ancestry cases, 20,403 European ancestry controls NA Affymetrix [at least 557813] (imputed) 9 unipolar depression, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007660 GCST008508 Genome-wide genotyping array 2019-08-28 30571770 Arnau-Soler A 2018-12-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/30571770 Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. Major depressive disorder 9,844 European ancestry cases, 20,403 European ancestry controls NA Affymetrix [at least 557813] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST008509 Genome-wide genotyping array 2019-08-28 30571770 Arnau-Soler A 2018-12-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/30571770 Genome-wide interaction study of a proxy for stress-sensitivity and its prediction of major depressive disorder. Neuroticism 30,247 European ancestry individuals NA Affymetrix [at least 557813] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST008510 Genome-wide genotyping array 2019-10-23 31519223 Scepanovic P 2019-09-13 Microbiome www.ncbi.nlm.nih.gov/pubmed/31519223 A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals. Gut microbiota (beta diversity) 858 Metropolitan French ancestry individuals NA Illumina [5293637] (imputed) 47 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST008901 Genome-wide genotyping array, Exome genotyping array 2019-10-23 31519223 Scepanovic P 2019-09-13 Microbiome www.ncbi.nlm.nih.gov/pubmed/31519223 A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals. Gut microbiota (alpha diversity) 858 Metropolitan French ancestry individuals NA Illumina [5293637] (imputed) 47 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST008900 Genome-wide genotyping array, Exome genotyping array 2019-10-23 31519223 Scepanovic P 2019-09-13 Microbiome www.ncbi.nlm.nih.gov/pubmed/31519223 A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals. Gut microbiota relative abundance (bacterial taxa) up to 858 Metropolitan French ancestry individuals NA Illumina [5293637] (imputed) 58 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST008903 Genome-wide genotyping array, Exome genotyping array 2019-10-23 31519223 Scepanovic P 2019-09-13 Microbiome www.ncbi.nlm.nih.gov/pubmed/31519223 A comprehensive assessment of demographic, environmental, and host genetic associations with gut microbiome diversity in healthy individuals. Gut microbiota (bacterial taxa) 858 Metropolitan French ancestry individuals NA Illumina [5293637] (imputed) 23 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST008902 Genome-wide genotyping array, Exome genotyping array 2020-07-09 31605138 Avitabile M 2019-09-07 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/31605138 Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 gene. Neuroblastoma or malignant cutaneous melanoma 2,101 European ancestry neuroblastoma cases, 12,874 European ancestry malignant cutaneous melanoma cases, 27,405 European ancestry controls 2,039 European ancestry neuroblastoma cases, 508 European ancestry malignant cutaneous melanoma cases, 3,469 European ancestry controls NR [NR] (imputed) 16 neuroblastoma, cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0000621, http://www.ebi.ac.uk/efo/EFO_0000389 GCST010152 Genome-wide genotyping array 2019-10-21 31430377 Chung J 2019-08-20 Brain www.ncbi.nlm.nih.gov/pubmed/31430377 Genome-wide association study of cerebral small vessel disease reveals established and novel loci. Non-lobar intracerebral hemorrhage 1,005 European ancestry cases, 1,711 European ancestry controls NA Affymetrix, Illumina [39235000] (imputed) 2 non-lobar intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0010178 GCST008873 Genome-wide genotyping array 2019-10-21 31430377 Chung J 2019-08-20 Brain www.ncbi.nlm.nih.gov/pubmed/31430377 Genome-wide association study of cerebral small vessel disease reveals established and novel loci. Lobar intracerebral hemorrhage 755 European ancestry cases, 1,711 European ancestry controls NA Affymetrix, Illumina [39235000] (imputed) 1 lobar intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0010177 GCST008874 Genome-wide genotyping array 2019-10-21 31430377 Chung J 2019-08-20 Brain www.ncbi.nlm.nih.gov/pubmed/31430377 Genome-wide association study of cerebral small vessel disease reveals established and novel loci. Intracerebral hemorrhage (MTAG) at least 1,808 European ancestry cases, at least 1,711 European ancestry controls NA Affymetrix, Illumina [39235000] (imputed) 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST008875 Genome-wide genotyping array 2019-10-21 31430377 Chung J 2019-08-20 Brain www.ncbi.nlm.nih.gov/pubmed/31430377 Genome-wide association study of cerebral small vessel disease reveals established and novel loci. Non-lobar intracerebral hemorrhage (MTAG) at least 1,005 European ancestry cases, at least 1,711 European ancestry controls NA Affymetrix, Illumina [39235000] (imputed) 42 non-lobar intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0010178 GCST008876 Genome-wide genotyping array 2019-10-21 31430377 Chung J 2019-08-20 Brain www.ncbi.nlm.nih.gov/pubmed/31430377 Genome-wide association study of cerebral small vessel disease reveals established and novel loci. Lobar intracerebral hemorrhage (MTAG) at least 755 European ancestry cases, at least 1,711 European ancestry controls NA Affymetrix, Illumina [39235000] (imputed) 0 lobar intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0010177 GCST008877 Genome-wide genotyping array 2019-10-21 31430377 Chung J 2019-08-20 Brain www.ncbi.nlm.nih.gov/pubmed/31430377 Genome-wide association study of cerebral small vessel disease reveals established and novel loci. Intracerebral hemorrhage 1,808 European ancestry cases, 1,711 European ancestry controls NA Affymetrix, Illumina [39235000] (imputed) 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST008878 Genome-wide genotyping array 2019-10-28 31044621 Rimpela JM 2019-05-02 Blood Press www.ncbi.nlm.nih.gov/pubmed/31044621 Genome-wide association study of white-coat effect in hypertensive patients. White coat effect (clinic systolic blood pressure minus ambulatory systolic blood pressure) 206 Finnish ancestry individuals NA Illumina [629414] 4 response to stress, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0006950, http://www.ebi.ac.uk/efo/EFO_0006944 GCST008968 Genome-wide genotyping array 2019-10-28 31044621 Rimpela JM 2019-05-02 Blood Press www.ncbi.nlm.nih.gov/pubmed/31044621 Genome-wide association study of white-coat effect in hypertensive patients. White coat effect (clinic diastolic blood pressure minus ambulatory diastolic blood pressure) 206 Finnish ancestry individuals NA Illumina [629414] 6 diastolic blood pressure change measurement, response to stress http://www.ebi.ac.uk/efo/EFO_0006945, http://purl.obolibrary.org/obo/GO_0006950 GCST008969 Genome-wide genotyping array 2019-10-23 31564439 Fang H 2019-09-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31564439 Harmonizing Genetic Ancestry and Self-identified Race/Ethnicity in Genome-wide Association Studies. Height up to 248,507 non-Hispanic white individuals, up to 68,155 non-Hispanic black individuals, up to 25,847 Hispanic individuals, up to 3,054 Asian ancestry individuals NA Affymetrix [723305] 39 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST008904 Genome-wide genotyping array 2019-11-04 31600170 Teumer A 2019-10-10 JCI Insight www.ncbi.nlm.nih.gov/pubmed/31600170 KCND3 potassium channel gene variant confers susceptibility to electrocardiographic early repolarization pattern. Early cardiac repolarization 3,305 European ancestry cases, 36,151 European ancestry controls NA Affymetrix, Illumina [up to 6976246] (imputed) 7 early cardiac repolarization measurement http://www.ebi.ac.uk/efo/EFO_0004885 GCST008991 Genome-wide genotyping array 2019-10-15 31118516 Flannick J 2019-05-22 Nature www.ncbi.nlm.nih.gov/pubmed/31118516 Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Type 2 diabetes 2,277 African American cases, 3,098 East Asian ancestry cases, 3,704 European ancestry cases, 6,215 Hispanic/Latino cases, 2,939 South Asian ancestry cases, 2,283 African American controls, 2,921 East Asian ancestry controls, 3,514 European ancestry controls, 5,939 Hispanic/Latino controls, 3,022 South Asian ancestry controls NA Affymetrix, Illumina [up to 35256845] (imputed) 25 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST008833 Genome-wide genotyping array 2020-02-25 31628463 Chai JF 2019-10-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31628463 Associations with metabolites in Chinese suggest new metabolic roles in Alzheimer's and Parkinson's diseases. Metabolite levels 1,954 Chinese ancestry individuals NA Illumina [~ 47000000] (imputed) 134 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST009698 Genome-wide genotyping array 2019-12-18 31620175 Kornilov SA 2019-09-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/31620175 Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia. General cognitive ability 354 Saudi Arabian ancestry children NA Illumina [285340] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST009320 Genome-wide genotyping array 2019-12-18 31620175 Kornilov SA 2019-09-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/31620175 Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia. Verbal cognitive ability 354 Saudi Arabian ancestry children NA Illumina [285340] 1 cognitive function measurement, language measurement http://www.ebi.ac.uk/efo/EFO_0008354, http://www.ebi.ac.uk/efo/EFO_0007797 GCST009321 Genome-wide genotyping array 2019-12-18 31620175 Kornilov SA 2019-09-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/31620175 Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia. Numerical cognitive ability 354 Saudi Arabian ancestry children NA Illumina [285340] 6 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST009322 Genome-wide genotyping array 2019-12-18 31620175 Kornilov SA 2019-09-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/31620175 Genome-Wide Homozygosity Mapping Reveals Genes Associated With Cognitive Ability in Children From Saudi Arabia. Figural/spatial cognitive ability 354 Saudi Arabian ancestry children NA Illumina [285340] 3 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST009323 Genome-wide genotyping array 2019-08-06 29678681 Matana A 2018-04-18 Genomics www.ncbi.nlm.nih.gov/pubmed/29678681 Genome-wide meta-analysis identifies novel gender specific loci associated with thyroid antibodies level in Croatians. Plasma anti-thyroid peroxidase levels 1,593 Croatian ancestry women, 1,025 Croatian ancestry men NA Illumina [5527232] (imputed) 20 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST008368 Genome-wide genotyping array 2019-08-06 29678681 Matana A 2018-04-18 Genomics www.ncbi.nlm.nih.gov/pubmed/29678681 Genome-wide meta-analysis identifies novel gender specific loci associated with thyroid antibodies level in Croatians. Plasma anti-thyroglobulin and anti-thyroid peroxidase levels (bivariate analysis) up to 1,596 Croatian ancestry women, up to 1,033 Croatian ancestry men NA Illumina [5527232] (imputed) 19 thyroid peroxidase antibody measurement, anti-thyroglobulin antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666, http://www.ebi.ac.uk/efo/EFO_0009896 GCST008367 Genome-wide genotyping array 2019-08-06 29678681 Matana A 2018-04-18 Genomics www.ncbi.nlm.nih.gov/pubmed/29678681 Genome-wide meta-analysis identifies novel gender specific loci associated with thyroid antibodies level in Croatians. Plasma anti-thyroglobulin levels 1,596 Croatian ancestry women, 1,033 Croatian ancestry men NA Illumina [5527232] (imputed) 24 anti-thyroglobulin antibody measurement http://www.ebi.ac.uk/efo/EFO_0009896 GCST008369 Genome-wide genotyping array 2019-08-01 31299468 Condreay LD 2019-06-29 Respir Med www.ncbi.nlm.nih.gov/pubmed/31299468 Genetic effects on efficacy to fluticasone propionate/salmeterol treatment in COPD. Change in quality of life in response to fluticasone propionate/salmeterol in chronic obstructive pulmonary disease up to 1,209 European ancestry individuals, up to 136 African, African American, South East Asian, East Asian, American Indian/Alaskan Native, Mixed race, Arabic/North African, Central/South Asian or Japanese Asian ancestry individuals NA Affymetrix [> 10000000] (imputed) 1 response to corticosteroid, response to salmeterol, respiratory symptom change measurement http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0010062, http://www.ebi.ac.uk/efo/EFO_0010068 GCST008292 Genome-wide genotyping array 2019-08-01 31299468 Condreay LD 2019-06-29 Respir Med www.ncbi.nlm.nih.gov/pubmed/31299468 Genetic effects on efficacy to fluticasone propionate/salmeterol treatment in COPD. Response to fluticasone propionate/salmeterol in chronic obstructive pulmonary disease 530 European, African, African American, South East Asian, East Asian, American Indian/Alaskan Native, Mixed race, Arabic/North African, Central/South Asian or Japanese Asian ancestry treated cases, 658 European, African, African American, South East Asian, East Asian, American Indian/Alaskan Native, Mixed race, Arabic/North African, Central/South Asian or Japanese Asian ancestry untreated cases NA Affymetrix [> 10000000] (imputed) 1 respiratory symptom measurement, response to corticosteroid, response to salmeterol http://www.ebi.ac.uk/efo/EFO_0007939, http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0010062 GCST008294 Genome-wide genotyping array 2019-08-01 31299468 Condreay LD 2019-06-29 Respir Med www.ncbi.nlm.nih.gov/pubmed/31299468 Genetic effects on efficacy to fluticasone propionate/salmeterol treatment in COPD. Change in trough FEV1 in response to fluticasone propionate/salmeterol in chronic obstructive pulmonary disease 1,869 European ancestry individuals, 55 African American or African ancestry individuals, 33 South East Asian ancestry individuals, 33 East Asian ancestry individuals, 7 American Indian/Alaskan Native ancestry individuals, 4 Mixed race individuals, 3 Arabic/North African ancestry individuals, 1 Central/South Asian ancestry individuals NA Affymetrix [> 10000000] (imputed) 0 FEV change measurement, response to corticosteroid, response to salmeterol http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0031960, http://www.ebi.ac.uk/efo/EFO_0010062 GCST008293 Genome-wide genotyping array 2019-08-22 26398853 Ye BD 2016-01-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/26398853 Identification of Ten Additional Susceptibility Loci for Ulcerative Colitis Through Immunochip Analysis in Koreans. Ulcerative colitis 705 Korean ancestry cases, 1,178 Korean ancestry controls 980 Korean ancestry cases, 2,694 Korean ancestry controls Illumina [536821] (imputed) 5 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST008483 Targeted genotyping array [ImmunoChip] 2020-01-16 30954325 Kamboh MI 2019-03-11 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30954325 Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain. Age-related cognitive decline (global cognition) (slope of z-scores) 1,145 European ancestry individuals NA Illumina [5600000] (imputed) 5 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST009444 Genome-wide genotyping array 2020-01-16 30954325 Kamboh MI 2019-03-11 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30954325 Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain. Age-related cognitive decline (executive function) (slope of z-scores) 1,145 European ancestry individuals NA Illumina [5600000] (imputed) 9 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST009442 Genome-wide genotyping array 2020-01-16 30954325 Kamboh MI 2019-03-11 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30954325 Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain. Age-related cognitive decline (language) (slope of z-scores) 1,145 European ancestry individuals NA Illumina [5600000] (imputed) 28 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST009439 Genome-wide genotyping array 2020-01-16 30954325 Kamboh MI 2019-03-11 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30954325 Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain. Age-related cognitive decline (memory) (slope of z-scores) 1,145 European ancestry individuals NA Illumina [5600000] (imputed) 18 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST009441 Genome-wide genotyping array 2020-01-16 30954325 Kamboh MI 2019-03-11 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30954325 Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain. Age-related cognitive decline (visuospatial skill) (slope of z-scores) 1,145 European ancestry individuals NA Illumina [5600000] (imputed) 7 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST009443 Genome-wide genotyping array 2020-01-16 30954325 Kamboh MI 2019-03-11 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30954325 Population-based genome-wide association study of cognitive decline in older adults free of dementia: identification of a novel locus for the attention domain. Age-related cognitive decline (attention/processing speed) (slope of z-scores) 1,145 European ancestry individuals NA Illumina [5600000] (imputed) 14 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST009440 Genome-wide genotyping array 2019-02-27 30542056 Petridis C 2018-12-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30542056 Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne. Acne (severe) 5,602 European ancestry cases, 21,120 European ancestry controls NA Illumina [up to 7441713] (imputed) 20 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST007234 Genome-wide genotyping array 2019-01-14 30124842 Yengo L 2018-08-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30124842 Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry. Body mass index 456,426 European ancestry individuals, 224,849 individuals NA NR [~ 2400000] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST006900 Genome-wide genotyping array 2019-01-14 30124842 Yengo L 2018-08-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30124842 Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry. Height 456,426 European ancestry individuals, 237,103 individuals NA NR [~ 2400000] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST006901 Genome-wide genotyping array 2019-03-25 30589442 Whitfield JB 2018-12-27 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30589442 Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Gamma glutamyl transferase levels in excessive alcohol consumption 951 individuals NA Illumina [~ 7800000] (imputed) 16 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST007376 Genome-wide genotyping array 2019-03-25 30589442 Whitfield JB 2018-12-27 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30589442 Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Alanine aminotransferase levels in excessive alcohol consumption 951 individuals NA Illumina [~ 7800000] (imputed) 28 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST007381 Genome-wide genotyping array 2019-03-25 30589442 Whitfield JB 2018-12-27 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30589442 Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Aspartate aminotransferase levels in excessive alcohol consumption 951 individuals NA Illumina [~ 7800000] (imputed) 19 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST007377 Genome-wide genotyping array 2019-03-25 30589442 Whitfield JB 2018-12-27 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30589442 Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Gamma glutamyl transferase levels in low alcohol consumption 8,716 individuals NA Illumina [~ 7800000] (imputed) 25 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST007380 Genome-wide genotyping array 2019-03-25 30589442 Whitfield JB 2018-12-27 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30589442 Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Alanine aminotransferase levels in low alcohol consumption 8,716 individuals NA Illumina [~ 7800000] (imputed) 16 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST007379 Genome-wide genotyping array 2019-03-25 30589442 Whitfield JB 2018-12-27 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30589442 Biomarker and genomic risk factors for liver function test abnormality in hazardous drinkers. Aspartate aminotransferase levels in low alcohol consumption 8,716 individuals NA Illumina [~ 7800000] (imputed) 39 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST007378 Genome-wide genotyping array 2019-03-17 30552317 Guo W 2018-12-14 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30552317 Exploratory genome-wide association analysis of response to ketamine and a polygenic analysis of response to scopolamine in depression. Response to ketamine in bipolar disorder or major depression (antidepressant effects) 157 European ancestry individuals NA Illumina [~ 6000000] (imputed) 7 depressive symptom measurement, response to ketamine http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0009748 GCST007316 Genome-wide genotyping array 2019-03-17 30552317 Guo W 2018-12-14 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30552317 Exploratory genome-wide association analysis of response to ketamine and a polygenic analysis of response to scopolamine in depression. Response to ketamine in bipolar disorder or major depression (dissociation effects) 90 European ancestry individuals NA Illumina [~ 6000000] (imputed) 12 response to ketamine, dissociation measurement http://www.ebi.ac.uk/efo/EFO_0009748, http://www.ebi.ac.uk/efo/EFO_0009750 GCST007317 Genome-wide genotyping array 2019-08-08 31178898 Lin BM 2019-05-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/31178898 Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study. End-stage kidney disease 584 African American cases, 282 Hispanic cases, 112 East Asian cases, 96 Native Hawaiian cases, 1 American Indian cases, 30 cases, 8,429 African American controls, 15,852 Hispanic controls, 3,536 East Asian controls, 2,892 Native Hawaiian controls, 49 American Indian controls, 936 controls NA Illumina [1438399] (imputed) 15 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST008395 Genome-wide genotyping array 2019-08-08 31178898 Lin BM 2019-05-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/31178898 Genetics of Chronic Kidney Disease Stages Across Ancestries: The PAGE Study. Mild to moderate chronic kidney disease 1,532 African American cases, 1,336 Hispanic cases, 575 East Asian cases, 608 Native Hawaiian cases, 42 American Indian cases, 57 cases, 13,761 African American controls, 19,317 Hispanic controls, 3,540 East Asian controls, 2,892 Native Hawaiian controls, 595 American Indian controls, 936 controls NA Illumina [1438399] (imputed) 12 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST008394 Genome-wide genotyping array 2019-10-01 31417091 Kou I 2019-08-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31417091 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. Adolescent idiopathic scoliosis 5,327 Japanese ancestry cases, 73,884 Japanese ancestry controls NA Illumina [9332516] (imputed) 26 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST008789 Genome-wide genotyping array 2019-10-01 31417091 Kou I 2019-08-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31417091 Genome-wide association study identifies 14 previously unreported susceptibility loci for adolescent idiopathic scoliosis in Japanese. Adolescent idiopathic scoliosis 5,004 Japanese ancestry female cases, 33,679 Japanese ancestry female controls NA Illumina [9332516] (imputed) 15 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST008788 Genome-wide genotyping array 2019-08-28 31263163 Liu CT 2019-07-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31263163 Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. Fasting glucose change 13,807 European ancestry individuals NA Affymetrix, Illumina [~ 25000000] (imputed) 3 fasting blood glucose change measurement http://www.ebi.ac.uk/efo/EFO_0010120 GCST008503 Genome-wide genotyping array 2019-08-28 31263163 Liu CT 2019-07-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31263163 Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. Fasting glucose change (long-term) 3,669 European ancestry individuals NA Affymetrix, Illumina [~ 25000000] (imputed) 11 fasting blood glucose change measurement http://www.ebi.ac.uk/efo/EFO_0010120 GCST008504 Genome-wide genotyping array 2019-08-28 31263163 Liu CT 2019-07-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31263163 Genome-wide Association Study of Change in Fasting Glucose over time in 13,807 non-diabetic European Ancestry Individuals. Fasting glucose change (short-term) 8,195 European ancestry individuals NA Affymetrix, Illumina [~ 25000000] (imputed) 4 fasting blood glucose change measurement http://www.ebi.ac.uk/efo/EFO_0010120 GCST008505 Genome-wide genotyping array 2019-09-22 30575882 Lotta LA 2018-12-01 JAMA www.ncbi.nlm.nih.gov/pubmed/30575882 Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors. Waist-to-hip ratio adjusted for BMI 660,648 European ancestry individuals NA Affymetrix [2446094] (imputed) 202 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST008733 Genome-wide genotyping array 2019-09-22 30575882 Lotta LA 2018-12-01 JAMA www.ncbi.nlm.nih.gov/pubmed/30575882 Association of Genetic Variants Related to Gluteofemoral vs Abdominal Fat Distribution With Type 2 Diabetes, Coronary Disease, and Cardiovascular Risk Factors. Waist-hip ratio 663,598 European ancestry individuals NA Affymetrix [2446094] (imputed) 202 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008734 Genome-wide genotyping array 2020-04-16 31407531 Do AN 2019-08-13 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/31407531 Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans. Left ventricular mass x antihypertensive treatment interaction up to 2,068 African American individuals up to 613 European ancestry individuals Affymetrix, Illumina [up to 2191657] (imputed) 3 response to antihypertensive drug, left ventricular mass http://www.ebi.ac.uk/efo/EFO_0005405, http://www.ebi.ac.uk/efo/EFO_0009289 GCST009835 Genome-wide genotyping array 2020-04-16 31407531 Do AN 2019-08-13 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/31407531 Genome-wide meta-analysis of SNP and antihypertensive medication interactions on left ventricular traits in African Americans. Relative wall thickness x antihypertensive treatment interaction up to 2,068 African American individuals up to 613 European ancestry individuals Affymetrix, Illumina [up to 2191661] (imputed) 2 response to antihypertensive drug, heart relative wall thickness http://www.ebi.ac.uk/efo/EFO_0005405, http://www.ebi.ac.uk/efo/EFO_0009286 GCST009836 Genome-wide genotyping array 2019-12-17 31594949 Nievergelt CM 2019-10-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31594949 International meta-analysis of PTSD genome-wide association studies identifies sex- and ancestry-specific genetic risk loci. Post-traumatic stress disorder 23,212 European ancestry cases, 4,363 African ancestry cases, 1,981 Latino and Native American ancestry cases, 151,447 European ancestry controls, 10,976 African ancestry controls, 3,722 Latino and Native American ancestry controls NA Affymetrix, Illumina [~ 1175791] (imputed) 7 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST009315 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Retinal arteriolar tortuosity 3,094 European ancestry individuals 1,413 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009420 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Maximum retinal arteriolar tortuosity 3,094 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009421 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Retinal venular tortuosity 3,094 European ancestry individuals 1,413 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009422 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Maximum retinal venular tortuosity 3,094 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009423 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Central retinal arteriolar equivalent 3,094 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009424 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Central retinal vein equivalent 3,094 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009425 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Retinal arteriole-to-venule ratio 3,094 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST009426 Genome-wide genotyping array 2020-01-13 31597446 Veluchamy A 2019-10-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31597446 Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. Optic disc radius 3,094 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 optic disc measurement http://www.ebi.ac.uk/efo/EFO_0006936 GCST009427 Genome-wide genotyping array 2019-12-11 31522824 Liu Y 2019-09-06 J Dermatol Sci www.ncbi.nlm.nih.gov/pubmed/31522824 Genome-wide scan identified genetic variants associated with skin aging in a Chinese female population. Skin aging measurement 1,534 Han Chinese ancestry women 964 European ancestry women Illumina [6328611] (imputed) 5 skin aging measurement http://www.ebi.ac.uk/efo/EFO_0008006 GCST009252 Genome-wide genotyping array 2019-12-11 31522824 Liu Y 2019-09-06 J Dermatol Sci www.ncbi.nlm.nih.gov/pubmed/31522824 Genome-wide scan identified genetic variants associated with skin aging in a Chinese female population. Skin aging measurement 1,084 Han Chinese ancestry women (>50 years old) 964 European ancestry women Illumina [6328611] (imputed) 4 skin aging measurement http://www.ebi.ac.uk/efo/EFO_0008006 GCST009251 Genome-wide genotyping array 2019-10-25 31619474 Zhu Z 2019-10-17 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31619474 Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis. Asthma 46,802 European ancestry cases, 347,481 European ancestry controls 23,948 European and unknown ancestry cases, 118,538 European and unknown ancestry controls Affymetrix [8274727] (imputed) 130 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST008916 Genome-wide genotyping array 2019-10-25 31619474 Zhu Z 2019-10-17 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31619474 Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis. Asthma (childhood onset) 9,676 European ancestry cases, 347,481 European ancestry controls NA Affymetrix [8274727] (imputed) 2 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST008917 Genome-wide genotyping array 2019-10-25 31619474 Zhu Z 2019-10-17 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31619474 Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis. Asthma (adult onset) 22,296 European ancestry cases, 347,481 European ancestry controls NA Affymetrix [8274727] (imputed) 0 adult onset asthma http://www.ebi.ac.uk/efo/EFO_1002011 GCST008918 Genome-wide genotyping array 2019-10-25 31619474 Zhu Z 2019-10-17 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31619474 Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis. Asthma and attention deficit hyperactivity disorder 46,802 European ancestry asthma cases, 19,099 European ancestry attention deficit hyperactivity disorder cases, 381,675 European ancestry controls NA Affymetrix [up to 8274727] (imputed) 7 attention deficit hyperactivity disorder, asthma http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0004979 GCST008919 Genome-wide genotyping array 2019-10-25 31619474 Zhu Z 2019-10-17 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31619474 Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis. Asthma and anxiety disorder 46,802 European ancestry asthma cases, 5,710 European ancestry anxiety disorder cases, 359,081 European ancestry controls NA Affymetrix [up to 8274727] (imputed) 1 asthma, anxiety disorder http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0006788 GCST008920 Genome-wide genotyping array 2019-10-25 31619474 Zhu Z 2019-10-17 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31619474 Shared Genetics of Asthma and Mental Health Disorders: A Large-Scale Genome-Wide Cross-Trait Analysis. Asthma and major depressive disorder 46,802 European ancestry asthma cases, 59,851 European ancestry major depressive disorder cases, 460,635 European ancestry controls NA Affymetrix [up to 13554551] (imputed) 10 asthma, unipolar depression http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0003761 GCST008921 Genome-wide genotyping array 2019-09-02 31294817 Chen J 2019-07-11 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/31294817 Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes. Fagerstrӧm test for nicotine dependence 19,431 European ancestry individuals 7,010 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 nicotine dependence symptom count http://www.ebi.ac.uk/efo/EFO_0009262 GCST008548 Genome-wide genotyping array 2019-09-02 31294817 Chen J 2019-07-11 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/31294817 Genome-Wide Meta-Analyses of FTND and TTFC Phenotypes. Time to smoke first cigarette in the morning 18,567 European ancestry individuals 10,061 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 4 time to first cigarette measurement http://www.ebi.ac.uk/efo/EFO_0010126 GCST008547 Genome-wide genotyping array 2019-12-02 31301374 Noguchi E 2019-07-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31301374 HLA-DQ and RBFOX1 as susceptibility genes for an outbreak of hydrolyzed wheat allergy. Hydrolysed wheat protein allergy 452 Japanese ancestry cases, 2,700 Japaneses ancestry controls 45 Japanese ancestry cases, 326 Japaneses ancestry controls Illumina [6575663] (imputed) 2 wheat allergic reaction http://www.ebi.ac.uk/efo/EFO_1001243 GCST009143 Genome-wide genotyping array 2019-02-27 30527956 Rhodes CJ 2018-12-05 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/30527956 Genetic determinants of risk in pulmonary arterial hypertension: international genome-wide association studies and meta-analysis. Pulmonary arterial hypertension 2,085 European ancestry cases, 9,659 European ancestry controls NA Illumina [~ 7727590] (imputed) 3 pulmonary arterial hypertension http://www.ebi.ac.uk/efo/EFO_0001361 GCST007228 Genome-wide genotyping array, Genome-wide sequencing 2018-09-20 29931343 Haworth S 2018-06-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29931343 Consortium genome-wide meta-analysis for childhood dental caries traits. Childhood dental caries in primary teeth 6,922 European ancestry cases, 10,115 European ancestry controls, 7,530 cases, 11,473 controls NA Affymetrix, Illumina [at least 8640819] (imputed) 2 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST006312 Genome-wide genotyping array 2018-09-20 29931343 Haworth S 2018-06-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29931343 Consortium genome-wide meta-analysis for childhood dental caries traits. Childhood dental caries in permanent teeth 5,875 cases, 7,478 controls NA Affymetrix, Illumina [8734121] (imputed) 1 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST006311 Genome-wide genotyping array 2018-12-07 30275891 Das S 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30275891 Family-based genome-wide association of inflammation biomarkers and fenofibrate treatment response in the GOLDN study. Response to fenofibrate 778 individuals NA NR [243593] 0 response to fenofibrate http://purl.obolibrary.org/obo/GO_1901557 GCST006683 Genome-wide genotyping array 2018-12-07 30275891 Das S 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30275891 Family-based genome-wide association of inflammation biomarkers and fenofibrate treatment response in the GOLDN study. HDL cholesterol and triglyceride levels 821 individuals NA NR [NR] 16 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST006682 Genome-wide genotyping array 2019-01-25 30423114 Laufer VA 2018-11-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30423114 Genetic Influences on Susceptibility to Rheumatoid Arthritis in African-Americans. Rheumatoid arthritis 916 African American cases, 1,392 African American controls, 4,873 East Asian ancestry cases, 17,641 East Asian ancestry controls, 19,234 European ancestry cases, 61,654 European ancestry controls Illumina [8380626] (imputed) 190 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST006959 Genome-wide genotyping array 2019-04-24 30453627 Marklund M 2018-11-17 Nutrients www.ncbi.nlm.nih.gov/pubmed/30453627 Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity. Fatty acid desaturase activity (serum) 1,453 European ancestry individuals NA Illumina [at least 738879] (imputed) 6 fatty acid desaturase enzyme activity measurement http://www.ebi.ac.uk/efo/EFO_0009791 GCST007635 Genome-wide genotyping array 2019-04-24 30453627 Marklund M 2018-11-17 Nutrients www.ncbi.nlm.nih.gov/pubmed/30453627 Genome-Wide Association Studies of Estimated Fatty Acid Desaturase Activity in Serum and Adipose Tissue in Elderly Individuals: Associations with Insulin Sensitivity. Fatty acid desaturase activity (adipose tissue) 783 European ancestry individuals NA Illumina [1621833] (imputed) 2 fatty acid desaturase enzyme activity measurement http://www.ebi.ac.uk/efo/EFO_0009791 GCST007636 Genome-wide genotyping array 2019-10-29 30454882 Daily JW 2018-09-28 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/30454882 High genetic risk scores of SLIT3, PLEKHA5 and PPP2R2C variants increased insulin resistance and interacted with coffee and caffeine consumption in middle-aged adults. Insulin resistance/response 8,842 Korean ancestry individuals NA Affymetrix [NR] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST008975 Genome-wide genotyping array 2019-04-09 30478444 Demontis D 2018-11-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30478444 Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Attention deficit hyperactivity disorder 19,099 European ancestry cases, 72 non-European ancestry cases, 1,012 Han Chinese ancestry cases, 34,194 European ancestry controls, 72 non-European ancestry controls, 925 Han Chinese ancestry controls 5,085 Icelandic ancestry cases, 5,857 cases, 131,122 Icelandic ancestry controls, 70,393 controls Affymetrix, Illumina, Perlegen [8047421] (imputed) 15 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST007543 Genome-wide genotyping array 2019-09-16 30449631 Zeng X 2018-11-15 Environ Int www.ncbi.nlm.nih.gov/pubmed/30449631 Genome-wide interaction study of gene-by-occupational exposures on respiratory symptoms. Cough x occupational exposure (biological dust, mineral dust, gases and fumes, pesticides, aromatic solvents, chlorinated solvents, other solvents or metals) interaction 675 Dutch ancestry cough cases, 7,301 Dutch ancestry controls 584 Dutch ancestry cough cases, 6,205 Dutch ancestry controls Illumina [227981] 0 respiratory symptom measurement, environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0007939, http://www.ebi.ac.uk/efo/EFO_0008360 GCST008669 Genome-wide genotyping array 2019-09-16 30449631 Zeng X 2018-11-15 Environ Int www.ncbi.nlm.nih.gov/pubmed/30449631 Genome-wide interaction study of gene-by-occupational exposures on respiratory symptoms. Dyspnea x occupational exposure (biological dust, mineral dust, gases and fumes, pesticides, aromatic solvents, chlorinated solvents, other solvents or metals) interaction 547 Dutch ancestry dyspnea cases, 7,429 Dutch ancestry controls 505 Dutch ancestry dyspnea cases, 6,284 Dutch ancestry controls Illumina [227981] 0 respiratory symptom measurement, environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0007939, http://www.ebi.ac.uk/efo/EFO_0008360 GCST008670 Genome-wide genotyping array 2019-09-16 30449631 Zeng X 2018-11-15 Environ Int www.ncbi.nlm.nih.gov/pubmed/30449631 Genome-wide interaction study of gene-by-occupational exposures on respiratory symptoms. Phlegm x occupational exposure (biological dust, mineral dust, gases and fumes, pesticides, aromatic solvents, chlorinated solvents, other solvents or metals) interaction 1,702 Dutch ancestry phlegm cases, 6,274 Dutch ancestry controls 1,405 Dutch ancestry phlegm cases, 5,384 Dutch ancestry controls Illumina [227981] 0 respiratory symptom measurement, environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0007939, http://www.ebi.ac.uk/efo/EFO_0008360 GCST008671 Genome-wide genotyping array 2019-05-02 30487518 Takeuchi F 2018-11-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30487518 Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Systolic blood pressure 130,777 Japanese ancestry individuals 53,008 East Asian individuals, 105,253 European ancestry individuals Illumina [6200000] (imputed) 146 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST007703 Genome-wide genotyping array 2019-05-02 30487518 Takeuchi F 2018-11-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30487518 Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Diastolic blood pressure 130,777 Japanese ancestry individuals 53,008 East Asian individuals, 105,253 European ancestry individuals Illumina [6200000] (imputed) 122 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST007704 Genome-wide genotyping array 2019-05-02 30487518 Takeuchi F 2018-11-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30487518 Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Pulse pressure 130,777 Japanese ancestry individuals 53,008 East Asian individuals, 105,253 Japanese ancestry individuals Illumina [6200000] (imputed) 94 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST007705 Genome-wide genotyping array 2019-05-02 30487518 Takeuchi F 2018-11-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30487518 Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Mean arterial pressure 130,777 Japanese ancestry individuals 53,008 East Asian individuals, 105,253 European ancestry individuals Illumina [6200000] (imputed) 149 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST007706 Genome-wide genotyping array 2019-05-02 30487518 Takeuchi F 2018-11-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30487518 Interethnic analyses of blood pressure loci in populations of East Asian and European descent. Hypertension 22,566 Japanese ancestry cases, 28,226 Japanese ancestry controls 8,809 East Asian ancestry cases, 13,663 East Asian ancestry controls, 105,253 European ancestry individuals Illumina [6200000] (imputed) 106 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST007707 Genome-wide genotyping array 2019-01-21 29907492 Nakahara S 2018-06-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29907492 Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Attention function 2 Alaskan native ancestry schizophrenia cases, 18 Asian ancestry schizophrenia cases, 20 African American schizophrenia cases, 1 Native Hawaiian ancestry schizophrenia cases, 86 European ancestry schizophrenia cases, 2 Alaskan native ancestry controls, 10 Asian ancestry controls, 17 African American controls, 1 Native Hawaiian ancestry controls, 106 European ancestry controls NA Illumina [NR] (imputed) 1 attention function measurement http://www.ebi.ac.uk/efo/EFO_0007636 GCST006929 Genome-wide genotyping array 2019-01-21 29907492 Nakahara S 2018-06-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29907492 Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Working memory 2 Alaskan native ancestry schizophrenia cases, 18 Asian ancestry schizophrenia cases, 20 African American schizophrenia cases, 1 Native Hawaiian ancestry schizophrenia cases, 86 European ancestry schizophrenia cases, 2 Alaskan native ancestry controls, 10 Asian ancestry controls, 17 African American controls, 1 Native Hawaiian ancestry controls, 106 European ancestry controls NA Illumina [NR] (imputed) 3 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST006930 Genome-wide genotyping array 2019-01-21 29907492 Nakahara S 2018-06-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29907492 Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Verbal memory 2 Alaskan native ancestry schizophrenia cases, 18 Asian ancestry schizophrenia cases, 20 African American schizophrenia cases, 1 Native Hawaiian ancestry schizophrenia cases, 86 European ancestry schizophrenia cases, 2 Alaskan native ancestry controls, 10 Asian ancestry controls, 17 African American controls, 1 Native Hawaiian ancestry controls, 106 European ancestry controls NA Illumina [NR] (imputed) 3 verbal memory measurement http://www.ebi.ac.uk/efo/EFO_0009591 GCST006931 Genome-wide genotyping array 2019-01-21 29907492 Nakahara S 2018-06-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29907492 Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Visual memory 2 Alaskan native ancestry schizophrenia cases, 18 Asian ancestry schizophrenia cases, 20 African American schizophrenia cases, 1 Native Hawaiian ancestry schizophrenia cases, 86 European ancestry schizophrenia cases, 2 Alaskan native ancestry controls, 10 Asian ancestry controls, 17 African American controls, 1 Native Hawaiian ancestry controls, 106 European ancestry controls NA Illumina [NR] (imputed) 2 visual memory measurement http://www.ebi.ac.uk/efo/EFO_0009590 GCST006928 Genome-wide genotyping array 2019-01-21 29907492 Nakahara S 2018-06-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29907492 Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Reasoning 2 Alaskan native ancestry schizophrenia cases, 18 Asian ancestry schizophrenia cases, 20 African American schizophrenia cases, 1 Native Hawaiian ancestry schizophrenia cases, 86 European ancestry schizophrenia cases, 2 Alaskan native ancestry controls, 10 Asian ancestry controls, 17 African American controls, 1 Native Hawaiian ancestry controls, 106 European ancestry controls NA Illumina [NR] (imputed) 3 reasoning http://www.ebi.ac.uk/efo/EFO_0004350 GCST006932 Genome-wide genotyping array 2019-01-21 29907492 Nakahara S 2018-06-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29907492 Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Cognitive function 2 Alaskan native ancestry schizophrenia cases, 18 Asian ancestry schizophrenia cases, 20 African American schizophrenia cases, 1 Native Hawaiian ancestry schizophrenia cases, 86 European ancestry schizophrenia cases, 2 Alaskan native ancestry controls, 10 Asian ancestry controls, 17 African American controls, 1 Native Hawaiian ancestry controls, 106 European ancestry controls NA Illumina [NR] (imputed) 3 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST006933 Genome-wide genotyping array 2019-01-21 29907492 Nakahara S 2018-06-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29907492 Polygenic risk score, genome-wide association, and gene set analyses of cognitive domain deficits in schizophrenia. Information processing speed 2 Alaskan native ancestry schizophrenia cases, 18 Asian ancestry schizophrenia cases, 20 African American schizophrenia cases, 1 Native Hawaiian ancestry schizophrenia cases, 86 European ancestry schizophrenia cases, 2 Alaskan native ancestry controls, 10 Asian ancestry controls, 17 African American controls, 1 Native Hawaiian ancestry controls, 106 European ancestry controls NA Illumina [NR] (imputed) 1 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST006934 Genome-wide genotyping array 2019-10-30 30397551 Dorani F 2018-10-29 PeerJ www.ncbi.nlm.nih.gov/pubmed/30397551 Ensemble learning for detecting gene-gene interactions in colorectal cancer. Colorectal cancer 472 cases, 472 controls NA Affymetrix [186251] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST008977 Genome-wide genotyping array 2019-04-17 30392061 Orlova E 2018-11-03 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30392061 Genetic association and differential expression of PITX2 with acute appendicitis. Appendicitis 18,773 European ancestry cases, 114,907 European ancestry controls 59 European ancestry cases, 607 European ancestry controls, 7,267 Icelandic ancestry cases, 327,134 Icelandic ancestry controls, 1,139 Dutch ancestry cases, 4,587 Dutch ancestry controls Illumina [NR] (imputed) 1 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST007595 Genome-wide genotyping array 2019-02-26 30500874 Kakuta Y 2018-11-29 J Crohns Colitis www.ncbi.nlm.nih.gov/pubmed/30500874 A genome-wide association study identifying RAP1A as a novel susceptibility gene for Crohn's disease in Japanese individuals. Crohn's disease 713 Japanese ancestry cases, 2,083 Japanese ancestry controls 770 Japanese ancestry cases, 852 Japanese ancestry controls NR [4335144] (imputed) 9 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST007216 Genome-wide genotyping array 2019-08-16 31270906 Lai D 2019-07-03 Addict Biol www.ncbi.nlm.nih.gov/pubmed/31270906 Genome-wide association studies of the self-rating of effects of ethanol (SRE). Number of alcoholic drinks required to feel an effect (first five times drinking) 4,723 European ancestry individuals from 956 families, 1,527 African American individuals from 309 families 306 European ancestry individuals, 169 African American individuals Illumina [up to 15464468] (imputed) 1 response to alcohol http://www.ebi.ac.uk/efo/EFO_0005526 GCST008446 Genome-wide genotyping array 2019-08-16 31270906 Lai D 2019-07-03 Addict Biol www.ncbi.nlm.nih.gov/pubmed/31270906 Genome-wide association studies of the self-rating of effects of ethanol (SRE). Number of alcoholic drinks required to feel an effect (long-term average) 4,723 European ancestry individuals from 956 families, 1,527 African American individuals from 309 families 306 European ancestry individuals, 169 African American individuals Illumina [up to 15464468] (imputed) 2 response to alcohol http://www.ebi.ac.uk/efo/EFO_0005526 GCST008447 Genome-wide genotyping array 2019-02-11 30012220 Prins BP 2018-07-17 Genome Biol www.ncbi.nlm.nih.gov/pubmed/30012220 Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. QRS duration up to 77,898 European ancestry individuals, up to 7,695 African American individuals up to 111,874 European ancestry individuals Illumina [162199] 28 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST007104 Exome genotyping array [Exome array] 2019-02-11 30012220 Prins BP 2018-07-17 Genome Biol www.ncbi.nlm.nih.gov/pubmed/30012220 Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. QRS duration 77,898 European ancestry individuals NA Illumina [213295] 28 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST007103 Exome genotyping array [Exome array] 2019-02-11 30012220 Prins BP 2018-07-17 Genome Biol www.ncbi.nlm.nih.gov/pubmed/30012220 Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6. QRS duration 7,695 African American individuals NA Illumina [164799] 1 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST007105 Exome genotyping array [Exome array] 2018-06-01 29535710 Wahl A 2018-02-26 Front Immunol www.ncbi.nlm.nih.gov/pubmed/29535710 Genome-Wide Association Study on Immunoglobulin G Glycosylation Patterns. IgG glycosylation patterns 1,823 European ancestry individuals 1,836 European ancestry individuals Affymetrix [up to 18185628] (imputed) 310 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST005656 Genome-wide genotyping array 2017-05-12 28030426 Mahmoudpour SH 2017-03-27 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/28030426 Meta-analysis of genome-wide association studies on the intolerance of angiotensin-converting enzyme inhibitors. Angiotensin-converting enzyme inhibitor intolerance 972 European ancestry intolerant individuals, 4,189 European ancestry tolerant individuals NA Affymetrix, Illumina [NR] (imputed) 45 response to angiotensin-converting enzyme inhibitor http://www.ebi.ac.uk/efo/EFO_0005325 GCST004029 Genome-wide genotyping array 2017-04-11 28040410 Meyers JL 2016-12-28 Int J Psychophysiol www.ncbi.nlm.nih.gov/pubmed/28040410 A genome wide association study of fast beta EEG in families of European ancestry. Fast beta electroencephalogram 1,564 European ancestry individuals from 117 alcohol dependence affected families NA Illumina [12973748] (imputed) 5 alcohol dependence measurement, electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0007835, http://www.ebi.ac.uk/efo/EFO_0004357 GCST003902 Genome-wide genotyping array 2017-05-11 28031287 Sasayama D 2016-11-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/28031287 Genome-wide quantitative trait loci mapping of the human cerebrospinal fluid proteome. Cerebrospinal fluid biomarker levels 133 Japanese ancestry individuals. NA Illumina [514227] 65 cerebrospinal fluid biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006794 GCST004000 Genome-wide genotyping array 2017-05-12 28049566 Direk N 2016-12-08 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28049566 An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. Depressive symptom measurement or major depressive disorder 9,240 European ancestry cases, 9,519 European ancestry controls, 51,150 European ancestry individuals with depressive symptom measurement 6,879 European ancestry cases, 13,453 European ancestry controls, 5,303 Chinese ancestry cases, 5,337 Chinese ancestry controls, 8,157 European American individuals with depressive symptom measurement Affymetrix, Illumina, Perlegen [918921] (imputed) 2 unipolar depression, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007006 GCST004024 Genome-wide genotyping array 2017-06-27 28090653 Liu Y 2017-01-16 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/28090653 Genome-Wide Study Links PNPLA3 Variant With Elevated Hepatic Transaminase After Acute Lymphoblastic Leukemia Therapy. Alanine aminotransferase (ALT) levels after remission induction therapy in actute lymphoblastic leukemia (ALL) up to 488 European ancestry cases, up to 111 African American cases, up to 60 Hispanic cases, up to 56 other ancestry cases NA Affymetrix, Illumina [NR] (imputed) 54 serum alanine aminotransferase measurement, response to combination chemotherapy http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0007965 GCST004250 Genome-wide genotyping array 2019-01-21 30374069 Styrkarsdottir U 2018-10-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30374069 Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis. Knee osteoarthritis 23,877 European ancestry cases, 562,153 European ancestry controls NA Affymetrix, Illumina [11554240] (imputed) 7 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST006925 Genome-wide genotyping array 2019-01-21 30374069 Styrkarsdottir U 2018-10-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30374069 Meta-analysis of Icelandic and UK data sets identifies missense variants in SMO, IL11, COL11A1 and 13 more new loci associated with osteoarthritis. Osteoarthritis (hip) 17,151 European ancestry cases, 596,639 European ancestry controls NA Affymetrix, Illumina [11554240] (imputed) 32 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST006926 Genome-wide genotyping array 2019-01-29 30610198 Soler Artigas M 2019-01-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30610198 Attention-deficit/hyperactivity disorder and lifetime cannabis use: genetic overlap and causality. Attention deficit hyperactivity disorder or cannabis use 18,345 European ancestry ADHD cases, 14,374 European ancestry cannabis use cases, 50,410 European ancestry controls NA NR [5009020] (imputed) 16 attention deficit hyperactivity disorder, Cannabis use http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0007585 GCST006983 Genome-wide genotyping array 2019-07-11 31163085 Sharapov SZ 2019-06-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31163085 Defining the genetic control of human blood plasma N-glycome using genome-wide association study. N-glycan levels 2,763 individuals 327 Arab, South Asian and Filipino ancestry individuals, 294 European ancestry individuals, 591 individuals. Illumina [8557543] (imputed) 7 N-glycan measurement http://www.ebi.ac.uk/efo/EFO_0004999 GCST008108 Genome-wide genotyping array 2018-12-19 29998114 Gadad BS 2018-05-03 Mol Neuropsychiatry www.ncbi.nlm.nih.gov/pubmed/29998114 Association of Novel ALX4 Gene Polymorphisms with Antidepressant Treatment Response: Findings from the CO-MED Trial. Remission after antidepressant treatment in major depression 119 European ancestry remitters and non-remitters NA Illumina [232877] 0 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST006818 Genome-wide genotyping array 2018-12-19 29998114 Gadad BS 2018-05-03 Mol Neuropsychiatry www.ncbi.nlm.nih.gov/pubmed/29998114 Association of Novel ALX4 Gene Polymorphisms with Antidepressant Treatment Response: Findings from the CO-MED Trial. Response to antidepressants in depression 112 European ancestry responders, 98 European ancestry non-responders NA Illumina [232877] 5 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST006817 Genome-wide genotyping array 2019-08-05 31168069 Ward J 2019-06-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31168069 The genomic basis of mood instability: identification of 46 loci in 363,705 UK Biobank participants, genetic correlation with psychiatric disorders, and association with gene expression and function. Mood instability 157,039 European ancestry cases, 206,666 European ancestry controls NA Affymetrix [NR] (imputed) 46 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST008357 Genome-wide genotyping array 2019-09-18 31151762 Gelernter J 2019-04-08 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31151762 Genome-wide Association Study of Maximum Habitual Alcohol Intake in >140,000 U.S. European and African American Veterans Yields Novel Risk Loci. Maximum habitual alcohol consumption 126,936 European ancestry individuals, 17,029 African American individuals NA Affymetrix [up to 6007810] (imputed) 37 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST008675 Genome-wide genotyping array 2019-10-21 31598132 Donati G 2019-06-30 Mind Brain Educ www.ncbi.nlm.nih.gov/pubmed/31598132 Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education. Cognitive performance (processing speed) 4,611 European ancestry adolescents NA Illumina [6319684] (imputed) 22 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST008891 Genome-wide genotyping array 2019-10-21 31598132 Donati G 2019-06-30 Mind Brain Educ www.ncbi.nlm.nih.gov/pubmed/31598132 Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education. Working memory 4,611 European ancestry adolescents NA Illumina [6319684] (imputed) 18 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST008892 Genome-wide genotyping array 2019-10-21 31598132 Donati G 2019-06-30 Mind Brain Educ www.ncbi.nlm.nih.gov/pubmed/31598132 Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education. Inhibitory control 4,611 European ancestry adolescents NA Illumina [6319684] (imputed) 0 behavioural inhibitory control measurement http://www.ebi.ac.uk/efo/EFO_0008467 GCST008893 Genome-wide genotyping array 2020-01-15 30456811 Moss LC 2018-11-19 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30456811 Using Bayes model averaging to leverage both gene main effects and G ×  E interactions to identify genomic regions in genome-wide association studies. Asthma x air pollution interaction (2df) 606 Hispanic cases, 792 Hispanic controls, 643 European ancestry cases, 959 European ancestry controls NA NR [6212909] (imputed) 5 asthma, traffic air pollution measurement http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0007908 GCST009435 Genome-wide genotyping array 2020-01-15 30456811 Moss LC 2018-11-19 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30456811 Using Bayes model averaging to leverage both gene main effects and G ×  E interactions to identify genomic regions in genome-wide association studies. Asthma x Hispanic interaction (2df) 606 Hispanic cases, 792 Hispanic controls, 643 European ancestry cases, 959 European ancestry controls NA NR [6212909] (imputed) 4 asthma, Hispanic or Latin American http://purl.obolibrary.org/obo/MONDO_0004979, http://purl.obolibrary.org/obo/HANCESTRO_0014 GCST009434 Genome-wide genotyping array 2019-04-26 30453346 Tunjungputri RN 2018-11-19 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/30453346 The Inter-Relationship of Platelets with Interleukin-1β-Mediated Inflammation in Humans. Platelet count and reactivity phenotypes 534 European ancestry individuals NA Illumina [7000000] (imputed) 0 platelet reactivity measurement, platelet count http://www.ebi.ac.uk/efo/EFO_0004985, http://www.ebi.ac.uk/efo/EFO_0004309 GCST007652 Genome-wide genotyping array 2019-10-29 30459114 Jia X 2018-10-31 Int J Cardiol www.ncbi.nlm.nih.gov/pubmed/30459114 Multivariate analysis of genome-wide data to identify potential pleiotropic genes for type 2 diabetes, obesity and coronary artery disease using MetaCCA. Type 2 diabetes or obesity or coronary artery disease (pleiotropy) 234,069 European ancestry individuals, 48,286 European ancestry type 2 diabetes cases, 250,671 European ancestry type 2 diabetes controls, 22,233 European ancestry coronary artery disease cases, 64,762 European ancestry coronary artery disease controls NA NR [2382957] (imputed) 0 type 2 diabetes mellitus, obesity, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0001073, http://www.ebi.ac.uk/efo/EFO_0001645 GCST008976 Genome-wide genotyping array 2019-01-29 30498034 Terao C 2018-11-29 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/30498034 Genetic determinants and an epistasis of LILRA3 and HLA-B*52 in Takayasu arteritis. Takayasu arteritis 411 Japanese ancestry cases, 2,158 Japanese ancestry controls 219 Japanese ancestry cases, 3,770 Japanese ancestry controls Illumina [5878075] (imputed) 7 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST006984 Genome-wide genotyping array 2019-04-03 30410027 Gudmundsson J 2018-11-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30410027 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. Benign prostatic hyperplasia and lower urinary tract symptoms 20,621 European ancestry cases, 280,541 European ancestry controls NA Affymetrix, Illumina [42907111] (imputed) 23 lower urinary tract symptom, benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0008008, http://www.ebi.ac.uk/efo/EFO_0000284 GCST007507 Genome-wide genotyping array 2019-04-04 30410027 Gudmundsson J 2018-11-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30410027 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. Benign prostatic hyperplasia and lower urinary tract symptoms (prostate cancer excluded) 18,138 European ancestry cases, 277,213 European ancestry controls NA Affymetrix, Illumina [42907111] (imputed) 22 lower urinary tract symptom, benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0008008, http://www.ebi.ac.uk/efo/EFO_0000284 GCST007512 Genome-wide genotyping array 2019-04-03 30410027 Gudmundsson J 2018-11-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30410027 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. Prostate cancer 11,708 European ancestry cases, 284,184 European ancestry controls NA Affymetrix, Illumina [42907111] (imputed) 1 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST007506 Genome-wide genotyping array 2019-04-04 30410027 Gudmundsson J 2018-11-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30410027 Genome-wide associations for benign prostatic hyperplasia reveal a genetic correlation with serum levels of PSA. Prostate-specific antigen levels 33,572 Icelandic ancestry individuals NA Affymetrix, Illumina [up to 32463442] (imputed) 8 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST007513 Genome-wide genotyping array 2019-08-16 31269844 Wu NN 2019-07-03 J Matern Fetal Neonatal Med www.ncbi.nlm.nih.gov/pubmed/31269844 A genome-wide association study of gestational diabetes mellitus in Chinese women. Diabetes (gestational) 103 Han Chinese ancestry cases, 115 Han Chinese ancestry controls Illumina [65535] 3 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST008448 Genome-wide genotyping array 2019-08-19 31262040 Pujol-Moix N 2019-06-30 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/31262040 Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes. Platelet reactivity measurement (collagen-ADP) 935 Spanish ancestry individuals NA NR [10844567] (imputed) 1 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST008458 Genome-wide genotyping array 2019-08-19 31262040 Pujol-Moix N 2019-06-30 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/31262040 Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes. Platelet reactivity measurement (collagen-epinephrine) 935 Spanish ancestry individuals NA Illumina [10844567] (imputed) 1 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST008457 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Pulse rate 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals 1,620 individuals Illumina [212505] (imputed) 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST007051 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Lipoprotein (a) levels 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals NA Illumina [212505] (imputed) 10 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST007052 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Body mass index 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals 1,620 individuals Illumina [212505] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST007053 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Weight 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals 1,620 individuals Illumina [212505] (imputed) 2 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST007054 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Waist circumference 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals 1,620 individuals Illumina [212505] (imputed) 1 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST007055 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Waist-hip ratio 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals 1620 individuals Illumina [212505] (imputed) 1 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST007056 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Height 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals 1,620 individuals Illumina [212505] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST007057 Genome-wide genotyping array 2019-02-07 30108283 Granot-Hershkovitz E 2018-08-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30108283 A study of Kibbutzim in Israel reveals risk factors for cardiometabolic traits and subtle population structure. Hip circumference 733 Ashkenazi Jewish ancestry individuals (founder/population isolate), 168 Sephardi Jewish, North African Jewish, Middle Eastern, Caucasian and Yemenite Jewish individuals 1,620 individuals Illumina [212505] (imputed) 1 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST007058 Genome-wide genotyping array 2019-02-21 30456828 Khramtsova EA 2018-11-20 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/30456828 Sex differences in the genetic architecture of obsessive-compulsive disorder. Obsessive-compulsive disorder 1,249 European ancestry male cases, 2,789 European ancestry male controls, 1,525 European ancestry female cases, 4,307 European ancestry female controls NA NR [~ 5500000] (imputed) 20 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST007208 Genome-wide genotyping array 2019-02-21 30456828 Khramtsova EA 2018-11-20 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/30456828 Sex differences in the genetic architecture of obsessive-compulsive disorder. Obsessive-compulsive disorder x sex interaction 2,774 European ancestry cases, 7,096 European ancestry controls NA NR [~ 5500000] (imputed) 2 obsessive-compulsive disorder, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0008343 GCST007207 Genome-wide genotyping array 2019-10-24 31587654 Torres-Aguila NP 2019-10-07 Stroke www.ncbi.nlm.nih.gov/pubmed/31587654 Genome-Wide Association Study of White Blood Cell Counts in Patients With Ischemic Stroke. Leukocyte count in ischemic stroke 2,064 Spanish ancestry individuals 407 European ancestry individuals Illumina [7340003] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST008915 Genome-wide genotyping array 2019-11-04 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Waist-to-hip ratio adjusted for BMI 379,501 European ancestry female individuals NA NR [~ 27400000] (imputed) 258 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST008994 Genome-wide genotyping array 2019-11-04 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Waist-to-hip ratio adjusted for BMI 315,284 European ancestry male individuals NA NR [~ 27400000] (imputed) 84 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST008995 Genome-wide genotyping array 2019-11-04 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Waist-hip ratio 697,734 European ancestry individuals NA NR [~ 27400000] (imputed) 316 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008996 Genome-wide genotyping array 2019-11-04 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Waist-hip ratio 381,152 European female individuals NA NR [~ 27400000] (imputed) 195 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008997 Genome-wide genotyping array 2019-11-04 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Waist-hip ratio 316,772 European ancestry male individuals NA NR [~ 27400000] (imputed) 74 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008998 Genome-wide genotyping array 2019-11-05 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Body mass index 806,834 European ancestry individuals NA NR [~ 27400000] (imputed) 670 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009004 Genome-wide genotyping array 2019-11-05 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Body mass index 434,794 European ancestry female individuals NA NR [~ 27400000] (imputed) 281 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009003 Genome-wide genotyping array 2019-11-04 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Body mass index 374,756 European ancestry male individuals NA NR [~ 27400000] (imputed) 221 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009001 Genome-wide genotyping array 2019-11-04 30239722 Pulit SL 2018-09-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30239722 Meta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry. Waist-to-hip ratio adjusted for BMI 694,649 European ancestry individuals 7,721 European ancestry individuals NR [~ 27400000] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST008999 Genome-wide genotyping array 2019-02-06 29160301 Fabbri C 2017-11-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/29160301 New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation. Response to SSRI (symptom improvement) 1,828 European ancestry individuals 1,472 European ancestry individuals Affymetrix, Illumina [7062950] (imputed) 0 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST007042 Genome-wide genotyping array 2019-02-08 29160301 Fabbri C 2017-11-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/29160301 New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation. Response to antidepressants (symptom improvement) 2,145 European ancestry individuals NA Affymetrix, Illumina [7062950] (imputed) 18 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST007059 Genome-wide genotyping array 2019-02-08 29160301 Fabbri C 2017-11-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/29160301 New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation. Response to SSRI (symptom remission) 1,828 European ancestry individuals NA Affymetrix, Illumina [7062950] (imputed) 8 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST007060 Genome-wide genotyping array 2019-02-08 29160301 Fabbri C 2017-11-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/29160301 New insights into the pharmacogenomics of antidepressant response from the GENDEP and STAR*D studies: rare variant analysis and high-density imputation. Response to antidepressants (symptom remission) 2,145 European ancestry individuals NA Affymetrix, Illumina [7062950] (imputed) 11 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST007061 Genome-wide genotyping array 2019-01-29 30531825 Morgan MD 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531825 Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. Red vs. brown/black hair color 15,731 British ancestry red hair individuals, 283,920 British ancestry brown or black hair individuals NA Affymetrix [9154080] (imputed) 40 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST006986 Genome-wide genotyping array 2019-01-30 30531825 Morgan MD 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531825 Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. Blond vs. brown/black hair color 39,397 British ancestry blond hair individuals, 283,920 British ancestry brown or black hair individuals NA Affymetrix [9154080] (imputed) 213 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST006988 Genome-wide genotyping array 2019-01-30 30531825 Morgan MD 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531825 Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability. Brown vs. black hair color 269,394 British ancestry brown hair individuals, 14,526 British ancestry black hair individuals NA Affymetrix [9154080] (imputed) 56 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST006989 Genome-wide genotyping array 2018-11-16 30072576 Emilsson V 2018-08-02 Science www.ncbi.nlm.nih.gov/pubmed/30072576 Co-regulatory networks of human serum proteins link genetics to disease. Blood protein levels 3,200 European ancestry individuals NA Illumina [> 1000000] (imputed) 2992 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST006585 Targeted genotyping array 2019-03-07 30578418 Giri A 2018-12-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30578418 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Systolic blood pressure 365,998 European ancestry individuals, 63,490 African ancestry individuals, 22,802 Hispanic individuals, 4,792 Asian ancestry individuals, 2,695 Native American ancestry individuals 299,024 European ancestry individuals, 17,277 individuals Affymetrix [NR] (imputed) 340 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST007267 Genome-wide genotyping array 2019-03-07 30578418 Giri A 2018-12-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30578418 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Diastolic blood pressure 365,998 European ancestry individuals, 63,490 African ancestry individuals, 22,802 Hispanic individuals, 4,792 Asian ancestry individuals, 2,695 Native American ancestry individuals 299,024 European ancestry individuals, 17,277 individuals Affymetrix [NR] (imputed) 80 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST007268 Genome-wide genotyping array 2019-03-07 30578418 Giri A 2018-12-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30578418 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Pulse pressure 365,998 European ancestry individuals, 63,490 African ancestry individuals, 22,802 Hispanic individuals, 4,792 Asian ancestry individuals, 2,695 Native American ancestry individuals 299,024 European ancestry individuals, 17,277 individuals Affymetrix [NR] (imputed) 331 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST007269 Genome-wide genotyping array 2019-03-07 30578418 Giri A 2018-12-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30578418 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Systolic blood pressure 225,112 European ancestry individuals, 63,490 African ancestry individuals, 22,802 Hispanic individuals, 4,792 Asian ancestry individuals, 2,695 Native American ancestry individuals 445,360 individuals Affymetrix [NR] (imputed) 14 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST007270 Genome-wide genotyping array 2019-03-07 30578418 Giri A 2018-12-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30578418 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Diastolic blood pressure 225,112 European ancestry individuals, 63,490 African ancestry individuals, 22,802 Hispanic individuals, 4,792 Asian ancestry individuals, 2,695 Native American ancestry individuals 445,360 individuals Affymetrix [NR] (imputed) 4 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST007271 Genome-wide genotyping array 2019-03-07 30578418 Giri A 2018-12-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30578418 Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Pulse pressure 225,112 European ancestry individuals, 63,490 African ancestry individuals, 22,802 Hispanic individuals, 4,792 Asian ancestry individuals, 2,695 Native American ancestry individuals 445,360 individuals Affymetrix [NR] (imputed) 45 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST007272 Genome-wide genotyping array 2019-06-28 30591961 Huang L 2018-12-24 Sci China Life Sci www.ncbi.nlm.nih.gov/pubmed/30591961 Genome-wide analysis identified 17 new loci influencing intraocular pressure in Chinese population. Intraocular pressure 5,571 Chinese ancestry individuals 2,981 Chinese ancestry individuals Illumina [at least 900015] (imputed) 28 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST007998 Genome-wide genotyping array 2019-02-22 30578281 Williams LM 2018-12-01 Blood Adv www.ncbi.nlm.nih.gov/pubmed/30578281 A locus on chromosome 5 shows African ancestry-limited association with alloimmunization in sickle cell disease. Alloimmunization response to red blood cell transfusion in sickle cell anemia 144 African American cases, 123 African American controls 62 African American cases, 68 African American controls Illumina [1509415] 1 alloimmunization, response to red blood cell transfusion http://www.ebi.ac.uk/efo/EFO_0006804, http://www.ebi.ac.uk/efo/EFO_0006802 GCST007210 Genome-wide genotyping array 2020-02-11 31465739 Liu M 2019-08-26 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/31465739 A GENETIC VARIANT IN THE BCL2 GENE ASSOCIATES WITH ADALIMUMAB RESPONSE IN HIDRADENITIS SUPPURATIVA CLINICAL TRIALS AND REGULATES EXPRESSION OF BCL2. Response to adalimumab in hidradenitis suppurativa (abscess and inflammatory nodule count increase) 307 European ancestry individuals NR Illumina [6949858] (imputed) 1 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST009601 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Sweet taste perception in obesity with metabolic syndrome 378 individuals NA Illumina [622468] 6 sensory perception of taste http://purl.obolibrary.org/obo/GO_0050909 GCST008018 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Salty taste perception in obesity with metabolic syndrome 378 individuals NA Illumina [622468] 3 sensory perception of taste http://purl.obolibrary.org/obo/GO_0050909 GCST008024 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Sour taste perception in obesity with metabolic syndrome 378 individuals NA Illumina [622468] 2 sensory perception of taste http://purl.obolibrary.org/obo/GO_0050909 GCST008023 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Umami taste perception in obesity with metabolic syndrome 378 individuals NA Illumina [622468] 4 sensory perception of taste http://purl.obolibrary.org/obo/GO_0050909 GCST008022 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Taste perception (total score including phenylthiocarbamide) in obesity with metabolic syndrome 369 individuals NA Illumina [622468] 5 sensory perception of taste http://purl.obolibrary.org/obo/GO_0050909 GCST008020 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Taste perception (total score including 6-n-propylthiouracil) in obesity with metabolic syndrome up to 372 individuals NA Illumina [622468] 2 sensory perception of taste http://purl.obolibrary.org/obo/GO_0050909 GCST008021 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Bitter taste perception (6-n-propylthiouracil) in obesity with metabolic syndrome 368 individuals NA Illumina [622468] 8 sensory perception of bitter taste http://purl.obolibrary.org/obo/GO_0050913 GCST008017 Genome-wide genotyping array 2019-07-01 31005965 Coltell O 2019-04-21 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31005965 Association between taste perception and adiposity in overweight or obese older subjects with metabolic syndrome and identification of novel taste-related genes. Bitter taste perception (phenylthiocarbamide) in obesity with metabolic syndrome 372 individuals NA Illumina [622468] 10 sensory perception of bitter taste http://purl.obolibrary.org/obo/GO_0050913 GCST008019 Genome-wide genotyping array 2019-11-08 31469419 Manichaikul A 2019-08-30 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31469419 Identification of novel epithelial ovarian cancer loci in Women of African Ancestry. Epithelial ovarian cancer 755 African ancestry cases, 1,235 African ancestry controls NA Illumina [12486624] (imputed) 4 malignant epithelial tumor of ovary http://purl.obolibrary.org/obo/MONDO_0018364 GCST009008 Genome-wide genotyping array 2019-11-08 31469419 Manichaikul A 2019-08-30 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31469419 Identification of novel epithelial ovarian cancer loci in Women of African Ancestry. High-grade serous ovarian cancer 537 African ancestry cases, 1,235 African ancestry controls NA Illumina [11083029] (imputed) 6 ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_1001516 GCST009007 Genome-wide genotyping array 2019-01-21 30582445 Mola-Caminal M 2019-01-01 Circ Res www.ncbi.nlm.nih.gov/pubmed/30582445 PATJ Low Frequency Variants Are Associated With Worse Ischemic Stroke Functional Outcome. 3-month functional outcome in ischaemic stroke (modified Rankin score) 1,225 European ancestry individuals 1,791 European ancestry individuals Illumina [4480015] (imputed) 1 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST006935 Genome-wide genotyping array 2019-12-18 31502714 Wang J 2019-09-10 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31502714 Genome-wide association study of circulating folate one-carbon metabolites. Blood metabolite levels 1,788 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST009318 Genome-wide genotyping array 2019-02-08 30593698 Hubel C 2018-12-28 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/30593698 Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. Body fat percentage 70,700 European ancestry female individuals, 85,261 European ancestry male individuals NA Affymetrix [7794483] (imputed) 162 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST007064 Genome-wide genotyping array 2019-02-08 30593698 Hubel C 2018-12-28 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/30593698 Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. Fat-free mass 70,700 European ancestry female individuals, 85,261 European ancestry male individuals NA Affymetrix [7794483] (imputed) 407 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST007063 Genome-wide genotyping array 2019-07-12 31043756 Stahl EA 2019-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31043756 Genome-wide association study identifies 30 loci associated with bipolar disorder. Bipolar I disorder 14,879 European ancestry cases, 31,358 European ancestry controls NA NR [9372253] (imputed) 61 bipolar I disorder http://www.ebi.ac.uk/efo/EFO_0009963 GCST008115 Genome-wide genotyping array 2019-07-12 31043756 Stahl EA 2019-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31043756 Genome-wide association study identifies 30 loci associated with bipolar disorder. Bipolar II disorder 3,421 European ancestry cases, 31,358 European ancestry controls NA NR [9372253] (imputed) 5 bipolar II disorder http://www.ebi.ac.uk/efo/EFO_0009964 GCST008116 Genome-wide genotyping array 2019-07-12 31043756 Stahl EA 2019-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31043756 Genome-wide association study identifies 30 loci associated with bipolar disorder. Schizoaffective disorder-bipolar type 977 European ancestry cases, 31,358 European ancestry controls NA NR [9372253] (imputed) 10 Schizoaffective disorder-bipolar type http://www.ebi.ac.uk/efo/EFO_0009965 GCST008117 Genome-wide genotyping array 2019-07-09 31043756 Stahl EA 2019-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31043756 Genome-wide association study identifies 30 loci associated with bipolar disorder. Bipolar disorder 20,352 European ancestry cases, 31,358 European ancestry controls 9,412 European ancestry cases, 137,760 European ancestry controls NR [9372253] (imputed) 184 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST008103 Genome-wide genotyping array 2019-03-06 30583557 Loohuis LM 2018-12-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/30583557 The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. B6 vitamer levels (multivariate analysis) 493 European ancestry individuals NA Illumina [6260487] (imputed) 3 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST007260 Genome-wide genotyping array 2019-03-06 30583557 Loohuis LM 2018-12-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/30583557 The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. Cerebrospinal fluid pyridoxal phosphate levels 493 Dutch ancestry individuals NA Illumina [6260487] (imputed) 1 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST007261 Genome-wide genotyping array 2019-03-06 30583557 Loohuis LM 2018-12-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/30583557 The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. Plasma pyridoxal phosphate levels 493 Dutch ancestry individuals NA Illumina [6260487] (imputed) 1 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST007262 Genome-wide genotyping array 2019-03-06 30583557 Loohuis LM 2018-12-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/30583557 The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. Cerebrospinal fluid pyridoxal phosphate to pyridoxal ratio 493 Dutch ancestry individuals NA Illumina [6260487] (imputed) 1 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST007263 Genome-wide genotyping array 2019-03-06 30583557 Loohuis LM 2018-12-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/30583557 The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. Plasma pyridoxal phosphate to pyridoxal ratio 493 Dutch ancestry individuals NA Illumina [6260487] (imputed) 1 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST007264 Genome-wide genotyping array 2019-03-06 30583557 Loohuis LM 2018-12-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/30583557 The Alkaline Phosphatase (ALPL) Locus Is Associated with B6 Vitamer Levels in CSF and Plasma. Plasma pyridoxic acid to pyridoxal phosphate ratio 493 Dutch ancestry individuals NA Illumina [6260487] (imputed) 1 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST007265 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels x smoking (current vs non smokers) interaction (2df test) 5,120 African ancestry current smoker individuals, 2,394 Asian ancestry current smoker individuals, 15,129 European ancestry current smoker individuals, 747 Hispanic current smoker individuals, 18,641 African ancestry non smoker individuals, 10,777 Asian ancestry non smoker individuals, 75,138 European ancestry non smoker individuals, 5,873 Hispanic non smoker individuals 1,825 African ancestry current smoker individuals, 16,241 Asian ancestry current smoker individuals, 32,416 European ancestry current smoker individuals, 3,570 Hispanic current smoker individuals, 5,392 African ancestry non smoker individuals, 65,276 Asian ancestry non smoker individuals, 114,795 European ancestry non smoker individuals, 13,952 Hispanic non smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 8 smoking status measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008678 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels in current smokers 5,120 African ancestry individuals, 2,394 Asian ancestry individuals, 15,129 European ancestry individuals, 747 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008679 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels in non smokers 18,641 African ancestry individuals, 10,777 Asian ancestry individuals, 75,138 European ancestry individuals, 5,873 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008680 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels x smoking (ever vs never smokers) interaction (1df test) 11,893 African ancestry ever smoker individuals, 4,025 Asian ancestry ever smoker individuals, 49,475 European ancestry ever smoker individuals, 2,544 Hispanic ever smoker individuals, 11,866 African ancestry never smoker individuals, 9,146 Asian ancestry never smoker individuals, 40,797 European ancestry never smoker individuals, 4,076 Hispanic never smoker individuals 2,827 African ancestry ever smoker individuals, 37,952 Asian ancestry ever smoker individuals, 82,808 European ancestry ever smoker individuals, 7,091 Hispanic ever smoker individuals, 2,785 African ancestry never smoker individuals, 43,565 Asian ancestry never smoker individuals, 64,252 European ancestry never smoker individuals, 10,431 Hispanic never smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 2 smoking status measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008681 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels x smoking (ever vs never smokers) interaction (2df test) 11,893 African ancestry ever smoker individuals, 4,025 Asian ancestry ever smoker individuals, 49,475 European ancestry ever smoker individuals, 2,544 Hispanic ever smoker individuals, 11,866 African ancestry never smoker individuals, 9,146 Asian ancestry never smoker individuals, 40,797 European ancestry never smoker individuals, 4,076 Hispanic never smoker individuals 2,827 African ancestry ever smoker individuals, 37,952 Asian ancestry ever smoker individuals, 82,808 European ancestry ever smoker individuals, 7,091 Hispanic ever smoker individuals, 2,785 African ancestry never smoker individuals, 43,565 Asian ancestry never smoker individuals, 64,252 European ancestry never smoker individuals, 10,431 Hispanic never smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 5 smoking status measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008682 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels in ever smokers 11,893 African ancestry individuals, 4,025 Asian ancestry individuals, 49,475 European ancestry individuals, 2,544 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008683 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels in never smokers 11,866 African ancestry individuals, 9,146 Asian ancestry individuals, 40,797 European ancestry individuals, 4,076 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008684 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels up to 23,761 African ancestry individuals, 13,171 Asian ancestry individuals, up to 90,272 European ancestry individuals, 6,620 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 87 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008685 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels x smoking (current vs non smokers) interaction (1df test) 4,973 African ancestry current smoker individuals, 2,375 Asian ancestry current smoker individuals, 13,799 European ancestry current smoker individuals, 755 Hispanic current smoker individuals, 18,384 African ancestry non smoker individuals, 10,742 Asian ancestry non smoker individuals, 68,719 European ancestry non smoker individuals, 5,894 Hispanic non smoker individuals 1,357 African ancestry current smoker individuals, 8,901 Asian ancestry current smoker individuals, 25,008 European ancestry current smoker individuals, 3,441 Hispanic current smoker individuals, 3,967 African ancestry non smoker individuals, 39,448 Asian ancestry non smoker individuals, 92,432 European ancestry non smoker individuals, 13,555 Hispanic non smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 3 smoking status measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004611 GCST008686 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels x smoking (current vs non smokers) interaction (2df test) 4,973 African ancestry current smoker individuals, 2,375 Asian ancestry current smoker individuals, 13,799 European ancestry current smoker individuals, 755 Hispanic current smoker individuals, 18,384 African ancestry non smoker individuals, 10,742 Asian ancestry non smoker individuals, 68,719 European ancestry non smoker individuals, 5,894 Hispanic non smoker individuals 1,357 African ancestry current smoker individuals, 8,901 Asian ancestry current smoker individuals, 25,008 European ancestry current smoker individuals, 3,441 Hispanic current smoker individuals, 3,967 African ancestry non smoker individuals, 39,448 Asian ancestry non smoker individuals, 92,432 European ancestry non smoker individuals, 13,555 Hispanic non smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 5 smoking status measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004611 GCST008687 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels in current smokers 4,973 African ancestry individuals, 2,375 Asian ancestry individuals, 13,799 European ancestry individuals, 755 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008688 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels in non smokers 18,384 African ancestry individuals, 10,742 Asian ancestry individuals, 68,719 European ancestry individuals, 5,894 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008689 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels x smoking (ever vs never smokers) interaction (1df test) 11,649 African ancestry ever smoker individuals, 3,999 Asian ancestry ever smoker individuals, 45,506 European ancestry ever smoker individuals, 2,554 Hispanic ever smoker individuals, 11,700 African ancestry never smoker individuals, 9,118 Asian ancestry never smoker individuals, 37,016 European ancestry never smoker individuals, 4,095 Hispanic never smoker individuals 1,693 African ancestry ever smoker individuals, 20,368 Asian ancestry ever smoker individuals, 65,806 European ancestry ever smoker individuals, 6,857 Hispanic ever smoker individuals, 2,025 African ancestry never smoker individuals, 27,981 Asian ancestry never smoker individuals, 51,361 European ancestry never smoker individuals, 10,139 Hispanic never smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 2 smoking status measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004611 GCST008690 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels x smoking (ever vs never smokers) interaction (2df test) 11,649 African ancestry ever smoker individuals, 3,999 Asian ancestry ever smoker individuals, 45,506 European ancestry ever smoker individuals, 2,554 Hispanic ever smoker individuals, 11,700 African ancestry never smoker individuals, 9,118 Asian ancestry never smoker individuals, 37,016 European ancestry never smoker individuals, 4,095 Hispanic never smoker individuals 1,693 African ancestry ever smoker individuals, 20,368 Asian ancestry ever smoker individuals, 65,806 European ancestry ever smoker individuals, 6,857 Hispanic ever smoker individuals, 2,025 African ancestry never smoker individuals, 27,981 Asian ancestry never smoker individuals, 51,361 European ancestry never smoker individuals, 10,139 Hispanic never smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 4 smoking status measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004611 GCST008691 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels in ever smokers 11,649 African ancestry individuals, 3,999 Asian ancestry individuals, 45,506 European ancestry individuals, 2,554 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008692 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels in never smokers 11,700 African ancestry individuals, 9,118 Asian ancestry individuals, 37,016 European ancestry individuals, 4,095 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008693 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. LDL cholesterol levels up to 23,353 African ancestry individuals, 13,171 Asian ancestry individuals, up to 82,522 European ancestry individuals, 6,646 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 62 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008676 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels x smoking (current vs non smokers) interaction (1df test) 5,022 African ancestry current smoker individuals, 808 Asian ancestry current smoker individuals, 13,303 European ancestry current smoker individuals, 764 Hispanic current smoker individuals, 18,489 African ancestry non smoker individuals, 3,841 Asian ancestry non smoker individuals, 63,740 European ancestry non smoker individuals, 5,941 Hispanic non smoker individuals 1,367 African ancestry current smoker individuals, 22,744 Asian ancestry current smoker individuals, 22,268 European ancestry current smoker individuals, 2,899 Hispanic current smoker individuals, 3,989 African ancestry non smoker individuals, 89,177 Asian ancestry non smoker individuals, 86,885 European ancestry non smoker individuals, 11,811 Hispanic non smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 2 smoking status measurement, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004530 GCST008694 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels x smoking (current vs non smokers) interaction (2df test) 5,022 African ancestry current smoker individuals, 808 Asian ancestry current smoker individuals, 13,303 European ancestry current smoker individuals, 764 Hispanic current smoker individuals, 18,489 African ancestry non smoker individuals, 3,841 Asian ancestry non smoker individuals, 63,740 European ancestry non smoker individuals, 5,941 Hispanic non smoker individuals 1,367 African ancestry current smoker individuals, 22,744 Asian ancestry current smoker individuals, 22,268 European ancestry current smoker individuals, 2,899 Hispanic current smoker individuals, 3,989 African ancestry non smoker individuals, 89,177 Asian ancestry non smoker individuals, 86,885 European ancestry non smoker individuals, 11,811 Hispanic non smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 6 smoking status measurement, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004530 GCST008695 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels in current smokers 5,022 African ancestry individuals, 808 Asian ancestry individuals, 13,303 European ancestry individuals, 764 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008696 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels in non smokers 18,489 African ancestry individuals, 3,841 Asian ancestry individuals, 63,740 European ancestry individuals, 5,941 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008697 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels x smoking (ever vs never smokers) interaction (2df test) 11,735 African ancestry ever smoker individuals, 1,172 Asian ancestry ever smoker individuals, 42,899 European ancestry ever smoker individuals, 2,582 Hispanic ever smoker individuals, 11,777 African ancestry never smoker individuals, 3,477 Asian ancestry never smoker individuals, 34,148 European ancestry never smoker individuals, 4,123 Hispanic never smoker individuals 1,710 African ancestry ever smoker individuals, 54,217 Asian ancestry ever smoker individuals, 11,550 European ancestry ever smoker individuals, 5,915 Hispanic ever smoker individuals, 2,040 African ancestry never smoker individuals, 57,704 Asian ancestry never smoker individuals, 47,916 European ancestry never smoker individuals, 8,795 Hispanic never smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 4 smoking status measurement, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004530 GCST008698 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels x smoking (ever vs never smokers) interaction (1df test) 11,735 African ancestry ever smoker individuals, 1,172 Asian ancestry ever smoker individuals, 42,899 European ancestry ever smoker individuals, 2,582 Hispanic ever smoker individuals, 11,777 African ancestry never smoker individuals, 3,477 Asian ancestry never smoker individuals, 34,148 European ancestry never smoker individuals, 4,123 Hispanic never smoker individuals 1,710 African ancestry ever smoker individuals, 54,217 Asian ancestry ever smoker individuals, 11,550 European ancestry ever smoker individuals, 5,915 Hispanic ever smoker individuals, 2,040 African ancestry never smoker individuals, 57,704 Asian ancestry never smoker individuals, 60,675 European ancestry never smoker individuals, 8,795 Hispanic never smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 2 smoking status measurement, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004530 GCST008699 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels in ever smokers 11,735 African ancestry individuals, 1,172 Asian ancestry individuals, 42,899 European ancestry individuals, 2,582 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008700 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels in never smokers 11,777 African ancestry individuals, 3,477 Asian ancestry individuals, 34,148 European ancestry individuals, 4,123 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008701 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Epilepsy 14,534 European ancestry cases, 531 Han Chinese ancestry cases, 147 African American cases, 24,218 European ancestry controls, 2,875 Han Chinese ancestry controls, 2,584 African American controls NA Affymetrix, Illumina [~ 5000000] (imputed) 3 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST007343 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Childhood absence epilepsy 778 European ancestry cases, 24,218 European ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 2 childhood absence epilepsy http://purl.obolibrary.org/obo/MONDO_0010826 GCST007345 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Juvenile absence epilepsy 415 European ancestry cases, 24,218 European ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 0 juvenile absence epilepsy http://purl.obolibrary.org/obo/MONDO_0011876 GCST007346 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Juvenile myoclonic epilepsy 1,177 European ancestry cases, 4,218 European ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 1 juvenile myoclonic epilepsy http://purl.obolibrary.org/obo/MONDO_0009696 GCST007347 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Epilepsy (generalized, with tonic-clonic seizures alone) 225 European ancestry cases, 24,218 European ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 0 epilepsy with generalized tonic-clonic seizures http://www.ebi.ac.uk/efo/EFO_0007262 GCST007348 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Focal epilepsy (lesion negative) 2,660 European ancestry cases, 24,218 European ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 0 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST007349 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Focal epilepsy (with hippocampal sclerosis) 709 European ancestry cases, 24,218 European ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 2 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST007350 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Focal epilepsy (with lesion other than hippocampal sclerosis) 2,751 European ancestry cases, 24,218 European ancestry controls NA Affymetrix, Illumina [~ 5000000] (imputed) 0 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST007351 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Focal epilepsy 9,095 European ancestry cases, 490 Han Chinese ancestry cases, 86 African American cases, 24,218 European ancestry controls, 2,875 Han Chinese ancestry controls, 2,584 African American controls NA Affymetrix, Illumina [~ 5000000] (imputed) 1 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST007352 Genome-wide genotyping array 2019-03-19 30531953 International League Against Epilepsy Consortium on Complex Epilepsies 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531953 Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies. Generalized epilepsy 3,708 European ancestry cases, 61 African American cases, 24,218 European ancestry controls, 2,584 African American controls NA Affymetrix, Illumina [~ 5000000] (imputed) 11 generalised epilepsy http://www.ebi.ac.uk/efo/EFO_0005917 GCST007353 Genome-wide genotyping array 2019-04-24 30593799 Vergara C 2018-12-26 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/30593799 Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus. Hepatitis C (spontaneous viral clearance) 701 European ancestry cases, 1,035 European ancestry controls, 445 African American cases, 1,756 African American controls, 173 Hispanic ancestry cases, 313 Hispanic ancestry controls NA Illumina [15704341] (imputed) 3 remission, hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0009785, http://www.ebi.ac.uk/efo/EFO_0003047 GCST007631 Genome-wide genotyping array 2019-04-24 30593799 Vergara C 2018-12-26 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/30593799 Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus. Hepatitis C (spontaneous viral clearance) 445 African American cases, 1,756 African American controls NA Illumina [at least 15383342] (imputed) 1 remission, hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0009785, http://www.ebi.ac.uk/efo/EFO_0003047 GCST007632 Genome-wide genotyping array 2019-04-24 30593799 Vergara C 2018-12-26 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/30593799 Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus. Hepatitis C (spontaneous viral clearance) 701 European ancestry cases, 1,035 European ancestry controls NA Illumina [8968220] (imputed) 2 remission, hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0009785, http://www.ebi.ac.uk/efo/EFO_0003047 GCST007633 Genome-wide genotyping array 2019-04-24 30593799 Vergara C 2018-12-26 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/30593799 Multi-Ancestry Genome-Wide Association Study of Spontaneous Clearance of Hepatitis C Virus. Hepatitis C (spontaneous viral clearance) 173 Hispanic ancestry cases, 313 Hispanic ancestry controls NA Illumina [12650831] (imputed) 1 remission, hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0009785, http://www.ebi.ac.uk/efo/EFO_0003047 GCST007634 Genome-wide genotyping array 2019-04-17 30578877 Dahlin A 2018-12-19 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/30578877 Large-scale, multi-ethnic genome-wide association study identifies novel loci contributing to asthma susceptibility in adults. Adult asthma 16,274 European ancestry cases, 38,269 European ancestry controls 10,365 European ancestry cases, 16,110 European ancestry controls, cases and controls (see Moffatt et al 2010) Affymetrix [7230512] (imputed) 3 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007596 Genome-wide genotyping array 2019-04-17 30578877 Dahlin A 2018-12-19 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/30578877 Large-scale, multi-ethnic genome-wide association study identifies novel loci contributing to asthma susceptibility in adults. Adult asthma 611 African American cases, 1,915 African American controls 10,365 European ancestry cases, 16,110 European ancestry controls, cases and controls (see Moffatt et al 2010) Affymetrix [12660172] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007599 Genome-wide genotyping array 2019-04-17 30578877 Dahlin A 2018-12-19 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/30578877 Large-scale, multi-ethnic genome-wide association study identifies novel loci contributing to asthma susceptibility in adults. Adult asthma 1,300 Asian ancestry cases, 4,927 Asian ancestry controls 10,365 European ancestry cases, 16,110 European ancestry controls, cases and controls (see Moffatt et al 2010) Affymetrix [6389101] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007598 Genome-wide genotyping array 2019-04-17 30578877 Dahlin A 2018-12-19 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/30578877 Large-scale, multi-ethnic genome-wide association study identifies novel loci contributing to asthma susceptibility in adults. Adult asthma 1,320 Hispanic ancestry cases, 4,007 Hispanic ancestry controls 10,365 European ancestry cases, 16,110 European ancestry controls, cases and controls (see Moffatt et al 2010) Affymetrix [7735858] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007597 Genome-wide genotyping array 2019-09-23 31469255 Lule SA 2019-08-30 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/31469255 A genome-wide association and replication study of blood pressure in Ugandan early adolescents. Systolic blood pressure 815 African ancestry early adolescents NA Illumina [20074711] (imputed) 4 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST008749 Genome-wide genotyping array 2019-09-23 31469255 Lule SA 2019-08-30 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/31469255 A genome-wide association and replication study of blood pressure in Ugandan early adolescents. Diastolic blood pressure 815 African ancestry early adolescents NA Illumina [20074711] (imputed) 4 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST008750 Genome-wide genotyping array 2019-03-28 30586737 Sabater-Lleal M 2018-11-20 Circulation www.ncbi.nlm.nih.gov/pubmed/30586737 Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. Factor VIII levels 25,897 European ancestry individuals, 4,500 African American individuals, 773 Asian ancestry individuals, 1,440 Hispanic individuals NA Affymetrix, Illumina [13887196] (imputed) 66 factor VIII measurement http://www.ebi.ac.uk/efo/EFO_0004630 GCST007445 Genome-wide genotyping array 2019-03-28 30586737 Sabater-Lleal M 2018-11-20 Circulation www.ncbi.nlm.nih.gov/pubmed/30586737 Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. vWF levels 42,379 European ancestry individuals, 3,700 African American individuals, 275 Hispanic individuals NA Affymetrix, Illumina [10537485] (imputed) 87 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST007446 Genome-wide genotyping array 2019-03-28 30586737 Sabater-Lleal M 2018-11-20 Circulation www.ncbi.nlm.nih.gov/pubmed/30586737 Genome-Wide Association Trans-Ethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels. vWF and FVIII levels Up to 42,379 European ancestry individuals, up to 4,500 African American individuals, up to 773 Asian ancestry individuals, up to 1,440 Hispanic individuals NA Affymetrix, Illumina [up to 13887196] (imputed) 2 factor VIII measurement, von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0004629 GCST007447 Genome-wide genotyping array 2019-08-23 30584014 Huang M 2018-12-12 Neuroimage Clin www.ncbi.nlm.nih.gov/pubmed/30584014 Spatial correlations exploitation based on nonlocal voxel-wise GWAS for biomarker detection of AD. Voxel-wise structural brain imaging measurements in Alzheimer’s disease 708 European ancestry individuals NA Illumina [501584] 14 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST008491 Genome-wide genotyping array 2020-01-21 31518406 Abdellaoui A 2019-09-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31518406 Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness. Loneliness 511,280 European ancestry individuals NA Affymetrix, Illumina [up to 14113458] (imputed) 19 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST009463 Genome-wide genotyping array 2023-06-01 31518406 Abdellaoui A 2019-09-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31518406 Phenome-wide investigation of health outcomes associated with genetic predisposition to loneliness. Loneliness 490,689 European ancestry individuals NA Affymetrix, Illumina [7882378] (imputed) 0 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST013156 Genome-wide genotyping array 2019-10-09 31498392 Kusic DM 2019-09-09 Mil Med www.ncbi.nlm.nih.gov/pubmed/31498392 rs11670527 Upstream of ZNF264 Associated with Body Mass Index in the Coriell Personalized Medicine Collaborative. Body mass index 4,822 European ancestry individuals, 429 African American, Asian, Native Hawaiian/other Pacific Islander, Native American/Alaska native or unknown ancestry individuals NA Affymetrix [232536] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008823 Genome-wide genotyping array 2020-01-08 31504550 Bradfield JP 2019-07-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31504550 A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity. Childhood obesity 8,613 European ancestry cases, 3,213 African American cases, 69 Moroccan ancestry cases, 986 Hispanic/Latino cases, 124 East Asian ancestry cases, 12,696 European ancestry controls, 1,392 African American controls, 64 Moroccan ancestry controls, 993 Hispanic/Latino controls, 454 East Asian ancestry controls 921 European ancestry cases, 392 Southwest American Indian ancestry cases, 575 Hispanic cases, 1,930 European ancestry controls, 2,456 Southwest American Indian ancestry controls, 303 Hispanic controls Affymetrix, Illumina [up to 15123508] (imputed) 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST009383 Genome-wide genotyping array 2020-01-08 31504550 Bradfield JP 2019-07-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31504550 A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity. Childhood obesity 8,613 European ancestry cases, 3,213 African American cases, 69 Moroccan ancestry cases, 986 Hispanic/Latino cases, 124 East Asian ancestry cases, 12,696 European ancestry controls, 1,392 African American controls, 64 Moroccan ancestry controls, 993 Hispanic/Latino controls, 454 East Asian ancestry controls NA Affymetrix, Illumina [up to 15123508] (imputed) 57 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST009382 Genome-wide genotyping array 2019-09-04 31393916 Andaleon A 2019-08-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/31393916 Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. High density lipoprotein cholesterol levels 11,103 Hispanic or Latin American ancestry individuals NA Illumina [1770809] (imputed) 7 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008592 Genome-wide genotyping array 2019-09-04 31393916 Andaleon A 2019-08-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/31393916 Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. Triglyceride levels 11,103 Hispanic or Latin American ancestry individuals NA Illumina [1770809] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008591 Genome-wide genotyping array 2019-09-04 31393916 Andaleon A 2019-08-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/31393916 Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. Low density lipoprotein cholesterol levels 11,103 Hispanic or Latin American ancestry individuals NA Illumina [1770809] (imputed) 10 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008593 Genome-wide genotyping array 2019-09-04 31393916 Andaleon A 2019-08-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/31393916 Genetically regulated gene expression underlies lipid traits in Hispanic cohorts. Total cholesterol levels 11,103 Hispanic or Latin American ancestry individuals NA Illumina [1770809] (imputed) 12 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST008594 Genome-wide genotyping array 2019-09-20 30753327 Hishida A 2019-02-08 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/30753327 GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy. Anti-helicobacter pylori IgG seropositivity 1,239 Japanese ancestry cases, 2,146 Japanese ancestry controls 1,275 Japanese ancestry cases, 1,610 Japanese ancestry controls Illumina [575802] 0 Helicobacter pylori seropositivity http://www.ebi.ac.uk/efo/EFO_0009341 GCST008716 Genome-wide genotyping array 2019-09-20 30753327 Hishida A 2019-02-08 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/30753327 GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy. Severe gastric atrophy 120 Japanese ancestry cases, 760 Japanese ancestry controls 435 Japanese ancestry cases, 184 Japanese ancestry controls Illumina [575802] 1 atrophic gastritis http://www.ebi.ac.uk/efo/EFO_1000826 GCST008713 Genome-wide genotyping array 2019-09-20 30753327 Hishida A 2019-02-08 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/30753327 GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy. Pepsinogen-I levels 3,385 Japanese ancestry individuals 2,885 Japanese ancestry individuals Illumina [575802] 0 pepsinogen-I measurement http://www.ebi.ac.uk/efo/EFO_0010148 GCST008709 Genome-wide genotyping array 2019-09-20 30753327 Hishida A 2019-02-08 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/30753327 GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy. Pepsinogen I/II ratio 3,385 Japanese ancestry individuals 2,885 Japanese ancestry individuals Illumina [575802] 5 pepsinogen I/II ratio http://www.ebi.ac.uk/efo/EFO_0010149 GCST008712 Genome-wide genotyping array 2019-09-20 30753327 Hishida A 2019-02-08 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/30753327 GWAS analysis reveals a significant contribution of PSCA to the risk of Heliobacter pylori-induced gastric atrophy. Gastric atrophy 479 Japanese ancestry cases, 760 Japanese ancestry controls 1,091 Japanese ancestry cases, 184 Japanese ancestry controls Illumina [575802] 1 atrophic gastritis http://www.ebi.ac.uk/efo/EFO_1000826 GCST008714 Genome-wide genotyping array 2019-05-07 30586722 Aragam KG 2018-11-11 Circulation www.ncbi.nlm.nih.gov/pubmed/30586722 Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery. Heart failure 6,504 European ancestry cases, 387,652 European ancestry controls 4,042 European ancestry cases, 8,777 European ancestry controls NR [NR] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST007715 Genome-wide genotyping array 2019-05-07 30586722 Aragam KG 2018-11-11 Circulation www.ncbi.nlm.nih.gov/pubmed/30586722 Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery. Nonischemic cardiomyopathy 1,816 European ancestry cases, 388,326 European ancestry controls 3,282 European ancestry cases, 13,913 European ancestry controls NR [NR] 0 nonischemic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0009881 GCST007714 Genome-wide genotyping array 2020-01-13 31645637 Nagtegaal AP 2019-10-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31645637 Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment. Age-related hearing impairment (high minus low frequency) 9,675 European ancestry individuals 3,319 European ancestry individuals, 6,909 Hispanic individuals, 735 African American individuals Affymetrix, Illumina [NR] (imputed) 1 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST009431 Genome-wide genotyping array 2020-01-13 31645637 Nagtegaal AP 2019-10-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31645637 Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment. Age-related hearing impairment 9,675 European ancestry individuals 3,319 European ancestry individuals, 6,909 Hispanic individuals, 735 African American individuals Affymetrix, Illumina [NR] (imputed) 2 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST009430 Genome-wide genotyping array 2020-01-13 31645637 Nagtegaal AP 2019-10-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31645637 Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment. Age-related hearing impairment (low/mid frequency) 9,675 European ancestry individuals 3,319 European ancestry individuals, 6,909 Hispanic individuals, 735 African American individuals Affymetrix, Illumina [NR] (imputed) 6 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST009432 Genome-wide genotyping array 2020-01-13 31645637 Nagtegaal AP 2019-10-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31645637 Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment. Age-related hearing impairment (high frequency) 9,675 European ancestry individuals 3,319 European ancestry individuals, 6,909 Hispanic individuals, 735 African American individuals Affymetrix, Illumina [NR] (imputed) 6 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST009429 Genome-wide genotyping array 2019-11-19 29904099 Kottyan LC 2018-06-08 Genes Immun www.ncbi.nlm.nih.gov/pubmed/29904099 Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis. Eosinophilic esophagitis 1,210 European ancestry cases, 3,734 European ancestry controls NA Illumina [79405] 4 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST009070 Targeted genotyping array [ImmunoChip] 2020-01-09 31490055 Sun J 2019-09-06 Can J Surg www.ncbi.nlm.nih.gov/pubmed/31490055 A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and gene–environment interaction Cocaine use disorder 2,070 African American individuals, 1,570 European ancestry individuals 918 African American individuals, 1,382 European ancestry individuals Illumina [up to 47104916] (imputed) 4 cocaine use disorder http://www.ebi.ac.uk/efo/EFO_0010445 GCST009385 Genome-wide genotyping array 2020-01-09 31490055 Sun J 2019-09-06 Can J Surg www.ncbi.nlm.nih.gov/pubmed/31490055 A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and gene–environment interaction Cocaine use disorder x non-traditional parental care interaction 2,070 African American individuals, 1,570 European ancestry individuals 918 African American individuals, 1,382 European ancestry individuals Illumina [up to 47104916] (imputed) 1 cocaine use disorder, social environment measurement http://www.ebi.ac.uk/efo/EFO_0010445, http://www.ebi.ac.uk/efo/EFO_0010552 GCST009386 Genome-wide genotyping array 2020-01-09 31490055 Sun J 2019-09-06 Can J Surg www.ncbi.nlm.nih.gov/pubmed/31490055 A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and gene–environment interaction Cocaine use disorder x change in residence interaction 2,070 African American individuals, 1,570 European ancestry individuals 918 African American individuals, 1,382 European ancestry individuals Illumina [up to 47104916] (imputed) 3 cocaine use disorder, social environment measurement http://www.ebi.ac.uk/efo/EFO_0010445, http://www.ebi.ac.uk/efo/EFO_0010552 GCST009387 Genome-wide genotyping array 2020-01-09 31490055 Sun J 2019-09-06 Can J Surg www.ncbi.nlm.nih.gov/pubmed/31490055 A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and gene–environment interaction Cocaine use disorder x traumatic experience interaction 2,070 African American individuals, 1,570 European ancestry individuals 918 African American individuals, 1,382 European ancestry individuals Illumina [up to 47104916] (imputed) 0 cocaine use disorder, childhood trauma measurement http://www.ebi.ac.uk/efo/EFO_0010445, http://www.ebi.ac.uk/efo/EFO_0007979 GCST009388 Genome-wide genotyping array 2020-01-09 31490055 Sun J 2019-09-06 Can J Surg www.ncbi.nlm.nih.gov/pubmed/31490055 A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and gene–environment interaction Cocaine use disorder x household drinking and illicit drug use interaction 2,070 African American individuals, 1,570 European ancestry individuals 918 African American individuals, 1,382 European ancestry individuals Illumina [up to 47104916] (imputed) 0 cocaine use disorder, social environment measurement http://www.ebi.ac.uk/efo/EFO_0010445, http://www.ebi.ac.uk/efo/EFO_0010552 GCST009389 Genome-wide genotyping array 2020-01-09 31490055 Sun J 2019-09-06 Can J Surg www.ncbi.nlm.nih.gov/pubmed/31490055 A genome-wide association study of cocaine use disorder accounting for phenotypic heterogeneity and gene–environment interaction Cocaine use disorder x household tobacco use interaction 2,070 African American individuals, 1,570 European ancestry individuals 918 African American individuals, 1,382 European ancestry individuals Illumina [up to 47104916] (imputed) 2 cocaine use disorder, social environment measurement http://www.ebi.ac.uk/efo/EFO_0010445, http://www.ebi.ac.uk/efo/EFO_0010552 GCST009390 Genome-wide genotyping array 2019-12-11 31719529 Lyons PA 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719529 Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status. Eosinophilic granulomatosis with polyangiitis (MPO-ANCA positive) 159 European ancestry cases, 6,688 European ancestry controls 43 European and unknown ancestry cases, 121 European and unknown ancestry controls Affymetrix [9246221] (imputed) 2 Churg-Strauss syndrome http://www.ebi.ac.uk/efo/EFO_0007208 GCST009248 Genome-wide genotyping array 2019-12-11 31719529 Lyons PA 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719529 Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status. Eosinophilic granulomatosis with polyangiitis (ANCA negative) 352 European ancestry cases, 6,688 European ancestry controls 94 European and unknown ancestry cases, 121 European and unknown ancestry controls Affymetrix [9246221] (imputed) 2 Churg-Strauss syndrome http://www.ebi.ac.uk/efo/EFO_0007208 GCST009249 Genome-wide genotyping array 2019-12-11 31719529 Lyons PA 2019-11-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31719529 Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status. Eosinophilic granulomatosis with polyangiitis 534 European ancestry cases, 6,688 European ancestry controls 142 European and unknown ancestry cases, 121 European and unknown ancestry controls Affymetrix [9246221] (imputed) 4 Churg-Strauss syndrome http://www.ebi.ac.uk/efo/EFO_0007208 GCST009250 Genome-wide genotyping array 2020-02-05 31919418 Shah S 2020-01-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31919418 Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure. Heart failure 47,309 European ancestry cases, 930,014 European ancestry controls NA Affymetrix, Illumina [8246881] (imputed) 12 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST009541 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Metabolic syndrome 1,362 Korean ancestry cases, 6,061 Korean ancestry controls NA Affymetrix [at least 584061] (imputed) 1 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST009663 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Hypertriglyceridemia 7,423 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 18 Hypertriglyceridemia http://www.ebi.ac.uk/efo/EFO_0004211 GCST009662 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Low HDL-cholesterol levels 7,423 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 17 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009661 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Low HDL-cholesterol levels 2,253 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009656 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. High fasting blood glucose 2,253 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST009655 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Hypertension 2,253 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST009654 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. High fasting blood glucose 7,423 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST009660 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Hypertension 7,423 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST009659 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Metabolic syndrome 502 Korean ancestry cases, 1,751 Korean ancestry controls NA Affymetrix [at least 584061] (imputed) 0 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST009658 Genome-wide genotyping array 2020-02-19 31910446 Oh SW 2020-01-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/31910446 Genome-wide association study of metabolic syndrome in Korean populations. Hypertriglyceridemia 2,253 Korean ancestry cases and controls NA Affymetrix [at least 584061] (imputed) 2 Hypertriglyceridemia http://www.ebi.ac.uk/efo/EFO_0004211 GCST009657 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_74 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011411 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_8 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011412 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_80 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011413 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_82 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011414 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_86 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011415 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_9 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011416 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_95 (Cytophagales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011417 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_97 (Clostridiales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011418 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_1 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011419 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_106 (Barnesiella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011420 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_108 (Cytophagales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011421 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_11 (Parabacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011422 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_110 (Clostridiales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011423 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_116 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011424 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_12 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011425 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_120 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011426 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_121 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011427 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_123 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011428 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_124 (Paraprevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011429 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_13 (Subdoligranulum) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011430 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_132 (Bacteroidales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011431 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_137 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011432 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_140 (Desulfovibrio) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011433 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_150 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011434 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_155 (Butyrivibrio) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 19 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011435 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_157 (Barnesiella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011436 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_16 (Faecalibacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011437 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_166 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011438 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_17 (Parabacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011439 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_171 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011440 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_19 (Bacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011441 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_197 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011442 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_2 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011443 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_21 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011444 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_211 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011445 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_23 (Faecalibacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011446 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_24 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011447 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_26 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011448 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_271 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011449 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_298 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011450 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_3 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011451 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_30 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011452 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_100 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011355 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_101 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011356 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_102 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011357 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_105 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011358 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_106 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011359 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_108 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011360 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_109 (Paraprevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011361 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_11 (Parabacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011362 Genome-wide genotyping array 2020-04-17 31903573 van Reij RRI 2020-01-01 Anaesthesia www.ncbi.nlm.nih.gov/pubmed/31903573 The association between genome-wide polymorphisms and chronic postoperative pain: a prospective observational study. Chronic postoperative pain 34 European ancestry cases, 269 European ancestry controls 11 European ancestry cases, 39 European ancestry controls Illumina [6293655] (imputed) 2 chronic post-operative pain measurement http://www.ebi.ac.uk/efo/EFO_0010640 GCST009839 Genome-wide genotyping array 2020-01-08 30297969 Mahajan A 2018-10-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30297969 Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Type 2 diabetes (adjusted for BMI) 50,409 European ancestry cases, 523,897 European ancestry controls NA Affymetrix, Illumina [~ 27000000] (imputed) 17 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST009380 Genome-wide genotyping array 2020-01-08 30297969 Mahajan A 2018-10-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30297969 Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Type 2 diabetes 74,124 European ancestry cases, 824,006 European ancestry controls NA Affymetrix, Illumina [~ 27000000] (imputed) 383 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST009379 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Acidaminococcaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011309 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Bacteroidaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011310 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Coriobacteriaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011311 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Erysipelotrichaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011312 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Lachnospiraceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011313 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Porphyromonadaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011314 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Prevotellaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011315 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Rikenellaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011316 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Ruminococcaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 19 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011317 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Sutterellaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011318 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Alistipes abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011319 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Alloprevotella abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011320 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Alphaproteobacteria abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011321 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Bacteroidales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011322 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Bacteroides abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011323 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Bacteroidetes abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011324 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Barnesiella abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011325 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_19 (Bacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011380 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_2 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011381 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_21 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011382 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_23 (Faecalibacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011383 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_235 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011384 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_24 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011385 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_257 (Mitsuokella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011386 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_26 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011387 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_113 (Bacteroidales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011363 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_117 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011364 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_119 (Desulfovibrio) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011365 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_12 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011366 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_126 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011367 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_13 (Subdoligranulum) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011368 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_130 (Butyrivibrio) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011369 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_137 (Catenibacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011370 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_138 (Oscillibacter) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011371 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_140 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011372 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_15 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011373 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_150 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011374 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_16 (Faecalibacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011375 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_163 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011376 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_165 (Porphyromonadaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011377 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_17 (Parabacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011378 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_173 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011379 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Actinobacteria abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011301 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Alphaproteobacteria abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011302 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Bacteroidia abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011303 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Betaproteobacteria abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011304 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Clostridia abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 21 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011305 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Erysipelotrichia abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011306 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Gammaproteobacteria abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011307 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Negativicutes abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011308 Genome-wide genotyping array 2020-05-19 31926482 Shen H 2020-01-11 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/31926482 Polygenic prediction and GWAS of depression, PTSD, and suicidal ideation/self-harm in a Peruvian cohort. Depression 1,076 Peruvian cases, 2,328 Peruvian controls NA NR [NR] 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST009978 Genome-wide genotyping array 2020-05-19 31926482 Shen H 2020-01-11 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/31926482 Polygenic prediction and GWAS of depression, PTSD, and suicidal ideation/self-harm in a Peruvian cohort. Post-traumatic stress disorder 1,698 Peruvian cases, 1,716 Peruvian controls NA NR [3389129] (imputed) 4 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST009977 Genome-wide genotyping array 2020-05-19 31926482 Shen H 2020-01-11 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/31926482 Polygenic prediction and GWAS of depression, PTSD, and suicidal ideation/self-harm in a Peruvian cohort. Suicidal or self-harm ideation 522 Peruvian cases, 2,882 Peruvian controls NA NR [NR] 9 suicidal ideation http://www.ebi.ac.uk/efo/EFO_0004320 GCST009976 Genome-wide genotyping array 2021-06-02 31913414 Bahrami S 2020-01-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31913414 Shared Genetic Loci Between Body Mass Index and Major Psychiatric Disorders: A Genome-wide Association Study. Major psychiatric disorders or BMI (pleiotropy) at least 34,241 schizophrenia cases, 20,352 bipolar disorder cases, up to 135,458 major depression cases, 795,640 individuals with BMI measurements, 421,863 controls NA NR [NR] 0 unipolar depression, bipolar disorder, schizophrenia, body mass index http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0004340 GCST011777 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_35 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011455 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_39 (Alphaproteobacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011456 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_4 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011457 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_40 (Proteobacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011458 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_45 (Faecalibacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011459 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_47 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011460 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_5 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011461 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_53 (Aestuariispira) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011462 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_54 (Holdemanella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011463 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_55 (Barnesiella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011464 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_558 (Bacteroidales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011465 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_58 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011466 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_59 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011467 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_6 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011468 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_62 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011469 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Catenibacterium abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011326 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Clostridiales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011327 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Clostridium_XlVa abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011328 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Coprococcus abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011329 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Faecalibacterium abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011330 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Firmicutes abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011331 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Holdemanella abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011332 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Lachnospiraceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011333 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Oscillibacter abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011334 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Parabacteroides abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011335 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Paraprevotella abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011336 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Parasutterella abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011337 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Phascolarctobacterium abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011338 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Porphyromonadaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011339 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Prevotella abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011340 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Prevotellaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011341 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Roseburia abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011342 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Ruminococcaceae abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011343 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Ruminococcus abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011344 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Ruminococcus2 abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011345 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Subdoligranulum abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011346 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Sutterella abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011347 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. O_Bacteroidales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011348 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. O_Burkholderiales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011349 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. O_Clostridiales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011350 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. O_Coriobacteriales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011351 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. O_Erysipelotrichales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011352 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. O_Selenomonadales abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011353 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_1 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011354 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_166 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 19 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011639 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_17 (Parabacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011640 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_171 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011641 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_19 (Bacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011642 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_197 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011643 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_2 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011644 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_27 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011388 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_277 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011389 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_3 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011390 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_30 (Roseburia) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011391 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_31 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011392 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_33 (Holdemanella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011393 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_34 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011394 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_354 (Alloprevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011395 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_38 (Alphaproteobacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011396 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_39 (Proteobacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011397 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_4 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011398 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_46 (Lachnospiraceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011399 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_5 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011400 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_50 (Aestuariispira) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011401 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_51 (Barnesiella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011402 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_53 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011403 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_56 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011404 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_58 (Sutterellaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011405 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_6 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011406 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_65 (Parabacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011407 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_69 (Clostridiales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011408 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_7 (Lachnospiraceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011409 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_73 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011410 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_32 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011453 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_34 (Holdemanella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011454 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_21 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011645 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_211 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 20 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011646 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_23 (Faecalibacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011647 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_24 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011648 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_26 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011649 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_271 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011650 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_298 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011651 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_3 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011652 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_30 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011653 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_32 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011654 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_34 (Holdemanella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011655 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_35 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011656 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_39 (Alphaproteobacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011657 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_4 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011658 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_40 (Proteobacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011659 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_45 (Faecalibacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011660 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_47 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 24 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011661 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_5 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011662 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_53 (Aestuariispira) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011663 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_54 (Holdemanella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011664 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_55 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011665 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_558 (Bacteroidales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011666 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_58 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011667 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_59 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011668 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_6 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011669 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_21 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011695 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_22 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011696 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_23 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011697 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_24 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011698 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_25 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011699 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_26 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011700 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_27 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011701 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_28 (Holdemanella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011702 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_29 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011703 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_3 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011704 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_30 (Paraprevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011705 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_31 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011706 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_32 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011707 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_33 (Paraprevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011708 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_34 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011709 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_35 (Alphaproteobacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011710 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_36 (Aestuariispira) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011711 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_37 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011712 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_38 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011713 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_39 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 20 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011714 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_4 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011715 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_40 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011716 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_65 (Sutterellaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011470 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_7 (Lachnospiraceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011471 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_72 (Parabacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011472 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_62 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011670 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_65 (Sutterellaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011671 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_7 (Lachnospiraceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011672 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_72 (Parabacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011673 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_78 (Clostridiales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011674 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_8 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011675 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_84 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011676 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_85 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011677 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_9 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011678 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_92 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011679 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_94 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011680 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_98 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011681 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_1 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011682 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_10 (Parabacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011683 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_11 (Lachnospiraceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011684 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_12 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011685 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_13 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011686 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_14 (Lachnospiraceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011687 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_15 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011688 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_16 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 20 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011689 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_17 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011690 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_18 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011691 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_19 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011692 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_2 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011693 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_20 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011694 Genome-wide genotyping array 2020-03-05 31959995 Schlosser P 2020-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31959995 Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans. Urinary metabolite modules (eigenmetabolites) in chronic kidney disease 1,221 cases 406 cases Illumina [7750367] (imputed) 46 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST009735 Genome-wide genotyping array 2020-03-03 31959995 Schlosser P 2020-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31959995 Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans. Urinary metabolite levels in chronic kidney disease 1,221 cases 406 cases Illumina [7750367] (imputed) 240 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST009733 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_21 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011498 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_22 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011499 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_23 (Barnesiella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011500 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_24 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011501 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_25 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011502 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_26 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 20 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011503 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_27 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011504 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_28 (Holdemanella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011505 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_29 (Barnesiella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011506 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_3 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011507 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_30 (Paraprevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011508 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_31 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011509 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_32 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 20 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011510 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_33 (Paraprevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011511 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_34 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011512 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_35 (Alphaproteobacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011513 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_36 (Aestuariispira) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011514 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_37 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011515 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_38 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011516 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_39 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011517 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_4 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011518 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_41 (Barnesiella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011519 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_42 (Alphaproteobacteria) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011520 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_43 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011521 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_44 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011522 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_45 (Clostridiales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011523 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_46 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011524 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_47 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011525 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_48 (Sutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011526 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_49 (Parasutterella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011527 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_5 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011528 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_6 (Subdoligranulum) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011529 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_7 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011530 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_8 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011531 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_9 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011532 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Alphaproteobacteria prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011533 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. C_Negativicutes prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011534 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Acidaminococcaceae prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011535 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. F_Prevotellaceae prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011536 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Alloprevotella prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011537 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Alphaproteobacteria prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011538 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Bacteroidales prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011539 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Bacteroidetes prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011540 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Barnesiella prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011541 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Catenibacterium prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011542 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Coprococcus prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011543 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Holdemanella prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011544 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Parabacteroides prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011545 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Paraprevotella prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011546 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Parasutterella prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011547 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_78 (Clostridiales) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011473 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_8 (Ruminococcaceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011474 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_84 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011475 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_85 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011476 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_9 (Alistipes) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011477 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_92 (Ruminococcus) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011478 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_94 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011479 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_98 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011480 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. P_Actinobacteria abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011481 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. P_Bacteroidetes abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011482 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. P_Firmicutes abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011483 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. P_Proteobacteria abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011484 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_1 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011485 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_10 (Parabacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011486 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_11 (Lachnospiraceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011487 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_12 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011488 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_13 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011489 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_14 (Lachnospiraceae) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011490 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_15 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011491 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_16 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011492 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_17 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011493 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_18 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011494 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_19 (Prevotella) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011495 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_2 (Bacteroides) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011496 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_20 (Phascolarctobacterium) abundance 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011497 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Phascolarctobacterium prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011548 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Porphyromonadaceae prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011549 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Prevotella prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011550 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Prevotellaceae prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011551 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Ruminococcus prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011552 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. G_Sutterella prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011553 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. O_Selenomonadales prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011554 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_1 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011555 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_100 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011556 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_101 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011557 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_102 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011558 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_105 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011559 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_106 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011560 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_108 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011561 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_109 (Paraprevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011562 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_11 (Parabacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011563 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_113 (Bacteroidales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011564 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_117 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011565 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_119 (Desulfovibrio) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011566 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_12 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011567 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_126 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011568 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_13 (Subdoligranulum) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011569 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_130 (Butyrivibrio) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011570 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_137 (Catenibacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011571 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_138 (Oscillibacter) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011572 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_140 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011573 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_15 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011574 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_150 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011575 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_16 (Faecalibacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011576 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_163 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011577 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_165 (Porphyromonadaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011578 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_17 (Parabacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011579 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_173 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 19 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011580 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_19 (Bacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011581 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_2 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011582 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_21 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011583 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_23 (Faecalibacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011584 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_235 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011585 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_24 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011586 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_257 (Mitsuokella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011587 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_26 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011588 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_27 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011589 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_277 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011590 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_3 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011591 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_30 (Roseburia) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011592 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_31 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011593 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_33 (Holdemanella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011594 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_34 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011595 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_354 (Alloprevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011596 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_38 (Alphaproteobacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011597 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_11 (Parabacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011623 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_110 (Clostridiales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011624 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_116 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011625 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_12 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011626 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_120 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011627 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_121 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011628 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_123 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011629 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_124 (Paraprevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011630 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_13 (Subdoligranulum) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011631 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_132 (Bacteroidales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011632 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_137 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011633 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_140 (Desulfovibrio) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011634 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_150 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011635 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_155 (Butyrivibrio) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011636 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_157 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011637 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_16 (Faecalibacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011638 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_41 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011717 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_42 (Alphaproteobacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011718 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_43 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011719 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_44 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011720 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_45 (Clostridiales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011721 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_46 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011722 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_47 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011723 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_48 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011724 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_49 (Parasutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011725 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_39 (Proteobacteria) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011598 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_4 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011599 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_46 (Lachnospiraceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011600 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_5 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011601 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_50 (Aestuariispira) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011602 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_51 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011603 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_53 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011604 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_56 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011605 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_58 (Sutterellaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011606 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_6 (Sutterella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011607 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_65 (Parabacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011608 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_69 (Clostridiales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011609 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_7 (Lachnospiraceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011610 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_73 (Prevotella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011611 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_74 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011612 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_8 (Ruminococcaceae) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011613 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_80 (Ruminococcus) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011614 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_82 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011615 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_86 (Phascolarctobacterium) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011616 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_9 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011617 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_95 (Cytophagales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011618 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU97_97 (Clostridiales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011619 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_1 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011620 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_106 (Barnesiella) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011621 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. OTU99_108 (Cytophagales) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011622 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_5 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011726 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_6 (Subdoligranulum) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011727 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_7 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011728 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_8 (Bacteroides) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011729 Genome-wide genotyping array 2022-07-04 33462482 Ruhlemann MC 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462482 Genome-wide association study in 8,956 German individuals identifies influence of ABO histo-blood groups on gut microbiome. TestASV_9 (Alistipes) prevalence 8,956 German ancestry individuals NA NR [6900000] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90011730 Genome-wide genotyping array 2020-01-28 31670792 Ghorbani Mojarrad N 2019-10-31 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31670792 Association Between Polygenic Risk Score and Risk of Myopia. Refractive error (age-at-onset of spectacle wearing-inferred) 287,448 European ancestry individuals NA NR [~ 1100000] 0 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST009520 Genome-wide genotyping array 2020-01-28 31670792 Ghorbani Mojarrad N 2019-10-31 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31670792 Association Between Polygenic Risk Score and Risk of Myopia. Refractive error (autorefraction measured) 95,619 European ancestry individuals NA NR [~ 1100000] 0 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST009521 Genome-wide genotyping array 2020-01-07 31754094 Pisanu C 2019-11-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31754094 Evidence that genes involved in hedgehog signaling are associated with both bipolar disorder and high BMI. Bipolar disorder or body mass index 20,352 European ancestry bipolar disorder cases, 31,358 European ancestry controls, 322,154 European ancestry individuals with BMI data. NA Illumina [2013566] (imputed) 13 bipolar disorder, body mass index http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0004340 GCST009371 Genome-wide genotyping array, Targeted genotyping array 2020-01-07 31754094 Pisanu C 2019-11-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31754094 Evidence that genes involved in hedgehog signaling are associated with both bipolar disorder and high BMI. Bipolar disorder or type 2 diabetes 20,352 European ancestry bipolar disorder cases, 26,676 European ancestry type 2 diabetes cases, 163,890 European ancestry controls NA NR [2013566] (imputed) 2 bipolar disorder, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005148 GCST009372 Genome-wide genotyping array 2020-03-11 29381148 Gong J 2017-12-21 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/29381148 Trans-ethnic analysis of metabochip data identifies two new loci associated with BMI. Body mass index 35,606 African American individuals, 26,048 Hispanic/Latino individuals, 22,466 Asian or Native Hawaiian ancestry individuals, 17,859 European ancestry individuals, 535 Native American individuals NA Illumina [at least 200000] 27 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009764 Targeted genotyping array [Metabochip] 2020-10-15 32080893 Divers J 2020-02-20 Clin Transplant www.ncbi.nlm.nih.gov/pubmed/32080893 GWAS for time to failure of kidney transplants from African American deceased donors. Graft survival time in renal transplantation (donor effect) 532 African American donors 250 African American donors Illumina [> 13000000] (imputed) 4 renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST010683 Genome-wide genotyping array 2020-10-15 32080893 Divers J 2020-02-20 Clin Transplant www.ncbi.nlm.nih.gov/pubmed/32080893 GWAS for time to failure of kidney transplants from African American deceased donors. Graft survival time in renal transplantation (donor effect) x APOL1 genotype interaction 532 African American donors 250 African American donors Illumina [> 13000000] (imputed) 6 renal transplant outcome measurement, APOL1 risk genotype carrier status, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0009324, http://www.ebi.ac.uk/efo/EFO_0007892 GCST010682 Genome-wide genotyping array 2020-06-16 31904872 Chou WC 2020-01-06 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31904872 A Functional Variant Near XCL1 Gene Improves Breast Cancer Survival via Promoting Cancer Immunity. Survival in breast cancer (estrogen-receptor positive) 953 Taiwanese individuals NA Affymetrix [632566] (imputed) 4 survival time http://www.ebi.ac.uk/efo/EFO_0000714 GCST010079 Genome-wide genotyping array 2020-02-21 31869403 Kowalski MH 2019-12-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31869403 Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. Hematocrit 14,735 African American individuals, 6,762 African ancestry individuals, 21,684 Hispanic/Latino individuals 7,050 African American individuals Affymetrix, Illumina [up to 35800000] (imputed) 5 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST009682 Genome-wide genotyping array 2020-02-21 31869403 Kowalski MH 2019-12-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31869403 Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. Hemoglobin levels 14,739 African American individuals, 6,762 African ancestry individuals, 21,686 Hispanic/Latino individuals 7,037 African American individuals Affymetrix, Illumina [up to 35800000] (imputed) 10 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST009681 Genome-wide genotyping array 2020-02-21 31869403 Kowalski MH 2019-12-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31869403 Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations. White blood cell count 14,743 African American individuals, 6,762 African ancestry individuals, 21,034 Hispanic/Latino individuals 6,743 African American individuals Affymetrix, Illumina [up to 35800000] (imputed) 6 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST009683 Genome-wide genotyping array 2020-04-15 32066696 Dalvie S 2020-01-27 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066696 Genomic influences on self-reported childhood maltreatment. Childhood maltreatment 124,711 European ancestry individuals 26,290 European ancestry individuals Affymetrix, Illumina [at least 800000] (imputed) 3 childhood trauma measurement http://www.ebi.ac.uk/efo/EFO_0007979 GCST009816 Genome-wide genotyping array 2019-11-26 31676865 Klarin D 2019-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31676865 Genome-wide association analysis of venous thromboembolism identifies new risk loci and genetic overlap with arterial vascular disease. Venous thromboembolism 23,151 European ancestry cases, 553,439 European ancestry controls, 2,261 African American cases, 49,400 African American controls, 654 Hispanic cases, 21,214 Hispanic controls 17,672 cases, 167,295 controls Affymetrix [up to 34000000] (imputed) 18 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST009097 Genome-wide genotyping array 2021-03-22 31902292 Kanipakam H 2020-01-17 J Biomol Struct Dyn www.ncbi.nlm.nih.gov/pubmed/31902292 Structural and functional alterations of nitric oxide synthase 3 due to missense variants associate with high-altitude pulmonary edema through dynamic study. High-altitude pulmonary edema 96 Indo-Aryan ancestry cases, 96 Indo-Aryan ancestry controls 200 cases, 200 controls Illumina [NR] 0 high altitude pulmonary edema http://www.ebi.ac.uk/efo/EFO_1002002 GCST011375 Genome-wide genotyping array 2018-07-02 29603369 Naito T 2018-03-30 J Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29603369 Clinical and genetic risk factors for decreased bone mineral density in Japanese patients with inflammatory bowel disease. Bone mineral density (lumbar spine) in inflammatory bowel disease 254 Japanese ancestry cases NA Affymetrix [4384682] (imputed) 4 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST005783 Genome-wide genotyping array 2018-07-02 29603369 Naito T 2018-03-30 J Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/29603369 Clinical and genetic risk factors for decreased bone mineral density in Japanese patients with inflammatory bowel disease. Bone mineral density (femoral neck) in inflammatory bowel disease 254 Japanese ancestry cases NA Affymetrix [4384682] (imputed) 7 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST005784 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Triacylglycerol 56:6 levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 10 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008862 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Malate levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 4 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST008863 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Niacinamide levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 2 niacinamide measurement http://www.ebi.ac.uk/efo/EFO_0010511 GCST008864 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Sphingomyelin 24:0 levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 6 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST008865 Genome-wide genotyping array 2019-10-21 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Uridine levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 2 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST008894 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Triacylglycerol 56:2 levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008866 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Tyrosine levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 7 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST008867 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Xanthine levels 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 2 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST008868 Genome-wide genotyping array 2019-10-17 31560688 Geidenstam N 2019-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/31560688 Using metabolite profiling to construct and validate a metabolite risk score for predicting future weight gain. Metabolite risk score for predicting weight gain 1,937 individuals NA Affymetrix, Illumina [up to 22000000] (imputed) 7 metabolite measurement, body weight gain http://www.ebi.ac.uk/efo/EFO_0004725, http://www.ebi.ac.uk/efo/EFO_0004566 GCST008869 Genome-wide genotyping array 2019-02-26 30470734 Hackinger S 2018-11-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30470734 Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. Schizophrenia 924 Greek ancestry cases, 1,125 Greek ancestry controls NA Illumina [14528340] (imputed) 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST007219 Genome-wide genotyping array 2019-02-26 30470734 Hackinger S 2018-11-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30470734 Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. Type 2 diabetes 822 Greek ancestry cases, 1,125 Greek ancestry controls NA Illumina [14528340] (imputed) 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007221 Genome-wide genotyping array 2019-02-26 30470734 Hackinger S 2018-11-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30470734 Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. Schizophrenia vs type 2 diabetes 924 Greek ancestry schizophrenia cases, 822 Greek ancestry T2D cases NA Illumina [14528340] (imputed) 1 schizophrenia, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005148 GCST007223 Genome-wide genotyping array 2019-02-26 30470734 Hackinger S 2018-11-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30470734 Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. Type 2 diabetes vs schizophrenia and type 2 diabetes 505 Greek ancestry schizophrenia and T2D cases, 822 Greek ancestry T2D cases NA Illumina [14528340] (imputed) 0 schizophrenia, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005148 GCST007224 Genome-wide genotyping array 2019-02-26 30470734 Hackinger S 2018-11-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30470734 Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. Schizophrenia and type 2 diabetes 505 Greek ancestry cases, 1,125 Greek ancestry controls NA Illumina [14528340] (imputed) 2 schizophrenia, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005148 GCST007220 Genome-wide genotyping array 2019-02-26 30470734 Hackinger S 2018-11-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30470734 Evidence for genetic contribution to the increased risk of type 2 diabetes in schizophrenia. Schizophrenia vs schizophrenia and type 2 diabetes 505 Greek ancestry schizophrenia and T2D cases, 924 Greek ancestry schizophrenia cases NA Illumina [14528340] (imputed) 0 schizophrenia, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005148 GCST007222 Genome-wide genotyping array 2019-04-30 30468137 Fabbri C 2018-11-23 Br J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30468137 Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples. Treatment resistant depression 1,378 European ancestry treatment resistant cases, 934 European ancestry responders to first treatment, 914 European ancestry non-responders to first treatment NA Affymetrix, Illumina [7000000] (imputed) 8 treatment resistant depression, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0009854, http://purl.obolibrary.org/obo/GO_0036276 GCST007665 Genome-wide genotyping array 2019-04-30 30468137 Fabbri C 2018-11-23 Br J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30468137 Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples. Treatment resistant depression 1,378 European ancestry treatment resistant cases, 934 European ancestry responders to first treatment NA Affymetrix, Illumina [7000000] (imputed) 7 treatment resistant depression, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0009854, http://purl.obolibrary.org/obo/GO_0036276 GCST007667 Genome-wide genotyping array 2019-04-30 30468137 Fabbri C 2018-11-23 Br J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30468137 Genome-wide association study of treatment-resistance in depression and meta-analysis of three independent samples. Depressive symptom improvement 1,378 European ancestry treatment resistant cases, 934 European ancestry responders to first treatment NA Affymetrix, Illumina [7000000] (imputed) 16 depressive symptom measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007006, http://purl.obolibrary.org/obo/GO_0036276 GCST007666 Genome-wide genotyping array 2019-07-15 30252935 Smith AH 2018-09-25 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30252935 Risk locus identification ties alcohol withdrawal symptoms to SORCS2. Alcohol withdrawal symptoms 1,231 African American individuals NA Illumina [NR] (imputed) 0 alcohol withdrawal http://www.ebi.ac.uk/efo/EFO_0004777 GCST008136 Genome-wide genotyping array 2019-07-15 30252935 Smith AH 2018-09-25 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30252935 Risk locus identification ties alcohol withdrawal symptoms to SORCS2. Alcohol withdrawal symptoms 1,297 European American individuals 181 European American individuals Illumina [NR] (imputed) 1 alcohol withdrawal http://www.ebi.ac.uk/efo/EFO_0004777 GCST008137 Genome-wide genotyping array 2019-05-07 30610941 Wang AW 2019-01-02 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30610941 Genome-wide association study in two populations to determine genetic variants associated with Toxoplasma gondii infection and relationship to schizophrenia risk. Anti-Toxoplasma gondii IgG seropositivity 256 Ashkenazi Jewish cases, 68 African American cases, 534 Ashkenazi Jewish controls, 217 African American controls NA Affymetrix, Illumina [up to 1101633] (imputed) 4 Toxoplasma gondii seropositivity http://www.ebi.ac.uk/efo/EFO_0007047 GCST007726 Genome-wide genotyping array 2019-08-19 31268507 Periyasamy S 2019-07-03 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31268507 Association of Schizophrenia Risk With Disordered Niacin Metabolism in an Indian Genome-wide Association Study. Schizophrenia 816 Indian ancestry cases, 900 Indian ancestry controls, 505 Indian ancestry cases and 871 Indian ancestry controls from 405 families, up to 36,989 European and unknown ancestry cases, up to 113,075 European and unknown ancestry controls NA Illumina [up to 5582932] (imputed) 101 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST008459 Genome-wide genotyping array 2021-04-28 32939015 Zhu Z 2020-09-16 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32939015 A genome-wide association study reveals a substantial genetic basis underlying the Ebbinghaus illusion. Ebbinghaus illusion (underestimation) 1,986 Chinese ancestry individuals 839 Chinese ancestry individuals Illumina [at least 830937] (imputed) 36 visual perception measurement http://www.ebi.ac.uk/efo/EFO_0009700 GCST011567 Genome-wide genotyping array 2021-04-28 32939015 Zhu Z 2020-09-16 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32939015 A genome-wide association study reveals a substantial genetic basis underlying the Ebbinghaus illusion. Ebbinghaus illusion (overestimation) 1,986 Chinese ancestry individuals 839 Chinese ancestry individuals Illumina [at least 830937] (imputed) 182 visual perception measurement http://www.ebi.ac.uk/efo/EFO_0009700 GCST011568 Genome-wide genotyping array 2019-12-10 31679650 Nath AP 2019-10-30 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31679650 Multivariate Genome-Wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy. Cytokine levels 9,263 Finnish ancestry individuals NA Illumina [6022229] (imputed) 10 interferon gamma measurement, platelet-derived growth factor BB measurement, interleukin 4 measurement, interleukin 10 measurement, stromal cell-derived factor 1 alpha measurement, interleukin-6 measurement, interleukin 12 measurement, interleukin 17 measurement, vascular endothelial growth factor measurement, fibroblast growth factor basic measurement, granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008165, http://www.ebi.ac.uk/efo/EFO_0008264, http://www.ebi.ac.uk/efo/EFO_0008184, http://www.ebi.ac.uk/efo/EFO_0004750, http://www.ebi.ac.uk/efo/EFO_0008293, http://www.ebi.ac.uk/efo/EFO_0004810, http://www.ebi.ac.uk/efo/EFO_0004753, http://www.ebi.ac.uk/efo/EFO_0008174, http://www.ebi.ac.uk/efo/EFO_0004762, http://www.ebi.ac.uk/efo/EFO_0008130, http://www.ebi.ac.uk/efo/EFO_0008142 GCST009243 Genome-wide genotyping array 2019-12-10 31679650 Nath AP 2019-10-30 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31679650 Multivariate Genome-Wide Association Analysis of a Cytokine Network Reveals Variants with Widespread Immune, Haematological, and Cardiometabolic Pleiotropy. Cytokine network levels (multivariate analysis) 9,263 Finnish ancestry individuals NA Illumina [6022229] (imputed) 13 interferon gamma measurement, platelet-derived growth factor BB measurement, interleukin 4 measurement, interleukin 10 measurement, stromal cell-derived factor 1 alpha measurement, interleukin-6 measurement, interleukin 12 measurement, interleukin 17 measurement, vascular endothelial growth factor measurement, fibroblast growth factor basic measurement, granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008165, http://www.ebi.ac.uk/efo/EFO_0008264, http://www.ebi.ac.uk/efo/EFO_0008184, http://www.ebi.ac.uk/efo/EFO_0004750, http://www.ebi.ac.uk/efo/EFO_0008293, http://www.ebi.ac.uk/efo/EFO_0004810, http://www.ebi.ac.uk/efo/EFO_0004753, http://www.ebi.ac.uk/efo/EFO_0008174, http://www.ebi.ac.uk/efo/EFO_0004762, http://www.ebi.ac.uk/efo/EFO_0008130, http://www.ebi.ac.uk/efo/EFO_0008142 GCST009244 Genome-wide genotyping array 2019-01-25 30583798 Bovijn J 2018-12-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30583798 GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology. Erectile dysfunction 6,175 European ancestry male cases, 217,630 European ancestry male controls NA Affymetrix, Illumina [at least 807411] (imputed) 23 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST006956 Genome-wide genotyping array 2021-03-18 31482590 Joyner C 2019-09-04 Biom J www.ncbi.nlm.nih.gov/pubmed/31482590 A two-phase Bayesian methodology for the analysis of binary phenotypes in genome-wide association studies. Colorectal cancer 84 South East Asian ancestry cases, 89 South East Asian ancestry controls NA NR [495532] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST011298 Genome-wide genotyping array 2019-10-17 31562322 Takata R 2019-09-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31562322 12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population. Prostate cancer 5,088 Japanese ancestry cases, 10,682 Japanese ancestry controls 4,818 Japanese ancestry cases, 73,261 Japanese ancestry controls Illumina [7742602] (imputed) 37 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST008860 Genome-wide genotyping array 2020-07-08 32066700 Zhang R 2020-02-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066700 Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls. Serum immune biomarker levels 184 Scandinavian ancestry bipolar disorder cases, 107 Scandinavian ancestry controls NA Affymetrix, Illumina [> 5000000] (imputed) 46 inflammatory biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004872 GCST010146 Genome-wide genotyping array 2020-07-08 32066700 Zhang R 2020-02-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066700 Genome-wide study of immune biomarkers in cerebrospinal fluid and serum from patients with bipolar disorder and controls. Cerebrospinal fluid immune biomarker levels 114 Scandinavian ancestry bipolar disorder cases, 83 Scandinavian ancestry controls NA Affymetrix, Illumina [> 5600000] (imputed) 15 cerebrospinal fluid biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006794 GCST010145 Genome-wide genotyping array 2020-11-24 31362389 Chen YC 2019-07-29 J Clin Med www.ncbi.nlm.nih.gov/pubmed/31362389 LRRTM4 and PCSK5 Genetic Polymorphisms as Markers for Cognitive Impairment in A Hypotensive Aging Population: A Genome-Wide Association Study in Taiwan. Hypotension and cognitive impairment 56 Han Chinese ancestry cases, 1,799 Han Chinese ancestry controls NA NR [590244] 3 hypotension, Cognitive impairment http://www.ebi.ac.uk/efo/EFO_0005251, http://purl.obolibrary.org/obo/HP_0100543 GCST010762 Genome-wide genotyping array 2019-10-30 30976013 Dekker AM 2019-04-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30976013 Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 4,244 European ancestry cases, 3,106 European ancestry controls NA Illumina [233331] 1 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST008978 Exome genotyping array [Exome array] 2019-09-16 31482140 Meng W 2019-08-28 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31482140 Genome-wide association study of knee pain identifies associations with GDF5 and COL27A1 in UK Biobank. Knee pain 22,204 British ancestry cases, 149,312 British ancestry controls NA Affymetrix [15377520] (imputed) 4 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST008672 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. Triglyceride levels up to 23,508 African ancestry individuals, 4,649 Asian ancestry individuals, up to 77,047 European ancestry individuals, 6,705 Hispanic individuals NA Affymetrix, Illumina, Perlegen [NR] (imputed) 48 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008702 Genome-wide genotyping array 2019-09-19 30926973 Bentley AR 2019-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30926973 Multi-ancestry genome-wide gene-smoking interaction study of 387,272 individuals identifies new loci associated with serum lipids. HDL cholesterol levels x smoking (current vs non smokers) interaction (1df test) 5,120 African ancestry current smoker individuals, 2,394 Asian ancestry current smoker individuals, 15,129 European ancestry current smoker individuals, 747 Hispanic current smoker individuals, 18,641 African ancestry non smoker individuals, 10,777 Asian ancestry non smoker individuals, 75,138 European ancestry non smoker individuals, 5,873 Hispanic non smoker individuals 1,825 African ancestry current smoker individuals, 16,241 Asian ancestry current smoker individuals, 32,416 European ancestry current smoker individuals, 3,570 Hispanic current smoker individuals, 5,392 African ancestry non smoker individuals, 65,276 Asian ancestry non smoker individuals, 114,795 European ancestry non smoker individuals, 13,952 Hispanic non smoker individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 2 smoking status measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008677 Genome-wide genotyping array 2020-06-06 31178129 Spracklen CN 2019-06-06 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31178129 Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology. Adiponectin levels up to 60,465 European ancestry individuals, up to 2,568 East Asian ancestry individuals, up to 3,271 African American individuals, up to 1,435 Hispanic individuals NA Illumina [265780] 20 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST010050 Exome genotyping array [Exome array] 2021-06-04 33125279 Cordova-Palomera A 2020-10-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33125279 Cardiac Imaging of Aortic Valve Area from 34,287 UK Biobank Participants Reveal Novel Genetic Associations and Shared Genetic Comorbidity with Multiple Disease Phenotypes. Aortic valve area 26,142 British ancestry individuals 8,145 European ancestry individuals Affymetrix [> 4100000] (imputed) 1 cardiovascular measurement http://www.ebi.ac.uk/efo/EFO_0004298 GCST011787 Genome-wide genotyping array 2020-01-27 28346444 Wright DJ 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346444 Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility. Cancer 7,745 European ancestry male cases, 58,562 European ancestry male controls NA Affymetrix [at least 641018] (imputed) 1 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST009503 Genome-wide genotyping array 2020-01-07 28346444 Wright DJ 2017-03-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28346444 Genetic variants associated with mosaic Y chromosome loss highlight cell cycle genes and overlap with cancer susceptibility. Mosaic loss of chromosome Y (Y chromosome dosage) 67,034 European ancestry men 8,715 European ancestry men, 9,793 men Affymetrix [at least 641018] (imputed) 19 mosaic loss of chromosome Y measurement http://www.ebi.ac.uk/efo/EFO_0007783 GCST009375 Genome-wide genotyping array 2019-11-22 31659325 Malhotra R 2019-10-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31659325 HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype. Thoracic aortic calcification levels 8,422 European ancestry individuals NA Affymetrix, Illumina [9000000] (imputed) 8 thoracic aortic calcification measurement http://www.ebi.ac.uk/efo/EFO_0010273 GCST009090 Genome-wide genotyping array 2019-11-22 31659325 Malhotra R 2019-10-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31659325 HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype. Abdominal aortic calcification levels 9,417 European ancestry individuals 1,595 African American individuals, 496 Hispanic or Latin American individuals Affymetrix, Illumina [9000000] (imputed) 8 abdominal aortic calcification measurement http://www.ebi.ac.uk/efo/EFO_0010272 GCST009091 Genome-wide genotyping array 2020-09-24 32605384 Choquet H 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32605384 Meta-analysis of 26,638 Individuals Identifies Two Genetic Loci Associated with Left Ventricular Ejection Fraction. Left ventricular ejection fraction 18,670 European ancestry individuals, 1,207 East Asian ancestry individuals, 1,514 Hispanic/Latino individuals, 764 African American individuals NA Affymetrix [10432573] (imputed) 1 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST90006790 Genome-wide genotyping array 2020-09-24 32605384 Choquet H 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32605384 Meta-analysis of 26,638 Individuals Identifies Two Genetic Loci Associated with Left Ventricular Ejection Fraction. Left ventricular ejection fraction 4,483 European ancestry individuals NA Affymetrix [12703989] (imputed) 1 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST90006791 Genome-wide genotyping array 2020-09-24 32605384 Choquet H 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32605384 Meta-analysis of 26,638 Individuals Identifies Two Genetic Loci Associated with Left Ventricular Ejection Fraction. Left ventricular ejection fraction 23,153 European ancestry individuals, 1,207 East Asian ancestry individuals, 1,514 Hispanic/Latino individuals, 764 African American individuals NA Affymetrix [10432573] (imputed) 2 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST010617 Genome-wide genotyping array 2020-04-29 31801372 Strawbridge RJ 2019-12-05 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31801372 Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UKB. Carotid intima media thickness (mean) 10,708 British ancestry men, 11,471 British ancestry women NA NR [NR] (imputed) 12 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST009921 Genome-wide genotyping array 2020-03-06 31801372 Strawbridge RJ 2019-12-05 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31801372 Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UKB. Carotid intima media thickness (maximum) 22,179 British ancestry individuals NA NR [NR] (imputed) 3 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST009738 Genome-wide genotyping array 2020-03-06 31801372 Strawbridge RJ 2019-12-05 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31801372 Carotid Intima-Media Thickness: Novel Loci, Sex-Specific Effects, and Genetic Correlations With Obesity and Glucometabolic Traits in UKB. Carotid intima media thickness (mean-maximum) 22,179 British ancestry individuals NA NR [NR] (imputed) 12 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST009739 Genome-wide genotyping array 2020-12-06 29930801 Yamada Y 2018-05-29 Biomed Rep www.ncbi.nlm.nih.gov/pubmed/29930801 Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage. Ischemic stroke 450 Japanese ancestry cases, 5,774 Japanese ancestry controls NA Illumina [31245] 10 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST010836 Exome genotyping array 2020-12-06 29930801 Yamada Y 2018-05-29 Biomed Rep www.ncbi.nlm.nih.gov/pubmed/29930801 Identification of nine genes as novel susceptibility loci for early-onset ischemic stroke, intracerebral hemorrhage, or subarachnoid hemorrhage. Intracerebral hemorrhage 261 Japanese ancestry intracerebral hemorrhage cases, 176 Japanese ancestry subarachnoid hemorrhage cases, 5,742 Japanese ancestry controls NA Illumina [30970] 3 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST010837 Exome genotyping array 2020-02-06 31840077 Couto Alves A 2019-09-04 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31840077 GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI. Peak weight velocity 7,215 European ancestry children 5,367 European ancestry children Affymetrix, Illumina [up to 2543888] (imputed) 0 growth rate measurement http://www.ebi.ac.uk/efo/EFO_0010572 GCST009552 Genome-wide genotyping array 2020-02-06 31840077 Couto Alves A 2019-09-04 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31840077 GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI. Age at adiposity peak 6,222 European ancestry children NA Affymetrix, Illumina [up to 2543888] (imputed) 0 longitudinal BMI measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0005937, http://www.ebi.ac.uk/efo/EFO_0008007 GCST009553 Genome-wide genotyping array 2020-02-06 31840077 Couto Alves A 2019-09-04 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31840077 GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI. BMI at adiposity peak 6,219 European ancestry children 16,550 European ancestry children Affymetrix, Illumina [up to 2543888] (imputed) 2 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST009556 Genome-wide genotyping array 2020-02-06 31840077 Couto Alves A 2019-09-04 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31840077 GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI. Age at adiposity rebound 6,051 European ancestry children 12,256 European ancestry children Affymetrix, Illumina [up to 2543888] (imputed) 2 longitudinal BMI measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0005937, http://www.ebi.ac.uk/efo/EFO_0008007 GCST009555 Genome-wide genotyping array 2020-02-06 31840077 Couto Alves A 2019-09-04 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31840077 GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI. BMI at adiposity rebound 6,051 European ancestry children 12,192 European ancestry children Affymetrix, Illumina [up to 2543888] (imputed) 2 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST009554 Genome-wide genotyping array 2020-02-06 31840077 Couto Alves A 2019-09-04 Sci Adv www.ncbi.nlm.nih.gov/pubmed/31840077 GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI. Peak height velocity 6,933 European ancestry children NA Affymetrix, Illumina [up to 2543888] (imputed) 0 growth rate measurement http://www.ebi.ac.uk/efo/EFO_0010572 GCST009551 Genome-wide genotyping array 2019-09-22 31423876 Singh S 2019-08-19 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/31423876 Genome-Wide Meta-Analysis of Blood Pressure Response to β1-Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies). Response to beta blocker use in hypertension (systolic blood pressure) 1,254 European ancestry individuals 1,552 European ancestry individuals, 315 African American individuals Affymetrix, Illumina [6596214] (imputed) 1 systolic blood pressure change measurement, response to beta blocker http://www.ebi.ac.uk/efo/EFO_0006944, http://www.ebi.ac.uk/efo/EFO_0007766 GCST008736 Genome-wide genotyping array 2019-09-22 31423876 Singh S 2019-08-19 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/31423876 Genome-Wide Meta-Analysis of Blood Pressure Response to β1-Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies). Response to beta blocker use in hypertension (diastolic blood pressure) 1,254 European ancestry individuals 1,552 European ancestry individuals, 315 African American individuals Affymetrix, Illumina [6596214] (imputed) 0 diastolic blood pressure change measurement, response to beta blocker http://www.ebi.ac.uk/efo/EFO_0006945, http://www.ebi.ac.uk/efo/EFO_0007766 GCST008735 Genome-wide genotyping array 2020-04-17 31906708 Levey DF 2020-01-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31906708 Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program. Anxiety 175,163 European ancestry individuals, 24,448 African American individuals NA Affymetrix [at least 723305] (imputed) 6 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST009837 Genome-wide genotyping array 2020-04-17 31906708 Levey DF 2020-01-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/31906708 Reproducible Genetic Risk Loci for Anxiety: Results From ∼200,000 Participants in the Million Veteran Program. Anxiety disorders 28,525 European ancestry cases, 5,664 African American cases, 163,731 European ancestry controls, 26,410 African American controls NA Affymetrix [at least 723305] (imputed) 2 anxiety disorder, panic disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0004262 GCST009838 Genome-wide genotyping array 2020-06-23 32390946 Liu L 2020-04-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/32390946 Twelve New Genomic Loci Associated With Bone Mineral Density. Heel bone mineral density (MTAG) 426,824 individuals NA NR [7369691] (imputed) 12 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST010091 Genome-wide genotyping array 2020-06-23 32390946 Liu L 2020-04-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/32390946 Twelve New Genomic Loci Associated With Bone Mineral Density. Total body bone mineral density (MTAG) 66,628 individuals NA Affymetrix, Illumina [7369691] (imputed) 11 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST010092 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Adventurousness 557,923 European ancestry individuals NA Illumina [9339358] (imputed) 167 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST007324 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Automobile speeding propensity 404,291 European ancestry individuals NA Affymetrix [11514463] (imputed) 42 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST007329 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Alcohol consumption (drinks per week) 414,343 European ancestry individuals NA Affymetrix [11514936] (imputed) 85 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST007328 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Smoking status (ever vs never smokers) 518,633 European ancestry individuals NA Affymetrix [11514654] (imputed) 223 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST007327 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Number of sexual partners 370,711 European ancestry individuals NA Affymetrix [11515109] (imputed) 118 risky sexual behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007877 GCST007326 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. General risk tolerance (MTAG) 975,353 European ancestry individuals NA Affymetrix, Illumina [5869552] (imputed) 312 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST007325 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. Risk-taking tendency (4-domain principal component model) 315,894 European ancestry individuals NA Affymetrix [~ 11515000] (imputed) 106 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST007323 Genome-wide genotyping array 2019-03-18 30643258 Karlsson Linner R 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643258 Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. General risk tolerance 939,908 European ancestry individuals 35,445 European ancestry individuals Affymetrix, Illumina [9284738] (imputed) 0 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST007322 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking initiation (ever regular vs never regular) 83,830 Japanese ancestry ever smokers, 81,626 Japanese ancestry never smokers NA Illumina [5961480] (imputed) 1 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST009403 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking initiation (ever regular vs never regular) 67,773 Japanese ancestry ever smoker males, 21,905 Japanese ancestry never smoker males NA Illumina [6108828] (imputed) 2 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST009399 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking initiation (ever regular vs never regular) 16,077 Japanese ancestry ever smoker females, 59,721 Japanese ancestry never smoker females NA Illumina [6108828] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST009402 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking cessation (former vs current smokers) 43,163 Japanese ancestry former smokers, 32,884 Japanese ancestry current smokers NA Illumina [5961480] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST009400 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking cessation (former vs current smokers) 36,787 Japanese ancestry former smoker males, 24,909 Japanese ancestry current smoker males NA Illumina [6108828] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST009401 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking cessation (former vs current smokers) 6,376 Japanese ancestry former smoker females, 7,975 Japanese ancestry current smoker females NA Illumina [6108828] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST009398 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking behaviour (cigarettes smoked per day) 72,655 Japanese ancestry individuals NA Illumina [5961480] (imputed) 6 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST009405 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking behaviour (cigarettes smoked per day) 13,871 Japanese ancestry females NA Illumina [6108828] (imputed) 1 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST009406 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Smoking behaviour (cigarettes smoked per day) 58,784 Japanese ancestry males NA Illumina [6108828] (imputed) 5 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST009407 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Age of smoking initiation 30,418 Japanese ancestry individuals NA Illumina [5961480] (imputed) 0 age at onset, smoking initiation http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0005670 GCST009408 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Age of smoking initiation 7,379 Japanese ancestry females NA Illumina [6108828] (imputed) 1 age at onset, smoking initiation http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0005670 GCST009409 Genome-wide genotyping array 2020-01-09 31089300 Matoba N 2019-03-25 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31089300 GWAS of smoking behaviour in 165,436 Japanese people reveals seven new loci and shared genetic architecture. Age of smoking initiation 23,039 Japanese ancestry males NA Illumina [6108828] (imputed) 0 age at onset, smoking initiation http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0005670 GCST009410 Genome-wide genotyping array 2020-02-18 31754133 Singh S 2019-11-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31754133 Genome Wide Analysis Approach Suggests Chromosome 2 Locus to be Associated with Thiazide and Thiazide Like-Diuretics Blood Pressure Response. Systolic blood pressure response to thiazide and thiazide-like diuretics in hypertension 290 African American individuals, 397 European ancestry individuals NA Illumina [NR] (imputed) 2 response to diuretic, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0006944 GCST009645 Genome-wide genotyping array 2020-02-18 31754133 Singh S 2019-11-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31754133 Genome Wide Analysis Approach Suggests Chromosome 2 Locus to be Associated with Thiazide and Thiazide Like-Diuretics Blood Pressure Response. Diastolic blood pressure response to thiazide and thiazide-like diuretics in hypertension 290 African American individuals, 397 European ancestry individuals NA Illumina [NR] (imputed) 4 response to diuretic, diastolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0006945 GCST009646 Genome-wide genotyping array 2020-02-18 31754133 Singh S 2019-11-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31754133 Genome Wide Analysis Approach Suggests Chromosome 2 Locus to be Associated with Thiazide and Thiazide Like-Diuretics Blood Pressure Response. Systolic blood pressure response to chlorthalidone in hypertension 142 African American individuals, 175 European ancestry individuals NA Illumina [NR] (imputed) 59 response to diuretic, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0006944 GCST009644 Genome-wide genotyping array 2020-02-18 31754133 Singh S 2019-11-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31754133 Genome Wide Analysis Approach Suggests Chromosome 2 Locus to be Associated with Thiazide and Thiazide Like-Diuretics Blood Pressure Response. Diastolic blood pressure response to chlorthalidone in hypertension 142 African American individuals, 175 European ancestry individuals NA Illumina [NR] (imputed) 88 response to diuretic, diastolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0006945 GCST009643 Genome-wide genotyping array 2020-07-22 32266521 Justice CM 2020-04-07 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32266521 A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis. Midline nonsyndromic craniosynostosis 345 European ancestry trios NA Illumina [306233] 2 isolated craniosynostosis http://purl.obolibrary.org/obo/MONDO_0015337 GCST010297 Genome-wide genotyping array 2020-07-22 32266521 Justice CM 2020-04-07 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32266521 A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis. Metopic nonsyndromic craniosynostosis 215 European ancestry trios 194 European ancestry cases, 333 European ancestry controls Illumina [649669] 3 metopic craniosynostosis http://www.ebi.ac.uk/efo/EFO_0008511 GCST010298 Genome-wide genotyping array 2021-01-26 32201043 Smeland OB 2020-02-08 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32201043 Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci. Parkinson's disease 20,184 European ancestry cases, 397,324 European ancestry controls NA Illumina [NR] 55 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST010991 Genome-wide genotyping array 2021-01-26 32201043 Smeland OB 2020-02-08 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32201043 Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci. Parkinson's disease or schizophrenia 34,875 European ancestry schizophrenia cases, 20,184 European ancestry Parkinson's disease cases, 440,781 European ancestry controls NA Illumina [NR] 0 schizophrenia, Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005180 GCST010990 Genome-wide genotyping array 2020-07-21 32205469 Akcimen F 2020-03-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/32205469 Genome-wide association study identifies genetic factors that modify age at onset in Machado-Joseph disease. Machado-Joseph disease (age at onset) 700 cases NA Illumina [6716580] (imputed) 8 Machado-Joseph disease, age at onset http://purl.obolibrary.org/obo/MONDO_0007182, http://www.ebi.ac.uk/efo/EFO_0004847 GCST010248 Genome-wide genotyping array 2022-09-26 32270874 Campa D 2020-04-09 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/32270874 Genome-wide association study identifies an early onset pancreatic cancer risk locus. Pancreatic ductal adenocarcinoma (age of onset)(over 60 vs under 60) 821 European ancestry younger cases, 2,312 European ancestry older cases 2,385 European ancestry younger cases, 7,741 European ancestry older cases NR [630600] 0 age at onset, pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0002618 GCST012978 Genome-wide genotyping array 2022-09-26 32270874 Campa D 2020-04-09 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/32270874 Genome-wide association study identifies an early onset pancreatic cancer risk locus. Early onset pancreatic ductal adenocarcinoma 821 European ancestry cases, 3,227 European ancestry controls 2,031 European ancestry cases, 7,741 European ancestry controls NR [630600] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST012979 Genome-wide genotyping array 2020-03-03 31959993 Craig JE 2020-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31959993 Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Vertical cup-disc ratio (adjusted for vertical disc diameter) 67,040 British ancestry individuals NA Affymetrix [at least 8002429] (imputed) 100 cup-to-disc ratio measurement http://www.ebi.ac.uk/efo/EFO_0006939 GCST009723 Genome-wide genotyping array 2020-03-03 31959993 Craig JE 2020-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31959993 Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Vertical cup-disc ratio (multi-trait analysis) 90,939 European ancestry individuals NA Affymetrix, Illumina [8002429] (imputed) 107 cup-to-disc ratio measurement http://www.ebi.ac.uk/efo/EFO_0006939 GCST009724 Genome-wide genotyping array 2020-03-03 31959993 Craig JE 2020-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31959993 Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Intraocular pressure 133,492 European ancestry individuals NA Affymetrix, Illumina [8002429] (imputed) 95 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST009725 Genome-wide genotyping array 2020-03-03 31959993 Craig JE 2020-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31959993 Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Glaucoma 7,947 British ancestry cases, 119,318 British ancestry controls NA Affymetrix [at least 8002429] (imputed) 39 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST009726 Genome-wide genotyping array 2020-03-03 31959993 Craig JE 2020-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31959993 Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression. Glaucoma (multi-trait analysis) 133,492 European ancestry individuals with intraocular pressure measurements, 90,939 European ancestry individuals with vertical cup-disc ratio measurements, 7,947 British ancestry glaucoma cases, 119,318 British ancestry controls 6,924 European ancestry glaucoma cases, 40,230 European ancestry controls Affymetrix, Illumina [8002429] (imputed) 20 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST009722 Genome-wide genotyping array 2020-07-28 32386560 Ramirez J 2020-04-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32386560 Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval. TPE interval (resting) 71,338 European ancestry individuals NA Affymetrix [~ 9000000] (imputed) 62 TPE interval measurement http://www.ebi.ac.uk/efo/EFO_0004644 GCST010346 Genome-wide genotyping array 2020-07-28 32386560 Ramirez J 2020-04-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32386560 Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval. TPE interval (response to exercise) 51,897 European ancestry individuals NA Affymetrix [~ 9000000] (imputed) 3 TPE interval measurement, response to exercise http://www.ebi.ac.uk/efo/EFO_0004644, http://www.ebi.ac.uk/efo/EFO_0007768 GCST010345 Genome-wide genotyping array 2020-07-28 32386560 Ramirez J 2020-04-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32386560 Common Genetic Variants Modulate the Electrocardiographic Tpeak-to-Tend Interval. TPE interval (recovery after exercise) 51,503 European ancestry individuals NA Affymetrix [~ 9000000] (imputed) 3 TPE interval measurement, response to exercise http://www.ebi.ac.uk/efo/EFO_0004644, http://www.ebi.ac.uk/efo/EFO_0007768 GCST010344 Genome-wide genotyping array 2021-05-19 32407400 Tekola-Ayele F 2020-05-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32407400 Trans-ethnic meta-analysis of genome-wide association studies identifies maternal ITPR1 as a novel locus influencing fetal growth during sensitive periods in pregnancy. fetal weight (maternal genotype effect) 580 European ancestry individuals, 556 African American individuals, 508 Hispanic individuals, 205 East Asian individuals 55 European ancestry individuals, 57 African American individuals, 72 Hispanic individuals Illumina [NR] (imputed) 0 fetal weight, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0011045, http://www.ebi.ac.uk/efo/EFO_0005939 GCST011698 Genome-wide genotyping array 2020-01-15 31097437 Plotnikov D 2019-05-16 Br J Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31097437 Association between birth weight and refractive error in adulthood: a Mendelian randomisation study. Birth weight 188,039 European ancestry individuals NA Affymetrix [up to 10400000] (imputed) 73 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST009437 Genome-wide genotyping array 2020-01-15 31097437 Plotnikov D 2019-05-16 Br J Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31097437 Association between birth weight and refractive error in adulthood: a Mendelian randomisation study. Refractive error 139,884 European ancestry individuals NA Affymetrix [up to 10400000] (imputed) 0 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST009436 Genome-wide genotyping array 2020-01-22 24777453 Auer PL 2014-04-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24777453 Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Platelet count 24,814 European ancestry individuals 6,526 European ancestry individuals Illumina [183585] 4 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST009465 Exome genotyping array [Exome array] 2020-01-22 24777453 Auer PL 2014-04-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24777453 Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Hematocrit 24,814 European ancestry individuals 6,526 European ancestry individuals Illumina [183585] 2 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST009466 Exome genotyping array [Exome array] 2020-01-22 24777453 Auer PL 2014-04-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24777453 Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Hemoglobin levels 24,814 European ancestry individuals 6,526 European ancestry individuals Illumina [183585] 4 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST009467 Exome genotyping array [Exome array] 2020-01-22 24777453 Auer PL 2014-04-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24777453 Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. White blood cell count 24,814 European ancestry individuals 6,526 European ancestry individuals Illumina [183585] 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST009468 Exome genotyping array [Exome array] 2019-05-30 30995994 Truong DT 2019-04-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30995994 Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Latent naming speed 441 African American children NA Illumina [1265623] 0 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007862 Genome-wide genotyping array 2019-05-30 30995994 Truong DT 2019-04-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30995994 Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Latent naming speed 883 Hispanic American children NA Illumina [1265623] 0 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007861 Genome-wide genotyping array 2019-05-30 30995994 Truong DT 2019-04-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30995994 Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Rapid automised naming and rapid alternating stimulus test performance 883 Hispanic American children, 441 African American children NA Illumina [1265623] 4 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007859 Genome-wide genotyping array 2019-05-30 30995994 Truong DT 2019-04-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30995994 Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Latent naming speed 883 Hispanic American children, 441 African American children NA Illumina [1265623] 7 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007860 Genome-wide genotyping array 2019-05-30 30995994 Truong DT 2019-04-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30995994 Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Rapid automised naming of objects 883 Hispanic American children, 441 African American children NA Illumina [1265623] 0 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007865 Genome-wide genotyping array 2019-05-30 30995994 Truong DT 2019-04-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30995994 Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Rapid automised naming of letters 883 Hispanic American children, 441 African American children NA Illumina [1265623] 3 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007864 Genome-wide genotyping array 2019-05-30 30995994 Truong DT 2019-04-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30995994 Multivariate genome-wide association study of rapid automatised naming and rapid alternating stimulus in Hispanic American and African-American youth. Rapid alternating stimulus test for letters/numbers 883 Hispanic American children, 441 African American children NA Illumina [1265623] 3 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007863 Genome-wide genotyping array 2022-09-21 31797139 Elgaeva EE 2019-12-03 Eur Spine J www.ncbi.nlm.nih.gov/pubmed/31797139 ISSLS Prize in Clinical Science 2020. Examining causal effects of body mass index on back pain: a Mendelian randomization study. Back pain 120,842 European ancestry cases, 333,018 European ancestry controls NA Affymetrix [NR] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST012958 Genome-wide genotyping array 2019-09-16 31482010 Liu C 2019-08-29 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/31482010 Genome-wide association study for proliferative diabetic retinopathy in Africans. Proliferative diabetic retinopathy 64 African ancestry cases, 227 African ancestry controls 19 African American cases, 50 African American controls Affymetrix, Illumina [18433741] (imputed) 4 proliferative diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0009322 GCST008668 Genome-wide genotyping array 2020-01-07 31755389 Li J 2019-11-21 Curr Alzheimer Res www.ncbi.nlm.nih.gov/pubmed/31755389 Genome-wide Network-assisted Association and Enrichment Study of Amyloid Imaging Phenotype in Alzheimer's Disease. Cerebral cortex AV-45 amyloid PET measurement 155 cognitively normal individuals, 72 significant memory concern individuals, 278 with early mild cognitive impairment individuals, 144 late mild cognitive impairment individuals, 125 Alzheimer's disease cases. NA Illumina [563980] 1 cerebral amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0007707 GCST009376 Genome-wide genotyping array 2020-01-15 31095298 Huang M 2019-05-16 Bioinformatics www.ncbi.nlm.nih.gov/pubmed/31095298 Incorporating spatial-anatomical similarity into the VGWAS framework for AD biomarker detection. Voxel-wise structural brain imaging measurements in Alzheimer’s disease 708 European ancestry individuals NA Illumina [501584] 15 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST009438 Genome-wide genotyping array 2021-03-18 31687947 Kobakhidze N 2019-09-01 Georgian Med News www.ncbi.nlm.nih.gov/pubmed/31687947 NEW GENETIC MARKERS ASSOCIATED WITH SUSCEPTIBILITY TO EXFOLIATION SYNDROME AMONG GEORGIAN POPULATION. Exfoliation syndrome 132 Georgian ancestry cases, 199 Georgian ancestry controls NA Illumina [at least 680000] 0 exfoliation syndrome http://www.ebi.ac.uk/efo/EFO_0004235 GCST011297 Genome-wide genotyping array 2019-02-01 30573740 Yap CX 2018-12-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30573740 Dissection of genetic variation and evidence for pleiotropy in male pattern baldness. Male-pattern baldness 205,327 European ancestry males NA NR [19129689] (imputed) 622 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST007020 Genome-wide genotyping array 2019-03-11 30573655 Acosta-Herrera M 2018-12-20 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/30573655 Genome-wide meta-analysis reveals shared new loci in systemic seropositive rheumatic diseases. Systemic seropositive rheumatic diseases (Systemic sclerosis or systemic lupus erythematosus or rheumatoid arthritis or idiopathic inflammatory myopathies) up to 4,595 European ancestry rheumatoid arthritis cases, up to 3,154 European ancestry systemic lupus erythematosus cases, up to 2,281 European ancestry systemic sclerosis cases, up to 1,674 European ancestry idiopathic inflammatory myopathy cases, 19,704 European ancestry controls NA Illumina [6450125] (imputed) 26 systemic scleroderma, rheumatoid arthritis, myositis, systemic lupus erythematosus http://www.ebi.ac.uk/efo/EFO_0000717, http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0000783, http://purl.obolibrary.org/obo/MONDO_0007915 GCST007278 Genome-wide genotyping array 2019-11-26 31689377 Wootton RE 2019-11-06 Psychol Med www.ncbi.nlm.nih.gov/pubmed/31689377 Evidence for causal effects of lifetime smoking on risk for depression and schizophrenia: a Mendelian randomisation study. Lifetime smoking index 462,690 European ancestry individuals NA Affymetrix [up to 90000000] (imputed) 126 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST009096 Genome-wide genotyping array 2019-10-16 31562340 Akiyama M 2019-09-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31562340 Characterizing rare and low-frequency height-associated variants in the Japanese population. Height 159,095 Japanese ancestry individuals 32,692 Japanese ancestry individuals Illumina [27896057] (imputed) 608 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST008839 Genome-wide genotyping array 2020-09-07 32393786 Meddens SFW 2020-05-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32393786 Genomic analysis of diet composition finds novel loci and associations with health and lifestyle. Relative fat intake 175,253 European ancestry individuals 93,179 European ancestry individuals Affymetrix [NR] 4 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST010499 Genome-wide genotyping array 2020-09-07 32393786 Meddens SFW 2020-05-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32393786 Genomic analysis of diet composition finds novel loci and associations with health and lifestyle. Relative protein intake 175,253 European ancestry individuals 93,179 European ancestry individuals Affymetrix [NR] 5 protein intake measurement http://www.ebi.ac.uk/efo/EFO_0010810 GCST010498 Genome-wide genotyping array 2020-09-07 32393786 Meddens SFW 2020-05-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32393786 Genomic analysis of diet composition finds novel loci and associations with health and lifestyle. Relative carbohydrate intake 175,253 European ancestry individuals 93,179 European ancestry individuals Affymetrix [NR] 7 carbohydrate intake measurement http://www.ebi.ac.uk/efo/EFO_0010811 GCST010497 Genome-wide genotyping array 2020-09-07 32393786 Meddens SFW 2020-05-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32393786 Genomic analysis of diet composition finds novel loci and associations with health and lifestyle. Relative sugar intake 175,253 European ancestry individuals 59,454 European ancestry individuals Affymetrix [NR] 5 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST010496 Genome-wide genotyping array 2020-07-03 31801373 Choi Y 2019-12-05 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31801373 Causal Associations Between Serum Bilirubin Levels and Decreased Stroke Risk: A Two-Sample Mendelian Randomization Study. Bilirubin levels 25,406 Korean ancestry individuals NA NR [NR] (imputed) 7 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST010117 Genome-wide genotyping array 2021-03-28 32759990 Carlson JC 2020-08-05 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32759990 Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels. HDL cholesterol levels 2,849 Samoan (founder/genetic isolate) individuals 1,798 Samoan and American Samoan (founder/genetic isolate) individuals Affymetrix [659492] 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST011418 Genome-wide genotyping array 2021-03-28 32759990 Carlson JC 2020-08-05 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32759990 Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels. LDL cholesterol levels 2,849 Samoan (founder/genetic isolate) individuals 1,798 Samoan and American Samoan (founder/genetic isolate) individuals Affymetrix [659492] 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST011417 Genome-wide genotyping array 2021-03-28 32759990 Carlson JC 2020-08-05 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32759990 Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels. Triglyceride levels 2,849 Samoan (founder/genetic isolate) individuals 1,798 Samoan and American Samoan (founder/genetic isolate) individuals Affymetrix [659492] 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011416 Genome-wide genotyping array 2021-03-28 32759990 Carlson JC 2020-08-05 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32759990 Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels. Total cholesterol levels 2,849 Samoan (founder/genetic isolate) individuals 1,798 Samoan and American Samoan (founder/genetic isolate) individuals Affymetrix [659492] 2 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST011419 Genome-wide genotyping array 2021-06-14 32409696 Hong M 2020-05-15 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32409696 Potential causal association of a prolonged PR interval and clinical recurrence of atrial fibrillation after catheter ablation: a Mendelian randomization analysis. PR interval in atrial fibrillation treated with catheter ablation 586 cases, 1,136 controls NA NR [403402] 0 cardiac ablation, PR interval http://www.ebi.ac.uk/efo/EFO_0600009, http://www.ebi.ac.uk/efo/EFO_0004462 GCST011856 Genome-wide genotyping array 2020-07-12 29234017 Carayol J 2017-12-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29234017 Protein quantitative trait locus study in obesity during weight-loss identifies a leptin regulator. Protein level change in low calorie diet obesity intervention 494 European ancestry individuals NA Illumina [4020654] (imputed) 8 response to low calorie diet, protein measurement http://www.ebi.ac.uk/efo/EFO_0010731, http://www.ebi.ac.uk/efo/EFO_0004747 GCST010197 Genome-wide genotyping array 2020-07-12 29234017 Carayol J 2017-12-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29234017 Protein quantitative trait locus study in obesity during weight-loss identifies a leptin regulator. Protein levels in obesity 494 European ancestry individuals NA Illumina [4020654] (imputed) 58 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST010196 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Hematological and biochemical traits up to 6,843 Korean ancestry individuals NA Affymetrix [305158] 9 hemoglobin measurement, diastolic blood pressure, systolic blood pressure, hemoglobin A1 measurement, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0007629, http://www.ebi.ac.uk/efo/EFO_0004465 GCST010062 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Lung function up to 4,291 Korean ancestry individuals NA Affymetrix [305158] 1 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST010061 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Cholesterol 6,840 Korean ancestry individuals NA Affymetrix [305158] 14 total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004612 GCST010060 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Physiological traits up to 6,835 Korean ancestry individuals NA Affymetrix [305158] 5 waist circumference, body weight, body mass index, body height http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004339 GCST010063 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Physiological traits up to 6,835 Korean ancestry individuals NA Affymetrix [305158] 10 waist circumference, longitudinal BMI measurement, body weight, body height http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0005937, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004339 GCST010059 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Hematological and biochemical traits up to 6,843 Korean ancestry individuals NA Affymetrix [305158] 2 hemoglobin measurement, diastolic blood pressure change measurement, hemoglobin A1 measurement, systolic blood pressure change measurement, fasting blood glucose change measurement http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0006945, http://www.ebi.ac.uk/efo/EFO_0007629, http://www.ebi.ac.uk/efo/EFO_0006944, http://www.ebi.ac.uk/efo/EFO_0010120 GCST010058 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Lung function up to 4,291 Korean ancestry individuals NA Affymetrix [305158] 9 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST010057 Genome-wide genotyping array 2020-06-11 31902109 Li D 2020-01-04 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/31902109 Progressive effects of single-nucleotide polymorphisms on 16 phenotypic traits based on longitudinal data. Cholesterol 6,840 Korean ancestry individuals NA Affymetrix [305158] 2 HDL cholesterol change measurement, triglyceride change measurement, LDL cholesterol change measurement, total cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805, http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0007804, http://www.ebi.ac.uk/efo/EFO_0007806 GCST010056 Genome-wide genotyping array 2020-04-17 31960908 Nag A 2020-01-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31960908 Genome-wide scan identifies novel genetic loci regulating salivary metabolite levels. Salivary metabolite levels 1,419 European ancestry individuals 1,000 European ancestry individuals Illumina [9600000] (imputed) 4 salivary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0010637 GCST009885 Genome-wide genotyping array 2020-07-22 32308125 Wolking S 2020-04-20 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/32308125 Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Response to antiepileptic drugs in genetic generalized epilepsy 608 European ancestry responders, 278 European ancestry non-responders NA Affymetrix, Illumina [at least 3287443] (imputed) 4 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST010296 Genome-wide genotyping array 2020-07-22 32308125 Wolking S 2020-04-20 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/32308125 Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Response to valproic acid in genetic generalized epilepsy 410 European ancestry responders, 155 European ancestry non-responders NA Affymetrix, Illumina [at least 3287443] (imputed) 3 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST010295 Genome-wide genotyping array 2020-07-22 32308125 Wolking S 2020-04-20 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/32308125 Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Response to lamotrigine in genetic generalized epilepsy 137 European ancestry responders, 250 European ancestry non-responders NA Affymetrix, Illumina [at least 3287443] (imputed) 4 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST010294 Genome-wide genotyping array 2020-07-22 32308125 Wolking S 2020-04-20 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/32308125 Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Response to levetiracetam in genetic generalized epilepsy 82 European ancestry responders, 127 European ancestry non-responders NA Affymetrix, Illumina [at least 3287443] (imputed) 9 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST010293 Genome-wide genotyping array 2020-07-22 32308125 Wolking S 2020-04-20 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/32308125 Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study. Response to lamotrigine and valproic acid in genetic generalized epilepsy 31 European ancestry responders, 73 European ancestry non-responders NA Affymetrix, Illumina [at least 3287443] (imputed) 7 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST010292 Genome-wide genotyping array 2020-04-15 32063569 Alemany-Navarro M 2020-01-29 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/32063569 Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach. Obsessive compulsive disorder severity 376 Spanish ancestry individuals NA Illumina [338357] 5 obsessive-compulsive disorder, obsessive-compulsive symptom measurement http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0007802 GCST009818 Genome-wide genotyping array 2020-04-15 32063569 Alemany-Navarro M 2020-01-29 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/32063569 Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach. Compulsion score in obsessive compulsive disorder 376 Spanish ancestry individuals NA Illumina [338357] 4 obsessive-compulsive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007802 GCST009819 Genome-wide genotyping array 2020-04-15 32063569 Alemany-Navarro M 2020-01-29 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/32063569 Exploring genetic variants in obsessive compulsive disorder severity: A GWAS approach. Obsession score in obsessive compulsive disorder 376 Spanish ancestry individuals NA Illumina [338357] 1 obsessive-compulsive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007802 GCST009820 Genome-wide genotyping array 2021-02-16 32077919 Antikainen AAV 2020-02-20 Cardiovasc Res www.ncbi.nlm.nih.gov/pubmed/32077919 Genome-wide association study on coronary artery disease in type 1 diabetes suggests beta-defensin 127 as a risk locus. Coronary artery disease in type 1 diabetes 941 European ancestry cases, 3,928 European ancestry controls 434 cases, 3,123 controls Illumina [8744746] (imputed) 9 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST011116 Genome-wide genotyping array 2022-09-21 32061372 O'Connell KS 2019-11-29 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32061372 Identification of Genetic Loci Shared Between Attention-Deficit/Hyperactivity Disorder, Intelligence, and Educational Attainment. Attention deficit hyperactivity disorder, intelligence or educational attainment (pleiotropy) 19,099 European ancestry attention deficit hyperactivity disorder cases, 842,499 European ancestry individuals with educational attainment measurements, 269,867 European ancestry individuals with general intelligence measurements, 34,194 European ancestry controls NA Illumina [NR] 0 attention deficit hyperactivity disorder, intelligence, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0004784 GCST012957 Genome-wide genotyping array 2020-07-21 32080354 Rasmussen ER 2020-02-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/32080354 Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment. Angioedema in response to angiotensin-converting enzyme inhibitor and/or angiotensin receptor blocker 172 European ancestry cases, 1 case, 4,890 European ancestry controls NA Illumina [7585599] (imputed) 19 response to angiotensin-converting enzyme inhibitor, response to angiotensin receptor blocker, angioedema http://www.ebi.ac.uk/efo/EFO_0005325, http://www.ebi.ac.uk/efo/EFO_0010735, http://www.ebi.ac.uk/efo/EFO_0005532 GCST010247 Genome-wide genotyping array 2020-07-21 32080354 Rasmussen ER 2020-02-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/32080354 Genome-wide association study of angioedema induced by angiotensin-converting enzyme inhibitor and angiotensin receptor blocker treatment. Angioedema in response to angiotensin-converting enzyme inhibitor and/or angiotensin receptor blocker 172 European ancestry cases, 1 case, 1,345 European ancestry treated controls 347 European ancestry cases, 66 African ancestry cases, 440 European ancestry treated controls, 157 African ancestry treated controls Illumina [7585599] (imputed) 0 response to angiotensin-converting enzyme inhibitor, response to angiotensin receptor blocker, angioedema http://www.ebi.ac.uk/efo/EFO_0005325, http://www.ebi.ac.uk/efo/EFO_0010735, http://www.ebi.ac.uk/efo/EFO_0005532 GCST010246 Genome-wide genotyping array 2020-07-08 32047264 Cordova-Palomera A 2020-02-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32047264 Genetic control of variability in subcortical and intracranial volumes. Brain imaging measurements (variance) 25,575 European ancestry individuals NA NR [~ 5000000] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST010149 Genome-wide genotyping array 2020-07-08 32047264 Cordova-Palomera A 2020-02-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32047264 Genetic control of variability in subcortical and intracranial volumes. Brain imaging measurements (mean) 25,575 European ancestry individuals NA NR [~ 5000000] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST010150 Genome-wide genotyping array 2019-01-28 30598549 Morris JA 2018-12-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30598549 An atlas of genetic influences on osteoporosis in humans and mice. Heel bone mineral density 426,824 British ancestry individuals NA NR [13737936] (imputed) 1103 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST006979 Genome-wide genotyping array 2019-01-28 30598549 Morris JA 2018-12-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30598549 An atlas of genetic influences on osteoporosis in humans and mice. Fractures 53,184 British ancestry cases, 373,611 British ancestry controls 367,900 European ancestry cases, 363,919 European ancestry controls NR [13977204] (imputed) 14 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST006980 Genome-wide genotyping array 2020-05-28 32072174 Okamoto D 2020-02-19 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/32072174 Genetic Analysis of Ulcerative Colitis in Japanese Individuals Using Population-specific SNP Array. Ulcerative colitis 601 Japanese ancestry cases, 1,962 Japanese ancestry controls 1,075 Japanese ancestry cases, 419 Japanese ancestry controls NR [4760823] (imputed) 3 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST010001 Genome-wide genotyping array 2020-03-10 32060260 Campos AI 2020-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32060260 Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Snoring 151,836 British ancestry cases, 255,230 British ancestry controls NA NR [11010159] (imputed) 35 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST009761 Genome-wide genotyping array 2020-03-10 32060260 Campos AI 2020-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32060260 Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Snoring 90,806 British ancestry male cases, 99,165 British ancestry male controls NA NR [11010159] (imputed) 11 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST009762 Genome-wide genotyping array 2020-03-10 32060260 Campos AI 2020-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32060260 Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Snoring 61,792 British ancestry female cases, 156,554 British ancestry female controls NA NR [11010159] (imputed) 28 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST009763 Genome-wide genotyping array 2020-03-10 32060260 Campos AI 2020-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32060260 Insights into the aetiology of snoring from observational and genetic investigations in the UK Biobank. Snoring 152,302 British ancestry cases, 256,015 British ancestry controls NA NR [11010159] (imputed) 41 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST009760 Genome-wide genotyping array 2020-04-17 30371334 Tuteja S 2018-10-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30371334 Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin. LDL cholesterol change in response to niacin in statin-treated individuals up to 1,034 European ancestry cases, up to 1,020 European ancestry controls NA Illumina [177496] 0 response to statin, LDL cholesterol change measurement, response to vitamin B3 http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0007804, http://www.ebi.ac.uk/efo/EFO_0010648 GCST009883 Targeted genotyping array [Metabochip] 2020-04-17 30371334 Tuteja S 2018-10-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30371334 Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin. Triglycerides levels in response to niacin in statin-treated individuals up to 1,034 European ancestry cases, up to 1,020 European ancestry controls NA Illumina [177496] 0 response to statin, triglyceride change measurement, response to vitamin B3 http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0007681, http://www.ebi.ac.uk/efo/EFO_0010648 GCST009884 Targeted genotyping array [Metabochip] 2020-04-17 30371334 Tuteja S 2018-10-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30371334 Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin. Total cholesterol change in response to niacin in statin-treated individuals up to 1,034 European ancestry cases, up to 1,020 European ancestry controls NA Illumina [177496] 0 response to statin, total cholesterol change measurement, response to vitamin B3 http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0007806, http://www.ebi.ac.uk/efo/EFO_0010648 GCST009882 Targeted genotyping array [Metabochip] 2020-04-17 30371334 Tuteja S 2018-10-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30371334 Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin. Lipoprotein (a) levels in response to niacin in statin-treated individuals up to 1,034 European ancestry cases, up to 1,020 European ancestry controls NA Illumina [177496] 1 response to statin, lipoprotein A measurement, response to vitamin B3 http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0006925, http://www.ebi.ac.uk/efo/EFO_0010648 GCST009881 Targeted genotyping array [Metabochip] 2020-04-17 30371334 Tuteja S 2018-10-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30371334 Genetic Variants Associated With Plasma Lipids Are Associated With the Lipid Response to Niacin. HDL cholesterol change in response to niacin in statin-treated individuals up to 1,034 European ancestry cases, up to 1,020 European ancestry controls NA Illumina [177496] 1 HDL cholesterol change measurement, response to statin, response to vitamin B3 http://www.ebi.ac.uk/efo/EFO_0007805, http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0010648 GCST009880 Targeted genotyping array [Metabochip] 2020-07-21 32203549 Richardson TG 2020-03-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32203549 Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis. LDL cholesterol levels 440,546 European ancestry individuals NA Affymetrix [NR] (imputed) 229 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST010245 Genome-wide genotyping array 2020-07-21 32203549 Richardson TG 2020-03-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32203549 Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis. Triglyceride levels 441,016 European ancestry individuals NA Affymetrix [NR] (imputed) 440 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST010244 Genome-wide genotyping array 2020-07-21 32203549 Richardson TG 2020-03-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32203549 Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis. Apolipoprotein B levels 439,214 European ancestry individuals NA Affymetrix [NR] (imputed) 255 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST010243 Genome-wide genotyping array 2020-07-21 32203549 Richardson TG 2020-03-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32203549 Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis. HDL cholesterol levels 403,943 European ancestry individuals NA Affymetrix [NR] (imputed) 534 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST010242 Genome-wide genotyping array 2020-07-21 32203549 Richardson TG 2020-03-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32203549 Evaluating the relationship between circulating lipoprotein lipids and apolipoproteins with risk of coronary heart disease: A multivariable Mendelian randomisation analysis. Apolipoprotein A1 levels 393,193 European ancestry individuals NA Affymetrix [NR] (imputed) 440 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST010241 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Cardioembolic stroke (CCSp classification) 3,608 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 3 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST010166 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Cardioembolic stroke (TOAST classification) 3,333 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 2 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST010165 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Cardioembolic stroke (CCS and TOAST classification) 2,219 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 3 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST010164 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Cardioembolic stroke (CCS or TOAST classification) 4,502 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 2 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST010163 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Large artery stroke (CCSc classification) 1,565 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 0 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST010162 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Large artery stroke (CCSp classification)j 2,449 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 2 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST010161 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Large artery stroke (TOAST classification) 2,318 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 2 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST010160 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Large artery stroke (CCS and TOAST classification) 1,328 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 2 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST010159 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Large artery stroke (CCS or TOAST classification) 3,495 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 2 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST010158 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Small vessel stroke (CCSc classification) 2,262 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST010157 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Small vessel stroke (CCSp classification) 2,419 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 2 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST010156 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Small vessel stroke (TOAST classification) 2,631 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST010155 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Small vessel stroke (CCS and TOAST classification) 1,548 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 1 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST010154 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Small vessel stroke (CCS or TOAST classification) 3,480 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 1 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST010153 Genome-wide genotyping array 2020-07-09 32047268 von Berg J 2020-02-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32047268 Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke. Cardioembolic stroke (CCSc classification) 3,000 European and African ancestry cases, 28,026 European and unknown ancestry controls NA Illumina [~ 10156805] (imputed) 4 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST010167 Genome-wide genotyping array 2020-04-17 32131869 Arbeeva L 2020-03-04 J Foot Ankle Res www.ncbi.nlm.nih.gov/pubmed/32131869 Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians. Hallux valgus 609 European ancestry male cases, 1,666 European ancestry male controls NA Affymetrix, Illumina [up to 7729175] (imputed) 17 Hallux valgus http://purl.obolibrary.org/obo/HP_0001822 GCST009846 Genome-wide genotyping array 2020-04-17 32131869 Arbeeva L 2020-03-04 J Foot Ankle Res www.ncbi.nlm.nih.gov/pubmed/32131869 Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians. Hallux valgus 1,705 European ancestry female cases, 1,945 European ancestry female controls NA Affymetrix, Illumina [up to 7729175] (imputed) 14 Hallux valgus http://purl.obolibrary.org/obo/HP_0001822 GCST009849 Genome-wide genotyping array 2020-04-17 32131869 Arbeeva L 2020-03-04 J Foot Ankle Res www.ncbi.nlm.nih.gov/pubmed/32131869 Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians. Hallux valgus 2,314 European ancestry cases, 3,611 European ancestry controls NA Affymetrix, Illumina [up to 7729175] (imputed) 14 Hallux valgus http://purl.obolibrary.org/obo/HP_0001822 GCST009847 Genome-wide genotyping array 2022-09-26 32152362 Ran S 2020-03-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32152362 Association of 3p27.1 Variants with Whole Body Lean Mass Identified by a Genome-wide Association Study. Lean body mass 6,004 European ancestry individuals 2,207 European ancestry individuals Affymetrix [6879267] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST012977 Genome-wide genotyping array 2020-07-09 32149159 Chen YM 2020-02-14 J Immunol Res www.ncbi.nlm.nih.gov/pubmed/32149159 Genetic Association and Expression Correlation between Colony-Stimulating Factor 1 Gene Encoding M-CSF and Adult-Onset Still's Disease. Adult onset Still's disease 70 Han Chinese ancestry cases, 688 Han Chinese ancestry controls 36 Han Chinese ancestry cases, 200 Han Chinese ancestry controls Affymetrix [645983] 1 adult-onset Still's disease http://www.ebi.ac.uk/efo/EFO_0007135 GCST010175 Genome-wide genotyping array 2020-01-28 31676860 Zhao B 2019-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31676860 Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits. Brain region volumes 21,821 European ancestry individuals NA NR [8938185] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST009519 Genome-wide genotyping array 2020-01-28 31676860 Zhao B 2019-11-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31676860 Genome-wide association analysis of 19,629 individuals identifies variants influencing regional brain volumes and refines their genetic co-architecture with cognitive and mental health traits. Brain region volumes 19,629 British ancestry individuals NA NR [9227495] (imputed) 1080 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST009518 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Meat-related diet 154,123 European ancestry men, 181,453 European ancestry women NA Affymetrix [25921788] (imputed) 40 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010143 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Pork consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 52 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010140 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Poultry consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010139 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Raw vegetable consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 17 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010138 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Cooked vegetable consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 9 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010137 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Fruit consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 53 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010136 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Oily fish consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 52 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010135 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Non-oily fish consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 7 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010134 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Lamb consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 18 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010133 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Processed meat consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 15 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010132 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Fish- and plant-related diet 154,123 European ancestry men, 181,453 European ancestry women NA Affymetrix [25921788] (imputed) 94 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010142 Genome-wide genotyping array 2020-07-08 32066663 Niarchou M 2020-02-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32066663 Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits. Beef consumption 335,576 European ancestry individuals NA Affymetrix [25921788] (imputed) 7 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010141 Genome-wide genotyping array 2022-09-26 32152295 Lutz MW 2020-03-09 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32152295 Shared genetic etiology underlying Alzheimer's disease and major depressive disorder. Late-onset Alzheimer's disease or major depressive disorder (pleiotropy) 21,982 European ancestry Alzheimer's disease cases, 59,851 major depressive disorder cases, 41,944 European ancestry controls, 113,154 controls NA NR [9154389] (imputed) 0 unipolar depression, late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_1001870 GCST012976 Genome-wide genotyping array 2020-05-29 32152699 Nudel R 2020-03-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32152699 A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness. Gastrointestinal infection 7,197 Danish ancestry cases, 37,062 Danish ancestry controls NA Illumina [11600722] (imputed) 20 digestive system infectious disorder http://purl.obolibrary.org/obo/MONDO_0043424 GCST010008 Genome-wide genotyping array 2020-07-08 32062564 Guo Y 2020-02-06 Neuroimage Clin www.ncbi.nlm.nih.gov/pubmed/32062564 Genome-wide association study of white matter hyperintensity volume in elderly persons without dementia. White matter hyperintensity volume 350 European ancestry elderly individuals NA Illumina [695203] (imputed) 3 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST010147 Genome-wide genotyping array 2020-07-21 32238385 Nakayama A 2020-04-01 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32238385 Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients. Gout 3,053 Japanese ancestry male cases, 4,554 Japanese ancestry male controls NA Illumina [7206774] (imputed) 17 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST010277 Genome-wide genotyping array 2020-07-21 32238385 Nakayama A 2020-04-01 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32238385 Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients. Renal underexcretion gout 654 Japanese ancestry male cases, 4,554 Japanese ancestry male controls NA Illumina [7206774] (imputed) 14 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST010276 Genome-wide genotyping array 2020-07-21 32238385 Nakayama A 2020-04-01 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32238385 Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients. Renal overload gout 486 Japanese ancestry male cases, 4,554 Japanese ancestry male controls NA Illumina [7206774] (imputed) 5 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST010275 Genome-wide genotyping array 2020-07-21 32238385 Nakayama A 2020-04-01 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32238385 Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients. Gout (combined type) 905 Japanese ancestry male cases, 4,554 Japanese ancestry male controls NA Illumina [7206774] (imputed) 9 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST010274 Genome-wide genotyping array 2020-07-21 32238385 Nakayama A 2020-04-01 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32238385 Subtype-specific gout susceptibility loci and enrichment of selection pressure on ABCG2 and ALDH2 identified by subtype genome-wide meta-analyses of clinically defined gout patients. Gout (normal type) 92 Japanese ancestry male cases, 4,554 Japanese ancestry male controls NA Illumina [7206774] (imputed) 11 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST010273 Genome-wide genotyping array 2020-07-21 32235003 Arbeev KG 2020-04-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/32235003 Genetics of physiological dysregulation: findings from the long life family study using joint models. Physiological dysregulation (Mahalanobis distance) 4,608 European ancestry individuals NA Illumina [1464300] 3 hematological measurement, pulmonary function measurement, blood pressure, grip strength measurement, lipoprotein measurement, vital capacity http://www.ebi.ac.uk/efo/EFO_0004503, http://www.ebi.ac.uk/efo/EFO_0003892, http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0006941, http://www.ebi.ac.uk/efo/EFO_0004732, http://www.ebi.ac.uk/efo/EFO_0004312 GCST010279 Genome-wide genotyping array 2020-07-21 32235003 Arbeev KG 2020-04-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/32235003 Genetics of physiological dysregulation: findings from the long life family study using joint models. Hand grip strength (Mahalanobis distance) 4,608 European ancestry individuals NA Illumina [1464300] 8 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST010278 Genome-wide genotyping array 2020-10-27 32227112 Lee MA 2020-03-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/32227112 Common variation at 16p11.2 is associated with glycosuria in pregnancy: Findings from a genome-wide association study in European women. Glycosuria in pregnancy (maternal genotype effect) 1,249 European ancestry cases, 5,140 European ancestry controls NA Illumina [9323831] (imputed) 2 gestational blood glucose measurement, parental genotype effect measurement, Glycosuria http://www.ebi.ac.uk/efo/EFO_0009698, http://www.ebi.ac.uk/efo/EFO_0005939, http://purl.obolibrary.org/obo/HP_0003076 GCST010720 Genome-wide genotyping array 2020-10-27 32227112 Lee MA 2020-03-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/32227112 Common variation at 16p11.2 is associated with glycosuria in pregnancy: Findings from a genome-wide association study in European women. Glycosuria in pregnancy (offspring genotype effect) 747 European ancestry cases, 2,991 European ancestry controls NA Illumina [9873828] (imputed) 5 gestational blood glucose measurement, fetal genotype effect measurement, Glycosuria http://www.ebi.ac.uk/efo/EFO_0009698, http://www.ebi.ac.uk/efo/EFO_0007959, http://purl.obolibrary.org/obo/HP_0003076 GCST010719 Genome-wide genotyping array 2020-10-27 32227112 Lee MA 2020-03-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/32227112 Common variation at 16p11.2 is associated with glycosuria in pregnancy: Findings from a genome-wide association study in European women. Glycosuria in pregnancy (maternal and offspring genotype effect) 1,996 European ancestry cases, 8,131 European ancestry controls NA Illumina [up to 9873828] (imputed) 1 gestational blood glucose measurement, fetal genotype effect measurement, parental genotype effect measurement, Glycosuria http://www.ebi.ac.uk/efo/EFO_0009698, http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0005939, http://purl.obolibrary.org/obo/HP_0003076 GCST010718 Genome-wide genotyping array 2020-06-16 32246137 Meng W 2020-04-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/32246137 A genome-wide association study finds genetic variants associated with neck or shoulder pain in UK Biobank. Neck pain or shoulder pain 53,994 European ancestry cases, 149,312 European ancestry controls 5,035 cases, 18,545 controls NR [9304965] (imputed) 4 Shoulder pain, Neck pain http://purl.obolibrary.org/obo/HP_0030834, http://purl.obolibrary.org/obo/HP_0030833 GCST010080 Genome-wide genotyping array 2019-12-19 31701892 Nalls MA 2019-12-01 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/31701892 Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. Parkinson's disease or first degree relation to individual with Parkinson's disease 15,056 European ancestry cases, 18,618 European ancestry proxy cases, 449,056 European ancestry controls 22,632 European ancestry cases, 968,735 European ancestry controls NR [7784415] (imputed) 107 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST009325 Genome-wide genotyping array 2019-12-19 31701892 Nalls MA 2019-12-01 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/31701892 Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. Parkinson's disease 15,056 European ancestry cases, 12,637 European ancestry controls 22,632 European ancestry cases, 968,735 European ancestry controls NR [7784415] (imputed) 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST009324 Genome-wide genotyping array 2021-06-04 31697830 Aksit MA 2019-10-19 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31697830 Genetic modifiers of cystic fibrosis-related diabetes have extensive overlap with type 2 diabetes and related traits. Cystic fibrosis-related diabetes in cystic fibrosis 1,341 European and unknown ancestry cases, 4,399 European and unknown ancestry controls 204 European and unknown ancestry cases, 387 European and unknown ancestry controls Illumina [9157530] (imputed) 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST011784 Genome-wide genotyping array 2020-04-30 31768069 Jiang L 2019-11-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31768069 A resource-efficient tool for mixed model association analysis of large-scale data. Multiple traits (2,148) 46,191 European ancestry individuals NA NR [152369] 0 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST009923 Exome-wide sequencing 2020-04-30 31768069 Jiang L 2019-11-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31768069 A resource-efficient tool for mixed model association analysis of large-scale data. Multiple traits (2,173) 456,422 European ancestry individuals NA NR [8531416] (imputed) 0 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST009924 Genome-wide genotyping array 2020-05-29 32231244 Xie J 2020-03-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32231244 The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis. Membranous nephropathy 2,150 European ancestry cases, 5,829 European ancestry controls, 1,612 East Asian ancestry cases, 1,970 East Asian ancestry controls 826 Chinese ancestry cases, 1,239 Chinese ancestry controls Illumina [~ 7000000] (imputed) 4 membranous glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004254 GCST010004 Genome-wide genotyping array 2020-05-29 32231244 Xie J 2020-03-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32231244 The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis. Membranous nephropathy 2,150 European ancestry cases, 5,829 European ancestry controls NA Illumina [~ 7000000] (imputed) 3 membranous glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004254 GCST010005 Genome-wide genotyping array 2020-05-29 32231244 Xie J 2020-03-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32231244 The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis. Membranous nephropathy 1,612 East Asian ancestry cases, 1,970 East Asian ancestry controls NA Illumina [~ 7000000] (imputed) 4 membranous glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004254 GCST010006 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Waist circumference 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 2 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST009504 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Systolic blood pressure 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 2 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST009506 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Diastolic blood pressure 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 2 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST009508 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Triglyceride levels 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST009507 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. High density lipoprotein cholesterol levels 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST009509 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Fasting blood glucose 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST009510 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Fasting blood insulin 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST009511 Genome-wide genotyping array 2020-01-27 31647587 Willems EL 2019-10-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31647587 Transethnic meta-analysis of metabolic syndrome in a multiethnic study. Weight 281 African American individuals from 73 families, 516 European American individuals from 75 families, 125 East Asian ancestry individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [3153931] (imputed) 1 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST009505 Genome-wide genotyping array 2020-06-05 32084209 Seo JY 2020-02-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/32084209 A genome-wide association study on liver enzymes in Korean population. Bilirubin levels 4,457 Korean ancestry individuals 2,031 Korean ancestry individuals Affymetrix [546738] 4 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST010048 Genome-wide genotyping array 2020-06-05 32084209 Seo JY 2020-02-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/32084209 A genome-wide association study on liver enzymes in Korean population. Serum alkaline phosphatase levels 4,457 Korean ancestry individuals 2,031 Korean ancestry individuals Affymetrix [546738] 1 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST010047 Genome-wide genotyping array 2020-06-05 32084209 Seo JY 2020-02-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/32084209 A genome-wide association study on liver enzymes in Korean population. Alanine transaminase levels 4,457 Korean ancestry individuals 2,031 Korean ancestry individuals Affymetrix [546738] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST010046 Genome-wide genotyping array 2020-06-05 32084209 Seo JY 2020-02-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/32084209 A genome-wide association study on liver enzymes in Korean population. Gamma glutamyl transferase levels 4,457 Korean ancestry individuals 2,031 Korean ancestry individuals Affymetrix [546738] 1 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST010045 Genome-wide genotyping array 2020-01-27 31681408 Yang XL 2019-10-11 Front Genet www.ncbi.nlm.nih.gov/pubmed/31681408 Three Novel Loci for Infant Head Circumference Identified by a Joint Association Analysis. Birth weight (MTAG) up to 182,902 European ancestry individuals NA NR [1977400] (imputed) 40 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST009498 Genome-wide genotyping array 2020-01-27 31681408 Yang XL 2019-10-11 Front Genet www.ncbi.nlm.nih.gov/pubmed/31681408 Three Novel Loci for Infant Head Circumference Identified by a Joint Association Analysis. Birth length (MTAG) up to 182,902 European ancestry individuals NA NR [1977400] (imputed) 27 body height at birth http://www.ebi.ac.uk/efo/EFO_0006784 GCST009499 Genome-wide genotyping array 2020-01-27 31681408 Yang XL 2019-10-11 Front Genet www.ncbi.nlm.nih.gov/pubmed/31681408 Three Novel Loci for Infant Head Circumference Identified by a Joint Association Analysis. Infant head circumference (MTAG) up to 182,902 European ancestry individuals NA NR [1977400] (imputed) 11 infant head circumference http://www.ebi.ac.uk/efo/EFO_0004577 GCST009500 Genome-wide genotyping array 2020-09-14 32572055 Sekula P 2020-06-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32572055 Urine 6-Bromotryptophan: Associations with Genetic Variants and Incident End-Stage Kidney Disease. Urine 6-bromotryptophan levels in chronic kidney disease 4,863 European ancestry individuals NA NR [9281895] (imputed) 2 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST010559 Genome-wide genotyping array 2020-08-14 32572223 Hughes DA 2020-06-22 Nat Microbiol www.ncbi.nlm.nih.gov/pubmed/32572223 Genome-wide associations of human gut microbiome variation and implications for causal inference analyses. Gut microbiota (bacterial taxa, hurdle binary method) 2,223 European ancestry individuals 1,667 European ancestry individuals Illumina [7711310] (imputed) 319 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST010396 Genome-wide genotyping array 2020-08-14 32572223 Hughes DA 2020-06-22 Nat Microbiol www.ncbi.nlm.nih.gov/pubmed/32572223 Genome-wide associations of human gut microbiome variation and implications for causal inference analyses. Gut microbiota (bacterial taxa, rank normal transformation method) 2,223 European ancestry individuals 1,667 European ancestry individuals Illumina [7711310] (imputed) 118 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST010397 Genome-wide genotyping array 2019-02-28 30677029 Riveros-McKay F 2019-01-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30677029 Genetic architecture of human thinness compared to severe obesity. Obese vs. thin 1,456 British ancestry obese children, 1,471 European ancestry thin adults up to 7,526 British ancestry obese individuals, 7,962 obese individuals, up to 3,532 British ancestry thin individuals, 8,106 thin individuals Illumina [41266535] (imputed) 14 obese body mass index status http://www.ebi.ac.uk/efo/EFO_0007041 GCST007240 Genome-wide genotyping array 2019-02-28 30677029 Riveros-McKay F 2019-01-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30677029 Genetic architecture of human thinness compared to severe obesity. Obesity (extreme) 1,456 British ancestry obese children, 6,460 European ancestry control adults up to 7,526 British ancestry obese individuals, at least 4,405 obese individuals, up to 20,720 British ancestry controls, 61,166 controls Illumina [~ 41266535] (imputed) 13 obese body mass index status http://www.ebi.ac.uk/efo/EFO_0007041 GCST007241 Genome-wide genotyping array 2019-02-28 30677029 Riveros-McKay F 2019-01-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30677029 Genetic architecture of human thinness compared to severe obesity. Normal body mass index vs. thin 1,471 European ancestry thin adults, 6,460 European ancestry control adults 3,532 British ancestry thin individuals, up to 20,720 British ancestry controls Illumina [41266535] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST007242 Genome-wide genotyping array 2020-09-23 32581250 Lin Y 2020-06-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32581250 Genome-wide association meta-analysis identifies GP2 gene risk variants for pancreatic cancer. Pancreatic cancer 2,039 Japanese ancestry cases, 32,592 Japanese ancestry controls 1,926 East Asian cases, 8,896 East Asian controls Illumina [7914378] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST010616 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Essential hypertension (time to event) 76,566 British ancestry cases, 206,305 British ancestry controls NA NR [~ 24000000] (imputed) 34 essential hypertension, age at diagnosis http://purl.obolibrary.org/obo/MONDO_0001134, http://www.ebi.ac.uk/efo/EFO_0004918 GCST010774 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Abdominal hernia (time to event) 45,957 British ancestry cases, 236,914 British ancestry controls NA NR [~ 24000000] (imputed) 0 age at diagnosis, Hernia of the abdominal wall http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/HP_0004299 GCST010773 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Hyperlipidemia (time to event) 35,623 British ancestry cases, 247,248 British ancestry controls NA NR [~ 24000000] (imputed) 2 age at diagnosis, hyperlipidemia http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0021187 GCST010772 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Osteoarthrosis (time to event) 29,071 British ancestry cases, 253,800 British ancestry controls NA NR [~ 24000000] (imputed) 5 age at diagnosis, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0005178 GCST010771 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Cardiac dysrhythmias (time to event) 25,585 British ancestry cases, 257,286 British ancestry controls NA NR [~ 24000000] (imputed) 1 age at diagnosis, cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004918, http://www.ebi.ac.uk/efo/EFO_0004269 GCST010770 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Asthma (time to event) 25,240 British ancestry cases, 257,631 British ancestry controls NA NR [~ 24000000] (imputed) 3 asthma, age at diagnosis http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0004918 GCST010769 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Cataract (time to event) 22,635 British ancestry cases, 260,236 British ancestry controls NA NR [~ 24000000] (imputed) 2 age at diagnosis, cataract http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0005129 GCST010768 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Coronary atherosclerosis (time to event) 19,079 British ancestry cases, 263,792 British ancestry controls NA NR [~ 24000000] (imputed) 5 age at diagnosis, coronary atherosclerosis http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0021661 GCST010767 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Type 2 diabetes (time to event) 18,557 British ancestry cases, 264,314 British ancestry controls NA NR [~ 24000000] (imputed) 3 age at diagnosis, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0005148 GCST010766 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Parkinson's disease (time to event) 1,345 British ancestry cases, 281,526 British ancestry controls NA NR [~ 24000000] (imputed) 0 age at diagnosis, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0005180 GCST010765 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Alzheimer's disease (time to event) 641 British ancestry cases, 282,230 British ancestry controls NA NR [~ 24000000] (imputed) 0 Alzheimer disease, age at diagnosis http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004918 GCST010764 Genome-wide genotyping array 2020-11-26 32589924 Bi W 2020-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32589924 A Fast and Accurate Method for Genome-Wide Time-to-Event Data Analysis and Its Application to UK Biobank. Schizophrenia (time to event) 551 British ancestry cases, 282,320 British ancestry controls NA NR [~ 24000000] (imputed) 0 age at diagnosis, schizophrenia http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0005090 GCST010763 Genome-wide genotyping array 2020-09-17 32627186 Man-Choi Ho A 2020-07-05 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32627186 Mood Stabilizing Antiepileptic Treatment Response in Bipolar Disorder: A Genome-Wide Association Study. Response to antiepileptic mood-stabilizing treatment in bipolar disorder 199 European ancestry cases NA Illumina [7368687] (imputed) 5 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST010579 Genome-wide genotyping array 2020-09-10 32473944 Russell AE 2020-05-28 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32473944 Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study. Suicide attempts 3,470 European ancestry cases, 150,090 European ancestry controls NA Affymetrix [at least 143006] (imputed) 15 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST010505 Genome-wide genotyping array 2020-09-10 32473944 Russell AE 2020-05-28 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32473944 Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study. Interleukin-6 levels 8,296 European ancestry individuals NA Illumina [NR] (imputed) 2 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST010504 Genome-wide genotyping array 2020-09-10 32473944 Russell AE 2020-05-28 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32473944 Investigating evidence for a causal association between inflammation and self-harm: A multivariable Mendelian Randomisation study. Deliberate self-harm 6,711 European ancestry cases, 146,849 European ancestry controls NA Affymetrix [at least 143006] (imputed) 193 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST010506 Genome-wide genotyping array 2020-09-21 32649856 Rodriguez BAT 2020-07-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32649856 A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling. Thrombin-induced platelet aggregation 1,184 European ancestry individuals NA Affymetrix [7751469] (imputed) 1 platelet aggregation http://purl.obolibrary.org/obo/GO_0070527 GCST010601 Genome-wide genotyping array 2020-09-17 32581322 Kakuta Y 2020-06-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32581322 An Integrated Genomic and Transcriptomic Analysis Reveals Candidates of Susceptibility Genes for Crohn's Disease in Japanese Populations. Crohn's disease 713 Japanese ancestry cases, 2,063 Japanese ancestry controls NA NR [7424691] (imputed) 24 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST010577 Genome-wide genotyping array 2020-07-03 32612638 Al-Khelaifi F 2020-06-16 Front Genet www.ncbi.nlm.nih.gov/pubmed/32612638 Genome-Wide Association Study Reveals a Novel Association Between MYBPC3 Gene Polymorphism, Endurance Athlete Status, Aerobic Capacity and Steroid Metabolism. World class endurance athleticism 662 European ancestry cases, 134 European ancestry controls NA Illumina [341385] 1 athletic endurance measurement http://www.ebi.ac.uk/efo/EFO_0007818 GCST010116 Targeted genotyping array [Drug-core array] 2021-06-11 32649577 Ingle JN 2020-07-08 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/32649577 Single-nucleotide polymorphism biomarkers of adjuvant anastrozole-induced estrogen suppression in early breast cancer. anastrozole induced estrone-estradiol suppression in breast cancer (high vs low) 44 high estrogen level individuals, 278 low estrogen level individuals NA Illumina [NR] 0 response to aromatase inhibitor, estradiol measurement, estrone measurement http://purl.obolibrary.org/obo/GO_0061477, http://www.ebi.ac.uk/efo/EFO_0004697, http://www.ebi.ac.uk/efo/EFO_0007970 GCST011835 Genome-wide genotyping array 2020-09-15 32580138 Shi XY 2020-06-21 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/32580138 Identification of susceptibility variants to benign childhood epilepsy with centro-temporal spikes (BECTS) in Chinese Han population. Benign childhood epilepsy with centro-temporal spikes 1,738 Han Chinese ancestry cases, 6,592 Han Chinese ancestry controls NA Illumina [5352724] (imputed) 12 Rolandic epilepsy http://www.orpha.net/ORDO/Orphanet_1945 GCST010566 Genome-wide genotyping array 2020-06-23 32366958 Woodbury-Smith MR 2020-05-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32366958 Genome-wide association study of emotional empathy in children. Emotional recognition 4,780 European ancestry children NA Illumina [27449291] (imputed) 3 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST010093 Genome-wide genotyping array 2020-06-23 32366958 Woodbury-Smith MR 2020-05-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32366958 Genome-wide association study of emotional empathy in children. Emotional recognition 2,382 European ancestry boys NA Illumina [27449291] (imputed) 8 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST010094 Genome-wide genotyping array 2020-06-23 32366958 Woodbury-Smith MR 2020-05-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32366958 Genome-wide association study of emotional empathy in children. Emotional recognition 2,393 European ancestry girls NA Illumina [27449291] (imputed) 2 facial emotion recognition measurement http://www.ebi.ac.uk/efo/EFO_0008329 GCST010095 Genome-wide genotyping array 2020-09-16 32574161 Dapas M 2020-06-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32574161 Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis. Polycystic ovary syndrome (reproductive subtype) 123 European ancestry cases, 2,964 European ancestry controls 84 European ancestry cases, 1,134 European ancestry controls Illumina [NR] (imputed) 5 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST010570 Genome-wide genotyping array 2020-09-16 32574161 Dapas M 2020-06-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32574161 Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis. Polycystic ovary syndrome (metabolic subtype) 201 European ancestry cases, 2,964 European ancestry controls 128 European ancestry cases, 1,134 European ancestry controls Illumina [NR] (imputed) 1 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST010569 Genome-wide genotyping array 2020-09-16 32574161 Dapas M 2020-06-23 PLoS Med www.ncbi.nlm.nih.gov/pubmed/32574161 Distinct subtypes of polycystic ovary syndrome with novel genetic associations: An unsupervised, phenotypic clustering analysis. Polycystic ovary syndrome (indeterminate subtype) 231 European ancestry cases, 2,964 European ancestry controls 126 European ancestry cases, 1,134 European ancestry controls Illumina [NR] (imputed) 1 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST010568 Genome-wide genotyping array 2020-09-17 32579418 Maukonen M 2020-06-24 J Biol Rhythms www.ncbi.nlm.nih.gov/pubmed/32579418 Genetic Associations of Chronotype in the Finnish General Population. Chronotype (sMEQ score) 7,436 Finnish ancestry individuals NA Illumina [5842835] (imputed) 8 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST010576 Genome-wide genotyping array 2020-09-17 32579418 Maukonen M 2020-06-24 J Biol Rhythms www.ncbi.nlm.nih.gov/pubmed/32579418 Genetic Associations of Chronotype in the Finnish General Population. Evening vs. morning chronotype (sMEQ score) 2,364 Finnish ancestry evening individuals, 5,072 Finnish ancestry morning individuals NA Illumina [5842835] (imputed) 11 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST010575 Genome-wide genotyping array 2020-09-17 32579418 Maukonen M 2020-06-24 J Biol Rhythms www.ncbi.nlm.nih.gov/pubmed/32579418 Genetic Associations of Chronotype in the Finnish General Population. Evening vs. morning chronotype (self-assessed) 3,759 Finnish ancestry evening individuals , 4,674 Finnish ancestry morning individuals NA Illumina [5842835] (imputed) 9 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST010574 Genome-wide genotyping array 2019-05-10 30664875 Cirulli ET 2019-01-18 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/30664875 A Missense Variant in PTPN22 is a Risk Factor for Drug-induced Liver Injury. Drug-induced liver injury 1,806 European ancestry cases, 133 African American cases, 109 Hispanic ancestry cases, 10,397 European ancestry controls, 1,314 African American controls, 718 Hispanic ancestry controls 113 Icelandic ancestry cases, 239,304 Icelandic ancestry controls Affymetrix, Illumina [3622749] (imputed) 0 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST007774 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CXCL6 levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 2 CXCL6 measurement http://www.ebi.ac.uk/efo/EFO_0009423 GCST90000462 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CXCL9 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CXCL9 measurement http://www.ebi.ac.uk/efo/EFO_0010780 GCST90000463 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. DNER levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 delta/notch like EGF Repeat Containing protein measurement http://www.ebi.ac.uk/efo/EFO_0010781 GCST90000464 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. EN-RAGE levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 advanced glycosylation end product-specific receptor ligand measurement http://www.ebi.ac.uk/efo/EFO_0010762 GCST90000465 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Fibroblast growth factor 19 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90000466 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Fibroblast growth factor 21 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 fibroblast growth factor 21 measurement http://www.ebi.ac.uk/efo/EFO_0010783 GCST90000467 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Fibroblast growth factor 23 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90000468 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Fibroblast growth factor 5 levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 1 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90000469 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Flt3L levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010785 GCST90000470 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Hepatocyte growth factor levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90000471 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Interleukin-10 receptor B levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 1 interleukin-10 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0010786 GCST90000472 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Interleukin-12 subunit B levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 2 interleukin 12 measurement http://www.ebi.ac.uk/efo/EFO_0004753 GCST90000473 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. interleukin 15 receptor subunit alpha levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 1 interleukin 15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008172 GCST90000474 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. interleukin-18 receptor 1 levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 2 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90000475 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Interleukin-10 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90000476 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Interleukin-18 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST90000477 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Interleukin-6 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90000478 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Interleukin-7 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 interleukin 7 measurement http://www.ebi.ac.uk/efo/EFO_0008189 GCST90000479 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Interleukin-8 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 interleukin 8 measurement http://www.ebi.ac.uk/efo/EFO_0008191 GCST90000480 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Transforming growth factor-beta levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 transforming growth factor beta measurement http://www.ebi.ac.uk/efo/EFO_0004818 GCST90000481 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Leukemia inhibitory factor receptor levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90000482 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Monocyte chemoattractant protein-1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 monocyte chemotactic protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010596 GCST90000483 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Monocyte chemoattractant protein-2 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 monocyte chemotactic protein-2 measurement http://www.ebi.ac.uk/efo/EFO_0010789 GCST90000484 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Monocyte chemoattractant protein-3 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 monocyte chemotactic protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008235 GCST90000485 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Monocyte chemoattractant protein-4 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 2 monocyte chemotactic protein-4 measurement http://www.ebi.ac.uk/efo/EFO_0010790 GCST90000486 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. 4E-BP1 levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 0 4E-BP1 measurement http://www.ebi.ac.uk/efo/EFO_0010760 GCST90000437 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Adenosine Deaminase levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 1 adenosine deaminase measurement http://www.ebi.ac.uk/efo/EFO_0010761 GCST90000438 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Axin-1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 axin-1 measurement http://www.ebi.ac.uk/efo/EFO_0010763 GCST90000439 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. beta-nerve growth factor levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST90000440 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Caspase 8 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 caspase-8 measurement http://www.ebi.ac.uk/efo/EFO_0010764 GCST90000441 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL11 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CCL11 measurement http://www.ebi.ac.uk/efo/EFO_0005188 GCST90000442 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL19 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CCL19 measurement http://www.ebi.ac.uk/efo/EFO_0009415 GCST90000443 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL20 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CCL20 measurement http://www.ebi.ac.uk/efo/EFO_0010766 GCST90000444 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL23 levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 1 CCL23 measurement http://www.ebi.ac.uk/efo/EFO_0009417 GCST90000445 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL25 levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 2 CCL25 measurement http://www.ebi.ac.uk/efo/EFO_0010768 GCST90000446 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL28 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CCL28 measurement http://www.ebi.ac.uk/efo/EFO_0010769 GCST90000447 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL3 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CCL3 measurement http://www.ebi.ac.uk/efo/EFO_0010770 GCST90000448 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CCL4 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CCL4 measurement http://www.ebi.ac.uk/efo/EFO_0004751 GCST90000449 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CD244 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CD244 measurement http://www.ebi.ac.uk/efo/EFO_0010772 GCST90000450 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CD40 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 1 CD40 measurement http://www.ebi.ac.uk/efo/EFO_0010586 GCST90000451 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CD5 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CD5 measurement http://www.ebi.ac.uk/efo/EFO_0010773 GCST90000452 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CD6 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 1 CD6 measurement http://www.ebi.ac.uk/efo/EFO_0010774 GCST90000453 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CDCP1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CUB domain containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010776 GCST90000454 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Colony stimulating factor levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 colony stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010775 GCST90000455 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Cystatin D levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 1 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90000456 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CX3CL1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CX3CL1 measurement http://www.ebi.ac.uk/efo/EFO_0009419 GCST90000457 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CXCL1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CXCL1 measurement http://www.ebi.ac.uk/efo/EFO_0010777 GCST90000458 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CXCL10 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CXCL10 measurement http://www.ebi.ac.uk/efo/EFO_0010778 GCST90000459 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CXCL11 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 CCL11 measurement http://www.ebi.ac.uk/efo/EFO_0005188 GCST90000460 Genome-wide genotyping array 2020-07-23 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. CXCL5 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 1 CXCL5 measurement http://www.ebi.ac.uk/efo/EFO_0009422 GCST90000461 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Matrix metalloproteinase levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 1 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90000487 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Matrix metalloproteinase-10 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 1 matrix metalloproteinase 10 measurement http://www.ebi.ac.uk/efo/EFO_0010589 GCST90000488 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Neurotrophin-3 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 neurotrophin-3 measurement http://www.ebi.ac.uk/efo/EFO_0010791 GCST90000489 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Osteoprotegerin levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 osteoprotegerin measurement http://www.ebi.ac.uk/efo/EFO_0005918 GCST90000490 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Oncostatin-M levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90000491 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. PD-L1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 programmed death-ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0010793 GCST90000492 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Stem cell factor levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 stem Cell Factor measurement http://www.ebi.ac.uk/efo/EFO_0008291 GCST90000493 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Sirtuin-2 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 NAD-dependent protein deacetylase sirtuin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008241 GCST90000494 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. SLAMF1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90000495 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Sulfotransferase 1A1 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 sulfotrasferase 1A1 measurement http://www.ebi.ac.uk/efo/EFO_0010797 GCST90000496 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. STAM binding protein levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 STAM binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010796 GCST90000497 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Transforming growth factor-alpha levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 transforming growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0010798 GCST90000498 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Tumor necrosis factor beta levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 3 tumor necrosis factor beta measurement http://www.ebi.ac.uk/efo/EFO_0008308 GCST90000499 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Tumor necrosis factor receptor superfamily member 9 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90000500 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Tumor necrosis factor ligand superfamily member 14 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90000501 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Tumor necrosis factor ligand superfamily member 10 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 tumor necrosis factor ligand superfamily member 10 measurement http://www.ebi.ac.uk/efo/EFO_0010800 GCST90000502 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Tumor necrosis factor ligand superfamily member 11 levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90000503 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Tumor necrosis factor ligand superfamily member 12 levels 982 Scottish ancestry individuals NA Illumina [7903493] (imputed) 1 tumor necrosis factor ligand superfamily member 12 measurement http://www.ebi.ac.uk/efo/EFO_0010801 GCST90000504 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Urokinase-type plasminogen activator levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90000505 Genome-wide genotyping array 2020-07-24 32641083 Hillary RF 2020-07-08 Genome Med www.ncbi.nlm.nih.gov/pubmed/32641083 Multi-method genome- and epigenome-wide studies of inflammatory protein levels in healthy older adults. Vascular endothelial growth factor A levels 982 Scottish ancestry individuals Illumina [7903493] (imputed) 0 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90000506 Genome-wide genotyping array 2020-09-04 32492107 Huang XF 2020-06-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/32492107 Genomewide Association Study of Acute Anterior Uveitis Identifies New Susceptibility Loci. Acute anterior uveitis in ankylosing spondylitis 2,752 European ancestry cases, 3,836 European ancestry controls NA Illumina [7436415] (imputed) 12 anterior uveitis http://www.ebi.ac.uk/efo/EFO_1000811 GCST010481 Genome-wide genotyping array 2020-06-26 25576479 Berardi C 2015-01-10 Hum Genet www.ncbi.nlm.nih.gov/pubmed/25576479 Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA). L-selectin levels 620 European ancestry individuals, 600 Chinese ancestry individuals, 579 African American individuals, 604 Hispanic individuals NA Illumina [up to 418460] 23 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST010107 Targeted genotyping array [Cardio-MetaboChip, Exome Array] 2020-09-10 32488134 Auckland K 2020-06-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32488134 The Human Leukocyte Antigen Locus and Rheumatic Heart Disease Susceptibility in South Asians and Europeans. Rheumatic heart disease 510 Northern Indian cases, 344 Northern Indian controls, 162 Fijian Indian cases, 147 Fijian Indian controls 150 European ancestry cases, 1,309 European ancestry controls Illumina [6925553] (imputed) 3 rheumatic heart disease http://www.ebi.ac.uk/efo/EFO_1001161 GCST010509 Genome-wide genotyping array 2022-10-13 32632206 Lin CW 2020-07-06 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32632206 Older molecular brain age in severe mental illness. Brain age (difference between predicted and chronological age) 165 European ancestry individuals NA Affymetrix [909622] 0 brain age measurement http://www.ebi.ac.uk/efo/EFO_0010602 GCST013016 Genome-wide genotyping array 2020-12-24 32492067 Ruffieux H 2020-06-03 PLoS Comput Biol www.ncbi.nlm.nih.gov/pubmed/32492067 A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. Protein quantitative trait loci 376 European ancestry individuals 400 European ancestry individuals Illumina [~ 4000000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST010901 Genome-wide genotyping array 2020-12-24 32492067 Ruffieux H 2020-06-03 PLoS Comput Biol www.ncbi.nlm.nih.gov/pubmed/32492067 A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. Protein quantitative trait loci 394 European ancestry individuals 548 European ancestry individuals Illumina [~ 4000000] (imputed) 78 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST010900 Genome-wide genotyping array 2020-12-24 32492067 Ruffieux H 2020-06-03 PLoS Comput Biol www.ncbi.nlm.nih.gov/pubmed/32492067 A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. Protein quantitative trait loci 400 European ancestry individuals NA Illumina [~ 4000000] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST010899 Genome-wide genotyping array 2020-12-24 32492067 Ruffieux H 2020-06-03 PLoS Comput Biol www.ncbi.nlm.nih.gov/pubmed/32492067 A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. Protein quantitative trait loci 548 European ancestry individuals NA Illumina [~ 4000000] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST010898 Genome-wide genotyping array 2020-12-24 32492067 Ruffieux H 2020-06-03 PLoS Comput Biol www.ncbi.nlm.nih.gov/pubmed/32492067 A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. Protein quantitative trait loci up to 376 European ancestry individuals up to 400 European ancestry individuals Illumina [275297] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST010897 Genome-wide genotyping array 2020-12-24 32492067 Ruffieux H 2020-06-03 PLoS Comput Biol www.ncbi.nlm.nih.gov/pubmed/32492067 A fully joint Bayesian quantitative trait locus mapping of human protein abundance in plasma. Protein quantitative trait loci up to 394 European ancestry individuals up to 548 European ancestry individuals Illumina [275485] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST010896 Genome-wide genotyping array 2020-07-20 32595297 Kweon K 2018-04-01 Soa Chongsonyon Chongsin Uihak www.ncbi.nlm.nih.gov/pubmed/32595297 Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths. Attention deficit hyperactivity disorder (inattention symptoms) 71 Korean ancestry ADHD child cases, 64 Korean ancestry child controls NA Affymetrix [525356] 2 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010221 Genome-wide genotyping array 2020-07-20 32595297 Kweon K 2018-04-01 Soa Chongsonyon Chongsin Uihak www.ncbi.nlm.nih.gov/pubmed/32595297 Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths. Attention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms) 71 Korean ancestry ADHD child cases, 64 Korean ancestry child controls NA Affymetrix [525356] 5 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010220 Genome-wide genotyping array 2020-07-20 32595297 Kweon K 2018-04-01 Soa Chongsonyon Chongsin Uihak www.ncbi.nlm.nih.gov/pubmed/32595297 Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths. Attention deficit hyperactivity disorder (inattention symptoms) 27 Korean ancestry child sibling pairs NA Affymetrix [432921] 22 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010219 Genome-wide genotyping array 2020-07-20 32595297 Kweon K 2018-04-01 Soa Chongsonyon Chongsin Uihak www.ncbi.nlm.nih.gov/pubmed/32595297 Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths. Attention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms) 27 Korean ancestry child sibling pairs NA Affymetrix [432921] 1 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010218 Genome-wide genotyping array 2020-07-20 32595297 Kweon K 2018-04-01 Soa Chongsonyon Chongsin Uihak www.ncbi.nlm.nih.gov/pubmed/32595297 Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths. Attention deficit hyperactivity disorder 71 Korean ancestry child cases, 64 Korean ancestry child controls NA Affymetrix [525356] 2 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010222 Genome-wide genotyping array 2021-03-30 33692830 Indencleef K 2021-02-22 Front Genet www.ncbi.nlm.nih.gov/pubmed/33692830 The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial Variation. Facial morphology traits (59 NSCL/P endophenotypic segments) 8,246 European ancestry individuals NA NR [7417619] (imputed) 36 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST011429 Genome-wide genotyping array 2020-09-16 32572145 Kawafune K 2020-06-22 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32572145 Strong association between the 12q24 locus and sweet taste preference in the Japanese population revealed by genome-wide meta-analysis. Sweet taste preference 12,312 Japanese ancestry individuals NA Illumina [5299861] (imputed) 13 sweet liking measurement http://www.ebi.ac.uk/efo/EFO_0010156 GCST010572 Genome-wide genotyping array 2020-09-17 32634583 Meng Y 2020-07-04 Int J Infect Dis www.ncbi.nlm.nih.gov/pubmed/32634583 Genome-wide association study identifies TPH2 variant as a novel locus for severe CV-A6-associated hand, foot, and mouth disease in Han Chinese. CV-A6-associated hand, foot, and mouth disease (severe vs mild) 115 Han Chinese ancestry severe cases, 115 Han Chinese ancestry mild controls NA Illumina [NR] 6 hand, foot and mouth disease, illness severity status http://www.ebi.ac.uk/efo/EFO_0007294, http://www.ebi.ac.uk/efo/EFO_0007863 GCST010578 Genome-wide genotyping array 2020-09-15 32564518 Ye J 2020-06-20 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/32564518 Association between herpes simplex virus 1 exposure and the risk of depression in UK Biobank. Depressive symptoms x herpes simplex 1 infection interaction 2,839 British ancestry individuals NA NR [NR] (imputed) 8 depressive symptom measurement, herpes virus seropositivity http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007036 GCST010562 Genome-wide genotyping array 2020-09-15 32564518 Ye J 2020-06-20 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/32564518 Association between herpes simplex virus 1 exposure and the risk of depression in UK Biobank. Depression x herpes simplex 1 infection interaction 1,464 British ancestry cases, 1,487 British ancestry controls NA NR [NR] (imputed) 5 unipolar depression, herpes virus seropositivity http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007036 GCST010561 Genome-wide genotyping array 2020-07-10 32121467 Adewuyi EO 2020-02-29 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/32121467 Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity. Endometriosis or migraine 17,054 European and Japanese ancestry endometriosis cases, 29,208 European ancestry migraine cases, 191,858 European and Japanese ancestry controls, 172,931 European ancestry controls NA NR [6904914] (imputed) 47 migraine disorder, endometriosis http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0001065 GCST010178 Genome-wide genotyping array 2020-10-27 32374345 Turley TN 2020-05-06 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/32374345 Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection. Spontaneous coronary artery dissection 484 European ancestry cases, 1,477 European ancestry controls 183 European ancestry cases, 340 European ancestry controls Illumina [~ 5000000] (imputed) 7 spontaneous coronary artery dissection http://www.ebi.ac.uk/efo/EFO_0010820 GCST010722 Genome-wide genotyping array 2019-03-28 30643255 Kristjansson RP 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643255 A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis. Chronic rhinosinusitis 251 European ancestry whole-genome sequenced cases, 5,357 European ancestry cases, 13,957 European ancestry whole-genome sequenced controls, 746,129 European ancestry controls NA Affymetrix, Illumina [up to 37123566] (imputed) 4 chronic rhinosinusitis http://www.ebi.ac.uk/efo/EFO_1000024 GCST007444 Genome-wide genotyping array, Genome-wide sequencing 2019-03-28 30643255 Kristjansson RP 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643255 A loss-of-function variant in ALOX15 protects against nasal polyps and chronic rhinosinusitis. Nasal polyps 86 European ancestry whole-genome sequenced cases, 4,280 European ancestry cases, 13,941 European ancestry whole-genome sequenced controls, 700,740 European ancestry controls NA Affymetrix, Illumina [up to 37123566] (imputed) 18 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST007443 Genome-wide genotyping array, Genome-wide sequencing 2020-03-02 28913729 Ruiz-Pinto S 2017-09-14 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/28913729 Exome array analysis identifies ETFB as a novel susceptibility gene for anthracycline-induced cardiotoxicity in cancer patients. Anthracycline-induced cardiotoxicity 53 European ancestry breast cancer cases, 18 European ancestry controls 52 European ancestry breast cancer cases, 31 European ancestry controls Illumina [246060] 0 response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_0005257 GCST009721 Exome genotyping array [Exome array] 2020-09-15 32573827 Huang YH 2020-06-23 Aliment Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32573827 Large-scale genome-wide association study identifies HLA class II variants associated with chronic HBV infection: a study from Taiwan Biobank. Chronic hepatitis B infection 1,810 East Asian cases, 9,002 East Asian seropositive controls 648 East Asian cases, 3,190 East Asian seropositive controls Affymetrix [583383] 2 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST010560 Genome-wide genotyping array 2021-03-19 32588970 Lutz MW 2020-06-26 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/32588970 Shared genetic etiology underlying late-onset Alzheimer's disease and posttraumatic stress syndrome. Alzheimer's disease or posttraumatic stress syndrome (pleiotropy) 21,982 LOAD cases, 41,994 controls, 2,424 European ancestry PTSD cases, 7,113 European ancestry controls, 1,968 African American LOAD cases, 2,479 African American PTSD cases, 10,672 African American controls 1011 PTSD cases, 1045 controls NR [9154389] (imputed) 0 Alzheimer disease, post-traumatic stress disorder http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0001358 GCST011300 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Sepsis (hospital admission) 4,403 European ancestry cases, 17,612 European ancestry controls NA NR [NR] 3 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST011598 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Pneumonia (28-day mortality) 513 European ancestry cases, 6,685 European ancestry controls NA NR [NR] 1 pneumonia, mortality http://www.ebi.ac.uk/efo/EFO_0003106, http://www.ebi.ac.uk/efo/EFO_0004352 GCST011597 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Pneumonia (90-day mortality) 738 European ancestry cases, 6,460 European ancestry controls NA NR [NR] 1 pneumonia, mortality http://www.ebi.ac.uk/efo/EFO_0003106, http://www.ebi.ac.uk/efo/EFO_0004352 GCST011596 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Sepsis (28-day mortality) 210 European ancestry cases, 1,827 European ancestry controls NA NR [NR] 7 Sepsis, mortality http://purl.obolibrary.org/obo/HP_0100806, http://www.ebi.ac.uk/efo/EFO_0004352 GCST011595 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Sepsis (90-day mortality) 341 European ancestry cases, 1,696 European ancestry controls NA NR [NR] 1 Sepsis, mortality http://purl.obolibrary.org/obo/HP_0100806, http://www.ebi.ac.uk/efo/EFO_0004352 GCST011594 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Infectious disease (hospital admission) 31,455 European ancestry cases, 125,820 European ancestry controls NA NR [NR] 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST011593 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Pneumonia (hospital admission) 10,472 European ancestry cases, 41,888 European ancestry controls NA NR [NR] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST011592 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Skin and soft tissue infections (hospital admission) 10,858 European ancestry cases, 43,432 European ancestry controls NA NR [NR] 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST011591 Genome-wide genotyping array 2021-04-30 32592749 Butler-Laporte G 2020-06-24 Clin Microbiol Infect www.ncbi.nlm.nih.gov/pubmed/32592749 Elevated body-mass index is associated with an increased risk of infectious disease admissions and mortality: a mendelian randomization study. Urinary tract infection (hospital admission) 13,307 European ancestry cases, 53,228 European ancestry controls NA NR [NR] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST011590 Genome-wide genotyping array 2020-07-28 29871690 Bensen JT 2018-06-05 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/29871690 A survey of microRNA single nucleotide polymorphisms identifies novel breast cancer susceptibility loci in a case-control, population-based study of African-American women. Breast cancer 3,663 African American cases, 4,687 African American controls NA Illumina [300008] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010347 Exome genotyping array [Exome array] 2020-07-07 32528159 Choquet H 2020-06-11 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32528159 A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness. Central corneal thickness 32,292 European ancestry individuals, 9,623 East Asian ancestry individuals, 1,367 Hispanic/Latino individuals, 757 African American individuals NA Affymetrix [5541230] (imputed) 74 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST90000654 Genome-wide genotyping array 2021-02-03 32641180 Steffens DC 2020-07-09 Int Psychogeriatr www.ncbi.nlm.nih.gov/pubmed/32641180 Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression. Alzheimer's disease in depression 12 European ancestry cases, 111 European ancestry controls NA Illumina [3730665] (imputed) 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST011070 Genome-wide genotyping array 2021-02-03 32641180 Steffens DC 2020-07-09 Int Psychogeriatr www.ncbi.nlm.nih.gov/pubmed/32641180 Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression. Cognitive function in depression 222 European ancestry older individuals NA Illumina [3730665] (imputed) 1 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST011069 Genome-wide genotyping array 2021-02-03 32641180 Steffens DC 2020-07-09 Int Psychogeriatr www.ncbi.nlm.nih.gov/pubmed/32641180 Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression. Cognitive impairment in depression 31 European ancestry cases, 111 European ancestry controls NA Illumina [3730665] (imputed) 1 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST011068 Genome-wide genotyping array 2021-02-03 32641180 Steffens DC 2020-07-09 Int Psychogeriatr www.ncbi.nlm.nih.gov/pubmed/32641180 Genome-wide screen to identify genetic loci associated with cognitive decline in late-life depression. Cognitive decline in depression 222 European ancestry older individuals NA Illumina [3730665] (imputed) 1 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST011067 Genome-wide genotyping array 2020-09-17 32624584 Yousaf A 2020-07-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32624584 Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder. Autism spectrum disorders (restricted interests) 2,509 individuals NA Illumina [6900500] (imputed) 0 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST010585 Genome-wide genotyping array 2020-09-17 32624584 Yousaf A 2020-07-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32624584 Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder. Autism spectrum disorders (social interaction) 2,509 individuals NA Illumina [6900500] (imputed) 4 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST010584 Genome-wide genotyping array 2020-09-17 32624584 Yousaf A 2020-07-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32624584 Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder. Autism spectrum disorders (joint attention) 2,509 individuals NA Illumina [6900500] (imputed) 0 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST010583 Genome-wide genotyping array 2020-09-17 32624584 Yousaf A 2020-07-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32624584 Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder. Autism spectrum disorders (peer interaction) 2,509 individuals NA Illumina [6900500] (imputed) 3 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST010582 Genome-wide genotyping array 2020-09-17 32624584 Yousaf A 2020-07-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32624584 Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder. Autism spectrum disorders (nonverbal communication) 2,509 individuals NA Illumina [6900500] (imputed) 0 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST010581 Genome-wide genotyping array 2020-09-17 32624584 Yousaf A 2020-07-05 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32624584 Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder. Autism spectrum disorders (repetitive sensory-motor behaviour) 2,509 individuals NA Illumina [6900500] (imputed) 4 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST010580 Genome-wide genotyping array 2020-10-08 32568366 Raghavan NS 2020-06-22 JAMA Neurol www.ncbi.nlm.nih.gov/pubmed/32568366 Association Between Common Variants in RBFOX1, an RNA-Binding Protein, and Brain Amyloidosis in Early and Preclinical Alzheimer Disease. Brain amyloid deposition (PET imaging) 4,120 Europea ancestry individuals, 89 African American individuals, 105 Hispanic individuals NA Illumina [NR] (imputed) 16 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST010650 Genome-wide genotyping array 2020-09-10 32569378 Clay-Gilmour AI 2020-06-01 Blood Adv www.ncbi.nlm.nih.gov/pubmed/32569378 Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance. Multiple myeloma 2,434 European ancestry cases, 2,705 European ancestry controls NA Affymetrix, Illumina [5864648] (imputed) 1 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST010508 Genome-wide genotyping array 2020-09-10 32569378 Clay-Gilmour AI 2020-06-01 Blood Adv www.ncbi.nlm.nih.gov/pubmed/32569378 Coinherited genetics of multiple myeloma and its precursor, monoclonal gammopathy of undetermined significance. Monoclonal gammopathy of undetermined significance 754 European ancestry cases, 879 European ancestry controls NA Illumina [5864648] (imputed) 0 monoclonal gammopathy http://www.ebi.ac.uk/efo/EFO_0000203 GCST010507 Genome-wide genotyping array 2020-09-21 32635940 Nudel R 2020-07-07 BMC Neurosci www.ncbi.nlm.nih.gov/pubmed/32635940 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study. Receptive language ability 400 European ancestry children NA Illumina [299604] 3 receptive language perception http://www.ebi.ac.uk/efo/EFO_0005686 GCST010606 Genome-wide genotyping array 2020-09-21 32635940 Nudel R 2020-07-07 BMC Neurosci www.ncbi.nlm.nih.gov/pubmed/32635940 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study. Parent of origin effect on receptive language ability (paternal) 400 European ancestry children NA Illumina [up to 299604] 12 receptive language perception, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005686, http://www.ebi.ac.uk/efo/EFO_0005939 GCST010605 Genome-wide genotyping array 2020-09-21 32635940 Nudel R 2020-07-07 BMC Neurosci www.ncbi.nlm.nih.gov/pubmed/32635940 Quantitative genome-wide association analyses of receptive language in the Danish High Risk and Resilience Study. Parent of origin effect on receptive language ability (maternal) 400 European ancestry children NA Illumina [up to 299604] 1 receptive language perception, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005686, http://www.ebi.ac.uk/efo/EFO_0005939 GCST010604 Genome-wide genotyping array 2021-02-11 32652002 Dauber A 2020-07-11 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/32652002 A Genomewide Pharmacogenetic Study of Growth Hormone Responsiveness. First year height change in growth hormone-treated short stature 504 European ancestry individuals, 88 individuals 113 Brazilian individuals Illumina [~ 2000000] (imputed) 2 response to growth hormone, height growth measurement http://www.ebi.ac.uk/efo/EFO_0010969, http://www.ebi.ac.uk/efo/EFO_0005201 GCST011107 Genome-wide genotyping array 2021-03-30 32792643 Romero-Hidalgo S 2020-08-13 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32792643 Native American ancestry significantly contributes to neuromyelitis optica susceptibility in the admixed Mexican population. Neuromyelitis optica 164 Mexican cases, 1,208 Mexican controls NA Illumina [252805] 1 neuromyelitis optica http://www.ebi.ac.uk/efo/EFO_0004256 GCST011432 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Diabetic kidney disease in diabetes 5,908 European ancestry cases, 4,967 European ancestry controls 4,579 European ancestry cases, 7,777 European ancestry controls, 7,272 Asian cases, 8,775 Asian controls, 465 Chinese ancestry cases, 154 Chinese ancestry controls, 156 Indian ancestry cases, 66 Indian ancestry controls, 202 Malay ancestry cases, 21 Malay ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 0 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST005881 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Chronic kidney disease in type 2 diabetes 3,094 European ancestry cases, 2,906 European ancestry controls 5,406 European ancestry cases, 8,744 European ancestry controls, 2,964 Asian cases, 3,323 Asian controls, 207 Chinese ancestry cases, 273 Chinese ancestry controls, 58 Indian ancestry cases, 107 Indian ancestry controls, 103 Malay ancestry cases, 56 Malay ancestry controls controls Affymetrix, Illumina [up to 9343778] (imputed) 3 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST005882 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Chronic kidney disease in diabetes 5,447 European ancestry cases, 4,717 European ancestry controls 5,406 European ancestry cases, 8,744 European ancestry controls, 2,964 Asian cases, 3,323 Asian controls, 207 Chinese ancestry cases, 273 Chinese ancestry controls, 58 Indian ancestry cases, 107 Indian ancestry controls, 103 Malay ancestry cases, 56 Malay ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 1 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST005880 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Chronic kidney disease and diabetic kidney disease in type 2 diabetes 408 European ancestry cases, 1,890 European ancestry controls 1,408 European ancestry cases, 3,840 European ancestry controls, 268 Asian cases, 632 Asian controls, 75 Chinese ancestry cases, 119 Chinese ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 4 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST005883 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Chronic kidney disease and diabetic kidney disease in diabetes 1,525 European ancestry cases, 3,908 European ancestry controls 1,408 European ancestry cases, 3,840 European ancestry controls, 268 Asian cases, 632 Asian controls, 75 Chinese ancestry cases, 119 Chinese ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 1 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST005884 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. End-stage renal disease in type 2 diabetes 371 European ancestry cases, 2,076 European ancestry controls 1,089 European ancestry cases, 5,311 European ancestry controls, 877 Asian cases, 4,861 Asian controls, 20 Chinese ancestry cases, 149 Chinese ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 2 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST005885 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. End-stage renal disease in diabetes 1,181 European ancestry cases, 4,474 European ancestry controls 1,089 European ancestry cases, 5,311 European ancestry controls, 877 Asian cases, 4,861 Asian controls, 20 Chinese ancestry cases, 149 Chinese ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST005886 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Late diabetic kidney disease in type 2 diabetes 1,339 European ancestry cases, 2,372 European ancestry controls 2,891 European ancestry cases, 6,962 European ancestry controls, 3,755 Asian cases, 10,160 Asian controls, 178 Chinese ancestry cases, 154 Chinese ancestry controls, 39 Indian ancestry cases, 64 Indian ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 4 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST005887 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Late diabetic kidney disease in diabetes 3,096 European ancestry cases, 4,967 European ancestry controls 2,891 European ancestry cases, 6,962 European ancestry controls, 3,755 Asian cases, 10,160 Asian controls, 178 Chinese ancestry cases, 154 Chinese ancestry controls, 39 Indian ancestry cases, 64 Indian ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 0 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST005888 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Early diabetic kidney disease in type 2 diabetes 1,989 European ancestry cases, 2,238 European ancestry controls 832 European ancestry cases, 2,653 European ancestry controls, 1,518 Asian cases, 3,990 Asian controls, 286 Chinese ancestry cases, 154 Chinese ancestry controls, 114 Indian ancestry cases, 66 Indian ancestry controls, 116 Malay ancestry cases, 21 Malay ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST005889 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Early diabetic kidney disease in diabetes 2,795 European ancestry cases, 4,831 European ancestry controls 832 European ancestry cases, 2,653 European ancestry controls, 1,518 Asian cases, 3,990 Asian controls, 286 Chinese ancestry cases, 154 Chinese ancestry controls, 114 Indian ancestry cases, 66 Indian ancestry controls, 116 Malay ancestry cases, 21 Malay ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 5 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST005890 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Glomerular filtration rate in type 2 diabetes 9,197 European ancestry individuals 9,333 European ancestry individuals, 7,405 Asian individuals, 975 Chinese ancestry individuals, 384 Indian ancestry individuals, 307 Malay ancestry individuals Affymetrix, Illumina [up to 9343778] (imputed) 7 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST005892 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Glomerular filtration rate in diabetes 13,158 European ancestry individuals 9,333 European ancestry individuals, 7,405 Asian individuals, 975 Chinese ancestry individuals, 384 Indian ancestry individuals, 307 Malay ancestry individuals Affymetrix, Illumina [up to 9343778] (imputed) 7 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST005891 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Diabetic kidney disease in type 2 diabetes (ESRD vs. no ESRD) 371 European ancestry cases with end-stage renal disease, 4,471 European ancestry cases without end-stage renal disease 1,640 European ancestry cases with end-stage renal disease, 7,803 European ancestry cases without end-stage renal disease, 877 Asian cases with end-stage renal disease, 4,510 Asian cases without end-stage renal disease, 20 Chinese ancestry cases with end-stage renal disease, 398 Chinese ancestry cases without end-stage renal disease Affymetrix, Illumina [up to 9343778] (imputed) 14 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST005893 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Diabetic kidney disease in diabetes (ESRD vs. no ESRD) 1,184 European ancestry cases with end-stage renal disease, 8,466 European ancestry cases without end-stage renal disease 1,640 European ancestry cases with end-stage renal disease, 7,803 European ancestry cases without end-stage renal disease, 877 Asian cases with end-stage renal disease, 4,510 Asian cases without end-stage renal disease, 20 Chinese ancestry cases with end-stage renal disease, 398 Chinese ancestry cases without end-stage renal disease Affymetrix, Illumina [up to 9343778] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST005894 Genome-wide genotyping array 2018-07-13 29703844 van Zuydam NR 2018-04-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/29703844 A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. Diabetic kidney disease in type 2 diabetes 3,345 European ancestry cases, 2,372 European ancestry controls 4,579 European ancestry cases, 7,777 European ancestry controls, 7,272 Asian cases, 8,775 Asian controls, 465 Chinese ancestry cases, 154 Chinese ancestry controls, 156 Indian ancestry cases, 66 Indian ancestry controls, 202 Malay ancestry cases, 21 Malay ancestry controls Affymetrix, Illumina [up to 9343778] (imputed) 9 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST005895 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Alzheimer's disease 212 European ancestry cases, 333 European ancestry controls 46 European ancestry cases, 257 European ancestry controls Illumina [7778465] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90013665 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Mild cognitive impairment 326 European ancestry cases, 333 European ancestry controls 448 European ancestry cases, 257 European ancestry controls Illumina [7778465] (imputed) 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90013666 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Amyloid status (abnormal vs normal) 455 European ancestry cases, 416 European ancestry controls 361 European ancestry cases, 257 European ancestry controls Illumina [7778465] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013667 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Central cerebrospinal fluid amyloid beta 42 to 40 ratio (abnormal vs normal) 418 European ancestry cases, 259 European ancestry controls NA Illumina [7778465] (imputed) 10 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013668 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Local cerebrospinal fluid amyloid beta 42 levels (abnormal vs normal) 392 European ancestry cases, 334 European ancestry controls 340 European ancestry cases, 238 European ancestry controls Illumina [7778465] (imputed) 0 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013669 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Amyloid pathology 890 European ancestry individuals 578 European ancestry individuals Illumina [7778465] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013670 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Central cerebrospinal fluid amyloid beta 42 levels 677 European ancestry individuals 578 European ancestry individuals Illumina [7778465] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013671 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Central cerebrospinal fluid amyloid beta 38 levels 675 European ancestry individuals 548 European ancestry individuals Illumina [7778465] (imputed) 0 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013672 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Central cerebrospinal fluid amyloid beta 40 levels 677 European ancestry individuals 548 European ancestry individuals Illumina [7778465] (imputed) 0 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013673 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Central cerebrospinal fluid amyloid beta 42 to 40 ratio 677 European ancestry individuals NA Illumina [7778465] (imputed) 17 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90013674 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Local cerebrospinal fluid t-tau levels (abnormal vs normal) 378 European ancestry cases, 346 European ancestry controls NA Illumina [7778465] (imputed) 0 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST90013675 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Local cerebrospinal fluid p-tau levels (abnormal vs normal) 354 European ancestry cases, 372 European ancestry controls NA Illumina [7778465] (imputed) 0 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90013676 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Cerebrospinal fluid t-tau levels 723 European ancestry individuals 571 European ancestry individuals Illumina [7778465] (imputed) 0 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST90013677 Genome-wide genotyping array 2021-02-25 33223526 Hong S 2020-11-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33223526 Genome-wide association study of Alzheimer's disease CSF biomarkers in the EMIF-AD Multimodal Biomarker Discovery dataset. Cerebrospinal fluid p-tau levels 726 European ancestry individuals 576 European ancestry individuals Illumina [7778465] (imputed) 0 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90013678 Genome-wide genotyping array 2019-05-21 30714141 Chen H 2019-02-04 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/30714141 Two novel genetic variants in the STK38L and RAB27A genes are associated with glioma susceptibility. Glioma 992 Han Chinese ancestry cases, 1,008 Han Chinese ancestry controls 2,105 Han Chinese ancestry cases, 3,374 Han Chinese ancestry controls Illumina [1889625] (imputed) 5 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST007842 Genome-wide genotyping array 2021-07-27 33232274 Mohammadnejad A 2020-11-24 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33232274 Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins. Cognitive function (kinship model) 900 Danish ancestry dizygotic twins, 272 Danish ancestry monozygotic twins NA Illumina [5779266] (imputed) 8 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012068 Genome-wide genotyping array 2021-07-27 33232274 Mohammadnejad A 2020-11-24 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33232274 Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins. Cognitive function (mixed linear model) 900 Danish ancestry dizygotic twins, 272 Danish ancestry monozygotic twins NA Illumina [5779266] (imputed) 8 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012067 Genome-wide genotyping array 2021-07-27 33232274 Mohammadnejad A 2020-11-24 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33232274 Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins. Cognitive function (generalized correlation coefficient) 278 Chinese ancestry dizygotic twins NA Illumina [5432814] (imputed) 28 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012066 Genome-wide genotyping array 2021-07-27 33232274 Mohammadnejad A 2020-11-24 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33232274 Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins. Cognitive function (kinship model) 278 Chinese ancestry dizygotic twins NA Illumina [5432814] (imputed) 8 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012065 Genome-wide genotyping array 2021-07-27 33232274 Mohammadnejad A 2020-11-24 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33232274 Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins. Cognitive function (mixed linear model) 278 Chinese ancestry dizygotic twins NA Illumina [5432814] (imputed) 9 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012064 Genome-wide genotyping array 2021-07-27 33232274 Mohammadnejad A 2020-11-24 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33232274 Generalized correlation coefficient for genome-wide association analysis of cognitive ability in twins. Cognitive function (generalized correlation coefficient) 900 Danish ancestry dizygotic twins, 272 Danish ancestry monozygotic twins NA Illumina [5779266] (imputed) 30 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012069 Genome-wide genotyping array 2019-03-19 30718901 Howard DM 2019-02-04 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/30718901 Genome-wide meta-analysis of depression identifies 102 independent variants and highlights the importance of the prefrontal brain regions. Depression 118,811 European ancestry cases, 327,427 European ancestry controls, 127,552 cases, 233,763 controls 414,055 European ancestry cases, 892,299 European ancestry controls NR [8098588] (imputed) 98 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST007342 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. same-sex sexual behaviour 329,546 European ancestry males 2,196 European ancestry males, up to 9,109 European ancestry twins Affymetrix, Illumina [NR] (imputed) 0 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008652 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. same-sex sexual behaviour 338,218 European ancestry females 2,529 European ancestry females, up to 9,109 European ancestry twins Affymetrix, Illumina [NR] (imputed) 0 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008653 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. same-sex sexual behaviour 329,546 European ancestry males, 338,218 European ancestry females 2,196 European ancestry males, 2,529 European ancestry females, 9,109European ancestry twins Affymetrix, Illumina [NR] (imputed) 0 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008654 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. proportion of same-sex sexual behaviour among non-heterosexuals 7,675 European ancestry males NA Affymetrix, Illumina [NR] (imputed) 0 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008655 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. proportion of same-sex sexual behaviour among non-heterosexuals 5,838 European ancestry females NA Affymetrix, Illumina [NR] (imputed) 0 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008656 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. proportion of same-sex sexual behaviour among non-heterosexuals at least 7,675 European ancestry males, at least 5,838 European ancestry females NA Affymetrix, Illumina [NR] (imputed) 0 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008657 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. same-sex sexual behaviour 188,825 European ancestry males NA Affymetrix [NR] (imputed) 2 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008649 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. same-sex sexual behaviour 220,170 European ancestry females NA Affymetrix [NR] (imputed) 0 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008650 Genome-wide genotyping array 2019-09-13 31467194 Ganna A 2019-08-01 Science www.ncbi.nlm.nih.gov/pubmed/31467194 Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. same-sex sexual behaviour 188,825 European ancestry males, 220,170 European ancestry females NA Affymetrix [NR] (imputed) 2 same-sex sexual behavior http://www.ebi.ac.uk/efo/EFO_0010142 GCST008651 Genome-wide genotyping array 2019-09-04 31374203 Lam M 2019-08-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31374203 Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. Cognitive ability, years of educational attainment or schizophrenia (pleiotropy) 328,917 individuals with educational attainment measurements, 107,207 individuals with cognitive ability measurements, 77,096 European ancestry schizophrenia cases, 43,456 European ancestry controls NA NR [7306098] 235 schizophrenia, intelligence, self reported educational attainment http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0004784 GCST008595 Genome-wide genotyping array 2022-08-25 31316127 Mao XJ 2019-07-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31316127 Improved detection of common variants in coronary artery disease and blood pressure using a pleiotropy cFDR method. Coronary artery disease and systolic blood pressure (pleiotropy) 69,395 European ancestry individuals with blood pressure measurements, 22,233 European ancestry coronary artery disease cases, 64,762 European ancestry controls 8,424 European ancestry coronary artery disease cases, 6,996 South Asian ancestry coronary artery disease cases, 7,268 European ancestry controls, 7,794 South Asian ancestry controls NR [NR] 0 systolic blood pressure, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0001645 GCST012937 Genome-wide genotyping array 2022-08-25 31316127 Mao XJ 2019-07-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31316127 Improved detection of common variants in coronary artery disease and blood pressure using a pleiotropy cFDR method. Coronary artery disease and diastolic blood pressure (pleiotropy) 69,395 European ancestry individuals with blood pressure measurements, 22,233 European ancestry coronary artery disease cases, 64,762 European ancestry controls 8,424 European ancestry coronary artery disease cases, 6,996 South Asian ancestry coronary artery disease cases, 7,268 European ancestry controls, 7,794 South Asian ancestry controls NR [NR] 0 diastolic blood pressure, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0001645 GCST012936 Genome-wide genotyping array 2019-09-16 31367044 Locke AE 2019-07-31 Nature www.ncbi.nlm.nih.gov/pubmed/31367044 Exome sequencing of Finnish isolates enhances rare-variant association power. Cardiometabolic traits up to 19,292 Finnish ancestry individuals 24,776 Finnish ancestry individuals NR [at least 1318781] 0 ketone body measurement, alcohol consumption measurement, body mass index, linoleic acid measurement, glycerophospholipid measurement, fatty acid measurement, glomerular filtration rate, insulin measurement, BMI-adjusted fasting blood glucose measurement, body fat percentage, glutamine measurement, lipoprotein measurement, glycine measurement, 3-hydroxybutyric acid measurement, body height, pulse pressure measurement, leucine measurement, hip circumference, serum albumin measurement, valine measurement, waist circumference, omega-3 polyunsaturated fatty acid measurement, sphingomyelin measurement, total cholesterol measurement, C-reactive protein measurement, adiponectin measurement, high density lipoprotein cholesterol measurement, phenylalanine measurement, creatinine measurement, systolic blood pressure, histidine measurement, body weight, glucose measurement, vitamin D measurement, docosahexaenoic acid measurement, acetoacetate measurement, tyrosine measurement, isoleucine measurement, omega-6 polyunsaturated fatty acid measurement, acetate measurement, pyruvate measurement, waist-hip ratio, citrate measurement, alanine measurement, diastolic blood pressure, triglyceride measurement, very low density lipoprotein cholesterol measurement, glycoprotein measurement, low density lipoprotein cholesterol measurement, apolipoprotein A 1 measurement, fasting blood insulin measurement, intermediate density lipoprotein measurement, apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0010110, http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0006807, http://www.ebi.ac.uk/efo/EFO_0007630, http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0004467, http://www.ebi.ac.uk/efo/EFO_0008036, http://www.ebi.ac.uk/efo/EFO_0007800, http://www.ebi.ac.uk/efo/EFO_0009768, http://www.ebi.ac.uk/efo/EFO_0004732, http://www.ebi.ac.uk/efo/EFO_0009767, http://www.ebi.ac.uk/efo/EFO_0010113, http://www.ebi.ac.uk/efo/EFO_0004339, http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009770, http://www.ebi.ac.uk/efo/EFO_0005093, http://www.ebi.ac.uk/efo/EFO_0004535, http://www.ebi.ac.uk/efo/EFO_0009792, http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0010119, http://www.ebi.ac.uk/efo/EFO_0010118, http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0004502, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0005001, http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0009769, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004468, http://www.ebi.ac.uk/efo/EFO_0004631, http://www.ebi.ac.uk/efo/EFO_0007761, http://www.ebi.ac.uk/efo/EFO_0010111, http://www.ebi.ac.uk/efo/EFO_0005058, http://www.ebi.ac.uk/efo/EFO_0009793, http://www.ebi.ac.uk/efo/EFO_0005680, http://www.ebi.ac.uk/efo/EFO_0010112, http://www.ebi.ac.uk/efo/EFO_0010117, http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0010114, http://www.ebi.ac.uk/efo/EFO_0009765, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004555, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004614, http://www.ebi.ac.uk/efo/EFO_0004466, http://www.ebi.ac.uk/efo/EFO_0008595, http://www.ebi.ac.uk/efo/EFO_0004615 GCST008673 Exome-wide sequencing 2021-02-26 33563987 Tyrrell J 2021-02-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33563987 Genetic predictors of participation in optional components of UK Biobank. Percentage of invited food questionnaires completed 300,639 European ancestry individuals NA Affymetrix [39302896] (imputed) 13 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90012790 Genome-wide genotyping array 2021-02-26 33563987 Tyrrell J 2021-02-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33563987 Genetic predictors of participation in optional components of UK Biobank. Acceptance of an invitation to wear a physical activity monitor 96,035 European ancestry cases, 119,092 European ancestry controls NA Affymetrix [39302896] (imputed) 2 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90012791 Genome-wide genotyping array 2021-02-26 33563987 Tyrrell J 2021-02-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33563987 Genetic predictors of participation in optional components of UK Biobank. Acceptance of an invitation to participate in a mental health questionnaire 146,074 European ancestry cases, 148,713 European ancestry controls NA Affymetrix [39302896] (imputed) 41 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90012792 Genome-wide genotyping array 2021-02-26 33563987 Tyrrell J 2021-02-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33563987 Genetic predictors of participation in optional components of UK Biobank. Completion of the aide-memoire 361,501 European ancestry cases, 89,535 European ancestry controls NA Affymetrix [39302896] (imputed) 5 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90012793 Genome-wide genotyping array 2021-02-26 33563987 Tyrrell J 2021-02-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33563987 Genetic predictors of participation in optional components of UK Biobank. Participation in an health questionnaire (not invited vs invited) 336,633 European ancestry cases, 114,464 European ancestry controls NA Affymetrix [39302896] (imputed) 36 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90012794 Genome-wide genotyping array 2019-08-27 28972577 Hancock DB 2017-10-03 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28972577 Genome-wide association study across European and African American ancestries identifies a SNP in DNMT3B contributing to nicotine dependence. Nicotine dependence 28,677 European ancestry individuals, 9,925 African American individuals NA Affymetrix, Illumina [~ 18000000] (imputed) 6 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST008496 Genome-wide genotyping array 2021-03-30 32772156 Muntane G 2020-08-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32772156 The shared genetic architecture of schizophrenia, bipolar disorder and lifespan. Schizophrenia or parental lifespan (pleiotropy) 40,675 European ancestry cases, 64,643 European ancestry controls, 450,000 European ancestry individuals NA NR [3206698] (imputed) 0 parental longevity, schizophrenia http://www.ebi.ac.uk/efo/EFO_0007796, http://purl.obolibrary.org/obo/MONDO_0005090 GCST011430 Genome-wide genotyping array 2021-03-30 32772156 Muntane G 2020-08-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32772156 The shared genetic architecture of schizophrenia, bipolar disorder and lifespan. Bipolar disorder or parental lifespan (pleiotropy) 20,352 European ancestry cases, 31,358 European ancestry controls, 450,000 European ancestry individuals NA NR [3206698] (imputed) 0 parental longevity, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0007796, http://purl.obolibrary.org/obo/MONDO_0004985 GCST011431 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (forehead protrusion 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST90026537 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (forehead protrusion 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST90026538 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (forehead size 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST90026539 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (forehead size 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST90026540 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (brow ridge protrusion 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 7 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026541 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (brow ridge protrusion 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026542 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (eye size 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90026543 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (eye size 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90026544 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nasion depth 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026545 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nasion depth 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026546 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nasion position 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026547 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nasion position 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026548 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (eye position 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90026549 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (eye position 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90026550 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose height) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026551 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose protrusion) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026552 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose size) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026553 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose roundness 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 8 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026554 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose roundness 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026555 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose roundness 3) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 5 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026556 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose curvature 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026557 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose curvature 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026558 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nose curvature 3) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026559 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (columella inclination) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 9 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026560 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nostril inclination) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026561 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (nostril size) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026562 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (columella size) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 4 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90026563 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip thickness 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026564 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip thickness 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026565 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip thickness 3) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026566 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (upper lip thickness 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026567 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lower lip thickness 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026568 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (upper lip thickness 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026569 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lower lip thickness 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026570 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip thickness ratio 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026571 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip thickness ratio 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026572 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (upper lip protrusion) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026573 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lower lip protrusion) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026574 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip protrusion) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026575 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip width 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026576 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lip width 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90026577 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (philtrum length) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026578 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (chin protrusion 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90026579 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (chin protrusion 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90026580 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (ear size) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 outer ear morphology trait http://www.ebi.ac.uk/efo/EFO_0007664 GCST90026581 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (ear inclination) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 outer ear morphology trait http://www.ebi.ac.uk/efo/EFO_0007664 GCST90026582 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (jaw protrusion 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026583 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (jaw protrusion 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026584 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (jaw protrusion 3) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026585 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (jaw protrusion 4) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026586 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (jaw protrusion 5) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026587 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (jaw slope 1) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026588 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (chin roundness) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90026589 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (jaw slope 2) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026590 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (upper face flatness) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90026591 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (face flatness) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026592 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (brow ridge protrusion 3) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 3 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026593 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (mid face flatness) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90026594 Genome-wide genotyping array 2021-08-25 33547071 Bonfante B 2021-02-05 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33547071 A GWAS in Latin Americans identifies novel face shape loci, implicating VPS13B and a Denisovan introgressed region in facial variation. Facial morphology (lower face flatness) 6,169 Latin American individuals NA Illumina [8703729] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90026595 Genome-wide genotyping array 2021-08-13 33527407 Truong T 2021-02-02 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/33527407 Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium. Differentiated thyroid cancer 1,554 European ancestry cases, 1,973 European ancestry controls 2,229 European ancestry cases, 2,059 European ancestry controls Illumina [9673063] (imputed) 8 differentiated thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_1002017 GCST012197 Genome-wide genotyping array 2021-08-13 33527407 Truong T 2021-02-02 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/33527407 Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium. Differentiated thyroid cancer 301 Oceanian ancestry cases, 348 Oceanian ancestry controls NA Illumina [7179638] (imputed) 0 differentiated thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_1002017 GCST012196 Genome-wide genotyping array 2021-08-13 33527407 Truong T 2021-02-02 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/33527407 Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium. Differentiated thyroid cancer 1,554 European ancestry cases, 1,973 European ancestry controls, 301 Oceanian ancestry cases, 348 Oceanian ancestry controls NA Illumina [6479975] (imputed) 11 differentiated thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_1002017 GCST012195 Genome-wide genotyping array 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Blood cell traits (multivariate analysis) up to 6,407 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 8 lymphocyte count, mean platelet volume, leukocyte count, mean corpuscular volume, hematocrit, obsolete_red blood cell distribution width, basophil count, platelet count, neutrophil count, hemoglobin measurement, erythrocyte count, mean corpuscular hemoglobin concentration, monocyte count, mean corpuscular hemoglobin, eosinophil count http://www.ebi.ac.uk/efo/EFO_0004587, http://www.ebi.ac.uk/efo/EFO_0004584, http://www.ebi.ac.uk/efo/EFO_0004308, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0005192, http://www.ebi.ac.uk/efo/EFO_0005090, http://www.ebi.ac.uk/efo/EFO_0004309, http://www.ebi.ac.uk/efo/EFO_0004833, http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528, http://www.ebi.ac.uk/efo/EFO_0005091, http://www.ebi.ac.uk/efo/EFO_0004527, http://www.ebi.ac.uk/efo/EFO_0004842 GCST008338 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. White blood cell count 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST008322 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Red blood cell count 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 2 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST008329 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Mean corpuscular volume 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 1 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST008330 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Mean corpuscular hemoglobin 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 1 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST008331 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Mean corpuscular hemoglobin concentration 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 1 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST008332 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Red cell distribution width 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 1 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST008333 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Hematocrit 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST008323 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Hemoglobin 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST008324 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Neutrophil count 1,415 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 1 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST008334 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Platelet count 1,625 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST008325 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Lymphocyte count 1,565 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST008326 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Monocyte count 1,565 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST008327 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Basophil count 1,565 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST008328 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Eosinophil counts 1,555 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 2 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST008335 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Mean platelet volume 1,624 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 2 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST008336 Genome-wide genotyping array, Genome-wide sequencing 2019-08-02 31080455 Fatumo S 2019-04-26 Front Genet www.ncbi.nlm.nih.gov/pubmed/31080455 Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Blood cell traits (multivariate analysis) up to 6,407 Sub-Saharan African ancestry individuals NA Illumina [20594536] (imputed) 3 neutrophil count, mean platelet volume, leukocyte count, erythrocyte count, mean corpuscular hemoglobin concentration, mean corpuscular volume, monocyte count, obsolete_red blood cell distribution width, basophil count, platelet count, eosinophil count http://www.ebi.ac.uk/efo/EFO_0004833, http://www.ebi.ac.uk/efo/EFO_0004584, http://www.ebi.ac.uk/efo/EFO_0004308, http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0005091, http://www.ebi.ac.uk/efo/EFO_0005192, http://www.ebi.ac.uk/efo/EFO_0005090, http://www.ebi.ac.uk/efo/EFO_0004309, http://www.ebi.ac.uk/efo/EFO_0004842 GCST008337 Genome-wide genotyping array, Genome-wide sequencing 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Urine specific gravity measurement 139,555 Icelandic ancestry individuals (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 0 urine specific gravity measurement http://www.ebi.ac.uk/efo/EFO_0010135 GCST008604 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Glucosuria (moderate to severe) 6,109 Icelandic ancestry cases, 135,512 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 7 Glycosuria http://purl.obolibrary.org/obo/HP_0003076 GCST008605 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Glucosuria (mild) 4,748 Icelandic ancestry cases, 135,512 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 3 Glycosuria http://purl.obolibrary.org/obo/HP_0003076 GCST008606 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Ketonuria 41,130 Icelandic ancestry cases, 95,568 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 1 Ketonuria http://purl.obolibrary.org/obo/HP_0002919 GCST008607 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Ketonuria (moderate to severe) 21,803 Icelandic ancestry cases, 95,568 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 1 Ketonuria http://purl.obolibrary.org/obo/HP_0002919 GCST008608 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Ketonuria (mild) 19,327 Icelandic ancestry cases, 95,568 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 1 Ketonuria http://purl.obolibrary.org/obo/HP_0002919 GCST008609 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Proteinuria 54,009 Icelandic ancestry cases, 91,538 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 2 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST008610 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Proteinuria (moderate to severe) 25,317 Icelandic ancestry cases, 91,538 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 2 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST008611 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Proteinuria (mild) 28,692 Icelandic ancestry cases, 91,538 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 2 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST008612 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Hematuria 68,051 Icelandic ancestry cases, 68,903 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 4 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST008613 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Hematuria (moderate to severe) 49,212 Icelandic ancestry cases, 68,903 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 4 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST008617 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Hematuria (mild) 18,839 Icelandic ancestry cases, 68,903 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 2 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST008618 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Urine pH measurement 149,899 Icelandic ancestry individuals (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 4 urinary pH measurement http://www.ebi.ac.uk/efo/EFO_0010136 GCST008616 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Low urine pH 35,897 Icelandic ancestry cases, 112,302 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 4 urinary pH measurement http://www.ebi.ac.uk/efo/EFO_0010136 GCST008615 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Signs of urinary tract infection (nitrites and leukocyte esterase) 13,322 Icelandic ancestry cases, 66,528 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 0 leukocyte esterase measurement, nitrite measurement http://www.ebi.ac.uk/efo/EFO_0010137, http://www.ebi.ac.uk/efo/EFO_0010138 GCST008619 Genome-wide genotyping array 2019-09-05 30476138 Benonisdottir S 2019-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30476138 Sequence variants associating with urinary biomarkers. Glucosuria 10,857 Icelandic ancestry cases, 135,512 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32500000] (imputed) 8 Glycosuria http://purl.obolibrary.org/obo/HP_0003076 GCST008614 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Bitter alcoholic beverage consumption 336,448 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 97 bitter alcoholic beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010092 GCST008522 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Bitter non-alcoholic beverage consumption 85,852 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 23 bitter non-alcoholic beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010093 GCST008524 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Coffee consumption 335,909 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 87 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST008526 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Tea consumption 336,898 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 63 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST008529 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Grapefruit juice consumption 85,852 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 4 grapefruit juice consumption measurement http://www.ebi.ac.uk/efo/EFO_0010094 GCST008531 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Sweet beverage consumption 85,852 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 7 sweet beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010090 GCST008528 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Sugar-sweetened beverage consumption 85,852 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 1 sugar sweetened beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010097 GCST008527 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Artificially sweetened beverage consumption 85,852 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 4 artificially sweetened beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010096 GCST008525 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Pure non-grapefruit juice consumption 85,852 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 2 non-grapefruit juice consumption measurement http://www.ebi.ac.uk/efo/EFO_0010095 GCST008523 Genome-wide genotyping array 2019-08-29 31046077 Zhong VW 2019-05-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31046077 A genome-wide association study of bitter and sweet beverage consumption. Bitter beverage consumption 85,852 European ancestry individuals 39,924 European ancestry individuals Affymetrix [~ 7740000] (imputed) 27 bitter beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010089 GCST008521 Genome-wide genotyping array 2019-02-01 30566433 Taira M 2018-12-19 PLoS One www.ncbi.nlm.nih.gov/pubmed/30566433 A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes. Type 2 diabetes nephropathy 2,809 Japanese ancestry cases, 5,592 Japanese ancestry controls 2,115 Japanese ancestry cases, 2,519 Japanese ancestry controls Illumina [5768242] (imputed) 6 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST007021 Genome-wide genotyping array 2019-02-01 30566433 Taira M 2018-12-19 PLoS One www.ncbi.nlm.nih.gov/pubmed/30566433 A variant within the FTO confers susceptibility to diabetic nephropathy in Japanese patients with type 2 diabetes. Type 2 diabetes nephropathy including microalbuminuria at least 2,809 Japanese ancestry cases, 5,592 Japanese ancestry controls at least 2,115 Japanese ancestry cases, 2,519 Japanese ancestry controls Illumina [NR] 6 Moderate albuminuria, diabetic nephropathy http://purl.obolibrary.org/obo/HP_0012594, http://www.ebi.ac.uk/efo/EFO_0000401 GCST007022 Genome-wide genotyping array 2019-02-08 30566500 Day F 2018-12-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30566500 Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria. Polycystic ovary syndrome 10,074 European ancestry cases, 103,164 European ancestry controls NA Illumina [> 10000000] (imputed) 14 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST007089 Genome-wide genotyping array 2019-02-13 30237584 El Rouby N 2018-09-20 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30237584 Genome-wide association analysis of common genetic variants of resistant hypertension. Resistant hypertension 297 European ancestry cases, 226 Hispanic cases, 623 European ancestry controls, 633 Hispanic controls 1,946 European ancestry cases, 471 European ancestry controls Illumina [NR] 4 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST007135 Genome-wide genotyping array 2019-02-13 30237584 El Rouby N 2018-09-20 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30237584 Genome-wide association analysis of common genetic variants of resistant hypertension. Resistant hypertension 226 European ancestry cases, 143 Hispanic cases, 431 European ancestry controls, 394 Hispanic controls 71 European ancestry cases, 83 Hispanic cases, 192 European ancestry controls, 239 Hispanic controls Illumina [696317] 3 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST007136 Genome-wide genotyping array 2019-08-20 31311600 Namjou B 2019-07-17 BMC Med www.ncbi.nlm.nih.gov/pubmed/31311600 GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Nonalcoholic fatty liver disease 1,106 European ancestry cases, 8,571 European ancestry controls NA NR [7263501] (imputed) 16 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST008468 Genome-wide genotyping array 2019-08-20 31311600 Namjou B 2019-07-17 BMC Med www.ncbi.nlm.nih.gov/pubmed/31311600 GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease 235 European ancestry individuals NA NR [7263501] (imputed) 16 non-alcoholic fatty liver disease severity measurement http://www.ebi.ac.uk/efo/EFO_0008421 GCST008471 Genome-wide genotyping array 2019-08-20 31311600 Namjou B 2019-07-17 BMC Med www.ncbi.nlm.nih.gov/pubmed/31311600 GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Liver fibrosis in non-alcoholic fatty liver disease 235 European ancestry individuals NA NR [7263501] (imputed) 17 Hepatic fibrosis http://purl.obolibrary.org/obo/HP_0001395 GCST008469 Genome-wide genotyping array 2019-08-20 31311600 Namjou B 2019-07-17 BMC Med www.ncbi.nlm.nih.gov/pubmed/31311600 GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Aspartate aminotransferase levels in non-alcoholic fatty liver disease 1,075 European ancestry individuals NA NR [7263501] (imputed) 17 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST008467 Genome-wide genotyping array 2019-08-20 31311600 Namjou B 2019-07-17 BMC Med www.ncbi.nlm.nih.gov/pubmed/31311600 GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Alanine aminotransferase levels in non-alcoholic fatty liver disease 1,075 European ancestry individuals NA NR [7263501] (imputed) 19 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST008466 Genome-wide genotyping array 2019-08-20 31311600 Namjou B 2019-07-17 BMC Med www.ncbi.nlm.nih.gov/pubmed/31311600 GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Nonalcoholic fatty liver disease (SNP x SNP interaction) 1,106 European ancestry cases, 8,571 European ancestry controls NA NR [7263501] (imputed) 1 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST008470 Genome-wide genotyping array 2020-08-19 32493714 Klimentidis YC 2020-06-03 Diabetes www.ncbi.nlm.nih.gov/pubmed/32493714 Phenotypic and Genetic Characterization of Lower LDL-C and Increased Type-2 Diabetes Risk in the UK Biobank. Low density lipoprotein cholesterol levels 431,167 European ancestry individuals NA Affymetrix [15000001] 157 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90002412 Genome-wide genotyping array 2021-05-04 32963231 Hofer E 2020-09-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32963231 Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Cortical surface area 18,617 European and African American ancestry individuals 22,363 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 41 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST011617 Genome-wide genotyping array 2021-05-04 32963231 Hofer E 2020-09-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32963231 Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Cortical volume 22,824 European and African American ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 62 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST011616 Genome-wide genotyping array 2021-05-04 32963231 Hofer E 2020-09-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32963231 Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults. Cortical thickness 22,163 European and African American ancestry individuals 22,363 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 12 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST011618 Genome-wide genotyping array 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Carboplatin drug response (IC50) 168 European ancestry individuals NA NR [6315985] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011787 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Ara-C drug response (AUC) 432 East Asian, European and African ancestry individuals NA NR [3799865] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011773 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Capecitabine drug response (AUC) 424 East Asian, European and African ancestry individuals NA NR [3799863] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011774 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Carboplatin drug response (IC50) 430 East Asian, European and African ancestry individuals NA NR [3799860] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011775 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Cisplatin drug response (IC50) 431 East Asian, European and African ancestry individuals NA NR [3799860] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011776 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Daunorubicin drug response (IC50) 259 European and African ancestry individuals NA NR [3798360] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011777 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Etoposide drug response (IC50) 255 European and African ancestry individuals NA NR [3798298] (imputed) 1 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011778 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Paclitaxel drug response (AUC) 164 European and African ancestry individuals NA NR [3796783] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011779 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Pemetrexed drug response (AUC) 260 European and African ancestry individuals NA NR [3798359] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011780 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Ara-C drug response (AUC) 90 East Asian ancestry individuals NA NR [5206187] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011781 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Capecitabine drug response (AUC) 84 East Asian ancestry individuals NA NR [5200691] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011782 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Carboplatin drug response (IC50) 90 East Asian ancestry individuals NA NR [5206187] (imputed) 1 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011783 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Cisplatin drug response (IC50) 90 East Asian ancestry individuals NA NR [5206187] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011784 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Ara-C drug response (AUC) 165 European ancestry individuals NA NR [6310542] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011785 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Capecitabine drug response (AUC) 165 European ancestry individuals NA NR [6311590] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011786 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Cisplatin drug response (IC50) 166 European ancestry individuals NA NR [6312355] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011788 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Daunorubicin drug response (IC50) 86 European ancestry individuals NA NR [6263189] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011789 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Etoposide drug response (IC50) 84 European ancestry individuals NA NR [6255207] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011790 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Paclitaxel drug response (AUC) 77 European ancestry individuals NA NR [6223077] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011791 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Pemetrexed drug response (AUC) 84 European ancestry individuals NA NR [6254701] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011792 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Ara-C drug response (AUC) 177 African ancestry individuals NA NR [9548582] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011793 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Capecitabine drug response (AUC) 175 African ancestry individuals NA NR [9542312] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011794 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Carboplatin drug response (IC50) 172 African ancestry individuals NA NR [9531231] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011795 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Cisplatin drug response (IC50) 175 African ancestry individuals NA NR [9542566] (imputed) 1 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011796 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Daunorubicin drug response (IC50) 173 African ancestry individuals NA NR [9536189] (imputed) 1 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011797 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Etoposide drug response (IC50) 171 African ancestry individuals NA NR [9524322] (imputed) 1 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011798 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Paclitaxel drug response (AUC) 87 African ancestry individuals NA NR [9364915] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011799 Genome-wide genotyping array, Genome-wide sequencing 2021-02-23 33575800 Mulford AJ 2021-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33575800 Genetically regulated expression underlies cellular sensitivity to chemotherapy in diverse populations. Pemetrexed drug response (AUC) 176 African ancestry individuals NA NR [9545800] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90011800 Genome-wide genotyping array, Genome-wide sequencing 2019-08-07 31066027 Nicoletti P 2019-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31066027 Shared genetic risk factors across carbamazepine-induced hypersensitivity reactions. Carbamazepine-induced liver injury 12 European ancestry cases, 8,438 European ancestry controls NA Illumina [5271349] (imputed) 0 drug-induced liver injury, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0004228, http://www.ebi.ac.uk/efo/EFO_0008484 GCST008383 Genome-wide genotyping array 2019-08-07 31066027 Nicoletti P 2019-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31066027 Shared genetic risk factors across carbamazepine-induced hypersensitivity reactions. Carbamazepine-induced reaction with eosinophilia and systemic symptoms 25 European ancestry cases, 10,701 European ancestry controls NA Illumina [5271349] (imputed) 3 drug hypersensitivity syndrome, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_1002004, http://www.ebi.ac.uk/efo/EFO_0008484 GCST008384 Genome-wide genotyping array 2019-08-07 31066027 Nicoletti P 2019-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31066027 Shared genetic risk factors across carbamazepine-induced hypersensitivity reactions. Carbamazepine-induced Stevens-Johnson syndrome or toxic epidermal necrolysis (SJS/TEN) 16 European ancestry cases, 8,438 European ancestry controls NA Illumina [5271349] (imputed) 0 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://www.ebi.ac.uk/efo/EFO_0008484 GCST008385 Genome-wide genotyping array 2019-08-07 31066027 Nicoletti P 2019-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31066027 Shared genetic risk factors across carbamazepine-induced hypersensitivity reactions. Carbamazepine-induced serious cutaneous adverse reaction 43 European ancestry cases, 10,701 European ancestry controls NA Illumina [5271349] (imputed) 3 severe cutaneous adverse reaction, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0006346, http://www.ebi.ac.uk/efo/EFO_0008484 GCST008386 Genome-wide genotyping array 2020-07-28 32450446 Wang H 2020-04-29 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/32450446 Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease. Neuritic plaques (SNP x SNP interaction) 1,316 individuals NA Affymetrix, Illumina [279409] (imputed) 93 neuritic plaque measurement http://www.ebi.ac.uk/efo/EFO_0006798 GCST010342 Genome-wide genotyping array 2020-07-28 32450446 Wang H 2020-04-29 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/32450446 Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease. Diffuse plaques (SNP x SNP interaction) 1,316 individuals NA Affymetrix, Illumina [279409] (imputed) 275 diffuse plaque measurement http://www.ebi.ac.uk/efo/EFO_0010699 GCST010341 Genome-wide genotyping array 2020-07-28 32450446 Wang H 2020-04-29 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/32450446 Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease. Total PHF-tau (SNP x SNP interaction) 1,285 individuals NA Affymetrix, Illumina [279409] (imputed) 1584 PHF-tau measurement http://www.ebi.ac.uk/efo/EFO_0010750 GCST010340 Genome-wide genotyping array 2020-07-28 32450446 Wang H 2020-04-29 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/32450446 Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease. Total amyloid (SNP x SNP interaction) 1,276 individuals NA Affymetrix, Illumina [279409] (imputed) 96 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST010339 Genome-wide genotyping array 2020-07-28 32450446 Wang H 2020-04-29 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/32450446 Genome-wide interaction analysis of pathological hallmarks in Alzheimer's disease. Neurofibrillary tangles (SNP x SNP interaction) 1,316 individuals NA Affymetrix, Illumina [279409] (imputed) 766 neurofibrillary tangles measurement http://www.ebi.ac.uk/efo/EFO_0006797 GCST010343 Genome-wide genotyping array 2021-06-04 32970232 Zhang YX 2020-09-24 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/32970232 Three pleiotropic loci associated with bone mineral density and lean body mass. Bone mineral density or leg lean mass (pleiotropy) 9,618 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals up to 500,000 European ancestry individuals Affymetrix, Illumina [12061510] (imputed) 2 bone density, lean body mass http://www.ebi.ac.uk/efo/EFO_0003923, http://www.ebi.ac.uk/efo/EFO_0004995 GCST011788 Genome-wide genotyping array 2021-06-04 32970232 Zhang YX 2020-09-24 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/32970232 Three pleiotropic loci associated with bone mineral density and lean body mass. Bone mineral density 9,618 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals up to 500,000 European ancestry individuals Affymetrix, Illumina [12061510] (imputed) 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST011789 Genome-wide genotyping array 2021-06-04 32970232 Zhang YX 2020-09-24 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/32970232 Three pleiotropic loci associated with bone mineral density and lean body mass. Arm lean mass 9,618 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals up to 500,000 European ancestry individuals Affymetrix, Illumina [12061510] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST011790 Genome-wide genotyping array 2021-06-04 32970232 Zhang YX 2020-09-24 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/32970232 Three pleiotropic loci associated with bone mineral density and lean body mass. Leg lean mass 9,618 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals up to 500,000 European ancestry individuals Affymetrix, Illumina [12061510] (imputed) 2 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST011792 Genome-wide genotyping array 2021-06-04 32970232 Zhang YX 2020-09-24 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/32970232 Three pleiotropic loci associated with bone mineral density and lean body mass. Bone mineral density or leg lean mass (pleiotropy) 9,618 European ancestry individuals, 1,539 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals up to 500,000 European ancestry individuals Affymetrix, Illumina [12061510] (imputed) 0 bone density, lean body mass http://www.ebi.ac.uk/efo/EFO_0003923, http://www.ebi.ac.uk/efo/EFO_0004995 GCST011791 Genome-wide genotyping array 2021-03-29 32758111 He M 2020-08-06 J Dent Res www.ncbi.nlm.nih.gov/pubmed/32758111 Genome-wide Analyses Identify a Novel Risk Locus for Nonsyndromic Cleft Palate. Nonsyndromic cleft palate 994 Han Chinese ancestry cases, 2,963 Han Chinese ancestry controls 1,095 Han Chinese ancestry cases, 6,352 Han Chinese ancestry controls Illumina [750091] 5 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST011425 Genome-wide genotyping array 2019-01-25 30202859 Laisk T 2018-09-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30202859 Large scale meta-analysis highlights the hypothalamic-pituitary-gonadal (HPG) axis in the genetic regulation of menstrual cycle length. Length of menstrual cycle 44,871 European ancestry women NA Illumina [9344826] (imputed) 5 menstrual cycle measurement http://www.ebi.ac.uk/efo/EFO_0007786 GCST006958 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Human herpes virus 7 U14 antibody levels 8,528 White British ancestry individuals NA NR [25472218] (imputed) 3 anti-human herpes virus 7 antibody measurement http://www.ebi.ac.uk/efo/EFO_0011038 GCST90006909 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-helicobacter pylori IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 Helicobacter pylori seropositivity http://www.ebi.ac.uk/efo/EFO_0009341 GCST90006910 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Helicobacter pylori CagA antibody levels 985 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-Helicobacter pylori IgG measurement http://www.ebi.ac.uk/efo/EFO_0009352 GCST90006911 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Helicobacter pylori Catalase antibody levels 1,558 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-Helicobacter pylori IgG measurement http://www.ebi.ac.uk/efo/EFO_0009352 GCST90006912 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Helicobacter pylori GroEL antibody levels 2,716 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-Helicobacter pylori IgG measurement http://www.ebi.ac.uk/efo/EFO_0009352 GCST90006913 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Helicobacter pylori OMP antibody levels 2,640 White British ancestry individuals NA NR [25472218] (imputed) 1 Anti-Helicobacter pylori IgG measurement http://www.ebi.ac.uk/efo/EFO_0009352 GCST90006914 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Helicobacter pylori UREA antibody levels 2,251 White British ancestry individuals NA NR [25472218] (imputed) 1 Anti-Helicobacter pylori IgG measurement http://www.ebi.ac.uk/efo/EFO_0009352 GCST90006915 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Helicobacter pylori VacA antibody levels 1,571 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-Helicobacter pylori IgG measurement http://www.ebi.ac.uk/efo/EFO_0009352 GCST90006916 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-herpes simplex virus 1 IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 herpes virus seropositivity http://www.ebi.ac.uk/efo/EFO_0007036 GCST90006917 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Herpes simplex virus 1 mgG-1 antibody levels 6,199 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-herpes simplex virus 1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0009349 GCST90006918 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-herpes simplex virus 2 IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 2 Herpes simplex virus 2 seropositivity http://www.ebi.ac.uk/efo/EFO_0009339 GCST90006919 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Herpes simplex virus 2 mgG-1 antibody levels 1,382 White British ancestry individuals NA NR [25472218] (imputed) 3 Anti-herpes simplex virus 2 IgG measurement http://www.ebi.ac.uk/efo/EFO_0009350 GCST90006920 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-polyomavirus 2 IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 2 polyomavirus 2 seropositivity http://www.ebi.ac.uk/efo/EFO_0010907 GCST90006921 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Polyomavirus 2 JC VP1 antibody levels 5,118 White British ancestry individuals NA NR [25472218] (imputed) 2 anti-polyomavirus 2 antibody measurement http://www.ebi.ac.uk/efo/EFO_0010900 GCST90006922 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-Merkel cell polyomavirus IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 2 merkel cell virus seropositivity http://www.ebi.ac.uk/efo/EFO_0010906 GCST90006923 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Merkel cell polyomavirus VP1 antibody levels 5,915 White British ancestry individuals NA NR [25472218] (imputed) 5 anti-merkel cell virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0010899 GCST90006924 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-Toxoplasma gondii IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 Toxoplasma gondii seropositivity http://www.ebi.ac.uk/efo/EFO_0007047 GCST90006925 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Toxoplasma gondii p22 antibody levels 1,308 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-Toxoplasma gondii IgG measurement http://www.ebi.ac.uk/efo/EFO_0009353 GCST90006926 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Toxoplasma gondii sag1 antibody levels 3,919 White British ancestry individuals NA NR [25472218] (imputed) 3 Anti-Toxoplasma gondii IgG measurement http://www.ebi.ac.uk/efo/EFO_0009353 GCST90006927 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-varicella zoster virus IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 1 Varicella zoster virus seropositivity http://www.ebi.ac.uk/efo/EFO_0009340 GCST90006928 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Varicella zoster virus glycoproteins E and I antibody levels 7,595 White British ancestry individuals NA NR [25472218] (imputed) 5 Anti-varicella zoster virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009351 GCST90006929 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-BK polyomavirus IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 BK polyomavirus seropositivity http://www.ebi.ac.uk/efo/EFO_0010905 GCST90006884 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. BK polyomavirus VP1 antibody levels 8,555 White British ancestry individuals NA NR [25472218] (imputed) 1 anti-BK polyomavirus antibody measurement http://www.ebi.ac.uk/efo/EFO_0010904 GCST90006885 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-chlamydia trachomatis IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 1 Chlamydia trachomatis seropositivity http://www.ebi.ac.uk/efo/EFO_0009330 GCST90006886 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Chlamydia trachomatis momp A antibody levels 964 White British ancestry individuals NA NR [25472218] (imputed) 0 anti-chlamydia trachomatis antibody measurement http://www.ebi.ac.uk/efo/EFO_0010903 GCST90006887 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Chlamydia trachomatis momp D antibody levels 1,371 White British ancestry individuals NA NR [25472218] (imputed) 0 anti-chlamydia trachomatis antibody measurement http://www.ebi.ac.uk/efo/EFO_0010903 GCST90006888 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Chlamydia trachomatis pGP3 antibody levels 1,784 White British ancestry individuals NA NR [25472218] (imputed) 1 anti-chlamydia trachomatis antibody measurement http://www.ebi.ac.uk/efo/EFO_0010903 GCST90006889 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Chlamydia trachomatis PorB antibody levels 273 White British ancestry individuals NA NR [25472218] (imputed) 5 anti-chlamydia trachomatis antibody measurement http://www.ebi.ac.uk/efo/EFO_0010903 GCST90006890 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Chlamydia trachomatis tarp-D F1 antibody levels 1,635 White British ancestry individuals NA NR [25472218] (imputed) 0 anti-chlamydia trachomatis antibody measurement http://www.ebi.ac.uk/efo/EFO_0010903 GCST90006891 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Chlamydia trachomatis tarp-D F2 antibody levels 2,074 White British ancestry individuals NA NR [25472218] (imputed) 0 anti-chlamydia trachomatis antibody measurement http://www.ebi.ac.uk/efo/EFO_0010903 GCST90006892 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-cytomegalovirus IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 cytomegalovirus seropositivity http://www.ebi.ac.uk/efo/EFO_0007037 GCST90006893 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Cytomegalovirus pp28 antibody levels 5,087 White British ancestry individuals NA NR [25472218] (imputed) 1 Anti-cytomegalovirus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009347 GCST90006894 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Cytomegalovirus pp52 antibody levels 5,681 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-cytomegalovirus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009347 GCST90006895 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Cytomegalovirus pp150 antibody levels 5,136 White British ancestry individuals NA NR [25472218] (imputed) 0 Anti-cytomegalovirus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009347 GCST90006896 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-Epstein-Barr virus IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 1 Epstein-Barr virus seropositivity http://www.ebi.ac.uk/efo/EFO_0010908 GCST90006897 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Epstein-Barr virus EA-D antibody levels 7,763 White British ancestry individuals NA NR [25472218] (imputed) 3 anti-Epstein Barr virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0009273 GCST90006898 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Epstein-Barr virus EBNA-1 antibody levels 7,972 White British ancestry individuals NA NR [25472218] (imputed) 2 anti-Epstein Barr virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0009273 GCST90006899 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Epstein-Barr virus VCA p18 antibody levels 8,518 White British ancestry individuals NA NR [25472218] (imputed) 2 anti-Epstein Barr virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0009273 GCST90006900 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Epstein-Barr virus ZEBRA antibody levels 8,191 White British ancestry individuals NA NR [25472218] (imputed) 2 anti-Epstein Barr virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0009273 GCST90006901 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-human herpes virus 6 IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90006902 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-human herpes virus 6 IE1A IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 2 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90006903 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Human herpes virus 6 IE1A antibody levels 6,968 White British ancestry individuals NA NR [25472218] (imputed) 1 anti-human herpes virus 6 antibody measurement http://www.ebi.ac.uk/efo/EFO_0011037 GCST90006904 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-human herpes virus 6 IE1B IgG seropositivity 8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90006905 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Human herpes virus 6 IE1B antibody levels 7,119 White British ancestry individuals NA NR [25472218] (imputed) 0 anti-human herpes virus 6 antibody measurement http://www.ebi.ac.uk/efo/EFO_0011037 GCST90006906 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Human herpes virus 6 p101k antibody levels 1,951 White British ancestry individuals NA NR [25472218] (imputed) 0 anti-human herpes virus 6 antibody measurement http://www.ebi.ac.uk/efo/EFO_0011037 GCST90006907 Genome-wide genotyping array 2020-12-04 33204752 Butler-Laporte G 2020-09-24 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33204752 Genetic Determinants of Antibody-Mediated Immune Responses to Infectious Diseases Agents: A Genome-Wide and HLA Association Study. Anti-human herpes virus 7 IgG seropositivity  8,735 White British ancestry individuals NA NR [25472218] (imputed) 0 human herpesvirus 7 seropositivity http://www.ebi.ac.uk/efo/EFO_0600006 GCST90006908 Genome-wide genotyping array 2019-08-27 31189108 O'Connor D 2019-06-01 Cell Rep www.ncbi.nlm.nih.gov/pubmed/31189108 Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization. Meningococcal C IgG concentrations post childhood immunization 1,203 European ancestry children and adolescents 980 European ancestry children and adolescents Illumina [~ 6700000] (imputed) 1 anti-meningococcal C IgG measurement, response to vaccine http://www.ebi.ac.uk/efo/EFO_0010084, http://www.ebi.ac.uk/efo/EFO_0004645 GCST008498 Genome-wide genotyping array 2019-08-27 31189108 O'Connor D 2019-06-01 Cell Rep www.ncbi.nlm.nih.gov/pubmed/31189108 Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization. Meningococcal C functional antibody titers post childhood immunization 1,585 European ancestry children and adolescents 779 European ancestry children and adolescents Illumina [~ 6700000] (imputed) 6 anti-meningococcal C serum bactericidal antibody measurement, response to vaccine http://www.ebi.ac.uk/efo/EFO_0010087, http://www.ebi.ac.uk/efo/EFO_0004645 GCST008499 Genome-wide genotyping array 2019-08-27 31189108 O'Connor D 2019-06-01 Cell Rep www.ncbi.nlm.nih.gov/pubmed/31189108 Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization. Tetanus toxoid IgG concentrations post childhood immunization 549 European ancestry children and adolescents 1,303 European ancestry children and adolescents Illumina [~ 6700000] (imputed) 1 anti-tetanus toxoid IgG measurement, response to vaccine http://www.ebi.ac.uk/efo/EFO_0010085, http://www.ebi.ac.uk/efo/EFO_0004645 GCST008500 Genome-wide genotyping array 2019-08-27 31189108 O'Connor D 2019-06-01 Cell Rep www.ncbi.nlm.nih.gov/pubmed/31189108 Common Genetic Variations Associated with the Persistence of Immunity following Childhood Immunization. Haemophilus influenza type b polyribosylribitol phosphate IgG concentrations post childhood immunization 967 European ancestry children and adolescents 1,011 European ancestry children and adolescents Illumina [~ 6700000] (imputed) 0 response to vaccine, anti-Haemophilus influenzae type b polyribosylribitol phosphate IgG measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0010086 GCST008501 Genome-wide genotyping array 2022-07-05 35368020 Gong B 2022-04-02 Signal Transduct Target Ther www.ncbi.nlm.nih.gov/pubmed/35368020 A genetic variant in IL-6 lowering its expression is protective for critical patients with COVID-19. COVID-19 (critical illness vs population) 437 Chinese ancestry cases, 2,551 Chinese ancestry controls 195 Chinese ancestry cases, 470 Chinese ancestry controls Illumina [761993] 7 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90105053 Genome-wide genotyping array 2020-11-02 32884031 Chuang GT 2020-09-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32884031 Genome-wide association study for circulating fibroblast growth factor 21 and 23. Circulating fibroblast growth factor 21 levels 4,201 Taiwanese ancestry individuals NA Affymetrix [7897704] (imputed) 3 fibroblast growth factor 21 measurement http://www.ebi.ac.uk/efo/EFO_0010783 GCST90010720 Genome-wide genotyping array 2020-11-02 32884031 Chuang GT 2020-09-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32884031 Genome-wide association study for circulating fibroblast growth factor 21 and 23. Circulating fibroblast growth factor 23 levels 4,201 Taiwanese ancestry individuals NA Affymetrix [7897704] (imputed) 3 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90010721 Genome-wide genotyping array 2022-07-13 35331647 Schmidt AW 2022-03-11 Pancreatology www.ncbi.nlm.nih.gov/pubmed/35331647 Colocalization analysis of pancreas eQTLs with risk loci from alcoholic and novel non-alcoholic chronic pancreatitis GWAS suggests potential disease causing mechanisms. Non-alcoholic chronic pancreatitis 584 European ancestry cases, 6,040 European ancestry controls NA NR [NR] (imputed) 5 non-alcoholic pancreatitis http://www.ebi.ac.uk/efo/EFO_0021524 GCST90104595 Genome-wide genotyping array 2019-11-28 31672989 Lopez-Isac E 2019-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31672989 GWAS for systemic sclerosis identifies multiple risk loci and highlights fibrotic and vasculopathy pathways. Systemic sclerosis 9,095 European ancestry cases, 17,584 European ancestry controls NA Illumina [4723365] 23 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST009131 Genome-wide genotyping array 2019-02-27 30713548 Schurz H 2019-01-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/30713548 A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array. Tuberculosis 242 South African admixed female cases, 168 South African admixed male cases, 223 South African admixed female controls, 182 South African admixed male controls NA Illumina [848325] 12 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST007231 Genome-wide genotyping array 2019-02-27 30713548 Schurz H 2019-01-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/30713548 A Sex-Stratified Genome-Wide Association Study of Tuberculosis Using a Multi-Ethnic Genotyping Array. Tuberculosis (SNP x SNP interaction) 242 South African admixed female cases, 168 South African admixed male cases, 223 South African admixed female controls, 182 South African admixed male controls NA Illumina [848325] 18 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST007232 Genome-wide genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Height 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 4 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST011692 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Weight 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 1 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST011690 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Body mass index 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST011689 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Waist circumference 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 1 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST011688 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Systolic blood pressure 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 9 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011687 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Diastolic blood pressure 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 4 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011686 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Fasting plasma glucose 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 4 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST011685 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Glycated hemoglobin levels 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST011682 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Low density lipoprotein cholesterol levels 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST011683 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. High density lipoprotein cholesterol levels 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 8 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST011684 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Total cholesterol levels 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 7 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST011691 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Triglyceride levels 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 14 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011693 Genome-wide genotyping array, Targeted genotyping array 2021-05-18 32902719 Hebbar P 2020-09-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32902719 Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population. Non-HDL cholesterol levels 2,732 Kuwaiti ancestry individuals NA Illumina [up to 1520000] (imputed) 7 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST011694 Genome-wide genotyping array, Targeted genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Body mass index 17,127 African American individuals, 21,955 Hispanic/Latino individuals, 4,647 Asian ancestry individuals, 3,936 Native Hawaiian ancestry individuals, 645 Native American ancestry individuals, 1,025 individuals NA Illumina [32062178] (imputed) 63 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008025 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Chronic kidney disease 1,533 African American cases, 1,339 Hispanic/Latino cases, 575 Asian ancestry cases, 608 Native Hawaiian ancestry cases, 42 Native American ancestry cases, 57 cases, 13,989 African American controls, 19,581 Hispanic/Latino controls, 3,549 Asian ancestry controls, 2,892 Native Hawaiian ancestry controls, 597 Native American ancestry controls, 965 controls NA Illumina [17780322] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST008026 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Smoking behaviour (cigarettes smoked per day) 7,171 African American individuals, 4,198 Hispanic/Latino individuals, 1,918 Asian ancestry individuals, 2,176 Native Hawaiian ancestry individuals, 288 Native American ancestry individuals, 111 individuals NA Illumina [27957689] (imputed) 5 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST008027 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Coffee consumption (cups per day) 11,862 African American individuals, 15,837 Hispanic/Latino individuals, 3,764 Asian ancestry individuals, 3,857 Native Hawaiian ancestry individuals, 582 Native American ancestry individuals NA Illumina [32504442] (imputed) 16 cups of coffee per day measurement http://www.ebi.ac.uk/efo/EFO_0006782 GCST008028 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Diastolic blood pressure 11,380 African American individuals, 21,549 Hispanic/Latino individuals, 1,086 Asian ancestry individuals, 636 Native American ancestry individuals, 782 individuals NA Illumina [32101933] (imputed) 13 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST008029 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Estimated glomerular filtration rate 8,261 African American individuals, 18,548 Hispanic/Latino individuals, 150 Asian ancestry individuals, 602 Native American ancestry individuals, 339 individuals NA Illumina [30341014] (imputed) 9 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST008030 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. End-stage renal disease 326 African American cases, 208 Hispanic/Latino cases, 24 Asian ancestry cases, 21 Native Hawaiian ancestry cases, 1 Native American ancestry case, 22 cases, 8,739 African American controls, 16,197 Hispanic/Latino controls, 3,576 Asian ancestry controls, 2,925 Native Hawaiian ancestry controls, 52 Native American ancestry controls, 970 controls NA Illumina [11665604] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST008031 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Fasting blood glucose 6,457 African American individuals, 13,556 Hispanic/Latino individuals, 1,918 Asian ancestry individuals, 1,400 Native Hawaiian ancestry individuals, 412 Native American ancestry individuals, 168 individuals NA Illumina [29713514] (imputed) 28 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST008032 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Fasting blood insulin 5,525 African American individuals, 12,687 Hispanic/Latino individuals, 1,547 Asian ancestry individuals, 1,397 Native Hawaiian ancestry individuals, 395 Native American ancestry individuals NA Illumina [28840767] (imputed) 6 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST008033 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Hemoglobin A1c levels 559 African American individuals, 10,408 Hispanic/Latino individuals, 92 Asian ancestry individuals, 4 Native American ancestry individuals, 115 individuals NA Illumina [22871999] (imputed) 20 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST008034 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. High density lipoprotein cholesterol levels 10,085 African American individuals, 17,751 Hispanic/Latino individuals, 2,378 Asian ancestry individuals, 1,912 Native Hawaiian ancestry individuals, 604 Native American ancestry individuals, 333 individuals NA Illumina [31978362] (imputed) 153 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008035 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Hypertension 11,863 African American cases, 8,663 Hispanic/Latino cases, 3,102 Asian ancestry cases, 2,645 Native Hawaiian ancestry cases, 342 Native American ancestry cases, 508 cases, 5,289 African American controls, 13,273 Hispanic/Latino controls, 1,561 Asian ancestry controls, 1,060 Native Hawaiian ancestry controls, 293 Native American ancestry controls, 542 controls NA Illumina [28263875] (imputed) 2 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST008036 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Low density lipoprotein cholesterol levels 9,720 African American individuals, 17,373 Hispanic/Latino individuals, 2,316 Asian ancestry individuals, 1,900 Native Hawaiian ancestry individuals, 591 Native American ancestry individuals, 321 individuals NA Illumina [31808917] (imputed) 131 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008037 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Mean corpuscular hemoglobin concentration 3,750 African American individuals, 15,522 Hispanic/Latino individuals, 128 Asian ancestry individuals, 20 Native American ancestry individuals, 383 individuals NA Illumina [27815891] (imputed) 16 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST008038 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Platelet count 8,850 African American individuals, 18,949 Hispanic/Latino individuals, 541 Asian ancestry individuals, 603 Native American ancestry individuals, 385 individuals NA Illumina [30743395] (imputed) 36 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST008039 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. PR interval 3,360 African American individuals, 13,702 Hispanic/Latino individuals, 129 Asian ancestry individuals, 231 Native American ancestry individuals NA Illumina [26703325] (imputed) 31 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST008042 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. QT interval 3,293 African American individuals, 13,698 Hispanic/Latino individuals, 127 Asian ancestry individuals, 230 Native American ancestry individuals NA Illumina [26659972] (imputed) 51 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST008043 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Systolic blood pressure 11,380 African American individuals, 21,549 Hispanic/Latino individuals, 1,086 Asian ancestry individuals, 636 Native American ancestry individuals, 782 individuals NA Illumina [32101933] (imputed) 13 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST008044 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Total cholesterol levels 10,137 African American individuals, 17,802 Hispanic/Latino individuals, 2,387 Asian ancestry individuals, 1,915 Native Hawaiian ancestry individuals, 604 Native American ancestry individuals, 340 individuals NA Illumina [32003504] (imputed) 170 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST008045 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Triglyceride levels 9,980 African American individuals, 17,856 Hispanic/Latino individuals, 2,381 Asian ancestry individuals, 1,915 Native Hawaiian ancestry individuals, 604 Native American ancestry individuals, 360 individuals NA Illumina [31978265] (imputed) 137 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST008046 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Type 2 diabetes 5,971 African American cases, 4,135 Hispanic/Latino cases, 2,004 Asian ancestry cases, 1,534 Native Hawaiian ancestry cases, 167 Native American ancestry cases, 231 cases, 9,630 African American controls, 16,345 Hispanic/Latino controls, 2,572 Asian ancestry controls, 2,017 Native Hawaiian ancestry controls, 452 Native American ancestry controls, 667 controls NA Illumina [24011241] (imputed) 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST008048 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. White blood cell count 8,825 African American individuals, 18,251 Hispanic/Latino individuals, 543 Asian ancestry individuals, 606 Native American ancestry individuals, 383 individuals NA Illumina [30613845] (imputed) 47 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST008049 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Waist-hip ratio 9,140 African American females, 11,555 Hispanic/Latino females, 1,843 Asian ancestry females, 1,715 Native Hawaiian ancestry females, 585 Native American ancestry females NA Illumina [30305130] (imputed) 12 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008050 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Waist-hip ratio 1,146 African American males, 4,917 Hispanic/Latino males, 1,657 Asian ancestry males, 1,346 Native Hawaiian ancestry males NA Illumina [21894105] (imputed) 2 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008051 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Waist-hip ratio 10,286 African American individuals, 16,472 Hispanic/Latino individuals, 3,500 Asian ancestry individuals, 3,061 Native Hawaiian ancestry individuals, 585 Native American ancestry individuals NA Illumina [at least 21894105] (imputed) 11 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST008052 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Breast cancer 17,881 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 77 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90011804 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Testicular cancer 713 European ancestry cases, 359,825 European ancestry controls NA Affymetrix [7846216] (imputed) 16 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST90011805 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Oral cavity and pharyngeal cancer 1,223 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 10 oropharynx cancer http://www.ebi.ac.uk/efo/EFO_1001931 GCST90011806 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Esophageal or stomach cancer 1,091 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 11 esophageal carcinoma, gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0002916, http://www.ebi.ac.uk/efo/EFO_0000178 GCST90011807 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Prostate cancer 10,792 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 65 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90011808 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Melanoma 6,777 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 38 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90011809 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Rectal cancer 2,091 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 12 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90011810 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Colon cancer 3,793 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 13 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90011811 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Lung cancer 2,485 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 8 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90011812 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Thyroid cancer 762 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 14 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90011813 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Lymphocytic leukemia 852 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 24 lymphoid leukemia http://www.ebi.ac.uk/efo/EFO_0004289 GCST90011814 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Pancreatic cancer 663 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 12 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90011815 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Cervical cancer 6,563 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 11 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90011816 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Bladder cancer 2,242 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 10 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90011817 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Kidney cancer 1,338 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 10 kidney cancer http://purl.obolibrary.org/obo/MONDO_0002367 GCST90011818 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Non-Hodgkin's lymphoma 2,400 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 15 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90011819 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Endometrial cancer 2,037 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 7 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST90011820 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Ovarian cancer 1,259 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 1 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90011821 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Cancer (pleiotropy) 64,962 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 137 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90011822 Genome-wide genotyping array 2020-11-13 32887889 Rashkin SR 2020-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32887889 Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts. Cancer (pleiotropy)(bidirectional) 64,962 European ancestry cases, 410,350 European ancestry controls NA Affymetrix [7846216] (imputed) 21 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90011823 Genome-wide genotyping array 2019-07-12 23263489 Huyghe JR 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263489 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Fasting blood proinsulin levels up to 8,229 Finnish ancestry non-diabetic individuals NA Illumina [242071] 8 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST008109 Exome genotyping array [Exome array] 2019-07-12 23263489 Huyghe JR 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263489 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Insulinogenic index up to 8,229 Finnish ancestry non-diabetic individuals NA Illumina [242071] 4 Insulinogenic index measurement http://www.ebi.ac.uk/efo/EFO_0009961 GCST008110 Exome genotyping array [Exome array] 2019-07-12 23263489 Huyghe JR 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263489 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Insulin disposition index up to 8,229 Finnish ancestry non-diabetic individuals NA Illumina [242071] 1 disposition index measurement http://www.ebi.ac.uk/efo/EFO_0006832 GCST008111 Exome genotyping array [Exome array] 2019-07-12 23263489 Huyghe JR 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263489 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Proinsulin levels (late-phase conversion) up to 8,229 Finnish ancestry non-diabetic individuals NA Illumina [242071] 1 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST008113 Exome genotyping array [Exome array] 2019-07-12 23263489 Huyghe JR 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263489 Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion. Proinsulin levels (early-phase conversion) up to 8,229 Finnish ancestry non-diabetic individuals NA Illumina [242071] 1 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST008112 Exome genotyping array [Exome array] 2019-02-26 30566020 Fukaya E 2018-12-01 Circulation www.ncbi.nlm.nih.gov/pubmed/30566020 Clinical and Genetic Determinants of Varicose Veins. Varicose veins 9,577 British ancestry cases, 327,959 British ancestry controls NA Affymetrix [10972371] (imputed) 30 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST007225 Genome-wide genotyping array 2019-08-14 31186284 Liu Y 2019-06-11 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/31186284 A genome wide association study on lipoprotein(a) levels and coronary artery disease severity in a Chinese population. Lipoprotein (a) levels in coronary artery disease (percutaneous coronary intervention) 1,402 Han Chinese ancestry individuals NA Illumina [3448668] (imputed) 4 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST008433 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Height 17,286 African American individuals, 22,192 Hispanic/Latino individuals, 4,680 Asian ancestry individuals, 3,939 Native Hawaiian ancestry individuals, 647 Native American ancestry individuals, 1,052 individuals NA Illumina [34656550] (imputed) 214 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST008053 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Height 303,288 European ancestry individuals NA Illumina [~ 2500000] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST008040 Genome-wide genotyping array 2019-07-01 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. Height 253,288 European ancestry individuals, 17,286 African American individuals, 22,192 Hispanic/Latino individuals, 4,680 Asian ancestry individuals, 3,939 Native Hawaiian ancestry individuals, 647 Native American ancestry individuals, 1,052 individuals NA Illumina [~ 2500000] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST008041 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. QRS duration 3,274 African American individuals, 13,420 Hispanic/Latino individuals, 126 Asian ancestry individuals, 226 Native American ancestry individuals NA Illumina [26566045] (imputed) 26 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST008054 Genome-wide genotyping array 2019-07-02 31217584 Wojcik GL 2019-06-19 Nature www.ncbi.nlm.nih.gov/pubmed/31217584 Genetic analyses of diverse populations improves discovery for complex traits. C-reactive protein levels 8,349 African American individuals, 15,912 Hispanic/Latino individuals, 1,811 Asian ancestry individuals, 1,777 Native Hawaiian ancestry individuals, 574 Native American ancestry individuals, 97 individuals NA Illumina [30861016] (imputed) 45 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST008055 Genome-wide genotyping array 2021-06-18 33105104 Hoi-Yee Li G 2020-12-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/33105104 Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis. Thyrotoxic periodic paralysis 319 Chinese ancestry cases, 3,516 Chinese ancestry controls NA Illumina [7077246] (imputed) 4 thyrotoxic periodic paralysis http://purl.obolibrary.org/obo/MONDO_0019201 GCST011933 Genome-wide genotyping array 2021-06-18 33105104 Hoi-Yee Li G 2020-12-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/33105104 Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis. Thyrotoxic periodic paralysis 306 Chinese ancestry male cases, 3,516 Chinese ancestry controls NA Illumina [7076963] (imputed) 51 thyrotoxic periodic paralysis http://purl.obolibrary.org/obo/MONDO_0019201 GCST011932 Genome-wide genotyping array 2022-07-13 35295415 Wang RS 2022-01-04 Front Pain Res (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35295415 Genomic Effects Associated With Response to Placebo Treatment in a Randomized Trial of Irritable Bowel Syndrome. Response to treatment in irritable bowel syndrome (symptom severity) 54 European ancestry double-blind placebo-treated individuals, 53 European ancestry open-label placebo-treated individuals, 62 European ancestry no pill control-treated individuals, 9 double-blind placebo-treated individuals, 10 open-label placebo-treated individuals, 10 no pill control-treated individuals NA Illumina [NR] (imputed) 12 irritable bowel syndrome symptom measurement http://www.ebi.ac.uk/efo/EFO_0021536 GCST90128542 Genome-wide genotyping array 2021-01-27 33125391 Hassler S 2020-10-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/33125391 Clinicogenomic factors of biotherapy immunogenicity in autoimmune disease: A prospective multicohort study of the ABIRISK consortium. Anti-drug antibodies in autoimmune disease (time to event) 457 European ancestry individuals NA Illumina [351824] 5 anti-drug antibody measurement http://www.ebi.ac.uk/efo/EFO_0010559 GCST010993 Genome-wide genotyping array 2021-01-25 33125193 Daghlas I 2020-10-30 Ann Clin Transl Neurol www.ncbi.nlm.nih.gov/pubmed/33125193 Habitual sleep disturbances and migraine: a Mendelian randomization study. Snoring 421,466 European ancestry individuals NA NR [NR] (imputed) 0 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST010982 Genome-wide genotyping array 2021-01-25 33125193 Daghlas I 2020-10-30 Ann Clin Transl Neurol www.ncbi.nlm.nih.gov/pubmed/33125193 Habitual sleep disturbances and migraine: a Mendelian randomization study. Difficulty awakening 451,872 European ancestry individuals NA NR [NR] (imputed) 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST010981 Genome-wide genotyping array 2021-02-05 33115273 Hoekstra M 2020-10-29 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/33115273 Genome-Wide Association Study Highlights APOH as a Novel Locus for Lipoprotein(a) Levels. Lipoprotein (a) levels 293,274 White ancestry individuals 5,465 White ancestry individuals, 6,101 South Asian ancestry individuals, 2,510 Sub-Saharan African ancestry individuals, 3,207 Black Caribbean ancestry individuals Affymetrix [9829003] (imputed) 1 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST011087 Genome-wide genotyping array 2021-02-18 33128006 Timmins IR 2020-10-30 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33128006 Genome-wide association study of self-reported walking pace suggests beneficial effects of brisk walking on health and survival. Walking pace 450,967 European ancestry individuals NA Affymetrix [10061374] (imputed) 75 gait measurement http://www.ebi.ac.uk/efo/EFO_0007680 GCST011122 Genome-wide genotyping array 2019-03-05 30557370 Baas J 2018-12-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/30557370 Genome wide association study to identify predictors for severe skin toxicity in colorectal cancer patients treated with cetuximab. Severe skin toxicity response to cetuximab in colorectal cancer 36 cases, 246 controls with no or mild skin toxicity NA Illumina [5830976] (imputed) 8 skin disease, response to cetuximab http://www.ebi.ac.uk/efo/EFO_0000701, http://www.ebi.ac.uk/efo/EFO_0007682 GCST007259 Genome-wide genotyping array 2021-01-18 33114509 Park J 2020-10-26 J Pers Med www.ncbi.nlm.nih.gov/pubmed/33114509 Association of an APBA3 Missense Variant with Risk of Premature Ovarian Failure in the Korean Female Population. Premature ovarian failure 60 Korean ancestry cases, 182 Korean ancestry controls 105 Korean ancestry cases, 217 Korean ancestry controls Affymetrix [166866] 0 primary ovarian insufficiency http://www.ebi.ac.uk/efo/EFO_0004266 GCST010976 Genome-wide genotyping array 2021-06-24 33114701 Jee D 2020-10-26 Nutrients www.ncbi.nlm.nih.gov/pubmed/33114701 Polygenetic-Risk Scores for A Glaucoma Risk Interact with Blood Pressure, Glucose Control, and Carbohydrate Intake. Glaucoma 377 Korean ancestry cases, 47,820 Korean ancestry controls NA Affymetrix [NR] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST011963 Genome-wide genotyping array 2020-07-20 29343252 Hendry LM 2018-01-17 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/29343252 Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort. Diastolic blood pressure 1,947 African ancestry individuals NA Illumina [125906] 2 diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006945 GCST010216 Targeted genotyping array [Metabochip] 2020-07-20 29343252 Hendry LM 2018-01-17 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/29343252 Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort. Systolic blood pressure 1,947 African ancestry individuals NA Illumina [125906] 1 systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006944 GCST010217 Targeted genotyping array [Metabochip] 2020-09-21 32766472 Park SL 2020-06-25 Hepatol Commun www.ncbi.nlm.nih.gov/pubmed/32766472 Genome-Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study. Nonalcoholic fatty liver disease 37 African American cases, 177 Japanese American cases, 140 Latino cases, 85 Native Hawaiian cases, 67 European ancestry cases, 218 African American controls, 221 Japanese American controls, 182 Latino controls, 158 Native Hawaiian controls, 244 European ancestry controls NA Illumina [9789995] (imputed) 8 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST010597 Genome-wide genotyping array 2020-09-21 32766472 Park SL 2020-06-25 Hepatol Commun www.ncbi.nlm.nih.gov/pubmed/32766472 Genome-Wide Association Study of Liver Fat: The Multiethnic Cohort Adiposity Phenotype Study. Percent liver fat 269 African American individuals, 424 Japanese American individuals, 345 Latino individuals, 270 Native Hawaiian individuals, 382 European ancestry individuals NA Illumina [9789995] (imputed) 5 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST010598 Genome-wide genotyping array 2019-02-13 30153862 Maxwell TJ 2018-08-28 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/30153862 Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels. Cerebrospinal fluid t-tau:AB1-42 ratio 3,146 European ancestry individuals NA Illumina [5088365] (imputed) 5 t-tau:beta-amyloid 1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0007708 GCST007130 Genome-wide genotyping array 2019-02-13 30153862 Maxwell TJ 2018-08-28 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/30153862 Genome-wide association study for variants that modulate relationships between cerebrospinal fluid amyloid-beta 42, tau, and p-tau levels. Cerebrospinal fluid t-tau:AB1-42 ratio 3,146 European ancestry individuals NA Illumina [5088365] (imputed) 3 t-tau:beta-amyloid 1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0007708 GCST007129 Genome-wide genotyping array 2020-12-11 33020668 Koyama S 2020-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33020668 Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease. Coronary artery disease 25,892 Japanese ancestry cases, 142,336 Japanese ancestry controls NA Illumina [19707525] (imputed) 73 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST010867 Genome-wide genotyping array 2020-12-11 33020668 Koyama S 2020-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33020668 Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease. Coronary artery disease 25,892 Japanese ancestry cases, 95,342 European ancestry cases, 142,336 Japanese ancestry controls, 385,488 European ancestry controls NA Illumina [4804024] (imputed) 175 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST010866 Genome-wide genotyping array 2020-08-25 32421744 Gzara C 2020-05-18 PLoS Pathog www.ncbi.nlm.nih.gov/pubmed/32421744 Family-based genome-wide association study of leprosy in Vietnam. Leprosy 1,749 Vietnamese ancestry cases 1,181 Vietnamese ancestry cases, 688 Vietnamese ancestry controls Illumina [5607170] (imputed) 5 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST010457 Genome-wide genotyping array 2021-05-21 32918390 Lin GY 2020-09-12 Ann Clin Transl Neurol www.ncbi.nlm.nih.gov/pubmed/32918390 Association of genetic variants in migraineurs with and without restless legs syndrome. Restless legs syndrome in migraine without aura 27 Taiwanese ancestry cases, 142 Taiwanese ancestry controls NA Affymetrix [710525] 5 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST011712 Genome-wide genotyping array 2021-05-21 32918390 Lin GY 2020-09-12 Ann Clin Transl Neurol www.ncbi.nlm.nih.gov/pubmed/32918390 Association of genetic variants in migraineurs with and without restless legs syndrome. Restless legs syndrome in migraine with aura 26 Taiwanese ancestry cases, 34 Taiwanese ancestry controls NA Affymetrix [710525] 0 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST011711 Genome-wide genotyping array 2021-05-21 32918390 Lin GY 2020-09-12 Ann Clin Transl Neurol www.ncbi.nlm.nih.gov/pubmed/32918390 Association of genetic variants in migraineurs with and without restless legs syndrome. Restless legs syndrome in migraine 53 Taiwanese ancestry cases, 180 Taiwanese ancestry controls NA Affymetrix [710525] 2 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST011710 Genome-wide genotyping array 2020-08-27 32433515 Meyers JL 2020-05-20 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/32433515 A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior. Theta EEG coherence 6,644 European ancestry individuals, 2,166 African American individuals NA Illumina [6832792] (imputed) 4 theta wave measurement http://www.ebi.ac.uk/efo/EFO_0006873 GCST010464 Genome-wide genotyping array 2020-09-07 32433338 St Jean PL 2020-05-19 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/32433338 Pharmacogenetic assessment of tafenoquine efficacy in patients with Plasmodium vivax malaria. Tafenoquine efficacy in P. vivax malaria (recurrence by 6 months) 438 cases NA Affymetrix [10600000] (imputed) 1 disease recurrence, response to tafenoquine http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0010808 GCST010503 Genome-wide genotyping array 2020-09-07 32433338 St Jean PL 2020-05-19 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/32433338 Pharmacogenetic assessment of tafenoquine efficacy in patients with Plasmodium vivax malaria. Tafenoquine efficacy in P. vivax malaria (recurrence by 4 months) 438 cases NA Affymetrix [10600000] (imputed) 1 disease recurrence, response to tafenoquine http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0010808 GCST010502 Genome-wide genotyping array 2020-09-07 32433338 St Jean PL 2020-05-19 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/32433338 Pharmacogenetic assessment of tafenoquine efficacy in patients with Plasmodium vivax malaria. Tafenoquine efficacy in P. vivax malaria (time to recurrence up to 6 months) 438 cases NA Affymetrix [10600000] (imputed) 0 disease recurrence, response to tafenoquine http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0010808 GCST010501 Genome-wide genotyping array 2021-01-27 32428537 Meguro A 2020-05-16 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/32428537 Genome-wide association study in Asians identifies novel loci for high myopia and highlights a nervous system role in its pathogenesis. High myopia 1,632 Japanese ancestry cases, 1,586 Japanese ancestry controls 800 East Asian ancestry cases, 81 Singaporean ancestry cases, 5,169 East Asian ancestry controls, 4,777 Singaporean ancestry controls Affymetrix, Illumina [4996193] (imputed) 9 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST010994 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Major depressive disorder (lifetime) 16,301 British ancestry cases, 50,870 British ancestry controls NA NR [5276842] (imputed) 4 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010009 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Major depressive disorder (lifetime with recurrence) 10,302 British ancestry cases, 49,083 British ancestry controls NA NR [5276842] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010010 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Help-seeking from a GP 113,262 British ancestry cases, 219,360 British ancestry controls NA NR [5276842] (imputed) 28 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010011 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Help-seeking from a psychiatrist 36,286 British ancestry cases, 297,126 British ancestry controls NA NR [5276842] (imputed) 5 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010012 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Major depressive disorder symptoms (low mood or anhedonia) 21,177 British ancestry cases, 58,398 British ancestry controls NA NR [5276842] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010013 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Help-seeking from a GP (without major depressive disorder symptoms) 8,632 British ancestry cases, 49,493 British ancestry controls NA NR [5276842] (imputed) 3 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010014 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Depression or depression symptoms 19,805 British ancestry cases, 234,114 British ancestry controls NA NR [5276842] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010015 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Depression 9,176 British ancestry cases, 203,235 British ancestry controls NA NR [5276842] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST010016 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Neuroticism 274,107 British ancestry individuals NA NR [8968716] (imputed) 64 neurotic disorder http://www.ebi.ac.uk/efo/EFO_0004257 GCST010017 Genome-wide genotyping array 2020-05-29 32231276 Cai N 2020-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32231276 Minimal phenotyping yields genome-wide association signals of low specificity for major depression. Smoking status (ever vs never smokers) 336,066 British ancestry individuals NA NR [8968716] (imputed) 36 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST010018 Genome-wide genotyping array 2021-03-19 32755526 D'Urso S 2020-08-05 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/32755526 Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis. Septic shock (28-day mortality) 90 European ancestry cases, 403 European ancestry controls NA Illumina [7590211] (imputed) 1 septic shock http://www.ebi.ac.uk/efo/EFO_0006834 GCST011301 Genome-wide genotyping array 2021-03-19 32755526 D'Urso S 2020-08-05 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/32755526 Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis. Septic shock (90-day mortality) 112 European ancestry cases, 381 European ancestry controls NA Illumina [7590211] (imputed) 0 septic shock http://www.ebi.ac.uk/efo/EFO_0006834 GCST011302 Genome-wide genotyping array 2021-03-19 32755526 D'Urso S 2020-08-05 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/32755526 Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis. Septic shock resolution 459 European ancestry cases, 34 European ancestry controls NA Illumina [7590211] (imputed) 3 septic shock http://www.ebi.ac.uk/efo/EFO_0006834 GCST011304 Genome-wide genotyping array 2021-03-19 32755526 D'Urso S 2020-08-05 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/32755526 Septic Shock: A Genomewide Association Study and Polygenic Risk Score Analysis. Septic shock 493 European ancestry cases, 2,442 European ancestry controls NA Illumina [7567032] (imputed) 1 septic shock http://www.ebi.ac.uk/efo/EFO_0006834 GCST011303 Genome-wide genotyping array 2020-11-12 32805626 Yuan S 2020-08-14 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/32805626 Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study. Tumor necrosis factor levels 30,912 European ancestry individuals NA NR [NR] 4 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST010738 Genome-wide genotyping array 2020-09-10 32747698 Matoba N 2020-08-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32747698 Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. Autism spectrum disorder 22,916 European ancestry cases, 37 African ancestry cases, 83 East Asian ancestry cases, 1,567 cases, 32,504 European ancestry controls, 37 African ancestry controls, 83 East Asian ancestry controls, 1,567 controls NA Illumina [up to 8992756] (imputed) 0 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST010513 Genome-wide genotyping array 2020-09-10 32747698 Matoba N 2020-08-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32747698 Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. Autism spectrum disorder 4,535 European ancestry cases, 37 African ancestry cases, 83 East Asian ancestry cases, 1,567 cases, 4,535 European ancestry controls, 37 African ancestry controls, 83 East Asian ancestry controls, 1,567 controls NA Illumina [8992756] (imputed) 17 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST010515 Genome-wide genotyping array 2020-09-10 32747698 Matoba N 2020-08-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32747698 Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism. Autism spectrum disorder 22,916 European ancestry cases, 32,504 European ancestry controls NA Illumina [up to 8992756] (imputed) 5 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST010514 Genome-wide genotyping array 2021-03-24 32723796 Mehta SD 2020-07-28 mSystems www.ncbi.nlm.nih.gov/pubmed/32723796 Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women. Vaginal microbiome composition (L. iners) 171 Kenyan ancestry individuals NA Illumina [336151] (imputed) 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST011387 Genome-wide genotyping array 2021-03-24 32723796 Mehta SD 2020-07-28 mSystems www.ncbi.nlm.nih.gov/pubmed/32723796 Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women. Vaginal microbiome composition (G. vaginalis) 171 Kenyan ancestry individuals NA Illumina [336151] (imputed) 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST011386 Genome-wide genotyping array 2021-03-24 32723796 Mehta SD 2020-07-28 mSystems www.ncbi.nlm.nih.gov/pubmed/32723796 Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women. Vaginal microbiome composition (Shannon diversity index) 171 Kenyan ancestry individuals NA Illumina [336151] (imputed) 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST011385 Genome-wide genotyping array 2021-03-24 32723796 Mehta SD 2020-07-28 mSystems www.ncbi.nlm.nih.gov/pubmed/32723796 Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women. Vaginal microbiome composition (community state type) 171 Kenyan ancestry individuals NA Illumina [336151] (imputed) 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST011384 Genome-wide genotyping array 2021-03-24 32723796 Mehta SD 2020-07-28 mSystems www.ncbi.nlm.nih.gov/pubmed/32723796 Host Genetic Factors Associated with Vaginal Microbiome Composition in Kenyan Women. Vaginal microbiome composition (L. crispatus) 42 Kenyan ancestry cases, 129 Kenyan ancestry controls NA Illumina [336151] (imputed) 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST011388 Genome-wide genotyping array 2020-07-23 32499652 Asgari S 2020-05-13 Nature www.ncbi.nlm.nih.gov/pubmed/32499652 A positively selected FBN1 missense variant reduces height in Peruvian individuals. Height 598 Peruvian individuals NA Illumina [NR] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST010311 Genome-wide genotyping array 2020-07-23 32499652 Asgari S 2020-05-13 Nature www.ncbi.nlm.nih.gov/pubmed/32499652 A positively selected FBN1 missense variant reduces height in Peruvian individuals. Height 3,134 Peruvian individuals 598 Peruvian individuals Affymetrix [7756401] (imputed) 1 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90002224 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 1) 18,096 European individuals Affymetrix [14134301] (imputed) 0 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000287 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 2) 18,096 European individuals Affymetrix [14134301] (imputed) 5 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000288 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 3) 18,096 European individuals Affymetrix [14134301] (imputed) 8 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000289 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 4) 18,096 European individuals Affymetrix [14134301] (imputed) 9 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000290 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 5) 18,096 European individuals Affymetrix [14134301] (imputed) 9 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000291 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 6) 18,096 European individuals Affymetrix [14134301] (imputed) 11 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000292 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 7) 18,096 European individuals Affymetrix [14134301] (imputed) 8 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000293 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 8) 18,096 European individuals Affymetrix [14134301] (imputed) 6 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000294 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slice 9) 18,096 European individuals Affymetrix [14134301] (imputed) 2 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000295 Genome-wide genotyping array 2020-09-07 32814899 Meyer HV 2020-08-19 Nature www.ncbi.nlm.nih.gov/pubmed/32814899 Genetic and functional insights into the fractal structure of the heart. Myocardial fractal dimension (slices 1-9) 18,096 European individuals NA Affymetrix [14134301] (imputed) 0 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90000296 Genome-wide genotyping array 2021-03-30 32811377 Dueker ND 2020-08-19 Stroke www.ncbi.nlm.nih.gov/pubmed/32811377 Extreme Phenotype Approach Suggests Taste Transduction Pathway for Carotid Plaque in a Multi-Ethnic Cohort. Total carotid plaque area (excess vs minimal atherosclerosis) 180 Hispanic individuals, 100 Black individuals, 60 European ancestry individuals NA Affymetrix [NR] (imputed) 3 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST011436 Genome-wide genotyping array 2021-03-24 32844198 Dumitrescu L 2020-08-01 Brain www.ncbi.nlm.nih.gov/pubmed/32844198 Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Combined resilience (covariance of educational attainment with residual cognitive resilience) 5,108 European ancestry individuals (unimpaired cognition, mild cognitive impairment or Alzheimer’s disease) NA Affymetrix, Illumina [4840740] (imputed) 7 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST011405 Genome-wide genotyping array 2021-03-24 32844198 Dumitrescu L 2020-08-01 Brain www.ncbi.nlm.nih.gov/pubmed/32844198 Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Residual cognitive resilience 5,108 European ancestry individuals (unimpaired cognition, mild cognitive impairment or Alzheimer’s disease) NA Affymetrix, Illumina [4840740] (imputed) 9 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST011406 Genome-wide genotyping array 2021-03-24 32844198 Dumitrescu L 2020-08-01 Brain www.ncbi.nlm.nih.gov/pubmed/32844198 Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Residual cognitive resilience 3,820 European ancestry cognitively unimpaired individuals NA Affymetrix, Illumina [4840740] (imputed) 8 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST011404 Genome-wide genotyping array 2021-03-24 32844198 Dumitrescu L 2020-08-01 Brain www.ncbi.nlm.nih.gov/pubmed/32844198 Genetic variants and functional pathways associated with resilience to Alzheimer's disease. Combined resilience (covariance of educational attainment with residual cognitive resilience) 3,820 European ancestry cognitively unimpaired individuals NA Affymetrix, Illumina [4840740] (imputed) 14 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST011403 Genome-wide genotyping array 2020-10-16 32986714 Fiorica PN 2020-09-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/32986714 Multi-ethnic transcriptome-wide association study of prostate cancer. Prostate cancer 2,463 African American or Afro-Caribbean cases, 2,306 African American or Afro-Caribbean controls NA Illumina [15394464] (imputed) 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90002423 Genome-wide genotyping array 2020-10-16 32986714 Fiorica PN 2020-09-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/32986714 Multi-ethnic transcriptome-wide association study of prostate cancer. Prostate cancer 1,106 Japanese American cases, 1,093 Japanese American controls NA Illumina [4623264] (imputed) 4 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90002424 Genome-wide genotyping array 2020-10-16 32986714 Fiorica PN 2020-09-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/32986714 Multi-ethnic transcriptome-wide association study of prostate cancer. Prostate cancer 1,081 Hispanic or Latin American cases, 1,066 Hispanic or Latin American controls NA Illumina [7010834] (imputed) 1 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90002425 Genome-wide genotyping array 2020-12-10 32938779 Kim HR 2020-09-16 Neurology www.ncbi.nlm.nih.gov/pubmed/32938779 Genetic variants beyond amyloid and tau associated with cognitive decline: A cohort study. Cognitive decline 185 MCI cases, 135 AD cases, 94 controls 39 MCI cases, 11 AC cases, 22 controls Illumina [6221501] (imputed) 0 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST010865 Genome-wide genotyping array 2021-07-07 33002292 Shinohara T 2020-10-01 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/33002292 Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. Glucocorticoid receptor gene expression in B-cell precursor acute lymphoblastic leukaemia 72 Japanese ancestry leukaemic cell lines NA Illumina [331281] 16 glucocorticoid receptor gene expression measurement http://www.ebi.ac.uk/efo/EFO_0600079 GCST011998 Genome-wide genotyping array 2021-07-07 33002292 Shinohara T 2020-10-01 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/33002292 Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. prednisolone sensitivity in B-cell precursor acute lymphoblastic leukaemia 72 Japanese ancestry leukaemic cell lines NA Illumina [331281] 3 response to prednisolone http://www.ebi.ac.uk/efo/EFO_0009168 GCST011997 Genome-wide genotyping array 2021-07-07 33002292 Shinohara T 2020-10-01 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/33002292 Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. dexamethasone sensitivity in B-cell precursor acute lymphoblastic leukaemia 72 Japanese ancestry leukaemic cell lines NA Illumina [331281] 3 response to dexamethasone http://www.ebi.ac.uk/efo/EFO_0010933 GCST011996 Genome-wide genotyping array 2021-07-28 33004991 Sutoh Y 2020-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33004991 ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide G × E interaction analysis. Aspartate aminotransferase levels x alcohol consumption interaction 7,856 Japanese ancestry individuals up to 4,388 Japanese ancestry individuals Illumina [7129678] (imputed) 0 aspartate aminotransferase measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004736, http://www.ebi.ac.uk/efo/EFO_0007878 GCST012144 Genome-wide genotyping array 2021-07-28 33004991 Sutoh Y 2020-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33004991 ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide G × E interaction analysis. Gamma glutamyl transferase levels x alcohol consumption interaction 7,856 Japanese ancestry individuals up to 4,388 Japanese ancestry individuals Illumina [7129678] (imputed) 0 serum gamma-glutamyl transferase measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004532, http://www.ebi.ac.uk/efo/EFO_0007878 GCST012143 Genome-wide genotyping array 2021-07-28 33004991 Sutoh Y 2020-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33004991 ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide G × E interaction analysis. Alanine aminotransferase levels x alcohol consumption interaction 7,856 Japanese ancestry individuals up to 4,388 Japanese ancestry individuals Illumina [7129678] (imputed) 0 serum alanine aminotransferase measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0007878 GCST012142 Genome-wide genotyping array 2021-07-28 33004991 Sutoh Y 2020-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33004991 ALDH2 genotype modulates the association between alcohol consumption and AST/ALT ratio among middle-aged Japanese men: a genome-wide G × E interaction analysis. Aspartate aminotransferase to alanine aminotransferase ratio x alcohol consumption interaction 7,856 Japanese ancestry individuals up to 4,388 Japanese ancestry individuals Illumina [7129678] (imputed) 1 alcohol consumption measurement, aspartate aminotransferase to alanine aminotransferase ratio http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0010934 GCST012141 Genome-wide genotyping array 2020-10-14 32690583 Cheng B 2020-07-20 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/32690583 Genome-Wide Association Analysis Identified ANXA1 Associated with Shoulder Impingement Syndrome in UK Biobank Samples. Shoulder impingement syndrome 7,252 European ancestry individuals NA Affymetrix [825927] (imputed) 20 shoulder impingement syndrome http://www.ebi.ac.uk/efo/EFO_1001178 GCST90010423 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration 10,798 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 3 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011583 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration in non-obese individuals 7,179 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011582 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration in obesity 3,000 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 2 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011581 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration in inactive individuals 5,958 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011580 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration in low fat diet 2,306 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011579 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration in high fat diet 7,873 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 2 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011578 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration in visceral obesity (waist-hip ratio) 2,928 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011577 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum C-reactive protein concentration in visceral obesity (waist circumference) 4,155 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 2 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011576 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum interleukin-6 concentration 10,798 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST011575 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum interleukin-6 concentration in non-visceral-obese individuals 7,251 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST011574 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum interleukin-6 concentration in high fat diet 7,873 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST011573 Genome-wide genotyping array 2021-04-30 32928877 Jung SY 2020-09-14 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/32928877 Genome-wide association analysis of pro-inflammatory cytokines and gene-lifestyle interaction for invasive breast cancer risk: the WHI dbGaP Study. Serum interleukin-6 concentration in active individuals 4,221 European ancestry women NA Affymetrix, Illumina [21784812] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST011572 Genome-wide genotyping array 2021-03-26 33017352 Kim SK 2020-10-01 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/33017352 A Genome-wide Association Study for Concussion Risk. Concussion 4,064 European ancestry cases, 291,472 European ancestry controls NA Affymetrix [7743986] (imputed) 2 concussion http://www.ebi.ac.uk/efo/EFO_0011023 GCST011408 Genome-wide genotyping array 2021-06-16 33011741 Steggink LC 2020-10-03 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33011741 Genome-wide association study of cardiovascular disease in testicular cancer patients treated with platinum-based chemotherapy. cardiovascular disease in testicular cancer treated with platinum-based chemotherapy 53 cases, 322 controls NA Illumina [237087] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST011907 Genome-wide genotyping array 2021-07-08 33002439 Jin G 2020-10-01 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/33002439 Genetic risk, incident gastric cancer, and healthy lifestyle: a meta-analysis of genome-wide association studies and prospective cohort study. Gastric cancer 10,254 Han Chinese ancestry cases, 10,914 Han Chinese ancestry controls NA Affymetrix, Illumina [6957974] (imputed) 35 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST012016 Genome-wide genotyping array 2018-09-17 29844566 Davies G 2018-05-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29844566 Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. Reaction time 330,069 European ancestry individuals NA Affymetrix [805426] (imputed) 532 reaction time measurement http://www.ebi.ac.uk/efo/EFO_0008393 GCST006268 Genome-wide genotyping array 2018-09-17 29844566 Davies G 2018-05-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29844566 Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. General cognitive ability up to 300,486 European ancestry individuals NA Affymetrix, Illumina [at least 2500000] (imputed) 1248 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST006269 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine and/or diastolic blood pressure 757,601 European ancestry individuals with blood pressure measurements, 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 20 migraine disorder, diastolic blood pressure http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0006336 GCST011064 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine and/or systolic blood pressure 757,601 European ancestry individuals with blood pressure measurements, 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 16 migraine disorder, systolic blood pressure http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0006335 GCST011063 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine and/or pulse pressure 757,601 European ancestry individuals with blood pressure measurements, 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 20 migraine disorder, pulse pressure measurement http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0005763 GCST011062 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine with aura and/or diastolic blood pressure 757,601 European ancestry individuals with blood pressure measurements, up to 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 2 migraine with aura, diastolic blood pressure http://purl.obolibrary.org/obo/MONDO_0005475, http://www.ebi.ac.uk/efo/EFO_0006336 GCST011061 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine with aura and/or systolic blood pressure 757,601 European ancestry individuals with blood pressure measurements, up to 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 2 migraine with aura, systolic blood pressure http://purl.obolibrary.org/obo/MONDO_0005475, http://www.ebi.ac.uk/efo/EFO_0006335 GCST011060 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine with aura and/or pulse pressure 757,601 European ancestry individuals with blood pressure measurements, up to 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 2 pulse pressure measurement, migraine with aura http://www.ebi.ac.uk/efo/EFO_0005763, http://purl.obolibrary.org/obo/MONDO_0005475 GCST011059 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine without aura and/or diastolic blood pressure 757,601 European ancestry individuals with blood pressure measurements, up to 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 5 migraine without aura, susceptibility to, 4, diastolic blood pressure http://purl.obolibrary.org/obo/MONDO_0011847, http://www.ebi.ac.uk/efo/EFO_0006336 GCST011058 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine without aura and/or systolic blood pressure 757,601 European ancestry individuals with blood pressure measurements, up to 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 3 migraine without aura, susceptibility to, 4, systolic blood pressure http://purl.obolibrary.org/obo/MONDO_0011847, http://www.ebi.ac.uk/efo/EFO_0006335 GCST011057 Genome-wide genotyping array 2021-02-03 32632093 Guo Y 2020-07-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32632093 A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine. Migraine without aura and/or pulse pressure 757,601 European ancestry individuals with blood pressure measurements, up to 59,674 European ancestry migraine cases, 316,078 European ancestry controls NA NR [up to 7000000] 6 pulse pressure measurement, migraine without aura, susceptibility to, 4 http://www.ebi.ac.uk/efo/EFO_0005763, http://purl.obolibrary.org/obo/MONDO_0011847 GCST011056 Genome-wide genotyping array 2021-06-15 33239672 Laisk T 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239672 The genetic architecture of sporadic and multiple consecutive miscarriage. Sporadic miscarriage 49,996 European ancestry cases, 174,109 European ancestry controls NA Affymetrix, Illumina [9088459] (imputed) 1 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST011888 Genome-wide genotyping array 2021-06-15 33239672 Laisk T 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239672 The genetic architecture of sporadic and multiple consecutive miscarriage. Multiple consecutive miscarriage 750 European ancestry cases, 150,215 European ancestry controls NA Affymetrix, Illumina [8956145] (imputed) 4 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST011887 Genome-wide genotyping array 2021-06-15 33239672 Laisk T 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239672 The genetic architecture of sporadic and multiple consecutive miscarriage. Sporadic miscarriage 273 African ancestry cases, 2,919 African American cases, 390 Caribbean ancestry cases, 8,997 Chinese ancestry cases, 49,996 European ancestry cases, 1,151 Hispanic American cases, 511 South Asian ancestry cases, 482 African ancestry controls, 4,546 African American controls, 957 Caribbean ancestry controls, 126,723 Chinese ancestry controls, 174,109 European ancestry controls, 2,195 Hispanic American controls, 1,424 South Asian ancestry controls NA Affymetrix, Illumina [8664066] (imputed) 1 fertility measurement http://www.ebi.ac.uk/efo/EFO_0006923 GCST011889 Genome-wide genotyping array, Genome-wide sequencing 2021-02-28 32693751 Keene KL 2020-07-22 Stroke www.ncbi.nlm.nih.gov/pubmed/32693751 Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke. Stroke 3,734 African ancestry cases, 18,317 African ancestry controls NA Affymetrix, Illumina [~ 16900000] (imputed) 26 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST011176 Genome-wide genotyping array 2020-06-04 29514802 Leonard D 2018-03-07 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29514802 Novel gene variants associated with cardiovascular disease in systemic lupus erythematosus and rheumatoid arthritis. Cardiovascular disease in systemic lupus erythematosus 133 European ancestry cases, 681 Europen ancestry controls 84 European ancestry cases, 959 European ancestry controls Illumina [137213] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST010044 Targeted genotyping array [ImmunoChip] 2021-03-30 32824824 Diaz-Pena R 2020-08-18 J Pers Med www.ncbi.nlm.nih.gov/pubmed/32824824 Amerindian Ancestry Influences Genetic Susceptibility to Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease 214 Chilean cases, 193 Chilean controls NA Illumina [754159] (imputed) 3 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST011435 Genome-wide genotyping array 2021-03-12 33021770 Freidin MB 2020-09-30 Pain www.ncbi.nlm.nih.gov/pubmed/33021770 Sex- and age-specific genetic analysis of chronic back pain. Chronic back pain 35,705 European ancestry male cases, 166,372 European ancestry male controls 10,723 European ancestry male cases, 33,017 European ancestry male controls Affymetrix [14828942] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST011262 Genome-wide genotyping array 2021-03-12 33021770 Freidin MB 2020-09-30 Pain www.ncbi.nlm.nih.gov/pubmed/33021770 Sex- and age-specific genetic analysis of chronic back pain. Chronic back pain 7,758 European ancestry male cases, 36,074 European ancestry male controls NA Affymetrix [14828942] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST011261 Genome-wide genotyping array 2021-03-12 33021770 Freidin MB 2020-09-30 Pain www.ncbi.nlm.nih.gov/pubmed/33021770 Sex- and age-specific genetic analysis of chronic back pain. Chronic back pain 28,009 European ancestry male cases, 130,236 European ancestry male controls NA Affymetrix [14828942] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST011260 Genome-wide genotyping array 2021-03-12 33021770 Freidin MB 2020-09-30 Pain www.ncbi.nlm.nih.gov/pubmed/33021770 Sex- and age-specific genetic analysis of chronic back pain. Chronic back pain 43,230 European ancestry female cases, 194,524 European ancestry female controls 15,139 European ancestry female cases, 34,926 European ancestry female controls Affymetrix [14828942] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST011259 Genome-wide genotyping array 2021-03-12 33021770 Freidin MB 2020-09-30 Pain www.ncbi.nlm.nih.gov/pubmed/33021770 Sex- and age-specific genetic analysis of chronic back pain. Chronic back pain 8,987 European ancestry female cases, 35,502 European ancestry female controls NA Affymetrix [14828942] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST011258 Genome-wide genotyping array 2021-03-12 33021770 Freidin MB 2020-09-30 Pain www.ncbi.nlm.nih.gov/pubmed/33021770 Sex- and age-specific genetic analysis of chronic back pain. Chronic back pain 34,207 European ancestry female cases, 159,058 European ancestry female controls NA Affymetrix [14828942] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST011257 Genome-wide genotyping array 2020-10-06 29715290 Traylor M 2018-05-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/29715290 Exome array analysis of adverse reactions to fluoropyrimidine-based therapy for gastrointestinal cancer. Adverse response to chemotherapy (fluoropyrimidines) 504 European ancestry cases NA Illumina [59277] 0 response to fluoropyrimidines http://www.ebi.ac.uk/efo/EFO_0010825 GCST010639 Exome genotyping array [Exome array] 2020-07-16 31136621 van de Putte R 2019-05-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/31136621 Exome chip association study excluded the involvement of rare coding variants with large effect sizes in the etiology of anorectal malformations. Anorectal malformation 568 European ancestry cases, 1,860 European ancestry controls NA Illumina [239042] 13 anorectal malformation http://purl.obolibrary.org/obo/MONDO_0019938 GCST010206 Exome genotyping array [Exome array] 2020-07-06 31937794 Kim YW 2020-01-14 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31937794 Exploring the Novel Susceptibility Gene Variants for Primary Open-Angle Glaucoma in East Asian Cohorts: The GLAU-GENDISK Study. Glaucoma (primary open-angle) 309 Korean ancestry cases, 5,400 Korean ancestry controls 875 East Asian ancestry cases, 6,716 East Asian ancestry controls Illumina [63880] 1 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST010119 Exome genotyping array [Exome array] 2019-02-15 27818178 Hill WD 2016-11-03 Curr Biol www.ncbi.nlm.nih.gov/pubmed/27818178 Molecular Genetic Contributions to Social Deprivation and Household Income in UK Biobank. Household income 96,900 British ancestry individuals NA Affymetrix [~ 17300000] (imputed) 2 household income http://www.ebi.ac.uk/efo/EFO_0009695 GCST007155 Genome-wide genotyping array 2019-02-15 27818178 Hill WD 2016-11-03 Curr Biol www.ncbi.nlm.nih.gov/pubmed/27818178 Molecular Genetic Contributions to Social Deprivation and Household Income in UK Biobank. Social deprivation 112,005 British ancestry individuals NA Affymetrix [~ 17300000] (imputed) 0 social deprivation http://www.ebi.ac.uk/efo/EFO_0009696 GCST007156 Genome-wide genotyping array 2021-02-12 33338273 Im C 2020-12-18 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/33338273 Genome-wide Association Studies Reveal Novel Locus With Sex-/Therapy-Specific Fracture Risk Effects in Childhood Cancer Survivors. First fracture in long-term childhood cancer survivors (time to event) 1,164 European ancestry males 771 European ancestry males Illumina [~ 5400000] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST011111 Genome-wide genotyping array 2021-02-12 33338273 Im C 2020-12-18 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/33338273 Genome-wide Association Studies Reveal Novel Locus With Sex-/Therapy-Specific Fracture Risk Effects in Childhood Cancer Survivors. First fracture in long-term childhood cancer survivors (time to event) 1,289 European ancestry females 646 European ancestry females Illumina [~ 5400000] (imputed) 1 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST011110 Genome-wide genotyping array 2021-02-12 33338273 Im C 2020-12-18 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/33338273 Genome-wide Association Studies Reveal Novel Locus With Sex-/Therapy-Specific Fracture Risk Effects in Childhood Cancer Survivors. First fracture in long-term childhood cancer survivors (time to event) 1,289 European ancestry females, 1,164 European ancestry males 646 European ancestry females, 771 European ancestry males Illumina [~ 5400000] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST011112 Genome-wide genotyping array 2020-09-10 32492095 Zhou H 2020-06-03 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/32492095 Association of OPRM1 Functional Coding Variant With Opioid Use Disorder: A Genome-Wide Association Study. Opioid use disorder 10,544 European ancestry cases, 72,163 European ancestry controls, 5,212 African American cases, 26,876 African American controls 748 European ancestry cases, 361,107 European ancestry controls Affymetrix [9420000] (imputed) 1 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST010510 Genome-wide genotyping array 2019-03-26 30642921 de Vries PS 2019-01-14 Blood www.ncbi.nlm.nih.gov/pubmed/30642921 A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology. Factor VII activity or levels 24,075 European ancestry individuals, 3,420 African American individuals NA Affymetrix, Illumina [10044948] (imputed) 6 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST007402 Genome-wide genotyping array 2019-03-26 30642921 de Vries PS 2019-01-14 Blood www.ncbi.nlm.nih.gov/pubmed/30642921 A genome-wide association study identifies new loci for factor VII and implicates factor VII in ischemic stroke etiology. Factor VII activity 20,014 European ancestry individuals, 3,420 African American individuals NA Affymetrix, Illumina [10044948] (imputed) 36 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST007401 Genome-wide genotyping array 2021-08-13 33536081 Hu J 2021-02-03 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/33536081 Genetic variants are identified to increase risk of COVID-19 related mortality from UK Biobank data. Mortality in COVID-19 292 European ancestry cases, 804 European ancestry controls NA NR [18617478] (imputed) 12 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST012192 Genome-wide genotyping array 2021-12-07 31343553 Pickering C 2019-07-22 J Strength Cond Res www.ncbi.nlm.nih.gov/pubmed/31343553 A Genome-Wide Association Study of Sprint Performance in Elite Youth Football Players. Sprint performance 48 European ancestry individuals 126 European ancestry individuals Affymetrix [> 600000] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST012581 Genome-wide genotyping array 2021-08-13 33517400 Ahluwalia TS 2021-01-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33517400 Genome-Wide Association Study of Circulating Interleukin 6 Levels Identifies Novel Loci. Interleukin-6 levels 52,654 European ancestry individuals 14,774 European ancestry individuals Affymetrix, Illumina, Perlegen [2454025] (imputed) 9 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST012198 Genome-wide genotyping array 2019-08-28 31194737 Johnston KJA 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194737 Genome-wide association study of multisite chronic pain in UK Biobank. Chronic widespread pain 6,815 British ancestry cases, 10,000 British ancestry controls NA NR [NR] 0 chronic widespread pain http://www.ebi.ac.uk/efo/EFO_0010099 GCST008511 Genome-wide genotyping array 2019-08-28 31194737 Johnston KJA 2019-06-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31194737 Genome-wide association study of multisite chronic pain in UK Biobank. Multisite chronic pain 387,649 British ancestry individuals NA NR [NR] 39 multisite chronic pain http://www.ebi.ac.uk/efo/EFO_0010100 GCST008512 Genome-wide genotyping array 2022-11-25 31349112 Miron J 2019-07-02 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/31349112 Association of PPP2R1A with Alzheimer's disease and specific cognitive domains. Alzheimer's disease 751 European ancestry cases, 751 European ancestry controls 17,008 European ancestry cases, 37,154 European ancestry controls Illumina [491456] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST013076 Genome-wide genotyping array 2020-08-22 32794382 Cho SB 2020-07-28 Diabetes Metab J www.ncbi.nlm.nih.gov/pubmed/32794382 Exome Chip Analysis of 14,026 Koreans Reve-als Known and Newly Discovered Genetic Loci Associated with Type 2 Diabetes Mellitus. Type 2 diabetes 14,026 Korean ancestry individuals NA Illumina [up to 242901] 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST010436 Exome genotyping array [Exome array] 2022-10-13 32782260 Elvsashagen T 2020-08-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32782260 The genetic architecture of human brainstem structures and their involvement in common brain disorders. Brainstem volume 27,034 European ancestry individuals 7,432 European ancestry individuals NR [NR] (imputed) 0 brain stem volume measurement http://www.ebi.ac.uk/efo/EFO_0010605 GCST013021 Genome-wide genotyping array 2022-10-13 32782260 Elvsashagen T 2020-08-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32782260 The genetic architecture of human brainstem structures and their involvement in common brain disorders. Midbrain volume 27,034 European ancestry individuals 7,432 European ancestry individuals NR [NR] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST013017 Genome-wide genotyping array 2022-10-13 32782260 Elvsashagen T 2020-08-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32782260 The genetic architecture of human brainstem structures and their involvement in common brain disorders. Pons volume 27,034 European ancestry individuals 7,432 European ancestry individuals NR [NR] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST013018 Genome-wide genotyping array 2022-10-13 32782260 Elvsashagen T 2020-08-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32782260 The genetic architecture of human brainstem structures and their involvement in common brain disorders. Superior cerebellar peduncle volume 27,034 European ancestry individuals 7,432 European ancestry individuals NR [NR] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST013019 Genome-wide genotyping array 2022-10-13 32782260 Elvsashagen T 2020-08-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32782260 The genetic architecture of human brainstem structures and their involvement in common brain disorders. Medulla oblongata volume 27,034 European ancestry individuals 7,432 European ancestry individuals NR [NR] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST013020 Genome-wide genotyping array 2019-08-23 31358989 Gelernter J 2019-07-29 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/31358989 Genome-wide association study of post-traumatic stress disorder reexperiencing symptoms in >165,000 US veterans. Post-traumatic stress disorder (re-experiencing symptoms) 146,660 European ancestry individuals, 19,983 African American individuals 117,900 European ancestry individuals Affymetrix [49134253] (imputed) 16 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST008490 Genome-wide genotyping array 2021-04-21 32785646 Maguire S 2020-08-12 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/32785646 Common susceptibility loci for male breast cancer. Breast cancer (male) 1,380 European ancestry cases, 3,620 European ancestry controls 810 European ancestry cases, 1,026 European ancestry controls Illumina [8074073] (imputed) 7 male breast carcinoma http://www.ebi.ac.uk/efo/EFO_0006861 GCST011526 Genome-wide genotyping array 2019-08-07 31095341 Kerns SL 2019-05-16 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/31095341 Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy. Toxicity response to radiotherapy in prostate cancer (rectal bleeding) (time to event) 3,379 European ancestry individuals NA Affymetrix, Illumina [~ 6000000] (imputed) 14 Hematochezia, response to radiation http://purl.obolibrary.org/obo/HP_0002573, http://purl.obolibrary.org/obo/GO_0009314 GCST008381 Genome-wide genotyping array 2019-08-07 31095341 Kerns SL 2019-05-16 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/31095341 Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy. Toxicity response to radiotherapy in prostate cancer (decreased urine stream) (time to event) 3,470 European ancestry individuals NR Affymetrix, Illumina [~ 6000000] (imputed) 12 response to radiation, Urinary retention http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0000016 GCST008378 Genome-wide genotyping array 2019-08-07 31095341 Kerns SL 2019-05-16 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/31095341 Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy. Toxicity response to radiotherapy in prostate cancer (hematuria) (time to event) 3,619 European ancestry individuals 538 Japanese ancestry individuals Affymetrix, Illumina [~ 6000000] (imputed) 16 response to radiation, Hematuria http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0000790 GCST008380 Genome-wide genotyping array 2019-08-07 31095341 Kerns SL 2019-05-16 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/31095341 Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy. Response to radiotherapy in prostate cancer (overall toxicity) 3,871 European ancestry individuals NA Affymetrix, Illumina [~ 6000000] (imputed) 3 response to radiation, adverse effect http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0009658 GCST008379 Genome-wide genotyping array 2019-08-07 31095341 Kerns SL 2019-05-16 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/31095341 Radiogenomics Consortium Genome-Wide Association Study Meta-analysis of Late Toxicity after Prostate Cancer Radiotherapy. Toxicity response to radiotherapy in prostate cancer (increased urinary frequency) (time to event) 3,782 European ancestry individuals NA Affymetrix, Illumina [~ 6000000] (imputed) 6 response to radiation, Abnormality of the urinary system http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0000079 GCST008382 Genome-wide genotyping array 2021-07-15 33545615 Hsu LA 2021-01-19 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/33545615 Circulating chemerin levels are determined through circulating platelet counts in nondiabetic Taiwanese people: A bidirectional Mendelian randomization study. Platelet count 17,037 Han Chinese ancestry individuals NA Affymetrix [603527] 11 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST012032 Genome-wide genotyping array 2021-07-15 33545615 Hsu LA 2021-01-19 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/33545615 Circulating chemerin levels are determined through circulating platelet counts in nondiabetic Taiwanese people: A bidirectional Mendelian randomization study. Chemerin levels 3,887 Han Chinese ancestry individuals NA Affymetrix [610203] 2 chemerin measurement http://www.ebi.ac.uk/efo/EFO_0004573 GCST012031 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Type 2 diabetes 148,726 European ancestry cases, 24,646 African American cases, 8,616 Hispanic cases, 46,511 Asian ancestry cases, 965,732 European ancestry controls, 31,446 African American controls, 11,829 Hispanic controls, 169,776 Asian ancestry controls NA Affymetrix, Illumina [at least 945603] (imputed) 558 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST010557 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Type 2 diabetes 24,646 African American cases, 31,446 African American controls NA Affymetrix, Illumina [945603] (imputed) 28 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST010556 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Type 2 diabetes 148,726 European ancestry cases, 965,732 European ancestry controls NA Affymetrix, Illumina [1198787] (imputed) 658 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST010555 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Type 2 diabetes 8,616 Hispanic cases, 11,829 Hispanic controls NA Affymetrix, Illumina [1077427] (imputed) 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST010554 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Type 2 diabetes 46,511 Asian ancestry cases, 169,776 Asian ancestry controls NA Affymetrix, Illumina [1077427] (imputed) 86 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST010553 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Chronic kidney disease x type 2 diabetes interaction 67,403 European ancestry cases, 129,827 European ancestry controls NA Affymetrix [at least 723305] (imputed) 2 chronic kidney disease, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0003884, http://purl.obolibrary.org/obo/MONDO_0005148 GCST010552 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Peripheral arterial disease x type 2 diabetes interaction 5,882 European ancestry cases, 161,348 European ancestry controls NA Affymetrix [at least 723305] (imputed) 1 type 2 diabetes mellitus, peripheral arterial disease http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0004265 GCST010549 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Coronary heart disease x type 2 diabetes interaction 56,285 European ancestry coronary heart disease cases, 140,945 European ancestry controls NA Affymetrix [at least 723305] (imputed) 3 type 2 diabetes mellitus, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0001645 GCST010551 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Acute ischemic stroke x type 2 diabetes interaction 11,796 European ancestry cases, 178,481 European ancestry controls NA Affymetrix [at least 723305] (imputed) 2 Ischemic stroke, type 2 diabetes mellitus http://purl.obolibrary.org/obo/HP_0002140, http://purl.obolibrary.org/obo/MONDO_0005148 GCST010550 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Retinopathy x type 2 diabetes interaction 13,881 European ancestry cases, 123,538 European ancestry controls NA Affymetrix [at least 723305] (imputed) 4 retinopathy, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0003839, http://purl.obolibrary.org/obo/MONDO_0005148 GCST010548 Genome-wide genotyping array 2020-09-14 32541925 Vujkovic M 2020-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32541925 Discovery of 318 new risk loci for type 2 diabetes and related vascular outcomes among 1.4 million participants in a multi-ancestry meta-analysis. Neuropathy x type 2 diabetes interaction 40,475 European ancestry cases, 110,331 European ancestry controls NA Affymetrix [at least 723305] (imputed) 1 neuropathy, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0004149, http://purl.obolibrary.org/obo/MONDO_0005148 GCST010547 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Adult onset asthma and/or BMI 33,418 European ancestry cases, 393,186 European ancestry controls, 31,218 European ancestry individuals NA Affymetrix [~ 8270000] (imputed) 8 adult onset asthma, body mass index http://www.ebi.ac.uk/efo/EFO_1002011, http://www.ebi.ac.uk/efo/EFO_0004340 GCST009868 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Nonatopic asthma and/or BMI 28,862 European ancestry cases, 422,048 European ancestry controls, 6,912 European ancestry individuals NA Affymetrix [~ 8270000] (imputed) 10 asthma, body mass index http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0004340 GCST009866 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Adult onset asthma and/or waist-to-hip ratio adjusted for BMI 33,418 European ancestry cases, 393,186 European ancestry controls, 31,086 European ancestry individuals NA Affymetrix [~ 8270000] (imputed) 6 BMI-adjusted waist-hip ratio, adult onset asthma http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_1002011 GCST009865 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Nonatopic asthma and/or waist-to-hip ratio adjusted for BMI 28,862 European ancestry cases, 422,048 European ancestry controls, 6,780 European ancestry individuals NA Affymetrix [~ 8270000] (imputed) 8 BMI-adjusted waist-hip ratio, asthma http://www.ebi.ac.uk/efo/EFO_0007788, http://purl.obolibrary.org/obo/MONDO_0004979 GCST009862 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Adult onset asthma or type 2 diabetes 33,418 European ancestry asthma cases, 393,186 European ancestry asthma controls, 159,208 European ancestry diabetes cases and controls NA Affymetrix [up to 8270000] (imputed) 6 adult onset asthma, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_1002011, http://purl.obolibrary.org/obo/MONDO_0005148 GCST009859 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Nonatopic asthma or type 2 diabetes 28,862 European ancestry asthma cases, 422,048 European ancestry asthma controls, 159,208 European ancestry diabetes cases and controls NA Affymetrix [up to 8270000] (imputed) 5 asthma, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0004979, http://purl.obolibrary.org/obo/MONDO_0005148 GCST009857 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Adult onset asthma or fasting insulin levels 33,418 European ancestry cases, 393,186 European ancestry controls, 51,750 European ancestry individuals NA Affymetrix [~ 7660000] (imputed) 0 adult onset asthma, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_1002011, http://www.ebi.ac.uk/efo/EFO_0004466 GCST009855 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Nonatopic asthma or fasting insulin levels 28,862 European ancestry cases, 422,048 European ancestry controls, 51,750 European ancestry individuals NA Affymetrix [~ 7660000] (imputed) 0 asthma, fasting blood insulin measurement http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0004466 GCST009851 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Adult onset asthma or fasting glucose levels 33,418 European ancestry cases, 393,186 European ancestry controls, 58,047 European ancestry individuals NA Affymetrix [~ 7660000] (imputed) 1 adult onset asthma, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_1002011, http://www.ebi.ac.uk/efo/EFO_0004465 GCST009848 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Nonatopic asthma or fasting glucose levels 28,862 European ancestry cases, 422,048 European ancestry controls, 58,047 European ancestry individuals NA Affymetrix [~ 7660000] (imputed) 1 asthma, fasting blood glucose measurement http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0004465 GCST009843 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Asthma (adult onset) 33,418 European ancestry cases, 393,186 European ancestry controls NA Affymetrix [~ 8270000] (imputed) 86 adult onset asthma http://www.ebi.ac.uk/efo/EFO_1002011 GCST009842 Genome-wide genotyping array 2020-09-03 32469254 Matsunaga H 2020-05-29 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32469254 Transethnic Meta-analysis of Genome-wide Association Studies Identifies Three New Loci and Characterizes Population-specific Differences for Coronary Artery Disease. Coronary artery disease 15,302 Japanese ancestry cases, 36,140 Japanese ancestry controls NA Illumina [5932413] (imputed) 23 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST010480 Genome-wide genotyping array 2020-09-03 32469254 Matsunaga H 2020-05-29 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32469254 Transethnic Meta-analysis of Genome-wide Association Studies Identifies Three New Loci and Characterizes Population-specific Differences for Coronary Artery Disease. Coronary artery disease 15,302 Japanese ancestry cases, 76,014 European and East Asian ancestry cases, 36,140 Japanese ancestry controls, 264,785 European and East Asian ancestry controls NA Illumina [5167567] (imputed) 76 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST010479 Genome-wide genotyping array 2020-07-22 32276964 Shete S 2020-04-10 Cancer Res www.ncbi.nlm.nih.gov/pubmed/32276964 A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck. Oral cavity cancer 631 European ancestry cases, 4,493 European ancestry controls 2,568 European ancestry cases, 3,232 European ancestry controls Illumina [7858089] (imputed) 2 oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0005570 GCST010287 Genome-wide genotyping array 2020-07-22 32276964 Shete S 2020-04-10 Cancer Res www.ncbi.nlm.nih.gov/pubmed/32276964 A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck. Oropharynx cancer 1,144 European ancestry cases, 4,493 European ancestry controls 2,328 European ancestry cases, 3,232 European ancestry controls Illumina [7858089] (imputed) 3 oropharynx cancer http://www.ebi.ac.uk/efo/EFO_1001931 GCST010286 Genome-wide genotyping array 2020-07-22 32276964 Shete S 2020-04-10 Cancer Res www.ncbi.nlm.nih.gov/pubmed/32276964 A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck. Hypopharyngeal or laryngeal cancer 394 European ancestry cases, 4,493 European ancestry controls 295 European ancestry cases, 3,232 European ancestry controls Illumina [7858089] (imputed) 2 laryngeal squamous cell carcinoma, hypopharynx cancer http://www.ebi.ac.uk/efo/EFO_0006352, http://www.ebi.ac.uk/efo/EFO_0007321 GCST010285 Genome-wide genotyping array 2020-07-22 32276964 Shete S 2020-04-10 Cancer Res www.ncbi.nlm.nih.gov/pubmed/32276964 A genome-wide association study identifies two novel susceptible regions for squamous cell carcinoma of the head and neck. Head and neck squamous cell carcinoma 2,171 European ancestry cases, 4,493 European ancestry controls 5,205 European ancestry cases, 3,232 European ancestry controls Illumina [7858089] (imputed) 3 head and neck squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000181 GCST010288 Genome-wide genotyping array 2021-03-22 33536631 Bell S 2021-02-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33536631 A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis. Iron status biomarkers (ferritin levels) 246,139 European ancestry individuals NA Affymetrix, Illumina [40000000] (imputed) 39 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST011369 Genome-wide genotyping array 2021-03-22 33536631 Bell S 2021-02-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33536631 A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis. Iron status biomarkers (total iron binding capacity) 135,430 European ancestry individuals NA Affymetrix, Illumina [40000000] (imputed) 14 total iron binding capacity http://www.ebi.ac.uk/efo/EFO_0006334 GCST011368 Genome-wide genotyping array 2021-03-22 33536631 Bell S 2021-02-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33536631 A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis. Iron status biomarkers (iron levels) 163,511 European ancestry individuals NA Affymetrix, Illumina [40000000] (imputed) 13 serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006332 GCST011367 Genome-wide genotyping array 2021-03-22 33536631 Bell S 2021-02-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33536631 A genome-wide meta-analysis yields 46 new loci associating with biomarkers of iron homeostasis. Iron status biomarkers (transferrin saturation) 131,471 European ancestry individuals NA Affymetrix, Illumina [40000000] (imputed) 9 transferrin saturation measurement http://www.ebi.ac.uk/efo/EFO_0006333 GCST011366 Genome-wide genotyping array 2020-08-25 32766473 Yoshida K 2020-05-19 Hepatol Commun www.ncbi.nlm.nih.gov/pubmed/32766473 Genome-Wide Association Study of Lean Nonalcoholic Fatty Liver Disease Suggests Human Leukocyte Antigen as a Novel Candidate Locus. Lean nonalcoholic fatty liver disease 275 Japanese ancestry cases, 1,411 Japanese ancestry controls NA Affymetrix [NR] 4 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST010460 Genome-wide genotyping array 2018-12-03 28196072 Hagenaars SP 2017-02-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28196072 Genetic prediction of male pattern baldness. Male-pattern baldness 52,874 British ancestry males NR [NR] (imputed) 335 alopecia http://purl.obolibrary.org/obo/MONDO_0004907 GCST006661 Genome-wide genotyping array 2021-08-13 33531474 Burton CL 2021-02-02 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33531474 Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder. Obsessive-compulsive traits 5,018 European ancestry children and adolescents NA Illumina [7870334] (imputed) 15 Obsessive-compulsive trait http://purl.obolibrary.org/obo/HP_0008770 GCST012194 Genome-wide genotyping array 2021-08-13 33531474 Burton CL 2021-02-02 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33531474 Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder. Obsessive-compulsive disorder 3,369 European ancestry cases, 8,611 European ancestry controls NA Illumina [NR] (imputed) 0 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST012193 Genome-wide genotyping array 2021-08-13 33539483 Li Z 2021-02-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/33539483 Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins. Body mass index and systolic blood pressure (bivariate analysis) 274 Chinese ancestry dizygotic twins NA Illumina [7401356] (imputed) 13 systolic blood pressure, body mass index http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004340 GCST012191 Genome-wide genotyping array 2021-08-13 33539483 Li Z 2021-02-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/33539483 Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins. Body mass index and diastolic blood pressure (bivariate analysis) 274 Chinese ancestry dizygotic twins NA Illumina [7401356] (imputed) 13 diastolic blood pressure, body mass index http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004340 GCST012190 Genome-wide genotyping array 2021-08-13 33539483 Li Z 2021-02-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/33539483 Bivariate genome-wide association study (GWAS) of body mass index and blood pressure phenotypes in northern Chinese twins. Systolic blood pressure and diastolic blood pressure (bivariate analysis) 274 Chinese ancestry dizygotic twins NA Illumina [7401356] (imputed) 17 diastolic blood pressure, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335 GCST012189 Genome-wide genotyping array 2021-03-22 33532862 Hartiala JA 2021-02-03 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/33532862 Genome-wide analysis identifies novel susceptibility loci for myocardial infarction. Myocardial infarction 14,825 European ancestry cases, 44,000 European and unknown ancestry cases, 2,680 cases, 380,970 European ancestry controls, 123,504 European and unknown ancestry controls, 73,242 controls NA NR [8126035] (imputed) 159 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST011365 Genome-wide genotyping array 2021-03-22 33532862 Hartiala JA 2021-02-03 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/33532862 Genome-wide analysis identifies novel susceptibility loci for myocardial infarction. Myocardial infarction 14,825 European ancestry cases, 2,680 cases, 380,970 European ancestry controls, 73,242 controls NA NR [10903881] (imputed) 31 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST011364 Genome-wide genotyping array 2021-01-26 32193507 Fan Q 2020-03-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32193507 Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Corneal curvature 29,580 European ancestry individuals, 14,462 Asian ancestry individuals 88,218 European ancestry individuals Affymetrix, Illumina [8936601] (imputed) 41 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST90012795 Genome-wide genotyping array 2021-01-26 32193507 Fan Q 2020-03-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32193507 Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Corneal curvature 29,580 European ancestry individuals NA Affymetrix, Illumina [8936601] (imputed) 32 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST90012796 Genome-wide genotyping array 2021-01-26 32193507 Fan Q 2020-03-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32193507 Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Corneal curvature 14,462 Asian ancestry individuals NA Affymetrix, Illumina [7861976] (imputed) 11 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST90012797 Genome-wide genotyping array 2021-01-26 32193507 Fan Q 2020-03-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32193507 Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Corneal curvature 8,620 individuals (<25 years old) NA Affymetrix, Illumina [8936601] (imputed) 6 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST90012798 Genome-wide genotyping array 2021-01-26 32193507 Fan Q 2020-03-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32193507 Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error. Corneal curvature 35,422 individuals (>=25 years old) NA Affymetrix, Illumina [8936601] (imputed) 40 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST90012799 Genome-wide genotyping array 2021-02-19 33547301 Chen VL 2021-02-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33547301 Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology. Alanine aminotransferase levels 390,812 European ancestry individuals 134,154 East Asian ancestry individuals Affymetrix [4312306] (imputed) 172 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90011898 Genome-wide genotyping array 2021-02-19 33547301 Chen VL 2021-02-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33547301 Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology. Aspartate aminotransferase levels 389,565 European ancestry individuals 134,182 East Asian ancestry individuals Affymetrix [4314223] (imputed) 199 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90011899 Genome-wide genotyping array 2021-02-19 33547301 Chen VL 2021-02-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33547301 Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology. Serum alkaline phosphatase levels 390,964 European ancestry individuals 105,030 East Asian ancestry individuals Affymetrix [4311822] (imputed) 216 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90011900 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number (white blood cells) 1,333 males NA Illumina [7369986] (imputed) 2 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007392 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number 3,647 European ancestry children NA Illumina [7410776] (imputed) 11 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007393 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number 2,102 European ancestry neonates NA Illumina [7361275] (imputed) 2 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007394 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number 5,461 European ancestry mothers NA Illumina [7360988] (imputed) 3 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007395 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number (white blood cells) 3,405 European ancestry mothers NA Illumina [7360988] (imputed) 2 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007396 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number (white blood cells) 1,338 females NA Illumina [7373492] (imputed) 1 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007397 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number (white blood cells) 3,405 European ancestry females, 1,338 females NA Illumina [up to 7373492] (imputed) 1 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007398 Genome-wide genotyping array 2019-03-25 30704525 Guyatt AL 2019-01-31 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30704525 A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. Mitochondrial DNA copy number 5,461 European ancestry females, 1,338 females NA Illumina [up to 7373492] (imputed) 2 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST007399 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Asthma (childhood onset) 13,435 European ancestry cases, 393,186 European ancestry controls NA Affymetrix [~ 8270000] (imputed) 219 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST009841 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Nonatopic asthma 28,862 European ancestry cases, 422,048 European ancestry controls NA Affymetrix [~ 8270000] (imputed) 109 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST009845 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Atopic asthma 23,982 European ancestry cases, 393,169 European ancestry controls NA Affymetrix [~ 8270000] (imputed) 198 atopic asthma http://www.ebi.ac.uk/efo/EFO_0010638 GCST009850 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Waist-to-hip ratio adjusted for BMI 457,690 European ancestry individuals NA Affymetrix [~ 8270000] (imputed) 1077 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST009858 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Waist circumference adjusted for body mass index 457,690 European ancestry individuals NA Affymetrix [~ 8270000] (imputed) 1260 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST009867 Genome-wide genotyping array 2020-04-17 31669095 Zhu Z 2019-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/31669095 Shared Genetic and Experimental Links between Obesity-Related Traits and Asthma Subtypes in UK Biobank. Body mass index 457,822 European ancestry individuals NA Affymetrix [~ 8270000] (imputed) 1644 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009871 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Brain morphology (MOSTest) 26,502 European ancestry individuals NA NR [7428630] (imputed) 346 brain measurement, neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004464, http://www.ebi.ac.uk/efo/EFO_0004346 GCST010703 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Cortical thickness (MOSTest) 26,502 European ancestry individuals NA NR [7428630] (imputed) 70 cortical thickness, neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004840, http://www.ebi.ac.uk/efo/EFO_0004346 GCST010700 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Subcortical volume (MOSTest) 26,502 European ancestry individuals NA NR [7428630] (imputed) 177 neuroimaging measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0004346, http://www.ebi.ac.uk/efo/EFO_0006930 GCST010702 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Brain morphology (min-P) 26,502 European ancestry individuals NA NR [7428630] (imputed) 113 brain measurement, neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004464, http://www.ebi.ac.uk/efo/EFO_0004346 GCST010699 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Cortical surface area (MOSTest) 26,502 European ancestry individuals NA NR [7428630] (imputed) 138 cortical surface area measurement, neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0010736, http://www.ebi.ac.uk/efo/EFO_0004346 GCST010701 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Subcortical volume (min-P) 26,502 European ancestry individuals NA NR [7428630] (imputed) 89 neuroimaging measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0004346, http://www.ebi.ac.uk/efo/EFO_0006930 GCST010698 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Cortical surface area (min-P) 26,502 European ancestry individuals NA NR [7428630] (imputed) 53 cortical surface area measurement, neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0010736, http://www.ebi.ac.uk/efo/EFO_0004346 GCST010697 Genome-wide genotyping array 2020-10-23 32665545 van der Meer D 2020-07-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32665545 Understanding the genetic determinants of the brain with MOSTest. Cortical thickness (min-P) 26,502 European ancestry individuals NA NR [7428630] (imputed) 23 cortical thickness, neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004840, http://www.ebi.ac.uk/efo/EFO_0004346 GCST010696 Genome-wide genotyping array 2021-02-10 33263727 Li HJ 2020-12-02 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/33263727 Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis. Bipolar disorder 1,822 Han Chinese ancestry cases, 4,650 Han Chinese ancestry controls 958 Han Chinese ancestry cases, 2,050 Han Chinese ancestry controls Illumina [4499546] (imputed) 2 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST011101 Genome-wide genotyping array 2021-02-10 33263727 Li HJ 2020-12-02 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/33263727 Novel Risk Loci Associated With Genetic Risk for Bipolar Disorder Among Han Chinese Individuals: A Genome-Wide Association Study and Meta-analysis. Bipolar disorder 1,822 Han Chinese ancestry cases, 4,650 Han Chinese ancestry controls, 20,352 European ancestry cases, 31,358 European ancestry controls NA Illumina [3742365] (imputed) 23 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST011102 Genome-wide genotyping array 2020-06-11 31591516 Ricano-Ponce I 2019-10-07 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31591516 Immunochip meta-analysis in European and Argentinian populations identifies two novel genetic loci associated with celiac disease. Celiac disease 12,567 European ancestry cases, 381 Hispanic cases, 14,013 European ancestry controls, 813 Hispanic controls NA Illumina [127855] 4 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST010064 Targeted genotyping array [ImmunoChip] 2019-08-20 31324766 Adeyemo AA 2019-07-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31324766 ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response. Type 2 diabetes 2,342 Sub-Saharan African ancestry cases, 2,889 Sub-Saharan African ancestry controls, 8,599 African American individuals NA Affymetrix, Illumina [~ 18000000] (imputed) 4 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST008464 Genome-wide genotyping array 2019-08-20 31324766 Adeyemo AA 2019-07-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31324766 ZRANB3 is an African-specific type 2 diabetes locus associated with beta-cell mass and insulin response. Type 2 diabetes 2,342 Sub-Saharan African ancestry cases, 2,889 Sub-Saharan African ancestry controls 1,602 South African Zulu ancestry cases, 976 South African Zulu ancestry controls Affymetrix, Illumina [~ 18000000] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST008463 Genome-wide genotyping array 2019-08-22 31346403 Massrali A 2019-07-17 Mol Autism www.ncbi.nlm.nih.gov/pubmed/31346403 Integrated genetic and methylomic analyses identify shared biology between autism and autistic traits. Autistic traits score (Social and Communication Disorders Checklist) 5,628 European ancestry children NA Illumina [8282911] (imputed) 0 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST008484 Genome-wide genotyping array 2021-02-08 31363184 Zhu Z 2019-07-30 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31363184 Heritability of human visual contour integration-an integrated genomic study. Visual contour integration 1,931 East Asian ancestry individuals 688 East Asian ancestry individuals Illumina [at least 830937] (imputed) 0 visual perception measurement http://www.ebi.ac.uk/efo/EFO_0009700 GCST011099 Genome-wide genotyping array 2019-08-22 31345160 Jia H 2019-07-26 BMC Genet www.ncbi.nlm.nih.gov/pubmed/31345160 GWAS of habitual coffee consumption reveals a sex difference in the genetic effect of the 12q24 locus in the Japanese population. Coffee consumption 6,264 Japanese ancestry individuals 5,975 Japanese ancestry individuals Illumina [5264155] (imputed) 3 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST008487 Genome-wide genotyping array 2019-03-28 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Rapid automised naming of digits 2,563 European ancestry individuals NA Illumina [6952813] (imputed) 17 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007469 Genome-wide genotyping array 2019-03-28 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Rapid automised naming of pictures 2,562 European ancestry individuals NA Illumina [6952813] (imputed) 15 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007473 Genome-wide genotyping array 2019-03-28 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Short-term memory (digit-span task) 2,591 European ancestry individuals NA Illumina [6952813] (imputed) 12 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST007471 Genome-wide genotyping array 2019-03-29 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Non-word reading 3,409 European ancestry individuals NA Illumina [6969139] (imputed) 23 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST007478 Genome-wide genotyping array 2019-03-28 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Word spelling 3,399 European ancestry individuals NA Illumina [6969139] (imputed) 19 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007467 Genome-wide genotyping array 2019-03-28 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Word reading 3,468 European ancestry individuals NA Illumina [6969139] (imputed) 17 word reading http://www.ebi.ac.uk/efo/EFO_0005300 GCST007466 Genome-wide genotyping array 2019-03-28 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Phoneme awareness 3,093 European ancestry individuals NA Illumina [6969139] (imputed) 17 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007465 Genome-wide genotyping array 2019-03-29 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Reading ability (multivariate) up to 3,468 European ancestry individuals NA Illumina [up to 6969139] (imputed) 28 reading http://www.ebi.ac.uk/efo/EFO_0005229 GCST007479 Genome-wide genotyping array 2019-03-28 30741946 Gialluisi A 2019-02-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30741946 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. Rapid automised naming of letters 2,563 European ancestry individuals NA Illumina [6952813] (imputed) 19 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST007470 Genome-wide genotyping array 2019-11-04 31341412 Chen QY 2019-06-10 Int J Med Sci www.ncbi.nlm.nih.gov/pubmed/31341412 Locus 5p13.1 may be associated with the selection of cancer-related HBV core promoter mutations. Viral basal core promoter double mutation in hepatitis B virus surface antigen (HBsAg) seropositivity 218 Chinese ancestry asymptomatic cases, 191 Chinese ancestry asymptomatic controls 203 Chinese ancestry asymptomatic cases, 181 Chinese ancestry asymptomatic controls Illumina [25296] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST009000 Genome-wide genotyping array 2019-12-03 31371054 Ruddy KJ 2019-07-29 Fertil Steril www.ncbi.nlm.nih.gov/pubmed/31371054 Genetic predictors of chemotherapy-related amenorrhea in women with breast cancer. Adverse response to chemotherapy (amenorrhea) in breast cancer 457 European ancestry amenorrheic cases, 711 European ancestry post-chemotherapy menses cases NA Illumina [5430816] (imputed) 10 amenorrhea, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0010269, http://purl.obolibrary.org/obo/GO_0097327 GCST009153 Genome-wide genotyping array 2019-09-24 31358974 Evangelou E 2019-07-29 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/31358974 New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders. Alcohol consumption 480,842 European ancestry individuals NA Affymetrix, Illumina [~ 7100000] (imputed) 51 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST008757 Genome-wide genotyping array 2019-09-02 31220337 Carr DF 2019-06-20 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31220337 Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink. Simvastatin-induced myopathy 85 European ancestry cases, 2,501 controls NA Illumina [654642] (imputed) 28 response to simvastatin, myopathy http://purl.obolibrary.org/obo/GO_1903491, http://www.ebi.ac.uk/efo/EFO_0004145 GCST008551 Genome-wide genotyping array 2019-09-02 31220337 Carr DF 2019-06-20 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31220337 Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink. Atorvastatin-induced myopathy 28 European ancestry cases, 2,501 controls NA Illumina [654642] (imputed) 9 response to atorvastatin, myopathy http://www.ebi.ac.uk/efo/EFO_0010124, http://www.ebi.ac.uk/efo/EFO_0004145 GCST008554 Genome-wide genotyping array 2019-09-02 31220337 Carr DF 2019-06-20 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31220337 Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink. Statin-induced myopathy (severe) 32 European ancestry cases, 2,501 controls NA Illumina [654642] (imputed) 6 response to statin, myopathy http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0004145 GCST008553 Genome-wide genotyping array 2019-09-02 31220337 Carr DF 2019-06-20 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/31220337 Genome-wide association study of statin-induced myopathy in patients recruited using the UK clinical practice research datalink. Statin-induced myopathy 128 European ancestry cases, 2,501 controls NA Illumina [654642] (imputed) 2 response to statin, myopathy http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0004145 GCST008552 Genome-wide genotyping array 2021-02-08 31366177 Prasad G 2019-07-30 Biomolecules www.ncbi.nlm.nih.gov/pubmed/31366177 Genome-Wide Association Study of Metabolic Syndrome Reveals Primary Genetic Variants at CETP Locus in Indians. Metabolic syndrome 1,596 Indo-European ancestry cases, 562 Indo-European ancestry controls 5,021 Indo-European ancestry cases, 2,914 Indo-European ancestry controls Illumina [519607] 0 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST011098 Genome-wide genotyping array 2019-11-15 31361301 Weingarten MFJ 2019-07-30 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/31361301 Circulating oxytocin is genetically determined and associated with obesity and impaired glucose tolerance. Serum oxytocin levels 951 Sorbian ancestry individuals NA Affymetrix [NR] (imputed) 1 oxytocin measurement http://www.ebi.ac.uk/efo/EFO_0010245 GCST009027 Genome-wide genotyping array 2020-06-26 32558485 Ellinghaus D 2020-06-17 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/32558485 Genomewide Association Study of Severe Covid-19 with Respiratory Failure. Severe COVID-19 infection with respiratory failure (analysis I) 1,610 European ancestry cases, 2,205 European ancestry controls NA Illumina [8582968] (imputed) 23 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90000255 Genome-wide genotyping array 2020-06-26 32558485 Ellinghaus D 2020-06-17 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/32558485 Genomewide Association Study of Severe Covid-19 with Respiratory Failure. Severe COVID-19 infection with respiratory failure (analysis II) 1,610 European ancestry cases, 2,180 European ancestry controls NA Illumina [8582560] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90000256 Genome-wide genotyping array 2021-02-09 33113361 Iacoangeli A 2020-10-01 Cell Rep www.ncbi.nlm.nih.gov/pubmed/33113361 Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics. Amyotrophic lateral sclerosis 22,040 cases, 62,644 controls 837 European ancestry cases, 665 European ancestry controls NR [5356204] 0 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST90013429 Genome-wide genotyping array 2021-07-12 33436679 Chou YC 2021-01-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33436679 Integration of genome-wide association study and expression quantitative trait locus mapping for identification of endometriosis-associated genes. Endometriosis 126 Taiwanese ancestry cases, 96 Taiwanese ancestry controls 133 Taiwanese ancestry cases, 75 Taiwanese ancestry controls Affymetrix [4566885] (imputed) 2 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST012024 Genome-wide genotyping array 2020-04-23 31001917 Grant DJ 2019-04-18 Cancer Med www.ncbi.nlm.nih.gov/pubmed/31001917 Evaluation of vitamin D biosynthesis and pathway target genes reveals UGT2A1/2 and EGFR polymorphisms associated with epithelial ovarian cancer in African American Women. Epithelial ovarian cancer 755 African American cases, 1,235 African American controls NA Illumina [471780] 1 malignant epithelial tumor of ovary http://purl.obolibrary.org/obo/MONDO_0018364 GCST009896 Targeted genotyping array [Oncoarray] 2021-08-13 33632709 Huyghe JR 2021-02-25 Gut www.ncbi.nlm.nih.gov/pubmed/33632709 Genetic architectures of proximal and distal colorectal cancer are partly distinct. Distal/Left-sided colorectal cancer 30,588 European ancestry cases, 64,159 European ancestry controls NA Affymetrix, Illumina [11947015] (imputed) 6 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012202 Genome-wide genotyping array 2021-08-13 33632709 Huyghe JR 2021-02-25 Gut www.ncbi.nlm.nih.gov/pubmed/33632709 Genetic architectures of proximal and distal colorectal cancer are partly distinct. Proximal colorectal cancer 15,706 European ancestry cases, 64,159 European ancestry controls NA Affymetrix, Illumina [11437803] (imputed) 4 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012206 Genome-wide genotyping array 2021-08-13 33632709 Huyghe JR 2021-02-25 Gut www.ncbi.nlm.nih.gov/pubmed/33632709 Genetic architectures of proximal and distal colorectal cancer are partly distinct. Distal colorectal cancer 14,376 European ancestry cases, 64,159 European ancestry controls NA Affymetrix, Illumina [11353757] (imputed) 7 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012205 Genome-wide genotyping array 2021-08-13 33632709 Huyghe JR 2021-02-25 Gut www.ncbi.nlm.nih.gov/pubmed/33632709 Genetic architectures of proximal and distal colorectal cancer are partly distinct. Rectal cancer 16,212 European ancestry cases, 64,159 European ancestry controls NA Affymetrix, Illumina [11358342] (imputed) 3 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST012204 Genome-wide genotyping array 2021-08-13 33632709 Huyghe JR 2021-02-25 Gut www.ncbi.nlm.nih.gov/pubmed/33632709 Genetic architectures of proximal and distal colorectal cancer are partly distinct. Colon cancer 32,002 European ancestry cases, 64,159 European ancestry controls NA Affymetrix, Illumina [11928745] (imputed) 3 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST012203 Genome-wide genotyping array 2020-04-20 30642433 Timmers PR 2019-01-15 Elife www.ncbi.nlm.nih.gov/pubmed/30642433 Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances. Parental lifespan at least 500,193 European ancestry offspring NA NR [up to 9000000] (imputed) 16 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST009890 Genome-wide genotyping array 2020-08-25 32427856 Ahmad S 2020-05-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32427856 CDH6 and HAGH protein levels in plasma associate with Alzheimer's disease in APOE ε4 carriers. HAGH protein levels in plasma 281 individuals NA Illumina [NR] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST010458 Genome-wide genotyping array 2020-08-25 32427856 Ahmad S 2020-05-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32427856 CDH6 and HAGH protein levels in plasma associate with Alzheimer's disease in APOE ε4 carriers. CDH6 protein levels in plasma 281 individuals NA Illumina [NR] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST010459 Genome-wide genotyping array 2020-07-06 32499647 Spracklen CN 2020-05-06 Nature www.ncbi.nlm.nih.gov/pubmed/32499647 Identification of type 2 diabetes loci in 433,540 East Asian individuals. Type 2 diabetes 77,418 East Asian cases, 356,122 East Asian controls NA Affymetrix, Illumina [11800000] (imputed) 183 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST010118 Genome-wide genotyping array 2020-09-16 32573913 Sherva R 2020-06-23 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/32573913 Genome-wide association study of rate of cognitive decline in Alzheimer's disease patients identifies novel genes and pathways. Rate of cognitive decline in Alzheimer's disease 3,946 European ancestry cases NA NR [NR] (imputed) 184 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST010567 Genome-wide genotyping array 2021-02-24 32682390 Wang W 2020-07-18 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/32682390 Heritability and genome-wide association analyses of fasting plasma glucose in Chinese adult twins. Fasting plasma glucose 382 Chinese ancestry twin pairs NA NR [7405822] (imputed) 17 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST011154 Genome-wide genotyping array 2020-09-10 32503578 Yang DW 2020-06-05 J Transl Med www.ncbi.nlm.nih.gov/pubmed/32503578 Genome-wide association study identifies genetic susceptibility loci and pathways of radiation-induced acute oral mucositis. Response to radiotherapy in nasopharyngeal carcinoma (acute oral mucositis) 349 East Asian ancestry cases, 1,118 East Asian ancestry treated controls NA Illumina [3968928] (imputed) 5 oral mucositis, response to radiation http://www.ebi.ac.uk/efo/EFO_1001904, http://purl.obolibrary.org/obo/GO_0009314 GCST010511 Genome-wide genotyping array 2021-02-08 33239696 Steinthorsdottir V 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239696 Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Preeclampsia (fetal genotype effect) 2,145 Central Asian ancestry cases, 2,027 Central Asian ancestry controls, 4,630 European ancestry cases, 373,345 European ancestry controls 452 Kazakh ancestry cases, 361 Kazakh ancestry controls, 580 European ancestry cases, 760 European ancestry controls Illumina [12130433] (imputed) 4 preeclampsia, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0007959 GCST90013475 Genome-wide genotyping array 2021-02-08 33239696 Steinthorsdottir V 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239696 Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Preeclampsia (fetal genotype effect) 2,145 Central Asian ancestry cases, 2,027 Central Asian ancestry controls 452 Kazakh ancestry cases, 361 Kazakh ancestry controls Illumina [at least 12130433] (imputed) 0 preeclampsia, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0007959 GCST90013476 Genome-wide genotyping array 2021-02-08 33239696 Steinthorsdottir V 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239696 Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Preeclampsia (fetal genotype effect) 4,630 European ancestry cases, 373,345 European ancestry controls 580 European ancestry cases, 760 European ancestry controls Illumina [at least 12130433] (imputed) 0 preeclampsia, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0007959 GCST90013477 Genome-wide genotyping array 2021-02-08 33239696 Steinthorsdottir V 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239696 Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Preeclampsia (maternal genotype effect) 2,296 Central Asian ancestry cases, 2,059 Central Asian ancestry controls, 7,219 European ancestry cases, 155,660 European ancestry controls 592 Kazakh ancestry cases, 361 Kazakh ancestry controls, 2,043 European ancestry cases, 6,018 European ancestry controls Illumina [11796347] (imputed) 12 preeclampsia, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90013478 Genome-wide genotyping array 2021-02-08 33239696 Steinthorsdottir V 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239696 Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Preeclampsia (maternal genotype effect) 2,296 Central Asian ancestry cases, 2,059 Central Asian ancestry controls 592 Kazakh ancestry cases, 361 Kazakh ancestry controls Illumina [at least 11796347] (imputed) 0 preeclampsia, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90013479 Genome-wide genotyping array 2021-02-08 33239696 Steinthorsdottir V 2020-11-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33239696 Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women. Preeclampsia (maternal genotype effect) 7,219 European ancestry cases, 155,660 European ancestry controls 2,043 European ancestry cases, 6,018 European ancestry controls Illumina [at least 11796347] (imputed) 0 preeclampsia, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90013480 Genome-wide genotyping array 2021-02-26 33430853 Ustinova M 2021-01-11 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33430853 Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia. Diabetic neuropathy in type 2 diabetes 218 European ancestry cases, 382 European ancestry controls NA Illumina [5378539] (imputed) 2 diabetic neuropathy http://www.ebi.ac.uk/efo/EFO_1000783 GCST011163 Genome-wide genotyping array 2021-02-26 33430853 Ustinova M 2021-01-11 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33430853 Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia. Type 2 diabetes nephropathy 517 European ancestry cases, 84 European ancestry controls NA Illumina [5378539] (imputed) 0 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST011162 Genome-wide genotyping array 2021-02-26 33430853 Ustinova M 2021-01-11 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33430853 Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia. Macrovascular complications in type 2 diabetes 333 European ancestry cases, 226 European ancestry controls NA Illumina [5378539] (imputed) 7 macrovascular complications of diabetes http://www.ebi.ac.uk/efo/EFO_0010977 GCST011161 Genome-wide genotyping array 2021-02-26 33430853 Ustinova M 2021-01-11 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33430853 Novel susceptibility loci identified in a genome-wide association study of type 2 diabetes complications in population of Latvia. Ophthalmic complications in type 2 diabetes 203 European ancestry cases, 398 European ancestry controls NA Illumina [5378539] (imputed) 1 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST011160 Genome-wide genotyping array 2021-05-07 33426524 Ramanan VK 2020-09-26 Brain Commun www.ncbi.nlm.nih.gov/pubmed/33426524 Variants in PPP2R2B and IGF2BP3 are associated with higher tau deposition. Tau burden 754 European ancestry individuals NA Illumina [6417232] (imputed) 12 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST011624 Genome-wide genotyping array 2020-04-17 32128391 Klaric L 2020-02-19 Sci Adv www.ncbi.nlm.nih.gov/pubmed/32128391 Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases. IgG N-glycosylation phenotypes (multivariate analysis) 8,090 European ancestry individuals 2,388 European ancestry individuals Illumina [up to 741151] (imputed) 11 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST009860 Genome-wide genotyping array 2021-05-19 32699239 Jian X 2020-07-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32699239 Genome-wide association study of cognitive function in diverse Hispanics/Latinos: results from the Hispanic Community Health Study/Study of Latinos. Cognitive function 7,606 Hispanic individuals 43,875 European ancestry individuals, 10,399 African American individuals, 3,773 Hispanic individuals Illumina [20000000] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST011695 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Autism spectrum disorder (MTAG) 60,817 individuals NA NR [520857] 10 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST010643 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Depressive symptoms (MTAG) 955,012 individuals NA NR [520857] 63 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST010642 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Bipolar disorder (MTAG) 65,682 individuals NA NR [520857] 63 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST010641 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Schizophrenia (MTAG) 67,764 individuals NA NR [8377093] 110 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST010640 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Attention deficit hyperactivity disorder 55,374 individuals NA NR [8028859] 15 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010649 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Attention deficit hyperactivity disorder (MTAG) 61,421 individuals NA NR [520857] 21 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST010644 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Autism spectrum disorder 46,350 individuals NA NR [9087710] 3 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST010648 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Depressive symptoms 688,809 individuals NA NR [11140414] 49 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST010647 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Bipolar disorder 41,653 individuals NA NR [8956949] 8 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST010646 Genome-wide genotyping array 2020-10-07 32606422 Wu Y 2020-06-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32606422 Multi-trait analysis for genome-wide association study of five psychiatric disorders. Schizophrenia (MTAG) 65,967 individuals NA NR [8377093] 87 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST010645 Genome-wide genotyping array 2020-07-24 32439900 Ntalla I 2020-05-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32439900 Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. PR interval 271,570 European ancestry individuals NA Affymetrix, Illumina [at least 167995] (imputed) 150 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST010320 Genome-wide genotyping array 2020-07-24 32439900 Ntalla I 2020-05-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32439900 Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction. PR interval 271,570 European ancestry individuals, 8,173 African American individuals, 12,823 Hispanic/Latino individuals NA Affymetrix, Illumina [at least 167995] (imputed) 215 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST010321 Genome-wide genotyping array 2020-08-18 32247823 Parisinos CA 2020-04-02 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32247823 Genome-wide and Mendelian randomisation studies of liver MRI yield insights into the pathogenesis of steatohepatitis. Liver fat content (MRI proton density fat fraction measure) 14,440 European ancestry individuals NA Affymetrix [~ 12000000] (imputed) 4 liver fat measurement, liver disease biomarker http://www.ebi.ac.uk/efo/EFO_0010821, http://www.ebi.ac.uk/efo/EFO_0006845 GCST010417 Genome-wide genotyping array 2020-08-18 32247823 Parisinos CA 2020-04-02 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32247823 Genome-wide and Mendelian randomisation studies of liver MRI yield insights into the pathogenesis of steatohepatitis. Liver fibrosis and steatohepatitis severity (MRI cT1 measure) 14,440 European ancestry individuals NA Affymetrix [~ 12000000] (imputed) 7 liver fat measurement, liver disease biomarker http://www.ebi.ac.uk/efo/EFO_0010821, http://www.ebi.ac.uk/efo/EFO_0006845 GCST010418 Genome-wide genotyping array 2021-02-24 32701715 Zhang Y 2020-07-21 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/32701715 PPARGC1B Is Associated with Nontraumatic Osteonecrosis of the Femoral Head: A Genomewide Association Study on a Chart-Reviewed Cohort. Nontraumatic osteonecrosis of the femoral head 118 European ancestry cases, 56,811 European ancestry controls NA Illumina [3905175] (imputed) 24 idiopathic osteonecrosis of the femoral head http://www.ebi.ac.uk/efo/EFO_1001930 GCST011155 Genome-wide genotyping array 2020-06-24 32499645 Thaventhiran JED 2020-05-06 Nature www.ncbi.nlm.nih.gov/pubmed/32499645 Whole-genome sequencing of a sporadic primary immunodeficiency cohort. Antibody-deficiency-associated primary immunodeficiency 733 European, African, Asian and other ancestry cases, 9,225 European, African, Asian and other ancestry controls NA NR [8706207] 0 inborn error of immunity http://purl.obolibrary.org/obo/MONDO_0003778 GCST90000530 Genome-wide sequencing 2020-06-23 24531328 Kozlitina J 2014-02-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24531328 Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease. Nonalcoholic fatty liver disease 2,448 African American individuals, 1,365 European ancestry individuals, 753 Hispanic individuals, 141 other ancestries individuals NA Illumina [138374] 2 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST010096 Exome genotyping array [Exome array] 2021-02-25 32700739 Salinas YD 2020-07-23 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/32700739 Discovery and Mediation Analysis of Cross-Phenotype Associations With Asthma and Body Mass Index in 12q13.2. Asthma 35,373 British ancestry cases, 270,572 British ancestry controls NA Affymetrix [528797] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST011157 Genome-wide genotyping array 2021-02-25 32700739 Salinas YD 2020-07-23 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/32700739 Discovery and Mediation Analysis of Cross-Phenotype Associations With Asthma and Body Mass Index in 12q13.2. Body mass index 305,945 British ancestry individuals NA Affymetrix [528797] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST011156 Genome-wide genotyping array 2021-01-26 31668963 Bay CP 2019-09-27 J Clin Densitom www.ncbi.nlm.nih.gov/pubmed/31668963 Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study. Hip bone mineral content accrual during adolescent growth spurt 125 women, 133 men NA Illumina [509842] 5 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST010986 Genome-wide genotyping array 2021-01-26 31668963 Bay CP 2019-09-27 J Clin Densitom www.ncbi.nlm.nih.gov/pubmed/31668963 Genome-Wide Association Analysis of Longitudinal Bone Mineral Content Data From the Iowa Bone Development Study. Peak hip bone mineral content 190 women, 174 men NA Illumina [509842] 7 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST010987 Genome-wide genotyping array 2020-06-24 32424353 Zhang H 2020-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32424353 Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses. Breast cancer 133,384 European ancestry cases, 113,789 European ancestry controls NA Illumina [~ 10800000] (imputed) 29 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010098 Genome-wide genotyping array 2020-06-24 32424353 Zhang H 2020-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32424353 Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses. Invasive breast cancer 106,278 European ancestry cases, 91,477 European ancestry controls NA Illumina [~ 9700000] (imputed) 22 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010099 Genome-wide genotyping array 2020-06-24 32424353 Zhang H 2020-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32424353 Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses. Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) 8,602 European ancestry triple negative cases, 9,414 European ancestry BRCA1 mutation carrier cases, 100,971 European ancestry controls NA Illumina [~ 9700000] (imputed) 3 triple-negative breast cancer http://www.ebi.ac.uk/efo/EFO_0005537 GCST010100 Genome-wide genotyping array 2021-02-28 32699080 Brhane Y 2020-07-22 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/32699080 Genetic determinants of lung cancer prognosis in never smokers: A pooled analysis in the International Lung Cancer Consortium. Lung cancer (survival time) in never smokers 1,569 European ancestry individuals 887 Japanese ancestry individuals Illumina [629283] (imputed) 4 lung carcinoma, survival time http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0000714 GCST011178 Genome-wide genotyping array 2021-02-28 32699080 Brhane Y 2020-07-22 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/32699080 Genetic determinants of lung cancer prognosis in never smokers: A pooled analysis in the International Lung Cancer Consortium. Lung adenocarcinoma (survival time) in never smokers 1,065 European ancestry individuals 871 Japanese ancestry individuals Illumina [629283] (imputed) 8 survival time, lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000571 GCST011177 Genome-wide genotyping array 2021-03-25 32701512 Cairns J 2020-07-23 JCI Insight www.ncbi.nlm.nih.gov/pubmed/32701512 Pharmacogenomics of aromatase inhibitors in postmenopausal breast cancer and additional mechanisms of anastrozole action. Estrogen level change in anastrozole-treated breast cancer 624 individuals NA Illumina [up to 8000000] (imputed) 5 estrogen measurement, response to aromatase inhibitor http://www.ebi.ac.uk/efo/EFO_0011007, http://purl.obolibrary.org/obo/GO_0061477 GCST011407 Genome-wide genotyping array 2021-01-21 33106546 Johnson TA 2020-10-26 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33106546 Association of an IGHV3-66 gene variant with Kawasaki disease. Kawasaki disease 1,276 East Asian ancestry cases, 5,086 East Asian ancestry controls 2,152 East Asian ancestry cases, 2,751 East Asian ancestry controls Affymetrix, Illumina [6265045] (imputed) 15 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST010979 Genome-wide genotyping array 2019-09-13 28067910 Luo Y 2017-01-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28067910 Exploring the genetic architecture of inflammatory bowel disease by whole-genome sequencing identifies association at ADCY7. Ulcerative colitis 7,760 European ancestry cases, 16,065 European ancestry controls 5,054 European ancestry cases, 450 cases, 162,024 European ancestry controls, 3,905 controls Affymetrix, Illumina [~ 12000000] (imputed) 1 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST008658 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 4-Acetamidobutyric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 4-Acetamidobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021565 GCST90129080 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 4-Guanidinobutyric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 4-Guanidinobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021566 GCST90129081 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 4-Hydroxybenzaldehyde levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 4-Hydroxybenzaldehyde measurement http://www.ebi.ac.uk/efo/EFO_0021567 GCST90129082 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 4-Nitrophenol levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 4-Nitrophenol measurement http://www.ebi.ac.uk/efo/EFO_0021568 GCST90129083 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 4-Pyridoxic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 4-Pyridoxic acid measurement http://www.ebi.ac.uk/efo/EFO_0021569 GCST90129084 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 5-Methyluridine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 5-Methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0021570 GCST90129085 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 5-oxoproline levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90129086 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 5'-Deoxy-5'-(methylthio) adenosine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 5'-Deoxy-5'-(methylthio) adenosine measurement http://www.ebi.ac.uk/efo/EFO_0021571 GCST90129087 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 9,10-dihome levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90129088 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Adenine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Adenine measurement http://www.ebi.ac.uk/efo/EFO_0021573 GCST90129089 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Adenosine 5'-monophosphate levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Adenosine 5'-monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0021574 GCST90129090 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Adipic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Adipic acid measurement http://www.ebi.ac.uk/efo/EFO_0021575 GCST90129091 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Allantoin levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90129092 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Asp-phe levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Asp-phe measurement http://www.ebi.ac.uk/efo/EFO_0021576 GCST90129093 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Azelaic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Azelaic acid measurement http://www.ebi.ac.uk/efo/EFO_0021577 GCST90129094 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Caffeic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Caffeic acid measurement http://www.ebi.ac.uk/efo/EFO_0021578 GCST90129095 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Choline levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90129096 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Cis-5,8,11,14,17-eicosapentaenoic acid (C20:5n3) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 eicosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007760 GCST90129097 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Creatine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90129098 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Creatinine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90129099 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Cyclic AMP levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Cyclic AMP measurement http://www.ebi.ac.uk/efo/EFO_0021580 GCST90129100 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-2-Aminobutyric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-2-Aminobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021581 GCST90129101 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Arabinose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Arabinose measurement http://www.ebi.ac.uk/efo/EFO_0021582 GCST90129102 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Erythronolactone levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Erythronolactone measurement http://www.ebi.ac.uk/efo/EFO_0021583 GCST90129103 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Fructose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Fructose measurement http://www.ebi.ac.uk/efo/EFO_0021584 GCST90129104 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Glucopyranose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Glucopyranose measurement http://www.ebi.ac.uk/efo/EFO_0021585 GCST90129105 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Glucose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Glucose measurement http://www.ebi.ac.uk/efo/EFO_0021586 GCST90129106 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Lactic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Lactic acid measurement http://www.ebi.ac.uk/efo/EFO_0021587 GCST90129107 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Malic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Malic acid measurement http://www.ebi.ac.uk/efo/EFO_0021588 GCST90129108 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Mannose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Mannose measurement http://www.ebi.ac.uk/efo/EFO_0021589 GCST90129109 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Sorbitol levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0021590 GCST90129110 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Sucrose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Sucrose measurement http://www.ebi.ac.uk/efo/EFO_0021591 GCST90129111 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Trehalose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 D-Trehalose measurement http://www.ebi.ac.uk/efo/EFO_0021592 GCST90129112 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Deoxycholic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Deoxycholic acid measurement http://www.ebi.ac.uk/efo/EFO_0021593 GCST90129113 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Dl-2-Aminooctanoic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 X-12510--2-aminooctanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0021313 GCST90129114 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. DL-P-hydroxyphenyllactic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 DL-P-hydroxyphenyllactic acid measurement http://www.ebi.ac.uk/efo/EFO_0021594 GCST90129115 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Dodecanedioic aicd levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Dodecanedioic aicd measurement http://www.ebi.ac.uk/efo/EFO_0021595 GCST90129116 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Dulcitol levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Dulcitol measurement http://www.ebi.ac.uk/efo/EFO_0021596 GCST90129117 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Eudesmic acid (3,4,5-trimethoxybenzoic acid) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 2 Eudesmic acid (3,4,5-trimethoxybenzoic acid) measurement http://www.ebi.ac.uk/efo/EFO_0021597 GCST90129118 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Gluconic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Gluconic acid measurement http://www.ebi.ac.uk/efo/EFO_0021598 GCST90129119 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Glycochenodeoxycholic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Glycochenodeoxycholic acid measurement http://www.ebi.ac.uk/efo/EFO_0021599 GCST90129120 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Glycocholic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 glycocholic acid measurement http://www.ebi.ac.uk/efo/EFO_0010492 GCST90129121 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Glycoursodeoxycholic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Glycoursodeoxycholic acid measurement http://www.ebi.ac.uk/efo/EFO_0021600 GCST90129122 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Hexanoyl glycine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Hexanoyl glycine measurement http://www.ebi.ac.uk/efo/EFO_0021601 GCST90129123 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Hippuric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 hippuric acid measurement http://www.ebi.ac.uk/efo/EFO_0010496 GCST90129124 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Homovanillic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Homovanillic acid measurement http://www.ebi.ac.uk/efo/EFO_0021602 GCST90129125 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Hydrocinnamic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Hydrocinnamic acid measurement http://www.ebi.ac.uk/efo/EFO_0021603 GCST90129126 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Hypoxanthine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90129127 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Indole-5-carboxylic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Indole-5-carboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0021605 GCST90129128 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Inosine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90129129 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Myoinositol levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Myoinositol measurement http://www.ebi.ac.uk/efo/EFO_0021652 GCST90129180 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. N-acetyl-l-leucine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 N-acetyl-l-leucine measurement http://www.ebi.ac.uk/efo/EFO_0021653 GCST90129181 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. N-Acetyl-L-tyrosine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 N-Acetyl-L-tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021654 GCST90129182 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. N-acetylglycine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90129183 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. N,N-Dimethylglycine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 N,N-Dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021655 GCST90129184 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. N6-Acetyl-L-lysine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 N6-Acetyl-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0021656 GCST90129185 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. N6-Succinyl adenosine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 N6-Succinyl adenosine measurement http://www.ebi.ac.uk/efo/EFO_0021657 GCST90129186 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. p-Hydroxyphenyl acetic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 p-Hydroxyphenyl acetic acid measurement http://www.ebi.ac.uk/efo/EFO_0021658 GCST90129187 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Palmitaldehyde levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Palmitaldehyde measurement http://www.ebi.ac.uk/efo/EFO_0021659 GCST90129188 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Palmitic acid / Hexadecanoic acid (C16:0) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Palmitic acid measurement http://www.ebi.ac.uk/efo/EFO_0021660 GCST90129189 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Palmitoleic acid (C16:1) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 palmitoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0007973 GCST90129190 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Pantothenate levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90129191 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Phenylacetyl-L-glutamine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Phenylacetyl-L-glutamine measurement http://www.ebi.ac.uk/efo/EFO_0021661 GCST90129192 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Phenyllactate (PLA) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90129193 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Phenylpyruvic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Phenylpyruvic acid measurement http://www.ebi.ac.uk/efo/EFO_0021663 GCST90129194 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Pipecolinic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Pipecolinic acid measurement http://www.ebi.ac.uk/efo/EFO_0021664 GCST90129195 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Riboflavin levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Riboflavin measurement http://www.ebi.ac.uk/efo/EFO_0021665 GCST90129196 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. S-(5-Adenosy)-L-homocysteine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 S-(5-Adenosy)-L-homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0021666 GCST90129197 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. S-Sulfo-L-cysteine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 S-Sulfo-L-cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021667 GCST90129198 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Sarcosine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90129199 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Suberic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 suberic acid measurement http://www.ebi.ac.uk/efo/EFO_0010534 GCST90129200 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Succinic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Succinic acid measurement http://www.ebi.ac.uk/efo/EFO_0021669 GCST90129201 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Taurochenodesoxycholic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Taurochenodesoxycholic acid measurement http://www.ebi.ac.uk/efo/EFO_0021670 GCST90129202 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Taurocholic acid sodium salt hydrate levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Taurocholic acid sodium salt hydrate measurement http://www.ebi.ac.uk/efo/EFO_0021671 GCST90129203 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Tauroursodeoxycholic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Tauroursodeoxycholic acid measurement http://www.ebi.ac.uk/efo/EFO_0021672 GCST90129204 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Inositol levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 inositol measurement http://www.ebi.ac.uk/efo/EFO_0010504 GCST90129130 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Isonicotinamide levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Isonicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021607 GCST90129131 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Kynurenic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 kynurenic acid measurement http://www.ebi.ac.uk/efo/EFO_0010506 GCST90129132 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Kynurenine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90129133 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-2-Aminobutyric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-2-Aminobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021608 GCST90129134 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-3-Phenyllactic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-3-Phenyllactic acid measurement http://www.ebi.ac.uk/efo/EFO_0021609 GCST90129135 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Arginine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-arginine measurement http://www.ebi.ac.uk/efo/EFO_0006524 GCST90129136 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Asparagine anhydrous levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Asparagine anhydrous measurement http://www.ebi.ac.uk/efo/EFO_0021610 GCST90129137 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Aspartic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Aspartic acid measurement http://www.ebi.ac.uk/efo/EFO_0021611 GCST90129138 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Carnitine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Carnitine measurement http://www.ebi.ac.uk/efo/EFO_0021612 GCST90129139 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Citrulline levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Citrulline measurement http://www.ebi.ac.uk/efo/EFO_0021613 GCST90129140 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Cysteine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021614 GCST90129141 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Cystine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Cystine measurement http://www.ebi.ac.uk/efo/EFO_0021615 GCST90129142 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Glutamic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Glutamic acid measurement http://www.ebi.ac.uk/efo/EFO_0021616 GCST90129143 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Glutamine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Glutamine measurement http://www.ebi.ac.uk/efo/EFO_0021617 GCST90129144 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Histidine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Histidine measurement http://www.ebi.ac.uk/efo/EFO_0021618 GCST90129145 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Isoleucine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021619 GCST90129146 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Leucine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Leucine measurement http://www.ebi.ac.uk/efo/EFO_0021620 GCST90129147 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Lysine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Lysine measurement http://www.ebi.ac.uk/efo/EFO_0021621 GCST90129148 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Malic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Malic acid measurement http://www.ebi.ac.uk/efo/EFO_0021622 GCST90129149 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Methionine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Methionine measurement http://www.ebi.ac.uk/efo/EFO_0021623 GCST90129150 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Ornithine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Ornithine measurement http://www.ebi.ac.uk/efo/EFO_0021624 GCST90129151 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Phenylalanine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021625 GCST90129152 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Pipecolic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Pipecolic acid measurement http://www.ebi.ac.uk/efo/EFO_0021626 GCST90129153 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Proline levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Proline measurement http://www.ebi.ac.uk/efo/EFO_0021627 GCST90129154 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Pyroglutamic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Pyroglutamic acid measurement http://www.ebi.ac.uk/efo/EFO_0021628 GCST90129155 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Saccharopine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Saccharopine measurement http://www.ebi.ac.uk/efo/EFO_0021629 GCST90129156 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Serine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Serine measurement http://www.ebi.ac.uk/efo/EFO_0021630 GCST90129157 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Threonine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Threonine measurement http://www.ebi.ac.uk/efo/EFO_0021631 GCST90129158 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Thyroxine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0021632 GCST90129159 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Tryptophan levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021633 GCST90129160 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Tyrosine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021634 GCST90129161 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Valine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 L-Valine measurement http://www.ebi.ac.uk/efo/EFO_0021635 GCST90129162 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Lauric acid / Dodecanoic acid (C12:0) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Lauric acid measurement http://www.ebi.ac.uk/efo/EFO_0021636 GCST90129163 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Linoleic acid (C18:2n6c) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90129164 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPA 16:0 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPA 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021637 GCST90129165 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 14:0 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021638 GCST90129166 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 16:0 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021639 GCST90129167 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 16:1 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0021640 GCST90129168 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 18:0 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021641 GCST90129169 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 18:1 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0021642 GCST90129170 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 20:0 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021643 GCST90129171 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 20:1 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021644 GCST90129172 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPC 20:2 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPC 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021645 GCST90129173 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPE 14:0 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPE 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021646 GCST90129174 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPE 16:0 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPE 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021647 GCST90129175 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. LysoPE 18:1 levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 LysoPE 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0021648 GCST90129176 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Maltose levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Maltose measurement http://www.ebi.ac.uk/efo/EFO_0021649 GCST90129177 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Methionine sulfoxide levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90129178 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Methylmalonic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Methylmalonic acid measurement http://www.ebi.ac.uk/efo/EFO_0021651 GCST90129179 Genome-wide genotyping array 2020-11-05 33057200 Bao EL 2020-10-14 Nature www.ncbi.nlm.nih.gov/pubmed/33057200 Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells. Myeloproliferative neoplasms 1,086 British ancestry cases, 407,155 British ancestry controls, 640 Finnish ancestry cases, 176,259 Finnish ancestry controls NA Affymetrix [6845584] (imputed) 17 myeloproliferative disorder http://www.ebi.ac.uk/efo/EFO_0004251 GCST90000032 Genome-wide genotyping array 2021-07-27 33276381 Cheng CF 2020-12-04 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/33276381 Genome-wide and candidate gene association analyses identify a 14-SNPs combination for hypertension in patients with type 2 diabetes. Hypertension in type 2 diabetes 454 Han Chinese ancestry cases, 545 Han Chinese ancestry controls 563 Han Chinese ancestry cases, 359 Han Chinese ancestry controls Affymetrix, Illumina [NR] (imputed) 2 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST012136 Genome-wide genotyping array 2021-04-21 33264229 Rickenbacher M 2020-12-01 J Neurosurg Anesthesiol www.ncbi.nlm.nih.gov/pubmed/33264229 Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical Patients. Postoperative cognitive dysfunction (1 week after surgery) 18 cases, 19 controls NA Illumina [506929] 0 response to surgery, Cognitive impairment http://www.ebi.ac.uk/efo/EFO_0009951, http://purl.obolibrary.org/obo/HP_0100543 GCST011525 Genome-wide genotyping array 2021-04-21 33264229 Rickenbacher M 2020-12-01 J Neurosurg Anesthesiol www.ncbi.nlm.nih.gov/pubmed/33264229 Genome-wide Association Study of Postoperative Cognitive Dysfunction in Older Surgical Patients. Postoperative cognitive dysfunction (3 months after surgery) 12 cases, 25 controls NA Illumina [506929] 0 response to surgery, Cognitive impairment http://www.ebi.ac.uk/efo/EFO_0009951, http://purl.obolibrary.org/obo/HP_0100543 GCST011527 Genome-wide genotyping array 2020-02-19 31856834 Chen Z 2019-12-19 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/31856834 Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13. Hypospadias (moderate to severe) 197 Han Chinese ancestry cases, 933 Han Chinese ancestry controls 255 Han Chinese ancestry cases, 573 Han Chinese ancestry controls Illumina [3015028] (imputed) 1 hypospadias http://www.ebi.ac.uk/efo/EFO_0004209 GCST009672 Genome-wide genotyping array 2019-07-16 31188284 Bae H 2019-06-10 Menopause www.ncbi.nlm.nih.gov/pubmed/31188284 Genetic associations with age of menopause in familial longevity. Age at menopause 7,611 European ancestry individuals 3,082 individuals Illumina [at least 7500000] (imputed) 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST008149 Genome-wide genotyping array 2019-01-18 30531941 Doherty A 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531941 GWAS identifies 14 loci for device-measured physical activity and sleep duration. Sleep duration 91,105 European ancestry individuals NA NR [9926106] (imputed) 27 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST006914 Genome-wide genotyping array 2019-01-18 30531941 Doherty A 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531941 GWAS identifies 14 loci for device-measured physical activity and sleep duration. Sedentary behaviour duration 91,105 European ancestry individuals NA NR [9926106] (imputed) 6 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006913 Genome-wide genotyping array 2019-02-11 30531941 Doherty A 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531941 GWAS identifies 14 loci for device-measured physical activity and sleep duration. Physical activity (walking duration) 91,105 European ancestry individuals NA NR [9926106] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST007110 Genome-wide genotyping array 2019-01-18 30531941 Doherty A 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531941 GWAS identifies 14 loci for device-measured physical activity and sleep duration. Physical activity (moderate intensity activity duration) 91,105 European ancestry individuals NA NR [9926106] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006915 Genome-wide genotyping array 2019-01-18 30531941 Doherty A 2018-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30531941 GWAS identifies 14 loci for device-measured physical activity and sleep duration. Physical activity (overall physical activity time) 91,105 European ancestry individuals NA NR [9926106] (imputed) 7 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST006912 Genome-wide genotyping array 2021-06-23 33321125 Nasu T 2020-12-13 Int J Cardiol www.ncbi.nlm.nih.gov/pubmed/33321125 A genome-wide association study for highly sensitive cardiac troponin T levels identified a novel genetic variation near a RBAK-ZNF890P locus in the Japanese general population. HIgh-sensitivity cardiac troponin T levels (high vs low) 967 Japanese ancestry high hs-cTnT individuals, 2,816 Japanese ancestry low hs-cTnT individuals 190 Japanese ancestry high hs-cTnT individuals, 708 Japanese ancestry low hs-cTnT individuals Illumina [7151284] (imputed) 4 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST011962 Genome-wide genotyping array 2021-06-23 33321125 Nasu T 2020-12-13 Int J Cardiol www.ncbi.nlm.nih.gov/pubmed/33321125 A genome-wide association study for highly sensitive cardiac troponin T levels identified a novel genetic variation near a RBAK-ZNF890P locus in the Japanese general population. High-sensitivity cardiac troponin T levels 3,783 Japanese ancestry individuals 898 Japanese ancestry individuals Illumina [7151284] (imputed) 3 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST011961 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. (S)-(-)-2-Hydroxyisocaproic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 (S)-(-)-2-Hydroxyisocaproic acid measurement http://www.ebi.ac.uk/efo/EFO_0021542 GCST90129055 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 1-Methylhistidine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90129056 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 1-Methylxanthine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90129057 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 1,3-Dimethyluric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 1,3-Dimethyluric acid measurement http://www.ebi.ac.uk/efo/EFO_0021544 GCST90129058 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 1,3,7-trimethyluric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 1,3,7-trimethyluric acid measurement http://www.ebi.ac.uk/efo/EFO_0021545 GCST90129059 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 1,4-dihydro-1-Methyl-4-oxo-3-pyridinecarboxamide levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 1,4-dihydro-1-Methyl-4-oxo-3-pyridinecarboxamide measurement http://www.ebi.ac.uk/efo/EFO_0021546 GCST90129060 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 1,7-Dimethylxanthine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 1,7-Dimethylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021547 GCST90129061 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2-(dimethylamino) guanosine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 2-(dimethylamino) guanosine measurement http://www.ebi.ac.uk/efo/EFO_0021548 GCST90129062 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2-Aminoethanesulfonic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 2-Aminoethanesulfonic acid measurement http://www.ebi.ac.uk/efo/EFO_0021549 GCST90129063 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2-Hydroxybutanoic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 2-Hydroxybutanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0021550 GCST90129064 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2-Hydroxyisocaproic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 2-Hydroxyisocaproic acid measurement http://www.ebi.ac.uk/efo/EFO_0021551 GCST90129065 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2-Methylsuccinic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 2-Methylsuccinic acid measurement http://www.ebi.ac.uk/efo/EFO_0021552 GCST90129066 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2-Picolinic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 2-Picolinic acid measurement http://www.ebi.ac.uk/efo/EFO_0021553 GCST90129067 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2,3-dimethylsuccinic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 2,3-dimethylsuccinic acid measurement http://www.ebi.ac.uk/efo/EFO_0021554 GCST90129068 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 2,6-Diaminooimelic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 2,6-Diaminooimelic acid measurement http://www.ebi.ac.uk/efo/EFO_0021555 GCST90129069 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-(3-hydroxyphenyl) propionate acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3-(3-hydroxyphenyl) propionate acid measurement http://www.ebi.ac.uk/efo/EFO_0021556 GCST90129070 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Hydroxy-3-methyl butyric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3-Hydroxy-3-methyl butyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021557 GCST90129071 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Hydroxybutyrate levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90129072 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Hydroxyhippuric acid (m-Hydroxyhippuricacid) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3-Hydroxyhippuric acid (m-Hydroxyhippuricacid) measurement http://www.ebi.ac.uk/efo/EFO_0021558 GCST90129073 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolebutyric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3-Indolebutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021559 GCST90129074 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 3 3-Indolepropionic acid measurement http://www.ebi.ac.uk/efo/EFO_0021560 GCST90129075 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Methylcrotonyl glycine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3-Methylcrotonyl glycine measurement http://www.ebi.ac.uk/efo/EFO_0021561 GCST90129076 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-N-Methyl-L-histidine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3-N-Methyl-L-histidine measurement http://www.ebi.ac.uk/efo/EFO_0021562 GCST90129077 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3,3',5-Triiodo-L-thyronine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3,3',5-Triiodo-L-thyronine measurement http://www.ebi.ac.uk/efo/EFO_0021563 GCST90129078 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3,4,5-Trimethoxycinnamic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 3,4,5-Trimethoxycinnamic acid measurement http://www.ebi.ac.uk/efo/EFO_0021564 GCST90129079 Genome-wide genotyping array 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Amygdala volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 amygdala volume change measurement http://www.ebi.ac.uk/efo/EFO_0021490 GCST90128543 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Caudate volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 caudate volume change measurement http://www.ebi.ac.uk/efo/EFO_0021491 GCST90128544 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebellum cortex volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebellum cortex volume change measurement http://www.ebi.ac.uk/efo/EFO_0021497 GCST90128545 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebellum white matter volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebellum white matter volume change measurement http://www.ebi.ac.uk/efo/EFO_0021498 GCST90128546 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebral white matter volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 8 cerebral white matter volume change measurement http://www.ebi.ac.uk/efo/EFO_0021499 GCST90128547 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortex volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cortex volume change measurement http://www.ebi.ac.uk/efo/EFO_0021500 GCST90128548 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortical thickness change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cortical thickness change measurement http://www.ebi.ac.uk/efo/EFO_0021501 GCST90128549 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Hippocampus volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 9 hippocampus volume change measurement http://www.ebi.ac.uk/efo/EFO_0021492 GCST90128550 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Lateral ventricle volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 lateral ventricle volume change measurement http://www.ebi.ac.uk/efo/EFO_0021502 GCST90128551 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Nucleus accumbens volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 8 nucleus accumbens volume change measurement http://www.ebi.ac.uk/efo/EFO_0021493 GCST90128552 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Pallidum volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 9 pallidum volume change measurement http://www.ebi.ac.uk/efo/EFO_0021494 GCST90128553 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Putamen volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 putamen volume change measurement http://www.ebi.ac.uk/efo/EFO_0021495 GCST90128554 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Brain surface area change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 8 cortical surface area change measurement http://www.ebi.ac.uk/efo/EFO_0021503 GCST90128555 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Thalamus volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 thalamus volume change measurement http://www.ebi.ac.uk/efo/EFO_0021496 GCST90128556 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Total brain volume change rate 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 total brain volume change measurement http://www.ebi.ac.uk/efo/EFO_0021504 GCST90128557 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Amygdala volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 amygdala volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021490, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128558 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Caudate volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 caudate volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021491, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128559 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebellum cortex volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebellum cortex volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021497, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128560 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebellum white matter volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebellum white matter volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021498, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128561 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebral white matter volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebral white matter volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021499, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128562 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortex volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cortex volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021500, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128563 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortical thickness change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 7 cortical thickness change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021501, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128564 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Hippocampus volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 hippocampus volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021492, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128565 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Lateral ventricle volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 9 age at assessment, lateral ventricle volume change measurement http://www.ebi.ac.uk/efo/EFO_0008007, http://www.ebi.ac.uk/efo/EFO_0021502 GCST90128566 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Nucleus accumbens volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 4 nucleus accumbens volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021493, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128567 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Pallidum volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 pallidum volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021494, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128568 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Putamen volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 putamen volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021495, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128569 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Brain surface area change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cortical surface area change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021503, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128570 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Thalamus volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 9 thalamus volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021496, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128571 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Total brain volume change rate x age interaction (1df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 total brain volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021504, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128572 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Amygdala volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 8 amygdala volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021490, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128573 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Caudate volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 7 caudate volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021491, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128574 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebellum cortex volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebellum cortex volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021497, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128575 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebellum white matter volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebellum white matter volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021498, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128576 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebral white matter volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cerebral white matter volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021499, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128577 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortex volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cortex volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021500, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128578 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortical thickness change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 8 cortical thickness change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021501, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128579 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Hippocampus volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 hippocampus volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021492, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128580 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Lateral ventricle volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 age at assessment, lateral ventricle volume change measurement http://www.ebi.ac.uk/efo/EFO_0008007, http://www.ebi.ac.uk/efo/EFO_0021502 GCST90128581 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Nucleus accumbens volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 9 nucleus accumbens volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021493, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128582 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Pallidum volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 pallidum volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021494, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128583 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Putamen volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 putamen volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021495, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128584 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Brain surface area change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 cortical surface area change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021503, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128585 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Thalamus volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 thalamus volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021496, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128586 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Total brain volume change rate x age interaction (2df) 15,100 European ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 10 total brain volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021504, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128587 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Caudate volume change rate x age interaction (2df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 caudate volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021491, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128588 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cerebellum white matter volume change rate x age interaction (2df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 2 cerebral white matter volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021499, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128589 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortex volume change rate x age interaction (2df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 cortex volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021500, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128590 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Cortical thickness change rate x age interaction (2df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 cortical thickness change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021501, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128591 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Hippocampus volume change rate x age interaction (2df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 hippocampus volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021492, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128592 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Lateral ventricle volume change rate 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 2 lateral ventricle volume change measurement http://www.ebi.ac.uk/efo/EFO_0021502 GCST90128593 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Pallidum volume change rate 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 pallidum volume change measurement http://www.ebi.ac.uk/efo/EFO_0021494 GCST90128594 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Pallidum volume change rate x age interaction (1df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 pallidum volume change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021494, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128595 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Brain surface area change rate x age interaction (1df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 cortical surface area change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021503, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128596 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Brain surface area change rate x age interaction (2df) 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 cortical surface area change measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0021503, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90128597 Genome-wide genotyping array, Genome-wide sequencing 2022-07-14 35383335 Brouwer RM 2022-04-05 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/35383335 Genetic variants associated with longitudinal changes in brain structure across the lifespan. Total brain volume change rate 15,100 European ancestry individuals, 490 Mixed ancestry individuals, 50 South African ancestry individuals NA Affymetrix, Illumina, Perlegen [6200000] (imputed) 1 total brain volume change measurement http://www.ebi.ac.uk/efo/EFO_0021504 GCST90128598 Genome-wide genotyping array, Genome-wide sequencing 2020-10-30 31844061 Malaria Genomic Epidemiology Network 2019-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31844061 Insights into malaria susceptibility using genome-wide data on 17,000 individuals from Africa, Asia and Oceania. Malaria 7,957 African ancestry cases, 7,746 African ancestry controls, 718 Asian ancestry cases, 546 Asian ancestry controls, 402 Oceanian cases, 374 Oceanian controls NR Illumina [1492601] (imputed) 100 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST010725 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Theobromine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90129205 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. trans,trans-Muconic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 trans,trans-Muconic acid measurement http://www.ebi.ac.uk/efo/EFO_0021674 GCST90129206 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Trimethylamine N-oxide levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 plasma trimethylamine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0005691 GCST90129207 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Uric acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90129208 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Uridine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90129209 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Uridine 5-monophosphate levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Uridine 5-monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0021675 GCST90129210 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Urocanic acid levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Urocanic acid (RG) measurement http://www.ebi.ac.uk/efo/EFO_0021676 GCST90129211 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. alpha-Linolenic acid (C18:3n3) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 alpha-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007759 GCST90129212 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. beta-Nicotinamide mononucleotide levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 beta-Nicotinamide mononucleotide measurement http://www.ebi.ac.uk/efo/EFO_0021677 GCST90129213 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. beta-Pseudouridine levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 beta-Pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021678 GCST90129214 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. gamma-Linolenic acid (C18:3n6) levels in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 gamma-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007762 GCST90129215 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Histidine to Uric acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Histidine to Uric acid ratio http://www.ebi.ac.uk/efo/EFO_0021679 GCST90129216 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Cis-5,8,11,14,17-eicosapentaenoic acid (C20:5n3) to LysoPC 20:2 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 0 Cis-5,8,11,14,17-eicosapentaenoic acid (C20:5n3) to LysoPC 20:2 ratio http://www.ebi.ac.uk/efo/EFO_0021680 GCST90129217 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Tryptophan to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Tryptophan to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021681 GCST90129218 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Lysine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Lysine ratio http://www.ebi.ac.uk/efo/EFO_0021682 GCST90129219 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Uridine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Uridine ratio http://www.ebi.ac.uk/efo/EFO_0021683 GCST90129220 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Adenine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Adenine ratio http://www.ebi.ac.uk/efo/EFO_0021684 GCST90129221 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Methionine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Methionine ratio http://www.ebi.ac.uk/efo/EFO_0021685 GCST90129222 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Phenylalanine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Phenylalanine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021686 GCST90129223 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Tyrosine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Tyrosine ratio http://www.ebi.ac.uk/efo/EFO_0021687 GCST90129224 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Phenylpyruvic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Phenylpyruvic acid ratio http://www.ebi.ac.uk/efo/EFO_0021688 GCST90129225 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Ornithine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Ornithine ratio http://www.ebi.ac.uk/efo/EFO_0021689 GCST90129226 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Glutamine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Glutamine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021690 GCST90129227 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Taurocholic acid sodium salt hydrate ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Taurocholic acid sodium salt hydrate ratio http://www.ebi.ac.uk/efo/EFO_0021691 GCST90129228 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Valine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Valine ratio http://www.ebi.ac.uk/efo/EFO_0021692 GCST90129229 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to (S)-(-)-2-Hydroxyisocaproic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to (S)-(-)-2-Hydroxyisocaproic acid ratio http://www.ebi.ac.uk/efo/EFO_0021743 GCST90129280 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Creatinine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Creatinine ratio http://www.ebi.ac.uk/efo/EFO_0021744 GCST90129281 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Pyroglutamic acid to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Pyroglutamic acid to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021745 GCST90129282 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to gamma-Linolenic acid (C18:3n6) ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to gamma-Linolenic acid (C18:3n6) ratio http://www.ebi.ac.uk/efo/EFO_0021746 GCST90129283 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to N,N-Dimethylglycine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to N,N-Dimethylglycine ratio http://www.ebi.ac.uk/efo/EFO_0021747 GCST90129284 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to SubericAcid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to SubericAcid ratio http://www.ebi.ac.uk/efo/EFO_0021748 GCST90129285 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 2-(dimethylamino) guanosine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 2-(dimethylamino) guanosine ratio http://www.ebi.ac.uk/efo/EFO_0021749 GCST90129286 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 14:0 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 14:0 ratio http://www.ebi.ac.uk/efo/EFO_0021750 GCST90129287 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 4-Hydroxybenzaldehyde ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 4-Hydroxybenzaldehyde ratio http://www.ebi.ac.uk/efo/EFO_0021751 GCST90129288 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Azelaic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Azelaic acid ratio http://www.ebi.ac.uk/efo/EFO_0021752 GCST90129289 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to cis-5,8,11,14,17-Eicosapentaenoic acid (C20:5n3) ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to cis-5,8,11,14,17-Eicosapentaenoic acid C20:5n3) ratio http://www.ebi.ac.uk/efo/EFO_0021753 GCST90129290 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Hypoxanthine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Hypoxanthine ratio http://www.ebi.ac.uk/efo/EFO_0021754 GCST90129291 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Proline to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Proline to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021755 GCST90129292 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Trehalose to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 D-Trehalose to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021756 GCST90129293 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Methylmalonic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Methylmalonic acid ratio http://www.ebi.ac.uk/efo/EFO_0021757 GCST90129294 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to alpha-Linolenic acid (C18:3n3) ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to alpha-Linolenic acid (C18:3n3) ratio http://www.ebi.ac.uk/efo/EFO_0021758 GCST90129295 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to S-Sulfo-L-cysteine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to S-Sulfo-L-cysteine ratio http://www.ebi.ac.uk/efo/EFO_0021759 GCST90129296 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 20:0 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 20:0 ratio http://www.ebi.ac.uk/efo/EFO_0021760 GCST90129297 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to beta-Pseudouridine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to beta-Pseudouridine ratio http://www.ebi.ac.uk/efo/EFO_0021761 GCST90129298 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Dulcitol to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Dulcitol to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021762 GCST90129299 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 4-Nitrophenol ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 4-Nitrophenol ratio http://www.ebi.ac.uk/efo/EFO_0021763 GCST90129300 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Indole-5-carboxylic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Indole-5-carboxylic acid ratio http://www.ebi.ac.uk/efo/EFO_0021764 GCST90129301 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Pantothenate to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Pantothenate to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021765 GCST90129302 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Lauric acid/Dodecanoic acid (C12:0) ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Lauric acid ratio http://www.ebi.ac.uk/efo/EFO_0021766 GCST90129303 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Homovanillic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Homovanillic acid ratio http://www.ebi.ac.uk/efo/EFO_0021767 GCST90129304 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Asp-phe to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Asp-phe to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021693 GCST90129230 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Histidine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Histidine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021694 GCST90129231 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 3,3',5-Triiodo-L-thyronine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 3,3',5-Triiodo-L-thyronine ratio http://www.ebi.ac.uk/efo/EFO_0021695 GCST90129232 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Arabinose to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 D-Arabinose to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021696 GCST90129233 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 16:0 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 16:0 ratio http://www.ebi.ac.uk/efo/EFO_0021697 GCST90129234 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Threonine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Threonine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021698 GCST90129235 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 18:1 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 18:1 ratio http://www.ebi.ac.uk/efo/EFO_0021699 GCST90129236 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to N6-Acetyl-L-lysine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to N6-Acetyl-L-lysine ratio http://www.ebi.ac.uk/efo/EFO_0021700 GCST90129237 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Thyroxine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Thyroxine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021701 GCST90129238 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Aspartic acid to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Aspartic acid to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021702 GCST90129239 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Trimethylamine N-oxide ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Trimethylamine N-oxide ratio http://www.ebi.ac.uk/efo/EFO_0021703 GCST90129240 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Uric acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Uric acid ratio http://www.ebi.ac.uk/efo/EFO_0021704 GCST90129241 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to D-Fructose ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to D-Fructose ratio http://www.ebi.ac.uk/efo/EFO_0021705 GCST90129242 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Sarcosine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Sarcosine ratio http://www.ebi.ac.uk/efo/EFO_0021706 GCST90129243 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Choline ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Choline ratio http://www.ebi.ac.uk/efo/EFO_0021707 GCST90129244 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Glutamic acid to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Glutamic acid to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021708 GCST90129245 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Serine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Serine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021709 GCST90129246 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to S-(5-Adenosy) -L-homocysteine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to S-(5-Adenosy) -L-homocysteine ratio http://www.ebi.ac.uk/efo/EFO_0021710 GCST90129247 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to D-2-Aminobutyric acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to D-2-Aminobutyric acid ratio http://www.ebi.ac.uk/efo/EFO_0021711 GCST90129248 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 16:1 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 16:1 ratio http://www.ebi.ac.uk/efo/EFO_0021712 GCST90129249 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Hippuric acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Hippuric acid ratio http://www.ebi.ac.uk/efo/EFO_0021713 GCST90129250 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Pipecolinic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Pipecolinic acid ratio http://www.ebi.ac.uk/efo/EFO_0021714 GCST90129251 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Citrulline to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Citrulline to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021715 GCST90129252 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Saccharopine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Saccharopine ratio http://www.ebi.ac.uk/efo/EFO_0021716 GCST90129253 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 5-oxoproline ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 5-oxoproline ratio http://www.ebi.ac.uk/efo/EFO_0021717 GCST90129254 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Asparagine Anhydrous to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Asparagine Anhydrous to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021718 GCST90129255 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Kinurenine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Kinurenine ratio http://www.ebi.ac.uk/efo/EFO_0021719 GCST90129256 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 18:0 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 18:0 ratio http://www.ebi.ac.uk/efo/EFO_0021720 GCST90129257 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-2-Aminobutyric acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-2-Aminobutyric acid ratio http://www.ebi.ac.uk/efo/EFO_0021721 GCST90129258 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 2-Picolinic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 2-Picolinic acid ratio http://www.ebi.ac.uk/efo/EFO_0021722 GCST90129259 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 2-Methylsuccinic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 2-Methylsuccinic acid ratio http://www.ebi.ac.uk/efo/EFO_0021723 GCST90129260 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 20:2 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 20:2 ratio http://www.ebi.ac.uk/efo/EFO_0021724 GCST90129261 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 4-Guanidinobutyric acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 4-Guanidinobutyric acid ratio http://www.ebi.ac.uk/efo/EFO_0021725 GCST90129262 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Isonicotinamide ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Isonicotinamide ratio http://www.ebi.ac.uk/efo/EFO_0021726 GCST90129263 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 5-Methyluridine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 5-Methyluridine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021727 GCST90129264 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to N-acetylglycine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to N-acetylglycine ratio http://www.ebi.ac.uk/efo/EFO_0021728 GCST90129265 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to N-Acetyl-L-tyrosine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to N-Acetyl-L-tyrosine ratio http://www.ebi.ac.uk/efo/EFO_0021729 GCST90129266 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. L-Cystine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 L-Cystine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021730 GCST90129267 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Cyclic AMP ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Cyclic AMP ratio http://www.ebi.ac.uk/efo/EFO_0021731 GCST90129268 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Carnitine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Carnitine ratio http://www.ebi.ac.uk/efo/EFO_0021732 GCST90129269 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 1,4-dihydro-1-Methyl-4-oxo-3-pyridinecarboxamide ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 1,4-dihydro-1-Methyl-4-oxo-3-pyridinecarboxamide ratio http://www.ebi.ac.uk/efo/EFO_0021733 GCST90129270 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Creatine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Creatine ratio http://www.ebi.ac.uk/efo/EFO_0021734 GCST90129271 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Dodecanedioic aicd ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Dodecanedioic aicd ratio http://www.ebi.ac.uk/efo/EFO_0021735 GCST90129272 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to LysoPC 20:1 ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to LysoPC 20:1 ratio http://www.ebi.ac.uk/efo/EFO_0021736 GCST90129273 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Arginine ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Arginine ratio http://www.ebi.ac.uk/efo/EFO_0021737 GCST90129274 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Kynurenic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Kynurenic acid ratio http://www.ebi.ac.uk/efo/EFO_0021738 GCST90129275 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 2-Hydroxyisocaproic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 2-Hydroxyisocaproic acid ratio http://www.ebi.ac.uk/efo/EFO_0021739 GCST90129276 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 4-Pyridoxic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 4-Pyridoxic acid ratio http://www.ebi.ac.uk/efo/EFO_0021740 GCST90129277 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to L-Pipecolic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to L-Pipecolic acid ratio http://www.ebi.ac.uk/efo/EFO_0021741 GCST90129278 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to 3-Hydroxybutyrate ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to 3-Hydroxybutyrate ratio http://www.ebi.ac.uk/efo/EFO_0021742 GCST90129279 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. N-acetyl-l-leucine to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 N-acetyl-l-leucine to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021768 GCST90129305 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Myoinositol ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Myoinositol ratio http://www.ebi.ac.uk/efo/EFO_0021769 GCST90129306 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Urocanic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Urocanic acid (RG) ratio http://www.ebi.ac.uk/efo/EFO_0021770 GCST90129307 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. Riboflavin to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 Riboflavin to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021771 GCST90129308 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. 3-Indolepropionic acid to Maltose ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 3-Indolepropionic acid to Maltose ratio http://www.ebi.ac.uk/efo/EFO_0021772 GCST90129309 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Malic acid to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 D-Malic acid to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021773 GCST90129310 Genome-wide genotyping array 2022-07-14 33634981 Wang Z 2021-02-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/33634981 Genome-wide association study of metabolites in patients with coronary artery disease identified novel metabolite quantitative trait loci. D-Sucrose to 3-Indolepropionic acid ratio in coronary artery disease 1,551 Han Chinese ancestry individuals NA Illumina [3435396] (imputed) 1 D-Sucrose to 3-Indolepropionic acid ratio http://www.ebi.ac.uk/efo/EFO_0021774 GCST90129311 Genome-wide genotyping array 2021-04-30 33310085 Emdin CA 2020-12-10 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/33310085 Association of genetic variation with cirrhosis: a multi-trait genome-wide association and gene-environment interaction study. Cirrhosis (multi-trait analysis) 4,829 European, African, Asian and unknown ancestry cases, 72,705 European, African, Asian and unknown ancestry controls, 362,539 European, African, Asian and unknown ancestry individuals with ALT measurements 3,554 European, African, Asian and unknown ancestry cases, 343,286 European, African, Asian and unknown ancestry controls Affymetrix, Illumina [3163456] (imputed) 5 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST011586 Genome-wide genotyping array 2019-02-06 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Educational attainment (years of education) approximately 455,000 European ancestry individuals NA NR [~ 8900000] (imputed) 322 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST007037 Genome-wide genotyping array 2019-02-06 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Balding type 1 approximately 208,000 European ancestry individuals NA NR [~ 8900000] (imputed) 348 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST007038 Genome-wide genotyping array 2019-02-06 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Body mass index approximately 458,000 European ancestry individuals NA NR [~ 8900000] (imputed) 964 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST007039 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Heel bone mineral density approximately 446,000 European ancestry individuals NA NR [~ 8900000] (imputed) 1176 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST007066 Genome-wide genotyping array 2019-05-21 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Height approximately 458,000 European ancestry individuals NA NR [~ 8900000] (imputed) 2451 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST007841 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Waist-hip ratio approximately 458,000 European ancestry individuals NA NR [~ 8900000] (imputed) 509 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST007067 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Eosinophil counts approximately 440,000 European ancestry individuals NA NR [~ 8900000] (imputed) 737 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST007065 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Mean corpuscular hemoglobin approximately 443,000 European ancestry individuals NA NR [~ 8900000] (imputed) 799 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST007068 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Red blood cell count approximately 445,000 European ancestry individuals NA NR [~ 8900000] (imputed) 891 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST007069 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Red cell distribution width approximately 445,000 European ancestry individuals NA NR [~ 8900000] (imputed) 690 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST007074 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. White blood cell count approximately 444,000 European ancestry individuals NA NR [~ 8900000] (imputed) 757 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST007070 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Autoimmune traits approximately 459,000 European ancestry individuals NA NR [~ 8900000] (imputed) 85 autoimmune disease http://www.ebi.ac.uk/efo/EFO_0005140 GCST007071 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Cardiovascular disease approximately 459,000 European ancestry individuals NA NR [~ 8900000] (imputed) 316 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST007072 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Eczema approximately 459,000 European ancestry individuals NA NR [~ 8900000] (imputed) 198 Eczema http://purl.obolibrary.org/obo/HP_0000964 GCST007075 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Hypothyroidism approximately 459,000 European ancestry individuals NA NR [~ 8900000] (imputed) 153 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST007073 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Respiratory diseases approximately 459,000 European ancestry individuals NA NR [~ 8900000] (imputed) 109 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST007076 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Type 2 diabetes approximately 459,000 European ancestry individuals NA NR [~ 8900000] (imputed) 85 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007077 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Menarche (age at onset) approximately 242,000 European ancestry individuals NA NR [~ 8900000] (imputed) 340 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST007078 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Age at menopause approximately 143,000 European ancestry individuals NA NR [~ 8900000] (imputed) 93 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST007079 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Lung function (FEV1/FVC) approximately 370,000 European ancestry individuals NA NR [~ 8900000] (imputed) 719 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST007080 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Lung function (FVC) approximately 372,000 European ancestry individuals NA NR [~ 8900000] (imputed) 570 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST007081 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Hair color approximately 452,000 European ancestry individuals NA NR [~ 8900000] (imputed) 449 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST007082 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Morning person approximately 410,000 European ancestry individuals NA NR [~ 8900000] (imputed) 168 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST007083 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Neuroticism approximately 372,000 European ancestry individuals NA NR [~ 8900000] (imputed) 147 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST007084 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Smoking status approximately 458,000 European ancestry individuals NA NR [~ 8900000] (imputed) 181 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST007085 Genome-wide genotyping array 2022-01-05 33332786 Zhang Y 2020-12-15 Spine (Phila Pa 1976) www.ncbi.nlm.nih.gov/pubmed/33332786 Genome-Wide Association Analysis Across 16,956 Patients Identifies a Novel Genetic Association Between BMP6, NIPAL1, CNGA1 and Spondylosis. Spondylosis 4,434 European ancestry cases, 9,416 European ancestry controls NA Illumina [6740241] (imputed) 23 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST012616 Genome-wide genotyping array 2021-06-24 33328473 Ahluwalia TS 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328473 FUT2-ABO epistasis increases the risk of early childhood asthma and Streptococcus pneumoniae respiratory illnesses. Childhood asthma with severe exacerbations 2,866 European ancestry cases, 65,415 European ancestry controls NA Illumina [up to 525976] (imputed) 18 asthma exacerbation measurement http://www.ebi.ac.uk/efo/EFO_0007614 GCST011975 Genome-wide genotyping array 2021-06-18 33308445 Ortiz-Fernandez L 2020-12-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33308445 Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Takayasu arteritis 286 European ancestry cases, 2,652 European ancestry controls, 76 Han Chinese ancestry cases, 889 Han Chinese ancestry controls, 46 South Asian ancestry cases, 501 South Asian ancestry controls, 683 Turkish ancestry cases, 1,721 Turkish ancestry controls NA Illumina [up to 4495750] (imputed) 34 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST011939 Genome-wide genotyping array 2021-06-18 33308445 Ortiz-Fernandez L 2020-12-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33308445 Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Takayasu arteritis 683 Turkish ancestry cases, 1,721 Turkish ancestry controls NA Illumina [4495750] (imputed) 14 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST011938 Genome-wide genotyping array 2021-06-18 33308445 Ortiz-Fernandez L 2020-12-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33308445 Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Takayasu arteritis 229 European ancestry cases, 1,088 European ancestry controls NA Illumina [4388215] (imputed) 9 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST011937 Genome-wide genotyping array 2021-06-18 33308445 Ortiz-Fernandez L 2020-12-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33308445 Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Takayasu arteritis 76 Han Chinese ancestry cases, 889 Han Chinese ancestry controls NA Illumina [3403929] (imputed) 5 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST011936 Genome-wide genotyping array 2021-06-18 33308445 Ortiz-Fernandez L 2020-12-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33308445 Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Takayasu arteritis 46 South Asian ancestry cases, 501 South Asian ancestry controls NA Illumina [3882561] (imputed) 0 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST011935 Genome-wide genotyping array 2021-06-18 33308445 Ortiz-Fernandez L 2020-12-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33308445 Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study. Takayasu arteritis 57 Italian ancestry cases, 931 Italian ancestry controls NA Illumina [4425173] (imputed) 2 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST011934 Genome-wide genotyping array 2019-08-21 31320639 Hillary RF 2019-07-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31320639 Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936. Neurological blood protein biomarker levels 750 European ancestry individuals NA Illumina [8683751] (imputed) 69 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST008478 Genome-wide genotyping array 2019-02-27 30563176 Westermair AL 2018-12-05 Biomolecules www.ncbi.nlm.nih.gov/pubmed/30563176 Association of Genetic Variation at AQP4 Locus with Vascular Depression. Severe depressive disorders in coronary artery disease 78 European ancestry cases, 264 European ancestry controls NA Affymetrix [6341066] (imputed) 5 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST007230 Genome-wide genotyping array 2019-02-27 25108385 Yang SK 2014-08-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25108385 A common missense variant in NUDT15 confers susceptibility to thiopurine-induced leukopenia. Thiopurine-induced early leukopenia in Crohn's disease 33 Korean ancestry cases, 307 Korean ancestry controls 33 Korean ancestry cases, 325 Korean ancestry controls Illumina [531416] (imputed) 1 leukopenia, response to thiopurine http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0006317 GCST007229 Targeted genotyping array [ImmunoChip] 2019-01-21 30326835 Li Z 2018-10-16 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/30326835 Genetic variants in nuclear DNA along with environmental factors modify mitochondrial DNA copy number: a population-based exome-wide association study. Mitochondrial DNA levels 301 Chinese ancestry individuals NA Illumina [238927] 1 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST006936 Exome genotyping array [Exome array] 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Sunburns approximately 344,000 European ancestry individuals NA NR [~ 8900000] (imputed) 84 sunburn http://www.ebi.ac.uk/efo/EFO_0003958 GCST007086 Genome-wide genotyping array 2019-02-08 30595370 Kichaev G 2018-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30595370 Leveraging Polygenic Functional Enrichment to Improve GWAS Power. Systolic blood pressure approximately 422,000 European ancestry individuals NA NR [~ 8900000] (imputed) 720 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST007087 Genome-wide genotyping array 2019-03-27 30718454 Arnau-Soler A 2019-02-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30718454 Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Depressive symptoms 103,976 European ancestry individuals NA Affymetrix, Illumina [1009208] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST007407 Genome-wide genotyping array 2019-03-27 30718454 Arnau-Soler A 2019-02-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30718454 Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Depressive symptoms x stressful life events interaction (1df test) 103,976 European ancestry individuals NA Affymetrix, Illumina [1009208] (imputed) 0 depressive symptom measurement, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007781 GCST007408 Genome-wide genotyping array 2019-03-27 30718454 Arnau-Soler A 2019-02-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30718454 Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Depressive symptoms x stressful life events interaction (2df test) 103,976 European ancestry individuals NA Affymetrix, Illumina [1009208] (imputed) 0 depressive symptom measurement, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007781 GCST007409 Genome-wide genotyping array 2019-03-27 30718454 Arnau-Soler A 2019-02-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30718454 Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Depressive symptoms x dependent stressful life events interaction (1df test) 4,919 European ancestry individuals NA Illumina [560351] 12 depressive symptom measurement, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007781 GCST007410 Genome-wide genotyping array 2019-03-27 30718454 Arnau-Soler A 2019-02-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30718454 Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Depressive symptoms x dependent stressful life events interaction (2df test) 4,919 European ancestry individuals NA Illumina [560351] 11 depressive symptom measurement, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007781 GCST007411 Genome-wide genotyping array 2019-03-27 30718454 Arnau-Soler A 2019-02-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30718454 Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Depressive symptoms x independent stressful life events interaction (1df test) 4,919 European ancestry individuals NA Illumina [560351] 9 depressive symptom measurement, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007781 GCST007412 Genome-wide genotyping array 2019-03-27 30718454 Arnau-Soler A 2019-02-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30718454 Genome-wide by environment interaction studies of depressive symptoms and psychosocial stress in UK Biobank and Generation Scotland. Depressive symptoms x independent stressful life events interaction (2df test) 4,919 European ancestry individuals NA Illumina [560351] 8 depressive symptom measurement, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007006, http://www.ebi.ac.uk/efo/EFO_0007781 GCST007413 Genome-wide genotyping array 2019-08-20 31308545 Watson HJ 2019-07-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31308545 Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa. Anorexia nervosa 16,992 European ancestry cases, 55,525 European ancestry controls NA Affymetrix, Illumina [at least 8111819] (imputed) 8 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST008465 Genome-wide genotyping array 2019-02-28 30557369 Yodsurang V 2018-12-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/30557369 Genome-wide association study (GWAS) of ovarian cancer in Japanese predicted regulatory variants in 22q13.1. Ovarian cancer 681 Japanese ancestry cases, 17,492 Japanese ancestry controls NA Illumina [7521072] (imputed) 28 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST007239 Genome-wide genotyping array 2019-04-09 30525989 Siewert KM 2018-12-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/30525989 Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease. Coronary artery disease and HDL cholesterol levels (multivariate analysis) 122,733 coronary artery disease cases, 424,528 coronary artery disease controls, 188,577 individuals NA NR [NR] 1 high density lipoprotein cholesterol measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0001645 GCST007547 Genome-wide genotyping array 2019-04-09 30525989 Siewert KM 2018-12-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/30525989 Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease. Coronary artery disease and LDL cholesterol levels (multivariate analysis) 122,733 coronary artery disease cases, 424,528 coronary artery disease controls, 188,577 individuals NA NR [NR] 2 low density lipoprotein cholesterol measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0001645 GCST007546 Genome-wide genotyping array 2019-04-09 30525989 Siewert KM 2018-12-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/30525989 Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease. Coronary artery disease and triglyceride levels (multivariate analysis) 122,733 coronary artery disease cases, 424,528 coronary artery disease controls, 188,577 individuals NA NR [NR] 3 triglyceride measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0001645 GCST007545 Genome-wide genotyping array 2019-04-09 30525989 Siewert KM 2018-12-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/30525989 Bivariate Genome-Wide Association Scan Identifies 6 Novel Loci Associated With Lipid Levels and Coronary Artery Disease. Coronary artery disease and total cholesterol levels (multivariate analysis) 122,733 coronary artery disease cases, 424,528 coronary artery disease controls, 188,577 individuals NA NR [NR] 1 total cholesterol measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0001645 GCST007544 Genome-wide genotyping array 2019-01-21 30563984 Hawi Z 2018-12-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30563984 A case-control genome-wide association study of ADHD discovers a novel association with the tenascin R (TNR) gene. Attention deficit hyperactivity disorder 480 European ancestry cases, 1,208 European ancestry controls NA Illumina [5407269] (imputed) 14 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST006916 Genome-wide genotyping array 2019-05-02 30556296 Alblooshi H 2018-12-16 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/30556296 A case-control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE). Substance use disorder 249 Arabian ancestry cases, 253 Arabian ancestry controls 415 European ancestry cases, 105 European ancestry controls Illumina [1879623] 1 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST007700 Genome-wide genotyping array 2019-01-15 30320955 Baird DA 2018-10-15 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30320955 Identification of novel loci associated with hip shape: a meta-analysis of genome-wide association studies. Hip shape (DXA scan) 10,217 European ancestry individuals, 5,717 individuals NA Illumina [7191926] (imputed) 12 hip geometry http://www.ebi.ac.uk/efo/EFO_0004685 GCST006903 Genome-wide genotyping array 2019-02-15 25224099 Gueant JL 2014-09-12 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/25224099 HLA-DRA variants predict penicillin allergy in genome-wide fine-mapping genotyping. beta-lactam allergy measurement 387 European ancestry cases, 1,224 European ancestry controls 299 European ancestry cases, 362 European ancestry controls Illumina [107398] 0 beta-lactam allergy measurement http://www.ebi.ac.uk/efo/EFO_0009694 GCST007161 Targeted genotyping array [ImmunoChip] 2020-09-18 32888494 Vuckovic D 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888494 The Polygenic and Monogenic Basis of Blood Traits and Diseases. Red cell distribution width 408,112 British individuals NA Affymetrix [93095623] (imputed) 593 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90002404 Genome-wide genotyping array 2020-09-18 32888494 Vuckovic D 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888494 The Polygenic and Monogenic Basis of Blood Traits and Diseases. Reticulocyte count 408,112 British individuals NA Affymetrix [93095623] (imputed) 604 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90002405 Genome-wide genotyping array 2020-09-18 32888494 Vuckovic D 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888494 The Polygenic and Monogenic Basis of Blood Traits and Diseases. Reticulocyte fraction of red cells 408,112 British individuals NA Affymetrix [93095623] (imputed) 584 reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0010700 GCST90002406 Genome-wide genotyping array 2020-09-18 32888494 Vuckovic D 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888494 The Polygenic and Monogenic Basis of Blood Traits and Diseases. White blood cell count 408,112 British individuals NA Affymetrix [93095623] (imputed) 668 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90002407 Genome-wide genotyping array 2019-09-02 31190057 Dashti HS 2019-06-13 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31190057 Genome-wide association study of breakfast skipping links clock regulation with food timing. Breakfast cereal skipping frequency 193,860 European ancestry individuals NA Affymetrix [up to 73355667] (imputed) 6 breakfast skipping measurement http://www.ebi.ac.uk/efo/EFO_0010129 GCST008555 Genome-wide genotyping array 2019-09-02 31190057 Dashti HS 2019-06-13 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31190057 Genome-wide association study of breakfast skipping links clock regulation with food timing. Breakfast skipping 1,359 European ancestry cases, 10,604 European ancestry controls NA Affymetrix, Illumina [up to 38050714] (imputed) 6 breakfast skipping measurement http://www.ebi.ac.uk/efo/EFO_0010129 GCST008556 Genome-wide genotyping array 2019-09-05 31320941 Igarashi M 2019-07-05 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/31320941 Identification of the 12q24 locus associated with fish intake frequency by genome-wide meta-analysis in Japanese populations. Fish intake frequency 12,603 Japanese ancestry individuals NA Illumina [296675] 4 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST008597 Genome-wide genotyping array 2020-02-06 31668730 Cintho Ozahata M 2019-10-24 J Sex Med www.ncbi.nlm.nih.gov/pubmed/31668730 Clinical and Genetic Predictors of Priapism in Sickle Cell Disease: Results from the Recipient Epidemiology and Donor Evaluation Study III Brazil Cohort Study. Priapism in sickle cell disease 169 European, African, Hispanic or unknown ancestry cases, 433 European, African, Hispanic or unknown ancestry controls NA Affymetrix [831797] (imputed) 2 Priapism http://purl.obolibrary.org/obo/HP_0200023 GCST009550 Genome-wide genotyping array 2019-05-22 30718926 Suzuki K 2019-02-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30718926 Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. Type 2 diabetes 36,614 Japanese ancestry cases, 155,150 Japanese ancestry controls NA Illumina [12557761] (imputed) 126 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007847 Genome-wide genotyping array 2019-02-08 30664745 Tachmazidou I 2019-01-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30664745 Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Knee osteoarthritis 24,955 European ancestry cases, 378,169 European ancestry controls NA Affymetrix, Illumina [up to 17000000] (imputed) 13 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST007090 Genome-wide genotyping array 2019-02-08 30664745 Tachmazidou I 2019-01-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30664745 Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Osteoarthritis (hip) 15,704 European ancestry cases, 378,169 European ancestry controls NA Affymetrix, Illumina [up to 17000000] (imputed) 29 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST007091 Genome-wide genotyping array 2019-02-08 30664745 Tachmazidou I 2019-01-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30664745 Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Osteoarthritis of the hip or knee 39,427 European ancestry cases, 378,169 European ancestry controls NA Affymetrix, Illumina [up to 17000000] (imputed) 30 osteoarthritis, hip, osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616 GCST007092 Genome-wide genotyping array 2019-02-08 30664745 Tachmazidou I 2019-01-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30664745 Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. Osteoarthritis 77,052 European ancestry cases, 378,169 European ancestry controls NA Affymetrix, Illumina [up to 17000000] (imputed) 35 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST007093 Genome-wide genotyping array 2019-08-07 31196165 Lee E 2019-06-13 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/31196165 Genome-wide enriched pathway analysis of acute post-radiotherapy pain in breast cancer patients: a prospective cohort study. Acute post-radiotherapy pain in breast cancer 136 Hispanic cases, 75 European ancestry cases, 102 African ancestry cases, 45 cases, 265 Hispanic controls, 282 European ancestry controls, 194 African ancestry controls, 45 controls NA Illumina [1344832] (imputed) 3 response to radiation, pain http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0003843 GCST008388 Genome-wide genotyping array 2022-07-13 35401282 Vollert J 2022-03-23 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35401282 Genotypes of Pain and Analgesia in a Randomized Trial of Irritable Bowel Syndrome. Response to treatment in irritable bowel syndrome (pain frequency) 22 European ancestry double-blind peppermint oil-treated individuals, 53 European ancestry double-blind placebo-treated individuals, 52 European ancestry open-label placebo-treated individuals, 52 European ancestry no pill control-treated individuals, 4 double-blind peppermint oil-treated individuals, 9 double-blind placebo-treated individuals, 10 open-label placebo-treated individuals, 10 no pill control-treated individuals NA Illumina [729526] 14 irritable bowel syndrome symptom measurement http://www.ebi.ac.uk/efo/EFO_0021536 GCST90104793 Genome-wide genotyping array 2022-07-13 35401282 Vollert J 2022-03-23 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35401282 Genotypes of Pain and Analgesia in a Randomized Trial of Irritable Bowel Syndrome. Response to treatment in irritable bowel syndrome (pain severity) 22 European ancestry double-blind peppermint oil-treated individuals, 53 European ancestry double-blind placebo-treated individuals, 52 European ancestry open-label placebo-treated individuals, 52 European ancestry no pill control-treated individuals, 4 double-blind peppermint oil-treated individuals, 9 double-blind placebo-treated individuals, 10 open-label placebo-treated individuals, 10 no pill control-treated individuals NA Illumina [729526] 14 irritable bowel syndrome symptom measurement http://www.ebi.ac.uk/efo/EFO_0021536 GCST90104792 Genome-wide genotyping array 2019-07-18 31194788 Read RW 2019-06-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/31194788 GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort. Mean platelet volume Up to 53 African American individuals, 100 Asian ancestry individuals, 4,175 European ancestry individuals, 138 Hispanic or Latin American individuals, 30 Native American individuals, 11 Pacific Islander ancestry individuals, 168 unknown ancestry individuals NA Illumina [498916] 5 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST008167 Genome-wide genotyping array 2019-07-18 31194788 Read RW 2019-06-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/31194788 GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort. Mean corpuscular volume Up to 53 African American individuals, 100 Asian ancestry individuals, 4,175 European ancestry individuals, 138 Hispanic or Latin American individuals, 30 Native American individuals, 11 Pacific Islander ancestry individuals, 168 unknown ancestry individuals NA Illumina [498916] 3 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST008166 Genome-wide genotyping array 2019-07-18 31194788 Read RW 2019-06-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/31194788 GWAS and PheWAS of red blood cell components in a Northern Nevadan cohort. Platelet count 53 African American individuals, 100 Asian ancestry individuals, 4,175 European ancestry individuals, 138 Hispanic or Latin American individuals, 30 Native American individuals, 11 Pacific Islander ancestry individuals, 168 unknown ancestry individuals NA Illumina [498916] 1 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST008168 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Corneal hysteresis 6,125 Icelandic ancestry individuals NA Illumina [NR] 9 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST008315 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Corneal resistance factor 6,125 Icelandic ancestry individuals NA Illumina [NR] 9 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST008318 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Intraocular pressure (corneal compensated) 6,125 Icelandic ancestry individuals NA Illumina [NR] 1 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST008319 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Intraocular pressure (Goldman correlated) 6,125 Icelandic ancestry individuals NA Illumina [NR] 3 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST008320 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Central corneal thickness 6,125 Icelandic ancestry individuals 1,459 Icelandic ancestry individuals Illumina [NR] 11 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST008317 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Corneal endothelial cell density 6,125 Icelandic ancestry individuals NA Illumina [NR] 58 corneal endothelial cell measurement http://www.ebi.ac.uk/efo/EFO_0010079 GCST008339 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Corneal endothelial cell size variation coefficient 6,125 Icelandic ancestry individuals NA Illumina [NR] 39 corneal endothelial cell measurement http://www.ebi.ac.uk/efo/EFO_0010079 GCST008316 Genome-wide genotyping array 2019-08-02 30894546 Ivarsdottir EV 2019-03-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30894546 Sequence variation at ANAPC1 accounts for 24% of the variability in corneal endothelial cell density. Corneal endothelial cell shape (percentage of hexagonally shaped cells) 6,125 Icelandic ancestry individuals NA Illumina [NR] 21 corneal endothelial cell measurement http://www.ebi.ac.uk/efo/EFO_0010079 GCST008321 Genome-wide genotyping array 2020-10-08 32769997 Zhou W 2020-08-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32769997 GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer. Thyroid stimulating hormone levels 119,715 European ancestry individuals NA Illumina [22400000] (imputed) 99 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST010653 Genome-wide genotyping array 2019-07-26 30845926 van der Plaat DA 2019-03-07 BMC Pulm Med www.ncbi.nlm.nih.gov/pubmed/30845926 Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population. Airway obstruction (FEV1/FVC<70%) in never smokers 77 European ancestry cases, 355 European ancestry controls NA Illumina [242926] 3 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST008240 Genome-wide genotyping array 2019-07-26 30845926 van der Plaat DA 2019-03-07 BMC Pulm Med www.ncbi.nlm.nih.gov/pubmed/30845926 Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population. Airway obstruction (FEV1/FVC 445ms female individuals, 100 European ancestry < 386ms female individuals 200 European ancestry > 85th pct female individuals, 200 European ancestry < 15th pct female individuals, 4,451 European ancestry individuals Affymetrix [88500] 1 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST000004 Genome-wide genotyping array 2015-04-24 21239051 Reilly MP 2011-01-14 Lancet www.ncbi.nlm.nih.gov/pubmed/21239051 Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Coronary artery disease 1,808 European ancestry cases, 915 European ancestry controls 10,585 European ancestry cases, 6,468 European ancestry controls Affymetrix, Illumina [> 2400000] (imputed) 3 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000945 Genome-wide genotyping array 2015-04-24 21239051 Reilly MP 2011-01-14 Lancet www.ncbi.nlm.nih.gov/pubmed/21239051 Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Myocardial infarction in coronary artery disease 4,572 European ancestry cases, 2,739 European ancestry controls 1,211 European ancestry cases, 905 European ancestry controls Affymetrix, Illumina [up to 2400000] (imputed) 1 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST000946 Genome-wide genotyping array 2015-04-20 21292315 Nalls MA 2011-02-01 Lancet www.ncbi.nlm.nih.gov/pubmed/21292315 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Parkinson's disease 5,333 European ancestry cases, 12,019 European ancestry controls 7,053 cases, 9,007 controls Illumina [7689524] (imputed) 11 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000959 Genome-wide genotyping array 2015-05-15 21347284 Smith JG 2011-02-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21347284 Genome-wide association studies of the PR interval in African Americans. PR interval 6,247 African American individuals 2,022 African American individuals Affymetrix [2801419] (imputed) 5 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST000971 Genome-wide genotyping array 2008-06-26 18535201 Cooper GM 2008-06-05 Blood www.ncbi.nlm.nih.gov/pubmed/18535201 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. Warfarin maintenance dose 181 European ancestry individuals 374 European ancestry individuals Illumina [538629] 3 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST000204 Genome-wide genotyping array 2010-04-12 20306291 Davis OS 2010-03-21 Behav Genet www.ncbi.nlm.nih.gov/pubmed/20306291 A three-stage genome-wide association study of general cognitive ability: hunting the small effects. Cognitive ability 860 European ancestry children 2,619 European ancestry children Affymetrix [358948] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST000634 Genome-wide genotyping array 2010-09-21 20705733 O'Seaghdha CM 2010-08-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20705733 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. Calcium levels 20,611 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 10 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST000769 Genome-wide genotyping array 2009-04-01 19303062 Tanaka T 2009-03-18 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19303062 Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations. Folate pathway vitamin levels 2,934 European ancestry individuals 686 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 5 vitamin B measurement, vitamin B12 measurement, vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004843, http://www.ebi.ac.uk/efo/EFO_0004620, http://www.ebi.ac.uk/efo/EFO_0004621 GCST000358 Genome-wide genotyping array 2010-09-27 20808326 Krumbiegel M 2010-09-01 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20808326 Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. Pseudoexfoliation syndrome 160 European ancestry cases, 80 European ancestry controls 859 European ancestry cases, 554 European ancestry controls Affymetrix [~ 500000] 0 exfoliation syndrome http://www.ebi.ac.uk/efo/EFO_0004235 GCST000784 Genome-wide genotyping array 2010-10-05 20835239 Solouki AM 2010-09-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20835239 A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. Refractive error 5,328 European ancestry individuals 10,280 European ancestry individuals Illumina [~ 2500000] (imputed) 1 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST000795 Genome-wide genotyping array 2013-09-21 20117844 Brynedal B 2010-02-01 J Neuroimmunol www.ncbi.nlm.nih.gov/pubmed/20117844 MGAT5 alters the severity of multiple sclerosis. Multiple sclerosis (severity) 1,040 European ancestry cases 873 European ancestry cases Affymetrix [105035] 1 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000577 Genome-wide genotyping array 2009-02-05 19081515 Mead S 2008-12-11 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/19081515 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. Creutzfeldt-Jakob disease 117 European ancestry cases, 3,083 European ancestry controls 2 European ancestry vCJD cases, 506 Oceania ancestry sCJD cases, 28 Oceania ancestry iCJD cases, 151 Oceania ancestry Kuru cases, 125 Oceania ancestry Kuru resistant cases, 3,608 European ancestry controls, 562 Oceania ancestry controls Affymetrix [288908] 2 Creutzfeldt Jacob Disease http://www.ebi.ac.uk/efo/EFO_0004226 GCST000294 Genome-wide genotyping array 2009-02-28 19198613 Gudmundsson J 2009-02-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19198613 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. Thyroid cancer 192 European ancestry cases, 37,196 European ancestry controls 432 European ancestry cases, 1,727 European ancestry controls Illumina [304083] 2 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST000335 Genome-wide genotyping array 2011-01-12 21123754 Kim S 2010-12-01 Neurology www.ncbi.nlm.nih.gov/pubmed/21123754 Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort. Alzheimer's disease biomarkers 96 European ancestry Alzheimer disease cases, 176 European ancestry individuals with mild cognitive impairment, 102 European ancestry controls NA Illumina [322557] 7 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000900 Genome-wide genotyping array 2013-11-13 23696099 Ding K 2013-05-20 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/23696099 Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study. Red blood cell traits 1904 African American individuals 411 African American individuals Illumina [907954] 7 erythrocyte indices http://www.ebi.ac.uk/efo/EFO_0004306 GCST002027 Genome-wide genotyping array 2009-01-12 19060906 Kathiresan S 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060906 Common variants at 30 loci contribute to polygenic dyslipidemia. HDL cholesterol 19,840 European ancestry individuals Up to 20,623 European ancestry individuals Affymetrix, Illumina [~ 2600000] (imputed) 14 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000290 Genome-wide genotyping array 2009-01-14 19060906 Kathiresan S 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060906 Common variants at 30 loci contribute to polygenic dyslipidemia. LDL cholesterol 19,840 European ancestry individuals Up to 20,623 European ancestry individuals Affymetrix, Illumina [~ 2600000] (imputed) 11 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000287 Genome-wide genotyping array 2009-01-12 19060906 Kathiresan S 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060906 Common variants at 30 loci contribute to polygenic dyslipidemia. Triglycerides 19,840 European ancestry individuals Up to 20,623 European ancestry individuals Affymetrix, Illumina [~ 2600000] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000286 Genome-wide genotyping array 2009-03-01 19198612 Erdmann J 2009-02-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19198612 New susceptibility locus for coronary artery disease on chromosome 3q22.3. Coronary heart disease 1,222 European ancestry cases, 1,298 European ancestry controls 18,185 European ancestry cases, 20,068 European ancestry controls Affymetrix [567119] 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000338 Genome-wide genotyping array 2010-09-10 20686608 Low SK 2010-07-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/20686608 Genome-wide association study of pancreatic cancer in Japanese population. Pancreatic cancer 991 Japanese ancestry cases, 5,209 Japanese ancestry controls NA Illumina [420236] 17 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST000745 Genome-wide genotyping array 2009-02-25 19165155 Ling H 2009-01-22 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/19165155 Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. Adiponectin levels 997 European ancestry cases, 989 European ancestry controls NA Affymetrix [398625] 2 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST000319 Genome-wide genotyping array 2009-02-28 19187332 Kim SH 2009-02-01 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/19187332 Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. Asthma (toluene diisocyanate-induced) 84 Korean ancestry cases, 263 Korean ancestry controls NA Affymetrix [312978] 3 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000330 Genome-wide genotyping array 2009-02-04 19107115 Muglia P 2008-12-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19107115 Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. Major depressive disorder 1,359 European ancestry cases, 1,782 European ancestry controls NA Affymetrix, Illumina [494678] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST000304 Genome-wide genotyping array 2010-02-08 20081857 Saxena R 2010-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20081857 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Two-hour glucose challenge 15,234 individuals up to 30,620 European ancestry individuals Affymetrix, Illumina [NR] 5 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST000569 Genome-wide genotyping array 2008-06-16 18264096 Thomas G 2008-02-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18264096 Multiple loci identified in a genome-wide association study of prostate cancer. Prostate cancer 1,172 European ancestry cases, 1,157 European ancestry controls 3,941 European ancestry cases, 3,964 European ancestry controls Illumina [527869] 7 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000154 Genome-wide genotyping array 2009-03-01 19230858 Schrauwen I 2009-02-18 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19230858 A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. Otosclerosis 302 cases, 302 controls 847 cases, 872 controls Illumina [~ 555000] 1 otosclerosis http://www.ebi.ac.uk/efo/EFO_0004213 GCST000345 Genome-wide genotyping array 2012-08-14 22688191 Bergen SE 2012-06-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22688191 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. Schizophrenia 2,111 European ancestry cases, 2,535 European ancestry controls 11,271 European ancestry cases, 14,601 European ancestry controls Affymetrix [745006] 15 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001565 Genome-wide genotyping array 2012-08-14 22688191 Bergen SE 2012-06-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22688191 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. Bipolar disorder and schizophrenia 2,111 European ancestry schizophrenia cases, 836 European ancestry bipolar disorder cases, 2,535 European ancestry controls NA Affymetrix [745006] 13 bipolar disorder, schizophrenia http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST001567 Genome-wide genotyping array 2012-08-14 22688191 Bergen SE 2012-06-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22688191 Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder. Bipolar disorder 836 European ancestry cases, 2,093 European ancestry controls NA Affymetrix [745006] 4 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001569 Genome-wide genotyping array 2012-11-04 22895189 Timmann C 2012-08-15 Nature www.ncbi.nlm.nih.gov/pubmed/22895189 Genome-wide association study indicates two novel resistance loci for severe malaria. Malaria 1,325 African ancestry, 828 African ancestry controls 2,229 African ancestry cases, 3,526 African ancestry controls Affymetrix [4205739] (imputed) 4 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST001637 Genome-wide genotyping array 2011-10-04 21931568 Geller F 2011-09-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21931568 Genome-wide association study identifies four loci associated with eruption of permanent teeth. Permanent tooth development 5,088 European ancestry females 2,994 European ancestry individuals, 161 individuals Illumina [521741] 4 tooth eruption http://purl.obolibrary.org/obo/GO_0044691 GCST001221 Genome-wide genotyping array 2012-09-18 22797727 Okada Y 2012-07-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22797727 Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Renal function-related traits (BUN) 39,717 East Asian ancestry individuals 17,461 East Asian ancestry individuals Affymetrix, Illumina [2281523] (imputed) 15 renal system measurement, blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004742, http://www.ebi.ac.uk/efo/EFO_0004741 GCST001610 Genome-wide genotyping array 2012-09-18 22797727 Okada Y 2012-07-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22797727 Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Renal function-related traits (sCR) 42,257 East Asian, South Asian, and South East Asian ancestry individuals 19,662 East Asian ancestry individuals Affymetrix, Illumina [2353587] (imputed) 9 renal system measurement http://www.ebi.ac.uk/efo/EFO_0004742 GCST001606 Genome-wide genotyping array 2012-09-18 22797727 Okada Y 2012-07-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22797727 Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Renal function-related traits (eGRFcrea) 42,451 East Asian, South Asian, and South East Asian ancestry individuals 19,636 East Asian ancestry individuals Affymetrix, Illumina [2353587] (imputed) 10 renal system measurement http://www.ebi.ac.uk/efo/EFO_0004742 GCST001607 Genome-wide genotyping array 2012-09-18 22797727 Okada Y 2012-07-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22797727 Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Renal function-related traits (urea) 21,417 East Asian ancestry individuals 11,657 East Asian ancestry individuals Affymetrix, Illumina [2278301] (imputed) 4 renal system measurement, uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004742, http://www.ebi.ac.uk/efo/EFO_0004761 GCST001608 Genome-wide genotyping array 2012-05-24 22479191 Pattaro C 2012-03-29 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22479191 Genome-wide association and functional follow-up reveals new loci for kidney function. Chronic kidney disease 74,354 European ancestry individuals 56,246 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST001466 Genome-wide genotyping array 2013-06-20 23472165 Albertsen HM 2013-03-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/23472165 Genome-wide association study link novel loci to endometriosis. Endometriosis 1,514 European ancestry cases, 12,660 European ancestry controls 505 European ancestry cases, 1,811 European ancestry controls Illumina [580699] 15 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST001894 Genome-wide genotyping array 2009-12-28 19950302 Zhou X 2009-11-30 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/19950302 HLA-DPB1 and DPB2 are genetic loci for systemic sclerosis: a genome-wide association study in Koreans with replication in North Americans. Systemic sclerosis 133 Korean ancestry cases, 557 Korean ancestry controls 1,107 European ancestry cases, 2,747 European ancestry controls Affymetrix [440734] 0 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST000535 Genome-wide genotyping array 2013-06-16 23474815 Stambolian D 2013-03-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23474815 Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Refractive error 6,597 European ancestry and Erasmus Rucphen individuals, 683 Sardinian inidividuals 19,763 European ancestry individuals Affymetrix, Illumina [2093862] (imputed) 1 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST001898 Genome-wide genotyping array 2012-08-14 22726844 Kim JW 2012-06-20 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22726844 A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval. QT interval 6,805 Korean ancestry individuals 7,373 East Asian ancestry individuals Affymetrix [352228] 3 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST001580 Genome-wide genotyping array 2013-06-06 23468962 Song C 2013-02-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/23468962 A genome-wide scan for breast cancer risk haplotypes among African American women. Breast cancer 3,016 African American cases, 2,745 African American controls NA Illumina [1006480] 13 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001879 Genome-wide genotyping array 2013-05-16 23372042 Lane J 2013-02-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23372042 A genome-wide association study of resistance to HIV infection in highly exposed uninfected individuals with hemophilia A. HIV-1 susceptibility 430 European ancestry HIV exposed uninfected Haemophilia cases, 765 European ancestry HIV positive controls NA Illumina [1081435] (imputed) 0 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST001857 Genome-wide genotyping array 2012-08-14 22685421 Fan Q 2012-06-07 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22685421 Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. Myopia (pathological) 2,789 Chinese ancestry individuals, 2,155 Malay ancestry individuals NA Illumina [456634] 4 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST001561 Genome-wide genotyping array 2009-07-24 19570815 Estrada K 2009-07-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19570815 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. Height 10,074 European ancestry individuals 6,912 European ancestry individuals Affymetrix, Illumina, Perlegen [2228850] (imputed) 5 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000431 Genome-wide genotyping array 2013-02-08 23223146 Le Clerc S 2012-12-06 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/23223146 A genome-wide association study in Caucasian women points out a putative role of the STXBP5L gene in facial photoaging. Aging (facial) 502 European ancestry females NA Illumina [795063] 4 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST001767 Genome-wide genotyping array 2008-06-16 17158188 Bierut LJ 2006-12-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/17158188 Novel genes identified in a high-density genome wide association study for nicotine dependence. Nicotine dependence 482 European ancestry cases, 466 European ancestry controls 568 European ancestry cases, 413 European ancestry controls Perlegen [2400000] 2 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST000010 Genome-wide genotyping array 2011-01-08 21107343 Aoki A 2010-11-25 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21107343 SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population. Myocardial infarction 194 Japanese ancestry cases, 1,539 Japanese ancestry controls 5,177 Japanese ancestry cases, 6,220 Japanese ancestry controls Perlegen [210785] 1 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST000887 Genome-wide genotyping array 2008-09-12 18758464 Kugathasan S 2008-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18758464 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. Inflammatory bowel disease 1,011 European ancestry cases, 4,250 European ancestry controls 1,922 European ancestry cases, 14,124 European ancestry controls Illumina [NR] 6 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST000225 Genome-wide genotyping array 2008-09-12 18057069 Cronin S 2007-12-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/18057069 A genome-wide association study of sporadic ALS in a homogenous Irish population. Amyotrophic lateral sclerosis 221 Genetically Homogenous Irish cases, 211 Genetically Homogenous Irish controls 737 European ancestry cases, 721 European ancestry controls Illumina [497917] 1 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000126 Genome-wide genotyping array 2008-06-11 17362836 Schymick JC 2007-02-20 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/17362836 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. Amyotrophic lateral sclerosis 276 European ancestry cases, 271 European ancestry controls NA Illumina [549062] 6 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000013 Genome-wide genotyping array 2012-02-28 22286219 Kettunen J 2012-01-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22286219 Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Metabolite levels 8,330 European ancestry individuals NA Illumina [~ 7700000] (imputed) 13 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST001391 Genome-wide genotyping array 2012-02-28 22286219 Kettunen J 2012-01-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22286219 Genome-wide association study identifies multiple loci influencing human serum metabolite levels. Lipid metabolism phenotypes 8,330 European ancestry individuals NA Illumina [~ 7700000] (imputed) 18 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST001392 Genome-wide genotyping array 2008-09-03 18758461 Di Bernardo MC 2008-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18758461 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. Chronic lymphocytic leukemia 505 European ancestry cases, 1,438 European ancestry controls 1,024 European ancestry cases, 1,677 European ancestry controls Illumina [345665] 6 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST000224 Genome-wide genotyping array 2010-05-24 20418889 Liu JZ 2010-04-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20418889 Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Smoking behavior 41,150 European ancestry individuals 120,516 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST000668 Genome-wide genotyping array 2010-09-28 20838585 Smith EN 2010-09-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20838585 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. Cardiovascular risk factors (age interaction) 525 European ancestry individuals 2,442 Finnish ancestry individuals Illumina [2173391] (imputed) 4 waist circumference, triglyceride measurement, low density lipoprotein cholesterol measurement, cardiovascular disease, high density lipoprotein cholesterol measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0008007 GCST000789 Genome-wide genotyping array 2017-09-12 20838585 Smith EN 2010-09-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20838585 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. Cardiovascular risk factors 525 European ancestry individuals 2,442 Finnish ancestry individuals Illumina [2173391] (imputed) 2 waist circumference, triglyceride measurement, low density lipoprotein cholesterol measurement, cardiovascular disease, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0004612 GCST004704 Genome-wide genotyping array 2011-05-28 21552555 Wang K 2011-04-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/21552555 A genome-wide association study on obesity and obesity-related traits. Obesity 520 European ancestry cases, 540 European ancestry controls 1,196 European ancestry individuals Illumina [~ 550000] 14 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001057 Genome-wide genotyping array 2009-09-09 19714205 Hancock DB 2009-08-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19714205 Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. Asthma (childhood onset) 492 Mexican ancestry trios 177 Mexican ancestry trios Illumina [520767] 1 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST000468 Genome-wide genotyping array 2008-09-12 18776911 Hazra A 2008-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18776911 Common variants of FUT2 are associated with plasma vitamin B12 levels. Vitamin B12 levels 1,658 European ancestry female individuals 1,059 European ancestry female individuals Illumina [528134] 1 vitamin B12 measurement http://www.ebi.ac.uk/efo/EFO_0004620 GCST000228 Genome-wide genotyping array 2008-07-22 17223258 Spinola M 2007-01-16 Cancer Lett www.ncbi.nlm.nih.gov/pubmed/17223258 Genome-wide single nucleotide polymorphism analysis of lung cancer risk detects the KLF6 gene. Lung cancer 338 European ancestry lung adenocarcinoma cases, 335 European ancestry controls 265 European ancestry non-small cell lung carcinoma cases, 356 European ancestry controls Affymetrix [~ 116204] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000011 Genome-wide genotyping array 2009-10-30 19820697 Soranzo N 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19820697 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Mean platelet volume 4,627 European ancestry individuals 9,316 European ancestry individuals Affymetrix, Illumina [~ 2110000] (imputed) 15 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST000497 Genome-wide genotyping array 2009-10-30 19820697 Soranzo N 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19820697 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Hematological parameters 4,627 European ancestry individuals 9,316 European ancestry individuals Affymetrix, Illumina [~ 2110000] (imputed) 12 leukocyte count, erythrocyte count, mean corpuscular volume, mean corpuscular hemoglobin, platelet count http://www.ebi.ac.uk/efo/EFO_0004308, http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004527, http://www.ebi.ac.uk/efo/EFO_0004309 GCST000498 Genome-wide genotyping array 2012-08-07 22683750 Sinner MF 2012-06-06 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/22683750 A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern. Early cardiac repolarization 7,482 European ancestry individuals 7,151 European ancestry individuals Affymetrix, Illumina [2523555] (imputed) 3 early cardiac repolarization measurement http://www.ebi.ac.uk/efo/EFO_0004885 GCST001559 Genome-wide genotyping array 2009-09-28 19721433 McClay JL 2009-09-01 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19721433 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. Response to antipsychotic treatment 494 European ancestry cases, 244 African American and other ancestry cases NA Affymetrix, Perlegen [492900] 9 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST000473 Genome-wide genotyping array 2012-01-11 22116950 Schuh-Huerta SM 2011-11-24 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/22116950 Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women. Ovarian reserve 232 European ancestry female individuals, 200 African American female individuals NA Affymetrix [677261] 7 ovarian reserve http://www.ebi.ac.uk/efo/EFO_0004770 GCST001330 Genome-wide genotyping array 2009-08-07 19584346 Vasan RS 2009-07-08 JAMA www.ncbi.nlm.nih.gov/pubmed/19584346 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. Aortic root size 12,612 European ancestry individuals 4,094 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 6 aortic root size http://www.ebi.ac.uk/efo/EFO_0005037 GCST000442 Genome-wide genotyping array 2009-08-07 19584346 Vasan RS 2009-07-08 JAMA www.ncbi.nlm.nih.gov/pubmed/19584346 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. Cardiac structure and function 12,612 European ancestry individuals 4,094 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 4 cardiovascular measurement http://www.ebi.ac.uk/efo/EFO_0004298 GCST000441 Genome-wide genotyping array 2009-12-10 19915574 Imielinski M 2009-11-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19915574 Common variants at five new loci associated with early-onset inflammatory bowel disease. Inflammatory bowel disease (early onset) 2,413 European ancestry cases, 6,158 European ancestry controls 1,013 European ancestry cases, 5,805 European ancestry controls Illumina [~ 500000] 4 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST000531 Genome-wide genotyping array 2008-09-09 17668382 Salonen JT 2007-06-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/17668382 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. Type 2 diabetes 201 Finland founder cases, 200 Finland founder controls, 200 Ashkenazi Jewish cases, 197 Ashkenazi Jewish controls, 99 European ancestry cases, 100 European ancestry controls 2,573 European ancestry cases, 2,776 European ancestry controls Illumina [315917] 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000049 Genome-wide genotyping array 2009-09-04 19648918 Amundadottir L 2009-08-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19648918 Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. Pancreatic cancer 1,771 European ancestry cases, 1,805 European ancestry controls 2,120 European ancestry cases, 2,127 European ancestry controls Illumina [558542] 1 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST000456 Genome-wide genotyping array 2009-08-04 19597492 Benjamin EJ 2009-07-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19597492 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Atrial fibrillation 3,413 cases, 37,105 referents 2,145 cases, 4,073 controls Affymetrix, Illumina [~ 2500000] (imputed) 3 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST000445 Genome-wide genotyping array 2009-06-30 19525955 Bahlo M 2009-06-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19525955 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Multiple sclerosis 1,618 European ancestry cases, 3,413 European ancestry controls 2,256 European ancestry cases, 2,310 European ancestry controls Illumina [302098] 8 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000425 Genome-wide genotyping array 2009-02-26 19176441 Yang JJ 2009-01-28 JAMA www.ncbi.nlm.nih.gov/pubmed/19176441 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. Response to treatment for acute lymphoblastic leukemia 356 European ancestry cases, 53 Black cases, 78 cases NA Affymetrix [476796] 12 acute lymphoblastic leukemia, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0000220, http://purl.obolibrary.org/obo/GO_0097327 GCST000323 Genome-wide genotyping array 2010-02-28 20101243 Petersen GM 2010-01-24 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20101243 A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33. Pancreatic cancer 3,851 European, Chinese and other ancestry cases, 3,934 European, Chinese and other ancestry controls NA Illumina [551766] 3 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST000574 Genome-wide genotyping array 2011-01-15 21149283 Oexle K 2010-12-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21149283 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. Iron status biomarkers Up to 6,616 individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 5 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST000913 Genome-wide genotyping array 2009-07-24 19581569 Treutlein J 2009-07-01 Arch Gen Psychiatry www.ncbi.nlm.nih.gov/pubmed/19581569 Genome-wide association study of alcohol dependence. Alcohol dependence 476 European ancestry cases, 1,358 European ancestry controls 1,024 European ancestry cases, 996 European ancestry controls Illumina [524396] 6 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST000432 Genome-wide genotyping array 2012-03-17 22367966 Lin X 2012-02-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22367966 Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men. Vitamin B12 levels 1,999 Han Chinese ancestry individuals 1,496 Chinese ancestry individuals Illumina [1940245] (imputed) 6 vitamin B12 measurement http://www.ebi.ac.uk/efo/EFO_0004620 GCST001424 Genome-wide genotyping array 2010-06-14 20512145 Bei JX 2010-05-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20512145 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. Nasopharyngeal carcinoma 1,583 Chinese ancestry cases, 1,894 Chinese ancestry controls 3,507 Chinese ancestry cases, 3,063 Chinese ancestry controls, 284 Chinese ancestry trios Illumina [464328] 7 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST000687 Genome-wide genotyping array 2009-06-14 19483682 Kanetsky PA 2009-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19483682 Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. Testicular cancer 277 European ancestry cases, 919 European ancestry controls 371 European ancestry cases with their 408 parents, 860 European ancestry controls Affymetrix [611254] 1 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST000416 Genome-wide genotyping array 2010-02-02 20066004 Chung CM 2010-01-12 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/20066004 A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. Angiotensin-converting enzyme activity 400 Han Chinese ancestry hypertensive cases 623 Han Chinese ancestry hypertensive cases Illumina [~ 550000] 2 angiotensin converting enzyme activity measurement http://www.ebi.ac.uk/efo/EFO_0004463 GCST000565 Genome-wide genotyping array 2009-12-03 19890347 Birlea SA 2009-11-05 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/19890347 Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8. Vitiligo 32 Romanian founder cases, 44 European ancestry controls NA Illumina [297342] 4 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST000520 Genome-wide genotyping array 2009-01-21 19148276 Tanaka T 2009-01-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19148276 Genome-wide association study of plasma polyunsaturated fatty acids in the InCHIANTI Study. Polyunsaturated fatty acid levels 1,075 European ancestry individuals 1,076 European ancestry individuals Illumina [495343] 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST000316 Genome-wide genotyping array 2010-10-12 20852632 Goode EL 2010-09-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20852632 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. Ovarian cancer 1,768 European ancestry cases, 2,354 European ancestry controls 8,709 European ancestry cases, 51,764 European ancestry controls Illumina [2056878] (imputed) 7 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST000802 Genome-wide genotyping array 2010-01-13 20010835 Hancock DB 2009-12-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20010835 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. Pulmonary function 20,890 European ancestry individuals 16,178 European ancestry individuals Affymetrix, Illumina [2534500] (imputed) 8 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST000542 Genome-wide genotyping array 2008-06-16 17603472 Gudbjartsson DF 2007-07-01 Nature www.ncbi.nlm.nih.gov/pubmed/17603472 Variants conferring risk of atrial fibrillation on chromosome 4q25. Atrial fibrillation/atrial flutter 550 European ancestry cases, 4,476 European ancestry controls 3,030 European ancestry cases, 14,780 European ancestry controls, 333 Han Chinese ancestry cases, 2,836 Han Chinese ancestry controls Illumina [316515] 2 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST000051 Genome-wide genotyping array 2011-01-14 21211798 Yamada Y 2010-12-15 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/21211798 Association of a polymorphism of BTN2A1 with myocardial infarction in East Asian populations. Myocardial infarction 134 Japanese ancestry cases, 137 Japanese ancestry controls 3,954 East Asian ancestry cases, 13,222 East Asian ancestry controls Affymetrix [~ 500000] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST000920 Genome-wide genotyping array 2011-01-27 21216876 Sharma S 2011-01-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21216876 Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. Adolescent idiopathic scoliosis 1,113 European, African, Oceania, Hispanic and other ancestry individuals from 418 families 562 European ancestry cases, 666 European ancestry controls, 137 cases, 2,126 controls Illumina [326498] 1 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST000938 Genome-wide genotyping array 2011-04-06 21357381 Figueiredo JC 2011-02-25 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/21357381 Genotype-environment interactions in microsatellite stable/microsatellite instability-low colorectal cancer: results from a genome-wide association study. Colorectal cancer 1,191 European ancestry cases, 999 European ancestry controls 872 European ancestry cases, 810 European ancestry controls Illumina [770098] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000989 Genome-wide genotyping array 2010-03-17 20174558 Tsai FJ 2010-02-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20174558 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. Type 2 diabetes 995 Han Chinese ancestry cases, 894 Han Chinese ancestry controls 1,803 Han Chinese ancestry cases, 1,473 Han Chinese ancestry controls Illumina [516737] 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000601 Genome-wide genotyping array 2010-12-09 21062454 Li J 2010-11-09 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/21062454 A genome-wide association scan on estrogen receptor-negative breast cancer. Breast cancer (estrogen-receptor negative) 617 European ancestry cases, 4,583 European ancestry controls 1,011 cases, 7,604 controls Illumina [285984] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000867 Genome-wide genotyping array 2010-10-07 20876611 Wu Y 2010-09-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20876611 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. Adiponectin levels 1,776 Filipino ancestry female individuals 1,774 Filipino ancestry offspring Affymetrix [2073674] (imputed) 3 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST000812 Genome-wide genotyping array 2010-10-05 20833655 Cha PC 2010-09-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20833655 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. Warfarin maintenance dose 807 Japanese ancestry low dose individuals, 701 Japanese ancestry high dose individuals 444 Japanese ancestry individuals Illumina [485227] 5 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST000792 Genome-wide genotyping array 2011-04-04 21359210 Ricci G 2011-02-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/21359210 Pooled genome-wide analysis to identify novel risk loci for pediatric allergic asthma. Asthma (childhood onset) 135 European ancestry asthma child cases, 134 European ancestry rhinoconjunctivitis child cases 35 asthma child cases, 44 rhinoconjunctivitis child cases Affymetrix [~ 500000] 0 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST000979 Genome-wide genotyping array 2010-10-14 20885792 Naj AC 2010-09-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20885792 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. Alzheimer's disease (late onset) 931 cases, 1,104 controls 1,338 cases, 2,003 controls Illumina [483399] 4 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000808 Genome-wide genotyping array 2011-04-06 21357676 Sulem P 2011-02-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21357676 Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. Coffee consumption 5,840 European ancestry individuals, 771 Sorbian (founder/genetic isolate) individuals 4,050 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 coffee consumption http://www.ebi.ac.uk/efo/EFO_0004330 GCST000992 Genome-wide genotyping array 2011-04-06 21364930 Bol SM 2011-02-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/21364930 Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages. HIV-1 replication 191 European ancestry individuals 31 individuals Illumina [494656] 1 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST000990 Genome-wide genotyping array 2014-03-22 24015780 Wetherill L 2013-09-09 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/24015780 Family-based association analysis of alcohol dependence criteria and severity. Alcohol dependence up to 2,322 European ancestry individuals from 118 families 2,647 European ancestry individuals Illumina [591785] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST002172 Genome-wide genotyping array 2010-04-06 20195266 Adkins DE 2010-03-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20195266 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. Response to antipsychotic treatment 421 European ancestry, 214 African American, and 103 cases NA Affymetrix [492900] 37 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST000618 Genome-wide genotyping array 2010-03-25 20185149 Athanasiu L 2010-02-23 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/20185149 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. Schizophrenia 201 European ancestry cases, 305 European ancestry controls 2,663 European ancestry cases, 13,780 European ancestry controls Affymetrix [572888] 3 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000607 Genome-wide genotyping array 2009-05-05 19359809 Hiura Y 2009-04-10 Circ J www.ncbi.nlm.nih.gov/pubmed/19359809 Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study. HDL cholesterol 900 Japanese ancestry individuals 1,810 Japanese ancestry individuals Illumina [368274] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000377 Genome-wide genotyping array 2009-07-24 19584900 Tonjes A 2009-07-08 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19584900 Association of FTO variants with BMI and fat mass in the self-contained population of Sorbs in Germany. Body mass index and fat mass 948 Sorbian (founder/genetic isolate) individuals NA Affymetrix [390619] 0 adipose tissue measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004764, http://www.ebi.ac.uk/efo/EFO_0004340 GCST000443 Genome-wide genotyping array 2009-03-24 19268274 Liu XG 2009-03-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19268274 Genome-wide association and replication studies identified TRHR as an important gene for lean body mass. Body mass (lean) 973 European ancestry individuals 1,488 European ancestry individuals, 1,972 European ancestry individuals from 593 families, 2,955 Chinese ancestry individuals Affymetrix [379319] 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST000352 Genome-wide genotyping array 2010-06-18 20520587 Nielsen DA 2010-06-01 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/20520587 Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. Heroin addiction 200 European ancestry cases, 150 European ancestry controls, 125 African American cases, 100 African American controls NA Affymetrix [up to 113174] 0 heroin dependence http://www.ebi.ac.uk/efo/EFO_0004240 GCST000690 Genome-wide genotyping array 2008-12-01 18997786 Bilguvar K 2008-11-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18997786 Susceptibility loci for intracranial aneurysm in European and Japanese populations. Intracranial aneurysm 1,580 European ancestry cases, 6,276 European ancestry controls 495 Japanese ancestry cases, 676 Japanese ancestry controls Illumina [289271] 4 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST000262 Genome-wide genotyping array 2010-05-23 20418489 Qi L 2010-04-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20418489 Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. Type 2 diabetes 2,591 European ancestry cases, 3,052 European ancestry controls 10,870 European ancestry cases, 73,735 European ancestry controls Affymetrix [683509] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000665 Genome-wide genotyping array 2008-06-16 18385738 Hung RJ 2008-04-03 Nature www.ncbi.nlm.nih.gov/pubmed/18385738 A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. Lung cancer 1,926 European ance other ancestry cases, 2,522 European and other ancestry controls 332 European ancestry cases, 462 European ancestry controls, 2,181 European and other ancestry cases, 4,290 European and other ancestry controls Illumina [310023] 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000170 Genome-wide genotyping array 2011-07-07 21665994 Kutalik Z 2011-06-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21665994 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. Alcohol consumption (transferrin glycosylation) 5,181 European ancestry individuals 2,284 European ancestry individauls Affymetrix [390631] (imputed) 6 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST001103 Genome-wide genotyping array 2008-06-16 17529967 Easton DF 2007-05-27 Nature www.ncbi.nlm.nih.gov/pubmed/17529967 Genome-wide association study identifies novel breast cancer susceptibility loci. Breast cancer 390 European ancestry cases, 364 European ancestry controls 4,364 East Asian ancestry cases, 24,174 European ancestry controls, 3,564 East Asian ancestry controls, 24,391 European ancestry controls Perlegen [205586] 6 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000035 Genome-wide genotyping array 2009-03-18 19249006 Xiong DH 2009-02-25 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19249006 Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups. Bone mineral density 1,000 European ancestry individuals 4,925 European ancestry individuals, 350 Chinese ancestry hip fracture cases, 350 Chinese ancestry hip fracture controls, 2,955 Chinese ancestry individuals, 908 West African ancestry males Affymetrix [379319] 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000347 Genome-wide genotyping array 2012-05-25 22511988 Jylhava J 2012-04-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/22511988 A genome-wide association study identifies UGT1A1 as a regulator of serum cell-free DNA in young adults: The Cardiovascular Risk in Young Finns Study. Circulating cell-free DNA 1,841 individuals NA Illumina [2543887] (imputed) 1 circulating cell free DNA measurement http://www.ebi.ac.uk/efo/EFO_0004739 GCST001478 Genome-wide genotyping array 2009-03-24 19268276 Vink JM 2009-03-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19268276 Genome-wide association study of smoking initiation and current smoking. Smoking behavior 3,497 European ancestry individuals 6,215 individuals, 1,648 twins Perlegen [427037] 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST000351 Genome-wide genotyping array 2009-06-16 19478329 Aston KI 2009-05-28 J Androl www.ncbi.nlm.nih.gov/pubmed/19478329 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. Male infertility 52 European ancestry oligozoospermic cases, 40 European ancestry non-obstructive azoospermic cases, 80 European ancestry controls NA Illumina [314776] 5 GCST000412 Genome-wide genotyping array 2009-04-01 19247474 Caporaso N 2009-02-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/19247474 Genome-wide and candidate gene association study of cigarette smoking behaviors. Smoking behavior 2,617 European ancestry smokers, 1,725 European ancestry controls NA Illumina [~ 518000] 21 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST000349 Genome-wide genotyping array 2010-04-15 20351715 Liu Y 2010-03-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20351715 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. Bipolar disorder or major depressive disorder 4,387 European and unknown ancestry bipolar disorder cases, 1,695 major depressive disorder cases, 7,970 European and unknown ancestry controls NA Affymetrix, Perlegen [1472580] (imputed) 9 unipolar depression, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985 GCST000641 Genome-wide genotyping array 2019-01-10 20351715 Liu Y 2010-03-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20351715 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. Bipolar disorder 4,387 European and unknown ancestry cases, 6,209 European and unknown ancestry controls NA Affymetrix [1769948] (imputed) 21 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST006865 Genome-wide genotyping array 2018-11-14 20351715 Liu Y 2010-03-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20351715 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. Major depressive disorder 1,695 cases, 1,761 controls NA Perlegen [1893617] (imputed) 3 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST006582 Genome-wide genotyping array 2012-03-10 22327514 Postel-Vinay S 2012-02-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22327514 Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma. Ewing sarcoma Up to 427 European ancestry cases, up to 4,352 European ancestry controls 661 European ancestry cases, 1,299 European ancestry controls NR [286966] 3 Ewing sarcoma http://www.ebi.ac.uk/efo/EFO_0000174 GCST001407 Genome-wide genotyping array 2012-06-19 22508271 Rasmussen-Torvik LJ 2012-04-16 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/22508271 Fasting glucose GWAS candidate region analysis across ethnic groups in the Multiethnic Study of Atherosclerosis (MESA). Fasting plasma glucose 2,349 European ancestry individuals, 664 Chinese ancestry individuals, 1,366 African American individuals, 1,171 Hispanic individuals NA Affymetrix [NR] (imputed) 3 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST001486 Genome-wide genotyping array 2013-09-26 23652523 Mayerle J 2013-05-08 JAMA www.ncbi.nlm.nih.gov/pubmed/23652523 Identification of genetic loci associated with Helicobacter pylori serologic status. Helicobacter pylori serologic status 2,623 European ancestry high titer cases, 7,862 European ancestry low or no titer controls NA Affymetrix, Illumina [~ 2500000] (imputed) 2 anti-Helicobacter pylori serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0005247 GCST002014 Genome-wide genotyping array 2012-06-18 22524403 Rice JP 2012-04-24 Addiction www.ncbi.nlm.nih.gov/pubmed/22524403 CHRNB3 is more strongly associated with Fagerström test for cigarette dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results. Nicotine dependence 2,267 European ancestry individuals, 99 Hispanic individuals, 999 African American individuals 835 individuals Illumina [948658] 1 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST001490 Genome-wide genotyping array 2012-04-06 22419738 Osman W 2012-03-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22419738 A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma. Glaucoma (primary open-angle) 1,394 Japanese ancestry cases, 6,599 Japanese ancestry controls 1,802 Japanese ancestry cases, 7,212 Japanese ancestry controls Illumina [602216] 3 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST001451 Genome-wide genotyping array 2010-05-26 20421487 Hodgkinson CA 2010-04-26 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/20421487 Genome-wide association identifies candidate genes that influence the human electroencephalogram. Electroencephalogram traits 322 Plains American Indian ancestry individuals 185 European ancestry individuals Illumina [405281] 0 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST000670 Genome-wide genotyping array 2009-11-12 19850125 Kim HJ 2009-10-19 Neurobiol Dis www.ncbi.nlm.nih.gov/pubmed/19850125 Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica. Neuromyelitis optica 53 Korean ancestry cases, 240 Korean ancestry controls 37 Korean ancestry cases Illumina [288025] 0 neuromyelitis optica http://www.ebi.ac.uk/efo/EFO_0004256 GCST000508 Genome-wide genotyping array 2012-03-17 22368281 Deshmukh HA 2012-02-24 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/22368281 Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a). Response to statin therapy 2,702 European ancestry individuals 2,550 European ancestry individuals Illumina, Perlegen [NR] (imputed) 1 response to statin http://purl.obolibrary.org/obo/GO_0036273 GCST001425 Genome-wide genotyping array 2013-02-27 23284291 Hancock DB 2012-12-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23284291 Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function. Pulmonary function (smoking interaction) 50,047 European ancestry individuals NA NR [~ 2500000] (imputed) 53 pulmonary function measurement, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0003892, http://www.ebi.ac.uk/efo/EFO_0005671 GCST001784 Genome-wide genotyping array 2012-08-08 22694956 Cipriani V 2012-06-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22694956 Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. Age-related macular degeneration 893 European ancestry cases, 2,199 European ancestry controls 1,411 European ancestry cases, 1,431 European ancestry controls Illumina [2272849] (imputed) 6 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST001571 Genome-wide genotyping array 2012-03-03 21732829 Dolmans GH 2011-07-06 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/21732829 Wnt signaling and Dupuytren's disease. Dupuytren's disease 856 European ancestry cases, 2,836 European ancestry controls 1,298 European ancestry cases, 7,136 European ancestry controls Illumina [234939] 12 Dupuytren Contracture http://www.ebi.ac.uk/efo/EFO_0004229 GCST001144 Genome-wide genotyping array 2011-09-30 21876539 Amin N 2011-08-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21876539 Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM. Coffee consumption 18,176 European ancestry individuals 7,929 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 4 coffee consumption http://www.ebi.ac.uk/efo/EFO_0004330 GCST001215 Genome-wide genotyping array 2011-10-04 21912186 Smith AK 2011-09-09 Neuropsychobiology www.ncbi.nlm.nih.gov/pubmed/21912186 Convergent genomic studies identify association of GRIK2 and NPAS2 with chronic fatigue syndrome. Chronic fatigue syndrome 40 European ancestry cases, 40 European ancestry controls NA Affymetrix [93508] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST001223 Genome-wide genotyping array 2012-05-16 22472174 Xiao Y 2012-04-03 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/22472174 SSBP2 variants are associated with survival in glioblastoma patients. Glioblastoma 315 European ancestry cases 434 European ancestry cases Illumina [314635] 1 glioblastoma multiforme http://www.ebi.ac.uk/efo/EFO_0000519 GCST001470 Genome-wide genotyping array 2012-04-28 22479309 Boraska V 2012-03-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/22479309 Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts. Brachial circumference 18,753 European ancestry individuals 3,623 European ancestry individuals Affymetrix, Illumina [2238430] (imputed) 1 brachial circumference http://www.ebi.ac.uk/efo/EFO_0004589 GCST001462 Genome-wide genotyping array 2012-07-31 22745009 Melville SA 2012-05-15 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/22745009 Multiple loci influencing hippocampal degeneration identified by genome scan. Hippocampal atrophy 1149 European ancestry Alzheimer disease cases, 336 European ancestry individuals with mild cognitive impairment, 188 European ancestry controls 419 African American Alzheimer disease cases Illumina [2131250] (imputed) 12 hippocampal atrophy http://www.ebi.ac.uk/efo/EFO_0005039 GCST001530 Genome-wide genotyping array 2011-10-16 21946350 Soler Artigas M 2011-09-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21946350 Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Pulmonary function 48,201 European ancestry individuals 46,411 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 18 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST001248 Genome-wide genotyping array 2011-10-18 21946350 Soler Artigas M 2011-09-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21946350 Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. Pulmonary function 48,201 European ancestry individuals 46,411 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 16 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST001251 Genome-wide genotyping array 2012-10-23 22889924 Scharf JM 2012-08-14 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22889924 Genome-wide association study of Tourette's syndrome. Tourette syndrome 778 European ancestry cases, 4,414 European ancestry controls, 242 Ashkenazi Jewish cases, 354 Ashkenazi Jewish controls, 265 French Canadian founder cases, 196 French Canadian founder controls 211 Latin American cases, 285 Latin American controls Illumina [484295] 7 Tourette syndrome http://www.ebi.ac.uk/efo/EFO_0004895 GCST001635 Genome-wide genotyping array 2011-09-27 21866343 Ahn MJ 2011-08-25 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21866343 The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations. Non-small cell lung cancer 445 Korean ancestry cases, 497 Korean ancestry controls 396 Korean ancestry cases, 998 Korean ancestry controls Affymetrix [474503] 1 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST001210 Genome-wide genotyping array 2015-04-23 19875614 Paterson AD 2009-10-29 Diabetes www.ncbi.nlm.nih.gov/pubmed/19875614 A genome-wide association study identifies a novel major locus for glycemic control in type 1 diabetes, as measured by both A1C and glucose. Glycemic control in type 1 diabetes (HbA1c) 667 European ancestry conventional treatment cases, 637 European ancestry intensive treatment cases 1,382 European ancestry cases Affymetrix, Illumina [2518578] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST000516 Genome-wide genotyping array 2010-03-05 20159242 Li X 2010-02-01 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/20159242 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. Asthma 607 European ancestry cases, 3,294 European ancestry controls NA Illumina [292443] 3 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000576 Genome-wide genotyping array 2013-02-27 23266558 Yamazaki K 2012-12-21 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/23266558 A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population. Crohn's disease 372 Japanese ancestry cases,3,389 Japanese ancestry controls Up to 1,151 Japanese ancestry cases, up to 15,800 Japanese ancestry controls Illumina [4929034] (imputed) 11 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST001785 Genome-wide genotyping array 2013-03-22 23269536 Sun J 2012-12-27 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23269536 Genome-wide association study identified novel genetic variant on SLC45A3 gene associated with serum levels prostate-specific antigen (PSA) in a Chinese population. Prostate-specific antigen levels 1,999 Chinese ancestry males 1,496 Chinese ancestry males Illumina [> 709211] (imputed) 3 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST001796 Genome-wide genotyping array 2012-09-11 22764253 Thier S 2012-07-03 Neurology www.ncbi.nlm.nih.gov/pubmed/22764253 Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor. Essential tremor 436 European ancestry cases, 928 European ancestry controls 554 European ancestry cases, 609 European ancestry controls Affymetrix [620077] 1 essential tremor http://www.ebi.ac.uk/efo/EFO_0003108 GCST001590 Genome-wide genotyping array 2013-05-01 23382809 Xu C 2013-01-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/23382809 BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies. Schizophrenia (negative symptoms) 1,774 European ancestry cases, 2,726 European ancestry controls Affymetrix [729454] 3 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001836 Genome-wide genotyping array 2013-05-09 23377640 GENDEP Investigators 2013-02-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/23377640 Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies. Major depressive disorder Up to 2,256 European ancestry cases NA Affymetrix, Illumina [1200000] (imputed) 49 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST001850 Genome-wide genotyping array 2011-04-06 21383967 Zhernakova A 2011-02-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21383967 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. Celiac disease or Rheumatoid arthritis 4,533 European ancestry celiac disease cases, 5,539 European ancestry rheumatoid arthritis cases, 27,981 European ancestry controls 2,169 European ancestry celiac disease cases, 2,845 European ancestry rheumatoid arthritis cases, 7,199 European ancestry controls Illumina [472854] 15 immune system disease http://www.ebi.ac.uk/efo/EFO_0000540 GCST000987 Genome-wide genotyping array 2013-06-21 23470693 Zeng Z 2013-03-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/23470693 Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition. Pit-and-Fissure caries 996 European ancestry individuals Illumina [1200000] (imputed) 8 pit and fissure surface dental caries http://www.ebi.ac.uk/efo/EFO_0006338 GCST001897 Genome-wide genotyping array 2013-06-21 23470693 Zeng Z 2013-03-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/23470693 Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition. Smooth-surface caries 982 European ancestry individuals NA Illumina [1200000] (imputed) 11 smooth surface dental caries http://www.ebi.ac.uk/efo/EFO_0006339 GCST001896 Genome-wide genotyping array 2009-05-07 19389651 Smith JG 2009-02-15 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/19389651 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. Electrocardiographic conduction measures 1,262 Kosraen individuals NA Affymetrix [338049] 7 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST000344 Genome-wide genotyping array 2008-09-03 18591461 Turner ST 2008-06-30 Hypertension www.ncbi.nlm.nih.gov/pubmed/18591461 Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic. Response to diuretic therapy 97 African American good response individuals, 97 African American poor response individuals, 98 European ancestry good response individuals, 97 European ancestry poor response individuals NA Affymetrix [up to 102334] 1 response to diuretic http://purl.obolibrary.org/obo/GO_0036270 GCST000208 Genome-wide genotyping array 2008-06-16 18372905 Tomlinson IP 2008-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18372905 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. Colorectal cancer 922 European ancestry cases, 927 European ancestry controls 17,089 European ancestry cases, 16,862 European ancestry controls, 783 cases, 664 controls Illumina [547647] 5 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000169 Genome-wide genotyping array 2013-03-20 23381943 Williams FM 2013-01-01 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/23381943 Ischemic stroke is associated with the ABO locus: the EuroCLOT study. End-stage coagulation 2,100 European ancestry individuals NA Illumina [NR] (imputed) 23 factor VIII measurement, von Willebrand factor measurement, coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0004629, http://www.ebi.ac.uk/efo/EFO_0004634 GCST001798 Genome-wide genotyping array 2009-09-11 19684603 Trevino LR 2009-08-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19684603 Germline genomic variants associated with childhood acute lymphoblastic leukemia. Acute lymphoblastic leukemia (childhood) 317 European ancestry cases, 17,958 European ancestry controls NA Affymetrix [307944] 14 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST000464 Genome-wide genotyping array 2013-11-20 23720494 Evans DM 2013-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23720494 Genome-wide association study identifies loci affecting blood copper, selenium and zinc. Blood trace element (Se levels) 5477 European ancestry individuals NA Illumina [> 2500000] (imputed) 10 serum selenium measurement http://www.ebi.ac.uk/efo/EFO_0005266 GCST002039 Genome-wide genotyping array 2013-11-20 23720494 Evans DM 2013-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23720494 Genome-wide association study identifies loci affecting blood copper, selenium and zinc. Blood trace element (Cu levels) 2,603 European ancestry individuals NA Illumina [> 2500000] (imputed) 7 serum copper measurement http://www.ebi.ac.uk/efo/EFO_0005267 GCST002041 Genome-wide genotyping array 2013-11-20 23720494 Evans DM 2013-05-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23720494 Genome-wide association study identifies loci affecting blood copper, selenium and zinc. Blood trace element (Zn levels) 2,603 European ancestry individuals NA Illumina [> 2500000] (imputed) 11 serum zinc measurement http://www.ebi.ac.uk/efo/EFO_0005268 GCST002040 Genome-wide genotyping array 2008-09-03 18846228 Weidinger S 2008-08-22 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/18846228 Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. IgE levels 1,530 European ancesrty individuals 9,769 European ancestry individuals Affymetrix [353569] 2 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST000222 Genome-wide genotyping array 2008-06-16 17463246 Saxena R 2007-04-26 Science www.ncbi.nlm.nih.gov/pubmed/17463246 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Type 2 diabetes 1,464 European ancestry cases, 1,467 European ancestry controls 5,065 European ancestry cases, 5,785 European ancestry controls, at least 18,129 cases and controls. Affymetrix [386731] 8 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000028 Genome-wide genotyping array 2009-02-13 17463246 Saxena R 2007-04-26 Science www.ncbi.nlm.nih.gov/pubmed/17463246 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Triglycerides 2,659 European ancestry type 2 diabetes cases and controls 5,217 European ancestry individuals Affymetrix [389878] 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000026 Genome-wide genotyping array 2017-11-01 17463246 Saxena R 2007-04-26 Science www.ncbi.nlm.nih.gov/pubmed/17463246 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. HDL cholesterol levels 2,623 European ancestry type 2 diabetes cases and controls NA Affymetrix [389878] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST004919 Genome-wide genotyping array 2017-11-01 17463246 Saxena R 2007-04-26 Science www.ncbi.nlm.nih.gov/pubmed/17463246 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. LDL cholesterol levels 2,601 European ancestry type 2 diabetes cases and controls NA Affymetrix [389878] 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST004920 Genome-wide genotyping array 2017-11-01 17463246 Saxena R 2007-04-26 Science www.ncbi.nlm.nih.gov/pubmed/17463246 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Apolipoprotein A1 levels 1,451 European ancestry type 2 diabetes cases and controls NA Affymetrix [389878] 1 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST004921 Genome-wide genotyping array 2009-09-29 19734900 Rung J 2009-09-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19734900 Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia. Type 2 diabetes 679 European ancestry cases, 697 European ancestry controls 5,579 European ancestry cases, 7,096 European ancestry controls Illumina [392365] 6 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000478 Genome-wide genotyping array 2009-06-22 19503597 Kolz M 2009-06-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19503597 Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations. Uric acid levels 12,328 European ancestry males, 15,813 European ancestry females NA Affymetrix, Illumina [2493963] (imputed) 11 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST000418 Genome-wide genotyping array 2012-01-06 22159054 Logue MW 2011-12-01 Arch Neurol www.ncbi.nlm.nih.gov/pubmed/22159054 A comprehensive genetic association study of Alzheimer disease in African Americans. Alzheimer's disease 513 African American cases, 496 African American controls NA Illumina [2505093] (imputed) 11 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001342 Genome-wide genotyping array 2012-01-17 22190364 Patsopoulos NA 2011-12-01 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/22190364 Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Multiple sclerosis 5,545 European ancestry cases, 12,153 European ancestry controls NA Affymetrix, Illumina [2529394] 19 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST001341 Genome-wide genotyping array 2009-09-10 19723657 Spain SL 2009-09-01 Cancer Res www.ncbi.nlm.nih.gov/pubmed/19723657 Colorectal cancer risk is not associated with increased levels of homozygosity in a population from the United Kingdom. Colorectal cancer 921 European ancestry cases, 929 European ancestry controls 1,214 European ancestry cases, 1,435 European ancestry controls Illumina [486303] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000472 Genome-wide genotyping array 2009-02-27 19116933 Hinks A 2009-01-01 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/19116933 Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. Arthritis (juvenile idiopathic) 279 European ancestry cases, 184 European ancestry controls up to 654 European ancestry cases, 2,024 European ancestry controls Affymetrix [88862] 1 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST000309 Genome-wide genotyping array 2013-11-15 23708190 Hu Z 2013-05-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23708190 A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations. Congenital heart malformation 945 Han Chinese ancestry cases, 1,246 Han Chinese ancestry controls 2,160 Han Chinese ancestry cases, 3,866 Han Chinese ancestry controls Illumina [708275] 2 congenital heart malformation http://www.ebi.ac.uk/efo/EFO_0005269 GCST002036 Genome-wide genotyping array 2012-01-19 22205951 Kerner B 2011-12-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/22205951 Genome-wide association study in bipolar patients stratified by co-morbidity. Bipolar disorder 1,000 European ancestry cases, 1,034 European ancestry controls NA Affymetrix [728331] 3 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001359 Genome-wide genotyping array 2010-09-22 20713499 Huang J 2010-08-16 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/20713499 Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression. Schizophrenia, bipolar disorder and depression (combined) 402 European ancestry schizophrenia cases, 1,021 European ancestry bipolar I cases, 493 European ancestry bipolar II cases, 1,210 European ancestry MDD cases, 1,060 European ancestry controls NA Affymetrix, Perlegen [1574154] (imputed) 5 unipolar depression, bipolar disorder, mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0000677 GCST000774 Genome-wide genotyping array 2011-07-20 21658281 Aouizerat BE 2011-06-10 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/21658281 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. Sudden cardiac arrest 88 European ancestry cases, 517 European ancestry controls NA Affymetrix [319222] 6 sudden cardiac arrest http://www.ebi.ac.uk/efo/EFO_0004278 GCST001102 Genome-wide genotyping array 2011-07-20 21658281 Aouizerat BE 2011-06-10 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/21658281 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. Sudden cardiac arrest 88 European ancestry cases, 517 European ancestry controls NA Affymetrix [319222] 7 sudden cardiac arrest http://www.ebi.ac.uk/efo/EFO_0004278 GCST001104 Genome-wide genotyping array 2011-07-20 21658281 Aouizerat BE 2011-06-10 BMC Cardiovasc Disord www.ncbi.nlm.nih.gov/pubmed/21658281 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. Sudden cardiac arrest 88 European ancestry cases, 517 European ancestry controls NA Affymetrix [319222] 36 sudden cardiac arrest http://www.ebi.ac.uk/efo/EFO_0004278 GCST001099 Genome-wide genotyping array 2009-09-30 19749758 Suppiah V 2009-09-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19749758 IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. Response to hepatitis C treatment 131 European ancestry responders, 162 European ancestry non-responders 261 European ancestry responders, 294 European ancestry non-responders Illumina [311159] 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST000485 Genome-wide genotyping array 2011-01-06 21084426 Saad M 2010-11-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21084426 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. Parkinson's disease 1,039 European ancestry cases, 1,984 European ancestry controls 3,232 European ancestry cases, 7,064 European ancestry controls Illumina [492929] 3 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000874 Genome-wide genotyping array 2010-10-05 20826269 Panicker V 2010-09-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20826269 A locus on chromosome 1p36 is associated with thyrotropin and thyroid function as identified by genome-wide association study. Thyroid function 2,014 European ancestry twins 1,093 European ancestry individuals Illumina [2120505] 0 thyroid function http://www.ebi.ac.uk/efo/EFO_0004296 GCST000791 Genome-wide genotyping array 2010-08-18 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Platelet count 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 1 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST000510 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Basophil count 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST008427 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Eosinophil counts 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST008428 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Hemoglobin levels 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST008429 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Hematocrit 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST008430 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Lymphocyte count 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST008431 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Mean corpuscular hemoglobin 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 3 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST008432 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Mean corpuscular hemoglobin concentration 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST008418 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Mean corpuscular volume 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 2 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST008420 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Monocyte count 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST008421 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Neutrophil count 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST008425 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. Red blood cell count 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST008426 Genome-wide genotyping array 2019-08-13 19853236 Ferreira MA 2009-10-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19853236 Sequence variants in three loci influence monocyte counts and erythrocyte volume. White blood cell count 2,538 European ancestry individuals, 3,477 individuals 1,543 individuals Illumina, Perlegen [~ 2500000] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST008419 Genome-wide genotyping array 2011-12-20 22116939 Guo Y 2011-11-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22116939 Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. Epilepsy 504 Han Chinese ancestry cases, 2,947 Han Chinese ancestry controls 583 Han Chinese ancestry cases, 497 Han Chinese ancestry controls Illumina [461024] 1 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST001329 Genome-wide genotyping array 2010-10-05 20835238 Thorleifsson G 2010-09-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20835238 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. Glaucoma (primary open-angle) 1,263 European ancestry cases, 34,887 European ancestry controls 2,175 European ancestry cases, 2,064 European ancestry controls Illumina [303117] 1 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST000793 Genome-wide genotyping array 2010-09-23 20801718 Laaksovirta H 2010-08-27 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/20801718 Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. Amyotrophic lateral sclerosis 405 European ancestry cases, 497 European ancestry controls NA Illumina [318167] 2 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000781 Genome-wide genotyping array 2011-06-18 21647738 Wu Y 2011-06-07 Inflammation www.ncbi.nlm.nih.gov/pubmed/21647738 Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment. C-reactive protein 1,709 Filipino ancestry female individuals NA Affymetrix [2073674] (imputed) 3 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST001093 Genome-wide genotyping array 2010-01-28 20072603 Guo Y 2010-01-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20072603 Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. Osteoporosis 350 Han Chinese ancestry cases, 350 Han Chinese ancestry controls 390 Han Chinese ancestry cases, 516 Han Chinese ancestry controls Affymetrix [281533] 1 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST000560 Genome-wide genotyping array 2010-01-21 20060832 Rauch A 2010-01-07 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/20060832 Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. Chronic hepatitis C infection 1,015 European ancestry chronic HCV carriers, 347 European ancestry spontaneously cleared HCV individuals NA Illumina [~ 500000] 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST000557 Genome-wide genotyping array 2010-09-11 20676098 Takata R 2010-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20676098 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. Prostate cancer 1,583 Japanese ancestry cases, 3,386 Japanese ancestry controls 3,001 Japanese ancestry cases, 5,415 Japanese ancestry controls Illumina [510687] 11 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000750 Genome-wide genotyping array 2009-09-28 19727025 De Moor MH 2009-09-02 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/19727025 Genome-wide association study of exercise behavior in Dutch and American adults. Leisure-time exercise behaviour 2,622 European ancestry individuals NA Affymetrix, Perlegen [~ 1600000] (imputed) 3 exercise http://www.ebi.ac.uk/efo/EFO_0000483 GCST000474 Genome-wide genotyping array 2012-11-08 19734545 Need AC 2009-09-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19734545 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. Cognitive performance Up to 1,295 individuals NA Illumina [475971] 59 neuropsychological test http://www.ebi.ac.uk/efo/EFO_0003926 GCST000477 Genome-wide genotyping array 2011-05-24 21490949 Sim X 2011-04-07 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21490949 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. Type 2 diabetes 2,010 Chinese ancestry cases, 1,945 Chinese ancestry controls, 794 Malay ancestry cases, 1,240 Malay ancestry controls, 977 Asian Indian ancestry cases, 1,169 Asian Indian ancestry controls NA Illumina [~ 2000000] (imputed) 17 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001033 Genome-wide genotyping array 2010-07-12 20570966 McGovern DP 2010-06-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20570966 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. Crohn's disease 896 European ancestry cases, 3,204 European ancestry controls 1,174 European ancestry cases, 357 European ancestry controls Illumina [304825] 7 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000705 Genome-wide genotyping array 2010-09-17 20802479 Anttila V 2010-08-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20802479 Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Migraine 2,731 European ancestry cases, 10,747 European ancestry controls 3,202 European ancestry cases, 40,062 European ancestry controls Illumina [429912] 1 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST000782 Genome-wide genotyping array 2010-12-01 20953189 Stuart PE 2010-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20953189 Genome-wide association analysis identifies three psoriasis susceptibility loci. Psoriasis Up to 1,831 cases, up to 2,546 controls Up to 4,064 cases, up to 4,685 controls Illumina, Perlegen [up to 7456344] (imputed) 8 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST000834 Genome-wide genotyping array 2011-06-23 21627779 Antunez C 2011-05-31 Genome Med www.ncbi.nlm.nih.gov/pubmed/21627779 The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease. Alzheimer's disease 319 European ancestry cases, 769 European ancestry controls, 2,690 cases, 2,237 controls 4,982 European ancestry cases, 7,961 European ancestry controls, 2,190 cases, 3,374 controls Affymetrix, Illumina [696707] (imputed) 5 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001087 Genome-wide genotyping array 2011-01-11 21139019 Walsh KM 2010-12-07 Endocr Relat Cancer www.ncbi.nlm.nih.gov/pubmed/21139019 A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. Ileal carcinoids 239 European ancestry cases, 107 European ancestry controls NA Illumina [308330] 4 carcinoid tumor http://www.ebi.ac.uk/efo/EFO_0004243 GCST000908 Genome-wide genotyping array 2011-01-08 21113153 van der Zanden LF 2010-11-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21113153 Common variants in DGKK are strongly associated with risk of hypospadias. Hypospadias 436 European ancestry cases, 494 European ancestry controls 133 European ancestry cases and their parents, 266 European ancestry cases, 402 European ancestry controls Affymetrix [574400] 1 hypospadias http://www.ebi.ac.uk/efo/EFO_0004209 GCST000888 Genome-wide genotyping array 2010-10-15 20876420 Ingle JN 2010-09-27 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/20876420 Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors. Adverse response to aromatase inhibitors 293 cases, 585 controls NA Illumina [551395] 1 response to aromatase inhibitor http://purl.obolibrary.org/obo/GO_0061477 GCST000813 Genome-wide genotyping array 2012-01-04 22138694 Lin Z 2011-12-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22138694 A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis. Ankylosing spondylitis 1,837 Han Chinese ancestry cases, 4,231 Han Chinese ancestry controls 2,100 Han Chinese ancestry cases, 3,496 Han Chinese ancestry controls Illumina [1356350] (imputed) 5 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST001345 Genome-wide genotyping array 2009-07-01 19557197 Heard-Costa NL 2009-06-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19557197 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. Waist circumference 31,373 European ancestry individuals 38,641 individuals Affymetrix, Illumina [up to 512349] 7 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST000427 Genome-wide genotyping array 2008-06-18 18471798 Valdes AM 2008-05-08 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18471798 Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis. Knee osteoarthritis 357 European ancestry cases, 285 European ancestry controls 1,177 European ancestry cases, 2,372 European ancestry controls Illumina [413461] 2 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST000186 Genome-wide genotyping array 2010-10-15 20872241 Li J 2010-09-26 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/20872241 A combined analysis of genome-wide association studies in breast cancer. Breast cancer 2,702 European ancestry female cases, 5,726 European ancestry controls Up to 7,386 cases, 7,576 controls Illumina [285984] 4 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000811 Genome-wide genotyping array 2008-06-22 18464913 Melzer D 2008-05-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/18464913 A genome-wide association study identifies protein quantitative trait loci (pQTLs). Protein quantitative trait loci 1,200 European ancestry individuals up to 4,590 European ancestry individuals Illumina [496032] 49 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST000189 Genome-wide genotyping array 2013-05-31 23449627 Cousminer DL 2013-02-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23449627 Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Pubertal anthropometrics up to 5,043 European ancestry males, up to 5,756 European ancestry females NA Affymetrix, Illumina [~ 2500000] (imputed) 14 puberty, height growth measurement http://www.ebi.ac.uk/efo/EFO_0001382, http://www.ebi.ac.uk/efo/EFO_0005201 GCST001876 Genome-wide genotyping array 2013-05-31 23449627 Cousminer DL 2013-02-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23449627 Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Pubertal anthropometrics 7,161 European ancestry males, 6,879 European ancestry females 5,133 European ancestry males, 4,577 European ancestry females Affymetrix, Illumina [~ 2500000] (imputed) 11 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST001875 Genome-wide genotyping array 2008-06-22 18463370 Maris JM 2008-05-09 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/18463370 Chromosome 6p22 locus associated with clinically aggressive neuroblastoma. Neuroblastoma 1,032 European ancestry cases, 2,043 European ancestry controls 720 European ancestry cases, 2,128 European ancestry controls Illumina [464934] 1 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST000188 Genome-wide genotyping array 2008-08-07 18615156 Liu C 2008-07-10 Mol Med www.ncbi.nlm.nih.gov/pubmed/18615156 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. Response to TNF antagonist treatment 89 European ancestry cases NA Illumina [283348] 8 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST000211 Genome-wide genotyping array 2008-12-09 18846501 Sonuga-Barke EJ 2008-10-07 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18846501 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. Attention deficit hyperactivity disorder symptoms (maternal expressed emotions interaction) 909 European ancestry trios NA Perlegen [429981] 7 attention deficit hyperactivity disorder, parental emotion expression measurmement http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0008342 GCST000247 Genome-wide genotyping array 2009-01-15 18846501 Sonuga-Barke EJ 2008-10-07 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18846501 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. Conduct disorder (maternal expressed emotions interaction) 909 European ancestry trios NA Perlegen [429901] 15 parental emotion expression measurmement, conduct disorder http://www.ebi.ac.uk/efo/EFO_0008342, http://www.ebi.ac.uk/efo/EFO_0004216 GCST000245 Genome-wide genotyping array 2012-01-27 22199011 Murabito JM 2011-12-23 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/22199011 Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Ankle-brachial index 38,376 European ancestry individuals, 2,133 Erasmus Rucphen individuals, 1,183 Old Order Amish individuals 16,717 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 2 ankle brachial index http://www.ebi.ac.uk/efo/EFO_0003912 GCST001361 Genome-wide genotyping array 2008-12-09 18991354 Gretarsdottir S 2008-10-01 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/18991354 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. Stroke (ischemic) 1,661 European ancestry cases, 10,815 European ancestry controls 4,576 European ancestry cases, 19,343 European ancestry controls Illumina [310881] 1 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST000239 Genome-wide genotyping array 2011-12-01 22036096 Ramasamy A 2011-11-01 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/22036096 A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. IgE grass sensitization 2,315 European ancestry cases, 10,032 European ancestry controls NA Affymetrix, Illumina [2217510] (imputed) 9 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST001303 Genome-wide genotyping array 2011-12-01 22036096 Ramasamy A 2011-11-01 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/22036096 A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order. Allergic rhinitis 3,933 European ancestry cases, 8,965 European ancestry controls NA Affymetrix, Illumina [2217510] (imputed) 9 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST001310 Genome-wide genotyping array 2011-02-16 21155030 Cheong MY 2011-01-11 Yonsei Med J www.ncbi.nlm.nih.gov/pubmed/21155030 Association of the adiponectin gene variations with risk of ischemic stroke in a Korean population. Stroke (ischemic) 160 Korean ancestry cases, 160 Korean ancestry controls 673 Korean ancestry cases, 267 Korean ancestry controls Affymetrix [~ 320250] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST000941 Genome-wide genotyping array 2008-12-09 18951430 Anney RJ 2008-10-24 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18951430 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. Attention deficit hyperactivity disorder and conduct disorder 938 European ancestry trios NA Perlegen [378332] 26 attention deficit hyperactivity disorder, conduct disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004216 GCST000253 Genome-wide genotyping array 2008-08-27 19165918 Graham RR 2008-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19165918 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. Systemic lupus erythematosus 431 European ancestry cases, 2,155 European ancestry controls 447 European ancestry trios, 293 trios Affymetrix [313238] 8 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000216 Genome-wide genotyping array 2008-07-30 18604267 Pare G 2008-07-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/18604267 Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women. Soluble ICAM-1 4,570 European ancestry female individuals 2,008 European ancestry female individuals Illumina [336108] 4 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST000210 Genome-wide genotyping array 2009-05-21 19421330 Yang HC 2009-05-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/19421330 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. Hypertension (young onset) 175 Han Chinese ancestry cases, 175 Han Chinese ancestry controls 833 Han Chinese ancestry cases, 833 Han Chinese ancestry controls Affymetrix [91713] 1 early onset hypertension http://www.ebi.ac.uk/efo/EFO_0004772 GCST000390 Genome-wide genotyping array 2009-05-21 19430760 Rich SS 2009-05-09 Diabetologia www.ncbi.nlm.nih.gov/pubmed/19430760 A genome-wide association scan for acute insulin response to glucose in Hispanic-Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS FS). Insulin resistance/response 229 Hispanic individuals from 34 families 961 Hispanic family members Illumina [309200] 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST000391 Genome-wide genotyping array 2009-06-14 19465909 Jallow M 2009-05-24 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19465909 Genome-wide and fine-resolution association analysis of malaria in West Africa. Malaria 958 Gambian ancestry cases, 1,382 Gambian ancestry controls 1,087 Gambian ancestry cases, 2,376 Gambian ancestry controls Affymetrix [402814] 3 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST000410 Genome-wide genotyping array 2009-06-10 19456320 Ma D 2009-05-28 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/19456320 A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Autism 1,390 European ancestry individuals from 438 families 2,390 European ancestry individuals from 457 families Illumina [775311] 1 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST000411 Genome-wide genotyping array 2008-12-11 18227835 Berrettini W 2008-01-29 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/18227835 Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking. Nicotine dependence 7,481 European ancestry individuals ~2000 European ancestry individuals Affymetrix [460959] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST000147 Genome-wide genotyping array 2008-12-09 18987618 Cronin S 2008-11-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18987618 Screening for replication of genome-wide SNP associations in sporadic ALS. Amyotrophic lateral sclerosis 958 European ancestry cases, 932 European ancestry controls 309 European ancestry cases, 404 European ancestry controls Illumina [287522] 1 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000260 Genome-wide genotyping array 2010-09-23 20719862 Vitart V 2010-08-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20719862 New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8. Central corneal thickness 1,445 European ancestry individuals 5,882 European ancestry individuals Illumina [~ 2000000] (imputed) 5 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST000775 Genome-wide genotyping array 2013-08-16 20014019 Dubinsky MC 2010-08-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/20014019 Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease. Response to anti-TNF alpha therapy in inflammatory bowel disease 94 pediatric cases NA Illumina [301742] 4 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST000748 Genome-wide genotyping array 2011-01-03 21041692 Denny JC 2010-11-01 Circulation www.ncbi.nlm.nih.gov/pubmed/21041692 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. Atrioventricular conduction 2,334 European ancestry individuals NA Illumina [514999] 5 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST000852 Genome-wide genotyping array 2009-03-31 19193627 Chio A 2009-02-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19193627 A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 537 European ancestry cases, 1,984 European ancestry controls 2,741 European ancestry cases, 2,875 European ancestry controls Illumina [545066] 0 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000333 Genome-wide genotyping array 2008-10-14 18820697 Miyagawa T 2008-09-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18820697 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. Narcolepsy 222 Japanese ancestry cases, 389 Japanese ancestry controls 274 East Asian ancestry cases, 499 East Asian ancestry controls, 388 European ancestry cases, 397 European ancestry controls, 86 African American cases, 98 African American controls Affymetrix [249133] 1 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST000236 Genome-wide genotyping array 2008-09-17 18327257 Vitart V 2008-03-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18327257 SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout. Urate levels 794 European ancestry individuals 706 European ancestry individuals Illumina [308140] 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST000160 Genome-wide genotyping array 2010-09-07 20661308 Kapur K 2010-07-22 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20661308 Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene. Calcium levels 8,918 European ancestry individuals, 3,947 Indian Asian ancestry individuals 4,126 European ancestry individuals Affymetrix, Illumina, Perlegen [2557252] (imputed) 1 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST000736 Genome-wide genotyping array 2015-05-23 21300955 Dehghan A 2011-02-07 Circulation www.ncbi.nlm.nih.gov/pubmed/21300955 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. C-reactive protein levels 63,678 European ancestry individuals 1,792 Erasmus Rucphen individuals, 715 Orcadian individuals 16,540 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 20 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST000965 Genome-wide genotyping array 2008-08-07 18723019 Franke A 2008-07-21 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/18723019 Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2. Crohn's disease and sarcoidosis (combined) 382 European ancestry Crohn's disease cases, 398 European ancestry Sarcoidosis cases, 394 European ancestry controls 660 European ancestry Crohn's disease cases, 657 European ancestry Sarcoidosis cases, 1,091 European ancestry controls Affymetrix [83360] 1 sarcoidosis, Crohn's disease http://purl.obolibrary.org/obo/MONDO_0019338, http://www.ebi.ac.uk/efo/EFO_0000384 GCST000212 Genome-wide genotyping array 2008-06-27 18364390 Capon F 2008-03-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/18364390 Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene. Psoriasis 318 European ancestry cases, 288 European ancestry controls 2,361 European ancestry cases, 1,927 European ancestry controls Illumina [~ 408000] 2 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST000165 Genome-wide genotyping array 2008-06-20 18445777 Styrkarsdottir U 2008-04-29 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/18445777 Multiple genetic loci for bone mineral density and fractures. Bone mineral density (hip) 5,861 European ancestry individuals 7,925 European ancestry individuals Illumina [301019] 6 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000181 Genome-wide genotyping array 2008-06-20 18445777 Styrkarsdottir U 2008-04-29 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/18445777 Multiple genetic loci for bone mineral density and fractures. Bone mineral density (spine) 5,861 European ancestry individuals 7,925 European ancestry individuals Illumina [301019] 8 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000180 Genome-wide genotyping array 2010-09-22 20711176 Nakashima M 2010-08-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20711176 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. Keloid 178 Japanese ancestry cases, 906 Japanese ancestry controls 621 Japanese ancestry cases, 2,271 Japanese ancestry controls Illumina [452038] 4 Keloid http://www.ebi.ac.uk/efo/EFO_0004212 GCST000773 Genome-wide genotyping array 2008-09-25 18794853 Raychaudhuri S 2008-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18794853 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Rheumatoid arthritis 3,393 European ancestry cases, 12,460 European ancestry controls 3,929 European ancestry cases, 5,807 European ancestry controls Affymetrix, Illumina [at least 315971] (imputed) 9 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000232 Genome-wide genotyping array 2011-10-16 21940970 Meschia JF 2011-09-22 Stroke www.ncbi.nlm.nih.gov/pubmed/21940970 Siblings with ischemic stroke study: results of a genome-wide scan for stroke loci. Stroke 223 cases, 248 stroke-affected siblings, 84 stroke-unaffected siblings NA Illumina [NR] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST001246 Genome-wide genotyping array 2013-04-18 23349225 Hwang JY 2013-01-24 J Med Genet www.ncbi.nlm.nih.gov/pubmed/23349225 Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture. Osteoporosis 288 Korean ancestry cases, 1,139 Korean ancestry controls 831 East Asian ancestry cases, 2305 East Asian ancestry controls Affymetrix [1573409] (imputed) 1 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST001830 Genome-wide genotyping array 2008-06-16 17632509 Buch S 2007-07-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17632509 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. Gallstone disease 280 European ancestry cases, 360 European ancestry controls 1,833 European ancestry cases, 1,035 European ancestry controls, 167 Hispanic cases, 167 Hispanic controls Affymetrix [382492] 1 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST000055 Genome-wide genotyping array 2012-02-09 22247754 Murray SS 2012-01-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/22247754 Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias. Life threatening arrhythmia 607 European ancestry cases, 297 European ancestry controls NA Illumina [NR] (imputed) 2 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST001376 Genome-wide genotyping array 2011-10-20 21943158 Middelberg RP 2011-09-24 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/21943158 Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits. Cardiovascular disease risk factors 11,683 European ancestry individuals NA Illumina [NR] (imputed) 19 aspartate aminotransferase measurement, butyrylcholinesterase measurement, triglyceride measurement, ferritin measurement, serum gamma-glutamyl transferase measurement, low density lipoprotein cholesterol measurement, C-reactive protein measurement, uric acid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004736, http://www.ebi.ac.uk/efo/EFO_0004571, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004459, http://www.ebi.ac.uk/efo/EFO_0004532, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0004761, http://www.ebi.ac.uk/efo/EFO_0004612 GCST001247 Genome-wide genotyping array 2013-01-16 23114982 Siegert S 2012-11-02 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23114982 Genome-wide investigation of gene-environment interactions in colorectal cancer. Colorectal cancer (environment interaction) 314 European ancestry cases 259 European ancestry cases, 1,002 European ancestry controls Affymetrix [4373163] (imputed) 0 smoking status measurement, colorectal cancer, alcohol consumption measurement, overweight body mass index status http://www.ebi.ac.uk/efo/EFO_0006527, http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0005935 GCST001731 Genome-wide genotyping array 2013-06-21 23502781 Germain M 2013-03-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23502781 Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension. Pulmonary arterial hypertension (without BMPR2 mutations) 340 European ancestry cases, 1,068 European ancestry controls 285 cases, 457 controls Illumina [462499] 1 pulmonary arterial hypertension http://www.ebi.ac.uk/efo/EFO_0001361 GCST001908 Genome-wide genotyping array 2011-01-14 21059979 Shen H 2010-11-08 Arch Intern Med www.ncbi.nlm.nih.gov/pubmed/21059979 Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. LDL cholesterol 841 Amish individuals 663 Amish inidividuals Affymetrix [369241] 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000866 Genome-wide genotyping array 2009-09-04 19667218 Comabella M 2009-08-01 Arch Neurol www.ncbi.nlm.nih.gov/pubmed/19667218 Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis. Response to interferon beta therapy 53 responders, 53 non-responders 49 responders, 45 non-responders Affymetrix [428867] 0 response to interferon-beta http://purl.obolibrary.org/obo/GO_0035456 GCST000453 Genome-wide genotyping array 2011-10-21 21947420 Lei SF 2011-09-25 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21947420 Genome-wide association study identifies HMGN3 locus for spine bone size variation in Chinese. Spine bone size 1,627 Han Chinese ancestry individuals 1,728 European ancestry female individuals Affymetrix [689368] 0 spine bone size http://www.ebi.ac.uk/efo/EFO_0004508 GCST001249 Genome-wide genotyping array 2013-06-18 23536807 Scheetz TE 2013-03-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/23536807 A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci. Age-related macular degeneration 200 cases, 197 controls 200 cases, 200 controls Affymetrix [500000] 2 age-related macular degeneration, glaucoma http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0005041 GCST001899 Genome-wide genotyping array 2009-09-04 19651812 Chambers JC 2009-08-03 Diabetes www.ncbi.nlm.nih.gov/pubmed/19651812 Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians. Fasting plasma glucose 698 Asian Indian ancestry cases, 6,776 Asian Indian ancestry controls 4,462 European ancestry controls Illumina [up to 544390] 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000457 Genome-wide genotyping array 2008-09-17 18252221 Kayser M 2008-01-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18252221 Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene. Iris color 925 Erasmus Rucphen individuals, 481 European ancestry females 5,575 European ancestry individuals, 1,292 Erasmus Rucphen individuals Affymetrix, Illumina [up to 500000] 1 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST000146 Genome-wide genotyping array 2012-07-24 22673963 Lasky-Su J 2012-06-07 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22673963 Genome-wide association analysis of circulating vitamin D levels in children with asthma. Vitamin D levels 422 European ancestry trios with asthmatic children, 150 European ancestry asthmatic child cases 1,108 Hispanic asthmatic child cases Illumina [547645] 1 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST001560 Genome-wide genotyping array 2009-09-29 19734903 Lambert JC 2009-09-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19734903 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. Alzheimer's disease 2,032 European ancestry cases, 5,328 European ancestry controls 3,978 European ancestry cases, 3,297 European ancestry controls Illumina [537029] 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000480 Genome-wide genotyping array 2013-11-01 23583980 Fingerlin TE 2013-04-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23583980 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. Interstitial lung disease 1,161 European ancestry cases, 4,683 European ancestry controls 876 European ancestry cases, 1,890 European ancestry controls Illumina [439828] 16 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST001968 Genome-wide genotyping array 2009-07-30 19597491 Gudbjartsson DF 2009-07-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19597491 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. Atrial fibrillation 2,385 European ancestry cases, 33,752 European ancestry controls up to 2,427 European ancestry cases, 3,379 European ancestry controls, 286 Han Chinese ancestry cases, 2,763 Han Chinese ancestry controls Illumina [303136] 2 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST000446 Genome-wide genotyping array 2013-06-18 23561647 van Setten J 2013-03-13 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/23561647 Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction. Coronary artery calcification 2,620 European ancestry males NA Illumina [2500000] (imputed) 2 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST001902 Genome-wide genotyping array 2011-01-18 20953190 Strange A 2010-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20953190 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. Psoriasis 2,178 European ancestry cases, 5,175 European ancestry controls 3,174 European ancestry cases, 5,464 European ancestry controls Illumina [535475] 17 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST000833 Genome-wide genotyping array 2011-04-29 21459883 Villard E 2011-04-01 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/21459883 A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. Idiopathic dilated cardiomyopathy 1,179 European ancestry cases, 1,108 European ancestry controls 1,165 European ancestry cases, 1,302 European ancestry controls Illumina [517382] 2 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST001023 Genome-wide genotyping array 2013-04-17 23341777 Dong J 2013-01-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23341777 Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese. Squamous cell carcinoma 833 Han Chinese ancestry cases, 3,094 Han Chinese ancestry controls 2,223 Han Chinese ancestry cases, 6,409 Han Chinese ancestry controls Affymetrix [570009] 1 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST001827 Genome-wide genotyping array 2010-06-09 20460270 Garcia-Barcelo MM 2010-05-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20460270 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. Biliary atresia 281 Chinese ancestry cases, 481 Chinese ancestry controls 124 Chinese ancestry cases, 90 Chinese ancestry controls Affymetrix [289118] 3 biliary atresia http://purl.obolibrary.org/obo/MONDO_0008867 GCST000681 Genome-wide genotyping array 2010-04-12 20304771 Newman AB 2010-03-18 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/20304771 A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. Longevity 1,836 European ancestry long-lived individuals, 1,955 European ancestry controls 2,594 European ancestry long-lived individuals, 3,431 European ancestry controls Affymetrix, Illumina [2287520] (imputed) 1 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST000632 Genome-wide genotyping array 2009-05-07 19401414 Takeuchi F 2009-04-29 Diabetes www.ncbi.nlm.nih.gov/pubmed/19401414 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. Type 2 diabetes 519 Japanese ancestry cases, 503 Japanese ancestry controls 5,110 Japanese ancestry cases, 6,867 Japanese ancestry controls Illumina [482625] 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000383 Genome-wide genotyping array 2008-09-15 17903295 Lunetta KL 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903295 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Aging traits 1,345 individuals from 330 families NA Affymetrix [70897] 10 obsolete aging, age at menopause, exercise test, age at death http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004704, http://www.ebi.ac.uk/efo/EFO_0004328, http://www.ebi.ac.uk/efo/EFO_0005056 GCST000096 Genome-wide genotyping array 2008-09-10 17903295 Lunetta KL 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903295 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. Morbidity-free survival 558 individuals NA Affymetrix [70897] 5 disease free survival http://www.ebi.ac.uk/efo/EFO_0000409 GCST000103 Genome-wide genotyping array 2013-12-03 23725790 Renteria ME 2013-06-03 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/23725790 GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. DNA methylation (parent-of-origin) 1,024 European ancestry individuals NA Illumina [515966] 7 DNA methylation http://purl.obolibrary.org/obo/GO_0006306 GCST002057 Genome-wide genotyping array 2013-12-03 23725790 Renteria ME 2013-06-03 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/23725790 GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association. DNA methylation (variation) 256 European ancestry individuals 384 European ancestry individuals Illumina [515966] 19 DNA methylation http://purl.obolibrary.org/obo/GO_0006306 GCST002058 Genome-wide genotyping array 2013-03-20 23263863 Li J 2012-12-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23263863 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Mean corpuscular hemoglobin 7,943 African American children, 6,234 European ancestry children NA Illumina [544917] 10 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST001780 Genome-wide genotyping array 2013-03-15 23263863 Li J 2012-12-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23263863 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Hematology traits 7,943 African American children, 6,234 European ancestry children NA Illumina [544917] 12 hemoglobin measurement, leukocyte count, erythrocyte count, hematocrit http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004308, http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004348 GCST001779 Genome-wide genotyping array 2013-03-15 23263863 Li J 2012-12-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23263863 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Mean corpuscular hemoglobin concentration 7,943 African American children, 6,234 European ancestry children NA Illumina [544917] 6 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST001782 Genome-wide genotyping array 2013-03-15 23263863 Li J 2012-12-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23263863 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Mean corpuscular volume 7,943 African American children, 6,234 European ancestry children NA Illumina [544917] 10 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST001781 Genome-wide genotyping array 2013-03-15 23263863 Li J 2012-12-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23263863 GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Platelet count 7,943 African American children, 6,234 European ancestry children NA Illumina [544917] 8 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST001783 Genome-wide genotyping array 2014-03-27 24068962 O'Seaghdha CM 2013-09-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24068962 Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. Calcium levels 39,400 European ancestry individuals Up to 21,679 European ancestry individuals Affymetrix, Illumina [2500000] (imputed) 13 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST002201 Genome-wide genotyping array 2013-09-14 23612905 Zhao SX 2013-04-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23612905 Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. Graves' disease 1,442 Han Chinese ancestry cases, 1,468 Han Chinese ancestry controls 7,891 Han Chinese ancestry cases, 8,351 Han Chinese ancestry controls Illumina [8019905] (imputed) 5 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST001984 Genome-wide genotyping array 2013-09-14 23612905 Zhao SX 2013-04-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23612905 Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis. Graves' disease 1,442 Han Chinese ancestry cases, 1,468 Han Chinese ancestry controls 6,358 Han Chinese ancestry cases, 6,722 Han Chinese ancestry controls Illumina [483947] 1 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST001982 Genome-wide genotyping array 2013-03-19 23279374 Athanasiadis G 2013-01-02 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/23279374 Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain. β2-Glycoprotein I (β2-GPI) plasma levels 306 European ancestry individuals NA Illumina [283437] 9 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST001800 Genome-wide genotyping array 2013-06-28 23467860 Pare G 2013-03-06 Circulation www.ncbi.nlm.nih.gov/pubmed/23467860 Genetic determinants of dabigatran plasma levels and their relation to bleeding. Response to dabigatran etexilate treatment 1,490 European ancestry atrial fibrillation cases at risk of stroke 204 European ancestry atrial fibrillation cases at risk of stroke, 66 Latin American atrial fibrillation cases at risk of stroke, 1 Arab ancestry atrial fibrillation cases at risk of stroke, 5 Black African atrial fibrillation cases at risk of stroke, 25 East Asian ancestry atrial fibrillation cases at risk of stroke, 1 Colored African atrial fibrillation cases at risk of stroke, 9 South Asian ancestry atrial fibrillation cases at risk of stroke, 15 Asian ancestry atrial fibrillation cases at risk of stroke, 134 atrial fibrillation cases at risk of stroke Illumina [551203] 2 response to dabigatran etexilate http://www.ebi.ac.uk/efo/EFO_0005205 GCST001895 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Red blood cell count 14,392 Japanese ancestry individuals NA Illumina [561583] 8 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST000588 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. White blood cell count 14,677 Japanese ancestry individuals NA Illumina [561583] 5 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST000589 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Mean corpuscular hemoglobin concentration 14,377 Japanese ancestry individuals NA Illumina [561583] 7 hemoglobin measurement, mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004528 GCST000582 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Triglycerides 8,993 Japanese ancestry individuals NA Illumina [561583] 6 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000584 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Platelet count 14,806 Japanese ancestry individuals NA Illumina [561583] 7 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST000580 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Mean corpuscular hemoglobin Up to 14,362 Japanese ancestry individuals NA Illumina [561583] 15 hemoglobin measurement, mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004527 GCST000587 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Urate levels 8,868 Japanese ancestry individuals NA Illumina [561583] 5 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST000581 Genome-wide genotyping array 2013-11-05 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Hematological and biochemical traits Up to 14,402 Japanese individuals NA Illumina [561583] 29 serum albumin measurement, aspartate aminotransferase measurement, alkaline phosphatase measurement, hemoglobin measurement, creatinine measurement, serum alanine aminotransferase measurement, serum gamma-glutamyl transferase measurement, hematocrit, creatine kinase measurement, protein measurement, uric acid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004535, http://www.ebi.ac.uk/efo/EFO_0004736, http://www.ebi.ac.uk/efo/EFO_0004533, http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0004532, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0004534, http://www.ebi.ac.uk/efo/EFO_0004747, http://www.ebi.ac.uk/efo/EFO_0004761, http://www.ebi.ac.uk/efo/EFO_0004612 GCST000583 Genome-wide genotyping array 2013-09-04 20139978 Kamatani Y 2010-02-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20139978 Genome-wide association study of hematological and biochemical traits in a Japanese population. Mean corpuscular volume 14,364 Japanese ancestry individuals NA Illumina [561583] 17 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST000585 Genome-wide genotyping array 2012-08-15 22703881 Tang W 2012-06-14 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22703881 Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. Activated partial thromboplastin time 9,240 European ancestry individuals 2611 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 9 partial thromboplastin time http://www.ebi.ac.uk/efo/EFO_0004310 GCST001574 Genome-wide genotyping array 2012-08-15 22703881 Tang W 2012-06-14 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22703881 Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease. Prothrombin time 2,583 European ancestry individuals 986 European ancestry individuals Illumina [~ 2500000] (imputed) 2 prothrombin time measurement http://www.ebi.ac.uk/efo/EFO_0008390 GCST001573 Genome-wide genotyping array 2012-07-17 22658931 Pajewski NM 2012-05-30 Vaccine www.ncbi.nlm.nih.gov/pubmed/22658931 A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed. Immune response to anthrax vaccine 726 European ancestry individuals NA Affymetrix [736996] 8 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST001547 Genome-wide genotyping array 2014-04-02 24068947 Brandler WM 2013-09-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24068947 Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. Relative hand skill in reading disability 728 European ancestry individuals with reading disability NA Illumina [2095209] 10 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST002183 Genome-wide genotyping array 2014-04-02 24068947 Brandler WM 2013-09-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24068947 Common variants in left/right asymmetry genes and pathways are associated with relative hand skill. Relative hand skill 2,666 European ancestry individuals NA Illumina [NR] 3 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST002185 Genome-wide genotyping array 2013-03-22 23303382 Hong KW 2013-01-10 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23303382 Genome-wide association study of serum albumin:globulin ratio in Korean populations. Hematology traits 4,637 East Asian ancestry individuals 4,205 East Asian ancestry individuals Affymetrix [290659] 5 albumin:globulin ratio measurement http://www.ebi.ac.uk/efo/EFO_0005128 GCST001813 Genome-wide genotyping array 2011-07-13 21700879 Qi L 2011-06-23 Diabetes www.ncbi.nlm.nih.gov/pubmed/21700879 Novel locus FER is associated with serum HMW adiponectin levels. Adiponectin levels 1,591 European ancestry female individuals 626 European ancestry individuals from 235 families Affymetrix [2543887] (imputed) 5 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST001122 Genome-wide genotyping array 2012-06-20 22538805 Tantisira KG 2012-04-26 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/22538805 Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus. Asthma 418 European ancestry cases 407 European ancestry cases Affymetrix [444088] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001495 Genome-wide genotyping array 2012-11-02 20889312 Wang KS 2010-10-01 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/20889312 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. Bipolar disorder and schizophrenia 651 European ancestry bipolar cases, 1,171 European ancestry schizophrenia cases, 2,412 European ancestry controls NA Affymetrix [722112] 103 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST000821 Genome-wide genotyping array 2012-03-09 22293688 Huang J 2012-02-01 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22293688 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Type 1 diabetes 16,179 European ancestry individuals NA NR [6233112] (imputed) 2 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST001394 Genome-wide genotyping array 2012-03-10 22293688 Huang J 2012-02-01 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22293688 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Type 2 diabetes 16,179 European ancestry individuals NA NR [6233112] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001397 Genome-wide genotyping array 2012-03-10 22293688 Huang J 2012-02-01 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22293688 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. Crohn's disease 16,179 European ancestry individuals NA NR [6233112] (imputed) 1 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST001396 Genome-wide genotyping array 2010-12-01 20953188 Ellinghaus E 2010-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20953188 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. Psoriasis 472 European ancestry cases, 1,146 European ancestry controls 2,668, European ancestry cases, 762 French Canadian founder population cases, 2,585 cases, 3,485 European ancestry controls, 994 French Canadian founder population controls, 2,412 controls Illumina [2339118] (imputed) 3 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST000836 Genome-wide genotyping array 2010-09-28 20800221 Terracciano A 2010-08-25 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20800221 Genome-wide association scan of trait depression. Depression (quantitative trait) 3,972 Sardinian individuals, 839 European ancestry individuals NA Affymetrix, Illumina [up to 2500000] (imputed) 11 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST000779 Genome-wide genotyping array 2009-12-18 19944697 Karlsen TH 2009-11-25 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/19944697 Genome-wide association analysis in primary sclerosing cholangitis. Primary sclerosing cholangitis 285 European ancestry cases, 298 European ancestry controls 766 European ancestry cases, 2,935 European ancestry controls Affymetrix [375487] 0 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST000534 Genome-wide genotyping array 2010-01-19 20044523 Debette S 2009-12-31 Stroke www.ncbi.nlm.nih.gov/pubmed/20044523 Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium. Subclinical brain infarct 9,401 European ancestry individuals 1,822 European ancestry individuals, 644 Black individuals Affymetrix, Illumina [2217889] (imputed) 0 MRI defined brain infarct http://www.ebi.ac.uk/efo/EFO_0004715 GCST000554 Genome-wide genotyping array 2012-07-03 22554406 Kang SJ 2012-05-03 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/22554406 Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6. Electroencephalographic traits in alcoholism 1,560 European ancestry individuals from 117 families NA Illumina [634583] 8 frontal theta oscillation measurement http://www.ebi.ac.uk/efo/EFO_0004800 GCST001503 Genome-wide genotyping array 2011-11-26 22027810 Forstbauer LM 2011-10-26 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22027810 Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata. Alopecia areata 729 European ancestry cases, 656 European ancestry controls 991 European ancestry cases, 2,021 European ancestry controls Illumina [487932] 0 alopecia areata http://www.ebi.ac.uk/efo/EFO_0004192 GCST001295 Genome-wide genotyping array 2012-07-31 22678113 Cox HC 2012-06-08 Neurogenetics www.ncbi.nlm.nih.gov/pubmed/22678113 A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility. Migraine 76 Norfolk Island (founder or genetic isolate) cases, 209 Norfolk Island (founder or genetic isolate) controls 4,705 European ancestry cases, 21,008 European ancestry controls Illumina [544590] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST001562 Genome-wide genotyping array 2015-04-14 21699788 Okada Y 2011-06-20 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/21699788 HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease. Ulcerative colitis or Crohn's disease 372 Japanese ancestry Crohn's disease cases, 372 Japanese ancestry ulcerative colitis cases 607 Japanese ancestry Crohn's disease cases, 376 Japanese ancestry ulcerative colitis cases Illumina [461368] 2 ulcerative colitis, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0000384 GCST001118 Genome-wide genotyping array 2013-06-20 23496005 Luca G 2013-03-18 J Sleep Res www.ncbi.nlm.nih.gov/pubmed/23496005 Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study. Narcolepsy with cataplexy 585 European ancestry cases 387 European ancestry cases NR [NR] 4 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST001909 Genome-wide genotyping array 2011-07-13 21700618 Nan H 2011-06-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21700618 Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma. Basal cell carcinoma 2,045 European ancestry cases, 6,013 European ancestry controls 1,426 cases, 4,845 controls Affymetrix, Illumina [2318094] (imputed) 3 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST001124 Genome-wide genotyping array 2015-05-12 21696813 Schauberger EM 2011-06-20 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/21696813 Identification of ATPAF1 as a novel candidate gene for asthma in children. Asthma (childhood onset) 112 European ancestry child cases, 165 European ancestry child controls 1,481 European ancestry individuals from 341 families, 429 European ancestry trios, 52 African American trios, 1,231 Hispanic trios, 46 trios, 6,475 European ancestry controls Affymetrix [98921] 0 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST001117 Genome-wide genotyping array 2009-04-13 19340012 Nan H 2009-04-02 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/19340012 Genome-wide association study of tanning phenotype in a population of European ancestry. Tanning 2,287 European ancestry female individuals 870 European ancestry female individuals Illumina [528173] 10 suntan http://www.ebi.ac.uk/efo/EFO_0004279 GCST000371 Genome-wide genotyping array 2011-10-11 21909109 Kim YJ 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909109 Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. Gamma glutamyl transpeptidase 12,545 Korean ancestry individuals Up to 30,395 East Asian ancestry individuals Affymetrix [~ 2200000] (imputed) 7 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST001234 Genome-wide genotyping array 2011-10-11 21909109 Kim YJ 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909109 Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. HDL cholesterol 12,545 Korean ancestry individuals Up to 30,395 East Asian ancestry individuals Affymetrix [~ 2200000] (imputed) 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST001237 Genome-wide genotyping array 2011-10-11 21909109 Kim YJ 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909109 Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. Metabolite levels 12,545 Korean ancestry individuals Up to 30,395 East Asian ancestry individuals Affymetrix [~ 2200000] (imputed) 18 serum albumin measurement, metabolite measurement, serum alanine aminotransferase measurement, low density lipoprotein cholesterol measurement, fasting blood glucose measurement, uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004535, http://www.ebi.ac.uk/efo/EFO_0004725, http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004465, http://www.ebi.ac.uk/efo/EFO_0004761 GCST001233 Genome-wide genotyping array 2011-10-11 21909109 Kim YJ 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909109 Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. Triglycerides 12,545 Korean ancestry individuals Up to 30,395 East Asian ancestry individuals Affymetrix [~ 2200000] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST001230 Genome-wide genotyping array 2008-06-16 17653210 Maeda S 2007-08-01 Kidney Int Suppl www.ncbi.nlm.nih.gov/pubmed/17653210 Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population. Type 2 diabetes nephropathy 94 Japanese ancestry cases, 94 Japanese ancestry controls NA NR [~ 80000] 1 diabetic nephropathy, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000401, http://purl.obolibrary.org/obo/MONDO_0005148 GCST000064 Genome-wide genotyping array 2011-01-14 20801717 Shatunov A 2010-10-01 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/20801717 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. Amyotrophic lateral sclerosis 4,857 European ancestry cases, 8,987 European ancestry controls NA Illumina [227475] 4 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000820 Genome-wide genotyping array 2011-05-26 21502949 Stein JL 2011-04-19 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21502949 Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. Caudate nucleus volume 734 European ancestry individuals 464 European ancestry individuals Illumina [520459] 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST001045 Genome-wide genotyping array 2012-02-11 22279548 Sebastiani P 2012-01-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/22279548 Genetic signatures of exceptional longevity in humans. Longevity 801 European ancestry long-living individuals, 914 European ancestry controls 292 European ancestry long-living individuals, 21 long-living individuals, 867 controls Illumina [243980] 0 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST001379 Genome-wide genotyping array 2011-01-06 21088011 Erdmann J 2010-11-18 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/21088011 Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. Coronary heart disease 1,157 European ancestry cases, 1,748 European ancestry controls 7,887 European ancestry cases, 8,244 European ancestry controls Affymetrix [254558] 1 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000875 Genome-wide genotyping array 2011-01-08 21107309 McClay JL 2010-11-24 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/21107309 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. Response to antipsychotic treatment in schizophrenia (working memory) 738 European ancestry, African American, and other ancestry cases NA Affymetrix [492900] 11 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST000883 Genome-wide genotyping array 2011-01-08 21107309 McClay JL 2010-11-24 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/21107309 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. Response to antipsychotic treatment 738 European ancestry, African American, and other ancestry cases NA Affymetrix [492900] 2 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST000884 Genome-wide genotyping array 2011-01-08 21107309 McClay JL 2010-11-24 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/21107309 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. Response to antipsychotic treatment in schizophrenia (reasoning) 738 European ancestry, African American, and other ancestry cases NA Affymetrix [492900] 10 reasoning http://www.ebi.ac.uk/efo/EFO_0004350 GCST000885 Genome-wide genotyping array 2011-11-30 22028671 Surakka I 2011-10-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22028671 A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. Lipid traits Up to 32,225 European ancestry individuals 11,509 European ancestry individuals, 11,163 individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST001289 Genome-wide genotyping array 2011-11-16 21991891 Tantisira KG 2011-09-26 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/21991891 Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma. Asthma treatment response 1,169 European ancestry child and parent asthmatic cases 935 European ancestry adult asthmatic cases Illumina [534290] 0 response to glucocorticoid http://purl.obolibrary.org/obo/GO_0051384 GCST001252 Genome-wide genotyping array 2013-09-07 23642732 Cox AJ 2013-04-19 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/23642732 Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study. Bilirubin levels 1,180 European ancestry individuals from ~475 families Affymetrix, Illumina [371951] 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST001976 Genome-wide genotyping array 2009-09-04 19684604 Papaemmanuil E 2009-08-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19684604 Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. Acute lymphoblastic leukemia (childhood) 907 European ancestry cases, 2,398 European ancestry controls NA Illumina [291473] 3 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST000463 Genome-wide genotyping array 2013-07-25 23539754 Yamada Y 2013-03-28 J Med Genet www.ncbi.nlm.nih.gov/pubmed/23539754 Identification of chromosome 3q28 and ALPK1 as susceptibility loci for chronic kidney disease in Japanese individuals by a genome-wide association study. Chronic kidney disease 252 Japanese ancestry cases, 249 Japanese ancestry controls 1,100 Japanese ancestry cases, 2,250 Japanese ancestry controls Illumina [297707] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST001924 Genome-wide genotyping array 2011-12-02 22037551 Shi Y 2011-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22037551 A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1. Gastric cancer 1,006 Han Chinese ancestry cases, 2,273 Han Chinese ancestry controls 3,288 Han Chinese ancestry cases, 3,609 Han Chinese ancestry controls Affymetrix [555896] 2 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST001300 Genome-wide genotyping array 2011-12-14 22087292 Sun L 2011-11-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/22087292 Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass. Femoral neck bone geometry 1,627 Han Chinese ancestry individuals 2,286 European ancestry individuals Affymetrix [689368] 2 femoral neck bone geometry http://www.ebi.ac.uk/efo/EFO_0004511 GCST001315 Genome-wide genotyping array 2013-05-09 23376709 Kerns SL 2013-01-31 J Urol www.ncbi.nlm.nih.gov/pubmed/23376709 A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of urinary symptoms after radiotherapy for prostate cancer. Urinary symptoms in response to radiotherapy in prostate cancer 346 European, African, Hispanic and Asian ancestry individuals 377 European, African, Hispanic and Asian ancestry individuals Affymetrix [613496] 1 response to radiation, lower urinary tract symptom http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0008008 GCST001847 Genome-wide genotyping array 2013-09-12 23563607 Berndt SI 2013-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23563607 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Obesity 93,015 European ancestry overweight individuals, 32,858 European ancestry class I obese individuals, 9,889 European ancestry class II obese individuals, 2,896 European ancestry class III obese individuals, up to 65,840 European ancestry controls 65,332 European ancestry overweight individuals, 22,373 European ancestry class I obese individuals, 5,476 European ancestry class II obese individuals, 1,162 European ancestry class III obese individuals, up to 39,294 European ancestry controls Affymetrix, Illumina [~ 2800000] (imputed) 66 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST001953 Genome-wide genotyping array 2013-09-12 23563607 Berndt SI 2013-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23563607 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Waist-hip ratio 4,774 European ancestry high waist-to-hip ratio individuals, 5,481 European ancestry low waist-to-hip ratio individuals 3,351 European ancestry high waist-to-hip ratio individuals, 3,352 European ancestry low waist-to-hip ratio individuals Affymetrix, Illumina [~ 2800000] (imputed) 4 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST001954 Genome-wide genotyping array 2013-09-12 23563607 Berndt SI 2013-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23563607 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Body mass index 7,962 European ancestry high body mass index individuals, 8,106 European ancestry low body mass index individuals 4,900 European ancestry high body mass index individuals, 4,891 European ancestry low body mass index individuals Affymetrix, Illumina [~ 2800000] (imputed) 10 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001955 Genome-wide genotyping array 2013-09-12 23563607 Berndt SI 2013-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23563607 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Height 8,097 European ancestry tall individuals, 8,099 European ancestry short individuals 4,872 European ancestry tall individuals, 4,831 European ancestry short individuals Affymetrix, Illumina [~ 2800000] (imputed) 86 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST001956 Genome-wide genotyping array 2013-08-23 23583978 Monda KL 2013-04-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23583978 A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Body mass index 37,956 African American individuals, 1,188 Nigerian ancestry individuals 27,661 African America/Afro-Caribbean individuals, 4,607 Sub-Saharan African ancestry individuals, 123,706 European ancestry inidividuals Affymetrix, Illumina [3283202] (imputed) 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001967 Genome-wide genotyping array 2015-06-27 25187353 Goldstein JI 2014-09-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25187353 Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles. Clozapine-induced agranulocytosis 161 European ancestry cases, 1,196 European ancestry clozapine-treated and untreated controls NA Illumina [8809853] (imputed) 28 Drug-induced agranulocytosis, response to clozapine http://purl.obolibrary.org/obo/HP_0012235, http://purl.obolibrary.org/obo/GO_0097338 GCST002595 Genome-wide genotyping array 2011-05-11 21499248 Kumar V 2011-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21499248 Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma. Hepatocellular carcinoma 721 Japanese ancestry cases, 2,890 Japanese ancestry controls 673 Japanese ancestry cases, 2,596 Japanese ancestry controls Illumina [432703] 2 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST001041 Genome-wide genotyping array 2012-01-04 22105264 Allen-Brady K 2011-12-01 Obstet Gynecol www.ncbi.nlm.nih.gov/pubmed/22105264 Identification of six loci associated with pelvic organ prolapse using genome-wide association analysis. Pelvic organ prolapse 115 European ancestry cases, 2,976 European ancestry controls 76 European ancestry cases Illumina [499948] 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST001340 Genome-wide genotyping array 2014-02-25 24144296 Cheng CY 2013-08-08 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24144296 Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Axial length 12,531 European ancestry individuals 8,216 Asian ancestry individuals Illumina [2500000] (imputed) 21 axial length measurement http://www.ebi.ac.uk/efo/EFO_0005318 GCST002115 Genome-wide genotyping array 2013-04-11 23300138 He M 2013-01-07 Gut www.ncbi.nlm.nih.gov/pubmed/23300138 A genome wide association study of genetic loci that influence tumour biomarkers cancer antigen 19-9, carcinoembryonic antigen and α fetoprotein and their associations with cancer risk. Tumor biomarkers 3,451 Han Chinese ancestry individuals 10,326 Chinese ancestry individuals Affymetrix, Illumina [NR] (imputed) 11 cancer biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005127 GCST001808 Genome-wide genotyping array 2009-05-28 19448620 Perry JR 2009-05-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19448620 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. Menarche (age at onset) 17,510 European ancestry female individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 2 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST000404 Genome-wide genotyping array 2013-04-09 22982463 Tang WH 2012-09-13 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/22982463 Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk. Paraoxonase activity 2,136 European ancestry individuals NA Affymetrix [2421770] (imputed) 2 arylesterase enzyme measurement http://www.ebi.ac.uk/efo/EFO_0005126 GCST001677 Genome-wide genotyping array 2011-12-03 22044751 Foster MC 2011-11-01 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/22044751 Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study. Renal sinus fat 2,809 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 8 renal sinus adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004864 GCST001304 Genome-wide genotyping array 2011-11-30 22029572 Simonson MA 2011-10-26 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/22029572 Recent methods for polygenic analysis of genome-wide data implicate an important effect of common variants on cardiovascular disease risk. Cardiovascular disease risk factors 1,772 individuals NA Affymetrix [258891] 0 cardiovascular measurement http://www.ebi.ac.uk/efo/EFO_0004298 GCST001294 Genome-wide genotyping array 2011-12-23 22105620 Papassotiropoulos A 2011-11-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22105620 A genome-wide survey and functional brain imaging study identify CTNNBL1 as a memory-related gene. Memory performance 1,073 European ancestry individuals 524 individuals Affymetrix [582514] 0 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST001327 Genome-wide genotyping array 2015-05-11 23517042 Melen E 2013-04-01 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/23517042 Genome-wide association study of body mass index in 23 000 individuals with and without asthma. Body mass index in non-asthmatics 6,025 European ancestry children, 567 children, 6,334 European ancestry adult individuals, 2,050 adult individuals NA Illumina [up to 527642] 9 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001935 Genome-wide genotyping array 2015-05-11 23517042 Melen E 2013-04-01 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/23517042 Genome-wide association study of body mass index in 23 000 individuals with and without asthma. Body mass index in asthmatics 1,881 European ancestry children, 810 children, 2,643 European ancestry adult individuals, 817 adult individuals 979 European ancestry children, 921 Hispanic children, 120 children Illumina [up to 536451] 6 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001945 Genome-wide genotyping array 2012-08-14 22832961 Kamboh MI 2012-05-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/22832961 Genome-wide association study of Alzheimer's disease. Alzheimer's disease 1,291 European ancestry cases, 938 European ancestry controls 509 European ancestry cases, 753 European ancestry controls, 2,218 cases, 2,583 controls Illumina [2543888] (imputed) 8 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001529 Genome-wide genotyping array 2010-10-07 20871597 Miki D 2010-09-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20871597 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. Lung adenocarcinoma 1,004 Japanese ancestry cases, 1,900 Japanese ancestry controls 1,094 East Asian ancestry cases, 9,148 East Asian ancestry controls Illumina [432024] 2 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST000810 Genome-wide genotyping array 2012-12-04 23017229 Voruganti VS 2012-09-24 Cytokine www.ncbi.nlm.nih.gov/pubmed/23017229 Genome-wide association replicates the association of Duffy antigen receptor for chemokines (DARC) polymorphisms with serum monocyte chemoattractant protein-1 (MCP-1) levels in Hispanic children. Monocyte chemoattractant protein-1 levels 815 Hispanic children NA Illumina [NR] 5 CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004749 GCST001691 Genome-wide genotyping array 2014-04-25 24143882 Gelernter J 2013-10-19 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24143882 Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways. Opioid sensitivity 1,383 European ancestry cases, 996 European ancestry controls, 683 African American cases, 2,635 African American controls 2,116 European ancestry individuals, 4,496 African American individuals Illumina [988306] 3 response to isoquinoline alkaloid http://purl.obolibrary.org/obo/GO_0014072 GCST002235 Genome-wide genotyping array 2013-01-29 23149075 Aslibekyan S 2012-11-10 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/23149075 Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network. Response to fenofibrate (adiponectin levels) 793 European ancestry individuals NA Affymetrix [2543887] (imputed) 12 response to fenofibrate http://purl.obolibrary.org/obo/GO_1901557 GCST001738 Genome-wide genotyping array 2012-08-07 22700719 Slager SL 2012-06-13 Blood www.ncbi.nlm.nih.gov/pubmed/22700719 Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia. Chronic lymphocytic leukemia 1,121 European ancestry cases, 3,745 European ancestry controls 861 European ancestry cases, 2,033 European ancestry controls Affymetrix, Illumina [~ 1500000] (imputed) 8 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST001570 Genome-wide genotyping array 2013-05-01 23364394 Lee JY 2013-01-31 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23364394 A genome-wide association study of a coronary artery disease risk variant. Coronary heart disease 2,123 Korean ancestry cases, 3,591 Korean ancestry controls 3,052 Japanese ancestry cases, 4,976 Japanese ancestry controls Affymetrix [521786] 5 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001845 Genome-wide genotyping array 2013-06-27 23541324 Li X 2013-03-27 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/23541324 Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients. Pulmonary function in asthmatics 1,544 European ancestry individuals Illumina [369771] 4 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST001918 Genome-wide genotyping array 2013-04-24 21497773 Ziliak D 2011-02-08 Transl Res www.ncbi.nlm.nih.gov/pubmed/21497773 Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers. Response to platinum-based chemotherapy in head and neck cancers 90 East Asian ancestry lymphoblastoid cell lines 90 European ancestry lymphoblastoid cell lines, 59 Yoruban ancestry lymphoblastoid cell lines NR [~ 2000000] 0 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST000968 Genome-wide genotyping array 2013-04-25 21497773 Ziliak D 2011-02-08 Transl Res www.ncbi.nlm.nih.gov/pubmed/21497773 Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers. Response to platinum-based chemotherapy in head and neck cancers 90 European ancestry Lymphoblastoid cell lines NA NR [~ 2000000] 0 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST000967 Genome-wide genotyping array 2013-01-30 23149450 Otowa T 2012-11-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/23149450 Meta-analysis of genome-wide association studies for panic disorder in the Japanese population. Panic disorder 718 Japanese ancestry cases, 1,717 Japanese ancestry controls 329 Japanese ancestry cases, 861 Japanese ancestry controls Affymetrix [1900000] (imputed) 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST001742 Genome-wide genotyping array 2009-06-04 19461586 Norris JM 2009-05-21 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/19461586 Genome-wide association study and follow-up analysis of adiposity traits in Hispanic Americans: the IRAS Family Study. Obesity-related traits 229 Hispanic individuals from 34 families 961 Hispanic individuals from 59 families Illumina [309200] 0 adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004764 GCST000409 Genome-wide genotyping array 2012-11-20 22959728 Ahmeti KB 2012-09-05 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22959728 Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Amyotrophic lateral sclerosis (age of onset) 4,243 European ancestry cases NA Illumina [254145] 13 age of onset of amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/OBA_2001018 GCST001663 Genome-wide genotyping array 2012-11-20 22959728 Ahmeti KB 2012-09-05 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22959728 Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Amyotrophic lateral sclerosis 4,243 European ancestry cases, 5,112 European ancestry controls NA Illumina [254145] 15 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST001664 Genome-wide genotyping array 2017-09-28 22959728 Ahmeti KB 2012-09-05 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22959728 Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Amyotrophic lateral sclerosis (C9orf72 mutation interaction) 4,243 European ancestry cases NA Illumina [254145] 3 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST004791 Genome-wide genotyping array 2017-09-28 22959728 Ahmeti KB 2012-09-05 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22959728 Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Amyotrophic lateral sclerosis in C9orf72 mutation negative individuals Up to 4,243 European ancestry cases, up to 5,112 European ancestry controls NA Illumina [254145] 4 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST004793 Genome-wide genotyping array 2017-09-28 22959728 Ahmeti KB 2012-09-05 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22959728 Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1. Amyotrophic lateral sclerosis in C9orf72 mutation positive individuals up to 4,243 European ancestry cases, up to 5,112 European ancestry controls NA Illumina [254145] 6 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST004792 Genome-wide genotyping array 2012-10-09 22886559 Rajaraman P 2012-08-11 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22886559 Genome-wide association study of glioma and meta-analysis. Glioma 1,856 European ancestry cases, 4,955 European ancestry controls 5,015 European ancestry cases, 11,601 European ancestry controls Illumina [559977] 3 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST001633 Genome-wide genotyping array 2011-05-26 21493818 Shaw SY 2011-04-21 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/21493818 Genetic and clinical correlates of early-outgrowth colony-forming units. Monocyte early outgrowth colony forming units 1,654 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 3 monocyte early outgrowth colony forming unit http://www.ebi.ac.uk/efo/EFO_0004506 GCST001048 Genome-wide genotyping array 2009-09-28 19729412 Tonjes A 2009-09-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19729412 Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs. Height 929 Sorbian (founder/genetic isolate) individuals 5,758 European ancestry individuals Affymetrix [390619] 1 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000475 Genome-wide genotyping array 2012-12-06 22993228 Williams FM 2012-09-19 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/22993228 Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects. Disc degeneration (lumbar) 4,683 European ancestry individuals NA Affymetrix, Illumina [2552511] (imputed) 35 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST001687 Genome-wide genotyping array 2012-11-28 22885689 Levinson DF 2012-09-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/22885689 Genome-wide association study of multiplex schizophrenia pedigrees. Schizophrenia 1,218 European ancestry cases, 990 European ancestry controls, 139 cases, 114 controls NA Illumina [up to 531195] 11 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001657 Genome-wide genotyping array 2014-05-13 24185611 Cook MB 2013-11-02 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24185611 A genome-wide association study of prostate cancer in West African men. Prostate cancer 474 West African ancestry cases, 458 West African ancestry controls 5,096 African American cases, 4,972 African American controls Illumina [2837019] 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002264 Genome-wide genotyping array 2013-01-09 23100282 Hopewell JC 2012-10-24 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/23100282 Impact of common genetic variation on response to simvastatin therapy among 18 705 participants in the Heart Protection Study. Response to statin therapy 3,895 European ancestry individuals 14,810 individuals Illumina [546210] 0 response to statin http://purl.obolibrary.org/obo/GO_0036273 GCST001716 Genome-wide genotyping array 2011-10-29 21996601 Das K 2011-10-11 Hum Hered www.ncbi.nlm.nih.gov/pubmed/21996601 Genome-wide association studies for bivariate sparse longitudinal data. Blood pressure 500 European ancestry male individuals, 477 European ancestry female individuals NA NR [~ 550000] 0 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST001270 Genome-wide genotyping array 2012-11-30 22982992 Yang J 2012-09-12 Nature www.ncbi.nlm.nih.gov/pubmed/22982992 FTO genotype is associated with phenotypic variability of body mass index. Body mass index 133,154 European ancestry individuals 59,325 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2440000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001676 Genome-wide genotyping array 2015-05-06 22889921 Stewart SE 2012-08-14 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22889921 Genome-wide association study of obsessive-compulsive disorder. Obsessive-compulsive disorder 1,279 European ancestry cases, 5,139 European ancestry controls, 299 European ancestry trios, 93 South African Afrikaner ancestry cases, 158 South African Afrikaner ancestry controls, 93 Ashkenazi Jewish cases, 260 Ashkenazi Jewish controls, 101 Hispanic and unknown ancestry trios NA Illumina [479067] 3 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST001636 Genome-wide genotyping array 2011-07-12 21698141 Freedman BI 2011-06-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21698141 Differential effects of MYH9 and APOL1 risk variants on FRMD3 Association with Diabetic ESRD in African Americans. End-stage renal disease 952 African American cases, 988 African American controls 640 African American cases, 683 African American controls Affymetrix [832357] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST001107 Genome-wide genotyping array 2010-10-15 20876614 Yoon KA 2010-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20876614 A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population. Non-small cell lung cancer 621 Korean ancestry cases, 1,541 Korean ancestry controls 804 Korean ancestry cases, 1,470 Korean ancestry controls Affymetrix [246758] 3 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST000815 Genome-wide genotyping array 2012-11-30 23028347 Liu F 2012-09-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23028347 A genome-wide association study identifies five loci influencing facial morphology in Europeans. Facial morphology 5,388 European ancestry individuals 4,071 European ancestry individuals Affymetrix, Illumina [2558979] (imputed) 0 facial morphology http://www.ebi.ac.uk/efo/EFO_0004743 GCST001678 Genome-wide genotyping array 2012-09-18 22814818 Hoehn R 2012-07-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22814818 Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness. Central corneal thickness 3,931 European ancestry individuals 1,418 European ancestry individuals Affymetrix [NR] (imputed) 2 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST001614 Genome-wide genotyping array 2011-07-21 20834067 Yashin AI 2010-09-01 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/20834067 Joint influence of small-effect genetic variants on human longevity. Longevity 1,173 individuals NA NR [~ 550000] 39 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST000785 Genome-wide genotyping array 2012-12-02 23001122 Orr N 2012-09-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23001122 Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk. Breast cancer (male) 823 European ancestry cases, 2,795 European ancestry controls 438 European ancestry cases, 474 European ancestry controls Illumina [447760] 3 male breast carcinoma http://www.ebi.ac.uk/efo/EFO_0006861 GCST001690 Genome-wide genotyping array 2012-10-24 21833088 Sawcer S 2011-08-11 Nature www.ncbi.nlm.nih.gov/pubmed/21833088 Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Multiple sclerosis 9,772 European ancestry cases, 16,849 European ancestry controls 4,218 European ancestry cases, 7,296 European ancestry controls Illumina [465434] 87 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST001198 Genome-wide genotyping array 2012-04-28 22456796 Imamura M 2012-03-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22456796 A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations. Type 2 diabetes 4,470 Japanese ancestry cases, 3,071 Japanese ancestry controls 7,605 Japanese ancestry cases, 3,534 Japanese ancestry controls NR [2229890] (imputed) 4 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001461 Genome-wide genotyping array 2012-05-25 22504419 Taal HR 2012-04-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22504419 Common variants at 12q15 and 12q24 are associated with infant head circumference. Head circumference (infant) 10,768 European ancestry infants 8,321 European ancestry infants Affymetrix, Illumina [~ 2400000] (imputed) 3 infant head circumference http://www.ebi.ac.uk/efo/EFO_0004577 GCST001484 Genome-wide genotyping array 2012-04-18 22419666 Shi M 2012-03-14 Am J Med Genet A www.ncbi.nlm.nih.gov/pubmed/22419666 Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts. Orofacial clefts 1,094 European ancestry triads, 1,277 Asian ancestry triads, 87 triads NA Illumina [NR] 17 obsolete Mendelian syndromes with cleft lip/palate http://purl.obolibrary.org/obo/MONDO_0015335 GCST001442 Genome-wide genotyping array 2012-06-22 22558069 Osman W 2012-04-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/22558069 Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese. Non-albumin protein levels Up to 9,103 Japanese ancestry individuals Up to 1,629 Japanese ancestry individuals Illumina [2178644] (imputed) 5 serum non-albumin protein measurement http://www.ebi.ac.uk/efo/EFO_0004568 GCST001496 Genome-wide genotyping array 2012-08-20 22747683 Eriksson N 2012-06-30 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/22747683 Genetic variants associated with breast size also influence breast cancer risk. Breast size 16,175 European ancestry female individuals NA Illumina [7422970] (imputed) 38 breast size http://www.ebi.ac.uk/efo/EFO_0004884 GCST001585 Genome-wide genotyping array 2011-10-01 21896673 Chen D 2011-09-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21896673 Genome-wide association study of HPV seropositivity. HPV seropositivity 1,286 European ancestry lung cancer cases, 679 European ancestry head and neck cancer cases, 811 European ancestry kidney cancer cases, 2,035 European ancestry controls 1,307 Hispanic head and neck cancer cases, 1,037 Hispanic controls Illumina [316015] 1 HPV seropositivity http://www.ebi.ac.uk/efo/EFO_0004510 GCST001225 Genome-wide genotyping array 2010-12-09 20978177 Penney KL 2010-10-26 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/20978177 Genome-wide association study of prostate cancer mortality. Prostate cancer mortality 196 European ancestry lethal cases, 368 European ancestry long-term survivor cases 500 European ancestry lethal cases, 155 European ancestry long-term survivor cases Affymetrix [419613] 0 survival time, metastatic prostate cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000196 GCST000844 Genome-wide genotyping array 2011-10-11 21909110 Wain LV 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909110 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Blood pressure 74,064 European ancestry individuals 48,607 European ancestry individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 27 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST001236 Genome-wide genotyping array 2011-10-11 21909110 Wain LV 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909110 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Blood pressure 74,064 European ancestry individuals 48,607 European ancestry individuals Affymetrix, Illumina, Perlegen [NR] (imputed) 14 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST001235 Genome-wide genotyping array 2013-04-04 23319000 Luykx JJ 2013-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23319000 Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Metabolite levels (HVA/5-HIAA ratio) up to 398 European ancestry individuals NA Illumina [5767231] (imputed) 9 HVA measurement, 5-HIAA measurement http://www.ebi.ac.uk/efo/EFO_0005131, http://www.ebi.ac.uk/efo/EFO_0005132 GCST001818 Genome-wide genotyping array 2013-04-04 23319000 Luykx JJ 2013-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23319000 Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Metabolite levels (HVA-5-HIAA Factor score) up to 398 European ancestry individuals NA Illumina [5767231] (imputed) 12 HVA measurement, 5-HIAA measurement http://www.ebi.ac.uk/efo/EFO_0005131, http://www.ebi.ac.uk/efo/EFO_0005132 GCST001817 Genome-wide genotyping array 2013-04-04 23319000 Luykx JJ 2013-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23319000 Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Metabolite levels (HVA) up to 398 European ancestry individuals NA Illumina [5767231] (imputed) 13 HVA measurement http://www.ebi.ac.uk/efo/EFO_0005131 GCST001824 Genome-wide genotyping array 2013-04-04 23319000 Luykx JJ 2013-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23319000 Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Metabolite levels (5-HIAA) up to 398 European ancestry individuals NA Illumina [5767231] (imputed) 13 5-HIAA measurement http://www.ebi.ac.uk/efo/EFO_0005132 GCST001820 Genome-wide genotyping array 2013-04-04 23319000 Luykx JJ 2013-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23319000 Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Metabolite levels (MHPG) up to 398 European ancestry individuals NA Illumina [5767231] (imputed) 20 MHPG measurement http://www.ebi.ac.uk/efo/EFO_0005133 GCST001822 Genome-wide genotyping array 2013-04-04 23319000 Luykx JJ 2013-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23319000 Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Metabolite levels (5-HIAA/ MHPG Ratio) up to 398 European ancestry individuals NA Illumina [5767231] (imputed) 11 MHPG measurement, 5-HIAA measurement http://www.ebi.ac.uk/efo/EFO_0005133, http://www.ebi.ac.uk/efo/EFO_0005132 GCST001821 Genome-wide genotyping array 2013-04-04 23319000 Luykx JJ 2013-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23319000 Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid. Metabolite levels (HVA/MHPG ratio) up to 398 European ancestry individuals NA Illumina [5767231] (imputed) 25 HVA measurement, MHPG measurement http://www.ebi.ac.uk/efo/EFO_0005131, http://www.ebi.ac.uk/efo/EFO_0005133 GCST001823 Genome-wide genotyping array 2011-07-14 21685912 Hoglinger GU 2011-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21685912 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. Progressive supranuclear palsy 1,069 European ancestry cases, 2,958 European ancestry controls, 45 cases, 329 controls 1,051 European ancestry cases, 3,560 European ancestry controls Illumina [531451] 11 progressive supranuclear palsy http://purl.obolibrary.org/obo/MONDO_0019037 GCST001116 Genome-wide genotyping array 2013-10-18 20308991 Kim S 2010-03-23 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20308991 Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders. Brain cytoarchitecture 14 European ancestry bipolar cases, 15 European ancestry depression cases, 13 European ancestry schizophrenia cases, 14 European ancestry controls NA Affymetrix [309531] 2 prefrontal cortex cytoarchtiectural measurement http://www.ebi.ac.uk/efo/EFO_0006913 GCST000636 Genome-wide genotyping array 2009-06-01 19430480 Barrett JC 2009-05-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19430480 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. Type 1 diabetes 7,514 European ancestry cases, 9,045 European ancestry controls 4,267 European ancestry cases, 4,670 European ancestry controls, 4,342 European ancestry trios from 2,319 families Affymetrix, Illumina [841622] (imputed) 38 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000392 Genome-wide genotyping array 2010-09-23 20729852 Abnet CC 2010-08-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20729852 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. Esophageal cancer and gastric cancer 1,625 Chinese ancestry gastric cancer cases, 1,898 Chinese ancestry ESCC cases, 2,100 Chinese ancestry controls NA Illumina [551152] 4 esophageal carcinoma, gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0002916, http://www.ebi.ac.uk/efo/EFO_0000178 GCST000777 Genome-wide genotyping array 2010-09-14 20732627 Neale BM 2010-08-05 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/20732627 Case-control genome-wide association study of attention-deficit/hyperactivity disorder. Attention deficit hyperactivity disorder 896 European ancestry cases, 2,455 European ancestry controls Affymetrix [1033244] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST000757 Genome-wide genotyping array 2010-09-07 20662065 Clancy RM 2010-07-26 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/20662065 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. Neonatal lupus 116 European ancestry cases, 3,351 European ancestry controls NA Illumina [346110] 5 neonatal systemic lupus erythematosus http://www.ebi.ac.uk/efo/EFO_0004537 GCST000738 Genome-wide genotyping array 2012-09-12 22763476 Zhang D 2012-07-05 Hypertens Res www.ncbi.nlm.nih.gov/pubmed/22763476 Genome-wide linkage and association scans for pulse pressure in Chinese twins. Blood pressure 63 Chinese ancestry dizygotic twin pairs NA Affymetrix [~ 900000] 4 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST001598 Genome-wide genotyping array 2012-03-09 22306652 Bellenguez C 2012-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22306652 Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Stroke 3,548 European ancestry cases, 5,972 European ancestry controls 6,594 European ancestry cases, 34,864 European ancestry controls Illumina [495851] 1 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST001400 Genome-wide genotyping array 2010-09-11 20686651 Gudbjartsson DF 2010-07-29 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20686651 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. Chronic kidney disease and serum creatinine levels 1,689 European ancestry cases, 37,076 European ancestry controls 1,972 European ancestry cases, 6,125 European ancestry controls Illumina [~ 2500000] (imputed) 4 creatinine measurement, chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0003884 GCST000742 Genome-wide genotyping array 2012-06-18 22541561 Zhao H 2012-04-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22541561 A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia. Non-obstructive azoospermia 802 Han Chinese ancestry cases, 1,863 Han Chinese ancestry controls 1,424 Han Chinese ancestry cases, 2,713 Han Chinese ancestry controls Affymetrix, Illumina [912924] 1 azoospermia http://www.ebi.ac.uk/efo/EFO_0000279 GCST001494 Genome-wide genotyping array 2012-09-21 22843503 Qi Q 2012-07-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22843503 Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels. Resistin levels 3,248 European ancestry individuals 659 European ancestry individuals Affymetrix, Illumina [2543887] (imputed) 4 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST001620 Genome-wide genotyping array 2012-06-18 22513714 Shin J 2012-04-19 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22513714 Genetic architecture for susceptibility to gout in the KARE cohort study. Gout 520 Korean ancestry cases, 8,314 Korean ancestry controls NA Affymetrix [NR] (imputed) 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST001488 Genome-wide genotyping array 2013-07-31 23455636 Fritsche LG 2013-03-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23455636 Seven new loci associated with age-related macular degeneration. Age-related macular degeneration 6,713 European ancestry cases, 48,402 European ancestry contols, 110 Southern Indian ancestry cases, 119 Southern Indian ancestry controls, 827 Japanese ancestry cases, 3,323 Japanese ancestry controls 9,070 European ancestry cases, 7,683 European ancestry contols, 461 East Asian ancestry cases, 547 East Asian ancestry controls Affymetrix, Illumina [2442884] (imputed) 19 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST001884 Genome-wide genotyping array 2012-08-16 22693232 Zhou J 2012-06-12 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/22693232 A functional variation in CD55 increases the severity of 2009 pandemic H1N1 influenza A virus infection. Influenza (severity) 25 Chinese ancestry severe cases, 26 Chinese ancestry controls 152 Chinese ancestry severe cases, 222 Chinese ancestry controls Affymetrix [~ 1000000] 0 influenza http://www.ebi.ac.uk/efo/EFO_0007328 GCST001568 Genome-wide genotyping array 2010-09-11 20707712 Mosing MA 2010-08-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/20707712 A genome-wide association study of self-rated health. Self-rated health 6,706 European individuals from 2,585 independent families NA Illumina [2380486] (imputed) 10 self rated health http://www.ebi.ac.uk/efo/EFO_0004778 GCST000747 Genome-wide genotyping array 2012-09-20 22773346 Edwards DR 2012-07-07 Age (Dordr) www.ncbi.nlm.nih.gov/pubmed/22773346 Linkage and association of successful aging to the 6q25 region in large Amish kindreds. Aging 263 Amish individuals aged 80 years or older NA Affymetrix [630309] 8 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST001599 Genome-wide genotyping array 2012-08-10 23505185 Plourde M 2012-06-28 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/23505185 A variant in the LRRFIP1 gene is associated with adiposity and inflammation. Adiposity 928 French Canadian individuals NA Illumina [543714] 1 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001583 Genome-wide genotyping array 2012-09-18 22843499 Boraska V 2012-07-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22843499 Genome-wide meta-analysis of common variant differences between men and women. Sex ratio at birth 61,094 European ancestry female individuals, 53,769 European ancestry male individuals NA Affymetrix, Illumina [2623828] (imputed) 0 sex ratio http://www.ebi.ac.uk/efo/EFO_0004820 GCST001625 Genome-wide genotyping array 2012-07-13 22544364 Turnbull C 2012-04-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22544364 A genome-wide association study identifies susceptibility loci for Wilms tumor. Wilms tumor 757 European ancestry cases, 1,879 European ancestry controls 1,488 European ancestry cases, 3,851 European ancestry controls Illumina [599255] 7 Nephroblastoma http://www.orpha.net/ORDO/Orphanet_654 GCST001500 Genome-wide genotyping array 2013-02-23 23275298 Fox ER 2012-12-28 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23275298 Genome-wide association study of cardiac structure and systolic function in African Americans: the Candidate Gene Association Resource (CARe) study. Cardiac structure and function 6,765 African American individuals 2,468 African American individuals, 12,612 European ancestry individuals Affymetrix [~ 2500000] (imputed) 0 cardiovascular measurement http://www.ebi.ac.uk/efo/EFO_0004298 GCST001797 Genome-wide genotyping array 2011-01-04 21048783 Kamada F 2010-11-04 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21048783 A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. Moyamoya disease 72 Japanese ancestry cases, 45 Japanese ancestry controls 63 Japanese ancestry cases, 45 Japanese ancestry controls Illumina [785720] 1 Moyamoya disease http://purl.obolibrary.org/obo/MONDO_0016820 GCST000860 Genome-wide genotyping array 2013-04-12 22075249 Tang WH 2011-11-10 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/22075249 Clinical and genetic association of serum ceruloplasmin with cardiovascular risk. Serum ceruloplasmin levels 2,647 European ancestry individuals 2,050 European ancestry individuals Affymetrix [2421770] (imputed) 1 serum ceruloplasmin measurement http://www.ebi.ac.uk/efo/EFO_0005139 GCST001318 Genome-wide genotyping array 2011-12-20 22118420 Datta S 2011-11-28 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/22118420 A genome-wide search for non-UGT1A1 markers associated with unconjugated bilirubin level reveals significant association with a polymorphic marker near a gene of the nucleoporin family. Bilirubin levels 182 South Asian ancestry individuals NA Illumina [512349] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST001333 Genome-wide genotyping array 2013-08-02 23544013 Couch FJ 2013-03-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23544013 Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. Ovarian cancer in BRCA1 mutation carriers 683 European ancestry cases, 2,044 European ancestry controls 1,706 European ancestry cases, 10,258 European ancestry controls Illumina [2568349] (imputed) 7 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST001917 Genome-wide genotyping array 2013-08-02 23544013 Couch FJ 2013-03-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23544013 Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk. Breast Cancer in BRCA1 mutation carriers 1,426 European ancestry cases, 1,301 European ancestry controls 6,031 European ancestry cases, 5,933 European ancestry controls Illumina [2568349] (imputed) 6 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001916 Genome-wide genotyping array 2013-07-31 23534349 Jeff JM 2013-03-28 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23534349 Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. QT interval 455 African American individuals NA Illumina [> 930000] 8 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST001922 Genome-wide genotyping array 2013-07-31 23534349 Jeff JM 2013-03-28 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23534349 Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. Heart rate 455 African American individuals NA Illumina [> 930000] 5 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST001921 Genome-wide genotyping array 2013-07-31 23534349 Jeff JM 2013-03-28 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23534349 Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. PR interval 455 African American individuals NA Illumina [> 930000] 9 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST001925 Genome-wide genotyping array 2013-07-31 23534349 Jeff JM 2013-03-28 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23534349 Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans. QRS duration 455 African American individuals NA Illumina [> 930000] 9 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST001920 Genome-wide genotyping array 2010-06-22 20522523 Kasperaviciute D 2010-06-03 Brain www.ncbi.nlm.nih.gov/pubmed/20522523 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. Partial epilepsies Up to 3,445 European ancestry cases, 6,935 European ancestry controls NA Illumina [528745] 6 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST000691 Genome-wide genotyping array 2009-03-28 19270707 Birnbaum S 2009-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19270707 Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. Orofacial clefts 224 European ancestry cases, 383 European ancestry controls 246 cases, 954 controls Illumina [521176] 2 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST000353 Genome-wide genotyping array 2012-09-26 22843504 Anney R 2012-07-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22843504 Individual common variants exert weak effects on the risk for autism spectrum disorders. Autism 1,419 European ancestry cases from 1416 families 1,314 European ancestry cases from 1301 families Illumina [947233] 4 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST001619 Genome-wide genotyping array 2012-11-29 23000144 Nakamura M 2012-09-18 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23000144 Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population. Primary biliary cholangitis 487 Japanese ancestry cases, 476 Japanese ancestry controls 787 Japanese ancestry cases, 615 Japanese ancestry controls Affymetrix [421245] 7 biliary liver cirrhosis http://www.ebi.ac.uk/efo/EFO_0004267 GCST001685 Genome-wide genotyping array 2012-07-11 22561518 Jin Y 2012-05-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22561518 Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. Vitiligo 418 European ancestry cases, 2,810 European ancestry controls 1,377 European ancestry cases, 1,284 European ancestry controls Illumina [495821] 14 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST001509 Genome-wide genotyping array 2013-07-01 23508960 Zhou G 2013-03-18 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/23508960 Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2). Aspirin hydrolysis (plasma) 2,054 European ancestry individuals Affymetrix [2421779] (imputed) 1 aspirin hydrolysis measurement http://www.ebi.ac.uk/efo/EFO_0005211 GCST001910 Genome-wide genotyping array 2012-11-22 22699663 Divaris K 2012-07-01 J Dent Res www.ncbi.nlm.nih.gov/pubmed/22699663 Genome-wide association study of periodontal pathogen colonization. Periodontal microbiota 1,020 European ancestry individuals NA Affymetrix [~ 2500000] (imputed) 16 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST001588 Genome-wide genotyping array 2012-08-14 22832964 David SP 2012-05-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/22832964 Genome-wide meta-analyses of smoking behaviors in African Americans. Smoking behavior Up to 32,389 African American individuals NA Affymetrix, Illumina [~ 2900000] (imputed) 5 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST001539 Genome-wide genotyping array 2013-03-06 23247145 Makela KM 2012-12-17 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23247145 Genome-wide association study pinpoints a new functional apolipoprotein B variant influencing oxidized low-density lipoprotein levels but not cardiovascular events: AtheroRemo Consortium. LDL (oxidized) 2,080 European ancestry individuals 4,238 European ancestry individuals Illumina [2543887] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST001777 Genome-wide genotyping array 2012-12-05 23001564 Mangino M 2012-09-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23001564 Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans. Telomere length 9,190 European ancestry individuals 2,226 individuals Affymetrix, Illumina [~ 2500000] (imputed) 4 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST001697 Genome-wide genotyping array 2013-08-10 23548203 Zhang M 2013-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23548203 Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. Sunburns 9,283 European ancestry individuals 4,236 European ancestry individuals Affymetrix, Illumina [7588169] (imputed) 4 sunburn http://www.ebi.ac.uk/efo/EFO_0003958 GCST001933 Genome-wide genotyping array 2013-08-10 23548203 Zhang M 2013-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23548203 Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. Eye color 3871 European ancestry individuals 2,496 European ancestry individuals Affymetrix, Illumina [2469762] (imputed) 8 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST001929 Genome-wide genotyping array 2013-08-10 23548203 Zhang M 2013-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23548203 Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. Hair color 7,070 European ancestry individuals 4,155 European ancestry individuals Affymetrix, Illumina [7588169] (imputed) 6 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST001932 Genome-wide genotyping array 2013-08-10 23548203 Zhang M 2013-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23548203 Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. Non-melanoma skin cancer 6,747 European ancestry individuals 2,078 European ancestry individuals Affymetrix, Illumina [7588169] (imputed) 4 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST001940 Genome-wide genotyping array 2013-08-10 23548203 Zhang M 2013-04-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23548203 Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans. Tanning 9,678 European ancestry individuals Affymetrix, Illumina [7588169] (imputed) 5 suntan http://www.ebi.ac.uk/efo/EFO_0004279 GCST001939 Genome-wide genotyping array 2013-09-05 23626673 Matullo G 2013-04-23 PLoS One www.ncbi.nlm.nih.gov/pubmed/23626673 Genetic variants associated with increased risk of malignant pleural mesothelioma: a genome-wide association study. Malignant pleural mesothelioma 392 European ancestry cases, 367 European ancestry controls 428 European ancestry cases, 1,269 European ancestry controls Illumina [5000000] (imputed) 0 malignant pleural mesothelioma http://www.ebi.ac.uk/efo/EFO_0000770 GCST001978 Genome-wide genotyping array 2013-07-25 23555300 Cui J 2013-03-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23555300 Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. Response to anti-TNF therapy in rheumatoid arthritis Up to 2,706 European ancestry cases NA Affymetrix, Illumina [~ 2000000] (imputed) 4 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST001927 Genome-wide genotyping array 2013-07-25 23555300 Cui J 2013-03-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23555300 Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis. Response to anti-TNF therapy in rheumatoid arthritis 733 European ancestry cases 139 European ancestry cases, 151 Japanese ancestry cases Illumina [~ 2000000] (imputed) 1 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST001926 Genome-wide genotyping array 2012-10-09 22890011 Frazier-Wood AC 2012-08-09 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/22890011 Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate. Response to fenofibrate 817 European ancestry individuals NA Affymetrix [~ 2543887] (imputed) 10 response to fenofibrate http://purl.obolibrary.org/obo/GO_1901557 GCST001632 Genome-wide genotyping array 2013-04-09 23290196 Hek K 2013-01-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23290196 A genome-wide association study of depressive symptoms. Depression (quantitative trait) up to 34,549 European ancestry individuals up to 16,709 European ancestry individuals Affymetrix, Illumina [2391896] (imputed) 2 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST001802 Genome-wide genotyping array 2013-03-27 23300278 Saxena R 2013-01-08 Diabetes www.ncbi.nlm.nih.gov/pubmed/23300278 Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. Type 2 diabetes 842 Punjabi Sikh ancestry cases, 774 Punjabi Sikh ancestry controls up to 2,512 Punjabi Sikh ancestry cases and 3,201 Punjabi Sikh ancestry controls, up to 16,128 South Asian ancestry cases and 23,846 South Asian ancestry controls, up to 16,746 East Asian ancestry cases and 16,961 East Asian ancestry controls, up to 8,130 European ancestry cases and 38,987 European ancestry controls Illumina [1232008] (imputed) 17 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001809 Genome-wide genotyping array 2013-11-09 23666240 Ruark E 2013-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23666240 Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14. Testicular germ cell tumor 986 European ancestry cases, 4,946 European ancestry controls 1,064 European ancestry cases, 10,082 European ancestry controls Illumina [307291] 15 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST002022 Genome-wide genotyping array 2012-04-18 22430674 Lambert JC 2012-03-20 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22430674 Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Alzheimer's disease 2,025 European ancestry cases, 5,328 European ancestry controls 7,913 European ancestry cases, 10,417 European ancestry controls Illumina [287956] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001449 Genome-wide genotyping array 2012-01-04 22140272 Dalgaard MD 2011-12-03 J Med Genet www.ncbi.nlm.nih.gov/pubmed/22140272 A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation. Testicular dysgenesis syndrome 488 European ancestry male cases, 439 European ancestry male controls 436 European ancestry male cases, 235 European ancestry male controls Affymetrix [600798] 0 testicular dysgenesis syndrome http://www.ebi.ac.uk/efo/EFO_0004893 GCST001344 Genome-wide genotyping array 2013-05-02 23364009 Yang X 2013-01-30 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/23364009 Common variants at 12q24 are associated with drinking behavior in Han Chinese. Drinking behavior 1,420 Han Chinese ancestry cases, 3,590 Han Chinese ancestry controls 4,896 Han Chinese ancestry cases, 13,293 Han Chinese ancestry controls Affymetrix [~ 2200000] (imputed) 1 drinking behavior http://www.ebi.ac.uk/efo/EFO_0004315 GCST001842 Genome-wide genotyping array 2011-11-18 22001757 Chambers JC 2011-10-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22001757 Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Liver enzyme levels (alanine transaminase) Up to 52,350 European ancestry individuals, up to 8,739 Indian Asian ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 4 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST001275 Genome-wide genotyping array 2011-11-18 22001757 Chambers JC 2011-10-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22001757 Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Liver enzyme levels (alkaline phosphatase) Up to 52,350 European ancestry individuals, up to 8,739 Indian Asian ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 14 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST001276 Genome-wide genotyping array 2011-11-18 22001757 Chambers JC 2011-10-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22001757 Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma. Liver enzyme levels (gamma-glutamyl transferase) Up to 52,350 European ancestry individuals, up to 8,739 Indian Asian ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 26 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST001277 Genome-wide genotyping array 2012-12-04 22990015 Arning A 2012-09-20 Blood www.ncbi.nlm.nih.gov/pubmed/22990015 A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke. Stroke (pediatric) 270 European ancestry trios NA Illumina [334581] 4 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST001689 Genome-wide genotyping array 2011-06-03 21602798 Haiman CA 2011-05-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21602798 Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21. Prostate cancer 3,425 African American cases, 3,290 African American controls 1,500 African American/Afro-Caribbean cases, 1,908 African American/Afro-Caribbean controls, 344 Sub-Saharan African ancestry cases, 1,361 Sub-Saharan African ancestry controls Illumina [10471986] 1 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001078 Genome-wide genotyping array 2013-01-08 23041938 Lee YJ 2012-10-06 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/23041938 Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. Behcet's disease 367 Korean ancestry cases, 800 Korean ancestry controls 363 Japanese ancestry cases, 272 Japanese ancestry controls Affymetrix [594591] 0 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST001707 Genome-wide genotyping array 2011-11-04 21977987 Trompet S 2011-10-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/21977987 Replication of LDL GWAs hits in PROSPER/PHASE as validation for future (pharmaco)genetic analyses. LDL cholesterol 5,244 European ancestry individuals 10,754 individuals Illumina [2500000] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST001262 Genome-wide genotyping array 2012-04-06 22432041 Johnson MP 2012-03-14 PLoS One www.ncbi.nlm.nih.gov/pubmed/22432041 Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. Preeclampsia 538 European ancestry cases, 540 European ancestry controls 1,894 European ancestry cases, 3,022 European ancestry controls Illumina [648175] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST001443 Genome-wide genotyping array 2012-12-06 23007406 Yang JJ 2012-09-24 Blood www.ncbi.nlm.nih.gov/pubmed/23007406 Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia. Acute lymphoblastic leukemia (childhood) 1,268 European, South Asian, East Asian, African American/Afro-Caribbean, Hispanic and other ancestry cases 1,267 European, South Asian, East Asian, African American/Afro-Caribbean, Hispanic and other ancestry cases Affymetrix [444044] 10 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST001693 Genome-wide genotyping array 2012-12-16 23001997 Hou S 2012-12-06 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/23001997 Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. Behcet's disease 147 Han Chinese ancestry cases, 951 Han Chinese ancestry controls 554 Han Chinese ancestry cases, 1,159 Han Chinese ancestry controls Affymetrix [661736] 6 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST001768 Genome-wide genotyping array 2012-04-03 22428042 Nakano M 2012-03-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/22428042 Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese. Glaucoma (primary open-angle) 833 Japanese ancestry cases, 686 Japanese ancestry controls 411 Japanese ancestry cases, 289 Japanese ancestry controls Affymetrix [653519] 1 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST001441 Genome-wide genotyping array 2013-01-11 23118974 Candille SI 2012-10-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/23118974 Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations. Eye color 175 European ancestry individuals 293 European ancestry individuals Illumina [313763] 3 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST001723 Genome-wide genotyping array 2011-07-13 21700265 Kullo IJ 2011-06-22 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21700265 Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. Erythrocyte sedimentation rate 1,979 European ancestry individuals 5,628 European ancestry individuals Illumina [476395] 5 blood sedimentation http://www.ebi.ac.uk/efo/EFO_0004304 GCST001120 Genome-wide genotyping array 2010-03-06 20150558 He M 2010-02-11 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/20150558 Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. Interleukin-18 levels 1,523 European ancestry female individuals 435 European ancestry female individuals Affymetrix [704409] 2 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST000590 Genome-wide genotyping array 2011-03-01 21248740 Simon-Sanchez J 2011-01-19 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21248740 Genome-wide association study confirms extant PD risk loci among the Dutch. Parkinson's disease 772 European ancestry cases, 2,024 European ancestry controls NA Illumina [514799] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000950 Genome-wide genotyping array 2013-07-01 23493294 Gao X 2013-03-14 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/23493294 A genome-wide association study of central corneal thickness in Latinos. Central corneal thickness 1,644 Latino individuals 124 Latino individuals Illumina [6290547] (imputed) 2 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST001903 Genome-wide genotyping array 2012-01-14 22156575 Paus T 2011-12-09 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/22156575 KCTD8 gene and brain growth in adverse intrauterine environment: a genome-wide association study. Brain development 557 French Canadian female adolescent individuals 2,601 European ancestry adolescent individuals Illumina [530011] 0 infant head circumference http://www.ebi.ac.uk/efo/EFO_0004577 GCST001349 Genome-wide genotyping array 2012-05-10 22479202 Dastani Z 2012-03-29 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22479202 Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Adiponectin levels 29,347 European ancestry individuals, 4,232 African American individuals, 1,776 Filipino ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 10 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST001463 Genome-wide genotyping array 2012-05-10 22479202 Dastani Z 2012-03-29 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22479202 Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Adiponectin levels 29,347 European ancestry individuals 10,536 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 21 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST001465 Genome-wide genotyping array 2012-07-19 22544366 Ellinor PT 2012-04-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22544366 Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Atrial fibrillation 6,707 European ancestry cases, 52,426 European ancestry controls 5,381 European ancestry casses, 10,030 European ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 10 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST001499 Genome-wide genotyping array 2012-06-22 22558097 Milton JN 2012-04-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/22558097 A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia. Cholelithiasis-related traits in sickle cell anemia 905 African American cases 2,152 African American cases Illumina [569615] 1 cholelithiasis, bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004799, http://www.ebi.ac.uk/efo/EFO_0004570 GCST001497 Genome-wide genotyping array 2011-07-20 21740922 Nebel A 2011-06-29 Mech Ageing Dev www.ncbi.nlm.nih.gov/pubmed/21740922 A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals. Longevity 763 European ancestry individuals, 1,058 European ancestry individuals 754 European ancestry individuals, 860 European ancestry individuals Affymetrix [664472] 1 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST001131 Genome-wide genotyping array 2011-10-29 21961650 Squassina A 2011-10-03 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/21961650 Evidence for association of an ACCN1 gene variant with response to lithium treatment in Sardinian patients with bipolar disorder. Response to lithium treatment in bipolar disorder 26 European ancestry lithium treatment responders, 26 European ancestry lithium treatment non-responders 34 European ancestry lithium treatment responders, 118 European ancestry lithium treatment non-responders Affymetrix [645148] 0 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST001259 Genome-wide genotyping array 2012-07-27 22675492 Prescott J 2012-06-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/22675492 Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women. Sex hormone-binding globulin levels 1,598 European ancestry female individuals NA Illumina [~ 2500000] (imputed) 8 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST001554 Genome-wide genotyping array 2012-07-27 22675492 Prescott J 2012-06-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/22675492 Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women. Estradiol levels 1,583 European ancestry female individuals NA Illumina [~ 2500000] (imputed) 8 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST001553 Genome-wide genotyping array 2012-07-27 22675492 Prescott J 2012-06-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/22675492 Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women. Testosterone levels 1,589 European ancestry female individuals NA Illumina [~ 2500000] (imputed) 5 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST001555 Genome-wide genotyping array 2008-09-12 18711365 Ferreira MA 2008-08-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18711365 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. Bipolar disorder 4,387 European ancestry cases, 6,209 European ancestry controls NA Affymetrix [1769948] (imputed) 21 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000220 Genome-wide genotyping array 2010-08-18 20622878 Remmers EF 2010-07-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20622878 Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. Behcet's disease 1,215 Turkish ancestry cases, 1,278 Turkish ancestry controls Up to 111 Turkish ancestry cases, 225 Turkish ancestry controls, 189 Middle Eastern Arab ancestry cases, 163 Middle Eastern Arab ancestry controls, 227 European ancestry cases, 203 European ancestry controls, 688 East Asian ancestry cases, 791 East Asian ancestry controls Illumina [311459] 2 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST000726 Genome-wide genotyping array 2011-07-27 21738484 Smith EN 2011-06-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21738484 Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. Bipolar disorder 1,190 European and unknown ancestry cases, 401 European and unknown ancestry controls 16,179 individuals Affymetrix [703019] 6 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001135 Genome-wide genotyping array 2013-08-29 23646285 Khor SS 2013-04-16 PeerJ www.ncbi.nlm.nih.gov/pubmed/23646285 Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia. Hypersomnia (HLA-DQB1*06:02 negative) 125 Japanese ancestry cases, 562 Japanese ancestry controls Affymetrix [508366] (imputed) 5 hypersomnia http://www.ebi.ac.uk/efo/EFO_0005246 GCST001971 Genome-wide genotyping array 2011-11-03 21971053 Takeuchi F 2011-10-05 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21971053 Genome-wide association study of coronary artery disease in the Japanese. Coronary heart disease 806 Japanese ancestry cases, 1,337 Japanese ancestry controls 3,593 Japanese ancestry cases, 6,335 Japanese ancestry controls Illumina [451382] 3 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001260 Genome-wide genotyping array 2011-08-17 21747397 Rietschel M 2011-07-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21747397 Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Schizophrenia 1,169 European ancestry cases, 3,714 European ancestry controls 7,303 European ancestry cases, 26,274 European ancestry controls Illumina [475427] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001152 Genome-wide genotyping array 2012-07-25 22665904 Willis JA 2012-06-04 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/22665904 A replication study and genome-wide scan of single-nucleotide polymorphisms associated with pancreatic cancer risk and overall survival. Pancreatic cancer 252 European ancestry cases 798 European ancestry cases, 21 African American cases, 10 East Asian ancestry cases, 4 Asian Indian ancestry cases Illumina [301250] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST001556 Genome-wide genotyping array 2012-06-27 22570697 Matesanz F 2012-05-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/22570697 Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1. Multiple sclerosis 2,127 European ancestry cases, 4,558 European ancestry controls 2,785 European ancestry cases, 2,940 European ancestry controls Affymetrix, Illumina [130903] 1 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST001505 Genome-wide genotyping array 2012-07-19 22648509 Wang KS 2012-05-31 J Mol Neurosci www.ncbi.nlm.nih.gov/pubmed/22648509 PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies. Formal thought disorder in schizophrenia 835 European ancestry cases, 2,694 European ancestry controls NA Affymetrix [729454] 5 formal thought disorder http://www.ebi.ac.uk/efo/EFO_0004805 GCST001549 Genome-wide genotyping array 2008-06-16 17463248 Scott LJ 2007-04-26 Science www.ncbi.nlm.nih.gov/pubmed/17463248 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. Type 2 diabetes 1,161 European ancestry cases, 1,174 European ancestry controls 1,215 European ancestry cases, 1,258 European ancestry controls Illumina [315635] 10 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000024 Genome-wide genotyping array 2013-03-11 23242368 Jiang DK 2012-12-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23242368 Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. Hepatocellular carcinoma in hepatitis B infection 1,161 Chinese ancestry cases, 1,353 Chinese ancestry controls 4,319 Chinese ancestry cases, 4,966 Chinese ancestry controls Illumina [1672517] (imputed) 2 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST001775 Genome-wide genotyping array 2013-06-11 23455637 Iles MM 2013-03-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23455637 A variant in FTO shows association with melanoma risk not due to BMI. Melanoma 1,353 European ancestry cases, 3,566 European ancestry controls 12,313 European ancestry cases, Up to 55,667 European ancestry controls Illumina [2600000] (imputed) 1 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST001886 Genome-wide genotyping array 2013-06-11 23459936 Divaris K 2013-03-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23459936 Exploring the genetic basis of chronic periodontitis: a genome-wide association study. Periodontitis 4,504 European ancestry individuals 656 European ancestry and African American individuals Affymetrix [2135236] (imputed) 3 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST001888 Genome-wide genotyping array 2011-07-20 21738487 Do CB 2011-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21738487 Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. Parkinson's disease 3,426 European ancestry cases, 29,624 European ancestry controls NA Illumina [522782] 11 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST001126 Genome-wide genotyping array 2012-06-27 22551897 Mahasirimongkol S 2012-05-03 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22551897 Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis. Tuberculosis 433 Thai ancestry cases, 295 Thai ancestry controls, 188 Japanese ancestry cases, 934 Japanese ancestry controls 369 Thai ancestry cases, 439 Thai ancestry controls, 112 Japanese ancestry cases, 1,089 Japanese ancestry controls Illumina [533252] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST001504 Genome-wide genotyping array 2015-05-29 21323541 Stanescu HC 2011-02-22 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/21323541 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. Idiopathic membranous nephropathy 556 European ancestry cases, 2,338 European ancestry controls NA Illumina [242824] 21 membranous glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004254 GCST000984 Genome-wide genotyping array 2013-03-27 23291587 Kirino Y 2013-01-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23291587 Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1. Behcet's disease 435 Turkish uveitis cases, 780 Turkish without uveitis cases, 1,278 Turkish controls 355 Turkish uveitis cases, 483 Turkish without uveitis cases, 601 Turkish controls, up to 612 Japanese ancestry cases, up to 740 Japanese ancestry controls Illumina [779465] (imputed) 6 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST001804 Genome-wide genotyping array 2012-04-03 22420046 Stergiakouli E 2012-02-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/22420046 Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD. Attention deficit hyperactivity disorder 727 European ancestry children, 5,081 European ancestry individuals 1,142 European ancestry individuals, 896 cases and 2,455 controls from 2,064 trios Illumina [502702] 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST001395 Genome-wide genotyping array 2013-06-14 23459443 Avery CL 2013-03-05 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/23459443 Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval. QT interval (drug interaction) 33,781 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 17 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST001890 Genome-wide genotyping array 2012-08-15 22672568 Heit JA 2012-06-05 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/22672568 A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. Venous thromboembolism 1,503 European and other ancestry cases, 1,459 European and other ancestry controls 1,407 cases, 1,418 controls Illumina [~ 2500000] (imputed) 5 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST001557 Genome-wide genotyping array 2011-07-21 21738478 Okada Y 2011-06-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21738478 Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. White blood cell types 8,794 Japanese ancestry individuals 5,998 Japanese ancestry individuals Illumina [2178645] (imputed) 20 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST001134 Genome-wide genotyping array 2011-11-09 22001756 Khor CC 2011-10-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22001756 Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1. Dengue shock syndrome 2,008 Vietnamese ancestry child cases, 2,018 Vietnamese ancestry child controls 1,737 Vietnamese ancestry child cases, 2,934 Vietnamese ancestry child controls Illumina [481342] 4 Dengue Hemorrhagic Fever http://www.ebi.ac.uk/efo/EFO_0004227 GCST001278 Genome-wide genotyping array 2012-04-17 22426144 Long J 2012-03-16 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/22426144 Genome-wide association study identifies a possible susceptibility locus for endometrial cancer. Endometrial cancer 832 Chinese ancestry cases, 2,682 Chinese ancestry controls 6,864 European ancestry cases, 12,936 European ancestry controls, 796 Chinese ancestry cases, 978 Chinese ancestry controls Affymetrix [585963] 0 endometrial neoplasm http://www.ebi.ac.uk/efo/EFO_0004230 GCST001447 Genome-wide genotyping array 2013-01-09 23041239 Traylor M 2012-10-05 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/23041239 Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies. Stroke (ischemic) 12,389 European ancestry cases, 62,004 European ancestry controls 1,322 Pakistani ancestry cases, 1,143 Pakistani ancestry controls, 12,025 European ancestry cases, 27,940 European ancestry controls Affymetrix, Illumina [NR] (imputed) 8 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST001706 Genome-wide genotyping array 2012-11-05 22952603 Hart AB 2012-08-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/22952603 Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13). Response to amphetamines 1 American Indian ancestry individual, 18 African American individuals, 10 Asian ancestry individuals, 325 European ancestry individuals, 17 Hispanic individuals, 10 individuals NA Affymetrix [5476100] (imputed) 89 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST001651 Genome-wide genotyping array 2008-06-20 18483556 Han J 2008-05-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/18483556 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. Black vs. blond hair color 2,287 European ancestry female individuals 8,465 European ancestry individuals Illumina [528173] 7 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST000190 Genome-wide genotyping array 2008-07-01 18483556 Han J 2008-05-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/18483556 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. Black vs. red hair color 2,287 European ancestry female individuals 8,465 European ancestry individuals Illumina [528173] 7 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST000191 Genome-wide genotyping array 2011-11-15 22006218 Yoon D 2011-10-18 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22006218 Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence. Smoking behavior 8,842 Korean ancestry individuals 1,366 African American individuals, 671 European ancestry individuals Affymetrix [352228] 6 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST001286 Genome-wide genotyping array 2009-09-09 19706858 Shuldiner AR 2009-08-26 JAMA www.ncbi.nlm.nih.gov/pubmed/19706858 Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. Response to clopidogrel therapy 429 Amish individuals 140 European ancestry individuals, 83 African American individuals, 4 individuals Affymetrix [400230] 1 response to platelet aggregation inhibitor http://purl.obolibrary.org/obo/GO_0061478 GCST000467 Genome-wide genotyping array 2012-04-03 22423221 Qayyum R 2012-03-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22423221 A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. Mean platelet volume 16,388 African American individuals NA Affymetrix, Illumina [~ 2200000] (imputed) 3 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST001439 Genome-wide genotyping array 2019-07-02 22423221 Qayyum R 2012-03-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22423221 A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. Platelet count 16,388 African American individuals NA Affymetrix, Illumina [~ 2200000] (imputed) 10 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST008047 Genome-wide genotyping array 2012-11-28 23028356 Myouzen K 2012-09-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23028356 Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese. Rheumatoid arthritis 2,303 Japanese ancestry cases, 3,380 Japanese ancestry controls 5,604 Japanese ancestry cases, 31,982 Japanese ancestry controls Illumina [NR] 2 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST001681 Genome-wide genotyping array 2012-12-21 23043469 Menzel S 2012-10-09 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/23043469 HbA2 levels in normal adults are influenced by two distinct genetic mechanisms. HbA2 levels 2,322 European ancestry individuals 1,716 European ancestry individuals Illumina [531038] 2 hemoglobin A2 measurement http://www.ebi.ac.uk/efo/EFO_0005845 GCST001710 Genome-wide genotyping array 2013-05-26 23455491 Zuo L 2013-02-27 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/23455491 NKAIN1-SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent. Alcohol dependence 1,409 European ancestry cases, 1,518 European ancestry controls 6,438 European ancestry individuals from 1,645 affected families Illumina [805814] 1 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001874 Genome-wide genotyping array 2013-08-28 23592221 Rahmani M 2013-04-16 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/23592221 Shared genetic factors for age at natural menopause in Iranian and European women. Menopause (age at onset) 165 Iranian ancestry early menopause females, 187 Iranian ancestry late menopause females 573 Iranian ancestry females, 38,968 European ancestry females Illumina [694326] 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST001970 Genome-wide genotyping array 2013-03-15 23263486 Kottgen A 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263486 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Urate levels 49,825 European ancestry males, 60,522 European ancestry females Up to 32,813 European ancestry individuals Affymetrix, Illumina, Perlegen [2450547] (imputed) 47 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST001791 Genome-wide genotyping array 2013-03-15 23263486 Kottgen A 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263486 Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Gout 2,115 European ancestry cases, 67,259 European ancestry controls 1,036 European ancestry cases Affymetrix, Illumina [2538056] (imputed) 6 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST001790 Genome-wide genotyping array 2011-07-08 21706003 Kilpelainen TO 2011-06-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21706003 Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. Adiposity 29,069 European ancestry individuals, 7,557 Indian Asian ancestry individuals 39,576 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 3 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001128 Genome-wide genotyping array 2013-06-18 23471985 Jahanshad N 2013-03-05 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/23471985 Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity. Brain connectivity 331 European ancestry individuals Illumina [428287] 12 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST001889 Genome-wide genotyping array 2013-02-26 23259602 Wang X 2012-12-21 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/23259602 Genome-wide association scan of dental caries in the permanent dentition. Dental caries 1,483 European ancestry comparatively younger individuals, 5,960 European ancestry comparatively older individuals NA Affymetrix, Illumina [~ 1400000] (imputed) 34 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST001786 Genome-wide genotyping array 2013-02-23 23255317 Wooten EC 2012-12-19 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23255317 Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy. Hypertrophic cardiomyopathy 174 European ancestry cases, 823 European ancestry controls 1,012 European ancestry cases, 1,326 European ancestry controls Illumina [311399] 0 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST001778 Genome-wide genotyping array 2013-06-26 23518928 Liu M 2013-03-21 Mol Endocrinol www.ncbi.nlm.nih.gov/pubmed/23518928 TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression. Estradiol plasma levels (breast cancer) 700 European ancestry cases, 50 African ancestry cases, 17 Asian ancestry cases, 5 American Indian ancestry cases NA Illumina [563945] 18 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST001914 Genome-wide genotyping array 2011-11-12 22004975 Li R 2011-10-17 Lupus www.ncbi.nlm.nih.gov/pubmed/22004975 Association of CD247 with systemic lupus erythematosus in Asian populations. Systemic lupus erythematosus 612 Chinese ancestry cases, 2,193 Chinese ancestry controls 2,866 East Asian ancestry cases, up to 4,808 East Asian ancestry controls, 473 Thai ancestry cases, up to 970 Thai ancestry controls Illumina [NR] 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST001279 Genome-wide genotyping array 2011-07-20 21706340 Teerlink C 2011-06-26 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21706340 A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q. Melanoma 156 European ancestry cases from 34 high-risk families, 2,150 European ancestry controls NA Illumina [491227] 1 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST001129 Genome-wide genotyping array 2013-02-19 23266556 Peters U 2012-12-21 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/23266556 Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis. Colorectal cancer 12,696 European ancestry colorectal tumor cases, 15,113 European ancestry controls 958 European ancestry colorectal tumor cases, 909 European ancestry controls, up to 2,098 East Asian ancestry colorectal tumor cases, up to 5,749 East Asian ancestry controls Affymetrix, Illumina [2708280] (imputed) 15 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST001787 Genome-wide genotyping array 2010-09-10 20663923 Anney R 2010-07-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20663923 A genome-wide scan for common alleles affecting risk for autism. Autism 1,230 European ancestry child cases from 1,217 families, 155 African American Asian or Latino child cases from 152 families, 1,880 controls 783 European ancestry child cases from 440 families, 303 child cases from 155 families, 1,965 European, African American and other ancestry controls Illumina [842348] 2 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST000740 Genome-wide genotyping array 2015-05-14 22005930 Hollingworth P 2011-10-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22005930 Genome-wide association study of Alzheimer's disease with psychotic symptoms. Psychosis and Alzheimer's disease 1,039 European ancestry cases with psychosis, 5,659 European ancestry controls, 260 European, African American and Native American ancestry cases with psychosis from 264 families NA Illumina [1847262] (imputed) 11 Alzheimer disease, psychotic symptoms http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0005940 GCST001285 Genome-wide genotyping array 2015-05-14 22005930 Hollingworth P 2011-10-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22005930 Genome-wide association study of Alzheimer's disease with psychotic symptoms. Psychosis in Alzheimer's disease 1,039 European ancestry cases with psychosis, 610 European ancestry cases without psychosis, 260 European, African American and Native American ancestry cases with psychosis and 125 European, African American and Native American ancestry cases without psychosis from 264 families NA Illumina [1882172] (imputed) 8 psychotic symptoms http://www.ebi.ac.uk/efo/EFO_0005940 GCST001282 Genome-wide genotyping array 2012-12-07 23028483 Ramasamy A 2012-09-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/23028483 Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA. Asthma 1,716 European ancestry cases, 16,888 European ancestry controls 4,035 European ancestry cases, 11,251 European ancestry controls Affymetrix, Illumina [~ 2200000] (imputed) 2 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001701 Genome-wide genotyping array 2013-01-11 23118916 Yang M 2012-10-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/23118916 Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population. IgM levels 1,999 Han Chinese ancestry individuals 1,496 East Asian ancestry individuals Illumina [1940243] (imputed) 3 serum IgM measurement http://www.ebi.ac.uk/efo/EFO_0004993 GCST001724 Genome-wide genotyping array 2012-07-13 22628180 Luciano M 2012-05-24 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/22628180 Genome-wide association uncovers shared genetic effects among personality traits and mood states. Personality dimensions 6,268 European ancestry individuals 9,244 European ancestry individuals Illumina [~ 2500000] (imputed) 0 personality trait http://www.ebi.ac.uk/efo/EFO_0004365 GCST001541 Genome-wide genotyping array 2008-06-22 18454148 Loos RJ 2008-05-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18454148 Common variants near MC4R are associated with fat mass, weight and risk of obesity. Body mass index 16,876 European ancestry adult individuals 60,352 European ancestry adult individuals, 5,988 European ancestry children Affymetrix [344883] 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000185 Genome-wide genotyping array 2012-09-20 22823124 Verweij KJ 2012-07-24 Addict Biol www.ncbi.nlm.nih.gov/pubmed/22823124 The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation. Cannabis use (initiation) 10,091 individuals from 4,622 families NA Illumina [~ 2400000] (imputed) 6 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST001616 Genome-wide genotyping array 2012-03-23 22293537 Kiyotani K 2012-01-29 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/22293537 A genome-wide association study identifies four genetic markers for hematological toxicities in cancer patients receiving gemcitabine therapy. Response to gemcitabine in pancreatic cancer 21 Japanese ancestry adverse reaction cases, 58 Japanese ancestry non-adverse reaction individuals 33 Japanese ancestry adverse reaction cases, 62 Japanese ancestry non-adverse reaction individuals Illumina [470064] 2 response to gemcitabine http://purl.obolibrary.org/obo/GO_0036272 GCST001390 Genome-wide genotyping array 2011-05-11 21478494 Nan H 2011-04-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21478494 Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk. Cutaneous nevi 9,136 European ancestry individuals 3,581 European ancestry individuals Affymetrix, Illumina [2318094] (imputed) 3 nevus http://www.ebi.ac.uk/efo/EFO_0000625 GCST001034 Genome-wide genotyping array 2012-08-09 22701019 Sabater-Lleal M 2012-06-14 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/22701019 A genome-wide association study identifies KNG1 as a genetic determinant of plasma factor XI Level and activated partial thromboplastin time. Factor XI 339 European ancestry individuals from 21 families 658 European ancestry individuals Illumina [2543887] (imputed) 0 factor XI measurement http://www.ebi.ac.uk/efo/EFO_0004694 GCST001575 Genome-wide genotyping array 2012-12-21 23042114 Hirota T 2012-10-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23042114 Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population. Atopic dermatitis 1,472 Japanese ancestry cases, 7,971 Japanese ancestry controls 1,856 Japanese ancestry cases, 7,021 Japanese ancestry controls Illumina [606164] 17 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST001709 Genome-wide genotyping array 2012-07-17 22637743 Wei S 2012-05-27 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/22637743 Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility. Lung cancer (asbestos exposure interaction) 1,154 European ancestry cases, 1,137 European ancestry controls NA Illumina [307944] 2 lung carcinoma, asbestos exposure measurement http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0004806 GCST001543 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (cyclophosphamide) 168 Japanese ancestry cases, 335 Japanese ancestry controls NA Illumina [733202] 3 response to cyclophosphamide, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_1902518, http://purl.obolibrary.org/obo/GO_0097327 GCST002002 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (all antimicrotubule drugs) 371 Japanese ancestry cases, 825 Japanese ancestry controls NA Illumina [733202] 12 response to antineoplastic agent, response to antimicrotubule agent http://purl.obolibrary.org/obo/GO_0097327, http://www.ebi.ac.uk/efo/EFO_0005260 GCST002001 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (paclitaxel) 218 Japanese ancestry cases, 364 Japanese controls NA Illumina [733202] 8 methylcobalamin deficiency type cblE, response to antineoplastic agent http://purl.obolibrary.org/obo/MONDO_0009354, http://purl.obolibrary.org/obo/GO_0097327 GCST001999 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (docetaxel) 147 Japanese ancestry cases, 233 Japanese ancestry controls NA Illumina [733202] 7 response to docetaxel trihydrate, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_1902519, http://purl.obolibrary.org/obo/GO_0097327 GCST001995 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (all topoisomerase inhibitors) 106 Japanese ancestry cases, 187 Japanese ancestry controls NA Illumina [733202] 6 response to topoisomerase inhibitor, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0072758, http://purl.obolibrary.org/obo/GO_0097327 GCST001994 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (camptothecin) 59 Japanese ancestry cases, 155 Japanese ancestry controls NA Illumina [733202] 3 response to camptothecin, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_1901563, http://purl.obolibrary.org/obo/GO_0097327 GCST001993 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (etoposide) 54 Japanese ancestry cases, 39 Japanese ancestry controls NA Illumina [733202] 4 response to etoposide, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_1902521, http://purl.obolibrary.org/obo/GO_0097327 GCST002000 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (carboplatin) 261 Japanese ancestry cases, 262 Japanese ancestry controls NA Illumina [733202] 9 response to carboplatin, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097328, http://purl.obolibrary.org/obo/GO_0097327 GCST002004 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (all antimetabolite drugs) 294 Japanese ancestry cases, 2,249 Japanese ancestry controls NA Illumina [733202] 6 response to antineoplastic agent, response to antimetabolite http://purl.obolibrary.org/obo/GO_0097327, http://purl.obolibrary.org/obo/GO_0097329 GCST002005 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (paclitaxel + carboplatin) 150 Japanese ancestry cases, 166 Japanese ancestry controls NA Illumina [733202] 7 response to carboplatin, methylcobalamin deficiency type cblE, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097328, http://purl.obolibrary.org/obo/MONDO_0009354, http://purl.obolibrary.org/obo/GO_0097327 GCST002006 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (cisplatin) 176 Japanese ancestry cases, 471 Japanese ancestry controls NA Illumina [733202] 7 response to cisplatin, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0072718, http://purl.obolibrary.org/obo/GO_0097327 GCST002007 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (all anthracycline-based drugs) 184 Japanese ancestry cases, 459 Japanese ancestry controls NA Illumina [733202] 6 response to antineoplastic agent, response to anthracycline-based chemotherapy http://purl.obolibrary.org/obo/GO_0097327, http://www.ebi.ac.uk/efo/EFO_0005257 GCST002008 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (doxorubicin) 83 Japanese ancestry cases, 66 Japanese ancestry controls NA Illumina [733202] 3 response to antineoplastic agent, response to doxorubicin http://purl.obolibrary.org/obo/GO_0097327, http://purl.obolibrary.org/obo/GO_1902520 GCST002009 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (epirubicin) 83 Japanese ancestry cases, 370 Japanese ancestry controls NA Illumina [733202] 5 response to 4'-epidoxorubicin, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_1902522, http://purl.obolibrary.org/obo/GO_0097327 GCST001996 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (5-fluorouracil) 177 Japanese ancestry cases, 952 Japanese ancestry controls NA Illumina [733202] 4 response to 5-fluorouracil, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0036275, http://purl.obolibrary.org/obo/GO_0097327 GCST001997 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (all platinum-based drugs) 428 Japanese ancestry cases, 743 Japanese ancestry controls NA Illumina [733202] 6 response to platinum based chemotherapy, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0004647, http://purl.obolibrary.org/obo/GO_0097327 GCST001998 Genome-wide genotyping array 2013-11-14 23648065 Low SK 2013-05-04 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/23648065 Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan. Adverse response to chemotherapy (neutropenia/leucopenia) (gemcitabine) 80 Japanese ancestry cases, 226 Japanese ancestry controls NA Illumina [733202] 5 response to gemcitabine, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0036272, http://purl.obolibrary.org/obo/GO_0097327 GCST002003 Genome-wide genotyping array 2014-03-14 23982368 Qi L 2013-08-28 JAMA www.ncbi.nlm.nih.gov/pubmed/23982368 Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes. Cardiovascular heart disease in diabetics 669 European ancestry cases, 1,641 European ancestry controls 848 European ancestry cases, 1,030 European ancestry controls Affymetrix [2543016] 1 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST002153 Genome-wide genotyping array 2014-03-14 23983088 Miller FW 2013-08-27 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/23983088 Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders. Dermatomyositis 1,178 European ancestry cases, 4,724 European ancestry controls NA Illumina [up to 242876] 1 dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000398 GCST002151 Genome-wide genotyping array 2011-12-17 22101970 Kho AN 2011-11-19 J Am Med Inform Assoc www.ncbi.nlm.nih.gov/pubmed/22101970 Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study. Type 2 diabetes 2,413 European ancestry cases, 2,392 European ancestry controls, 810 African American cases, 873 African American controls NA Illumina [NR] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001326 Genome-wide genotyping array 2011-08-03 21725308 Hu Z 2011-07-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21725308 A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese. Lung cancer 2,331 Han Chinese ancestry cases, 3,077 Han Chinese ancestry controls 6,313 Han Chinese ancestry cases, 6,409 Han Chinese ancestry controls Affymetrix [906703] 4 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST001140 Genome-wide genotyping array 2013-09-12 23535733 Garcia-Closas M 2013-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23535733 Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Breast cancer 4,193 European ancestry cases, 35,194 European ancestry controls 6,514 European ancestry cases, 41,455 European ancestry controls Illumina [NR] 17 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001930 Genome-wide genotyping array 2012-04-20 22451204 Pankratz N 2012-03-01 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/22451204 Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Parkinson's disease 4,238 European ancestry cases, 4,239 European ancestry controls 3,738 European ancestry cases, 2,111 European ancestry controls Illumina [2500000] (imputed) 17 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST001430 Genome-wide genotyping array 2013-09-07 23562823 Sheu WH 2013-04-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23562823 Genome-wide association study in a Chinese population with diabetic retinopathy. Diabetic retinopathy 437 Chinese ancestry cases, 570 Chinese ancestry controls 329 Hispanic cases, 256 Hispanic controls Illumina [~ 2166765] (imputed) 1 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST001977 Genome-wide genotyping array 2011-07-14 21703634 Wang KS 2011-06-22 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/21703634 A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence. Alcohol dependence 1,283 European ancestry cases, 1,416 European ancestry controls 1,650 European ancestry cases and 1,684 European ancestry controls from 778 nuclear families Illumina [up to 818773] 2 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001121 Genome-wide genotyping array 2013-06-06 23362303 Wu JH 2013-01-29 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23362303 Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Palmitic acid (16:0) levels 8,961 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 12 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST001838 Genome-wide genotyping array 2013-06-06 23362303 Wu JH 2013-01-29 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23362303 Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Palmitoleic acid (16:1n-7) levels 8,961 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 15 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST001841 Genome-wide genotyping array 2013-06-06 23362303 Wu JH 2013-01-29 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23362303 Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Stearic acid (18:0) levels 8,961 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 11 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST001840 Genome-wide genotyping array 2013-06-05 23362303 Wu JH 2013-01-29 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23362303 Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Oleic acid (18:1n-9) levels 8,961 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 9 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST001834 Genome-wide genotyping array 2013-07-26 23512250 Xu H 2013-03-19 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/23512250 Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. Acute lymphoblastic leukemia (childhood) 972 European ancestry cases, 1,386 European ancestry controls, 89 African American cases, 1,363 African American controls, 305 Hispanic cases, 1,008 Hispanic controls 574 European ancestry cases, 2,601 European ancestry controls, 128 African American cases, 1,075 African American controls, 143 Hispanic cases, 640 Hispanic controls Affymetrix [709059] 3 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST001912 Genome-wide genotyping array 2009-04-14 19349984 Esparza-Gordillo J 2009-04-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19349984 A common variant on chromosome 11q13 is associated with atopic dermatitis. Atopic dermatitis 939 European ancestry cases, 975 European ancestry controls, 1,097 European ancestry individuals from 270 families 2,637 European ancestry cases, 3,957 European ancestry controls Affymetrix [342303] 1 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST000374 Genome-wide genotyping array 2013-05-26 23454411 Lin MT 2013-02-27 Transl Res www.ncbi.nlm.nih.gov/pubmed/23454411 A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease. Coronary arterial lesions in patients with Kawasaki disease 64 East Asian ancestry serious cases, 70 East Asian ancestry minor cases 117 East Asian ancestry serious cases, 128 East Asian ancestry minor cases Affymetrix [470949] 0 coronary aneurysm http://www.ebi.ac.uk/efo/EFO_1000881 GCST001878 Genome-wide genotyping array 2012-05-11 22457343 Martinelli-Boneschi F 2012-03-28 Mult Scler www.ncbi.nlm.nih.gov/pubmed/22457343 A genome-wide association study in progressive multiple sclerosis. Multiple sclerosis 197 European ancestry cases, 234 European ancestry controls 379 European ancestry cases, 398 European ancestry controls Affymetrix [277866] 1 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST001459 Genome-wide genotyping array 2012-04-27 22424883 Imboden M 2012-03-15 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/22424883 Genome-wide association study of lung function decline in adults with and without asthma. Pulmonary function decline 1,441 European ancestry asthma cases, 2,677 European ancestry controls 1,160 European ancestry asthma cases, 10,858 European ancestry controls Illumina [~ 2500000] (imputed) 39 forced expiratory volume, FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0004713 GCST001444 Genome-wide genotyping array 2012-12-04 23021708 Kerns SL 2012-09-26 Int J Radiat Oncol Biol Phys www.ncbi.nlm.nih.gov/pubmed/23021708 A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of erectile dysfunction following radiation therapy for prostate cancer. Erectile dysfunction and prostate cancer treatment 132 African American, European, Hispanic/Latin American, East Asian and South Asian ancestry cases, 103 African American, European, Hispanic/Latin American, East Asian ancestry and South Asian ancestry controls 128 African American, European, Hispanic/Latin American, East Asian and South Asian ancestry cases, 102 African American, European, Hispanic/Latin American, East Asian and South Asian ancestry controls Affymetrix [614453] 0 response to radiation, prostate carcinoma, erectile dysfunction http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0001663, http://www.ebi.ac.uk/efo/EFO_0004234 GCST001700 Genome-wide genotyping array 2014-02-25 23894154 Kohler A 2013-07-26 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/23894154 Genome-wide association study on differentiated thyroid cancer. Thyroid cancer 690 European ancestry cases, 497 European ancestry controls 2,958 European ancestry cases, 3,727 European ancestry controls Illumina [572042] 2 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST002102 Genome-wide genotyping array 2012-05-25 22503698 Bhatnagar R 2012-04-12 Oral Oncol www.ncbi.nlm.nih.gov/pubmed/22503698 Genome-wide disease association study in chewing tobacco associated oral cancers. Oral cancers (chewing tobacco related) 55 South Asian ancestry cases, 92 South Asian ancestry controls NA Illumina [316018] 0 matrix metalloproteinase measurement, mouth neoplasm http://www.ebi.ac.uk/efo/EFO_0004744, http://www.ebi.ac.uk/efo/EFO_0003868 GCST001480 Genome-wide genotyping array 2012-04-20 22445761 Kurose K 2012-03-23 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/22445761 Genome-wide association study of SSRI/SNRI-induced sexual dysfunction in a Japanese cohort with major depression. Sexual dysfunction (SSRI/SNRI-related) 201 Japanese ancestry individuals NA Affymetrix [186320] 5 sexual dysfunction http://www.ebi.ac.uk/efo/EFO_0004714 GCST001453 Genome-wide genotyping array 2012-07-26 22694930 Li X 2012-06-11 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/22694930 Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases. Asthma 813 European ancestry cases, 1,011 European ancestry controls TENOR and GABRIEL studies Illumina [474271] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001564 Genome-wide genotyping array 2015-05-06 23575227 Urbanek M 2013-04-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23575227 The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study. Anthropometric traits in newborns 1,095 Afro-Caribbean individuals, 1,363 European ancestry individuals, 616 Mexican American individuals, 1,207 Thai ancestry individuals 2,296 European ancestry individuals Illumina [up to 3563305] (imputed) 5 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST001964 Genome-wide genotyping array 2013-05-16 23423446 Hein R 2013-02-20 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/23423446 A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication. Breast cancer (menopausal hormone therapy interaction) 731 European ancestry cases 7,965 European and East Asian ancestry cases, 8,128 European and East Asian ancestry controls Illumina [316974] 0 breast carcinoma, hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0003961 GCST001869 Genome-wide genotyping array 2012-04-18 22446040 Wang KS 2012-03-16 Gene www.ncbi.nlm.nih.gov/pubmed/22446040 A novel locus for body mass index on 5p15.2: a meta-analysis of two genome-wide association studies. Body mass index 5,218 European ancestry individuals 762 European ancestry individuals Illumina [up to 520531] 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001448 Genome-wide genotyping array 2012-08-17 22589738 Fox CS 2012-05-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22589738 Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. Subcutaneous adipose tissue 5,560 European ancestry female individuals, 4,997 European ancestry male individuals NA Affymetrix, Illumina [2500000] (imputed) 39 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST001521 Genome-wide genotyping array 2012-08-17 22589738 Fox CS 2012-05-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22589738 Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. Visceral fat 5,560 European ancestry female individuals, 4,997 European ancestry male individuals NA Affymetrix, Illumina [2500000] (imputed) 40 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST001525 Genome-wide genotyping array 2012-08-17 22589738 Fox CS 2012-05-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22589738 Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. Visceral adipose tissue/subcutaneous adipose tissue ratio 5,560 European ancestry female individuals, 4,997 European ancestry male individuals NA Affymetrix, Illumina [2500000] (imputed) 42 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST001524 Genome-wide genotyping array 2012-08-17 22589738 Fox CS 2012-05-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22589738 Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. Visceral adipose tissue adjusted for BMI 5,560 European ancestry female individuals, 4,997 European ancestry male individuals NA Affymetrix, Illumina [2500000] (imputed) 45 visceral adipose tissue measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004765, http://www.ebi.ac.uk/efo/EFO_0004340 GCST001523 Genome-wide genotyping array 2012-08-15 22693459 Li R 2012-05-31 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22693459 Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases. Male-pattern baldness 3,891 European ancestry cases, 8,915 European ancestry controls NA Affymetrix, Illumina [2391230] (imputed) 8 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST001548 Genome-wide genotyping array 2010-09-14 20675712 Reed DR 2010-07-31 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20675712 The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12. Bitter taste response 1,457 European ancestry individuals 73 European ancestry individuals Illumina [~ 2300000] (imputed) 1 sensory perception of bitter taste http://purl.obolibrary.org/obo/GO_0050913 GCST000746 Genome-wide genotyping array 2012-03-13 22333899 Wei WH 2012-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22333899 Genome-wide analysis of epistasis in body mass index using multiple human populations. Body mass index (SNP x SNP interaction) 3,653 European ancestry individuals 5,071 European ancestry individuals Illumina [NR] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001409 Genome-wide genotyping array 2013-09-27 23551011 Zhao L 2013-04-02 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23551011 Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. Preeclampsia 21 Afro-Caribbean cases, 1,010 Afro-Caribbean controls, 50 European ancestry cases, 1,202 European ancestry controls, 62 Hispanic cases, 658 Hispanic controls NA Illumina [2485249] (imputed) 18 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST001949 Genome-wide genotyping array 2012-05-23 22466613 Sun L 2012-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22466613 Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis. Cystic fibrosis (meconium ileus) 3,763 European ancestry cases 2,372 European ancestry cases Illumina [7245292] (imputed) 0 cystic fibrosis associated meconium ileus http://www.ebi.ac.uk/efo/EFO_0004608 GCST001468 Genome-wide genotyping array 2011-09-08 21829389 Barbalic M 2011-08-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829389 Genome-wide association analysis of incident coronary heart disease (CHD) in African Americans: a short report. Coronary heart disease 362 African American cases, 2,543 African American controls 862 African American female cases, 7,293 African American female controls Affymetrix [NR] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001190 Genome-wide genotyping array 2008-06-16 18326623 Gold B 2008-03-11 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/18326623 Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. Breast cancer 249 Ashkenazi Jewish non-BRCA1/2 carriers cases, 299 Ashkenazi Jewish non-BRCA1/2 carriers controls 1,193 Ashkenazi Jewish non-BRCA1/2 carriers cases,1,166 Ashkenazi Jewish non-BRCA1/2 carriers controls Affymetrix [150080] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000162 Genome-wide genotyping array 2013-02-21 23267103 Desch KC 2012-12-24 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/23267103 Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association. Coagulation factor levels 3,250 European ancestry individuals, up to 212 individuals NA Illumina [723716] 7 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST001793 Genome-wide genotyping array 2012-09-18 22792221 Takamoto M 2012-07-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/22792221 Common variants on chromosome 9p21 are associated with normal tension glaucoma. Glaucoma 286 Japanese ancestry cases, 557 Japanese ancestry controls 334 Japanese ancestry cases, 701 Japanese ancestry controls Affymetrix [531009] 1 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST001596 Genome-wide genotyping array 2012-12-11 22960999 Wu C 2012-09-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22960999 Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions. Esophageal cancer (squamous cell) 2,031 Han Chinese ancestry cases, 2,044 Han Chinese ancestry controls 8,092 Chinese ancestry cases, 8,620 Chinese ancestry controls NR [NR] 7 squamous cell carcinoma, esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0000707, http://www.ebi.ac.uk/efo/EFO_0002916 GCST001674 Genome-wide genotyping array 2012-12-11 22960999 Wu C 2012-09-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22960999 Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions. Esophageal cancer (alcohol interaction) 2,031 Han Chinese ancestry cases, 2,044 Han Chinese ancestry controls 8,092 Chinese ancestry cases, 8,620 Chinese ancestry controls NR [NR] 4 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST001672 Genome-wide genotyping array 2011-01-10 21105107 Clifford RJ 2010-12-01 Hepatology www.ncbi.nlm.nih.gov/pubmed/21105107 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. Hepatocellular carcinoma 180 Korean ancestry cases, 271 Korean ancestry controls 206 Korean ancestry cases, 416 East Asian ancestry controls, Affymetrix [658897] 3 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST000902 Genome-wide genotyping array 2011-01-11 21124317 Wang K 2010-12-01 Nature www.ncbi.nlm.nih.gov/pubmed/21124317 Integrative genomics identifies LMO1 as a neuroblastoma oncogene. Neuroblastoma 1,627 European ancestry child cases, 3,254 European ancestry child controls 624 European ancestry child cases, 2,843 European ancestry child controls Illumina [480279] 3 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST000901 Genome-wide genotyping array 2009-06-21 19458352 Hirschfield GM 2009-05-20 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants. Primary biliary cholangitis 505 European ancestry cases, 1,507 European ancestry controls 526 European ancestry cases, 1,206 European ancestry controls Illumina [305724] 7 biliary liver cirrhosis http://www.ebi.ac.uk/efo/EFO_0004267 GCST000408 Genome-wide genotyping array 2012-03-30 22365631 Greenwood TA 2012-02-22 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22365631 Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci. Temperament (bipolar disorder) 1,263 European ancestry cases, 1,434 European ancestry controls NA Affymetrix [703012] 13 behavior or behavioral disorder measurement, personality trait http://www.ebi.ac.uk/efo/EFO_0004782, http://www.ebi.ac.uk/efo/EFO_0004365 GCST001419 Genome-wide genotyping array 2009-12-29 20031576 Dehghan A 2009-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031576 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. Fibrinogen 22,096 European ancestry individuals 17,686 European ancestry female individuals Affymetrix, Illumina [~ 2661766] (imputed) 4 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST000366 Genome-wide genotyping array 2010-06-14 20463881 Liu F 2010-05-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20463881 Digital quantification of human eye color highlights genetic association of three new loci. Eye color traits 5,951 European ancestry individuals 3,543 European ancestry individuals Illumina [2543887] (imputed) 3 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST000685 Genome-wide genotyping array 2011-04-13 21396408 Miller EK 2011-03-25 Vaccine www.ncbi.nlm.nih.gov/pubmed/21396408 Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age. Vaccine-related adverse events 6 European ancestry cases,55 European ancestry controls NA Illumina [468458] 2 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST001016 Genome-wide genotyping array 2008-09-16 18193043 Willer CJ 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193043 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. HDL cholesterol 8,656 European ancestry individuals 11,437 European ancestry individuals Affymetrix, Illumina [~ 2261000] (imputed) 10 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000135 Genome-wide genotyping array 2008-09-16 18193043 Willer CJ 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193043 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. LDL cholesterol 8,589 European ancestry individuals 12,981 European ancestry individuals Affymetrix, Illumina [~ 2261000] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000132 Genome-wide genotyping array 2008-09-16 18193043 Willer CJ 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193043 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. Triglycerides 8,684 European ancestry individuals 9,741 European ancestry individuals Affymetrix, Illumina [~ 2261000] (imputed) 9 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000139 Genome-wide genotyping array 2009-02-16 17952075 Sulem P 2007-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17952075 Genetic determinants of hair, eye and skin pigmentation in Europeans. Skin sensitivity to sun 2,986 Icelandic ancestry individuals 3,932 European ancestry individuals Illumina [317511] 2 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST000116 Genome-wide genotyping array 2009-02-16 17952075 Sulem P 2007-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17952075 Genetic determinants of hair, eye and skin pigmentation in Europeans. Red vs non-red hair color 2,986 Icelandic ancestry individuals 3,932 European ancestry individuals Illumina [317511] 1 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST000115 Genome-wide genotyping array 2008-06-16 17952075 Sulem P 2007-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17952075 Genetic determinants of hair, eye and skin pigmentation in Europeans. Freckles 2,986 Icelandic ancestry individuals 3,932 European ancestry individuals Illumina [317511] 3 freckles http://www.ebi.ac.uk/efo/EFO_0003963 GCST000119 Genome-wide genotyping array 2008-06-16 17952075 Sulem P 2007-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17952075 Genetic determinants of hair, eye and skin pigmentation in Europeans. Blond vs. brown hair color 2,986 Icelandic ancestry individuals 3,932 European ancestry individuals Illumina [317511] 4 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST000118 Genome-wide genotyping array 2008-06-16 17952075 Sulem P 2007-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17952075 Genetic determinants of hair, eye and skin pigmentation in Europeans. Blue vs. green eyes 2,986 Icelandic ancestry individuals 3,932 European ancestry individuals Illumina [317511] 3 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST000117 Genome-wide genotyping array 2009-02-16 17952075 Sulem P 2007-10-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17952075 Genetic determinants of hair, eye and skin pigmentation in Europeans. Blue vs. brown eyes 2,986 Icelandic ancestry individuals 3,932 European ancestry individuals Illumina [317511] 1 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST000120 Genome-wide genotyping array 2009-09-29 19734901 van Es MA 2009-09-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19734901 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 2,323 European ancestry cases, 9,013 European ancestry controls 2,532 European ancestry cases, 5,940 European ancestry controls Illumina [292768] 8 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000481 Genome-wide genotyping array 2010-07-04 20534544 Beall CM 2010-06-22 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/20534544 Natural selection on EPAS1 (HIF2alpha) associated with low hemoglobin concentration in Tibetan highlanders. Hemoglobin levels 35 Tibetan ancestry individuals 161 Tibetan ancestry individuals Illumina [502722] 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST000704 Genome-wide genotyping array 2011-03-02 21244703 Wang JH 2011-01-18 Genome Med www.ncbi.nlm.nih.gov/pubmed/21244703 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. Multiple sclerosis 2,124 cases, 6,720 controls 1,618 cases, 1,988 controls Affymetrix, Illumina [~ 2560000] (imputed) 3 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000949 Genome-wide genotyping array 2013-03-28 23291589 Lu Y 2013-01-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23291589 Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus. Corneal structure 13,057 European ancestry individuals, 2,538 Indian ancestry individuals, 2,542 Malay ancestry individuals, 1,883 Chinese ancestry individuals NA Affymetrix, Illumina [~ 1000000] (imputed) 26 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST001806 Genome-wide genotyping array 2011-04-06 21390209 Hu X 2011-02-24 PLoS One www.ncbi.nlm.nih.gov/pubmed/21390209 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. Alzheimer's disease (late onset) 1,831 European ancestry cases, 1,764 European ancestry controls 751 cases, 751 controls Affymetrix, Illumina [NR] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000986 Genome-wide genotyping array 2010-07-12 20543847 Turnbull C 2010-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20543847 Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer. Testicular germ cell cancer 979 European ancestry cases, 4,947 European ancestry controls 664 European ancestry cases, 3,456 European ancestry controls Illumina [298782] 6 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST000701 Genome-wide genotyping array 2008-09-16 18239089 Kong A 2008-02-02 Science www.ncbi.nlm.nih.gov/pubmed/18239089 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. Recombination rate (males) 1,887 male individuals 1,248 male individuals Illumina [309241] 1 recombination rate http://www.ebi.ac.uk/efo/EFO_0004863 GCST000148 Genome-wide genotyping array 2008-09-17 18239089 Kong A 2008-02-02 Science www.ncbi.nlm.nih.gov/pubmed/18239089 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. Recombination rate (females) 1,702 female individuals 1,663 female individuals Illumina [309241] 1 recombination rate http://www.ebi.ac.uk/efo/EFO_0004863 GCST000149 Genome-wide genotyping array 2011-04-11 21386085 Kraja AT 2011-03-08 Diabetes www.ncbi.nlm.nih.gov/pubmed/21386085 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Metabolic syndrome (bivariate traits) 22,161 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 16 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST001007 Genome-wide genotyping array 2011-04-11 21386085 Kraja AT 2011-03-08 Diabetes www.ncbi.nlm.nih.gov/pubmed/21386085 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Metabolic syndrome 22,161 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 5 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST001003 Genome-wide genotyping array 2011-04-11 21386085 Kraja AT 2011-03-08 Diabetes www.ncbi.nlm.nih.gov/pubmed/21386085 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Waist Circumference - Triglycerides (WC-TG) 22,161 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 7 triglyceride measurement, metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0000195 GCST001006 Genome-wide genotyping array 2011-04-11 21386085 Kraja AT 2011-03-08 Diabetes www.ncbi.nlm.nih.gov/pubmed/21386085 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. HDL Cholesterol - Triglycerides (HDLC-TG) 22,161 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST001005 Genome-wide genotyping array 2011-04-11 21386085 Kraja AT 2011-03-08 Diabetes www.ncbi.nlm.nih.gov/pubmed/21386085 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. Triglycerides-Blood Pressure (TG-BP) 22,161 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 6 triglyceride measurement, blood pressure http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004325 GCST001004 Genome-wide genotyping array 2010-06-02 20451256 Djurovic S 2010-05-05 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/20451256 A genome-wide association study of bipolar disorder in Norwegian individuals, followed by replication in Icelandic sample. Bipolar disorder 194 European ancestry bipolar cases, 230 European ancestry schizophrenic cases, 336 European ancestry controls 435 European ancestry bipolar cases, 10,258 European ancestry controls Affymetrix [up to 620390] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000674 Genome-wide genotyping array 2008-06-16 17618284 Tomlinson I 2007-07-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17618284 A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. Colorectal cancer 930 European ancestry cases, 960 European ancestry controls 7,334 European ancestry cases, 5,246 European ancestry controls Illumina [547647] 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000053 Genome-wide genotyping array 2011-04-06 21355061 Boger CA 2011-02-25 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/21355061 CUBN is a gene locus for albuminuria. Urinary albumin excretion 31,580 European ancestry individuals 31,277 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 1 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST000988 Genome-wide genotyping array 2008-09-12 17903300 Fox CS 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903300 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. Waist circumference 1,079 European ancestry individuals from 310 families NA Affymetrix [70897] 2 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST000084 Genome-wide genotyping array 2008-09-17 17903300 Fox CS 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903300 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. Body mass index 1,341 European ancestry individuals from 310 families NA Affymetrix [70897] 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000090 Genome-wide genotyping array 2013-04-19 23326517 Holliday EG 2013-01-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/23326517 Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis. Age-related macular degeneration 3,772 European ancestry cases, 16,033 European ancestry controls 264 Asian ancestry cases, 3,926 Asian ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 31 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST001814 Genome-wide genotyping array 2011-04-07 21408207 Chung SA 2011-03-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21408207 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. Systemic lupus erythematosus 811 anti-dsDNA positive European ancestry cases, 906 anti-dsDNA negative European ancestry cases, 4,813 European ancestry controls NA Illumina [421318] (imputed) 24 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000996 Genome-wide genotyping array 2012-02-21 22291604 Okada Y 2012-01-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22291604 A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese. Systemic lupus erythematosus 891 Japanese ancestry cases, 3,384 Japanese ancestry controls 1,387 Japanese ancestry cases, 28,564 Japanese ancestry controls Illumina [430797] 2 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST001384 Genome-wide genotyping array 2011-06-01 21540310 Hofmann S 2011-05-03 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/21540310 A genome-wide association study reveals evidence of association with sarcoidosis at 6p12.1. Sarcoidosis 381 European ancestry cases, 392 European ancestry controls 1,582 European ancestry cases, 1,783 European ancestry controls Affymetrix [97088] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST001064 Genome-wide genotyping array 2009-03-28 19259986 Hattori E 2009-03-02 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/19259986 Preliminary genome-wide association study of bipolar disorder in the Japanese population. Bipolar disorder 107 Japanese ancestry cases, 107 Japanese ancestry controls 395 Japanese ancestry cases, 409 Japanese ancestry controls Affymetrix [88671] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000350 Genome-wide genotyping array 2011-04-04 21326295 Jin Y 2011-02-17 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/21326295 Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset. Vitiligo 1,339 European ancestry cases 677 European ancestry cases Illumina [520460] 1 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST000981 Genome-wide genotyping array 2013-09-27 20197096 Stein JL 2010-03-01 Neuroimage www.ncbi.nlm.nih.gov/pubmed/20197096 Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Brain structure (hippocampal volume) 162 European ancestry Alzheimer's disease cases, 343 European ancestry amnestic mild cognitive impairment cases, 193 European ancestry healthy elderly controls NA Illumina [546314] 4 brain measurement, hippocampal volume http://www.ebi.ac.uk/efo/EFO_0004464, http://www.ebi.ac.uk/efo/EFO_0005035 GCST000615 Genome-wide genotyping array 2013-09-27 20197096 Stein JL 2010-03-01 Neuroimage www.ncbi.nlm.nih.gov/pubmed/20197096 Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease. Brain structure (temporal lobe volume) 173 European ancestry Alzheimer's disease cases, 361 European ancestry Mild Cognitive Impairment cases, 208 European ancestry controls NA Illumina [546314] 5 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000614 Genome-wide genotyping array 2011-04-11 21423719 Speliotes EK 2011-03-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21423719 Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. Nonalcoholic fatty liver disease 880 Amish individuals, 6,296 European ancestry individuals 592 European ancestry cases, 1,405 European ancestry controls Affymetrix, Illumina [~ 2400000] (imputed) 1 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST001008 Genome-wide genotyping array 2008-06-16 18179892 Wallace C 2008-01-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18179892 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. LDL cholesterol 1,955 European ancestry hypertensive individuals 2,033 European ancestry individuals from 519 families, 1,461 European ancestry twins Affymetrix [400496] 3 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000131 Genome-wide genotyping array 2008-06-16 18179892 Wallace C 2008-01-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18179892 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. Urate levels 1,955 European ancestry hypertensive individuals 2,033 European ancestry individuals from 519 families, 1,461 European ancestry twins Affymetrix [400496] 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST000130 Genome-wide genotyping array 2008-06-16 17505501 Kindmark A 2007-05-15 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/17505501 Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis. Response to ximelagatran treatment (increased serum alanine aminotransferase levels) 74 European ancestry cases, 130 European ancestry treated controls 10 European ancestry cases, 16 European ancestry treated controls Perlegen [~ 266722] 0 serum alanine aminotransferase measurement, response to ximelagatran http://www.ebi.ac.uk/efo/EFO_0004735, http://purl.obolibrary.org/obo/GO_0036288 GCST000034 Genome-wide genotyping array 2010-01-13 20037589 Illig T 2009-12-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20037589 A genome-wide perspective of genetic variation in human metabolism. Metabolite levels 1,029 European ancestry individuals 1,202 European ancestry individuals Affymetrix [517480] 5 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST000550 Genome-wide genotyping array 2008-12-11 19043545 Gieger C 2008-11-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19043545 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. Metabolite levels 284 European ancestry male individuals NA Affymetrix [187454] 16 phenylalanine measurement, acylcarnitine measurement, carbohydrate measurement, tyrosine measurement, sphingolipid measurement, lysine measurement, lipid measurement, phospholipid measurement, serotonin measurement http://www.ebi.ac.uk/efo/EFO_0005001, http://www.ebi.ac.uk/efo/EFO_0005059, http://www.ebi.ac.uk/efo/EFO_0004998, http://www.ebi.ac.uk/efo/EFO_0005058, http://www.ebi.ac.uk/efo/EFO_0004622, http://www.ebi.ac.uk/efo/EFO_0005002, http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004846 GCST000274 Genome-wide genotyping array 2008-11-12 18849991 Richards JB 2008-10-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18849991 Male-pattern baldness susceptibility locus at 20p11. Male-pattern baldness 578 European ancestry cases, 547 European ancestry controls 1,351 European ancestry cases, 2,485 European ancestry controls Affymetrix [370102] 2 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST000250 Genome-wide genotyping array 2012-02-02 22233651 Kwak SH 2012-01-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/22233651 A genome-wide association study of gestational diabetes mellitus in Korean women. Diabetes (gestational) 468 Korean ancestry cases, 1,242 Korean ancestry controls 931 Korean ancestry cases, 783 Korean ancestry controls Affymetrix [2188613] (imputed) 3 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST001375 Genome-wide genotyping array 2008-09-15 18262040 Sandhu MS 2008-02-09 Lancet www.ncbi.nlm.nih.gov/pubmed/18262040 LDL-cholesterol concentrations: a genome-wide association study. LDL cholesterol 11,685 European ancestry individuals Up to 4,979 European ancestry individuals Affymetrix, Illumina [up to 461986] 3 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000151 Genome-wide genotyping array 2009-12-29 19767753 Eeles RA 2009-09-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19767753 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. Prostate cancer 1,854 European ancestry cases, 1,894 European ancestry controls 19,879 cases and 18,761 controls of European, East Asian, African American, Latino, and Hawaiian ancestry Illumina [541129] 19 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000488 Genome-wide genotyping array 2008-09-10 17903298 Meigs JB 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903298 Genome-wide association with diabetes-related traits in the Framingham Heart Study. Fasting plasma glucose 1,027 individuals NA Affymetrix [70897] 6 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000085 Genome-wide genotyping array 2009-09-15 17903298 Meigs JB 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903298 Genome-wide association with diabetes-related traits in the Framingham Heart Study. Diabetes (incident) 91 cases, 1,083 controls NA Affymetrix [70897] 1 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST000108 Genome-wide genotyping array 2008-09-10 17903298 Meigs JB 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903298 Genome-wide association with diabetes-related traits in the Framingham Heart Study. Diabetes related insulin traits Up to 982 individuals NA Affymetrix [70897] 4 insulin sensitivity measurement, HbA1c measurement, insulin resistance, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0004541, http://www.ebi.ac.uk/efo/EFO_0002614, http://www.ebi.ac.uk/efo/EFO_0004466 GCST000077 Genome-wide genotyping array 2013-09-28 23665963 Dubinsky MC 2013-05-09 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/23665963 Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease. Crohn's disease (time to surgery) 983 European ancestry cases NA Illumina [484724] 1 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST002018 Genome-wide genotyping array 2013-09-28 23665963 Dubinsky MC 2013-05-09 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/23665963 Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease. Crohn's disease (need for surgery) 239 European ancestry cases that required surgery within 5 year, 375 European ancestry cases that did not require surgery within 5 years NA Illumina [483359] 2 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST002017 Genome-wide genotyping array 2009-09-28 17848626 Florez JC 2007-09-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/17848626 A 100K genome-wide association scan for diabetes and related traits in the Framingham Heart Study: replication and integration with other genome-wide datasets. Type 2 diabetes and 6 quantitative traits 1,087 European ancestry individuals from 307 families 1,465 European ancestry individuals, 1,464 European ancestry cases, 1,467 European ancestry controls, 300 Pima Indian ancestry cases, 334 Pima Indian ancestry controls, 287 Mexican American cases, 316 Mexican American controls, 124 Old Order Amish cases, 295 Old Order Amish controls Affymetrix [66543] 0 insulin measurement, glucose measurement, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0004467, http://www.ebi.ac.uk/efo/EFO_0004468, http://purl.obolibrary.org/obo/MONDO_0005148 GCST000073 Genome-wide genotyping array 2010-10-07 20877124 Hiura Y 2010-09-18 Circ J www.ncbi.nlm.nih.gov/pubmed/20877124 A genome-wide association study of hypertension-related phenotypes in a Japanese population. Hypertension 936 Japanese ancestry individuals 6,123 Japanese ancestry individuals Illumina [368274] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST000799 Genome-wide genotyping array 2008-06-16 17667963 Shifman S 2007-07-31 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/17667963 A whole genome association study of neuroticism using DNA pooling. Neuroticism 1,038 European ancestry cases, 1,016 European ancestry controls 831 European ancestry cases, 702 European ancestry controls Affymetrix [452574] 1 neurotic disorder http://www.ebi.ac.uk/efo/EFO_0004257 GCST000063 Genome-wide genotyping array 2009-11-03 19862010 Ganesh SK 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19862010 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Mean corpuscular hemoglobin 24,167 European ancestry individuals 9,456 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 9 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST000504 Genome-wide genotyping array 2009-11-03 19862010 Ganesh SK 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19862010 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Hematocrit 24,167 European ancestry individuals 9,456 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 8 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST000502 Genome-wide genotyping array 2009-11-03 19862010 Ganesh SK 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19862010 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Mean corpuscular volume 24,167 European ancestry individuals 9,456 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 17 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST000503 Genome-wide genotyping array 2009-11-03 19862010 Ganesh SK 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19862010 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Hemoglobin 24,167 European ancestry individuals 9,456 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 7 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST000499 Genome-wide genotyping array 2009-11-03 19862010 Ganesh SK 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19862010 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. Other erythrocyte phenotypes 24,167 European ancestry individuals 9,456 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 4 erythrocyte count, mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528 GCST000500 Genome-wide genotyping array 2008-09-11 17903293 Benjamin EJ 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903293 Genome-wide association with select biomarker traits in the Framingham Heart Study. Select biomarker traits 1,012 European ancestry individuals NA Affymetrix [70897] 21 vitamin K measurement, alkaline phosphatase measurement, CD40 ligand measurement, tumor necrosis factor-alpha measurement, serum alanine aminotransferase measurement, atrial natriuretic factor measurement, C-reactive protein measurement, CCL2 measurement, bilirubin measurement, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004618, http://www.ebi.ac.uk/efo/EFO_0004533, http://www.ebi.ac.uk/efo/EFO_0004790, http://www.ebi.ac.uk/efo/EFO_0004684, http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0004789, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0004749, http://www.ebi.ac.uk/efo/EFO_0004570, http://www.ebi.ac.uk/efo/EFO_0004631 GCST000083 Genome-wide genotyping array 2008-09-12 18245381 Uda M 2008-02-05 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/18245381 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. Fetal hemoglobin levels 4,305 European ancestry individuals 521 European ancestry individuals Affymetrix [362129] 2 fetal hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004576 GCST000150 Genome-wide genotyping array 2011-02-25 21242121 Frullanti E 2011-01-17 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/21242121 Multiple genetic loci modulate lung adenocarcinoma clinical staging. Lung adenocarcinoma (clinical stage) 600 European ancestry cases 317 European ancestry cases Illumina [620901] 0 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST000947 Genome-wide genotyping array 2010-12-01 20971583 Ojwang JO 2010-10-22 J Hand Surg Am www.ncbi.nlm.nih.gov/pubmed/20971583 Genome-wide association scan of Dupuytren's disease. Dupuytren's disease 37 European ancestry cases, 36 European ancestry controls NA Illumina [251837] 1 Dupuytren Contracture http://www.ebi.ac.uk/efo/EFO_0004229 GCST000841 Genome-wide genotyping array 2009-09-28 17998437 Li H 2007-11-12 Arch Neurol www.ncbi.nlm.nih.gov/pubmed/17998437 Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. Alzheimer's disease 753 European ancestry cases, 736 European ancestry controls 418 European ancestry cases, 249 European ancestry controls Affymetrix [469438] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000124 Genome-wide genotyping array 2012-01-19 22197933 Hu Z 2011-12-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22197933 A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia. Non-obstructive azoospermia 981 Han Chinese ancestry cases, 1,657 Han Chinese ancestry controls 1,946 Han Chinese ancestry cases, 4,077 Han Chinese ancestry controls Affymetrix [587347] 4 azoospermia http://www.ebi.ac.uk/efo/EFO_0000279 GCST001362 Genome-wide genotyping array 2009-09-28 17767157 Weedon MN 2007-09-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17767157 A common variant of HMGA2 is associated with adult and childhood height in the general population. Height 4,921 European ancestry individuals 19,064 European ancestry adult individuals, 6,827 European ancestry children Affymetrix [364301] 1 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000068 Genome-wide genotyping array 2013-11-29 23732972 Hashimoto R 2013-06-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/23732972 Genome-wide association study of cognitive decline in schizophrenia. Cognitive decline 166 Japanese ancestry schizophrenia cases, 323 Japanese ancestry controls 339 schizophrenia cases Affymetrix [541657] 0 Mental deterioration http://purl.obolibrary.org/obo/HP_0001268 GCST002055 Genome-wide genotyping array 2009-03-29 19282985 Liu YZ 2009-03-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19282985 Genome-wide association analyses identify SPOCK as a key novel gene underlying age at menarche. Menarche (age at onset) 477 European ancestry females 854 European ancestry siblings, 762 European ancestry female individuals, 1,387 Chinese ancestry female individuals Affymetrix [379319] 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST000355 Genome-wide genotyping array 2008-06-16 17558408 van Heel DA 2007-06-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17558408 A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. Celiac disease 778 European ancestry cases, 1,422 European ancestry controls 991 European ancestry cases, 1,489 European ancestry controls Illumina [310605] 2 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST000048 Genome-wide genotyping array 2008-06-16 15761122 Klein RJ 2005-03-10 Science www.ncbi.nlm.nih.gov/pubmed/15761122 Complement factor H polymorphism in age-related macular degeneration. Age-related macular degeneration 96 European ancestry cases, 50 European ancestry controls NA Affymetrix [103611] 1 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST000001 Genome-wide genotyping array 2008-06-16 17434096 Matarin M 2007-05-06 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/17434096 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. Stroke 249 European ancestry cases, 268 European ancestry controls NA Illumina [408803] 4 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST000032 Genome-wide genotyping array 2008-06-16 18193044 Kathiresan S 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193044 Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. Triglycerides 2,758 European ancestry individuals 18,554 European ancestry individuals Affymetrix [389878] 9 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000138 Genome-wide genotyping array 2008-06-16 18193044 Kathiresan S 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193044 Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. LDL cholesterol 2,758 European ancestry individuals 18,544 European ancestry individuals Affymetrix [389878] 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000134 Genome-wide genotyping array 2008-06-16 18193044 Kathiresan S 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193044 Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. HDL cholesterol 2,758 European ancestry individuals 18,554 European ancestry individuals Affymetrix [389878] 6 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000133 Genome-wide genotyping array 2010-01-19 20038948 Papassotiropoulos A 2009-12-29 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20038948 A genome-wide survey of human short-term memory. Memory (short-term) 333 European ancestry individuals 777 European ancestry young individuals, 922 European ancestry elderly individuals Affymetrix [841663] 0 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST000552 Genome-wide genotyping array 2008-08-28 17903294 Yang Q 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903294 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. Factor VII 886 European ancestry individuals NA Affymetrix [70897] 4 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST000082 Genome-wide genotyping array 2008-08-28 17903294 Yang Q 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903294 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. Hemostatic factors and hematological phenotypes Up to 1,062 European ancestry individuals NA Affymetrix [70897] 18 platelet aggregation, hemoglobin measurement, erythrocyte count, mean corpuscular hemoglobin, blood viscosity, tissue plasminogen activator measurement, plasminogen activator inhibitor 1 measurement http://purl.obolibrary.org/obo/GO_0070527, http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004527, http://www.ebi.ac.uk/efo/EFO_0004301, http://www.ebi.ac.uk/efo/EFO_0004791, http://www.ebi.ac.uk/efo/EFO_0004792 GCST000080 Genome-wide genotyping array 2015-05-12 22013104 Melka MG 2011-10-19 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/22013104 Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure. Obesity-related traits 598 French Canadian founder adolescent individuals NA Illumina [530011] 5 fat body mass, body mass index, obesity http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0001073 GCST001288 Genome-wide genotyping array 2008-08-21 17767159 Menzel S 2007-09-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17767159 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. F-cell distribution 179 European ancestry individuals 90 European ancestry individuals Illumina [308015] 3 fetal hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004576 GCST000069 Genome-wide genotyping array 2010-10-12 20862305 Shu XO 2010-09-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20862305 Identification of new genetic risk variants for type 2 diabetes. Type 2 diabetes 1,019 Chinese ancestry cases, 1,710 Chinese ancestry controls 2,591 European ancestry cases, 3,052 European ancestry controls, 6,184 East Asian cases, 9,853 East Asian controls Affymetrix [590887] 4 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000796 Genome-wide genotyping array 2014-01-07 21041247 Perlis RH 2010-11-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/21041247 Genome-wide association study of suicide attempts in mood disorder patients. Suicide risk 3,117 European ancestry Bipolar disorder cases, 1,273 European ancestry Major depressive disorder cases 2,698 European ancestry Bipolar disorder cases, 1,649 Major depressive disorder cases Affymetrix [1922309] (imputed) 4 mental or behavioural disorder, attempted suicide http://www.ebi.ac.uk/efo/EFO_0000677, http://www.ebi.ac.uk/efo/EFO_0004321 GCST000854 Genome-wide genotyping array 2008-07-11 18587394 Barrett JC 2008-06-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18587394 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. Crohn's disease 3,230 European ancestry cases, 4,829 European ancestry controls 1,339 European ancestry trios, 2,325 European ancestry cases, 1,809 European ancestry controls Affymetrix, Illumina [635547] (imputed) 30 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000207 Genome-wide genotyping array 2008-06-23 17846125 Hanson RL 2007-09-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/17846125 A search for variants associated with young-onset type 2 diabetes in American Indians in a 100K genotyping array. Type 2 diabetes 440 American Indian ancestry cases, 455 American Indian ancestry controls 1,207 American Indian ancestry cases, 1,627 American Indian ancestry controls, 1,465 European ancestry individuals, 427 European ancestry controls, 760 Hispanic individuals Affymetrix [80044] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000074 Genome-wide genotyping array 2010-01-07 20039944 Docherty SJ 2009-11-10 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/20039944 A genome-wide association study identifies multiple loci associated with mathematics ability and disability. Mathematical ability 600 European ancestry high-performing children, 600 European ancestry low-performing children 1,954 European ancestry children Affymetrix [358948] 0 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST000524 Genome-wide genotyping array 2009-09-28 17478681 McPherson R 2007-05-03 Science www.ncbi.nlm.nih.gov/pubmed/17478681 A common allele on chromosome 9 associated with coronary heart disease. Coronary heart disease 322 European ancestry cases, 312 European ancestry controls 3,984 European ancestry cases, 19,807 European ancestry controls Perlegen [72864] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000031 Genome-wide genotyping array 2009-06-17 19503088 Gregersen PK 2009-06-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19503088 REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. Rheumatoid arthritis 2,418 European ancestry cases, 4,504 European ancestry controls 2,604 cases, 2,882 controls Illumina [278502] 5 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000420 Genome-wide genotyping array 2008-06-16 17486107 Baum AE 2007-05-08 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/17486107 A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. Bipolar disorder 461 European ancestry cases, 563 European ancestry controls 772 European ancestry cases, 876 European ancestry controls Illumina [555235] 1 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000033 Genome-wide genotyping array 2009-02-27 19188921 Liu YZ 2009-02-03 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19188921 Genome-wide association analyses suggested a novel mechanism for smoking behavior regulated by IL15. Smoking behavior 417 European ancestry male individuals, 423 European ancestry female individuals 412 African American male individuals and 839 African American female individuals from 402 families, 3,491 European ancestry male individuals and 4,132 European ancestry female individuals from 1,731 families Affymetrix [379319] 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST000332 Genome-wide genotyping array 2011-03-01 21245432 Spraggs CF 2011-01-24 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/21245432 HLA-DQA1*02:01 is a major risk factor for lapatinib-induced hepatotoxicity in women with advanced breast cancer. Lapatinib-induced hepatotoxicity in breast cancer 26 European ancestry cases, 11 cases, 196 European ancestry controls, 90 controls 21 European ancestry cases, 3 cases, 123 European ancestry controls, 32 controls Illumina [1111203] 0 response to lapatinib http://purl.obolibrary.org/obo/GO_0036274 GCST000953 Genome-wide genotyping array 2011-01-15 21150874 McDonough CW 2010-12-08 Kidney Int www.ncbi.nlm.nih.gov/pubmed/21150874 A genome-wide association study for diabetic nephropathy genes in African Americans. Type 2 diabetes nephropathy 965 African American cases, 1,029 African American controls 709 African American cases, 690 African American controls Affymetrix [832357] 5 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST000909 Genome-wide genotyping array 2011-04-13 21437268 McKay JD 2011-03-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21437268 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. Oral cavity and pharyngeal cancer 2,091 European ancestry cases, 8,334 European ancestry controls 6,574 European ancestry cases, 7,892 European ancestry controls Illumina [294620] 5 upper aerodigestive tract neoplasm http://www.ebi.ac.uk/efo/EFO_0004284 GCST001011 Genome-wide genotyping array 2010-10-15 20884846 Yang Q 2010-09-30 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20884846 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. Urate levels 28,283 European ancestry individuals 22,054 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 11 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST000818 Genome-wide genotyping array 2009-06-14 19478819 Ng CC 2009-05-29 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19478819 A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. Nasopharyngeal carcinoma 111 Malaysian Chinese ancestry cases, 260 Malaysian Chinese ancestry controls 168 Malaysian Chinese ancestry cases, 252 Malaysian Chinese ancestry controls Illumina [533048] 1 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST000413 Genome-wide genotyping array 2010-03-07 20159113 Jakkula E 2010-02-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20159113 Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. Multiple sclerosis 68 Finland founder cases, 136 Finland founder controls 83 Finland founder cases, 365 Finland founder controls 3,285 European ancestry cases, 6,379 European ancestry controls, 1,202 cases, 3,399 controls Illumina [297343] 2 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000593 Genome-wide genotyping array 2011-01-03 21044949 Yang J 2010-11-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21044949 ELF1 is associated with systemic lupus erythematosus in Asian populations. Systemic lupus erythematosus 612 Chinese ancestry cases, 1,160 Chinese ancestry controls 2,090 Chinese ancestry cases, 1,981 Chinese ancestry controls, 462 Thai ancestry cases, 951 Thai ancestry controls Illumina [513108] 1 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000858 Genome-wide genotyping array 2008-11-12 18849993 Stacey SN 2008-10-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18849993 Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. Basal cell carcinoma 930 European ancestry cases, 33,117 European ancestry controls 1,216 European ancestry cases, 2,844 European ancestry controls Illumina [304083] 2 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST000249 Genome-wide genotyping array 2009-10-05 19767754 Gudmundsson J 2009-09-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19767754 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. Prostate cancer Up to 1,968 European ancestry cases, 35,382 European ancestry controls Up to 11,806 European ancestry cases, 12,387 European ancestry controls Illumina [310520] 8 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000489 Genome-wide genotyping array 2011-05-13 21497890 Orange JS 2011-04-15 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/21497890 Genome-wide association identifies diverse causes of common variable immunodeficiency. Common variable immunodeficiency 179 European ancestry cases, 1,917 European ancestry controls 109 European ancestry cases, 1,114 European ancestry controls Illumina [610000] 0 common variable immunodeficiency http://purl.obolibrary.org/obo/MONDO_0015517 GCST001039 Genome-wide genotyping array 2015-05-15 21353194 Cichon S 2011-02-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21353194 Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Bipolar disorder 682 European ancestry cases, 1,300 European ancestry controls 7,759 European ancestry cases, 34,062 European ancestry controls Illumina [511978] 1 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000985 Genome-wide genotyping array 2009-09-28 18193045 Sanna S 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193045 Common variants in the GDF5-UQCC region are associated with variation in human height. Height 1,084 European ancestry cases, 1,287 European ancestry controls, 4,298 European individuals 23,684 European ancestry individuals, 3,860 African American individuals Affymetrix, Illumina [~ 2261000] (imputed) 5 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000136 Genome-wide genotyping array 2008-06-16 18193046 Kooner JS 2008-01-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18193046 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. Triglycerides 1,005 European ancestry male individuals, 1,006 Indian Asian ancestry male individuals 6,827 European ancestry individuals, 2,528 Mexican ancestry individuals, 1,181 Indian Asian ancestry female individuals Perlegen [up to 216774] 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000137 Genome-wide genotyping array 2012-01-14 20600896 Engelman CD 2010-06-26 J Steroid Biochem Mol Biol www.ncbi.nlm.nih.gov/pubmed/20600896 Genome-wide association study of vitamin D concentrations in Hispanic Americans: the IRAS family study. Vitamin D levels 229 Hispanic individuals from 34 families 961 Hispanic individuals Illumina [309200] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST000711 Genome-wide genotyping array 2013-06-14 23382691 Lauc G 2013-01-31 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23382691 Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. IgG glycosylation 2,247 European ancestry individuals NA Illumina [~ 2500000] (imputed) 693 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST001848 Genome-wide genotyping array 2013-06-14 23382691 Lauc G 2013-01-31 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23382691 Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. IgG glycosylation 1,848 European ancestry individuals NA Illumina [~ 2500000] (imputed) 6 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST001849 Genome-wide genotyping array 2009-05-07 18821565 Lasky-Su J 2008-12-05 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18821565 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. Inattentive symptoms 930 European ancestry trios NA Perlegen [429981] 15 behavior http://purl.obolibrary.org/obo/GO_0007610 GCST000279 Genome-wide genotyping array 2009-05-07 18821565 Lasky-Su J 2008-12-05 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18821565 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. Hyperactive-impulsive symptoms 930 European ancestry trios NA Perlegen [429981] 14 behavior http://purl.obolibrary.org/obo/GO_0007610 GCST000278 Genome-wide genotyping array 2009-05-07 18821565 Lasky-Su J 2008-12-05 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18821565 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. Attention deficit hyperactivity disorder 930 European ancestry trios NA Perlegen [429981] 19 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST000281 Genome-wide genotyping array 2012-01-10 22174901 Chan KY 2011-12-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/22174901 Genome-wide association study of hepatocellular carcinoma in Southern Chinese patients with chronic hepatitis B virus infection. Hepatocellular carcinoma 95 Chinese ancestry HBV-infected cases, 97 Chinese ancestry HBV infected controls 500 Chinese ancestry HBV-infected cases, 728 Chinese ancestry HBV-infected controls Illumina [485072] 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST001348 Genome-wide genotyping array 2013-04-27 23358156 Benyamin B 2013-01-29 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23358156 Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Intelligence (childhood) 12,441 European ancestry children 5,548 European ancestry children Affymetrix, Illumina [138093] (imputed) 6 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST001837 Genome-wide genotyping array 2011-01-12 21124946 Paternoster L 2010-11-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21124946 Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone. Bone mineral density 1,934 European ancestry individuals Up to 3,835 European ancestry individuals Illumina [2417199] (imputed) 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000877 Genome-wide genotyping array 2010-05-24 20418888 Thorgeirsson TE 2010-04-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20418888 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Smoking behavior 31,266 European ancestry individuals 54,731 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 5 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST000667 Genome-wide genotyping array 2009-05-07 19412175 Capasso M 2009-05-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19412175 Common variations in BARD1 influence susceptibility to high-risk neuroblastoma. Neuroblastoma (high-risk) 397 European ancestry cases, 2,043 European ancestry controls 371 European ancestry cases, 2,119 European ancestry controls Illumina [462866] 1 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST000384 Genome-wide genotyping array 2012-01-24 21254220 Jiang Y 2011-02-01 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/21254220 Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder. Bipolar disorder 1,868 European ancestry cases, 2,938 European ancestry controls NA Affymetrix [NR] 24 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000961 Genome-wide genotyping array 2009-03-30 19260139 Polasek O 2009-02-01 Croat Med J www.ncbi.nlm.nih.gov/pubmed/19260139 Genome-wide association study of anthropometric traits in Korcula Island, Croatia. Anthropometric traits 898 Korculan (founder/genetic isolate) individuals NA Illumina [316730] 13 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST000327 Genome-wide genotyping array 2015-05-26 21314694 Kendler KS 2011-02-11 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/21314694 Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. Alcohol dependence 2,357 European ancestry individuals, 812 African American individuals NA Affymetrix [NR] 3 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST000977 Genome-wide genotyping array 2008-07-11 18576341 Behrens EM 2008-06-24 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/18576341 Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis. Arthritis (juvenile idiopathic) 67 European ancestry cases, 1,952 European ancestry controls, 63 cases NA Illumina [524684] 1 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST000206 Genome-wide genotyping array 2010-12-16 21060863 Ikram MK 2010-10-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21060863 Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. Retinal vascular caliber 15,358 European ancestry individuals 6,652 European ancestry individuals Affymetrix, Illumina [2194468] (imputed) 5 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST000847 Genome-wide genotyping array 2009-06-19 19508998 Knauff EA 2009-06-09 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/19508998 Genome-wide association study in premature ovarian failure patients suggests ADAMTS19 as a possible candidate gene. Premature ovarian failure 99 European ancestry cases, 235 European ancestry controls 60 European ancestry cases, 90 European ancestry controls Illumina [309158] 0 primary ovarian insufficiency http://www.ebi.ac.uk/efo/EFO_0004266 GCST000422 Genome-wide genotyping array 2009-06-01 19448622 Sulem P 2009-05-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19448622 Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche. Menarche (age at onset) 15,297 European ancestry female individuals 10,040 European ancestry female individuals Illumina [304226] 1 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST000400 Genome-wide genotyping array 2012-01-14 22180457 Kiyotani K 2011-12-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22180457 A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese. Response to tamoxifen in breast cancer 240 Japanese ancestry female cases 222 Japanese ancestry female cases Illumina [470796] 1 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST001357 Genome-wide genotyping array 2008-06-16 17804836 Plenge RM 2007-09-05 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/17804836 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. Rheumatoid arthritis 1,522 European ancestry cases, 1,850 European ancestry controls 1,053 European ancestry cases, 1,858 European ancestry controls Illumina [297086] 3 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000070 Genome-wide genotyping array 2008-06-16 17401366 Gudmundsson J 2007-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17401366 Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. Prostate cancer 1,453 European ancestry cases, 3,064 European ancestry controls 1,210 European ancestry cases, 2,445 European ancestry controls, 373 African American cases, 372 African American controls Illumina [316515] 3 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000019 Genome-wide genotyping array 2013-09-25 20064070 Herbeck JT 2010-02-15 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/20064070 Multistage genomewide association study identifies a locus at 1q41 associated with rate of HIV-1 disease progression to clinical AIDS. HIV-1 progression 51 European ancestry rapid progressor male cases, 57 European ancestry moderate progressor male cases, 48 European ancestry long-term progressor male cases 590 European ancestry seroconverter male cases Affymetrix [345926] 1 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST000596 Genome-wide genotyping array 2008-06-16 17529973 Hunter DJ 2007-05-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17529973 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Breast cancer 1,145 European ancestry cases, 1,142 European ancestry controls 874 European ancestry cases, 1,478 European ancestry controls, 302 cases, 594 controls Illumina [528173] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000036 Genome-wide genotyping array 2008-06-16 17554300 Wellcome Trust Case Control Consortium 2007-06-07 Nature www.ncbi.nlm.nih.gov/pubmed/17554300 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Crohn's disease 1,748 European ancestry cases, 2,938 European ancestry controls (see Parkes 2007) Affymetrix [469557] 13 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000042 Genome-wide genotyping array 2008-06-16 17554300 Wellcome Trust Case Control Consortium 2007-06-07 Nature www.ncbi.nlm.nih.gov/pubmed/17554300 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Hypertension 1,952 European ancestry cases, 2,938 European ancestry controls NA Affymetrix [469557] 2 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST000041 Genome-wide genotyping array 2008-06-16 17554300 Wellcome Trust Case Control Consortium 2007-06-07 Nature www.ncbi.nlm.nih.gov/pubmed/17554300 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Type 2 diabetes 1,924 European ancestry cases, 2,938 European ancestry controls (see Zeggini 2007) Affymetrix [469557] 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000047 Genome-wide genotyping array 2008-06-16 17554300 Wellcome Trust Case Control Consortium 2007-06-07 Nature www.ncbi.nlm.nih.gov/pubmed/17554300 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Rheumatoid arthritis 1,860 European ancestry cases, 2,938 European ancestry controls NA Affymetrix [469557] 7 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000040 Genome-wide genotyping array 2008-06-16 17554300 Wellcome Trust Case Control Consortium 2007-06-07 Nature www.ncbi.nlm.nih.gov/pubmed/17554300 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Coronary heart disease 1,926 European ancestry cases, 2,938 European ancestry controls (see Samani 2007) Affymetrix [469557] 4 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000045 Genome-wide genotyping array 2008-06-16 17554300 Wellcome Trust Case Control Consortium 2007-06-07 Nature www.ncbi.nlm.nih.gov/pubmed/17554300 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Bipolar disorder 1,868 European ancestry cases, 2,938 European ancestry controls NA Affymetrix [469557] 7 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000044 Genome-wide genotyping array 2008-06-16 17554300 Wellcome Trust Case Control Consortium 2007-06-07 Nature www.ncbi.nlm.nih.gov/pubmed/17554300 Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Type 1 diabetes 1,963 European ancestry cases, 2,938 European ancestry controls (see Todd 2007) Affymetrix [469557] 10 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000043 Genome-wide genotyping array 2011-05-26 21533175 Zhai G 2011-04-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21533175 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. Dehydroepiandrosterone sulphate levels 14,846 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST001038 Genome-wide genotyping array 2008-06-16 17634447 Stefansson H 2007-07-19 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/17634447 A genetic risk factor for periodic limb movements in sleep. Restless legs syndrome 306 European ancestry cases, 15,664 European ancestry controls 311 European ancestry cases, 1,895 European ancestry controls Illumina [306937] 1 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST000058 Genome-wide genotyping array 2011-12-20 22116812 Schrijvers EM 2011-11-23 Stroke www.ncbi.nlm.nih.gov/pubmed/22116812 Genome-wide association study of vascular dementia. Vascular dementia 67 European ancestry cases, 5,633 European ancestry controls 256 European ancestry cases, 5,839 European ancestry controls Illumina [528127] 0 GCST001328 Genome-wide genotyping array 2015-05-23 21307088 Khor CC 2011-02-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21307088 Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area. Optic disc area 2,132 Indian ancestry individuals, 2,313 Malay ancestry individuals 9,326 European ancestry individuals Illumina [551808] 4 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST000970 Genome-wide genotyping array 2010-03-29 20190752 Dubois PC 2010-02-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20190752 Multiple common variants for celiac disease influencing immune gene expression. Celiac disease 4,533 European ancestry cases, 10,750 European ancestry controls 4,918 European ancestry cases, 5,684 European ancestry controls Illumina [292387] 40 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST000612 Genome-wide genotyping array 2013-11-29 23722424 Rietveld CA 2013-05-30 Science www.ncbi.nlm.nih.gov/pubmed/23722424 GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Educational attainment up to 101,069 European ancestry individuals 25,490 European ancestry individuals Affymetrix, Illumina, Perlegen [up to 2309290] (imputed) 9 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST002045 Genome-wide genotyping array 2013-12-01 23722424 Rietveld CA 2013-05-30 Science www.ncbi.nlm.nih.gov/pubmed/23722424 GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Educational attainment (college completion) up to 126,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 23218963] (imputed) 1 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST002047 Genome-wide genotyping array 2019-08-09 23722424 Rietveld CA 2013-05-30 Science www.ncbi.nlm.nih.gov/pubmed/23722424 GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Educational attainment (years of education) up to 126,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 23218963] (imputed) 3 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST008396 Genome-wide genotyping array 2008-07-11 18594024 Sarasquete ME 2008-07-01 Blood www.ncbi.nlm.nih.gov/pubmed/18594024 Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis. Osteonecrosis of the jaw 22 European ancestry cases, 65 European ancestry controls NA Affymetrix [339972] 1 osteonecrosis http://www.ebi.ac.uk/efo/EFO_0004259 GCST000209 Genome-wide genotyping array 2009-05-19 19419973 Sanna S 2009-05-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19419973 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. Bilirubin levels 4,300 Sardinian individuals 1,860 Sardinian individuals, 832 Old Order Amish individuals Affymetrix [362129] 3 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST000388 Genome-wide genotyping array 2009-11-09 19838193 Han JW 2009-10-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19838193 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. Systemic lupus erythematosus 1,047 Han Chinese ancestry cases, 1,205 Han Chinese ancestry controls 3,152 Han Chinese ancestry cases, 7,050 Han Chinese ancestry controls Illumina [493955] 18 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000507 Genome-wide genotyping array 2008-11-26 18978792 Cooper JD 2008-11-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18978792 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. Type 1 diabetes 3,561 European ancestry cases, 4,646 European ancestry controls 6,225 European ancestry cases, 6,946 European ancestry controls, 3,064 European ancestry trios from 2,828 families Affymetrix [up to 335565] 14 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000258 Genome-wide genotyping array 2010-12-09 21079520 Sato Y 2010-11-12 J Thorac Oncol www.ncbi.nlm.nih.gov/pubmed/21079520 Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel. Non-small cell lung cancer (survival) 105 East Asian ancestry cases NA Illumina [109365] 3 survival time, non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0003060 GCST000871 Genome-wide genotyping array 2009-12-10 19915576 Satake W 2009-11-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19915576 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Parkinson's disease 988 Japanese ancestry cases, 2,521 Japanese ancestry controls 933 Japanese ancestry cases, 15,753 Japanese ancestry controls Illumina [435470] 4 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000530 Genome-wide genotyping array 2015-05-12 21378095 Fox ER 2011-03-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21378095 Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study. Blood pressure 7,473 African American individuals 1,188 Sub-Saharan African individuals, 10,694 African American individuals, 69,899 European ancestry individuals Affymetrix [2500000] (imputed) 0 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST000997 Genome-wide genotyping array 2010-10-17 20864672 Waterworth DM 2010-09-23 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/20864672 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. Triglycerides up to 17,723 European ancestry individuals up to 37,774 European ancestry individuals, up to 9,665 Indian Asian ancestry individuals Affymetrix, Illumina, Perlegen [2155369] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000809 Genome-wide genotyping array 2010-10-17 20864672 Waterworth DM 2010-09-23 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/20864672 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. LDL cholesterol up to 17,723 European ancestry individuals up to 37,774 European ancestry individuals, up to 9,665 Indian Asian ancestry individuals Affymetrix, Illumina, Perlegen [2155369] (imputed) 11 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000807 Genome-wide genotyping array 2010-10-17 20864672 Waterworth DM 2010-09-23 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/20864672 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. HDL cholesterol up to 17,723 European ancestry individuals up to 37,774 European ancestry individuals, up to 9,665 Indian Asian ancestry individuals Affymetrix, Illumina, Perlegen [2155369] (imputed) 12 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000805 Genome-wide genotyping array 2011-04-29 21452313 Freudenberg J 2011-04-01 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/21452313 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. Rheumatoid arthritis 801 Korean ancestry cases, 757 Korean ancestry controls 718 Korean ancestry cases, 719 Korean ancestry controls Illumina [441398] 5 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST001022 Genome-wide genotyping array 2009-12-28 19961619 Castro-Giner F 2009-12-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/19961619 A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS). Atopy 75 European ancestry atopy and asthma cases, 75 European ancestry atopy only cases, 75 European ancestry controls 429 European ancestry atopy cases, 222 European ancestry controls Illumina [NR] 1 atopy http://www.ebi.ac.uk/efo/EFO_0002686 GCST000540 Genome-wide genotyping array 2009-09-28 17997608 Li S 2007-11-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/17997608 The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts. Urate levels 4,305 Sardinian individuals 1,301 European ancestry individuals Affymetrix [362129] 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST000123 Genome-wide genotyping array 2012-03-31 22219177 Tao S 2012-01-04 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/22219177 A genome-wide search for loci interacting with known prostate cancer risk-associated genetic variants. Prostate cancer (SNP x SNP interaction) 4,723 European ancestry cases, 4,792 European ancestry controls NA Affymetrix, Illumina [1117531] (imputed) 51 genetic variation, prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0004828, http://www.ebi.ac.uk/efo/EFO_0001663 GCST001370 Genome-wide genotyping array 2010-02-02 20062062 Reveille JD 2010-01-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20062062 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. Ankylosing spondylitis 2,053 European ancestry cases, 5,140 European ancestry controls 898 European ancestry cases, 1,518 European ancestry controls Illumina [288662] 9 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST000563 Genome-wide genotyping array 2010-03-25 20189245 Han S 2010-02-25 Leuk Res www.ncbi.nlm.nih.gov/pubmed/20189245 Genome-wide association study of childhood acute lymphoblastic leukemia in Korea. Acute lymphoblastic leukemia (childhood) 45 Korean ancestry cases, 48 Korean ancestry controls NA Affymetrix [681931] 0 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST000608 Genome-wide genotyping array 2010-03-25 20202923 Bierut LJ 2010-03-02 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/20202923 A genome-wide association study of alcohol dependence. Alcohol dependence 1,235 European ancestry cases, 1,433 European ancestry controls, 662 African American cases, 499 African American controls 219 European ancestry families, 35 African American families, 4 families, 487 European ancestry cases, 1,358 European ancestry controls Illumina [948658] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST000619 Genome-wide genotyping array 2010-01-08 20012890 Ronald A 2009-12-13 Behav Genet www.ncbi.nlm.nih.gov/pubmed/20012890 A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples. Social and non-social autistic-like traits 1,462 European ancestry individuals 3,494 European ancestry individuals Affymetrix [up to 435457] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST000543 Genome-wide genotyping array 2009-12-28 20010834 Repapi E 2009-12-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20010834 Genome-wide association study identifies five loci associated with lung function. Pulmonary function 20,288 European ancestry individuals up to 54,276 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 7 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST000544 Genome-wide genotyping array 2010-06-14 20463552 Wu C 2010-06-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/20463552 Genome-wide examination of genetic variants associated with response to platinum-based chemotherapy in patients with small-cell lung cancer. Response to platinum-based chemotherapy in small-cell lung cancer 245 Han Chinese ancestry cases 183 Han Chinese ancestry cases Affymetrix [265996] 0 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST000688 Genome-wide genotyping array 2014-04-26 24105470 Wu Y 2013-10-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24105470 A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2. Adiponectin levels 7,827 East Asian ancestry individuals 10,252 East Asian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 10 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST002233 Genome-wide genotyping array 2010-04-12 20303064 Houlihan LM 2010-03-18 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20303064 Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time. Activated partial thromboplastin time 1,431 European ancestry individuals NA Illumina [542050] 3 partial thromboplastin time http://www.ebi.ac.uk/efo/EFO_0004310 GCST000631 Genome-wide genotyping array 2009-02-28 19219042 Zheng W 2009-02-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19219042 Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. Breast cancer 1,505 Chinese ancestry cases, 1,522 Chinese ancestry controls 5,026 Chinese ancestry cases, 2,476 Chinese ancestry controls, 1,591 European ancestry cases, 1,466 European ancestry controls Affymetrix [up to 607728] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000343 Genome-wide genotyping array 2011-06-01 21507922 Ramsuran V 2011-05-01 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/21507922 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. Platelet count 115 African ancestry HIV-negative individuals NA Illumina [874956] 10 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST001061 Genome-wide genotyping array 2011-06-01 21507922 Ramsuran V 2011-05-01 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/21507922 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. Neutrophil count 115 African ancestry HIV-negative individuals NA Illumina [874956] 20 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST001059 Genome-wide genotyping array 2008-06-16 17068223 Duerr RH 2006-10-26 Science www.ncbi.nlm.nih.gov/pubmed/17068223 A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Inflammatory bowel disease 547 European ancestry cases, 548 European ancestry controls 1,151 cases from 595 families, 433 controls Illumina [308332] 1 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST000008 Genome-wide genotyping array 2011-05-25 21502966 Weber F 2011-04-19 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/21502966 Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients. Response to interferon beta therapy 178 European ancestry antibody-positive individuals, 184 European ancestry antibody-negative individuals 350 European ancestry antibody-positive individuals, 468 European ancestry antibody-negative individuals Illumina [~ 317000] 2 response to interferon-beta http://purl.obolibrary.org/obo/GO_0035456 GCST001043 Genome-wide genotyping array 2008-11-12 18834626 Dehghan A 2008-10-01 Lancet www.ncbi.nlm.nih.gov/pubmed/18834626 Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. Urate levels 11,847 European ancestry individuals 11,024 European ancestry individuals, 3,843 African American individuals Affymetrix, Illumina [up to 530683] 3 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST000242 Genome-wide genotyping array 2015-05-06 22158540 Wu C 2011-12-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22158540 Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations. Pancreatic cancer 981 Han Chinese ancestry cases, 1,991 Han Chinese ancestry controls 2,603 Han Chinese ancestry cases, 2,877 Han Chinese ancestry controls Affymetrix [666141] 11 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST001350 Genome-wide genotyping array 2009-06-14 19483681 Rapley EA 2009-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19483681 A genome-wide association study of testicular germ cell tumor. Testicular germ cell tumor 730 cases, 1,435 controls 571 cases, 1,806 controls Illumina [307666] 6 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST000414 Genome-wide genotyping array 2013-04-23 21418511 Deelen J 2011-03-21 Aging Cell www.ncbi.nlm.nih.gov/pubmed/21418511 Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited. Longevity 403 European ancestry cases, 1,670 European ancestry controls 1,578 European ancestry cases, 1,997 European ancestry controls, 2,168 cases, 3,915 controls Illumina [516721] 1 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST001013 Genome-wide genotyping array 2012-02-08 22229870 Karns R 2012-01-09 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/22229870 Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia. Uric acid levels 1,300 European ancestry individuals NA Affymetrix [2241249] (imputed) 6 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST001374 Genome-wide genotyping array 2015-05-23 21326860 Tsai FJ 2011-02-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/21326860 Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study. Kawasaki disease 250 Han Chinese ancestry cases, 446 Han Chinese ancestry controls 208 Han Chinese ancestry cases, 366 Han Chinese ancestry controls Affymetrix [723638] 2 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST000962 Genome-wide genotyping array 2011-04-13 21448238 Ligthart L 2011-03-30 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21448238 Meta-analysis of genome-wide association for migraine in six population-based European cohorts. Migraine 2,116 European ancestry cases, 7,318 European ancestry controls, 330 Dutch founder cases, 1,216 Dutch founder controls 2,957 European ancestry cases, 5,774 European ancestry controls Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 2 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST001019 Genome-wide genotyping array 2009-06-16 19488044 Smith EN 2009-06-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19488044 Genome-wide association study of bipolar disorder in European American and African American individuals. Bipolar disorder 1,001 European ancestry cases, 1,033 European ancestry controls, 345 African American cases, 670 African American controls 1,550 European ancestry individuals from 250 families, 1,263 European ancestry cases, 431 European ancestry controls Affymetrix [702044] 1 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000417 Genome-wide genotyping array 2009-04-22 19367585 Poduslo SE 2009-04-14 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/19367585 A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis. Aging 89 European ancestry and African American successfully aged individuals, 227 European ancestry Alzheimers cases NA Affymetrix [469218] 1 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST000378 Genome-wide genotyping array 2011-06-01 21502085 Troyer JL 2011-05-01 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/21502085 Genome-wide association study implicates PARD3B-based AIDS restriction. AIDS progression 755 European ancestry seroconverter cases NA Affymetrix [700022] 7 AIDS http://www.ebi.ac.uk/efo/EFO_0000765 GCST001060 Genome-wide genotyping array 2010-10-15 20877300 Perroud N 2010-09-28 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/20877300 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. Suicidal ideation 706 European ancestry individuals NA Illumina [539199] 4 suicidal ideation http://www.ebi.ac.uk/efo/EFO_0004320 GCST000816 Genome-wide genotyping array 2009-12-01 19880490 Tanaka T 2009-10-30 Blood www.ncbi.nlm.nih.gov/pubmed/19880490 A genome-wide association analysis of serum iron concentrations. Iron levels 1,919 European ancestry individuals 569 female indiviuals Illumina [475322] 1 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST000517 Genome-wide genotyping array 2012-01-25 20686565 Teslovich TM 2010-08-05 Nature www.ncbi.nlm.nih.gov/pubmed/20686565 Biological, clinical and population relevance of 95 loci for blood lipids. Triglycerides 96,598 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 32 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000758 Genome-wide genotyping array 2012-01-25 20686565 Teslovich TM 2010-08-05 Nature www.ncbi.nlm.nih.gov/pubmed/20686565 Biological, clinical and population relevance of 95 loci for blood lipids. Cholesterol, total 100,184 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 52 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST000760 Genome-wide genotyping array 2012-01-25 20686565 Teslovich TM 2010-08-05 Nature www.ncbi.nlm.nih.gov/pubmed/20686565 Biological, clinical and population relevance of 95 loci for blood lipids. LDL cholesterol 95,454 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 37 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000759 Genome-wide genotyping array 2012-01-25 20686565 Teslovich TM 2010-08-05 Nature www.ncbi.nlm.nih.gov/pubmed/20686565 Biological, clinical and population relevance of 95 loci for blood lipids. HDL cholesterol 99,900 European ancestry individuals NA Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 47 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000755 Genome-wide genotyping array 2013-11-16 23577725 Naj AC 2013-05-01 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23577725 Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis. Age-related macular degeneration 1,207 European ancestry cases, 686 European ancestry controls 122 European ancestry cases, 86 European ancestry controls Affymetrix [2543887] (imputed) 5 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST001986 Genome-wide genotyping array 2013-11-16 23577725 Naj AC 2013-05-01 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23577725 Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis. Age-related macular degeneration (smoking status interaction) 548 European ancestry ever smoking cases, 278 European ancestry ever smoking controls, 346 European ancestry never smoking cases, 247 European ancestry never smoking controls NA Affymetrix [2543887] (imputed) 3 smoking status measurement, age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0001365 GCST001990 Genome-wide genotyping array 2013-11-16 23577725 Naj AC 2013-05-01 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23577725 Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis. Age-related macular degeneration (extreme sampling) 720 European ancestry grade 5 cases, 513 European ancestry grade 1 controls 70 European ancestry grade 5 cases, 73 European ancestry grade 1 controls Affymetrix [2543887] (imputed) 3 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST001987 Genome-wide genotyping array 2011-01-16 21151128 Chen ZJ 2010-12-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21151128 Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3. Polycystic ovary syndrome 744 Han Chinese ancestry cases, 895 Han Chinese ancestry controls 3,338 Han Chinese ancestry cases, 5,792 Han Chinese ancestry controls Affymetrix [611633] 5 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST000914 Genome-wide genotyping array 2008-06-16 17827064 van Es MA 2007-09-07 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/17827064 ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study. Amyotrophic lateral sclerosis 461 European ancestry cases, 450 European ancestry controls 876 European ancestry cases, 906 European ancestry controls Illumina [311946] 1 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000072 Genome-wide genotyping array 2009-06-14 19454037 Arnett DK 2009-05-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/19454037 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. Left ventricular mass 101 European ancestry cases, 101 European ancestry controls 704 European ancestry individuals, 1,467 African American individuals Affymetrix [96258] 2 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST000407 Genome-wide genotyping array 2011-12-20 22120009 Broderick P 2011-11-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22120009 Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk. Multiple myeloma 1,675 European ancestry cases, 5,903 European ancestry controls 169 European ancestry cases, 927 European ancestry controls Illumina [422839] 3 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST001331 Genome-wide genotyping array 2013-08-30 23594818 Ikeda M 2013-04-17 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/23594818 Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia. Psychosis (methamphetamine induced) 193 East Asian ancestry methamphetamine-dependent cases, 41 East Asian ancestry methamphetamine-dependent controls NA Affymetrix [244224] 1 methamphetamine-induced psychosis http://www.ebi.ac.uk/efo/EFO_0005242 GCST001975 Genome-wide genotyping array 2013-08-30 23594818 Ikeda M 2013-04-17 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/23594818 Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia. Methamphetamine dependence 236 Japanese ancestry cases, 864 Japanese ancestry controls NA Affymetrix [244224] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001972 Genome-wide genotyping array 2008-09-12 18073375 Duggan D 2007-12-19 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/18073375 Two genome-wide association studies of aggressive prostate cancer implicate putative prostate tumor suppressor gene DAB2IP. Prostate cancer 1,235 European ancestry cases, 1,599 European ancestry controls 1,032 European ancestry cases, 571 European ancestry controls, 210 African American cases, 346 African American controls Affymetrix, Illumina [60275] 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000128 Genome-wide genotyping array 2008-06-16 18075462 Suzuki S 2007-11-17 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/18075462 A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis. Coronary spasm 50 Japanese ancestry female cases, 50 Japanese ancestry female controls 151 Japanese ancestry female cases, 160 Japanese ancestry female controls Affymetrix [97552] 1 Coronary Vasospasm http://www.ebi.ac.uk/efo/EFO_0004225 GCST000125 Genome-wide genotyping array 2008-10-14 18760390 Huyghe JR 2008-09-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18760390 Genome-wide SNP-based linkage scan identifies a locus on 8q24 for an age-related hearing impairment trait. Hearing impairment 1,081 European ancestry individuals from 200 sibships NA Affymetrix [169154] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST000230 Genome-wide genotyping array 2008-12-01 18940312 Yuan X 2008-10-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18940312 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. Liver enzyme levels 7,751 European ancestry individuals 1,005 European ancestry individuals, 3,669 Asian Indian ancestry individuals Affymetrix, Illumina [up to 496032] 11 liver enzyme measurement http://www.ebi.ac.uk/efo/EFO_0004582 GCST000248 Genome-wide genotyping array 2009-04-03 19330030 Thomas G 2009-03-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19330030 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). Breast cancer 1,145 European ancestry cases, 1,142 European ancestry controls 8,625 European ancestry cases, 9,657 European ancestry controls Illumina [528173] 6 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000365 Genome-wide genotyping array 2009-01-06 19023125 Potkin SG 2008-11-20 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/19023125 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. Brain imaging in schizophrenia (dorsolateral prefrontal cortex interaction) 46 European ancestry cases, 60 European ancestry controls, 18 cases, 14 controls NA Illumina [302783] 6 schizophrenia, dorsolateral prefrontal cortex functional measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008358 GCST000271 Genome-wide genotyping array 2008-09-10 17903306 Newton-Cheh C 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903306 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. Heart rate variability traits 747 European ancestry individuals from 307 families NA Affymetrix [70897] 2 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST000086 Genome-wide genotyping array 2009-09-28 17903306 Newton-Cheh C 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903306 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. Electrocardiographic traits 1,951 European ancestry individuals from 355 families NA Affymetrix [70897] 2 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST000111 Genome-wide genotyping array 2008-09-15 18159244 Hinney A 2007-12-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/18159244 Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants. Obesity (early onset extreme) 487 European ancestry cases, 442 European ancestry controls 2,269 European ancestry individuals from 644 families Affymetrix [440794] 1 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST000129 Genome-wide genotyping array 2010-09-24 20708005 Chalasani N 2010-08-10 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/20708005 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. Non-alcoholic fatty liver disease histology (lobular) 236 European ancestry cases NA Illumina [324623] 13 non-alcoholic fatty liver disease, cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0003095, http://www.ebi.ac.uk/efo/EFO_0001422 GCST000766 Genome-wide genotyping array 2010-09-24 20708005 Chalasani N 2010-08-10 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/20708005 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. Non-alcoholic fatty liver disease histology (other) 236 European ancestry cases NA Illumina [324623] 16 serum alanine aminotransferase measurement, non-alcoholic fatty liver disease, cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0003095, http://www.ebi.ac.uk/efo/EFO_0001422 GCST000765 Genome-wide genotyping array 2010-09-24 20708005 Chalasani N 2010-08-10 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/20708005 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. Non-alcoholic fatty liver disease histology (AST) 236 European ancestry cases NA Illumina [324623] 6 non-alcoholic fatty liver disease, cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0003095, http://www.ebi.ac.uk/efo/EFO_0001422 GCST000767 Genome-wide genotyping array 2008-09-10 17903297 Seshadri S 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903297 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. Volumetric brain MRI 705 European ancestry individuals NA Affymetrix [70897] 5 volumetric brain MRI http://www.ebi.ac.uk/efo/EFO_0004868 GCST000088 Genome-wide genotyping array 2008-09-10 17903297 Seshadri S 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903297 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. Cognitive test performance 694 European ancestry individuals NA Affymetrix [70897] 14 neuropsychological test http://www.ebi.ac.uk/efo/EFO_0003926 GCST000098 Genome-wide genotyping array 2008-06-16 17660530 Hafler DA 2007-07-29 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/17660530 Risk alleles for multiple sclerosis identified by a genomewide study. Multiple sclerosis 931 European ancestry trios, 2,431 European ancestry controls 609 European ancestry trios, 2,322 European ancestry cases, 2,987 European ancestry controls Affymetrix [334923] 6 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000062 Genome-wide genotyping array 2008-06-16 17052657 Fung HC 2006-09-28 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/17052657 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. Parkinson's disease 267 European ancestry cases, 270 European ancestry controls NA Illumina [408803] 3 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000005 Genome-wide genotyping array 2010-05-10 20364137 Yasuno K 2010-04-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20364137 Genome-wide association study of intracranial aneurysm identifies three new risk loci. Intracranial aneurysm 2,780 European ancestry cases, 12,515 European ancestry controls 3,111 Japanese ancestry cases, 1,666 Japanese ancestry controls Illumina [831534] (imputed) 6 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST000646 Genome-wide genotyping array 2010-05-18 20395239 Macgregor S 2010-04-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20395239 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Optic nerve measurement (cup area) 1,368 European ancestry twins from 666 families 848 European ancestry twins from 531 families Illumina [~ 2740000] (imputed) 9 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST000659 Genome-wide genotyping array 2010-05-18 20395239 Macgregor S 2010-04-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20395239 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Optic nerve measurement (rim area) 1,368 European ancestry twins from 666 families 848 European ancestry twins from 531 families Illumina [~ 2740000] (imputed) 6 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST000658 Genome-wide genotyping array 2010-05-18 20395239 Macgregor S 2010-04-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20395239 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Optic nerve measurement (disc area) 1,368 European ancestry twins from 666 families 848 European ancestry twins from 531 families Illumina [~ 2740000] (imputed) 7 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST000657 Genome-wide genotyping array 2014-07-09 20395239 Macgregor S 2010-04-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20395239 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. Optic nerve measurement (cup-to-disc ratio) 1,368 European ancestry twins from 666 families 848 European ancestry twins from 531 families Illumina [~ 2740000] (imputed) 4 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST000655 Genome-wide genotyping array 2010-06-02 20453838 Turnbull C 2010-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20453838 Genome-wide association study identifies five new breast cancer susceptibility loci. Breast cancer 3,659 European ancestry cases, 4,897 European ancestry controls 12,576 European ancestry cases, 12,223 European ancestry controls Illumina [582886] 13 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000678 Genome-wide genotyping array 2009-09-09 19724244 Laje G 2009-08-31 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/19724244 Genome-wide association study of suicidal ideation emerging during citalopram treatment of depressed outpatients. Response to antidepressant treatment 90 Hispanic and European ancestry cases, 90 Hispanic and European ancestry controls 30 Hispanic and European ancestry cases, 1,652 Hispanic and European ancestry controls Illumina [100864] 0 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST000470 Genome-wide genotyping array 2011-05-24 21471458 Schumann G 2011-04-06 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/21471458 Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. Alcohol consumption 26,316 European ancestry individuals 21,185 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 1 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST001029 Genome-wide genotyping array 2008-09-10 17903303 O'Donnell CJ 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903303 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. Subclinical atherosclerosis traits (other) Up to 984 individuals NA Affymetrix [70897] 8 cardiovascular disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005278 GCST000087 Genome-wide genotyping array 2008-09-10 17903303 O'Donnell CJ 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903303 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. Coronary artery calcification Up to 678 individuals NA Affymetrix [70897] 3 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST000097 Genome-wide genotyping array 2010-05-26 20442857 Suchindran S 2010-04-29 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20442857 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. Lipoprotein-associated phospholipase A2 activity and mass 6,668 European ancestry individuals NA Affymetrix [360811] 5 lipoprotein-associated phospholipase A(2) measurement http://www.ebi.ac.uk/efo/EFO_0004746 GCST000671 Genome-wide genotyping array 2010-03-17 20215924 Liu X 2010-01-01 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/20215924 A genome-wide association study of amygdala activation in youths with and without bipolar disorder. Functional MRI 36 European ancestry BD cases, 21 European ancestry controls, 1 African American BD case, 5 African American controls, 2 BD cases, 3 controls NA Illumina [104043] 2 amygdala reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004550 GCST000556 Genome-wide genotyping array 2009-09-28 17053149 Papassotiropoulos A 2006-10-20 Science www.ncbi.nlm.nih.gov/pubmed/17053149 Common Kibra alleles are associated with human memory performance. Memory performance 341 European ancestry individuals 662 European ancestry individuals, 18 Hispanic, African American, Native American, and Asian ancestry individuals Affymetrix [178390] 0 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST000007 Genome-wide genotyping array 2009-09-29 19736353 Ising M 2009-09-01 Arch Gen Psychiatry www.ncbi.nlm.nih.gov/pubmed/19736353 A genomewide association study points to multiple loci that predict antidepressant drug treatment outcome in depression. Response to antidepressant treatment 700 European ancestry cases 832 European ancestry cases, 366 European ancestry controls Illumina [389251] 0 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST000471 Genome-wide genotyping array 2010-07-16 20585627 Eriksson N 2010-06-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20585627 Web-based, participant-driven studies yield novel genetic associations for common traits. Hair color 9,126 European ancestry individuals NA Illumina [535076] 12 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST000707 Genome-wide genotyping array 2010-07-16 20585627 Eriksson N 2010-06-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20585627 Web-based, participant-driven studies yield novel genetic associations for common traits. Freckling 9,126 European ancestry individuals NA Illumina [535076] 4 freckles http://www.ebi.ac.uk/efo/EFO_0003963 GCST000708 Genome-wide genotyping array 2010-07-16 20585627 Eriksson N 2010-06-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20585627 Web-based, participant-driven studies yield novel genetic associations for common traits. Common traits (Other) 9,126 European ancestry individuals NA Illumina [535076] 16 sensory perception of taste, functional laterality, hair morphology, circadian rhythm, personality, braces, sensory perception of smell, Attached earlobe, Astigmatism, Sneeze http://purl.obolibrary.org/obo/GO_0050909, http://www.ebi.ac.uk/efo/EFO_0003889, http://www.ebi.ac.uk/efo/EFO_0005038, http://www.ebi.ac.uk/efo/EFO_0004354, http://www.ebi.ac.uk/efo/EFO_0003947, http://www.ebi.ac.uk/efo/EFO_0004291, http://purl.obolibrary.org/obo/GO_0007608, http://purl.obolibrary.org/obo/HP_0009907, http://purl.obolibrary.org/obo/HP_0000483, http://purl.obolibrary.org/obo/HP_0025095 GCST000706 Genome-wide genotyping array 2010-07-16 20585627 Eriksson N 2010-06-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20585627 Web-based, participant-driven studies yield novel genetic associations for common traits. Eye color 9,126 European ancestry individuals NA Illumina [535076] 8 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST000710 Genome-wide genotyping array 2009-02-06 19169254 Nair RP 2009-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19169254 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. Psoriasis 1,359 European ancestry cases, 1,400 European ancestry controls 5,048 European ancestry cases, 5,041 European ancestry controls Perlegen [~ 2500000] (imputed) 8 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST000322 Genome-wide genotyping array 2013-04-24 21483845 McLaren CE 2011-03-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/21483845 Genome-wide association study identifies genetic loci associated with iron deficiency. Iron status biomarkers 336 European ancestry iron deficiency cases, 343 European ancestry controls 71 European ancestry iron deficiency cases, 161 European ancestry controls Illumina [331060] 9 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST001021 Genome-wide genotyping array 2013-04-24 21483845 McLaren CE 2011-03-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/21483845 Genome-wide association study identifies genetic loci associated with iron deficiency. Iron deficiency 336 European ancestry cases, 343 European ancestry controls 71 European ancestry cases, 161 European ancestry controls Illumina [331060] 1 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST001020 Genome-wide genotyping array 2015-05-27 21339755 Liu X 2011-02-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21339755 A non-synonymous polymorphism in galactose mutarotase (GALM) is associated with serotonin transporter binding potential in the human thalamus: results of a genome-wide association study. 5-HTT brain serotonin transporter levels 16 European, African American and Hispanic unmedicated bipolar disorder cases, 17 European, African American and Hispanic unmedicated major depressive disorder cases, 22 controls 51 European ancestry individuals Illumina [93247] 1 brain serotonin transporter measurement http://www.ebi.ac.uk/efo/EFO_0004569 GCST000983 Genome-wide genotyping array 2010-10-07 20852633 Bolton KL 2010-09-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20852633 Common variants at 19p13 are associated with susceptibility to ovarian cancer. Ovarian cancer 1,768 European ancestry cases, 2,353 European ancestry controls 8,739 European ancestry cases, 10,831 European ancestry controls Illumina [540573] 2 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST000800 Genome-wide genotyping array 2009-02-07 19169255 Zhang XJ 2009-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19169255 Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. Psoriasis 1,139 Han Chinese ancestry cases, 1,132 Han Chinese ancestry controls 5,721 Chinese ancestry cases, 7,340 Chinese ancestry controls Illumina [494902] 3 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST000321 Genome-wide genotyping array 2008-06-16 17690259 Thorleifsson G 2007-08-09 Science www.ncbi.nlm.nih.gov/pubmed/17690259 Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. Glaucoma (exfoliation) 75 European ancestry cases, 14,474 European ancestry controls 199 European ancestry cases, 198 European ancestry controls Illumina [304250] 1 exfoliation syndrome http://www.ebi.ac.uk/efo/EFO_0004235 GCST000067 Genome-wide genotyping array 2009-02-25 19182806 Stefansson H 2009-02-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19182806 Variant in the sequence of the LINGO1 gene confers risk of essential tremor. Essential tremor 452 European ancestry cases, 14,378 European ancestry controls 301 European ancestry cases, 1,419 European ancestry controls Illumina [305624] 1 essential tremor http://www.ebi.ac.uk/efo/EFO_0003108 GCST000329 Genome-wide genotyping array 2012-09-20 22807686 Li S 2012-07-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22807686 GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers. Hepatocellular carcinoma 1,538 Han Chinese ancestry HBV-positive HCC cases, 1,465 Han Chinese ancestry chronic HBV carriers 4,431 Han Chinese ancestry HBV-positive HCC cases, 4,725 Han Chinese ancestry chronic HBV carriers NR [523663] 3 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST001603 Genome-wide genotyping array 2010-07-01 20541252 Wang TJ 2010-06-09 Lancet www.ncbi.nlm.nih.gov/pubmed/20541252 Common genetic determinants of vitamin D insufficiency: a genome-wide association study. Vitamin D insufficiency 16,125 European ancestry individuals 17,871 European ancestry individuals Affymetrix, Illumina [up to 2548976] (imputed) 3 vitamin D deficiency http://www.ebi.ac.uk/efo/EFO_0003762 GCST000697 Genome-wide genotyping array 2013-08-13 23585552 Kirin M 2013-04-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23585552 Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment. Rhegmatogenous retinal detachment 867 European ancestry cases, 1,953 European ancestry controls 1,966 European ancestry cases, 5,918 European ancestry controls Illumina [299737] 4 rhegmatogenous retinal detachment http://www.ebi.ac.uk/efo/EFO_0005240 GCST001966 Genome-wide genotyping array 2011-05-11 21483430 Carless MA 2011-04-12 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21483430 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. Neuranatomic and neurocognitive phenotypes 857 Mexican American individuals NA Illumina [543031] 1 neuroimaging measurement, South Texas Assessment of Neurocognition http://www.ebi.ac.uk/efo/EFO_0004346, http://www.ebi.ac.uk/efo/EFO_0004785 GCST001037 Genome-wide genotyping array 2010-09-28 20802025 Tang W 2010-08-27 Blood www.ncbi.nlm.nih.gov/pubmed/20802025 Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. Protein C levels 8,048 European ancestry individuals 1,376 European ancestry individuals Affymetrix [2461269] 4 protein C measurement http://www.ebi.ac.uk/efo/EFO_0004633 GCST000780 Genome-wide genotyping array 2008-09-10 17903296 Kiel DP 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903296 Genome-wide association with bone mass and geometry in the Framingham Heart Study. Bone mineral density Up to 1,141 individuals from 241 families NA Affymetrix [70897] 8 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000092 Genome-wide genotyping array 2008-09-10 17903296 Kiel DP 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903296 Genome-wide association with bone mass and geometry in the Framingham Heart Study. Hip geometry Up to 1,094 individuals from 241 families NA Affymetrix [70897] 16 hip geometry http://www.ebi.ac.uk/efo/EFO_0004685 GCST000101 Genome-wide genotyping array 2010-05-11 20397748 Liu JZ 2010-04-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/20397748 Genome-wide association study of height and body mass index in Australian twin families. Body mass index 11,536 European ancestry individuals NA Illumina [559712] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000642 Genome-wide genotyping array 2010-05-11 20397748 Liu JZ 2010-04-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/20397748 Genome-wide association study of height and body mass index in Australian twin families. Height 11,536 European ancestry individuals NA Illumina [559712] (imputed) 8 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000644 Genome-wide genotyping array 2010-11-24 20947153 Ueta M 2010-10-12 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/20947153 Association between prostaglandin E receptor 3 polymorphisms and Stevens-Johnson syndrome identified by means of a genome-wide association study. Stevens-Johnson syndrome 60 Japanese ancestry cases, 300 Japanese ancestry controls 40 cases, 608 controls Affymetrix [313924] 0 Stevens-Johnson syndrome http://www.ebi.ac.uk/efo/EFO_0004276 GCST000832 Genome-wide genotyping array 2010-03-12 20172861 Okada Y 2010-02-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20172861 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. Neutrophil count 5,771 Japanese ancestry individuals 1,894 Japanese ancestry individuals Illumina [486091] 2 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST000600 Genome-wide genotyping array 2013-11-09 20592726 Chen SH 2010-06-30 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/20592726 Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 211 European ancestry child cases, 40 Black child cases, 46 Hispanic child cases, 4 Asian ancestry child cases, 21 child cases 99 European ancestry child cases, 33 Black child cases, 24 Hispanic child cases, 2 Asian ancestry child cases, 5 child cases Affymetrix [364033] 1 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST000715 Genome-wide genotyping array 2008-09-12 17903302 Levy D 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903302 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. Blood pressure Up to 1,327 individuals NA Affymetrix [70897] 9 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST000094 Genome-wide genotyping array 2008-06-18 17903302 Levy D 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903302 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. Tonometry 644 individuals NA Affymetrix [70897] 13 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST000107 Genome-wide genotyping array 2015-04-19 21263130 Fletcher O 2011-01-24 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/21263130 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. Breast cancer 2,839 European ancestry cases, 3,507 European ancestry controls 9,041 European ancestry cases, 8,980 European ancestry controls Illumina [~ 296114] 9 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000952 Genome-wide genotyping array 2009-11-05 19820698 Chambers JC 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19820698 Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. Hemoglobin 6,316 European ancestry individuals, 9,685 Indian Asian ancestry individuals 5,187 European ancestry individuals, 6,721 Indian Asian ancestry individuals Affymetrix, Illumina, Perlegen [NR] 2 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST000501 Genome-wide genotyping array 2010-09-28 20832056 Ikeda M 2010-09-08 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20832056 Genome-wide association study of schizophrenia in a Japanese population. Schizophrenia 560 Japanese ancestry cases, 548 Japanese ancestry controls 1,511 Japanese ancestry cases, 2,451 Japanese ancestry controls, 479 European ancestry cases, 2,938 European ancestry controls Affymetrix [297645] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000788 Genome-wide genotyping array 2015-05-28 21316860 Velders FP 2011-02-11 Psychoneuroendocrinology www.ncbi.nlm.nih.gov/pubmed/21316860 Genetics of cortisol secretion and depressive symptoms: a candidate gene and genome wide association approach. Cortisol secretion 1,711 European ancestry individuals 2,836 European ancestry individuals Illumina [530683] 0 cortisol secretion measurement http://www.ebi.ac.uk/efo/EFO_0004642 GCST000978 Genome-wide genotyping array 2009-09-28 17671248 Dunckley T 2007-08-01 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/17671248 Whole-genome analysis of sporadic amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 386 European ancestry cases, 542 European ancestry controls 901 cases and 1,025 controls of European, Hispanic, Asian, American Indian, Pacific Islander, and other ancestries Affymetrix, Illumina [776955] 0 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000065 Genome-wide genotyping array 2009-11-05 19820699 Benyamin B 2009-10-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19820699 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. Iron status biomarkers 4,818 European ancestry individuals 3,470 European ancestry individuals Illumina, Perlegen [427037] 4 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST000505 Genome-wide genotyping array 2010-10-05 20825314 Baratz KH 2010-09-09 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/20825314 E2-2 protein and Fuchs's corneal dystrophy. Fuchs's corneal dystrophy 130 European ancestry cases, 260 European ancestry controls 150 cases, 150 controls Illumina [~ 370000] 2 Fuchs endothelial corneal dystrophy http://www.orpha.net/ORDO/Orphanet_98974 GCST000790 Genome-wide genotyping array 2011-01-18 21177773 Moyer AM 2010-12-22 Toxicol Sci www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. Response to acetaminophen (hepatotoxicity) 60 European ancestry lymphoblastoid cell lines, 56 African American lymphoblastoid cell lines, 60 Han Chinese American lymphoblastoid cell lines NA Affymetrix, Illumina [1348864] 5 response to paracetamol http://purl.obolibrary.org/obo/GO_1901554 GCST000924 Genome-wide genotyping array 2012-01-11 22174390 Rankinen T 2011-12-15 J Appl Physiol (1985) www.ncbi.nlm.nih.gov/pubmed/22174390 Heritability of submaximal exercise heart rate response to exercise training is accounted for by nine SNPs. Heart rate variability traits 472 European ancestry individuals from 99 families NA Illumina [320000] 2 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST001354 Genome-wide genotyping array 2011-03-29 21297633 Anderson CA 2011-02-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21297633 Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Ulcerative colitis 6,687 European ancestry cases, 19,718 European ancestry controls 9,628 European ancestry cases, 12,917 European ancestry controls Affymetrix, Illumina [~ 1100000] (imputed) 47 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000964 Genome-wide genotyping array 2013-04-17 23349640 Vijai J 2013-01-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23349640 Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. Lymphoma 275 Follicular non-Hodgkin's Lymphoma cases, 269 diffuse large B-cell non-Hodgkin's Lymphoma cases, 198 other non-Hodgkin's Lymphoma cases, 202 Hodgkin's Lymphoma cases, 4,044 controls 202 European ancestry Follicular non-Hodgkin's Lymphoma cases, 367 European ancestry diffuse large B-cell non-Hodgkin's Lymphoma cases, 577 European ancestry other non-Hodgkin's Lymphoma cases, 99 European ancestry Hodgkin's Lymphoma cases, 2,596 European ancestry controls Affymetrix [530583] 13 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST001826 Genome-wide genotyping array 2008-06-16 18204447 Kozyrev SV 2008-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18204447 Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. Systemic lupus erythematosus 279 European ancestry cases, 515 European ancestry controls 1,757 European ancestry cases, 1,540 European ancestry controls Affymetrix [85042] 1 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000143 Genome-wide genotyping array 2015-05-27 21294900 Charles BA 2011-02-04 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/21294900 A genome-wide association study of serum uric acid in African Americans. Uric acid levels 1,017 African American individuals NA Affymetrix [2366856] (imputed) 12 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST000963 Genome-wide genotyping array 2008-12-01 19011631 Houlston RS 2008-11-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19011631 Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. Colorectal cancer 1,902 European ancestry cases, 1,929 European ancestry controls 18,284 European ancestry cases, 18,926 European ancestry controls Illumina [up to 548586] 4 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000270 Genome-wide genotyping array 2012-01-20 22179738 Lai HM 2011-12-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/22179738 Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences. Gout 20 Han Chinese ancestry male gout cases, 42 Han Chinese ancestry male controls NA Illumina [479403] 36 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST001356 Genome-wide genotyping array 2009-12-04 19893584 Kim JJ 2009-11-06 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19893584 Identification of 15 loci influencing height in a Korean population. Height 8,842 Korean ancestry individuals NA Affymetrix [334546] 15 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000522 Genome-wide genotyping array 2014-07-01 21130132 Mick E 2010-12-01 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21130132 Genome-wide association study of blood pressure response to methylphenidate treatment of attention-deficit/hyperactivity disorder. Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) 140 child cases NA Affymetrix [316934] 7 response to methylphenidate http://purl.obolibrary.org/obo/GO_0036271 GCST000903 Genome-wide genotyping array 2010-11-23 20939080 Greenbaum L 2010-10-11 Mov Disord www.ncbi.nlm.nih.gov/pubmed/20939080 Evidence for association of the GLI2 gene with tardive dyskinesia in patients with chronic schizophrenia. Tardive dyskinesia in schizophrenia 88 European ancestry cases, 40 African American cases, 3 cases, 129 European ancestry controls, 62 African American controls, 5 controls 44 Ashkenazi Jewish Israeli cases, 33 Jewish Israeli cases, 52 Ashkenazi Jewish Israeli controls, 41 Jewish Israeli controls Perlegen [495172] 0 movement disorder http://www.ebi.ac.uk/efo/EFO_0004280 GCST000831 Genome-wide genotyping array 2009-03-01 19198610 Gudbjartsson DF 2009-02-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19198610 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Eosinophil counts 9,392 European ancestry individuals 12,118 European ancestry individuals, 5,212 East Asian ancestry individuals Illumina [312179] 7 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST000339 Genome-wide genotyping array 2009-03-31 19300500 Wilk JB 2009-03-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19300500 A genome-wide association study of pulmonary function measures in the Framingham Heart Study. Pulmonary function 7,691 European ancestry individuals 835 European ancestry individuals Affymetrix [2540223] (imputed) 1 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST000362 Genome-wide genotyping array 2009-04-02 19305409 Pfeufer A 2009-03-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19305409 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. QT interval 15,842 European ancestry individuals up to 13,602 individuals Affymetrix, Illumina [2557000] (imputed) 12 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST000364 Genome-wide genotyping array 2009-02-27 19207018 Kim H 2009-02-01 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/19207018 Genome-wide association study of acute post-surgical pain in humans. Pain 112 European ancestry individuals NA Affymetrix [374975] 3 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST000326 Genome-wide genotyping array 2013-04-17 23337848 Posti JP 2013-01-18 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/23337848 A polymorphism in the protein kinase C gene PRKCB is associated with α2-adrenoceptor-mediated vasoconstriction. Vascular constriction 64 European ancestry individuals 68 African America and European ancestry individuals Illumina [433378] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST001828 Genome-wide genotyping array 2009-05-07 18937294 Lasky-Su J 2008-12-05 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18937294 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. Attention deficit hyperactivity disorder (time to onset) 930 European ancestry trios NA Perlegen [429981] 11 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST000280 Genome-wide genotyping array 2011-04-04 21326311 Bhatnagar P 2011-02-17 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21326311 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. F-cell distribution in sickle cell anaemia 440 African American individuals NA Illumina [660740] 11 fetal hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004576 GCST000982 Genome-wide genotyping array 2008-06-16 16252231 Maraganore DM 2005-09-09 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/16252231 High-resolution whole-genome association study of Parkinson disease. Parkinson's disease 381 European ancestry cases, 363 European ancestry controls, 62 cases,79 controls, 1 Asian ancestry control from 443 sibships 269 European ancestry cases, 272 European ancestry controls, 62 cases, 60 controls, 1 Asian ancestry case Perlegen [198345] 1 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000002 Genome-wide genotyping array 2009-08-21 19197363 Need AC 2009-02-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19197363 A genome-wide investigation of SNPs and CNVs in schizophrenia. Schizophrenia 871 European ancestry cases, 863 European ancestry controls 1,460 European ancestry cases, 12,995 European ancestry controls Illumina [312565] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000336 Genome-wide genotyping array 2010-03-09 20154341 Lange LA 2010-02-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20154341 Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults. Homocysteine levels 1,786 Filipino ancestry female individuals 1,679 Filipino ancestry offspring Affymetrix [2073674] (imputed) 1 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST000594 Genome-wide genotyping array 2010-12-16 21082022 Padmanabhan S 2010-10-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21082022 Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. Hypertension 1,621 extreme cases, 1,699 controls 19,845 extreme cases, 16,541 controls Illumina [521220] (imputed) 1 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST000849 Genome-wide genotyping array 2010-07-12 20548946 Ramdas WD 2010-06-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20548946 A genome-wide association study of optic disc parameters. Vertical cup-disc ratio 7,360 European ancestry individuals 4,455 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 9 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST000700 Genome-wide genotyping array 2010-07-12 20548946 Ramdas WD 2010-06-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20548946 A genome-wide association study of optic disc parameters. Optic disc parameters 7,360 European ancestry individuals 4,455 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 3 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST000699 Genome-wide genotyping array 2011-01-09 21182207 Salyakina D 2010-12-01 Autism Res www.ncbi.nlm.nih.gov/pubmed/21182207 Variants in several genomic regions associated with asperger disorder. Asperger disorder 848 individuals from 232 families NA Illumina [439282] (imputed) 5 Asperger syndrome http://www.ebi.ac.uk/efo/EFO_0003757 GCST000904 Genome-wide genotyping array 2008-12-09 18985386 Pankratz N 2008-11-06 Hum Genet www.ncbi.nlm.nih.gov/pubmed/18985386 Genomewide association study for susceptibility genes contributing to familial Parkinson disease. Parkinson's disease (familial) 1,119 European ancestry cases, 1,127 European ancestry controls NA Illumina [328189] 1 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000261 Genome-wide genotyping array 2008-07-22 18360741 Butcher LM 2008-03-25 Behav Genet www.ncbi.nlm.nih.gov/pubmed/18360741 The nature of nurture: a genomewide association scan for family chaos. Environmental confusion in the home 469 European ancestry children from low chaos families, 369 European ancestry children from high chaos families 3,529 European ancestry children Affymetrix [117062] 0 CHAOS measure http://www.ebi.ac.uk/efo/EFO_0004779 GCST000166 Genome-wide genotyping array 2011-05-28 21529783 Heath AC 2011-04-27 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21529783 A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Alcoholism (heaviness of drinking) 2,062 European ancestry alcohol dependence cases, 6,692 European ancestry controls 3,393 European ancestry individuals Illumina [~ 300000] 8 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001052 Genome-wide genotyping array 2011-05-28 21529783 Heath AC 2011-04-27 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21529783 A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Alcoholism (12-month weekly alcohol consumption) 2,062 European ancestry alcohol dependence cases, 6,692 European ancestry controls 3,393 European ancestry individuals Illumina [~ 300000] 2 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001055 Genome-wide genotyping array 2011-05-28 21529783 Heath AC 2011-04-27 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21529783 A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Alcoholism (alcohol use disorder factor score) 2,062 European ancestry alcohol dependence cases, 6,692 European ancestry controls 3,393 European ancestry individuals Illumina [~ 300000] 6 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001053 Genome-wide genotyping array 2011-05-28 21529783 Heath AC 2011-04-27 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21529783 A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications. Alcoholism (alcohol dependence factor score) 2,062 European ancestry alcohol dependence cases, 6,692 European ancestry controls 3,393 European ancestry individuals Illumina [~ 300000] 6 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001054 Genome-wide genotyping array 2009-01-14 19084217 Benyamin B 2008-12-17 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19084217 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. Iron status biomarkers 411 European ancestry individuals from 150 families NA Affymetrix [100846] 3 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST000302 Genome-wide genotyping array 2009-01-14 19084217 Benyamin B 2008-12-17 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19084217 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. Iron status biomarkers 459 European ancestry twin pairs NA Illumina [315887] 24 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST000301 Genome-wide genotyping array 2010-03-17 20147318 Qi L 2010-02-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20147318 Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes. E-selectin levels 501 European ancestry type 2 diabetes female cases, 504 European ancestry female controls 518 European ancestry female individuals Affymetrix [721316] 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST000606 Genome-wide genotyping array 2009-05-19 19430479 Levy D 2009-05-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19430479 Genome-wide association study of blood pressure and hypertension. Hypertension 29,136 European ancestry individuals 34,433 European ancestry individuals Affymetrix, Illumina [2533153] (imputed) 4 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST000398 Genome-wide genotyping array 2009-05-19 19430479 Levy D 2009-05-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19430479 Genome-wide association study of blood pressure and hypertension. Systolic blood pressure 29,136 European ancestry individuals 34,433 European ancestry individuals Affymetrix, Illumina [2533153] (imputed) 7 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST000393 Genome-wide genotyping array 2009-05-19 19430479 Levy D 2009-05-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19430479 Genome-wide association study of blood pressure and hypertension. Diastolic blood pressure 29,136 European ancestry individuals 34,433 European ancestry individuals Affymetrix, Illumina [2533153] (imputed) 7 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST000396 Genome-wide genotyping array 2011-01-16 21177295 Panoutsopoulou K 2010-12-21 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/21177295 Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study. Osteoarthritis 3,177 European ancestry cases, 4,894 European ancestry controls 10,312 European ancestry cases, 45,861 European ancestry controls, 213 cases, 2,531 controls Illumina [514898] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST000923 Genome-wide genotyping array 2010-10-06 20844546 Adachi S 2010-09-16 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20844546 Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population. Endometriosis 696 Japanese ancestry cases, 825 Japanese ancestry controls NA Affymetrix [282838] 2 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST000797 Genome-wide genotyping array 2010-02-12 20100581 Shen L 2010-01-22 Neuroimage www.ncbi.nlm.nih.gov/pubmed/20100581 Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. Brain imaging 175 European ancestry Alzheimer cases, 354 European ancestry amnestic mild cognitive impairment cases, 204 European ancestry controls NA Illumina [530992] 12 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST000573 Genome-wide genotyping array 2009-09-28 17911428 Cervino AC 2007-10-08 Ann N Y Acad Sci www.ncbi.nlm.nih.gov/pubmed/17911428 A genome-wide study of lupus: preliminary analysis and data release. Lupus 51 cases,114 controls NA Affymetrix [241701] 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000112 Genome-wide genotyping array 2008-07-22 18332876 Kirov G 2008-03-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/18332876 A genome-wide association study in 574 schizophrenia trios using DNA pooling. Schizophrenia 574 European ancestry trios, 605 European ancestry controls NA Illumina [~ 550000] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000163 Genome-wide genotyping array 2009-01-12 19079261 Willer CJ 2008-12-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19079261 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Body mass index 32,387 European ancestry individuals 59,082 European ancestry individuals Affymetrix, Illumina [2399588] (imputed) 11 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000298 Genome-wide genotyping array 2008-11-12 18849994 Hillmer AM 2008-10-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18849994 Susceptibility variants for male-pattern baldness on chromosome 20p11. Male-pattern baldness 296 European ancestry cases, 347 European ancestry controls 319 European ancestry cases, 234 European ancestry controls Illumina [531695] 1 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST000251 Genome-wide genotyping array 2009-03-31 19287384 Kilpivaara O 2009-03-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19287384 A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms. Myeloproliferative neoplasms 324 European ancestry cases, 2,999 European ancestry controls NA Affymetrix [62775] 1 myeloproliferative disorder http://www.ebi.ac.uk/efo/EFO_0004251 GCST000357 Genome-wide genotyping array 2010-09-22 20711177 Hamza TH 2010-08-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20711177 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Parkinson's disease 2,000 European ancestry cases, 1,986 European ancestry controls Up to 1,447 cases, 1,468 controls Illumina [811597] 4 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000772 Genome-wide genotyping array 2011-01-03 21072201 Kim JH 2010-11-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/21072201 Genome-wide and follow-up studies identify CEP68 gene variants associated with risk of aspirin-intolerant asthma. Aspirin intolerance in asthmatics 80 Korean ancestry cases, 100 Korean ancestry controls 163 Korean ancestry cases, 429 Korean ancestry controls Illumina [96984] 0 Aspirin-induced asthma http://purl.obolibrary.org/obo/HP_0012042 GCST000859 Genome-wide genotyping array 2010-01-19 20009918 Shrestha S 2010-01-01 AIDS www.ncbi.nlm.nih.gov/pubmed/20009918 A genome-wide association study of carotid atherosclerosis in HIV-infected men. Carotid atherosclerosis in HIV infection 177 European ancestry individuals NA Illumina [311194] 7 common carotid intimal medial thickness, internal carotid intimal medial thickness, carotid artery disease http://www.ebi.ac.uk/efo/EFO_0004860, http://www.ebi.ac.uk/efo/EFO_0005053, http://www.ebi.ac.uk/efo/EFO_0003781 GCST000555 Genome-wide genotyping array 2009-04-22 19343178 Soranzo N 2009-04-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19343178 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. Height 12,611 European ancestry individuals 7,187 European ancestry individuals Illumina [229216] 20 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000372 Genome-wide genotyping array 2015-04-22 21305692 Belmonte Mahon P 2011-02-08 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21305692 Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. Bipolar disorder (age of onset and psychotic symptoms) 2,836 European ancestry cases, 2,744 European ancestry controls 3,916 European cases, 5,112 controls Affymetrix, Illumina [2373895] (imputed) 2 psychotic symptoms, age of onset of bipolar disorder http://www.ebi.ac.uk/efo/EFO_0005940, http://purl.obolibrary.org/obo/OBA_2001019 GCST000969 Genome-wide genotyping array 2010-01-29 20062061 Chambers JC 2010-01-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20062061 Genetic variation in SCN10A influences cardiac conduction. Electrocardiographic traits 6,543 Indian Asian ancestry individuals 6,243 Indian Asian ancestry individuals, 5,370 European ancestry individuals Illumina [303309] 3 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST000564 Genome-wide genotyping array 2011-03-02 21273288 Del Greco M F 2011-01-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21273288 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. Natriuretic peptide levels 1,325 European ancestry individuals 1,746 European ancestry individuals Illumina [~ 2500000] (imputed) 3 NT-proBNP measurement http://www.ebi.ac.uk/efo/EFO_0004745 GCST000957 Genome-wide genotyping array 2009-03-03 19151714 Meyre D 2009-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19151714 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Obesity 695 European ancestry adult cases, 731 European ancestry adult controls, 685 European ancestry child cases, 685 European ancestry child controls 1,171 European ancestry adult cases, 1,114 European ancestry adult controls, 4,417 European ancestry adults, 896 European ancestry child cases, 1,297 European ancestry child and young adult controls, 5,291 European ancestry children Illumina [308846] 13 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST000317 Genome-wide genotyping array 2012-01-06 22144573 O'Donnell CJ 2011-12-05 Circulation www.ncbi.nlm.nih.gov/pubmed/22144573 Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Coronary artery calcification 9,961 European ancestry individuals 6,032 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 3 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST001347 Genome-wide genotyping array 2010-02-05 20070850 Edwards TL 2010-01-13 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/20070850 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. Parkinson's disease 1,752 European ancestry cases, 1,745 European ancestry controls NA Illumina [495715] (imputed) 6 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000567 Genome-wide genotyping array 2011-03-28 21270382 Baik I 2011-01-26 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/21270382 Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. Alcohol consumption 1,721 Korean ancestry male individuals 1,113 Korean ancestry male individuals Affymetrix [315914] 4 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST000954 Genome-wide genotyping array 2011-05-02 21460840 Hollingworth P 2011-04-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21460840 Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Alzheimer's disease 6,688 European ancestry cases, 13,685 European ancestry controls 13,182 European ancestry cases, 26,161 European ancestry controls Affymetrix, Illumina [496763] 4 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001025 Genome-wide genotyping array 2009-12-10 19915575 Simon-Sanchez J 2009-11-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19915575 Genome-wide association study reveals genetic risk underlying Parkinson's disease. Parkinson's disease 1,713 European ancestry cases, 3,978 European ancestry controls 3,361 European ancestry cases, 4,573 European ancestry controls Illumina [463185] 10 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000528 Genome-wide genotyping array 2013-09-27 23562540 Cruchaga C 2013-04-04 Neuron www.ncbi.nlm.nih.gov/pubmed/23562540 GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease. Alzheimer's disease biomarkers 591 European ancestry cases, 687 European ancestry controls Illumina [5815690] (imputed) 6 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001951 Genome-wide genotyping array 2010-06-23 20528957 Oedegaard KJ 2010-06-07 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/20528957 A genome-wide association study of bipolar disorder and comorbid migraine. Migraine in psychiatric disorder 56 European ancestry bipolar disorder cases, 699 European ancestry bipolar disorder controls 131 European ancestry attention deficit hyperactivity disorder cases, 324 European ancestry attention deficit hyperactivity disorder controls Affymetrix [724067] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST000695 Genome-wide genotyping array 2013-04-04 23328707 Tin A 2013-01-16 Nephrol Dial Transplant www.ncbi.nlm.nih.gov/pubmed/23328707 Genome-wide significant locus of beta-trace protein, a novel kidney function biomarker, identified in European and African Americans. Beta-trace protein levels 6,720 European ancestry individuals 1,734 African American individuals Affymetrix [~ 2500000] (imputed) 1 renal system measurement http://www.ebi.ac.uk/efo/EFO_0004742 GCST001825 Genome-wide genotyping array 2015-05-13 21347282 Lettre G 2011-02-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21347282 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Coronary heart disease 260 African American cases, 5,053 African American controls 621 African American cases, 1,629 African American controls Affymetrix [~ 2740000] (imputed) 3 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000972 Genome-wide genotyping array 2015-05-13 21347282 Lettre G 2011-02-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21347282 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Type 2 diabetes 1,264 African American cases, 5,678 African American controls 503 African American cases, 1,656 African American controls Affymetrix [~ 2740000] (imputed) 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000976 Genome-wide genotyping array 2015-05-13 21347282 Lettre G 2011-02-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21347282 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. LDL cholesterol 7,565 African American individuals 3,789 African American and Afro-Caribbean individuals Affymetrix [~ 2740000] (imputed) 17 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000975 Genome-wide genotyping array 2015-05-13 21347282 Lettre G 2011-02-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21347282 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. HDL cholesterol 7,813 African American individuals 4,323 African American and Afro-Caribbean individuals Affymetrix [~ 2740000] (imputed) 18 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000974 Genome-wide genotyping array 2015-05-13 21347282 Lettre G 2011-02-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21347282 Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project. Hypertension 4,069 African American cases, 3,848 African American controls 1,372 African American cases, 1,482 African American controls Affymetrix [~ 2740000] (imputed) 8 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST000973 Genome-wide genotyping array 2013-07-12 23565137 Miyashita A 2013-04-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/23565137 SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians. Alzheimer's disease (late onset) 891 Japanese ancestry cases, 844 Japanese ancestry controls 1,224 East Asian ancestry cases, 2,114 East Asian ancestry controls, 11,840 European ancestry cases, 10,931 European ancestry controls Affymetrix [5877918] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001947 Genome-wide genotyping array 2009-04-16 19349983 Kamatani Y 2009-04-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19349983 A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians. Hepatitis B 179 Japanese ancestry cases, 934 Japanese ancestry controls 1,599 Japanese ancestry cases, 2,821 Japanese ancestry controls, 308 Thai ancestry cases, 546 Thai ancestry controls Illumina [499544] 1 hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004197 GCST000375 Genome-wide genotyping array 2013-04-24 23354978 Rinella ES 2013-01-25 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23354978 Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation. Breast cancer 477 Ashkenazi Jewish cases, 524 Ashkenazi Jewish controls 203 Ashkenazi Jewish cases, 263 Ashkenazi Jewish contols Affymetrix [435632] 3 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001831 Genome-wide genotyping array 2009-10-15 19197348 Lowe JK 2009-02-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19197348 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. Quantitative traits 2,906 Kosraen individuals NA Affymetrix [408775] 33 waist circumference, total cholesterol measurement, body fat distribution, C-reactive protein measurement, body mass index, high density lipoprotein cholesterol measurement, body height, diastolic blood pressure, triglyceride measurement, systolic blood pressure, low density lipoprotein cholesterol measurement, body weight, thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004341, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0004339, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004748 GCST000337 Genome-wide genotyping array 2011-05-25 21505073 Terao C 2011-04-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21505073 The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. Rheumatoid arthritis 1,247 Japanese ancestry cases, 1,486 Japanese ancestry controls 4,168 Japanese ancestry cases, 5,003 Japanese ancestry controls Illumina [241523] 3 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST001042 Genome-wide genotyping array 2012-01-07 22137330 Sanchez-Juan P 2011-11-30 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22137330 Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk. Creutzfeldt-Jakob disease (variant) 93 European ancestry cases, 1,504 European ancestry controls 42 European ancestry cases Affymetrix [287554] 6 Creutzfeldt Jacob Disease http://www.ebi.ac.uk/efo/EFO_0004226 GCST001334 Genome-wide genotyping array 2008-06-16 17478679 Helgadottir A 2007-05-03 Science www.ncbi.nlm.nih.gov/pubmed/17478679 A common variant on chromosome 9p21 affects the risk of myocardial infarction. Myocardial infarction 1,607 European ancestry cases, 6,728 European ancestry controls 2,980 European ancestry cases, 6,309 European ancestry controls Illumina [305953] 1 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST000030 Genome-wide genotyping array 2010-09-23 20729853 Wang LD 2010-08-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20729853 Genome-wide association study of esophageal squamous cell carcinoma in Chinese subjects identifies susceptibility loci at PLCE1 and C20orf54. Esophageal cancer 1,077 Han Chinese ancestry cases, 1,733 Han Chinese ancestry controls 7,673 Han Chinese ancestry cases, 11,013 Han Chinese ancestry controls, 303 Uygur-Kazakh Chinese ancestry cases, 537 Uygur-Kazakh Chinese ancestry controls Illumina [506666] 0 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST000776 Genome-wide genotyping array 2009-09-30 19749757 Tanaka Y 2009-09-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19749757 Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. Response to hepatitis C treatment 64 Japanese ancestry responders, 78 Japanese ancestry non-responders 122 Japanese ancestry responders, 50 Japanese ancestry non-responders Affymetrix [621220] 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST000486 Genome-wide genotyping array 2010-03-23 20171287 Stein JL 2010-02-17 Neuroimage www.ncbi.nlm.nih.gov/pubmed/20171287 Voxelwise genome-wide association study (vGWAS). Brain structure 740 European ancestry individuals NA Illumina [448293] 19 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST000597 Genome-wide genotyping array 2009-08-21 19620980 Skibola CF 2009-07-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19620980 Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. Follicular lymphoma 189 European ancestry cases, 592 European controls 456 European ancestry cases, 2,785 European ancestry controls Illumina [~ 500000] 1 neoplasm of mature B-cells http://www.ebi.ac.uk/efo/EFO_0000096 GCST000448 Genome-wide genotyping array 2010-08-11 20601957 Uno S 2010-07-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20601957 A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. Endometriosis 1,423 Japanese ancestry cases, 1,318 Japanese ancestry controls 484 Japanese ancestry cases, 3,974 Japanese ancestry controls Illumina [460945] 2 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST000721 Genome-wide genotyping array 2012-01-28 22197932 Paternoster L 2011-12-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22197932 Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis. Atopic dermatitis 5,606 European ancestry cases, 20,565 European ancestry controls 5,419 European ancestry cases, 19,833 European ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 6 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST001363 Genome-wide genotyping array 2010-03-06 20169177 Yang W 2010-02-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20169177 Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus. Systemic lupus erythematosus 314 Chinese ancestry cases, 1,484 Chinese ancestry controls 2,630 Chinese ancestry cases, 2,155 Chinese ancestry controls, 314 Thai ancestry cases, 519 Thai ancestry controls Illumina [514221] 2 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000592 Genome-wide genotyping array 2009-05-07 18839057 Lesch KP 2008-10-07 J Neural Transm (Vienna) www.ncbi.nlm.nih.gov/pubmed/18839057 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. Attention deficit hyperactivity disorder 343 European ancestry cases, 250 European ancestry controls, 54 controls NA Affymetrix [504219] 26 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST000246 Genome-wide genotyping array 2009-11-18 19851299 Johansson A 2009-10-22 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/19851299 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. Weight Up to 3,925 European individuals NA Illumina [318237] 9 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST000511 Genome-wide genotyping array 2009-11-18 19851299 Johansson A 2009-10-22 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/19851299 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. Body mass index 1,079 South Tyrolean individuals, 790 Dutch founder individuals, 2,060 European ancestry individuals NA Illumina [318237] 10 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000512 Genome-wide genotyping array 2009-12-28 20183929 Nuinoon M 2009-11-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/20183929 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. Beta thalassemia/hemoglobin E disease 235 Thai-Chinese ancestry mild cases, 383 Thai-Chinese ancestry severe cases 52 Indonesian ancestry mild cases, 122 Indonesian ancestry severe cases Illumina [548094] 3 hemoglobin E disease http://purl.obolibrary.org/obo/MONDO_0016243 GCST000532 Genome-wide genotyping array 2008-09-17 18325910 Liu YJ 2008-03-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/18325910 Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. Obesity 1,000 European ancestry individuals 896 European ancestry cases, 2,916 European ancestry controls Affymetrix [379319] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST000159 Genome-wide genotyping array 2011-01-13 21160077 Gudmundsson J 2010-12-15 Sci Transl Med www.ncbi.nlm.nih.gov/pubmed/21160077 Genetic correction of PSA values using sequence variants associated with PSA levels. Serum prostate-specific antigen levels 7,538 European ancestry individuals 2,373 European ancestry individuals Illumina [304070] 7 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST000919 Genome-wide genotyping array 2009-12-01 19874204 Guo Y 2009-10-29 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/19874204 IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study. Bone mineral density 983 European ancestry individuals 2,557 European ancestry individuals from 750 families Affymetrix [342854] 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000515 Genome-wide genotyping array 2008-09-17 18327256 Doring A 2008-03-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18327256 SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. Urate levels 1,644 European ancestry individuals 9,947 European ancestry individuals Affymetrix [335152] 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST000161 Genome-wide genotyping array 2010-09-27 20802204 Baranzini SE 2010-09-01 Brain www.ncbi.nlm.nih.gov/pubmed/20802204 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. Multiple sclerosis--Brain Glutamate Levels 382 cases NA Illumina [~ 500000] 5 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000783 Genome-wide genotyping array 2009-05-05 19396169 Cho YS 2009-04-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19396169 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Height 8,842 Korean ancestry individuals 7,861 Korean ancestry individuals Affymetrix [2156535] (imputed) 5 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000380 Genome-wide genotyping array 2009-05-05 19396169 Cho YS 2009-04-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19396169 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. Biomedical quantitative traits 8,842 Korean ancestry individuals 7,861 Korean ancestry individuals Affymetrix [2156535] (imputed) 8 diastolic blood pressure, systolic blood pressure, bone density, heart rate, waist-hip ratio, body mass index http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0003923, http://www.ebi.ac.uk/efo/EFO_0004326, http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004340 GCST000381 Genome-wide genotyping array 2008-06-16 17634449 Samani NJ 2007-07-18 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/17634449 Genomewide association analysis of coronary artery disease. Coronary heart disease 1,926 European ancestry cases, 2,938 European ancestry controls 875 European ancestry cases, 1,644 European ancestry controls Affymetrix [377857] 7 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000057 Genome-wide genotyping array 2013-09-05 19744961 Hazra A 2009-09-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19744961 Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway. Folate pathway vitamin levels 3,305 European ancestry females, 1,458 European ancestry males NA Affymetrix, Illumina [~ 2500000] (imputed) 9 vitamin measurement http://www.ebi.ac.uk/efo/EFO_0004729 GCST000483 Genome-wide genotyping array 2011-01-06 21079607 Wang K 2010-11-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21079607 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. Anorexia nervosa 1,033 European ancestry cases, 3,733 European ancestry controls NA Illumina [~ 598000] 9 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST000873 Genome-wide genotyping array 2012-02-21 22295056 Christie JD 2012-01-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/22295056 Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major trauma. Acute lung injury 600 European ancestry cases, 2,266 European ancestry controls 212 European ancestry cases, 283 European ancestry controls Illumina [2487415] (imputed) 0 acute lung injury http://www.ebi.ac.uk/efo/EFO_0004610 GCST001383 Genome-wide genotyping array 2010-05-24 20418890 Tobacco and Genetics Consortium 2010-04-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20418890 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. Smoking behavior Up to 74,035 European ancestry individuals Up to 68,988 participants Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 5 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST000666 Genome-wide genotyping array 2009-12-29 20031603 Marroni F 2009-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031603 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. QT interval 2,325 European ancestry individuals NA Illumina [~ 318327] 14 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST000452 Genome-wide genotyping array 2009-12-29 20031603 Marroni F 2009-08-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031603 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. RR interval (heart rate) 2,325 European ancestry individuals NA Illumina [~ 318327] 20 RR interval http://www.ebi.ac.uk/efo/EFO_0004831 GCST000451 Genome-wide genotyping array 2009-09-04 19648919 Song H 2009-08-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19648919 A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. Ovarian cancer 1,817 European ancestry cases, 2,353 European ancestry controls 6,944 European ancestry cases, 9,477 European ancestry controls Illumina [up to 2000000] (imputed) 1 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST000455 Genome-wide genotyping array 2010-11-23 20932310 Han MR 2010-10-08 BMC Neurol www.ncbi.nlm.nih.gov/pubmed/20932310 Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study. Cerebrospinal T-tau levels 172 European ancestry Alzheimer's disease cases, 109 European ancestry mild cognitive impairment cases, 109 European ancestry controls NA Illumina [498205] 5 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST000826 Genome-wide genotyping array 2010-11-23 20932310 Han MR 2010-10-08 BMC Neurol www.ncbi.nlm.nih.gov/pubmed/20932310 Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study. Cerebrospinal P-tau181p levels 172 European ancestry Alzheimer's disease cases, 109 European ancestry mild cognitive impairment cases, 109 European ancestry controls NA Illumina [498205] 5 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST000825 Genome-wide genotyping array 2010-11-23 20932310 Han MR 2010-10-08 BMC Neurol www.ncbi.nlm.nih.gov/pubmed/20932310 Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study. Cerebrospinal fluid AB1-42 levels 172 European ancestry Alzheimer's disease cases, 109 European ancestry mild cognitive impairment cases, 109 European ancestry controls NA Illumina [498205] 7 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST000827 Genome-wide genotyping array 2009-05-07 19412176 Hallmayer J 2009-05-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19412176 Narcolepsy is strongly associated with the T-cell receptor alpha locus. Narcolepsy 807 European ancestry cases, 1,074 European ancestry controls 363 European ancestry cases, 355 European ancestry controls, 133 African American cases, 144 African American controls, 561 Asian ancestry cases, 605 Asian ancestry controls Affymetrix [549596] 1 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST000385 Genome-wide genotyping array 2009-12-28 20018961 Zhang FR 2009-12-16 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/20018961 Genomewide association study of leprosy. Leprosy 706 Han Chinese ancestry cases, 1,225 Han Chinese ancestry controls 3,254 Chinese ancestry cases, 5,955 Chinese ancestry controls Illumina [491883] 6 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST000546 Genome-wide genotyping array 2014-11-21 24795349 Saxena R 2014-05-03 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24795349 Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort. Telomere length 842 Punjabi Sikh ancestry type 2 diabetes cases, 774 Punjabi Sikh ancestry controls 1,108 Punjabi Sikh ancestry type 2 diabetes cases, 1,289 Punjabi Sikh ancestry controls, 2,952 European ancestry myocardial infarction cases and healthy controls, 10,033 European ancestry individuals Illumina [5904251] (imputed) 2 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST002437 Genome-wide genotyping array 2011-02-03 21211648 Ege MJ 2011-01-01 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/21211648 Gene-environment interaction for childhood asthma and exposure to farming in Central Europe. Asthma or atopy (farm exposure interaction) 850 European asthmatic child cases, 348 European atopic child cases, 510 European child controls NA Illumina [2500000] (imputed) 0 farm exposure measurement, asthma http://www.ebi.ac.uk/efo/EFO_0008362, http://purl.obolibrary.org/obo/MONDO_0004979 GCST000934 Genome-wide genotyping array 2013-11-15 23698163 Gong J 2013-05-21 Nutrients www.ncbi.nlm.nih.gov/pubmed/23698163 Genome-wide association study of serum selenium concentrations. Serum selenium levels 582 European ancestry individuals 621 European ancestry individuals Illumina [2474333] 4 serum selenium measurement http://www.ebi.ac.uk/efo/EFO_0005266 GCST002028 Genome-wide genotyping array 2009-12-03 19902172 Palmer ND 2009-11-10 Diabetologia www.ncbi.nlm.nih.gov/pubmed/19902172 Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Atherosclerosis (IRAS) Family Study. Insulin-related traits 229 Hispanic individuals from 34 families 814 Hispanic family members Illumina [309200] 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST000526 Genome-wide genotyping array 2009-04-01 19198611 Tregouet DA 2009-02-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19198611 Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Coronary heart disease 1,926 European ancestry cases, 2,938 European ancestry controls 7,073 European ancestry cases, 7,325 European ancestry controls Affymetrix [~ 500000] 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000341 Genome-wide genotyping array 2008-06-16 18204446 Harley JB 2008-01-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18204446 Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci. Systemic lupus erythematosus 720 European ancestry female cases, 2,337 European ancestry female controls 1,846 European ancestry female cases, 1,825 European ancestry female controls Illumina [317501] 6 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000142 Genome-wide genotyping array 2010-01-07 20011104 Richards JB 2009-12-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20011104 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. Adiponectin levels 8,531 European ancestry individuals 6,202 European ancestry individuals Affymetrix, Illumina [~ 2200000] (imputed) 3 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST000538 Genome-wide genotyping array 2010-03-29 20304703 Li Y 2010-03-19 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/20304703 Genetic variants and risk of lung cancer in never smokers: a genome-wide association study. Lung cancer 364 European ancestry cases, 364 European ancestry controls, 13 cases, 13 controls 446 European ancestry cases, 853 European ancestry controls, 65 cases, 154 controls Illumina [331918] 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000633 Genome-wide genotyping array 2010-03-22 20175129 Zhao LJ 2009-12-11 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/20175129 Genome-wide association study for femoral neck bone geometry. Femoral neck bone geometry 987 European ancestry individuals 1,488 European ancestry individuals, 2,118 Chinese ancestry individuals Affymetrix [379319] 0 femoral neck bone geometry http://www.ebi.ac.uk/efo/EFO_0004511 GCST000541 Genome-wide genotyping array 2008-09-12 17903304 Larson MG 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903304 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. Major CVD 142 cases and 1,203 controls from 310 families NA Affymetrix [70897] 1 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST000093 Genome-wide genotyping array 2008-10-14 17903304 Larson MG 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903304 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. Atrial fibrillation 151 cases and 1,190 controls from 310 families NA Affymetrix [70897] 3 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST000109 Genome-wide genotyping array 2009-09-28 17903304 Larson MG 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903304 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. Heart failure 75 cases and 1,272 controls from 310 families NA Affymetrix [70897] 1 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST000104 Genome-wide genotyping array 2008-09-25 18794855 Kiemeney LA 2008-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18794855 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. Urinary bladder cancer 1,803 European ancestry cases, 34,336 European ancestry controls 2,165 European ancestry cases, 3,800 European ancestry controls Illumina [302140] 2 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST000231 Genome-wide genotyping array 2009-11-04 19798445 Hicks AA 2009-10-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19798445 Genetic determinants of circulating sphingolipid concentrations in European populations. Sphingolipid levels 4,110 European ancestry individuals NA Illumina [318237] 5 sphingolipid measurement http://www.ebi.ac.uk/efo/EFO_0004622 GCST000493 Genome-wide genotyping array 2011-02-22 21216879 Kaplan RC 2011-01-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21216879 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. Insulin-like growth factors 10,280 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 IGFBP-3 measurement http://www.ebi.ac.uk/efo/EFO_0004626 GCST000937 Genome-wide genotyping array 2010-05-23 20418485 Ahn J 2010-04-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20418485 Genome-wide association study of circulating vitamin D levels. Vitamin D levels 4,501 European ancestry individuals 2,221 European ancestry individuals Affymetrix, Illumina [593253] (imputed) 3 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST000664 Genome-wide genotyping array 2010-07-04 20548944 Hsu YH 2010-06-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20548944 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. Osteoporosis-related phenotypes 2,038 European ancestry female individuals, 1,531 European ancestry male individuals 5,595 European ancestry female individuals, 2,126 European ancestry male individuals Affymetrix [433510] 7 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST000698 Genome-wide genotyping array 2011-11-24 22019778 Zhang F 2011-10-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22019778 Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy. Leprosy 706 Han Chinese ancestry cases, 5,581 Han Chinese ancestry controls 3,301 Han Chinese ancestry cases, 5,299 Han Chinese ancestry controls NR [1701673] (imputed) 4 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST001292 Genome-wide genotyping array 2011-04-13 21441570 Grassi MA 2011-03-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21441570 Genome-wide meta-analysis for severe diabetic retinopathy. Diabetic retinopathy 973 European ancestry cases, 1,856 European ancestry controls NA Affymetrix, Illumina [2543887] (imputed) 19 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST001017 Genome-wide genotyping array 2011-04-13 21423239 Willour VL 2011-03-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21423239 A genome-wide association study of attempted suicide. Suicide attempts in bipolar disorder 1,201 European and unknown ancestry attempters, 1,497 European and unknown ancestry non-attempters 1,295 attempters, 1,822 non-attempters Affymetrix, Illumina [2408051] (imputed) 3 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST001015 Genome-wide genotyping array 2009-12-29 20031582 Thompson JF 2009-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031582 Comprehensive whole-genome and candidate gene analysis for response to statin therapy in the Treating to New Targets (TNT) cohort. Response to statin therapy 1,984 European ancestry individuals 3,761 European ancestry individuals, 1,248 individuals Perlegen [291998] 0 response to statin http://purl.obolibrary.org/obo/GO_0036273 GCST000369 Genome-wide genotyping array 2010-06-21 20516156 Lewis CM 2010-06-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/20516156 Genome-wide association study of major recurrent depression in the U.K. population. Major depressive disorder 1,636 European ancestry cases, 1,594 European ancestry controls 1,418 European ancestry cases, 1,918 European ancestry controls Illumina [471747] 4 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST000689 Genome-wide genotyping array 2010-09-11 20670164 Horinouchi M 2010-08-01 Pediatr Hematol Oncol www.ncbi.nlm.nih.gov/pubmed/20670164 Association of genetic polymorphisms with hepatotoxicity in patients with childhood acute lymphoblastic leukemia or lymphoma. Acute lymphoblastic leukemia (childhood) 8 Japanese ancestry cases 16 Japanese ancestry cases Illumina [~ 318000] 0 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST000749 Genome-wide genotyping array 2011-01-03 21184583 Zlojutro M 2010-11-02 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21184583 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. Event-related brain oscillations 431 European ancestry alcohol dependence cases, 340 European ancestry controls, 209 African American alcohol dependence cases, 84 African American controls 683 alcohol dependence cases and 412 controls from multiplex families Illumina [951071] 3 event-related brain oscillation http://www.ebi.ac.uk/efo/EFO_0004358 GCST000857 Genome-wide genotyping array 2012-02-25 22290723 Ryu J 2012-01-30 Hum Mutat www.ncbi.nlm.nih.gov/pubmed/22290723 Association of glycosylated hemoglobin with the gene encoding CDKAL1 in the Korean Association Resource (KARE) study. Glycated hemoglobin levels 4,275 Korean ancestry individuals 3,782 Korean ancestry individuals Affymetrix [1693116] (imputed) 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST001393 Genome-wide genotyping array 2011-01-14 21130836 Luciano M 2010-12-03 Biol Psychol www.ncbi.nlm.nih.gov/pubmed/21130836 Whole genome association scan for genetic polymorphisms influencing information processing speed. Information processing speed Up to 4,039 European ancestry individuals NA Illumina [~ 610000] 25 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST000905 Genome-wide genotyping array 2013-10-24 23563609 Wheeler E 2013-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23563609 Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. Obesity (early onset extreme) 1,509 European ancestry cases, 5,380 European ancestry controls 971 European ancestry cases, 1,990 European ancestry controls Affymetrix [~ 2000000] (imputed) 18 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001957 Genome-wide genotyping array 2009-12-28 20023658 Mangold E 2009-12-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20023658 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Orofacial clefts 399 European ancestry cases, 1,318 European ancestry controls 655 European ancestry triads Illumina [521288] 6 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST000547 Genome-wide genotyping array 2011-05-11 21483023 Wu X 2011-04-11 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/21483023 Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy. Response to platinum-based chemotherapy in non-small-cell lung cancer 327 European ancestry individuals 735 European ancestry individuals Illumina [307260] 1 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST001035 Genome-wide genotyping array 2011-04-11 21378990 Schunkert H 2011-03-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21378990 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Coronary heart disease 22,233 European ancestry cases, 64,762 European ancestry controls 56,682 European ancestry cases and controls Affymetrix, Illumina [~ 2300000] (imputed) 30 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000998 Genome-wide genotyping array 2010-11-15 20932654 Kerns SL 2010-10-05 Int J Radiat Oncol Biol Phys www.ncbi.nlm.nih.gov/pubmed/20932654 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. Erectile dysfunction and prostate cancer treatment 27 African American cases, 52 African American controls NA Affymetrix [512497] 23 response to radiation, prostate carcinoma, erectile dysfunction http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0001663, http://www.ebi.ac.uk/efo/EFO_0004234 GCST000824 Genome-wide genotyping array 2011-02-23 21228123 Ochi H 2011-01-12 J Gen Virol www.ncbi.nlm.nih.gov/pubmed/21228123 IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations. Response to hepatitis C treatment 2,101 East Asian ancestry cases, 282 Japanese ancestry controls NA Illumina [510537] 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST000944 Genome-wide genotyping array 2009-05-12 19414484 Johnson AD 2009-05-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19414484 Genome-wide association meta-analysis for total serum bilirubin levels. Bilirubin levels 9,464 individuals NA Affymetrix, Illumina [2555103] (imputed) 8 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST000386 Genome-wide genotyping array 2012-01-11 22130093 Nam RK 2011-12-01 Cancer Biol Ther www.ncbi.nlm.nih.gov/pubmed/22130093 New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort. Prostate cancer 316 cases, 229 controls 55 Asian ancestry cases, 134 Asian ancestry controls, 1,382 European ancestry cases, 1,428 European ancestry controls, 184 Black cases, 127 Black controls, 42 cases, 87 controls Affymetrix [443816] 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001338 Genome-wide genotyping array 2011-01-13 21051598 Pereyra F 2010-11-04 Science www.ncbi.nlm.nih.gov/pubmed/21051598 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. HIV-1 control 516 European cases, 1,196 European controls, 341 African American cases, 892 African American controls, 117 Hispanic cases, 560 Hispanic controls NA Illumina [1384048] (imputed) 8 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST000863 Genome-wide genotyping array 2009-05-11 19403135 Yamada Y 2009-04-05 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/19403135 Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. Stroke (ischemic) 131 Japanese ancestry cases, 135 Japanese ancestry controls 776 Japanese ancestry cases, 5,205 Japanese ancestry controls Affymetrix [~ 520000] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST000373 Genome-wide genotyping array 2010-03-15 20167578 Barbalic M 2010-02-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20167578 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. Soluble levels of adhesion molecules Up to 9,813 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 5 adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0004522 GCST000599 Genome-wide genotyping array 2010-06-22 20526339 Quan C 2010-06-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20526339 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. Vitiligo 1,117 Han Chinese ancestry cases, 1,429 Han Chinese ancestry controls 6,623 East Asian ancestry cases, 10,740 East Asian ancestry controls Illumina [493909] 4 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST000692 Genome-wide genotyping array 2009-06-22 19096518 Pare G 2008-12-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19096518 Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study. Glycated hemoglobin levels 14,618 European ancestry females 455 European ancestry individuals Illumina [337343] 4 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST000303 Genome-wide genotyping array 2009-03-31 19260141 Zemunik T 2009-02-01 Croat Med J www.ncbi.nlm.nih.gov/pubmed/19260141 Genome-wide association study of biochemical traits in Korcula Island, Croatia. Biochemical measures 898 Korculan (founder/genetic isolate) individuals NA Illumina [316730] 17 serum albumin measurement, total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, fibrinogen measurement, uric acid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004535, http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0004761, http://www.ebi.ac.uk/efo/EFO_0004612 GCST000328 Genome-wide genotyping array 2010-09-16 20694014 Thye T 2010-08-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20694014 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. Tuberculosis 2,237 Sub-Saharan African ancestry cases, 3,122 Sub-Saharan African ancestry controls 1,462 Sub-Saharan African ancestry cases, 4,604 Sub-Saharan African ancestry controls Affymetrix [> 333754] (imputed) 14 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST000764 Genome-wide genotyping array 2009-01-21 19118814 Beecham GW 2009-01-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19118814 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. Alzheimer's disease 492 European ancestry cases, 496 European ancestry controls 238 European ancestry cases, 220 European ancestry controls Illumina [~ 2500000] (imputed) 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000310 Genome-wide genotyping array 2011-06-25 21654844 Briggs FB 2011-06-09 Genes Immun www.ncbi.nlm.nih.gov/pubmed/21654844 Genome-wide association study of severity in multiple sclerosis. Multiple sclerosis 1,470 European ancestry cases NA Affymetrix [2110417] (imputed) 6 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST001096 Genome-wide genotyping array 2010-07-12 20581827 Voight BF 2010-06-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20581827 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Type 2 diabetes 8,130 European ancestry cases, 38,987 European ancestry controls Up to 34,412 European ancestry cases, 59,925 European ancestry controls Affymetrix, Illumina [2426886] (imputed) 26 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000712 Genome-wide genotyping array 2011-02-22 21212386 Arnett DK 2011-01-06 Circ Res www.ncbi.nlm.nih.gov/pubmed/21212386 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. Cardiac muscle measurement 1,258 Black individuals 989 Black individuals, 1,316 European ancestry individuals Affymetrix [872242] 3 cardiovascular measurement, left ventricular hypertrophy http://www.ebi.ac.uk/efo/EFO_0004298, http://www.ebi.ac.uk/efo/EFO_0003896 GCST000936 Genome-wide genotyping array 2010-09-15 20700443 Meyer TE 2010-08-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20700443 Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels. Magnesium levels 15,366 European ancestry individuals 8,463 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 9 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST000756 Genome-wide genotyping array 2009-07-24 19578179 Teichert M 2009-07-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19578179 A genome-wide association study of acenocoumarol maintenance dosage. Acenocoumarol maintenance dosage 1,451 European ancestry individuals 287 individuals Illumina [~ 550000] 4 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST000436 Genome-wide genotyping array 2012-10-19 21102463 Franke A 2010-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21102463 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Crohn's disease 6,333 European ancestry cases, 15,056 European ancestry controls 15,694 European ancestry cases, 14,026 European ancestry controls, 414 European ancestry trios Affymetrix, Illumina [953241] (imputed) 71 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000879 Genome-wide genotyping array 2010-12-09 20972440 Houlston RS 2010-10-24 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20972440 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33. Colorectal cancer 3,334 European ancestry cases, 4,628 European ancestry controls 14,851 European ancestry cases, 15,569 European ancestry controls Illumina [up to 550000] (imputed) 5 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000843 Genome-wide genotyping array 2011-01-15 21197116 Ryu E 2010-12-17 Mol Vis www.ncbi.nlm.nih.gov/pubmed/21197116 Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study. Age-related macular degeneration 576 European ancestry individuals, 12 Black individuals, 2 individuals 444 European ancestry and Hispanic cases, 300 European ancestry and Hispanic controls Illumina [103895] 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST000921 Genome-wide genotyping array 2011-01-03 21037115 Wan ES 2010-10-29 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/21037115 Genome-wide association analysis of body mass in chronic obstructive pulmonary disease. Body mass in chronic obstructive pulmonary disease 2,950 European ancestry cases 502 European ancestry cases Illumina [~ 550000] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000850 Genome-wide genotyping array 2011-03-04 21223598 Wineinger NE 2011-01-11 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/21223598 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. Aortic root size 1,086 African American individuals NA Affymetrix [NR] 7 aortic root size http://www.ebi.ac.uk/efo/EFO_0005037 GCST000943 Genome-wide genotyping array 2010-05-03 20383147 Radstake TR 2010-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20383147 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. Systemic sclerosis 2,296 European ancestry cases, 5,171 European ancestry controls 2,753 European ancestry cases, 4,569 European ancestry controls Illumina [279621] 4 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST000650 Genome-wide genotyping array 2009-07-10 19571808 Stefansson H 2009-07-01 Nature www.ncbi.nlm.nih.gov/pubmed/19571808 Common variants conferring risk of schizophrenia. Schizophrenia 2,663 European ancestry cases, 13,498 European ancestry controls 10,282 European ancestry cases, 21,093 European ancestry controls Illumina [314868] 7 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000435 Genome-wide genotyping array 2011-01-19 21160409 Petrovski S 2010-12-14 AIDS www.ncbi.nlm.nih.gov/pubmed/21160409 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. HIV-1 susceptibility 531 Sub-Saharan African ancestry cases, 848 Sub-Saharan African ancestry controls NA Illumina [~ 800000] 6 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST000918 Genome-wide genotyping array 2009-02-27 19136949 Carrasquillo MM 2009-01-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19136949 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. Alzheimer's disease 844 European ancestry cases, 1,255 European ancestry controls 1,547 European ancestry cases, 1,209 European ancestry controls Illumina [313504] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000315 Genome-wide genotyping array 2009-06-01 19448189 Perlis RH 2009-05-15 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/19448189 A genomewide association study of response to lithium for prevention of recurrence in bipolar disorder. Response to lithium treatment in bipolar disorder 458 lithium-treated cases, 719 non-lithium treated cases 359 European ancestry lithium-treated cases Affymetrix [~ 1400000] (imputed) 0 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST000402 Genome-wide genotyping array 2008-07-01 18391951 Gudbjartsson DF 2008-04-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18391951 Many sequence variants affecting diversity of adult human height. Height 30,968 European ancestry individuals 8,541 European ancestry individuals Affymetrix, Illumina [up to 304226] 52 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000175 Genome-wide genotyping array 2009-03-18 19252134 Pezzolesi MG 2009-02-27 Diabetes www.ncbi.nlm.nih.gov/pubmed/19252134 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes. Type 2 diabetes nephropathy 820 European ancestry cases, 885 European ancestry controls 1,304 European ancestry individuals Affymetrix [359193] 0 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST000348 Genome-wide genotyping array 2008-09-16 18385739 Thorgeirsson TE 2008-04-03 Nature www.ncbi.nlm.nih.gov/pubmed/18385739 A variant associated with nicotine dependence, lung cancer and peripheral arterial disease. Nicotine dependence 10,995 European ancestry individuals 4,848 European ancestry individuals Illumina [306207] 1 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST000171 Genome-wide genotyping array 2009-01-16 19079262 Styrkarsdottir U 2008-12-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19079262 New sequence variants associated with bone mineral density. Bone mineral density (hip) 6,865 European ancestry individuals 8,510 European ancestry individuals Illumina [305051] 8 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000297 Genome-wide genotyping array 2009-01-16 19079262 Styrkarsdottir U 2008-12-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19079262 New sequence variants associated with bone mineral density. Bone mineral density (spine) 6,865 European ancestry individuals 8,510 European ancestry individuals Illumina [305051] 7 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000295 Genome-wide genotyping array 2009-09-28 17903307 Wilk JB 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903307 Framingham Heart Study genome-wide association: results for pulmonary function measures. Mean forced vital capacity from 2 exams Up to 1,222 individuals NA Affymetrix [70897] 2 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST000099 Genome-wide genotyping array 2008-09-10 17903307 Wilk JB 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903307 Framingham Heart Study genome-wide association: results for pulmonary function measures. Pulmonary function Up to 1,222 individuals NA Affymetrix [70897] 10 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST000106 Genome-wide genotyping array 2008-06-16 18369459 Liu Y 2008-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/18369459 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. Psoriasis 218 European ancestry cases, 519 European ancestry controls 1,153 European ancestry cases, 1,217 European ancestry controls Illumina [305983] 3 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST000173 Genome-wide genotyping array 2013-08-20 20848476 Haritunians T 2010-11-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/20848476 Genetic predictors of medically refractory ulcerative colitis. Ulcerative colitis 324 European ancestry medically refractory ulcerative colitis cases, 537 European ancestry non-medically refractory ulcerative colitis cases, 2,601 European ancestry controls NA Illumina [313720] 10 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000853 Genome-wide genotyping array 2008-09-12 18391950 Lettre G 2008-04-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18391950 Identification of ten loci associated with height highlights new biological pathways in human growth. Height 15,821 European ancestry individuals Up to 17,801 European ancestry individuals Affymetrix, Illumina [2260683] (imputed) 18 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000176 Genome-wide genotyping array 2009-07-13 19578365 Falchi M 2009-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19578365 Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. Cutaneous nevi 1,524 European ancestry twins 4,107 European ancestry individuals, 3,131 European ancestry cases, 4,276 European ancestry controls Illumina [297108] 2 nevus http://www.ebi.ac.uk/efo/EFO_0000625 GCST000438 Genome-wide genotyping array 2009-07-01 19557161 Lindgren CM 2009-06-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19557161 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. Adiposity 38,580 European ancestry individuals Up to 102,064 European ancestry individuals Affymetrix, Illumina [2573738] (imputed) 4 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST000428 Genome-wide genotyping array 2009-07-12 19578367 Shete S 2009-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19578367 Genome-wide association study identifies five susceptibility loci for glioma. Glioma 1,878 European ancestry cases, 3,670 European ancestry controls 2,545 European ancestry cases, 2,953 European ancestry controls Illumina [454576] 7 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST000439 Genome-wide genotyping array 2008-06-16 18204098 Hom G 2008-01-20 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/18204098 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. Systemic lupus erythematosus 1,311 European ancestry cases, 3,340 European ancestry controls 793 European ancestry cases, 857 European ancestry controls Illumina [502033] 9 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000144 Genome-wide genotyping array 2010-03-12 20200953 Karasik D 2010-01-29 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/20200953 Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study. Osteoporosis-related phenotypes 2,073 related female individuals NA Affymetrix [433510] 1 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST000575 Genome-wide genotyping array 2009-12-14 19915573 Asano K 2009-11-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19915573 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. Ulcerative colitis 376 Japanese ancestry cases, 934 Japanese ancestry controls 376 Japanese ancestry cases, 1,097 Japanese ancestry controls Illumina [513923] 7 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000529 Genome-wide genotyping array 2009-09-29 19734902 Harold D 2009-09-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19734902 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. Alzheimer's disease 3,941 European ancestry cases, 7,848 European ancestry controls 2,023 European ancestry cases, 2,340 European ancestry controls Illumina [529205] 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000479 Genome-wide genotyping array 2009-07-16 19578364 Bishop DT 2009-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19578364 Genome-wide association study identifies three loci associated with melanoma risk. Melanoma 1,539 European ancestry cases, 3,917 European ancestry controls 2,312 European ancestry cases, 1,867 European ancestry controls Illumina [~ 317000] 5 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST000437 Genome-wide genotyping array 2008-06-16 17529974 Stacey SN 2007-05-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17529974 Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. Breast cancer 1,599 European ancestry cases, 11,546 European ancestry controls 2,954 European ancestry cases, 5,967 European ancestry controls, Up to 561 Japanese ancestry cases, Up to 565 Japanese ancestry control, Up to 422 African American cases, Up to 448 African American controls, Up to 418 Hispanic cases, Up to 422 Hispanic controls, Up to 148 cases, Up to 293 controls Illumina [311524] 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000037 Genome-wide genotyping array 2013-03-27 23359319 Jin G 2013-01-01 Neoplasia www.ncbi.nlm.nih.gov/pubmed/23359319 Genome-wide association study identifies loci at ATF7IP and KLK2 associated with percentage of circulating free PSA. Prostate-specific antigen levels 3,192 European ancestry individuals 1,722 European ancestry individuals Illumina [642584] 2 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST001799 Genome-wide genotyping array 2008-09-10 17903301 Vasan RS 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903301 Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study. Exercise treadmill test traits Up to 1,238 European ancestry individuals NA Affymetrix [70897] 4 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST000089 Genome-wide genotyping array 2008-09-10 17903301 Vasan RS 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903301 Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study. Echocardiographic traits Up to 1,238 European ancestry individuals NA Affymetrix [70897] 8 cardiovascular measurement, left ventricular function, left atrial function http://www.ebi.ac.uk/efo/EFO_0004298, http://www.ebi.ac.uk/efo/EFO_0004295, http://www.ebi.ac.uk/efo/EFO_0004294 GCST000110 Genome-wide genotyping array 2008-09-17 17903301 Vasan RS 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903301 Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study. Endothelial function traits Up to 1,238 European ancestry individuals NA Affymetrix [70897] 1 cardiovascular measurement http://www.ebi.ac.uk/efo/EFO_0004298 GCST000102 Genome-wide genotyping array 2010-09-10 20668430 Genovese G 2010-07-28 Kidney Int www.ncbi.nlm.nih.gov/pubmed/20668430 A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. Glomerulosclerosis 56 African American cases, 61 European ancestry cases, 1,759 African American controls, 1,531 European ancestry controls 299 European ancestry cases Illumina [up to 542539] 1 focal segmental glomerulosclerosis http://www.ebi.ac.uk/efo/EFO_0004236 GCST000741 Genome-wide genotyping array 2008-10-14 18729187 Galvan A 2008-08-26 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/18729187 A polygenic model with common variants may predict lung adenocarcinoma risk in humans. Lung adenocarcinoma 482 European ancestry cases, 522 European ancestry controls NA Illumina [~ 318000] 0 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST000223 Genome-wide genotyping array 2008-10-14 18759275 McArdle PF 2008-09-01 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/18759275 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. Uric acid levels 408 Old Order Amish female individuals, 460 Old Order Amish male individuals Framingham Heart Study (Sample size NR) Affymetrix [361034] 7 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST000227 Genome-wide genotyping array 2013-10-31 20558996 Ott J 2010-06-17 Hum Hered www.ncbi.nlm.nih.gov/pubmed/20558996 Pilot study on schizophrenia in Sardinia. Schizophrenia 14 Sardinian cases, 23 Sardinian controls NA Affymetrix [255053] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000702 Genome-wide genotyping array 2008-06-16 17554261 Parkes M 2007-06-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17554261 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. Crohn's disease 1,748 cases, 2,938 controls 1,182 European ancestry cases, 2,024 European ancestry controls Affymetrix [see WTCCC] 9 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000039 Genome-wide genotyping array 2009-07-12 19578366 Wrensch M 2009-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19578366 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. Glioma (high-grade) 692 European ancestry cases, 3,992 European ancestry controls 176 cases, 174 controls Illumina [326506] 3 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST000440 Genome-wide genotyping array 2013-08-24 23571587 Reitz C 2013-04-10 JAMA www.ncbi.nlm.nih.gov/pubmed/23571587 Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans. Alzheimer's disease (late onset) 1,968 African American cases, 3,928 African American controls Illumina [17332474] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001963 Genome-wide genotyping array 2009-12-04 19896111 Medland SE 2009-11-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19896111 Common variants in the trichohyalin gene are associated with straight hair in Europeans. Hair morphology 4,845 European ancestry individuals from 2,892 families, 16,140 European ancestry individuals NA Illumina [~ 1000000] (imputed) 15 hair morphology http://www.ebi.ac.uk/efo/EFO_0005038 GCST000519 Genome-wide genotyping array 2008-11-12 18823527 Abraham R 2008-09-29 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/18823527 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. Alzheimer's disease 1,082 European ancestry cases, 1,239 European ancestry controls 1,400 controls Illumina [561494] 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000237 Genome-wide genotyping array 2011-05-11 21473668 Fliers EA 2011-04-07 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21473668 Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function. Attention deficit hyperactivity disorder motor coordination 890 European ancestry children 296 European ancestry children Perlegen [384401] 1 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST001030 Genome-wide genotyping array 2008-11-11 18840781 Grant SF 2008-10-07 Diabetes www.ncbi.nlm.nih.gov/pubmed/18840781 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. Type 1 diabetes 563 European ancestry cases, 1,146 European ancestry controls, 483 European ancestry trios 3,303 European ancestry cases, 4,673 European ancestry controls Illumina [up to 1000000] 5 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000244 Genome-wide genotyping array 2009-09-28 17903292 Hwang SJ 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903292 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. Cystatin C levels 981 individuals NA Affymetrix [70897] 1 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST000091 Genome-wide genotyping array 2008-09-02 17903292 Hwang SJ 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903292 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. Thyroid stimulating hormone levels 883 individuals NA Affymetrix [70897] 3 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST000100 Genome-wide genotyping array 2008-09-11 17903292 Hwang SJ 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903292 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. Urinary albumin excretion 822 individuals NA Affymetrix [70897] 2 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST000105 Genome-wide genotyping array 2013-04-18 23337944 Haghighi A 2013-01-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23337944 Opioid receptor mu 1 gene, fat intake and obesity in adolescence. Fat intake 598 European ancestry adolescents 490 European ancestry young adult individuals Illumina [530011] 0 energy intake http://www.ebi.ac.uk/efo/EFO_0003939 GCST001829 Genome-wide genotyping array 2008-06-16 17553421 Reiman EM 2007-06-07 Neuron www.ncbi.nlm.nih.gov/pubmed/17553421 GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. Alzheimer's disease (late onset) 446 cases, 290 controls 415 cases, 260 controls Affymetrix [312316] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000046 Genome-wide genotyping array 2009-01-14 19074352 Pollin TI 2008-12-17 Science www.ncbi.nlm.nih.gov/pubmed/19074352 A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. Triglycerides 809 Old Order Amish individuals 698 Old Order Amish individuals Affymetrix [381934] 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000300 Genome-wide genotyping array 2008-06-16 17463249 Zeggini E 2007-04-26 Science www.ncbi.nlm.nih.gov/pubmed/17463249 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. Type 2 diabetes 1,924 European ancestry cases, 2,938 European ancestry controls 3,757 European ancestry cases, 5,346 European ancestry controls Affymetrix [393453] 10 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000025 Genome-wide genotyping array 2009-05-11 19404256 Wang K 2009-04-28 Nature www.ncbi.nlm.nih.gov/pubmed/19404256 Common genetic variants on 5p14.1 associate with autism spectrum disorders. Autism 3,101 European ancestry individuals from 780 families, 1,204 European ancestry cases, 6,491 European ancestry controls 1,390 European ancestry individuals from 447 families, 108 European ancestry cases, 540 European ancestry controls Illumina [474019] 1 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST000382 Genome-wide genotyping array 2009-12-29 20031579 Tarasov KV 2009-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031579 COL4A1 is associated with arterial stiffness by genome-wide association scan. Arterial stiffness 4,221 Sardinian individuals 1,828 Sardinian individuals, 813 Old Order Amish individuals Affymetrix [362129] (imputed) 1 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST000370 Genome-wide genotyping array 2008-10-14 18463975 Kibriya MG 2008-05-08 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/18463975 A pilot genome-wide association study of early-onset breast cancer. Breast cancer 26 European ancestry cases, 3 Hispanic cases, 1 African American case, 26 European ancestry controls, 3 Hispanic controls, 1 African American control NA Affymetrix [200220] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000187 Genome-wide genotyping array 2009-04-03 18711367 Yasuda K 2008-08-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18711367 Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. Type 2 diabetes 187 Japanese ancestry cases, 1,504 Japanese ancestry controls 6,552 East Asian ancestry cases, 6,621 East Asian ancestry controls, 2,830 European ancestry cases, 3,740 European ancestry controls NR [82343] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000219 Genome-wide genotyping array 2008-06-16 17554260 Todd JA 2007-06-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17554260 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. Type 1 diabetes 2,000 European ancestry cases, 3,000 European ancestry controls 2,997 European ancestry trios, 4,000 European ancestry cases, 5,000 European ancestry controls Affymetrix [NR] 12 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000038 Genome-wide genotyping array 2009-04-02 19304780 Org E 2009-03-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19304780 Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. Hypertension 364 European ancestry cases, 590 European ancestry controls 1,043 European ancestry cases, 1,769 European ancestry controls Affymetrix [395912] 1 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST000361 Genome-wide genotyping array 2008-10-14 18776929 Liu YZ 2008-09-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/18776929 Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study. Hip bone size 501 European ancestry female individuals, 499 European ancestry male individuals 1,216 European ancestry female individuals Affymetrix [306823] 1 hip bone size http://www.ebi.ac.uk/efo/EFO_0004844 GCST000229 Genome-wide genotyping array 2013-09-21 23678272 Cheong KA 2013-05-02 J Korean Med Sci www.ncbi.nlm.nih.gov/pubmed/23678272 Three new single nucleotide polymorphisms identified by a genome-wide association study in Korean patients with vitiligo. Vitiligo (non-segmental) 20 Korean ancestry cases, 192 Korean ancestry controls 184 Korean ancestry cases, 192 Korean ancestry controls Affymetrix [500568] 1 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST001992 Genome-wide genotyping array 2015-05-23 24556642 Zeng Z 2014-02-18 Caries Res www.ncbi.nlm.nih.gov/pubmed/24556642 Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries. Pit-and-Fissure caries 979 European ancestry individuals NA Illumina [1216074] (imputed) 14 pit and fissure surface dental caries http://www.ebi.ac.uk/efo/EFO_0006338 GCST002358 Genome-wide genotyping array 2014-10-21 24556642 Zeng Z 2014-02-18 Caries Res www.ncbi.nlm.nih.gov/pubmed/24556642 Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries. Smooth-surface caries 1006 European ancestry individuals NA Illumina [1216189] (imputed) 31 smooth surface dental caries http://www.ebi.ac.uk/efo/EFO_0006339 GCST002361 Genome-wide genotyping array 2009-09-24 19714249 Liu YZ 2009-08-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/19714249 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. Obesity and osteoporosis 499 European ancestry male individuals, 501 European ancestry female individuals 1,370 European ancestry male individuals and 1,985 European ancestry female individuals from 975 families Affymetrix [379319] 2 obesity, osteoporosis http://www.ebi.ac.uk/efo/EFO_0001073, http://www.ebi.ac.uk/efo/EFO_0003882 GCST000469 Genome-wide genotyping array 2012-01-20 22210626 Mead S 2011-12-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22210626 Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Prion diseases 1,281 European ancestry cases, 6,015 European ancestry controls, 290 Papua New Guinean ancestry cases, 286 Papua New Guinean ancestry controls NA Illumina [NR] (imputed) 11 prion disease http://www.ebi.ac.uk/efo/EFO_0004720 GCST001366 Genome-wide genotyping array 2013-04-30 21519539 Cho SC 2011-02-25 Psychiatry Investig www.ncbi.nlm.nih.gov/pubmed/21519539 Genome-wide association scan of korean autism spectrum disorders with language delay: a preliminary study. Autism spectrum disorders (language delay) 42 Korean ancestry male cases and their parental controls NA Affymetrix [331095] 0 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST000991 Genome-wide genotyping array 2008-09-15 17641165 Fellay J 2007-07-19 Science www.ncbi.nlm.nih.gov/pubmed/17641165 A whole-genome association study of major determinants for host control of HIV-1. HIV-1 viral setpoint 486 European ancestry cases 140 European ancestry cases Illumina [535101] 0 response to virus http://purl.obolibrary.org/obo/GO_0009615 GCST000059 Genome-wide genotyping array 2010-03-24 20228798 Franke A 2010-03-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20228798 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). Ulcerative colitis 1,043 European ancestry cases, 1,703 European ancestry controls 2,539 European ancestry cases, 5,428 European ancestry controls Affymetrix [1897764] (imputed) 6 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000623 Genome-wide genotyping array 2008-06-16 17632545 Hakonarson H 2007-07-15 Nature www.ncbi.nlm.nih.gov/pubmed/17632545 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. Type 1 diabetes 467 European ancestry trios, 561 European ancestry cases, 1,143 European ancestry controls 390 European ancestry trios, 1,333 European ancestry cases from 549 families Illumina [543071] 4 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000054 Genome-wide genotyping array 2008-06-16 17637780 Winkelmann J 2007-07-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17637780 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Restless legs syndrome 401 European ancestry cases, 1,644 European ancestry controls 906 European ancestry cases, 891 European ancestry controls, 255 French Canadian cases, 287 French Canadian controls Affymetrix [236758] 3 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST000056 Genome-wide genotyping array 2010-03-30 20212171 Buil A 2010-03-08 Blood www.ncbi.nlm.nih.gov/pubmed/20212171 C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies. C4b binding protein levels 352 European ancestry related individuals NA Illumina [283437] 1 C4BP measurement http://www.ebi.ac.uk/efo/EFO_0004572 GCST000621 Genome-wide genotyping array 2010-04-14 20348956 Kiemeney LA 2010-03-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20348956 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. Urinary bladder cancer 1,889 European ancestry cases, 39,310 European ancestry controls 2,850 European ancestry cases, 6,239 European ancestry controls Illumina [304703] 3 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST000639 Genome-wide genotyping array 2015-05-20 21221126 Shen Y 2011-01-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/21221126 Genome-wide association study of serious blistering skin rash caused by drugs. Drug-induced Stevens-Johnson syndrome or toxic epidermal necrolysis (SJS/TEN) up to 72 European ancestry cases, up to 4,251 European ancestry controls NA Illumina [up to 1000000] 4 Stevens-Johnson syndrome, toxic epidermal necrolysis http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775 GCST000942 Genome-wide genotyping array 2012-02-14 22232737 Shu XO 2012-01-09 Cancer Res www.ncbi.nlm.nih.gov/pubmed/22232737 Novel genetic markers of breast cancer survival identified by a genome-wide association study. Breast cancer (survival) 1,950 Chinese ancestry cases 4,160 Chinese ancestry cases Affymetrix [613031] 3 event free survival time, survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000482, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST001373 Genome-wide genotyping array 2011-01-15 21203500 Lauc G 2010-12-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21203500 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. N-glycan levels 2,559 European ancestry individuals NA Illumina [~ 300000] 8 N-glycan measurement http://www.ebi.ac.uk/efo/EFO_0004999 GCST000925 Genome-wide genotyping array 2010-10-14 20871662 Fu YP 2010-09-02 J Ophthalmol www.ncbi.nlm.nih.gov/pubmed/20871662 Identification of Diabetic Retinopathy Genes through a Genome-Wide Association Study among Mexican-Americans from Starr County, Texas. Diabetic retinopathy 103 Mexican American cases, 183 Mexican American controls NA Affymetrix [421010] (imputed) 0 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST000786 Genome-wide genotyping array 2010-04-13 20360844 Arking DE 2010-03-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/20360844 Genome-wide association study identifies GPC5 as a novel genetic locus protective against sudden cardiac arrest. Sudden cardiac arrest 424 European ancestry cases, 226 European ancestry controls 521 cases and 19,090 controls of Black and European ancestry Affymetrix [1966233] (imputed) 0 sudden cardiac arrest http://www.ebi.ac.uk/efo/EFO_0004278 GCST000638 Genome-wide genotyping array 2009-04-23 19369658 Ikram MA 2009-04-15 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/19369658 Genomewide association studies of stroke. Stroke 1,164 European ancestry ischemic cases, 380 European ancestry cases, 18,058 European ancestry controls 259 African American ancestry ischemic cases, 41 African American ancestry cases, 2,704 African American ancestry controls, 652 European ancestry ischemic cases, 3,613 European ancestry controls Affymetrix, Illumina [2194468] (imputed) 4 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST000379 Genome-wide genotyping array 2010-04-27 20372150 Freathy RM 2010-04-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20372150 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. Birth weight 10,623 European ancestry individuals 27,591 European ancestry individuals, 1,415 Filipino ancestry individuals, 746 North African ancestry individuals, 333 Turkish ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 2 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST000648 Genome-wide genotyping array 2011-07-13 21572416 Kato N 2011-05-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21572416 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Blood pressure 19,608 East Asian ancestry individuals 30,765 East Asian ancestry individuals Affymetrix, Illumina [1700000] (imputed) 9 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST001072 Genome-wide genotyping array 2011-07-13 21572416 Kato N 2011-05-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21572416 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Blood pressure 19,608 East Asian ancestry individuals 30,765 East Asian ancestry individuals Affymetrix, Illumina [1700000] (imputed) 8 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST001074 Genome-wide genotyping array 2010-05-05 20383146 Kottgen A 2010-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20383146 New loci associated with kidney function and chronic kidney disease. Chronic kidney disease Up to 67,093 European ancestry individuals Up to 22,982 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 28 creatinine measurement, cystatin C measurement, chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0004617, http://www.ebi.ac.uk/efo/EFO_0003884 GCST000649 Genome-wide genotyping array 2009-03-31 19300482 Pillai SG 2009-03-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19300482 A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. Chronic obstructive pulmonary disease 823 cases, 810 controls 1,891 European ancestry individuals from 606 families, 389 European ancestry cases, 472 European ancestry controls, 949 individuals from 127 families Illumina [493609] 2 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST000359 Genome-wide genotyping array 2010-09-10 20673876 Rietschel M 2010-07-29 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20673876 Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression. Major depressive disorder 597 European ancestry cases, 1,295 European ancestry controls 409 European ancestry cases, 541 European ancestry controls Illumina [491238] 3 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST000743 Genome-wide genotyping array 2009-02-26 19165232 Otowa T 2009-01-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19165232 Genome-wide association study of panic disorder in the Japanese population. Panic disorder 200 Japanese ancestry cases, 200 Japanese ancestry controls NA Affymetrix [253903] 17 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST000320 Genome-wide genotyping array 2010-11-23 20923822 Niu N 2010-10-05 Genome Res www.ncbi.nlm.nih.gov/pubmed/20923822 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. Radiation response 93 African American human lymphoblastoid cell lines, 89 European ancestry human lymphoblastoid cell lines, 95 Han Chinese ancestry human lymphoblastoid cell lines NA Affymetrix, Illumina [1348798] 12 response to radiation http://purl.obolibrary.org/obo/GO_0009314 GCST000823 Genome-wide genotyping array 2009-09-09 19684573 Ge D 2009-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/19684573 Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. Response to hepatitis C treatment 871 European ancestry cases, 191 African American cases, 75 Hispanic cases NA Illumina [565759] 3 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST000465 Genome-wide genotyping array 2011-05-26 21544081 Dorajoo R 2011-04-19 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/21544081 Replication of 13 obesity loci among Singaporean Chinese, Malay and Asian-Indian populations. Obesity 5,429 Chinese ancestry individuals, 2,431 Malay ancestry individuals, 2,531 Asian Indian ancestry individuals NA Illumina [1283957] (imputed) 1 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001046 Genome-wide genotyping array 2009-03-30 19278955 Tregouet DA 2009-03-10 Blood www.ncbi.nlm.nih.gov/pubmed/19278955 Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. Venous thromboembolism 419 European ancestry cases, 1,228 European ancestry controls 1,757 European ancestry cases, 1,480 European ancestry controls Illumina [291872] 1 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST000354 Genome-wide genotyping array 2010-05-03 20363506 Meguro A 2010-04-02 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/20363506 Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. Glaucoma 305 Japanese ancestry cases, 355 Japanese ancestry controls NA Affymetrix [325947] 2 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST000645 Genome-wide genotyping array 2009-01-12 19060911 Aulchenko YS 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060911 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Cholesterol, total 21,848 European ancestry individuals, 714 Orcadian individuals NA Affymetrix, Illumina [up to 600000] 15 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST000285 Genome-wide genotyping array 2009-01-12 19060911 Aulchenko YS 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060911 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. LDL cholesterol 17,083 European ancestry individuals, 714 Orcadian individuals NA Affymetrix, Illumina [up to 600000] 12 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000282 Genome-wide genotyping array 2009-01-12 19060911 Aulchenko YS 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060911 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. Triglycerides 17,100 European ancestry individuals, 715 Orcadian individuals NA Affymetrix, Illumina [up to 600000] 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST000289 Genome-wide genotyping array 2009-01-12 19060911 Aulchenko YS 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060911 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. HDL cholesterol 20,697 European ancestry individuals, 715 Orcadian individuals NA Affymetrix, Illumina [up to 600000] 10 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000288 Genome-wide genotyping array 2011-01-16 21302353 Perroud N 2010-12-28 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21302353 Genome-wide association study of hoarding traits. Hoarding 3,304 European ancestry individuals NA Illumina [1517033] (imputed) 3 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST000932 Genome-wide genotyping array 2011-05-26 21471979 Kumar V 2011-04-07 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21471979 Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility. Large B-cell lymphoma 74 Japanese ancestry cases, 934 Japanese ancestry controls 325 Japanese ancestry cases, 3,309 Japanese ancestry controls Illumina [444361] 2 diffuse large B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000403 GCST001031 Genome-wide genotyping array 2009-01-21 19124843 Ober C 2009-01-07 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/19124843 Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q. Lp (a) levels 357 Hutterite individuals 1,054 European ancestry males Affymetrix [290327] 1 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST000312 Genome-wide genotyping array 2013-11-15 23704328 Fatemifar G 2013-05-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23704328 Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances. Primary tooth development (number of teeth) 11,513 European ancestry individuals Illumina [2446724] (imputed) 11 odontogenesis http://purl.obolibrary.org/obo/GO_0042476 GCST002031 Genome-wide genotyping array 2013-11-15 23704328 Fatemifar G 2013-05-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23704328 Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances. Primary tooth development (time to first tooth eruption) 11,118 European ancestry individuals Illumina [2446724] (imputed) 13 tooth eruption http://purl.obolibrary.org/obo/GO_0044691 GCST002030 Genome-wide genotyping array 2008-06-16 18264098 Gudmundsson J 2008-02-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18264098 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. Prostate cancer 1,854 European ancestry cases, 21,372 European ancestry controls 8,239 European ancestry cases, 7,590 European ancestry controls Illumina [310520] 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000153 Genome-wide genotyping array 2009-07-13 19571811 Purcell SM 2009-07-01 Nature www.ncbi.nlm.nih.gov/pubmed/19571811 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. Schizophrenia 3,322 European ancestry cases, 3,587 European ancestry controls 4,692 European ancestry cases, 15,493 European ancestry controls Affymetrix [739995] 4 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000434 Genome-wide genotyping array 2009-03-31 19287509 Cui J 2009-03-14 Mol Med www.ncbi.nlm.nih.gov/pubmed/19287509 Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis. Anti-cyclic Citrullinated Peptide Antibody 531 European ancestry cases 849 European ancestry cases Affymetrix [97248] 1 anti-cyclic citrullinated peptide antibody measurement http://www.ebi.ac.uk/efo/EFO_0004733 GCST000356 Genome-wide genotyping array 2009-09-30 19740415 Sha Q 2009-09-09 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/19740415 Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis. Amyotrophic lateral sclerosis (SNP x SNP interaction) 276 European ancestry cases, 271 European ancestry controls NA Illumina [549062] 0 sporadic amyotrophic lateral sclerosis http://www.ebi.ac.uk/efo/EFO_0001357 GCST000482 Genome-wide genotyping array 2008-06-16 18372903 Zeggini E 2008-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18372903 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. Type 2 diabetes 4,549 European ancestry cases, 5,579 European ancestry controls 24,194 European ancestry cases, 55,598 European ancestry controls Affymetrix, Illumina [2202892] (imputed) 16 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000167 Genome-wide genotyping array 2008-09-17 17903305 Murabito JM 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903305 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. Prostate cancer 59 cases, 558 controls NA Affymetrix [70897] 5 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000095 Genome-wide genotyping array 2008-09-10 17903305 Murabito JM 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903305 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. Breast cancer 58 cases, 665 controls NA Affymetrix [70897] 9 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000079 Genome-wide genotyping array 2008-12-01 18952825 Johansson A 2008-10-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/18952825 Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. Height 3,925 European ancestry individuals Up to 39,859 European ancestry individuals, Up to 1,148 African American individuals Illumina [NR] 1 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000254 Genome-wide genotyping array 2009-06-19 19508968 Zhai G 2009-06-08 J Med Genet www.ncbi.nlm.nih.gov/pubmed/19508968 A genome-wide association study suggests that a locus within the ataxin 2 binding protein 1 gene is associated with hand osteoarthritis: the Treat-OA consortium. Osteoarthritis 1,804 European ancestry individuals 3,266 European ancestry individuals Illumina [up to 535188] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST000421 Genome-wide genotyping array 2009-02-28 19185284 Ferrucci L 2009-01-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19185284 Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study. Carotenoid and tocopherol levels 1,191 European ancestry individuals 2,540 European ancestry individuals, 211 individuals Illumina [~ 500451] 2 carotenoid measurement, tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0004737, http://www.ebi.ac.uk/efo/EFO_0004738 GCST000324 Genome-wide genotyping array 2013-11-06 23658558 Bae HT 2013-05-08 Front Genet www.ncbi.nlm.nih.gov/pubmed/23658558 Genome-wide association study of personality traits in the long life family study. Personality dimensions Up to 2,631 European ancestry individuals up to 1,287 European ancestry individuals, 1,084 individuals Illumina [up to 38045518] (imputed) 0 personality trait http://www.ebi.ac.uk/efo/EFO_0004365 GCST002015 Genome-wide genotyping array 2013-11-06 23658558 Bae HT 2013-05-08 Front Genet www.ncbi.nlm.nih.gov/pubmed/23658558 Genome-wide association study of personality traits in the long life family study. Personality dimensions Up to 4,595 European ancestry individuals 1,045 individuals Illumina [up to 40038518] (imputed) 0 personality trait http://www.ebi.ac.uk/efo/EFO_0004365 GCST002016 Genome-wide genotyping array 2009-05-19 19430483 Newton-Cheh C 2009-05-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19430483 Genome-wide association study identifies eight loci associated with blood pressure. Systolic blood pressure 34,433 European ancestry individuals Up to 100,347 European ancestry individuals, up to 12,889 Indian Asian ancestry individuals Affymetrix, Illumina [2497993] (imputed) 3 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST000395 Genome-wide genotyping array 2009-05-19 19430483 Newton-Cheh C 2009-05-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19430483 Genome-wide association study identifies eight loci associated with blood pressure. Diastolic blood pressure 34,433 European ancestry individuals Up to 100,347 European ancestry individuals, up to 12,889 Indian Asian ancestry individuals Affymetrix, Illumina [2497993] (imputed) 6 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST000394 Genome-wide genotyping array 2009-04-10 18711366 Unoki H 2008-08-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18711366 SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. Type 2 diabetes 194 Japanese ancestry cases, 1,558 Japanese ancestry controls 5,324 East Asian ancestry cases, 7,037 East Asian ancestry controls, 4,085 European ancestry cases, 5,302 European ancestry controls Affymetrix [207097] 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000221 Genome-wide genotyping array 2012-09-25 22843789 Baldwin RM 2012-07-27 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/22843789 A genome-wide association study identifies novel loci for paclitaxel-induced sensory peripheral neuropathy in CALGB 40101. Paclitaxel-induced neuropathy 855 European ancestry breast cancer cases 154 European ancestry breast cancer cases, 117 African American breast cancer cases Illumina [521600] 0 methylcobalamin deficiency type cblE, neuropathy http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0004149 GCST001624 Genome-wide genotyping array 2008-12-09 18997785 Aulchenko YS 2008-11-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18997785 Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. Multiple sclerosis 45 European ancestry cases,195 European ancestry controls 1,316 European ancestry cases, 1,423 European ancestry controls, 1,318 cases and 1,507 controls from 756 families Affymetrix [~ 250000] 1 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000263 Genome-wide genotyping array 2009-03-30 19300499 Takeuchi F 2009-03-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19300499 A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose. Warfarin maintenance dose 1,053 European ancestry individuals 588 European ancestry individuals Illumina [325997] 4 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST000360 Genome-wide genotyping array 2008-06-16 17603485 Gudmundsson J 2007-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17603485 Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes. Prostate cancer 1,501 European ancestry cases, 11,290 European ancestry controls 1,992 European ancestry cases, 3,058 European ancestry controls Illumina [310520] 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000050 Genome-wide genotyping array 2009-05-14 19416921 Scott LJ 2009-05-05 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/19416921 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. Bipolar disorder 3,683 European ancestry cases, 14,507 European ancestry controls NA Affymetrix, Illumina [2366197] (imputed) 13 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000387 Genome-wide genotyping array 2009-09-14 19654303 Broderick P 2009-08-04 Cancer Res www.ncbi.nlm.nih.gov/pubmed/19654303 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. Lung cancer 1,952 European ancestry cases, 1,438 European ancestry controls 2,465 European ancestry cases, 3,005 European ancestry controls, 3,143 individuals, 3,762 individuals Illumina [511919] 7 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000459 Genome-wide genotyping array 2009-09-28 18403759 Ober C 2008-04-09 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/18403759 Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function. YKL-40 levels 632 Hutterite individuals 443 European ancestry cases, 491 European ancestry controls, 206 European ancestry individuals Affymetrix [290325] 1 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST000177 Genome-wide genotyping array 2009-01-16 19010793 Baranzini SE 2008-11-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19010793 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Multiple sclerosis 978 European ancestry cases, 883 European ancestry controls NA Illumina [551642] 10 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000269 Genome-wide genotyping array 2009-01-16 19010793 Baranzini SE 2008-11-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19010793 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Multiple sclerosis (age of onset) 978 European ancestry cases, 883 European ancestry controls NA Illumina [551642] 8 age of onset of multiple sclerosis http://purl.obolibrary.org/obo/OBA_2001029 GCST000267 Genome-wide genotyping array 2009-01-16 19010793 Baranzini SE 2008-11-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19010793 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Normalized brain volume 753 European ancestry cases, 883 European ancestry controls NA Illumina [551642] 5 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000268 Genome-wide genotyping array 2009-01-16 19010793 Baranzini SE 2008-11-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19010793 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Brain lesion load 791 European ancestry cases, 883 European ancestry controls NA Illumina [551642] 4 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000265 Genome-wide genotyping array 2009-01-16 19010793 Baranzini SE 2008-11-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19010793 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Multiple sclerosis (severity) 794 European ancestry cases, 883 European ancestry controls NA Illumina [551642] 11 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000266 Genome-wide genotyping array 2010-09-07 20639881 Conde L 2010-07-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20639881 Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. Follicular lymphoma 681 European ancestry cases, 750 European ancestry controls up to 3,164 European ancestry cases, 6,208 European ancestry controls Illumina [312768] 3 neoplasm of mature B-cells http://www.ebi.ac.uk/efo/EFO_0000096 GCST000734 Genome-wide genotyping array 2008-09-08 18439552 Reiner AP 2008-04-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18439552 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. C-reactive protein 909 European ancestry individuals 5,106 European ancestry individuals Illumina [317000] 3 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST000179 Genome-wide genotyping array 2010-02-28 20081858 Dupuis J 2010-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20081858 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Fasting blood insulin 38,238 European ancestry individuals 62,264 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST000571 Genome-wide genotyping array 2010-02-28 20081858 Dupuis J 2010-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20081858 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Fasting blood glucose 46,186 European ancestry individuals 76,558 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 16 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000568 Genome-wide genotyping array 2018-01-23 20081858 Dupuis J 2010-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20081858 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Homeostasis model assessment of insulin resistance 37,037 European ancestry individuals 62,264 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 HOMA-IR http://www.ebi.ac.uk/efo/EFO_0004501 GCST005179 Genome-wide genotyping array 2018-01-23 20081858 Dupuis J 2010-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20081858 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Homeostasis model assessment of beta-cell function 36,466 European ancestry individuals 62,264 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 10 HOMA-B http://www.ebi.ac.uk/efo/EFO_0004469 GCST005180 Genome-wide genotyping array 2008-08-11 18677311 O'Donovan MC 2008-07-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18677311 Identification of loci associated with schizophrenia by genome-wide association and follow-up. Schizophrenia 479 European ancestry cases, 2,937 European ancestry controls 4,143 European ancestry cases, 6,515 European ancestry controls, 1,782 East Asian ancestry cases, 1,865 East Asian ancestry controls, 741 cases, 1,517 controls Affymetrix [362532] 3 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000215 Genome-wide genotyping array 2009-12-04 19897590 Schaefer AS 2009-11-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19897590 A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis. Periodontitis 283 European ancestry cases, 972 European ancestry controls 155 European ancestry cases, 341 European ancestry controls Affymetrix [345646] 1 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST000521 Genome-wide genotyping array 2008-06-10 18455228 Richards JB 2008-04-29 Lancet www.ncbi.nlm.nih.gov/pubmed/18455228 Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study. Bone mineral density 2,094 European ancestry female individuals 6,463 European ancestry individuals Illumina [314075] 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000182 Genome-wide genotyping array 2010-02-04 20068591 Van Laer L 2010-01-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20068591 A genome-wide association study for age-related hearing impairment in the Saami. Hearing impairment 347 Finnish Saami individuals NA Affymetrix [83381] 2 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST000566 Genome-wide genotyping array 2012-02-21 22282500 Chien JW 2012-01-26 Blood www.ncbi.nlm.nih.gov/pubmed/22282500 Evaluation of published single nucleotide polymorphisms associated with acute GVHD. Acute graft versus host disease 1,298 Allogenic hematopoietic cell transplantation donors and recipients NA Affymetrix [NR] (imputed) 0 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST001386 Genome-wide genotyping array 2008-06-16 18311140 Hunt KA 2008-03-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18311140 Newly identified genetic risk variants for celiac disease related to the immune response. Celiac disease 767 European ancestry cases, 1,422 European ancestry controls 1,643 European ancestry cases, 3,406 European ancestry controls Illumina [310605] 8 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST000157 Genome-wide genotyping array 2008-06-27 18488028 Sulem P 2008-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18488028 Two newly identified genetic determinants of pigmentation in Europeans. Blue vs. green eyes 5,130 Icelandic individuals 3,330 European ancestry individuals Illumina [316515] 1 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST000192 Genome-wide genotyping array 2008-06-27 18488028 Sulem P 2008-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18488028 Two newly identified genetic determinants of pigmentation in Europeans. Burning and freckling 5,130 Icelandic individuals 3,330 European ancestry individuals Illumina [316515] 1 freckles, sunburn http://www.ebi.ac.uk/efo/EFO_0003963, http://www.ebi.ac.uk/efo/EFO_0003958 GCST000196 Genome-wide genotyping array 2008-07-01 18488028 Sulem P 2008-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18488028 Two newly identified genetic determinants of pigmentation in Europeans. Freckles 5,130 Icelandic individuals 3,330 European ancestry individuals Illumina [316515] 1 freckles http://www.ebi.ac.uk/efo/EFO_0003963 GCST000197 Genome-wide genotyping array 2008-07-01 18488028 Sulem P 2008-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18488028 Two newly identified genetic determinants of pigmentation in Europeans. Skin sensitivity to sun 5,130 Icelandic individuals 3,330 European ancestry individuals Illumina [316515] 1 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST000195 Genome-wide genotyping array 2008-06-27 18488028 Sulem P 2008-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18488028 Two newly identified genetic determinants of pigmentation in Europeans. Blond vs. brown hair color 5,130 European ancestry individuals 3,330 European ancestry individuals Illumina [316515] 1 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST000194 Genome-wide genotyping array 2008-06-27 18488028 Sulem P 2008-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18488028 Two newly identified genetic determinants of pigmentation in Europeans. Red vs. non-red hair color 5,130 European ancestry individuals 3,330 European ancestry individuals Illumina [316515] 1 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST000193 Genome-wide genotyping array 2012-03-10 22228203 Aslibekyan S 2012-01-05 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/22228203 A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network. Inflammatory biomarkers 1,092 European ancestry individuals NA Affymetrix [2543887] (imputed) 19 response to fenofibrate http://purl.obolibrary.org/obo/GO_1901557 GCST001371 Genome-wide genotyping array 2008-06-18 18488026 Brown KM 2008-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18488026 Common sequence variants on 20q11.22 confer melanoma susceptibility. Melanoma 864 European ancestry cases, 864 European ancestry controls 1,230 European ancestry cases, 1,251 European ancestry controls Illumina [535150] 1 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST000198 Genome-wide genotyping array 2011-01-12 21131588 Slager SL 2010-12-03 Blood www.ncbi.nlm.nih.gov/pubmed/21131588 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. Chronic lymphocytic leukemia 407 European ancestry cases, 296 European ancestry controls 252 European ancestry cases, 965 European ancestry controls Affymetrix [827777] 4 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST000906 Genome-wide genotyping array 2013-11-29 23727862 Savage SA 2013-06-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23727862 Genome-wide association study identifies two susceptibility loci for osteosarcoma. Osteosarcoma 694 European ancestry cases, 2,703 European ancestry controls 247 European ancestry cases, 550 European ancestry controls Illumina [698968] 6 osteosarcoma http://www.ebi.ac.uk/efo/EFO_0000637 GCST002056 Genome-wide genotyping array 2011-01-18 21151130 Painter JN 2010-12-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21151130 Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. Endometriosis 3,194 European ancestry cases, 7,060 European ancestry controls 2,392 European ancestry cases, 2,271 European ancestry controls Illumina [504723] 3 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST000916 Genome-wide genotyping array 2015-05-23 21208937 Pichler I 2011-01-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21208937 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. Iron status biomarkers Up to 5,633 European ancestry individuals Up to 3,457 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 5 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST000935 Genome-wide genotyping array 2009-10-06 19779542 Nakanishi H 2009-09-25 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19779542 A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1. Myopia (pathological) 297 Japanese ancestry cases, 934 Japanese ancestry controls 533 Japanese ancestry cases, 977 Japanese ancestry controls Illumina [411777] 1 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST000491 Genome-wide genotyping array 2009-09-28 19729612 Paterson AD 2009-09-03 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/19729612 Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. Soluble E-selectin levels 685 European ancestry individuals with type 1 diabetes 477 European ancestry individuals Illumina [~ 841000] 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST000476 Genome-wide genotyping array 2011-12-24 22144915 Fan Q 2011-12-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22144915 Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. Corneal astigmatism 1,231 Chinese ancestry cases, 785 Chinese ancestry controls, 1,018 Malay ancestry cases, 1,220 Malay ancestry controls 825 Indian ancestry cases, 1,314 Indian ancestry controls, 760 Chinese ancestry child cases, 169 Chinese ancestry child controls, 397 Chinese ancestry trios Illumina [460528] 6 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST001339 Genome-wide genotyping array 2010-07-01 20529992 Teupser D 2010-06-07 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20529992 Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Phytosterol levels 1,495 European ancestry individuals 2,917 European ancestry individuals Affymetrix [374370] 3 phytosterol measurement http://www.ebi.ac.uk/efo/EFO_0004862 GCST000694 Genome-wide genotyping array 2011-06-23 21674006 Yamada K 2011-06-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/21674006 Genome-wide association study of schizophrenia in Japanese population. Schizophrenia 120 Japanese ancestry trios 1,083 East Asian ancestry cases, 1,092 East Asian ancestry controls Affymetrix [97963] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001090 Genome-wide genotyping array 2013-07-12 23565138 Trzaskowski M 2013-04-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/23565138 First genome-wide association study on anxiety-related behaviours in childhood. Anxiety 2,810 European ancestry children 4,804 European ancestry children Affymetrix [~ 2500000] (imputed) 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST001948 Genome-wide genotyping array 2011-04-11 21378988 Coronary Artery Disease (C4D) Genetics Consortium 2011-03-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21378988 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. Coronary heart disease 8,424 European ancestry cases, 7,268 European ancestry controls, 6,996 South Asian ancestry cases, 7,794 South Asian ancestry controls 18,049 European ancestry cases, 16,357 European ancestry controls, 3,359 South Asian ancestry cases, 2,828 South Asian ancestry controls Illumina [574919] 19 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST000999 Genome-wide genotyping array 2010-05-06 20385826 Neale BM 2010-04-12 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/20385826 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). Age-related macular degeneration 979 cases, 1,709 controls 868 European ancestry cases, 410 European ancestry controls, 4,921 cases, 3,824 controls Affymetrix [632932] 11 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST000653 Genome-wide genotyping array 2010-09-21 20694011 Ferreira RC 2010-08-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20694011 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. Immunoglobulin A 430 European ancestry cases, 1,090 European ancestry controls 342 European ancestry cases, 886 European ancestry controls Illumina [2057134] (imputed) 12 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST000763 Genome-wide genotyping array 2009-08-21 19625618 Nakano M 2009-07-22 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/19625618 Three susceptible loci associated with primary open-angle glaucoma identified by genome-wide association study in a Japanese population. Glaucoma (primary open-angle) 418 Japanese ancestry cases, 300 Japanese ancestry controls 409 Japanese ancestry cases, 448 Japanese ancestry controls Affymetrix [331838] 0 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST000449 Genome-wide genotyping array 2010-09-01 20637204 Ochi H 2010-07-13 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/20637204 ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients. Ribavirin-induced anemia 453 Japanese ancestry individuals 470 Japanese ancestry individuals Illumina [510537] 1 anemia (phenotype), response to ribavirin http://www.ebi.ac.uk/efo/EFO_0004272, http://purl.obolibrary.org/obo/GO_1901559 GCST000729 Genome-wide genotyping array 2011-01-04 21061259 Plant D 2010-11-08 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/21061259 Genome-wide association study of genetic predictors of anti-tumor necrosis factor treatment efficacy in rheumatoid arthritis identifies associations with polymorphisms at seven loci. Response to anti-TNF therapy in rheumatoid arthritis 566 European ancestry individuals 720 European ancestry individuals Affymetrix [459446] 0 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST000865 Genome-wide genotyping array 2011-12-20 22095909 Lange CM 2011-11-16 Hepatology www.ncbi.nlm.nih.gov/pubmed/22095909 Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy. Response to hepatitis C treatment 707 European ancestry cases NA NR [NR] 9 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST001325 Genome-wide genotyping array 2010-02-28 20112360 Kerkhof HJ 2010-01-07 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/20112360 A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22. Osteoarthritis 1,341 European ancestry cases, 3,496 European ancestry controls 9,779 European ancestry cases, up to 31,818 European ancestry controls, 3,818 cases, 7,278 controls Illumina [500510] 1 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST000558 Genome-wide genotyping array 2009-05-20 19426955 Himes BE 2009-05-07 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19426955 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. Asthma 359 European ancestry cases, 846 European ancestry controls 2,981 European ancestry cases, 12,358 European ancestry controls, 769 European ancestry and hispanic cases, 1,007 European ancestry and hispanic controls, 592 Hispanic cases with their 1,184 Hispanic parental controls, 2,258 African American cases, 3,006 African American controls Illumina [518230] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000389 Genome-wide genotyping array 2009-07-24 19587794 Nolte IM 2009-07-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/19587794 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. QT interval 3,558 European ancestry individuals 29,527 European ancestry individuals Affymetrix, Illumina [~ 2399142] (imputed) 2 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST000444 Genome-wide genotyping array 2013-06-18 23703922 Li WD 2013-01-02 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/23703922 A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls. Uric acid levels 487 European ancestry obese individuals, 472 non-obese individuals NA Illumina [~ 550000] 6 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST001801 Genome-wide genotyping array 2013-01-31 23118302 Chu AY 2012-11-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23118302 Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy. Lipoprotein-associated phospholipase A2 activity change in response to statin therapy 2,673 European ancestry cases, 2,656 European ancestry controls NA Illumina [796174] 7 lipoprotein-associated phospholipase A(2) measurement http://www.ebi.ac.uk/efo/EFO_0004746 GCST001726 Genome-wide genotyping array 2013-01-30 23118302 Chu AY 2012-11-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23118302 Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy. Lipoprotein-associated phospholipase A2 activity and mass 6,851 European ancestry individuals 13,664 European ancestry individuals Illumina [796174] 9 lipoprotein-associated phospholipase A(2) measurement http://www.ebi.ac.uk/efo/EFO_0004746 GCST001727 Genome-wide genotyping array 2013-05-14 21618603 Beaty TH 2011-05-26 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/21618603 Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. Orofacial clefts (maternal alcohol consumption interaction) 272 European ancestry trios, 259 Asian ancestry trios, 19 African ancestry or other ancestry trios NA Illumina [~ 498000] 2 obsolete Mendelian syndromes with cleft lip/palate, alcohol consumption measurement, cleft lip http://purl.obolibrary.org/obo/MONDO_0015335, http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0003959 GCST001082 Genome-wide genotyping array 2008-06-16 18385676 Amos CI 2008-04-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18385676 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. Lung cancer 1,154 European ancestry cases, 1,137 European ancestry controls 2,724 European ancestry cases, 3,694 European ancestry controls Illumina [317498] 3 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000172 Genome-wide genotyping array 2011-04-29 21460395 Gu J 2011-04-02 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/21460395 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. Telomere length 459 individuals 1,160 individuals Illumina [312531] 4 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST001024 Genome-wide genotyping array 2011-03-28 21348951 Parsa A 2011-02-01 Clin Transl Sci www.ncbi.nlm.nih.gov/pubmed/21348951 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. Cardiac hypertrophy 851 Old Order Amish individuals NA Affymetrix [361034] 19 cardiac hypertrophy http://www.ebi.ac.uk/efo/EFO_0002503 GCST000960 Genome-wide genotyping array 2011-01-11 21057379 Curtis D 2010-11-04 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21057379 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. Bipolar disorder and schizophrenia 506 European ancestry bipolar 1 disorder cases, 523 European ancestry schizophrenia cases, 505 European ancestry controls NA Affymetrix [302482] 6 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST000862 Genome-wide genotyping array 2009-03-31 19305408 Newton-Cheh C 2009-03-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19305408 Common variants at ten loci influence QT interval duration in the QTGEN Study. QT interval 13,685 European ancestry individuals 15,854 European ancestry individuals Affymetrix, Illumina [up to 2543686] (imputed) 13 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST000363 Genome-wide genotyping array 2009-11-25 19846067 Garriock HA 2009-10-19 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19846067 A genomewide association study of citalopram response in major depressive disorder. Response to citalopram treatment Up to 659 European ancestry responders, up to 121 African American responders, up to 103 Hispanic responders, 408 European ancestry non-responders, 120 African American non-responders, 80 Hispanic non-responders NA Affymetrix [430198] 7 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST000509 Genome-wide genotyping array 2009-06-01 19448623 Ong KK 2009-05-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19448623 Genetic variation in LIN28B is associated with the timing of puberty. Menarche (age at onset) 4,714 European ancestry female individuals 16,373 European ancestry female individuals Affymetrix [up to 390631] 1 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST000405 Genome-wide genotyping array 2009-11-09 19836008 Landi MT 2009-10-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19836008 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. Lung adenocarcinoma 5,739 European ancestry cases, 5,848 European ancestry controls 7,561 European ancestry cases, 13,818 European ancestry controls Illumina [515922] 5 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST000506 Genome-wide genotyping array 2008-06-16 17435756 Rioux JD 2007-04-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17435756 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. Crohn's disease 946 cases, 977 controls 530 trios, 353 cases, 207 controls Illumina [304413] 4 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000023 Genome-wide genotyping array 2008-11-12 18835860 Mushiroda T 2008-10-01 J Med Genet www.ncbi.nlm.nih.gov/pubmed/18835860 A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. Idiopathic pulmonary fibrosis 159 Japanese ancestry cases, 934 Japanese ancestry controls 83 Japanese ancestry cases, 535 Japanese ancestry controls Illumina [214508] 1 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST000238 Genome-wide genotyping array 2008-12-30 19009022 Drgon T 2008-11-09 Mol Med www.ncbi.nlm.nih.gov/pubmed/19009022 Genome-wide association for nicotine dependence and smoking cessation success in NIH research volunteers. Nicotine dependence 220 European ancestry cases, 260 European ancestry controls NA Affymetrix [~ 60000] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST000264 Genome-wide genotyping array 2009-01-14 19114657 Wang Y 2008-12-29 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/19114657 From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. Blood pressure 542 Old Order Amish individuals 5,229 European ancestry individuals, 1,347 Amish individuals, 575 Hutterite individuals Affymetrix [79447] 1 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST000306 Genome-wide genotyping array 2011-04-12 21399635 Mells GF 2011-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21399635 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. Primary biliary cholangitis 1,840 European ancestry cases, 5,163 European ancestry controls and (Liu et al) 620 European ancestry cases, 2,514 European ancestry controls Illumina [507467] 21 biliary liver cirrhosis http://www.ebi.ac.uk/efo/EFO_0004267 GCST001010 Genome-wide genotyping array 2008-08-11 18668548 Julia A 2008-08-01 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/18668548 Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility. Rheumatoid arthritis 400 European ancestry cases, 400 European ancestry controls 410 European ancestry cases, 394 European ancestry controls Illumina [299918] 2 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000217 Genome-wide genotyping array 2013-03-26 23321320 Urabe Y 2013-01-12 J Hepatol www.ncbi.nlm.nih.gov/pubmed/23321320 A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region. Hepatitis C induced liver cirrhosis 682 Japanese ancestry cases, 1,045 Japanese ancestry controls 936 Japanese ancestry cases, 3,809 Japanese ancestry controls Illumina [431618] 5 hepatitis C induced liver cirrhosis http://www.ebi.ac.uk/efo/EFO_0005129 GCST001815 Genome-wide genotyping array 2009-09-28 17407593 Uhl GR 2007-04-03 BMC Genet www.ncbi.nlm.nih.gov/pubmed/17407593 Molecular genetics of nicotine dependence and abstinence: whole genome association using 520,000 SNPs. Nicotine dependence 134 European ancestry cases, 320 European ancestry controls NA Affymetrix [~ 520000] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST000021 Genome-wide genotyping array 2008-09-08 17474819 Coon KD 2007-04-01 J Clin Psychiatry www.ncbi.nlm.nih.gov/pubmed/17474819 A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. Alzheimer's disease (late onset) 664 European ancestry cases, 422 European ancestry controls NA Affymetrix [~ 502627] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000018 Genome-wide genotyping array 2009-09-30 19754311 Le Clerc S 2009-09-15 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/19754311 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). AIDS 85 European ancestry cases, 2,049 European ancestry controls NA Illumina [291119] 7 AIDS http://www.ebi.ac.uk/efo/EFO_0000765 GCST000487 Genome-wide genotyping array 2010-03-25 20189936 Okada Y 2010-02-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20189936 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. Height 19,633 Japanese ancestry individuals NA Illumina [420885] 25 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000611 Genome-wide genotyping array 2009-06-04 19448621 He C 2009-05-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19448621 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. Menarche and menopause (age at onset) 17,438 European ancestry female individuals NA Illumina [317759] 6 age at menarche, age at menopause http://www.ebi.ac.uk/efo/EFO_0004703, http://www.ebi.ac.uk/efo/EFO_0004704 GCST000403 Genome-wide genotyping array 2009-01-14 19060910 Sabatti C 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060910 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. HDL cholesterol 4,763 Northern Finnish founder individuals NA Illumina [329091] 5 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000284 Genome-wide genotyping array 2009-01-14 19060910 Sabatti C 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060910 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. LDL cholesterol 4,763 Northern Finnish founder individuals NA Illumina [329091] 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000283 Genome-wide genotyping array 2009-01-14 19060910 Sabatti C 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060910 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. Metabolic traits 4,763 Northern Finnish founder individuals NA Illumina [329091] 11 inflammatory response, triglyceride measurement, insulin measurement, glucose measurement http://purl.obolibrary.org/obo/GO_0006954, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004467, http://www.ebi.ac.uk/efo/EFO_0004468 GCST000292 Genome-wide genotyping array 2008-06-23 17395743 Hanson RL 2007-04-01 Diabetes www.ncbi.nlm.nih.gov/pubmed/17395743 Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study. End-stage renal disease 105 Pima Indian ancestry cases, 102 Pima Indian ancestry controls NA Affymetrix [115352] 1 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST000020 Genome-wide genotyping array 2009-05-28 19448619 Stolk L 2009-05-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19448619 Loci at chromosomes 13, 19 and 20 influence age at natural menopause. Menopause (age at onset) 2,979 European ancestry female individuals 2,560 European ancestry female individuals Illumina [315418] 13 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST000401 Genome-wide genotyping array 2008-06-16 17401363 Yeager M 2007-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17401363 Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. Prostate cancer 1,172 European ancestry cases, 1,157 European ancestry controls 3,124 European ancestry cases, 3,142 European ancestry controls Illumina [538548] 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000017 Genome-wide genotyping array 2008-09-15 17975299 Webster JA 2007-11-01 Neurodegener Dis www.ncbi.nlm.nih.gov/pubmed/17975299 Sorl1 as an Alzheimer's disease predisposition gene? Alzheimer's disease 664 cases, 422 controls NA Affymetrix [~ 502627] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000121 Genome-wide genotyping array 2008-09-09 17357082 Melquist S 2007-03-08 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/17357082 Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms. Progressive supranuclear palsy 288 European ancestry cases, 344 European ancestry controls 213 European ancestry cases, 391 European ancestry controls Affymetrix [428867] 0 progressive supranuclear palsy http://purl.obolibrary.org/obo/MONDO_0019037 GCST000015 Genome-wide genotyping array 2009-03-01 19198609 Kathiresan S 2009-02-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19198609 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Myocardial infarction (early onset) 2,967 European ancestry cases, 3,075 European ancestry controls 9,746 European ancestry cases, 9,746 European ancestry controls Affymetrix [~ 2500000] (imputed) 9 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST000340 Genome-wide genotyping array 2009-07-01 19553259 Cotsapas C 2009-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19553259 Common body mass index-associated variants confer risk of extreme obesity. Obesity (extreme) 775 European ancestry cases, 3,197 European ancestry controls NA Illumina [457251] 13 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST000426 Genome-wide genotyping array 2008-06-22 18454146 Chambers JC 2008-05-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18454146 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. Waist circumference and related phenotypes 2,684 Indian Asian ancestry male individuals 7,394 Indian Asian ancestry individuals, 4,561 European ancestry individuals Illumina [308067] 4 waist circumference, triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST000184 Genome-wide genotyping array 2009-09-30 20061627 Heinzen EL 2009-09-11 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/20061627 Genome-wide scan of copy number variation in late-onset Alzheimer's disease. Alzheimer's disease 331 European ancestry cases, 368 European ancestry controls NA Illumina [~ 550000] 5 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000484 Genome-wide genotyping array 2011-01-11 21150878 Ferreira MA 2010-12-08 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21150878 Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia. Asthma 986 European ancestry cases, 1,846 European ancestry controls 391 European ancestry cases, 213 European ancestry controls Illumina [~ 2380000] (imputed) 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000910 Genome-wide genotyping array 2009-06-15 19483685 Daly AK 2009-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19483685 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. Drug-induced liver injury (flucloxacillin) 58 European ancestry cases, 282 European ancestry controls NA Illumina [866399] 6 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST000415 Genome-wide genotyping array 2009-02-27 19196962 Garcia-Barcelo MM 2009-02-05 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/19196962 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. Hirschsprung disease 181 Chinese ancestry cases, 346 Chinese ancestry controls 190 Chinese ancestry cases, 510 Chinese ancestry controls Affymetrix [293836] 2 Hirschsprung disease http://purl.obolibrary.org/obo/MONDO_0018309 GCST000334 Genome-wide genotyping array 2009-12-29 20031577 Danik JS 2009-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031577 Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study. Fibrinogen 17,686 European ancestry female individuals NA Illumina [337343] 6 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST000368 Genome-wide genotyping array 2009-01-14 19110211 Meisinger C 2008-12-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/19110211 A genome-wide association study identifies three loci associated with mean platelet volume. Mean platelet volume 1,606 European ancestry individuals 8,617 European ancestry individuals Affymetrix [335152] 3 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST000305 Genome-wide genotyping array 2009-10-16 19801982 Rivadeneira F 2009-10-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19801982 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. Bone mineral density (hip) 19,195 European ancestry individuals NA Affymetrix, Illumina [2543686] (imputed) 13 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000495 Genome-wide genotyping array 2009-10-16 19801982 Rivadeneira F 2009-10-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19801982 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. Bone mineral density (spine) 19,195 European ancestry individuals NA Affymetrix, Illumina [2543686] (imputed) 16 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000494 Genome-wide genotyping array 2012-03-03 22306654 Feenstra B 2012-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22306654 Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis. Infantile hypertrophic pyloric stenosis 1,001 European ancestry cases, 2,401 European ancestry controls 796 European ancestry cases, 876 European ancestry controls Illumina [523420] 5 infantile hypertrophic pyloric stenosis http://www.ebi.ac.uk/efo/EFO_0004707 GCST001399 Genome-wide genotyping array 2009-09-09 19668339 Potkin SG 2009-08-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. Hippocampal atrophy 162 European ancestry cases, 192 European ancestry controls, 7 African American cases, 14 African American controls, 1 Asian ancestry cases, 3 Asian ancestry controls, 2 cases NA Illumina [516645] 21 hippocampal atrophy http://www.ebi.ac.uk/efo/EFO_0005039 GCST000461 Genome-wide genotyping array 2009-07-01 19561606 Thorleifsson G 2009-06-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19561606 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. Kidney stones 1,507 European ancestry cases, 34,033 European ancestry controls 2,266 European ancestry cases, 8,477 European ancestry controls Illumina [303120] 1 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST000429 Genome-wide genotyping array 2012-09-21 22760553 Adkins DE 2012-07-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/22760553 Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D. Response to citalopram treatment 1,392 European ancestry depression cases, 264 African American depression cases, 106 depression cases NA Affymetrix [421789] 17 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST001591 Genome-wide genotyping array 2010-01-19 20041166 Fellay J 2009-12-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20041166 Common genetic variation and the control of HIV-1 in humans. HIV-1 control 2,362 European ancestry cases NA Illumina [NR] 42 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST000549 Genome-wide genotyping array 2009-01-15 19079260 Thorleifsson G 2008-12-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19079260 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. Weight 72,598 European ancestry individuals, 1,160 African American individuals Up to 11,036 European ancestry individuals, 32,615 individuals Illumina [305846] 17 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST000299 Genome-wide genotyping array 2009-01-15 19079260 Thorleifsson G 2008-12-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19079260 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. Body mass index 72,598 European ancestry individuals, 1,160 African American individuals Up to 11,036 European ancestry individuals, 32,615 individuals Illumina [305846] 14 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000296 Genome-wide genotyping array 2009-06-29 19525953 De Jager PL 2009-06-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19525953 Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. Multiple sclerosis 2,624 European ancestry cases, 7,220 European ancestry controls 2,215 European ancestry cases, 2,116 European ancestry controls Affymetrix, Illumina [~ 2560000] (imputed) 15 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000424 Genome-wide genotyping array 2010-10-14 20860503 Moffatt MF 2010-09-23 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/20860503 A large-scale, consortium-based genomewide association study of asthma. Asthma 10,365 cases, 16,110 controls NA Illumina [582892] 10 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000804 Genome-wide genotyping array 2012-11-04 22951595 Hwang JY 2012-09-06 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22951595 Genome-wide association study identifies GYS2 as a novel genetic factor for polycystic ovary syndrome through obesity-related condition. Polycystic ovary syndrome 774 Korean ancestry cases, 967 Korean ancestry controls 482 Korean ancestry children, 468 Korean ancestry pregnant female individuals, 1,242 Korean ancestry female controls Illumina [~ 3091653] (imputed) 0 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST001669 Genome-wide genotyping array 2011-09-17 21826061 Davies G 2011-08-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21826061 Genome-wide association studies establish that human intelligence is highly heritable and polygenic. Intelligence 3,511 European ancestry individuals 670 European ancestry individuals Illumina [549692] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST001195 Genome-wide genotyping array 2011-06-14 21612516 Malovini A 2011-05-25 Rejuvenation Res www.ncbi.nlm.nih.gov/pubmed/21612516 Association study on long-living individuals from Southern Italy identifies rs10491334 in the CAMKIV gene that regulates survival proteins. Longevity 410 European ancestry long-living individuals, 553 European ancestry young individuals 116 European ancestry long-living individuals, 160 European ancestry young individuals Illumina [298715] 1 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST001081 Genome-wide genotyping array 2011-06-08 21611967 Gupta M 2011-05-24 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/21611967 Identification of homogeneous genetic architecture of multiple genetically correlated traits by block clustering of genome-wide associations. Fracture-related traits 2,038 indivduals NA Affymetrix [433510] 0 bone fracture related measurement http://www.ebi.ac.uk/efo/EFO_0004516 GCST001080 Genome-wide genotyping array 2011-06-07 21602797 Wright FA 2011-05-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21602797 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. Cystic fibrosis severity 2,317 European ancestry cases, 177 cases 898 European ancestry sibling pair cases, 75 sibling pair cases Illumina [~ 2609000] (imputed) 6 cystic fibrosis http://purl.obolibrary.org/obo/MONDO_0009061 GCST001077 Genome-wide genotyping array 2013-05-26 23509613 Kamboh MI 2013-02-24 Autoimmune Dis www.ncbi.nlm.nih.gov/pubmed/23509613 Genome-wide association study of antiphospholipid antibodies. Presence of antiphospholipid antibodies 183 European ancestry ACL-positive cases, 487 European ancestry ACL-negative controls, 127 European ancestry LAC-positive cases, 581 European ancestry LAC-negative controls, 136 European ancestry Anti-B2GPI-positive cases, 360 European ancestry Anti-B2GPI-negative controls NA Affymetrix [906600] 13 antiphospholipid antibody measurement http://www.ebi.ac.uk/efo/EFO_0005200 GCST001872 Genome-wide genotyping array 2012-08-10 22744181 Hai R 2012-06-29 Sci China Life Sci www.ncbi.nlm.nih.gov/pubmed/22744181 Bivariate genome-wide association study suggests that the DARC gene influences lean body mass and age at menarche. Lean body mass and age at menarche (combined) 801 Han Chinese ancestry female individuals 1,692 European ancestry female individuals Affymetrix [909622] 1 body fat distribution, age at menarche http://www.ebi.ac.uk/efo/EFO_0004341, http://www.ebi.ac.uk/efo/EFO_0004703 GCST001584 Genome-wide genotyping array 2011-06-16 21642993 Wu C 2011-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21642993 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. Esophageal cancer 2,031 Han Chinese ancestry cases, 2,044 Han Chinese ancestry controls 3,986 Han Chinese ancestry cases, 4,157 Han Chinese ancestry controls Affymetrix [666141] 11 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST001089 Genome-wide genotyping array 2011-06-23 21666692 Chasman DI 2011-06-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21666692 Genome-wide association study reveals three susceptibility loci for common migraine in the general population. Migraine 5,122 European ancestry cases, 18,108 European ancestry controls 3,831 European ancestry cases, 13,889 European ancestry controls Affymetrix, Illumina [2608509] (imputed) 3 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST001105 Genome-wide genotyping array 2013-09-27 23666238 Kou I 2013-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23666238 Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis. Scoliosis 1,033 Japanese ancestry cases, 1,473 Japanese ancestry controls 1,529 East Asian ancestry cases, 25,675 East Asian ancestry controls, 447 European ancestry cases, 737 European ancestry controls Illumina [465762] 2 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST002020 Genome-wide genotyping array 2013-09-20 23644492 Wu C 2013-05-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23644492 Genome-wide association study identifies common variants in SLC39A6 associated with length of survival in esophageal squamous-cell carcinoma. Esophageal squamous cell cancer (length of survival) 1,331 Chinese ancestry cases 1,062 Chinese ancestry individuals Affymetrix [665999] 1 survival time, squamous cell carcinoma, esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000707, http://www.ebi.ac.uk/efo/EFO_0002916 GCST002010 Genome-wide genotyping array 2012-03-30 22377092 Wang KS 2012-02-27 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/22377092 ANAPC1 and SLCO3A1 are associated with nicotine dependence: meta-analysis of genome-wide association studies. Nicotine dependence 1,079 European ancestry cases, 1,341 European ancestry controls 1,419 European ancestry cases, 1,885 European ancestry controls from 778 nuclear families Illumina [818866] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST001427 Genome-wide genotyping array 2011-06-18 21665988 Horne BD 2011-06-10 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/21665988 Genome-wide significance and replication of the chromosome 12p11.22 locus near the PTHLH gene for peripartum cardiomyopathy. Peripartum cardiomyopathy 36 European ancestry female cases, 703 European ancestry female controls, 5 female cases 59 European ancestry female cases, 303 European ancestry female controls Illumina [541327] 0 peripartum cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0002628 GCST001098 Genome-wide genotyping array 2011-12-03 22054870 De Jager PL 2011-11-03 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22054870 A genome-wide scan for common variants affecting the rate of age-related cognitive decline. Cognitive decline 749 European ancestry individuals 1,562 European ancestry individuals, 717 cases Affymetrix [672266] 1 psychomotor performance http://www.ebi.ac.uk/efo/EFO_0004362 GCST001311 Genome-wide genotyping array 2011-04-13 21428769 McCormack M 2011-03-24 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/21428769 HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans. Adverse response to carbamazepine 65 European ancestry cases, 3,987 European ancestry controls 80 European ancestry cases, 257 European ancestry controls Illumina [~ 1200000] (imputed) 1 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST001014 Genome-wide genotyping array 2010-03-17 20173748 Cho MH 2010-02-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20173748 Variants in FAM13A are associated with chronic obstructive pulmonary disease. Chronic obstructive pulmonary disease 2,940 European ancestry cases, 1,380 European ancestry controls 502 European ancestry cases, 504 European ancestry controls, 1,110 cases, 2,698 controls Illumina [499578] 3 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST000603 Genome-wide genotyping array 2013-04-17 23307926 Perry JR 2013-01-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23307926 A genome-wide association study of early menopause and the combined impact of identified variants. Menopause (age at onset) 3,493 European ancestry cases, 13,598 European ancestry controls 3,412 European ancestry cases, 4,928 European ancestry controls NR [NR] 8 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST001810 Genome-wide genotyping array 2012-01-27 22182935 Chen DT 2011-12-20 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22182935 Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder. Bipolar disorder 5,568 European ancestry cases, 7,187 European ancestry controls, 1,000 Taiwanese ancestry cases, 1,000 Taiwanese ancestry controls 1,115 European ancestry cases, 2,728 European ancestry controls Affymetrix, Illumina [748555] 5 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001358 Genome-wide genotyping array 2011-06-16 21626137 Slavin TP 2011-05-28 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21626137 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. Hypertension (SNP x SNP interaction) ~2,000 European ancestry cases, ~3,000 European ancestry controls NA Affymetrix [405022] 9 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST001085 Genome-wide genotyping array 2011-06-16 21626137 Slavin TP 2011-05-28 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21626137 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. Coronary heart disease (SNP X SNP interaction) ~2,000 European ancestry cases, ~3,000 European ancestry controls NA Affymetrix [407576] 5 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001084 Genome-wide genotyping array 2012-09-29 22883433 Irish Schizophrenia Genomics Consortium and the Wellcome Trust Case Control Consortium 2 2012-08-07 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22883433 Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia. Schizophrenia 1,606 European ancestry cases, 1,794 European ancestry controls 13,195 European ancestry cases, 31,021 European ancestry controls Affymetrix [6212339] 2 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001631 Genome-wide genotyping array 2011-12-16 22075330 Granada M 2011-11-08 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/22075330 A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study. IgE levels 6,819 European ancestry individuals 7,809 European ancestry indivduals Affymetrix [2540223] (imputed) 11 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST001316 Genome-wide genotyping array 2013-04-09 23251661 Comuzzie AG 2012-12-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/23251661 Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. Obesity-related traits 815 Hispanic children from 263 families NA Illumina [899892] 949 cortisol secretion measurement, hormone measurement, antioxidant measurement, CCL2 measurement, body mass index, IGFBP-3 measurement, fatty acid measurement, tumor necrosis factor-alpha measurement, gestational age, energy expenditure, sleep measurement, metabolic rate measurement, urinary metabolite measurement, blood urea nitrogen measurement, vitamin B12 measurement, energy intake, ICAM-1 measurement, body height, hip circumference, arm span, physical activity, heart rate, protein measurement, estradiol measurement, thyroid stimulating hormone measurement, waist circumference, total cholesterol measurement, interleukin-6 measurement, body composition measurement, birth weight, amino acid measurement, C-reactive protein measurement, HOMA-IR, head circumference, adiponectin measurement, high density lipoprotein cholesterol measurement, aspartate aminotransferase measurement, leptin measurement, transforming growth factor beta measurement, systolic blood pressure, IGFBP-1 measurement, bone density, body weight, fasting blood glucose measurement, homocysteine measurement, folic acid measurement, serum alanine aminotransferase measurement, CCL5 measurement, IGF-1 measurement, testosterone measurement, insulin sensitivity measurement, diastolic blood pressure, maximal oxygen uptake measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, lean body mass, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004642, http://www.ebi.ac.uk/efo/EFO_0004730, http://www.ebi.ac.uk/efo/EFO_0005119, http://www.ebi.ac.uk/efo/EFO_0004749, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004626, http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004684, http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0005109, http://www.ebi.ac.uk/efo/EFO_0004870, http://www.ebi.ac.uk/efo/EFO_0005115, http://www.ebi.ac.uk/efo/EFO_0005116, http://www.ebi.ac.uk/efo/EFO_0004741, http://www.ebi.ac.uk/efo/EFO_0004620, http://www.ebi.ac.uk/efo/EFO_0003939, http://www.ebi.ac.uk/efo/EFO_0004520, http://www.ebi.ac.uk/efo/EFO_0004339, http://www.ebi.ac.uk/efo/EFO_0005093, http://www.ebi.ac.uk/efo/EFO_0005108, http://www.ebi.ac.uk/efo/EFO_0003940, http://www.ebi.ac.uk/efo/EFO_0004326, http://www.ebi.ac.uk/efo/EFO_0004747, http://www.ebi.ac.uk/efo/EFO_0004697, http://www.ebi.ac.uk/efo/EFO_0004748, http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004810, http://www.ebi.ac.uk/efo/EFO_0005106, http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0005134, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0004501, http://www.ebi.ac.uk/efo/EFO_0005114, http://www.ebi.ac.uk/efo/EFO_0004502, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0004736, http://www.ebi.ac.uk/efo/EFO_0005000, http://www.ebi.ac.uk/efo/EFO_0004818, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005118, http://www.ebi.ac.uk/efo/EFO_0003923, http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004465, http://www.ebi.ac.uk/efo/EFO_0004578, http://www.ebi.ac.uk/efo/EFO_0005111, http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0005117, http://www.ebi.ac.uk/efo/EFO_0004627, http://www.ebi.ac.uk/efo/EFO_0004908, http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004887, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004995, http://www.ebi.ac.uk/efo/EFO_0004466 GCST001762 Genome-wide genotyping array 2012-10-09 22885925 Shi Y 2012-08-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22885925 Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome. Polycystic ovary syndrome 2,254 Han Chinese ancestry cases, 3,001 Han Chinese ancestry controls 8,226 Han Chinese ancestry cases, 7,578 Han Chinese ancestry controls Affymetrix [NR] (imputed) 11 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST001634 Genome-wide genotyping array 2013-07-01 23482656 Chen D 2013-03-12 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/23482656 Genome-wide association study of susceptibility loci for cervical cancer. Cervical cancer 1,034 European ancestry cases, 3,948 European ancestry controls 1,140 European ancestry cases, 1,058 European ancestry controls Illumina [632668] 6 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST001900 Genome-wide genotyping array 2015-05-14 22041458 Clark SL 2011-11-01 Psychol Med www.ncbi.nlm.nih.gov/pubmed/22041458 Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D. Response to anti-depressant treatment in major depressive disorder 1,151 European ancestry cases, 288 African American cases NA Affymetrix [421789] 22 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST001308 Genome-wide genotyping array 2014-03-01 23918034 Kuhnisch J 2013-08-07 Clin Oral Investig www.ncbi.nlm.nih.gov/pubmed/23918034 Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH). Molar-incisor hypomineralization 88 European ancestry cases, 580 European ancestry controls NA Affymetrix [2013491] (imputed) 5 molar-incisor hypomineralization http://www.ebi.ac.uk/efo/EFO_0005321 GCST002114 Genome-wide genotyping array 2011-11-24 22030708 Menke A 2011-10-26 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/22030708 Genome-wide association study of antidepressant treatment-emergent suicidal ideation. Suicidal ideation 397 European ancestry depressive disorder cases 501 European ancestry depressive disorder cases Illumina [371335] 0 lentiform nucleus measurement http://www.ebi.ac.uk/efo/EFO_0004913 GCST001296 Genome-wide genotyping array 2013-09-12 23535729 Michailidou K 2013-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23535729 Large-scale genotyping identifies 41 new loci associated with breast cancer risk. Breast cancer 10,052 European ancestry cases, 12,575 European ancestry controls 45,290 European ancestry cases, 41,880 European ancestry controls Affymetrix, Illumina [~ 2600000] (imputed) 63 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001937 Genome-wide genotyping array 2014-02-25 23910658 McRae JF 2013-07-31 Curr Biol www.ncbi.nlm.nih.gov/pubmed/23910658 Identification of regions associated with variation in sensitivity to food-related odors in the human genome. Odorant perception (isobutyraldehyde) 187 European ancestry individuals Up to 109 Asian ancestry indiviudals Affymetrix [619656] 1 sensory perception of smell http://purl.obolibrary.org/obo/GO_0007608 GCST002105 Genome-wide genotyping array 2014-02-21 23910658 McRae JF 2013-07-31 Curr Biol www.ncbi.nlm.nih.gov/pubmed/23910658 Identification of regions associated with variation in sensitivity to food-related odors in the human genome. Odorant perception (β-damascenone) 187 European ancestry individuals 89 European ancestry individuals Affymetrix [619656] 1 sensory perception of smell http://purl.obolibrary.org/obo/GO_0007608 GCST002106 Genome-wide genotyping array 2015-04-14 23910658 McRae JF 2013-07-31 Curr Biol www.ncbi.nlm.nih.gov/pubmed/23910658 Identification of regions associated with variation in sensitivity to food-related odors in the human genome. Odorant perception (β-ionone) 187 European ancestry individuals Up to 109 Asian ancestry individuals Affymetrix [619656] 1 sensory perception of smell http://purl.obolibrary.org/obo/GO_0007608 GCST002107 Genome-wide genotyping array 2011-06-25 21659334 Tanaka Y 2011-06-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21659334 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. Response to hepatitis C treatment 303 Japanese ancestry cases 391 Japanese ancestry cases Affymetrix [595052] 4 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST001094 Genome-wide genotyping array 2013-05-01 23326239 Rubicz R 2013-01-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23326239 A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1). Epstein-Barr virus immune response (EBNA-1) 1,367 Mexican American indivduals 589 Mexican American indivduals Illumina [944565] 2 antibody measurement, Epstein-Barr virus infection http://www.ebi.ac.uk/efo/EFO_0004556, http://www.ebi.ac.uk/efo/EFO_0000769 GCST001812 Genome-wide genotyping array 2013-06-01 23456168 Hao Y 2013-03-03 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23456168 Genome-wide association study in Han Chinese identifies three novel loci for human height. Height 6,534 Han Chinese ancestry individuals 1,881 Han Chinese ancestry individuals from 637 families Affymetrix [1532051] (imputed) 11 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST001885 Genome-wide genotyping array 2010-03-30 20222955 Pattaro C 2010-03-11 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/20222955 A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2 with serum creatinine level. Creatinine levels 4,006 European ancestry individuals 2,035 European ancestry individuals Illumina [~ 322498] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST000622 Genome-wide genotyping array 2013-12-07 23785401 Leone MA 2013-06-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/23785401 Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. Multiple sclerosis (OCB status) 49 European ancestry OCB negative cases, 513 European ancestry OCB positive cases 200 European ancestry OCB negative cases, 1684 European ancestry OCB positive cases Illumina [504967] 1 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST002072 Genome-wide genotyping array 2014-03-02 23900074 Pooley KA 2013-07-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23900074 A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk. Telomere length 2,240 European ancestry individuals 11,024 breast cancer cases, 15,065 controls Illumina, Perlegen [2448093] (imputed) 1 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST002103 Genome-wide genotyping array 2012-12-21 23054467 Postula M 2012-10-04 J Thromb Thrombolysis www.ncbi.nlm.nih.gov/pubmed/23054467 New single nucleotide polymorphisms associated with differences in platelets reactivity in patients with type 2 diabetes treated with acetylsalicylic acid: genome-wide association approach and pooled DNA strategy. Platelet reactivity 289 European ancestry type 2 diabetes cases treated with acetylsalicylic acid NA Illumina [200251] 0 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST001705 Genome-wide genotyping array 2012-11-22 23055271 Gregersen PK 2012-07-16 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/23055271 Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08. Myasthenia gravis 400 European ancestry cases, 5,505 European ancestry controls 249 European ancestry cases, 3,415 European ancestry controls Illumina [274256] 6 immune system disease http://www.ebi.ac.uk/efo/EFO_0000540 GCST001611 Genome-wide genotyping array 2013-03-19 23209189 Tabassum R 2012-12-03 Diabetes www.ncbi.nlm.nih.gov/pubmed/23209189 Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. Type 2 diabetes 1,101 Indo-European ancestry cases, 1,027 Indo-European ancestry controls 3,607 Indo-European ancestry cases, 2,924 Indo-European ancestry controls, 1,184 Dravidian ancestry cases, 1,061 Dravidian ancestry controls, 11,285 European ancestry cases, 11,285 European ancestry controls Illumina [536420] 6 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001759 Genome-wide genotyping array 2013-09-21 23650146 Tang W 2013-05-05 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/23650146 A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Venous thromboembolism 1,618 European ancestry cases, 42,881 European ancestry controls 3,231 European ancestry cases, 3,536 European ancestry controls Affymetrix, Illumina [2543885] (imputed) 8 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST002012 Genome-wide genotyping array 2012-04-06 22367438 Tao S 2012-02-26 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22367438 Genome-wide two-locus epistasis scans in prostate cancer using two European populations. Prostate cancer (SNP x SNP interaction) 1,176 cases, 1,101 controls 1,964 European ancestry cases, 3,172 European ancestry controls Illumina [509916] 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001426 Genome-wide genotyping array 2009-09-04 19680635 Alkelai A 2009-08-13 Psychopharmacology (Berl) www.ncbi.nlm.nih.gov/pubmed/19680635 Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients. Response to antipsychotic treatment 140 European ancestry cases, 117 European ancestry controls, 57 African American cases, 72 African American controls, 2 cases, 9 controls NA Affymetrix, Perlegen [495172] 1 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST000462 Genome-wide genotyping array 2009-08-12 19609347 Adeyemo A 2009-07-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19609347 A genome-wide association study of hypertension and blood pressure in African Americans. Hypertension 509 African American cases, 508 African American controls 366 West African ancestry cases, 614 West African ancestry controls Affymetrix [808465] 2 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST000447 Genome-wide genotyping array 2013-07-09 23535734 Codd V 2013-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23535734 Identification of seven loci affecting mean telomere length and their association with disease. Telomere length 37,684 European ancestry individuals 10,739 European ancestry individuals Affymetrix, Illumina [2362330] 3 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST001936 Genome-wide genotyping array 2014-04-04 23999434 Ho JE 2013-09-03 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/23999434 Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling. Serum protein levels (sST2) 2,797 individuals NA Affymetrix [2500000] (imputed) 14 serum ST2 measurement http://www.ebi.ac.uk/efo/EFO_0005416 GCST002166 Genome-wide genotyping array 2013-02-06 23146381 Levin AM 2012-11-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/23146381 A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations. IgE levels 2,469 African American individuals, 259 Latino individuals, 1,564 European ancestry individuals 2,961 African American individuals, 1,477 Latino individuals, 649 European ancestry individuals, 680 Hutterite individuals Affymetrix, Illumina [NR] (imputed) 4 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST001739 Genome-wide genotyping array 2012-06-19 22491018 Wang J 2012-04-10 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/22491018 Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis. Response to tocilizumab in rheumatoid arthritis 1,157 European and other ancestry rheumatoid arthritis cases 526 European and other ancestry rheumatoid arthritis cases Illumina [534053] 31 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST001476 Genome-wide genotyping array 2012-04-06 22417934 Athanasiu L 2012-03-12 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/22417934 Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study. Body mass index and cholesterol (psychopharmacological treatment) 283 European ancestry schizophrenia cases, 213 European ancestry bipolar disorder cases, 98 European ancestry psychosis cases NA Affymetrix [608239] 2 total cholesterol measurement, body mass index, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004340, http://purl.obolibrary.org/obo/GO_0009410 GCST001440 Genome-wide genotyping array 2012-05-02 22470424 Kwee LC 2012-03-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/22470424 A high-density genome-wide association screen of sporadic ALS in US veterans. Amyotrophic lateral sclerosis Up to 639 European ancestry cases, 6,257 European ancestry controls Up to 183 European ancestry cases, 961 European ancestry controls Affymetrix, Illumina [1280579] 2 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST001460 Genome-wide genotyping array 2010-08-17 20664687 Lin HJ 2010-07-01 Mol Vis www.ncbi.nlm.nih.gov/pubmed/20664687 Single-nucleotide polymorphisms in chromosome 3p14.1- 3p14.2 are associated with susceptibility of type 2 diabetes with cataract. Cataracts in type 2 diabetes 109 Han Chinese ancestry cases, 649 Han Chinese ancestry controls NA Illumina [517401] 0 diabetes mellitus type 2 associated cataract http://www.ebi.ac.uk/efo/EFO_0004596 GCST000717 Genome-wide genotyping array 2011-09-21 21829393 Plagnol V 2011-08-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829393 Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. Type 1 diabetes 8,506 European ancestry cases, up to 10,596 European ancestry controls NA Affymetrix, Illumina [NR] 22 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST001191 Genome-wide genotyping array 2017-07-24 21829393 Plagnol V 2011-08-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829393 Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. Glutamate decarboxylase autoantibody levels in type 1 diabetes 2,506 European ancestry cases NA Affymetrix, Illumina [NR] 0 autoantibody measurement http://www.ebi.ac.uk/efo/EFO_0004866 GCST004380 Genome-wide genotyping array 2017-07-24 21829393 Plagnol V 2011-08-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829393 Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. Insulinoma-associated antigen 2 autoantibody levels in type 1 diabetes 2,498 European ancestry cases 3,897 sibling cases Affymetrix, Illumina [NR] 1 autoantibody measurement http://www.ebi.ac.uk/efo/EFO_0004866 GCST004381 Genome-wide genotyping array 2017-07-24 21829393 Plagnol V 2011-08-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829393 Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. Gastric parietal cell autoantibody levels in type 1 diabetes 4,328 European ancestry cases NA Affymetrix, Illumina [NR] 1 autoantibody measurement http://www.ebi.ac.uk/efo/EFO_0004866 GCST004382 Genome-wide genotyping array 2017-07-24 21829393 Plagnol V 2011-08-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829393 Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases. Thyroid peroxidase autoantibody levels in type 1 diabetes 8,300 European ancestry cases NA Affymetrix, Illumina [NR] 1 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST004383 Genome-wide genotyping array 2009-07-12 19567438 Elliott P 2009-07-01 JAMA www.ncbi.nlm.nih.gov/pubmed/19567438 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. C-reactive protein 17,967 European ancestry and Indian Asian ancestry individuals 13,615 European ancestry and Indian Asian ancestry Individuals Affymetrix, Illumina, Perlegen [~ 1400000] (imputed) 5 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST000430 Genome-wide genotyping array 2012-04-28 22497812 Clark PJ 2012-02-22 J Viral Hepat www.ncbi.nlm.nih.gov/pubmed/22497812 Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response. Lipid levels in hepatitis C treatment 1,017 European ancestry cases, 207 African American cases, 95 Hispanic cases NA Illumina [565759] 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST001418 Genome-wide genotyping array 2013-10-18 20152958 Xing C 2010-02-11 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20152958 A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels. Fasting plasma glucose 2,029 African American individuals, 7,428 European ancestry individuals 1,571 African American individuals, 3,825 European ancestry individuals Affymetrix [814004] 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000591 Genome-wide genotyping array 2011-06-25 21659360 Wade R 2011-06-09 Haematologica www.ncbi.nlm.nih.gov/pubmed/21659360 Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial. Response to antineoplastic agents 356 European ancestry cases 380 European ancestry cases Illumina [326385] 9 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST001095 Genome-wide genotyping array 2012-12-11 23028342 Sandholm N 2012-09-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23028342 New susceptibility loci associated with kidney disease in type 1 diabetes. Type 1 diabetes nephropathy Up to 2,916 European ancestry Type 1 Diabetes cases with nephropathy, 3,315 European ancestry Type 1 Diabetes cases without nephropathy Up to 1,493 European ancestry Type 1 Diabetes cases with nephropathy, 3,191 European ancestry Type 1 Diabetes cases without nephropathy Affymetrix, Illumina [~ 2500000] (imputed) 11 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST001688 Genome-wide genotyping array 2013-06-13 23472185 Mero IL 2013-03-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/23472185 Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. Multiple sclerosis (OCB status) 1,367 European ancestry OCB positive cases, 161 European ancestry OCB negative cases, 428 European ancestry controls NA Illumina [495970] 8 oligoclonal band measurement, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0005206, http://purl.obolibrary.org/obo/MONDO_0005301 GCST001892 Genome-wide genotyping array 2013-06-13 23472185 Mero IL 2013-03-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/23472185 Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. Multiple sclerosis (OCB status) 1,367 European ancestry OCB positive cases, 161 European ancestry OCB negative cases 3,029 European ancestry OCB positive cases, 374 European ancestry OCB negative cases Illumina [495970] 3 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST001891 Genome-wide genotyping array 2013-06-13 23463857 Ritchie MD 2013-03-05 Circulation www.ncbi.nlm.nih.gov/pubmed/23463857 Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk. Electrocardiographic conduction measures 5,272 European ancestry indiviudals 40,407 European ancestry individuals Illumina [528508] 5 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST001893 Genome-wide genotyping array 2008-10-14 18762592 van den Oord EJ 2008-09-01 Arch Gen Psychiatry www.ncbi.nlm.nih.gov/pubmed/18762592 Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism. Neuroticism 1,227 European ancestry individuals 1,880 European ancestry individuals Affymetrix [420287] 3 neurotic disorder http://www.ebi.ac.uk/efo/EFO_0004257 GCST000226 Genome-wide genotyping array 2013-06-04 23432519 O'Brien RP 2013-02-21 Clin Transplant www.ncbi.nlm.nih.gov/pubmed/23432519 A genome-wide association study of recipient genotype and medium-term kidney allograft function. Renal transplant outcome 263 European ancestry individuals Illumina [511662] 4 renal transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005199 GCST001871 Genome-wide genotyping array 2014-08-08 24047446 Schosser A 2013-09-19 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24047446 Genome-wide association study of co-occurring anxiety in major depression. Anxiety in major depressive disorder 1,080 European ancestry cases, 442 European ancestry controls NA Illumina [471581] 8 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST002202 Genome-wide genotyping array 2014-08-08 24047446 Schosser A 2013-09-19 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24047446 Genome-wide association study of co-occurring anxiety in major depression. Anxiety and major depressive disorder 1,080 European ancestry cases, 1,588 European ancestry controls NA Illumina [471581] 3 unipolar depression, anxiety http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0005230 GCST002200 Genome-wide genotyping array 2008-11-12 18836448 Franke A 2008-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18836448 Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility. Ulcerative colitis 1,167 European ancestry cases, 777 European ancestry controls 1,855 European ancestry cases, 3,091 European ancestry controls Affymetrix [355262] 2 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000243 Genome-wide genotyping array 2011-12-17 22085899 Chen G 2011-11-16 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22085899 UGT1A1 is a major locus influencing bilirubin levels in African Americans. Bilirubin levels 619 African American individuals NA Affymetrix [808465] 9 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST001324 Genome-wide genotyping array 2011-11-25 22021425 Carty CL 2011-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22021425 Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe). Height 8,149 African American female individuals Up to 20,809 African American and African ancestry individuals Affymetrix [855034] 8 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST001290 Genome-wide genotyping array 2011-12-21 22131368 Chen CT 2011-11-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22131368 Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study. Menarche and menopause (age at onset) 3,468 Hispanic female individuals NA Affymetrix [871309] 0 age at menarche, age at menopause http://www.ebi.ac.uk/efo/EFO_0004703, http://www.ebi.ac.uk/efo/EFO_0004704 GCST001336 Genome-wide genotyping array 2013-06-06 23453885 Smoller JW 2013-02-27 Lancet www.ncbi.nlm.nih.gov/pubmed/23453885 Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis. Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined) 6,990 European ancestry Bipolar disorder cases, 9,227 European ancestry Major depressive disorder cases, 9,379 European ancestry Schizophrenia cases, 161 European ancestry Autism spectrum disorder cases, 4,788 European ancestry Autism spectrum disorder trio cases, 840 European ancestry Attention deficit-hyperactivity disorder cases, 1,947 European ancestry Attention defcit-hyperactivity disorder trio cases, 27,888 European ancestry controls NA NR [1252901] (imputed) 74 attention deficit hyperactivity disorder, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090 GCST001877 Genome-wide genotyping array 2008-12-01 18980221 Neale BM 2008-11-03 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18980221 Genome-wide association scan of attention deficit hyperactivity disorder. Attention deficit hyperactivity disorder 909 European ancestry trios NA Perlegen [438784] 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST000259 Genome-wide genotyping array 2012-04-24 22479419 Liou YJ 2012-03-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/22479419 Genome-wide association study of treatment refractory schizophrenia in Han Chinese. Schizophrenia (treatment resistant) 522 Han Chinese ancestry cases, 806 Han Chinese ancestry controls 273 Han Chinese ancestry cases Affymetrix [694436] 2 treatment refractory schizophrenia http://www.ebi.ac.uk/efo/EFO_0004609 GCST001458 Genome-wide genotyping array 2013-01-16 23133572 Rye MS 2012-10-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/23133572 Genome-wide association study to identify the genetic determinants of otitis media susceptibility in childhood. Otitis media (chronic/recurrent) 416 cases and 1,075 controls of European and unknown ancestry 1,941 European and unknown ancestry individuals, 142 individuals from 645 families Illumina [2509905] (imputed) 0 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST001717 Genome-wide genotyping array 2012-06-02 22504421 Bis JC 2012-04-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22504421 Common variants at 12q14 and 12q24 are associated with hippocampal volume. Hippocampal volume 9,232 European ancestry individuals 2,318 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 5 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST001485 Genome-wide genotyping array 2010-12-09 21118971 Wu C 2010-11-30 Cancer Res www.ncbi.nlm.nih.gov/pubmed/21118971 Genome-wide interrogation identifies YAP1 variants associated with survival of small-cell lung cancer patients. Small-cell lung cancer (survival) 245 Han Chinese ancestry cases 305 Han Chinese ancestry cases Affymetrix [265996] 1 small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000702 GCST000896 Genome-wide genotyping array 2012-03-08 22318345 Cha PC 2012-02-09 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22318345 A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population. Gallbladder cancer 41 Japanese ancestry cases, 866 Japanese ancestry controls 30 Japanese ancestry cases, 898 Japanese ancestry controls Illumina [425706] (imputed) 5 gallbladder neoplasm http://www.ebi.ac.uk/efo/EFO_0004606 GCST001404 Genome-wide genotyping array 2012-09-11 22792070 Medina-Gomez C 2012-07-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22792070 Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus. Bone mineral density 1,834 European ancestry children, 825 children 11,052 European ancestry individuals Illumina [3021329] (imputed) 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST001594 Genome-wide genotyping array 2011-01-08 21104366 Tan L 2010-11-23 Sci China Life Sci www.ncbi.nlm.nih.gov/pubmed/21104366 A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass. Bone mineral density (wrist) 1,000 European ancestry individuals 1,628 Chinese ancestry individuals Affymetrix [379319] 1 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST000881 Genome-wide genotyping array 2011-01-04 21094521 Wan YI 2010-11-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/21094521 A genome-wide association study to identify genetic determinants of atopy in subjects from the United Kingdom. Atopy 1,083 European ancestry cases, 2,770 European ancestry controls Up to 1,058 European ancestry cases, 2,254 European ancestry controls Illumina [459334] 0 atopy http://www.ebi.ac.uk/efo/EFO_0002686 GCST000870 Genome-wide genotyping array 2010-12-03 20966902 Croteau-Chonka DC 2010-10-21 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/20966902 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. Weight 1,780 Filipino ancestry females NA Affymetrix [2073674] (imputed) 7 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST000837 Genome-wide genotyping array 2010-12-03 20966902 Croteau-Chonka DC 2010-10-21 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/20966902 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. Waist circumference 1,779 Filipino ancestry females NA Affymetrix [2073674] (imputed) 8 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST000838 Genome-wide genotyping array 2010-12-03 20966902 Croteau-Chonka DC 2010-10-21 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/20966902 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. Body mass index 1,780 Filipino ancestry females NA Affymetrix [2073674] (imputed) 6 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000840 Genome-wide genotyping array 2010-12-03 20966902 Croteau-Chonka DC 2010-10-21 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/20966902 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. Height 1,792 Filipino ancestry females NA Affymetrix [2073674] (imputed) 7 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000839 Genome-wide genotyping array 2011-07-29 21750702 Schosser A 2011-07-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/21750702 Genomewide association scan of suicidal thoughts and behaviour in major depression. Suicidal ideation 2,023 European ancestry major depressive disorder cases 1,531 European ancestry major depressive disorder cases Illumina [532774] 0 lentiform nucleus measurement http://www.ebi.ac.uk/efo/EFO_0004913 GCST001141 Genome-wide genotyping array 2011-01-14 21087763 Carrasquillo MM 2010-12-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21087763 Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma. Progranulin levels 518 European ancestry controls 459 European ancestry controls Illumina [313504] 1 progranulin measurement http://www.ebi.ac.uk/efo/EFO_0004625 GCST000911 Genome-wide genotyping array 2012-05-25 22509378 Burri A 2012-04-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/22509378 A genome-wide association study of female sexual dysfunction. Sexual dysfunction (female) 1,104 European ancestry twins NA Illumina [2287762] (imputed) 3 sexual dysfunction http://www.ebi.ac.uk/efo/EFO_0004714 GCST001477 Genome-wide genotyping array 2012-04-27 22446963 Okada Y 2012-03-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22446963 Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population. Rheumatoid arthritis 4,074 Japanese ancestry cases, 16,891 Japanese ancestry controls 5,277 Japanese ancestry cases, 21,684 Japanese ancestry controls Affymetrix, Illumina [1948139] 15 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST001454 Genome-wide genotyping array 2011-08-18 21799836 Cui B 2011-07-22 PLoS One www.ncbi.nlm.nih.gov/pubmed/21799836 A genome-wide association study confirms previously reported loci for type 2 diabetes in Han Chinese. Type 2 diabetes 793 Han Chinese ancestry cases, 806 Han Chinese ancestry controls 4,445 Han Chinese ancestry cases, 4,458 Han Chinese ancestry controls Illumina [474515] 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001173 Genome-wide genotyping array 2012-03-03 22322875 Kim SJ 2012-02-09 Circ J www.ncbi.nlm.nih.gov/pubmed/22322875 Genetic association of short sleep duration with hypertension incidence--a 6-year follow-up in the Korean genome and epidemiology study. Hypertension risk in short sleep duration 4,965 Korean ancestry individuals NA Affymetrix [334750] 3 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST001405 Genome-wide genotyping array 2008-06-27 18451265 Bouatia-Naji N 2008-06-19 Science www.ncbi.nlm.nih.gov/pubmed/18451265 A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels. Fasting plasma glucose 654 European ancestry individuals 9,353 European ancestry individuals Illumina [392935] 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000205 Genome-wide genotyping array 2008-06-16 17999355 Stokowski RP 2007-10-15 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/17999355 A genomewide association study of skin pigmentation in a South Asian population. Skin pigmentation 363 South Asian ancestry low maxL* individuals, 374 South Asian ancestry high maxL* individuals 116 South Asian ancestry low maxL* individuals, 115 South Asian ancestry high maxL* individuals Perlegen [1502205] 3 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST000114 Genome-wide genotyping array 2011-07-27 21738479 Reiner AP 2011-06-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21738479 Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT). White blood cell count 16,388 African American individuals 3,551 Hispanic individuals, 14,767 Japanese ancestry individuals, 19,509 European ancestry individuals Affymetrix, Illumina [2489215] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST001133 Genome-wide genotyping array 2013-09-18 23593239 van der Loos MJ 2013-04-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/23593239 The molecular genetic architecture of self-employment. Self-employment 7,734 European ancestry cases, 42,893 European ancestry controls 737 cases, 2,534 controls Affymetrix, Illumina [~ 2400000] (imputed) 2 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST001952 Genome-wide genotyping array 2013-02-27 23237013 Power RA 2012-12-14 Psychol Med www.ncbi.nlm.nih.gov/pubmed/23237013 Estimating the heritability of reporting stressful life events captured by common genetic variants. Reporting of stressful life event 2,578 European ancestry depression cases and controls 864 European ancestry depression cases, 257 European ancestry controls Illumina [541628] 0 self rated health, stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0004778, http://www.ebi.ac.uk/efo/EFO_0007781 GCST001774 Genome-wide genotyping array 2011-01-08 21098978 Sherva R 2010-11-25 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/21098978 Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP data. Alzheimer's disease 124 Isreali Arab cases, 142 Israeli Arab controls 1,930 European ancestry cases, 1,312 European ancestry controls, 931 European ancestry and Ashkenazi Jewish cases, 1,104 European ancestry and Ashkenazi Jewish controls Illumina [~ 300000] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000886 Genome-wide genotyping array 2011-12-02 22051697 Du R 2011-11-01 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/22051697 Genome-wide association study reveals class I MHC-restricted T cell-associated molecule gene (CRTAM) variants interact with vitamin D levels to affect asthma exacerbations. Asthma 395 European ancestry child cases 584 Hispanic child cases Illumina [534290] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001309 Genome-wide genotyping array 2011-12-15 22072270 Wang KS 2011-11-11 J Neural Transm (Vienna) www.ncbi.nlm.nih.gov/pubmed/22072270 Genome-wide association study identifies 5q21 and 9p24.1 (KDM4C) loci associated with alcohol withdrawal symptoms. Alcohol withdrawal symptoms 461 European ancestry cases, 408 European ancestry controls 318 European ancestry cases, 507 European ancestry controls Illumina [778974] 0 alcohol withdrawal http://www.ebi.ac.uk/efo/EFO_0004777 GCST001319 Genome-wide genotyping array 2012-10-16 22864933 O'Donnell PH 2012-01-03 Cancer www.ncbi.nlm.nih.gov/pubmed/22864933 Identification of novel germline polymorphisms governing capecitabine sensitivity. Capecitabine sensitivity Up to 84 East Asian ancestry lymphoblastoid cell lines, up to 164 European ancestry lymphoblastoid cell lines, up to 173 African ancestry lymphoblastoid cell lines, up to 82 African American lymphoblastoid cell lines NA NR [~ 2000000] 22 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST001368 Genome-wide genotyping array 2008-12-09 18957941 Terracciano A 2008-11-24 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/18957941 Genome-wide association scan for five major dimensions of personality. Personality dimensions 3,972 Sardinian individuals 3,903 individuals Affymetrix [362129] 5 personality trait http://www.ebi.ac.uk/efo/EFO_0004365 GCST000273 Genome-wide genotyping array 2011-08-12 21757653 Lovely RS 2011-07-14 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/21757653 Assessment of genetic determinants of the association of γ' fibrinogen in relation to cardiovascular disease. Fibrinogen 3,042 individuals NA Affymetrix [~ 2500000] (imputed) 5 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST001158 Genome-wide genotyping array 2011-09-08 21799462 Srinivasan Y 2011-07-27 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/21799462 Genome-wide association study of epirubicin-induced leukopenia in Japanese patients. Epirubicin-induced leukopenia 67 Japanese ancestry cases, 203 Japanese ancestry controls 48 Japanese ancestry cases Illumina [478359] 2 leukopenia http://www.ebi.ac.uk/efo/EFO_0004233 GCST001175 Genome-wide genotyping array 2013-06-06 23420232 Duggal P 2013-02-19 Ann Intern Med www.ncbi.nlm.nih.gov/pubmed/23420232 Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts. Chronic hepatitis C infection 1,482 chronic HCV cases, 919 spontaneously cleared HCV cases 461 chronic HCV cases, 284 spontaneously cleared HCV cases Illumina [792721] (imputed) 2 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST001867 Genome-wide genotyping array 2013-05-09 23378610 Xie W 2013-02-01 Diabetes www.ncbi.nlm.nih.gov/pubmed/23378610 Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes. Metabolite levels 1,004 European ancestry individuals 339 European ancestry individuals Affymetrix [909508] (imputed) 6 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST001852 Genome-wide genotyping array 2013-09-21 23667675 Tanikawa C 2013-05-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/23667675 Genome wide association study of age at menarche in the Japanese population. Menarche (age at onset) 15,495 Japanese ancestry females NA Illumina [2310762] (imputed) 8 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST002013 Genome-wide genotyping array 2015-05-20 21801394 Genin E 2011-07-29 Orphanet J Rare Dis www.ncbi.nlm.nih.gov/pubmed/21801394 Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe. Drug-induced Stevens-Johnson syndrome or toxic epidermal necrolysis (SJS/TEN) 424 European ancestry cases, 1,881 European ancestry controls NA Illumina [268914] 6 Stevens-Johnson syndrome, toxic epidermal necrolysis http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775 GCST001181 Genome-wide genotyping array 2013-08-28 23599027 Demerath EW 2013-04-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23599027 Genome-wide association study of age at menarche in African-American women. Menarche (age at onset) 18,089 African American individuals 2,850 African American individuals, 87,802 European ancestry inidividuals Affymetrix, Illumina [NR] (imputed) 15 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST001973 Genome-wide genotyping array 2008-12-09 18978790 McKay JD 2008-11-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18978790 Lung cancer susceptibility locus at 5p15.33. Lung cancer 2,971 European ancestry cases, 3,746 European ancestry controls 2,899 European ancestry cases, 5,573 European ancestry controls Illumina [315194] 2 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000256 Genome-wide genotyping array 2013-05-14 23408906 Porcu E 2013-02-07 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23408906 A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function. Thyroid hormone levels up to 14,459 European ancestry females, up to 10,936 European ancestry males, up to 433 Old Order Amish females, up to 592 Old Order Amish males NA Affymetrix, Illumina [~ 2500000] (imputed) 60 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST001856 Genome-wide genotyping array 2012-04-25 22443383 Oudot-Mellakh T 2012-01-16 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/22443383 Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. Hemostatic factors and hematological phenotypes 951 European ancestry individuals NA Illumina [472123] 9 hematological measurement http://www.ebi.ac.uk/efo/EFO_0004503 GCST001378 Genome-wide genotyping array 2015-05-06 22791750 Chen G 2012-07-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22791750 Genome-wide association study identifies novel loci association with fasting insulin and insulin resistance in African Americans. Insulin-related traits 927 African American non-diabetic individuals 570 West African ancestry non-diabetic individuals Affymetrix [5396838] (imputed) 6 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST001604 Genome-wide genotyping array 2012-04-18 22437316 Sarig O 2012-03-22 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/22437316 Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris. Pemphigus vulgaris 100 Jewish cases, 397 Jewish controls 59 Jewish cases, 285 Jewish controls, 124 European ancestry cases, 275 European anestry controls, 126 North African ancestry controls, 246 North African ancestry controls Illumina [293635] 0 pemphigus vulgaris http://www.ebi.ac.uk/efo/EFO_0004719 GCST001452 Genome-wide genotyping array 2013-05-14 23393555 Jensen RA 2013-02-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/23393555 Genome-wide association study of retinopathy in individuals without diabetes. Retinopathy in non-diabetics 19,411 European ancestry individuals NA Illumina [2675979] (imputed) 11 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST001854 Genome-wide genotyping array 2011-01-07 21095009 Li YJ 2010-11-20 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/21095009 Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. Myopia (pathological) 65 Singaporean Chinese child cases, 238 Singaporean Chinese child controls, 222 Singaporean Chinese adult cases, 455 Singaporean Chinese adult cases 959 Japanese ancestry cases, 2,128 Japanese ancestry controls Illumina [459687] 1 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST000878 Genome-wide genotyping array 2013-07-05 23535911 Kitamoto T 2013-03-28 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23535911 Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan. Pediatric non-alcoholic fatty liver disease activity score 392 Japanese ancestry cases, 934 Japanese ancestry controls 172 Japanese ancestry cases, 1,012 Japanese ancestry controls Illumina [261540] 4 non-alcoholic fatty liver disease, cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0003095, http://www.ebi.ac.uk/efo/EFO_0001422 GCST001928 Genome-wide genotyping array 2012-09-20 22788528 Kong M 2012-07-13 Int J Immunogenet www.ncbi.nlm.nih.gov/pubmed/22788528 Genetic associations with C-reactive protein level and white blood cell count in the KARE study. C-reactive protein and white blood cell count 8,722 individuals NA Affymetrix [1701735] (imputed) 9 leukocyte count, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004308, http://www.ebi.ac.uk/efo/EFO_0004458 GCST001605 Genome-wide genotyping array 2013-02-08 23180272 Park BL 2012-11-21 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23180272 Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population. Aspirin exacerbated respiratory disease in asthmatics 117 Korean ancestry cases, 685 Korean ancestry controls 142 Korean ancestry cases, 996 Korean ancestry controls Illumina [430486] 1 Aspirin-induced asthma http://purl.obolibrary.org/obo/HP_0012042 GCST001747 Genome-wide genotyping array 2011-06-14 21621269 Aragam N 2011-05-26 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/21621269 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. Major depressive disorder 1,726 cases, 1,630 controls NA Perlegen [433556] 5 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST001083 Genome-wide genotyping array 2011-10-07 21912425 Tohkin M 2011-09-13 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/21912425 A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients. Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN) 14 Japanese ancestry cases, 991 Japanese ancestry controls NA Illumina [890321] 1 Stevens-Johnson syndrome, toxic epidermal necrolysis http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775 GCST001239 Genome-wide genotyping array 2013-06-26 23535033 Sherva R 2013-03-24 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/23535033 Genome-wide association study of the rate of cognitive decline in Alzheimer's disease. Alzheimer's disease (cognitive decline) 303 European ancestry cases Illumina [NR] (imputed) 44 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001915 Genome-wide genotyping array 2011-06-14 21625490 Andiappan AK 2011-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/21625490 Genome-wide association study for atopy and allergic rhinitis in a Singapore Chinese population. Atopy 515 Chinese ancestry cases, 486 Chinese ancestry controls 2,323 Chinese ancestry cases, 511 Chinese ancestry controls Illumina [460183] 0 atopy http://www.ebi.ac.uk/efo/EFO_0002686 GCST001075 Genome-wide genotyping array 2013-01-25 23144319 Lee Y 2012-11-08 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/23144319 Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study. Non-small cell lung cancer 348 Korean ancestry cases NA Affymetrix [271817] 13 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST001734 Genome-wide genotyping array 2011-06-17 21640322 Shi Y 2011-06-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21640322 Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. Myopia (pathological) 419 Han Chinese ancestry high myopia cases, 669 Han Chinese ancestry controls 2,803 East Asian ancestry high myopia cases, 5,642 East Asian ancestry controls Illumina [493947] 1 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST001088 Genome-wide genotyping array 2012-09-12 22792082 Himes BE 2012-07-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22792082 Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene. Asthma (bronchodilator response) 1,644 European ancestry cases 1,051 European ancestry cases Affymetrix, Illumina [4571615] (imputed) 1 response to bronchodilator http://purl.obolibrary.org/obo/GO_0097366 GCST001597 Genome-wide genotyping array 2013-05-02 23374588 Martinelli-Boneschi F 2013-01-29 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/23374588 Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors. Response to cholinesterase inhibitors in Alzheimer's disease 92 European ancestry cases, 77 European ancestry controls 94 European ancestry cases, 74 European ancestry controls Illumina [522109] 3 response to cholinesterase inhibitor http://www.ebi.ac.uk/efo/EFO_0005195 GCST001835 Genome-wide genotyping array 2014-04-16 24162737 Lambert JC 2013-10-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24162737 Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. Alzheimer's disease (late onset) 17,008 European ancestry cases, 37,154 European ancestry controls 8,572 European ancestry cases, 11,312 European ancestry controls Illumina [7055881] (imputed) 33 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002245 Genome-wide genotyping array 2011-12-15 22080838 Cho MH 2011-11-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22080838 A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. Chronic obstructive pulmonary disease 3,499 European ancestry cases, 1,922 European ancestry controls 983 cases, 1,876 sibling controls Illumina [797983] 4 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST001321 Genome-wide genotyping array 2014-03-13 23918589 Negi S 2013-12-01 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/23918589 A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians. Rheumatoid arthritis 706 North Indian ancestry cases, 761 North Indian ancestry controls 927 North Indian ancestry cases, 1,148 North Indian ancestry controls Illumina [559348] 2 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST002300 Genome-wide genotyping array 2013-11-03 20350937 Takahashi M 2010-03-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20350937 The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl. Thyroid cancer (Papillary, radiation-related) 401 European ancestry cases, 620 European ancestry controls 259 cases, 648 controls Illumina [506840] 1 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST000640 Genome-wide genotyping array 2013-01-18 23139255 Butler AM 2012-11-08 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23139255 Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts. PR interval 13,415 African American individuals NA Affymetrix, Illumina [2845108] (imputed) 8 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST001735 Genome-wide genotyping array 2009-12-11 19915572 Barrett JC 2009-11-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19915572 Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region. Ulcerative colitis 2,361 European ancestry cases, 5,417 European ancestry controls 2,321 European ancestry cases, 4,818 European ancestry controls Affymetrix [NR] 13 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000527 Genome-wide genotyping array 2011-05-27 21533024 Pare G 2011-04-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21533024 Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci. Soluble ICAM-1 22,435 European ancestry female individuals 9,813 individuals Illumina [334295] 3 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST001047 Genome-wide genotyping array 2012-06-18 22437554 Major JM 2012-03-21 J Nutr www.ncbi.nlm.nih.gov/pubmed/22437554 Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men. Response to Vitamin E supplementation 2,112 European ancestry individuals NA Illumina [549989] 8 response to vitamin http://purl.obolibrary.org/obo/GO_0033273 GCST001450 Genome-wide genotyping array 2013-04-30 23480133 Kim Y 2011-02-28 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23480133 Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia. Vascular dementia 84 Korean ancestry cases, 200 Korean ancestry controls 113 Korean ancestry cases, 255 Korean ancestry controls NR [300640] 1 GCST000993 Genome-wide genotyping array 2012-06-21 22504417 Stein JL 2012-04-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22504417 Identification of common variants associated with human hippocampal and intracranial volumes. Brain structure 2,020 European ancestry neuropsychiatric disorder cases, 5,775 European ancestry controls 599 European ancestry neuropsychiatric disorder cases, 11,915 European ancestry controls, 143 European ancestry and African American neuropsychiatric disorder cases, 94 European ancestry and African American controls, 605 Hispanic controls Affymetrix, Illumina [NR] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST001481 Genome-wide genotyping array 2013-06-06 23396134 Verhoeven VJ 2013-02-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23396134 Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Refractive error 37,382 European ancestry individuals, 3,995 Chinese ancestry individuals, 2,273 Malay ancestry individuals, 2,108 Indian ancestry individuals NA Affymetrix, Illumina [2500000] (imputed) 26 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST001858 Genome-wide genotyping array 2012-05-15 22488850 Zuo L 2012-04-04 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/22488850 Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. Alcohol and nicotine co-dependence 818 European ancestry cases, 1,396 European ancestry controls, 449 African American cases, 480 African American controls NA Illumina [805814] 8 alcohol and nicotine codependence http://www.ebi.ac.uk/efo/EFO_0004776 GCST001471 Genome-wide genotyping array 2012-05-11 22492993 Doumatey AP 2012-04-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22492993 C-reactive protein (CRP) promoter polymorphisms influence circulating CRP levels in a genome-wide association study of African Americans. C-reactive protein 837 African American individuals 486 West African ancestry individuals Affymetrix [2366856] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST001472 Genome-wide genotyping array 2013-04-11 22504420 Estrada K 2012-04-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22504420 Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Lumbar spine bone mineral density Up to 32,961 European and East Asian ancestry individuals Up to 50,933 European and East Asian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 34 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST001482 Genome-wide genotyping array 2019-05-01 22504420 Estrada K 2012-04-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22504420 Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Femoral neck bone mineral density Up to 32,961 European and East Asian ancestry individuals Up to 50,933 European and East Asian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 35 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST007691 Genome-wide genotyping array 2012-05-11 22472876 Sullivan PF 2012-04-03 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22472876 A mega-analysis of genome-wide association studies for major depressive disorder. Major depressive disorder 9,240 European ancestry cases, 9,519 European ancestry controls 6,783 European ancestry cases, 50,695 European ancestry controls Affymetrix, Illumina, Perlegen [~ 1200000] (imputed) 5 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST001469 Genome-wide genotyping array 2012-06-01 22504418 Ikram MA 2012-04-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22504418 Common variants at 6q22 and 17q21 are associated with intracranial volume. Intracranial volume 8,175 European ancestry individuals 1,752 European ancestry individuals Affymetrix, Illumina [2229753] (imputed) 2 intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0004886 GCST001483 Genome-wide genotyping array 2013-09-12 23624525 Deng M 2013-04-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23624525 Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 506 Han Chinese ancestry cases, 1,859 Han Chinese ancestry controls 706 Han Chinese ancestry cases, 1,777 Han Chinese ancestry controls Illumina [473683] 2 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST001981 Genome-wide genotyping array 2010-10-14 20861866 Kopplin LJ 2010-09-23 Genes Immun www.ncbi.nlm.nih.gov/pubmed/20861866 Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. Age-related macular degeneration 684 European ancestry cases, 188 European ancestry controls 1,896 European ancestry cases, 1,866 European ancestry controls Affymetrix [> 361556] (imputed) 4 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST000806 Genome-wide genotyping array 2010-12-09 21060860 Gaudet MM 2010-10-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21060860 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. Breast cancer in BRCA2 mutation carriers 899 European ancestry cases, 804 European ancestry controls 1,264 European ancestry cases, 1,222 European ancestry controls Affymetrix [592163] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000846 Genome-wide genotyping array 2011-04-07 21372407 Takeuchi F 2011-03-01 Circ J www.ncbi.nlm.nih.gov/pubmed/21372407 Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population. Drinking behavior 733 Japanese ancestry cases, 729 Japanese ancestry controls 2,794 Japanese ancestry drinkers, 1,521 Japanese ancestry chance drinkers, 1,351 Japanese ancestry non-drinkers Illumina [456827] 2 drinking behavior http://www.ebi.ac.uk/efo/EFO_0004315 GCST000994 Genome-wide genotyping array 2012-08-14 22566634 Benjamin DJ 2012-05-07 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22566634 The genetic architecture of economic and political preferences. Economic and political preferences 9,617 European ancestry individuals NA Illumina [628922] 17 economic and social preference http://www.ebi.ac.uk/efo/EFO_0004827 GCST001519 Genome-wide genotyping array 2012-08-14 22566634 Benjamin DJ 2012-05-07 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22566634 The genetic architecture of economic and political preferences. Economic and political preferences (environmentalism) 9,617 European ancestry individuals NA Illumina [628922] 17 economic and social preference http://www.ebi.ac.uk/efo/EFO_0004827 GCST001512 Genome-wide genotyping array 2012-08-14 22566634 Benjamin DJ 2012-05-07 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22566634 The genetic architecture of economic and political preferences. Economic and political preferences (fairness) 9,617 European ancestry individuals NA Illumina [628922] 7 economic and social preference http://www.ebi.ac.uk/efo/EFO_0004827 GCST001513 Genome-wide genotyping array 2012-08-14 22566634 Benjamin DJ 2012-05-07 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22566634 The genetic architecture of economic and political preferences. Economic and political preferences (feminism/equality) 9,617 European ancestry individuals NA Illumina [628922] 12 economic and social preference http://www.ebi.ac.uk/efo/EFO_0004827 GCST001514 Genome-wide genotyping array 2012-08-14 22566634 Benjamin DJ 2012-05-07 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22566634 The genetic architecture of economic and political preferences. Economic and political preferences (immigration/crime) 9,617 European ancestry individuals NA Illumina [628922] 15 economic and social preference http://www.ebi.ac.uk/efo/EFO_0004827 GCST001515 Genome-wide genotyping array 2012-08-14 22566634 Benjamin DJ 2012-05-07 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22566634 The genetic architecture of economic and political preferences. Economic and political preferences (time) 9,617 European ancestry individuals NA Illumina [628922] 10 economic and social preference http://www.ebi.ac.uk/efo/EFO_0004827 GCST001511 Genome-wide genotyping array 2011-03-18 21298027 Festen EA 2011-01-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21298027 A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease. Crohn's disease and celiac disease 3,230 European ancestry Crohn's disease cases, 768 European ancestry celiac disease cases, 6,251 European ancestry controls 1,835 European ancestry Crohn's disease cases, 3,149 European ancestry celiac disease cases, 6,383 European ancestry controls Affymetrix, Illumina [471504] 2 celiac disease, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0001060, http://www.ebi.ac.uk/efo/EFO_0000384 GCST000955 Genome-wide genotyping array 2009-01-06 19065144 Sullivan PF 2008-12-09 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19065144 Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. Major depressive disorder 1,738 European ancestry cases, 1,802 European ancestry controls 6,079 European ancestry cases, 5,893 European ancestry controls Perlegen [435291] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST000293 Genome-wide genotyping array 2008-06-16 17447842 Libioulle C 2007-03-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/17447842 Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. Crohn's disease 547 European ancestry cases, 928 European ancestry controls 1,266 European ancestry cases, 559 European ancestry controls, Up to 428 European ancestry trios Illumina [302451] 3 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000014 Genome-wide genotyping array 2012-06-18 22570617 Wiggs JL 2012-04-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22570617 Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma. Glaucoma (primary open-angle) 3,146 European ancestry cases, 3,487 European ancestry controls NA Illumina [495132] (imputed) 4 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST001493 Genome-wide genotyping array 2008-12-09 18802019 Burkhardt R 2008-09-18 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/18802019 Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. LDL cholesterol 2,346 Micronesian ancestry individuals NA Affymetrix [~ 500000] 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST000234 Genome-wide genotyping array 2008-12-09 18976728 Bertram L 2008-10-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18976728 Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. Alzheimer's disease 941 European ancestry cases and 404 European ancestry controls from 410 families 1,767 European ancestry cases and 838 European ancestry controls from 875 families Affymetrix [484522] 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000255 Genome-wide genotyping array 2012-07-21 22566498 Turner ST 2012-05-07 Hypertension www.ncbi.nlm.nih.gov/pubmed/22566498 Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. Response to angiotensin II receptor blocker therapy 198 European ancestry hypertensive individuals, 193 African American hypertensive individuals NA Affymetrix [~ 2300000] (imputed) 20 response to candesartan http://purl.obolibrary.org/obo/GO_1901556 GCST001520 Genome-wide genotyping array 2012-07-21 22566498 Turner ST 2012-05-07 Hypertension www.ncbi.nlm.nih.gov/pubmed/22566498 Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker. Response to angiotensin II receptor blocker therapy (opposite direction w/ diuretic therapy) 394 European ancestry hypertensive individuals, 193 African American hypertensive individuals NA Affymetrix [~ 2300000] (imputed) 5 response to candesartan http://purl.obolibrary.org/obo/GO_1901556 GCST001518 Genome-wide genotyping array 2010-01-13 20018283 Heid IM 2009-12-02 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/20018283 Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. Adiponectin levels 4,659 European ancestry individuals 13,795 European ancestry individuals Affymetrix, Illumina [2585854] (imputed) 1 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST000537 Genome-wide genotyping array 2012-07-11 22584459 Sasayama D 2012-05-15 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/22584459 Possible association of CUX1 gene polymorphisms with antidepressant response in major depressive disorder. Response to antidepressants 92 Japanese ancestry cases 136 Japanese ancestry cases Illumina [291512] 1 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST001528 Genome-wide genotyping array 2011-12-10 21983787 Barrett JH 2011-10-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21983787 Genome-wide association study identifies three new melanoma susceptibility loci. Melanoma 2,804 European ancestry cases, 7,618 European ancestry controls 5,551 European ancestry cases, 7,449 European ancestry controls Illumina [594997] 10 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST001267 Genome-wide genotyping array 2012-06-27 22570627 van Koolwijk LM 2012-05-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22570627 Common genetic determinants of intraocular pressure and primary open-angle glaucoma. Intraocular pressure 11,972 European ancestry individuals 7,482 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST001506 Genome-wide genotyping array 2011-01-16 21196492 Okada Y 2010-12-31 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21196492 Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. C-reactive protein 10,112 Japanese ancestry individuals 2,742 Japanese ancestry individuals Illumina [477784] 4 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST000933 Genome-wide genotyping array 2008-08-27 19165924 Hofmann S 2008-08-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19165924 Genome-wide association study identifies ANXA11 as a new susceptibility locus for sarcoidosis. Sarcoidosis 499 European ancestry cases, 490 European ancestry controls 1,649 cases, 1,832 controls Affymetrix [375771] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST000218 Genome-wide genotyping array 2012-04-18 22425255 Lopez LM 2012-03-15 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/22425255 A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity. White matter integrity 535 European ancestry individuals NA Illumina [542050] 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST001446 Genome-wide genotyping array 2012-05-25 22493691 Eriksson N 2012-04-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/22493691 Novel associations for hypothyroidism include known autoimmune risk loci. Hypothyroidism 3,736 European ancestry cases, 35,546 European ancestry controls NA Illumina [870065] 19 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST001474 Genome-wide genotyping array 2012-08-10 22737229 Nishida N 2012-06-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/22737229 Genome-wide association study confirming association of HLA-DP with protection against chronic hepatitis B and viral clearance in Japanese and Korean. Hepatitis B (viral clearance) 181 East Asian ancestry HBV carriers, 184 East Asian ancestry controls, 185 East Asian ancestry spontaneously HBV-resolved individuals Up to 8,045 East Asian ancestry HBV carriers, up to 9,003 East Asian ancestry controls, up to 3,995 East Asian ancestry spontaneously HBV-resolved individuals Affymetrix [597789] 4 hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004197 GCST001582 Genome-wide genotyping array 2008-06-16 18198356 Hakonarson H 2008-01-15 Diabetes www.ncbi.nlm.nih.gov/pubmed/18198356 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. Type 1 diabetes 467 European ancestry trios, 561 European ancestry cases, 1,143 European ancestry controls 946 European ancestry cases and 1,098 European ancestry controls from 549 families, 364 European ancestry trios Illumina [543071] 1 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000141 Genome-wide genotyping array 2012-06-26 22560479 Forno E 2012-05-02 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/22560479 Genome-wide association study of the age of onset of childhood asthma. Asthma (childhood onset) 573 European ancestry children 107 European ancestry children, 591 Hispanic children, 233 children Illumina [512296] 5 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST001502 Genome-wide genotyping array 2015-05-06 22633400 Kosova G 2012-05-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22633400 Genome-wide association study identifies candidate genes for male fertility traits in humans. Male fertility 269 Hutterite males NA Affymetrix [248210] 6 birth rate, male fertility, family size http://www.ebi.ac.uk/efo/EFO_0004804, http://www.ebi.ac.uk/efo/EFO_0004803, http://www.ebi.ac.uk/efo/EFO_0004802 GCST001540 Genome-wide genotyping array 2012-05-25 22484627 Bradfield JP 2012-04-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22484627 A genome-wide association meta-analysis identifies new childhood obesity loci. Obesity 5,530 European ancestry cases, 8,318 European ancestry controls 2,214 European ancestry cases, 2,674 European ancestry controls Affymetrix, Illumina [2700000] (imputed) 5 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001475 Genome-wide genotyping array 2012-07-09 22561531 Wan YI 2012-05-05 Thorax www.ncbi.nlm.nih.gov/pubmed/22561531 Genome-wide association study to identify genetic determinants of severe asthma. Asthma 933 European ancestry cases, 3,346 European ancestry controls 231 European ancestry cases, 1,345 European ancestry controls Illumina [6103628] (imputed) 7 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001508 Genome-wide genotyping array 2011-09-28 21878436 Sampietro ML 2011-08-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21878436 A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention. Coronary restenosis 295 European ancestry cases, 571 European ancestry controls 455 European ancestry cases, 2,880 European ancestry controls Illumina [556099] 1 Coronary Restenosis http://www.ebi.ac.uk/efo/EFO_0004224 GCST001214 Genome-wide genotyping array 2012-06-20 22556244 Kenny EE 2012-05-04 Science www.ncbi.nlm.nih.gov/pubmed/22556244 Melanesian blond hair is caused by an amino acid change in TYRP1. Hair color 43 Solomon Islander ancestry blond haired individuals, 42 Solomon Islander ancestry dark haired individuals NA Illumina [589241] 1 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST001507 Genome-wide genotyping array 2011-01-04 21042317 Wray NR 2010-11-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21042317 Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned. Major depressive disorder 2,431 European ancestry cases, 3,673 European ancestry controls 3,332 European ancestry cases, 3,228 European ancestry controls Affymetrix, Illumina [1251157] (imputed) 4 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST000856 Genome-wide genotyping array 2011-08-05 21750109 Rafnar T 2011-07-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21750109 European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene. Bladder cancer 2,234 European ancestry cases, 41,603 European ancestry controls 3,371 European ancestry cases, 10,261 European ancestry controls, 269 Iranian ancestry cases, 246 Iranian ancestry controls Illumina [5340737] (imputed) 1 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST001153 Genome-wide genotyping array 2008-06-16 18264097 Eeles RA 2008-02-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18264097 Multiple newly identified loci associated with prostate cancer susceptibility. Prostate cancer 1,854 European ancestry cases, 1,894 European ancestry controls 3,268 European ancestry cases, 3,366 European ancestry controls Illumina [541129] 12 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000152 Genome-wide genotyping array 2013-05-21 23437003 Paternoster L 2013-02-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23437003 Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure. Bone mineral density up to 5,878 European ancestry individuals up to 1,052 European ancestry individuals Illumina [2401124] (imputed) 7 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST001870 Genome-wide genotyping array 2011-01-04 21051773 Scerri TS 2010-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21051773 PCSK6 is associated with handedness in individuals with dyslexia. Handedness in dyslexia 192 individuals 573 European ancestry individuals Illumina [~ 2000000] (imputed) 1 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST000868 Genome-wide genotyping array 2014-03-09 24024966 Teumer A 2013-08-14 J Clin Periodontol www.ncbi.nlm.nih.gov/pubmed/24024966 Genome-wide association study of chronic periodontitis in a general German population. Periodontitis (DPAL) up to 2,501 European ancestry individuals NA Affymetrix, Illumina [up to 17585496] (imputed) 15 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST002129 Genome-wide genotyping array 2014-03-09 24024966 Teumer A 2013-08-14 J Clin Periodontol www.ncbi.nlm.nih.gov/pubmed/24024966 Genome-wide association study of chronic periodontitis in a general German population. Periodontitis (PAL4Q3) up to 2,969 European ancestry individuals NA Affymetrix, Illumina [up to 17585496] (imputed) 18 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST002136 Genome-wide genotyping array 2014-03-09 24024966 Teumer A 2013-08-14 J Clin Periodontol www.ncbi.nlm.nih.gov/pubmed/24024966 Genome-wide association study of chronic periodontitis in a general German population. Periodontitis (Mean PAL) up to 4,032 European ancestry individuals NA Affymetrix, Illumina [up to 17585496] (imputed) 37 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST002127 Genome-wide genotyping array 2014-03-09 24024966 Teumer A 2013-08-14 J Clin Periodontol www.ncbi.nlm.nih.gov/pubmed/24024966 Genome-wide association study of chronic periodontitis in a general German population. Periodontitis (CDC/AAP) up to 3,915 European ancestry individuals NA Affymetrix, Illumina [up to 17585496] (imputed) 28 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST002126 Genome-wide genotyping array 2012-01-24 22197929 Yu XQ 2011-12-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22197929 A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy. IgA nephropathy 1,434 Han Chinese ancestry cases, 4,270 Han Chinese ancestry controls 2,703 Han Chinese ancestry cases, 3,464 Han Chinese ancestry controls Illumina [444882] 9 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST001364 Genome-wide genotyping array 2012-08-16 22692763 Liu CT 2012-06-12 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/22692763 Assessment of gene-by-sex interaction effect on bone mineral density. Bone mineral density (sex interaction) 16,297 European ancestry female individuals, 9,056 European ancestry male individuals 17,949 European, East Asian, and Hispanic ancestry female individuals, 6,814 European, East Asian, and Hispanic ancestry male individuals Illumina [> 2300000] (imputed) 0 sex interaction measurement, bone density http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0003923 GCST001566 Genome-wide genotyping array 2011-04-12 21399633 Gharavi AG 2011-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21399633 Genome-wide association study identifies susceptibility loci for IgA nephropathy. Nephropathy 1,194 Han Chinese ancestry cases, 902 Han Chinese ancestry controls 712 Han Chinese ancestry cases, 748 Han Chinese ancestry controls, 1,238 European ancestry cases, 1,172 European ancestry controls Illumina [498322] 5 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST001009 Genome-wide genotyping array 2011-08-03 21750679 Allanore Y 2011-07-07 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21750679 Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. Systemic sclerosis 564 European ancestry cases, 1,776 European ancestry controls 1,682 European ancestry cases, 3,926 European ancestry controls Illumina [489814] 7 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST001146 Genome-wide genotyping array 2011-05-27 21570397 Lucena MI 2011-04-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/21570397 Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles. Drug-induced liver injury (amoxicillin-clavulanate) 201 European ancestry cases, 532 European ancestry controls NA Illumina [822927] 2 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST001036 Genome-wide genotyping array 2011-12-10 21981779 Denny JC 2011-10-07 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21981779 Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies. Hypothyroidism 1,317 European ancestry cases, 5,053 European ancestry controls 263 European ancestry cases, 1,616 European ancestry controls Illumina [522164] 1 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST001265 Genome-wide genotyping array 2012-03-27 22403646 Froguel P 2012-03-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/22403646 A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels. Haptoglobin levels 631 European ancestry children 2,957 European ancestry family members, 1,434 European ancestry individuals Illumina [318237] 1 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST001435 Genome-wide genotyping array 2012-07-11 22532574 Stevens KN 2012-04-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22532574 Identification of a novel percent mammographic density locus at 12q24. Percent mammographic density 1,241 European ancestry female individuals 9,126 European ancestry individuals Illumina [2510880] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001489 Genome-wide genotyping array 2012-04-03 22399527 Kristiansson K 2012-03-07 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/22399527 Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits. Metabolic syndrome 2,637 European ancestry cases, 7,927 European ancestry controls NA Illumina [1257079] (imputed) 22 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST001436 Genome-wide genotyping array 2012-10-09 22863734 Ludwig KU 2012-08-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22863734 Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. Orofacial clefts Up to 666 European ancestry trios, 399 European ancestry cases, 1,318 European ancestry controls up to 795 East Asian ancestry trios NR [497084] 31 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST001628 Genome-wide genotyping array 2011-08-15 21779176 Winkelmann J 2011-07-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21779176 Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. Restless legs syndrome 922 European ancestry cases, 1,526 European ancestry controls 3,935 European ancestry cases, 5,754 European ancestry controls Affymetrix [301406] 6 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST001159 Genome-wide genotyping array 2011-11-16 22003152 Grallert H 2011-10-14 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/22003152 Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies. Lipoprotein-associated phospholipase A2 activity and mass 12,126 European ancestry individuals, 1,538 individuals NA Affymetrix, Illumina [2661766] (imputed) 7 lipoprotein-associated phospholipase A(2) measurement http://www.ebi.ac.uk/efo/EFO_0004746 GCST001273 Genome-wide genotyping array 2014-02-04 23853074 Meder B 2013-07-12 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/23853074 A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy. Idiopathic dilated cardiomyopathy 909 European ancestry cases, 2,120 European ancestry controls 3,234 European ancestry cases, 5,590 European ancestry controls Affymetrix [292367] 0 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST002093 Genome-wide genotyping array 2010-11-05 20921969 Aberg K 2010-10-05 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/20921969 Genome-wide association study of antipsychotic-induced QTc interval prolongation. Antipsychotic drug-induced QTc interval prolongation 738 European, African American, Hispanic, and other ancestry Schizophrenia cases NA Affymetrix [492000] 3 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST000822 Genome-wide genotyping array 2012-09-26 22821403 Ellinghaus D 2012-07-23 Hepatology www.ncbi.nlm.nih.gov/pubmed/22821403 Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4. Sclerosing cholangitis and ulcerative colitis (combined) Up to 389 European ancestry primary sclerosing cholangitis cases, 987 European ancestry ulcerative colitis cases, 2,968 European ancestry controls 1,012 European ancestry primary sclerosing cholangitis cases, 4,444 European ancestry ulcerative colitis cases, 11,659 European ancestry controls Affymetrix [up to 1279891] (imputed) 2 ulcerative colitis, sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0004268 GCST001615 Genome-wide genotyping array 2013-08-01 23505323 Weissglas-Volkov D 2013-03-15 J Med Genet www.ncbi.nlm.nih.gov/pubmed/23505323 Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. Hypertriglyceridemia 1,122 Mexican ancestry cases, 1,118 Mexican ancestry controls 1,067 Mexican ancestry cases, 1,054 Mexican ancestry controls Illumina [1361436] (imputed) 9 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST001905 Genome-wide genotyping array 2013-08-02 23505323 Weissglas-Volkov D 2013-03-15 J Med Genet www.ncbi.nlm.nih.gov/pubmed/23505323 Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. HDL cholesterol 1,122 Mexican ancestry hypertriglyceridemia cases, 1,118 Mexican ancestry controls 1,067 Mexican ancestry hypertriglyceridemia cases, 1,054 Mexican ancestry controls Illumina [1361436] (imputed) 5 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST001904 Genome-wide genotyping array 2012-07-27 22566624 Castano Betancourt MC 2012-05-07 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22566624 Genome-wide association and functional studies identify the DOT1L gene to be involved in cartilage thickness and hip osteoarthritis. Osteoarthritis 6,523 European ancestry individuals 4,442 European ancestry individuals Illumina [2455290] (imputed) 1 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST001516 Genome-wide genotyping array 2012-08-07 22683712 Freilinger T 2012-06-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22683712 Genome-wide association analysis identifies susceptibility loci for migraine without aura. Migraine 2,326 European ancestry cases, 4,580 European ancestry controls 2,508 European ancestry cases, 2,652 European ancestry controls Illumina [1246388] (imputed) 10 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST001563 Genome-wide genotyping array 2013-05-09 23381795 Verweij N 2013-02-04 Hypertension www.ncbi.nlm.nih.gov/pubmed/23381795 Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1. Circulating vasoactive peptide levels 3,444 European ancestry individuals 3,230 European ancestry individuals Illumina [2269099] (imputed) 7 vasoactive peptide measurement http://www.ebi.ac.uk/efo/EFO_0005196 GCST001853 Genome-wide genotyping array 2010-11-15 20887962 Jee SH 2010-10-08 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20887962 Adiponectin concentrations: a genome-wide association study. Adiponectin levels 4,001 Korean ancestry individuals 2,304 Korean ancestry individuals Affymetrix [up to 354357] 1 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST000828 Genome-wide genotyping array 2012-02-24 21886157 Suhre K 2011-08-31 Nature www.ncbi.nlm.nih.gov/pubmed/21886157 Human metabolic individuality in biomedical and pharmaceutical research. Metabolic traits 2,820 European ancestry individuals NA Affymetrix, Illumina [534665] 37 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST001217 Genome-wide genotyping array 2013-01-10 23065704 Amin Al Olama A 2012-10-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23065704 A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease. Prostate cancer 5,132 European ancestry non-aggressive cases, 5,953 European ancestry aggressive cases, 11,463 European ancestry controls 22,387 European ancestry non-aggressive cases, 2,008 European ancestry aggressive cases, up to 24,726 European ancestry controls Illumina [~ 2600000] (imputed) 4 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001714 Genome-wide genotyping array 2011-05-27 21546767 Murea M 2011-05-05 Am J Nephrol www.ncbi.nlm.nih.gov/pubmed/21546767 Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes. Dialysis-related mortality 610 African American type 2 diabetes cases NA Affymetrix [832357] 26 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST001066 Genome-wide genotyping array 2015-05-11 22037903 Crosslin DR 2011-10-30 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22037903 Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. White blood cell count 12,046 European ancestry individuals, 1,487 African ancestry individuals NA Illumina [532566] 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST001302 Genome-wide genotyping array 2015-05-21 21386754 Marciante KD 2011-03-06 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/21386754 Cerivastatin, genetic variants, and the risk of rhabdomyolysis. Cerivastatin-induced rhabdomyolysis 168 European ancestry cases, 636 European ancestry controls, 17 cases, 96 controls NA Illumina [292461] 1 response to statin, rhabdomyolysis http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0003867 GCST001002 Genome-wide genotyping array 2012-01-20 22188591 Anantharaman R 2011-12-21 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/22188591 Genome-wide association study identifies PERLD1 as asthma candidate gene. Asthma 490 Chinese ancestry cases, 490 Chinese ancestry controls 521 Chinese ancestry cases, 524 Chinese ancestry controls Affymetrix [683349] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001360 Genome-wide genotyping array 2012-02-07 22238593 Palmer ND 2012-01-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/22238593 A genome-wide association search for type 2 diabetes genes in African Americans. Type 2 diabetes 965 African American cases, 1,029 African American controls 2,167 African American cases, 2,288 African American controls Affymetrix [832357] 4 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001369 Genome-wide genotyping array 2012-08-07 22610502 Kennedy RB 2012-05-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Immune reponse to smallpox (secreted IL-12p40) Up to 512 European ancestry individuals, up to 199 African American individuals NA Illumina [NR] 10 response to vaccine, cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0004873 GCST001537 Genome-wide genotyping array 2012-08-07 22610502 Kennedy RB 2012-05-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Immune reponse to smallpox (secreted IL-2) Up to 512 European ancestry individuals, up to 199 African American individuals NA Illumina [NR] 17 response to vaccine, cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0004873 GCST001535 Genome-wide genotyping array 2012-08-07 22610502 Kennedy RB 2012-05-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Immune reponse to smallpox (secreted IL-10) Up to 512 European ancestry individuals, up to 199 African American individuals NA Illumina [NR] 6 response to vaccine, cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0004873 GCST001534 Genome-wide genotyping array 2012-08-07 22610502 Kennedy RB 2012-05-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Immune reponse to smallpox (secreted IL-1beta) Up to 512 European ancestry individuals, up to 199 African American individuals NA Illumina [NR] 13 response to vaccine, cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0004873 GCST001533 Genome-wide genotyping array 2012-08-07 22610502 Kennedy RB 2012-05-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Immune response to smallpox vaccine (IL-6) Up to 512 European ancestry individuals, 199 African American individuals NA Illumina [NR] 9 response to vaccine, cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0004873 GCST001532 Genome-wide genotyping array 2012-08-07 22610502 Kennedy RB 2012-05-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Immune reponse to smallpox (secreted TNF-alpha) Up to 512 European ancestry individuals, up to 199 African American individuals NA Illumina [NR] 6 response to vaccine, cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0004873 GCST001536 Genome-wide genotyping array 2012-08-07 22610502 Kennedy RB 2012-05-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22610502 Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients. Immune reponse to smallpox (secreted IFN-alpha) Up to 512 European ancestry individuals, up to 199 African American individuals NA Illumina [NR] 32 response to vaccine, cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004645, http://www.ebi.ac.uk/efo/EFO_0004873 GCST001538 Genome-wide genotyping array 2013-10-31 23668334 Shan J 2013-05-13 J Transl Med www.ncbi.nlm.nih.gov/pubmed/23668334 Genome scan study of prostate cancer in Arabs: identification of three genomic regions with multiple prostate cancer susceptibility loci in Tunisians. Prostate cancer 90 Tunisian ancestry cases, 131 Tunisian ancestry controls 155 Arab ancestry cases, 182 Arab ancestry controls Affymetrix [534781] 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002024 Genome-wide genotyping array 2014-02-04 23857890 Power RA 2013-07-15 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23857890 Genome-wide association analysis accounting for environmental factors through propensity-score matching: application to stressful live events in major depressive disorder. Major depressive disorder 805 European ancestry cases, 805 European ancestry controls NA Illumina [457670] 2 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST002095 Genome-wide genotyping array 2012-09-12 22763110 Zeggini E 2012-07-03 Lancet www.ncbi.nlm.nih.gov/pubmed/22763110 Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study. Osteoarthritis 7,410 European ancestry cases, 11,009 European ancestry controls 7,473 European ancestry cases, 42,938 European ancestry controls Illumina [485491] 4 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST001592 Genome-wide genotyping array 2013-08-21 21897333 Irvin MR 2011-12-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/21897333 Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men. Fat distribution (HIV) 192 European ancestry male cases NA Illumina [319818] 17 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST001343 Genome-wide genotyping array 2012-11-13 20125193 Cirulli ET 2010-02-03 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20125193 Common genetic variation and performance on standardized cognitive tests. Cognitive performance Up to 813 European ancestry individuals, up to 167 East Asian ancestry individuals, up to 7 Hispanic/Latin American individuals, up to 74 South Asian ancestry individuals NA Illumina [up to 563855] 62 neuropsychological test http://www.ebi.ac.uk/efo/EFO_0003926 GCST000579 Genome-wide genotyping array 2010-09-02 20639392 Eijgelsheim M 2010-07-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20639392 Genome-wide association analysis identifies multiple loci related to resting heart rate. Resting heart rate 38,991 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 10 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST000731 Genome-wide genotyping array 2013-05-30 23533358 Liu Z 2013-02-28 ScientificWorldJournal www.ncbi.nlm.nih.gov/pubmed/23533358 NCK2 is significantly associated with opiates addiction in African-origin men. Addiction 1,393 European ancestry females, 1,131 European ancestry males, 568 African ancestry females, 535 African ancestry males NA Illumina [859185] 3 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST001880 Genome-wide genotyping array 2014-03-15 24009623 Jiang J 2013-08-30 Front Genet www.ncbi.nlm.nih.gov/pubmed/24009623 Genome-wide association study for biomarker identification of Rapamycin and Everolimus using a lymphoblastoid cell line system. Response to mTOR inhibitor (everolimus) 87 European ancestry individuals, 91 African American individuals, 94 Han Chinese ancestry individuals NA Affymetrix, Illumina [1348798] 8 response to mTOR inhibitor http://www.ebi.ac.uk/efo/EFO_0005417 GCST002157 Genome-wide genotyping array 2014-03-15 24009623 Jiang J 2013-08-30 Front Genet www.ncbi.nlm.nih.gov/pubmed/24009623 Genome-wide association study for biomarker identification of Rapamycin and Everolimus using a lymphoblastoid cell line system. Response to mTOR inhibitor (rapamycin) 87 European ancestry individuals, 91 African American individuals, 94 Han Chinese ancestry individuals NA Affymetrix, Illumina [1348798] 5 response to mTOR inhibitor http://www.ebi.ac.uk/efo/EFO_0005417 GCST002156 Genome-wide genotyping array 2012-01-10 22171074 Tan A 2011-12-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22171074 A genome-wide association and gene-environment interaction study for serum triglycerides levels in a healthy Chinese male population. Triglycerides 1,999 Han Chinese ancestry male individuals 1,496 Han Chinese ancestry male individuals Illumina [1940243] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST001367 Genome-wide genotyping array 2015-06-23 23870195 Wojczynski MK 2013-07-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/23870195 Genetics of coronary artery calcification among African Americans, a meta-analysis. Coronary artery calcification 5,823 African American individuals 9,992 European ancestry individuals Affymetrix, Illumina [up to 2727966] (imputed) 48 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST002097 Genome-wide genotyping array 2010-03-25 20195514 Pillas D 2010-02-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20195514 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. Primary tooth development (number of teeth) 5,752 European ancestry related individuals NA Illumina [300766] 9 odontogenesis http://purl.obolibrary.org/obo/GO_0042476 GCST000610 Genome-wide genotyping array 2010-03-25 20195514 Pillas D 2010-02-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20195514 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. Primary tooth development (time to first tooth eruption) 5,919 European ancestry related individuals NA Illumina [300766] 6 odontogenesis http://purl.obolibrary.org/obo/GO_0042476 GCST000609 Genome-wide genotyping array 2012-01-06 22142827 Innocenti F 2011-12-05 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/22142827 A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303. Response to gemcitabine in pancreatic cancer 294 European ancestry cases NA Illumina [330690] 3 response to gemcitabine http://purl.obolibrary.org/obo/GO_0036272 GCST001346 Genome-wide genotyping array 2011-12-20 22126837 LeBlanc M 2011-11-28 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/22126837 Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function. Cognitive function 190 European ancestry schizophrenia cases, 157 European ancestry bipolar disorder cases, 353 European ancestry controls NA Affymetrix [550291] 2 mental process http://www.ebi.ac.uk/efo/EFO_0004323 GCST001332 Genome-wide genotyping array 2010-10-07 20852631 Antoniou AC 2010-09-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20852631 A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. Breast cancer 1,193 European ancestry cases, 1,190 European ancestry controls 2,974 European ancestry cases, 3,012 European ancestry controls Illumina [555616] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000801 Genome-wide genotyping array 2014-02-08 23871474 Psychosis Endophenotypes International Consortium 2013-07-17 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23871474 A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation. Psychosis 1,239 European ancestry cases, 3,596 European ancestry control 10,352 cases, 24,474 controls Affymetrix [695193] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST002096 Genome-wide genotyping array 2014-02-05 23875689 Hong SN 2013-07-22 J Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/23875689 Colorectal cancer-susceptibility single-nucleotide polymorphisms in Korean population. Colorectal cancer 105 Korean ancestry cases 189 Korean ancestry cases, 190 Korean ancestry controls Illumina [NR] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002099 Genome-wide genotyping array 2011-01-27 21221998 Kim JJ 2011-01-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21221998 A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease. Kawasaki disease 186 Korean ancestry child cases, 600 Korean ancestry controls 514 East Asian ancestry child cases, 1,042 East Asian ancestry controls Affymetrix [641760] 2 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST000939 Genome-wide genotyping array 2013-11-16 20639394 Kang TW 2010-07-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20639394 Genome-wide association of serum bilirubin levels in Korean population. Bilirubin levels 8,841 Korean ancestry individuals 1,096 Korean ancestry individuals Affymetrix [1227049] (imputed) 14 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST000730 Genome-wide genotyping array 2013-08-07 23572186 Zheng HF 2013-04-09 J Med Genet www.ncbi.nlm.nih.gov/pubmed/23572186 Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm. Bone mineral density 5,866 European ancestry individuals 715 Mexican American individuals Illumina [NR] (imputed) 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST001962 Genome-wide genotyping array 2012-03-13 22310353 Man M 2012-02-07 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/22310353 Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis. Treatment response for severe sepsis 1,446 individuals NA Illumina [856627] 8 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST001402 Genome-wide genotyping array 2013-09-24 23593202 Ran S 2013-04-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/23593202 Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche. Femoral neck bone geometry and menarche (age at onset) 1,728 European ancestry individuals 501 European ancestry individuals, 826 Chinese ancestry individuals Affymetrix [760794] 6 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST001950 Genome-wide genotyping array 2008-06-16 17522711 Lencz T 2007-03-20 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/17522711 Converging evidence for a pseudoautosomal cytokine receptor gene locus in schizophrenia. Schizophrenia 178 European ancestry cases, 144 European ancestry controls NA Affymetrix [439511] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000016 Genome-wide genotyping array 2013-11-29 23726366 Coram MA 2013-05-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23726366 Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. LDL cholesterol 7,861 African American individuals, 3,425 Hispanic individuals 7,138 African American individuals Affymetrix [NR] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST002042 Genome-wide genotyping array 2013-11-29 23726366 Coram MA 2013-05-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23726366 Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. Triglycerides 7,601 African American individuals, 3,335 Hispanic individuals 7,138 African American individuals Affymetrix [NR] 7 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST002044 Genome-wide genotyping array 2013-12-03 23726366 Coram MA 2013-05-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23726366 Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations. HDL cholesterol 7,917 African American individuals, 3,506 Hispanic individuals 7,138 African American individuals Affymetrix [NR] 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST002043 Genome-wide genotyping array 2012-07-04 22542470 Ovsyannikova IG 2012-04-25 Vaccine www.ncbi.nlm.nih.gov/pubmed/22542470 Genome-wide association study of antibody response to smallpox vaccine. Immune response to smallpox vaccine (IL-6) 217 African American individuals, 580 European ancestry individuals, 217 Hispanic individuals NA Illumina [NR] 37 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST001491 Genome-wide genotyping array 2012-02-10 21931564 Nicholson G 2011-09-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21931564 A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection. Metabolite levels 142 European ancestry female twins 202 European ancestry individuals Illumina [2541644] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST001220 Genome-wide genotyping array 2012-07-17 22658654 Chung SJ 2012-05-30 Parkinsonism Relat Disord www.ncbi.nlm.nih.gov/pubmed/22658654 Genomic determinants of motor and cognitive outcomes in Parkinson's disease. Parkinson's disease (motor and cognition) 443 European ancestry cases NA NR [198345] 5 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST001546 Genome-wide genotyping array 2011-04-13 21424380 Sehrawat B 2011-03-19 Hum Genet www.ncbi.nlm.nih.gov/pubmed/21424380 Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility. Breast cancer 302 European ancestry female cases, 321 European ancestry female controls 1,153 European ancestry female cases, 1,215 European ancestry female controls Affymetrix [782838] 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001012 Genome-wide genotyping array 2015-05-08 22295569 Karunas AS 2011-11-01 Mol Biol (Mosk) www.ncbi.nlm.nih.gov/pubmed/22295569 [Genome-wide association study of bronchial asthma in the Volga-Ural region of Russia]. Asthma 141 Russian ancestry cases, 120 Tatar ancestry cases, 69 Bashkir ancestry cases, 145 Russian ancestry controls, 111 Tatar ancestry controls, 92 Bashkir ancestry controls 202 Russian, Tatar, and Bashkir ancestry cases, 109 Russian ancestry controls, 54 Tatar ancestry controls, 53 Bashkir ancestry controls Illumina [550915] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001306 Genome-wide genotyping array 2012-07-16 22482804 Ellinghaus D 2012-04-06 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22482804 Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci. Crohn's disease and psoriasis 2,529 European ancestry psoriasis cases, 2,142 European ancestry Crohn's disease cases, 10,460 European ancestry controls Up to 3,187 European ancestry psoriasis cases, 4,073 European ancestry Crohn's disease cases, 10,100 European ancestry controls Affymetrix, Illumina, Perlegen [1116213] (imputed) 4 psoriasis, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000676, http://www.ebi.ac.uk/efo/EFO_0000384 GCST001473 Genome-wide genotyping array 2009-05-26 19442274 Fei Y 2009-05-14 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/19442274 Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study. Behcet's disease 152 cases, 170 controls NA Affymetrix [~ 500000] 0 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST000399 Genome-wide genotyping array 2010-02-10 20096396 Kung AW 2010-01-20 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20096396 Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. Bone mineral density 785 Han Chinese ancestry extreme high and low BMD female individuals 264 Han Chinese ancestry High BMD individuals, 456 Han Chinese ancestry Low BMD individuals, 3,465 Han Chinese ancestry individuals, 13,913 European ancestry individuals Illumina [488853] 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000572 Genome-wide genotyping array 2009-01-12 19047183 Friedman RA 2008-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/19047183 GRM7 variants confer susceptibility to age-related hearing impairment. Hearing impairment 846 European ancestry cases, 846 European ancestry controls 63 European ancestry cases, 67 European ancestry controls Affymetrix [506627] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST000275 Genome-wide genotyping array 2012-08-09 22566560 Malhotra AK 2012-05-07 Arch Gen Psychiatry www.ncbi.nlm.nih.gov/pubmed/22566560 Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain. Antipsychotic drug-induced weight gain 77 European ancestry individuals, 32 African American individuals, 30 individuals 183 European ancestry individuals, 22 African American individuals Illumina [803582] 1 antipsychotic drug related weight gain http://www.ebi.ac.uk/efo/EFO_0004567 GCST001517 Genome-wide genotyping array 2012-03-13 22303337 Wang K 2011-07-05 Front Genet www.ncbi.nlm.nih.gov/pubmed/22303337 Pathway-Wide Association Study Implicates Multiple Sterol Transport and Metabolism Genes in HDL Cholesterol Regulation. HDL cholesterol 653 European ancestry high HDL-C individuals, 784 European ancestry low HDL-C individuals 496 European ancestry high HDL-C individuals, 373 European ancestry low HDL-C individuals Affymetrix [681050] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST001143 Genome-wide genotyping array 2014-03-26 24025145 Chung S 2013-09-11 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/24025145 A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients. Adverse response to chemotherapy in breast cancer (alopecia) 303 Japanese ancestry cases, 880 Japanese ancestry controls 23 Japanese ancestry cases Illumina [555600] 3 chemotherapy-induced alopecia http://www.ebi.ac.uk/efo/EFO_0005400 GCST002181 Genome-wide genotyping array 2014-03-26 24025145 Chung S 2013-09-11 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/24025145 A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients. Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+epirubicin+/-5FU) 116 Japanese ancestry cases, 108 Japanese ancestry controls NA Illumina [555600] 3 response to 5-fluorouracil, response to cyclophosphamide, chemotherapy-induced alopecia, response to 4'-epidoxorubicin http://purl.obolibrary.org/obo/GO_0036275, http://purl.obolibrary.org/obo/GO_1902518, http://www.ebi.ac.uk/efo/EFO_0005400, http://purl.obolibrary.org/obo/GO_1902522 GCST002176 Genome-wide genotyping array 2014-03-27 24025145 Chung S 2013-09-11 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/24025145 A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients. Adverse response to chemotherapy in breast cancer (alopecia) (cyclophosphamide+doxorubicin+/-5FU) 64 Japanese ancestry cases, 27 Japanese ancestry controls NA Illumina [555600] 8 response to 5-fluorouracil, response to cyclophosphamide, chemotherapy-induced alopecia, response to doxorubicin http://purl.obolibrary.org/obo/GO_0036275, http://purl.obolibrary.org/obo/GO_1902518, http://www.ebi.ac.uk/efo/EFO_0005400, http://purl.obolibrary.org/obo/GO_1902520 GCST002178 Genome-wide genotyping array 2014-03-26 24025145 Chung S 2013-09-11 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/24025145 A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients. Adverse response to chemotherapy in breast cancer (alopecia) (paclitaxel) 57 Japanese ancestry cases, 63 Japanese ancestry controls NA Illumina [555600] 5 chemotherapy-induced alopecia, methylcobalamin deficiency type cblE http://www.ebi.ac.uk/efo/EFO_0005400, http://purl.obolibrary.org/obo/MONDO_0009354 GCST002179 Genome-wide genotyping array 2014-03-26 24025145 Chung S 2013-09-11 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/24025145 A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients. Adverse response to chemotherapy in breast cancer (alopecia) (docetaxel) 62 Japanese ancestry cases, 42 Japanese ancestry controls NA Illumina [555600] 4 chemotherapy-induced alopecia, response to docetaxel trihydrate http://www.ebi.ac.uk/efo/EFO_0005400, http://purl.obolibrary.org/obo/GO_1902519 GCST002180 Genome-wide genotyping array 2014-03-26 24025145 Chung S 2013-09-11 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/24025145 A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients. Adverse response to chemotherapy in breast cancer (alopecia) (anti-microtubule) 119 Japanese ancestry cases, 105 Japanese ancestry controls NA Illumina [555600] 7 chemotherapy-induced alopecia, response to antimicrotubule agent http://www.ebi.ac.uk/efo/EFO_0005400, http://www.ebi.ac.uk/efo/EFO_0005260 GCST002177 Genome-wide genotyping array 2015-04-28 22666496 Shiffman D 2012-05-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/22666496 Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy. Coronary heart disease event reduction (statin therapy interaction) 682 European, African American, Hispanic, Asian, Pacific Islander and other ancestry cases with events, 383 cases with events 29 European, African American, Hispanic, Asian, Pacific Islander and other ancestry cases with events, 2,398 European, African American, Hispanic, Asian, Pacific Islander and other ancestry cases without events, 729 cases with events, 9,563 cases without events Illumina [~ 1400000] 1 response to statin, coronary artery disease http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0001645 GCST001545 Genome-wide genotyping array 2014-04-04 24023260 Wu Y 2013-09-10 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/24023260 Genetic association with lipids in Filipinos: waist circumference modifies an APOA5 effect on triglyceride levels. Lipid traits 1,782 Filipino ancestry mothers 1,719 Filipino ancestry offsprings Affymetrix [~ 3700000] (imputed) 6 total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004612 GCST002174 Genome-wide genotyping array 2012-03-20 22387998 Tanikawa C 2012-03-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22387998 A genome-wide association study identifies two susceptibility loci for duodenal ulcer in the Japanese population. Duodenal ulcer 1,043 Japanese ancestry cases, 21,694 Japanese ancestry controls 5,992 Japanese ancestry cases, 3,629 Japanese ancestry controls Illumina [480327] 2 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST001433 Genome-wide genotyping array 2012-07-17 22634755 Dunlop MG 2012-05-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22634755 Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. Colorectal cancer 8,323 European ancestry cases, 9,457 European ancestry controls 19,513 European ancestry cases, 17,657 European ancestry controls, 1,583 Japanese ancestry cases, 1,898 Japanese ancestry controls Illumina [NR] (imputed) 3 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST001544 Genome-wide genotyping array 2012-03-27 22384361 Cheng YC 2011-01-11 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/22384361 Genome-wide association analysis of ischemic stroke in young adults. Stroke 466 European ancestry cases, 377 African American cases, 46 East Asian, Asian, and other ancestry cases, 523 European ancestry controls, 357 African American controls, 47 East Asian, Asian, and other ancestry controls 1,586 European ancestry cases, 2,690 European ancestry controls Illumina [1421999] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST000940 Genome-wide genotyping array 2009-09-28 17846124 Hayes MG 2007-09-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/17846124 Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies. Type 2 diabetes 281 Mexican American cases, 280 Mexican American controls 1,087 European ancestry individuals, 440 Pima Indian ancestry cases, 455 Pima Indian ancestry controls, 124 Amish cases, 295 Amish controls Affymetrix [88142] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000075 Genome-wide genotyping array 2010-09-02 20639878 Singer JB 2010-07-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20639878 A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury. Lumiracoxib-related liver injury 31 European ancestry cases, 3 Hispanic cases, 1 case, 176 European, Hispanic and other ancestry controls 79 European ancestry cases, 16 Hispanic ancestry cases, 1 case, 405 European, Hispanic and other ancestry controls Affymetrix [682386] 1 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST000735 Genome-wide genotyping array 2012-06-22 22605921 Gibson J 2012-04-28 Mol Vis www.ncbi.nlm.nih.gov/pubmed/22605921 Genome-wide association study of primary open angle glaucoma risk and quantitative traits. Glaucoma (primary open-angle) 387 European ancestry cases, 5,380 European ancestry controls 294 European ancestry cases, 50 European ancestry controls Affymetrix [681552] 0 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST001498 Genome-wide genotyping array 2012-07-10 22569225 Krintel SB 2012-05-06 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/22569225 Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis. Response to TNF-alpha inhibitors in rheumatoid arthritis 196 European ancestry cases NA Illumina [486450] 8 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST001510 Genome-wide genotyping array 2013-12-11 23760081 Kim YJ 2013-06-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23760081 A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. Chronic hepatitis B infection 400 Korean ancestry cases, 1,000 Korean ancestry controls 971 Korean ancestry cases, 1,938 Korean ancestry controls Illumina [719265] 6 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST002068 Genome-wide genotyping array 2010-09-01 20622881 Gretarsdottir S 2010-07-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20622881 Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. Abdominal aortic aneurysm 1,292 European ancestry cases, 30,503 European ancestry controls 3,267 European ancestry cases, 7,451 European ancestry controls Illumina [293677] 2 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST000727 Genome-wide genotyping array 2010-05-23 20400778 Morrison AC 2010-04-17 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20400778 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. Mortality in heart failure 1,645 European ancestry cases, 881 European ancestry controls, 281 African ancestry cases, 185 African ancestry controls NA Affymetrix [up to 2366858] (imputed) 11 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST000661 Genome-wide genotyping array 2009-02-25 19125160 Feulner TM 2009-01-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19125160 Examination of the current top candidate genes for AD in a genome-wide association study. Alzheimer's disease 491 European ancestry cases, 479 European ancestry controls NA Illumina [~ 550000] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000313 Genome-wide genotyping array 2009-01-21 19132087 Burgner D 2009-01-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19132087 A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease. Kawasaki disease 107 European ancestry cases, 134 European ancestry controls 583 European ancestry cases, 1,357 European ancestry controls from 583 families Affymetrix [223922] 2 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST000314 Genome-wide genotyping array 2014-03-28 24023788 Ong BA 2013-09-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/24023788 Gene network analysis in a pediatric cohort identifies novel lung function genes. Lung function (FEV1) 1,015 European ancestry individuals, 541 African American individuals NA Illumina [up to 524000] 9 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST002165 Genome-wide genotyping array 2014-03-28 24023788 Ong BA 2013-09-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/24023788 Gene network analysis in a pediatric cohort identifies novel lung function genes. Lung function (FEV1/FVC) 1,015 European ancestry individuals, 541 African American individuals NA Illumina [up to 524000] 5 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST002164 Genome-wide genotyping array 2014-03-28 24023788 Ong BA 2013-09-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/24023788 Gene network analysis in a pediatric cohort identifies novel lung function genes. Lung function (FVC) 1,015 European ancestry individuals, 541 African American individuals NA Illumina [up to 524000] 9 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST002162 Genome-wide genotyping array 2014-03-28 24023788 Ong BA 2013-09-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/24023788 Gene network analysis in a pediatric cohort identifies novel lung function genes. Lung function (forced expiratory flow during mid-portion (25% and 75%) of forced vital capacity) 1,015 European ancestry individuals, 541 African American individuals NA Illumina [up to 524000] 12 maximal midexpiratory flow rate http://www.ebi.ac.uk/efo/EFO_0004313 GCST002163 Genome-wide genotyping array 2012-03-19 22344219 Wen W 2012-02-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22344219 Meta-analysis identifies common variants associated with body mass index in east Asians. Body mass index 22,762 East Asian ancestry individuals, 2,522 Malay ancestry individuals, 2,431 Chinese, Malay and Asian Indian ancestry individuals 53,215 East Asian ancestry results, 2,118 Malay ancestry individuals Affymetrix, Illumina [2474474] (imputed) 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001415 Genome-wide genotyping array 2013-06-26 23508266 Duan QL 2013-03-19 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/23508266 A genome-wide association study of bronchodilator response in asthmatics. Asthma (bronchodilator response) Up to 403 European ancestry asthmatic children and their parents 764 European ancestry cases, 592 Costa Rican ancestry cases Illumina [534290] 2 response to bronchodilator http://purl.obolibrary.org/obo/GO_0097366 GCST001911 Genome-wide genotyping array 2013-09-16 23633212 Rinella ES 2013-04-30 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/23633212 Genome-wide association of single-nucleotide polymorphisms with weight loss outcomes after Roux-en-Y gastric bypass surgery. Weight loss (gastric bypass surgery) 86 European ancestry individuals with least EBWL, 89 European ancestry individuals with most EBWL 164 European ancestry individuals with least EBWL, 169 European ancestry individuals with most EBWL Affymetrix [730767] 2 body weight loss http://www.ebi.ac.uk/efo/EFO_0005245 GCST001985 Genome-wide genotyping array 2011-06-08 21623375 Albagha OM 2011-05-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21623375 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. Paget's disease 741 European ancestry cases, 2,699 European ancestry controls 1,474 European ancestry cases, 1,671 European ancestry controls Illumina [2487078] (imputed) 9 osteitis deformans http://www.ebi.ac.uk/efo/EFO_0004261 GCST001086 Genome-wide genotyping array 2010-07-12 20585626 Long J 2010-06-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20585626 Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium. Breast cancer 2,073 Chinese ancestry cases, 2,084 Chinese ancestry controls 15,159 East Asian ancestry cases, 12,993 East Asian ancestry controls, 2,797 European ancestry cases, 2,662 European ancestry controls Affymetrix [684457] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000709 Genome-wide genotyping array 2010-08-17 20610895 Koriyama H 2010-07-02 J Atheroscler Thromb www.ncbi.nlm.nih.gov/pubmed/20610895 Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. Peripheral artery disease 195 Japanese ancestry cases, 1,358 Japanese ancestry controls 699 Japanese ancestry cases, 1,540 Japanese ancestry controls Perlegen [222285] 2 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST000720 Genome-wide genotyping array 2011-07-30 21743469 Evans DM 2011-07-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21743469 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Ankylosing spondylitis 3,023 European ancestry cases, 8,779 European ancestry controls 2,111 European ancestry cases, 4,483 European ancestry controls Illumina [2223620] (imputed) 13 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST001149 Genome-wide genotyping array 2012-03-27 22359512 Demirkan A 2012-02-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22359512 Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. Phospholipid levels (plasma) 4,034 European ancestry individuals NA Illumina [NR] (imputed) 25 phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004639 GCST001414 Genome-wide genotyping array 2012-03-27 22359512 Demirkan A 2012-02-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22359512 Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations. Sphingolipid levels 4,034 European ancestry individuals NA Illumina [NR] (imputed) 10 sphingolipid measurement http://www.ebi.ac.uk/efo/EFO_0004622 GCST001413 Genome-wide genotyping array 2011-07-30 21703177 Thompson AJ 2011-05-20 J Hepatol www.ncbi.nlm.nih.gov/pubmed/21703177 Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients. IFN-related cytopenia 984 European ancestry with genotype 1 HCV cases, 201 African American genotype 1 HCV cases, 99 Hispanic genotype 1 HCV cases NA Illumina [565759] 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST001076 Genome-wide genotyping array 2012-07-13 22628157 Levine AJ 2012-05-24 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/22628157 Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults. HIV-associated dementia 1,287 European ancestry HIV-infected male individuals NA Illumina [~ 2500000] (imputed) 4 AIDS dementia http://www.ebi.ac.uk/efo/EFO_0002608 GCST001542 Genome-wide genotyping array 2014-04-02 24023777 Miyake A 2013-09-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/24023777 Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3. Adolescent idiopathic scoliosis (severe) 554 Japanese ancestry cases, 1,474 Japanese ancestry controls 839 East Asian ancestry cases, 10,149 East Asian ancestry controls Illumina [455121] 1 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST002169 Genome-wide genotyping array 2013-09-16 23535732 Eeles RA 2013-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23535732 Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array. Prostate cancer 11,085 European ancestry cases, 11,463 European ancestry controls 19,662 European ancestry cases, 19,715 European ancestry controls Illumina [~ 2600000] (imputed) 23 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001942 Genome-wide genotyping array 2012-04-03 22412388 Kenny EE 2012-03-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22412388 A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci. Crohn's disease 737 Ashkenazi Jewish cases, 2,257 Ashkenazi Jewish controls 971 Ashkenazi Jewish cases, 2,124 Ashkenazi Jewish controls Affymetrix, Illumina [1060934] (imputed) 17 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST001438 Genome-wide genotyping array 2010-03-09 20154673 Van Deerlin VM 2010-02-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20154673 Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions. Frontotemporal lobar degeneration 515 European ancestry cases, 2,509 European ancestry controls 89 European ancestry cases, 553 European ancestry controls Illumina [~ 500000] 0 Pick disease http://www.ebi.ac.uk/efo/EFO_0003096 GCST000595 Genome-wide genotyping array 2012-05-18 22438815 Lill CM 2012-03-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22438815 Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database. Parkinson's disease 2,197 cases, 2,061 controls Up to 98,080 European and Asian ancestry individuals Illumina, Perlegen [7123920] (imputed) 6 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST001445 Genome-wide genotyping array 2011-09-08 21810271 Antoni G 2011-08-02 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/21810271 Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. vWF and FVIII levels 1,624 European ancestry individuals NA Illumina [442728] 11 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST001188 Genome-wide genotyping array 2015-04-22 23754948 Randall JC 2013-06-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23754948 Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits. Sexual dimorphism in anthropometric traits up to 60,586 European ancestry males, up to 73,137 European ancestry females up to 62,395 European ancestry males, up to 74,657 European ancestry females Affymetrix, Illumina [2846694] (imputed) 10 sexual dimorphism http://www.ebi.ac.uk/efo/EFO_0005951 GCST002063 Genome-wide genotyping array 2011-11-15 22003120 Burdon KP 2011-10-14 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/22003120 Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconus. Corneal structure 319 European ancestry cases, 3,462 European ancestry controls 615 European ancestry cases, 702 European ancestry controls Illumina [745982] 0 keratoconus http://purl.obolibrary.org/obo/MONDO_0015486 GCST001274 Genome-wide genotyping array 2011-11-24 22019779 Takahashi Y 2011-10-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22019779 A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis. Scoliosis 1,033 Japanese ancestry adolescent female cases, 1,473 Japanese ancestry female controls 326 Japanese ancestry adolescent female cases, 9,823 Japanese ancestry female controls Illumina [455121] 1 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST001293 Genome-wide genotyping array 2011-09-30 21900290 Qi Q 2011-09-06 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/21900290 Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes. Lp (a) levels 1,450 European ancestry individuals NA Illumina [~ 2500000] (imputed) 4 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST001218 Genome-wide genotyping array 2011-08-20 21811574 van Manen D 2011-07-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/21811574 Genome-wide association scan in HIV-1-infected individuals identifying variants influencing disease course. HIV-1 progression 404 cases NA Illumina [309494] 0 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST001171 Genome-wide genotyping array 2011-05-02 21460842 Cha PC 2011-04-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21460842 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. Uterine fibroids 1,607 Japanese ancestry cases, 1,428 Japanese ancestry controls 3,439 Japanese ancestry cases, 3,244 Japanese ancestry controls Illumina [457044] 5 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST001027 Genome-wide genotyping array 2010-07-01 20532800 Bostrom MA 2010-06-08 Hum Genet www.ncbi.nlm.nih.gov/pubmed/20532800 Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA. End-stage renal disease (non-diabetic) 464 African American cases, 478 African American controls 336 African American cases, 363 African American controls Illumina [~ 550000] 1 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST000696 Genome-wide genotyping array 2014-03-26 24001895 Kelly TN 2013-09-03 Hypertension www.ncbi.nlm.nih.gov/pubmed/24001895 Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci. Blood pressure 22,275 East Asian ancestry individuals, 4,325 South East Asian ancestry individuals 28,783 East Asian ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 6 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST002167 Genome-wide genotyping array 2011-09-06 21810746 Chantarangsu S 2011-08-01 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/21810746 Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash. Nevirapine-induced rash 72 Thai ancestry nevirapine-induced rash HIV cases, 77 Thai ancestry nevirapine-tolerant rash HIV cases 88 Thai ancestry nevirapine-induced rash HIV cases, 145 Thai ancestry nevirapine-tolerant HIV cases Illumina [499730] 3 response to reverse transcriptase inhibitor http://purl.obolibrary.org/obo/GO_0061479 GCST001186 Genome-wide genotyping array 2012-02-10 22267201 Stolk L 2012-01-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22267201 Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways. Menopause (age at onset) 38,968 European ancestry female individuals Up to 14,435 European ancestry female individuals Affymetrix, Illumina [2551160] (imputed) 19 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST001381 Genome-wide genotyping array 2010-08-12 20596022 Petukhova L 2010-07-01 Nature www.ncbi.nlm.nih.gov/pubmed/20596022 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. Alopecia areata Up to 1,054 European ancestry cases, 3,278 European ancestry controls NA Illumina [463301] 8 alopecia areata http://www.ebi.ac.uk/efo/EFO_0004192 GCST000719 Genome-wide genotyping array 2011-11-18 22004471 Frank J 2011-10-18 Addict Biol www.ncbi.nlm.nih.gov/pubmed/22004471 Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster. Alcohol dependence 1,333 European ancestry male cases, 2,168 European ancestry male controls NA Illumina [463044] 6 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001281 Genome-wide genotyping array 2011-03-02 21283782 Tore S 2011-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21283782 Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis. Nephrolithiasis 80 Sardinian cases, 94 Sardinian controls 125 European ancestry cases, 157 European ancestry controls Affymetrix [334674] 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST000951 Genome-wide genotyping array 2012-03-30 22399142 Jongjaroenprasert W 2012-03-08 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22399142 A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis. Thyrotoxic hypokalemic periodic paralysis 78 Thai ancestry cases, 74 Thai ancestry controls 28 Thai ancestry cases, 48 Thai ancestry controls Illumina [508393] 1 thyrotoxic periodic paralysis http://purl.obolibrary.org/obo/MONDO_0019201 GCST001437 Genome-wide genotyping array 2010-07-14 20598377 Nischwitz S 2010-06-30 J Neuroimmunol www.ncbi.nlm.nih.gov/pubmed/20598377 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. Multiple sclerosis 590 European ancestry cases, 825 European ancestry controls NA Illumina [~ 300000] 4 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000716 Genome-wide genotyping array 2011-11-08 21998595 N'Diaye A 2011-10-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21998595 Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry. Height 20,427 African ancestry individuals Up to 16,436 African American individuals Affymetrix, Illumina [3310998] (imputed) 33 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST001263 Genome-wide genotyping array 2010-08-11 20610541 Lascorz J 2010-07-07 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/20610541 Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. Colorectal cancer 371 European ancestry cases, 1,263 European ancestry controls 4,915 European ancestry cases, 8,159 European ancestry controls Affymetrix [610664] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000722 Genome-wide genotyping array 2010-06-13 20453841 Kochi Y 2010-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20453841 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. Rheumatoid arthritis 2,303 Japanese ancestry cases, 3,380 Japanese ancestry controls 4,768 Japanese ancestry cases, 17,359 Japanese ancestry controls Illumina [393217] 4 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000677 Genome-wide genotyping array 2010-05-10 20205591 Pelak K 2010-04-15 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/20205591 Host determinants of HIV-1 control in African Americans. HIV-1 viral setpoint 515 African American cases NA Illumina [1212217] 10 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST000656 Genome-wide genotyping array 2010-04-27 20370913 Ma L 2010-04-06 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/20370913 Genome-wide association analysis of total cholesterol and high-density lipoprotein cholesterol levels using the Framingham heart study data. Cholesterol 6,078 individuals 1,231 European ancestry individuals NR [432096] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST000647 Genome-wide genotyping array 2010-04-14 20339536 Barber MJ 2010-03-22 PLoS One www.ncbi.nlm.nih.gov/pubmed/20339536 Genome-wide association of lipid-lowering response to statins in combined study populations. Response to statin therapy 3,928 European ancestry individuals NA Illumina [~ 2500000] (imputed) 36 response to statin http://purl.obolibrary.org/obo/GO_0036273 GCST000635 Genome-wide genotyping array 2011-09-21 21841780 Chu X 2011-08-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21841780 A genome-wide association study identifies two new risk loci for Graves' disease. Graves' disease 1,468 Chinese ancestry cases, 1,490 Chinese ancestry controls 3,994 Chinese ancestry cases, 3,510 Chinese ancestry controls Illumina [486049] 11 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST001200 Genome-wide genotyping array 2010-06-08 20453840 Sanna S 2010-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20453840 Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. Multiple sclerosis 882 Sardinian cases, 872 Sardinian controls 1,775 Sardinian cases, 2,005 Sardinian controls Affymetrix [6607266] (imputed) 2 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000680 Genome-wide genotyping array 2011-11-04 22004137 Liu L 2011-10-01 Viral Immunol www.ncbi.nlm.nih.gov/pubmed/22004137 A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease progression of chronic HBV infection. Hepatitis B 1,944 Han Chinese ancestry progressed cases, 854 Han Chinese ancestry asymptomatic carriers NA Affymetrix [NR] 1 hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004197 GCST001257 Genome-wide genotyping array 2010-03-29 20235792 Uhl GR 2010-03-01 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/20235792 Genome-wide association for smoking cessation success: participants in the Patch in Practice trial of nicotine replacement. Smoking cessation 108 Abstinent individuals , 216 Non-abstinent individuals NA Affymetrix [NR] 0 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST000616 Genome-wide genotyping array 2011-08-27 21804548 Hirota T 2011-07-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21804548 Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population. Asthma 1,532 Japanese ancestry cases, 3,304 Japanese ancestry controls 5,639 Japanese ancestry cases, 24,608 Japanese ancestry controls Illumina [458847] 14 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001183 Genome-wide genotyping array 2011-08-12 21784300 Mick E 2011-07-13 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/21784300 Genome-wide association study of the child behavior checklist dysregulation profile. Attention deficit hyperactivity disorder 341 ADHD case offspring from 339 trios NA Illumina [835136] 7 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST001154 Genome-wide genotyping array 2011-08-05 21750111 Mbarek H 2011-07-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21750111 A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population. Hepatitis B 458 Japanese ancestry cases, 2,056 Japanese ancestry controls 2,209 Japanese ancestry cases, 4,440 Japanese ancestry controls Illumina [423627] 4 hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004197 GCST001150 Genome-wide genotyping array 2012-03-17 22383897 Long J 2012-02-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22383897 Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer. Breast cancer 2,918 Chinese ancestry cases, 2,324 Chinese ancestry controls up to 16,173 East Asian ancestry cases, up to 18,282 East Asian ancestry controls Affymetrix [690947] 3 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001420 Genome-wide genotyping array 2012-03-09 22306650 Thye T 2012-02-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22306650 Common variants at 11p13 are associated with susceptibility to tuberculosis. Tuberculosis 1,329 African ancestry cases, 1,847 African ancestry controls 2,024 African ancestry cases, 5,154 African ancestry controls, 1,025 Indonesian ancestry cases, 983 Indonesian ancestry controls, 4,441 European ancestry cases, 5,874 European ancestry controls Affymetrix [793964] 1 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST001398 Genome-wide genotyping array 2015-05-14 22174851 Lingappa JR 2011-12-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/22174851 Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure. HIV-1 viral setpoint 496 African ancestry cases NA Illumina [990115] 14 HIV viral set point measurement http://www.ebi.ac.uk/efo/EFO_0006319 GCST001352 Genome-wide genotyping array 2015-05-14 22174851 Lingappa JR 2011-12-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/22174851 Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure. HIV-1 susceptibility 496 African ancestry cases and 302 African ancestry exposed controls from serodiscordant couples NA Illumina [990115] 9 HIV-1 infection, Susceptibility to viral and mycobacterial infections http://www.ebi.ac.uk/efo/EFO_0000180, http://www.orpha.net/ORDO/Orphanet_391311 GCST001353 Genome-wide genotyping array 2011-07-30 21743057 Schumacher FR 2011-07-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21743057 Genome-wide association study identifies new prostate cancer susceptibility loci. Prostate cancer 2,782 European ancestry cases, 4,458 European ancestry controls 7,358 European ancestry cases, 6,732 European ancestry controls Illumina [571243] 14 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001147 Genome-wide genotyping array 2012-01-27 22170493 Ellinghaus E 2011-12-15 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/22170493 Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL. Psoriatic arthritis 535 European ancestry cases, 3,432 European ancestry controls 1,931 European ancestry cases, 6,785 European ancestry controls Illumina [1160703] (imputed) 2 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST001355 Genome-wide genotyping array 2010-09-22 20709820 Kong X 2010-08-13 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/20709820 Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema. Emphysema-related traits 2,383 European ancestry cases NA Illumina [499578] 7 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST000770 Genome-wide genotyping array 2011-06-29 21665990 Yu Y 2011-06-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21665990 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. Age-related macular degeneration 2,594 European ancestry cases, 4,134 European ancestry controls 5,640 European ancestry cases, 52,174 European ancestry controls Affymetrix [6036699] (imputed) 11 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST001100 Genome-wide genotyping array 2011-09-17 21844665 Hu HJ 2011-08-16 Exp Mol Med www.ncbi.nlm.nih.gov/pubmed/21844665 Common variants at the promoter region of the APOM confer a risk of rheumatoid arthritis. Rheumatoid arthritis 100 Korean ancestry cases, 600 Korean ancestry controls 578 Korean ancestry cases, 711 Korean ancestry controls Affymetrix [300909] 1 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST001203 Genome-wide genotyping array 2011-06-01 21531791 Sanson M 2011-04-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21531791 Chromosome 7p11.2 (EGFR) variation influences glioma risk. Glioma 4,147 European ancestry cases, 7,435 European ancestry controls NA Illumina [424460] 7 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST001058 Genome-wide genotyping array 2011-08-12 21768215 Tin A 2011-07-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21768215 Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele. Urate levels 8,651 African American individuals 1,996 African American individuals Affymetrix [NR] (imputed) 5 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST001163 Genome-wide genotyping array 2011-11-08 21989058 Qin Y 2011-10-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21989058 Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF). Premature ovarian failure 391 Han Chinese ancestry cases, 895 Han Chinese ancestry controls 400 Han Chinese ancestry cases, 800 Han Chinese ancestry controls Affymetrix [642069] 1 primary ovarian insufficiency http://www.ebi.ac.uk/efo/EFO_0004266 GCST001284 Genome-wide genotyping array 2013-08-02 23502783 Weinhold N 2013-03-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23502783 The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Multiple myeloma (hyperdiploidy) up to 1,660 European ancestry cases, 7,306 European ancestry controls Illumina [414804] 14 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST001907 Genome-wide genotyping array 2013-08-02 23502783 Weinhold N 2013-03-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23502783 The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma. Multiple myeloma (IgH translocation) up to 1,660 European ancestry cases, 7,306 European ancestry controls Illumina [414804] (imputed) 25 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST001906 Genome-wide genotyping array 2011-11-30 22012869 Hinney A 2011-10-19 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/22012869 Genome-wide association study in German patients with attention deficit/hyperactivity disorder. Attention deficit hyperactivity disorder 495 European ancestry child and adolescent cases, 1,300 European ancestry adult controls 1,023 European ancestry individuals from 320 families, 2455 European ancestry cases and 896 European ancestry controls from 2,064 trios Illumina [487484] 2 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST001287 Genome-wide genotyping array 2013-05-08 23894747 Aberg KA 2013-02-01 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/23894747 A comprehensive family-based replication study of schizophrenia genes. Schizophrenia 11,185 European ancestry cases, 10,768 European ancestry controls 1,262 African American ancestry individuals, 2,740 European ancestry individuals, 2,296 Asian ancestry individuals NR [1085772] (imputed) 14 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001851 Genome-wide genotyping array 2011-10-07 21926416 Amos CI 2011-09-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21926416 Genome-wide association study identifies novel loci predisposing to cutaneous melanoma. Melanoma 1,804 European ancestry cases, 1,026 European ancestry controls 6,483 European and Middle East/North African ancestry cases, 23,324 European and Middle East/North African ancestry controls Illumina [818977] 1 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST001245 Genome-wide genotyping array 2012-04-25 22449649 Loo SK 2012-02-28 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/22449649 Genome-wide association study of intelligence: additive effects of novel brain expressed genes. Intelligence 656 European ancestry individuals from ADHD families NA Illumina [795637] 21 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST001428 Genome-wide genotyping array 2013-11-03 23669352 Graff M 2013-05-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23669352 Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course. Body mass index Up to 13,627 European ancestry individuals Up to 16,253 European ancestry individuals Affymetrix, Illumina [557887] (imputed) 14 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002021 Genome-wide genotyping array 2012-01-27 22216198 Athanasiadis G 2011-12-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/22216198 A genome-wide association study of the Protein C anticoagulant pathway. Anticoagulant levels 397 European ancestry individuals from 21 families NA Illumina [283437] 8 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST001365 Genome-wide genotyping array 2009-01-07 19030899 Lei SF 2008-11-23 Hum Genet www.ncbi.nlm.nih.gov/pubmed/19030899 Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci. Height 618 Chinese ancestry individuals 2,953 Chinese ancestry individuals Affymetrix [281533] 1 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000272 Genome-wide genotyping array 2013-12-11 23752247 Loukola A 2013-06-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23752247 Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample. Smoking behavior 1,114 European ancestry twins 5,294 European ancestry twins Illumina [2614137] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST002070 Genome-wide genotyping array 2012-02-09 22267200 Gudmundsson J 2012-01-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22267200 Discovery of common variants associated with low TSH levels and thyroid cancer risk. Thyroid cancer 27,758 European ancestry individuals 1,156 European ancestry cases, up to 42,617 European ancestry controls Illumina [~ 16000000] (imputed) 3 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST001382 Genome-wide genotyping array 2013-11-15 23704207 Wu X 2013-05-23 Cancer Res www.ncbi.nlm.nih.gov/pubmed/23704207 Genome-wide association study of genetic predictors of overall survival for non-small cell lung cancer in never smokers. Non-small cell lung cancer (survival) 620 European ancestry never smoker cases 1,256 Chinese ancestry never smoker cases Illumina [NR] 0 survival time, non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0003060 GCST002032 Genome-wide genotyping array 2013-08-28 23818313 Kim HJ 2012-11-06 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/23818313 Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians. Obesity 756 Mongolian ancestry individuals from 55 families 1,301 Korean ancestry individuals Illumina [567072] 3 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001732 Genome-wide genotyping array 2014-02-04 23874384 Viding E 2013-07-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/23874384 Genetics of callous-unemotional behavior in children. Callous-unemotional behaviour 2,930 European ancestry children NA Affymetrix [1724317] (imputed) 3 callous-unemotional behaviour http://www.ebi.ac.uk/efo/EFO_0005322 GCST002092 Genome-wide genotyping array 2012-10-24 20881960 Lango Allen H 2010-09-29 Nature www.ncbi.nlm.nih.gov/pubmed/20881960 Hundreds of variants clustered in genomic loci and biological pathways affect human height. Height 133,653 European ancestry individuals 50,074 European ancestry individuals Affymetrix, Illumina [2834208] (imputed) 199 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST000817 Genome-wide genotyping array 2014-03-04 23934736 Yu B 2013-08-11 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/23934736 Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study. Metabolite levels (Dihydroxy docosatrienoic acid) 1,260 African American individuals NA Affymetrix [~ 2500000] (imputed) 20 dihydroxy docosatrienoic acid measurement http://www.ebi.ac.uk/efo/EFO_0005275 GCST002120 Genome-wide genotyping array 2014-03-04 23934736 Yu B 2013-08-11 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/23934736 Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study. Metabolite levels (Pyroglutamine) 1,260 African American individuals NA Affymetrix [~ 2500000] (imputed) 23 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST002118 Genome-wide genotyping array 2014-03-04 23934736 Yu B 2013-08-11 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/23934736 Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study. Metabolite levels (X-11787) 1,260 African American individuals NA Affymetrix [~ 2500000] (imputed) 29 hydroxy-leucine measurement http://www.ebi.ac.uk/efo/EFO_0005276 GCST002119 Genome-wide genotyping array 2013-05-02 23358160 Borglum AD 2013-01-29 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23358160 Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. Schizophrenia (cytomegalovirus infection interaction) 888 European ancestry cases, 882 European ancestry controls 2539 European ancestry cases, 5486 European ancestry controls Illumina [541148] 1 schizophrenia, cytomegalovirus infection http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0001062 GCST001833 Genome-wide genotyping array 2013-05-02 23358160 Borglum AD 2013-01-29 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23358160 Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. Schizophrenia 888 European ancestry cases, 882 European ancestry controls 2539 European ancestry cases, 5486 European ancestry controls Illumina [541148] 3 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001839 Genome-wide genotyping array 2011-05-24 21460841 Naj AC 2011-04-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21460841 Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease. Alzheimer's disease (late onset) 8,309 European ancestry cases, 7,366 European ancestry controls 10,523 European ancestry cases, 28,231 European ancestry controls Affymetrix, Illumina [2324889] (imputed) 9 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001026 Genome-wide genotyping array 2013-04-23 23350875 Fernandez-Rozadilla C 2013-01-26 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/23350875 A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12. Colorectal cancer 882 European ancestry cases, 473 European ancestry controls 1,436 European ancestry cases, 1,780 European ancestry controls Affymetrix [674718] 3 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST001832 Genome-wide genotyping array 2011-06-01 21521612 Kohli MA 2011-04-28 Neuron www.ncbi.nlm.nih.gov/pubmed/21521612 The neuronal transporter gene SLC6A15 confers risk to major depression. Major depressive disorder 353 European ancestry cases, 366 European ancestry controls 991 African Americans, 4,308 European ancestry cases, 9,661 European ancestry controls Illumina [365676] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST001056 Genome-wide genotyping array 2011-05-25 21502573 Smith NL 2011-04-21 Circulation www.ncbi.nlm.nih.gov/pubmed/21502573 Genetic predictors of fibrin D-dimer levels in healthy adults. D-dimer levels 21,052 European ancestry individuals NA Affymetrix, Illumina [2522393] (imputed) 15 D dimer measurement http://www.ebi.ac.uk/efo/EFO_0004507 GCST001049 Genome-wide genotyping array 2008-07-01 18521185 Chen WM 2008-06-04 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/18521185 Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. Fasting plasma glucose 5,088 European ancestry individuals 18,436 European ancestry individuals Illumina [315635] 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000202 Genome-wide genotyping array 2012-07-13 22526605 Howson JM 2012-04-12 Diabetologia www.ncbi.nlm.nih.gov/pubmed/22526605 Genetic association of zinc transporter 8 (ZnT8) autoantibodies in type 1 diabetes cases. Type 1 diabetes autoantibodies Up to 2,142 European ancestry cases 855 European ancestry affected family members Affymetrix, Illumina [775249] 0 type 1 diabetes mellitus, autoantibody measurement http://purl.obolibrary.org/obo/MONDO_0005147, http://www.ebi.ac.uk/efo/EFO_0004866 GCST001479 Genome-wide genotyping array 2012-01-20 21298047 Chen X 2011-01-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/21298047 The nuclear transcription factor PKNOX2 is a candidate gene for substance dependence in European-origin women. Substance dependence 2,524 European ancestry individuals, 1,103 African ancestry individuals NA Illumina [830696] 1 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST000956 Genome-wide genotyping array 2012-06-18 22613542 Chen XD 2012-03-01 Chin Med J (Engl) www.ncbi.nlm.nih.gov/pubmed/22613542 ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior. Drinking behavior 904 European ancestry individuals 1,972 European ancestry individuals from 593 families, 761 European ancestry individuals, 2,955 Han Chinese ancestry individuals Affymetrix [379319] 0 drinking behavior http://www.ebi.ac.uk/efo/EFO_0004315 GCST001429 Genome-wide genotyping array 2011-01-03 21044948 Spencer CC 2010-11-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21044948 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Parkinson's disease 1,705 European ancestry cases, 5,175 European ancestry controls 1,039 European ancestry cases, 1,984 European ancestry controls Illumina [532616] 3 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST000855 Genome-wide genotyping array 2011-09-30 21907864 Ferreira MA 2011-09-10 Lancet www.ncbi.nlm.nih.gov/pubmed/21907864 Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. Asthma 12,475 European ancestry cases, 19,967 European ancestry controls 3,322 European ancestry cases, 22,036 European ancestry controls Illumina [NR] (imputed) 4 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001226 Genome-wide genotyping array 2008-06-22 18439548 Ridker PM 2008-04-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/18439548 Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study. C-reactive protein 6,345 European ancestry female individuals NA Illumina [336108] 7 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST000178 Genome-wide genotyping array 2008-07-22 18317468 Sklar P 2008-03-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/18317468 Whole-genome association study of bipolar disorder. Bipolar disorder 1,461 European ancestry cases, 2,008 European ancestry controls 409 European ancestry trios from 256 families, 365 European ancestry cases, 351 European ancestry controls Affymetrix [372193] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000158 Genome-wide genotyping array 2008-06-22 18521091 Volpi S 2008-06-03 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/18521091 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. Response to iloperidone treatment (QT prolongation) 91 African American Schizophrenia cases, 69 European ancestry Schizophrenia cases, 16 Asian ancestry Schizophrenia cases, 7 Schizophrenia cases NA Affymetrix [339272] 6 response to iloperidone http://purl.obolibrary.org/obo/GO_0036287 GCST000201 Genome-wide genotyping array 2014-07-01 20385819 Chen W 2010-04-12 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/20385819 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. Age-related macular degeneration 2,157 European ancestry cases, 1,150 European ancestry controls 7,892 European ancestry cases, 5,998 European ancestry controls, 678 Japanese ancestry cases, 336 Japanese ancestry controls Illumina [~ 2500000] (imputed) 8 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST000652 Genome-wide genotyping array 2013-11-14 23726511 Xie P 2013-05-28 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23726511 Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. Post-traumatic stress disorder 300 European ancestry cases, up to 1,538 European ancestry controls, 444 African American cases, up to 2,936 African American controls 207 European ancestry cases, up to 1,692 European ancestry controls, 89 African American cases, up to 655 African American controls Illumina [up to 871502] 2 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST002038 Genome-wide genotyping array 2013-11-14 23726511 Xie P 2013-05-28 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23726511 Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. Post-traumatic stress disorder (asjusted for relatedness) up to 308 European ancestry cases, up to 1,538 European ancestry controls, up to 456 African American cases, up to 2,936 African American controls NA Illumina [up to 871502] 19 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST002037 Genome-wide genotyping array 2013-04-17 23297363 Cordell HJ 2013-01-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23297363 Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. Tetralogy of Fallot 835 European ancestry cases, 5,159 European ancestry controls 798 European ancestry cases, 2,931 European ancestry controls Illumina [516131] 6 Tetralogy of Fallot http://purl.obolibrary.org/obo/HP_0001636 GCST001807 Genome-wide genotyping array 2008-06-22 18521090 Lavedan C 2008-06-03 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/18521090 Association of the NPAS3 gene and five other loci with response to the antipsychotic iloperidone identified in a whole genome association study. Response to iloperidone treatment (PANSS-T score) 106 Asian, African American, European, or other ancestry individuals 104 Asian, African American, European, or other ancestry individuals Affymetrix [334563] 0 response to iloperidone http://purl.obolibrary.org/obo/GO_0036287 GCST000200 Genome-wide genotyping array 2013-08-07 23568457 Wade TD 2013-04-09 Int J Eat Disord www.ncbi.nlm.nih.gov/pubmed/23568457 Genetic variants associated with disordered eating. Anorexia nervosa 237 European ancestry female cases, 2,287 European ancestry female controls NA Illumina [6150213] (imputed) 15 eating disorder http://www.ebi.ac.uk/efo/EFO_0005203 GCST001961 Genome-wide genotyping array 2013-08-07 23568457 Wade TD 2013-04-09 Int J Eat Disord www.ncbi.nlm.nih.gov/pubmed/23568457 Genetic variants associated with disordered eating. Bulimia nervosa 151 European ancestry female cases, 2,291 European ancestry female controls NA Illumina [6150213] (imputed) 23 bulimia nervosa http://www.ebi.ac.uk/efo/EFO_0005204 GCST001958 Genome-wide genotyping array 2013-08-07 23568457 Wade TD 2013-04-09 Int J Eat Disord www.ncbi.nlm.nih.gov/pubmed/23568457 Genetic variants associated with disordered eating. Eating disorders (purging via substances) 600 European ancestry female cases, 1,921 European ancestry female controls NA Illumina [6150213] (imputed) 11 eating disorder http://www.ebi.ac.uk/efo/EFO_0005203 GCST001959 Genome-wide genotyping array 2013-08-07 23568457 Wade TD 2013-04-09 Int J Eat Disord www.ncbi.nlm.nih.gov/pubmed/23568457 Genetic variants associated with disordered eating. Eating disorders 543 European ancestry female cases, 1,116 European ancestry female controls NA Illumina [6150213] (imputed) 8 eating disorder http://www.ebi.ac.uk/efo/EFO_0005203 GCST001960 Genome-wide genotyping array 2012-08-08 22745674 Hager J 2012-06-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/22745674 Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis. Coronary heart disease 1,949 Middle Eastern ancestry individuals 2,547 Middle Eastern ancestry individuals Illumina [513079] 3 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001581 Genome-wide genotyping array 2011-11-02 21983785 Macgregor S 2011-10-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21983785 Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3. Melanoma 2,168 European ancestry cases, 4,387 European ancestry controls 5,193 European ancestry cases, 15,144 European ancestry controls Illumina [5480804] (imputed) 2 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST001266 Genome-wide genotyping array 2012-10-13 22863731 Cheung CL 2012-08-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22863731 Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3. Thyrotoxic hypokalemic periodic paralysis 69 Chinese ancestry cases, 1,170 East Asian ancestry controls 54 Chinese ancestry cases, 400 Taiwanese ancestry controls Illumina [486782] 1 thyrotoxic periodic paralysis http://purl.obolibrary.org/obo/MONDO_0019201 GCST001627 Genome-wide genotyping array 2014-01-31 23824729 van Meurs JB 2013-07-03 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/23824729 Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease. Homocysteine levels 44,147 European ancestry individuals NA Affymetrix, Illumina [2090256] (imputed) 18 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST002087 Genome-wide genotyping array 2012-10-12 22903471 Hibar DP 2012-08-18 Brain Imaging Behav www.ncbi.nlm.nih.gov/pubmed/22903471 Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects. Lentiform nucleus volume 162 European ancestry Alzheimer's disease cases, 346 European ancestry mild cognitive impairment cases, 198 European ancestry controls, 639 European ancestry individuals from 364 families NA Illumina [2380200] (imputed) 14 lentiform nucleus measurement http://www.ebi.ac.uk/efo/EFO_0004913 GCST001640 Genome-wide genotyping array 2012-04-03 22379998 McCormack M 2012-03-01 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/22379998 Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions. Adverse response to lamotrigine and phenytoin 34 European ancestry lamotrigine-induced hypersensitivity cases, 42 European ancestry phenytoin-induced hypersensitivity cases, 1,296 European ancestry controls NA Illumina [NR] 12 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST001431 Genome-wide genotyping array 2011-10-22 21956439 Zuo L 2011-09-28 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/21956439 Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q. Alcohol dependence 1,409 European ancestry cases, 1,518 European ancestry controls, 681 African American cases, 508 African American controls NA Illumina [805814] 3 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001254 Genome-wide genotyping array 2012-07-10 22589742 Fox CS 2012-05-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22589742 Genome-wide association of pericardial fat identifies a unique locus for ectopic fat. Pericardial fat 5,487 European ancestry individuals 1,442 African American individuals, 1,399 Hispanic individuals, 761 Chinese ancestry individuals Affymetrix [~ 2500000] (imputed) 1 pericardial adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0007890 GCST001522 Genome-wide genotyping array 2011-10-21 21909115 Ehret GB 2011-09-11 Nature www.ncbi.nlm.nih.gov/pubmed/21909115 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Systolic blood pressure 69,395 European ancestry individuals Up to 133,361 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 20 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST001227 Genome-wide genotyping array 2011-10-21 21909115 Ehret GB 2011-09-11 Nature www.ncbi.nlm.nih.gov/pubmed/21909115 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Hypertension 69,395 European ancestry individuals Up to 133,361 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 11 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST001238 Genome-wide genotyping array 2011-10-21 21909115 Ehret GB 2011-09-11 Nature www.ncbi.nlm.nih.gov/pubmed/21909115 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Diastolic blood pressure 69,395 European ancestry individuals Up to 133,361 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 19 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST001228 Genome-wide genotyping array 2012-09-26 22837378 Wilk JB 2012-07-26 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/22837378 Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction. Airflow obstruction up to 3,368 European ancestry cases, up to 29,507 European ancestry controls 331 European ancestry cases, 2,550 European ancestry controls Affymetrix, Illumina [up to 2500000] (imputed) 30 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST001621 Genome-wide genotyping array 2012-01-27 22086417 Cozen W 2011-11-15 Blood www.ncbi.nlm.nih.gov/pubmed/22086417 A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32. Nodular sclerosis Hodgkin lymphoma 393 European ancestry cases, 3,315 European ancestry controls 113 European ancestry cases, 214 European ancestry controls Illumina [705591] 2 nodular sclerosis Hodgkin lymphoma http://www.ebi.ac.uk/efo/EFO_0004708 GCST001323 Genome-wide genotyping array 2013-05-10 23322567 Lopes MC 2013-01-15 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/23322567 Identification of a candidate gene for astigmatism. Corneal astigmatism 22,100 European ancestry individuals Affymetrix, Illumina [2800000] (imputed) 17 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST001819 Genome-wide genotyping array 2012-03-20 22384028 Guo Y 2012-02-24 PLoS One www.ncbi.nlm.nih.gov/pubmed/22384028 A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits. Hypertension 315 Hong Kong Chinese ancestry individuals from 111 families NA Illumina [503984] 3 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST001423 Genome-wide genotyping array 2012-03-20 22388998 Zhang CK 2012-01-19 Am J Hematol www.ncbi.nlm.nih.gov/pubmed/22388998 Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation. Gaucher disease severity 139 Ashkenazi Jewish cases NA Illumina [540902] 3 Gaucher disease http://purl.obolibrary.org/obo/MONDO_0018150 GCST001380 Genome-wide genotyping array 2015-05-21 22704111 Hotaling JM 2012-06-13 J Urol www.ncbi.nlm.nih.gov/pubmed/22704111 Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort. Erectile dysfunction in type 1 diabetes 125 European ancestry cases, 403 European ancestry controls NA Illumina [840354] 6 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST001572 Genome-wide genotyping array 2011-09-28 21874001 Kooner JS 2011-08-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21874001 Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Type 2 diabetes 5,561 South Asian ancestry cases, 14,458 South Asian ancestry controls 13,170 South Asian ancestry cases, 25,398 South Asian ancestry controls Illumina [568976] 6 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001213 Genome-wide genotyping array 2011-09-30 21908515 Cai Q 2011-09-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21908515 Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium. Breast cancer 2,062 East Asian ancestry cases, 2,066 East Asian ancestry controls 15,091 East Asian ancestry cases, 14,877 East Asian ancestry controls Affymetrix [684457] 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001224 Genome-wide genotyping array 2011-12-13 22032556 Brockschmidt FF 2011-10-27 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/22032556 Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness. Male-pattern baldness 581 European ancestry male cases, 617 European ancestry male controls 461 European ancestry male cases, 151 European ancestry male controls Illumina [560387] 2 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST001297 Genome-wide genotyping array 2011-09-27 21901158 Irvin MR 2011-08-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/21901158 Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study. Insulin resistance/response 1,040 African American individuals NA Affymetrix [872243] 14 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST001208 Genome-wide genotyping array 2012-03-15 22383894 Pierce BL 2012-02-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22383894 Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh. Arsenic metabolism 1,313 Bangladeshi ancestry individuals NA Illumina [259597] 2 urinary arsenic measurement http://www.ebi.ac.uk/efo/EFO_0004880 GCST001421 Genome-wide genotyping array 2012-07-19 22664479 Han JY 2012-06-05 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/22664479 A genome-wide association study for irinotecan-related severe toxicities in patients with advanced non-small-cell lung cancer. Response to irinotecan in non-small-cell lung cancer 101 non-small-cell lung cancer cases 146 non-small-cell lung cancer cases Affymetrix [312230] 2 response to irinotecan http://www.ebi.ac.uk/efo/EFO_0004829 GCST001558 Genome-wide genotyping array 2012-08-07 22693455 Perry JR 2012-05-31 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22693455 Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. Type 2 diabetes 2,112 lean type 2 diabetes cases, 4,123 obese type 2 diabetes cases, 54,412 controls 2,881 lean type 2 diabetes cases, 8,702 obese type 2 diabetes cases, 18,957 controls NR [NR] 12 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001550 Genome-wide genotyping array 2011-11-04 21990027 Drago A 2011-10-11 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21990027 The genetics of antipsychotic induced tremors: a genome-wide pathway analysis on the STEP-BD SCP sample. Response to antipsychotic therapy (extrapyramidal side effects) 409 European and other ancestry bipolar cases NA Affymetrix [NR] 1 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST001271 Genome-wide genotyping array 2014-04-10 24114350 Zhang M 2013-10-11 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24114350 A genome-wide association study of severe teenage acne in European Americans. Acne (severe teenage) 81 European ancestry cases, 847 European ancestry controls 134 European ancestry cases, 1,258 European ancestry controls Illumina [2165857] (imputed) 0 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST002229 Genome-wide genotyping array 2015-05-05 22139419 Gieger C 2011-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/22139419 New gene functions in megakaryopoiesis and platelet formation. Mean platelet volume 13,106 European ancestry individuals, 1,652 Val Borbera (founder/genetic isolate) individuals, 593 Carlantino (founder/genetic isolate) individuals, 1,146 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,213 South Tyrolean (founder/genetic isolate) individuals, 890 Sorbian (founder/genetic isolate) individuals Up to 16,960 European ancestry individuals, 855 Cliento (founder/genetic isolate) individuals, 1,023 Talana (founder/genetic isolate) individuals Affymetrix, Illumina [~ 2500000] (imputed) 29 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST001335 Genome-wide genotyping array 2015-05-05 22139419 Gieger C 2011-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/22139419 New gene functions in megakaryopoiesis and platelet formation. Platelet count 38,891 European ancestry individuals, 1,661 Val Borbera (founder/genetic isolate) individuals, 521 Carlantino (founder/genetic isolate) individuals, 1,198 Friuli Venezia Giulia (founder/genetic isolate) individuals, 1,213 South Tyrolean (founder/genetic isolate) individuals, 890 Sorbian (founder/genetic isolate) individuals, 4,292 Sardinian (founder/genetic isolate) individuals Up to 16,949 European ancestry individuals, 854 Cliento (founder/genetic isolate) individuals, 1,035 Talana (founder/genetic isolate) individuals Affymetrix, Illumina [~ 2500000] (imputed) 56 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST001337 Genome-wide genotyping array 2011-10-16 21957438 Meschia JF 2011-09-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/21957438 Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. Stroke 1,470 European ancestry cases, 1,932 European ancestry controls NA Illumina [5156597] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST001243 Genome-wide genotyping array 2014-03-27 24124411 Park TJ 2013-09-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/24124411 Genome-wide association study of liver enzymes in korean children. Liver enzyme levels (alanine transaminase) 484 Korean ancestry children NA Illumina [747076] 11 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST002207 Genome-wide genotyping array 2014-03-27 24124411 Park TJ 2013-09-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/24124411 Genome-wide association study of liver enzymes in korean children. Liver enzyme levels (aspartate transaminase) 484 Korean ancestry children NA Illumina [747076] 8 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST002208 Genome-wide genotyping array 2013-12-06 23761726 Yazar S 2013-06-06 Mol Vis www.ncbi.nlm.nih.gov/pubmed/23761726 Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study. Corneal astigmatism 2,784 European ancestry individuals Illumina [~ 2500000] (imputed) 7 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST002064 Genome-wide genotyping array 2011-09-28 21900944 Shen H 2011-09-08 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21900944 Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels. Aspartate aminotransferase levels 866 Old Order Amish individuals NA Affymetrix [373825] 1 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST001222 Genome-wide genotyping array 2014-05-13 24204828 Zheng JS 2013-10-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/24204828 Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits. Homeostasis model assessment of beta-cell function (dietary factor interaction) 820 European ancestry individuals NA Affymetrix [590000] 12 diet measurement, HOMA-B http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004469 GCST002251 Genome-wide genotyping array 2014-05-13 24204828 Zheng JS 2013-10-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/24204828 Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits. Fasting insulin (dietary factor interaction) 820 European ancestry individuals NA Affymetrix [590000] 14 diet measurement, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004466 GCST002248 Genome-wide genotyping array 2014-05-13 24204828 Zheng JS 2013-10-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/24204828 Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits. Homeostasis model assessment of insulin resistance (dietary factor interaction) 820 European ancestry individuals NA Affymetrix [590000] 15 diet measurement, HOMA-IR http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004501 GCST002253 Genome-wide genotyping array 2008-06-16 17053108 Dewan A 2006-10-19 Science www.ncbi.nlm.nih.gov/pubmed/17053108 HTRA1 promoter polymorphism in wet age-related macular degeneration. Age-related macular degeneration (wet) 96 South East Asian ancestry cases, 130 South East Asian ancestry controls NA Affymetrix [97824] 1 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST000006 Genome-wide genotyping array 2012-06-19 22446962 Onouchi Y 2012-03-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22446962 A genome-wide association study identifies three new risk loci for Kawasaki disease. Kawasaki disease 428 Japanese ancestry cases, 3,379 Japanese ancestry controls 754 Japanese ancestry cases, 947 Japanese ancestry controls Illumina [463793] 5 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST001455 Genome-wide genotyping array 2011-09-21 21876681 Hamza TH 2011-08-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21876681 Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. Parkinson's disease (coffee consumption interaction) 1,458 European ancestry cases, 931 European ancestry controls 1,014 European ancestry cases, 1,917 European ancestry controls Illumina [811597] 0 coffee consumption, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0004330, http://purl.obolibrary.org/obo/MONDO_0005180 GCST001205 Genome-wide genotyping array 2013-07-05 23535967 Tin A 2013-03-28 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23535967 Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate. Glomerular filtration rate 9,049 European ancestry individuals Affymetrix [> 2500000] (imputed) 6 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST001923 Genome-wide genotyping array 2013-07-12 23535730 Pharoah PD 2013-04-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23535730 GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer. Ovarian cancer 3,769 European ancestry cases, 4,396 European ancestry controls 211 East Asian ancestry cases, 972 East Asian ancestry controls, 39,674 European ancestry individuals, 106 Malaysian ancestry cases, 106 Malaysian ancestry controls Illumina [2508744] (imputed) 17 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST001941 Genome-wide genotyping array 2013-11-09 20018918 Solovieff N 2009-12-16 Blood www.ncbi.nlm.nih.gov/pubmed/20018918 Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster. Fetal hemoglobin levels 848 Black cases 305 Black cases, 406 Chinese ancestry cases, 113 Thai ancestry cases Illumina [~ 600000] 3 fetal hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004576 GCST000545 Genome-wide genotyping array 2011-04-08 21378987 Holm H 2011-03-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21378987 A rare variant in MYH6 is associated with high risk of sick sinus syndrome. Sick sinus syndrome 792 European ancestry cases, 37,592 European ancestry controls 469 European ancestry cases, 1,185 European ancestry controls Illumina [~ 7200000] (imputed) 0 familial sick sinus syndrome http://purl.obolibrary.org/obo/MONDO_0012061 GCST001001 Genome-wide genotyping array 2013-06-18 23456092 Park BL 2013-03-01 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23456092 Extended genetic effects of ADH cluster genes on the risk of alcohol dependence: from GWAS to replication. Alcohol dependence 117 Korean ancestry cases, 279 Korean ancestry controls 504 Korean ancestry cases, 471 Korean ancestry controls Illumina [427349] 1 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001883 Genome-wide genotyping array 2011-10-01 21775533 Tan XL 2011-07-20 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/21775533 Genetic variation predicting cisplatin cytotoxicity associated with overall survival in lung cancer patients receiving platinum-based chemotherapy. Response to platinum-based chemotherapy in small cell and non-small cell lung cancers 91 African American lymphoblastoid cell lines, 96 European ancestry lymphoblastoid cell lines, 96 Han Chinese ancestry lymphoblastoid cell lines 222 European ancestry small cell lung cancer cases, 961 European ancestry non-small cell lung cancer cases Affymetrix, Illumina [1348798] 0 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST001169 Genome-wide genotyping array 2013-09-10 23620142 Reiner AP 2013-04-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23620142 Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Circulating myeloperoxidase levels (serum) 9,305 European ancestry individuals Affymetrix, Illumina [2397181] 5 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST001979 Genome-wide genotyping array 2013-09-10 23620142 Reiner AP 2013-04-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23620142 Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Circulating myeloperoxidase levels (plasma) 9,260 European ancestry individuals Affymetrix, Illumina [2421770] 3 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST001980 Genome-wide genotyping array 2011-10-16 21940522 Shaffer JR 2011-09-21 J Dent Res www.ncbi.nlm.nih.gov/pubmed/21940522 Genome-wide association scan for childhood caries implicates novel genes. Dental caries 1,305 European ancestry children 1,695 European ancestry children Illumina [1450678] (imputed) 3 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST001244 Genome-wide genotyping array 2008-06-16 18084291 van Es MA 2007-12-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18084291 Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 737 European ancestry cases, 721 European ancestry controls 1,030 European ancestry cases, 1,195 European ancestry controls Illumina [311946] 3 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000127 Genome-wide genotyping array 2009-09-28 17099884 Liu QR 2006-12-05 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/17099884 Addiction molecular genetics: 639,401 SNP whole genome association identifies many "cell adhesion" genes. Addiction 560 African American cases, 360 African American controls, 420 European ancestry cases, 680 European ancestry controls NA Affymetrix [639401] 0 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST000009 Genome-wide genotyping array 2015-05-12 21729881 Major JM 2011-07-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21729881 Genome-wide association study identifies common variants associated with circulating vitamin E levels. Vitamin E levels 2,402 European ancestry cases, 1612 European ancestry controls 475 European ancestry cases, 517 European ancestry controls, 1,416 cases, 1,359 controls Illumina [NR] 3 vitamin E measurement http://www.ebi.ac.uk/efo/EFO_0004867 GCST001142 Genome-wide genotyping array 2014-01-07 23805179 Hass J 2013-06-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/23805179 A Genome-Wide Association Study Suggests Novel Loci Associated with a Schizophrenia-Related Brain-Based Phenotype. Hippocampal volume in schizophrenia 170 European ancestry individuals, 158 individuals 2,020 European ancestry cases, 7,438 European ancestry controls Illumina [743591] 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST002076 Genome-wide genotyping array 2010-11-17 20935630 Speliotes EK 2010-10-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20935630 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Body mass index Up to 123,865 European ancestry individuals Up to 125,931 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2800000] (imputed) 38 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000830 Genome-wide genotyping array 2014-03-18 23974872 Ripke S 2013-08-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23974872 Genome-wide association analysis identifies 13 new risk loci for schizophrenia. Schizophrenia 5,001 European ancestry cases, 6,243 European ancestry controls, 8,832 cases, 12,067 controls 4,801 European ancestry cases, 4,741 European ancestry controls, 2,612 European and unknown ancestry cases, 15,021 European and unknown ancestry controls, 581 trios Affymetrix, Illumina [9871789] 27 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST002149 Genome-wide genotyping array 2011-07-19 21738491 Arking DE 2011-06-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21738491 Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals. Sudden cardiac arrest 1,283 European ancestry cases, ~20,000 European ancestry controls 3,119 European ancestry cases, 11,146 European ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 1 sudden cardiac arrest http://www.ebi.ac.uk/efo/EFO_0004278 GCST001132 Genome-wide genotyping array 2009-09-28 17903299 Kathiresan S 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903299 A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study. Lipid traits 1,087 European ancestry individuals ~8,100 European ancestry individuals Affymetrix [70897] 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST000078 Genome-wide genotyping array 2013-09-27 23527680 Ebejer JL 2013-04-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/23527680 Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. Attention deficit hyperactivity disorder (combined symptoms) 1,851 individuals 155 individuals Illumina [2373249] (imputed) 21 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST001931 Genome-wide genotyping array 2013-10-01 23527680 Ebejer JL 2013-04-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/23527680 Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. Attention deficit hyperactivity disorder (hyperactivity-impulsivity symptoms) 1,851 individuals 155 individuals Illumina [2373249] (imputed) 25 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST001944 Genome-wide genotyping array 2013-09-27 23527680 Ebejer JL 2013-04-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/23527680 Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. Attention deficit hyperactivity disorder (inattention symptoms) 1,851 individuals 155 individuals Illumina [2373249] (imputed) 22 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST001943 Genome-wide genotyping array 2011-05-24 21499250 Spurdle AB 2011-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21499250 Genome-wide association study identifies a common variant associated with risk of endometrial cancer. Endometrial cancer 1,265 European ancestry cases, 5,190 European ancestry controls 3,957 European ancestry cases, 6,886 European ancestry controls Illumina [519655] 2 endometrial neoplasm http://www.ebi.ac.uk/efo/EFO_0004230 GCST001040 Genome-wide genotyping array 2011-10-06 21935397 Paternoster L 2011-09-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/21935397 Genome-wide population-based association study of extremely overweight young adults--the GOYA study. Obesity (extreme) 2,633 European ancestry extremely obese adult cases, 2,740 European ancestry controls 29,181 European ancestry individuals Illumina [545349] 4 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001240 Genome-wide genotyping array 2011-07-14 21701565 Malhotra A 2011-06-23 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/21701565 A genome-wide association study of BMI in American Indians. Body mass index 1,120 Pima Indian ancestry individuals 2,133 Pima Indian ancestry individuals Affymetrix [454194] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001123 Genome-wide genotyping array 2011-09-17 21824976 Garcia-Closas M 2011-08-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21824976 A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3. Bladder cancer 4,501 European ancestry cases, 6,076 European ancestry controls 1,382 European ancestry cases, 2,201 European ancestry controls Illumina [555912] 1 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST001193 Genome-wide genotyping array 2011-12-15 22037555 Shi Y 2011-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22037555 Common variants on 8p12 and 1q24.2 confer risk of schizophrenia. Schizophrenia 3,750 Han Chinese ancestry cases, 6,468 Han Chinese ancestry controls 4,383 Han Chinese ancestry cases, 4,539 Han Chinese ancestry controls Affymetrix [546561] 2 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001301 Genome-wide genotyping array 2013-03-26 23319801 Rafiq S 2013-01-14 Cancer Res www.ncbi.nlm.nih.gov/pubmed/23319801 Identification of inherited genetic variations influencing prognosis in early-onset breast cancer. Breast cancer (prognosis) 536 European ancestry early-onset cases 1,516 European ancestry early-onset cases Illumina [487496] 5 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001816 Genome-wide genotyping array 2014-03-26 24124408 Hong KW 2013-09-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/24124408 Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations. Orthostatic hypotension 667 Korean ancestry cases, 5,761 Korean ancestry controls NA Affymetrix [333651] 5 orthostatic hypotension http://www.ebi.ac.uk/efo/EFO_0005252 GCST002209 Genome-wide genotyping array 2009-10-14 19802338 Chasman DI 2008-10-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/19802338 Genetic loci associated with plasma concentration of low-density lipoprotein cholesterol, high-density lipoprotein cholesterol, triglycerides, apolipoprotein A1, and Apolipoprotein B among 6382 white women in genome-wide analysis with replication. Lipid traits 6,382 European ancestry females 970 European ancestry individuals Illumina [314518] 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST000241 Genome-wide genotyping array 2011-09-30 21900946 Nakabayashi K 2011-09-08 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21900946 Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. Graves' disease 1,119 Japanese ancestry cases, 2,718 Japanese ancestry controls 432 Japanese ancestry cases, 1,157 Japanese ancestry controls Perlegen [268068] 7 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST001219 Genome-wide genotyping array 2011-09-21 21827660 Yang TH 2011-08-09 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/21827660 Combinations of newly confirmed Glioma-Associated loci link regions on chromosomes 1 and 9 to increased disease risk. Glioma 781 European ancestry cases, 3,992 European ancestry controls NA Illumina [489781] 1 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST001194 Genome-wide genotyping array 2011-09-02 21814517 Noguchi E 2011-07-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21814517 Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations. Asthma 938 Japanese ancestry cases, 2,376 Japanese ancestry controls 1653 East Asian ancestry cases, 1453 East Asian ancestry controls Illumina [450326] 2 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001172 Genome-wide genotyping array 2011-09-16 21826085 Tanaka S 2011-08-09 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/21826085 DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia. Tardive dyskinesia 61 Japanese ancestry schizophrenic cases, 61 Japanese ancestry cases schizophrenic controls 36 Japanese ancestry schizophrenic cases, 138 Japanese ancestry schizophrenic controls Illumina [257704] 1 movement disorder http://www.ebi.ac.uk/efo/EFO_0004280 GCST001196 Genome-wide genotyping array 2013-04-24 21705454 Huang RS 2011-06-24 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/21705454 Platinum sensitivity-related germline polymorphism discovered via a cell-based approach and analysis of its association with outcome in ovarian cancer patients. Response to platinum-based agents 87 European ancestry lymphoblastoid cell lines 52 European ancestry lymphoblastoid cell lines NR [2286186] 0 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST001127 Genome-wide genotyping array 2011-09-01 21829377 Lemaitre RN 2011-07-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829377 Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. Plasma omega-3 polyunsaturated fatty acid levels (alphalinolenic acid) 8,866 European ancestry individuals NA Affymetrix, Illumina [NR] 10 alpha-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007759 GCST001180 Genome-wide genotyping array 2011-09-01 21829377 Lemaitre RN 2011-07-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829377 Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. Plasma omega-3 polyunsaturated fatty acid level (eicosapentaenoic acid) 8,866 European ancestry individuals NA Affymetrix, Illumina [NR] 17 eicosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007760 GCST001178 Genome-wide genotyping array 2011-09-01 21829377 Lemaitre RN 2011-07-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829377 Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. Plasma omega-3 polyunsaturated fatty acid levels (docosahexaenoic acid) 8,866 European ancestry individuals NA Affymetrix, Illumina [NR] 3 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST001177 Genome-wide genotyping array 2011-09-01 21829377 Lemaitre RN 2011-07-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21829377 Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. Plasma omega-3 polyunsaturated fatty acid levels (docosapentaenoic acid) 8,866 European ancestry individuals NA Affymetrix, Illumina [NR] 20 docosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0006809 GCST001179 Genome-wide genotyping array 2010-02-08 20081856 McMahon FJ 2010-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20081856 Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. Major mood disorders 6,686 European ancestry cases, 9,068 European ancestry controls 1,930 European ancestry cases, 2,747 European ancestry controls Affymetrix, Illumina, Perlegen [~ 2100000] (imputed) 1 mood disorder http://www.ebi.ac.uk/efo/EFO_0004247 GCST000570 Genome-wide genotyping array 2012-04-28 22452962 Kim HC 2012-03-27 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/22452962 A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study. Breast cancer 2,273 Korean ancestry cases, 2,052 Korean ancestry controls 4,049 Korean ancestry cases, 3,845 Korean ancestry controls Affymetrix [555525] 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001457 Genome-wide genotyping array 2011-07-13 21701570 Ng MC 2011-06-23 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/21701570 Genome-wide association of BMI in African Americans. Body mass index 1,715 African American individuals 3,274 African American individuals Affymetrix [746626] 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001125 Genome-wide genotyping array 2011-08-15 21779381 Schurks M 2011-07-14 PLoS One www.ncbi.nlm.nih.gov/pubmed/21779381 Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study. Cardiovascular disease risk factors 5,122 European ancestry female migrain cases NA Illumina [339596] 5 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST001157 Genome-wide genotyping array 2011-10-26 21980299 Bradfield JP 2011-09-29 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21980299 A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci. Type 1 diabetes 9,934 European ancestry cases, 16,956 European ancestry controls 1,120 European ancestry affected trios Affymetrix, Illumina [~ 2540000] (imputed) 9 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST001255 Genome-wide genotyping array 2011-08-06 21764829 Png E 2011-07-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21764829 A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region. Hepatitis B vaccine response 1,683 Indonesian ancestry individuals 1,931 Indonesian ancestry individuals Illumina [455508] 3 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST001162 Genome-wide genotyping array 2011-05-13 21505071 Li Z 2011-04-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21505071 A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population. Myopia (pathological) 102 Han Chinese ancestry cases, 335 Han Chinese ancestry controls 2,891 Han Chinese ancestry cases, 10,071 Han Chinese ancestry controls Affymetrix [681783] 2 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST001044 Genome-wide genotyping array 2013-05-16 23386860 Pasquale LR 2013-01-30 Front Genet www.ncbi.nlm.nih.gov/pubmed/23386860 Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes. Type 2 diabetes (dietary heme iron intake interaction) 1,806 European ancestry cases, 2,965 European ancestry controls NA Affymetrix [681770] 4 dietary heme iron intake measurement, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0008355, http://purl.obolibrary.org/obo/MONDO_0005148 GCST001843 Genome-wide genotyping array 2011-06-20 21646302 Bielinski SJ 2011-06-06 Mayo Clin Proc www.ncbi.nlm.nih.gov/pubmed/21646302 Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. Bilirubin levels 6,307 European ancestry individuals NA Illumina [583129] 5 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST001091 Genome-wide genotyping array 2011-09-28 21878437 Mondul AM 2011-08-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21878437 Genome-wide association study of circulating retinol levels. Retinol levels 5,006 European ancestry individuals 1,124 European ancestry individuals, 3,764 individuals Illumina [562105] 2 vitamin A measurement http://www.ebi.ac.uk/efo/EFO_0004857 GCST001216 Genome-wide genotyping array 2013-09-16 23643386 Hatoum IJ 2013-05-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23643386 Weight loss after gastric bypass is associated with a variant at 15q26.1. Weight loss (gastric bypass surgery) 693 European ancestry individuals 327 European ancestry individuals Illumina [1943170] (imputed) 5 body weight loss http://www.ebi.ac.uk/efo/EFO_0005245 GCST001991 Genome-wide genotyping array 2012-02-10 22239941 Png E 2012-01-13 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/22239941 A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians. Tuberculosis 108 Indonesian ancestry cases, 115 Indonesian ancestry controls 600 Indonesian ancestry cases, 540 Indonesian ancestry controls, 1,837 European ancestry cases, 1,779 European ancestry controls Affymetrix [95207] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST001377 Genome-wide genotyping array 2011-09-15 21826682 Isackson PJ 2011-08-08 Muscle Nerve www.ncbi.nlm.nih.gov/pubmed/21826682 Association of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: evidence for additional functions of EYS. Response to statin therapy 39 European ancestry severe statin myopathy cases, 40 European ancestry controls 67 European ancestry severe statin myopathy cases, 42 European ancestry controls Affymetrix [NR] 0 response to statin http://purl.obolibrary.org/obo/GO_0036273 GCST001192 Genome-wide genotyping array 2012-10-23 22911880 Boraska V 2012-08-22 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/22911880 Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits. Eating disorders Up to 2,567 European ancestry individuals Up to 767 European ancestry cases, up to 486 European ancestry controls Illumina [283744] 7 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST001644 Genome-wide genotyping array 2013-12-05 23776548 Sim X 2013-06-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/23776548 Genetic loci for retinal arteriolar microcirculation. Retinal arteriolar caliber 18,722 European ancestry individuals 3,939 European ancestry individuals Illumina [2137729] (imputed) 2 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST002071 Genome-wide genotyping array 2011-10-22 21980494 Germain M 2011-09-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/21980494 Genetics of venous thrombosis: insights from a new genome wide association study. Venous thromboembolism 1,542 European ancestry cases, 1,110 European ancestry controls NA Illumina [481002] 4 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST001253 Genome-wide genotyping array 2011-10-01 21777205 Dumitrescu L 2011-07-21 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/21777205 Evidence for age as a modifier of genetic associations for lipid levels. Lipid traits 282 European ancestry children, 66 African American children, 63 Hispanic children 1,627 European ancestry individuals, 1,478 African ancestry individuals, 1,443 Hispanic individuals Affymetrix [420005] 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST001170 Genome-wide genotyping array 2012-08-15 22705344 Sobrin L 2012-06-15 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/22705344 Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes. Age-related macular degeneration (choroidal neovascularisation) 1,775 European ancestry choroidal neovascularization cases, 4,134 European ancestry controls 4,515 European and unknown ancestry choroidal neovascularization cases, 15,240 European and unknown ancestry controls Affymetrix, Illumina [6036699] (imputed) 6 wet macular degeneration http://www.ebi.ac.uk/efo/EFO_0004683 GCST001579 Genome-wide genotyping array 2012-08-15 22705344 Sobrin L 2012-06-15 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/22705344 Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes. Age-related macular degeneration (geographic atrophy) 819 European ancestry geographic atrophy cases, 4,134 European ancestry controls NA Affymetrix, Illumina [6036699] (imputed) 9 atrophic macular degeneration http://www.ebi.ac.uk/efo/EFO_1001492 GCST001578 Genome-wide genotyping array 2012-08-30 22705344 Sobrin L 2012-06-15 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/22705344 Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes. Age-related macular degeneration (CNV vs. GA) 1,775 European ancestry choroidal neovascularization cases, 819 European ancestry geographic atrophy cases, 4,515 European and unknown ancestry choroidal neovascularization cases, 868 European and unknown ancestry geographic atrophy cases Affymetrix, Illumina [6036699] (imputed) 1 atrophic macular degeneration, wet macular degeneration http://www.ebi.ac.uk/efo/EFO_1001492, http://www.ebi.ac.uk/efo/EFO_0004683 GCST001577 Genome-wide genotyping array 2014-03-01 23937595 Al Safar HS 2013-08-13 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/23937595 A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family. Type 2 diabetes 66 Arab ancestry cases and 112 Arab ancestry controls from one extended family 116 Arab ancestry cases, 199 Arab ancestry controls Illumina [443502] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002123 Genome-wide genotyping array 2012-09-26 22828495 Brown AA 2012-07-24 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/22828495 Genetic variants affecting the neural processing of human facial expressions: evidence using a genome-wide functional imaging approach. Neural processing (facial expression) 246 European ancestry individuals 85 European ancestry individuals Affymetrix [549640] 0 facial neural processing http://www.ebi.ac.uk/efo/EFO_0004914 GCST001618 Genome-wide genotyping array 2013-07-27 23511034 Yang SK 2013-04-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/23511034 Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians. Ulcerative colitis 388 Korean ancestry cases, 739 Korean ancestry controls 810 Korean ancestry cases, 1709 Korean ancestry controls Illumina [581060] 1 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST001934 Genome-wide genotyping array 2013-07-27 23511034 Yang SK 2013-04-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/23511034 Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians. Ulcerative colitis 388 Korean ancestry cases, 739 Korean ancestry controls 417 Korean ancestry cases, 732 Korean ancestry controls Illumina [581060] 7 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST001938 Genome-wide genotyping array 2011-09-23 21871595 Day-Williams AG 2011-08-25 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21871595 A variant in MCF2L is associated with osteoarthritis. Osteoarthritis 3,177 European ancestry cases, 4,894 European ancestry controls 15,864 European ancestry cases, 19,610 European ancestry controls NR [7258070] (imputed) 1 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST001209 Genome-wide genotyping array 2011-01-12 21106707 Gu J 2010-11-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21106707 A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity. Response to bleomycin (chromatid breaks) 673 European ancestry individuals 834 European ancestry individuals Illumina [539437] 3 response to bleomycin, chromatid break measurement, response to antibiotic http://www.ebi.ac.uk/efo/EFO_0007592, http://www.ebi.ac.uk/efo/EFO_0007593, http://purl.obolibrary.org/obo/GO_0046677 GCST000882 Genome-wide genotyping array 2013-05-17 21886828 Wei W 2011-08-19 PLoS One www.ncbi.nlm.nih.gov/pubmed/21886828 Characterisation of genome-wide association epistasis signals for serum uric acid in human population isolates. Uric acid levels (SNP x SNP interaction) 1,201 European ancestry individuals 4,641 European ancestry individuals Illumina [293913] 0 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST001206 Genome-wide genotyping array 2012-09-20 22751097 Lu X 2012-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22751097 Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease. Coronary heart disease 1,515 Han Chinese ancestry cases, 5,019 Han Chinese ancestry controls 15,460 Han Chinese ancestry cases, 11,472 Han Chinese ancestry controls Affymetrix [~ 2200000] (imputed) 8 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001587 Genome-wide genotyping array 2011-01-15 21131975 Purdue MP 2010-12-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21131975 Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. Renal cell carcinoma 3,772 European ancestry cases, 8,505 European ancestry controls 2,198 European ancestry cases, 4,918 European ancestry controls Illumina [586069] 4 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST000907 Genome-wide genotyping array 2014-02-25 23935489 McLaren PJ 2013-07-25 PLoS Pathog www.ncbi.nlm.nih.gov/pubmed/23935489 Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls. HIV-1 susceptibility 6,334 European ancestry cases, 7,247 European ancestry controls NA Affymetrix, Illumina [~ 8000000] (imputed) 1 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST002101 Genome-wide genotyping array 2012-02-23 22286173 Low SK 2012-01-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22286173 Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA. Intracranial aneurysm 1,383 Japanese ancestry cases, 5,484 Japanese ancestry controls 1,048 Japanese ancestry cases, 7,212 Japanese ancestry controls Illumina [565149] 4 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST001388 Genome-wide genotyping array 2015-05-19 21685187 Siedlinski M 2011-06-16 Thorax www.ncbi.nlm.nih.gov/pubmed/21685187 Genome-wide association study of smoking behaviours in patients with COPD. Age at smoking initiation in chronic obstructive pulmonary disease 3,397 European ancestry cases NA Illumina [~ 6300000] (imputed) 21 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST001113 Genome-wide genotyping array 2015-05-19 21685187 Siedlinski M 2011-06-16 Thorax www.ncbi.nlm.nih.gov/pubmed/21685187 Genome-wide association study of smoking behaviours in patients with COPD. Smoking cessation in chronic obstructive pulmonary disease 1,907 European ancestry former smoker cases, 1,164 European ancestry current smoker cases NA Illumina [~ 6300000] (imputed) 8 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST001108 Genome-wide genotyping array 2015-05-18 21685187 Siedlinski M 2011-06-16 Thorax www.ncbi.nlm.nih.gov/pubmed/21685187 Genome-wide association study of smoking behaviours in patients with COPD. Current cigarettes per day in chronic obstructive pulmonary disease 1,113 European ancestry cases NA Illumina [~ 6300000] (imputed) 7 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST001111 Genome-wide genotyping array 2015-05-18 21685187 Siedlinski M 2011-06-16 Thorax www.ncbi.nlm.nih.gov/pubmed/21685187 Genome-wide association study of smoking behaviours in patients with COPD. Lifetime average cigarettes per day in chronic obstructive pulmonary disease 3,440 European ancestry cases NA Illumina [~ 6300000] (imputed) 11 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST001112 Genome-wide genotyping array 2012-05-04 22479346 Yang HC 2012-03-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/22479346 Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study. Hypertension 400 Han Chinese ancestry cases, 400 Han Chinese ancestry controls 315 Han Chinese ancestry individuals, 1,999 European ancestry cases, 3,004 European ancestry controls Illumina [475157] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST001467 Genome-wide genotyping array 2012-09-20 22797724 Shiraishi K 2012-07-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22797724 A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population. Lung adenocarcinoma 1,695 Japanese ancestry cases, 5,333 Japanese ancestry controls 4,334 Japanese ancestry cases, 8,202 Japanese ancestry controls Illumina [538166] 4 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST001609 Genome-wide genotyping array 2013-02-12 23128233 Jostins L 2012-11-01 Nature www.ncbi.nlm.nih.gov/pubmed/23128233 Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Crohn's disease Up to 12,924 European ancestry cases, up to 21,442 European ancestry controls Up to 25,683 European ancestry cases, up to 17,015 European ancestry controls Affymetrix, Illumina [1230000] (imputed) 30 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST001729 Genome-wide genotyping array 2013-02-12 23128233 Jostins L 2012-11-01 Nature www.ncbi.nlm.nih.gov/pubmed/23128233 Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Ulcerative colitis Up to 12,924 European ancestry cases, up to 21,442 European ancestry controls Up to 25,683 European ancestry cases, up to 17,015 European ancestry controls Affymetrix, Illumina [1230000] (imputed) 23 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST001728 Genome-wide genotyping array 2013-02-12 23128233 Jostins L 2012-11-01 Nature www.ncbi.nlm.nih.gov/pubmed/23128233 Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Inflammatory bowel disease 12,924 European ancestry cases, 21,442 European ancestry controls 25,683 European ancestry cases, 17,015 European ancestry controls Affymetrix, Illumina [1230000] (imputed) 110 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST001725 Genome-wide genotyping array 2013-06-26 23532257 Ma RC 2013-03-27 Diabetologia www.ncbi.nlm.nih.gov/pubmed/23532257 Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Type 2 diabetes 684 Han Chinese ancestry cases, 955 Han Chinese ancestry controls 18,954 East Asian ancestry cases, 18,029 East Asian ancestry controls, 794 Malay ancestry cases, 1,204 Malay ancestry controls, 977 Indian ancestry cases, 1,169 Indian ancestry controls, 8,130 European ancestry cases, 38,987 European ancestry controls Illumina [2925090] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001919 Genome-wide genotyping array 2012-08-14 22832960 Service SK 2012-05-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/22832960 A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales. Temperament Up to 12,433 European ancestry individuals NA Affymetrix, Illumina [1252222] (imputed) 16 temperament and character inventory http://www.ebi.ac.uk/efo/EFO_0004825 GCST001531 Genome-wide genotyping array 2012-09-12 22785395 Gaj P 2012-07-11 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/22785395 Identification of a late onset Alzheimer's disease candidate risk variant at 9q21.33 in Polish patients. Alzheimer's disease 141 European ancestry cases, 141 European ancestry controls NA Affymetrix [NR] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001602 Genome-wide genotyping array 2013-12-10 23740775 Xie G 2013-09-01 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/23740775 Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis. Wegener's granulomatosis 459 European ancestry cases, 1,503 European ancestry controls 291 European ancestry cases, 317 European ancestry controls Illumina [287802] 5 Granulomatosis with Polyangiitis http://www.ebi.ac.uk/efo/EFO_0005297 GCST002160 Genome-wide genotyping array 2013-12-10 23740775 Xie G 2013-09-01 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/23740775 Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis. Wegener's granulomatosis 459 European ancestry cases, 1,503 European ancestry controls 528 European ancestry cases, 1,228 European ancestry controls Illumina [287802] 1 Granulomatosis with Polyangiitis http://www.ebi.ac.uk/efo/EFO_0005297 GCST002159 Genome-wide genotyping array 2012-10-24 22907730 Ji Y 2012-08-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/22907730 Pharmacogenomics of selective serotonin reuptake inhibitor treatment for major depressive disorder: genome-wide associations and functional genomics. Response to antidepressants Up to 499 European ancestry cases 1,207 European ancestry cases Illumina [532877] 0 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST001641 Genome-wide genotyping array 2013-12-03 23755828 Perera MA 2013-06-05 Lancet www.ncbi.nlm.nih.gov/pubmed/23755828 Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study. Warfarin maintenance dose 533 African American individuals 432 African American individuals Illumina [3044177] (imputed) 1 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST002061 Genome-wide genotyping array 2012-09-08 22754043 Byrne EM 2012-07-01 Sleep www.ncbi.nlm.nih.gov/pubmed/22754043 A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor. Insomnia (caffeine-induced) 2,402 European ancestry individuals from 1,470 families NA Illumina [2380486] (imputed) 9 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST001586 Genome-wide genotyping array 2013-08-06 23509962 Greliche N 2013-03-20 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/23509962 A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis. Venous thromboembolism (SNP x SNP interaction) 411 European ancestry cases, 1,228 European ancestry controls 1,542 European ancestry cases, 1,110 European ancestry controls Illumina [291872] 37 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST001913 Genome-wide genotyping array 2013-04-11 23314186 Crosslin DR 2013-03-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23314186 Genetic variation associated with circulating monocyte count in the eMERGE Network. Monocyte count 9,849 European ancestry individuals, 894 African ancestry individuals, 271 individuals NA Illumina [NR] 6 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST001887 Genome-wide genotyping array 2012-04-24 22455414 Tekola Ayele F 2012-03-29 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/22455414 HLA class II locus and susceptibility to podoconiosis. Podoconiosis 194 African ancestry cases, 203 African ancestry controls 202 African ancestry family trios Illumina [551840] 0 podoconiosis http://www.ebi.ac.uk/efo/EFO_0004712 GCST001464 Genome-wide genotyping array 2012-08-15 22581228 Manning AK 2012-05-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22581228 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Fasting blood insulin (BMI interaction) Up to 51,750 European ancestry individuals Up to 33,823 European ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 20 body mass index, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004466 GCST001526 Genome-wide genotyping array 2012-08-15 22581228 Manning AK 2012-05-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22581228 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Fasting blood glucose (BMI interaction) Up to 58,074 European ancestry individuals Up tp 38,422 European ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 33 body mass index, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004465 GCST001527 Genome-wide genotyping array 2018-01-25 22581228 Manning AK 2012-05-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22581228 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Fasting blood insulin Up to 51,750 European ancestry individuals Up to 33,823 European ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 10 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST005185 Genome-wide genotyping array 2018-01-25 22581228 Manning AK 2012-05-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22581228 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Fasting blood glucose Up to 58,074 European ancestry individuals Up tp 38,422 European ancestry individuals Affymetrix, Illumina [~ 2400000] (imputed) 33 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST005186 Genome-wide genotyping array 2010-06-13 20453842 Stahl EA 2010-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20453842 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Rheumatoid arthritis 5,539 European ancestry cases, 20,169 European ancestry controls 6,768 European ancestry cases, 8,806 European ancestry controls Affymetrix, Illumina [~ 2716259] (imputed) 29 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000679 Genome-wide genotyping array 2012-03-14 22331829 Chasman DI 2012-02-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/22331829 Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial. Response to statins (LDL cholesterol change) 6,989 European ancestry individuals NA Illumina [814418] 8 response to statin, LDL cholesterol change measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0007804 GCST001408 Genome-wide genotyping array 2011-09-22 21862451 Benyamin B 2011-08-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21862451 GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors. Butyrylcholinesterase levels 6,879 European ancestry adult individuals 1,260 European ancestry adult individuals, 652 European ancestry adolescent individuals Illumina [2383238] (imputed) 3 butyrylcholinesterase measurement http://www.ebi.ac.uk/efo/EFO_0004571 GCST001207 Genome-wide genotyping array 2012-09-14 22780124 Lind PA 2012-07-11 Addict Biol www.ncbi.nlm.nih.gov/pubmed/22780124 Genome-wide association study of a quantitative disordered gambling trait. Gambling 1,312 European ancestry twins from 894 families NA Illumina [2373249] (imputed) 5 gambling behaviour http://www.ebi.ac.uk/efo/EFO_0004699 GCST001601 Genome-wide genotyping array 2012-09-15 22911860 Hernandez DG 2012-07-24 PLoS One www.ncbi.nlm.nih.gov/pubmed/22911860 Genome wide assessment of young onset Parkinson's disease from Finland. Parkinson's disease 387 European ancestry cases, 496 European ancestry controls NA Illumina [5854841] (imputed) 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST001617 Genome-wide genotyping array 2011-08-12 21779181 Gorlova O 2011-07-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21779181 Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. Systemic sclerosis 2,296 European ancestry cases, 5,172 European ancestry controls 3,175 European ancestry cases, 4,210 European ancestry controls Illumina [NR] (imputed) 6 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST001160 Genome-wide genotyping array 2011-08-12 21779181 Gorlova O 2011-07-14 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21779181 Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. Systemic sclerosis 2,296 European ancestry cases, 5,172 European ancestry controls 3,175 European ancestry cases, 4,210 European ancestry controls Illumina [NR] (imputed) 12 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST001156 Genome-wide genotyping array 2012-11-05 22960237 Han Y 2012-08-31 Bone www.ncbi.nlm.nih.gov/pubmed/22960237 Bivariate genome-wide association study suggests fatty acid desaturase genes and cadherin DCHS2 for variation of both compressive strength index and appendicular lean mass in males. Comprehensive strength and appendicular lean mass 825 Chinese ancestry female individuals, 802 Chinese ancestry male individuals 1,059 European ancestry male individuals, 2,227 European ancestry female individuals Affymetrix [701525] 2 comprehensive strength index, muscle measurement http://www.ebi.ac.uk/efo/EFO_0004979, http://www.ebi.ac.uk/efo/EFO_0004515 GCST001656 Genome-wide genotyping array 2010-04-12 20332263 Azzato EM 2010-03-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/20332263 A genome-wide association study of prognosis in breast cancer. Breast cancer (prognosis) 1,145 female individuals 4,335 European ancestry female individuals Illumina [528252] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST000637 Genome-wide genotyping array 2014-02-21 23932459 Yao TC 2013-08-06 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/23932459 Genome-wide association study of lung function phenotypes in a founder population. Pulmonary function 1,144 Hutterite individuals NA Affymetrix [246010] 7 pulmonary function measurement, forced expiratory volume, FEV/FEC ratio, vital capacity http://www.ebi.ac.uk/efo/EFO_0003892, http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0004713, http://www.ebi.ac.uk/efo/EFO_0004312 GCST002113 Genome-wide genotyping array 2010-05-05 20383145 Chambers JC 2010-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20383145 Genetic loci influencing kidney function and chronic kidney disease. Creatinine levels 23,812 European ancestry individuals 16,626 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2600000] (imputed) 5 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST000651 Genome-wide genotyping array 2013-12-05 23749188 Tan DE 2013-06-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23749188 Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population. B cell non-Hodgkin lymphoma 253 Singaporean Chinese ancestry cases, 1,438 Singaporean Chinese ancestry controls 1,175 Han Chinese ancestry cases, 5,492 Han Chinese ancestry controls Illumina [550946] 1 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST002066 Genome-wide genotyping array 2011-08-18 21785125 Traglia M 2011-07-25 J Med Genet www.ncbi.nlm.nih.gov/pubmed/21785125 Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations. Hepcidin levels 1,657 Val Borbera (founder/genetic isolate) individuals NA Illumina [343866] 8 serum hepcidin measurement http://www.ebi.ac.uk/efo/EFO_0004504 GCST001174 Genome-wide genotyping array 2011-01-10 21149285 Ozeki T 2010-12-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21149285 Genome-wide association study identifies HLA-A*3101 allele as a genetic risk factor for carbamazepine-induced cutaneous adverse drug reactions in Japanese population. Adverse response to carbamazepine 53 Japanese ancestry cases, 881 Japanese ancestry controls 23 Japanese ancestry cases, 44 Japanese ancestry controls Illumina [444823] 1 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST000912 Genome-wide genotyping array 2011-09-02 21782286 Walter S 2011-07-20 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/21782286 A genome-wide association study of aging. Aging (time to death) 25,007 European ancestry individuals 10,411 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 3 longevity, obsolete aging http://www.ebi.ac.uk/efo/EFO_0004300, http://purl.obolibrary.org/obo/GO_0007568 GCST001167 Genome-wide genotyping array 2011-09-02 21782286 Walter S 2011-07-20 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/21782286 A genome-wide association study of aging. Aging (time to event) 16,995 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST001166 Genome-wide genotyping array 2012-04-25 22446961 Lee YC 2012-03-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22446961 Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis. Kawasaki disease 622 Han Chinese ancestry cases, 1,107 Han Chinese ancestry controls 261 Han Chinese ancestry cases, 550 Han Chinese ancestry controls Affymetrix [716935] 6 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST001456 Genome-wide genotyping array 2011-12-08 22010049 Middelberg RP 2011-11-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22010049 Loci affecting gamma-glutamyl transferase in adults and adolescents show age × SNP interaction and cardiometabolic disease associations. Gamma glutamyl transferase levels 12,526 European ancestry individuals NA Illumina [2380486] (imputed) 4 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST001307 Genome-wide genotyping array 2011-06-01 21572414 Suhre K 2011-05-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21572414 A genome-wide association study of metabolic traits in human urine. Urinary metabolites 862 European ancestry male individuals 1,862 European ancestry individuals Affymetrix [645249] 5 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST001073 Genome-wide genotyping array 2011-08-19 21795503 Alkelai A 2011-07-27 FASEB J www.ncbi.nlm.nih.gov/pubmed/21795503 Identification of new schizophrenia susceptibility loci in an ethnically homogeneous, family-based, Arab-Israeli sample. Schizophrenia 189 Arab-Israeli founder individuals from 57 families 627 European ancestry cases, 541 European ancestry controls Illumina [307472] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001176 Genome-wide genotyping array 2009-01-21 19122664 Silverberg MS 2009-01-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19122664 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. Ulcerative colitis 1,022 European ancestry cases, 2,503 European ancestry controls 1,387 European ancestry cases, 1,115 European ancestry controls Illumina [280748] 12 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000311 Genome-wide genotyping array 2012-09-20 22794196 Lu Y 2012-07-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/22794196 Genome-wide association study for ovarian cancer susceptibility using pooled DNA. Ovarian cancer 342 European ancestry cases, 643 European ancestry controls 4,651 European ancestry cases, 6,966 European ancestry controls Illumina [914948] 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST001589 Genome-wide genotyping array 2011-09-14 21812969 Liu X 2011-08-03 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/21812969 Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population. Parkinson's disease 268 Ashkenazi Jewish cases, 178 Ashkenazi Jewish controls 1,782 European ancestry cases, 1,658 European ancestry controls Illumina [525124] 3 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST001189 Genome-wide genotyping array 2010-06-02 20445134 Smith NL 2010-05-05 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20445134 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. Heart failure 20,926 European ancestry individuals, 2,895 African ancestry individuals NA Affymetrix, Illumina [2478304] (imputed) 16 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST000675 Genome-wide genotyping array 2011-05-25 21533074 Smedby KE 2011-04-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21533074 GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma. Follicular lymphoma 379 European ancestry cases, 791 European ancestry controls 1,049 European ancestry cases, 3,952 European ancestry controls Illumina [298168] 1 neoplasm of mature B-cells http://www.ebi.ac.uk/efo/EFO_0000096 GCST001051 Genome-wide genotyping array 2011-09-03 21804547 Dobbins SE 2011-07-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21804547 Common variation at 10p12.31 near MLLT10 influences meningioma risk. Meningioma 859 European ancestry cases, 704 European ancestry controls 774 European ancestry cases, 1,764 European ancestry controls Illumina [270875] 1 meningioma http://purl.obolibrary.org/obo/MONDO_0016642 GCST001184 Genome-wide genotyping array 2010-06-14 20460622 Seshadri S 2010-05-12 JAMA www.ncbi.nlm.nih.gov/pubmed/20460622 Genome-wide analysis of genetic loci associated with Alzheimer disease. Alzheimer's disease 973 incident AD cases, 2,033 prevalent AD cases, 22,604 controls of European and Hispanic ancestry 6,505 European ancestry cases, 13,532 European ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000682 Genome-wide genotyping array 2014-07-23 24324551 Deng X 2013-11-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324551 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. Parasitemia in Tripanosoma cruzi seropositivity 580 Brazilian ancestry individuals NA Affymetrix [5486770] (imputed) 24 parasitemia measurement http://www.ebi.ac.uk/efo/EFO_0005528 GCST002282 Genome-wide genotyping array 2014-07-23 24324551 Deng X 2013-11-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324551 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. QRS duration in Tripanosoma cruzi seropositivity 580 Brazilian ancestry individuals NA Affymetrix [5486770] (imputed) 38 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST002284 Genome-wide genotyping array 2014-07-23 24324551 Deng X 2013-11-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324551 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. Chagas cardiomyopathy in Tripanosoma cruzi seropositivity 207 Brazilian ancestry cases, 306 Brazilian ancestry controls NA Affymetrix [5486770] (imputed) 18 Chagas cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0005529 GCST002285 Genome-wide genotyping array 2014-07-23 24324551 Deng X 2013-11-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324551 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. Antibody status in Tripanosoma cruzi seropositivity 580 Brazilian ancestry individuals NA Affymetrix [5486770] (imputed) 20 antibody measurement http://www.ebi.ac.uk/efo/EFO_0004556 GCST002280 Genome-wide genotyping array 2014-07-23 24324551 Deng X 2013-11-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324551 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. PR interval in Tripanosoma cruzi seropositivity 580 Brazilian ancestry individuals NA Affymetrix [5486770] (imputed) 102 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST002279 Genome-wide genotyping array 2014-07-23 24324551 Deng X 2013-11-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324551 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. QT interval in Tripanosoma cruzi seropositivity 580 Brazilian ancestry individuals NA Affymetrix [5486770] (imputed) 14 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST002278 Genome-wide genotyping array 2014-07-23 24324551 Deng X 2013-11-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324551 Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. Ejection fraction in Tripanosoma cruzi seropositivity 580 Brazilian ancestry individuals NA Affymetrix [5486770] (imputed) 25 ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0005527 GCST002281 Genome-wide genotyping array 2012-02-23 22286212 Urayama KY 2012-01-27 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/22286212 Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups. Hodgkin's lymphoma 1,200 European ancestry cases, 6,417 European ancestry controls 563 European ancestry cases, 613 European ancestry controls Illumina [502514] 4 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST001387 Genome-wide genotyping array 2013-09-18 23636237 Tanaka T 2013-05-01 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/23636237 Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake. Dietary macronutrient intake 37,537 European ancestry individuals 33,533 European ancestry individuals Affymetrix, Illumina [2500000] (imputed) 6 energy intake http://www.ebi.ac.uk/efo/EFO_0003939 GCST001988 Genome-wide genotyping array 2013-09-17 23636237 Tanaka T 2013-05-01 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/23636237 Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake. Dietary macronutrient intake 37,537 European ancestry individuals 41,257 European ancestry individuals Affymetrix, Illumina [2500000] (imputed) 1 energy intake http://www.ebi.ac.uk/efo/EFO_0003939 GCST001989 Genome-wide genotyping array 2010-06-08 20452100 Kramer PL 2010-05-06 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/20452100 Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study. Alzheimer's disease 185 European ancestry low NFT individuals, 114 European ancestry high NFT individuals NA Illumina [292175] 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000676 Genome-wide genotyping array 2010-08-30 20622879 Mizuki N 2010-07-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20622879 Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci. Behcet's disease 611 Japanese ancestry cases, 737 Japanese ancestry controls 119 Korean ancestry cases, 140 Korean ancestry controls, 1,215 Turkish cases, 1,279 Turkish controls Affymetrix [320438] 2 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST000728 Genome-wide genotyping array 2010-09-14 20691247 Verweij KJ 2010-08-04 Biol Psychol www.ncbi.nlm.nih.gov/pubmed/20691247 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. Personality dimensions 5,117 European ancestry individuals from 2567 families NA Affymetrix, Illumina [1252387] (imputed) 7 personality trait http://www.ebi.ac.uk/efo/EFO_0004365 GCST000754 Genome-wide genotyping array 2014-07-23 24262325 Dichgans M 2013-11-21 Stroke www.ncbi.nlm.nih.gov/pubmed/24262325 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Coronary artery disease 33,398 cases, 75,726 controls NA Illumina [575000] (imputed) 23 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST002289 Genome-wide genotyping array 2014-07-23 24262325 Dichgans M 2013-11-21 Stroke www.ncbi.nlm.nih.gov/pubmed/24262325 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Ischemic stroke 12,389 cases, 62,004 controls NA Affymetrix, Illumina [~ 2500000] (imputed) 6 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST002286 Genome-wide genotyping array 2014-07-23 24262325 Dichgans M 2013-11-21 Stroke www.ncbi.nlm.nih.gov/pubmed/24262325 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Large artery stroke 2,167 cases, 49,159 controls NA Affymetrix, Illumina [~ 2400000] (imputed) 9 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST002288 Genome-wide genotyping array 2014-07-23 24262325 Dichgans M 2013-11-21 Stroke www.ncbi.nlm.nih.gov/pubmed/24262325 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Coronary artery disease or ischemic stroke 12,389 Ischemic stroke cases, 22,233 Coronary artery disease cases, ~ 88,766 controls NA Affymetrix, Illumina [up to 2500000] (imputed) 14 stroke, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0001645 GCST002287 Genome-wide genotyping array 2014-07-23 24262325 Dichgans M 2013-11-21 Stroke www.ncbi.nlm.nih.gov/pubmed/24262325 Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants. Coronary artery disease or large artery stroke 2,167 Large artery stroke cases, 22,233 Coronary artery disease cases, ~ 75,921 controls NA Affymetrix, Illumina [up to 2500000] (imputed) 17 large artery stroke, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0005524, http://www.ebi.ac.uk/efo/EFO_0001645 GCST002290 Genome-wide genotyping array 2014-03-24 24080187 Guffanti G 2013-09-08 Psychoneuroendocrinology www.ncbi.nlm.nih.gov/pubmed/24080187 Genome-wide association study implicates a novel RNA gene, the lincRNA AC068718.1, as a risk factor for post-traumatic stress disorder in women. Post-traumatic stress disorder 81 African American female cases, 261 African American female controls, 10 European ancestry female cases, 35 European ancestry female controls, 3 female cases, 22 female controls 578 European ancestry female cases, 1,963 European ancestry female controls Illumina [688890] 0 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST002171 Genome-wide genotyping array 2011-12-03 22068335 Mitchell GF 2011-11-08 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/22068335 Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium. Aortic stiffness 4,216 Sardinian individuals, 20,634 European ancestry individuals 5,306 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 1 carotid-femoral pulse wave velocity http://www.ebi.ac.uk/efo/EFO_0004724 GCST001317 Genome-wide genotyping array 2015-04-02 25006744 Castaldi PJ 2014-07-09 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/25006744 Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns. Local histogram emphysema pattern 3,732 European ancestry smoker individuals, 2,724 European ancestry chronic obstructive pulmonary disease smoker cases, 2,372 African American smoker individuals, 786 African American chronic obstructive pulmonary disease smoker cases NA Illumina [6942916] (imputed) 25 emphysema pattern measurement http://www.ebi.ac.uk/efo/EFO_0005850 GCST002525 Genome-wide genotyping array 2014-03-20 23936387 Ostensson M 2013-08-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/23936387 A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. Celiac disease 206 European ancestry trios NA Illumina [944512] (imputed) 15 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST002112 Genome-wide genotyping array 2014-04-15 24182552 Matteini AM 2013-10-29 Cytokine www.ncbi.nlm.nih.gov/pubmed/24182552 Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults. Inflammatory biomarkers 4,443 European ancestry older adult individuals NA Illumina [2543887] (imputed) 3 interleukin-1 beta measurement, interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004812, http://www.ebi.ac.uk/efo/EFO_0004754 GCST002255 Genome-wide genotyping array 2012-07-19 22673310 Liao M 2012-07-07 Genes Immun www.ncbi.nlm.nih.gov/pubmed/22673310 Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population. IgG levels 1,999 Chinese ancestry male individuals 1,496 Chinese ancestry male individuals Illumina [1940243] (imputed) 1 serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0004565 GCST001600 Genome-wide genotyping array 2012-09-27 22808956 Lyons PA 2012-07-19 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/22808956 Genetically distinct subsets within ANCA-associated vasculitis. Antineutrophil cytoplasmic antibody-associated vasculitis 914 European ancestry cases, 5,259 European ancestry controls 1,454 European ancestry cases, 1,666 European ancestry controls Affymetrix [NR] 18 anti-neutrophil antibody associated vasculitis http://www.ebi.ac.uk/efo/EFO_0004826 GCST001613 Genome-wide genotyping array 2014-07-22 24234648 Goris A 2013-11-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24234648 No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. Multiple sclerosis or amyotrophic lateral sclerosis 4,088 Multiple sclerosis cases, 3,762 Amyotrophic lateralsclerosis cases, 12,030 controls NA NR [5440446] (imputed) 1 amyotrophic lateral sclerosis, multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0004976, http://purl.obolibrary.org/obo/MONDO_0005301 GCST002274 Genome-wide genotyping array 2011-12-02 22037552 Yue WH 2011-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22037552 Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2. Schizophrenia 746 Han Chinese ancestry cases, 1,599 Han Chinese ancestry controls 4,027 Han Chinese ancestry cases, 5,603 Han Chinese ancestry controls Illumina [493203] 2 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001299 Genome-wide genotyping array 2011-06-01 21565293 Teumer A 2011-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/21565293 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. Thyroid volume 3,620 European ancestry individuals 1,290 European ancestry individuals Affymetrix [2748910] (imputed) 8 thyroid volume http://www.ebi.ac.uk/efo/EFO_0004865 GCST001069 Genome-wide genotyping array 2014-12-10 25015694 Kolek MJ 2014-06-06 Am J Cardiol www.ncbi.nlm.nih.gov/pubmed/25015694 A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation. Response to rate control therapy in atrial fibrillation 95 non-responders, 190 responders 130 non-responders, 157 responders Illumina [6100000] (imputed) 0 response to rate control therapy http://www.ebi.ac.uk/efo/EFO_0005768 GCST002473 Genome-wide genotyping array 2013-11-07 23666239 Chung CC 2013-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23666239 Meta-analysis identifies four new loci associated with testicular germ cell tumor. Testicular germ cell tumor 582 European ancestry male cases, 1,056 European ancestry male controls 3,560 European ancestry male cases, 8,510 European ancestry male controls Illumina [NR] 11 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST002023 Genome-wide genotyping array 2013-01-23 23142968 Betcheva ET 2012-11-07 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23142968 Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene. Schizophrenia 188 European ancestry cases, 376 European ancestry controls 99 European ancestry cases, 328 European ancestry controls Illumina [495089] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001733 Genome-wide genotyping array 2014-04-26 24165912 He J 2013-10-28 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24165912 Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese. Blood pressure measurement (cold pressor test) 1,881 Han Chinese ancestry individuals 698 Han Chinese ancestry individuals Affymetrix [2216774] (imputed) 7 blood pressure, response to cold pressor test http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0005404 GCST002247 Genome-wide genotyping array 2014-04-26 24165912 He J 2013-10-28 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24165912 Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese. Blood pressure measurement (high sodium and potassium intervention) 1,836 Han Chinese ancestry individuals 654 Han Chinese ancestry individuals Affymetrix [2216774] (imputed) 13 blood pressure, response to high sodium diet, response to dietary potassium supplementation http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0005401, http://www.ebi.ac.uk/efo/EFO_0005403 GCST002252 Genome-wide genotyping array 2014-04-26 24165912 He J 2013-10-28 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24165912 Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese. Blood pressure measurement (low sodium intervention) 1,850 Han Chinese ancestry individuals 660 Han Chinese ancestry individuals Affymetrix [2216774] (imputed) 10 blood pressure, response to low sodium diet http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0005402 GCST002250 Genome-wide genotyping array 2014-04-26 24165912 He J 2013-10-28 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24165912 Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese. Blood pressure measurement (high sodium intervention) 1,840 Han Chinese ancestry individuals 659 Han Chinese ancestry individuals Affymetrix [2216774] (imputed) 11 blood pressure, response to high sodium diet http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0005401 GCST002249 Genome-wide genotyping array 2012-09-12 22792071 Zheng HF 2012-07-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22792071 WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk. Bone mineral density 5,672 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST001595 Genome-wide genotyping array 2012-09-12 22792071 Zheng HF 2012-07-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22792071 WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk. Cortical thickness 5,878 European ancestry individuals 1,032 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST001593 Genome-wide genotyping array 2013-11-14 23677057 Kim JJ 2013-05-16 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23677057 Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysis. Coronary arterial lesions in patients with Kawasaki disease 17 Korean ancestry cases, 123 Korean ancestry controls 32 Korean ancestry cases, 191 Korean ancestry controls Affymetrix [652397] 1 coronary aneurysm http://www.ebi.ac.uk/efo/EFO_1000881 GCST002026 Genome-wide genotyping array 2014-03-01 23836404 Shulman JM 2013-09-01 JAMA Neurol www.ncbi.nlm.nih.gov/pubmed/23836404 Genetic susceptibility for Alzheimer disease neuritic plaque pathology. Alzheimer's disease (neuritic plaque pathology) 651 European and unknown ancestry individuals 114 individuals Affymetrix [2465581] (imputed) 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002161 Genome-wide genotyping array 2012-01-18 22158537 Cho YS 2011-12-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22158537 Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Type 2 diabetes 5,999 East Asian ancestry cases, 9,001 East Asian ancestry controls, 794 Malay ancestry cases, 1,240 Malay ancestry controls, 159 Filipino ancestry cases, 1,624 Filipino ancestry controls 18,127 East Asian ancestry cases, 17,746 East Asian ancestry controls Affymetrix, Illumina [2626356] (imputed) 10 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001351 Genome-wide genotyping array 2014-03-11 23945395 Hara K 2013-08-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23945395 Genome-wide association study identifies three novel loci for type 2 diabetes. Type 2 diabetes 5,976 Japanese ancestry cases, 20,829 Japanese ancestry controls 24,416 East Asian ancestry cases, 13,985 East Asian ancestry controls Illumina [6209637] (imputed) 16 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002128 Genome-wide genotyping array 2013-08-21 23388002 Thanassoulis G 2013-02-17 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/23388002 Genetic associations with valvular calcification and aortic stenosis. Mitral annular calcification 3,795 European ancestry individuals 745 European ancestry individuals, 2,497 African American individuals, 2,027 Hispanic individuals, 774 Chinese ancestry individuals Affymetrix, Illumina [> 2500000] (imputed) 0 mitral annular calcification http://www.ebi.ac.uk/efo/EFO_0005262 GCST001864 Genome-wide genotyping array 2013-08-21 23388002 Thanassoulis G 2013-02-17 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/23388002 Genetic associations with valvular calcification and aortic stenosis. Aortic-valve calcification 6,942 European ancestry individuals 745 European ancestry individuals, 2,497 African American individuals, 2,027 Hispanic individuals, 774 Chinese ancestry individuals Affymetrix, Illumina [> 2500000] (imputed) 1 aortic valve calcification http://www.ebi.ac.uk/efo/EFO_0005239 GCST001865 Genome-wide genotyping array 2013-12-20 23793441 Davis MF 2013-06-21 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23793441 Parkinson disease loci in the mid-western Amish. Parkinson's disease 31 Amish cases, 767 Amish controls NA Affymetrix [622812] 3 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST002077 Genome-wide genotyping array 2010-09-11 20676096 Zhang H 2010-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20676096 Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers. Hepatocellular carcinoma 348 Chinese ancestry cases, 359 Chinese ancestry controls 2,121 Chinese ancestry cases, 1,748 Chinese ancestry controls Affymetrix [294566] 1 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST000752 Genome-wide genotyping array 2014-02-06 23829686 Ding L 2013-07-05 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/23829686 Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations. Asthma (childhood onset) 429 European ancestry affected offspring trios 52 African American affected offspring trios, 46 Hispanic affected offspring trios Affymetrix [786195] 19 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST002088 Genome-wide genotyping array 2010-09-22 20711174 Hor H 2010-08-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20711174 Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy. Narcolepsy 562 European ancestry cases, 702 European ancestry controls 370 cases, 495 controls Affymetrix [392949] 2 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST000771 Genome-wide genotyping array 2014-01-10 23827383 Cadby G 2013-07-01 Lung Cancer www.ncbi.nlm.nih.gov/pubmed/23827383 A genome-wide association study for malignant mesothelioma risk. Malignant mesothelioma 428 European ancestry cases, 2,047 European ancestry controls 392 European ancestry cases, 367 European ancestry controls Illumina [2508203] (imputed) 0 mesothelioma http://www.ebi.ac.uk/efo/EFO_0000588 GCST002085 Genome-wide genotyping array 2014-01-09 23817569 Hinds DA 2013-06-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23817569 A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. Self-reported allergy 53,862 European ancestry individuals NA Illumina [2400000] (imputed) 35 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST002083 Genome-wide genotyping array 2012-08-10 22719876 Kawaguchi T 2012-06-14 PLoS One www.ncbi.nlm.nih.gov/pubmed/22719876 Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese. Nonalcoholic fatty liver disease 529 Japanese ancestry cases, 932 Japanese ancestry controls NA Illumina [484751] 5 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST001576 Genome-wide genotyping array 2013-02-14 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Waist-to-hip circumference ratio (ever vs never smoking interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 smoking behaviour measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004343 GCST001754 Genome-wide genotyping array 2013-02-14 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Body mass index (alcohol intake interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 alcohol consumption measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004340 GCST001753 Genome-wide genotyping array 2017-08-24 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Body mass index (dietary energy interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 diet measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004587 Genome-wide genotyping array 2017-08-23 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Body mass index (recreational physical activity interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 physical activity measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004580 Genome-wide genotyping array 2017-08-24 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Body mass index (ever vs never smoking interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 smoking behaviour measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004586 Genome-wide genotyping array 2017-08-23 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Body mass index (smoking years interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 smoking behaviour measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004340 GCST004581 Genome-wide genotyping array 2017-08-23 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Waist-to-hip circumference ratio (dietary energy interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 diet measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004343 GCST004582 Genome-wide genotyping array 2017-08-23 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Waist-to-hip circumference ratio (smoking years interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 smoking behaviour measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0004343 GCST004584 Genome-wide genotyping array 2017-08-23 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Waist-to-hip circumference ratio (recreational physical activity interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 2 physical activity measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004343 GCST004583 Genome-wide genotyping array 2017-08-23 23192594 Velez Edwards DR 2012-11-29 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23192594 Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study. Waist-to-hip circumference ratio (alcohol intake interaction) 8,203 African American females, 3,484 Hispanic females NA Affymetrix [706791] 3 alcohol consumption measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004343 GCST004579 Genome-wide genotyping array 2010-08-17 20613766 Akiyama K 2010-07-08 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20613766 Genome-wide association study to identify genetic variants present in Japanese patients harboring intracranial aneurysms. Intracranial aneurysm 288 Japanese ancestry cases, 194 Japanese ancestry controls 739 Japanese ancestry cases, 659 Japanese ancestry controls Illumina [250507] 0 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST000723 Genome-wide genotyping array 2010-09-15 20694013 Davila S 2010-08-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20694013 Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. Meningococcal disease 475 European ancestry cases, 4,703 European ancestry controls 929 European ancestry cases, 1,351 European ancestry controls Illumina [518920] 1 meningococcal infection http://www.ebi.ac.uk/efo/EFO_0004249 GCST000762 Genome-wide genotyping array 2012-02-24 22245343 Meda SA 2012-01-08 Neuroimage www.ncbi.nlm.nih.gov/pubmed/22245343 A large scale multivariate parallel ICA method reveals novel imaging-genetic relationships for Alzheimer's disease in the ADNI cohort. Alzheimer's disease 367 European ancestry individuals with mild cognitive impairment, 181 European ancestry individuals with mild early-stage LOAD, 209 European ancestry controls NA Illumina [533872] 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001372 Genome-wide genotyping array 2012-08-16 22856363 Ousdal OT 2012-06-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/22856363 Associations between variants near a monoaminergic pathways gene (PHOX2B) and amygdala reactivity: a genome-wide functional imaging study. Amygdala reactivity 224 European ancestry individuals 50 European ancestry individuals, 13 African American individuals, 29 Asian ancestry individuals, 7 individuals Affymetrix [546381] 0 amygdala reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004550 GCST001551 Genome-wide genotyping array 2012-07-19 22661486 Ulmer M 2012-06-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/22661486 Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia. Central corneal thickness 973 European ancestry cases, 144 European ancestry controls NA Illumina [480304] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST001552 Genome-wide genotyping array 2012-03-30 22354554 Thompson SD 2012-02-21 Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/22354554 Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13. Arthritis (juvenile idiopathic) 814 European ancestry cases, 658 European ancestry controls, 2,400 controls 1,744 European ancestry cases, 7,010 European ancestry controls Affymetrix [561137] 4 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST001417 Genome-wide genotyping array 2011-12-14 22064162 Edwards AC 2011-11-05 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/22064162 Genome-wide association study of comorbid depressive syndrome and alcohol dependence. Depression and alcohol dependence 467 European ancestry cases, 407 European ancestry controls NA Illumina [876476] 8 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST001313 Genome-wide genotyping array 2012-03-09 22310351 Fernandez-Rozadilla C 2012-02-07 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/22310351 Pharmacogenomics in colorectal cancer: a genome-wide association study to predict toxicity after 5-fluorouracil or FOLFOX administration. Fluorouracil treatment response in colorectal cancer 203 European ancestry cases 791 European ancestry cases Affymetrix [497366] 0 response to 5-fluorouracil http://purl.obolibrary.org/obo/GO_0036275 GCST001403 Genome-wide genotyping array 2012-03-08 22319020 Davies RW 2012-02-07 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/22319020 A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex. Coronary heart disease 7,123 European ancestry cases, 6,826 European ancestry controls 5,211 European ancestry cases, 5,821 European ancestry controls Affymetrix [~ 5000000] (imputed) 5 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001401 Genome-wide genotyping array 2011-07-08 21681796 Fornage M 2011-06-16 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/21681796 Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium. White matter hyperintensity burden 9,361 European ancestry individuals 3,024 European ancestry individuals Affymetrix, Illumina [2153274] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST001109 Genome-wide genotyping array 2010-09-10 20657596 Johansen CT 2010-07-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20657596 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. Hypertriglyceridemia 463 European ancestry cases, 1,197 European ancestry controls NA Affymetrix [~ 2100000] (imputed) 5 Hypertriglyceridemia http://www.ebi.ac.uk/efo/EFO_0004211 GCST000737 Genome-wide genotyping array 2012-03-08 22321639 Pyun JA 2012-02-10 Maturitas www.ncbi.nlm.nih.gov/pubmed/22321639 LAMC1 gene is associated with premature ovarian failure. Premature ovarian failure 24 cases, 24 controls 98 cases, 218 controls Illumina [NR] 0 primary ovarian insufficiency http://www.ebi.ac.uk/efo/EFO_0004266 GCST001406 Genome-wide genotyping array 2013-09-27 23661040 Liao M 2013-05-10 Immunogenetics www.ncbi.nlm.nih.gov/pubmed/23661040 Genome-wide scan on total serum IgE levels identifies no common variants in a healthy Chinese male population. IgE levels 1,999 Han Chinese ancestry males 1,496 East Asian ancestry males Illumina [1940243] (imputed) 0 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST002019 Genome-wide genotyping array 2011-07-08 21679298 Ma X 2011-06-16 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/21679298 A genome-wide association study for quantitative traits in schizophrenia in China. Schizophrenia 98 Chinese ancestry cases, 60 Chinese ancestry controls NA Illumina [464301] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001110 Genome-wide genotyping array 2012-03-13 22341974 Paternoster L 2012-02-16 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22341974 Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position. Facial morphology 2,185 European ancestry adolescent individuals 1,622 European ancestry adolescent individuals Illumina [2543887] (imputed) 1 facial morphology http://www.ebi.ac.uk/efo/EFO_0004743 GCST001412 Genome-wide genotyping array 2011-07-08 21694509 Janicki PK 2011-07-01 Anesthesiology www.ncbi.nlm.nih.gov/pubmed/21694509 Genome-wide Association study using pooled DNA to identify candidate markers mediating susceptibility to postoperative nausea and vomiting. Postoperative nausea and vomiting 122 European ancestry cases, 129 European ancestry controls 104 European ancestry cases, 104 European ancestry controls Illumina [NR] 0 post operative nausea and vomiting http://www.ebi.ac.uk/efo/EFO_0004888 GCST001138 Genome-wide genotyping array 2011-05-27 21533022 Duncan EL 2011-04-21 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21533022 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. Bone mineral density 900 European ancestry female individuals with low hip bone mineral density, 1,055 European ancestry female individuals with high hip bone mineral density 20,898 European ancestry female individuals Illumina [2543887] (imputed) 9 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST001050 Genome-wide genotyping array 2014-04-25 24064335 Pei YF 2013-10-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24064335 Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity. Body mass index 8,463 European ancestry individuals, 7,478 African American individuals, 3,348 Hispanic individuals, 1,624 Han Chinese ancestry individuals 4,979 European ancestry individuals, 2,740 Han Chinese ancestry individuals Affymetrix, Illumina [4325550] (imputed) 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002227 Genome-wide genotyping array 2014-04-25 24064335 Pei YF 2013-10-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24064335 Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity. Fat body mass 6,433 European ancestry individuals, 709 African American individuals, 408 Hispanic individuals, 1,622 Han Chinese ancestry individuals 4,967 European ancestry individuals, 2,740 Han Chinese ancestry individuals Affymetrix, Illumina [4325550] (imputed) 2 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST002226 Genome-wide genotyping array 2011-11-04 21979947 Li X 2011-10-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21979947 A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries. Corneal structure 222 European ancestry cases, 3,324 European ancestry controls 304 European ancestry cases, 518 European ancestry controls, 146 European ancestry cases and 161 European ancestry controls from 70 families Illumina [~ 290000] 5 keratoconus http://purl.obolibrary.org/obo/MONDO_0015486 GCST001261 Genome-wide genotyping array 2010-04-02 20303062 Medland SE 2010-03-18 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20303062 A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure. Digit length ratio 2,889 European ancestry children and adolescents 3,659 European ancestry children Illumina [310613] 1 digit length ratio http://www.ebi.ac.uk/efo/EFO_0004841 GCST000630 Genome-wide genotyping array 2015-04-28 22343285 Bakken TE 2012-02-16 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/22343285 Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans. Occipital cortical area (total cortical area interaction) 421 European ancestry individuals 760 European ancestry individuals Affymetrix [597198] 1 total cortical area measurement, visual cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0008381, http://www.ebi.ac.uk/efo/EFO_0004771 GCST001411 Genome-wide genotyping array 2012-12-05 23010768 Meier S 2012-09-25 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/23010768 Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. Bipolar disorder (Negative mood delusions) 927 European ancestry cases, 2,168 European ancestry controls 1,247 European ancestry cases, 1,434 European ancestry controls Illumina [378570] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001695 Genome-wide genotyping array 2015-05-13 21688384 Wang KS 2011-06-17 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21688384 Genome-wide association analysis of age at onset in schizophrenia in a European-American sample. Schizophrenia (age at onset) 1,162 European ancestry cases 1,068 European ancestry cases Affymetrix [722112] 2 age of onset of schizophrenia http://purl.obolibrary.org/obo/OBA_2001011 GCST001115 Genome-wide genotyping array 2015-05-13 21688384 Wang KS 2011-06-17 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21688384 Genome-wide association analysis of age at onset in schizophrenia in a European-American sample. Schizophrenia (age at onset) (sex interaction) 1,162 European ancestry cases 1,068 European ancestry cases Affymetrix [722112] 0 age of onset of schizophrenia http://purl.obolibrary.org/obo/OBA_2001011 GCST001114 Genome-wide genotyping array 2011-07-08 21682944 Alkelai A 2011-06-20 Int J Neuropsychopharmacol www.ncbi.nlm.nih.gov/pubmed/21682944 DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population. Schizophrenia 155 Jewish-Israeli ancestry cases and 176 Jewish-Israeli ancestry controls from 107 families 99 Arab-Israeli ancestry cases and 99 Arab-Israeli ancestry controls from 57 families Illumina [311517] 2 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001119 Genome-wide genotyping array 2011-10-24 21980348 Fox AA 2011-09-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/21980348 Genome-wide assessment for genetic variants associated with ventricular dysfunction after primary coronary artery bypass graft surgery. Postoperative ventricular dysfunction 76 European ancestry male cases, 1,123 European ancestry controls 188 European ancestry male cases, 1,200 European ancestry male controls Affymetrix [709355] 0 postoperative ventricular dysfunction http://www.ebi.ac.uk/efo/EFO_0004889 GCST001256 Genome-wide genotyping array 2012-03-13 22342860 Marjamaa A 2012-02-15 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/22342860 A common variant near the KCNJ2 gene is associated with T-peak to T-end interval. Early cardiac repolarization 1,870 European ancestry individuals 3,745 European ancestry individuals Illumina [541864] 1 TPE interval measurement http://www.ebi.ac.uk/efo/EFO_0004644 GCST001410 Genome-wide genotyping array 2011-06-01 21540461 Kim DH 2011-05-03 Blood www.ncbi.nlm.nih.gov/pubmed/21540461 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. Chronic myeloid leukemia 201 Korean ancestry cases, 497 Korean ancestry controls 237 Korean ancestry cases, 1,000 Korean ancestry controls, 232 European ancestry cases, 576 European ancestry controls Affymetrix [456522] 2 chronic myelogenous leukemia http://www.ebi.ac.uk/efo/EFO_0000339 GCST001063 Genome-wide genotyping array 2011-06-29 21665993 Han S 2011-06-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21665993 Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore. Corneal curvature 2,008 Chinese ancestry inidividuals, 2,281 Malay ancestry individuals 2,142 Asian Indian ancestry individuals, 929 Chinese ancestry children Illumina [462291] 2 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST001101 Genome-wide genotyping array 2013-05-09 23371916 Dai X 2013-01-31 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/23371916 A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population. Bilirubin levels 1,452 Han Chinese ancestry individuals 8,830 Han Chinese ancestry individuals Affymetrix [658288] (imputed) 10 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST001846 Genome-wide genotyping array 2013-11-15 23746317 Yamaguchi T 2013-05-23 Oral Dis www.ncbi.nlm.nih.gov/pubmed/23746317 Genome-wide association study of degenerative bony changes of the temporomandibular joint. Temporomandibular joint disorder 146 East Asian ancestry cases, 374 East Asian ancestry controls Illumina [532935] 1 temporomandibular joint disorder http://www.ebi.ac.uk/efo/EFO_0005279 GCST002029 Genome-wide genotyping array 2013-08-23 23575436 Go MJ 2013-04-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23575436 New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population. Glycemic traits 7,696 Korean ancestry individuals 6,536 Korean ancestry individuals Affymetrix [357789] 11 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001965 Genome-wide genotyping array 2011-06-03 21573128 Kou I 2011-05-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/21573128 Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese. Osteoporosis 190 Japanese ancestry cases, 1,557 Japanese ancestry controls 2,089 Japanese ancestry cases, 3,114 Japanese ancestry controls Perlegen [224507] 1 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST001071 Genome-wide genotyping array 2011-05-27 21573004 Prescott J 2011-05-10 PLoS One www.ncbi.nlm.nih.gov/pubmed/21573004 Genome-wide association study of relative telomere length. Telomere length 3,554 European ancestry individuals 2,460 European ancestry individuals Illumina [2608509] (imputed) 1 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST001068 Genome-wide genotyping array 2014-03-20 23962720 Speed D 2013-08-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23962720 A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy. Epilepsy (remission after treatment) 889 European and unknown ancestry epilepsy cases NA Illumina [6923995] (imputed) 7 epilepsy, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0000474, http://purl.obolibrary.org/obo/GO_0009410 GCST002141 Genome-wide genotyping array 2012-03-20 22396660 Urabe Y 2012-03-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22396660 A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1. Nephrolithiasis 904 Japanese ancestry cases, 7,471 Japanese ancestry controls 4,892 Japanese ancestry cases, 9,873 Japanese ancestry controls Illumina [556249] 3 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST001432 Genome-wide genotyping array 2011-10-19 21926972 Sklar P 2011-09-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21926972 Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4. Bipolar disorder 7,481 European ancestry cases, 9,250 European ancestry controls 4,496 European ancestry cases, 42,422 European ancestry controls Affymetrix, Illumina [2415422] (imputed) 18 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001241 Genome-wide genotyping array 2012-11-30 22976474 Siddiq A 2012-09-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22976474 A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Breast cancer 3,666 European ancestry cases, 28,864 European ancestry controls, 1,004 African American cases, 2,744 African American controls 562 European ancestry cases, 6,410 European ancestry controls, 84 Japanese ancestry cases, 830 Japanese ancestry controls, 300 Latino cases, 1,164 Latino controls Illumina [2608509] (imputed) 4 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001683 Genome-wide genotyping array 2012-12-06 22969067 Mishra A 2012-09-13 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/22969067 Genetic variants near PDGFRA are associated with corneal curvature in Australians. Corneal curvature 1,788 European ancestry twins and family members, 1,013 European ancestry unrelated individuals NA Illumina [1704858] (imputed) 10 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST001680 Genome-wide genotyping array 2013-07-01 23478653 Han JY 2013-03-12 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/23478653 A genome-wide association study of survival in small-cell lung cancer patients treated with irinotecan plus cisplatin chemotherapy. Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer 139 individuals NA Affymetrix [334127] 7 response to irinotecan http://www.ebi.ac.uk/efo/EFO_0004829 GCST001901 Genome-wide genotyping array 2014-03-04 23966867 Liu CT 2013-08-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23966867 Genome-wide association of body fat distribution in African ancestry populations suggests new loci. Waist circumference Up to 23,564 African American individuals Up to 10,027 African American individuals Affymetrix, Illumina [3200000] (imputed) 7 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST002137 Genome-wide genotyping array 2014-03-04 23966867 Liu CT 2013-08-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23966867 Genome-wide association of body fat distribution in African ancestry populations suggests new loci. Waist-hip ratio up to 19,744 African American individuals Up to 7,606 African American individuals Affymetrix, Illumina [3200000] (imputed) 6 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST002138 Genome-wide genotyping array 2011-05-26 21490707 Cornelis MC 2011-04-07 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21490707 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. Caffeine consumption 47,431 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 10 coffee consumption http://www.ebi.ac.uk/efo/EFO_0004330 GCST001032 Genome-wide genotyping array 2014-04-10 24143190 Low SK 2013-10-15 PLoS One www.ncbi.nlm.nih.gov/pubmed/24143190 Genome-wide association study of breast cancer in the Japanese population. Breast cancer 2,642 Japanese ancestry cases, 2,099 Japanese ancestry controls 2,885 Japanese ancestry cases, 3,395 Japanese ancestry controls Illumina [5335291] (imputed) 4 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST002234 Genome-wide genotyping array 2012-10-12 22907691 Breitfeld J 2012-08-21 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/22907691 Genetic variation in the vaspin gene affects circulating serum vaspin concentrations. Vaspin levels 826 European ancestry individuals 1806 European ancestry individuals Affymetrix [390619] 1 vaspin measurement http://www.ebi.ac.uk/efo/EFO_0004915 GCST001642 Genome-wide genotyping array 2013-11-20 23728934 Yang L 2013-05-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23728934 Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants. Attention deficit hyperactivity disorder 1,040 Han Chinese ancestry cases, 963 Han Chinese ancestry controls NA Affymetrix [656051] 4 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST002048 Genome-wide genotyping array 2011-01-15 21151127 Melum E 2010-12-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21151127 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. Primary sclerosing cholangitis 715 European ancestry cases, 2,962 European ancestry controls 1,025 European ancestry cases, 2,174 European ancestry controls Affymetrix [2466182] (imputed) 2 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST000915 Genome-wide genotyping array 2014-03-15 23979607 Lubke GH 2013-08-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23979607 Genome-wide analyses of borderline personality features. Borderline personality disorder features up to 7,125 individuals 1,301 individuals Affymetrix, Illumina [6670475] 1 borderline personality disorder symptom http://www.ebi.ac.uk/efo/EFO_0005429 GCST002150 Genome-wide genotyping array 2013-04-05 23300701 Jiao S 2012-12-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/23300701 Genome-wide search for gene-gene interactions in colorectal cancer. Colorectal cancer (SNP x SNP interaction) 8,380 European ancestry cases, 10,558 European ancestry controls 2,527 European ancestry cases, 2,628 European ancestry controls Illumina [2011668] 7 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST001794 Genome-wide genotyping array 2013-11-19 20732625 Neale BM 2010-08-01 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/20732625 Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder. Attention deficit hyperactivity disorder 2,064 European ancestry trios, 896 European ancestry cases, 2,455 European ancestry controls NA Affymetrix, Illumina, Perlegen [1206462] (imputed) 5 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST000751 Genome-wide genotyping array 2013-12-10 23738518 Luciano M 2013-06-05 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/23738518 A genome-wide association study for reading and language abilities in two population cohorts. Word reading 6,649 European ancestry children and adolescents Illumina [~ 2400000] (imputed) 15 word reading http://www.ebi.ac.uk/efo/EFO_0005300 GCST002060 Genome-wide genotyping array 2013-12-10 23738518 Luciano M 2013-06-05 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/23738518 A genome-wide association study for reading and language abilities in two population cohorts. Reading and spelling 6,649 European ancestry children and adolescents NA Illumina [~ 2400000] (imputed) 10 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST002062 Genome-wide genotyping array 2013-12-10 23738518 Luciano M 2013-06-05 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/23738518 A genome-wide association study for reading and language abilities in two population cohorts. Non-word repetition 6,649 European ancestry children and adolescents NA Illumina [~ 2400000] (imputed) 5 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST002059 Genome-wide genotyping array 2010-09-01 20622880 Bezzina CR 2010-07-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20622880 Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction. Ventricular fibrillation Up to 515 European ancestry cases, 457 European ancestry controls 146 European ancestry cases, 391 European ancestry controls Illumina [507436] 0 ventricular fibrillation http://www.ebi.ac.uk/efo/EFO_0004287 GCST000725 Genome-wide genotyping array 2015-04-16 21836138 Hadchouel A 2011-08-11 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/21836138 Identification of SPOCK2 as a susceptibility gene for bronchopulmonary dysplasia. Bronchopulmonary dysplasia 22 European ancestry cases, 76 European ancestry controls, 21 African ancestry cases, 86 African ancestry controls 84 European ancestry cases, 267 European ancestry controls, 15 African ancestry cases, 32 African ancestry controls Illumina [up to 660918] 0 bronchopulmonary dysplasia http://purl.obolibrary.org/obo/MONDO_0019091 GCST001197 Genome-wide genotyping array 2015-04-16 21844884 Wheeler HE 2011-08-16 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/21844884 Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations. Response to platinum-based chemotherapy (carboplatin) 176 Sub-Saharan African ancestry lymphoblastoid cell lines, 83 African ancestry lymphoblastoid cell lines, 175 East Asian ancestry lymphoblastoid cell lines, 174 European ancestry lymphoblastoid cell lines NA NR [~ 3000000] (imputed) 18 response to carboplatin http://purl.obolibrary.org/obo/GO_0097328 GCST001204 Genome-wide genotyping array 2015-04-16 21844884 Wheeler HE 2011-08-16 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/21844884 Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations. Response to platinum-based chemotherapy (cisplatin) 176 Sub-Saharan African ancestry lymphoblastoid cell lines, 83 African ancestry lymphoblastoid cell lines, 175 East Asian ancestry lymphoblastoid cell lines, 174 European ancestry lymphoblastoid cell lines NA NR [~ 3000000] (imputed) 21 response to cisplatin http://purl.obolibrary.org/obo/GO_0072718 GCST001201 Genome-wide genotyping array 2011-08-06 21787189 Nyberg F 2011-07-01 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/21787189 Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data. Interstitial lung disease 80 Japanese ancestry cases, 194 Japanese ancestry controls NA Illumina, Perlegen [465816] 2 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST001136 Genome-wide genotyping array 2012-11-06 22951594 Elgazzar S 2012-09-06 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22951594 A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese. Breast cancer 1,086 Japanese ancestry cases, 1,816 Japanese ancestry controls 1,653 Japanese ancestry cases, 2,797 Japanese ancestry controls Illumina [453627] 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001667 Genome-wide genotyping array 2011-04-07 21378986 Wang F 2011-03-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21378986 Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population. Coronary heart disease 230 Han Chinese ancestry cases, 230 Han Chinese ancestry controls 3,240 Han Chinese ancestry cases, 4,353 Han Chinese ancestry controls Illumina [440794] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001000 Genome-wide genotyping array 2015-05-07 22081228 Khor CC 2011-11-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22081228 Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease. Kawasaki disease 405 European ancestry cases, 6,252 European ancestry controls 605 European ancestry cases and 1,349 European ancestry controls from 740 families, 135 cases and 270 controls from 135 families, 1,028 East Asian ancestry cases, 1,512 East Asian ancestry controls Illumina [494236] 2 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST001322 Genome-wide genotyping array 2010-04-02 20305777 Nakajima M 2010-03-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/20305777 New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study. Knee osteoarthritis 899 Japanese ancestry cases, 3,396 Japanese ancestry controls 167 Japanese ancestry cases, 347 Japanese ancestry controls, 813 European ancestry cases, 1,071 European ancestry controls, Illumina [459393] 1 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST000629 Genome-wide genotyping array 2010-08-12 20595679 Feehally J 2010-07-01 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/20595679 HLA has strongest association with IgA nephropathy in genome-wide analysis. Nephropathy 187 European ancestry child cases, 244 European ancestry cases, 4,980 European ancestry controls NA Illumina [286200] 1 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST000718 Genome-wide genotyping array 2013-09-14 23620144 Sulkava S 2013-04-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23620144 Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus. Job-related exhaustion 1,256 European ancestry individuals 13,864 European ancestry individuals Illumina [555388] 1 occupation-related stress disorder http://www.ebi.ac.uk/efo/EFO_0005250 GCST001983 Genome-wide genotyping array 2015-05-08 22076464 Ellinghaus E 2011-11-11 Leukemia www.ncbi.nlm.nih.gov/pubmed/22076464 Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. Acute lymphoblastic leukemia (childhood) 419 European ancestry ETV6-RUNX1 positive cases, 474 European ancestry controls 951 European ancestry ETV6-RUNX1 positive cases, 326 European ancestry ETV6-RUNX1 negative cases, 3,061 European ancestry controls Affymetrix [355750] 31 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST001320 Genome-wide genotyping array 2011-09-03 21771265 Yosifova A 2011-07-19 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/21771265 Genome-wide association study on bipolar disorder in the Bulgarian population. Bipolar disorder 188 Bulgarian ancestry cases, 376 Bulgarian ancestry controls 122 Bulgarian ancestry cases, 328 Bulgarian ancestry controls Illumina [497732] 3 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001164 Genome-wide genotyping array 2011-05-20 21467234 FitzGerald LM 2011-04-05 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/21467234 Genome-wide association study identifies a genetic variant associated with risk for more aggressive prostate cancer. Prostate cancer 202 European ancestry more aggressive cases, 100 European ancestry controls 527 European ancestry more aggressive cases, 595 European ancestry less aggressive cases, 1,167 European ancestry controls Affymetrix [387384] 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001028 Genome-wide genotyping array 2011-11-24 22037553 Haiman CA 2011-10-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22037553 A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer. Breast cancer 1,004 African American cases, 2,745 African American controls,1,718 European ancestry cases, 3,670 European ancestry controls 2,292 European ancestry cases, 16,901 European ancestry controls Illumina [3154485] (imputed) 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001298 Genome-wide genotyping array 2011-11-24 22020760 Won HH 2011-10-21 Cancer www.ncbi.nlm.nih.gov/pubmed/22020760 Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients. Response to platinum-based agents 96 colon cancer cases 247 colon cancer cases Affymetrix [656843] 3 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST001291 Genome-wide genotyping array 2014-01-08 23793025 Anttila V 2013-06-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23793025 Genome-wide meta-analysis identifies new susceptibility loci for migraine. Migraine without aura 7,107 European ancestry cases, 69,427 European ancestry controls NA Affymetrix, Illumina [~ 2300000] (imputed) 32 migraine without aura, susceptibility to, 4 http://purl.obolibrary.org/obo/MONDO_0011847 GCST002078 Genome-wide genotyping array 2014-01-08 23793025 Anttila V 2013-06-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23793025 Genome-wide meta-analysis identifies new susceptibility loci for migraine. Migraine with aura 5,118 European ancestry cases, 74,239 European ancestry controls NA Affymetrix, Illumina [~ 2300000] (imputed) 23 migraine with aura http://purl.obolibrary.org/obo/MONDO_0005475 GCST002080 Genome-wide genotyping array 2014-01-08 23793025 Anttila V 2013-06-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23793025 Genome-wide meta-analysis identifies new susceptibility loci for migraine. Migraine 23,285 European ancestry cases, 95,425 European ancestry controls NA Affymetrix, Illumina [~ 2300000] (imputed) 59 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST002081 Genome-wide genotyping array 2014-01-08 23793025 Anttila V 2013-06-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23793025 Genome-wide meta-analysis identifies new susceptibility loci for migraine. Migraine - clinic-based 5,175 European ancestry clinic-based cases, 13,972 European ancestry clinic-based controls NA Affymetrix, Illumina [~ 2300000] (imputed) 37 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST002079 Genome-wide genotyping array 2013-04-12 23326512 Greenwood TA 2013-01-10 PLoS One www.ncbi.nlm.nih.gov/pubmed/23326512 Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder. Bipolar disorder (mania) 117 European ancestry Irritable mania cases, 843 European ancestry Elated mania cases, 1033 European ancestry controls 121 European ancestry Irritable maniacases, 1026 European ancestry Elated mania cases Affymetrix [703012] 1 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001811 Genome-wide genotyping array 2010-04-02 20228799 McGovern DP 2010-03-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20228799 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. Ulcerative colitis 2,693 European ancestry cases, 6,791 European ancestry controls 2,009 European ancestry cases, 1,580 European ancestry controls Illumina [266047] 21 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST000624 Genome-wide genotyping array 2010-03-26 20231535 Smith NL 2010-03-15 Circulation www.ncbi.nlm.nih.gov/pubmed/20231535 Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Factor VIII levels 15,279 European ancestry individuals up to 7,604 European ancestry individuals Affymetrix, Illumina [2729294] (imputed) 2 factor VIII measurement http://www.ebi.ac.uk/efo/EFO_0004630 GCST000626 Genome-wide genotyping array 2016-04-01 20231535 Smith NL 2010-03-15 Circulation www.ncbi.nlm.nih.gov/pubmed/20231535 Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. Factor VII levels 15,422 European ancestry individuals Up to 7,604 European ancestry individuals Affymetrix, Illumina [2734954] (imputed) 2 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST000625 Genome-wide genotyping array 2016-04-01 20231535 Smith NL 2010-03-15 Circulation www.ncbi.nlm.nih.gov/pubmed/20231535 Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium. vWF levels 17,596 European ancestry individuals Up to 7,604 European ancestry individuals Affymetrix, Illumina [2742821] (imputed) 4 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST000627 Genome-wide genotyping array 2010-03-15 20173747 Ellinor PT 2010-02-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20173747 Common variants in KCNN3 are associated with lone atrial fibrillation. Atrial fibrillation 1,335 European ancestry cases, 12,844 European ancestry controls 1,164 European ancestry cases, 3,607 European ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 3 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST000602 Genome-wide genotyping array 2012-03-23 22344221 Okada Y 2012-02-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22344221 Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations. Body mass index (SNP x SNP interaction) 26,620 Japanese ancestry individuals 35,625 East Asian ancestry individuals Illumina [2178018] (imputed) 10 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST001416 Genome-wide genotyping array 2020-01-09 23823483 Rhee EP 2013-07-02 Cell Metab www.ncbi.nlm.nih.gov/pubmed/23823483 A genome-wide association study of the human metabolome in a community-based cohort. Metabolite levels 2,076 European ancestry individuals NA Affymetrix [at least 2500000] (imputed) 2148 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST009391 Genome-wide genotyping array 2011-06-29 21666691 Sun LD 2011-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21666691 Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population. Atopic dermatitis 1,012 Han Chinese ancestry cases, 1,362 Han Chinese ancestry controls 3,624 Han Chinese ancestry cases, 12,197 Han Chinese ancestry controls, 1,806 European ancestry cases, 3,256 European ancestry controls Illumina [491905] 1 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST001106 Genome-wide genotyping array 2012-11-28 22968431 Urban TJ 2012-09-09 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/22968431 Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs. Drug-induced liver injury 783 European ancestry cases, 3,001 European ancestry controls 307 European ancestry cases, 2,587 European ancestry controls Illumina [800769] 1 drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0004228 GCST001673 Genome-wide genotyping array 2010-05-26 20436469 Beaty TH 2010-05-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20436469 A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Cleft lip 825 European ancestry trios, 1,038 Asian ancestry trios 2,194 Asian ancestry family members, 322 South Asian ancestry family members, 3,830 European ancestry family members, 1,769 South and Central American ancestry family members Illumina [589945] 2 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST000673 Genome-wide genotyping array 2012-06-18 22494929 Rawal R 2012-04-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22494929 Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function. Thyroid function 3,736 European ancestry individuals 3,727 European ancestry individuals Affymetrix, Illumina [2524918] (imputed) 4 thyroid function http://www.ebi.ac.uk/efo/EFO_0004296 GCST001487 Genome-wide genotyping array 2011-07-29 21755009 Wheeler HE 2011-07-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/21755009 Genome-wide local ancestry approach identifies genes and variants associated with chemotherapeutic susceptibility in African Americans. Chemotherapeutic susceptibility 83 African American lymphoblastoid cell lines, 176 African ancestry lymphoblastoid cell lines NA NR [2217232] (imputed) 0 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST001145 Genome-wide genotyping array 2012-11-28 22986903 Hansel NN 2012-09-18 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22986903 Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD. Chronic obstructive pulmonary disease 4,048 European ancestry cases 1,772 European ancestry cases, 4,733 cases Illumina [528817] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST001686 Genome-wide genotyping array 2010-05-07 20386566 Lee MT 2010-04-13 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20386566 Genome-wide association study of bipolar I disorder in the Han Chinese population. Bipolar I disorder 1,000 Han Chinese ancestry cases, 1,000 Han Chinese ancestry controls 409 Han Chinese ancestry cases, 1,000 Han Chinese ancestry controls Illumina [516919] 2 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST000654 Genome-wide genotyping array 2010-05-03 20360315 Uher R 2010-04-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/20360315 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. Response to antidepressants 706 European ancestry individuals NA Illumina [539391] 8 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST000643 Genome-wide genotyping array 2012-11-04 22951725 Tang XF 2012-09-06 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/22951725 Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population. Vitiligo 1,117 Han Chinese ancestry cases, 1,701 Han Chinese ancestry controls 5,740 Han Chinese ancestry cases, 10,324 Han Chinese ancestry controls Illumina [493909] 4 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST001670 Genome-wide genotyping array 2012-03-15 22362865 Knaapila A 2012-02-23 Chem Senses www.ncbi.nlm.nih.gov/pubmed/22362865 A genome-wide study on the perception of the odorants androstenone and galaxolide. Odorant perception 1,573 European ancestry young-adult twins and singleton siblings 200 European ancestry adult monozygous twin individuals, 26 European ancestry adult dizygous twin individuals Illumina [2300000] (imputed) 0 sensory perception of smell http://purl.obolibrary.org/obo/GO_0007608 GCST001422 Genome-wide genotyping array 2014-10-06 24529757 Xie T 2014-01-17 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/24529757 Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations. Amyotrophic lateral sclerosis (sporadic) 250 Han Chinese ancestry cases, 250 Han Chinese ancestry controls NA Illumina [859311] 175 sporadic amyotrophic lateral sclerosis http://www.ebi.ac.uk/efo/EFO_0001357 GCST002337 Genome-wide genotyping array 2011-08-12 21757650 Debette S 2011-07-14 Circ Res www.ncbi.nlm.nih.gov/pubmed/21757650 Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels. Vascular endothelial growth factor levels 3,527 European ancestry individuals 1,727 European ancestry individuals Affymetrix [2540233] (imputed) 4 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST001155 Genome-wide genotyping array 2014-11-07 24743840 Figueiredo JC 2014-04-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24743840 Genome-wide diet-gene interaction analyses for risk of colorectal cancer. Colorectal cancer (diet interaction) 9,287 European ancestry cases, 9,117 European ancestry controls NA Affymetrix, Illumina [> 2700000] (imputed) 13 diet measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0008111, http://purl.obolibrary.org/obo/MONDO_0005575 GCST002415 Genome-wide genotyping array 2012-09-26 22841784 Patin E 2012-07-26 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/22841784 Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection. Hepatitis C induced liver fibrosis 1,161 European ancestry HCV-infected individuals 1,181 European ancestry HCV-infected individuals Illumina [780650] (imputed) 6 hepatitis C virus infection, cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0003047, http://www.ebi.ac.uk/efo/EFO_0001422 GCST001623 Genome-wide genotyping array 2012-09-25 22829776 Coviello AD 2012-07-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22829776 A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation. Sex hormone-binding globulin levels 21,791 European ancestry individuals 8,175 European ancestry individuals Affymetrix, Illumina [2543887] (imputed) 30 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST001612 Genome-wide genotyping array 2013-01-23 23143602 Whitcomb DC 2012-11-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23143602 Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Pancreatitis 676 European ancestry cases, 4,507 European ancestry controls 910 European ancestry cases, 4,170 European ancestry controls Illumina [625739] 5 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST001741 Genome-wide genotyping array 2012-11-28 22990020 Huang J 2012-09-18 Blood www.ncbi.nlm.nih.gov/pubmed/22990020 Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Plasminogen activator inhibitor type 1 levels (PAI-1) 19,599 European ancestry individuals 10,764 European ancestry individuals Affymetrix, Illumina [2445683] (imputed) 4 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST001684 Genome-wide genotyping array 2010-03-30 20208534 Rothenberg ME 2010-03-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20208534 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. Eosinophilic esophagitis (pediatric) 181 European ancestry cases, 1,974 European ancestry controls 170 European ancestry cases, 1,130 European ancestry controls Illumina [~ 550000] 14 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST000620 Genome-wide genotyping array 2013-01-09 23053960 Lee YH 2012-10-07 Mol Biol Rep www.ncbi.nlm.nih.gov/pubmed/23053960 Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis. Systemic lupus erythematosus 1,527 European ancestry cases, 3,421 European ancestry controls, NA Illumina [737984] 5 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST001708 Genome-wide genotyping array 2011-05-27 21551455 Kanetsky PA 2011-05-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/21551455 A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility. Testicular cancer 349 European ancestry cases, 919 European ancestry controls 439 European ancestry cases, 960 European ancestry controls Affymetrix [609482] 2 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST001067 Genome-wide genotyping array 2012-11-13 22935194 Connolly JJ 2012-08-30 Child Dev www.ncbi.nlm.nih.gov/pubmed/22935194 A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scale. Autism Up to 2,165 European, African American, East Asian and South Asian ancestry individuals Up to 1,231 individuals Illumina [522149] 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST001655 Genome-wide genotyping array 2011-08-04 21752600 Chen J 2011-07-12 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/21752600 Two non-synonymous markers in PTPN21, identified by genome-wide association study data-mining and replication, are associated with schizophrenia. Schizophrenia 1,658 European ancestry cases, 1,655 European ancestry controls 5,995 European ancestry cases, 5,902 European ancestry controls, 455 European ancestry individuals, 1,142 African American cases, 985 African American controls Affymetrix, Perlegen [up to 727905] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001151 Genome-wide genotyping array 2011-10-17 21926974 Ripke S 2011-09-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21926974 Genome-wide association study identifies five new schizophrenia loci. Schizophrenia 9,394 European ancestry cases, 12,462 European ancestry controls 8,442 European ancestry cases, 21,397 European ancestry controls Affymetrix, Illumina [1252901] (imputed) 25 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001242 Genome-wide genotyping array 2013-02-06 23184150 Henrion M 2012-11-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23184150 Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer. Renal cell carcinoma 2,215 European ancestry cases, 8,566 European ancestry controls 3,739 European ancestry cases, 8,786 European ancestry controls Illumina [284377] 2 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST001750 Genome-wide genotyping array 2011-06-01 21532571 Burdon KP 2011-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21532571 Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. Glaucoma 590 European ancestry cases, 3,956 European ancestry controls 892 European ancestry advanced cases, 4,582 European ancestry less severe cases Illumina [298778] 2 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST001062 Genome-wide genotyping array 2013-08-21 23263444 Frazier-Wood AC 2012-12-22 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23263444 Genetic variants associated with VLDL, LDL and HDL particle size differ with race/ethnicity. Lipoprotein diameter 817 European ancestry individuals 2,430 European ancestry individuals, 1,594 African American individuals, 1,422 Hispanic individuals, 758 Chinese ancestry individuals Affymetrix [2543887] (imputed) 0 bronchopulmonary dysplasia http://purl.obolibrary.org/obo/MONDO_0019091 GCST001789 Genome-wide genotyping array 2013-06-28 23446634 Chen Z 2013-02-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23446634 Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network. Red blood cell traits Up to 16,485 African American individuals 9,692 African American individuals, 21,020 European ancestry individuals, 14,088 Japanese ancestry individuals Affymetrix, Illumina [NR] 15 hemoglobin measurement, erythrocyte count, mean corpuscular hemoglobin concentration, mean corpuscular volume, hematocrit, obsolete_red blood cell distribution width, mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0004305, http://www.ebi.ac.uk/efo/EFO_0004528, http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004348, http://www.ebi.ac.uk/efo/EFO_0005192, http://www.ebi.ac.uk/efo/EFO_0004527 GCST001873 Genome-wide genotyping array 2013-02-01 23143601 Lan Q 2012-11-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23143601 Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia. Lung cancer 5,510 East Asian ancestry cases, 4,544 East Asian ancestry controls 1,099 East Asian ancestry cases, 2,913 East Asian ancestry controls Illumina [596032] 7 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST001740 Genome-wide genotyping array 2014-04-08 24216480 Song YQ 2013-10-08 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/24216480 Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant. Disc degeneration (lumbar) 366 Japanese ancestry cases, 3,331 Japanese ancestry controls 1,628 East Asian ancestry cases, 17,469 East Asian ancestry controls, 399 European ancestry cases, 5,035 European ancestry control Illumina [464775] 2 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST002225 Genome-wide genotyping array 2011-08-02 21668797 Agrawal A 2010-11-04 Addict Biol www.ncbi.nlm.nih.gov/pubmed/21668797 A genome-wide association study of DSM-IV cannabis dependence. Cannabis dependence 708 African American or European ancestry cases, 2,346 African American or European ancestry controls NA Illumina [948142] 10 cannabis dependence http://www.ebi.ac.uk/efo/EFO_0007191 GCST000861 Genome-wide genotyping array 2014-03-25 24058526 Bhatnagar P 2013-09-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/24058526 Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease. Systolic blood pressure in sickle cell anemia 1617 African American cases NA Illumina [1019297] (imputed) 10 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST002187 Genome-wide genotyping array 2014-03-11 23956247 Knevel R 2013-08-16 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/23956247 Identification of a genetic variant for joint damage progression in autoantibody-positive rheumatoid arthritis. Joint damage progression in ACPA-positive rheumatoid arthritis 384 cases 301 European ancestry cases, 742 cases Illumina [391733] 0 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST002139 Genome-wide genotyping array 2013-08-21 21738480 Nalls MA 2011-07-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21738480 Multiple loci are associated with white blood cell phenotypes. White blood cell count 19,509 European ancestry individuals 11,823 European ancestry individuals Affymetrix, Illumina [> 2400000] (imputed) 10 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST001137 Genome-wide genotyping array 2014-10-28 24554482 Leger PD 2014-02-20 J Neurovirol www.ncbi.nlm.nih.gov/pubmed/24554482 Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384. Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 1 peripheral neuropathy) 40 European ancestry cases, 37 African American cases, 13 Hispanic cases, 85 European ancestry controls, 49 African American controls, 30 Hispanic controls NA Illumina [936149] 11 response to reverse transcriptase inhibitor http://purl.obolibrary.org/obo/GO_0061479 GCST002366 Genome-wide genotyping array 2014-10-28 24554482 Leger PD 2014-02-20 J Neurovirol www.ncbi.nlm.nih.gov/pubmed/24554482 Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384. Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 3 peripheral neuropathy) 8 European ancestry cases, 12 African American cases, 3 Hispanic cases, 85 European ancestry controls, 49 African American controls, 30 Hispanic controls NA Illumina [936149] 16 response to reverse transcriptase inhibitor http://purl.obolibrary.org/obo/GO_0061479 GCST002363 Genome-wide genotyping array 2014-10-28 24554482 Leger PD 2014-02-20 J Neurovirol www.ncbi.nlm.nih.gov/pubmed/24554482 Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384. Response to anti-retroviral therapy (ddI/d4T) in HIV-1 infection (Grade 2 peripheral neuropathy) 19 European ancestry cases, 30 African American cases, 9 Hispanic cases, 85 European ancestry controls, 49 African American controls, 30 Hispanic controls NA Illumina [936149] 13 response to reverse transcriptase inhibitor http://purl.obolibrary.org/obo/GO_0061479 GCST002365 Genome-wide genotyping array 2014-10-03 24448986 Zhang B 2014-01-21 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/24448986 Genome-wide association study identifies a new SMAD7 risk variant associated with colorectal cancer risk in East Asians. Colorectal cancer 1,773 East Asian ancestry cases, 2,642 East Asian ancestry controls 6,902 East Asian ancestry cases, 7,862 East Asian ancestry controls Affymetrix, Illumina [1695815] (imputed) 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002340 Genome-wide genotyping array 2014-03-23 24045676 Pyun JA 2013-09-16 Menopause www.ncbi.nlm.nih.gov/pubmed/24045676 Genome-wide association studies and epistasis analyses of candidate genes related to age at menarche and age at natural menopause in a Korean population. Menopause (age at onset) 1,827 Korean ancestry females NA Affymetrix [343107] 2 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST002192 Genome-wide genotyping array 2014-03-23 24045676 Pyun JA 2013-09-16 Menopause www.ncbi.nlm.nih.gov/pubmed/24045676 Genome-wide association studies and epistasis analyses of candidate genes related to age at menarche and age at natural menopause in a Korean population. Menarche (age at onset) 3,437 Korean ancestry females NA Affymetrix [343637] 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST002191 Genome-wide genotyping array 2011-06-03 21573907 Parra EJ 2011-05-15 Diabetologia www.ncbi.nlm.nih.gov/pubmed/21573907 Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas. Type 2 diabetes 1,804 Hispanic cases, 780 Hispanic controls European ancestry individuals Affymetrix [315658] 5 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001070 Genome-wide genotyping array 2013-06-06 23419831 Ramanan VK 2013-02-19 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23419831 APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study. Alzheimer's disease biomarkers 555 European ancestry individuals NA Illumina [6108668] (imputed) 13 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001868 Genome-wide genotyping array 2011-11-15 21998597 Ohlsson C 2011-10-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21998597 Genetic determinants of serum testosterone concentrations in men. Testosterone levels 8,938 European ancestry male individuals 5,491 European ancestry male individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST001264 Genome-wide genotyping array 2014-11-06 24952865 Akerblom A 2014-04-04 Am Heart J www.ncbi.nlm.nih.gov/pubmed/24952865 Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study. Plasma cystastin c levels in acute coronary syndrome 9,801 European ancestry cases, 57 Black cases, 90 Oriental ancestry cases, 30 cases NA Illumina [619657] 2 acute coronary syndrome http://www.ebi.ac.uk/efo/EFO_0005672 GCST002406 Genome-wide genotyping array 2014-04-04 24049095 Chen Z 2013-09-18 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24049095 Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men. Follicle stimulating hormone levels 1,999 Han Chinese ancestry individuals 1,496 East Asian ancestry individuals Illumina [709211] 6 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST002199 Genome-wide genotyping array 2014-04-04 24049095 Chen Z 2013-09-18 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24049095 Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men. Hormone measurements 1,999 Han Chinese ancestry individuals 1,496 East Asian ancestry individuals Illumina [709211] 7 estradiol measurement, sex hormone-binding globulin measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004697, http://www.ebi.ac.uk/efo/EFO_0004696, http://www.ebi.ac.uk/efo/EFO_0004908 GCST002195 Genome-wide genotyping array 2015-04-23 24983941 Tang W 2014-07-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/24983941 Large-scale genome-wide association studies and meta-analyses of longitudinal change in adult lung function. Rate of change of FEV1 (time interaction) up to 27,249 European ancestry individuals 1,494 individuals, 4,084 mild chronic obstructive pulmonary disease smoker individuals Affymetrix, Illumina [up to 2470255] 0 FEV change measurement, forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0005921, http://www.ebi.ac.uk/efo/EFO_0004314 GCST002517 Genome-wide genotyping array 2010-07-30 20558539 Kestenbaum B 2010-06-17 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/20558539 Common genetic variants associate with serum phosphorus concentration. Phosphorus levels 16,264 European ancestry individuals 5,444 individuals Affymetrix, Illumina [~ 2500000] (imputed) 5 phosphorus measurement http://www.ebi.ac.uk/efo/EFO_0004861 GCST000703 Genome-wide genotyping array 2008-09-30 18347602 Sullivan PF 2008-03-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/18347602 Genomewide association for schizophrenia in the CATIE study: results of stage 1. Schizophrenia 417 European ancestry cases, 411 European ancestry controls, 217 African American cases, 219 African American controls, 104 American Indian, Asian, Pacific Islander or Hispanic/Latino ancestry cases, 103 American Indian, Asian, Pacific Islander or Hispanic/Latino ancestry controls NA Affymetrix [492900] 6 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000164 Genome-wide genotyping array 2014-10-09 24465473 Liu Y 2014-01-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/24465473 A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese. Telomere length 2,632 Han Chinese ancestry individuals 3,917 Han Chinese ancestry individuals, 696 European ancestry individuals Affymetrix [585206] 2 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST002341 Genome-wide genotyping array 2011-06-01 21546496 Guerrero JA 2011-05-03 Haematologica www.ncbi.nlm.nih.gov/pubmed/21546496 Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children. Platelet function and related traits 70 children 286 children Illumina [320610] 1 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST001065 Genome-wide genotyping array 2008-06-16 18372901 Tenesa A 2008-03-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18372901 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. Colorectal cancer 981 European ancestry cases, 1,002 European ancestry controls 10,287 European ancestry cases, 10,401 European ancestry controls, 4,400 Japanese ancestry cases, 3,179 Japanese ancestry controls, 1,789 cases, 1,771 controls Illumina [541628] 3 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000168 Genome-wide genotyping array 2014-02-11 23886662 Weidinger S 2013-07-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23886662 A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis. Atopic dermatitis 1563 European ancestry cases, 4,054 European ancestry controls 2,286 European ancestry cases, 3,160 European ancestry controls Illumina [2406139] (imputed) 4 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST002100 Genome-wide genotyping array 2009-01-15 19056611 Timpson NJ 2008-12-03 Diabetes www.ncbi.nlm.nih.gov/pubmed/19056611 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. Type 2 diabetes 958 European ancestry obese cases, 955 European ancestry non-obese cases, 2,938 European ancestry controls Up to 3,757 European ancestry cases, up to 5,346 European ancestry controls Affymetrix [393453] 8 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000277 Genome-wide genotyping array 2009-12-28 19966805 Wallace C 2009-12-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19966805 The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes. Type 1 diabetes 7,514 European ancestry cases, 9,045 European ancestry controls 4,840 European ancestry cases, 2,670 European ancestry controls, 5,766 European ancestry familial triads Affymetrix, Illumina [~ 2600000] (imputed) 2 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST000539 Genome-wide genotyping array 2014-11-26 24958192 Gusareva ES 2014-05-28 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/24958192 Genome-wide association interaction analysis for Alzheimer's disease. Alzheimer's disease (SNP x SNP interaction) 2,259 European ancestry cases, 6,017 European ancestry controls 2,585 European ancestry cases, 4,491 European ancestry controls, 4,039 cases, 6,736 controls Illumina [312480] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002462 Genome-wide genotyping array 2009-02-26 19060907 Prokopenko I 2008-12-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060907 Variants in MTNR1B influence fasting glucose levels. Fasting plasma glucose 35,812 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 2557249] (imputed) 3 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000276 Genome-wide genotyping array 2008-11-12 18978787 Wang Y 2008-11-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18978787 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. Lung cancer 5,095 European ancestry cases, 5,200 European ancestry controls 2,448 European ancestry cases, 2,983 European ancestry controls Illumina [223891] 3 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST000257 Genome-wide genotyping array 2014-12-11 24919509 Terao C 2014-06-11 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24919509 A genome-wide association study of serum levels of prostate-specific antigen in the Japanese population. Prostate-specific antigen levels 1,086 Japanese ancestry males 1,302 Japanese ancestry males Illumina [303283] 2 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST002476 Genome-wide genotyping array 2010-05-25 20421499 Levy D 2010-04-26 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/20421499 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. Telomere length 3,417 European ancestry individuals 1,893 African American and European ancestry individuals, 2,876 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 4 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST000669 Genome-wide genotyping array 2010-06-14 20484958 Diergaarde B 2010-05-17 Pancreatology www.ncbi.nlm.nih.gov/pubmed/20484958 Pooling-based genome-wide association study implicates gamma-glutamyltransferase 1 (GGT1) gene in pancreatic carcinogenesis. Pancreatic cancer 97 European ancestry cases, 93 European ancestry controls 63 European ancestry cases, 79 European ancestry controls Affymetrix [> 900000] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST000686 Genome-wide genotyping array 2015-09-15 25387706 Vaidyanathan U 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387706 Heritability and molecular genetic basis of electrodermal activity: a genome-wide association study. Electrodermal activity Up to 4,424 European ancestry twins and their parents NA Illumina [527829] 13 skin conductance level, skin conductance response frequency, electrodermal activity measurement, skin conductance response amplitude http://www.ebi.ac.uk/efo/EFO_0006867, http://www.ebi.ac.uk/efo/EFO_0006869, http://www.ebi.ac.uk/efo/EFO_0006866, http://www.ebi.ac.uk/efo/EFO_0006868 GCST002706 Genome-wide genotyping array 2015-06-12 25457201 de Tayrac M 2014-10-18 J Hepatol www.ncbi.nlm.nih.gov/pubmed/25457201 Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis. Hereditary hemochromatosis-related traits (HFE mutation homozygotes) 474 European ancestry cases 746 European ancestry cases Illumina [534213] 2 hereditary hemochromatosis type 1, transferrin measurement, serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006513, http://www.ebi.ac.uk/efo/EFO_0006341, http://www.ebi.ac.uk/efo/EFO_0006332 GCST002660 Genome-wide genotyping array 2014-05-28 24256812 Fogh I 2013-11-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24256812 A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis (sporadic) 6,100 European ancestry cases, 7,125 European ancestry controls 2,074 European ancestry cases, 2,556 European ancestry controls Illumina [~ 7000000] (imputed) 4 sporadic amyotrophic lateral sclerosis http://www.ebi.ac.uk/efo/EFO_0001357 GCST002283 Genome-wide genotyping array 2015-05-16 25451450 Jacobsen KK 2014-10-12 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/25451450 Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder. Migraine in bipolar disorder 460 European ancestry cases with migraine, 914 European ancestry cases without migraine 289 European ancestry cases with migraine, 697 European ancestry without migraine Affymetrix [723224] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST002656 Genome-wide genotyping array 2014-12-10 24751813 Drago A 2014-06-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/24751813 Genome-wide association study supports the role of the immunological system and of the neurodevelopmental processes in response to haloperidol treatment. Response to haloperidol in psychosis 96 European ancestry cases NA Illumina [1080870] (imputed) 2 response to haloperidol http://purl.obolibrary.org/obo/GO_1905119 GCST002465 Genome-wide genotyping array 2015-10-24 25569183 Vijai J 2015-01-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25569183 A genome-wide association study of marginal zone lymphoma shows association to the HLA region. Marginal zone lymphoma 825 European ancestry cases, 6,221 European ancestry controls 456 European ancestry cases, 906 European ancestry controls Illumina [611856] 4 marginal zone B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_1000630 GCST002742 Genome-wide genotyping array 2014-10-10 24449572 Orozco G 2014-01-01 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/24449572 Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study. Rheumatoid arthritis 3,034 European ancestry cases, 5,271 European ancestry controls 4,726 European ancestry cases, 2,625 European ancestry controls Affymetrix, Illumina [1831729] (imputed) 8 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST002323 Genome-wide genotyping array 2014-10-28 24586186 Rueedi R 2014-02-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24586186 Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links. Urinary metabolites (H-NMR features) 835 European ancestry individuals 601 Brazilian individuals Illumina [713870] (imputed) 39 urinary metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005116 GCST002364 Genome-wide genotyping array 2010-05-31 20436471 Albagha OM 2010-05-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20436471 Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone. Paget's disease 692 European ancestry cases, 1,001 European ancestry controls 256 European ancestry cases, 488 European ancestry controls Illumina [294663] 4 osteitis deformans http://www.ebi.ac.uk/efo/EFO_0004261 GCST000672 Genome-wide genotyping array 2014-10-01 24430505 Moayyeri A 2014-01-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24430505 Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Bone properties (heel) 730 East Asian ancestry individuals, 2,380 European ancestry individuals, 11,150 individuals 11,058 European ancestry individuals, 2,870 European and other ancestry individuals, 21,439 individuals Affymetrix, Illumina [up to 2609590] (imputed) 8 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST002335 Genome-wide genotyping array 2014-10-01 24430505 Moayyeri A 2014-01-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24430505 Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Bone properties (heel) 4,556 European ancestry individuals 2,236 European ancestry individuals Affymetrix, Illumina [up to 2399195] (imputed) 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST002334 Genome-wide genotyping array 2014-10-01 24430505 Moayyeri A 2014-01-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24430505 Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium. Bone properties (heel) 2,483 East Asian ancestry individuals, 1,885 European ancestry individuals, 11,146 individuals 10,074 European ancestry individuals, 2,870 European and other ancestry individuals, 21,434 individuals Affymetrix, Illumina [up to 2609590] (imputed) 10 velocity of sound measurement http://www.ebi.ac.uk/efo/EFO_0005654 GCST002333 Genome-wide genotyping array 2015-05-07 25217961 Al Olama AA 2014-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25217961 A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer. Prostate cancer 34,379 European ancestry cases, 33,164 European ancestry controls, 5,327 African ancestry cases, 5,136 African ancestry controls, 2,563 Japanese ancestry cases, 4,391 Japanese ancestry controls, 1,034 Latino cases, 1,046 Latino controls NA Affymetrix, Illumina [up to 16852405] (imputed) 41 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002606 Genome-wide genotyping array 2014-10-30 24578125 Olden M 2014-02-27 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/24578125 Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis. Urinary uromodulin levels 10,884 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 5 urinary uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0005663 GCST002376 Genome-wide genotyping array 2015-07-15 25429064 He M 2014-11-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25429064 Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. Height 36,227 East Asian ancestry individuals 57,699 East Asian ancestry individuals Affymetrix, Illumina [2704730] (imputed) 125 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST002702 Genome-wide genotyping array 2015-04-28 23092984 Goes FS 2012-10-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/23092984 Genome-wide association of mood-incongruent psychotic bipolar disorder. Bipolar disorder with mood-incongruent psychosis 2,196 European and other ancestry cases, 8,148 European and other ancestry controls NA Affymetrix, Illumina [~ 2500000] (imputed) 16 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST001715 Genome-wide genotyping array 2015-05-29 25223902 Go MJ 2014-09-16 Genomics www.ncbi.nlm.nih.gov/pubmed/25223902 A genome-wide association study identifies a LEPR gene as a novel predisposing factor for childhood fasting plasma glucose. Fasting plasma glucose (childhood) 484 Korean ancestry children 776 Korean ancestry children Illumina [747076] 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST002610 Genome-wide genotyping array 2014-02-12 23834954 Kobayashi D 2013-07-08 Mol Pain www.ncbi.nlm.nih.gov/pubmed/23834954 Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy. Sensory disturbances after bilateral sagittal split ramus osteotomy Up to 105 individuals Up to 200 individuals Illumina [243229] 7 post-operative sensory disturbance http://www.ebi.ac.uk/efo/EFO_0005324 GCST002090 Genome-wide genotyping array 2015-06-24 25456346 Nievergelt CM 2014-10-30 Psychoneuroendocrinology www.ncbi.nlm.nih.gov/pubmed/25456346 Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene. Post-traumatic stress disorder 940 European, Hispanic, Native American, African American, East Asian and other ancestry cases, 2,554 European, Hispanic, Native American, African American, East Asian and other ancestry trauma-exposed controls 313 European ancestry cases, 178 European ancestry trauma-exposed controls Illumina [21693469] (imputed) 7 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST002681 Genome-wide genotyping array 2015-07-24 25476525 Germain M 2014-12-06 Diabetologia www.ncbi.nlm.nih.gov/pubmed/25476525 SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes. Diabetic nephropathy in type 1 diabetes 683 European ancestry cases, 779 European ancestry controls 2,962 European ancestry cases, 3,379 European ancestry controls Illumina [11133962] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST002716 Genome-wide genotyping array 2015-06-30 25096692 Chung WH 2014-08-06 JAMA www.ncbi.nlm.nih.gov/pubmed/25096692 Genetic variants associated with phenytoin-related severe cutaneous adverse reactions. Phenytoin-induced severe cutaneous adverse reactions 60 Han Chinese ancestry cases, 412 Han Chinese ancestry controls 39 East Asian ancestry cases, 130 Han Chinese ancestry phenytoin-tolerant controls, 2,869 Japanese ancestry controls, 6 Asian ancestry cases, 374 Asian ancestry controls Affymetrix [854035] 0 severe cutaneous adverse reaction, response to phenytoin http://www.ebi.ac.uk/efo/EFO_0006346, http://www.ebi.ac.uk/efo/EFO_0006345 GCST002558 Genome-wide genotyping array 2015-07-27 25429627 Oryoji D 2014-11-27 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/25429627 Identification of a Hashimoto thyroiditis susceptibility locus via a genome-wide comparison with Graves' disease. Hashimoto thyroiditis versus Graves' disease 263 Japanese ancestry Hashimoto thyroiditis cases, 260 Japanese ancestry Graves’ disease cases 181 Japanese ancestry Hashimoto thyroiditis cases, 286 Japanese ancestry Graves’ disease cases Illumina [546173] 3 autoimmune thyroid disease, Hashimoto's thyroiditis, Graves disease http://www.ebi.ac.uk/efo/EFO_0006812, http://www.ebi.ac.uk/efo/EFO_0003779, http://www.ebi.ac.uk/efo/EFO_0004237 GCST002705 Genome-wide genotyping array 2015-10-26 25574032 Lee H 2015-01-08 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/25574032 Genome-wide association study identified new susceptibility loci for polycystic ovary syndrome. Polycystic ovary syndrome 976 Korean ancestry cases, 946 Korean ancestry controls 249 Korean ancestry cases, 778 Korean ancestry controls Illumina [636870] 3 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST002741 Genome-wide genotyping array 2015-04-16 25082827 Julia A 2014-07-31 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25082827 A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis. Ulcerative colitis up to 7,483 European ancestry cases, up to 21,211 European ancestry controls 1,073 European ancestry cases, 1,279 European ancestry controls Illumina [546271] 9 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST002548 Genome-wide genotyping array 2015-04-23 25003214 Davis OS 2014-07-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25003214 The correlation between reading and mathematics ability at age twelve has a substantial genetic component. Reading or mathematical ability up to 2,794 European ancestry unrelated members of twin pairs 2,153 European ancestry individuals Affymetrix [1588650] (imputed) 2 reading, mathematical ability http://www.ebi.ac.uk/efo/EFO_0005229, http://www.ebi.ac.uk/efo/EFO_0004875 GCST002522 Genome-wide genotyping array 2015-09-23 25562672 Byrne EM 2014-12-09 J Clin Psychiatry www.ncbi.nlm.nih.gov/pubmed/25562672 Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder. Seasonality 3,269 European ancestry individuals 887 Old order Amish individuals Affymetrix, Illumina [2354422] (imputed) 8 seasonality measurement http://www.ebi.ac.uk/efo/EFO_0006876 GCST002719 Genome-wide genotyping array 2014-11-18 24847357 Ye Z 2014-05-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/24847357 Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections. Staphylococcus aureus infection 309 European ancestry cases, 2,925 European ancestry controls NA Illumina [508921] 4 Staphylococcus aureus infection http://www.ebi.ac.uk/efo/EFO_0005681 GCST002440 Genome-wide genotyping array 2008-09-10 17684544 Franke A 2007-08-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/17684544 Systematic association mapping identifies NELL1 as a novel IBD disease gene. Crohn's disease 393 European ancestry cases, 399 European ancestry controls 375 European ancestry trios, 1,395 European ancestry cases, 1,603 European ancestry controls, 454 French Canadian founder trios, 466 French Canadian founder cases, 358 French Canadian founder controls Affymetrix [92387] 3 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000066 Genome-wide genotyping array 2014-06-28 24277619 Quillen EE 2013-11-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/24277619 ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sample. Alcohol dependence 102 Han Chinese ancestry cases, 212 Han Chinese ancestry controls NA Illumina [247725] 2 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST002293 Genome-wide genotyping array 2014-06-28 24277619 Quillen EE 2013-11-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/24277619 ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sample. Response to alcohol consumption (flushing response) 108 Han Chinese ancestry cases, 190 Han Chinese ancestry controls NA Illumina [247725] 3 response to alcohol http://www.ebi.ac.uk/efo/EFO_0005526 GCST002292 Genome-wide genotyping array 2014-06-28 24277619 Quillen EE 2013-11-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/24277619 ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sample. Alcohol consumption (max-drinks) 272 Han Chinese ancestry individuals NA Illumina [247725] 3 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST002294 Genome-wide genotyping array 2014-11-26 24832863 Wetherill L 2014-05-16 Addict Biol www.ncbi.nlm.nih.gov/pubmed/24832863 Association of substance dependence phenotypes in the COGA sample. Substance dependence phenotypes up to 2,322 European ancestry individuals from 118 families 2,647 European ancestry individuals Illumina [591785] 0 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST002452 Genome-wide genotyping array 2015-10-24 25561047 Musani SK 2015-01-05 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25561047 Genome-wide association analysis of plasma B-type natriuretic peptide in blacks: the Jackson Heart Study. B-type natriuretic peptide levels 2,790 Black individuals NA Affymetrix [2500000] (imputed) 2 BNP measurement http://www.ebi.ac.uk/efo/EFO_0006920 GCST002736 Genome-wide genotyping array 2013-11-20 23726668 Hunter AM 2013-05-30 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/23726668 A genome-wide association study of a sustained pattern of antidepressant response. Response to antidepressant treatment (citalopram) 869 European, Hispanic, African American, Asian, mixed race and other ancestry sustained response individuals, 247 European, Hispanic, African American, Asian, mixed race and other ancestry unsustained response individuals 394 European ancestry sustained response individuals, 191 European ancestry unsustained response individuals Affymetrix [430198] 3 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST002046 Genome-wide genotyping array 2015-06-02 25102180 Ng MC 2014-08-07 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25102180 Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes. Type 2 diabetes 8,284 African American cases, 15,543 African American controls 6,061 African American cases, 5,483 African American controls, 8,130 European ancestry cases, 38,987 European ancestry controls Affymetrix, Illumina [2579389] (imputed) 20 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002560 Genome-wide genotyping array 2015-05-22 25343990 Cornelis MC 2014-10-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25343990 Genome-wide association study of selenium concentrations. Toenail selenium levels 4,162 European ancestry individuals NA Affymetrix, Illumina [2378986] (imputed) 16 selenium measurement http://www.ebi.ac.uk/efo/EFO_0006331 GCST002671 Genome-wide genotyping array 2015-07-08 25343990 Cornelis MC 2014-10-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25343990 Genome-wide association study of selenium concentrations. Blood and toenail selenium levels 9,639 European ancestry individuals NA Affymetrix, Illumina [2379663] (imputed) 12 selenium measurement http://www.ebi.ac.uk/efo/EFO_0006331 GCST002670 Genome-wide genotyping array 2013-11-20 23708191 Cordell HJ 2013-05-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23708191 Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. Congenital heart disease 1,479 European ancestry congenital heart disease cases, 340 European ancestry ostium secundum atrial septal defect cases, 5,159 European ancestry controls 417 European ancestry ostium secundum atrial septal defect cases, 209 European ancestry ventricular septal defect cases, 2,520 European ancestry controls Illumina [514952] 2 congenital heart disease http://www.ebi.ac.uk/efo/EFO_0005207 GCST002035 Genome-wide genotyping array 2014-04-15 24172245 Haga S 2013-10-31 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24172245 A genome-wide association study of third molar agenesis in Japanese and Korean populations. Tooth agenesis (maxillary third molar) 125 East Asian ancestry maxillary cases, 24 East Asian ancestry mandibular cases, 338 East Asian ancestry controls NA Illumina [532105] 0 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST002257 Genome-wide genotyping array 2014-04-15 24172245 Haga S 2013-10-31 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24172245 A genome-wide association study of third molar agenesis in Japanese and Korean populations. Tooth agenesis (mandibular third molar) 80 East Asian ancestry mandibular cases, 69 East Asian ancestry maxillary cases, 338 East Asian ancestry controls NA Illumina [532105] 2 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST002258 Genome-wide genotyping array 2014-04-15 24172245 Haga S 2013-10-31 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24172245 A genome-wide association study of third molar agenesis in Japanese and Korean populations. Tooth agenesis (third molar) 149 East Asian ancestry cases, 338 East Asian ancestry controls NA Illumina [532105] 1 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST002256 Genome-wide genotyping array 2014-04-15 24152035 Goodbourn PT 2013-10-23 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24152035 Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia. Contrast sensitivity 985 European ancestry individuals NA Illumina [642758] 5 contrast sensitivity measurement http://www.ebi.ac.uk/efo/EFO_0005419 GCST002238 Genome-wide genotyping array 2014-03-25 24026423 Shameer K 2013-09-12 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24026423 A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. Platelet count 13,582 European ancestry individuals NA Illumina [476395] 8 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST002186 Genome-wide genotyping array 2014-03-25 24026423 Shameer K 2013-09-12 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24026423 A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. Mean platelet volume 6,291 European ancestry individuals NA Illumina [476395] 11 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST002184 Genome-wide genotyping array 2013-11-20 23717212 Band G 2013-05-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23717212 Imputation-based meta-analysis of severe malaria in three African populations. Malaria 5,425 African ancestry cases, 6,891 African ancestry controls NA Illumina [1300000] (imputed) 6 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST002033 Genome-wide genotyping array 2008-06-16 17804789 Raelson JV 2007-09-05 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/17804789 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. Crohn's disease 382 French Canadian founder trios 750 European ancestry cases, 828 European ancestry controls, 521 European ancestry trios Perlegen [164279] 3 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST000071 Genome-wide genotyping array 2014-05-03 24166486 Sleiman P 2013-10-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/24166486 GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus. Schizophrenia, schizoaffective disorder or bipolar disorder 11,985 European, African American, Asian, other and unknown ancestry schizophrenia cases, 377 European, African American, Asian, other and unknown ancestry schizoaffective disorder cases, 1,032 bipolar disorder cases, 34,676 European, African American, Asian, other and unknown ancestry controls 2652 individuals Affymetrix, Illumina [NR] (imputed) 5 bipolar disorder, schizophrenia, schizoaffective disorder http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0005411 GCST002254 Genome-wide genotyping array 2015-12-18 25581431 Kuchenbaecker KB 2015-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25581431 Identification of six new susceptibility loci for invasive epithelial ovarian cancer. Epithelial ovarian cancer 4,368 European ancestry cases, 9,123 European ancestry controls, 2,462 European ancestry BRCA1 mutation carrier cases, 12,790 European ancestry BRCA1 mutation carrier controls, up to 631 European ancestry BRCA2 mutation carrier cases, 7,580 European ancestry BRCA2 mutation carrier controls, 9,627 European ancestry serous cases, 1,442 European ancestry non-serous cases, 21,722 European ancestry controls Illumina [up to 10962898] (imputed) 21 malignant epithelial tumor of ovary http://purl.obolibrary.org/obo/MONDO_0018364 GCST002748 Genome-wide genotyping array 2015-10-27 25583994 Tardif JC 2015-01-11 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25583994 Pharmacogenomic determinants of the cardiovascular effects of dalcetrapib. Response to Dalcetrapib treatment in acute coronary syndrome 2,845 European ancestry individuals NA Illumina [5543264] (imputed) 1 response to dalcetrapib, cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0006916, http://www.ebi.ac.uk/efo/EFO_0006919 GCST002747 Genome-wide genotyping array 2015-02-19 24916650 Versmissen J 2014-06-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24916650 Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach. Coronary heart disease in familial hypercholesterolemia 249 European ancestry cases, 217 European ancestry controls 744 European ancestry cases, 1,691 European ancestry controls Illumina [535179] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST002478 Genome-wide genotyping array 2015-05-18 24141364 Perez-Andreu V 2013-10-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24141364 Inherited GATA3 variants are associated with Ph-like childhood acute lymphoblastic leukemia and risk of relapse. Acute lymphoblastic leukemia (childhood) 75 European, Asian, African American, and Hispanic ancestry Ph-like ALL cases, 436 European, Asian, African American, and Hispanic ancestry non Ph-like ALL cases, 6,661 European, Asian, African American, and Hispanic ancestry non-ALL controls 32 European, Asian, African American, and Hispanic ancestry Ph-like ALL cases, 139 European, Asian, African American, and Hispanic ancestry non Ph-like ALL cases, 3,647 European ancestry non-ALL controls, 1,228 African American non-ALL controls, 920 Hispanic non-ALL controls, 25 Native American non-ALL controls Affymetrix [up to 761049] 0 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST002236 Genome-wide genotyping array 2015-05-16 25327703 Fejerman L 2014-10-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25327703 Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25. Breast cancer 1,497 Latino cases, 3,213 Latino controls 1,643 Latino cases, 4,971 Latino controls Affymetrix, Illumina [7229558] (imputed) 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST002662 Genome-wide genotyping array 2015-05-29 25317111 Seo I 2014-09-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/25317111 Genome-wide association study of medication adherence in chronic diseases in the korean population. Medication adherence in chronic diseases 155 Korean ancestry medication non-adherent diabetes cases, 80 Korean ancestry medication non-adherent hypertensive cases, 240 Korean ancestry medication adherent diabetes cases, 827 Korean ancestry medication adherent hypertensive cases NA NR [349184] 2 medication adherence behavior http://www.ebi.ac.uk/efo/EFO_0006344 GCST002637 Genome-wide genotyping array 2014-04-10 24121790 Levine DM 2013-10-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24121790 A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. Esophageal adenocarcinoma 1,516 European ancestry cases, 3,209 European ancestry controls 874 European ancestry cases, 6,911 European ancestry controls Illumina [922031] 8 esophageal adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000478 GCST002232 Genome-wide genotyping array 2014-04-10 24121790 Levine DM 2013-10-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24121790 A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. Digestive system disease (Barrett's esophagus and esophageal adenocarcinoma combined) 3,928 European ancestry cases, 3,207 European ancestry controls 1,636 European ancestry cases, 6,911 European ancestry controls Illumina [922031] 10 esophageal adenocarcinoma, digestive system disease, Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000478, http://www.ebi.ac.uk/efo/EFO_0000405, http://www.ebi.ac.uk/efo/EFO_0000280 GCST002231 Genome-wide genotyping array 2014-04-10 24121790 Levine DM 2013-10-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24121790 A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus. Barrett's esophagus 2,416 European ancestry cases, 3,206 European ancestry controls 759 European ancestry cases, 6,911 European ancestry controls Illumina [922031] 7 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST002230 Genome-wide genotyping array 2015-06-23 25249183 Lu X 2014-09-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25249183 Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. Systolic blood pressure 11,816 Han Chinese ancestry individuals 69,146 Han Chinese ancestry individuals Affymetrix, Illumina [2485448] (imputed) 15 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST002630 Genome-wide genotyping array 2015-06-23 25249183 Lu X 2014-09-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25249183 Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. Diastolic blood pressure 11,816 Han Chinese ancestry individuals 69,146 Han Chinese ancestry individuals Affymetrix, Illumina [2485448] (imputed) 14 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST002631 Genome-wide genotyping array 2015-06-23 25249183 Lu X 2014-09-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25249183 Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension. Hypertension 5,065 Han Chinese ancestry cases, 4,404 Han Chinese ancestry controls 29,799 Han Chinese ancestry cases, 39,347 Han Chinese ancestry controls Affymetrix, Illumina [2485448] (imputed) 12 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST002627 Genome-wide genotyping array 2014-12-14 24927181 Navarini AA 2014-06-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24927181 Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris. Acne (severe) 1,893 European ancestry cases, 5,132 European ancestry controls 2,063 European ancestry cases, 1,970 European ancestry controls Illumina [7300000] (imputed) 14 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST002481 Genome-wide genotyping array 2015-05-11 22005931 Kamboh MI 2011-10-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22005931 Genome-wide association analysis of age-at-onset in Alzheimer's disease. Alzheimer's disease (age of onset) 1,190 European ancestry cases, 1,032 cases NA Illumina [2543888] (imputed) 13 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST001280 Genome-wide genotyping array 2015-10-27 25562107 Israel E 2015-03-01 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/25562107 Genome-wide association study of short-acting β2-agonists. A novel genome-wide significant locus on chromosome 2 near ASB3. Bronchodilator response in asthma 724 European ancestry individuals 439 European ancestry individuals Affymetrix [444088] 1 response to bronchodilator http://purl.obolibrary.org/obo/GO_0097366 GCST002796 Genome-wide genotyping array 2015-12-18 25574825 Baurecht H 2015-01-08 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25574825 Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. Inflammatory skin disease 2,079 European ancestry atopic dermatitis cases, 4,212 European ancestry psoriasis cases, 11,899 European ancestry controls NA Affymetrix, Illumina [~ 5200000] 88 inflammatory skin disease http://www.ebi.ac.uk/efo/EFO_1000636 GCST002740 Genome-wide genotyping array 2016-01-12 25574825 Baurecht H 2015-01-08 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25574825 Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. Atopic dermatitis 2,079 European ancestry cases, 3,867 European ancestry controls NA Affymetrix, Illumina, Perlegen [up to 5493100] (imputed) 7 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST002737 Genome-wide genotyping array 2016-01-06 25574825 Baurecht H 2015-01-08 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25574825 Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. Psoriasis 4,212 European ancestry cases, 8,032 European ancestry controls NA Affymetrix, Illumina, Perlegen [up to 5493100] (imputed) 20 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST002738 Genome-wide genotyping array 2015-06-13 25310577 Evans TJ 2014-10-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/25310577 Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. Acute lymphoblastic leukemia (childhood) 358 European ancestry cases, 1,192 European ancestry controls 441 European ancestry cases, 1,542 European ancestry controls Illumina [7162141] (imputed) 2 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST002657 Genome-wide genotyping array 2014-12-10 24909733 Cook-Sather SD 2014-06-05 Pain www.ncbi.nlm.nih.gov/pubmed/24909733 TAOK3, a novel genome-wide association study locus associated with morphine requirement and postoperative pain in a retrospective pediatric day surgery population. Morphine dose requirement in tonsillectomy and adenoidectomy surgery 277 European ancestry children, 241 African American children 75 European ancestry children, 70 African American children Illumina [509904] 1 response to morphine http://purl.obolibrary.org/obo/GO_0043278 GCST002472 Genome-wide genotyping array 2014-07-29 24376456 Simino J 2013-12-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/24376456 Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9. Pulse pressure (alcohol consumption interaction) up to 6,882 individuals NA Affymetrix [2500000] (imputed) 4 pulse pressure measurement, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0004329 GCST002310 Genome-wide genotyping array 2014-07-29 24376456 Simino J 2013-12-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/24376456 Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9. Systolic blood pressure (alcohol consumption interaction) up to 6,882 European ancestry individuals NA Affymetrix [2500000] (imputed) 11 systolic blood pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004329 GCST002307 Genome-wide genotyping array 2014-07-29 24376456 Simino J 2013-12-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/24376456 Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9. Diastolic blood pressure (alcohol consumption interaction) up to 6,882 European ancestry individuals NA Affymetrix [2500000] (imputed) 4 diastolic blood pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004329 GCST002309 Genome-wide genotyping array 2014-07-29 24376456 Simino J 2013-12-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/24376456 Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9. Mean arterial pressure (alcohol consumption interaction) up to 6,882 individuals NA Affymetrix [2500000] (imputed) 9 diastolic blood pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004329 GCST002308 Genome-wide genotyping array 2015-06-05 25240745 Lopez S 2014-09-18 Mitochondrion www.ncbi.nlm.nih.gov/pubmed/25240745 A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels. Mitochondrial DNA levels 173 European ancestry males and 213 European ancestry females from 21 families NA Illumina [283437] 21 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST002616 Genome-wide genotyping array 2014-11-21 24825563 McDonald ML 2014-05-13 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/24825563 Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease. Resting oxygen saturation in chronic osbtructive pulmonary disease (pulse oxymetry) 820 African American cases 4,568 European ancestry cases Illumina [6160662] (imputed) 2 oxygen saturation measurement http://www.ebi.ac.uk/efo/EFO_0005682 GCST002447 Genome-wide genotyping array 2009-06-17 19497516 Elmore JR 2009-06-06 J Vasc Surg www.ncbi.nlm.nih.gov/pubmed/19497516 Identification of a genetic variant associated with abdominal aortic aneurysms on chromosome 3p12.3 by genome wide association. Abdominal aortic aneurysm 123 cases, 112 controls 827 cases, 1,034 controls Affymetrix [306330] 0 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST000419 Genome-wide genotyping array 2014-11-27 24861552 Rafnar T 2014-05-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24861552 Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer. Urinary bladder cancer 1,670 European ancestry cases, 90,180 European ancestry controls 5,241 European ancestry cases, 10,456 European ancestry controls Illumina [34200000] (imputed) 2 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST002460 Genome-wide genotyping array 2014-11-01 24651765 Williams SR 2014-03-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24651765 Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke. Plasma homocysteine levels (post-methionine load test) 2,710 European and other ancestry individuals, 1,725 European ancestry individuals, 258 African ancestry individuals, 117 individuals NA Affymetrix, Illumina [up to 11000000] (imputed) 5 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST002391 Genome-wide genotyping array 2014-02-18 23935956 Pistis G 2013-07-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/23935956 Genome wide association analysis of a founder population identified TAF3 as a gene for MCHC in humans. Red blood cell traits 1,664 Val Borbera (founder/genetic isolate) individuals 619 Friuli Venezia Giulia (founder/genetic isolate) individuals, 16,145 European ancestry individuals Illumina [~ 2500000] (imputed) 4 mean corpuscular volume, mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004526, http://www.ebi.ac.uk/efo/EFO_0004527 GCST002109 Genome-wide genotyping array 2014-07-22 24220699 Gudmundsson J 2013-11-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24220699 A common variant at 8q24.21 is associated with renal cell cancer. Renal cell carcinoma 1,505 European ancestry cases, 67,725 European ancestry controls 906 European ancestry cases, 3,772 European ancestry controls Illumina [785863] (imputed) 1 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST002273 Genome-wide genotyping array 2009-04-22 19359265 Mangino M 2009-04-08 J Med Genet www.ncbi.nlm.nih.gov/pubmed/19359265 A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length. Telomere length 1,625 European ancestry females 1,165 European ancestry individuals Illumina [~ 314075] 1 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST000376 Genome-wide genotyping array 2014-01-07 23770605 Berndt SI 2013-06-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23770605 Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia. Chronic lymphocytic leukemia 2,179 European ancestry cases, 6,221 European ancestry controls 1,709 European ancestry cases, 6,318 European ancestry controls Illumina [549934] 21 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST002073 Genome-wide genotyping array 2015-04-23 25138779 Mitchell LE 2014-08-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25138779 Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations. Congenital left-sided heart lesions (maternal effect) 284 European ancestry case-parent trios, up to 93 case-parent trios 216 European ancestry case-parent trios, 8 case-parent trios Illumina [1712604] (imputed) 1 congenital left-sided heart lesions, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005938, http://www.ebi.ac.uk/efo/EFO_0005939 GCST002574 Genome-wide genotyping array 2015-04-23 25138779 Mitchell LE 2014-08-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25138779 Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations. Congenital left-sided heart lesions 284 European ancestry case-parent trios, up to 93 case-parent trios 216 European ancestry case-parent trios, 8 case-parent trios Illumina [1712604] (imputed) 3 congenital left-sided heart lesions http://www.ebi.ac.uk/efo/EFO_0005938 GCST002572 Genome-wide genotyping array 2014-10-15 24574247 Yuan H 2014-02-25 Autism Res www.ncbi.nlm.nih.gov/pubmed/24574247 Investigation of maternal genotype effects in autism by genome-wide association. Maternal genotype effects in autism spectrum disorder families 561 European, African American, Asian and other ancestry mothers of autism cases, 547 European, African American, Asian and other ancestry fathers of autism cases, 508 European ancestry females 982 European and other ancestry mothers of autism cases, 1,007 European and other ancestry fathers of autism cases, 743 European and other ancestry females Illumina [1776310] (imputed) 0 autism spectrum disorder, genetic variation http://www.ebi.ac.uk/efo/EFO_0003756, http://www.ebi.ac.uk/efo/EFO_0004828 GCST002368 Genome-wide genotyping array 2010-01-21 20066028 Igl W 2010-01-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20066028 Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. Cholesterol 656 European ancestry individuals Up to 3,282 European ancestry individuals Illumina [~ 311388] 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST000559 Genome-wide genotyping array 2015-06-19 25201287 Del-Aguila JL 2014-09-09 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/25201287 Transethnic meta-analysis suggests genetic variation in the HEME pathway influences potassium response in patients treated with hydrochlorothiazide. Response to thiazide diuretic treatment (hypokalemia) 425 European ancestry hypertensive individuals, 342 African American hypertensive individuals NA Illumina [> 2000000] (imputed) 0 response to hydrochlorothiazide, Hypokalemia http://www.ebi.ac.uk/efo/EFO_0005202, http://purl.obolibrary.org/obo/HP_0002900 GCST002600 Genome-wide genotyping array 2014-10-17 24621683 Cho MH 2014-02-07 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/24621683 Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis. Chronic obstructive pulmonary disease (moderate to severe) 5,812 European ancestry cases, 3,955 European ancestry controls, 821 African American cases, 1,749 African American controls 2,651 cases and their relatives Illumina [up to 701491] (imputed) 9 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST002351 Genome-wide genotyping array 2014-10-17 24621683 Cho MH 2014-02-07 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/24621683 Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis. Chronic obstructive pulmonary disease (severe) 3,145 European ancestry cases, 3,955 European ancestry controls, 352 African American cases, 1,749 African American controls 2,651 cases and their relatives Illumina [up to 701491] (imputed) 6 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST002350 Genome-wide genotyping array 2015-05-16 25248455 Ek WE 2014-09-23 Gut www.ncbi.nlm.nih.gov/pubmed/25248455 Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts. Irritable bowel syndrome 534 European ancestry cases, 4,932 European ancestry controls 1,718 European ancestry cases, 1,793 European ancestry controls Illumina [1253036] (imputed) 2 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST002629 Genome-wide genotyping array 2014-10-09 24465431 Ma RC 2014-01-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/24465431 Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese. Type 2 diabetes (young onset) and obesity 99 Chinese ancestry cases, 101 Chinese ancestry controls NA Illumina [425513] 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002339 Genome-wide genotyping array 2015-02-03 25008200 Feng P 2014-07-09 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/25008200 Genome wide association scan for chronic periodontitis implicates novel locus. Chronic periodontitis 63 European ancestry cases, 543 European ancestry controls, up to 32 African American cases, up to 158 African American controls, up to 4 cases, up to 66 controls 495 European ancestry cases, 981 European ancestry controls, 118 African ancestry cases, 225 African ancestry controls Illumina [473514] 2 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST002524 Genome-wide genotyping array 2015-04-01 25042611 Griffin PJ 2014-07-19 Am J Hematol www.ncbi.nlm.nih.gov/pubmed/25042611 The genetics of hemoglobin A2 regulation in sickle cell anemia. Hemoglobin A2 levels in sickle cell anemia 618 African American cases 173 African American cases, 398 Chinese ancestry individuals Illumina [NR] 3 hemoglobin A2 measurement http://www.ebi.ac.uk/efo/EFO_0005845 GCST002536 Genome-wide genotyping array 2014-11-01 24647736 Chen P 2014-03-19 Diabetes www.ncbi.nlm.nih.gov/pubmed/24647736 Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians. Glycated hemoglobin levels 17,290 East Asian ancestry individuals, 1,727 Malay ancestry individuals up to 13,585 East Asian ancestry individuals Affymetrix, Illumina [up to 2400000] (imputed) 12 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST002390 Genome-wide genotyping array 2014-10-14 24839885 Benke KS 2014-02-19 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/24839885 A genome-wide association meta-analysis of preschool internalizing problems. Preschool internalizing problems 3,121 European ancestry individuals, 1,475 children from 1,031 families NA Affymetrix, Illumina [2403520] (imputed) 13 Child Behaviour Checklist assessment http://www.ebi.ac.uk/efo/EFO_0005661 GCST002362 Genome-wide genotyping array 2009-09-09 19698717 Cui R 2009-08-18 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/19698717 Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. Esophageal cancer 182 Japanese ancestry cases, 927 Japanese ancestry controls 782 Japanese ancestry cases, 1,898 Japanese ancestry controls Illumina [359195] 2 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST000466 Genome-wide genotyping array 2011-01-04 21059989 Lee JH 2010-11-08 Arch Neurol www.ncbi.nlm.nih.gov/pubmed/21059989 Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals. Alzheimer's disease 549 Caribbean Hispanic cases, 544 Caribbean Hispanic controls 3,839 European ancestry individuals, 116 Caribbean Hispanic cases, 70 Caribbean Hispanic controls Illumina [627380] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000864 Genome-wide genotyping array 2015-07-07 25376901 Munir MS 2014-11-05 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25376901 Genetic markers associated with plasma protein C level in African Americans: the atherosclerosis risk in communities (ARIC) study. Protein C levels 2,701 African American individuals NA Affymetrix [2649157] 4 protein C measurement http://www.ebi.ac.uk/efo/EFO_0004633 GCST002686 Genome-wide genotyping array 2015-01-21 24880342 Wang Y 2014-06-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24880342 Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer. Lung cancer 3,442 European ancestry adenocarcinoma cases, 3,275 European ancestry squamous cell carcinoma cases, 4,631 cases, up to 15,861 controls 3,589 European ancestry adenocarcinoma cases, 3,202 European ancestry squamous cell carcinoma cases, 3,455 cases, up to 38,295 controls Illumina [8900000] (imputed) 5 lung carcinoma, squamous cell carcinoma, lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0000707, http://www.ebi.ac.uk/efo/EFO_0000571 GCST002466 Genome-wide genotyping array 2014-10-17 24493630 Ahsan H 2014-02-03 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/24493630 A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age. Breast cancer (early onset) 3,523 European ancestry young female cases, 2,702 European ancestry young female controls 3,470 European ancestry young female cases, 5,475 European ancestry young female controls Illumina [1265548] (imputed) 18 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST002346 Genome-wide genotyping array 2015-05-23 24903457 Kim YK 2014-06-05 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/24903457 Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions. Blood pressure (anthropometric measures interaction) 7,486 Korean ancestry individuals 4,544 East Asian ancestry individuals Affymetrix [1573409] (imputed) 2 anthropometric measurement, diastolic blood pressure, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0004302, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335 GCST002471 Genome-wide genotyping array 2017-09-12 24903457 Kim YK 2014-06-05 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/24903457 Identification of a genetic variant at 2q12.1 associated with blood pressure in East Asians by genome-wide scan including gene-environment interactions. Blood pressure 7,486 Korean ancestry individuals 4,544 East Asian ancestry individuals Affymetrix [1573409] (imputed) 2 diastolic blood pressure, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335 GCST004705 Genome-wide genotyping array 2014-11-26 24824216 Myers RA 2014-05-13 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24824216 Genome-wide interaction studies reveal sex-specific asthma risk alleles. Asthma (sex interaction) 1,052 European ancestry male cases, 1,019 European ancestry female cases, 709 European ancestry male controls, 826 European ancestry female controls, 675 African American/African Caribbean male cases, 837 African American/African Caribbean female cases, 577 African American/African Caribbean male controls, 926 African American/African Caribbean female controls, 926 Latino male cases, 710 Latino female cases, 410 Latino male controls, 382 Latino female controls NA Affymetrix, Illumina [~ 2100000] (imputed) 6 asthma, sex interaction measurement http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0008343 GCST002445 Genome-wide genotyping array 2014-10-08 24406073 Galanter JM 2014-01-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/24406073 Genome-wide association study and admixture mapping identify different asthma-associated loci in Latinos: the Genes-environments & Admixture in Latino Americans study. Asthma 1,893 Latin American cases, 1,881 Latin American controls EVE Asthma Consortium, see Torgerson et al., 2011 Affymetrix [747129] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST002330 Genome-wide genotyping array 2014-10-28 24656865 Woo D 2014-03-18 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24656865 Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. Intracerebral hemorrhage 664 European ancestry lobar cases, 881 European ancestry nonlobar cases, 1,481 European ancestry controls 513 European ancestry cases, 634 African American cases, 534 Hispanic cases, 1,552 European ancestry controls, 449 African American controls, 260 Hispanic controls Affymetrix, Illumina [5258103] (imputed) 1 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST002389 Genome-wide genotyping array 2008-09-15 18282107 Shifman S 2008-02-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/18282107 Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. Schizophrenia 660 Ashkenazi Jewish cases, 2,271 Ashkenazi Jewish controls 1,859 European ancestry cases, 3,943 European ancestry controls, 759 Ashkenazi Jewish cases, 3,389 Ashkenazi Jewish controls, 415 Han Chinese ancestry cases, 458 Han Chinese ancestry controls Affymetrix [510552] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST000155 Genome-wide genotyping array 2009-02-14 16614226 Herbert A 2006-04-14 Science www.ncbi.nlm.nih.gov/pubmed/16614226 A common genetic variant is associated with adult and childhood obesity. Obesity 694 individuals from 288 families 3,213 European ancestry obese cases, 6,210 European ancestry non-obese controls, 229 individuals, 368 European ancestry trios, 361 African American obese cases, 505 African American non-obese controls Affymetrix [86604] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST000003 Genome-wide genotyping array 2014-07-26 24324648 Yatagai Y 2013-12-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/24324648 Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population. IgE levels 967 Japanese ancestry individuals, 213 Japanese ancestry asthmatic individuals 1,894 Japanese ancestry individuals, 580 Japanese ancestry asthmatic individuals Illumina [479940] 1 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST002302 Genome-wide genotyping array 2008-08-07 18650507 Link E 2008-07-23 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/18650507 SLCO1B1 variants and statin-induced myopathy--a genomewide study. Response to statin therapy 85 European ancestry cases, 90 European ancestry controls 21 European ancestry cases, 16,643 European ancestry controls Illumina [316184] 1 response to statin http://purl.obolibrary.org/obo/GO_0036273 GCST000213 Genome-wide genotyping array 2011-06-04 21606135 Wild PS 2011-05-23 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/21606135 A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Coronary heart disease 2,078 European ancestry cases, 2,953 European ancestry controls 19,350 European ancestry cases, 35,408 European ancestry controls Affymetrix [608247] 5 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST001079 Genome-wide genotyping array 2014-11-06 24728293 Styrkarsdottir U 2014-04-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24728293 Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31. Osteoarthritis (hand, severe) 623 European ancestry cases, 69,153 European ancestry controls 214 European ancestry cases, 8,172 European ancestry controls Illumina [34200000] (imputed) 1 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST002410 Genome-wide genotyping array 2015-01-20 25009551 Kullo IJ 2014-06-25 Front Genet www.ncbi.nlm.nih.gov/pubmed/25009551 The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study. Peripheral artery disease 1,641 European ancestry cases, 1,604 European ancestry controls 740 European ancestry cases, 1,501 European ancestry controls Illumina [537872] 3 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST002504 Genome-wide genotyping array 2014-11-01 24595857 Sandholm N 2014-03-05 Diabetologia www.ncbi.nlm.nih.gov/pubmed/24595857 Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes. Urinary albumin excretion rate in type 1 diabetes 1,925 European ancestry cases 3,750 European ancestry cases Illumina [2400000] (imputed) 2 urinary albumin excretion rate http://www.ebi.ac.uk/efo/EFO_0005667 GCST002382 Genome-wide genotyping array 2008-12-09 18941528 Comabella M 2008-10-22 PLoS One www.ncbi.nlm.nih.gov/pubmed/18941528 Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms. Multiple sclerosis 242 European ancestry cases, 242 European ancestry controls 553 European ancestry cases, 1,033 European ancestry controls Affymetrix [428867] 1 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST000252 Genome-wide genotyping array 2011-01-15 21173776 de Moor MH 2010-12-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21173776 Meta-analysis of genome-wide association studies for personality. Openness 17,375 European ancestry individuals 3,294 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 1 openness measurement http://www.ebi.ac.uk/efo/EFO_0007914 GCST000922 Genome-wide genotyping array 2018-09-24 21173776 de Moor MH 2010-12-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21173776 Meta-analysis of genome-wide association studies for personality. Conscientiousness 17,375 European ancestry individuals 3,294 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 1 conscientiousness measurement http://www.ebi.ac.uk/efo/EFO_0007912 GCST006326 Genome-wide genotyping array 2018-09-24 21173776 de Moor MH 2010-12-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21173776 Meta-analysis of genome-wide association studies for personality. Neuroticism 17,375 European ancestry individuals 3,294 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST006327 Genome-wide genotyping array 2018-09-24 21173776 de Moor MH 2010-12-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21173776 Meta-analysis of genome-wide association studies for personality. Extraversion 17,375 European ancestry individuals 3,294 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 0 extraversion measurement http://www.ebi.ac.uk/efo/EFO_0007913 GCST006328 Genome-wide genotyping array 2018-09-24 21173776 de Moor MH 2010-12-21 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21173776 Meta-analysis of genome-wide association studies for personality. Agreeableness 17,375 European ancestry individuals 3,294 European ancestry individuals Affymetrix, Illumina, Perlegen [~ 2500000] (imputed) 0 agreeableness measurement http://www.ebi.ac.uk/efo/EFO_0007915 GCST006329 Genome-wide genotyping array 2014-06-26 24236485 Cornejo-Garcia JA 2013-11-01 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/24236485 Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations. Acute urticaria and angioedema (non-steroidal anti-inflammatory drug-induced) 112 European ancestry cases, 124 European ancestry controls, 120 Han Chinese ancestry cases, 101 Han Chinese ancestry controls NA Affymetrix [up to 644046] 9 urticaria, response to non-steroidal anti-inflammatory, angioedema http://www.ebi.ac.uk/efo/EFO_0005531, http://www.ebi.ac.uk/efo/EFO_0005533, http://www.ebi.ac.uk/efo/EFO_0005532 GCST002263 Genome-wide genotyping array 2008-11-12 18821564 Mick E 2008-09-26 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18821564 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. Attention deficit hyperactivity disorder 105 European ancestry cases, 34 Hispanic cases, 26 African American cases, 22 cases NA Affymetrix [319722] 2 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST000235 Genome-wide genotyping array 2014-05-13 24223155 Behr ER 2013-11-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/24223155 Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes. Drug-induced torsades de pointes 216 European ancestry cases, 386 European ancestry drug-exposed controls, 385 European ancestry population controls NA Illumina [3542142] (imputed) 1 torsades de pointes, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0005307, http://purl.obolibrary.org/obo/GO_0009410 GCST002269 Genome-wide genotyping array 2015-04-01 25017104 Kottyan LC 2014-07-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25017104 Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. Eosinophilic esophagitis 657 European ancestry cases, 9,296 European ancestry controls NA Illumina [1468075] 17 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST002527 Genome-wide genotyping array 2009-11-30 19875103 Aberg K 2009-10-27 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/19875103 Genomewide association study of movement-related adverse antipsychotic effects. Response to antipsychotic therapy (extrapyramidal side effects) 421 European ancestry schizophrenia cases, 214 African American schizophrenia cases, 103 schizophrenia cases NA Affymetrix [492000] 17 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST000514 Genome-wide genotyping array 2014-11-14 24821223 Mattheisen M 2014-05-13 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24821223 Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. Obsessive-compulsive disorder 1,406 cases and 1,489 controls from 1,065 families, 192 cases, 1,984 controls NA Illumina [549123] 2 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST002451 Genome-wide genotyping array 2015-06-11 25246029 DiStefano JK 2014-09-23 Acta Diabetol www.ncbi.nlm.nih.gov/pubmed/25246029 Genome-wide analysis of hepatic lipid content in extreme obesity. Hepatic lipid content in extreme obesity 1,868 European ancestry cases NA Illumina [605718] 4 hepatic lipid content measurement http://www.ebi.ac.uk/efo/EFO_0006506 GCST002632 Genome-wide genotyping array 2015-06-11 25246029 DiStefano JK 2014-09-23 Acta Diabetol www.ncbi.nlm.nih.gov/pubmed/25246029 Genome-wide analysis of hepatic lipid content in extreme obesity. Bilirubin levels in extreme obesity 1,868 European ancestry cases NA Illumina [605718] 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST002628 Genome-wide genotyping array 2013-11-20 21183627 Bouchard C 2010-12-23 J Appl Physiol (1985) www.ncbi.nlm.nih.gov/pubmed/21183627 Genomic predictors of the maximal O₂ uptake response to standardized exercise training programs. Maximal oxygen uptake response 470 European ancestry individuals from 99 families 295 individuals, 247 Black individuals from 105 families Illumina [324611] 0 maximal oxygen uptake measurement http://www.ebi.ac.uk/efo/EFO_0004887 GCST000926 Genome-wide genotyping array 2014-05-12 24096698 De Vivo I 2013-10-06 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24096698 Genome-wide association study of endometrial cancer in E2C2. Endometrial cancer up to 2,695 European ancestry cases, up to 2,777 European ancestry controls up to 3,235 cases, up to 12,059 controls Illumina [873935] 9 endometrial neoplasm http://www.ebi.ac.uk/efo/EFO_0004230 GCST002218 Genome-wide genotyping array 2014-05-12 24096698 De Vivo I 2013-10-06 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24096698 Genome-wide association study of endometrial cancer in E2C2. Endometrial cancer 2,695 European ancestry cases, 2,777 European ancestry controls 2,261 cases, 3,357 controls Illumina [873935] 0 endometrial neoplasm http://www.ebi.ac.uk/efo/EFO_0004230 GCST002215 Genome-wide genotyping array 2014-11-11 24792382 Park TJ 2014-04-30 Clin Chim Acta www.ncbi.nlm.nih.gov/pubmed/24792382 Genome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid. Response to inhaled corticosteroid treatment in asthma (change in FEV1) 189 Korean ancestry cases NA Illumina [430487] 10 FEV change measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0031960 GCST002432 Genome-wide genotyping array 2014-07-22 24244560 Chen P 2013-11-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/24244560 A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry. Glycated hemoglobin levels 3,427 Chinese ancestry individuals, 1,735 Malay ancestry individuals, 1,520 Asian Indian ancestry individuals NA Illumina [up to 2400000] (imputed) 3 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST002270 Genome-wide genotyping array 2015-06-22 25338677 Kariuki SN 2014-10-23 Genes Immun www.ncbi.nlm.nih.gov/pubmed/25338677 Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus. Interferon alpha levels in systemic lupus erythematosus 88 European ancestry high interferon alpha cases, 322 European ancestry low interferon alpha cases 715 European ancestry cases, 450 African American cases Illumina [291943] 8 interferon alpha measurement http://www.ebi.ac.uk/efo/EFO_0006517 GCST002666 Genome-wide genotyping array 2015-05-15 25186300 Terao C 2014-09-03 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/25186300 Association between antinuclear antibodies and the HLA class II locus and heterogeneous characteristics of staining patterns: the Nagahama study. Antinuclear antibody levels 3,185 Japanese ancestry individuals 3,963 Japanese ancestry individuals Illumina [303506] 1 antinuclear antibody measurement http://www.ebi.ac.uk/efo/EFO_0005949 GCST002585 Genome-wide genotyping array 2014-11-13 24770881 Nelson PT 2014-04-27 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/24770881 ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. Hippocampal sclerosis of aging 241 cases, 1,998 controls 122 cases, 305 controls NR [4913579] (imputed) 1 hippocampal sclerosis of aging http://www.ebi.ac.uk/efo/EFO_0005678 GCST002430 Genome-wide genotyping array 2014-11-13 24770881 Nelson PT 2014-04-27 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/24770881 ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. Alzheimer's disease 1443 cases and 99 controls NA NR [4913579] (imputed) 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002429 Genome-wide genotyping array 2015-08-14 25469926 Gottlieb DJ 2014-12-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25469926 Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study. Sleep duration 47,180 European ancestry individuals 4,771 African American individuals Affymetrix, Illumina [2033301] 13 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST002711 Genome-wide genotyping array 2010-01-07 20029952 Sebastiani P 2009-10-23 Am J Hematol www.ncbi.nlm.nih.gov/pubmed/20029952 Genetic modifiers of the severity of sickle cell anemia identified through a genome-wide association study. Sickle cell anemia (severity) 177 African American severe cases, 1,088 African American mild cases 68 African American severe cases, 95 African American mild cases Illumina [~ 600000] 0 sickle cell anemia http://purl.obolibrary.org/obo/MONDO_0011382 GCST000513 Genome-wide genotyping array 2014-08-02 24468470 Zhang C 2013-12-26 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/24468470 Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study. Cognitive decline (age-related) 5,765 European ancestry individuals, 890 African American individuals NA Illumina [1530316] 11 Mental deterioration http://purl.obolibrary.org/obo/HP_0001268 GCST002320 Genome-wide genotyping array 2015-05-29 25214527 Dube MP 2014-09-11 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25214527 CKM and LILRB5 are associated with serum levels of creatine kinase. Creatine kinase levels in statin users 3,412 European ancestry individuals 3,389 European ancestry individuals Illumina [3232779] (imputed) 2 response to statin, creatine kinase measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0004534 GCST002603 Genome-wide genotyping array 2014-11-06 24564958 St Pourcain B 2014-02-24 Mol Autism www.ncbi.nlm.nih.gov/pubmed/24564958 Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence. Social communication problems Up to 5,628 European ancestry individuals NA Illumina [2293137] (imputed) 17 social communication impairment http://www.ebi.ac.uk/efo/EFO_0005427 GCST002367 Genome-wide genotyping array 2014-04-01 24047820 St Pourcain B 2013-09-18 Mol Autism www.ncbi.nlm.nih.gov/pubmed/24047820 Common variation contributes to the genetic architecture of social communication traits. Social communication problems 5,584 European ancestry children 1,364 European ancestry children Illumina [~ 2500000] (imputed) 4 social communication impairment http://www.ebi.ac.uk/efo/EFO_0005427 GCST002194 Genome-wide genotyping array 2014-10-23 24677629 Wolf EJ 2014-03-27 Depress Anxiety www.ncbi.nlm.nih.gov/pubmed/24677629 A genome-wide association study of clinical symptoms of dissociation in a trauma-exposed sample. Post-traumatic stress disorder 484 European ancestry trauma-exposed individuals NA Illumina [1197702] 7 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST002401 Genome-wide genotyping array 2014-04-01 24002674 Ozel AB 2013-09-04 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24002674 Genome-wide association study and meta-analysis of intraocular pressure. Intraocular pressure 2,847 European ancestry primary open angle glaucoma cases, 3,389 European ancestry controls NA Illumina [466573] 10 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST002168 Genome-wide genotyping array 2009-02-28 19221038 Soranzo N 2009-02-12 Blood www.ncbi.nlm.nih.gov/pubmed/19221038 A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function. Mean platelet volume 1,221 individuals 7,365 individuals Affymetrix [361352] 1 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST000342 Genome-wide genotyping array 2015-02-05 25044411 Liao SY 2014-07-08 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25044411 Genome-wide association and network analysis of lung function in the Framingham Heart Study. Lung function (forced expiratory volume in 1 second) 2,698 European ancestry individuals NA Affymetrix [300895] 2 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST002521 Genome-wide genotyping array 2015-09-22 25524916 Palmer ND 2014-12-18 Diabetes www.ncbi.nlm.nih.gov/pubmed/25524916 Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium. Glucose homeostasis traits up to 4,176 Mexican American individuals NA Illumina [693128] 74 insulin metabolic clearance rate measurement, disposition index measurement, insulin sensitivity measurement, glucose homeostasis measurement, glucose effectiveness measurement, acute insulin response measurement http://www.ebi.ac.uk/efo/EFO_0006830, http://www.ebi.ac.uk/efo/EFO_0006832, http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0006896, http://www.ebi.ac.uk/efo/EFO_0006833, http://www.ebi.ac.uk/efo/EFO_0006831 GCST002726 Genome-wide genotyping array 2015-07-07 25281659 van der Valk RJ 2014-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25281659 A novel common variant in DCST2 is associated with length in early life and height in adulthood. Birth length 28,459 European ancestry individuals 16,145 European ancestry individuals, 280 Moroccan ancestry individuals, 284 Surinamese ancestry individuals, 319 Turkish ancestry individuals, 651 Chinese ancestry individuals Affymetrix, Illumina [2201971] (imputed) 6 body height at birth http://www.ebi.ac.uk/efo/EFO_0006784 GCST002644 Genome-wide genotyping array 2015-07-07 25281659 van der Valk RJ 2014-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25281659 A novel common variant in DCST2 is associated with length in early life and height in adulthood. Infant length 28,238 European ancestry individuals NA Affymetrix, Illumina [2193675] (imputed) 15 infant body height http://www.ebi.ac.uk/efo/EFO_0006785 GCST002646 Genome-wide genotyping array 2009-05-27 19430482 Kottgen A 2009-05-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19430482 Multiple loci associated with indices of renal function and chronic kidney disease. Renal function and chronic kidney disease 2,388 European ancestry cases, 17,489 European ancestry controls 1,932 cases, 19,534 controls Affymetrix, Illumina [~ 2500000] (imputed) 4 renal system measurement, chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0004742, http://www.ebi.ac.uk/efo/EFO_0003884 GCST000397 Genome-wide genotyping array 2015-09-22 25552591 Lieb W 2014-12-31 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25552591 Genome-wide association study for endothelial growth factors. Endothelial growth factor levels up to 3,574 European ancestry individuals up to 3,184 European ancestry individuals Affymetrix [~ 2500000] (imputed) 3 endothelial growth factor measurement, angiopoietin-2 receptor measurement, angiopoietin-2 measurement, hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006900, http://www.ebi.ac.uk/efo/EFO_0006902, http://www.ebi.ac.uk/efo/EFO_0006901, http://www.ebi.ac.uk/efo/EFO_0006903 GCST002731 Genome-wide genotyping array 2014-07-29 24405752 An P 2013-12-04 Metabolism www.ncbi.nlm.nih.gov/pubmed/24405752 Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS). Glycated hemoglobin levels 4,088 European ancestry non-diabetic elderly individuals up to 47,822 European ancestry non-diabetic elderly individuals Illumina [9250000] (imputed) 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST002303 Genome-wide genotyping array 2014-10-31 24675659 Hartiala J 2014-03-27 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/24675659 Comparative genome-wide association studies in mice and humans for trimethylamine N-oxide, a proatherogenic metabolite of choline and L-carnitine. Plasma trimethylamine N-oxide levels 1,973 European ancestry individuals 1,892 European ancestry individuals Affymetrix [2421770] (imputed) 0 plasma trimethylamine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0005691 GCST002400 Genome-wide genotyping array 2014-11-15 24823311 Guan W 2014-05-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24823311 Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium. Plasma omega-6 polyunsaturated fatty acid levels (gamma-linolenic acid) 8,631 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 10 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST002450 Genome-wide genotyping array 2014-11-15 24823311 Guan W 2014-05-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24823311 Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium. Plasma omega-6 polyunsaturated fatty acid levels (arachidonic acid) 8,631 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST002449 Genome-wide genotyping array 2014-11-15 24823311 Guan W 2014-05-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24823311 Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium. Plasma omega-6 polyunsaturated fatty acid levels (adrenic acid) 8,631 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 6 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST002448 Genome-wide genotyping array 2014-11-15 24823311 Guan W 2014-05-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24823311 Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium. Plasma omega-6 polyunsaturated fatty acid levels (linoleic acid) 8,631 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST002446 Genome-wide genotyping array 2014-11-15 24823311 Guan W 2014-05-13 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24823311 Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium. Plasma omega-6 polyunsaturated fatty acid levels (dihomo-gamma-linolenic acid) 8,631 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST002444 Genome-wide genotyping array 2015-04-01 25010111 Bolton JL 2014-07-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25010111 Genome wide association identifies common variants at the SERPINA6/SERPINA1 locus influencing plasma cortisol and corticosteroid binding globulin. Cortisol levels (plasma) 12,597 European ancestry individuals 2,795 European ancestry individuals Illumina [~ 2500000] 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST002526 Genome-wide genotyping array 2014-10-30 24676358 Viktorin A 2014-03-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24676358 IgA measurements in over 12 000 Swedish twins reveal sex differential heritability and regulatory locus near CD30L. Serum IgA levels 9,617 European ancestry individuals 2,785 European ancestry individuals Illumina [2226980] (imputed) 1 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST002402 Genome-wide genotyping array 2014-10-21 24604477 An P 2014-03-07 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24604477 Genome-wide association studies identified novel loci for non-high-density lipoprotein cholesterol and its postprandial lipemic response. Non-HDL cholesterol levels 928 European ancestry individuals 843 Old Order Amish individuals, 2,470 European ancestry individuals Affymetrix [2543887] (imputed) 0 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST002384 Genome-wide genotyping array 2010-09-24 20811658 Uhl GR 2010-08-24 Mol Med www.ncbi.nlm.nih.gov/pubmed/20811658 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. Smoking cessation 369 European ancestry individuals NA Affymetrix [905273] 1 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST000778 Genome-wide genotyping array 2010-08-30 20045101 Ferreira MA 2009-12-31 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20045101 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. CD4:CD8 lymphocyte ratio 2,538 European ancestry twins from 1,089 families 988 individuals from 550 families Illumina [529721] 1 CD4:CD8 lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0004839 GCST000553 Genome-wide genotyping array 2019-09-10 20045101 Ferreira MA 2009-12-31 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20045101 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. CD3-positive T-lymphocyte count 2,538 European ancestry twins from 1,089 families 988 individuals from 550 families Illumina [529721] 0 CD3-positive T-lymphocyte count http://www.ebi.ac.uk/efo/EFO_0010106 GCST008636 Genome-wide genotyping array 2019-09-10 20045101 Ferreira MA 2009-12-31 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20045101 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. CD4-positive T-lymphocyte count 2,538 European ancestry twins from 1,089 families 988 individuals from 550 families Illumina [529721] 0 CD4-positive T-lymphocyte count http://www.ebi.ac.uk/efo/EFO_0010105 GCST008637 Genome-wide genotyping array 2019-09-10 20045101 Ferreira MA 2009-12-31 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20045101 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. CD8-positive T-lymphocyte count 2,538 European ancestry twins from 1,089 families 988 individuals from 550 families Illumina [529721] 1 CD8-positive T-lymphocyte count http://www.ebi.ac.uk/efo/EFO_0010107 GCST008638 Genome-wide genotyping array 2019-09-10 20045101 Ferreira MA 2009-12-31 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20045101 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. CD19-positive B-lymphocyte count 2,538 European ancestry twins from 1,089 families 988 individuals from 550 families Illumina [529721] 0 CD19-positive B-lymphocyte count http://www.ebi.ac.uk/efo/EFO_0010108 GCST008639 Genome-wide genotyping array 2019-09-10 20045101 Ferreira MA 2009-12-31 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/20045101 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. CD56-positive NK-lymphocyte cell count 2,538 European ancestry twins from 1,089 families 988 individuals from 550 families Illumina [529721] 0 CD56-positive NK-lymphocyte cell count http://www.ebi.ac.uk/efo/EFO_0010109 GCST008640 Genome-wide genotyping array 2015-01-13 24940741 Chang SW 2014-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/24940741 A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. Chronic hepatitis B infection 321 Chinese ancestry cases, 304 Chinese ancestry controls 1,302 Chinese ancestry cases, 761 Chinese ancestry controls Illumina [456262] 5 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST002490 Genome-wide genotyping array 2015-04-01 25147783 Keene KL 2014-08-06 Front Public Health www.ncbi.nlm.nih.gov/pubmed/25147783 Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial. Vitamin B levels in ischemic stroke 1,725 European ancestry cases, 258 African ancestry cases, 117 cases NA Illumina [737081] 8 vitamin B measurement http://www.ebi.ac.uk/efo/EFO_0004843 GCST002559 Genome-wide genotyping array 2014-10-09 24486069 Park HW 2014-01-31 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/24486069 Genetic predictors associated with improvement of asthma symptoms in response to inhaled corticosteroids. Asthma (corticosteroid response) 124 European ancestry individuals 297 European ancestry individuals Illumina [440862] 2 response to corticosteroid http://purl.obolibrary.org/obo/GO_0031960 GCST002342 Genome-wide genotyping array 2015-09-14 25387704 Malone SM 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387704 Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. Electroencephalogram traits 2,383 European ancestry adolescents and 1,643 European ancestry adults from 1,613 families NA Illumina [527829] 27 theta wave measurement, delta wave measurement, alpha peak frequency measurement, alpha wave measurement, electroencephalogram measurement, beta wave measurement http://www.ebi.ac.uk/efo/EFO_0006873, http://www.ebi.ac.uk/efo/EFO_0006872, http://www.ebi.ac.uk/efo/EFO_0006883, http://www.ebi.ac.uk/efo/EFO_0006870, http://www.ebi.ac.uk/efo/EFO_0004357, http://www.ebi.ac.uk/efo/EFO_0006871 GCST002709 Genome-wide genotyping array 2008-08-08 18660810 Schormair B 2008-07-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/18660810 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Restless legs syndrome 628 European ancestry cases, 1,644 European ancestry controls 1,550 European ancestry cases, 2,269 European ancestry controls, 285 French Canadian founder cases, 842 French Canadian founder controls Affymetrix [208733] 2 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST000214 Genome-wide genotyping array 2008-06-16 17611496 Moffatt MF 2007-07-26 Nature www.ncbi.nlm.nih.gov/pubmed/17611496 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. Asthma 994 European ancestry cases, 1,243 European ancestry controls 200 European ancestry cases, 2,120 European ancestry controls Illumina [307328] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000061 Genome-wide genotyping array 2014-03-13 23942779 McGue M 2013-08-14 Behav Genet www.ncbi.nlm.nih.gov/pubmed/23942779 A genome-wide association study of behavioral disinhibition. Nicotine use 7,188 European ancestry individuals NA Illumina [527829] 6 nicotine use http://www.ebi.ac.uk/efo/EFO_0005430 GCST002135 Genome-wide genotyping array 2014-03-13 23942779 McGue M 2013-08-14 Behav Genet www.ncbi.nlm.nih.gov/pubmed/23942779 A genome-wide association study of behavioral disinhibition. Alcohol consumption 7,188 European ancestry individuals NA Illumina [527829] 2 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST002130 Genome-wide genotyping array 2014-03-13 23942779 McGue M 2013-08-14 Behav Genet www.ncbi.nlm.nih.gov/pubmed/23942779 A genome-wide association study of behavioral disinhibition. Alcohol dependence 7,188 European ancestry individuals NA Illumina [527829] 4 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST002134 Genome-wide genotyping array 2014-03-13 23942779 McGue M 2013-08-14 Behav Genet www.ncbi.nlm.nih.gov/pubmed/23942779 A genome-wide association study of behavioral disinhibition. Illicit drug use 7,188 European ancestry individuals NA Illumina [527829] 10 illegal drug consumption http://www.ebi.ac.uk/efo/EFO_0005431 GCST002133 Genome-wide genotyping array 2014-03-13 23942779 McGue M 2013-08-14 Behav Genet www.ncbi.nlm.nih.gov/pubmed/23942779 A genome-wide association study of behavioral disinhibition. Non-substance related behavioral disinhibition 7,188 European ancestry individuals NA Illumina [527829] 4 non-substance related disinhibited behaviour http://www.ebi.ac.uk/efo/EFO_0005432 GCST002132 Genome-wide genotyping array 2014-03-13 23942779 McGue M 2013-08-14 Behav Genet www.ncbi.nlm.nih.gov/pubmed/23942779 A genome-wide association study of behavioral disinhibition. Behavioural disinhibition (generation interaction) 3,852 European ancestry parents, 3,336 European ancestry offspring NA Illumina [527829] 20 nicotine use, generational effect measurement, illegal drug consumption, non-substance related disinhibited behaviour, alcohol drinking, alcohol dependence http://www.ebi.ac.uk/efo/EFO_0005430, http://www.ebi.ac.uk/efo/EFO_0008364, http://www.ebi.ac.uk/efo/EFO_0005431, http://www.ebi.ac.uk/efo/EFO_0005432, http://www.ebi.ac.uk/efo/EFO_0004329, http://purl.obolibrary.org/obo/MONDO_0007079 GCST002131 Genome-wide genotyping array 2014-08-02 24386095 Zhou L 2013-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/24386095 A genome wide association study identifies common variants associated with lipid levels in the Chinese population. Lipid traits 3,451 Han Chinese ancestry individuals 8,830 Han Chinese ancestry individuals Affymetrix, Illumina [up to 2249917] (imputed) 18 total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004612 GCST002321 Genome-wide genotyping array 2014-07-23 24189344 Xia K 2013-11-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24189344 Common genetic variants on 1p13.2 associate with risk of autism. Autism 275 Chinese ancestry cases and 550 Chinese ancestry controls from 275 trios, 136 Chinese ancestry cases, 984 Chinese ancestry controls 1,299 European ancestry cases and 2,598 European ancestry controls from 1,299 trios Illumina [702234] (imputed) 11 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST002268 Genome-wide genotyping array 2014-03-01 23903356 Hayes MG 2013-07-31 Diabetes www.ncbi.nlm.nih.gov/pubmed/23903356 Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies. Glycemic traits (pregnancy) 1,367 European ancestry individuals, 817 Hispanic individuals, 1,075 Afro-Caribbean individuals, 1,178 Thai ancestry individuals 2,798 European ancestry individuals, 228 French Canadian founder population individuals Illumina [up to 945994] (imputed) 10 C-peptide measurement, fasting blood glucose measurement, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0005187, http://www.ebi.ac.uk/efo/EFO_0004465, http://www.ebi.ac.uk/efo/EFO_0004307 GCST002110 Genome-wide genotyping array 2014-08-03 24357727 Rocanin-Arjo A 2013-12-19 Blood www.ncbi.nlm.nih.gov/pubmed/24357727 A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential. Thrombin generation potential phenotypes 714 European ancestry venous thrombosis cases, 1,253 European ancestry individuals 714 European ancestry venous thrombosis cases, 543 European ancestry individuals NR [6652054] (imputed) 4 thrombin generation potential measurement http://www.ebi.ac.uk/efo/EFO_0005538 GCST002315 Genome-wide genotyping array 2009-03-18 19242412 Gu Y 2009-02-25 Nature www.ncbi.nlm.nih.gov/pubmed/19242412 Identification of IFRD1 as a modifier gene for cystic fibrosis lung disease. Cystic fibrosis severity 160 European ancestry severe lung disease cases, European ancestry 160 mild lung disease cases 485 European ancestry cases,91 controls, 2,194 individuals Affymetrix [100198] 0 cystic fibrosis http://purl.obolibrary.org/obo/MONDO_0009061 GCST000346 Genome-wide genotyping array 2010-05-12 20400458 Kang SJ 2010-04-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20400458 Genome-wide association of anthropometric traits in African- and African-derived populations. Anthropometric traits 743 African American individuals, 1,188 Nigerian ancestry individuals 704 African American individuals from 306 families, 3,471 African American and Afro-Caribbean individuals Affymetrix [up to 2900000] (imputed) 0 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST000660 Genome-wide genotyping array 2015-04-16 25129146 Wu C 2014-08-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25129146 Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations. Esophageal squamous cell carcinoma 5,337 Han Chinese ancestry cases, 5,787 Han Chinese ancestry controls 9,654 Han Chinese ancestry cases, 10,058 Han Chinese ancestry controls Affymetrix, Illumina [7556215] (imputed) 10 esophageal squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0005922 GCST002568 Genome-wide genotyping array 2014-10-28 24665060 Argos M 2014-03-24 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24665060 Genome-wide association study of smoking behaviours among Bangladeshi adults. Smoking quantity 1,837 Bangladeshi ancestry males, 198 Bangladeshi ancestry females NA Illumina [1211988] (imputed) 8 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST002393 Genome-wide genotyping array 2014-10-28 24665060 Argos M 2014-03-24 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24665060 Genome-wide association study of smoking behaviours among Bangladeshi adults. Smoking initiation 754 Bangladeshi ancestry never smoker males, 2,565 Bangladeshi ancestry never smoker females, 1,837 Bangladeshi ancestry ever smoker males, 198 Bangladeshi ancestry ever smoker females NA Illumina [1211988] (imputed) 27 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST002396 Genome-wide genotyping array 2014-10-28 24665060 Argos M 2014-03-24 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24665060 Genome-wide association study of smoking behaviours among Bangladeshi adults. Age of smoking initiation 1,837 Bangladeshi ancestry males, 198 Bangladeshi ancestry females NA Illumina [1211988] (imputed) 8 age at onset, smoking initiation http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0005670 GCST002394 Genome-wide genotyping array 2014-10-28 24665060 Argos M 2014-03-24 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24665060 Genome-wide association study of smoking behaviours among Bangladeshi adults. Smoking cessation 366 Bangladeshi ancestry former smoker males, 87 Bangladeshi ancestry former smoker females, 1,471 Bangladeshi ancestry current smoker males, 111 Bangladeshi ancestry current smoker females NA Illumina [1211988] (imputed) 4 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST002395 Genome-wide genotyping array 2015-05-06 22055160 Bown MJ 2011-11-04 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22055160 Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1. Abdominal aortic aneurysm 1,737 European ancestry cases, 5,435 European ancestry controls, 129 cases 2,320 European ancestry cases, 40,011 European ancestry controls, 2,042 cases, 3,736 controls Illumina [535296] 1 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST001312 Genome-wide genotyping array 2015-01-20 24964207 Mullins N 2014-06-25 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/24964207 Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. Suicidal ideation in depression or bipolar disorder 237 European ancestry cases, 510 European ancestry controls NA Illumina [494742] 1 suicidal ideation http://www.ebi.ac.uk/efo/EFO_0004320 GCST002505 Genome-wide genotyping array 2015-01-20 24964207 Mullins N 2014-06-25 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/24964207 Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study. Suicide attempts in depression or bipolar disorder 426 European ancestry cases, 2,844 European ancestry controls NA Illumina [up to 503016] 3 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST002503 Genome-wide genotyping array 2011-01-06 21076409 Sotoodehnia N 2010-11-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21076409 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. QRS duration 39,717 European ancestry individuals, 690 Orcadian individuals 7,170 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 12 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST000872 Genome-wide genotyping array 2014-11-13 24768677 de Boer YS 2014-04-23 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/24768677 Genome-wide association study identifies variants associated with autoimmune hepatitis type 1. Autoimmune hepatitis type-1 649 European ancestry cases, 13,436 European ancestry controls 451 European ancestry cases, 4,103 European ancestry controls Illumina [254006] 3 Autoimmune Hepatitis http://www.ebi.ac.uk/efo/EFO_0005676 GCST002423 Genome-wide genotyping array 2014-10-01 24489884 Mick E 2014-01-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/24489884 Genome-wide association study of proneness to anger. Anger 8,747 European ancestry individuals NA Affymetrix [677643] 14 aggressive behavior http://www.ebi.ac.uk/efo/EFO_0003015 GCST002324 Genome-wide genotyping array 2014-10-01 24399259 He L 2014-01-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24399259 Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne. Acne (severe) 1,031 Han Chinese ancestry cases, 1,031 Han Chinese ancestry controls 1,860 Han Chinese ancestry cases, 3,660 Han Chinese ancestry controls Illumina [809305] 3 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST002329 Genome-wide genotyping array 2014-07-22 24220910 Purdue MP 2013-11-12 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/24220910 A genome-wide association study of renal cell carcinoma among African Americans. Renal cell carcinoma 255 African American cases, 375 African American controls 140 African American cases, 543 African American controls Illumina [1136723] 0 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST002272 Genome-wide genotyping array 2015-09-24 25282103 Wood AR 2014-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25282103 Defining the role of common variation in the genomic and biological architecture of adult human height. Height 253,288 European ancestry individuals 80,067 European ancestry individuals Affymetrix, Illumina, Perlegen [2550858] (imputed) 173 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST002647 Genome-wide genotyping array 2015-06-20 25245031 Luneburg N 2014-09-21 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25245031 Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine. L-arginine levels 3,747 European ancestry individuals, 2,992 individuals, 1,159 European ancestry individuals Affymetrix, Illumina [up to 2200000] (imputed) 1 L-arginine measurement http://www.ebi.ac.uk/efo/EFO_0006524 GCST002623 Genome-wide genotyping array 2015-06-20 25245031 Luneburg N 2014-09-21 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25245031 Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine. Asymmetrical dimethylarginine levels 3,742 European ancestry individuals, 2,992 individuals 1,151 European ancestry individuals Affymetrix, Illumina [up to 2200000] (imputed) 1 asymmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006522 GCST002620 Genome-wide genotyping array 2015-06-20 25245031 Luneburg N 2014-09-21 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25245031 Genome-wide association study of L-arginine and dimethylarginines reveals novel metabolic pathway for symmetric dimethylarginine. Symmetrical dimethylarginine levels 3,745 European ancestry individuals, 2,992 individuals 1,152 European ancestry individuals Affymetrix, Illumina [up to 2200000] (imputed) 1 symmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006523 GCST002622 Genome-wide genotyping array 2016-06-13 25325441 Baik I 2015-07-01 Sleep www.ncbi.nlm.nih.gov/pubmed/25325441 Associations of Sleep Apnea, NRG1 Polymorphisms, Alcohol Consumption, and Cerebral White Matter Hyperintensities: Analysis with Genome-Wide Association Data. Obstructive sleep apnea 235 Korean ancestry cases, 235 Korean ancestry controls NA Affymetrix [319517] (imputed) 2 obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0003918 GCST003012 Genome-wide genotyping array 2014-11-12 24785509 Barnett GC 2014-04-28 Radiother Oncol www.ncbi.nlm.nih.gov/pubmed/24785509 A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity. Response to radiotherapy in cancer (late toxicity) 579 European ancestry prostate cancer cases, 1,194 European ancestry breast cancer cases 516 European ancestry prostate cancer cases, 862 prostate cancer cases, 355 breast cancer cases Illumina [2417493] (imputed) 10 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002431 Genome-wide genotyping array 2014-04-15 24162738 Hu Z 2013-10-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24162738 New loci associated with chronic hepatitis B virus infection in Han Chinese. Hepatitis B 951 Han Chinese ancestry HBV carrier cases, 937 Han Chinese ancestry HBV cleared controls 4,230 Chinese ancestry HBV carrier cases, 3,051 Chinese ancestry HBV cleared controls, 2,622 Chinese ancestry controls Illumina [490610] 3 hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004197 GCST002246 Genome-wide genotyping array 2015-05-23 25281661 Matsuda K 2014-10-03 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25281661 Genome-wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population. Bladder cancer 531 Japanese ancestry cases, 5,581 Japanese ancestry conrols 592 Japanese ancestry cases, 6,964 Japanese ancestry controls, 3,508 European ancestry cases, 5,101 European ancestry controls Illumina [554389] 1 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST002645 Genome-wide genotyping array 2014-10-21 24511991 Hill-Burns EM 2014-02-10 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/24511991 Identification of a novel Parkinson's disease locus via stratified genome-wide association study. Parkinson's disease 1,565 European ancestry sproadic Parkinson's disease cases, 435 European ancestry familial Parkinson's disease cases, 1,986 European ancestry controls 1,528 European ancestry sporadic Parkinson's disease cases, 707 European ancestry familial Parkinson's disease cases, 796 European ancestry controls Illumina [811597] 8 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST002353 Genome-wide genotyping array 2015-07-09 25101718 Lee JH 2015-03-01 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/25101718 IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease. Pulmonary artery enlargement and chronic obstructive pulmonary disease 1,006 European ancestry cases, 260 African American cases, 2,712 European ancestry smoker controls, 1,749 African American smoker controls NA Illumina [NR] (imputed) 1 pulmonary artery enlargement, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0006347, http://www.ebi.ac.uk/efo/EFO_0000341 GCST002798 Genome-wide genotyping array 2015-07-09 25101718 Lee JH 2015-03-01 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/25101718 IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease. Pulmonary artery enlargement in chronic obstructive pulmonary disease 1,006 European ancestry cases, 260 African American cases, 3,281 European ancestry controls, 494 African American controls NA Illumina [NR] (imputed) 2 pulmonary artery enlargement http://www.ebi.ac.uk/efo/EFO_0006347 GCST002797 Genome-wide genotyping array 2015-07-09 25101718 Lee JH 2015-03-01 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/25101718 IREB2 and GALC are associated with pulmonary artery enlargement in chronic obstructive pulmonary disease. Chronic obstructive pulmonary disease 3,281 European ancestry cases, 494 African American cases, 2,712 European ancestry smoker controls, 1,749 African American smoker controls NA Illumina [NR] (imputed) 5 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST002795 Genome-wide genotyping array 2014-12-03 24871321 Sambo F 2014-05-29 Diabetologia www.ncbi.nlm.nih.gov/pubmed/24871321 Novel genetic susceptibility loci for diabetic end-stage renal disease identified through robust naive Bayes classification. End-stage renal disease or diabetic nephropathy in type 1 diabetes 661 European ancestry End-stage renal disease cases, 694 European ancestry Diabetic nephropathy cases, 472 European ancestry Microalbuminuria cases, 1,637 European ancestry controls 92 End-stage renal disease cases, 345 Diabetic nephropathy cases, 135 Microalbuminuria cases, 370 controls Illumina [549530] 0 chronic kidney disease, diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0000401 GCST002464 Genome-wide genotyping array 2015-04-24 25187374 Hwang JY 2014-09-03 Diabetes www.ncbi.nlm.nih.gov/pubmed/25187374 Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. Fasting plasma glucose 24,740 East Asian ancestry individuals 21,345 East Asian ancestry individuals Affymetrix, Illumina [up to 2315813] (imputed) 14 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST002586 Genome-wide genotyping array 2015-04-30 25173105 Gharahkhani P 2014-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25173105 Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma. Glaucoma (primary open-angle) 1,155 European ancestry cases, 1,922 European ancestry controls 3,548 European ancestry cases, 9,496 European ancestry controls Illumina [7594768] (imputed) 9 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST002582 Genome-wide genotyping array 2015-07-09 25199915 Broer L 2014-09-08 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/25199915 GWAS of longevity in CHARGE consortium confirms APOE and FOXO3 candidacy. Longevity (90 years and older) 6,036 European ancestry cases, 3,757 European ancestry controls NA Affymetrix, Illumina [2500000] (imputed) 7 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST002599 Genome-wide genotyping array 2014-08-02 24347629 Shaffer JR 2013-12-17 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/24347629 Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years. Periodontal disease-related phenotype (Socransky) 93 European ancestry cases, 83 European ancestry individuals, 497 European ancestry controls NA Illumina [~ 1400000] (imputed) 10 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST002312 Genome-wide genotyping array 2008-07-22 17658951 Scuteri A 2007-07-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/17658951 Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. Obesity-related traits 4,741 Sardinian individuals 3,205 African American, Hispanic, and European ancestry individuals Affymetrix [362129] 3 body weight, waist-hip ratio, body mass index http://www.ebi.ac.uk/efo/EFO_0004338, http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004340 GCST000060 Genome-wide genotyping array 2014-10-23 24667120 Zhang TX 2014-03-25 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24667120 Genome-wide association study identifies new disease loci for isolated clubfoot. Clubfoot 396 European ancestry cases, 1,000 European ancestry controls 370 European ancestry cases, 363 European ancestry controls Affymetrix [620820] (imputed) 1 familial clubfoot with or without associated lower limb anomalies http://purl.obolibrary.org/obo/MONDO_0016046 GCST002399 Genome-wide genotyping array 2014-08-05 24351856 Nanayakkara S 2013-12-18 J Occup Health www.ncbi.nlm.nih.gov/pubmed/24351856 An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka. Chronic kidney disease 301 Sri Lankan Sinhalese ancestry cases, 276 Sri Lankan Sinhalese ancestry controls NA Illumina [543848] 1 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST002313 Genome-wide genotyping array 2014-08-02 24351856 Nanayakkara S 2013-12-18 J Occup Health www.ncbi.nlm.nih.gov/pubmed/24351856 An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka. Glomerular filtration rate 301 Sri Lankan Sinhalese ancestry cases, 276 Sri Lankan Sinhalese ancestry controls NA Illumina [543848] 4 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST002314 Genome-wide genotyping array 2015-07-07 25409777 Thyagarajan B 2014-11-01 Respir Res www.ncbi.nlm.nih.gov/pubmed/25409777 Genetic variants associated with lung function: the long life family study. Pulmonary function 3,889 European ancestry individuals 48,201 individuals Illumina [6522421] (imputed) 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST002683 Genome-wide genotyping array 2014-12-10 24892410 Leu HB 2014-06-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/24892410 A novel SNP associated with nighttime pulse pressure in young-onset hypertension patients could be a genetic prognostic factor for cardiovascular events in a general cohort in Taiwan. Pulse pressure in young-onset hypertension 382 individuals 559 individuals Illumina [560186] 1 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST002470 Genome-wide genotyping array 2011-12-14 22065538 Morisaki H 2011-11-07 Hum Mutat www.ncbi.nlm.nih.gov/pubmed/22065538 CDH13 gene coding T-cadherin influences variations in plasma adiponectin levels in the Japanese population. Adiponectin levels 3,310 Japanese ancestry individuals NA Illumina [348622] 1 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST001314 Genome-wide genotyping array 2015-07-07 25233373 Simpson CL 2014-09-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25233373 Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. Hyperopia 7,068 European ancestry cases, 6,844 European ancestry controls 1,554 European ancestry cases, 892 cases, 1,654 European ancestry controls, 2,921 controls Affymetrix, Illumina [up to 3397980] (imputed) 5 Hypermetropia http://purl.obolibrary.org/obo/HP_0000540 GCST002617 Genome-wide genotyping array 2015-07-07 25233373 Simpson CL 2014-09-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25233373 Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. Myopia 3,923 European ancestry cases, 11,696 European ancestry controls 1,410 European ancestry cases, 2,921 cases, 3,171 European ancestry controls, 998 controls Affymetrix, Illumina [up to 3397980] (imputed) 4 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST002615 Genome-wide genotyping array 2015-07-15 25407941 Sleiman PM 2014-11-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25407941 GWAS identifies four novel eosinophilic esophagitis loci. Eosinophilic esophagitis 603 European ancestry cases, 3,637 European ancestry controls 333 European ancestry cases, 675 European ancestry controls Illumina [~ 2300000] (imputed) 6 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST002697 Genome-wide genotyping array 2015-05-07 25218607 Coleman EA 2014-09-14 Support Care Cancer www.ncbi.nlm.nih.gov/pubmed/25218607 GWAS of 972 autologous stem cell recipients with multiple myeloma identifies 11 genetic variants associated with chemotherapy-induced oral mucositis. Response to chemotherapy in multiple myeloma (oral mucositis) (high-dose melphalan) 619 European ancestry cases with grades 0-1 oral mucositis, 353 European ancestry cases with grades 2-4 oral mucositis NA Illumina [892589] 0 response to high-dose melphalan, chemotherapy-induced oral mucositis http://www.ebi.ac.uk/efo/EFO_0006314, http://www.ebi.ac.uk/efo/EFO_0006313 GCST002605 Genome-wide genotyping array 2015-05-23 25224454 Li J 2014-09-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25224454 Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans. Iron status biomarkers 2,347 African American individuals 329 African American individuals Affymetrix [~ 17000000] (imputed) 3 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST002609 Genome-wide genotyping array 2015-05-15 21368711 Alliey-Rodriguez N 2011-03-02 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/21368711 Genome-wide association study of personality traits in bipolar patients. Personality traits in bipolar disorder 1,951 European ancestry cases NA Affymetrix [702866] 7 personality trait http://www.ebi.ac.uk/efo/EFO_0004365 GCST000995 Genome-wide genotyping array 2015-05-07 25256182 Foroud T 2014-09-25 Stroke www.ncbi.nlm.nih.gov/pubmed/25256182 Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. Intracranial aneurysm 2,617 European ancestry cases, 2,548 European ancestry controls 1,516 European ancestry cases, 5,321 European ancestry controls Affymetrix [685281] (imputed) 4 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST002633 Genome-wide genotyping array 2015-02-06 24962325 Kapoor M 2014-06-11 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/24962325 Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families. Alcohol dependence (age at onset) 685 European ancestry cases, 1,103 European ancestry controls from 118 families NA Illumina [4058415] (imputed) 28 age of onset of alcohol dependence http://purl.obolibrary.org/obo/OBA_2001016 GCST002477 Genome-wide genotyping array 2008-06-16 17460697 Steinthorsdottir V 2007-04-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17460697 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. Type 2 diabetes 1,399 European ancestry cases, 5,275 European ancestry controls 2,174 European ancestry cases, 7,287 European ancestry controls Illumina [at least 313179] 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000027 Genome-wide genotyping array 2010-05-18 20410501 Jin Y 2010-04-21 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/20410501 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. Vitiligo 1,392 European ancestry cases, 2,629 European ancestry controls 647 European ancestry cases, 1,056 European ancestry controls, 183 European ancestry trios, 1,383 European ancestry individuals from 332 families Illumina [520460] 10 Vitiligo http://www.ebi.ac.uk/efo/EFO_0004208 GCST000662 Genome-wide genotyping array 2014-11-19 24852370 Zhan M 2014-05-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24852370 Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations. Serum thyroid-stimulating hormone levels 1,346 Han Chinese ancestry individuals 3,235 She Chinese ancestry individuals Illumina [8503852] (imputed) 4 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST002458 Genome-wide genotyping array 2015-04-01 24986923 Chu M 2014-07-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24986923 A genome-wide association study identifies susceptibility loci of silica-related pneumoconiosis in Han Chinese. Pneumoconiosis in silica exposure 202 Han Chinese ancestry cases, 198 Han Chinese ancestry controls 490 Han Chinese ancestry cases, 541 Han Chinese ancestry controls Illumina [710999] (imputed) 3 response to silica exposure, pneumoconiosis http://www.ebi.ac.uk/efo/EFO_0005853, http://purl.obolibrary.org/obo/MONDO_0015926 GCST002515 Genome-wide genotyping array 2010-12-08 20972438 Rothman N 2010-10-24 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20972438 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. Bladder cancer 3,532 European ancestry cases, 5,120 European ancestry controls 8,381 cases, 48,275 controls Illumina [589299] 10 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST000842 Genome-wide genotyping array 2014-05-01 24101674 Hanson RL 2013-10-07 Diabetes www.ncbi.nlm.nih.gov/pubmed/24101674 A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes. Type 2 diabetes 278 American Indian ancestry young-onset cases, 129 American Indian ancestry cases, 424 American Indian ancestry controls from 514 sibships 1,273 American Indian ancestry cases, 1,635 American Indian ancestry controls, 793 cases, 3,133 controls Affymetrix [453654] 2 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002224 Genome-wide genotyping array 2014-07-20 24249740 Zhang L 2013-11-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24249740 Multistage genome-wide association meta-analyses identified two new loci for bone mineral density. Bone mineral density 5,833 European ancestry females, 2,639 European ancestry males, 784 Han Chinese ancestry females, 763 Han Chinese ancestry males, 712 African American females, 409 Hispanic females 7,010 European ancestry females, 3,772 European ancestry males, 2,980 East Asian ancestry females, 2,159 East Asian ancestry males Affymetrix, Illumina [5842825] (imputed) 24 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST002276 Genome-wide genotyping array 2010-03-17 20167575 Sun Q 2010-02-22 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/20167575 Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels. Soluble leptin receptor levels 684 European ancestry type 2 diabetes female cases, 820 European ancestry female controls 875 European ancestry male individuals Affymetrix [2543887] (imputed) 1 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST000605 Genome-wide genotyping array 2015-09-22 25305756 Kiryluk K 2014-10-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25305756 Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens. IgA nephropathy 1,194 Han Chinese ancestry cases, 902 Han Chinese ancestry controls, 1,553 European ancestry cases, 3,050 European ancestry controls 2,491 East Asian ancestry cases, 1,780 East Asian ancestry controls, 2,420 European ancestry cases, 7,222 European ancestry controls Illumina [> 1000000] (imputed) 32 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST002655 Genome-wide genotyping array 2015-12-04 25584925 Chen W 2015-01-13 Ann Am Thorac Soc www.ncbi.nlm.nih.gov/pubmed/25584925 A genome-wide association study of chronic obstructive pulmonary disease in Hispanics. Chronic obstructive pulmonary disease 94 Costa Rican founder population smoker cases, 412 Costa Rican founder population smoker controls, 63 Hispanic ancestry cases, 619 Hispanic ancestry controls 47 Hispanic ancestry smoker cases, 290 Hispanic ancestry smoker controls Affymetrix, Illumina [~ 2600000] (imputed) 3 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST002750 Genome-wide genotyping array 2014-07-29 24315451 van der Valk RJ 2013-12-05 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/24315451 Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants. Fractional exhaled nitric oxide (childhood) 5,131 European ancestry individuals, 1,155 Hispanic individuals, 2,572 individuals NA Affymetrix, Illumina [2253077] (imputed) 25 nitric oxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0005536 GCST002304 Genome-wide genotyping array 2014-10-10 24413707 Chiang KM 2014-01-11 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/24413707 A three-stage genome-wide association study combining multilocus test and gene expression analysis for young-onset hypertension in Taiwan Han Chinese. Hypertension (young onset) 400 Han Chinese ancestry cases, 400 Han Chinese ancestry controls 592 Han Chinese ancestry cases, 592 Han Chinese ancestry controls, 315 Han Chinese ancestry individuals from 111 families, 1,999 European ancestry cases, 3,004 European ancestry controls Illumina [497849] 0 early onset hypertension http://www.ebi.ac.uk/efo/EFO_0004772 GCST002332 Genome-wide genotyping array 2013-02-20 23212062 Fanous AH 2012-12-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/23212062 Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms. Schizophrenia 2,454 European ancestry cases NA Affymetrix [696491] 16 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST001757 Genome-wide genotyping array 2011-04-04 21379329 Wijsman EM 2011-02-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21379329 Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. Alzheimer's disease (late onset) 1,848 European ancestry affected individuals, 1,991 European ancestry unaffected individuals 231 Caribbean Hispanic cases, 187 Caribbean Hispanic controls, 386 European ancestry cases, 386 European ancestry controls Illumina [565336] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000980 Genome-wide genotyping array 2012-10-13 22864923 Yang C 2012-08-03 Immunogenetics www.ncbi.nlm.nih.gov/pubmed/22864923 Genome-wide association study identifies TNFSF13 as a susceptibility gene for IgA in a South Chinese population in smokers. IgA levels 1,999 Han Chinese ancestry male individuals 1,496 East Asian ancestry male individuals Illumina [1940243] (imputed) 1 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST001626 Genome-wide genotyping array 2013-01-15 23225573 Buck D 2012-09-08 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/23225573 Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis. IgG levels 229 European ancestry multiple sclerosis cases 409 European ancestry multiple sclerosis cases Illumina [526014] 1 serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0004565 GCST001671 Genome-wide genotyping array 2012-03-27 22391508 Jiang R 2012-03-05 Environ Health Perspect www.ncbi.nlm.nih.gov/pubmed/22391508 Single-nucleotide polymorphisms associated with skin naphthyl-keratin adduct levels in workers exposed to naphthalene. Naphthyl-keratin adduct levels 100 European, Hispanic, African American and Asian ancestry individuals NA Affymetrix [184153] 0 naphthyl-keratin adduct measurement http://www.ebi.ac.uk/efo/EFO_0004585 GCST001434 Genome-wide genotyping array 2013-02-21 23273568 Yang W 2012-12-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23273568 Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. Systemic lupus erythematosus 1,656 Han Chinese ancestry cases, 3,394 Han Chinese ancestry controls 3,256 Han Chinese ancestry cases, 5,667 Han Chinese ancestry controls, 453 Thai ancestry cases, 963 Thai ancestry controls Illumina [2100739] (imputed) 34 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST001795 Genome-wide genotyping array 2014-11-15 24797007 Holliday EG 2014-05-01 Am J Gastroenterol www.ncbi.nlm.nih.gov/pubmed/24797007 Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome. Irritable bowel syndrome Up to 172 European ancestry cases, 1,398 European ancestry controls Up to 485 European ancestry cases, up to 716 European ancestry controls Affymetrix [~ 2500000] (imputed) 2 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST002436 Genome-wide genotyping array 2012-11-22 22899653 Timofeeva MN 2012-08-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22899653 Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls. Lung cancer up to 14,900 European ancestry cases, up to 29,485 European ancestry controls 2,338 Han Chinese ancestry cases, 3,077 Han Chinese ancestry controls Illumina [up to 536008] 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST001638 Genome-wide genotyping array 2014-02-10 21964575 Rafnar T 2011-10-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21964575 Mutations in BRIP1 confer high risk of ovarian cancer. Ovarian cancer 640 European ancestry cases, 41,607 European ancestry controls NA Illumina [15957390] (imputed) 1 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST001258 Genome-wide genotyping array 2014-04-02 24080446 Rudolph A 2013-11-04 Endocr Relat Cancer www.ncbi.nlm.nih.gov/pubmed/24080446 Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study. Breast cancer (menopausal hormone therapy interaction) 2,920 European ancestry cases 7,689 European ancestry cases, 9,266 European ancestry controls Illumina [2500000] (imputed) 2 breast carcinoma, hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0003961 GCST002265 Genome-wide genotyping array 2014-04-02 24080446 Rudolph A 2013-11-04 Endocr Relat Cancer www.ncbi.nlm.nih.gov/pubmed/24080446 Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study. Lobular breast cancer (menopausal hormone therapy interaction) 541 European ancestry cases 676 European ancestry cases, 9,266 European ancestry controls Illumina [2500000] (imputed) 2 invasive lobular carcinoma, hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0000553, http://www.ebi.ac.uk/efo/EFO_0003961 GCST002266 Genome-wide genotyping array 2011-01-06 21068099 Evangelou E 2010-11-10 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/21068099 Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22. Osteoarthritis 2,371 European ancestry cases, 35,909 European ancestry controls 4,338 European ancestry cases, 8,530 European ancestry controls, 1,183 East Asian ancestry cases, 1,245 East Asian ancestry controls Affymetrix, Illumina [2335627] (imputed) 1 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST000869 Genome-wide genotyping array 2013-02-20 23213074 Adams LA 2012-12-05 Hepatology www.ncbi.nlm.nih.gov/pubmed/23213074 Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease. Non-alcoholic fatty liver disease histology (other) 126 European ancestry adolescent cases, 802 European ancestry adolescent controls NA Illumina [2078805] (imputed) 4 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST001766 Genome-wide genotyping array 2014-03-19 23974705 Allen EK 2013-08-23 J Assoc Res Otolaryngol www.ncbi.nlm.nih.gov/pubmed/23974705 A genome-wide association study of chronic otitis media with effusion and recurrent otitis media identifies a novel susceptibility locus on chromosome 2. Otitis media (chronic/recurrent) 373 cases and 229 controls from 143 families 932 European ancestry cases and 652 European ancestry controls from 441 families Illumina [324748] 1 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST002148 Genome-wide genotyping array 2014-08-01 17903308 Gottlieb DJ 2007-09-19 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/17903308 Genome-wide association of sleep and circadian phenotypes. Sleep-related phenotypes up to 738 individuals from 203 families NA Affymetrix [70897] 5 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST000081 Genome-wide genotyping array 2014-06-19 24292274 Speedy HE 2013-12-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24292274 A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia. Chronic lymphocytic leukemia 1,739 European ancestry cases, 5,199 European ancestry controls 1,144 European ancestry cases, 3,151 European ancestry controls Illumina [450000] (imputed) 19 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST002299 Genome-wide genotyping array 2014-03-13 23955597 Chubb D 2013-08-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23955597 Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk. Multiple myeloma 2,335 European ancestry cases, 7,306 European ancestry controls 2,357 European ancestry cases, 3,684 European ancestry controls Illumina [414804] 6 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST002140 Genome-wide genotyping array 2014-12-11 24916648 Hirokawa M 2014-06-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24916648 A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese. Myocardial infarction 1,666 Japanese ancestry cases, 3,198 Japanese ancestry controls 11,412 Japanese ancestry cases, 28,397 Japanese ancestry controls Illumina [455781] 4 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST002475 Genome-wide genotyping array 2014-02-13 21983786 Sulem P 2011-10-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21983786 Identification of low-frequency variants associated with gout and serum uric acid levels. Gout 968 European ancestry cases, 40,000 European ancestry controls NA Illumina [15957390] (imputed) 3 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST001268 Genome-wide genotyping array 2014-02-13 21983786 Sulem P 2011-10-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21983786 Identification of low-frequency variants associated with gout and serum uric acid levels. Serum uric acid levels 15,506 European ancestry individuals NA Illumina [15957390] (imputed) 5 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST001269 Genome-wide genotyping array 2010-02-04 20062060 Pfeufer A 2010-01-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20062060 Genome-wide association study of PR interval. PR interval 28,517 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 9 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST000562 Genome-wide genotyping array 2017-08-02 25065397 Gialluisi A 2014-07-28 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/25065397 Genome-wide screening for DNA variants associated with reading and language traits. Reading disability or specific language impairment (pleiotropy) 548 children from 288 families, 749 children from 343 unrelated twinships/sibliships, 959 children NA Illumina [at least 6190549] (imputed) 8 specific language impairment, dyslexia http://www.ebi.ac.uk/efo/EFO_1001510, http://www.ebi.ac.uk/efo/EFO_0005424 GCST004401 Genome-wide genotyping array 2017-08-02 25065397 Gialluisi A 2014-07-28 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/25065397 Genome-wide screening for DNA variants associated with reading and language traits. Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) 1,826 children NA Illumina [at least 6190549] (imputed) 5 intelligence, specific language impairment, dyslexia http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_1001510, http://www.ebi.ac.uk/efo/EFO_0005424 GCST004402 Genome-wide genotyping array 2015-06-07 25328121 Lee JY 2014-10-17 J Atheroscler Thromb www.ncbi.nlm.nih.gov/pubmed/25328121 Associations between Genetic Variants and Angiographic Characteristics in Patients with Coronary Artery Disease. Coronary artery disease-related phenotypes 667 Korean ancestry cases 853 Korean ancestry cases Affymetrix [542675] 0 angiographic measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0006512, http://www.ebi.ac.uk/efo/EFO_0001645 GCST002659 Genome-wide genotyping array 2015-01-20 24963161 Chen P 2014-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24963161 CMPK1 and RBP3 are associated with corneal curvature in Asian populations. Corneal curvature 3,178 Chinese ancestry individuals, 2,138 Malay ancestry individuals, 2,124 Asian Indian ancestry individuals 2,473 Chinese ancestry individuals, 2,747 Japanese ancestry individuals Illumina [~ 7000000] (imputed) 4 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST002502 Genome-wide genotyping array 2013-01-16 23049088 Meng W 2012-10-09 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/23049088 A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. Myopia (pathological) 187 European ancestry cases, 1064 European ancestry controls Affymetrix, Illumina [152234] 64 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST001712 Genome-wide genotyping array 2014-04-09 24132900 Kanazawa T 2013-10-01 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/24132900 Genome-wide association study of atypical psychosis. Psychosis (atypical) 47 Japanese ancestry cases, 882 Japanese ancestry controls NA Affymetrix [545513] 10 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST002211 Genome-wide genotyping array 2014-07-29 24348519 Namjou B 2013-12-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/24348519 EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. Body mass index up to 2,860 European ancestry children NA Affymetrix, Illumina [up to 583824] (imputed) 8 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002301 Genome-wide genotyping array 2013-02-06 23183491 Nishizawa D 2012-11-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23183491 Genome-wide association study identifies a potent locus associated with human opioid sensitivity. Opioid sensitivity 118 Japanese ancestry individuals 235 Japanese ancestry individuals Illumina [295036] 1 response to isoquinoline alkaloid http://purl.obolibrary.org/obo/GO_0014072 GCST001751 Genome-wide genotyping array 2014-11-14 24801482 Baron-Cohen S 2014-05-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/24801482 A genome wide association study of mathematical ability reveals an association at chromosome 3q29, a locus associated with autism and learning difficulties: a preliminary study. Mathematical ability 419 European ancestry individuals with high mathematical ability, 183 European ancestry individuals with low mathematical ability NA Affymetrix [906600] 0 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST002439 Genome-wide genotyping array 2014-03-23 24037343 Chang ALS 2013-09-13 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/24037343 Identification of genes promoting skin youthfulness by genome-wide association study. Skin youthfulness 218 Ashkenazi Jewish cases, 210 Ashkenazi Jewish controls 408 Ashkenazi Jewish cases, 399 Ashkenazi Jewish controls Affymetrix [901470] 0 skin aging http://www.ebi.ac.uk/efo/EFO_0005422 GCST002189 Genome-wide genotyping array 2012-09-29 22869035 Logue MW 2012-08-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/22869035 A genome-wide association study of post-traumatic stress disorder identifies the retinoid-related orphan receptor alpha (RORA) gene as a significant risk locus. Post-traumatic stress disorder 295 European ancestry cases, 196 European ancestry controls 143 African American cases, 462 African American controls Illumina [1199491] 0 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST001630 Genome-wide genotyping array 2009-10-05 19772629 Latourelle JC 2009-09-22 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/19772629 Genomewide association study for onset age in Parkinson disease. Parkinson's disease (age of onset) 857 European ancestry familial cases, 440 idiopathic cases 747 European ancestry idiopathic cases Illumina, Perlegen [1861750] (imputed) 5 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST000490 Genome-wide genotyping array 2014-01-31 20981099 Kong A 2010-10-28 Nature www.ncbi.nlm.nih.gov/pubmed/20981099 Fine-scale recombination rate differences between sexes, populations and individuals. Recombination measurement (females) 6,041 European ancestry female individuals NA Illumina [497256] (imputed) 1 recombination rate http://www.ebi.ac.uk/efo/EFO_0004863 GCST000848 Genome-wide genotyping array 2014-01-31 20981099 Kong A 2010-10-28 Nature www.ncbi.nlm.nih.gov/pubmed/20981099 Fine-scale recombination rate differences between sexes, populations and individuals. Recombination measurement (males) 4,389 European ancestry male individuals NA Illumina [497256] (imputed) 1 recombination rate http://www.ebi.ac.uk/efo/EFO_0004863 GCST000845 Genome-wide genotyping array 2014-05-13 24204295 Han F 2013-10-31 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24204295 Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. Narcolepsy 1,189 Chinese ancestry cases, 1,997 Chinese ancestry controls 2,693 European ancestry cases, 11,495 European ancestry controls Affymetrix [603382] 5 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST002260 Genome-wide genotyping array 2014-05-13 24204295 Han F 2013-10-31 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24204295 Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. Narcolepsy (onset before 2009 H1N1 influenza pandemic) up to 893 Chinese ancestry cases with onset before the 2009 H1N1 influenza pandemic, up to 373 Chinese ancestry cases with onset after the 2009 H1N1 influenza pandemic NA Affymetrix [603382] 2 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST002259 Genome-wide genotyping array 2014-05-13 24204295 Han F 2013-10-31 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24204295 Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic. Narcolepsy (age of onset) at least 1,000 Chinese ancestry cases NA Affymetrix [603382] 3 age of onset of narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/OBA_2001032 GCST002261 Genome-wide genotyping array 2014-12-11 24908248 Walsh KM 2014-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24908248 Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk. Glioma (high-grade) 1,013 European ancestry cases, 6,595 European ancestry controls 631 European ancestry cases, 1,141 European ancestry controls Affymetrix, Illumina [2362330] (imputed) 3 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST002474 Genome-wide genotyping array 2015-05-11 25055868 Sano M 2014-07-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25055868 Genome-wide association study of electrocardiographic parameters identifies a new association for PR interval and confirms previously reported associations. Electrocardiographic traits 2,994 Japanese ancestry individuals 6,805 Korean ancestry individuals Illumina [~ 2500000] 9 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST002542 Genome-wide genotyping array 2013-03-05 23181788 Lasky-Su J 2012-12-04 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/23181788 HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults. Asthma Up to 1,238 European ancestry cases, up to 2,617 European ancestry controls Up to 1,837 European ancestry cases, up to 3,803 European ancestry controls, up to 2,806 cases, up to 2,150 controls, up to 603 Costa Rican ancestry cases and their parents Affymetrix [455089] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001763 Genome-wide genotyping array 2014-12-16 24934506 Eny KM 2014-06-17 Diabetologia www.ncbi.nlm.nih.gov/pubmed/24934506 GWAS identifies an NAT2 acetylator status tag single nucleotide polymorphism to be a major locus for skin fluorescence. Skin fluorescence 1,082 European ancestry individuals with type 1 diabetes, 8,721 European ancestry individuals 202 European ancestry individuals with type 1 diabetes, 318 European ancestry individuals with type 2 diabetes, 515 European ancestry individuals Illumina [up to 1609583] (imputed) 0 skin fluorescence measurement http://www.ebi.ac.uk/efo/EFO_0005766 GCST002484 Genome-wide genotyping array 2008-06-27 18519826 Uhl GR 2008-06-04 Arch Gen Psychiatry www.ncbi.nlm.nih.gov/pubmed/18519826 Molecular genetics of successful smoking cessation: convergent genome-wide association study results. Smoking cessation 241 European ancestry successful abstainers, 309 European ancestry unsuccessful abstainers NA Affymetrix [~ 500000] 0 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST000203 Genome-wide genotyping array 2015-09-22 25551457 Baumert J 2014-12-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/25551457 No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects. Fibrinogen levels (smoking status, alcohol consumption or body mass index interaction) up to 80,607 European ancestry individuals NA Affymetrix, Illumina [~ 2600000] (imputed) 3 smoking status measurement, alcohol drinking, fibrinogen measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004329, http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0004340 GCST002734 Genome-wide genotyping array 2014-02-05 23836780 Blue Mountains Eye Study (BMES) 2013-07-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23836780 Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus. Intraocular pressure 2,175 European ancestry individuals 4,866 European ancestry individuals Illumina [6235970] 1 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST002089 Genome-wide genotyping array 2015-09-22 25517131 Dijkstra AE 2015-02-27 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/25517131 Novel genes for airway wall thickness identified with combined genome-wide association and expression analyses. Airway wall thickness 2,640 individuals up to 714 individuals Illumina [522636] 19 airway wall thickness measurement http://www.ebi.ac.uk/efo/EFO_0006898 GCST002794 Genome-wide genotyping array 2014-04-11 24133439 Jones RM 2013-10-11 Front Hum Neurosci www.ncbi.nlm.nih.gov/pubmed/24133439 Genome-wide association study of autistic-like traits in a general population study of young adults. Social autistic-like traits 965 European ancestry young adult individuals NA Illumina [2462046] (imputed) 6 autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0005426 GCST002228 Genome-wide genotyping array 2015-09-19 25557950 Alonso A 2014-12-31 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/25557950 Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study. Crohn's disease-related phenotypes up to 1,090 Southern European ancestry Crohn's disease cases up to 1,296 Southern European ancestry Crohn's disease cases Illumina [539846] 7 stricture, ileocolitis, perianal Crohn's disease, Erythema nodosum, Crohn's disease, mild disease course, complicated disease course http://www.ebi.ac.uk/efo/EFO_0006818, http://www.ebi.ac.uk/efo/EFO_0005624, http://www.ebi.ac.uk/efo/EFO_0005627, http://purl.obolibrary.org/obo/HP_0012219, http://www.ebi.ac.uk/efo/EFO_0000384, http://www.ebi.ac.uk/efo/EFO_0006819, http://www.ebi.ac.uk/efo/EFO_0006820 GCST002729 Genome-wide genotyping array 2014-06-25 24190013 Earp MA 2013-11-05 Hum Genet www.ncbi.nlm.nih.gov/pubmed/24190013 Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA. Epithelial ovarian cancer 84 European ancestry mucinous cases, 114 European ancestry endometroid or clear cell cases, 75 European ancestry low malignant potential serous cases, 272 European ancestry invasive serous cases, 398 European ancestry controls 1,483 European ancestry mucinous cases, 2,903 European ancestry endometroid or clear cell cases, 892 European ancestry low malignant potential serous cases, 6,881 European ancestry invasive serous cases, up to 21,530 European ancestry controls Illumina [up to 448500] 0 malignant epithelial tumor of ovary http://purl.obolibrary.org/obo/MONDO_0018364 GCST002267 Genome-wide genotyping array 2014-03-20 23958962 Gelernter J 2013-08-20 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23958962 Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. Cocaine dependence 1,809 European ancestry cases, 570 European ancestry controls, 2,482 African American cases, 836 African American controls 4,498 European ancestry individuals, 2,114 African American individuals Illumina [37426733] (imputed) 15 cocaine dependence http://www.ebi.ac.uk/efo/EFO_0002610 GCST002142 Genome-wide genotyping array 2012-12-21 23049750 Kumasaka N 2012-09-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/23049750 Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population. Smoking behavior 11,696 Japanese ancestry smokers 5,462 Japanese ancestry smokers Illumina [2312503] (imputed) 3 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST001696 Genome-wide genotyping array 2013-02-19 23229837 Aragam N 2012-12-11 J Mol Neurosci www.ncbi.nlm.nih.gov/pubmed/23229837 TMPRSS9 and GRIN2B are associated with neuroticism: a genome-wide association study in a European sample. Neuroticism 2,748 European ancestry cases NA Perlegen [437547] 1 neurotic disorder http://www.ebi.ac.uk/efo/EFO_0004257 GCST001771 Genome-wide genotyping array 2014-08-02 24388013 Ferreira MA 2013-12-30 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/24388013 Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. Asthma and hay fever 6,685 European ancestry cases, 14,091 European ancestry controls 878 European ancestry cases, 2,455 European ancestry controls Illumina [up to 4972397] (imputed) 21 asthma, seasonal allergic rhinitis http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0003956 GCST002322 Genome-wide genotyping array 2008-06-16 17618283 Zanke BW 2007-07-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17618283 Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. Colorectal cancer 1,257 cases, 1,336 controls 5,084 European ancestry cases, 5,388 European ancestry controls, 1,139 cases, 1,055 controls Affymetrix, Illumina [99632] 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000052 Genome-wide genotyping array 2015-04-01 25027320 Ramirez A 2014-07-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25027320 SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease. Cerebrospinal AB1-42 levels in Alzheimer's disease dementia 363 European ancestry individuals 515 individuals Illumina [6812394] (imputed) 2 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST002531 Genome-wide genotyping array 2014-06-21 24282030 Pan L 2013-11-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24282030 A genome-wide association study identifies polymorphisms in the HLA-DR region associated with non-response to hepatitis B vaccination in Chinese Han populations. Hepatitis B vaccine response 108 Han Chinese ancestry high-responder cases, 77 Han Chinese ancestry non-responder controls 1,336 Han Chinese ancestry high-responder cases, 420 Han Chinese ancestry non-responder controls Illumina [588026] 2 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST002297 Genome-wide genotyping array 2013-12-12 23817570 Shi Y 2013-06-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23817570 A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12. Cervical cancer Up to 1,364 Han Chinese ancestry cases, up to 3,028 Han Chinese ancestry controls 4,167 Han Chinese ancestry cases, 7,196 Han Chinese ancestry controls Affymetrix [563339] 4 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST002082 Genome-wide genotyping array 2011-07-19 21708048 Jiao H 2011-06-28 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/21708048 Genome wide association study identifies KCNMA1 contributing to human obesity. Obesity 164 European ancestry morbidly obese individuals, 163 European ancestry lean individuals 4,674 European ancestry morbidly obese individuals, 5,663 European ancestry lean individuals Affymetrix [406177] 2 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST001130 Genome-wide genotyping array 2013-01-11 23104006 Nyholt DR 2012-10-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23104006 Genome-wide association meta-analysis identifies new endometriosis risk loci. Endometriosis 3,181 European ancestry cases, 8,075 European ancestry controls, 1,423 Japanese ancestry cases, 1,318 Japanese ancestry controls 1,044 Japanese ancestry, 4,017 Japanese ancestry controls Illumina [407632] 7 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST001720 Genome-wide genotyping array 2014-03-13 23966204 Ledda M 2013-08-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23966204 GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics. Bitter taste perception 503 Brazilian ancestry individuals 104 Brazilian ancestry individuals Illumina [~ 1000000] 3 sensory perception of bitter taste http://purl.obolibrary.org/obo/GO_0050913 GCST002144 Genome-wide genotyping array 2013-01-15 23108145 Wang LE 2012-10-29 Cancer Res www.ncbi.nlm.nih.gov/pubmed/23108145 Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer. Lung Cancer (DNA repair capacity) 914 European ancestry non-small cell lung cancer cases, 860 European ancestry controls 679 European ancestry ancestry non-small cell lung cancer cases, 695 European ancestry controls Illumina [303669] 2 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST001721 Genome-wide genotyping array 2015-04-15 21775986 Hinch AG 2011-07-20 Nature www.ncbi.nlm.nih.gov/pubmed/21775986 The landscape of recombination in African Americans. Recombination measurement 30,033 African American individuals NA Affymetrix, Illumina [3058149] (imputed) 5 recombination measurement http://www.ebi.ac.uk/efo/EFO_0005919 GCST001168 Genome-wide genotyping array 2011-07-29 21725309 Miki D 2011-07-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21725309 Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers. Chronic hepatitis C infection 212 Japanese ancestry chronic hepatitis C with hepatocellular carcinoma cases, 765 Japanese ancestry chronic hepatitis C without hepatocellular carcinoma cases 710 Japanese ancestry chronic hepatitis C with hepatocellular carcinoma cases, 1,625 Japanese ancestry chronic hepatitis C without hepatocellular carcinoma cases Illumina [467538] 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST001139 Genome-wide genotyping array 2014-02-25 23921680 Kim DS 2013-07-31 Int Arch Allergy Immunol www.ncbi.nlm.nih.gov/pubmed/23921680 A genome-wide association study in Koreans identifies susceptibility loci for allergic nickel dermatitis. Allergic dermatitis (nickel) up to 24 Korean ancestry cases, 52 Korean ancestry controls NA Affymetrix [NR] 2 contact dermatitis due to nickel http://www.ebi.ac.uk/efo/EFO_0005320 GCST002108 Genome-wide genotyping array 2015-05-07 25217962 Heap GA 2014-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25217962 HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants. Response to thiopurine immunosuppressants in inflammatory bowel disease (pancreatitis) (azathioprine and mercaptopurine) 172 European ancestry cases, 2,035 European ancestry controls 78 European ancestry cases, 472 controls Affymetrix, Illumina [2819700] (imputed) 1 response to thiopurine, thiopurine immunosuppressant-induced pancreatitis http://www.ebi.ac.uk/efo/EFO_0006317, http://www.ebi.ac.uk/efo/EFO_0006315 GCST002607 Genome-wide genotyping array 2012-11-20 22936702 Hofmann S 2012-08-30 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/22936702 Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis. Sarcoidosis 637 European ancestry cases, 1,233 European ancestry controls 3,121 European ancestry cases, 4,284 European ancestry controls Affymetrix [677619] 2 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST001654 Genome-wide genotyping array 2013-06-06 23417110 Tin A 2013-02-16 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23417110 Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin. Beta-2 microglubulin plasma levels 6,728 European ancestry individuals Affymetrix [2500000] (imputed) 16 beta-2 microglobulin measurement http://www.ebi.ac.uk/efo/EFO_0005197 GCST001863 Genome-wide genotyping array 2015-06-18 25410890 Frau F 2014-09-01 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/25410890 Genome-wide association study identifies CAMKID variants involved in blood pressure response to losartan: the SOPHIA study. Response to angiotensin II receptor blocker treatment (losartan) (change in systolic blood pressure levels) 372 European ancestry hypertensive individuals 216 European ancestry hypertensive individuals Illumina [1705664] (imputed) 0 systolic blood pressure, blood pressure, response to losartan http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0006518 GCST002583 Genome-wide genotyping array 2015-09-22 25524241 Richter HE 2014-12-15 J Urol www.ncbi.nlm.nih.gov/pubmed/25524241 Genetic contributions to urgency urinary incontinence in women. Urgency urinary incontinence 1,102 European ancestry cases, 405 European ancestry controls 1,133 European ancestry cases, 371 European ancestry controls Illumina [9077347] (imputed) 6 urgency urinary incontinence http://www.ebi.ac.uk/efo/EFO_0006865 GCST002723 Genome-wide genotyping array 2013-09-24 19936222 Chasman DI 2009-11-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/19936222 Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis. Lipid metabolism phenotypes Up to 17,296 European ancestry female individuals Up to 2,700 individuals, Up to 2,000 European ancestry cardiovascular heart disease cases and controls Illumina [335603] 73 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST000533 Genome-wide genotyping array 2013-03-22 23281178 Hong MG 2013-03-01 Hum Mutat www.ncbi.nlm.nih.gov/pubmed/23281178 A genome-wide assessment of variability in human serum metabolism. Metabolite levels 214 European ancestry prostate cancer cases, 188 European ancestry controls 489 European ancestry prostate cancer cases Affymetrix [333722] 9 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST001882 Genome-wide genotyping array 2014-04-01 24039173 McGrath LM 2013-09-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/24039173 Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia. Functional impairment in major depressive disorder, bipolar disorder and schizophrenia 2,246 European ancestry individuals NA Affymetrix [1633452] (imputed) 5 functional impairment measurement http://www.ebi.ac.uk/efo/EFO_0005412 GCST002188 Genome-wide genotyping array 2011-10-05 21909106 Arakawa S 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909106 Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population. Age-related macular degeneration 827 Japanese ancestry cases, 3,323 Japanese ancestry controls 709 Japanese ancestry cases, 15,571 Japanese ancestry controls Illumina [457489] 2 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST001232 Genome-wide genotyping array 2011-10-06 21909107 LeMaire SA 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909107 Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1. Thoracic aortic aneurysms and dissections 765 European ancestry cases, 874 European ancestry controls 548 European ancestry cases, 626 European ancestry controls Illumina [NR] (imputed) 1 thoracic aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0004282 GCST001229 Genome-wide genotyping array 2012-12-21 23056639 de Boer RA 2012-10-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/23056639 A genome-wide association study of circulating galectin-3. Protein biomarker 3,776 European ancestry individuals 3,516 individuals Illumina [2269099] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST001711 Genome-wide genotyping array 2014-11-06 24740207 Moy KA 2014-04-16 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/24740207 Genome-wide association study of circulating vitamin D-binding protein. Serum vitamin D-binding protein levels 1,380 European ancestry males NA Illumina [591610] 3 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST002414 Genome-wide genotyping array 2012-11-12 20173735 Fellay J 2010-02-21 Nature www.ncbi.nlm.nih.gov/pubmed/20173735 ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C. Chronic hepatitis C infection 988 European ancestry cases, 198 African American cases, 100 Hispanic cases NA Illumina [565759] 2 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST000604 Genome-wide genotyping array 2014-10-01 24387323 Kim WJ 2014-01-06 Respirology www.ncbi.nlm.nih.gov/pubmed/24387323 Genome-wide association studies identify locus on 6p21 influencing lung function in the Korean population. Lung function 6,223 Korean ancestry individuals 2,720 Korean ancestry individuals Affymetrix [352228] 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST002328 Genome-wide genotyping array 2014-02-21 23933737 Khor CC 2013-08-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23933737 Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia. Myopia (severe) 1,603 East Asian ancestry cases, 3,427 East Asian ancestry controls 1,241 East Asian ancestry cases, 3,559 East Asian ancestry controls Illumina [250531] 2 pathological myopia http://www.ebi.ac.uk/efo/EFO_0004207 GCST002117 Genome-wide genotyping array 2014-03-05 23903073 Kim HN 2013-08-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23903073 Genome-wide association study of the five-factor model of personality in young Korean women. Personality dimensions 1,089 Korean ancestry females 2,090 Korean ancestry individuals Illumina [2053685] (imputed) 8 personality trait http://www.ebi.ac.uk/efo/EFO_0004365 GCST002111 Genome-wide genotyping array 2014-04-01 24065183 Armour JA 2013-09-25 Heredity (Edinb) www.ncbi.nlm.nih.gov/pubmed/24065183 Genome-wide association study of handedness excludes simple genetic models. Handedness 263 European ancestry left-handed individuals, 2,092 European ancestry right-handed individuals NA Illumina [2535688] (imputed) 1 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST002205 Genome-wide genotyping array 2014-04-01 24065183 Armour JA 2013-09-25 Heredity (Edinb) www.ncbi.nlm.nih.gov/pubmed/24065183 Genome-wide association study of handedness excludes simple genetic models. Handedness 173 European ancestry left-handed individuals, 1,412 European ancestry right-handed individuals NA Illumina [2499296] (imputed) 1 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST002206 Genome-wide genotyping array 2014-05-02 24159190 Seppala I 2013-10-24 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/24159190 Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. Asymmetrical dimethylarginine levels 5110 European ancestry individuals NA Affymetrix, Illumina [10085758] (imputed) 21 asymmetrical dimethylarginine measurement, serum dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006522, http://www.ebi.ac.uk/efo/EFO_0005418 GCST002241 Genome-wide genotyping array 2014-05-02 24159190 Seppala I 2013-10-24 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/24159190 Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. Symmetrical dimethylarginine levels 5110 European ancestry individuals NA Affymetrix, Illumina [10085758] (imputed) 30 serum dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0005418 GCST002239 Genome-wide genotyping array 2014-05-02 24159190 Seppala I 2013-10-24 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/24159190 Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality. Serum dimethylarginine levels (asymmetric/symetric ratio) 5110 European ancestry individuals NA Affymetrix, Illumina [10085758] (imputed) 24 serum dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0005418 GCST002242 Genome-wide genotyping array 2014-01-08 23817571 Bonnelykke K 2013-06-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23817571 Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization. Allergic sensitization 5,789 European ancestry cases, 10,056 European ancestry controls 6,114 European ancestry cases, 9,920 European ancestry controls Affymetrix, Illumina [~ 2500000] (imputed) 12 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST002084 Genome-wide genotyping array 2013-12-16 23743675 Kapoor M 2013-06-07 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23743675 A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. Alcohol consumption 2,322 European ancestry individuals from 118 families, 2,593 European ancestry individuals Illumina [4058415] (imputed) 16 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST002065 Genome-wide genotyping array 2015-04-03 25087078 Anney RJ 2014-07-30 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/25087078 Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies. Epilepsy 405 European ancestry cases, 127 African American cases, 248 cases, 2,330 European ancestry genetic generalised epilepsy cases, 81 African American genetic generalised epilepsy cases, 195 genetic generalised epilepsy cases, 3,277 European ancestry focal epilepsy cases, 222 African American focal epilepsy cases, 487 Han Chinese ancestry focal epilepsy cases, 1,324 focal epilepsy cases, up to 17,441 European ancestry controls, up to 2,843 African American controls, up to 2,875 Han Chinese ancestry controls, up to 2,998 controls NA Affymetrix, Illumina [NR] (imputed) 9 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST002547 Genome-wide genotyping array 2015-07-08 25086665 Wolpin BM 2014-08-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25086665 Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer. Pancreatic cancer 1,582 European ancestry cases, 5,203 European ancestry controls 6,101 European ancestry cases, 9,194 European ancestry controls Illumina [608202] 10 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST002553 Genome-wide genotyping array 2014-11-27 24861553 Wen W 2014-05-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24861553 Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. Body mass index 82,438 East Asian ancestry individuals, 4,301 South East Asian ancestry individuals Up to 47,352 East Asian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 25 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002461 Genome-wide genotyping array 2013-01-18 23103227 Jin G 2012-10-25 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23103227 Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese. Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) 2,331 Han Chinese ancestry lung cancer cases, 1,006 Han Chinese ancestry non-cardia gastric cancer cases, 2,031 Han Chinese ancestry esophageal squamous-cell carcinoma cases, 4,006 Han Chinese ancestry controls 2,665 Han Chinese ancestry lung cancer cases, 3,330 Han Chinese ancestry non-cardia gastric cancer cases, 3,006 Han Chinese ancestry esophageal squamous-cell carcinoma cases, 11,436 Han Chinese ancestry controls Affymetrix [NR] 7 lung carcinoma, squamous cell carcinoma, gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0000707, http://www.ebi.ac.uk/efo/EFO_0000178 GCST001718 Genome-wide genotyping array 2015-04-29 22922875 Vithana EN 2012-08-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22922875 Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma. Glaucoma (primary angle closure) 1,281 East Asian ancestry cases, 1,987 East Asian ancestry controls, 337 South Indian ancestry cases, 2,538 South Indian ancestry controls, 236 South East Asian ancestry cases, 5,083 South East Asian ancestry controls 1,545 East Asian ancestry cases, 3,756 East Asian ancestry controls, 165 Saudi Arabian ancestry cases, 175 Saudi Arabian ancestry controls, 127 European ancestry cases, 4,703 European ancestry controls, 80 Indian ancestry cases, 309 Indian ancestry controls Illumina [493501] 5 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST001649 Genome-wide genotyping array 2013-12-11 23740937 Martin JE 2013-06-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23740937 A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci. Systemic lupus erythematosus and Systemic sclerosis up to 2,761 European ancestry systemic sclerosis cases, 769 European ancestry systemic lupus erythematosus cases, 7,381 European ancestry controls up to 1,578 European ancestry systemic sclerosis cases, 1,727 European ancestry systemic lupus erythematosus cases, 6,893 European ancestry controls Illumina [NR] 20 systemic scleroderma, systemic lupus erythematosus http://www.ebi.ac.uk/efo/EFO_0000717, http://purl.obolibrary.org/obo/MONDO_0007915 GCST002069 Genome-wide genotyping array 2012-11-15 22961080 Li H 2012-09-06 Diabetes www.ncbi.nlm.nih.gov/pubmed/22961080 A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. Type 2 diabetes 1,839 Han Chinese ancestry cases, 1,873 Han Chinese ancestry controls 15,979 East Asian ancestry cases, 19,360 East Asian ancestry controls, 794 Malay ancestry cases, 1,240 Malay ancestry controls, 159 Filipino ancestry cases, 1,624 Filipino ancestry controls Illumina [2234194] (imputed) 10 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST001666 Genome-wide genotyping array 2014-04-09 24159609 Choi H 2013-10-01 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/24159609 Genome-wide genotype-based risk model for survival in acute myeloid leukaemia patients with normal karyotype. Acute myeloid leukemia 118 Korean ancestry individuals 129 Korean ancestry individuals Affymetrix [632957] 0 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST002210 Genome-wide genotyping array 2014-02-11 19151717 Rafnar T 2009-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19151717 Sequence variants at the TERT-CLPTM1L locus associate with many cancer types. Basal cell carcinoma 1,505 European ancestry cases, 28,890 European ancestry controls 1,060 European ancestry cases, 515 European ancestry controls Illumina [302140] 1 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST000318 Genome-wide genotyping array 2013-06-05 23412934 Gourraud PA 2013-02-13 Brain www.ncbi.nlm.nih.gov/pubmed/23412934 A genome-wide association study of brain lesion distribution in multiple sclerosis. Multiple sclerosis 284 European ancestry individuals Illumina [208975] 16 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST001860 Genome-wide genotyping array 2011-02-25 21242260 Cui R 2011-01-17 Gut www.ncbi.nlm.nih.gov/pubmed/21242260 Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. Colorectal cancer 1,583 Japanese ancestry cases, 1,898 Japanese ancestry controls 4,584 Japanese ancestry cases, 225 Korean ancestry distal cases, 2,973 East Asian ancestry controls Illumina [391749] 2 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST000948 Genome-wide genotyping array 2014-03-14 23992748 Drake KA 2013-08-29 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/23992748 A genome-wide association study of bronchodilator response in Latinos implicates rare variants. Asthma (bronchodilator response) up to 1,782 Latino child cases 529 Latino child cases Affymetrix [568037] 0 response to bronchodilator http://purl.obolibrary.org/obo/GO_0097366 GCST002154 Genome-wide genotyping array 2013-05-17 23423138 Ludwig KU 2013-02-19 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/23423138 A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. Mathematical ability in children with dyslexia 200 European ancestry cases 510 European ancestry cases Illumina [NR] 1 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST001866 Genome-wide genotyping array 2014-10-17 24583629 Senapati S 2014-02-27 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/24583629 Genome-wide analysis of methotrexate pharmacogenomics in rheumatoid arthritis shows multiple novel risk variants and leads for TYMS regulation. Response to methotrexate in rheumatoid arthritis 281 Indian ancestry good responder cases, 157 Indian ancestry poor responder cases NA Illumina [432662] 2 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST002375 Genome-wide genotyping array 2015-07-10 25378659 Lemaitre RN 2014-11-06 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/25378659 Genetic loci associated with circulating levels of very long-chain saturated fatty acids. Very long-chain saturated fatty acid levels (fatty acid 20:0) 10,129 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 21 very long-chain saturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0006796 GCST002690 Genome-wide genotyping array 2015-07-10 25378659 Lemaitre RN 2014-11-06 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/25378659 Genetic loci associated with circulating levels of very long-chain saturated fatty acids. Very long-chain saturated fatty acid levels (fatty acid 22:0) 10,129 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 11 very long-chain saturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0006796 GCST002688 Genome-wide genotyping array 2015-07-10 25378659 Lemaitre RN 2014-11-06 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/25378659 Genetic loci associated with circulating levels of very long-chain saturated fatty acids. Very long-chain saturated fatty acid levels (fatty acid 24:0) 7,915 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 4 very long-chain saturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0006796 GCST002689 Genome-wide genotyping array 2014-02-04 23850713 Yang SK 2013-07-14 Gut www.ncbi.nlm.nih.gov/pubmed/23850713 Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations. Crohn's disease 532 Korean ancestry cases, 733 Korean ancestry controls 1,779 Korean ancestry cases, 1,709 Korean ancestry controls Illumina [5664371] (imputed) 8 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST002094 Genome-wide genotyping array 2014-11-09 24740154 Lange EM 2014-04-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/24740154 Genome-wide association scan for variants associated with early-onset prostate cancer. Prostate cancer (early onset) 931 European ancestry cases, 4,120 European ancestry controls 2,571 European ancestry cases, 921 European ancestry controls Illumina [2639562] (imputed) 9 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002413 Genome-wide genotyping array 2015-06-20 25072098 Bloom AJ 2014-09-01 Ann Am Thorac Soc www.ncbi.nlm.nih.gov/pubmed/25072098 Beyond cigarettes per day. A genome-wide association study of the biomarker carbon monoxide. Exhaled carbon monoxide levels 1,521 European ancestry smoker individuals, 247 African American smoker individuals NA Illumina [NR] 1 smoking behavior, carbon monoxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0006520 GCST002584 Genome-wide genotyping array 2015-07-15 25411163 Maitland ML 2014-11-19 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/25411163 Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of Pazopanib. Serum VEGFR2 concentration 736 Old Order Amish NA Affymetrix [549310] 1 serum VEGFR2 concentration measurement http://www.ebi.ac.uk/efo/EFO_0006795 GCST002698 Genome-wide genotyping array 2015-07-07 25288136 Cornelis MC 2014-10-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25288136 Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Coffee consumption (cups per day) 91,462 European ancestry individuals 30,062 European ancestry individuals, 7,964 African American individuals Affymetrix, Illumina [2373958] (imputed) 9 coffee consumption, cups of coffee per day measurement http://www.ebi.ac.uk/efo/EFO_0004330, http://www.ebi.ac.uk/efo/EFO_0006782 GCST002650 Genome-wide genotyping array 2015-07-07 25288136 Cornelis MC 2014-10-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25288136 Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption. Coffee consumption 17,479 European ancestry high consumption individuals, 31,049 European ancestry no or low consumption individuals 6,497 European ancestry high consumption individuals, 432 African American high consumption individuals, 6,972 European ancestry no or low consumption individuals, 3,413 African American no or low consumption individuals Affymetrix, Illumina [2376205] (imputed) 4 coffee consumption http://www.ebi.ac.uk/efo/EFO_0004330 GCST002651 Genome-wide genotyping array 2014-11-06 24532677 Bossini-Castillo L 2014-02-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/24532677 A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides. Rheumatoid arthritis (ACPA-negative) 1,148 European ancestry cases, 6,008 European ancestry controls 774 European ancestry cases, 1,079 European ancestry controls Illumina [452367] 6 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST002357 Genome-wide genotyping array 2015-05-18 25279986 Skibola CF 2014-10-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25279986 Genome-wide association study identifies five susceptibility loci for follicular lymphoma outside the HLA region. Follicular lymphoma 2,728 European ancestry cases, 7,758 European ancestry controls 1,795 European ancestry cases, 5,586 European ancestry controls Illumina [up to 21554489] 9 neoplasm of mature B-cells http://www.ebi.ac.uk/efo/EFO_0000096 GCST002643 Genome-wide genotyping array 2015-09-24 25378290 McQueen MB 2014-11-07 Behav Genet www.ncbi.nlm.nih.gov/pubmed/25378290 The National Longitudinal Study of Adolescent to Adult Health (Add Health) sibling pairs genome-wide data. Body mass index (change over time) 917 European ancestry individuals, 677 African American individuals, 209 Hispanic individuals, 73 Asian ancestry individuals, 8 Native American ancestry individuals, 2 individuals NA Illumina [717411] 4 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST002692 Genome-wide genotyping array 2016-02-04 25778476 Jun G 2015-03-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25778476 A novel Alzheimer disease locus located near the gene encoding tau protein. Alzheimer's disease (APOE e4 interaction) 10,352 APOE e4+ cases, 9,207 APOE e4+ controls, 7,184 APOE e4- cases, 26,968 APOE e4- controls 1,250 APOE e4+ European ancestry cases, 536 APOE e4+ European ancestry controls, 718 APOE e4- European ancestry cases, 1,699 APOE e4- European ancestry controls NR [NR] 4 Alzheimer disease, APOE carrier status http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0007659 GCST002814 Genome-wide genotyping array 2016-02-03 25778476 Jun G 2015-03-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25778476 A novel Alzheimer disease locus located near the gene encoding tau protein. Alzheimer's disease in APOE e4+ carriers 10,352 cases, 9,207 controls 1,250 European ancestry cases, 536 European ancestry controls NR [NR] 17 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002813 Genome-wide genotyping array 2016-02-03 25778476 Jun G 2015-03-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25778476 A novel Alzheimer disease locus located near the gene encoding tau protein. Alzheimer's disease in APOE e4- carriers 7,184 cases, 26,968 controls 718 European ancestry cases, 1,699 European ancestry controls NR [NR] 29 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002817 Genome-wide genotyping array 2014-12-17 24951543 Liao J 2014-06-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24951543 Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract. Age-related nuclear cataracts 2,369 Malay ancestry individuals, 2,200 Indian ancestry individuals, 2,571 Chinese ancestry individuals NA Illumina [4736131] (imputed) 15 Age-related nuclear cataract http://purl.obolibrary.org/obo/HP_0011142 GCST002498 Genome-wide genotyping array 2015-10-28 25575512 Lu W 2015-01-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25575512 Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels. Lipoprotein (a) - cholesterol levels 1,376 Old Order Amish individuals NA Affymetrix [~ 2500000] (imputed) 15 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST002746 Genome-wide genotyping array 2013-03-05 23216389 Zuo L 2012-12-06 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/23216389 Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence. Alcohol and nicotine co-dependence 818 European ancestry cases, 1,396 European ancestry controls Up to 907 European ancestry cases, up to 2,830 European ancestry controls, up to 449 African American cases, up to 480 African American controls Illumina [805814] 2 alcohol and nicotine codependence http://www.ebi.ac.uk/efo/EFO_0004776 GCST001769 Genome-wide genotyping array 2016-01-30 25781172 Avramopoulos D 2015-03-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/25781172 Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation. Schizophrenia (inflammation and infection response interaction) 460 Ashkenazi Jewish schizophrenia cases, 241 Ashkenazi Jewish controls NA Affymetrix [516638] 4 schizophrenia, HSV1 seropositivity, Toxoplasma gondii seropositivity, cytomegalovirus seropositivity http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0007050, http://www.ebi.ac.uk/efo/EFO_0007047, http://www.ebi.ac.uk/efo/EFO_0007037 GCST002812 Genome-wide genotyping array 2016-02-02 25781172 Avramopoulos D 2015-03-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/25781172 Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation. Bipolar disorder (inflammation and infection response interaction) 397 Ashkenazi Jewish bipolar disorder cases, 241 Ashkenazi Jewish controls NA Affymetrix [516638] 5 bipolar disorder, HSV1 seropositivity, cytomegalovirus seropositivity http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0007050, http://www.ebi.ac.uk/efo/EFO_0007037 GCST002815 Genome-wide genotyping array 2015-11-11 25865352 Schaarschmidt H 2015-04-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/25865352 A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis. Atopic dermatitis 870 European ancestry cases, 5,293 European ancestry controls 1,383 European ancestry cases, 1,728 European ancestry controls Affymetrix [1623390] (imputed) 6 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST002844 Genome-wide genotyping array 2016-02-10 25865494 Chan Y 2015-04-09 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25865494 Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development. Sitting height ratio 3,545 African American individuals, 12,965 European ancestry women, 8,625 European ancestry men NA Affymetrix, Illumina [up to 10250422] (imputed) 44 sitting height ratio http://www.ebi.ac.uk/efo/EFO_0007118 GCST002843 Genome-wide genotyping array 2016-02-05 25855579 Mancikova V 2015-04-22 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/25855579 Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations. Thyroid cancer 398 European ancestry cases , 502 European ancestry controls 1,422 European ancestry cases, 1,908 European ancestry controls Affymetrix [474624] 3 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST002873 Genome-wide genotyping array 2013-01-16 23108985 Guo YF 2012-10-30 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23108985 Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study. Body mass (lean) 1,627 Han Chinese individuals 2,286 European ancestry individuals Affymetrix [689368] 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST001722 Genome-wide genotyping array 2015-10-24 25884002 Moore CB 2015-01-09 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/25884002 Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols. Total bilirubin levels in HIV-1 infection 2,547 individuals NA Illumina [5954294] (imputed) 11 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST002745 Genome-wide genotyping array 2015-10-24 25884002 Moore CB 2015-01-09 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/25884002 Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols. Neutrophil count in HIV-infection 2,547 individuals NA Illumina [5954294] (imputed) 2 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST002743 Genome-wide genotyping array 2015-10-27 25884002 Moore CB 2015-01-09 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/25884002 Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols. HDL Cholesterol in HIV-infection 2,547 individuals NA Illumina [5954294] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST002744 Genome-wide genotyping array 2015-10-26 25824743 Haryono SJ 2015-01-01 Asian Pac J Cancer Prev www.ncbi.nlm.nih.gov/pubmed/25824743 A pilot genome-wide association study of breast cancer susceptibility loci in Indonesia. Breast cancer 89 Indonesian ancestry cases, 46 Indonesian ancestry controls NA Affymetrix [292887] 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST002735 Genome-wide genotyping array 2015-05-07 25208887 Ma Q 2014-09-10 Blood www.ncbi.nlm.nih.gov/pubmed/25208887 Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels. Plasma plasminogen levels up to 3,244 European ancestry individuals NA Illumina [up to 4514079] (imputed) 4 plasma plasminogen measurement http://www.ebi.ac.uk/efo/EFO_0006309 GCST002601 Genome-wide genotyping array 2015-11-14 25637336 Chan JP 2015-02-01 Age (Dordr) www.ncbi.nlm.nih.gov/pubmed/25637336 Genetics of hand grip strength in mid to late life. Hand grip strength 2,088 European ancestry individuals 541 European ancestry individuals Affymetrix [at least 549281] (imputed) 2 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST002770 Genome-wide genotyping array 2015-12-07 25890600 Guo Q 2015-04-18 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/25890600 Identification of novel genetic markers of breast cancer survival. Breast cancer (survival) 23,059 European ancestry estrogen-receptor positive cases, 6,881 European ancestry estrogen-receptor negative cases, 8,014 European ancestry cases Affymetrix, Illumina [9000000] (imputed) 3 estrogen-receptor negative breast cancer, survival time, estrogen-receptor positive breast cancer, breast carcinoma http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305 GCST002861 Genome-wide genotyping array 2015-06-22 25729143 Ahmetov I 2014-10-21 Biol Sport www.ncbi.nlm.nih.gov/pubmed/25729143 Genome-wide association study identifies three novel genetic markers associated with elite endurance performance. Maximal oxygen uptake response 15 Russian ancestry male long endurance athletes, 17 Russian ancestry female long endurance athletes, 31 Russian ancestry middle and short endurance athletes, 17 Russian ancestry middle and short endurance athletes NA Illumina [1140419] 4 maximal oxygen uptake measurement http://www.ebi.ac.uk/efo/EFO_0004887 GCST002664 Genome-wide genotyping array 2016-02-10 25888059 Cha S 2015-04-15 BMC Complement Altern Med www.ncbi.nlm.nih.gov/pubmed/25888059 The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. Sasang constitutional medicine type (So-Eum) 1,905 Korean ancestry So-Eum type individuals, 1,905 Korean ancestry non-So-Eum type individuals 840 Korean ancestry So-Eum type individuals, 840 Korean ancestry non-So-Eum type individuals Affymetrix [311944] 1 So-Eum, Sasang constitutional medicine type http://www.ebi.ac.uk/efo/EFO_0007123, http://www.ebi.ac.uk/efo/EFO_0007119 GCST002854 Genome-wide genotyping array 2016-02-10 25888059 Cha S 2015-04-15 BMC Complement Altern Med www.ncbi.nlm.nih.gov/pubmed/25888059 The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. Sasang constitutional medicine type (Tae-Eum) 1,905 Korean ancestry Tae-Eum type individuals, 1,905 Korean ancestry non-Tae-Eum type individuals 840 Korean ancestry Tae-Eum type individuals, 840 Korean ancestry non-Tae-Eum type individuals Affymetrix [311944] 0 Tae-Eum, Sasang constitutional medicine type http://www.ebi.ac.uk/efo/EFO_0007122, http://www.ebi.ac.uk/efo/EFO_0007119 GCST002853 Genome-wide genotyping array 2016-02-10 25888059 Cha S 2015-04-15 BMC Complement Altern Med www.ncbi.nlm.nih.gov/pubmed/25888059 The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. Sasang constitutional medicine type (So-Yang) 1,905 Korean ancestry So-Yang type individuals, 1,905 Korean ancestry non-So-Yang type individuals 840 Korean ancestry So-Yang type individuals, 840 Korean ancestry non-So-Yang type individuals Affymetrix [311944] 0 So-Yang, Sasang constitutional medicine type http://www.ebi.ac.uk/efo/EFO_0007121, http://www.ebi.ac.uk/efo/EFO_0007119 GCST002852 Genome-wide genotyping array 2016-02-10 25888059 Cha S 2015-04-15 BMC Complement Altern Med www.ncbi.nlm.nih.gov/pubmed/25888059 The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses. Sasang constitutional medicine type (Tae-Yang) 1,905 Korean ancestry Tae-Yang type individuals, 1,905 Korean ancestry non-Tae-Yang type individuals 840 Korean ancestry Tae-Yang type individuals, 840 Korean ancestry non-Tae-Yang type individuals Affymetrix [311944] 0 Tae-Yang, Sasang constitutional medicine type http://www.ebi.ac.uk/efo/EFO_0007120, http://www.ebi.ac.uk/efo/EFO_0007119 GCST002851 Genome-wide genotyping array 2016-01-30 25881214 Shah AA 2015-02-27 Heart Surg Forum www.ncbi.nlm.nih.gov/pubmed/25881214 Genetic variants associated with vein graft stenosis after coronary artery bypass grafting. Vein graft stenosis in coronary artery bypass grafting 361 European ancestry cases, 160 European ancestry controls NA Illumina [905781] 7 vein graft stenosis http://www.ebi.ac.uk/efo/EFO_0007051 GCST002793 Genome-wide genotyping array 2015-04-15 25111785 Jamain S 2014-08-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/25111785 Common and rare variant analysis in early-onset bipolar disorder vulnerability. Bipolar disorder (early onset) 211 European ancestry cases, 1,719 European ancestry controls 159 European ancestry cases, 998 European ancestry controls, 2,288 cases, 4,374 controls Illumina [261525] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST002564 Genome-wide genotyping array 2016-01-31 25869804 Ibrahim-Verbaas CA 2015-04-14 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25869804 GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Information processing speed Up to 30,807 European ancestry individuals, up to 1,267 Erasmus Rucphen (founder/genetic isolated) individuals, up to 535 Korculan (founder/genetic isolated) individuals, up to 417 Orcadian (founder/genetic isolated) individuals, up to 311 Vis (founder/genetic isolated) individuals Up to 8,436 European ancestry individuals, up to 1,444 African American individuals Affymetrix, Illumina [up to 2357391] (imputed) 4 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST002850 Genome-wide genotyping array 2016-01-31 25869804 Ibrahim-Verbaas CA 2015-04-14 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25869804 GWAS for executive function and processing speed suggests involvement of the CADM2 gene. Executive function Up to 10,904 European ancestry individuals, up to 1,263 Erasmus Rucphen (founder/genetic isolated) individuals, up to 495 Korculan (founder/genetic isolated) individuals, up to 418 Orcadian (founder/genetic isolated) individuals, up to 382 Vis (founder/genetic isolated) individuals Up to 20,720 European ancestry individuals, up to 3,146 African American individuals Affymetrix, Illumina [up to 2357391] (imputed) 0 executive function http://www.ebi.ac.uk/efo/EFO_0007046 GCST002849 Genome-wide genotyping array 2015-12-02 25897834 Biernacka JM 2015-04-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25897834 The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response. Response to serotonin reuptake inhibitors in major depressive disorder 298 European ancestry cases, 567 Asian ancestry cases, 1529 European and other ancestry cases NA Illumina [~ 7000000] (imputed) 20 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST002868 Genome-wide genotyping array 2015-11-18 25875332 Zayats T 2015-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/25875332 Genome-wide analysis of attention deficit hyperactivity disorder in Norway. Attention deficit hyperactivity disorder 478 European ancestry cases, 880 European ancestry controls (see Smoller, 2013) Illumina [598384] 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST002848 Genome-wide genotyping array 2015-11-20 25886283 Chang X 2015-04-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/25886283 Genome-wide association study of serum minerals levels in children of different ethnic background. Magnesium levels 2,317 European ancestry children, 1,283 African American ancestry children NA Illumina [up to 509150] 15 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST002860 Genome-wide genotyping array 2015-11-20 25886283 Chang X 2015-04-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/25886283 Genome-wide association study of serum minerals levels in children of different ethnic background. Calcium levels 5,261 European ancestry children, 3,817 African American ancestry children Illumina [up to 507950] 6 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST002857 Genome-wide genotyping array 2016-02-10 25898001 Dong C 2015-04-16 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/25898001 Genetic variants in LEKR1 and GALNT10 modulate sex-difference in carotid intima-media thickness: a genome-wide interaction study. Carotid artery intima media thickness (sex interaction) 931 Hispanic individuals 153 European ancestry individuals, 257 Black individuals Affymetrix [731037] 4 sex interaction measurement, carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0007117 GCST002856 Genome-wide genotyping array 2016-01-27 25896534 Julia A 2015-04-21 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/25896534 A genome-wide association study identifies a new locus associated with the response to anti-TNF therapy in rheumatoid arthritis. Response to anti-TNF treatment (adalimumab, etanercept or infliximab) in rheumatoid arthritis 269 European ancestry responders, 92 European ancestry non-responders 181 European ancestry responders, 64 European ancestry non-responders Illumina [511754] 0 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST002869 Genome-wide genotyping array 2016-02-05 25897833 Thompson AG 2015-04-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25897833 Genome-wide association study of behavioural and psychiatric features in human prion disease. Psychotic symptoms and prion disease Up to 170 cases, 5,200 controls NA Illumina [518938] 1 prion disease, psychotic symptoms http://www.ebi.ac.uk/efo/EFO_0004720, http://www.ebi.ac.uk/efo/EFO_0005940 GCST002871 Genome-wide genotyping array 2016-02-05 25897833 Thompson AG 2015-04-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25897833 Genome-wide association study of behavioural and psychiatric features in human prion disease. Mood disorder and prion disease Up to 170 cases, 5,200 controls NA Illumina [518938] 3 prion disease, mood disorder http://www.ebi.ac.uk/efo/EFO_0004720, http://www.ebi.ac.uk/efo/EFO_0004247 GCST002862 Genome-wide genotyping array 2016-02-05 25897833 Thompson AG 2015-04-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25897833 Genome-wide association study of behavioural and psychiatric features in human prion disease. Behavioral disturbance or psychiatric symptoms and prion disease Up to 170 cases, 5,200 controls NA Illumina [518938] 3 prion disease, Atypical behavior http://www.ebi.ac.uk/efo/EFO_0004720, http://purl.obolibrary.org/obo/HP_0000708 GCST002866 Genome-wide genotyping array 2016-02-05 25897833 Thompson AG 2015-04-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25897833 Genome-wide association study of behavioural and psychiatric features in human prion disease. Psychotic symptoms in prion disease Up to 170 cases NA Illumina [518938] 3 psychotic symptoms http://www.ebi.ac.uk/efo/EFO_0005940 GCST002867 Genome-wide genotyping array 2016-02-05 25897833 Thompson AG 2015-04-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25897833 Genome-wide association study of behavioural and psychiatric features in human prion disease. Mood disorder in prion disease Up to 170 cases NA Illumina [518938] 3 mood disorder http://www.ebi.ac.uk/efo/EFO_0004247 GCST002864 Genome-wide genotyping array 2016-02-05 25897833 Thompson AG 2015-04-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25897833 Genome-wide association study of behavioural and psychiatric features in human prion disease. Behavioral disturbance or psychiatric symptoms in prion disease Up to 170 cases NA Illumina [518938] 2 Atypical behavior http://purl.obolibrary.org/obo/HP_0000708 GCST002863 Genome-wide genotyping array 2015-11-17 25877299 Kristiansen W 2015-04-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25877299 Two new loci and gene sets related to sex determination and cancer progression are associated with susceptibility to testicular germ cell tumor. Testicular germ cell tumor 1,326 European ancestry cases, 6,687 European ancestry controls 710 European ancestry case-parent triads, 289 European ancestry cases, 290 European ancestry controls Illumina [610240] 8 Testicular Germ Cell Tumor http://www.ebi.ac.uk/efo/EFO_1000566 GCST002855 Genome-wide genotyping array 2016-02-05 25867717 Song N 2015-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/25867717 Prediction of breast cancer survival using clinical and genetic markers by tumor subtypes. Disease-free survival in breast cancer 1,732 Korean ancestry cases 1,494 Korean ancestry cases Affymetrix [2210580] (imputed) 2 disease free survival, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000409, http://www.ebi.ac.uk/efo/EFO_0000305 GCST002847 Genome-wide genotyping array 2015-11-14 25848760 Sun Y 2015-04-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/25848760 A common variant of ubiquinol-cytochrome c reductase complex is associated with DDH. Developmental dysplasia of the hip 386 Han Chinese ancestry cases, 558 Han Chinese ancestry controls 755 Han Chinese ancestry cases, 944 Han Chinese ancestry controls Illumina [704516] 1 developmental dysplasia of the hip http://www.ebi.ac.uk/efo/EFO_1000648 GCST002841 Genome-wide genotyping array 2016-02-04 25898129 Shim H 2015-04-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/25898129 A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians. LDL cholesterol subfractions 1,868 European ancestry individuals 6,745 European ancestry individuals Illumina [7836525] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST002870 Genome-wide genotyping array 2016-02-04 25898129 Shim H 2015-04-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/25898129 A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians. Response to statin therapy (LDL cholesterol subfractions) 1,868 European ancestry individuals 6,745 European ancestry individuals Illumina [7836525] (imputed) 0 response to statin, low density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0004611 GCST002865 Genome-wide genotyping array 2012-11-21 22916037 Inouye M 2012-08-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22916037 Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. Metabolite levels 6,608 European ancestry individuals NA Illumina [~ 2000000] (imputed) 34 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST001639 Genome-wide genotyping array 2016-02-10 25896417 Nakada TA 2015-04-17 J Innate Immun www.ncbi.nlm.nih.gov/pubmed/25896417 VPS13D Gene Variant Is Associated with Altered IL-6 Production and Mortality in Septic Shock. Cytokine-stimulated IL-6 production 60 European ancestry lymphoblastoid cell lines NA Illumina [2300000] 2 interleukin-6 measurement, response to cytokine http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0034097 GCST002859 Genome-wide genotyping array 2016-02-10 25896417 Nakada TA 2015-04-17 J Innate Immun www.ncbi.nlm.nih.gov/pubmed/25896417 VPS13D Gene Variant Is Associated with Altered IL-6 Production and Mortality in Septic Shock. Cytokine and corticosteroid-stimulated IL-6 production 60 European ancestry lymphoblastoid cell lines NA Illumina [2300000] 2 interleukin-6 measurement, response to corticosteroid, response to cytokine http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0031960, http://purl.obolibrary.org/obo/GO_0034097 GCST002858 Genome-wide genotyping array 2016-02-04 25918517 Yashin AI 2015-04-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/25918517 Genetics of aging, health, and survival: dynamic regulation of human longevity related traits. Lifespan 679 female individuals 432 male individuals Affymetrix [429783] 7 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST002846 Genome-wide genotyping array 2009-01-07 19060909 Bouatia-Naji N 2008-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/19060909 A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. Fasting plasma glucose 2,151 European ancestry individuals 16,094 European ancestry individuals Illumina [308846] 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST000291 Genome-wide genotyping array 2015-06-20 25234806 Dijkstra AE 2014-09-18 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/25234806 Dissecting the genetics of chronic mucus hypersecretion in smokers with and without COPD. Chronic mucus hypersecretion in chronic obstructive pulmonary disease 338 European ancestry cases, 511 European ancestry controls 1,198 European ancestry cases, 1,908 European ancestry controls Illumina [522636] 0 chronic mucus hypersecretion http://www.ebi.ac.uk/efo/EFO_0005673 GCST002612 Genome-wide genotyping array 2015-06-22 25234806 Dijkstra AE 2014-09-18 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/25234806 Dissecting the genetics of chronic mucus hypersecretion in smokers with and without COPD. Chronic mucus hypersecretion 342 European ancestry cases, 1,006 European ancestry controls 130 European ancestry cases, 2,313 European ancestry controls Illumina [522636] 4 chronic mucus hypersecretion http://www.ebi.ac.uk/efo/EFO_0005673 GCST002613 Genome-wide genotyping array 2014-12-17 24974847 Fachal L 2014-06-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24974847 A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1. Response to radiotherapy in prostate cancer (toxicity) Up to 652 European ancestry cases 849 European ancestry cases Affymetrix [552597] 1 response to radiation http://purl.obolibrary.org/obo/GO_0009314 GCST002511 Genome-wide genotyping array 2014-10-09 24478790 Lee JH 2014-01-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/24478790 Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study. Telomere length 4,829 European ancestry individuals from 586 families with exceptional longevity NA Illumina [9250000] (imputed) 8 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST002336 Genome-wide genotyping array 2015-04-22 21278746 Lindstrom S 2011-01-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21278746 Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. Percent mammographic density 4,877 European ancestry females 1,145 European ancestry females, 1,690 females Affymetrix, Illumina [> 2000000] (imputed) 1 mammographic density measurement http://www.ebi.ac.uk/efo/EFO_0005941 GCST000958 Genome-wide genotyping array 2015-02-04 24999842 Garner C 2014-07-07 PLoS One www.ncbi.nlm.nih.gov/pubmed/24999842 Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus. Celiac disease 1,550 European ancestry cases, 3,084 European ancestry controls NA Illumina [517345] 8 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST002520 Genome-wide genotyping array 2015-04-23 25105248 Wang H 2014-08-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25105248 Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A. Colorectal cancer 2,627 Japanese ancestry cases, 3,797 Japanese ancestry controls, 1,893 African American cases, 4,703 African American controls 16,823 European ancestry cases, 18,211 European ancestry controls Illumina [4276079] (imputed) 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002561 Genome-wide genotyping array 2014-10-10 24514567 Boraska V 2014-02-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24514567 A genome-wide association study of anorexia nervosa. Anorexia nervosa 2,907 European ancestry cases, 14,860 European ancestry controls 2,677 European ancestry cases, 8,629 European ancestry controls, 458 Japanese ancestry cases, 421 Japanese ancestry controls Illumina [1185559] (imputed) 2 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST002354 Genome-wide genotyping array 2014-10-22 24528284 Ji Y 2014-08-01 Br J Clin Pharmacol www.ncbi.nlm.nih.gov/pubmed/24528284 Citalopram and escitalopram plasma drug and metabolite concentrations: genome-wide associations. Response to serotonin reuptake inhibitors in major depressive disorder (plasma drug and metabolite levels) 300 European ancestry Escitalpram treated individuals, 130 European ancestry Citalopram treated individuals NA Illumina [7537437] (imputed) 15 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST002549 Genome-wide genotyping array 2013-05-14 23408455 Wakai K 2013-02-14 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/23408455 Genome-wide association study of genetic factors related to confectionery intake: potential roles of the ADIPOQ gene. Confectionary intake 939 Japanese ancestry individuals 4,491 Japanese ancestry individuals Illumina [491738] 0 energy intake http://www.ebi.ac.uk/efo/EFO_0003939 GCST001861 Genome-wide genotyping array 2012-11-02 22941190 Holliday EG 2012-09-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22941190 Common variants at 6p21.1 are associated with large artery atherosclerotic stroke. Stroke (ischemic) 421 European ancestry large artery atherosclerosis cases, 741 European ancestry ischemic stroke cases, 1,244 European ancestry controls 1,715 European ancestry large artery atherosclerosis cases, 9,552 European ancestry ischemic stroke cases, 52,695 European ancestry controls Illumina [551514] 1 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST001659 Genome-wide genotyping array 2011-10-07 21909108 Bis JC 2011-09-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21909108 Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque. Carotid intima media thickness Up to 31,211 European ancestry individuals 10,553 European ancestry individuals, 687 Orcadian individuals Affymetrix, Illumina [~ 2500000] (imputed) 11 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST001231 Genome-wide genotyping array 2014-11-02 24662972 Figueroa JD 2014-03-24 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/24662972 Genome-wide interaction study of smoking and bladder cancer risk. Bladder cancer (smoking interaction) 560 European ancestry never smoker cases, 2,442 European ancestry ever smoker cases, 1,406 European ancestry never smoker controls, 3,005 European ancestry ever smoker controls 494 European ancestry never smoker cases, 1,927 European ancestry ever smoker cases, 2,257 European ancestry never smoker controls, 3,490 European ancestry ever smoker controls Illumina [491011] 5 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST002397 Genome-wide genotyping array 2014-10-02 24403052 Stacey SN 2014-01-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24403052 Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma. Basal cell carcinoma 4,208 European ancestry cases, 109,408 European ancestry controls up to 1,480 European ancestry cases, up to 4,610 European ancestry controls Illumina [38500000] (imputed) 11 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST002331 Genome-wide genotyping array 2012-11-28 22945461 Rahmioglu N 2012-09-04 Eur J Drug Metab Pharmacokinet www.ncbi.nlm.nih.gov/pubmed/22945461 Genome-wide association study reveals a complex genetic architecture underpinning-induced CYP3A4 enzyme activity. CYP3A4 enzyme activity 310 European ancestry female twin individuals NA Illumina [NR] 0 CYP3A4 activity http://www.ebi.ac.uk/efo/EFO_0004910 GCST001661 Genome-wide genotyping array 2013-09-06 19954339 Yin CS 2009-12-01 J Altern Complement Med www.ncbi.nlm.nih.gov/pubmed/19954339 Genome-wide association study of the four-constitution medicine. Sasang constitutional medicine type 60 Korean ancestry individuals NA Illumina [353202] 0 Sasang constitutional medicine http://www.ebi.ac.uk/efo/EFO_0004892 GCST000536 Genome-wide genotyping array 2013-03-19 23222517 van der Harst P 2012-12-05 Nature www.ncbi.nlm.nih.gov/pubmed/23222517 Seventy-five genetic loci influencing the human red blood cell. Red blood cell traits 62,553 European ancestry individuals, 9,308 South Asian ancestry individuals 63,506 European ancestry individuals Affymetrix, Illumina, Perlegen [2711806] (imputed) 45 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST001765 Genome-wide genotyping array 2014-11-14 24782177 Jiang L 2014-05-01 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/24782177 Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans. Rheumatoid arthritis 433 Han Chinese ancestry ACPA positive cases, 519 Han Chinese ancestry ACPA negative cases, 943 Han Chinese ancestry controls 1,032 Han Chinese ancestry ACPA positive cases, 1,100 Han Chinese ancestry ACPA negative cases, 2,553 Han Chinese ancestry controls Affymetrix [3441843] (imputed) 11 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST002433 Genome-wide genotyping array 2014-11-14 24782177 Jiang L 2014-05-01 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/24782177 Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans. Rheumatoid arthritis 952 Han Chinese ancestry cases, 943 Han Chinese ancestry controls 5,539 European ancestry cases, 20,169 European ancestry controls Affymetrix [1497047] (imputed) 4 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST002434 Genome-wide genotyping array 2014-03-22 24014518 Kasperaviciute D 2013-09-06 Brain www.ncbi.nlm.nih.gov/pubmed/24014518 Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Mesial temporal lobe epilepsy with hippocampal sclerosis up to 1,018 European ancestry cases, 7,552 European ancestry controls 959 European ancestry cases, 3,591 European ancestry controls Illumina [531164] 2 mesial temporal lobe epilepsy with hippocampal sclerosis http://purl.obolibrary.org/obo/MONDO_0020476 GCST002170 Genome-wide genotyping array 2014-03-18 23996088 Migliorini G 2013-08-30 Blood www.ncbi.nlm.nih.gov/pubmed/23996088 Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype. Acute lymphoblastic leukemia (B-cell precursor) 1,658 European ancestry child cases, 4,723 European ancestry controls 1,449 European ancestry child cases, 1,488 European ancestry controls Illumina [382776] (imputed) 6 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST002158 Genome-wide genotyping array 2015-07-08 25140149 Hohman TJ 2014-08-04 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/25140149 Genetic variation modifies risk for neurodegeneration based on biomarker status. Left inferior lateral ventricle volume (Cerebrospinal fluid biomarker status interaction) 382 European ancestry mild cognitive impairment cases, 114 European ancestry Alzheimer's disease cases, 194 European ancestry controls NA Illumina [296267] 4 cerebrospinal fluid biomarker measurement, left inferior lateral ventricle volume measurement http://www.ebi.ac.uk/efo/EFO_0006794, http://www.ebi.ac.uk/efo/EFO_0006793 GCST002554 Genome-wide genotyping array 2011-11-18 21993531 Kuparinen T 2011-10-13 Genes Immun www.ncbi.nlm.nih.gov/pubmed/21993531 Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response. Cytomegalovirus antibody response 1,485 European ancestry sero-postitive individuals, 648 European ancestry sero-negative individuals NA Illumina [546677] 9 response to virus http://purl.obolibrary.org/obo/GO_0009615 GCST001272 Genome-wide genotyping array 2015-04-23 25231870 Perry JR 2014-07-23 Nature www.ncbi.nlm.nih.gov/pubmed/25231870 Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Menarche (age at onset) Up to 182,413 European ancestry females NA Affymetrix, Illumina [2441815] (imputed) 122 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST002541 Genome-wide genotyping array 2015-11-14 25784220 Sharma S 2015-03-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25784220 A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females. Adolescent idiopathic scoliosis 371 European ancestry female cases, 76 European ancestry male cases, 533 European ancestry female controls, 204 European ancestry male controls 715 European, Black, Hispanic and other ancestry trios, 216 European ancestry cases, 336 European ancestry controls, 1,050 Japanese ancestry female cases, 1,474 Japanese ancestry female controls Illumina [727670] 1 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST002819 Genome-wide genotyping array 2014-03-04 23990791 Thun GA 2013-08-22 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23990791 Causal and synthetic associations of variants in the SERPINA gene cluster with alpha1-antitrypsin serum levels. Serum alpha1-antitrypsin levels 1,392 European ancestry individuals 12,518 European ancestry individuals Illumina [2168668] (imputed) 0 serum alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0005415 GCST002146 Genome-wide genotyping array 2012-10-17 22915352 Power RA 2012-08-22 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/22915352 Dissecting the genetic heterogeneity of depression through age at onset. Depression (age of onset) Up to 2,746 European ancestry cases, 1,584 European ancestry controls 1383 European ancestry cases, 1403 European ancestry controls Illumina [471581] 0 unipolar depression, age at onset http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004847 GCST001643 Genome-wide genotyping array 2012-12-06 23028341 Yang X 2012-09-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23028341 Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. Complement C3 and C4 levels 1,999 Han Chinese ancestry male individuals 1,496 Han Chinese ancestry male individuals Illumina [1940245] (imputed) 10 complement C4 measurement, complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004984, http://www.ebi.ac.uk/efo/EFO_0004983 GCST001679 Genome-wide genotyping array 2015-04-15 24882193 Winham SJ 2014-04-19 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/24882193 Bipolar disorder with comorbid binge eating history: a genome-wide association study implicates APOB. Binge eating behaviour in bipolar disorder 206 European ancestry cases with binge eating behavior, 723 European ancestry cases without binge eating behavior 70 European ancestry cases with binge eating behavior, 758 European ancestry cases without binge eating behavior Affymetrix [8466825] (imputed) 1 binge eating http://www.ebi.ac.uk/efo/EFO_0005924 GCST002420 Genome-wide genotyping array 2015-04-15 24882193 Winham SJ 2014-04-19 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/24882193 Bipolar disorder with comorbid binge eating history: a genome-wide association study implicates APOB. Binge eating behaviour and bipolar disorder 206 European ancestry cases with binge eating behavior, 723 European ancestry cases without binge eating behavior, 1,034 European ancestry controls 70 European ancestry cases with binge eating behavior, 758 European ancestry cases without binge eating behavior, 832 European ancestry controls Affymetrix [8466825] (imputed) 2 binge eating, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0005924, http://purl.obolibrary.org/obo/MONDO_0004985 GCST002419 Genome-wide genotyping array 2014-11-02 24658283 Zhang R 2014-03-22 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/24658283 A genome-wide gene-environment interaction analysis for tobacco smoke and lung cancer susceptibility. Lung cancer (smoking interaction) 1,506 Han Chinese ancestry smoker cases, 825 Han Chinese ancestry non-smoker cases, 1,309 Han Chinese ancestry smoker controls, 1,768 Han Chinese ancestry non-smoker controls 912 Han Chinese ancestry smoker cases, 622 Han Chinese ancestry non-smoker cases, 572 Han Chinese ancestry smoker controls, 917 Han Chinese ancestry non-smoker controls Affymetrix [591370] 2 smoking status measurement, lung carcinoma http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0001071 GCST002392 Genome-wide genotyping array 2013-02-08 23207799 Deng FY 2012-11-30 Bone www.ncbi.nlm.nih.gov/pubmed/23207799 Genome-wide association study identified UQCC locus for spine bone size in humans. Spine bone size 2,286 European ancestry individuals 2,503 European ancestry individuals, 1,627 Han Chinese ancestry individuals Affymetrix [746709] 1 spine bone size http://www.ebi.ac.uk/efo/EFO_0004508 GCST001756 Genome-wide genotyping array 2015-06-25 23247143 Yu B 2012-12-16 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23247143 Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. Cardiac Troponin-T levels 9,491 European ancestry individuals, up to 2,053 African American individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 18 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST001776 Genome-wide genotyping array 2014-11-08 24709693 Cobb J 2014-04-08 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/24709693 Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases. Response to methotrexate in juvenile idiopathic arthritis 694 European ancestry child cases NA Illumina [586062] 18 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST002408 Genome-wide genotyping array 2013-02-28 23207651 Davies G 2012-12-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/23207651 A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing. Cognitive decline 3,280 European ancestry individuals 1,367 European ancestry individuals Illumina [549692] 1 Mental deterioration http://purl.obolibrary.org/obo/HP_0001268 GCST001761 Genome-wide genotyping array 2012-10-13 22923054 Chen F 2012-08-25 Hum Genet www.ncbi.nlm.nih.gov/pubmed/22923054 A genome-wide association study of breast cancer in women of African ancestry. Breast cancer 3,016 African American cases, 2,745 African American controls 3,533 African ancestry cases, 11,046 African ancestry controls Illumina [2067098] (imputed) 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST001648 Genome-wide genotyping array 2014-07-02 21156761 Padyukov L 2010-12-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/21156761 A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. Rheumatoid arthritis 1,147 European ancestry ACPA positive RA cases, 774 European ancestry ACPA negative RA cases, 1,079 European ancestry controls 887 European ancestry ACPA positive RA cases, 1,218 European ancestry controls Illumina [1723056] (imputed) 16 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000917 Genome-wide genotyping array 2012-10-23 22923026 Cheng I 2012-08-24 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/22923026 Evaluating genetic risk for prostate cancer among Japanese and Latinos. Prostate cancer 1,033 Japanese ancestry cases, 1,042 Japanese ancestry controls, 1,043 Latino cases, 1,057 Latino controls 1,583 Japanese ancestry cases, 3,386 Japanese ancestry controls, 1,854 European ancestry cases, 3,748 European ancestry controls Illumina [528023] 8 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001646 Genome-wide genotyping array 2014-11-21 24850809 Verweij N 2014-05-21 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24850809 Genetic determinants of P wave duration and PR segment. P wave duration 16,468 European ancestry individuals NA Illumina [2300000] (imputed) 3 P wave duration http://www.ebi.ac.uk/efo/EFO_0005094 GCST002457 Genome-wide genotyping array 2014-11-21 24850809 Verweij N 2014-05-21 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/24850809 Genetic determinants of P wave duration and PR segment. PR segment duration 16,468 European ancestry individuals NA Illumina [2300000] (imputed) 8 PR segment http://www.ebi.ac.uk/efo/EFO_0005095 GCST002456 Genome-wide genotyping array 2014-03-14 23984888 Himes BE 2013-08-28 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/23984888 ITGB5 and AGFG1 variants are associated with severity of airway responsiveness. Airway hyperresponsiveness 994 European ancestry asthma cases 650 European ancestry asthma cases, 3,354 European ancestry chronic obstructive pulmonary disease cases Affymetrix [2154322] (imputed) 1 airway hyperresponsiveness http://www.ebi.ac.uk/efo/EFO_0005414 GCST002152 Genome-wide genotyping array 2013-03-21 23263445 Lawrance-Owen AJ 2012-12-22 Hum Genet www.ncbi.nlm.nih.gov/pubmed/23263445 Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio. Digit length ratio 979 European ancestry individuals (see Medland, 2010) Illumina [642758] 1 digit length ratio http://www.ebi.ac.uk/efo/EFO_0004841 GCST001788 Genome-wide genotyping array 2014-03-13 23953852 Pan Y 2013-08-13 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/23953852 Genome-wide association studies of maximum number of drinks. Alcohol consumption 2,687 European ancestry individuals 3,137 European ancestry individuals Illumina [up to 818773] 0 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST002121 Genome-wide genotyping array 2015-04-01 25130324 Cai DC 2014-08-29 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/25130324 A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus. Heschl's gyrus morphology 1,778 European ancestry individuals, 1,276 individuals NA Affymetrix, Illumina [4103035] (imputed) 33 Heschl's gyrus morphology measurement http://www.ebi.ac.uk/efo/EFO_0005852 GCST002579 Genome-wide genotyping array 2011-01-03 21037568 Enciso-Mora V 2010-10-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21037568 A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3). Hodgkin's lymphoma 589 European ancestry cases, 5,199 European ancestry controls 2,057 European ancestry cases, 3,416 European ancestry controls Illumina [504374] 5 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST000851 Genome-wide genotyping array 2014-05-13 24149102 Frampton M 2013-10-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24149102 Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. Hodgkin's lymphoma 1,465 European ancestry cases, 6,417 European ancestry controls 1,071 European ancestry cases, 953 cases, 1,853 controls Illumina [296129] 6 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST002237 Genome-wide genotyping array 2015-08-09 25477429 Lieb W 2014-12-04 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/25477429 Genome-wide meta-analyses of plasma renin activity and concentration reveal association with the kininogen 1 and prekallikrein genes. Plasma renin activity levels 5,275 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 3 plasma renin activity measurement http://www.ebi.ac.uk/efo/EFO_0006828 GCST002714 Genome-wide genotyping array 2015-02-04 24993907 Smolonska J 2014-07-03 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/24993907 Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis. Asthma or chronic obstructive pulmonary disease 920 European ancestry Asthma cases, 1,030 European ancestry Chronic obstructive pulmonary disease cases, 4,585 European ancestry controls 461 European ancestry Asthma cases, 118 European ancestry Chronic obstructive pulmonary disease cases, 656 European ancestry controls, 720 European, African American and Hispanic Asthma cases, 1,019 European, African American and Hispanic Chronic obstructive pulmonary disease cases, 19,173 European, African American and Hispanic controls, 1,106 Asthma cases, 1,806 Chronic obstructive pulmonary disease cases, 18,580 controls Illumina [1811026] 3 asthma, chronic obstructive pulmonary disease http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0000341 GCST002519 Genome-wide genotyping array 2015-07-09 25221879 Wu K 2014-09-15 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/25221879 Genome-wide interrogation of longitudinal FEV1 in children with asthma. Pulmonary function in asthmatics 510 European ancestry NA Illumina [473680] 6 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST002608 Genome-wide genotyping array 2015-12-18 25742292 Aschebrook-Kilfoy B 2015-03-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/25742292 Genome-wide association study of parity in Bangladeshi women. Number of children (6+ vs. 0 or 1) 1,686 Bangladeshi women NA Illumina [1211988] (imputed) 11 female fertility, fertility measurement http://www.ebi.ac.uk/efo/EFO_0006918, http://www.ebi.ac.uk/efo/EFO_0006923 GCST002800 Genome-wide genotyping array 2015-12-18 25742292 Aschebrook-Kilfoy B 2015-03-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/25742292 Genome-wide association study of parity in Bangladeshi women. Number of children 1,686 Bangladeshi women NA Illumina [1211988] (imputed) 8 female fertility, fertility measurement http://www.ebi.ac.uk/efo/EFO_0006918, http://www.ebi.ac.uk/efo/EFO_0006923 GCST002801 Genome-wide genotyping array 2015-12-18 25742292 Aschebrook-Kilfoy B 2015-03-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/25742292 Genome-wide association study of parity in Bangladeshi women. Number of pregnancies 1,686 Bangladeshi women NA Illumina [1211988] (imputed) 12 female fertility, fertility measurement http://www.ebi.ac.uk/efo/EFO_0006918, http://www.ebi.ac.uk/efo/EFO_0006923 GCST002799 Genome-wide genotyping array 2015-07-17 25431337 Bouzigon E 2014-11-27 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/25431337 A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults. Fractional exhaled nitric oxide levels 610 European ancestry adult individuals, 601 Hutterite (founder/genetic isolate) adult individuals 450 Talana (founder/genetic isolate) adult individuals, 8,858 European ancestry children Affymetrix, Illumina [247463] (imputed) 2 nitric oxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0005536 GCST002704 Genome-wide genotyping array 2015-12-18 25760438 Anderson D 2015-03-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/25760438 First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes. Body mass index 361 Martu Australian Aboriginal ancestry individuals NA Illumina [1075436] (imputed) 11 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST002805 Genome-wide genotyping array 2015-12-18 25760438 Anderson D 2015-03-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/25760438 First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes. Type 2 diabetes 89 Martu Australian Aboriginal ancestry cases, 302 Martu Australian Aboriginal ancestry controls NA Illumina [1075436] (imputed) 17 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002806 Genome-wide genotyping array 2015-01-21 24978480 Real LM 2014-06-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/24978480 A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. Colorectal cancer (SNP x SNP interaction) 480 European ancestry cases, 801 European ancestry controls 1,305 European ancestry cases, 2,049 European ancestry controls Affymetrix [178930] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002513 Genome-wide genotyping array 2015-01-21 24978480 Real LM 2014-06-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/24978480 A colorectal cancer susceptibility new variant at 4q26 in the Spanish population identified by genome-wide association analysis. Colorectal cancer 480 European ancestry cases, 801 European ancestry controls 1,305 European ancestry cases, 2,049 European ancestry controls Affymetrix [178930] 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002512 Genome-wide genotyping array 2015-07-27 25468567 Perez-Andreu V 2014-12-02 Blood www.ncbi.nlm.nih.gov/pubmed/25468567 A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults. Acute lymphoblastic leukemia (adolescents and young adults) 99 European ancestry cases, 1,381 European ancestry controls, 15 African American cases, 1,363 African American controls, 76 Hispanic cases, 1,008 Hispanic controls, 118 other ancestry cases, 2,909 other ancestry controls 72 European ancestry cases, 3,667 European ancestry controls, 9 African American cases, 1,076 African American controls, 34 Hispanic cases, 501 Hispanic controls, 47 other ancestry cases, 511 other ancestry controls Affymetrix [635297] 1 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST002713 Genome-wide genotyping array 2015-10-24 25566987 Hosgood HD 3rd 2015-01-08 Hum Genet www.ncbi.nlm.nih.gov/pubmed/25566987 Interactions between household air pollution and GWAS-identified lung cancer susceptibility markers in the Female Lung Cancer Consortium in Asia (FLCCA). Lung cancer (household air pollution interaction) 1,731 Asian ancestry never smoker cases, 1,349 Asian ancestry never smoker controls NA Illumina [NR] 0 lung carcinoma, household air pollution measurement http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0006924 GCST002739 Genome-wide genotyping array 2015-11-28 25758996 Pirastu N 2015-03-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25758996 Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking. Red wine liking 398 Carlantino (founder/genetic isolated) individuals, 751 Friuli Venezia Giulia (founder/genetic isolated) individuals, 1,122 Val Borbera (founder/genetic isolated) individuals 1,246 Erasmus Rucphen (founder/genetic isolated) individuals, 353 Silk Road individuals Illumina [6967159] (imputed) 2 red wine liking measurement http://www.ebi.ac.uk/efo/EFO_0006947 GCST002803 Genome-wide genotyping array 2015-11-28 25758996 Pirastu N 2015-03-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25758996 Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking. White wine liking 381 Carlantino (founder/genetic isolated) individuals, 744 Friuli Venezia Giulia (founder/genetic isolated) individuals, 1,115 Val Borbera (founder/genetic isolated) individuals 1,261 Erasmus Rucphen (founder/genetic isolated) individuals, 335 Silk Road individuals Illumina [9969492] (imputed) 2 white wine liking measurement http://www.ebi.ac.uk/efo/EFO_0006948 GCST002802 Genome-wide genotyping array 2013-03-05 23263487 Jia WH 2012-12-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23263487 Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer. Colorectal cancer 2,098 East Asian ancestry cases, 5,749 East Asian ancestry controls 5,358 East Asian ancestry cases, 5,922 East Asian ancestry controls, 26,060 European ancestry individuals Affymetrix, Illumina [1636380] (imputed) 7 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST001792 Genome-wide genotyping array 2015-06-26 25344690 Feenstra B 2014-10-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25344690 Common variants associated with general and MMR vaccine-related febrile seizures. Febrile seizures 929 European ancestry MMR vaccine-related febrile seizures cases, 1,070 European ancestry MMR vaccine-unrelated febrile seizures cases, 4,118 European ancestry controls Up to 408 European ancestry MMR vaccine-related febrile seizures cases, Up to 1,034 European ancestry MMR vaccine-unrelated febrile seizures cases, Up to 1,645 European ancestry controls Illumina [up to 8129553] (imputed) 7 Febrile seizure (within the age range of 3 months to 6 years) http://purl.obolibrary.org/obo/HP_0002373 GCST002672 Genome-wide genotyping array 2015-06-26 25344690 Feenstra B 2014-10-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25344690 Common variants associated with general and MMR vaccine-related febrile seizures. Febrile seizures (MMR vaccine-unrelated) 1,070 European ancestry cases, 4,118 European ancestry controls Up to 1,034 European ancestry cases, Up to 1,645 European ancestry controls Illumina [8129384] (imputed) 4 Febrile seizure (within the age range of 3 months to 6 years) http://purl.obolibrary.org/obo/HP_0002373 GCST002673 Genome-wide genotyping array 2015-06-26 25344690 Feenstra B 2014-10-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25344690 Common variants associated with general and MMR vaccine-related febrile seizures. Febrile seizures (MMR vaccine-related) 929 European ancestry cases, 4,118 European ancestry controls Up to 408 European ancestry cases, Up to 1,645 European ancestry controls Illumina [8129524] (imputed) 10 MMR-related febrile seizures http://www.ebi.ac.uk/efo/EFO_0006519 GCST002674 Genome-wide genotyping array 2016-01-27 25786224 Johnson EO 2015-03-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25786224 Novel genetic locus implicated for HIV-1 acquisition with putative regulatory links to HIV replication and infectivity: a genome-wide association study. HIV-1 susceptibility 628 African American high risk-cases, 1,376 African American high-risk controls, 327 European ancestry high-risk cases, 805 European ancestry high-risk controls 1,395 African American high-risk cases, 457 African American high-risk controls, 513 European ancestry high-risk cases, 168 European ancestry high-risk controls Illumina [~ 8000000] (imputed) 7 HIV-1 infection, Susceptibility to viral and mycobacterial infections http://www.ebi.ac.uk/efo/EFO_0000180, http://www.orpha.net/ORDO/Orphanet_391311 GCST002818 Genome-wide genotyping array 2015-11-21 25775280 Sun Y 2015-03-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25775280 Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate. Nonsyndromic cleft lip with or without cleft palate 858 Chinese ancestry cases, 1,248 Chinese ancestry controls 1,663 Chinese ancestry cases, 1,874 Chinese ancestry controls Affymetrix [842556] 6 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST002811 Genome-wide genotyping array 2016-01-21 25758998 Rubicz R 2015-03-11 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25758998 Genome-wide genetic investigation of serological measures of common infections. Antibody level in response to infection 1,932 Mexican American individuals NA Illumina [944565] 7 seropositivity measurement http://www.ebi.ac.uk/efo/EFO_0007034 GCST002804 Genome-wide genotyping array 2015-11-12 25772935 Germain M 2015-03-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25772935 Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism. Venous thromboembolism 7,507 European ancestry cases, 52,632 European ancestry controls 3,009 European ancestry cases, 2,586 European ancestry controls Affymetrix, Illumina [6751884] (imputed) 10 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST002808 Genome-wide genotyping array 2015-10-24 25599974 Zhang H 2015-01-19 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25599974 A genome-wide association study of early spontaneous preterm delivery. Spontaneous preterm birth (preterm birth) 916 pre-term birth neonates, 935 term birth neonates 243 pre-term birth neonates, 149 term birth neonates Affymetrix [797196] 5 birth measurement, spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006921, http://www.ebi.ac.uk/efo/EFO_0006917 GCST002751 Genome-wide genotyping array 2015-10-24 25599974 Zhang H 2015-01-19 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25599974 A genome-wide association study of early spontaneous preterm delivery. Spontaneous preterm birth (preterm delivery) 935 pre-term delivery mothers, 946 term delivery mothers 66 European ancestry pre-term delivery mothers, 110 African American pre-term delivery mothers, 110 Hispanic pre-term delivery mothers, 7 pre-term delivery mothers, 37 European ancestry term delivery mothers, 84 African American term delivery mothers, 74 Hispanic term delivery mothers, 5 term delivery mothers Affymetrix [779326] 2 delivery measurement, spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006922, http://www.ebi.ac.uk/efo/EFO_0006917 GCST002752 Genome-wide genotyping array 2016-01-15 25798622 Knowles JW 2015-03-23 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/25798622 Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene. Insulin resistance/response 2,764 European ancestry individuals 1,601 Hispanic ancestry individuals, 1,259 European ancestry individuals Affymetrix, Illumina [12106458] (imputed) 1 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST002825 Genome-wide genotyping array 2015-07-27 25670933 Hanchard NA 2014-11-07 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/25670933 A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease. Alloimmunization response to red blood cell transfusion in sickle cell anemia 48 African American responder cases, 46 African American non-responder cases NA Illumina [1008655] 1 alloimmunization, response to red blood cell transfusion http://www.ebi.ac.uk/efo/EFO_0006804, http://www.ebi.ac.uk/efo/EFO_0006802 GCST002691 Genome-wide genotyping array 2016-01-25 25811787 Huffman JE 2015-03-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/25811787 Modulation of genetic associations with serum urate levels by body-mass-index in humans. Urate levels in lean individuals up to 5,529 European ancestry male individuals, up to 9,753 European ancestry female individuals NA Affymetrix, Illumina [at least 188473] (imputed) 36 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST002830 Genome-wide genotyping array 2016-01-22 25811787 Huffman JE 2015-03-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/25811787 Modulation of genetic associations with serum urate levels by body-mass-index in humans. Urate levels (BMI interaction) up to 15,007 European ancestry male individuals, up to 16,943 European ancestry female individuals NA Affymetrix, Illumina [at least 188473] (imputed) 16 urate measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004531, http://www.ebi.ac.uk/efo/EFO_0004340 GCST002826 Genome-wide genotyping array 2016-01-25 25811787 Huffman JE 2015-03-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/25811787 Modulation of genetic associations with serum urate levels by body-mass-index in humans. Urate levels in overweight individuals up to 10,058 European ancestry male individuals, up to 7,189 European ancestry female individuals NA Affymetrix, Illumina [at least 188473] (imputed) 43 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST002829 Genome-wide genotyping array 2016-01-22 25811787 Huffman JE 2015-03-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/25811787 Modulation of genetic associations with serum urate levels by body-mass-index in humans. Urate levels in obese individuals 4,613 European ancestry male individuals, 4,690 European ancestry female individuals, 142 European ancestry individuals NA Affymetrix, Illumina [at least 188473] (imputed) 35 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST002828 Genome-wide genotyping array 2016-01-22 25811787 Huffman JE 2015-03-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/25811787 Modulation of genetic associations with serum urate levels by body-mass-index in humans. Urate levels (BMI interaction) 28,610 European ancestry individuals 13,959 European ancestry individuals Affymetrix, Illumina [at least 188473] (imputed) 6 urate measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004531, http://www.ebi.ac.uk/efo/EFO_0004340 GCST002827 Genome-wide genotyping array 2015-12-03 25802187 Jiang DK 2015-04-28 Hepatology www.ncbi.nlm.nih.gov/pubmed/25802187 Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B. Chronic hepatitis B infection 2,514 Chinese ancestry cases, 1,130 Chinese ancestry controls 6,600 Chinese ancestry cases, 8,127 Chinese ancestry controls Illumina [3680900] (imputed) 12 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST002879 Genome-wide genotyping array 2016-01-30 25866641 Xu W 2015-03-19 Biomark Res www.ncbi.nlm.nih.gov/pubmed/25866641 A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. Survival in microsatellite instability low/stable colorectal cancer 431 European ancestry cases NA Illumina [729737] 12 disease free survival, microsatellite instability measurement, colorectal cancer, overall survival http://www.ebi.ac.uk/efo/EFO_0000409, http://www.ebi.ac.uk/efo/EFO_0007054, http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0000638 GCST002820 Genome-wide genotyping array 2016-01-30 25866641 Xu W 2015-03-19 Biomark Res www.ncbi.nlm.nih.gov/pubmed/25866641 A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. Survival in colon cancer 334 European ancestry cases NA Illumina [729737] 12 disease free survival, colonic neoplasm, overall survival http://www.ebi.ac.uk/efo/EFO_0000409, http://www.ebi.ac.uk/efo/EFO_0004288, http://www.ebi.ac.uk/efo/EFO_0000638 GCST002822 Genome-wide genotyping array 2016-01-30 25866641 Xu W 2015-03-19 Biomark Res www.ncbi.nlm.nih.gov/pubmed/25866641 A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes. Survival in rectal cancer 171 European ancestry cases NA Illumina [729737] 18 disease free survival, rectum cancer, overall survival http://www.ebi.ac.uk/efo/EFO_0000409, http://www.ebi.ac.uk/efo/EFO_1000657, http://www.ebi.ac.uk/efo/EFO_0000638 GCST002821 Genome-wide genotyping array 2016-01-30 25827949 Kunz M 2015-05-04 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/25827949 Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus. Cutaneous lupus erythematosus 151 European ancestry cases, 1,288 European ancestry controls 219 European ancestry cases, 262 European ancestry controls Affymetrix [906600] 7 cutaneous lupus erythematosus http://www.ebi.ac.uk/efo/EFO_0003834 GCST002884 Genome-wide genotyping array 2016-01-22 25799145 Kappen JH 2015-03-23 PLoS One www.ncbi.nlm.nih.gov/pubmed/25799145 Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease. Behcet's disease 1 Afghanistan ancestry case, 154 Middle Eastern/North African ancestry cases, 2 Cape Verdian cases, 1 Curacao case, 1 Dominican Republic ancestry cases, 54 European ancestry cases, 1 Israeli case, 1 Surinamese ancestry case, 1 Thai ancestry case, 1 Chinese ancestry case, 119 Turkish ancestry cases, 87 Middle Eastern/North African ancestry controls, 5,756 controls 82 European ancestry cases, 98 European ancestry controls Illumina [505454] 0 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST002823 Genome-wide genotyping array 2016-01-22 25799145 Kappen JH 2015-03-23 PLoS One www.ncbi.nlm.nih.gov/pubmed/25799145 Genome-wide association study in an admixed case series reveals IL12A as a new candidate in Behçet disease. Behcet's disease 1 Afghanistan ancestry case, 154 Middle Eastern/North African ancestry cases, 2 Cape Verdian cases, 1 Curacao case, 1 Dominican Republic ancestry cases, 54 European ancestry cases, 1 Israeli case, 1 Surinamese ancestry case, 1 Thai ancestry case, 1 Chinese ancestry case, 119 Turkish ancestry cases, 87 Middle Eastern/North African ancestry controls, 5,756 controls 2,030 Turkish cases, 1,904 Turkish controls Illumina [505454] 1 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST002824 Genome-wide genotyping array 2015-11-21 25855136 Stacey SN 2015-04-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25855136 New basal cell carcinoma susceptibility loci. Basal cell carcinoma 4,572 European ancestry cases, 266,358 European ancestry controls up to 956 European ancestry cases, up to 4,214 European ancestry controls, 526 cases, 528 controls Illumina [24988228] (imputed) 13 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST002842 Genome-wide genotyping array 2016-02-04 25862617 Zhang Y 2015-04-10 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/25862617 Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations. Systemic lupus erythematosus 1,656 Chinese ancestry cases, 3,394 Chinese ancestry controls 2,152 Chinese ancestry cases, 2,476 Chinese ancestry controls, 460 Thai ancestry cases, 965 Thai ancestry controls Illumina [up to 493645] 1 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST002845 Genome-wide genotyping array 2016-02-10 25903422 Yin X 2015-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25903422 Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Psoriasis 3,496 European ancestry cases, 5,186 European ancestry controls, 1,588 Chinese ancestry cases, 3,546 Chinese ancestry controls 5,134 European ancestry cases, 5,633 European ancestry controls, 5,151 Chinese ancestry cases, 5,152 Chinese ancestry controls Illumina [up to 4778154] (imputed) 68 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST002874 Genome-wide genotyping array 2015-12-09 25644374 Poirier JG 2015-01-19 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25644374 Informed genome-wide association analysis with family history as a secondary phenotype identifies novel loci of lung cancer. Lung cancer and family history of lung cancer 3,953 European ancestry lung cancer cases, 4,730 European ancestry lung cancer controls NA Illumina [317924] 0 lung carcinoma, family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0006953 GCST002753 Genome-wide genotyping array 2015-12-18 25637523 Springelkamp H 2015-01-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25637523 ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure. Intraocular pressure 8,015 individuals 7,471 individuals Illumina [NR] (imputed) 48 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST002767 Genome-wide genotyping array 2015-11-25 25813999 Jeong S 2015-04-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/25813999 Identification of a Novel Mucin Gene HCG22 Associated With Steroid-Induced Ocular Hypertension. Change in intraocular pressure in response to steroid treatment (triamcinolone acetonide) 64 European ancestry individuals 49 European ancestry individuals Illumina [1545328] 1 response to triamcinolone acetonide, intraocular pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006954, http://www.ebi.ac.uk/efo/EFO_0006956 GCST002837 Genome-wide genotyping array 2016-02-04 25673412 Shungin D 2015-02-12 Nature www.ncbi.nlm.nih.gov/pubmed/25673412 New genetic loci link adipose and insulin biology to body fat distribution. Waist-to-hip ratio adjusted for body mass index up to 56,910 European ancestry men, up to 86,570 European ancestry women up to 36,570 European ancestry men, 30,172 European ancestry women, 915 Filipino ancestry men, 735 Filipino ancestry women, 2,351 African American/Afro-Caribbean ancestry men, 6,258 African American/Afro-Caribbean ancestry women, 2,285 South Asian ancestry men, 506 South Asian ancestry women, 195 Seychellois ancestry men, 266 Seychellois ancestry women Affymetrix, Illumina, Perlegen [up to 2542447] (imputed) 286 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST002782 Genome-wide genotyping array 2017-05-23 25673412 Shungin D 2015-02-12 Nature www.ncbi.nlm.nih.gov/pubmed/25673412 New genetic loci link adipose and insulin biology to body fat distribution. Waist-hip ratio up to 56,910 European ancestry men, up to 86,570 European ancestry women up to 36,570 European ancestry men, 30,172 European ancestry women, 915 Filipino ancestry men, 735 Filipino ancestry women, 2,351 African American/Afro-Caribbean ancestry men, 6,258 African American/Afro-Caribbean ancestry women, 2,285 South Asian ancestry men, 506 South Asian ancestry women, 195 Seychellois ancestry men, 266 Seychellois ancestry women Affymetrix, Illumina, Perlegen [up to 2542447] (imputed) 78 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST004064 Genome-wide genotyping array 2017-05-23 25673412 Shungin D 2015-02-12 Nature www.ncbi.nlm.nih.gov/pubmed/25673412 New genetic loci link adipose and insulin biology to body fat distribution. Waist circumference up to 56,910 European ancestry men, up to 86,570 European ancestry women up to 36,570 European ancestry men, 30,172 European ancestry women, 915 Filipino ancestry men, 735 Filipino ancestry women, 2,351 African American/Afro-Caribbean ancestry men, 6,258 African American/Afro-Caribbean ancestry women, 2,285 South Asian ancestry men, 506 South Asian ancestry women, 195 Seychellois ancestry men, 266 Seychellois ancestry women Affymetrix, Illumina, Perlegen [up to 2542447] (imputed) 106 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST004065 Genome-wide genotyping array 2017-05-23 25673412 Shungin D 2015-02-12 Nature www.ncbi.nlm.nih.gov/pubmed/25673412 New genetic loci link adipose and insulin biology to body fat distribution. Hip circumference adjusted for BMI up to 56,910 European ancestry men, up to 86,570 European ancestry women up to 36,570 European ancestry men, 30,172 European ancestry women, 915 Filipino ancestry men, 735 Filipino ancestry women, 2,351 African American/Afro-Caribbean ancestry men, 6,258 African American/Afro-Caribbean ancestry women, 2,285 South Asian ancestry men, 506 South Asian ancestry women, 195 Seychellois ancestry men, 266 Seychellois ancestry women Affymetrix, Illumina, Perlegen [up to 2542447] (imputed) 225 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST004067 Genome-wide genotyping array 2017-05-23 25673412 Shungin D 2015-02-12 Nature www.ncbi.nlm.nih.gov/pubmed/25673412 New genetic loci link adipose and insulin biology to body fat distribution. Waist circumference adjusted for body mass index up to 56,910 European ancestry men, up to 86,570 European ancestry women up to 36,570 European ancestry men, 30,172 European ancestry women, 915 Filipino ancestry men, 735 Filipino ancestry women, 2,351 African American/Afro-Caribbean ancestry men, 6,258 African American/Afro-Caribbean ancestry women, 2,285 South Asian ancestry men, 506 South Asian ancestry women, 195 Seychellois ancestry men, 266 Seychellois ancestry women Affymetrix, Illumina, Perlegen [up to 2542447] (imputed) 169 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST004063 Genome-wide genotyping array 2017-05-23 25673412 Shungin D 2015-02-12 Nature www.ncbi.nlm.nih.gov/pubmed/25673412 New genetic loci link adipose and insulin biology to body fat distribution. Hip circumference up to 56,910 European ancestry men, up to 86,570 European ancestry women up to 36,570 European ancestry men, 30,172 European ancestry women, 915 Filipino ancestry men, 735 Filipino ancestry women, 2,351 African American/Afro-Caribbean ancestry men, 6,258 African American/Afro-Caribbean ancestry women, 2,285 South Asian ancestry men, 506 South Asian ancestry women, 195 Seychellois ancestry men, 266 Seychellois ancestry women Affymetrix, Illumina, Perlegen [up to 2542447] (imputed) 142 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST004066 Genome-wide genotyping array 2015-11-08 25644384 Davies G 2015-02-03 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25644384 Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53949). Cognitive function 51,719 European ancestry individuals, 1,473 Erasmus Rucphen (founder/genetic isolate) individuals, 327 Korculan (founder/genetic isolate) individuals, 430 Orcadian (founder/genetic isolate) individuals NA Affymetrix, Illumina [2478500] (imputed) 34 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST002774 Genome-wide genotyping array 2015-12-16 25672763 Ueta M 2015-02-08 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/25672763 IKZF1, a new susceptibility gene for cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis with severe mucosal involvement. Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe mucosal involvement 117 Japanese ancestry cases, 691 Japanese ancestry controls 43 East Asian ancestry cases, 278 East Asian ancestry controls, 20 Indian ancestry cases, 56 Indian ancestry controls, 39 Brazilian ancestry cases, 135 Brazilian ancestry controls Affymetrix [449205] 1 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to cold medicine http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://www.ebi.ac.uk/efo/EFO_0006997 GCST002779 Genome-wide genotyping array 2014-07-28 24322204 Winham SJ 2013-12-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24322204 Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2. Bipolar disorder (body mass index interaction) 388 European ancestry cases, 1,020 European ancestry controls NA NR [up to 8466825] (imputed) 51 bipolar disorder, body mass index http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0004340 GCST002306 Genome-wide genotyping array 2015-04-01 25023989 Schmit SL 2014-07-14 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/25023989 A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study. Colorectal cancer 485 Ashkenazi Jewish cases, 498 Ashkenazi Jewish controls, 1,977 European ancestry cases, 999 European ancestry controls 1,131 Ashkenazi Jewish cases, 831 Ashkenazi Jewish controls Illumina [up to 9177523] (imputed) 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002528 Genome-wide genotyping array 2015-05-07 25208829 Anderson D 2014-09-11 Genes Immun www.ncbi.nlm.nih.gov/pubmed/25208829 Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study. Vitamin D levels 645 European ancestry age 6 individuals, 28 age 6 individuals, 1,073 European ancestry age 14 individuals, 67 age 14 individuals NA Illumina [2461244] (imputed) 11 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST002602 Genome-wide genotyping array 2015-09-22 25475840 Colodro-Conde L 2014-12-05 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/25475840 A twin study of breastfeeding with a preliminary genome-wide association scan. Breastfeeding duration 1,521 mothers from 1,073 families NA Illumina [6590000] (imputed) 9 breastfeeding duration http://www.ebi.ac.uk/efo/EFO_0006864 GCST002715 Genome-wide genotyping array 2014-10-21 24614497 Oikkonen J 2014-03-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24614497 A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions. Musical aptitude 767 European ancestry individuals from 76 families NA Illumina [664177] 0 musical aptitude http://www.ebi.ac.uk/efo/EFO_0005690 GCST002387 Genome-wide genotyping array 2015-07-17 24931836 Diekstra FP 2014-06-27 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/24931836 C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis. Amyotrophic lateral sclerosis or frontotemporal dementia 4,377 European ancestry ALS cases, 435 European ancestry FTD cases, 14,431 European ancestry controls 4,056 European ancestry ALS cases, 3,958 European ancestry controls Illumina [~ 1400000] (imputed) 1 frontotemporal dementia, amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0017276, http://purl.obolibrary.org/obo/MONDO_0004976 GCST002510 Genome-wide genotyping array 2015-07-17 24931836 Diekstra FP 2014-06-27 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/24931836 C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis. Frontotemporal dementia 435 European ancestry cases, 1,414 European ancestry controls NA Illumina [~ 1400000] (imputed) 1 frontotemporal dementia http://purl.obolibrary.org/obo/MONDO_0017276 GCST002508 Genome-wide genotyping array 2015-09-22 24931836 Diekstra FP 2014-06-27 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/24931836 C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis. Amyotrophic lateral sclerosis 4,377 European ancestry cases, 13,017 European ancestry controls NA Illumina [~ 1400000] (imputed) 6 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST002509 Genome-wide genotyping array 2012-02-22 22291609 Naitza S 2012-01-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/22291609 A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation. Inflammatory biomarkers 4,694 Sardinian individuals 1,392 Sardinian individuals Affymetrix [~ 1900000] (imputed) 7 blood sedimentation, interleukin-6 measurement, C-reactive protein measurement, CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004304, http://www.ebi.ac.uk/efo/EFO_0004810, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0004749 GCST001385 Genome-wide genotyping array 2014-10-22 24618891 Muhleisen TW 2014-03-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24618891 Genome-wide association study reveals two new risk loci for bipolar disorder. Bipolar disorder 9,747 European ancestry cases, 14,278 European ancestry controls NA Illumina [2267487] (imputed) 6 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST002385 Genome-wide genotyping array 2015-05-27 25266886 Kim JJ 2014-09-30 Pediatr Cardiol www.ncbi.nlm.nih.gov/pubmed/25266886 Common variants in the CRP promoter are associated with a high C-reactive protein level in Kawasaki disease. Inflammatory biomarkers in Kawasaki disease 178 Korean ancestry cases 473 Korean ancestry cases Illumina [646914] 1 inflammatory biomarker measurement, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004872, http://www.ebi.ac.uk/efo/EFO_0004458 GCST002640 Genome-wide genotyping array 2014-10-20 24503447 Nelson D 2014-02-06 Antivir Ther www.ncbi.nlm.nih.gov/pubmed/24503447 Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor. Response to protease inhibitor treatment in hepatitis c (bilirubin toxicity) 176 European ancestry individuals NA Illumina [4466593] 3 response to protease inhibitor http://www.ebi.ac.uk/efo/EFO_0005657 GCST002347 Genome-wide genotyping array 2014-10-20 24503447 Nelson D 2014-02-06 Antivir Ther www.ncbi.nlm.nih.gov/pubmed/24503447 Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor. Response to protease inhibitor treatment in hepatitis c (peak serum total bilirubin levels) 176 European ancestry individuals NA Illumina [4466593] 4 response to protease inhibitor http://www.ebi.ac.uk/efo/EFO_0005657 GCST002349 Genome-wide genotyping array 2014-10-22 24586183 Medici M 2014-02-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24586183 Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease. Thyroid peroxidase antibody positivity 1,769 European ancestry cases, 16,528 European ancestry controls 922 European ancestry cases, 8,068 European ancestry controls Affymetrix, Illumina [up to 3437411] (imputed) 9 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST002378 Genome-wide genotyping array 2014-10-22 24586183 Medici M 2014-02-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24586183 Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease. Thyroid peroxidase antibody levels 12,353 European ancestry individuals 8,159 European ancestry individuals Affymetrix, Illumina [up to 3437411] (imputed) 5 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST002373 Genome-wide genotyping array 2014-03-18 23989986 Evangelou E 2013-08-29 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/23989986 A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip. Osteoarthritis (hip) up to 4,734 European ancestry cases, up to 46,903 European ancestry controls up to 6,928 European ancestry cases, up to 20,570 European ancestry controls Illumina [2567279] (imputed) 5 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST002155 Genome-wide genotyping array 2015-07-07 25372704 Mtatiro SN 2014-11-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/25372704 Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania. Fetal hemoglobin levels in sickle cell anemia 1,213 Tanzanian ancestry cases 321 Afro-Caribbean and Sub-Saharan African cases Illumina [15153765] (imputed) 2 fetal hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004576 GCST002687 Genome-wide genotyping array 2015-08-09 25503805 Karnes JH 2014-12-11 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/25503805 A genome-wide association study of heparin-induced thrombocytopenia using an electronic medical record. Heparin-induced thrombocytopenia 57 European ancestry cases, 8 African American cases, 1 other ancestry cases, 1 case, 754 European ancestry controls, 108 African American controls, 6 other ancestry controls, 6 controls, 8 Hispanic controls, 1 Asian control 94 European ancestry cases, 178 European ancestry antibody positive controls, 154 European ancestry antibody negative controls Illumina [7604479] (imputed) 0 response to heparin, Thrombocytopenia http://www.ebi.ac.uk/efo/EFO_0006816, http://purl.obolibrary.org/obo/HP_0001873 GCST002722 Genome-wide genotyping array 2015-06-07 25303641 Zhang F 2014-09-25 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/25303641 Genome-wide association study identifies ITPR2 as a susceptibility gene for Kashin-Beck disease in Han Chinese. Kashin-Beck disease 90 Han Chinese ancestry cases, 1,627 Han Chinese ancestry controls 559 Han Chinese ancestry cases, 467 Han Chinese ancestry controls Affymetrix [532894] 1 Kashin-Beck disease http://www.ebi.ac.uk/efo/EFO_0006511 GCST002634 Genome-wide genotyping array 2015-09-14 25493955 Gorski M 2014-12-10 Kidney Int www.ncbi.nlm.nih.gov/pubmed/25493955 Genome-wide association study of kidney function decline in individuals of European descent. Kidney function decline traits up to 45,530 European ancestry individuals up to 18,028 European ancestry individuals Affymetrix, Illumina [2500000] (imputed) 8 chronic kidney disease, rapid kidney function decline, GFR change measurement http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0006836, http://www.ebi.ac.uk/efo/EFO_0006829 GCST002720 Genome-wide genotyping array 2015-01-20 24925725 Chung SA 2014-06-12 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/24925725 Lupus nephritis susceptibility loci in women with systemic lupus erythematosus. Lupus nephritis in systemic lupus erythematosus 588 European ancestry cases, 1,412 European ancestry controls NA Affymetrix, Illumina [1621689] (imputed) 17 lupus nephritis http://www.ebi.ac.uk/efo/EFO_0005761 GCST002479 Genome-wide genotyping array 2014-11-08 24700089 Miura K 2014-04-04 J Med Virol www.ncbi.nlm.nih.gov/pubmed/24700089 Genome-wide association study of HPV-associated cervical cancer in Japanese women. Cervical cancer 226 Japanese ancestry cases, 186 Japanese ancestry controls NA Affymetrix [556045] 9 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST002405 Genome-wide genotyping array 2013-05-01 23372041 Chu AY 2013-01-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/23372041 Novel locus including FGF21 is associated with dietary macronutrient intake. Dietary macronutrient intake 33,533 European ancestry individuuals 38,360 European ancestry individuuals Affymetrix, Illumina [~ 2600000] (imputed) 3 energy intake http://www.ebi.ac.uk/efo/EFO_0003939 GCST001844 Genome-wide genotyping array 2013-05-14 23392654 Lewis JP 2013-02-07 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/23392654 Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes. Response to antiplatelet therapy 565 European ancestry individuals 710 European ancestry individuals, 237 African American individuals, 276 Hispanic individuals, 4 individuals Affymetrix [400230] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST001855 Genome-wide genotyping array 2014-08-05 24390342 Okada Y 2013-12-25 Nature www.ncbi.nlm.nih.gov/pubmed/24390342 Genetics of rheumatoid arthritis contributes to biology and drug discovery. Rheumatoid arthritis up to 14,361 European ancestry cases, up to 42,923 European ancestry controls, up to 4,873 East Asian ancestry cases, up to 17,642 East Asian ancestry controls up to 3,775 European ancestry cases, up to 5,801 European ancestry controls, up to 6,871 East Asian ancestry cases, up to 6,392 East Asian ancestry controls Affymetrix, Illumina [up to 9739303] (imputed) 181 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST002318 Genome-wide genotyping array 2015-06-20 25340798 Kauwe JS 2014-10-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25340798 Genome-wide association study of CSF levels of 59 alzheimer's disease candidate proteins: significant associations with proteins involved in amyloid processing and inflammation. Cerebrospinal fluid levels of Alzheimer's disease-related proteins 574 individuals NA Illumina [5815690] (imputed) 5 matrix metalloproteinase measurement, angiotensin-converting enzyme measurement, Alzheimer disease, CCL4 measurement, interleukin-6 measurement, Alzheimer's disease biomarker measurement, CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004744, http://www.ebi.ac.uk/efo/EFO_0006515, http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004751, http://www.ebi.ac.uk/efo/EFO_0004810, http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004749 GCST002665 Genome-wide genotyping array 2014-11-26 24871463 Armstrong DL 2014-05-29 Genes Immun www.ncbi.nlm.nih.gov/pubmed/24871463 GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region. Systemic lupus erythematosus 725 European ancestry cases, 2,438 European ancestry controls NA Illumina [NR] 25 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST002463 Genome-wide genotyping array 2014-12-16 24938310 Nakano M 2014-06-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/24938310 Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population. Exfoliation glaucoma or exfoliation syndrome 201 Japanese ancestry cases, 697 Japanese ancestry controls 121 Japanese ancestry cases, 263 Japanese ancestry controls Affymetrix [652792] 2 exfoliation syndrome http://www.ebi.ac.uk/efo/EFO_0004235 GCST002486 Genome-wide genotyping array 2013-03-05 23233654 Umicevic Mirkov M 2012-12-11 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/23233654 Genome-wide association analysis of anti-TNF drug response in patients with rheumatoid arthritis. Response to TNF-alpha inhibitors in rheumatoid arthritis 882 European ancestry cases 1,821 European ancestry cases Illumina [2450096] (imputed) 0 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST001772 Genome-wide genotyping array 2013-03-15 23233662 Ramsey LB 2012-12-11 Blood www.ncbi.nlm.nih.gov/pubmed/23233662 Genome-wide study of methotrexate clearance replicates SLCO1B1. Methotrexate clearance (acute lymphoblastic leukemia) 22 East Asian ancestry cases, 58 African ancestry, African American or Afro-Caribbean cases, 266 Hispanic or Latin American cases, 806 European ancestry cases, 127 cases 699 European ancestry cases Affymetrix [~ 5200000] (imputed) 1 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST001770 Genome-wide genotyping array 2015-05-09 25064009 Nalls MA 2014-07-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25064009 Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. Parkinson's disease 13,708 European ancestry cases, 95,282 European ancestry controls 5,353 European ancestry cases, 5,551 European ancestry controls Illumina [7893274] (imputed) 26 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST002544 Genome-wide genotyping array 2014-07-25 24280104 Wu AC 2013-11-23 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/24280104 Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics. Bronchodilator response in asthma (inhaled corticosteroid treatment interaction) 172 European ancestry cases, 409 European ancestry controls 227 European ancestry cases Illumina [449540] 5 response to bronchodilator, response to corticosteroid http://purl.obolibrary.org/obo/GO_0097366, http://purl.obolibrary.org/obo/GO_0031960 GCST002291 Genome-wide genotyping array 2014-11-19 24811271 Kennedy RB 2014-05-09 Immunogenetics www.ncbi.nlm.nih.gov/pubmed/24811271 Genome-wide SNP associations with rubella-specific cytokine responses in measles-mumps-rubella vaccine recipients. Immune response to measles-mumps-rubella vaccine 883 European ancestry individuals NA Illumina [NR] 11 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST002441 Genome-wide genotyping array 2013-09-18 23555189 Chen Z 2013-04-01 Neoplasia www.ncbi.nlm.nih.gov/pubmed/23555189 Genome-wide association study identifies genetic determinants of urine PCA3 levels in men. PCA3 expression level 1,371 European ancestry individuals NA Illumina [3076666] (imputed) 4 cancer biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005127 GCST001946 Genome-wide genotyping array 2014-08-02 24390345 Williams AL 2013-12-25 Nature www.ncbi.nlm.nih.gov/pubmed/24390345 Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico. Type 2 diabetes 3,848 Mexican and other Latin American ancestry cases, 4,366 Mexican and other Latin American ancestry controls 896 Mexican American cases, 832 Mexican American controls, 2,768 East Asian ancestry cases, 2,880 East Asian ancestry controls, 1,082 South Asian ancestry cases, 1,105 South Asian ancestry controls, 1,874 European ancestry cases, 1,333 European ancestry controls, 2,127 African American cases, 2,103 African American controls, 698 Native Hawaiian ancestry cases, 579 Native Hawaiian ancestry controls, 2,009 Singaporean ancestry cases, 1959 Singaporean ancestry controls Illumina [9200000] (imputed) 4 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002317 Genome-wide genotyping array 2009-09-28 17434869 Frayling TM 2007-04-12 Science www.ncbi.nlm.nih.gov/pubmed/17434869 A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Body mass index 5,483 European ancestry type 2 diabetes cases, 5,174 European ancestry controls 19,424 European ancestry adult individuals, 10,172 European ancestry children Affymetrix [490032] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000022 Genome-wide genotyping array 2015-05-21 25364816 Awata T 2014-11-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/25364816 A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA. Diabetic retinopathy in type 2 diabetes 205 Japanese ancestry cases, 241 Japanese ancestry controls 632 Japanese ancestry cases, 908 Japanese ancestry controls Affymetrix [614216] 1 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST002684 Genome-wide genotyping array 2012-12-21 23031429 Surakka I 2012-10-03 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/23031429 A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Apolipoprotein Levels 1,720 European ancestry monozygotic twins NA Illumina [~ 2500000] (imputed) 3 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST001703 Genome-wide genotyping array 2012-12-21 23031429 Surakka I 2012-10-03 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/23031429 A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol. Cholesterol and Triglycerides 1,720 European ancestry monozygotic twins 1,261 European ancestry monozygotic twins Illumina [~ 2500000] (imputed) 1 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST001704 Genome-wide genotyping array 2014-07-25 24281739 Boardman JD 2013-11-27 Demography www.ncbi.nlm.nih.gov/pubmed/24281739 Is the gene-environment interaction paradigm relevant to genome-wide studies? The case of education and body mass index. Body mass index (education interaction) 816 non-college graduate individuals, 1,061 college graduate individuals NA Affymetrix [260402] 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002296 Genome-wide genotyping array 2009-09-28 17470457 Huentelman MJ 2007-04-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/17470457 Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance. Episodic memory 341 European ancestry individuals 472 European ancestry individuals Affymetrix [~ 502627] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST000029 Genome-wide genotyping array 2010-03-02 20125088 Shi J 2010-02-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20125088 Genome-wide association study of recurrent early-onset major depressive disorder. Major depressive disorder 1,020 European ancestry cases, 1,636 European ancestry controls NA Affymetrix [671424] 9 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST000578 Genome-wide genotyping array 2009-09-28 17846126 Rampersaud E 2007-09-10 Diabetes www.ncbi.nlm.nih.gov/pubmed/17846126 Identification of novel candidate genes for type 2 diabetes from a genome-wide association scan in the Old Order Amish: evidence for replication from diabetes-related quantitative traits and from independent populations. Type 2 diabetes 124 Old Order Amish cases, 295 Old Order Amish controls 1,555 European ancestry cases, 1,467 European ancestry controls, 300 Pima Indian ancestry cases, 334 Pima Indian ancestry controls, 287 Mexican American cases, 316 Mexican American controls Affymetrix [82485] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000076 Genome-wide genotyping array 2014-05-01 24094242 Li J 2013-10-05 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/24094242 Genome-wide association study on serum alkaline phosphatase levels in a Chinese population. Serum alkaline phosphatase levels 1,452 Han Chinese ancestry individuals 8,830 Han Chinese ancestry individuals Affymetrix [658288] 4 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST002214 Genome-wide genotyping array 2014-07-22 24265751 Li W 2013-11-12 PLoS One www.ncbi.nlm.nih.gov/pubmed/24265751 DNA pooling base genome-wide association study identifies variants at NRXN3 associated with delayed encephalopathy after acute carbon monoxide poisoning. Delayed encephalopathy in acute carbon monoxide poisoning 175 Han Chinese ancestry cases, 244 Han Chinese ancestry controls 234 Han Chinese ancestry cases, 271 Han Chinese ancestry controls Illumina [NR] 0 delayed encephalopathy after acute carbon monoxide poisoning http://www.ebi.ac.uk/efo/EFO_0005534 GCST002271 Genome-wide genotyping array 2014-11-19 24816038 Postmus I 2014-04-26 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/24816038 In search for genetic determinants of clinically meaningful differential cardiovascular event reduction by pravastatin in the PHArmacogenetic study of Statins in the Elderly at risk (PHASE)/PROSPER study. Cardiovascular event reduction in the elderly at risk for vascular disease (statin therapy interaction) 5,244 individuals 1,233 cases Illumina [2500000] (imputed) 0 response to statin http://purl.obolibrary.org/obo/GO_0036273 GCST002428 Genome-wide genotyping array 2015-05-07 22533364 Yashin AI 2012-04-25 Rejuvenation Res www.ncbi.nlm.nih.gov/pubmed/22533364 Polygenic effects of common single-nucleotide polymorphisms on life span: when association meets causality. Longevity 1,173 individuals NA Affymetrix [550000] 0 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST001492 Genome-wide genotyping array 2014-03-21 23989729 Feenstra B 2013-08-21 JAMA www.ncbi.nlm.nih.gov/pubmed/23989729 Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis. Infantile hypertrophic pyloric stenosis 1,001 European ancestry cases, 2,371 European ancestry controls 925 European ancestry cases, 1,621 European ancestry controls, 738 cases, 697 controls Illumina [9737928] (imputed) 4 infantile hypertrophic pyloric stenosis http://www.ebi.ac.uk/efo/EFO_0004707 GCST002145 Genome-wide genotyping array 2014-10-28 24571439 Nudel R 2014-02-26 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24571439 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Parent of origin effect on language impairment (paternal) 153 European ancestry case-parent trios, 54 European ancestry case-mother duos, 12 European ancestry case-father duos, 18 European ancestry cases NA Illumina [614937] 4 language impairment http://www.ebi.ac.uk/efo/EFO_0005425 GCST002371 Genome-wide genotyping array 2014-10-28 24571439 Nudel R 2014-02-26 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24571439 Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment. Parent of origin effect on language impairment (maternal) 153 European ancestry case-parent trios, 54 European ancestry case-mother duos, 12 European ancestry case-father duos, 18 European ancestry cases 193 European ancestry case-mother duos, 75 European ancestry cases, 45 European ancestry mothers of cases Illumina [614937] 0 language impairment http://www.ebi.ac.uk/efo/EFO_0005425 GCST002369 Genome-wide genotyping array 2014-04-02 24024963 Eicher JD 2013-09-11 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24024963 Genome-wide association study of shared components of reading disability and language impairment. Reading disability and language impairment 174 European ancestry cases, 4,117 European ancestry controls 440 European ancestry individuals Illumina [up to 500527] 0 language impairment, dyslexia http://www.ebi.ac.uk/efo/EFO_0005425, http://www.ebi.ac.uk/efo/EFO_0005424 GCST002175 Genome-wide genotyping array 2014-10-28 24569950 Hatemi PK 2014-02-26 Behav Genet www.ncbi.nlm.nih.gov/pubmed/24569950 Genetic influences on political ideologies: twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations. Political ideology 11,388 European ancestry individuals from 6,758 families NA Illumina [> 269840] (imputed) 19 economic and social preference http://www.ebi.ac.uk/efo/EFO_0004827 GCST002372 Genome-wide genotyping array 2014-12-18 24945404 Kemp JP 2014-06-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24945404 Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment. Bone mineral density (paediatric, upper limb) 8,007 European ancestry children, 289 Surinamese ancestry children, 300 Turkish ancestry children, 232 Moroccan ancestry children, 588 children NA Illumina [~ 2500000] (imputed) 11 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST002496 Genome-wide genotyping array 2014-12-18 24945404 Kemp JP 2014-06-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24945404 Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment. Bone mineral density (paediatric, total body less head) 8,007 European ancestry children, 289 Surinamese ancestry children, 300 Turkish ancestry children, 232 Moroccan ancestry children, 588 children NA Illumina [~ 2500000] (imputed) 15 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST002494 Genome-wide genotyping array 2014-12-18 24945404 Kemp JP 2014-06-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24945404 Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment. Bone mineral density (paediatric, lower limb) 8,007 European ancestry children, 289 Surinamese ancestry children, 300 Turkish ancestry children, 232 Moroccan ancestry children, 588 children NA Illumina [~ 2500000] (imputed) 11 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST002492 Genome-wide genotyping array 2014-12-18 24945404 Kemp JP 2014-06-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24945404 Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment. Bone mineral density (paediatric, skull) 7,976 European ancestry children, 289 Surinamese ancestry children, 300 Turkish ancestry children, 232 Moroccan ancestry children, 588 children NA Illumina [~ 2500000] (imputed) 19 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST002493 Genome-wide genotyping array 2012-11-02 22941191 Diskin SJ 2012-09-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22941191 Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma. Neuroblastoma 2,101 European ancestry cases, 4,202 European ancestry controls 351 European ancestry cases, 780 European ancestry controls, 365 African American cases, 2,491 African American controls Illumina [426697] 6 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST001660 Genome-wide genotyping array 2014-02-13 23150908 Jonsson T 2012-11-14 N Engl J Med www.ncbi.nlm.nih.gov/pubmed/23150908 Variant of TREM2 associated with the risk of Alzheimer's disease. Alzheimer's disease 3,550 European ancestry cases, 8,888 European ancestry controls 694 European ancestry cases, 4,375 European ancestry controls, 1,343 cases, 5,352 controls NR [NR] 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001743 Genome-wide genotyping array 2014-10-01 23644456 Styrkarsdottir U 2013-05-05 Nature www.ncbi.nlm.nih.gov/pubmed/23644456 Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits. Bone mineral density 4,931 European ancestry cases, 69,034 European ancestry controls NA Illumina [30600000] (imputed) 2 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST002011 Genome-wide genotyping array 2014-04-05 24084763 Wang J 2013-10-01 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/24084763 Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study. Colorectal adenoma (advanced) 139 European ancestry cases, 1,267 European ancestry controls 4,175 European ancestry cases, 5,036 European ancestry controls Illumina [NR] 0 colorectal adenoma http://www.ebi.ac.uk/efo/EFO_0005406 GCST002212 Genome-wide genotyping array 2015-05-08 25201988 Rietveld CA 2014-09-08 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/25201988 Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Educational attainment 106,736 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 68 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST002598 Genome-wide genotyping array 2015-06-22 25192705 Du M 2014-09-05 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/25192705 No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk. Colorectal cancer (calcium intake interaction) 9,006 European ancestry cases, 9,503 European ancestry controls NA NR [~ 2700000] (imputed) 3 calcium intake measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0006521, http://purl.obolibrary.org/obo/MONDO_0005575 GCST002596 Genome-wide genotyping array 2013-02-13 23180869 Wu C 2012-11-24 Gut www.ncbi.nlm.nih.gov/pubmed/23180869 Genome-wide association study of survival in patients with pancreatic adenocarcinoma. Pancreatic cancer 642 European ancestry cases 363 Chinese ancestry cases Illumina [2731086] (imputed) 7 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST001749 Genome-wide genotyping array 2013-01-22 23047291 Brown CC 2012-11-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/23047291 A genome-wide association analysis of temozolomide response using lymphoblastoid cell lines shows a clinically relevant association with MGMT. Response to temozolomide 516 European ancestry lymphoblastoid cell lines NA Illumina [2074734] (imputed) 1 response to temozolomide http://purl.obolibrary.org/obo/GO_1990054 GCST001730 Genome-wide genotyping array 2014-03-22 24023261 Keller M 2013-09-10 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/24023261 THOC5: a novel gene involved in HDL-cholesterol metabolism. Lipid traits 839 European ancestry individuals up to 5,248 European ancestry individuals Affymetrix [390619] 6 triglyceride measurement, low density lipoprotein cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004612 GCST002173 Genome-wide genotyping array 2013-02-06 23183192 Deo R 2012-11-23 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/23183192 Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants. Resting heart rate 13,372 African American individuals Affymetrix, Illumina [2954965] (imputed) 2 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST001748 Genome-wide genotyping array 2009-12-29 20031578 Pare G 2009-04-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031578 Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study. Homocysteine levels 13,974 European ancestry females 840 European ancestry females Illumina [336469] 2 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST000367 Genome-wide genotyping array 2009-12-29 20031564 Ridker PM 2009-02-01 Circ Cardiovasc Genet www.ncbi.nlm.nih.gov/pubmed/20031564 Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study. HDL cholesterol 18,245 European ancestry females NA Illumina [~ 318237] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST000331 Genome-wide genotyping array 2011-09-13 21810643 Bakken TE 2011-08-01 Arch Gen Psychiatry www.ncbi.nlm.nih.gov/pubmed/21810643 Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia. Cortical thickness 573 European ancestry cases, 481 European ancestry controls NA Affymetrix [597198] 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST001187 Genome-wide genotyping array 2013-02-28 23202124 Horikoshi M 2012-12-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23202124 New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism. Birth weight Up to 26,836 European ancestry individuals Up to 42,519 European ancestry individuals Affymetrix, Illumina [~ 2700000] (imputed) 10 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST001758 Genome-wide genotyping array 2012-12-06 23006423 Niu N 2012-09-24 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/23006423 Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study. Response to taxane treatment (placlitaxel) 96 African American lymphoblastoid cell lines, 96 European ancestry lymphoblastoid cell lines, 96 Han Chinese ancestry lymphoblastoid cell lines NA Affymetrix, Illumina [~ 1300000] 13 methylcobalamin deficiency type cblE http://purl.obolibrary.org/obo/MONDO_0009354 GCST001694 Genome-wide genotyping array 2012-12-06 23006423 Niu N 2012-09-24 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/23006423 Genetic association with overall survival of taxane-treated lung cancer patients - a genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study. Response to taxane treatment (docetaxel) 96 African American lymphoblastoid cell lines, 96 European ancestry lymphoblastoid cell lines, 96 Han Chinese ancestry lymphoblastoid cell lines NA Affymetrix, Illumina [~ 1300000] 16 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST001692 Genome-wide genotyping array 2014-10-10 24483146 Li L 2014-02-01 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/24483146 Discovery of genetic biomarkers contributing to variation in drug response of cytidine analogues using human lymphoblastoid cell lines. Response to cytidine analogues (gemcitabine) 60 European ancestry lymphoblastoid cell lines, 54 African American lymphoblastoid cell lines, 60 Han Chinese ancestry lymphoblastoid cell lines NA Affymetrix, Illumina [1348798] 10 response to gemcitabine http://purl.obolibrary.org/obo/GO_0036272 GCST002343 Genome-wide genotyping array 2014-10-10 24483146 Li L 2014-02-01 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/24483146 Discovery of genetic biomarkers contributing to variation in drug response of cytidine analogues using human lymphoblastoid cell lines. Response to cytadine analogues (cytosine arabinoside) 60 European ancestry lymphoblastoid cell lines, 54 African American lymphoblastoid cell lines, 60 Han Chinese ancestry lymphoblastoid cell lines NA Affymetrix, Illumina [1348798] 22 response to cytosine arabinoside http://www.ebi.ac.uk/efo/EFO_0005655 GCST002345 Genome-wide genotyping array 2013-03-06 23209447 Tang M 2012-11-29 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23209447 The principal genetic determinants for nasopharyngeal carcinoma in China involve the HLA class I antigen recognition groove. Nasopharyngeal carcinoma up to 1,405 Han Chinese ancestry cases, up to 2,650 Han Chinese ancestry controls 356 Han Chinese ancestry cases, 629 Han Chinese ancestry controls Affymetrix [591458] 6 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST001752 Genome-wide genotyping array 2009-09-28 18067574 Butcher LM 2008-01-22 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/18067574 Genome-wide quantitative trait locus association scan of general cognitive ability using pooled DNA and 500K single nucleotide polymorphism microarrays. General cognitive ability 458 European ancestry low General cognitive ability children, 402 European ancestry high General codnitive ability children 3,195 European ancestry children Affymetrix [449127] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST000145 Genome-wide genotyping array 2015-06-08 25350695 Postmus I 2014-10-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25350695 Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins. Response to statins (LDL cholesterol change) 18,596 European ancestry individuals 23,279 European ancestry individuals Affymetrix, Illumina, Perlegen [at least 2500000] (imputed) 6 response to statin, low density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0004611 GCST002675 Genome-wide genotyping array 2014-02-04 21946351 Stacey SN 2011-09-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21946351 A germline variant in the TP53 polyadenylation signal confers cancer susceptibility. Basal cell carcinoma 2,121 European ancestry cases, 39,614 European ancestry controls 2,506 European and other ancestry cases, 15,101 European and other ancestry controls Illumina [~ 16000000] (imputed) 1 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST001250 Genome-wide genotyping array 2015-05-19 24280982 Ruderfer DM 2013-11-26 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24280982 Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia. Schizophrenia or bipolar disorder Up to 4,528 European ancestry schizophrenia cases, up to 4,841 schizophrenia cases, up to 7,362 European ancestry bipolar disorder cases, up to 3,048 bipolar disorder cases, up to 11,637 European ancestry controls, up to 7,786 controls NA Affymetrix, Illumina [~ 1100000] (imputed) 12 bipolar disorder, schizophrenia http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST002295 Genome-wide genotyping array 2012-10-23 22872573 Hu L 2012-08-07 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/22872573 Genome-wide association study of prognosis in advanced non-small cell lung cancer patients receiving platinum-based chemotherapy. Response to platinum-based chemotherapy in non-small-cell lung cancer 528 Han Chinese ancestry cases 340 Han Chinese ancestry cases, 409 European ancestry cases NR [576351] 5 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST001629 Genome-wide genotyping array 2012-11-19 22881374 Cummings AC 2012-09-01 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/22881374 Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene. Alzheimer's disease (late onset) 109 Amish cases, 689 Amish controls NA Affymetrix [614963] 13 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST001658 Genome-wide genotyping array 2012-11-16 22936669 Julia A 2012-08-30 Gut www.ncbi.nlm.nih.gov/pubmed/22936669 A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300. Crohn's disease 1,277 European ancestry cases, 1,488 European ancestry controls 1,365 European ancestry cases, 1,396 European ancestry controls Illumina [508934] 10 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST001652 Genome-wide genotyping array 2015-07-07 25367360 Li Q 2014-11-04 Hum Genet www.ncbi.nlm.nih.gov/pubmed/25367360 Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium. Refractive astigmatism 8,487 European ancestry cases aged 25 years or older, 23,481 European ancestry controls aged 25 years or older, 907 European ancestry cases aged less than 25 years, 4,733 European ancestry controls aged less than 25 years, 3,076 Asian ancestry cases aged 25 years or older, 6,219 Asian ancestry controls aged 25 years or older, 247 Chinese ancestry cases aged less than 25 years, 670 Chinese ancestry controls aged less than 25 years NA Affymetrix, Illumina [NR] (imputed) 17 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST002685 Genome-wide genotyping array 2015-04-01 25030430 Zignego AL 2014-07-17 Genes Immun www.ncbi.nlm.nih.gov/pubmed/25030430 Genome-wide association study of hepatitis C virus- and cryoglobulin-related vasculitis. Mixed cryoglobulinemia vasculitis in chronic hepatitis C infection 356 European ancestry cases, 447 European ancestry controls 92 European ancestry cases, 179 European ancestry controls Illumina [899641] 2 cryoglobulinemia http://www.ebi.ac.uk/efo/EFO_0005846 GCST002534 Genome-wide genotyping array 2014-12-02 24755620 Perez-Palma E 2014-04-22 PLoS One www.ncbi.nlm.nih.gov/pubmed/24755620 Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies. Alzheimer's disease 2,540 European ancestry cases, 2,029 European ancestry controls NA Affymetrix, Illumina [1216213] (imputed) 5 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002422 Genome-wide genotyping array 2014-10-07 24444492 Kuo PH 2014-01-18 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24444492 Identification of novel loci for bipolar I disorder in a multi-stage genome-wide association study. Bipolar I disorder 200 Han Chinese ancestry cases, 200 Han Chinese ancestry controls 391 Han Chinese ancestry cases, 381 Han Chinese ancestry controls Illumina [249473] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST002338 Genome-wide genotyping array 2012-11-30 22961001 Su Z 2012-09-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/22961001 Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus. Barrett's esophagus Up to 1,852 European ancestry cases, 5,172 European ancestry controls 5,986 European ancestry cases, 12,825 European ancestry controls Illumina [521744] 5 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST001675 Genome-wide genotyping array 2015-05-15 23104005 Gudmundsson J 2012-10-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23104005 A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer. Prostate cancer 5,141 European ancestry cases, 54,444 European ancestry controls Up to 5,470 European ancestry cases, up to 7,583 European ancestry controls Illumina [~ 32500000] (imputed) 1 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001719 Genome-wide genotyping array 2012-11-13 22961961 Foroud T 2012-09-06 Stroke www.ncbi.nlm.nih.gov/pubmed/22961961 Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk. Intracranial aneurysm 1,483 European ancestry cases, 1,683 European ancestry controls NA Affymetrix [451088] 1 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST001665 Genome-wide genotyping array 2014-08-06 24778558 Domarkiene I 2013-12-01 Balkan J Med Genet www.ncbi.nlm.nih.gov/pubmed/24778558 RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families. Coronary heart disease 31 European ancestry cases and 63 European ancestry controls from 32 families NA Illumina [646445] 3 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST002298 Genome-wide genotyping array 2008-06-16 17982456 Plenge RM 2007-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/17982456 Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. Rheumatoid arthritis 397 European ancestry cases, 1,211 controls 1,408 cases, 2,426 controls, 875 European ancestry cases, 832 European ancestry controls Affymetrix [79853] 2 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST000122 Genome-wide genotyping array 2015-02-04 25043464 Jun G 2014-07-08 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/25043464 PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation. Alzheimer's disease 61 cases and 2,530 controls from 1,232 families 1,819 cases and 1,969 controls from 2,265 families, 9,966 European ancestry cases, 8,935 European ancestry controls, 1,459 African American cases, 3,437 African American controls, 951 Japanese ancestry cases, 894 Japanese ancestry controls Affymetrix [341492] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST002523 Genome-wide genotyping array 2009-01-16 19115949 Limou S 2009-01-01 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/19115949 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). AIDS progression 275 European ancestry seropositive non-progressors, 86 European ancestry seropositive rapid progressors, 1,352 European ancestry seronegative controls (see Fellay 2007) Illumina [291119] 3 AIDS http://www.ebi.ac.uk/efo/EFO_0000765 GCST000308 Genome-wide genotyping array 2015-05-07 25173106 Hysi PG 2014-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25173106 Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma. Intraocular pressure 7,738 Asian ancestry individuals, 27,558 European ancestry individuals NA Affymetrix, Illumina [~ 2500000] (imputed) 8 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST002580 Genome-wide genotyping array 2014-11-21 24800985 Agopian AJ 2014-05-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/24800985 Genome-wide association study of maternal and inherited loci for conotruncal heart defects. Conotruncal heart defects 537 European ancestry case-parent trios, 213 case-parent trios 348 European ancestry case-parent trios, 10 case-parent trios Illumina [2421290] (imputed) 11 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST002438 Genome-wide genotyping array 2015-01-14 24941225 Liang Y 2014-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/24941225 Genetic variations affecting serum carcinoembryonic antigen levels and status of regional lymph nodes in patients with sporadic colorectal cancer from Southern China. Elevated serum carcinoembryonic antigen levels 1,999 Chinese ancestry individuals NA Illumina [709211] (imputed) 13 serum carcinoembryonic antigen measurement http://www.ebi.ac.uk/efo/EFO_0005760 GCST002485 Genome-wide genotyping array 2014-11-19 24863034 Urano T 2014-05-23 Aging Cell www.ncbi.nlm.nih.gov/pubmed/24863034 Large-scale analysis reveals a functional single-nucleotide polymorphism in the 5'-flanking region of PRDM16 gene associated with lean body mass. Lean body mass 269 Japanese ancestry individuals 1,081 Japanese ancestry individuals Affymetrix [262000] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST002459 Genome-wide genotyping array 2011-08-22 21743467 Kote-Jarai Z 2011-07-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21743467 Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study. Prostate cancer 6,621 European ancestry cases, 6,939 European ancestry controls 22,957 European ancestry cases, 23,234 European ancestry controls, 420 East Asian ancestry cases, 433 East Asian ancestry controls, 112 African American cases, 298 African American controls, 7,140 cases, 5,455 controls NR [2600000] (imputed) 9 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST001148 Genome-wide genotyping array 2011-08-20 21804549 Torgerson DG 2011-07-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21804549 Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations. Asthma 2,088 European ancestry cases, 1,612 African American and African Caribbean cases, 1,688 Hispanic cases 2,727 European ancestry cases, 2,147 African American and African Caribbean cases, 2,299 Hispanic cases Affymetrix, Illumina [> 2000000] (imputed) 7 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST001182 Genome-wide genotyping array 2014-08-06 24429156 Noth I 2013-04-17 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/24429156 Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. Idiopathic pulmonary fibrosis 542 European ancestry cases, 542 European ancestry controls 868 European ancestry cases, 1,389 European ancestry controls Affymetrix [10601812] (imputed) 5 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST001974 Genome-wide genotyping array 2014-05-13 24192120 Kamide K 2013-11-01 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/24192120 Genome-wide response to antihypertensive medication using home blood pressure measurements: a pilot study nested within the HOMED-BP study. Blood pressure (response to antihypertensive medication) 265 Japanese ancestry individuals 79 Japanese ancestry individuals Affymetrix [298046] 0 blood pressure, response to antihypertensive drug http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0005405 GCST002262 Genome-wide genotyping array 2011-08-18 21771975 Chung CM 2011-07-19 Diabetes www.ncbi.nlm.nih.gov/pubmed/21771975 A genome-wide association study reveals a quantitative trait locus of adiponectin on CDH13 that predicts cardiometabolic outcomes. Adiponectin levels 382 Han Chinese ancestry young-onset-hypertensive cases 559 Han Chinese ancestry young-onset-hypertensive cases Illumina [509174] 1 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST001165 Genome-wide genotyping array 2014-10-23 24509480 Mahajan A 2014-02-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24509480 Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Type 2 diabetes 12,171 European ancestry cases, 56,862 European ancestry controls, 6,952 East Asian ancestry cases, 11,865 East Asian ancestry controls, 5,561 South Asian ancestry cases, 14,458 South Asian ancestry controls, 1,804 Mexican ancestry cases, 779 Mexican ancestry controls 21,491 European ancestry cases, 55,647 European ancestry controls Affymetrix, Illumina [2500000] (imputed) 62 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002352 Genome-wide genotyping array 2015-04-23 25133637 Scannell Bryan M 2014-08-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25133637 Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults. Body mass index 2,763 Bangladeshi ancestry females, 2,591 Bangladeshi ancestry males NA Illumina [1208102] (imputed) 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002571 Genome-wide genotyping array 2015-04-23 25133637 Scannell Bryan M 2014-08-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25133637 Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults. Body mass index (change over time) 2,643 Bangladeshi ancestry females, 2,340 Bangladeshi ancestry males NA Illumina [1208102] (imputed) 6 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST002575 Genome-wide genotyping array 2015-04-23 25133637 Scannell Bryan M 2014-08-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25133637 Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults. Height 2,754 Bangladeshi ancestry females, 2,590 Bangladeshi ancestry males NA Illumina [1208102] (imputed) 3 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST002573 Genome-wide genotyping array 2015-04-23 25133637 Scannell Bryan M 2014-08-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25133637 Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults. Underweight status 953 Bangladeshi ancestry underweight females, 1,269 Bangladeshi ancestry normal weight females, 1,146 Bangladeshi ancestry underweight males, 1,106 normal weight males NA Illumina [1208102] (imputed) 2 underweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005936 GCST002569 Genome-wide genotyping array 2015-06-02 25133637 Scannell Bryan M 2014-08-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/25133637 Genome-wide association studies and heritability estimates of body mass index related phenotypes in Bangladeshi adults. Overweight status 531 Bangladeshi ancestry overweight females, 1,269 Bangladeshi ancestry normal weight females, 338 Bangladeshi ancestry overweight males, 1,106 Bangladeshi ancestry normal weight males NA Illumina [1208102] (imputed) 3 overweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005935 GCST002570 Genome-wide genotyping array 2014-04-11 24513584 Oei L 2013-10-25 Bone www.ncbi.nlm.nih.gov/pubmed/24513584 Genome-wide Association Study for Radiographic Vertebral Fractures: A Potential Role for the 16q24 BMD Locus versus Lessons Learned from Challenging Phenotype Definition. Fractures (vertebral) 329 European ancestry cases, 2,666 European ancestry controls 5,619 European ancestry cases, 20,598 European ancestry controls, 101 Korean ancestry cases, 1,193 Korean ancestry controls Illumina [2543887] (imputed) 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST002244 Genome-wide genotyping array 2014-12-18 24942650 Terao C 2014-06-18 Arthritis Care Res (Hoboken) www.ncbi.nlm.nih.gov/pubmed/24942650 Effects of smoking and shared epitope on the production of anti-citrullinated peptide antibody in a Japanese adult population. Rheumatoid factor 3,170 Japanese ancestry individuals NA Illumina [394239] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST002489 Genome-wide genotyping array 2014-12-18 24942650 Terao C 2014-06-18 Arthritis Care Res (Hoboken) www.ncbi.nlm.nih.gov/pubmed/24942650 Effects of smoking and shared epitope on the production of anti-citrullinated peptide antibody in a Japanese adult population. Anti-citrullinated peptide antibody 3,170 Japanese ancestry individuals NA Illumina [394239] 0 anti-cyclic citrullinated peptide antibody measurement http://www.ebi.ac.uk/efo/EFO_0004733 GCST002488 Genome-wide genotyping array 2014-10-10 24518671 Nag A 2014-02-11 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24518671 A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort. Intraocular pressure 2,774 European ancestry individuals 22,789 European ancestry and Erasmus Rucphen individuals Illumina [~ 1870000] 1 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST002356 Genome-wide genotyping array 2014-05-12 24097068 Willer CJ 2013-10-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097068 Discovery and refinement of loci associated with lipid levels. LDL cholesterol 94,595 European ancestry individuals up to 4,420 African ancestry individuals NR [NR] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST002220 Genome-wide genotyping array 2014-05-13 24097068 Willer CJ 2013-10-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097068 Discovery and refinement of loci associated with lipid levels. Triglycerides 94,595 European ancestry individuals 8,743 East Asian ancestry individuals NR [NR] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST002219 Genome-wide genotyping array 2014-05-12 24097068 Willer CJ 2013-10-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097068 Discovery and refinement of loci associated with lipid levels. HDL cholesterol 94,595 European ancestry individuals 93,982 European ancestry individuals NR [NR] (imputed) 71 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST002223 Genome-wide genotyping array 2014-05-12 24097068 Willer CJ 2013-10-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097068 Discovery and refinement of loci associated with lipid levels. LDL cholesterol 94,595 European ancestry individuals 93,982 European ancestry individuals NR [NR] (imputed) 58 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST002222 Genome-wide genotyping array 2014-05-12 24097068 Willer CJ 2013-10-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097068 Discovery and refinement of loci associated with lipid levels. Cholesterol, total 94,595 European ancestry individuals 93,982 European ancestry individuals NR [NR] (imputed) 73 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST002221 Genome-wide genotyping array 2014-05-12 24097068 Willer CJ 2013-10-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097068 Discovery and refinement of loci associated with lipid levels. Triglycerides 94,595 European ancestry individuals 93,982 European ancestry individuals NR [NR] (imputed) 40 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST002216 Genome-wide genotyping array 2014-03-26 24065354 Al-Qahtani A 2013-09-24 J Med Genet www.ncbi.nlm.nih.gov/pubmed/24065354 Genome-wide association study of chronic hepatitis B virus infection reveals a novel candidate risk allele on 11q22.3. Liver disease in chronic hepatitis B virus infection up to 305 Arab ancestry cases, 343 Arab ancestry controls 48 Arab ancestry cases, 177 Arab ancestry controls Affymetrix [530480] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST002204 Genome-wide genotyping array 2014-11-01 24625756 Yu B 2014-03-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/24625756 Genetic determinants influencing human serum metabolome among African Americans. Serum metabolite levels 1,260 African American individuals NA Affymetrix [2341704] (imputed) 19 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST002388 Genome-wide genotyping array 2015-04-01 25035420 Hong KW 2014-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25035420 Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians. PR interval 6,085 Korean ancestry individuals 7,295 Japanese ancestry individuals Affymetrix [2100000] (imputed) 5 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST002535 Genome-wide genotyping array 2015-04-01 25035420 Hong KW 2014-07-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25035420 Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians. QRS duration 6,085 Korean ancestry individuals 7,295 Japanese ancestry individuals Affymetrix [2100000] (imputed) 6 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST002533 Genome-wide genotyping array 2015-02-05 24943344 Ferrari R 2014-07-01 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/24943344 Frontotemporal dementia and its subtypes: a genome-wide association study. Frontotemporal dementia 1,377 European ancestry behavioural variant cases, 308 European ancestry Semantic dementia cases, 269 European ancestry Progressive nonfluent aphasia cases, 200 European ancestry Frontotremporal dementia with motor neuron disease cases, up to 4,308 European ancestry controls 690 European ancestry behavioural variant cases, 190 European ancestry Semantic dementia cases, 221 European ancestry Progressive nonfluent aphasia cases, 94 European ancestry Frontotremporal dementia with motor neuron disease cases, 177 European ancestry Frontotemporal lobar degeneration cases, up to 5,094 European ancestry controls Illumina [6026385] (imputed) 2 frontotemporal dementia http://purl.obolibrary.org/obo/MONDO_0017276 GCST002516 Genome-wide genotyping array 2015-04-03 25085501 Bunyavanich S 2014-08-02 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/25085501 Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis. Allergic rhinitis in asthma 623 European ancestry cases, 1029 Latino cases, 399 African American/Afro-Caribbean cases, 488 European ancestry controls, 545 Latino controls, 162 African American/Afro-Caribbean controls NA Affymetrix, Illumina [NR] (imputed) 1 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST002552 Genome-wide genotyping array 2015-04-03 25085501 Bunyavanich S 2014-08-02 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/25085501 Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis. Allergic rhinitis in non-asthmatics 249 European ancestry cases, 164 Latino cases, 248 African American/Afro-Caribbean cases, 674 European ancestry controls, 588 Latino controls, 464 African American/Afro-Caribbean controls NA Affymetrix, Illumina [NR] (imputed) 7 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST002551 Genome-wide genotyping array 2015-04-01 25085501 Bunyavanich S 2014-08-02 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/25085501 Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis. Allergic rhinitis 872 European ancestry cases, 1,193 Latino cases, 647 African American/Afro-Caribbean cases, 1,162 European ancestry controls, 1,133 Latino controls, 626 African American/Afro-Caribbean controls NA Affymetrix, Illumina [NR] (imputed) 26 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST002550 Genome-wide genotyping array 2015-01-30 24886709 Ko A 2014-06-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24886709 Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. Cholesterol, total 3,701 Mexican ancestry individuals 5,114 Mexican ancestry individuals, 903 Mexican ancestry individuals from 73 dyslipidemic families Illumina [1661241] (imputed) 2 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST002467 Genome-wide genotyping array 2015-01-30 24886709 Ko A 2014-06-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24886709 Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. HDL cholesterol 3,701 Mexican ancestry individuals 5,114 Mexican ancestry individuals, 903 Mexican ancestry individuals from 73 dyslipidemic families Illumina [1661241] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST002469 Genome-wide genotyping array 2015-01-30 24886709 Ko A 2014-06-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24886709 Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. Triglycerides 1,678 Mexican ancestry high triglyceride cases, 1,645 Mexican ancestry low triglyceride controls 2,129 Mexican ancestry high triglyceride cases, 2,985 Mexican ancestry low triglyceride controls, 903 Mexican ancestry individuals from 73 dyslipidemic families Illumina [1661241] (imputed) 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST002468 Genome-wide genotyping array 2014-04-16 24098343 Polfus LM 2013-10-03 PLoS One www.ncbi.nlm.nih.gov/pubmed/24098343 Genome-wide association study of gene by smoking interactions in coronary artery calcification. Coronary artery calcification (smoking interaction) 915 European ancestry individuals 1,025 European ancestry individuals Affymetrix [2171047] (imputed) 0 smoking status measurement, coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004723 GCST002213 Genome-wide genotyping array 2015-06-11 25297839 Crosslin DR 2014-10-09 Genes Immun www.ncbi.nlm.nih.gov/pubmed/25297839 Genetic variation in the HLA region is associated with susceptibility to herpes zoster. Shingles 2,016 European ancestry cases, 16,407 European ancestry controls, 173 African ancestry cases, 3,312 African ancestry controls, 41 Hispanic cases, 580 Hispanic controls NA NR [NR] (imputed) 2 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST002654 Genome-wide genotyping array 2015-07-27 25500335 Tintle NL 2014-12-02 Prostaglandins Leukot Essent Fatty Acids www.ncbi.nlm.nih.gov/pubmed/25500335 A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study. Red blood cell fatty acid levels 2,633 individuals NA Affymetrix [~ 2500000] (imputed) 13 arachidonic acid measurement, fatty acid measurement, linolenic acid measurement, oleic acid measurement, docosapentaenoic acid measurement, linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006808, http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0006811, http://www.ebi.ac.uk/efo/EFO_0006810, http://www.ebi.ac.uk/efo/EFO_0006809, http://www.ebi.ac.uk/efo/EFO_0006807 GCST002712 Genome-wide genotyping array 2014-04-04 24097066 Li Y 2013-10-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24097066 A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. Sjögren's syndrome 542 Han Chinese ancestry cases, 1,050 Han Chinese ancestry controls 1,303 Han Chinese ancestry cases, 2,727 Han Chinese ancestry controls Affymetrix [556134] 5 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST002217 Genome-wide genotyping array 2010-07-13 20585324 Dick DM 2010-06-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20585324 Genome-wide association study of conduct disorder symptomatology. Conduct disorder (symptom count) 872 European, African American and other ancestry substance dependence cases, 3,091 European, African American and other ancestry controls NA Illumina [948658] 17 conduct disorder http://www.ebi.ac.uk/efo/EFO_0004216 GCST000713 Genome-wide genotyping array 2010-07-13 20585324 Dick DM 2010-06-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/20585324 Genome-wide association study of conduct disorder symptomatology. Conduct disorder 872 European, African American and other ancestry substance dependence cases, 3,091 European, African American and other ancestry controls NA Illumina [948658] 12 conduct disorder http://www.ebi.ac.uk/efo/EFO_0004216 GCST000714 Genome-wide genotyping array 2015-04-30 25173107 Chen Y 2014-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25173107 Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma. Glaucoma (high intraocular pressure) 966 Han Chinese ancestry cases, 1,005 Han Chinese ancestry controls 1,140 Han Chinese ancestry cases, 2,237 Han Chinese ancestry controls Illumina [870261] 2 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST002581 Genome-wide genotyping array 2014-05-01 24163127 Figueroa JD 2013-10-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24163127 Genome-wide association study identifies multiple loci associated with bladder cancer risk. Bladder cancer 6,911 European ancestry cases, 11,818 European ancestry controls 801 cases, 1,307 controls Illumina [462190] 7 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST002243 Genome-wide genotyping array 2014-05-01 24163127 Figueroa JD 2013-10-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24163127 Genome-wide association study identifies multiple loci associated with bladder cancer risk. Bladder cancer up to 2,305 European ancestry cases, up to 3,901 European ancestry controls up to 13,298 cases, up to 54,535 controls Illumina [462190] 10 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST002240 Genome-wide genotyping array 2015-06-18 25534755 Chaste P 2014-09-30 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25534755 A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity? Autism spectrum disorder-related traits 1633 European ancestry trios, 942 trios NA Illumina [up to 2017939] 6 autism spectrum disorder, autism, autism spectrum disorder symptom http://www.ebi.ac.uk/efo/EFO_0003756, http://www.ebi.ac.uk/efo/EFO_0003758, http://www.ebi.ac.uk/efo/EFO_0005426 GCST002639 Genome-wide genotyping array 2015-06-23 25189868 Sung YJ 2014-09-03 Am J Hypertens www.ncbi.nlm.nih.gov/pubmed/25189868 Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study. Blood pressure (smoking interaction) Up to 6,889 individuals NA Affymetrix [2485435] (imputed) 37 pack-years measurement, smoking behavior, smoking status measurement, diastolic blood pressure, systolic blood pressure, blood pressure, smoking behaviour measurement, cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006526, http://www.ebi.ac.uk/efo/EFO_0004318, http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0006525 GCST002587 Genome-wide genotyping array 2014-10-22 24513273 Yang B 2014-02-11 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/24513273 A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population. Serum uric acid levels 3,451 Han Chinese ancestry individuals 8,830 Chinese ancestry individuals Affymetrix, Illumina [658288] 4 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST002355 Genome-wide genotyping array 2014-11-06 24736177 Sprooten E 2014-04-13 Neuroimage www.ncbi.nlm.nih.gov/pubmed/24736177 Common genetic variants and gene expression associated with white matter microstructure in the human brain. White matter microstructure (global fractional anisotropy) 727 Mexican American individuals from 65 families, 49 Mexican American individuals NA Illumina [929187] 5 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST002409 Genome-wide genotyping array 2015-02-20 24939585 Fransen E 2014-06-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24939585 Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. Age-related hearing impairment 1,489 European ancestry individuals NA Illumina [4167292] (imputed) 30 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST002491 Genome-wide genotyping array 2015-02-20 24939585 Fransen E 2014-06-18 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24939585 Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment. Age-related hearing impairment (SNP x SNP interaction) 1,489 European ancestry individuals NA Illumina [629437] (imputed) 49 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST002487 Genome-wide genotyping array 2015-08-14 25533491 Rautanen A 2014-12-18 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/25533491 Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study. Sepsis from pneumonia (survival) 359 European ancestry non-survivor cases, 1,194 European ancestry survivor cases 106 European ancestry non-survivor cases, 432 European ancestry survivor cases Affymetrix, Illumina [5888277] (imputed) 2 survival time, pneumonia, septic shock, Sepsis http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0003106, http://www.ebi.ac.uk/efo/EFO_0006834, http://purl.obolibrary.org/obo/HP_0100806 GCST002725 Genome-wide genotyping array 2015-06-08 25352737 Ritchie MD 2014-09-19 Mol Vis www.ncbi.nlm.nih.gov/pubmed/25352737 Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci. Age-related cataracts 5,503 European, Black, and other ancestry cases age 50 and older, 1,894 European, Black, and other ancestry controls age 50 and older NA Illumina [530101] 3 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST002619 Genome-wide genotyping array 2015-06-08 25352737 Ritchie MD 2014-09-19 Mol Vis www.ncbi.nlm.nih.gov/pubmed/25352737 Electronic medical records and genomics (eMERGE) network exploration in cataract: several new potential susceptibility loci. Age-related cataracts (age at onset) 5,503 European, Black, and other ancestry cases age 50 and older NA Illumina [530101] 3 age of onset of cataract http://purl.obolibrary.org/obo/OBA_2001004 GCST002618 Genome-wide genotyping array 2015-04-16 25056061 Ripke S 2014-07-22 Nature www.ncbi.nlm.nih.gov/pubmed/25056061 Biological insights from 108 schizophrenia-associated genetic loci. Schizophrenia 32,405 European ancestry cases, 42,221 European ancestry controls, 1,235 European ancestry cases and 1,235 European ancestry controls from 1235 parent-offspring trios, 1,836 East Asian ancestry cases, 3,383 East Asian ancestry controls 1,513 European ancestry cases, 66,236 European ancestry controls Affymetrix, Illumina [9005918] (imputed) 98 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST002539 Genome-wide genotyping array 2014-10-29 24688116 Deelen J 2014-03-31 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24688116 Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age. Longevity (90 years and older) 5,406 European ancestry cases, 15,112 European ancestry controls 7,330 European ancestry cases, 61,156 European ancestry controls Illumina [2470825] (imputed) 3 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST002404 Genome-wide genotyping array 2014-10-29 24688116 Deelen J 2014-03-31 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24688116 Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age. Longevity (85 years and older) 7,729 European ancestry cases, 16,121 European ancestry controls 13,060 European ancestry cases, 61,156 European ancestry controls Illumina [2480356] (imputed) 4 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST002403 Genome-wide genotyping array 2015-06-08 25194280 Wei Q 2014-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25194280 Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population. Laryngeal squamous cell carcinoma 993 Chinese ancestry cases, 1,995 Chinese ancestry controls 2,398 Chinese ancestry cases, 2,804 Chinese ancestry controls Affymetrix [662108] 6 laryngeal squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0006352 GCST002597 Genome-wide genotyping array 2015-06-12 25310821 Kim JH 2014-10-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/25310821 A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. Hirschsprung disease 123 Korean ancestry cases, 432 Korean ancestry controls NA Illumina [757260] 6 Hirschsprung disease http://purl.obolibrary.org/obo/MONDO_0018309 GCST002658 Genome-wide genotyping array 2015-09-22 25526632 Rafiq S 2014-12-19 PLoS One www.ncbi.nlm.nih.gov/pubmed/25526632 A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis. Breast cancer (survival) 1,341 European ancestry cases 1,523 European ancestry cases Illumina [6500000] (imputed) 3 survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST002727 Genome-wide genotyping array 2018-09-12 23093944 Krumsiek J 2012-10-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23093944 Mining the unknown: a systems approach to metabolite identification combining genetic and metabolic information. Serum metabolite levels 1,678 European ancestry individuals NA Affymetrix [655658] 110 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST006249 Genome-wide genotyping array 2015-04-23 25060954 Wolber LE 2014-07-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25060954 Salt-inducible kinase 3, SIK3, is a new gene associated with hearing. Hearing function 1,022 European ancestry individuals, 280 Carlantino (founder/genetic isolate) individuals, 1,097 Friuli Venezia Giulia (founder/genetic isolate) individuals, 804 Korcula (founder/genetic isolate) individuals, 497 Split (founder/genetic isolate) individuals, 421 Cilento (founder/genetic isolate) individuals, 470 Talana (founder/genetic isolate) individuals, 348 Silk Road individuals NA Affymetrix, Illumina [> 2300000] (imputed) 5 sensory perception of sound http://purl.obolibrary.org/obo/GO_0007605 GCST002543 Genome-wide genotyping array 2015-05-11 25057126 Ramos YF 2014-07-23 J Med Genet www.ncbi.nlm.nih.gov/pubmed/25057126 Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance. Osteoarthritis biomarkers up to 4,654 European ancestry individuals 964 European ancestry individuals Illumina [up to 1961964] (imputed) 5 osteoarthritis biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005890 GCST002540 Genome-wide genotyping array 2014-03-14 23969696 Sabater-Lleal M 2013-08-22 Circulation www.ncbi.nlm.nih.gov/pubmed/23969696 Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Fibrinogen 91,323 European ancestry individuals 8,423 African American individuals, 1,447 Hispanic individuals Affymetrix, Illumina [2515567] (imputed) 24 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST002147 Genome-wide genotyping array 2014-07-10 21253498 Benjamin AM 2010-12-26 J Obes www.ncbi.nlm.nih.gov/pubmed/21253498 Gene by sex interaction for measures of obesity in the framingham heart study. Body mass index (sex interaction) 9,091 European ancestry individuals 2,872 European ancestry individuals Affymetrix [360811] 0 sex interaction measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004340 GCST000930 Genome-wide genotyping array 2014-07-10 21253498 Benjamin AM 2010-12-26 J Obes www.ncbi.nlm.nih.gov/pubmed/21253498 Gene by sex interaction for measures of obesity in the framingham heart study. Waist circumference (sex interaction) 2,314 European ancestry individuals 2,872 European ancestry individuals Affymetrix [360811] 0 waist circumference, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0008343 GCST000931 Genome-wide genotyping array 2014-07-10 21253498 Benjamin AM 2010-12-26 J Obes www.ncbi.nlm.nih.gov/pubmed/21253498 Gene by sex interaction for measures of obesity in the framingham heart study. Body mass index 9,091 European ancestry individuals 2,872 European ancestry individuals Affymetrix [360811] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST000929 Genome-wide genotyping array 2014-07-10 21253498 Benjamin AM 2010-12-26 J Obes www.ncbi.nlm.nih.gov/pubmed/21253498 Gene by sex interaction for measures of obesity in the framingham heart study. Waist-to-hip ratio (sex interaction) 2,314 European ancestry individuals NA Affymetrix [360811] 0 sex interaction measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004343 GCST000928 Genome-wide genotyping array 2015-06-18 25335168 Hashimoto R 2014-10-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/25335168 Common variants at 1p36 are associated with superior frontal gyrus volume. Superior frontal gyrus grey matter volume 158 Japanese ancestry schizophrenia cases, 378 Japanese ancestry healthy controls NA Affymetrix [517946] 11 superior frontal gyrus grey matter volume measurement http://www.ebi.ac.uk/efo/EFO_0006516 GCST002663 Genome-wide genotyping array 2014-07-01 21102462 Elks CE 2010-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/21102462 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Menarche (age at onset) 86,142 European ancestry female individuals, 557 Old Order Amish (founder/genetic isolate) female individuals, 1,103 Erasmus Rucphen (founder/genetic isolate) female individuals Up to 12,813 European ancestry female individuals, 910 Val Borbera (founder/genetic isolate) female individuals, 348 Orcadian (founder/genetic isolate) female individuals, 338 Friuli Venezia Giulia (founder/genetic isolate) female individuals, 322 Carlantino (founder/genetic/isolate) female individuals Affymetrix, Illumina [~ 2500000] (imputed) 42 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST000880 Genome-wide genotyping array 2015-07-24 25436638 Malinowski JR 2014-12-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/25436638 Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE Network. Serum thyroid-stimulating hormone levels 4,501 European ancestry individuals, 351 African American individuals NA Illumina [up to 905285] 18 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST002707 Genome-wide genotyping array 2015-07-07 25385369 Ramanan VK 2014-11-11 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/25385369 FASTKD2 is associated with memory and hippocampal structure in older adults. Episodic memory 5,283 European ancestry individuals, 817 African American individuals, 605 individuals 6,687 European ancestry individuals, 711 African American individuals, 363 individuals Illumina [1681327] 1 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST002695 Genome-wide genotyping array 2014-11-13 24763700 Vinayagamoorthy N 2014-04-24 PLoS One www.ncbi.nlm.nih.gov/pubmed/24763700 New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis. C-reactive protein levels 7,626 Korean ancestry individuals 903 Korean ancestry individuals Affymetrix [1219546] (imputed) 5 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST002424 Genome-wide genotyping array 2014-10-10 24687471 Harlaar N 2014-02-01 J Speech Lang Hear Res www.ncbi.nlm.nih.gov/pubmed/24687471 Genome-wide association study of receptive language ability of 12-year-olds. Receptive language ability 2,329 European ancestry individuals 2,639 European ancestry individuals Affymetrix [1700000] (imputed) 0 receptive language perception http://www.ebi.ac.uk/efo/EFO_0005686 GCST002344 Genome-wide genotyping array 2015-09-22 25461247 Lehmann DS 2015-02-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/25461247 Genome-wide association study of virologic response with efavirenz-containing or abacavir-containing regimens in AIDS clinical trials group protocols. Response to efavirenz-containing treatment in HIV 1 infection (virologic failure) Up to 737 European ancestry individuals, Up to 545 Black individuals, Up to 314 Hispanic individuals NA Illumina [> 8000000] (imputed) 35 response to efavirenz, virologic response measurement http://www.ebi.ac.uk/efo/EFO_0006904, http://www.ebi.ac.uk/efo/EFO_0006906 GCST002771 Genome-wide genotyping array 2015-09-21 25461247 Lehmann DS 2015-02-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/25461247 Genome-wide association study of virologic response with efavirenz-containing or abacavir-containing regimens in AIDS clinical trials group protocols. Response to abacavir-containing treatment in HIV-1 infection (virologic failure) Up 346 European ancestry individuals, Up to 265 Black individuals, Up to 175 Hispanic individuals NA Illumina [> 8000000] (imputed) 27 virologic response measurement, response to abacavir http://www.ebi.ac.uk/efo/EFO_0006906, http://www.ebi.ac.uk/efo/EFO_0006905 GCST002769 Genome-wide genotyping array 2015-06-12 25342443 Lindstrom S 2014-10-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25342443 Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Mammographic density (dense area) 7,600 European ancestry individuals 343 European ancestry individuals, 1,472 Old Order Amish individuals, 8,564 individuals Affymetrix, Illumina [~ 2500000] (imputed) 12 dense area measurement, mammographic density measurement http://www.ebi.ac.uk/efo/EFO_0006503, http://www.ebi.ac.uk/efo/EFO_0005941 GCST002667 Genome-wide genotyping array 2015-06-12 25342443 Lindstrom S 2014-10-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25342443 Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Mammographic density (non-dense area) 7,600 European ancestry individuals 343 European ancestry individuals, 1,472 Old Order Amish individuals, 8,564 individuals Affymetrix, Illumina [~ 2500000] (imputed) 8 non-dense area measurement, mammographic density measurement http://www.ebi.ac.uk/efo/EFO_0006504, http://www.ebi.ac.uk/efo/EFO_0005941 GCST002668 Genome-wide genotyping array 2015-06-13 25342443 Lindstrom S 2014-10-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25342443 Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk. Percent mammographic density 7,916 European ancestry individuals 343 European ancestry individuals, 1,472 Old Order Amish individuals, 8,564 individuals Affymetrix, Illumina [~ 2500000] (imputed) 5 mammographic density percentage, mammographic density measurement http://www.ebi.ac.uk/efo/EFO_0006502, http://www.ebi.ac.uk/efo/EFO_0005941 GCST002669 Genome-wide genotyping array 2015-04-16 25134534 Chen K 2014-08-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25134534 Genome-wide association study identifies new susceptibility loci for epithelial ovarian cancer in Han Chinese women. Epithelial ovarian cancer 1,044 Han Chinese ancestry cases, 1,172 Han Chinese ancestry controls 1,452 Han Chinese ancestry cases, 2,803 Han Chinese ancestry controls Illumina [710714] 6 malignant epithelial tumor of ovary http://purl.obolibrary.org/obo/MONDO_0018364 GCST002576 Genome-wide genotyping array 2014-02-21 23929743 Yadav S 2013-08-08 Stroke www.ncbi.nlm.nih.gov/pubmed/23929743 Genome-wide analysis of blood pressure variability and ischemic stroke. Blood pressure variability 3,802 European ancestry individuals 3,900 European ancestry individuals Illumina [~ 2500000] (imputed) 0 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST002116 Genome-wide genotyping array 2015-05-07 25108383 Geller F 2014-08-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25108383 Genome-wide association analyses identify variants in developmental genes associated with hypospadias. Hypospadias 1,006 European ancestry male child cases, 2,390 European ancestry male child controls, 3,096 European ancestry female child controls 1,972 European ancestry male child cases, 1,401 European ancestry male child controls, 405 European ancestry female child controls, 6 European ancestry child controls Illumina [8207076] (imputed) 24 hypospadias http://www.ebi.ac.uk/efo/EFO_0004209 GCST002563 Genome-wide genotyping array 2010-11-30 20953186 Huffmeier U 2010-10-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/20953186 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. Psoriatic arthritis 572 European ancestry cases, 888 European ancestry controls Up to 1,761 European ancestry cases, 3,727 European ancestry controls Affymetrix [1585307] (imputed) 3 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST000835 Genome-wide genotyping array 2014-11-06 24737549 Yoon KA 2014-04-15 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/24737549 Genetic variations associated with postoperative recurrence in stage I non-small cell lung cancer. Non-small cell lung cancer (recurrence rate) 250 Korean ancestry cases 308 Korean ancestry cases Affymetrix [308098] 2 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST002412 Genome-wide genotyping array 2010-09-17 20659327 Kariuki SN 2010-07-26 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/20659327 Trait-stratified genome-wide association study identifies novel and diverse genetic associations with serologic and cytokine phenotypes in systemic lupus erythematosus. Serologic markers in systemic lupus erythematosus 44 European, African American, Hispanic American, and Asian American high IFN-alpha cases, 60 European, African American, Hispanic American, and Asian American low IFN-alpha cases 280 African American cases, 173 European ancestry cases, 85 Hispanic American cases Affymetrix [NR] 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST000739 Genome-wide genotyping array 2014-11-06 24714607 Dijkstra AE 2014-04-08 PLoS One www.ncbi.nlm.nih.gov/pubmed/24714607 Susceptibility to chronic mucus hypersecretion, a genome wide association study. Chronic mucus hypersecretion 717 European ancestry cases, 2,385 European ancestry controls 1,963 European ancestry cases, 5,801 European ancestry controls, 24 Erasmus Rucphen cases, 28 Erasmus Rucphen controls Illumina [492700] 1 chronic mucus hypersecretion http://www.ebi.ac.uk/efo/EFO_0005673 GCST002407 Genome-wide genotyping array 2013-02-19 23241943 Clark SL 2012-12-12 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/23241943 Genome-wide association study of patient-rated and clinician-rated global impression of severity during antipsychotic treatment. Response to antipsychotic treatment Up to 421 European ancestry Schizophrenia cases, up to 214 African American individuals, up to 103 individuals NA Affymetrix [492900] 8 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST001773 Genome-wide genotyping array 2014-11-14 24827717 Yang F 2014-05-01 Biomed Environ Sci www.ncbi.nlm.nih.gov/pubmed/24827717 Genome wide association study: searching for genes underlying body mass index in the Chinese. Body mass index 597 Han Chinese ancestry individuals 2,955 Han Chinese ancestry individuals Affymetrix [281533] 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002435 Genome-wide genotyping array 2014-11-29 24836286 Zhang B 2014-05-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24836286 Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk. Colorectal cancer 2,098 East Asian ancestry cases, 6,172 East Asian ancestry controls 12,865 East Asian ancestry cases, 25,773 East Asian ancestry controls, up to 16,984 European ancestry cases, up to 18,262 European ancestry controls Affymetrix, Illumina [2400000] (imputed) 20 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002454 Genome-wide genotyping array 2014-10-15 24535457 Chouraki V 2014-02-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24535457 A genome-wide association meta-analysis of plasma Aβ peptides concentrations in the elderly. Plasma amyloid beta peptide concentrations (ABx-40) 3,528 European ancestry individuals NA Illumina [2316178] (imputed) 10 plasma beta-amyloid 1-40 measurement http://www.ebi.ac.uk/efo/EFO_0005659 GCST002360 Genome-wide genotyping array 2014-10-15 24535457 Chouraki V 2014-02-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/24535457 A genome-wide association meta-analysis of plasma Aβ peptides concentrations in the elderly. Plasma amyloid beta peptide concentrations (ABx-42) 3,528 European ancestry individuals NA Illumina [2316178] (imputed) 8 plasma beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0005660 GCST002359 Genome-wide genotyping array 2010-06-14 20485516 Lu Y 2010-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/20485516 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. Central corneal thickness 3,473 European ancestry twins in 1,905 families, 301 European ancestry thin CCT cases, 301 European ancestry thick CCT controls NA Illumina [~ 2400000] 2 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST000683 Genome-wide genotyping array 2010-03-09 20164292 Koller DL 2010-02-17 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/20164292 Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women. Bone mineral density 1,524 European ancestry female individuals from 762 sibships 669 African American female individuals from 383 sibships Illumina [547971] 0 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST000598 Genome-wide genotyping array 2015-07-08 25241763 Springelkamp H 2014-09-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25241763 Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process. Vertical cup-disc ratio 18,963 European ancestry individuals, 2,131 Erasmus Rucphen individuals 2,453 Chinese ancestry individuals, 2,026 Indian ancestry individuals, 2,305 Malay ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 18 optic disc size measurement http://www.ebi.ac.uk/efo/EFO_0004832 GCST002626 Genome-wide genotyping array 2015-09-19 25420145 Debette S 2014-11-24 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25420145 Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection. Cervical artery dissection 1,393 European ancestry cases, 14,416 European ancestry controls 659 European ancestry cases, 2,648 European ancestry controls Illumina [472862] 5 cervical artery dissection http://www.ebi.ac.uk/efo/EFO_1000059 GCST002700 Genome-wide genotyping array 2015-09-19 25514360 Hansel NN 2014-12-16 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/25514360 Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease. Airway responsiveness in chronic obstructive pulmonary disease Up to 4,108 European American cases NA Illumina [546355] 26 airway responsiveness measurement http://www.ebi.ac.uk/efo/EFO_0006897 GCST002724 Genome-wide genotyping array 2013-12-05 23753411 Turner ST 2013-06-10 Hypertension www.ncbi.nlm.nih.gov/pubmed/23753411 Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide. Response to diuretic therapy in hypertension 424 European ancestry individuals 841 European ancestry individuals Illumina [1092841] (imputed) 1 response to diuretic http://purl.obolibrary.org/obo/GO_0036270 GCST002067 Genome-wide genotyping array 2008-06-16 17293876 Sladek R 2007-02-11 Nature www.ncbi.nlm.nih.gov/pubmed/17293876 A genome-wide association study identifies novel risk loci for type 2 diabetes. Type 2 diabetes 661 European ancestry cases, 614 European ancestry controls 2,617 European ancestry cases, 2,894 European ancestry controls Illumina [392935] 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST000012 Genome-wide genotyping array 2014-11-13 24722205 Kwak SH 2014-04-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24722205 A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans. Free thyroxine concentration 2,789 Korean ancestry individuals 829 Korean ancestry individuals Affymetrix [1418709] (imputed) 3 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST002418 Genome-wide genotyping array 2014-11-13 24722205 Kwak SH 2014-04-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24722205 A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans. Thyroid peroxidase antibody positivity 377 Korean ancestry cases, 3,019 Korean ancestry anti-TPO controls 108 Korean ancestry cases, 734 Korean ancestry controls Affymetrix [1418709] (imputed) 2 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST002416 Genome-wide genotyping array 2014-11-13 24722205 Kwak SH 2014-04-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24722205 A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans. Plasma thyroid-stimulating hormone levels 2,789 Korean ancestry individuals 829 Korean ancestry individuals Affymetrix [1418709] (imputed) 3 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST002417 Genome-wide genotyping array 2014-11-01 24684796 Cox AJ 2014-03-11 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/24684796 Heritability and genetic association analysis of cognition in the Diabetes Heart Study. Cognitive function 423 type 2 diabetes cases and 127 unaffected siblings from 257 families NA Affymetrix [> 371951] (imputed) 25 cognition http://www.ebi.ac.uk/efo/EFO_0003925 GCST002386 Genome-wide genotyping array 2015-07-07 25383971 Dunstan SJ 2014-11-10 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25383971 Variation at HLA-DRB1 is associated with resistance to enteric fever. Enteric fever 432 Vietnamese ancestry cases, 2,011 Vietnamese ancestry controls 151 Vietnamese ancestry cases, 668 Vietnamese ancestry controls, 595 Nepalese ancestry cases, 386 Nepalese ancestry controls Illumina [709725] 1 typhoid fever http://www.ebi.ac.uk/efo/EFO_0006789 GCST002693 Genome-wide genotyping array 2015-04-01 25027321 Hoffmann TJ 2014-07-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25027321 Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative. Glaucoma 658 African American prevalent cases, 1,062 African American incident cases, 6,067 African American controls, 153 Hispanic prevalent cases, 336 Hispanic incident cases, 2,685 Hispanic controls NA Affymetrix [up to 15784307] (imputed) 8 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST002529 Genome-wide genotyping array 2015-04-28 24241537 Bonnelykke K 2013-11-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24241537 A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations. Asthma (childhood onset) 1,173 European ancestry cases, 2,511 European ancestry controls 395 European ancestry cases, 2,663 European ancestry controls, 63 Turkish, Surinamese, Dutch Antillean, Moroccan, Cape Verdian and other ancestry cases, 917 Turkish, Surinamese, Dutch Antillean, Moroccan, Cape Verdian and other ancestry controls, 6,783 cases, 7,720 controls Affymetrix, Illumina [124514] 6 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST002275 Genome-wide genotyping array 2015-04-23 25080503 Kwan JS 2014-07-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/25080503 Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels. Osteoprotegerin levels 4,158 European ancestry males, 531 South Tyrol males, 4,253 European ancestry females, 692 South Tyrol females, 702 Han Chinese ancestry females NA Affymetrix, Illumina [up to 2544063] (imputed) 4 osteoprotegerin measurement http://www.ebi.ac.uk/efo/EFO_0005918 GCST002546 Genome-wide genotyping array 2014-10-10 24383474 Manichaikul A 2014-01-02 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/24383474 Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study. Pulmonary emphysema 2,587 European ancestry individuals, 2,510 African American individuals, 2,113 Hispanic individuals, 704 Chinese ancestry individuals 6,023 European ancestry individuals Affymetrix [897981] 3 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST002326 Genome-wide genotyping array 2014-06-24 21124955 Marzi C 2010-11-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/21124955 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. Amyloid A serum levels 3,329 European ancestry individuals, 882 Sorbian (founder/genetic isolate) individuals 2,136 European ancestry individuals Affymetrix, Illumina [2593456] (imputed) 4 serum amyloid A protein measurement http://www.ebi.ac.uk/efo/EFO_0004728 GCST000876 Genome-wide genotyping array 2015-08-20 25329471 van Leeuwen EM 2014-10-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/25329471 The challenges of genome-wide interaction studies: lessons to learn from the analysis of HDL blood levels. HDL cholesterol (SNP x SNP interaction) 2,996 European ancestry indivdiuals 2,755 Erasmus Rucphen individuals, 12,276 European ancestry individuals, 18,203 individuals Illumina [495508] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST002661 Genome-wide genotyping array 2014-11-07 24753544 Knipe DW 2014-04-21 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/24753544 Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies. Prostate cancer 1,146 European ancestry cases, 1,804 European ancestry controls 1,854 European ancestry cases, 1,437 European ancestry controls Illumina [514432] (imputed) 6 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST002421 Genome-wide genotyping array 2013-09-24 19901119 Trevino LR 2009-11-09 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/19901119 Germline genetic variation in an organic anion transporter polypeptide associated with methotrexate pharmacokinetics and clinical effects. Methotrexate pharmacokinetics (acute lymphoblastic leukemia) 315 European ancestry cases, 73 African American cases, 5 Asian ancestry cases, 247 cases NA Affymetrix [398699] 21 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST000523 Genome-wide genotyping array 2015-07-07 25383866 Kirkpatrick RM 2014-11-10 PLoS One www.ncbi.nlm.nih.gov/pubmed/25383866 Results of a "GWAS plus:" general cognitive ability is substantially heritable and massively polygenic. General cognitive ability 7,100 European ancestry individuals NA Illumina [2546647] (imputed) 3 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST002694 Genome-wide genotyping array 2009-12-04 19910028 Mathias RA 2009-11-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/19910028 A genome-wide association study on African-ancestry populations for asthma. Asthma 464 African American cases, 471 African American controls, 355 African Caribbean ancestry cases and 574 African Caribbean ancestry controls from 163 families 994 European ancestry cases, 1,243 European ancestry controls, 2,331 African American cases, 2,874 African American controls Illumina [~ 644503] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST000525 Genome-wide genotyping array 2009-09-28 18195134 Byun E 2008-01-14 Arch Neurol www.ncbi.nlm.nih.gov/pubmed/18195134 Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis. Response to interferon beta therapy 99 European ancestry responders, 107 European ancestry non-responders 81 European ancestry individuals Affymetrix [~ 100000] 0 response to interferon-beta http://purl.obolibrary.org/obo/GO_0035456 GCST000140 Genome-wide genotyping array 2019-03-20 25200001 Robinson PC 2014-09-08 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/25200001 Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis. Acute anterior uveitis (with or without ankylosing spondylitis) 238 European ancestry primary acute anterior uveitis cases, 1,199 European ancestry cases with acute anterior uveitis and ankylosing spondylitis, 9,564 European ancestry controls NR Illumina [at least 106525] (imputed) 14 anterior uveitis http://www.ebi.ac.uk/efo/EFO_1000811 GCST007362 Targeted genotyping array [ImmunoChip] 2019-03-20 25200001 Robinson PC 2014-09-08 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/25200001 Genetic dissection of acute anterior uveitis reveals similarities and differences in associations observed with ankylosing spondylitis. Acute anterior uveitis in ankylosing spondylitis 1,199 European ancestry cases, 1,731 European ancestry controls NR Illumina [at least 106525] (imputed) 4 anterior uveitis http://www.ebi.ac.uk/efo/EFO_1000811 GCST007361 Targeted genotyping array [ImmunoChip] 2014-03-22 24029427 Sandholm N 2013-09-12 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/24029427 Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes. End-stage renal disease in Type 1 diabetics 258 European ancestry female cases, 935 European ancestry female controls, 387 European ancestry male cases, 655 European ancestry male controls 178 European ancestry female cases, 594 European ancestry female controls, 251 European ancestry male cases, 494 European ancestry male controls, 252 female cases, 479 female controls, 256 male cases, 342 male controls Illumina [2400000] (imputed) 1 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST002182 Genome-wide genotyping array 2014-11-06 24770850 Cousminer DL 2014-04-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24770850 Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. Puberty onset (genital enlargement) 3,769 European ancestry boys 208 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 1 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST002426 Genome-wide genotyping array 2014-11-07 24770850 Cousminer DL 2014-04-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24770850 Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. Puberty onset (breast development) 6,147 European ancestry girls NA Affymetrix, Illumina [~ 2500000] (imputed) 2 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST002427 Genome-wide genotyping array 2014-11-07 24770850 Cousminer DL 2014-04-25 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24770850 Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty. Puberty onset 6,147 European ancestry girls, 3,769 European ancestry boys Up to 1,376 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST002425 Genome-wide genotyping array 2012-09-26 22837380 Fischer A 2012-07-26 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/22837380 A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1. Sarcoidosis 564 European ancestry cases, 1,575 European ancestry controls 3,080 European ancestry cases, 3,659 European ancestry controls Affymetrix [1294967] (imputed) 1 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST001622 Genome-wide genotyping array 2009-06-04 19451621 Landers JE 2009-05-18 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/19451621 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 1,821 cases, 2,258 controls 538 cases, 556 controls Illumina [288357] 16 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST000406 Genome-wide genotyping array 2014-02-08 23897914 Wang H 2013-07-29 Pediatrics www.ncbi.nlm.nih.gov/pubmed/23897914 A genome-wide association study (GWAS) for bronchopulmonary dysplasia. Bronchopulmonary dysplasia 117 African American newborn cases, 108 African American newborn controls, 448 Hispanic newborn cases, 460 Hispanic newborn controls, 74 Asian or Pacific Islander ancestry newborn cases, 93 Asian or Pacific Islander ancestry newborn controls, 174 European ancestry newborn cases, 216 European ancestry newborn controls, 14 newborn cases, 22 newborn controls 371 newborn cases, 424 newborn controls Illumina [1795103] 26 bronchopulmonary dysplasia http://purl.obolibrary.org/obo/MONDO_0019091 GCST002104 Genome-wide genotyping array 2012-11-02 22949513 EPICURE Consortium 2012-09-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22949513 Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32. Generalized epilepsy 702 European ancestry genetic absence epilepsies cases, 586 European ancestry juvenile myoclonic epilepsy cases, 239 European ancestry other genetic generalized epilepsies cases, 2,461 European ancestry controls 347 European ancestry genetic absence epilepsies trios, 166 European ancestry juvenile myoclonic epilepsy trios, 91 European ancestry other genetic generalized epilepsies trios, 385 European ancestry genetic absence epilepsies cases, 382 European ancestry juvenile myoclonic epilepsy cases, 122 European ancestry other genetic generalized epilepsies cases, up to 889 European ancestry controls Affymetrix [4560000] (imputed) 10 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST001662 Genome-wide genotyping array 2015-01-15 24954895 Simino J 2014-06-19 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24954895 Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. Blood pressure 55,796 European ancestry individuals 43,445 European ancestry individuals, 1,849 Chinese ancestry individuals, 2,502 Malay ancestry individuals, 2,476 Asian Indian ancestry individuals, 1,855 Asian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 28 blood pressure http://www.ebi.ac.uk/efo/EFO_0004325 GCST002497 Genome-wide genotyping array 2015-01-15 24954895 Simino J 2014-06-19 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24954895 Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia. Blood pressure (age interaction) 55,796 European ancestry individuals 43,445 European ancestry individuals, 1,849 Chinese ancestry individuals, 2,502 Malay ancestry individuals, 2,476 Asian Indian ancestry individuals, 1,855 Asian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 3 blood pressure, age at assessment http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0008007 GCST002495 Genome-wide genotyping array 2015-05-09 25064007 Nakajima M 2014-07-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/25064007 A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine. Ossification of the posterior longitudinal ligament of the spine 1,112 Japanese ancestry cases, 6,810 Japanese ancestry controls 548 Japanese ancestry cases, 6,469 Japanese ancestry controls Illumina [5163786] (imputed) 8 ossification of the posterior longitudinal ligament of the spine http://www.ebi.ac.uk/efo/EFO_0005895 GCST002545 Genome-wide genotyping array 2013-10-30 23670970 Blackman SM 2013-05-13 Diabetes www.ncbi.nlm.nih.gov/pubmed/23670970 Genetic modifiers of cystic fibrosis-related diabetes. Cystic fibrosis-related diabetes 644 cystic fibrosis-related diabetes cases, 2,415 cystic fibrosis controls 124 cystic fibrosis-related diabetes cases, 570 cystic fibrosis controls Illumina [549869] 1 cystic fibrosis, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0009061, http://purl.obolibrary.org/obo/MONDO_0005148 GCST002025 Genome-wide genotyping array 2012-10-28 22936694 Jin G 2012-08-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/22936694 Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men. Androgen levels 3,225 European ancestry male individuals NA Illumina [642461] 6 dihydrotestosterone measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004909, http://www.ebi.ac.uk/efo/EFO_0004908 GCST001653 Genome-wide genotyping array 2013-12-12 23776197 Leandro-Garcia LJ 2013-06-17 J Med Genet www.ncbi.nlm.nih.gov/pubmed/23776197 Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy. Paclitaxel-induced neuropathy 143 European ancestry individuals Illumina [518577] 10 methylcobalamin deficiency type cblE, brain serotonin transporter measurement http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0004569 GCST002074 Genome-wide genotyping array 2012-11-02 22939635 Reiner AP 2012-08-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/22939635 Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women. C-reactive protein 8,280 African American female individuals, 3,548 Hispanic female individuals 3,787 African American female individuals, 3,548 Hispanic female individuals, 5,656 European ancestry individuals Affymetrix [up to 2203609] (imputed) 11 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST001650 Genome-wide genotyping array 2013-03-20 23401653 Guggenheim JA 2013-01-03 Mol Vis www.ncbi.nlm.nih.gov/pubmed/23401653 A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans. Corneal curvature 2,023 European ancestry children 2,008 Chinese ancestry adult individuals, 2,281 Malay ancestry adult individuals, 2,142 Indian ancestry adult individuals, 929 Chinese ancestry children Illumina [2543887] (imputed) 1 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST001803 Genome-wide genotyping array 2014-12-05 24842889 Vacic V 2014-05-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24842889 Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes. Parkinson's disease 1,130 Ashkenazi Jewish cases, 2,611 Ashkenazi Jewish controls 306 Ashkenazi Jewish cases, 2,583 Ashkenazi Jewish controls Affymetrix, Illumina [1069161] (imputed) 4 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST002455 Genome-wide genotyping array 2013-11-15 23719583 Kerns SL 2013-05-26 Radiother Oncol www.ncbi.nlm.nih.gov/pubmed/23719583 Genome-wide association study identifies a region on chromosome 11q14.3 associated with late rectal bleeding following radiation therapy for prostate cancer. Adverse response to radiation therapy 79 European, African, Asian, and Hispanic ancestry cases, 241 European, African, Asian, and Hispanic ancestry controls 107 European, African, Asian, and Hispanic ancestry cases, 671 European, African, Asian, and Hispanic ancestry controls Affymetrix [614453] 3 response to radiation http://purl.obolibrary.org/obo/GO_0009314 GCST002034 Genome-wide genotyping array 2014-07-22 24253340 Lencz T 2013-11-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/24253340 Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder. Schizophrenia 904 Ashkenazi Jewish cases, 1,640 Ashkenazi Jewish controls 3,944 European ancestry cases, 3,049 European ancestry controls, 921 African American cases, 954 African American controls, 550 Japanese ancestry cases, 530 Japanese ancestry controls Illumina [762372] 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST002277 Genome-wide genotyping array 2015-04-01 25028398 Weiss FU 2014-07-15 Gut www.ncbi.nlm.nih.gov/pubmed/25028398 Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study. Serum lipase activity 3,966 European ancestry individuals 1,444 European ancestry individuals Affymetrix [NR] (imputed) 2 serum lipase activity measurement http://www.ebi.ac.uk/efo/EFO_0005849 GCST002530 Genome-wide genotyping array 2015-04-01 25028398 Weiss FU 2014-07-15 Gut www.ncbi.nlm.nih.gov/pubmed/25028398 Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study. High serum lipase activity 981 European ancestry cases, 2985 European ancestry controls 346 European ancestry cases, 1098 European ancestry controls Affymetrix [NR] (imputed) 1 serum lipase activity measurement http://www.ebi.ac.uk/efo/EFO_0005849 GCST002532 Genome-wide genotyping array 2008-06-27 18449908 Poduslo SE 2008-04-30 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/18449908 Genome screen of late-onset Alzheimer's extended pedigrees identifies TRPC4AP by haplotype analysis. Alzheimer's disease 11 European ancestry cases and 19 European ancestry controls from 2 affected families, 60 controls 199 European ancestry cases, 85 European ancestry controls Affymetrix [469218] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST000183 Genome-wide genotyping array 2013-12-12 23823136 Larsen MH 2013-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/23823136 Genome-Wide Association Study of Genetic Variants in LPS-Stimulated IL-6, IL-8, IL-10, IL-1ra and TNF-α Cytokine Response in a Danish Cohort. Lipopolysaccharide induced cytokine levels 130 European ancestry individuals 586 European ancestry individuals Affymetrix [500000] 0 cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004873 GCST002075 Genome-wide genotyping array 2013-03-05 23218918 Sprooten E 2012-12-04 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/23218918 White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder. White matter integrity 70 unaffected relatives of cases with bipolar disorder, 80 controls NA Illumina [565404] 7 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST001760 Genome-wide genotyping array 2013-03-05 23218918 Sprooten E 2012-12-04 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/23218918 White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder. White matter integrity (bipolar disorder risk interaction) 70 unaffected relatives of cases with bipolar disorder, 80 controls NA Illumina [565404] 6 bipolar disorder, white matter integrity http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0004641 GCST001764 Genome-wide genotyping array 2014-03-07 23967269 Kim JH 2013-08-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/23967269 A genome-wide association study of total serum and mite-specific IgEs in asthma patients. IgE levels in asthmatics 877 Korean ancestry cases NA Illumina [442089] 4 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST002122 Genome-wide genotyping array 2014-03-07 23967269 Kim JH 2013-08-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/23967269 A genome-wide association study of total serum and mite-specific IgEs in asthma patients. IgE levels in asthmatics (D.p. specific) 329 Korean ancestry D.p.-positive cases, 548 Korean ancestry D.p.-negative cases NA Illumina [442089] 3 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST002124 Genome-wide genotyping array 2014-03-07 23967269 Kim JH 2013-08-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/23967269 A genome-wide association study of total serum and mite-specific IgEs in asthma patients. IgE levels in asthmatics (D.f. specific) 404 Korean ancestry D.f.-positive cases, 473 Korean ancestry D.f.-negative cases NA Illumina [442089] 2 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST002125 Genome-wide genotyping array 2015-06-06 24954085 Della-Morte D 2014-06-14 J Neurol Sci www.ncbi.nlm.nih.gov/pubmed/24954085 Novel genetic variants modify the effect of smoking on carotid plaque burden in Hispanics. Carotid plaque burden (smoking interaction) 665 Hispanic individuals 264 Hispanic indivduals Affymetrix [722379] 4 smoking behaviour measurement, carotid plaque build http://www.ebi.ac.uk/efo/EFO_0005671, http://www.ebi.ac.uk/efo/EFO_0006501 GCST002482 Genome-wide genotyping array 2014-10-09 24387768 Xu W 2014-01-04 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/24387768 Genome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1. Bipolar disorder 912 European ancestry cases, 903 European ancestry controls 636 individuals from 224 trios Illumina [502877] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST002327 Genome-wide genotyping array 2014-10-02 24392092 Luksys G 2014-01-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/24392092 BAIAP2 is related to emotional modulation of human memory strength. Memory performance 1,241 European ancestry individuals NA Affymetrix [587111] 1 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST002325 Genome-wide genotyping array 2015-05-26 25158072 Yu D 2014-10-31 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/25158072 Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD. Tourette's syndrome or obsessive-compulsive disorder 1,310 Ashkenazi Jewish, South African Afrikaner ancestry, and other European ancestry OCD cases, 834 Ashkenazi Jewish, French Canadian and other European ancestry Tourette's Syndrome cases, 579 Ashkenazi Jewish, South African Afrikaner ancestry, French Canadian and other European ancestry OCD and Tourette's syndrome cases, 4,975 European ancestry controls, 338 Ashkenazi Jewish controls, 196 French Canadian controls, 158 South African Afrikaner ancestry controls, 290 European ancestry OCD parent-child trios NA Illumina [7659573] (imputed) 15 obsessive-compulsive disorder, Tourette syndrome http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0004895 GCST002682 Genome-wide genotyping array 2012-11-13 22956598 Peters MJ 2012-09-06 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/22956598 Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region. Pain 1,308 European ancestry female cases, 5,791 European ancestry female controls 1,480 European ancestry female cases, 7,989 European ancestry female controls Illumina [2224068] (imputed) 1 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST001668 Genome-wide genotyping array 2015-04-01 25044758 Stergiakouli E 2014-07-21 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/25044758 Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3. Height adjusted BMI 5,809 children 2,089 European ancestry children Illumina [2608006] (imputed) 2 height-adjusted body mass index http://www.ebi.ac.uk/efo/EFO_0005851 GCST002538 Genome-wide genotyping array 2015-09-15 25387707 Vaidyanathan U 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387707 Heritability and molecular genetic basis of antisaccade eye tracking error rate: a genome-wide association study. Anti-saccade response 4,469 European ancestry twins and their parents NA Illumina [527829] 5 antisaccade response measurement http://www.ebi.ac.uk/efo/EFO_0006874 GCST002710 Genome-wide genotyping array 2011-07-08 21694764 Martin NW 2011-06-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/21694764 Educational attainment: a genome wide association study in 9538 Australians. Educational attainment 9,538 European ancestry individuals 968 European ancestry individuals Illumina [2493946] (imputed) 0 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST001097 Genome-wide genotyping array 2014-11-08 24737748 Whiffin N 2014-04-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24737748 Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis. Colorectal cancer 5,626 European ancestry cases, 7,817 European ancestry controls 14,037 European ancestry cases, 15,937 European ancestry controls Illumina [NR] (imputed) 9 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST002411 Genome-wide genotyping array 2014-12-13 24929828 Loth DW 2014-06-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24929828 Genome-wide association analysis identifies six new loci associated with forced vital capacity. Lung function (forced vital capacity) 52,253 European ancestry indiviudals 32,917 European ancestry individuals, 6,070 African American individuals, 849 Hispanic individuals, 8,637 East Asian ancestry individuals Affymetrix, Illumina [2762059] (imputed) 7 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST002483 Genome-wide genotyping array 2015-07-27 25483131 Ghassibe-Sabbagh M 2014-12-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/25483131 T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility. Type 2 diabetes 1,384 Lebanese ancestry cases, 1,902 Lebanese ancestry controls NA Illumina [5891794] (imputed) 6 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST002718 Genome-wide genotyping array 2010-04-08 20237162 Bozaoglu K 2010-03-17 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/20237162 Chemerin, a novel adipokine in the regulation of angiogenesis. Chemerin levels 858 Mexican American family members and individuals NA Illumina [542944] 7 chemerin measurement http://www.ebi.ac.uk/efo/EFO_0004573 GCST000628 Genome-wide genotyping array 2009-02-26 19117981 Sun J 2009-01-01 Cancer Res www.ncbi.nlm.nih.gov/pubmed/19117981 Sequence variants at 22q13 are associated with prostate cancer risk. Prostate cancer 1,235 European ancestry aggressive cases, 1,599 European ancestry controls 1,215 European ancestry aggressive cases, 2,213 European ancestry non-aggressive cases, 1,208 European ancestry controls, 1,034 aggressive cases, 921 non-aggressive cases, 2,231 controls Affymetrix, Illumina [~ 2000000] (imputed) 1 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST000307 Genome-wide genotyping array 2015-04-16 24952745 Arking DE 2014-06-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24952745 Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. QT interval Up to 70,389 European ancestry individuals, up to 672 Orcadian individuals Up to 33,316 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 74 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST002500 Genome-wide genotyping array 2014-11-02 24516586 Wu T 2014-02-06 PLoS One www.ncbi.nlm.nih.gov/pubmed/24516586 Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate. Cleft plate (environmental tobacco smoke interaction) 259 Asian ancestry cases and their unaffected parents, 272 European ancestry cases and their unaffected parents, 19 cases and their unaffected parents NA Illumina [~ 498000] 1 Cleft palate, environmental tobacco smoke exposure measurement http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0008361 GCST002348 Genome-wide genotyping array 2019-02-14 25442119 McLaughlin RL 2014-09-06 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/25442119 Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 605 European ancestry cases, 1,179 European ancestry controls NA Affymetrix, Illumina [2092686] (imputed) 0 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST007144 Genome-wide genotyping array 2019-02-14 25442119 McLaughlin RL 2014-09-06 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/25442119 Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 25 European ancestry C9orf72-positive cases, 1,179 European ancestry controls NA Affymetrix, Illumina [1172473] (imputed) 1 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST007146 Genome-wide genotyping array 2019-02-14 25442119 McLaughlin RL 2014-09-06 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/25442119 Second-generation Irish genome-wide association study for amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis (age of onset) 605 European ancestry cases, 1,179 European ancestry controls NA Affymetrix, Illumina [2093056] (imputed) 0 age of onset of amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/OBA_2001018 GCST007145 Genome-wide genotyping array 2014-02-06 23838604 Pare G 2013-07-08 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/23838604 Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema. Angioedema in response to angiotensin-converting enzyme inhibitor 175 European, African American and other ancestry ACE inhibitor-associated angioedema cases, 489 European, African American and other ancestry ACE inhibitor-exposed controls 19 European, African American and other ancestry ACE inhibitor-associated angioedema cases, 57 European, African American and other ancestry ACE inhibitor-exposed controls Illumina [579344] 0 response to angiotensin-converting enzyme inhibitor, angioedema http://www.ebi.ac.uk/efo/EFO_0005325, http://www.ebi.ac.uk/efo/EFO_0005532 GCST002091 Genome-wide genotyping array 2015-06-18 25223841 Li J 2014-09-13 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/25223841 A genetic locus in 7p12.2 associated with treatment resistant schizophrenia. Schizophrenia (treatment resistant) 79 European ancestry treatment resistant cases, 95 European ancestry non-treatment resistant cases 70 European ancestry treatment resistant cases, 125 European ancestry non-treatment resistant cases Illumina [552419] 1 treatment refractory schizophrenia http://www.ebi.ac.uk/efo/EFO_0004609 GCST002604 Genome-wide genotyping array 2013-11-29 23728906 Byrne EM 2013-05-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23728906 A genome-wide association study of sleep habits and insomnia. Sleep time 2,322 European ancestry individuals NA Illumina [2380486] (imputed) 5 sleep time http://www.ebi.ac.uk/efo/EFO_0005274 GCST002050 Genome-wide genotyping array 2013-11-29 23728906 Byrne EM 2013-05-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23728906 A genome-wide association study of sleep habits and insomnia. Sleep quality 2,315 European ancestry individuals NA Illumina [2380486] (imputed) 7 sleep quality http://www.ebi.ac.uk/efo/EFO_0005272 GCST002049 Genome-wide genotyping array 2013-11-29 23728906 Byrne EM 2013-05-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23728906 A genome-wide association study of sleep habits and insomnia. Sleep depth 2,314 European ancestry individuals NA Illumina [2380486] (imputed) 2 sleep depth http://www.ebi.ac.uk/efo/EFO_0005273 GCST002054 Genome-wide genotyping array 2013-11-29 23728906 Byrne EM 2013-05-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23728906 A genome-wide association study of sleep habits and insomnia. Sleep duration 2,278 European ancestry individuals NA Illumina [2380486] (imputed) 7 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST002053 Genome-wide genotyping array 2013-11-29 23728906 Byrne EM 2013-05-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23728906 A genome-wide association study of sleep habits and insomnia. Insomnia 2,267 European ancestry individuals NA Illumina [2380486] (imputed) 3 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST002052 Genome-wide genotyping array 2013-11-29 23728906 Byrne EM 2013-05-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/23728906 A genome-wide association study of sleep habits and insomnia. Sleep latency 2,280 European ancestry individuals 2,001 European ancestry individuals Illumina [2380486] (imputed) 0 sleep latency http://www.ebi.ac.uk/efo/EFO_0005280 GCST002051 Genome-wide genotyping array 2014-04-10 24057671 Chimusa ER 2013-09-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24057671 Genome-wide association study of ancestry-specific TB risk in the South African Coloured population. Tuberculosis 642 South African coloured cases, 91 South African coloured controls NA Affymetrix [up to 4467279] (imputed) 25 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST002198 Genome-wide genotyping array 2014-04-10 24057671 Chimusa ER 2013-09-18 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/24057671 Genome-wide association study of ancestry-specific TB risk in the South African Coloured population. Tuberculosis 642 South African coloured cases, 91 South African coloured controls, (see Thye 2010) NA Affymetrix [1009364] (imputed) 2 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST002197 Genome-wide genotyping array 2015-06-25 25293881 Patel YM 2014-10-07 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/25293881 The contribution of common genetic variation to nicotine and cotinine glucuronidation in multiple ethnic/racial populations. Cotinine glucuronidation 437 European ancestry current smoker individuals, 364 African American current smoker individuals, 453 Latino current smoker individuals, 674 Japanese ancestry current smoker individuals, 311 Native Hawaiian ancestry current smoker individuals NA Illumina [11892802] (imputed) 14 cotinine glucuronidation measurement http://www.ebi.ac.uk/efo/EFO_0006508 GCST002652 Genome-wide genotyping array 2015-06-26 25293881 Patel YM 2014-10-07 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/25293881 The contribution of common genetic variation to nicotine and cotinine glucuronidation in multiple ethnic/racial populations. Nicotine glucouronidation 437 European ancestry current smoker individuals, 364 African American current smoker individuals, 453 Latino current smoker individuals, 674 Japanese ancestry current smoker individuals, 311 Native Hawaiian ancestry current smoker individuals NA Illumina [11892802] (imputed) 2 nicotine glucuronidation measurement http://www.ebi.ac.uk/efo/EFO_0006507 GCST002649 Genome-wide genotyping array 2015-01-21 24980573 Song F 2014-06-30 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/24980573 Identification of a melanoma susceptibility locus and somatic mutation in TET2. Melanoma 494 European ancestry cases, 5,628 European ancestry controls 5,383 European ancestry cases, 13,033 European ancestry controls Affymetrix, Illumina [1579307] (imputed) 6 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST002514 Genome-wide genotyping array 2015-11-17 25631615 Springelkamp H 2015-01-28 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25631615 Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Optic disc area 15,117 European ancestry individuals, 2,131 Erasmus Rucphen Family individuals 2,405 Chinese ancestry individuals, 2,305 Malay ancestry individuals, 2,131 Indian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 10 optic disc area measurement http://www.ebi.ac.uk/efo/EFO_0006937 GCST002765 Genome-wide genotyping array 2015-11-17 25631615 Springelkamp H 2015-01-28 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25631615 Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Optic cup area 15,087 European ancestry individuals, 2,131 Erasmus Rucphen Family individuals, 2,363 Chinese ancestry individuals, 2,225 Malay ancestry individuals, 2,025 Indian ancestry individuals NA Affymetrix, Illumina [2500000] (imputed) 16 optic cup area measurement http://www.ebi.ac.uk/efo/EFO_0006940 GCST002764 Genome-wide genotyping array 2015-11-17 25631615 Springelkamp H 2015-01-28 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25631615 Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Optic cup area 15,087 European ancestry individuals, 2,131 Erasmus Rucphen Family individuals 2,363 Chinese ancestry individuals, 2,225 Malay ancestry individuals, 2,025 Indian ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 30 optic cup area measurement http://www.ebi.ac.uk/efo/EFO_0006940 GCST002762 Genome-wide genotyping array 2015-11-17 25631615 Springelkamp H 2015-01-28 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/25631615 Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology. Optic disc area 15,117 European ancestry individuals, 2,131 Erasmus Rucphen Family individuals, 2,405 Chinese ancestry individuals, 2,305 Malay ancestry individuals, 2,131 Indian ancestry individuals NA Affymetrix, Illumina [2500000] (imputed) 19 optic disc area measurement http://www.ebi.ac.uk/efo/EFO_0006937 GCST002763 Genome-wide genotyping array 2015-10-27 25625606 Mather KA 2015-01-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/25625606 Investigating the genetics of hippocampal volume in older adults without dementia. Hippocampal atrophy 325 European ancestry older adult individuals NA Affymetrix [at least 734550] (imputed) 3 hippocampal atrophy http://www.ebi.ac.uk/efo/EFO_0005039 GCST002760 Genome-wide genotyping array 2015-10-27 25625606 Mather KA 2015-01-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/25625606 Investigating the genetics of hippocampal volume in older adults without dementia. Hippocampal volume 498 European ancestry older adult individuals NA Affymetrix, Illumina [at least 646791] (imputed) 19 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST002761 Genome-wide genotyping array 2015-11-03 25607358 Hibar DP 2015-01-21 Nature www.ncbi.nlm.nih.gov/pubmed/25607358 Common genetic variants influence human subcortical brain structures. Subcortical brain region volumes up to 13,171 European ancestry individuals up to 15,130 European ancestry individuals, 545 Japanese ancestry individuals, 736 Mexican American individuals Affymetrix, Illumina [NR] (imputed) 12 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST002756 Genome-wide genotyping array 2015-12-01 25695618 Chittani M 2015-02-18 J Hypertens www.ncbi.nlm.nih.gov/pubmed/25695618 TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives. Blood pressure response to hydrochlorothiazide in hypertension 485 European ancestry cases 1,545 European ancestry cases Illumina [~ 6000000] (imputed) 0 response to hydrochlorothiazide, diastolic blood pressure change measurement, systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0005202, http://www.ebi.ac.uk/efo/EFO_0006945, http://www.ebi.ac.uk/efo/EFO_0006944 GCST002784 Genome-wide genotyping array 2015-11-13 25823570 Miyake M 2015-03-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25823570 Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. Axial length Up to 3,248 Japanese ancestry individuals 3,460 Japanese ancestry individuals Illumina [1773334] (imputed) 1 axial length measurement http://www.ebi.ac.uk/efo/EFO_0005318 GCST002836 Genome-wide genotyping array 2015-11-12 25823570 Miyake M 2015-03-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25823570 Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia. Corneal curvature Up to 3,248 Japanese ancestry individuals 6,234 East Asian ancestry individuals, 2,007 European ancestry individuals Illumina [1773334] (imputed) 1 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST002834 Genome-wide genotyping array 2015-12-03 25601762 Wang Y 2015-01-20 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/25601762 Pharmacodynamic genome-wide association study identifies new responsive loci for glucocorticoid intervention in asthma. Response to inhaled glucocorticoid treatment in asthma (change in FEV1) 120 individuals 410 individuals Affymetrix [266944] 2 FEV change measurement, response to glucocorticoid http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0051384 GCST002754 Genome-wide genotyping array 2016-02-05 25898920 Korostishevsky M 2015-04-22 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/25898920 Genomics and metabolomics of muscular mass in a community-based sample of UK females. Blood metabolite levels 3,953 European ancestry individuals NA Illumina [2300000] 4 urate measurement, mannose measurement, blood metabolite measurement, X12063 measurement http://www.ebi.ac.uk/efo/EFO_0004531, http://www.ebi.ac.uk/efo/EFO_0006958, http://www.ebi.ac.uk/efo/EFO_0005664, http://www.ebi.ac.uk/efo/EFO_0006957 GCST002872 Genome-wide genotyping array 2015-05-30 25241909 Lee JH 2014-09-21 Respir Res www.ncbi.nlm.nih.gov/pubmed/25241909 Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. Chronic obstructive pulmonary disease 3,777 European ancestry cases, 3,520 European ancestry smoker controls NA Illumina [NR] (imputed) 3 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST002624 Genome-wide genotyping array 2015-06-01 25241909 Lee JH 2014-09-21 Respir Res www.ncbi.nlm.nih.gov/pubmed/25241909 Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. Chronic bronchitis and chronic obstructive pulmonary disease up to 1,662 European ancestry cases, up to 3,520 European ancestry smoker controls, 182 African American cases, 1,749 African American smoker controls NA Illumina [NR] (imputed) 11 chronic obstructive pulmonary disease, chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0000341, http://www.ebi.ac.uk/efo/EFO_0006505 GCST002625 Genome-wide genotyping array 2015-05-30 25241909 Lee JH 2014-09-21 Respir Res www.ncbi.nlm.nih.gov/pubmed/25241909 Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease. Chronic bronchitis in chronic obstructive pulmonary disease 1,662 European ancestry cases, 3,777 European ancestry controls NA Illumina [NR] (imputed) 1 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST002621 Genome-wide genotyping array 2016-01-30 25823687 Cao S 2015-03-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/25823687 Genome-wide association study of myelosuppression in non-small-cell lung cancer patients with platinum-based chemotherapy. Platinum-induced myelosuppression in non-small cell lung cancer 328 Han Chinese ancestry cases 876 Han Chinese ancestry cases Affymetrix [588732] 1 myelosuppression, response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0007053, http://www.ebi.ac.uk/efo/EFO_0004647 GCST002833 Genome-wide genotyping array 2016-01-15 25827505 Swaminathan S 2015-03-14 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/25827505 Characteristics of Bipolar I patients grouped by externalizing disorders. Bipolar disorder 472 non-externalizing cases, 796 externalizing cases 436 non-externalizing European ancestry cases, 801 externalizing European ancestry cases Affymetrix [677171] 4 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST002809 Genome-wide genotyping array 2016-01-27 25673413 Locke AE 2015-02-12 Nature www.ncbi.nlm.nih.gov/pubmed/25673413 Genetic studies of body mass index yield new insights for obesity biology. Body mass index up to 104,666 European ancestry male individuals, up to 132,115 European ancestry female individuals, 370 African American male individuals, 517 African American female individuals, 512 Hispanic male individuals, 764 Hispanic female individuals up to 48,274 European ancestry male individuals, up to 39,864 European ancestry female individuals, 2,441 African American or Afro-Caribbean male individuals, 6,314 African American or Afro-Caribbean female individuals, 919 Filipino male individuals, 828 Filipino female individuals, 205 Seychellois male individuals, 287 Seychellois female individuals, 2,964 South Asian ancestry male individuals, 658 South Asian ancestry female individuals Affymetrix, Illumina [2550021] 634 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST002783 Genome-wide genotyping array 2016-12-05 26965164 Hanchard NA 2016-03-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26965164 A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20. Congenital left-sided heart lesions 592 European ancestry cases, 2,676 European ancestry controls 367 European ancestry cases, 5,159 European ancestry controls Illumina [534461] 2 congenital left-sided heart lesions http://www.ebi.ac.uk/efo/EFO_0005938 GCST003419 Genome-wide genotyping array 2016-11-30 26733130 Styrkarsdottir U 2016-01-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26733130 Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures. Bone mineral density (spine) up to 20,132 European ancestry individuals 10,092 European and East Asian ancestry individuals Illumina [19689642] (imputed) 7 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST003388 Genome-wide genotyping array 2016-11-30 26733130 Styrkarsdottir U 2016-01-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26733130 Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures. Bone mineral density (hip) up to 20,162 European ancestry individuals 10,037 European and East Asian ancestry individuals Illumina [19689642] (imputed) 7 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST003389 Genome-wide genotyping array 2018-11-13 25604533 Renauer PA 2015-01-20 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/25604533 Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome-Wide Association Study. Takayasu arteritis 516 Turkish ancestry cases, 119 European ancestry cases, 462 Turkish ancestry controls, 993 European ancestry controls NA Illumina [up to 547389] 58 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST006575 Genome-wide genotyping array 2015-08-09 25646338 Mozaffarian D 2014-12-10 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/25646338 Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. Trans fatty acid levels 8,013 European ancestry individuals 1,082 African American individuals, 669 Chinese ancestry individuals, 657 Hispanic individuals Affymetrix, Illumina [~ 2500000] (imputed) 131 trans fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0006821 GCST002721 Genome-wide genotyping array 2016-10-07 26718567 Williams SR 2015-12-30 Neurology www.ncbi.nlm.nih.gov/pubmed/26718567 Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. C-reactive protein levels in ischemic stroke up to 1,725 European ancestry cases, up to 258 African ancestry cases, up to 117 cases NA Illumina [7500450] (imputed) 2 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST003211 Genome-wide genotyping array 2016-10-12 26718567 Williams SR 2015-12-30 Neurology www.ncbi.nlm.nih.gov/pubmed/26718567 Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. Thrombomodulin levels in ischemic stroke up to 1,725 European ancestry cases, up to 258 African ancestry cases, up to 117 cases NA Illumina [7500450] (imputed) 7 thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0007774 GCST003234 Genome-wide genotyping array 2016-10-07 26718567 Williams SR 2015-12-30 Neurology www.ncbi.nlm.nih.gov/pubmed/26718567 Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. Creatinine levels in ischemic stroke 1,725 European ancestry cases, 258 African ancestry cases, 117 cases NA Illumina [7500450] (imputed) 6 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST003213 Genome-wide genotyping array 2016-10-12 26718567 Williams SR 2015-12-30 Neurology www.ncbi.nlm.nih.gov/pubmed/26718567 Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. Thrombin-antithrombin complex levels in ischemic stroke up to 1,725 European ancestry cases, up to 258 African ancestry cases, up to 117 cases NA Illumina [7500450] (imputed) 6 thrombin-antithrombin complex measurement http://www.ebi.ac.uk/efo/EFO_0007775 GCST003233 Genome-wide genotyping array 2016-10-07 26718567 Williams SR 2015-12-30 Neurology www.ncbi.nlm.nih.gov/pubmed/26718567 Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. Fibrinogen levels in ischemic stroke up to 1,725 European ancestry cases, up to 258 African ancestry cases, up to 117 cases NA Illumina [7500450] (imputed) 1 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST003212 Genome-wide genotyping array 2016-10-12 26718567 Williams SR 2015-12-30 Neurology www.ncbi.nlm.nih.gov/pubmed/26718567 Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke. Prothrombin fragments F1+2 levels in ischemic stroke up to 1,725 European ancestry cases,up to 258 African ancestry cases, up to 117 cases NA Illumina [7500450] (imputed) 2 prothrombin fragments F1+2 measurement http://www.ebi.ac.uk/efo/EFO_0007776 GCST003235 Genome-wide genotyping array 2016-10-10 26424050 Kinnersley B 2015-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26424050 Genome-wide association study identifies multiple susceptibility loci for glioma. Glioblastoma 1,783 Northern European ancestry cases, 7,435 Northern European ancestry controls up to 1,490 European ancestry cases, up to 1,723 European ancestry controls Illumina [at least 8427548] (imputed) 7 glioblastoma multiforme http://www.ebi.ac.uk/efo/EFO_0000519 GCST003220 Genome-wide genotyping array 2016-10-12 26424050 Kinnersley B 2015-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26424050 Genome-wide association study identifies multiple susceptibility loci for glioma. Non-glioblastoma glioma 2,364 Northern European ancestry cases, 7,435 Northern European ancestry controls up to 1,490 European ancestry cases, up to 1,723 European ancestry controls Illumina [at least 8427548] (imputed) 11 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST003227 Genome-wide genotyping array 2016-10-12 26424050 Kinnersley B 2015-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26424050 Genome-wide association study identifies multiple susceptibility loci for glioma. Glioma 1,783 Northern European ancestry glioblastoma cases, 2,364 Northern European ancestry non-glioblastoma cases, 7,435 Northern European ancestry controls 1,490 European ancestry cases, 1,723 European ancestry control Illumina [at least 8427548] (imputed) 11 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST003228 Genome-wide genotyping array 2016-11-29 26911590 Mullin BH 2016-02-25 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/26911590 Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density. Bone mineral density (spine) 1,042 Northern European ancestry individuals 5,654 Northern European ancestry individuals Illumina [NR] (imputed) 6 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST003380 Genome-wide genotyping array 2016-11-29 26911590 Mullin BH 2016-02-25 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/26911590 Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density. Bone mineral density (hip) 1,042 Northern European ancestry individuals 5,654 Northern European ancestry individuals Illumina [NR] (imputed) 3 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST003379 Genome-wide genotyping array 2016-11-29 26911590 Mullin BH 2016-02-25 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/26911590 Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density. Bone mineral density (femoral neck) 1,042 Northern European ancestry individuals 5,654 Northern European ancestry individuals Illumina [NR] (imputed) 6 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST003381 Genome-wide genotyping array 2015-11-07 25646370 Matsuo H 2015-02-02 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/25646370 Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes. Gout 945 Japanese ancestry cases, 1,213 Japanese ancestry controls 1,048 Japanese ancestry cases, 1,334 Japanese ancestry controls Illumina [570442] 6 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST002773 Genome-wide genotyping array 2016-11-29 26888256 Hernandez W 2016-02-17 Blood www.ncbi.nlm.nih.gov/pubmed/26888256 Novel genetic predictors of venous thromboembolism risk in African Americans. Venous thromboembolism 146 African American cases, 432 African American controls 94 African American cases, 65 African American controls Illumina [10690342] (imputed) 4 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST003377 Genome-wide genotyping array 2016-11-22 26891255 Jung ES 2016-02-18 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/26891255 HLA-C*01 is a Risk Factor for Crohn's Disease. Crohn's disease 275 Korean ancestry cases, 2,369 Korean ancestry controls 242 Korean ancestry cases, 1,066 Korean ancestry controls Affymetrix [3387207] (imputed) 5 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST003360 Genome-wide genotyping array 2016-12-08 26861389 D'Adamo CR 2016-02-06 Nutrients www.ncbi.nlm.nih.gov/pubmed/26861389 A Common Variant in the SETD7 Gene Predicts Serum Lycopene Concentrations. Serum lycopene concentrations 441 Old Order Amish individuals from 308 families NA Affymetrix [2302013] (imputed) 5 lycopene measurement http://www.ebi.ac.uk/efo/EFO_0007801 GCST003433 Genome-wide genotyping array 2016-12-01 26908601 Hinds DA 2016-02-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26908601 Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis. Thrombosis 6,135 European ancestry cases, 252,827 European ancestry controls NA Illumina [at least 560000] (imputed) 13 Ischemic stroke, venous thromboembolism, stroke, Abnormal thrombosis, deep vein thrombosis, pulmonary embolism http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0000712, http://purl.obolibrary.org/obo/HP_0001977, http://www.ebi.ac.uk/efo/EFO_0003907, http://www.ebi.ac.uk/efo/EFO_0003827 GCST003390 Genome-wide genotyping array 2016-11-16 26732429 Wang Z 2016-01-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26732429 Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women. Lung cancer 6,877 East Asian ancestry never smoker cases, 6,277 East Asian ancestry never smoker controls 5,878 East Asian ancestry never smoker cases, 7,046 East Asian ancestry never smoker controls Affymetrix, Illumina [7564751] (imputed) 6 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST003325 Genome-wide genotyping array 2016-11-16 26732429 Wang Z 2016-01-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/26732429 Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women. Adenocarcinoma Up to 5,744 Chinese ancestry cases, up to 4,817 Chinese ancestry controls, up to 1,133 Japanese ancestry cases, up to 1,460 Japanese ancestry controls Up to 4,647 Chinese ancestry cases, up to 4,099 Chinese ancestry controls, up to 1,231 Japanese ancestry cases, up to 2,947 Japanese ancestry controls Affymetrix, Illumina [7564751] (imputed) 5 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST003326 Genome-wide genotyping array 2016-11-25 26833098 Kilpelainen TO 2016-02-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26833098 Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. circulating leptin levels adjusted for BMI up to 14,094 European ancestry men, up to 19,893 European ancestry women up to 9,076 European ancestry men, up to 9,150 European ancestry women Affymetrix, Illumina [~ 2500000] (imputed) 9 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST003368 Genome-wide genotyping array 2016-11-25 26833098 Kilpelainen TO 2016-02-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26833098 Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels. circulating leptin levels 14,586 European ancestry men, 20,706 European ancestry women 8,554 European ancestry men, 8,337 European ancestry women Affymetrix, Illumina [~ 2500000] (imputed) 10 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST003367 Genome-wide genotyping array 2016-12-14 26741287 Milet J 2016-01-07 Genes Immun www.ncbi.nlm.nih.gov/pubmed/26741287 Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens. IgG1 response to Plasmodium falciparum antigen (GLURP) 528 Sereer ancestry individuals from 130 families NA Affymetrix [174950] 1 Plasmodium falciparum antigen IgG1 measurement http://www.ebi.ac.uk/efo/EFO_0007810 GCST003460 Genome-wide genotyping array 2016-12-14 26741287 Milet J 2016-01-07 Genes Immun www.ncbi.nlm.nih.gov/pubmed/26741287 Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens. IgG response to Plasmodium falciparum antigens (GLURP, MSP2 FC27, MSP2 3D7) 528 Sereer ancestry individuals from 130 families NA Affymetrix [174950] 2 Plasmodium falciparum antigen IgG measurement http://www.ebi.ac.uk/efo/EFO_0007812 GCST003461 Genome-wide genotyping array 2016-12-14 26741287 Milet J 2016-01-07 Genes Immun www.ncbi.nlm.nih.gov/pubmed/26741287 Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens. IgG1 response to Plasmodium falciparum antigen (MSP1) 528 Sereer ancestry individuals from 130 individuals NA Affymetrix [174950] 0 Plasmodium falciparum antigen IgG1 measurement http://www.ebi.ac.uk/efo/EFO_0007810 GCST003462 Genome-wide genotyping array 2016-12-14 26741287 Milet J 2016-01-07 Genes Immun www.ncbi.nlm.nih.gov/pubmed/26741287 Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens. IgG3 response to Plasmodium falciparum antigen (MSP2 3D7) 528 Sereer ancestry individuals from 130 families NA Affymetrix [174950] 0 Plasmodium falciparum antigen IgG3 measurement http://www.ebi.ac.uk/efo/EFO_0007811 GCST003463 Genome-wide genotyping array 2016-12-14 26741287 Milet J 2016-01-07 Genes Immun www.ncbi.nlm.nih.gov/pubmed/26741287 Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens. IgG3 response to Plasmodium falciparum antigen (MSP2 FC27) 528 Sereer ancestry individuals from 130 families NA Affymetrix [174950] 0 Plasmodium falciparum antigen IgG3 measurement http://www.ebi.ac.uk/efo/EFO_0007811 GCST003464 Genome-wide genotyping array 2016-10-14 26626624 Stuart PE 2015-11-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26626624 Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. Cutaneous psoriasis 1,363 European ancestry cases, 4,934 European ancestry controls up to 2,969 European ancestry cases, up to European ancestry 14,384 controls Illumina [11532644] (imputed) 10 cutaneous psoriasis measurement, psoriasis http://www.ebi.ac.uk/efo/EFO_0007773, http://www.ebi.ac.uk/efo/EFO_0000676 GCST003269 Genome-wide genotyping array 2016-10-14 26626624 Stuart PE 2015-11-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26626624 Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. Psoriasis vulgaris 4,007 European ancestry cases, 4,934 European ancestry controls up to 9,075 European ancestry cases, up to European ancestry 12,726 controls Illumina [up to 11532644] (imputed) 39 psoriasis vulgaris http://www.ebi.ac.uk/efo/EFO_1001494 GCST003268 Genome-wide genotyping array 2016-10-14 26626624 Stuart PE 2015-11-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26626624 Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. Psoriatic arthritis 1,946 European ancestry cases, 4,934 European ancestry controls up to 2,883 European ancestry cases, up to 14,179 European ancestry controls Illumina [11532644] (imputed) 14 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST003270 Genome-wide genotyping array 2016-10-14 26626624 Stuart PE 2015-11-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26626624 Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture. Psoriatic arthritis vs Cutaneous psoriasis 1,946 European ancestry psoriatic arthritis cases, 1,363 European ancestry cuteneous psoriasis cases up to 3,216 European ancestry psoriatic arthritis cases, up to 2,968 European ancestry cuteneous psoriasis cases Illumina [11532644] (imputed) 0 cutaneous psoriasis measurement, psoriatic arthritis, psoriasis http://www.ebi.ac.uk/efo/EFO_0007773, http://www.ebi.ac.uk/efo/EFO_0003778, http://www.ebi.ac.uk/efo/EFO_0000676 GCST003271 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Plasma omega-3 polyunsaturated fatty acid level (eicosapentaenoic acid) 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 13 eicosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007760 GCST003241 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Plasma omega-3 polyunsaturated fatty acid levels (docosahexaenoic acid) 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 18 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST003240 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Plasma omega-6 polyunsaturated fatty acid levels (linoleic acid) 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 20 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST003239 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Plasma omega-6 polyunsaturated fatty acid levels (gamma-linolenic acid) 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 15 gamma-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007762 GCST003238 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Plasma omega-6 polyunsaturated fatty acid levels (dihomo-gamma-linolenic acid) 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 13 dihomo-gamma-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007763 GCST003237 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Plasma omega-6 polyunsaturated fatty acid levels (arachidonic acid) 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 20 arachidonic acid measurement http://www.ebi.ac.uk/efo/EFO_0006808 GCST003236 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Delta-5 desaturase activity 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 10 delta-5 desaturase measurement http://www.ebi.ac.uk/efo/EFO_0007764 GCST003243 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Delta-6 desaturase activity 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 10 delta-6 desaturase measurement http://www.ebi.ac.uk/efo/EFO_0007765 GCST003244 Genome-wide genotyping array 2016-10-12 26584805 Dorajoo R 2015-11-19 Genes Nutr www.ncbi.nlm.nih.gov/pubmed/26584805 A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population. Plasma omega-3 polyunsaturated fatty acid levels (alphalinolenic acid) 717 Singaporean Chinese ancestry myocardial infarction cases, 644 Singaporean Chinese ancestry controls NA Illumina [up to 1980188] (imputed) 11 alpha-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007759 GCST003242 Genome-wide genotyping array 2016-12-07 26913989 Traylor M 2016-02-23 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/26913989 Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease. Alzheimer's disease or small vessel stroke 17,008 European ancestry Alzheimer's disease cases, 3,651 European ancestry small vessel stroke cases, 95,811 European ancestry controls NA Affymetrix, Illumina [at least 7055881] 1 Alzheimer disease, small vessel stroke http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_1001504 GCST003423 Genome-wide genotyping array 2016-11-22 26902266 Giri AK 2016-02-23 Sci Rep www.ncbi.nlm.nih.gov/pubmed/26902266 Genome wide association study of uric acid in Indian population and interaction of identified variants with Type 2 diabetes. Serum uric acid levels 1,109 Indo-European ancestry individuals 3,725 Indo-European ancestry individuals Illumina [539662] 5 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST003359 Genome-wide genotyping array 2016-11-16 26732560 Cheng YC 2016-01-05 Stroke www.ncbi.nlm.nih.gov/pubmed/26732560 Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. Ischemic stroke 2,567 European ancestry cases, 17,163 European ancestry controls, 381 African American ancestry cases, 352 African American ancestry controls, 678 Pakistani ancestry cases, 4,453 Pakistani ancestry controls 1,003 European ancestry cases, 7,745 European ancestry controls Illumina [up to 13439215] (imputed) 4 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST003324 Genome-wide genotyping array 2016-11-16 26732560 Cheng YC 2016-01-05 Stroke www.ncbi.nlm.nih.gov/pubmed/26732560 Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. Ischemic stroke (large artery atherosclerosis) 401 European ancestry cases, 17,164 European ancestry controls, 23 African American ancestry cases, 352 African American ancestry controls, 257 Pakistani ancestry cases, 4,453 Pakistani ancestry controls NA Illumina [up to 13439215] (imputed) 3 Ischemic stroke, large artery stroke http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0005524 GCST003322 Genome-wide genotyping array 2016-11-16 26732560 Cheng YC 2016-01-05 Stroke www.ncbi.nlm.nih.gov/pubmed/26732560 Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. Ischemic stroke (undetermined subtype) 1,022 European ancestry cases, 17,164 European ancestry controls, 183 African American ancestry cases, 352 African American ancestry controls, 754 Pakistani ancestry cases, 4,453 Pakistani ancestry controls NA Illumina [up to 13439215] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST003320 Genome-wide genotyping array 2016-11-16 26732560 Cheng YC 2016-01-05 Stroke www.ncbi.nlm.nih.gov/pubmed/26732560 Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. Ischemic stroke (cardioembolic) 552 European ancestry cases, 17,164 European ancestry controls, 74 African American ancestry cases, 352 African American ancestry controls, 293 Pakistani ancestry cases, 4,453 Pakistani ancestry controls NA Illumina [up to 13439215] (imputed) 0 Ischemic stroke, cardiac embolism http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_1001493 GCST003323 Genome-wide genotyping array 2016-11-16 26732560 Cheng YC 2016-01-05 Stroke www.ncbi.nlm.nih.gov/pubmed/26732560 Genome-Wide Association Analysis of Young-Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2. Small vessel stroke 292 European ancestry cases, 17,164 European ancestry controls, 77 African American ancestry cases, 352 African American ancestry controls, 232 Pakistani ancestry cases, 4,453 Pakistani ancestry controls NA Illumina [up to 13439215] (imputed) 1 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST003321 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Entorhinal cortical thickness 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 5 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST000894 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Entorhinal cortical volume 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 1 entorhinal cortical volume http://www.ebi.ac.uk/efo/EFO_0005092 GCST000899 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Whole-brain volume 434 European ancestry mild cognitive impairment cases, 245 European ancestry Alzheimer's disease cases, 284 European ancestry controls NA Illumina [478011] 4 whole-brain volume http://www.ebi.ac.uk/efo/EFO_0005089 GCST000891 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Hippocampal volume 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 3 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST000890 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Entorhinal cortical thickness (Alzheimer's disease interaction) 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 1 Alzheimer disease, cortical thickness http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004840 GCST000889 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Total ventricular volume 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 8 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST000898 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Entorhinal cortical volume (Alzheimer's disease interaction) 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 1 Alzheimer disease, entorhinal cortical volume http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0005092 GCST000893 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Total ventricular volume (Alzheimer's disease interaction) 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 11 Alzheimer disease, brain volume measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0006930 GCST000892 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Whole-brain volume (Alzheimer's disease interaction) 434 European ancestry mild cognitive impairment cases, 245 European ancestry Alzheimer's disease cases, 284 European ancestry controls NA Illumina [478011] 4 Alzheimer disease, whole-brain volume http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0005089 GCST000895 Genome-wide genotyping array 2016-03-24 21116278 Furney SJ 2010-11-30 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/21116278 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. Hippocampal volume (Alzheimer's disease interaction) 424 European ancestry mild cognitive impairment cases, 236 European ancestry Alzheimer's disease cases, 279 European ancestry controls NA Illumina [478011] 0 Alzheimer disease, hippocampal volume http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0005035 GCST000897 Genome-wide genotyping array 2021-02-03 32733355 Ryu HS 2020-07-07 Front Neurol www.ncbi.nlm.nih.gov/pubmed/32733355 Genomic Analysis Identifies New Loci Associated With Motor Complications in Parkinson's Disease. Motor fluctuations in levodopa treated Parkinson's disease 219 Korean ancestry cases, 522 Korean ancestry controls NA Affymetrix [583535] (imputed) 4 motor function measurement, response to levodopa http://www.ebi.ac.uk/efo/EFO_0010749, http://www.ebi.ac.uk/efo/EFO_0010747 GCST011066 Genome-wide genotyping array 2021-02-03 32733355 Ryu HS 2020-07-07 Front Neurol www.ncbi.nlm.nih.gov/pubmed/32733355 Genomic Analysis Identifies New Loci Associated With Motor Complications in Parkinson's Disease. Levodopa-induced dyskinesia in levodopa treated Parkinson's disease 172 Korean ancestry cases, 569 Korean ancestry controls NA Affymetrix [583535] (imputed) 12 drug-Induced dyskinesia, response to levodopa http://www.ebi.ac.uk/efo/EFO_1000904, http://www.ebi.ac.uk/efo/EFO_0010747 GCST011065 Genome-wide genotyping array 2021-02-25 32722627 Jin T 2020-07-26 Nutrients www.ncbi.nlm.nih.gov/pubmed/32722627 Interactions of Habitual Coffee Consumption by Genetic Polymorphisms with the Risk of Prediabetes and Type 2 Diabetes Combined. Coffee consumption 6,080 Korean ancestry cases, 1,788 Korean ancestry controls NA Affymetrix [352228] (imputed) 11 coffee consumption http://www.ebi.ac.uk/efo/EFO_0004330 GCST011158 Genome-wide genotyping array 2020-09-10 32742401 Parviainen R 2020-06-12 Exp Ther Med www.ncbi.nlm.nih.gov/pubmed/32742401 A single genetic locus associated with pediatric fractures: A genome-wide association study on 3,230 patients. Fractures (paediatric) 48 European ancestry cases, 3,182 European ancestry controls NA Illumina [3515000] (imputed) 7 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST010516 Genome-wide genotyping array 2021-06-08 32491161 Chu BB 2020-06-01 Gigascience www.ncbi.nlm.nih.gov/pubmed/32491161 Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity. Hypertension 185,565 European ancestry individuals NA NR [470228] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST011824 Genome-wide genotyping array 2021-06-08 32491161 Chu BB 2020-06-01 Gigascience www.ncbi.nlm.nih.gov/pubmed/32491161 Iterative hard thresholding in genome-wide association studies: Generalized linear models, prior weights, and double sparsity. High density lipoprotein cholesterol levels 5,402 individuals NA NR [364590] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST011825 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red blood cell count 8,189 South Asian ancestry individuals NA Affymetrix, Illumina [28493162] (imputed) 5 red blood cell density measurement http://www.ebi.ac.uk/efo/EFO_0007978 GCST90002366 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red blood cell count 727,624 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [24332387] (imputed) 449 red blood cell density measurement http://www.ebi.ac.uk/efo/EFO_0007978 GCST90002367 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red cell distribution width 13,519 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36660117] (imputed) 5 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90002368 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red cell distribution width 531,774 European ancestry individuals NA Affymetrix, Illumina [49860007] (imputed) 385 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90002369 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red cell distribution width 8,526 Hispanic or Latin American individuals NA Affymetrix, Illumina [26792043] (imputed) 2 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90002370 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red cell distribution width 8,166 South Asian ancestry individuals NA Affymetrix, Illumina [28471494] (imputed) 5 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90002371 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red cell distribution width 563,352 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [22063850] (imputed) 340 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90002372 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. White blood cell count 15,061 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36864690] (imputed) 22 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90002373 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. White blood cell count 562,243 European ancestry individuals NA Affymetrix, Illumina [50601830] (imputed) 478 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90002374 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. White blood cell count 151,807 East Asian ancestry individuals NA Affymetrix, Illumina [16710636] (imputed) 38 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90002375 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. White blood cell count 9,368 Hispanic or Latin American individuals NA Affymetrix, Illumina [26925380] (imputed) 4 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90002376 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. White blood cell count 8,188 South Asian ancestry individuals NA Affymetrix, Illumina [28492541] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90002377 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. White blood cell count 746,667 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [24649327] (imputed) 443 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90002378 Genome-wide genotyping array 2021-05-24 32653958 Cho HW 2020-07-11 J Bone Miner Metab www.ncbi.nlm.nih.gov/pubmed/32653958 Association between non-Caucasian-specific ASCC1 gene polymorphism and osteoporosis and obesity in Korean postmenopausal women. Body mass index 3,013 Korean ancestry individuals NA Affymetrix [NR] 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST011717 Genome-wide genotyping array 2021-05-24 32653958 Cho HW 2020-07-11 J Bone Miner Metab www.ncbi.nlm.nih.gov/pubmed/32653958 Association between non-Caucasian-specific ASCC1 gene polymorphism and osteoporosis and obesity in Korean postmenopausal women. Osteoporosis 443 Korean ancestry cases, 2,223 Korean ancestry controls NA Affymetrix [NR] 5 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST011716 Genome-wide genotyping array 2021-03-24 32716492 Simcoe MJ 2020-07-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/32716492 Genome-wide association study of corneal biomechanical properties identifies over 200 loci providing insight into the genetic aetiology of ocular diseases. Corneal hysteresis 106,041 European ancestry individuals 9,029 European ancestry individuals Affymetrix [12000000] (imputed) 11 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST011391 Genome-wide genotyping array 2021-03-24 32716492 Simcoe MJ 2020-07-27 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/32716492 Genome-wide association study of corneal biomechanical properties identifies over 200 loci providing insight into the genetic aetiology of ocular diseases. Corneal resistance factor 106,030 European ancestry individuals 9,029 European ancestry individuals Affymetrix [12000000] (imputed) 13 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST011390 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Monocyte count 88,929 East Asian ancestry individuals NA Affymetrix, Illumina [16289044] (imputed) 34 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90002341 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Monocyte count 7,543 Hispanic or Latin American individuals NA Affymetrix, Illumina [25652698] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90002342 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Monocyte count 7,043 South Asian ancestry individuals NA Affymetrix, Illumina [28465834] (imputed) 3 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90002343 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Monocyte count 639,696 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [23467995] (imputed) 394 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90002344 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean platelet volume 10,737 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36042313] (imputed) 13 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90002345 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean platelet volume 460,935 European ancestry individuals NA Affymetrix, Illumina [49660172] (imputed) 423 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90002346 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean platelet volume 2,810 Hispanic or Latin American individuals NA Affymetrix, Illumina [24878602] (imputed) 3 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90002347 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean platelet volume 8,189 South Asian ancestry individuals NA Affymetrix, Illumina [28493265] (imputed) 11 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90002348 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean platelet volume 484,042 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [17210439] (imputed) 392 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90002349 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Neutrophil count 13,476 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36456987] (imputed) 21 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90002350 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Neutrophil count 519,288 European ancestry individuals NA Affymetrix, Illumina [50250472] (imputed) 397 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90002351 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Neutrophil count 78,744 East Asian ancestry individuals NA Affymetrix, Illumina [16289093] (imputed) 17 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90002352 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Neutrophil count 7,542 Hispanic or Latin American individuals NA Affymetrix, Illumina [25652697] (imputed) 5 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90002353 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Neutrophil count 8,165 South Asian ancestry individuals NA Affymetrix, Illumina [28471362] (imputed) 1 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90002354 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Neutrophil count 627,215 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [23114412] (imputed) 352 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90002355 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Platelet count 15,171 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36877391] (imputed) 9 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90002356 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Platelet count 542,827 European ancestry individuals NA Affymetrix, Illumina [50241410] (imputed) 556 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90002357 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Platelet count 145,648 East Asian ancestry individuals NA Affymetrix, Illumina [16710488] (imputed) 81 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90002358 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Platelet count 9,367 Hispanic or Latin American individuals NA Affymetrix, Illumina [26925389] (imputed) 2 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90002359 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Platelet count 8,188 South Asian ancestry individuals NA Affymetrix, Illumina [28492373] (imputed) 4 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90002360 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Platelet count 721,201 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [24588908] (imputed) 552 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90002361 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red blood cell count 14,222 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36679691] (imputed) 3 red blood cell density measurement http://www.ebi.ac.uk/efo/EFO_0007978 GCST90002362 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red blood cell count 545,203 European ancestry individuals NA Affymetrix, Illumina [50628390] (imputed) 497 red blood cell density measurement http://www.ebi.ac.uk/efo/EFO_0007978 GCST90002363 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red blood cell count 150,708 East Asian ancestry individuals NA Affymetrix, Illumina [16709798] (imputed) 59 red blood cell density measurement http://www.ebi.ac.uk/efo/EFO_0007978 GCST90002364 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Red blood cell count 9,302 Hispanic or Latin American individuals NA Affymetrix, Illumina [26810348] (imputed) 3 red blood cell density measurement http://www.ebi.ac.uk/efo/EFO_0007978 GCST90002365 Genome-wide genotyping array 2021-02-03 32603185 Ibi D 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32603185 Genome-wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in Hepatic Lipase (LIPC). Fasting triglyceride levels 5,630 individuals NA Illumina [NR] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011052 Genome-wide genotyping array 2021-02-03 32603185 Ibi D 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32603185 Genome-wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in Hepatic Lipase (LIPC). Postprandial triglyceride levels 5,630 individuals NA Illumina [NR] (imputed) 6 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011051 Genome-wide genotyping array 2021-02-03 32603185 Ibi D 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32603185 Genome-wide Association Study of the Postprandial Triglyceride Response Yields Common Genetic Variation in Hepatic Lipase (LIPC). Postprandial triglyceride response 5,630 individuals NA Illumina [NR] (imputed) 7 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011050 Genome-wide genotyping array 2021-01-26 32603359 Ferreira MAR 2020-06-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32603359 Age-of-onset information helps identify 76 genetic variants associated with allergic disease. Allergic disease (asthma, hay fever and/or eczema) (age of onset) 117,130 European ancestry individuals NA NR [7647814] (imputed) 53 age of onset of allergic disease http://purl.obolibrary.org/obo/OBA_2001017 GCST010985 Genome-wide genotyping array 2021-01-26 32603359 Ferreira MAR 2020-06-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32603359 Age-of-onset information helps identify 76 genetic variants associated with allergic disease. Allergic disease (asthma, hay fever and/or eczema) (multivariate analysis) 477,968 European ancestry individuals NA NR [NR] (imputed) 52 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST010984 Genome-wide genotyping array 2020-06-22 23727859 Ellinghaus D 2013-06-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/23727859 High-density genotyping study identifies four new susceptibility loci for atopic dermatitis. Atopic dermatitis 2,425 European ancestry cases, 5,449 European ancestry controls 1,951 European ancestry cases, 4,599 European ancestry controls Illumina [128830] 9 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST010090 Targeted genotyping array [ImmunoChip] 2021-03-22 32741009 Guenther F 2020-08-02 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32741009 Chances and challenges of machine learning-based disease classification in genetic association studies illustrated on age-related macular degeneration. Age-related macular degeneration 3,544 European ancestry cases, 44,521 European ancestry controls NA Affymetrix [11567158] (imputed) 3 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST011317 Genome-wide genotyping array 2021-02-09 32678081 Timmers PRHJ 2020-07-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32678081 Multivariate genomic scan implicates novel loci and haem metabolism in human ageing. Aging traits (healthspan, parental lifespan or longevity) (multivariate analysis) at least 837,415 European ancestry individuals NA NR [7320282] 24 longevity, healthspan, parental longevity http://www.ebi.ac.uk/efo/EFO_0004300, http://www.ebi.ac.uk/efo/EFO_0009762, http://www.ebi.ac.uk/efo/EFO_0007796 GCST011100 Genome-wide genotyping array 2021-06-03 33009551 Zhang J 2020-10-03 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/33009551 Genome-Wide Association Analysis of Neonatal White Matter Microstructure. Neonatal white matter microstructure 471 European, Black, Asian, Native American or unknown ancestry individuals NA Affymetrix [NR] (imputed) 15 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST011780 Genome-wide genotyping array 2020-09-10 32514006 Cho SK 2020-06-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32514006 Polygenic analysis of the effect of common and low-frequency genetic variants on serum uric acid levels in Korean individuals. Serum uric acid levels 6,881 Korean ancestry individuals 3,914 Korean ancestry individuals Affymetrix, Illumina [6129701] (imputed) 34 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST010512 Genome-wide genotyping array 2020-09-21 32518416 Dawoud AAZ 2020-06-10 Leukemia www.ncbi.nlm.nih.gov/pubmed/32518416 Clonal myelopoiesis in the UK Biobank cohort: ASXL1 mutations are strongly associated with smoking. Myeloid clonal hematopoiesis 1,166 cases, 30,892 controls NA Affymetrix [265112] 7 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST010596 Genome-wide genotyping array 2020-09-16 32581359 Saevarsdottir S 2020-06-24 Nature www.ncbi.nlm.nih.gov/pubmed/32581359 FLT3 stop mutation increases FLT3 ligand level and risk of autoimmune thyroid disease. Autoimmune thyroid disease 30,234 European ancestry cases, 724,172 European ancestry controls NA Affymetrix, Illumina [42900000] (imputed) 99 autoimmune thyroid disease http://www.ebi.ac.uk/efo/EFO_0006812 GCST010571 Genome-wide genotyping array, Genome-wide sequencing 2021-05-10 32554045 Rao S 2020-06-15 Gene www.ncbi.nlm.nih.gov/pubmed/32554045 Genome-wide copy number variation-, validation- and screening study implicates a new copy number polymorphism associated with suicide attempts in major depressive disorder. Suicide attempts in major depressive disorder 43 Chinese ancestry cases, 43 Chinese ancestry controls 74 Chinese ancestry cases, 127 Chinese ancestry controls Illumina [745680] 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST011636 Genome-wide genotyping array 2021-01-27 32534018 Liu X 2020-06-10 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32534018 Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study. Mental disorder 43,902 Danish ancestry cases, 19,790 Danish ancestry controls NA NR [7721839] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST011006 Genome-wide genotyping array 2021-01-27 32534018 Liu X 2020-06-10 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32534018 Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study. Autoimmune disease (without mental disorder) 347 Danish ancestry cases, 62,656 Danish ancestry controls NA NR [7721839] (imputed) 0 autoimmune disease http://www.ebi.ac.uk/efo/EFO_0005140 GCST011005 Genome-wide genotyping array 2021-01-27 32534018 Liu X 2020-06-10 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32534018 Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study. Autoimmune traits 1,383 Danish ancestry cases, 62,656 Danish ancestry controls NA NR [7721839] (imputed) 12 autoimmune disease http://www.ebi.ac.uk/efo/EFO_0005140 GCST011008 Genome-wide genotyping array 2021-01-27 32534018 Liu X 2020-06-10 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32534018 Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study. Mental disorder (without autoimmune disease) 42,866 Danish ancestry cases, 19,790 Danish ancestry controls NA NR [7721839] (imputed) 3 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST011007 Genome-wide genotyping array 2021-01-27 32534018 Liu X 2020-06-10 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/32534018 Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study. Autoimmune disease and mental disorder 1,036 Danish ancestry cases, 19,790 Danish ancestry controls NA NR [7721839] (imputed) 1 mental or behavioural disorder, autoimmune disease http://www.ebi.ac.uk/efo/EFO_0000677, http://www.ebi.ac.uk/efo/EFO_0005140 GCST011009 Genome-wide genotyping array 2021-06-14 32538071 Chen Y 2020-06-15 Chem Res Toxicol www.ncbi.nlm.nih.gov/pubmed/32538071 Metabolism and toxicity of emodin: Genome-wide association studies reveal hepatocyte nuclear factor 4α regulates UGT2B7 and emodin glucuronidation. emodin-3-G formation rate 36 individuals NA Illumina [687188] 0 emodin glucuronidation measurement http://www.ebi.ac.uk/efo/EFO_0600010 GCST011857 Genome-wide genotyping array 2021-06-25 33034629 Khoury S 2020-10-09 Sleep www.ncbi.nlm.nih.gov/pubmed/33034629 Multi-ethnic GWAS and meta-analysis of sleep quality identify MPP6 as a novel gene that functions in sleep center neurons. Sleep quality 1,676 non-Hispanic white individuals, 740 African American individuals, 146 Hispanic individuals, 306 individuals 158,207 European ancestry individuals, 16,000 Hispanic individuals, 5,151 African American individuals Illumina [35000000] (imputed) 0 sleep quality http://www.ebi.ac.uk/efo/EFO_0005272 GCST011976 Genome-wide genotyping array 2021-07-09 32814349 Jager R 2020-08-19 Blood www.ncbi.nlm.nih.gov/pubmed/32814349 Germline Genetic Factors Influence Outcome of Interferon Alpha Therapy in Polycythemia Vera. response to ropeginterferon alfa-2b in polycythemia vera 122 individuals 27 individuals Affymetrix [NR] 0 response to ropeginterferon alfa-2b http://www.ebi.ac.uk/efo/EFO_0600013 GCST012018 Genome-wide genotyping array 2020-08-27 32445792 Bani-Fatemi A 2020-05-20 Neurosci Lett www.ncbi.nlm.nih.gov/pubmed/32445792 Genome-wide association study of aggression and violence in schizophrenia. Physical aggression in schizophrenia 205 individuals NA Illumina [NR] 1 aggressive behavior http://www.ebi.ac.uk/efo/EFO_0003015 GCST010467 Genome-wide genotyping array 2020-08-27 32445792 Bani-Fatemi A 2020-05-20 Neurosci Lett www.ncbi.nlm.nih.gov/pubmed/32445792 Genome-wide association study of aggression and violence in schizophrenia. Verbal aggression in schizophrenia 205 individuals NA Illumina [NR] 2 aggressive behavior http://www.ebi.ac.uk/efo/EFO_0003015 GCST010466 Genome-wide genotyping array 2020-08-27 32445792 Bani-Fatemi A 2020-05-20 Neurosci Lett www.ncbi.nlm.nih.gov/pubmed/32445792 Genome-wide association study of aggression and violence in schizophrenia. Aggression against property in schizophrenia 205 individuals NA Illumina [NR] 0 aggressive behavior http://www.ebi.ac.uk/efo/EFO_0003015 GCST010465 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota alpha diversity (Chao1 index) 541 Japanese ancestry women NA Illumina [545605] 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007012 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota alpha diversity (Chao1 index) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 17 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST010819 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota alpha diversity (PD_whole_tree index) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 24 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST010818 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota alpha diversity (Shannon index) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST010817 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota beta diversity (weighted UniFrac distance) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST010816 Genome-wide genotyping array 2020-09-21 32546850 Campos AI 2020-06-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32546850 Genetic aetiology of self-harm ideation and behaviour. Deliberate self-harm 6,872 European ancestry cases, 150,008 European ancestry controls NA Affymetrix [NR] (imputed) 1 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST010603 Genome-wide genotyping array 2020-09-21 32546850 Campos AI 2020-06-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32546850 Genetic aetiology of self-harm ideation and behaviour. Self-harm ideation 23,192 European ancestry cases, 133,524 European ancestry controls NA Affymetrix [NR] (imputed) 1 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST010602 Genome-wide genotyping array 2020-08-26 32438682 Mateos MK 2020-05-19 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/32438682 Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children. Childhood ALL/LBL (acute lymphoblastic leukemia/lymphoblastic lymphoma) treatment-related venous thromboembolism 92 European ancestry cases, 1,481 European ancestry controls NA Illumina [NR] (imputed) 26 venous thromboembolism, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0004286, http://purl.obolibrary.org/obo/GO_0097327 GCST010463 Genome-wide genotyping array 2020-11-06 32562552 Chua KC 2020-06-20 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32562552 Genome-Wide Meta-Analysis Validates a Roless for S1PR1 in Microtubule Targeting Agent-Induced Sensory Peripheral Neuropathy. Sensory peripheral neuropathy in microtubule targeting agent-treated breast cancer 1,324 European ancestry individuals NA Illumina [6030476] (imputed) 18 peripheral neuropathy, response to antimicrotubule agent http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0005260 GCST010732 Genome-wide genotyping array 2020-10-13 32558222 Okamura K 2020-06-18 Pigment Cell Melanoma Res www.ncbi.nlm.nih.gov/pubmed/32558222 Genome-wide association study identifies CDH13 as a susceptibility gene for rhododendrol-induced leukoderma. Leukoderma in response to rhododendrol 147 Japanese ancestry cases, 112 Japanese ancestry controls NA Illumina [1057565] 10 Vitiligo, response to rhododendrol http://www.ebi.ac.uk/efo/EFO_0004208, http://www.ebi.ac.uk/efo/EFO_0010824 GCST010676 Genome-wide genotyping array 2020-09-15 32555152 Smith RL 2020-06-19 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32555152 Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits. Clozapine concentration in schizophrenia 3,473 European ancestry individuals NA Illumina [up to 6200000] (imputed) 1 serum clozapine measurement http://www.ebi.ac.uk/efo/EFO_0600041 GCST010565 Genome-wide genotyping array 2020-09-15 32555152 Smith RL 2020-06-19 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32555152 Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits. N-desmethylclozapine concentration in schizophrenia 3,473 European ancestry individuals NA Illumina [up to 6200000] (imputed) 2 serum N-desmethylclozapine measurement http://www.ebi.ac.uk/efo/EFO_0600043 GCST010564 Genome-wide genotyping array 2020-09-15 32555152 Smith RL 2020-06-19 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32555152 Identification of a novel polymorphism associated with reduced clozapine concentration in schizophrenia patients-a genome-wide association study adjusting for smoking habits. Clozapine-to-N-desmethylclozapine metabolic ratio in schizophrenia 3,473 European ancestry individuals NA Illumina [up to 6200000] (imputed) 2 serum clozapine-to-N-desmethylclozapine ratio measurement http://www.ebi.ac.uk/efo/EFO_0600042 GCST010563 Genome-wide genotyping array 2020-09-14 32451486 Zhou H 2020-05-25 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/32451486 Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. Alcohol use disorder 57,564 European ancestry cases, 256,395 European ancestry controls NA Affymetrix [7003540] (imputed) 26 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST010545 Genome-wide genotyping array 2020-09-14 32451486 Zhou H 2020-05-25 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/32451486 Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. Problematic alcohol use (MTAG) 972,915 European ancestry individuals NA Affymetrix [10613246] (imputed) 76 alcohol use disorder measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0009458, http://www.ebi.ac.uk/efo/EFO_0007878 GCST010544 Genome-wide genotyping array 2020-09-14 32451486 Zhou H 2020-05-25 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/32451486 Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. Alcohol consumption (drinks per week) (MTAG) 972,915 European ancestry individuals NA Affymetrix [NR] (imputed) 86 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST010543 Genome-wide genotyping array 2020-09-14 32451486 Zhou H 2020-05-25 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/32451486 Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. Problematic alcohol use 435,563 European ancestry individuals NA Affymetrix [14069427] (imputed) 32 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST010546 Genome-wide genotyping array 2019-04-09 27548383 Ortiz-Fernandez L 2016-08-22 PLoS One www.ncbi.nlm.nih.gov/pubmed/27548383 Genetic Analysis with the Immunochip Platform in Behçet Disease. Identification of Residues Associated in the HLA Class I Region and New Susceptibility Loci. Behcet's disease 278 Spanish ancestry cases, 1,517 Spanish ancestry controls up to 130 Spanish ancestry cases, up to 605 Spanish ancestry controls Illumina [133018] 3 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST007551 Targeted genotyping array [ImmunoChip] 2021-04-28 32944759 Deshmukh HA 2020-09-18 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/32944759 Genome-Wide Association Analysis of Pancreatic Beta Cell Glucose Sensitivity. Pancreatic beta-cell glucose sensitivity 3,017 European ancestry individuals 2,689 European ancestry individuals Illumina [8978282] (imputed) 9 diabetes mellitus biomarker http://www.ebi.ac.uk/efo/EFO_0006842 GCST011569 Genome-wide genotyping array 2021-03-23 32752121 Nedoszytko B 2020-07-31 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/32752121 Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups. Systemic mastocytosis 93 European ancestry cases, 5,606 European ancestry controls NA Illumina [281811] 17 systemic mastocytosis http://purl.obolibrary.org/obo/MONDO_0016586 GCST011382 Genome-wide genotyping array 2021-03-23 32752121 Nedoszytko B 2020-07-31 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/32752121 Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups. Cutaneous mastocytosis 141 European ancestry cases, 5,606 European ancestry controls NA Illumina [281811] 10 cutaneous mastocytosis http://www.ebi.ac.uk/efo/EFO_1000886 GCST011381 Genome-wide genotyping array 2021-03-23 32752121 Nedoszytko B 2020-07-31 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/32752121 Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups. Cutaneous mastocytosis (adult) 65 European ancestry cases, 5,606 European ancestry controls NA Illumina [281811] 4 cutaneous mastocytosis http://www.ebi.ac.uk/efo/EFO_1000886 GCST011380 Genome-wide genotyping array 2021-03-23 32752121 Nedoszytko B 2020-07-31 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/32752121 Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups. Mastocytosis 234 European ancestry cases, 5,606 European ancestry controls NA Illumina [281811] 20 Mastocytosis http://www.ebi.ac.uk/efo/EFO_0009001 GCST011383 Genome-wide genotyping array 2021-03-23 32752121 Nedoszytko B 2020-07-31 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/32752121 Results from a Genome-Wide Association Study (GWAS) in Mastocytosis Reveal New Gene Polymorphisms Associated with WHO Subgroups. Cutaneous mastocytosis (childhood) 78 European ancestry cases, 5,606 European ancestry controls NA Illumina [281811] 11 cutaneous mastocytosis http://www.ebi.ac.uk/efo/EFO_1000886 GCST011379 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 2-hydroxyisobutyrate levels 996 European ancestry individuals NA Illumina [283704] 0 2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010979 GCST90013539 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 3-aminoisobutyrate levels 996 European ancestry individuals NA Illumina [283704] 0 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90013540 Genome-wide genotyping array 2021-03-05 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 3-hydroxybutyrate + 3-aminoisobutyrate levels 996 European ancestry individuals NA Illumina [283704] 2 3-aminoisobutyrate measurement, 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980, http://www.ebi.ac.uk/efo/EFO_0010983 GCST90013541 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 3-hydroxyisobutyrate levels 996 European ancestry individuals NA Illumina [283704] 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90013542 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 3-hydroxyisovalerate levels 996 European ancestry individuals NA Illumina [283704] 0 3-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0010984 GCST90013543 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 3-Indoxylsulfate levels 996 European ancestry individuals NA Illumina [283704] 0 3-Indoxylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0010985 GCST90013544 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 4-deoxyerythronic acid levels 996 European ancestry individuals NA Illumina [283704] 0 4-deoxyerythronic acid measurement http://www.ebi.ac.uk/efo/EFO_0010986 GCST90013545 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 4-deoxythreonic acid levels 996 European ancestry individuals NA Illumina [283704] 0 4-deoxythreonic acid measurement http://www.ebi.ac.uk/efo/EFO_0010987 GCST90013546 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. 5-oxoproline levels 996 European ancestry individuals NA Illumina [283704] 0 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90013547 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Acetate levels 996 European ancestry individuals NA Illumina [283704] 0 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90013548 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Acetone levels 996 European ancestry individuals NA Illumina [283704] 0 acetone measurement http://www.ebi.ac.uk/efo/EFO_0010989 GCST90013549 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Alanine levels 996 European ancestry individuals NA Illumina [283704] 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90013550 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Carnitine levels 996 European ancestry individuals NA Illumina [283704] 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90013551 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Citrate levels 996 European ancestry individuals NA Illumina [283704] 0 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90013552 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Creatine levels 996 European ancestry individuals NA Illumina [283704] 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90013553 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Creatinine levels 996 European ancestry individuals NA Illumina [283704] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90013554 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Dimethylamine levels 996 European ancestry individuals NA Illumina [283704] 0 dimethylamine measurement http://www.ebi.ac.uk/efo/EFO_0010990 GCST90013555 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Formate levels 996 European ancestry individuals NA Illumina [283704] 0 formate measurement http://www.ebi.ac.uk/efo/EFO_0010991 GCST90013556 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Glucose levels 996 European ancestry individuals NA Illumina [283704] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90013557 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Glutamine levels 996 European ancestry individuals NA Illumina [283704] 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90013558 Genome-wide genotyping array 2021-03-05 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Glycine levels 996 European ancestry individuals NA Illumina [283704] 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90013559 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Hippurate levels 996 European ancestry individuals NA Illumina [283704] 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90013560 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Isoleucine levels 996 European ancestry individuals NA Illumina [283704] 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90013561 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Lactate levels 996 European ancestry individuals NA Illumina [283704] 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90013562 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Leucine levels 996 European ancestry individuals NA Illumina [283704] 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90013563 Genome-wide genotyping array 2021-03-05 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Lysine levels 996 European ancestry individuals NA Illumina [283704] 1 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90013564 Genome-wide genotyping array 2021-03-05 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. N-acetyl neuraminic acid levels 996 European ancestry individuals NA Illumina [283704] 2 n-acetyl neuraminic acid measurement http://www.ebi.ac.uk/efo/EFO_0010993 GCST90013565 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. N-methyl-2-pyridone-5-carboxamide levels 996 European ancestry individuals NA Illumina [283704] 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90013566 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. N-methylnicotinic acid levels 996 European ancestry individuals NA Illumina [283704] 0 n-methylnicotinic acid measurement http://www.ebi.ac.uk/efo/EFO_0010995 GCST90013567 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. N-methylpicolinic acid levels 996 European ancestry individuals NA Illumina [283704] 0 n-methylpicolinic acid measurement http://www.ebi.ac.uk/efo/EFO_0010996 GCST90013568 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. N1-methyl-nicotinamide levels 996 European ancestry individuals NA Illumina [283704] 0 n1-methyl-nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0010997 GCST90013569 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. P-cresol sulfate levels 996 European ancestry individuals NA Illumina [283704] 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90013570 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. P-hydroxyphenylacetate levels 996 European ancestry individuals NA Illumina [283704] 0 p-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0010999 GCST90013571 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Pantothenic acid levels 996 European ancestry individuals NA Illumina [283704] 0 pantothenic acid mesurement http://www.ebi.ac.uk/efo/EFO_0010519 GCST90013572 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Proline betaine levels 996 European ancestry individuals NA Illumina [283704] 0 proline betaine measurement http://www.ebi.ac.uk/efo/EFO_0011000 GCST90013573 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Scyllo-inositol levels 996 European ancestry individuals NA Illumina [283704] 0 scyllo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0011001 GCST90013574 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Succinate levels 996 European ancestry individuals NA Illumina [283704] 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90013575 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Sucrose levels 996 European ancestry individuals NA Illumina [283704] 0 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90013576 Genome-wide genotyping array 2021-03-05 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Taurine levels 996 European ancestry individuals NA Illumina [283704] 1 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90013577 Genome-wide genotyping array 2021-03-05 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Trimethylamine levels 996 European ancestry individuals NA Illumina [283704] 1 trimethylamine measurement http://www.ebi.ac.uk/efo/EFO_0011003 GCST90013578 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Trimethylamine oxide levels 996 European ancestry individuals NA Illumina [283704] 0 trimethylamine oxide measurement http://www.ebi.ac.uk/efo/EFO_0011004 GCST90013579 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Tyrosine levels 996 European ancestry individuals NA Illumina [283704] 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90013580 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Urea levels 996 European ancestry individuals NA Illumina [283704] 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90013581 Genome-wide genotyping array 2021-02-17 33283231 Calvo-Serra B 2020-12-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33283231 Urinary metabolite quantitative trait loci in children and their interaction with dietary factors. Valine levels 996 European ancestry individuals NA Illumina [283704] 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90013582 Genome-wide genotyping array 2021-07-27 33382417 Batai K 2020-12-31 J Nutr www.ncbi.nlm.nih.gov/pubmed/33382417 Genome-Wide Association Study of Response to Selenium Supplementation and Circulating Selenium Concentrations in Adults of European Descent. Plasma selenium concentration 1,211 European ancestry individuals NA Illumina [7663546] (imputed) 3 selenium measurement http://www.ebi.ac.uk/efo/EFO_0006331 GCST012070 Genome-wide genotyping array 2021-07-27 33382417 Batai K 2020-12-31 J Nutr www.ncbi.nlm.nih.gov/pubmed/33382417 Genome-Wide Association Study of Response to Selenium Supplementation and Circulating Selenium Concentrations in Adults of European Descent. Response to selenium supplementation (change in plasma selenium concentration) 428 European ancestry individuals NA Illumina [7663546] (imputed) 14 selenium measurement, response to dietary selenium supplementation http://www.ebi.ac.uk/efo/EFO_0006331, http://www.ebi.ac.uk/efo/EFO_0600021 GCST012071 Genome-wide genotyping array 2020-08-26 25998175 Larson NB 2015-05-22 Ann Hum Genet www.ncbi.nlm.nih.gov/pubmed/25998175 Trans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA). Hepatocyte growth factor levels 1,550 African American individuals, 762 Chinese ancestry individuals, 2,477 European ancestry individuals, 1,412 Hispanic individuals NA Illumina [377173] 7 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST010461 Targeted genotyping array [Exome array, Cardio-Metabochip] 2020-10-08 32790701 Rode M 2020-08-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/32790701 Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure. Arterial stiffness (carotid-femoral pulse wave velocity) 6,430 European ancestry individuals NA Affymetrix [11342744] (imputed) 2 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST010655 Genome-wide genotyping array 2020-10-08 32790701 Rode M 2020-08-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/32790701 Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure. Arterial stiffness (brachial-femoral pulse wave velocity) 3,643 European ancestry individuals NA Affymetrix [11342744] (imputed) 5 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST010654 Genome-wide genotyping array 2020-10-08 32790701 Rode M 2020-08-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/32790701 Genome-wide association analysis of pulse wave velocity traits provide new insights into the causal relationship between arterial stiffness and blood pressure. Arterial stiffness (brachial-ankle pulse wave velocity) 6,734 European ancestry individuals NA Affymetrix [11342744] (imputed) 3 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST010656 Genome-wide genotyping array 2021-03-30 32808324 Hu J 2020-08-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32808324 Supervariants identification for breast cancer. Breast cancer 5,653 cases, 28,241 controls NA NR [41502298] (imputed) 8 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST011433 Genome-wide genotyping array 2022-10-04 32378051 O'Donnell PH 2020-05-06 Breast Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/32378051 Clinical evaluation of germline polymorphisms associated with capecitabine toxicity in breast cancer: TBCRC-015. Capecitabine toxicity in breast cancer 147 European ancestry individuals NA Illumina [730525] 0 response to CAPOX-B http://www.ebi.ac.uk/efo/EFO_0007683 GCST012997 Genome-wide genotyping array 2021-03-24 32723749 Kwon YC 2020-07-28 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32723749 Genome-wide association study in a Korean population identifies six novel susceptibility loci for rheumatoid arthritis. Rheumatoid arthritis 4,068 Korean ancestry cases, 36,487 Korean ancestry controls NA Illumina [NR] (imputed) 19 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST011389 Genome-wide genotyping array 2021-03-24 32719433 Liu Y 2020-07-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/32719433 Four pleiotropic loci associated with fat mass and lean mass. Leg fat mass (lean adjusted) 9,684 European ancestry individuals, 1,541 Han Chinese ancestry individuals, 847 African American individuals, 445 Hispanic individuals 370,097 European ancestry individuals Affymetrix, Illumina [6879267] (imputed) 3 lean mass-adjusted fat body mass http://www.ebi.ac.uk/efo/EFO_0009890 GCST011393 Genome-wide genotyping array 2021-03-24 32719433 Liu Y 2020-07-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/32719433 Four pleiotropic loci associated with fat mass and lean mass. Leg lean mass (fat adjusted) 9,684 European ancestry individuals, 1,541 Han Chinese ancestry individuals, 847 African American individuals, 445 Hispanic individuals 370,097 European ancestry individuals Affymetrix, Illumina [6879267] (imputed) 2 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST011392 Genome-wide genotyping array 2021-03-24 32719433 Liu Y 2020-07-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/32719433 Four pleiotropic loci associated with fat mass and lean mass. Leg fat mass and leg lean mass (pleiotropy) 9,684 European ancestry individuals, 1,541 Han Chinese ancestry individuals, 847 African American individuals, 445 Hispanic individuals 370,097 European ancestry individuals Affymetrix, Illumina [6879267] (imputed) 4 fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST011394 Genome-wide genotyping array 2021-03-28 32757270 Ruiz-Pinto S 2020-08-05 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32757270 Regulatory CDH4 genetic variants associate with risk to develop capecitabine-induced hand-foot syndrome. Capecitabine-induced hand-foot syndrome in breast or colorectal cancer 88 cases, 78 controls 24 cases, 61 controls Illumina [520052] 4 Hand-foot syndrome, response to fluoropyrimidines http://www.ebi.ac.uk/efo/EFO_1001893, http://www.ebi.ac.uk/efo/EFO_0010825 GCST011420 Genome-wide genotyping array 2021-07-02 32998551 Docherty AR 2020-10-01 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/32998551 Genome-Wide Association Study of Suicide Death and Polygenic Prediction of Clinical Antecedents. Suicide 3,413 European ancestry cases, 14,810 European ancestry controls NA Illumina [7519308] (imputed) 10 suicide http://www.ebi.ac.uk/efo/EFO_0007624 GCST011994 Genome-wide genotyping array 2021-03-30 32826979 Meguro A 2020-08-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32826979 Genetic control of CCL24, POR, and IL23R contributes to the pathogenesis of sarcoidosis. Sarcoidosis 685 Japanese ancestry cases, 847 Japanese ancestry controls 907 Japanese ancestry cases, 252 European ancestry cases, 1,042 Japanese ancestry controls, 256 European ancestry controls Illumina [530466] (imputed) 4 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST011437 Genome-wide genotyping array 2020-10-08 32912094 Jaworek T 2020-09-11 Stroke www.ncbi.nlm.nih.gov/pubmed/32912094 Exome Array Analysis of Early-Onset Ischemic Stroke. Early-onset ischemic stroke 330 African American cases, 393 European ancestry cases, 298 African American controls, 428 European ancestry controls NA Illumina [243497] 3 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST010652 Exome genotyping array [Exome array] 2020-12-09 32298765 Anstee QM 2020-04-13 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32298765 Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. Hepatic steatosis in non-alcoholic fatty liver disease 1,469 European ancestry individuals 504 European ancestry individuals Illumina [7412561] (imputed) 0 Hepatic steatosis http://purl.obolibrary.org/obo/HP_0001397 GCST010858 Genome-wide genotyping array 2020-12-10 32298765 Anstee QM 2020-04-13 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32298765 Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. Liver fibrosis in non-alcoholic fatty liver disease 1,481 European ancestry individuals 557 European ancestry individuals Illumina [7412560] (imputed) 0 liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0010576 GCST010864 Genome-wide genotyping array 2020-12-10 32298765 Anstee QM 2020-04-13 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32298765 Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. Non-alcoholic steatohepatitis activity score in non-alcoholic fatty liver disease 1,467 European ancestry individuals 501 European ancestry individuals Illumina [7412560] (imputed) 0 non-alcoholic fatty liver disease severity measurement http://www.ebi.ac.uk/efo/EFO_0008421 GCST010863 Genome-wide genotyping array 2020-12-10 32298765 Anstee QM 2020-04-13 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32298765 Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. Non-alcoholic fatty liver disease activity score in non-alcoholic fatty liver disease 1,467 European ancestry individuals 501 European ancestry individuals Illumina [7412560] (imputed) 0 non-alcoholic fatty liver disease severity measurement http://www.ebi.ac.uk/efo/EFO_0008421 GCST010862 Genome-wide genotyping array 2020-12-10 32298765 Anstee QM 2020-04-13 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32298765 Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. Nonalcoholic steatohepatitis 836 European ancestry cases, 17,781 European ancestry controls NA Illumina [7412560] (imputed) 8 non-alcoholic steatohepatitis http://www.ebi.ac.uk/efo/EFO_1001249 GCST010861 Genome-wide genotyping array 2020-12-10 32298765 Anstee QM 2020-04-13 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32298765 Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. Severe liver fibrosis and non-alcoholic fatty liver disease 386 European ancestry cases, 17,781 European ancestry controls 134 European ancestry cases, 945 European ancestry controls Illumina [7412560] (imputed) 0 non-alcoholic fatty liver disease, Hepatic fibrosis, liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0003095, http://purl.obolibrary.org/obo/HP_0001395, http://www.ebi.ac.uk/efo/EFO_0010576 GCST010860 Genome-wide genotyping array 2020-12-09 32298765 Anstee QM 2020-04-13 J Hepatol www.ncbi.nlm.nih.gov/pubmed/32298765 Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. Nonalcoholic fatty liver disease 1,483 European ancestry cases, 17,781 European ancestry controls 559 European ancestry cases, 945 European ancestry controls Illumina [7412560] (imputed) 2 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90011885 Genome-wide genotyping array 2021-05-10 32998964 Trendowski MR 2020-09-30 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/32998964 Clinical and Genome-Wide Analysis of Multiple Severe Cisplatin-Induced Neurotoxicities in Adult-Onset Cancer Survivors. Multiple severe cisplatin-induced neurotixicitiies in testicular cancer survivors 104 European ancestry cases, 196 European ancestry controls NA Illumina [5385324] (imputed) 5 response to cisplatin http://purl.obolibrary.org/obo/GO_0072718 GCST011637 Genome-wide genotyping array 2021-05-26 32928300 Sugino S 2020-09-14 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/32928300 Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study. Postoperative nausea and vomiting 12 Japanese ancestry cases, 12 Japanese ancestry controls 46 Japanese ancestry cases, 186 Japanese ancestry controls NR [6714496] (imputed) 0 post operative nausea and vomiting http://www.ebi.ac.uk/efo/EFO_0004888 GCST011738 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume x hypertension interaction (2df) 46,055 European ancestry individuals NA Affymetrix, Illumina [9900000] (imputed) 26 hypertension, white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0005665 GCST011953 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume x hypertension interaction (2df) 46,055 European ancestry individuals, 2,469 African American individuals NA Affymetrix, Illumina [9900000] (imputed) 26 hypertension, white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0005665 GCST011952 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume (adjusted for hypertension) 2,469 African American individuals NA Affymetrix, Illumina [9900000] (imputed) 1 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST011951 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume (adjusted for hypertension) 46,055 European ancestry individuals NA Affymetrix, Illumina [9900000] (imputed) 43 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST011950 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume (adjusted for hypertension) 46,055 European ancestry individuals, 2,469 African American individuals NA Affymetrix, Illumina [9900000] (imputed) 46 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST011949 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume 2,516 African American individuals NA Affymetrix, Illumina [9900000] (imputed) 1 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST011948 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume 48,454 European ancestry individuals NA Affymetrix, Illumina [9900000] (imputed) 60 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST011947 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume 2,516 African American individuals, 48,454 European ancestry individuals NA Affymetrix, Illumina [9900000] (imputed) 47 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST011946 Genome-wide genotyping array 2021-06-22 33293549 Sargurupremraj M 2020-12-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33293549 Cerebral small vessel disease genomics and its implications across the lifespan. White matter hyperintensity volume x hypertension interaction (2df) 2,469 African American individuals NA Affymetrix, Illumina [9900000] (imputed) 5 hypertension, white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0005665 GCST011954 Genome-wide genotyping array 2021-03-30 33445220 Li Y 2021-01-14 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/33445220 Donor genetic variants as risk factors for thrombosis after liver transplantation: A genome-wide association study. Thrombosis in response to liver transplant 42 European ancestry pediatric cases, 268 European ancestry pediatric controls 64 European ancestry adult cases, 711 European ancestry adult controls Illumina [5393447] (imputed) 11 coronary thrombosis, GM11992 http://www.ebi.ac.uk/efo/EFO_1000883, http://www.ebi.ac.uk/efo/EFO_0001124 GCST011434 Genome-wide genotyping array 2021-02-18 33287642 Said MA 2020-12-08 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/33287642 Associations of Observational and Genetically Determined Caffeine Intake With Coronary Artery Disease and Diabetes Mellitus. Caffeine consumption from coffee 373,522 European ancestry individuals NA Affymetrix [19400838] (imputed) 24 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST011125 Genome-wide genotyping array 2021-02-18 33287642 Said MA 2020-12-08 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/33287642 Associations of Observational and Genetically Determined Caffeine Intake With Coronary Artery Disease and Diabetes Mellitus. Caffeine consumption from tea 395,866 European ancestry individuals NA Affymetrix [19400838] (imputed) 24 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST011124 Genome-wide genotyping array 2021-02-18 33287642 Said MA 2020-12-08 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/33287642 Associations of Observational and Genetically Determined Caffeine Intake With Coronary Artery Disease and Diabetes Mellitus. Caffeine consumption from coffee or tea 362,316 European ancestry individuals NA Affymetrix [19400838] (imputed) 37 coffee consumption measurement, tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781, http://www.ebi.ac.uk/efo/EFO_0010091 GCST011126 Genome-wide genotyping array 2021-07-01 33381925 Buchanan VL 2020-12-30 Pediatr Obes www.ncbi.nlm.nih.gov/pubmed/33381925 Genome-wide association study identifying novel variant for fasting insulin and allelic heterogeneity in known glycemic loci in Chilean adolescents: The Santiago Longitudinal Study. Fasting insulin 543 Chilean individuals 18,637 European ancestry individuals, 14,270 Hispanic individuals, 7,683 African ancestry individuals, 1,900 Asian ancestry individuals, 1,398 Native Hawaiian ancestry individuals, 392 individuals Illumina [NR] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST011982 Genome-wide genotyping array 2021-07-01 33381925 Buchanan VL 2020-12-30 Pediatr Obes www.ncbi.nlm.nih.gov/pubmed/33381925 Genome-wide association study identifying novel variant for fasting insulin and allelic heterogeneity in known glycemic loci in Chilean adolescents: The Santiago Longitudinal Study. Homeostasis model assessment of insulin resistance 543 Chilean individuals NA Illumina [NR] (imputed) 15 HOMA-IR http://www.ebi.ac.uk/efo/EFO_0004501 GCST011981 Genome-wide genotyping array 2021-07-01 33381925 Buchanan VL 2020-12-30 Pediatr Obes www.ncbi.nlm.nih.gov/pubmed/33381925 Genome-wide association study identifying novel variant for fasting insulin and allelic heterogeneity in known glycemic loci in Chilean adolescents: The Santiago Longitudinal Study. Fasting glucose 543 Chilean individuals NA Illumina [NR] (imputed) 24 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST011983 Genome-wide genotyping array 2021-07-09 33428804 Chalmer MA 2021-01-11 Eur J Neurol www.ncbi.nlm.nih.gov/pubmed/33428804 Chronic migraine: Genetics or environment? Migraine (chronic vs episodic) 127 Danish ancestry chronic migraine cases, 926 Danish ancestry episodic migraine cases NA Illumina [6101288] (imputed) 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST012023 Genome-wide genotyping array 2021-07-09 33428804 Chalmer MA 2021-01-11 Eur J Neurol www.ncbi.nlm.nih.gov/pubmed/33428804 Chronic migraine: Genetics or environment? Migraine (proposed chronic vs episodic) 268 Danish ancestry proposed chronic migraine cases, 785 Danish ancestry episodic migraine cases NA Illumina [6101288] (imputed) 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST012022 Genome-wide genotyping array 2021-02-17 33370439 Dusingize JC 2020-12-28 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33370439 Genetically determined risk of keratinocyte carcinoma and risk of other cancers. Keratinocyte cancer (MTAG) 669,243 European ancestry individuals NA NR [NR] 0 keratinocyte carcinoma http://www.ebi.ac.uk/efo/EFO_0010176 GCST011120 Genome-wide genotyping array 2021-02-17 33370439 Dusingize JC 2020-12-28 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33370439 Genetically determined risk of keratinocyte carcinoma and risk of other cancers. Keratinocyte cancer (MTAG) 323,345 European ancestry individuals NA NR [NR] 0 keratinocyte carcinoma http://www.ebi.ac.uk/efo/EFO_0010176 GCST011121 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Lymphocyte count 524,923 European ancestry individuals NA Affymetrix, Illumina [50265552] (imputed) 465 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90002316 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Lymphocyte count 89,266 East Asian ancestry individuals NA Affymetrix, Illumina [16289068] (imputed) 16 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90002317 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Lymphocyte count 7,541 Hispanic or Latin American individuals NA Affymetrix, Illumina [25652707] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90002318 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Lymphocyte count 8,163 South Asian ancestry individuals NA Affymetrix, Illumina [28469925] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90002319 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Lymphocyte count 643,370 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [23472807] (imputed) 409 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90002320 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin 11,974 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36043646] (imputed) 7 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002321 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin 486,823 European ancestry individuals NA Affymetrix, Illumina [50266654] (imputed) 423 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002322 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin 119,629 East Asian ancestry individuals NA Affymetrix, Illumina [16286228] (imputed) 77 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002323 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin 3,518 Hispanic or Latin American individuals NA Affymetrix, Illumina [24999652] (imputed) 1 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002324 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin 8,181 South Asian ancestry individuals NA Affymetrix, Illumina [28486451] (imputed) 10 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002325 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin 630,125 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [20825802] (imputed) 384 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002326 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin concentration 12,766 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36221496] (imputed) 2 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002327 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin concentration 491,553 European ancestry individuals NA Affymetrix, Illumina [50282193] (imputed) 191 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002328 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin concentration 126,151 East Asian ancestry individuals NA Affymetrix, Illumina [16289083] (imputed) 36 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002329 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin concentration 3,518 Hispanic or Latin American individuals NA Affymetrix, Illumina [24999636] (imputed) 1 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002330 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin concentration 8,185 South Asian ancestry individuals NA Affymetrix, Illumina [28487724] (imputed) 2 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002331 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular hemoglobin concentration 642,173 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [21126107] (imputed) 166 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90002332 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular volume 14,222 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36679766] (imputed) 2 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90002333 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular volume 544,127 European ancestry individuals NA Affymetrix, Illumina [50615308] (imputed) 466 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90002334 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular volume 121,047 East Asian ancestry individuals NA Affymetrix, Illumina [16286195] (imputed) 79 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90002335 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular volume 9,298 Hispanic or Latin American individuals NA Affymetrix, Illumina [26810224] (imputed) 6 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90002336 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular volume 8,188 South Asian ancestry individuals NA Affymetrix, Illumina [28492174] (imputed) 10 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90002337 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Mean corpuscular volume 696,882 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [24246363] (imputed) 454 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90002338 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Monocyte count 13,471 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36452625] (imputed) 10 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90002339 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Monocyte count 521,594 European ancestry individuals NA Affymetrix, Illumina [50262088] (imputed) 455 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90002340 Genome-wide genotyping array 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 56,802 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American individuals Illumina [232255] 8 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007307 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 23,861 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American men Illumina [220735] 3 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007308 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 32,940 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American women Illumina [227495] 6 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007309 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 49,909 European ancestry individuals Illumina [204641] 7 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007310 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 21,921 European ancestry men Illumina [185219] 2 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007311 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 27,987 European ancestry women Illumina [193201] 5 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007312 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 56,802 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American individuals Illumina [92082] 5 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007313 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 23,861 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American men Illumina [60771] 2 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007314 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 32,940 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American women Illumina [86076] 3 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007315 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 49,909 European ancestry individuals Illumina [54083] 4 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007316 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 21,921 European ancestry men Illumina [46904] 1 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007317 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels 27,987 European ancestry women Illumina [49551] 2 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90007318 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 56,708 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American individuals Illumina [232237] 8 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007319 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 23,822 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American men Illumina [220721] 7 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007320 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 32,886 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American women Illumina [227473] 8 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007321 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 49,830 European ancestry individuals Illumina [204609] 7 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007322 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 21,883 European ancestry men Illumina [185190] 5 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007323 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 27,947 European ancestry women Illumina [193169] 7 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007324 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 56,708 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American individuals Illumina [92057] 6 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007325 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 23,822 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American men Illumina [60745] 2 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007326 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 32,886 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American women Illumina [86054] 6 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007327 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 49,830 European ancestry individuals Illumina [54056] 5 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007328 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 21,883 European ancestry men Illumina [46877] 2 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007329 Exome genotyping array [Illumina HumanExome BeadChip] 2020-10-02 32917775 Yaghootkar H 2020-09-11 Diabetes www.ncbi.nlm.nih.gov/pubmed/32917775 Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity. circulating leptin levels adjusted for BMI 27,947 European ancestry women Illumina [49530] 6 BMI-adjusted leptin measurement http://www.ebi.ac.uk/efo/EFO_0007793 GCST90007330 Exome genotyping array [Illumina HumanExome BeadChip] 2020-09-04 32472697 Verma SS 2020-05-30 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32472697 Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC). Cardiovascular death or myocardial infarction in response to clopidogrel treatment 102 European ancestry cases, 2,068 European ancestry controls NA Illumina [5009928] (imputed) 9 response to clopidogrel, cardiovascular event measurement http://purl.obolibrary.org/obo/GO_1903493, http://www.ebi.ac.uk/efo/EFO_0006919 GCST010482 Genome-wide genotyping array 2020-09-04 32472697 Verma SS 2020-05-30 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32472697 Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC). Cardiovascular death, myocardial infarction or stroke in response to clopidogrel treatment 72 European ancestry cases, 1,375 European ancestry controls NA Illumina [5009928] (imputed) 6 stroke, response to clopidogrel, cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0000712, http://purl.obolibrary.org/obo/GO_1903493, http://www.ebi.ac.uk/efo/EFO_0006919 GCST010483 Genome-wide genotyping array 2020-09-04 32472697 Verma SS 2020-05-30 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32472697 Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC). Stent thrombosis in response to clopidogrel treatment 37 European ancestry cases, 2,542 European ancestry controls NA Illumina [5009928] (imputed) 6 response to clopidogrel, cardiovascular event measurement http://purl.obolibrary.org/obo/GO_1903493, http://www.ebi.ac.uk/efo/EFO_0006919 GCST010484 Genome-wide genotyping array 2020-09-04 32472697 Verma SS 2020-05-30 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32472697 Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC). Platelet reactivity in response to clopidogrel treatment 2,592 European ancestry individuals NA Illumina [5009928] (imputed) 20 platelet reactivity measurement, response to clopidogrel http://www.ebi.ac.uk/efo/EFO_0004985, http://purl.obolibrary.org/obo/GO_1903493 GCST010485 Genome-wide genotyping array 2021-02-02 33111402 Tan MMX 2020-10-28 Mov Disord www.ncbi.nlm.nih.gov/pubmed/33111402 Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease. Parkinson's disease progression (motor) 2,848 individuals NA Illumina [5918868] (imputed) 10 Parkinson disease, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0005180, http://www.ebi.ac.uk/efo/EFO_0008336 GCST011038 Genome-wide genotyping array, Genome-wide sequencing 2021-02-02 33111402 Tan MMX 2020-10-28 Mov Disord www.ncbi.nlm.nih.gov/pubmed/33111402 Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease. Parkinson's disease progression (cognitive) 2,788 individuals NA Illumina [5918868] (imputed) 10 Parkinson disease, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0005180, http://www.ebi.ac.uk/efo/EFO_0008336 GCST011037 Genome-wide genotyping array, Genome-wide sequencing 2021-02-02 33111402 Tan MMX 2020-10-28 Mov Disord www.ncbi.nlm.nih.gov/pubmed/33111402 Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease. Parkinson's disease progression (composite) 2,755 individuals NA Illumina [5918868] (imputed) 10 Parkinson disease, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0005180, http://www.ebi.ac.uk/efo/EFO_0008336 GCST011039 Genome-wide genotyping array, Genome-wide sequencing 2020-08-26 32671202 Du M 2020-05-20 Sci Adv www.ncbi.nlm.nih.gov/pubmed/32671202 Remote modulation of lncRNA GCLET by risk variant at 16p13 underlying genetic susceptibility to gastric cancer. Gastric cancer 1,625 Chinese ancestry cases, 2,100 Chinese ancestry controls 5,353 Chinese ancestry cases, 6,685 Chinese ancestry controls, 254 European ancestry cases, 2,835 European ancestry controls NR [4817140] (imputed) 2 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST010462 Genome-wide genotyping array 2021-03-24 32724131 Li QS 2020-07-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32724131 Genome-wide association study and polygenic risk score analysis of esketamine treatment response. Response to esketamine in treatment resistant depression 255 European ancestry individuals NA NR [NR] (imputed) 40 response to ketamine http://www.ebi.ac.uk/efo/EFO_0009748 GCST011398 Genome-wide genotyping array 2021-03-24 32724131 Li QS 2020-07-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32724131 Genome-wide association study and polygenic risk score analysis of esketamine treatment response. Response to esketamine (responder status) in treatment resistant depression 255 European ancestry individuals NA NR [NR] (imputed) 11 response to ketamine http://www.ebi.ac.uk/efo/EFO_0009748 GCST011397 Genome-wide genotyping array 2021-03-24 32724131 Li QS 2020-07-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32724131 Genome-wide association study and polygenic risk score analysis of esketamine treatment response. Response to esketamine (remission) in treatment resistant depression 255 European ancestry remitters, 272 European ancestry non-remitters NA NR [NR] (imputed) 5 response to ketamine http://www.ebi.ac.uk/efo/EFO_0009748 GCST011396 Genome-wide genotyping array 2021-02-03 32619740 Makarawate P 2020-06-30 Heart Rhythm www.ncbi.nlm.nih.gov/pubmed/32619740 Common and rare susceptibility genetic variants predisposing to Brugada Syndrome in Thailand. Brugada syndrome 154 Thai cases, 432 Thai controls NA Illumina [5310833] (imputed) 3 Brugada syndrome http://purl.obolibrary.org/obo/MONDO_0015263 GCST011054 Genome-wide genotyping array 2020-09-12 32762793 Jang SK 2020-08-07 Psychol Med www.ncbi.nlm.nih.gov/pubmed/32762793 Genetic correlation, pleiotropy, and causal associations between substance use and psychiatric disorder. Substance uses or psychiatric disorders (pleiotropy) Up to 1,232,09 European ancestry individuals with substance use, 53,293 European ancestry ADHD cases, 72,517 European ancestry anorexia cases, 51,710 European ancestry bipolar disorder cases, 173,005 European ancestry major depressive disorder cases, 105,318 European ancestry schizophrenia cases, 1,475,951 European ancestry controls NA NR [NR] 0 major depressive episode, bipolar disorder, schizophrenia, substance abuse, anorexia nervosa, ADHD symptom measurement http://www.ebi.ac.uk/efo/EFO_0007634, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0002491, http://purl.obolibrary.org/obo/MONDO_0005351, http://www.ebi.ac.uk/efo/EFO_0007860 GCST010542 Genome-wide genotyping array 2021-02-16 32671597 Streicher SA 2020-07-15 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32671597 A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish population. Pancreatic cancer 604 Jewish cases, 2,332 Jewish controls NA Affymetrix, Illumina [1286673] (imputed) 2 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST011117 Genome-wide genotyping array 2021-05-14 32719713 Zhang F 2020-07-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/32719713 Independent Replication on Genome-Wide Association Study Signals Identifies IRF3 as a Novel Locus for Systemic Lupus Erythematosus. Systemic lupus erythematosus 4,943 European ancestry cases, 2,485 Asian ancestry cases, 8,483 European ancestry controls, 3,947 Asian ancestry controls 2,269 Han Chinese ancestry cases, 5,073 Han Chinese ancestry controls NR [NR] (imputed) 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST011661 Genome-wide genotyping array 2021-02-23 32709000 Jeong H 2020-07-17 Nutrients www.ncbi.nlm.nih.gov/pubmed/32709000 Identifying Interactions between Dietary Sodium, Potassium, Sodium-Potassium Ratios, and FGF5 rs16998073 Variants and Their Associated Risk for Hypertension in Korean Adults. Hypertension 8,178 Korean ancestry cases, 9,558 Korean ancestry controls NA Affymetrix [NR] 23 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST011141 Genome-wide genotyping array 2020-09-21 32516399 Lin C 2020-06-09 Chem Senses www.ncbi.nlm.nih.gov/pubmed/32516399 Studies of human twins reveal genetic variation that affects dietary fat perception. Dietary fat liking 331 European ancestry individuals, 50 African ancestry individuals, 19 individuals NA Illumina [4234798] (imputed) 10 dietary fat liking measurement http://www.ebi.ac.uk/efo/EFO_0010816 GCST010600 Genome-wide genotyping array 2020-09-21 32516399 Lin C 2020-06-09 Chem Senses www.ncbi.nlm.nih.gov/pubmed/32516399 Studies of human twins reveal genetic variation that affects dietary fat perception. Dietary fat liking 331 European ancestry individuals, 50 African ancestry individuals, 19 individuals NA Illumina [4234798] (imputed) 13 dietary fat liking measurement http://www.ebi.ac.uk/efo/EFO_0010816 GCST010599 Genome-wide genotyping array 2020-11-02 32517579 Armstrong NJ 2020-06-10 Stroke www.ncbi.nlm.nih.gov/pubmed/32517579 Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities. Deep white matter hyperintensities 16,832 European ancestry individuals, 736 African American individuals, 658 Hispanic individuals 8,428 European and unknown ancestry individuals Affymetrix, Illumina [NR] (imputed) 45 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST010727 Genome-wide genotyping array 2020-11-02 32517579 Armstrong NJ 2020-06-10 Stroke www.ncbi.nlm.nih.gov/pubmed/32517579 Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities. Periventricular white matter hyperintensities 16,832 European ancestry individuals, 736 African American individuals, 658 Hispanic individuals 8,428 European and unknown ancestry individuals Affymetrix, Illumina [NR] (imputed) 82 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST010726 Genome-wide genotyping array 2021-07-01 33037222 Sieh W 2020-10-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33037222 Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk. Mammographic density (dense area) 24,192 European ancestry individuals NA Affymetrix [9906178] (imputed) 19 mammographic density measurement http://www.ebi.ac.uk/efo/EFO_0005941 GCST90011731 Genome-wide genotyping array 2021-07-01 33037222 Sieh W 2020-10-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33037222 Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk. Mammographic density (non-dense area) 24,192 European ancestry individuals NA Affymetrix [9906178] (imputed) 15 mammographic density measurement http://www.ebi.ac.uk/efo/EFO_0005941 GCST90011732 Genome-wide genotyping array 2021-07-01 33037222 Sieh W 2020-10-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33037222 Identification of 31 loci for mammographic density phenotypes and their associations with breast cancer risk. Percent mammographic density 24,192 European ancestry individuals NA Affymetrix [9906178] (imputed) 22 mammographic density percentage http://www.ebi.ac.uk/efo/EFO_0006502 GCST90011733 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Bifidobacterium) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006987 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Bacteroides) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006988 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Parabacteroides) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006989 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Prevotella) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006990 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Streptococcus) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006991 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unclassified genus belonging to family Clostridiaceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006992 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unclassified genus belonging to the order Clostridiales) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006993 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Ruminococcus belonging to family Erysipelotrichaceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 12 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006994 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unclassified genus belonging to family Lachnospiraceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006995 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Blautia) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006996 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Coprococcus) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006997 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Dorea) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006998 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unassigned genus belonging to family Lachnospiraceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90006999 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unclassified genus belonging to family Ruminococcaceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007000 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Faecalibacterium) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007001 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Oscillospira) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007002 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Ruminococcus belonging to family Lachnospiraceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007003 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unassigned genus belonging to family Clostridiales) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007004 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Eubacterium belonging to family Erysipelotrichaceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007005 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unclassified genus belonging to family Erysipelotrichaceae) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007006 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Sutterella) 1,068 Japanese ancestry individuals NA Illumina [6380737] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007007 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Prevotella) 527 Japanese ancestry men NA Illumina [544877] 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007008 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Faecalibacterium) 527 Japanese ancestry men NA Illumina [544877] 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007009 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (Oscillospira) 541 Japanese ancestry women NA Illumina [545605] 7 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007010 Genome-wide genotyping array 2020-12-04 33208821 Ishida S 2020-11-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33208821 Genome-wide association studies and heritability analysis reveal the involvement of host genetics in the Japanese gut microbiota. Gut microbiota relative abundance (unclassified genus belonging to family Erysipelotrichaceae) 541 Japanese ancestry women NA Illumina [545605] 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90007011 Genome-wide genotyping array 2020-10-08 32429735 Lahrouchi N 2020-05-20 Circulation www.ncbi.nlm.nih.gov/pubmed/32429735 Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Long QT syndrome 1,238 European ancestry cases, 8,219 European ancestry controls, 418 Japanese cases, 1,617 Japanese controls NA Illumina [NR] (imputed) 5 familial long QT syndrome http://purl.obolibrary.org/obo/MONDO_0019171 GCST010651 Genome-wide genotyping array 2020-09-14 32556615 Liu Y 2020-06-18 Diabetologia www.ncbi.nlm.nih.gov/pubmed/32556615 Metabolomic and genetic associations with insulin resistance in pregnancy. Gestational insulin sensitivity 1,126 Afro-Caribbean individuals, 1,380 European ancestry individuals, 830 Mexican-American individuals, 1,192 Thai ancestry individuals NA Illumina [6168240] (imputed) 1 insulin sensitivity measurement http://www.ebi.ac.uk/efo/EFO_0004471 GCST010558 Genome-wide genotyping array 2020-11-04 32936915 Chai JF 2020-09-16 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/32936915 Genome-wide association for HbA1c in Malay identified deletion on SLC4A1 that influences HbA1c independent of glycemia. Glycated hemoglobin levels 1,721 Malay ancestry individuals NA Illumina [47095002] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90011771 Genome-wide genotyping array 2020-11-04 32936915 Chai JF 2020-09-16 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/32936915 Genome-wide association for HbA1c in Malay identified deletion on SLC4A1 that influences HbA1c independent of glycemia. Glycated hemoglobin levels 2,704 Malay ancestry individuals NA Illumina [47095002] (imputed) 4 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90011772 Genome-wide genotyping array, Exome-wide sequencing 2020-11-05 32554042 Jia X 2020-06-14 Kidney Int www.ncbi.nlm.nih.gov/pubmed/32554042 Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome. Childhood steroid-sensitive nephrotic syndrome 987 Japanese ancestry cases, 3,206 Japanese ancestry controls 249 Korean ancestry cases, 181 South Asian ancestry cases, 207 African ancestry cases, 307 European ancestry cases, 27 Hispanic cases, 85 Maghrebian ancestry cases, 3805 Korean ancestry controls, 8,255 South Asian ancestry controls, 5,657 African ancestry controls, 35,913 European ancestry controls, 5,789 Hispanic controls, 261 Moroccan ancestry controls Affymetrix [6834340] (imputed) 2 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST010731 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Basophil count 11,502 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [35912980] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90002291 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Basophil count 474,001 European ancestry individuals NA Affymetrix, Illumina [50036608] (imputed) 170 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90002292 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Basophil count 81,042 East Asian ancestry individuals NA Affymetrix, Illumina [16286709] (imputed) 25 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90002293 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Basophil count 2,969 Hispanic or Latin American individuals NA Affymetrix, Illumina [23758884] (imputed) 1 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90002294 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Basophil count 8,149 South Asian ancestry individuals NA Affymetrix, Illumina [28457669] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90002295 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Basophil count 577,663 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [19905671] (imputed) 150 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90002296 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Eosinophil counts 11,615 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [35935203] (imputed) 1 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90002297 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Eosinophil counts 474,237 European ancestry individuals NA Affymetrix, Illumina [50000174] (imputed) 376 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90002298 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Eosinophil counts 86,890 East Asian ancestry individuals NA Affymetrix, Illumina [16279099] (imputed) 31 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90002299 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Eosinophil counts 2,966 Hispanic or Latin American individuals NA Affymetrix, Illumina [23758042] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90002300 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Eosinophil counts 8,142 South Asian ancestry individuals NA Affymetrix, Illumina [28445528] (imputed) 1 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90002301 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Eosinophil counts 583,850 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [19872809] (imputed) 346 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90002302 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hematocrit 15,134 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36870619] (imputed) 1 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90002303 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hematocrit 562,259 European ancestry individuals NA Affymetrix, Illumina [50640577] (imputed) 392 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90002304 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hematocrit 142,940 East Asian ancestry individuals NA Affymetrix, Illumina [16289021] (imputed) 31 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90002305 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hematocrit 9,301 Hispanic or Latin American individuals NA Affymetrix, Illumina [26810352] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90002306 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hematocrit 8,189 South Asian ancestry individuals NA Affymetrix, Illumina [28493283] (imputed) 1 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90002307 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hematocrit 737,823 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [24558453] (imputed) 356 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90002308 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hemoglobin concentration 15,133 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36870618] (imputed) 2 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90002309 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hemoglobin concentration 563,946 European ancestry individuals NA Affymetrix, Illumina [50638016] (imputed) 402 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90002310 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hemoglobin concentration 149,861 East Asian ancestry individuals NA Affymetrix, Illumina [16709126] (imputed) 21 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90002311 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hemoglobin concentration 9,302 Hispanic or Latin American individuals NA Affymetrix, Illumina [26810352] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90002312 Genome-wide genotyping array 2020-09-16 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hemoglobin concentration 8,189 South Asian ancestry individuals NA Affymetrix, Illumina [28493177] (imputed) 2 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90002313 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Hemoglobin concentration 746,431 African American or Afro-Caribbean, African ancestry, European ancestry, East Asian ancestry, Hispanic or Latin American and South Asian ancestry individuals NA Affymetrix, Illumina [24653286] (imputed) 364 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90002314 Genome-wide genotyping array 2020-09-21 32888493 Chen MH 2020-09-01 Cell www.ncbi.nlm.nih.gov/pubmed/32888493 Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations. Lymphocyte count 13,477 African American or Afro-Caribbean and African ancestry individuals NA Affymetrix, Illumina [36456147] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90002315 Genome-wide genotyping array 2021-01-28 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. Electrocardiographic traits (multivariate) 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 64 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST011010 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. P wave duration 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 P wave duration http://www.ebi.ac.uk/efo/EFO_0005094 GCST011478 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. PR segment duration 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 PR segment http://www.ebi.ac.uk/efo/EFO_0005095 GCST011479 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. QRS duration 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST011480 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. ST segment duration 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 ST segment duration http://www.ebi.ac.uk/efo/EFO_0011033 GCST011481 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. T wave duration 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 T wave duration http://www.ebi.ac.uk/efo/EFO_0011034 GCST011482 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. TP segment duration 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 TP segment duration http://www.ebi.ac.uk/efo/EFO_0011035 GCST011483 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. PR interval 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST011484 Genome-wide genotyping array 2021-04-12 32602732 Baldassari AR 2020-06-30 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32602732 Multi-ethnic Genome-wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits. QT interval 17,873 European ancestry individuals, 12,749 Hispanic individuals, 5,408 African American individuals, 315 Chinese-American individuals NA Affymetrix, Illumina [22000000] (imputed) 0 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST011485 Genome-wide genotyping array 2021-07-09 33031748 Feofanova EV 2020-10-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33031748 A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos. Serum metabolite levels 3,926 Hispanic/Latino individuals 1,509 European ancestry individuals Illumina [13039987] (imputed) 119 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST012021 Genome-wide genotyping array 2021-07-09 33031748 Feofanova EV 2020-10-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33031748 A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos. Serum metabolite levels 3,926 Hispanic/Latino individuals NA Illumina [13039987] (imputed) 608 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST012020 Genome-wide genotyping array 2019-12-03 31375628 Tengvall K 2019-08-02 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/31375628 Molecular mimicry between Anoctamin 2 and Epstein-Barr virus nuclear antigen 1 associates with multiple sclerosis risk. Anti-anoctamin 2 antibody levels 11,936 European ancestry individuals NA Illumina [615763] 10 anti-anoctamin 2 antibody measurement http://www.ebi.ac.uk/efo/EFO_0010150 GCST009154 Genome-wide genotyping array 2020-07-22 32650023 Gabryszewski SJ 2020-07-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32650023 Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories. Allergic march (atopic dermatitis to allergic rhinitis) 225 African American child cases, 963 African American child controls 148 African American child cases, 1,151 African American child controls Illumina [52127467] (imputed) 1 atopic march http://www.ebi.ac.uk/efo/EFO_0007755 GCST90000019 Genome-wide genotyping array 2020-07-22 32650023 Gabryszewski SJ 2020-07-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32650023 Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories. Allergic march (atopic dermatitis to asthma) 335 African American child cases, 963 African American child controls 220 African American child cases, 1,151 African American child controls Illumina [52106158] (imputed) 1 atopic march http://www.ebi.ac.uk/efo/EFO_0007755 GCST90000020 Genome-wide genotyping array 2020-07-22 32650023 Gabryszewski SJ 2020-07-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32650023 Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories. Allergic march (atopic dermatitis to allergic rhinitis) 115 African American child male cases, 466 African American child male controls 74 African American child male cases, 543 African American child male controls Illumina [52184427] (imputed) 1 atopic march http://www.ebi.ac.uk/efo/EFO_0007755 GCST90000021 Genome-wide genotyping array 2020-07-22 32650023 Gabryszewski SJ 2020-07-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32650023 Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories. Allergic march (atopic dermatitis to asthma) 198 African American child male cases, 466 African American child male controls 127 African American child male cases, 543 African American child male controls Illumina [52169262] (imputed) 0 atopic march http://www.ebi.ac.uk/efo/EFO_0007755 GCST90000022 Genome-wide genotyping array 2020-07-22 32650023 Gabryszewski SJ 2020-07-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32650023 Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories. Allergic march (atopic dermatitis to allergic rhinitis) 110 African American child female cases, 496 African American child female controls 74 African American child female cases, 606 African American child female controls Illumina [52122499] (imputed) 1 atopic march http://www.ebi.ac.uk/efo/EFO_0007755 GCST90000023 Genome-wide genotyping array 2020-07-22 32650023 Gabryszewski SJ 2020-07-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32650023 Unsupervised Modeling and Genome-Wide Association Identify Novel Features of Allergic March Trajectories. Allergic march (atopic dermatitis to asthma) 137 African American child female cases, 496 African American child female controls 92 African American child female cases, 606 African American child female controls Illumina [52090676] (imputed) 0 atopic march http://www.ebi.ac.uk/efo/EFO_0007755 GCST90000024 Genome-wide genotyping array 2021-03-22 32756886 Nunez-Torres R 2020-08-05 JAMA Dermatol www.ncbi.nlm.nih.gov/pubmed/32756886 Association Between ABCB1 Genetic Variants and Persistent Chemotherapy-Induced Alopecia in Women With Breast Cancer. Persistent chemotherapy-induced alopecia in breast cancer 51 European ancestry cases, 122 European ancestry controls 20 European ancestry cases, 22 European ancestry controls Illumina [693898] 1 chemotherapy-induced alopecia, response to docetaxel trihydrate http://www.ebi.ac.uk/efo/EFO_0005400, http://purl.obolibrary.org/obo/GO_1902519 GCST011316 Genome-wide genotyping array 2020-08-13 32737300 Sallah N 2020-07-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32737300 Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections. Anti-Epstein-Barr virus nuclear antigen (EBNA) IgG levels 4,365 Ugandan ancestry individuals 2,162 European ancestry individuals Illumina [14929118] (imputed) 3 Epstein Barr virus nuclear antigen 1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0007790 GCST90000522 Genome-wide genotyping array 2020-08-13 32737300 Sallah N 2020-07-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32737300 Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections. Anti-Epstein-Barr virus viral capsid antigen (VCA) IgG levels 4,365 Ugandan ancestry individuals Illumina [14929118] (imputed) 0 Epstein Barr viral capsid antigen IgG measurement http://www.ebi.ac.uk/efo/EFO_0009274 GCST90000523 Genome-wide genotyping array 2020-08-13 32737300 Sallah N 2020-07-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32737300 Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections. Anti-Kaposi's sarcoma associated herpesvirus ORF73 IgG levels 4,365 Ugandan ancestry individuals Illumina [14929118] (imputed) 0 anti-Kaposi's sarcoma-associated herpesvirus antibody measurement http://www.ebi.ac.uk/efo/EFO_0010758 GCST90000524 Genome-wide genotyping array 2020-08-13 32737300 Sallah N 2020-07-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32737300 Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections. Anti-Kaposi's sarcoma associated herpesvirus K10.5 IgG levels 4,365 Ugandan ancestry individuals Illumina [14929118] (imputed) 0 anti-Kaposi's sarcoma-associated herpesvirus antibody measurement http://www.ebi.ac.uk/efo/EFO_0010758 GCST90000525 Genome-wide genotyping array 2020-08-13 32737300 Sallah N 2020-07-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32737300 Distinct genetic architectures and environmental factors associate with host response to the γ2-herpesvirus infections. Anti-Kaposi's sarcoma associated herpesvirus K8.1 IgG levels 4,365 Ugandan ancestry individuals Illumina [14929118] (imputed) 0 anti-Kaposi's sarcoma-associated herpesvirus antibody measurement http://www.ebi.ac.uk/efo/EFO_0010758 GCST90000526 Genome-wide genotyping array 2021-03-29 32771030 Tangtanatakul P 2020-08-08 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/32771030 Meta-analysis of genome-wide association study identifies FBN2 as a novel locus associated with systemic lupus erythematosus in Thai population. Systemic lupus erythematosus 487 Thai cases, 1,606 Thai controls 405 Thai cases, 1,590 Thai controls Illumina [421909] (imputed) 38 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST011426 Genome-wide genotyping array 2021-03-22 32740585 Sood RF 2020-08-01 Plast Reconstr Surg www.ncbi.nlm.nih.gov/pubmed/32740585 Genetic Risk of Trigger Finger: Results of a Genomewide Association Study. Trigger finger 942 European ancestry cases, 24,472 European ancestry controls NA Illumina [7846471] (imputed) 3 stenosing tenosynovitis http://www.ebi.ac.uk/efo/EFO_0010822 GCST011318 Genome-wide genotyping array 2020-06-19 23593153 Huertas-Vazquez A 2013-04-04 PLoS One www.ncbi.nlm.nih.gov/pubmed/23593153 Novel loci associated with increased risk of sudden cardiac death in the context of coronary artery disease. Sudden cardiac arrest in coronary artery disease 948 European ancestry cases, 3,050 European ancestry controls NA Illumina [119117] 2 sudden cardiac arrest http://www.ebi.ac.uk/efo/EFO_0004278 GCST010089 Targeted genotyping array [Metabochip] 2021-05-24 32753590 Park B 2020-08-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/32753590 Effect of 6p21 region on lung function is modified by smoking: a genome-wide interaction study. FEV1/FVC ratio x pack-years of smoking interaction (2df test) 1,140 Korean ancestry former smokers, 1,565 Korean ancestry current smokers, 4,768 Korean ancestry controls 65 Korean ancestry former smokers, 592 Korean ancestry current smokers, 2,889 Korean ancestry controls Affymetrix [3351033] (imputed) 0 pack-years measurement, FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0006526, http://www.ebi.ac.uk/efo/EFO_0004713 GCST011718 Genome-wide genotyping array 2021-02-03 32599975 Bae JS 2020-06-30 Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/32599975 Genome-Wide Association Study for the Identification of Novel Genetic Variants Associated with the Risk of Neuroblastoma in Korean Children. Neuroblastoma (pediatric) 296 Korean ancestry child cases, 1,000 Korean ancestry adult controls NA Illumina [NR] (imputed) 14 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST011053 Genome-wide genotyping array 2020-07-07 32489964 Cresci S 2020-01-03 J Lipid Atheroscler www.ncbi.nlm.nih.gov/pubmed/32489964 Genetic Architecture of Circulating Very-Long-Chain (C24:0 and C22:0) Ceramide Concentrations. Ceramide levels (C24:0) 2,217 European ancestry individuals NA Affymetrix [9346801] (imputed) 14 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST010121 Genome-wide genotyping array 2020-07-07 32489964 Cresci S 2020-01-03 J Lipid Atheroscler www.ncbi.nlm.nih.gov/pubmed/32489964 Genetic Architecture of Circulating Very-Long-Chain (C24:0 and C22:0) Ceramide Concentrations. Ceramide levels (C22:0) 2,217 European ancestry individuals NA Affymetrix [9346801] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST010122 Genome-wide genotyping array 2018-11-29 27864402 Harris SE 2017-06-01 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/27864402 Molecular genetic contributions to self-rated health. Self-rated health 111,749 British ancestry individuals NA Affymetrix [~ 17300000] (imputed) 13 self rated health http://www.ebi.ac.uk/efo/EFO_0004778 GCST006620 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Ovarian cancer 720 Japanese ancestry cases, 89,731 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90013704 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pancreatic cancer 442 Japanese ancestry cases, 195,745 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90013705 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Prostate cancer 5,408 Japanese ancestry cases, 103,939 Japanese ancestry controls NA Illumina [8919992] (imputed) 32 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90013706 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Arrhythmia 17,861 Japanese ancestry cases, 194,592 Japanese ancestry controls NA Illumina [8919992] (imputed) 26 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90013707 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cataracts 24,622 Japanese ancestry cases, 187,831 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90013708 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic obstructive pulmonary disease 3,315 Japanese ancestry cases, 201,592 Japanese ancestry controls NA Illumina [8919992] (imputed) 7 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90013709 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cirrhosis 2,184 Japanese ancestry cases, 210,269 Japanese ancestry controls NA Illumina [8919992] (imputed) 2 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90013710 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Endometriosis 734 Japanese ancestry cases, 102,372 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90013711 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Epilepsy 2,143 Japanese ancestry cases, 210,310 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90013712 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Glaucoma 5,761 Japanese ancestry cases, 206,692 Japanese ancestry controls NA Illumina [8919992] (imputed) 6 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90013713 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Interstitial lung disease 806 Japanese ancestry cases, 211,647 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90013714 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Keloid 812 Japanese ancestry cases, 211,641 Japanese ancestry controls NA Illumina [8919992] (imputed) 5 Keloid http://www.ebi.ac.uk/efo/EFO_0004212 GCST90013715 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Nephrotic syndrome 957 Japanese ancestry cases, 211,496 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90013716 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Osteoporosis 7,788 Japanese ancestry cases, 204,665 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90013717 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Periodontal disease 3,219 Japanese ancestry cases, 209,234 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90013718 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Urolithiasis 6,638 Japanese ancestry cases, 205,815 Japanese ancestry controls NA Illumina [8919992] (imputed) 11 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90013719 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Uterine fibroids 5,954 Japanese ancestry cases, 95,010 Japanese ancestry controls NA Illumina [8919992] (imputed) 4 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90013720 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Asthma 3,932 Japanese ancestry male cases, 103,089 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90013721 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Atopic dermatitis 1,262 Japanese ancestry male cases, 107,862 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90013722 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Drug eruption 230 Japanese ancestry male cases, 107,862 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90013723 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pollinosis 2,460 Japanese ancestry male cases, 106,887 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90013724 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Graves' disease 597 Japanese ancestry male cases, 108,750 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST90013725 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Rheumatoid arthritis 874 Japanese ancestry male cases, 108,473 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90013726 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cerebral aneurysm 1,002 Japanese ancestry male cases, 97,455 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90013727 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Congestive heart failure 5,904 Japanese ancestry male cases, 103,443 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 congestive heart failure http://www.ebi.ac.uk/efo/EFO_0000373 GCST90013728 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Coronary artery disease 21,611 Japanese ancestry male cases, 87,736 Japanese ancestry male controls NA Illumina [8919992] (imputed) 1 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90013729 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Ischemic stroke 11,081 Japanese ancestry male cases, 97,455 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90013730 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Peripheral artery disease 2,784 Japanese ancestry male cases, 106,563 Japanese ancestry male controls NA Illumina [8919992] (imputed) 1 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90013731 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic hepatitis B infection 878 Japanese ancestry male cases, 108,469 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST90013732 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic hepatitis C infection 3,159 Japanese ancestry male cases, 106,188 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST90013733 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pulmonary tuberculosis 387 Japanese ancestry male cases, 108,960 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90013734 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Type 2 diabetes 25,705 Japanese ancestry male cases, 82,774 Japanese ancestry male controls NA Illumina [8919992] (imputed) 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90013735 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Biliary tract cancer 211 Japanese ancestry male cases, 97,655 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 biliary tract cancer http://purl.obolibrary.org/obo/MONDO_0003060 GCST90013736 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Colorectal cancer 4,496 Japanese ancestry male cases, 97,655 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90013737 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Esophageal cancer 1,132 Japanese ancestry male cases, 97,655 Japanese ancestry male controls NA Illumina [8919992] (imputed) 1 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST90013738 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Gastric cancer 4,885 Japanese ancestry male cases, 97,655 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90013739 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Hematological malignancy 701 Japanese ancestry male cases, 108,646 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 hematopoietic and lymphoid system neoplasm http://purl.obolibrary.org/obo/MONDO_0002334 GCST90013740 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Hepatocellular carcinoma 1,384 Japanese ancestry male cases, 97,655 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90013741 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Lung cancer 2,710 Japanese ancestry male cases, 106,637 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90013742 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pancreatic cancer 288 Japanese ancestry male cases, 97,655 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90013743 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Arrhythmia 11,525 Japanese ancestry male cases, 97,822 Japanese ancestry male controls NA Illumina [8919992] (imputed) 1 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90013744 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cataracts 11,641 Japanese ancestry male cases, 97,706 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90013745 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic obstructive pulmonary disease 2,855 Japanese ancestry male cases, 103,089 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90013746 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cirrhosis 1,347 Japanese ancestry male cases, 108,000 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90013747 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Epilepsy 1,266 Japanese ancestry male cases, 108,081 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90013748 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Glaucoma 2,770 Japanese ancestry male cases, 106,577 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90013749 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Interstitial lung disease 495 Japanese ancestry male cases, 108,852 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90013750 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Keloid 323 Japanese ancestry male cases, 109,024 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 Keloid http://www.ebi.ac.uk/efo/EFO_0004212 GCST90013751 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Nephrotic syndrome 583 Japanese ancestry male cases, 108,764 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90013752 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Osteoporosis 696 Japanese ancestry male cases, 108,651 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90013753 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Periodontal disease 1,415 Japanese ancestry male cases, 107,932 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90013754 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Urolithiasis 4,996 Japanese ancestry male cases, 104,351 Japanese ancestry male controls NA Illumina [8919992] (imputed) 0 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90013755 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Asthma 4,284 Japanese ancestry female cases, 98,503 Japanese ancestry female controls NA Illumina [8919992] (imputed) 2 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90013756 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Atopic dermatitis 1,123 Japanese ancestry female cases, 101,789 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90013757 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Drug eruption 200 Japanese ancestry female cases, 101,789 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90013758 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pollinosis 3,286 Japanese ancestry female cases, 99,820 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90013759 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Graves' disease 1,579 Japanese ancestry female cases, 101,527 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST90013760 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Rheumatoid arthritis 3,325 Japanese ancestry female cases, 99,781 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90013761 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cerebral aneurysm 1,818 Japanese ancestry female cases, 94,928 Japanese ancestry female controls NA Illumina [8919992] (imputed) 1 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90013762 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Congestive heart failure 3,509 Japanese ancestry female cases, 99,597 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 congestive heart failure http://www.ebi.ac.uk/efo/EFO_0000373 GCST90013763 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Coronary artery disease 7,708 Japanese ancestry female cases, 95,398 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90013764 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Ischemic stroke 6,590 Japanese ancestry female cases, 94,928 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90013765 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Peripheral artery disease 809 Japanese ancestry female cases, 102,297 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90013766 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic hepatitis B infection 516 Japanese ancestry female cases, 102,590 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST90013767 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic hepatitis C infection 2,635 Japanese ancestry female cases, 100,471 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST90013768 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pulmonary tuberculosis 162 Japanese ancestry female cases, 102,944 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90013769 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Type 2 diabetes 14,545 Japanese ancestry female cases, 87,841 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90013770 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Biliary tract cancer 128 Japanese ancestry female cases, 98,090 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 biliary tract cancer http://purl.obolibrary.org/obo/MONDO_0003060 GCST90013771 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Colorectal cancer 2,566 Japanese ancestry female cases, 98,090 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90013772 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Esophageal cancer 168 Japanese ancestry female cases, 98,090 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST90013773 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Gastric cancer 1,678 Japanese ancestry female cases, 98,090 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90013774 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Hematological malignancy 535 Japanese ancestry female cases, 102,571 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 hematopoietic and lymphoid system neoplasm http://purl.obolibrary.org/obo/MONDO_0002334 GCST90013775 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Hepatocellular carcinoma 482 Japanese ancestry female cases, 98,090 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90013776 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Lung cancer 1,340 Japanese ancestry female cases, 101,766 Japanese ancestry female controls NA Illumina [8919992] (imputed) 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90013777 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pancreatic cancer 154 Japanese ancestry female cases, 98,090 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90013778 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Arrhythmia 6,336 Japanese ancestry female cases, 96,770 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90013779 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cataracts 12,981 Japanese ancestry female cases, 90,125 Japanese ancestry female controls NA Illumina [8919992] (imputed) 1 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90013780 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic obstructive pulmonary disease 460 Japanese ancestry female cases, 98,503 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90013781 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cirrhosis 837 Japanese ancestry female cases, 102,269 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90013782 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Epilepsy 877 Japanese ancestry female cases, 102,229 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90013783 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Glaucoma 2,991 Japanese ancestry female cases, 100,115 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90013784 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Interstitial lung disease 311 Japanese ancestry female cases, 102,795 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90013785 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Keloid 489 Japanese ancestry female cases, 102,617 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 Keloid http://www.ebi.ac.uk/efo/EFO_0004212 GCST90013786 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Nephrotic syndrome 374 Japanese ancestry female cases, 102,732 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90013787 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Osteoporosis 7,092 Japanese ancestry female cases, 96,014 Japanese ancestry female controls NA Illumina [8919992] (imputed) 1 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90013788 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Periodontal disease 1,804 Japanese ancestry female cases, 101,302 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90013789 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Urolithiasis 1,642 Japanese ancestry female cases, 101,464 Japanese ancestry female controls NA Illumina [8919992] (imputed) 0 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90013790 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Asthma 8,216 Japanese ancestry cases, 201,592 Japanese ancestry controls NA Illumina [8919992] (imputed) 13 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90013679 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Atopic dermatitis 2,385 Japanese ancestry cases, 209,651 Japanese ancestry controls NA Illumina [8919992] (imputed) 7 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90013680 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Drug eruption 430 Japanese ancestry cases, 209,651 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90013681 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pollinosis 5,746 Japanese ancestry cases, 206,707 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90013682 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Graves' disease 2,176 Japanese ancestry cases, 210,277 Japanese ancestry controls NA Illumina [8919992] (imputed) 11 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST90013683 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Rheumatoid arthritis 4,199 Japanese ancestry cases, 208,254 Japanese ancestry controls NA Illumina [8919992] (imputed) 6 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90013684 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cerebral aneurysm 2,820 Japanese ancestry cases, 192,383 Japanese ancestry controls NA Illumina [8919992] (imputed) 5 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90013685 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Congestive heart failure 9,413 Japanese ancestry cases, 203,040 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 congestive heart failure http://www.ebi.ac.uk/efo/EFO_0000373 GCST90013686 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Coronary artery disease 29,319 Japanese ancestry cases, 183,134 Japanese ancestry controls 2,855 Japanese ancestry cases, 15,211 Japanese ancestry controls Illumina [8919992] (imputed) 3 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90013687 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Ischemic stroke 17,671 Japanese ancestry cases, 192,383 Japanese ancestry controls NA Illumina [8919992] (imputed) 3 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90013688 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Peripheral artery disease 3,593 Japanese ancestry cases, 208,860 Japanese ancestry controls NA Illumina [8919992] (imputed) 3 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90013689 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic hepatitis B infection 1,394 Japanese ancestry cases, 211,059 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST90013690 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Chronic hepatitis C infection 5,794 Japanese ancestry cases, 206,659 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST90013691 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Pulmonary tuberculosis 549 Japanese ancestry cases, 211,904 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90013692 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Type 2 diabetes 40,250 Japanese ancestry cases, 170,615 Japanese ancestry controls NA Illumina [8919992] (imputed) 129 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90013693 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Biliary tract cancer 339 Japanese ancestry cases, 195,745 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 biliary tract cancer http://purl.obolibrary.org/obo/MONDO_0003060 GCST90013694 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Breast cancer 5,552 Japanese ancestry cases, 89,731 Japanese ancestry controls NA Illumina [8919992] (imputed) 9 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90013695 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Cervical cancer 605 Japanese ancestry cases, 89,731 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90013696 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Colorectal cancer 7,062 Japanese ancestry cases, 195,745 Japanese ancestry controls NA Illumina [8919992] (imputed) 14 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90013697 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Endometrial cancer 999 Japanese ancestry cases, 89,731 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST90013698 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Esophageal cancer 1,300 Japanese ancestry cases, 195,745 Japanese ancestry controls NA Illumina [8919992] (imputed) 2 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST90013699 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Gastric cancer 6,563 Japanese ancestry cases, 195,745 Japanese ancestry controls NA Illumina [8919992] (imputed) 5 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90013700 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Hematological malignancy 1,236 Japanese ancestry cases, 211,217 Japanese ancestry controls NA Illumina [8919992] (imputed) 0 hematopoietic and lymphoid system neoplasm http://purl.obolibrary.org/obo/MONDO_0002334 GCST90013701 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Hepatocellular carcinoma 1,866 Japanese ancestry cases, 195,745 Japanese ancestry controls NA Illumina [8919992] (imputed) 1 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90013702 Genome-wide genotyping array 2021-02-26 32514122 Ishigaki K 2020-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32514122 Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases. Lung cancer 4,050 Japanese ancestry cases, 208,403 Japanese ancestry controls 2,440 Japanese ancestry cases, 467 Japanese ancestry controls Illumina [8919992] (imputed) 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90013703 Genome-wide genotyping array 2021-03-22 32737115 Shirai Y 2020-07-31 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/32737115 Association of the RPA3-UMAD1 locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese. Interstitial lung diseases in rheumatoid arthritis 358 Japanese ancestry cases, 4,550 Japanese ancestry controls NA Illumina [5934489] (imputed) 11 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST011319 Genome-wide genotyping array 2019-05-10 30711515 Hallberg P 2019-01-30 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/30711515 Pandemrix-induced narcolepsy is associated with genes related to immunity and neuronal survival. Pandemrix-induced narcolepsy 41 European ancestry cases, 1 case, 4,891 European ancestry controls 31 European ancestry cases, 1 case, 7,125 European and other ancestry controls Illumina [8600000] (imputed) 0 narcolepsy, response to vaccine http://purl.obolibrary.org/obo/MONDO_0021107, http://www.ebi.ac.uk/efo/EFO_0004645 GCST007779 Genome-wide genotyping array 2021-01-26 32376654 Richardson TG 2020-05-06 BMJ www.ncbi.nlm.nih.gov/pubmed/32376654 Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study. Body size at age 10 453,169 European ancestry individuals NA Affymetrix [12370749] 291 comparative body size at age 10, self-reported http://www.ebi.ac.uk/efo/EFO_0009819 GCST010989 Genome-wide genotyping array 2021-01-26 32376654 Richardson TG 2020-05-06 BMJ www.ncbi.nlm.nih.gov/pubmed/32376654 Use of genetic variation to separate the effects of early and later life adiposity on disease risk: mendelian randomisation study. Adult body size 453,169 European ancestry individuals Affymetrix [12370749] 554 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST010988 Genome-wide genotyping array 2018-10-17 30181573 Jing J 2018-09-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30181573 Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease. Serum urate levels in chronic kidney disease 4,941 European ancestry cases NA Illumina [9281895] (imputed) 7 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST006426 Genome-wide genotyping array 2018-10-17 30181573 Jing J 2018-09-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30181573 Genetics of serum urate concentrations and gout in a high-risk population, patients with chronic kidney disease. Gout in chronic kidney disease 1,217 European ancestry cases, 3,724 European ancestry controls NA Illumina [9281895] (imputed) 2 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST006425 Genome-wide genotyping array 2021-01-25 33115937 Cho J 2020-10-28 Thorax www.ncbi.nlm.nih.gov/pubmed/33115937 Genome-wide association study of non-tuberculous mycobacterial pulmonary disease. Non-tuberculous mycobacterial pulmonary disease 403 Korean ancestry cases, 306 Korean ancestry controls 184 Korean ancestry cases, 1680 Korean ancestry controls Illumina [4877242] (imputed) 11 pulmonary non-tuberculous mycobacterial infection http://purl.obolibrary.org/obo/MONDO_0018469 GCST010983 Genome-wide genotyping array 2019-11-11 27453504 Rhee EP 2016-07-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27453504 An exome array study of the plasma metabolome. Blood metabolite levels 2,076 European ancestry individuals 1,528 European ancestry individuals Illumina [81021] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST009018 Exome genotyping array [Exome array] 2021-03-24 33597508 Coignard J 2021-02-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33597508 A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers. BRCA1 mutation in breast cancer 7,257 European ancestry cases, 60,212 European ancestry controls NA Illumina [9068301] (imputed) 13 BRCA1 mutation carier status http://www.ebi.ac.uk/efo/EFO_0011021 GCST011402 Genome-wide genotyping array 2021-03-24 33597508 Coignard J 2021-02-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33597508 A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers. BRCA2 mutation in breast cancer 5,097 European ancestry cases, 57,725 European ancestry controls NA Illumina [9043830] (imputed) 10 BRCA2 mutation carier statu http://www.ebi.ac.uk/efo/EFO_0011022 GCST011401 Genome-wide genotyping array 2021-03-24 33597508 Coignard J 2021-02-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33597508 A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers. BRCA1 mutation in healthy women 5,750 European ancestry cases, 45,881 European ancestry controls NA Illumina [NR] (imputed) 0 BRCA1 mutation carier status http://www.ebi.ac.uk/efo/EFO_0011021 GCST011400 Genome-wide genotyping array 2021-03-24 33597508 Coignard J 2021-02-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33597508 A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers. BRCA2 mutation in healthy women 4,456 European ancestry cases, 43,549 European ancestry controls NA Illumina [NR] (imputed) 0 BRCA2 mutation carier statu http://www.ebi.ac.uk/efo/EFO_0011022 GCST011399 Genome-wide genotyping array 2021-03-22 33594131 Donati G 2021-02-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33594131 Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence. Academic attainment (English) 5,983 European ancestry adolescents NA Illumina [6319684] (imputed) 16 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST011358 Genome-wide genotyping array 2021-03-22 33594131 Donati G 2021-02-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33594131 Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence. Academic attainment (maths) 6,017 European ancestry adolescents NA Illumina [6319684] (imputed) 38 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST011357 Genome-wide genotyping array 2021-03-22 33594131 Donati G 2021-02-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33594131 Evidence for specificity of polygenic contributions to attainment in English, maths and science during adolescence. Academic attainment (science) 6,089 European ancestry adolescents NA Illumina [6319684] (imputed) 27 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST011356 Genome-wide genotyping array 2021-08-10 33607655 Imamura M 2021-02-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33607655 Genome-Wide Association Studies Identify Two Novel Loci Conferring Susceptibility to Diabetic Retinopathy in Japanese Patients with Type 2 Diabetes. Diabetic retinopathy in type 2 diabetes 5,532 Japanese ancestry cases, 5,565 Japanese ancestry controls 3,010 Japanese ancestry cases, 1,562 Japanese ancestry controls Illumina [5790508] (imputed) 6 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST012174 Genome-wide genotyping array 2021-07-27 33495439 Demontis D 2021-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33495439 Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Disruptive behavior disorder in attention deficit hyperactivity disorder 1,959 European ancestry cases, 13,539 European ancestry controls NA Illumina [NR] 0 conduct disorder, Oppositional defiant disorder http://www.ebi.ac.uk/efo/EFO_0004216, http://purl.obolibrary.org/obo/HP_0010865 GCST012097 Genome-wide genotyping array 2021-07-27 33495439 Demontis D 2021-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33495439 Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Attention deficit hyperactivity disorder 13,583 European ancestry cases, 22,314 European ancestry controls NA Illumina [NR] 1 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST012096 Genome-wide genotyping array 2021-07-27 33495439 Demontis D 2021-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33495439 Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder. Disruptive behavior disorder and attention deficit hyperactivity disorder 3,802 European ancestry cases, 31,305 European ancestry controls, 406 Han Chinese ancestry cases, 917 Han Chinese ancestry controls NA Affymetrix, Illumina, Perlegen [8285688] (imputed) 3 attention deficit hyperactivity disorder, conduct disorder, Oppositional defiant disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004216, http://purl.obolibrary.org/obo/HP_0010865 GCST012098 Genome-wide genotyping array 2021-07-28 33095540 Sherman BT 2020-10-20 AIDS www.ncbi.nlm.nih.gov/pubmed/33095540 Genome-wide association study of high-sensitivity C-reactive protein, D-dimer and Interleukin-6 levels in multi-ethnic HIV+ cohorts. D-dimer levels in HIV infection 4,675 European ancestry individuals, 1,732 African ancestry individuals, 645 Admixed American individuals NA Affymetrix [up to 12642786] (imputed) 5 D dimer measurement http://www.ebi.ac.uk/efo/EFO_0004507 GCST012139 Genome-wide genotyping array 2021-07-28 33095540 Sherman BT 2020-10-20 AIDS www.ncbi.nlm.nih.gov/pubmed/33095540 Genome-wide association study of high-sensitivity C-reactive protein, D-dimer and Interleukin-6 levels in multi-ethnic HIV+ cohorts. Interleukin-6 levels in HIV infection 4,675 European ancestry individuals, 1,732 African ancestry individuals, 645 Admixed American individuals NA Affymetrix [up to 12642786] (imputed) 3 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST012138 Genome-wide genotyping array 2021-07-28 33095540 Sherman BT 2020-10-20 AIDS www.ncbi.nlm.nih.gov/pubmed/33095540 Genome-wide association study of high-sensitivity C-reactive protein, D-dimer and Interleukin-6 levels in multi-ethnic HIV+ cohorts. High-sensitivity C-reactive protein levels in HIV infection 4,675 European ancestry individuals, 1,732 African ancestry individuals, 645 Admixed American individuals NA Affymetrix [up to 12642786] (imputed) 4 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST012140 Genome-wide genotyping array 2019-04-05 30657218 Park SY 2019-01-18 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/30657218 Longitudinal analysis to better characterize Asthma-COPD Overlap Syndrome (ACOS): Findings from an adult asthma cohort in Korea (COREA). Adult asthma 731 Korean ancestry cases, 5,915 Korean ancestry controls NA NR [267429] 2 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007519 Genome-wide genotyping array 2019-04-05 30657218 Park SY 2019-01-18 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/30657218 Longitudinal analysis to better characterize Asthma-COPD Overlap Syndrome (ACOS): Findings from an adult asthma cohort in Korea (COREA). Asthma-chronic obstructive pulmonary disease overlap syndrome in asthma 228 Korean ancestry asthma-COPD overlap syndrome cases, 731 Korean ancestry asthma cases NA NR [267429] 0 Chronic Obstructive Asthma http://www.ebi.ac.uk/efo/EFO_0009759 GCST007520 Genome-wide genotyping array 2019-04-05 30657218 Park SY 2019-01-18 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/30657218 Longitudinal analysis to better characterize Asthma-COPD Overlap Syndrome (ACOS): Findings from an adult asthma cohort in Korea (COREA). Asthma-chronic obstructive pulmonary disease overlap syndrome 228 Korean ancestry cases, 5,915 Korean ancestry controls NA Korean Chip 5 Chronic Obstructive Asthma http://www.ebi.ac.uk/efo/EFO_0009759 GCST007521 Genome-wide genotyping array 2019-06-26 28265093 Malik R 2017-03-06 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/28265093 Common coding variant in SERPINA1 increases the risk for large artery stroke. Large artery stroke up to 2,286 European ancestry cases, up to 376 South Asian cases, up to 8,884 European ancestry controls, up to 978 South Asian controls NA Illumina [92772] 8 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST007991 Exome genotyping array [Exome array] 2021-02-03 33398198 Conti DV 2021-01-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33398198 Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction. Prostate cancer 85,554 European ancestry cases, 10,368 African ancestry cases, 8,611 East Asian ancestry cases, 2,714 Hispanic cases, 91,972 European ancestry controls, 10,986 African ancestry controls, 18,809 East Asian ancestry controls, 5,239 Hispanic controls NA Affymetrix, Illumina [29235255] (imputed) 264 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011049 Genome-wide genotyping array 2021-02-03 33398198 Conti DV 2021-01-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33398198 Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction. Prostate cancer 85,554 European ancestry cases, 91,972 European ancestry controls 6,852 European ancestry cases, 193,117 European ancestry controls Affymetrix, Illumina [20400945] (imputed) 64 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011048 Genome-wide genotyping array 2021-02-03 33398198 Conti DV 2021-01-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33398198 Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction. Prostate cancer 10,368 African ancestry cases, 10,986 African ancestry controls NA Affymetrix, Illumina [18877980] (imputed) 20 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011047 Genome-wide genotyping array 2021-02-03 33398198 Conti DV 2021-01-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33398198 Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction. Prostate cancer 8,611 East Asian ancestry cases, 18,809 East Asian ancestry controls NA Affymetrix, Illumina [10186136] (imputed) 48 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011046 Genome-wide genotyping array 2021-02-03 33398198 Conti DV 2021-01-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33398198 Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction. Prostate cancer 2,714 Hispanic cases, 5,239 Hispanic controls NA Affymetrix, Illumina [11334207] (imputed) 4 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011045 Genome-wide genotyping array 2021-02-11 33338681 Chu H 2020-12-15 Environ Int www.ncbi.nlm.nih.gov/pubmed/33338681 A prospective study of the associations among fine particulate matter, genetic variants, and the risk of colorectal cancer. Colorectal cancer x fine particulate matter exposure levels interaction 590 European ancestry cases, 55 Black cases, 9 Hispanic cases, 28 Asian ancestry cases, 5 cases, 12,715 European ancestry controls, 1,153 Black controls, 37 Hispanic controls, 94 Asian ancestry controls, 15 controls NA Illumina [4085111] (imputed) 5 colorectal cancer, particulate matter air pollution measurement http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0008255 GCST011108 Genome-wide genotyping array 2019-02-20 30338293 Wallen ZD 2018-10-05 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/30338293 Plasticity-related gene 3 (LPPR1) and age at diagnosis of Parkinson disease. Parkinson's disease (age at diagnosis) 1,950 European ancestry cases 726 European ancestry cases Illumina [8500000] (imputed) 1 age at diagnosis, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0005180 GCST007198 Genome-wide genotyping array 2020-02-26 31841133 Chen G 2019-12-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31841133 Refining genome-wide associated loci for serum uric acid in individuals with African ancestry. Serum uric acid levels 4,126 African ancestry individuals, 5,007 African American individuals NA Affymetrix, Illumina [up to 18219730] (imputed) 4 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST009699 Genome-wide genotyping array 2020-01-22 31641590 Stevelink R 2019-10-11 Mol Genet Metab Rep www.ncbi.nlm.nih.gov/pubmed/31641590 Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. Pyridoxal 5'-phosphate levels 2,232 Irish ancestry individuals NA NR [~ 6000000] (imputed) 2 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST009471 Genome-wide genotyping array 2020-01-22 31641590 Stevelink R 2019-10-11 Mol Genet Metab Rep www.ncbi.nlm.nih.gov/pubmed/31641590 Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. Plasma pyridoxal phosphate to pyridoxal ratio 2,232 Irish ancestry individuals NA NR [~ 6000000] (imputed) 2 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST009470 Genome-wide genotyping array 2020-01-22 31641590 Stevelink R 2019-10-11 Mol Genet Metab Rep www.ncbi.nlm.nih.gov/pubmed/31641590 Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. Pyridoxal levels 2,232 Irish ancestry individuals NA NR [~ 6000000] (imputed) 1 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST009469 Genome-wide genotyping array 2020-01-22 31641590 Stevelink R 2019-10-11 Mol Genet Metab Rep www.ncbi.nlm.nih.gov/pubmed/31641590 Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. 4-pyridoxic acid levels 2,232 Irish ancestry individuals NA NR [~ 6000000] (imputed) 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST009472 Genome-wide genotyping array 2020-01-22 31641590 Stevelink R 2019-10-11 Mol Genet Metab Rep www.ncbi.nlm.nih.gov/pubmed/31641590 Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy. PAr index (pyridoxic acid/(pyridoxal 5′-phosphate + pyridoxal)) 2,232 Irish ancestry individuals NA NR [~ 6000000] (imputed) 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST009473 Genome-wide genotyping array 2020-03-09 31862735 Karsai G 2019-12-20 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/31862735 FADS3 is a delta14Z sphingoid base desaturase that contributes to gender differences to the human plasma sphingolipidome. Sphingolipid d18:1/d18:2 ratio 658 European ancestry individuals NA NR [2557249] (imputed) 1 sphingolipid measurement http://www.ebi.ac.uk/efo/EFO_0004622 GCST009756 Genome-wide genotyping array 2019-06-18 30866520 Er LK 2019-03-07 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/30866520 Circulating Chemerin Levels, but not the RARRES2 Polymorphisms, Predict the Long-Term Outcome of Angiographically Confirmed Coronary Artery Disease. Chemerin levels 2,197 Taiwanese individuals NA Affymetrix [614820] 1 chemerin measurement http://www.ebi.ac.uk/efo/EFO_0004573 GCST007900 Genome-wide genotyping array 2021-08-13 33597122 Verbitsky M 2021-02-17 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/33597122 Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux. Vesicoureteral reflux 1,395 European ancestry cases, 5,366 European ancestry controls NA Affymetrix, Illumina [6131010] (imputed) 32 vesicoureteral reflux http://www.ebi.ac.uk/efo/EFO_0007536 GCST012183 Genome-wide genotyping array 2021-07-28 33500527 Park JM 2021-01-26 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33500527 Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population. Metabolically unhealthy in obesity 9,083 Korean ancestry cases, 7,008 Korean ancestry controls NA Affymetrix [7975321] 3 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST012148 Genome-wide genotyping array 2021-07-28 33500527 Park JM 2021-01-26 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33500527 Understanding the genetic architecture of the metabolically unhealthy normal weight and metabolically healthy obese phenotypes in a Korean population. Metabolically unhealthy in normal weight 10,358 Korean ancestry cases, 23,466 Korean ancestry controls NA Affymetrix [7975321] 9 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST012149 Genome-wide genotyping array 2021-03-01 33574239 Eriksson D 2021-02-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33574239 GWAS for autoimmune Addison's disease identifies multiple risk loci and highlights AIRE in disease susceptibility. Addison's disease 1,223 European ancestry cases, 4,097 European ancestry controls NA Illumina [7068382] (imputed) 10 Genetic chronic primary adrenal insufficiency http://www.orpha.net/ORDO/Orphanet_101960 GCST90011871 Genome-wide genotyping array 2021-04-20 33587031 Sinnott-Armstrong N 2021-02-15 Elife www.ncbi.nlm.nih.gov/pubmed/33587031 GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background. Urate levels 318,526 British ancestry individuals NA NR [16000000] (imputed) 299 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST011521 Genome-wide genotyping array 2021-04-20 33587031 Sinnott-Armstrong N 2021-02-15 Elife www.ncbi.nlm.nih.gov/pubmed/33587031 GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background. Insulin-like growth factor 1 levels 317,114 British ancestry individuals NA NR [16000000] (imputed) 402 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST011520 Genome-wide genotyping array 2021-04-20 33587031 Sinnott-Armstrong N 2021-02-15 Elife www.ncbi.nlm.nih.gov/pubmed/33587031 GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background. Testosterone levels 142,778 British ancestry women NA NR [16000000] (imputed) 79 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST011519 Genome-wide genotyping array 2021-04-20 33587031 Sinnott-Armstrong N 2021-02-15 Elife www.ncbi.nlm.nih.gov/pubmed/33587031 GWAS of three molecular traits highlights core genes and pathways alongside a highly polygenic background. Testosterone levels 146,339 British ancestry men NA NR [16000000] (imputed) 130 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST011518 Genome-wide genotyping array 2018-06-29 29650774 Rotroff DM 2018-04-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/29650774 Genetic Variants in CPA6 and PRPF31 are Associated with Variation in Response to Metformin in Individuals with Type 2 Diabetes. Change in HbA1c levels in response to metformin treatment in type 2 diabetes 845 European ancestry individuals, 222 African American individuals, 245 individuals 6,963 European ancestry individuals, 1,015 African American individuals, 4,520 individuals Affymetrix, Illumina [26000000] (imputed) 1 HbA1c measurement, response to metformin http://www.ebi.ac.uk/efo/EFO_0004541, http://purl.obolibrary.org/obo/GO_1901558 GCST005753 Genome-wide genotyping array 2019-05-20 30837455 Dudding T 2019-03-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30837455 Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci. Mouth ulcers 47,079 British or unknown ancestry cases, 414,027 British or unknown ancestry controls 98,298 cases, 247,446 controls Affymetrix, Illumina [9851866] (imputed) 94 Oral ulcer http://purl.obolibrary.org/obo/HP_0000155 GCST007839 Genome-wide genotyping array 2021-03-02 33593824 Wang YN 2021-02-16 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/33593824 Interaction between G ALNT12 and C1GALT1 Associates with Galactose-Deficient IgA1 and IgA Nephropathy. Serum galactose-deficient IgA1 levels in IgA nephropathy 849 Han Chinese ancestry individuals 313 Han Chinese ancestry individuals Illumina [5737162] (imputed) 2 serum galactose-deficient IgA1 measurement http://www.ebi.ac.uk/efo/EFO_0007947 GCST90011884 Genome-wide genotyping array 2021-07-19 33479058 Srinivasan S 2021-01-21 Diabetes www.ncbi.nlm.nih.gov/pubmed/33479058 The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium. Childhood onset type 2 diabetes 664 European ancestry youth cases, 1,068 African American youth cases, 1,274 Hispanic youth cases, 1,434 European ancestry adult controls, 1,068 African American adult controls, 3,559 Hispanic adult controls NA Illumina [10000000] (imputed) 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST012043 Genome-wide genotyping array 2021-07-19 33479058 Srinivasan S 2021-01-21 Diabetes www.ncbi.nlm.nih.gov/pubmed/33479058 The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium. Type 2 diabetes 664 European ancestry youth cases, 1,068 African American youth cases, 1,274 Hispanic youth cases, 542 European ancestry youth controls, 314 African American youth controls NA Illumina [~ 10000000] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST012042 Genome-wide genotyping array 2018-12-14 30336701 Sanchez-Roige S 2018-10-19 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30336701 Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. Alcohol use disorder (total score) 141,932 European ancestry individuals NA NR [16213998] 15 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST006716 Genome-wide genotyping array 2018-12-14 30336701 Sanchez-Roige S 2018-10-19 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30336701 Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. Alcohol use disorder (consumption score) 121,604 British ancestry individuals NA NR [16213998] 9 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST006718 Genome-wide genotyping array 2018-12-14 30336701 Sanchez-Roige S 2018-10-19 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30336701 Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. Alcohol use disorder (dependence and problematic use scores) 121,604 British ancestry individuals NA NR [16213998] 5 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST006717 Genome-wide genotyping array 2018-12-14 30323354 Lee JY 2018-10-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30323354 BRCA1/2-negative, high-risk breast cancers (BRCAX) for Asian women: genetic susceptibility loci and their potential impacts. BRCA1/2-negative high-risk breast cancer 1,469 Korean ancestry cases, 5,979 Korean ancestry controls NA Affymetrix, Illumina [3378933] (imputed) 19 BRCAX breast cancer http://www.ebi.ac.uk/efo/EFO_0009443 GCST006719 Genome-wide genotyping array 2018-10-19 30172743 Liang X 2018-08-30 Bone www.ncbi.nlm.nih.gov/pubmed/30172743 Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis. Total body bone mineral density 2,286 European ancestry individuals NA Affymetrix [753382] 6 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST006443 Genome-wide genotyping array 2018-10-19 30172743 Liang X 2018-08-30 Bone www.ncbi.nlm.nih.gov/pubmed/30172743 Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis. Bone mineral density (hip) 2,286 European ancestry individuals NA Affymetrix [753382] 24 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST006444 Genome-wide genotyping array 2018-10-19 30172743 Liang X 2018-08-30 Bone www.ncbi.nlm.nih.gov/pubmed/30172743 Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis. Femoral neck bone mineral density 2,286 European ancestry individuals NA Affymetrix [753382] 8 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST006445 Genome-wide genotyping array 2018-10-19 30172743 Liang X 2018-08-30 Bone www.ncbi.nlm.nih.gov/pubmed/30172743 Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis. Ulna and radius bone mineral density 2,286 European ancestry individuals NA Affymetrix [753382] 7 radius bone mineral density http://www.ebi.ac.uk/efo/EFO_0007933 GCST006446 Genome-wide genotyping array 2018-10-19 30172743 Liang X 2018-08-30 Bone www.ncbi.nlm.nih.gov/pubmed/30172743 Assessing the genetic correlations between early growth parameters and bone mineral density: A polygenic risk score analysis. Bone mineral density (spine) 2,286 European ancestry individuals NA Affymetrix [753382] 3 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST006447 Genome-wide genotyping array 2020-02-17 31630189 Casanova F 2019-10-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/31630189 A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio. Urinary albumin-to-creatinine ratio 437,027 European ancestry individuals 60,130 individuals NR [12082474] (imputed) 59 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST009640 Genome-wide genotyping array 2020-11-12 33110245 Ruotsalainen SE 2020-10-27 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33110245 An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease. Inflammatory biomarkers (multivariate analysis) 6,890 Finnish ancestry individuals NA Illumina [11329225] (imputed) 16 inflammatory biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004872 GCST90000584 Genome-wide genotyping array 2019-11-20 31125052 Green HD 2019-05-24 J Crohns Colitis www.ncbi.nlm.nih.gov/pubmed/31125052 Genome-wide association study of microscopic colitis in the UK Biobank confirms immune-related pathogenesis. Microscopic colitis in proton-pump inhibitor treatment up to 98 European ancestry cases, up to 46,397 European ancestry controls NA Affymetrix [~ 12000000] (imputed) 0 microscopic colitis, response to proton-pump inhibitor http://www.ebi.ac.uk/efo/EFO_1001295, http://www.ebi.ac.uk/efo/EFO_0010235 GCST009080 Genome-wide genotyping array 2019-11-20 31125052 Green HD 2019-05-24 J Crohns Colitis www.ncbi.nlm.nih.gov/pubmed/31125052 Genome-wide association study of microscopic colitis in the UK Biobank confirms immune-related pathogenesis. Microscopic colitis 423 European ancestry cases, 445,232 European ancestry controls NA Affymetrix [~ 12000000] (imputed) 24 microscopic colitis http://www.ebi.ac.uk/efo/EFO_1001295 GCST009081 Genome-wide genotyping array 2021-07-28 33491795 Timmer T 2021-01-25 Vox Sang www.ncbi.nlm.nih.gov/pubmed/33491795 Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight. Hemoglobin levels 2,649 European ancestry individuals NA Affymetrix [7435577] (imputed) 20 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST012146 Genome-wide genotyping array 2021-07-28 33491795 Timmer T 2021-01-25 Vox Sang www.ncbi.nlm.nih.gov/pubmed/33491795 Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight. Ferritin levels 2,649 European ancestry individuals NA Affymetrix [7435577] (imputed) 24 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST012145 Genome-wide genotyping array 2021-07-28 33491795 Timmer T 2021-01-25 Vox Sang www.ncbi.nlm.nih.gov/pubmed/33491795 Genetic determinants of ferritin, haemoglobin levels and haemoglobin trajectories: results from Donor InSight. Declining hemoglobin trajectory in blood donors 1,044 European ancestry cases, 783 European ancestry controls NA Affymetrix [7435577] (imputed) 12 hemoglobin change measurement http://www.ebi.ac.uk/efo/EFO_0600027 GCST012147 Genome-wide genotyping array 2019-04-30 30843173 Popovic M 2019-03-07 J Endocrinol Invest www.ncbi.nlm.nih.gov/pubmed/30843173 Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone. Triiodothyronine levels 629 Croatian individuals, 510 Korculan (founder/genetic isolate) individuals, 590 Vis (founder/genetic isolate) individuals NA Illumina [7411206] (imputed) 3 triiodothyronine measurement http://www.ebi.ac.uk/efo/EFO_0008392 GCST007683 Genome-wide genotyping array 2019-04-30 30843173 Popovic M 2019-03-07 J Endocrinol Invest www.ncbi.nlm.nih.gov/pubmed/30843173 Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone. Thyroxine levels 596 Croatian individuals, 510 Korculan (founder/genetic isolate) individuals, 609 Vis (founder/genetic isolate) individuals NA Illumina [7411206] (imputed) 4 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST007682 Genome-wide genotyping array 2019-04-30 30843173 Popovic M 2019-03-07 J Endocrinol Invest www.ncbi.nlm.nih.gov/pubmed/30843173 Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone. Thyroid stimulating hormone levels 626 Croatian individuals, 509 Korculan (founder/genetic isolate) individuals, 596 Vis (founder/genetic isolate) individuals NA Illumina [7411206] (imputed) 4 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST007681 Genome-wide genotyping array 2019-04-30 30843173 Popovic M 2019-03-07 J Endocrinol Invest www.ncbi.nlm.nih.gov/pubmed/30843173 Genome-wide meta-analysis identifies novel loci associated with free triiodothyronine and thyroid-stimulating hormone. Triiodothyronine levels and thyroxine levels Up to 1,729 Croatian, Korculan (founder/genetic isolate) and Vis (founder/genetic isolate) individuals NA Illumina [7411206] (imputed) 11 thyroxine measurement, triiodothyronine measurement http://www.ebi.ac.uk/efo/EFO_0005130, http://www.ebi.ac.uk/efo/EFO_0008392 GCST007680 Genome-wide genotyping array 2018-10-18 30120420 Sun R 2018-08-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30120420 Identification of novel loci associated with infant cognitive ability. Motor composite score 502 Bangladeshi ancestry infants, 462 Hispanic or Latin American infants NA Illumina [552487] 5 motor development measurement http://www.ebi.ac.uk/efo/EFO_0008237 GCST006440 Genome-wide genotyping array 2018-10-18 30120420 Sun R 2018-08-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30120420 Identification of novel loci associated with infant cognitive ability. Mental composite score 502 Bangladeshi ancestry infants, 462 Hispanic or Latin American infants NA Illumina [552487] 7 mental development measurement http://www.ebi.ac.uk/efo/EFO_0008230 GCST006441 Genome-wide genotyping array 2021-05-18 33269293 Kannambath S 2020-10-16 Open Forum Infect Dis www.ncbi.nlm.nih.gov/pubmed/33269293 Genome-Wide Association Study Identifies Novel Colony Stimulating Factor 1 Locus Conferring Susceptibility to Cryptococcosis in Human Immunodeficiency Virus-Infected South Africans. Cryptococcosis in HIV infection 319 South African ancestry cases, 399 South African ancestry controls NA Illumina [2686126] (imputed) 8 cryptococcosis http://www.ebi.ac.uk/efo/EFO_0007229 GCST011681 Genome-wide genotyping array 2019-03-21 30202041 Otani T 2018-09-10 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30202041 Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models. Progression-free survival response to gemcitabine in breast cancer 1,621 treated cases, 1,668 untreated cases NA Illumina [424121] 0 progression free survival, response to gemcitabine http://www.ebi.ac.uk/efo/EFO_0004920, http://purl.obolibrary.org/obo/GO_0036272 GCST007365 Genome-wide genotyping array 2019-03-21 30202041 Otani T 2018-09-10 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30202041 Exploring predictive biomarkers from clinical genome-wide association studies via multidimensional hierarchical mixture models. Homocysteine level response to multivitamin in cerebral infarction 760 European ancestry treated cases, 773 European ancestry untreated cases NA Illumina [774670] 0 homocysteine measurement, response to vitamin http://www.ebi.ac.uk/efo/EFO_0004578, http://purl.obolibrary.org/obo/GO_0033273 GCST007366 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Blood protein levels up to 1,209 European ancestry individuals NA Illumina [up to 10879115] (imputed) 15 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST009159 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Homocysteine levels 1,208 European ancestry individuals NA Illumina [up to 10879115] (imputed) 1 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST009171 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Carotenoid levels up to 1,200 European ancestry individuals NA Illumina [up to 10879115] (imputed) 3 carotenoid measurement http://www.ebi.ac.uk/efo/EFO_0004737 GCST009160 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Diabetes biomarker traits up to 1,209 European ancestry individuals NA Illumina [up to 10879115] (imputed) 0 diabetes mellitus biomarker http://www.ebi.ac.uk/efo/EFO_0006842 GCST009161 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Hematology traits up to 1,209 European ancestry individuals NA Illumina [up to 10879115] (imputed) 0 hematological measurement http://www.ebi.ac.uk/efo/EFO_0004503 GCST009162 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Hormone measurements up to 1,200 European ancestry individuals NA Illumina [up to 10879115] (imputed) 3 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST009163 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Circulating inorganic ion levels up to 1,209 European ancestry individuals NA Illumina [up to 10879115] (imputed) 0 inorganic ion measurement http://www.ebi.ac.uk/efo/EFO_0010243 GCST009164 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Lipid or lipoprotein levels up to 1,206 European ancestry individuals NA Illumina [up to 10879115] (imputed) 6 lipid or lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0005105 GCST009165 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Renal system biomarkers up to 1,209 European ancestry individuals NA Illumina [up to 10879115] (imputed) 0 renal system measurement http://www.ebi.ac.uk/efo/EFO_0004742 GCST009166 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Vitamin levels up to 1,200 European ancestry individuals NA Illumina [up to 10879115] (imputed) 3 vitamin measurement http://www.ebi.ac.uk/efo/EFO_0004729 GCST009167 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Tumor necrosis factor alpha levels 1,167 European ancestry individuals 708 individuals Illumina [up to 10879115] (imputed) 0 tumor necrosis factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0004684 GCST009168 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Vitamin B12 levels 1,175 European ancestry individuals 2,083 individuals Illumina [up to 10879115] (imputed) 0 vitamin B12 measurement http://www.ebi.ac.uk/efo/EFO_0004620 GCST009169 Genome-wide genotyping array 2019-12-05 23696881 Wood AR 2013-05-16 PLoS One www.ncbi.nlm.nih.gov/pubmed/23696881 Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation. Chloride levels 1,206 European ancestry individuals 4,068 individuals Illumina [up to 10879115] (imputed) 0 chloride measurement http://www.ebi.ac.uk/efo/EFO_0009284 GCST009170 Genome-wide genotyping array 2019-04-15 30339177 Shane B 2018-10-19 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/30339177 The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. Red blood cell folate levels 2,232 Irish ancestry individuals NA Illumina [758443] 2 red blood cell folate measurement http://www.ebi.ac.uk/efo/EFO_0009703 GCST007580 Genome-wide genotyping array 2019-04-15 30339177 Shane B 2018-10-19 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/30339177 The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. Serum folate levels 2,232 Irish ancestry individuals NA Illumina [758443] 2 folic acid measurement http://www.ebi.ac.uk/efo/EFO_0005111 GCST007579 Genome-wide genotyping array 2019-04-15 30339177 Shane B 2018-10-19 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/30339177 The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. Plasma homocysteine levels 2,232 Irish ancestry individuals NA Illumina [758443] 5 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST007578 Genome-wide genotyping array 2019-04-04 28700999 Yang CK 2017-07-13 Cell Physiol Biochem www.ncbi.nlm.nih.gov/pubmed/28700999 Genome-Wide Association Study of MKI67 Expression and its Clinical Implications in HBV-Related Hepatocellular Carcinoma in Southern China. Hepatitis B virus-related hepatocellular carcinoma 195 Han Chinese ancestry cases 97 Han Chinese ancestry cases Illumina [242901] 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST007514 Targeted genotyping array [Exome array] 2020-02-19 31841498 Kampe A 2019-12-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31841498 Genetic variation in GC and CYP2R1 affects 25-hydroxyvitamin D concentration and skeletal parameters: A genome-wide association study in 24-month-old Finnish children. Serum 25-Hydroxyvitamin D levels 761 Finnish ancestry infants NA Illumina [5072729] (imputed) 2 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST009671 Genome-wide genotyping array 2021-07-07 33119750 Vergara C 2020-10-29 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33119750 A multi-ancestry sex stratified genome-wide association study of spontaneous clearance of hepatitis C virus. Hepatitis C (spontaneous viral clearance) 239 African ancestry male cases, 1,184 African ancestry male controls, 206 African ancestry female cases, 572 African ancestry female controls, 489 European ancestry male cases, 703 European ancestry male controls, 212 European ancestry female cases, 332 European ancestry female controls, 91 Hispanic male cases, 197 Hispanic male controls, 82 Hispanic female cases, 116 Hispanic female controls NA Illumina [5730693] (imputed) 14 remission, hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0009785, http://www.ebi.ac.uk/efo/EFO_0003047 GCST011999 Genome-wide genotyping array 2018-10-19 30181555 Strawbridge RJ 2018-09-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30181555 Genetics of self-reported risk-taking behaviour, trans-ethnic consistency and relevance to brain gene expression. Self-reported risk-taking behaviour 83,677 British ancestry cases, 244,662 British ancestry controls 2,764 South Asian ancestry cases, 3,139 African Caribbean ancestry cases, 16,169 European ancestry cases, 3,866 mixed ancestry cases, 4,267 South Asian ancestry controls, 4,341 African Caribbean ancestry controls, 31,814 European ancestry controls, 5,988 mixed ancestry controls Affymetrix [NR] (imputed) 25 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST006461 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia in non-obese individuals 8,363 European ancestry women NA NR [18717781] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007769 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia in higher physical activity 4,976 European ancestry women NA NR [18717781] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007770 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia in lower physical activity 6,818 European ancestry women NA NR [18717781] (imputed) 2 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007771 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia in more-fat diet 10,707 European ancestry women NA NR [18717781] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007772 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia in less-fat diet 1,087 European ancestry women NA NR [18717781] (imputed) 1 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007773 Genome-wide genotyping array 2018-11-01 30185882 Zeiger AM 2018-09-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30185882 Genetic Determinants of Telomere Length in African American Youth. Telomere length 492 African American children and adolescents NA Affymetrix [7519176] (imputed) 15 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST006485 Genome-wide genotyping array 2019-03-15 30706531 Tao F 2019-01-31 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/30706531 Variation in SIPA1L2 is Correlated with Phenotype Modification in CMT Type 1A. Reduced foot dorsiflexion strength in Charcot-Marie-Tooth disease type 1A 183 European ancestry cases severe cases, 147 European ancestry mild cases 55 Asian ancestry severe cases, 25 Asian ancestry mild cases Illumina [633827] 4 foot muscle strength measurement http://www.ebi.ac.uk/efo/EFO_0009699 GCST007304 Genome-wide genotyping array 2020-02-19 31855235 McComish BJ 2019-12-19 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31855235 Association of Genetic Variation With Keratoconus. Keratoconus 522 European ancestry cases, 655 European ancestry controls 818 European ancestry cases, 3,858 European ancestry controls Illumina [6252612] (imputed) 3 keratoconus http://purl.obolibrary.org/obo/MONDO_0015486 GCST009677 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Nose wing breadth 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006497 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Nose length 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006499 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Nosetip height 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006500 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Nasal root breadth 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006501 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Nasal root height 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006502 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Eye length 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 1 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST006503 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Interorbital distance 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST006504 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Labial fissure length 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST006505 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Lip thickness 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST006506 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Lower face length 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST006507 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Brow ridge morphology (principal component model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST006498 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Eye morphology (principal component model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST006508 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Side of face morphology (principal component model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST006509 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Cheek morphology (principal component model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST006510 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Nose morphology (principal component model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006511 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Mouth morphology (principal component model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 1 mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007955 GCST006512 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Brow ridge morphology (partial least square model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST006513 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Eye morphology (partial least square model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST006514 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Side of face morphology (partial least square model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST006515 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Cheek morphology (partial least square model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 1 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST006516 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Nose morphology (partial least square model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST006517 Genome-wide genotyping array 2018-11-06 30174134 Qiao L 2018-08-16 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/30174134 Genome-wide variants of Eurasian facial shape differentiation and a prospective model of DNA based face prediction. Mouth morphology (partial least square model) 424 Uyghur ancestry female individuals, 270 Uyghur ancestry male individuals 108 Uyghur ancestry female individuals, 63 Uyghur ancestry male individuals, 1,080 Han Chinese ancestry female individuals, 424 Han Chinese ancestry male individuals Illumina [8100752] (imputed) 0 mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007955 GCST006518 Genome-wide genotyping array 2021-04-16 33608531 Wu Y 2021-02-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33608531 GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression. Peptic ulcer disease 16,666 European ancestry cases, 439,661 European ancestry controls NA NR [8546065] (imputed) 8 peptic ulcer disease http://purl.obolibrary.org/obo/MONDO_0004247 GCST011504 Genome-wide genotyping array 2021-04-16 33608531 Wu Y 2021-02-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33608531 GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression. Gastroesophageal reflux disease 54,854 European ancestry cases, 401,473 European ancestry controls NA NR [8546065] (imputed) 6 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST011503 Genome-wide genotyping array 2021-04-16 33608531 Wu Y 2021-02-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33608531 GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression. Irritable bowel syndrome 28,518 European ancestry cases, 426,803 European ancestry controls NA NR [8546065] (imputed) 2 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST011502 Genome-wide genotyping array 2021-04-16 33608531 Wu Y 2021-02-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33608531 GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression. Inflammatory bowel disease 7,045 European ancestry cases, 449,282 European ancestry controls NA NR [8546065] (imputed) 31 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST011501 Genome-wide genotyping array 2021-04-16 33608531 Wu Y 2021-02-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33608531 GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression. Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment 90,175 European ancestry cases, 366,152 European ancestry controls NA NR [8546065] (imputed) 19 peptic ulcer disease, Peptic ulcer and gastro-oesophageal reflux disease (GORD) drug use measurement, gastroesophageal reflux disease http://purl.obolibrary.org/obo/MONDO_0004247, http://www.ebi.ac.uk/efo/EFO_0009923, http://www.ebi.ac.uk/efo/EFO_0003948 GCST011500 Genome-wide genotyping array 2020-02-19 31852448 Chiang KM 2019-12-18 BMC Genet www.ncbi.nlm.nih.gov/pubmed/31852448 Genome-wide association study of morbid obesity in Han Chinese. Obesity (extreme) 575 Han Chinese ancestry cases, 1,707 Han Chinese ancestry controls 535 Han Chinese ancestry cases, 9,145 Han Chinese ancestry controls Affymetrix [562523] 2 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST009673 Genome-wide genotyping array 2019-05-01 30852652 Schlicht K 2019-03-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30852652 The metabolic network coherence of human transcriptomes is associated with genetic variation at the cadherin 18 locus. Metabolic coherence (transcriptomic) 369 European ancestry individuals 3,783 European ancestry individuals Illumina [1067702] 1 metabolic network measurement, transcriptome measurement http://www.ebi.ac.uk/efo/EFO_0009864, http://www.ebi.ac.uk/efo/EFO_0009865 GCST007690 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure (long-term average) 5,304 African American individuals 6,500 African American individuals Affymetrix, Illumina [NR] (imputed) 9 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011905 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure (baseline) 5,304 African American individuals 6,500 African American individuals Affymetrix, Illumina [NR] (imputed) 26 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011902 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure change trajectory 5,304 African American individuals 6,500 African American individuals Affymetrix, Illumina [NR] (imputed) 6 diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006945 GCST011904 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure (long-term average) 5,304 African American individuals 6,500 African American individuals Affymetrix, Illumina [NR] (imputed) 19 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011903 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure change trajectory 5,304 African American individuals 6,500 African American individuals Affymetrix, Illumina [NR] (imputed) 9 systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006944 GCST011901 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure (long-term average) 13,137 European ancestry individuals 2,451 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 13 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011899 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure (baseline) 13,137 European ancestry individuals 2,451 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 12 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011900 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure change trajectory 13,137 European ancestry individuals 2,451 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 4 diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006945 GCST011898 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure (baseline) 13,137 European ancestry individuals 2,451 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011897 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure change trajectory 13,137 European ancestry individuals 2,451 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 4 systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006944 GCST011896 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure (long-term average) 5,304 African American individuals, 13,137 European ancestry individuals, 1,317 Hispanic individuals, 1,439 admixed individuals, 703 Chinese ancestry individuals 6,500 African American individuals, 2,451 European ancestry individuals, 2,869 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 20 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011895 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure (baseline) 5,304 African American individuals, 13,137 European ancestry individuals, 1,317 Hispanic individuals, 1,439 admixed individuals, 703 Chinese ancestry individuals 6,500 African American individuals, 2,451 European ancestry individuals, 2,869 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 15 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011894 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Diastolic blood pressure change trajectory 5,304 African American individuals, 13,137 European ancestry individuals, 1,317 Hispanic individuals, 1,439 admixed individuals, 703 Chinese ancestry individuals 6,500 African American individuals, 2,451 European ancestry individuals, 2,869 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 19 diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006945 GCST011893 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure (long-term average) 5,304 African American individuals, 13,137 European ancestry individuals, 1,317 Hispanic individuals, 1,439 admixed individuals, 703 Chinese ancestry individuals 6,500 African American individuals, 2,451 European ancestry individuals, 2,869 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 28 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011892 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure (baseline) 5,304 African American individuals, 13,137 European ancestry individuals, 1,317 Hispanic individuals, 1,439 admixed individuals, 703 Chinese ancestry individuals 6,500 African American individuals, 2,451 European ancestry individuals, 2,869 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 22 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011891 Genome-wide genotyping array 2021-06-15 33603002 Gouveia MH 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33603002 Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits. Systolic blood pressure change trajectory 5,304 African American individuals, 13,137 European ancestry individuals, 1,317 Hispanic individuals, 1,439 admixed individuals, 703 Chinese ancestry individuals 6,500 African American individuals, 2,451 European ancestry individuals, 2,869 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 8 systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006944 GCST011890 Genome-wide genotyping array 2021-08-05 33607172 Nygaard M 2021-02-16 Mech Ageing Dev www.ncbi.nlm.nih.gov/pubmed/33607172 Genome-wide association analysis of cognitive function in Danish long-lived individuals. Cognitive function in longevity 490 Danish ancestry individuals NA Illumina [4827900] (imputed) 14 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012170 Genome-wide genotyping array 2019-06-26 28714974 Klarin D 2017-07-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28714974 Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease. Coronary artery disease 4,831 European ancestry cases, 115,455 European ancestry controls up to 60,801 European and unknown ancestry cases, up to 123,504 European and unknown ancestry controls Affymetrix [9061845] (imputed) 20 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST007990 Genome-wide genotyping array 2019-04-25 30837465 Wittemans LBL 2019-03-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30837465 Assessing the causal association of glycine with risk of cardio-metabolic diseases. Glycine levels 80,003 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 50 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST007638 Genome-wide genotyping array 2019-07-29 28585551 Sigurdsson S 2017-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28585551 Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis. Diverticular disease 5,426 Icelandic ancestry cases, 245,951 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) 5,970 Danish ancestry cases, 3,020 Danish ancestry controls Illumina [32463443] (imputed) 4 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST008257 Genome-wide genotyping array, Genome-wide sequencing 2019-07-29 28585551 Sigurdsson S 2017-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28585551 Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis. Diverticulitis 2,764 Icelandic ancestry cases, 245,951 Icelandic ancestry controls (includes non-array genotyped, whole-genome imputed individuals) NA Illumina [32463443] (imputed) 10 diverticulitis http://www.ebi.ac.uk/efo/EFO_1001460 GCST008256 Genome-wide genotyping array, Genome-wide sequencing 2021-04-14 33321069 van Zuydam NR 2020-08-13 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33321069 Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus. Coronary artery disease in type 2 diabetes 5,864 European ancestry cases, 4,150 South Asian ancestry cases, 11,655 European ancestry controls, 2,590 South Asian ancestry controls 3,706 European ancestry cases, 7,831 European ancestry controls Affymetrix, Illumina [at least 119674] (imputed) 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST011490 Genome-wide genotyping array 2021-04-14 33321069 van Zuydam NR 2020-08-13 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33321069 Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus. Coronary artery disease in individuals without type 2 diabetes 13,381 European ancestry cases, 4,313 South Asian ancestry cases, 18,926 European ancestry controls, 5,764 South Asian ancestry controls 12,988 European ancestry cases, 93,252 European ancestry controls Affymetrix, Illumina [at least 119674] (imputed) 2 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST011489 Genome-wide genotyping array 2021-04-14 33321069 van Zuydam NR 2020-08-13 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33321069 Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus. Coronary artery disease 19,245 European ancestry cases, 8,463 South Asian ancestry cases, 30,581 European ancestry controls, 8,354 South Asian ancestry controls 16,704 European ancestry cases, 101,083 European ancestry controls Affymetrix, Illumina [at least 119674] (imputed) 8 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST011488 Genome-wide genotyping array 2021-04-14 33321069 van Zuydam NR 2020-08-13 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33321069 Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus. Coronary artery disease x type 2 diabetes interaction 10,014 European and South Asian ancestry cases with type 2 diabetes, 17,694 European and South Asian ancestry cases without type 2 diabetes, 14,245 European and South Asian ancestry controls with type 2 diabetes, 24,690 European and South Asian ancestry controls without type 2 diabetes 3,706 European ancestry cases with type 2 diabetes, 12,988 European ancestry cases without type 2 diabetes, 7,831 European ancestry controls with type 2 diabetes, 93,252 European ancestry controls without type 2 diabetes Affymetrix, Illumina [at least 119674] (imputed) 0 type 2 diabetes mellitus, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011487 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Sensation seeking 22,745 European ancestry individuals NA Illumina [11434023] (imputed) 5 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007621 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Impulsivity 21,495 European ancestry individuals NA Illumina [11508759] (imputed) 5 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007622 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Lack of premeditation 22,774 European ancestry individuals NA Illumina [11455628] (imputed) 5 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007623 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Positive urgency 22,738 European ancestry individuals NA Illumina [11434023] (imputed) 6 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007624 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Negative urgency 22,795 European ancestry individuals NA Illumina [11434023] (imputed) 5 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007625 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Lack of perseverance 22,861 European ancestry individuals NA Illumina [11914280] (imputed) 6 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007626 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Impulsivity (attentional) 21,876 European ancestry individuals NA Illumina [11455070] (imputed) 5 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007627 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Impulsivity (motor) 21,806 European ancestry individuals NA Illumina [11434023] (imputed) 5 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007628 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Impulsivity (non-planning) 21,786 European ancestry individuals NA Illumina [11434023] (imputed) 5 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST007629 Genome-wide genotyping array 2019-04-24 30718321 Sanchez-Roige S 2019-02-04 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30718321 Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes. Drug experimentation measurement 22,572 European ancestry individuals NA Illumina [11434023] (imputed) 5 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST007630 Genome-wide genotyping array 2021-07-27 33469137 Crawford AA 2021-01-20 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33469137 Variation in the SERPINA6/SERPINA1 locus alters morning plasma cortisol, hepatic corticosteroid binding globulin expression, gene expression in peripheral tissues, and risk of cardiovascular disease. Plasma cortisol levels (morning) 25,314 European ancestry individuals NA Affymetrix, Illumina [8452427] (imputed) 4 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST012087 Genome-wide genotyping array 2021-02-26 33477890 Voorhies K 2021-01-19 J Pers Med www.ncbi.nlm.nih.gov/pubmed/33477890 Age by Single Nucleotide Polymorphism Interactions on Bronchodilator Response in Asthmatics. Bronchodilator response x age interaction in asthma 892 European ancestry individuals 559 European ancestry individuals NR [5638778] (imputed) 0 response to bronchodilator, age at assessment http://purl.obolibrary.org/obo/GO_0097366, http://www.ebi.ac.uk/efo/EFO_0008007 GCST011164 Genome-wide genotyping array 2018-10-31 30177863 Maguire LH 2018-09-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30177863 Genome-wide association analyses identify 39 new susceptibility loci for diverticular disease. Diverticular disease 27,444 British ancestry cases, 382,284 British ancestry controls NA Affymetrix [> 30000000] (imputed) 153 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST006479 Genome-wide genotyping array 2020-06-26 31837886 Kennedy OJ 2019-12-02 Am J Kidney Dis www.ncbi.nlm.nih.gov/pubmed/31837886 Coffee Consumption and Kidney Function: A Mendelian Randomization Study. Coffee consumption (cups per day) 227,666 British ancestry individuals NA NR [NR] 25 cups of coffee per day measurement http://www.ebi.ac.uk/efo/EFO_0006782 GCST010108 Genome-wide genotyping array 2021-03-18 31846791 Kim HJ 2019-12-09 Chemosphere www.ncbi.nlm.nih.gov/pubmed/31846791 A genome-wide by PM10 interaction study identifies novel loci for lung function near BICD1 and IL1RN-IL1F10 genes in Korean adults. Lung function x fine particulate matter exposure levels interaction 1,826 Korean ancestry individuals 892 Korean ancestry individuals Illumina [197275] 0 pulmonary function measurement, particulate matter air pollution measurement http://www.ebi.ac.uk/efo/EFO_0003892, http://www.ebi.ac.uk/efo/EFO_0008255 GCST011299 Genome-wide genotyping array 2019-04-12 30846698 Dashti HS 2019-03-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30846698 Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. Sleep duration (short sleep) 106,192 European ancestry cases, 305,742 European ancestry controls 47,180 adults, 10,554 children or adolescents NR [14661600] (imputed) 27 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST007559 Genome-wide genotyping array 2019-04-12 30846698 Dashti HS 2019-03-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30846698 Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. Sleep duration (long sleep) 34,184 European ancestry cases, 305,742 European ancestry controls 47,180 adults, 10,554 children or adolescents Affymetrix [14661600] (imputed) 8 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST007560 Genome-wide genotyping array 2019-04-12 30846698 Dashti HS 2019-03-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30846698 Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. Sleep duration 446,118 European ancestry individuals 47,180 adults, 10,554 children or adolescents Affymetrix [14661600] (imputed) 72 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST007561 Genome-wide genotyping array 2019-03-02 30383316 Malik R 2018-11-01 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/30383316 Genome-Wide Meta-analysis identifies three novel loci associated with stroke. Ischemic stroke 37,845 European ancestry cases, 26,124 cases, 775,530 European ancestry controls, 48,339 controls NA NR [NR] 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST007249 Genome-wide genotyping array 2019-03-02 30383316 Malik R 2018-11-01 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/30383316 Genome-Wide Meta-analysis identifies three novel loci associated with stroke. Stroke 45,570 European ancestry cases, 26,577 cases, 775,530 European ancestry controls, 48,339 controls NA NR [NR] 3 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST007248 Genome-wide genotyping array 2019-06-21 31081985 Stein MB 2019-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/31081985 Genome-wide analyses of psychological resilience in U.S. Army soldiers. Psychological resilience (outcome-based) in high deployment stress exposure 581 European ancestry cases and controls NA Illumina [at least 664457] (imputed) 2 psychological resilience measurement http://www.ebi.ac.uk/efo/EFO_0009945 GCST007945 Genome-wide genotyping array 2019-06-21 31081985 Stein MB 2019-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/31081985 Genome-wide analyses of psychological resilience in U.S. Army soldiers. Psychological resilience (self-assessed) 11,473 European ancestry individuals NA Illumina [at least 360704] (imputed) 2 psychological resilience measurement http://www.ebi.ac.uk/efo/EFO_0009945 GCST007946 Genome-wide genotyping array 2019-06-21 31081985 Stein MB 2019-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/31081985 Genome-wide analyses of psychological resilience in U.S. Army soldiers. Psychological resilience (outcome-based) 1,558 European ancestry resilient cases, 381 European ancestry controls with post-deployment mental disorder NA Illumina [at least 664457] (imputed) 5 psychological resilience measurement http://www.ebi.ac.uk/efo/EFO_0009945 GCST007947 Genome-wide genotyping array 2018-12-06 30319691 Liu C 2018-09-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/30319691 Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development. Cerebrospinal fluid AB1-42 levels 235 early mild cognitive impairment cases, 249 late mild cognitive impairment cases, 47 Alzheimer's disease cases, 281 controls. NA Illumina [575353] 14 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST006672 Genome-wide genotyping array 2018-12-06 30319691 Liu C 2018-09-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/30319691 Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development. Cerebrospinal fluid t-tau:AB1-42 ratio 235 early mild cognitive impairment cases, 249 late mild cognitive impairment cases, 47 Alzheimer's disease cases, 281 controls. NA Illumina [575353] 14 t-tau:beta-amyloid 1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0007708 GCST006673 Genome-wide genotyping array 2018-12-06 30319691 Liu C 2018-09-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/30319691 Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development. Cerebrospinal fluid p-Tau181p:AB1-42 ratio 235 early mild cognitive impairment cases, 249 late mild cognitive impairment cases, 47 Alzheimer's disease cases, 281 controls. NA Illumina [575353] 14 p-tau:beta-amyloid 1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0007709 GCST006674 Genome-wide genotyping array 2018-12-06 30319691 Liu C 2018-09-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/30319691 Genome-Wide Association and Mechanistic Studies Indicate That Immune Response Contributes to Alzheimer's Disease Development. Cognitive impairment test score 235 early mild cognitive impairment cases, 249 late mild cognitive impairment cases, 47 Alzheimer's disease cases, 281 controls. NA Illumina [575353] 20 cognitive impairment measurement http://www.ebi.ac.uk/efo/EFO_0007998 GCST006671 Genome-wide genotyping array 2019-02-20 30284742 Bevilacqua L 2018-10-04 J Periodontal Res www.ncbi.nlm.nih.gov/pubmed/30284742 A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population. Chronic periodontitis 442 Friuli Venezia Giulia (founder/genetic isolate) cases, 160 Friuli Venezia Giulia (founder/genetic isolate) controls NA Illumina [NR] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST007196 Genome-wide genotyping array 2019-02-20 30284742 Bevilacqua L 2018-10-04 J Periodontal Res www.ncbi.nlm.nih.gov/pubmed/30284742 A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population. Chronic periodontitis (slight) 273 Friuli Venezia Giulia (founder/genetic isolate) cases, 160 Friuli Venezia Giulia (founder/genetic isolate) controls NA Illumina [NR] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST007195 Genome-wide genotyping array 2019-02-20 30284742 Bevilacqua L 2018-10-04 J Periodontal Res www.ncbi.nlm.nih.gov/pubmed/30284742 A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population. Chronic periodontitis (severe) 169 Friuli Venezia Giulia (founder/genetic isolate) cases, 160 Friuli Venezia Giulia (founder/genetic isolate) controls NA Illumina [NR] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST007194 Genome-wide genotyping array 2019-02-20 30284742 Bevilacqua L 2018-10-04 J Periodontal Res www.ncbi.nlm.nih.gov/pubmed/30284742 A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population. Chronic periodontitis (generalised) 235 Friuli Venezia Giulia (founder/genetic isolate) cases, 160 Friuli Venezia Giulia (founder/genetic isolate) controls NA Illumina [NR] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST007193 Genome-wide genotyping array 2019-02-20 30284742 Bevilacqua L 2018-10-04 J Periodontal Res www.ncbi.nlm.nih.gov/pubmed/30284742 A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population. Chronic periodontitis (localised) 207 Friuli Venezia Giulia (founder/genetic isolate) cases, 160 Friuli Venezia Giulia (founder/genetic isolate) controls NA Illumina [NR] (imputed) 1 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST007197 Genome-wide genotyping array 2019-02-28 30287865 Pinar A 2018-10-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30287865 Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time. Intra-individual response time variability (response selection) 857 European ancestry individuals NA Illumina [5408162] (imputed) 0 intra-individual reaction time variability measurement http://www.ebi.ac.uk/efo/EFO_0009702 GCST007244 Genome-wide genotyping array 2019-02-28 30287865 Pinar A 2018-10-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30287865 Genome-wide association study reveals novel genetic locus associated with intra-individual variability in response time. Intra-individual response time variability (selective attention) 857 European ancestry individuals NA Illumina [5408162] (imputed) 2 intra-individual reaction time variability measurement http://www.ebi.ac.uk/efo/EFO_0009702 GCST007243 Genome-wide genotyping array 2021-07-27 33483693 Clements CC 2021-01-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/33483693 Genome-wide association study of patients with a severe major depressive episode treated with electroconvulsive therapy. Major depressive episode treated with electroconvulsive therapy 2,725 European ancestry cases, 3,290 European ancestry controls NA Illumina [NR] (imputed) 30 major depressive episode http://www.ebi.ac.uk/efo/EFO_0007634 GCST012095 Genome-wide genotyping array 2021-07-27 33483693 Clements CC 2021-01-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/33483693 Genome-wide association study of patients with a severe major depressive episode treated with electroconvulsive therapy. Major depressive disorder and major depressive episode treated with electroconvulsive therapy 1,796 European ancestry cases, 3,290 European ancestry controls NA Illumina [NR] (imputed) 22 major depressive episode, major depressive disorder http://www.ebi.ac.uk/efo/EFO_0007634, http://purl.obolibrary.org/obo/MONDO_0002009 GCST012094 Genome-wide genotyping array 2019-04-16 30833571 Wiberg A 2019-03-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30833571 A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. Carpal tunnel syndrome 12,312 European ancestry cases, 389,344 European ancestry controls NA Affymetrix [84000000] (imputed) 16 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST007581 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia 11,794 European ancestry women NA NR [18717781] (imputed) 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007744 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia in obesity 3,431 European ancestry women NA NR [18717781] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007745 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia in non-obese individuals 8,363 European ancestry women NA NR [18717781] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007746 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia in lower physical activity 6,818 European ancestry women NA NR [18717781] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007747 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia in higher physical activity 4,976 European ancestry women NA NR [18717781] (imputed) 2 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007748 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia in more-fat diet 10,707 European ancestry women NA NR [18717781] (imputed) 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007749 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia in less-fat diet 1,087 European ancestry women NA NR [18717781] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007750 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance in obesity 3,431 European ancestry women NA NR [18717781] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST007751 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance in non-obese individuals 8,363 European ancestry women NA NR [18717781] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST007752 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance in higher physical activity 4,976 European ancestry women NA NR [18717781] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST007753 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance in lower physical activity 6,818 European ancestry women NA NR [18717781] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST007754 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance in more-fat diet 10,707 European ancestry women NA NR [18717781] (imputed) 2 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST007755 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance in less-fat diet 1,087 European ancestry women NA NR [18717781] (imputed) 2 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST007756 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia x BMI interaction 8,363 European ancestry non-obese women, 3,431 European ancestry obese women NA NR [18717781] (imputed) 0 body mass index, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004465 GCST007757 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia x physical activity interaction 4,976 European ancestry active women, 6,818 European ancestry inactive women NA NR [18717781] (imputed) 0 physical activity measurement, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004465 GCST007758 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperglycemia x saturated fatty acids interaction 1,087 European ancestry less-fat diet women, 10,707 European ancestry more-fat diet women NA NR [18717781] (imputed) 0 fatty acid measurement, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004465 GCST007759 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia 11,794 European ancestry women NA NR [18717781] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007760 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance 11,794 European ancestry women NA NR [18717781] (imputed) 2 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST007761 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia x BMI interaction 8,363 European ancestry non-obese women, 3,431 European ancestry obese women NA NR [18717781] (imputed) 1 body mass index, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004466 GCST007762 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance x BMI interaction 8,363 European ancestry non-obese women, 3,431 European ancestry obese women NA NR [18717781] (imputed) 0 insulin resistance, body mass index http://www.ebi.ac.uk/efo/EFO_0002614, http://www.ebi.ac.uk/efo/EFO_0004340 GCST007763 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia x physical activity interaction 4,976 European ancestry active women, 6,818 European ancestry inactive women NA NR [18717781] (imputed) 1 physical activity measurement, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004466 GCST007764 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance x physical activity interaction 4,976 European ancestry active women, 6,818 European ancestry inactive women NA NR [18717781] (imputed) 0 insulin resistance, physical activity measurement http://www.ebi.ac.uk/efo/EFO_0002614, http://www.ebi.ac.uk/efo/EFO_0008002 GCST007765 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia x saturated fatty acids interaction 1,087 European ancestry less-fat diet women, 10,707 European ancestry more-fat diet women NA NR [18717781] (imputed) 1 fatty acid measurement, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0004466 GCST007766 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Homeostasis model assessment of insulin resistance x saturated fatty acids interaction 1,087 European ancestry less-fat diet women, 10,707 European ancestry more-fat diet women NA NR [18717781] (imputed) 1 fatty acid measurement, insulin resistance http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0002614 GCST007767 Genome-wide genotyping array 2019-05-09 30327367 Jung SY 2018-10-16 Cancer Prev Res (Phila) www.ncbi.nlm.nih.gov/pubmed/30327367 Genome-wide meta-analysis of gene-environmental interaction for insulin-resistance phenotypes and breast cancer risk in postmenopausal women. Hyperinsulinemia in obesity 3,431 European ancestry women NA NR [18717781] (imputed) 1 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007768 Genome-wide genotyping array 2018-10-17 30178632 Meng W 2018-09-04 Acta Ophthalmol www.ncbi.nlm.nih.gov/pubmed/30178632 A genome-wide association study suggests new evidence for an association of the NADPH Oxidase 4 (NOX4) gene with severe diabetic retinopathy in type 2 diabetes. Severe diabetic retinopathy in type 2 diabetes 560 Scottish ancestry proliferative or severe background retinopathy cases, 4,106 Scottish ancestry mild or no retinopathy controls NA Affymetrix, Illumina [6585471] (imputed) 2 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST006424 Genome-wide genotyping array 2019-02-08 30194254 Sud A 2018-09-07 Blood www.ncbi.nlm.nih.gov/pubmed/30194254 Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma. Hodgkin's lymphoma 5,325 European ancestry cases, 22,425 European ancestry controls NA Illumina [> 10000000] (imputed) 6 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST007062 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or body mass index (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 339,224 European and unknown ancestry individuals with body mass index measurements NA NR [2590752] 0 body mass index, birth weight http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008773 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or waist-hip ratio (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 224,459 European and unknown ancestry individuals with waist-hip ratio measurements NA NR [2566817] 0 waist-hip ratio, birth weight http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008774 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or waist circumference (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 224,459 European and unknown ancestry individuals with waist circumference measurements NA NR [2569939] 0 waist circumference, birth weight http://www.ebi.ac.uk/efo/EFO_0004342, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008775 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or type 2 diabetes (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 110,452 European and unknown ancestry individuals with type 2 diabetes data NA NR [2893797] 0 birth weight, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0004344, http://purl.obolibrary.org/obo/MONDO_0005148 GCST008776 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or fasting glucose levels (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 46,186 European and unknown ancestry individuals with fasting glucose measurements NA NR [2495051] 0 birth weight, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0004465 GCST008777 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or fasting insulin levels (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 46,186 European and unknown ancestry individuals with fasting insulin measurements NA NR [2495051] 0 birth weight, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0004466 GCST008778 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or hemoglobin A1C levels (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 46,368 European and unknown ancestry individuals with hemoglobin A1C measurements NA NR [2566561] 0 HbA1c measurement, birth weight http://www.ebi.ac.uk/efo/EFO_0004541, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008779 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or insulin secretion (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 5,318 European and unknown ancestry individuals with insulin secretion measurements NA NR [2460930] 0 insulin secretion measurement, birth weight http://www.ebi.ac.uk/efo/EFO_0008001, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008780 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or insulin sensitivity index (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 16,753 European and unknown ancestry individuals with insulin sensitivity measurements NA NR [2459303] 0 insulin sensitivity measurement, birth weight http://www.ebi.ac.uk/efo/EFO_0004471, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008781 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or coronary artery disease (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 184,305 European and unknown ancestry individuals with coronary artery disease data NA NR [8544005] 0 birth weight, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0001645 GCST008782 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or myocardial infarction (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 129,000 European and unknown ancestry individuals with myocardial infarction data NA NR [8541959] 0 birth weight, myocardial infarction http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0000612 GCST008783 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or LDL cholesterol levels (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 188,577 European and unknown ancestry individuals with LDL cholesterol measurements NA NR [2471777] 0 low density lipoprotein cholesterol measurement, birth weight http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008784 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or HDL cholesterol levels (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 188,577 European and unknown ancestry individuals with HDL cholesterol measurements NA NR [2481375] 0 birth weight, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0004612 GCST008785 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or total cholesterol levels (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 188,577 European and unknown ancestry individuals with total cholesterol measurements NA NR [2480907] 0 total cholesterol measurement, birth weight http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008786 Genome-wide genotyping array 2019-09-30 30858448 Tekola-Ayele F 2019-03-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30858448 Genetic overlap between birthweight and adult cardiometabolic diseases has implications for genomic medicine. Birth weight or triglycerides levels (pleiotropy) 153,781 European and unknown ancestry individuals with birth weight measurements, 188,577 European and unknown ancestry individuals with triglycerides measurements NA NR [2473236] 0 triglyceride measurement, birth weight http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004344 GCST008787 Genome-wide genotyping array 2021-08-04 33589587 Sakaue S 2021-02-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33589587 Genetic determinants of risk in autoimmune pulmonary alveolar proteinosis. Autoimmune pulmonary alveolar proteinosis 198 Japanese ancestry cases, 395 Japanese ancestry controls NA Illumina [12153232] (imputed) 2 pulmonary alveolar proteinosis http://purl.obolibrary.org/obo/MONDO_0001437 GCST012169 Genome-wide genotyping array 2019-10-31 29593015 Montasser ME 2018-09-01 Circulation www.ncbi.nlm.nih.gov/pubmed/29593015 An APOO Pseudogene on Chromosome 5q Is Associated With Low-Density Lipoprotein Cholesterol Levels. Low density lipoprotein cholesterol levels 1,102 Old Order Amish (founder/genetic isolate) individuals 798 Old Order Amish (founder/genetic isolate) individuals Illumina [124907] 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST008990 Targeted genotyping array [Cardio-Metabochip] 2021-05-14 32846279 Zheng Q 2020-06-29 Sleep Med www.ncbi.nlm.nih.gov/pubmed/32846279 Identification of genetic loci jointly influencing coronary artery disease risk and sleep traits of insomnia, sleep duration, and chronotype. Coronary artery disease and insomnia (pleiotropy) 60,801 European, South Asian, East Asian, Hispanic and African American ancestry coronary artery disease cases, 109,402 European ancestry insomnia cases, 400,635 European, South Asian, East Asian, Hispanic and African American ancestry controls NA Affymetrix [up to 10848137] (imputed) 0 insomnia, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004698, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011660 Genome-wide genotyping array 2021-05-14 32846279 Zheng Q 2020-06-29 Sleep Med www.ncbi.nlm.nih.gov/pubmed/32846279 Identification of genetic loci jointly influencing coronary artery disease risk and sleep traits of insomnia, sleep duration, and chronotype. Coronary artery disease and sleep duration (pleiotropy) 60,801 European, South Asian, East Asian, Hispanic and African American ancestry coronary artery disease cases, 384,317 European ancestry individuals with sleep duration measurements, 123,504 European, South Asian, East Asian, Hispanic and African American ancestry controls NA Affymetrix [up to 10848137] (imputed) 0 sleep duration, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0005271, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011659 Genome-wide genotyping array 2021-05-14 32846279 Zheng Q 2020-06-29 Sleep Med www.ncbi.nlm.nih.gov/pubmed/32846279 Identification of genetic loci jointly influencing coronary artery disease risk and sleep traits of insomnia, sleep duration, and chronotype. Coronary artery disease and chronotype (pleiotropy) 60,801 European, South Asian, East Asian, Hispanic and African American ancestry coronary artery disease cases, 345,552 European ancestry individuals with chronotype measurement, 123,504 European, South Asian, East Asian, Hispanic and African American ancestry controls NA Affymetrix [up to 10848137] (imputed) 0 chronotype measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0008328, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011658 Genome-wide genotyping array 2018-11-05 30247649 Gonzalez-Serna D 2018-09-21 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/30247649 Analysis of the genetic component of systemic sclerosis in Iranian and Turkish populations through a genome-wide association study. Systemic sclerosis 764 Middle Eastern ancestry cases, 1,343 Middle Eastern ancestry controls NA Illumina [5698748] (imputed) 11 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST006493 Genome-wide genotyping array 2022-10-14 32840624 Kho M 2020-08-25 J Nutr www.ncbi.nlm.nih.gov/pubmed/32840624 Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples. Urinary sodium excretion 6,519 European ancestry individuals 844 European ancestry individuals, 1,246 African ancestry individuals, 2,475 Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST013024 Genome-wide genotyping array 2022-10-14 32840624 Kho M 2020-08-25 J Nutr www.ncbi.nlm.nih.gov/pubmed/32840624 Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples. Urinary potassium excretion 6,519 European ancestry individuals 844 European ancestry individuals, 1,246 African ancestry individuals, 2,475 Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 dietary potassium intake measurement http://www.ebi.ac.uk/efo/EFO_0008470 GCST013025 Genome-wide genotyping array 2022-10-14 32840624 Kho M 2020-08-25 J Nutr www.ncbi.nlm.nih.gov/pubmed/32840624 Genome-Wide Association Meta-Analysis of Individuals of European Ancestry Identifies Suggestive Loci for Sodium Intake, Potassium Intake, and Their Ratio Measured from 24-Hour or Half-Day Urine Samples. Urinary sodium to potassium ratio 6,519 European ancestry individuals 844 European ancestry individuals, 1,246 African ancestry individuals, 2,475 Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 urinary sodium to potassium ratio http://www.ebi.ac.uk/efo/EFO_0009884 GCST013026 Genome-wide genotyping array 2021-05-19 32913026 Knol MJ 2020-09-10 Neurology www.ncbi.nlm.nih.gov/pubmed/32913026 Association of common genetic variants with brain microbleeds: A Genome-wide Association Study. Cerebral microbleeds 3,321 European ancestry cases, 42 Chinese ancestry cases, 75 Malay ancestry cases, 118 African American cases, 21,785 European ancestry controls, 88 Chinese ancestry controls, 129 Malay ancestry controls, 304 African American controls NA Affymetrix, Illumina [NR] (imputed) 4 cerebral microbleeds http://www.ebi.ac.uk/efo/EFO_0010059 GCST011707 Genome-wide genotyping array 2021-05-19 32913026 Knol MJ 2020-09-10 Neurology www.ncbi.nlm.nih.gov/pubmed/32913026 Association of common genetic variants with brain microbleeds: A Genome-wide Association Study. Cerebral microbleeds (lobar) 2,035 European ancestry cases, 27 Chinese ancestry cases, 36 Malay ancestry cases, 81 African American cases, 21,785 European ancestry controls, 88 Chinese ancestry controls, 129 Malay ancestry controls, 304 African American controls NA Affymetrix, Illumina [NR] (imputed) 5 cerebral microbleeds http://www.ebi.ac.uk/efo/EFO_0010059 GCST011706 Genome-wide genotyping array 2021-05-19 32913026 Knol MJ 2020-09-10 Neurology www.ncbi.nlm.nih.gov/pubmed/32913026 Association of common genetic variants with brain microbleeds: A Genome-wide Association Study. Cerebral microbleeds (mixed) 1,262 European ancestry cases, 31 African American cases, 21,785 European ancestry controls, 88 Chinese ancestry controls, 129 Malay ancestry controls, 304 African American controls NA Affymetrix, Illumina [NR] (imputed) 0 cerebral microbleeds http://www.ebi.ac.uk/efo/EFO_0010059 GCST011708 Genome-wide genotyping array 2019-02-14 30258056 Vojinovic D 2018-09-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30258056 Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume. Lateral ventricular volume in normal aging 22,045 European ancestry individuals, 1,488 African American individuals NA Affymetrix, Illumina [NR] (imputed) 7 lateral ventricle volume measurement http://www.ebi.ac.uk/efo/EFO_0008487 GCST007147 Genome-wide genotyping array 2019-07-10 30661054 Schafmayer C 2019-01-19 Gut www.ncbi.nlm.nih.gov/pubmed/30661054 Genome-wide association analysis of diverticular disease points towards neuromuscular, connective tissue and epithelial pathomechanisms. Diverticular disease 31,964 European ancestry cases, 419,135 European ancestry controls 4,611 European ancestry cases, 31,478 European ancestry controls Affymetrix [11977111] (imputed) 3 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST008105 Genome-wide genotyping array 2019-06-21 30685440 Silbernagel G 2018-12-28 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/30685440 LDL triglycerides, hepatic lipase activity, and coronary artery disease: An epidemiologic and Mendelian randomization study. Low density lipoprotein triglyceride levels 2,900 German ancestry individuals NA Affymetrix [2543887] (imputed) 0 low density lipoprotein triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0009946 GCST007955 Genome-wide genotyping array 2019-01-28 29555444 Hamer MA 2018-03-16 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/29555444 Facial Wrinkles in Europeans: a Genome-Wide Association Study. Facial wrinkles 3,513 north-western European ancestry individuals 599 north-western European ancestry individuals Illumina [9009554] (imputed) 19 Facial wrinkling http://purl.obolibrary.org/obo/HP_0009762 GCST006981 Genome-wide genotyping array 2021-04-16 32895509 Suzuki T 2020-09-07 Eur J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/32895509 A genome-wide association study on fish consumption in a Japanese population-the Japan Multi-Institutional Collaborative Cohort study. Fish consumption 13,739 Japanese ancestry individuals 2,845 Japanese ancestry individuals Illumina [8504983] (imputed) 2 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST011499 Genome-wide genotyping array 2018-11-26 30166627 Massey J 2018-08-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30166627 Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis. Response to TNF inhibitor in rheumatoid arthritis (erythrocyte sedimentation rate) 487 European ancestry individuals treated with adalimumab, 549 European ancestry individuals treated with etanercept, 414 European ancestry individuals treated with infliximab, 64 European ancestry individuals treated with other TNF inhibitors NA Affymetrix, Illumina [9814288] (imputed) 1 response to TNF antagonist, blood sedimentation http://www.ebi.ac.uk/efo/EFO_0004653, http://www.ebi.ac.uk/efo/EFO_0004304 GCST006607 Genome-wide genotyping array 2018-11-26 30166627 Massey J 2018-08-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30166627 Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis. Response to TNF inhibitor in rheumatoid arthritis (change in swollen 28-joint count) 551 European ancestry individuals treated with adalimumab, 619 European ancestry individuals treated with etanercept, 434 European ancestry individuals treated with infliximab, 119 European ancestry individuals treated with other TNF inhibitors NA Affymetrix, Illumina [9814288] (imputed) 13 response to TNF antagonist, joint damage measurement http://www.ebi.ac.uk/efo/EFO_0004653, http://www.ebi.ac.uk/efo/EFO_0005413 GCST006606 Genome-wide genotyping array 2018-11-26 30166627 Massey J 2018-08-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30166627 Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis. Response to TNF inhibitor in rheumatoid arthritis (change in patient global heath assessment score) 549 European ancestry individuals treated with adalimumab, 615 European ancestry individuals treated with etanercept, 426 European ancestry individuals treated with infliximab, 119 European ancestry individuals treated with other TNF inhibitors NA Affymetrix, Illumina [9814288] (imputed) 1 self rated health, response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004778, http://www.ebi.ac.uk/efo/EFO_0004653 GCST006608 Genome-wide genotyping array 2018-11-26 30166627 Massey J 2018-08-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30166627 Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis. Response to TNF inhibitor in rheumatoid arthritis (change in tender 28-joint count) 551 European ancestry individuals treated with adalimumab, 619 European ancestry individuals treated with etanercept, 434 European ancestry individuals treated with infliximab, 119 European ancestry individuals treated with other TNF inhibitors NA Affymetrix, Illumina [9814288] (imputed) 7 response to TNF antagonist, joint damage measurement http://www.ebi.ac.uk/efo/EFO_0004653, http://www.ebi.ac.uk/efo/EFO_0005413 GCST006609 Genome-wide genotyping array 2018-11-26 30166627 Massey J 2018-08-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30166627 Genome-wide association study of response to tumour necrosis factor inhibitor therapy in rheumatoid arthritis. Response to TNF inhibitor in rheumatoid arthritis (change in disease activity score) 500 European ancestry individuals treated with adalimumab, 564 European ancestry individuals treated with etanercept, 441 European ancestry individuals treated with infliximab, 64 European ancestry individuals treated with other TNF inhibitors NA Affymetrix, Illumina [9814288] (imputed) 1 response to TNF antagonist, arthritis disease activity score measurement http://www.ebi.ac.uk/efo/EFO_0004653, http://www.ebi.ac.uk/efo/EFO_0009435 GCST006610 Genome-wide genotyping array 2018-11-30 30279531 Baselmans BML 2018-10-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30279531 A genetic perspective on the relationship between eudaimonic -and hedonic well-being. Eudaimonic well-being 108,154 British ancestry individuals NA Affymetrix [~ 8600000] (imputed) 21 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST006635 Genome-wide genotyping array 2018-11-30 30279531 Baselmans BML 2018-10-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30279531 A genetic perspective on the relationship between eudaimonic -and hedonic well-being. Hedonic well-being 221,575 British ancestry individuals NA Affymetrix [~ 8600000] (imputed) 6 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST006634 Genome-wide genotyping array 2019-02-12 30297428 Jorgenson E 2018-10-08 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/30297428 Genetic variation in the SIM1 locus is associated with erectile dysfunction. Erectile dysfunction 11,864 European ancestry cases, 1,016 Hispanic cases, 938 East Asian ancestry cases, 397 African American cases, 17,995 European ancestry controls, 1,954 Hispanic controls, 1,799 East Asian ancestry controls, 686 African American controls 2,783 European ancestry cases, 70 South Asian ancestry cases, 68 African British cases, 2 East Asian ancestry cases, 36 mixed and unknown ancestry cases, 206,975 European ancestry controls, 5,234 South Asian ancestry controls, 3,566 African British controls, 678 East Asian ancestry controls, 3,626 mixed and unknown ancestry controls Affymetrix [665000] 1 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST007118 Genome-wide genotyping array 2018-06-06 29728394 Blauw LL 2018-05-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/29728394 CETP (Cholesteryl Ester Transfer Protein) Concentration: A Genome-Wide Association Study Followed by Mendelian Randomization on Coronary Artery Disease. Cholesteryl ester transfer protein levels 4248 individuals 1458 individuals Illumina [NR] (imputed) 3 cholesteryl ester transfer protein measurement http://www.ebi.ac.uk/efo/EFO_0009133 GCST005672 Genome-wide genotyping array 2019-10-29 30305743 Bycroft C 2018-10-10 Nature www.ncbi.nlm.nih.gov/pubmed/30305743 The UK Biobank resource with deep phenotyping and genomic data. Height 343,321 British ancestry individuals 253,288 European ancestry individuals Affymetrix [16443622] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST008974 Genome-wide genotyping array 2019-08-05 31043758 Warrington NM 2019-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31043758 Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Offspring birth weight 210,267 European ancestry individuals, 19,802 individuals NR Affymetrix, Illumina [14869762] (imputed) 133 birth weight, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0005939 GCST008363 Genome-wide genotyping array 2019-08-05 31043758 Warrington NM 2019-05-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31043758 Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors. Birth weight 298,142 European ancestry individuals, 6,635 African American individuals, 1,449 Filipino individuals, 420 Turkish individuals, 365 Moroccan individuals, 395 Surinamese individuals, 1,052 Afro-Caribbean individuals, 612 Hispanic individuals, 1,180 Thai individuals, 840 Chinese ancestry individuals, 10,133 individuals NR Affymetrix, Illumina [15144367] (imputed) 225 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST008362 Genome-wide genotyping array 2019-02-06 29520040 Coleman JRI 2018-03-08 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29520040 Biological annotation of genetic loci associated with intelligence in a meta-analysis of 87,740 individuals. Extremely high intelligence 1,247 European ancestry cases, 86,493 European ancestry controls NA Illumina [up to 12595966] (imputed) 25 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST007044 Genome-wide genotyping array 2018-12-19 30304924 Kim HJ 2018-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/30304924 Identification of LEF1 as a Susceptibility Locus for Kawasaki Disease in Patients Younger than 6 Months of Age. Kawasaki disease 296 Korean ancestry cases, 1,000 Korean ancestry controls 2,666 East Asian ancestry cases, 10,446 East Asian ancestry controls Illumina [NR] 0 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST006809 Genome-wide genotyping array 2019-05-07 30651383 Chauhan G 2019-01-16 Neurology www.ncbi.nlm.nih.gov/pubmed/30651383 Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. Small subcortical brain infarct 1,715 European ancestry cases, 187 African American cases, 56 Hispanic ancestry cases, 23 Chinese ancestry cases, 40 Malay ancestry cases, 13,749 European ancestry controls, 807 African American controls, 643 Hispanic ancestry controls, 173 Chinese ancestry controls, 168 Malay ancestry controls 630 European ancestry cases, 5,118 European ancestry controls Affymetrix, Illumina [6824387] (imputed) 0 MRI defined brain infarct http://www.ebi.ac.uk/efo/EFO_0004715 GCST007729 Genome-wide genotyping array 2019-05-07 30651383 Chauhan G 2019-01-16 Neurology www.ncbi.nlm.nih.gov/pubmed/30651383 Genetic and lifestyle risk factors for MRI-defined brain infarcts in a population-based setting. Brain infarct 3,149 European ancestry cases, 402 African American cases, 94 Hispanic ancestry cases, 34 Chinese ancestry cases, 47 Malay ancestry cases, 14,807 European ancestry controls, 1,432 African American controls, 643 Hispanic ancestry controls, 173 Chinese ancestry controls, 168 Malay ancestry controls 1,223 European ancestry cases, 260 Japanese ancestry cases, 5,118 European ancestry controls, 261 Japanese ancestry controls Affymetrix, Illumina [7423334] (imputed) 0 MRI defined brain infarct http://www.ebi.ac.uk/efo/EFO_0004715 GCST007730 Genome-wide genotyping array 2019-07-08 30199657 Xu J 2018-09-10 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/30199657 Omega-3 Fatty Acids and Genome-wide Interaction Analyses Reveal DPP10-Pulmonary Function Association. Pulmonary function (FEV1) x omega-3 PUFA (docosapentaenoic acid) interaction (2df) 11,165 European ancestry individuals, 797 African ancestry individuals 1,141 European ancestry individuals, 546 African ancestry individuals Affymetrix, Illumina [7200000] (imputed) 0 forced expiratory volume, docosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0006809 GCST008101 Genome-wide genotyping array 2019-07-08 30199657 Xu J 2018-09-10 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/30199657 Omega-3 Fatty Acids and Genome-wide Interaction Analyses Reveal DPP10-Pulmonary Function Association. Pulmonary function (FVC) x omega-3 PUFA (docosapentaenoic acid) interaction (2df) 11,165 European ancestry individuals, 797 African ancestry individuals 1,141 European ancestry individuals, 546 African ancestry individuals Affymetrix, Illumina [7200000] (imputed) 0 docosapentaenoic acid measurement, vital capacity http://www.ebi.ac.uk/efo/EFO_0006809, http://www.ebi.ac.uk/efo/EFO_0004312 GCST008100 Genome-wide genotyping array 2019-07-08 30199657 Xu J 2018-09-10 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/30199657 Omega-3 Fatty Acids and Genome-wide Interaction Analyses Reveal DPP10-Pulmonary Function Association. Pulmonary function (FVC) x omega-3 PUFA (docosahexaenoic acid) interaction (2df) 11,165 European ancestry individuals, 797 African ancestry individuals 1,141 European ancestry individuals, 546 African ancestry individuals Affymetrix, Illumina [7200000] (imputed) 1 docosahexaenoic acid measurement, vital capacity http://www.ebi.ac.uk/efo/EFO_0007761, http://www.ebi.ac.uk/efo/EFO_0004312 GCST008099 Genome-wide genotyping array 2019-07-08 30199657 Xu J 2018-09-10 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/30199657 Omega-3 Fatty Acids and Genome-wide Interaction Analyses Reveal DPP10-Pulmonary Function Association. Pulmonary function (FEV1) x omega-3 PUFA (docosahexaenoic acid) interaction (2df) 11,165 European ancestry individuals, 797 African ancestry individuals 1,141 European ancestry individuals, 546 African ancestry individuals Affymetrix, Illumina [7200000] (imputed) 0 docosahexaenoic acid measurement, forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0007761, http://www.ebi.ac.uk/efo/EFO_0004314 GCST008102 Genome-wide genotyping array 2018-10-25 30049742 Terzikhan N 2018-07-26 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/30049742 Heritability and genome-wide association study of diffusing capacity of the lung. Diffusing capacity of the lung for carbon monoxide traits 8,372 European ancestry individuals NA Affymetrix, Illumina [NR] 8 diffusing capacity of the lung for carbon monoxide http://www.ebi.ac.uk/efo/EFO_0009369 GCST006473 Genome-wide genotyping array 2019-02-21 30299488 Wang TM 2018-10-08 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/30299488 Genome-Wide Association Study of Susceptibility Loci for Radiation-Induced Brain Injury. Radiation-induced brain injury in nasopharyngeal carcinoma 243 cases, 839 controls 438 cases, 1,422 controls Illumina [445078] 2 response to radiation, radiation-induced brain injury http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0009704 GCST007200 Genome-wide genotyping array 2019-03-27 30729179 Zenin A 2019-01-30 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30729179 Identification of 12 genetic loci associated with human healthspan. Healthspan 300,447 British ancestry individuals 81,099 European ancestry individuals, 3,073 African ancestry individuals, 6,921 South Asian ancestry individuals, 1,422 Chinese ancestry individuals, 3,799 Caribbean individuals Affymetrix [11309218] (imputed) 2 healthspan http://www.ebi.ac.uk/efo/EFO_0009762 GCST007406 Genome-wide genotyping array 2019-02-01 30315195 Lee KY 2018-10-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30315195 Discovering Genetic Factors for psoriasis through exhaustively searching for significant second order SNP-SNP interactions. Psoriasis 2,280 cases, 2,002 controls NA NR [up to 790527] 136 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST007023 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-cytomegalovirus IgG seropositivity 347 Metropolitan French ancestry cases, 653 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 cytomegalovirus seropositivity http://www.ebi.ac.uk/efo/EFO_0007037 GCST006331 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Epstein-Barr virus nuclear antigen (EBNA) IgG seropositivity 914 Metropolitan French ancestry cases, 86 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Epstein Barr virus nuclear antigen-1 seropositivity http://www.ebi.ac.uk/efo/EFO_0009271 GCST006332 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Epstein-Barr virus viral capsid antigen (VCA) IgG seropositivity 956 Metropolitan French ancestry cases, 44 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Epstein Barr viral capsid antigen seropositivity http://www.ebi.ac.uk/efo/EFO_0009272 GCST006333 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Epstein-Barr virus early antigen (EA) IgG seropositivity 91 Metropolitan French ancestry cases, 909 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Epstein-Barr virus early antigen seropositivity http://www.ebi.ac.uk/efo/EFO_0009338 GCST006330 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-herpes simplex virus 1 IgG seropositivity 645 Metropolitan French ancestry cases, 355 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 HSV1 seropositivity http://www.ebi.ac.uk/efo/EFO_0007050 GCST006334 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-herpes simplex virus 2 IgG seropositivity 208 Metropolitan French ancestry cases, 792 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Herpes simplex virus 2 seropositivity http://www.ebi.ac.uk/efo/EFO_0009339 GCST006335 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-varicella zoster virus IgG seropositivity 931 Metropolitan French ancestry cases, 69 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Varicella zoster virus seropositivity http://www.ebi.ac.uk/efo/EFO_0009340 GCST006336 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-helicobacter pylori IgG seropositivity 175 Metropolitan French ancestry cases, 825 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Helicobacter pylori seropositivity http://www.ebi.ac.uk/efo/EFO_0009341 GCST006337 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Toxoplasma gondii IgG seropositivity 559 Metropolitan French ancestry cases, 441 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Toxoplasma gondii seropositivity http://www.ebi.ac.uk/efo/EFO_0007047 GCST006338 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-influenza A virus IgG seropositivity 777 Metropolitan French ancestry cases, 223 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Influenza A seropositivity http://www.ebi.ac.uk/efo/EFO_0007038 GCST006339 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-measles virus IgG seropositivity 885 Metropolitan French ancestry cases, 115 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Measles virus seropositivity http://www.ebi.ac.uk/efo/EFO_0009342 GCST006340 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-mumps virus IgG seropositivity 912 Metropolitan French ancestry cases, 88 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Mumps virus seropositivity http://www.ebi.ac.uk/efo/EFO_0009343 GCST006341 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-rubella virus IgG seropositivity 935 Metropolitan French ancestry cases, 65 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Rubella virus seropositivity http://www.ebi.ac.uk/efo/EFO_0009344 GCST006342 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-hepatitis B virus surface antigen (HBs) IgG seropositivity 508 Metropolitan French ancestry cases, 492 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Hepatitis B virus surface antigen seropositivity http://www.ebi.ac.uk/efo/EFO_0009345 GCST006356 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-hepatitis B virus core antigen (HBc) IgG seropositivity 15 Metropolitan French ancestry cases, 985 Metropolitan French ancestry controls NA Illumina [5699237] (imputed) 0 Hepatitis B virus core antigen seropositivity http://www.ebi.ac.uk/efo/EFO_0009346 GCST006343 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. IgG levels 1000 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0004565 GCST006357 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. IgM levels 1000 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 serum IgM measurement http://www.ebi.ac.uk/efo/EFO_0004993 GCST006359 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. IgA levels 1000 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 1 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST006360 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. IgE levels 1000 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST006358 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-cytomegalovirus IgG levels 347 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-cytomegalovirus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009347 GCST006344 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Epstein-Barr virus nuclear antigen (EBNA) IgG levels 914 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 2 Epstein Barr virus nuclear antigen 1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0007790 GCST006361 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Epstein-Barr virus viral capsid antigen (VCA) IgG levels 956 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Epstein Barr viral capsid antigen IgG measurement http://www.ebi.ac.uk/efo/EFO_0009274 GCST006362 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Epstein-Barr virus early antigen (EA) IgG levels 91 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-Epstein-Barr virus early antigen IgG measurement http://www.ebi.ac.uk/efo/EFO_0009348 GCST006345 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-herpes simplex virus 1 IgG levels 645 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-herpes simplex virus 1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0009349 GCST006346 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-herpes simplex virus 2 IgG levels 208 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-herpes simplex virus 2 IgG measurement http://www.ebi.ac.uk/efo/EFO_0009350 GCST006347 Genome-wide genotyping array 2019-07-02 30201328 Gusareva ES 2018-08-09 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/30201328 Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease. Alzheimer's disease (SNP x SNP interaction) 788 male cases, 1,455 female cases, 2,362 male controls, 3,655 female controls 3,836 male cases, 6,244 female cases, 8,618 male controls, 11,624 female controls Illumina [312064] 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST008056 Genome-wide genotyping array 2021-06-15 32914890 Li W 2020-09-11 Prostate www.ncbi.nlm.nih.gov/pubmed/32914890 Genome-wide association study identifies novel single nucleotide polymorphisms having age-specific effect on prostate-specific antigen levels. Prostate-specific antigen levels x age interaction 2,394 men 2,137 men Illumina [4428605] (imputed) 0 prostate specific antigen measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0004624, http://www.ebi.ac.uk/efo/EFO_0008007 GCST011906 Genome-wide genotyping array 2018-11-05 30217807 Robinson-Cohen C 2018-09-14 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/30217807 Genetic Variants Associated with Circulating Fibroblast Growth Factor 23. Circulating fibroblast growth factor 23 levels 16,624 European ancestry individuals 4,443 African ancestry individuals Affymetrix, Illumina [NR] (imputed) 19 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST006491 Genome-wide genotyping array 2019-03-27 29936532 Colodro-Conde L 2018-06-23 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/29936532 Association Between Population Density and Genetic Risk for Schizophrenia. Socioeconomic status of place of residence 456,426 European ancestry individuals NA Affymetrix [12272635] (imputed) 0 place of residence measurement http://www.ebi.ac.uk/efo/EFO_0009583 GCST007422 Genome-wide genotyping array 2019-03-27 29936532 Colodro-Conde L 2018-06-23 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/29936532 Association Between Population Density and Genetic Risk for Schizophrenia. Population density of place of residence 504,130 European ancestry individuals NA Affymetrix, Illumina, Perlegen [up to 12272635] (imputed) 0 place of residence measurement http://www.ebi.ac.uk/efo/EFO_0009583 GCST007421 Genome-wide genotyping array 2018-10-17 30145303 Kimbrel NA 2018-07-17 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/30145303 A genome-wide association study of suicide attempts and suicidal ideation in U.S. military veterans. Suicidal ideation 79 European ancestry cases, 59 cases, 654 European ancestry controls, 779 controls NA Illumina [2711511] (imputed) 25 suicidal ideation http://www.ebi.ac.uk/efo/EFO_0004320 GCST006429 Genome-wide genotyping array 2018-10-17 30145303 Kimbrel NA 2018-07-17 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/30145303 A genome-wide association study of suicide attempts and suicidal ideation in U.S. military veterans. Suicide attempts 52 European ancestry cases, 70 cases, 680 European ancestry controls, 767 controls NA Illumina [2711511] (imputed) 22 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST006428 Genome-wide genotyping array 2019-03-18 30643256 Baselmans BML 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643256 Multivariate genome-wide analyses of the well-being spectrum. Life satisfaction 80,852 European ancestry individuals NA NR [NR] 148 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST007337 Genome-wide genotyping array 2019-03-18 30643256 Baselmans BML 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643256 Multivariate genome-wide analyses of the well-being spectrum. Positive affect 410,603 European ancestry individuals NA NR [NR] 191 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST007338 Genome-wide genotyping array 2019-03-18 30643256 Baselmans BML 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643256 Multivariate genome-wide analyses of the well-being spectrum. Neuroticism 523,783 European ancestry individuals 59,206 European ancestry individuals NR [NR] 263 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST007339 Genome-wide genotyping array 2019-03-18 30643256 Baselmans BML 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643256 Multivariate genome-wide analyses of the well-being spectrum. Depressive symptoms 1,067,913 European ancestry individuals 228,033 European ancestry individuals NR [NR] 239 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST007340 Genome-wide genotyping array 2019-03-18 30643256 Baselmans BML 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643256 Multivariate genome-wide analyses of the well-being spectrum. Well-being spectrum (multivariate analysis) 2,083,151 European ancestry individuals 287,239 European ancestry individuals NR [NR] 231 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST007341 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (horizontal position gain) 166 Japanese ancestry individuals NA Affymetrix [554152] 1 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006458 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement in schizophrenia (scanpath length) 60 Japanese ancestry cases NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006459 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (horizontal position gain) 60 Japanese ancestry schizophrenia cases, 166 Japanese ancestry controls NA Affymetrix [554152] 1 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006457 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (scanpath length) 166 Japanese ancestry individuals NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006456 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (scanpath length) 60 Japanese ancestry schizophrenia cases, 166 Japanese ancestry controls NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006455 Genome-wide genotyping array 2018-10-18 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement in schizophrenia (duration of fixations) 60 Japanese ancestry cases NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006454 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (duration of fixations) 166 Japanese ancestry individuals NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006453 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (duration of fixations) 60 Japanese ancestry schizophrenia cases, 166 Japanese ancestry controls NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006452 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement in schizophrenia (integrated eye movement score) 60 Japanese ancestry cases NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006451 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (integrated eye movement score) 166 Japanese ancestry individuals NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006450 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement (integrated eye movement score) 60 Japanese ancestry schizophrenia cases, 166 Japanese ancestry controls NA Affymetrix [554152] 0 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006449 Genome-wide genotyping array 2018-10-19 30120336 Kikuchi M 2018-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30120336 Genome-wide Association Analysis of Eye Movement Dysfunction in Schizophrenia. Eye movement in schizophrenia (horizontal position gain) 60 Japanese ancestry cases NA Affymetrix [554152] 3 eye movement measurement http://www.ebi.ac.uk/efo/EFO_0007699 GCST006448 Genome-wide genotyping array 2019-04-05 29632382 Mahajan A 2018-04-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29632382 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Type 2 diabetes 48,286 European ancestry cases, 250,671 European ancestry controls, 33,126 African American, East Asian, Hispanic/Latino or South Asian cases, 120,161 African American, East Asian, Hispanic/Latino or South Asian controls NA Affymetrix, Illumina [247470] 37 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007515 Targeted genotyping array [Exome array] 2019-04-05 29632382 Mahajan A 2018-04-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29632382 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Type 2 diabetes up to 48,286 European ancestry cases, up to 250,671 European ancestry controls NA Affymetrix, Illumina [247470] 32 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007517 Targeted genotyping array [Exome array] 2019-04-05 29632382 Mahajan A 2018-04-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29632382 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Type 2 diabetes (adjusted for BMI) 48,286 European ancestry cases, 250,671 European ancestry controls, 33,126 African American, East Asian, Hispanic/Latino or South Asian cases, 120,161 African American, East Asian, Hispanic/Latino or South Asian controls NA Affymetrix, Illumina [247470] 35 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007516 Targeted genotyping array [Exome array] 2019-04-05 29632382 Mahajan A 2018-04-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29632382 Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes. Type 2 diabetes (adjusted for BMI) up to 48,286 European ancestry cases, up to 250,671 European ancestry controls NA Affymetrix, Illumina [247470] 35 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007518 Targeted genotyping array [Exome array] 2018-07-19 29662059 Howard DM 2018-04-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29662059 Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. Major depressive disorder (probable) 30,603 British ancestry cases, 143,916 British ancestry controls NA NR [7666894] (imputed) 9 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005904 Genome-wide genotyping array 2018-07-19 29662059 Howard DM 2018-04-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29662059 Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. Major depressive disorder (ICD-10 coded) 8,276 British ancestry cases, 209,308 British ancestry controls NA NR [7666894] (imputed) 4 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005903 Genome-wide genotyping array 2018-07-19 29662059 Howard DM 2018-04-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29662059 Genome-wide association study of depression phenotypes in UK Biobank identifies variants in excitatory synaptic pathways. Depression (broad) 113,769 British ancestry cases, 208,811 British ancestry controls NA NR [7666894] (imputed) 111 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005902 Genome-wide genotyping array 2018-10-10 30054594 MacGregor S 2018-07-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30054594 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. Intraocular pressure 133,492 European ancestry individuals NA Affymetrix, Illumina [up to 40000000] (imputed) 106 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST006394 Genome-wide genotyping array 2018-10-10 30054594 MacGregor S 2018-07-27 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30054594 Genome-wide association study of intraocular pressure uncovers new pathways to glaucoma. Glaucoma 11,018 European ancestry cases, 126,068 European ancestry controls NA Affymetrix [up to 40000000] (imputed) 48 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST006395 Genome-wide genotyping array 2018-06-27 29659830 Warrington NM 2018-04-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29659830 Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Digit length ratio (right hand) 12,636 European ancestry individuals NA Illumina [8400000] (imputed) 11 digit length ratio http://www.ebi.ac.uk/efo/EFO_0004841 GCST005748 Genome-wide genotyping array 2018-06-27 29659830 Warrington NM 2018-04-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29659830 Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Digit length ratio 12,586 European ancestry individuals NA Illumina [8400000] (imputed) 12 digit length ratio http://www.ebi.ac.uk/efo/EFO_0004841 GCST005750 Genome-wide genotyping array 2018-06-27 29659830 Warrington NM 2018-04-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29659830 Genome-wide association study identifies nine novel loci for 2D:4D finger ratio, a putative retrospective biomarker of testosterone exposure in utero. Digit length ratio (left hand) 14,382 European ancestry individuals, 1,279 non-European ancestry individuals NA Illumina [8400000] (imputed) 24 digit length ratio http://www.ebi.ac.uk/efo/EFO_0004841 GCST005749 Genome-wide genotyping array 2018-07-09 29691431 Tikkanen E 2018-04-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29691431 Biological Insights Into Muscular Strength: Genetic Findings in the UK Biobank. Hand grip strength 334,825 British ancestry individuals NA Affymetrix [15275733] (imputed) 139 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST005830 Genome-wide genotyping array 2018-07-09 29691431 Tikkanen E 2018-04-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29691431 Biological Insights Into Muscular Strength: Genetic Findings in the UK Biobank. Hand grip strength 223,215 British ancestry individuals 111,610 British ancestry individuals Affymetrix [15275733] (imputed) 27 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST005829 Genome-wide genotyping array 2020-10-29 32843070 Winkler TW 2020-08-26 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/32843070 Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced disease. Early age-related macular degeneration 14,034 European ancestry cases, 91,214 European ancestry controls NA Affymetrix, Illumina [11702853] (imputed) 8 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST010723 Genome-wide genotyping array 2021-03-22 32961594 Neuvonen M 2020-09-22 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32961594 Identification of Glycochenodeoxycholate 3-O-Glucuronide and Glycodeoxycholate 3-O-Glucuronide as Highly Sensitive and Specific OATP1B1 Biomarkers. Fasting plasma glycodeoxycholate 3-O-glucuronide concentration 356 Finnish ancestry individuals NA Illumina [NR] 1 glycodeoxycholate 3-O-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0011010 GCST011372 Genome-wide genotyping array 2021-03-22 32961594 Neuvonen M 2020-09-22 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/32961594 Identification of Glycochenodeoxycholate 3-O-Glucuronide and Glycodeoxycholate 3-O-Glucuronide as Highly Sensitive and Specific OATP1B1 Biomarkers. Fasting plasma glycochenodeoxycholate 3-O-glucuronide concentration 356 Finnish ancestry individuals NA Illumina [NR] 1 glycochenodeoxycholate 3-O-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0011009 GCST011373 Genome-wide genotyping array 2019-02-06 30251476 Lopez-Mejias R 2018-09-24 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/30251476 A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis. Carotid intima media thickness in rheumatoid arthritis 1,355 Spanish ancestry individuals NA Illumina [63089444] (imputed) 3 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST007040 Genome-wide genotyping array 2019-02-06 30251476 Lopez-Mejias R 2018-09-24 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/30251476 A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis. Cardiovascular event in rheumatoid arthritis 467 Spanish ancestry patients, 2,522 Spanish ancestry controls NA Illumina [63089444] (imputed) 1 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST007041 Genome-wide genotyping array 2019-02-08 30251476 Lopez-Mejias R 2018-09-24 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/30251476 A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis. Ischemic heart disease in rheumatoid arthritis 224 Spanish ancestry patients, 2,765 Spanish ancestry controls NA Illumina [63089444] (imputed) 3 ischemic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0001425 GCST007088 Genome-wide genotyping array 2019-03-27 30251476 Lopez-Mejias R 2018-09-24 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/30251476 A genome-wide association study identifies a 3'UTR genetic variant of RARB associated with carotid intima-media thickness in rheumatoid arthritis. Carotid plaques in rheumatoid arthritis 1,355 Spanish ancestry individuals NA Illumina [63089444] (imputed) 4 carotid atherosclerosis http://www.ebi.ac.uk/efo/EFO_0009783 GCST007425 Genome-wide genotyping array 2019-02-28 30254083 Cousminer DL 2018-09-25 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/30254083 First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes. Latent autoimmune diabetes 2,634 European ancestry cases, 5,947 European ancestry controls 345 European ancestry cases, 1,664 European ancestry controls Affymetrix, Illumina [7868002] (imputed) 3 latent autoimmune diabetes in adults http://www.ebi.ac.uk/efo/EFO_0009706 GCST007245 Genome-wide genotyping array 2019-02-28 30254083 Cousminer DL 2018-09-25 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/30254083 First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes. Latent autoimmune diabetes vs. type 2 diabetes 2,779 European ancestry latent autoimmune diabetes cases, 10,396 European ancestry type 2 diabetes cases NA Affymetrix, Illumina [8328843] (imputed) 4 latent autoimmune diabetes in adults, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0009706, http://purl.obolibrary.org/obo/MONDO_0005148 GCST007246 Genome-wide genotyping array 2019-02-28 30254083 Cousminer DL 2018-09-25 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/30254083 First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes. Latent autoimmune diabetes vs. type 1 diabetes 2,454 European ancestry latent autoimmune diabetes cases, 968 European ancestry type 1 diabetes cases NA Affymetrix, Illumina [8465706] (imputed) 1 type 1 diabetes mellitus, latent autoimmune diabetes in adults http://purl.obolibrary.org/obo/MONDO_0005147, http://www.ebi.ac.uk/efo/EFO_0009706 GCST007247 Genome-wide genotyping array 2019-04-29 30255771 Sarnowski C 2018-09-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/30255771 Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels. Triglyceride levels (parental genotype effect) 173 European ancestry families NA Affymetrix [715787] 7 triglyceride measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0005939 GCST007658 Genome-wide genotyping array 2019-04-29 30255771 Sarnowski C 2018-09-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/30255771 Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels. Triglyceride levels in response to fenofibrate treatment (parental genotype effect) 173 European ancestry families NA Affymetrix [715787] 3 triglyceride measurement, response to fenofibrate, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://purl.obolibrary.org/obo/GO_1901557, http://www.ebi.ac.uk/efo/EFO_0005939 GCST007660 Genome-wide genotyping array 2019-04-29 30255771 Sarnowski C 2018-09-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/30255771 Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels. Triglyceride change in response to fenofibrate (parental genotype effect) 173 European ancestry families NA Affymetrix [715787] 0 triglyceride change measurement, response to fenofibrate, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007681, http://purl.obolibrary.org/obo/GO_1901557, http://www.ebi.ac.uk/efo/EFO_0005939 GCST007659 Genome-wide genotyping array 2019-04-29 30255771 Sarnowski C 2018-09-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/30255771 Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels. Triglyceride levels 173 European ancestry families NA Affymetrix [715787] 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST007661 Genome-wide genotyping array 2019-04-29 30255771 Sarnowski C 2018-09-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/30255771 Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels. Triglyceride levels in response to fenofibrate 173 European ancestry families NA Affymetrix [715787] 0 triglyceride measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0004530, http://purl.obolibrary.org/obo/GO_1901557 GCST007662 Genome-wide genotyping array 2019-04-29 30255771 Sarnowski C 2018-09-17 BMC Genet www.ncbi.nlm.nih.gov/pubmed/30255771 Investigation of parent-of-origin effects induced by fenofibrate treatment on triglycerides levels. Triglyceride change in response to fenofibrate treatment 173 European ancestry families NA Affymetrix [715787] 0 triglyceride change measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0007681, http://purl.obolibrary.org/obo/GO_1901557 GCST007663 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Emotional support seeking 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 coping behaviour measurement http://www.ebi.ac.uk/efo/EFO_0009480 GCST006819 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Positive reappraisal 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 coping behaviour measurement http://www.ebi.ac.uk/efo/EFO_0009480 GCST006820 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Problem solving 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 coping behaviour measurement http://www.ebi.ac.uk/efo/EFO_0009480 GCST006821 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Disengagement 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 coping behaviour measurement http://www.ebi.ac.uk/efo/EFO_0009480 GCST006822 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Emotional coping (emotional expression/emotional support seeking) 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 coping behaviour measurement http://www.ebi.ac.uk/efo/EFO_0009480 GCST006823 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Approach coping (positive reappraisal/problem solving) 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 coping behaviour measurement http://www.ebi.ac.uk/efo/EFO_0009480 GCST006824 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Perceived stress 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST006825 Genome-wide genotyping array 2018-12-19 29665250 Shimanoe C 2018-04-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/29665250 A genome-wide association study of coping behaviors suggests FBXO45 is associated with emotional expression. Emotional expression 6,403 Japanese ancestry individuals 7,685 Japanese ancestry individuals Illumina [7094228] (imputed) 0 coping behaviour measurement http://www.ebi.ac.uk/efo/EFO_0009480 GCST006826 Genome-wide genotyping array 2019-02-20 30267110 Kwon YC 2018-09-28 Pediatr Cardiol www.ncbi.nlm.nih.gov/pubmed/30267110 Identification of the TIFAB Gene as a Susceptibility Locus for Coronary Artery Aneurysm in Patients with Kawasaki Disease. Coronary artery aneurysm in Kawasaki disease 33 cases, 215 controls 12 cases, 532 controls Illumina [~ 1000000] 1 coronary aneurysm http://www.ebi.ac.uk/efo/EFO_1000881 GCST007192 Genome-wide genotyping array 2019-05-15 30868120 Berghuis B 2019-01-17 Epilepsia Open www.ncbi.nlm.nih.gov/pubmed/30868120 A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Sodium levels in epilepsy 1,252 European ancestry cases NA Illumina [NR] 1 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST007814 Genome-wide genotyping array 2019-05-15 30868120 Berghuis B 2019-01-17 Epilepsia Open www.ncbi.nlm.nih.gov/pubmed/30868120 A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Carbamazepine- or oxcarbazepine-induced hyponatremia in epilepsy 448 European ancestry cases, 804 European ancestry controls NA Illumina [NR] 3 carbamazepine-induced hyponatremia, response to oxcarbazepine, oxcarbazepine-induced hyponatremia, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0009894, http://www.ebi.ac.uk/efo/EFO_0009893, http://www.ebi.ac.uk/efo/EFO_0009895, http://www.ebi.ac.uk/efo/EFO_0008484 GCST007809 Genome-wide genotyping array 2019-05-15 30868120 Berghuis B 2019-01-17 Epilepsia Open www.ncbi.nlm.nih.gov/pubmed/30868120 A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Severe carbamazepine- or oxcarbazepine-induced hyponatremia in epilepsy 61 European ancestry cases, at least 804 European ancestry controls NA Illumina [NR] 3 carbamazepine-induced hyponatremia, response to oxcarbazepine, oxcarbazepine-induced hyponatremia, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0009894, http://www.ebi.ac.uk/efo/EFO_0009893, http://www.ebi.ac.uk/efo/EFO_0009895, http://www.ebi.ac.uk/efo/EFO_0008484 GCST007810 Genome-wide genotyping array 2019-05-15 30868120 Berghuis B 2019-01-17 Epilepsia Open www.ncbi.nlm.nih.gov/pubmed/30868120 A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Carbamazepine-induced hyponatremia in epilepsy 331 European ancestry cases, 700 European ancestry controls NA Illumina [NR] 7 carbamazepine-induced hyponatremia, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0009894, http://www.ebi.ac.uk/efo/EFO_0008484 GCST007811 Genome-wide genotyping array 2019-05-15 30868120 Berghuis B 2019-01-17 Epilepsia Open www.ncbi.nlm.nih.gov/pubmed/30868120 A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Oxcarbazepine-induced hyponatremia in epilepsy 170 European ancestry cases, 127 European ancestry controls NA Illumina [NR] 1 response to oxcarbazepine, oxcarbazepine-induced hyponatremia http://www.ebi.ac.uk/efo/EFO_0009893, http://www.ebi.ac.uk/efo/EFO_0009895 GCST007812 Genome-wide genotyping array 2019-05-15 30868120 Berghuis B 2019-01-17 Epilepsia Open www.ncbi.nlm.nih.gov/pubmed/30868120 A genome-wide association study of sodium levels and drug metabolism in an epilepsy cohort treated with carbamazepine and oxcarbazepine. Carbamazepine metabolism (carbamazepine-10,11-diol to carbamazepine ratio) in epilepsy 468 European ancestry cases NA Illumina [NR] 3 carbamazepine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0009891 GCST007813 Genome-wide genotyping array 2021-01-06 32963334 Wei XT 2020-09-22 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32963334 Pleiotropic genomic variants at 17q21.31 associated with bone mineral density and body fat mass: a bivariate genome-wide association analysis. Bone mineral density (hip) 10,070 European ancestry individuals, 1,623 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals NA Affymetrix, Illumina [2374420] (imputed) 8 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST010921 Genome-wide genotyping array 2021-01-06 32963334 Wei XT 2020-09-22 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32963334 Pleiotropic genomic variants at 17q21.31 associated with bone mineral density and body fat mass: a bivariate genome-wide association analysis. Body fat mass 10,070 European ancestry individuals, 1,623 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals NA Affymetrix, Illumina [2374420] (imputed) 3 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST010920 Genome-wide genotyping array 2021-01-06 32963334 Wei XT 2020-09-22 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32963334 Pleiotropic genomic variants at 17q21.31 associated with bone mineral density and body fat mass: a bivariate genome-wide association analysis. Hip bone mineral density and total body fat mass (bivariate analysis) 10,070 European ancestry individuals, 1,623 Han Chinese ancestry individuals, 843 African American individuals, 445 Hispanic individuals NA Affymetrix, Illumina [2374420] (imputed) 14 hip bone mineral density, fat body mass http://www.ebi.ac.uk/efo/EFO_0007702, http://www.ebi.ac.uk/efo/EFO_0005409 GCST010922 Genome-wide genotyping array 2020-12-10 32999390 Trajanoska K 2020-09-30 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32999390 Genetic basis of falling risk susceptibility in the UK Biobank Study. Falling risk 89,076 European ancestry cases, 362,103 European ancestry controls 2,215 cases, 6289 controls Affymetrix [7745390] (imputed) 16 Postural instability http://purl.obolibrary.org/obo/HP_0002172 GCST90012857 Genome-wide genotyping array 2019-06-21 30674050 Spiegel AM 2019-01-23 Am J Perinatol www.ncbi.nlm.nih.gov/pubmed/30674050 A Genome-Wide Analysis of Clinical Chorioamnionitis among Preterm Infants. Maternal chorioamnionitis 213 preterm birth infant cases, 707 preterm birth infant controls Illumina [2384515] 0 chorioamnionitis http://www.ebi.ac.uk/efo/EFO_0009948 GCST007956 Genome-wide genotyping array 2019-04-03 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Skin pigmentation traits 4,988 Spanish ancestry individuals NA Illumina [9499600] (imputed) 43 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST007488 Genome-wide genotyping array 2019-04-03 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Hair morphology traits 4,988 Spanish ancestry individuals NA Illumina [9499600] (imputed) 33 hair morphology measurement http://www.ebi.ac.uk/efo/EFO_0007821 GCST007486 Genome-wide genotyping array 2019-04-03 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Anthropometric traits (multi-trait analysis) 4,988 Spanish ancestry individuals 336,107 British ancestry individuals Illumina [9499600] (imputed) 29 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST007490 Genome-wide genotyping array 2019-04-03 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Anthropometric traits 4,988 Spanish ancestry individuals 336,107 British ancestry individuals Illumina [9499600] (imputed) 15 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST007485 Genome-wide genotyping array 2019-04-02 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Disorders of lipid metabolism 4,988 Spanish ancestry individuals NA Illumina [9499600] (imputed) 1 Abnormal circulating lipid concentration http://purl.obolibrary.org/obo/HP_0003119 GCST007480 Genome-wide genotyping array 2019-04-03 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Eye color traits 4,988 Spanish ancestry individuals NA Illumina [9499600] (imputed) 13 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST007489 Genome-wide genotyping array 2019-04-02 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Handedness 4,988 Spanish ancestry individuals NA Illumina [9499600] (imputed) 1 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST007482 Genome-wide genotyping array 2019-04-02 30166351 Galvan-Femenia I 2018-08-30 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30166351 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. Heart rate 4,988 Spanish ancestry individuals NA Illumina [9499600] (imputed) 1 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST007481 Genome-wide genotyping array 2018-08-03 27479909 Hyde CL 2016-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/27479909 Identification of 15 genetic loci associated with risk of major depression in individuals of European descent. Major depressive disorder 84,847 European ancestry cases, 241,266 European ancestry controls 45,773 European ancestry cases, 106,354 European ancestry controls Illumina [1220000] (imputed) 47 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST006041 Genome-wide genotyping array 2018-07-19 29728651 Li X 2018-04-27 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/29728651 Common variants on 6q16.2, 12q24.31 and 16p13.3 are associated with major depressive disorder. Major depressive disorder 84,847 European ancestry cases, 241,266 European ancestry controls, 5,303 Han Chinese ancestry cases, 5,337 Han Chinese ancestry controls 2,659 European ancestry cases, 17,237 European ancestry controls Affymetrix, Illumina [at least 1235109] (imputed) 13 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005907 Genome-wide genotyping array 2018-07-11 29631748 McCoy TH Jr. 2018-03-10 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/29631748 Genome-wide association identifies a novel locus for delirium risk. Delirium 421 European ancestry cases, 5,614 European ancestry controls NA Illumina [up to 1747639] (imputed) 27 delirium http://www.ebi.ac.uk/efo/EFO_0009267 GCST005851 Genome-wide genotyping array 2018-10-19 30093612 O'Mara TA 2018-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30093612 Identification of nine new susceptibility loci for endometrial cancer. Endometrial cancer (endometrioid histology) 8,758 European ancestry cases, 46,126 European ancestry controls NA Affymetrix, Illumina [~ 11700000] (imputed) 32 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST006465 Genome-wide genotyping array 2018-10-19 30093612 O'Mara TA 2018-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30093612 Identification of nine new susceptibility loci for endometrial cancer. Endometrial cancer (Non-endometrioid histology) 1,230 European ancestry cases, 35,447 European ancestry controls NA Affymetrix, Illumina [~ 11700000] (imputed) 7 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST006466 Genome-wide genotyping array 2018-10-19 30093612 O'Mara TA 2018-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30093612 Identification of nine new susceptibility loci for endometrial cancer. Endometrial cancer 12,906 European ancestry cases, 108,979 European ancestry controls NA Affymetrix, Illumina [~ 11700000] (imputed) 28 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST006464 Genome-wide genotyping array 2018-12-14 30305740 Elliott LT 2018-10-10 Nature www.ncbi.nlm.nih.gov/pubmed/30305740 Genome-wide association studies of brain imaging phenotypes in UK Biobank. Brain imaging measurements 8,428 British ancestry individuals 4,386 European ancestry individuals NR [11734353] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST006777 Genome-wide genotyping array 2018-11-01 30130595 Dominguez-Cruz MG 2018-08-18 Gene www.ncbi.nlm.nih.gov/pubmed/30130595 Pilot genome-wide association study identifying novel risk loci for type 2 diabetes in a Maya population. Type 2 diabetes 45 Maya ancestry cases, 47 Maya ancestry controls NA Affymetrix [757439] 24 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST006484 Genome-wide genotyping array 2018-11-30 30294719 Zeng Y 2018-08-24 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/30294719 Sex Differences in Genetic Associations With Longevity. Longevity 564 Han Chinese ancestry male centenarian cases, 1,614 Han Chinese ancestry female centenarian cases, 773 Han Chinese ancestry male middle-aged controls, 1,526 Han Chinese ancestry female middle-aged controls NA Illumina [5595657] (imputed) 20 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST006658 Genome-wide genotyping array 2019-05-08 30854688 Wang C 2019-03-10 Hepatology www.ncbi.nlm.nih.gov/pubmed/30854688 Genome Wide Association Studies of Specific Antinuclear Autoantibody Sub-phenotypes in Primary Biliary Cholangitis. Anti-sp100 seropositivity in primary biliary cholangitis 211 Han Chinese ancestry cases, 711 Han Chinese ancestry controls 234 Han Chinese ancestry cases, 1,018 Han Chinese ancestry controls Illumina [794531] 2 antinuclear antibody measurement http://www.ebi.ac.uk/efo/EFO_0005949 GCST007737 Genome-wide genotyping array 2019-05-08 30854688 Wang C 2019-03-10 Hepatology www.ncbi.nlm.nih.gov/pubmed/30854688 Genome Wide Association Studies of Specific Antinuclear Autoantibody Sub-phenotypes in Primary Biliary Cholangitis. Anti-gp210 seropositivity in primary biliary cholangitis 350 Han Chinese ancestry cases, 562 Han Chinese ancestry controls 444 Han Chinese ancestry cases, 808 Han Chinese ancestry controls Illumina [794694] 0 antinuclear antibody measurement http://www.ebi.ac.uk/efo/EFO_0005949 GCST007736 Genome-wide genotyping array 2018-05-25 29731509 Zabaneh D 2017-07-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29731509 A genome-wide association study for extremely high intelligence. Extremely high intelligence 1,238 European ancestry cases, 8,172 European ancestry controls NA Illumina [6773587] (imputed) 1 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST005626 Genome-wide genotyping array 2019-01-10 23830517 Saruhan-Direskeneli G 2013-07-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/23830517 Identification of multiple genetic susceptibility loci in Takayasu arteritis. Takayasu arteritis 305 Turkish ancestry cases, 106 European ancestry cases, 483 Turkish ancestry controls, 553 European ancestry controls NA Illumina [at least 124312] 5 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST006863 Targeted genotyping array [ImmunoChip] 2019-02-14 30261039 Suri P 2018-09-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30261039 Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain. Chronic back pain 29,531 European ancestry cases, 128,494 European ancestry controls 50,915 British ancestry cases, 232,837 British ancestry controls Affymetrix, Illumina [up to 9775703] (imputed) 4 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST007152 Genome-wide genotyping array 2019-01-25 26490195 Cleynen I 2015-10-18 Lancet www.ncbi.nlm.nih.gov/pubmed/26490195 Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study. Inflammatory bowel disease 16,902 European ancestry Crohn's disease cases, 12,597 European ancestry ulcerative colitis cases, 339 European ancestry cases 2,453 European ancestry Crohn's disease cases, 3,729 European ancestry ulcerative colitis cases Illumina [156154] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST006960 Targeted genotyping array [ImmunoChip] 2019-01-16 30305239 Macias-Kauffer LR 2018-10-01 Int J Cardiol www.ncbi.nlm.nih.gov/pubmed/30305239 Genetic contributors to serum uric acid levels in Mexicans and their effect on premature coronary artery disease. Serum uric acid levels 2153 Mexican ancestry individuals NA Illumina [865896] (imputed) 3 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST006905 Genome-wide genotyping array 2019-02-13 30298529 Stanaway IB 2018-10-08 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30298529 The eMERGE genotype set of 83,717 subjects imputed to ~40 million variants genome wide and association with the herpes zoster medical record phenotype. Shingles 3,201 European ancestry cases, 34,960 European ancestry controls, 398 African American cases, 5,922 African American controls, 756 Asian ancestry individuals NA Affymetrix, Illumina [39127678] (imputed) 11 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST007139 Genome-wide genotyping array 2018-11-07 24869959 Jacobs LC 2014-08-01 JAMA Dermatol www.ncbi.nlm.nih.gov/pubmed/24869959 Intrinsic and extrinsic risk factors for sagging eyelids. Upper eyelid sagging severity 6,631 European ancestry individuals NA Illumina [at least 2149245] (imputed) 22 eyelid sagging measurement http://www.ebi.ac.uk/efo/EFO_0009360 GCST006522 Genome-wide genotyping array 2019-04-24 28346466 Chen G 2017-03-27 PLoS One www.ncbi.nlm.nih.gov/pubmed/28346466 Common and rare exonic MUC5B variants associated with type 2 diabetes in Han Chinese. Type 2 diabetes 1,908 Han Chinese ancestry individuals 10,401 African ancestry individuals Illumina [up to 178943] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST007620 Targeted genotyping array [Exome array] 2018-11-28 30196971 Bray MJ 2018-09-01 Fertil Steril www.ncbi.nlm.nih.gov/pubmed/30196971 Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women. Uterine fibroid number (single vs multiple) 636 African American or European ancestry female individuals with single fibroid, 822 African American or European ancestry female individuals with multiple fibroids NA Affymetrix [up to 9627525] (imputed) 8 uterine fibroid measurement http://www.ebi.ac.uk/efo/EFO_0009410 GCST006616 Genome-wide genotyping array 2018-11-28 30196971 Bray MJ 2018-09-01 Fertil Steril www.ncbi.nlm.nih.gov/pubmed/30196971 Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women. Uterine fibroid size (maximum dimension) 1,301 African American or European ancestry female individuals NA Affymetrix [up to 9596033] (imputed) 5 uterine fibroid measurement http://www.ebi.ac.uk/efo/EFO_0009410 GCST006618 Genome-wide genotyping array 2018-11-28 30196971 Bray MJ 2018-09-01 Fertil Steril www.ncbi.nlm.nih.gov/pubmed/30196971 Transethnic and race-stratified genome-wide association study of fibroid characteristics in African American and European American women. Uterine fibroid size (maximum volume) 1,048 African American or European ancestry female individuals NA Affymetrix [up to 9597202] (imputed) 6 uterine fibroid measurement http://www.ebi.ac.uk/efo/EFO_0009410 GCST006617 Genome-wide genotyping array 2019-03-19 30207284 Galvan-Femenia I 2018-03-01 Cancer Treat Res Commun www.ncbi.nlm.nih.gov/pubmed/30207284 Genomic profiling in advanced stage non-small-cell lung cancer patients with platinum-based chemotherapy identifies germline variants with prognostic value in SMYD2. Response to platinum-based chemotherapy in non-small-cell lung cancer (progression) 181 European ancestry individuals 356 European ancestry individuals Illumina [10307177] (imputed) 0 response to platinum based chemotherapy, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0008336 GCST007358 Genome-wide genotyping array 2019-02-11 30277654 Yokoshima Y 2018-09-14 Neuropsychopharmacol Rep www.ncbi.nlm.nih.gov/pubmed/30277654 Gamma-aminobutyric acid transaminase genetic polymorphism is a candidate locus for responsiveness to opioid analgesics in patients with cancer pain: An exploratory study. Response to opioid analgesics in cancer (pain decrease) 71 Japanese ancestry individuals NA Illumina [771433] 2 response to opioid http://www.ebi.ac.uk/efo/EFO_0008541 GCST007106 Genome-wide genotyping array 2022-07-12 35739095 Pujol-Gualdo N 2022-06-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35739095 Advancing our understanding of genetic risk factors and potential personalized strategies for pelvic organ prolapse. Pelvic organ prolapse 28,086 European ancestry cases, 546,291 European ancestry controls NA Affymetrix, Illumina [15065244] (imputed) 30 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90102470 Genome-wide genotyping array 2021-05-10 32853455 Schwantes-An TH 2020-08-27 Hepatology www.ncbi.nlm.nih.gov/pubmed/32853455 Genome-wide association study and meta-analysis on alcohol-related liver cirrhosis identifies novel genetic risk factors. Cirrhosis (alcohol related) 1,128 European ancestry cases, 849 European ancestry heavy-drinking controls up to 2,369 European ancestry cases, up to 10,434 European ancestry heavy-drinking controls Illumina [9377111] (imputed) 14 alcoholic liver cirrhosis http://www.ebi.ac.uk/efo/EFO_1000802 GCST011639 Genome-wide genotyping array 2021-04-07 32841424 Herrera-Luis E 2020-08-25 Pediatr Allergy Immunol www.ncbi.nlm.nih.gov/pubmed/32841424 Genome-wide association study reveals a novel locus for asthma with severe exacerbations in diverse populations. Asthma with severe exacerbations 1,283 Latino cases, 2,027 Latino controls 448 African American cases, 595 African American controls Affymetrix [9737707] (imputed) 21 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST011457 Genome-wide genotyping array 2020-09-12 32835660 Shin JG 2020-08-21 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/32835660 Genome-wide association analysis of 17,019 Korean women identifies variants associated with facial pigmented spots. Facial pigmentation measurement (UV light) 11,079 Korean women 5,940 Korean women Illumina [366864] (imputed) 7 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST90002283 Genome-wide genotyping array 2020-09-12 32835660 Shin JG 2020-08-21 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/32835660 Genome-wide association analysis of 17,019 Korean women identifies variants associated with facial pigmented spots. Facial pigmentation measurement (polar light) 11,079 Korean women 5,940 Korean women Illumina [366864] (imputed) 7 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST90002284 Genome-wide genotyping array 2018-10-19 30220432 Haas ME 2018-09-06 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30220432 Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. Urinary albumin excretion (no hypertensive medication) 302,687 European ancestry individuals without hypertensive medication NA Affymetrix [11709857] (imputed) 23 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST006463 Genome-wide genotyping array 2018-11-19 30220432 Haas ME 2018-09-06 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30220432 Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. Urinary albumin excretion 382,500 European ancestry individuals NA Affymetrix [11709857] (imputed) 46 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST006586 Genome-wide genotyping array 2018-07-19 29631575 Obeidat M 2018-04-10 Respir Res www.ncbi.nlm.nih.gov/pubmed/29631575 The genetics of smoking in individuals with chronic obstructive pulmonary disease. Cotinine levels in smokers with chronic obstructive pulmonary disease 4,024 European ancestry individuals NA Illumina [7807992] (imputed) 2 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST005916 Genome-wide genotyping array 2018-07-19 29631575 Obeidat M 2018-04-10 Respir Res www.ncbi.nlm.nih.gov/pubmed/29631575 The genetics of smoking in individuals with chronic obstructive pulmonary disease. Current cigarettes per day in chronic obstructive pulmonary disease 2,854 European ancestry individuals NA Illumina [7807992] (imputed) 2 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST005917 Genome-wide genotyping array 2018-07-19 29631575 Obeidat M 2018-04-10 Respir Res www.ncbi.nlm.nih.gov/pubmed/29631575 The genetics of smoking in individuals with chronic obstructive pulmonary disease. Smoking cessation in chronic obstructive pulmonary disease 717 European ancestry sustained quitter cases, 2,175 European ancestry continuous smoker cases NA Illumina [7807992] (imputed) 2 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST005918 Genome-wide genotyping array 2018-07-19 29631575 Obeidat M 2018-04-10 Respir Res www.ncbi.nlm.nih.gov/pubmed/29631575 The genetics of smoking in individuals with chronic obstructive pulmonary disease. Exhaled carbon monoxide levels in smokers with chronic obstructive pulmonary disease 2,706 European ancestry individuals NA Illumina [7807992] (imputed) 3 carbon monoxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0006520 GCST005919 Genome-wide genotyping array 2021-04-06 32839289 Milne S 2020-08-24 Thorax www.ncbi.nlm.nih.gov/pubmed/32839289 Protective effect of club cell secretory protein (CC-16) on COPD risk and progression: a Mendelian randomisation study. Serum CC16 levels 5,552 individuals NA Illumina [7312348] (imputed) 6 CC16 measurement http://www.ebi.ac.uk/efo/EFO_0005080 GCST011456 Genome-wide genotyping array 2018-12-05 30263053 Deng X 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30263053 Genome-wide association study for multiple phenotype analysis. Triglyceride levels 821 individuals NA Affymetrix [587358] 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST006664 Genome-wide genotyping array 2018-12-05 30263053 Deng X 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30263053 Genome-wide association study for multiple phenotype analysis. HDL cholesterol 821 individuals NA Affymetrix [587358] 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST006663 Genome-wide genotyping array 2018-12-06 30263053 Deng X 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30263053 Genome-wide association study for multiple phenotype analysis. HDL cholesterol and triglyceride levels (pleiotropy) 821 individuals NA Affymetrix [587358] 8 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST006669 Genome-wide genotyping array 2019-03-14 30263045 Blackburn NB 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30263045 Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships. High density lipoprotein cholesterol levels 817 individuals NA NR [718407] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007301 Genome-wide genotyping array 2019-03-14 30263045 Blackburn NB 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30263045 Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships. Response to fenofibrate (HDL cholesterol levels) 817 individuals NA NR [718407] 1 high density lipoprotein cholesterol measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0004612, http://purl.obolibrary.org/obo/GO_1901557 GCST007300 Genome-wide genotyping array 2019-03-14 30263045 Blackburn NB 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30263045 Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships. Triglyceride levels 817 individuals NA NR [718407] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST007299 Genome-wide genotyping array 2019-03-14 30263045 Blackburn NB 2018-09-17 BMC Proc www.ncbi.nlm.nih.gov/pubmed/30263045 Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships. Response to fenofibrate (triglyceride levels) 774 individuals NA NR [718407] 0 triglyceride measurement, response to fenofibrate http://www.ebi.ac.uk/efo/EFO_0004530, http://purl.obolibrary.org/obo/GO_1901557 GCST007298 Genome-wide genotyping array 2018-12-11 30248107 Wu S 2018-09-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30248107 Genome-wide association studies and CRISPR/Cas9-mediated gene editing identify regulatory variants influencing eyebrow thickness in humans. Eyebrow thickness 2,961 Han Chinese ancestry individuals, 721 Uyghur ancestry individuals, 2,301 Latin American ancestry individuals 4,411 Dutch ancestry individuals Illumina [up to 7224952] (imputed) 4 facial hair thickness measurement http://www.ebi.ac.uk/efo/EFO_0007823 GCST006706 Genome-wide genotyping array 2019-02-14 30265060 MacKillop J 2018-09-27 Exp Clin Psychopharmacol www.ncbi.nlm.nih.gov/pubmed/30265060 Genetic influences on delayed reward discounting: A genome-wide prioritized subset approach. Delayed reward discounting 986 European ancestry individuals NA Illumina [4883968] (imputed) 5 delayed reward discounting measurement http://www.ebi.ac.uk/efo/EFO_0008476 GCST007153 Genome-wide genotyping array 2018-11-01 30061609 Wyss AB 2018-07-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30061609 Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Lung function (FEV1) 60,552 European ancestry individuals, 8,429 African individuals, 9,959 Korean ancestry individuals, 11,775 Hispanic individuals Affymetrix, Illumina [10900000] (imputed) 56 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST006481 Genome-wide genotyping array 2018-11-01 30061609 Wyss AB 2018-07-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30061609 Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Lung function (FEV1/FVC) 60,552 European ancestry individuals, 8,429 African individuals, 9,959 Korean ancestry individuals, 11,775 Hispanic individuals Affymetrix, Illumina [10900000] (imputed) 39 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST006482 Genome-wide genotyping array 2018-11-01 30061609 Wyss AB 2018-07-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30061609 Multiethnic meta-analysis identifies ancestry-specific and cross-ancestry loci for pulmonary function. Lung function (FVC) 60,552 European ancestry individuals, 8,429 African individuals, 9,959 Korean ancestry individuals, 11,775 Hispanic individuals Affymetrix, Illumina [10900000] (imputed) 69 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST006483 Genome-wide genotyping array 2018-10-18 30108155 Hebbar P 2018-08-14 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/30108155 Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population. High density lipoprotein cholesterol levels 1,353 Kuwaiti ancestry individuals 1,176 Kuwaiti ancestry individuals Illumina [632375] 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST006438 Genome-wide genotyping array 2018-10-18 30108155 Hebbar P 2018-08-14 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/30108155 Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population. Low density lipoprotein cholesterol levels 1,353 Kuwaiti ancestry individuals 1,176 Kuwaiti ancestry individuals Illumina [632375] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST006437 Genome-wide genotyping array 2018-10-18 30108155 Hebbar P 2018-08-14 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/30108155 Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population. Total cholesterol levels 1,353 Kuwaiti ancestry individuals 1,176 Kuwaiti ancestry individuals Illumina [632375] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST006439 Genome-wide genotyping array 2018-10-18 30108155 Hebbar P 2018-08-14 J Lipid Res www.ncbi.nlm.nih.gov/pubmed/30108155 Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population. Triglyceride levels 1,353 Kuwaiti ancestry individuals 1,176 Kuwaiti ancestry individuals Illumina [632375] 15 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST006436 Genome-wide genotyping array 2018-10-15 30104567 Ji X 2018-08-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30104567 Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Lung cancer in ever smokers 4,628 European ancestry cases, 4,041 European ancestry controls 16,341 European ancestry cases, 9,930 European ancestry controls Illumina [20734083] (imputed) 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST006400 Genome-wide genotyping array 2018-10-15 30104567 Ji X 2018-08-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30104567 Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Lung cancer (SNP x SNP interaction) 4,918 European ancestry cases, 5,555 European ancestry controls NA Illumina [2482200] (imputed) 25 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST006398 Genome-wide genotyping array 2018-10-15 30104567 Ji X 2018-08-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30104567 Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Lung cancer 4,918 European ancestry cases, 5,555 European ancestry controls 18,439 European ancestry cases, 14,026 European ancestry controls Illumina [20734083] (imputed) 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST006399 Genome-wide genotyping array 2019-05-07 28817678 Archer NP 2017-08-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/28817678 Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility. Acute lymphoblastic leukemia (childhood) 203 Hispanic cases and 96 Native American cases from 323 families NA Illumina [up to 237436] 2 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST007727 Targeted genotyping array [Exome array] 2018-09-17 30034349 Lin E 2018-07-06 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/30034349 A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers. Response to selective serotonin reuptake inhibitors in depression 257 Taiwanese ancestry responders, 164 Taiwanese ancestry non-responders NA Illumina [4241701] (imputed) 3 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST006267 Genome-wide genotyping array 2018-09-17 30034349 Lin E 2018-07-06 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/30034349 A Deep Learning Approach for Predicting Antidepressant Response in Major Depression Using Clinical and Genetic Biomarkers. Remission after SSRI treatment in major depression 139 Taiwanese ancestry remitted cases, 282 Taiwanese ancestry non-remitted cases NA Illumina [4241701] (imputed) 1 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST006266 Genome-wide genotyping array 2018-10-18 30213928 Went M 2018-09-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30213928 Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma. Multiple myeloma 8,197 European ancestry cases, 241,468 European ancestry controls 1,777 European ancestry cases, 6,088 European ancestry controls Illumina [up to 10291845] (imputed) 9 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST006432 Genome-wide genotyping array 2019-02-11 30217971 Ho KWD 2018-09-14 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30217971 Genome-wide association study of seasonal affective disorder. Seasonality in depression 1,380 European ancestry cases, 2,464 European ancestry controls NA Affymetrix, Illumina [8153767] (imputed) 0 seasonality measurement http://www.ebi.ac.uk/efo/EFO_0006876 GCST007101 Genome-wide genotyping array 2019-02-11 30217971 Ho KWD 2018-09-14 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30217971 Genome-wide association study of seasonal affective disorder. Seasonality and depression 1,380 European ancestry cases, 2,937 European ancestry controls NA Affymetrix, Illumina [8153767] (imputed) 18 unipolar depression, bipolar disorder, seasonality measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0006876 GCST007102 Genome-wide genotyping array 2019-05-07 30850646 Tziotzios C 2019-03-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30850646 Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02. Frontal fibrosing alopecia 1,016 European ancestry cases, 4,145 European ancestry controls Illumina [~ 8000000] (imputed) 37 frontal fibrosing alopecia http://www.ebi.ac.uk/efo/EFO_0009855 GCST007713 Genome-wide genotyping array 2021-03-01 33590662 Heilbronner U 2021-02-15 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/33590662 "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. Emotional lability 3,268 European ancestry individuals NA Illumina [8348463] (imputed) 4 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST90013452 Genome-wide genotyping array 2021-03-01 33590662 Heilbronner U 2021-02-15 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/33590662 "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. Lack of behavioral control 3,268 European ancestry individuals NA Illumina [8348463] (imputed) 7 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90013453 Genome-wide genotyping array 2021-03-01 33590662 Heilbronner U 2021-02-15 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/33590662 "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. Type A behavior 3,268 European ancestry individuals NA Illumina [8348463] (imputed) 4 extraversion measurement http://www.ebi.ac.uk/efo/EFO_0007913 GCST90013454 Genome-wide genotyping array 2021-03-01 33590662 Heilbronner U 2021-02-15 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/33590662 "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. Locus of control over disease 3,268 European ancestry individuals NA Illumina [8348463] (imputed) 2 behavioural inhibitory control measurement http://www.ebi.ac.uk/efo/EFO_0008467 GCST90013455 Genome-wide genotyping array 2021-03-01 33590662 Heilbronner U 2021-02-15 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/33590662 "The Heidelberg Five" personality dimensions: Genome-wide associations, polygenic risk for neuroticism, and psychopathology 20 years after assessment. Psychoticism 3,268 European ancestry individuals NA Illumina [8348463] (imputed) 5 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90013456 Genome-wide genotyping array 2019-03-04 30595539 Wallace HJ 2018-12-27 Burns www.ncbi.nlm.nih.gov/pubmed/30595539 Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study. Postburn scar height 665 European ancestry individuals NA Illumina [298150] 2 postburn hypertrophic scarring severity measurement http://www.ebi.ac.uk/efo/EFO_0007747 GCST007251 Genome-wide genotyping array 2019-03-04 30595539 Wallace HJ 2018-12-27 Burns www.ncbi.nlm.nih.gov/pubmed/30595539 Genetic influence on scar height and pliability after burn injury in individuals of European ancestry: A prospective cohort study. Postburn scar pliability 665 European ancestry individuals NA Illumina [298150] 4 postburn hypertrophic scarring severity measurement http://www.ebi.ac.uk/efo/EFO_0007747 GCST007252 Genome-wide genotyping array 2021-06-03 32912934 Li M 2020-09-10 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/32912934 Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA Nephropathy. IgA nephropathy 2,628 Chinese ancestry cases, 11,563 Chinese ancestry controls 6,879 Han Chinese ancestry cases, 9,019 Han Chinese ancestry controls, 1,039 Italian ancestry cases, 1,289 Italian ancestry controls NR [3611808] (imputed) 12 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST011781 Genome-wide genotyping array 2021-05-26 32830257 Castellucci LC 2020-08-23 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/32830257 A Genome-Wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1 and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis In Brazil. Cutaneous leishmaniasis 2,066 Hispanic/Latino cases, 2,046 Hispanic/Latino controls NR Illumina [4498586] (imputed) 14 cutaneous Leishmaniasis http://www.ebi.ac.uk/efo/EFO_0005046 GCST011739 Genome-wide genotyping array 2019-03-13 30693016 Lin WY 2019-01-14 Front Genet www.ncbi.nlm.nih.gov/pubmed/30693016 Genome-Wide Gene-Environment Interaction Analysis Using Set-Based Association Tests. Diastolic blood pressure x alcohol consumption interaction (1df test) 1,764 Han Chinese and unknown ancestry alcohol drinkers, 14,779 Han Chinese and unknown ancestry non-drinkers NA NR [603741] 1 diastolic blood pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0004329 GCST007287 Genome-wide genotyping array 2019-03-13 30693016 Lin WY 2019-01-14 Front Genet www.ncbi.nlm.nih.gov/pubmed/30693016 Genome-Wide Gene-Environment Interaction Analysis Using Set-Based Association Tests. Systolic blood pressure x alcohol consumption interaction (1df test) 1,764 Han Chinese and unknown ancestry alcohol drinkers, 14,779 Han Chinese and unknown ancestry non-drinkers NA NR [603741] 0 systolic blood pressure, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004329 GCST007288 Genome-wide genotyping array 2019-02-20 30266950 Miyagawa T 2018-09-28 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30266950 A variant at 9q34.11 is associated with HLA-DQB1*06:02 negative essential hypersomnia. Hypersomnia (HLA-DQB1*06:02 negative) 119 Japanese ancestry cases, 1,582 Japanese ancestry controls 283 Japanese ancestry cases, 433 Japanese ancestry controls Affymetrix [476572] 1 hypersomnia http://www.ebi.ac.uk/efo/EFO_0005246 GCST007191 Genome-wide genotyping array 2021-05-24 32897244 Zhang L 2020-09-07 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/32897244 Identification of cardiovascular health gene variants related to longevity in a Chinese population. Longevity 395 Chinese ancestry cases, 301 Chinese ancestry controls 4,712 Chinese ancestry cases, 7,867 Chinese ancestry controls Affymetrix [5600000] 0 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST011719 Genome-wide genotyping array 2018-07-13 29632305 Lee HS 2018-04-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29632305 New Common and Rare Variants Influencing Metabolic Syndrome and Its Individual Components in a Korean Population. Metabolic syndrome (multivariate analysis) 1,946 Korean ancestry cases, 6,427 Korean ancestry controls 430 Korean ancestry cases, 3,264 Korean ancestry controls Affymetrix [344366] 10 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST005878 Genome-wide genotyping array 2018-08-03 29650764 McDonough CW 2018-04-01 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/29650764 Genetic Variants Influencing Plasma Renin Activity in Hypertensive Patients From the PEAR Study (Pharmacogenomic Evaluation of Antihypertensive Responses). Plasma renin activity levels 461 European ancestry individuals, 297 African American ancestry individuals 150 European ancestry individuals Illumina [up to 1000000] (imputed) 3 plasma renin activity measurement http://www.ebi.ac.uk/efo/EFO_0006828 GCST006043 Genome-wide genotyping array 2019-01-28 30305637 McMaster ML 2018-10-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30305637 Two high-risk susceptibility loci at 6p25.3 and 14q32.13 for Waldenström macroglobulinemia. Waldenström macroglobulinemia / lymphoplasmacytic lymphoma 217 European ancestry cases, 3,798 European ancestry controls 313 European ancestry cases, 564 European ancestry controls Illumina [6440053] (imputed) 3 Waldenstrom macroglobulinemia http://www.ebi.ac.uk/efo/EFO_0009441 GCST006982 Genome-wide genotyping array 2018-09-11 29730043 Li J 2018-05-02 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/29730043 Identifying the genetic risk factors for treatment response to lurasidone by genome-wide association study: A meta-analysis of samples from three independent clinical trials. Response to lurasidone in schizophrenia 264 European ancestry cases, 158 African American ancestry cases NA Affymetrix, Illumina [up to 1994688] 13 response to antipsychotic drug http://purl.obolibrary.org/obo/GO_0097332 GCST006248 Genome-wide genotyping array 2018-06-21 29725004 Hosoda Y 2018-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29725004 CCDC102B confers risk of low vision and blindness in high myopia. Myopic maculopathy 4,476 Japanese ancestry individuals 3,279 Japanese ancestry individuals Illumina [4710779] (imputed) 1 myopic maculopathy severity measurement http://www.ebi.ac.uk/efo/EFO_0009177 GCST005715 Genome-wide genotyping array, Exome genotyping array 2021-04-19 33585033 Hayashi S 2021-01-29 Biomed Rep www.ncbi.nlm.nih.gov/pubmed/33585033 A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis. joint destruction in rheumatoid arthritis (rapid vs slow) 32 Japanese ancestry rapid joint destruction individuals, 208 Japanese ancestry slow joint destruction individuals NA Illumina [up to 317503] 9 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST011517 Genome-wide genotyping array 2021-04-19 33585033 Hayashi S 2021-01-29 Biomed Rep www.ncbi.nlm.nih.gov/pubmed/33585033 A genome-wide association study identifying the SNPs predictive of rapid joint destruction in patients with rheumatoid arthritis. joint destruction in rheumatoid arthritis (rapid vs slow) 30 Japanese ancestry rapid joint destruction individuals, 198 Japanese ancestry slow joint destruction individuals NA Illumina [up to 317503] 10 joint damage measurement http://www.ebi.ac.uk/efo/EFO_0005413 GCST011516 Genome-wide genotyping array 2019-02-14 30266756 Chang X 2018-09-28 J Med Genet www.ncbi.nlm.nih.gov/pubmed/30266756 Common variants at 5q33.1 predispose to migraine in African-American children. Paediatric migraine 380 African American cases, 2,129 African American controls, 599 European American cases, 7,327 European American controls 233 African American cases, 4,038 African American controls Illumina [up to 522471] 2 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST007154 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-varicella zoster virus IgG levels 931 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-varicella zoster virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009351 GCST006348 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-helicobacter pylori IgG levels 175 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 anti-Helicobacter pylori serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0005247 GCST006363 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-Toxoplasma gondii IgG levels 559 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-Toxoplasma gondii IgG measurement http://www.ebi.ac.uk/efo/EFO_0009353 GCST006349 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-influenza A virus IgG levels 777 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-influenza A virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009354 GCST006350 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-measles virus IgG levels 885 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-measles virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009355 GCST006351 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-mumps virus IgG levels 912 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-mumps virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009356 GCST006352 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-rubella virus IgG levels 935 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 2 Anti-rubella virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009357 GCST006353 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-hepatitis B virus surface antigen (HBs) IgG levels 508 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-hepatitis B virus surface antigen IgG measurement http://www.ebi.ac.uk/efo/EFO_0009358 GCST006354 Genome-wide genotyping array 2018-09-25 30053915 Scepanovic P 2018-07-27 Genome Med www.ncbi.nlm.nih.gov/pubmed/30053915 Human genetic variants and age are the strongest predictors of humoral immune responses to common pathogens and vaccines. Anti-hepatitis B virus core antigen (HBc) IgG levels 15 Metropolitan French ancestry individuals NA Illumina [5699237] (imputed) 0 Anti-hepatitis B virus core antigen IgG measurement http://www.ebi.ac.uk/efo/EFO_0009359 GCST006355 Genome-wide genotyping array 2018-10-12 30120083 Ferguson A 2018-08-14 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/30120083 Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability. Relative amplitude of rest-activity cycles 77,440 European ancestry individuals NA Affymetrix [7969123] (imputed) 13 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST006397 Genome-wide genotyping array 2018-10-12 30120083 Ferguson A 2018-08-14 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/30120083 Genome-Wide Association Study of Circadian Rhythmicity in 71,500 UK Biobank Participants and Polygenic Association with Mood Instability. Disrupted circadian rhythm (low relative amplitude of rest-activity cycles) at least 2,700 European ancestry cases, at least 68,300 European ancestry controls NA Affymetrix [7969123] (imputed) 10 circadian rhythm http://www.ebi.ac.uk/efo/EFO_0004354 GCST006396 Genome-wide genotyping array 2019-01-04 30196823 Blum S 2018-08-02 J Neuroimmunol www.ncbi.nlm.nih.gov/pubmed/30196823 Genome-wide association study in Guillain-Barré syndrome. Guillain-Barré syndrome 191 European ancestry cases, 639 European ancestry controls NA Illumina [579499] 0 Guillain-Barre syndrome http://www.ebi.ac.uk/efo/EFO_0007292 GCST006836 Genome-wide genotyping array 2022-03-07 34776419 Brolin K 2021-11-07 J Parkinsons Dis www.ncbi.nlm.nih.gov/pubmed/34776419 Insights on Genetic and Environmental Factors in Parkinson's Disease from a Regional Swedish Case-Control Cohort. Parkinson's disease 929 Swedish ancestry cases, 935 Swedish ancestry controls NA Illumina [5445841] (imputed) 3 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90095083 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androsterone sulfate levels in chronic kidney disease 395 European ancestry individuals NA Illumina [7747945] (imputed) 0 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90264812 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine anserine levels in chronic kidney disease 2,442 European ancestry individuals NA Illumina [7723595] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264813 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine anthranilate levels in chronic kidney disease 3,618 European ancestry individuals NA Illumina [7722106] (imputed) 1 anthranilate measurement http://www.ebi.ac.uk/efo/EFO_0800123 GCST90264814 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arabinose levels in chronic kidney disease 3,468 European ancestry individuals NA Illumina [7723236] (imputed) 0 arabinose measurement http://www.ebi.ac.uk/efo/EFO_0021030 GCST90264815 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine arabinose levels in chronic kidney disease 4,806 European ancestry individuals NA Illumina [7723038] (imputed) 0 arabinose measurement http://www.ebi.ac.uk/efo/EFO_0021030 GCST90264816 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arabitol/xylitol levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264817 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine arabitol/xylitol levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723580] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264818 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arabonate/xylonate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723663] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264819 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine arabonate/xylonate levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723463] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264820 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arachidate (20:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 arachidate (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800625 GCST90264821 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arachidonate (20:4n6) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90264822 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arachidonoylcarnitine (C20:4) levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724593] (imputed) 3 arachidonoylcarnitine (C20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800544 GCST90264823 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arachidonoylcholine levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723436] (imputed) 1 arachidonoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800478 GCST90264824 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arachidoylcarnitine (C20)* levels in chronic kidney disease 4,837 European ancestry individuals NA Illumina [7724511] (imputed) 0 arachidoylcarnitine (C20) measurement http://www.ebi.ac.uk/efo/EFO_0800540 GCST90264825 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma argininate* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723750] (imputed) 3 argininate measurement http://www.ebi.ac.uk/efo/EFO_0800055 GCST90264826 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine argininate* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 3 argininate measurement http://www.ebi.ac.uk/efo/EFO_0800055 GCST90264827 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma arginine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90264828 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine arginine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723618] (imputed) 0 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90264829 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine argininosuccinate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723594] (imputed) 2 argininosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0010461 GCST90264830 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ascorbate (Vitamin C) levels in chronic kidney disease 2,955 European ancestry individuals NA Illumina [7722046] (imputed) 0 vitamin C measurement http://www.ebi.ac.uk/efo/EFO_0600003 GCST90264831 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ascorbic acid 2-sulfate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723857] (imputed) 1 ascorbic acid 2-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800169 GCST90264832 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ascorbic acid 3-sulfate* levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723651] (imputed) 1 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90264833 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ascorbic acid 3-sulfate* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90264834 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma asparagine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90264835 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine asparagine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90264836 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-hydroxymetoprolol levels in chronic kidney disease 423 European ancestry individuals NA Illumina [7721066] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264787 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-ketobutyrate levels in chronic kidney disease 4,752 European ancestry individuals NA Illumina [7723307] (imputed) 0 alpha-ketobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800140 GCST90264788 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-ketoglutaramate* levels in chronic kidney disease 4,919 European ancestry individuals NA Illumina [7723875] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264789 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-ketoglutaramate* levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7723846] (imputed) 0 alpha-ketoglutaramate measurement http://www.ebi.ac.uk/efo/EFO_0800046 GCST90264790 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-ketoglutarate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90264791 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-ketoglutarate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723526] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90264792 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-tocopherol levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90264793 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine amlodipine levels in chronic kidney disease 955 European ancestry individuals NA Illumina [7720093] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264794 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma andro steroid monosulfate C19H28O6S (1)* levels in chronic kidney disease 3,862 European ancestry individuals NA Illumina [7721491] (imputed) 1 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90264795 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine andro steroid monosulfate C19H28O6S (1)* levels in chronic kidney disease 4,455 European ancestry individuals NA Illumina [7724187] (imputed) 1 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90264796 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androstenediol (3alpha, 17alpha) monosulfate (2) levels in chronic kidney disease 4,014 European ancestry individuals NA Illumina [7722369] (imputed) 1 androstenediol (3alpha, 17alpha) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800292 GCST90264797 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androstenediol (3alpha, 17alpha) monosulfate (2) levels in chronic kidney disease 536 European ancestry individuals NA Illumina [7743641] (imputed) 0 androstenediol (3alpha, 17alpha) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800292 GCST90264798 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androstenediol (3alpha, 17alpha) monosulfate (3) levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724125] (imputed) 3 androstenediol (3alpha, 17alpha) monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0800293 GCST90264799 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androstenediol (3alpha, 17alpha) monosulfate (3) levels in chronic kidney disease 931 European ancestry individuals NA Illumina [7730548] (imputed) 0 androstenediol (3alpha, 17alpha) monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0800293 GCST90264800 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androstenediol (3beta,17beta) disulfate (1) levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723834] (imputed) 1 androstenediol (3beta,17beta) disulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800278 GCST90264801 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androstenediol (3beta,17beta) disulfate (1) levels in chronic kidney disease 4,776 European ancestry individuals NA Illumina [7723891] (imputed) 1 androstenediol (3beta,17beta) disulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800278 GCST90264802 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androstenediol (3beta,17beta) disulfate (2) levels in chronic kidney disease 4,948 European ancestry individuals NA Illumina [7724544] (imputed) 1 androstenediol (3beta,17beta) disulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800280 GCST90264803 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androstenediol (3beta,17beta) disulfate (2) levels in chronic kidney disease 4,842 European ancestry individuals NA Illumina [7724696] (imputed) 0 androstenediol (3beta,17beta) disulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800280 GCST90264804 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androstenediol (3beta,17beta) monosulfate (1) levels in chronic kidney disease 4,878 European ancestry individuals NA Illumina [7724064] (imputed) 1 androstenediol (3beta,17beta) monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800294 GCST90264805 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androstenediol (3beta,17beta) monosulfate (1) levels in chronic kidney disease 3,305 European ancestry individuals NA Illumina [7725275] (imputed) 0 androstenediol (3beta,17beta) monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800294 GCST90264806 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androstenediol (3beta,17beta) monosulfate (2) levels in chronic kidney disease 4,556 European ancestry individuals NA Illumina [7723857] (imputed) 0 androstenediol (3beta,17beta) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800295 GCST90264807 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androstenediol (3beta,17beta) monosulfate (2) levels in chronic kidney disease 733 European ancestry individuals NA Illumina [7735718] (imputed) 0 androstenediol (3beta,17beta) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800295 GCST90264808 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androsterone glucuronide levels in chronic kidney disease 4,738 European ancestry individuals NA Illumina [7724370] (imputed) 2 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90264809 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine androsterone glucuronide levels in chronic kidney disease 4,873 European ancestry individuals NA Illumina [7723750] (imputed) 1 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90264810 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma androsterone sulfate levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7723986] (imputed) 2 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90264811 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90265277 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723545] (imputed) 3 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90265278 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycitein glucuronide (2)* levels in chronic kidney disease 366 European ancestry individuals NA Illumina [7722656] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265279 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glyco-beta-muricholate** levels in chronic kidney disease 2,921 European ancestry individuals NA Illumina [7722347] (imputed) 1 glyco-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800569 GCST90265280 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glyco-beta-muricholate** levels in chronic kidney disease 4,179 European ancestry individuals NA Illumina [7724595] (imputed) 1 glyco-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800569 GCST90265281 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycochenodeoxycholate 3-sulfate levels in chronic kidney disease 4,710 European ancestry individuals NA Illumina [7723127] (imputed) 2 glycochenodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800384 GCST90265282 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycochenodeoxycholate 3-sulfate levels in chronic kidney disease 4,792 European ancestry individuals NA Illumina [7724283] (imputed) 2 glycochenodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800384 GCST90265283 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycochenodeoxycholate glucuronide (1) levels in chronic kidney disease 4,574 European ancestry individuals NA Illumina [7723668] (imputed) 1 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90265284 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycochenodeoxycholate glucuronide (1) levels in chronic kidney disease 4,109 European ancestry individuals NA Illumina [7723063] (imputed) 1 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90265285 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycochenodeoxycholate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90265286 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine betaine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264859 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine betonicine levels in chronic kidney disease 362 European ancestry individuals NA Illumina [7710783] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264860 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin (E,E)* levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7724061] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264861 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-CEHC glucuronide* levels in chronic kidney disease 4,889 European ancestry individuals NA Illumina [7724320] (imputed) 1 alpha-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800163 GCST90264775 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-CEHC glycine* levels in chronic kidney disease 2,532 European ancestry individuals NA Illumina [7724053] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264776 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-CEHC sulfate levels in chronic kidney disease 1,439 European ancestry individuals NA Illumina [7724384] (imputed) 0 alpha-CEHC sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800166 GCST90264777 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-CEHC sulfate levels in chronic kidney disease 4,859 European ancestry individuals NA Illumina [7723504] (imputed) 2 alpha-CEHC sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800166 GCST90264778 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-CEHC taurine* levels in chronic kidney disease 3,409 European ancestry individuals NA Illumina [7722712] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264779 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-CEHC levels in chronic kidney disease 637 European ancestry individuals NA Illumina [7733835] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264780 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-CMBHC glucuronide levels in chronic kidney disease 3,856 European ancestry individuals NA Illumina [7723307] (imputed) 0 alpha-CMBHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800167 GCST90264781 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-hydroxyisocaproate levels in chronic kidney disease 4,416 European ancestry individuals NA Illumina [7723225] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90264782 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-hydroxyisocaproate levels in chronic kidney disease 833 European ancestry individuals NA Illumina [7729026] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90264783 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-hydroxyisovalerate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 1 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90264784 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alpha-hydroxyisovalerate levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723593] (imputed) 1 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90264785 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alpha-hydroxymetoprolol levels in chronic kidney disease 861 European ancestry individuals NA Illumina [7716972] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264786 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 7-methylxanthine levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723625] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90264739 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 7,8-dihydroneopterin levels in chronic kidney disease 2,746 European ancestry individuals NA Illumina [7725129] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264740 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 8-methoxykynurenate levels in chronic kidney disease 3,910 European ancestry individuals NA Illumina [7722395] (imputed) 0 8-methoxykynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800096 GCST90264741 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 8-methoxykynurenate levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723559] (imputed) 0 8-methoxykynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800096 GCST90264742 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 9-hydroxystearate levels in chronic kidney disease 4,403 European ancestry individuals NA Illumina [7723021] (imputed) 0 9-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0800369 GCST90264743 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 9,10-DiHOME levels in chronic kidney disease 4,145 European ancestry individuals NA Illumina [7724988] (imputed) 0 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90264744 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine abscisate levels in chronic kidney disease 3,476 European ancestry individuals NA Illumina [7724037] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264745 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma acesulfame levels in chronic kidney disease 2,186 European ancestry individuals NA Illumina [7723316] (imputed) 0 acesulfame measurement http://www.ebi.ac.uk/efo/EFO_0801002 GCST90264746 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine acesulfame levels in chronic kidney disease 3,078 European ancestry individuals NA Illumina [7723356] (imputed) 0 acesulfame measurement http://www.ebi.ac.uk/efo/EFO_0801002 GCST90264747 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma acetylcarnitine (C2) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90264748 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine acetylcarnitine (C2) levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90264749 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine acetylsalicylate levels in chronic kidney disease 468 European ancestry individuals NA Illumina [7719108] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264750 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma acisoga levels in chronic kidney disease 4,763 European ancestry individuals NA Illumina [7723140] (imputed) 2 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90264751 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine acisoga levels in chronic kidney disease 4,877 European ancestry individuals NA Illumina [7723525] (imputed) 3 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90264752 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma aconitate [cis or trans] levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723875] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90264753 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine adenine levels in chronic kidney disease 4,729 European ancestry individuals NA Illumina [7723897] (imputed) 0 Adenine measurement http://www.ebi.ac.uk/efo/EFO_0021573 GCST90264754 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine adenosine 3',5'-cyclic monophosphate (cAMP) levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723622] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264755 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma adenosine 5'-monophosphate (AMP) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264756 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine adenosine levels in chronic kidney disease 4,861 European ancestry individuals NA Illumina [7723313] (imputed) 2 adenosine measurement http://www.ebi.ac.uk/efo/EFO_0010453 GCST90264757 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine adipate (C6-DC) levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723435] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264758 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma adipoylcarnitine (C6-DC) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 3 adipoylcarnitine (C6-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800380 GCST90264759 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine adipoylcarnitine (C6-DC) levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723517] (imputed) 3 adipoylcarnitine (C6-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800380 GCST90264760 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma adrenate (22:4n6) levels in chronic kidney disease 4,809 European ancestry individuals NA Illumina [7723761] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264761 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alanine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90264762 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alanine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90264763 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine of C7H12O2* levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723583] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265252 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glutamine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90265253 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90265254 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glutarate (C5-DC) levels in chronic kidney disease 4,821 European ancestry individuals NA Illumina [7723990] (imputed) 0 glutarate (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800620 GCST90265255 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutarate (C5-DC) levels in chronic kidney disease 4,816 European ancestry individuals NA Illumina [7722976] (imputed) 0 glutarate (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800620 GCST90265256 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glutarylcarnitine (C5-DC) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 5 glutarylcarnitine (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800030 GCST90265257 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutarylcarnitine (C5-DC) levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723620] (imputed) 4 glutarylcarnitine (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800030 GCST90265258 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycerate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90265259 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerate levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723496] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90265260 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycerol 3-phosphate levels in chronic kidney disease 3,644 European ancestry individuals NA Illumina [7724279] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90265261 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerol 3-phosphate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723603] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90265262 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycerol levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90265263 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerol levels in chronic kidney disease 3,107 European ancestry individuals NA Illumina [7721664] (imputed) 1 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90265264 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycerophosphoethanolamine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723877] (imputed) 0 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90265265 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerophosphoethanolamine levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723390] (imputed) 1 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90265266 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerophosphoglycerol levels in chronic kidney disease 4,886 European ancestry individuals NA Illumina [7724247] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265267 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerophosphoinositol* levels in chronic kidney disease 4,350 European ancestry individuals NA Illumina [7722989] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265268 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycerophosphorylcholine (GPC) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90265269 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerophosphorylcholine (GPC) levels in chronic kidney disease 4,613 European ancestry individuals NA Illumina [7723061] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90265270 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycerophosphoserine* levels in chronic kidney disease 4,873 European ancestry individuals NA Illumina [7723733] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265271 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycine conjugate of C10H12O2* levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724350] (imputed) 0 glycine conjugate of C10H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800654 GCST90265272 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycine conjugate of C10H14O2 (1)* levels in chronic kidney disease 4,763 European ancestry individuals NA Illumina [7723407] (imputed) 1 glycine conjugate of C10H14O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800655 GCST90265273 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycine conjugate of C10H14O2 (1)* levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724256] (imputed) 1 glycine conjugate of C10H14O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800655 GCST90265274 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycine conjugate of C6H10O2 (1)* levels in chronic kidney disease 4,649 European ancestry individuals NA Illumina [7725662] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265275 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycine conjugate of C9H16O2* levels in chronic kidney disease 4,679 European ancestry individuals NA Illumina [7724085] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265276 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C9H10O4 (1)* levels in chronic kidney disease 4,869 European ancestry individuals NA Illumina [7723989] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265227 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of piperine metabolite C17H21NO3 (1)* levels in chronic kidney disease 4,639 European ancestry individuals NA Illumina [7723122] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265228 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of piperine metabolite C17H21NO3 (2)* levels in chronic kidney disease 3,579 European ancestry individuals NA Illumina [7721787] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265229 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of piperine metabolite C17H21NO3 (3)* levels in chronic kidney disease 4,375 European ancestry individuals NA Illumina [7722343] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801031 GCST90265230 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of piperine metabolite C17H21NO3 (3)* levels in chronic kidney disease 4,747 European ancestry individuals NA Illumina [7724021] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801031 GCST90265231 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of piperine metabolite C17H21NO3 (4)* levels in chronic kidney disease 4,478 European ancestry individuals NA Illumina [7722738] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90265232 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of piperine metabolite C17H21NO3 (4)* levels in chronic kidney disease 4,851 European ancestry individuals NA Illumina [7723059] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90265233 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of piperine metabolite C17H21NO3 (5)* levels in chronic kidney disease 4,417 European ancestry individuals NA Illumina [7721954] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (5) measurement http://www.ebi.ac.uk/efo/EFO_0801033 GCST90265234 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of piperine metabolite C17H21NO3 (5)* levels in chronic kidney disease 4,783 European ancestry individuals NA Illumina [7723963] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (5) measurement http://www.ebi.ac.uk/efo/EFO_0801033 GCST90265235 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of piperine metabolite C17H21NO3 (6)* levels in chronic kidney disease 4,364 European ancestry individuals NA Illumina [7721276] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265236 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glutamate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90265237 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723545] (imputed) 1 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90265238 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C10H16O2 (2)* levels in chronic kidney disease 4,368 European ancestry individuals NA Illumina [7723785] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265239 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C6H10O2 (1)* (formerly X-12739) levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723592] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265240 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C6H10O2 (1)* (formerly X-24527) levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723528] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265241 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glutamine conjugate of C6H10O2 (1)* levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724705] (imputed) 0 glutamine conjugate of C6H10O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800657 GCST90265242 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glutamine conjugate of C6H10O2 (2)* levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723892] (imputed) 0 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90265243 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C6H10O2 (2)* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90265244 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glutamine conjugate of C7H12O2* levels in chronic kidney disease 4,748 European ancestry individuals NA Illumina [7724495] (imputed) 0 glutamine conjugate of C7H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800656 GCST90265245 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C8H12O2 (1)* levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723628] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265246 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C8H12O2 (2)* levels in chronic kidney disease 4,832 European ancestry individuals NA Illumina [7723808] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265247 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C8H12O2 (3)* levels in chronic kidney disease 4,665 European ancestry individuals NA Illumina [7722837] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265248 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C8H12O4 (1)* levels in chronic kidney disease 4,837 European ancestry individuals NA Illumina [7724223] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265249 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C8H12O4 (2)* levels in chronic kidney disease 3,517 European ancestry individuals NA Illumina [7721790] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265250 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glutamine conjugate of C9H16O2 (1)* levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723601] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265251 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2,N5-diacetylornithine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723523] (imputed) 1 N2,N5-diacetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800070 GCST90265694 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2,N6-diacetyllysine levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723493] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265695 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N3-methyluridine levels in chronic kidney disease 4,861 European ancestry individuals NA Illumina [7723478] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265696 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N4-acetylcytidine levels in chronic kidney disease 4,522 European ancestry individuals NA Illumina [7723695] (imputed) 0 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90265697 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N4-acetylcytidine levels in chronic kidney disease 4,882 European ancestry individuals NA Illumina [7724428] (imputed) 0 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90265698 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N4-acetylsulfamethoxazole* levels in chronic kidney disease 427 European ancestry individuals NA Illumina [7734771] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265699 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N6-acetyllysine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90265700 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6-acetyllysine levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724476] (imputed) 3 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90265701 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6-carbamoylthreonyladenosine levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723687] (imputed) 0 N6-carbamoylthreonyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800629 GCST90265702 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6-carboxyethyllysine levels in chronic kidney disease 4,721 European ancestry individuals NA Illumina [7723812] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265703 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6-carboxymethyllysine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 N6-carboxymethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800146 GCST90265704 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N6-methyladenosine levels in chronic kidney disease 4,057 European ancestry individuals NA Illumina [7724161] (imputed) 0 N6-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800639 GCST90265705 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6-methyladenosine levels in chronic kidney disease 1,920 European ancestry individuals NA Illumina [7723223] (imputed) 0 N6-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800639 GCST90265706 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N6-methyllysine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90265707 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6-methyllysine levels in chronic kidney disease 4,811 European ancestry individuals NA Illumina [7723107] (imputed) 2 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90265708 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6-succinyladenosine levels in chronic kidney disease 4,705 European ancestry individuals NA Illumina [7723846] (imputed) 0 N6-succinyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021428 GCST90265709 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N6,N6-dimethyllysine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90265710 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6,N6-dimethyllysine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90265711 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N6,N6,N6-trimethyllysine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90265712 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N6,N6,N6-trimethyllysine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723630] (imputed) 1 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90265713 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine naringenin 7-glucuronide levels in chronic kidney disease 3,475 European ancestry individuals NA Illumina [7724840] (imputed) 0 naringenin 7-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801015 GCST90265714 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine naringenin levels in chronic kidney disease 1,240 European ancestry individuals NA Illumina [7729651] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265715 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine neopterin levels in chronic kidney disease 4,826 European ancestry individuals NA Illumina [7724061] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265716 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma nervonoylcarnitine (C24:1)* levels in chronic kidney disease 4,625 European ancestry individuals NA Illumina [7723915] (imputed) 2 nervonoylcarnitine (C24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800549 GCST90265717 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nicotinamide N-oxide levels in chronic kidney disease 4,263 European ancestry individuals NA Illumina [7723517] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265718 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N,N-dimethylalanine levels in chronic kidney disease 4,935 European ancestry individuals NA Illumina [7724665] (imputed) 0 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90265669 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N,N-dimethylalanine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723518] (imputed) 0 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90265670 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N,N,N-trimethyl-5-aminovalerate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90265671 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N,N,N-trimethyl-5-aminovalerate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90265672 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N,N,N-trimethyl-alanylproline betaine (TMAP) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723827] (imputed) 1 N,N,N-trimethyl-alanylproline betaine (TMAP) measurement http://www.ebi.ac.uk/efo/EFO_0800094 GCST90265673 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N,N,N-trimethyl-alanylproline betaine (TMAP) levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723613] (imputed) 1 N,N,N-trimethyl-alanylproline betaine (TMAP) measurement http://www.ebi.ac.uk/efo/EFO_0800094 GCST90265674 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N('1)-acetylspermidine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723861] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265675 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N1-Methyl-2-pyridone-5-carboxamide levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90265676 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N1-Methyl-2-pyridone-5-carboxamide levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90265677 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N1-methyladenosine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723906] (imputed) 0 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90265678 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N1-methyladenosine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723609] (imputed) 0 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90265679 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N1-methylguanosine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723608] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265680 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N1-methylinosine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723805] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90265681 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N1-methylinosine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723656] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90265682 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N1,N12-diacetylspermine levels in chronic kidney disease 4,422 European ancestry individuals NA Illumina [7724342] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265683 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N2-acetyl,N6-methyllysine levels in chronic kidney disease 4,943 European ancestry individuals NA Illumina [7724550] (imputed) 2 N2-acetyl,N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800109 GCST90265684 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2-acetyl,N6-methyllysine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723613] (imputed) 2 N2-acetyl,N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800109 GCST90265685 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N2-acetyl,N6,N6-dimethyllysine levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723765] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265686 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2-acetyl,N6,N6-dimethyllysine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265687 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2-acetyllysine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723486] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265688 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2-methylguanosine levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723784] (imputed) 1 N2-methylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0800634 GCST90265689 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2,N2-dimethylguanine levels in chronic kidney disease 3,515 European ancestry individuals NA Illumina [7723090] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90265690 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N2,N2-dimethylguanosine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90265691 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N2,N2-dimethylguanosine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 3 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90265692 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N2,N5-diacetylornithine levels in chronic kidney disease 4,460 European ancestry individuals NA Illumina [7724423] (imputed) 1 N2,N5-diacetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800070 GCST90265693 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma nicotinamide levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724689] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90265719 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nicotinamide ribonucleotide (NMN) levels in chronic kidney disease 714 European ancestry individuals NA Illumina [7717902] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265720 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nicotinamide riboside levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723510] (imputed) 1 nicotinamide riboside measurement http://www.ebi.ac.uk/efo/EFO_0800156 GCST90265721 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nicotinamide levels in chronic kidney disease 4,898 European ancestry individuals NA Illumina [7724430] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90265722 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nicotinate ribonucleoside levels in chronic kidney disease 3,818 European ancestry individuals NA Illumina [7722068] (imputed) 0 nicotinate ribonucleoside measurement http://www.ebi.ac.uk/efo/EFO_0800157 GCST90265723 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nicotine levels in chronic kidney disease 2,544 European ancestry individuals NA Illumina [7725335] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265724 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nicotinurate (nicotinoylglycine) levels in chronic kidney disease 3,449 European ancestry individuals NA Illumina [7725468] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265725 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma nisinate (24:6n3) levels in chronic kidney disease 2,660 European ancestry individuals NA Illumina [7721406] (imputed) 0 nisinate (24:6n3) measurement http://www.ebi.ac.uk/efo/EFO_0800536 GCST90265726 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma nonadecanoate (19:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90265727 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma nonadecenamide (19:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265728 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma nonanoylcarnitine (C9) levels in chronic kidney disease 4,686 European ancestry individuals NA Illumina [7723975] (imputed) 2 nonanoylcarnitine (C9) measurement http://www.ebi.ac.uk/efo/EFO_0800381 GCST90265729 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nonenedioate (C9:1-DC)* levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723823] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265730 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma norcotinine levels in chronic kidney disease 498 European ancestry individuals NA Illumina [7747421] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265731 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine nornicotine levels in chronic kidney disease 805 European ancestry individuals NA Illumina [7724931] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265732 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma o-cresol sulfate levels in chronic kidney disease 4,806 European ancestry individuals NA Illumina [7723400] (imputed) 0 O-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800955 GCST90265733 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine o-cresol sulfate levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723596] (imputed) 0 O-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800955 GCST90265734 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma O-sulfo-L-tyrosine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265735 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine O-sulfo-L-tyrosine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265736 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma octadecadienedioate (C18:2-DC)* levels in chronic kidney disease 4,930 European ancestry individuals NA Illumina [7724286] (imputed) 1 octadecadienedioate (C18:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800565 GCST90265737 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma octadecanedioate (C18-DC) levels in chronic kidney disease 4,932 European ancestry individuals NA Illumina [7724105] (imputed) 1 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90265738 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma octadecanedioylcarnitine (C18-DC)* levels in chronic kidney disease 4,776 European ancestry individuals NA Illumina [7724459] (imputed) 2 octadecanedioylcarnitine (C18-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800371 GCST90265739 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma octadecenedioate (C18:1-DC) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723831] (imputed) 1 octadecenedioate (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800563 GCST90265740 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma octadecenedioylcarnitine (C18:1-DC)* levels in chronic kidney disease 4,900 European ancestry individuals NA Illumina [7724695] (imputed) 1 octadecenedioylcarnitine (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800370 GCST90265741 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma octanoylcarnitine (C8) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90265742 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine octanoylcarnitine (C8) levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723588] (imputed) 1 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90265743 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma p-cresol glucuronide* levels in chronic kidney disease 4,626 European ancestry individuals NA Illumina [7722899] (imputed) 0 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90265769 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine p-cresol glucuronide* levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723612] (imputed) 0 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90265770 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma p-cresol sulfate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90265771 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine p-cresol sulfate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90265772 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitamide (16:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265773 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitate (16:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90265774 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoleamide (16:1)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265775 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoleate (16:1n7) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90265776 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoleoyl-linoleoyl-glycerol (16:1/18:2) [1]* levels in chronic kidney disease 4,487 European ancestry individuals NA Illumina [7723791] (imputed) 0 palmitoleoyl-linoleoyl-glycerol (16:1/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800504 GCST90265777 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoleoylcarnitine (C16:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 palmitoleoylcarnitine (C16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800493 GCST90265778 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoloelycholine levels in chronic kidney disease 2,589 European ancestry individuals NA Illumina [7723893] (imputed) 0 palmitoloelycholine measurement http://www.ebi.ac.uk/efo/EFO_0800480 GCST90265779 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl dihydrosphingomyelin (d18:0/16:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 palmitoyl dihydrosphingomyelin (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800400 GCST90265780 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl ethanolamide levels in chronic kidney disease 4,924 European ancestry individuals NA Illumina [7724213] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265781 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl sphingomyelin (d18:1/16:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90265782 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine palmitoyl sphingomyelin (d18:1/16:0) levels in chronic kidney disease 3,727 European ancestry individuals NA Illumina [7723407] (imputed) 0 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90265783 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl-arachidonoyl-glycerol (16:0/20:4) [2]* levels in chronic kidney disease 2,553 European ancestry individuals NA Illumina [7724129] (imputed) 0 Palmitoyl-arachidonoyl-glycerol (16:0/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0022103 GCST90265784 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl-linoleoyl-glycerol (16:0/18:2) [1]* levels in chronic kidney disease 4,043 European ancestry individuals NA Illumina [7725696] (imputed) 0 palmitoyl-linoleoyl-glycerol (16:0/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800435 GCST90265785 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl-linoleoyl-glycerol (16:0/18:2) [2]* levels in chronic kidney disease 4,230 European ancestry individuals NA Illumina [7724494] (imputed) 0 palmitoyl-linoleoyl-glycerol (16:0/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800438 GCST90265786 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl-oleoyl-glycerol (16:0/18:1) [1]* levels in chronic kidney disease 2,629 European ancestry individuals NA Illumina [7723001] (imputed) 0 palmitoyl-oleoyl-glycerol (16:0/18:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800495 GCST90265787 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl-oleoyl-glycerol (16:0/18:1) [2]* levels in chronic kidney disease 3,520 European ancestry individuals NA Illumina [7724390] (imputed) 0 palmitoyl-oleoyl-glycerol (16:0/18:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800496 GCST90265788 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800591 GCST90265789 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoylcarnitine (C16) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90265790 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma palmitoylcholine levels in chronic kidney disease 4,927 European ancestry individuals NA Illumina [7724005] (imputed) 0 palmitoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800473 GCST90265791 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pantoate levels in chronic kidney disease 3,383 European ancestry individuals NA Illumina [7724846] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265792 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pantoate levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723362] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265793 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tryptophan betaine levels in chronic kidney disease 4,939 European ancestry individuals NA Illumina [7724846] (imputed) 1 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90266101 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ursodeoxycholate levels in chronic kidney disease 4,332 European ancestry individuals NA Illumina [7724179] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90266127 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tryptophan levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90266103 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma valine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723663] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90266129 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tyramine O-sulfate levels in chronic kidney disease 4,422 European ancestry individuals NA Illumina [7723209] (imputed) 0 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90266105 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma valsartan levels in chronic kidney disease 628 European ancestry individuals NA Illumina [7724619] (imputed) 0 valsartan measurement http://www.ebi.ac.uk/efo/EFO_0801224 GCST90266131 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine valsartan levels in chronic kidney disease 609 European ancestry individuals NA Illumina [7716149] (imputed) 0 valsartan measurement http://www.ebi.ac.uk/efo/EFO_0801224 GCST90266132 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma valylglycine levels in chronic kidney disease 4,298 European ancestry individuals NA Illumina [7724052] (imputed) 0 valylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800680 GCST90266133 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine valylleucine levels in chronic kidney disease 3,029 European ancestry individuals NA Illumina [7722687] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266134 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma umbelliferone sulfate levels in chronic kidney disease 3,596 European ancestry individuals NA Illumina [7724164] (imputed) 0 umbelliferone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801006 GCST90266110 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine umbelliferone sulfate levels in chronic kidney disease 4,879 European ancestry individuals NA Illumina [7724174] (imputed) 0 umbelliferone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801006 GCST90266111 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma undecanedioate (C11-DC) levels in chronic kidney disease 3,180 European ancestry individuals NA Illumina [7724090] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266112 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma vanillate glucuronide levels in chronic kidney disease 2,717 European ancestry individuals NA Illumina [7721002] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266137 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine undecenoylcarnitine (C11:1) levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7724148] (imputed) 1 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90266114 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma vanillic acid glycine levels in chronic kidney disease 4,681 European ancestry individuals NA Illumina [7724006] (imputed) 0 vanillic acid glycine measurement http://www.ebi.ac.uk/efo/EFO_0801056 GCST90266139 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine uracil levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723620] (imputed) 0 uracil measurement http://www.ebi.ac.uk/efo/EFO_0800644 GCST90266116 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma vanillic alcohol sulfate levels in chronic kidney disease 3,325 European ancestry individuals NA Illumina [7721940] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266141 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine vanillic alcohol sulfate levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724592] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266142 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma urea levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90266119 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine vanillylmandelate (VMA) levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90266144 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine uric acid ribonucleoside* levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723842] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266121 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma uridine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90266122 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine uridine levels in chronic kidney disease 4,876 European ancestry individuals NA Illumina [7724055] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90266123 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine urocortisol glucuronide (4) levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723627] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266124 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-10445 levels in chronic kidney disease 3,805 European ancestry individuals NA Illumina [7724612] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266148 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-10457 levels in chronic kidney disease 4,824 European ancestry individuals NA Illumina [7723682] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266149 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-10458 levels in chronic kidney disease 4,082 European ancestry individuals NA Illumina [7724701] (imputed) 0 X-10458 measurement http://www.ebi.ac.uk/efo/EFO_0800692 GCST90266150 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleamide levels in chronic kidney disease 4,941 European ancestry individuals NA Illumina [7724715] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265744 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleate/vaccenate (18:1) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265745 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoyl ethanolamide levels in chronic kidney disease 4,772 European ancestry individuals NA Illumina [7724076] (imputed) 1 oleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800604 GCST90265746 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoyl-arachidonoyl-glycerol (18:1/20:4) [1]* levels in chronic kidney disease 4,682 European ancestry individuals NA Illumina [7724548] (imputed) 2 oleoyl-arachidonoyl-glycerol (18:1/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800507 GCST90265747 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoyl-arachidonoyl-glycerol (18:1/20:4) [2]* levels in chronic kidney disease 4,585 European ancestry individuals NA Illumina [7725067] (imputed) 2 oleoyl-arachidonoyl-glycerol (18:1/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800508 GCST90265748 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoyl-linoleoyl-glycerol (18:1/18:2) [1] levels in chronic kidney disease 4,929 European ancestry individuals NA Illumina [7724403] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265749 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoyl-linoleoyl-glycerol (18:1/18:2) [2] levels in chronic kidney disease 4,936 European ancestry individuals NA Illumina [7724527] (imputed) 1 oleoyl-linoleoyl-glycerol (18:1/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800333 GCST90265750 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoyl-oleoyl-glycerol (18:1/18:1) [1]* levels in chronic kidney disease 4,271 European ancestry individuals NA Illumina [7723717] (imputed) 1 oleoyl-oleoyl-glycerol (18:1/18:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800497 GCST90265751 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoyl-oleoyl-glycerol (18:1/18:1) [2]* levels in chronic kidney disease 4,696 European ancestry individuals NA Illumina [7724922] (imputed) 1 oleoyl-oleoyl-glycerol (18:1/18:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800498 GCST90265752 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoylcarnitine (C18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90265753 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oleoylcholine levels in chronic kidney disease 4,878 European ancestry individuals NA Illumina [7723652] (imputed) 0 oleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800477 GCST90265754 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma omeprazole levels in chronic kidney disease 459 European ancestry individuals NA Illumina [7715501] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265755 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine orcinol sulfate levels in chronic kidney disease 4,561 European ancestry individuals NA Illumina [7724623] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265756 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ornithine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90265757 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ornithine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723630] (imputed) 1 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90265758 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma orotate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723663] (imputed) 1 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90265759 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine orotate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723499] (imputed) 0 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90265760 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma orotidine levels in chronic kidney disease 4,944 European ancestry individuals NA Illumina [7724393] (imputed) 1 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90265761 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine orotidine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 2 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90265762 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oxalate (ethanedioate) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265763 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine oxalate (ethanedioate) levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265764 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oxindolylalanine levels in chronic kidney disease 4,945 European ancestry individuals NA Illumina [7724652] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265765 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine oxindolylalanine levels in chronic kidney disease 4,819 European ancestry individuals NA Illumina [7723869] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265766 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma oxypurinol levels in chronic kidney disease 3,159 European ancestry individuals NA Illumina [7721568] (imputed) 0 oxypurinol measurement http://www.ebi.ac.uk/efo/EFO_0801213 GCST90265767 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine oxypurinol levels in chronic kidney disease 2,045 European ancestry individuals NA Illumina [7723722] (imputed) 0 oxypurinol measurement http://www.ebi.ac.uk/efo/EFO_0801213 GCST90265768 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pantoprazole levels in chronic kidney disease 689 European ancestry individuals NA Illumina [7730145] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265794 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pantothenate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90265795 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pantothenate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723614] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90265796 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma paraxanthine levels in chronic kidney disease 4,671 European ancestry individuals NA Illumina [7724220] (imputed) 0 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90265797 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine paraxanthine levels in chronic kidney disease 4,362 European ancestry individuals NA Illumina [7725232] (imputed) 0 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90265798 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pelargonate (9:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 pelargonate 9:0 measurement http://www.ebi.ac.uk/efo/EFO_0021106 GCST90265799 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pentadecanamide (15:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265800 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pentadecanoate (15:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 pentadecanoate 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021073 GCST90265801 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pentose acid* levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7723858] (imputed) 0 pentose acid measurement http://www.ebi.ac.uk/efo/EFO_0800660 GCST90265802 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma perfluorooctanesulfonate (PFOS) levels in chronic kidney disease 4,919 European ancestry individuals NA Illumina [7723513] (imputed) 0 perfluorooctanesulfonate (PFOS) measurement http://www.ebi.ac.uk/efo/EFO_0801018 GCST90265803 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma perfluorooctanoate (PFOA) levels in chronic kidney disease 4,701 European ancestry individuals NA Illumina [7723420] (imputed) 0 perfluorooctanoate (PFOA) measurement http://www.ebi.ac.uk/efo/EFO_0801024 GCST90265804 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trans-aconitate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266087 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma trans-urocanate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723782] (imputed) 1 trans-urocanate measurement http://www.ebi.ac.uk/efo/EFO_0800138 GCST90266088 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trans-urocanate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723615] (imputed) 1 trans-urocanate measurement http://www.ebi.ac.uk/efo/EFO_0800138 GCST90266089 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine triacetate lactone levels in chronic kidney disease 4,715 European ancestry individuals NA Illumina [7723901] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266090 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tricarballylate levels in chronic kidney disease 3,989 European ancestry individuals NA Illumina [7723873] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266091 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tricosanoyl sphingomyelin (d18:1/23:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 tricosanoyl sphingomyelin (d18:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0800401 GCST90266092 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tridecenedioate (C13:1-DC)* levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7724168] (imputed) 1 tridecenedioate (C13:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800309 GCST90266093 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine triethanolamine levels in chronic kidney disease 4,686 European ancestry individuals NA Illumina [7724167] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266094 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma trigonelline (N'-methylnicotinate) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90266095 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trigonelline (N'-methylnicotinate) levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723545] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90266096 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma trimethylamine N-oxide levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90266097 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trimethylamine N-oxide levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90266098 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trizma acetate levels in chronic kidney disease 3,502 European ancestry individuals NA Illumina [7723103] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266099 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tryptamine levels in chronic kidney disease 3,853 European ancestry individuals NA Illumina [7724026] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266100 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ursocholate levels in chronic kidney disease 2,756 European ancestry individuals NA Illumina [7721487] (imputed) 0 ursocholate measurement http://www.ebi.ac.uk/efo/EFO_0800328 GCST90266126 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tryptophan betaine levels in chronic kidney disease 4,198 European ancestry individuals NA Illumina [7724251] (imputed) 0 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90266102 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine valine betaine levels in chronic kidney disease 3,764 European ancestry individuals NA Illumina [7722142] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266128 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tryptophan levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723638] (imputed) 2 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90266104 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine valine levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723679] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90266130 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tyramine O-sulfate levels in chronic kidney disease 4,899 European ancestry individuals NA Illumina [7724125] (imputed) 0 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90266106 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tyramine levels in chronic kidney disease 4,438 European ancestry individuals NA Illumina [7724904] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266107 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tyrosine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90266108 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tyrosine levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723381] (imputed) 2 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90266109 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma vanillactate levels in chronic kidney disease 4,546 European ancestry individuals NA Illumina [7723424] (imputed) 0 vanillactate measurement http://www.ebi.ac.uk/efo/EFO_0800078 GCST90266135 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine vanillactate levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724290] (imputed) 0 vanillactate measurement http://www.ebi.ac.uk/efo/EFO_0800078 GCST90266136 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma undecenoylcarnitine (C11:1) levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723808] (imputed) 2 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90266113 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine vanillate levels in chronic kidney disease 4,307 European ancestry individuals NA Illumina [7723180] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266138 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma uracil levels in chronic kidney disease 4,128 European ancestry individuals NA Illumina [7723724] (imputed) 0 uracil measurement http://www.ebi.ac.uk/efo/EFO_0800644 GCST90266115 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine vanillic acid glycine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 vanillic acid glycine measurement http://www.ebi.ac.uk/efo/EFO_0801056 GCST90266140 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma urate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90266117 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine urate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90266118 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma vanillylmandelate (VMA) levels in chronic kidney disease 4,852 European ancestry individuals NA Illumina [7723502] (imputed) 0 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90266143 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine urea levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723619] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90266120 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma veratric acid levels in chronic kidney disease 2,679 European ancestry individuals NA Illumina [7721525] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266145 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-07765 levels in chronic kidney disease 4,373 European ancestry individuals NA Illumina [7723510] (imputed) 0 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90266146 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-07765 levels in chronic kidney disease 3,792 European ancestry individuals NA Illumina [7723828] (imputed) 0 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90266147 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine Urolithin A levels in chronic kidney disease 1,355 European ancestry individuals NA Illumina [7722231] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266125 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-10458 levels in chronic kidney disease 4,295 European ancestry individuals NA Illumina [7725784] (imputed) 0 X-10458 measurement http://www.ebi.ac.uk/efo/EFO_0800692 GCST90266151 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11299 levels in chronic kidney disease 4,830 European ancestry individuals NA Illumina [7723521] (imputed) 0 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90266152 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11299 levels in chronic kidney disease 3,242 European ancestry individuals NA Illumina [7722079] (imputed) 0 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90266153 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11308 levels in chronic kidney disease 4,917 European ancestry individuals NA Illumina [7723939] (imputed) 1 X-11308 measurement http://www.ebi.ac.uk/efo/EFO_0800693 GCST90266154 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11315 levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7724097] (imputed) 0 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90266155 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11372 levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724501] (imputed) 0 X-11372 measurement http://www.ebi.ac.uk/efo/EFO_0800694 GCST90266156 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11381 levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723724] (imputed) 2 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90266157 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11407 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266158 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11444 levels in chronic kidney disease 4,894 European ancestry individuals NA Illumina [7724681] (imputed) 1 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90266159 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11444 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723445] (imputed) 0 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90266160 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11470 levels in chronic kidney disease 4,745 European ancestry individuals NA Illumina [7724527] (imputed) 2 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90266161 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11470 levels in chronic kidney disease 4,853 European ancestry individuals NA Illumina [7723879] (imputed) 2 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90266162 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11478 levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724447] (imputed) 1 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90266163 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11483 levels in chronic kidney disease 3,615 European ancestry individuals NA Illumina [7720933] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90266164 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11612 levels in chronic kidney disease 4,715 European ancestry individuals NA Illumina [7723440] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266165 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11632 levels in chronic kidney disease 3,859 European ancestry individuals NA Illumina [7722510] (imputed) 0 X-11632 measurement http://www.ebi.ac.uk/efo/EFO_0800697 GCST90266166 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11787 levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723848] (imputed) 2 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90266167 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11787 levels in chronic kidney disease 4,700 European ancestry individuals NA Illumina [7723816] (imputed) 0 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90266168 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11795 levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723831] (imputed) 0 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90266169 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11795 levels in chronic kidney disease 3,684 European ancestry individuals NA Illumina [7723781] (imputed) 0 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90266170 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11843 levels in chronic kidney disease 4,259 European ancestry individuals NA Illumina [7721560] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90266171 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11843 levels in chronic kidney disease 4,900 European ancestry individuals NA Illumina [7724284] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90266172 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11847 levels in chronic kidney disease 3,614 European ancestry individuals NA Illumina [7723396] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90266173 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11847 levels in chronic kidney disease 1,914 European ancestry individuals NA Illumina [7725678] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90266174 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11849 levels in chronic kidney disease 3,795 European ancestry individuals NA Illumina [7725133] (imputed) 1 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90266175 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12283 levels in chronic kidney disease 4,656 European ancestry individuals NA Illumina [7723395] (imputed) 0 X-12283 measurement http://www.ebi.ac.uk/efo/EFO_0800713 GCST90266226 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12283 levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723341] (imputed) 0 X-12283 measurement http://www.ebi.ac.uk/efo/EFO_0800713 GCST90266227 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12306 levels in chronic kidney disease 2,729 European ancestry individuals NA Illumina [7723358] (imputed) 0 X-12306 measurement http://www.ebi.ac.uk/efo/EFO_0800714 GCST90266228 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12306 levels in chronic kidney disease 4,822 European ancestry individuals NA Illumina [7724023] (imputed) 0 X-12306 measurement http://www.ebi.ac.uk/efo/EFO_0800714 GCST90266229 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12379 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266230 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12407 levels in chronic kidney disease 4,706 European ancestry individuals NA Illumina [7723898] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90266231 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12407 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723447] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90266232 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12410 levels in chronic kidney disease 4,285 European ancestry individuals NA Illumina [7723702] (imputed) 1 X-12410 measurement http://www.ebi.ac.uk/efo/EFO_0800715 GCST90266233 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12410 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723630] (imputed) 1 X-12410 measurement http://www.ebi.ac.uk/efo/EFO_0800715 GCST90266234 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12411 levels in chronic kidney disease 4,894 European ancestry individuals NA Illumina [7724422] (imputed) 1 X-12411 measurement http://www.ebi.ac.uk/efo/EFO_0800716 GCST90266235 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12411 levels in chronic kidney disease 4,893 European ancestry individuals NA Illumina [7724716] (imputed) 1 X-12411 measurement http://www.ebi.ac.uk/efo/EFO_0800716 GCST90266236 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12456 levels in chronic kidney disease 3,214 European ancestry individuals NA Illumina [7722834] (imputed) 1 X-12456 measurement http://www.ebi.ac.uk/efo/EFO_0021311 GCST90266237 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12462 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 X-12462 measurement http://www.ebi.ac.uk/efo/EFO_0800717 GCST90266238 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12543 levels in chronic kidney disease 3,297 European ancestry individuals NA Illumina [7723532] (imputed) 0 X-12543 measurement http://www.ebi.ac.uk/efo/EFO_0800718 GCST90266239 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12543 levels in chronic kidney disease 4,867 European ancestry individuals NA Illumina [7724057] (imputed) 0 X-12543 measurement http://www.ebi.ac.uk/efo/EFO_0800718 GCST90266240 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12544 levels in chronic kidney disease 4,811 European ancestry individuals NA Illumina [7723328] (imputed) 0 X-12544 measurement http://www.ebi.ac.uk/efo/EFO_0021315 GCST90266241 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12680 levels in chronic kidney disease 4,934 European ancestry individuals NA Illumina [7724430] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90266242 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12680 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90266243 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12687 levels in chronic kidney disease 4,869 European ancestry individuals NA Illumina [7723422] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266244 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12689 levels in chronic kidney disease 4,645 European ancestry individuals NA Illumina [7724234] (imputed) 1 X-12689 measurement http://www.ebi.ac.uk/efo/EFO_0800719 GCST90266245 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12701 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723593] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266246 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12704 levels in chronic kidney disease 4,249 European ancestry individuals NA Illumina [7724944] (imputed) 1 X-12704 measurement http://www.ebi.ac.uk/efo/EFO_0021322 GCST90266247 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12706 levels in chronic kidney disease 4,877 European ancestry individuals NA Illumina [7724269] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266248 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12707 levels in chronic kidney disease 4,886 European ancestry individuals NA Illumina [7724385] (imputed) 2 X-12707 measurement http://www.ebi.ac.uk/efo/EFO_0800720 GCST90266249 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12708 levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723574] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266250 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12111 levels in chronic kidney disease 2,820 European ancestry individuals NA Illumina [7722960] (imputed) 0 X-12111 measurement http://www.ebi.ac.uk/efo/EFO_0800704 GCST90266201 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12111 levels in chronic kidney disease 4,868 European ancestry individuals NA Illumina [7723255] (imputed) 0 X-12111 measurement http://www.ebi.ac.uk/efo/EFO_0800704 GCST90266202 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12112 levels in chronic kidney disease 4,863 European ancestry individuals NA Illumina [7723766] (imputed) 2 X-12112 measurement http://www.ebi.ac.uk/efo/EFO_0800705 GCST90266203 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12112 levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7724356] (imputed) 2 X-12112 measurement http://www.ebi.ac.uk/efo/EFO_0800705 GCST90266204 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12117 levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723836] (imputed) 1 X-12117 measurement http://www.ebi.ac.uk/efo/EFO_0800706 GCST90266205 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12117 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723659] (imputed) 1 X-12117 measurement http://www.ebi.ac.uk/efo/EFO_0800706 GCST90266206 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12124 levels in chronic kidney disease 4,638 European ancestry individuals NA Illumina [7723685] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266207 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12125 levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723806] (imputed) 2 X-12125 measurement http://www.ebi.ac.uk/efo/EFO_0800707 GCST90266208 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12126 levels in chronic kidney disease 2,742 European ancestry individuals NA Illumina [7722494] (imputed) 0 X-12126 measurement http://www.ebi.ac.uk/efo/EFO_0800708 GCST90266209 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12126 levels in chronic kidney disease 4,891 European ancestry individuals NA Illumina [7724532] (imputed) 1 X-12126 measurement http://www.ebi.ac.uk/efo/EFO_0800708 GCST90266210 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12127 levels in chronic kidney disease 2,983 European ancestry individuals NA Illumina [7721796] (imputed) 0 X-12127 measurement http://www.ebi.ac.uk/efo/EFO_0800709 GCST90266211 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12127 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-12127 measurement http://www.ebi.ac.uk/efo/EFO_0800709 GCST90266212 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12193 levels in chronic kidney disease 3,616 European ancestry individuals NA Illumina [7722169] (imputed) 0 X-12193 measurement http://www.ebi.ac.uk/efo/EFO_0800710 GCST90266213 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12193 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 X-12193 measurement http://www.ebi.ac.uk/efo/EFO_0800710 GCST90266214 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12199 levels in chronic kidney disease 3,986 European ancestry individuals NA Illumina [7723164] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266215 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12199 levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723525] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266216 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12214 levels in chronic kidney disease 4,488 European ancestry individuals NA Illumina [7724630] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266217 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12216 levels in chronic kidney disease 4,797 European ancestry individuals NA Illumina [7723810] (imputed) 1 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90266218 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12216 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723631] (imputed) 0 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90266219 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12221 levels in chronic kidney disease 4,573 European ancestry individuals NA Illumina [7724208] (imputed) 0 X-12221 measurement http://www.ebi.ac.uk/efo/EFO_0800711 GCST90266220 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12221 levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723755] (imputed) 0 X-12221 measurement http://www.ebi.ac.uk/efo/EFO_0800711 GCST90266221 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12261 levels in chronic kidney disease 2,544 European ancestry individuals NA Illumina [7724948] (imputed) 0 X-12261 measurement http://www.ebi.ac.uk/efo/EFO_0021301 GCST90266222 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12261 levels in chronic kidney disease 4,851 European ancestry individuals NA Illumina [7724091] (imputed) 0 X-12261 measurement http://www.ebi.ac.uk/efo/EFO_0021301 GCST90266223 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12262 levels in chronic kidney disease 3,771 European ancestry individuals NA Illumina [7721992] (imputed) 0 X-12262 measurement http://www.ebi.ac.uk/efo/EFO_0800712 GCST90266224 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12267 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266225 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11849 levels in chronic kidney disease 1,303 European ancestry individuals NA Illumina [7725011] (imputed) 0 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90266176 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11850 levels in chronic kidney disease 4,630 European ancestry individuals NA Illumina [7723601] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90266177 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11850 levels in chronic kidney disease 4,818 European ancestry individuals NA Illumina [7723535] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90266178 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11852 levels in chronic kidney disease 4,703 European ancestry individuals NA Illumina [7723786] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90266179 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11852 levels in chronic kidney disease 4,645 European ancestry individuals NA Illumina [7724182] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90266180 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11858 levels in chronic kidney disease 2,253 European ancestry individuals NA Illumina [7724149] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90266181 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11858 levels in chronic kidney disease 1,578 European ancestry individuals NA Illumina [7727224] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90266182 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-11880 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723433] (imputed) 0 X-11880 measurement http://www.ebi.ac.uk/efo/EFO_0800698 GCST90266183 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-11979 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723631] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266184 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12007 levels in chronic kidney disease 4,882 European ancestry individuals NA Illumina [7724034] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90266185 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12007 levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723607] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90266186 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12013 levels in chronic kidney disease 2,662 European ancestry individuals NA Illumina [7722130] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90266187 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12013 levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723410] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90266188 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12015 levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724561] (imputed) 0 X-12015 measurement http://www.ebi.ac.uk/efo/EFO_0800699 GCST90266189 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12026 levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723280] (imputed) 0 X-12026 measurement http://www.ebi.ac.uk/efo/EFO_0800700 GCST90266190 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12026 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723659] (imputed) 0 X-12026 measurement http://www.ebi.ac.uk/efo/EFO_0800700 GCST90266191 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12027 levels in chronic kidney disease 4,531 European ancestry individuals NA Illumina [7724291] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266192 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12096 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723601] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266193 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12097 levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724317] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266194 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12100 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 X-12100 measurement http://www.ebi.ac.uk/efo/EFO_0800701 GCST90266195 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12100 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 X-12100 measurement http://www.ebi.ac.uk/efo/EFO_0800701 GCST90266196 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12101 levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724101] (imputed) 0 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90266197 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12101 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723606] (imputed) 0 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90266198 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12104 levels in chronic kidney disease 4,337 European ancestry individuals NA Illumina [7723687] (imputed) 0 X-12104 measurement http://www.ebi.ac.uk/efo/EFO_0800703 GCST90266199 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12104 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-12104 measurement http://www.ebi.ac.uk/efo/EFO_0800703 GCST90266200 Genome-wide genotyping array 2023-06-01 36710296 Tsai MC 2023-01-30 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36710296 Genome-wide association study of age at menarche in the Taiwan Biobank suggests NOL4 as a novel associated gene. Age at menarche 39,827 individuals NA Affymetrix [494552] 4 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90270114 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Colorectal cancer (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90013862 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Asthma (Firth correction) 401,847 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90013888 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Coronary artery disease (Firth correction) 352,063 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90013864 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Glaucoma (Firth correction) 406,927 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90013865 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Colorectal cancer (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90013866 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Thyroid cancer (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90013867 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Coronary artery disease (SPA correction) 352,063 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90013868 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Glaucoma (SPA correction) 406,927 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90013869 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Guillain-Barré syndrome (Firth correction) 406,298 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Guillain-Barre syndrome http://www.ebi.ac.uk/efo/EFO_0007292 GCST90013894 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Miserableness (UKB data field 1930) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 feeling miserable measurement http://www.ebi.ac.uk/efo/EFO_0009598 GCST90013874 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Irritability (UKB data field 1940) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90013875 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Bell's palsy (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Bell's palsy http://www.ebi.ac.uk/efo/EFO_0007167 GCST90013876 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Spinal cord disorder (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 spinal cord disease http://www.ebi.ac.uk/efo/EFO_0009488 GCST90013877 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Depression (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90013878 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Sjogren's syndrome (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90013879 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Clotting disorder excessive bleeding (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 blood coagulation disease http://www.ebi.ac.uk/efo/EFO_0009314 GCST90013880 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Osteoarthritis (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90013881 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. High cholesterol (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90013882 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Inflammatory bowel disease (Firth correction) 404,781 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90013901 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Psoriasis (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90013885 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Angina (Firth correction) 397,554 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90013886 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cystitis (Firth correction) 381,591 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90013903 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Retinitis pigmentosa (Firth correction) 403,833 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0019200 GCST90013904 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Macular degeneration (Firth correction) 403,837 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90013905 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cellulitis (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90013906 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Guilty feelings (UKB data field 2030) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 guilt measurement http://www.ebi.ac.uk/efo/EFO_0009595 GCST90013907 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Risk taking (UKB data field 2040) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90013908 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Seen doctor for nerves anxiety tension or depression (UKB data field 2090) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 seeing a general practitioner for nerves, anxiety, tension or depression, self-reported http://www.ebi.ac.uk/efo/EFO_0009820 GCST90013909 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Seen psychiatrist for nerves anxiety tension or depression (UKB data field 2100) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 seeing a psychiatrist for nerves, anxiety, tension or depression, self-reported http://www.ebi.ac.uk/efo/EFO_0009821 GCST90013910 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Hearing difficulty problems (UKB data field 2247) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90013911 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Pulmonary embolism (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90013937 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Fractured bones in last 5 years (UKB data field 2463) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90013913 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cholelithiasis gall stones (SPA correction) 404,405 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cholelithiasis, gallstones http://www.ebi.ac.uk/efo/EFO_0004799, http://www.ebi.ac.uk/efo/EFO_0004210 GCST90013939 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Urinary tract infection or kidney infection (SPA correction) 397,867 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90013940 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Type 1 diabetes (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90013941 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Type 2 diabetes (SPA correction) 406,831 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90013942 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Hypothyroidism or myxoedema (SPA correction) 405,357 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 myxedema, hypothyroidism http://www.ebi.ac.uk/efo/EFO_1001055, http://www.ebi.ac.uk/efo/EFO_0004705 GCST90013943 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Guillain-Barré syndrome (SPA correction) 406,298 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Guillain-Barre syndrome http://www.ebi.ac.uk/efo/EFO_0007292 GCST90013944 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Epilepsy (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90013945 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Depression (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90013928 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Sjogren's syndrome (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90013929 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Clotting disorder or excessive bleeding (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 blood coagulation disease http://www.ebi.ac.uk/efo/EFO_0009314 GCST90013930 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Osteoarthritis (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90013931 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. High cholesterol (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90013932 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. goiter (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 goiter http://www.ebi.ac.uk/efo/EFO_0004283 GCST90013933 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Insomnia (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90013934 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Guilty feelings (UKB data field 2030) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 guilt measurement http://www.ebi.ac.uk/efo/EFO_0009595 GCST90013957 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Risk taking (UKB data field 2040) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90013958 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Seen doctor for nerves anxiety tension or depression (UKB data field 2090) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 seeing a general practitioner for nerves, anxiety, tension or depression, self-reported http://www.ebi.ac.uk/efo/EFO_0009820 GCST90013959 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Seen psychiatrist for nerves anxiety tension or depression (UKB data field 2100) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 seeing a psychiatrist for nerves, anxiety, tension or depression, self-reported http://www.ebi.ac.uk/efo/EFO_0009821 GCST90013960 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Hearing difficulty problems (UKB data field 2247) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90013961 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Pulmonary embolism (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90013887 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Thyroid cancer (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90013863 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cholelithiasis gall stones (Firth correction) 404,405 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cholelithiasis, gallstones http://www.ebi.ac.uk/efo/EFO_0004799, http://www.ebi.ac.uk/efo/EFO_0004210 GCST90013889 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Urinary tract infection or kidney infection (Firth correction) 397,867 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90013890 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Type 1 diabetes (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90013891 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Type 2 diabetes (Firth correction) 406,831 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90013892 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Hypothyroidism or myxoedema (Firth correction) 405,357 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 myxedema, hypothyroidism http://www.ebi.ac.uk/efo/EFO_1001055, http://www.ebi.ac.uk/efo/EFO_0004705 GCST90013893 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Body mass index (UKB data field 21001) 407,609 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90013870 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Direct low density lipoprotein levels (UKB data field 30780) 389,189 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90013871 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Total bilirubin levels (UKB data field 30840) 388,303 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90013872 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Mood swings (UKB data field 1920) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST90013873 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Epilepsy (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90013895 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Retinal detachment (Firth correction) 403,643 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90013896 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Back problem (Firth correction) 402,528 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Abnormality of the cervical spine http://purl.obolibrary.org/obo/HP_0003319 GCST90013897 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Muscle or soft tissue problem (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90013898 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Allergy hypersensitivity anaphylaxis (Firth correction) 407,498 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90013899 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Bronchitis (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bronchitis http://www.ebi.ac.uk/efo/EFO_0009661 GCST90013900 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. goiter (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 goiter http://www.ebi.ac.uk/efo/EFO_0004283 GCST90013883 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Insomnia (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90013884 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Atrial fibrillation (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90013902 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Chest pain or discomfort (UKB data field 2335) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90013912 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Asthma (SPA correction) 401,847 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90013938 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Reason for glasses/contact lenses: short-sightedness (UKB data field 6147_1) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90013914 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cataract (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90013915 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. High blood pressure (UKB data field 6150) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Increased blood pressure http://purl.obolibrary.org/obo/HP_0032263 GCST90013916 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Pain type(s) experienced in last month: Headache (UKB data field 6159_1) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90013917 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Pain type(s) experienced in last month: Hip pain (UKB data field 6159_6) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90013918 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cholesterol lowering medication use (UKB data field 6177_1) (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90013919 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Allergic rhinitis (Firth correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90013920 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Any parental history of Alzheimer's disease (Firth correction) 407,089 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90013921 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Any parental history of lung cancer (Firth correction) 407,521 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0006953 GCST90013922 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Mood swings (UKB data field 1920) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST90013923 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Miserableness (UKB data field 1930) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 feeling miserable measurement http://www.ebi.ac.uk/efo/EFO_0009598 GCST90013924 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Irritability (UKB data field 1940) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90013925 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Bell's palsy (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Bell's palsy http://www.ebi.ac.uk/efo/EFO_0007167 GCST90013926 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Spinal cord disorder (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 spinal cord disease http://www.ebi.ac.uk/efo/EFO_0009488 GCST90013927 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Retinal detachment (SPA correction) 403,643 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90013946 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Back problem (SPA correction) 402,528 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Abnormality of the cervical spine http://purl.obolibrary.org/obo/HP_0003319 GCST90013947 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Muscle or soft tissue problem (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90013948 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Allergy hypersensitivity anaphylaxis (SPA correction) 407,498 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90013949 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Bronchitis (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bronchitis http://www.ebi.ac.uk/efo/EFO_0009661 GCST90013950 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Inflammatory bowel disease (SPA correction) 404,781 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90013951 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Atrial fibrillation (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90013952 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cystitis (SPA correction) 381,591 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90013953 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Retinitis pigmentosa (SPA correction) 403,833 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0019200 GCST90013954 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Macular degeneration (SPA correction) 403,837 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90013955 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cellulitis (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90013956 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Psoriasis (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90013935 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Angina (SPA correction) 397,554 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90013936 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2'-O-methyluridine levels in chronic kidney disease 4,350 European ancestry individuals NA Illumina [7724200] (imputed) 1 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90264439 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2'-O-methyluridine levels in chronic kidney disease 3,855 European ancestry individuals NA Illumina [7723620] (imputed) 2 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90264440 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 21-hydroxypregnenolone disulfate levels in chronic kidney disease 4,789 European ancestry individuals NA Illumina [7724383] (imputed) 1 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90264441 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 21-hydroxypregnenolone disulfate levels in chronic kidney disease 4,838 European ancestry individuals NA Illumina [7724452] (imputed) 1 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90264442 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2R,3R-dihydroxybutyrate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 1 2R,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800314 GCST90264443 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2S,3R-dihydroxybutyrate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723853] (imputed) 1 2s,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800312 GCST90264444 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-(3-amino-3-carboxypropyl)uridine* levels in chronic kidney disease 4,374 European ancestry individuals NA Illumina [7723286] (imputed) 0 3-(3-amino-3-carboxypropyl)uridine measurement http://www.ebi.ac.uk/efo/EFO_0800632 GCST90264445 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-(3-amino-3-carboxypropyl)uridine* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 3-(3-amino-3-carboxypropyl)uridine measurement http://www.ebi.ac.uk/efo/EFO_0800632 GCST90264446 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-(3-hydroxyphenyl)propionate levels in chronic kidney disease 3,793 European ancestry individuals NA Illumina [7724519] (imputed) 0 3-(3-hydroxyphenyl)propionate measurement http://www.ebi.ac.uk/efo/EFO_0800952 GCST90264447 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-(3-hydroxyphenyl)propionate sulfate levels in chronic kidney disease 3,325 European ancestry individuals NA Illumina [7723517] (imputed) 0 3-(3-hydroxyphenyl)propionate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800990 GCST90264448 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-(3-hydroxyphenyl)propionate sulfate levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7723606] (imputed) 0 3-(3-hydroxyphenyl)propionate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800990 GCST90264449 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-(3-hydroxyphenyl)propionate levels in chronic kidney disease 4,309 European ancestry individuals NA Illumina [7723953] (imputed) 1 3-(3-hydroxyphenyl)propionate measurement http://www.ebi.ac.uk/efo/EFO_0800952 GCST90264450 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-(4-hydroxyphenyl)lactate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723549] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264451 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-(4-hydroxyphenyl)lactate levels in chronic kidney disease 4,830 European ancestry individuals NA Illumina [7724373] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264452 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-(cystein-S-yl)acetaminophen* levels in chronic kidney disease 815 European ancestry individuals NA Illumina [7723865] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264453 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-(methylthio)acetaminophen sulfate* levels in chronic kidney disease 371 European ancestry individuals NA Illumina [7728721] (imputed) 0 3-(methylthio)acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801045 GCST90264454 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-(methylthio)acetaminophen sulfate* levels in chronic kidney disease 1,163 European ancestry individuals NA Illumina [7724499] (imputed) 0 3-(methylthio)acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801045 GCST90264455 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-(N-acetyl-L-cystein-S-yl) acetaminophen levels in chronic kidney disease 1,281 European ancestry individuals NA Illumina [7728896] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264456 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-acetylphenol sulfate levels in chronic kidney disease 4,576 European ancestry individuals NA Illumina [7723639] (imputed) 0 3-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800983 GCST90264457 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-acetylphenol sulfate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723641] (imputed) 0 3-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800983 GCST90264458 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-acetylphenol levels in chronic kidney disease 2,763 European ancestry individuals NA Illumina [7723058] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264459 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-amino-2-piperidone levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90264460 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-amino-2-piperidone levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90264461 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-aminoisobutyrate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723850] (imputed) 2 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90264462 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-aminoisobutyrate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723561] (imputed) 2 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90264463 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-bromo-5-chloro-2,6-dihydroxybenzoic acid* levels in chronic kidney disease 3,022 European ancestry individuals NA Illumina [7722193] (imputed) 1 3-bromo-5-chloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801058 GCST90264464 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP)** levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264465 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP)** levels in chronic kidney disease 4,817 European ancestry individuals NA Illumina [7724003] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264466 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (CMPF) levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7724035] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264467 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (CMPF) levels in chronic kidney disease 4,604 European ancestry individuals NA Illumina [7724184] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264468 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-decenoylcarnitine levels in chronic kidney disease 3,686 European ancestry individuals NA Illumina [7723619] (imputed) 1 3-decenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800589 GCST90264469 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-ethylcatechol sulfate (1) levels in chronic kidney disease 4,568 European ancestry individuals NA Illumina [7723204] (imputed) 0 3-ethylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801047 GCST90264470 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-ethylcatechol sulfate (1) levels in chronic kidney disease 4,726 European ancestry individuals NA Illumina [7723549] (imputed) 0 3-ethylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801047 GCST90264471 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-ethylcatechol sulfate (2) levels in chronic kidney disease 3,263 European ancestry individuals NA Illumina [7722571] (imputed) 0 3-ethylcatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801048 GCST90264472 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-ethylcatechol sulfate (2) levels in chronic kidney disease 4,353 European ancestry individuals NA Illumina [7722775] (imputed) 0 3-ethylcatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801048 GCST90264473 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-ethylphenylsulfate levels in chronic kidney disease 3,316 European ancestry individuals NA Illumina [7721535] (imputed) 0 3-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0800956 GCST90264474 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-formylindole levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723669] (imputed) 2 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90264475 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-formylindole levels in chronic kidney disease 4,838 European ancestry individuals NA Illumina [7724861] (imputed) 2 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90264476 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxy-2-ethylpropionate levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723689] (imputed) 0 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90264477 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxy-2-ethylpropionate levels in chronic kidney disease 4,811 European ancestry individuals NA Illumina [7723544] (imputed) 0 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90264478 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxy-2-methylpyridine sulfate levels in chronic kidney disease 4,629 European ancestry individuals NA Illumina [7724179] (imputed) 0 3-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801052 GCST90264479 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxy-2-methylpyridine sulfate levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723531] (imputed) 0 3-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801052 GCST90264480 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxy-3-methylglutarate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723663] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90264481 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxy-3-methylglutarate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723463] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90264482 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyadipate levels in chronic kidney disease 4,570 European ancestry individuals NA Illumina [7722884] (imputed) 1 3-hydroxyadipate measurement http://www.ebi.ac.uk/efo/EFO_0800351 GCST90264483 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyadipate levels in chronic kidney disease 4,898 European ancestry individuals NA Illumina [7724518] (imputed) 0 3-hydroxyadipate measurement http://www.ebi.ac.uk/efo/EFO_0800351 GCST90264484 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyanthranilate levels in chronic kidney disease 4,697 European ancestry individuals NA Illumina [7724722] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264485 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxybutyrate (BHBA) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264486 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxybutyrate (BHBA) levels in chronic kidney disease 4,007 European ancestry individuals NA Illumina [7723814] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264487 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxybutyroylglycine** levels in chronic kidney disease 4,678 European ancestry individuals NA Illumina [7724106] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264488 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxybutyroylglycine** levels in chronic kidney disease 407 European ancestry individuals NA Illumina [7709391] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264489 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxycinnamate sulfate levels in chronic kidney disease 4,764 European ancestry individuals NA Illumina [7724116] (imputed) 1 3-hydroxycinnamate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800994 GCST90264490 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxycinnamate levels in chronic kidney disease 2,867 European ancestry individuals NA Illumina [7722373] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264491 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxycotinine glucuronide levels in chronic kidney disease 773 European ancestry individuals NA Illumina [7730309] (imputed) 0 3-hydroxycotinine glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800984 GCST90264492 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxycotinine glucuronide levels in chronic kidney disease 1,007 European ancestry individuals NA Illumina [7726703] (imputed) 0 3-hydroxycotinine glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800984 GCST90264493 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxydecanoate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 3-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800198 GCST90264494 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxydecanoylcarnitine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 3-hydroxydecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800590 GCST90264495 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxydodecanedioate* levels in chronic kidney disease 3,632 European ancestry individuals NA Illumina [7721982] (imputed) 0 3-hydroxydodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0800226 GCST90264496 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxydodecanedioate* levels in chronic kidney disease 4,656 European ancestry individuals NA Illumina [7723425] (imputed) 1 3-hydroxydodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0800226 GCST90264497 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyhexanoate levels in chronic kidney disease 4,592 European ancestry individuals NA Illumina [7724240] (imputed) 1 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90264498 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyhexanoate levels in chronic kidney disease 3,230 European ancestry individuals NA Illumina [7724161] (imputed) 0 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90264499 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyhexanoylcarnitine (1) levels in chronic kidney disease 4,937 European ancestry individuals NA Illumina [7724454] (imputed) 0 3-hydroxyhexanoylcarnitine (1) measurement http://www.ebi.ac.uk/efo/EFO_0800580 GCST90264500 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyhexanoylcarnitine (1) levels in chronic kidney disease 4,860 European ancestry individuals NA Illumina [7723370] (imputed) 0 3-hydroxyhexanoylcarnitine (1) measurement http://www.ebi.ac.uk/efo/EFO_0800580 GCST90264501 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyhexanoylcarnitine (2) levels in chronic kidney disease 3,612 European ancestry individuals NA Illumina [7722935] (imputed) 0 3-hydroxyhexanoylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800581 GCST90264502 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyhippurate levels in chronic kidney disease 4,933 European ancestry individuals NA Illumina [7724438] (imputed) 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90264503 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyhippurate sulfate levels in chronic kidney disease 3,721 European ancestry individuals NA Illumina [7723354] (imputed) 0 3-hydroxyhippurate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801030 GCST90264504 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyhippurate sulfate levels in chronic kidney disease 4,871 European ancestry individuals NA Illumina [7723966] (imputed) 0 3-hydroxyhippurate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801030 GCST90264505 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyhippurate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90264506 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyindolin-2-one levels in chronic kidney disease 3,687 European ancestry individuals NA Illumina [7723322] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264507 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyindolin-2-one sulfate levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724510] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264508 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyindolin-2-one levels in chronic kidney disease 4,202 European ancestry individuals NA Illumina [7723504] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264509 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyisobutyrate levels in chronic kidney disease 4,933 European ancestry individuals NA Illumina [7724372] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90264510 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyisobutyrate levels in chronic kidney disease 4,888 European ancestry individuals NA Illumina [7724248] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90264511 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxykynurenine levels in chronic kidney disease 4,555 European ancestry individuals NA Illumina [7724017] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264512 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxylaurate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723888] (imputed) 1 3-hydroxylaurate measurement http://www.ebi.ac.uk/efo/EFO_0800204 GCST90264513 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-indoxyl sulfate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 3-indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022088 GCST90264539 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-indoxyl sulfate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 3-indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022088 GCST90264540 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methoxycatechol sulfate (1) levels in chronic kidney disease 4,856 European ancestry individuals NA Illumina [7723846] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90264541 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methoxycatechol sulfate (1) levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724339] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90264542 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methoxycatechol sulfate (2) levels in chronic kidney disease 4,786 European ancestry individuals NA Illumina [7724166] (imputed) 0 3-methoxycatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801010 GCST90264543 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methoxytyramine sulfate levels in chronic kidney disease 2,691 European ancestry individuals NA Illumina [7725311] (imputed) 0 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90264544 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methoxytyramine sulfate levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7724306] (imputed) 0 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90264545 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methoxytyramine levels in chronic kidney disease 4,225 European ancestry individuals NA Illumina [7725160] (imputed) 0 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90264546 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methoxytyrosine levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7723948] (imputed) 0 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90264547 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methoxytyrosine levels in chronic kidney disease 4,724 European ancestry individuals NA Illumina [7724464] (imputed) 0 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90264548 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methyl catechol sulfate (1) levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724535] (imputed) 0 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90264549 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methyl catechol sulfate (1) levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723735] (imputed) 0 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90264550 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methyl catechol sulfate (2) levels in chronic kidney disease 3,990 European ancestry individuals NA Illumina [7724068] (imputed) 0 3-methyl catechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800973 GCST90264551 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methyl catechol sulfate (2) levels in chronic kidney disease 4,839 European ancestry individuals NA Illumina [7724130] (imputed) 0 3-methyl catechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800973 GCST90264552 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methyl-2-oxobutyrate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723796] (imputed) 0 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90264553 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methyl-2-oxobutyrate levels in chronic kidney disease 4,442 European ancestry individuals NA Illumina [7724517] (imputed) 0 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90264554 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methyl-2-oxovalerate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723731] (imputed) 0 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90264555 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methyl-2-oxovalerate levels in chronic kidney disease 4,293 European ancestry individuals NA Illumina [7725377] (imputed) 0 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90264556 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methyladipate levels in chronic kidney disease 4,287 European ancestry individuals NA Illumina [7723826] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90264557 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methyladipate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723574] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90264558 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methylcrotonylglycine levels in chronic kidney disease 4,192 European ancestry individuals NA Illumina [7724156] (imputed) 1 monocyte chemotactic protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008235 GCST90264559 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylcrotonylglycine levels in chronic kidney disease 4,876 European ancestry individuals NA Illumina [7723989] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264560 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylcytidine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723583] (imputed) 2 3-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800633 GCST90264561 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methylglutaconate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723663] (imputed) 2 3-methylglutaconate measurement http://www.ebi.ac.uk/efo/EFO_0800047 GCST90264562 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylglutaconate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 2 3-methylglutaconate measurement http://www.ebi.ac.uk/efo/EFO_0800047 GCST90264563 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine theophylline levels in chronic kidney disease 4,480 European ancestry individuals NA Illumina [7725656] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90266064 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine thiamin (Vitamin B1) levels in chronic kidney disease 4,180 European ancestry individuals NA Illumina [7724619] (imputed) 0 thiamine measurement http://www.ebi.ac.uk/efo/EFO_0010540 GCST90266065 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma thioproline levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90266066 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine thioproline levels in chronic kidney disease 4,819 European ancestry individuals NA Illumina [7724270] (imputed) 0 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90266067 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma threonate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90266068 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine threonate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723661] (imputed) 0 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90266069 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma threonine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90266070 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine threonine levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723641] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90266071 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine thymine levels in chronic kidney disease 4,237 European ancestry individuals NA Illumina [7724343] (imputed) 1 thymine measurement http://www.ebi.ac.uk/efo/EFO_0800646 GCST90266072 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma thymol sulfate levels in chronic kidney disease 4,780 European ancestry individuals NA Illumina [7724041] (imputed) 1 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90266073 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine thymol sulfate levels in chronic kidney disease 4,813 European ancestry individuals NA Illumina [7724017] (imputed) 0 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90266074 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma thyroxine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723699] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90266075 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tigloylglycine levels in chronic kidney disease 2,058 European ancestry individuals NA Illumina [7721741] (imputed) 1 tigloylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800121 GCST90266076 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tigloylglycine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 tigloylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800121 GCST90266077 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tiglylcarnitine (C5:1-DC) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723793] (imputed) 0 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90266078 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tiglylcarnitine (C5:1-DC) levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723569] (imputed) 0 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90266079 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma torasemide levels in chronic kidney disease 1,432 European ancestry individuals NA Illumina [7724384] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266080 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma trans-2-hexenoylglycine levels in chronic kidney disease 1,972 European ancestry individuals NA Illumina [7721818] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266081 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trans-2-hexenoylglycine levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723646] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266082 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trans-3,4-methyleneheptanoylcarnitine levels in chronic kidney disease 2,112 European ancestry individuals NA Illumina [7722597] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266083 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trans-3,4-methyleneheptanoylglycine levels in chronic kidney disease 4,501 European ancestry individuals NA Illumina [7723735] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266084 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma trans-4-hydroxyproline levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90266085 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine trans-4-hydroxyproline levels in chronic kidney disease 4,336 European ancestry individuals NA Illumina [7724225] (imputed) 0 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90266086 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2'-O-methylcytidine levels in chronic kidney disease 4,947 European ancestry individuals NA Illumina [7724782] (imputed) 1 2'-O-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800635 GCST90264437 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2'-O-methylcytidine levels in chronic kidney disease 4,899 European ancestry individuals NA Illumina [7724577] (imputed) 1 2'-O-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800635 GCST90264438 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxymyristate levels in chronic kidney disease 4,920 European ancestry individuals NA Illumina [7723972] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264514 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyoctanoate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723844] (imputed) 0 3-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800193 GCST90264515 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyoctanoyl glycine levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724594] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264516 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyoctanoylcarnitine (1) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723841] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264517 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyoctanoylcarnitine (1) levels in chronic kidney disease 4,878 European ancestry individuals NA Illumina [7724210] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264518 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyoctanoylcarnitine (2) levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724752] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264519 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyoctanoylcarnitine (2) levels in chronic kidney disease 4,195 European ancestry individuals NA Illumina [7724340] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264520 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyoleoylcarnitine levels in chronic kidney disease 3,791 European ancestry individuals NA Illumina [7723252] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264521 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyphenylacetate sulfate levels in chronic kidney disease 4,856 European ancestry individuals NA Illumina [7723431] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264522 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyphenylacetate levels in chronic kidney disease 4,888 European ancestry individuals NA Illumina [7724730] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264523 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyphenylacetoylcarnitine levels in chronic kidney disease 4,173 European ancestry individuals NA Illumina [7723263] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264524 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxyphenylacetoylglutamine levels in chronic kidney disease 3,664 European ancestry individuals NA Illumina [7723229] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264525 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxyphenylacetoylglutamine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723616] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264526 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxypropanoate levels in chronic kidney disease 499 European ancestry individuals NA Illumina [7740208] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264527 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxypyridine glucuronide levels in chronic kidney disease 4,082 European ancestry individuals NA Illumina [7723952] (imputed) 0 3-hydroxypyridine glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801043 GCST90264528 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxypyridine glucuronide levels in chronic kidney disease 4,844 European ancestry individuals NA Illumina [7724438] (imputed) 0 3-hydroxypyridine glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801043 GCST90264529 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxypyridine sulfate levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723789] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90264530 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxypyridine sulfate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90264531 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxysebacate levels in chronic kidney disease 3,311 European ancestry individuals NA Illumina [7721974] (imputed) 0 3-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800205 GCST90264532 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxysebacate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723593] (imputed) 2 3-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800205 GCST90264533 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-hydroxystachydrine* levels in chronic kidney disease 4,564 European ancestry individuals NA Illumina [7723278] (imputed) 0 3-hydroxystachydrine measurement http://www.ebi.ac.uk/efo/EFO_0801022 GCST90264534 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxystachydrine* levels in chronic kidney disease 381 European ancestry individuals NA Illumina [7738305] (imputed) 0 3-hydroxystachydrine measurement http://www.ebi.ac.uk/efo/EFO_0801022 GCST90264535 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-hydroxysuberate levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724432] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264536 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-indoleglyoxylic acid levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723602] (imputed) 2 3-indoleglyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801027 GCST90264537 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-indoleglyoxylic acid levels in chronic kidney disease 4,274 European ancestry individuals NA Illumina [7723873] (imputed) 0 3-indoleglyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801027 GCST90264538 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methylpipecolate levels in chronic kidney disease 4,371 European ancestry individuals NA Illumina [7723471] (imputed) 1 N-methylpipecolate measurement http://www.ebi.ac.uk/efo/EFO_0800988 GCST90265644 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-methylproline levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90265645 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methylproline levels in chronic kidney disease 4,899 European ancestry individuals NA Illumina [7724263] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90265646 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-methyltaurine levels in chronic kidney disease 3,245 European ancestry individuals NA Illumina [7726016] (imputed) 0 N-methyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800064 GCST90265647 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methyltaurine levels in chronic kidney disease 4,408 European ancestry individuals NA Illumina [7724042] (imputed) 0 N-methyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800064 GCST90265648 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-nervonoyl-sphingadiene (d18:2/24:1)* levels in chronic kidney disease 4,701 European ancestry individuals NA Illumina [7723819] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265649 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-octanoylglutamine levels in chronic kidney disease 4,696 European ancestry individuals NA Illumina [7725590] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265650 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-octanoylglycine levels in chronic kidney disease 1,129 European ancestry individuals NA Illumina [7722940] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265651 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-oleoylserine levels in chronic kidney disease 4,617 European ancestry individuals NA Illumina [7723057] (imputed) 1 N-oleoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800525 GCST90265652 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-oleoyltaurine levels in chronic kidney disease 3,985 European ancestry individuals NA Illumina [7723901] (imputed) 1 N-oleoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800337 GCST90265653 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-palmitoyl-heptadecasphingosine (d17:1/16:0)* levels in chronic kidney disease 4,215 European ancestry individuals NA Illumina [7723042] (imputed) 1 N-palmitoyl-heptadecasphingosine (d17:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800531 GCST90265654 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-palmitoyl-sphingadienine (d18:2/16:0)* levels in chronic kidney disease 4,763 European ancestry individuals NA Illumina [7723744] (imputed) 0 N-palmitoyl-sphingadienine (d18:2/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800516 GCST90265655 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-palmitoyl-sphinganine (d18:0/16:0) levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724610] (imputed) 1 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90265656 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-palmitoyl-sphingosine (d18:1/16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90265657 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-palmitoylglycine levels in chronic kidney disease 4,918 European ancestry individuals NA Illumina [7723661] (imputed) 2 N-palmitoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800342 GCST90265658 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-palmitoylserine levels in chronic kidney disease 4,536 European ancestry individuals NA Illumina [7724129] (imputed) 0 N-palmitoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800524 GCST90265659 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-palmitoyltaurine levels in chronic kidney disease 2,184 European ancestry individuals NA Illumina [7721299] (imputed) 0 N-palmitoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800339 GCST90265660 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-stearoyl-sphingadienine (d18:2/18:0)* levels in chronic kidney disease 3,644 European ancestry individuals NA Illumina [7725227] (imputed) 1 N-stearoyl-sphingadienine (d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800521 GCST90265661 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-stearoyl-sphingosine (d18:1/18:0)* levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723853] (imputed) 2 N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800613 GCST90265662 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-stearoylserine* levels in chronic kidney disease 2,607 European ancestry individuals NA Illumina [7722085] (imputed) 0 N-stearoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800559 GCST90265663 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-stearoyltaurine levels in chronic kidney disease 2,370 European ancestry individuals NA Illumina [7721196] (imputed) 0 N-stearoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800340 GCST90265664 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N,N-dimethyl-5-aminovalerate levels in chronic kidney disease 3,617 European ancestry individuals NA Illumina [7723384] (imputed) 0 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90265665 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N,N-dimethyl-5-aminovalerate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723428] (imputed) 3 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90265666 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N,N-dimethyl-pro-pro levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265667 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N,N-dimethyl-pro-pro levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723870] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265668 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine myo-inositol levels in chronic kidney disease 1,618 European ancestry individuals NA Illumina [7721062] (imputed) 1 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90265519 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myristamide (14:0)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265520 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myristate (14:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90265521 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myristoleamide (14:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265522 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myristoleate (14:1n5) levels in chronic kidney disease 4,941 European ancestry individuals NA Illumina [7724844] (imputed) 0 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90265523 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myristoleoylcarnitine (C14:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90265524 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine myristoleoylcarnitine (C14:1)* levels in chronic kidney disease 3,983 European ancestry individuals NA Illumina [7724164] (imputed) 0 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90265525 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myristoyl dihydrosphingomyelin (d18:0/14:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 myristoyl dihydrosphingomyelin (d18:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800433 GCST90265526 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myristoylcarnitine (C14) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723812] (imputed) 0 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90265527 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-(2-furoyl)glycine levels in chronic kidney disease 4,876 European ancestry individuals NA Illumina [7724081] (imputed) 0 N-(2-furoyl)glycine measurement http://www.ebi.ac.uk/efo/EFO_0800947 GCST90265528 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-(2-furoyl)glycine levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723543] (imputed) 0 N-(2-furoyl)glycine measurement http://www.ebi.ac.uk/efo/EFO_0800947 GCST90265529 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyl-1-methylhistidine* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723864] (imputed) 1 N-acetyl-1-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800065 GCST90265530 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-1-methylhistidine* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 N-acetyl-1-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800065 GCST90265531 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyl-2-aminooctanoate* levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723808] (imputed) 1 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90265532 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-2-aminooctanoate* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90265533 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyl-3-methylhistidine* levels in chronic kidney disease 4,496 European ancestry individuals NA Illumina [7724351] (imputed) 1 N-acetyl-3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800044 GCST90265534 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-3-methylhistidine* levels in chronic kidney disease 4,893 European ancestry individuals NA Illumina [7724138] (imputed) 1 N-acetyl-3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800044 GCST90265535 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyl-aspartyl-glutamate (NAAG) levels in chronic kidney disease 4,071 European ancestry individuals NA Illumina [7723087] (imputed) 3 N-acetyl-aspartyl-glutamate (NAAG) measurement http://www.ebi.ac.uk/efo/EFO_0800033 GCST90265536 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-aspartyl-glutamate (NAAG) levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723532] (imputed) 2 N-acetyl-aspartyl-glutamate (NAAG) measurement http://www.ebi.ac.uk/efo/EFO_0800033 GCST90265537 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyl-beta-alanine levels in chronic kidney disease 4,948 European ancestry individuals NA Illumina [7724591] (imputed) 1 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90265538 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-beta-alanine levels in chronic kidney disease 4,870 European ancestry individuals NA Illumina [7723873] (imputed) 1 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90265539 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-lactoyl leucine levels in chronic kidney disease 4,705 European ancestry individuals NA Illumina [7723376] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265628 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyl-cadaverine levels in chronic kidney disease 3,145 European ancestry individuals NA Illumina [7724102] (imputed) 0 N-acetyl-cadaverine measurement http://www.ebi.ac.uk/efo/EFO_0800045 GCST90265540 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-cadaverine levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724671] (imputed) 1 N-acetyl-cadaverine measurement http://www.ebi.ac.uk/efo/EFO_0800045 GCST90265541 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyl-isoputreanine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 3 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90265542 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylglutamate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723795] (imputed) 0 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90265568 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylglutamate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723496] (imputed) 1 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90265569 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylglutamine levels in chronic kidney disease 4,822 European ancestry individuals NA Illumina [7723709] (imputed) 1 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90265570 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylglutamine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723607] (imputed) 1 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90265571 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylglycine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90265572 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylglycine levels in chronic kidney disease 4,387 European ancestry individuals NA Illumina [7724657] (imputed) 0 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90265573 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylhistamine levels in chronic kidney disease 650 European ancestry individuals NA Illumina [7728972] (imputed) 0 N-acetylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0800077 GCST90265574 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylhistamine levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7724339] (imputed) 0 N-acetylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0800077 GCST90265575 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylhistidine levels in chronic kidney disease 4,846 European ancestry individuals NA Illumina [7724284] (imputed) 2 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90265576 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylhistidine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723637] (imputed) 1 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90265577 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylhomocitrulline levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723649] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265578 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylisoleucine levels in chronic kidney disease 4,739 European ancestry individuals NA Illumina [7724427] (imputed) 0 N-acetylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800021 GCST90265579 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylisoleucine levels in chronic kidney disease 4,882 European ancestry individuals NA Illumina [7724470] (imputed) 0 N-acetylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800021 GCST90265580 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylkynurenine (2) levels in chronic kidney disease 4,239 European ancestry individuals NA Illumina [7723259] (imputed) 4 N-acetylkynurenine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800083 GCST90265581 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylkynurenine (2) levels in chronic kidney disease 4,376 European ancestry individuals NA Illumina [7723542] (imputed) 2 N-acetylkynurenine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800083 GCST90265582 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylleucine levels in chronic kidney disease 4,859 European ancestry individuals NA Illumina [7723322] (imputed) 1 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90265583 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylleucine levels in chronic kidney disease 4,844 European ancestry individuals NA Illumina [7724239] (imputed) 1 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90265584 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylmethionine levels in chronic kidney disease 4,937 European ancestry individuals NA Illumina [7724522] (imputed) 1 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90265585 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylmethionine sulfoxide levels in chronic kidney disease 2,166 European ancestry individuals NA Illumina [7722047] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265586 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylmethionine sulfoxide levels in chronic kidney disease 4,791 European ancestry individuals NA Illumina [7724365] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265587 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylmethionine levels in chronic kidney disease 4,620 European ancestry individuals NA Illumina [7725212] (imputed) 1 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90265588 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylneuraminate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90265589 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylneuraminate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90265590 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylphenylalanine levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724451] (imputed) 3 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90265591 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylphenylalanine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723568] (imputed) 2 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90265592 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-isoputreanine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90265543 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-L-2-aminoadipic acid levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265544 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-met-phe levels in chronic kidney disease 2,737 European ancestry individuals NA Illumina [7724321] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265545 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyl-S-allyl-L-cysteine levels in chronic kidney disease 2,085 European ancestry individuals NA Illumina [7726906] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265546 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylalanine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 1 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90265547 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylalanine levels in chronic kidney disease 4,895 European ancestry individuals NA Illumina [7724342] (imputed) 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90265548 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylalliin levels in chronic kidney disease 3,699 European ancestry individuals NA Illumina [7724436] (imputed) 0 N-acetylalliin measurement http://www.ebi.ac.uk/efo/EFO_0800987 GCST90265549 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylalliin levels in chronic kidney disease 4,772 European ancestry individuals NA Illumina [7724111] (imputed) 0 N-acetylalliin measurement http://www.ebi.ac.uk/efo/EFO_0800987 GCST90265550 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylarginine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90265551 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylarginine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90265552 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylasparagine levels in chronic kidney disease 2,607 European ancestry individuals NA Illumina [7724470] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265553 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylasparagine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723622] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265554 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylaspartate (NAA) levels in chronic kidney disease 4,393 European ancestry individuals NA Illumina [7724057] (imputed) 0 N-acetylaspartate (NAA) measurement http://www.ebi.ac.uk/efo/EFO_0800012 GCST90265555 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylaspartate (NAA) levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 N-acetylaspartate (NAA) measurement http://www.ebi.ac.uk/efo/EFO_0800012 GCST90265556 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylcarnosine levels in chronic kidney disease 4,933 European ancestry individuals NA Illumina [7724149] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265557 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylcarnosine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723607] (imputed) 3 N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022101 GCST90265558 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylcitrulline levels in chronic kidney disease 3,904 European ancestry individuals NA Illumina [7722872] (imputed) 1 N-acetylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800028 GCST90265559 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylcitrulline levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 N-acetylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800028 GCST90265560 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylcysteine levels in chronic kidney disease 4,563 European ancestry individuals NA Illumina [7723085] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265561 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylglucosamine conjugate of C24H38O4 bile acid** levels in chronic kidney disease 3,793 European ancestry individuals NA Illumina [7724304] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265562 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylglucosamine conjugate of C24H40O4 bile acid** levels in chronic kidney disease 4,638 European ancestry individuals NA Illumina [7724540] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265563 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylglucosamine/N-acetylgalactosamine levels in chronic kidney disease 4,162 European ancestry individuals NA Illumina [7724391] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265564 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylglucosamine/N-acetylgalactosamine levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723670] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265565 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylglucosaminylasparagine levels in chronic kidney disease 4,604 European ancestry individuals NA Illumina [7723582] (imputed) 3 N-acetylglucosaminylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800151 GCST90265566 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylglucosaminylasparagine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 N-acetylglucosaminylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800151 GCST90265567 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methionine sulfoxide levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90265494 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methionine sulfoxide levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723540] (imputed) 1 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90265495 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methionine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90265496 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methyl glucopyranoside (alpha + beta) levels in chronic kidney disease 4,671 European ancestry individuals NA Illumina [7723721] (imputed) 1 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90265497 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methyl glucopyranoside (alpha + beta) levels in chronic kidney disease 2,726 European ancestry individuals NA Illumina [7724704] (imputed) 1 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90265498 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methyl indole-3-acetate levels in chronic kidney disease 1,529 European ancestry individuals NA Illumina [7724433] (imputed) 0 methyl indole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0801063 GCST90265499 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methyl vanillate sulfate levels in chronic kidney disease 4,166 European ancestry individuals NA Illumina [7723950] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265500 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methyl-4-hydroxybenzoate sulfate levels in chronic kidney disease 4,846 European ancestry individuals NA Illumina [7724597] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90265501 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methyl-4-hydroxybenzoate sulfate levels in chronic kidney disease 4,767 European ancestry individuals NA Illumina [7723762] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90265502 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methylmalonate (MMA) levels in chronic kidney disease 3,901 European ancestry individuals NA Illumina [7723460] (imputed) 1 methylmalonate (MMA) measurement http://www.ebi.ac.uk/efo/EFO_0800622 GCST90265503 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methylmalonate (MMA) levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723162] (imputed) 1 methylmalonate (MMA) measurement http://www.ebi.ac.uk/efo/EFO_0800622 GCST90265504 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methylnaphthyl sulfate (2)* levels in chronic kidney disease 1,727 European ancestry individuals NA Illumina [7724730] (imputed) 0 methylnaphthyl sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801021 GCST90265505 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methylsuccinate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7724072] (imputed) 1 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90265506 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methylsuccinate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723560] (imputed) 1 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90265507 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methylsuccinoylcarnitine levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723734] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265508 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methylsuccinoylcarnitine levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723391] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265509 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methylurea levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723635] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265510 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma metoprolol acid metabolite* levels in chronic kidney disease 1,420 European ancestry individuals NA Illumina [7722116] (imputed) 0 metoprolol acid metabolite measurement http://www.ebi.ac.uk/efo/EFO_0021159 GCST90265511 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine metoprolol acid metabolite* levels in chronic kidney disease 1,270 European ancestry individuals NA Illumina [7721913] (imputed) 0 metoprolol acid metabolite measurement http://www.ebi.ac.uk/efo/EFO_0021159 GCST90265512 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma metoprolol levels in chronic kidney disease 917 European ancestry individuals NA Illumina [7721360] (imputed) 1 metoprolol measurement http://www.ebi.ac.uk/efo/EFO_0801179 GCST90265513 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine metoprolol levels in chronic kidney disease 1,175 European ancestry individuals NA Illumina [7724146] (imputed) 0 metoprolol measurement http://www.ebi.ac.uk/efo/EFO_0801179 GCST90265514 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine mevalonate levels in chronic kidney disease 4,851 European ancestry individuals NA Illumina [7723835] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265515 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine mevalonolactone levels in chronic kidney disease 3,145 European ancestry individuals NA Illumina [7725866] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265516 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma mycophenolic acid levels in chronic kidney disease 308 European ancestry individuals NA Illumina [7704474] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265517 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma myo-inositol levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723738] (imputed) 0 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90265518 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylproline levels in chronic kidney disease 4,936 European ancestry individuals NA Illumina [7724667] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265593 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylproline levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724164] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265594 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylputrescine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90265595 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylputrescine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90265596 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylpyrraline levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723595] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265597 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylserine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 1 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90265598 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylserine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723558] (imputed) 0 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90265599 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyltaurine levels in chronic kidney disease 4,922 European ancestry individuals NA Illumina [7723715] (imputed) 1 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90265600 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyltaurine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90265601 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyltheanine levels in chronic kidney disease 2,988 European ancestry individuals NA Illumina [7723333] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265602 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyltheanine levels in chronic kidney disease 1,492 European ancestry individuals NA Illumina [7731751] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265603 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylthreonine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723724] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90265604 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylthreonine levels in chronic kidney disease 4,741 European ancestry individuals NA Illumina [7724525] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90265605 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyltryptophan levels in chronic kidney disease 4,946 European ancestry individuals NA Illumina [7724570] (imputed) 2 N-acetyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800018 GCST90265606 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyltryptophan levels in chronic kidney disease 4,892 European ancestry individuals NA Illumina [7724264] (imputed) 2 N-acetyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800018 GCST90265607 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetyltyrosine levels in chronic kidney disease 4,278 European ancestry individuals NA Illumina [7723239] (imputed) 2 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90265608 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetyltyrosine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723492] (imputed) 2 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90265609 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-acetylvaline levels in chronic kidney disease 4,946 European ancestry individuals NA Illumina [7724800] (imputed) 0 N-acetylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800117 GCST90265610 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-acetylvaline levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723584] (imputed) 1 N-acetylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800117 GCST90265611 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-alpha-acetylornithine levels in chronic kidney disease 4,924 European ancestry individuals NA Illumina [7724305] (imputed) 1 N-alpha-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800006 GCST90265612 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-alpha-acetylornithine levels in chronic kidney disease 4,696 European ancestry individuals NA Illumina [7724450] (imputed) 1 N-alpha-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800006 GCST90265613 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-carbamoylalanine levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723540] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265614 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-carbamoylaspartate levels in chronic kidney disease 4,715 European ancestry individuals NA Illumina [7722617] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265615 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-carbamoylsarcosine levels in chronic kidney disease 2,849 European ancestry individuals NA Illumina [7723828] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265616 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-carbamoylvaline levels in chronic kidney disease 3,213 European ancestry individuals NA Illumina [7723103] (imputed) 0 N-carbamoylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800095 GCST90265617 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-carbamoylvaline levels in chronic kidney disease 4,706 European ancestry individuals NA Illumina [7723890] (imputed) 0 N-carbamoylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800095 GCST90265618 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-delta-acetylornithine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90265619 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-delta-acetylornithine levels in chronic kidney disease 4,745 European ancestry individuals NA Illumina [7724555] (imputed) 1 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90265620 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-formylanthranilic acid levels in chronic kidney disease 4,788 European ancestry individuals NA Illumina [7723985] (imputed) 1 N-formylanthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0800069 GCST90265621 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-formylanthranilic acid levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7723858] (imputed) 1 N-formylanthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0800069 GCST90265622 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-formylmethionine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 N-formylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800128 GCST90265623 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-formylmethionine levels in chronic kidney disease 1,571 European ancestry individuals NA Illumina [7723059] (imputed) 0 N-formylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800128 GCST90265624 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-formylphenylalanine levels in chronic kidney disease 4,606 European ancestry individuals NA Illumina [7723155] (imputed) 0 N-formylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800075 GCST90265625 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-lactoyl isoleucine levels in chronic kidney disease 4,690 European ancestry individuals NA Illumina [7724074] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265626 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-lactoyl isoleucine levels in chronic kidney disease 4,899 European ancestry individuals NA Illumina [7724264] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265627 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-lactoyl leucine levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724348] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265629 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-lactoyl phenylalanine levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723549] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265630 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-lactoyl phenylalanine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723610] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265631 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-lactoyl tyrosine levels in chronic kidney disease 4,010 European ancestry individuals NA Illumina [7722219] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265632 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-lactoyl tyrosine levels in chronic kidney disease 4,839 European ancestry individuals NA Illumina [7724443] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265633 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-lactoyl valine levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724252] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265634 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-lactoyl valine levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723697] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265635 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methyl-GABA levels in chronic kidney disease 4,863 European ancestry individuals NA Illumina [7723244] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265636 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methylalanine levels in chronic kidney disease 3,909 European ancestry individuals NA Illumina [7722575] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265637 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methylglutamate levels in chronic kidney disease 4,362 European ancestry individuals NA Illumina [7723631] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265638 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methylhydantoin levels in chronic kidney disease 2,817 European ancestry individuals NA Illumina [7722086] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265639 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-methylhydroxyproline** levels in chronic kidney disease 4,741 European ancestry individuals NA Illumina [7724125] (imputed) 0 N-methylhydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800093 GCST90265640 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methylhydroxyproline** levels in chronic kidney disease 4,874 European ancestry individuals NA Illumina [7723773] (imputed) 0 N-methylhydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800093 GCST90265641 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine N-methylleucine levels in chronic kidney disease 2,044 European ancestry individuals NA Illumina [7727467] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265642 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma N-methylpipecolate levels in chronic kidney disease 4,275 European ancestry individuals NA Illumina [7723998] (imputed) 1 N-methylpipecolate measurement http://www.ebi.ac.uk/efo/EFO_0800988 GCST90265643 Genome-wide genotyping array 2022-05-10 34996992 Labadie JD 2022-01-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34996992 Genome-wide association study identifies tumor anatomical site-specific risk variants for colorectal cancer survival. Survival in colon cancer 16,964 European ancestry individuals NA Illumina [7829749] (imputed) 0 survival time, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90102456 Genome-wide genotyping array 2022-05-10 34996992 Labadie JD 2022-01-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34996992 Genome-wide association study identifies tumor anatomical site-specific risk variants for colorectal cancer survival. Survival in colon cancer (proximal) 6,214 European ancestry individuals NA Illumina [7829749] (imputed) 2 survival time, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90102457 Genome-wide genotyping array 2022-05-10 34996992 Labadie JD 2022-01-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34996992 Genome-wide association study identifies tumor anatomical site-specific risk variants for colorectal cancer survival. Survival in colon cancer (distal) 4,881 European ancestry individuals NA Illumina [7829749] (imputed) 1 survival time, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90102458 Genome-wide genotyping array 2022-05-10 34996992 Labadie JD 2022-01-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34996992 Genome-wide association study identifies tumor anatomical site-specific risk variants for colorectal cancer survival. Survival in rectal cancer 4,749 European ancestry individuals NA Illumina [7829749] (imputed) 0 survival time, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90102459 Genome-wide genotyping array 2022-12-12 36474045 Aragam KG 2022-12-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36474045 Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Coronary artery disease 181,522 European ancestry, unknown cases, 984,168 European ancestry, unknown controls NA Affymetrix, Illumina [20073070] (imputed) 366 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90132314 Genome-wide genotyping array, Targeted genotyping array [Various], Exome genotyping array [Various] 2022-12-12 36474045 Aragam KG 2022-12-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36474045 Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants. Coronary artery disease 210,842 European ancestry, East Asian ancestry, unknown cases, 1,167,328 European ancestry, East Asian ancestry, unknown controls NA Affymetrix, Illumina [20804423] (imputed) 38 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90132315 Genome-wide genotyping array, Targeted genotyping array [Various], Exome genotyping array [Various] 2023-06-19 36819030 Guo H 2023-02-03 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/36819030 A genome-wide cross-cancer meta-analysis highlights the shared genetic links of five solid cancers. Breast cancer or ovarian cancer (pleiotropy) 122,977 breast cancer cases, 25,509 ovarian cancer cases, 146,915 controls NA NR [NR] 27 breast cancer, ovarian carcinoma http://purl.obolibrary.org/obo/MONDO_0007254, http://www.ebi.ac.uk/efo/EFO_0001075 GCST90270342 Genome-wide genotyping array 2023-06-19 36819030 Guo H 2023-02-03 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/36819030 A genome-wide cross-cancer meta-analysis highlights the shared genetic links of five solid cancers. Breast cancer or lung cancer (pleiotropy) 122,977 breast cancer cases, 11,348 lung cancer cases, 121,835 controls NA NR [NR] 18 breast cancer, lung cancer http://purl.obolibrary.org/obo/MONDO_0007254, http://purl.obolibrary.org/obo/MONDO_0008903 GCST90270343 Genome-wide genotyping array 2023-06-19 36819030 Guo H 2023-02-03 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/36819030 A genome-wide cross-cancer meta-analysis highlights the shared genetic links of five solid cancers. Lung cancer or head/neck cancer (pleiotropy) 11,348 lung cancer cases, 2,497 head/neck cancer cases, 18,789 controls NA NR [NR] 3 head and neck carcinoma, lung cancer http://purl.obolibrary.org/obo/MONDO_0002038, http://purl.obolibrary.org/obo/MONDO_0008903 GCST90270344 Genome-wide genotyping array 2022-03-02 34724200 Marley AR 2021-11-01 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34724200 Citrus-Gene interaction and melanoma risk in the UK Biobank. Melanoma x citrus consumption interaction (2df) 1,563 European ancestry cases, 193,296 European ancestry controls NA Affymetrix [9981017] (imputed) 5 citrus intake measurement, melanoma http://www.ebi.ac.uk/efo/EFO_0020897, http://www.ebi.ac.uk/efo/EFO_0000756 GCST90094985 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxyphenylacetate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723571] (imputed) 2 2-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800131 GCST90264374 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxysebacate levels in chronic kidney disease 3,800 European ancestry individuals NA Illumina [7723368] (imputed) 0 2-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800571 GCST90264375 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxysebacate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723563] (imputed) 3 2-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800571 GCST90264376 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxystearate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90264377 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-isopropylmalate levels in chronic kidney disease 3,840 European ancestry individuals NA Illumina [7723569] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264378 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-isopropylmalate levels in chronic kidney disease 4,835 European ancestry individuals NA Illumina [7724375] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264379 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-keto-3-deoxy-gluconate levels in chronic kidney disease 4,725 European ancestry individuals NA Illumina [7724005] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264380 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-ketocaprylate levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7723986] (imputed) 1 2-ketocaprylate measurement http://www.ebi.ac.uk/efo/EFO_0800110 GCST90264381 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-linoleoylglycerol (18:2) levels in chronic kidney disease 4,545 European ancestry individuals NA Illumina [7723736] (imputed) 0 2-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800197 GCST90264382 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methoxyacetaminophen glucuronide* levels in chronic kidney disease 1,415 European ancestry individuals NA Illumina [7722146] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264383 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methoxyacetaminophen sulfate* levels in chronic kidney disease 1,414 European ancestry individuals NA Illumina [7721547] (imputed) 0 2-methoxyacetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021154 GCST90264384 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methoxyhydroquinone glucuronide (2) levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723739] (imputed) 0 2-methoxyhydroquinone glucuronide (2) measurement http://www.ebi.ac.uk/efo/EFO_0801057 GCST90264385 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-methoxyhydroquinone sulfate (1) levels in chronic kidney disease 4,246 European ancestry individuals NA Illumina [7724285] (imputed) 0 2-methoxyhydroquinone sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801061 GCST90264386 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methoxyhydroquinone sulfate (1) levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723621] (imputed) 0 2-methoxyhydroquinone sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801061 GCST90264387 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methoxyhydroquinone sulfate (2) levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723531] (imputed) 0 2-methoxyhydroquinone sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801062 GCST90264388 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-methoxyresorcinol sulfate levels in chronic kidney disease 3,340 European ancestry individuals NA Illumina [7723844] (imputed) 0 2-methoxyresorcinol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801000 GCST90264389 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methoxyresorcinol sulfate levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723679] (imputed) 0 2-methoxyresorcinol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801000 GCST90264390 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-methylbutyrylcarnitine (C5) levels in chronic kidney disease 4,324 European ancestry individuals NA Illumina [7723816] (imputed) 0 2-methylbutyrylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800026 GCST90264391 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methylbutyrylcarnitine (C5) levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724465] (imputed) 0 2-methylbutyrylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800026 GCST90264392 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methylbutyrylglycine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723523] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264393 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methylcitrate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723660] (imputed) 1 2-methylcitrate measurement http://www.ebi.ac.uk/efo/EFO_0801071 GCST90264394 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-methylcitrate/homocitrate levels in chronic kidney disease 3,435 European ancestry individuals NA Illumina [7722958] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264395 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methylmalonylcarnitine (C4-DC) levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 2-methylmalonylcarnitine (C4-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800250 GCST90264396 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-methylserine levels in chronic kidney disease 4,740 European ancestry individuals NA Illumina [7724645] (imputed) 0 2-methylserine measurement http://www.ebi.ac.uk/efo/EFO_0800087 GCST90264397 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-methylserine levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723649] (imputed) 2 2-methylserine measurement http://www.ebi.ac.uk/efo/EFO_0800087 GCST90264398 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma picolinate levels in chronic kidney disease 4,650 European ancestry individuals NA Illumina [7723557] (imputed) 2 picolinate measurement http://www.ebi.ac.uk/efo/EFO_0800115 GCST90265842 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine picolinate levels in chronic kidney disease 4,853 European ancestry individuals NA Illumina [7723125] (imputed) 1 picolinate measurement http://www.ebi.ac.uk/efo/EFO_0800115 GCST90265843 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma picolinoylglycine levels in chronic kidney disease 4,743 European ancestry individuals NA Illumina [7724175] (imputed) 1 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90265844 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine picolinoylglycine levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723485] (imputed) 0 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90265845 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pimelate (C7-DC) levels in chronic kidney disease 2,817 European ancestry individuals NA Illumina [7722016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265846 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pimelate (C7-DC) levels in chronic kidney disease 4,472 European ancestry individuals NA Illumina [7723534] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265847 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) levels in chronic kidney disease 4,850 European ancestry individuals NA Illumina [7723658] (imputed) 2 pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800494 GCST90265848 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723554] (imputed) 1 pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800494 GCST90265849 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pipecolate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90265850 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pipecolate levels in chronic kidney disease 4,811 European ancestry individuals NA Illumina [7724105] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90265851 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine piperidine levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7724079] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265852 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma piperine levels in chronic kidney disease 4,944 European ancestry individuals NA Illumina [7724604] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90265853 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma prednisolone levels in chronic kidney disease 319 European ancestry individuals NA Illumina [7722559] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265854 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine prednisolone levels in chronic kidney disease 458 European ancestry individuals NA Illumina [7715347] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265855 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine prednisone levels in chronic kidney disease 498 European ancestry individuals NA Illumina [7746481] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265856 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pregnanediol-3-glucuronide levels in chronic kidney disease 4,539 European ancestry individuals NA Illumina [7724388] (imputed) 1 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90265857 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pregnanediol-3-glucuronide levels in chronic kidney disease 4,894 European ancestry individuals NA Illumina [7724607] (imputed) 2 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90265858 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pregnanolone/allopregnanolone sulfate levels in chronic kidney disease 1,602 European ancestry individuals NA Illumina [7724706] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265859 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pregnenediol disulfate (C21H34O8S2)* levels in chronic kidney disease 4,867 European ancestry individuals NA Illumina [7723856] (imputed) 3 pregnenediol disulfate (C21H34O8S2) measurement http://www.ebi.ac.uk/efo/EFO_0800279 GCST90265860 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pregnenediol disulfate (C21H34O8S2)* levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724085] (imputed) 2 pregnenediol disulfate (C21H34O8S2) measurement http://www.ebi.ac.uk/efo/EFO_0800279 GCST90265861 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pregnenediol sulfate (C21H34O5S)* levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723843] (imputed) 0 pregnenediol sulfate (C21H34O5S) measurement http://www.ebi.ac.uk/efo/EFO_0800299 GCST90265862 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pregnenediol sulfate (C21H34O5S)* levels in chronic kidney disease 1,525 European ancestry individuals NA Illumina [7726616] (imputed) 0 pregnenediol sulfate (C21H34O5S) measurement http://www.ebi.ac.uk/efo/EFO_0800299 GCST90265863 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pregnenetriol disulfate* levels in chronic kidney disease 4,920 European ancestry individuals NA Illumina [7724035] (imputed) 1 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90265864 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pregnenetriol disulfate* levels in chronic kidney disease 4,898 European ancestry individuals NA Illumina [7724628] (imputed) 1 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90265865 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pregnenetriol sulfate* levels in chronic kidney disease 4,918 European ancestry individuals NA Illumina [7723700] (imputed) 1 pregnenetriol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800586 GCST90265866 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pregnenetriol sulfate* levels in chronic kidney disease 2,815 European ancestry individuals NA Illumina [7724965] (imputed) 0 pregnenetriol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800586 GCST90265867 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pregnenolone sulfate levels in chronic kidney disease 4,334 European ancestry individuals NA Illumina [7723540] (imputed) 0 pregnenolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800303 GCST90265868 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pristanate levels in chronic kidney disease 3,958 European ancestry individuals NA Illumina [7720545] (imputed) 0 pristanate measurement http://www.ebi.ac.uk/efo/EFO_0800623 GCST90265869 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pro-hydroxy-pro levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90265870 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pro-hydroxy-pro levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723558] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90265871 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma proline levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90265872 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine proline levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90265873 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma prolylglycine levels in chronic kidney disease 4,267 European ancestry individuals NA Illumina [7723310] (imputed) 1 prolylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800683 GCST90265874 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine prolylglycine levels in chronic kidney disease 4,871 European ancestry individuals NA Illumina [7723585] (imputed) 1 prolylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800683 GCST90265875 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma propionylcarnitine (C3) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 propionylcarnitine (C3) measurement http://www.ebi.ac.uk/efo/EFO_0800210 GCST90265876 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine propionylcarnitine (C3) levels in chronic kidney disease 4,802 European ancestry individuals NA Illumina [7723609] (imputed) 0 propionylcarnitine (C3) measurement http://www.ebi.ac.uk/efo/EFO_0800210 GCST90265877 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma propionylglycine levels in chronic kidney disease 3,771 European ancestry individuals NA Illumina [7723153] (imputed) 1 propionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800207 GCST90265878 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine propionylglycine levels in chronic kidney disease 1,601 European ancestry individuals NA Illumina [7722570] (imputed) 0 propionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800207 GCST90265879 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma propyl 4-hydroxybenzoate sulfate levels in chronic kidney disease 2,335 European ancestry individuals NA Illumina [7724622] (imputed) 0 propyl 4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801005 GCST90265880 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine propyl 4-hydroxybenzoate sulfate levels in chronic kidney disease 2,518 European ancestry individuals NA Illumina [7722612] (imputed) 0 propyl 4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801005 GCST90265881 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pseudouridine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723850] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90265882 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pseudouridine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90265883 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pterin levels in chronic kidney disease 4,809 European ancestry individuals NA Illumina [7723311] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265884 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pyridostigmine levels in chronic kidney disease 1,269 European ancestry individuals NA Illumina [7723495] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265885 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pyridoxal levels in chronic kidney disease 4,451 European ancestry individuals NA Illumina [7723288] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265886 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pyridoxamine levels in chronic kidney disease 2,937 European ancestry individuals NA Illumina [7724290] (imputed) 0 pyridoxamine measurement http://www.ebi.ac.uk/efo/EFO_0021837 GCST90265887 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pyridoxate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723785] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90265888 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pyridoxate levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723614] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90265889 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pyridoxine (Vitamin B6) levels in chronic kidney disease 1,836 European ancestry individuals NA Illumina [7726856] (imputed) 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST90265890 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pyroglutamine* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST90265891 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-naphthol sulfate levels in chronic kidney disease 4,553 European ancestry individuals NA Illumina [7723062] (imputed) 0 2-naphthol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801038 GCST90264399 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-naphthol sulfate levels in chronic kidney disease 1,388 European ancestry individuals NA Illumina [7731216] (imputed) 0 2-naphthol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801038 GCST90264400 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-O-methylascorbic acid levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 2-O-methylascorbic acid measurement http://www.ebi.ac.uk/efo/EFO_0800164 GCST90264401 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-O-methylascorbic acid levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 2-O-methylascorbic acid measurement http://www.ebi.ac.uk/efo/EFO_0800164 GCST90264402 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-oleoylglycerol (18:1) levels in chronic kidney disease 4,470 European ancestry individuals NA Illumina [7723637] (imputed) 0 2-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800196 GCST90264403 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-oxindole-3-acetate levels in chronic kidney disease 4,820 European ancestry individuals NA Illumina [7724094] (imputed) 0 2-oxindole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0800968 GCST90264404 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-oxo-1-pyrrolidinepropionate levels in chronic kidney disease 4,900 European ancestry individuals NA Illumina [7724333] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264405 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-oxoadipate levels in chronic kidney disease 4,857 European ancestry individuals NA Illumina [7723307] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264406 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-oxoarginine* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90264407 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-oxoarginine* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90264408 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-palmitoleoyl-GPC (16:1)* levels in chronic kidney disease 4,209 European ancestry individuals NA Illumina [7722706] (imputed) 0 2-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800240 GCST90264409 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-palmitoyl-GPC (16:0)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 2-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800241 GCST90264410 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-piperidinone levels in chronic kidney disease 4,932 European ancestry individuals NA Illumina [7724528] (imputed) 0 2-piperidinone measurement http://www.ebi.ac.uk/efo/EFO_0800980 GCST90264411 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-piperidinone levels in chronic kidney disease 4,866 European ancestry individuals NA Illumina [7723697] (imputed) 0 2-piperidinone measurement http://www.ebi.ac.uk/efo/EFO_0800980 GCST90264412 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-stearoyl-GPE (18:0)* levels in chronic kidney disease 4,938 European ancestry individuals NA Illumina [7724413] (imputed) 0 2-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800343 GCST90264413 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2,2'-Methylenebis(6-tert-butyl-p-cresol) levels in chronic kidney disease 4,939 European ancestry individuals NA Illumina [7724554] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264414 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2,3-dihydroxy-2-methylbutyrate levels in chronic kidney disease 4,797 European ancestry individuals NA Illumina [7724175] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264415 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,3-dihydroxy-2-methylbutyrate levels in chronic kidney disease 4,847 European ancestry individuals NA Illumina [7724576] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264416 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,3-dihydroxy-3-methylvalerate levels in chronic kidney disease 4,796 European ancestry individuals NA Illumina [7724773] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264417 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723816] (imputed) 2 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90264418 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA)* levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723630] (imputed) 0 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90264419 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2,3-dihydroxyisovalerate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723774] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90264420 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,3-dihydroxyisovalerate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723639] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90264421 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,3-dihydroxypyridine levels in chronic kidney disease 4,868 European ancestry individuals NA Illumina [7723725] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264422 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,3-dimethylphenol sulfate levels in chronic kidney disease 3,789 European ancestry individuals NA Illumina [7723343] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264423 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,3-dimethylsuccinate levels in chronic kidney disease 4,658 European ancestry individuals NA Illumina [7723619] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264424 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2,4-di-tert-butylphenol levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264425 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,4-dihydroxyhydrocinnamate levels in chronic kidney disease 2,038 European ancestry individuals NA Illumina [7723786] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264426 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,4,6-trihydroxybenzoate levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724181] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264427 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2,6-dihydroxybenzoic acid levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90264428 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,6-dihydroxybenzoic acid levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723531] (imputed) 0 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90264429 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,6-dimethylphenol sulfate levels in chronic kidney disease 3,946 European ancestry individuals NA Illumina [7723374] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264430 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,8-quinolinediol sulfate levels in chronic kidney disease 4,678 European ancestry individuals NA Illumina [7724458] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264431 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2,8-quinolinediol levels in chronic kidney disease 1,230 European ancestry individuals NA Illumina [7726302] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264432 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2'-deoxyadenosine levels in chronic kidney disease 1,511 European ancestry individuals NA Illumina [7719895] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264433 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2'-deoxyguanosine levels in chronic kidney disease 2,912 European ancestry individuals NA Illumina [7722338] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264434 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2'-deoxyuridine levels in chronic kidney disease 3,309 European ancestry individuals NA Illumina [7722490] (imputed) 1 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90264435 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2'-fucosyllactose levels in chronic kidney disease 716 European ancestry individuals NA Illumina [7725710] (imputed) 1 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90264436 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenethylamine levels in chronic kidney disease 2,846 European ancestry individuals NA Illumina [7723285] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265805 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenol glucuronide levels in chronic kidney disease 2,446 European ancestry individuals NA Illumina [7723347] (imputed) 0 phenol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800084 GCST90265806 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenol glucuronide levels in chronic kidney disease 4,868 European ancestry individuals NA Illumina [7723920] (imputed) 0 phenol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800084 GCST90265807 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenol sulfate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90265808 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenol sulfate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723631] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90265809 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenylacetate levels in chronic kidney disease 3,605 European ancestry individuals NA Illumina [7721770] (imputed) 0 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90265810 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetyl-beta-alanine levels in chronic kidney disease 4,456 European ancestry individuals NA Illumina [7722718] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265811 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylalanine levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723587] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265812 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylaspartate levels in chronic kidney disease 1,928 European ancestry individuals NA Illumina [7722203] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265813 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenylacetylcarnitine levels in chronic kidney disease 4,855 European ancestry individuals NA Illumina [7723256] (imputed) 0 phenylacetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800686 GCST90265814 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylcarnitine levels in chronic kidney disease 2,204 European ancestry individuals NA Illumina [7722508] (imputed) 0 phenylacetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800686 GCST90265815 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenylacetylglutamate levels in chronic kidney disease 3,464 European ancestry individuals NA Illumina [7722508] (imputed) 1 phenylacetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800687 GCST90265816 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pyroglutamine* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST90265892 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pyrraline levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723500] (imputed) 0 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90265893 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pyrraline levels in chronic kidney disease 4,895 European ancestry individuals NA Illumina [7724494] (imputed) 1 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90265894 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma pyruvate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90265895 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine pyruvate levels in chronic kidney disease 4,844 European ancestry individuals NA Illumina [7723709] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90265896 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma quinate levels in chronic kidney disease 4,947 European ancestry individuals NA Illumina [7724366] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90265897 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine quinate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90265898 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma quinolinate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90265899 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine quinolinate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723468] (imputed) 1 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90265900 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine raffinose levels in chronic kidney disease 2,726 European ancestry individuals NA Illumina [7725668] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265901 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine resveratrol disulfate (1)* levels in chronic kidney disease 1,333 European ancestry individuals NA Illumina [7726855] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265902 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma resveratrol disulfate (2)* levels in chronic kidney disease 552 European ancestry individuals NA Illumina [7709232] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265903 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine resveratrol disulfate (2)* levels in chronic kidney disease 642 European ancestry individuals NA Illumina [7735223] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265904 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine resveratrol glucuronide (2)* levels in chronic kidney disease 728 European ancestry individuals NA Illumina [7724596] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265905 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine resveratrol sulfate (1)* levels in chronic kidney disease 1,987 European ancestry individuals NA Illumina [7726280] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265906 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma retinol (Vitamin A) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90265907 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine retinol (Vitamin A) levels in chronic kidney disease 627 European ancestry individuals NA Illumina [7728796] (imputed) 0 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90265908 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ribitol levels in chronic kidney disease 4,833 European ancestry individuals NA Illumina [7724253] (imputed) 1 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90265909 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ribitol levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724067] (imputed) 1 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90265910 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine riboflavin (Vitamin B2) levels in chronic kidney disease 3,270 European ancestry individuals NA Illumina [7721616] (imputed) 0 Riboflavin measurement http://www.ebi.ac.uk/efo/EFO_0021665 GCST90265911 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ribonate levels in chronic kidney disease 4,934 European ancestry individuals NA Illumina [7724017] (imputed) 0 ribonate measurement http://www.ebi.ac.uk/efo/EFO_0800144 GCST90265912 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ribonate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 1 ribonate measurement http://www.ebi.ac.uk/efo/EFO_0800144 GCST90265913 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-(3-hydroxypropyl)mercapturic acid (HPMA) levels in chronic kidney disease 1,200 European ancestry individuals NA Illumina [7725603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265914 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S-(3-hydroxypropyl)mercapturic acid (HPMA) levels in chronic kidney disease 4,899 European ancestry individuals NA Illumina [7724388] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265915 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-1-pyrroline-5-carboxylate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723672] (imputed) 0 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90265916 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylglutamate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 1 phenylacetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800687 GCST90265817 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenylacetylglutamine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90265818 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylglutamine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90265819 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylglycine levels in chronic kidney disease 4,813 European ancestry individuals NA Illumina [7723769] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265820 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylhistidine levels in chronic kidney disease 4,893 European ancestry individuals NA Illumina [7724608] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265821 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylleucine levels in chronic kidney disease 348 European ancestry individuals NA Illumina [7757083] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265822 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylmethionine levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724491] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265823 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylphenylalanine levels in chronic kidney disease 3,380 European ancestry individuals NA Illumina [7722940] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265824 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylserine levels in chronic kidney disease 4,565 European ancestry individuals NA Illumina [7722312] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265825 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetyltaurine levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723552] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265826 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylacetylthreonine levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723637] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265827 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenylalanine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90265828 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylalanine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90265829 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylalanylglycine levels in chronic kidney disease 4,761 European ancestry individuals NA Illumina [7723502] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265830 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylalanylhydroxyproline* levels in chronic kidney disease 3,749 European ancestry individuals NA Illumina [7723635] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265831 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenyllactate (PLA) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90265832 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenyllactate (PLA) levels in chronic kidney disease 4,565 European ancestry individuals NA Illumina [7723187] (imputed) 1 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90265833 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylpropionylglycine levels in chronic kidney disease 4,695 European ancestry individuals NA Illumina [7724442] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265834 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phenylpyruvate levels in chronic kidney disease 4,782 European ancestry individuals NA Illumina [7723855] (imputed) 0 phenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800132 GCST90265835 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phenylpyruvate levels in chronic kidney disease 2,346 European ancestry individuals NA Illumina [7724578] (imputed) 0 phenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800132 GCST90265836 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phosphate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90265837 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phosphate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90265838 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phosphoethanolamine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7724090] (imputed) 0 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90265839 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine phosphoethanolamine levels in chronic kidney disease 4,789 European ancestry individuals NA Illumina [7724180] (imputed) 1 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90265840 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma phytanate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 phytanate measurement http://www.ebi.ac.uk/efo/EFO_0801065 GCST90265841 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17358 levels in chronic kidney disease 4,880 European ancestry individuals NA Illumina [7724179] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266401 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17361 levels in chronic kidney disease 1,915 European ancestry individuals NA Illumina [7723423] (imputed) 0 X-17361 measurement http://www.ebi.ac.uk/efo/EFO_0800778 GCST90266402 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17361 levels in chronic kidney disease 4,723 European ancestry individuals NA Illumina [7723776] (imputed) 0 X-17361 measurement http://www.ebi.ac.uk/efo/EFO_0800778 GCST90266403 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17365 levels in chronic kidney disease 1,751 European ancestry individuals NA Illumina [7722489] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266404 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17365 levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723511] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266405 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17367 levels in chronic kidney disease 3,853 European ancestry individuals NA Illumina [7723663] (imputed) 0 X-17367 measurement http://www.ebi.ac.uk/efo/EFO_0800779 GCST90266406 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17367 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723609] (imputed) 1 X-17367 measurement http://www.ebi.ac.uk/efo/EFO_0800779 GCST90266407 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17370 levels in chronic kidney disease 4,746 European ancestry individuals NA Illumina [7724403] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266408 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17371 levels in chronic kidney disease 2,008 European ancestry individuals NA Illumina [7720799] (imputed) 0 X-17371 measurement http://www.ebi.ac.uk/efo/EFO_0800780 GCST90266409 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17371 levels in chronic kidney disease 3,924 European ancestry individuals NA Illumina [7721910] (imputed) 0 X-17371 measurement http://www.ebi.ac.uk/efo/EFO_0800780 GCST90266410 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17398 levels in chronic kidney disease 2,088 European ancestry individuals NA Illumina [7725299] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266411 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17398 levels in chronic kidney disease 4,819 European ancestry individuals NA Illumina [7724308] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266412 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17438 levels in chronic kidney disease 4,876 European ancestry individuals NA Illumina [7723756] (imputed) 0 X-17438 measurement http://www.ebi.ac.uk/efo/EFO_0800781 GCST90266413 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17612 levels in chronic kidney disease 4,119 European ancestry individuals NA Illumina [7723335] (imputed) 0 X-17612 measurement http://www.ebi.ac.uk/efo/EFO_0800782 GCST90266414 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17612 levels in chronic kidney disease 2,497 European ancestry individuals NA Illumina [7725715] (imputed) 0 X-17612 measurement http://www.ebi.ac.uk/efo/EFO_0800782 GCST90266415 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17653 levels in chronic kidney disease 4,721 European ancestry individuals NA Illumina [7723834] (imputed) 2 X-17653 measurement http://www.ebi.ac.uk/efo/EFO_0800783 GCST90266416 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17654 levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723955] (imputed) 4 X-17654 measurement http://www.ebi.ac.uk/efo/EFO_0800784 GCST90266417 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17655 levels in chronic kidney disease 958 European ancestry individuals NA Illumina [7724231] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266418 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17655 levels in chronic kidney disease 1,847 European ancestry individuals NA Illumina [7726387] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266419 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17673 levels in chronic kidney disease 4,824 European ancestry individuals NA Illumina [7723382] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266420 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17674 levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723622] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266421 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17675 levels in chronic kidney disease 4,786 European ancestry individuals NA Illumina [7724606] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266422 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17676 levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724165] (imputed) 0 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90266423 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17676 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723614] (imputed) 0 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90266424 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17679 levels in chronic kidney disease 3,852 European ancestry individuals NA Illumina [7723488] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266425 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17323 levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724709] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266376 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17324 levels in chronic kidney disease 4,659 European ancestry individuals NA Illumina [7723683] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266377 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17325 levels in chronic kidney disease 4,549 European ancestry individuals NA Illumina [7724779] (imputed) 0 X-17325 measurement http://www.ebi.ac.uk/efo/EFO_0800771 GCST90266378 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17325 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723610] (imputed) 1 X-17325 measurement http://www.ebi.ac.uk/efo/EFO_0800771 GCST90266379 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17328 levels in chronic kidney disease 3,499 European ancestry individuals NA Illumina [7726223] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266380 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17328 levels in chronic kidney disease 4,893 European ancestry individuals NA Illumina [7724347] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266381 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17335 levels in chronic kidney disease 4,663 European ancestry individuals NA Illumina [7723288] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90266382 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17335 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90266383 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17339 levels in chronic kidney disease 4,403 European ancestry individuals NA Illumina [7723509] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266384 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17342 levels in chronic kidney disease 3,880 European ancestry individuals NA Illumina [7723851] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266385 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17343 levels in chronic kidney disease 2,608 European ancestry individuals NA Illumina [7721783] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266386 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17343 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723578] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266387 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17346 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266388 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17348 levels in chronic kidney disease 2,284 European ancestry individuals NA Illumina [7724414] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266389 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17348 levels in chronic kidney disease 4,157 European ancestry individuals NA Illumina [7721735] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266390 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17349 levels in chronic kidney disease 4,679 European ancestry individuals NA Illumina [7724091] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266391 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17351 levels in chronic kidney disease 4,533 European ancestry individuals NA Illumina [7723718] (imputed) 0 X-17351 measurement http://www.ebi.ac.uk/efo/EFO_0800774 GCST90266392 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17351 levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724579] (imputed) 0 X-17351 measurement http://www.ebi.ac.uk/efo/EFO_0800774 GCST90266393 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17353 levels in chronic kidney disease 1,074 European ancestry individuals NA Illumina [7723875] (imputed) 0 X-17353 measurement http://www.ebi.ac.uk/efo/EFO_0800775 GCST90266394 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17353 levels in chronic kidney disease 4,335 European ancestry individuals NA Illumina [7723363] (imputed) 0 X-17353 measurement http://www.ebi.ac.uk/efo/EFO_0800775 GCST90266395 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17354 levels in chronic kidney disease 2,241 European ancestry individuals NA Illumina [7722536] (imputed) 0 X-17354 measurement http://www.ebi.ac.uk/efo/EFO_0800776 GCST90266396 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17354 levels in chronic kidney disease 4,666 European ancestry individuals NA Illumina [7723680] (imputed) 0 X-17354 measurement http://www.ebi.ac.uk/efo/EFO_0800776 GCST90266397 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17355 levels in chronic kidney disease 1,296 European ancestry individuals NA Illumina [7726348] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266398 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17357 levels in chronic kidney disease 4,643 European ancestry individuals NA Illumina [7724412] (imputed) 1 X-17357 measurement http://www.ebi.ac.uk/efo/EFO_0800777 GCST90266399 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17357 levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724376] (imputed) 1 X-17357 measurement http://www.ebi.ac.uk/efo/EFO_0800777 GCST90266400 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17682 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723609] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266426 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17685 levels in chronic kidney disease 4,537 European ancestry individuals NA Illumina [7724456] (imputed) 0 X-17685 measurement http://www.ebi.ac.uk/efo/EFO_0800786 GCST90266427 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17685 levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724088] (imputed) 0 X-17685 measurement http://www.ebi.ac.uk/efo/EFO_0800786 GCST90266428 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17686 levels in chronic kidney disease 2,584 European ancestry individuals NA Illumina [7725217] (imputed) 0 X-17686 measurement http://www.ebi.ac.uk/efo/EFO_0800787 GCST90266429 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17686 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723615] (imputed) 0 X-17686 measurement http://www.ebi.ac.uk/efo/EFO_0800787 GCST90266430 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17688 levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723636] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266431 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17689 levels in chronic kidney disease 4,888 European ancestry individuals NA Illumina [7724462] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266432 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17690 levels in chronic kidney disease 4,226 European ancestry individuals NA Illumina [7722961] (imputed) 0 X-17690 measurement http://www.ebi.ac.uk/efo/EFO_0800788 GCST90266433 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17690 levels in chronic kidney disease 4,835 European ancestry individuals NA Illumina [7723972] (imputed) 0 X-17690 measurement http://www.ebi.ac.uk/efo/EFO_0800788 GCST90266434 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17692 levels in chronic kidney disease 4,889 European ancestry individuals NA Illumina [7724357] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266435 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17704 levels in chronic kidney disease 4,227 European ancestry individuals NA Illumina [7724928] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266436 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17707 levels in chronic kidney disease 2,751 European ancestry individuals NA Illumina [7723178] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266437 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17723 levels in chronic kidney disease 4,707 European ancestry individuals NA Illumina [7723771] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266438 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17733 levels in chronic kidney disease 303 European ancestry individuals NA Illumina [7699715] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266439 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17761 levels in chronic kidney disease 364 European ancestry individuals NA Illumina [7715947] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266440 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17763 levels in chronic kidney disease 2,115 European ancestry individuals NA Illumina [7724458] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266441 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17765 levels in chronic kidney disease 3,761 European ancestry individuals NA Illumina [7723061] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266442 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17825 levels in chronic kidney disease 1,393 European ancestry individuals NA Illumina [7730106] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266443 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17842 levels in chronic kidney disease 4,138 European ancestry individuals NA Illumina [7724202] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266444 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18059 levels in chronic kidney disease 4,831 European ancestry individuals NA Illumina [7724339] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266445 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18126 levels in chronic kidney disease 1,037 European ancestry individuals NA Illumina [7725318] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266446 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18240 levels in chronic kidney disease 3,157 European ancestry individuals NA Illumina [7722074] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266447 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18240 levels in chronic kidney disease 4,739 European ancestry individuals NA Illumina [7724766] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266448 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18345 levels in chronic kidney disease 2,986 European ancestry individuals NA Illumina [7723634] (imputed) 0 X-18345 measurement http://www.ebi.ac.uk/efo/EFO_0800789 GCST90266449 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18345 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723597] (imputed) 0 X-18345 measurement http://www.ebi.ac.uk/efo/EFO_0800789 GCST90266450 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18347 levels in chronic kidney disease 1,655 European ancestry individuals NA Illumina [7724940] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266451 Genome-wide genotyping array 2023-06-13 37263751 Packer RJ 2023-06-01 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/37263751 Genome-wide association study of chronic sputum production implicates loci involved in mucus production and infection. Chronic sputum production 9,714 European ancestry cases, 48,471 European ancestry controls 1,977 European ancestry cases, 17,627 European ancestry controls NR [27317434] (imputed) 6 bringing up phlegm, sputum or mucus on most days, self-reported http://www.ebi.ac.uk/efo/EFO_0009824 GCST90269902 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3beta,17beta-diol disulfate levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7723782] (imputed) 3 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90264714 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5alpha-androstan-3beta,17beta-diol disulfate levels in chronic kidney disease 3,068 European ancestry individuals NA Illumina [7722064] (imputed) 1 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90264715 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels in chronic kidney disease 3,522 European ancestry individuals NA Illumina [7724279] (imputed) 1 5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800291 GCST90264716 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels in chronic kidney disease 439 European ancestry individuals NA Illumina [7750190] (imputed) 0 5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800291 GCST90264717 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-pregnan-3beta-ol,20-one sulfate levels in chronic kidney disease 956 European ancestry individuals NA Illumina [7721540] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264718 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-pregnan-3beta,20alpha-diol disulfate levels in chronic kidney disease 4,917 European ancestry individuals NA Illumina [7724227] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264719 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5alpha-pregnan-3beta,20alpha-diol disulfate levels in chronic kidney disease 3,631 European ancestry individuals NA Illumina [7723680] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264720 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) levels in chronic kidney disease 4,492 European ancestry individuals NA Illumina [7723827] (imputed) 1 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800285 GCST90264721 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels in chronic kidney disease 3,999 European ancestry individuals NA Illumina [7724350] (imputed) 1 5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800284 GCST90264722 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-pregnan-diol disulfate levels in chronic kidney disease 1,591 European ancestry individuals NA Illumina [7726230] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90264723 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5alpha-pregnan-diol disulfate levels in chronic kidney disease 537 European ancestry individuals NA Illumina [7740380] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90264724 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 6-bromotryptophan levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723738] (imputed) 3 6-bromotryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800099 GCST90264725 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 6-hydroxyindole sulfate levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724532] (imputed) 0 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90264726 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 6-hydroxyindole sulfate levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723352] (imputed) 0 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90264727 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 6-oxopiperidine-2-carboxylate levels in chronic kidney disease 4,540 European ancestry individuals NA Illumina [7724494] (imputed) 0 6-oxopiperidine-2-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800066 GCST90264728 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 6-oxopiperidine-2-carboxylate levels in chronic kidney disease 4,209 European ancestry individuals NA Illumina [7723591] (imputed) 0 6-oxopiperidine-2-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800066 GCST90264729 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 6-sialyl-N-acetyllactosamine levels in chronic kidney disease 4,590 European ancestry individuals NA Illumina [7723993] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264730 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 6'-sialyllactose levels in chronic kidney disease 3,572 European ancestry individuals NA Illumina [7722371] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264731 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-Hoca) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264732 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 7-hydroxyindole sulfate levels in chronic kidney disease 4,557 European ancestry individuals NA Illumina [7723911] (imputed) 0 7-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800086 GCST90264733 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 7-ketodeoxycholate levels in chronic kidney disease 1,716 European ancestry individuals NA Illumina [7720897] (imputed) 0 7-ketodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800202 GCST90264734 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 7-methylguanine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90264735 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 7-methylguanine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90264736 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 7-methylurate levels in chronic kidney disease 4,799 European ancestry individuals NA Illumina [7724753] (imputed) 0 7-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0800961 GCST90264737 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 7-methylxanthine levels in chronic kidney disease 4,884 European ancestry individuals NA Illumina [7724613] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90264738 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-hydroxymethyl-2-furoic acid levels in chronic kidney disease 3,143 European ancestry individuals NA Illumina [7724773] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264689 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-hydroxymethyl-2-furoic acid levels in chronic kidney disease 4,862 European ancestry individuals NA Illumina [7723716] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264690 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-hydroxymethyl-2-furoylcarnitine* levels in chronic kidney disease 4,060 European ancestry individuals NA Illumina [7722338] (imputed) 0 5-hydroxymethyl-2-furoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801053 GCST90264691 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-hydroxymethyl-2-furoylcarnitine* levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723687] (imputed) 1 5-hydroxymethyl-2-furoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801053 GCST90264692 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-hydroxypicolinic acid levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264693 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-methylthioadenosine (MTA) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723820] (imputed) 1 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90264694 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-methylthioadenosine (MTA) levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723588] (imputed) 0 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90264695 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-methylthioribose** levels in chronic kidney disease 4,314 European ancestry individuals NA Illumina [7723959] (imputed) 0 5-methylthioribose measurement http://www.ebi.ac.uk/efo/EFO_0800040 GCST90264696 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-methylthioribose** levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 5-methylthioribose measurement http://www.ebi.ac.uk/efo/EFO_0800040 GCST90264697 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-methyluridine (ribothymidine) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723853] (imputed) 1 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90264698 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-methyluridine (ribothymidine) levels in chronic kidney disease 1,738 European ancestry individuals NA Illumina [7728878] (imputed) 0 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90264699 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-oxoproline levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90264700 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-oxoproline levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90264701 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5,6-dihydrothymine levels in chronic kidney disease 3,414 European ancestry individuals NA Illumina [7722801] (imputed) 0 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90264702 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5,6-dihydrothymine levels in chronic kidney disease 4,351 European ancestry individuals NA Illumina [7724218] (imputed) 0 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90264703 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5,6-dihydrouracil levels in chronic kidney disease 2,988 European ancestry individuals NA Illumina [7724563] (imputed) 0 5,6-dihydrouracil measurement http://www.ebi.ac.uk/efo/EFO_0800637 GCST90264704 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5,6-dihydrouridine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723704] (imputed) 0 5,6-dihydrouridine measurement http://www.ebi.ac.uk/efo/EFO_0800631 GCST90264705 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5,6-dihydrouridine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 5,6-dihydrouridine measurement http://www.ebi.ac.uk/efo/EFO_0800631 GCST90264706 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3alpha,17alpha-diol monosulfate levels in chronic kidney disease 2,851 European ancestry individuals NA Illumina [7723484] (imputed) 2 5alpha-androstan-3alpha,17alpha-diol monosulfate measurement http://www.ebi.ac.uk/efo/EFO_0800283 GCST90264707 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3alpha,17beta-diol 17-glucuronide levels in chronic kidney disease 1,878 European ancestry individuals NA Illumina [7723697] (imputed) 0 5alpha-androstan-3alpha,17beta-diol 17-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800360 GCST90264708 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3alpha,17beta-diol disulfate levels in chronic kidney disease 2,773 European ancestry individuals NA Illumina [7723002] (imputed) 1 5alpha-androstan-3alpha,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800287 GCST90264709 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels in chronic kidney disease 4,202 European ancestry individuals NA Illumina [7723359] (imputed) 2 5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800288 GCST90264710 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels in chronic kidney disease 3,417 European ancestry individuals NA Illumina [7723570] (imputed) 1 5alpha-androstan-3alpha,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800372 GCST90264711 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5alpha-androstan-3beta,17alpha-diol disulfate levels in chronic kidney disease 3,411 European ancestry individuals NA Illumina [7721622] (imputed) 0 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90264712 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5alpha-androstan-3beta,17alpha-diol disulfate levels in chronic kidney disease 1,690 European ancestry individuals NA Illumina [7726816] (imputed) 0 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90264713 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-vinylguaiacol glucuronide levels in chronic kidney disease 3,143 European ancestry individuals NA Illumina [7724045] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264664 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-vinylguaiacol glucuronide levels in chronic kidney disease 4,895 European ancestry individuals NA Illumina [7724278] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264665 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-vinylguaiacol sulfate levels in chronic kidney disease 4,718 European ancestry individuals NA Illumina [7723582] (imputed) 0 4-vinylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800998 GCST90264666 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-vinylguaiacol sulfate levels in chronic kidney disease 4,874 European ancestry individuals NA Illumina [7724141] (imputed) 0 4-vinylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800998 GCST90264667 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-vinylphenol sulfate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723867] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90264668 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-vinylphenol sulfate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723586] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90264669 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4'-hydroxypropiophenone sulfate levels in chronic kidney disease 395 European ancestry individuals NA Illumina [7749797] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264670 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-(galactosylhydroxy)-L-lysine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723606] (imputed) 0 5-(galactosylhydroxy)-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800048 GCST90264671 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-(galactosylhydroxy)-L-lysine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723579] (imputed) 1 5-(galactosylhydroxy)-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800048 GCST90264672 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-acetylamino-6-amino-3-methyluracil levels in chronic kidney disease 4,869 European ancestry individuals NA Illumina [7723881] (imputed) 1 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90264673 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-acetylamino-6-amino-3-methyluracil levels in chronic kidney disease 4,866 European ancestry individuals NA Illumina [7723714] (imputed) 1 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90264674 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-acetylamino-6-formylamino-3-methyluracil levels in chronic kidney disease 4,307 European ancestry individuals NA Illumina [7723459] (imputed) 1 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90264675 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-acetylamino-6-formylamino-3-methyluracil levels in chronic kidney disease 4,844 European ancestry individuals NA Illumina [7724830] (imputed) 1 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90264676 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-aminovalerate levels in chronic kidney disease 1,479 European ancestry individuals NA Illumina [7725167] (imputed) 1 5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800008 GCST90264677 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-bromotryptophan levels in chronic kidney disease 2,802 European ancestry individuals NA Illumina [7722534] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264678 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-dodecenoate (12:1n7) levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7723961] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264679 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-dodecenoylcarnitine (C12:1) levels in chronic kidney disease 4,833 European ancestry individuals NA Illumina [7724168] (imputed) 0 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90264680 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-dodecenoylcarnitine (C12:1) levels in chronic kidney disease 4,853 European ancestry individuals NA Illumina [7723789] (imputed) 0 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90264681 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-hydroxy-2-methylpyridine sulfate levels in chronic kidney disease 4,402 European ancestry individuals NA Illumina [7723978] (imputed) 0 5-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801051 GCST90264682 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-hydroxyhexanoate levels in chronic kidney disease 4,884 European ancestry individuals NA Illumina [7724382] (imputed) 0 5-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800206 GCST90264683 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-hydroxyindole sulfate levels in chronic kidney disease 3,789 European ancestry individuals NA Illumina [7725211] (imputed) 0 5-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800085 GCST90264684 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-hydroxyindole sulfate levels in chronic kidney disease 4,731 European ancestry individuals NA Illumina [7724488] (imputed) 1 5-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800085 GCST90264685 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-hydroxyindoleacetate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723561] (imputed) 0 5-hydroxyindoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800139 GCST90264686 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 5-hydroxylysine levels in chronic kidney disease 4,930 European ancestry individuals NA Illumina [7723941] (imputed) 1 5-hydroxylysine measurement http://www.ebi.ac.uk/efo/EFO_0800002 GCST90264687 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 5-hydroxylysine levels in chronic kidney disease 4,503 European ancestry individuals NA Illumina [7723667] (imputed) 1 5-hydroxylysine measurement http://www.ebi.ac.uk/efo/EFO_0800002 GCST90264688 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylglutarate/2-methylglutarate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264564 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylglutarylcarnitine (1) levels in chronic kidney disease 873 European ancestry individuals NA Illumina [7725682] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264565 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methylglutarylcarnitine (2) levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723737] (imputed) 2 3-methylglutarylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800074 GCST90264566 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylglutarylcarnitine (2) levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723649] (imputed) 2 3-methylglutarylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800074 GCST90264567 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methylhistidine levels in chronic kidney disease 4,953 European ancestry individuals NA Illumina [7723952] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90264568 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylhistidine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90264569 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylurate* levels in chronic kidney disease 4,861 European ancestry individuals NA Illumina [7723430] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264570 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-methylxanthine levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724860] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90264571 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-methylxanthine levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724498] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90264572 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-phenylpropionate (hydrocinnamate) levels in chronic kidney disease 4,214 European ancestry individuals NA Illumina [7723131] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264573 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-phosphoglycerate levels in chronic kidney disease 3,988 European ancestry individuals NA Illumina [7724301] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90264574 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-phosphoglycerate levels in chronic kidney disease 4,070 European ancestry individuals NA Illumina [7724354] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90264575 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-S-cysteinyl-2-methylpropanoate* levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723590] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264576 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-ureidoisobutyrate levels in chronic kidney disease 4,188 European ancestry individuals NA Illumina [7724435] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264577 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3-ureidopropionate levels in chronic kidney disease 4,921 European ancestry individuals NA Illumina [7724206] (imputed) 0 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90264578 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3-ureidopropionate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90264579 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3,4-dihydroxybutyrate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723663] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264580 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3,4-dihydroxyphenylacetate sulfate levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723418] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264581 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3,4-dihydroxyphenylacetate levels in chronic kidney disease 4,845 European ancestry individuals NA Illumina [7724483] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264582 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3,5-dichloro-2,6-dihydroxybenzoic acid levels in chronic kidney disease 4,545 European ancestry individuals NA Illumina [7722937] (imputed) 1 3,5-dichloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801054 GCST90264583 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3,5-dihydroxybenzoic acid levels in chronic kidney disease 4,743 European ancestry individuals NA Illumina [7724356] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264584 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3,7-dimethylurate levels in chronic kidney disease 3,267 European ancestry individuals NA Illumina [7721842] (imputed) 0 3,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800949 GCST90264585 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3,7-dimethylurate levels in chronic kidney disease 4,894 European ancestry individuals NA Illumina [7724565] (imputed) 1 3,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800949 GCST90264586 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3'-a-sialyl-N-acetyllactosamine levels in chronic kidney disease 4,493 European ancestry individuals NA Illumina [7724277] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264587 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3'-sialyllactose levels in chronic kidney disease 4,892 European ancestry individuals NA Illumina [7724502] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264588 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 3alpha,21-dihydroxy-5beta-pregnane-11,20-dione 21-glucuronide levels in chronic kidney disease 4,774 European ancestry individuals NA Illumina [7723779] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264589 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3beta-hydroxy-5-cholestenoate levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723513] (imputed) 1 3beta-hydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800379 GCST90264590 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 3beta,7alpha-dihydroxy-5-cholestenoate levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724443] (imputed) 0 3beta,7alpha-dihydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800251 GCST90264591 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-acetamidobenzoate levels in chronic kidney disease 669 European ancestry individuals NA Illumina [7724830] (imputed) 0 4-acetamidobenzoate measurement http://www.ebi.ac.uk/efo/EFO_0801014 GCST90264592 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetamidobenzoate levels in chronic kidney disease 1,313 European ancestry individuals NA Illumina [7723412] (imputed) 0 4-acetamidobenzoate measurement http://www.ebi.ac.uk/efo/EFO_0801014 GCST90264593 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-acetamidobutanoate levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724140] (imputed) 1 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90264594 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetamidobutanoate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723489] (imputed) 1 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90264595 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-acetamidophenol levels in chronic kidney disease 452 European ancestry individuals NA Illumina [7713096] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264596 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetamidophenol levels in chronic kidney disease 1,620 European ancestry individuals NA Illumina [7724626] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264597 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetamidophenylglucuronide levels in chronic kidney disease 2,317 European ancestry individuals NA Illumina [7722596] (imputed) 0 4-acetamidophenylglucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800940 GCST90264598 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-acetaminophen sulfate levels in chronic kidney disease 1,025 European ancestry individuals NA Illumina [7724136] (imputed) 0 4-acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021156 GCST90264599 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetaminophen sulfate levels in chronic kidney disease 2,827 European ancestry individuals NA Illumina [7723965] (imputed) 0 4-acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021156 GCST90264600 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-acetylcatechol sulfate (1) levels in chronic kidney disease 4,490 European ancestry individuals NA Illumina [7725281] (imputed) 0 4-acetylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801049 GCST90264601 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetylcatechol sulfate (1) levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723608] (imputed) 0 4-acetylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801049 GCST90264602 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-acetylcatechol sulfate (2) levels in chronic kidney disease 3,212 European ancestry individuals NA Illumina [7724031] (imputed) 0 4-acetylcatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801050 GCST90264603 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetylcatechol sulfate (2) levels in chronic kidney disease 4,766 European ancestry individuals NA Illumina [7723418] (imputed) 0 4-acetylcatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801050 GCST90264604 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-acetylphenol sulfate levels in chronic kidney disease 4,459 European ancestry individuals NA Illumina [7723063] (imputed) 0 4-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800942 GCST90264605 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-acetylphenol sulfate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723575] (imputed) 0 4-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800942 GCST90264606 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-allylcatechol sulfate levels in chronic kidney disease 4,918 European ancestry individuals NA Illumina [7723666] (imputed) 0 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90264607 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-allylcatechol sulfate levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7724019] (imputed) 0 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90264608 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-allylphenol sulfate levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723882] (imputed) 0 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90264609 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-allylphenol sulfate levels in chronic kidney disease 4,816 European ancestry individuals NA Illumina [7724094] (imputed) 0 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90264610 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-chlorobenzoic acid levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 4-chlorobenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801059 GCST90264611 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-cholesten-3-one levels in chronic kidney disease 2,570 European ancestry individuals NA Illumina [7721995] (imputed) 0 4-cholesten-3-one measurement http://www.ebi.ac.uk/efo/EFO_0800310 GCST90264612 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-ethyl-2-methoxyphenol sulfate levels in chronic kidney disease 3,031 European ancestry individuals NA Illumina [7723503] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264613 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxyphenylacetoylcarnitine levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723559] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264639 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxyphenylacetylglutamine levels in chronic kidney disease 4,222 European ancestry individuals NA Illumina [7723816] (imputed) 0 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90264640 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxyphenylacetylglutamine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723508] (imputed) 1 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90264641 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxyphenylacetylglycine levels in chronic kidney disease 3,275 European ancestry individuals NA Illumina [7724261] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264642 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxyphenylpyruvate levels in chronic kidney disease 3,619 European ancestry individuals NA Illumina [7722105] (imputed) 0 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90264643 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxyphenylpyruvate levels in chronic kidney disease 4,809 European ancestry individuals NA Illumina [7723439] (imputed) 2 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90264644 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-imidazoleacetate levels in chronic kidney disease 2,782 European ancestry individuals NA Illumina [7723620] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264645 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-imidazoleacetate levels in chronic kidney disease 4,432 European ancestry individuals NA Illumina [7724223] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264646 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-methoxyphenol sulfate levels in chronic kidney disease 4,178 European ancestry individuals NA Illumina [7724336] (imputed) 0 4-methoxyphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800080 GCST90264647 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-methoxyphenol sulfate levels in chronic kidney disease 2,418 European ancestry individuals NA Illumina [7722131] (imputed) 0 4-methoxyphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800080 GCST90264648 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-methyl-2-oxopentanoate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90264649 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-methyl-2-oxopentanoate levels in chronic kidney disease 4,080 European ancestry individuals NA Illumina [7723842] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90264650 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-methylbenzenesulfonate levels in chronic kidney disease 3,221 European ancestry individuals NA Illumina [7723444] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264651 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-methylcatechol sulfate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723826] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90264652 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-methylcatechol sulfate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90264653 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-methylguaiacol sulfate levels in chronic kidney disease 4,515 European ancestry individuals NA Illumina [7721949] (imputed) 0 4-methylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800996 GCST90264654 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-methylguaiacol sulfate levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7723878] (imputed) 0 4-methylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800996 GCST90264655 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-methylhexanoylglutamine levels in chronic kidney disease 2,797 European ancestry individuals NA Illumina [7725384] (imputed) 0 4-methylhexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800576 GCST90264656 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-methylhexanoylglutamine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 4-methylhexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800576 GCST90264657 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-methylhexanoylglycine levels in chronic kidney disease 4,717 European ancestry individuals NA Illumina [7724251] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264658 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-octenedioate levels in chronic kidney disease 4,847 European ancestry individuals NA Illumina [7724736] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264659 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-quinolinecarboxylic acid levels in chronic kidney disease 4,786 European ancestry individuals NA Illumina [7725282] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264660 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-ureidobutyrate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723484] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264661 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-vinylcatechol sulfate levels in chronic kidney disease 4,846 European ancestry individuals NA Illumina [7724378] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264662 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-vinylcatechol sulfate levels in chronic kidney disease 4,871 European ancestry individuals NA Illumina [7723549] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264663 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-ethyl-2-methoxyphenol sulfate levels in chronic kidney disease 4,785 European ancestry individuals NA Illumina [7723916] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264614 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-ethylcatechol sulfate levels in chronic kidney disease 4,915 European ancestry individuals NA Illumina [7723783] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90264615 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-ethylcatechol sulfate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723605] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90264616 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-ethylphenol glucuronide levels in chronic kidney disease 4,021 European ancestry individuals NA Illumina [7724151] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264617 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-ethylphenylsulfate levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723693] (imputed) 0 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90264618 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-ethylphenylsulfate levels in chronic kidney disease 4,818 European ancestry individuals NA Illumina [7723649] (imputed) 0 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90264619 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-guanidinobutanoate levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723725] (imputed) 1 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90264620 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-guanidinobutanoate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90264621 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxy-2-oxoglutaric acid levels in chronic kidney disease 4,823 European ancestry individuals NA Illumina [7724026] (imputed) 0 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90264622 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxybenzoate levels in chronic kidney disease 4,672 European ancestry individuals NA Illumina [7723919] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264623 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxycatechol sulfate levels in chronic kidney disease 4,892 European ancestry individuals NA Illumina [7724174] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264624 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxychlorothalonil levels in chronic kidney disease 4,276 European ancestry individuals NA Illumina [7723252] (imputed) 1 4-hydroxychlorothalonil measurement http://www.ebi.ac.uk/efo/EFO_0800992 GCST90264625 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxycinnamate sulfate levels in chronic kidney disease 4,787 European ancestry individuals NA Illumina [7724591] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264626 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxycinnamate levels in chronic kidney disease 1,759 European ancestry individuals NA Illumina [7723863] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264627 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxycoumarin levels in chronic kidney disease 3,866 European ancestry individuals NA Illumina [7721511] (imputed) 0 4-hydroxycoumarin measurement http://www.ebi.ac.uk/efo/EFO_0800959 GCST90264628 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxycoumarin levels in chronic kidney disease 381 European ancestry individuals NA Illumina [7736281] (imputed) 0 4-hydroxycoumarin measurement http://www.ebi.ac.uk/efo/EFO_0800959 GCST90264629 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxyglutamate levels in chronic kidney disease 4,618 European ancestry individuals NA Illumina [7723623] (imputed) 1 4-hydroxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800052 GCST90264630 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxyglutamate levels in chronic kidney disease 3,802 European ancestry individuals NA Illumina [7723112] (imputed) 0 4-hydroxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800052 GCST90264631 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxyhippurate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723846] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90264632 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxyhippurate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723631] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90264633 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxymandelate levels in chronic kidney disease 4,861 European ancestry individuals NA Illumina [7723470] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264634 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxynonenal levels in chronic kidney disease 3,947 European ancestry individuals NA Illumina [7723932] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264635 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxyphenylacetate levels in chronic kidney disease 3,138 European ancestry individuals NA Illumina [7723779] (imputed) 0 4-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800124 GCST90264636 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 4-hydroxyphenylacetate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723578] (imputed) 0 4-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800124 GCST90264637 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 4-hydroxyphenylacetoylcarnitine levels in chronic kidney disease 4,824 European ancestry individuals NA Illumina [7723275] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264638 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine allantoic acid levels in chronic kidney disease 4,794 European ancestry individuals NA Illumina [7723680] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264764 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma allantoin levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90264765 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine allantoin levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90264766 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma alliin levels in chronic kidney disease 2,923 European ancestry individuals NA Illumina [7724011] (imputed) 1 alliin measurement http://www.ebi.ac.uk/efo/EFO_0800970 GCST90264767 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine alliin levels in chronic kidney disease 2,701 European ancestry individuals NA Illumina [7721884] (imputed) 0 alliin measurement http://www.ebi.ac.uk/efo/EFO_0800970 GCST90264768 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine allo-isoleucine levels in chronic kidney disease 1,222 European ancestry individuals NA Illumina [7722226] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264769 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma allo-threonine levels in chronic kidney disease 2,327 European ancestry individuals NA Illumina [7723841] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264770 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine allo-threonine levels in chronic kidney disease 4,698 European ancestry individuals NA Illumina [7724845] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264771 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma allopurinol levels in chronic kidney disease 807 European ancestry individuals NA Illumina [7716402] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264772 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine allopurinol riboside levels in chronic kidney disease 1,587 European ancestry individuals NA Illumina [7722572] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264773 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine allopurinol levels in chronic kidney disease 1,329 European ancestry individuals NA Illumina [7725326] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264774 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C14H22O4 (3)* levels in chronic kidney disease 3,996 European ancestry individuals NA Illumina [7724079] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265213 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C14H26O4 (1)* levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723315] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265214 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C14H26O4 (2)* levels in chronic kidney disease 4,873 European ancestry individuals NA Illumina [7723737] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265215 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C16H30O4 (1)* levels in chronic kidney disease 4,705 European ancestry individuals NA Illumina [7723762] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265216 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C19H28O4 (1)* levels in chronic kidney disease 4,125 European ancestry individuals NA Illumina [7723913] (imputed) 0 glucuronide of C19H28O4 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800648 GCST90265217 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C19H28O4 (2)* levels in chronic kidney disease 4,108 European ancestry individuals NA Illumina [7723737] (imputed) 0 glucuronide of C19H28O4 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800649 GCST90265218 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H14O2 (1)* levels in chronic kidney disease 2,779 European ancestry individuals NA Illumina [7723951] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265219 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H14O2 (3)* levels in chronic kidney disease 4,748 European ancestry individuals NA Illumina [7724650] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265220 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H14O2 (4)* levels in chronic kidney disease 4,587 European ancestry individuals NA Illumina [7724072] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265221 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H14O2 (5)* levels in chronic kidney disease 3,026 European ancestry individuals NA Illumina [7723602] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265222 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H14O2 (6)* levels in chronic kidney disease 4,528 European ancestry individuals NA Illumina [7723583] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265223 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H16O2 (1) levels in chronic kidney disease 3,640 European ancestry individuals NA Illumina [7724730] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265224 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H16O2 (2)* levels in chronic kidney disease 4,790 European ancestry individuals NA Illumina [7724588] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265225 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C8H18O2 (2)* levels in chronic kidney disease 1,968 European ancestry individuals NA Illumina [7722418] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265226 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13846 levels in chronic kidney disease 3,537 European ancestry individuals NA Illumina [7724028] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266326 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13846 levels in chronic kidney disease 4,880 European ancestry individuals NA Illumina [7723827] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266327 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13847 levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7724189] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266328 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13866 levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723811] (imputed) 1 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90266329 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13866 levels in chronic kidney disease 4,494 European ancestry individuals NA Illumina [7725274] (imputed) 1 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90266330 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13874 levels in chronic kidney disease 4,552 European ancestry individuals NA Illumina [7723845] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266331 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-14056 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90266332 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-14056 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723473] (imputed) 1 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90266333 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-14082 levels in chronic kidney disease 3,845 European ancestry individuals NA Illumina [7723373] (imputed) 0 X-14082 measurement http://www.ebi.ac.uk/efo/EFO_0800746 GCST90266334 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-14082 levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723692] (imputed) 0 X-14082 measurement http://www.ebi.ac.uk/efo/EFO_0800746 GCST90266335 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-14837 levels in chronic kidney disease 1,201 European ancestry individuals NA Illumina [7718996] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266336 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-14904 levels in chronic kidney disease 2,130 European ancestry individuals NA Illumina [7723908] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266337 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-14939 levels in chronic kidney disease 4,945 European ancestry individuals NA Illumina [7724728] (imputed) 1 X-14939 measurement http://www.ebi.ac.uk/efo/EFO_0800747 GCST90266338 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-15136 levels in chronic kidney disease 1,427 European ancestry individuals NA Illumina [7724242] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266339 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-15220 levels in chronic kidney disease 3,539 European ancestry individuals NA Illumina [7723548] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266340 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-15245 levels in chronic kidney disease 3,132 European ancestry individuals NA Illumina [7722962] (imputed) 0 X-15245 measurement http://www.ebi.ac.uk/efo/EFO_0800748 GCST90266341 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-15461 levels in chronic kidney disease 4,831 European ancestry individuals NA Illumina [7724118] (imputed) 0 X-15461 measurement http://www.ebi.ac.uk/efo/EFO_0800749 GCST90266342 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-15461 levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723482] (imputed) 0 X-15461 measurement http://www.ebi.ac.uk/efo/EFO_0800749 GCST90266343 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-15486 levels in chronic kidney disease 4,852 European ancestry individuals NA Illumina [7723886] (imputed) 0 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90266344 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-15486 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723638] (imputed) 0 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90266345 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-15503 levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724737] (imputed) 2 X-15503 measurement http://www.ebi.ac.uk/efo/EFO_0800753 GCST90266346 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-15503 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 X-15503 measurement http://www.ebi.ac.uk/efo/EFO_0800753 GCST90266347 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-15728 levels in chronic kidney disease 4,664 European ancestry individuals NA Illumina [7722618] (imputed) 0 X-15728 measurement http://www.ebi.ac.uk/efo/EFO_0020024 GCST90266348 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-15728 levels in chronic kidney disease 4,789 European ancestry individuals NA Illumina [7724278] (imputed) 0 X-15728 measurement http://www.ebi.ac.uk/efo/EFO_0020024 GCST90266349 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-15806 levels in chronic kidney disease 2,978 European ancestry individuals NA Illumina [7724460] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266350 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13431 levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724697] (imputed) 2 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90266301 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13431 levels in chronic kidney disease 4,796 European ancestry individuals NA Illumina [7724396] (imputed) 2 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90266302 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13507 levels in chronic kidney disease 4,924 European ancestry individuals NA Illumina [7724045] (imputed) 0 X-13507 measurement http://www.ebi.ac.uk/efo/EFO_0800736 GCST90266303 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13507 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-13507 measurement http://www.ebi.ac.uk/efo/EFO_0800736 GCST90266304 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13553 levels in chronic kidney disease 4,100 European ancestry individuals NA Illumina [7722282] (imputed) 0 X-13553 measurement http://www.ebi.ac.uk/efo/EFO_0021355 GCST90266305 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13553 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723649] (imputed) 0 X-13553 measurement http://www.ebi.ac.uk/efo/EFO_0021355 GCST90266306 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13658 levels in chronic kidney disease 1,315 European ancestry individuals NA Illumina [7725717] (imputed) 0 X-13658 measurement http://www.ebi.ac.uk/efo/EFO_0021357 GCST90266307 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13684 levels in chronic kidney disease 4,920 European ancestry individuals NA Illumina [7723774] (imputed) 2 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90266308 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13684 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723545] (imputed) 3 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90266309 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13688 levels in chronic kidney disease 4,898 European ancestry individuals NA Illumina [7724336] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266310 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13693 levels in chronic kidney disease 4,769 European ancestry individuals NA Illumina [7723944] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266311 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13695 levels in chronic kidney disease 4,297 European ancestry individuals NA Illumina [7725248] (imputed) 0 X-13695 measurement http://www.ebi.ac.uk/efo/EFO_0800738 GCST90266312 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13695 levels in chronic kidney disease 4,788 European ancestry individuals NA Illumina [7724730] (imputed) 0 X-13695 measurement http://www.ebi.ac.uk/efo/EFO_0800738 GCST90266313 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13698 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723579] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266314 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13723 levels in chronic kidney disease 3,019 European ancestry individuals NA Illumina [7722122] (imputed) 0 X-13723 measurement http://www.ebi.ac.uk/efo/EFO_0800739 GCST90266315 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13723 levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723564] (imputed) 0 X-13723 measurement http://www.ebi.ac.uk/efo/EFO_0800739 GCST90266316 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13726 levels in chronic kidney disease 2,262 European ancestry individuals NA Illumina [7718912] (imputed) 0 X-13726 measurement http://www.ebi.ac.uk/efo/EFO_0800740 GCST90266317 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13726 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723627] (imputed) 0 X-13726 measurement http://www.ebi.ac.uk/efo/EFO_0800740 GCST90266318 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13728 levels in chronic kidney disease 4,789 European ancestry individuals NA Illumina [7724004] (imputed) 0 X-13728 measurement http://www.ebi.ac.uk/efo/EFO_0800741 GCST90266319 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13729 levels in chronic kidney disease 4,499 European ancestry individuals NA Illumina [7723676] (imputed) 0 X-13729 measurement http://www.ebi.ac.uk/efo/EFO_0800742 GCST90266320 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13729 levels in chronic kidney disease 4,892 European ancestry individuals NA Illumina [7724553] (imputed) 0 X-13729 measurement http://www.ebi.ac.uk/efo/EFO_0800742 GCST90266321 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13837 levels in chronic kidney disease 4,131 European ancestry individuals NA Illumina [7724345] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266322 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13838 levels in chronic kidney disease 4,220 European ancestry individuals NA Illumina [7723265] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266323 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-13844 levels in chronic kidney disease 4,549 European ancestry individuals NA Illumina [7725388] (imputed) 0 X-13844 measurement http://www.ebi.ac.uk/efo/EFO_0800744 GCST90266324 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-13844 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-13844 measurement http://www.ebi.ac.uk/efo/EFO_0800744 GCST90266325 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12713 levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723724] (imputed) 1 X-12713 measurement http://www.ebi.ac.uk/efo/EFO_0800721 GCST90266251 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12714 levels in chronic kidney disease 4,209 European ancestry individuals NA Illumina [7723518] (imputed) 0 X-12714 measurement http://www.ebi.ac.uk/efo/EFO_0800722 GCST90266252 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12714 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 X-12714 measurement http://www.ebi.ac.uk/efo/EFO_0800722 GCST90266253 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12718 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723550] (imputed) 0 X-12718 measurement http://www.ebi.ac.uk/efo/EFO_0800723 GCST90266254 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12721 levels in chronic kidney disease 406 European ancestry individuals NA Illumina [7709177] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266255 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12722 levels in chronic kidney disease 4,832 European ancestry individuals NA Illumina [7724662] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266256 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12726 levels in chronic kidney disease 3,115 European ancestry individuals NA Illumina [7722152] (imputed) 0 X-12726 measurement http://www.ebi.ac.uk/efo/EFO_0021326 GCST90266257 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12726 levels in chronic kidney disease 4,876 European ancestry individuals NA Illumina [7723731] (imputed) 0 X-12726 measurement http://www.ebi.ac.uk/efo/EFO_0021326 GCST90266258 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12729 levels in chronic kidney disease 3,926 European ancestry individuals NA Illumina [7724772] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90266259 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12729 levels in chronic kidney disease 3,135 European ancestry individuals NA Illumina [7724968] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90266260 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12730 levels in chronic kidney disease 4,335 European ancestry individuals NA Illumina [7724237] (imputed) 0 X-12730 measurement http://www.ebi.ac.uk/efo/EFO_0800724 GCST90266261 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12730 levels in chronic kidney disease 4,805 European ancestry individuals NA Illumina [7723812] (imputed) 0 X-12730 measurement http://www.ebi.ac.uk/efo/EFO_0800724 GCST90266262 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12731 levels in chronic kidney disease 3,041 European ancestry individuals NA Illumina [7723766] (imputed) 0 X-12731 measurement http://www.ebi.ac.uk/efo/EFO_0800725 GCST90266263 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12731 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723743] (imputed) 0 X-12731 measurement http://www.ebi.ac.uk/efo/EFO_0800725 GCST90266264 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12738 levels in chronic kidney disease 3,973 European ancestry individuals NA Illumina [7722865] (imputed) 0 X-12738 measurement http://www.ebi.ac.uk/efo/EFO_0800726 GCST90266265 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12738 levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723691] (imputed) 0 X-12738 measurement http://www.ebi.ac.uk/efo/EFO_0800726 GCST90266266 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12740 levels in chronic kidney disease 3,921 European ancestry individuals NA Illumina [7723986] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90266267 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12740 levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724668] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90266268 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12745 levels in chronic kidney disease 4,893 European ancestry individuals NA Illumina [7724294] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266269 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12753 levels in chronic kidney disease 1,907 European ancestry individuals NA Illumina [7720660] (imputed) 1 X-12753 measurement http://www.ebi.ac.uk/efo/EFO_0800727 GCST90266270 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12753 levels in chronic kidney disease 4,828 European ancestry individuals NA Illumina [7724158] (imputed) 1 X-12753 measurement http://www.ebi.ac.uk/efo/EFO_0800727 GCST90266271 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12798 levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723285] (imputed) 2 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90266272 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12811 levels in chronic kidney disease 3,126 European ancestry individuals NA Illumina [7721493] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266273 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12812 levels in chronic kidney disease 4,079 European ancestry individuals NA Illumina [7723255] (imputed) 0 X-12812 measurement http://www.ebi.ac.uk/efo/EFO_0800728 GCST90266274 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12812 levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723647] (imputed) 0 X-12812 measurement http://www.ebi.ac.uk/efo/EFO_0800728 GCST90266275 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-16087 levels in chronic kidney disease 4,136 European ancestry individuals NA Illumina [7723095] (imputed) 1 X-16087 measurement http://www.ebi.ac.uk/efo/EFO_0800756 GCST90266351 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-16087 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723608] (imputed) 1 X-16087 measurement http://www.ebi.ac.uk/efo/EFO_0800756 GCST90266352 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-16124 levels in chronic kidney disease 4,232 European ancestry individuals NA Illumina [7722683] (imputed) 0 X-16124 measurement http://www.ebi.ac.uk/efo/EFO_0800757 GCST90266353 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-16124 levels in chronic kidney disease 4,581 European ancestry individuals NA Illumina [7723448] (imputed) 0 X-16124 measurement http://www.ebi.ac.uk/efo/EFO_0800757 GCST90266354 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-16397 levels in chronic kidney disease 4,923 European ancestry individuals NA Illumina [7724196] (imputed) 0 X-16397 measurement http://www.ebi.ac.uk/efo/EFO_0800758 GCST90266355 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-16397 levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723522] (imputed) 0 X-16397 measurement http://www.ebi.ac.uk/efo/EFO_0800758 GCST90266356 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-16576 levels in chronic kidney disease 3,619 European ancestry individuals NA Illumina [7723242] (imputed) 1 X-16576 measurement http://www.ebi.ac.uk/efo/EFO_0800760 GCST90266357 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-16580 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90266358 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-16580 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723599] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90266359 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-16649 levels in chronic kidney disease 3,750 European ancestry individuals NA Illumina [7724185] (imputed) 0 X-16649 measurement http://www.ebi.ac.uk/efo/EFO_0800762 GCST90266360 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-16935 levels in chronic kidney disease 2,408 European ancestry individuals NA Illumina [7724823] (imputed) 0 X-16935 measurement http://www.ebi.ac.uk/efo/EFO_0800763 GCST90266361 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17009 levels in chronic kidney disease 1,479 European ancestry individuals NA Illumina [7723323] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266362 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17010 levels in chronic kidney disease 4,935 European ancestry individuals NA Illumina [7724448] (imputed) 0 X-17010 measurement http://www.ebi.ac.uk/efo/EFO_0800767 GCST90266363 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17010 levels in chronic kidney disease 4,841 European ancestry individuals NA Illumina [7725417] (imputed) 0 X-17010 measurement http://www.ebi.ac.uk/efo/EFO_0800767 GCST90266364 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17162 levels in chronic kidney disease 937 European ancestry individuals NA Illumina [7729853] (imputed) 0 X-17162 measurement http://www.ebi.ac.uk/efo/EFO_0800769 GCST90266365 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17162 levels in chronic kidney disease 2,377 European ancestry individuals NA Illumina [7723795] (imputed) 0 X-17162 measurement http://www.ebi.ac.uk/efo/EFO_0800769 GCST90266366 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17300 levels in chronic kidney disease 4,695 European ancestry individuals NA Illumina [7724726] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266367 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17301 levels in chronic kidney disease 949 European ancestry individuals NA Illumina [7736345] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266368 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17301 levels in chronic kidney disease 1,499 European ancestry individuals NA Illumina [7730159] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266369 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17303 levels in chronic kidney disease 4,028 European ancestry individuals NA Illumina [7723835] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266370 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17304 levels in chronic kidney disease 3,187 European ancestry individuals NA Illumina [7724537] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266371 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17304 levels in chronic kidney disease 4,636 European ancestry individuals NA Illumina [7725031] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266372 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17306 levels in chronic kidney disease 2,618 European ancestry individuals NA Illumina [7723626] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266373 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-17306 levels in chronic kidney disease 3,296 European ancestry individuals NA Illumina [7724031] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266374 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-17323 levels in chronic kidney disease 4,793 European ancestry individuals NA Illumina [7724401] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266375 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12813 levels in chronic kidney disease 3,843 European ancestry individuals NA Illumina [7724688] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266276 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12815 levels in chronic kidney disease 804 European ancestry individuals NA Illumina [7717196] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266277 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12815 levels in chronic kidney disease 3,971 European ancestry individuals NA Illumina [7723355] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266278 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12816 levels in chronic kidney disease 3,383 European ancestry individuals NA Illumina [7724321] (imputed) 0 X-12816 measurement http://www.ebi.ac.uk/efo/EFO_0021336 GCST90266279 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12816 levels in chronic kidney disease 3,498 European ancestry individuals NA Illumina [7724517] (imputed) 0 X-12816 measurement http://www.ebi.ac.uk/efo/EFO_0021336 GCST90266280 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12818 levels in chronic kidney disease 3,287 European ancestry individuals NA Illumina [7723988] (imputed) 0 X-12818 measurement http://www.ebi.ac.uk/efo/EFO_0800729 GCST90266281 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12818 levels in chronic kidney disease 4,873 European ancestry individuals NA Illumina [7724178] (imputed) 0 X-12818 measurement http://www.ebi.ac.uk/efo/EFO_0800729 GCST90266282 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12821 levels in chronic kidney disease 4,472 European ancestry individuals NA Illumina [7724071] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266283 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12822 levels in chronic kidney disease 4,605 European ancestry individuals NA Illumina [7723424] (imputed) 1 X-12822 measurement http://www.ebi.ac.uk/efo/EFO_0800730 GCST90266284 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12822 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723610] (imputed) 1 X-12822 measurement http://www.ebi.ac.uk/efo/EFO_0800730 GCST90266285 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12823 levels in chronic kidney disease 3,188 European ancestry individuals NA Illumina [7722683] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266286 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12828 levels in chronic kidney disease 2,451 European ancestry individuals NA Illumina [7723751] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266287 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12830 levels in chronic kidney disease 3,504 European ancestry individuals NA Illumina [7720567] (imputed) 0 X-12830 measurement http://www.ebi.ac.uk/efo/EFO_0021337 GCST90266288 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12830 levels in chronic kidney disease 4,672 European ancestry individuals NA Illumina [7723264] (imputed) 0 X-12830 measurement http://www.ebi.ac.uk/efo/EFO_0021337 GCST90266289 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12834 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723666] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266290 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12839 levels in chronic kidney disease 1,422 European ancestry individuals NA Illumina [7724219] (imputed) 0 X-12839 measurement http://www.ebi.ac.uk/efo/EFO_0800731 GCST90266291 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12839 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723649] (imputed) 2 X-12839 measurement http://www.ebi.ac.uk/efo/EFO_0800731 GCST90266292 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12844 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723763] (imputed) 1 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90266293 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12844 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90266294 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12847 levels in chronic kidney disease 4,728 European ancestry individuals NA Illumina [7724614] (imputed) 0 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90266295 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12847 levels in chronic kidney disease 4,760 European ancestry individuals NA Illumina [7723838] (imputed) 0 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90266296 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12849 levels in chronic kidney disease 4,504 European ancestry individuals NA Illumina [7722686] (imputed) 0 X-12849 measurement http://www.ebi.ac.uk/efo/EFO_0800732 GCST90266297 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12849 levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723462] (imputed) 0 X-12849 measurement http://www.ebi.ac.uk/efo/EFO_0800732 GCST90266298 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-12851 levels in chronic kidney disease 3,037 European ancestry individuals NA Illumina [7721822] (imputed) 0 X-12851 measurement http://www.ebi.ac.uk/efo/EFO_0021342 GCST90266299 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-12906 levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723492] (imputed) 0 X-12906 measurement http://www.ebi.ac.uk/efo/EFO_0800733 GCST90266300 Genome-wide genotyping array 2023-05-15 36585402 Shaqiri A 2022-12-31 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/36585402 Visual masking deficits in schizophrenia: a view into the genetics of the disease through an endophenotype. Visual backward masking performance (SOA25) 458 Georgian ancestry individuals NA Illumina [3500000] (imputed) 3 visual masking mesurement http://www.ebi.ac.uk/efo/EFO_0803378 GCST90255670 Genome-wide genotyping array 2023-05-15 36585402 Shaqiri A 2022-12-31 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/36585402 Visual masking deficits in schizophrenia: a view into the genetics of the disease through an endophenotype. Visual backward masking performance (SOA5) 458 Georgian ancestry individuals NA Illumina [3500000] (imputed) 1 visual masking mesurement http://www.ebi.ac.uk/efo/EFO_0803378 GCST90255671 Genome-wide genotyping array 2022-03-07 35210625 Barc J 2022-02-24 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35210625 Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Brugada syndrome 2,820 European ancestry cases, 10,001 European ancestry controls NA Affymetrix, Illumina [6990521] (imputed) 21 Brugada syndrome http://purl.obolibrary.org/obo/MONDO_0015263 GCST90086158 Genome-wide genotyping array 2023-06-16 36653889 Jin H 2023-01-19 Diabetes Metab J www.ncbi.nlm.nih.gov/pubmed/36653889 Genome-Wide Association Study on Longitudinal Change in Fasting Plasma Glucose in Korean Population. Fasting plasma glucose 1,027 East Asian ancestry cases, 9,501 East Asian ancestry controls NA Affymetrix [2713317] (imputed) 4 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90270292 Genome-wide genotyping array 2023-06-16 36653889 Jin H 2023-01-19 Diabetes Metab J www.ncbi.nlm.nih.gov/pubmed/36653889 Genome-Wide Association Study on Longitudinal Change in Fasting Plasma Glucose in Korean Population. Fasting plasma glucose change 1,027 East Asian ancestry cases, 9,501 East Asian ancestry controls NA Affymetrix [2713317] (imputed) 4 fasting blood glucose change measurement http://www.ebi.ac.uk/efo/EFO_0010120 GCST90270293 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Creatinine enzymatic in urine (UKB data field 30510) 396,837 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 creatinine clearance measurement http://www.ebi.ac.uk/efo/EFO_0007934 GCST90013987 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Potassium in urine (UKB data field 30520) 395,995 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 urinary potassium measurement http://www.ebi.ac.uk/efo/EFO_0010952 GCST90013988 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Sodium in urine (UKB data field 30530) 396,020 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST90013989 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Albumin levels (UKB data field 30600) 357,968 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90013990 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Alkaline phosphatase levels (UKB data field 30610) 389,883 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90013991 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Alanine aminotransferase levels (UKB data field 30620) 389,733 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90013992 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Apolipoprotein A levels (UKB data field 30630) 355,859 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90013993 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Apolipoprotein B levels (UKB data field 30640) 388,022 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90013994 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Peak expiratory flow (UKB data field 3064) 374,599 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90013995 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Aspartate aminotransferase levels (UKB data field 30650) 388,490 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90013996 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Direct bilirubin levels (UKB data field 30660) 332,739 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90013997 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Urea levels (UKB data field 30670) 389,608 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90013998 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Calcium levels (UKB data field 30680) 357,831 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90013999 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cholesterol levels (UKB data field 30690) 389,864 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90014000 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Creatinine levels (UKB data field 30700) 389,678 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90014001 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. C reactive protein levels (UKB data field 30710) 389,057 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90014002 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cystatin C levels (UKB data field 30720) 389,834 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90014003 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Gamma glutamyltransferase levels (UKB data field 30730) 389,672 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90014004 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Glucose levels (UKB data field 30740) 357,580 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90014005 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Glycated haemoglobin HbA1c levels (UKB data field 30750) 389,889 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90014006 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. High density lipoprotein cholesterol levels (UKB data field 30760) 357,810 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90014007 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. IGF 1 (UKB data field 30770) 387,834 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90014008 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Direct low density lipoprotein levels (UKB data field 30780) 389,189 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90014009 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Phosphate levels (UKB data field 30810) 357,302 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90014010 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Sex hormone binding globulin levels (UKB data field 30830) 354,620 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90014011 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Chest pain or discomfort (UKB data field 2335) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90013962 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Fractured bones in last 5 years (UKB data field 2463) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90013963 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Reason for glasses/contact lenses: short-sightedness (UKB data field 6147_1) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90013964 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cataract (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90013965 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. High blood pressure (UKB data field 6150) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Increased blood pressure http://purl.obolibrary.org/obo/HP_0032263 GCST90013966 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Pain type(s) experienced in last month: Headache (UKB data field 6159_1) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90013967 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Pain type(s) experienced in last month: Hip pain (UKB data field 6159_6) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90013968 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Cholesterol lowering medication use (UKB data field 6177_1) (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90013969 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Allergic rhinitis (SPA correction) 407,746 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90013970 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Any parental history of Alzheimer's disease (SPA correction) 407,089 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90013971 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Any parental history of lung cancer (SPA correction) 407,521 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0006953 GCST90013972 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Townsend deprivation index at recruitment (UKB data field 189) 407,271 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 Townsend deprivation index http://www.ebi.ac.uk/efo/EFO_0009711 GCST90013973 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Body mass index (UKB data field 21001) 407,609 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90013974 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Body fat percentage (UKB data field 23099) 401,772 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90013975 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. White blood cell leukocyte count (UKB data field 30000) 396,621 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90013976 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Red blood cell erythrocyte count (UKB data field 30010) 396,625 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90013977 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Haemoglobin concentration (UKB data field 30020) 396,624 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90013978 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Mean corpuscular volume (UKB data field 30040) 396,624 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90013979 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Platelet count (UKB data field 30080) 396,621 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90013980 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Mean platelet thrombocyte volume (UKB data field 30100) 396,616 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90013981 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Lymphocyte count (UKB data field 30120) 395,949 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90013982 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Monocyte count (UKB data field 30130) 395,949 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90013983 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Neutrophill count (UKB data field 30140) 395,949 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90013984 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Eosinophill count (UKB data field 30150) 395,949 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90013985 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Basophil count 395,949 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90013986 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Total bilirubin levels (UKB data field 30840) 388,303 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90014012 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Testosterone levels (UKB data field 30850) 353,805 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90014013 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Triglyceride levels (UKB data field 30870) 389,562 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90014014 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Urate levels (UKB data field 30880) 389,404 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90014015 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Vitamin D levels (UKB data field 30890) 373,045 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90014016 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Diastolic blood pressure automated reading (UKB data field 4079) 385,801 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90014017 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Systolic blood pressure automated reading (UKB data field 4080) 385,798 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90014018 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Hand grip strength left (UKB data field 46) 406,552 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90014019 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Waist circumference (UKB data field 48) 407,661 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90014020 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Hip circumference (UKB data field 49) 407,662 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90014021 Genome-wide genotyping array 2022-04-08 34017140 Mbatchou J 2021-05-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34017140 Computationally efficient whole-genome regression for quantitative and binary traits. Bone mineral density 365,403 British ancestry individuals NA Affymetrix [11914699] (imputed) 0 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90014022 Genome-wide genotyping array 2022-05-25 35530157 Mao C 2021-10-16 Acta Pharm Sin B www.ncbi.nlm.nih.gov/pubmed/35530157 Genome-wide analysis identify novel germline genetic variations in ADCY1 influencing platinum-based chemotherapy response in non-small cell lung cancer. Response to platinum-based chemotherapy in non-small-cell lung cancer 17 Chinese ancestry cases, 17 Chinese ancestry controls 82 Chinese ancestry cases, 180 Chinese ancestry controls Illumina [142805] 0 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST90103797 Exome-wide sequencing 2022-05-25 35530157 Mao C 2021-10-16 Acta Pharm Sin B www.ncbi.nlm.nih.gov/pubmed/35530157 Genome-wide analysis identify novel germline genetic variations in ADCY1 influencing platinum-based chemotherapy response in non-small cell lung cancer. Response to platinum-based chemotherapy in non-small-cell lung cancer 206 Chinese ancestry cases, 227 Chinese ancestry controls 145 Chinese ancestry cases, 302 Chinese ancestry controls Illumina [6411261] (imputed) 2 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST90103798 Genome-wide genotyping array 2022-06-07 35299963 Lin L 2022-03-01 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35299963 Genetic Variants Relate to Fasting Plasma Glucose, 2-Hour Postprandial Glucose, Glycosylated Hemoglobin, and BMI in Prediabetes. Fasting plasma glucose in prediabetes 451 East Asian ancestry individuals NA Affymetrix [1752717] (imputed) 2 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90104039 Genome-wide genotyping array 2022-06-07 35299963 Lin L 2022-03-01 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35299963 Genetic Variants Relate to Fasting Plasma Glucose, 2-Hour Postprandial Glucose, Glycosylated Hemoglobin, and BMI in Prediabetes. Postprandial glucose in prediabetes 451 East Asian ancestry individuals NA Affymetrix [1752717] (imputed) 3 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90104040 Genome-wide genotyping array 2022-06-07 35299963 Lin L 2022-03-01 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35299963 Genetic Variants Relate to Fasting Plasma Glucose, 2-Hour Postprandial Glucose, Glycosylated Hemoglobin, and BMI in Prediabetes. Glycated hemoglobin levels in prediabetes 451 East Asian ancestry individuals NA Affymetrix [1752717] (imputed) 4 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90104041 Genome-wide genotyping array 2022-06-07 35299963 Lin L 2022-03-01 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35299963 Genetic Variants Relate to Fasting Plasma Glucose, 2-Hour Postprandial Glucose, Glycosylated Hemoglobin, and BMI in Prediabetes. Body mass index in prediabetes 451 East Asian ancestry individuals NA Affymetrix [1752717] (imputed) 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104042 Genome-wide genotyping array 2022-02-24 34779240 Cheng B 2021-11-01 Bone Joint Res www.ncbi.nlm.nih.gov/pubmed/34779240 Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort. L1-L4 bone mineral density x gut microbiota (genus Escherichia Shigella) interaction 2,293 European ancestry individuals NA Affymetrix [509886] (imputed) 1 gut microbiome measurement, spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007874, http://www.ebi.ac.uk/efo/EFO_0007701 GCST90094981 Genome-wide genotyping array 2022-02-24 34779240 Cheng B 2021-11-01 Bone Joint Res www.ncbi.nlm.nih.gov/pubmed/34779240 Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort. Total bone mineral density x gut microbiota (genus Dialister) interaction 2,293 European ancestry individuals NA Affymetrix [509886] (imputed) 19 gut microbiome measurement, bone density http://www.ebi.ac.uk/efo/EFO_0007874, http://www.ebi.ac.uk/efo/EFO_0003923 GCST90094982 Genome-wide genotyping array 2022-02-24 34779240 Cheng B 2021-11-01 Bone Joint Res www.ncbi.nlm.nih.gov/pubmed/34779240 Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort. Femur total bone mineral density x gut microbiota (genus Lactococcus) interaction 2,293 European ancestry individuals NA Affymetrix [509886] (imputed) 76 gut microbiome measurement, bone density http://www.ebi.ac.uk/efo/EFO_0007874, http://www.ebi.ac.uk/efo/EFO_0003923 GCST90094983 Genome-wide genotyping array 2022-02-24 34779240 Cheng B 2021-11-01 Bone Joint Res www.ncbi.nlm.nih.gov/pubmed/34779240 Gut microbiota is associated with bone mineral density : an observational and genome-wide environmental interaction analysis in the UK Biobank cohort. Femur total bone mineral density x gut microbiota (genus Escherichia Shigella) interaction 2,293 European ancestry individuals NA Affymetrix [509886] (imputed) 1 gut microbiome measurement, bone density http://www.ebi.ac.uk/efo/EFO_0007874, http://www.ebi.ac.uk/efo/EFO_0003923 GCST90094984 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90264274 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-GPC (16:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 1-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800214 GCST90264275 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-GPE (16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800245 GCST90264276 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-GPG (16:0)* levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724036] (imputed) 1 1-palmitoyl-GPG (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800367 GCST90264277 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-GPI (16:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-palmitoyl-GPI (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800257 GCST90264278 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoylglycerol (16:0) levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7724093] (imputed) 0 1-palmitoylglycerol (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800194 GCST90264279 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-ribosyl-imidazoleacetate* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90264280 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-ribosyl-imidazoleacetate* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90264281 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90264282 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) levels in chronic kidney disease 785 European ancestry individuals NA Illumina [7733271] (imputed) 0 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90264283 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800403 GCST90264284 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 4 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800184 GCST90264285 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800392 GCST90264286 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6)* levels in chronic kidney disease 4,946 European ancestry individuals NA Illumina [7724749] (imputed) 1 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800411 GCST90264287 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-linoleoyl-GPC (18:0/18:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90264288 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-stearoyl-2-linoleoyl-GPC (18:0/18:2)* levels in chronic kidney disease 1,714 European ancestry individuals NA Illumina [7722575] (imputed) 0 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90264289 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-linoleoyl-GPE (18:0/18:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90264290 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 3 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800413 GCST90264291 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-oleoyl-GPC (18:0/18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-stearoyl-2-oleoyl-GPC (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800389 GCST90264292 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-oleoyl-GPE (18:0/18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-stearoyl-2-oleoyl-GPE (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800269 GCST90264293 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-oleoyl-GPI (18:0/18:1)* levels in chronic kidney disease 4,942 European ancestry individuals NA Illumina [7724489] (imputed) 3 1-stearoyl-2-oleoyl-GPI (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800469 GCST90264294 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-2-oleoyl-GPS (18:0/18:1) levels in chronic kidney disease 4,178 European ancestry individuals NA Illumina [7723646] (imputed) 0 1-stearoyl-2-oleoyl-GPS (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800187 GCST90264295 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-GPC (18:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-stearoyl-GPC (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800217 GCST90264296 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-GPE (18:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800227 GCST90264297 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-GPG (18:0) levels in chronic kidney disease 4,045 European ancestry individuals NA Illumina [7723861] (imputed) 0 1-stearoyl-GPG (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800228 GCST90264298 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-GPC (P-16:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-(1-enyl-palmitoyl)-GPC (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800323 GCST90264199 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-GPE (P-16:0)* levels in chronic kidney disease 4,946 European ancestry individuals NA Illumina [7724455] (imputed) 0 1-(1-enyl-palmitoyl)-GPE (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800334 GCST90264200 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800415 GCST90264201 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90264202 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723799] (imputed) 0 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800395 GCST90264203 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-stearoyl)-GPE (P-18:0)* levels in chronic kidney disease 4,936 European ancestry individuals NA Illumina [7724206] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264204 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-aminocyclopropanecarboxylic acid levels in chronic kidney disease 1,201 European ancestry individuals NA Illumina [7720781] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264205 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-arachidonoyl-GPC (20:4n6)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-arachidonoyl-GPC (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800234 GCST90264206 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-arachidonoyl-GPE (20:4n6)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-arachidonoyl-GPE (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800248 GCST90264207 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-arachidonoyl-GPI (20:4)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 1-arachidonoyl-GPI (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800256 GCST90264208 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-arachidonylglycerol (20:4) levels in chronic kidney disease 4,445 European ancestry individuals NA Illumina [7724375] (imputed) 1 1-arachidonylglycerol (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800224 GCST90264209 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-dihomo-linolenylglycerol (20:3) levels in chronic kidney disease 4,319 European ancestry individuals NA Illumina [7723760] (imputed) 0 1-dihomo-linolenylglycerol (20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800374 GCST90264210 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-kestose levels in chronic kidney disease 3,754 European ancestry individuals NA Illumina [7724102] (imputed) 0 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90264211 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-lignoceroyl-GPC (24:0) levels in chronic kidney disease 4,810 European ancestry individuals NA Illumina [7723657] (imputed) 0 1-lignoceroyl-GPC (24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800322 GCST90264212 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linolenoyl-GPC (18:3)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-linolenoyl-GPC (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800354 GCST90264213 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linolenoylglycerol (18:3) levels in chronic kidney disease 4,008 European ancestry individuals NA Illumina [7722547] (imputed) 0 1-linolenoylglycerol (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800225 GCST90264214 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6)* levels in chronic kidney disease 4,870 European ancestry individuals NA Illumina [7724201] (imputed) 1 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800450 GCST90264215 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3)* levels in chronic kidney disease 4,828 European ancestry individuals NA Illumina [7724422] (imputed) 1 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800483 GCST90264216 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoyl-GPA (18:2)* levels in chronic kidney disease 3,527 European ancestry individuals NA Illumina [7724597] (imputed) 0 1-linoleoyl-GPA (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800445 GCST90264217 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoyl-GPC (18:2) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800223 GCST90264218 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoyl-GPE (18:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800247 GCST90264219 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoyl-GPG (18:2)* levels in chronic kidney disease 4,568 European ancestry individuals NA Illumina [7722868] (imputed) 1 1-linoleoyl-GPG (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800472 GCST90264220 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoyl-GPI (18:2)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 1-linoleoyl-GPI (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800266 GCST90264221 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-linoleoylglycerol (18:2) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800199 GCST90264222 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methyl-4-imidazoleacetate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 1-methyl-4-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800015 GCST90264223 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoyl-2-linoleoyl-GPE (18:1/18:2)* levels in chronic kidney disease 4,921 European ancestry individuals NA Illumina [7723893] (imputed) 2 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800443 GCST90264249 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoyl-GPC (18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800218 GCST90264250 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoyl-GPE (18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800246 GCST90264251 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoyl-GPG (18:1)* levels in chronic kidney disease 4,382 European ancestry individuals NA Illumina [7723250] (imputed) 1 1-oleoyl-GPG (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800366 GCST90264252 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoyl-GPI (18:1) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723793] (imputed) 1 1-oleoyl-GPI (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800265 GCST90264253 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoylglycerol (18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723846] (imputed) 0 1-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800195 GCST90264254 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3)* levels in chronic kidney disease 4,180 European ancestry individuals NA Illumina [7723196] (imputed) 1 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800484 GCST90264255 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoleoyl-GPC (16:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800231 GCST90264256 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoleoylglycerol (16:1)* levels in chronic kidney disease 4,756 European ancestry individuals NA Illumina [7722684] (imputed) 0 1-palmitoleoylglycerol (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800398 GCST90264257 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800390 GCST90264258 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) levels in chronic kidney disease 1,384 European ancestry individuals NA Illumina [7725538] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800390 GCST90264259 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800409 GCST90264260 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4)* levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724257] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800412 GCST90264261 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6)* levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723902] (imputed) 2 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800407 GCST90264262 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800391 GCST90264263 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800410 GCST90264264 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90264265 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) levels in chronic kidney disease 2,689 European ancestry individuals NA Illumina [7724505] (imputed) 0 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90264266 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800272 GCST90264267 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels in chronic kidney disease 4,688 European ancestry individuals NA Illumina [7724527] (imputed) 2 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800609 GCST90264268 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90264269 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) levels in chronic kidney disease 2,589 European ancestry individuals NA Illumina [7724947] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90264270 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800608 GCST90264271 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-oleoyl-GPI (16:0/18:1)* levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723795] (imputed) 1 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800439 GCST90264272 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-palmitoyl-2-palmitoleoyl-GPC (16:0/16:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-palmitoyl-2-palmitoleoyl-GPC(16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800406 GCST90264273 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-stearoyl-GPI (18:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800188 GCST90264299 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,2-dilinoleoyl-GPC (18:2/18:2) levels in chronic kidney disease 4,938 European ancestry individuals NA Illumina [7724607] (imputed) 1 1,2-dilinoleoyl-GPC (18:2/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800388 GCST90264300 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,2-dilinoleoyl-GPE (18:2/18:2)* levels in chronic kidney disease 3,278 European ancestry individuals NA Illumina [7724602] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264301 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,2-dipalmitoyl-GPC (16:0/16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1,2-dipalmitoyl-GPC (16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800189 GCST90264302 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,2,3-benzenetriol sulfate (1) levels in chronic kidney disease 4,882 European ancestry individuals NA Illumina [7723899] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264303 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,2,3-benzenetriol sulfate (2) levels in chronic kidney disease 3,973 European ancestry individuals NA Illumina [7723192] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90264304 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,2,3-benzenetriol sulfate (2) levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723641] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90264305 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,2,3-butanetriol levels in chronic kidney disease 3,767 European ancestry individuals NA Illumina [7723415] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264306 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,3-dimethylurate levels in chronic kidney disease 4,421 European ancestry individuals NA Illumina [7723945] (imputed) 0 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90264307 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,3-dimethylurate levels in chronic kidney disease 4,612 European ancestry individuals NA Illumina [7723983] (imputed) 0 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90264308 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,3,7-trimethylurate levels in chronic kidney disease 4,435 European ancestry individuals NA Illumina [7725340] (imputed) 0 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90264309 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,3,7-trimethylurate levels in chronic kidney disease 4,849 European ancestry individuals NA Illumina [7725065] (imputed) 0 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90264310 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,5-anhydroglucitol (1,5-AG) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90264311 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,5-anhydroglucitol (1,5-AG) levels in chronic kidney disease 4,166 European ancestry individuals NA Illumina [7723348] (imputed) 0 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90264312 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,6-anhydroglucose levels in chronic kidney disease 4,558 European ancestry individuals NA Illumina [7722829] (imputed) 1 1,6-anhydroglucose measurement http://www.ebi.ac.uk/efo/EFO_0021028 GCST90264313 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1,7-dimethylurate levels in chronic kidney disease 4,812 European ancestry individuals NA Illumina [7723928] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90264314 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1,7-dimethylurate levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723675] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90264315 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 10-heptadecenoate (17:1n7) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 10-heptadecenoate 17:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021060 GCST90264316 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 10-nonadecenoate (19:1n9) levels in chronic kidney disease 4,948 European ancestry individuals NA Illumina [7724670] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90264317 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 10-undecenoate (11:1n1) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90264318 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 11-ketoetiocholanolone glucuronide levels in chronic kidney disease 4,778 European ancestry individuals NA Illumina [7724270] (imputed) 0 11-ketoetiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800361 GCST90264319 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 11-ketoetiocholanolone sulfate levels in chronic kidney disease 2,815 European ancestry individuals NA Illumina [7721838] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264320 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 11beta-hydroxyandrosterone glucuronide levels in chronic kidney disease 4,764 European ancestry individuals NA Illumina [7723448] (imputed) 1 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90264321 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 11beta-hydroxyandrosterone glucuronide levels in chronic kidney disease 4,893 European ancestry individuals NA Illumina [7724177] (imputed) 0 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90264322 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 11beta-hydroxyetiocholanolone glucuronide* levels in chronic kidney disease 3,773 European ancestry individuals NA Illumina [7722620] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264323 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-ethylphenylsulfate levels in chronic kidney disease 4,242 European ancestry individuals NA Illumina [7723093] (imputed) 0 2-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0800957 GCST90264349 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-furoylcarnitine levels in chronic kidney disease 4,599 European ancestry individuals NA Illumina [7724459] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264350 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-furoylcarnitine levels in chronic kidney disease 4,869 European ancestry individuals NA Illumina [7723835] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264351 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxy-3-methylvalerate levels in chronic kidney disease 4,579 European ancestry individuals NA Illumina [7724675] (imputed) 0 2-hydroxy-3-methylvalerate measurement http://www.ebi.ac.uk/efo/EFO_0800027 GCST90264352 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxy-3-methylvalerate levels in chronic kidney disease 1,562 European ancestry individuals NA Illumina [7723982] (imputed) 0 2-hydroxy-3-methylvalerate measurement http://www.ebi.ac.uk/efo/EFO_0800027 GCST90264353 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxy-4-(methylthio)butanoic acid levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723618] (imputed) 2 2-hydroxy-4-(methylthio)butanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800113 GCST90264354 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxyacetaminophen sulfate* levels in chronic kidney disease 592 European ancestry individuals NA Illumina [7739285] (imputed) 0 2-hydroxyacetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021153 GCST90264355 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxyacetaminophen sulfate* levels in chronic kidney disease 4,696 European ancestry individuals NA Illumina [7725059] (imputed) 0 2-hydroxyacetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021153 GCST90264356 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxyadipate levels in chronic kidney disease 4,847 European ancestry individuals NA Illumina [7724920] (imputed) 0 2-hydroxyadipate measurement http://www.ebi.ac.uk/efo/EFO_0800209 GCST90264357 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxyarachidate* levels in chronic kidney disease 4,598 European ancestry individuals NA Illumina [7724550] (imputed) 0 2-hydroxyarachidate measurement http://www.ebi.ac.uk/efo/EFO_0800558 GCST90264358 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxybehenate levels in chronic kidney disease 4,725 European ancestry individuals NA Illumina [7724551] (imputed) 0 2-hydroxybehenate measurement http://www.ebi.ac.uk/efo/EFO_0800522 GCST90264359 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxybutyrate/2-hydroxyisobutyrate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723785] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264360 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxybutyrate/2-hydroxyisobutyrate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723588] (imputed) 1 2-hydroxybutyrate/2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022086 GCST90264361 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxydecanoate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 2-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800347 GCST90264362 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxyglutarate levels in chronic kidney disease 4,944 European ancestry individuals NA Illumina [7724594] (imputed) 1 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90264363 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxyglutarate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90264364 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxyhippurate (salicylurate) levels in chronic kidney disease 4,806 European ancestry individuals NA Illumina [7723771] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90264365 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxyhippurate (salicylurate) levels in chronic kidney disease 4,868 European ancestry individuals NA Illumina [7723291] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90264366 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxyibuprofen levels in chronic kidney disease 587 European ancestry individuals NA Illumina [7734760] (imputed) 0 2-hydroxyibuprofen measurement http://www.ebi.ac.uk/efo/EFO_0800976 GCST90264367 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxymyristate levels in chronic kidney disease 3,105 European ancestry individuals NA Illumina [7723527] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264368 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxynervonate* levels in chronic kidney disease 4,741 European ancestry individuals NA Illumina [7724453] (imputed) 0 2-hydroxynervonate measurement http://www.ebi.ac.uk/efo/EFO_0800523 GCST90264369 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxyoctanoate levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724529] (imputed) 0 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90264370 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-hydroxyoctanoate levels in chronic kidney disease 3,373 European ancestry individuals NA Illumina [7723460] (imputed) 0 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90264371 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxypalmitate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90264372 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-hydroxyphenylacetate levels in chronic kidney disease 4,361 European ancestry individuals NA Illumina [7722752] (imputed) 2 2-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800131 GCST90264373 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 12-dehydrocholate levels in chronic kidney disease 1,354 European ancestry individuals NA Illumina [7721108] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264324 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 12,13-DiHOME levels in chronic kidney disease 4,184 European ancestry individuals NA Illumina [7724229] (imputed) 0 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90264325 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 13-HODE + 9-HODE levels in chronic kidney disease 4,941 European ancestry individuals NA Illumina [7724579] (imputed) 0 13-HODE + 9-HODE measurement http://www.ebi.ac.uk/efo/EFO_0800308 GCST90264326 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 16-hydroxypalmitate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 16-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0022077 GCST90264327 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 16a-hydroxy DHEA 3-sulfate levels in chronic kidney disease 4,880 European ancestry individuals NA Illumina [7724491] (imputed) 1 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90264328 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 16a-hydroxy DHEA 3-sulfate levels in chronic kidney disease 4,456 European ancestry individuals NA Illumina [7723922] (imputed) 1 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90264329 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 17alpha-hydroxypregnanolone glucuronide levels in chronic kidney disease 3,658 European ancestry individuals NA Illumina [7722357] (imputed) 1 17alpha-hydroxypregnanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800363 GCST90264330 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 17alpha-hydroxypregnanolone glucuronide levels in chronic kidney disease 4,375 European ancestry individuals NA Illumina [7722742] (imputed) 1 17alpha-hydroxypregnanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800363 GCST90264331 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1H-indole-7-acetic acid levels in chronic kidney disease 2,292 European ancestry individuals NA Illumina [7721930] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264332 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1H-indole-7-acetic acid levels in chronic kidney disease 2,918 European ancestry individuals NA Illumina [7721991] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264333 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-acetamidophenol sulfate levels in chronic kidney disease 4,295 European ancestry individuals NA Illumina [7724378] (imputed) 0 2-acetamidophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801001 GCST90264334 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-acetamidophenol sulfate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723752] (imputed) 1 2-acetamidophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801001 GCST90264335 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-acetolactate levels in chronic kidney disease 1,997 European ancestry individuals NA Illumina [7722856] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264336 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-aminoadipate levels in chronic kidney disease 4,472 European ancestry individuals NA Illumina [7722854] (imputed) 0 2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0800137 GCST90264337 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-aminoadipate levels in chronic kidney disease 4,725 European ancestry individuals NA Illumina [7724205] (imputed) 0 2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0800137 GCST90264338 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-aminobutyrate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90264339 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-aminobutyrate levels in chronic kidney disease 1,102 European ancestry individuals NA Illumina [7720294] (imputed) 0 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90264340 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-aminoheptanoate levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7724284] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90264341 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-aminooctanoate levels in chronic kidney disease 4,831 European ancestry individuals NA Illumina [7723713] (imputed) 1 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90264342 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-aminooctanoate levels in chronic kidney disease 1,388 European ancestry individuals NA Illumina [7727988] (imputed) 0 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90264343 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-aminophenol sulfate levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723638] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90264344 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-aminophenol sulfate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90264345 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-butenoylglycine levels in chronic kidney disease 4,704 European ancestry individuals NA Illumina [7723385] (imputed) 1 2-butenoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800556 GCST90264346 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 2-dimethylaminoethanol levels in chronic kidney disease 4,786 European ancestry individuals NA Illumina [7723719] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264347 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 2-ethylphenylsulfate levels in chronic kidney disease 2,531 European ancestry individuals NA Illumina [7721648] (imputed) 0 2-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0800957 GCST90264348 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methyl-4-imidazoleacetate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 1-methyl-4-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800015 GCST90264224 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methyl-5-imidazoleacetate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90264225 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methyl-5-imidazoleacetate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90264226 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methyl-5-imidazolelactate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90264227 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methyl-5-imidazolelactate levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724143] (imputed) 0 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90264228 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methyl-beta-carboline-3-carboxylic acid levels in chronic kidney disease 1,268 European ancestry individuals NA Illumina [7720823] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264229 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methyladenine levels in chronic kidney disease 4,892 European ancestry individuals NA Illumina [7724238] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264230 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methylguanidine levels in chronic kidney disease 4,222 European ancestry individuals NA Illumina [7722766] (imputed) 0 1-methylguanidine measurement http://www.ebi.ac.uk/efo/EFO_0800011 GCST90264231 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylguanidine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723557] (imputed) 0 1-methylguanidine measurement http://www.ebi.ac.uk/efo/EFO_0800011 GCST90264232 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylguanine levels in chronic kidney disease 2,697 European ancestry individuals NA Illumina [7724184] (imputed) 0 1-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0801093 GCST90264233 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylhistamine levels in chronic kidney disease 4,826 European ancestry individuals NA Illumina [7723814] (imputed) 1 1-methylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0801095 GCST90264234 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methylhistidine levels in chronic kidney disease 4,710 European ancestry individuals NA Illumina [7723463] (imputed) 0 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90264235 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylhistidine levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723623] (imputed) 1 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90264236 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylhypoxanthine levels in chronic kidney disease 4,899 European ancestry individuals NA Illumina [7724367] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264237 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methylnicotinamide levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723815] (imputed) 1 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90264238 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylnicotinamide levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90264239 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methylurate levels in chronic kidney disease 4,559 European ancestry individuals NA Illumina [7724105] (imputed) 1 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90264240 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylurate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90264241 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-methylxanthine levels in chronic kidney disease 4,356 European ancestry individuals NA Illumina [7723391] (imputed) 1 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90264242 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-methylxanthine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723548] (imputed) 1 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90264243 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800453 GCST90264244 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800191 GCST90264245 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-myristoylglycerol (14:0) levels in chronic kidney disease 4,715 European ancestry individuals NA Illumina [7723719] (imputed) 0 1-myristoylglycerol (14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800252 GCST90264246 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4)* levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724362] (imputed) 1 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800470 GCST90264247 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6)* levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723862] (imputed) 0 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800449 GCST90264248 Genome-wide genotyping array 2022-05-06 33755393 Min S 2021-02-22 Transplantation www.ncbi.nlm.nih.gov/pubmed/33755393 An Integrated Clinical and Genetic Prediction Model for Tacrolimus Levels in Pediatric Solid Organ Transplant Recipients. Tacrolimus trough level in transplant patients (heart, kidney, lung, and liver) 287 White ancestry children, 18 Black children, 89 Asian ancestry children, 14 Aboriginal ancestry children, 47 children 249 White ancestry children, 19 Black children, 30 Asian ancestry children, 12 Aboriginal ancestry children, 12 children Affymetrix [487795] (imputed) 2 tacrolimus measurement http://www.ebi.ac.uk/efo/EFO_0008458 GCST90102473 Genome-wide genotyping array 2023-06-21 37160831 Zhu D 2023-05-09 J Epidemiol Glob Health www.ncbi.nlm.nih.gov/pubmed/37160831 Host Genetic Factors, Comorbidities and the Risk of Severe COVID-19. Severe COVID-19 infection (severe vs non-severe) 1,287 European ancestry cases, 19,033 European ancestry controls NA Affymetrix [8378356] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90270910 Genome-wide genotyping array 2022-05-18 35028426 A Gadd D 2021-11-10 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/35028426 The genetic and epigenetic profile of serum S100β in the Lothian Birth Cohort 1936 and its relationship to Alzheimer's disease. S100 calcium-binding protein levels 769 European ancestry individuals NA Illumina [7307523] (imputed) 22 S100 calcium-binding protein B measurement http://www.ebi.ac.uk/efo/EFO_0600012 GCST90102615 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hyocholate levels in chronic kidney disease 3,021 European ancestry individuals NA Illumina [7722264] (imputed) 0 hyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800219 GCST90265373 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hypotaurine levels in chronic kidney disease 4,494 European ancestry individuals NA Illumina [7723663] (imputed) 0 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90265374 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hypotaurine levels in chronic kidney disease 1,756 European ancestry individuals NA Illumina [7722804] (imputed) 0 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90265375 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hypoxanthine levels in chronic kidney disease 4,941 European ancestry individuals NA Illumina [7724584] (imputed) 0 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90265376 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C16H18N2O5 (1)** levels in chronic kidney disease 3,565 European ancestry individuals NA Illumina [7723842] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264864 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine bilirubin degradation product, C16H18N2O5 (1)** levels in chronic kidney disease 3,021 European ancestry individuals NA Illumina [7722578] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264865 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C16H18N2O5 (2)** levels in chronic kidney disease 4,933 European ancestry individuals NA Illumina [7724405] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264866 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C16H18N2O5 (4)** levels in chronic kidney disease 4,786 European ancestry individuals NA Illumina [7724509] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264867 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C17H18N2O4 (1)** levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724498] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264868 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C17H18N2O4 (2)** levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723874] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264869 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C17H18N2O4 (3)** levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723848] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264870 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C17H20N2O5 (1)** levels in chronic kidney disease 4,764 European ancestry individuals NA Illumina [7724032] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264871 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin degradation product, C17H20N2O5 (2)** levels in chronic kidney disease 4,888 European ancestry individuals NA Illumina [7724055] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264872 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma biliverdin levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723857] (imputed) 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90264873 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine biopterin levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724516] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264874 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bradykinin levels in chronic kidney disease 352 European ancestry individuals NA Illumina [7708327] (imputed) 0 bradykinin measurement http://www.ebi.ac.uk/efo/EFO_0800665 GCST90264875 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma branched chain 14:0 dicarboxylic acid** levels in chronic kidney disease 4,793 European ancestry individuals NA Illumina [7724240] (imputed) 0 branched chain 14:0 dicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0800593 GCST90264876 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1)* levels in chronic kidney disease 4,945 European ancestry individuals NA Illumina [7724741] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) measurement http://www.ebi.ac.uk/efo/EFO_0800661 GCST90264877 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (2)* levels in chronic kidney disease 3,491 European ancestry individuals NA Illumina [7724148] (imputed) 1 branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) measurement http://www.ebi.ac.uk/efo/EFO_0800661 GCST90264878 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid* levels in chronic kidney disease 4,945 European ancestry individuals NA Illumina [7724808] (imputed) 1 branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0800662 GCST90264879 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma butyrate/isobutyrate (4:0) levels in chronic kidney disease 3,279 European ancestry individuals NA Illumina [7724090] (imputed) 0 isobutyrate (4:0) measurement, butyrate (4:0) measurement http://www.ebi.ac.uk/efo/EFO_0800605, http://www.ebi.ac.uk/efo/EFO_0801073 GCST90264880 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine butyryl-putrescine levels in chronic kidney disease 3,712 European ancestry individuals NA Illumina [7723943] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264881 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma butyrylcarnitine (C4) levels in chronic kidney disease 4,825 European ancestry individuals NA Illumina [7723900] (imputed) 2 butyrylcarnitine (C4) measurement http://www.ebi.ac.uk/efo/EFO_0800201 GCST90264882 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma C-glycosyltryptophan levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90264883 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine C-glycosyltryptophan levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90264884 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma heptadecenamide (17:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265323 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma heptanoate (7:0) levels in chronic kidney disease 3,825 European ancestry individuals NA Illumina [7723851] (imputed) 0 heptanoate 7:0 measurement http://www.ebi.ac.uk/efo/EFO_0021104 GCST90265324 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine heptanoylglutamine levels in chronic kidney disease 4,225 European ancestry individuals NA Illumina [7723272] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265325 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma heptenedioate (C7:1-DC)* levels in chronic kidney disease 4,944 European ancestry individuals NA Illumina [7724614] (imputed) 0 heptenedioate (C7:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800564 GCST90265326 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine heptenedioate (C7:1-DC)* levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 0 heptenedioate (C7:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800564 GCST90265327 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hexadecadienoate (16:2n6) levels in chronic kidney disease 4,939 European ancestry individuals NA Illumina [7724562] (imputed) 0 hexadecadienoate (16:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800491 GCST90265328 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hexadecanedioate (C16-DC) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723871] (imputed) 2 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90265329 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hexadecenedioate (C16:1-DC)* levels in chronic kidney disease 4,953 European ancestry individuals NA Illumina [7723766] (imputed) 1 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90265330 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hexanoylcarnitine (C6) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90265331 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hexanoylcarnitine (C6) levels in chronic kidney disease 3,953 European ancestry individuals NA Illumina [7722351] (imputed) 1 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90265332 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hexanoylglutamine levels in chronic kidney disease 4,808 European ancestry individuals NA Illumina [7723483] (imputed) 2 hexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800262 GCST90265333 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hexanoylglutamine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723446] (imputed) 2 hexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800262 GCST90265334 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hexanoylglycine levels in chronic kidney disease 2,699 European ancestry individuals NA Illumina [7723598] (imputed) 2 hexanoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800233 GCST90265335 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hexanoylglycine levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723616] (imputed) 2 hexanoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800233 GCST90265336 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hexanoyltaurine levels in chronic kidney disease 4,785 European ancestry individuals NA Illumina [7723605] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265337 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hippurate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90265338 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hippurate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723610] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90265339 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine histamine levels in chronic kidney disease 2,181 European ancestry individuals NA Illumina [7724087] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265340 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma histidine betaine (hercynine)* levels in chronic kidney disease 3,570 European ancestry individuals NA Illumina [7724859] (imputed) 0 histidine betaine (hercynine) measurement http://www.ebi.ac.uk/efo/EFO_0800972 GCST90265341 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine histidine betaine (hercynine)* levels in chronic kidney disease 2,737 European ancestry individuals NA Illumina [7724488] (imputed) 0 histidine betaine (hercynine) measurement http://www.ebi.ac.uk/efo/EFO_0800972 GCST90265342 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma histidine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90265343 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine histidine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723599] (imputed) 2 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90265344 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma homoarginine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265345 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homoarginine levels in chronic kidney disease 4,434 European ancestry individuals NA Illumina [7724159] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265346 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homocarnosine levels in chronic kidney disease 4,312 European ancestry individuals NA Illumina [7722939] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265347 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ceramide (d18:1/14:0, d16:1/16:0)* levels in chronic kidney disease 4,559 European ancestry individuals NA Illumina [7722463] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90264910 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cerotoylcarnitine (C26)* levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723856] (imputed) 3 cerotoylcarnitine (C26) measurement http://www.ebi.ac.uk/efo/EFO_0800542 GCST90264911 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma chenodeoxycholate levels in chronic kidney disease 4,318 European ancestry individuals NA Illumina [7722774] (imputed) 0 chenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010471 GCST90264912 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine chenodeoxycholic acid sulfate (1) levels in chronic kidney disease 1,660 European ancestry individuals NA Illumina [7719758] (imputed) 0 chenodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800596 GCST90264913 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma chiro-inositol levels in chronic kidney disease 2,644 European ancestry individuals NA Illumina [7726178] (imputed) 0 chiro-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800270 GCST90264914 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine chiro-inositol levels in chronic kidney disease 4,145 European ancestry individuals NA Illumina [7723947] (imputed) 0 chiro-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800270 GCST90264915 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine chlorogenate levels in chronic kidney disease 3,887 European ancestry individuals NA Illumina [7724423] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264916 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma chlorothiazide levels in chronic kidney disease 434 European ancestry individuals NA Illumina [7734852] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264917 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cholate levels in chronic kidney disease 4,895 European ancestry individuals NA Illumina [7724603] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90264918 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cholate levels in chronic kidney disease 3,397 European ancestry individuals NA Illumina [7722885] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90264919 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cholesterol levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90264920 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cholesterol sulfate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723867] (imputed) 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90264921 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cholic acid glucuronide levels in chronic kidney disease 2,209 European ancestry individuals NA Illumina [7721312] (imputed) 1 cholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800574 GCST90264922 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cholic acid glucuronide levels in chronic kidney disease 2,612 European ancestry individuals NA Illumina [7723363] (imputed) 1 cholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800574 GCST90264923 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma choline phosphate levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723849] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90264924 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine choline phosphate levels in chronic kidney disease 4,791 European ancestry individuals NA Illumina [7724494] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90264925 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma choline levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90264926 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine choline levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90264927 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ciliatine (2-aminoethylphosphonate) levels in chronic kidney disease 1,155 European ancestry individuals NA Illumina [7721832] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264928 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cinnamoylglycine levels in chronic kidney disease 4,305 European ancestry individuals NA Illumina [7721539] (imputed) 0 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90264929 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cinnamoylglycine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90264930 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cis-3,4-methyleneheptanoate levels in chronic kidney disease 4,200 European ancestry individuals NA Illumina [7723998] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90264931 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cis-3,4-methyleneheptanoylcarnitine levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723868] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264932 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cis-3,4-methyleneheptanoylcarnitine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723358] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264933 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cis-3,4-methyleneheptanoylglycine levels in chronic kidney disease 4,227 European ancestry individuals NA Illumina [7723719] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264934 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cis-3,4-methyleneheptanoylglycine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264935 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cis-4-decenoate (10:1n6)* levels in chronic kidney disease 4,777 European ancestry individuals NA Illumina [7723559] (imputed) 2 cis-4-decenoate (10:1n6) measurement http://www.ebi.ac.uk/efo/EFO_0800318 GCST90264936 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cis-4-decenoylcarnitine (C10:1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 cis-4-decenoylcarnitine (C10:1) measurement http://www.ebi.ac.uk/efo/EFO_0800311 GCST90264937 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cis-urocanate levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7724155] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264938 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma citraconate/glutaconate levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7724007] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264939 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine citraconate/glutaconate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723613] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264940 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine citramalate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723593] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264941 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma citrate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90264942 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine citrate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90264943 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma citrulline levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90264944 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine citrulline levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90264945 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cortisol 21-glucuronide levels in chronic kidney disease 4,486 European ancestry individuals NA Illumina [7724328] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264946 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cortisol levels in chronic kidney disease 4,800 European ancestry individuals NA Illumina [7724294] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90264947 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cortisol levels in chronic kidney disease 2,322 European ancestry individuals NA Illumina [7723412] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90264948 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cortisone 21-sulfate levels in chronic kidney disease 2,540 European ancestry individuals NA Illumina [7722826] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264949 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cortisone levels in chronic kidney disease 4,679 European ancestry individuals NA Illumina [7724168] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90264950 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cortisone levels in chronic kidney disease 4,764 European ancestry individuals NA Illumina [7723374] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90264951 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cortolone glucuronide (1) levels in chronic kidney disease 4,620 European ancestry individuals NA Illumina [7723668] (imputed) 1 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90264952 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma galactonate levels in chronic kidney disease 4,504 European ancestry individuals NA Illumina [7723968] (imputed) 0 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90265133 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine galactonate levels in chronic kidney disease 4,707 European ancestry individuals NA Illumina [7724148] (imputed) 0 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90265134 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine galactosylglycerol levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723601] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265135 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-carboxyglutamate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 gamma-carboxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800053 GCST90265136 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-CEHC glucuronide* levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723680] (imputed) 1 gamma-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800165 GCST90265137 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-CEHC levels in chronic kidney disease 4,693 European ancestry individuals NA Illumina [7724392] (imputed) 1 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90265138 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-CEHC sulfate levels in chronic kidney disease 3,241 European ancestry individuals NA Illumina [7726353] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265139 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-CEHC taurine* levels in chronic kidney disease 4,130 European ancestry individuals NA Illumina [7723742] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265140 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-CEHC levels in chronic kidney disease 1,982 European ancestry individuals NA Illumina [7725952] (imputed) 0 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90265141 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamyl-2-aminobutyrate levels in chronic kidney disease 4,726 European ancestry individuals NA Illumina [7723924] (imputed) 0 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90265142 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamyl-alpha-lysine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723733] (imputed) 0 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90265143 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamyl-alpha-lysine levels in chronic kidney disease 1,426 European ancestry individuals NA Illumina [7724832] (imputed) 0 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90265144 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamyl-epsilon-lysine levels in chronic kidney disease 4,438 European ancestry individuals NA Illumina [7724236] (imputed) 0 gamma-glutamyl-epsilon-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800667 GCST90265145 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamyl-epsilon-lysine levels in chronic kidney disease 3,405 European ancestry individuals NA Illumina [7724231] (imputed) 1 gamma-glutamyl-epsilon-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800667 GCST90265146 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylalanine levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724297] (imputed) 0 gamma-glutamylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800675 GCST90265147 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylcitrulline* levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7723890] (imputed) 0 gamma-glutamylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800690 GCST90265148 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylglutamate levels in chronic kidney disease 4,919 European ancestry individuals NA Illumina [7724073] (imputed) 0 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90265149 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylglutamine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723733] (imputed) 1 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90265150 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylglutamine levels in chronic kidney disease 864 European ancestry individuals NA Illumina [7720299] (imputed) 0 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90265151 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylglycine levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723728] (imputed) 1 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90265152 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylglycine levels in chronic kidney disease 4,163 European ancestry individuals NA Illumina [7723500] (imputed) 1 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90265153 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylhistidine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723733] (imputed) 0 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90265154 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylhistidine levels in chronic kidney disease 3,791 European ancestry individuals NA Illumina [7726028] (imputed) 1 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90265155 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylisoleucine* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90265156 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylisoleucine* levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724540] (imputed) 1 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90265157 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylleucine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723733] (imputed) 0 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90265158 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylleucine levels in chronic kidney disease 3,571 European ancestry individuals NA Illumina [7724723] (imputed) 1 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90265159 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylmethionine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723681] (imputed) 0 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90265160 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylphenylalanine levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723706] (imputed) 0 gamma-glutamylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021142 GCST90265161 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylphenylalanine levels in chronic kidney disease 4,031 European ancestry individuals NA Illumina [7724287] (imputed) 1 gamma-glutamylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021142 GCST90265162 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylthreonine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90265163 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylthreonine levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723614] (imputed) 1 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90265164 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine caffeate levels in chronic kidney disease 4,392 European ancestry individuals NA Illumina [7724774] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264885 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma caffeic acid sulfate levels in chronic kidney disease 4,766 European ancestry individuals NA Illumina [7724208] (imputed) 0 caffeic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801013 GCST90264886 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine caffeic acid sulfate levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723732] (imputed) 0 caffeic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801013 GCST90264887 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma caffeine levels in chronic kidney disease 4,803 European ancestry individuals NA Illumina [7724673] (imputed) 0 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90264888 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine caffeine levels in chronic kidney disease 4,709 European ancestry individuals NA Illumina [7724356] (imputed) 0 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90264889 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma campesterol levels in chronic kidney disease 1,551 European ancestry individuals NA Illumina [7722257] (imputed) 0 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90264890 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma candesartan levels in chronic kidney disease 670 European ancestry individuals NA Illumina [7718956] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264891 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine candesartan levels in chronic kidney disease 665 European ancestry individuals NA Illumina [7715852] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264892 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma caprate (10:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723771] (imputed) 0 caprate 10:0 measurement http://www.ebi.ac.uk/efo/EFO_0021101 GCST90264893 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma caprylate (8:0) levels in chronic kidney disease 4,380 European ancestry individuals NA Illumina [7722852] (imputed) 0 caprylate 8:0 measurement http://www.ebi.ac.uk/efo/EFO_0021103 GCST90264894 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma carboxyethyl-GABA levels in chronic kidney disease 4,953 European ancestry individuals NA Illumina [7723998] (imputed) 1 carboxyethyl-GABA measurement http://www.ebi.ac.uk/efo/EFO_0800059 GCST90264895 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine carboxyethyl-GABA levels in chronic kidney disease 4,756 European ancestry individuals NA Illumina [7723812] (imputed) 0 carboxyethyl-GABA measurement http://www.ebi.ac.uk/efo/EFO_0800059 GCST90264896 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine carboxyibuprofen levels in chronic kidney disease 828 European ancestry individuals NA Illumina [7722950] (imputed) 0 carboxyibuprofen measurement http://www.ebi.ac.uk/efo/EFO_0800977 GCST90264897 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine carnitine of C10H14O2 (5)* levels in chronic kidney disease 3,333 European ancestry individuals NA Illumina [7723677] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264898 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma carnitine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90264899 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine carnitine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90264900 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine carnosine levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723593] (imputed) 2 carnosine measurement http://www.ebi.ac.uk/efo/EFO_0010470 GCST90264901 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma carotene diol (1) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 carotene diol (1) measurement http://www.ebi.ac.uk/efo/EFO_0800170 GCST90264902 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma carotene diol (2) levels in chronic kidney disease 4,943 European ancestry individuals NA Illumina [7724607] (imputed) 1 carotene diol (2) measurement http://www.ebi.ac.uk/efo/EFO_0800171 GCST90264903 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma carotene diol (3) levels in chronic kidney disease 4,489 European ancestry individuals NA Illumina [7724798] (imputed) 1 carotene diol (3) measurement http://www.ebi.ac.uk/efo/EFO_0800172 GCST90264904 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma catechol glucuronide levels in chronic kidney disease 2,910 European ancestry individuals NA Illumina [7722272] (imputed) 0 catechol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800088 GCST90264905 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine catechol glucuronide levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723760] (imputed) 0 catechol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800088 GCST90264906 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma catechol sulfate levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723818] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90264907 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine catechol sulfate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90264908 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ceramide (d16:1/24:1, d18:1/22:1)* levels in chronic kidney disease 4,052 European ancestry individuals NA Illumina [7722707] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90264909 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamyltryptophan levels in chronic kidney disease 4,213 European ancestry individuals NA Illumina [7723530] (imputed) 0 gamma-glutamyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800671 GCST90265165 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamyltyrosine levels in chronic kidney disease 4,781 European ancestry individuals NA Illumina [7724622] (imputed) 0 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90265166 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamyltyrosine levels in chronic kidney disease 2,156 European ancestry individuals NA Illumina [7724050] (imputed) 1 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90265167 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-glutamylvaline levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724247] (imputed) 0 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90265168 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gamma-glutamylvaline levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723627] (imputed) 1 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90265169 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gamma-tocopherol/beta-tocopherol levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723725] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265170 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma genistein sulfate* levels in chronic kidney disease 434 European ancestry individuals NA Illumina [7737043] (imputed) 0 genistein sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801023 GCST90265171 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gentisate levels in chronic kidney disease 4,865 European ancestry individuals NA Illumina [7723818] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90265172 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gentisate levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724325] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90265173 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gentisic acid-5-glucoside levels in chronic kidney disease 4,395 European ancestry individuals NA Illumina [7724238] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265174 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine GlcNAc sulfate conjugate of C21H34O2 steroid** levels in chronic kidney disease 4,609 European ancestry individuals NA Illumina [7723653] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265175 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucarate (saccharate) levels in chronic kidney disease 3,858 European ancestry individuals NA Illumina [7723015] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265176 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gluconate levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724600] (imputed) 1 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90265177 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gluconate levels in chronic kidney disease 4,891 European ancestry individuals NA Illumina [7724610] (imputed) 1 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90265178 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucosaminate levels in chronic kidney disease 4,665 European ancestry individuals NA Illumina [7723581] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265179 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucose levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723819] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90265180 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucose levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723716] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90265181 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90265182 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronate levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723548] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90265183 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H14O2 (2)* levels in chronic kidney disease 4,684 European ancestry individuals NA Illumina [7724976] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265184 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of C10H18O2 (1)* levels in chronic kidney disease 2,231 European ancestry individuals NA Illumina [7725068] (imputed) 0 glucuronide of C10H18O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800650 GCST90265185 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (1)* levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724615] (imputed) 0 glucuronide of C10H18O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800650 GCST90265186 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (10)* levels in chronic kidney disease 4,697 European ancestry individuals NA Illumina [7724245] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265187 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (11)* levels in chronic kidney disease 4,864 European ancestry individuals NA Illumina [7724104] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265188 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (12)* levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723570] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265189 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (2)* levels in chronic kidney disease 3,876 European ancestry individuals NA Illumina [7723820] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265190 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of C10H18O2 (3)* levels in chronic kidney disease 1,094 European ancestry individuals NA Illumina [7729096] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265191 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (3)* levels in chronic kidney disease 4,797 European ancestry individuals NA Illumina [7724075] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265192 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of C10H18O2 (4)* levels in chronic kidney disease 992 European ancestry individuals NA Illumina [7731275] (imputed) 0 glucuronide of C10H18O2 (4) measurement http://www.ebi.ac.uk/efo/EFO_0800651 GCST90265193 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (4)* levels in chronic kidney disease 4,742 European ancestry individuals NA Illumina [7724008] (imputed) 0 glucuronide of C10H18O2 (4) measurement http://www.ebi.ac.uk/efo/EFO_0800651 GCST90265194 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of C10H18O2 (5)* levels in chronic kidney disease 916 European ancestry individuals NA Illumina [7723147] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265195 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (5)* levels in chronic kidney disease 4,830 European ancestry individuals NA Illumina [7724143] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265196 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of C10H18O2 (6)* levels in chronic kidney disease 1,169 European ancestry individuals NA Illumina [7724366] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265197 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (6)* levels in chronic kidney disease 3,288 European ancestry individuals NA Illumina [7724119] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265198 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of C10H18O2 (7)* levels in chronic kidney disease 4,064 European ancestry individuals NA Illumina [7722951] (imputed) 0 glucuronide of C10H18O2 (7) measurement http://www.ebi.ac.uk/efo/EFO_0800652 GCST90265199 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (7)* levels in chronic kidney disease 4,889 European ancestry individuals NA Illumina [7724070] (imputed) 0 glucuronide of C10H18O2 (7) measurement http://www.ebi.ac.uk/efo/EFO_0800652 GCST90265200 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glucuronide of C10H18O2 (8)* levels in chronic kidney disease 2,540 European ancestry individuals NA Illumina [7726006] (imputed) 0 glucuronide of C10H18O2 (8) measurement http://www.ebi.ac.uk/efo/EFO_0800653 GCST90265201 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (8)* levels in chronic kidney disease 4,728 European ancestry individuals NA Illumina [7723977] (imputed) 0 glucuronide of C10H18O2 (8) measurement http://www.ebi.ac.uk/efo/EFO_0800653 GCST90265202 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C10H18O2 (9)* levels in chronic kidney disease 4,185 European ancestry individuals NA Illumina [7723350] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265203 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H20O3 (1)* levels in chronic kidney disease 4,812 European ancestry individuals NA Illumina [7723531] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265204 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H20O3 (2)* levels in chronic kidney disease 4,440 European ancestry individuals NA Illumina [7723916] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265205 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H20O3 (3)* levels in chronic kidney disease 4,100 European ancestry individuals NA Illumina [7723329] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265206 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H20O3 (4)* levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723652] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265207 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H20O3 (5)* levels in chronic kidney disease 4,633 European ancestry individuals NA Illumina [7723972] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265208 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H22O3 (1)* levels in chronic kidney disease 4,433 European ancestry individuals NA Illumina [7724017] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265209 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H22O4 (1)* levels in chronic kidney disease 4,889 European ancestry individuals NA Illumina [7724545] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265210 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C12H22O4 (2)* levels in chronic kidney disease 4,857 European ancestry individuals NA Illumina [7723391] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265211 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glucuronide of C14H22O4 (2)* levels in chronic kidney disease 4,795 European ancestry individuals NA Illumina [7724580] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265212 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hypoxanthine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90265377 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ibuprofen acyl glucuronide levels in chronic kidney disease 1,763 European ancestry individuals NA Illumina [7723124] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265378 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24336 levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7723998] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266676 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24337 levels in chronic kidney disease 4,843 European ancestry individuals NA Illumina [7724529] (imputed) 1 X-24337 measurement http://www.ebi.ac.uk/efo/EFO_0800875 GCST90266677 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24337 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723732] (imputed) 0 X-24337 measurement http://www.ebi.ac.uk/efo/EFO_0800875 GCST90266678 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24338 levels in chronic kidney disease 4,888 European ancestry individuals NA Illumina [7724634] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266679 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24339 levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723499] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266680 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24340 levels in chronic kidney disease 4,756 European ancestry individuals NA Illumina [7723784] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266681 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24341 levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723718] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266682 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24342 levels in chronic kidney disease 4,858 European ancestry individuals NA Illumina [7723487] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266683 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24344 levels in chronic kidney disease 3,851 European ancestry individuals NA Illumina [7722922] (imputed) 0 X-24344 measurement http://www.ebi.ac.uk/efo/EFO_0800876 GCST90266684 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24344 levels in chronic kidney disease 4,531 European ancestry individuals NA Illumina [7723100] (imputed) 0 X-24344 measurement http://www.ebi.ac.uk/efo/EFO_0800876 GCST90266685 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24345 levels in chronic kidney disease 4,895 European ancestry individuals NA Illumina [7724088] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266686 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24346 levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723561] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266687 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24349 levels in chronic kidney disease 4,619 European ancestry individuals NA Illumina [7723943] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266688 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24352 levels in chronic kidney disease 1,894 European ancestry individuals NA Illumina [7726832] (imputed) 0 X-24352 measurement http://www.ebi.ac.uk/efo/EFO_0800877 GCST90266689 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24352 levels in chronic kidney disease 4,820 European ancestry individuals NA Illumina [7723982] (imputed) 0 X-24352 measurement http://www.ebi.ac.uk/efo/EFO_0800877 GCST90266690 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24353 levels in chronic kidney disease 4,843 European ancestry individuals NA Illumina [7723883] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266691 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24354 levels in chronic kidney disease 4,713 European ancestry individuals NA Illumina [7722759] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266692 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24356 levels in chronic kidney disease 3,827 European ancestry individuals NA Illumina [7723719] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266693 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24357 levels in chronic kidney disease 4,212 European ancestry individuals NA Illumina [7723317] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266694 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24359 levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723724] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266695 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24363 levels in chronic kidney disease 4,499 European ancestry individuals NA Illumina [7724748] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266696 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24387 levels in chronic kidney disease 4,886 European ancestry individuals NA Illumina [7724190] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266697 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24400 levels in chronic kidney disease 3,083 European ancestry individuals NA Illumina [7722567] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266698 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24403 levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723565] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266699 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24406 levels in chronic kidney disease 4,849 European ancestry individuals NA Illumina [7724122] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266700 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24408 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723615] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266701 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24410 levels in chronic kidney disease 3,254 European ancestry individuals NA Illumina [7721973] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266702 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24410 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266703 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24411 levels in chronic kidney disease 4,757 European ancestry individuals NA Illumina [7722903] (imputed) 0 X-24411 measurement http://www.ebi.ac.uk/efo/EFO_0800878 GCST90266704 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24411 levels in chronic kidney disease 4,806 European ancestry individuals NA Illumina [7723174] (imputed) 0 X-24411 measurement http://www.ebi.ac.uk/efo/EFO_0800878 GCST90266705 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24412 levels in chronic kidney disease 4,574 European ancestry individuals NA Illumina [7723965] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266706 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24414 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723575] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266707 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24415 levels in chronic kidney disease 4,753 European ancestry individuals NA Illumina [7722985] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266708 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24417 levels in chronic kidney disease 4,473 European ancestry individuals NA Illumina [7723412] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266709 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24418 levels in chronic kidney disease 3,202 European ancestry individuals NA Illumina [7722960] (imputed) 2 X-24418 measurement http://www.ebi.ac.uk/efo/EFO_0800879 GCST90266710 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24418 levels in chronic kidney disease 4,849 European ancestry individuals NA Illumina [7724375] (imputed) 2 X-24418 measurement http://www.ebi.ac.uk/efo/EFO_0800879 GCST90266711 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24419 levels in chronic kidney disease 3,841 European ancestry individuals NA Illumina [7724331] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266712 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24422 levels in chronic kidney disease 4,925 European ancestry individuals NA Illumina [7723908] (imputed) 1 X-24422 measurement http://www.ebi.ac.uk/efo/EFO_0800880 GCST90266713 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24422 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723581] (imputed) 0 X-24422 measurement http://www.ebi.ac.uk/efo/EFO_0800880 GCST90266714 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24425 levels in chronic kidney disease 4,842 European ancestry individuals NA Illumina [7724262] (imputed) 0 X-24425 measurement http://www.ebi.ac.uk/efo/EFO_0800881 GCST90266715 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24431 levels in chronic kidney disease 4,748 European ancestry individuals NA Illumina [7723920] (imputed) 0 X-24431 measurement http://www.ebi.ac.uk/efo/EFO_0800882 GCST90266716 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24431 levels in chronic kidney disease 4,788 European ancestry individuals NA Illumina [7723891] (imputed) 0 X-24431 measurement http://www.ebi.ac.uk/efo/EFO_0800882 GCST90266717 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24432 levels in chronic kidney disease 3,894 European ancestry individuals NA Illumina [7722104] (imputed) 0 X-24432 measurement http://www.ebi.ac.uk/efo/EFO_0800883 GCST90266718 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24432 levels in chronic kidney disease 4,458 European ancestry individuals NA Illumina [7722651] (imputed) 0 X-24432 measurement http://www.ebi.ac.uk/efo/EFO_0800883 GCST90266719 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24455 levels in chronic kidney disease 4,775 European ancestry individuals NA Illumina [7724237] (imputed) 1 X-24455 measurement http://www.ebi.ac.uk/efo/EFO_0800884 GCST90266720 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24456 levels in chronic kidney disease 4,690 European ancestry individuals NA Illumina [7724563] (imputed) 0 X-24456 measurement http://www.ebi.ac.uk/efo/EFO_0800885 GCST90266721 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24456 levels in chronic kidney disease 4,838 European ancestry individuals NA Illumina [7724952] (imputed) 0 X-24456 measurement http://www.ebi.ac.uk/efo/EFO_0800885 GCST90266722 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24457 levels in chronic kidney disease 3,296 European ancestry individuals NA Illumina [7722070] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266723 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24457 levels in chronic kidney disease 4,820 European ancestry individuals NA Illumina [7723333] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266724 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24460 levels in chronic kidney disease 4,849 European ancestry individuals NA Illumina [7724314] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266725 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23587 levels in chronic kidney disease 4,853 European ancestry individuals NA Illumina [7723075] (imputed) 0 X-23587 measurement http://www.ebi.ac.uk/efo/EFO_0800849 GCST90266601 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23587 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723586] (imputed) 0 X-23587 measurement http://www.ebi.ac.uk/efo/EFO_0800849 GCST90266602 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23593 levels in chronic kidney disease 4,939 European ancestry individuals NA Illumina [7724815] (imputed) 0 X-23593 measurement http://www.ebi.ac.uk/efo/EFO_0800851 GCST90266603 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23593 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-23593 measurement http://www.ebi.ac.uk/efo/EFO_0800851 GCST90266604 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23636 levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724214] (imputed) 2 X-23636 measurement http://www.ebi.ac.uk/efo/EFO_0800852 GCST90266605 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23639 levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723898] (imputed) 0 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90266606 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23639 levels in chronic kidney disease 4,855 European ancestry individuals NA Illumina [7723385] (imputed) 0 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90266607 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23641 levels in chronic kidney disease 4,666 European ancestry individuals NA Illumina [7722952] (imputed) 2 X-23641 measurement http://www.ebi.ac.uk/efo/EFO_0800854 GCST90266608 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23641 levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724395] (imputed) 1 X-23641 measurement http://www.ebi.ac.uk/efo/EFO_0800854 GCST90266609 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23644 levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7724127] (imputed) 0 X-23644 measurement http://www.ebi.ac.uk/efo/EFO_0800855 GCST90266610 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23644 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723596] (imputed) 0 X-23644 measurement http://www.ebi.ac.uk/efo/EFO_0800855 GCST90266611 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23645 levels in chronic kidney disease 4,711 European ancestry individuals NA Illumina [7723207] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266612 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23647 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723545] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266613 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23648 levels in chronic kidney disease 4,239 European ancestry individuals NA Illumina [7724952] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266614 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23648 levels in chronic kidney disease 4,882 European ancestry individuals NA Illumina [7724103] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266615 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23650 levels in chronic kidney disease 2,620 European ancestry individuals NA Illumina [7722399] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266616 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23652 levels in chronic kidney disease 407 European ancestry individuals NA Illumina [7709391] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266617 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23653 levels in chronic kidney disease 4,851 European ancestry individuals NA Illumina [7723377] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266618 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23654 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266619 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23655 levels in chronic kidney disease 4,464 European ancestry individuals NA Illumina [7723836] (imputed) 0 X-23655 measurement http://www.ebi.ac.uk/efo/EFO_0800856 GCST90266620 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23655 levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724791] (imputed) 0 X-23655 measurement http://www.ebi.ac.uk/efo/EFO_0800856 GCST90266621 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23656 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723555] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266622 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23657 levels in chronic kidney disease 4,779 European ancestry individuals NA Illumina [7723855] (imputed) 0 X-23657 measurement http://www.ebi.ac.uk/efo/EFO_0800857 GCST90266623 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23659 levels in chronic kidney disease 4,808 European ancestry individuals NA Illumina [7723526] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266624 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23659 levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723522] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266625 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22143 levels in chronic kidney disease 4,486 European ancestry individuals NA Illumina [7724281] (imputed) 0 X-22143 measurement http://www.ebi.ac.uk/efo/EFO_0800838 GCST90266551 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22148 levels in chronic kidney disease 3,500 European ancestry individuals NA Illumina [7724958] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266552 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22152 levels in chronic kidney disease 4,530 European ancestry individuals NA Illumina [7724027] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266553 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22158 levels in chronic kidney disease 4,573 European ancestry individuals NA Illumina [7723953] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266554 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-22162 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90266555 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22162 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723633] (imputed) 2 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90266556 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22508 levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724501] (imputed) 0 X-22508 measurement http://www.ebi.ac.uk/efo/EFO_0800840 GCST90266557 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-22509 levels in chronic kidney disease 2,460 European ancestry individuals NA Illumina [7719929] (imputed) 0 X-22509 measurement http://www.ebi.ac.uk/efo/EFO_0800841 GCST90266558 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22509 levels in chronic kidney disease 4,627 European ancestry individuals NA Illumina [7723529] (imputed) 0 X-22509 measurement http://www.ebi.ac.uk/efo/EFO_0800841 GCST90266559 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22512 levels in chronic kidney disease 3,912 European ancestry individuals NA Illumina [7722825] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266560 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22513 levels in chronic kidney disease 3,398 European ancestry individuals NA Illumina [7724500] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266561 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22520 levels in chronic kidney disease 3,059 European ancestry individuals NA Illumina [7720207] (imputed) 0 X-22520 measurement http://www.ebi.ac.uk/efo/EFO_0800843 GCST90266562 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22755 levels in chronic kidney disease 4,838 European ancestry individuals NA Illumina [7724641] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266563 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22757 levels in chronic kidney disease 4,716 European ancestry individuals NA Illumina [7723208] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266564 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-22771 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 X-22771 measurement http://www.ebi.ac.uk/efo/EFO_0800844 GCST90266565 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-22776 levels in chronic kidney disease 4,925 European ancestry individuals NA Illumina [7724202] (imputed) 0 X-22776 measurement http://www.ebi.ac.uk/efo/EFO_0800845 GCST90266566 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-22834 levels in chronic kidney disease 3,177 European ancestry individuals NA Illumina [7723776] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266567 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-22834 levels in chronic kidney disease 3,841 European ancestry individuals NA Illumina [7724396] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266568 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23039 levels in chronic kidney disease 400 European ancestry individuals NA Illumina [7727259] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266569 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23048 levels in chronic kidney disease 4,374 European ancestry individuals NA Illumina [7723808] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266570 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23157 levels in chronic kidney disease 1,129 European ancestry individuals NA Illumina [7728468] (imputed) 0 X-23157 measurement http://www.ebi.ac.uk/efo/EFO_0800846 GCST90266571 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23157 levels in chronic kidney disease 4,291 European ancestry individuals NA Illumina [7724635] (imputed) 0 X-23157 measurement http://www.ebi.ac.uk/efo/EFO_0800846 GCST90266572 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23161 levels in chronic kidney disease 4,891 European ancestry individuals NA Illumina [7724233] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266573 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23188 levels in chronic kidney disease 4,680 European ancestry individuals NA Illumina [7723755] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266574 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23276 levels in chronic kidney disease 760 European ancestry individuals NA Illumina [7717245] (imputed) 0 X-23276 measurement http://www.ebi.ac.uk/efo/EFO_0800847 GCST90266575 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23787 levels in chronic kidney disease 4,116 European ancestry individuals NA Illumina [7722492] (imputed) 2 X-23787 measurement http://www.ebi.ac.uk/efo/EFO_0800866 GCST90266651 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23868 levels in chronic kidney disease 2,390 European ancestry individuals NA Illumina [7725743] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266652 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23890 levels in chronic kidney disease 3,820 European ancestry individuals NA Illumina [7723159] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266653 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23906 levels in chronic kidney disease 3,150 European ancestry individuals NA Illumina [7723359] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266654 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23908 levels in chronic kidney disease 4,828 European ancestry individuals NA Illumina [7724198] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266655 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23974 levels in chronic kidney disease 3,547 European ancestry individuals NA Illumina [7724415] (imputed) 0 X-23974 measurement http://www.ebi.ac.uk/efo/EFO_0800867 GCST90266656 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23983 levels in chronic kidney disease 4,460 European ancestry individuals NA Illumina [7723459] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266657 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23984 levels in chronic kidney disease 4,931 European ancestry individuals NA Illumina [7724294] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266658 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23997 levels in chronic kidney disease 4,850 European ancestry individuals NA Illumina [7723670] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90266659 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23997 levels in chronic kidney disease 4,774 European ancestry individuals NA Illumina [7724056] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90266660 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24216 levels in chronic kidney disease 808 European ancestry individuals NA Illumina [7719380] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266661 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24228 levels in chronic kidney disease 4,121 European ancestry individuals NA Illumina [7723400] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266662 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24241 levels in chronic kidney disease 3,457 European ancestry individuals NA Illumina [7722552] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266663 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24246 levels in chronic kidney disease 4,086 European ancestry individuals NA Illumina [7725252] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266664 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24249 levels in chronic kidney disease 4,507 European ancestry individuals NA Illumina [7723551] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266665 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24270 levels in chronic kidney disease 4,587 European ancestry individuals NA Illumina [7725530] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266666 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24295 levels in chronic kidney disease 4,672 European ancestry individuals NA Illumina [7723689] (imputed) 0 X-24295 measurement http://www.ebi.ac.uk/efo/EFO_0800869 GCST90266667 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24307 levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724214] (imputed) 0 X-24307 measurement http://www.ebi.ac.uk/efo/EFO_0800871 GCST90266668 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24327 levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723819] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266669 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24328 levels in chronic kidney disease 4,185 European ancestry individuals NA Illumina [7723250] (imputed) 0 X-24328 measurement http://www.ebi.ac.uk/efo/EFO_0800873 GCST90266670 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24328 levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723663] (imputed) 0 X-24328 measurement http://www.ebi.ac.uk/efo/EFO_0800873 GCST90266671 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24330 levels in chronic kidney disease 4,876 European ancestry individuals NA Illumina [7724126] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266672 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24332 levels in chronic kidney disease 4,797 European ancestry individuals NA Illumina [7724850] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266673 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24333 levels in chronic kidney disease 4,795 European ancestry individuals NA Illumina [7724008] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266674 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24334 levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723614] (imputed) 1 X-24334 measurement http://www.ebi.ac.uk/efo/EFO_0800874 GCST90266675 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23662 levels in chronic kidney disease 2,422 European ancestry individuals NA Illumina [7723660] (imputed) 0 X-23662 measurement http://www.ebi.ac.uk/efo/EFO_0800858 GCST90266626 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23662 levels in chronic kidney disease 4,738 European ancestry individuals NA Illumina [7724019] (imputed) 0 X-23662 measurement http://www.ebi.ac.uk/efo/EFO_0800858 GCST90266627 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23665 levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7723966] (imputed) 0 X-23665 measurement http://www.ebi.ac.uk/efo/EFO_0800859 GCST90266628 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23665 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723478] (imputed) 0 X-23665 measurement http://www.ebi.ac.uk/efo/EFO_0800859 GCST90266629 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23666 levels in chronic kidney disease 4,320 European ancestry individuals NA Illumina [7724415] (imputed) 0 X-23666 measurement http://www.ebi.ac.uk/efo/EFO_0800860 GCST90266630 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23666 levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724461] (imputed) 0 X-23666 measurement http://www.ebi.ac.uk/efo/EFO_0800860 GCST90266631 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23668 levels in chronic kidney disease 4,100 European ancestry individuals NA Illumina [7725405] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266632 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23671 levels in chronic kidney disease 484 European ancestry individuals NA Illumina [7739863] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266633 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23671 levels in chronic kidney disease 547 European ancestry individuals NA Illumina [7744282] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266634 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23672 levels in chronic kidney disease 4,800 European ancestry individuals NA Illumina [7723965] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266635 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23674 levels in chronic kidney disease 473 European ancestry individuals NA Illumina [7728702] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266636 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23678 levels in chronic kidney disease 3,066 European ancestry individuals NA Illumina [7720815] (imputed) 0 X-23678 measurement http://www.ebi.ac.uk/efo/EFO_0800861 GCST90266637 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23678 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-23678 measurement http://www.ebi.ac.uk/efo/EFO_0800861 GCST90266638 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23680 levels in chronic kidney disease 4,934 European ancestry individuals NA Illumina [7724326] (imputed) 1 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90266639 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23680 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723511] (imputed) 1 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90266640 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23738 levels in chronic kidney disease 4,756 European ancestry individuals NA Illumina [7723572] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266641 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23739 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90266642 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23739 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90266643 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23748 levels in chronic kidney disease 4,663 European ancestry individuals NA Illumina [7724280] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266644 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23748 levels in chronic kidney disease 4,894 European ancestry individuals NA Illumina [7724250] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266645 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23775 levels in chronic kidney disease 338 European ancestry individuals NA Illumina [7746124] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266646 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23780 levels in chronic kidney disease 4,880 European ancestry individuals NA Illumina [7724137] (imputed) 1 X-23780 measurement http://www.ebi.ac.uk/efo/EFO_0800864 GCST90266647 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23780 levels in chronic kidney disease 4,838 European ancestry individuals NA Illumina [7724457] (imputed) 0 X-23780 measurement http://www.ebi.ac.uk/efo/EFO_0800864 GCST90266648 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23782 levels in chronic kidney disease 4,878 European ancestry individuals NA Illumina [7723663] (imputed) 0 X-23782 measurement http://www.ebi.ac.uk/efo/EFO_0800865 GCST90266649 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23787 levels in chronic kidney disease 3,585 European ancestry individuals NA Illumina [7722775] (imputed) 0 X-23787 measurement http://www.ebi.ac.uk/efo/EFO_0800866 GCST90266650 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23299 levels in chronic kidney disease 4,034 European ancestry individuals NA Illumina [7724575] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266576 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23304 levels in chronic kidney disease 4,867 European ancestry individuals NA Illumina [7723577] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266577 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23311 levels in chronic kidney disease 2,991 European ancestry individuals NA Illumina [7725132] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266578 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23329 levels in chronic kidney disease 2,894 European ancestry individuals NA Illumina [7722216] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266579 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23329 levels in chronic kidney disease 4,723 European ancestry individuals NA Illumina [7723726] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266580 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23331 levels in chronic kidney disease 4,779 European ancestry individuals NA Illumina [7724126] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266581 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23423 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723452] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266582 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23424 levels in chronic kidney disease 3,203 European ancestry individuals NA Illumina [7721706] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266583 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23429 levels in chronic kidney disease 4,769 European ancestry individuals NA Illumina [7723729] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266584 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23436 levels in chronic kidney disease 3,708 European ancestry individuals NA Illumina [7722960] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266585 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23438 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723627] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266586 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23459 levels in chronic kidney disease 4,772 European ancestry individuals NA Illumina [7724019] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266587 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23481 levels in chronic kidney disease 2,452 European ancestry individuals NA Illumina [7720991] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266588 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23481 levels in chronic kidney disease 1,459 European ancestry individuals NA Illumina [7722117] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266589 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23482 levels in chronic kidney disease 4,850 European ancestry individuals NA Illumina [7724334] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266590 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23502 levels in chronic kidney disease 4,520 European ancestry individuals NA Illumina [7723593] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266591 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23511 levels in chronic kidney disease 2,644 European ancestry individuals NA Illumina [7726353] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266592 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23512 levels in chronic kidney disease 1,774 European ancestry individuals NA Illumina [7727066] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266593 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23517 levels in chronic kidney disease 4,584 European ancestry individuals NA Illumina [7724382] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266594 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23518 levels in chronic kidney disease 4,190 European ancestry individuals NA Illumina [7723553] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266595 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23581 levels in chronic kidney disease 3,040 European ancestry individuals NA Illumina [7725045] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266596 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23581 levels in chronic kidney disease 4,709 European ancestry individuals NA Illumina [7723738] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266597 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-23583 levels in chronic kidney disease 3,338 European ancestry individuals NA Illumina [7723856] (imputed) 0 X-23583 measurement http://www.ebi.ac.uk/efo/EFO_0800848 GCST90266598 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23583 levels in chronic kidney disease 4,708 European ancestry individuals NA Illumina [7723081] (imputed) 0 X-23583 measurement http://www.ebi.ac.uk/efo/EFO_0800848 GCST90266599 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-23584 levels in chronic kidney disease 807 European ancestry individuals NA Illumina [7715038] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266600 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma aspartate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90264837 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine aspartate levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723560] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90264838 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma azelate (C9-DC) levels in chronic kidney disease 4,706 European ancestry individuals NA Illumina [7723473] (imputed) 0 azelate (C9-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800615 GCST90264839 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine azelate (C9-DC) levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724058] (imputed) 1 azelate (C9-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800615 GCST90264840 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine azeloylcarnitine (C9-DC) levels in chronic kidney disease 1,220 European ancestry individuals NA Illumina [7723805] (imputed) 0 azelate (C9-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800615 GCST90264841 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma behenoyl dihydrosphingomyelin (d18:0/22:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 behenoyl dihydrosphingomyelin (d18:0/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800427 GCST90264842 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma behenoyl sphingomyelin (d18:1/22:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 behenoyl sphingomyelin (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800376 GCST90264843 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma behenoylcarnitine (C22)* levels in chronic kidney disease 3,305 European ancestry individuals NA Illumina [7723802] (imputed) 1 behenoylcarnitine (C22) measurement http://www.ebi.ac.uk/efo/EFO_0800539 GCST90264844 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine benzoate levels in chronic kidney disease 4,005 European ancestry individuals NA Illumina [7723073] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90264845 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma benzoylcarnitine* levels in chronic kidney disease 4,027 European ancestry individuals NA Illumina [7723746] (imputed) 0 benzoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800986 GCST90264846 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine benzoylcarnitine* levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723635] (imputed) 0 benzoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800986 GCST90264847 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma beta-alanine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0800640 GCST90264848 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine beta-alanine levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7723836] (imputed) 1 beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0800640 GCST90264849 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma beta-citrylglutamate levels in chronic kidney disease 4,927 European ancestry individuals NA Illumina [7723906] (imputed) 1 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90264850 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine beta-citrylglutamate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90264851 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma beta-cryptoxanthin levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724090] (imputed) 0 cryptoxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007897 GCST90264852 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine beta-guanidinopropanoate levels in chronic kidney disease 2,839 European ancestry individuals NA Illumina [7725326] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264853 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma beta-hydroxyisovalerate levels in chronic kidney disease 4,479 European ancestry individuals NA Illumina [7723723] (imputed) 3 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90264854 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine beta-hydroxyisovalerate levels in chronic kidney disease 4,858 European ancestry individuals NA Illumina [7723425] (imputed) 0 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90264855 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma beta-hydroxyisovaleroylcarnitine levels in chronic kidney disease 4,849 European ancestry individuals NA Illumina [7723812] (imputed) 1 beta-hydroxyisovaleroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800031 GCST90264856 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine beta-hydroxyisovaleroylcarnitine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 beta-hydroxyisovaleroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800031 GCST90264857 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma betaine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 4 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90264858 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin (E,Z or Z,E)* levels in chronic kidney disease 4,656 European ancestry individuals NA Illumina [7723817] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264862 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma bilirubin (Z,Z) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723901] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90264863 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dimethylarginine (SDMA + ADMA) levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90265043 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycolate (hydroxyacetate) levels in chronic kidney disease 3,446 European ancestry individuals NA Illumina [7724273] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265298 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycolithocholate levels in chronic kidney disease 3,342 European ancestry individuals NA Illumina [7723417] (imputed) 0 glycolithocholate measurement http://www.ebi.ac.uk/efo/EFO_0800203 GCST90265299 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycolithocholate sulfate* levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723371] (imputed) 1 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90265300 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycolithocholate sulfate* levels in chronic kidney disease 4,779 European ancestry individuals NA Illumina [7723747] (imputed) 1 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90265301 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycosyl ceramide (d18:1/20:0, d16:1/22:0)* levels in chronic kidney disease 4,935 European ancestry individuals NA Illumina [7724128] (imputed) 2 glycosyl ceramide (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800551 GCST90265302 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycosyl ceramide (d18:2/24:1, d18:1/24:2)* levels in chronic kidney disease 4,916 European ancestry individuals NA Illumina [7724019] (imputed) 1 glycosyl ceramide (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0800532 GCST90265303 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH))* levels in chronic kidney disease 4,751 European ancestry individuals NA Illumina [7723811] (imputed) 2 glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800533 GCST90265304 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycosyl-N-behenoyl-sphingadienine (d18:2/22:0)* levels in chronic kidney disease 4,843 European ancestry individuals NA Illumina [7724925] (imputed) 1 glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800520 GCST90265305 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800476 GCST90265306 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels in chronic kidney disease 4,941 European ancestry individuals NA Illumina [7724632] (imputed) 2 glycosyl-N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800275 GCST90265307 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycoursodeoxycholate levels in chronic kidney disease 4,935 European ancestry individuals NA Illumina [7724237] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90265308 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycoursodeoxycholate levels in chronic kidney disease 3,079 European ancestry individuals NA Illumina [7724905] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90265309 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycoursodeoxycholic acid sulfate (1) levels in chronic kidney disease 3,790 European ancestry individuals NA Illumina [7723677] (imputed) 1 glycoursodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800578 GCST90265310 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycoursodeoxycholic acid sulfate (1) levels in chronic kidney disease 1,621 European ancestry individuals NA Illumina [7724280] (imputed) 0 glycoursodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800578 GCST90265311 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma guaiacol sulfate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 guaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800978 GCST90265312 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine guaiacol sulfate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 guaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800978 GCST90265313 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma guanidinoacetate levels in chronic kidney disease 4,940 European ancestry individuals NA Illumina [7724460] (imputed) 0 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90265314 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine guanidinoacetate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723576] (imputed) 0 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90265315 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine guanidinosuccinate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723579] (imputed) 0 guanidinosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800016 GCST90265316 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine guanine levels in chronic kidney disease 4,793 European ancestry individuals NA Illumina [7724327] (imputed) 0 guanine measurement http://www.ebi.ac.uk/efo/EFO_0801165 GCST90265317 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine guanosine levels in chronic kidney disease 2,123 European ancestry individuals NA Illumina [7723483] (imputed) 1 guanosine measurement http://www.ebi.ac.uk/efo/EFO_0021124 GCST90265318 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine guanosine-3',5'-cyclic monophosphate (cGMP) levels in chronic kidney disease 4,177 European ancestry individuals NA Illumina [7723949] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265319 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma gulonate* levels in chronic kidney disease 4,794 European ancestry individuals NA Illumina [7724897] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90265320 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine gulonate* levels in chronic kidney disease 4,878 European ancestry individuals NA Illumina [7723970] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90265321 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma heneicosapentaenoate (21:5n3) levels in chronic kidney disease 1,221 European ancestry individuals NA Illumina [7727652] (imputed) 0 heneicosapentaenoate (21:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800537 GCST90265322 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dimethylglycine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90265044 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dimethylglycine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90265045 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dimethylmalonic acid levels in chronic kidney disease 4,836 European ancestry individuals NA Illumina [7724008] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265046 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma docosadienoate (22:2n6) levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723894] (imputed) 0 docosadienoate (22:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800211 GCST90265047 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma docosadioate (C22-DC) levels in chronic kidney disease 4,689 European ancestry individuals NA Illumina [7723722] (imputed) 0 docosadioate (C22-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800331 GCST90265048 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma docosahexaenoate (DHA; 22:6n3) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 docosahexaenoate DHA; 22:6n3 measurement http://www.ebi.ac.uk/efo/EFO_0021047 GCST90265049 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma docosahexaenoylcholine levels in chronic kidney disease 4,571 European ancestry individuals NA Illumina [7724097] (imputed) 0 docosahexaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800479 GCST90265050 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma docosapentaenoate (n3 DPA; 22:5n3) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723735] (imputed) 1 docosapentaenoate n3 DPA; 22:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021048 GCST90265051 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma docosapentaenoate (n6 DPA; 22:5n6) levels in chronic kidney disease 4,898 European ancestry individuals NA Illumina [7724473] (imputed) 0 docosapentaenoate (n6 DPA; 22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800249 GCST90265052 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma docosatrienoate (22:3n6)* levels in chronic kidney disease 3,631 European ancestry individuals NA Illumina [7722562] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265053 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dodecadienoate (12:2)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 dodecadienoate (12:2) measurement http://www.ebi.ac.uk/efo/EFO_0800572 GCST90265054 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dodecanedioate (C12-DC) levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724555] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265055 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dodecenedioate (C12:1-DC)* levels in chronic kidney disease 4,194 European ancestry individuals NA Illumina [7723891] (imputed) 0 dodecenedioate (C12:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800561 GCST90265056 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dopamine 3-O-sulfate levels in chronic kidney disease 4,948 European ancestry individuals NA Illumina [7724597] (imputed) 0 dopamine 3-O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800082 GCST90265057 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dopamine 3-O-sulfate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723594] (imputed) 0 dopamine 3-O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800082 GCST90265058 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dopamine 4-sulfate levels in chronic kidney disease 2,964 European ancestry individuals NA Illumina [7722333] (imputed) 0 dopamine 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800081 GCST90265059 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dopamine 4-sulfate levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723544] (imputed) 0 dopamine 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800081 GCST90265060 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dopamine levels in chronic kidney disease 4,857 European ancestry individuals NA Illumina [7723963] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265061 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ectoine levels in chronic kidney disease 4,657 European ancestry individuals NA Illumina [7723968] (imputed) 0 ectoine measurement http://www.ebi.ac.uk/efo/EFO_0800953 GCST90265062 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ectoine levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723597] (imputed) 0 ectoine measurement http://www.ebi.ac.uk/efo/EFO_0800953 GCST90265063 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma EDTA levels in chronic kidney disease 4,946 European ancestry individuals NA Illumina [7724809] (imputed) 0 EDTA measurement http://www.ebi.ac.uk/efo/EFO_0800946 GCST90265064 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosadienamide (20:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265065 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosanedioate (C20-DC) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 eicosanedioate (C20-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800330 GCST90265066 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosapentaenoate (EPA; 20:5n3) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 eicosapentaenoate (EPA; 20:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800616 GCST90265067 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosapentaenoylcholine levels in chronic kidney disease 3,193 European ancestry individuals NA Illumina [7723180] (imputed) 0 eicosapentaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800482 GCST90265068 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosenamide (20:1)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265069 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosenedioate (C20:1-DC)* levels in chronic kidney disease 4,552 European ancestry individuals NA Illumina [7724437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265070 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosenoate (20:1) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 eicosenoate (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800220 GCST90265071 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eicosenoylcarnitine (C20:1)* levels in chronic kidney disease 4,834 European ancestry individuals NA Illumina [7724513] (imputed) 0 eicosenoylcarnitine (C20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800545 GCST90265072 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma enalapril levels in chronic kidney disease 344 European ancestry individuals NA Illumina [7753459] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265073 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine enalapril levels in chronic kidney disease 577 European ancestry individuals NA Illumina [7728279] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265074 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma enalaprilat* levels in chronic kidney disease 342 European ancestry individuals NA Illumina [7751993] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265075 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine enterolactone sulfate levels in chronic kidney disease 4,624 European ancestry individuals NA Illumina [7723096] (imputed) 0 enterolactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801029 GCST90265076 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine enterolactone levels in chronic kidney disease 2,635 European ancestry individuals NA Illumina [7722003] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265077 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine epiandrosterone glucuronide levels in chronic kidney disease 4,570 European ancestry individuals NA Illumina [7723817] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265078 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma epiandrosterone sulfate levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724344] (imputed) 1 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90265079 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine epiandrosterone sulfate levels in chronic kidney disease 4,223 European ancestry individuals NA Illumina [7723307] (imputed) 1 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90265080 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine equol glucuronide levels in chronic kidney disease 1,381 European ancestry individuals NA Illumina [7725978] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265081 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine equol sulfate levels in chronic kidney disease 366 European ancestry individuals NA Illumina [7718721] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265082 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ergothioneine levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723824] (imputed) 1 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90265083 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ergothioneine levels in chronic kidney disease 651 European ancestry individuals NA Illumina [7719072] (imputed) 0 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90265084 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma erucate (22:1n9) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 erucate (22:1n9) measurement http://www.ebi.ac.uk/efo/EFO_0800601 GCST90265085 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma erythritol levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724354] (imputed) 0 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90265086 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine erythritol levels in chronic kidney disease 4,891 European ancestry individuals NA Illumina [7724432] (imputed) 1 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90265087 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma erythronate* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723697] (imputed) 1 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90265088 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine erythronate* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90265089 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ethyl alpha-glucopyranoside levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723328] (imputed) 0 ethyl alpha-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801019 GCST90265090 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ethyl alpha-glucopyranoside levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723567] (imputed) 0 ethyl alpha-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801019 GCST90265091 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ethyl beta-glucopyranoside levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723779] (imputed) 1 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90265092 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ethyl beta-glucopyranoside levels in chronic kidney disease 3,636 European ancestry individuals NA Illumina [7725601] (imputed) 1 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90265093 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma formiminoglutamate levels in chronic kidney disease 4,913 European ancestry individuals NA Illumina [7723944] (imputed) 0 formiminoglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800050 GCST90265119 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine formiminoglutamate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 formiminoglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800050 GCST90265120 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine fructose 1,6-diphosphate/glucose 1,6-diphosphate/myo-inositol diphosphates levels in chronic kidney disease 1,254 European ancestry individuals NA Illumina [7719059] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265121 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma fructose levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724168] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90265122 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine fructose levels in chronic kidney disease 944 European ancestry individuals NA Illumina [7729952] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90265123 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma fructosyllysine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 fructosyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800073 GCST90265124 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine fucitol levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723618] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265125 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine fucose levels in chronic kidney disease 406 European ancestry individuals NA Illumina [7708878] (imputed) 1 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90265126 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma fumarate levels in chronic kidney disease 4,943 European ancestry individuals NA Illumina [7724613] (imputed) 1 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90265127 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine fumarate levels in chronic kidney disease 4,810 European ancestry individuals NA Illumina [7723419] (imputed) 0 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90265128 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma furaneol sulfate levels in chronic kidney disease 3,919 European ancestry individuals NA Illumina [7722354] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265129 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine furaneol sulfate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723503] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265130 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma furosemide levels in chronic kidney disease 427 European ancestry individuals NA Illumina [7727742] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265131 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine furosemide levels in chronic kidney disease 499 European ancestry individuals NA Illumina [7742422] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265132 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycochenodeoxycholate levels in chronic kidney disease 1,782 European ancestry individuals NA Illumina [7724142] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90265287 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycocholate glucuronide (1) levels in chronic kidney disease 2,897 European ancestry individuals NA Illumina [7725486] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265288 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycocholate levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723873] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90265289 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycocholate levels in chronic kidney disease 3,986 European ancestry individuals NA Illumina [7725015] (imputed) 1 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90265290 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycocholenate sulfate* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723778] (imputed) 3 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90265291 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycocholenate sulfate* levels in chronic kidney disease 4,894 European ancestry individuals NA Illumina [7724350] (imputed) 2 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90265292 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycodeoxycholate 3-sulfate levels in chronic kidney disease 4,527 European ancestry individuals NA Illumina [7723675] (imputed) 3 glycodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800385 GCST90265293 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycodeoxycholate 3-sulfate levels in chronic kidney disease 4,625 European ancestry individuals NA Illumina [7723436] (imputed) 2 glycodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800385 GCST90265294 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycodeoxycholate levels in chronic kidney disease 3,187 European ancestry individuals NA Illumina [7723176] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90265295 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine glycodeoxycholate levels in chronic kidney disease 2,379 European ancestry individuals NA Illumina [7723870] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90265296 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma glycohyocholate levels in chronic kidney disease 3,287 European ancestry individuals NA Illumina [7723472] (imputed) 0 glycohyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800346 GCST90265297 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homocitrate levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723632] (imputed) 0 homocitrate measurement http://www.ebi.ac.uk/efo/EFO_0800179 GCST90265348 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma homocitrulline levels in chronic kidney disease 4,761 European ancestry individuals NA Illumina [7723792] (imputed) 1 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90265349 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homocitrulline levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724607] (imputed) 2 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90265350 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homoserine levels in chronic kidney disease 398 European ancestry individuals NA Illumina [7750622] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265351 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma homostachydrine* levels in chronic kidney disease 4,915 European ancestry individuals NA Illumina [7724149] (imputed) 1 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90265352 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homostachydrine* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90265353 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homovanillate (HVA) levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723499] (imputed) 0 HVA measurement http://www.ebi.ac.uk/efo/EFO_0005131 GCST90265354 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homovanillate sulfate levels in chronic kidney disease 1,524 European ancestry individuals NA Illumina [7722933] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265355 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma homoveratric acid levels in chronic kidney disease 2,166 European ancestry individuals NA Illumina [7722922] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265356 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine homoveratric acid levels in chronic kidney disease 1,882 European ancestry individuals NA Illumina [7725289] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265357 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydantoin-5-propionate levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724308] (imputed) 1 hydantoin-5-propionate measurement http://www.ebi.ac.uk/efo/EFO_0800051 GCST90265358 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hydantoin-5-propionate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723587] (imputed) 1 hydantoin-5-propionate measurement http://www.ebi.ac.uk/efo/EFO_0800051 GCST90265359 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydrochlorothiazide levels in chronic kidney disease 1,692 European ancestry individuals NA Illumina [7723999] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265360 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hydrochlorothiazide levels in chronic kidney disease 1,798 European ancestry individuals NA Illumina [7725141] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265361 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hydroquinone beta-D-glucopyranoside levels in chronic kidney disease 982 European ancestry individuals NA Illumina [7728866] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265362 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydroquinone sulfate levels in chronic kidney disease 4,800 European ancestry individuals NA Illumina [7724840] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90265363 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hydroquinone sulfate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723578] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90265364 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydroxy-CMPF* levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724331] (imputed) 0 hydroxy-CMPF measurement http://www.ebi.ac.uk/efo/EFO_0800557 GCST90265365 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydroxy-N6,N6,N6-trimethyllysine* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723835] (imputed) 0 hydroxy-N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800112 GCST90265366 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hydroxy-N6,N6,N6-trimethyllysine* levels in chronic kidney disease 4,894 European ancestry individuals NA Illumina [7724518] (imputed) 0 hydroxy-N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800112 GCST90265367 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydroxyasparagine** levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 hydroxyasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800092 GCST90265368 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hydroxyasparagine** levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 hydroxyasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800092 GCST90265369 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydroxycotinine levels in chronic kidney disease 1,210 European ancestry individuals NA Illumina [7726233] (imputed) 0 hydroxycotinine measurement http://www.ebi.ac.uk/efo/EFO_0800964 GCST90265370 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine hydroxycotinine levels in chronic kidney disease 993 European ancestry individuals NA Illumina [7736421] (imputed) 0 hydroxycotinine measurement http://www.ebi.ac.uk/efo/EFO_0800964 GCST90265371 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH))** levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723755] (imputed) 1 hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800583 GCST90265372 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ethyl glucuronide levels in chronic kidney disease 1,680 European ancestry individuals NA Illumina [7721396] (imputed) 0 ethyl glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800967 GCST90265094 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ethyl glucuronide levels in chronic kidney disease 2,916 European ancestry individuals NA Illumina [7720162] (imputed) 0 ethyl glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800967 GCST90265095 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ethyl maltol sulfate levels in chronic kidney disease 4,859 European ancestry individuals NA Illumina [7723726] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265096 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ethylmalonate levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723663] (imputed) 3 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90265097 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ethylmalonate levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 2 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90265098 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ethylparaben sulfate levels in chronic kidney disease 4,266 European ancestry individuals NA Illumina [7722185] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265099 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma etiocholanolone glucuronide levels in chronic kidney disease 4,627 European ancestry individuals NA Illumina [7723857] (imputed) 1 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90265100 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine etiocholanolone glucuronide levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723616] (imputed) 1 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90265101 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma eugenol sulfate levels in chronic kidney disease 4,708 European ancestry individuals NA Illumina [7722737] (imputed) 0 eugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800999 GCST90265102 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine eugenol sulfate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723601] (imputed) 0 eugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800999 GCST90265103 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ferulate levels in chronic kidney disease 1,250 European ancestry individuals NA Illumina [7722929] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265104 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ferulic acid 4-sulfate levels in chronic kidney disease 4,223 European ancestry individuals NA Illumina [7724159] (imputed) 1 ferulic acid 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800989 GCST90265105 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ferulic acid 4-sulfate levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724177] (imputed) 1 ferulic acid 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800989 GCST90265106 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma feruloylquinate (1) levels in chronic kidney disease 3,049 European ancestry individuals NA Illumina [7723935] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265107 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine feruloylquinate (1) levels in chronic kidney disease 4,348 European ancestry individuals NA Illumina [7725979] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265108 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma feruloylquinate (2) levels in chronic kidney disease 3,221 European ancestry individuals NA Illumina [7723277] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265109 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine feruloylquinate (2) levels in chronic kidney disease 4,470 European ancestry individuals NA Illumina [7724101] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265110 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine feruloylquinate (3) levels in chronic kidney disease 3,863 European ancestry individuals NA Illumina [7723866] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265111 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma feruloylquinate (4) levels in chronic kidney disease 3,112 European ancestry individuals NA Illumina [7722806] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265112 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma feruloylquinate (5) levels in chronic kidney disease 2,637 European ancestry individuals NA Illumina [7723585] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265113 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine feruloylquinate (5) levels in chronic kidney disease 4,517 European ancestry individuals NA Illumina [7724252] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265114 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ferulylglycine (1) levels in chronic kidney disease 2,982 European ancestry individuals NA Illumina [7725341] (imputed) 0 ferulylglycine (1) measurement http://www.ebi.ac.uk/efo/EFO_0801016 GCST90265115 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ferulylglycine (1) levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723577] (imputed) 0 ferulylglycine (1) measurement http://www.ebi.ac.uk/efo/EFO_0801016 GCST90265116 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ferulylglycine (2) levels in chronic kidney disease 2,801 European ancestry individuals NA Illumina [7724233] (imputed) 0 ferulylglycine (2) measurement http://www.ebi.ac.uk/efo/EFO_0801017 GCST90265117 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine ferulylglycine (2) levels in chronic kidney disease 4,880 European ancestry individuals NA Illumina [7723738] (imputed) 0 ferulylglycine (2) measurement http://www.ebi.ac.uk/efo/EFO_0801017 GCST90265118 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-25109 levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724260] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266826 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-25164 levels in chronic kidney disease 2,157 European ancestry individuals NA Illumina [7719147] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266827 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25172 levels in chronic kidney disease 4,870 European ancestry individuals NA Illumina [7724433] (imputed) 0 X-25172 measurement http://www.ebi.ac.uk/efo/EFO_0800916 GCST90266828 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25217 levels in chronic kidney disease 2,121 European ancestry individuals NA Illumina [7721273] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266829 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25244 levels in chronic kidney disease 2,552 European ancestry individuals NA Illumina [7720696] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266830 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25265 levels in chronic kidney disease 4,923 European ancestry individuals NA Illumina [7724246] (imputed) 0 X-25265 measurement http://www.ebi.ac.uk/efo/EFO_0800917 GCST90266831 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25266 levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724214] (imputed) 0 X-25266 measurement http://www.ebi.ac.uk/efo/EFO_0800918 GCST90266832 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25267 levels in chronic kidney disease 4,926 European ancestry individuals NA Illumina [7724214] (imputed) 0 X-25267 measurement http://www.ebi.ac.uk/efo/EFO_0800919 GCST90266833 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25271 levels in chronic kidney disease 4,857 European ancestry individuals NA Illumina [7723586] (imputed) 0 X-25271 measurement http://www.ebi.ac.uk/efo/EFO_0800920 GCST90266834 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25279 levels in chronic kidney disease 2,326 European ancestry individuals NA Illumina [7724043] (imputed) 1 X-25279 measurement http://www.ebi.ac.uk/efo/EFO_0800921 GCST90266835 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25310 levels in chronic kidney disease 4,168 European ancestry individuals NA Illumina [7722731] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266836 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25343 levels in chronic kidney disease 4,944 European ancestry individuals NA Illumina [7724610] (imputed) 0 X-25343 measurement http://www.ebi.ac.uk/efo/EFO_0800922 GCST90266837 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25371 levels in chronic kidney disease 4,917 European ancestry individuals NA Illumina [7723556] (imputed) 1 X-25371 measurement http://www.ebi.ac.uk/efo/EFO_0800923 GCST90266838 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25417 levels in chronic kidney disease 3,108 European ancestry individuals NA Illumina [7722140] (imputed) 0 X-25417 measurement http://www.ebi.ac.uk/efo/EFO_0800924 GCST90266839 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25419 levels in chronic kidney disease 4,784 European ancestry individuals NA Illumina [7724314] (imputed) 1 X-25419 measurement http://www.ebi.ac.uk/efo/EFO_0800925 GCST90266840 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25420 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 X-25420 measurement http://www.ebi.ac.uk/efo/EFO_0800926 GCST90266841 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25422 levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723825] (imputed) 1 X-25422 measurement http://www.ebi.ac.uk/efo/EFO_0800927 GCST90266842 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25423 levels in chronic kidney disease 4,728 European ancestry individuals NA Illumina [7724153] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266843 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25433 levels in chronic kidney disease 2,387 European ancestry individuals NA Illumina [7724409] (imputed) 0 X-25433 measurement http://www.ebi.ac.uk/efo/EFO_0800928 GCST90266844 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25450 levels in chronic kidney disease 1,579 European ancestry individuals NA Illumina [7724088] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266845 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25519 levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723851] (imputed) 0 X-25519 measurement http://www.ebi.ac.uk/efo/EFO_0800930 GCST90266846 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25520 levels in chronic kidney disease 4,922 European ancestry individuals NA Illumina [7723518] (imputed) 0 X-25520 measurement http://www.ebi.ac.uk/efo/EFO_0800931 GCST90266847 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25668 levels in chronic kidney disease 2,873 European ancestry individuals NA Illumina [7722152] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266848 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25790 levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723710] (imputed) 0 X-25790 measurement http://www.ebi.ac.uk/efo/EFO_0800933 GCST90266849 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25802 levels in chronic kidney disease 1,802 European ancestry individuals NA Illumina [7718682] (imputed) 0 X-25802 measurement http://www.ebi.ac.uk/efo/EFO_0800935 GCST90266850 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24797 levels in chronic kidney disease 3,946 European ancestry individuals NA Illumina [7725287] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266801 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24798 levels in chronic kidney disease 4,670 European ancestry individuals NA Illumina [7723910] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266802 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24799 levels in chronic kidney disease 4,440 European ancestry individuals NA Illumina [7724015] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266803 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24801 levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723636] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266804 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24801 levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723619] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266805 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X - 24807 levels in chronic kidney disease 4,749 European ancestry individuals NA Illumina [7724282] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266806 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24808 levels in chronic kidney disease 4,023 European ancestry individuals NA Illumina [7722035] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266807 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24810 levels in chronic kidney disease 3,848 European ancestry individuals NA Illumina [7724764] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266808 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24811 levels in chronic kidney disease 4,551 European ancestry individuals NA Illumina [7724495] (imputed) 0 X-24811 measurement http://www.ebi.ac.uk/efo/EFO_0800907 GCST90266809 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24811 levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7724397] (imputed) 0 X-24811 measurement http://www.ebi.ac.uk/efo/EFO_0800907 GCST90266810 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24812 levels in chronic kidney disease 4,596 European ancestry individuals NA Illumina [7724266] (imputed) 0 X-24812 measurement http://www.ebi.ac.uk/efo/EFO_0800908 GCST90266811 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24812 levels in chronic kidney disease 4,830 European ancestry individuals NA Illumina [7723975] (imputed) 0 X-24812 measurement http://www.ebi.ac.uk/efo/EFO_0800908 GCST90266812 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24834 levels in chronic kidney disease 1,595 European ancestry individuals NA Illumina [7729621] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266813 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24838 levels in chronic kidney disease 1,566 European ancestry individuals NA Illumina [7724596] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266814 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24840 levels in chronic kidney disease 2,990 European ancestry individuals NA Illumina [7723266] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266815 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24947 levels in chronic kidney disease 4,615 European ancestry individuals NA Illumina [7723255] (imputed) 3 X-24947 measurement http://www.ebi.ac.uk/efo/EFO_0800910 GCST90266816 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24949 levels in chronic kidney disease 3,169 European ancestry individuals NA Illumina [7722892] (imputed) 2 X-24949 measurement http://www.ebi.ac.uk/efo/EFO_0800911 GCST90266817 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24951 levels in chronic kidney disease 3,223 European ancestry individuals NA Illumina [7722703] (imputed) 0 X-24951 measurement http://www.ebi.ac.uk/efo/EFO_0800912 GCST90266818 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24952 levels in chronic kidney disease 4,877 European ancestry individuals NA Illumina [7724083] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266819 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24971 levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723579] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266820 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24972 levels in chronic kidney disease 1,346 European ancestry individuals NA Illumina [7729665] (imputed) 0 X-24972 measurement http://www.ebi.ac.uk/efo/EFO_0800914 GCST90266821 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24975 levels in chronic kidney disease 4,014 European ancestry individuals NA Illumina [7723167] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266822 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-25003 levels in chronic kidney disease 4,784 European ancestry individuals NA Illumina [7723815] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266823 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-25091 levels in chronic kidney disease 3,779 European ancestry individuals NA Illumina [7723679] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266824 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-25105 levels in chronic kidney disease 4,043 European ancestry individuals NA Illumina [7724800] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266825 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24462 levels in chronic kidney disease 4,558 European ancestry individuals NA Illumina [7723006] (imputed) 2 X-24462 measurement http://www.ebi.ac.uk/efo/EFO_0800886 GCST90266726 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24462 levels in chronic kidney disease 4,898 European ancestry individuals NA Illumina [7724322] (imputed) 2 X-24462 measurement http://www.ebi.ac.uk/efo/EFO_0800886 GCST90266727 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24465 levels in chronic kidney disease 4,144 European ancestry individuals NA Illumina [7723557] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266728 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24466 levels in chronic kidney disease 4,031 European ancestry individuals NA Illumina [7722514] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266729 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24468 levels in chronic kidney disease 4,779 European ancestry individuals NA Illumina [7723613] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266730 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24469 levels in chronic kidney disease 4,524 European ancestry individuals NA Illumina [7723601] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266731 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24470 levels in chronic kidney disease 4,319 European ancestry individuals NA Illumina [7722891] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266732 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24473 levels in chronic kidney disease 4,856 European ancestry individuals NA Illumina [7723966] (imputed) 0 X-24473 measurement http://www.ebi.ac.uk/efo/EFO_0800887 GCST90266733 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24473 levels in chronic kidney disease 4,757 European ancestry individuals NA Illumina [7723435] (imputed) 0 X-24473 measurement http://www.ebi.ac.uk/efo/EFO_0800887 GCST90266734 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24474 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723758] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266735 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24474 levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723578] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266736 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24475 levels in chronic kidney disease 4,765 European ancestry individuals NA Illumina [7722713] (imputed) 0 X-24475 measurement http://www.ebi.ac.uk/efo/EFO_0800888 GCST90266737 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24475 levels in chronic kidney disease 3,688 European ancestry individuals NA Illumina [7722178] (imputed) 0 X-24475 measurement http://www.ebi.ac.uk/efo/EFO_0800888 GCST90266738 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24489 levels in chronic kidney disease 3,397 European ancestry individuals NA Illumina [7724336] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266739 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24493 levels in chronic kidney disease 3,088 European ancestry individuals NA Illumina [7723564] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266740 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24494 levels in chronic kidney disease 3,744 European ancestry individuals NA Illumina [7722703] (imputed) 2 X-24494 measurement http://www.ebi.ac.uk/efo/EFO_0800889 GCST90266741 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24494 levels in chronic kidney disease 4,880 European ancestry individuals NA Illumina [7723966] (imputed) 1 X-24494 measurement http://www.ebi.ac.uk/efo/EFO_0800889 GCST90266742 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24495 levels in chronic kidney disease 4,112 European ancestry individuals NA Illumina [7723016] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266743 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24499 levels in chronic kidney disease 4,673 European ancestry individuals NA Illumina [7723846] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266744 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24515 levels in chronic kidney disease 4,724 European ancestry individuals NA Illumina [7723706] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266745 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24518 levels in chronic kidney disease 4,355 European ancestry individuals NA Illumina [7723744] (imputed) 2 X-24518 measurement http://www.ebi.ac.uk/efo/EFO_0800890 GCST90266746 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24518 levels in chronic kidney disease 4,817 European ancestry individuals NA Illumina [7723088] (imputed) 2 X-24518 measurement http://www.ebi.ac.uk/efo/EFO_0800890 GCST90266747 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24519 levels in chronic kidney disease 4,853 European ancestry individuals NA Illumina [7723560] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266748 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24520 levels in chronic kidney disease 3,420 European ancestry individuals NA Illumina [7721910] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266749 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24522 levels in chronic kidney disease 1,741 European ancestry individuals NA Illumina [7726477] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266750 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25805 levels in chronic kidney disease 888 European ancestry individuals NA Illumina [7727273] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266851 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25806 levels in chronic kidney disease 2,532 European ancestry individuals NA Illumina [7722648] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266852 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25810 levels in chronic kidney disease 4,705 European ancestry individuals NA Illumina [7723575] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266853 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25828 levels in chronic kidney disease 4,927 European ancestry individuals NA Illumina [7724246] (imputed) 0 X-25828 measurement http://www.ebi.ac.uk/efo/EFO_0800936 GCST90266854 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25982 levels in chronic kidney disease 4,655 European ancestry individuals NA Illumina [7723651] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266855 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-25983 levels in chronic kidney disease 4,880 European ancestry individuals NA Illumina [7724107] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266856 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-26008 levels in chronic kidney disease 4,222 European ancestry individuals NA Illumina [7724113] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266857 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-26054 levels in chronic kidney disease 3,829 European ancestry individuals NA Illumina [7723559] (imputed) 2 X-26054 measurement http://www.ebi.ac.uk/efo/EFO_0800939 GCST90266858 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-26058 levels in chronic kidney disease 4,856 European ancestry individuals NA Illumina [7723674] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266859 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-26062 levels in chronic kidney disease 2,123 European ancestry individuals NA Illumina [7720701] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266860 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-26109 levels in chronic kidney disease 3,565 European ancestry individuals NA Illumina [7722803] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266861 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-26111 levels in chronic kidney disease 4,569 European ancestry individuals NA Illumina [7723169] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266862 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-26119 levels in chronic kidney disease 4,175 European ancestry individuals NA Illumina [7723742] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266863 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma xanthine levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90266864 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine xanthine levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724629] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90266865 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine xanthopterin levels in chronic kidney disease 4,780 European ancestry individuals NA Illumina [7723839] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266866 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine xanthosine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723559] (imputed) 0 xanthosine measurement http://www.ebi.ac.uk/efo/EFO_0010549 GCST90266867 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma xanthurenate levels in chronic kidney disease 4,741 European ancestry individuals NA Illumina [7724279] (imputed) 2 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90266868 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine xanthurenate levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724687] (imputed) 1 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90266869 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma ximenoylcarnitine (C26:1)* levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7724281] (imputed) 4 ximenoylcarnitine (C26:1) measurement http://www.ebi.ac.uk/efo/EFO_0800543 GCST90266870 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma xylose levels in chronic kidney disease 3,447 European ancestry individuals NA Illumina [7723396] (imputed) 0 xylose measurement http://www.ebi.ac.uk/efo/EFO_0800153 GCST90266871 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine xylose levels in chronic kidney disease 4,442 European ancestry individuals NA Illumina [7724947] (imputed) 0 xylose measurement http://www.ebi.ac.uk/efo/EFO_0800153 GCST90266872 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24528 levels in chronic kidney disease 4,899 European ancestry individuals NA Illumina [7724651] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266751 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24530 levels in chronic kidney disease 3,697 European ancestry individuals NA Illumina [7723133] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266752 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24531 levels in chronic kidney disease 3,996 European ancestry individuals NA Illumina [7724811] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266753 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24541 levels in chronic kidney disease 1,663 European ancestry individuals NA Illumina [7722404] (imputed) 0 X-24541 measurement http://www.ebi.ac.uk/efo/EFO_0800891 GCST90266754 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24541 levels in chronic kidney disease 2,344 European ancestry individuals NA Illumina [7726358] (imputed) 0 X-24541 measurement http://www.ebi.ac.uk/efo/EFO_0800891 GCST90266755 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24543 levels in chronic kidney disease 4,635 European ancestry individuals NA Illumina [7723738] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266756 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24544 levels in chronic kidney disease 4,363 European ancestry individuals NA Illumina [7723465] (imputed) 1 X-24544 measurement http://www.ebi.ac.uk/efo/EFO_0800892 GCST90266757 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24544 levels in chronic kidney disease 1,610 European ancestry individuals NA Illumina [7724533] (imputed) 0 X-24544 measurement http://www.ebi.ac.uk/efo/EFO_0800892 GCST90266758 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24545 levels in chronic kidney disease 2,982 European ancestry individuals NA Illumina [7722745] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266759 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24546 levels in chronic kidney disease 2,779 European ancestry individuals NA Illumina [7724484] (imputed) 1 X-24546 measurement http://www.ebi.ac.uk/efo/EFO_0800893 GCST90266760 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24546 levels in chronic kidney disease 4,109 European ancestry individuals NA Illumina [7723743] (imputed) 2 X-24546 measurement http://www.ebi.ac.uk/efo/EFO_0800893 GCST90266761 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24549 levels in chronic kidney disease 2,842 European ancestry individuals NA Illumina [7724246] (imputed) 0 X-24549 measurement http://www.ebi.ac.uk/efo/EFO_0800894 GCST90266762 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24549 levels in chronic kidney disease 4,356 European ancestry individuals NA Illumina [7723834] (imputed) 0 X-24549 measurement http://www.ebi.ac.uk/efo/EFO_0800894 GCST90266763 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24556 levels in chronic kidney disease 4,884 European ancestry individuals NA Illumina [7723816] (imputed) 1 X-24556 measurement http://www.ebi.ac.uk/efo/EFO_0800895 GCST90266764 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24556 levels in chronic kidney disease 4,886 European ancestry individuals NA Illumina [7724487] (imputed) 1 X-24556 measurement http://www.ebi.ac.uk/efo/EFO_0800895 GCST90266765 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24571 levels in chronic kidney disease 3,086 European ancestry individuals NA Illumina [7722836] (imputed) 0 X-24571 measurement http://www.ebi.ac.uk/efo/EFO_0800896 GCST90266766 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24571 levels in chronic kidney disease 3,311 European ancestry individuals NA Illumina [7723417] (imputed) 0 X-24571 measurement http://www.ebi.ac.uk/efo/EFO_0800896 GCST90266767 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24583 levels in chronic kidney disease 4,870 European ancestry individuals NA Illumina [7723812] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266768 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24585 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266769 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24586 levels in chronic kidney disease 4,898 European ancestry individuals NA Illumina [7724401] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266770 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24587 levels in chronic kidney disease 4,869 European ancestry individuals NA Illumina [7724120] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266771 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24588 levels in chronic kidney disease 4,869 European ancestry individuals NA Illumina [7723570] (imputed) 3 X-24588 measurement http://www.ebi.ac.uk/efo/EFO_0800898 GCST90266772 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24588 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723569] (imputed) 2 X-24588 measurement http://www.ebi.ac.uk/efo/EFO_0800898 GCST90266773 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24590 levels in chronic kidney disease 4,836 European ancestry individuals NA Illumina [7723878] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266774 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24623 levels in chronic kidney disease 1,930 European ancestry individuals NA Illumina [7724775] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266775 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24625 levels in chronic kidney disease 4,071 European ancestry individuals NA Illumina [7723874] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266776 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24637 levels in chronic kidney disease 403 European ancestry individuals NA Illumina [7707438] (imputed) 0 X-24637 measurement http://www.ebi.ac.uk/efo/EFO_0800899 GCST90266777 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24657 levels in chronic kidney disease 2,977 European ancestry individuals NA Illumina [7724503] (imputed) 0 X-24657 measurement http://www.ebi.ac.uk/efo/EFO_0800900 GCST90266778 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24660 levels in chronic kidney disease 2,393 European ancestry individuals NA Illumina [7724289] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266779 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24669 levels in chronic kidney disease 1,329 European ancestry individuals NA Illumina [7726527] (imputed) 0 X-24669 measurement http://www.ebi.ac.uk/efo/EFO_0800901 GCST90266780 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24680 levels in chronic kidney disease 4,798 European ancestry individuals NA Illumina [7724056] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266781 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24686 levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723575] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266782 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24728 levels in chronic kidney disease 4,503 European ancestry individuals NA Illumina [7723342] (imputed) 0 X-24728 measurement http://www.ebi.ac.uk/efo/EFO_0800903 GCST90266783 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24736 levels in chronic kidney disease 3,112 European ancestry individuals NA Illumina [7722900] (imputed) 1 X-24736 measurement http://www.ebi.ac.uk/efo/EFO_0800904 GCST90266784 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24736 levels in chronic kidney disease 2,255 European ancestry individuals NA Illumina [7724084] (imputed) 1 X-24736 measurement http://www.ebi.ac.uk/efo/EFO_0800904 GCST90266785 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24757 levels in chronic kidney disease 3,708 European ancestry individuals NA Illumina [7722130] (imputed) 0 X-24757 measurement http://www.ebi.ac.uk/efo/EFO_0800905 GCST90266786 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24757 levels in chronic kidney disease 4,900 European ancestry individuals NA Illumina [7723848] (imputed) 0 X-24757 measurement http://www.ebi.ac.uk/efo/EFO_0800905 GCST90266787 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24761 levels in chronic kidney disease 3,372 European ancestry individuals NA Illumina [7722245] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266788 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24762 levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724237] (imputed) 0 X-24762 measurement http://www.ebi.ac.uk/efo/EFO_0800906 GCST90266789 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24763 levels in chronic kidney disease 4,512 European ancestry individuals NA Illumina [7722976] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266790 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24763 levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723615] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266791 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24764 levels in chronic kidney disease 3,431 European ancestry individuals NA Illumina [7723230] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266792 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24764 levels in chronic kidney disease 4,865 European ancestry individuals NA Illumina [7723440] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266793 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24765 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266794 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24767 levels in chronic kidney disease 4,315 European ancestry individuals NA Illumina [7723703] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266795 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24768 levels in chronic kidney disease 4,410 European ancestry individuals NA Illumina [7723150] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266796 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24794 levels in chronic kidney disease 4,210 European ancestry individuals NA Illumina [7722578] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266797 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-24795 levels in chronic kidney disease 3,074 European ancestry individuals NA Illumina [7721647] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266798 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24795 levels in chronic kidney disease 4,807 European ancestry individuals NA Illumina [7723646] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266799 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-24796 levels in chronic kidney disease 4,776 European ancestry individuals NA Illumina [7723426] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266800 Genome-wide genotyping array 2023-06-19 36757925 Jiang X 2023-02-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36757925 GWAS on retinal vasculometry phenotypes. Retinal arteriolar tortuosity 52,798 European ancestry individuals 4,987 European ancestry individuals NR [19368057] (imputed) 98 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90270397 Genome-wide genotyping array 2023-06-19 36757925 Jiang X 2023-02-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36757925 GWAS on retinal vasculometry phenotypes. Retinal arteriolar width 52,798 European ancestry individuals 4,987 European ancestry individuals NR [19368057] (imputed) 3 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90270398 Genome-wide genotyping array 2023-06-19 36757925 Jiang X 2023-02-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36757925 GWAS on retinal vasculometry phenotypes. Retinal venular tortuosity 52,798 European ancestry individuals 4,987 European ancestry individuals NR [19368057] (imputed) 23 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90270399 Genome-wide genotyping array 2023-06-19 36757925 Jiang X 2023-02-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36757925 GWAS on retinal vasculometry phenotypes. Retinal venular width 52,798 European ancestry individuals 4,987 European ancestry individuals NR [19368057] (imputed) 20 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90270400 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine taurocyamine levels in chronic kidney disease 1,214 European ancestry individuals NA Illumina [7721280] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266042 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurodeoxycholate levels in chronic kidney disease 4,127 European ancestry individuals NA Illumina [7723273] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90266043 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurodeoxycholic acid 3-sulfate levels in chronic kidney disease 3,356 European ancestry individuals NA Illumina [7721665] (imputed) 1 taurodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800386 GCST90266044 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine taurodeoxycholic acid 3-sulfate levels in chronic kidney disease 3,905 European ancestry individuals NA Illumina [7722933] (imputed) 1 taurodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800386 GCST90266045 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurolithocholate 3-sulfate levels in chronic kidney disease 4,724 European ancestry individuals NA Illumina [7724057] (imputed) 0 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90266046 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine taurolithocholate 3-sulfate levels in chronic kidney disease 4,566 European ancestry individuals NA Illumina [7724104] (imputed) 0 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90266047 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tauroursodeoxycholate levels in chronic kidney disease 1,805 European ancestry individuals NA Illumina [7722766] (imputed) 0 tauroursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800327 GCST90266048 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma testosterone sulfate levels in chronic kidney disease 597 European ancestry individuals NA Illumina [7735289] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90266049 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tetradecadienedioate (C14:2-DC)* levels in chronic kidney disease 4,382 European ancestry individuals NA Illumina [7722558] (imputed) 2 tetradecadienedioate (C14:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800585 GCST90266050 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tetradecadienoate (14:2)* levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723781] (imputed) 0 tetradecadienoate (14:2) measurement http://www.ebi.ac.uk/efo/EFO_0800570 GCST90266051 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tetradecanedioate (C14-DC) levels in chronic kidney disease 4,944 European ancestry individuals NA Illumina [7724617] (imputed) 1 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90266052 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tetrahydrocorticosterone glucuronide (3) levels in chronic kidney disease 4,852 European ancestry individuals NA Illumina [7723879] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266053 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tetrahydrocortisol glucuronide levels in chronic kidney disease 4,788 European ancestry individuals NA Illumina [7724221] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266054 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tetrahydrocortisol sulfate (1) levels in chronic kidney disease 1,715 European ancestry individuals NA Illumina [7721339] (imputed) 0 tetrahydrocortisol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800582 GCST90266055 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tetrahydrocortisone glucuronide (5) levels in chronic kidney disease 4,526 European ancestry individuals NA Illumina [7723915] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266056 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tetrahydrocortisone glucuronide (5) levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723692] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266057 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tetrahydrocortisone levels in chronic kidney disease 2,849 European ancestry individuals NA Illumina [7723009] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266058 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma theanine levels in chronic kidney disease 1,276 European ancestry individuals NA Illumina [7729202] (imputed) 0 theanine measurement http://www.ebi.ac.uk/efo/EFO_0800943 GCST90266059 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine theanine levels in chronic kidney disease 1,787 European ancestry individuals NA Illumina [7727487] (imputed) 0 theanine measurement http://www.ebi.ac.uk/efo/EFO_0800943 GCST90266060 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma theobromine levels in chronic kidney disease 4,927 European ancestry individuals NA Illumina [7724518] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90266061 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine theobromine levels in chronic kidney disease 4,883 European ancestry individuals NA Illumina [7724274] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90266062 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma theophylline levels in chronic kidney disease 4,816 European ancestry individuals NA Illumina [7723893] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90266063 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma malate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90265466 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine malate levels in chronic kidney disease 4,864 European ancestry individuals NA Illumina [7724075] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90265467 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma maleate levels in chronic kidney disease 4,927 European ancestry individuals NA Illumina [7724024] (imputed) 0 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90265468 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265967 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265968 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/22:2, d18:2/22:1, d16:1/24:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265969 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/24:1, d18:2/24:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 Sphingomyelin (d18:1/24:1, d18:2/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0022113 GCST90265970 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0)* levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724398] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265971 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/14:0, d18:1/14:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 Sphingomyelin (d18:2/14:0, d18:1/14:1) measurement http://www.ebi.ac.uk/efo/EFO_0022114 GCST90265972 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/16:0, d18:1/16:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 Sphingomyelin (d18:2/16:0, d18:1/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0022115 GCST90265973 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/18:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265974 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/21:0, d16:2/23:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265975 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022116 GCST90265976 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/23:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265977 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/24:1, d18:1/24:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723859] (imputed) 0 Sphingomyelin (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0022117 GCST90265978 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:2/24:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265979 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingosine 1-phosphate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90265980 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingosine levels in chronic kidney disease 4,766 European ancestry individuals NA Illumina [7723486] (imputed) 0 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90265981 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma stachydrine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90265982 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine stachydrine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723572] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90265983 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma stearate (18:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90265984 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma stearidonate (18:4n3) levels in chronic kidney disease 4,842 European ancestry individuals NA Illumina [7724594] (imputed) 1 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90265985 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma stearoyl sphingomyelin (d18:1/18:0) levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723850] (imputed) 1 stearoyl sphingomyelin (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800611 GCST90265986 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma stearoyl-arachidonoyl-glycerol (18:0/20:4) [1]* levels in chronic kidney disease 2,062 European ancestry individuals NA Illumina [7722649] (imputed) 1 stearoyl-arachidonoyl-glycerol (18:0/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800511 GCST90265987 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma stearoylcarnitine (C18) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90265988 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma stearoylcholine* levels in chronic kidney disease 4,721 European ancestry individuals NA Illumina [7723188] (imputed) 0 stearoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800534 GCST90265989 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma suberate (C8-DC) levels in chronic kidney disease 3,839 European ancestry individuals NA Illumina [7724122] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90265990 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine suberate (C8-DC) levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723551] (imputed) 1 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90265991 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S-1-pyrroline-5-carboxylate levels in chronic kidney disease 4,179 European ancestry individuals NA Illumina [7724761] (imputed) 0 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90265917 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-adenosylhomocysteine (SAH) levels in chronic kidney disease 3,629 European ancestry individuals NA Illumina [7722369] (imputed) 1 S-adenosylhomocysteine measurement http://www.ebi.ac.uk/efo/EFO_0010531 GCST90265918 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S-adenosylhomocysteine (SAH) levels in chronic kidney disease 4,789 European ancestry individuals NA Illumina [7724561] (imputed) 1 S-adenosylhomocysteine measurement http://www.ebi.ac.uk/efo/EFO_0010531 GCST90265919 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S-adenosylmethionine (SAM) levels in chronic kidney disease 4,483 European ancestry individuals NA Illumina [7725449] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265920 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-allylcysteine levels in chronic kidney disease 2,758 European ancestry individuals NA Illumina [7722178] (imputed) 0 S-allylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800985 GCST90265921 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-carboxyethylcysteine levels in chronic kidney disease 4,947 European ancestry individuals NA Illumina [7724719] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265922 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S-carboxymethyl-L-cysteine levels in chronic kidney disease 4,392 European ancestry individuals NA Illumina [7723586] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265923 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-methylcysteine levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723657] (imputed) 1 S-methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800054 GCST90265924 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-methylcysteine sulfoxide levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 S-methylcysteine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0800058 GCST90265925 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S-methylcysteine sulfoxide levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 S-methylcysteine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0800058 GCST90265926 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma S-methylmethionine levels in chronic kidney disease 3,418 European ancestry individuals NA Illumina [7723101] (imputed) 0 S-methylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800042 GCST90265927 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S-methylmethionine levels in chronic kidney disease 891 European ancestry individuals NA Illumina [7731278] (imputed) 0 S-methylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800042 GCST90265928 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine S(2-carboxyethyl)mercapturic acid levels in chronic kidney disease 3,647 European ancestry individuals NA Illumina [7723260] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265929 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma saccharin levels in chronic kidney disease 3,646 European ancestry individuals NA Illumina [7725174] (imputed) 0 saccharin measurement http://www.ebi.ac.uk/efo/EFO_0021168 GCST90265930 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine saccharin levels in chronic kidney disease 4,746 European ancestry individuals NA Illumina [7724454] (imputed) 0 saccharin measurement http://www.ebi.ac.uk/efo/EFO_0021168 GCST90265931 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine saccharopine levels in chronic kidney disease 4,216 European ancestry individuals NA Illumina [7722743] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265932 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma salicylate levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723706] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90265933 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine salicylate levels in chronic kidney disease 4,587 European ancestry individuals NA Illumina [7724057] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90265934 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma salicyluric glucuronide* levels in chronic kidney disease 3,154 European ancestry individuals NA Illumina [7721373] (imputed) 0 salicyluric glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0021162 GCST90265935 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine salicyluric glucuronide* levels in chronic kidney disease 4,846 European ancestry individuals NA Illumina [7724968] (imputed) 0 salicyluric glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0021162 GCST90265936 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sarcosine levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7723851] (imputed) 1 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90265937 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sarcosine levels in chronic kidney disease 4,223 European ancestry individuals NA Illumina [7724388] (imputed) 0 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90265938 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine scyllo-inositol levels in chronic kidney disease 1,457 European ancestry individuals NA Illumina [7720120] (imputed) 0 scyllo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0011001 GCST90265939 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sebacate (C10-DC) levels in chronic kidney disease 4,731 European ancestry individuals NA Illumina [7723506] (imputed) 0 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90265940 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sebacate (C10-DC) levels in chronic kidney disease 3,850 European ancestry individuals NA Illumina [7724336] (imputed) 1 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90265941 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine maleate levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723724] (imputed) 0 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90265469 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine malonate levels in chronic kidney disease 4,466 European ancestry individuals NA Illumina [7723070] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265470 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma malonylcarnitine levels in chronic kidney disease 4,869 European ancestry individuals NA Illumina [7723760] (imputed) 0 malonylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800232 GCST90265471 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine malonylcarnitine levels in chronic kidney disease 4,644 European ancestry individuals NA Illumina [7724592] (imputed) 0 malonylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800232 GCST90265472 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine maltitol/lactitol/cellobiotol/palatinol levels in chronic kidney disease 3,364 European ancestry individuals NA Illumina [7721795] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265473 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma maltol sulfate levels in chronic kidney disease 4,029 European ancestry individuals NA Illumina [7723373] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265474 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine maltol sulfate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723547] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265475 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine mandelate levels in chronic kidney disease 404 European ancestry individuals NA Illumina [7707293] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265476 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma mannitol/sorbitol levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723786] (imputed) 0 mannitol measurement, sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0021027, http://www.ebi.ac.uk/efo/EFO_0010533 GCST90265477 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine mannitol/sorbitol levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723658] (imputed) 0 mannitol measurement, sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0021027, http://www.ebi.ac.uk/efo/EFO_0010533 GCST90265478 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma mannonate* levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7724001] (imputed) 1 mannonate measurement http://www.ebi.ac.uk/efo/EFO_0800971 GCST90265479 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine mannonate* levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723551] (imputed) 0 mannonate measurement http://www.ebi.ac.uk/efo/EFO_0800971 GCST90265480 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma mannose levels in chronic kidney disease 4,946 European ancestry individuals NA Illumina [7724559] (imputed) 1 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90265481 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine mannose levels in chronic kidney disease 3,018 European ancestry individuals NA Illumina [7724145] (imputed) 1 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90265482 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma margaramide (17:0)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265483 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma margarate (17:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90265484 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma margaroylcarnitine (C17)* levels in chronic kidney disease 4,768 European ancestry individuals NA Illumina [7724047] (imputed) 0 margaroylcarnitine (C17) measurement http://www.ebi.ac.uk/efo/EFO_0800345 GCST90265485 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma mead acid (20:3n9) levels in chronic kidney disease 2,945 European ancestry individuals NA Illumina [7723582] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265486 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine mesaconate (methylfumarate) levels in chronic kidney disease 4,824 European ancestry individuals NA Illumina [7723817] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265487 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma metabolonic lactone sulfate levels in chronic kidney disease 4,811 European ancestry individuals NA Illumina [7723282] (imputed) 3 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90265488 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma metformin levels in chronic kidney disease 719 European ancestry individuals NA Illumina [7726094] (imputed) 0 metformin measurement http://www.ebi.ac.uk/efo/EFO_0801177 GCST90265489 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine metformin levels in chronic kidney disease 1,883 European ancestry individuals NA Illumina [7726057] (imputed) 0 metformin measurement http://www.ebi.ac.uk/efo/EFO_0801177 GCST90265490 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methionine levels in chronic kidney disease 4,945 European ancestry individuals NA Illumina [7724598] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90265491 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma methionine sulfone levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90265492 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine methionine sulfone levels in chronic kidney disease 4,888 European ancestry individuals NA Illumina [7724548] (imputed) 2 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90265493 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma suberoylcarnitine (C8-DC) levels in chronic kidney disease 4,861 European ancestry individuals NA Illumina [7723621] (imputed) 3 suberoylcarnitine (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800382 GCST90265992 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine suberoylcarnitine (C8-DC) levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723533] (imputed) 3 suberoylcarnitine (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800382 GCST90265993 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma succinate levels in chronic kidney disease 4,945 European ancestry individuals NA Illumina [7724706] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90265994 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine succinate levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723832] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90265995 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine succinimide levels in chronic kidney disease 4,089 European ancestry individuals NA Illumina [7724863] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265996 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma succinoyltaurine levels in chronic kidney disease 4,746 European ancestry individuals NA Illumina [7724567] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265997 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma succinylcarnitine (C4-DC) levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723919] (imputed) 3 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90265998 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine succinylcarnitine (C4-DC) levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90265999 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine succinylglutamine levels in chronic kidney disease 4,707 European ancestry individuals NA Illumina [7722936] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266000 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sucrose levels in chronic kidney disease 4,572 European ancestry individuals NA Illumina [7723542] (imputed) 0 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90266001 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sucrose levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723695] (imputed) 0 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90266002 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C15H17NO3 (1)* levels in chronic kidney disease 4,659 European ancestry individuals NA Illumina [7722697] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266003 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C15H17NO3 (2)* levels in chronic kidney disease 4,736 European ancestry individuals NA Illumina [7723390] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266004 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H17NO3 (1)* levels in chronic kidney disease 4,472 European ancestry individuals NA Illumina [7724630] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266005 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H17NO3 (2)* levels in chronic kidney disease 2,290 European ancestry individuals NA Illumina [7724553] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266006 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H19NO3 (1)* levels in chronic kidney disease 4,514 European ancestry individuals NA Illumina [7723180] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266007 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sulfate of piperine metabolite C16H19NO3 (2)* levels in chronic kidney disease 4,852 European ancestry individuals NA Illumina [7723547] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90266008 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H19NO3 (2)* levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723957] (imputed) 1 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90266009 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sulfate of piperine metabolite C16H19NO3 (3)* levels in chronic kidney disease 4,706 European ancestry individuals NA Illumina [7723275] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90266010 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H19NO3 (3)* levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723974] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90266011 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H19NO4 (1)* levels in chronic kidney disease 3,959 European ancestry individuals NA Illumina [7721807] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266012 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H19NO4 (2)* levels in chronic kidney disease 4,786 European ancestry individuals NA Illumina [7724403] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266013 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H19NO4 (3)* levels in chronic kidney disease 4,801 European ancestry individuals NA Illumina [7723741] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266014 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C16H19NO4 (4)* levels in chronic kidney disease 4,882 European ancestry individuals NA Illumina [7724220] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266015 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sulfate of piperine metabolite C18H21NO3 (1)* levels in chronic kidney disease 4,307 European ancestry individuals NA Illumina [7722680] (imputed) 2 sulfate of piperine metabolite C18H21NO3 (1) measurement http://www.ebi.ac.uk/efo/EFO_0801036 GCST90266016 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C18H21NO3 (1)* levels in chronic kidney disease 4,764 European ancestry individuals NA Illumina [7723528] (imputed) 2 sulfate of piperine metabolite C18H21NO3 (1) measurement http://www.ebi.ac.uk/efo/EFO_0801036 GCST90266017 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C18H21NO3 (2)* levels in chronic kidney disease 4,326 European ancestry individuals NA Illumina [7724068] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266018 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sulfate of piperine metabolite C18H21NO3 (3)* levels in chronic kidney disease 4,250 European ancestry individuals NA Illumina [7723430] (imputed) 1 sulfate of piperine metabolite C18H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801037 GCST90266019 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate of piperine metabolite C18H21NO3 (3)* levels in chronic kidney disease 4,868 European ancestry individuals NA Illumina [7723866] (imputed) 2 sulfate of piperine metabolite C18H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801037 GCST90266020 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sulfate* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90266021 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulfate* levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90266022 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulforaphane levels in chronic kidney disease 369 European ancestry individuals NA Illumina [7719570] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266023 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulforaphane-cysteine levels in chronic kidney disease 1,389 European ancestry individuals NA Illumina [7727779] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266024 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sulforaphane-N-acetyl-cysteine levels in chronic kidney disease 899 European ancestry individuals NA Illumina [7731253] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266025 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma syringol sulfate levels in chronic kidney disease 2,295 European ancestry individuals NA Illumina [7725441] (imputed) 0 syringol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801003 GCST90266026 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine syringol sulfate levels in chronic kidney disease 4,825 European ancestry individuals NA Illumina [7723326] (imputed) 0 syringol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801003 GCST90266027 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tartarate levels in chronic kidney disease 4,839 European ancestry individuals NA Illumina [7724768] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90266028 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tartarate levels in chronic kidney disease 4,555 European ancestry individuals NA Illumina [7723664] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90266029 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tartronate (hydroxymalonate) levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723752] (imputed) 0 tartronate (hydroxymalonate) measurement http://www.ebi.ac.uk/efo/EFO_0800944 GCST90266030 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90266031 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine taurine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90266032 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma tauro-beta-muricholate levels in chronic kidney disease 1,538 European ancestry individuals NA Illumina [7723867] (imputed) 1 tauro-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800213 GCST90266033 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine tauro-beta-muricholate levels in chronic kidney disease 1,507 European ancestry individuals NA Illumina [7719922] (imputed) 1 tauro-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800213 GCST90266034 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurochenodeoxycholate levels in chronic kidney disease 4,944 European ancestry individuals NA Illumina [7724658] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90266035 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurochenodeoxycholic acid 3-sulfate levels in chronic kidney disease 3,596 European ancestry individuals NA Illumina [7723683] (imputed) 0 taurochenodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800584 GCST90266036 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine taurochenodeoxycholic acid 3-sulfate levels in chronic kidney disease 3,519 European ancestry individuals NA Illumina [7722605] (imputed) 0 taurochenodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800584 GCST90266037 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurocholate levels in chronic kidney disease 4,603 European ancestry individuals NA Illumina [7723244] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90266038 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine taurocholate levels in chronic kidney disease 365 European ancestry individuals NA Illumina [7716581] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90266039 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma taurocholenate sulfate* levels in chronic kidney disease 4,937 European ancestry individuals NA Illumina [7724600] (imputed) 1 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90266040 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine taurocholenate sulfate* levels in chronic kidney disease 4,657 European ancestry individuals NA Illumina [7723922] (imputed) 1 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90266041 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sedoheptulose levels in chronic kidney disease 401 European ancestry individuals NA Illumina [7711864] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265942 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma serine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90265943 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine serine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90265944 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma serotonin levels in chronic kidney disease 2,420 European ancestry individuals NA Illumina [7723905] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90265945 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine serotonin levels in chronic kidney disease 3,887 European ancestry individuals NA Illumina [7724715] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90265946 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine shikimate levels in chronic kidney disease 4,511 European ancestry individuals NA Illumina [7723937] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265947 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine sinapate levels in chronic kidney disease 670 European ancestry individuals NA Illumina [7719381] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265948 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma solanidine levels in chronic kidney disease 1,487 European ancestry individuals NA Illumina [7726539] (imputed) 1 solanidine measurement http://www.ebi.ac.uk/efo/EFO_0800966 GCST90265949 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma spermidine levels in chronic kidney disease 3,555 European ancestry individuals NA Illumina [7722850] (imputed) 0 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90265950 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine spermidine levels in chronic kidney disease 2,881 European ancestry individuals NA Illumina [7725136] (imputed) 0 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90265951 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine spermine levels in chronic kidney disease 948 European ancestry individuals NA Illumina [7734474] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265952 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingadienine levels in chronic kidney disease 3,368 European ancestry individuals NA Illumina [7723360] (imputed) 0 sphingadienine measurement http://www.ebi.ac.uk/efo/EFO_0800526 GCST90265953 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphinganine-1-phosphate levels in chronic kidney disease 4,369 European ancestry individuals NA Illumina [7723124] (imputed) 0 sphinganine-1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800274 GCST90265954 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d17:1/14:0, d16:1/15:0)* levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723854] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265955 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d17:1/16:0, d18:1/15:0, d16:1/17:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265956 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d17:2/16:0, d18:2/15:0)* levels in chronic kidney disease 4,950 European ancestry individuals NA Illumina [7724239] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265957 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:0/18:0, d19:0/17:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265958 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:0/20:0, d16:0/22:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265959 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/14:0, d16:1/16:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265960 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265961 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/18:1, d18:2/18:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265962 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/19:0, d19:1/18:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265963 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/20:0, d16:1/22:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265964 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/20:1, d18:2/20:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265965 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma sphingomyelin (d18:1/20:2, d18:2/20:1, d16:1/22:2)* levels in chronic kidney disease 4,935 European ancestry individuals NA Illumina [7724713] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90265966 Genome-wide genotyping array 2023-05-15 35348614 Strippel C 2022-03-28 Brain www.ncbi.nlm.nih.gov/pubmed/35348614 A genome-wide association study in autoimmune neurological syndromes with anti-GAD65 autoantibodies. Autoimmune neurological syndromes with anti-GAD65 autoantibodies 167 German ancestry cases, 1,047 German ancestry controls NA Illumina [7012247] (imputed) 35 anti-GAD65 autoimmune neurological syndromes http://www.ebi.ac.uk/efo/EFO_0803379 GCST90257012 Genome-wide genotyping array 2022-05-12 35039640 Shelton JF 2022-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35039640 The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste. COVID-19 symptoms (loss of smell or taste vs no loss of smell or taste) 33,336 European ancestry cases, 16,257 European ancestry controls NA Illumina [NR] (imputed) 0 Abnormality of the sense of smell, COVID-19 symptoms measurement, ageusia http://purl.obolibrary.org/obo/HP_0004408, http://www.ebi.ac.uk/efo/EFO_0600019, http://www.ebi.ac.uk/efo/EFO_1001758 GCST90102487 Genome-wide genotyping array 2022-05-12 35039640 Shelton JF 2022-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35039640 The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste. COVID-19 symptoms (loss of smell or taste vs no loss of smell or taste) 284 South Asian ancestry cases, 167 South Asian ancestry controls NA Illumina [NR] (imputed) 0 Abnormality of the sense of smell, COVID-19 symptoms measurement, ageusia http://purl.obolibrary.org/obo/HP_0004408, http://www.ebi.ac.uk/efo/EFO_0600019, http://www.ebi.ac.uk/efo/EFO_1001758 GCST90102488 Genome-wide genotyping array 2022-05-12 35039640 Shelton JF 2022-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35039640 The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste. COVID-19 symptoms (loss of smell or taste vs no loss of smell or taste) 1,860 African American cases, 949 African American controls NA Illumina [NR] (imputed) 0 Abnormality of the sense of smell, COVID-19 symptoms measurement, ageusia http://purl.obolibrary.org/obo/HP_0004408, http://www.ebi.ac.uk/efo/EFO_0600019, http://www.ebi.ac.uk/efo/EFO_1001758 GCST90102489 Genome-wide genotyping array 2022-05-12 35039640 Shelton JF 2022-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35039640 The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste. COVID-19 symptoms (loss of smell or taste vs no loss of smell or taste) 626 East Asian ancestry cases, 338 East Asian ancestry controls NA Illumina [NR] (imputed) 0 Abnormality of the sense of smell, COVID-19 symptoms measurement, ageusia http://purl.obolibrary.org/obo/HP_0004408, http://www.ebi.ac.uk/efo/EFO_0600019, http://www.ebi.ac.uk/efo/EFO_1001758 GCST90102490 Genome-wide genotyping array 2022-05-12 35039640 Shelton JF 2022-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35039640 The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste. COVID-19 symptoms (loss of smell or taste vs no loss of smell or taste) 9,233 Latino cases, 3,944 Latino controls NA Illumina [NR] (imputed) 0 Abnormality of the sense of smell, COVID-19 symptoms measurement, ageusia http://purl.obolibrary.org/obo/HP_0004408, http://www.ebi.ac.uk/efo/EFO_0600019, http://www.ebi.ac.uk/efo/EFO_1001758 GCST90102491 Genome-wide genotyping array 2022-05-12 35039640 Shelton JF 2022-01-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35039640 The UGT2A1/UGT2A2 locus is associated with COVID-19-related loss of smell or taste. COVID-19 symptoms (loss of smell or taste vs no loss of smell or taste) 33,336 European ancestry cases, 16,257 European ancestry controls, 9,233 Latino cases, 3,944 Latino controls, 1,860 African American cases, 949 African American controls, 626 East Asian ancestry cases, 338 East Asian ancestry controls, 284 South Asian ancestry cases, 167 South Asian ancestry controls, 1,959 cases, 888 controls NA Illumina [NR] (imputed) 2 Abnormality of the sense of smell, COVID-19 symptoms measurement, ageusia http://purl.obolibrary.org/obo/HP_0004408, http://www.ebi.ac.uk/efo/EFO_0600019, http://www.ebi.ac.uk/efo/EFO_1001758 GCST90102492 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dimethyl sulfone levels in chronic kidney disease 4,165 European ancestry individuals NA Illumina [7724476] (imputed) 0 dimethyl sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800979 GCST90265041 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dimethylarginine (SDMA + ADMA) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90265042 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma (14 or 15)-methylpalmitate (a17:0 or i17:0) levels in chronic kidney disease 4,929 European ancestry individuals NA Illumina [7724099] (imputed) 0 (14 or 15)-methylpalmitate (a17:0 or i17:0) measurement http://www.ebi.ac.uk/efo/EFO_0800329 GCST90264176 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma (16 or 17)-methylstearate (a19:0 or i19:0) levels in chronic kidney disease 4,948 European ancestry individuals NA Illumina [7724693] (imputed) 0 (16 or 17)-methylstearate (a19:0 or i19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800313 GCST90264177 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma (2 or 3)-decenoate (10:1n7 or n8) levels in chronic kidney disease 4,354 European ancestry individuals NA Illumina [7722819] (imputed) 0 (2 or 3)-decenoate (10:1n7 or n8) measurement http://www.ebi.ac.uk/efo/EFO_0800594 GCST90264178 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine (2-butoxyethoxy)acetic acid (formerly X - 23667) levels in chronic kidney disease 4,311 European ancestry individuals NA Illumina [7723729] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264179 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine (2-butoxyethoxy)acetic acid (formerly X - 24759) levels in chronic kidney disease 4,808 European ancestry individuals NA Illumina [7723272] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264180 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma (2-butoxyethoxy)acetic acid levels in chronic kidney disease 2,709 European ancestry individuals NA Illumina [7723061] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264181 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma (2,4 or 2,5)-dimethylphenol sulfate levels in chronic kidney disease 4,092 European ancestry individuals NA Illumina [7721478] (imputed) 0 (2,4 or 2,5)-dimethylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801039 GCST90264182 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine (2,4 or 2,5)-dimethylphenol sulfate levels in chronic kidney disease 4,850 European ancestry individuals NA Illumina [7724022] (imputed) 0 (2,4 or 2,5)-dimethylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801039 GCST90264183 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine (N(1) + N(8))-acetylspermidine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 4 (N(1) + N(8))-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0800091 GCST90264184 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma (R)-3-hydroxybutyrylcarnitine levels in chronic kidney disease 4,524 European ancestry individuals NA Illumina [7722534] (imputed) 0 (R)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800344 GCST90264185 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine (R)-3-hydroxybutyrylcarnitine levels in chronic kidney disease 3,279 European ancestry individuals NA Illumina [7722416] (imputed) 0 (R)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800344 GCST90264186 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma (S)-3-hydroxybutyrylcarnitine levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723746] (imputed) 0 (S)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800475 GCST90264187 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine (S)-3-hydroxybutyrylcarnitine levels in chronic kidney disease 4,816 European ancestry individuals NA Illumina [7723044] (imputed) 0 (S)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800475 GCST90264188 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine (S)-a-Amino-omega-caprolactam levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723506] (imputed) 0 (S)-a-amino-omega-caprolactam measurement http://www.ebi.ac.uk/efo/EFO_0801055 GCST90264189 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-oleoyl)-GPE (P-18:1)* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 1-(1-enyl-oleoyl)-GPE (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800359 GCST90264190 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90264191 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264192 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4)* levels in chronic kidney disease 2,730 European ancestry individuals NA Illumina [7723486] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264193 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264194 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264195 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800420 GCST90264196 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1)* levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723893] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264197 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800466 GCST90264198 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine lactose levels in chronic kidney disease 4,887 European ancestry individuals NA Illumina [7724543] (imputed) 1 lactose measurement http://www.ebi.ac.uk/efo/EFO_0010507 GCST90265429 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lactosyl-N-behenoyl-sphingosine (d18:1/22:0)* levels in chronic kidney disease 4,401 European ancestry individuals NA Illumina [7724858] (imputed) 1 lactosyl-N-behenoyl-sphingosine (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800518 GCST90265430 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lactosyl-N-nervonoyl-sphingosine (d18:1/24:1)* levels in chronic kidney disease 4,945 European ancestry individuals NA Illumina [7724525] (imputed) 1 lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800517 GCST90265431 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 1 lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800429 GCST90265432 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lanthionine levels in chronic kidney disease 4,349 European ancestry individuals NA Illumina [7724715] (imputed) 0 lanthionine measurement http://www.ebi.ac.uk/efo/EFO_0800063 GCST90265433 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine lanthionine levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723545] (imputed) 0 lanthionine measurement http://www.ebi.ac.uk/efo/EFO_0800063 GCST90265434 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma laurate (12:0) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90265435 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma laurylcarnitine (C12) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90265436 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine laurylcarnitine (C12) levels in chronic kidney disease 3,997 European ancestry individuals NA Illumina [7724403] (imputed) 1 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90265437 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma leucine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90265438 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine leucine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90265439 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma leucylglycine levels in chronic kidney disease 2,652 European ancestry individuals NA Illumina [7721371] (imputed) 0 leucylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800678 GCST90265440 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma levulinate (4-oxovalerate) levels in chronic kidney disease 3,708 European ancestry individuals NA Illumina [7722367] (imputed) 0 levulinate 4-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021024 GCST90265441 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine levulinate (4-oxovalerate) levels in chronic kidney disease 4,300 European ancestry individuals NA Illumina [7724471] (imputed) 1 levulinate 4-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021024 GCST90265442 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma levulinoylcarnitine levels in chronic kidney disease 3,804 European ancestry individuals NA Illumina [7723532] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265443 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine levulinoylcarnitine levels in chronic kidney disease 4,843 European ancestry individuals NA Illumina [7724288] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265444 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lignoceroyl sphingomyelin (d18:1/24:0) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 lignoceroyl sphingomyelin (d18:1/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800377 GCST90265445 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lignoceroylcarnitine (C24)* levels in chronic kidney disease 4,949 European ancestry individuals NA Illumina [7724678] (imputed) 2 lignoceroylcarnitine (C24) measurement http://www.ebi.ac.uk/efo/EFO_0800541 GCST90265446 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine linamarin levels in chronic kidney disease 1,010 European ancestry individuals NA Illumina [7718639] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265447 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linoleamide (18:2n6) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90265448 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linoleate (18:2n6) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90265449 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linolenamide (18:3)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265450 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linolenate [alpha or gamma; (18:3n3 or 6)] levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90265451 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linolenoylcarnitine (C18:3)* levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7724019] (imputed) 1 linolenoylcarnitine (C18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800538 GCST90265452 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1]* levels in chronic kidney disease 4,526 European ancestry individuals NA Illumina [7724557] (imputed) 2 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800499 GCST90265453 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma imidazole lactate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 4 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90265379 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine imidazole lactate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 2 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90265380 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma imidazole propionate levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723777] (imputed) 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90265381 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine imidazole propionate levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723566] (imputed) 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90265382 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma iminodiacetate (IDA) levels in chronic kidney disease 4,936 European ancestry individuals NA Illumina [7724459] (imputed) 0 iminodiacetate (IDA) measurement http://www.ebi.ac.uk/efo/EFO_0800945 GCST90265383 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma indole-3-carboxylate levels in chronic kidney disease 2,613 European ancestry individuals NA Illumina [7722852] (imputed) 0 indole-3-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800043 GCST90265384 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indole-3-carboxylate levels in chronic kidney disease 3,814 European ancestry individuals NA Illumina [7724579] (imputed) 0 indole-3-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800043 GCST90265385 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma indoleacetate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90265386 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indoleacetate levels in chronic kidney disease 4,896 European ancestry individuals NA Illumina [7724455] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90265387 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma indoleacetoylcarnitine* levels in chronic kidney disease 4,413 European ancestry individuals NA Illumina [7723535] (imputed) 1 indoleacetoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800106 GCST90265388 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indoleacetoylcarnitine* levels in chronic kidney disease 4,217 European ancestry individuals NA Illumina [7723788] (imputed) 2 indoleacetoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800106 GCST90265389 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma indoleacetylglutamine levels in chronic kidney disease 4,661 European ancestry individuals NA Illumina [7723656] (imputed) 2 indoleacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800035 GCST90265390 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indoleacetylglutamine levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723706] (imputed) 2 indoleacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800035 GCST90265391 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indoleacetylglycine levels in chronic kidney disease 4,217 European ancestry individuals NA Illumina [7723552] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265392 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma indolelactate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90265393 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indolelactate levels in chronic kidney disease 4,902 European ancestry individuals NA Illumina [7723542] (imputed) 2 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90265394 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma indolepropionate levels in chronic kidney disease 4,866 European ancestry individuals NA Illumina [7723447] (imputed) 1 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90265395 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma indolepropionylglycine levels in chronic kidney disease 2,067 European ancestry individuals NA Illumina [7722369] (imputed) 0 indolepropionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800089 GCST90265396 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indolepropionylglycine levels in chronic kidney disease 4,861 European ancestry individuals NA Illumina [7723644] (imputed) 2 indolepropionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800089 GCST90265397 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indolin-2-one levels in chronic kidney disease 4,855 European ancestry individuals NA Illumina [7723724] (imputed) 0 indolin-2-one measurement http://www.ebi.ac.uk/efo/EFO_0800981 GCST90265398 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine indoxyl glucuronide levels in chronic kidney disease 4,886 European ancestry individuals NA Illumina [7724586] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265399 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma inosine levels in chronic kidney disease 3,202 European ancestry individuals NA Illumina [7721775] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90265400 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine inosine levels in chronic kidney disease 4,874 European ancestry individuals NA Illumina [7723492] (imputed) 1 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90265401 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma isobutyrylcarnitine (C4) levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723858] (imputed) 2 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90265402 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isobutyrylcarnitine (C4) levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723631] (imputed) 1 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90265403 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dexpanthenol levels in chronic kidney disease 1,810 European ancestry individuals NA Illumina [7721752] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265016 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dexpanthenol levels in chronic kidney disease 3,656 European ancestry individuals NA Illumina [7722274] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265017 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine diacetylspermidine* levels in chronic kidney disease 4,840 European ancestry individuals NA Illumina [7723762] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265018 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma diacylglycerol (14:0/18:1, 16:0/16:1) [1]* levels in chronic kidney disease 1,010 European ancestry individuals NA Illumina [7720438] (imputed) 0 diacylglycerol (14:0/18:1, 16:0/16:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800505 GCST90265019 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma diacylglycerol (14:0/18:1, 16:0/16:1) [2]* levels in chronic kidney disease 1,310 European ancestry individuals NA Illumina [7719345] (imputed) 0 diacylglycerol (14:0/18:1, 16:0/16:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800506 GCST90265020 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma diacylglycerol (16:1/18:2 [2], 16:0/18:3 [1])* levels in chronic kidney disease 4,670 European ancestry individuals NA Illumina [7723909] (imputed) 0 diacylglycerol (16:1/18:2 [2], 16:0/18:3 [1]) measurement http://www.ebi.ac.uk/efo/EFO_0800509 GCST90265021 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine diaminopimelate levels in chronic kidney disease 2,691 European ancestry individuals NA Illumina [7725774] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265022 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine diethanolamine levels in chronic kidney disease 4,603 European ancestry individuals NA Illumina [7723576] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265023 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine digalactosylglycerol* levels in chronic kidney disease 1,833 European ancestry individuals NA Illumina [7727103] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265024 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma diglycerol levels in chronic kidney disease 1,602 European ancestry individuals NA Illumina [7720669] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265025 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine diglycerol levels in chronic kidney disease 2,005 European ancestry individuals NA Illumina [7721059] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265026 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihomo-linoleate (20:2n6) levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723807] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90265027 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihomo-linolenate (20:3n3 or n6) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90265028 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihomo-linolenoyl-choline levels in chronic kidney disease 4,289 European ancestry individuals NA Illumina [7724422] (imputed) 0 dihomo-linolenoyl-choline measurement http://www.ebi.ac.uk/efo/EFO_0800481 GCST90265029 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihomo-linolenoylcarnitine (C20:3n3 or 6)* levels in chronic kidney disease 4,846 European ancestry individuals NA Illumina [7724807] (imputed) 2 dihomo-linolenoylcarnitine (C20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800547 GCST90265030 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihomo-linoleoylcarnitine (C20:2)* levels in chronic kidney disease 4,404 European ancestry individuals NA Illumina [7723309] (imputed) 1 dihomo-linoleoylcarnitine (C20:2) measurement http://www.ebi.ac.uk/efo/EFO_0800546 GCST90265031 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dihydrobiopterin levels in chronic kidney disease 3,644 European ancestry individuals NA Illumina [7723843] (imputed) 0 dihydrobiopterin measurement http://www.ebi.ac.uk/efo/EFO_0801076 GCST90265032 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihydrocaffeate sulfate (2) levels in chronic kidney disease 4,725 European ancestry individuals NA Illumina [7724236] (imputed) 0 dihydrocaffeate sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801044 GCST90265033 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihydroferulate levels in chronic kidney disease 3,248 European ancestry individuals NA Illumina [7724808] (imputed) 0 dihydroferulate measurement http://www.ebi.ac.uk/efo/EFO_0800969 GCST90265034 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dihydroferulate levels in chronic kidney disease 4,439 European ancestry individuals NA Illumina [7725143] (imputed) 0 dihydroferulate measurement http://www.ebi.ac.uk/efo/EFO_0800969 GCST90265035 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihydroferulic acid sulfate levels in chronic kidney disease 2,902 European ancestry individuals NA Illumina [7723194] (imputed) 0 dihydroferulic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801026 GCST90265036 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dihydroferulic acid sulfate levels in chronic kidney disease 4,905 European ancestry individuals NA Illumina [7723641] (imputed) 1 dihydroferulic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801026 GCST90265037 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dihydroorotate levels in chronic kidney disease 4,763 European ancestry individuals NA Illumina [7722595] (imputed) 1 dihydroorotate measurement http://www.ebi.ac.uk/efo/EFO_0800647 GCST90265038 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dihydroorotate levels in chronic kidney disease 4,069 European ancestry individuals NA Illumina [7723058] (imputed) 0 dihydroorotate measurement http://www.ebi.ac.uk/efo/EFO_0800647 GCST90265039 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dimethyl sulfone levels in chronic kidney disease 4,316 European ancestry individuals NA Illumina [7722901] (imputed) 0 dimethyl sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800979 GCST90265040 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isobutyrylglycine levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7723778] (imputed) 2 isobutyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800029 GCST90265404 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isocaproylglutamine levels in chronic kidney disease 4,900 European ancestry individuals NA Illumina [7723995] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265405 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isocaproylglycine levels in chronic kidney disease 4,903 European ancestry individuals NA Illumina [7723573] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265406 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isocitrate levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 isocitrate measurement http://www.ebi.ac.uk/efo/EFO_0010505 GCST90265407 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isocitric lactone levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723627] (imputed) 1 isocitric lactone measurement http://www.ebi.ac.uk/efo/EFO_0800180 GCST90265408 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma isoeugenol sulfate levels in chronic kidney disease 4,034 European ancestry individuals NA Illumina [7722810] (imputed) 0 isoeugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800993 GCST90265409 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isoeugenol sulfate levels in chronic kidney disease 4,599 European ancestry individuals NA Illumina [7723741] (imputed) 0 isoeugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800993 GCST90265410 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma isoleucine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90265411 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isoleucine levels in chronic kidney disease 1,621 European ancestry individuals NA Illumina [7721669] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90265412 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma isoursodeoxycholate levels in chronic kidney disease 4,885 European ancestry individuals NA Illumina [7724397] (imputed) 0 isoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800315 GCST90265413 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma isoursodeoxycholate sulfate (1) levels in chronic kidney disease 1,367 European ancestry individuals NA Illumina [7724331] (imputed) 0 isoursodeoxycholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800595 GCST90265414 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma isovalerylcarnitine (C5) levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 isovalerylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800024 GCST90265415 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isovalerylcarnitine (C5) levels in chronic kidney disease 2,747 European ancestry individuals NA Illumina [7725316] (imputed) 0 isovalerylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800024 GCST90265416 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isovalerylglutamine levels in chronic kidney disease 4,891 European ancestry individuals NA Illumina [7724228] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265417 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma isovalerylglycine levels in chronic kidney disease 3,635 European ancestry individuals NA Illumina [7724175] (imputed) 0 isovalerylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800025 GCST90265418 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isovalerylglycine levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723643] (imputed) 1 isovalerylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800025 GCST90265419 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine isoxanthopterin levels in chronic kidney disease 4,134 European ancestry individuals NA Illumina [7723614] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265420 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma kynurenate levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90265421 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine kynurenate levels in chronic kidney disease 4,910 European ancestry individuals NA Illumina [7723600] (imputed) 1 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90265422 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma kynurenine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90265423 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine kynurenine levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723707] (imputed) 3 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90265424 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma L-urobilin levels in chronic kidney disease 1,805 European ancestry individuals NA Illumina [7721449] (imputed) 0 L-urobilin measurement http://www.ebi.ac.uk/efo/EFO_0800161 GCST90265425 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine L-urobilin levels in chronic kidney disease 2,964 European ancestry individuals NA Illumina [7720409] (imputed) 0 L-urobilin measurement http://www.ebi.ac.uk/efo/EFO_0800161 GCST90265426 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lactate levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723804] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90265427 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine lactate levels in chronic kidney disease 4,514 European ancestry individuals NA Illumina [7725031] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90265428 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma creatinine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90264966 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine creatinine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90264967 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cryptochlorogenic acid levels in chronic kidney disease 1,201 European ancestry individuals NA Illumina [7720029] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264968 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cyclo(leu-asp)* levels in chronic kidney disease 4,777 European ancestry individuals NA Illumina [7723618] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264969 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cyclo(pro-arg)* levels in chronic kidney disease 4,904 European ancestry individuals NA Illumina [7723620] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264970 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cyclo(pro-sulfo-tyr)* levels in chronic kidney disease 4,901 European ancestry individuals NA Illumina [7724062] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264971 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cyclo(pro-val) (D,L)* levels in chronic kidney disease 3,135 European ancestry individuals NA Illumina [7723527] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264972 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cys-gly, oxidized levels in chronic kidney disease 4,957 European ancestry individuals NA Illumina [7723836] (imputed) 2 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90264973 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cystathionine levels in chronic kidney disease 4,881 European ancestry individuals NA Illumina [7724016] (imputed) 1 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90264974 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cystathionine levels in chronic kidney disease 4,628 European ancestry individuals NA Illumina [7724255] (imputed) 1 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90264975 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cysteine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90264976 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cysteine s-sulfate levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723615] (imputed) 0 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90264977 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cysteine s-sulfate levels in chronic kidney disease 4,875 European ancestry individuals NA Illumina [7724064] (imputed) 0 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90264978 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cysteine sulfinic acid levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723726] (imputed) 0 cysteine sulfinic acid measurement http://www.ebi.ac.uk/efo/EFO_0800041 GCST90264979 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cysteine levels in chronic kidney disease 4,908 European ancestry individuals NA Illumina [7723409] (imputed) 1 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90264980 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cysteine-glutathione disulfide levels in chronic kidney disease 4,843 European ancestry individuals NA Illumina [7724578] (imputed) 0 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90264981 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cysteinylglycine disulfide* levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 2 cysteinylglycine disulfide measurement http://www.ebi.ac.uk/efo/EFO_0800049 GCST90264982 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cysteinylglycine disulfide* levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723644] (imputed) 1 cysteinylglycine disulfide measurement http://www.ebi.ac.uk/efo/EFO_0800049 GCST90264983 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cysteinylglycine levels in chronic kidney disease 4,803 European ancestry individuals NA Illumina [7723041] (imputed) 1 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90264984 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cysteinylglycine levels in chronic kidney disease 4,688 European ancestry individuals NA Illumina [7724359] (imputed) 2 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90264985 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cystine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90264986 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cystine levels in chronic kidney disease 4,825 European ancestry individuals NA Illumina [7723407] (imputed) 1 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90264987 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cytidine levels in chronic kidney disease 4,739 European ancestry individuals NA Illumina [7724484] (imputed) 1 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90264988 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cytosine levels in chronic kidney disease 4,892 European ancestry individuals NA Illumina [7724327] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264989 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine daidzein 7-O-glucuronide levels in chronic kidney disease 1,797 European ancestry individuals NA Illumina [7728685] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264990 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2]* levels in chronic kidney disease 4,527 European ancestry individuals NA Illumina [7724670] (imputed) 2 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800500 GCST90265454 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linoleoyl-linoleoyl-glycerol (18:2/18:2) [1]* levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7724458] (imputed) 1 linoleoyl-linoleoyl-glycerol (18:2/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800510 GCST90265455 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linoleoylcarnitine (C18:2)* levels in chronic kidney disease 4,959 European ancestry individuals NA Illumina [7723843] (imputed) 2 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90265456 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma linoleoylcholine* levels in chronic kidney disease 4,927 European ancestry individuals NA Illumina [7723875] (imputed) 0 linoleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800535 GCST90265457 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lithocholate sulfate (1) levels in chronic kidney disease 4,019 European ancestry individuals NA Illumina [7721570] (imputed) 1 lithocholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800579 GCST90265458 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lysine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90265459 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine lysine levels in chronic kidney disease 4,911 European ancestry individuals NA Illumina [7723632] (imputed) 1 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90265460 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma lyxonate levels in chronic kidney disease 4,932 European ancestry individuals NA Illumina [7724403] (imputed) 0 lyxonate measurement http://www.ebi.ac.uk/efo/EFO_0800150 GCST90265461 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine lyxonate levels in chronic kidney disease 4,909 European ancestry individuals NA Illumina [7723584] (imputed) 0 lyxonate measurement http://www.ebi.ac.uk/efo/EFO_0800150 GCST90265462 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma m-tyramine sulfate levels in chronic kidney disease 1,952 European ancestry individuals NA Illumina [7724300] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265463 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine m-tyramine sulfate levels in chronic kidney disease 4,873 European ancestry individuals NA Illumina [7724083] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265464 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine m-tyramine levels in chronic kidney disease 4,647 European ancestry individuals NA Illumina [7725243] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265465 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cortolone glucuronide (1) levels in chronic kidney disease 4,897 European ancestry individuals NA Illumina [7724648] (imputed) 0 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90264953 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cortolone glucuronide (2) levels in chronic kidney disease 4,770 European ancestry individuals NA Illumina [7723798] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264954 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cotinine N-oxide levels in chronic kidney disease 867 European ancestry individuals NA Illumina [7727801] (imputed) 0 cotinine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0800965 GCST90264955 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cotinine N-oxide levels in chronic kidney disease 835 European ancestry individuals NA Illumina [7735542] (imputed) 0 cotinine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0800965 GCST90264956 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma cotinine levels in chronic kidney disease 1,885 European ancestry individuals NA Illumina [7731279] (imputed) 0 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST90264957 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine cotinine levels in chronic kidney disease 1,015 European ancestry individuals NA Illumina [7728519] (imputed) 0 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST90264958 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine coumaroylquinate (1) levels in chronic kidney disease 3,801 European ancestry individuals NA Illumina [7723352] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264959 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine coumaroylquinate (2) levels in chronic kidney disease 3,942 European ancestry individuals NA Illumina [7725039] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264960 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine coumaroylquinate (3) levels in chronic kidney disease 2,696 European ancestry individuals NA Illumina [7724978] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264961 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine coumaroylquinate (4) levels in chronic kidney disease 3,887 European ancestry individuals NA Illumina [7724919] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264962 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine coumaroylquinate (5) levels in chronic kidney disease 3,560 European ancestry individuals NA Illumina [7723544] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264963 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma creatine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90264964 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine creatine levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90264965 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine daidzein sulfate (1) levels in chronic kidney disease 578 European ancestry individuals NA Illumina [7731469] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264991 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma daidzein sulfate (2) levels in chronic kidney disease 522 European ancestry individuals NA Illumina [7725483] (imputed) 0 daidzein sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801007 GCST90264992 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine daidzein sulfate (2) levels in chronic kidney disease 1,437 European ancestry individuals NA Illumina [7728535] (imputed) 0 daidzein sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801007 GCST90264993 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine daidzein levels in chronic kidney disease 878 European ancestry individuals NA Illumina [7726200] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264994 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma decadienedioic acid (C10:2-DC)** levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7724396] (imputed) 1 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90264995 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine decadienedioic acid (C10:2-DC)** levels in chronic kidney disease 4,872 European ancestry individuals NA Illumina [7723733] (imputed) 1 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90264996 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma decanoylcarnitine (C10) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723828] (imputed) 2 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90264997 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine decanoylcarnitine (C10) levels in chronic kidney disease 4,344 European ancestry individuals NA Illumina [7724825] (imputed) 1 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90264998 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dehydroandrosterone glucuronide levels in chronic kidney disease 4,821 European ancestry individuals NA Illumina [7723837] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90264999 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dehydroascorbate levels in chronic kidney disease 3,648 European ancestry individuals NA Illumina [7724127] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265000 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dehydroepiandrosterone glucuronide levels in chronic kidney disease 2,799 European ancestry individuals NA Illumina [7724437] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265001 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma dehydroepiandrosterone sulfate (DHEA-S) levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723785] (imputed) 1 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90265002 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine dehydroepiandrosterone sulfate (DHEA-S) levels in chronic kidney disease 4,565 European ancestry individuals NA Illumina [7723764] (imputed) 0 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90265003 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine delta-CEHC glucuronide levels in chronic kidney disease 962 European ancestry individuals NA Illumina [7724042] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265004 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine delta-CEHC sulfate levels in chronic kidney disease 1,401 European ancestry individuals NA Illumina [7725360] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265005 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine delta-CEHC levels in chronic kidney disease 1,699 European ancestry individuals NA Illumina [7727701] (imputed) 0 delta-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800174 GCST90265006 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma deoxycarnitine levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 1 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90265007 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine deoxycarnitine levels in chronic kidney disease 4,878 European ancestry individuals NA Illumina [7724458] (imputed) 0 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90265008 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma deoxycholate levels in chronic kidney disease 3,913 European ancestry individuals NA Illumina [7723483] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90265009 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine deoxycholate levels in chronic kidney disease 2,306 European ancestry individuals NA Illumina [7719983] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90265010 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma deoxycholic acid 12-sulfate* levels in chronic kidney disease 3,412 European ancestry individuals NA Illumina [7722885] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265011 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine deoxycholic acid 12-sulfate* levels in chronic kidney disease 3,885 European ancestry individuals NA Illumina [7722751] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90265012 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine deoxycholic acid 3-sulfate levels in chronic kidney disease 1,361 European ancestry individuals NA Illumina [7719232] (imputed) 0 deoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800383 GCST90265013 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma deoxycholic acid glucuronide levels in chronic kidney disease 4,692 European ancestry individuals NA Illumina [7724490] (imputed) 1 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90265014 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine deoxycholic acid glucuronide levels in chronic kidney disease 3,792 European ancestry individuals NA Illumina [7722860] (imputed) 1 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90265015 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21441 levels in chronic kidney disease 4,051 European ancestry individuals NA Illumina [7722626] (imputed) 2 X-21441 measurement http://www.ebi.ac.uk/efo/EFO_0800814 GCST90266501 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21441 levels in chronic kidney disease 2,409 European ancestry individuals NA Illumina [7721130] (imputed) 0 X-21441 measurement http://www.ebi.ac.uk/efo/EFO_0800814 GCST90266502 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21442 levels in chronic kidney disease 4,428 European ancestry individuals NA Illumina [7723890] (imputed) 0 X-21442 measurement http://www.ebi.ac.uk/efo/EFO_0800815 GCST90266503 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21467 levels in chronic kidney disease 4,412 European ancestry individuals NA Illumina [7723405] (imputed) 2 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90266504 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21467 levels in chronic kidney disease 4,243 European ancestry individuals NA Illumina [7724435] (imputed) 2 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90266505 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21470 levels in chronic kidney disease 4,212 European ancestry individuals NA Illumina [7723101] (imputed) 2 X-21470 measurement http://www.ebi.ac.uk/efo/EFO_0800817 GCST90266506 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21470 levels in chronic kidney disease 4,221 European ancestry individuals NA Illumina [7722618] (imputed) 2 X-21470 measurement http://www.ebi.ac.uk/efo/EFO_0800817 GCST90266507 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21471 levels in chronic kidney disease 3,964 European ancestry individuals NA Illumina [7721810] (imputed) 2 X-21471 measurement http://www.ebi.ac.uk/efo/EFO_0800818 GCST90266508 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21607 levels in chronic kidney disease 4,540 European ancestry individuals NA Illumina [7723536] (imputed) 3 X-21607 measurement http://www.ebi.ac.uk/efo/EFO_0800819 GCST90266509 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21661 levels in chronic kidney disease 2,097 European ancestry individuals NA Illumina [7727961] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266510 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21733 levels in chronic kidney disease 3,643 European ancestry individuals NA Illumina [7725425] (imputed) 0 X-21733 measurement http://www.ebi.ac.uk/efo/EFO_0800820 GCST90266511 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21787 levels in chronic kidney disease 3,721 European ancestry individuals NA Illumina [7722856] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266517 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21796 levels in chronic kidney disease 4,706 European ancestry individuals NA Illumina [7724213] (imputed) 1 X-21796 measurement http://www.ebi.ac.uk/efo/EFO_0800825 GCST90266519 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21803 levels in chronic kidney disease 3,320 European ancestry individuals NA Illumina [7722117] (imputed) 0 X-21803 measurement http://www.ebi.ac.uk/efo/EFO_0800826 GCST90266521 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21807 levels in chronic kidney disease 3,243 European ancestry individuals NA Illumina [7723548] (imputed) 0 X-21807 measurement http://www.ebi.ac.uk/efo/EFO_0800827 GCST90266523 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21807 levels in chronic kidney disease 4,791 European ancestry individuals NA Illumina [7724865] (imputed) 0 X-21807 measurement http://www.ebi.ac.uk/efo/EFO_0800827 GCST90266524 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21815 levels in chronic kidney disease 4,863 European ancestry individuals NA Illumina [7723578] (imputed) 0 X-21815 measurement http://www.ebi.ac.uk/efo/EFO_0800828 GCST90266526 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21816 levels in chronic kidney disease 1,753 European ancestry individuals NA Illumina [7720724] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266527 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21816 levels in chronic kidney disease 2,248 European ancestry individuals NA Illumina [7725567] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266528 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21821 levels in chronic kidney disease 3,965 European ancestry individuals NA Illumina [7722504] (imputed) 0 X-21821 measurement http://www.ebi.ac.uk/efo/EFO_0800829 GCST90266529 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21821 levels in chronic kidney disease 4,907 European ancestry individuals NA Illumina [7723517] (imputed) 0 X-21821 measurement http://www.ebi.ac.uk/efo/EFO_0800829 GCST90266530 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21825 levels in chronic kidney disease 4,467 European ancestry individuals NA Illumina [7722917] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266531 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21827 levels in chronic kidney disease 4,453 European ancestry individuals NA Illumina [7722329] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266532 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21828 levels in chronic kidney disease 3,979 European ancestry individuals NA Illumina [7721527] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266533 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21829 levels in chronic kidney disease 4,817 European ancestry individuals NA Illumina [7723449] (imputed) 2 X-21829 measurement http://www.ebi.ac.uk/efo/EFO_0800830 GCST90266534 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21830 levels in chronic kidney disease 4,906 European ancestry individuals NA Illumina [7723628] (imputed) 0 X-21830 measurement http://www.ebi.ac.uk/efo/EFO_0800831 GCST90266535 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21831 levels in chronic kidney disease 4,599 European ancestry individuals NA Illumina [7723693] (imputed) 1 X-21831 measurement http://www.ebi.ac.uk/efo/EFO_0800832 GCST90266536 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21834 levels in chronic kidney disease 4,135 European ancestry individuals NA Illumina [7723868] (imputed) 0 X-21834 measurement http://www.ebi.ac.uk/efo/EFO_0800833 GCST90266537 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21834 levels in chronic kidney disease 4,495 European ancestry individuals NA Illumina [7724154] (imputed) 0 X-21834 measurement http://www.ebi.ac.uk/efo/EFO_0800833 GCST90266538 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21838 levels in chronic kidney disease 1,055 European ancestry individuals NA Illumina [7720504] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266539 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21839 levels in chronic kidney disease 2,654 European ancestry individuals NA Illumina [7719854] (imputed) 0 X-21839 measurement http://www.ebi.ac.uk/efo/EFO_0800834 GCST90266540 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21839 levels in chronic kidney disease 3,961 European ancestry individuals NA Illumina [7721337] (imputed) 0 X-21839 measurement http://www.ebi.ac.uk/efo/EFO_0800834 GCST90266541 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21840 levels in chronic kidney disease 1,871 European ancestry individuals NA Illumina [7724047] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266542 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21840 levels in chronic kidney disease 4,804 European ancestry individuals NA Illumina [7722570] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266543 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21841 levels in chronic kidney disease 4,801 European ancestry individuals NA Illumina [7723938] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266544 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21842 levels in chronic kidney disease 1,726 European ancestry individuals NA Illumina [7722933] (imputed) 0 X-21842 measurement http://www.ebi.ac.uk/efo/EFO_0800835 GCST90266545 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21842 levels in chronic kidney disease 4,056 European ancestry individuals NA Illumina [7723773] (imputed) 1 X-21842 measurement http://www.ebi.ac.uk/efo/EFO_0800835 GCST90266546 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21845 levels in chronic kidney disease 3,041 European ancestry individuals NA Illumina [7721597] (imputed) 0 X-21845 measurement http://www.ebi.ac.uk/efo/EFO_0800836 GCST90266547 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21845 levels in chronic kidney disease 4,085 European ancestry individuals NA Illumina [7721930] (imputed) 0 X-21845 measurement http://www.ebi.ac.uk/efo/EFO_0800836 GCST90266548 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21847 levels in chronic kidney disease 3,414 European ancestry individuals NA Illumina [7721262] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266549 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21851 levels in chronic kidney disease 4,813 European ancestry individuals NA Illumina [7723747] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266550 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X - 19913 levels in chronic kidney disease 4,888 European ancestry individuals NA Illumina [7724126] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266476 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21258 levels in chronic kidney disease 4,954 European ancestry individuals NA Illumina [7723800] (imputed) 1 X-21258 measurement http://www.ebi.ac.uk/efo/EFO_0800802 GCST90266477 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21258 levels in chronic kidney disease 4,784 European ancestry individuals NA Illumina [7724212] (imputed) 1 X-21258 measurement http://www.ebi.ac.uk/efo/EFO_0800802 GCST90266478 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21283 levels in chronic kidney disease 4,053 European ancestry individuals NA Illumina [7724869] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266479 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21283 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266480 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21285 levels in chronic kidney disease 4,202 European ancestry individuals NA Illumina [7723936] (imputed) 0 X-21285 measurement http://www.ebi.ac.uk/efo/EFO_0800803 GCST90266481 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21286 levels in chronic kidney disease 4,702 European ancestry individuals NA Illumina [7723795] (imputed) 0 X-21286 measurement http://www.ebi.ac.uk/efo/EFO_0800804 GCST90266482 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21286 levels in chronic kidney disease 4,295 European ancestry individuals NA Illumina [7724737] (imputed) 1 X-21286 measurement http://www.ebi.ac.uk/efo/EFO_0800804 GCST90266483 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21310 levels in chronic kidney disease 4,922 European ancestry individuals NA Illumina [7724301] (imputed) 0 X-21310 measurement http://www.ebi.ac.uk/efo/EFO_0800805 GCST90266484 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21310 levels in chronic kidney disease 3,516 European ancestry individuals NA Illumina [7723397] (imputed) 0 X-21310 measurement http://www.ebi.ac.uk/efo/EFO_0800805 GCST90266485 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21312 levels in chronic kidney disease 3,862 European ancestry individuals NA Illumina [7722301] (imputed) 0 X-21312 measurement http://www.ebi.ac.uk/efo/EFO_0800806 GCST90266486 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21319 levels in chronic kidney disease 4,890 European ancestry individuals NA Illumina [7723930] (imputed) 0 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90266487 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21319 levels in chronic kidney disease 2,828 European ancestry individuals NA Illumina [7723020] (imputed) 0 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90266488 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21339 levels in chronic kidney disease 4,280 European ancestry individuals NA Illumina [7724194] (imputed) 1 X-21339 measurement http://www.ebi.ac.uk/efo/EFO_0800808 GCST90266489 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21342 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266490 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21351 levels in chronic kidney disease 4,597 European ancestry individuals NA Illumina [7724874] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266491 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21353 levels in chronic kidney disease 4,956 European ancestry individuals NA Illumina [7723813] (imputed) 1 X-21353 measurement http://www.ebi.ac.uk/efo/EFO_0800809 GCST90266492 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21355 levels in chronic kidney disease 4,960 European ancestry individuals NA Illumina [7723840] (imputed) 0 X-21355 measurement http://www.ebi.ac.uk/efo/EFO_0800810 GCST90266493 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21360 levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723899] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266494 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21362 levels in chronic kidney disease 4,952 European ancestry individuals NA Illumina [7723679] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266495 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21364 levels in chronic kidney disease 4,676 European ancestry individuals NA Illumina [7723449] (imputed) 0 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90266496 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21364 levels in chronic kidney disease 3,675 European ancestry individuals NA Illumina [7721894] (imputed) 0 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90266497 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21383 levels in chronic kidney disease 3,776 European ancestry individuals NA Illumina [7723994] (imputed) 0 X-21383 measurement http://www.ebi.ac.uk/efo/EFO_0800812 GCST90266498 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21410 levels in chronic kidney disease 3,785 European ancestry individuals NA Illumina [7723107] (imputed) 1 X-21410 measurement http://www.ebi.ac.uk/efo/EFO_0800813 GCST90266499 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21410 levels in chronic kidney disease 4,794 European ancestry individuals NA Illumina [7724629] (imputed) 1 X-21410 measurement http://www.ebi.ac.uk/efo/EFO_0800813 GCST90266500 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21736 levels in chronic kidney disease 4,955 European ancestry individuals NA Illumina [7723843] (imputed) 0 X-21736 measurement http://www.ebi.ac.uk/efo/EFO_0800821 GCST90266512 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21736 levels in chronic kidney disease 4,682 European ancestry individuals NA Illumina [7723836] (imputed) 0 X-21736 measurement http://www.ebi.ac.uk/efo/EFO_0800821 GCST90266513 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21740 levels in chronic kidney disease 4,606 European ancestry individuals NA Illumina [7722779] (imputed) 0 X-21740 measurement http://www.ebi.ac.uk/efo/EFO_0800822 GCST90266514 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21742 levels in chronic kidney disease 2,775 European ancestry individuals NA Illumina [7723815] (imputed) 0 X-21742 measurement http://www.ebi.ac.uk/efo/EFO_0800823 GCST90266515 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21752 levels in chronic kidney disease 896 European ancestry individuals NA Illumina [7729222] (imputed) 0 X-21752 measurement http://www.ebi.ac.uk/efo/EFO_0800824 GCST90266516 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21788 levels in chronic kidney disease 4,892 European ancestry individuals NA Illumina [7724301] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266518 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21796 levels in chronic kidney disease 4,912 European ancestry individuals NA Illumina [7723603] (imputed) 1 X-21796 measurement http://www.ebi.ac.uk/efo/EFO_0800825 GCST90266520 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-21803 levels in chronic kidney disease 4,816 European ancestry individuals NA Illumina [7724105] (imputed) 0 X-21803 measurement http://www.ebi.ac.uk/efo/EFO_0800826 GCST90266522 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-21815 levels in chronic kidney disease 2,689 European ancestry individuals NA Illumina [7725117] (imputed) 0 X-21815 measurement http://www.ebi.ac.uk/efo/EFO_0800828 GCST90266525 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18410 levels in chronic kidney disease 2,834 European ancestry individuals NA Illumina [7723280] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266452 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18750 levels in chronic kidney disease 615 European ancestry individuals NA Illumina [7724240] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266453 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18779 levels in chronic kidney disease 4,826 European ancestry individuals NA Illumina [7723814] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266454 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18838 levels in chronic kidney disease 4,843 European ancestry individuals NA Illumina [7724436] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266455 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18886 levels in chronic kidney disease 4,306 European ancestry individuals NA Illumina [7721901] (imputed) 0 X-18886 measurement http://www.ebi.ac.uk/efo/EFO_0800790 GCST90266456 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18886 levels in chronic kidney disease 4,861 European ancestry individuals NA Illumina [7723270] (imputed) 1 X-18886 measurement http://www.ebi.ac.uk/efo/EFO_0800790 GCST90266457 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18887 levels in chronic kidney disease 3,764 European ancestry individuals NA Illumina [7722671] (imputed) 0 X-18887 measurement http://www.ebi.ac.uk/efo/EFO_0800791 GCST90266458 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18887 levels in chronic kidney disease 4,826 European ancestry individuals NA Illumina [7724031] (imputed) 0 X-18887 measurement http://www.ebi.ac.uk/efo/EFO_0800791 GCST90266459 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18888 levels in chronic kidney disease 2,547 European ancestry individuals NA Illumina [7724205] (imputed) 0 X-18888 measurement http://www.ebi.ac.uk/efo/EFO_0800792 GCST90266460 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18888 levels in chronic kidney disease 4,877 European ancestry individuals NA Illumina [7723860] (imputed) 1 X-18888 measurement http://www.ebi.ac.uk/efo/EFO_0800792 GCST90266461 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18901 levels in chronic kidney disease 4,716 European ancestry individuals NA Illumina [7723701] (imputed) 0 X-18901 measurement http://www.ebi.ac.uk/efo/EFO_0800794 GCST90266462 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18913 levels in chronic kidney disease 4,958 European ancestry individuals NA Illumina [7723715] (imputed) 0 X-18913 measurement http://www.ebi.ac.uk/efo/EFO_0800795 GCST90266463 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18921 levels in chronic kidney disease 4,936 European ancestry individuals NA Illumina [7724271] (imputed) 2 X-18921 measurement http://www.ebi.ac.uk/efo/EFO_0800796 GCST90266464 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18922 levels in chronic kidney disease 4,719 European ancestry individuals NA Illumina [7722829] (imputed) 2 X-18922 measurement http://www.ebi.ac.uk/efo/EFO_0800797 GCST90266465 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-18935 levels in chronic kidney disease 2,143 European ancestry individuals NA Illumina [7722963] (imputed) 0 X-18935 measurement http://www.ebi.ac.uk/efo/EFO_0800798 GCST90266466 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18935 levels in chronic kidney disease 4,893 European ancestry individuals NA Illumina [7724654] (imputed) 1 X-18935 measurement http://www.ebi.ac.uk/efo/EFO_0800798 GCST90266467 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-18945 levels in chronic kidney disease 4,815 European ancestry individuals NA Illumina [7723260] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266468 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-19141 levels in chronic kidney disease 4,951 European ancestry individuals NA Illumina [7723896] (imputed) 2 X-19141 measurement http://www.ebi.ac.uk/efo/EFO_0800799 GCST90266469 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-19141 levels in chronic kidney disease 4,868 European ancestry individuals NA Illumina [7723856] (imputed) 1 X-19141 measurement http://www.ebi.ac.uk/efo/EFO_0800799 GCST90266470 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-19183 levels in chronic kidney disease 2,361 European ancestry individuals NA Illumina [7723249] (imputed) 0 X-19183 measurement http://www.ebi.ac.uk/efo/EFO_0800800 GCST90266471 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-19183 levels in chronic kidney disease 3,854 European ancestry individuals NA Illumina [7723756] (imputed) 0 X-19183 measurement http://www.ebi.ac.uk/efo/EFO_0800800 GCST90266472 Genome-wide genotyping array 2022-04-08 35278270 Forrest IS 2022-03-12 Eur J Heart Fail www.ncbi.nlm.nih.gov/pubmed/35278270 Genetic and phenotypic profiling of supranormal ejection fraction reveals decreased survival and underdiagnosed heart failure. Supranormal left ventricular ejection fraction 7,548 African ancestry, Hispanic, European ancestry, Asian ancestry, unknown ancestry cases, 23,009 African ancestry, Hispanic, European ancestry, Asian ancestry, unknown ancestry controls NA Affymetrix, Illumina [NR] (imputed) 16 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST90101736 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-19299 levels in chronic kidney disease 2,163 European ancestry individuals NA Illumina [7720303] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266473 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Plasma X-19438 levels in chronic kidney disease 3,450 European ancestry individuals NA Illumina [7723328] (imputed) 0 X-19438 measurement http://www.ebi.ac.uk/efo/EFO_0800801 GCST90266474 Genome-wide genotyping array 2023-06-22 37277652 Schlosser P 2023-06-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37277652 Genetic studies of paired metabolomes reveal enzymatic and transport processes at the interface of plasma and urine. Urine X-19763 levels in chronic kidney disease 1,263 European ancestry individuals NA Illumina [7724581] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90266475 Genome-wide genotyping array 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs population or mild symptoms) 48,880 European ancestry individuals NA Illumina [NR] 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104036 Genome-wide sequencing 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs population or mild symptoms) 48,880 European ancestry individuals NA Illumina [NR] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104037 Genome-wide sequencing 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs population or mild symptoms) 5,989 European ancestry cases, 42,891 European ancestry controls NA Illumina [8121457] 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104030 Genome-wide sequencing 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs population or mild symptoms) 788 South Asian ancestry cases, 3,793 South Asian ancestry controls NA Illumina [9092222] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104031 Genome-wide sequencing 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs population or mild symptoms) 440 African ancestry cases, 1,350 African ancestry controls NA Illumina [15012409] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104032 Genome-wide sequencing 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs population or mild symptoms) 274 East Asian ancestry cases, 366 East Asian ancestry controls NA Illumina [6000811] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104033 Genome-wide sequencing 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs population or mild symptoms) 5,989 European ancestry cases, 42,891 European ancestry controls, 788 South Asian ancestry cases, 3,793 South Asian ancestry controls, 440 African ancestry cases, 1,350 African ancestry controls, 274 East Asian ancestry cases, 366 East Asian ancestry controls NA Illumina [NR] 25 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104034 Genome-wide sequencing 2022-06-07 35255492 Kousathanas A 2022-03-07 Nature www.ncbi.nlm.nih.gov/pubmed/35255492 Whole genome sequencing reveals host factors underlying critical Covid-19. COVID-19 (critical illness vs mild symptoms) 5,989 European ancestry cases, 1,507 European ancestry controls NA Illumina [NR] 4 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104035 Genome-wide sequencing 2023-06-09 37079300 Ramo JT 2023-04-20 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/37079300 Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration. Central serous chorioretinopathy 552 Finnish ancestry cases, 343,461 Finnish ancestry controls NA Affymetrix, Illumina [13762498] (imputed) 1 central serous retinopathy http://www.ebi.ac.uk/efo/EFO_0009784 GCST90268400 Genome-wide genotyping array 2023-06-09 37079300 Ramo JT 2023-04-20 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/37079300 Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration. Central serous chorioretinopathy 103 European ancestry cases, 178,573 European ancestry controls NA Illumina [13694301] (imputed) 1 central serous retinopathy http://www.ebi.ac.uk/efo/EFO_0009784 GCST90268401 Genome-wide genotyping array 2023-06-09 37079300 Ramo JT 2023-04-20 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/37079300 Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular Degeneration. Central serous chorioretinopathy 1,176 European ancestry cases, 526,787 European ancestry controls NA Affymetrix, Illumina [12522976] (imputed) 5 central serous retinopathy http://www.ebi.ac.uk/efo/EFO_0009784 GCST90270255 Genome-wide genotyping array 2023-05-15 36587059 Libiseller-Egger J 2022-12-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36587059 Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes. Cardiovascular delta age (difference between ECG-predicted and chronological age) 34,432 European or unknown ancestry individuals NA NR [6357764] (imputed) 17 cardiovascular age measurement http://www.ebi.ac.uk/efo/EFO_0803380 GCST90255651 Genome-wide genotyping array 2023-05-15 36587059 Libiseller-Egger J 2022-12-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36587059 Deep learning-derived cardiovascular age shares a genetic basis with other cardiac phenotypes. Abnormal ECG 34,432 European or unknown ancestry individuals NA NR [6357764] (imputed) 2 Abnormal EKG http://purl.obolibrary.org/obo/HP_0003115 GCST90255652 Genome-wide genotyping array 2022-05-16 35174233 Park JB 2022-01-31 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/35174233 Genetic Determinants of Visit-to-Visit Lipid Variability: Genome-Wide Association Study in Statin-Naïve Korean Population. Low density lipoprotein cholesterol variability 4,287 Korean ancestry individuals 1,086 Korean ancestry individuals Affymetrix [NR] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90102616 Genome-wide genotyping array 2022-05-16 35174233 Park JB 2022-01-31 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/35174233 Genetic Determinants of Visit-to-Visit Lipid Variability: Genome-Wide Association Study in Statin-Naïve Korean Population. High density lipoprotein cholesterol variability 4,287 Korean ancestry individuals 1,086 Korean ancestry individuals Affymetrix [NR] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90102617 Genome-wide genotyping array 2022-01-19 34680357 Oh JJ 2021-10-17 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/34680357 ARRDC4 and UBXN1: Novel Target Genes Correlated with Prostate Cancer Gleason Score. High Gleason score in radical prostatectomy 122 cases, 719 controls NA Illumina [242186] 1 Gleason score measurement http://www.ebi.ac.uk/efo/EFO_0007000 GCST90093062 Genome-wide genotyping array 2021-11-18 30842574 Luciano M 2019-03-06 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30842574 The influence of X chromosome variants on trait neuroticism. Neuroticism 405,274 European ancestry individuals NA Illumina [1686693] (imputed) 37 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST012524 Targeted genotyping array [X-chromosome] 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia x sex interaction 31,567 European ancestry cases, 37,494 European ancestry controls, 1,836 East Asian ancestry cases, 3,383 East Asian ancestry controls NA NR [NR] (imputed) 35 schizophrenia, sex interaction measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012311 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia x sex interaction 31,567 European ancestry cases, 37,494 European ancestry controls NA NR [NR] (imputed) 29 schizophrenia, sex interaction measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012310 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia 11,361 European ancestry female cases, 18,119 European ancestry female controls, 20,206 European ancestry male cases, 19,375 European ancestry male controls, 686 East Asian ancestry female cases, 1,907 East Asian ancestry female controls, 1,150 East Asian ancestry male cases, 1,476 East Asian ancestry male controls NA NR [NR] (imputed) 20 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST012309 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia 11,361 European ancestry female cases, 18,119 European ancestry female controls, 20,206 European ancestry male cases, 19,375 European ancestry male controls NA NR [NR] (imputed) 15 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST012308 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Bipolar disorder x sex interaction 19,924 European ancestry cases, 30,547 European ancestry controls NA NR [NR] (imputed) 13 bipolar disorder, sex interaction measurement http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012307 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Bipolar disorder 11,897 European ancestry female cases, 15,538 European ancestry female controls, 8,027 European ancestry male cases, 15,009 European ancestry male controls NA NR [NR] (imputed) 11 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST012306 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Major depressive disorder x sex interaction 15,970 European ancestry cases, 24,984 European ancestry controls NA NR [NR] (imputed) 27 unipolar depression, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012305 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Major depressive disorder 10,865 European ancestry female cases, 12,753 European ancestry female controls, 5,105 European ancestry male cases, 12,231 European ancestry male controls NA NR [NR] (imputed) 6 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST012304 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Recurrent major depressive disorder x sex interaction 5,314 European ancestry cases, 10,149 European ancestry controls NA NR [NR] (imputed) 10 unipolar depression, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012303 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Recurrent major depressive disorder 3,833 European ancestry female cases, 5,280 European ancestry female controls, 1,481 European ancestry male cases, 4,869 European ancestry male controls NA NR [NR] (imputed) 7 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST012302 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or major depressive disorder x sex interaction 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 15,970 European ancestry major depressive disorder cases, 93,025 European ancestry controls NA NR [NR] (imputed) 15 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012301 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or major depressive disorder 11,361 European ancestry schizophrenia female cases, 20,206 European ancestry schizophrenia male cases, 11,897 European ancestry bipolar disorder female cases, 8,027 European ancestry bipolar disorder male cases, 10,865 European ancestry major depressive disorder female cases, 5,105 major depressive disorder male cases, 46,410 European ancestry female controls, 46,615 European ancestry male controls NA NR [NR] (imputed) 8 unipolar depression, bipolar disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST012300 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 15,970 European ancestry major depressive disorder cases, 93,025 European ancestry controls NA NR [NR] (imputed) 22 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012299 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or major depressive disorder x sex interaction 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 15,970 European ancestry major depressive disorder cases, 93,025 European ancestry controls, 1,836 East Asian ancestry schizophrenia cases, 3,383 East Asian ancestry controls NA NR [NR] (imputed) 17 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012298 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or major depressive disorder 11,361 European ancestry schizophrenia female cases, 20,206 European ancestry schizophrenia male cases, 11,897 European ancestry bipolar disorder female cases, 8,027 European ancestry bipolar disorder male cases, 10,865 European ancestry major depressive disorder female cases, 5,105 major depressive disorder male cases, 46,410 European ancestry female controls, 46,615 European ancestry male controls, 686 East Asian ancestry schizophrenia female cases, 1,907 East Asian ancestry female controls, 1,150 East Asian ancestry schizophrenia male cases, 1,476 East Asian ancestry male controls NA NR [NR] (imputed) 13 unipolar depression, bipolar disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST012297 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or major depressive disorder x sex interaction (3df) 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 15,970 European ancestry major depressive disorder cases, 93,025 European ancestry controls, 1,836 East Asian ancestry schizophrenia cases, 3,383 East Asian ancestry controls NA NR [NR] (imputed) 21 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012296 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 5,314 European ancestry recurrent major depressive disorder cases, 78,190 European ancestry controls NA NR [NR] (imputed) 16 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012295 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or recurrent major depressive disorder 11,361 European ancestry schizophrenia female cases, 20,206 European ancestry schizophrenia male cases, 11,897 European ancestry bipolar disorder female cases, 8,027 European ancestry bipolar disorder male cases, 3,833 European ancestry recurrent major depressive disorder female cases, 1,481 recurrent major depressive disorder male cases, 38,937 European ancestry female controls, 29,714 European ancestry male controls NA NR [NR] (imputed) 5 unipolar depression, bipolar disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST012294 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction (3df) 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 5,314 European ancestry recurrent major depressive disorder cases, 78,190 European ancestry controls NA NR [NR] (imputed) 19 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012293 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 5,314 European ancestry recurrent major depressive disorder cases, 78,190 European ancestry controls, 1,836 East Asian ancestry schizophrenia cases, 3,383 East Asian ancestry controls NA NR [NR] (imputed) 14 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012292 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or recurrent major depressive disorder 11,361 European ancestry schizophrenia female cases, 20,206 European ancestry schizophrenia male cases, 11,897 European ancestry bipolar disorder female cases, 8,027 European ancestry bipolar disorder male cases, 3,833 European ancestry recurrent major depressive disorder female cases, 1,481 recurrent major depressive disorder male cases, 38,937 European ancestry female controls, 29,714 European ancestry male controls, 686 East Asian ancestry schizophrenia female cases, 1,907 East Asian ancestry female controls, 1,150 East Asian ancestry schizophrenia male cases, 1,476 East Asian ancestry male controls NA NR [NR] (imputed) 7 unipolar depression, bipolar disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST012291 Genome-wide genotyping array 2021-09-03 34099189 Blokland GAM 2021-03-23 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34099189 Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders. Schizophrenia, bipolar disorder or recurrent major depressive disorder x sex interaction (3df) 31,567 European ancestry schizophrenia cases,19,924 European ancestry bipolar disorder cases, 5,314 European ancestry recurrent major depressive disorder cases, 78,190 European ancestry controls, 1,836 East Asian ancestry schizophrenia cases, 3,383 East Asian ancestry controls NA NR [NR] (imputed) 21 unipolar depression, bipolar disorder, schizophrenia, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0008343 GCST012290 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-P_38:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060367 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-P_40:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060416 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-P_40:6_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060510 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-P(31:1)_[M+H]+/Phosphatidylethanolamine-O(34:2)_[M+H]+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060654 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-P(39:7)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060815 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(30:1)_[M-H]-/Phosphatidylethanolamine(33:1)_[M-H]- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060653 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(32:0)_[M+H]1+/Phosphatidylethanolamine(35:0)_[M+H]1+/Phosphatidate(37:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 72 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060686 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(32:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060791 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(32:1)_[M+H]1+/Phosphatidylethanolamine(35:1)_[M+H]1+/Phosphatidate(37:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060681 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(32:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060785 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(32:2)_[M-H]1-/Phosphatidylethanolamine(35:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060672 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Bile acid(DCA)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 bile acid measurement http://www.ebi.ac.uk/efo/EFO_0020050 GCST90060135 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_40:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90060198 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_41:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90060207 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_42:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060214 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_42:1_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060205 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(32:2)_[M+H]1+/Phosphatidylethanolamine(35:2)_[M+H]1+/Phosphatidate(37:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060675 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(32:2)_[M+OAc]1-/Phosphatidylserine(36:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060778 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(33:1)_[M+H]1+/Phosphatidylethanolamine(36:1)_[M+H]1+/Phosphatidate(38:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060701 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(33:2)_[M+H]1+/Phosphatidylethanolamine(36:2)_[M+H]1+/Phosphatidate(38:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 88 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060696 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(33:3)_[M+H]1+/Phosphatidylethanolamine(36:3)_[M+H]1+/Phosphatidate(38:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 78 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060692 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(33:3)_[M+OAc]1-/Phosphatidylserine(37:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060810 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(33:4)_[M+OAc]-/Phosphatidylserine(37:3)_[M-H]- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060804 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:0)_[M+H]1+/Phosphatidylethanolamine(37:0)_[M+H]1+/Phosphatidate(39:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060730 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:1)_[M+H]1+/Phosphatidylethanolamine(37:1)_[M+H]1+/Phosphatidate(39:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060724 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_36:3_[M+OAc]1-/Phosphatidylcholine-P_36:2_[M+OAc]1-/Phosphatidylserine-O_40:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060437 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_36:4_[M+H]1+/Phosphatidylcholine-P_36:3_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 33 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060318 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_36:4_[M+OAc]1-/Phosphatidylcholine-P_36:3_[M+OAc]1-/Phosphatidylserine-O_40:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060434 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_36:5_[M+OAc]1-/Phosphatidylcholine-P_36:4_[M+OAc]1-/Phosphatidylserine-O_40:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060429 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_37:1_[M+H]1+/Phosphatidylcholine-P_37:0_[M+H]1+/Phosphatidylethanolamine-O_40:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060361 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_37:2_[M+H]1+/Phosphatidylcholine-P_37:1_[M+H]1+/Phosphatidylethanolamine-O_40:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060355 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_38:1_[M+H]1+/Phosphatidylcholine-P_38:0_[M+H]1+/Phosphatidylethanolamine-P_41:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060390 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_38:2_[M+H]1+/Phosphatidylcholine-P_38:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060385 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_38:4_[M+H]1+/Phosphatidylcholine-P_38:3_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060379 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_38:4_[M+OAc]1-/Phosphatidylcholine-P_38:3_[M+OAc]1-/Phosphatidylserine-P_42:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060486 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_38:5_[M+H]1+/Phosphatidylcholine-P_38:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 28 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060375 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_38:5_[M+OAc]1-/Phosphatidylcholine-P_38:4_[M+OAc]1-/Phosphatidylserine-O_42:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060483 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_38:6_[M+OAc]1-/Phosphatidylcholine-P_38:5_[M+OAc]1-/Phosphatidylserine-P_42:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060476 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_39:0_[M+H]1+/Phosphatidylethanolamine-O_42:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060417 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_40:5_[M+H]1+/Phosphatidylcholine-P_40:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060423 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_40:6_[M+H]1+/Phosphatidylcholine-P_40:5_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060420 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_40:6_[M+OAc]1-/Phosphatidylcholine-P_40:5_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060513 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_42:6_[M+OAc]1-/Phosphatidylcholine-P_42:5_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 21 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060545 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_44:5_[M+H]1+/Phosphatidylcholine-P_44:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060514 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_44:5_[M+OAc]1-/Phosphatidylcholine-P_44:4_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 28 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060557 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(32:0)_[M+H]1+/Phosphatidylethanolamine-O(35:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 16 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060671 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(33:1)_[M+H]1+/Phosphatidylcholine-P(33:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060682 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(33:2)_[M+H]1+/Phosphatidylcholine-P(33:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060677 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(34:1)_[M+H]1+/Phosphatidylcholine-P(34:0)_[M+H]1+/Phosphatidylethanolamine-O(37:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 14 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060703 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_36:3_[M+H]1+/Phosphatidylcholine-P_36:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060321 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(42:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060659 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(44:11)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060667 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesterol_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 sterol measurement http://www.ebi.ac.uk/efo/EFO_0010231 GCST90060133 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesterol_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 43 sterol measurement http://www.ebi.ac.uk/efo/EFO_0010231 GCST90060591 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_14:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 10 cholesteryl ester 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010340 GCST90060197 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_15:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90060202 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_16:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 22 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90060211 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_16:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90060210 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_17:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90060217 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_17:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90060216 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_18:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 10 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90060222 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_18:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90060221 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_18:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 20 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90060220 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_18:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 34 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90060218 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_20:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 41 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90060231 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_20:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 39 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90060228 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_22:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 13 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90060251 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester_22:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 27 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90060248 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(14:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 2 cholesteryl ester 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010340 GCST90060616 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(16:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 68 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90060627 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(16:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 20 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90060626 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(17:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 19 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90060631 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(18:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 47 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90060637 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(18:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 45 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90060636 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(18:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 21 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90060635 Genome-wide genotyping array 2021-10-26 34441435 Corma-Gomez A 2021-08-20 Diagnostics (Basel) www.ncbi.nlm.nih.gov/pubmed/34441435 A Genome-Wide Association Study on Liver Stiffness Changes during Hepatitis C Virus Infection Cure. Liver stiffness changes at sustained virological response following antiviral therapy in HCV infection 242 European ancestry individuals NA Affymetrix [6939676] (imputed) 13 response to antiviral drug, cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0010123, http://www.ebi.ac.uk/efo/EFO_0001422 GCST90032157 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V18: Pedal cycle rider injured in noncollision transport accident (Gene-based burden) 1,465 European ancestry cases, 386,440 European ancestry controls NA Illumina [185343] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085080 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M62: Muscle or soft tissue problem 3,372 European ancestry cases, 325,680 European ancestry controls NA Affymetrix, Illumina [456275] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90077776 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V18.4: Pedal cycle driver injured in noncollision transport accident in traffic accident (Gene-based burden) 591 European ancestry cases, 387,339 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085079 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33: nasal polyps 1,790 European ancestry cases, 327,262 European ancestry controls NA Affymetrix, Illumina [456275] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90077839 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V43: Car occupant injured in collision with car, pick-up truck or van (Gene-based burden) 726 European ancestry cases, 387,204 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085082 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34: nasal sinus disorder 1,548 European ancestry cases, 327,504 European ancestry controls NA Affymetrix, Illumina [456275] 0 paranasal sinus disease http://www.ebi.ac.uk/efo/EFO_0009481 GCST90077833 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V43.5: Car driver injured in collision with car, pick-up truck or van in traffic accident (Gene-based burden) 520 European ancestry cases, 387,410 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085081 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F430: nervous breakdown 637 European ancestry cases, 328,415 European ancestry controls NA Affymetrix, Illumina [456275] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90077766 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V89: Motor- or nonmotor-vehicle accident, type of vehicle unspecified (Gene-based burden) 1,541 European ancestry cases, 378,330 European ancestry controls NA Illumina [185229] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085084 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K20: oesophagitis barretts oesophagus 1,386 European ancestry cases, 327,666 European ancestry controls NA Affymetrix, Illumina [456275] 0 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90077695 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V89.2: Person injured in unspecified motor-vehicle accident, traffic (Gene-based burden) 1,485 European ancestry cases, 378,407 European ancestry controls NA Illumina [185229] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085083 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19: osteoarthritis 33,708 European ancestry cases, 295,344 European ancestry controls NA Affymetrix, Illumina [456275] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90077876 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W00: Fall due to ice and snow (Gene-based burden) 1,315 European ancestry cases, 386,539 European ancestry controls NA Illumina [185343] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085086 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81: osteoporosis 6,633 European ancestry cases, 322,419 European ancestry controls NA Affymetrix, Illumina [456275] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90077780 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W00.9: Unspecified fall due to ice and snow (Gene-based burden) 617 European ancestry cases, 387,313 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085085 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: other joint disorder 2,283 European ancestry cases, 326,769 European ancestry controls NA Affymetrix, Illumina [456275] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90077880 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01: Fall on same level from slipping, tripping and stumbling (Gene-based burden) 7,826 European ancestry cases, 379,915 European ancestry controls NA Illumina [185341] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085091 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G98: other neurological problem 1,701 European ancestry cases, 327,351 European ancestry controls NA Affymetrix, Illumina [456275] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90077843 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.0: Fall on same level from slipping, tripping and stumbling without subsequent striking against object (Gene-based burden) 2,287 European ancestry cases, 385,443 European ancestry controls NA Illumina [185341] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085087 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28: Other renal or kidney problem 1,807 European ancestry cases, 327,245 European ancestry controls NA Affymetrix, Illumina [456275] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90077825 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.4: Street and highway (Gene-based burden) 1,708 European ancestry cases, 386,222 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085088 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98: other respiratory problems 685 European ancestry cases, 328,367 European ancestry controls NA Affymetrix, Illumina [456275] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90077680 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.8: Other specified place (Gene-based burden) 998 European ancestry cases, 386,932 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085089 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K85: pancreatitis 868 European ancestry cases, 328,184 European ancestry controls NA Affymetrix, Illumina [456275] 0 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90077707 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.9: Unspecified place (Gene-based burden) 2,111 European ancestry cases, 385,819 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085090 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59: constipation 500 European ancestry cases, 328,552 European ancestry controls NA Affymetrix, Illumina [456275] 0 Constipation http://purl.obolibrary.org/obo/HP_0002019 GCST90077958 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S83.2: Tear of meniscus, current injury (Gene-based burden) 813 European ancestry cases, 384,622 European ancestry controls NA Illumina [185313] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085016 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50: crohns disease 1,250 European ancestry cases, 327,802 European ancestry controls NA Affymetrix, Illumina [456275] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90077870 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S86: Injury of muscle, fascia and tendon at lower leg level (Gene-based burden) 1,044 European ancestry cases, 385,884 European ancestry controls NA Illumina [185331] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085019 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30: Cystitis 546 European ancestry cases, 328,506 European ancestry controls NA Affymetrix, Illumina [456275] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90077915 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S86.0: Injury of Achilles tendon (Gene-based burden) 825 European ancestry cases, 386,304 European ancestry controls NA Illumina [185331] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085018 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I80: deep venous thrombosis 8,088 European ancestry cases, 320,964 European ancestry controls NA Affymetrix, Illumina [456275] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90077670 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S89: Other and unspecified injuries of lower leg (Gene-based burden) 1,229 European ancestry cases, 381,176 European ancestry controls NA Illumina [185231] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085022 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F32: depression 23,026 European ancestry cases, 306,026 European ancestry controls NA Affymetrix, Illumina [456275] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90077762 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S89.9: Unspecified injury of lower leg (Gene-based burden) 1,155 European ancestry cases, 381,371 European ancestry controls NA Illumina [185237] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085021 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E14: diabetes 16,961 European ancestry cases, 312,091 European ancestry controls NA Affymetrix, Illumina [456275] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90077723 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S89.90: Unspecified injury of unspecified lower leg (Gene-based burden) 915 European ancestry cases, 381,599 European ancestry controls NA Illumina [185237] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085020 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H36: diabetic eye disease 970 European ancestry cases, 328,082 European ancestry controls NA Affymetrix, Illumina [456275] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90077753 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S92: Fracture of foot and toe, except ankle (Gene-based burden) 1,806 European ancestry cases, 380,162 European ancestry controls NA Illumina [185237] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90085025 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51: disc degeneration 938 European ancestry cases, 328,114 European ancestry controls NA Affymetrix, Illumina [456275] 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST90077922 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S92.3: Fracture of metatarsal bone(s) (Gene-based burden) 710 European ancestry cases, 384,817 European ancestry controls NA Illumina [185306] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90085024 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57: diverticular disease diverticulitis 4,946 European ancestry cases, 324,106 European ancestry controls NA Affymetrix, Illumina [456275] 0 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90077864 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S92.30: Fracture of unspecified metatarsal bone(s) (Gene-based burden) 635 European ancestry cases, 385,120 European ancestry controls NA Illumina [185313] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90085023 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04: dry eyes 874 European ancestry cases, 328,178 European ancestry controls NA Affymetrix, Illumina [456275] 0 dry eye syndrome http://www.ebi.ac.uk/efo/EFO_1000906 GCST90077919 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93: Dislocation and sprain of joints and ligaments at ankle, foot and toe level (Gene-based burden) 1,344 European ancestry cases, 379,230 European ancestry controls NA Illumina [185237] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085029 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K26: Duodenal ulcer 1,573 European ancestry cases, 327,479 European ancestry controls NA Affymetrix, Illumina [456275] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90077862 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93.4: Sprain of ankle (Gene-based burden) 1,060 European ancestry cases, 380,874 European ancestry controls NA Illumina [185253] 0 sprain http://www.ebi.ac.uk/efo/EFO_0009582 GCST90085028 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R12: dyspepsia indigestion 792 European ancestry cases, 328,260 European ancestry controls NA Affymetrix, Illumina [456275] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90077910 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93.40: Sprain of unspecified ligament of ankle (Gene-based burden) 900 European ancestry cases, 381,230 European ancestry controls NA Illumina [185258] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085027 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81: ear vestibular disorder 3,505 European ancestry cases, 325,547 European ancestry controls NA Affymetrix, Illumina [456275] 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90077835 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R17: jaundice unknown cause 557 European ancestry cases, 328,495 European ancestry controls NA Affymetrix, Illumina [456275] 0 Jaundice http://purl.obolibrary.org/obo/HP_0000952 GCST90077908 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.5: Infection and inflammatory reaction due to internal joint prosthesis (Gene-based burden) 652 European ancestry cases, 387,277 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085066 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: joint disorder 1,757 European ancestry cases, 327,295 European ancestry controls NA Affymetrix, Illumina [456275] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90077774 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.8: Other specified complications of internal orthopedic prosthetic devices, implants and grafts (Gene-based burden) 6,289 European ancestry cases, 373,482 European ancestry controls NA Illumina [185200] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085068 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: joint pain 1,766 European ancestry cases, 327,286 European ancestry controls NA Affymetrix, Illumina [456275] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90077926 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.84: Pain due to internal orthopedic prosthetic devices, implants and grafts (Gene-based burden) 4,278 European ancestry cases, 375,391 European ancestry controls NA Illumina [185196] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085067 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20: kidney stone ureter stone bladder stone 3,296 European ancestry cases, 325,756 European ancestry controls NA Affymetrix, Illumina [456275] 0 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90077713 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85: Complications of other internal prosthetic devices, implants and grafts (Gene-based burden) 2,918 European ancestry cases, 384,896 European ancestry controls NA Illumina [185343] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085073 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K87: Liver, biliary or pancreas problem 753 European ancestry cases, 328,299 European ancestry controls NA Affymetrix, Illumina [456275] 0 biliary tract disease, pancreas disease, liver disease http://www.ebi.ac.uk/efo/EFO_0009534, http://www.ebi.ac.uk/efo/EFO_0009605, http://www.ebi.ac.uk/efo/EFO_0001421 GCST90077690 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85.5: Mechanical complication of gastrointestinal prosthetic devices, implants and grafts (Gene-based burden) 519 European ancestry cases, 387,408 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085070 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K90: malabsorption coeliac disease 1,766 European ancestry cases, 327,286 European ancestry controls NA Affymetrix, Illumina [456275] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90077860 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85.7: Infection and inflammatory reaction due to other internal prosthetic devices, implants and grafts (Gene-based burden) 680 European ancestry cases, 387,244 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085071 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B05: measles morbillivirus 5,294 European ancestry cases, 323,758 European ancestry controls NA Affymetrix, Illumina [456275] 0 measles http://www.ebi.ac.uk/efo/EFO_1002025 GCST90077942 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85.8: Other specified complications of internal prosthetic devices, implants and grafts, not elsewhere classified (Gene-based burden) 589 European ancestry cases, 387,341 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085072 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81: menieres disease 1,091 European ancestry cases, 327,961 European ancestry controls NA Affymetrix, Illumina [456275] 0 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90077841 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T88: Other complications of surgical and medical care, not elsewhere classified (Gene-based burden) 976 European ancestry cases, 386,677 European ancestry controls NA Illumina [185334] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085074 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G03: meningitis 1,689 European ancestry cases, 327,363 European ancestry controls NA Affymetrix, Illumina [456275] 0 infectious meningitis http://www.ebi.ac.uk/efo/EFO_0000584 GCST90077735 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T90: Sequelae of injuries of head (Gene-based burden) 649 European ancestry cases, 387,281 European ancestry controls NA Illumina [185342] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90085075 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G43: Migraine 11,475 European ancestry cases, 317,577 European ancestry controls NA Affymetrix, Illumina [456275] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90077746 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T92: Sequelae of injuries of upper limb (Gene-based burden) 835 European ancestry cases, 387,095 European ancestry controls NA Illumina [185344] 0 limb injury http://www.ebi.ac.uk/efo/EFO_0009509 GCST90085076 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G35: Multiple sclerosis 1,463 European ancestry cases, 327,589 European ancestry controls NA Affymetrix, Illumina [456275] 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90077740 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T93: Sequelae of injuries of lower limb (Gene-based burden) 975 European ancestry cases, 386,955 European ancestry controls NA Illumina [185344] 0 limb injury http://www.ebi.ac.uk/efo/EFO_0009509 GCST90085077 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B26: mumps epidemic parotitis 3,260 European ancestry cases, 325,792 European ancestry controls NA Affymetrix, Illumina [456275] 0 Mumps virus infectious disease http://www.ebi.ac.uk/efo/EFO_0007383 GCST90077944 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 U80: Agent resistant to penicillin and related antibiotics (Gene-based burden) 876 European ancestry cases, 387,054 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085078 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 no: muscle or soft tissue injuries 3,750 European ancestry cases, 325,302 European ancestry controls NA Affymetrix, Illumina [456275] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90077827 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82: Fracture of lower leg, including ankle (Gene-based burden) 7,211 European ancestry cases, 374,121 European ancestry controls NA Illumina [185281] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085015 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L13: blistering desquamating skin disorder 653 European ancestry cases, 328,399 European ancestry controls NA Affymetrix, Illumina [456275] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90077858 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.1: Fracture of upper end of tibia (Gene-based burden) 762 European ancestry cases, 387,022 European ancestry controls NA Illumina [185342] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085005 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M85: bone disorder 841 European ancestry cases, 328,211 European ancestry controls 1,976 European ancestry cases, 115,394 European ancestry controls Affymetrix, Illumina [456275] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90077770 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.10: Unspecified fracture of upper end of tibia (Gene-based burden) 612 European ancestry cases, 387,202 European ancestry controls NA Illumina [185341] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085004 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J47: Bronchiectasis 1,030 European ancestry cases, 328,022 European ancestry controls NA Affymetrix, Illumina [456275] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90077678 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.2: Fracture of shaft of tibia (Gene-based burden) 684 European ancestry cases, 386,536 European ancestry controls NA Illumina [185334] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90085006 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J40: bronchitis 3,397 European ancestry cases, 325,655 European ancestry controls NA Affymetrix, Illumina [456275] 0 bronchial disease http://www.ebi.ac.uk/efo/EFO_1002018 GCST90077831 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.3: Fracture of lower end of tibia (Gene-based burden) 648 European ancestry cases, 387,110 European ancestry controls NA Illumina [185343] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90085007 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56: carpal tunnel syndrome 830 European ancestry cases, 328,222 European ancestry controls NA Affymetrix, Illumina [456275] 0 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90077930 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.4: Fracture of shaft of fibula (Gene-based burden) 524 European ancestry cases, 386,685 European ancestry controls NA Illumina [185340] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085008 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26: cataract 7,792 European ancestry cases, 321,260 European ancestry controls NA Affymetrix, Illumina [456275] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90077757 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.6: Fracture of lateral malleolus (Gene-based burden) 1,103 European ancestry cases, 385,515 European ancestry controls NA Illumina [185323] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085010 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47: cervical spondylosis 2,805 European ancestry cases, 326,247 European ancestry controls NA Affymetrix, Illumina [456275] 0 cervical spondylosis http://www.ebi.ac.uk/efo/EFO_0009610 GCST90077892 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.60: Fracture of lateral malleolus (Gene-based burden) 832 European ancestry cases, 387,098 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085009 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B01: chickenpox 6,575 European ancestry cases, 322,477 European ancestry controls NA Affymetrix, Illumina [456275] 0 chickenpox http://www.ebi.ac.uk/efo/EFO_0007204 GCST90077948 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.8: Other fractures of lower leg (Gene-based burden) 2,701 European ancestry cases, 384,726 European ancestry controls NA Illumina [185340] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085012 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80: cholelithiasis or gall stones 7,073 European ancestry cases, 321,979 European ancestry controls NA Affymetrix, Illumina [456275] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90077705 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.80: Other fractures of lower leg (Gene-based burden) 2,182 European ancestry cases, 385,748 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085011 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44: chronic obstructive airways disease copd 1,651 European ancestry cases, 327,401 European ancestry controls NA Affymetrix, Illumina [456275] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90077674 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.9: Unspecified fracture of lower leg (Gene-based burden) 701 European ancestry cases, 383,185 European ancestry controls NA Illumina [185301] 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90085014 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32: Chronic sinusitis 2,961 European ancestry cases, 326,091 European ancestry controls NA Affymetrix, Illumina [456275] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90077837 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.90: Unspecified fracture of unspecified lower leg (Gene-based burden) 684 European ancestry cases, 383,198 European ancestry controls NA Illumina [185301] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085013 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52: colitis not crohns or ulcerative colitis 1,104 European ancestry cases, 327,948 European ancestry controls NA Affymetrix, Illumina [456275] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90077866 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S83: Dislocation and sprain of joints and ligaments of knee (Gene-based burden) 1,620 European ancestry cases, 379,952 European ancestry controls NA Illumina [185264] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90085017 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.0: Haemorrhage and haematoma complicating a procedure, not elsewhere classified (T81.0) (Gene-based burden) 6,401 European ancestry cases, 381,515 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085054 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R01: heart valve problem or heart murmur 2,752 European ancestry cases, 326,300 European ancestry controls NA Affymetrix, Illumina [456275] 0 Abnormal cardiovascular system physiology http://purl.obolibrary.org/obo/HP_0011025 GCST90077662 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.149.88: Postprocedural shock (Gene-based burden) 16,135 European ancestry cases, 368,843 European ancestry controls NA Illumina [185305] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085055 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B98: helicobacter pylori 1,318 European ancestry cases, 327,734 European ancestry controls NA Affymetrix, Illumina [456275] 0 Helicobacter pylori http://purl.obolibrary.org/obo/NCBITaxon_210 GCST90077850 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.2: Accidental puncture and laceration during a procedure, not elsewhere classified (T81.2) (Gene-based burden) 1,820 European ancestry cases, 386,110 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085056 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K44: hiatus hernia 9,911 European ancestry cases, 319,141 European ancestry controls NA Affymetrix, Illumina [456275] 0 Hiatus hernia http://purl.obolibrary.org/obo/HP_0002036 GCST90077886 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.3: Disruption of wound, not elsewhere classified (Gene-based burden) 1,668 European ancestry cases, 386,164 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085057 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78: high cholesterol 49,060 European ancestry cases, 279,992 European ancestry controls NA Affymetrix, Illumina [456275] 2 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90077884 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.4: Infection following a procedure (Gene-based burden) 5,665 European ancestry cases, 379,815 European ancestry controls NA Illumina [185306] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085058 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05: Hyperthyroidism or thyrotoxicosis 2,796 European ancestry cases, 326,256 European ancestry controls NA Affymetrix, Illumina [456275] 0 hyperthyroidism, Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009189, http://www.ebi.ac.uk/efo/EFO_0009190 GCST90077729 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.815.013.: Other complications of procedures, not elsewhere classified (Gene-based burden) 2,476 European ancestry cases, 385,251 European ancestry controls NA Illumina [185342] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085059 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E03: Hypothyroidism or myxoedema 18,362 European ancestry cases, 310,690 European ancestry controls NA Affymetrix, Illumina [456275] 0 myxedema, hypothyroidism http://www.ebi.ac.uk/efo/EFO_1001055, http://www.ebi.ac.uk/efo/EFO_0004705 GCST90077731 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T82: Complications of cardiac and vascular prosthetic devices, implants and grafts (Gene-based burden) 3,110 European ancestry cases, 384,779 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085061 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B27: infectious mononucleosis glandular fever epstein barr virus ebv 836 European ancestry cases, 328,216 European ancestry controls NA Affymetrix, Illumina [456275] 0 infectious mononucleosis http://www.ebi.ac.uk/efo/EFO_0007326 GCST90077940 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T82.7: Infection and inflammatory reaction due to other cardiac and vascular devices, implants and grafts (Gene-based burden) 1,068 European ancestry cases, 386,860 European ancestry controls NA Illumina [185340] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085060 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B19: infective viral hepatitis 861 European ancestry cases, 328,191 European ancestry controls NA Affymetrix, Illumina [456275] 0 viral human hepatitis infection http://www.ebi.ac.uk/efo/EFO_0004196 GCST90077703 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T83: Complications of genitourinary prosthetic devices, implants and grafts (Gene-based burden) 1,621 European ancestry cases, 386,046 European ancestry controls NA Illumina [185341] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085063 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40: Inguinal hernia 2,212 European ancestry cases, 326,840 European ancestry controls NA Affymetrix, Illumina [456275] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90077913 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T83.0: Mechanical complication of urinary catheter (Gene-based burden) 575 European ancestry cases, 387,352 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085062 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50: iron deficiency anaemia 2,361 European ancestry cases, 326,691 European ancestry controls NA Affymetrix, Illumina [456275] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90077788 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84: Complications of internal orthopedic prosthetic devices, implants and grafts (Gene-based burden) 10,104 European ancestry cases, 369,829 European ancestry controls NA Illumina [185203] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085069 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49: irregular heart beat 943 European ancestry cases, 328,109 European ancestry controls NA Affymetrix, Illumina [456275] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90077898 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.0: Mechanical complication of internal joint prosthesis (Gene-based burden) 2,223 European ancestry cases, 385,699 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085064 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58: Irritable bowel syndrome 9,503 European ancestry cases, 319,549 European ancestry controls NA Affymetrix, Illumina [456275] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90077700 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.1: Mechanical complication of internal fixation device of bones of limb (Gene-based burden) 1,002 European ancestry cases, 386,928 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085065 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S8220: fracture tibia 597 European ancestry cases, 328,455 European ancestry controls NA Affymetrix, Illumina [456275] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90077981 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T43.2: Poisoning by, adverse effect of and underdosing of other and unspecified antidepressants (Gene-based burden) 774 European ancestry cases, 387,027 European ancestry controls NA Illumina [185340] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085041 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42: fracture upper arm humerus elbow 1,059 European ancestry cases, 327,993 European ancestry controls NA Affymetrix, Illumina [456275] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90077969 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T46: Poisoning by, adverse effect of and underdosing of agents primarily affecting the cardiovascular system (Gene-based burden) 621 European ancestry cases, 384,441 European ancestry controls NA Illumina [185309] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085043 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62: fracture wrist colles fracture 1,406 European ancestry cases, 327,646 European ancestry controls NA Affymetrix, Illumina [456275] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90077973 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50: Poisoning by, adverse effect of and underdosing of diuretics and other and unspecified drugs, medicaments and biological substances (Gene-based burden) 1,778 European ancestry cases, 379,361 European ancestry controls NA Illumina [185237] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085047 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K25: gastric stomach ulcers 3,114 European ancestry cases, 325,938 European ancestry controls NA Affymetrix, Illumina [456275] 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90077696 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50.9: Poisoning by, adverse effect of and underdosing of other and unspecified drugs, medicaments and biological substances (Gene-based burden) 1,659 European ancestry cases, 380,109 European ancestry controls NA Illumina [185241] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085046 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29: gastritis gastric erosions 788 European ancestry cases, 328,264 European ancestry controls NA Affymetrix, Illumina [456275] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90077698 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50.90: Poisoning by, adverse effect of and underdosing of unspecified drugs, medicaments and biological substances (Gene-based burden) 1,366 European ancestry cases, 380,369 European ancestry controls NA Illumina [185241] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085045 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40: Glaucoma 4,377 European ancestry cases, 324,675 European ancestry controls NA Affymetrix, Illumina [456275] 1 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90077755 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50.905.: Adverse effect of unspecified drugs, medicaments and biological substances (Gene-based burden) 682 European ancestry cases, 383,434 European ancestry controls NA Illumina [185274] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085044 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10: Gout 5,396 European ancestry cases, 323,656 European ancestry controls NA Affymetrix, Illumina [456275] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90077878 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T51: Toxic effect of alcohol (Gene-based burden) 1,105 European ancestry cases, 386,807 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085049 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64: haemorrhoids piles 1,291 European ancestry cases, 327,761 European ancestry controls NA Affymetrix, Illumina [456275] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90077906 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T51.0: Toxic effect of ethanol (Gene-based burden) 952 European ancestry cases, 386,976 European ancestry controls NA Illumina [185344] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085048 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30: hayfever allergic rhinitis 21,078 European ancestry cases, 307,974 European ancestry controls NA Affymetrix, Illumina [456275] 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90077816 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78: Adverse effects, not elsewhere classified (Gene-based burden) 2,437 European ancestry cases, 377,187 European ancestry controls NA Illumina [185210] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085052 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R51: headaches (not migraine) 3,285 European ancestry cases, 325,767 European ancestry controls NA Affymetrix, Illumina [456275] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90077845 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78.4: Other and unspecified allergy (Gene-based burden) 1,497 European ancestry cases, 379,554 European ancestry controls NA Illumina [185232] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085051 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49: heart arrhythmia 2,296 European ancestry cases, 326,756 European ancestry controls NA Affymetrix, Illumina [456275] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90077660 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78.40: Allergy, unspecified (Gene-based burden) 1,044 European ancestry cases, 379,975 European ancestry controls NA Illumina [185232] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085050 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21: heart attack myocardial infarction 9,479 European ancestry cases, 319,573 European ancestry controls NA Affymetrix, Illumina [456275] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90077658 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T79: Certain early complications of trauma, not elsewhere classified (Gene-based burden) 625 European ancestry cases, 387,014 European ancestry controls NA Illumina [185342] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90085053 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I52: heart cardiac problem 1,442 European ancestry cases, 327,610 European ancestry controls NA Affymetrix, Illumina [456275] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90077648 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93.409.: Sprain of unspecified ligament of unspecified ankle (Gene-based burden) 899 European ancestry cases, 381,231 European ancestry controls NA Illumina [185245] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085026 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L30: Eczema or dermatitis 10,233 European ancestry cases, 318,819 European ancestry controls NA Affymetrix, Illumina [456275] 1 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90077854 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S99: Other and unspecified injuries of ankle and foot (Gene-based burden) 737 European ancestry cases, 382,054 European ancestry controls NA Illumina [185211] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085031 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J43: emphysema chronic bronchitis 5,961 European ancestry cases, 323,091 European ancestry controls NA Affymetrix, Illumina [456275] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90077676 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S99.9: Unspecified injury of ankle and foot (Gene-based burden) 699 European ancestry cases, 382,202 European ancestry controls NA Illumina [185213] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085030 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40: epilepsy 3,248 European ancestry cases, 325,804 European ancestry controls NA Affymetrix, Illumina [456275] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90077744 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T14: Injury of unspecified body region (Gene-based burden) 4,277 European ancestry cases, 364,018 European ancestry controls NA Illumina [185027] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085033 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I10: essential hypertension 2,588 European ancestry cases, 326,464 European ancestry controls NA Affymetrix, Illumina [456275] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90077652 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T14.8: Other injury of unspecified body region (Gene-based burden) 3,537 European ancestry cases, 368,536 European ancestry controls NA Illumina [185080] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085032 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H029: Eye or eyelid problem 3,320 European ancestry cases, 325,732 European ancestry controls NA Affymetrix, Illumina [456275] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90077733 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T39: Poisoning by, adverse effect of and underdosing of nonopioid analgesics, antipyretics and antirheumatics (Gene-based burden) 2,026 European ancestry cases, 384,627 European ancestry controls NA Illumina [185323] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085036 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79: fibromyalgia 766 European ancestry cases, 328,286 European ancestry controls NA Affymetrix, Illumina [456275] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90077932 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T39.1: Poisoning by, adverse effect of and underdosing of 4-Aminophenol derivatives (Gene-based burden) 1,576 European ancestry cases, 386,288 European ancestry controls NA Illumina [185344] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085034 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42: fracture clavicle collar bone 576 European ancestry cases, 328,476 European ancestry controls NA Affymetrix, Illumina [456275] 0 clavicle fracture http://www.ebi.ac.uk/efo/EFO_0009614 GCST90077967 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T39.3: Poisoning by, adverse effect of and underdosing of other nonsteroidal anti-inflammatory drugs [NSAID] (Gene-based burden) 517 European ancestry cases, 386,541 European ancestry controls NA Illumina [185335] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085035 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S824: fracture fibula 574 European ancestry cases, 328,478 European ancestry controls NA Affymetrix, Illumina [456275] 0 fibula fracture http://www.ebi.ac.uk/efo/EFO_0009613 GCST90077983 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T40: Poisoning by, adverse effect of and underdosing of narcotics and psychodysleptics [hallucinogens] (Gene-based burden) 860 European ancestry cases, 386,651 European ancestry controls NA Illumina [185339] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085038 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S6260: fracture finger 683 European ancestry cases, 328,369 European ancestry controls NA Affymetrix, Illumina [456275] 0 finger fracture http://www.ebi.ac.uk/efo/EFO_0009616 GCST90077975 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T40.2: Poisoning by, adverse effect of and underdosing of other opioids (Gene-based burden) 636 European ancestry cases, 387,063 European ancestry controls NA Illumina [185340] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085037 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52: Fracture of forearm or wrist 997 European ancestry cases, 328,055 European ancestry controls NA Affymetrix, Illumina [456275] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90077971 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T42: Poisoning by, adverse effect of and underdosing of antiepileptic, sedative- hypnotic and antiparkinsonism drugs (Gene-based burden) 1,043 European ancestry cases, 386,755 European ancestry controls NA Illumina [185342] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085040 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82: fracture lower leg ankle 1,803 European ancestry cases, 327,249 European ancestry controls NA Affymetrix, Illumina [456275] 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90077979 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T42.4: Poisoning by, adverse effect of and underdosing of benzodiazepines (Gene-based burden) 643 European ancestry cases, 387,246 European ancestry controls NA Illumina [185344] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085039 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S022: fracture nose 626 European ancestry cases, 328,426 European ancestry controls NA Affymetrix, Illumina [456275] 0 nose injury http://www.ebi.ac.uk/efo/EFO_0009623 GCST90077965 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T43: Poisoning by, adverse effect of and underdosing of psychotropic drugs, not elsewhere classified (Gene-based burden) 1,325 European ancestry cases, 386,321 European ancestry controls NA Illumina [185338] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90085042 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteoarthritis (Gene-based burden) 39,005 European ancestry cases, 292,749 European ancestry controls NA Illumina [184201] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90081861 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sensitive stomach (UKB data field 21064) 32,677 European ancestry cases, 109,193 European ancestry controls NA Affymetrix, Illumina [244358] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90078828 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19: osteoarthritis (Gene-based burden) 33,708 European ancestry cases, 295,344 European ancestry controls NA Illumina [184145] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90081862 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma (UKB data field 6152) 50,805 European ancestry cases, 90,156 European ancestry controls NA Affymetrix, Illumina [243196] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90079456 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteomyelitis (Gene-based burden) 688 European ancestry cases, 331,066 European ancestry controls NA Illumina [184201] 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90081763 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood clot in the lung (UKB data field 6152) 3,718 European ancestry cases, 137,243 European ancestry controls NA Affymetrix, Illumina [243196] 0 Abnormal thrombosis http://purl.obolibrary.org/obo/HP_0001977 GCST90079455 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M86: Osteomyelitis (Gene-based burden) 563 European ancestry cases, 328,488 European ancestry controls NA Illumina [184145] 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90081764 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease (UKB data field 6152) 7,705 European ancestry cases, 133,256 European ancestry controls NA Affymetrix, Illumina [243196] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90079454 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteopenia (Gene-based burden) 1,605 European ancestry cases, 330,149 European ancestry controls NA Illumina [184201] 0 Osteopenia http://purl.obolibrary.org/obo/HP_0000938 GCST90081947 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hayfever, allergic rhinitis or eczema (UKB data field 6152) 101,576 European ancestry cases, 39,385 European ancestry controls NA Affymetrix, Illumina [243196] 0 seasonal allergic rhinitis, Eczema http://www.ebi.ac.uk/efo/EFO_0003956, http://purl.obolibrary.org/obo/HP_0000964 GCST90079457 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rino clenil nasal spray 901 European ancestry cases, 319,857 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078228 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.1: Family history of malignant neoplasm of trachea, bronchus and lung (Gene-based burden) 551 European ancestry cases, 386,553 European ancestry controls NA Illumina [185329] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90085316 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - risedronate sodium 928 European ancestry cases, 319,830 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078207 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.3: Family history of malignant neoplasm of breast (Gene-based burden) 2,022 European ancestry cases, 384,012 European ancestry controls NA Illumina [185325] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90085317 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rosiglitazone 601 European ancestry cases, 320,157 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078212 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.4: Family history of malignant neoplasm of genital organs (Gene-based burden) 1,416 European ancestry cases, 385,868 European ancestry controls NA Illumina [185330] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90085318 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rosuvastatin 2,905 European ancestry cases, 317,853 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078225 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.9: Family history of malignant neoplasm, unspecified (Gene-based burden) 740 European ancestry cases, 382,058 European ancestry controls NA Illumina [185253] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90085319 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salamol inhaler 1,374 European ancestry cases, 319,384 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078011 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82: Family history of certain disabilities and chronic diseases (leading to disablement) (Gene-based burden) 48,407 European ancestry cases, 284,122 European ancestry controls NA Illumina [184331] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085325 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salbutamol 5,488 European ancestry cases, 315,270 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078101 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.3: Family history of stroke (Gene-based burden) 7,178 European ancestry cases, 362,654 European ancestry controls NA Illumina [185040] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085321 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salbutamol spacehaler 2,981 European ancestry cases, 317,777 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078167 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.4: Family history of ischemic heart disease and other diseases of the circulatory system (Gene-based burden) 43,852 European ancestry cases, 296,393 European ancestry controls NA Illumina [184491] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085323 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salbutamol product 692 European ancestry cases, 320,066 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078189 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N40: enlarged prostate 6,347 European ancestry cases, 144,811 European ancestry controls NA Affymetrix, Illumina [256146] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90077818 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Muscle or soft tissue injuries (Gene-based burden) 3,750 European ancestry cases, 328,004 European ancestry controls NA Illumina [184201] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081812 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N42: prostate problem (not cancer) 730 European ancestry cases, 150,428 European ancestry controls NA Affymetrix, Illumina [256146] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90077719 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 no: muscle or soft tissue injuries (Gene-based burden) 3,750 European ancestry cases, 325,302 European ancestry controls NA Illumina [184145] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081813 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50: testicular problems (not cancer) 518 European ancestry cases, 150,640 European ancestry controls NA Affymetrix, Illumina [256146] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90077721 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Muscle or soft tissue problem (Gene-based burden) 3,644 European ancestry cases, 328,110 European ancestry controls NA Illumina [184201] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90081761 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severe obesity 7,973 European ancestry cases, 142,553 European ancestry controls NA Affymetrix, Illumina [255850] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90081528 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M62: Muscle or soft tissue problem (Gene-based burden) 3,372 European ancestry cases, 325,680 European ancestry controls NA Illumina [184145] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90081762 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Born by caesarian section (UKB data field 21066) 3,960 European ancestry cases, 142,538 European ancestry controls NA Affymetrix, Illumina [250882] 0 cesarean section http://www.ebi.ac.uk/efo/EFO_0009636 GCST90078830 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nasal polyps (Gene-based burden) 2,016 European ancestry cases, 329,738 European ancestry controls NA Illumina [184201] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90081824 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Underweight 2,095 European ancestry cases, 140,458 European ancestry controls NA Affymetrix, Illumina [244810] 0 underweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005936 GCST90081529 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33: nasal polyps (Gene-based burden) 1,790 European ancestry cases, 327,262 European ancestry controls NA Illumina [184145] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90081825 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Folic acid or Folate Vit B9 (UKB data field 6155) 10,077 European ancestry cases, 132,748 European ancestry controls NA Affymetrix, Illumina [244703] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90079470 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nasal sinus disorder (Gene-based burden) 1,740 European ancestry cases, 330,014 European ancestry controls NA Illumina [184201] 0 paranasal sinus disease http://www.ebi.ac.uk/efo/EFO_0009481 GCST90081818 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Multivitamins minerals (UKB data field 6155) 97,313 European ancestry cases, 45,512 European ancestry controls NA Affymetrix, Illumina [244703] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90079471 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34: nasal sinus disorder (Gene-based burden) 1,548 European ancestry cases, 327,504 European ancestry controls NA Illumina [184145] 0 paranasal sinus disease http://www.ebi.ac.uk/efo/EFO_0009481 GCST90081819 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin A (UKB data field 6155) 8,781 European ancestry cases, 134,044 European ancestry controls NA Affymetrix, Illumina [244703] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90079465 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nervous breakdown (Gene-based burden) 669 European ancestry cases, 331,085 European ancestry controls NA Illumina [184201] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90081751 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin B (UKB data field 6155) 19,958 European ancestry cases, 122,867 European ancestry controls NA Affymetrix, Illumina [244703] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90079466 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F430: nervous breakdown (Gene-based burden) 637 European ancestry cases, 328,415 European ancestry controls NA Illumina [184145] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90081752 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin C (UKB data field 6155) 39,394 European ancestry cases, 103,431 European ancestry controls NA Affymetrix, Illumina [244703] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90079467 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oesophagitis barretts oesophagus (Gene-based burden) 1,490 European ancestry cases, 330,264 European ancestry controls NA Illumina [184201] 0 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90081680 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin D (UKB data field 6155) 22,734 European ancestry cases, 120,091 European ancestry controls NA Affymetrix, Illumina [244703] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90079468 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K20: oesophagitis barretts oesophagus (Gene-based burden) 1,386 European ancestry cases, 327,666 European ancestry controls NA Illumina [184145] 0 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90081681 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin E (UKB data field 6155) 13,167 European ancestry cases, 129,658 European ancestry controls NA Affymetrix, Illumina [244703] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90079469 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81: menieres disease (Gene-based burden) 1,091 European ancestry cases, 327,961 European ancestry controls NA Illumina [184145] 0 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90081827 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 1 (UKB data field 21041) 25,550 European ancestry cases, 128,890 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078776 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Meningitis (Gene-based burden) 1,865 European ancestry cases, 329,889 European ancestry controls NA Illumina [184201] 0 infectious meningitis http://www.ebi.ac.uk/efo/EFO_0000584 GCST90081720 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 2 (UKB data field 21041) 14,163 European ancestry cases, 140,277 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078777 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G03: meningitis (Gene-based burden) 1,689 European ancestry cases, 327,363 European ancestry controls NA Illumina [184145] 0 infectious meningitis http://www.ebi.ac.uk/efo/EFO_0000584 GCST90081721 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 3 (UKB data field 21041) 8,434 European ancestry cases, 146,006 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078778 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Menorrhagia unknown cause (Gene-based burden) 1,559 European ancestry cases, 330,195 European ancestry controls NA Illumina [184201] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90081919 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 4 (UKB data field 21041) 4,573 European ancestry cases, 149,867 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078779 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92: menorrhagia unknown cause (Gene-based burden) 1,349 European ancestry cases, 176,545 European ancestry controls NA Illumina [177166] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90081920 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 5 (UKB data field 21041) 9,405 European ancestry cases, 145,035 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078780 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Migraine (Gene-based burden) 14,131 European ancestry cases, 317,623 European ancestry controls NA Illumina [184201] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90081731 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 6 (UKB data field 21041) 5,517 European ancestry cases, 148,923 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078781 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G43: Migraine (Gene-based burden) 11,475 European ancestry cases, 317,577 European ancestry controls NA Illumina [184145] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90081732 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 7 (UKB data field 21041) 5,316 European ancestry cases, 149,124 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078782 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Miscarriage (Gene-based burden) 1,373 European ancestry cases, 330,381 European ancestry controls NA Illumina [184201] 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90081921 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 8 (UKB data field 21041) 3,520 European ancestry cases, 150,920 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078783 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O04: miscarriage (Gene-based burden) 1,240 European ancestry cases, 176,654 European ancestry controls NA Illumina [177166] 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90081922 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 9 (UKB data field 21041) 1,521 European ancestry cases, 152,919 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078784 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple sclerosis (Gene-based burden) 1,596 European ancestry cases, 330,158 European ancestry controls NA Illumina [184201] 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90081725 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 10 - Completely (UKB data field 21041) 1,399 European ancestry cases, 153,041 European ancestry controls NA Affymetrix, Illumina [261672] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078775 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G35: Multiple sclerosis (Gene-based burden) 1,463 European ancestry cases, 327,589 European ancestry controls NA Illumina [184145] 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90081726 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coeliac disease or gluten sensitivity (UKB data field 21068) 2,911 European ancestry cases, 151,167 European ancestry controls NA Affymetrix, Illumina [261237] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90078832 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mumps epidemic parotitis (Gene-based burden) 3,743 European ancestry cases, 328,011 European ancestry controls NA Illumina [184201] 0 Mumps virus infectious disease http://www.ebi.ac.uk/efo/EFO_0007383 GCST90081929 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N40: benign prostatic hypertrophy 968 European ancestry cases, 150,190 European ancestry controls NA Affymetrix, Illumina [256146] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90077917 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B26: mumps epidemic parotitis (Gene-based burden) 3,260 European ancestry cases, 325,792 European ancestry controls NA Illumina [184145] 0 Mumps virus infectious disease http://www.ebi.ac.uk/efo/EFO_0007383 GCST90081930 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G20: parkinsons disease 772 European ancestry cases, 328,280 European ancestry controls NA Affymetrix, Illumina [456275] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90077742 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W10: Fall on and from stairs and steps (Gene-based burden) 3,736 European ancestry cases, 383,879 European ancestry controls NA Illumina [185342] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085094 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73: peripheral vascular disease 701 European ancestry cases, 328,351 European ancestry controls NA Affymetrix, Illumina [456275] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90077650 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W10.0: Fall on/from escalator (Gene-based burden) 2,038 European ancestry cases, 385,891 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085092 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K65: Peritonitis 1,370 European ancestry cases, 327,682 European ancestry controls NA Affymetrix, Illumina [456275] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90077709 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W10.9: Fall on/from unspecified stairs and steps (Gene-based burden) 1,246 European ancestry cases, 386,345 European ancestry controls NA Illumina [185342] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085093 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D51: pernicious anaemia 1,182 European ancestry cases, 327,870 European ancestry controls NA Affymetrix, Illumina [456275] 0 pernicious anemia http://www.ebi.ac.uk/efo/EFO_0005576 GCST90077790 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W11: Fall on/from ladder (Gene-based burden) 1,585 European ancestry cases, 386,260 European ancestry controls NA Illumina [185343] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085097 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R091: pleurisy 1,542 European ancestry cases, 327,510 European ancestry controls NA Affymetrix, Illumina [456275] 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90077684 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W11.0: Fall on/from ladder - Home (Gene-based burden) 728 European ancestry cases, 387,202 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085095 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18: pneumonia 6,178 European ancestry cases, 322,874 European ancestry controls NA Affymetrix, Illumina [456275] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90077820 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W11.9: Fall on/from ladder - Unspecified place (Gene-based burden) 745 European ancestry cases, 387,185 European ancestry controls NA Illumina [185342] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085096 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35: polymyalgia rheumatica 908 European ancestry cases, 328,144 European ancestry controls NA Affymetrix, Illumina [456275] 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90077809 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W17: Other fall from one level to another (Gene-based burden) 757 European ancestry cases, 387,116 European ancestry controls NA Illumina [185343] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085098 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51: Prolapsed disc or slipped disc 6,808 European ancestry cases, 322,244 European ancestry controls NA Affymetrix, Illumina [456275] 0 vertebral joint disease http://www.ebi.ac.uk/efo/EFO_0009477 GCST90077784 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W18: Other slipping, tripping and stumbling and falls (Gene-based burden) 2,627 European ancestry cases, 385,170 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085101 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40: Psoriasis 4,381 European ancestry cases, 324,671 European ancestry controls 4,001 European ancestry cases, 118,929 European ancestry controls Affymetrix, Illumina [456275] 1 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90077856 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W18.0: Fall due to bumping against object (Gene-based burden) 1,046 European ancestry cases, 386,883 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085099 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40: psoriatic arthropathy 762 European ancestry cases, 328,290 European ancestry controls NA Affymetrix, Illumina [456275] 0 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90077890 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W18.9: Unspecified place (Gene-based burden) 638 European ancestry cases, 387,292 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085100 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I26: Pulmonary embolism 3,235 European ancestry cases, 325,817 European ancestry controls NA Affymetrix, Illumina [456275] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90077668 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19: Unspecified fall (Gene-based burden) 8,510 European ancestry cases, 372,626 European ancestry controls NA Illumina [185212] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085106 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 0 - Very happy (UKB data field 21040) 29,522 European ancestry cases, 124,901 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078764 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Menieres disease (Gene-based burden) 1,297 European ancestry cases, 330,457 European ancestry controls NA Illumina [184201] 0 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90081826 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 10 - Very unhappy (UKB data field 21040) 4,995 European ancestry cases, 149,428 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078765 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.49: Family history of ischemic heart disease and other diseases of the circulatory system (Gene-based burden) 29,712 European ancestry cases, 309,459 European ancestry controls NA Illumina [184464] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085322 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salmeterol 1,161 European ancestry cases, 319,597 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078012 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.5: Family history of asthma and other chronic lower respiratory diseases (Gene-based burden) 2,054 European ancestry cases, 377,121 European ancestry controls NA Illumina [185188] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085324 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salmeterol fluticasone propionate 814 European ancestry cases, 319,944 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078192 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83: Family history of other specific disorders (Gene-based burden) 4,125 European ancestry cases, 372,628 European ancestry controls NA Illumina [185180] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085329 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - selenium ace tablet 581 European ancestry cases, 320,177 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078144 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83.3: Family history of diabetes mellitus (Gene-based burden) 873 European ancestry cases, 382,547 European ancestry controls NA Illumina [185282] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085326 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - selenium product 1,390 European ancestry cases, 319,368 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078112 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83.5: Family history of eye and ear disorders (Gene-based burden) 1,666 European ancestry cases, 383,607 European ancestry controls NA Illumina [185309] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085327 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - senna 874 European ancestry cases, 319,884 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078033 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83.7: Family history of diseases of the digestive system (Gene-based burden) 947 European ancestry cases, 386,486 European ancestry controls NA Illumina [185339] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085328 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - seretide 50 evohaler 5,267 European ancestry cases, 315,491 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078209 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z84: Family history of other conditions (Gene-based burden) 1,226 European ancestry cases, 379,055 European ancestry controls NA Illumina [185221] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085332 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - serevent inhaler 1,172 European ancestry cases, 319,586 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078013 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z84.8: Family history of other specified conditions (Gene-based burden) 1,025 European ancestry cases, 380,498 European ancestry controls NA Illumina [185239] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085331 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sertraline 2,205 European ancestry cases, 318,553 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078041 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z84.89: Family history of other specified conditions (Gene-based burden) 920 European ancestry cases, 380,626 European ancestry controls NA Illumina [185239] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90085330 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - simvador 595 European ancestry cases, 320,163 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078222 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85: Personal history of malignant neoplasm (Gene-based burden) 30,873 European ancestry cases, 356,515 European ancestry controls NA Illumina [185338] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90085340 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - simvastatin 51,781 European ancestry cases, 268,977 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078009 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.0: Personal history of malignant neoplasm of digestive organs (Gene-based burden) 6,500 European ancestry cases, 381,416 European ancestry controls NA Illumina [185344] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90085333 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - solifenacin 833 European ancestry cases, 319,925 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078232 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.1: Personal history of malignant neoplasm of trachea, bronchus and lung (Gene-based burden) 884 European ancestry cases, 387,044 European ancestry controls NA Illumina [185344] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90085334 Exome-wide sequencing 2021-05-19 33074286 Kunkle BW 2020-10-19 JAMA Neurol www.ncbi.nlm.nih.gov/pubmed/33074286 Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis. Alzheimer's disease 2,784 African American cases, 5,222 African American controls NA Illumina [29610185] (imputed) 15 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST011696 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sotalol 675 European ancestry cases, 320,083 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078099 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.3: Personal history of malignant neoplasm of breast (Gene-based burden) 8,566 European ancestry cases, 379,356 European ancestry controls NA Illumina [185344] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90085335 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - more than 100 times (UKB data field 20453) 3,721 European ancestry cases, 135,790 European ancestry controls NA Affymetrix, Illumina [241053] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90078475 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peritonitis (Gene-based burden) 1,501 European ancestry cases, 330,253 European ancestry controls NA Illumina [184201] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90081694 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - 1 to 2 times (UKB data field 20453) 13,223 European ancestry cases, 126,288 European ancestry controls NA Affymetrix, Illumina [241053] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90078472 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K65: Peritonitis (Gene-based burden) 1,370 European ancestry cases, 327,682 European ancestry controls NA Illumina [184145] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90081695 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - 3 to 10 times (UKB data field 20453) 7,724 European ancestry cases, 131,787 European ancestry controls NA Affymetrix, Illumina [241053] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90078473 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pernicious anaemia (Gene-based burden) 1,382 European ancestry cases, 330,372 European ancestry controls NA Illumina [184201] 0 pernicious anemia http://www.ebi.ac.uk/efo/EFO_0005576 GCST90081775 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - A little bit (UKB data field 20498) 39,340 European ancestry cases, 100,162 European ancestry controls NA Affymetrix, Illumina [241049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078550 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D51: pernicious anaemia (Gene-based burden) 1,182 European ancestry cases, 327,870 European ancestry controls NA Illumina [184145] 0 pernicious anemia http://www.ebi.ac.uk/efo/EFO_0005576 GCST90081776 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - Extremely (UKB data field 20498) 1,284 European ancestry cases, 138,218 European ancestry controls NA Affymetrix, Illumina [241049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078553 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pleurisy (Gene-based burden) 1,711 European ancestry cases, 330,043 European ancestry controls NA Illumina [184201] 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90081669 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - Moderately (UKB data field 20498) 7,409 European ancestry cases, 132,093 European ancestry controls NA Affymetrix, Illumina [241049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078551 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R091: pleurisy (Gene-based burden) 1,542 European ancestry cases, 327,510 European ancestry controls NA Illumina [184145] 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90081670 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - Quite a bit (UKB data field 20498) 4,459 European ancestry cases, 135,043 European ancestry controls NA Affymetrix, Illumina [241049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078552 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pneumonia (Gene-based burden) 6,965 European ancestry cases, 324,789 European ancestry controls NA Illumina [184201] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90081805 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - Monthly or less (UKB data field 20414) 17,982 European ancestry cases, 121,560 European ancestry controls NA Affymetrix, Illumina [241043] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078427 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18: pneumonia (Gene-based burden) 6,178 European ancestry cases, 322,874 European ancestry controls NA Illumina [184145] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90081806 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - Never (UKB data field 20414) 11,380 European ancestry cases, 128,162 European ancestry controls NA Affymetrix, Illumina [241043] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078426 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Polycystic ovaries polycystic ovarian syndrome (Gene-based burden) 573 European ancestry cases, 331,181 European ancestry controls NA Illumina [184108] 0 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST90081781 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Polymyalgia rheumatica (Gene-based burden) 1,059 European ancestry cases, 330,695 European ancestry controls NA Illumina [184201] 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90081794 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.0: Personal history of diseases of the respiratory system (Gene-based burden) 4,223 European ancestry cases, 376,238 European ancestry controls NA Illumina [185228] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90085353 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tolterodine left tartrate 902 European ancestry cases, 319,856 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078190 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.09: Personal history of other diseases of the respiratory system (Gene-based burden) 2,125 European ancestry cases, 378,842 European ancestry controls NA Illumina [185234] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90085352 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tramadol 4,956 European ancestry cases, 315,802 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078026 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.1: Personal history of diseases of the digestive system (Gene-based burden) 20,497 European ancestry cases, 366,069 European ancestry controls NA Illumina [185322] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90085354 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - trazodone 633 European ancestry cases, 320,125 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078090 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other renal or kidney problem (Gene-based burden) 1,957 European ancestry cases, 329,797 European ancestry controls NA Illumina [184201] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90081810 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been injured or injured someone else through drinking alcohol during the last year (UKB data field 20411) 644 European ancestry cases, 138,996 European ancestry controls NA Affymetrix, Illumina [241221] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90078420 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28: Other renal or kidney problem (Gene-based burden) 1,807 European ancestry cases, 327,245 European ancestry controls NA Illumina [184145] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90081811 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - A little bit (UKB data field 20497) 28,097 European ancestry cases, 111,415 European ancestry controls NA Affymetrix, Illumina [241066] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90078546 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other respiratory problems (Gene-based burden) 759 European ancestry cases, 330,995 European ancestry controls NA Illumina [184201] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90081665 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - Extremely (UKB data field 20497) 914 European ancestry cases, 138,598 European ancestry controls NA Affymetrix, Illumina [241066] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90078549 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98: other respiratory problems (Gene-based burden) 685 European ancestry cases, 328,367 European ancestry controls NA Illumina [184145] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90081666 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - Moderately (UKB data field 20497) 5,330 European ancestry cases, 134,182 European ancestry controls NA Affymetrix, Illumina [241066] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90078547 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ovarian cyst or cysts (Gene-based burden) 3,831 European ancestry cases, 327,923 European ancestry controls NA Illumina [184201] 0 Ovarian cyst http://purl.obolibrary.org/obo/HP_0000138 GCST90081779 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - Quite a bit (UKB data field 20497) 3,952 European ancestry cases, 135,560 European ancestry controls NA Affymetrix, Illumina [241066] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90078548 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83: ovarian cyst or cysts (Gene-based burden) 3,353 European ancestry cases, 174,541 European ancestry controls NA Illumina [177166] 0 Tarlov Cysts http://www.ebi.ac.uk/efo/EFO_1001858 GCST90081780 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble concentrating on things - More than half the days (UKB data field 20508) 2,878 European ancestry cases, 136,635 European ancestry controls NA Affymetrix, Illumina [241064] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078569 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pancreatitis (Gene-based burden) 980 European ancestry cases, 330,774 European ancestry controls NA Illumina [184201] 0 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90081692 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble concentrating on things - Nearly every day (UKB data field 20508) 2,356 European ancestry cases, 137,157 European ancestry controls NA Affymetrix, Illumina [241064] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078570 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K85: pancreatitis (Gene-based burden) 868 European ancestry cases, 328,184 European ancestry controls NA Illumina [184145] 0 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90081693 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble concentrating on things - Several days (UKB data field 20508) 20,324 European ancestry cases, 119,189 European ancestry controls NA Affymetrix, Illumina [241064] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078568 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Parkinsons disease (Gene-based burden) 828 European ancestry cases, 330,926 European ancestry controls NA Illumina [184201] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90081727 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent poor appetite or overeating - More than half the days (UKB data field 20511) 3,964 European ancestry cases, 135,560 European ancestry controls NA Affymetrix, Illumina [241055] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078581 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G20: parkinsons disease (Gene-based burden) 772 European ancestry cases, 328,280 European ancestry controls NA Illumina [184145] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90081728 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent poor appetite or overeating - Nearly every day (UKB data field 20511) 3,494 European ancestry cases, 136,030 European ancestry controls NA Affymetrix, Illumina [241055] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078582 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peripheral neuropathy (Gene-based burden) 691 European ancestry cases, 331,063 European ancestry controls NA Illumina [184201] 0 peripheral neuropathy http://www.ebi.ac.uk/efo/EFO_0003100 GCST90081722 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent poor appetite or overeating - Several days (UKB data field 20511) 18,394 European ancestry cases, 121,130 European ancestry controls NA Affymetrix, Illumina [241055] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078580 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peripheral vascular disease (Gene-based burden) 813 European ancestry cases, 330,941 European ancestry controls NA Illumina [184201] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90081635 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - 11 to 100 times (UKB data field 20453) 6,210 European ancestry cases, 133,301 European ancestry controls NA Affymetrix, Illumina [241053] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90078474 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73: peripheral vascular disease (Gene-based burden) 701 European ancestry cases, 328,351 European ancestry controls NA Illumina [184145] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90081636 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.69: Personal history of other diseases of the nervous system and sense organs (Gene-based burden) 1,115 European ancestry cases, 385,013 European ancestry controls NA Illumina [185329] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085347 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - thyroxine product 5,384 European ancestry cases, 315,374 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078118 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.7: Personal history of diseases of the circulatory system (Gene-based burden) 22,886 European ancestry cases, 360,766 European ancestry controls NA Illumina [185283] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90085350 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - thyroxine sodium 1,240 European ancestry cases, 319,518 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078074 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.79: Personal history of other diseases of the circulatory system (Gene-based burden) 1,822 European ancestry cases, 382,036 European ancestry controls NA Illumina [185283] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90085349 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tildiem m/right tablet 866 European ancestry cases, 319,892 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078004 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87: Personal history of other diseases and conditions (Gene-based burden) 81,773 European ancestry cases, 279,736 European ancestry controls NA Illumina [184884] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085366 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tiotropium 1,157 European ancestry cases, 319,601 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078218 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - 2 to 4 times a month (UKB data field 20414) 25,530 European ancestry cases, 114,012 European ancestry controls NA Affymetrix, Illumina [241043] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078428 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M89: osteopenia (Gene-based burden) 1,458 European ancestry cases, 327,593 European ancestry controls NA Illumina [184145] 0 Osteopenia http://purl.obolibrary.org/obo/HP_0000938 GCST90081948 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg deep vein thrombosis (UKB data field 6152) 9,223 European ancestry cases, 131,738 European ancestry controls NA Affymetrix, Illumina [243196] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90079453 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Long term recurrent antibiotics as child or teenager (UKB data field 21067) 20,435 European ancestry cases, 120,320 European ancestry controls NA Affymetrix, Illumina [242819] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078831 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - spiriva 672 European ancestry cases, 320,086 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078219 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.4: Personal history of malignant neoplasm of genital organs (Gene-based burden) 5,672 European ancestry cases, 382,236 European ancestry controls NA Illumina [185344] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90085336 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - spironolactone 859 European ancestry cases, 319,899 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078038 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.5: Personal history of malignant neoplasm of urinary tract (Gene-based burden) 3,617 European ancestry cases, 384,280 European ancestry controls NA Illumina [185344] 0 Malignant Urinary System Neoplasm http://www.ebi.ac.uk/efo/EFO_1000363 GCST90085337 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - st johns wort/hypericum 773 European ancestry cases, 319,985 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078239 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.7: Personal history of other malignant neoplasms of lymphoid, hematopoietic and related tissues (Gene-based burden) 1,462 European ancestry cases, 386,468 European ancestry controls NA Illumina [185344] 0 GCST90085338 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - starflower oil 668 European ancestry cases, 320,090 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078143 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.8: Personal history of malignant neoplasms of other organs and systems (Gene-based burden) 7,665 European ancestry cases, 380,238 European ancestry controls NA Illumina [185344] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90085339 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sulfasalazine 862 European ancestry cases, 319,896 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078135 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86: Personal history of certain other diseases (Gene-based burden) 68,491 European ancestry cases, 310,419 European ancestry controls NA Illumina [185205] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085351 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sumatriptan 1,299 European ancestry cases, 319,459 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078114 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.0: Personal history of in-situ and benign neoplasms and neoplasms of uncertain behavior (Gene-based burden) 6,926 European ancestry cases, 381,003 European ancestry controls NA Illumina [185344] 0 GCST90085341 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - symbicort turbohaler 2,812 European ancestry cases, 317,946 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078206 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.1: Personal history of infectious and parasitic diseases (Gene-based burden) 2,974 European ancestry cases, 382,859 European ancestry controls NA Illumina [185295] 0 parasitic infection http://www.ebi.ac.uk/efo/EFO_0001067 GCST90085342 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tamoxifen 1,471 European ancestry cases, 319,287 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078053 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.2: Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (Gene-based burden) 866 European ancestry cases, 384,120 European ancestry controls NA Illumina [185302] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085343 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tegretol 952 European ancestry cases, 319,806 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078066 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.3: Personal history of endocrine, nutritional and metabolic diseases (Gene-based burden) 576 European ancestry cases, 386,857 European ancestry controls NA Illumina [185328] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085344 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - telmisartan 698 European ancestry cases, 320,060 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078194 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.4: Personal history of psychoactive substance abuse (Gene-based burden) 39,220 European ancestry cases, 348,710 European ancestry controls NA Illumina [185344] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085345 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - temazepam 901 European ancestry cases, 319,857 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078023 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.5: Personal history of mental and behavioral disorders (Gene-based burden) 1,209 European ancestry cases, 386,498 European ancestry controls NA Illumina [185343] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90085346 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - terbinafine 923 European ancestry cases, 319,835 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078170 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.6: Personal history of diseases of the nervous system and sense organs (Gene-based burden) 10,198 European ancestry cases, 376,004 European ancestry controls NA Illumina [185330] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085348 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - terbutaline 664 European ancestry cases, 320,094 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078094 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.2: Personal history of diseases of the skin and subcutaneous tissue (Gene-based burden) 1,460 European ancestry cases, 383,809 European ancestry controls NA Illumina [185285] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90085355 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - valsartan 2,102 European ancestry cases, 318,656 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078173 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.3: Personal history of diseases of the musculoskeletal system and connective tissue (Gene-based burden) 3,459 European ancestry cases, 379,603 European ancestry controls NA Illumina [185283] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085357 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - venlafaxine 1,845 European ancestry cases, 318,913 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078149 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.39: Personal history of other diseases of the musculoskeletal system and connective tissue (Gene-based burden) 896 European ancestry cases, 382,287 European ancestry controls NA Illumina [185284] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085356 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ventolin inhaler 13,099 European ancestry cases, 307,659 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078010 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.4: Personal history of diseases of genitourinary system (Gene-based burden) 9,978 European ancestry cases, 373,090 European ancestry controls NA Illumina [185252] 0 disease of genitourinary system http://www.ebi.ac.uk/efo/EFO_0009663 GCST90085359 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - verapamil 764 European ancestry cases, 319,994 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078126 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.42: Personal history of other diseases of the female genital tract (Gene-based burden) 837 European ancestry cases, 383,615 European ancestry controls NA Illumina [185263] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90085358 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - viscotears liquid eye gel 1,058 European ancestry cases, 319,700 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078027 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.7: Personal history of (corrected) congenital malformations (Gene-based burden) 524 European ancestry cases, 387,359 European ancestry controls NA Illumina [75235] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085360 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin b compound 3,325 European ancestry cases, 317,433 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078060 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.8: Personal history of other specified conditions (Gene-based burden) 50,319 European ancestry cases, 321,392 European ancestry controls NA Illumina [185083] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085365 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin b12 preparation 1,484 European ancestry cases, 319,274 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078056 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.82: Personal history of other (healed) physical injury and trauma (Gene-based burden) 1,098 European ancestry cases, 381,734 European ancestry controls NA Illumina [185279] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085362 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin c product 5,639 European ancestry cases, 315,119 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078137 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.828.: Personal history of other (healed) physical injury and trauma (Gene-based burden) 1,098 European ancestry cases, 381,734 European ancestry controls NA Illumina [185279] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085361 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin c product 1,280 European ancestry cases, 319,478 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078236 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.89: Personal history of other specified conditions (Gene-based burden) 48,740 European ancestry cases, 326,162 European ancestry controls NA Illumina [185135] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90085364 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin d product 2,010 European ancestry cases, 318,748 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078059 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.891.: Personal history of nicotine dependence (Gene-based burden) 48,661 European ancestry cases, 326,806 European ancestry controls NA Illumina [185145] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90085363 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin e product 1,685 European ancestry cases, 319,073 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078062 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88: Allergy status to drugs, medicaments and biological substances (Gene-based burden) 36,339 European ancestry cases, 339,428 European ancestry controls NA Illumina [185143] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085374 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - warfarin 4,740 European ancestry cases, 316,018 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078123 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.0: Allergy status to penicillin (Gene-based burden) 20,233 European ancestry cases, 365,807 European ancestry controls NA Illumina [185327] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085367 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteoporosis (Gene-based burden) 7,730 European ancestry cases, 324,024 European ancestry controls NA Illumina [184201] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90081765 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81: osteoporosis (Gene-based burden) 6,633 European ancestry cases, 322,419 European ancestry controls NA Illumina [184145] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90081766 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - aunt (UKB data field 4979) 17,526 European ancestry cases, 121,844 European ancestry controls NA Affymetrix, Illumina [241686] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079243 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other abdominal problem (Gene-based burden) 528 European ancestry cases, 331,226 European ancestry controls NA Illumina [184201] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90081677 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - cousin (UKB data field 4979) 86,002 European ancestry cases, 53,368 European ancestry controls NA Affymetrix, Illumina [241686] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079246 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other joint disorder (Gene-based burden) 2,706 European ancestry cases, 329,048 European ancestry controls NA Illumina [184201] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90081865 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - niece (UKB data field 4979) 21,550 European ancestry cases, 117,820 European ancestry controls NA Affymetrix, Illumina [241686] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079245 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: other joint disorder (Gene-based burden) 2,283 European ancestry cases, 326,769 European ancestry controls NA Illumina [184145] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90081866 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - no relation (UKB data field 4979) 8,036 European ancestry cases, 131,334 European ancestry controls NA Affymetrix, Illumina [241686] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079247 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other neurological problem (Gene-based burden) 1,794 European ancestry cases, 329,960 European ancestry controls NA Illumina [184201] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90081828 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - sister (UKB data field 4979) 13,858 European ancestry cases, 125,512 European ancestry controls NA Affymetrix, Illumina [241686] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079244 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G98: other neurological problem (Gene-based burden) 1,701 European ancestry cases, 327,351 European ancestry controls NA Illumina [184145] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90081829 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been injured or injured someone else through drinking alcohol but not in the last year (UKB data field 20411) 5,296 European ancestry cases, 134,344 European ancestry controls NA Affymetrix, Illumina [241221] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90078419 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-07-05 33239738 Didriksen M 2020-11-25 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33239738 Large genome-wide association study identifies three novel risk variants for restless legs syndrome. Restless legs syndrome 10,257 European ancestry cases, 470,725 European ancestry controls up to 15,126 European ancestry cases, up to 95,725 European ancestry controls Affymetrix, Illumina [15838848] (imputed) 25 restless legs syndrome http://www.ebi.ac.uk/efo/EFO_0004270 GCST011995 Genome-wide genotyping array 2021-06-23 33290381 Li W 2020-12-07 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/33290381 The influence of regression models on genome-wide association studies of alcohol dependence: a comparison of binary and quantitative analyses. Alcohol dependence 739 European ancestry cases, 1,251 European ancestry controls NA Illumina [2100000] (imputed) 7 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST011955 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Cardio-cerebrovascular disease in hypertension 1,185 Korean ancestry cases, 15,117 Korean ancestry controls NA Affymetrix [7975321] (imputed) 11 Ischemic stroke, coronary artery disease http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90014124 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Coronary artery disease in hypertension 816 Korean ancestry cases, 15,488 Korean ancestry controls NA Affymetrix [7975321] (imputed) 22 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90014125 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Ischemic stroke in hypertension 398 Korean ancestry cases, 15,909 Korean ancestry controls NA Affymetrix [7975321] (imputed) 26 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90014126 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Cardio-cerebrovascular disease in diabetes mellitus 497 Korean ancestry cases, 4,815 Korean ancestry controls NA Affymetrix [7975321] (imputed) 28 Ischemic stroke, coronary artery disease http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90014127 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Coronary artery disease in diabetes 361 Korean ancestry cases, 4,951 Korean ancestry controls NA Affymetrix [7975321] (imputed) 24 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90014128 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Ischemic stroke in diabetes mellitus 153 Korean ancestry cases, 5,161 Korean ancestry controls NA Affymetrix [7975321] (imputed) 51 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90014129 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Cardio-cerebrovascular disease in dyslipidemia 1,039 Korean ancestry cases, 19,727 Korean ancestry controls NA Affymetrix [7975321] (imputed) 22 Ischemic stroke, coronary artery disease http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90014130 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Coronary artery disease in dyslipidemia 768 Korean ancestry cases, 19,999 Korean ancestry controls NA Affymetrix [7975321] (imputed) 29 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90014131 Genome-wide genotyping array 2021-03-22 33632238 Song Y 2021-02-25 J Transl Med www.ncbi.nlm.nih.gov/pubmed/33632238 Identification of susceptibility loci for cardiovascular disease in adults with hypertension, diabetes, and dyslipidemia. Ischemic stroke in dyslipidemia 295 Korean ancestry cases, 20,474 Korean ancestry controls NA Affymetrix [7975321] (imputed) 45 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90014132 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coronary artery disease 28,605 European ancestry cases, 254,598 European ancestry controls 19,813 European ancestry cases, 98,285 European ancestry controls Affymetrix, Illumina [410331] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90081466 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.890.: Other specified postprocedural states (Gene-based burden) 10,483 European ancestry cases, 355,405 European ancestry controls NA Illumina [184959] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085423 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Foot measured for bone density - left (UKB data field 3081) 280,489 European ancestry cases, 3,638 European ancestry controls NA Affymetrix, Illumina [408253] 0 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90079038 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99: Dependence on enabling machines and devices, not elsewhere classified (Gene-based burden) 3,699 European ancestry cases, 381,774 European ancestry controls NA Illumina [185292] 0 dependence on enabling machines and devices http://www.ebi.ac.uk/efo/EFO_0020981 GCST90085431 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Foot measured for bone density - right (UKB data field 3081) 3,638 European ancestry cases, 280,489 European ancestry controls NA Affymetrix, Illumina [408253] 0 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90079039 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.1: Dependence on respirator (Gene-based burden) 567 European ancestry cases, 387,362 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085427 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ischemic stroke 6,260 European ancestry cases, 270,409 European ancestry controls NA Affymetrix, Illumina [403974] 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90081456 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.2: Dependence on renal dialysis (Gene-based burden) 1,868 European ancestry cases, 383,685 European ancestry controls NA Illumina [185292] 0 renal dialysis http://www.ebi.ac.uk/efo/EFO_0010690 GCST90085428 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Atopic dermatitis 15,131 European ancestry cases, 261,539 European ancestry controls 1,810 European ancestry cases, 108,305 European ancestry controls Affymetrix, Illumina [403215] 0 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90081462 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.3: Dependence on wheelchair (Gene-based burden) 762 European ancestry cases, 387,143 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085429 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Back pain (UKB data field 6159) 116,024 European ancestry cases, 149,919 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079481 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.8: Dependence on other enabling machines and devices (Gene-based burden) 635 European ancestry cases, 387,219 European ancestry controls NA Illumina [185344] 0 dependence on enabling machines and devices http://www.ebi.ac.uk/efo/EFO_0020981 GCST90085430 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Facial pain (UKB data field 6159) 8,530 European ancestry cases, 257,413 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079479 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. IGF 1 (UKB data field 30770) (Gene-based burden) 409,926 European ancestry individuals NA Illumina [185626] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90083018 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Headache (UKB data field 6159) 89,640 European ancestry cases, 176,303 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079478 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Bowel cancer (UKB data field 20107) (Gene-based burden) 22,536 European ancestry cases, 397,061 European ancestry controls NA Illumina [185792] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082246 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Hip pain (UKB data field 6159) 52,712 European ancestry cases, 213,231 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079483 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Chronic bronchitis emphysema (UKB data field 20107) (Gene-based burden) 44,472 European ancestry cases, 375,126 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082247 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Knee pain (UKB data field 6159) 98,206 European ancestry cases, 167,737 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079484 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Diabetes (UKB data field 20107) (Gene-based burden) 36,789 European ancestry cases, 382,809 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082249 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Neck or shoulder pain (UKB data field 6159) 104,510 European ancestry cases, 161,433 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079480 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Heart disease (UKB data field 20107) (Gene-based burden) 127,319 European ancestry cases, 292,279 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082243 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Pain all over the body (UKB data field 6159) 7,206 European ancestry cases, 258,737 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079485 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - High blood pressure (UKB data field 20107) (Gene-based burden) 87,674 European ancestry cases, 331,924 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082248 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Stomach or abdominal pain (UKB data field 6159) 38,802 European ancestry cases, 227,141 European ancestry controls NA Affymetrix, Illumina [393430] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079482 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.0: Presence of urogenital implants (Gene-based burden) 2,038 European ancestry cases, 385,858 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085412 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 2 and 3 hours (UKB data field 981) 23,530 European ancestry cases, 289,247 European ancestry controls NA Affymetrix, Illumina [440320] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079530 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.1: Presence of intraocular lens (Gene-based burden) 8,165 European ancestry cases, 379,112 European ancestry controls NA Illumina [185331] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085413 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Over 3 hours (UKB data field 981) 23,324 European ancestry cases, 289,453 European ancestry controls NA Affymetrix, Illumina [440320] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079531 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.6: Presence of orthopedic joint implants (Gene-based burden) 14,119 European ancestry cases, 373,799 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085414 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adult asthma vs allergic disease 26,201 European ancestry cases, 280,679 European ancestry controls NA Affymetrix, Illumina [435128] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081449 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.8: Presence of other specified functional implants (Gene-based burden) 1,112 European ancestry cases, 386,818 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085415 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inflammatory bowel disease 5,650 European ancestry cases, 298,738 European ancestry controls NA Affymetrix, Illumina [431605] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90081491 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97: Presence of other devices (Gene-based burden) 3,870 European ancestry cases, 380,268 European ancestry controls NA Illumina [185271] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085420 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Aortic stenosis 3,900 European ancestry cases, 300,255 European ancestry controls NA Affymetrix, Illumina [431363] 0 aortic stenosis http://www.ebi.ac.uk/efo/EFO_0000266 GCST90081458 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97.4: Presence of external hearing-aid (Gene-based burden) 533 European ancestry cases, 386,972 European ancestry controls NA Illumina [185336] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085417 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rheumatoid arthritis 8,561 European ancestry cases, 295,029 European ancestry controls NA Affymetrix, Illumina [430877] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90081504 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97.5: Presence of (intrauterine) contraceptive device (Gene-based burden) 1,276 European ancestry cases, 208,800 European ancestry controls NA Illumina [179825] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085418 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - microgynon 633 European ancestry cases, 320,125 European ancestry controls NA Affymetrix, Illumina [426659] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078049 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97.8: Presence of other specified devices (Gene-based burden) 1,814 European ancestry cases, 384,875 European ancestry controls NA Illumina [185324] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085419 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Childhood asthma vs allergic disease 16,952 European ancestry cases, 280,473 European ancestry controls NA Affymetrix, Illumina [425686] 1 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90081473 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98: Other postprocedural states (Gene-based burden) 15,101 European ancestry cases, 349,629 European ancestry controls NA Illumina [184938] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085426 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing loss 98,675 European ancestry cases, 196,355 European ancestry controls 5,362 European ancestry cases, 107,415 European ancestry controls Affymetrix, Illumina [421868] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90081539 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.0: Intestinal bypass and anastomosis status (Gene-based burden) 2,891 European ancestry cases, 385,037 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085421 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - seroxat 589 European ancestry cases, 320,169 European ancestry controls NA Affymetrix, Illumina [418636] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078102 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.1: Arthrodesis status (Gene-based burden) 786 European ancestry cases, 387,058 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085422 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stroke 18,075 European ancestry cases, 272,229 European ancestry controls NA Affymetrix, Illumina [417592] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90081457 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.8: Other specified postprocedural states (Gene-based burden) 11,319 European ancestry cases, 354,570 European ancestry controls NA Illumina [184957] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085425 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing aid user (UKB data field 3393) 15,741 European ancestry cases, 266,238 European ancestry controls NA Affymetrix, Illumina [411475] 1 able to hear with hearing aids http://www.ebi.ac.uk/efo/EFO_0009720 GCST90079053 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.89: Other specified postprocedural states (Gene-based burden) 10,483 European ancestry cases, 355,404 European ancestry controls NA Illumina [184959] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085424 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - A little bit (UKB data field 20495) 20,913 European ancestry cases, 118,564 European ancestry controls NA Affymetrix, Illumina [240999] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90078538 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prostate problem (not cancer) (Gene-based burden) 774 European ancestry cases, 330,980 European ancestry controls NA Illumina [184167] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90081704 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - Extremely (UKB data field 20495) 876 European ancestry cases, 138,601 European ancestry controls NA Affymetrix, Illumina [240999] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90078541 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N42: prostate problem (not cancer) (Gene-based burden) 730 European ancestry cases, 150,428 European ancestry controls NA Illumina [172888] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90081705 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - Moderately (UKB data field 20495) 4,057 European ancestry cases, 135,420 European ancestry controls NA Affymetrix, Illumina [240999] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90078539 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Psoriasis (Gene-based burden) 5,389 European ancestry cases, 326,365 European ancestry controls NA Illumina [184201] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90081841 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - Quite a bit (UKB data field 20495) 2,952 European ancestry cases, 136,525 European ancestry controls NA Affymetrix, Illumina [240999] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90078540 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40: Psoriasis (Gene-based burden) 4,381 European ancestry cases, 324,671 European ancestry controls NA Illumina [184145] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90081842 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - More than half the days (UKB data field 20518) 1,124 European ancestry cases, 138,348 European ancestry controls NA Affymetrix, Illumina [240994] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90078603 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Psoriatic arthropathy (Gene-based burden) 870 European ancestry cases, 330,884 European ancestry controls NA Illumina [184201] 0 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90081875 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - Nearly every day (UKB data field 20518) 857 European ancestry cases, 138,615 European ancestry controls NA Affymetrix, Illumina [240994] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90078604 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40: psoriatic arthropathy (Gene-based burden) 762 European ancestry cases, 328,290 European ancestry controls NA Illumina [184145] 0 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90081876 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - Not at all (UKB data field 20518) 131,513 European ancestry cases, 7,959 European ancestry controls NA Affymetrix, Illumina [240994] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90078601 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulmonary embolism (Gene-based burden) 3,685 European ancestry cases, 328,069 European ancestry controls NA Illumina [184201] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90081653 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - Several days (UKB data field 20518) 5,978 European ancestry cases, 133,494 European ancestry controls NA Affymetrix, Illumina [240994] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90078602 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I26: Pulmonary embolism (Gene-based burden) 3,235 European ancestry cases, 325,817 European ancestry controls NA Illumina [184145] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90081654 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling or staying asleep or sleeping too much - More than half the days (UKB data field 20517) 10,002 European ancestry cases, 129,417 European ancestry controls NA Affymetrix, Illumina [240909] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90078599 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Raynauds phenomenon disease (Gene-based burden) 628 European ancestry cases, 331,126 European ancestry controls NA Illumina [184201] 0 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90081923 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling or staying asleep or sleeping too much - Nearly every day (UKB data field 20517) 11,208 European ancestry cases, 128,211 European ancestry controls NA Affymetrix, Illumina [240909] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90078600 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73: raynauds phenomenon disease (Gene-based burden) 532 European ancestry cases, 328,520 European ancestry controls NA Illumina [184145] 0 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90081924 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling or staying asleep or sleeping too much - Several days (UKB data field 20517) 47,737 European ancestry cases, 91,682 European ancestry controls NA Affymetrix, Illumina [240909] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90078598 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rectal or colon adenoma polyps (Gene-based burden) 1,530 European ancestry cases, 330,224 European ancestry controls NA Illumina [184201] 0 adenomatous colon polyp http://www.ebi.ac.uk/efo/EFO_1000633 GCST90081853 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of tiredness or low energy - More than half the days (UKB data field 20519) 7,684 European ancestry cases, 131,738 European ancestry controls NA Affymetrix, Illumina [240891] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078606 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12: rectal or colon adenoma polyps (Gene-based burden) 1,492 European ancestry cases, 327,560 European ancestry controls NA Illumina [184145] 0 adenomatous colon polyp http://www.ebi.ac.uk/efo/EFO_1000633 GCST90081854 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of tiredness or low energy - Nearly every day (UKB data field 20519) 7,815 European ancestry cases, 131,607 European ancestry controls NA Affymetrix, Illumina [240891] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078607 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Retinal detachment (Gene-based burden) 1,666 European ancestry cases, 330,088 European ancestry controls NA Illumina [184201] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90081745 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of tiredness or low energy - Several days (UKB data field 20519) 54,906 European ancestry cases, 84,516 European ancestry controls NA Affymetrix, Illumina [240891] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078605 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33: retinal detachment (Gene-based burden) 1,460 European ancestry cases, 327,592 European ancestry controls NA Illumina [184145] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90081746 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent restlessness - More than half the days (UKB data field 20516) 1,888 European ancestry cases, 137,492 European ancestry controls NA Affymetrix, Illumina [240874] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078596 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Retinal problem (Gene-based burden) 798 European ancestry cases, 330,956 European ancestry controls NA Illumina [184201] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90081736 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent restlessness - Nearly every day (UKB data field 20516) 1,553 European ancestry cases, 137,827 European ancestry controls NA Affymetrix, Illumina [240874] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078597 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35: retinal problem (Gene-based burden) 678 European ancestry cases, 328,374 European ancestry controls NA Illumina [184145] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90081737 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent restlessness - Several days (UKB data field 20516) 13,527 European ancestry cases, 125,853 European ancestry controls NA Affymetrix, Illumina [240874] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078595 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rheumatic fever (Gene-based burden) 1,372 European ancestry cases, 330,382 European ancestry controls NA Illumina [184201] 0 rheumatic fever http://www.ebi.ac.uk/efo/EFO_1001160 GCST90081879 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Extremely happy (UKB data field 20459) 12,364 European ancestry cases, 126,997 European ancestry controls NA Affymetrix, Illumina [240838] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078486 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I00: rheumatic fever (Gene-based burden) 1,208 European ancestry cases, 327,844 European ancestry controls NA Illumina [184145] 0 rheumatic fever http://www.ebi.ac.uk/efo/EFO_1001160 GCST90081880 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Extremely unhappy (UKB data field 20459) 1,675 European ancestry cases, 137,686 European ancestry controls NA Affymetrix, Illumina [240838] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078491 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rheumatoid arthritis (Gene-based burden) 5,095 European ancestry cases, 326,659 European ancestry controls NA Illumina [184201] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90081859 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Moderately happy (UKB data field 20459) 57,988 European ancestry cases, 81,373 European ancestry controls NA Affymetrix, Illumina [240838] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078488 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06: rheumatoid arthritis (Gene-based burden) 4,752 European ancestry cases, 324,300 European ancestry controls NA Illumina [184145] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90081860 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Moderately unhappy (UKB data field 20459) 12,672 European ancestry cases, 126,689 European ancestry controls NA Affymetrix, Illumina [240838] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078489 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rosacea (Gene-based burden) 984 European ancestry cases, 330,770 European ancestry controls NA Illumina [184201] 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90081971 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Very happy (UKB data field 20459) 51,255 European ancestry cases, 88,106 European ancestry controls NA Affymetrix, Illumina [240838] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078487 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L71: Rosacea (Gene-based burden) 754 European ancestry cases, 328,298 European ancestry controls NA Illumina [184145] 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90081972 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Very unhappy (UKB data field 20459) 3,407 European ancestry cases, 135,954 European ancestry controls NA Affymetrix, Illumina [240838] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078490 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rubella german measles (Gene-based burden) 2,248 European ancestry cases, 329,506 European ancestry controls NA Illumina [184201] 0 rubella http://www.ebi.ac.uk/efo/EFO_1002026 GCST90081931 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever believed in an unreal conspiracy against self (UKB data field 20468) 1,103 European ancestry cases, 138,270 European ancestry controls NA Affymetrix, Illumina [240832] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078506 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B06: rubella german measles (Gene-based burden) 1,961 European ancestry cases, 327,091 European ancestry controls NA Illumina [184145] 0 rubella http://www.ebi.ac.uk/efo/EFO_1002026 GCST90081932 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent lack of interest or pleasure in doing things - More than half the days (UKB data field 20514) 3,128 European ancestry cases, 136,224 European ancestry controls NA Affymetrix, Illumina [240821] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078590 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sarcoidosis (Gene-based burden) 898 European ancestry cases, 330,856 European ancestry controls NA Illumina [184201] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90081790 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.7: Acquired absence of genital organ(s) (Gene-based burden) 7,830 European ancestry cases, 377,764 European ancestry controls NA Illumina [185324] 0 organ extraction http://www.ebi.ac.uk/efo/EFO_0009124 GCST90085380 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - hydrocortisone 842 European ancestry cases, 319,916 European ancestry controls NA Affymetrix, Illumina [447990] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078075 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91: Personal risk factors, not elsewhere classified (Gene-based burden) 13,623 European ancestry cases, 349,764 European ancestry controls NA Illumina [184952] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90085389 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - omacor 566 European ancestry cases, 320,192 European ancestry controls NA Affymetrix, Illumina [447990] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078217 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.0: Allergy status, other than to drugs and biological substances (Gene-based burden) 5,096 European ancestry cases, 378,727 European ancestry controls NA Illumina [185250] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085382 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sildenafil 914 European ancestry cases, 319,844 European ancestry controls NA Affymetrix, Illumina [447990] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078202 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.1: Patient's noncompliance with medical treatment and regimen (Gene-based burden) 1,566 European ancestry cases, 382,234 European ancestry controls NA Illumina [185304] 0 medication adherence behavior http://www.ebi.ac.uk/efo/EFO_0006344 GCST90085384 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tadalafil 574 European ancestry cases, 320,184 European ancestry controls NA Affymetrix, Illumina [447990] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078221 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.14: Patient's other noncompliance with medication regimen (Gene-based burden) 736 European ancestry cases, 383,296 European ancestry controls NA Illumina [185305] 0 medication adherence behavior http://www.ebi.ac.uk/efo/EFO_0006344 GCST90085383 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mirena 24hrs intrauterine system 674 European ancestry cases, 320,084 European ancestry controls NA Affymetrix, Illumina [447989] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078154 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.5: Personal history of self-harm (Gene-based burden) 1,490 European ancestry cases, 386,331 European ancestry controls NA Illumina [185338] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085385 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin b6 preparation 517 European ancestry cases, 320,241 European ancestry controls NA Affymetrix, Illumina [447989] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078140 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.6: Personal history of other physical trauma (Gene-based burden) 726 European ancestry cases, 387,204 European ancestry controls NA Illumina [185344] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085386 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tamsulosin 4,522 European ancestry cases, 316,236 European ancestry controls NA Affymetrix, Illumina [447985] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078169 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.8: Other specified personal risk factors, not elsewhere classified (Gene-based burden) 5,202 European ancestry cases, 364,578 European ancestry controls NA Illumina [185056] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90085388 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - thiamine preparation 621 European ancestry cases, 320,137 European ancestry controls NA Affymetrix, Illumina [447983] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078124 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.89: Other specified personal risk factors, not elsewhere classified (Gene-based burden) 5,122 European ancestry cases, 364,657 European ancestry controls NA Illumina [185056] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90085387 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - 2 to 3 times a week (UKB data field 20414) 41,974 European ancestry cases, 97,568 European ancestry controls NA Affymetrix, Illumina [241043] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078429 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35: polymyalgia rheumatica (Gene-based burden) 908 European ancestry cases, 328,144 European ancestry controls NA Illumina [184145] 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90081795 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - 4 or more times a week (UKB data field 20414) 42,676 European ancestry cases, 96,866 European ancestry controls NA Affymetrix, Illumina [241043] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078430 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Post natal depression (Gene-based burden) 547 European ancestry cases, 331,207 European ancestry controls NA Illumina [184201] 0 postpartum depression http://www.ebi.ac.uk/efo/EFO_0007453 GCST90081906 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had known person concerned about or recommend reduction of alcohol consumption but not in the last year (UKB data field 20405) 6,352 European ancestry cases, 133,151 European ancestry controls NA Affymetrix, Illumina [241038] 0 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST90078403 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prolapsed disc or slipped disc (Gene-based burden) 7,846 European ancestry cases, 323,908 European ancestry controls NA Illumina [184201] 0 vertebral joint disease http://www.ebi.ac.uk/efo/EFO_0009477 GCST90081769 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had known person concerned about or recommend reduction of alcohol consumption during the last year (UKB data field 20405) 5,724 European ancestry cases, 133,779 European ancestry controls NA Affymetrix, Illumina [241038] 0 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST90078404 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51: Prolapsed disc or slipped disc (Gene-based burden) 6,808 European ancestry cases, 322,244 European ancestry controls NA Illumina [184145] 0 vertebral joint disease http://www.ebi.ac.uk/efo/EFO_0009477 GCST90081770 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - kliovance 929 European ancestry cases, 319,829 European ancestry controls NA Affymetrix, Illumina [445640] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078198 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.3: Colostomy status (Gene-based burden) 1,243 European ancestry cases, 386,672 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085400 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - alfuzosin 1,052 European ancestry cases, 319,706 European ancestry controls NA Affymetrix, Illumina [443121] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078092 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.6: Other artificial openings of urinary tract status (Gene-based burden) 543 European ancestry cases, 387,384 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085401 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - Every day (UKB data field 971) 40,526 European ancestry cases, 272,358 European ancestry controls NA Affymetrix, Illumina [440396] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079524 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z94: Transplanted organ and tissue status (Gene-based burden) 1,305 European ancestry cases, 386,601 European ancestry controls NA Illumina [185344] 0 transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005198 GCST90085404 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - Once a week (UKB data field 971) 59,744 European ancestry cases, 253,140 European ancestry controls NA Affymetrix, Illumina [440396] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079521 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z94.8: Other transplanted organ and tissue status (Gene-based burden) 513 European ancestry cases, 387,414 European ancestry controls NA Illumina [185344] 0 transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005198 GCST90085403 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - Once in the last 4 weeks (UKB data field 971) 25,277 European ancestry cases, 287,607 European ancestry controls NA Affymetrix, Illumina [440396] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079519 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95: Presence of cardiac and vascular implants and grafts (Gene-based burden) 16,113 European ancestry cases, 371,682 European ancestry controls NA Illumina [185339] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085411 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - 2 to 3 times in the last 4 weeks (UKB data field 971) 95,935 European ancestry cases, 216,949 European ancestry controls NA Affymetrix, Illumina [440396] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079520 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.0: Presence of cardiac pacemaker (Gene-based burden) 3,224 European ancestry cases, 384,575 European ancestry controls NA Illumina [185338] 0 artificial cardiac pacemaker http://www.ebi.ac.uk/efo/EFO_0009719 GCST90085405 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - 2 to 3 times a week (UKB data field 971) 77,785 European ancestry cases, 235,099 European ancestry controls NA Affymetrix, Illumina [440396] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079522 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.1: Presence of aortocoronary bypass graft (Gene-based burden) 5,314 European ancestry cases, 382,605 European ancestry controls NA Illumina [185344] 0 coronary artery bypass http://www.ebi.ac.uk/efo/EFO_0003776 GCST90085406 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - 4 to 5 times a week (UKB data field 971) 38,670 European ancestry cases, 274,214 European ancestry controls NA Affymetrix, Illumina [440396] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079523 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.2: Presence of prosthetic heart valve (Gene-based burden) 1,244 European ancestry cases, 386,684 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085407 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 15 and 30 minutes (UKB data field 981) 69,233 European ancestry cases, 243,544 European ancestry controls NA Affymetrix, Illumina [440320] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079526 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.4: Presence of other heart-valve replacement (Gene-based burden) 1,277 European ancestry cases, 386,650 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085408 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Less than 15 minutes (UKB data field 981) 5,397 European ancestry cases, 307,380 European ancestry controls NA Affymetrix, Illumina [440320] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079525 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.5: Presence of coronary angioplasty implant and graft (Gene-based burden) 7,744 European ancestry cases, 380,175 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085409 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 30 minutes and 1 hour (UKB data field 981) 121,322 European ancestry cases, 191,455 European ancestry controls NA Affymetrix, Illumina [440320] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079527 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.8: Presence of other cardiac and vascular implants and grafts (Gene-based burden) 2,644 European ancestry cases, 385,255 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085410 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 1 and 1.5 hours (UKB data field 981) 62,226 European ancestry cases, 250,551 European ancestry controls NA Affymetrix, Illumina [440320] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079528 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96: Presence of other functional implants (Gene-based burden) 24,749 European ancestry cases, 362,524 European ancestry controls NA Illumina [185330] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085416 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 1 5 and 2 hours (UKB data field 981) 31,911 European ancestry cases, 280,866 European ancestry controls NA Affymetrix, Illumina [440320] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079529 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - xalatan eye drops 1,232 European ancestry cases, 319,526 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078177 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.1: Allergy status to other antibiotic agents status (Gene-based burden) 4,694 European ancestry cases, 382,684 European ancestry controls NA Illumina [185338] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085368 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - zinc product 3,068 European ancestry cases, 317,690 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078127 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.2: Allergy status to sulfonamides status (Gene-based burden) 1,038 European ancestry cases, 386,819 European ancestry controls NA Illumina [185341] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085369 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - zopiclone 1,528 European ancestry cases, 319,230 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078021 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.5: Allergy status to narcotic agent status (Gene-based burden) 1,709 European ancestry cases, 386,221 European ancestry controls NA Illumina [185344] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085370 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - betamethasone 727 European ancestry cases, 320,031 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078073 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.6: Allergy status to analgesic agent status (Gene-based burden) 5,809 European ancestry cases, 381,836 European ancestry controls NA Illumina [185344] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085371 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - elleste solo 783 European ancestry cases, 319,975 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078164 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.8: Allergy status to other drugs, medicaments and biological substances status (Gene-based burden) 7,086 European ancestry cases, 380,334 European ancestry controls NA Illumina [185333] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085372 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fenofibrate 614 European ancestry cases, 320,144 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078008 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.9: Allergy status to unspecified drugs, medicaments and biological substances status (Gene-based burden) 4,483 European ancestry cases, 372,028 European ancestry controls NA Illumina [185157] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085373 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - isosorbide mononitrate 1,481 European ancestry cases, 319,277 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078001 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z89: Acquired absence of limb (Gene-based burden) 626 European ancestry cases, 387,200 European ancestry controls NA Illumina [185339] 0 amputation http://www.ebi.ac.uk/efo/EFO_0009632 GCST90085375 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mesalazine 645 European ancestry cases, 320,113 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078030 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90: Acquired absence of organs, not elsewhere classified (Gene-based burden) 20,599 European ancestry cases, 364,959 European ancestry controls NA Illumina [185324] 0 organ extraction http://www.ebi.ac.uk/efo/EFO_0009124 GCST90085381 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - minerals magnesium 1,035 European ancestry cases, 319,723 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078174 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.1: Acquired absence of breast and nipple (Gene-based burden) 3,153 European ancestry cases, 384,776 European ancestry controls NA Illumina [185344] 0 mastectomy http://www.ebi.ac.uk/efo/EFO_0020987 GCST90085376 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pizotifen 662 European ancestry cases, 320,096 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078111 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.2: Acquired absence of lung [part of] (Gene-based burden) 757 European ancestry cases, 387,171 European ancestry controls NA Illumina [185344] 0 lung transplantation http://www.ebi.ac.uk/efo/EFO_0010721 GCST90085377 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tranexamic acid 568 European ancestry cases, 320,190 European ancestry controls NA Affymetrix, Illumina [447991] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078007 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.4: Acquired absence of other specified parts of digestive tract (Gene-based burden) 8,508 European ancestry cases, 379,347 European ancestry controls NA Illumina [185344] 0 digestive system surgery http://www.ebi.ac.uk/efo/EFO_0020979 GCST90085378 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - co-tenidone 615 European ancestry cases, 320,143 European ancestry controls NA Affymetrix, Illumina [447990] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078160 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.5: Acquired absence of kidney (Gene-based burden) 1,507 European ancestry cases, 386,407 European ancestry controls NA Illumina [185344] 0 organ extraction http://www.ebi.ac.uk/efo/EFO_0009124 GCST90085379 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - finasteride 1,878 European ancestry cases, 318,880 European ancestry controls NA Affymetrix, Illumina [447990] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078048 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent lack of interest or pleasure in doing things - Nearly every day (UKB data field 20514) 2,264 European ancestry cases, 137,088 European ancestry controls NA Affymetrix, Illumina [240821] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078591 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D86: sarcoidosis (Gene-based burden) 746 European ancestry cases, 328,306 European ancestry controls NA Illumina [184145] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90081791 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent lack of interest or pleasure in doing things - Several days (UKB data field 20514) 21,161 European ancestry cases, 118,191 European ancestry controls NA Affymetrix, Illumina [240821] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078589 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tibolone 768 European ancestry cases, 319,990 European ancestry controls NA Affymetrix, Illumina [447952] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078047 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92: Personal history of medical treatment (Gene-based burden) 42,783 European ancestry cases, 336,594 European ancestry controls NA Illumina [185179] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085397 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - cerazette 1,103 European ancestry cases, 319,655 European ancestry controls NA Affymetrix, Illumina [447931] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078220 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.1: Personal history of long-term (current) use of anticoagulants (Gene-based burden) 15,024 European ancestry cases, 372,906 European ancestry controls NA Illumina [185344] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085390 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - premarin 1,836 European ancestry cases, 318,922 European ancestry controls NA Affymetrix, Illumina [447768] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078045 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.2: Personal history of drug therapy (Gene-based burden) 23,381 European ancestry cases, 357,348 European ancestry controls NA Illumina [185208] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085392 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - elleste duet conti 927 European ancestry cases, 319,831 European ancestry controls NA Affymetrix, Illumina [447708] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078186 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.29: Personal history of other drug therapy (Gene-based burden) 1,706 European ancestry cases, 379,051 European ancestry controls NA Illumina [185208] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085391 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evorel conti patch 528 European ancestry cases, 320,230 European ancestry controls NA Affymetrix, Illumina [447664] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078182 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.3: Personal history of irradiation (Gene-based burden) 4,774 European ancestry cases, 383,155 European ancestry controls NA Illumina [185344] 0 radiation exposure http://www.ebi.ac.uk/efo/EFO_0020980 GCST90085393 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prempak 647 European ancestry cases, 320,111 European ancestry controls NA Affymetrix, Illumina [447658] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90077997 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.4: Personal history of major surgery, not elsewhere classified (Gene-based burden) 1,702 European ancestry cases, 386,228 European ancestry controls NA Illumina [185344] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085394 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - livial 594 European ancestry cases, 320,164 European ancestry controls NA Affymetrix, Illumina [447610] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078105 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.6: Personal history of chemotherapy for neoplastic disease (Gene-based burden) 4,641 European ancestry cases, 383,289 European ancestry controls NA Illumina [185344] 0 neoplastic disease or syndrome http://purl.obolibrary.org/obo/MONDO_0023370 GCST90085395 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - estraderm mx 25 patch 666 European ancestry cases, 320,092 European ancestry controls NA Affymetrix, Illumina [447540] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078166 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.8: Personal history of other medical treatment (Gene-based burden) 722 European ancestry cases, 385,465 European ancestry controls NA Illumina [185314] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90085396 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - femoston 712 European ancestry cases, 320,046 European ancestry controls NA Affymetrix, Illumina [447516] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078157 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93: Artificial opening status (Gene-based burden) 3,783 European ancestry cases, 384,080 European ancestry controls NA Illumina [185343] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085402 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vagifem pessary 1,431 European ancestry cases, 319,327 European ancestry controls NA Affymetrix, Illumina [447470] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078046 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.1: Gastrostomy status (Gene-based burden) 583 European ancestry cases, 387,340 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085398 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - premique 866 European ancestry cases, 319,892 European ancestry controls NA Affymetrix, Illumina [446970] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078158 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.2: Ileostomy status (Gene-based burden) 1,429 European ancestry cases, 386,458 European ancestry controls NA Illumina [185341] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085399 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.1: Excessive and frequent menstruation with irregular cycle 2,965 European ancestry cases, 208,899 European ancestry controls NA Affymetrix, Illumina [332075] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90080685 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when walking normally (UKB data field 5485) (Gene-based burden) 22,256 European ancestry cases, 17,177 European ancestry controls NA Illumina [135405] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083339 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O70: Perineal laceration during delivery 5,700 European ancestry cases, 206,171 European ancestry controls NA Affymetrix, Illumina [332074] 0 perineal laceration during delivery http://www.ebi.ac.uk/efo/EFO_0009816 GCST90080735 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when walking uphill or hurrying (UKB data field 5474) (Gene-based burden) 26,456 European ancestry cases, 12,452 European ancestry controls NA Illumina [134945] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083338 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O36: Maternal care for other fetal problems 2,007 European ancestry cases, 209,824 European ancestry controls NA Affymetrix, Illumina [332046] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080716 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg predicted mass left (UKB data field 23118) (Gene-based burden) 423,618 European ancestry individuals NA Illumina [185869] 0 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90082907 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O26: Maternal care for other conditions predominantly related to pregnancy 1,939 European ancestry cases, 209,902 European ancestry controls NA Affymetrix, Illumina [332020] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080711 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg predicted mass right (UKB data field 23114) (Gene-based burden) 423,649 European ancestry individuals NA Illumina [185869] 0 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90082903 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O13: Gestational [pregnancy-induced] hypertension without significant proteinuria 501 European ancestry cases, 211,311 European ancestry controls NA Affymetrix, Illumina [332012] 0 preeclampsia, Proteinuria http://www.ebi.ac.uk/efo/EFO_0000668, http://purl.obolibrary.org/obo/HP_0000093 GCST90080708 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Length of longest manic irritable episode - At least two days but less than a week (UKB data field 5663) (Gene-based burden) 17,754 European ancestry cases, 11,089 European ancestry controls NA Illumina [124028] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083353 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O42.9: Premature rupture of membranes, unspecified as to length of time between rupture and onset of labor 566 European ancestry cases, 211,437 European ancestry controls NA Affymetrix, Illumina [331976] 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90080717 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Length of longest manic irritable episode - Less than a week (UKB data field 5663) (Gene-based burden) 5,617 European ancestry cases, 23,226 European ancestry controls NA Illumina [124028] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083354 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.9: Endometriosis, unspecified 840 European ancestry cases, 210,931 European ancestry controls NA Affymetrix, Illumina [331960] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90080651 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Length of longest manic irritable episode - A week or more (UKB data field 5663) (Gene-based burden) 6,072 European ancestry cases, 22,771 European ancestry controls NA Illumina [124028] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083355 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.9: Leiomyoma of uterus, unspecified 8,919 European ancestry cases, 202,851 European ancestry controls NA Affymetrix, Illumina [331959] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90079688 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 500 Never (UKB data field 21030) (Gene-based burden) 49,036 European ancestry cases, 34,033 European ancestry controls NA Illumina [159568] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082693 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O32: Maternal care for malpresentation of fetus 1,201 European ancestry cases, 210,543 European ancestry controls NA Affymetrix, Illumina [331932] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080712 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 501 Sometimes (UKB data field 21030) (Gene-based burden) 24,863 European ancestry cases, 58,206 European ancestry controls NA Illumina [159568] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082694 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C54: Malignant neoplasm of corpus uteri 1,515 European ancestry cases, 210,164 European ancestry controls 1,141 European ancestry cases, 122,694 European ancestry controls Affymetrix, Illumina [331863] 0 uterine corpus cancer http://www.ebi.ac.uk/efo/EFO_0007532 GCST90079608 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 502 Often (UKB data field 21030) (Gene-based burden) 3,613 European ancestry cases, 79,456 European ancestry controls NA Illumina [159568] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082695 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C56: Malignant neoplasm of ovary 1,188 European ancestry cases, 210,464 European ancestry controls 460 European ancestry cases, 122,719 European ancestry controls Affymetrix, Illumina [331832] 0 ovarian neoplasm http://www.ebi.ac.uk/efo/EFO_0003893 GCST90079609 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 503 Most of the time (UKB data field 21030) (Gene-based burden) 4,053 European ancestry cases, 79,016 European ancestry controls NA Illumina [159568] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082696 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N70: Salpingitis and oophoritis 618 European ancestry cases, 211,035 European ancestry controls NA Affymetrix, Illumina [331825] 0 Pelvic Inflammatory Disease http://www.ebi.ac.uk/efo/EFO_1001388 GCST90080642 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 504 Always (UKB data field 21030) (Gene-based burden) 1,504 European ancestry cases, 81,565 European ancestry controls NA Illumina [159568] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082697 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O72: Postpartum hemorrhage 1,418 European ancestry cases, 210,220 European ancestry controls NA Affymetrix, Illumina [331803] 0 postpartum hemorrhage http://www.ebi.ac.uk/efo/EFO_0009579 GCST90080737 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interpolated Age of participant when non cancer illness first diagnosed (UKB data field 20009) (Gene-based burden) 331,753 European ancestry individuals NA Illumina [184201] 0 age at onset, disease http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0000408 GCST90082228 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O47.1: False labor at or after 37 completed weeks of gestation 703 European ancestry cases, 228,431 European ancestry controls NA Affymetrix, Illumina [351970] 0 Braxton-Hicks contractions http://www.ebi.ac.uk/efo/EFO_0009639 GCST90080721 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interpolated Age of participant when operation took place (UKB data field 20011) (Gene-based burden) 346,023 European ancestry individuals NA Illumina [184584] 0 medical procedure, age at onset http://www.ebi.ac.uk/efo/EFO_0002571, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90082230 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O72.1: Other immediate postpartum hemorrhage 1,046 European ancestry cases, 228,088 European ancestry controls NA Affymetrix, Illumina [351967] 0 postpartum hemorrhage http://www.ebi.ac.uk/efo/EFO_0009579 GCST90080736 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interval between previous point and current one in alphanumeric path trail 2 (UKB data field 20155) (Gene-based burden) 98,260 European ancestry individuals NA Illumina [164035] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082307 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O80.0: Spontaneous vertex delivery 1,665 European ancestry cases, 227,469 European ancestry controls NA Affymetrix, Illumina [351963] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080739 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interval between previous point and current one in numeric path trail 1 (UKB data field 20149) (Gene-based burden) 102,460 European ancestry individuals NA Illumina [165155] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082301 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O63.1: Prolonged second stage (of labor) 1,487 European ancestry cases, 227,647 European ancestry controls NA Affymetrix, Illumina [351955] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90080725 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure corneal compensated left (UKB data field 5262) (Gene-based burden) 105,697 European ancestry individuals NA Illumina [167144] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90083323 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C54.1: Malignant neoplasm of endometrium 1,469 European ancestry cases, 227,317 European ancestry controls 744 European ancestry cases, 122,694 European ancestry controls Affymetrix, Illumina [351606] 0 endometrial cancer http://purl.obolibrary.org/obo/MONDO_0011962 GCST90079607 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure corneal compensated right (UKB data field 5254) (Gene-based burden) 105,888 European ancestry individuals NA Illumina [167136] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90083319 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bleed 49,682 European ancestry cases, 178,676 European ancestry controls NA Affymetrix, Illumina [351295] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90081519 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure Goldmann correlated left (UKB data field 5263) (Gene-based burden) 105,697 European ancestry individuals NA Illumina [167144] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90083324 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z35: Supervision of high-risk pregnancy 1,111 European ancestry cases, 228,023 European ancestry controls NA Affymetrix, Illumina [350934] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081246 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure Goldmann correlated right (UKB data field 5255) (Gene-based burden) 105,888 European ancestry individuals NA Illumina [167136] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90083320 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O34.2: Maternal care due to uterine scar from previous surgery 1,286 European ancestry cases, 227,848 European ancestry controls NA Affymetrix, Illumina [349480] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080713 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Physical activity group - high (UKB data field 22032) (Gene-based burden) 141,453 European ancestry cases, 207,940 European ancestry controls NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082839 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism - composite 5,702 European ancestry cases, 220,211 European ancestry controls NA Affymetrix, Illumina [348468] 0 venous thromboembolism, deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0003907 GCST90081534 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Physical activity group - low (UKB data field 22032) (Gene-based burden) 65,285 European ancestry cases, 284,108 European ancestry controls NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082837 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O99.0: Anemia complicating pregnancy, childbirth and the puerperium 922 European ancestry cases, 228,212 European ancestry controls NA Affymetrix, Illumina [347514] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90080741 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Physical activity group - moderate (UKB data field 22032) (Gene-based burden) 142,655 European ancestry cases, 206,738 European ancestry controls NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082838 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism / Deep vein thrombosis 591 European ancestry cases, 220,210 European ancestry controls NA Affymetrix, Illumina [342484] 0 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90081535 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Irritability (UKB data field 1940) (Gene-based burden) 120,504 European ancestry cases, 292,618 European ancestry controls NA Illumina [185721] 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90081606 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.8: Other noninflammatory disorders of ovary, fallopian tube and broad ligament 611 European ancestry cases, 211,393 European ancestry controls NA Affymetrix, Illumina [332236] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080662 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ischemic stroke or cardioembolic stroke (Gene-based burden) 2,793 European ancestry cases, 256,694 European ancestry controls NA Illumina [181955] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90085478 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.0: Endometrial hyperplasia 1,071 European ancestry cases, 210,928 European ancestry controls NA Affymetrix, Illumina [332230] 0 obsolete endometrial hyperplasia http://purl.obolibrary.org/obo/MONDO_0041161 GCST90080667 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 1 (UKB data field 6332) (Gene-based burden) 8,910 European ancestry cases, 15,529 European ancestry controls NA Illumina [113488] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083483 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N87.0: Mild cervical dysplasia 665 European ancestry cases, 211,333 European ancestry controls NA Affymetrix, Illumina [332228] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90080672 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 2 (UKB data field 6332) (Gene-based burden) 23,214 European ancestry cases, 1,225 European ancestry controls NA Illumina [113488] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083484 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N90.8: Other specified noninflammatory disorders of vulva and perineum 706 European ancestry cases, 211,293 European ancestry controls NA Affymetrix, Illumina [332228] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080681 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 4 (UKB data field 6332) (Gene-based burden) 8,674 European ancestry cases, 15,765 European ancestry controls NA Illumina [113488] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083485 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O03.9: Complete or unspecified spontaneous abortion without complication 664 European ancestry cases, 211,333 European ancestry controls NA Affymetrix, Illumina [332225] 0 abortion http://www.ebi.ac.uk/efo/EFO_1001491 GCST90080706 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 6 (UKB data field 6332) (Gene-based burden) 14,457 European ancestry cases, 9,982 European ancestry controls NA Illumina [113488] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083486 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.2: Incomplete uterovaginal prolapse 4,359 European ancestry cases, 207,635 European ancestry controls NA Affymetrix, Illumina [332222] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080654 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 7 (UKB data field 6332) (Gene-based burden) 20,635 European ancestry cases, 3,804 European ancestry controls NA Illumina [113488] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083487 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.4: Malposition of uterus 872 European ancestry cases, 211,111 European ancestry controls NA Affymetrix, Illumina [332220] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080669 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - top left (UKB data field 6332) (Gene-based burden) 23,512 European ancestry cases, 927 European ancestry controls NA Illumina [113488] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083482 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84.0: Polyp of corpus uteri 8,912 European ancestry cases, 203,081 European ancestry controls NA Affymetrix, Illumina [332219] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90080664 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Human Polyomavirus JCV (UKB data field 23066) (Gene-based burden) 4,863 European ancestry cases, 3,678 European ancestry controls NA Illumina [70714] 0 polyomavirus 2 seropositivity http://www.ebi.ac.uk/efo/EFO_0010907 GCST90082880 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O63: Long labor 2,057 European ancestry cases, 209,943 European ancestry controls NA Affymetrix, Illumina [332215] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90080726 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Keyed up or on edge during worst period of anxiety (UKB data field 20423) (Gene-based burden) 32,732 European ancestry cases, 8,568 European ancestry controls NA Illumina [136171] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90082427 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O36.8: Maternal care for other specified fetal problems 1,084 European ancestry cases, 210,917 European ancestry controls NA Affymetrix, Illumina [332210] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080715 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Knee pain for three months (UKB data field 3773) (Gene-based burden) 76,543 European ancestry cases, 20,879 European ancestry controls NA Illumina [163757] 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90083059 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O42: Premature rupture of membranes 1,136 European ancestry cases, 210,861 European ancestry controls NA Affymetrix, Illumina [332208] 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90080718 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Direct low density lipoprotein levels (UKB data field 30780) (Gene-based burden) 411,351 European ancestry individuals NA Illumina [185659] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90083019 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.0: Excessive and frequent menstruation with regular cycle 9,262 European ancestry cases, 202,718 European ancestry controls NA Affymetrix, Illumina [332204] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90080684 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat free mass left (UKB data field 23117) (Gene-based burden) 423,624 European ancestry individuals NA Illumina [185869] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90082906 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N88.8: Other specified noninflammatory disorders of cervix uteri 1,130 European ancestry cases, 210,838 European ancestry controls NA Affymetrix, Illumina [332202] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080676 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat free mass right (UKB data field 23113) (Gene-based burden) 423,650 European ancestry individuals NA Illumina [185869] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90082902 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O46.9: Antepartum hemorrhage, unspecified 639 European ancestry cases, 211,333 European ancestry controls NA Affymetrix, Illumina [332195] 0 Antepartum hemorrhage http://purl.obolibrary.org/obo/HP_0025328 GCST90080719 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat mass left (UKB data field 23116) (Gene-based burden) 423,640 European ancestry individuals NA Illumina [185869] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90082905 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N87.9: Dysplasia of cervix uteri, unspecified 527 European ancestry cases, 211,441 European ancestry controls NA Affymetrix, Illumina [332193] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90080673 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat mass right (UKB data field 23112) (Gene-based burden) 423,659 European ancestry individuals NA Illumina [185869] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90082901 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O70.0: First degree perineal laceration during delivery 2,364 European ancestry cases, 209,629 European ancestry controls NA Affymetrix, Illumina [332191] 0 perineal laceration during delivery http://www.ebi.ac.uk/efo/EFO_0009816 GCST90080733 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat percentage left (UKB data field 23115) (Gene-based burden) 423,643 European ancestry individuals NA Illumina [185869] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90082904 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.8: Other specified noninflammatory disorders of uterus 2,734 European ancestry cases, 209,232 European ancestry controls NA Affymetrix, Illumina [332190] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080670 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat percentage right (UKB data field 23111) (Gene-based burden) 423,666 European ancestry individuals NA Illumina [185869] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90082900 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O47: False labor 1,135 European ancestry cases, 210,857 European ancestry controls NA Affymetrix, Illumina [332184] 0 Braxton-Hicks contractions http://www.ebi.ac.uk/efo/EFO_0009639 GCST90080722 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain in calf/calves (UKB data field 5463) (Gene-based burden) 12,782 European ancestry cases, 27,015 European ancestry controls NA Illumina [135644] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083337 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O46: Antepartum hemorrhage, not elsewhere classified 680 European ancestry cases, 211,264 European ancestry controls NA Affymetrix, Illumina [332167] 0 Antepartum hemorrhage http://purl.obolibrary.org/obo/HP_0025328 GCST90080720 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking (UKB data field 4728) (Gene-based burden) 40,481 European ancestry cases, 135,686 European ancestry controls NA Illumina [177018] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083204 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N62: Hypertrophy of breast 707 European ancestry cases, 211,231 European ancestry controls NA Affymetrix, Illumina [332165] 0 Breast hypertrophy http://purl.obolibrary.org/obo/HP_0010313 GCST90080640 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - action taken - Continue at same pace (UKB data field 5507) (Gene-based burden) 13,792 European ancestry cases, 26,027 European ancestry controls NA Illumina [135888] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083343 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O34: Maternal care for abnormality of pelvic organs 1,615 European ancestry cases, 210,342 European ancestry controls NA Affymetrix, Illumina [332161] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080714 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - action taken - Slow down (UKB data field 5507) (Gene-based burden) 20,708 European ancestry cases, 19,111 European ancestry controls NA Illumina [135888] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083342 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z37.0: Single live birth 11,980 European ancestry cases, 199,928 European ancestry controls NA Affymetrix, Illumina [332136] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90081249 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - action taken - Stop (UKB data field 5507) (Gene-based burden) 6,007 European ancestry cases, 33,812 European ancestry controls NA Illumina [135888] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083341 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O03.4: Incomplete spontaneous abortion without complication 797 European ancestry cases, 211,109 European ancestry controls NA Affymetrix, Illumina [332125] 0 incomplete abortion http://www.ebi.ac.uk/efo/EFO_1001799 GCST90080705 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - effect of standing still - Pain usually continues for more than 10 minutes (UKB data field 5518) (Gene-based burden) 13,520 European ancestry cases, 21,601 European ancestry controls NA Illumina [130894] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083344 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O60: Preterm labor 690 European ancestry cases, 211,192 European ancestry controls NA Affymetrix, Illumina [332102] 0 premature birth http://www.ebi.ac.uk/efo/EFO_0003917 GCST90080724 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - effect of standing still - Pain usually disappears in less than 10 minutes (UKB data field 5518) (Gene-based burden) 22,075 European ancestry cases, 13,046 European ancestry controls NA Illumina [130894] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083345 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N93.0: Postcoital and contact bleeding 1,256 European ancestry cases, 210,631 European ancestry controls NA Affymetrix, Illumina [332101] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90080689 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when standing still or sitting (UKB data field 5452) (Gene-based burden) 24,490 European ancestry cases, 14,717 European ancestry controls NA Illumina [135188] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083336 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D27: Benign neoplasm of ovary 1,704 European ancestry cases, 210,162 European ancestry controls NA Affymetrix, Illumina [332080] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079690 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when walking ever disappears while walking (UKB data field 5496) (Gene-based burden) 7,982 European ancestry cases, 13,580 European ancestry controls NA Illumina [110933] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90083340 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Lung cancer (UKB data field 20107) (Gene-based burden) 35,172 European ancestry cases, 384,425 European ancestry controls NA Illumina [185792] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082245 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maternal age at death (UKB data field 3526) 263,428 European ancestry individuals NA Affymetrix, Illumina [387793] 0 mother's age at death http://www.ebi.ac.uk/efo/EFO_0009721 GCST90079060 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Stroke (UKB data field 20107) (Gene-based burden) 60,161 European ancestry cases, 359,437 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082244 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ischemic stroke or cardioembolic stroke 2,793 European ancestry cases, 256,694 European ancestry controls NA Affymetrix, Illumina [385814] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90081492 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Alzheimers disease dementia (UKB data field 20107) (Gene-based burden) 20,299 European ancestry cases, 399,299 European ancestry controls NA Illumina [185792] 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90082239 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Birth weight (UKB data field 20022) 247,016 European ancestry individuals NA Affymetrix, Illumina [373133] 2 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90078251 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Parkinsons disease (UKB data field 20107) (Gene-based burden) 9,552 European ancestry cases, 410,045 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082240 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Obesity 104,086 European ancestry cases, 142,553 European ancestry controls NA Affymetrix, Illumina [372704] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90081522 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Severe depression (UKB data field 20107) (Gene-based burden) 14,714 European ancestry cases, 404,883 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082241 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankle spacing width (UKB data field 3143) 246,319 European ancestry individuals NA Affymetrix, Illumina [370341] 1 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90079048 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Prostate cancer (UKB data field 20107) (Gene-based burden) 29,430 European ancestry cases, 390,167 European ancestry controls NA Illumina [185792] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082242 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density T score automated (UKB data field 78) 246,319 European ancestry individuals NA Affymetrix, Illumina [370341] 1 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90079502 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 11 Do not know group 1 (UKB data field 20107) (Gene-based burden) 29,911 European ancestry cases, 389,687 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082250 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel quantitative ultrasound index direct entry (UKB data field 3147) 246,319 European ancestry individuals NA Affymetrix, Illumina [370341] 1 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90079051 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 17 None of the above group 1 (UKB data field 20107) (Gene-based burden) 142,509 European ancestry cases, 277,089 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082251 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of sound through heel (UKB data field 3146) 246,319 European ancestry individuals NA Affymetrix, Illumina [370341] 1 velocity of sound measurement http://www.ebi.ac.uk/efo/EFO_0005654 GCST90079050 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 21 Do not know group 2 (UKB data field 20107) (Gene-based burden) 34,809 European ancestry cases, 384,788 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082252 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel Broadband ultrasound attenuation direct entry (UKB data field 3144) 246,304 European ancestry individuals NA Affymetrix, Illumina [370332] 1 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90079049 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 27 None of the above group 2 (UKB data field 20107) (Gene-based burden) 284,370 European ancestry cases, 135,227 European ancestry controls NA Illumina [185792] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082253 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density (UKB data field 3148) 246,206 European ancestry individuals NA Affymetrix, Illumina [370211] 1 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90079052 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Alzheimers disease dementia (UKB data field 20110) (Gene-based burden) 38,659 European ancestry cases, 385,028 European ancestry controls NA Illumina [185841] 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90082255 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of vigorous activity (UKB data field 914) 242,729 European ancestry individuals NA Affymetrix, Illumina [367794] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079508 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - blood pressure (UKB data field 20110) (Gene-based burden) 125,109 European ancestry cases, 298,578 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082264 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had cervical smear test (UKB data field 2694) 228,394 European ancestry cases, 4,737 European ancestry controls NA Affymetrix, Illumina [357227] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90078956 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Bowel cancer (UKB data field 20110) (Gene-based burden) 20,783 European ancestry cases, 402,903 European ancestry controls NA Illumina [185841] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082261 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken oral contraceptive pill (UKB data field 2784) 191,547 European ancestry cases, 41,586 European ancestry controls NA Affymetrix, Illumina [357204] 0 contraception http://www.ebi.ac.uk/efo/EFO_0009520 GCST90078959 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Breast cancer (UKB data field 20110) (Gene-based burden) 33,019 European ancestry cases, 390,667 European ancestry controls NA Illumina [185841] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082262 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever used hormone replacement therapy (UKB data field 2814) 92,655 European ancestry cases, 140,348 European ancestry controls NA Affymetrix, Illumina [357104] 0 hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0003961 GCST90078962 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - cancer (UKB data field 20110) (Gene-based burden) 16,650 European ancestry cases, 407,036 European ancestry controls NA Illumina [185841] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082260 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had breast cancer screening mammogram (UKB data field 2674) 192,912 European ancestry cases, 40,420 European ancestry controls NA Affymetrix, Illumina [357046] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90078955 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Chronic bronchitis emphysema (UKB data field 20110) (Gene-based burden) 24,686 European ancestry cases, 399,001 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082263 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Had other major operations (UKB data field 2844) 157,226 European ancestry cases, 74,569 European ancestry controls NA Affymetrix, Illumina [355794] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90078964 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Diabetes (UKB data field 20110) (Gene-based burden) 38,129 European ancestry cases, 385,558 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082265 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism 10,941 European ancestry cases, 220,601 European ancestry controls NA Affymetrix, Illumina [354836] 1 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90081530 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Do not know group 1 (UKB data field 20110) (Gene-based burden) 17,882 European ancestry cases, 405,805 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082266 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bilateral oophorectomy (UKB data field 2834) 19,323 European ancestry cases, 211,189 European ancestry controls NA Affymetrix, Illumina [354257] 0 bilateral oophorectomy http://www.ebi.ac.uk/efo/EFO_0009717 GCST90078963 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Do not know group 2 (UKB data field 20110) (Gene-based burden) 21,332 European ancestry cases, 402,354 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082268 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.2: Malignant neoplasm of upper-inner quadrant of breast 775 European ancestry cases, 228,359 European ancestry controls NA Affymetrix, Illumina [351989] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079602 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Heart disease (UKB data field 20110) (Gene-based burden) 82,755 European ancestry cases, 340,932 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082258 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.4: Malignant neoplasm of upper-outer quadrant of breast 2,461 European ancestry cases, 226,673 European ancestry controls NA Affymetrix, Illumina [351989] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079603 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - None of the above group 1 (UKB data field 20110) (Gene-based burden) 167,918 European ancestry cases, 255,769 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082267 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.8: Malignant neoplasm of overlapping sites of breast 600 European ancestry cases, 228,534 European ancestry controls NA Affymetrix, Illumina [351989] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079604 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - None of the above group 2 (UKB data field 20110) (Gene-based burden) 308,506 European ancestry cases, 115,180 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082269 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D05.1: Intraductal carcinoma in situ of breast 1,447 European ancestry cases, 227,687 European ancestry controls NA Affymetrix, Illumina [351989] 0 intraductal breast neoplasm http://purl.obolibrary.org/obo/MONDO_0002488 GCST90079646 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Parkinsons disease (UKB data field 20110) (Gene-based burden) 6,625 European ancestry cases, 417,061 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082256 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D05.9: Unspecified type of carcinoma in situ of breast 1,072 European ancestry cases, 228,062 European ancestry controls NA Affymetrix, Illumina [351989] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90079647 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Severe depression (UKB data field 20110) (Gene-based burden) 26,963 European ancestry cases, 396,723 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082257 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D06.9: Carcinoma in situ of cervix, unspecified 569 European ancestry cases, 228,565 European ancestry controls NA Affymetrix, Illumina [351989] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90079649 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Stroke (UKB data field 20110) (Gene-based burden) 58,930 European ancestry cases, 364,757 European ancestry controls NA Illumina [185841] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082259 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.0: Submucous leiomyoma of uterus 1,413 European ancestry cases, 227,721 European ancestry controls NA Affymetrix, Illumina [351989] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90079685 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Bowel cancer (UKB data field 20111) (Gene-based burden) 9,037 European ancestry cases, 362,695 European ancestry controls NA Illumina [184937] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082277 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.1: Intramural leiomyoma of uterus 1,064 European ancestry cases, 228,070 European ancestry controls NA Affymetrix, Illumina [351989] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90079686 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Breast cancer (UKB data field 20111) (Gene-based burden) 16,443 European ancestry cases, 355,289 European ancestry controls NA Illumina [184937] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082278 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.2: Subserosal leiomyoma of uterus 755 European ancestry cases, 228,379 European ancestry controls NA Affymetrix, Illumina [351989] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90079687 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Chronic bronchitis emphysema (UKB data field 20111) (Gene-based burden) 10,430 European ancestry cases, 361,302 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082279 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N73.6: Female pelvic peritoneal adhesions (postinfective) 2,865 European ancestry cases, 226,269 European ancestry controls NA Affymetrix, Illumina [351989] 0 disease of peritoneum http://www.ebi.ac.uk/efo/EFO_0009541 GCST90080644 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Diabetes (UKB data field 20111) (Gene-based burden) 30,682 European ancestry cases, 341,050 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082281 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.0: Endometriosis of uterus 2,024 European ancestry cases, 227,110 European ancestry controls NA Affymetrix, Illumina [351989] 0 adenomyosis http://purl.obolibrary.org/obo/MONDO_0010888 GCST90080648 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Heart disease (UKB data field 20111) (Gene-based burden) 37,595 European ancestry cases, 334,137 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082274 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.1: Endometriosis of ovary 1,042 European ancestry cases, 228,092 European ancestry controls NA Affymetrix, Illumina [351989] 0 Ovarian Endometriosis http://www.ebi.ac.uk/efo/EFO_1000418 GCST90080649 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - High blood pressure (UKB data field 20111) (Gene-based burden) 75,991 European ancestry cases, 295,741 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082280 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.4: Uterovaginal prolapse, unspecified 1,373 European ancestry cases, 227,761 European ancestry controls NA Affymetrix, Illumina [351989] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080655 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Lung cancer (UKB data field 20111) (Gene-based burden) 8,284 European ancestry cases, 363,448 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082276 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.2: Hypertrophy of uterus 1,253 European ancestry cases, 227,881 European ancestry controls NA Affymetrix, Illumina [351989] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080668 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Stroke (UKB data field 20111) (Gene-based burden) 12,254 European ancestry cases, 359,478 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082275 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N90.7: Vulvar cyst 572 European ancestry cases, 228,562 European ancestry controls NA Affymetrix, Illumina [351989] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080680 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Alzheimers disease dementia (UKB data field 20111) (Gene-based burden) 2,512 European ancestry cases, 369,220 European ancestry controls NA Illumina [184937] 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90082270 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.3: Ovulation bleeding 997 European ancestry cases, 228,137 European ancestry controls NA Affymetrix, Illumina [351989] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080686 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Parkinsons disease (UKB data field 20111) (Gene-based burden) 2,119 European ancestry cases, 369,613 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082271 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95.0: Postmenopausal bleeding 10,065 European ancestry cases, 219,069 European ancestry controls NA Affymetrix, Illumina [351989] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080695 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Severe depression (UKB data field 20111) (Gene-based burden) 26,143 European ancestry cases, 345,589 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082272 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95.2: Postmenopausal atrophic vaginitis 1,317 European ancestry cases, 227,817 European ancestry controls NA Affymetrix, Illumina [351989] 0 postmenopausal atrophic vaginitis http://purl.obolibrary.org/obo/MONDO_0001410 GCST90080697 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Prostate cancer (UKB data field 20111) (Gene-based burden) 6,385 European ancestry cases, 365,347 European ancestry controls NA Illumina [184937] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90082273 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N99.3: Prolapse of vaginal vault after hysterectomy 565 European ancestry cases, 228,569 European ancestry controls NA Affymetrix, Illumina [351989] 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90080701 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 11 Do not know group 1 (UKB data field 20111) (Gene-based burden) 27,293 European ancestry cases, 344,439 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082282 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.1: Insertion of (intrauterine) contraceptive device 1,026 European ancestry cases, 228,108 European ancestry controls NA Affymetrix, Illumina [351989] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081234 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 17 None of the above group 1 (UKB data field 20111) (Gene-based burden) 231,453 European ancestry cases, 140,279 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082283 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.5: Surveillance of (intrauterine) contraceptive device 1,304 European ancestry cases, 227,830 European ancestry controls NA Affymetrix, Illumina [351989] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081239 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 21 Do not know group 2 (UKB data field 20111) (Gene-based burden) 27,290 European ancestry cases, 344,442 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082284 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.0: Follicular cyst of ovary 574 European ancestry cases, 228,560 European ancestry controls NA Affymetrix, Illumina [351988] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080659 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 27 None of the above group 2 (UKB data field 20111) (Gene-based burden) 290,729 European ancestry cases, 81,003 European ancestry controls NA Illumina [184937] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082285 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N88.2: Stricture and stenosis of cervix uteri 789 European ancestry cases, 228,345 European ancestry controls NA Affymetrix, Illumina [351988] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080675 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Immature reticulocyte fraction (UKB data field 30280) (Gene-based burden) 412,333 European ancestry individuals NA Illumina [185680] 0 reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0010700 GCST90082990 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.5: Vaginal enterocele 789 European ancestry cases, 228,345 European ancestry controls NA Affymetrix, Illumina [351986] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080656 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of arm left (UKB data field 23110) (Gene-based burden) 424,014 European ancestry individuals NA Illumina [185872] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90082899 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.1: Corpus luteum cyst 540 European ancestry cases, 228,594 European ancestry controls NA Affymetrix, Illumina [351981] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080660 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of arm right (UKB data field 23109) (Gene-based burden) 423,992 European ancestry individuals NA Illumina [185872] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90082898 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.3: Endometriosis of pelvic peritoneum 811 European ancestry cases, 228,323 European ancestry controls NA Affymetrix, Illumina [351980] 0 endometriosis of pelvic peritoneum http://purl.obolibrary.org/obo/MONDO_0001285 GCST90080650 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of leg left (UKB data field 23108) (Gene-based burden) 424,020 European ancestry individuals NA Illumina [185872] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90082897 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.2: Labour and delivery complicated by fetal heart rate anomaly with meconium in amniotic fluid 504 European ancestry cases, 228,630 European ancestry controls NA Affymetrix, Illumina [351980] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080729 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of leg right (UKB data field 23107) (Gene-based burden) 424,024 European ancestry individuals NA Illumina [185872] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90082896 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.8: Labour and delivery complicated by other evidence of fetal stress 539 European ancestry cases, 228,595 European ancestry controls NA Affymetrix, Illumina [351980] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080730 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of whole body (UKB data field 23106) (Gene-based burden) 424,003 European ancestry individuals NA Illumina [185870] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90082895 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68: Labor and delivery complicated by abnormality of fetal acid-base balance 3,526 European ancestry cases, 225,608 European ancestry controls NA Affymetrix, Illumina [351977] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080731 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Index of Multiple Deprivation England (UKB data field 26410) (Gene-based burden) 369,491 European ancestry individuals NA Illumina [185054] 0 Townsend deprivation index http://www.ebi.ac.uk/efo/EFO_0009711 GCST90082938 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.0: Labour and delivery complicated by fetal heart rate anomaly 1,408 European ancestry cases, 227,726 European ancestry controls NA Affymetrix, Illumina [351976] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080727 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Infectious illness diagnosis status when IBS symptoms first began (UKB data field 21071) (Gene-based burden) 1,871 European ancestry cases, 16,625 European ancestry controls NA Illumina [103255] 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90082821 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.1: Labour and delivery complicated by meconium in amniotic fluid 962 European ancestry cases, 228,172 European ancestry controls NA Affymetrix, Illumina [351972] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080728 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Insulin levels (UKB data field 6177) (Gene-based burden) 2,807 European ancestry cases, 66,666 European ancestry controls NA Illumina [153090] 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90083474 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O70.1: Second degree perineal laceration during delivery 3,499 European ancestry cases, 225,635 European ancestry controls NA Affymetrix, Illumina [351971] 0 perineal laceration during delivery http://www.ebi.ac.uk/efo/EFO_0009816 GCST90080734 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-09-27 33887147 Young WJ 2021-04-22 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33887147 Genetically-Determined Serum Calcium Levels and Markers of Ventricular Repolarisation: A Mendelian Randomization Study in the UK Biobank. Calcium levels 305,349 European ancestry individuals NA Affymetrix [NR] (imputed) 215 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST012398 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N89.8: Other specified noninflammatory disorders of vagina 1,410 European ancestry cases, 209,913 European ancestry controls NA Affymetrix, Illumina [331439] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080678 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of mania or irritability - At least a day but less than a week (UKB data field 20492) (Gene-based burden) 13,147 European ancestry cases, 20,128 European ancestry controls NA Illumina [128161] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082518 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O20: Hemorrhage in early pregnancy 1,083 European ancestry cases, 210,227 European ancestry controls NA Affymetrix, Illumina [331421] 0 hemorrhage http://purl.obolibrary.org/obo/MP_0001914 GCST90080710 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of mania or irritability - Less than 24 hours (UKB data field 20492) (Gene-based burden) 12,323 European ancestry cases, 20,952 European ancestry controls NA Illumina [128161] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082517 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D06: Carcinoma in situ of cervix uteri 665 European ancestry cases, 210,614 European ancestry controls NA Affymetrix, Illumina [331391] 0 uterine cervix carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0042487 GCST90079650 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of unenthusiasm/disinterest (UKB data field 5375) (Gene-based burden) 49,039 European ancestry individuals NA Illumina [143453] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90083330 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O99: Other maternal diseases classifiable elsewhere but complicating pregnancy, childbirth and the puerperium 2,035 European ancestry cases, 209,171 European ancestry controls NA Affymetrix, Illumina [331380] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90080743 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lymphocyte count (UKB data field 30120) (Gene-based burden) 418,449 European ancestry individuals NA Illumina [185795] 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90082977 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84.1: Polyp of cervix uteri 3,637 European ancestry cases, 207,539 European ancestry controls NA Affymetrix, Illumina [331303] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90080665 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lymphocyte percentage (UKB data field 30180) (Gene-based burden) 418,454 European ancestry individuals NA Illumina [185795] 0 lymphocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007993 GCST90082981 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z34: Encounter for supervision of normal pregnancy 2,526 European ancestry cases, 208,571 European ancestry controls NA Affymetrix, Illumina [331199] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081245 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I was more active than usual (UKB data field 6156) (Gene-based burden) 9,009 European ancestry cases, 26,424 European ancestry controls NA Illumina [132265] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083458 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E28: Ovarian dysfunction 500 European ancestry cases, 210,556 European ancestry controls NA Affymetrix, Illumina [331103] 0 ovarian dysfunction http://www.ebi.ac.uk/efo/EFO_0009003 GCST90079756 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I was more talkative than usual (UKB data field 6156) (Gene-based burden) 7,538 European ancestry cases, 27,895 European ancestry controls NA Illumina [132265] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083459 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z34.8: Encounter for supervision of other normal pregnancy 782 European ancestry cases, 210,963 European ancestry controls NA Affymetrix, Illumina [331100] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081243 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I needed less sleep than usual (UKB data field 6156) (Gene-based burden) 4,907 European ancestry cases, 30,526 European ancestry controls NA Illumina [132265] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083460 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.2: Other and unspecified ovarian cysts 4,400 European ancestry cases, 206,584 European ancestry controls NA Affymetrix, Illumina [331065] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080661 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I was more creative or had more ideas than usual (UKB data field 6156) (Gene-based burden) 4,295 European ancestry cases, 31,138 European ancestry controls NA Illumina [132265] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083461 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N75: Diseases of Bartholin's gland 988 European ancestry cases, 209,981 European ancestry controls NA Affymetrix, Illumina [331050] 0 Bartholin gland disease http://www.ebi.ac.uk/efo/EFO_0009469 GCST90080646 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - All of the above (UKB data field 6156) (Gene-based burden) 3,520 European ancestry cases, 31,913 European ancestry controls NA Illumina [132265] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083462 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O02: Other abnormal products of conception 1,470 European ancestry cases, 209,448 European ancestry controls NA Affymetrix, Illumina [330991] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080704 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - None of the above (UKB data field 6156) (Gene-based burden) 13,437 European ancestry cases, 21,996 European ancestry controls NA Illumina [132265] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083463 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.1: Cystocele 5,753 European ancestry cases, 205,179 European ancestry controls NA Affymetrix, Illumina [330933] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080653 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I needed less sleep than usual (UKB data field 20548) (Gene-based burden) 4,681 European ancestry cases, 20,639 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082641 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z37: Outcome of delivery 13,034 European ancestry cases, 197,840 European ancestry controls NA Affymetrix, Illumina [330913] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90081251 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was easily distracted (UKB data field 20548) (Gene-based burden) 11,129 European ancestry cases, 14,191 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082643 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O48: Late pregnancy 1,268 European ancestry cases, 210,715 European ancestry controls NA Affymetrix, Illumina [330888] 0 post term pregnancy http://www.ebi.ac.uk/efo/EFO_0009681 GCST90080723 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more active than usual (UKB data field 20548) (Gene-based burden) 6,975 European ancestry cases, 18,345 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082645 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94.8: Other specified conditions associated with female genital organs and menstrual cycle 1,042 European ancestry cases, 209,765 European ancestry controls NA Affymetrix, Illumina [330796] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080694 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more confident than usual (UKB data field 20548) (Gene-based burden) 4,064 European ancestry cases, 21,256 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082644 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N73: Other female pelvic inflammatory diseases 3,315 European ancestry cases, 207,461 European ancestry controls NA Affymetrix, Illumina [330782] 0 Pelvic Inflammatory Disease http://www.ebi.ac.uk/efo/EFO_1001388 GCST90080645 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more creative or had more ideas than usual (UKB data field 20548) (Gene-based burden) 3,827 European ancestry cases, 21,493 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082642 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94.1: Dyspareunia 1,397 European ancestry cases, 209,321 European ancestry controls NA Affymetrix, Illumina [330728] 0 Dyspareunia http://purl.obolibrary.org/obo/HP_0030016 GCST90080692 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more restless than usual (UKB data field 20548) (Gene-based burden) 15,465 European ancestry cases, 9,855 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082639 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50: Malignant neoplasm of breast 12,346 European ancestry cases, 198,242 European ancestry controls 3,449 European ancestry cases, 120,979 European ancestry controls Affymetrix, Illumina [330624] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90079606 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more talkative than usual (UKB data field 20548) (Gene-based burden) 6,709 European ancestry cases, 18,611 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082638 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N97.9: Female infertility, unspecified 1,163 European ancestry cases, 209,395 European ancestry controls NA Affymetrix, Illumina [330574] 0 female infertility http://www.ebi.ac.uk/efo/EFO_0008560 GCST90080699 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - My thoughts were racing (UKB data field 20548) (Gene-based burden) 12,782 European ancestry cases, 12,538 European ancestry controls NA Illumina [117332] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082640 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N86: Erosion and ectropion of cervix uteri 1,108 European ancestry cases, 209,282 European ancestry controls NA Affymetrix, Illumina [330371] 0 cervix erosion http://www.ebi.ac.uk/efo/EFO_1000862 GCST90080671 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Every day (UKB data field 20454) (Gene-based burden) 2,042 European ancestry cases, 27,933 European ancestry controls NA Illumina [124011] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90082465 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94.6: Dysmenorrhea, unspecified 1,843 European ancestry cases, 208,612 European ancestry controls NA Affymetrix, Illumina [330359] 0 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90080693 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Less than once a month (UKB data field 20454) (Gene-based burden) 19,420 European ancestry cases, 10,555 European ancestry controls NA Illumina [124011] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90082462 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.6: Irregular menstruation, unspecified 2,204 European ancestry cases, 208,273 European ancestry controls NA Affymetrix, Illumina [330327] 0 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90080687 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Once a month or more but not every week (UKB data field 20454) (Gene-based burden) 3,579 European ancestry cases, 26,396 European ancestry controls NA Illumina [124011] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90082463 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80: Endometriosis 4,475 European ancestry cases, 205,856 European ancestry controls NA Affymetrix, Illumina [330325] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90080652 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Once a week or more but not every day (UKB data field 20454) (Gene-based burden) 4,934 European ancestry cases, 25,041 European ancestry controls NA Illumina [124011] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90082464 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O16: Unspecified maternal hypertension 638 European ancestry cases, 211,224 European ancestry controls NA Affymetrix, Illumina [330249] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90080709 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum heart rate during fitness test (UKB data field 6033) (Gene-based burden) 80,492 European ancestry individuals NA Illumina [159833] 0 heart rate response to exercise http://www.ebi.ac.uk/efo/EFO_0009184 GCST90083405 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.2: Encounter for sterilization 2,861 European ancestry cases, 207,343 European ancestry controls NA Affymetrix, Illumina [330218] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081235 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum workload during fitness test (UKB data field 6032) (Gene-based burden) 80,511 European ancestry individuals NA Illumina [159836] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083404 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Aspirin (UKB data field 6154) (Gene-based burden) 62,503 European ancestry cases, 135,215 European ancestry controls NA Illumina [178466] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083445 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N90: Other noninflammatory disorders of vulva and perineum 3,237 European ancestry cases, 205,577 European ancestry controls NA Affymetrix, Illumina [328469] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080682 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Ibuprofen e.g. Nurofen (UKB data field 6154) (Gene-based burden) 66,782 European ancestry cases, 130,936 European ancestry controls NA Illumina [178466] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083446 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R92: Abnormal and inconclusive findings on diagnostic imaging of breast 927 European ancestry cases, 207,749 European ancestry controls NA Affymetrix, Illumina [328444] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080929 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Laxatives e.g. Dulcolax Senokot (UKB data field 6154) (Gene-based burden) 13,604 European ancestry cases, 184,114 European ancestry controls NA Illumina [178466] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083450 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81: Female genital prolapse 14,361 European ancestry cases, 194,168 European ancestry controls NA Affymetrix, Illumina [328168] 0 uterine prolapse http://www.ebi.ac.uk/efo/EFO_1001864 GCST90080658 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Omeprazole e.g. Zanprol (UKB data field 6154) (Gene-based burden) 29,733 European ancestry cases, 167,985 European ancestry controls NA Illumina [178466] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083449 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N76: Other inflammation of vagina and vulva 1,782 European ancestry cases, 206,704 European ancestry controls NA Affymetrix, Illumina [328124] 0 vaginal inflammation http://www.ebi.ac.uk/efo/EFO_0005757 GCST90080647 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Paracetamol (UKB data field 6154) (Gene-based burden) 98,449 European ancestry cases, 99,269 European ancestry controls NA Illumina [178466] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083447 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25: Leiomyoma of uterus 11,770 European ancestry cases, 196,439 European ancestry controls NA Affymetrix, Illumina [327949] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90079689 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Ranitidine e.g. Zantac (UKB data field 6154) (Gene-based burden) 9,009 European ancestry cases, 188,709 European ancestry controls NA Illumina [178466] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083448 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.3: Encounter for screening for malignant neoplasm of breast 1,996 European ancestry cases, 205,668 European ancestry controls NA Affymetrix, Illumina [327211] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081209 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Any other phobia e.g. disabling fear of heights or spiders (UKB data field 20544) (Gene-based burden) 1,902 European ancestry cases, 42,366 European ancestry controls NA Illumina [138642] 0 specific phobia http://www.ebi.ac.uk/efo/EFO_1001918 GCST90082630 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F53: Puerperal psychosis 2,567 European ancestry cases, 204,976 European ancestry controls NA Affymetrix, Illumina [327094] 0 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST90079816 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Any other type of psychosis or psychotic illness (UKB data field 20544) (Gene-based burden) 526 European ancestry cases, 43,738 European ancestry controls NA Illumina [138641] 0 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST90082629 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had hysterectomy - womb removed (UKB data field 3591) 18,107 European ancestry cases, 188,986 European ancestry controls NA Affymetrix, Illumina [327021] 0 hysterectomy http://www.ebi.ac.uk/efo/EFO_0003881 GCST90079065 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Obsessive compulsive disorder (UKB data field 20544) (Gene-based burden) 866 European ancestry cases, 43,403 European ancestry controls NA Illumina [138656] 0 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST90082632 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.0: Encounter for general counseling and advice on contraception 4,439 European ancestry cases, 202,477 European ancestry controls NA Affymetrix, Illumina [326394] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081233 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Panic attacks (UKB data field 20544) (Gene-based burden) 7,804 European ancestry cases, 36,479 European ancestry controls NA Illumina [138670] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90082631 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N93: Other abnormal uterine and vaginal bleeding 5,757 European ancestry cases, 201,193 European ancestry controls NA Affymetrix, Illumina [326282] 0 Metrorrhagia http://purl.obolibrary.org/obo/HP_0100608 GCST90080691 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Social anxiety or social phobia (UKB data field 20544) (Gene-based burden) 1,734 European ancestry cases, 42,543 European ancestry controls NA Illumina [138653] 0 social anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001917 GCST90082628 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N60: Benign mammary dysplasia 3,431 European ancestry cases, 203,229 European ancestry controls NA Affymetrix, Illumina [326148] 0 breast fibrocystic disease http://www.ebi.ac.uk/efo/EFO_0003014 GCST90080638 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mania, hypomania, bipolar or manic depression (UKB data field 20544) (Gene-based burden) 733 European ancestry cases, 43,534 European ancestry controls NA Illumina [138644] 0 mood disorder http://www.ebi.ac.uk/efo/EFO_0004247 GCST90082622 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O03: Spontaneous abortion 2,640 European ancestry cases, 203,668 European ancestry controls NA Affymetrix, Illumina [325703] 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90080707 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression (UKB data field 20544) (Gene-based burden) 29,907 European ancestry cases, 14,440 European ancestry controls NA Illumina [138726] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082623 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D24: Benign neoplasm of breast 1,779 European ancestry cases, 208,433 European ancestry controls NA Affymetrix, Illumina [330140] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079684 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Merkel Cell Polyomavirus (UKB data field 23067) (Gene-based burden) 5,638 European ancestry cases, 2,903 European ancestry controls NA Illumina [70714] 0 merkel cell virus seropositivity http://www.ebi.ac.uk/efo/EFO_0010906 GCST90082881 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95.1: Menopausal and female climacteric states 772 European ancestry cases, 209,359 European ancestry controls NA Affymetrix, Illumina [330025] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080696 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean corpuscular haemoglobin (UKB data field 30050) (Gene-based burden) 419,189 European ancestry individuals NA Illumina [185803] 0 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90082969 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97.5: Presence of (intrauterine) contraceptive device 1,276 European ancestry cases, 208,800 European ancestry controls NA Affymetrix, Illumina [330001] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081432 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean corpuscular haemoglobin concentration (UKB data field 30060) (Gene-based burden) 419,186 European ancestry individuals NA Illumina [185803] 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90082971 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z39: Encounter for maternal postpartum care and examination 1,977 European ancestry cases, 208,474 European ancestry controls NA Affymetrix, Illumina [329997] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081252 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean corpuscular volume (UKB data field 30040) (Gene-based burden) 419,192 European ancestry individuals NA Illumina [185803] 0 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90082968 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N61: Inflammatory disorders of breast 987 European ancestry cases, 208,795 European ancestry controls NA Affymetrix, Illumina [329665] 0 mastitis http://www.ebi.ac.uk/efo/EFO_1001034 GCST90080639 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean platelet thrombocyte volume (UKB data field 30100) (Gene-based burden) 419,184 European ancestry individuals NA Illumina [185803] 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90082975 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83: Noninflammatory disorders of ovary, fallopian tube and broad ligament 6,167 European ancestry cases, 203,364 European ancestry controls NA Affymetrix, Illumina [329446] 0 fallopian tube disease http://www.ebi.ac.uk/efo/EFO_0009548 GCST90080663 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean reticulocyte volume (UKB data field 30260) (Gene-based burden) 412,501 European ancestry individuals NA Illumina [185680] 0 mean reticulocyte volume http://www.ebi.ac.uk/efo/EFO_0010701 GCST90082988 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84: Polyp of female genital tract 12,343 European ancestry cases, 197,217 European ancestry controls NA Affymetrix, Illumina [329419] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90080666 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean sphered cell volume (UKB data field 30270) (Gene-based burden) 412,334 European ancestry individuals NA Illumina [185680] 0 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90082989 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O69: Labor and delivery complicated by umbilical cord complications 664 European ancestry cases, 211,335 European ancestry controls NA Affymetrix, Illumina [329345] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080732 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean time to correctly identify matches (UKB data field 20023) (Gene-based burden) 427,920 European ancestry individuals NA Illumina [185917] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082238 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N91: Absent, scanty and rare menstruation 743 European ancestry cases, 208,695 European ancestry controls NA Affymetrix, Illumina [329323] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080683 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean spherical equivalent (Gene-based burden) 106,495 European ancestry individuals NA Illumina [167325] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085483 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z33: Pregnant state 1,929 European ancestry cases, 207,444 European ancestry controls NA Affymetrix, Illumina [329152] 0 pregnancy http://www.ebi.ac.uk/efo/EFO_0002950 GCST90081242 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean spherical equivalent (first instance) (Gene-based burden) 93,186 European ancestry individuals NA Illumina [164300] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085482 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N97: Female infertility 1,483 European ancestry cases, 207,556 European ancestry controls NA Affymetrix, Illumina [328864] 0 female infertility http://www.ebi.ac.uk/efo/EFO_0008560 GCST90080700 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean spherical equivalent - started wearing glasses or contacts before 40 (Gene-based burden) 48,482 European ancestry individuals NA Illumina [143543] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085484 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.8: Encounter for other contraceptive management 842 European ancestry cases, 208,240 European ancestry controls NA Affymetrix, Illumina [328805] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081240 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood pressure medication use (UKB data field 6153) (Gene-based burden) 42,217 European ancestry cases, 33,337 European ancestry controls NA Illumina [26619] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083444 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N87: Dysplasia of cervix uteri 3,148 European ancestry cases, 205,857 European ancestry controls NA Affymetrix, Illumina [328658] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90080674 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Monocyte percentage (UKB data field 30190) (Gene-based burden) 418,454 European ancestry individuals NA Illumina [185795] 0 monocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007989 GCST90082982 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Ranitidine e.g. Zantac (UKB data field 6154) 9,009 European ancestry cases, 188,709 European ancestry controls NA Affymetrix, Illumina [314976] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079462 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mood swings (UKB data field 1920) (Gene-based burden) 195,051 European ancestry cases, 226,165 European ancestry controls NA Illumina [185773] 0 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST90081604 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 1 (UKB data field 2395) 63,607 European ancestry cases, 132,262 European ancestry controls NA Affymetrix, Illumina [313544] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90078944 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 500 Never (UKB data field 21029) (Gene-based burden) 34,465 European ancestry cases, 48,678 European ancestry controls NA Illumina [159601] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082688 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 2 (UKB data field 2395) 46,649 European ancestry cases, 149,220 European ancestry controls NA Affymetrix, Illumina [313544] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90078945 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 501 Sometimes (UKB data field 21029) (Gene-based burden) 29,974 European ancestry cases, 53,169 European ancestry controls NA Illumina [159601] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082689 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 3 (UKB data field 2395) 54,082 European ancestry cases, 141,787 European ancestry controls NA Affymetrix, Illumina [313544] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90078946 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 502 Often (UKB data field 21029) (Gene-based burden) 6,273 European ancestry cases, 76,870 European ancestry controls NA Illumina [159601] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082690 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 4 (UKB data field 2395) 37,404 European ancestry cases, 158,465 European ancestry controls NA Affymetrix, Illumina [313544] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90078947 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 503 Most of the time (UKB data field 21029) (Gene-based burden) 8,200 European ancestry cases, 74,943 European ancestry controls NA Illumina [159601] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082691 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Had major operations (UKB data field 2415) 127,607 European ancestry cases, 68,219 European ancestry controls NA Affymetrix, Illumina [313446] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90078948 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 504 Always (UKB data field 21029) (Gene-based burden) 4,231 European ancestry cases, 78,912 European ancestry controls NA Illumina [159601] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90082692 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N41.1: Chronic prostatitis 1,070 European ancestry cases, 193,535 European ancestry controls NA Affymetrix, Illumina [311413] 0 prostatitis http://www.ebi.ac.uk/efo/EFO_0003830 GCST90080618 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More irritable than usual during worst period of anxiety (UKB data field 20422) (Gene-based burden) 28,540 European ancestry cases, 11,134 European ancestry controls NA Illumina [134736] 0 irritability measurement http://www.ebi.ac.uk/efo/EFO_0009594 GCST90082426 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N41.9: Inflammatory disease of prostate, unspecified 712 European ancestry cases, 193,893 European ancestry controls NA Affymetrix, Illumina [311413] 0 inflammatory disease http://www.ebi.ac.uk/efo/EFO_0009903 GCST90080619 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mother still alive (UKB data field 1835) (Gene-based burden) 167,942 European ancestry cases, 255,745 European ancestry controls NA Illumina [185841] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90081601 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N43.3: Hydrocele, unspecified 1,572 European ancestry cases, 193,033 European ancestry controls NA Affymetrix, Illumina [311413] 0 testicular hydrocele http://www.ebi.ac.uk/efo/EFO_1001859 GCST90080623 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maternal age (UKB data field 1845) (Gene-based burden) 167,682 European ancestry individuals NA Illumina [176243] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90081602 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N45.9: Orchitis, epididymitis and epididymo-orchitis without abscess 931 European ancestry cases, 193,674 European ancestry controls NA Affymetrix, Illumina [311413] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90080625 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maternal age at death (UKB data field 3526) (Gene-based burden) 263,428 European ancestry individuals NA Illumina [181905] 0 mother's age at death http://www.ebi.ac.uk/efo/EFO_0009721 GCST90083046 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48.6: Induration penis plastica 937 European ancestry cases, 193,668 European ancestry controls NA Affymetrix, Illumina [311413] 0 Penile Fibromatosis http://www.ebi.ac.uk/efo/EFO_1000466 GCST90080629 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bleeding gums (UKB data field 6149) (Gene-based burden) 59,427 European ancestry cases, 115,782 European ancestry controls NA Illumina [176771] 0 Gingival bleeding http://purl.obolibrary.org/obo/HP_0000225 GCST90083424 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.6: Benign lipomatous neoplasm of spermatic cord 954 European ancestry cases, 193,651 European ancestry controls NA Affymetrix, Illumina [311411] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90079668 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Dentures (UKB data field 6149) (Gene-based burden) 74,437 European ancestry cases, 100,772 European ancestry controls NA Illumina [176771] 0 dentures http://www.ebi.ac.uk/efo/EFO_0010078 GCST90083427 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neck/shoulder pain for three months (UKB data field 3404) (Gene-based burden) 71,753 European ancestry cases, 31,678 European ancestry controls NA Illumina [165570] 0 Shoulder pain http://purl.obolibrary.org/obo/HP_0030834 GCST90083040 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 2 to 4 hours (UKB data field 104900) 5,667 European ancestry cases, 179,977 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077565 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nervous feelings (UKB data field 1970) (Gene-based burden) 102,281 European ancestry cases, 318,122 European ancestry controls NA Illumina [185803] 0 feeling nervous measurement http://www.ebi.ac.uk/efo/EFO_0009597 GCST90081609 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 30 to 60 minutes (UKB data field 104900) 31,516 European ancestry cases, 154,128 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077566 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neutrophill count (UKB data field 30140) (Gene-based burden) 418,449 European ancestry individuals NA Illumina [185795] 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90082979 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 4 to 6 hours (UKB data field 104900) 1,470 European ancestry cases, 184,174 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077567 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neutrophill percentage (UKB data field 30200) (Gene-based burden) 418,454 European ancestry individuals NA Illumina [185795] 0 neutrophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007990 GCST90082983 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 6+ hours (UKB data field 104900) 543 European ancestry cases, 185,101 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077568 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Abnormal smear cervix (Gene-based burden) 735 European ancestry cases, 331,019 European ancestry controls NA Illumina [184197] 0 abnormal PAP smear http://www.ebi.ac.uk/efo/EFO_0009511 GCST90081973 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had prostate specific antigen PSA test (UKB data field 2365) 62,851 European ancestry cases, 124,707 European ancestry controls NA Affymetrix, Illumina [303269] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90078937 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87619: abnormal smear cervix (Gene-based burden) 641 European ancestry cases, 328,411 European ancestry controls NA Illumina [184130] 0 abnormal PAP smear http://www.ebi.ac.uk/efo/EFO_0009511 GCST90081974 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oral contraceptive pill use (age of onset) (UKB data field 2794) 184,979 European ancestry individuals NA Affymetrix, Illumina [300247] 0 age at onset, contraception http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0009520 GCST90078960 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol dependency (Gene-based burden) 671 European ancestry cases, 331,083 European ancestry controls NA Illumina [184201] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90081814 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age voice broke - About average age (UKB data field 2385) 164,496 European ancestry cases, 18,349 European ancestry controls NA Affymetrix, Illumina [297204] 0 age at voice drop http://www.ebi.ac.uk/efo/EFO_0007888 GCST90078942 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y40: Adverse effects in the therapeutic use of systemic antibiotics (Gene-based burden) 943 European ancestry cases, 386,987 European ancestry controls NA Illumina [185344] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90085134 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F31: mania bipolar disorder manic depression 1,129 European ancestry cases, 327,922 European ancestry controls NA Affymetrix, Illumina [456274] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90077768 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y42: Adverse effects in the therapeutic use of hormones and their synthetic substitutes and antagonists, not elsewhere classified (Gene-based burden) 1,110 European ancestry cases, 386,820 European ancestry controls NA Illumina [185344] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90085135 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M86: Osteomyelitis 563 European ancestry cases, 328,488 European ancestry controls NA Affymetrix, Illumina [456274] 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90077778 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y43: Adverse effects in the therapeutic use of primarily systemic agents (Gene-based burden) 3,135 European ancestry cases, 384,795 European ancestry controls NA Illumina [185344] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90085137 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R42: vertigo 673 European ancestry cases, 328,379 European ancestry controls NA Affymetrix, Illumina [456274] 0 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90077902 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y43.3: Adverse effects in the therapeutic use of other antineoplastic drugs (Gene-based burden) 2,845 European ancestry cases, 385,085 European ancestry controls NA Illumina [185344] 0 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90085136 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45: Asthma 45,415 European ancestry cases, 283,636 European ancestry controls NA Affymetrix, Illumina [456273] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90077672 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y45: Adverse effects in the therapeutic use of analgesics, antipyretics and anti-inflammatory drugs (Gene-based burden) 1,339 European ancestry cases, 386,562 European ancestry controls NA Illumina [185343] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90085139 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S223: fracture rib 571 European ancestry cases, 328,481 European ancestry controls NA Affymetrix, Illumina [456273] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90077977 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y45.0: Adverse effects in the therapeutic use of opioids and related analgesics (Gene-based burden) 588 European ancestry cases, 387,342 European ancestry controls NA Illumina [185344] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90085138 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.3: Candidiasis of vulva and vagina 2,475 European ancestry cases, 203,953 European ancestry controls NA Affymetrix, Illumina [325691] 0 vulvovaginal candidiasis http://www.ebi.ac.uk/efo/EFO_0007543 GCST90079556 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Psychological over eating or binge eating (UKB data field 20544) (Gene-based burden) 604 European ancestry cases, 43,660 European ancestry controls NA Illumina [138642] 0 binge eating http://www.ebi.ac.uk/efo/EFO_0005924 GCST90082624 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O80: Encounter for full-term uncomplicated delivery 9,148 European ancestry cases, 196,653 European ancestry controls NA Affymetrix, Illumina [325120] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90080740 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anxiety, nerves or generalized anxiety disorder (UKB data field 20544) (Gene-based burden) 19,743 European ancestry cases, 24,570 European ancestry controls NA Illumina [138693] 0 generalized anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001892 GCST90082625 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N89: Other noninflammatory disorders of vagina 5,496 European ancestry cases, 197,997 European ancestry controls NA Affymetrix, Illumina [322291] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080679 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anorexia nervosa (UKB data field 20544) (Gene-based burden) 781 European ancestry cases, 43,483 European ancestry controls NA Illumina [138642] 0 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST90082626 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N63: Unspecified lump in breast 6,317 European ancestry cases, 195,686 European ancestry controls NA Affymetrix, Illumina [320743] 0 breast cyst http://www.ebi.ac.uk/efo/EFO_1000848 GCST90080641 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Agoraphobia (UKB data field 20544) (Gene-based burden) 557 European ancestry cases, 43,707 European ancestry controls NA Illumina [138641] 0 agoraphobia http://www.ebi.ac.uk/efo/EFO_1001872 GCST90082627 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92: Excessive, frequent and irregular menstruation 19,747 European ancestry cases, 181,191 European ancestry controls NA Affymetrix, Illumina [319049] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90080688 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - minutes per week for moderate activity (UKB data field 22038) (Gene-based burden) 349,393 European ancestry individuals NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082844 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30: Encounter for contraceptive management 14,142 European ancestry cases, 184,313 European ancestry controls NA Affymetrix, Illumina [316498] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081241 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - minutes per week for walking (UKB data field 22037) (Gene-based burden) 349,393 European ancestry individuals NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082843 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.4: Encounter for screening for malignant neoplasm of cervix 55,534 European ancestry cases, 143,116 European ancestry controls NA Affymetrix, Illumina [316469] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081210 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metformin medication use (Gene-based burden) 12,065 European ancestry cases, 308,693 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90085485 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95: Menopausal and other perimenopausal disorders 19,021 European ancestry cases, 178,957 European ancestry controls NA Affymetrix, Illumina [315818] 0 menopause http://www.ebi.ac.uk/efo/EFO_0003922 GCST90080698 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myocardial infarction (Gene-based burden) 17,896 European ancestry cases, 404,595 European ancestry controls NA Illumina [185842] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90085481 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Aspirin (UKB data field 6154) 62,503 European ancestry cases, 135,215 European ancestry controls NA Affymetrix, Illumina [314976] 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079459 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myocardial infarction (Gene-based burden) 15,475 European ancestry cases, 348,048 European ancestry controls NA Illumina [184927] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90085480 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Ibuprofen e.g. Nurofen (UKB data field 6154) 66,782 European ancestry cases, 130,936 European ancestry controls NA Affymetrix, Illumina [314976] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079460 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Microalbumin in urine (UKB data field 30500) (Gene-based burden) 133,436 European ancestry individuals NA Illumina [171833] 0 urinary microalbumin measurement http://www.ebi.ac.uk/efo/EFO_0010967 GCST90082993 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Laxatives e.g. Dulcolax Senokot (UKB data field 6154) 13,604 European ancestry cases, 184,114 European ancestry controls NA Affymetrix, Illumina [314976] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079464 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Miserableness (UKB data field 1930) (Gene-based burden) 186,446 European ancestry cases, 237,632 European ancestry controls NA Illumina [185842] 0 feeling miserable measurement http://www.ebi.ac.uk/efo/EFO_0009598 GCST90081605 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Omeprazole e.g. Zanprol (UKB data field 6154) 29,733 European ancestry cases, 167,985 European ancestry controls NA Affymetrix, Illumina [314976] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079463 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Monocyte count (UKB data field 30130) (Gene-based burden) 418,449 European ancestry individuals NA Illumina [185795] 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90082978 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Medication for pain relief constipation heartburn - Paracetamol (UKB data field 6154) 98,449 European ancestry cases, 99,269 European ancestry controls NA Affymetrix, Illumina [314976] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079461 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Light smokers - at least 100 smokes in lifetime (UKB data field 2644) (Gene-based burden) 55,456 European ancestry cases, 64,128 European ancestry controls NA Illumina [169246] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082940 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D05: Carcinoma in situ of breast 2,611 European ancestry cases, 209,012 European ancestry controls NA Affymetrix, Illumina [331802] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90079648 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Likelihood of resuming smoking - No definitely not (UKB data field 2936) (Gene-based burden) 94,791 European ancestry cases, 11,787 European ancestry controls NA Illumina [166087] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082959 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z34.9: Encounter for supervision of normal pregnancy, unspecified 810 European ancestry cases, 210,819 European ancestry controls NA Affymetrix, Illumina [331787] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081244 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Likelihood of resuming smoking - No probably not (UKB data field 2936) (Gene-based burden) 11,048 European ancestry cases, 95,530 European ancestry controls NA Illumina [166087] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082958 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N88: Other noninflammatory disorders of cervix uteri 2,098 European ancestry cases, 209,410 European ancestry controls NA Affymetrix, Illumina [331706] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080677 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Likelihood of resuming smoking probably (UKB data field 2936) (Gene-based burden) 1,432 European ancestry cases, 105,146 European ancestry controls NA Illumina [166087] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082957 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O99.8: Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium 803 European ancestry cases, 210,681 European ancestry controls NA Affymetrix, Illumina [331688] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90080742 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lipid lowering medication use (Gene-based burden) 78,394 European ancestry cases, 242,364 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90085479 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.6: Rectocele 5,126 European ancestry cases, 206,385 European ancestry controls NA Affymetrix, Illumina [331668] 0 rectocele http://www.ebi.ac.uk/efo/EFO_1001837 GCST90080657 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lipoprotein A levels (UKB data field 30790) (Gene-based burden) 329,317 European ancestry individuals NA Illumina [184158] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90083020 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O75: Other complications of labor and delivery, not elsewhere classified 848 European ancestry cases, 210,661 European ancestry controls NA Affymetrix, Illumina [331648] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90080738 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - logMAR final left (UKB data field 5208) (Gene-based burden) 109,433 European ancestry individuals NA Illumina [168037] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90083318 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z36: Encounter for antenatal screening of mother 1,858 European ancestry cases, 209,616 European ancestry controls NA Affymetrix, Illumina [331600] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081248 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - logMAR final right (UKB data field 5201) (Gene-based burden) 109,473 European ancestry individuals NA Illumina [168080] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90083317 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N72: Inflammatory disease of cervix uteri 1,272 European ancestry cases, 210,139 European ancestry controls NA Affymetrix, Illumina [331543] 0 Cervicitis http://purl.obolibrary.org/obo/HP_0030160 GCST90080643 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Loneliness (UKB data field 2020) (Gene-based burden) 79,904 European ancestry cases, 344,503 European ancestry controls NA Illumina [185849] 0 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST90082358 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z36.8: Encounter for other antenatal screening 622 European ancestry cases, 211,111 European ancestry controls NA Affymetrix, Illumina [331542] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081247 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Long standing illness disability or infirmity (UKB data field 2188) (Gene-based burden) 142,834 European ancestry cases, 278,602 European ancestry controls NA Illumina [185789] 0 chronic disease http://www.ebi.ac.uk/efo/EFO_0009714 GCST90082836 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N93.8: Other specified abnormal uterine and vaginal bleeding 1,858 European ancestry cases, 209,539 European ancestry controls NA Affymetrix, Illumina [331505] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90080690 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Long term recurrent antibiotics as child or teenager (UKB data field 21067) (Gene-based burden) 20,435 European ancestry cases, 120,320 European ancestry controls NA Illumina [171973] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082817 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.9: Malignant neoplasm of breast of unspecified site 8,909 European ancestry cases, 202,443 European ancestry controls 3,181 European ancestry cases, 120,979 European ancestry controls Affymetrix, Illumina [331478] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90079605 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of depression (UKB data field 4609) (Gene-based burden) 77,110 European ancestry individuals NA Illumina [158224] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90083198 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O02.1: Missed abortion 1,327 European ancestry cases, 210,010 European ancestry controls NA Affymetrix, Illumina [331470] 0 abortion http://www.ebi.ac.uk/efo/EFO_1001491 GCST90080703 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of mania or irritability - A week or more (UKB data field 20492) (Gene-based burden) 7,805 European ancestry cases, 25,470 European ancestry controls NA Illumina [128161] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082519 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Started wearing glasses or contacts before 40 192,090 European ancestry individuals NA Affymetrix, Illumina [309483] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081542 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Loose teeth (UKB data field 6149) (Gene-based burden) 18,873 European ancestry cases, 156,336 European ancestry controls NA Illumina [176771] 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90083425 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age of first facial hair - About average age (UKB data field 2375) 154,111 European ancestry cases, 36,815 European ancestry controls NA Affymetrix, Illumina [307133] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90078939 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mouth ulcers (UKB data field 6149) (Gene-based burden) 46,301 European ancestry cases, 128,908 European ancestry controls NA Illumina [176771] 0 Oral ulcer http://purl.obolibrary.org/obo/HP_0000155 GCST90083422 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age of first facial hair - Older than average (UKB data field 2375) 25,253 European ancestry cases, 165,673 European ancestry controls NA Affymetrix, Illumina [307133] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90078940 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Painful gums (UKB data field 6149) (Gene-based burden) 13,435 European ancestry cases, 161,774 European ancestry controls NA Illumina [176771] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90083423 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age of first facial hair - Younger than average (UKB data field 2375) 13,051 European ancestry cases, 177,875 European ancestry controls NA Affymetrix, Illumina [307133] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90078938 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Toothache (UKB data field 6149) (Gene-based burden) 19,161 European ancestry cases, 156,048 European ancestry controls NA Illumina [176771] 0 toothache http://www.ebi.ac.uk/efo/EFO_0010072 GCST90083426 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.6: Abnormal cytological findings in specimens from female genital organs 12,550 European ancestry cases, 177,618 European ancestry controls NA Affymetrix, Illumina [306392] 0 Abnormal morphology of female internal genitalia http://purl.obolibrary.org/obo/HP_0000008 GCST90080922 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple worries during worst period of anxiety (UKB data field 20540) (Gene-based burden) 31,523 European ancestry cases, 10,086 European ancestry controls NA Illumina [136642] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082617 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87: Abnormal findings in specimens from female genital organs 13,074 European ancestry cases, 176,246 European ancestry controls NA Affymetrix, Illumina [305348] 0 Abnormal morphology of female internal genitalia http://purl.obolibrary.org/obo/HP_0000008 GCST90080923 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia diagnosis - highly myopic (UKB data field 20262) (Gene-based burden) 3,753 European ancestry cases, 90,579 European ancestry controls NA Illumina [164624] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90082380 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol consumed (UKB data field 100580) 118,267 European ancestry cases, 67,377 European ancestry controls NA Affymetrix, Illumina [304393] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90077559 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia diagnosis - moderate low myopia (UKB data field 20262) (Gene-based burden) 24,937 European ancestry cases, 69,395 European ancestry controls NA Illumina [164624] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90082379 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coffee consumed (UKB data field 100240) 144,030 European ancestry cases, 41,614 European ancestry controls NA Affymetrix, Illumina [304393] 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90077557 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia diagnosis - non myopic (UKB data field 20262) (Gene-based burden) 65,642 European ancestry cases, 28,690 European ancestry controls NA Illumina [164624] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082378 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tea consumed (UKB data field 100390) 155,356 European ancestry cases, 30,288 European ancestry controls NA Affymetrix, Illumina [304393] 0 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST90077558 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spinal injury (Gene-based burden) 730 European ancestry cases, 328,322 European ancestry controls NA Illumina [184145] 0 Spinal cord injury http://www.ebi.ac.uk/efo/EFO_1001919 GCST90081735 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - None (UKB data field 104900) 132,094 European ancestry cases, 53,550 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077561 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-alcoholic fatty liver disease - Cirrhosis (Gene-based burden) 852 European ancestry cases, 376,493 European ancestry controls NA Illumina [185138] 0 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90085486 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - Under 10 minutes (UKB data field 104900) 49,933 European ancestry cases, 135,711 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077563 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-alcoholic fatty liver disease - Composite (Gene-based burden) 3,220 European ancestry cases, 376,493 European ancestry controls NA Illumina [185185] 0 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90085487 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 10 to 30 minutes (UKB data field 104900) 36,848 European ancestry cases, 148,796 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077562 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nasal polyps (Gene-based burden) 5,381 European ancestry cases, 381,522 European ancestry controls NA Illumina [185336] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90085488 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 1 to 2 hours (UKB data field 104900) 17,017 European ancestry cases, 168,627 European ancestry controls NA Affymetrix, Illumina [304393] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90077564 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80: Endometriosis 3,142 European ancestry cases, 174,752 European ancestry controls NA Affymetrix, Illumina [291341] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90077822 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bone disorder (Gene-based burden) 988 European ancestry cases, 330,766 European ancestry controls NA Illumina [184201] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90081755 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O13: gestational hypertension pre eclampsia 1,593 European ancestry cases, 176,301 European ancestry controls NA Affymetrix, Illumina [291341] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90077654 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M85: bone disorder (Gene-based burden) 841 European ancestry cases, 328,211 European ancestry controls NA Illumina [184145] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90081756 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94: gynaecological disorder (not cancer) 664 European ancestry cases, 177,230 European ancestry controls NA Affymetrix, Illumina [291341] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90077792 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Benign prostatic hypertrophy (Gene-based burden) 1,075 European ancestry cases, 330,679 European ancestry controls NA Illumina [184195] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90081902 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92: menorrhagia unknown cause 1,349 European ancestry cases, 176,545 European ancestry controls NA Affymetrix, Illumina [291341] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90077934 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N40: benign prostatic hypertrophy (Gene-based burden) 968 European ancestry cases, 150,190 European ancestry controls NA Illumina [172888] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90081903 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O04: miscarriage 1,240 European ancestry cases, 176,654 European ancestry controls NA Affymetrix, Illumina [291341] 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90077936 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Breast cysts (Gene-based burden) 1,900 European ancestry cases, 329,854 European ancestry controls NA Illumina [184201] 0 breast cyst http://www.ebi.ac.uk/efo/EFO_1000848 GCST90081788 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83: ovarian cyst or cysts 3,353 European ancestry cases, 174,541 European ancestry controls NA Affymetrix, Illumina [291341] 0 Tarlov Cysts http://www.ebi.ac.uk/efo/EFO_1001858 GCST90077794 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N60: breast cysts (Gene-based burden) 1,569 European ancestry cases, 176,325 European ancestry controls NA Illumina [177166] 0 breast cyst http://www.ebi.ac.uk/efo/EFO_1000848 GCST90081789 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25: uterine fibroids 6,313 European ancestry cases, 171,581 European ancestry controls NA Affymetrix, Illumina [291341] 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90077797 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bronchiectasis (Gene-based burden) 1,129 European ancestry cases, 330,625 European ancestry controls NA Illumina [184201] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90081663 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84: uterine polyps 1,299 European ancestry cases, 176,595 European ancestry controls NA Affymetrix, Illumina [291341] 0 uterine polyp http://www.ebi.ac.uk/efo/EFO_0009484 GCST90077799 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J47: Bronchiectasis (Gene-based burden) 1,030 European ancestry cases, 328,022 European ancestry controls NA Illumina [184145] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90081664 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N814: vaginal prolapse uterine prolapse 2,633 European ancestry cases, 175,261 European ancestry controls NA Affymetrix, Illumina [291341] 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90077801 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bronchitis (Gene-based burden) 3,807 European ancestry cases, 327,947 European ancestry controls NA Illumina [184201] 0 bronchial disease http://www.ebi.ac.uk/efo/EFO_1002018 GCST90081816 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking (UKB data field 4728) 40,481 European ancestry cases, 135,686 European ancestry controls NA Affymetrix, Illumina [291310] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079218 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J40: bronchitis (Gene-based burden) 3,397 European ancestry cases, 325,655 European ancestry controls NA Illumina [184145] 0 bronchial disease http://www.ebi.ac.uk/efo/EFO_1002018 GCST90081817 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - initial answer - Blue square (UKB data field 4292) 36,948 European ancestry cases, 139,119 European ancestry controls NA Affymetrix, Illumina [291246] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90079170 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carpal tunnel syndrome (Gene-based burden) 928 European ancestry cases, 330,826 European ancestry controls NA Illumina [184201] 0 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90081915 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - initial answer - Orange circle (UKB data field 4292) 141,954 European ancestry cases, 34,113 European ancestry controls NA Affymetrix, Illumina [291246] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90079171 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56: carpal tunnel syndrome (Gene-based burden) 830 European ancestry cases, 328,222 European ancestry controls NA Illumina [184145] 0 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90081916 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Extremely happy (UKB data field 4559) 37,735 European ancestry cases, 138,353 European ancestry controls NA Affymetrix, Illumina [291128] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90079194 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21: Gastro oesophageal reflux or gastric reflux 18,674 European ancestry cases, 310,377 European ancestry controls NA Affymetrix, Illumina [456273] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90077693 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y52: Adverse effects in the therapeutic use of agents primarily affecting the cardiovascular system (Gene-based burden) 862 European ancestry cases, 387,068 European ancestry controls NA Illumina [185344] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90085140 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I10: hypertension 100,205 European ancestry cases, 228,845 European ancestry controls NA Affymetrix, Illumina [456273] 1 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90077646 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y57: Adverse effects in the therapeutic use of other and unspecified drugs and medicaments (Gene-based burden) 523 European ancestry cases, 387,407 European ancestry controls NA Illumina [185344] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90085141 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M89: osteopenia 1,458 European ancestry cases, 327,593 European ancestry controls NA Affymetrix, Illumina [456273] 0 Osteopenia http://purl.obolibrary.org/obo/HP_0000938 GCST90077962 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y60: Injury due to unintentional cut, puncture, perforation or haemorrhage during surgical and medical care (Gene-based burden) 781 European ancestry cases, 387,149 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085143 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87619: abnormal smear cervix 641 European ancestry cases, 328,411 European ancestry controls NA Affymetrix, Illumina [455670] 0 abnormal PAP smear http://www.ebi.ac.uk/efo/EFO_0009511 GCST90077988 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y60.0: Injury due to unintentional cut, puncture, perforation or haemorrhage during surgical operation (Gene-based burden) 628 European ancestry cases, 387,302 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085142 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non cancer illness - year age first occurred (UKB data field 87) 327,660 European ancestry individuals NA Affymetrix, Illumina [454974] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90079504 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83: Surgical operation and other surgical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 22,401 European ancestry cases, 365,517 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085151 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of moderate activity (UKB data field 894) 327,407 European ancestry individuals NA Affymetrix, Illumina [454959] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079505 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.1: Surgical operation with implant of artificial internal device as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 7,633 European ancestry cases, 380,297 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085144 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inflammatory bowel disease - strict composite 5,509 European ancestry cases, 321,797 European ancestry controls NA Affymetrix, Illumina [454878] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90081489 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.2: Surgical operation with anastomosis, bypass or graft as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 2,578 European ancestry cases, 385,352 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085145 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ulcerative colitis 3,928 European ancestry cases, 321,797 European ancestry controls NA Affymetrix, Illumina [453384] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90081490 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.3: Surgical operation with formation of external stoma as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 544 European ancestry cases, 387,386 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085146 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Crohn's disease 2,106 European ancestry cases, 321,797 European ancestry controls NA Affymetrix, Illumina [451560] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90081488 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.4: Other reconstructive surgery as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 1,108 European ancestry cases, 386,822 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085147 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Paternal age at death (UKB data field 1807) 324,038 European ancestry individuals NA Affymetrix, Illumina [449848] 0 father's age at death http://www.ebi.ac.uk/efo/EFO_0009712 GCST90077614 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.6: Removal of other organ (partial) (total) as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 5,438 European ancestry cases, 382,492 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085148 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 Best measure (UKB data field 20150) 322,002 European ancestry individuals 25,470 European ancestry individuals Affymetrix, Illumina [449095] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90078316 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.8: Other surgical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 6,743 European ancestry cases, 381,187 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085149 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced vital capacity FVC Best measure (UKB data field 20151) 322,002 European ancestry individuals 25,470 European ancestry individuals Affymetrix, Illumina [449095] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90078317 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.9: Surgical procedure, unspecified as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 636 European ancestry cases, 387,270 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085150 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reproduciblity of spirometry measurement using ERS ATS criteria (UKB data field 20152) 250,677 European ancestry cases, 71,325 European ancestry controls NA Affymetrix, Illumina [449095] 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90078318 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma (Gene-based burden) 50,973 European ancestry cases, 280,781 European ancestry controls NA Illumina [184201] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081657 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Very unhappy (UKB data field 4537) 2,223 European ancestry cases, 174,667 European ancestry controls NA Affymetrix, Illumina [292175] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90079185 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45: Asthma (Gene-based burden) 45,415 European ancestry cases, 283,636 European ancestry controls NA Illumina [184145] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081658 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Extremely happy (UKB data field 4581) 17,249 European ancestry cases, 159,574 European ancestry controls NA Affymetrix, Illumina [292017] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90079205 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Atrial fibrillation (Gene-based burden) 3,921 European ancestry cases, 327,833 European ancestry controls NA Illumina [184201] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90081867 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Extremely unhappy (UKB data field 4581) 2,657 European ancestry cases, 174,166 European ancestry controls NA Affymetrix, Illumina [292017] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90079210 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I48: atrial fibrillation (Gene-based burden) 3,763 European ancestry cases, 325,289 European ancestry controls NA Illumina [184145] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90081868 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Moderately happy (UKB data field 4581) 80,442 European ancestry cases, 96,381 European ancestry controls NA Affymetrix, Illumina [292017] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90079207 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Back pain (Gene-based burden) 3,955 European ancestry cases, 327,799 European ancestry controls NA Illumina [184201] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90081909 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Moderately unhappy (UKB data field 4581) 14,573 European ancestry cases, 162,250 European ancestry controls NA Affymetrix, Illumina [292017] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90079208 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: back pain (Gene-based burden) 3,099 European ancestry cases, 325,953 European ancestry controls NA Illumina [184145] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90081910 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Very happy (UKB data field 4581) 66,645 European ancestry cases, 110,178 European ancestry controls NA Affymetrix, Illumina [292017] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90079206 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Back problem (Gene-based burden) 7,766 European ancestry cases, 323,988 European ancestry controls NA Illumina [184201] 0 Abnormality of the cervical spine http://purl.obolibrary.org/obo/HP_0003319 GCST90081757 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Very unhappy (UKB data field 4581) 5,019 European ancestry cases, 171,804 European ancestry controls NA Affymetrix, Illumina [292017] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90079209 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: back problem (Gene-based burden) 6,409 European ancestry cases, 322,643 European ancestry controls NA Illumina [184145] 0 Abnormality of the cervical spine http://purl.obolibrary.org/obo/HP_0003319 GCST90081758 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - Final attempt correct (UKB data field 4294) 169,042 European ancestry cases, 7,158 European ancestry controls NA Affymetrix, Illumina [291410] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90079175 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Benign breast lump (Gene-based burden) 1,671 European ancestry cases, 330,083 European ancestry controls NA Illumina [184201] 0 breast benign neoplasm http://purl.obolibrary.org/obo/MONDO_0000620 GCST90081975 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory result - Correct recall on first attempt (UKB data field 20018) 141,954 European ancestry cases, 34,246 European ancestry controls NA Affymetrix, Illumina [291410] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90078247 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N60: benign breast lump (Gene-based burden) 1,390 European ancestry cases, 176,504 European ancestry controls NA Illumina [177166] 0 breast benign neoplasm http://purl.obolibrary.org/obo/MONDO_0000620 GCST90081976 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory result - Correct recall on second attempt (UKB data field 20018) 29,799 European ancestry cases, 146,401 European ancestry controls NA Affymetrix, Illumina [291410] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90078248 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bladder problem (not cancer) (Gene-based burden) 2,768 European ancestry cases, 328,986 European ancestry controls NA Illumina [184201] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90081700 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory result - Instruction not recalled either skipped or incorrect (UKB data field 20018) 8,070 European ancestry cases, 168,130 European ancestry controls NA Affymetrix, Illumina [291410] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90078246 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32: bladder problem (not cancer) (Gene-based burden) 2,606 European ancestry cases, 326,446 European ancestry controls NA Illumina [184145] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90081701 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N60: benign breast lump 1,390 European ancestry cases, 176,504 European ancestry controls NA Affymetrix, Illumina [291341] 0 breast benign neoplasm http://purl.obolibrary.org/obo/MONDO_0000620 GCST90077990 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blistering desquamating skin disorder (Gene-based burden) 708 European ancestry cases, 331,046 European ancestry controls NA Illumina [184201] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90081843 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Very happy (UKB data field 4548) 62,558 European ancestry cases, 114,516 European ancestry controls NA Affymetrix, Illumina [292382] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90079189 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anaemia (Gene-based burden) 987 European ancestry cases, 330,767 European ancestry controls NA Illumina [184201] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90081837 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Very unhappy (UKB data field 4548) 4,566 European ancestry cases, 172,508 European ancestry controls NA Affymetrix, Illumina [292382] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90079192 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D64: anaemia (Gene-based burden) 900 European ancestry cases, 328,152 European ancestry controls NA Illumina [184145] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90081838 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Extremely happy (UKB data field 4526) 10,779 European ancestry cases, 166,237 European ancestry controls NA Affymetrix, Illumina [292375] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90079176 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Angina (Gene-based burden) 14,285 European ancestry cases, 317,469 European ancestry controls NA Illumina [184201] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90081641 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Moderately happy (UKB data field 4526) 92,186 European ancestry cases, 84,830 European ancestry controls NA Affymetrix, Illumina [292375] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90079178 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20: angina (Gene-based burden) 13,585 European ancestry cases, 315,467 European ancestry controls NA Illumina [184145] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90081642 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Moderately unhappy (UKB data field 4526) 6,747 European ancestry cases, 170,269 European ancestry controls NA Affymetrix, Illumina [292375] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90079179 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankylosing spondylitis (Gene-based burden) 1,239 European ancestry cases, 330,515 European ancestry controls NA Illumina [184201] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90081771 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Very happy (UKB data field 4526) 73,036 European ancestry cases, 103,980 European ancestry controls NA Affymetrix, Illumina [292375] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90079177 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M45: ankylosing spondylitis (Gene-based burden) 1,113 European ancestry cases, 327,939 European ancestry controls NA Illumina [184145] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90081772 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Very unhappy (UKB data field 4526) 1,144 European ancestry cases, 175,872 European ancestry controls NA Affymetrix, Illumina [292375] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90079180 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anxiety or panic attacks (Gene-based burden) 7,097 European ancestry cases, 324,657 European ancestry controls NA Illumina [184201] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90081749 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Extremely happy (UKB data field 4537) 11,089 European ancestry cases, 165,801 European ancestry controls NA Affymetrix, Illumina [292175] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90079181 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41: Anxiety or panic attacks (Gene-based burden) 5,864 European ancestry cases, 323,188 European ancestry controls NA Illumina [184145] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90081750 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Extremely unhappy (UKB data field 4537) 1,039 European ancestry cases, 175,851 European ancestry controls NA Affymetrix, Illumina [292175] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90079186 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Appendicitis (Gene-based burden) 4,527 European ancestry cases, 327,227 European ancestry controls NA Illumina [184201] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90081889 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - I am not employed (UKB data field 4537) 63,199 European ancestry cases, 113,691 European ancestry controls NA Affymetrix, Illumina [292175] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90079187 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K37: appendicitis (Gene-based burden) 4,175 European ancestry cases, 324,877 European ancestry controls NA Illumina [184145] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90081890 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Moderately happy (UKB data field 4537) 55,486 European ancestry cases, 121,404 European ancestry controls NA Affymetrix, Illumina [292175] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90079183 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arthritis nos (Gene-based burden) 4,982 European ancestry cases, 326,772 European ancestry controls NA Illumina [184201] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90081913 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Moderately unhappy (UKB data field 4537) 8,984 European ancestry cases, 167,906 European ancestry controls NA Affymetrix, Illumina [292175] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90079184 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13: arthritis nos (Gene-based burden) 4,546 European ancestry cases, 324,506 European ancestry controls NA Illumina [184145] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90081914 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Very happy (UKB data field 4537) 46,094 European ancestry cases, 130,796 European ancestry controls NA Affymetrix, Illumina [292175] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90079182 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - amlodipine 19,689 European ancestry cases, 301,069 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078095 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z00.0: Encounter for general adult medical examination (Gene-based burden) 561 European ancestry cases, 387,369 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085164 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - arimidex 764 European ancestry cases, 319,994 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078159 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01: Encounter for other special examination without complaint, suspected or reported diagnosis (Gene-based burden) 157,424 European ancestry cases, 220,162 European ancestry controls NA Illumina [185203] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085170 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - arthrotec 612 European ancestry cases, 320,146 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078063 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.3: Encounter for examination of blood pressure (Gene-based burden) 152,936 European ancestry cases, 228,996 European ancestry controls NA Illumina [185270] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085166 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - asacol 638 European ancestry cases, 320,120 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078031 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.8: Encounter for other specified special examinations (Gene-based burden) 5,418 European ancestry cases, 372,494 European ancestry controls NA Illumina [185192] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085169 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - aspirin 59,606 European ancestry cases, 261,152 European ancestry controls NA Affymetrix, Illumina [447992] 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078044 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.84: Encounter for antibody response examination (Gene-based burden) 1,714 European ancestry cases, 382,724 European ancestry controls NA Illumina [185287] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085167 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10: alcohol dependency (Gene-based burden) 611 European ancestry cases, 328,441 European ancestry controls NA Illumina [184145] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90081815 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age voice broke - Older than average (UKB data field 2385) 11,123 European ancestry cases, 171,722 European ancestry controls NA Affymetrix, Illumina [297204] 0 age at voice drop http://www.ebi.ac.uk/efo/EFO_0007888 GCST90078943 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy hypersensitivity anaphylaxis (Gene-based burden) 3,277 European ancestry cases, 328,477 European ancestry controls NA Illumina [184201] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081792 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age voice broke - Younger than average (UKB data field 2385) 8,108 European ancestry cases, 174,737 European ancestry controls NA Affymetrix, Illumina [297204] 0 age at voice drop http://www.ebi.ac.uk/efo/EFO_0007888 GCST90078941 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78: allergy hypersensitivity anaphylaxis (Gene-based burden) 2,818 European ancestry cases, 326,234 European ancestry controls NA Illumina [184145] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081793 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Started wearing glasses or contacts after 40 182,074 European ancestry individuals NA Affymetrix, Illumina [295330] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081541 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy or anaphylactic reaction to drug (Gene-based burden) 4,757 European ancestry cases, 326,997 European ancestry controls NA Illumina [184201] 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90081799 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Extremely happy (UKB data field 4548) 9,960 European ancestry cases, 167,114 European ancestry controls NA Affymetrix, Illumina [292382] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90079188 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T887: allergy or anaphylactic reaction to drug (Gene-based burden) 4,381 European ancestry cases, 324,671 European ancestry controls NA Illumina [184145] 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90081800 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Extremely unhappy (UKB data field 4548) 1,794 European ancestry cases, 175,280 European ancestry controls NA Affymetrix, Illumina [292382] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90079193 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy or anaphylactic reaction to food (Gene-based burden) 2,207 European ancestry cases, 329,547 European ancestry controls NA Illumina [184201] 0 food allergy http://www.ebi.ac.uk/efo/EFO_1001890 GCST90081797 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Moderately happy (UKB data field 4548) 90,073 European ancestry cases, 87,001 European ancestry controls NA Affymetrix, Illumina [292382] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90079190 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T780: allergy or anaphylactic reaction to food (Gene-based burden) 2,000 European ancestry cases, 327,052 European ancestry controls NA Illumina [184145] 0 food allergy http://www.ebi.ac.uk/efo/EFO_1001890 GCST90081798 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Moderately unhappy (UKB data field 4548) 17,175 European ancestry cases, 159,899 European ancestry controls NA Affymetrix, Illumina [292382] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90079191 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy to house dust mite (Gene-based burden) 533 European ancestry cases, 331,221 European ancestry controls NA Illumina [184201] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081977 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84: Other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 3,036 European ancestry cases, 384,894 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085155 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Airways medication use 36,115 European ancestry cases, 284,643 European ancestry controls NA Affymetrix, Illumina [447992] 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081450 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84.2: Radiological procedure and radiotherapy as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 654 European ancestry cases, 387,276 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085152 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anticoagulant medicine use 9,858 European ancestry cases, 310,900 European ancestry controls NA Affymetrix, Illumina [447992] 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081455 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84.6: Urinary catheterization as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 534 European ancestry cases, 387,396 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085153 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood pressure medication use 99,813 European ancestry cases, 220,945 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081464 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84.8: Other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure (Gene-based burden) 1,150 European ancestry cases, 386,780 European ancestry controls NA Illumina [185344] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90085154 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lipid lowering medication use 78,394 European ancestry cases, 242,364 European ancestry controls NA Affymetrix, Illumina [447992] 3 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081493 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y86: Sequelae of other accidents (Gene-based burden) 1,101 European ancestry cases, 386,829 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085156 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metformin medication use 12,065 European ancestry cases, 308,693 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081499 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92: Place of occurrence of the external cause (Gene-based burden) 942 European ancestry cases, 385,084 European ancestry controls NA Illumina [185305] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085160 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oral diabetes medication use 13,132 European ancestry cases, 307,626 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081503 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92.4: Street, highway and other paved roadways as the place of occurrence of the external cause (Gene-based burden) 908 European ancestry cases, 385,483 European ancestry controls NA Illumina [185307] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085159 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - adalat 1,019 European ancestry cases, 319,739 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078003 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92.41: Street and highway as the place of occurrence of the external cause (Gene-based burden) 908 European ancestry cases, 385,483 European ancestry controls NA Illumina [185307] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085158 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - adcal 1,512 European ancestry cases, 319,246 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078204 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92.410.: Unspecified street and highway as the place of occurrence of the external cause (Gene-based burden) 908 European ancestry cases, 385,483 European ancestry controls NA Illumina [185307] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085157 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - adcal 3,444 European ancestry cases, 317,314 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078193 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y93: Activity codes (Gene-based burden) 22,575 European ancestry cases, 335,156 European ancestry controls NA Illumina [184819] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085162 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - alendronate sodium 5,527 European ancestry cases, 315,231 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078156 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y93.9: Activity, unspecified (Gene-based burden) 22,561 European ancestry cases, 335,235 European ancestry controls NA Illumina [184820] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085161 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - allopurinol 5,255 European ancestry cases, 315,503 European ancestry controls NA Affymetrix, Illumina [447992] 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078077 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y95: Nosocomial condition (Gene-based burden) 2,043 European ancestry cases, 385,876 European ancestry controls NA Illumina [185344] 0 nosocomial infection http://purl.obolibrary.org/obo/MONDO_0043544 GCST90085163 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - amitriptyline 8,712 European ancestry cases, 312,046 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078089 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z00: Encounter for general examination without complaint, suspected or reported diagnosis (Gene-based burden) 929 European ancestry cases, 387,001 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085165 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.1: Encounter for screening for malignant neoplasm of intestinal tract (Gene-based burden) 8,319 European ancestry cases, 379,548 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085193 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - clonidine 589 European ancestry cases, 320,169 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078107 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.3: Encounter for screening for malignant neoplasm of breast (Gene-based burden) 1,996 European ancestry cases, 205,668 European ancestry controls NA Illumina [179639] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085195 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - clopidogrel 3,279 European ancestry cases, 317,479 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078197 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.39: Encounter for other screening for malignant neoplasm of breast (Gene-based burden) 1,943 European ancestry cases, 381,627 European ancestry controls NA Illumina [185238] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085194 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - co-codamol 10,402 European ancestry cases, 310,356 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078161 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.4: Encounter for screening for malignant neoplasm of cervix (Gene-based burden) 55,534 European ancestry cases, 143,116 European ancestry controls NA Illumina [178971] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085196 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - co-dydramol 2,752 European ancestry cases, 318,006 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078162 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13: Encounter for screening for other diseases and disorders (Gene-based burden) 40,310 European ancestry cases, 291,703 European ancestry controls NA Illumina [184312] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085206 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - coenzyme q10/ubiquinone bio-quinone/coenzyme q10 1,629 European ancestry cases, 319,129 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078234 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.0: Encounter for screening for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (Gene-based burden) 3,572 European ancestry cases, 383,893 European ancestry controls NA Illumina [185332] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085198 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - cod liver oil 25,871 European ancestry cases, 294,887 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078134 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.1: Encounter for screening for diabetes mellitus (Gene-based burden) 1,161 European ancestry cases, 384,967 European ancestry controls NA Illumina [185301] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085200 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - codeine 2,430 European ancestry cases, 318,328 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078115 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.10: Encounter for screening for diabetes mellitus (Gene-based burden) 902 European ancestry cases, 385,224 European ancestry controls NA Illumina [185301] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085199 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - colofac 554 European ancestry cases, 320,204 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078195 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.6: Encounter for screening for cardiovascular disorders (Gene-based burden) 5,026 European ancestry cases, 374,645 European ancestry controls NA Illumina [185244] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085201 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dermovate cream 697 European ancestry cases, 320,061 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078104 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.8: Encounter for screening for other specified diseases and disorders (Gene-based burden) 8,520 European ancestry cases, 366,567 European ancestry controls NA Illumina [185174] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085204 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - desloratadine 579 European ancestry cases, 320,179 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078205 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.83: Encounter for screening for respiratory disorder NEC (Gene-based burden) 3,410 European ancestry cases, 377,130 European ancestry controls NA Illumina [185245] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085202 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - detrusitol 685 European ancestry cases, 320,073 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078191 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.89: Encounter for screening for other disorder (Gene-based burden) 1,891 European ancestry cases, 380,370 European ancestry controls NA Illumina [185267] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085203 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diazepam 1,211 European ancestry cases, 319,547 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078022 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L13: blistering desquamating skin disorder (Gene-based burden) 653 European ancestry cases, 328,399 European ancestry controls NA Illumina [184145] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90081844 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N60: breast cysts 1,569 European ancestry cases, 176,325 European ancestry controls NA Affymetrix, Illumina [291341] 0 breast cyst http://www.ebi.ac.uk/efo/EFO_1000848 GCST90077803 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - aspirin 2,789 European ancestry cases, 317,969 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078006 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.89: Encounter for other specified special examinations (Gene-based burden) 2,191 European ancestry cases, 379,100 European ancestry controls NA Illumina [185249] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085168 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - atenolol 16,805 European ancestry cases, 303,953 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078039 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z02: Encounter for administrative examination (Gene-based burden) 5,475 European ancestry cases, 378,305 European ancestry controls NA Illumina [185301] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085173 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - atorvastatin 16,654 European ancestry cases, 304,104 European ancestry controls NA Affymetrix, Illumina [447992] 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078178 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z02.8: Encounter for other administrative examinations (Gene-based burden) 3,011 European ancestry cases, 384,651 European ancestry controls NA Illumina [185333] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085171 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - azathioprine 928 European ancestry cases, 319,830 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078052 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z02.9: Encounter for administrative examinations, unspecified (Gene-based burden) 2,204 European ancestry cases, 383,513 European ancestry controls NA Illumina [185327] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085172 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beclazone inhaler 1,240 European ancestry cases, 319,518 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078016 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03: Encounter for medical observation for suspected diseases and conditions ruled out (Gene-based burden) 12,954 European ancestry cases, 374,871 European ancestry controls NA Illumina [185342] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085179 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beclometasone 4,114 European ancestry cases, 316,644 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078138 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.1: Observation for suspected malignant neoplasm (Gene-based burden) 868 European ancestry cases, 387,062 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085174 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beclomethasone 1,802 European ancestry cases, 318,956 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078120 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.4: Observation for suspected myocardial infarction (Gene-based burden) 2,726 European ancestry cases, 385,204 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085175 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beconase nasal spray 3,080 European ancestry cases, 317,678 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078080 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.5: Observation for other suspected cardiovascular diseases (Gene-based burden) 1,523 European ancestry cases, 386,346 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085176 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - becotide inhaler 2,769 European ancestry cases, 317,989 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078015 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.8: Encounter for observation for other suspected diseases and conditions ruled out (Gene-based burden) 7,113 European ancestry cases, 380,817 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085177 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bendrofluazide 2,528 European ancestry cases, 318,230 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078037 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.9: Observation for suspected disease or condition, unspecified (Gene-based burden) 658 European ancestry cases, 387,272 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085178 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bendroflumethiazide 24,581 European ancestry cases, 296,177 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078230 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z04: Encounter for examination and observation for other reasons (Gene-based burden) 2,344 European ancestry cases, 385,137 European ancestry controls NA Illumina [185338] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085182 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - betahistine 1,383 European ancestry cases, 319,375 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078133 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z04.3: Encounter for examination and observation following other accident (Gene-based burden) 524 European ancestry cases, 387,401 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085180 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - betnovate cream 1,563 European ancestry cases, 319,195 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078103 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z04.8: Encounter for examination and observation for other specified reasons (Gene-based burden) 923 European ancestry cases, 387,005 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085181 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bisoprolol 7,618 European ancestry cases, 313,140 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078091 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08: Encounter for follow-up examination after completed treatment for malignant neoplasm (Gene-based burden) 6,079 European ancestry cases, 381,838 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085186 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bricanyl inhaler 1,019 European ancestry cases, 319,739 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078014 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08.0: Follow-up examination after surgery for malignant neoplasm (Gene-based burden) 4,711 European ancestry cases, 383,219 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085183 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - budesonide 961 European ancestry cases, 319,797 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078017 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08.7: Follow-up examination after combined treatment for malignant neoplasm (Gene-based burden) 1,255 European ancestry cases, 386,675 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085184 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcichew 1,095 European ancestry cases, 319,663 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078058 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08.9: Follow-up examination after unspecified treatment for malignant neoplasm (Gene-based burden) 985 European ancestry cases, 386,945 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085185 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcichew 4,553 European ancestry cases, 316,205 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078061 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09: Encounter for follow-up examination after completed treatment for conditions other than malignant neoplasm (Gene-based burden) 18,227 European ancestry cases, 364,940 European ancestry controls NA Illumina [185289] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085191 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcium carbonate cholecalciferol 750 European ancestry cases, 320,008 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078180 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.0: Follow-up examination after surgery for other conditions (Gene-based burden) 5,895 European ancestry cases, 382,035 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085187 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcium salts 2,735 European ancestry cases, 318,023 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078057 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.2: Follow-up examination after chemotherapy for other conditions (Gene-based burden) 1,891 European ancestry cases, 386,039 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085188 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcium vitamin d 2,081 European ancestry cases, 318,677 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90077995 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.8: Follow-up examination after other treatment for other conditions (Gene-based burden) 3,238 European ancestry cases, 384,692 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085189 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - candesartan cilexetil 5,111 European ancestry cases, 315,647 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078187 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.9: Follow-up examination after unspecified treatment for other conditions (Gene-based burden) 3,011 European ancestry cases, 384,919 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085190 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - cetirizine 5,250 European ancestry cases, 315,508 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078108 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z11: Encounter for screening for infectious and parasitic diseases (Gene-based burden) 923 European ancestry cases, 385,624 European ancestry controls NA Illumina [185330] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085192 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - chondroitin product 5,753 European ancestry cases, 315,005 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078233 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12: Encounter for screening for malignant neoplasms (Gene-based burden) 63,956 European ancestry cases, 309,749 European ancestry controls NA Illumina [185144] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085197 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - citalopram 7,990 European ancestry cases, 312,768 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078153 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-11-12 34104963 Thompson A 2021-06-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34104963 Assessing the impact of alcohol consumption on the genetic contribution to mean corpuscular volume. Mean corpuscular volume 362,595 British ancestry individuals NA Affymetrix [NR] (imputed) 212 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90056174 Genome-wide genotyping array 2022-07-29 35758599 Lin CY 2022-06-27 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/35758599 Genetic contributions to female gout and hyperuricemia using genome-wide association study and polygenic risk score analyses. Gout (age >=50) 236 East Asian ancestry cases, 19,345 East Asian ancestry controls NA Affymetrix [410037] 4 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90129645 Genome-wide genotyping array 2022-07-29 35758599 Lin CY 2022-06-27 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/35758599 Genetic contributions to female gout and hyperuricemia using genome-wide association study and polygenic risk score analyses. Gout (age <50) 72 East Asian ancestry cases, 17,965 East Asian ancestry controls NA Affymetrix [410037] 1 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90129646 Genome-wide genotyping array 2022-07-29 35758599 Lin CY 2022-06-27 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/35758599 Genetic contributions to female gout and hyperuricemia using genome-wide association study and polygenic risk score analyses. Asymptomatic hyperuricaemia (age >=50) 5,190 East Asian ancestry cases, 19,345 East Asian ancestry controls NA Affymetrix [410037] 8 hyperuricemia http://www.ebi.ac.uk/efo/EFO_0009104 GCST90129647 Genome-wide genotyping array 2022-07-29 35758599 Lin CY 2022-06-27 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/35758599 Genetic contributions to female gout and hyperuricemia using genome-wide association study and polygenic risk score analyses. Asymptomatic hyperuricaemia (age <50) 2,115 East Asian ancestry cases, 17,965 East Asian ancestry controls NA Affymetrix [410037] 5 hyperuricemia http://www.ebi.ac.uk/efo/EFO_0009104 GCST90129648 Genome-wide genotyping array 2021-10-18 34265237 Roychowdhury T 2021-07-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34265237 Regulatory variants in TCF7L2 are associated with thoracic aortic aneurysm. Thoracic aortic aneurysms 1,351 European ancestry cases, 18,295 European ancestry controls 7,919 white British ancestry cases, 403,354 white British ancestry controls Illumina [22980809] (imputed) 3 thoracic aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0004282 GCST90027266 Genome-wide genotyping array 2021-08-23 34378841 Garcia-Etxebarria K 2021-08-11 Neurogastroenterol Motil www.ncbi.nlm.nih.gov/pubmed/34378841 A survey of functional dyspepsia in 361,360 individuals: Phenotypic and genetic cross-disease analyses. Functional dyspepsia 10,078 European ancestry cases, 351,282 European ancestry controls 192 cases, 442 controls Affymetrix, Illumina [7347476] (imputed) 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90010719 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiales_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027672 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027673 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027674 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Oscillospiraceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027675 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027676 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia.o_Erysipelotrichales.f_Erysipelotrichaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027677 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Acidaminococcaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027678 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Veillonellaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027679 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Burkholderiales_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027680 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Oxalobacteraceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027681 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Sutterellaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027682 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria.o_Desulfovibrionales.f_Desulfovibrionaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027683 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Enterobacteriales.f_Enterobacteriaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027684 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Pasteurellales.f_Pasteurellaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027685 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Verrucomicrobia.c_Verrucomicrobiae.o_Verrucomicrobiales.f_Verrucomicrobiaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027686 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Actinomycetales.f_Micrococcaceae.g_Rothia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027687 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Bifidobacteriales.f_Bifidobacteriaceae.g_Bifidobacterium) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027688 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ANAEROFRUCAT.PWY..homolactic.fermentation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027446 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ANAGLYCOLYSIS.PWY..glycolysis.III..from.glucose.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027447 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ARGDEG.PWY..superpathway.of.L.arginine..putrescine..and.4.aminobutanoate.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027448 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ARGORNPROST.PWY..arginine..ornithine.and.proline.interconversion) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027449 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ARO.PWY..chorismate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027450 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ASPASN.PWY..superpathway.of.L.aspartate.and.L.asparagine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027451 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (AST.PWY..L.arginine.degradation.II..AST.pathway.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027452 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (BRANCHED.CHAIN.AA.SYN.PWY..superpathway.of.branched.amino.acid.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027453 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (TRPSYN.PWY..L.tryptophan.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027647 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (UBISYN.PWY..superpathway.of.ubiquinol.8.biosynthesis..prokaryotic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027648 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (UDPNAGSYN.PWY..UDP.N.acetyl.D.glucosamine.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027649 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (X1CMET2.PWY..N10.formyl.tetrahydrofolate.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027650 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027651 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027652 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027653 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027654 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027655 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027656 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027657 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027658 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027659 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Verrucomicrobia.c_Verrucomicrobiae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027660 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Actinomycetales.f_Micrococcaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027661 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Bifidobacteriales.f_Bifidobacteriaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027662 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027663 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027664 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidales_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027665 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027666 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Prevotellaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027667 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027668 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Lactobacillaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027669 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Streptococcaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027670 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiaceae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027671 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (HEMESYN2.PWY..heme.biosynthesis.II..anaerobic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027479 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (HEXITOLDEGSUPER.PWY..superpathway.of.hexitol.degradation..bacteria.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027480 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (HISDEG.PWY..L.histidine.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027481 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (HISTSYN.PWY..L.histidine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027482 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (HOMOSER.METSYN.PWY..L.methionine.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027483 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (HSERMETANA.PWY..L.methionine.biosynthesis.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027484 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ILEUSYN.PWY..L.isoleucine.biosynthesis.I..from.threonine.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027485 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (KDO.NAGLIPASYN.PWY..superpathway.of..Kdo.2.lipid.A.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027486 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (KETOGLUCONMET.PWY..ketogluconate.metabolism) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027487 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (LACTOSECAT.PWY..lactose.and.galactose.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027488 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (METHGLYUT.PWY..superpathway.of.methylglyoxal.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027489 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (NAGLIPASYN.PWY..lipid.IVA.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027490 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (NONMEVIPP.PWY..methylerythritol.phosphate.pathway.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027491 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (NONOXIPENT.PWY..pentose.phosphate.pathway..non.oxidative.branch.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027492 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ORNDEG.PWY..superpathway.of.ornithine.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027493 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P105.PWY..TCA.cycle.IV..2.oxoglutarate.decarboxylase.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027494 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P108.PWY..pyruvate.fermentation.to.propanoate.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027495 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P122.PWY..heterolactic.fermentation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027496 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P161.PWY..acetylene.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027497 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P162.PWY..L.glutamate.degradation.V..via.hydroxyglutarate.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027498 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P164.PWY..purine.nucleobases.degradation.I..anaerobic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027499 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P23.PWY..reductive.TCA.cycle.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027500 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P42.PWY..incomplete.reductive.TCA.cycle) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027501 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P441.PWY..superpathway.of.N.acetylneuraminate.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027502 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (P461.PWY..hexitol.fermentation.to.lactate..formate..ethanol.and.acetate) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027503 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6151..S.adenosyl.L.methionine.cycle.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027572 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6163..chorismate.biosynthesis.from.3.dehydroquinate) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027573 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.621..sucrose.degradation.III..sucrose.invertase.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027574 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6263..superpathway.of.menaquinol.8.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027575 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6284..superpathway.of.unsaturated.fatty.acids.biosynthesis..E..coli.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027576 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6285..superpathway.of.fatty.acids.biosynthesis..E..coli.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027577 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6317..galactose.degradation.I..Leloir.pathway.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027578 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6353..purine.nucleotides.degradation.II..aerobic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027579 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6471..peptidoglycan.biosynthesis.IV..Enterococcus.faecium.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027580 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6507..4.deoxy.L.threo.hex.4.enopyranuronate.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027581 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6519..8.amino.7.oxononanoate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027582 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6545..pyrimidine.deoxyribonucleotides.de.novo.biosynthesis.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027583 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6588..pyruvate.fermentation.to.acetone) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027584 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6590..superpathway.of.Clostridium.acetobutylicum.acidogenic.fermentation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027585 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6608..guanosine.nucleotides.degradation.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027586 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6609..adenine.and.adenosine.salvage.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027587 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6612..superpathway.of.tetrahydrofolate.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027588 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6628..superpathway.of.L.phenylalanine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027589 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6629..superpathway.of.L.tryptophan.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027590 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6630..superpathway.of.L.tyrosine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027591 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY66.422..D.galactose.degradation.V..Leloir.pathway.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027592 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6690..cinnamate.and.3.hydroxycinnamate.degradation.to.2.oxopent.4.enoate) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027593 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6700..queuosine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027594 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6703..preQ0.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027595 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6708..ubiquinol.8.biosynthesis..prokaryotic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027596 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7328..superpathway.of.UDP.glucose.derived.O.antigen.building.blocks.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027622 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7371..1.4.dihydroxy.6.naphthoate.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027623 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7392..taxadiene.biosynthesis..engineered.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027624 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7400..L.arginine.biosynthesis.IV..archaebacteria.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027625 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7446..sulfoglycolysis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027626 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7456..mannan.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027627 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.841..superpathway.of.purine.nucleotides.de.novo.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027628 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_ARG.POLYAMINE.SYN..superpathway.of.arginine.and.polyamine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027629 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_GLYCOLYSIS.E.D..superpathway.of.glycolysis.and.Entner.Doudoroff) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027630 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_GLYCOLYSIS..glycolysis.I..from.glucose.6.phosphate.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027631 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_GLYOXYLATE.BYPASS..glyoxylate.cycle) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027632 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_HEME.BIOSYNTHESIS.II..heme.biosynthesis.I..aerobic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027633 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_NAD.BIOSYNTHESIS.II..NAD.salvage.pathway.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027634 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_REDCITCYC..TCA.cycle.VIII..helicobacter.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027635 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY_TCA.GLYOX.BYPASS..superpathway.of.glyoxylate.bypass.and.TCA) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027636 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PYRIDNUCSAL.PWY..NAD.salvage.pathway.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027637 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PYRIDNUCSYN.PWY..NAD.biosynthesis.I..from.aspartate.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027638 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PYRIDOXSYN.PWY..pyridoxal.5..phosphate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027639 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (RHAMCAT.PWY..L.rhamnose.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027640 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (RIBOSYN2.PWY..flavin.biosynthesis.I..bacteria.and.plants.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027641 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (SER.GLYSYN.PWY..superpathway.of.L.serine.and.glycine.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027642 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (SO4ASSIM.PWY..sulfate.reduction.I..assimilatory.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027643 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (SULFATE.CYS.PWY..superpathway.of.sulfate.assimilation.and.cysteine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027644 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (THRESYN.PWY..superpathway.of.L.threonine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027645 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (TRNA.CHARGING.PWY..tRNA.charging) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027646 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (COA.PWY..coenzyme.A.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027454 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (COBALSYN.PWY..adenosylcobalamin.salvage.from.cobinamide.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027455 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (COLANSYN.PWY..colanic.acid.building.blocks.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027456 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (COMPLETE.ARO.PWY..superpathway.of.aromatic.amino.acid.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027457 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (CRNFORCAT.PWY..creatinine.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027458 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (DAPLYSINESYN.PWY..L.lysine.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027459 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (DENOVOPURINE2.PWY..superpathway.of.purine.nucleotides.de.novo.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027460 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (DTDPRHAMSYN.PWY..dTDP.L.rhamnose.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027461 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ECASYN.PWY..enterobacterial.common.antigen.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027462 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (ENTBACSYN.PWY..enterobactin.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027463 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (FAO.PWY..fatty.acid..beta..oxidation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027464 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (FERMENTATION.PWY..mixed.acid.fermentation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027465 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (FUCCAT.PWY..fucose.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027466 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (FUC.RHAMCAT.PWY..superpathway.of.fucose.and.rhamnose.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027467 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GALACTARDEG.PWY..D.galactarate.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027468 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GALACT.GLUCUROCAT.PWY..superpathway.of.hexuronide.and.hexuronate.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027469 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GALACTUROCAT.PWY..D.galacturonate.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027470 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GLCMANNANAUT.PWY..superpathway.of.N.acetylglucosamine..N.acetylmannosamine.and.N.acetylneuraminate.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027471 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GLUCARDEG.PWY..D.glucarate.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027472 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GLUCONEO.PWY..gluconeogenesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027473 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GLUCOSE1PMETAB.PWY..glucose.and.glucose.1.phosphate.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027474 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GLYCOCAT.PWY..glycogen.degradation.I..bacterial.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027475 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GLYCOGENSYNTH.PWY..glycogen.biosynthesis.I..from.ADP.D.Glucose.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027476 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GLYCOL.GLYOXDEG.PWY..superpathway.of.glycol.metabolism.and.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027477 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (GOLPDLCAT.PWY..superpathway.of.glycerol.degradation.to.1.3.propanediol) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027478 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6731..starch.degradation.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027597 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6737..starch.degradation.V) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027598 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6823..molybdenum.cofactor.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027599 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6891..thiazole.biosynthesis.II..Bacillus.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027600 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6892..thiazole.biosynthesis.I..E..coli.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027601 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6897..thiamin.salvage.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027602 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6901..superpathway.of.glucose.and.xylose.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027603 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6969..TCA.cycle.V..2.oxoglutarate.ferredoxin.oxidoreductase.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027604 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7003..glycerol.degradation.to.butanol) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027605 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7013..L.1.2.propanediol.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027606 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7187..pyrimidine.deoxyribonucleotides.de.novo.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027607 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7196..superpathway.of.pyrimidine.ribonucleosides.salvage) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027608 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7197..pyrimidine.deoxyribonucleotide.phosphorylation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027609 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7198..pyrimidine.deoxyribonucleotides.de.novo.biosynthesis.IV) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027610 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7199..pyrimidine.deoxyribonucleosides.salvage) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027611 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7209..superpathway.of.pyrimidine.ribonucleosides.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027612 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7211..superpathway.of.pyrimidine.deoxyribonucleotides.de.novo.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027613 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7219..adenosine.ribonucleotides.de.novo.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027614 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7221..guanosine.ribonucleotides.de.novo.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027615 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7234..inosine.5..phosphate.biosynthesis.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027616 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7237..myo...chiro..and.scillo.inositol.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027617 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.724..superpathway.of.L.lysine..L.threonine.and.L.methionine.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027618 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7254..TCA.cycle.VII..acetate.producers.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027619 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7315..dTDP.N.acetylthomosamine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027620 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.7323..superpathway.of.GDP.mannose.derived.O.antigen.building.blocks.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027621 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PANTO.PWY..phosphopantothenate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027504 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PANTOSYN.PWY..pantothenate.and.coenzyme.A.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027505 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PENTOSE.P.PWY..pentose.phosphate.pathway) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027506 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PEPTIDOGLYCANSYN.PWY..peptidoglycan.biosynthesis.I..meso.diaminopimelate.containing.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027507 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PHOSLIPSYN.PWY..superpathway.of.phospholipid.biosynthesis.I..bacteria.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027508 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (POLYAMINSYN3.PWY..superpathway.of.polyamine.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027509 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (POLYAMSYN.PWY..superpathway.of.polyamine.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027510 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (POLYISOPRENSYN.PWY..polyisoprenoid.biosynthesis..E..coli.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027511 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PPGPPMET.PWY..ppGpp.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027512 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PRPP.PWY..superpathway.of.histidine..purine..and.pyrimidine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027513 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1061..superpathway.of.L.alanine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027514 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1241..ADP.L.glycero..beta..D.manno.heptose.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027515 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1261..anhydromuropeptides.recycling) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027516 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1296..purine.ribonucleosides.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027517 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1297..superpathway.of.purine.deoxyribonucleosides.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027518 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1298..superpathway.of.pyrimidine.deoxyribonucleosides.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027519 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1338..polymyxin.resistance) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027520 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1415..superpathway.of.heme.biosynthesis.from.uroporphyrinogen.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027521 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1479..tRNA.processing) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027522 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1533..methylphosphonate.degradation.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027523 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.1586..peptidoglycan.maturation..meso.diaminopimelate.containing.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027524 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.162..superpathway.of.pyrimidine.ribonucleotides.de.novo.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027525 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.781..aspartate.superpathway) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027526 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY0.845..superpathway.of.pyridoxal.5..phosphate.biosynthesis.and.salvage) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027527 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.1269..CMP.3.deoxy.D.manno.octulosonate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027528 Genome-wide genotyping array 2021-09-24 34506852 Chang X 2021-09-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34506852 A genome-wide association meta-analysis identifies new Eosinophilic esophagitis loci. Eosinophilic esophagitis 1,288 European ancestry male cases, 6,548 European ancestry male controls NA Illumina [11310926] (imputed) 7 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST012381 Genome-wide genotyping array 2021-09-24 34506852 Chang X 2021-09-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34506852 A genome-wide association meta-analysis identifies new Eosinophilic esophagitis loci. Eosinophilic esophagitis 1,930 European ancestry cases, 13,634 European ancestry controls NA Illumina [11310926] (imputed) 15 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST90027899 Genome-wide genotyping array 2021-09-24 34506852 Chang X 2021-09-07 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34506852 A genome-wide association meta-analysis identifies new Eosinophilic esophagitis loci. Eosinophilic esophagitis 542 European ancestry cases, 7,146 European ancestry controls NA Illumina [11310926] (imputed) 4 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST012380 Genome-wide genotyping array 2021-09-09 34185429 Tian J 2021-06-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/34185429 Aberrant MCM10 SUMOylation induces genomic instability mediated by a genetic variant associated with survival of esophageal squamous cell carcinoma. Survival time in esophageal squamous cell carcinoma 904 Han Chinese ancestry cases 503 Han Chinese ancestry cases Illumina [Exome array] 1 survival time http://www.ebi.ac.uk/efo/EFO_0000714 GCST012356 Exome genotyping array [Exome array] 2022-03-22 35232999 Garcia-Etxebarria K 2022-03-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35232999 Local genetic variation of inflammatory bowel disease in Basque population and its effect in risk prediction. Inflammatory bowel disease 498 European ancestry cases, 935 European ancestry controls NA Illumina [5411567] (imputed) 14 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90020070 Genome-wide genotyping array 2022-03-22 35232999 Garcia-Etxebarria K 2022-03-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35232999 Local genetic variation of inflammatory bowel disease in Basque population and its effect in risk prediction. Crohn's disease 284 European ancestry cases, 935 European ancestry controls NA Illumina [5411261] (imputed) 15 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90020071 Genome-wide genotyping array 2022-03-22 35232999 Garcia-Etxebarria K 2022-03-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35232999 Local genetic variation of inflammatory bowel disease in Basque population and its effect in risk prediction. Ulcerative colitis 208 European ancestry cases, 935 European ancestry controls NA Illumina [5409651] (imputed) 11 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90020072 Genome-wide genotyping array 2021-10-01 34260947 Lores-Motta L 2021-07-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260947 Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. Complement factor H levels 416 European ancestry individuals NA Illumina [9351109] (imputed) 1 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90019041 Genome-wide genotyping array 2021-10-01 34260947 Lores-Motta L 2021-07-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260947 Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. Complement factor H-related protein 1 levels 402 European ancestry individuals NA Illumina [9351109] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019042 Genome-wide genotyping array 2021-10-01 34260947 Lores-Motta L 2021-07-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260947 Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. Complement factor H-related protein 2 levels 416 European ancestry individuals NA Illumina [9340382] (imputed) 4 complement factor H-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0600055 GCST90019043 Genome-wide genotyping array 2021-10-01 34260947 Lores-Motta L 2021-07-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260947 Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. Complement factor H-related protein 3 levels 416 European ancestry individuals NA Illumina [9351109] (imputed) 2 complement factor H-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0600056 GCST90019044 Genome-wide genotyping array 2021-10-01 34260947 Lores-Motta L 2021-07-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260947 Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. Complement factor H-related protein 4A levels 416 European ancestry individuals NA Illumina [9351109] (imputed) 3 complement factor H-related protein 4A measurement http://www.ebi.ac.uk/efo/EFO_0600057 GCST90019045 Genome-wide genotyping array 2021-10-01 34260947 Lores-Motta L 2021-07-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260947 Common haplotypes at the CFH locus and low-frequency variants in CFHR2 and CFHR5 associate with systemic FHR concentrations and age-related macular degeneration. Complement factor H-related protein 5 levels 416 European ancestry individuals NA Illumina [9351109] (imputed) 1 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90019046 Genome-wide genotyping array 2021-10-26 34404248 Tsao YC 2021-08-18 Cephalalgia www.ncbi.nlm.nih.gov/pubmed/34404248 Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population. Headache 2,084 Taiwanese ancestry cases, 11,822 Taiwanese ancestry controls NA Affymetrix [7842171] (imputed) 13 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90029067 Genome-wide genotyping array 2023-02-24 34392144 Hikino K 2021-08-12 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34392144 Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias. Inguinal hernia 1,983 Japanese ancestry cases, 172,507 Japanese ancestry controls 15,995 British ancestry cases, 361,617 British ancestry controls Illumina [8443696] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90027861 Genome-wide genotyping array 2023-02-24 34392144 Hikino K 2021-08-12 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34392144 Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias. Inguinal hernia 1,626 Japanese ancestry male cases, 90,372 Japanese ancestry male controls NA Illumina [8443696] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90250830 Genome-wide genotyping array 2023-02-24 34392144 Hikino K 2021-08-12 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34392144 Susceptibility loci and polygenic architecture highlight population specific and common genetic features in inguinal hernias: genetics in inguinal hernias. Inguinal hernia 357 Japanese ancestry female cases, 82,135 Japanese ancestry female controls NA Illumina [8443696] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90250831 Genome-wide genotyping array 2021-11-02 34493870 Wightman DP 2021-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34493870 A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. Late-onset Alzheimer's disease 43,725 European ancestry cases, 46,613 European ancestry proxy cases, 1,036,225 European ancestry controls NA Illumina [NR] (imputed) 38 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST90044699 Genome-wide genotyping array 2023-10-09 34493870 Wightman DP 2021-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34493870 A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. Late-onset Alzheimer's disease 39,918 European ancestry cases, 46,613 European ancestry proxy cases, 676,386 European ancestry controls NA Illumina [12688340] (imputed) 0 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST013197 Genome-wide genotyping array 2023-10-09 34493870 Wightman DP 2021-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34493870 A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer's disease. Late-onset Alzheimer's disease 39,918 European ancestry cases, 358,140 European ancestry controls NA Illumina [12206525] (imputed) 0 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST013196 Genome-wide genotyping array 2021-11-01 34668383 Leskela J 2021-10-20 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/34668383 Genetic Profile of Endotoxemia Reveals an Association With Thromboembolism and Stroke. Serum lipopolysaccharide activity 11,296 European ancestry individuals NA Affymetrix, Illumina [9900000] (imputed) 5 serum lipopolysaccharide activity http://www.ebi.ac.uk/efo/EFO_0600064 GCST90032674 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Gastric or stomach ulcers 3,531 cases, 481,067 controls NA NR [9886868] 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90038625 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Muscle or soft tissue injuries 3,470 cases, 481,128 controls NA NR [9886868] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90038667 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Muscle or soft tissue problem 10,007 cases, 474,591 controls NA NR [9886868] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90038655 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Musculoskeletal disorder or trauma 106,605 cases, 377,993 controls NA NR [9886868] 0 musculoskeletal system disease, injury http://www.ebi.ac.uk/efo/EFO_0009676, http://www.ebi.ac.uk/efo/EFO_0000546 GCST90038601 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Myocardial infarction 11,081 cases, 473,517 controls NA NR [9886868] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90038610 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Glaucoma 5,126 cases, 479,472 controls NA NR [9886868] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90038648 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Gout 6,810 cases, 477,788 controls NA NR [9886868] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90038687 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Allergic rhinitis 27,415 cases, 457,183 controls NA NR [9886868] 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90038664 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Nervous system infection 2,361 cases, 482,237 controls NA NR [9886868] 0 infectious disorder of the nervous system http://purl.obolibrary.org/obo/MONDO_0020010 GCST90038642 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Neurological disease 32,651 cases, 451,947 controls NA NR [9886868] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90038638 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Neurological injury 2,646 cases, 481,952 controls NA NR [9886868] 0 nervous system injury http://www.ebi.ac.uk/efo/EFO_0009490 GCST90038639 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Neurological, eye or psychiatric disease 83,484 cases, 401,114 controls NA NR [9886868] 0 nervous system disease, psychiatric disorder, eye disease http://www.ebi.ac.uk/efo/EFO_0000618, http://purl.obolibrary.org/obo/MONDO_0002025, http://www.ebi.ac.uk/efo/EFO_0003966 GCST90038600 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Osteoarthritis 39,515 cases, 445,083 controls NA NR [9886868] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90038686 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Osteoporosis 7,751 cases, 476,847 controls NA NR [9886868] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90038656 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Other abdominal problem 6,260 cases, 478,338 controls NA NR [9886868] 0 gastrointestinal disease, Abnormality of the digestive system http://www.ebi.ac.uk/efo/EFO_0010282, http://purl.obolibrary.org/obo/HP_0025031 GCST90038623 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Hypertension 129,909 cases, 354,689 controls NA NR [9886868] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90038604 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Hyperthyroidism or thyrotoxicosis 3,731 cases, 480,867 controls NA NR [9886868] 0 hyperthyroidism http://www.ebi.ac.uk/efo/EFO_0009189 GCST90038636 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Immunological or systemic disorder 41,530 cases, 443,068 controls NA NR [9886868] 0 immune system disease http://www.ebi.ac.uk/efo/EFO_0000540 GCST90038603 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Infection 9,190 cases, 475,408 controls NA NR [9886868] 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90038676 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Inflammatory bowel disease 4,101 cases, 480,497 controls NA NR [9886868] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90038683 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Iron deficiency anemia 2,941 cases, 481,657 controls NA NR [9886868] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90038659 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Irritable bowel syndrome 11,168 cases, 473,430 controls NA NR [9886868] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90038626 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Joint disorder 60,819 cases, 423,779 controls NA NR [9886868] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90038654 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Kidney stone, ureter stone or bladder stone 3,725 cases, 480,873 controls NA NR [9886868] 0 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90038631 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Liver, biliary or pancreas problem 13,495 cases, 471,103 controls NA NR [9886868] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90038622 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Gastroesophageal reflux disease or gastric reflux 20,381 cases, 464,217 controls NA NR [9886868] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90038624 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Gastrointestinal or abdominal disease 77,978 cases, 406,620 controls NA NR [9886868] 0 gastrointestinal disease http://www.ebi.ac.uk/efo/EFO_0010282 GCST90038597 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Nasal or sinus disorder 6,734 cases, 477,864 controls NA NR [9886868] 0 paranasal sinus disease, nasal disorder http://www.ebi.ac.uk/efo/EFO_0009481, http://purl.obolibrary.org/obo/MONDO_0002436 GCST90038670 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Neck injury 3,764 cases, 480,834 controls NA NR [9886868] 0 neck injury http://www.ebi.ac.uk/efo/EFO_0009476 GCST90038700 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Headaches (not migraine) 4,122 cases, 480,476 controls NA NR [9886868] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90038675 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Heart valve problem or heart murmur 3,742 cases, 480,856 controls NA NR [9886868] 0 heart valve disease, Heart murmur http://www.ebi.ac.uk/efo/EFO_0009551, http://purl.obolibrary.org/obo/HP_0030148 GCST90038612 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Hematological disease 7,202 cases, 477,396 controls NA NR [9886868] 0 hematologic disease http://www.ebi.ac.uk/efo/EFO_0005803 GCST90038677 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Hematological or dermatological disease 26,874 cases, 457,724 controls NA NR [9886868] 0 skin disease, hematologic disease http://www.ebi.ac.uk/efo/EFO_0000701, http://www.ebi.ac.uk/efo/EFO_0005803 GCST90038602 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Hepatitis 2,450 cases, 482,148 controls NA NR [9886868] 0 Hepatitis http://purl.obolibrary.org/obo/HP_0012115 GCST90038627 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Hiatus hernia 10,810 cases, 473,788 controls NA NR [9886868] 0 Hiatus hernia http://purl.obolibrary.org/obo/HP_0002036 GCST90038691 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. High cholesterol 59,853 cases, 424,745 controls NA NR [9886868] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90038690 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Other joint disorder 4,698 cases, 479,900 controls NA NR [9886868] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90038688 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Other neurological problem 6,863 cases, 477,735 controls NA NR [9886868] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90038674 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Hypothyroidism or myxedema 23,497 cases, 461,101 controls NA NR [9886868] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90038637 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Other renal or kidney problem 2,609 cases, 481,989 controls NA NR [9886868] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90038666 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Other respiratory problems 5,283 cases, 479,315 controls NA NR [9886868] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90038618 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Peripheral nerve disorder 2,595 cases, 482,003 controls NA NR [9886868] 0 peripheral neuropathy http://www.ebi.ac.uk/efo/EFO_0003100 GCST90038643 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Pneumonia 6,666 cases, 477,932 controls NA NR [9886868] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90038665 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Prolapsed or slipped disc 7,987 cases, 476,611 controls NA NR [9886868] 0 vertebral disorder http://purl.obolibrary.org/obo/MONDO_0045002 GCST90038658 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Psoriasis 5,427 cases, 479,171 controls NA NR [9886868] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90038681 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Psychological or psychiatric problem 36,199 cases, 448,399 controls NA NR [9886868] 0 psychiatric disorder http://purl.obolibrary.org/obo/MONDO_0002025 GCST90038641 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Pulmonary embolism with or without deep venous thrombosis 3,940 cases, 480,658 controls NA NR [9886868] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90038614 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Renal or urological disease 22,855 cases, 461,743 controls NA NR [9886868] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90038598 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Respiratory infection 6,803 cases, 477,795 controls NA NR [9886868] 0 respiratory tract infectious disorder http://purl.obolibrary.org/obo/MONDO_0024355 GCST90038701 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Migraine 13,971 cases, 470,627 controls NA NR [9886868] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90038646 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Chronic sinusitis 3,014 cases, 481,584 controls NA NR [9886868] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90038673 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Connective tissue disorder 3,206 cases, 481,392 controls NA NR [9886868] 0 connective tissue disease http://www.ebi.ac.uk/efo/EFO_1001986 GCST90038660 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Appendicitis 4,089 cases, 480,509 controls NA NR [9886868] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90038695 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Depression 27,568 cases, 457,030 controls NA NR [9886868] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90038650 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Dermatologic disease 20,101 cases, 464,497 controls NA NR [9886868] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90038679 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Bacterial infection 4,920 cases, 479,678 controls NA NR [9886868] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90038709 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Bladder problem (not cancer) 4,549 cases, 480,049 controls NA NR [9886868] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90038632 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Bone disorder 10,730 cases, 473,868 controls NA NR [9886868] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90038652 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Bowel problem 31,766 cases, 452,832 controls NA NR [9886868] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90038621 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Bronchitis 3,510 cases, 481,088 controls NA NR [9886868] 0 bronchitis http://www.ebi.ac.uk/efo/EFO_0009661 GCST90038668 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Disc problem 9,190 cases, 475,408 controls NA NR [9886868] 0 vertebral disorder http://purl.obolibrary.org/obo/MONDO_0045002 GCST90038697 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Cardiovascular disease 177,923 cases, 306,675 controls NA NR [9886868] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90038595 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Cataracts 7,038 cases, 477,560 controls NA NR [9886868] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90038649 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Cerebrovascular disease 8,915 cases, 475,683 controls NA NR [9886868] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90038606 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Esophageal disorder 31,526 cases, 453,072 controls NA NR [9886868] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90038619 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Cholelithiasis or gall stones 7,895 cases, 476,703 controls NA NR [9886868] 0 cholelithiasis, gallstones http://www.ebi.ac.uk/efo/EFO_0004799, http://www.ebi.ac.uk/efo/EFO_0004210 GCST90038629 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Eye or eyelid problem 19,915 cases, 464,683 controls NA NR [9886868] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90038640 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Chronic or degenerative neurological problem 2,960 cases, 481,638 controls NA NR [9886868] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90038644 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Fractures 8,844 cases, 475,754 controls NA NR [9886868] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90038703 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Fracture of forearm or wrist 2,291 cases, 482,307 controls NA NR [9886868] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90038705 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Fracture of lower leg or ankle 2,594 cases, 482,004 controls NA NR [9886868] 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90038707 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Fracture of pelvis or lower limb 4,080 cases, 480,518 controls NA NR [9886868] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90038706 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Fracture of upper limb or shoulder 4,335 cases, 480,263 controls NA NR [9886868] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90038704 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Gallbladder disease 8,587 cases, 476,011 controls NA NR [9886868] 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90038628 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Abdominal hernia 2,800 cases, 481,798 controls NA NR [9886868] 0 Hernia of the abdominal wall http://purl.obolibrary.org/obo/HP_0004299 GCST90038696 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Allergy, hypersensitivity or anaphylaxis 35,890 cases, 448,708 controls NA NR [9886868] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90038661 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Anemia 5,259 cases, 479,339 controls NA NR [9886868] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90038678 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Angina 15,527 cases, 469,071 controls NA NR [9886868] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90038609 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Anxiety or panic attacks 6,514 cases, 478,084 controls NA NR [9886868] 0 anxiety, panic disorder http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004262 GCST90038651 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Deep venous thrombosis 9,529 cases, 475,069 controls NA NR [9886868] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90038615 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Arrhythmia 7,207 cases, 477,391 controls NA NR [9886868] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90038611 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Arthritis (not osteoarthritis) 3,777 cases, 480,821 controls NA NR [9886868] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90038699 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Asthma 56,087 cases, 428,511 controls NA NR [9886868] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90038616 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Atrial fibrillation 3,537 cases, 481,061 controls NA NR [9886868] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90038689 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Back pain 2,866 cases, 481,732 controls NA NR [9886868] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90038698 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Back problem 28,856 cases, 455,742 controls NA NR [9886868] 0 vertebral column disorder http://purl.obolibrary.org/obo/MONDO_0000812 GCST90038653 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Diabetes 24,659 cases, 459,939 controls NA NR [9886868] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90038633 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Diabetes or endocrine disease 51,949 cases, 432,649 controls NA NR [9886868] 0 endocrine system disease, diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0001379, http://www.ebi.ac.uk/efo/EFO_0000400 GCST90038599 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Cardiac problem 34,616 cases, 449,982 controls NA NR [9886868] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90038605 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Diverticular disease 5,218 cases, 479,380 controls NA NR [9886868] 0 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90038682 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Drug allergy or anaphylactic reaction 4,133 cases, 480,465 controls NA NR [9886868] 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90038663 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Ear disorder 7,134 cases, 477,464 controls NA NR [9886868] 0 disorder of ear http://purl.obolibrary.org/obo/MONDO_0021205 GCST90038672 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Ear-nose-throat disorder 17,317 cases, 467,281 controls NA NR [9886868] 0 otorhinolaryngologic disease http://purl.obolibrary.org/obo/MONDO_0024623 GCST90038669 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Eczema or dermatitis 12,176 cases, 472,422 controls NA NR [9886868] 0 Eczema, dermatitis http://purl.obolibrary.org/obo/HP_0000964, http://purl.obolibrary.org/obo/MONDO_0002406 GCST90038680 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Emphysema or chronic bronchitis 10,174 cases, 474,424 controls NA NR [9886868] 0 emphysema, chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0000464, http://www.ebi.ac.uk/efo/EFO_0006505 GCST90038617 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Epilepsy 3,900 cases, 480,698 controls NA NR [9886868] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90038645 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Cervical spondylosis 3,352 cases, 481,246 controls NA NR [9886868] 0 cervical spondylosis http://www.ebi.ac.uk/efo/EFO_0009610 GCST90038693 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Essential hypertension 2,287 cases, 482,311 controls NA NR [9886868] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90038608 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Chronic fatigue syndrome 2,092 cases, 482,506 controls NA NR [9886868] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90038694 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Food allergy or anaphylactic reaction 2,185 cases, 482,413 controls NA NR [9886868] 0 food allergy http://www.ebi.ac.uk/efo/EFO_1001890 GCST90038662 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Respiratory or ear-nose-throat disease 86,427 cases, 398,171 controls NA NR [9886868] 0 otorhinolaryngologic disease http://purl.obolibrary.org/obo/MONDO_0024623 GCST90038596 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Retinal problem 2,902 cases, 481,696 controls NA NR [9886868] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90038647 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Rheumatoid arthritis 5,427 cases, 479,171 controls NA NR [9886868] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90038685 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Sciatica 4,549 cases, 480,049 controls NA NR [9886868] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90038692 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Spine arthritis or spondylitis 4,113 cases, 480,485 controls NA NR [9886868] 0 vertebral column disorder http://purl.obolibrary.org/obo/MONDO_0000812 GCST90038657 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Stomach disorder 5,454 cases, 479,144 controls NA NR [9886868] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90038620 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Stroke 6,925 cases, 477,673 controls NA NR [9886868] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90038613 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Throat or larynx disorder 3,945 cases, 480,653 controls NA NR [9886868] 0 laryngeal disease, throat disease http://www.ebi.ac.uk/efo/EFO_0009673, http://www.ebi.ac.uk/efo/EFO_0009479 GCST90038671 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Thyroid problem (not cancer) 28,254 cases, 456,344 controls NA NR [9886868] 0 thyroid disease http://www.ebi.ac.uk/efo/EFO_1000627 GCST90038635 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Tonsillitis 3,300 cases, 481,298 controls NA NR [9886868] 0 pharyngitis http://purl.obolibrary.org/obo/MONDO_0002258 GCST90038702 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Tuberculosis 2,473 cases, 482,125 controls NA NR [9886868] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90038710 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Type 2 diabetes 3,260 cases, 481,338 controls NA NR [9886868] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90038634 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Ulcerative colitis 2,515 cases, 482,083 controls NA NR [9886868] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90038684 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Urinary tract or kidney infection 2,691 cases, 481,907 controls NA NR [9886868] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90038630 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Venous thromboembolism 12,240 cases, 472,358 controls NA NR [9886868] 0 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90038607 Genome-wide genotyping array 2021-11-12 33959723 Donertas HM 2021-04-08 Nat Aging www.ncbi.nlm.nih.gov/pubmed/33959723 Common genetic associations between age-related diseases. Viral infection 3,839 cases, 480,759 controls NA NR [9886868] 0 viral disease http://www.ebi.ac.uk/efo/EFO_0000763 GCST90038708 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 1) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90044778 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 2) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90044779 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 3) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90044780 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 4) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044781 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 5) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044782 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 6) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044783 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 7) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lip morphology measurement, eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845, http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044784 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 8) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90044785 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 9) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044786 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 10) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044787 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 11) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044788 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 12) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044789 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 13) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044790 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 14) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044791 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 15) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90044792 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 16) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90044793 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 17) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90044794 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 18) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044795 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 19) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044796 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 20) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST90044797 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 21) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044798 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 22) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044799 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 23) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044800 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 24) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044801 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 25) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044802 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 26) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044803 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 27) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044804 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 28) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044805 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 29) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044806 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 30) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90044807 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 31) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90044808 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 32) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90044809 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 33) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90044810 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 34) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90044811 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 35) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST90044812 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 36) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044813 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 37) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044814 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 38) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044815 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 39) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90044816 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 40) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST90044817 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 41) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST90044818 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 42) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044819 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 43) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044820 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 44) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044821 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 45) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044822 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 46) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044823 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 47) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90044824 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 48) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044825 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 49) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044826 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 50) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044827 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 51) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044828 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 52) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044829 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 53) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044830 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 54) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044831 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 55) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90044832 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 56) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044833 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 57) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044834 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 58) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044835 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 59) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 1 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90044836 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 60) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90044837 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 61) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90044838 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 62) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90044839 Genome-wide genotyping array 2021-11-15 34411106 Liu C 2021-08-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34411106 Genome scans of facial features in East Africans and cross-population comparisons reveal novel associations. Facial morphology (segment 63) 2,595 Tanzanian ancestry individuals NA Illumina [NR] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90044840 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Anterior lobe of cerebellar volume (including I to V lobules) 33,251 European ancestry individuals NA Affymetrix [6193476] (imputed) 0 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020191 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Superior Posterior lobe of cerebellar volume (including VI to Crus I hemispheric lobules) 33,251 European ancestry individuals NA Affymetrix [6193476] (imputed) 0 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020192 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Superior Posterior lobe of cerebellar volume (including VI to Crus I vermal lobules, excluding Crus I vermis) 33,251 European ancestry individuals NA Affymetrix [6193476] (imputed) 0 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020193 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Inferior Posterior lobe of cerebellar volume (including Crus II to IX hemispheric lobules) 33,251 European ancestry individuals NA Affymetrix [6193476] (imputed) 0 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020194 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Inferior Posterior lobe of cerebellar volume (including Crus II to IX vermal lobules) 33,251 European ancestry individuals NA Affymetrix [6193476] (imputed) 0 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020195 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Flocculonodular lobe of cerebellar volume (including X hemispheric lobules) 33,251 European ancestry individuals NA Affymetrix [6193476] (imputed) 0 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020196 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Flocculonodular lobe of cerebellar volume (including X vermal lobules) 33,251 European ancestry individuals NA Affymetrix [6193476] (imputed) 0 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020197 Genome-wide genotyping array 2022-02-14 35079123 Chambers T 2022-01-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35079123 Genetic common variants associated with cerebellar volume and their overlap with mental disorders: a study on 33,265 individuals from the UK-Biobank. Total cerebellar volume (excluding Crus I vermis) 33,265 European ancestry individuals NA Affymetrix [6193476] (imputed) 33 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90020190 Genome-wide genotyping array 2022-02-04 35047858 Polikowsky HG 2021-12-02 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35047858 Population-based genetic effects for developmental stuttering. Developmental stuttering 250 African ancestry cases, 1,910 African ancestry controls, 160 Hispanic ancestry cases, 1,186 Hispanic ancestry controls, 42 East Asian ancestry cases, 113 East Asian ancestry controls, 1,565 European ancestry cases, 10,434 European ancestry controls, 44 South Asian ancestry cases, 143 South Asian ancestry controls, 4 Native American ancestry cases, 32 Native American ancestry controls, 44 Asian ancestry cases, 404 Asian ancestry controls, 21 cases, 109 controls NA Illumina [7275796] (imputed) 16 Stuttering http://purl.obolibrary.org/obo/HP_0025268 GCST90085698 Genome-wide genotyping array 2022-02-22 35131881 Testori A 2022-02-07 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/35131881 Genetic analysis in African American children supports ancestry specific neuroblastoma susceptibility. Neuroblastoma 629 African American cases, 2,990 African American controls NA Illumina [8524982] (imputed) 29 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST90094905 Genome-wide genotyping array 2022-02-22 35131881 Testori A 2022-02-07 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/35131881 Genetic analysis in African American children supports ancestry specific neuroblastoma susceptibility. Neuroblastoma 254 African American cases, 2,990 African American controls NA Illumina [NR] (imputed) 36 neuroblastoma http://www.ebi.ac.uk/efo/EFO_0000621 GCST90094906 Genome-wide genotyping array 2022-02-18 34520856 Han X 2021-09-11 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/34520856 Identification of novel loci influencing refractive error in East Asian populations using an extreme phenotype design. Spherical equivalent 1,852 Chinese Han ancestry individuals 3,538 Chinese ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST90094875 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:1_[M+H]1+/Phosphatidylethanolamine_39:1_[M+H]1+/Phosphatidate_41:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060360 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:2_[M+H]1+/Phosphatidylethanolamine_39:2_[M+H]1+/Phosphatidate_41:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060354 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:2_[M+OAc]1-/Phosphatidylserine_40:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060465 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:3_[M+H]1+/Phosphatidylethanolamine_39:3_[M+H]1+/Phosphatidate_41:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 36 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060349 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:3_[M+OAc]1-/Phosphatidylserine_40:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060462 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:4_[M+OAc]1-/Phosphatidylserine_40:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060459 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:5_[M+H]1+/Phosphatidylethanolamine_39:5_[M+H]1+/Phosphatidate_41:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060345 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:5_[M+OAc]1-/Phosphatidylserine_40:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060456 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:6_[M+H]1+/Phosphatidylethanolamine_39:6_[M+H]1+/Phosphatidate_41:7_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060341 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:6_[M+OAc]1-/Phosphatidylserine_40:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060450 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:7_[M+OAc]1-/Phosphatidylserine_40:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060445 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_37:3_[M+OAc]1-/Phosphatidylserine_41:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 28 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060487 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_37:4_[M+H]1+/Phosphatidylethanolamine_40:4_[M+H]1+/Phosphatidate_42:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 36 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060378 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_37:4_[M+OAc]1-/Phosphatidylserine_41:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060485 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_37:5_[M+H]1+/Phosphatidylethanolamine_40:5_[M+H]1+/Phosphatidate_42:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060374 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_37:5_[M+OAc]1-/Phosphatidylserine_41:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060481 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_37:6_[M+H]1+/Phosphatidylethanolamine_40:6_[M+H]1+/Phosphatidate_42:7_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060371 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_37:6_[M+OAc]1-/Phosphatidylserine_41:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060474 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:2_[M+H]1+/Phosphatidylethanolamine_41:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 35 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060408 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:3_[M+H]1+/Phosphatidylethanolamine_41:3_[M+H]1+/Phosphatidate_43:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 37 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060402 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:4_[M+OAc]1-/Phosphatidylserine_42:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060503 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:5_[M+H]1+/Phosphatidylethanolamine_41:5_[M+H]1+/Phosphatidate_43:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 39 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060395 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:6_[M+H]1+/Phosphatidylethanolamine_41:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 14 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060393 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:6_[M+OAc]1-/Phosphatidylserine_42:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060499 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:7_[M+OAc]1-/Phosphatidylserine_42:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060496 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_18:0_[M+H]1+/Lysophosphatidylethanolamine_21:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 9 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060163 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_18:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060183 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_18:1_[M+H]1+/Phosphatidylcholine-P_18:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060160 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_18:1_[M+OAc]1-/Phosphatidylcholine-P_18:0_[M+OAc]1-/Lysophosphatidylserine_22:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060182 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_30:1_[M+H]1+/Phosphatidylcholine-P_30:0_[M+H]1+/Phosphatidylethanolamine-O_33:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 22 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060230 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_31:0_[M+H]1+/Phosphatidylethanolamine-O_34:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060243 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_31:2_[M+H]1+/Phosphatidylcholine-P_31:1_[M+H]1+/Phosphatidylethanolamine-O_34:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060237 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_32:0_[M+H]1+/Phosphatidylethanolamine-O_35:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060255 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_32:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060344 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_32:1_[M+H]1+/Phosphatidylcholine-P_32:0_[M+H]1+/Phosphatidylethanolamine-O_35:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 53 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060254 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_32:1_[M+OAc]1-/Phosphatidylcholine-P_32:0_[M+OAc}1-/Phosphatidylserine-O_36:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060338 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_33:3_[M+H]1+/Phosphatidylcholine-P_33:2_[M+H]1+/Phosphatidylethanolamine-O_36:3_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 11 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060261 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_33:3_[M+OAc]1-/Phosphatidylcholine-P_33:2_[M+OAc]1-/Phosphatidylserine-O_37:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060353 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_34:1_[M+H]1+/Phosphatidylcholine-P_34:0_[M+H]1+/Phosphatidylethanolamine-O_37:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 36 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060284 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_34:1_[M+OAc]1-/Phosphatidylcholine-P_34:0_[M+OAc]1-/Phosphatidylserine-O_38:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060392 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_34:2_[M+H]1+/Phosphatidylcholine-P_34:1_[M+H]1+/Phosphatidylethanolamine-O_37:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060280 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_34:2_[M+OAc]1-/Phosphatidylcholine-P_34:1_[M+OAc]1-/Phosphatidylserine-O_38:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060389 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_34:3_[M+H]1+/Phosphatidylcholine-P_34:2_[M+H]1+/Phosphatidylethanolamine-P_37:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060277 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_34:3_[M+OAc]1-/Phosphatidylcholine-P_34:2_[M+OAc]1-/Phosphatidylserine-O_38:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060384 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_34:4_[M+OAc]1-/Phosphatidylcholine-P_34:3_[M+OAc]1-/Phosphatidylserine-O_38:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060382 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_35:1_[M+H]1+/Phosphatidylcholine-P_35:0_[M+H]1+/Phosphatidylethanolamine-O_38:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060308 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_35:3_[M+OAc]1-/Phosphatidylcholine-P_35:2_[M+OAc]1-/Phosphatidylserine-P_39:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060407 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_35:4_[M+OAc]1-/Phosphatidylcholine-P_35:3_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060401 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_36:1_[M+H]1+/Phosphatidylcholine-P_36:0_[M+H]1+/Phosphatidylethanolamine-O_39:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 27 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060332 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_36:2_[M+H]1+/Phosphatidylcholine-P_36:1_[M+H]1+/Phosphatidylethanolamine-P_39:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 10 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060326 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:8_[M+OAc]1-/Phosphatidylserine_42:7_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060493 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_38:9_[M+OAc]1-/Phosphatidylserine_42:8_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060490 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_39:6_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060512 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_39:7_[M+H]1+/Phosphatidylethanolamine_42:7_[M+H]1+/Phosphatidate_44:8_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060414 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:10_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060519 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:4_[M+H]1+/Phosphatidylethanolamine_43:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 26 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060457 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:4_[M+OAc]1-/Phosphatidylserine_44:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060537 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:5_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 31 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060451 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:6_[M+H]1+/Phosphatidylethanolamine_43:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 22 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060446 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:6_[M+OAc]1-/Phosphatidylserine_44:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 19 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060534 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:7_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060442 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:7_[M+OAc]1-/Phosphatidylserine_44:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060530 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:8_[M+OAc]1-/Phosphatidylserine_44:7_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060526 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_40:9_[M+OAc]1-/Phosphatidylserine_44:8_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060523 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_41:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060549 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_42:4_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060552 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_43:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060527 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_43:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060560 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_43:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060558 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_44:5_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 17 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060563 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_46:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060567 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_52:4_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060091 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-2O_32:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 19 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060244 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_16:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060171 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O_17:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060176 Genome-wide genotyping array 2022-01-04 34116867 Tanaka N 2021-06-02 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34116867 Eight novel susceptibility loci and putative causal variants in atopic dermatitis. Atopic dermatitis 2,597 Japanese ancestry cases, 110,504 Japanese ancestry controls NA Illumina [9900441] (imputed) 17 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90086148 Genome-wide genotyping array 2022-01-04 34116867 Tanaka N 2021-06-02 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34116867 Eight novel susceptibility loci and putative causal variants in atopic dermatitis. Atopic dermatitis 2,597 Japanese ancestry cases, 110,504 Japanese ancestry controls, 25,685 European ancestry cases, 76,768 European ancestry controls NA Illumina [5170515] (imputed) 39 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90086149 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ibuprofen (Gene-based burden) 56,585 European ancestry cases, 264,173 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082050 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 5 (UKB data field 21036) 5,756 European ancestry cases, 39,185 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078737 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urinary albumin-to-creatinine ratio 126,399 European ancestry individuals NA Affymetrix, Illumina [222188] 2 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST90081533 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching completion status - Completed (UKB data field 20244) (Gene-based burden) 98,337 European ancestry cases, 7,064 European ancestry controls NA Illumina [165792] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082364 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.7: Personal history of (corrected) congenital malformations 524 European ancestry cases, 387,359 European ancestry controls NA Affymetrix, Illumina [219494] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081374 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching completion status - Completed with pause (UKB data field 20244) (Gene-based burden) 3,780 European ancestry cases, 101,621 European ancestry controls NA Illumina [165792] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082366 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Light smokers - at least 100 smokes in lifetime (UKB data field 2644) 55,456 European ancestry cases, 64,128 European ancestry controls NA Affymetrix, Illumina [211924] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078954 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Part of a multiple birth (UKB data field 1777) (Gene-based burden) 9,475 European ancestry cases, 414,637 European ancestry controls NA Illumina [185844] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90081598 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever worried more than most people would in similar situation (UKB data field 20425) 30,487 European ancestry cases, 86,633 European ancestry controls NA Affymetrix, Illumina [209048] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078442 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Past tobacco smoking - I have never smoked (UKB data field 1249) (Gene-based burden) 171,084 European ancestry cases, 226,005 European ancestry controls NA Illumina [185414] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90081572 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Back pain for three months (UKB data field 3571) 79,056 European ancestry cases, 35,975 European ancestry controls NA Affymetrix, Illumina [205633] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90079063 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Past tobacco smoking - Smoked on most or all days (UKB data field 1249) (Gene-based burden) 109,016 European ancestry cases, 288,073 European ancestry controls NA Illumina [185414] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90081571 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measures duration (UKB data field 5198) 110,881 European ancestry individuals NA Affymetrix, Illumina [200331] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90079329 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peak expiratory flow (UKB data field 3064) (Gene-based burden) 395,451 European ancestry individuals NA Illumina [185485] 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90083005 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye surgery ever - Yes but more than 4 weeks ago (UKB data field 5181) 8,594 European ancestry cases, 102,287 European ancestry controls NA Affymetrix, Illumina [200331] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90079322 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Phosphate levels (UKB data field 30810) (Gene-based burden) 377,669 European ancestry individuals NA Illumina [185101] 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90083023 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye surgery ever - Possibly but more than 4 weeks ago (UKB data field 5181) 651 European ancestry cases, 110,230 European ancestry controls NA Affymetrix, Illumina [200331] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90079323 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Platelet count (UKB data field 30080) (Gene-based burden) 419,189 European ancestry individuals NA Illumina [185803] 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90082973 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Current eye infection (UKB data field 5183) 1,271 European ancestry cases, 109,604 European ancestry controls NA Affymetrix, Illumina [200327] 0 eye infectious disorder http://purl.obolibrary.org/obo/MONDO_0043885 GCST90079324 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Platelet crit (UKB data field 30090) (Gene-based burden) 419,060 European ancestry individuals NA Illumina [185803] 0 platelet crit http://www.ebi.ac.uk/efo/EFO_0007985 GCST90082974 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration visual acuity screen displayed right (UKB data field 5186) 110,647 European ancestry individuals NA Affymetrix, Illumina [200000] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90079325 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Platelet distribution width (UKB data field 30110) (Gene-based burden) 419,059 European ancestry individuals NA Illumina [185803] 0 platelet component distribution width http://www.ebi.ac.uk/efo/EFO_0007984 GCST90082976 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration visual acuity screen displayed left (UKB data field 5188) 110,648 European ancestry individuals NA Affymetrix, Illumina [199995] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90079326 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - final answer - Grey cross (UKB data field 4293) (Gene-based burden) 3,159 European ancestry cases, 172,724 European ancestry controls NA Illumina [176981] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90083159 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - Number of letters correct in round right (UKB data field 5076) 110,269 European ancestry individuals NA Affymetrix, Illumina [199415] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90079265 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 4 (UKB data field 21040) (Gene-based burden) 7,543 European ancestry cases, 146,880 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082755 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian angle right (UKB data field 5107) 103,540 European ancestry individuals NA Affymetrix, Illumina [189235] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079285 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 5 (UKB data field 21040) (Gene-based burden) 18,335 European ancestry cases, 136,088 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082756 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian right (UKB data field 5132) 103,540 European ancestry individuals NA Affymetrix, Illumina [189235] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079298 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 6 (UKB data field 21040) (Gene-based burden) 9,480 European ancestry cases, 144,943 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082757 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian angle right (UKB data field 5100) 103,540 European ancestry individuals NA Affymetrix, Illumina [189235] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079278 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 7 (UKB data field 21040) (Gene-based burden) 11,287 European ancestry cases, 143,136 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082758 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian right (UKB data field 5099) 103,540 European ancestry individuals NA Affymetrix, Illumina [189235] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079276 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 8 (UKB data field 21040) (Gene-based burden) 8,837 European ancestry cases, 145,586 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082759 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm right 103,540 European ancestry individuals NA Affymetrix, Illumina [189235] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081480 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 9 (UKB data field 21040) (Gene-based burden) 4,696 European ancestry cases, 149,727 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082760 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power angle right (UKB data field 5115) 103,530 European ancestry individuals NA Affymetrix, Illumina [189218] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079293 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 0 - Very happy (UKB data field 21040) (Gene-based burden) 29,522 European ancestry cases, 124,901 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082750 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neck/shoulder pain for three months (UKB data field 3404) 71,753 European ancestry cases, 31,678 European ancestry controls NA Affymetrix, Illumina [187759] 0 Shoulder pain http://purl.obolibrary.org/obo/HP_0030834 GCST90079054 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 10 - Very unhappy (UKB data field 21040) (Gene-based burden) 4,995 European ancestry cases, 149,428 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082751 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching - Time to complete round (UKB data field 20133) 102,772 European ancestry individuals NA Affymetrix, Illumina [187600] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078314 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seated height (UKB data field 51) (Gene-based burden) 430,080 European ancestry individuals NA Illumina [185928] 0 sitting height measurement http://www.ebi.ac.uk/efo/EFO_0011011 GCST90083316 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interval between previous point and current one in numeric path trail 1 (UKB data field 20149) 102,460 European ancestry individuals NA Affymetrix, Illumina [187182] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078315 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seen doctor for nerves anxiety tension or depression (UKB data field 2090) (Gene-based burden) 150,752 European ancestry cases, 277,276 European ancestry controls NA Illumina [185897] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90082669 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index for irregular astigmatism level right - doubtful (UKB data field 5164) 4,583 European ancestry cases, 97,024 European ancestry controls NA Affymetrix, Illumina [186196] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079320 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seen psychiatrist for nerves anxiety tension or depression (UKB data field 2100) (Gene-based burden) 51,158 European ancestry cases, 377,832 European ancestry controls NA Illumina [185905] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90082672 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index for irregular astigmatism level right - high possibility abnormality (UKB data field 5164) 4,456 European ancestry cases, 97,151 European ancestry controls NA Affymetrix, Illumina [186196] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079321 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Self harmed in past year (UKB data field 20481) (Gene-based burden) 523 European ancestry cases, 5,507 European ancestry controls NA Illumina [57911] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90082499 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index for irregular astigmatism level right - normal (UKB data field 5164) 97,932 European ancestry cases, 3,675 European ancestry controls NA Affymetrix, Illumina [186196] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079319 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Basal cell carcinoma (UKB data field 20001) (Gene-based burden) 4,723 European ancestry cases, 34,891 European ancestry controls NA Illumina [134284] 0 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90081626 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 16 (20165) 1,166 European ancestry cases, 108,320 European ancestry controls NA Affymetrix, Illumina [197769] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078329 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory result - Correct recall on first attempt (UKB data field 20018) (Gene-based burden) 141,954 European ancestry cases, 34,246 European ancestry controls NA Illumina [177015] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90082233 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - adult (UKB data field 20169) 91,437 European ancestry cases, 18,036 European ancestry controls NA Affymetrix, Illumina [197756] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078334 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory result - Correct recall on second attempt (UKB data field 20018) (Gene-based burden) 29,799 European ancestry cases, 146,401 European ancestry controls NA Illumina [177015] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90082234 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - develop (UKB data field 20169) 7,762 European ancestry cases, 101,711 European ancestry controls NA Affymetrix, Illumina [197756] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078333 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory result - Instruction not recalled either skipped or incorrect (UKB data field 20018) (Gene-based burden) 8,070 European ancestry cases, 168,130 European ancestry controls NA Illumina [177015] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90082232 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - grow (UKB data field 20169) 10,072 European ancestry cases, 99,401 European ancestry controls NA Affymetrix, Illumina [197756] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078332 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse rate (UKB data field 4194) (Gene-based burden) 173,103 European ancestry individuals NA Illumina [176817] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90083146 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 5 (UKB data field 20171) 5,923 European ancestry cases, 103,014 European ancestry controls NA Affymetrix, Illumina [196956] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078335 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse rate automated reading (UKB data field 102) (Gene-based burden) 408,215 European ancestry individuals NA Illumina [185723] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90081546 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 6 (UKB data field 20171) 96,930 European ancestry cases, 12,007 European ancestry controls NA Affymetrix, Illumina [196956] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078336 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse wave Arterial Stiffness index (UKB data field 21021) (Gene-based burden) 172,449 European ancestry individuals NA Illumina [176742] 0 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST90082673 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 7 (UKB data field 20171) 781 European ancestry cases, 108,156 European ancestry controls NA Affymetrix, Illumina [196956] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078337 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse wave peak to peak time (UKB data field 4196) (Gene-based burden) 173,016 European ancestry individuals NA Illumina [176804] 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90083148 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 8 (UKB data field 20171) 1,587 European ancestry cases, 107,350 European ancestry controls NA Affymetrix, Illumina [196956] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078338 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse wave reflection index (UKB data field 4195) (Gene-based burden) 173,103 European ancestry individuals NA Illumina [176817] 0 pulse wave reflection index measurement http://www.ebi.ac.uk/efo/EFO_0009804 GCST90083147 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 9 (UKB data field 20171) 3,716 European ancestry cases, 105,221 European ancestry controls NA Affymetrix, Illumina [196956] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078339 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rheumatoid arthritis (Gene-based burden) 8,561 European ancestry cases, 295,029 European ancestry controls NA Illumina [183537] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90085490 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type of tobacco previously smoked - Cigars or pipes (UKB data field 2877) 5,039 European ancestry cases, 103,837 European ancestry controls NA Affymetrix, Illumina [195844] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078968 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - More than half the days (UKB data field 20518) (Gene-based burden) 1,124 European ancestry cases, 138,348 European ancestry controls NA Illumina [172116] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90082589 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type of tobacco previously smoked - Hand rolled cigarettes (UKB data field 2877) 7,435 European ancestry cases, 101,441 European ancestry controls NA Affymetrix, Illumina [195844] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078967 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - Nearly every day (UKB data field 20518) (Gene-based burden) 857 European ancestry cases, 138,615 European ancestry controls NA Illumina [172116] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90082590 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type of tobacco previously smoked - Manufactured cigarettes (UKB data field 2877) 96,924 European ancestry cases, 11,952 European ancestry controls NA Affymetrix, Illumina [195844] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078966 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - Not at all (UKB data field 20518) (Gene-based burden) 131,513 European ancestry cases, 7,959 European ancestry controls NA Illumina [172116] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90082587 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - imigran (Gene-based burden) 747 European ancestry cases, 320,011 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082128 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent worrying too much about different things - Several days (UKB data field 20520) (Gene-based burden) 37,314 European ancestry cases, 101,813 European ancestry controls NA Illumina [172049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082594 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure corneal compensated left (UKB data field 5262) 105,697 European ancestry individuals NA Affymetrix, Illumina [192579] 1 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90079337 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Red blood cell erythrocyte count (UKB data field 30010) (Gene-based burden) 419,193 European ancestry individuals NA Illumina [185803] 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90082965 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure Goldmann correlated left (UKB data field 5263) 105,697 European ancestry individuals 34,386 European ancestry individuals Affymetrix, Illumina [192579] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90079338 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Red blood cell erythrocyte distribution width (UKB data field 30070) (Gene-based burden) 419,192 European ancestry individuals NA Illumina [185803] 0 Red cell distribution width http://www.ebi.ac.uk/efo/EFO_0009188 GCST90082972 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Likelihood of resuming smoking - No definitely not (UKB data field 2936) 94,791 European ancestry cases, 11,787 European ancestry controls NA Affymetrix, Illumina [192396] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078973 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Refractive astigmatism (Gene-based burden) 106,495 European ancestry individuals NA Illumina [167325] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90085492 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Likelihood of resuming smoking - No probably not (UKB data field 2936) 11,048 European ancestry cases, 95,530 European ancestry controls NA Affymetrix, Illumina [192396] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078972 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Refractive astigmatism (first instance) (Gene-based burden) 93,186 European ancestry individuals NA Illumina [164300] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90085491 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Likelihood of resuming smoking probably (UKB data field 2936) 1,432 European ancestry cases, 105,146 European ancestry controls NA Affymetrix, Illumina [192396] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078971 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Refractive astigmatism - started wearing glasses contacts before 40 (Gene-based burden) 48,482 European ancestry individuals NA Illumina [143543] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90085493 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit substitution - Duration to entering value (UKB data field 20230) 105,636 European ancestry individuals NA Affymetrix, Illumina [192065] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078374 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age of first facial hair - About average age (UKB data field 2375) (Gene-based burden) 154,111 European ancestry cases, 36,815 European ancestry controls NA Illumina [176907] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90082925 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit substitution - Values entered (UKB data field 20229) 105,636 European ancestry individuals NA Affymetrix, Illumina [192065] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078373 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age of first facial hair - Older than average (UKB data field 2375) (Gene-based burden) 25,253 European ancestry cases, 165,673 European ancestry controls NA Illumina [176907] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90082926 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching completion status - Abandoned (UKB data field 20244) 3,284 European ancestry cases, 102,117 European ancestry controls NA Affymetrix, Illumina [191705] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078379 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age of first facial hair - Younger than average (UKB data field 2375) (Gene-based burden) 13,051 European ancestry cases, 177,875 European ancestry controls NA Illumina [176907] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90082924 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching completion status - Completed (UKB data field 20244) 98,337 European ancestry cases, 7,064 European ancestry controls NA Affymetrix, Illumina [191705] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078378 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age voice broke - About average age (UKB data field 2385) (Gene-based burden) 164,496 European ancestry cases, 18,349 European ancestry controls NA Illumina [176148] 0 age at voice drop http://www.ebi.ac.uk/efo/EFO_0007888 GCST90082928 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching completion status - Completed with pause (UKB data field 20244) 3,780 European ancestry cases, 101,621 European ancestry controls NA Affymetrix, Illumina [191705] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078380 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age voice broke - Older than average (UKB data field 2385) (Gene-based burden) 11,123 European ancestry cases, 171,722 European ancestry controls NA Illumina [176148] 0 age at voice drop http://www.ebi.ac.uk/efo/EFO_0007888 GCST90082929 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Bipolar I Disorder (UKB data field 20126) 673 European ancestry cases, 103,157 European ancestry controls NA Affymetrix, Illumina [191544] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90078309 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Relative age voice broke - Younger than average (UKB data field 2385) (Gene-based burden) 8,108 European ancestry cases, 174,737 European ancestry controls NA Illumina [176148] 0 age at voice drop http://www.ebi.ac.uk/efo/EFO_0007888 GCST90082927 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Bipolar II Disorder (UKB data field 20126) 623 European ancestry cases, 103,207 European ancestry controls NA Affymetrix, Illumina [191544] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90078310 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - A little bit (UKB data field 20497) (Gene-based burden) 28,097 European ancestry cases, 111,415 European ancestry controls NA Illumina [172118] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90082532 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking cessation (age of onset) (UKB data field 2897) 108,447 European ancestry individuals NA Affymetrix, Illumina [195181] 0 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST90078969 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of tiredness or low energy - More than half the days (UKB data field 20519) (Gene-based burden) 7,684 European ancestry cases, 131,738 European ancestry controls NA Illumina [172112] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082592 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High blood pressure (age of onset) (UKB data field 2966) 108,174 European ancestry individuals NA Affymetrix, Illumina [195080] 0 hypertension, age at onset http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90078976 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of tiredness or low energy - Nearly every day (UKB data field 20519) (Gene-based burden) 7,815 European ancestry cases, 131,607 European ancestry controls NA Illumina [172112] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082593 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Smokes on most or all days (UKB data field 22506) 2,527 European ancestry cases, 105,181 European ancestry controls NA Affymetrix, Illumina [194969] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078874 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of tiredness or low energy - Several days (UKB data field 20519) (Gene-based burden) 54,906 European ancestry cases, 84,516 European ancestry controls NA Illumina [172112] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082591 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Occasionally (UKB data field 22506) 1,697 European ancestry cases, 106,011 European ancestry controls NA Affymetrix, Illumina [194969] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078875 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings or nervousness or anxiety - More than half the days (UKB data field 20506) (Gene-based burden) 3,168 European ancestry cases, 135,994 European ancestry controls NA Illumina [172049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082549 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Ex smoker (UKB data field 22506) 39,575 European ancestry cases, 68,133 European ancestry controls NA Affymetrix, Illumina [194969] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078876 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings or nervousness or anxiety - Nearly every day (UKB data field 20506) (Gene-based burden) 3,224 European ancestry cases, 135,938 European ancestry controls NA Illumina [172049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082550 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Never smoked (UKB data field 22506) 63,909 European ancestry cases, 43,799 European ancestry controls NA Affymetrix, Illumina [194969] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078877 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings or nervousness or anxiety - Several days (UKB data field 20506) (Gene-based burden) 33,499 European ancestry cases, 105,663 European ancestry controls NA Illumina [172049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082548 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism angle left (UKB data field 5089) 107,117 European ancestry individuals NA Affymetrix, Illumina [194721] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90079272 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent inability to stop or control worrying - More than half the days (UKB data field 20509) (Gene-based burden) 3,165 European ancestry cases, 135,984 European ancestry controls NA Illumina [172050] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082558 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - Cylindrical power left (UKB data field 5086) 107,117 European ancestry individuals NA Affymetrix, Illumina [194721] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079269 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent inability to stop or control worrying - Nearly every day (UKB data field 20509) (Gene-based burden) 3,553 European ancestry cases, 135,596 European ancestry controls NA Illumina [172050] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082559 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical power left (UKB data field 5085) 107,117 European ancestry individuals NA Affymetrix, Illumina [194721] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079268 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent inability to stop or control worrying - Several days (UKB data field 20509) (Gene-based burden) 26,710 European ancestry cases, 112,439 European ancestry controls NA Illumina [172050] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082557 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent left 107,117 European ancestry individuals NA Affymetrix, Illumina [194721] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081510 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent lack of interest or pleasure in doing things - More than half the days (UKB data field 20514) (Gene-based burden) 3,128 European ancestry cases, 136,224 European ancestry controls NA Illumina [172101] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082576 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Abandoned (UKB data field 20246) 4,329 European ancestry cases, 102,771 European ancestry controls NA Affymetrix, Illumina [194222] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078385 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent lack of interest or pleasure in doing things - Nearly every day (UKB data field 20514) (Gene-based burden) 2,264 European ancestry cases, 137,088 European ancestry controls NA Illumina [172101] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082577 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Completed (UKB data field 20246) 92,699 European ancestry cases, 14,401 European ancestry controls NA Affymetrix, Illumina [194222] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078384 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent lack of interest or pleasure in doing things - Several days (UKB data field 20514) (Gene-based burden) 21,161 European ancestry cases, 118,191 European ancestry controls NA Illumina [172101] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082575 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Completed with pause (UKB data field 20246) 2,821 European ancestry cases, 104,279 European ancestry controls NA Affymetrix, Illumina [194222] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078386 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - paroxetine (Gene-based burden) 1,461 European ancestry cases, 319,297 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082028 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of lower-inner quadrant of breast (UKB data field 40006) 543 European ancestry cases, 40,462 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079103 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - perindopril (Gene-based burden) 6,331 European ancestry cases, 314,427 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082115 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of lower-outer quadrant of breast (UKB data field 40006) 636 European ancestry cases, 40,369 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079105 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - cousin (UKB data field 20173) 59,485 European ancestry cases, 47,354 European ancestry controls NA Affymetrix, Illumina [193767] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078343 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent thoughts of suicide or self harm - Not at all (UKB data field 20513) (Gene-based burden) 132,664 European ancestry cases, 5,980 European ancestry controls NA Illumina [171976] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082572 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - niece (UKB data field 20173) 12,210 European ancestry cases, 94,629 European ancestry controls NA Affymetrix, Illumina [193767] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078342 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent thoughts of suicide or self harm - Several days (UKB data field 20513) (Gene-based burden) 4,870 European ancestry cases, 133,774 European ancestry controls NA Illumina [171976] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082573 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - no relation (UKB data field 20173) 14,557 European ancestry cases, 92,282 European ancestry controls NA Affymetrix, Illumina [193767] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078344 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble concentrating on things - More than half the days (UKB data field 20508) (Gene-based burden) 2,878 European ancestry cases, 136,635 European ancestry controls NA Illumina [172111] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082555 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - sister (UKB data field 20173) 10,386 European ancestry cases, 96,453 European ancestry controls NA Affymetrix, Illumina [193767] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078341 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble concentrating on things - Nearly every day (UKB data field 20508) (Gene-based burden) 2,356 European ancestry cases, 137,157 European ancestry controls NA Illumina [172111] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082556 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever stopped smoking for 6 months (UKB data field 2907) 47,242 European ancestry cases, 60,216 European ancestry controls NA Affymetrix, Illumina [193687] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90078970 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble concentrating on things - Several days (UKB data field 20508) (Gene-based burden) 20,324 European ancestry cases, 119,189 European ancestry controls NA Illumina [172111] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082554 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal hysteresis right (UKB data field 5256) 105,888 European ancestry individuals NA Affymetrix, Illumina [192748] 0 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST90079335 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble relaxing - More than half the days (UKB data field 20515) (Gene-based burden) 4,031 European ancestry cases, 135,255 European ancestry controls NA Illumina [172094] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082579 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal resistance factor right (UKB data field 5257) 105,888 European ancestry individuals NA Affymetrix, Illumina [192748] 0 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST90079336 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble relaxing - Nearly every day (UKB data field 20515) (Gene-based burden) 4,293 European ancestry cases, 134,993 European ancestry controls NA Illumina [172094] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082580 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure corneal compensated right (UKB data field 5254) 105,888 European ancestry individuals 34,406 European ancestry individuals Affymetrix, Illumina [192748] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90079333 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble relaxing - Several days (UKB data field 20515) (Gene-based burden) 32,017 European ancestry cases, 107,269 European ancestry controls NA Illumina [172094] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082578 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraocular pressure Goldmann correlated right (UKB data field 5255) 105,888 European ancestry individuals 34,406 European ancestry individuals Affymetrix, Illumina [192748] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90079334 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent worrying too much about different things - More than half the days (UKB data field 20520) (Gene-based burden) 3,663 European ancestry cases, 135,464 European ancestry controls NA Illumina [172049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082595 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal hysteresis left (UKB data field 5264) 105,697 European ancestry individuals NA Affymetrix, Illumina [192579] 1 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST90079339 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent worrying too much about different things - Nearly every day (UKB data field 20520) (Gene-based burden) 3,952 European ancestry cases, 135,175 European ancestry controls NA Illumina [172049] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082596 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal resistance factor left (UKB data field 5265) 105,697 European ancestry individuals NA Affymetrix, Illumina [192579] 1 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST90079340 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent medication for asthma (UKB data field 22167) (Gene-based burden) 8,505 European ancestry cases, 5,230 European ancestry controls NA Illumina [90496] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082854 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Timed out due to inactivity (UKB data field 20246) 7,251 European ancestry cases, 99,849 European ancestry controls NA Affymetrix, Illumina [194222] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078387 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent medication for hayfever or allergic rhinitis (UKB data field 22166) (Gene-based burden) 11,761 European ancestry cases, 12,789 European ancestry controls NA Illumina [115200] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082853 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit completion status - Abandoned (UKB data field 20245) 2,095 European ancestry cases, 104,769 European ancestry controls NA Affymetrix, Illumina [193896] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078382 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent poor appetite or overeating - More than half the days (UKB data field 20511) (Gene-based burden) 3,964 European ancestry cases, 135,560 European ancestry controls NA Illumina [172115] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082567 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit completion status - Completed (UKB data field 20245) 102,495 European ancestry cases, 4,369 European ancestry controls NA Affymetrix, Illumina [193896] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078381 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent poor appetite or overeating - Nearly every day (UKB data field 20511) (Gene-based burden) 3,494 European ancestry cases, 136,030 European ancestry controls NA Illumina [172115] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082568 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit completion status - Completed with pause (UKB data field 20245) 2,274 European ancestry cases, 104,590 European ancestry controls NA Affymetrix, Illumina [193896] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078383 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent poor appetite or overeating - Several days (UKB data field 20511) (Gene-based burden) 18,394 European ancestry cases, 121,130 European ancestry controls NA Illumina [172115] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082566 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anisometropia 106,495 European ancestry individuals NA Affymetrix, Illumina [193793] 0 Anisometropia http://purl.obolibrary.org/obo/HP_0012803 GCST90081453 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent restlessness - More than half the days (UKB data field 20516) (Gene-based burden) 1,888 European ancestry cases, 137,492 European ancestry controls NA Illumina [172090] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082582 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean spherical equivalent 106,495 European ancestry individuals NA Affymetrix, Illumina [193793] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081497 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent restlessness - Nearly every day (UKB data field 20516) (Gene-based burden) 1,553 European ancestry cases, 137,827 European ancestry controls NA Illumina [172090] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082583 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Refractive astigmatism 106,495 European ancestry individuals NA Affymetrix, Illumina [193793] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90081506 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent restlessness - Several days (UKB data field 20516) (Gene-based burden) 13,527 European ancestry cases, 125,853 European ancestry controls NA Illumina [172090] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082581 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - aunt (UKB data field 20173) 10,201 European ancestry cases, 96,638 European ancestry controls NA Affymetrix, Illumina [193767] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078340 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent thoughts of suicide or self harm - More than half the days (UKB data field 20513) (Gene-based burden) 627 European ancestry cases, 138,017 European ancestry controls NA Illumina [171976] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082574 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - methotrexate (Gene-based burden) 2,438 European ancestry cases, 318,320 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082037 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Psychological over eating or binge eating (UKB data field 20544) 604 European ancestry cases, 43,660 European ancestry controls NA Affymetrix, Illumina [89212] 0 binge eating http://www.ebi.ac.uk/efo/EFO_0005924 GCST90078638 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - metoclopramide (Gene-based burden) 530 European ancestry cases, 320,228 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082073 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Agoraphobia (UKB data field 20544) 557 European ancestry cases, 43,707 European ancestry controls NA Affymetrix, Illumina [89212] 0 agoraphobia http://www.ebi.ac.uk/efo/EFO_1001872 GCST90078641 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - metoprolol (Gene-based burden) 841 European ancestry cases, 319,917 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082083 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Childhood asthma vs adult asthma 16,952 European ancestry cases, 26,201 European ancestry controls NA Affymetrix, Illumina [87728] 0 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90081472 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - microgynon (Gene-based burden) 633 European ancestry cases, 320,125 European ancestry controls NA Illumina [182834] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082035 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adult asthma 16,937 European ancestry cases, 26,201 European ancestry controls NA Affymetrix, Illumina [87689] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081448 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - micronor tablet (Gene-based burden) 612 European ancestry cases, 320,146 European ancestry controls NA Illumina [48204] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082036 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Professional informed about anxiety (UKB data field 20428) 26,395 European ancestry cases, 16,765 European ancestry controls NA Affymetrix, Illumina [87129] 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90078445 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - migraleve tablet (Gene-based burden) 588 European ancestry cases, 320,170 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082185 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Never (UKB data field 20539) 665 European ancestry cases, 42,373 European ancestry controls NA Affymetrix, Illumina [86961] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078627 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - minerals magnesium (Gene-based burden) 1,035 European ancestry cases, 319,723 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082160 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Often (UKB data field 20539) 18,096 European ancestry cases, 24,942 European ancestry controls NA Affymetrix, Illumina [86961] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078630 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mirena 24hrs intrauterine system (Gene-based burden) 674 European ancestry cases, 320,084 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082140 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Rarely (UKB data field 20539) 5,015 European ancestry cases, 38,023 European ancestry controls NA Affymetrix, Illumina [86961] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078628 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mirtazapine (Gene-based burden) 1,305 European ancestry cases, 319,453 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082169 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Sometimes (UKB data field 20539) 19,262 European ancestry cases, 23,776 European ancestry controls NA Affymetrix, Illumina [86961] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078629 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mometasone (Gene-based burden) 939 European ancestry cases, 319,819 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082108 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Never (UKB data field 20537) 608 European ancestry cases, 42,310 European ancestry controls NA Affymetrix, Illumina [86715] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078622 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - montelukast product (Gene-based burden) 897 European ancestry cases, 319,861 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082174 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Often (UKB data field 20537) 18,917 European ancestry cases, 24,001 European ancestry controls NA Affymetrix, Illumina [86715] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078625 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - movicol oral powder (Gene-based burden) 1,431 European ancestry cases, 319,327 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082151 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Rarely (UKB data field 20537) 4,438 European ancestry cases, 38,480 European ancestry controls NA Affymetrix, Illumina [86715] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078623 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - multivitamin mineral preparations (Gene-based burden) 6,375 European ancestry cases, 314,383 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082067 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Sometimes (UKB data field 20537) 18,955 European ancestry cases, 23,963 European ancestry controls NA Affymetrix, Illumina [86715] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078624 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - multivitamins (Gene-based burden) 14,139 European ancestry cases, 306,619 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081982 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequent trouble falling or staying asleep during worst period of anxiety (UKB data field 20427) 34,560 European ancestry cases, 7,692 European ancestry controls NA Affymetrix, Illumina [85441] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90078444 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - naproxen (Gene-based burden) 3,379 European ancestry cases, 317,379 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082051 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of things worried about during worst period of anxiety - More than one thing (UKB data field 20543) 23,769 European ancestry cases, 18,409 European ancestry controls NA Affymetrix, Illumina [85356] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078635 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nasonex aqueous nasal spray (Gene-based burden) 2,274 European ancestry cases, 318,484 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082167 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of things worried about during worst period of anxiety - One thing (UKB data field 20543) 18,409 European ancestry cases, 23,769 European ancestry controls NA Affymetrix, Illumina [85356] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078634 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nexium (Gene-based burden) 769 European ancestry cases, 319,989 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082197 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 6 (UKB data field 21036) 4,639 European ancestry cases, 40,302 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078738 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - indapamide (Gene-based burden) 1,602 European ancestry cases, 319,156 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082021 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 7 (UKB data field 21036) 4,551 European ancestry cases, 40,390 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078739 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - insulin product (Gene-based burden) 4,350 European ancestry cases, 316,408 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082092 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 8 (UKB data field 21036) 2,679 European ancestry cases, 42,262 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078740 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ipratropium (Gene-based burden) 552 European ancestry cases, 320,206 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082095 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 9 (UKB data field 21036) 792 European ancestry cases, 44,149 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078741 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - irbesartan (Gene-based burden) 3,196 European ancestry cases, 317,562 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082170 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture resulting from simple fall (UKB data field 3005) 26,807 European ancestry cases, 17,827 European ancestry controls NA Affymetrix, Illumina [90019] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90078984 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - iron product (Gene-based burden) 1,367 European ancestry cases, 319,391 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082111 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - No days with pain (UKB data field 21037) 3,561 European ancestry cases, 41,133 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078742 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - isosorbide mononitrate (Gene-based burden) 1,481 European ancestry cases, 319,277 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081987 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 1 day with pain (UKB data field 21037) 12,933 European ancestry cases, 31,761 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078744 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - kliovance (Gene-based burden) 929 European ancestry cases, 319,829 European ancestry controls NA Illumina [183908] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082184 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 10 days with pain (UKB data field 21037) 1,745 European ancestry cases, 42,949 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078743 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lacri lube eye ointment (Gene-based burden) 679 European ancestry cases, 320,079 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082086 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 2 days with pain (UKB data field 21037) 8,612 European ancestry cases, 36,082 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078745 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lactulose product (Gene-based burden) 1,198 European ancestry cases, 319,560 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082020 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 3 days with pain (UKB data field 21037) 5,411 European ancestry cases, 39,283 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078746 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lamotrigine (Gene-based burden) 573 European ancestry cases, 320,185 European ancestry controls NA Illumina [19152] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082055 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 4 days with pain (UKB data field 21037) 2,902 European ancestry cases, 41,792 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078747 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lansoprazole (Gene-based burden) 16,815 European ancestry cases, 303,943 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082011 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 5 days with pain (UKB data field 21037) 3,363 European ancestry cases, 41,331 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078748 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - latanoprost (Gene-based burden) 1,062 European ancestry cases, 319,696 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082162 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 6 days with pain (UKB data field 21037) 1,778 European ancestry cases, 42,916 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078749 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50: testicular problems (not cancer) (Gene-based burden) 518 European ancestry cases, 150,640 European ancestry controls NA Illumina [172888] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90081707 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent inability to stop or control worrying - Nearly every day (UKB data field 20509) 3,553 European ancestry cases, 135,596 European ancestry controls NA Affymetrix, Illumina [240581] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078573 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Thyroid problem (not cancer) (Gene-based burden) 1,214 European ancestry cases, 330,540 European ancestry controls NA Illumina [184201] 0 thyroid disease http://www.ebi.ac.uk/efo/EFO_1000627 GCST90081712 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent inability to stop or control worrying - Several days (UKB data field 20509) 26,710 European ancestry cases, 112,439 European ancestry controls NA Affymetrix, Illumina [240581] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078571 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E07: thyroid problem (not cancer) (Gene-based burden) 1,135 European ancestry cases, 327,917 European ancestry controls NA Illumina [184145] 0 thyroid disease http://www.ebi.ac.uk/efo/EFO_1000627 GCST90081713 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings or nervousness or anxiety - More than half the days (UKB data field 20506) 3,168 European ancestry cases, 135,994 European ancestry controls NA Affymetrix, Illumina [240558] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078563 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus tiniitis (Gene-based burden) 1,618 European ancestry cases, 330,136 European ancestry controls NA Illumina [184201] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90081939 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings or nervousness or anxiety - Nearly every day (UKB data field 20506) 3,224 European ancestry cases, 135,938 European ancestry controls NA Affymetrix, Illumina [240558] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078564 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93: tinnitus tiniitis (Gene-based burden) 1,297 European ancestry cases, 327,755 European ancestry controls NA Illumina [184145] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90081940 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings or nervousness or anxiety - Several days (UKB data field 20506) 33,499 European ancestry cases, 105,663 European ancestry controls NA Affymetrix, Illumina [240558] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078562 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tonsiltis (Gene-based burden) 5,112 European ancestry cases, 326,642 European ancestry controls NA Illumina [184201] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90081941 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diagnosed with life threatening illness - Never (UKB data field 20528) 116,449 European ancestry cases, 22,727 European ancestry controls NA Affymetrix, Illumina [240551] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078611 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J03: tonsiltis (Gene-based burden) 4,551 European ancestry cases, 324,501 European ancestry controls NA Illumina [184145] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90081942 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diagnosed with life threatening illness but not in the last 12 months (UKB data field 20528) 19,704 European ancestry cases, 119,472 European ancestry controls NA Affymetrix, Illumina [240551] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90078612 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Transient ischaemic attack tia (Gene-based burden) 1,877 European ancestry cases, 329,877 European ancestry controls NA Illumina [184201] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90081651 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diagnosed with life threatening illness within the last 12 months (UKB data field 20528) 3,023 European ancestry cases, 136,153 European ancestry controls NA Affymetrix, Illumina [240551] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90078613 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G45: transient ischaemic attack tia (Gene-based burden) 1,611 European ancestry cases, 327,441 European ancestry controls NA Illumina [184145] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90081652 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever contemplated self harm more than once (UKB data field 20485) 10,186 European ancestry cases, 128,964 European ancestry controls NA Affymetrix, Illumina [240548] 0 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST90078519 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trapped nerve compressed nerve (Gene-based burden) 1,550 European ancestry cases, 330,204 European ancestry controls NA Illumina [184201] 0 nerve compression syndrome http://www.ebi.ac.uk/efo/EFO_0009487 GCST90081723 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever contemplated self harm once (UKB data field 20485) 10,426 European ancestry cases, 128,724 European ancestry controls NA Affymetrix, Illumina [240548] 0 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST90078518 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55: trapped nerve compressed nerve (Gene-based burden) 1,460 European ancestry cases, 327,592 European ancestry controls NA Illumina [184145] 0 nerve compression syndrome http://www.ebi.ac.uk/efo/EFO_0009487 GCST90081724 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent worrying too much about different things - More than half the days (UKB data field 20520) 3,663 European ancestry cases, 135,464 European ancestry controls NA Affymetrix, Illumina [240531] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078609 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tuberculosis (Gene-based burden) 2,209 European ancestry cases, 329,545 European ancestry controls NA Illumina [184201] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90081832 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent worrying too much about different things - Nearly every day (UKB data field 20520) 3,952 European ancestry cases, 135,175 European ancestry controls NA Affymetrix, Illumina [240531] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078610 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A15: tuberculosis (Gene-based burden) 2,076 European ancestry cases, 326,976 European ancestry controls NA Illumina [184145] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90081833 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of upper-outer quadrant of breast (UKB data field 40006) (Gene-based burden) 3,434 European ancestry cases, 37,571 European ancestry controls NA Illumina [135851] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083090 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Started insulin within one year diabetes mellitis diagnosis (UKB data field 2986) 2,491 European ancestry cases, 18,545 European ancestry controls NA Affymetrix, Illumina [46424] 0 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90078977 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Melanoma in situ (UKB data field 40006) (Gene-based burden) 1,343 European ancestry cases, 72,887 European ancestry controls NA Illumina [155857] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083112 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Contemplated self harm in past year (UKB data field 20486) 4,107 European ancestry cases, 16,395 European ancestry controls NA Affymetrix, Illumina [44672] 0 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST90078520 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple myeloma (UKB data field 40006) (Gene-based burden) 554 European ancestry cases, 73,676 European ancestry controls NA Illumina [155857] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90083108 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - anxious (UKB data field 5779) 4,436 European ancestry cases, 15,928 European ancestry controls NA Affymetrix, Illumina [44671] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079378 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple myeloma and malignant plasma cell neoplasms (UKB data field 40006) (Gene-based burden) 609 European ancestry cases, 73,621 European ancestry controls NA Illumina [155857] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90083109 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - calm (UKB data field 5779) 717 European ancestry cases, 19,647 European ancestry controls NA Affymetrix, Illumina [44671] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079377 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neoplasm of uncertain behavior of bladder (UKB data field 40006) (Gene-based burden) 799 European ancestry cases, 73,431 European ancestry controls NA Illumina [155857] 0 bladder tumor http://www.ebi.ac.uk/efo/EFO_0000294 GCST90083121 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - tense (UKB data field 5779) 14,752 European ancestry cases, 5,612 European ancestry controls NA Affymetrix, Illumina [44671] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079380 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neoplasm of uncertain behavior of urinary organs (UKB data field 40006) (Gene-based burden) 842 European ancestry cases, 73,388 European ancestry controls NA Illumina [155857] 0 urinary system neoplasm http://purl.obolibrary.org/obo/MONDO_0021066 GCST90083122 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - worried (UKB data field 5779) 869 European ancestry cases, 19,495 European ancestry controls NA Affymetrix, Illumina [44671] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079379 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-follicular lymphoma (UKB data field 40006) (Gene-based burden) 965 European ancestry cases, 73,265 European ancestry controls NA Illumina [155857] 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90083106 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Discomfort pain occurring only during menstrual bleed (UKB data field 21026) 954 European ancestry cases, 19,437 European ancestry controls NA Affymetrix, Illumina [44279] 0 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90078695 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin (UKB data field 40006) (Gene-based burden) 21,805 European ancestry cases, 52,425 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083087 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 92 (UKB data field 20183) 571 European ancestry cases, 18,959 European ancestry controls NA Affymetrix, Illumina [42895] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078365 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of ear and external auricular canal (UKB data field 40006) (Gene-based burden) 667 European ancestry cases, 73,563 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083080 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 93 (UKB data field 20183) 1,095 European ancestry cases, 18,435 European ancestry controls NA Affymetrix, Illumina [42895] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078364 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of eyelid, including canthus (UKB data field 40006) (Gene-based burden) 887 European ancestry cases, 73,343 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083079 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 94 (UKB data field 20183) 917 European ancestry cases, 18,613 European ancestry controls NA Affymetrix, Illumina [42895] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078363 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of lower limb, including hip (UKB data field 40006) (Gene-based burden) 1,080 European ancestry cases, 73,150 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083085 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 95 (UKB data field 20183) 16,244 European ancestry cases, 3,286 European ancestry controls NA Affymetrix, Illumina [42895] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078362 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of parts of face (UKB data field 40006) (Gene-based burden) 5,918 European ancestry cases, 68,312 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083081 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 96 (UKB data field 20183) 703 European ancestry cases, 18,827 European ancestry controls NA Affymetrix, Illumina [42895] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078361 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of scalp and neck (UKB data field 40006) (Gene-based burden) 1,246 European ancestry cases, 72,984 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083082 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent worrying too much about different things - Several days (UKB data field 20520) 37,314 European ancestry cases, 101,813 European ancestry controls NA Affymetrix, Illumina [240531] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078608 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes (Gene-based burden) 3,497 European ancestry cases, 328,257 European ancestry controls NA Illumina [184201] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90081710 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of inadequacy - More than half the days (UKB data field 20507) 3,036 European ancestry cases, 136,011 European ancestry controls NA Affymetrix, Illumina [240424] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078566 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11: type 2 diabetes (Gene-based burden) 3,203 European ancestry cases, 325,849 European ancestry controls NA Illumina [184145] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90081711 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of inadequacy - Nearly every day (UKB data field 20507) 2,929 European ancestry cases, 136,118 European ancestry controls NA Affymetrix, Illumina [240424] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078567 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ulcerative colitis (Gene-based burden) 2,363 European ancestry cases, 329,391 European ancestry controls NA Illumina [184201] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90081857 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of inadequacy - Several days (UKB data field 20507) 21,459 European ancestry cases, 117,588 European ancestry controls NA Affymetrix, Illumina [240424] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078565 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K51: Ulcerative colitis (Gene-based burden) 2,210 European ancestry cases, 326,842 European ancestry controls NA Illumina [184145] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90081858 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever heard an unreal voice (UKB data field 20463) 2,438 European ancestry cases, 136,626 European ancestry controls NA Affymetrix, Illumina [240421] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078502 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Umbilical hernia (Gene-based burden) 521 European ancestry cases, 331,233 European ancestry controls NA Illumina [184201] 0 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90081897 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of foreboding - More than half the days (UKB data field 20512) 2,372 European ancestry cases, 136,661 European ancestry controls NA Affymetrix, Illumina [240385] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078584 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urinary frequency incontinence (Gene-based burden) 2,619 European ancestry cases, 329,135 European ancestry controls NA Illumina [184201] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90081702 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of foreboding - Nearly every day (UKB data field 20512) 2,447 European ancestry cases, 136,586 European ancestry controls NA Affymetrix, Illumina [240385] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078585 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R15: urinary frequency incontinence (Gene-based burden) 2,477 European ancestry cases, 326,575 European ancestry controls NA Illumina [184145] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90081703 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of foreboding - Several days (UKB data field 20512) 18,747 European ancestry cases, 120,286 European ancestry controls NA Affymetrix, Illumina [240385] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078583 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urinary tract infection or kidney infection (Gene-based burden) 2,380 European ancestry cases, 329,374 European ancestry controls NA Illumina [184201] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90081696 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent easy annoyance or irritability - More than half the days (UKB data field 20505) 2,811 European ancestry cases, 136,216 European ancestry controls NA Affymetrix, Illumina [240379] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90078560 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N390: Urinary tract infection or kidney infection (Gene-based burden) 2,144 European ancestry cases, 326,908 European ancestry controls NA Illumina [184145] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90081697 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent easy annoyance or irritability - Nearly every day (UKB data field 20505) 2,044 European ancestry cases, 136,983 European ancestry controls NA Affymetrix, Illumina [240379] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90078561 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Uterine fibroids (Gene-based burden) 7,143 European ancestry cases, 324,611 European ancestry controls NA Illumina [184201] 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90081782 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent easy annoyance or irritability - Several days (UKB data field 20505) 33,713 European ancestry cases, 105,314 European ancestry controls NA Affymetrix, Illumina [240379] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90078559 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25: uterine fibroids (Gene-based burden) 6,313 European ancestry cases, 171,581 European ancestry controls NA Illumina [177166] 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90081783 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at menopause - last menstrual period (UKB data field 3581) 140,172 European ancestry individuals NA Affymetrix, Illumina [240319] 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90079064 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Uterine polyps (Gene-based burden) 1,439 European ancestry cases, 330,315 European ancestry controls NA Illumina [184201] 0 uterine polyp http://www.ebi.ac.uk/efo/EFO_0009484 GCST90081784 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Extremely happy (UKB data field 20458) 13,968 European ancestry cases, 124,983 European ancestry controls NA Affymetrix, Illumina [240215] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078481 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I46.0: Cardiac arrest with successful resuscitation 895 European ancestry cases, 387,035 European ancestry controls NA Affymetrix, Illumina [237612] 0 GCST90080008 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 2 days with pain (UKB data field 21037) (Gene-based burden) 8,612 European ancestry cases, 36,082 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082731 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 predicted (UKB data field 20153) 136,823 European ancestry individuals 25,462 European ancestry individuals Affymetrix, Illumina [237405] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90078319 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 3 days with pain (UKB data field 21037) (Gene-based burden) 5,411 European ancestry cases, 39,283 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082732 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 predicted percentage (UKB data field 20154) 136,823 European ancestry individuals NA Affymetrix, Illumina [237405] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90078320 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 4 days with pain (UKB data field 21037) (Gene-based burden) 2,902 European ancestry cases, 41,792 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082733 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 68 (UKB data field 4990) 723 European ancestry cases, 135,668 European ancestry controls NA Affymetrix, Illumina [236885] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079248 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 5 days with pain (UKB data field 21037) (Gene-based burden) 3,363 European ancestry cases, 41,331 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082734 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 69 (UKB data field 4990) 106,949 European ancestry cases, 29,442 European ancestry controls NA Affymetrix, Illumina [236885] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079249 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 6 days with pain (UKB data field 21037) (Gene-based burden) 1,778 European ancestry cases, 42,916 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082735 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of cecum (UKB data field 40006) (Gene-based burden) 648 European ancestry cases, 73,582 European ancestry controls NA Illumina [155857] 0 cecal neoplasm http://www.ebi.ac.uk/efo/EFO_0009255 GCST90083066 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 6 (UKB data field 6332) 14,457 European ancestry cases, 9,982 European ancestry controls NA Affymetrix, Illumina [53263] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079500 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of colon (UKB data field 40006) (Gene-based burden) 3,309 European ancestry cases, 70,921 European ancestry controls NA Illumina [155857] 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90083068 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 7 (UKB data field 6332) 20,635 European ancestry cases, 3,804 European ancestry controls NA Affymetrix, Illumina [53263] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079501 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of corpus uteri (UKB data field 40006) (Gene-based burden) 1,612 European ancestry cases, 39,393 European ancestry controls NA Illumina [135851] 0 uterine corpus cancer http://www.ebi.ac.uk/efo/EFO_0007532 GCST90083096 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - top left (UKB data field 6332) 23,512 European ancestry cases, 927 European ancestry controls NA Affymetrix, Illumina [53263] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079496 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of endometrium (UKB data field 40006) (Gene-based burden) 1,536 European ancestry cases, 39,469 European ancestry controls NA Illumina [135851] 0 endometrial cancer http://purl.obolibrary.org/obo/MONDO_0011962 GCST90083095 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C43.7: Malignant melanoma of lower limb, including hip 793 European ancestry cases, 387,137 European ancestry controls NA Affymetrix, Illumina [52952] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079592 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of esophagus (UKB data field 40006) (Gene-based burden) 696 European ancestry cases, 73,534 European ancestry controls NA Illumina [155857] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90083065 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K70.9: Alcoholic liver disease, unspecified 709 European ancestry cases, 387,221 European ancestry controls NA Affymetrix, Illumina [52952] 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90080282 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of kidney, except renal pelvis (UKB data field 40006) (Gene-based burden) 1,214 European ancestry cases, 73,016 European ancestry controls NA Illumina [155857] 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90083100 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z40.0: Encounter for prophylactic surgery for risk factors related to malignant neoplasms 796 European ancestry cases, 387,134 European ancestry controls NA Affymetrix, Illumina [52952] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081253 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of lower lobe, bronchus or lung (UKB data field 40006) (Gene-based burden) 626 European ancestry cases, 73,604 European ancestry controls NA Illumina [155857] 0 lung neoplasm http://purl.obolibrary.org/obo/MONDO_0021117 GCST90083072 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M07: Enteropathic arthropathies 906 European ancestry cases, 387,013 European ancestry controls NA Affymetrix, Illumina [52950] 0 Arthropathy http://purl.obolibrary.org/obo/HP_0003040 GCST90080393 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of lower-inner quadrant of breast (UKB data field 40006) (Gene-based burden) 543 European ancestry cases, 40,462 European ancestry controls NA Illumina [135851] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083089 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.4: Multiple fractures of ribs 1,087 European ancestry cases, 386,549 European ancestry controls NA Affymetrix, Illumina [52921] 0 multiple bone fractures http://www.ebi.ac.uk/efo/EFO_0009513 GCST90080962 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of lower-outer quadrant of breast (UKB data field 40006) (Gene-based burden) 636 European ancestry cases, 40,369 European ancestry controls NA Illumina [135851] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083091 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 3 moves (UKB data field 6312) 23,387 European ancestry cases, 862 European ancestry controls NA Affymetrix, Illumina [52881] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079492 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of ovary (UKB data field 40006) (Gene-based burden) 1,106 European ancestry cases, 39,899 European ancestry controls NA Illumina [135851] 0 ovarian neoplasm http://www.ebi.ac.uk/efo/EFO_0003893 GCST90083097 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 4 moves (UKB data field 6312) 21,604 European ancestry cases, 2,645 European ancestry controls NA Affymetrix, Illumina [52881] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079493 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of overlapping sites of breast (UKB data field 40006) (Gene-based burden) 878 European ancestry cases, 40,127 European ancestry controls NA Illumina [135851] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083092 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 5 moves (UKB data field 6312) 17,778 European ancestry cases, 6,471 European ancestry controls NA Affymetrix, Illumina [52881] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079494 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of pancreas (UKB data field 40006) (Gene-based burden) 682 European ancestry cases, 73,548 European ancestry controls NA Illumina [155857] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90083070 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 6 moves (UKB data field 6312) 5,999 European ancestry cases, 18,250 European ancestry controls NA Affymetrix, Illumina [52881] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079495 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of prostate (UKB data field 40006) (Gene-based burden) 8,498 European ancestry cases, 24,727 European ancestry controls NA Illumina [126421] 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90083098 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent medication for hayfever or allergic rhinitis (UKB data field 22166) 11,761 European ancestry cases, 12,789 European ancestry controls NA Affymetrix, Illumina [52460] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078867 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of rectum (UKB data field 40006) (Gene-based burden) 1,566 European ancestry cases, 72,664 European ancestry controls NA Illumina [155857] 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90083069 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for anxiety - Drugs or alcohol more than once (UKB data field 20549) 7,444 European ancestry cases, 16,129 European ancestry controls NA Affymetrix, Illumina [50569] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078662 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of sigmoid colon (UKB data field 40006) (Gene-based burden) 1,290 European ancestry cases, 72,940 European ancestry controls NA Illumina [155857] 0 sigmoid neoplasm http://www.ebi.ac.uk/efo/EFO_1001181 GCST90083067 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for anxiety - Medication prescribed to you for at least two weeks (UKB data field 20549) 17,819 European ancestry cases, 5,754 European ancestry controls NA Affymetrix, Illumina [50569] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078661 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of testis (UKB data field 40006) (Gene-based burden) 512 European ancestry cases, 32,713 European ancestry controls NA Illumina [126421] 0 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST90083099 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for anxiety - Unprescribed medication more than once (UKB data field 20549) 3,611 European ancestry cases, 19,962 European ancestry controls NA Affymetrix, Illumina [50569] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078660 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of thyroid gland (UKB data field 40006) (Gene-based burden) 546 European ancestry cases, 73,684 European ancestry controls NA Illumina [155857] 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90083104 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when walking ever disappears while walking (UKB data field 5496) 7,982 European ancestry cases, 13,580 European ancestry controls NA Affymetrix, Illumina [47079] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079354 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of unspecified part of bronchus or lung (UKB data field 40006) (Gene-based burden) 558 European ancestry cases, 73,672 European ancestry controls NA Illumina [155857] 0 lung neoplasm http://purl.obolibrary.org/obo/MONDO_0021117 GCST90083073 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat anxiety - Other therapeutic activities such as mindfulness yoga or art classes (UKB data field 20550) 7,965 European ancestry cases, 13,491 European ancestry controls NA Affymetrix, Illumina [46648] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90078664 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of upper lobe, bronchus or lung (UKB data field 40006) (Gene-based burden) 1,142 European ancestry cases, 73,088 European ancestry controls NA Illumina [155857] 0 lung neoplasm http://purl.obolibrary.org/obo/MONDO_0021117 GCST90083071 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat anxiety - Talking therapies such as psychotherapy counselling group therapy or CBT (UKB data field 20550) 17,885 European ancestry cases, 3,571 European ancestry controls NA Affymetrix, Illumina [46648] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90078663 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of upper-inner quadrant of breast (UKB data field 40006) (Gene-based burden) 1,025 European ancestry cases, 39,980 European ancestry controls NA Illumina [135851] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083088 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lamotrigine 573 European ancestry cases, 320,185 European ancestry controls NA Affymetrix, Illumina [46479] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078069 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vomiting when IBS symptoms first began (UKB data field 21076) 1,251 European ancestry cases, 17,399 European ancestry controls NA Affymetrix, Illumina [41361] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90078839 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of trunk (UKB data field 40006) (Gene-based burden) 2,568 European ancestry cases, 71,662 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083083 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Infectious illness diagnosis status when IBS symptoms first began (UKB data field 21071) 1,871 European ancestry cases, 16,625 European ancestry controls NA Affymetrix, Illumina [41113] 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90078835 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of upper limb, including shoulder (UKB data field 40006) (Gene-based burden) 1,381 European ancestry cases, 72,849 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083084 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diarrhoea when IBS symptoms first began (UKB data field 21074) 9,581 European ancestry cases, 8,922 European ancestry controls NA Affymetrix, Illumina [41085] 0 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST90078837 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin, unspecified (UKB data field 40006) (Gene-based burden) 8,504 European ancestry cases, 65,726 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083086 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fever when IBS symptoms first began (UKB data field 21073) 1,303 European ancestry cases, 17,177 European ancestry controls NA Affymetrix, Illumina [41036] 0 Fever http://purl.obolibrary.org/obo/HP_0001945 GCST90078836 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-Hodgkin lymphoma (UKB data field 40006) (Gene-based burden) 504 European ancestry cases, 73,726 European ancestry controls NA Illumina [155857] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90083107 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism - both eyes (UKB data field 5855) 12,485 European ancestry cases, 5,160 European ancestry controls NA Affymetrix, Illumina [39451] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90079393 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type of tobacco previously smoked - Cigars or pipes (UKB data field 2877) (Gene-based burden) 5,039 European ancestry cases, 103,837 European ancestry controls NA Illumina [166625] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082954 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism - left eye (UKB data field 5855) 2,864 European ancestry cases, 14,781 European ancestry controls NA Affymetrix, Illumina [39451] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90079392 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type of tobacco previously smoked - Hand rolled cigarettes (UKB data field 2877) (Gene-based burden) 7,435 European ancestry cases, 101,441 European ancestry controls NA Illumina [166625] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082953 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism - right eye (UKB data field 5855) 2,590 European ancestry cases, 15,055 European ancestry controls NA Affymetrix, Illumina [39451] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90079391 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type of tobacco previously smoked - Manufactured cigarettes (UKB data field 2877) (Gene-based burden) 96,924 European ancestry cases, 11,952 European ancestry controls NA Illumina [166625] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082952 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of onset of IBS symptoms - 801 Started suddenly (UKB data field 21070) 4,336 European ancestry cases, 9,842 European ancestry controls NA Affymetrix, Illumina [32630] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90078833 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urate levels (UKB data field 30880) (Gene-based burden) 411,604 European ancestry individuals NA Illumina [185661] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90083031 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of onset of IBS symptoms - 802 Came on gradually (UKB data field 21070) 9,842 European ancestry cases, 4,336 European ancestry controls NA Affymetrix, Illumina [32630] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90078834 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urea levels (UKB data field 30670) (Gene-based burden) 411,808 European ancestry individuals NA Illumina [185663] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90083008 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent medication for asthma (UKB data field 22167) 8,505 European ancestry cases, 5,230 European ancestry controls NA Affymetrix, Illumina [31694] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078868 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urinary albumin-to-creatinine ratio (Gene-based burden) 126,399 European ancestry individuals NA Illumina [170756] 0 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST90085519 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract - both eyes (UKB data field 5441) 6,814 European ancestry cases, 3,778 European ancestry controls NA Affymetrix, Illumina [26001] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079349 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Always (UKB data field 2267) (Gene-based burden) 96,475 European ancestry cases, 333,934 European ancestry controls NA Illumina [185924] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90082868 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract - left eye (UKB data field 5441) 1,817 European ancestry cases, 8,775 European ancestry controls NA Affymetrix, Illumina [26001] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079348 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Do not go out in sunshine (UKB data field 2267) (Gene-based burden) 2,503 European ancestry cases, 427,906 European ancestry controls NA Illumina [185924] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90082869 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract - right eye (UKB data field 5441) 2,144 European ancestry cases, 8,448 European ancestry controls NA Affymetrix, Illumina [26001] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079347 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84: uterine polyps (Gene-based burden) 1,299 European ancestry cases, 176,595 European ancestry controls NA Illumina [177166] 0 uterine polyp http://www.ebi.ac.uk/efo/EFO_0009484 GCST90081785 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Moderately happy (UKB data field 20458) 55,476 European ancestry cases, 83,475 European ancestry controls NA Affymetrix, Illumina [240215] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078483 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vaginal prolapse uterine prolapse (Gene-based burden) 2,758 European ancestry cases, 328,996 European ancestry controls NA Illumina [184201] 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90081786 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Moderately unhappy (UKB data field 20458) 6,122 European ancestry cases, 132,829 European ancestry controls NA Affymetrix, Illumina [240215] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078484 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N814: vaginal prolapse uterine prolapse (Gene-based burden) 2,633 European ancestry cases, 175,261 European ancestry controls NA Illumina [177166] 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90081787 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Very happy (UKB data field 20458) 61,849 European ancestry cases, 77,102 European ancestry controls NA Affymetrix, Illumina [240215] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078482 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Varicose veins (Gene-based burden) 2,152 European ancestry cases, 329,602 European ancestry controls NA Illumina [184201] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90081885 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Very unhappy (UKB data field 20458) 1,178 European ancestry cases, 137,773 European ancestry controls NA Affymetrix, Illumina [240215] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078485 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83: varicose veins (Gene-based burden) 1,821 European ancestry cases, 327,231 European ancestry controls NA Illumina [184145] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90081886 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever thought that life not worth living more than once (UKB data field 20479) 24,195 European ancestry cases, 114,587 European ancestry controls NA Affymetrix, Illumina [239990] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078511 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vertigo (Gene-based burden) 818 European ancestry cases, 330,936 European ancestry controls NA Illumina [184201] 0 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90081887 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever thought that life not worth living once (UKB data field 20479) 19,030 European ancestry cases, 119,752 European ancestry controls NA Affymetrix, Illumina [239990] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078510 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R42: vertigo (Gene-based burden) 673 European ancestry cases, 328,379 European ancestry controls NA Illumina [184145] 0 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90081888 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent thoughts of suicide or self harm - More than half the days (UKB data field 20513) 627 European ancestry cases, 138,017 European ancestry controls NA Affymetrix, Illumina [239840] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078588 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whooping cough pertussis (Gene-based burden) 1,336 European ancestry cases, 330,418 European ancestry controls NA Illumina [184201] 0 whooping cough http://www.ebi.ac.uk/efo/EFO_0000650 GCST90081935 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent thoughts of suicide or self harm - Not at all (UKB data field 20513) 132,664 European ancestry cases, 5,980 European ancestry controls NA Affymetrix, Illumina [239840] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078586 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A37: whooping cough pertussis (Gene-based burden) 1,179 European ancestry cases, 327,873 European ancestry controls NA Illumina [184145] 0 whooping cough http://www.ebi.ac.uk/efo/EFO_0000650 GCST90081936 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent thoughts of suicide or self harm - Several days (UKB data field 20513) 4,870 European ancestry cases, 133,774 European ancestry controls NA Affymetrix, Illumina [239840] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078587 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non cancer illness - year age first occurred (UKB data field 87) (Gene-based burden) 327,660 European ancestry individuals NA Illumina [184106] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90083490 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever seen an unreal vision (UKB data field 20471) 4,462 European ancestry cases, 133,755 European ancestry controls NA Affymetrix, Illumina [239255] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078507 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - No days with pain (UKB data field 21037) (Gene-based burden) 3,561 European ancestry cases, 41,133 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082728 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to any substance or behaviour (UKB data field 20401) 8,298 European ancestry cases, 129,860 European ancestry controls NA Affymetrix, Illumina [239059] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90078396 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 1 day with pain (UKB data field 21037) (Gene-based burden) 12,933 European ancestry cases, 31,761 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082730 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever suffered mental distress preventing usual activities (UKB data field 20500) 46,079 European ancestry cases, 91,780 European ancestry controls NA Affymetrix, Illumina [238689] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90078555 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 10 days with pain (UKB data field 21037) (Gene-based burden) 1,745 European ancestry cases, 42,949 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082729 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Most of the time (UKB data field 2267) (Gene-based burden) 166,473 European ancestry cases, 263,936 European ancestry controls NA Illumina [185924] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90082867 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood pressure medication use (UKB data field 6153) 42,217 European ancestry cases, 33,337 European ancestry controls NA Affymetrix, Illumina [25362] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079458 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Never rarely (UKB data field 2267) (Gene-based burden) 38,347 European ancestry cases, 392,062 European ancestry controls NA Illumina [185924] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90082865 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bloody diarrhoea when IBS symptoms first began (UKB data field 21075) 1,061 European ancestry cases, 8,491 European ancestry controls NA Affymetrix, Illumina [23597] 0 Hematochezia http://purl.obolibrary.org/obo/HP_0002573 GCST90078838 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Sometimes (UKB data field 2267) (Gene-based burden) 150,448 European ancestry cases, 279,961 European ancestry controls NA Illumina [185924] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90082866 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - anxious (UKB data field 20185) 1,927 European ancestry cases, 7,137 European ancestry controls NA Affymetrix, Illumina [22824] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078366 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Usual walking pace - Brisk pace (UKB data field 924) (Gene-based burden) 176,054 European ancestry cases, 252,201 European ancestry controls NA Illumina [185912] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083497 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - tense (UKB data field 20185) 6,747 European ancestry cases, 2,317 European ancestry controls NA Affymetrix, Illumina [22824] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078367 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Usual walking pace - Slow pace (UKB data field 924) (Gene-based burden) 34,629 European ancestry cases, 393,626 European ancestry controls NA Illumina [185912] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083495 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had cataract surgery - Both eyes (UKB data field 5324) 1,531 European ancestry cases, 7,169 European ancestry controls NA Affymetrix, Illumina [22363] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90079342 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Usual walking pace - Steady average pace (UKB data field 924) (Gene-based burden) 231,500 European ancestry cases, 196,755 European ancestry controls NA Illumina [185912] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083496 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had cataract surgery - Right eye only (UKB data field 5324) 588 European ancestry cases, 8,112 European ancestry controls NA Affymetrix, Illumina [22363] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90079341 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 3 moves (UKB data field 6312) (Gene-based burden) 23,387 European ancestry cases, 862 European ancestry controls NA Illumina [113125] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083478 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had laser eye surgery - Both eyes (UKB data field 5325) 1,848 European ancestry cases, 6,743 European ancestry controls NA Affymetrix, Illumina [22141] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90079343 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 4 moves (UKB data field 6312) (Gene-based burden) 21,604 European ancestry cases, 2,645 European ancestry controls NA Illumina [113125] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083479 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Chlamydia trachomatis (UKB data field 23070) 1,732 European ancestry cases, 6,809 European ancestry controls NA Affymetrix, Illumina [21784] 0 Chlamydia trachomatis seropositivity http://www.ebi.ac.uk/efo/EFO_0009330 GCST90078899 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 5 moves (UKB data field 6312) (Gene-based burden) 17,778 European ancestry cases, 6,471 European ancestry controls NA Illumina [113125] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083480 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Human Cytomegalovirus (UKB data field 23054) 4,835 European ancestry cases, 3,706 European ancestry controls NA Affymetrix, Illumina [21784] 0 cytomegalovirus seropositivity http://www.ebi.ac.uk/efo/EFO_0007037 GCST90078889 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tower rearranging - Value entered - 6 moves (UKB data field 6312) (Gene-based burden) 5,999 European ancestry cases, 18,250 European ancestry controls NA Illumina [113125] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083481 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Helicobacter pylori - definition 2 (UKB data field 23074) 2,568 European ancestry cases, 5,973 European ancestry controls NA Affymetrix, Illumina [21784] 0 Helicobacter pylori seropositivity http://www.ebi.ac.uk/efo/EFO_0009341 GCST90078901 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit substitution - Values entered (UKB data field 20229) (Gene-based burden) 105,636 European ancestry individuals NA Illumina [165850] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082359 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. HHV 6 overall seropositivity for Human Herpesvirus 6 (UKB data field 23055) 7,769 European ancestry cases, 772 European ancestry controls NA Affymetrix, Illumina [21784] 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90078890 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Verbal interview duration (UKB data field 3) (Gene-based burden) 430,929 European ancestry individuals NA Illumina [185950] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90083064 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. HHV 6A seropositivity for Human Herpesvirus 6 (UKB data field 23056) 6,648 European ancestry cases, 1,893 European ancestry controls NA Affymetrix, Illumina [21784] 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90078891 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Folic acid or Folate Vit B9 (UKB data field 6155) (Gene-based burden) 10,077 European ancestry cases, 132,748 European ancestry controls NA Illumina [173046] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90083456 Exome-wide sequencing 2021-08-31 33841421 Li J 2021-03-25 Front Immunol www.ncbi.nlm.nih.gov/pubmed/33841421 Variants at the MHC Region Associate With Susceptibility to Clostridioides difficile Infection: A Genome-Wide Association Study Using Comprehensive Electronic Health Records. Clostridioides difficle infection 1,160 European ancestry cases, 14,144 European ancestry controls NA Illumina [64973696] (imputed) 26 clostridium difficile infection http://www.ebi.ac.uk/efo/EFO_0009130 GCST012277 Genome-wide genotyping array 2021-08-31 33841421 Li J 2021-03-25 Front Immunol www.ncbi.nlm.nih.gov/pubmed/33841421 Variants at the MHC Region Associate With Susceptibility to Clostridioides difficile Infection: A Genome-Wide Association Study Using Comprehensive Electronic Health Records. Clostridioides difficle infection in antibiotics-users 587 European ancestry cases, 3,166 European ancestry controls NA Illumina [64973696] (imputed) 22 clostridium difficile infection http://www.ebi.ac.uk/efo/EFO_0009130 GCST012276 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.3: Ulcer of intestine 930 European ancestry cases, 386,975 European ancestry controls NA Affymetrix, Illumina [510666] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080270 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.8: Other specified bacterial agents as the cause of diseases classified elsewhere (Gene-based burden) 6,173 European ancestry cases, 380,226 European ancestry controls NA Illumina [185323] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083554 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M41.9: Scoliosis, unspecified 1,360 European ancestry cases, 386,551 European ancestry controls NA Affymetrix, Illumina [510666] 0 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST90080471 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B97: Viral agents as the cause of diseases classified elsewhere (Gene-based burden) 684 European ancestry cases, 387,059 European ancestry controls NA Illumina [185340] 0 viral disease http://www.ebi.ac.uk/efo/EFO_0000763 GCST90083556 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W22: Striking against or struck by other objects 959 European ancestry cases, 386,954 European ancestry controls NA Affymetrix, Illumina [510666] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081121 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B98: Other specified infectious agents as the cause of diseases classified to other chapters (Gene-based burden) 1,560 European ancestry cases, 386,369 European ancestry controls NA Illumina [185344] 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90083558 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C16: Malignant neoplasm of stomach 762 European ancestry cases, 387,139 European ancestry controls NA Affymetrix, Illumina [510665] 0 stomach neoplasm http://www.ebi.ac.uk/efo/EFO_0003897 GCST90079576 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B98.0: Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters (Gene-based burden) 1,559 European ancestry cases, 386,371 European ancestry controls NA Illumina [185344] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083557 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C22: Malignant neoplasm of liver and intrahepatic bile ducts 575 European ancestry cases, 387,333 European ancestry controls NA Affymetrix, Illumina [510665] 0 liver neoplasm http://www.ebi.ac.uk/efo/EFO_1001513 GCST90079584 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C15: Malignant neoplasm of esophagus (Gene-based burden) 992 European ancestry cases, 386,907 European ancestry controls NA Illumina [185344] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90083561 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C90.0: Multiple myeloma 739 European ancestry cases, 387,155 European ancestry controls NA Affymetrix, Illumina [510665] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90079639 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C15.5: Malignant neoplasm of lower third of esophagus (Gene-based burden) 556 European ancestry cases, 387,374 European ancestry controls NA Illumina [185344] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90083559 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V18: Pedal cycle rider injured in noncollision transport accident 1,465 European ancestry cases, 386,440 European ancestry controls NA Affymetrix, Illumina [510665] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081094 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C15.9: Malignant neoplasm of esophagus, unspecified (Gene-based burden) 864 European ancestry cases, 387,066 European ancestry controls NA Illumina [185344] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90083560 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.0: Presence of urogenital implants 2,038 European ancestry cases, 385,858 European ancestry controls NA Affymetrix, Illumina [510665] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081426 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C16: Malignant neoplasm of stomach (Gene-based burden) 762 European ancestry cases, 387,139 European ancestry controls NA Illumina [185344] 0 stomach neoplasm http://www.ebi.ac.uk/efo/EFO_0003897 GCST90083562 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I85: Esophageal varices 684 European ancestry cases, 387,221 European ancestry controls NA Affymetrix, Illumina [510664] 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90080076 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18: Malignant neoplasm of colon (Gene-based burden) 3,899 European ancestry cases, 383,758 European ancestry controls NA Illumina [185335] 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90083567 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I95.1: Orthostatic hypotension 2,084 European ancestry cases, 385,821 European ancestry controls NA Affymetrix, Illumina [510664] 0 orthostatic hypotension http://www.ebi.ac.uk/efo/EFO_0005252 GCST90080081 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.0: Malignant neoplasm of cecum (Gene-based burden) 774 European ancestry cases, 387,155 European ancestry controls NA Illumina [185344] 0 cecum cancer http://purl.obolibrary.org/obo/MONDO_0002033 GCST90083563 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J96: Respiratory failure, not elsewhere classified 3,157 European ancestry cases, 384,744 European ancestry controls NA Affymetrix, Illumina [510664] 0 respiratory failure http://www.ebi.ac.uk/efo/EFO_0009686 GCST90080157 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.2: Malignant neoplasm of ascending colon (Gene-based burden) 549 European ancestry cases, 387,381 European ancestry controls NA Illumina [185344] 0 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90083564 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T42.4: Poisoning by, adverse effect of and underdosing of benzodiazepines 643 European ancestry cases, 387,246 European ancestry controls NA Affymetrix, Illumina [510664] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081053 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.7: Malignant neoplasm of sigmoid colon (Gene-based burden) 1,470 European ancestry cases, 386,460 European ancestry controls NA Illumina [185344] 0 sigmoid neoplasm http://www.ebi.ac.uk/efo/EFO_1001181 GCST90083565 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y45: Adverse effects in the therapeutic use of analgesics, antipyretics and anti-inflammatory drugs 1,339 European ancestry cases, 386,562 European ancestry controls NA Affymetrix, Illumina [510664] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90081153 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08: Encounter for follow-up examination after completed treatment for malignant neoplasm 6,079 European ancestry cases, 381,838 European ancestry controls 443 European ancestry cases, 29,305 European ancestry controls Affymetrix, Illumina [510674] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081200 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inflammatory bowel disease - strict composite (Gene-based burden) 5,509 European ancestry cases, 321,797 European ancestry controls NA Illumina [184140] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90085475 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C71: Malignant neoplasm of brain 678 European ancestry cases, 387,224 European ancestry controls NA Affymetrix, Illumina [510673] 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90079614 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ulcerative colitis (Gene-based burden) 3,928 European ancestry cases, 321,797 European ancestry controls NA Illumina [184092] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90085476 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D18.0: Hemangioma 1,813 European ancestry cases, 386,087 European ancestry controls NA Affymetrix, Illumina [510673] 0 hemangioma http://www.ebi.ac.uk/efo/EFO_1000635 GCST90079670 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A04: Other bacterial intestinal infections (Gene-based burden) 3,566 European ancestry cases, 381,664 European ancestry controls NA Illumina [185294] 0 intestinal disease, bacterial disease http://www.ebi.ac.uk/efo/EFO_0009431, http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083525 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I12: Hypertensive chronic kidney disease 1,660 European ancestry cases, 386,252 European ancestry controls 7,955 European ancestry cases, 107,322 European ancestry controls Affymetrix, Illumina [510673] 0 hypertensive nephropathy http://purl.obolibrary.org/obo/MONDO_0024633 GCST90079964 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A04.7: Enterocolitis due to Clostridium difficile (Gene-based burden) 881 European ancestry cases, 387,046 European ancestry controls NA Illumina [185344] 0 clostridium difficile infection http://www.ebi.ac.uk/efo/EFO_0009130 GCST90083523 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S66.3: Injury of extensor muscle, fascia and tendon of other and unspecified finger at wrist and hand level 531 European ancestry cases, 387,384 European ancestry controls NA Affymetrix, Illumina [510673] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081005 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A04.8: Other specified bacterial intestinal infections (Gene-based burden) 1,799 European ancestry cases, 386,131 European ancestry controls NA Illumina [185344] 0 intestinal infectious disease http://purl.obolibrary.org/obo/MONDO_0000916 GCST90083524 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.0: Personal history of malignant neoplasm of digestive organs 6,500 European ancestry cases, 381,416 European ancestry controls 1,427 European ancestry cases, 33,898 European ancestry controls Affymetrix, Illumina [510673] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90081347 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A08: Viral and other specified intestinal infections (Gene-based burden) 1,306 European ancestry cases, 383,755 European ancestry controls NA Illumina [185297] 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90083527 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C25: Malignant neoplasm of pancreas 961 European ancestry cases, 386,943 European ancestry controls NA Affymetrix, Illumina [510672] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90079586 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A08.4: Viral intestinal infection, unspecified (Gene-based burden) 910 European ancestry cases, 387,020 European ancestry controls NA Illumina [185344] 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90083526 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.0: Entropion and trichiasis of eyelid 838 European ancestry cases, 387,070 European ancestry controls NA Affymetrix, Illumina [510672] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90079868 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A09: Infectious gastroenteritis and colitis, unspecified (Gene-based burden) 9,743 European ancestry cases, 374,480 European ancestry controls NA Illumina [185283] 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90083529 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z48.0: Encounter for attention to dressings, sutures and drains 564 European ancestry cases, 387,356 European ancestry controls NA Affymetrix, Illumina [510672] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081269 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A09.9: Gastroenteritis and colitis of unspecified origin (Gene-based burden) 8,538 European ancestry cases, 379,392 European ancestry controls NA Illumina [185344] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90083528 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z48.8: Encounter for other specified postprocedural aftercare 970 European ancestry cases, 386,929 European ancestry controls NA Affymetrix, Illumina [510672] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081270 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A41: Other sepsis (Gene-based burden) 5,918 European ancestry cases, 381,545 European ancestry controls NA Illumina [185340] 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90083532 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.0: Acute gastritis 526 European ancestry cases, 387,388 European ancestry controls NA Affymetrix, Illumina [510671] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90080201 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A41.5: Sepsis due to other Gram-negative organisms (Gene-based burden) 895 European ancestry cases, 387,035 European ancestry controls NA Illumina [185344] 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90083530 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.3: Colostomy status 1,243 European ancestry cases, 386,672 European ancestry controls NA Affymetrix, Illumina [510671] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081414 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A41.9: Sepsis, unspecified organism (Gene-based burden) 4,673 European ancestry cases, 382,844 European ancestry controls NA Illumina [185339] 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90083531 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C83: Non-follicular lymphoma 1,109 European ancestry cases, 386,801 European ancestry controls NA Affymetrix, Illumina [510670] 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90079635 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.9: Malignant neoplasm of colon, unspecified (Gene-based burden) 1,360 European ancestry cases, 386,429 European ancestry controls NA Illumina [185342] 0 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90083566 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D41: Neoplasm of uncertain behavior of urinary organs 970 European ancestry cases, 386,931 European ancestry controls NA Affymetrix, Illumina [510663] 0 GCST90079698 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C19: Malignant neoplasm of rectosigmoid junction (Gene-based burden) 1,074 European ancestry cases, 386,842 European ancestry controls NA Illumina [185344] 0 rectosigmoid junction neoplasm http://purl.obolibrary.org/obo/MONDO_0002423 GCST90083568 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.2: Derangement of meniscus due to old tear or injury 12,372 European ancestry cases, 375,533 European ancestry controls NA Affymetrix, Illumina [510663] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080438 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C20: Malignant neoplasm of rectum (Gene-based burden) 1,884 European ancestry cases, 385,913 European ancestry controls NA Illumina [185341] 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90083569 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C82: Follicular lymphoma 538 European ancestry cases, 387,366 European ancestry controls NA Affymetrix, Illumina [510662] 0 follicular lymphoma http://purl.obolibrary.org/obo/MONDO_0018906 GCST90079633 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C22: Malignant neoplasm of liver and intrahepatic bile ducts (Gene-based burden) 575 European ancestry cases, 387,333 European ancestry controls NA Illumina [185344] 0 liver neoplasm http://www.ebi.ac.uk/efo/EFO_1001513 GCST90083570 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H43.1: Vitreous hemorrhage 620 European ancestry cases, 387,305 European ancestry controls NA Affymetrix, Illumina [510662] 0 vitreous hemorrhage http://www.ebi.ac.uk/efo/EFO_0008626 GCST90079910 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C25: Malignant neoplasm of pancreas (Gene-based burden) 961 European ancestry cases, 386,943 European ancestry controls NA Illumina [185344] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90083572 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K14.8: Other diseases of tongue 866 European ancestry cases, 387,037 European ancestry controls NA Affymetrix, Illumina [510662] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90080183 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C25.9: Malignant neoplasm of pancreas, unspecified (Gene-based burden) 872 European ancestry cases, 387,058 European ancestry controls NA Illumina [185344] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90083571 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.5: Mouth breathing 2,287 European ancestry cases, 385,623 European ancestry controls NA Affymetrix, Illumina [510662] 0 Abnormal pattern of respiration http://purl.obolibrary.org/obo/HP_0002793 GCST90080769 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34: Malignant neoplasm of bronchus and lung (Gene-based burden) 3,122 European ancestry cases, 384,752 European ancestry controls NA Illumina [185344] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90083576 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I31.3: Pericardial effusion (noninflammatory) 937 European ancestry cases, 386,964 European ancestry controls NA Affymetrix, Illumina [510661] 0 pericardial effusion http://purl.obolibrary.org/obo/MONDO_0001370 GCST90079988 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34.1: Malignant neoplasm of upper lobe, bronchus or lung (Gene-based burden) 1,228 European ancestry cases, 386,702 European ancestry controls NA Illumina [185344] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90083573 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K74.6: Other and unspecified cirrhosis of liver 852 European ancestry cases, 387,041 European ancestry controls NA Affymetrix, Illumina [510661] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90080285 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Monocyte count (UKB data field 30130) 418,449 European ancestry individuals 101,419 European ancestry individuals Affymetrix, Illumina [537906] 2 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90078992 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Completion status of test - Participant wanted to stop early (UKB data field 6020) (Gene-based burden) 814 European ancestry cases, 79,707 European ancestry controls NA Illumina [159840] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083396 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neutrophill count (UKB data field 30140) 418,449 European ancestry individuals 87,654 European ancestry individuals Affymetrix, Illumina [537906] 3 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90078993 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Completion status of test - Heart rate reached safety level (UKB data field 6020) (Gene-based burden) 4,620 European ancestry cases, 75,901 European ancestry controls NA Illumina [159840] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083397 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - More than half the days (UKB data field 2080) 26,703 European ancestry cases, 392,133 European ancestry controls NA Affymetrix, Illumina [537863] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90078681 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Contemplated self harm in past year (UKB data field 20486) (Gene-based burden) 4,107 European ancestry cases, 16,395 European ancestry controls NA Illumina [108017] 0 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST90082506 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - Nearly every day (UKB data field 2080) 27,214 European ancestry cases, 391,622 European ancestry controls NA Affymetrix, Illumina [537863] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90078682 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Contraindications for spirometry (UKB data field 3088) (Gene-based burden) 36,852 European ancestry cases, 392,068 European ancestry controls NA Illumina [185926] 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90083032 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - Not at all (UKB data field 2080) 204,460 European ancestry cases, 214,376 European ancestry controls NA Affymetrix, Illumina [537863] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078679 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M96: Intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified 588 European ancestry cases, 387,322 European ancestry controls NA Affymetrix, Illumina [510670] 0 musculoskeletal system disease http://www.ebi.ac.uk/efo/EFO_0009676 GCST90080570 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B00: Herpesviral [herpes simplex] infections (Gene-based burden) 1,285 European ancestry cases, 382,676 European ancestry controls NA Illumina [185296] 0 Herpesviridae infectious disease http://www.ebi.ac.uk/efo/EFO_0007309 GCST90083534 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T51: Toxic effect of alcohol 1,105 European ancestry cases, 386,807 European ancestry controls NA Affymetrix, Illumina [510670] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081063 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B02: Zoster [herpes zoster] (Gene-based burden) 2,991 European ancestry cases, 372,592 European ancestry controls NA Illumina [185180] 0 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST90083535 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H43.8: Other disorders of vitreous body 881 European ancestry cases, 387,028 European ancestry controls NA Affymetrix, Illumina [510669] 0 vitreous body disease http://www.ebi.ac.uk/efo/EFO_0008624 GCST90079911 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B07: Viral warts (Gene-based burden) 4,761 European ancestry cases, 372,404 European ancestry controls NA Illumina [185178] 0 common wart http://www.ebi.ac.uk/efo/EFO_0009662 GCST90083536 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28.8: Other specified disorders of kidney and ureter 830 European ancestry cases, 387,074 European ancestry controls NA Affymetrix, Illumina [510669] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90080593 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B34: Viral infection of unspecified site (Gene-based burden) 4,826 European ancestry cases, 371,590 European ancestry controls NA Illumina [185159] 0 viral disease http://www.ebi.ac.uk/efo/EFO_0000763 GCST90083538 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.4: Personal history of malignant neoplasm of genital organs 5,672 European ancestry cases, 382,236 European ancestry controls 2,961 European ancestry cases, 33,898 European ancestry controls Affymetrix, Illumina [510669] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90081350 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B34.9: Viral infection, unspecified (Gene-based burden) 3,710 European ancestry cases, 378,790 European ancestry controls NA Illumina [185281] 0 viral disease http://www.ebi.ac.uk/efo/EFO_0000763 GCST90083537 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.8: Personal history of malignant neoplasms of other organs and systems 7,665 European ancestry cases, 380,238 European ancestry controls 8,152 European ancestry cases, 33,898 European ancestry controls Affymetrix, Illumina [510669] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90081353 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B35: Dermatophytosis (Gene-based burden) 10,336 European ancestry cases, 359,321 European ancestry controls NA Illumina [185079] 0 dermatophytosis http://purl.obolibrary.org/obo/MONDO_0004678 GCST90083539 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.8: Presence of other cardiac and vascular implants and grafts 2,644 European ancestry cases, 385,255 European ancestry controls NA Affymetrix, Illumina [510669] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081424 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B36: Other superficial mycoses (Gene-based burden) 880 European ancestry cases, 383,055 European ancestry controls NA Illumina [185248] 0 cutaneous mycosis http://purl.obolibrary.org/obo/MONDO_0000254 GCST90083540 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G43.9: Migraine, unspecified 3,383 European ancestry cases, 384,515 European ancestry controls NA Affymetrix, Illumina [510668] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90079826 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37: Candidiasis (Gene-based burden) 8,778 European ancestry cases, 363,381 European ancestry controls NA Illumina [185125] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90083546 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.3: Blepharochalasis 883 European ancestry cases, 387,020 European ancestry controls NA Affymetrix, Illumina [510668] 0 Ascher syndrome http://purl.obolibrary.org/obo/MONDO_0007198 GCST90079870 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.0: Candidal stomatitis (Gene-based burden) 1,312 European ancestry cases, 386,618 European ancestry controls NA Illumina [185344] 0 stomatitis http://www.ebi.ac.uk/efo/EFO_0009688 GCST90083541 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Chlamydia trachomatis (UKB data field 23070) (Gene-based burden) 1,732 European ancestry cases, 6,809 European ancestry controls NA Illumina [70714] 0 Chlamydia trachomatis seropositivity http://www.ebi.ac.uk/efo/EFO_0009330 GCST90082885 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean platelet thrombocyte volume (UKB data field 30100) 419,184 European ancestry individuals NA Affymetrix, Illumina [538529] 24 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90078989 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coronary artery disease (Gene-based burden) 28,605 European ancestry cases, 254,598 European ancestry controls NA Illumina [182940] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90085452 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Father still alive (UKB data field 1797) 96,906 European ancestry cases, 322,692 European ancestry controls NA Affymetrix, Illumina [538493] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90077613 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coronary artery disease - loose (Gene-based burden) 33,971 European ancestry cases, 353,040 European ancestry controls NA Illumina [185325] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90085451 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Chronic bronchitis emphysema (UKB data field 20107) 44,472 European ancestry cases, 375,126 European ancestry controls NA Affymetrix, Illumina [538493] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078261 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 21 Do not know group 2 (UKB data field 20107) 34,809 European ancestry cases, 384,788 European ancestry controls NA Affymetrix, Illumina [538492] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078266 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - Definitely an evening person (UKB data field 1180) (Gene-based burden) 36,316 European ancestry cases, 352,014 European ancestry controls NA Illumina [185326] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90081562 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 27 None of the above group 2 (UKB data field 20107) 284,370 European ancestry cases, 135,227 European ancestry controls NA Affymetrix, Illumina [538492] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078267 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - More a morning than evening person (UKB data field 1180) (Gene-based burden) 145,271 European ancestry cases, 243,059 European ancestry controls NA Illumina [185326] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90081560 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Platelet crit (UKB data field 30090) 419,060 European ancestry individuals NA Affymetrix, Illumina [538426] 11 platelet crit http://www.ebi.ac.uk/efo/EFO_0007985 GCST90078988 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - More an evening than a morning person (UKB data field 1180) (Gene-based burden) 114,330 European ancestry cases, 274,000 European ancestry controls NA Illumina [185326] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90081561 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Platelet distribution width (UKB data field 30110) 419,059 European ancestry individuals NA Affymetrix, Illumina [538425] 15 platelet component distribution width http://www.ebi.ac.uk/efo/EFO_0007984 GCST90078990 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic kidney disease (Gene-based burden) 7,613 European ancestry cases, 354,119 European ancestry controls NA Illumina [184876] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90085453 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Creatinine enzymatic in urine (UKB data field 30510) 419,176 European ancestry individuals NA Affymetrix, Illumina [538260] 0 creatinine clearance measurement http://www.ebi.ac.uk/efo/EFO_0007934 GCST90079008 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Human Cytomegalovirus (UKB data field 23054) (Gene-based burden) 4,835 European ancestry cases, 3,706 European ancestry controls NA Illumina [70714] 0 cytomegalovirus seropositivity http://www.ebi.ac.uk/efo/EFO_0007037 GCST90082875 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sensitivity hurt feelings (UKB data field 1950) 236,796 European ancestry cases, 182,655 European ancestry controls NA Affymetrix, Illumina [538177] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90077621 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coffee consumed (UKB data field 100240) (Gene-based burden) 144,030 European ancestry cases, 41,614 European ancestry controls NA Illumina [177616] 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90081543 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Basophill percentage (UKB data field 30220) 418,454 European ancestry individuals 99,227 European ancestry individuals Affymetrix, Illumina [537915] 0 basophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007992 GCST90078999 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative body size at age 10 - About average (UKB data field 1687) (Gene-based burden) 219,264 European ancestry cases, 204,348 European ancestry controls NA Illumina [185848] 0 comparative body size at age 10, self-reported http://www.ebi.ac.uk/efo/EFO_0009819 GCST90081576 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eosinophill percentage (UKB data field 30210) 418,454 European ancestry individuals 101,190 European ancestry individuals Affymetrix, Illumina [537915] 3 eosinophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007991 GCST90078998 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative body size at age 10 - Plumper (UKB data field 1687) (Gene-based burden) 68,629 European ancestry cases, 354,983 European ancestry controls NA Illumina [185848] 0 comparative body size at age 10, self-reported http://www.ebi.ac.uk/efo/EFO_0009819 GCST90081575 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lymphocyte percentage (UKB data field 30180) 418,454 European ancestry individuals 102,034 European ancestry individuals Affymetrix, Illumina [537915] 4 lymphocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007993 GCST90078995 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative body size at age 10 - Thinner (UKB data field 1687) (Gene-based burden) 141,504 European ancestry cases, 282,108 European ancestry controls NA Illumina [185848] 0 comparative body size at age 10, self-reported http://www.ebi.ac.uk/efo/EFO_0009819 GCST90081574 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Monocyte percentage (UKB data field 30190) 418,454 European ancestry individuals 102,628 European ancestry individuals Affymetrix, Illumina [537915] 4 monocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007989 GCST90078996 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative height size at age 10 - About average (UKB data field 1697) (Gene-based burden) 231,189 European ancestry cases, 192,786 European ancestry controls NA Illumina [185853] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90081579 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neutrophill percentage (UKB data field 30200) 418,454 European ancestry individuals 102,380 European ancestry individuals Affymetrix, Illumina [537915] 2 neutrophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007990 GCST90078997 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative height size at age 10 - Shorter (UKB data field 1697) (Gene-based burden) 87,597 European ancestry cases, 336,378 European ancestry controls NA Illumina [185853] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90081577 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eosinophill count (UKB data field 30150) 418,449 European ancestry individuals 100,249 European ancestry individuals Affymetrix, Illumina [537906] 3 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90078994 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative height size at age 10 - Taller (UKB data field 1697) (Gene-based burden) 109,627 European ancestry cases, 314,348 European ancestry controls NA Illumina [185853] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90081578 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lymphocyte count (UKB data field 30120) 418,449 European ancestry individuals 101,441 European ancestry individuals Affymetrix, Illumina [537906] 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90078991 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Completion status of test - Fully completed (UKB data field 6020) (Gene-based burden) 74,782 European ancestry cases, 5,739 European ancestry controls NA Illumina [159840] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083395 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.8: Other age-related cataract 2,425 European ancestry cases, 385,472 European ancestry controls NA Affymetrix, Illumina [510668] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90079887 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.3: Candidiasis of vulva and vagina (Gene-based burden) 2,475 European ancestry cases, 203,953 European ancestry controls NA Illumina [179601] 0 vulvovaginal candidiasis http://www.ebi.ac.uk/efo/EFO_0007543 GCST90083542 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.3: Other meniscus derangements 4,543 European ancestry cases, 383,357 European ancestry controls NA Affymetrix, Illumina [510668] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080443 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.4: Candidiasis of other urogenital sites (Gene-based burden) 676 European ancestry cases, 383,576 European ancestry controls NA Illumina [185285] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90083544 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.81: Other internal derangements of knee 600 European ancestry cases, 387,330 European ancestry controls NA Affymetrix, Illumina [510668] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080445 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.49: Other urogenital candidiasis (Gene-based burden) 512 European ancestry cases, 384,170 European ancestry controls NA Illumina [185285] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90083543 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W26: Contact with other sharp objects 568 European ancestry cases, 387,347 European ancestry controls NA Affymetrix, Illumina [510668] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081124 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.8: Candidiasis of other sites (Gene-based burden) 1,130 European ancestry cases, 386,725 European ancestry controls NA Illumina [185341] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90083545 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.3: Dependence on wheelchair 762 European ancestry cases, 387,143 European ancestry controls NA Affymetrix, Illumina [510668] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081443 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95: Streptococcus, Staphylococcus, and Enterococcus as the cause of diseases classified elsewhere (Gene-based burden) 5,108 European ancestry cases, 382,689 European ancestry controls NA Illumina [185341] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083550 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.4: Other and unspecified malignant neoplasm of skin of scalp and neck 1,835 European ancestry cases, 386,072 European ancestry controls NA Affymetrix, Illumina [510667] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079597 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95.4: Other streptococcus as the cause of diseases classified elsewhere (Gene-based burden) 830 European ancestry cases, 387,100 European ancestry controls NA Illumina [185344] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083547 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.0: Glaucoma suspect 1,355 European ancestry cases, 386,553 European ancestry controls NA Affymetrix, Illumina [510667] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90079905 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95.6: Staphylococcus aureus as the cause of diseases classified elsewhere (Gene-based burden) 2,837 European ancestry cases, 385,030 European ancestry controls NA Illumina [185342] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083548 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I70.2: Atherosclerosis of native arteries of the extremities 1,065 European ancestry cases, 386,835 European ancestry controls NA Affymetrix, Illumina [510667] 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90080045 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95.7: Other staphylococcus as the cause of diseases classified elsewhere (Gene-based burden) 618 European ancestry cases, 387,312 European ancestry controls NA Illumina [185344] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083549 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.30: Other meniscus derangements, unspecified meniscus 591 European ancestry cases, 387,307 European ancestry controls NA Affymetrix, Illumina [510667] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080439 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96: Other bacterial agents as the cause of diseases classified elsewhere (Gene-based burden) 11,084 European ancestry cases, 375,265 European ancestry controls NA Illumina [185324] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083555 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48.0: Spinal stenosis 5,125 European ancestry cases, 382,789 European ancestry controls NA Affymetrix, Illumina [510667] 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90080489 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.1: Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified elsewhere (Gene-based burden) 525 European ancestry cases, 387,405 European ancestry controls NA Illumina [185344] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083551 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.9: Surgical procedure, unspecified as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 636 European ancestry cases, 387,270 European ancestry controls NA Affymetrix, Illumina [510667] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081164 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.2: Escherichia coli [E. coli ] as the cause of diseases classified elsewhere (Gene-based burden) 3,844 European ancestry cases, 384,028 European ancestry controls NA Illumina [185344] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083552 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.8: Other visual disturbances 934 European ancestry cases, 386,978 European ancestry controls NA Affymetrix, Illumina [510666] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90079921 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.5: Pseudomonas (aeruginosa) (mallei) (pseudomallei) as the cause of diseases classified elsewhere (Gene-based burden) 1,140 European ancestry cases, 386,786 European ancestry controls NA Illumina [185344] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083553 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease (Gene-based burden) 14,114 European ancestry cases, 315,430 European ancestry controls NA Illumina [184175] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90085455 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - Several days (UKB data field 2080) 180,228 European ancestry cases, 238,608 European ancestry controls NA Affymetrix, Illumina [537863] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90078680 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease - composite (Gene-based burden) 14,114 European ancestry cases, 330,697 European ancestry controls NA Illumina [184487] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90085454 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - About once a month (UKB data field 2110) 24,709 European ancestry cases, 394,103 European ancestry controls NA Affymetrix, Illumina [537756] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90078842 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal hysteresis left (UKB data field 5264) (Gene-based burden) 105,697 European ancestry individuals NA Illumina [167144] 0 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST90083325 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - About once a week (UKB data field 2110) 50,348 European ancestry cases, 368,464 European ancestry controls NA Affymetrix, Illumina [537756] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90078843 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal hysteresis right (UKB data field 5256) (Gene-based burden) 105,888 European ancestry individuals NA Illumina [167136] 0 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST90083321 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - Almost daily (UKB data field 2110) 232,393 European ancestry cases, 186,419 European ancestry controls NA Affymetrix, Illumina [537756] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90078845 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal power (Gene-based burden) 103,531 European ancestry individuals NA Illumina [166559] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085523 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - Never or almost never (UKB data field 2110) 64,936 European ancestry cases, 353,876 European ancestry controls NA Affymetrix, Illumina [537756] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90078840 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal power - started wearing glasses or contacts before 40 (Gene-based burden) 47,125 European ancestry individuals NA Illumina [142420] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085524 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - Once every few months (UKB data field 2110) 25,583 European ancestry cases, 393,229 European ancestry controls NA Affymetrix, Illumina [537756] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90078841 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal resistance factor left (UKB data field 5265) (Gene-based burden) 105,697 European ancestry individuals NA Illumina [167144] 0 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST90083326 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - 2 to 4 times a week (UKB data field 2110) 44,658 European ancestry cases, 374,154 European ancestry controls NA Affymetrix, Illumina [537756] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90078844 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry angle left (UKB data field 5111) (Gene-based burden) 105,888 European ancestry individuals NA Illumina [167136] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083322 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Potassium in urine (UKB data field 30520) 418,307 European ancestry individuals NA Affymetrix, Illumina [537539] 0 urinary potassium measurement http://www.ebi.ac.uk/efo/EFO_0010952 GCST90079009 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm left (first instance) 90,788 European ancestry individuals NA Illumina [163519] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085460 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sodium in urine (UKB data field 30530) 418,293 European ancestry individuals NA Affymetrix, Illumina [537505] 0 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST90079010 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm right (first instance) 90,792 European ancestry individuals NA Illumina [163521] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085461 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tea intake (UKB data field 1488) 417,958 European ancestry individuals NA Affymetrix, Illumina [537078] 1 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST90077587 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm left (first instance) 78,888 European ancestry individuals NA Illumina [159730] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085462 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tense / highly strung (UKB data field 1990) 75,379 European ancestry cases, 342,726 European ancestry controls NA Affymetrix, Illumina [537047] 0 feeling tense measurement http://www.ebi.ac.uk/efo/EFO_0009596 GCST90077625 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm right (first instance) 79,752 European ancestry individuals NA Illumina [160004] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085463 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - More than half the days (UKB data field 2060) 11,544 European ancestry cases, 405,923 European ancestry controls NA Affymetrix, Illumina [536502] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078673 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm left (Gene-based burden) 103,531 European ancestry individuals NA Illumina [166559] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085464 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Calcium levels (UKB data field 30680) (Gene-based burden) 378,246 European ancestry individuals NA Illumina [185104] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90083009 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Diabetes (UKB data field 20107) 36,789 European ancestry cases, 382,809 European ancestry controls NA Affymetrix, Illumina [538493] 1 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078263 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cancer (UKB data field 20001) (Gene-based burden) 613 European ancestry cases, 39,001 European ancestry controls NA Illumina [134284] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90081630 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Heart disease (UKB data field 20107) 127,319 European ancestry cases, 292,279 European ancestry controls NA Affymetrix, Illumina [538493] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078257 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain due to walking ceases when standing still (UKB data field 3616) (Gene-based burden) 21,127 European ancestry cases, 4,846 European ancestry controls NA Illumina [118306] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90083053 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - High blood pressure (UKB data field 20107) 87,674 European ancestry cases, 331,924 European ancestry controls NA Affymetrix, Illumina [538493] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078262 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain felt during physical activity (UKB data field 6015) (Gene-based burden) 2,964 European ancestry cases, 77,501 European ancestry controls NA Illumina [159755] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90083392 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Stroke (UKB data field 20107) 60,161 European ancestry cases, 359,437 European ancestry controls NA Affymetrix, Illumina [538493] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078258 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain felt outside physical activity (UKB data field 6016) (Gene-based burden) 2,532 European ancestry cases, 78,491 European ancestry controls NA Illumina [159994] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90083393 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Alzheimers disease dementia (UKB data field 20107) 20,299 European ancestry cases, 399,299 European ancestry controls NA Affymetrix, Illumina [538493] 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90078253 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain or discomfort (UKB data field 2335) (Gene-based burden) 71,172 European ancestry cases, 355,555 European ancestry controls NA Illumina [185878] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90082921 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 11 Do not know group 1 (UKB data field 20107) 29,911 European ancestry cases, 389,687 European ancestry controls NA Affymetrix, Illumina [538493] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078264 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain or discomfort walking normally (UKB data field 3606) (Gene-based burden) 12,469 European ancestry cases, 58,080 European ancestry controls NA Illumina [155180] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90083052 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - 17 None of the above group 1 (UKB data field 20107) 142,509 European ancestry cases, 277,089 European ancestry controls NA Affymetrix, Illumina [538493] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078265 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain or discomfort when walking uphill or hurrying (UKB data field 3751) (Gene-based burden) 15,414 European ancestry cases, 41,575 European ancestry controls NA Illumina [147900] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90083057 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Bowel cancer (UKB data field 20107) 22,536 European ancestry cases, 397,061 European ancestry controls NA Affymetrix, Illumina [538492] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078260 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Childhood asthma vs adult asthma (Gene-based burden) 16,952 European ancestry cases, 26,201 European ancestry controls NA Illumina [138037] 0 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90085458 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Lung cancer (UKB data field 20107) 35,172 European ancestry cases, 384,425 European ancestry controls NA Affymetrix, Illumina [538492] 1 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078259 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Childhood asthma vs allergic disease (Gene-based burden) 16,952 European ancestry cases, 280,473 European ancestry controls NA Illumina [183205] 0 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90085459 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Parkinsons disease (UKB data field 20107) 9,552 European ancestry cases, 410,045 European ancestry controls NA Affymetrix, Illumina [538492] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078254 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cholesterol levels (UKB data field 30690) (Gene-based burden) 412,075 European ancestry individuals NA Illumina [185667] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90083010 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Severe depression (UKB data field 20107) 14,714 European ancestry cases, 404,883 European ancestry controls NA Affymetrix, Illumina [538492] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078255 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cholesterol lowering medication use (UKB data field 6177) (Gene-based burden) 49,091 European ancestry cases, 20,382 European ancestry controls NA Illumina [153090] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083472 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of father - Prostate cancer (UKB data field 20107) 29,430 European ancestry cases, 390,167 European ancestry controls NA Affymetrix, Illumina [538492] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078256 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - Definitely a morning person (UKB data field 1180) (Gene-based burden) 107,453 European ancestry cases, 280,877 European ancestry controls NA Illumina [185326] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90081559 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A49: Bacterial infection of unspecified site (Gene-based burden) 1,117 European ancestry cases, 385,841 European ancestry controls NA Illumina [185326] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90083533 Exome-wide sequencing 2021-03-09 32341752 Kohaar I 2020-04-14 Oncotarget www.ncbi.nlm.nih.gov/pubmed/32341752 Association of germline genetic variants with TMPRSS2-ERG fusion status in prostate cancer. Prostate cancer 216 African American cases, 105 European ancestry cases NA Illumina [478299] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011256 Targeted genotyping array [Oncoarray] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49.3: Ventricular premature depolarization 630 European ancestry cases, 387,300 European ancestry controls NA Affymetrix, Illumina [510688] 0 ventricular ectopy http://www.ebi.ac.uk/efo/EFO_0009276 GCST90080016 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had known person concerned about or recommend reduction of alcohol consumption but not in the last year (UKB data field 20405) (Gene-based burden) 6,352 European ancestry cases, 133,151 European ancestry controls NA Illumina [172113] 0 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST90082389 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49.5: Sick sinus syndrome 612 European ancestry cases, 387,318 European ancestry controls NA Affymetrix, Illumina [510688] 0 sick sinus syndrome http://purl.obolibrary.org/obo/MONDO_0001823 GCST90080017 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had known person concerned about or recommend reduction of alcohol consumption during the last year (UKB data field 20405) (Gene-based burden) 5,724 European ancestry cases, 133,779 European ancestry controls NA Illumina [172113] 0 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST90082390 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50.0: Congestive heart failure 3,182 European ancestry cases, 384,748 European ancestry controls NA Affymetrix, Illumina [510688] 0 congestive heart failure http://www.ebi.ac.uk/efo/EFO_0000373 GCST90080020 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had laser eye surgery - Both eyes (UKB data field 5325) (Gene-based burden) 1,848 European ancestry cases, 6,743 European ancestry controls NA Illumina [71433] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90083329 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50.9: Heart failure, unspecified 2,407 European ancestry cases, 385,523 European ancestry controls 7,700 European ancestry cases, 93,882 European ancestry controls Affymetrix, Illumina [510688] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90080022 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had period extreme irritability (UKB data field 20502) (Gene-based burden) 35,638 European ancestry cases, 99,747 European ancestry controls NA Illumina [171451] 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90082543 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51.8: Other ill-defined heart diseases 2,078 European ancestry cases, 385,851 European ancestry controls NA Affymetrix, Illumina [510688] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90080025 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had period of mania excitability (UKB data field 20501) (Gene-based burden) 5,876 European ancestry cases, 130,604 European ancestry controls NA Illumina [171662] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082542 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I63.5: Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries 552 European ancestry cases, 387,378 European ancestry controls NA Affymetrix, Illumina [510688] 0 cerebral infarction http://purl.obolibrary.org/obo/MONDO_0002679 GCST90080033 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had prolonged feelings of sadness or depression (UKB data field 20446) (Gene-based burden) 76,460 European ancestry cases, 62,905 European ancestry controls NA Illumina [172089] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082453 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I67.8: Other specified cerebrovascular diseases 1,481 European ancestry cases, 386,449 European ancestry controls NA Affymetrix, Illumina [510688] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90080039 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had prolonged loss of interest in normal activities (UKB data field 20441) (Gene-based burden) 55,126 European ancestry cases, 84,200 European ancestry controls NA Illumina [172079] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082451 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I69.4: Sequelae of stroke, not specified as haemorrhage or infarction 1,221 European ancestry cases, 386,709 European ancestry controls NA Affymetrix, Illumina [510688] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90080042 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had prostate specific antigen PSA test (UKB data field 2365) (Gene-based burden) 62,851 European ancestry cases, 124,707 European ancestry controls NA Illumina [176749] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90082923 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73.0: Raynaud's syndrome 1,538 European ancestry cases, 386,392 European ancestry controls NA Affymetrix, Illumina [510688] 0 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90080049 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever heard an unreal voice (UKB data field 20463) (Gene-based burden) 2,438 European ancestry cases, 136,626 European ancestry controls NA Illumina [172054] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082488 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84: Haemorrhoids 27,106 European ancestry cases, 360,824 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080074 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever highly irritable - argumentative for 2 days (UKB data field 4653) (Gene-based burden) 30,880 European ancestry cases, 143,261 European ancestry controls NA Illumina [176768] 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90083201 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.1: Internal haemorrhoids with other complications 2,850 European ancestry cases, 385,080 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080067 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever manic hyper for 2 days (UKB data field 4642) (Gene-based burden) 9,621 European ancestry cases, 164,125 European ancestry controls NA Illumina [176741] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083200 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.2: Internal haemorrhoids without complication 4,833 European ancestry cases, 383,097 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080068 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever physically dependent on alcohol (UKB data field 20404) (Gene-based burden) 840 European ancestry cases, 2,203 European ancestry controls NA Illumina [34270] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90082388 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.4: External haemorrhoids with other complications 534 European ancestry cases, 387,396 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080069 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever prescribed a medication for unusual or psychotic experiences (UKB data field 20466) (Gene-based burden) 768 European ancestry cases, 6,064 European ancestry controls NA Illumina [62522] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082489 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.5: External haemorrhoids without complication 1,062 European ancestry cases, 386,868 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080070 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever seen an unreal vision (UKB data field 20471) (Gene-based burden) 4,462 European ancestry cases, 133,755 European ancestry controls NA Illumina [171876] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082493 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.6: Residual haemorrhoidal skin tags 4,208 European ancestry cases, 383,722 European ancestry controls NA Affymetrix, Illumina [510688] 0 Skin tags http://purl.obolibrary.org/obo/HP_0010609 GCST90080071 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever self harmed (UKB data field 20480) (Gene-based burden) 6,056 European ancestry cases, 133,254 European ancestry controls NA Illumina [172093] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90082498 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.8: Unspecified haemorrhoids with other complications 3,859 European ancestry cases, 384,071 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080072 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever smoked (UKB data field 20160) (Gene-based burden) 263,214 European ancestry cases, 166,087 European ancestry controls NA Illumina [185927] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90082310 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.9: Unspecified haemorrhoids without complication 14,954 European ancestry cases, 372,976 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080073 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever sought or received professional help for mental distress (UKB data field 20499) (Gene-based burden) 54,821 European ancestry cases, 84,434 European ancestry controls NA Illumina [172058] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90082540 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18.0: Bronchopneumonia, unspecified organism 1,056 European ancestry cases, 386,874 European ancestry controls NA Affymetrix, Illumina [510688] 0 bronchopneumonia http://www.ebi.ac.uk/efo/EFO_0007184 GCST90080095 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever stopped smoking for 6 months (UKB data field 2907) (Gene-based burden) 47,242 European ancestry cases, 60,216 European ancestry controls NA Illumina [166280] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90082956 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33.0: Polyp of nasal cavity 1,256 European ancestry cases, 386,674 European ancestry controls NA Affymetrix, Illumina [510688] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90080110 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever suffered mental distress preventing usual activities (UKB data field 20500) (Gene-based burden) 46,079 European ancestry cases, 91,780 European ancestry controls NA Illumina [171852] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90082541 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33.8: Other polyp of sinus 740 European ancestry cases, 387,190 European ancestry controls NA Affymetrix, Illumina [510688] 0 polyp http://www.ebi.ac.uk/efo/EFO_0000662 GCST90080111 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - 11 to 100 times (UKB data field 20453) (Gene-based burden) 6,210 European ancestry cases, 133,301 European ancestry controls NA Illumina [172118] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90082460 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33.9: Nasal polyp, unspecified 2,073 European ancestry cases, 385,857 European ancestry controls NA Affymetrix, Illumina [510688] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90080112 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - more than 100 times (UKB data field 20453) (Gene-based burden) 3,721 European ancestry cases, 135,790 European ancestry controls NA Illumina [172118] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90082461 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34.3: Hypertrophy of nasal turbinates 1,949 European ancestry cases, 385,981 European ancestry controls NA Affymetrix, Illumina [510688] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080115 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - 1 to 2 times (UKB data field 20453) (Gene-based burden) 13,223 European ancestry cases, 126,288 European ancestry controls NA Illumina [172118] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90082458 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.0: Chronic obstructive pulmonary disease with acute lower respiratory infection 3,295 European ancestry cases, 384,635 European ancestry controls NA Affymetrix, Illumina [510688] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90080129 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken cannabis - 3 to 10 times (UKB data field 20453) (Gene-based burden) 7,724 European ancestry cases, 131,787 European ancestry controls NA Illumina [172118] 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90082459 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.1: Chronic obstructive pulmonary disease with (acute) exacerbation 1,520 European ancestry cases, 386,410 European ancestry controls NA Affymetrix, Illumina [510688] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90080130 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever taken oral contraceptive pill (UKB data field 2784) (Gene-based burden) 191,547 European ancestry cases, 41,586 European ancestry controls NA Illumina [181143] 0 contraception http://www.ebi.ac.uk/efo/EFO_0009520 GCST90082945 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.8: Other specified chronic obstructive pulmonary disease 878 European ancestry cases, 387,052 European ancestry controls NA Affymetrix, Illumina [510688] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90080131 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever talked to a health professional about unusual or psychotic experiences (UKB data field 20477) (Gene-based burden) 1,463 European ancestry cases, 5,384 European ancestry controls NA Illumina [62585] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082495 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.0: Predominantly allergic asthma 815 European ancestry cases, 387,115 European ancestry controls NA Affymetrix, Illumina [510688] 0 atopic asthma http://www.ebi.ac.uk/efo/EFO_0010638 GCST90080134 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever thought that life not worth living more than once (UKB data field 20479) (Gene-based burden) 24,195 European ancestry cases, 114,587 European ancestry controls NA Illumina [171997] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082497 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J69.0: Pneumonitis due to inhalation of food and vomit 1,101 European ancestry cases, 386,829 European ancestry controls NA Affymetrix, Illumina [510688] 0 pneumonitis http://www.ebi.ac.uk/efo/EFO_1001991 GCST90080143 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.3: Mental and behavioural disorders due to use of alcohol, withdrawal state (Gene-based burden) 847 European ancestry cases, 387,083 European ancestry controls NA Illumina [185344] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90083777 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K85.9: Acute pancreatitis, unspecified 708 European ancestry cases, 387,020 European ancestry controls NA Affymetrix, Illumina [510502] 0 acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1000652 GCST90080309 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.9: Alcohol use, unspecified (Gene-based burden) 109,309 European ancestry cases, 235,868 European ancestry controls NA Illumina [184558] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90083778 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50.1: Left ventricular failure, unspecified 4,762 European ancestry cases, 382,963 European ancestry controls 543 European ancestry cases, 93,898 European ancestry controls Affymetrix, Illumina [510501] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90080021 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17: Nicotine dependence (Gene-based burden) 32,828 European ancestry cases, 337,667 European ancestry controls NA Illumina [185091] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90083784 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.0: Fracture of upper end of ulna 953 European ancestry cases, 386,775 European ancestry controls NA Affymetrix, Illumina [510501] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080985 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.1: Mental and behavioural disorders due to use of tobacco, harmful use (Gene-based burden) 14,902 European ancestry cases, 373,028 European ancestry controls NA Illumina [185344] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90083780 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C85: Other specified and unspecified types of non-Hodgkin lymphoma 1,579 European ancestry cases, 386,126 European ancestry controls NA Affymetrix, Illumina [510499] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90079638 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.2: Nicotine dependence (Gene-based burden) 5,766 European ancestry cases, 369,408 European ancestry controls NA Illumina [185167] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90083783 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I70: Atherosclerosis 1,790 European ancestry cases, 385,917 European ancestry controls NA Affymetrix, Illumina [510499] 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90080046 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.20: Nicotine dependence, unspecified (Gene-based burden) 4,932 European ancestry cases, 370,207 European ancestry controls NA Illumina [185167] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90083782 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.67: Pain in foot and toes 724 European ancestry cases, 386,976 European ancestry controls NA Affymetrix, Illumina [510499] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90080548 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.201.: Nicotine dependence, unspecified, in remission (Gene-based burden) 4,932 European ancestry cases, 370,207 European ancestry controls NA Illumina [185167] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90083781 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.0: Fall on same level from slipping, tripping and stumbling without subsequent striking against object 2,287 European ancestry cases, 385,443 European ancestry controls NA Affymetrix, Illumina [510498] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081101 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F20: Schizophrenia (Gene-based burden) 741 European ancestry cases, 387,059 European ancestry controls NA Illumina [185344] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90083786 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33.2: Serous retinal detachment 1,160 European ancestry cases, 386,573 European ancestry controls NA Affymetrix, Illumina [510492] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90079895 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F20.9: Schizophrenia, unspecified (Gene-based burden) 564 European ancestry cases, 387,292 European ancestry controls NA Illumina [185344] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90083785 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD SR: Ankylosing spondylitis 1,476 European ancestry cases, 386,233 European ancestry controls NA Affymetrix, Illumina [510490] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90079535 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F31: Bipolar disorder (Gene-based burden) 1,355 European ancestry cases, 386,380 European ancestry controls NA Illumina [185344] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90083788 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J84: Other interstitial pulmonary diseases 1,577 European ancestry cases, 386,114 European ancestry controls NA Affymetrix, Illumina [510489] 0 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90080147 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F31.9: Bipolar disorder, unspecified (Gene-based burden) 1,108 European ancestry cases, 386,721 European ancestry controls NA Illumina [185344] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90083787 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I60.9: Nontraumatic subarachnoid hemorrhage, unspecified 701 European ancestry cases, 387,022 European ancestry controls NA Affymetrix, Illumina [510488] 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90080028 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79: Secondary malignant neoplasm of other and unspecified sites 5,376 European ancestry cases, 382,352 European ancestry controls 1,352 European ancestry cases, 121,433 European ancestry controls Affymetrix, Illumina [510508] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079629 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F05.9: Delirium, unspecified (Gene-based burden) 1,083 European ancestry cases, 386,847 European ancestry controls NA Illumina [185344] 0 delirium http://www.ebi.ac.uk/efo/EFO_0009267 GCST90083771 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N35: Urethral stricture 3,910 European ancestry cases, 383,819 European ancestry controls NA Affymetrix, Illumina [510508] 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90080609 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10: Alcohol related disorders (Gene-based burden) 114,302 European ancestry cases, 230,584 European ancestry controls NA Illumina [184535] 0 alcohol-related disorders http://purl.obolibrary.org/obo/MONDO_0021698 GCST90083779 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I35.0: Nonrheumatic aortic (valve) stenosis 2,514 European ancestry cases, 385,181 European ancestry controls NA Affymetrix, Illumina [510505] 0 aortic stenosis http://www.ebi.ac.uk/efo/EFO_0000266 GCST90079994 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.0: Mental and behavioural disorders due to use of alcohol, acute intoxication (Gene-based burden) 2,064 European ancestry cases, 385,866 European ancestry controls NA Illumina [185344] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90083773 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I80.2: Phlebitis and thrombophlebitis of other and unspecified deep vessels of lower extremities 3,776 European ancestry cases, 383,943 European ancestry controls NA Affymetrix, Illumina [510504] 0 Phlebitis, Thrombophlebitis http://www.ebi.ac.uk/efo/EFO_1001395, http://purl.obolibrary.org/obo/HP_0004418 GCST90080058 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.1: Alcohol abuse (Gene-based burden) 4,296 European ancestry cases, 381,055 European ancestry controls NA Illumina [185307] 0 alcohol abuse http://purl.obolibrary.org/obo/MONDO_0002046 GCST90083775 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B97: Viral agents as the cause of diseases classified elsewhere 684 European ancestry cases, 387,059 European ancestry controls NA Affymetrix, Illumina [510503] 0 viral disease http://www.ebi.ac.uk/efo/EFO_0000763 GCST90079570 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.10: Alcohol abuse, uncomplicated (Gene-based burden) 624 European ancestry cases, 384,617 European ancestry controls NA Illumina [185307] 0 alcohol abuse http://purl.obolibrary.org/obo/MONDO_0002046 GCST90083774 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01: Fall on same level from slipping, tripping and stumbling 7,826 European ancestry cases, 379,915 European ancestry controls NA Affymetrix, Illumina [510503] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081105 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.2: Alcohol dependence (Gene-based burden) 2,395 European ancestry cases, 384,707 European ancestry controls NA Illumina [185313] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90083776 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18.1: Lobar pneumonia, unspecified organism 8,262 European ancestry cases, 379,453 European ancestry controls NA Affymetrix, Illumina [510502] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90080096 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I42.0: Dilated cardiomyopathy 858 European ancestry cases, 387,072 European ancestry controls 748 European ancestry cases, 94,883 European ancestry controls Affymetrix, Illumina [510688] 0 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST90079998 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had bowel cancer screening (UKB data field 2345) (Gene-based burden) 156,242 European ancestry cases, 268,165 European ancestry controls NA Illumina [185840] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90082922 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I42.9: Cardiomyopathy, unspecified 681 European ancestry cases, 387,249 European ancestry controls 1,031 European ancestry cases, 94,883 European ancestry controls Affymetrix, Illumina [510688] 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST90079999 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had breast cancer screening mammogram (UKB data field 2674) (Gene-based burden) 192,912 European ancestry cases, 40,420 European ancestry controls NA Illumina [181119] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90082941 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.0: Atrioventricular block, first degree 1,545 European ancestry cases, 386,385 European ancestry controls NA Affymetrix, Illumina [510688] 0 First degree atrioventricular block http://purl.obolibrary.org/obo/HP_0011705 GCST90080001 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had cataract surgery - Both eyes (UKB data field 5324) (Gene-based burden) 1,531 European ancestry cases, 7,169 European ancestry controls NA Illumina [72009] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90083328 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I45.1: Other and unspecified right bundle-branch block 2,241 European ancestry cases, 385,689 European ancestry controls NA Affymetrix, Illumina [510688] 0 Right bundle branch block http://purl.obolibrary.org/obo/HP_0011712 GCST90080006 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had cataract surgery - Right eye only (UKB data field 5324) (Gene-based burden) 588 European ancestry cases, 8,112 European ancestry controls NA Illumina [72009] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90083327 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I47.2: Ventricular tachycardia 1,144 European ancestry cases, 386,786 European ancestry controls NA Affymetrix, Illumina [510688] 0 ventricular tachycardia http://www.ebi.ac.uk/efo/EFO_0005306 GCST90080012 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had cervical smear test (UKB data field 2694) (Gene-based burden) 228,394 European ancestry cases, 4,737 European ancestry controls NA Illumina [181152] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90082942 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I48.0: Paroxysmal atrial fibrillation 1,162 European ancestry cases, 386,768 European ancestry controls NA Affymetrix, Illumina [510688] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90080014 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had hysterectomy - womb removed (UKB data field 3591) (Gene-based burden) 18,107 European ancestry cases, 188,986 European ancestry controls NA Illumina [179573] 0 hysterectomy http://www.ebi.ac.uk/efo/EFO_0003881 GCST90083051 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.4: Non-ST elevation (NSTEMI) myocardial infarction 1,862 European ancestry cases, 386,068 European ancestry controls NA Affymetrix, Illumina [510688] 0 Non-ST Elevation Myocardial Infarction http://www.ebi.ac.uk/efo/EFO_0008586 GCST90079971 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever believed in unreal communications or signs (UKB data field 20474) (Gene-based burden) 982 European ancestry cases, 138,332 European ancestry controls NA Illumina [172090] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082494 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I24.8: Other forms of acute ischemic heart disease 749 European ancestry cases, 387,181 European ancestry controls NA Affymetrix, Illumina [510688] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90079975 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever contemplated self harm more than once (UKB data field 20485) (Gene-based burden) 10,186 European ancestry cases, 128,964 European ancestry controls NA Illumina [172047] 0 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST90082505 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.2: Old myocardial infarction 10,313 European ancestry cases, 377,617 European ancestry controls NA Affymetrix, Illumina [510688] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90079979 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever contemplated self harm once (UKB data field 20485) (Gene-based burden) 10,426 European ancestry cases, 128,724 European ancestry controls NA Illumina [172047] 0 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST90082504 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I27.0: Primary pulmonary hypertension 525 European ancestry cases, 387,405 European ancestry controls NA Affymetrix, Illumina [510688] 0 primary pulmonary hypertension http://purl.obolibrary.org/obo/MONDO_0001999 GCST90079985 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever depressed for a whole week (UKB data field 4598) (Gene-based burden) 94,987 European ancestry cases, 79,419 European ancestry controls NA Illumina [176845] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90083197 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I34.1: Nonrheumatic mitral (valve) prolapse 694 European ancestry cases, 387,236 European ancestry controls NA Affymetrix, Illumina [510688] 0 Mitral valve prolapse http://purl.obolibrary.org/obo/HP_0001634 GCST90079992 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever felt worried tense or anxious for most of a month or longer (UKB data field 20421) (Gene-based burden) 34,789 European ancestry cases, 95,747 European ancestry controls NA Illumina [170556] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082425 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 500 Never (UKB data field 21033) (Gene-based burden) 73,989 European ancestry cases, 81,088 European ancestry controls NA Illumina [174046] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082708 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.1: Alcohol use 10,125 European ancestry cases, 377,805 European ancestry controls NA Affymetrix, Illumina [510688] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081311 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 501 Sometimes (UKB data field 21033) (Gene-based burden) 61,495 European ancestry cases, 93,582 European ancestry controls NA Illumina [174046] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082709 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.1: Personal history of malignant neoplasm of trachea, bronchus and lung 884 European ancestry cases, 387,044 European ancestry controls NA Affymetrix, Illumina [510688] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90081348 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 502 Often (UKB data field 21033) (Gene-based burden) 12,932 European ancestry cases, 142,145 European ancestry controls NA Illumina [174046] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082710 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.7: Personal history of other malignant neoplasms of lymphoid, hematopoietic and related tissues 1,462 European ancestry cases, 386,468 European ancestry controls NA Affymetrix, Illumina [510688] 0 GCST90081352 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 503 Most of the time (UKB data field 21033) (Gene-based burden) 5,881 European ancestry cases, 149,196 European ancestry controls NA Illumina [174046] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082711 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.4: Personal history of psychoactive substance abuse 39,220 European ancestry cases, 348,710 European ancestry controls NA Affymetrix, Illumina [510688] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081359 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 504 Always (UKB data field 21033) (Gene-based burden) 780 European ancestry cases, 154,297 European ancestry controls NA Illumina [174046] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082712 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.5: Allergy status to narcotic agent status 1,709 European ancestry cases, 386,221 European ancestry controls NA Affymetrix, Illumina [510688] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081384 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 500 Never (UKB data field 21032) (Gene-based burden) 41,782 European ancestry cases, 41,364 European ancestry controls NA Illumina [159641] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082703 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.6: Personal history of other physical trauma 726 European ancestry cases, 387,204 European ancestry controls NA Affymetrix, Illumina [510688] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081400 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E55: Vitamin D deficiency (Gene-based burden) 1,437 European ancestry cases, 383,546 European ancestry controls NA Illumina [185279] 0 vitamin D deficiency http://www.ebi.ac.uk/efo/EFO_0003762 GCST90083746 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I74: Arterial embolism and thrombosis 1,162 European ancestry cases, 386,633 European ancestry controls NA Affymetrix, Illumina [510544] 0 arterial embolism, Arterial thrombosis http://www.ebi.ac.uk/efo/EFO_0010671, http://purl.obolibrary.org/obo/HP_0004420 GCST90080053 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E55.9: Vitamin D deficiency, unspecified (Gene-based burden) 1,372 European ancestry cases, 384,186 European ancestry controls NA Illumina [185287] 0 vitamin D deficiency http://www.ebi.ac.uk/efo/EFO_0003762 GCST90083745 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eosinophill count (UKB data field 30150) (Gene-based burden) 418,449 European ancestry individuals NA Illumina [185795] 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90082980 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.2: Primary angle-closure glaucoma 926 European ancestry cases, 387,004 European ancestry controls NA Affymetrix, Illumina [510688] 0 primary angle closure glaucoma http://www.ebi.ac.uk/efo/EFO_1001506 GCST90079907 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eosinophill percentage (UKB data field 30210) (Gene-based burden) 418,454 European ancestry individuals NA Illumina [185795] 0 eosinophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007991 GCST90082984 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.9: Unspecified glaucoma 3,672 European ancestry cases, 384,258 European ancestry controls 2,290 European ancestry cases, 113,883 European ancestry controls Affymetrix, Illumina [510688] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90079908 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to a behaviour or miscellanous (UKB data field 20431) (Gene-based burden) 1,959 European ancestry cases, 6,226 European ancestry controls NA Illumina [69082] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90082433 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H52.1: Myopia 1,781 European ancestry cases, 386,149 European ancestry controls NA Affymetrix, Illumina [510688] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90079916 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to alcohol (UKB data field 20406) (Gene-based burden) 3,191 European ancestry cases, 4,505 European ancestry controls NA Illumina [66767] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90082391 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.2: Diplopia 923 European ancestry cases, 387,007 European ancestry controls NA Affymetrix, Illumina [510688] 0 Diplopia http://purl.obolibrary.org/obo/HP_0000651 GCST90079920 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to any substance or behaviour (UKB data field 20401) (Gene-based burden) 8,298 European ancestry cases, 129,860 European ancestry controls NA Illumina [171900] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90082382 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81.0: Meniere's disease 714 European ancestry cases, 387,216 European ancestry controls NA Affymetrix, Illumina [510688] 0 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90079942 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to illicit or recreational drugs (UKB data field 20456) (Gene-based burden) 654 European ancestry cases, 7,551 European ancestry controls NA Illumina [69253] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90082466 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H83.0: Labyrinthitis 897 European ancestry cases, 387,033 European ancestry controls NA Affymetrix, Illumina [510688] 0 labyrinthitis http://www.ebi.ac.uk/efo/EFO_0009604 GCST90079944 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to prescription or over the counter medication (UKB data field 20503) (Gene-based burden) 1,162 European ancestry cases, 7,018 European ancestry controls NA Illumina [69135] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90082544 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08.0: Rheumatic disorders of both mitral and aortic valves 732 European ancestry cases, 387,198 European ancestry controls NA Affymetrix, Illumina [510688] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90079958 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever attempted suicide (UKB data field 20483) (Gene-based burden) 3,119 European ancestry cases, 2,743 European ancestry controls NA Illumina [56886] 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90082503 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08.1: Rheumatic disorders of both mitral and tricuspid valves 1,144 European ancestry cases, 386,786 European ancestry controls NA Affymetrix, Illumina [510688] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90079959 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been injured or injured someone else through drinking alcohol but not in the last year (UKB data field 20411) (Gene-based burden) 5,296 European ancestry cases, 134,344 European ancestry controls NA Illumina [172136] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90082405 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I12.0: Hypertensive chronic kidney disease with stage 5 chronic kidney disease or end stage renal disease 1,504 European ancestry cases, 386,426 European ancestry controls 956 European ancestry cases, 107,322 European ancestry controls Affymetrix, Illumina [510688] 0 hypertensive nephropathy http://purl.obolibrary.org/obo/MONDO_0024633 GCST90079963 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been injured or injured someone else through drinking alcohol during the last year (UKB data field 20411) (Gene-based burden) 644 European ancestry cases, 138,996 European ancestry controls NA Illumina [172136] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90082406 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20.8: Other forms of angina pectoris 1,225 European ancestry cases, 386,705 European ancestry controls NA Affymetrix, Illumina [510688] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90079966 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been offered or sought treatment for anxiety (UKB data field 21062) (Gene-based burden) 34,901 European ancestry cases, 119,860 European ancestry controls NA Illumina [174020] 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90082812 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.0: ST elevation (STEMI) myocardial infarction of anterior wall 1,954 European ancestry cases, 385,976 European ancestry controls NA Affymetrix, Illumina [510688] 0 ST Elevation Myocardial Infarction http://www.ebi.ac.uk/efo/EFO_0008585 GCST90079969 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been offered or sought treatment for depression (UKB data field 21063) (Gene-based burden) 37,813 European ancestry cases, 116,887 European ancestry controls NA Illumina [174026] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082813 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.1: ST elevation (STEMI) myocardial infarction of inferior wall 2,404 European ancestry cases, 385,526 European ancestry controls NA Affymetrix, Illumina [510688] 0 ST Elevation Myocardial Infarction http://www.ebi.ac.uk/efo/EFO_0008585 GCST90079970 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever believed in an unreal conspiracy against self (UKB data field 20468) (Gene-based burden) 1,103 European ancestry cases, 138,270 European ancestry controls NA Illumina [172075] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082492 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R47.0: Dysphasia and aphasia 948 European ancestry cases, 386,838 European ancestry controls NA Affymetrix, Illumina [510543] 0 specific language disorder http://purl.obolibrary.org/obo/MONDO_0016226 GCST90080862 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E61: Deficiency of other nutrient elements (Gene-based burden) 542 European ancestry cases, 386,428 European ancestry controls NA Illumina [185322] 0 disorder of metabolite absorption and transport http://purl.obolibrary.org/obo/MONDO_0017757 GCST90083747 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G81.9: Hemiplegia, unspecified 2,024 European ancestry cases, 385,757 European ancestry controls NA Affymetrix, Illumina [510541] 0 hemiplegia http://www.ebi.ac.uk/efo/EFO_0009453 GCST90079853 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E66: Overweight and obesity (Gene-based burden) 171,670 European ancestry cases, 194,798 European ancestry controls NA Illumina [184975] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90083750 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K41: Femoral hernia 806 European ancestry cases, 386,955 European ancestry controls NA Affymetrix, Illumina [510541] 0 femoral hernia http://www.ebi.ac.uk/efo/EFO_1001791 GCST90080222 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E66.8: Other obesity (Gene-based burden) 2,009 European ancestry cases, 385,921 European ancestry controls NA Illumina [185344] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90083748 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.4: Localized swelling, mass and lump, lower limb 681 European ancestry cases, 387,076 European ancestry controls NA Affymetrix, Illumina [510538] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90080821 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E66.9: Obesity, unspecified (Gene-based burden) 170,856 European ancestry cases, 195,879 European ancestry controls NA Illumina [184979] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90083749 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D04: Carcinoma in situ of skin 973 European ancestry cases, 386,773 European ancestry controls 908 European ancestry cases, 120,817 European ancestry controls Affymetrix, Illumina [510536] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079645 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78: Disorders of lipoprotein metabolism and other lipidemias (Gene-based burden) 51,365 European ancestry cases, 320,834 European ancestry controls NA Illumina [185113] 0 Disorder of amino acid and other organic acid metabolism http://www.orpha.net/ORDO/Orphanet_79062 GCST90083754 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00.8: Superficial injury of other parts of head 1,368 European ancestry cases, 386,390 European ancestry controls NA Affymetrix, Illumina [510535] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080939 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78.0: Pure hypercholesterolemia (Gene-based burden) 45,730 European ancestry cases, 332,541 European ancestry controls NA Illumina [185194] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90083752 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.6: Other and unspecified intestinal obstruction 2,586 European ancestry cases, 385,172 European ancestry controls NA Affymetrix, Illumina [510534] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080242 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78.00: Pure hypercholesterolemia, unspecified (Gene-based burden) 5,498 European ancestry cases, 369,901 European ancestry controls NA Illumina [185148] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90083751 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.815.013.: Other complications of procedures, not elsewhere classified 2,476 European ancestry cases, 385,251 European ancestry controls NA Affymetrix, Illumina [510534] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081073 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78.5: Hyperlipidemia, unspecified (Gene-based burden) 6,517 European ancestry cases, 381,413 European ancestry controls NA Illumina [185344] 0 hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0021187 GCST90083753 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S66: Injury of muscle, fascia and tendon at wrist and hand level 1,424 European ancestry cases, 386,327 European ancestry controls NA Affymetrix, Illumina [510533] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081006 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E80: Disorders of porphyrin and bilirubin metabolism (Gene-based burden) 614 European ancestry cases, 386,552 European ancestry controls NA Illumina [185332] 0 disorder of metabolite absorption and transport http://purl.obolibrary.org/obo/MONDO_0017757 GCST90083755 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.9: Bladder disorder, unspecified 964 European ancestry cases, 386,803 European ancestry controls NA Affymetrix, Illumina [510529] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90080606 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E83: Disorders of mineral metabolism (Gene-based burden) 3,300 European ancestry cases, 383,907 European ancestry controls NA Illumina [185319] 0 mineral metabolism disease http://www.ebi.ac.uk/efo/EFO_0009556 GCST90083758 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M80: Osteoporosis with current pathological fracture 1,190 European ancestry cases, 386,550 European ancestry controls NA Affymetrix, Illumina [510527] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90080556 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E83.4: Disorders of magnesium metabolism (Gene-based burden) 684 European ancestry cases, 387,246 European ancestry controls NA Illumina [185344] 0 mineral metabolism disease http://www.ebi.ac.uk/efo/EFO_0009556 GCST90083756 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E83.5: Disorders of calcium metabolism 1,603 European ancestry cases, 386,117 European ancestry controls NA Affymetrix, Illumina [510525] 0 calcium metabolic disease http://www.ebi.ac.uk/efo/EFO_0005769 GCST90079771 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E83.5: Disorders of calcium metabolism (Gene-based burden) 1,603 European ancestry cases, 386,117 European ancestry controls NA Illumina [185343] 0 calcium metabolic disease http://www.ebi.ac.uk/efo/EFO_0005769 GCST90083757 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.9: Synovitis and tenosynovitis, unspecified 2,614 European ancestry cases, 385,133 European ancestry controls NA Affymetrix, Illumina [510524] 0 pigmented villonodular synovitis http://www.ebi.ac.uk/efo/EFO_1001106 GCST90080519 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F32: Major depressive disorder, single episode (Gene-based burden) 25,879 European ancestry cases, 346,278 European ancestry controls NA Illumina [185127] 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90083790 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K70: Alcoholic liver disease 1,120 European ancestry cases, 386,551 European ancestry controls NA Affymetrix, Illumina [510487] 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90080283 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F32.9: Major depressive disorder, single episode, unspecified (Gene-based burden) 22,358 European ancestry cases, 355,688 European ancestry controls NA Illumina [185180] 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90083789 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.8: Other specified counseling 675 European ancestry cases, 387,017 European ancestry controls NA Affymetrix, Illumina [510486] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081307 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F33: Major depressive disorder, recurrent (Gene-based burden) 1,721 European ancestry cases, 384,459 European ancestry controls NA Illumina [185299] 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90083791 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D13: Benign neoplasm of other and ill-defined parts of digestive system 1,532 European ancestry cases, 386,164 European ancestry controls 640 European ancestry cases, 101,962 European ancestry controls Affymetrix, Illumina [510485] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079664 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F40: Phobic anxiety disorders (Gene-based burden) 1,328 European ancestry cases, 384,738 European ancestry controls NA Illumina [185311] 0 phobic disorder http://www.ebi.ac.uk/efo/EFO_1001908 GCST90083793 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I35.1: Nonrheumatic aortic (valve) insufficiency 994 European ancestry cases, 386,698 European ancestry controls NA Affymetrix, Illumina [510485] 0 aortic valve insufficiency http://www.ebi.ac.uk/efo/EFO_0007148 GCST90079995 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F40.2: Specific (isolated) phobias (Gene-based burden) 804 European ancestry cases, 386,882 European ancestry controls NA Illumina [185342] 0 phobic disorder http://www.ebi.ac.uk/efo/EFO_1001908 GCST90083792 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L89: Pressure ulcer 1,643 European ancestry cases, 386,053 European ancestry controls NA Affymetrix, Illumina [510485] 0 decubitus ulcer http://www.ebi.ac.uk/efo/EFO_0007067 GCST90080374 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41: Other anxiety disorders (Gene-based burden) 17,585 European ancestry cases, 353,730 European ancestry controls NA Illumina [185063] 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90083798 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M11: Other crystal arthropathies 581 European ancestry cases, 387,116 European ancestry controls NA Affymetrix, Illumina [510485] 0 crystal arthropathy http://purl.obolibrary.org/obo/MONDO_0022208 GCST90080397 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.0: Panic disorder [episodic paroxysmal anxiety] (Gene-based burden) 1,685 European ancestry cases, 383,717 European ancestry controls NA Illumina [185309] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90083794 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N19: Unspecified kidney failure 1,792 European ancestry cases, 385,939 European ancestry controls NA Affymetrix, Illumina [510484] 0 kidney failure http://www.ebi.ac.uk/efo/EFO_1002048 GCST90080585 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.1: Generalized anxiety disorder (Gene-based burden) 2,967 European ancestry cases, 378,840 European ancestry controls NA Illumina [185231] 0 generalized anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001892 GCST90083795 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.8: Other specified diseases of anus and rectum 3,323 European ancestry cases, 384,403 European ancestry controls NA Affymetrix, Illumina [510483] 0 anus disease http://www.ebi.ac.uk/efo/EFO_0009660 GCST90080267 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.2: Mixed anxiety and depressive disorder (Gene-based burden) 2,046 European ancestry cases, 385,884 European ancestry controls NA Illumina [185344] 0 mixed anxiety and depressive disorder http://purl.obolibrary.org/obo/MONDO_0041086 GCST90083796 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Q21: Congenital malformations of cardiac septa 724 European ancestry cases, 386,970 European ancestry controls NA Affymetrix, Illumina [510483] 0 Abnormal cardiac septum morphology http://purl.obolibrary.org/obo/HP_0001671 GCST90080748 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.9: Anxiety disorder, unspecified (Gene-based burden) 9,404 European ancestry cases, 372,895 European ancestry controls NA Illumina [185265] 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90083797 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F40.2: Specific (isolated) phobias 804 European ancestry cases, 386,882 European ancestry controls NA Affymetrix, Illumina [510482] 0 phobic disorder http://www.ebi.ac.uk/efo/EFO_1001908 GCST90079806 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F43: Reaction to severe stress, and adjustment disorders (Gene-based burden) 4,612 European ancestry cases, 374,861 European ancestry controls NA Illumina [185220] 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90083799 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I42: Cardiomyopathy 1,789 European ancestry cases, 385,920 European ancestry controls 3,264 European ancestry cases, 94,883 European ancestry controls Affymetrix, Illumina [510481] 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST90080000 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F45: Somatoform disorders (Gene-based burden) 844 European ancestry cases, 384,989 European ancestry controls NA Illumina [185304] 0 somatoform disorder http://www.ebi.ac.uk/efo/EFO_0009687 GCST90083800 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L27: Dermatitis due to substances taken internally 633 European ancestry cases, 387,042 European ancestry controls NA Affymetrix, Illumina [510481] 0 dermatitis http://purl.obolibrary.org/obo/MONDO_0002406 GCST90080341 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F52: Sexual dysfunction not due to a substance or known physiological condition (Gene-based burden) 682 European ancestry cases, 385,926 European ancestry controls NA Illumina [185323] 0 physiological sexual disorder http://purl.obolibrary.org/obo/MONDO_0002134 GCST90083801 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E86: Volume depletion (Gene-based burden) 4,194 European ancestry cases, 383,606 European ancestry controls NA Illumina [185341] 0 Hypovolemia http://purl.obolibrary.org/obo/HP_0011106 GCST90083759 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.0: Amblyopia ex anopsia 794 European ancestry cases, 386,946 European ancestry controls NA Affymetrix, Illumina [510520] 0 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST90079918 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87: Other disorders of fluid, electrolyte and acid-base balance (Gene-based burden) 9,393 European ancestry cases, 375,084 European ancestry controls NA Illumina [185280] 0 Abnormality of metabolism/homeostasis http://purl.obolibrary.org/obo/HP_0001939 GCST90083765 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D61: Other aplastic anemias and other bone marrow failure syndromes 645 European ancestry cases, 387,116 European ancestry controls NA Affymetrix, Illumina [510519] 0 bone marrow failure syndrome, anemia (phenotype) http://purl.obolibrary.org/obo/MONDO_0000159, http://www.ebi.ac.uk/efo/EFO_0004272 GCST90079708 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.1: Hypo-osmolality and hyponatremia (Gene-based burden) 3,625 European ancestry cases, 382,688 European ancestry controls NA Illumina [185316] 0 Abnormality of metabolism/homeostasis http://purl.obolibrary.org/obo/HP_0001939 GCST90083760 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.5: Hyperkalemia 1,532 European ancestry cases, 386,194 European ancestry controls NA Affymetrix, Illumina [510519] 0 Hyperkalemia http://purl.obolibrary.org/obo/HP_0002153 GCST90079776 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.2: Acidosis (Gene-based burden) 1,660 European ancestry cases, 386,169 European ancestry controls NA Illumina [185331] 0 acidosis http://www.ebi.ac.uk/efo/EFO_1000014 GCST90083761 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F03: Unspecified dementia 1,165 European ancestry cases, 386,569 European ancestry controls NA Affymetrix, Illumina [510519] 0 dementia http://purl.obolibrary.org/obo/MONDO_0001627 GCST90079784 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.5: Hyperkalemia (Gene-based burden) 1,532 European ancestry cases, 386,194 European ancestry controls NA Illumina [185341] 0 Hyperkalemia http://purl.obolibrary.org/obo/HP_0002153 GCST90083762 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K13.7: Other and unspecified lesions of oral mucosa 2,223 European ancestry cases, 385,531 European ancestry controls NA Affymetrix, Illumina [510518] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90080181 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.6: Hypokalemia (Gene-based burden) 2,299 European ancestry cases, 385,620 European ancestry controls NA Illumina [185344] 0 Hypokalemia http://purl.obolibrary.org/obo/HP_0002900 GCST90083763 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.3: Fracture of lower end of tibia 648 European ancestry cases, 387,110 European ancestry controls NA Affymetrix, Illumina [510518] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90081021 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.7: Fluid overload (Gene-based burden) 804 European ancestry cases, 387,126 European ancestry controls NA Illumina [185344] 0 Hypervolemia http://purl.obolibrary.org/obo/HP_0011105 GCST90083764 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.2: Precordial pain 4,782 European ancestry cases, 382,966 European ancestry controls NA Affymetrix, Illumina [510517] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90080773 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E88: Other and unspecified metabolic disorders (Gene-based burden) 580 European ancestry cases, 387,006 European ancestry controls NA Illumina [185338] 0 metabolic disease http://www.ebi.ac.uk/efo/EFO_0000589 GCST90083766 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E14: Unspecified diabetes mellitus 3,469 European ancestry cases, 384,252 European ancestry controls NA Affymetrix, Illumina [510516] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90079748 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E89: Postprocedural endocrine and metabolic complications and disorders, not elsewhere classified (Gene-based burden) 1,804 European ancestry cases, 385,989 European ancestry controls NA Illumina [185337] 0 metabolic disease http://www.ebi.ac.uk/efo/EFO_0000589 GCST90083768 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F31: Bipolar disorder 1,355 European ancestry cases, 386,380 European ancestry controls NA Affymetrix, Illumina [510513] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90079802 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E89.0: Postprocedural hypothyroidism (Gene-based burden) 1,439 European ancestry cases, 386,491 European ancestry controls NA Illumina [185344] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90083767 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T40.2: Poisoning by, adverse effect of and underdosing of other opioids 636 European ancestry cases, 387,063 European ancestry controls NA Affymetrix, Illumina [510512] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081051 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F00: Dementia in Alzheimer's disease (Gene-based burden) 508 European ancestry cases, 387,422 European ancestry controls NA Illumina [185301] 0 dementia http://purl.obolibrary.org/obo/MONDO_0001627 GCST90083769 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50.0: Iron deficiency anemia secondary to blood loss (chronic) 600 European ancestry cases, 387,139 European ancestry controls NA Affymetrix, Illumina [510509] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90079701 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F03: Unspecified dementia (Gene-based burden) 1,165 European ancestry cases, 386,569 European ancestry controls NA Illumina [185340] 0 dementia http://purl.obolibrary.org/obo/MONDO_0001627 GCST90083770 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K65: Peritonitis 1,102 European ancestry cases, 386,626 European ancestry controls NA Affymetrix, Illumina [510509] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90080279 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F05: Delirium due to known physiological condition (Gene-based burden) 1,350 European ancestry cases, 386,554 European ancestry controls NA Illumina [185344] 0 alcohol withdrawal delirium http://www.ebi.ac.uk/efo/EFO_1000800 GCST90083772 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J35: Chronic diseases of tonsils and adenoids 1,191 European ancestry cases, 385,993 European ancestry controls NA Affymetrix, Illumina [510010] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080118 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I34: Nonrheumatic mitral valve disorders (Gene-based burden) 3,369 European ancestry cases, 383,491 European ancestry controls NA Illumina [185334] 0 mitral valve disease http://www.ebi.ac.uk/efo/EFO_0009557 GCST90083979 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M24: Other specific joint derangements 3,202 European ancestry cases, 383,964 European ancestry controls NA Affymetrix, Illumina [510008] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90080450 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I34.0: Nonrheumatic mitral (valve) insufficiency (Gene-based burden) 2,987 European ancestry cases, 384,345 European ancestry controls NA Illumina [185337] 0 mitral valve disease http://www.ebi.ac.uk/efo/EFO_0009557 GCST90083977 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M86: Osteomyelitis 763 European ancestry cases, 386,454 European ancestry controls NA Affymetrix, Illumina [510008] 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90080564 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I34.1: Nonrheumatic mitral (valve) prolapse (Gene-based burden) 694 European ancestry cases, 387,236 European ancestry controls NA Illumina [185344] 0 Mitral valve prolapse http://purl.obolibrary.org/obo/HP_0001634 GCST90083978 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S86.0: Injury of Achilles tendon 825 European ancestry cases, 386,304 European ancestry controls NA Affymetrix, Illumina [510007] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081032 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I35: Nonrheumatic aortic valve disorders (Gene-based burden) 3,782 European ancestry cases, 383,293 European ancestry controls NA Illumina [185334] 0 aortic valve disease http://www.ebi.ac.uk/efo/EFO_0009531 GCST90083982 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z75.1: Person awaiting admission to adequate facility elsewhere 988 European ancestry cases, 386,207 European ancestry controls NA Affymetrix, Illumina [510005] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081320 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I35.0: Nonrheumatic aortic (valve) stenosis (Gene-based burden) 2,514 European ancestry cases, 385,181 European ancestry controls NA Illumina [185340] 0 aortic stenosis http://www.ebi.ac.uk/efo/EFO_0000266 GCST90083980 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E10: Type 1 diabetes mellitus 3,971 European ancestry cases, 383,232 European ancestry controls NA Affymetrix, Illumina [509995] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90079733 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I35.1: Nonrheumatic aortic (valve) insufficiency (Gene-based burden) 994 European ancestry cases, 386,698 European ancestry controls NA Illumina [185342] 0 aortic valve insufficiency http://www.ebi.ac.uk/efo/EFO_0007148 GCST90083981 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K61: Abscess of anal and rectal regions 1,733 European ancestry cases, 385,413 European ancestry controls NA Affymetrix, Illumina [509993] 0 Rectal abscess http://purl.obolibrary.org/obo/HP_0005224 GCST90080261 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I38: Endocarditis, valve unspecified (Gene-based burden) 572 European ancestry cases, 387,181 European ancestry controls NA Illumina [185343] 0 endocarditis http://www.ebi.ac.uk/efo/EFO_0000465 GCST90083983 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I63: Cerebral infarction 4,520 European ancestry cases, 382,615 European ancestry controls NA Affymetrix, Illumina [509984] 0 brain infarction http://www.ebi.ac.uk/efo/EFO_0004277 GCST90080035 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I42: Cardiomyopathy (Gene-based burden) 1,789 European ancestry cases, 385,920 European ancestry controls NA Illumina [185339] 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST90083986 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63.0: Anorexia 1,199 European ancestry cases, 385,979 European ancestry controls NA Affymetrix, Illumina [509983] 0 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST90080893 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I42.0: Dilated cardiomyopathy (Gene-based burden) 858 European ancestry cases, 387,072 European ancestry controls NA Illumina [185344] 0 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST90083984 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25: Chronic ischemic heart disease 32,706 European ancestry cases, 354,404 European ancestry controls 22,632 European ancestry cases, 96,213 European ancestry controls Affymetrix, Illumina [509982] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90079982 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I42.9: Cardiomyopathy, unspecified (Gene-based burden) 681 European ancestry cases, 387,249 European ancestry controls NA Illumina [185344] 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST90083985 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L85.3: Xerosis cutis (Gene-based burden) 964 European ancestry cases, 381,055 European ancestry controls NA Illumina [185253] 0 Dry skin http://purl.obolibrary.org/obo/HP_0000958 GCST90084357 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M43: Other deforming dorsopathies 2,743 European ancestry cases, 381,483 European ancestry controls NA Affymetrix, Illumina [507402] 0 skeletal system disease http://www.ebi.ac.uk/efo/EFO_0002461 GCST90080475 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L89: Pressure ulcer (Gene-based burden) 1,643 European ancestry cases, 386,053 European ancestry controls NA Illumina [185340] 0 decubitus ulcer http://www.ebi.ac.uk/efo/EFO_0007067 GCST90084360 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81: Osteoporosis without current pathological fracture 10,456 European ancestry cases, 373,627 European ancestry controls NA Affymetrix, Illumina [507399] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90080559 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L89.1: Pressure ulcer of back (Gene-based burden) 604 European ancestry cases, 387,326 European ancestry controls NA Illumina [185344] 0 chronic ulcer of skin http://www.ebi.ac.uk/efo/EFO_0007066 GCST90084359 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50.9: Heart failure, unspecified (Gene-based burden) 2,407 European ancestry cases, 385,523 European ancestry controls NA Illumina [185344] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90084008 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.0: Localized swelling, mass and lump, head 528 European ancestry cases, 386,502 European ancestry controls NA Affymetrix, Illumina [509922] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90080819 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51: Complications and ill-defined descriptions of heart disease (Gene-based burden) 6,712 European ancestry cases, 379,168 European ancestry controls NA Illumina [185305] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90084013 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K43: Ventral hernia 4,359 European ancestry cases, 382,701 European ancestry controls NA Affymetrix, Illumina [509918] 0 ventral hernia http://www.ebi.ac.uk/efo/EFO_1001866 GCST90080226 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51.7: Cardiomegaly (Gene-based burden) 3,998 European ancestry cases, 383,170 European ancestry controls NA Illumina [185332] 0 cardiac hypertrophy http://www.ebi.ac.uk/efo/EFO_0002503 GCST90084010 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S43.0: Subluxation and dislocation of shoulder joint 584 European ancestry cases, 386,546 European ancestry controls NA Affymetrix, Illumina [509918] 0 dislocation, sprain http://www.ebi.ac.uk/efo/EFO_0009521, http://www.ebi.ac.uk/efo/EFO_0009582 GCST90080981 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51.8: Other ill-defined heart diseases (Gene-based burden) 2,078 European ancestry cases, 385,851 European ancestry controls NA Illumina [185344] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90084011 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart failure 8,159 European ancestry cases, 378,891 European ancestry controls NA Affymetrix, Illumina [509904] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90081485 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51.9: Heart disease, unspecified (Gene-based burden) 909 European ancestry cases, 386,964 European ancestry controls NA Illumina [185343] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90084012 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.6: Fracture of lower end of ulna 1,019 European ancestry cases, 385,988 European ancestry controls NA Affymetrix, Illumina [509904] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080990 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I60: Nontraumatic subarachnoid hemorrhage (Gene-based burden) 1,067 European ancestry cases, 386,623 European ancestry controls NA Illumina [185341] 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90084015 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05.9: Thyrotoxicosis, unspecified 2,203 European ancestry cases, 384,824 European ancestry controls NA Affymetrix, Illumina [509895] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90079729 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I60.9: Nontraumatic subarachnoid hemorrhage, unspecified (Gene-based burden) 701 European ancestry cases, 387,022 European ancestry controls NA Illumina [185337] 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90084014 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z60: Problems related to social environment 4,391 European ancestry cases, 382,712 European ancestry controls NA Affymetrix, Illumina [509893] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081299 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I61: Nontraumatic intracerebral hemorrhage (Gene-based burden) 1,085 European ancestry cases, 386,689 European ancestry controls NA Illumina [185339] 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90084017 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K10: Other diseases of jaws 537 European ancestry cases, 386,441 European ancestry controls NA Affymetrix, Illumina [509892] 0 jaw disease http://www.ebi.ac.uk/efo/EFO_0009468 GCST90080176 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I61.9: Nontraumatic intracerebral hemorrhage, unspecified (Gene-based burden) 698 European ancestry cases, 387,165 European ancestry controls NA Illumina [185343] 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90084016 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40.9: Psoriasis, unspecified 2,364 European ancestry cases, 384,617 European ancestry controls 1,871 European ancestry cases, 118,929 European ancestry controls Affymetrix, Illumina [509892] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90080348 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I62: Other and unspecified nontraumatic intracranial hemorrhage (Gene-based burden) 590 European ancestry cases, 387,284 European ancestry controls NA Illumina [185343] 0 intracranial hemorrhage http://www.ebi.ac.uk/efo/EFO_0000551 GCST90084018 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00.9: Superficial injury of unspecified part of head 714 European ancestry cases, 386,310 European ancestry controls NA Affymetrix, Illumina [509888] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080940 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I63: Cerebral infarction (Gene-based burden) 4,520 European ancestry cases, 382,615 European ancestry controls NA Illumina [185334] 0 brain infarction http://www.ebi.ac.uk/efo/EFO_0004277 GCST90084021 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coronary artery disease - loose 33,971 European ancestry cases, 353,040 European ancestry controls NA Affymetrix, Illumina [509887] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90081465 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I63.5: Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries (Gene-based burden) 552 European ancestry cases, 387,378 European ancestry controls NA Illumina [185344] 0 cerebral infarction http://purl.obolibrary.org/obo/MONDO_0002679 GCST90084019 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I89: Other noninfective disorders of lymphatic vessels and lymph nodes 1,174 European ancestry cases, 385,860 European ancestry controls NA Affymetrix, Illumina [509886] 0 lymphatic system disease http://www.ebi.ac.uk/efo/EFO_0007352 GCST90080080 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I63.9: Cerebral infarction, unspecified (Gene-based burden) 3,386 European ancestry cases, 384,117 European ancestry controls NA Illumina [185337] 0 cerebral infarction http://purl.obolibrary.org/obo/MONDO_0002679 GCST90084020 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25: Chronic ischemic heart disease (Gene-based burden) 32,706 European ancestry cases, 354,404 European ancestry controls NA Illumina [185334] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90083968 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K25: Gastric ulcer 5,549 European ancestry cases, 381,689 European ancestry controls NA Affymetrix, Illumina [510049] 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90080197 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.1: Atherosclerotic heart disease of native coronary artery (Gene-based burden) 23,129 European ancestry cases, 364,782 European ancestry controls NA Illumina [185343] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90083964 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72: Fracture of femur 3,054 European ancestry cases, 384,117 European ancestry controls NA Affymetrix, Illumina [510045] 0 femur fracture http://www.ebi.ac.uk/efo/EFO_0008553 GCST90081013 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.2: Old myocardial infarction (Gene-based burden) 10,313 European ancestry cases, 377,617 European ancestry controls NA Illumina [185344] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90083965 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R15: Fecal incontinence 2,597 European ancestry cases, 384,604 European ancestry controls NA Affymetrix, Illumina [510043] 0 fecal incontinence http://www.ebi.ac.uk/efo/EFO_0009523 GCST90080803 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.8: Other forms of chronic ischemic heart disease (Gene-based burden) 7,721 European ancestry cases, 380,198 European ancestry controls NA Illumina [185344] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90083966 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M89: Other disorders of bone 1,953 European ancestry cases, 385,201 European ancestry controls NA Affymetrix, Illumina [510040] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90080567 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.9: Chronic ischemic heart disease, unspecified (Gene-based burden) 17,106 European ancestry cases, 369,135 European ancestry controls NA Illumina [185315] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90083967 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.2: Fracture of shaft of tibia 684 European ancestry cases, 386,536 European ancestry controls NA Affymetrix, Illumina [510037] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90081020 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I26: Pulmonary embolism (Gene-based burden) 5,221 European ancestry cases, 381,985 European ancestry controls NA Illumina [185327] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90083970 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E80: Disorders of porphyrin and bilirubin metabolism 614 European ancestry cases, 386,552 European ancestry controls 518 European ancestry cases, 85,580 European ancestry controls Affymetrix, Illumina [510034] 0 disorder of metabolite absorption and transport http://purl.obolibrary.org/obo/MONDO_0017757 GCST90079769 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I26.9: Pulmonary embolism without acute cor pulmonale (Gene-based burden) 5,096 European ancestry cases, 382,414 European ancestry controls NA Illumina [185330] 0 cor pulmonale http://purl.obolibrary.org/obo/MONDO_0004596 GCST90083969 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R26.8: Other abnormalities of gait and mobility 2,708 European ancestry cases, 384,407 European ancestry controls NA Affymetrix, Illumina [510034] 0 Gait disturbance http://purl.obolibrary.org/obo/HP_0001288 GCST90080829 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I27: Other pulmonary heart diseases (Gene-based burden) 1,249 European ancestry cases, 386,560 European ancestry controls NA Illumina [185341] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90083973 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H34: Retinal vascular occlusions 972 European ancestry cases, 386,217 European ancestry controls NA Affymetrix, Illumina [510030] 0 retinal vein occlusion http://www.ebi.ac.uk/efo/EFO_1001157 GCST90079899 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I27.0: Primary pulmonary hypertension (Gene-based burden) 525 European ancestry cases, 387,405 European ancestry controls NA Illumina [185344] 0 primary pulmonary hypertension http://purl.obolibrary.org/obo/MONDO_0001999 GCST90083971 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51.7: Cardiomegaly 3,998 European ancestry cases, 383,170 European ancestry controls NA Affymetrix, Illumina [510030] 0 cardiac hypertrophy http://www.ebi.ac.uk/efo/EFO_0002503 GCST90080024 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I27.2: Other secondary pulmonary hypertension (Gene-based burden) 649 European ancestry cases, 387,279 European ancestry controls NA Illumina [185344] 0 secondary hypertension http://www.ebi.ac.uk/efo/EFO_1002034 GCST90083972 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I26: Pulmonary embolism 5,221 European ancestry cases, 381,985 European ancestry controls 3,467 European ancestry cases, 117,976 European ancestry controls Affymetrix, Illumina [510027] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90079984 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I31: Other diseases of pericardium (Gene-based burden) 1,596 European ancestry cases, 386,216 European ancestry controls NA Illumina [185341] 0 pericarditis http://www.ebi.ac.uk/efo/EFO_0007427 GCST90083976 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M85.8: Other specified disorders of bone density and structure 1,471 European ancestry cases, 385,681 European ancestry controls NA Affymetrix, Illumina [510024] 0 Abnormality of bone mineral density http://purl.obolibrary.org/obo/HP_0004348 GCST90080562 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I31.3: Pericardial effusion (noninflammatory) (Gene-based burden) 937 European ancestry cases, 386,964 European ancestry controls NA Illumina [185344] 0 pericardial effusion http://purl.obolibrary.org/obo/MONDO_0001370 GCST90083974 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H47: Other disorders of optic [2nd] nerve and visual pathways 511 European ancestry cases, 386,640 European ancestry controls NA Affymetrix, Illumina [510015] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079914 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I31.9: Disease of pericardium, unspecified (Gene-based burden) 578 European ancestry cases, 387,309 European ancestry controls NA Illumina [185344] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90083975 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30.9: Allergic rhinitis, unspecified 715 European ancestry cases, 383,607 European ancestry controls NA Affymetrix, Illumina [507395] 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90080103 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L90: Atrophic disorders of skin (Gene-based burden) 3,987 European ancestry cases, 382,110 European ancestry controls NA Illumina [185321] 0 skin atrophy http://www.ebi.ac.uk/efo/EFO_1000766 GCST90084363 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50.905.: Adverse effect of unspecified drugs, medicaments and biological substances 682 European ancestry cases, 383,434 European ancestry controls NA Affymetrix, Illumina [507394] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081058 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L90.0: Lichen sclerosus et atrophicus (Gene-based burden) 555 European ancestry cases, 387,375 European ancestry controls NA Illumina [185344] 0 lichen sclerosus et atrophicus http://purl.obolibrary.org/obo/MONDO_0007899 GCST90084361 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50.89: Other specified disorders of the male genital organs 585 European ancestry cases, 385,274 European ancestry controls NA Affymetrix, Illumina [507370] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90080633 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L90.5: Scar conditions and fibrosis of skin (Gene-based burden) 2,723 European ancestry cases, 385,128 European ancestry controls NA Illumina [185342] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084362 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R25.2: Cramp and spasm 1,279 European ancestry cases, 382,797 European ancestry controls NA Affymetrix, Illumina [507369] 0 muscle cramp http://www.ebi.ac.uk/efo/EFO_0009846 GCST90080827 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L91: Hypertrophic disorders of skin (Gene-based burden) 3,255 European ancestry cases, 376,796 European ancestry controls NA Illumina [185195] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084365 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97: Presence of other devices 3,870 European ancestry cases, 380,268 European ancestry controls NA Affymetrix, Illumina [507318] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081434 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L91.8: Other hypertrophic disorders of the skin (Gene-based burden) 1,196 European ancestry cases, 385,192 European ancestry controls NA Illumina [185330] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084364 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.3: Lack of physical exercise 867 European ancestry cases, 383,244 European ancestry controls NA Affymetrix, Illumina [507305] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081312 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L92: Granulomatous disorders of skin and subcutaneous tissue (Gene-based burden) 825 European ancestry cases, 386,387 European ancestry controls NA Illumina [185327] 0 granulomatous dermatitis http://www.ebi.ac.uk/efo/EFO_1000705 GCST90084366 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.14: Patient's other noncompliance with medication regimen 736 European ancestry cases, 383,296 European ancestry controls NA Affymetrix, Illumina [507300] 0 medication adherence behavior http://www.ebi.ac.uk/efo/EFO_0006344 GCST90081397 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L97: Non-pressure chronic ulcer of lower limb, not elsewhere classified (Gene-based burden) 1,708 European ancestry cases, 385,756 European ancestry controls NA Illumina [185340] 0 ulcer of lower limb http://www.ebi.ac.uk/efo/EFO_0007068 GCST90084367 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60: Fissure and fistula of anal and rectal regions 4,446 European ancestry cases, 379,680 European ancestry controls NA Affymetrix, Illumina [507268] 0 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90080259 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L98: Other disorders of skin and subcutaneous tissue, not elsewhere classified (Gene-based burden) 18,698 European ancestry cases, 342,663 European ancestry controls NA Illumina [184875] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084370 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.09: Other forms of dyspnea 4,927 European ancestry cases, 378,978 European ancestry controls NA Affymetrix, Illumina [507260] 0 Dyspnea http://purl.obolibrary.org/obo/HP_0002094 GCST90080766 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L98.8: Other specified disorders of the skin and subcutaneous tissue (Gene-based burden) 1,157 European ancestry cases, 386,212 European ancestry controls NA Illumina [185336] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084368 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.79: Personal history of other diseases of the circulatory system 1,822 European ancestry cases, 382,036 European ancestry controls NA Affymetrix, Illumina [507259] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90081363 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L98.9: Disorder of the skin and subcutaneous tissue, unspecified (Gene-based burden) 5,937 European ancestry cases, 377,141 European ancestry controls NA Illumina [185259] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084369 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.1: Myalgia 1,350 European ancestry cases, 382,684 European ancestry controls NA Affymetrix, Illumina [507247] 0 Myalgia http://purl.obolibrary.org/obo/HP_0003326 GCST90080544 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M00: Pyogenic arthritis (Gene-based burden) 508 European ancestry cases, 387,264 European ancestry controls NA Illumina [185343] 0 infectious arthritis http://www.ebi.ac.uk/efo/EFO_1001351 GCST90084371 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H60.9: Unspecified otitis externa 1,675 European ancestry cases, 382,290 European ancestry controls NA Affymetrix, Illumina [507246] 0 otitis externa http://www.ebi.ac.uk/efo/EFO_0009560 GCST90079928 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M05: Rheumatoid arthritis with rheumatoid factor (Gene-based burden) 769 European ancestry cases, 387,034 European ancestry controls NA Illumina [185344] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90084373 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H60.90: Unspecified otitis externa, unspecified ear 1,369 European ancestry cases, 382,576 European ancestry controls NA Affymetrix, Illumina [507233] 0 otitis externa http://www.ebi.ac.uk/efo/EFO_0009560 GCST90079927 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.2: Alcohol dependence 2,395 European ancestry cases, 384,707 European ancestry controls NA Affymetrix, Illumina [509967] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90079790 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I47: Paroxysmal tachycardia (Gene-based burden) 4,268 European ancestry cases, 382,792 European ancestry controls NA Illumina [185334] 0 paroxysmal tachycardia http://www.ebi.ac.uk/efo/EFO_0009493 GCST90083999 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D72: Other disorders of white blood cells 691 European ancestry cases, 386,364 European ancestry controls NA Affymetrix, Illumina [509964] 0 leukocyte disorder http://purl.obolibrary.org/obo/MONDO_0004805 GCST90079717 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I47.1: Supraventricular tachycardia (Gene-based burden) 2,953 European ancestry cases, 384,965 European ancestry controls NA Illumina [185344] 0 Supraventricular tachycardia http://purl.obolibrary.org/obo/HP_0004755 GCST90083997 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K05: Gingivitis and periodontal diseases 1,081 European ancestry cases, 386,036 European ancestry controls NA Affymetrix, Illumina [509962] 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90080170 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I47.2: Ventricular tachycardia (Gene-based burden) 1,144 European ancestry cases, 386,786 European ancestry controls NA Illumina [185344] 0 ventricular tachycardia http://www.ebi.ac.uk/efo/EFO_0005306 GCST90083998 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD M45: Ankylosing spondylitis 848 European ancestry cases, 386,233 European ancestry controls NA Affymetrix, Illumina [509953] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90079536 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I48: Atrial fibrillation and flutter (Gene-based burden) 20,107 European ancestry cases, 366,749 European ancestry controls NA Illumina [185322] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90084001 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L57.0: Actinic keratosis 3,010 European ancestry cases, 384,062 European ancestry controls NA Affymetrix, Illumina [509946] 0 actinic keratosis http://www.ebi.ac.uk/efo/EFO_0002496 GCST90080354 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I48.0: Paroxysmal atrial fibrillation (Gene-based burden) 1,162 European ancestry cases, 386,768 European ancestry controls NA Illumina [185344] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90084000 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D64.9: Anemia, unspecified 14,923 European ancestry cases, 372,152 European ancestry controls 23,812 European ancestry cases, 87,619 European ancestry controls Affymetrix, Illumina [509942] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90079711 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49: Other cardiac arrhythmias (Gene-based burden) 4,054 European ancestry cases, 381,711 European ancestry controls NA Illumina [185317] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90084005 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I47: Paroxysmal tachycardia 4,268 European ancestry cases, 382,792 European ancestry controls 4,745 European ancestry cases, 94,392 European ancestry controls Affymetrix, Illumina [509937] 0 paroxysmal tachycardia http://www.ebi.ac.uk/efo/EFO_0009493 GCST90080013 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49.3: Ventricular premature depolarization (Gene-based burden) 630 European ancestry cases, 387,300 European ancestry controls NA Illumina [185344] 0 ventricular ectopy http://www.ebi.ac.uk/efo/EFO_0009276 GCST90084002 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S81: Open wound of knee and lower leg 894 European ancestry cases, 386,190 European ancestry controls NA Affymetrix, Illumina [509937] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081017 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49.5: Sick sinus syndrome (Gene-based burden) 612 European ancestry cases, 387,318 European ancestry controls NA Illumina [185344] 0 sick sinus syndrome http://purl.obolibrary.org/obo/MONDO_0001823 GCST90084003 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50: Heart failure 8,159 European ancestry cases, 378,917 European ancestry controls 11,066 European ancestry cases, 93,841 European ancestry controls Affymetrix, Illumina [509933] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90080023 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49.9: Cardiac arrhythmia, unspecified (Gene-based burden) 1,299 European ancestry cases, 386,472 European ancestry controls NA Illumina [185340] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90084004 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D70: Neutropenia 4,407 European ancestry cases, 382,668 European ancestry controls 1,806 European ancestry cases, 114,388 European ancestry controls Affymetrix, Illumina [509932] 0 neutropenia http://purl.obolibrary.org/obo/MONDO_0001475 GCST90079716 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50: Heart failure (Gene-based burden) 8,159 European ancestry cases, 378,917 European ancestry controls NA Illumina [185336] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90084009 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T39.3: Poisoning by, adverse effect of and underdosing of other nonsteroidal anti-inflammatory drugs [NSAID] 517 European ancestry cases, 386,541 European ancestry controls NA Affymetrix, Illumina [509930] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081049 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50.0: Congestive heart failure (Gene-based burden) 3,182 European ancestry cases, 384,748 European ancestry controls NA Illumina [185344] 0 congestive heart failure http://www.ebi.ac.uk/efo/EFO_0000373 GCST90084006 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32: Fracture of lumbar spine and pelvis 1,842 European ancestry cases, 385,220 European ancestry controls NA Affymetrix, Illumina [509923] 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90080970 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I50.1: Left ventricular failure, unspecified (Gene-based burden) 4,762 European ancestry cases, 382,963 European ancestry controls NA Illumina [185342] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90084007 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M41: Scoliosis 1,582 European ancestry cases, 385,435 European ancestry controls NA Affymetrix, Illumina [509922] 0 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST90080472 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09: Other symptoms and signs involving the circulatory and respiratory system (Gene-based burden) 5,437 European ancestry cases, 369,196 European ancestry controls NA Illumina [185103] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90084770 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Atopy 46,691 European ancestry cases, 313,235 European ancestry controls NA Affymetrix, Illumina [485597] 1 atopy http://www.ebi.ac.uk/efo/EFO_0002686 GCST90081463 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.1: Pleurisy (Gene-based burden) 798 European ancestry cases, 385,742 European ancestry controls NA Illumina [185305] 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90084766 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.9: Counseling, unspecified 46,702 European ancestry cases, 313,285 European ancestry controls NA Affymetrix, Illumina [485473] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081308 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.3: Abnormal sputum (Gene-based burden) 578 European ancestry cases, 385,258 European ancestry controls NA Illumina [185302] 0 Abnormal sputum http://purl.obolibrary.org/obo/HP_0032016 GCST90084767 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.1: Fracture of upper end of radius 529 European ancestry cases, 386,599 European ancestry controls NA Affymetrix, Illumina [509982] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080986 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44: Atrioventricular and left bundle-branch block (Gene-based burden) 5,320 European ancestry cases, 382,051 European ancestry controls NA Illumina [185332] 0 bundle branch block http://www.ebi.ac.uk/efo/EFO_0004138 GCST90083991 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I67: Other cerebrovascular diseases 3,818 European ancestry cases, 383,266 European ancestry controls NA Affymetrix, Illumina [509981] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90080041 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.0: Atrioventricular block, first degree (Gene-based burden) 1,545 European ancestry cases, 386,385 European ancestry controls NA Illumina [185344] 0 First degree atrioventricular block http://purl.obolibrary.org/obo/HP_0011705 GCST90083987 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L30.9: Dermatitis, unspecified 1,998 European ancestry cases, 385,119 European ancestry controls NA Affymetrix, Illumina [509981] 0 dermatitis http://purl.obolibrary.org/obo/MONDO_0002406 GCST90080345 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.1: Atrioventricular block, second degree (Gene-based burden) 650 European ancestry cases, 387,280 European ancestry controls NA Illumina [185344] 0 Second degree atrioventricular block http://purl.obolibrary.org/obo/HP_0011706 GCST90083988 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R49.0: Dysphonia 1,188 European ancestry cases, 385,932 European ancestry controls NA Affymetrix, Illumina [509981] 0 voice disorders http://www.ebi.ac.uk/efo/EFO_0009692 GCST90080865 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.2: Atrioventricular block, complete (Gene-based burden) 841 European ancestry cases, 387,048 European ancestry controls NA Illumina [185344] 0 atrioventricular block http://purl.obolibrary.org/obo/MONDO_0000465 GCST90083989 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I35: Nonrheumatic aortic valve disorders 3,782 European ancestry cases, 383,293 European ancestry controls NA Affymetrix, Illumina [509980] 0 aortic valve disease http://www.ebi.ac.uk/efo/EFO_0009531 GCST90079996 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.7: Left bundle-branch block, unspecified (Gene-based burden) 2,509 European ancestry cases, 385,261 European ancestry controls NA Illumina [185343] 0 Left bundle branch block http://purl.obolibrary.org/obo/HP_0011713 GCST90083990 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.011.: Encounter for initial prescription of contraceptive pills 1,215 European ancestry cases, 385,879 European ancestry controls NA Affymetrix, Illumina [509979] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081230 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I45: Other conduction disorders (Gene-based burden) 3,184 European ancestry cases, 384,091 European ancestry controls NA Illumina [185332] 0 conduction system disorder http://www.ebi.ac.uk/efo/EFO_0005137 GCST90083993 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40: Epilepsy and recurrent seizures 4,885 European ancestry cases, 382,224 European ancestry controls NA Affymetrix, Illumina [509977] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90079825 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I45.1: Other and unspecified right bundle-branch block (Gene-based burden) 2,241 European ancestry cases, 385,689 European ancestry controls NA Illumina [185344] 0 Right bundle branch block http://purl.obolibrary.org/obo/HP_0011712 GCST90083992 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.60: Unspecified fracture of lower end of ulna 862 European ancestry cases, 386,222 European ancestry controls NA Affymetrix, Illumina [509974] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080989 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I46: Cardiac arrest (Gene-based burden) 1,488 European ancestry cases, 386,316 European ancestry controls NA Illumina [185342] 0 GCST90083996 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.1: Family history of malignant neoplasm of trachea, bronchus and lung 551 European ancestry cases, 386,553 European ancestry controls NA Affymetrix, Illumina [509972] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90081330 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I46.0: Cardiac arrest with successful resuscitation (Gene-based burden) 895 European ancestry cases, 387,035 European ancestry controls NA Illumina [81555] 0 GCST90083994 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20.0: Calculus of kidney 3,998 European ancestry cases, 383,150 European ancestry controls NA Affymetrix, Illumina [509968] 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90080586 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I46.9: Cardiac arrest, cause unspecified (Gene-based burden) 695 European ancestry cases, 387,131 European ancestry controls NA Illumina [185341] 0 GCST90083995 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20.0: Anesthesia of skin 887 European ancestry cases, 383,058 European ancestry controls NA Affymetrix, Illumina [507077] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080814 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.9: Arthritis, unspecified (Gene-based burden) 15,502 European ancestry cases, 372,428 European ancestry controls NA Illumina [185344] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90084390 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41: Other symptoms and signs involving cognitive functions and awareness 5,710 European ancestry cases, 378,069 European ancestry controls NA Affymetrix, Illumina [507058] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90080857 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.90: Arthritis, unspecified (Gene-based burden) 1,283 European ancestry cases, 386,647 European ancestry controls NA Illumina [185344] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90084385 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.8: Other specified hearing loss 1,017 European ancestry cases, 382,861 European ancestry controls NA Affymetrix, Illumina [507057] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90079948 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.94: Arthritis, unspecified (Gene-based burden) 1,004 European ancestry cases, 386,926 European ancestry controls NA Illumina [185344] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90084386 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.8X9.: Other specified hearing loss, unspecified ear 940 European ancestry cases, 382,934 European ancestry controls NA Affymetrix, Illumina [507053] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90079947 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.8: Other abnormalities of breathing (Gene-based burden) 2,031 European ancestry cases, 383,067 European ancestry controls NA Illumina [185282] 0 Abnormal pattern of respiration http://purl.obolibrary.org/obo/HP_0002793 GCST90084757 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91: Personal risk factors, not elsewhere classified 13,623 European ancestry cases, 349,764 European ancestry controls NA Affymetrix, Illumina [489134] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90081403 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.83: Snoring (Gene-based burden) 879 European ancestry cases, 384,413 European ancestry controls NA Illumina [185290] 0 Snoring http://purl.obolibrary.org/obo/HP_0025267 GCST90084756 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myocardial infarction 15,475 European ancestry cases, 348,048 European ancestry controls NA Affymetrix, Illumina [488933] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90081494 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07: Pain in throat and chest (Gene-based burden) 44,606 European ancestry cases, 321,826 European ancestry controls NA Illumina [185017] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90084765 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z23: Encounter for immunization 20,430 European ancestry cases, 341,925 European ancestry controls NA Affymetrix, Illumina [488176] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081223 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.2: Precordial pain (Gene-based burden) 4,782 European ancestry cases, 382,966 European ancestry controls NA Illumina [185343] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90084759 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J02: Acute pharyngitis 10,891 European ancestry cases, 351,064 European ancestry controls NA Affymetrix, Illumina [487454] 0 acute pharyngitis http://www.ebi.ac.uk/efo/EFO_0009657 GCST90080087 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.3: Other chest pain (Gene-based burden) 10,838 European ancestry cases, 377,092 European ancestry controls NA Illumina [185344] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90084760 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic kidney disease 7,613 European ancestry cases, 354,119 European ancestry controls NA Affymetrix, Illumina [487259] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90081467 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.4: Chest pain, unspecified (Gene-based burden) 26,118 European ancestry cases, 361,812 European ancestry controls NA Illumina [185344] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90084761 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87: Personal history of other diseases and conditions 81,773 European ancestry cases, 279,736 European ancestry controls NA Affymetrix, Illumina [487009] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081380 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.8: Other chest pain (Gene-based burden) 2,766 European ancestry cases, 372,667 European ancestry controls NA Illumina [185114] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90084763 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L98: Other disorders of skin and subcutaneous tissue, not elsewhere classified 18,698 European ancestry cases, 342,663 European ancestry controls NA Affymetrix, Illumina [486996] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080384 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.89: Other chest pain (Gene-based burden) 2,521 European ancestry cases, 374,512 European ancestry controls NA Illumina [185131] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90084762 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cerebrovascular disease - ischemic composite (no atrial fibrillation) 6,889 European ancestry cases, 353,545 European ancestry controls NA Affymetrix, Illumina [486033] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90081471 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.9: Chest pain, unspecified (Gene-based burden) 9,797 European ancestry cases, 359,753 European ancestry controls NA Illumina [185070] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90084764 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J22: Unspecified acute lower respiratory infection 31,920 European ancestry cases, 328,167 European ancestry controls NA Affymetrix, Illumina [485988] 0 lower respiratory tract disease http://www.ebi.ac.uk/efo/EFO_0009433 GCST90080101 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J39.2: Other diseases of pharynx 682 European ancestry cases, 386,581 European ancestry controls NA Affymetrix, Illumina [510127] 0 disorder of pharynx http://purl.obolibrary.org/obo/MONDO_0020592 GCST90080123 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20.0: Unstable angina (Gene-based burden) 6,110 European ancestry cases, 381,435 European ancestry controls NA Illumina [185340] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90083951 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K90: Intestinal malabsorption 2,759 European ancestry cases, 384,510 European ancestry controls 2,009 European ancestry cases, 111,270 European ancestry controls Affymetrix, Illumina [510114] 0 malabsorption syndrome http://www.ebi.ac.uk/efo/EFO_0009554 GCST90080315 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20.8: Other forms of angina pectoris (Gene-based burden) 1,225 European ancestry cases, 386,705 European ancestry controls NA Illumina [185344] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90083952 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L02.4: Cutaneous abscess, furuncle and carbuncle of limb 1,320 European ancestry cases, 385,927 European ancestry controls NA Affymetrix, Illumina [510106] 0 Cutaneous abscess http://purl.obolibrary.org/obo/HP_0031292 GCST90080325 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20.9: Angina pectoris, unspecified (Gene-based burden) 18,859 European ancestry cases, 369,024 European ancestry controls NA Illumina [185344] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90083953 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.4: Family history of malignant neoplasm of genital organs 1,416 European ancestry cases, 385,868 European ancestry controls 1,771 European ancestry cases, 33,532 European ancestry controls Affymetrix, Illumina [510103] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90081332 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21: Acute myocardial infarction (Gene-based burden) 10,907 European ancestry cases, 375,797 European ancestry controls NA Illumina [185321] 0 acute myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008583 GCST90083959 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.9: Spondylosis, unspecified 4,418 European ancestry cases, 382,756 European ancestry controls NA Affymetrix, Illumina [510096] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080485 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.0: ST elevation (STEMI) myocardial infarction of anterior wall (Gene-based burden) 1,954 European ancestry cases, 385,976 European ancestry controls NA Illumina [185344] 0 ST Elevation Myocardial Infarction http://www.ebi.ac.uk/efo/EFO_0008585 GCST90083955 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E83: Disorders of mineral metabolism 3,300 European ancestry cases, 383,907 European ancestry controls 7,215 European ancestry cases, 83,908 European ancestry controls Affymetrix, Illumina [510095] 0 mineral metabolism disease http://www.ebi.ac.uk/efo/EFO_0009556 GCST90079772 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.1: ST elevation (STEMI) myocardial infarction of inferior wall (Gene-based burden) 2,404 European ancestry cases, 385,526 European ancestry controls NA Illumina [185342] 0 ST Elevation Myocardial Infarction http://www.ebi.ac.uk/efo/EFO_0008585 GCST90083956 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D51: Vitamin B12 deficiency anemia 1,370 European ancestry cases, 385,838 European ancestry controls NA Affymetrix, Illumina [510083] 0 vitamin B12 deficiency http://www.ebi.ac.uk/efo/EFO_0000734 GCST90079706 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.4: Non-ST elevation (NSTEMI) myocardial infarction (Gene-based burden) 1,862 European ancestry cases, 386,068 European ancestry controls NA Illumina [185344] 0 Non-ST Elevation Myocardial Infarction http://www.ebi.ac.uk/efo/EFO_0008586 GCST90083957 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C80: Malignant neoplasm without specification of site 2,342 European ancestry cases, 384,910 European ancestry controls 556 European ancestry cases, 121,476 European ancestry controls Affymetrix, Illumina [510082] 0 GCST90079632 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.9: Acute myocardial infarction, unspecified (Gene-based burden) 5,398 European ancestry cases, 381,223 European ancestry controls NA Illumina [185314] 0 acute myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008583 GCST90083958 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.6: Stiffness of joint, not elsewhere classified 803 European ancestry cases, 386,439 European ancestry controls NA Affymetrix, Illumina [510082] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90080461 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I22: Subsequent ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction (Gene-based burden) 760 European ancestry cases, 387,165 European ancestry controls NA Illumina [185344] 0 Subsequent ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008584 GCST90083960 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.4: Fracture of shaft of fibula 524 European ancestry cases, 386,685 European ancestry controls NA Affymetrix, Illumina [510071] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081022 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I24: Other acute ischemic heart diseases (Gene-based burden) 2,133 European ancestry cases, 385,287 European ancestry controls NA Illumina [185339] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90083963 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L92: Granulomatous disorders of skin and subcutaneous tissue 825 European ancestry cases, 386,387 European ancestry controls NA Affymetrix, Illumina [510054] 0 granulomatous dermatitis http://www.ebi.ac.uk/efo/EFO_1000705 GCST90080380 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I24.8: Other forms of acute ischemic heart disease (Gene-based burden) 749 European ancestry cases, 387,181 European ancestry controls NA Illumina [185344] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90083961 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J47: Bronchiectasis 3,053 European ancestry cases, 384,169 European ancestry controls NA Affymetrix, Illumina [510052] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90080142 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I24.9: Acute ischemic heart disease, unspecified (Gene-based burden) 1,039 European ancestry cases, 386,891 European ancestry controls NA Illumina [185344] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90083962 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R54: Age-related physical debility 756 European ancestry cases, 386,430 European ancestry controls NA Affymetrix, Illumina [510050] 0 functional decline measurement http://www.ebi.ac.uk/efo/EFO_0007784 GCST90080879 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M05.9: Rheumatoid arthritis with rheumatoid factor, unspecified (Gene-based burden) 654 European ancestry cases, 387,206 European ancestry controls NA Illumina [185344] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90084372 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K20: Esophagitis 12,056 European ancestry cases, 371,916 European ancestry controls NA Affymetrix, Illumina [507190] 0 Esophagitis http://purl.obolibrary.org/obo/HP_0100633 GCST90080185 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06: Other rheumatoid arthritis (Gene-based burden) 6,100 European ancestry cases, 379,952 European ancestry controls NA Illumina [185312] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90084378 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.9: Unspecified fracture of lower leg 701 European ancestry cases, 383,185 European ancestry controls NA Affymetrix, Illumina [507186] 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90081028 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.0: Rheumatoid arthritis without rheumatoid factor (Gene-based burden) 706 European ancestry cases, 385,886 European ancestry controls NA Illumina [185327] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90084374 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B00: Herpesviral [herpes simplex] infections 1,285 European ancestry cases, 382,676 European ancestry controls NA Affymetrix, Illumina [507182] 0 Herpesviridae infectious disease http://www.ebi.ac.uk/efo/EFO_0007309 GCST90079548 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.9: Rheumatoid arthritis, unspecified (Gene-based burden) 5,220 European ancestry cases, 382,668 European ancestry controls NA Illumina [185344] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90084377 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.90: Unspecified fracture of unspecified lower leg 684 European ancestry cases, 383,198 European ancestry controls NA Affymetrix, Illumina [507181] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081027 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.90: Rheumatoid arthritis, unspecified (Gene-based burden) 1,306 European ancestry cases, 386,624 European ancestry controls NA Illumina [185344] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90084375 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45: Asthma 39,436 European ancestry cases, 344,538 European ancestry controls 19,108 European ancestry cases, 90,352 European ancestry controls Affymetrix, Illumina [507178] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90080141 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.99: Rheumatoid arthritis, unspecified (Gene-based burden) 2,622 European ancestry cases, 385,308 European ancestry controls NA Illumina [185344] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90084376 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B36: Other superficial mycoses 880 European ancestry cases, 383,055 European ancestry controls NA Affymetrix, Illumina [507170] 0 cutaneous mycosis http://purl.obolibrary.org/obo/MONDO_0000254 GCST90079554 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M07: Enteropathic arthropathies (Gene-based burden) 906 European ancestry cases, 387,013 European ancestry controls NA Illumina [19298] 0 Arthropathy http://purl.obolibrary.org/obo/HP_0003040 GCST90084379 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.89: Other long term (current) drug therapy 1,743 European ancestry cases, 382,184 European ancestry controls NA Affymetrix, Illumina [507154] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081326 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10: Gout (Gene-based burden) 7,961 European ancestry cases, 375,561 European ancestry controls NA Illumina [185277] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90084382 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S33.5: Sprain of ligaments of lumbar spine 701 European ancestry cases, 383,115 European ancestry controls NA Affymetrix, Illumina [507133] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080971 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10.9: Gout, unspecified (Gene-based burden) 4,531 European ancestry cases, 383,393 European ancestry controls NA Illumina [185344] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90084381 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K12: Stomatitis and related lesions 1,778 European ancestry cases, 382,114 European ancestry controls NA Affymetrix, Illumina [507123] 0 stomatitis http://www.ebi.ac.uk/efo/EFO_0009688 GCST90080179 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10.99: Gout, unspecified (Gene-based burden) 1,845 European ancestry cases, 386,085 European ancestry controls NA Illumina [185344] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90084380 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51: Encounter for other aftercare and medical care 34,913 European ancestry cases, 348,833 European ancestry controls 29,153 European ancestry cases, 79,352 European ancestry controls Affymetrix, Illumina [507098] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081286 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M11: Other crystal arthropathies (Gene-based burden) 581 European ancestry cases, 387,116 European ancestry controls NA Illumina [185344] 0 crystal arthropathy http://purl.obolibrary.org/obo/MONDO_0022208 GCST90084383 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.1: Patient's noncompliance with medical treatment and regimen 1,566 European ancestry cases, 382,234 European ancestry controls NA Affymetrix, Illumina [507094] 0 medication adherence behavior http://www.ebi.ac.uk/efo/EFO_0006344 GCST90081398 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13: Other arthritis (Gene-based burden) 17,422 European ancestry cases, 365,539 European ancestry controls NA Illumina [185294] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90084391 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z02: Encounter for administrative examination 5,475 European ancestry cases, 378,305 European ancestry controls NA Affymetrix, Illumina [507090] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081187 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.0: Polyarthritis, unspecified (Gene-based burden) 784 European ancestry cases, 386,900 European ancestry controls NA Illumina [185342] 0 polyarticular arthritis http://purl.obolibrary.org/obo/MONDO_0024280 GCST90084384 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.998.: Other and unspecified abnormal findings in urine (Gene-based burden) 5,824 European ancestry cases, 371,752 European ancestry controls NA Illumina [185156] 0 Abnormality of urine homeostasis http://purl.obolibrary.org/obo/HP_0003110 GCST90084901 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nasal sinus disorder 1,740 European ancestry cases, 330,014 European ancestry controls NA Affymetrix, Illumina [458873] 0 paranasal sinus disease http://www.ebi.ac.uk/efo/EFO_0009481 GCST90077832 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87: Abnormal findings in specimens from female genital organs (Gene-based burden) 13,074 European ancestry cases, 176,246 European ancestry controls NA Illumina [178367] 0 Abnormal morphology of female internal genitalia http://purl.obolibrary.org/obo/HP_0000008 GCST90084909 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nervous breakdown 669 European ancestry cases, 331,085 European ancestry controls NA Affymetrix, Illumina [458873] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90077765 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.6: Abnormal cytological findings in specimens from female genital organs (Gene-based burden) 12,550 European ancestry cases, 177,618 European ancestry controls NA Illumina [178451] 0 Abnormal morphology of female internal genitalia http://purl.obolibrary.org/obo/HP_0000008 GCST90084908 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oesophagitis barretts oesophagus 1,490 European ancestry cases, 330,264 European ancestry controls NA Affymetrix, Illumina [458873] 0 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90077694 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.61: Abnormal cytological findings in specimens from cervix uteri (Gene-based burden) 11,386 European ancestry cases, 354,659 European ancestry controls NA Illumina [184963] 0 Abnormal morphology of female internal genitalia http://purl.obolibrary.org/obo/HP_0000008 GCST90084907 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteoarthritis 39,005 European ancestry cases, 292,749 European ancestry controls NA Affymetrix, Illumina [458873] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90077875 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.615.: Unsatisfactory cytologic smear of cervix (Gene-based burden) 5,620 European ancestry cases, 368,302 European ancestry controls NA Illumina [185143] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084905 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteomyelitis 688 European ancestry cases, 331,066 European ancestry controls NA Affymetrix, Illumina [458873] 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90077777 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.618.: Other abnormal cytological findings on specimens from cervix uteri (Gene-based burden) 6,536 European ancestry cases, 369,132 European ancestry controls NA Illumina [185108] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084906 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteopenia 1,605 European ancestry cases, 330,149 European ancestry controls NA Affymetrix, Illumina [458873] 0 Osteopenia http://purl.obolibrary.org/obo/HP_0000938 GCST90077961 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R89: Abnormal findings in specimens from other organs, systems and tissues (Gene-based burden) 3,179 European ancestry cases, 376,895 European ancestry controls NA Illumina [185261] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084912 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Osteoporosis 7,730 European ancestry cases, 324,024 European ancestry controls NA Affymetrix, Illumina [458873] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90077779 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R89.5: Abnormal microbiological findings in specimens from other organs, systems and tissues (Gene-based burden) 831 European ancestry cases, 383,408 European ancestry controls NA Illumina [185303] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084910 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other joint disorder 2,706 European ancestry cases, 329,048 European ancestry controls NA Affymetrix, Illumina [458873] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90077879 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R89.9: Unspecified abnormal finding in specimens from other organs, systems and tissues (Gene-based burden) 2,049 European ancestry cases, 382,289 European ancestry controls NA Illumina [185307] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084911 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other neurological problem 1,794 European ancestry cases, 329,960 European ancestry controls NA Affymetrix, Illumina [458873] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90077842 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R91: Abnormal findings on diagnostic imaging of lung (Gene-based burden) 3,443 European ancestry cases, 384,244 European ancestry controls NA Illumina [185343] 0 Abnormal lung morphology http://purl.obolibrary.org/obo/HP_0002088 GCST90084913 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other renal or kidney problem 1,957 European ancestry cases, 329,797 European ancestry controls NA Affymetrix, Illumina [458873] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90077824 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R92: Abnormal and inconclusive findings on diagnostic imaging of breast (Gene-based burden) 927 European ancestry cases, 207,749 European ancestry controls NA Illumina [179712] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084915 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ovarian cyst or cysts 3,831 European ancestry cases, 327,923 European ancestry controls NA Affymetrix, Illumina [458873] 0 Ovarian cyst http://purl.obolibrary.org/obo/HP_0000138 GCST90077793 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R92.8: Other abnormal and inconclusive findings on diagnostic imaging of breast (Gene-based burden) 870 European ancestry cases, 383,723 European ancestry controls NA Illumina [185261] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084914 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pancreatitis 980 European ancestry cases, 330,774 European ancestry controls NA Affymetrix, Illumina [458873] 0 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90077706 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93: Abnormal findings on diagnostic imaging of other body structures (Gene-based burden) 5,929 European ancestry cases, 373,345 European ancestry controls NA Illumina [185248] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90084919 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.9: Hyperglycemia, unspecified (Gene-based burden) 899 European ancestry cases, 385,804 European ancestry controls NA Illumina [185319] 0 Hyperglycemia http://purl.obolibrary.org/obo/HP_0003074 GCST90084891 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Liver, biliary or pancreas problem 796 European ancestry cases, 330,958 European ancestry controls NA Affymetrix, Illumina [458873] 0 biliary tract disease, pancreas disease, liver disease http://www.ebi.ac.uk/efo/EFO_0009534, http://www.ebi.ac.uk/efo/EFO_0009605, http://www.ebi.ac.uk/efo/EFO_0001421 GCST90077689 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R74: Abnormal serum enzyme levels (Gene-based burden) 652 European ancestry cases, 386,128 European ancestry controls NA Illumina [185312] 0 abnormality of serum enzyme levels http://www.ebi.ac.uk/efo/EFO_0009826 GCST90084894 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malabsorption coeliac disease 1,968 European ancestry cases, 329,786 European ancestry controls NA Affymetrix, Illumina [458873] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90077859 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R74.8: Abnormal levels of other serum enzymes (Gene-based burden) 527 European ancestry cases, 386,424 European ancestry controls NA Illumina [185316] 0 abnormality of serum enzyme levels http://www.ebi.ac.uk/efo/EFO_0009826 GCST90084893 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mania bipolar disorder manic depression 1,240 European ancestry cases, 330,514 European ancestry controls NA Affymetrix, Illumina [458873] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90077767 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R79: Other abnormal findings of blood chemistry (Gene-based burden) 11,799 European ancestry cases, 370,234 European ancestry controls NA Illumina [185261] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084897 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Measles morbillivirus 6,073 European ancestry cases, 325,681 European ancestry controls NA Affymetrix, Illumina [458873] 0 measles http://www.ebi.ac.uk/efo/EFO_1002025 GCST90077941 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R79.8: Other specified abnormal findings of blood chemistry (Gene-based burden) 11,085 European ancestry cases, 371,365 European ancestry controls NA Illumina [185271] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084896 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Menieres disease 1,297 European ancestry cases, 330,457 European ancestry controls NA Affymetrix, Illumina [458873] 0 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90077840 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R79.89: Other specified abnormal findings of blood chemistry (Gene-based burden) 3,082 European ancestry cases, 379,295 European ancestry controls NA Illumina [185268] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084895 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Meningitis 1,865 European ancestry cases, 329,889 European ancestry controls NA Affymetrix, Illumina [458873] 0 infectious meningitis http://www.ebi.ac.uk/efo/EFO_0000584 GCST90077734 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R80: Proteinuria (Gene-based burden) 1,218 European ancestry cases, 384,665 European ancestry controls NA Illumina [185313] 0 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90084899 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Migraine 14,131 European ancestry cases, 317,623 European ancestry controls NA Affymetrix, Illumina [458873] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90077745 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R80.9: Proteinuria, unspecified (Gene-based burden) 847 European ancestry cases, 385,062 European ancestry controls NA Illumina [185313] 0 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90084898 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple sclerosis 1,596 European ancestry cases, 330,158 European ancestry controls NA Affymetrix, Illumina [458873] 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90077739 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82: Other and unspecified abnormal findings in urine (Gene-based burden) 9,916 European ancestry cases, 361,639 European ancestry controls NA Illumina [185093] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084904 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mumps epidemic parotitis 3,743 European ancestry cases, 328,011 European ancestry controls NA Affymetrix, Illumina [458873] 0 Mumps virus infectious disease http://www.ebi.ac.uk/efo/EFO_0007383 GCST90077943 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.8: Abnormal findings on cytological and histological examination of urine (Gene-based burden) 2,479 European ancestry cases, 382,756 European ancestry controls NA Illumina [185316] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084900 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Muscle or soft tissue injuries 3,750 European ancestry cases, 328,004 European ancestry controls NA Affymetrix, Illumina [458873] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90077826 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.9: Other and unspecified abnormal findings in urine (Gene-based burden) 7,472 European ancestry cases, 366,444 European ancestry controls NA Illumina [185117] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90084903 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Muscle or soft tissue problem 3,644 European ancestry cases, 328,110 European ancestry controls NA Affymetrix, Illumina [458873] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90077775 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.99: Other abnormal findings in urine (Gene-based burden) 7,200 European ancestry cases, 366,949 European ancestry controls NA Illumina [185118] 0 Abnormality of urine homeostasis http://purl.obolibrary.org/obo/HP_0003110 GCST90084902 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nasal polyps 2,016 European ancestry cases, 329,738 European ancestry controls NA Affymetrix, Illumina [458873] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90077838 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63: Symptoms and signs concerning food and fluid intake (Gene-based burden) 9,824 European ancestry cases, 372,091 European ancestry controls NA Illumina [185212] 0 sign or symptom concerning food and fluid intake http://www.ebi.ac.uk/efo/EFO_0009825 GCST90084882 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63.0: Anorexia (Gene-based burden) 1,199 European ancestry cases, 385,979 European ancestry controls NA Illumina [185330] 0 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST90084879 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63.4: Abnormal weight loss (Gene-based burden) 7,833 European ancestry cases, 378,297 European ancestry controls NA Illumina [185310] 0 body weight loss http://www.ebi.ac.uk/efo/EFO_0005245 GCST90084880 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63.8: Other symptoms and signs concerning food and fluid intake (Gene-based burden) 896 European ancestry cases, 385,040 European ancestry controls NA Illumina [185294] 0 sign or symptom concerning food and fluid intake http://www.ebi.ac.uk/efo/EFO_0009825 GCST90084881 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hypothyroidism or myxoedema 22,064 European ancestry cases, 309,690 European ancestry controls 25,043 European ancestry cases, 90,108 European ancestry controls Affymetrix, Illumina [458873] 1 myxedema, hypothyroidism http://www.ebi.ac.uk/efo/EFO_1001055, http://www.ebi.ac.uk/efo/EFO_0004705 GCST90077730 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R68: Other general symptoms and signs (Gene-based burden) 5,024 European ancestry cases, 370,295 European ancestry controls NA Illumina [185131] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90084885 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Infectious mononucleosis glandular fever epstein barr virus ebv 1,070 European ancestry cases, 330,684 European ancestry controls NA Affymetrix, Illumina [458873] 0 infectious mononucleosis http://www.ebi.ac.uk/efo/EFO_0007326 GCST90077939 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R68.8: Other general symptoms and signs (Gene-based burden) 4,834 European ancestry cases, 370,577 European ancestry controls NA Illumina [185132] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90084884 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Infective viral hepatitis 979 European ancestry cases, 330,775 European ancestry controls NA Affymetrix, Illumina [458873] 0 viral human hepatitis infection http://www.ebi.ac.uk/efo/EFO_0004196 GCST90077702 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R68.89: Other general symptoms and signs (Gene-based burden) 4,075 European ancestry cases, 371,328 European ancestry controls NA Illumina [185135] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90084883 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Iron deficiency anaemia 2,724 European ancestry cases, 329,030 European ancestry controls NA Affymetrix, Illumina [458873] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90077787 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R69: Illness, unspecified (Gene-based burden) 17,480 European ancestry cases, 369,056 European ancestry controls NA Illumina [185329] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90084886 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Irregular heart beat 1,046 European ancestry cases, 330,708 European ancestry controls NA Affymetrix, Illumina [458873] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90077897 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73: Elevated blood glucose level (Gene-based burden) 4,283 European ancestry cases, 374,702 European ancestry controls NA Illumina [185167] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90084892 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Irritable bowel syndrome 11,343 European ancestry cases, 320,411 European ancestry controls NA Affymetrix, Illumina [458873] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90077699 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.0: Abnormal glucose (Gene-based burden) 3,431 European ancestry cases, 376,474 European ancestry controls NA Illumina [185189] 0 Abnormal glucose homeostasis http://purl.obolibrary.org/obo/HP_0011014 GCST90084890 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Jaundice unknown cause 630 European ancestry cases, 331,124 European ancestry controls NA Affymetrix, Illumina [458873] 0 Jaundice http://purl.obolibrary.org/obo/HP_0000952 GCST90077907 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.01: Impaired fasting glucose (Gene-based burden) 587 European ancestry cases, 385,372 European ancestry controls NA Illumina [185311] 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90084887 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Joint disorder 2,082 European ancestry cases, 329,672 European ancestry controls NA Affymetrix, Illumina [458873] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90077773 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.02: Impaired glucose tolerance (oral) (Gene-based burden) 712 European ancestry cases, 384,821 European ancestry controls NA Illumina [185299] 0 abnormal glucose tolerance http://www.ebi.ac.uk/efo/EFO_0002546 GCST90084888 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Joint pain 2,226 European ancestry cases, 329,528 European ancestry controls NA Affymetrix, Illumina [458873] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90077925 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.09: Other abnormal glucose (Gene-based burden) 1,839 European ancestry cases, 381,747 European ancestry controls NA Illumina [185265] 0 Abnormal blood glucose concentration http://purl.obolibrary.org/obo/HP_0011015 GCST90084889 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Parkinsons disease 828 European ancestry cases, 330,926 European ancestry controls NA Affymetrix, Illumina [458873] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90077741 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93.1: Abnormal findings on diagnostic imaging of heart and coronary circulation (Gene-based burden) 917 European ancestry cases, 385,023 European ancestry controls NA Illumina [185323] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90084916 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peripheral neuropathy 691 European ancestry cases, 331,063 European ancestry controls NA Affymetrix, Illumina [458873] 0 peripheral neuropathy http://www.ebi.ac.uk/efo/EFO_0003100 GCST90077736 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93.3: Abnormal findings on diagnostic imaging of other parts of digestive tract (Gene-based burden) 2,213 European ancestry cases, 383,145 European ancestry controls NA Illumina [185326] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90084917 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peripheral vascular disease 813 European ancestry cases, 330,941 European ancestry controls NA Affymetrix, Illumina [458873] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90077649 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93.8: Abnormal findings on diagnostic imaging of other specified body structures (Gene-based burden) 687 European ancestry cases, 386,003 European ancestry controls NA Illumina [185331] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90084918 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peritonitis 1,501 European ancestry cases, 330,253 European ancestry controls NA Affymetrix, Illumina [458873] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90077708 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94: Abnormal results of function studies (Gene-based burden) 8,623 European ancestry cases, 367,496 European ancestry controls NA Illumina [185174] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90084923 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pernicious anaemia 1,382 European ancestry cases, 330,372 European ancestry controls NA Affymetrix, Illumina [458873] 0 pernicious anemia http://www.ebi.ac.uk/efo/EFO_0005576 GCST90077789 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94.2: Abnormal results of pulmonary function studies (Gene-based burden) 938 European ancestry cases, 384,331 European ancestry controls NA Illumina [185302] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90084920 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pleurisy 1,711 European ancestry cases, 330,043 European ancestry controls NA Affymetrix, Illumina [458873] 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90077683 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94.3: Abnormal results of cardiovascular function studies (Gene-based burden) 1,315 European ancestry cases, 381,670 European ancestry controls NA Illumina [185271] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90084921 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pneumonia 6,965 European ancestry cases, 324,789 European ancestry controls NA Affymetrix, Illumina [458873] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90077819 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94.5: Abnormal results of liver function studies (Gene-based burden) 5,893 European ancestry cases, 378,855 European ancestry controls NA Illumina [185302] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90084922 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Polymyalgia rheumatica 1,059 European ancestry cases, 330,695 European ancestry controls NA Affymetrix, Illumina [458873] 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90077808 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00: Superficial injury of head (Gene-based burden) 3,216 European ancestry cases, 383,001 European ancestry controls NA Illumina [185308] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90084927 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Post natal depression 547 European ancestry cases, 331,207 European ancestry controls NA Affymetrix, Illumina [458873] 0 postpartum depression http://www.ebi.ac.uk/efo/EFO_0007453 GCST90077920 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00.0: Superficial injury of scalp (Gene-based burden) 537 European ancestry cases, 386,906 European ancestry controls NA Illumina [185339] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084924 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prolapsed disc or slipped disc 7,846 European ancestry cases, 323,908 European ancestry controls NA Affymetrix, Illumina [458873] 0 vertebral joint disease http://www.ebi.ac.uk/efo/EFO_0009477 GCST90077783 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00.8: Superficial injury of other parts of head (Gene-based burden) 1,368 European ancestry cases, 386,390 European ancestry controls NA Illumina [185339] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084925 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Psoriasis 5,389 European ancestry cases, 326,365 European ancestry controls 4,001 European ancestry cases, 118,929 European ancestry controls Affymetrix, Illumina [458873] 1 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90077855 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00.9: Superficial injury of unspecified part of head (Gene-based burden) 714 European ancestry cases, 386,310 European ancestry controls NA Illumina [185321] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084926 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Psoriatic arthropathy 870 European ancestry cases, 330,884 European ancestry controls NA Affymetrix, Illumina [458873] 0 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90077889 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S01: Open wound of head (Gene-based burden) 4,083 European ancestry cases, 382,522 European ancestry controls NA Illumina [185335] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90084930 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulmonary embolism 3,685 European ancestry cases, 328,069 European ancestry controls NA Affymetrix, Illumina [458873] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90077667 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High cholesterol 57,365 European ancestry cases, 274,389 European ancestry controls NA Affymetrix, Illumina [458873] 2 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90077883 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hypertension 115,454 European ancestry cases, 216,300 European ancestry controls 65,295 European ancestry cases, 53,444 European ancestry controls Affymetrix, Illumina [458873] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90077645 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hyperthyroidism or thyrotoxicosis 3,510 European ancestry cases, 328,244 European ancestry controls NA Affymetrix, Illumina [458873] 0 hyperthyroidism, Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009189, http://www.ebi.ac.uk/efo/EFO_0009190 GCST90077728 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Kidney stone ureter stone bladder stone 3,697 European ancestry cases, 328,057 European ancestry controls NA Affymetrix, Illumina [458873] 0 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90077712 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2020-12-08 32915782 Spracklen CN 2020-09-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32915782 Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences. Adiponectin levels (BMI-adjusted) 9,262 European ancestry individuals NA Illumina [16607452] (imputed) 12 BMI-adjusted adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0007737 GCST90011881 Genome-wide genotyping array 2020-12-08 32915782 Spracklen CN 2020-09-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32915782 Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences. Adiponectin levels (fat percentage adjusted) 9,262 European ancestry individuals NA Illumina [16607452] (imputed) 0 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90011882 Genome-wide genotyping array 2020-12-08 32915782 Spracklen CN 2020-09-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32915782 Adiponectin GWAS loci harboring extensive allelic heterogeneity exhibit distinct molecular consequences. Adiponectin levels (BMI-adjusted) 9,262 European ancestry individuals NA Illumina [39120605] (imputed) 0 BMI-adjusted adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0007737 GCST90011883 Genome-wide genotyping array 2022-01-31 33910371 Stanislawski MA 2021-04-29 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/33910371 Soluble CD14 Levels in the Jackson Heart Study: Associations With Cardiovascular Disease Risk and Genetic Variants. Soluble CD14 levels 3,349 Black individuals NA NR [31143179] 3 soluble CD14 measurement http://www.ebi.ac.uk/efo/EFO_0020860 GCST90093300 Genome-wide sequencing 2021-12-13 34608871 Chakraborty S 2021-01-01 J Genet www.ncbi.nlm.nih.gov/pubmed/34608871 A genomewide association study on individuals with occludable angles identifies potential risk loci for intraocular pressure. Intraocular pressure in individuals with narrow occludable anterior chamber angle 240 Indian ancestry individuals 89 Indian ancestry individuals Illumina [NR] 1 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90052901 Genome-wide genotyping array 2021-11-15 30659681 Lindstrom S 2019-01-19 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30659681 A large-scale exome array analysis of venous thromboembolism. Venous thromboembolism 8,332 European ancestry cases, 16,087 European ancestry controls, 382 African-American cases, 1,476 African-American controls NA Illumina [64794] 4 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST012523 Exome genotyping array [Exome array] 2021-12-15 34560273 Shadrin AA 2021-09-21 Neuroimage www.ncbi.nlm.nih.gov/pubmed/34560273 Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology. Cortical surface area 35,657 White British ancestry individuals NA NR [9056863] (imputed) 695 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90091060 Genome-wide genotyping array 2021-12-15 34560273 Shadrin AA 2021-09-21 Neuroimage www.ncbi.nlm.nih.gov/pubmed/34560273 Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology. Cortical thickness 35,657 White British ancestry individuals NA NR [9056863] (imputed) 539 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90091061 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(34:2)_[M+H]1+/Phosphatidylethanolamine-O(37:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060698 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(34:3)_[M+H]1+/Phosphatidylethanolamine-P(37:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060694 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(35:1)_[M+H]1+/Phosphatidylethanolamine-O(38:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060725 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(36:1)_[M+H]1+/Phosphatidylethanolamine-O(39:1)_[M+H]1+/Phosphatidylcholine-P(36:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 59 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060756 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(36:2)_[M+H]1+/Phosphatidylethanolamine-P(39:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060749 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(36:3)_M+H]1+/Phosphatidylcholine-P(36:2)_M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 69 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060744 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(36:4)_[M+H]1+/Phosphatidylcholine-P(36:3)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 9 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060740 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(36:5)_[M+H]1+/Phosphatidylcholine-P(36:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 165 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060735 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(37:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060787 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(37:1)_[M+H]1+/Phosphatidylethanolamine-O(40:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060780 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(37:2)_[M+H]1+/Phosphatidylethanolamine-O(40:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060773 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(38:1)_[M+H]1+/Phosphatidylethanolamine-P(41:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060816 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(38:2)_[M+H]1+/Phosphatidylcholine-P(38:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060811 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(38:4)_[M+H]1+/Phosphatidylcholine-P(38:3)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 24 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060801 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(38:5)_[M+H]1+/Phosphatidylcholine-P(38:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 77 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060796 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(39:1)_[M+H]1+/Phosphatidylethanolamine-P(39:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 25 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060842 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(39:2)_[M+H]1+/Phosphatidylethanolamine-P(39:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060839 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(39:3)_[M+H]1+/Phosphatidylethanolamine-P(39:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060834 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(40:5)_[M+H]1+/Phosphatidylcholine-P(40:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 68 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060855 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(40:6)_[M+H]1+/Phosphatidylcholine-P(40:5)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 51 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060851 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(40:7)_[M+H]1+/Phosphatidylcholine-P(40:6)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060846 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(40:9)_[M+H]1+/Phosphatidylethanolamine-P(40:8)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060837 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(42:11)_[M+H]1+/Phosphatidylcholine-P(42:10)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060879 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(46:1)_[M+H]1+/Phosphatidylcholine-P(46:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060983 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine-O(46:2)_[M+H]1+/Phosphatidylcholine-P(46:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060981 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:1)_[M+OAc]1-/Phosphatidylserine(38:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060845 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:2)_[M+H]1+/Phosphatidylethanolamine(37:2)_[M+H]1+/Phosphatidate(39:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 59 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060718 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:2)_[M+OAc]1-/Phosphatidylserine(38:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060841 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:3)_[M+H]1+/Phosphatidylethanolamine(37:3)_[M+H]1+/Phosphatidate(39:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060713 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:3)_[M+OAc]1-/Phosphatidylserine(38:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060836 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:4)_[M+H]1+/Phosphatidylethanolamine(37:4)_[M+H]1+/Phosphatidate(39:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060712 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:4)_[M+OAc]1-/Phosphatidylethanolamine(37:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060832 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(34:5)_[M+OAc]1-/Phosphatidylethanolamine(37:5)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060828 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(35:1)_[M+H]1+/Phosphatidylethanolamine(38:1)_[M+H]1+/Phosphatidate(40:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060755 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(35:2)_[M+H]1+/Phosphatidylethanolamine(38:2)_[M+H]1+/Phosphatidate(40:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060747 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(35:2)_[M+OAc]1-/Phosphatidylserine(39:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060862 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(35:3)_[M+H]1+/Phosphatidylethanolamine(38:3)_[M+H]1+/Phosphatidate(40:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 37 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060743 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(35:4)_[M+H]1+/Phosphatidylethanolamine(38:4)_[M+H]1+/Phosphatidate(40:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 124 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060738 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(35:6)_[M+OAc]1-/Phosphatidylserine(39:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060854 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:0)_[M+H]1+/Phosphatidylethanolamine(39:0)_[M+H]1+/Phosphatidate(41:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060786 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060893 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:1)_[M+H]1+/Phosphatidylethanolamine(39:1)_[M+H]1+/Phosphatidate(41:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060779 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:1)_[M+OAc]1-/Phosphatidylethanolamine(39:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060888 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:2)_[M+H]1+/Phosphatidylethanolamine(39:2)_[M+H]1+/Phosphatidate(41:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 43 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060772 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:2)_[M+OAc]1-/Phosphatidylserine(40:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060885 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:3)_[M+H]1+/Phosphatidylethanolamine(39:3)_[M+H]1+/Phosphatidate(41:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 111 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060766 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:3)_[M+OAc]1-/Phosphatidylserine(40:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 66 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060882 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:4)_[M+H]1+/Phosphatidylethanolamine(39:4)_[M+H]1+/Phosphatidate(41:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 13 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060762 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:4)_[M+OAc]1-/Phosphatidylserine(40:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060880 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:5)_[M+OAc]1-/Phosphatidylserine(40:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 68 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060878 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(18:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 81 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90060634 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(20:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 64 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90060650 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(20:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 129 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90060649 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl ester(20:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 75 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90060646 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Cholesteryl esteroxid(20:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90060658 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:8)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 9 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060861 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:8)_[M+OAc]1-/Phosphatidylserine(44:7)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060950 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:9)_[M+OAc]1-/Phosphatidylserine(44:8)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060947 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(42:11)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060977 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(42:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 60 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060990 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(42:5)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060986 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(43:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060951 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(43:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90061005 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(43:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90061004 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(45:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 17 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060982 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_25:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060186 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_34:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 13 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060253 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_34:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 10 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060250 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_34:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 49 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060247 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_35:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060260 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_36:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060279 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_36:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 30 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060276 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_36:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 42 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060274 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_36:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 27 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060272 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_37:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060304 Genome-wide genotyping array 2022-01-05 34524976 Nolan J 2021-09-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/34524976 Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3. Free thyroxine concentration 2,832 European ancestry individuals 1,104 European ancestry individuals Illumina [7522526] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90061527 Genome-wide genotyping array 2022-01-05 34524976 Nolan J 2021-09-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/34524976 Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3. Thyroid stimulating hormone levels 2,832 European ancestry individuals 1,104 European ancestry individuals Illumina [7522526] (imputed) 2 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST90061528 Genome-wide genotyping array 2022-01-05 34524976 Nolan J 2021-09-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/34524976 Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3. Thyroid peroxidase antibody levels 2,832 European ancestry individuals 1,104 European ancestry individuals Illumina [7522526] (imputed) 1 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST90061529 Genome-wide genotyping array 2022-01-05 34524976 Nolan J 2021-09-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/34524976 Genome-wide analysis of thyroid function in Australian adolescents highlights SERPINA7 and NCOA3. Free triiodothyronine (T3) levels 2,832 European ancestry individuals 1,104 European ancestry individuals Illumina [7522526] (imputed) 1 triiodothyronine measurement http://www.ebi.ac.uk/efo/EFO_0008392 GCST90061526 Genome-wide genotyping array 2021-10-20 34380480 Liu J 2021-08-12 BMC Med www.ncbi.nlm.nih.gov/pubmed/34380480 Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia. Schizophrenia 3,493 Han Chinese ancestry cases, 4,709 Han Chinese ancestry controls NA Illumina [3937527] (imputed) 3 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90053834 Genome-wide genotyping array 2021-10-20 34380480 Liu J 2021-08-12 BMC Med www.ncbi.nlm.nih.gov/pubmed/34380480 Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia. Schizophrenia 26,271 East Asian ancestry cases, 40,071 East Asian ancestry controls NA Illumina [NR] (imputed) 5 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90053835 Genome-wide genotyping array 2021-10-20 34380480 Liu J 2021-08-12 BMC Med www.ncbi.nlm.nih.gov/pubmed/34380480 Genome-wide association study followed by trans-ancestry meta-analysis identify 17 new risk loci for schizophrenia. Schizophrenia 26,271 East Asian ancestry cases, 40,071 East Asian ancestry controls, 33,640 European ancestry cases, 43,456 European ancestry controls NA Illumina [NR] (imputed) 16 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90053836 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 3 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061408 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 12am-2am) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061409 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 2am-4am) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 3 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061410 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 4am-6am) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061411 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 6am-8am) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061412 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 8am-10am) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061413 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 10am-12pm) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061414 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 12pm-2pm) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061415 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 2pm-4pm) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061416 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 4pm-6pm) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061417 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 6pm-8pm) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061418 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 8pm-10pm) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061419 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Total log acceleration 10pm-12am) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061420 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Light-intensity physical activity duration 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 3 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061421 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Moderate to vigorous physical activity duration 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061422 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Principal component 2) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061423 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Principal component 3) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061424 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Principal component 4) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061425 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Principal component 5) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061426 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Principal component 6) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061427 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Sedentary to active transition probability 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061428 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Active to sedentary transition probability 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061429 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Dynamic activity ratio estimate 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061430 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Average log acceleration during the five least active hours of the day 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061431 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Physical activity (Relative amplitude) 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061432 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Mid-point of the ten most active hours of the day 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061433 Genome-wide genotyping array 2022-02-03 35043453 Qi G 2022-01-18 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35043453 Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Mid-point of the five least active hours of the day 88,411 European ancestry individuals NA Affymetrix [8951705] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90061434 Genome-wide genotyping array 2021-12-07 34607834 Dawed AY 2021-10-04 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/34607834 Genome-Wide Meta-analysis Identifies Genetic Variants Associated With Glycemic Response to Sulfonylureas. Reduction in HbA1c levels in response to sulfonylureas treatment in type 2 diabetes 5,485 European ancestry individuals NA Affymetrix, Illumina [538635] (imputed) 15 HbA1c measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0004541, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90061380 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(34:0)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 17 diacylglycerol 34:0 measurement http://www.ebi.ac.uk/efo/EFO_0020058 GCST90060608 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(34:1)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 60 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90060607 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(34:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90060615 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(34:2)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 66 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90060606 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(34:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 2 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90060614 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(34:3)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 25 diacylglycerol 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0020059 GCST90060605 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:1)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 19 diacylglycerol 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010354 GCST90060613 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:2)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 56 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90060612 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 26 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90060625 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:3)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 59 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90060611 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 22 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90060623 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:4)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 18 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90060610 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90060621 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(36:5)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 diacylglycerol 36:5 measurement http://www.ebi.ac.uk/efo/EFO_0020064 GCST90060609 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(34:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060669 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(34:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060670 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(34:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060666 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(34:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060663 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(34:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 124 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060665 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(35:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060676 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060702 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060697 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060693 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060691 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 87 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060689 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 75 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060690 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060688 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(36:5)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060798 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(37:0)_[M+OAc]1-/Phosphatidylcholine(34:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060850 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(37:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060719 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(37:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060714 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(37:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060710 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(38:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060748 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(38:1)_[M+OAc]1-/Phosphatidylcholine(35:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060865 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(38:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060739 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(38:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060734 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(38:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 79 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060733 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(38:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060729 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(39:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060761 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(40:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 26 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060806 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(40:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060800 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(40:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060795 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(40:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060784 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(40:7)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 13 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060777 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_34:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060290 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_34:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060285 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_34:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060289 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_35:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060301 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_36:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060340 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_36:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060334 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pulmonary fibrosis 126 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Illumina [13429783] (imputed) 1 pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0009448 GCST90018688 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pyelonephritis 1,811 East Asian ancestry cases, 175,288 East Asian ancestry controls NA Illumina [13429797] (imputed) 1 pyelonephritis http://www.ebi.ac.uk/efo/EFO_1001141 GCST90018689 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Rheumatoid arthritis 5,348 East Asian ancestry cases, 173,268 East Asian ancestry controls NA Illumina [13429970] (imputed) 8 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90018690 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Retinal detachment 1,389 East Asian ancestry cases, 168,903 East Asian ancestry controls NA Illumina [13428804] (imputed) 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90018691 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Retinitis pigmentosa 155 East Asian ancestry cases, 168,903 East Asian ancestry controls NA Illumina [13428559] (imputed) 3 retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0019200 GCST90018692 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Rheumatic fever 152 East Asian ancestry cases, 170,247 East Asian ancestry controls NA Illumina [13428587] (imputed) 0 susceptibility to rheumatic fever measurement http://www.ebi.ac.uk/efo/EFO_0008416 GCST90018693 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ringworm 692 East Asian ancestry cases, 178,034 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 tinea http://www.ebi.ac.uk/efo/EFO_0007510 GCST90018694 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Stable angina pectoris 18,833 East Asian ancestry cases, 146,214 East Asian ancestry controls NA Illumina [13427711] (imputed) 28 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90018695 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Sleep apnea syndrome 473 East Asian ancestry cases, 177,864 East Asian ancestry controls NA Illumina [13429911] (imputed) 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90018696 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Systemic lupus erythematosus 317 East Asian ancestry cases, 175,937 East Asian ancestry controls NA Illumina [13429699] (imputed) 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90018697 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Sarcoidosis 220 East Asian ancestry cases, 177,667 East Asian ancestry controls NA Illumina [13429855] (imputed) 1 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90018698 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Schizophrenia 99 East Asian ancestry cases, 177,794 East Asian ancestry controls NA Illumina [13429798] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90018699 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Sjögren's syndrome 303 East Asian ancestry cases, 175,599 East Asian ancestry controls NA Illumina [13429612] (imputed) 1 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90018700 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Skin cancer 154 East Asian ancestry cases, 178,572 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90018701 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Spinal canal stenosis 661 East Asian ancestry cases, 178,065 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90018702 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Subarachnoid hemorrhage 1,203 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Illumina [13425781] (imputed) 1 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90018703 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Substance dependence 118 East Asian ancestry cases, 178,608 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90018704 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Type 1 diabetes 1,219 East Asian ancestry cases, 132,032 East Asian ancestry controls NA Illumina [13421694] (imputed) 3 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90018705 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Type 2 diabetes 45,383 East Asian ancestry cases, 132,032 East Asian ancestry controls NA Illumina [13429769] (imputed) 104 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90018706 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Stevens-Johnson syndrome 93 East Asian ancestry cases, 171,753 East Asian ancestry controls NA Illumina [13429124] (imputed) 1 Stevens-Johnson syndrome http://www.ebi.ac.uk/efo/EFO_0004276 GCST90018707 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Tatto pigmentation 224 East Asian ancestry cases, 178,502 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90018708 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Thyroid cancer 361 East Asian ancestry cases, 178,362 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90018709 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Tonsillitis 420 East Asian ancestry cases, 151,846 East Asian ancestry controls NA Illumina [13425541] (imputed) 0 pharyngitis http://purl.obolibrary.org/obo/MONDO_0002258 GCST90018710 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Typhoid fever 257 East Asian ancestry cases, 178,071 East Asian ancestry controls NA Illumina [13429923] (imputed) 0 typhoid fever http://www.ebi.ac.uk/efo/EFO_0006789 GCST90018711 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Unstable angina pectoris 5,891 East Asian ancestry cases, 146,214 East Asian ancestry controls NA Illumina [13425416] (imputed) 13 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90018712 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hepatic cancer 2,122 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Illumina [13427386] (imputed) 4 liver neoplasm http://www.ebi.ac.uk/efo/EFO_1001513 GCST90018638 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Herpes infection 772 East Asian ancestry cases, 166,603 East Asian ancestry controls NA Illumina [13427944] (imputed) 0 Herpes simplex infection http://www.ebi.ac.uk/efo/EFO_1002022 GCST90018639 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hyperthyroidism 994 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Illumina [13429005] (imputed) 0 hyperthyroidism http://www.ebi.ac.uk/efo/EFO_0009189 GCST90018640 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hypertrophic cardiomyopathy 383 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Illumina [13429920] (imputed) 0 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST90018641 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hypothyroidism 1,114 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Illumina [13429045] (imputed) 7 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90018642 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Interstitial lung disease 1,046 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Illumina [13429875] (imputed) 3 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90018643 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ischemic stroke 22,664 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Illumina [13429439] (imputed) 5 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90018644 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Idiopathic thrombocytopenic purpura 168 East Asian ancestry cases, 178,558 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 autoimmune thrombocytopenic purpura http://www.ebi.ac.uk/efo/EFO_0007160 GCST90018645 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. IgA nephropathy 71 East Asian ancestry cases, 175,288 East Asian ancestry controls NA Illumina [13429474] (imputed) 0 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST90018646 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ileus 1,771 East Asian ancestry cases, 176,232 East Asian ancestry controls NA Illumina [13429884] (imputed) 0 ileus http://purl.obolibrary.org/obo/MONDO_0004567 GCST90018647 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Inguinal hernia 1,664 East Asian ancestry cases, 177,062 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90018648 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Insomnia 389 East Asian ancestry cases, 177,864 East Asian ancestry controls NA Illumina [13429894] (imputed) 1 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST90018649 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Intracerebral hemorrhage 1,456 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Illumina [13425819] (imputed) 1 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90018650 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Iritis 110 East Asian ancestry cases, 175,543 East Asian ancestry controls NA Illumina [13429677] (imputed) 2 iritis http://www.ebi.ac.uk/efo/EFO_1000997 GCST90018651 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Iron deficiency anemia 4,618 East Asian ancestry cases, 174,057 East Asian ancestry controls NA Illumina [13429953] (imputed) 1 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90018652 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Juvenile rheumatoid arthritis 110 East Asian ancestry cases, 173,268 East Asian ancestry controls NA Illumina [13429185] (imputed) 0 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST90018653 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Keloid 1,055 East Asian ancestry cases, 177,671 East Asian ancestry controls NA Illumina [13429980] (imputed) 4 Keloid http://www.ebi.ac.uk/efo/EFO_0004212 GCST90018654 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Lung cancer 4,444 East Asian ancestry cases, 174,282 East Asian ancestry controls NA Illumina [13429980] (imputed) 8 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90018655 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Myasthenia gravis 81 East Asian ancestry cases, 178,630 East Asian ancestry controls NA Illumina [13429979] (imputed) 0 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST90018656 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Myocardial infarction 14,992 East Asian ancestry cases, 146,214 East Asian ancestry controls NA Illumina [13427135] (imputed) 39 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90018657 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Malignant lymphoma 335 East Asian ancestry cases, 177,342 East Asian ancestry controls NA Illumina [13429812] (imputed) 1 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90018658 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mastopathy 575 East Asian ancestry cases, 82,186 East Asian ancestry controls NA Illumina [13403071] (imputed) 0 breast fibrocystic disease http://www.ebi.ac.uk/efo/EFO_0003014 GCST90018659 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Meniere's disease 1,290 East Asian ancestry cases, 177,436 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90018660 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Metal allergy 278 East Asian ancestry cases, 161,777 East Asian ancestry controls NA Illumina [13427091] (imputed) 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90018661 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Myocarditis 102 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Illumina [13429830] (imputed) 0 myocarditis http://www.ebi.ac.uk/efo/EFO_0009609 GCST90018662 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Nasal polyps 160 East Asian ancestry cases, 151,846 East Asian ancestry controls NA Illumina [13425583] (imputed) 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90018663 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Nephrotic syndrome 1,314 East Asian ancestry cases, 177,412 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90018664 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Neuropathic bladder 308 East Asian ancestry cases, 178,418 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90018665 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Non-tuberculous mycobacterial infection 64 East Asian ancestry cases, 172,320 East Asian ancestry controls NA Illumina [13428847] (imputed) 0 Mycobacterium infection http://www.ebi.ac.uk/efo/EFO_0009429 GCST90018666 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Osteoporosis 9,794 East Asian ancestry cases, 168,932 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90018667 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ovarian cancer 843 East Asian ancestry cases, 60,614 East Asian ancestry controls NA Illumina [13381302] (imputed) 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90018668 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ovarian cyst 2,896 East Asian ancestry cases, 79,865 East Asian ancestry controls NA Illumina [13403071] (imputed) 0 Ovarian cyst http://purl.obolibrary.org/obo/HP_0000138 GCST90018669 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Peripheral artery disease 4,112 East Asian ancestry cases, 173,601 East Asian ancestry controls NA Illumina [13429824] (imputed) 3 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90018670 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Polymyositis 58 East Asian ancestry cases, 175,599 East Asian ancestry controls NA Illumina [13429616] (imputed) 1 polymyositis http://www.ebi.ac.uk/efo/EFO_0003063 GCST90018671 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pulmonary tuberculosis 7,800 East Asian ancestry cases, 170,871 East Asian ancestry controls NA Illumina [13429952] (imputed) 1 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90018672 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pancreatic cancer 499 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Illumina [13427108] (imputed) 1 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90018673 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Parkinson's disease 340 East Asian ancestry cases, 175,788 East Asian ancestry controls NA Illumina [13429429] (imputed) 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90018674 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pediatric asthma 547 East Asian ancestry cases, 161,803 East Asian ancestry controls NA Illumina [13427081] (imputed) 0 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90018675 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pericarditis 89 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Illumina [13429854] (imputed) 0 pericarditis http://www.ebi.ac.uk/efo/EFO_0007427 GCST90018676 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Periodontal disease 9,560 East Asian ancestry cases, 169,166 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90018677 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pharyngeal and laryngeal cancer 300 East Asian ancestry cases, 178,426 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 pharynx cancer, laryngeal carcinoma http://www.ebi.ac.uk/efo/EFO_0005577, http://purl.obolibrary.org/obo/MONDO_0002358 GCST90018678 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pleurisy 541 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Illumina [13429832] (imputed) 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90018679 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pneumoconiosis 85 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Illumina [13429760] (imputed) 0 pneumoconiosis http://purl.obolibrary.org/obo/MONDO_0015926 GCST90018680 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pneumonia 7,423 East Asian ancestry cases, 171,303 East Asian ancestry controls NA Illumina [13429980] (imputed) 2 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90018681 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pneumothorax 692 East Asian ancestry cases, 176,298 East Asian ancestry controls NA Illumina [13429753] (imputed) 0 pneumothorax http://purl.obolibrary.org/obo/MONDO_0002076 GCST90018682 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pollinosis 18,593 East Asian ancestry cases, 153,666 East Asian ancestry controls NA Illumina [13429010] (imputed) 4 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90018683 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Polycystic kidney disease 510 East Asian ancestry cases, 178,216 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 Polycystic Kidney Disease http://www.ebi.ac.uk/efo/EFO_0008620 GCST90018684 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Prostate cancer 5,672 East Asian ancestry cases, 84,660 East Asian ancestry controls NA Illumina [13406905] (imputed) 23 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90018685 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Preeclampsia 123 East Asian ancestry cases, 81,962 East Asian ancestry controls NA Illumina [13402395] (imputed) 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90018686 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Psoriasis vulgaris 206 East Asian ancestry cases, 172,289 East Asian ancestry controls NA Illumina [13429050] (imputed) 1 psoriasis vulgaris http://www.ebi.ac.uk/efo/EFO_1001494 GCST90018687 Genome-wide genotyping array 2022-10-24 34572589 Lin CL 2021-09-17 Biomolecules www.ncbi.nlm.nih.gov/pubmed/34572589 The Aldehyde Dehydrogenase ALDH2*2 Allele, Associated with Alcohol Drinking Behavior, Dates Back to Prehistoric Times. Hazardous alcohol drinking 71 East Asian ancestry cases, 126 East Asian ancestry controls NA Affymetrix [750000] 7 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90044901 Genome-wide genotyping array 2022-08-16 35627254 Mansachs SJ 2022-05-12 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35627254 Genetic Variants Associated with Neuropeptide Y Autoantibody Levels in Newly Diagnosed Individuals with Type 1 Diabetes. Neuropeptide Y autoantibody levels in type 1 diabetes 546 European ancestry children NA Illumina [3119616] (imputed) 10 autoantibody measurement http://www.ebi.ac.uk/efo/EFO_0004866 GCST90132189 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Word reading 27,180 European ancestry individuals, 1,238 Hispanic or African American individuals, 5,541 individuals NA Affymetrix, Illumina [9098670] (imputed) 71 word reading http://www.ebi.ac.uk/efo/EFO_0005300 GCST90104462 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Word reading 27,180 European ancestry individuals NA Affymetrix, Illumina [8014491] (imputed) 0 word reading http://www.ebi.ac.uk/efo/EFO_0005300 GCST90104463 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Non-word reading 16,746 European ancestry individuals, 1,238 Hispanic or African American individuals NA Affymetrix, Illumina [7879520] (imputed) 18 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST90104464 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Non-word reading 16,746 European ancestry individuals NA Affymetrix, Illumina [7854666] (imputed) 0 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST90104465 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Spelling 17,278 European ancestry individuals, 1,236 Hispanic or African American individuals NA Affymetrix, Illumina [7849740] (imputed) 6 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST90104466 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Spelling 17,278 European ancestry individuals NA Affymetrix, Illumina [7829087] (imputed) 0 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST90104467 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Phoneme awareness 12,411 European ancestry individuals, 1,222 Hispanic or African American individuals NA Affymetrix, Illumina [7798912] (imputed) 58 phoneme awareness http://www.ebi.ac.uk/efo/EFO_0021812 GCST90104468 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Phoneme awareness 12,411 European ancestry individuals NA Affymetrix, Illumina [7773752] (imputed) 0 phoneme awareness http://www.ebi.ac.uk/efo/EFO_0021812 GCST90104469 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Non-word repetition 12,828 European ancestry individuals, 1,218 individuals NA Affymetrix, Illumina [7862424] (imputed) 2 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST90104470 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Non-word repetition 12,828 European ancestry individuals NA Affymetrix, Illumina [7798762] (imputed) 0 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST90104471 Genome-wide genotyping array 2022-09-06 35998220 Eising E 2022-08-23 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35998220 Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people. Performance intelligence quotient 18,722 European ancestry individuals NA Affymetrix, Illumina [7872714] (imputed) 6 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST90104472 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/14:0) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Sterol ester (27:1/14:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045188 GCST90277238 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/15:0) levels 6,428 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Sterol ester (27:1/15:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045189 GCST90277239 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/16:0) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 9 level of Sterol ester (27:1/16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045191 GCST90277240 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/16:1) levels 7,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Sterol ester (27:1/16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045190 GCST90277241 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/17:0) levels 7,047 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Sterol ester (27:1/17:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045192 GCST90277242 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/17:1) levels 7,166 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90277243 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/18:0) levels 7,157 Finnish ancestry individuals NA Illumina [11318730] (imputed) 9 level of Sterol ester (27:1/18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045196 GCST90277244 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/18:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Sterol ester (27:1/18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045195 GCST90277245 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/18:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 7 level of Sterol ester (27:1/18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045194 GCST90277246 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/18:3) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Sterol ester (27:1/18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045193 GCST90277247 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/20:2) levels 5,848 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Sterol ester (27:1/20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045200 GCST90277248 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/20:3) levels 7,171 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Sterol ester (27:1/20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045199 GCST90277249 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/20:4) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 8 level of Sterol ester (27:1/20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045198 GCST90277250 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/20:5) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Sterol ester (27:1/20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045197 GCST90277251 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sterol ester (27:1/22:6) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Sterol ester (27:1/22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045201 GCST90277252 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Ceramide (d40:1) levels 7,117 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Ceramide (d40:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045185 GCST90277253 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Ceramide (d40:2) levels 5,287 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Ceramide (d40:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045184 GCST90277254 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Ceramide (d42:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Ceramide (d42:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045187 GCST90277255 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Ceramide (d42:2) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Ceramide (d42:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045186 GCST90277256 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Cholesterol levels 7,166 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90277257 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Diacylglycerol (16:0_18:1) levels 6,293 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Diacylglycerol (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045167 GCST90277258 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Diacylglycerol (16:0_18:2) levels 6,075 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Diacylglycerol (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045168 GCST90277259 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Diacylglycerol (16:1_18:1) levels 6,215 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Diacylglycerol (16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045169 GCST90277260 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Diacylglycerol (18:1_18:1) levels 6,884 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Diacylglycerol (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045170 GCST90277261 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Diacylglycerol (18:1_18:2) levels 6,613 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Diacylglycerol (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045171 GCST90277262 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:1_18:2) levels 6,718 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (O-18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045129 GCST90277338 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:1_20:3) levels 6,836 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-18:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045130 GCST90277339 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:1_20:4) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (O-18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045131 GCST90277340 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:2_16:0) levels 7,158 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (O-18:2_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045132 GCST90277341 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:2_18:1) levels 6,677 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (O-18:2_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045133 GCST90277342 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:2_18:2) levels 7,153 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045134 GCST90277343 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:2_20:4) levels 6,127 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045135 GCST90277344 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (16:0_18:2) levels 5,462 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylethanolamine (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045136 GCST90277345 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (16:0_20:4) levels 6,666 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylethanolamine (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045137 GCST90277346 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (18:0_18:2) levels 7,128 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Phosphatidylethanolamine (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045139 GCST90277347 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (18:0_20:4) levels 7,164 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylethanolamine (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045140 GCST90277348 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (18:1_18:1) levels 7,045 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylethanolamine (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045142 GCST90277349 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-16:1_18:2) levels 5,430 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylethanolamine (O-16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045144 GCST90277350 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-16:1_20:4) levels 7,169 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylethanolamine (O-16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045145 GCST90277351 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-16:1_22:5) levels 5,609 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylethanolamine (O-16:1_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045146 GCST90277352 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-18:1_18:2) levels 6,870 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylethanolamine (O-18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045147 GCST90277353 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-18:1_20:4) levels 7,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylethanolamine (O-18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045148 GCST90277354 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-18:2_18:1) levels 6,717 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylethanolamine (O-18:2_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045149 GCST90277355 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-18:2_18:2) levels 6,337 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylethanolamine (O-18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045150 GCST90277356 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (O-18:2_20:4) levels 7,154 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylethanolamine (O-18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045151 GCST90277357 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (16:0_18:1) levels 7,157 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylinositol (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045152 GCST90277358 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (16:0_18:2) levels 6,998 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylinositol (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045153 GCST90277359 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (16:0_20:4) levels 5,519 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylinositol (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045154 GCST90277360 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (18:0_18:1) levels 7,162 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Phosphatidylinositol (18:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045155 GCST90277361 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (18:0_18:2) levels 7,170 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Phosphatidylinositol (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045156 GCST90277362 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_20:5) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (16:0_20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045077 GCST90277288 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_22:4) levels 6,874 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (16:0_22:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045078 GCST90277289 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_22:5) levels 7,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (16:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045079 GCST90277290 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_22:6) levels 7,170 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (16:0_22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045080 GCST90277291 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:1_18:0) levels 6,524 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (16:1_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045081 GCST90277292 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:1_18:1) levels 7,166 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Phosphatidylcholine (16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045082 GCST90277293 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:1_18:2) levels 7,165 Finnish ancestry individuals NA Illumina [11318730] (imputed) 7 level of Phosphatidylcholine (16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045083 GCST90277294 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:1_20:4) levels 5,564 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045084 GCST90277295 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (17:0_18:1) levels 7,073 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (17:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045085 GCST90277296 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (17:0_18:2) levels 7,170 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (17:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045086 GCST90277297 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (17:0_20:4) levels 7,106 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (17:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045087 GCST90277298 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_18:1) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (18:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045089 GCST90277299 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_18:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylcholine (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045090 GCST90277300 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_18:3) levels 6,692 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (18:0_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045091 GCST90277301 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_20:2) levels 5,778 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (18:0_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045092 GCST90277302 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_20:3) levels 7,169 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (18:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045093 GCST90277303 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_20:4) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045094 GCST90277304 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_20:5) levels 7,121 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (18:0_20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045095 GCST90277305 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_22:5) levels 6,805 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (18:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045096 GCST90277306 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_22:6) levels 7,004 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (18:0_22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045097 GCST90277307 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:1_18:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylcholine (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045099 GCST90277308 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:1_18:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045100 GCST90277309 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:1_18:3) levels 6,339 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (18:1_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045101 GCST90277310 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:1_20:2) levels 5,852 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (18:1_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045102 GCST90277311 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:1_20:3) levels 7,171 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (18:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045103 GCST90277312 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:1_20:4) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045104 GCST90277313 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:2_18:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045106 GCST90277314 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:2_20:1) levels 5,521 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (18:2_20:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045107 GCST90277315 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:2_20:3) levels 6,615 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (18:2_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045108 GCST90277316 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:2_20:4) levels 7,049 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylcholine (18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045109 GCST90277317 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:0_16:0) levels 6,605 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (O-16:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045111 GCST90277318 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:0_16:1) levels 5,658 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-16:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045112 GCST90277319 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:0_18:1) levels 6,956 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045113 GCST90277320 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:0_18:2) levels 7,158 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045114 GCST90277321 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:0_20:3) levels 6,709 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (O-16:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045115 GCST90277322 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:0_20:4) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045116 GCST90277323 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:0_22:5) levels 5,988 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (O-16:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045117 GCST90277324 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:1_16:0) levels 5,868 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (O-16:1_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045118 GCST90277325 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:1_18:0) levels 6,751 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (O-16:1_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045119 GCST90277326 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:1_18:1) levels 7,154 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (O-16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045120 GCST90277327 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:1_18:2) levels 7,096 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045121 GCST90277328 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:1_20:3) levels 6,770 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (O-16:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045122 GCST90277329 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:1_20:4) levels 6,025 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (O-16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045123 GCST90277330 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-16:2_18:0) levels 6,672 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90277331 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-17:0_15:0) levels 6,140 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (O-17:0_15:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045124 GCST90277332 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-17:0_17:1) levels 6,880 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90277333 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:0_14:0) levels 6,462 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (O-18:0_14:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045125 GCST90277334 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:0_16:1) levels 5,959 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (O-18:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045126 GCST90277335 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:0_20:4) levels 6,956 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (O-18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045127 GCST90277336 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (O-18:1_16:0) levels 6,956 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (O-18:1_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045128 GCST90277337 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Kidney disese (macroalbuminuria or end-stage renal disease) in diabetes 6,705 European ancestry cases, 15,430 European ancestry controls NA Illumina [NR] (imputed) 2 albuminuria, stage 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0004285, http://www.ebi.ac.uk/efo/EFO_0009909 GCST90134331 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Macroalbuminuria in diabetes 3,528 European ancestry cases, 14,448 European ancestry controls NA Illumina [NR] (imputed) 0 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST90134332 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. End-stage renal disease in diabetes 2,717 European ancestry cases, 14,962 European ancestry controls NA Illumina [NR] (imputed) 1 stage 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0009909 GCST90134333 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. End-stage renal disease in diabetes 2,717 European ancestry cases, 22,924 European ancestry controls NA Illumina [NR] (imputed) 1 stage 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0009909 GCST90134334 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Kidney disease (end stage renal disease vs macroalbuminuria) in diabetes 2,640 European ancestry cases, 3,502 European ancestry controls NA Illumina [NR] (imputed) 1 albuminuria, stage 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0004285, http://www.ebi.ac.uk/efo/EFO_0009909 GCST90134335 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Kidney disease (end stage renal disease or macroalbuminuria or microalbuminuria) in diabetes 11,380 European ancestry cases, 15,405 European ancestry controls NA Illumina [NR] (imputed) 1 albuminuria, Moderate albuminuria, stage 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0004285, http://purl.obolibrary.org/obo/HP_0012594, http://www.ebi.ac.uk/efo/EFO_0009909 GCST90134336 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Microalbuminuria in diabetes 4,779 European ancestry cases, 15,331 European ancestry controls NA Illumina [NR] (imputed) 3 Moderate albuminuria http://purl.obolibrary.org/obo/HP_0012594 GCST90134337 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Reduced eGFR in diabetes 7,636 European ancestry cases, 18,576 European ancestry controls NA Illumina [NR] (imputed) 2 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90134338 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Chronic kidney disease (reduced eGFR or end stage renal disease) in diabetes 2,660 European ancestry cases, 18,163 European ancestry controls NA Illumina [NR] (imputed) 0 glomerular filtration rate, stage 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0009909 GCST90134339 Genome-wide genotyping array 2022-09-02 35763030 Sandholm N 2022-06-28 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35763030 Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease. Kidney disease (reduced eGFR and albuminuria or end stage renal disease) in diabetes 4,122 European ancestry cases, 13,972 European ancestry controls NA Illumina [NR] (imputed) 2 albuminuria, glomerular filtration rate, stage 5 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0004285, http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0009909 GCST90134340 Genome-wide genotyping array 2022-09-22 35956399 Hur HJ 2022-08-06 Nutrients www.ncbi.nlm.nih.gov/pubmed/35956399 Association of Polygenic Variants with Type 2 Diabetes Risk and Their Interaction with Lifestyles in Asians. Type 2 diabetes 5,383 Korean ancestry cases, 53,318 Korean ancestry controls East Asian ancestry individuals Affymetrix [NR] (imputed) 4 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90137502 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Atrial fibrillation/atrial flutter 4,150 East Asian ancestry cases, 155,540 East Asian ancestry controls NA Illumina [13427194] (imputed) 8 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90018576 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic bronchitis 271 East Asian ancestry cases, 161,803 East Asian ancestry controls NA Illumina [13427039] (imputed) 1 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST90018604 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic gastritis 744 East Asian ancestry cases, 177,982 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 chronic gastritis http://www.ebi.ac.uk/efo/EFO_0000337 GCST90018605 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cirrhosis 2,551 East Asian ancestry cases, 176,175 East Asian ancestry controls NA Illumina [13429980] (imputed) 5 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90018606 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Colon polyp 4,768 East Asian ancestry cases, 166,052 East Asian ancestry controls NA Illumina [13428894] (imputed) 1 polyp of colon http://purl.obolibrary.org/obo/MONDO_0021400 GCST90018607 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Compression fracture 2,856 East Asian ancestry cases, 175,870 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90018608 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Constipation 397 East Asian ancestry cases, 176,232 East Asian ancestry controls NA Illumina [13429711] (imputed) 0 Constipation http://purl.obolibrary.org/obo/HP_0002019 GCST90018609 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Contact dermatitis 247 East Asian ancestry cases, 161,777 East Asian ancestry controls NA Illumina [13427082] (imputed) 0 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90018610 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cystitis 1,665 East Asian ancestry cases, 175,288 East Asian ancestry controls NA Illumina [13429618] (imputed) 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90018611 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Diabetic nephropathy 220 East Asian ancestry cases, 132,764 East Asian ancestry controls NA Illumina [13421642] (imputed) 0 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90018612 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Depression 836 East Asian ancestry cases, 177,794 East Asian ancestry controls NA Illumina [13429968] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90018613 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Dilated cardiomyopathy 417 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Illumina [13429894] (imputed) 0 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST90018614 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Aortic aneurysm 1,155 East Asian ancestry cases, 173,601 East Asian ancestry controls NA Illumina [13429364] (imputed) 0 aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0001666 GCST90018563 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Atopic dermatitis 4,296 East Asian ancestry cases, 163,807 East Asian ancestry controls NA Illumina [13428180] (imputed) 16 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90018564 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Bronchiectasis 241 East Asian ancestry cases, 161,803 East Asian ancestry controls NA Illumina [13427077] (imputed) 1 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90018581 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Bronchitis 1,465 East Asian ancestry cases, 170,000 East Asian ancestry controls NA Illumina [13428877] (imputed) 2 bronchitis http://www.ebi.ac.uk/efo/EFO_0009661 GCST90018582 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hepatic bile duct cancer 418 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Illumina [13427010] (imputed) 0 cholangiocarcinoma http://www.ebi.ac.uk/efo/EFO_0005221 GCST90018583 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic hepatitis B infection 2,234 East Asian ancestry cases, 169,588 East Asian ancestry controls NA Illumina [13428705] (imputed) 1 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST90018584 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute renal failure 465 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Illumina [13429317] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90018570 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Allergic conjunctivitis 3,900 East Asian ancestry cases, 174,719 East Asian ancestry controls NA Illumina [13429967] (imputed) 0 conjunctivitis http://www.ebi.ac.uk/efo/EFO_0009450 GCST90018571 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Allergic rhinitis 7,897 East Asian ancestry cases, 153,666 East Asian ancestry controls NA Illumina [13427369] (imputed) 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90018572 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Angina pectoris 14,007 East Asian ancestry cases, 145,158 East Asian ancestry controls NA Illumina [13426705] (imputed) 19 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90018573 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Aplastic anemia 53 East Asian ancestry cases, 174,057 East Asian ancestry controls NA Illumina [13429217] (imputed) 1 Aplastic anemia http://purl.obolibrary.org/obo/HP_0001915 GCST90018574 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Colorectal cancer 8,305 East Asian ancestry cases, 159,386 East Asian ancestry controls NA Illumina [13428297] (imputed) 14 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90018588 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic suppurative otitis media 2,206 East Asian ancestry cases, 176,520 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 suppurative otitis media http://www.ebi.ac.uk/efo/EFO_0007503 GCST90018589 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cesarian section 451 East Asian ancestry cases, 82,310 East Asian ancestry controls NA Illumina [13403071] (imputed) 0 cesarean section http://www.ebi.ac.uk/efo/EFO_0009636 GCST90018590 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cardiac valvular disease 1,995 East Asian ancestry cases, 176,731 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 heart valve disease http://www.ebi.ac.uk/efo/EFO_0009551 GCST90018591 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic pancreatitis 457 East Asian ancestry cases, 177,471 East Asian ancestry controls NA Illumina [13429808] (imputed) 1 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90018601 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic renal failure 2,117 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Illumina [13429586] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90018602 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Diphtheria 541 East Asian ancestry cases, 170,247 East Asian ancestry controls NA Illumina [13428661] (imputed) 0 diphtheria http://www.ebi.ac.uk/efo/EFO_0005549 GCST90018615 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Dysentery 411 East Asian ancestry cases, 178,071 East Asian ancestry controls NA Illumina [13429933] (imputed) 1 dysentery http://www.ebi.ac.uk/efo/EFO_1001869 GCST90018616 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ectopic pregnancy 605 East Asian ancestry cases, 82,156 East Asian ancestry controls NA Illumina [13403071] (imputed) 0 Ectopic pregnancy http://purl.obolibrary.org/obo/HP_0031456 GCST90018617 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Endometrial cancer 1,200 East Asian ancestry cases, 60,614 East Asian ancestry controls NA Illumina [13381748] (imputed) 0 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST90018618 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Endometriosis 1,786 East Asian ancestry cases, 80,975 East Asian ancestry controls NA Illumina [13403071] (imputed) 2 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90018619 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Epilepsy 2,466 East Asian ancestry cases, 175,788 East Asian ancestry controls NA Illumina [13429903] (imputed) 1 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90018620 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Esophageal cancer 1,388 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Illumina [13427188] (imputed) 4 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST90018621 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Esophageal varix 264 East Asian ancestry cases, 177,516 East Asian ancestry controls NA Illumina [13429790] (imputed) 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90018622 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Bell's palsy 343 East Asian ancestry cases, 178,191 East Asian ancestry controls NA Illumina [13429851] (imputed) 0 Bell's palsy http://www.ebi.ac.uk/efo/EFO_0007167 GCST90018623 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Febrile seizures 574 East Asian ancestry cases, 175,272 East Asian ancestry controls NA Illumina [13429256] (imputed) 0 Seizure http://purl.obolibrary.org/obo/HP_0001250 GCST90018624 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Food allergy 3,777 East Asian ancestry cases, 165,939 East Asian ancestry controls NA Illumina [13428657] (imputed) 0 food allergy measurement http://www.ebi.ac.uk/efo/EFO_0007016 GCST90018625 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gallbladder polyp 843 East Asian ancestry cases, 167,459 East Asian ancestry controls NA Illumina [13133316] (imputed) 1 polyp of gallbladder http://purl.obolibrary.org/obo/MONDO_0021416 GCST90018626 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Graves' disease 2,809 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Illumina [13429311] (imputed) 15 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST90018627 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastroesophageal reflux disease 948 East Asian ancestry cases, 177,516 East Asian ancestry controls NA Illumina [13429914] (imputed) 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90018628 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastric cancer 7,921 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Illumina [13428249] (imputed) 7 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90018629 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastric polyp 1,337 East Asian ancestry cases, 158,249 East Asian ancestry controls NA Illumina [13427015] (imputed) 2 stomach polyp http://purl.obolibrary.org/obo/MONDO_0008277 GCST90018630 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastric ulcer 12,650 East Asian ancestry cases, 161,227 East Asian ancestry controls NA Illumina [13429311] (imputed) 4 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90018631 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Glaucoma 8,448 East Asian ancestry cases, 168,903 East Asian ancestry controls NA Illumina [13429686] (imputed) 8 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90018632 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Goiter 1,127 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Illumina [13429016] (imputed) 0 goiter http://www.ebi.ac.uk/efo/EFO_0004283 GCST90018633 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute hepatitis A infection 261 East Asian ancestry cases, 166,603 East Asian ancestry controls NA Illumina [13427866] (imputed) 0 hepatitis A virus infection http://www.ebi.ac.uk/efo/EFO_0007305 GCST90018634 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hashimoto thyroiditis 537 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Illumina [13428945] (imputed) 2 Hashimoto's thyroiditis http://www.ebi.ac.uk/efo/EFO_0003779 GCST90018635 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Head injury 2,440 East Asian ancestry cases, 176,286 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90018636 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hearing loss, difficulty in hearing 3,400 East Asian ancestry cases, 175,326 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90018637 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic sinusitis 4,617 East Asian ancestry cases, 152,226 East Asian ancestry controls NA Illumina [13426486] (imputed) 5 chronic rhinosinusitis http://www.ebi.ac.uk/efo/EFO_1000024 GCST90018603 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Back pain 1,732 East Asian ancestry cases, 176,994 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90018577 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Behcet's disease 78 East Asian ancestry cases, 171,966 East Asian ancestry controls NA Illumina [13428939] (imputed) 0 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST90018578 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Breast cancer 6,325 East Asian ancestry cases, 73,225 East Asian ancestry controls NA Illumina [13401000] (imputed) 8 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90018579 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Brain tumor 405 East Asian ancestry cases, 178,321 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90018580 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Autoimmune hepatitis 85 East Asian ancestry cases, 166,529 East Asian ancestry controls NA Illumina [13427809] (imputed) 1 Autoimmune Hepatitis http://www.ebi.ac.uk/efo/EFO_0005676 GCST90018565 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Abortion 136 East Asian ancestry cases, 82,625 East Asian ancestry controls NA Illumina [13403071] (imputed) 0 abortion http://www.ebi.ac.uk/efo/EFO_1001491 GCST90018566 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Achilles tendon injury 312 East Asian ancestry cases, 175,979 East Asian ancestry controls NA Illumina [13429681] (imputed) 0 Tendinopathy http://www.ebi.ac.uk/efo/EFO_1001434 GCST90018567 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute glomerulonephritis 443 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Illumina [13429216] (imputed) 0 glomerulonephritis http://purl.obolibrary.org/obo/MONDO_0002462 GCST90018568 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute pancreatitis 827 East Asian ancestry cases, 177,471 East Asian ancestry controls NA Illumina [13429917] (imputed) 1 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90018569 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic hepatitis C infection 7,110 East Asian ancestry cases, 169,588 East Asian ancestry controls NA Illumina [13429570] (imputed) 4 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST90018585 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic heart failure 10,540 East Asian ancestry cases, 168,186 East Asian ancestry controls NA Illumina [13429980] (imputed) 3 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90018586 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic obstructive pulmonary disease 4,017 East Asian ancestry cases, 162,653 East Asian ancestry controls NA Illumina [13427899] (imputed) 5 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90018587 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Asthma 13,015 East Asian ancestry cases, 162,933 East Asian ancestry controls NA Illumina [13429513] (imputed) 21 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90018575 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cardiomegaly 743 East Asian ancestry cases, 177,983 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 cardiac hypertrophy http://www.ebi.ac.uk/efo/EFO_0002503 GCST90018592 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Carpal tunnel syndrome 192 East Asian ancestry cases, 178,534 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90018593 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cataracts 38,194 East Asian ancestry cases, 140,532 East Asian ancestry controls NA Illumina [13429980] (imputed) 2 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90018594 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cerebral aneurysm 3,132 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Illumina [13426064] (imputed) 4 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90018595 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Unruptured cerebral aneurysm 91 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Illumina [13425573] (imputed) 1 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90018596 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cervical cancer 967 East Asian ancestry cases, 60,614 East Asian ancestry controls NA Illumina [13381745] (imputed) 2 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90018597 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cholecystitis 1,860 East Asian ancestry cases, 168,253 East Asian ancestry controls NA Illumina [13428642] (imputed) 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90018598 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cholelithiasis 9,305 East Asian ancestry cases, 168,253 East Asian ancestry controls NA Illumina [13429768] (imputed) 15 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90018599 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic glomerulonephritis 210 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Illumina [13429313] (imputed) 0 glomerulonephritis http://purl.obolibrary.org/obo/MONDO_0002462 GCST90018600 Genome-wide genotyping array 2022-04-26 34982113 Liao C 2022-01-04 JAMA Neurol www.ncbi.nlm.nih.gov/pubmed/34982113 Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis. Essential tremor 7,177 European ancestry cases, 475,877 European ancestry controls NA Affymetrix, Illumina [6892661] (imputed) 85 essential tremor http://www.ebi.ac.uk/efo/EFO_0003108 GCST90101814 Genome-wide genotyping array 2022-08-18 35616254 Li C 2022-05-26 Mov Disord www.ncbi.nlm.nih.gov/pubmed/35616254 Genetic Determinants of Survival in Parkinson's Disease in the Asian Population. Mortality in Parkinson's disease 85 Chinese ancestry cases, 995 Chinese ancestry controls NA Illumina [NR] (imputed) 1 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST90132301 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Height 59,771 Hispanic or Latin American individuals 8,110 Hispanic or Latin American individuals Affymetrix, Illumina [8927938] (imputed) 116 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90095033 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Body mass index 56,161 Hispanic or Latin American individuals 10,538 Hispanic or Latin American individuals Affymetrix, Illumina [8827898] (imputed) 31 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90095034 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Waist-to-hip ratio adjusted for BMI 42,455 Hispanic or Latin American individuals 4,393 Hispanic or Latin American individuals Affymetrix, Illumina [8415721] (imputed) 7 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90095035 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Waist-to-hip ratio adjusted for BMI 13,500 Hispanic or Latin American men up to 1,646 Hispanic or Latin American men Affymetrix, Illumina [8015711] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90095036 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Waist-to-hip ratio adjusted for BMI 28,955 Hispanic or Latin American women 2,747 Hispanic or Latin American women Affymetrix, Illumina [8227392] (imputed) 7 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90095037 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Height 350,741 Hispanic or Latin American, African or European ancestry individuals 1,945 Hispanic or Latin American children/adolescents, 336,474 British ancestry individuals Affymetrix, Illumina [2427315] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90095038 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Body mass index 330,793 Hispanic or Latin American, African or European ancestry individuals 1,914 Hispanic or Latin American children/adolescents, 336,107 British ancestry individuals Affymetrix, Illumina [2427043] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90095039 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Waist-to-hip ratio adjusted for BMI 205,581 Hispanic or Latin American, African or European ancestry individuals 484,563 British ancestry individuals Affymetrix, Illumina [2401745] (imputed) 2 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90095040 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Waist-to-hip ratio adjusted for BMI 77,482 Hispanic or Latin American, African or European ancestry men NA Affymetrix, Illumina [2099213] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90095041 Genome-wide genotyping array 2022-04-26 35399580 Fernandez-Rhodes L 2022-03-11 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35399580 Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium. Waist-to-hip ratio adjusted for BMI 126,003 Hispanic or Latin American, African or European ancestry women NA Affymetrix, Illumina [2363453] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90095042 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid amyloid beta 42 levels 8,074 European ancestry individuals 5,042 individuals Illumina [9789766] (imputed) 5 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90129599 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid p-tau levels 7,798 European ancestry individuals 4,755 individuals Illumina [9782734] (imputed) 4 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90129600 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid amyloid beta 42 levels in abnormal amyloid levels 3,775 European ancestry individuals NA Illumina [NR] (imputed) 2 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90134626 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid amyloid beta 42 levels in APOE e4 non-carriers 3,201 European ancestry individuals NA Illumina [NR] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90134627 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid amyloid beta 42 levels in APOE e4 carriers 3,240 European ancestry individuals NA Illumina [NR] (imputed) 2 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90134628 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid amyloid beta 42 levels in normal amyloid levels 3,182 European ancestry individuals NA Illumina [NR] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90134629 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid p-tau levels in abnormal amyloid levels 3,534 European ancestry individuals NA Illumina [NR] (imputed) 1 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90134630 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid p-tau levels in APOE e4 non-carriers 3,141 European ancestry individuals NA Illumina [NR] (imputed) 1 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90134631 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid p-tau levels in APOE e4 carriers 3,047 European ancestry individuals NA Illumina [NR] (imputed) 1 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90134632 Genome-wide genotyping array 2022-09-14 36066633 Jansen IE 2022-09-06 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/36066633 Genome-wide meta-analysis for Alzheimer's disease cerebrospinal fluid biomarkers. Cerebrospinal fluid p-tau levels in normal amyloid levels 3,174 European ancestry individuals NA Illumina [NR] (imputed) 2 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90134633 Genome-wide genotyping array 2022-09-30 34391895 Kanai M 2021-08-12 Ann Oncol www.ncbi.nlm.nih.gov/pubmed/34391895 Large-Scale Prospective Genome-Wide Association Study of Oxaliplatin in Stage II/III Colon Cancer and Neuropathy. Oxaliplatin-induced peripheral sensory neuropathy in colon cancer 383 Japanese ancestry cases, 605 Japanese ancestry controls NA Illumina [6412903] (imputed) 7 sensory peripheral neuropathy, response to platinum based chemotherapy http://purl.obolibrary.org/obo/MONDO_0002321, http://www.ebi.ac.uk/efo/EFO_0004647 GCST90060085 Genome-wide genotyping array 2022-09-30 34391895 Kanai M 2021-08-12 Ann Oncol www.ncbi.nlm.nih.gov/pubmed/34391895 Large-Scale Prospective Genome-Wide Association Study of Oxaliplatin in Stage II/III Colon Cancer and Neuropathy. Oxaliplatin-induced peripheral sensory neuropathy in colon cancer (extreme) 233 Japanese ancestry cases, 49 Japanese ancestry controls NA Illumina [6412903] (imputed) 2 sensory peripheral neuropathy, response to platinum based chemotherapy http://purl.obolibrary.org/obo/MONDO_0002321, http://www.ebi.ac.uk/efo/EFO_0004647 GCST90060086 Genome-wide genotyping array 2022-09-30 34391895 Kanai M 2021-08-12 Ann Oncol www.ncbi.nlm.nih.gov/pubmed/34391895 Large-Scale Prospective Genome-Wide Association Study of Oxaliplatin in Stage II/III Colon Cancer and Neuropathy. Time to recovery from peripheral sensory neuropathy in colon cancer 1,364 Japanese ancestry individuals NA Illumina [6412903] (imputed) 13 sensory peripheral neuropathy, remission http://purl.obolibrary.org/obo/MONDO_0002321, http://www.ebi.ac.uk/efo/EFO_0009785 GCST90060087 Genome-wide genotyping array 2022-09-30 34391895 Kanai M 2021-08-12 Ann Oncol www.ncbi.nlm.nih.gov/pubmed/34391895 Large-Scale Prospective Genome-Wide Association Study of Oxaliplatin in Stage II/III Colon Cancer and Neuropathy. Oxaliplatin-induced allergic reactions in colon cancer 102 Japanese ancestry cases, 826 Japanese ancestry controls NA Illumina [6412903] (imputed) 19 response to platinum based chemotherapy, drug allergy http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0009482 GCST90060088 Genome-wide genotyping array 2022-09-30 34391895 Kanai M 2021-08-12 Ann Oncol www.ncbi.nlm.nih.gov/pubmed/34391895 Large-Scale Prospective Genome-Wide Association Study of Oxaliplatin in Stage II/III Colon Cancer and Neuropathy. Oxaliplatin-induced allergic reactions in colon cancer (extreme) 57 Japanese ancestry cases, 430 Japanese ancestry controls NA Illumina [6412903] (imputed) 6 response to platinum based chemotherapy, drug allergy http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0009482 GCST90060089 Genome-wide genotyping array 2022-09-30 34391895 Kanai M 2021-08-12 Ann Oncol www.ncbi.nlm.nih.gov/pubmed/34391895 Large-Scale Prospective Genome-Wide Association Study of Oxaliplatin in Stage II/III Colon Cancer and Neuropathy. Time to colon cancer recurrence 1,364 Japanese ancestry individuals NA Illumina [6412903] (imputed) 45 disease recurrence, colon carcinoma http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_1001950 GCST90060090 Genome-wide genotyping array 2022-09-23 36064556 Seviiri M 2022-09-05 J Transl Med www.ncbi.nlm.nih.gov/pubmed/36064556 Higher polygenic risk for melanoma is associated with improved survival in a high ultraviolet radiation setting. Melanoma specific survival 10,982 European ancestry individuals 1,947 European ancestry individuals Affymetrix [NR] (imputed) 2 survival time, melanoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000756 GCST90137504 Genome-wide genotyping array 2022-06-16 35313536 Yoo HY 2022-03-11 Clin Cosmet Investig Dermatol www.ncbi.nlm.nih.gov/pubmed/35313536 A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women. Facial skin melanin 730 Korean ancestry individuals NA Illumina [NR] (imputed) 13 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST90104590 Genome-wide genotyping array 2022-06-16 35313536 Yoo HY 2022-03-11 Clin Cosmet Investig Dermatol www.ncbi.nlm.nih.gov/pubmed/35313536 A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women. Facial skin gloss 730 Korean ancestry individuals NA Illumina [NR] (imputed) 13 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST90104591 Genome-wide genotyping array 2022-06-16 35313536 Yoo HY 2022-03-11 Clin Cosmet Investig Dermatol www.ncbi.nlm.nih.gov/pubmed/35313536 A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women. Facial skin hydration 730 Korean ancestry individuals NA Illumina [NR] (imputed) 15 skin hydration measurement http://www.ebi.ac.uk/efo/EFO_0009586 GCST90104592 Genome-wide genotyping array 2022-06-16 35313536 Yoo HY 2022-03-11 Clin Cosmet Investig Dermatol www.ncbi.nlm.nih.gov/pubmed/35313536 A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women. Facial wrinkles 730 Korean ancestry individuals NA Illumina [NR] (imputed) 16 facial morphology http://www.ebi.ac.uk/efo/EFO_0004743 GCST90104593 Genome-wide genotyping array 2022-06-16 35313536 Yoo HY 2022-03-11 Clin Cosmet Investig Dermatol www.ncbi.nlm.nih.gov/pubmed/35313536 A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women. Facial skin elasticity 730 Korean ancestry individuals NA Illumina [NR] (imputed) 16 facial morphology http://www.ebi.ac.uk/efo/EFO_0004743 GCST90104594 Genome-wide genotyping array 2022-08-04 35501119 Wang AL 2022-05-02 Thorax www.ncbi.nlm.nih.gov/pubmed/35501119 Novel genetic variants associated with inhaled corticosteroid treatment response in older adults with asthma. Oral corticosteroid burst in asthma 3,097 European ancestry cases, 2,613 European ancestry controls 503 European ancestry cases, 638 European ancestry controls Affymetrix [8995492] (imputed) 19 response to corticosteroid http://purl.obolibrary.org/obo/GO_0031960 GCST90131477 Genome-wide genotyping array 2022-08-04 35501119 Wang AL 2022-05-02 Thorax www.ncbi.nlm.nih.gov/pubmed/35501119 Novel genetic variants associated with inhaled corticosteroid treatment response in older adults with asthma. Asthma exacerbations in inhaled corticosteroid treatment 646 European ancestry cases, 3,895 European ancestry controls 202 European ancestry cases, 303 European ancestry controls Affymetrix [9004920] (imputed) 22 asthma exacerbation measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0007614, http://purl.obolibrary.org/obo/GO_0031960 GCST90131478 Genome-wide genotyping array 2023-02-22 34433106 Zhou JY 2021-07-21 Nutrition www.ncbi.nlm.nih.gov/pubmed/34433106 Regular exercise, alcohol consumption, and smoking interact with the polygenetic risk scores involved in insulin sensitivity and secretion for the risk of concurrent hyperglycemia, hypertension, and dyslipidemia. 3GO (hypertension, hyperglycemia and dyslipidemia) 570 Korean ancestry cases, 14,155 Korean ancestry controls NA Affymetrix [NR] 0 hypertension, Rare dyslipidemia, Hyperglycemia http://www.ebi.ac.uk/efo/EFO_0000537, http://www.orpha.net/ORDO/Orphanet_101953, http://purl.obolibrary.org/obo/HP_0003074 GCST90032675 Genome-wide genotyping array 2022-10-14 35879288 Chen Y 2022-07-25 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35879288 The interaction of early life factors and depression-associated loci affecting the age at onset of the depression. Age of onset of depression x felt loved as a child interaction 35,633 European ancestry individuals NA Affymetrix [NR] (imputed) 11 age of onset of depressive disorder, wellbeing measurement http://purl.obolibrary.org/obo/OBA_2040166, http://www.ebi.ac.uk/efo/EFO_0007869 GCST90132316 Genome-wide genotyping array 2022-08-31 35717853 Baranova A 2022-06-13 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/35717853 Shared genetics between autism spectrum disorder and attention-deficit/hyperactivity disorder and their association with extraversion. Attention deficit hyperactivity disorder or autism spectrum disorder (pleiotropy) 20,183 European ancestry ADHD cases, 35,191 European ancestry controls without ADHD, 18,381 European ancestry ASD cases, 27,969 European ancestry controls without ASD NA NR [NR] 3 attention deficit hyperactivity disorder, autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003756 GCST90133365 Genome-wide genotyping array 2022-08-19 35872910 Carcel-Marquez J 2022-07-08 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/35872910 A Polygenic Risk Score Based on a Cardioembolic Stroke Multitrait Analysis Improves a Clinical Prediction Model for This Stroke Subtype. Cardioembolic stroke (MTAG) 362,661 European ancestry individuals NA Illumina [6808676] (imputed) 44 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90132228 Genome-wide genotyping array 2022-08-19 35872910 Carcel-Marquez J 2022-07-08 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/35872910 A Polygenic Risk Score Based on a Cardioembolic Stroke Multitrait Analysis Improves a Clinical Prediction Model for This Stroke Subtype. Atrial fibrillation (MTAG) 1,030,836 European ancestry individuals NA Illumina [6808676] (imputed) 111 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90132229 Genome-wide genotyping array 2022-10-13 36124557 Chan MMY 2022-09-20 Elife www.ncbi.nlm.nih.gov/pubmed/36124557 Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves. Posterior urethral valves 89 European ancestry cases, 19,418 European ancestry controls, 18 South Asian ancestry cases, 2,847 South Asian ancestry controls, 11 African ancestry cases, 449 African ancestry controls, 7 Hispanic or Latin American controls, 14 Other admixed ancestry cases, 1,006 Other admixed ancestry controls NA Illumina [19651224] 4 posterior urethral valve http://purl.obolibrary.org/obo/MONDO_0019640 GCST90134254 Genome-wide sequencing 2022-10-13 36124557 Chan MMY 2022-09-20 Elife www.ncbi.nlm.nih.gov/pubmed/36124557 Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves. Posterior urethral valves 89 European ancestry cases, 19,418 European ancestry controls 395 European ancestry cases, 4,151 European ancestry controls Illumina [16938500] 1 posterior urethral valve http://purl.obolibrary.org/obo/MONDO_0019640 GCST90165183 Genome-wide sequencing 2022-10-06 35879306 Hou J 2022-07-25 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35879306 Polygenic resilience scores capture protective genetic effects for Alzheimer's disease. Late-onset Alzheimer's disease in high risk polygenic risk score 11,309 European ancestry cases, 2,263 European ancestry controls NA NR [94655] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90162599 Genome-wide genotyping array 2022-10-06 35879306 Hou J 2022-07-25 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35879306 Polygenic resilience scores capture protective genetic effects for Alzheimer's disease. Late-onset Alzheimer's disease in high risk polygenic risk score APOEe4 carriers 6,541 European ancestry cases, 988 European ancestry controls NA NR [86752] (imputed) 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90162600 Genome-wide genotyping array 2022-11-29 35023977 Yao Y 2022-01-06 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35023977 Genome-Wide Association Study and Genetic Correlation Scan Provide Insights into Its Genetic Architecture of Sleep Health Score in the UK Biobank Cohort. Sleep health score 336,463 European ancestry individuals NA NR [NR] (imputed) 22 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST90102455 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Bread type: Wholemeal or wholegrain (UKB data field 1448_3) 434,087 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132966 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Bread type: White vs wholemeal/wholegrain and brown (UKB data field 1448) 416,312 European ancestry individuals NA NR [NR] (imputed) 7 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132967 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Bread type: Wholemeal/wholegrain vs white and brown (UKB data field 1448) 416,312 European ancestry individuals NA NR [NR] (imputed) 4 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132968 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cereal type: Biscuit cereal (e.g. Weetabix) (UKB data field 1468_2) 373,443 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132969 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cereal type: Bran cereal (e.g. All Bran, Branflakes) (UKB data field 1468_1) 373,443 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132970 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cereal type: Oat cereal (e.g. Ready Brek, porridge) (UKB data field 1468_3) 373,443 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132971 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cereal type: Muesli (UKB data field 1468_4) 373,443 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132972 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cereal type: Other (e.g. Cornflakes, Frosties) (UKB data field 1468_5) 373,443 European ancestry individuals NA NR [NR] (imputed) 6 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132973 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Bread consumption (slices per week) (UKB data field 1438) 444,230 European ancestry individuals NA NR [NR] (imputed) 16 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132981 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cereal consumption (bowls per week) (UKB data field 1458) 447,935 European ancestry individuals NA NR [NR] (imputed) 21 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132982 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Tea intake (UKB data field 1488) 448,060 European ancestry individuals NA NR [NR] (imputed) 29 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST90132983 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Coffee consumption (cups per day) 448,204 European ancestry individuals NA NR [NR] (imputed) 23 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90132984 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Water consumption (glasses per day) (UKB data field 1528) 445,965 European ancestry individuals NA NR [NR] (imputed) 34 beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010088 GCST90132985 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Champagne or white wine consumption (glasses per month) (UKB data field 1578, 4418) 387,404 European ancestry individuals NA NR [NR] (imputed) 7 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90132986 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Red wine consumption (glasses per month) (UKB data field 1578, 4419) 387,404 European ancestry individuals NA NR [NR] (imputed) 5 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90132987 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Beer or cider consumption (glasses per month) (UKB data field 1578, 4420) 387,404 European ancestry individuals NA NR [NR] (imputed) 9 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90132988 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spirits consumption (measures per month) (UKB data field 1578, 4421) 387,404 European ancestry individuals NA NR [NR] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90132989 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Fortified wine consumption (glasses per month) (UKB data field 1578, 4422) 387,404 European ancestry individuals NA NR [NR] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90132990 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Other alcohol consumption (glasses per month) (UKB data field 1578, 4423) 186,160 European ancestry individuals NA NR [NR] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90132991 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Alcohol consumption (drinks per month) (UKB data field 1578, 4424) 449,210 European ancestry individuals NA NR [NR] (imputed) 43 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90132992 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Oily fish consumption 446,854 European ancestry individuals NA NR [NR] (imputed) 37 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST90132993 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Non-oily fish consumption 447,289 European ancestry individuals NA NR [NR] (imputed) 2 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST90132994 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Processed meat consumption 448,303 European ancestry individuals NA NR [NR] (imputed) 8 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132995 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Poultry consumption 448,210 European ancestry individuals NA NR [NR] (imputed) 3 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132996 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Beef consumption (UKB data field 1369) 447,441 European ancestry individuals NA NR [NR] (imputed) 5 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132997 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Coffee type: Decaffeinated coffee (any type) (UKB data field 1508_1) 353,710 European ancestry individuals NA NR [NR] (imputed) 9 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90132974 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Coffee type: Ground or instant vs other or decaffeinated (UKB data field 1508) 353,710 European ancestry individuals NA NR [NR] (imputed) 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90132975 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Ground coffee consumption 353,710 European ancestry individuals NA NR [NR] (imputed) 1 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90132976 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cooked vegetables consumption 444,190 European ancestry individuals NA NR [NR] (imputed) 11 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132977 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Raw vegetable consumption 443,633 European ancestry individuals NA NR [NR] (imputed) 11 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132978 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Fresh fruit consumption 447,401 European ancestry individuals NA NR [NR] (imputed) 45 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132979 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Dried fruit consumption 444,741 European ancestry individuals NA NR [NR] (imputed) 11 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132980 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Alcohol drinker status: current or former vs never (UKB data field 20117) 448,623 European ancestry individuals NA NR [NR] (imputed) 1 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST90132923 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Alcohol drinker status: current vs never (UKB data field 20117) 433,353 European ancestry individuals NA NR [NR] (imputed) 1 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST90132924 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Drinks usually with meals in current drinkers (yes and it varies vs no) (UKB data field 1618) 357,136 European ancestry individuals NA NR [NR] (imputed) 2 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST90132925 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Drinks usually with meals in current drinkers (yes vs no) (UKB data field 1618) 235,312 European ancestry individuals NA NR [NR] (imputed) 11 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST90132926 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat eggs vs no eggs, dairy, wheat or sugar restrictions (UKB data field 6144) 357,255 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132927 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat eggs vs no eggs restrictions (UKB data field 6144) 447,391 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132928 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat dairy vs no eggs, dairy, wheat or sugar restrictions (UKB data field 6144) 355,549 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132929 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat dairy vs no dairy restrictions (UKB data field 6144) 447,391 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132930 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat wheat vs no eggs, dairy, wheat or sugar restrictions (UKB data field 6144) 357,603 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132931 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat wheat vs no wheat restrictions (UKB data field 6144) 447,391 European ancestry individuals NA NR [NR] (imputed) 3 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132932 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat sugar vs no eggs, dairy, wheat or sugar restrictions (UKB data field 6144) 427,790 European ancestry individuals NA NR [NR] (imputed) 4 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST90132933 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Never eat sugar vs no sugar restrictions (UKB data field 6144) 447,391 European ancestry individuals NA NR [NR] (imputed) 10 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST90132934 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Dairy-based milk vs never have milk (UKB data field 1418) 427,252 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132935 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Any milk vs never have milk (UKB data field 1418) 448,698 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132936 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Full cream vs never have milk (UKB data field 1418) 43,995 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132937 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Full cream (UKB data field 1418_1) 448,698 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132938 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Semi-skimmed vs never have milk (UKB data field 1418) 308,029 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132939 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Semi-skimmed (UKB data field 1418_2) 448,698 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132940 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 18 449,210 European ancestry individuals NA NR [NR] (imputed) 10 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133023 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 19 449,210 European ancestry individuals NA NR [NR] (imputed) 9 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133024 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 20 449,210 European ancestry individuals NA NR [NR] (imputed) 6 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133025 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 21 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133026 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 22 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133027 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 23 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133028 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 24 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133029 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 25 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133030 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 26 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133031 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 27 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133032 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 28 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133033 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 29 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133034 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 30 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133035 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 31 449,210 European ancestry individuals NA NR [NR] (imputed) 3 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133036 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 32 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133037 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 33 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133038 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 34 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133039 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 35 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133040 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 36 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133041 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 37 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133042 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 38 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133043 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 39 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133044 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 40 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133045 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 41 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133046 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 42 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133047 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Skimmed vs never have milk (UKB data field 1418) 108,035 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132941 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Skimmed (UKB data field 1418_3) 448,698 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132942 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Soy milk vs never have milk (UKB data field 1418) 31,889 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132943 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Soya (UKB data field 1418_4) 448,698 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132944 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Other milk vs never have milk (UKB data field 1418) 20,557 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132945 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type used: Other type of milk (UKB data field 1418_5) 448,698 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132946 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: All spreads vs never use spread (UKB data field 1428) 448,696 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132947 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Butter and margarine vs never use spread (UKB data field 1428) 281,792 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132948 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Any oil based spread vs never use spread (UKB data field 1428) 186,666 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132949 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Butter and butter-like spreads vs oil-based spreads (UKB data field 1428) 371,119 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132950 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Butter and margarine spreads vs oil-based spreads (UKB data field 1428) 333,836 European ancestry individuals NA NR [NR] (imputed) 5 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132951 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Butter vs never use spread (UKB data field 1428) 213,549 European ancestry individuals NA NR [NR] (imputed) 3 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132952 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Butter/spreadable butter (UKB data field 1428_1) 448,696 European ancestry individuals NA NR [NR] (imputed) 5 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132953 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Tub margarine vs never use spread (UKB data field 1428) 77,738 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132954 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Tub margarine (UKB data field 1428) 448,696 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132955 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Flora/Benecol vs never use spread (UKB data field 1428) 86,823 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132956 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Flora Pro-Active/Benecol (UKB data field 1428_2) 448,696 European ancestry individuals NA NR [NR] (imputed) 10 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132957 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Olive oil spread vs never use spread (UKB data field 1428) 106,711 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132958 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Non-butter spread type details: Olive oil based spread (eg: Bertolli) (UKB data field 2654_6) 448,696 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132959 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Other oil-based spread vs never use spread (UKB data field 1428) 128,390 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132960 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Other oil-based spread (UKB data field 1428) 448,696 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132961 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Low fat spread vs never use spread (UKB data field 1428) 72,017 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132962 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Spread type: Low fat spread (UKB data field 1428) 448,696 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132963 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Bread type: White (UKB data field 1448_1) 434,087 European ancestry individuals NA NR [NR] (imputed) 4 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132964 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Bread type: Brown (UKB data field 1448_2) 434,087 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132965 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 43 449,210 European ancestry individuals NA NR [NR] (imputed) 7 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133048 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 44 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133049 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 45 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133050 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 46 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133051 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 47 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133052 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 48 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133053 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 49 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133054 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 50 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133055 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 52 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133056 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 53 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133057 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 54 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133058 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 55 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133059 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 57 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133060 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 58 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133061 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 62 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133062 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 65 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133063 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 67 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133064 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 81 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133065 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Lamb or mutton consumption (UKB data field 1379) 446,443 European ancestry individuals NA NR [NR] (imputed) 9 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132998 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Pork consumption 446,607 European ancestry individuals NA NR [NR] (imputed) 7 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90132999 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Cheese consumption 438,453 European ancestry individuals NA NR [NR] (imputed) 27 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133000 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Added salt consumption 448,890 European ancestry individuals NA NR [NR] (imputed) 45 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133001 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Drink temperature 448,817 European ancestry individuals NA NR [NR] (imputed) 29 beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010088 GCST90133002 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Alcohol consumption 448,623 European ancestry individuals NA NR [NR] (imputed) 29 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90133003 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Alcohol usually taken with meals (UKB data field 1618) 357,136 European ancestry individuals NA NR [NR] (imputed) 5 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST90133004 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Milk type: Skimmed, semi-skimmed or full cream (UKB data field 1418) 427,252 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133005 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 1 449,210 European ancestry individuals NA NR [NR] (imputed) 67 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133006 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 2 449,210 European ancestry individuals NA NR [NR] (imputed) 4 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133007 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 3 449,210 European ancestry individuals NA NR [NR] (imputed) 36 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133008 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 4 449,210 European ancestry individuals NA NR [NR] (imputed) 13 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133009 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 5 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133010 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 6 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133011 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 7 449,210 European ancestry individuals NA NR [NR] (imputed) 17 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133012 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 8 449,210 European ancestry individuals NA NR [NR] (imputed) 11 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133013 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 9 449,210 European ancestry individuals NA NR [NR] (imputed) 5 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133014 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 10 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133015 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 11 449,210 European ancestry individuals NA NR [NR] (imputed) 5 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133016 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 12 449,210 European ancestry individuals NA NR [NR] (imputed) 4 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133017 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 13 449,210 European ancestry individuals NA NR [NR] (imputed) 7 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133018 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 14 449,210 European ancestry individuals NA NR [NR] (imputed) 3 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133019 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 15 449,210 European ancestry individuals NA NR [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133020 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 16 449,210 European ancestry individuals NA NR [NR] (imputed) 2 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133021 Genome-wide genotyping array 2022-08-30 32193382 Cole JB 2020-03-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32193382 Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations. Principal component-derived dietary pattern 17 449,210 European ancestry individuals NA NR [NR] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90133022 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Preeclampsia 88 Hispanic or Latin American trios NA Affymetrix [NR] 1 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90132262 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Preeclampsia (maternal genotype effect) 88 Hispanic or Latin American trios NA Affymetrix [NR] 0 preeclampsia, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90132263 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Preeclampsia (paternal genotype effect) 88 Hispanic or Latin American trios NA Affymetrix [NR] 0 preeclampsia, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0000668, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90132264 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Preeclampsia 254 Hispanic or Latin American mother cases, 70 Hispanic or Latin American mother controls NA Affymetrix [NR] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90132265 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Preeclampsia 225 Hispanic or Latin American fetal cases, 60 Hispanic or Latin American fetal controls NA Affymetrix [NR] 1 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90132266 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Preeclampsia 254 Hispanic or Latin American mother cases, 621 Hispanic or Latin American mother controls NA Affymetrix [NR] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90132267 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Preeclampsia 225 Hispanic or Latin American fetal cases, 611 Hispanic or Latin American fetal controls NA Affymetrix [NR] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90132268 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Gestational age (fetal effect) 251 Hispanic or Latin American mothers NA Affymetrix [NR] 4 gestational age, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0007959 GCST90132269 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Gestational age (maternal effect) 251 Hispanic or Latin American mothers NA Affymetrix [NR] 3 gestational age, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90132270 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Diastolic blood pressure in preeclampsia 252 Hispanic or Latin American mothers NA Affymetrix [NR] 2 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90132271 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Systolic blood pressure in preeclampsia 252 Hispanic or Latin American mothers NA Affymetrix [NR] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90132272 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Severity of diagnosis of preeclampsia 254 Hispanic or Latin American mothers NA Affymetrix [NR] 1 preeclampsia severity measurement http://www.ebi.ac.uk/efo/EFO_0021792 GCST90132273 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Proteinuria in preeclampsia 254 Hispanic or Latin American mothers NA Affymetrix [NR] 2 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90132274 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Gestational age (fetal effect) 223 Hispanic or Latin American offsprings NA Affymetrix [NR] 1 gestational age, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0007959 GCST90132275 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Gestational age (maternal effect) 223 Hispanic or Latin American offsprings NA Affymetrix [NR] 3 gestational age, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90132276 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Diastolic blood pressure in preeclampsia 224 Hispanic or Latin American offsprings NA Affymetrix [NR] 1 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90132277 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Systolic blood pressure in preeclampsia 224 Hispanic or Latin American offsprings NA Affymetrix [NR] 1 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90132278 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Severity of diagnosis of preeclampsia 225 Hispanic or Latin American offsprings NA Affymetrix [NR] 0 preeclampsia severity measurement http://www.ebi.ac.uk/efo/EFO_0021792 GCST90132279 Genome-wide genotyping array 2022-08-22 35588731 Nieves-Colon MA 2022-05-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35588731 Clotting factor genes are associated with preeclampsia in high-altitude pregnant women in the Peruvian Andes. Proteinuria in preeclampsia 225 Hispanic or Latin American offsprings NA Affymetrix [NR] 3 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90132280 Genome-wide genotyping array 2022-08-25 35698589 An YC 2022-06-07 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35698589 Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. Insomnia in migraine 899 Han Chinese ancestry migraineurs with insomnia, 164 Han Chinese ancestry migraineurs without insomnia NA Affymetrix [686463] 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90132916 Genome-wide genotyping array 2022-08-25 35698589 An YC 2022-06-07 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35698589 Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. Insomnia in migraine 198 Han Chinese ancestry male migraineurs with insomnia, 49 Han Chinese ancestry male migraineurs without insomnia NA Affymetrix [686463] 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90132917 Genome-wide genotyping array 2022-08-25 35698589 An YC 2022-06-07 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35698589 Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. Insomnia in migraine 704 Han Chinese ancestry female migraineurs with insomnia, 112 Han Chinese ancestry female migraineurs without insomnia NA Affymetrix [686463] 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90132918 Genome-wide genotyping array 2022-08-25 35698589 An YC 2022-06-07 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35698589 Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. Insomnia in episodic migraine 731 Han Chinese ancestry migraineurs with insomnia, 143 Han Chinese ancestry migraineurs without insomnia NA Affymetrix [686463] 2 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90132919 Genome-wide genotyping array 2022-08-25 35698589 An YC 2022-06-07 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35698589 Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. Insomnia in chronic migraine 168 Han Chinese ancestry migraineurs with insomnia, 21 Han Chinese ancestry migraineurs without insomnia NA Affymetrix [686463] 12 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90132920 Genome-wide genotyping array 2022-08-25 35698589 An YC 2022-06-07 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35698589 Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. Insomnia in migraine with aura 263 Han Chinese ancestry migraineurs with insomnia, 35 Han Chinese ancestry migraineurs without insomnia NA Affymetrix [686463] 12 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90132921 Genome-wide genotyping array 2022-08-25 35698589 An YC 2022-06-07 Nat Sci Sleep www.ncbi.nlm.nih.gov/pubmed/35698589 Identification of Novel Genetic Variants Associated with Insomnia and Migraine Comorbidity. Insomnia in migraine without aura 636 Han Chinese ancestry migraineurs with insomnia, 129 Han Chinese ancestry migraineurs without insomnia NA Affymetrix [686463] 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90132922 Genome-wide genotyping array 2022-08-22 34396400 Zheng X 2021-08-01 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/34396400 Host Genetic Risk Factors for Chlamydia trachomatis-Related Infertility in Women. Chlamydia trachomatis-related tubal factor infertility 74 European ancestry cases, 208 European ancestry controls, 33 Black cases, 52 Black controls, 6 Hispanic or Latino cases, 8 Hispanic or Latino controls, 4 Asian ancestry cases, 8 Asian ancestry controls, 2 cases, 1 controls NA Illumina [NR] (imputed) 6 tubal factor infertility, Chlamydophila infectious disease http://www.ebi.ac.uk/efo/EFO_0021795, http://www.ebi.ac.uk/efo/EFO_1000863 GCST90044915 Genome-wide genotyping array 2022-08-16 35274129 Verdiesen RMG 2022-03-11 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/35274129 Genome-wide association study meta-analysis identifies three novel loci for circulating anti-Müllerian hormone levels in women. Anti-Mullerian hormone levels 7,049 European ancestry individuals NA Illumina [8298138] (imputed) 4 anti-Mullerian hormone measurement http://www.ebi.ac.uk/efo/EFO_0004769 GCST90104596 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Multisyllabic word repetition 432 European ancestry children from 148 families NA Illumina [NR] (imputed) 5 oral motor function measurement http://www.ebi.ac.uk/efo/EFO_0021793 GCST90027030 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Nonsense word repetition 431 European ancestry children from 148 families NA Illumina [NR] (imputed) 1 oral motor function measurement http://www.ebi.ac.uk/efo/EFO_0021793 GCST90027031 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Diadochokinetic rates 419 European ancestry children from 148 families NA Illumina [NR] (imputed) 2 oral motor function measurement http://www.ebi.ac.uk/efo/EFO_0021793 GCST90027032 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Comprehensive listening 165 European ancestry children from 148 families NA Illumina [NR] (imputed) 2 receptive language perception http://www.ebi.ac.uk/efo/EFO_0005686 GCST90027033 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Word attack subtest 165 European ancestry children from 148 families NA Illumina [NR] (imputed) 1 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST90027034 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Expressive language ability 325 European ancestry children from 148 families NA Illumina [NR] (imputed) 2 infant expressive language ability http://www.ebi.ac.uk/efo/EFO_0006316 GCST90027035 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Written spelling 298 European ancestry children from 148 families NA Illumina [NR] (imputed) 5 reading and spelling ability http://www.ebi.ac.uk/efo/EFO_0005301 GCST90027036 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Percent phonemes correct for nonsense word repetition 431 European ancestry children from 148 families NA Illumina [NR] (imputed) 3 oral motor function measurement http://www.ebi.ac.uk/efo/EFO_0021793 GCST90027037 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Phonological awareness (Elision) 299 European ancestry children from 148 families NA Illumina [NR] (imputed) 4 receptive language perception http://www.ebi.ac.uk/efo/EFO_0005686 GCST90027038 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Nonsense word reading 398 European ancestry children from 148 families NA Illumina [NR] (imputed) 1 non-word reading http://www.ebi.ac.uk/efo/EFO_0005299 GCST90027039 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Receptive language ability 325 European ancestry children from 148 families NA Illumina [NR] (imputed) 2 receptive language perception http://www.ebi.ac.uk/efo/EFO_0005686 GCST90027040 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Percent phonemes correct for multisyllabic word repetition 432 European ancestry children from 148 families NA Illumina [NR] (imputed) 0 oral motor function measurement http://www.ebi.ac.uk/efo/EFO_0021793 GCST90132308 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Peabody picture vocabulary 399 European ancestry children from 148 families NA Illumina [NR] (imputed) 0 infant expressive language ability http://www.ebi.ac.uk/efo/EFO_0006316 GCST90132309 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Expressive one word vocabulary 364 European ancestry children from 148 families NA Illumina [NR] (imputed) 0 infant expressive language ability http://www.ebi.ac.uk/efo/EFO_0006316 GCST90132310 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Woodcock nonsense word reading 399 European ancestry children from 148 families NA Illumina [NR] (imputed) 0 word reading http://www.ebi.ac.uk/efo/EFO_0005300 GCST90132311 Genome-wide genotyping array 2022-08-19 34315907 Benchek P 2021-07-27 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34315907 Association between genes regulating neural pathways for quantitative traits of speech and language disorders. Rapid automatised naming (colors) 309 European ancestry children from 148 families NA Illumina [NR] (imputed) 0 infant expressive language ability http://www.ebi.ac.uk/efo/EFO_0006316 GCST90132312 Genome-wide genotyping array 2022-09-01 35748965 Saul N 2022-06-24 Biogerontology www.ncbi.nlm.nih.gov/pubmed/35748965 Identification of healthspan-promoting genes in Caenorhabditis elegans based on a human GWAS study. Increased healthspan in old age 750 Finnish ancestry healthy elderly cases, 1,502 Finnish ancestry unhealthy elderly controls NA Affymetrix, Illumina [9600000] (imputed) 5 healthspan http://www.ebi.ac.uk/efo/EFO_0009762 GCST90134247 Genome-wide genotyping array 2022-09-01 35748965 Saul N 2022-06-24 Biogerontology www.ncbi.nlm.nih.gov/pubmed/35748965 Identification of healthspan-promoting genes in Caenorhabditis elegans based on a human GWAS study. Increased healthspan 750 Finnish ancestry healthy elderly cases, 1,502 Finnish ancestry unhealthy elderly controls, 2,663 Finnish ancestry all-cause mortality controls NA Affymetrix, Illumina [9600000] (imputed) 6 healthspan http://www.ebi.ac.uk/efo/EFO_0009762 GCST90134248 Genome-wide genotyping array 2022-08-31 35752286 Ho MF 2022-06-22 Mol Metab www.ncbi.nlm.nih.gov/pubmed/35752286 Genome-wide association study for circulating FGF21 in patients with alcohol use disorder: Molecular links between the SNHG16 locus and catecholamine metabolism. FGF21 levels in alcohol use disorder 442 individuals NA NR [NR] (imputed) 1 fibroblast growth factor 21 measurement http://www.ebi.ac.uk/efo/EFO_0010783 GCST90133378 Genome-wide genotyping array 2022-08-31 35783123 Yeh PK 2022-06-15 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35783123 Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine. Subjective cognitive decline in migraine 700 East Asian ancestry cases, 319 East Asian ancestry controls NA Affymetrix [NR] 1 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST90133376 Genome-wide genotyping array 2022-08-31 35783123 Yeh PK 2022-06-15 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35783123 Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine. Subjective cognitive decline in episodic migraine 565 East Asian ancestry cases, 270 East Asian ancestry controls NA Affymetrix [NR] 1 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST90133372 Genome-wide genotyping array 2022-08-31 35783123 Yeh PK 2022-06-15 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35783123 Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine. Subjective cognitive decline in chronic migraine 135 East Asian ancestry cases, 49 East Asian ancestry controls NA Affymetrix [NR] 2 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST90133373 Genome-wide genotyping array 2022-08-31 35783123 Yeh PK 2022-06-15 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35783123 Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine. Subjective cognitive decline in migraine without aura 496 East Asian ancestry cases, 232 East Asian ancestry controls NA Affymetrix [NR] 2 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST90133374 Genome-wide genotyping array 2022-08-31 35783123 Yeh PK 2022-06-15 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35783123 Genetic Variants Associated With Subjective Cognitive Decline in Patients With Migraine. Subjective cognitive decline 205 East Asian ancestry cases, 186 East Asian ancestry controls NA Affymetrix [NR] 2 cognitive decline measurement http://www.ebi.ac.uk/efo/EFO_0007710 GCST90133375 Genome-wide genotyping array 2022-08-19 35912057 Ko YL 2021-11-24 Tzu Chi Med J www.ncbi.nlm.nih.gov/pubmed/35912057 Genetics of hyperuricemia and gout: Insights from recent genome-wide association studies and Mendelian randomization studies. Serum uric acid levels 23,067 East Asian ancestry individuals NA NR [NR] 0 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90132285 Genome-wide genotyping array 2022-08-25 35658861 You D 2022-06-06 BMC Med www.ncbi.nlm.nih.gov/pubmed/35658861 Associations of genetic risk, BMI trajectories, and the risk of non-small cell lung cancer: a population-based cohort study. Non-small cell lung cancer x BMI trajectory interaction 1,074 European ancestry cases, 11,128 European ancestry controls, 72 Black cases, 993 Black controls, 26 Hispanic controls, 62 Asian ancestry controls, 10 controls NA Illumina [4250895] (imputed) 4 longitudinal BMI measurement, non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0005937, http://www.ebi.ac.uk/efo/EFO_0003060 GCST90132908 Genome-wide genotyping array 2022-09-29 34131076 Wu Y 2021-06-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/34131076 Estimating genetic nurture with summary statistics of multigenerational genome-wide association studies. Educational attainment (direct effects) 24,434 European ancestry individuals NA NR [9030402] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90017139 Genome-wide genotyping array 2022-09-29 34131076 Wu Y 2021-06-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/34131076 Estimating genetic nurture with summary statistics of multigenerational genome-wide association studies. Educational attainment (indirect effects) 37,081 European ancestry individuals NA NR [9030402] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90017140 Genome-wide genotyping array 2022-09-29 34131076 Wu Y 2021-06-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/34131076 Estimating genetic nurture with summary statistics of multigenerational genome-wide association studies. Birth weight (direct effects) 140,896 European ancestry individuals NA NR [11936014] (imputed) 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90017141 Genome-wide genotyping array 2022-09-29 34131076 Wu Y 2021-06-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/34131076 Estimating genetic nurture with summary statistics of multigenerational genome-wide association studies. Birth weight (indirect effects) 446,108 European ancestry individuals NA NR [11936014] (imputed) 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90017142 Genome-wide genotyping array 2022-08-18 35545683 Sorosina M 2022-05-12 J Neurol www.ncbi.nlm.nih.gov/pubmed/35545683 A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility. Multiple sclerosis 1,701 Italian ancestry cases, 2,345 Italian ancestry controls 4,991 European ancestry cases, 8,028 European ancestry controls Illumina [196524] (imputed) 5 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90132190 Genome-wide genotyping array 2022-09-27 35396580 Trubetskoy V 2022-04-08 Nature www.ncbi.nlm.nih.gov/pubmed/35396580 Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Schizophrenia 53,386 European ancestry cases, 77,258 European ancestry controls, 14,004 East Asian ancestry cases, 16,757 East Asian ancestry controls, 6,152 African American cases, 3,918 African American controls, 1,234 Latino cases, 3,090 Latino controls 1,979 European ancestry cases, 142,626 European ancestry controls Affymetrix [7585078] (imputed) 1117 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90128471 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in bladder cancer 526 White ancestry individuals NA Affymetrix [8326282] (imputed) 0 urinary bladder carcinoma, overall survival http://purl.obolibrary.org/obo/MONDO_0004986, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90140995 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Multiple myeloma specific survival 355 White ancestry individuals NA Affymetrix [8258091] (imputed) 0 survival time, multiple myeloma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0001378 GCST90141021 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Oral and pharynx cancer specific survival 458 White ancestry individuals NA Affymetrix [8272464] (imputed) 0 oropharynx cancer, survival time http://www.ebi.ac.uk/efo/EFO_1001931, http://www.ebi.ac.uk/efo/EFO_0000714 GCST90141022 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Ovarian cancer specific survival 437 White ancestry individuals NA Affymetrix [8351777] (imputed) 0 survival time, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0001075 GCST90141023 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Pancreatic cancer specific survival 506 White ancestry individuals NA Affymetrix [8299001] (imputed) 0 survival time, pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0002618 GCST90141024 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in multiple myeloma 355 White ancestry individuals NA Affymetrix [8258091] (imputed) 0 overall survival, multiple myeloma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0001378 GCST90141004 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Renal cancer specific survival 649 White ancestry individuals NA Affymetrix [8376852] (imputed) 0 renal carcinoma, survival time http://www.ebi.ac.uk/efo/EFO_0002890, http://www.ebi.ac.uk/efo/EFO_0000714 GCST90141026 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Skin melanoma specific survival 1,402 White ancestry individuals NA Affymetrix [8339443] (imputed) 0 survival time, melanoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000756 GCST90141027 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Thyroid cancer specific survival 179 White ancestry individuals NA Affymetrix [8308306] (imputed) 0 survival time, thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0002892 GCST90141028 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in renal cancer 649 White ancestry individuals NA Affymetrix [8376852] (imputed) 0 renal carcinoma, overall survival http://www.ebi.ac.uk/efo/EFO_0002890, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90141009 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in skin melanoma 1,402 White ancestry individuals NA Affymetrix [8339443] (imputed) 0 overall survival, melanoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0000756 GCST90141010 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in thyroid cancer 179 White ancestry individuals NA Affymetrix [8308306] (imputed) 0 overall survival, thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0002892 GCST90141011 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Bladder cancer specific survival 526 White ancestry individuals NA Affymetrix [8326282] (imputed) 0 survival time, urinary bladder carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/MONDO_0004986 GCST90141012 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Brain cancer specific survival 397 White ancestry individuals NA Affymetrix [8390743] (imputed) 0 brain neoplasm, survival time http://www.ebi.ac.uk/efo/EFO_0003833, http://www.ebi.ac.uk/efo/EFO_0000714 GCST90141013 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Breast cancer specific survival 4,350 White ancestry individuals NA Affymetrix [8338638] (imputed) 0 survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90141014 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Colorectal cancer specific survival 2,621 White ancestry individuals NA Affymetrix [8334629] (imputed) 0 survival time, colorectal carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1001951 GCST90141015 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Corpus uteri specific survival 698 White ancestry individuals NA Affymetrix [8360934] (imputed) 0 survival time, uterine corpus cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0007532 GCST90141016 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Esophagus cancer specific survival 460 White ancestry individuals NA Affymetrix [8296714] (imputed) 0 survival time, esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0002916 GCST90141017 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Gastric cancer specific survival 303 White ancestry individuals NA Affymetrix [8283963] (imputed) 0 survival time, gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000178 GCST90141018 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Lung cancer specific survival 1,700 White ancestry individuals NA Affymetrix [8355227] (imputed) 0 lung carcinoma, survival time http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0000714 GCST90141019 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Lymphoid leukaemia specific survival 350 White ancestry individuals NA Affymetrix [8425952] (imputed) 0 survival time, lymphoid leukemia http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0004289 GCST90141020 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in brain cancer 397 White ancestry individuals NA Affymetrix [8390743] (imputed) 0 brain neoplasm, overall survival http://www.ebi.ac.uk/efo/EFO_0003833, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90140996 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in breast cancer 4,350 White ancestry individuals NA Affymetrix [8338638] (imputed) 0 overall survival, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90140997 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in colorectal cancer 2,621 White ancestry individuals NA Affymetrix [8334629] (imputed) 0 overall survival, colorectal carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1001951 GCST90140998 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in corpus uteri 698 White ancestry individuals NA Affymetrix [8360934] (imputed) 0 uterine corpus cancer, overall survival http://www.ebi.ac.uk/efo/EFO_0007532, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90140999 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in esophagus cancer 460 White ancestry individuals NA Affymetrix [8296714] (imputed) 0 esophageal carcinoma, overall survival http://www.ebi.ac.uk/efo/EFO_0002916, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90141000 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in gastric cancer 303 White ancestry individuals NA Affymetrix [8283963] (imputed) 0 overall survival, gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0000178 GCST90141001 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in lung cancer 1,700 White ancestry individuals NA Affymetrix [8355227] (imputed) 0 lung carcinoma, overall survival http://www.ebi.ac.uk/efo/EFO_0001071, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90141002 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in lymphoid leukaemia 350 White ancestry individuals NA Affymetrix [8425952] (imputed) 0 overall survival, lymphoid leukemia http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0004289 GCST90141003 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Prostate cancer specific survival 4,882 White ancestry individuals NA Affymetrix [8333069] (imputed) 0 survival time, prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0001663 GCST90141025 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in oral and pharynx cancer 458 White ancestry individuals NA Affymetrix [8272464] (imputed) 0 oropharynx cancer, overall survival http://www.ebi.ac.uk/efo/EFO_1001931, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90141005 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in ovarian cancer 437 White ancestry individuals NA Affymetrix [8351777] (imputed) 0 overall survival, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0001075 GCST90141006 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in pancreatic cancer 506 White ancestry individuals NA Affymetrix [8299001] (imputed) 0 overall survival, pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0002618 GCST90141007 Genome-wide genotyping array 2022-09-29 35947748 Xin J 2022-08-10 Nucleic Acids Res www.ncbi.nlm.nih.gov/pubmed/35947748 SUMMER: a Mendelian randomization interactive server to systematically evaluate the causal effects of risk factors and circulating biomarkers on pan-cancer survival. Overall survival in prostate cancer 4,882 White ancestry individuals NA Affymetrix [8333069] (imputed) 0 prostate carcinoma, overall survival http://www.ebi.ac.uk/efo/EFO_0001663, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90141008 Genome-wide genotyping array 2022-10-12 34573423 Buono RJ 2021-09-18 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34573423 Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. Generalized epilepsy 684 European ancestry cases, 9,861 European ancestry controls NA Illumina [NR] (imputed) 5 generalised epilepsy http://www.ebi.ac.uk/efo/EFO_0005917 GCST90053845 Genome-wide genotyping array 2022-10-12 34573423 Buono RJ 2021-09-18 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34573423 Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. Generalized epilepsy 143 African American cases, 4,627 African American controls NA Illumina [NR] (imputed) 2 generalised epilepsy http://www.ebi.ac.uk/efo/EFO_0005917 GCST90053846 Genome-wide genotyping array 2022-10-12 34573423 Buono RJ 2021-09-18 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34573423 Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. Generalized epilepsy 684 European ancestry cases, 9,861 European ancestry controls, 143 African American cases, 4,627 African American controls NA Illumina [NR] (imputed) 2 generalised epilepsy http://www.ebi.ac.uk/efo/EFO_0005917 GCST90053847 Genome-wide genotyping array 2022-10-12 34573423 Buono RJ 2021-09-18 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34573423 Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. Focal epilepsy 756 European ancestry cases, 9,861 European ancestry controls NA Illumina [NR] (imputed) 1 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90053848 Genome-wide genotyping array 2022-10-12 34573423 Buono RJ 2021-09-18 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34573423 Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. Focal epilepsy 208 African American cases, 4,627 African American controls NA Illumina [NR] (imputed) 6 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90053849 Genome-wide genotyping array 2022-10-12 34573423 Buono RJ 2021-09-18 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34573423 Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized Epilepsy. Focal epilepsy 756 European ancestry cases, 9,861 European ancestry controls, 208 African American cases, 4,627 African American controls NA Illumina [NR] (imputed) 3 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90053850 Genome-wide genotyping array 2022-10-12 34959947 Eszlari N 2021-12-08 Nutrients www.ncbi.nlm.nih.gov/pubmed/34959947 Biology of Perseverative Negative Thinking: The Role of Timing and Folate Intake. Rumination in optimal folate intake 30,213 British ancestry cases, 31,770 British ancestry controls NA NR [6012113] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90101802 Genome-wide genotyping array 2022-10-12 34959947 Eszlari N 2021-12-08 Nutrients www.ncbi.nlm.nih.gov/pubmed/34959947 Biology of Perseverative Negative Thinking: The Role of Timing and Folate Intake. Rumination in suboptimal folate intake 5,180 British ancestry cases, 5,458 British ancestry controls NA NR [5992065] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90101800 Genome-wide genotyping array 2022-10-12 34959947 Eszlari N 2021-12-08 Nutrients www.ncbi.nlm.nih.gov/pubmed/34959947 Biology of Perseverative Negative Thinking: The Role of Timing and Folate Intake. Rumination 35,393 British ancestry cases, 37,228 British ancestry controls NA NR [6013935] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90101798 Genome-wide genotyping array 2022-10-12 34959947 Eszlari N 2021-12-08 Nutrients www.ncbi.nlm.nih.gov/pubmed/34959947 Biology of Perseverative Negative Thinking: The Role of Timing and Folate Intake. Worry in optimal folate intake 33,863 British ancestry cases, 28,120 British ancestry controls NA NR [6012113] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90101803 Genome-wide genotyping array 2022-10-12 34959947 Eszlari N 2021-12-08 Nutrients www.ncbi.nlm.nih.gov/pubmed/34959947 Biology of Perseverative Negative Thinking: The Role of Timing and Folate Intake. Worry in suboptimal folate intake 5,927 British ancestry cases, 4,711 British ancestry controls NA NR [5992065] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90101801 Genome-wide genotyping array 2022-10-12 34959947 Eszlari N 2021-12-08 Nutrients www.ncbi.nlm.nih.gov/pubmed/34959947 Biology of Perseverative Negative Thinking: The Role of Timing and Folate Intake. Worry 39,790 British ancestry cases, 32,831 British ancestry controls NA NR [6013935] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90101799 Genome-wide genotyping array 2022-09-23 36009466 Hsu CC 2022-08-08 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36009466 Polygenic Risk Score Improves Cataract Prediction in East Asian Population. Age-related cataracts 5,120 Han Chinese ancestry cases (>=60 years old), 13,256 Han Chinese ancestry controls 2,246 Han Chinese ancestry cases (>=60 years old), 4,990 Han Chinese ancestry controls NR [11110260] (imputed) 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90137958 Genome-wide genotyping array 2022-09-23 36009466 Hsu CC 2022-08-08 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36009466 Polygenic Risk Score Improves Cataract Prediction in East Asian Population. Cataract 1,959 Han Chinese ancestry cases (<60 years old), 13,256 Han Chinese ancestry controls 757 Han Chinese ancestry cases (<60 years old), 4,990 Han Chinese ancestry controls NR [11110260] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90137959 Genome-wide genotyping array 2022-09-23 36009466 Hsu CC 2022-08-08 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36009466 Polygenic Risk Score Improves Cataract Prediction in East Asian Population. Cataract 7,079 Han Chinese ancestry cases, 13,256 Han Chinese ancestry controls NA NR [11110260] (imputed) 13 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90137960 Genome-wide genotyping array 2022-08-24 35977952 Dixon PH 2022-08-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35977952 GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements. Intrahepatic cholestasis of pregnancy 1,138 European ancestry cases, 153,642 European ancestry controls NA Affymetrix, Illumina [7715762] (imputed) 11 Intrahepatic cholestasis of pregnancy http://www.ebi.ac.uk/efo/EFO_0009048 GCST90095084 Genome-wide genotyping array, Genome-wide sequencing 2022-10-27 34689653 Awotoye W 2021-10-23 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34689653 Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. Nonsyndromic orofacial cleft x sex interaction 1,019 Sub-Saharan African ancestry cases, 2,159 Sub-Saharan African ancestry controls NA Illumina [603101] (imputed) 74 orofacial cleft, sex interaction measurement http://purl.obolibrary.org/obo/MONDO_0000358, http://www.ebi.ac.uk/efo/EFO_0008343 GCST90093361 Genome-wide genotyping array 2022-10-27 34689653 Awotoye W 2021-10-23 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34689653 Genome-wide Gene-by-Sex Interaction Studies Identify Novel Nonsyndromic Orofacial Clefts Risk Locus. Nonsyndromic orofacial cleft x sex interaction (2df) 1,019 Sub-Saharan African ancestry cases, 2,159 Sub-Saharan African ancestry controls NA Illumina [603101] (imputed) 83 orofacial cleft, sex interaction measurement http://purl.obolibrary.org/obo/MONDO_0000358, http://www.ebi.ac.uk/efo/EFO_0008343 GCST90093362 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Leisure screen time 526,725 European ancestry individuals NA Affymetrix, Illumina [20320957] (imputed) 89 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104339 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Leisure screen time 545,263 European ancestry, East Asian ancestry, South Asian ancestry, Hispanic or Latin American, African ancestry individuals NA Affymetrix, Illumina [8493099] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104340 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Moderate-to-vigorous intensity physical activity during leisure time 608,595 European ancestry individuals NA Affymetrix, Illumina [22586718] (imputed) 8 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104341 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Moderate-to-vigorous intensity physical activity during leisure time 636,924 European ancestry, East Asian ancestry, South Asian ancestry, Hispanic or Latin American, African ancestry individuals NA Affymetrix, Illumina [49915722] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104342 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Sedentary commuting 159,606 European ancestry individuals NA Affymetrix, Illumina [19128325] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104343 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Sedentary commuting 163,977 European ancestry, East Asian ancestry, South Asian ancestry, Hispanic or Latin American, African ancestry individuals NA Affymetrix, Illumina [40677400] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104344 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Sedentary behavior at work 372,609 European ancestry individuals NA Affymetrix, Illumina [21968520] (imputed) 5 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104345 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Sedentary behavior at work 391,051 European ancestry, East Asian ancestry, South Asian ancestry, Hispanic or Latin American, African ancestry individuals NA Affymetrix, Illumina [47070757] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90104346 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Moderate-to-vigorous intensity physical activity during leisure time up to 608,595 European ancestry men NA Affymetrix, Illumina [NR] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90137456 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Moderate-to-vigorous intensity physical activity during leisure time up to 608,595 European ancestry women NA Affymetrix, Illumina [NR] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90137457 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Leisure screen time (MTAG) 526,725 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 8 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90137458 Genome-wide genotyping array 2022-09-21 36071172 Wang Z 2022-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36071172 Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention. Moderate-to-vigorous intensity physical activity during leisure time (MTAG) 608,595 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 8 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90137459 Genome-wide genotyping array 2022-10-03 36035146 Wang P 2022-08-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/36035146 Novel genetic associations with five aesthetic facial traits: A genome-wide association study in the Chinese population. Widow's peak 4,903 Chinese ancestry cases, 4,612 Chinese ancestry controls 1,259 Chinese ancestry cases, 1,172 Chinese ancestry controls Affymetrix [NR] 1 Widow's peak http://purl.obolibrary.org/obo/HP_0000349 GCST90146356 Genome-wide genotyping array 2022-10-03 36035146 Wang P 2022-08-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/36035146 Novel genetic associations with five aesthetic facial traits: A genome-wide association study in the Chinese population. Unibrow 2,364 Chinese ancestry cases, 3,416 Chinese ancestry controls 603 Chinese ancestry cases, 871 Chinese ancestry controls Affymetrix [NR] 0 synophrys measurement http://www.ebi.ac.uk/efo/EFO_0007906 GCST90146357 Genome-wide genotyping array 2022-10-03 36035146 Wang P 2022-08-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/36035146 Novel genetic associations with five aesthetic facial traits: A genome-wide association study in the Chinese population. Double eyelid 2,182 Chinese ancestry cases, 3,773 Chinese ancestry controls 560 Chinese ancestry cases, 958 Chinese ancestry controls Affymetrix [NR] 0 Accessory eyelid http://purl.obolibrary.org/obo/HP_0430008 GCST90146358 Genome-wide genotyping array 2022-10-03 36035146 Wang P 2022-08-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/36035146 Novel genetic associations with five aesthetic facial traits: A genome-wide association study in the Chinese population. Earlobe attachment 3,477 Chinese ancestry cases, 4,479 Chinese ancestry controls 890 Chinese ancestry cases, 1,131 Chinese ancestry controls Affymetrix [NR] 3 Attached earlobe http://purl.obolibrary.org/obo/HP_0009907 GCST90146359 Genome-wide genotyping array 2022-10-03 36035146 Wang P 2022-08-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/36035146 Novel genetic associations with five aesthetic facial traits: A genome-wide association study in the Chinese population. Freckles 1,548 Chinese ancestry cases, 5,031 Chinese ancestry controls 392 Chinese ancestry cases, 1,280 Chinese ancestry controls Affymetrix [NR] 1 freckles http://www.ebi.ac.uk/efo/EFO_0003963 GCST90146360 Genome-wide genotyping array 2022-10-17 35999217 Akbari P 2022-08-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35999217 Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. BMI-adjusted waist-hip ratio 458,317 European ancestry individuals, 138,792 Hispanic or Latin American individuals, 8,948 African ancestry individuals, 2,203 East Asian ancestry individuals, 10,115 South Asian ancestry individuals NA Illumina [1000000] 13 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90176019 Exome-wide sequencing 2022-10-17 35999217 Akbari P 2022-08-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35999217 Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. BMI-adjusted waist-hip ratio 458,317 European ancestry individuals NA Illumina [1000000] 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90176020 Exome-wide sequencing 2022-10-17 35999217 Akbari P 2022-08-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35999217 Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. BMI-adjusted waist-hip ratio 138,792 Hispanic or Latin American individuals NA Illumina [1000000] 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90176021 Exome-wide sequencing 2022-10-07 35094092 Deakin CT 2022-01-31 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35094092 Association with HLA-DRβ1 position 37 distinguishes juvenile Dermatomyositis from adult-onset myositis. Juvenile dermatomyositis 851 European ancestry cases, 12,232 European ancestry controls NA Illumina [174613] 4 juvenile dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000557 GCST90162630 Genome-wide genotyping array 2022-10-07 35094092 Deakin CT 2022-01-31 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35094092 Association with HLA-DRβ1 position 37 distinguishes juvenile Dermatomyositis from adult-onset myositis. Juvenile dermatomyositis 851 European ancestry cases, 12,232 European ancestry controls NA Illumina [Infinium CoreExome-24 BeadChip] (imputed) 12 juvenile dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000557 GCST90162637 Genome-wide genotyping array 2022-09-26 36043126 Patel B 2022-08-01 Lancet Rheumatol www.ncbi.nlm.nih.gov/pubmed/36043126 Shared genetic susceptibility between trigger finger and carpal tunnel syndrome: a genome-wide association study. Trigger finger 2,908 European ancestry cases, 436,579 European ancestry controls 1,485 European ancestry cases, 137,185 European ancestry controls Affymetrix [21132702] (imputed) 5 stenosing tenosynovitis http://www.ebi.ac.uk/efo/EFO_0010822 GCST90104907 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular end systolic volume 29,498 European ancestry individuals 12,321 European ancestry individuals Affymetrix [9245632] (imputed) 13 right ventricular systolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021815 GCST90134589 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular stroke volume 29,503 European ancestry individuals 12,324 European ancestry individuals Affymetrix [9245594] (imputed) 1 right ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0021817 GCST90134590 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular ejection fraction 29,488 European ancestry individuals 12,307 European ancestry individuals Affymetrix [9245705] (imputed) 10 right ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0021816 GCST90134591 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular end diastolic volume 29,506 European ancestry individuals 12,324 European ancestry individuals Affymetrix [9245599] (imputed) 7 right ventricular diastolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021814 GCST90134588 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular end diastolic volume (MTAG) 29,506 European ancestry individuals 12,324 European ancestry individuals Affymetrix [7158209] (imputed) 4 right ventricular diastolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021814 GCST90134592 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular end systolic volume (MTAG) 29,498 European ancestry individuals 12,321 European ancestry individuals Affymetrix [7158086] (imputed) 0 right ventricular systolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021815 GCST90134593 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular stroke volume (MTAG) 29,503 European ancestry individuals 12,324 European ancestry individuals Affymetrix [7158209] (imputed) 4 right ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0021817 GCST90134594 Genome-wide genotyping array 2022-09-14 35697868 Aung N 2022-06-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35697868 Genome-wide association analysis reveals insights into the genetic architecture of right ventricular structure and function. Right ventricular ejection fraction (MTAG) 29,488 European ancestry individuals 12,307 European ancestry individuals Affymetrix [7158086] (imputed) 4 right ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0021816 GCST90134595 Genome-wide genotyping array 2022-08-24 35762941 Plotnikov D 2022-06-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35762941 High Blood Pressure and Intraocular Pressure: A Mendelian Randomization Study. Systolic blood pressure 526,001 European ancestry individuals NA NR [NR] (imputed) 498 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90132903 Genome-wide genotyping array 2022-08-24 35762941 Plotnikov D 2022-06-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35762941 High Blood Pressure and Intraocular Pressure: A Mendelian Randomization Study. Diastolic blood pressure 526,001 European ancestry individuals NA NR [NR] (imputed) 564 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90132904 Genome-wide genotyping array 2022-08-24 35762941 Plotnikov D 2022-06-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35762941 High Blood Pressure and Intraocular Pressure: A Mendelian Randomization Study. Pulse pressure 526,001 European ancestry individuals NA NR [NR] (imputed) 289 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90132905 Genome-wide genotyping array 2022-10-13 35490390 Ramos J 2022-05-01 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/35490390 Genetic variants in the SHISA6 gene are associated with delayed cognitive impairment in two family datasets. Age at onset of cognitive impairment 1,522 Amish individuals 3,350 European ancestry individuals Illumina [7815951] (imputed) 0 age of onset of cognitive disorder http://purl.obolibrary.org/obo/OBA_2040165 GCST90132307 Genome-wide genotyping array 2022-08-31 35692035 Borges MC 2022-06-13 BMC Med www.ncbi.nlm.nih.gov/pubmed/35692035 Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants. Circulating docosahexaenoic acid levels 114,999 European ancestry individuals NA NR [12321876] (imputed) 46 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90133361 Genome-wide genotyping array 2022-08-31 35692035 Borges MC 2022-06-13 BMC Med www.ncbi.nlm.nih.gov/pubmed/35692035 Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants. Total omega-3 fatty acid levels 114,999 European ancestry individuals NA NR [12321876] (imputed) 49 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90133362 Genome-wide genotyping array 2022-08-31 35692035 Borges MC 2022-06-13 BMC Med www.ncbi.nlm.nih.gov/pubmed/35692035 Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants. Linoleic acid levels 114,999 European ancestry individuals NA NR [12321876] (imputed) 55 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90133363 Genome-wide genotyping array 2022-08-31 35692035 Borges MC 2022-06-13 BMC Med www.ncbi.nlm.nih.gov/pubmed/35692035 Role of circulating polyunsaturated fatty acids on cardiovascular diseases risk: analysis using Mendelian randomization and fatty acid genetic association data from over 114,000 UK Biobank participants. Total omega-6 fatty acid levels 114,999 European ancestry individuals NA NR [12321876] (imputed) 64 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90133364 Genome-wide genotyping array 2022-10-14 34563731 Das SK 2021-09-23 Mol Metab www.ncbi.nlm.nih.gov/pubmed/34563731 Metabolomic Architecture of Obesity Implicates Metabolonic Lactone Sulfate in Cardiometabolic Disease. Metabolonic lactone sulfate levels 1,027 Mexican American individuals 554 African American individuals Illumina [NR] (imputed) 230 X-12063 measurement http://www.ebi.ac.uk/efo/EFO_0021283 GCST90054779 Genome-wide genotyping array 2022-10-14 34563731 Das SK 2021-09-23 Mol Metab www.ncbi.nlm.nih.gov/pubmed/34563731 Metabolomic Architecture of Obesity Implicates Metabolonic Lactone Sulfate in Cardiometabolic Disease. Metabolonic lactone sulfate levels 554 African American individuals NA Illumina [NR] (imputed) 2 X-12063 measurement http://www.ebi.ac.uk/efo/EFO_0021283 GCST90165316 Genome-wide genotyping array 2022-10-12 36203093 Hakkaart C 2022-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36203093 Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers. Breast cancer in BRCA1 pathogenic variant carriers (CNV deletions) 7,725 European ancestry cases, 7,617 European ancestry controls NA Illumina [16395] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90134567 Genome-wide genotyping array 2022-10-12 36203093 Hakkaart C 2022-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36203093 Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers. Breast cancer in BRCA1 pathogenic variant carriers (CNV duplications) 7,725 European ancestry cases, 7,617 European ancestry controls NA Illumina [16395] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90134568 Genome-wide genotyping array 2022-10-12 36203093 Hakkaart C 2022-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36203093 Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers. Breast cancer in BRCA2 pathogenic variant carriers (CNV deletions) 5,488 European ancestry cases, 5,252 European ancestry controls NA Illumina [16395] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90134569 Genome-wide genotyping array 2022-10-12 36203093 Hakkaart C 2022-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36203093 Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers. Breast cancer in BRCA2 pathogenic variant carriers (CNV duplications) 5,488 European ancestry cases, 5,252 European ancestry controls NA Illumina [16395] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90134570 Genome-wide genotyping array 2022-08-18 35589863 Gouveia C 2022-05-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35589863 Genome-wide association of polygenic risk extremes for Alzheimer's disease in the UK Biobank. Alzheimer’s disease polygenic risk score (upper quantile vs lower quantile) 18,892 European ancestry high risk individuals, 18,892 European ancestry low risk individuals NA NR [NR] 477 Alzheimer disease, polygenic risk score http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0030082 GCST90132260 Genome-wide genotyping array 2022-10-05 35953715 Mathur R 2022-08-11 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35953715 GAWMerge expands GWAS sample size and diversity by combining array-based genotyping and whole-genome sequencing. Chronic obstructive pulmonary disease 4,500 European ancestry cases, 4,436 European ancestry controls, 813 African American cases, 712 African American controls NA Illumina [NR] (imputed) 5 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90162551 Genome-wide genotyping array, Genome-wide sequencing 2022-08-19 35611668 Lee HW 2022-05-25 Gut Liver www.ncbi.nlm.nih.gov/pubmed/35611668 Impact of Evolutionary Changes in Nonalcoholic Fatty Liver Disease on Lung Function Decline. Accelerated lung function decline (FVC) and worsened/persistent change in fatty liver (pleiotropy) 1,018 East Asian ancestry cases with worsened or persistent steatosis and accelerated lung function decline rates, 1,803 East Asian ancestry controls with normal or improved steatosis and slow lung function decline rates NA NR [NR] (imputed) 6 FVC change measurement, fatty liver disease http://www.ebi.ac.uk/efo/EFO_0010339, http://purl.obolibrary.org/obo/MONDO_0004790 GCST90132296 Genome-wide genotyping array 2022-08-19 35611668 Lee HW 2022-05-25 Gut Liver www.ncbi.nlm.nih.gov/pubmed/35611668 Impact of Evolutionary Changes in Nonalcoholic Fatty Liver Disease on Lung Function Decline. Accelerated lung function decline (FEV1) and worsened/persistent change in fatty liver (pleiotropy) 951 East Asian ancestry cases with worsened or persistent steatosis and accelerated lung function decline rates, 1,771 East Asian ancestry controls with normal or improved steatosis and slow lung function decline rates NA NR [NR] (imputed) 7 FEV change measurement, fatty liver disease http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/MONDO_0004790 GCST90132297 Genome-wide genotyping array 2022-10-18 34865855 Maihofer AX 2021-09-28 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34865855 Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. Post-traumatic stress disorder 182,199 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 6 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90095185 Genome-wide genotyping array 2022-10-18 34865855 Maihofer AX 2021-09-28 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34865855 Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. Trauma exposure 132,988 European ancestry individuals NA Affymetrix [NR] (imputed) 6 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST90095186 Genome-wide genotyping array 2022-10-18 34865855 Maihofer AX 2021-09-28 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34865855 Enhancing Discovery of Genetic Variants for Posttraumatic Stress Disorder Through Integration of Quantitative Phenotypes and Trauma Exposure Information. Post-traumatic stress disorder (MTAG) 217,491 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 10 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90095187 Genome-wide genotyping array 2022-10-03 34426670 Merino J 2021-08-23 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34426670 Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits. Relative carbohydrate intake 282,271 European ancestry individuals NA Affymetrix [11800000] (imputed) 11 carbohydrate intake measurement http://www.ebi.ac.uk/efo/EFO_0010811 GCST90032648 Genome-wide genotyping array 2022-10-03 34426670 Merino J 2021-08-23 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34426670 Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits. Relative fat intake 282,271 European ancestry individuals NA Affymetrix [11800000] (imputed) 12 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90032649 Genome-wide genotyping array 2022-10-03 34426670 Merino J 2021-08-23 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34426670 Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits. Relative protein intake 282,271 European ancestry individuals NA Affymetrix [11800000] (imputed) 9 protein intake measurement http://www.ebi.ac.uk/efo/EFO_0010810 GCST90032650 Genome-wide genotyping array 2022-10-03 34426670 Merino J 2021-08-23 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34426670 Genetic analysis of dietary intake identifies new loci and functional links with metabolic traits. Dietary macronutrient intake (multi-trait analysis) 282,271 European ancestry individuals NA Affymetrix [11800000] (imputed) 35 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90032651 Genome-wide genotyping array 2022-09-05 35764056 Rao S 2022-06-28 Neuropsychobiology www.ncbi.nlm.nih.gov/pubmed/35764056 Genetic Relationships between Attention-Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, and Intelligence. Attention deficit hyperactivity disorder or autism spectrum disorder or intelligence (pleiotropy) 20,183 European ancestry ADHD cases, 18,381 European ancestry ASD cases, up to 63,160 European ancestry controls, 269,867 European ancestry individuals with intelligence measurements NA NR [6307410] (imputed) 486 attention deficit hyperactivity disorder, autism spectrum disorder, intelligence http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003756, http://www.ebi.ac.uk/efo/EFO_0004337 GCST90134330 Genome-wide genotyping array 2022-10-31 36215317 Sabino EC 2022-10-10 PLoS Negl Trop Dis www.ncbi.nlm.nih.gov/pubmed/36215317 Genome-wide association study for Chagas Cardiomyopathy identify a new risk locus on chromosome 18 associated with an immune-related protein and transcriptional signature. Chronic Chagas Cardiomyopathy in Chagas disease 2,383 European ancestry cases, 581 European ancestry controls NA Affymetrix [12457719] (imputed) 11 Chagas cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0005529 GCST90104564 Genome-wide genotyping array 2022-08-31 35727948 Gehlen J 2022-06-21 Cardiovasc Res www.ncbi.nlm.nih.gov/pubmed/35727948 Elucidation of the genetic causes of bicuspid aortic valve disease. Bicuspid aortic valve 2,236 European ancestry cases, 11,604 European ancestry controls 421 European ancestry cases, 3,643 European ancestry controls Illumina [NR] (imputed) 3 Bicuspid aortic valve http://purl.obolibrary.org/obo/HP_0001647 GCST90133377 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Height (population-based) upto 71,108 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90133114 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Body mass index (population-based) upto 71,108 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90133115 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Educational attainment (population-based) upto 64,053 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90133116 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Ever smoked (population-based) upto 61,421 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90133117 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Systolic blood pressure (population-based) upto 57,702 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90133118 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Waist-hip ratio (population-based) upto 48,364 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90133119 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Alcohol consumption (population-based) upto 51,894 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90133120 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Age at menarche (population-based) upto 42,403 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90133121 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Age at first birth (population-based) upto 54,318 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST90133122 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Number of children ever born (population-based) upto 57,482 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90133123 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Ever smoked (within-sibship) upto 61,421 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90133141 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Cognition (population-based) upto 34,534 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90133125 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Waist-hip ratio (within-sibship) upto 48,364 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90133143 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Neuroticism (population-based) upto 52,161 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90133127 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Age at menarche (within-sibship) upto 42,403 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90133145 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Cigarettes smoked per day (population-based) upto 52,595 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90133129 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Number of children ever born (within-sibship) upto 57,482 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90133147 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. HDL cholesterol levels (population-based) upto 52,110 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90133131 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Cognition (within-sibship) upto 34,534 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90133149 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. C-reactive protein levels (population-based) upto 43,753 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90133133 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Neuroticism (within-sibship) upto 52,161 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90133151 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Lung function (population-based) upto 39,963 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90133135 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Subjective well-being (population-based) upto 54,165 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90133136 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Hemoglobin A1c levels (population-based) upto 38,170 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90133137 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Height (within-sibship) upto 71,108 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90133138 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Triglyceride levels (within-sibship) upto 47,943 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90133156 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. C-reactive protein levels (within-sibship) upto 43,753 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90133157 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Estimated glomerular filtration rate (within-sibship) upto 39,674 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90133158 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Lung function (within-sibship) upto 39,963 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90133159 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Subjective well-being (within-sibship) upto 54,165 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90133160 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Hemoglobin A1c levels (within-sibship) upto 38,170 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90133161 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Body mass index (within-sibship) upto 71,108 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90133139 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Educational attainment (within-sibship) upto 64,053 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90133140 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Age at menopause (population-based) upto 36,760 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90133124 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Systolic blood pressure (within-sibship) upto 57,702 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90133142 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Depressive symptoms (population-based) upto 31,994 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90133126 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Alcohol consumption (within-sibship) upto 51,894 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90133144 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Physical activity (population-based) upto 47,357 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90133128 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Age at first birth (within-sibship) upto 54,318 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST90133146 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. LDL cholesterol levels (population-based) upto 44,461 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90133130 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Age at menopause (within-sibship) upto 36,760 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90133148 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Triglyceride levels (population-based) upto 47,943 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90133132 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Depressive symptoms (within-sibship) upto 31,994 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90133150 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Estimated glomerular filtration rate (population-based) upto 39,674 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90133134 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Physical activity (within-sibship) upto 47,357 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90133152 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. Cigarettes smoked per day (within-sibship) upto 52,595 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90133153 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. LDL cholesterol levels (within-sibship) upto 44,461 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90133154 Genome-wide genotyping array 2022-08-26 35534559 Howe LJ 2022-05-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35534559 Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. HDL cholesterol levels (within-sibship) upto 52,110 European ancestry sibship NA Affymetrix, Illumina [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90133155 Genome-wide genotyping array 2023-02-22 35507331 Soomro M 2022-05-04 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/35507331 Comparative genetic analysis of psoriatic arthritis and psoriasis for the discovery of genetic risk factors and risk prediction modelling. Psoriatic arthritis 5,065 European ancestry cases, 21,286 European ancestry controls NA Illumina [8558403] (imputed) 13 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90243956 Genome-wide genotyping array 2023-02-22 35507331 Soomro M 2022-05-04 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/35507331 Comparative genetic analysis of psoriatic arthritis and psoriasis for the discovery of genetic risk factors and risk prediction modelling. Psoriatic arthritis vs Cutaneous psoriasis 4,340 European ancestry psoriatic arthritis cases, 6,431 European ancestry cutaneous arthritis cases NA Illumina [NR] (imputed) 4 psoriatic arthritis, psoriasis http://www.ebi.ac.uk/efo/EFO_0003778, http://www.ebi.ac.uk/efo/EFO_0000676 GCST90243957 Genome-wide genotyping array 2022-09-28 34319147 Choi SH 2021-07-28 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34319147 Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis. RR interval 5,034 African American individuals, 615 admixed American individuals, 17,777 European ancestry individuals, 727 East Asian ancestry individuals, 56 South Asian ancestry individuals, 3,758 individuals NA NR [294000000] 6 RR interval http://www.ebi.ac.uk/efo/EFO_0004831 GCST90093372 Genome-wide sequencing 2022-09-28 34319147 Choi SH 2021-07-28 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34319147 Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis. P wave duration 4,149 African American individuals, 520 admixed American individuals, 15,801 European ancestry individuals, 700 East Asian ancestry individuals, 2,397 individuals NA NR [294000000] 6 P wave duration http://www.ebi.ac.uk/efo/EFO_0005094 GCST90093373 Genome-wide sequencing 2022-09-28 34319147 Choi SH 2021-07-28 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34319147 Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis. PR interval 5,063 African American individuals, 616 admixed American individuals, 17,731 European ancestry individuals, 727 East Asian ancestry individuals, 57 South Asian ancestry individuals, 3,814 individuals 29,629 European or unknown ancestry individuals NR [294000000] 0 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST90093374 Genome-wide sequencing 2022-09-28 34319147 Choi SH 2021-07-28 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34319147 Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis. QRS duration 5,019 African American individuals, 610 admixed American individuals, 17,669 European ancestry individuals, 727 East Asian ancestry individuals, 57 South Asian ancestry individuals, 3,792 individuals 11,356 European ancestry individuals NR [294000000] 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90093375 Genome-wide sequencing 2022-09-28 34319147 Choi SH 2021-07-28 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34319147 Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis. QTc interval 4,887 African American individuals, 596 admixed American individuals, 17,072 European ancestry individuals, 715 East Asian ancestry individuals, 53 South Asian ancestry individuals, 3,653 individuals NA NR [294000000] 9 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90093376 Genome-wide sequencing 2022-08-26 35688625 Allen RJ 2022-06-10 Thorax www.ncbi.nlm.nih.gov/pubmed/35688625 Genome-wide association study across five cohorts identifies five novel loci associated with idiopathic pulmonary fibrosis. Idiopathic pulmonary fibrosis 4,125 European ancestry cases, 20,464 European ancestry controls NA Illumina [7554248] (imputed) 23 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST90133317 Genome-wide genotyping array 2022-08-24 35754128 Herrera-Luis E 2022-06-01 Pediatr Allergy Immunol www.ncbi.nlm.nih.gov/pubmed/35754128 Multi-ancestry genome-wide association study of asthma exacerbations. Asthma exacerbations 1,007 European ancestry cases, 3,982 European ancestry controls, 43 East Asian ancestry cases, 1,207 East Asian ancestry controls, 1,283 Hispanic or Latin American cases, 898 Hispanic or Latin American controls, 448 African American cases, 524 African American controls 3,030 European ancestry cases, 34,525 European ancestry controls, 375 Latino cases, 502 Latino controls, 27 Filipino ancestry cases, 174 Filipino ancestry controls Affymetrix, Illumina [9634748] (imputed) 4 asthma exacerbation measurement http://www.ebi.ac.uk/efo/EFO_0007614 GCST90132627 Genome-wide genotyping array 2022-08-25 35927272 Chang X 2022-05-02 NPJ Aging www.ncbi.nlm.nih.gov/pubmed/35927272 Genetic associations with healthy ageing among Chinese adults. Healthy aging 1,489 Chinese ancestry cases, 5,721 Chinese ancestry controls 129 Chinese ancestry cases, 500 Chinese ancestry controls Illumina [NR] (imputed) 25 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90132317 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Geographic atrophy within a central 5 mm circle (model 1) 1,074 Amish individuals NA Illumina [831296] 6 atrophic macular degeneration http://www.ebi.ac.uk/efo/EFO_1001492 GCST90132232 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen area within a central 5 mm circle (model 1) 1,074 Amish individuals NA Illumina [831296] 9 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132233 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen volume within a central 5 mm circle (model 1) 1,074 Amish individuals NA Illumina [831296] 7 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132234 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen area within a central 3 mm circle (model 1) 1,074 Amish individuals NA Illumina [831296] 7 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132235 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen volume within a central 3 mm circle (model 1) 1,074 Amish individuals NA Illumina [831296] 6 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132236 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Geographic atrophy within a central 5 mm circle (model 2) 59 Amish individuals NA Illumina [831296] 0 atrophic macular degeneration http://www.ebi.ac.uk/efo/EFO_1001492 GCST90132237 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen area within a central 5 mm circle (model 2) 226 Amish individuals NA Illumina [831296] 3 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132238 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen volume within a central 5 mm circle (model 2) 166 Amish individuals NA Illumina [831296] 4 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132239 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen area within a central 3 mm circle (model 2) 182 Amish individuals NA Illumina [831296] 2 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132240 Genome-wide genotyping array 2022-08-19 35857289 Osterman MD 2022-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/35857289 Genomewide Association Study of Retinal Traits in the Amish Reveals Loci Influencing Drusen Development and Link to Age-Related Macular Degeneration. Drusen volume within a central 3 mm circle (model 2) 131 Amish individuals NA Illumina [831296] 12 retinal drusen http://www.ebi.ac.uk/efo/EFO_1001155 GCST90132241 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (agents acting on the renin-angiotensin system) 62,752 European ancestry cases, 174,778 European ancestry controls, 45,820 East Asian ancestry cases, 132,906 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 171 Agents acting on the renin-angiotensin system use measurement http://www.ebi.ac.uk/efo/EFO_0009931 GCST90018988 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (HMG CoA reductase inhibitors) 73,475 European ancestry cases, 216,910 European ancestry controls, 33,295 East Asian ancestry cases, 145,431 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 94 HMG CoA reductase inhibitor use measurement http://www.ebi.ac.uk/efo/EFO_0009932 GCST90018989 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (thyroid preparations) 24,832 European ancestry cases, 280,750 European ancestry controls, 3,103 East Asian ancestry cases, 175,623 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 118 Thyroid preparation use measurement http://www.ebi.ac.uk/efo/EFO_0009933 GCST90018990 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (immunosuppressants) 3,954 European ancestry cases, 268,648 European ancestry controls, 3,483 East Asian ancestry cases, 175,243 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 7 Immunosuppressant use measurement http://www.ebi.ac.uk/efo/EFO_0009934 GCST90018991 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (anti-inflammatory and antirheumatic products, non-steroids) 74,150 European ancestry cases, 90,370 European ancestry controls, 29,694 East Asian ancestry cases, 149,032 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 4 Non-steroidal anti-inflammatory and antirheumatic product use measurement http://www.ebi.ac.uk/efo/EFO_0009935 GCST90018992 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (drugs affecting bone structure and mineralization) 7,870 European ancestry cases, 207,798 European ancestry controls, 6,143 East Asian ancestry cases, 172,583 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 14 Drugs affecting bone structure and mineralization use measurement http://www.ebi.ac.uk/efo/EFO_0009936 GCST90018993 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (opioids) 22,982 European ancestry cases, 55,826 European ancestry controls, 3,566 East Asian ancestry cases, 175,160 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 2 Opioid use measurement http://www.ebi.ac.uk/efo/EFO_0009937 GCST90018994 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (salicylic acid and derivatives) 61,583 European ancestry cases, 50,427 European ancestry controls, 41,461 East Asian ancestry cases, 137,265 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 24 aspirin use measurement http://www.ebi.ac.uk/efo/EFO_0007013 GCST90018995 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (anilides) 83,218 European ancestry cases, 96,592 European ancestry controls, 4,421 East Asian ancestry cases, 174,305 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 7 Anilide use measurement http://www.ebi.ac.uk/efo/EFO_0009938 GCST90018996 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antimigraine preparations) 5,521 European ancestry cases, 114,323 European ancestry controls, 387 East Asian ancestry cases, 178,339 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 12 Antimigraine preparation use measurement http://www.ebi.ac.uk/efo/EFO_0009939 GCST90018997 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antidepressants) 33,757 European ancestry cases, 270,405 European ancestry controls, 3,288 East Asian ancestry cases, 175,438 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 1 Antidepressant use measurement http://www.ebi.ac.uk/efo/EFO_0009940 GCST90018998 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (adrenergics, inhalants) 28,880 European ancestry cases, 147,565 European ancestry controls, 5,880 East Asian ancestry cases, 172,846 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 49 Inhalant adrenergic use measurement http://www.ebi.ac.uk/efo/EFO_0009941 GCST90018999 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (glucocorticoids) 17,352 European ancestry cases, 188,348 European ancestry controls, 13,102 East Asian ancestry cases, 165,624 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 25 Glucocorticoid use measurement http://www.ebi.ac.uk/efo/EFO_0009942 GCST90019000 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antihistamines for systemic use) 13,984 European ancestry cases, 137,652 European ancestry controls, 10,163 East Asian ancestry cases, 168,563 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 8 Antihistamine use measurement http://www.ebi.ac.uk/efo/EFO_0009943 GCST90019001 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antiglaucoma preparations and miotics) 5,215 European ancestry cases, 95,653 European ancestry controls, 5,911 East Asian ancestry cases, 172,815 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 15 Antiglaucoma preparations and miotics use measurement http://www.ebi.ac.uk/efo/EFO_0009944 GCST90019002 Genome-wide genotyping array 2022-12-02 35933036 Zhang L 2022-08-03 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/35933036 Genome-wide association study of chronic spontaneous urticaria reveals genetic overlap with autoimmune diseases, not atopic diseases. Chronic spontaneous urticaria 430 Han Chinese ancestry cases, 482 Han Chinese ancestry controls 800 Han Chinese ancestry cases, 900 Han Chinese ancestry controls Illumina [5096893] (imputed) 8 urticaria http://www.ebi.ac.uk/efo/EFO_0005531 GCST90104038 Genome-wide genotyping array 2023-02-24 36691909 Liu Z 2023-01-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/36691909 Deep learning identified genetic variants for COVID-19-related mortality among 28,097 affected cases in UK Biobank. Mortality in COVID-19 1,104 British ancestry cases, 17,627 British ancestry controls NA NR [8200000] (imputed) 1 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90250895 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Otitis media 2,434 European ancestry cases, 12,170 European ancestry controls NA Illumina [8609082] (imputed) 1 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST90225535 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Chronic sinus infection 2,572 European ancestry cases, 12,860 European ancestry controls NA Illumina [8533812] (imputed) 0 susceptibility to chronic sinus infection measurement http://www.ebi.ac.uk/efo/EFO_0008419 GCST90225536 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Cold sores 356 European ancestry cases, 3,560 European ancestry controls NA Illumina [8575753] (imputed) 0 susceptibility to cold sores measurement http://www.ebi.ac.uk/efo/EFO_0008402 GCST90225537 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Hepatitis B 223 European ancestry cases, 2,230 European ancestry controls NA Illumina [8554291] (imputed) 0 hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004197 GCST90225538 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Hepatitis C 1,260 European ancestry cases, 6,300 European ancestry controls NA Illumina [8562888] (imputed) 0 hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0003047 GCST90225539 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Mononucleosis 116 European ancestry cases, 1,160 European ancestry controls NA Illumina [8732436] (imputed) 0 infectious mononucleosis http://www.ebi.ac.uk/efo/EFO_0007326 GCST90225540 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Pneumonia 6,385 European ancestry cases, 31,925 European ancestry controls NA Illumina [8490398] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90225541 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Tuberculosis 102 European ancestry cases, 1,020 European ancestry controls NA Illumina [8620585] (imputed) 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90225542 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Herpes zoster 751 European ancestry cases, 7,510 European ancestry controls NA Illumina [8534315] (imputed) 0 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST90225543 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Streptococcal pharyngitis 997 European ancestry cases, 9,970 European ancestry controls NA Illumina [8621211] (imputed) 0 streptococcal pharyngitis http://www.ebi.ac.uk/efo/EFO_1002024 GCST90225544 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Urinary tract infection 9,359 European ancestry cases, 46,795 European ancestry controls NA Illumina [8466962] (imputed) 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90225545 Genome-wide genotyping array 2022-11-14 36167494 Jiang L 2022-09-27 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36167494 Genome-wide association analyses of common infections in a large practice-based biobank. Candidiasis 2,202 European ancestry cases, 11,010 European ancestry controls NA Illumina [8553445] (imputed) 1 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90225546 Genome-wide genotyping array 2022-08-04 35538205 Wang SH 2022-05-10 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/35538205 Causality of abdominal obesity on cognition: a trans-ethnic Mendelian randomization study. Waist-to-hip ratio adjusted for BMI 65,683 Asian ancestry individuals NA Affymetrix [NR] (imputed) 20 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90131908 Genome-wide genotyping array 2022-08-04 35538205 Wang SH 2022-05-10 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/35538205 Causality of abdominal obesity on cognition: a trans-ethnic Mendelian randomization study. Global cognition (Mini Mental State Examination) 21,273 Asian ancestry individuals NA Affymetrix [NR] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90131909 Genome-wide genotyping array 2022-08-04 35538205 Wang SH 2022-05-10 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/35538205 Causality of abdominal obesity on cognition: a trans-ethnic Mendelian randomization study. Body mass index 65,689 Asian ancestry individuals NA Affymetrix [NR] (imputed) 26 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90131907 Genome-wide genotyping array 2022-09-20 35990758 Ramadan FA 2022-08-02 BMJ Open Sport Exerc Med www.ncbi.nlm.nih.gov/pubmed/35990758 Association of sedentary and physical activity behaviours with body composition: a genome-wide association and Mendelian randomisation study. Moderate physical activity 360,911 European ancestry individuals NA NR [NR] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90134665 Genome-wide genotyping array 2022-09-20 35990758 Ramadan FA 2022-08-02 BMJ Open Sport Exerc Med www.ncbi.nlm.nih.gov/pubmed/35990758 Association of sedentary and physical activity behaviours with body composition: a genome-wide association and Mendelian randomisation study. Accelerometer measured moderate to vigorous physical activity 97,737 European ancestry individuals NA NR [NR] (imputed) 2 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90134666 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Cardioembolic stroke 926 East Asian ancestry cases, 237,242 East Asian ancestry controls NA Affymetrix, Illumina [5169601] (imputed) 0 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90104546 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Cardioembolic stroke 10,804 European ancestry cases, 1,234,808 European ancestry controls NA Affymetrix, Illumina [6659794] (imputed) 6 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90104541 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Cardioembolic stroke 223 Hispanic cases, 4,146 Hispanic controls NA Affymetrix, Illumina [7404873] (imputed) 0 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90104556 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Cardioembolic stroke 596 South Asian ancestry cases, 7,672 South Asian ancestry controls NA Affymetrix, Illumina [3936847] (imputed) 0 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90104561 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Small vessel stroke 423 African American cases, 20,030 African American controls NA Affymetrix, Illumina [5298687] (imputed) 1 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90104553 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke 213 African American cases, 20,030 African American controls, 1,735 East Asian ancestry cases, 237,242 East Asian ancestry controls, 6,399 European ancestry cases, 1,234,808 European ancestry controls, 167 Hispanic cases, 4,146 Hispanic controls, 705 South Asian ancestry cases, 7,672 South Asian ancestry controls NA Affymetrix, Illumina [5980001] (imputed) 3 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90104538 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Small vessel stroke 5,532 East Asian ancestry cases, 237,242 East Asian ancestry controls NA Affymetrix, Illumina [5993006] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90104548 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Small vessel stroke 6,811 European ancestry cases, 1,234,808 European ancestry controls NA Affymetrix, Illumina [5784789] (imputed) 3 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90104543 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Small vessel stroke 207 Hispanic cases, 4,146 Hispanic controls NA Affymetrix, Illumina [7176984] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90104558 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Small vessel stroke 647 South Asian ancestry cases, 7,672 South Asian ancestry controls NA Affymetrix, Illumina [3864188] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90104563 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke 213 African American cases, 20,030 African American controls NA Affymetrix, Illumina [5259725] (imputed) 0 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90104552 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Small vessel stroke 423 African American cases, 20,030 African American controls, 5,532 East Asian ancestry cases, 237,242 East Asian ancestry controls, 6,811 European ancestry cases, 1,234,808 European ancestry controls, 207 Hispanic cases, 4,146 Hispanic controls, 647 South Asian ancestry cases, 7,672 South Asian ancestry controls NA Affymetrix, Illumina [6395566] (imputed) 5 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90104537 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke 1,735 East Asian ancestry cases, 237,242 East Asian ancestry controls NA Affymetrix, Illumina [6173638] (imputed) 0 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90104547 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke 6,399 European ancestry cases, 1,234,808 European ancestry controls NA Affymetrix, Illumina [5974029] (imputed) 4 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90104542 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke 167 Hispanic cases, 4,146 Hispanic controls NA Affymetrix, Illumina [7357893] (imputed) 0 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90104557 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke 705 South Asian ancestry cases, 7,672 South Asian ancestry controls NA Affymetrix, Illumina [3803264] (imputed) 0 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90104562 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Cardioembolic stroke (MTAG) 10,804 European ancestry cases, 1,234,808 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 6 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90162543 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke (MTAG) 6,399 European ancestry cases, 1,234,808 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 15 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90162544 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Large artery stroke (MTAG) 5,532 East Asian ancestry cases, 237,242 East Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 1 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90162545 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Small vessel stroke (MTAG) 6,811 European ancestry cases, 1,234,808 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 5 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90162546 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Ischemic stroke 894 African American cases, 20,030 African American controls 13,709 African ancestry cases, 124,346 African ancestry controls Affymetrix, Illumina [8357163] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90104550 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Ischemic stroke 894 African American cases, 20,030 African American controls, 19,032 East Asian ancestry cases, 237,242 East Asian ancestry controls, 62,100 European ancestry cases, 1,234,808 European ancestry controls, 1,180 Hispanic cases, 4,146 Hispanic controls, 3,462 South Asian ancestry cases, 7,672 South Asian ancestry controls 13,709 African ancestry cases, 124,346 African ancestry controls, 8,304 East Asian ancestry cases, 174,855 East Asian ancestry controls, 59,911 European ancestry cases, 665,176 European ancestry controls, 3,522 Hispanic cases, 49,323 Hispanic controls, 100 South Asian ancestry cases, 143 South Asian ancestry controls Affymetrix, Illumina [7407884] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90104535 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Ischemic stroke 19,032 East Asian ancestry cases, 237,242 East Asian ancestry controls 8,304 East Asian ancestry cases, 174,855 East Asian ancestry controls Affymetrix, Illumina [6725217] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90104545 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Ischemic stroke 62,100 European ancestry cases, 1,234,808 European ancestry controls 59,911 European ancestry cases, 665,176 European ancestry controls Affymetrix, Illumina [7482033] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90104540 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Ischemic stroke 1,180 Hispanic cases, 4,146 Hispanic controls 3,522 Hispanic cases, 49,323 Hispanic controls Affymetrix, Illumina [7277674] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90104555 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Ischemic stroke 3,462 South Asian ancestry cases, 7,672 South Asian ancestry controls 100 South Asian ancestry cases, 143 South Asian ancestry controls Affymetrix, Illumina [3306954] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90104560 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Stroke 3,961 African American cases, 20,030 African American controls 13,903 African ancestry cases, 124,346 African ancestry controls Affymetrix, Illumina [10831841] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90104549 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Stroke 3,961 African American cases, 20,030 African American controls, 27,413 East Asian ancestry cases, 237,242 East Asian ancestry controls, 73,652 European ancestry cases, 1,234,808 European ancestry controls, 1,516 Hispanic cases, 4,146 Hispanic controls, 3,640 South Asian ancestry cases, 7,672 South Asian ancestry controls 13,903 African ancestry cases, 124,346 African ancestry controls, 9,038 East Asian ancestry cases, 174,855 East Asian ancestry controls, 62,395 European ancestry cases, 665,176 European ancestry controls, 3,634 Hispanic cases, 49,323 Hispanic controls, 114 South Asian ancestry cases, 143 South Asian ancestry controls Affymetrix, Illumina [7588359] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90104534 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Stroke 27,413 East Asian ancestry cases, 237,242 East Asian ancestry controls 9,038 East Asian ancestry cases, 174,855 East Asian ancestry controls Affymetrix, Illumina [6789910] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90104544 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Stroke 73,652 European ancestry cases, 1,234,808 European ancestry controls 62,395 European ancestry cases, 665,176 European ancestry controls Affymetrix, Illumina [7511477] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90104539 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Stroke 1,516 Hispanic cases, 4,146 Hispanic controls 3,634 Hispanic cases, 49,323 Hispanic controls Affymetrix, Illumina [7718819] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90104554 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Stroke 3,640 South Asian ancestry cases, 7,672 South Asian ancestry controls 114 South Asian ancestry cases, 143 South Asian ancestry controls Affymetrix, Illumina [3306957] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90104559 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Cardioembolic stroke 241 African American cases, 20,030 African American controls NA Affymetrix, Illumina [6635546] (imputed) 0 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90104551 Genome-wide genotyping array 2023-02-22 36180795 Mishra A 2022-09-30 Nature www.ncbi.nlm.nih.gov/pubmed/36180795 Stroke genetics informs drug discovery and risk prediction across ancestries. Cardioembolic stroke 241 African American cases, 20,030 African American controls, 926 East Asian ancestry cases, 237,242 East Asian ancestry controls, 10,804 European ancestry cases, 1,234,808 European ancestry controls, 223 Hispanic cases, 4,146 Hispanic controls, 596 South Asian ancestry cases, 7,672 South Asian ancestry controls NA Affymetrix, Illumina [6614654] (imputed) 6 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90104536 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Eukaryotic translation initiation factor 4E-binding protein 1 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958024] (imputed) 0 level of eukaryotic translation initiation factor 4E-binding protein 1 in blood plasma http://purl.obolibrary.org/obo/OBA_2050337 GCST90274758 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Adenosine Deaminase levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958021] (imputed) 1 adenosine deaminase measurement http://www.ebi.ac.uk/efo/EFO_0010761 GCST90274759 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Artemin levels 11,778 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12685331] (imputed) 0 artemin measurement http://www.ebi.ac.uk/efo/EFO_0020162 GCST90274760 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Axin-1 levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687024] (imputed) 0 axin-1 measurement http://www.ebi.ac.uk/efo/EFO_0010763 GCST90274761 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. beta-nerve growth factor levels 14,743 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958290] (imputed) 0 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST90274762 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Caspase 8 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958301] (imputed) 0 caspase-8 measurement http://www.ebi.ac.uk/efo/EFO_0010764 GCST90274763 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Eotaxin levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957206] (imputed) 5 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90274764 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-C motif chemokine 19 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957400] (imputed) 4 C-C motif chemokine 19 measurement http://www.ebi.ac.uk/efo/EFO_0008047 GCST90274765 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-C motif chemokine 20 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958026] (imputed) 0 C-C motif chemokine 20 measurement http://www.ebi.ac.uk/efo/EFO_0010910 GCST90274766 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-C motif chemokine 23 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957980] (imputed) 1 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90274767 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-C motif chemokine 25 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958021] (imputed) 3 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90274768 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-C motif chemokine 28 levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957480] (imputed) 0 C-C motif chemokine 28 measurement http://www.ebi.ac.uk/efo/EFO_0020199 GCST90274769 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-C motif chemokine 4 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958254] (imputed) 2 C-C motif chemokine 4-like measurement http://www.ebi.ac.uk/efo/EFO_0021848 GCST90274770 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Natural killer cell receptor 2B4 levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957958] (imputed) 2 natural killer cell receptor 2B4 measurement http://www.ebi.ac.uk/efo/EFO_0021882 GCST90274771 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. CD40L receptor levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958023] (imputed) 1 CD40 measurement http://www.ebi.ac.uk/efo/EFO_0010586 GCST90274772 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. T-cell surface glycoprotein CD5 levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957995] (imputed) 1 t-cell surface glycoprotein CD5 measurement http://www.ebi.ac.uk/efo/EFO_0803134 GCST90274773 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. T-cell surface glycoprotein CD6 isoform levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957572] (imputed) 1 level of T-cell differentiation antigen CD6 in blood plasma http://purl.obolibrary.org/obo/OBA_2050336 GCST90274774 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. CUB domain-containing protein 1 levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957401] (imputed) 3 CUB domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802432 GCST90274775 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Macrophage colony-stimulating factor 1 levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957362] (imputed) 0 macrophage colony-stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020546 GCST90274776 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Cystatin D levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958010] (imputed) 4 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90274777 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Fractalkine levels 14,743 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957856] (imputed) 1 fractalkine measurement http://www.ebi.ac.uk/efo/EFO_0020395 GCST90274778 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-X-C motif chemokine 1 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958026] (imputed) 1 CXCL1 measurement http://www.ebi.ac.uk/efo/EFO_0010777 GCST90274779 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-X-C motif chemokine 10 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958296] (imputed) 2 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST90274780 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-X-C motif chemokine 11 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958024] (imputed) 4 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90274781 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-X-C motif chemokine 5 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958018] (imputed) 2 C-X-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008058 GCST90274782 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-X-C motif chemokine 6 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958279] (imputed) 1 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90274783 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. C-X-C motif chemokine 9 levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957464] (imputed) 1 C-X-C motif chemokine 9 measurement http://www.ebi.ac.uk/efo/EFO_0022032 GCST90274784 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Delta and Notch-like epidermal growth factor-related receptor levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957591] (imputed) 1 delta and Notch-like epidermal growth factor-related receptor measurement http://www.ebi.ac.uk/efo/EFO_0802458 GCST90274785 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Protein S100-A12 levels 14,743 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958213] (imputed) 1 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90274786 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Fibroblast growth factor 19 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958296] (imputed) 3 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90274787 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Fibroblast growth factor 21 levels 14,743 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957981] (imputed) 1 fibroblast growth factor 21 measurement http://www.ebi.ac.uk/efo/EFO_0010783 GCST90274788 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Fibroblast growth factor 23 levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957890] (imputed) 1 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90274789 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Fibroblast growth factor 5 levels 11,789 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12685639] (imputed) 1 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90274790 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Fms-related tyrosine kinase 3 ligand levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957312] (imputed) 1 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90274791 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Glial cell line-derived neurotrophic factor levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958018] (imputed) 1 glial cell line-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0021887 GCST90274792 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Hepatocyte growth factor levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957466] (imputed) 1 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90274793 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interferon gamma levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687006] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90274794 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-10 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958183] (imputed) 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90274795 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-10 receptor subunit alpha levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687028] (imputed) 0 interleukin-10 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0021890 GCST90274796 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-10 receptor subunit beta levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957474] (imputed) 1 interleukin-10 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020489 GCST90274797 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-12 subunit beta levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958012] (imputed) 7 obsolete_interleukin-12 subunit B measurement http://www.ebi.ac.uk/efo/EFO_0010787 GCST90274798 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-13 levels 11,792 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686926] (imputed) 0 interleukin-13 measurement http://www.ebi.ac.uk/efo/EFO_0802655 GCST90274799 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-15 receptor subunit alpha levels 11,792 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686578] (imputed) 1 interleukin-15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801716 GCST90274800 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-17A levels 11,784 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686079] (imputed) 0 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90274801 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-17C levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687025] (imputed) 0 interleukin-17C measurement http://www.ebi.ac.uk/efo/EFO_0802656 GCST90274802 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-18 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958301] (imputed) 2 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST90274803 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. interleukin-18 receptor 1 levels 14,743 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958280] (imputed) 2 interleukin-18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801721 GCST90274804 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-1-alpha levels 11,788 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12685920] (imputed) 0 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST90274805 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-2 levels 11,789 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12685297] (imputed) 0 interleukin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801723 GCST90274806 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-20 levels 11,784 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12685860] (imputed) 0 interleukin-20 measurement http://www.ebi.ac.uk/efo/EFO_0020496 GCST90274807 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MMP 7 plasma levels conditional to rs56857975 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 matrix metalloproteinase 7 measurement http://www.ebi.ac.uk/efo/EFO_0010591 GCST90085805 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MSP plasma levels conditional to rs11709525 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 macrophage-stimulating protein receptor measurement http://www.ebi.ac.uk/efo/EFO_0020550 GCST90085806 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. PARC plasma levels conditional to rs854469 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 C-C motif chemokine 18 measurement http://www.ebi.ac.uk/efo/EFO_0008046 GCST90085807 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. PON 1 plasma levels conditional to rs662 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 paraoxonase-1 measurement http://www.ebi.ac.uk/efo/EFO_0801085 GCST90085808 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. SP D plasma levels conditional to rs7072378 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 surfactant protein D measurement http://www.ebi.ac.uk/efo/EFO_0005081 GCST90085809 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. ST2 plasma levels conditional to rs11676124 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 ST2 protein measurement http://www.ebi.ac.uk/efo/EFO_0010599 GCST90085810 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. THP plasma levels conditional to rs9928003 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 urinary uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0005663 GCST90085811 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TIMP 3 plasma levels conditional to rs4821097 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 metalloproteinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008231 GCST90085812 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TN X plasma levels conditional to rs2856448 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90085813 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Vaspin plasma levels conditional to rs12434602 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 vaspin measurement http://www.ebi.ac.uk/efo/EFO_0004915 GCST90085814 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-20 receptor subunit alpha levels 11,792 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686362] (imputed) 0 interleukin-20 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020497 GCST90274808 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-22 receptor subunit alpha-1 levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687018] (imputed) 0 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90274809 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-24 levels 11,785 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686477] (imputed) 0 interleukin-24 measurement http://www.ebi.ac.uk/efo/EFO_0020502 GCST90274810 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-2 receptor subunit beta levels 11,792 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686983] (imputed) 0 interleukin-2 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0802657 GCST90274811 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-33 levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687027] (imputed) 0 level of interleukin-33 in blood plasma http://purl.obolibrary.org/obo/OBA_2050335 GCST90274812 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-4 levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687001] (imputed) 0 interleukin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802661 GCST90274813 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-5 levels 11,792 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686613] (imputed) 0 interleukin-5 measurement http://www.ebi.ac.uk/efo/EFO_0801729 GCST90274814 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-6 levels 14,743 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957771] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90274815 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-7 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958029] (imputed) 0 interleukin-7 measurement http://www.ebi.ac.uk/efo/EFO_0802662 GCST90274816 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Interleukin-8 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958300] (imputed) 0 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST90274817 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Latency-associated peptide transforming growth factor beta 1 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958007] (imputed) 1 transforming growth factor beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020780 GCST90274818 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Leukemia inhibitory factor levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687008] (imputed) 0 leukemia inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0801764 GCST90274819 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Leukemia inhibitory factor receptor levels 11,784 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686022] (imputed) 1 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90274820 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Monocyte chemoattractant protein-1 levels 14,733 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12956740] (imputed) 0 CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004749 GCST90274821 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Monocyte chemoattractant protein 2 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958020] (imputed) 0 monocyte chemotactic protein-2 measurement http://www.ebi.ac.uk/efo/EFO_0010789 GCST90274822 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Monocyte chemoattractant protein-3 levels 11,783 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12685212] (imputed) 0 monocyte chemotactic protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008235 GCST90274823 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Monocyte chemoattractant protein-4 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958013] (imputed) 0 monocyte chemotactic protein-4 measurement http://www.ebi.ac.uk/efo/EFO_0010790 GCST90274824 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Macrophage inflammatory protein 1a levels 14,743 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958177] (imputed) 1 macrophage inflammatory protein 1a measurement http://www.ebi.ac.uk/efo/EFO_0008218 GCST90274825 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Matrix metalloproteinase-1 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958289] (imputed) 3 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90274826 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Matrix metalloproteinase-10 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958280] (imputed) 2 matrix metalloproteinase 10 measurement http://www.ebi.ac.uk/efo/EFO_0010589 GCST90274827 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Neurturin levels 11,791 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686445] (imputed) 0 level of neurturin in blood plasma http://purl.obolibrary.org/obo/OBA_2050334 GCST90274828 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Neurotrophin-3 levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958282] (imputed) 1 neurotrophin-3 measurement http://www.ebi.ac.uk/efo/EFO_0010791 GCST90274829 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Osteoprotegerin levels 14,733 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957309] (imputed) 2 osteoprotegerin measurement http://www.ebi.ac.uk/efo/EFO_0005918 GCST90274830 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Oncostatin-M levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958020] (imputed) 2 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90274831 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Programmed cell death 1 ligand 1 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958024] (imputed) 1 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90274832 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Stem cell factor levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958021] (imputed) 6 stem Cell Factor measurement http://www.ebi.ac.uk/efo/EFO_0008291 GCST90274833 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. SIR2-like protein 2 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958022] (imputed) 0 SIR2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0010928 GCST90274834 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Signaling lymphocytic activation molecule levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957168] (imputed) 1 signaling lymphocytic activation molecule measurement http://www.ebi.ac.uk/efo/EFO_0803076 GCST90274835 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Sulfotransferase 1A1 levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687026] (imputed) 0 sulfotrasferase 1A1 measurement http://www.ebi.ac.uk/efo/EFO_0010797 GCST90274836 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. STAM binding protein levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958031] (imputed) 0 STAM binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010796 GCST90274837 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Transforming growth factor-alpha levels 14,733 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957586] (imputed) 0 transforming growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0010798 GCST90274838 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Tumor necrosis factor levels 11,785 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686484] (imputed) 0 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90274839 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. TNF-beta levels 11,792 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686475] (imputed) 2 lymphotoxin-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020544 GCST90274840 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Tumor necrosis factor receptor superfamily member 9 levels 11,784 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12686010] (imputed) 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90274841 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Tumor necrosis factor ligand superfamily member 14 levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687022] (imputed) 1 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90274842 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. TNF-related apoptosis-inducing ligand levels 14,735 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957573] (imputed) 3 TNF-related apoptosis-inducing ligand measurement http://www.ebi.ac.uk/efo/EFO_0008300 GCST90274843 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. TNF-related activation-induced cytokine levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958022] (imputed) 1 TNF-related activation-induced cytokine measurement http://www.ebi.ac.uk/efo/EFO_0010929 GCST90274844 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Thymic stromal lymphopoietin levels 11,793 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12687011] (imputed) 0 thymic stromal lymphopoietin measurement http://www.ebi.ac.uk/efo/EFO_0020772 GCST90274845 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Tumor necrosis factor ligand superfamily member 12 levels 14,736 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958021] (imputed) 1 tumor necrosis factor ligand superfamily member 12 measurement http://www.ebi.ac.uk/efo/EFO_0010801 GCST90274846 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Urokinase-type plasminogen activator levels 14,734 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12957460] (imputed) 5 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90274847 Genome-wide genotyping array 2023-08-21 37563310 Zhao JH 2023-08-10 Nat Immunol www.ncbi.nlm.nih.gov/pubmed/37563310 Genetics of circulating inflammatory proteins identifies drivers of immune-mediated disease risk and therapeutic targets. Vascular endothelial growth factor A levels 14,744 European ancestry individuals 1,585 European or unknown ancestry individuals Affymetrix, Illumina [12958279] (imputed) 3 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90274848 Genome-wide genotyping array 2023-01-13 36324510 Elghzaly AA 2022-10-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/36324510 Genome-wide association study for systemic lupus erythematosus in an egyptian population. Systemic lupus erythematosus 458 Egyptian ancestry cases, 769 Egyptian ancestry controls NA Illumina [6382276] (imputed) 9 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90244665 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Concentration of apixaban (at 3h) 181 Chinese ancestry individuals NA Affymetrix [NR] 4 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271717 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Concentration of apixaban (at 9h) 181 Chinese ancestry individuals NA Affymetrix [NR] 2 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271718 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Concentration of apixaban (at 12h) 181 Chinese ancestry individuals NA Affymetrix [NR] 17 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271719 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Peak concentration of apixaban 181 Chinese ancestry individuals NA Affymetrix [NR] 5 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271720 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Half-life of apixaban 181 Chinese ancestry individuals NA Affymetrix [NR] 24 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271721 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. AUC of apixaban 181 Chinese ancestry individuals NA Affymetrix [NR] 1 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271722 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Time to peak concentration of apixaban 181 Chinese ancestry individuals NA Affymetrix [NR] 3 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271723 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. anti-Xa activity of apixaban 181 Chinese ancestry individuals NA Affymetrix [NR] 24 trait in response to apixaban http://purl.obolibrary.org/obo/OBA_2050328 GCST90271724 Genome-wide genotyping array 2023-08-18 36867504 Mu G 2023-03-03 Expert Opin Drug Metab Toxicol www.ncbi.nlm.nih.gov/pubmed/36867504 Identification of genetic biomarkers associated with pharmacokinetics and pharmacodynamics of apixaban in Chinese healthy volunteers. Ratio of prothrombin after to before apixaban administration 181 Chinese ancestry individuals NA Affymetrix [NR] 1 trait in response to apixaban, prothrombin time measurement http://purl.obolibrary.org/obo/OBA_2050328, http://www.ebi.ac.uk/efo/EFO_0008390 GCST90271725 Genome-wide genotyping array 2022-11-22 36357561 Cervan-Martin M 2022-11-10 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36357561 Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Non-obstructive azoospermia 780 European ancestry cases, 1,951 European ancestry controls NA Illumina [7371432] (imputed) 0 azoospermia http://www.ebi.ac.uk/efo/EFO_0000279 GCST90239717 Genome-wide genotyping array 2022-11-22 36357561 Cervan-Martin M 2022-11-10 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36357561 Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Severe oligozoospermia 494 European ancestry cases, 1,951 European ancestry controls NA Illumina [7371432] (imputed) 0 azoospermia http://www.ebi.ac.uk/efo/EFO_0000279 GCST90239718 Genome-wide genotyping array 2022-11-22 36357561 Cervan-Martin M 2022-11-10 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36357561 Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Hypospermatogenesis 120 European ancestry cases, 1,951 European ancestry controls NA Illumina [7371432] (imputed) 0 GCST90239719 Genome-wide genotyping array 2022-11-22 36357561 Cervan-Martin M 2022-11-10 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36357561 Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Spermatogenic failure 1,274 European ancestry cases, 1,951 European ancestry controls NA Illumina [7371432] (imputed) 0 GCST90239716 Genome-wide genotyping array 2022-11-22 36357561 Cervan-Martin M 2022-11-10 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36357561 Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Male infertility (maturation arrest) 98 European ancestry cases, 1,951 European ancestry controls NA Illumina [7371432] (imputed) 0 GCST90239720 Genome-wide genotyping array 2022-11-22 36357561 Cervan-Martin M 2022-11-10 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36357561 Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Male infertility (Sertoli cell-only) 214 European ancestry cases, 1,951 European ancestry controls NA Illumina [7371432] (imputed) 2 Sertoli Cell-Only Syndrome http://www.ebi.ac.uk/efo/EFO_1001422 GCST90239721 Genome-wide genotyping array 2022-11-22 36357561 Cervan-Martin M 2022-11-10 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36357561 Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility. Unsuccessful sperm retrieval in biopsy 258 European ancestry cases, 1,951 European ancestry controls NA Illumina [7371432] (imputed) 1 GCST90239722 Genome-wide genotyping array 2023-08-11 36000784 Kulm S 2022-08-23 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/36000784 Characterization of Genetic Risk of End-Stage Knee Osteoarthritis Treated with Total Knee Arthroplasty: A Genome-Wide Association Study. End-stage knee osteoarthritis 16,032 European ancestry cases, 373,516 European ancestry controls NA NR [7833032] (imputed) 7 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90179469 Genome-wide genotyping array 2023-03-10 36539618 Fernandez-Rozadilla C 2022-12-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36539618 Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Colorectal cancer 21,731 European ancestry cases, 47,444 European ancestry controls, 78,473 East Asian ancestry cases, 107,143 East Asian ancestry controls NA Affymetrix, Illumina [22200000] (imputed) 189 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90129505 Genome-wide genotyping array 2023-03-10 36539618 Fernandez-Rozadilla C 2022-12-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36539618 Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Colorectal cancer 78,473 European ancestry cases, 107,143 European ancestry controls NA Affymetrix, Illumina [11284769] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90255675 Genome-wide genotyping array 2023-03-10 36539618 Fernandez-Rozadilla C 2022-12-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36539618 Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Colorectal cancer 73,673 European ancestry cases, 86,854 European ancestry controls NA Affymetrix, Illumina [10534518] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90255676 Genome-wide genotyping array 2023-03-10 36539618 Fernandez-Rozadilla C 2022-12-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36539618 Deciphering colorectal cancer genetics through multi-omic analysis of 100,204 cases and 154,587 controls of European and east Asian ancestries. Colorectal cancer 4,800 European ancestry cases, 20,289 European ancestry controls NA Affymetrix [8699506] (imputed) 0 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90255677 Genome-wide genotyping array 2022-11-23 35164939 van der Meer D 2022-02-11 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35164939 Boosting Schizophrenia Genetics by Utilizing Genetic Overlap With Brain Morphology. Brain morphology (MOSTest) 33,735 white British ancestry individuals NA NR [9061072] (imputed) 589 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90239729 Genome-wide genotyping array 2022-11-23 35164939 van der Meer D 2022-02-11 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35164939 Boosting Schizophrenia Genetics by Utilizing Genetic Overlap With Brain Morphology. Brain morphology or schizophrenia (pleiotropy) 33,735 white British ancestry individuals with neuroimaging measurements, 50,965 schizophrenia cases, 68,049 controls NA NR [NR] (imputed) 0 schizophrenia, neuroimaging measurement http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0004346 GCST90239730 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Alcohol dependence (codominant genetic model) 191 Russian ancestry cases, 1,017 Russian ancestry controls NA Illumina [411586] 8 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90245781 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Alcohol dependence (codominant genetic model) 26 Russian ancestry female cases, 194 Russian ancestry female controls NA Illumina [411586] 19 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90245782 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Alcohol dependence (codominant genetic model) 165 Russian ancestry male cases, 823 Russian ancestry male controls NA Illumina [411586] 4 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90245783 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Alcohol dependence (allelic genetic model) 165 Russian ancestry male cases, 823 Russian ancestry male controls NA Illumina [411586] 3 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90245784 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Alcohol dependence (dominant genetic model) 191 Russian ancestry cases, 1,017 Russian ancestry controls NA Illumina [411586] 2 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90245785 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Spielberger Trait Anxiety Inventory in alcohol dependence (allelic genetic model) 26 Russian ancestry women NA Illumina [381084] 1 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90245786 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Penn alcohol craving scale in alcohol dependence (codominant genetic model) 26 Russian ancestry women NA Illumina [381084] 1 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90245787 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Penn alcohol craving scale in alcohol dependence (allelic genetic model) 26 Russian ancestry women NA Illumina [381084] 1 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90245788 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Penn alcohol craving scale in alcohol dependence (recessive genetic model) 192 Russian ancestry individuals NA Illumina [381084] 2 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90245789 Genome-wide genotyping array 2023-01-30 36551763 Levchenko A 2022-11-22 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551763 A Genome-Wide Association Study Reveals a BDNF-Centered Molecular Network Associated with Alcohol Dependence and Related Clinical Measures. Amount of alcohol consumed in alcohol dependence (dominant genetic model) 192 Russian ancestry individuals NA Illumina [381084] 1 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90245790 Genome-wide genotyping array 2023-01-30 36505257 Wu Q 2022-11-24 Front Nutr www.ncbi.nlm.nih.gov/pubmed/36505257 Gamma-glutamyl-leucine levels are causally associated with elevated cardio-metabolic risks. Gamma-glutamylleucine levels 1,062 East Asian ancestry individuals 227 East Asian ancestry individuals Illumina [40001312] (imputed) 4 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90245764 Genome-wide genotyping array 2023-02-01 36496446 Seviiri M 2022-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36496446 A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma. Basal cell carcinoma (MTAG) 20,791 European ancestry cases, 286,893 European ancestry controls 251,963 European ancestry cases, 2,271,667 European ancestry controls Affymetrix, Illumina [5301239] (imputed) 72 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90137411 Genome-wide genotyping array 2023-02-01 36496446 Seviiri M 2022-12-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36496446 A multi-phenotype analysis reveals 19 susceptibility loci for basal cell carcinoma and 15 for squamous cell carcinoma. Squamous cell carcinoma (MTAG) 7,402 European ancestry cases, 286,892 European ancestry controls 134,700 European ancestry cases, 2,394,699 European ancestry controls Affymetrix, Illumina [5301239] (imputed) 28 squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707 GCST90137412 Genome-wide genotyping array 2023-02-01 35587468 Hodgson S 2022-05-19 PLoS Med www.ncbi.nlm.nih.gov/pubmed/35587468 Integrating polygenic risk scores in the prediction of type 2 diabetes risk and subtypes in British Pakistanis and Bangladeshis: A population-based cohort study. Type 2 diabetes 12,875 Bangladeshis, Pakistanis ancestry individuals NA Illumina [NR] (imputed) 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90245849 Genome-wide genotyping array 2023-02-14 36268685 Udagawa C 2022-10-21 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/36268685 Association between genetic variants and the risk of nivolumab-induced immune-related adverse events. Nivolumab-induced immune-related adverse events in cancer 315 Japanese ancestry cases, 86 Japanese ancestry controls 205 Japanese ancestry cases, 16 Japanese ancestry controls Illumina [364954] 4 immune system toxicity, response to nivolumab http://www.ebi.ac.uk/efo/EFO_0011053, http://www.ebi.ac.uk/efo/EFO_0803366 GCST90244681 Genome-wide genotyping array 2023-02-14 36268685 Udagawa C 2022-10-21 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/36268685 Association between genetic variants and the risk of nivolumab-induced immune-related adverse events. Nivolumab-induced hypothyroidism in cancer 24 Japanese ancestry cases, 377 Japanese ancestry controls 18 Japanese ancestry cases, 203 Japanese ancestry controls Illumina [364954] 1 hypothyroidism, response to nivolumab http://www.ebi.ac.uk/efo/EFO_0004705, http://www.ebi.ac.uk/efo/EFO_0803366 GCST90244682 Genome-wide genotyping array 2023-01-17 36269708 Selvaraj MS 2022-10-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/36269708 Genome-wide discovery for diabetes-dependent triglycerides-associated loci. Triglyceride levels in type 2 diabetes 21,176 European ancestry individuals NA Affymetrix [NR] (imputed) 19 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90244679 Genome-wide genotyping array 2023-01-17 36269708 Selvaraj MS 2022-10-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/36269708 Genome-wide discovery for diabetes-dependent triglycerides-associated loci. Triglyceride levels in non-type 2 diabetes 402,944 European ancestry individuals NA Affymetrix [NR] (imputed) 315 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90244680 Genome-wide genotyping array 2023-01-19 36382269 Hayashi S 2022-10-29 Rheumatol Adv Pract www.ncbi.nlm.nih.gov/pubmed/36382269 A genome-wide association study identifying single nucleotide polymorphisms in the PPFIBP2 gene was predictive for interstitial lung disease in rheumatoid arthritis patients. Interstitial lung diseases in rheumatoid arthritis 57 Japanese ancestry cases, 249 Japanese ancestry controls NA Illumina [278347] 6 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90244699 Genome-wide genotyping array 2022-08-05 35835914 Watanabe K 2022-07-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35835914 Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways. Insomnia 593,724 European ancestry cases, 1,771,286 European ancestry controls NA Illumina [10713943] (imputed) 2214 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90131901 Genome-wide genotyping array 2022-08-05 35835914 Watanabe K 2022-07-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35835914 Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways. Insomnia 222,753 European ancestry male cases, 993,280 European ancestry male controls NA Illumina [10177566] (imputed) 232 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90131902 Genome-wide genotyping array 2022-08-05 35835914 Watanabe K 2022-07-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35835914 Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways. Insomnia 390,751 European ancestry female cases, 1,018,386 European ancestry female controls NA Illumina [10288913] (imputed) 952 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90131903 Genome-wide genotyping array 2023-02-16 36584111 Ahmed WU 2022-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/36584111 Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Inguinal hernia 18,791 European ancestry cases, 93,955 European ancestry controls NA Affymetrix [8397536] (imputed) 28 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90245889 Genome-wide genotyping array 2023-02-16 36584111 Ahmed WU 2022-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/36584111 Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Femoral hernia 973 European ancestry cases, 4,865 European ancestry controls NA Affymetrix [8397536] (imputed) 1 femoral hernia http://www.ebi.ac.uk/efo/EFO_1001791 GCST90245890 Genome-wide genotyping array 2023-02-16 36584111 Ahmed WU 2022-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/36584111 Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Umbilical hernia 5,356 European ancestry cases, 26,780 European ancestry controls NA Affymetrix [8397536] (imputed) 5 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90245891 Genome-wide genotyping array 2023-02-16 36584111 Ahmed WU 2022-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/36584111 Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Hiatus hernia 32,298 European ancestry cases, 161,490 European ancestry controls NA Affymetrix [8397536] (imputed) 8 Hiatus hernia http://purl.obolibrary.org/obo/HP_0002036 GCST90245892 Genome-wide genotyping array 2023-02-16 36584111 Ahmed WU 2022-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/36584111 Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Hernia (two or more subtypes) 5,219 European ancestry cases, 26,095 European ancestry controls NA Affymetrix [8397536] (imputed) 6 Hernia http://purl.obolibrary.org/obo/HP_0100790 GCST90245893 Genome-wide genotyping array 2023-02-16 36584111 Ahmed WU 2022-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/36584111 Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Hernia (any subtypes) 62,637 European ancestry cases, 313,185 European ancestry controls NA Affymetrix [8397536] (imputed) 25 Hernia http://purl.obolibrary.org/obo/HP_0100790 GCST90245894 Genome-wide genotyping array 2023-02-16 36584111 Ahmed WU 2022-12-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/36584111 Shared genetic architecture of hernias: A genome-wide association study with multivariable meta-analysis of multiple hernia phenotypes. Hernia 57,418 European ancestry cases, 287,090 European ancestry controls NA Affymetrix [8896286] (imputed) 24 Hernia http://purl.obolibrary.org/obo/HP_0100790 GCST90245895 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-acetamidobutanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90102819 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-allylcatechol sulfate (X-12212) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90102820 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-allylphenol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90102821 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-androsten-3alpha,17alpha-diol monosulfate (2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 4-androsten-3alpha,17alpha-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0022089 GCST90102822 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-androsten-3alpha,17alpha-diol monosulfate (3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 4-androsten-3alpha,17alpha-diol monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0022090 GCST90102823 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-androsten-3beta,17beta-diol disulfate (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 4-androsten-3beta,17beta-diol disulfate 1 measurement http://www.ebi.ac.uk/efo/EFO_0021113 GCST90102824 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-androsten-3beta,17beta-diol disulfate (2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 4-androsten-3beta,17beta-diol disulfate 2 measurement http://www.ebi.ac.uk/efo/EFO_0021114 GCST90102825 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-androsten-3beta,17beta-diol monosulfate (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 4-androsten-3beta,17beta-diol disulfate 1 measurement http://www.ebi.ac.uk/efo/EFO_0021113 GCST90102826 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-androsten-3beta,17beta-diol monosulfate (2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 4-androsten-3beta,17beta-diol disulfate 2 measurement http://www.ebi.ac.uk/efo/EFO_0021114 GCST90102827 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-ethylcatechol sulfate (X-12230) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90102828 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-ethylphenylsulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90102829 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-guanidinobutanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90102830 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-hydroxy-2-oxoglutaric acid levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90102831 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-hydroxychlorothalonil levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 4-hydroxychlorothalonil measurement http://www.ebi.ac.uk/efo/EFO_0800992 GCST90102832 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-hydroxyhippurate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90102833 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-hydroxyphenylpyruvate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90102834 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-methyl-2-oxopentanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90102835 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-methylcatechol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90102836 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 4-vinylphenol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90102837 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5,6-dihydrothymine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90102838 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5,6-dihydrouridine (X-11429) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 5,6-dihydrouridine measurement http://www.ebi.ac.uk/efo/EFO_0800631 GCST90102839 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-acetylamino-6-amino-3-methyluracil levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90102840 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-acetylamino-6-formylamino-3-methyluracil levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 10 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90102841 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800288 GCST90102842 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5alpha-androstan-3beta,17alpha-diol disulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90102843 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800403 GCST90102744 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800184 GCST90102745 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-dihomo-linolenoyl-GPC (18:0/20:3n3 or 6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-stearoyl-2-dihomo-linolenoyl-GPC (18:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800434 GCST90102746 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-dihomo-linolenoyl-GPI (18:0/20:3n3 or 6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 8 1-stearoyl-2-dihomo-linolenoyl-GPI (18:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0022085 GCST90102747 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-docosahexaenoyl-gpc (18:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800392 GCST90102748 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800411 GCST90102749 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800455 GCST90102750 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800456 GCST90102751 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-linoleoyl-gpc (18:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90102752 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800402 GCST90102753 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800413 GCST90102754 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-oleoyl-gpc (18:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-2-oleoyl-GPC (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800389 GCST90102755 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-oleoyl-GPE (18:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-2-oleoyl-GPE (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800269 GCST90102756 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-gpc (18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-stearoyl-GPC (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800217 GCST90102757 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-GPE (18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800227 GCST90102758 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-GPI (18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800188 GCST90102759 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearyl-GPC (O-18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-stearyl-GPC (O-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800460 GCST90102760 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) (X-11564) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90102761 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2,3-dihydroxyisovalerate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90102762 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2,6-dihydroxybenzoic acid (X-09789) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90102763 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 21-hydroxypregnenolone disulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90102764 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-aminoadipate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0800137 GCST90102765 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-aminobutyrate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90102766 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-aminoheptanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90102767 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-aminooctanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90102768 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-eicosapentaenoyl-GPC (16:0/20:5) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmitoyl-2-eicosapentaenoyl-GPC (16:0/20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800408 GCST90102719 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-eicosapentaenoyl-GPE (16:0/20:5) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-palmitoyl-2-eicosapentaenoyl-GPE (16:0/20:5) measurement http://www.ebi.ac.uk/efo/EFO_0022083 GCST90102720 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-linoleoyl-gpc (16:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90102721 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800272 GCST90102722 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800609 GCST90102723 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-oleoyl-gpc (16:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90102724 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 7 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800608 GCST90102725 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800439 GCST90102726 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-palmitoyl-2-palmitoleoyl-GPC (16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0022084 GCST90102727 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90102728 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-GPC (16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800214 GCST90102729 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-GPE (16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800245 GCST90102730 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-GPI (16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-palmitoyl-GPI (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800257 GCST90102731 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmityl-2-arachidonoyl-GPC (o-16:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmityl-2-arachidonoyl-GPC (O-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800426 GCST90102732 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmityl-2-linoleoyl-GPC (O-16:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90102733 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmityl-2-oleoyl-GPC (o-16:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmityl-2-oleoyl-GPC (O-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800425 GCST90102734 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmityl-2-palmitoyl-GPC (O-16:0/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmityl-2-palmitoyl-GPC (O-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800515 GCST90102735 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmityl-2-stearoyl-GPC (O-16:0/18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90102736 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmityl-GPC (o-16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-palmityl-GPC (O-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800183 GCST90102737 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-pentadecanoyl-2-arachidonoyl-GPC (15:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-pentadecanoyl-2-arachidonoyl-GPC (15:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800446 GCST90102738 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-pentadecanoyl-2-docosahexaenoyl-GPC (15:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-pentadecanoyl-2-docosahexaenoyl-GPC (15:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800447 GCST90102739 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-pentadecanoyl-GPC (15:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-pentadecanoyl-GPC (15:0) measurement http://www.ebi.ac.uk/efo/EFO_0800307 GCST90102740 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-ribosyl-imidazoleacetate (X-11334) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 7 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90102741 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-adrenoyl-GPC (18:0/22:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-2-adrenoyl-GPC (18:0/22:4) measurement http://www.ebi.ac.uk/efo/EFO_0800459 GCST90102742 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90102743 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) (X-02249) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) measurement http://www.ebi.ac.uk/efo/EFO_0800566 GCST90102794 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90102795 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-formylindole (X-16071) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90102796 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxy-2-ethylpropionate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90102797 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxy-3-methylglutarate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90102798 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxy-5-cholestenoic acid levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-hydroxy-5-cholestenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0022087 GCST90102799 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxybutyrate (bhba) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90102800 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxydecanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800198 GCST90102801 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxyhexanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90102802 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxyhippurate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90102803 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxyisobutyrate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90102804 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxylaurate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-hydroxylaurate measurement http://www.ebi.ac.uk/efo/EFO_0800204 GCST90102805 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxyoctanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800193 GCST90102806 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-hydroxypyridine sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90102807 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-indoxyl sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022088 GCST90102808 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-methoxycatechol sulfate (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90102809 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-methoxytyrosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 8 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90102810 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-methyl catechol sulfate (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90102811 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-methyl-2-oxobutyrate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90102812 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-methyl-2-oxovalerate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90102813 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-methylhistidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90102814 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-methylxanthine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90102815 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-phenylpropionate (hydrocinnamate) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90102816 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-phosphoglycerate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90102817 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-ureidopropionate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90102818 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-aminophenol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90102769 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-arachidonoyl-GPC (20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-arachidonoyl-GPC (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800237 GCST90102770 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-arachidonoyl-GPE (20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 2-arachidonoyl-GPE (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800260 GCST90102771 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-docosahexaenoyl-GPC (22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-docosahexaenoyl-GPC (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800243 GCST90102772 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxy-3-methylvalerate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 2-hydroxy-3-methylvalerate measurement http://www.ebi.ac.uk/efo/EFO_0800027 GCST90102773 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxybutyrate/2-hydroxyisobutyrate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-hydroxybutyrate/2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022086 GCST90102774 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxydecanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800347 GCST90102775 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxyglutarate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90102776 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxyhippurate (salicylurate) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90102777 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxyoctanoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90102778 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxypalmitate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90102779 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-hydroxystearate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90102780 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-linoleoyl-GPC (18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800239 GCST90102781 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-linoleoyl-GPE (18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800264 GCST90102782 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-methylbutyrylcarnitine (C5) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-methylbutyrylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800026 GCST90102783 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-myristoyl-GPC (14:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-myristoyl-GPC (14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800242 GCST90102784 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-oleoyl-GPC (18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800238 GCST90102785 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-oleoyl-GPE (18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800254 GCST90102786 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-oxoarginine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90102787 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-palmitoyl-GPC (16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 2-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800241 GCST90102788 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-palmitoyl-GPE (16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800255 GCST90102789 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 2-stearoyl-GPE (18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 2-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800343 GCST90102790 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-(4-hydroxyphenyl) lactate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90102791 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-amino-2-piperidone (X-24766) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90102792 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 3-aminoisobutyrate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90102793 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N4-acetylcytidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90103069 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N6,n6,n6-trimethyllysine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90103070 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N6-acetyllysine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90103071 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetyl-2-aminooctanoate (X-12511) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90103072 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylalanine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90103073 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylarginine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90103074 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylaspartate (naa) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 N-acetylaspartate (NAA) measurement http://www.ebi.ac.uk/efo/EFO_0800012 GCST90103075 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetyl-beta-alanine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90103076 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylcarnosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022101 GCST90103077 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylglucosamine/n-acetylgalactosamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 N-acetylgalactosamine measurement, N-acetylglucosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149, http://www.ebi.ac.uk/efo/EFO_0801068 GCST90103078 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylglutamate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90103079 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylglutamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90103080 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylglycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90103081 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylhistidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90103082 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetyl-isoputreanine (X-12688) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 13 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90103083 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylleucine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90103084 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylmethionine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90103085 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylneuraminate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90103086 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylphenylalanine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90103087 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylputrescine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90103088 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylserine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90103089 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetyltaurine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90103090 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylthreonine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90103091 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-delta-acetylornithine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90103092 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-formylmethionine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 N-formylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800128 GCST90103093 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Nicotinamide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90103094 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-methylpipecolate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 N-methylpipecolate measurement http://www.ebi.ac.uk/efo/EFO_0800988 GCST90103095 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-methylproline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90103096 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Nonadecanoate (19:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90103097 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-palmitoylglycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 N-palmitoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800342 GCST90103098 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-palmitoyl-sphinganine (d18:0/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90103099 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-palmitoyl-sphingosine (d18:1/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90103100 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-stearoyl-sphingosine (d18:1/18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800613 GCST90103101 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-trimethyl 5-aminovalerate (X-21365) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90103102 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Octadecenedioate (c18:1-dc) (X-11538) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 octadecenedioate (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800563 GCST90103103 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Octanoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90103104 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleate/vaccenate (18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 vaccenate (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800397 GCST90103105 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoyl ethanolamide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 oleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800604 GCST90103106 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoyl-arachidonoyl-glycerol (18:1/20:4) [2] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 7 oleoyl-arachidonoyl-glycerol (18:1/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800508 GCST90103107 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90103108 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoylcholine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 oleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800477 GCST90103109 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoyl-linoleoyl-glycerol (18:1/18:2) [1] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 oleoyl-linoleoyl-glycerol (18:1/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800332 GCST90103110 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoyl-linoleoyl-glycerol (18:1/18:2) [2] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 oleoyl-linoleoyl-glycerol (18:1/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800333 GCST90103111 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoyl-oleoyl-glycerol (18:1/18:1) [1] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 oleoyl-oleoyl-glycerol (18:1/18:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800497 GCST90103112 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oleoyl-oleoyl-glycerol (18:1/18:1) [2] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 oleoyl-oleoyl-glycerol (18:1/18:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800498 GCST90103113 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. O-methylcatechol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 O-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022102 GCST90103114 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ornithine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90103115 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Orotate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90103116 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Orotidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90103117 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. O-sulfo-l-tyrosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-11423--O-sulfo-L-tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021231 GCST90103118 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phosphatidylcholine (14:0/14:0, 16:0/12:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 phosphatidylcholine (14:0/14:0, 16:0/12:0) measurement http://www.ebi.ac.uk/efo/EFO_0800485 GCST90103144 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phosphatidylcholine (15:0/18:1, 17:0/16:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 phosphatidylcholine (15:0/18:1, 17:0/16:1, 16:0/17:1) measurement http://www.ebi.ac.uk/efo/EFO_0800486 GCST90103145 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phosphatidylcholine (16:0/22:5n3, 18:1/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 phosphatidylcholine (16:0/22:5n3, 18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800467 GCST90103146 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phosphatidylcholine (18:0/20:2, 20:0/18:2, 18:1/20:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 phosphatidylcholine (18:0/20:2, 20:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800488 GCST90103147 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phosphoethanolamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90103148 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Picolinoylglycine (X-12170) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90103149 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pipecolate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90103150 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Piperine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90103151 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pregn steroid monosulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Pregn steroid monosulfate measurement http://www.ebi.ac.uk/efo/EFO_0022104 GCST90103152 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pregnanediol-3-glucuronide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90103153 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pregnen-diol disulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90103154 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pregnenetriol disulfate (X-11440) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90103155 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pregnenolone sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 pregnenolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800303 GCST90103156 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pro-hydroxy-pro levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90103157 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Proline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90103158 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Propionylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90103159 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pseudouridine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90103160 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pyridoxate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90103161 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pyroglutamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST90103162 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pyrraline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90103163 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pyruvate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90103164 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Quinate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90103165 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Quinolinate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90103166 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Retinol (Vitamin A) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90103167 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ribitol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90103168 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Malate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90103044 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Maleate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90103045 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Maltose levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Maltose measurement http://www.ebi.ac.uk/efo/EFO_0021649 GCST90103046 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Mannitol/sorbitol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 mannitol measurement, sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0021027, http://www.ebi.ac.uk/efo/EFO_0010533 GCST90103047 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Mannose levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90103048 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Margarate (17:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90103049 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Metabolonic lactone sulfate (X-12063) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 15 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90103050 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Methionine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90103051 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Methionine sulfone levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90103052 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Methionine sulfoxide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90103053 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Methyl glucopyranoside (alpha + beta) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90103054 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Methyl indole-3-acetate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 methyl indole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0801063 GCST90103055 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Methyl-4-hydroxybenzoate sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90103056 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Methylsuccinate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90103057 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Myo-inositol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90103058 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Myristate (14:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90103059 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Myristoleate (14:1n5) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90103060 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Myristoleoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90103061 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Myristoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90103062 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-(2-furoyl)glycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 N-(2-furoyl)glycine measurement http://www.ebi.ac.uk/efo/EFO_0800947 GCST90103063 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N,n-dimethylalanine (X-23585) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90103064 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N1-methyl-2-pyridone-5-carboxamide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90103065 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N1-methyladenosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90103066 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N1-methylinosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90103067 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N2,n2-dimethylguanosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90103068 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Oxalate (ethanedioate) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90103119 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitate (16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90103120 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoleate (16:1n7) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90103121 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoleoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 palmitoleoylcarnitine (C16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800493 GCST90103122 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoleoyl-linoleoyl-glycerol (16:1/18:2) [1] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 palmitoleoyl-linoleoyl-glycerol (16:1/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800504 GCST90103123 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 palmitoyl dihydrosphingomyelin (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800400 GCST90103124 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoyl sphingomyelin (d18:1/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90103125 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoyl-arachidonoyl-glycerol (16:0/20:4) [2] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 Palmitoyl-arachidonoyl-glycerol (16:0/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0022103 GCST90103126 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90103127 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoylcholine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 palmitoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800473 GCST90103128 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoyl-linoleoyl-glycerol (16:0/18:2) [1] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 palmitoyl-linoleoyl-glycerol (16:0/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800438 GCST90103129 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoyl-linoleoyl-glycerol (16:0/18:2) [2] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 palmitoyl-linoleoyl-glycerol (16:0/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800438 GCST90103130 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoyl-oleoyl-glycerol (16:0/18:1) [2] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 palmitoyl-oleoyl-glycerol (16:0/18:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800496 GCST90103131 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) (X-24106) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800591 GCST90103132 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Pantothenate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90103133 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Paraxanthine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90103134 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. P-cresol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90103135 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. P-cresol-glucuronide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90103136 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phenol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90103137 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phenylacetylglutamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90103138 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phenylalanine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90103139 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phenylalanyltryptophan levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 phenylalanyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800679 GCST90103140 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phenyllactate (pla) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90103141 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phenylpyruvate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 phenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800132 GCST90103142 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Phosphate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90103143 Genome-wide genotyping array 2023-01-10 36301540 Deak JD 2022-10-03 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/36301540 Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder. Maximum habitual alcohol consumption 29,132 African ancestry individuals, 218,623 European ancestry individuals NA Affymetrix [NR] (imputed) 14 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90244185 Genome-wide genotyping array 2023-01-10 36301540 Deak JD 2022-10-03 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/36301540 Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder. Maximum habitual alcohol consumption 218,623 European ancestry individuals NA Affymetrix [NR] (imputed) 10 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90244186 Genome-wide genotyping array 2023-01-10 36301540 Deak JD 2022-10-03 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/36301540 Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder. Maximum habitual alcohol consumption 29,132 African ancestry individuals NA Affymetrix [NR] (imputed) 2 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90244187 Genome-wide genotyping array 2023-01-10 36301540 Deak JD 2022-10-03 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/36301540 Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder. Maximum habitual alcohol consumption (MTAG) 353,981 European ancestry individuals NA Affymetrix [NR] (imputed) 31 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90244188 Genome-wide genotyping array 2023-01-10 36301540 Deak JD 2022-10-03 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/36301540 Genome-Wide Investigation of Maximum Habitual Alcohol Intake in US Veterans in Relation to Alcohol Consumption Traits and Alcohol Use Disorder. Problematic alcohol use (MTAG) 422,491 European ancestry individuals NA Affymetrix [NR] (imputed) 42 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90244189 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPC (p-18:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPC (P-18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800424 GCST90102645 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPE (p-18:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPE (P-18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800418 GCST90102646 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-linoleoyl-GPC (p-18:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-stearoyl)-2-linoleoyl-GPC (P-18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800451 GCST90102647 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (p-18:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90102648 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-oleoyl-GPC (p-18:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-stearoyl)-2-oleoyl-GPC (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800393 GCST90102649 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-oleoyl-GPE (p-18:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800395 GCST90102650 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-GPC (P-18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-stearoyl)-GPC (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800325 GCST90102651 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-GPE (p-18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-stearoyl)-GPE (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800335 GCST90102652 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,2,3-benzenetriol sulfate (2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90102653 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,2-dilinoleoyl-GPC (18:2/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1,2-dilinoleoyl-GPC (18:2/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800388 GCST90102654 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,2-dipalmitoyl-gpc (16:0/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1,2-dipalmitoyl-GPC (16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800189 GCST90102655 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,3,7-trimethylurate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90102656 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,3-dimethylurate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90102657 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,5-anhydroglucitol (1,5-ag) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90102658 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,7-dimethylurate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90102659 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 10-heptadecenoate (17:1n7) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 10-heptadecenoate 17:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021060 GCST90102660 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 10-nonadecenoate (19:1n9) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90102661 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 10-undecenoate (11:1n1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90102662 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 11beta-hydroxyandrosterone glucuronide (X-12846) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90102663 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 12,13-DiHOME levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90102664 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 13-HODE + 9-HODE levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 13-HODE + 9-HODE measurement http://www.ebi.ac.uk/efo/EFO_0800308 GCST90102665 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 15-methylpalmitate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 15-methylpalmitate measurement http://www.ebi.ac.uk/efo/EFO_0022076 GCST90102666 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 16a-hydroxy DHEA 3-sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90102667 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 16-hydroxypalmitate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 16-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0022077 GCST90102668 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 17-methylstearate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 17-methylstearate measurement http://www.ebi.ac.uk/efo/EFO_0022078 GCST90102669 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-adrenoyl-GPC (22:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-adrenoyl-GPC (22:4) measurement http://www.ebi.ac.uk/efo/EFO_0800321 GCST90102670 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-arachidonoyl-gpc (20:4n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-arachidonoyl-GPC (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800234 GCST90102671 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-arachidonoyl-GPE (20:4n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-arachidonoyl-GPE (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800248 GCST90102672 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-arachidonoyl-GPI (20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-arachidonoyl-GPI (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800256 GCST90102673 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-arachidoyl-2-arachidonoyl-GPC (20:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-arachidoyl-2-arachidonoyl-GPC (20:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0022079 GCST90102674 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-arachidoyl-GPC (20:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-arachidoyl-GPC (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800222 GCST90102675 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-carboxyethylphenylalanine (X-15497) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-carboxyethylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800101 GCST90102676 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-dihomo-linolenoyl-GPC (20:3n3 or 6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-dihomo-linolenoyl-GPC (20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800235 GCST90102677 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-dihomo-linolenoyl-GPE (20:3n3 or 6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-dihomo-linolenoyl-GPE (20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800358 GCST90102678 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-dihomo-linoleoyl-GPC (20:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-dihomo-linoleoyl-GPC (20:2) measurement http://www.ebi.ac.uk/efo/EFO_0800236 GCST90102679 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-docosahexaenoyl-GPC (22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-docosahexaenoyl-GPC (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800244 GCST90102680 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-docosahexaenoyl-GPE (22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-docosahexaenoyl-GPE (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800296 GCST90102681 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-docosapentaenoyl-GPC (22:5n3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-docosapentaenoyl-GPC (22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800298 GCST90102682 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-eicosapentaenoyl-GPC (20:5) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-eicosapentaenoyl-GPC (20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800355 GCST90102683 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-eicosapentaenoyl-GPE (20:5) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-eicosapentaenoyl-GPE (20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800353 GCST90102684 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-eicosenoyl-GPC (20:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-eicosenoyl-GPC (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800356 GCST90102685 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-lignoceroyl-GPC (24:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-lignoceroyl-GPC (24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800322 GCST90102686 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-linolenoyl-GPC (18:3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-linolenoyl-GPC (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800354 GCST90102687 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-linoleoyl-2-docosahexaenoyl-GPC (18:2/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-linoleoyl-2-docosahexaenoyl-GPC (18:2/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0022080 GCST90102688 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800483 GCST90102689 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-linoleoylglycerol (18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800199 GCST90102690 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-linoleoyl-gpc (18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800223 GCST90102691 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-linoleoyl-GPE (18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800247 GCST90102692 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-linoleoyl-GPI (18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-linoleoyl-GPI (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800266 GCST90102693 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-margaroyl-2-arachidonoyl-GPC (17:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-margaroyl-2-arachidonoyl-GPC (17:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0022081 GCST90102694 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24849 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-24849 measurement http://www.ebi.ac.uk/efo/EFO_0800909 GCST90103344 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24870 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 X-24870 measurement http://www.ebi.ac.uk/efo/EFO_0022143 GCST90103345 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Xanthine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90103346 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Xanthurenate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90103347 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1,5-anhydroglucitol (1,5-ag) levels 10,577 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90239711 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. N-acetylglycine levels 10,577 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90239712 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. (S)-a-amino-omega-caprolactam (X-13737) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 (S)-a-amino-omega-caprolactam (X-13737) measurement http://www.ebi.ac.uk/efo/EFO_0022073 GCST90102626 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-oleoyl)-2-docosahexaenoyl-GPE (p-18:1/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-oleoyl)-2-docosahexaenoyl-GPE (P-18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800490 GCST90102627 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-oleoyl)-GPC (p-18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-oleoyl)-GPC (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800324 GCST90102628 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-oleoyl)-GPE (p-18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-oleoyl)-GPE (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800359 GCST90102629 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90102630 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (p-16:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800417 GCST90102631 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPC (p-16:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPC (P-16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800421 GCST90102632 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPE (p-16:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPE (P-16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800416 GCST90102633 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (p-16:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800422 GCST90102634 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (p-16:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800440 GCST90102635 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-myristoyl-GPC (p-16:0/14:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-(1-enyl-palmitoyl)-2-myristoyl-GPC (P-16:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800465 GCST90102636 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-oleoyl-gpc (p-16:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800420 GCST90102637 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (p-16:0/18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800419 GCST90102638 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800464 GCST90102639 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800466 GCST90102640 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-GPC (p-16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-palmitoyl)-GPC (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800323 GCST90102641 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-palmitoyl)-GPE (p-16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-(1-enyl-palmitoyl)-GPE (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800334 GCST90102642 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPC (p-18:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-(1-enyl-stearoyl)-2-arachidonoyl-GPC (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800394 GCST90102643 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (p-18:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800415 GCST90102644 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-margaroyl-2-docosahexaenoyl-GPC (17:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-margaroyl-2-docosahexaenoyl-GPC (17:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800448 GCST90102695 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-margaroyl-GPC (17:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-margaroyl-GPC (17:0) measurement http://www.ebi.ac.uk/efo/EFO_0800215 GCST90102696 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-methyl-5-imidazoleacetate (X-14838) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90102697 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-methylhistidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90102698 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-methylimidazoleacetate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-methylimidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0022082 GCST90102699 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-methylnicotinamide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90102700 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-methylxanthine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90102701 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800453 GCST90102702 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-myristoyl-2-docosahexaenoyl-GPC (14:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-myristoyl-2-docosahexaenoyl-GPC (14:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800454 GCST90102703 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-myristoyl-2-linoleoyl-GPC (14:0/18:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-myristoyl-2-linoleoyl-GPC (14:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800452 GCST90102704 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-myristoyl-2-palmitoyl-gpc (14:0/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800191 GCST90102705 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-myristoyl-GPC (14:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-myristoyl-GPC (14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800221 GCST90102706 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-nonadecanoyl-GPC (19:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-nonadecanoyl-GPC (19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800357 GCST90102707 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800449 GCST90102708 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-oleoyl-GPC (18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800218 GCST90102709 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-oleoyl-GPE (18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800246 GCST90102710 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-oleoyl-GPI (18:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-oleoyl-GPI (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800265 GCST90102711 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoleoyl-GPC (16:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800231 GCST90102712 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoleoyl-GPE (16:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 1-palmitoleoyl-GPE (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800267 GCST90102713 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800390 GCST90102714 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800409 GCST90102715 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800412 GCST90102716 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-docosahexaenoyl-gpc (16:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800391 GCST90102717 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800410 GCST90102718 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-14056 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90103269 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-14568 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-14568 measurement http://www.ebi.ac.uk/efo/EFO_0022119 GCST90103270 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-14939 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-14939 measurement http://www.ebi.ac.uk/efo/EFO_0800747 GCST90103271 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-15469 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-15469 measurement http://www.ebi.ac.uk/efo/EFO_0800750 GCST90103272 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-15486 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90103273 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-15492 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-15492 measurement http://www.ebi.ac.uk/efo/EFO_0800752 GCST90103274 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-15666 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-15666 measurement http://www.ebi.ac.uk/efo/EFO_0800754 GCST90103275 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-16580 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90103276 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-16935 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-16935 measurement http://www.ebi.ac.uk/efo/EFO_0800763 GCST90103277 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-16938 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-16938 measurement http://www.ebi.ac.uk/efo/EFO_0800764 GCST90103278 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-16944 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-16944 measurement http://www.ebi.ac.uk/efo/EFO_0800765 GCST90103279 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-16946 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-16946 measurement http://www.ebi.ac.uk/efo/EFO_0800766 GCST90103280 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-16964 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-16964 measurement http://www.ebi.ac.uk/efo/EFO_0020011 GCST90103281 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-17185 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-17185 measurement http://www.ebi.ac.uk/efo/EFO_0800770 GCST90103282 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-17325 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-17325 measurement http://www.ebi.ac.uk/efo/EFO_0800771 GCST90103283 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-17335 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90103284 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-17653 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-17653 measurement http://www.ebi.ac.uk/efo/EFO_0800783 GCST90103285 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-17654 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 12 X-17654 measurement http://www.ebi.ac.uk/efo/EFO_0800784 GCST90103286 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-17676 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90103287 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-17690 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-17690 measurement http://www.ebi.ac.uk/efo/EFO_0800788 GCST90103288 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-18899 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-18899 measurement http://www.ebi.ac.uk/efo/EFO_0800793 GCST90103289 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-18913 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-18913 measurement http://www.ebi.ac.uk/efo/EFO_0800795 GCST90103290 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-18921 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 X-18921 measurement http://www.ebi.ac.uk/efo/EFO_0800796 GCST90103291 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-19141 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 X-19141 measurement http://www.ebi.ac.uk/efo/EFO_0800799 GCST90103292 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-19438 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-19438 measurement http://www.ebi.ac.uk/efo/EFO_0800801 GCST90103293 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23756 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 X-23756 measurement http://www.ebi.ac.uk/efo/EFO_0022126 GCST90103319 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23765 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-23765 measurement http://www.ebi.ac.uk/efo/EFO_0022127 GCST90103320 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23782 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-23782 measurement http://www.ebi.ac.uk/efo/EFO_0800865 GCST90103321 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23997 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90103322 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24020 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 7 X-24020 measurement http://www.ebi.ac.uk/efo/EFO_0022128 GCST90103323 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24027 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24027 measurement http://www.ebi.ac.uk/efo/EFO_0022129 GCST90103324 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24243 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-24243 measurement http://www.ebi.ac.uk/efo/EFO_0022130 GCST90103325 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24295 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24295 measurement http://www.ebi.ac.uk/efo/EFO_0800869 GCST90103326 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24306 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24306 measurement http://www.ebi.ac.uk/efo/EFO_0800870 GCST90103327 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24307 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-24307 measurement http://www.ebi.ac.uk/efo/EFO_0800871 GCST90103328 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24309 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 14 X-24309 measurement http://www.ebi.ac.uk/efo/EFO_0800872 GCST90103329 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24431 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-24431 measurement http://www.ebi.ac.uk/efo/EFO_0800882 GCST90103330 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24452 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24452 measurement http://www.ebi.ac.uk/efo/EFO_0022131 GCST90103331 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24512 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-24512 measurement http://www.ebi.ac.uk/efo/EFO_0022132 GCST90103332 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24513 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-24513 measurement http://www.ebi.ac.uk/efo/EFO_0022133 GCST90103333 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24699 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-24699 measurement http://www.ebi.ac.uk/efo/EFO_0800902 GCST90103334 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24738 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24738 measurement http://www.ebi.ac.uk/efo/EFO_0022134 GCST90103335 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24747 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 X-24747 measurement http://www.ebi.ac.uk/efo/EFO_0022135 GCST90103336 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24748 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 10 X-24748 measurement http://www.ebi.ac.uk/efo/EFO_0022136 GCST90103337 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24765 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24765 measurement http://www.ebi.ac.uk/efo/EFO_0022137 GCST90103338 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24803 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24803 measurement http://www.ebi.ac.uk/efo/EFO_0022138 GCST90103339 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24804 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24804 measurement http://www.ebi.ac.uk/efo/EFO_0022139 GCST90103340 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24806 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24806 measurement http://www.ebi.ac.uk/efo/EFO_0022140 GCST90103341 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24813 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24813 measurement http://www.ebi.ac.uk/efo/EFO_0022141 GCST90103342 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-24831 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-24831 measurement http://www.ebi.ac.uk/efo/EFO_0022142 GCST90103343 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 5 temporal synchrony (Fronto-parietal) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245948 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 6 temporal synchrony (Fronto-parietal) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245949 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 7 temporal synchrony (Limbic default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245950 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 8 temporal synchrony (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245951 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 9 temporal synchrony (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245952 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 10 temporal synchrony (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245953 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 11 temporal synchrony (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245954 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 12 temporal synchrony (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245955 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 13 temporal synchrony (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245956 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 14 temporal synchrony (Salience) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245957 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 15 temporal synchrony (Cerebellum) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245958 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 16 temporal synchrony (Executive control) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245959 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 17 temporal synchrony (Auditory) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245960 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 18 temporal synchrony (Subcortical) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245961 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 19 temporal synchrony (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245962 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 20 temporal synchrony (Precuneal default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245963 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 21 temporal synchrony (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245964 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 1 amplitude (blood oxygenation level dependent) (Default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245965 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 2 amplitude (blood oxygenation level dependent) (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245966 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 3 amplitude (blood oxygenation level dependent) (Attention) 22,172 British ancestry individuals NA NR [20381043] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245967 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 4 amplitude (blood oxygenation level dependent) (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245968 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 5 amplitude (blood oxygenation level dependent) (Fronto-parietal) 22,172 British ancestry individuals NA NR [20381043] (imputed) 5 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245969 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 6 amplitude (blood oxygenation level dependent) (Fronto-parietal) 22,172 British ancestry individuals NA NR [20381043] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245970 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 7 amplitude (blood oxygenation level dependent) (Limbic default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245971 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 8 amplitude (blood oxygenation level dependent) (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245972 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 1 amplitude (Default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245923 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 2 amplitude (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245924 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 3 amplitude (Attention) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245925 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 4 amplitude (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245926 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 5 amplitude (Fronto-parietal) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245927 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 6 amplitude (Fronto-parietal) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245928 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 7 amplitude (Limbic default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245929 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 8 amplitude (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245930 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 9 amplitude (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245931 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 10 amplitude (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245932 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 11 amplitude (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245933 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 12 amplitude (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245934 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 13 amplitude (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245935 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 14 amplitude (Salience) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245936 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 15 amplitude (Cerebellum) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245937 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 16 amplitude (Executive control) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245938 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 17 amplitude (Auditory) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245939 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 18 amplitude (Subcortical) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245940 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 19 amplitude (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245941 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 20 amplitude (Precuneal default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245942 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 21 amplitude (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245943 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 1 temporal synchrony (Default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245944 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 2 temporal synchrony (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245945 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 3 temporal synchrony (Attention) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245946 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 4 temporal synchrony (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245947 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 9 amplitude (blood oxygenation level dependent) (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 6 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245973 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 10 amplitude (blood oxygenation level dependent) (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245974 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 11 amplitude (blood oxygenation level dependent) (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245975 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 12 amplitude (blood oxygenation level dependent) (Motor) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245976 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 13 amplitude (blood oxygenation level dependent) (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245977 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 14 amplitude (blood oxygenation level dependent) (Salience) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245978 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 15 amplitude (blood oxygenation level dependent) (Cerebellum) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245979 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 16 amplitude (blood oxygenation level dependent) (Executive control) 22,172 British ancestry individuals NA NR [20381043] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245980 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 17 amplitude (blood oxygenation level dependent) (Auditory) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245981 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 18 amplitude (blood oxygenation level dependent) (Subcortical) 22,172 British ancestry individuals NA NR [20381043] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245982 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 19 amplitude (blood oxygenation level dependent) (Visual) 22,172 British ancestry individuals NA NR [20381043] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245983 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 20 amplitude (blood oxygenation level dependent) (Precuneal default mode network) 22,172 British ancestry individuals NA NR [20381043] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245984 Genome-wide genotyping array 2023-02-09 36462729 Lee S 2022-11-30 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36462729 Amplitudes of resting-state functional networks - investigation into their correlates and biophysical properties. Resting-state network 21 amplitude (blood oxygenation level dependent) (Language) 22,172 British ancestry individuals NA NR [20381043] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90245985 Genome-wide genotyping array 2022-12-02 34989438 Zhu X 2022-01-06 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34989438 Genome-wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores. Blood pressure (pleiotropy model 1 DBP adjusted for estimated causal effects x SBP) 757,601 European ancestry individuals, 318,891 European ancestry, African American or Afro-Caribbean, Native American ancestry, Asian ancestry individuals NA NR [7100000] (imputed) 457 diastolic blood pressure, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90239828 Genome-wide genotyping array 2022-12-02 34989438 Zhu X 2022-01-06 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34989438 Genome-wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores. Blood pressure (pleiotropy model 2 SBP adjusted for estimated causal effects x DBP) 757,601 European ancestry individuals, 318,891 European ancestry, African American or Afro-Caribbean, Native American ancestry, Asian ancestry individuals NA NR [7100000] (imputed) 430 diastolic blood pressure, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90239829 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x menopausal hormone therapy interaction 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 6 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90243993 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x menopausal hormone therapy interaction (2df test) 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 7 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90243994 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x menopausal hormone therapy interaction (3df test) 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 10 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90243995 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x estrogen hormone therapy interaction 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 7 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90243996 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x estrogen hormone therapy interaction (2df test) 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 7 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90243997 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x estrogen hormone therapy interaction (3df test) 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 2 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90243998 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x estrogen-progesterone hormone therapy interaction 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 20 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90243999 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x estrogen-progesterone hormone therapy interaction (2df test) 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 18 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90244000 Genome-wide genotyping array 2022-12-16 35512400 Tian Y 2022-05-05 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/35512400 Genome-Wide Interaction Analysis of Genetic Variants with Menopausal Hormone Therapy for Colorectal Cancer Risk. Colorectal cancer x estrogen-progesterone hormone therapy interaction (3df test) 11,519 European ancestry cases, 16,967 European ancestry controls NA NR [NR] (imputed) 13 colorectal cancer, hormone replacement therapy http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90244001 Genome-wide genotyping array 2023-01-12 35712048 Pain O 2022-04-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/35712048 Identifying the Common Genetic Basis of Antidepressant Response. Remission after antidepressant treatment in major depressive disorder 1,852 European ancestry cases, 3,299 European ancestry controls NA Affymetrix, Illumina [8681460] (imputed) 18 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST90244577 Genome-wide genotyping array 2023-01-12 35712048 Pain O 2022-04-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/35712048 Identifying the Common Genetic Basis of Antidepressant Response. Response to antidepressants (symptom improvement) in major depressive disorder 5,218 European ancestry individuals NA Affymetrix, Illumina [8697190] (imputed) 18 depressive symptom measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007006, http://purl.obolibrary.org/obo/GO_0036276 GCST90244578 Genome-wide genotyping array 2023-01-12 35712048 Pain O 2022-04-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/35712048 Identifying the Common Genetic Basis of Antidepressant Response. Remission after antidepressant treatment in major depressive disorder 226 East Asian ancestry cases, 301 East Asian ancestry controls NA Illumina [7450323] (imputed) 0 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST90244579 Genome-wide genotyping array 2023-01-12 35712048 Pain O 2022-04-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/35712048 Identifying the Common Genetic Basis of Antidepressant Response. Response to antidepressants (symptom improvement) in major depressive disorder 527 East Asian ancestry individuals NA Illumina [7621135] (imputed) 0 depressive symptom measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007006, http://purl.obolibrary.org/obo/GO_0036276 GCST90244580 Genome-wide genotyping array 2022-11-25 34654805 Georges A 2021-10-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34654805 Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases. Fibromuscular dysplasia 1,556 European ancestry cases, 7,100 European ancestry controls NA Illumina [5483710] (imputed) 32 fibromuscular dysplasia http://www.ebi.ac.uk/efo/EFO_1000938 GCST90026612 Genome-wide genotyping array 2023-01-20 36335405 Hernandez-Beeftink T 2022-11-05 Crit Care www.ncbi.nlm.nih.gov/pubmed/36335405 A genome-wide association study of survival in patients with sepsis. Survival in sepsis 506 European ancestry survivors, 181 European ancestry non-survivors 712 European ancestry survivors, 650 European ancestry non-survivors, 411 African American survivors, 290 African American non-survivors Affymetrix [7682187] (imputed) 8 survival time, Sepsis http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/HP_0100806 GCST90244712 Genome-wide genotyping array 2023-01-20 36323703 Patrick MT 2022-11-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36323703 Shared genetic risk factors and causal association between psoriasis and coronary artery disease. Psoriasis or coronary artery disease 11,024 psoriasis cases, 60,801 coronary artery disease cases, 139,840 controls NA NR [8067837] (imputed) 4 psoriasis, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0000676, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90244705 Genome-wide genotyping array 2023-01-26 36419087 Lee G 2022-11-23 Lipids Health Dis www.ncbi.nlm.nih.gov/pubmed/36419087 Sex-related differences in single nucleotide polymorphisms associated with dyslipidemia in a Korean population. Dyslipidemia 15,054 Korean ancestry cases, 37,395 Korean ancestry controls 5,052 Korean ancestry cases, 6,096 Korean ancestry controls Affymetrix [5344653] 3 Rare dyslipidemia http://www.orpha.net/ORDO/Orphanet_101953 GCST90244793 Genome-wide genotyping array 2023-01-26 36419087 Lee G 2022-11-23 Lipids Health Dis www.ncbi.nlm.nih.gov/pubmed/36419087 Sex-related differences in single nucleotide polymorphisms associated with dyslipidemia in a Korean population. Dyslipidemia 5,848 Korean ancestry male cases, 12,402 Korean ancestry male controls 2,407 Korean ancestry male cases, 2,356 Korean ancestry male controls Affymetrix [5344653] 0 Rare dyslipidemia http://www.orpha.net/ORDO/Orphanet_101953 GCST90244794 Genome-wide genotyping array 2023-01-26 36419087 Lee G 2022-11-23 Lipids Health Dis www.ncbi.nlm.nih.gov/pubmed/36419087 Sex-related differences in single nucleotide polymorphisms associated with dyslipidemia in a Korean population. Dyslipidemia 9,206 Korean ancestry female cases, 24,993 Korean ancestry female controls 2,645 Korean ancestry female cases, 3,740 Korean ancestry female controls Affymetrix [5344653] 1 Rare dyslipidemia http://www.orpha.net/ORDO/Orphanet_101953 GCST90244795 Genome-wide genotyping array 2023-01-27 36422279 Lee S 2022-11-19 Metabolites www.ncbi.nlm.nih.gov/pubmed/36422279 Identifying Genetic Variants and Metabolites Associated with Rapid Estimated Glomerular Filtration Rate Decline in Korea Based on Genome-Metabolomic Integrative Analysis. Rapid eGFR decline in diabetes and hypertension 115 Korean ancestry individuals 69 Korean ancestry individuals NR [8000000] (imputed) 1 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90244790 Genome-wide genotyping array 2023-01-17 36271344 Larach DB 2022-10-21 BMC Nephrol www.ncbi.nlm.nih.gov/pubmed/36271344 Limited clinical utility for GWAS or polygenic risk score for postoperative acute kidney injury in non-cardiac surgery in European-ancestry patients. Acute kidney injury (model 1) 1,236 European ancestry cases, 13,010 European ancestry controls NA Illumina [69500000] (imputed) 1 Acute kidney injury http://purl.obolibrary.org/obo/HP_0001919 GCST90244666 Genome-wide genotyping array 2023-01-17 36271344 Larach DB 2022-10-21 BMC Nephrol www.ncbi.nlm.nih.gov/pubmed/36271344 Limited clinical utility for GWAS or polygenic risk score for postoperative acute kidney injury in non-cardiac surgery in European-ancestry patients. Acute kidney injury (model 2) 1,236 European ancestry cases, 13,010 European ancestry controls NA Illumina [69500000] (imputed) 3 Acute kidney injury http://purl.obolibrary.org/obo/HP_0001919 GCST90244667 Genome-wide genotyping array 2023-01-17 36271344 Larach DB 2022-10-21 BMC Nephrol www.ncbi.nlm.nih.gov/pubmed/36271344 Limited clinical utility for GWAS or polygenic risk score for postoperative acute kidney injury in non-cardiac surgery in European-ancestry patients. Acute kidney injury (model 3) 1,236 European ancestry cases, 13,010 European ancestry controls NA Illumina [69500000] (imputed) 3 Acute kidney injury http://purl.obolibrary.org/obo/HP_0001919 GCST90244668 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-measles virus IgG levels 683 European ancestry individuals NA Illumina [NR] (imputed) 4 Anti-measles virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009355 GCST90095158 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-Toxoplasma gondii IgG levels 5,010 European ancestry individuals NA Illumina [NR] (imputed) 4 Anti-Toxoplasma gondii IgG measurement http://www.ebi.ac.uk/efo/EFO_0009353 GCST90095159 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-beta-casein IgG levels 683 European ancestry individuals NA Illumina [NR] (imputed) 2 anti-beta-casein IgG measurement http://www.ebi.ac.uk/efo/EFO_0801087 GCST90095160 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-cytomegalovirus IgG levels 5,010 European ancestry individuals 9,430 European ancestry individuals Illumina [NR] (imputed) 0 Anti-cytomegalovirus IgG measurement http://www.ebi.ac.uk/efo/EFO_0009347 GCST90095161 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-Epstein Barr IgG levels 5,010 European ancestry individuals 9,430 European ancestry individuals Illumina [NR] (imputed) 1 anti-Epstein Barr virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0009273 GCST90095162 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-feline herpes IgG levels 2,764 European ancestry individuals NA Illumina [NR] (imputed) 3 anti-feline herpes IgG measurement http://www.ebi.ac.uk/efo/EFO_0801088 GCST90095163 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-helicobacter pylori IgG levels 4,683 European ancestry individuals 9,430 European ancestry individuals Illumina [NR] (imputed) 0 Anti-Helicobacter pylori IgG measurement http://www.ebi.ac.uk/efo/EFO_0009352 GCST90095164 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-herpes simplex virus 1 IgG levels 683 European ancestry individuals 9,430 European ancestry individuals Illumina [NR] (imputed) 0 Anti-herpes simplex virus 1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0009349 GCST90095165 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-influenza subtype H1N1 IgG levels 683 European ancestry individuals NA Illumina [NR] (imputed) 2 anti-influenza A subtype H1N1 IgG measurement http://www.ebi.ac.uk/efo/EFO_0801089 GCST90095166 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-influenza subtype H3N2 IgG levels 683 European ancestry individuals NA Illumina [NR] (imputed) 2 anti-influenza A subtype H3N2 IgG measurement http://www.ebi.ac.uk/efo/EFO_0801090 GCST90095167 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-saccharomyces cerevisiae IgA levels 357 European ancestry individuals NA Illumina [NR] (imputed) 2 anti-saccharomyces cerevisiae IgA measurement http://www.ebi.ac.uk/efo/EFO_0801091 GCST90095168 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Toxoplasma gondii sag1 antibody levels 1,228 European ancestry individuals 9,430 European ancestry individuals Illumina [NR] (imputed) 0 Anti-Toxoplasma gondii IgG measurement http://www.ebi.ac.uk/efo/EFO_0009353 GCST90095169 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-Theiler's virus IgG levels 683 European ancestry individuals NA Illumina [NR] (imputed) 0 anti-Theiler's virus IgG measurement http://www.ebi.ac.uk/efo/EFO_0801092 GCST90095170 Genome-wide genotyping array 2022-11-10 34804013 Chong AHW 2021-11-04 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34804013 Genetic Analyses of Common Infections in the Avon Longitudinal Study of Parents and Children Cohort. Anti-alpha-casein IgG levels 683 European ancestry individuals NA Illumina [NR] (imputed) 0 anti-alpha-casein IgG measurement http://www.ebi.ac.uk/efo/EFO_0801086 GCST90095171 Genome-wide genotyping array 2023-01-17 36271454 Khattab A 2022-10-21 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36271454 Nidogen-1 could play a role in diabetic kidney disease development in type 2 diabetes: a genome-wide association meta-analysis. Diabetic kidney disease in type 2 diabetes 5,141 European ancestry cases, 7,982 European ancestry controls NA NR [NR] 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90244670 Genome-wide genotyping array 2023-01-17 36271454 Khattab A 2022-10-21 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36271454 Nidogen-1 could play a role in diabetic kidney disease development in type 2 diabetes: a genome-wide association meta-analysis. Estimated glomerular filtration rate in type 2 diabetes 26,786 European ancestry individuals NA NR [NR] 2 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90244671 Genome-wide genotyping array 2023-01-17 36271454 Khattab A 2022-10-21 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36271454 Nidogen-1 could play a role in diabetic kidney disease development in type 2 diabetes: a genome-wide association meta-analysis. Estimated glomerular filtration rate in non-diabetics 339,080 European ancestry individuals NA NR [NR] 2 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90244672 Genome-wide genotyping array 2023-01-17 36271454 Khattab A 2022-10-21 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36271454 Nidogen-1 could play a role in diabetic kidney disease development in type 2 diabetes: a genome-wide association meta-analysis. Diabetic kidney disease in type 2 diabetes 8,486 European ancestry cases, 10,354 European ancestry controls NA NR [NR] 2 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90244673 Genome-wide genotyping array 2023-01-25 36395078 Clark R 2022-11-17 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36395078 Education interacts with genetic variants near GJD2, RBFOX1, LAMA2, KCNQ5 and LRRC4C to confer susceptibility to myopia. Refractive error (autorefraction measured) 88,334 European ancestry individuals NA Affymetrix [7000000] (imputed) 21 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST90244789 Genome-wide genotyping array 2022-11-01 36123890 Saita K 2022-09-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/36123890 Genetic polymorphism of pleiotrophin is associated with pain experience in Japanese adults: Case-control study. Cancer pain intensity 90 Japanese ancestry individuals NA Illumina [771433] 1 cancer pain http://www.ebi.ac.uk/efo/EFO_0801084 GCST90179178 Genome-wide genotyping array 2023-02-07 36653343 Ramo JT 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653343 Genome-wide screen of otosclerosis in population biobanks: 27 loci and shared associations with skeletal structure. Otosclerosis 3,504 European ancestry cases, 861,198 European ancestry controls NA Affymetrix, Illumina [13615309] (imputed) 52 otosclerosis http://www.ebi.ac.uk/efo/EFO_0004213 GCST90129575 Genome-wide genotyping array 2023-02-01 30747904 Freidin MB 2019-06-01 Pain www.ncbi.nlm.nih.gov/pubmed/30747904 Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals. Back pain 91,100 European ancestry cases, 258,900 European ancestry controls 28,284 European ancestry cases, 75,578 European ancestry controls, 2,520 South Asian ancestry cases, 4,639 South Asian ancestry controls, 2,414 African ancestry cases, 4,845 African ancestry controls, 401 Chinese ancestry cases, 1,084 Chinese ancestry controls NR [NR] (imputed) 10 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90245850 Genome-wide genotyping array 2023-02-01 30747904 Freidin MB 2019-06-01 Pain www.ncbi.nlm.nih.gov/pubmed/30747904 Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals. Back pain 119,384 European ancestry cases, 334,478 European ancestry controls NA NR [NR] (imputed) 23 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90245851 Genome-wide genotyping array 2023-02-09 36658081 Dueker N 2022-12-05 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/36658081 Genome-wide association study of executive function in a multi-ethnic cohort implicates LINC01362: Results from the northern Manhattan study. Executive function 747 Hispanic individuals, 181 African ancestry individuals, 149 European ancestry individuals NA Affymetrix [NR] (imputed) 4 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90245988 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Alpha-ketobutyrate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 alpha-ketobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800140 GCST90102869 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Alpha-ketoglutarate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90102870 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Alpha-tocopherol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90102871 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Andro steroid monosulfate (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 7 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90102872 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Androsterone glucuronide (X-22379) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 10 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90102873 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Androsterone sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90102874 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Arabitol/xylitol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 arabitol measurement, xylitol measurement http://www.ebi.ac.uk/efo/EFO_0800148, http://www.ebi.ac.uk/efo/EFO_0801067 GCST90102875 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Arabonate/xylonate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 xylonate measurement, arabonate measurement http://www.ebi.ac.uk/efo/EFO_0800147, http://www.ebi.ac.uk/efo/EFO_0801066 GCST90102876 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Arachidate (20:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 arachidate (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800625 GCST90102877 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Arachidonate (20:4n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90102878 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Arachidonoylcholine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 arachidonoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800478 GCST90102879 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Arginine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90102880 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ascorbic acid 3-sulfate (X-12206) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90102881 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Asparagine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90102882 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Aspartate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90102883 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Azelate (nonanedioate) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 azelate (C9-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800615 GCST90102884 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Behenoyl sphingomyelin (d18:1/22:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 behenoyl sphingomyelin (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800376 GCST90102885 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Benzoate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90102886 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Beta-citrylglutamate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 7 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90102887 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Beta-hydroxyisovalerate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90102888 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Betaine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90102889 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Bilirubin (E,E) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90102890 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Bilirubin (E,Z or Z,E) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90102891 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Bilirubin (z,z) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90102892 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Biliverdin levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90102893 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5alpha-androstan-3beta,17beta-diol disulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90102844 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800291 GCST90102845 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5alpha-pregnan-3beta,20alpha-diol disulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90102846 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800285 GCST90102847 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800284 GCST90102848 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-bromotryptophan levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 6-bromotryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800099 GCST90102849 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-dodecenoate (12:1n7) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 5-dodecenoate 12:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021100 GCST90102850 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-dodecenoylcarnitine (C12:1) (X-11540) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90102851 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-hydroxylysine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 5-hydroxylysine measurement http://www.ebi.ac.uk/efo/EFO_0800002 GCST90102852 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-methyluridine (ribothymidine) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90102853 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 5-oxoproline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90102854 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 6-hydroxyindole sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90102855 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 7-alpha-hydroxy-3-oxo-4-cholestenoate 7-Hoca measurement http://www.ebi.ac.uk/efo/EFO_0021116 GCST90102856 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 7-methylguanine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90102857 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 7-methylxanthine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90102858 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. 9-hydroxystearate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 9-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0800369 GCST90102859 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Acetylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90102860 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Aconitate [cis or trans] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90102861 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Adenine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Adenine measurement http://www.ebi.ac.uk/efo/EFO_0021573 GCST90102862 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Adenosine 5'-monophosphate (AMP) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Adenosine 5'-monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0021574 GCST90102863 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Adrenate (22:4n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90102864 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Alanine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90102865 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Allantoin levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90102866 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Alpha-hydroxyisocaproate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90102867 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Alpha-hydroxyisovalerate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90102868 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycochenodeoxycholate glucuronide (1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 10 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90102994 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycochenodeoxycholate sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Glycochenodeoxycholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022097 GCST90102995 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycocholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90102996 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycocholenate sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90102997 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycodeoxycholate sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Glycodeoxycholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022098 GCST90102998 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycolithocholate sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90102999 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800476 GCST90103000 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 glycosyl-N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800275 GCST90103001 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycoursodeoxycholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90103002 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Guanidinoacetate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90103003 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gulonate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90103004 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hexadecadienoate (16:2n6) (X-12450) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 hexadecadienoate (16:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800491 GCST90103005 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hexadecanedioate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90103006 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hexadecenedioate (c16:1-dc) (X-11905) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90103007 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hexanoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90103008 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hippurate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90103009 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Histidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90103010 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Homoarginine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST90103011 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Homocitrulline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90103012 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Homostachydrine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90103013 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hydantoin-5-propionic acid levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 Hydantoin-5-propionic acid measurement http://www.ebi.ac.uk/efo/EFO_0022099 GCST90103014 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hydroxy-cmpf (X-02269) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-02269 measurement http://www.ebi.ac.uk/efo/EFO_0021183 GCST90103015 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hypotaurine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90103016 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Hypoxanthine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90103017 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Imidazole lactate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90103018 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cyclo(pro-val) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Cyclo(pro-val) measurement http://www.ebi.ac.uk/efo/EFO_0022092 GCST90102919 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cys-gly, oxidized levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90102920 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cysteine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90102921 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cysteine s-sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90102922 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cysteine-glutathione disulfide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90102923 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cysteinylglycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90102924 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cystine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90102925 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cytidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90102926 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Decadienedioic acid (c10:2-dc) (X-21792) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 8 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90102927 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Decanoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90102928 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dehydroisoandrosterone sulfate (dhea-s) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 dehydroisoandrosterone sulfate DHEA-S measurement http://www.ebi.ac.uk/efo/EFO_0021119 GCST90102929 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Deoxycarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90102930 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Deoxycholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90102931 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Deoxycholic acid glucuronide (X-11491) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90102932 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Diacylglycerol (16:1/18:2 [2], 16:0/18:3 [1]) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 diacylglycerol (16:1/18:2 [2], 16:0/18:3 [1]) measurement http://www.ebi.ac.uk/efo/EFO_0800509 GCST90102933 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dihomo-linoleate (20:2n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90102934 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dihomo-linolenate (20:3n3 or n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90102935 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dimethylarginine (sdma + adma) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90102936 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dimethylglycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90102937 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Docosadienoate (22:2n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 docosadienoate (22:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800211 GCST90102938 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Docosadioate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 docosadioate (C22-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800331 GCST90102939 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Docosahexaenoate (DHA; 22:6n3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 docosahexaenoate DHA; 22:6n3 measurement http://www.ebi.ac.uk/efo/EFO_0021047 GCST90102940 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Docosapentaenoate (n3 DPA; 22:5n3) levels 8,809 European ancestry individuals, 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 docosapentaenoate n3 DPA; 22:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021048 GCST90102941 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Docosapentaenoate (n6 DPA; 22:5n6) levels NA Affymetrix [10000000] (imputed) 1 docosapentaenoate (n6 DPA; 22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800249 GCST90102942 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dodecadienoate (12:2) (X-21343) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 dodecadienoate (12:2) measurement http://www.ebi.ac.uk/efo/EFO_0800572 GCST90102943 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Iminodiacetate (IDA) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 iminodiacetate (IDA) measurement http://www.ebi.ac.uk/efo/EFO_0800945 GCST90103019 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Indoleacetate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90103020 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Indolelactate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90103021 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Indolepropionate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90103022 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Isobutyrylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90103023 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Isoleucine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90103024 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Isoleucylleucine/leucylisoleucine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 Isoleucylleucine/leucylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0022100 GCST90103025 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Isoursodeoxycholate (X-21666) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 isoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800315 GCST90103026 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Isovalerylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 isovalerylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020019 GCST90103027 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Kynurenate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90103028 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Kynurenine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90103029 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Lactate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90103030 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800429 GCST90103031 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Laurate (12:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90103032 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Laurylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90103033 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Leucine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90103034 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Linoleate (18:2n6) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90103035 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Linolenate [alpha or gamma; (18:3n3 or 6)] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90103036 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Linoleoyl ethanolamide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90103037 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800499 GCST90103038 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800500 GCST90103039 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Linoleoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90103040 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Linoleoyl-linoleoyl-glycerol (18:2/18:2) [1] levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 linoleoyl-linoleoyl-glycerol (18:2/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800510 GCST90103041 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Lithocholate sulfate (1) (X-17469) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 lithocholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800579 GCST90103042 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Lysine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90103043 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Branched chain 14:0 dicarboxylic acid (X-17145) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 branched chain 14:0 dicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0800593 GCST90102894 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) (X-23295) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) measurement http://www.ebi.ac.uk/efo/EFO_0800661 GCST90102895 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid (X-22764) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0800662 GCST90102896 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Butyrylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 butyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020010 GCST90102897 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Caffeine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90102898 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Caprate (10:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 caprate 10:0 measurement http://www.ebi.ac.uk/efo/EFO_0021101 GCST90102899 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Caproate (6:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 caproate 6:0 measurement http://www.ebi.ac.uk/efo/EFO_0021102 GCST90102900 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Caprylate (8:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 caprylate 8:0 measurement http://www.ebi.ac.uk/efo/EFO_0021103 GCST90102901 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Carnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90102902 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Catechol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90102903 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. C-glycosyltryptophan levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90102904 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90102905 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cholesterol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90102906 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Choline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90102907 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Choline phosphate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90102908 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cinnamoylglycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90102909 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cis-4-decenoate (10:1n6) (X-23293) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 8 cis-4-decenoate (10:1n6) measurement http://www.ebi.ac.uk/efo/EFO_0800318 GCST90102910 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cis-4-decenoyl carnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Cis-4-decenoyl carnitine measurement http://www.ebi.ac.uk/efo/EFO_0022091 GCST90102911 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Citrate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90102912 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Citrulline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90102913 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cortisol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90102914 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cortisone levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90102915 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Cortolone glucuronide (1) (X-17359) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90102916 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Creatine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90102917 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Creatinine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90102918 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dodecanedioate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90102944 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Dopamine sulfate (2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 Dopamine sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0022094 GCST90102945 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. EDTA levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 EDTA measurement http://www.ebi.ac.uk/efo/EFO_0800946 GCST90102946 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Eicosanodioate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 Eicosanodioate measurement http://www.ebi.ac.uk/efo/EFO_0022095 GCST90102947 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Eicosapentaenoate (EPA; 20:5n3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 eicosapentaenoate (EPA; 20:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800616 GCST90102948 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Eicosenoate (20:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 eicosenoate (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800220 GCST90102949 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Epiandrosterone sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90102950 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ergothioneine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90102951 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Erucate (22:1n9) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 erucate (22:1n9) measurement http://www.ebi.ac.uk/efo/EFO_0800601 GCST90102952 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Erythritol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90102953 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Erythronate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90102954 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ethyl alpha-glucopyranoside (X-24293) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 ethyl alpha-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801019 GCST90102955 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ethyl beta-glucopyranoside (X-23314) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90102956 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ethylmalonate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90102957 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Etiocholanolone glucuronide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 8 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90102958 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Fructose levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90102959 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Fumarate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90102960 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Galactonate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90102961 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-CEHC levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90102962 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamyl-alpha-lysine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90102963 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylcitrulline (X-24449) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 gamma-glutamylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800690 GCST90102964 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamyl-epsilon-lysine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 gamma-glutamyl-epsilon-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800667 GCST90102965 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylglutamate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90102966 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylglutamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90102967 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylglycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90102968 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylhistidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90102969 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylisoleucine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90102970 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylleucine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90102971 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylmethionine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90102972 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylphenylalanine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021142 GCST90102973 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylthreonine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90102974 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamyltyrosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90102975 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-glutamylvaline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90102976 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gamma-tocopherol/beta-tocopherol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 gamma-tocopherol measurement, beta-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007899, http://www.ebi.ac.uk/efo/EFO_0800168 GCST90102977 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gentisate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90102978 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Gluconate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90102979 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glucose levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90102980 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glucuronate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90102981 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glucuronide of piperine metabolite c17h21no3 (4) (X-01911) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90102982 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glutamate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90102983 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glutamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90102984 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glutamine conjugate of c6h10o2 (2) (X-12472) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90102985 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glutamine conjugate of c7h12o2 (X-17327) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glutamine conjugate of C7H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800656 GCST90102986 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glutarate (pentanedioate) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Glutarate (pentanedioate) measurement http://www.ebi.ac.uk/efo/EFO_0022096 GCST90102987 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycerate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90102988 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycerol levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90102989 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycerophosphoethanolamine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90102990 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycerophosphorylcholine (GPC) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90102991 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90102992 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Glycochenodeoxycholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90102993 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Thyroxine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90103219 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tiglylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90103220 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Trans-4-hydroxyproline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90103221 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tricosanoyl sphingomyelin (d18:1/23:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 tricosanoyl sphingomyelin (d18:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0800401 GCST90103222 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tridecenedioate (c13:1-dc) (X-11438) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 tridecenedioate (C13:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800309 GCST90103223 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Trigonelline (n'-methylnicotinate) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90103224 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Trimethylamine n-oxide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90103225 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tryptophan levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90103226 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tryptophan betaine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90103227 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tyrosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90103228 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Undecenoylcarnitine (c11:1) (X-17337) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90103229 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Uracil levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 uracil measurement http://www.ebi.ac.uk/efo/EFO_0800644 GCST90103230 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Urate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90103231 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Urea levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90103232 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Uridine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90103233 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ursodeoxycholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90103234 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Valine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90103235 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Vanillylmandelate (VMA) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90103236 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11261 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-11261 measurement http://www.ebi.ac.uk/efo/EFO_0021221 GCST90103237 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11299 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90103238 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11308 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-11308 measurement http://www.ebi.ac.uk/efo/EFO_0800693 GCST90103239 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11315 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90103240 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11372 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-11372 measurement http://www.ebi.ac.uk/efo/EFO_0800694 GCST90103241 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11381 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 8 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90103242 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11441 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-11441 measurement http://www.ebi.ac.uk/efo/EFO_0021235 GCST90103243 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Ribonate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 ribonate measurement http://www.ebi.ac.uk/efo/EFO_0800144 GCST90103169 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. S-1-pyrroline-5-carboxylate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90103170 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Salicylate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90103171 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sarcosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90103172 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Serine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90103173 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Serotonin levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90103174 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. S-methylcysteine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 S-methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800054 GCST90103175 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Spermidine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90103176 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphinganine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90103177 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphinganine-1-phosphate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 sphinganine-1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800274 GCST90103178 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 Sphingomyelin (d18:1/14:0, d16:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022105 GCST90103179 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/15:0, d16:1/17:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 Sphingomyelin (d18:1/15:0, d16:1/17:0) measurement http://www.ebi.ac.uk/efo/EFO_0022106 GCST90103180 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022107 GCST90103181 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Sphingomyelin (d18:1/18:1, d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0022108 GCST90103182 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 Sphingomyelin (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0022109 GCST90103183 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Sphingomyelin (d18:1/20:1, d18:2/20:0) measurement http://www.ebi.ac.uk/efo/EFO_0022110 GCST90103184 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0022111 GCST90103185 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022112 GCST90103186 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 Sphingomyelin (d18:1/24:1, d18:2/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0022113 GCST90103187 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:2/14:0, d18:1/14:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Sphingomyelin (d18:2/14:0, d18:1/14:1) measurement http://www.ebi.ac.uk/efo/EFO_0022114 GCST90103188 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Sphingomyelin (d18:2/16:0, d18:1/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0022115 GCST90103189 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022116 GCST90103190 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 Sphingomyelin (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0022117 GCST90103191 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingosine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90103192 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sphingosine 1-phosphate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90103193 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Stachydrine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90103194 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Stearate (18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90103195 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Stearidonate (18:4n3) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90103196 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Stearoyl sphingomyelin (d18:1/18:0) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 stearoyl sphingomyelin (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800611 GCST90103197 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Stearoylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90103198 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Succinate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90103199 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Succinimide levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 Succinimide measurement http://www.ebi.ac.uk/efo/EFO_0022118 GCST90103200 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Succinylcarnitine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 8 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90103201 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sulfate of piperine metabolite c16h19no3 (2) (X-11452) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90103202 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sulfate of piperine metabolite c16h19no3 (3) (X-12231) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90103203 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90103204 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tartronate (hydroxymalonate) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 tartronate (hydroxymalonate) measurement http://www.ebi.ac.uk/efo/EFO_0800944 GCST90103205 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Taurine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90103206 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Taurochenodeoxycholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90103207 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Taurocholate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90103208 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Taurocholenate sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90103209 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Taurolithocholate 3-sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90103210 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tetradecadienoate (14:2) (X-12442) levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 tetradecadienoate (14:2) measurement http://www.ebi.ac.uk/efo/EFO_0800570 GCST90103211 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Tetradecanedioate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90103212 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Theobromine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90103213 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Theophylline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90103214 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Thioproline levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90103215 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Threonate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90103216 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Threonine levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90103217 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. Thymol sulfate levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90103218 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11442 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-11442 measurement http://www.ebi.ac.uk/efo/EFO_0021236 GCST90103244 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11444 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 5 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90103245 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11470 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90103246 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11478 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90103247 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11483 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90103248 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11522 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-11522 measurement http://www.ebi.ac.uk/efo/EFO_0800696 GCST90103249 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11530 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-11530 measurement http://www.ebi.ac.uk/efo/EFO_0021249 GCST90103250 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11787 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90103251 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11795 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90103252 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11850 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90103253 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-11880 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-11880 measurement http://www.ebi.ac.uk/efo/EFO_0800698 GCST90103254 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12007 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90103255 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12100 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-12100 measurement http://www.ebi.ac.uk/efo/EFO_0800701 GCST90103256 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12101 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90103257 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12216 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90103258 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12462 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-12462 measurement http://www.ebi.ac.uk/efo/EFO_0800717 GCST90103259 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12524 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-12524 measurement http://www.ebi.ac.uk/efo/EFO_0021314 GCST90103260 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12680 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90103261 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12844 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90103262 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12847 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90103263 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-12849 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-12849 measurement http://www.ebi.ac.uk/efo/EFO_0800732 GCST90103264 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-13431 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90103265 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-13684 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90103266 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-13835 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-13835 measurement http://www.ebi.ac.uk/efo/EFO_0800743 GCST90103267 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-13866 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90103268 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21258 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-21258 measurement http://www.ebi.ac.uk/efo/EFO_0800802 GCST90103294 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21286 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-21286 measurement http://www.ebi.ac.uk/efo/EFO_0800804 GCST90103295 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21319 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90103296 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21339 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-21339 measurement http://www.ebi.ac.uk/efo/EFO_0800808 GCST90103297 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21353 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-21353 measurement http://www.ebi.ac.uk/efo/EFO_0800809 GCST90103298 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21358 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-21358 measurement http://www.ebi.ac.uk/efo/EFO_0022120 GCST90103299 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21364 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90103300 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21383 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-21383 measurement http://www.ebi.ac.uk/efo/EFO_0800812 GCST90103301 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21410 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 9 X-21410 measurement http://www.ebi.ac.uk/efo/EFO_0800813 GCST90103302 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21448 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-21448 measurement http://www.ebi.ac.uk/efo/EFO_0800816 GCST90103303 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21467 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 6 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90103304 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21658 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-21658 measurement http://www.ebi.ac.uk/efo/EFO_0022121 GCST90103305 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-21736 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-21736 measurement http://www.ebi.ac.uk/efo/EFO_0800821 GCST90103306 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-22162 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 1 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90103307 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-22771 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-22771 measurement http://www.ebi.ac.uk/efo/EFO_0800844 GCST90103308 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-22775 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-22775 measurement http://www.ebi.ac.uk/efo/EFO_0022122 GCST90103309 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23593 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-23593 measurement http://www.ebi.ac.uk/efo/EFO_0800851 GCST90103310 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23636 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-23636 measurement http://www.ebi.ac.uk/efo/EFO_0800852 GCST90103311 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23637 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-23637 measurement http://www.ebi.ac.uk/efo/EFO_0022123 GCST90103312 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23639 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 2 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90103313 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23644 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-23644 measurement http://www.ebi.ac.uk/efo/EFO_0800855 GCST90103314 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23652 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 0 X-23652 measurement http://www.ebi.ac.uk/efo/EFO_0022124 GCST90103315 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23680 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 4 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90103316 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23739 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90103317 Genome-wide genotyping array 2023-01-09 35050183 Hysi PG 2022-01-11 Metabolites www.ncbi.nlm.nih.gov/pubmed/35050183 Metabolome Genome-Wide Association Study Identifies 74 Novel Genomic Regions Influencing Plasma Metabolites Levels. X-23749 levels 8,809 European ancestry individuals NA Affymetrix [10000000] (imputed) 3 X-23749 measurement http://www.ebi.ac.uk/efo/EFO_0022125 GCST90103318 Genome-wide genotyping array 2022-09-21 35378236 Jami ES 2022-03-30 J Am Acad Child Adolesc Psychiatry www.ncbi.nlm.nih.gov/pubmed/35378236 Genome-wide Association Meta-analysis of Childhood and Adolescent Internalizing Symptoms. Internalizing symptoms during childhood and adolescence 64,641 European ancestry individuals NA Affymetrix, Illumina [5445944] (imputed) 0 internalizing disorder http://www.ebi.ac.uk/efo/EFO_0020971 GCST90054778 Genome-wide genotyping array 2022-08-25 35751511 Ghouse J 2022-06-25 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/35751511 Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci. ACE-inhibitor discontinuation 33,959 European ancestry cases who discontinued ACEi, 44,041 European ancestry controls who continued ACEi treatment NA Illumina [NR] (imputed) 7 response to angiotensin-converting enzyme inhibitor http://www.ebi.ac.uk/efo/EFO_0005325 GCST90132618 Genome-wide genotyping array 2022-10-25 34680977 Er LK 2021-10-07 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34680977 Genome-Wide Association Study on Adiponectin-Mediated Suppression of HDL-C Levels in Taiwanese Individuals Identifies Functional Haplotypes in CDH13. Adiponectin levels 2,199 Taiwanese ancestry individuals NA Affymetrix [614823] 1 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90086173 Genome-wide genotyping array 2022-10-25 34680977 Er LK 2021-10-07 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34680977 Genome-Wide Association Study on Adiponectin-Mediated Suppression of HDL-C Levels in Taiwanese Individuals Identifies Functional Haplotypes in CDH13. High density lipoprotein cholesterol levels 2,199 Taiwanese ancestry individuals NA Affymetrix [614823] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90086174 Genome-wide genotyping array 2022-10-25 34680977 Er LK 2021-10-07 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34680977 Genome-Wide Association Study on Adiponectin-Mediated Suppression of HDL-C Levels in Taiwanese Individuals Identifies Functional Haplotypes in CDH13. HDL cholesterol levels adjusted for adiponectin levels 2,199 Taiwanese ancestry individuals NA Affymetrix [614823] 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179134 Genome-wide genotyping array 2022-09-23 36046661 Liu L 2022-08-24 J Inflamm Res www.ncbi.nlm.nih.gov/pubmed/36046661 Whole Exome Sequencing Revealed Variants That Predict Pulmonary Artery Involvement in Patients with Takayasu Arteritis. Takayasu arteritis 200 Han Chinese ancestry cases, 1,675 Han Chinese ancestry controls NA Illumina [103516] 32 Takayasu arteritis http://www.ebi.ac.uk/efo/EFO_1001857 GCST90137503 Exome-wide sequencing 2022-09-09 35701873 Downie CG 2022-06-14 Circ Res www.ncbi.nlm.nih.gov/pubmed/35701873 Genome Wide Association Studies of Variant-by-Thiazide Interaction on Lipids Identifies a Novel Low-Density Lipoprotein Cholesterol Locus. LDL cholesterol x thiazide diuretic use interaction 394,444 European ancestry individuals NA Affymetrix [9971737] (imputed) 1 response to thiazide, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007981, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90134250 Genome-wide genotyping array 2022-09-09 35701873 Downie CG 2022-06-14 Circ Res www.ncbi.nlm.nih.gov/pubmed/35701873 Genome Wide Association Studies of Variant-by-Thiazide Interaction on Lipids Identifies a Novel Low-Density Lipoprotein Cholesterol Locus. Natural-log transformed triglycerides x thiazide diuretic use interaction 395,058 European ancestry individuals NA Affymetrix [9971814] (imputed) 0 triglyceride measurement, response to thiazide http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0007981 GCST90134251 Genome-wide genotyping array 2022-09-09 35701873 Downie CG 2022-06-14 Circ Res www.ncbi.nlm.nih.gov/pubmed/35701873 Genome Wide Association Studies of Variant-by-Thiazide Interaction on Lipids Identifies a Novel Low-Density Lipoprotein Cholesterol Locus. Total cholesterol x thiazide diuretic use interaction 395,096 European ancestry individuals NA Affymetrix [9971807] (imputed) 0 total cholesterol measurement, response to thiazide http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0007981 GCST90134252 Genome-wide genotyping array 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calpastatin levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 calpastatin measurement http://www.ebi.ac.uk/efo/EFO_0008065 GCST90161593 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ck-beta-8-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 Ck-beta-8-1 measurement http://www.ebi.ac.uk/efo/EFO_0008085 GCST90161594 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD209 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 17 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90161595 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-type lectin domain family 4 member M levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C-type lectin domain family 4 member M measurement http://www.ebi.ac.uk/efo/EFO_0020202 GCST90161596 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Follicle stimulating hormone levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90161597 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 galectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020397 GCST90161598 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glial fibrillary acidic protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90161599 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-19 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 interleukin 19 measurement http://www.ebi.ac.uk/efo/EFO_0008180 GCST90161600 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST90161601 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-X-C motif chemokine 11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90161602 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 C-C motif chemokine 3 measurement http://www.ebi.ac.uk/efo/EFO_0008051 GCST90161603 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-type mannose receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 C-type mannose receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020204 GCST90161604 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Myoglobin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 myoglobin measurement http://www.ebi.ac.uk/efo/EFO_0005057 GCST90161605 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SPARC levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90161606 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 18 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 C-C motif chemokine 18 measurement http://www.ebi.ac.uk/efo/EFO_0008046 GCST90161607 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pleiotrophin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pleiotrophin measurement http://www.ebi.ac.uk/efo/EFO_0020651 GCST90161608 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Resistin levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90161609 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Trypsin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 trypsin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020790 GCST90161610 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. von Willebrand factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90161611 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 6, soluble form levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tumor necrosis factor ligand superfamily member 6, soluble form measurement http://www.ebi.ac.uk/efo/EFO_0020797 GCST90161612 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fms-related tyrosine kinase 3 ligand levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90161613 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Haptoglobin levels 2,935 Qatari ancestry individuals NA NR [10004359] 28 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90161614 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-4 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-4 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020507 GCST90161615 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NKG2-D type II integral membrane protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 NKG2-D type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0008250 GCST90161616 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. WNT1-inducible-signaling pathway protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 WNT1-inducible-signaling pathway protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008321 GCST90161617 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sphingosine kinase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 sphingosine kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020751 GCST90162085 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbohydrate sulfotransferase 15 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90162086 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein-glutamine gamma-glutamyltransferase E levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein-glutamine gamma-glutamyltransferase e measurement http://www.ebi.ac.uk/efo/EFO_0020690 GCST90162087 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tropomyosin beta chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tropomyosin beta chain measurement http://www.ebi.ac.uk/efo/EFO_0020787 GCST90162088 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ubiquitin measurement http://www.ebi.ac.uk/efo/EFO_0020839 GCST90162089 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase ZAP-70 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 tyrosine-protein kinase ZAP-70 measurement http://www.ebi.ac.uk/efo/EFO_0020833 GCST90162090 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plasma protease C1 inhibitor levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90162091 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C3b levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement C3B measurement http://www.ebi.ac.uk/efo/EFO_0020275 GCST90162092 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 31 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST90162093 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C5b-C6 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement C5B-C6 complex measurement http://www.ebi.ac.uk/efo/EFO_0020279 GCST90162094 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90162095 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-3 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90162096 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-5 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 interleukin 5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008186 GCST90162097 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-11 measurement http://www.ebi.ac.uk/efo/EFO_0020490 GCST90162098 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kininogen-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 16 kininogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008198 GCST90162099 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage metalloelastase levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 macrophage metalloelastase measurement http://www.ebi.ac.uk/efo/EFO_0008220 GCST90162100 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neural cell adhesion molecule 1, 120 kDa isoform levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 neural cell adhesion molecule 1, 120 kda isoform measurement http://www.ebi.ac.uk/efo/EFO_0020593 GCST90162101 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet-derived growth factor subunit A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet-derived growth factor subunitAmeasurement http://www.ebi.ac.uk/efo/EFO_0020649 GCST90162102 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stem Cell Growth Factor-alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 stem cell growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020754 GCST90162103 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. A disintegrin and metalloproteinase with thrombospondin motifs 15 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 a disintegrin and metalloproteinase with thrombospondin motifs 15 measurement http://www.ebi.ac.uk/efo/EFO_0020123 GCST90162104 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Brain-specific serine protease 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 brain-specific serine protease 4 measurement http://www.ebi.ac.uk/efo/EFO_0020192 GCST90162105 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 19 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90162106 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chromobox protein homolog 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 chromobox protein homolog 5 measurement http://www.ebi.ac.uk/efo/EFO_0020258 GCST90162107 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cell adhesion molecule-related/down-regulated by oncogenes levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cell adhesion molecule-related/down-regulated by oncogenes measurement http://www.ebi.ac.uk/efo/EFO_0008079 GCST90162108 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Clusterin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007655 GCST90162109 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. A disintegrin and metalloproteinase with thrombospondin motifs 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90161643 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-L-iduronidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 18 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90161644 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Methionine aminopeptidase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 methionine aminopeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008232 GCST90161645 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Amyloid beta A4 protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 amyloid beta A4 protein measurement http://www.ebi.ac.uk/efo/EFO_0020145 GCST90161646 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Arylsulfatase B levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 arylsulfatase B measurement http://www.ebi.ac.uk/efo/EFO_0008030 GCST90161647 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. N-acylethanolamine-hydrolyzing acid amidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90161648 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. A disintegrin and metalloproteinase with thrombospondin motifs 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 a disintegrin and metalloproteinase with thrombospondin motifs 1 measurement http://www.ebi.ac.uk/efo/EFO_0021968 GCST90161649 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. A disintegrin and metalloproteinase with thrombospondin motifs 13 levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90161650 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 carbonic anhydrase 4 measurement http://www.ebi.ac.uk/efo/EFO_0020230 GCST90161651 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dipeptidyl peptidase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dipeptidyl peptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020325 GCST90161652 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lysosomal protective protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90161653 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin S levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90161654 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ectonucleoside triphosphate diphosphohydrolase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90161655 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coagulation Factor VII levels 2,935 Qatari ancestry individuals NA NR [10004359] 14 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST90161656 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 complement C2 measurement http://www.ebi.ac.uk/efo/EFO_0020274 GCST90161657 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cysteine-rich secretory protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cysteine-rich secretory protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020301 GCST90161658 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Enteropeptidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 enteropeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020349 GCST90161659 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. WAP, kazal, immunoglobulin, kunitz and NTR domain-containing protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 wap, kazal, immunoglobulin, kunitz and ntr domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020852 GCST90161660 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytosolic non-specific dipeptidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cytosolic non-specific dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020310 GCST90161661 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet glycoprotein VI levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 platelet glycoprotein VI measurement http://www.ebi.ac.uk/efo/EFO_0008263 GCST90161662 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granulysin levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90161663 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hyaluronan and proteoglycan link protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 hyaluronan and proteoglycan link protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020459 GCST90161664 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-degrading enzyme levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin-degrading enzyme measurement http://www.ebi.ac.uk/efo/EFO_0020472 GCST90161665 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Iduronate 2-sulfatase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 iduronate 2-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020461 GCST90161666 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 kallikrein-12 measurement http://www.ebi.ac.uk/efo/EFO_0008194 GCST90161667 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-13 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 kallikrein-13 measurement http://www.ebi.ac.uk/efo/EFO_0020512 GCST90161668 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90161669 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kremen protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 kremen protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020523 GCST90161670 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leukotriene A-4 hydrolase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 leukotriene a-4 hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020535 GCST90161671 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lymphatic vessel endothelial hyaluronic acid receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 lymphatic vessel endothelial hyaluronic acid receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020539 GCST90161672 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrilin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 matrilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020556 GCST90161673 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrix extracellular phosphoglycoprotein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 matrix extracellular phosphoglycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020557 GCST90161674 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Methionine aminopeptidase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 methionine aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020568 GCST90161675 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neutral ceramidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 17 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90161676 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Nidogen-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 nidogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008249 GCST90161677 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Polymeric immunoglobulin receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90161678 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glia-derived nexin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 glia-derived nexin measurement http://www.ebi.ac.uk/efo/EFO_0020403 GCST90161679 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proto-oncogene tyrosine-protein kinase receptor Ret levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 proto-oncogene tyrosine-protein kinase receptor Ret measurement http://www.ebi.ac.uk/efo/EFO_0008272 GCST90161680 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Secreted frizzled-related protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 secreted frizzled-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020718 GCST90161681 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Semaphorin-3A levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90161682 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tartrate-resistant acid phosphatase type 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90161683 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coiled-coil domain-containing protein 80 levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 coiled-coil domain-containing protein 80 measurement http://www.ebi.ac.uk/efo/EFO_0020268 GCST90161684 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90161685 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Aggrecan core protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 aggrecan core protein measurement http://www.ebi.ac.uk/efo/EFO_0020133 GCST90161686 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiopoietin-related protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 angiopoietin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020148 GCST90161687 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transforming growth factor-beta-induced protein ig-h3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 transforming growth factor-beta-induced protein ig-h3 measurement http://www.ebi.ac.uk/efo/EFO_0008302 GCST90161688 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Biglycan levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 biglycan measurement http://www.ebi.ac.uk/efo/EFO_0020182 GCST90161689 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 3-phosphoinositide-dependent protein kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 3-phosphoinositide-dependent protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020116 GCST90162082 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sialoadhesin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 sialoadhesin measurement http://www.ebi.ac.uk/efo/EFO_0020740 GCST90162083 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SPARC-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90162084 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Collagen alpha-1(XXIII) chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 collagen alpha-1(XXIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020270 GCST90162110 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Connective tissue-activating peptide III levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 connective tissue-activating peptide III measurement http://www.ebi.ac.uk/efo/EFO_0020285 GCST90162111 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitochondrial import inner membrane translocase subunit TIM14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitochondrial import inner membrane translocase subunit tim14 measurement http://www.ebi.ac.uk/efo/EFO_0020573 GCST90162112 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Adhesion G protein-coupled receptor E2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 adhesion G protein-coupled receptor E2 measurement http://www.ebi.ac.uk/efo/EFO_0021892 GCST90162113 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine-rich repeat transmembrane protein FLRT1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 leucine-rich repeat transmembrane protein FLRT1 measurement http://www.ebi.ac.uk/efo/EFO_0020533 GCST90162114 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galactoside 3(4)-L-fucosyltransferase levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 galactoside 3(4)-L-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0021853 GCST90162115 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-(1,3)-fucosyltransferase 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 alpha-(1;3)-fucosyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0021979 GCST90162116 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Adhesion G-protein coupled receptor G5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 adhesion G-protein coupled receptor G5 measurement http://www.ebi.ac.uk/efo/EFO_0021980 GCST90162117 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hepatoma-derived growth factor-related protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 hepatoma-derived growth factor-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020439 GCST90162118 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-34 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin-34 measurement http://www.ebi.ac.uk/efo/EFO_0020505 GCST90162119 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kin of IRRE-like protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 kin of IRRE-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020521 GCST90162120 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kynureninase levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 kynureninase measurement http://www.ebi.ac.uk/efo/EFO_0008201 GCST90162121 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Baculoviral IAP repeat-containing protein 7 Isoform beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 baculoviral IAP repeat-containing protein 7 isoform beta measurement http://www.ebi.ac.uk/efo/EFO_0020175 GCST90162122 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurexophilin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90162123 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 measurement http://www.ebi.ac.uk/efo/EFO_0020108 GCST90162124 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plexin-C1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 plexin-C1 measurement http://www.ebi.ac.uk/efo/EFO_0008266 GCST90162125 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. R-spondin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 r-spondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020696 GCST90162126 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SH2 domain-containing protein 1A levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 sh2 domain-containing protein 1a measurement http://www.ebi.ac.uk/efo/EFO_0020737 GCST90162127 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SLIT and NTRK-like protein 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 slit and ntrk-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020743 GCST90162128 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. VPS10 domain-containing receptor SorCS2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 vps10 domain-containing receptor sorcs2 measurement http://www.ebi.ac.uk/efo/EFO_0020851 GCST90162129 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pancreatic hormone levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pancreatic hormone measurement http://www.ebi.ac.uk/efo/EFO_0020621 GCST90162130 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90162131 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 3-hydroxyisobutyrate dehydrogenase, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 3-hydroxyisobutyrate dehydrogenase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020115 GCST90162132 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granulocyte-macrophage colony-stimulating factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 granulocyte-macrophage colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0020417 GCST90162133 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lymphotoxin-alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lymphotoxin-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020544 GCST90162134 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bone morphogenetic protein receptor type-1A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bone morphogenetic protein receptor type-1a measurement http://www.ebi.ac.uk/efo/EFO_0020188 GCST90162160 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bone morphogenetic protein receptor type-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bone morphogenetic protein receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020189 GCST90162161 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. BDNF/NT-3 growth factors receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bdnf/nt-3 growth factors receptor measurement http://www.ebi.ac.uk/efo/EFO_0020179 GCST90162162 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vascular endothelial growth factor A, isoform 121 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 vascular endothelial growth factor A, isoform 121 measurement http://www.ebi.ac.uk/efo/EFO_0020847 GCST90162163 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiogenin levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90162164 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coagulation factor IX levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 coagulation factor IX measurement http://www.ebi.ac.uk/efo/EFO_0020263 GCST90162165 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coagulation Factor X levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 coagulation factor X measurement http://www.ebi.ac.uk/efo/EFO_0020265 GCST90162166 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth/differentiation factor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 growth/differentiation factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020428 GCST90162167 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90162168 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST90162169 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein Wnt-7a levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein wnt-7a measurement http://www.ebi.ac.uk/efo/EFO_0020689 GCST90162170 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Corticotropin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 corticotropin measurement http://www.ebi.ac.uk/efo/EFO_0020289 GCST90162171 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glucagon levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90162172 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C3a anaphylatoxin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C3a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020207 GCST90162173 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcineurin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calcineurin measurement http://www.ebi.ac.uk/efo/EFO_0008061 GCST90162174 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Caspase-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 caspase-2 measurement http://www.ebi.ac.uk/efo/EFO_0020240 GCST90162175 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coactosin-like protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 coactosin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020262 GCST90162176 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coagulation Factor V levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST90162177 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. D-dimer levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 d-dimer measurement http://www.ebi.ac.uk/efo/EFO_0020313 GCST90162178 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endoglin levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 endoglin measurement http://www.ebi.ac.uk/efo/EFO_0008118 GCST90162179 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 galectin-8 measurement http://www.ebi.ac.uk/efo/EFO_0020399 GCST90162180 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phospholipase A2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90162181 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glutathione S-transferase P levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90162182 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Aspartate aminotransferase, cytoplasmic levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 aspartate aminotransferase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0008031 GCST90162183 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 16 levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90162184 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Acidic leucine-rich nuclear phosphoprotein 32 family member B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 acidic leucine-rich nuclear phosphoprotein 32 family member b measurement http://www.ebi.ac.uk/efo/EFO_0020125 GCST90162011 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cofilin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cofilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020267 GCST90162012 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vacuolar protein sorting-associated protein VTA1 homolog levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 vacuolar protein sorting-associated protein VTA1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020845 GCST90162013 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Epidermal growth factor receptor substrate 15-like 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 epidermal growth factor receptor substrate 15-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020360 GCST90162014 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 3-hydroxyacyl-CoA dehydrogenase type-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 3-hydroxyacyl-coa dehydrogenase type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020114 GCST90162015 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Fer levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase FER measurement http://www.ebi.ac.uk/efo/EFO_0020821 GCST90162016 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heterogeneous nuclear ribonucleoprotein Q levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 heterogeneous nuclear ribonucleoprotein q measurement http://www.ebi.ac.uk/efo/EFO_0020443 GCST90162017 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Eukaryotic translation initiation factor 4 gamma 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 eukaryotic translation initiation factor 4 gamma 2 measurement http://www.ebi.ac.uk/efo/EFO_0020367 GCST90162018 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor 1 receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin-like growth factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020473 GCST90162019 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 receptor-like 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 19 interleukin 1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008168 GCST90162020 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine carboxyl methyltransferase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 leucine carboxyl methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008207 GCST90162021 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein lin-7 homolog B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein lin-7 homolog B measurement http://www.ebi.ac.uk/efo/EFO_0021978 GCST90162022 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pyruvate kinase PKM levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pyruvate kinase pkm measurement http://www.ebi.ac.uk/efo/EFO_0020695 GCST90162023 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. E3 ubiquitin-protein ligase Mdm2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 e3 ubiquitin-protein ligase mdm2 measurement http://www.ebi.ac.uk/efo/EFO_0020340 GCST90162024 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neural cell adhesion molecule L1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neural cell adhesion molecule L1 measurement http://www.ebi.ac.uk/efo/EFO_0020594 GCST90162025 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Nucleoside diphosphate kinase B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 nucleoside diphosphate kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020615 GCST90162026 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NSFL1 cofactor p47 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 NFSL1 cofactor p47 measurement http://www.ebi.ac.uk/efo/EFO_0020612 GCST90162027 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NudC domain-containing protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 NudC domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020616 GCST90162028 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proliferation-associated protein 2G4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proliferation-associated protein 2g4 measurement http://www.ebi.ac.uk/efo/EFO_0020658 GCST90162029 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serum paraoxonase/arylesterase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serum paraoxonase/arylesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020736 GCST90162030 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pescadillo homolog levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pescadillo homolog measurement http://www.ebi.ac.uk/efo/EFO_0020633 GCST90162031 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prefoldin subunit 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 prefoldin subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0020652 GCST90162032 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glucose-6-phosphate isomerase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glucose-6-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020407 GCST90162033 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phosphatidylethanolamine-binding protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 phosphatidylethanolamine-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020634 GCST90162034 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein disulfide-isomerase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein disulfide-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020669 GCST90162035 Genome-wide sequencing 2022-09-09 35912095 Huang Y 2022-07-15 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/35912095 Patterns of Convergence and Divergence Between Bipolar Disorder Type I and Type II: Evidence From Integrative Genomic Analyses. Bipolar disorder type I or bipolar disorder type II (pleiotropy) 25,060 European ancestry BDI cases, 6,781 European ancestry BDII cases, up to 814,053 European ancestry controls NA NR [NR] 0 bipolar II disorder, bipolar I disorder http://www.ebi.ac.uk/efo/EFO_0009964, http://www.ebi.ac.uk/efo/EFO_0009963 GCST90134565 Genome-wide genotyping array 2022-09-09 35912095 Huang Y 2022-07-15 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/35912095 Patterns of Convergence and Divergence Between Bipolar Disorder Type I and Type II: Evidence From Integrative Genomic Analyses. Bipolar disorder type I vs bipolar disorder type II 25,060 European ancestry BDI cases, 6,781 European ancestry BDII cases NA NR [NR] 1 bipolar II disorder, bipolar I disorder http://www.ebi.ac.uk/efo/EFO_0009964, http://www.ebi.ac.uk/efo/EFO_0009963 GCST90134566 Genome-wide genotyping array 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proteasome subunit alpha type-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proteasome subunit alpha type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020664 GCST90162036 Genome-wide sequencing 2022-09-05 35770850 Chung J 2022-06-30 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/35770850 Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women. Alzheimer's disease 5 Hutterite (founder/genetic isolate) cases, 26 Hutterite (founder/genetic isolate) controls NA Affymetrix [4807330] (imputed) 22 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90134416 Genome-wide genotyping array 2022-09-05 35770850 Chung J 2022-06-30 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/35770850 Genome-wide association and multi-omics studies identify MGMT as a novel risk gene for Alzheimer's disease among women. Alzheimer's disease in APOE e4- carriers 3,399 European ancestry female cases, 6,905 European ancestry female controls NA NR [NR] (imputed) 4 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90134415 Genome-wide genotyping array 2022-11-16 34791242 Knol MJ 2021-11-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34791242 Genetic architecture of orbital telorism. Orbital telorism 34,130 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 72 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90239648 Genome-wide genotyping array 2022-09-09 35788059 Buch S 2022-07-04 Gut www.ncbi.nlm.nih.gov/pubmed/35788059 Genetic variation in TERT modifies the risk of hepatocellular carcinoma in alcohol-related cirrhosis: results from a genome-wide case-control study. Hepatocellular carcinoma in alcohol related cirrhosis 1,066 European ancestry cases, 844 European ancestry controls 148 European ancestry cases, 1,022 European ancestry controls Illumina [7946762] (imputed) 3 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90134423 Genome-wide genotyping array 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Erythropoietin receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 erythropoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020364 GCST90161442 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granulocyte colony-stimulating factor receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 granulocyte colony-stimulating factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020416 GCST90161443 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-37 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin-37 measurement http://www.ebi.ac.uk/efo/EFO_0020506 GCST90161444 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Laminin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 laminin measurement http://www.ebi.ac.uk/efo/EFO_0020528 GCST90161445 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. MHC class I polypeptide-related sequence A levels 2,935 Qatari ancestry individuals NA NR [10004359] 57 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST90161446 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NADPH--cytochrome P450 reductase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 NADPH--cytochrome P450 reductase measurement http://www.ebi.ac.uk/efo/EFO_0008242 GCST90161447 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Homeobox protein NANOG levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 homeobox protein nanog measurement http://www.ebi.ac.uk/efo/EFO_0020456 GCST90161448 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Natural cytotoxicity triggering receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 natural cytotoxicity triggering receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020589 GCST90161449 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein NOV homolog levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein nov homolog measurement http://www.ebi.ac.uk/efo/EFO_0020685 GCST90161450 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sialic acid-binding Ig-like lectin 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 sialic acid-binding Ig-like lectin 6 measurement http://www.ebi.ac.uk/efo/EFO_0008285 GCST90161451 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sialic acid-binding Ig-like lectin 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90161452 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sonic hedgehog protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 sonic hedgehog protein measurement http://www.ebi.ac.uk/efo/EFO_0020746 GCST90161453 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Immunoglobulin G levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 immunoglobulin G measurement http://www.ebi.ac.uk/efo/EFO_0020465 GCST90161454 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytokine receptor-like factor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytokine receptor-like factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020306 GCST90161455 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NKG2D ligand 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 NKG2-D ligand 3 measurement http://www.ebi.ac.uk/efo/EFO_0020611 GCST90161456 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inhibin beta A chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 inhibin beta A chain measurement http://www.ebi.ac.uk/efo/EFO_0020469 GCST90161457 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein A-I levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90161458 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Azurocidin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 azurocidin measurement http://www.ebi.ac.uk/efo/EFO_0020170 GCST90161459 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth/differentiation factor 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 growth/differentiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020429 GCST90161460 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C1q subcomponent levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90161461 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90161462 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Annexin A1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 annexin A1 measurement http://www.ebi.ac.uk/efo/EFO_0008026 GCST90162200 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Annexin A2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 annexin A2 measurement http://www.ebi.ac.uk/efo/EFO_0008027 GCST90162201 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cerebral dopamine neurotrophic factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90162202 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. cAMP-regulated phosphoprotein 19 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cAMP-regulated phosphoprotein 19 measurement http://www.ebi.ac.uk/efo/EFO_0020223 GCST90162203 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Junctional adhesion molecule B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 junctional adhesion molecule B measurement http://www.ebi.ac.uk/efo/EFO_0020509 GCST90161580 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. GTP-binding nuclear protein Ran levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 GTP-binding nuclear protein ran measurement http://www.ebi.ac.uk/efo/EFO_0020431 GCST90162037 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. RNA-binding protein 39 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 rna-binding protein 39 measurement http://www.ebi.ac.uk/efo/EFO_0020712 GCST90162038 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-soluble NSF attachment protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 alpha-soluble NSF attachment protein measurement http://www.ebi.ac.uk/efo/EFO_0020140 GCST90162039 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sphingosine kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 sphingosine kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020750 GCST90162040 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Spondin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90162041 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thymidine kinase, cytosolic levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thymidine kinase, cytosolic measurement http://www.ebi.ac.uk/efo/EFO_0020773 GCST90162042 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ligand-dependent nuclear receptor corepressor-like protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ligand-dependent nuclear receptor corepressor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020536 GCST90162043 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transketolase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transketolase measurement http://www.ebi.ac.uk/efo/EFO_0020783 GCST90162044 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Triosephosphate isomerase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 triosephosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020785 GCST90162045 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. dCTP pyrophosphatase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 DCTP pyrophosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020314 GCST90162046 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein phosphatase non-receptor type 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein phosphatase non-receptor type 6 measurement http://www.ebi.ac.uk/efo/EFO_0020837 GCST90162047 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein amnionless levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein amnionless measurement http://www.ebi.ac.uk/efo/EFO_0020667 GCST90162048 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cystatin-SA levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 cystatin-SA measurement http://www.ebi.ac.uk/efo/EFO_0008105 GCST90162049 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Brother of CDO levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 brother of CDO measurement http://www.ebi.ac.uk/efo/EFO_0020194 GCST90162050 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-type lectin domain family 1 member B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C-type lectin domain family 1 member B measurement http://www.ebi.ac.uk/efo/EFO_0020200 GCST90162051 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serum amyloid A-1 protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 18 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90162052 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-reactive protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90162053 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Intercellular adhesion molecule 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 25 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST90162054 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Death-associated protein kinase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 death-associated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008107 GCST90162055 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dual specificity tyrosine-phosphorylation-regulated kinase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dual specificity tyrosine-phosphorylation-regulated kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020337 GCST90162056 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth/differentiation factor 15 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90162057 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Desert hedgehog protein N-product levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 desert hedgehog protein n-product measurement http://www.ebi.ac.uk/efo/EFO_0020319 GCST90162058 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 12 measurement http://www.ebi.ac.uk/efo/EFO_0020377 GCST90162059 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 16 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90162060 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Properdin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 properdin measurement http://www.ebi.ac.uk/efo/EFO_0008269 GCST90161555 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vitamin K-dependent protein C levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90161556 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Parathyroid hormone-related protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 parathyroid hormone-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020622 GCST90161557 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stem Cell Growth Factor-beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 stem Cell Growth Factor beta measurement http://www.ebi.ac.uk/efo/EFO_0008292 GCST90161558 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vascular cell adhesion protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 vascular cell adhesion protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020846 GCST90161559 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 15 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90161560 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase receptor R3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase receptor R3 measurement http://www.ebi.ac.uk/efo/EFO_0020733 GCST90161561 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Amphiregulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 amphiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020144 GCST90161562 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bone morphogenetic protein 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bone morphogenetic protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020187 GCST90161563 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet glycoprotein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 platelet glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008262 GCST90161564 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Contactin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 contactin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020286 GCST90161565 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Connective tissue growth factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 connective tissue growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020284 GCST90161566 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Desmoglein-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 desmoglein-1 measurement http://www.ebi.ac.uk/efo/EFO_0020321 GCST90161567 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member EDAR levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 tumor necrosis factor receptor superfamily member EDAR measurement http://www.ebi.ac.uk/efo/EFO_0008310 GCST90161568 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-X-C motif chemokine 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C-X-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008058 GCST90161569 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endothelial cell-selective adhesion molecule levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90161570 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 galectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020398 GCST90161571 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth-regulated alpha protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 16 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST90161572 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Gro-beta/gamma levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 gro-beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0020422 GCST90161573 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone H1.2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone H1.2 measurement http://www.ebi.ac.uk/efo/EFO_0021966 GCST90161574 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inducible T-cell costimulator levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 inducible T-cell costimulator measurement http://www.ebi.ac.uk/efo/EFO_0021967 GCST90161575 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 receptor type 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90161576 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-17 receptor A levels 2,935 Qatari ancestry individuals NA NR [10004359] 13 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90161577 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-18 receptor accessory protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin 18 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008179 GCST90161578 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 receptor-like 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 interleukin 1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0008169 GCST90161579 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-1-antichymotrypsin levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 alpha-1-antichymotrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008019 GCST90161530 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement component C7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90161531 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cardiotrophin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cardiotrophin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020235 GCST90161532 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 28 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-C motif chemokine 28 measurement http://www.ebi.ac.uk/efo/EFO_0020199 GCST90161533 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. B-cell receptor CD22 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 B-cell receptor CD22 measurement http://www.ebi.ac.uk/efo/EFO_0020171 GCST90161534 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 21 C-C motif chemokine 14 measurement http://www.ebi.ac.uk/efo/EFO_0008042 GCST90161535 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin 4 measurement http://www.ebi.ac.uk/efo/EFO_0008184 GCST90161536 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Midkine levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 midkine measurement http://www.ebi.ac.uk/efo/EFO_0020571 GCST90161537 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 23 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90161538 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proliferating cell nuclear antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proliferating cell nuclear antigen measurement http://www.ebi.ac.uk/efo/EFO_0020657 GCST90161539 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90161540 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plasminogen activator inhibitor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90161541 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein E (isoform E3) levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 apolipoprotein E (isoform E3) measurement http://www.ebi.ac.uk/efo/EFO_0020157 GCST90161542 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein E (isoform E4) levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 apolipoprotein E (isoform E4) measurement http://www.ebi.ac.uk/efo/EFO_0020158 GCST90161543 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Artemin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 artemin measurement http://www.ebi.ac.uk/efo/EFO_0020162 GCST90161544 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytochrome c levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cytochrome C measurement http://www.ebi.ac.uk/efo/EFO_0020302 GCST90161545 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytochrome P450 3A4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytochrome p450 3a4 measurement http://www.ebi.ac.uk/efo/EFO_0020303 GCST90161546 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neuroblastoma suppressor of tumorigenicity 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neuroblastoma suppressor of tumorigenicity 1 measurement http://www.ebi.ac.uk/efo/EFO_0020598 GCST90161547 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Estrogen receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 estrogen receptor measurement http://www.ebi.ac.uk/efo/EFO_0008125 GCST90161548 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement factor D levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90161549 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth hormone receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 growth hormone receptor measurement http://www.ebi.ac.uk/efo/EFO_0020426 GCST90161550 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Group 10 secretory phospholipase A2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 group 10 secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020423 GCST90161551 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor-binding protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin-like growth factor-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020476 GCST90161552 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor I levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST90161553 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Luteinizing hormone levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90161554 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Retinoblastoma-associated protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 retinoblastoma-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0020706 GCST90162254 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 40S ribosomal protein S3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 40s ribosomal protein S3 measurement http://www.ebi.ac.uk/efo/EFO_0020117 GCST90162255 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Scavenger receptor cysteine-rich type 1 protein M130 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 scavenger receptor cysteine-rich type 1 protein m130 measurement http://www.ebi.ac.uk/efo/EFO_0020717 GCST90162256 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prolyl endopeptidase FAP levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 prolyl endopeptidase FAP measurement http://www.ebi.ac.uk/efo/EFO_0021856 GCST90162257 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NAD-dependent protein deacetylase sirtuin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 NAD-dependent protein deacetylase sirtuin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008241 GCST90162258 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Spectrin alpha chain, non-erythrocytic 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 spectrin alpha chain, non-erythrocytic 1 measurement http://www.ebi.ac.uk/efo/EFO_0020749 GCST90162259 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. FACT complex subunit SSRP1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fact complex subunit ssrp1 measurement http://www.ebi.ac.uk/efo/EFO_0020371 GCST90162260 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tropomyosin alpha-1 chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tropomyosin alpha-1 chain measurement http://www.ebi.ac.uk/efo/EFO_0020786 GCST90162261 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C3a anaphylatoxin des Arginine levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C3a anaphylatoxin des arginine measurement http://www.ebi.ac.uk/efo/EFO_0020206 GCST90161463 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein FAM107A levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 protein fam107a measurement http://www.ebi.ac.uk/efo/EFO_0020673 GCST90161464 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 18 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 18 measurement http://www.ebi.ac.uk/efo/EFO_0020380 GCST90161465 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 19 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90161466 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 20 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 20 measurement http://www.ebi.ac.uk/efo/EFO_0020381 GCST90161467 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020387 GCST90161468 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth/differentiation factor 11/8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 growth/differentiation factor 11/8 measurement http://www.ebi.ac.uk/efo/EFO_0021962 GCST90161469 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hemopexin levels 2,935 Qatari ancestry individuals NA NR [10004359] 26 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90161470 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 C-C motif chemokine 1 measurement http://www.ebi.ac.uk/efo/EFO_0008041 GCST90161471 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor-binding protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90161472 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90161473 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-16 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin 16 measurement http://www.ebi.ac.uk/efo/EFO_0008173 GCST90161474 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-17F levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin-17F measurement http://www.ebi.ac.uk/efo/EFO_0021963 GCST90161475 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-22 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90161476 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lactotransferrin levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 lactotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020526 GCST90161477 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 4-like levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 C-C motif chemokine 4-like measurement http://www.ebi.ac.uk/efo/EFO_0021848 GCST90161478 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 3-like 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 C-C motif chemokine 3-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008052 GCST90161479 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hepatocyte growth factor receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 hepatocyte growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0008153 GCST90161505 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrix metalloproteinase-17 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 matrix metalloproteinase-17 measurement http://www.ebi.ac.uk/efo/EFO_0020560 GCST90161506 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor ligand superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020796 GCST90161507 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Secreted frizzled-related protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90161508 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kunitz-type protease inhibitor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 Kunitz-type protease inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008200 GCST90161509 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase receptor Tie-1, soluble levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 tyrosine-protein kinase receptor Tie-1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008312 GCST90161510 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin+1, truncated mutation for UbB levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ubiquitin+1, truncated mutation for UBB measurement http://www.ebi.ac.uk/efo/EFO_0020844 GCST90161511 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Wnt inhibitory factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 wnt inhibitory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020853 GCST90161512 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Allograft inflammatory factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 allograft inflammatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020135 GCST90161513 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C5a anaphylatoxin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C5a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020208 GCST90161514 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase Chk1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase Chk1 measurement http://www.ebi.ac.uk/efo/EFO_0021965 GCST90161515 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 mitogen-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020579 GCST90161516 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glucocorticoid receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glucocorticoid receptor measurement http://www.ebi.ac.uk/efo/EFO_0020405 GCST90161517 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone acetyltransferase type B catalytic subunit levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone acetyltransferase type b catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0020452 GCST90161518 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone deacetylase 8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone deacetylase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020453 GCST90161519 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Importin subunit alpha-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 importin subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020467 GCST90161520 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dual specificity mitogen-activated protein kinase kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dual specificity mitogen-activated protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020335 GCST90161521 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone acetyltransferase KAT6A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone acetyltransferase kat6a measurement http://www.ebi.ac.uk/efo/EFO_0020451 GCST90161522 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein kinase C delta type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein kinase c delta type measurement http://www.ebi.ac.uk/efo/EFO_0020679 GCST90161523 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ras-related C3 botulinum toxin substrate 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ras-related c3 botulinum toxin substrate 1 measurement http://www.ebi.ac.uk/efo/EFO_0020699 GCST90161524 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. DNA repair protein RAD51 homolog 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 DNA repair protein rad51 homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0020330 GCST90161525 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. TATA-box-binding protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tata-box-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020764 GCST90161526 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. DNA topoisomerase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 DNA topoisomerase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020331 GCST90161527 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SUMO-conjugating enzyme UBC9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 sumo-conjugating enzyme UBC9 measurement http://www.ebi.ac.uk/efo/EFO_0020757 GCST90161528 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Yes levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase YES measurement http://www.ebi.ac.uk/efo/EFO_0020832 GCST90161529 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 C-C motif chemokine 8 measurement http://www.ebi.ac.uk/efo/EFO_0008055 GCST90161480 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stromelysin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 stromelysin‐1 measurement http://www.ebi.ac.uk/efo/EFO_0010608 GCST90161481 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrilysin levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 matrilysin measurement http://www.ebi.ac.uk/efo/EFO_0008227 GCST90161482 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neutrophil-activating peptide 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neutrophil-activating peptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020606 GCST90161483 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Superoxide dismutase [Cu-Zn] levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 superoxide dismutase [Cu-Zn] measurement http://www.ebi.ac.uk/efo/EFO_0020758 GCST90161484 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibrinogen levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90161485 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein B levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90161486 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiotensin-converting enzyme 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 angiotensin-converting enzyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0020150 GCST90161487 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Activin receptor type-1B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 activin receptor type-1B measurement http://www.ebi.ac.uk/efo/EFO_0020127 GCST90161488 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. A disintegrin and metalloproteinase with thrombospondin motifs 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 a disintegrin and metalloproteinase with thrombospondin motifs 4 measurement http://www.ebi.ac.uk/efo/EFO_0020124 GCST90161489 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiopoietin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 angiopoietin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020146 GCST90161490 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Agouti-related protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90161491 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Basal Cell Adhesion Molecule levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 basal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008032 GCST90161492 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cadherin-5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 cadherin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008060 GCST90161493 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD97 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 CD97 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020250 GCST90161494 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. COMM domain-containing protein 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 COMM domain-containing protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020273 GCST90161495 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ectodysplasin-A, secreted form levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ectodysplasin-a, secreted form measurement http://www.ebi.ac.uk/efo/EFO_0020341 GCST90161496 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fractalkine levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fractalkine measurement http://www.ebi.ac.uk/efo/EFO_0020395 GCST90161497 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kunitz-type protease inhibitor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 Kunitz-type protease inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008199 GCST90161498 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-27 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-27 measurement http://www.ebi.ac.uk/efo/EFO_0010916 GCST90161499 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. kallikrein-11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90161500 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 kallikrein-4 measurement http://www.ebi.ac.uk/efo/EFO_0020514 GCST90161501 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90161502 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. X-ray repair cross-complementing protein 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 x-ray repair cross-complementing protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020855 GCST90161503 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neutrophil gelatinase-associated lipocalin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neutrophil gelatinase-associated lipocalin measurement http://www.ebi.ac.uk/efo/EFO_0021964 GCST90161504 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low-density lipoprotein receptor-related protein 1B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 low-density lipoprotein receptor-related protein 1B measurement http://www.ebi.ac.uk/efo/EFO_0021873 GCST90162489 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Myosin-binding protein C; slow-type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 myosin-binding protein C; slow-type measurement http://www.ebi.ac.uk/efo/EFO_0022013 GCST90162490 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. N-terminal pro-BNP levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 N-terminal pro-BNP measurement http://www.ebi.ac.uk/efo/EFO_0022014 GCST90162491 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tropomyosin alpha-4 chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tropomyosin alpha-4 chain measurement http://www.ebi.ac.uk/efo/EFO_0022015 GCST90162492 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pituitary adenylate cyclase-activating polypeptide 27 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pituitary adenylate cyclase-activating polypeptide 27 measurement http://www.ebi.ac.uk/efo/EFO_0020640 GCST90162493 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Appetite-regulating hormone levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 appetite-regulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0022016 GCST90162494 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pituitary adenylate cyclase-activating polypeptide 38 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pituitary adenylate cyclase-activating polypeptide 38 measurement http://www.ebi.ac.uk/efo/EFO_0020641 GCST90162495 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 kallikrein‐6 measurement http://www.ebi.ac.uk/efo/EFO_0010622 GCST90161794 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C1r subcomponent levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 complement C1r subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008090 GCST90161690 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase-related protein 10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 carbonic anhydrase-related protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020233 GCST90161691 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD109 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 CD109 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008076 GCST90161692 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low affinity immunoglobulin epsilon Fc receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 low affinity immunoglobulin epsilon Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0008210 GCST90161693 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD48 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 CD48 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020247 GCST90161694 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD5 antigen-like levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 CD5 antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0020248 GCST90161695 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cryptic protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cryptic protein measurement http://www.ebi.ac.uk/efo/EFO_0020293 GCST90161696 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Contactin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90161697 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Contactin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 contactin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020287 GCST90161698 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Contactin-5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 contactin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008101 GCST90161699 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cystatin-F levels 2,935 Qatari ancestry individuals NA NR [10004359] 19 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90161700 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cystatin-M levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90161701 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Delta-like protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 delta-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020317 GCST90161702 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low affinity immunoglobulin gamma Fc region receptor II-a levels 2,935 Qatari ancestry individuals NA NR [10004359] 27 low affinity immunoglobulin gamma Fc region receptor II-a measurement http://www.ebi.ac.uk/efo/EFO_0021969 GCST90161703 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low affinity immunoglobulin gamma Fc region receptor II-b levels 2,935 Qatari ancestry individuals NA NR [10004359] 31 low affinity immunoglobulin gamma Fc region receptor II-b measurement http://www.ebi.ac.uk/efo/EFO_0021970 GCST90161704 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low affinity immunoglobulin gamma Fc region receptor III-B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 low affinity immunoglobulin gamma Fc region receptor III-B measurement http://www.ebi.ac.uk/efo/EFO_0008212 GCST90161705 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. High affinity immunoglobulin gamma Fc receptor I levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 high affinity immunoglobulin gamma fc receptor i measurement http://www.ebi.ac.uk/efo/EFO_0020447 GCST90161706 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Eukaryotic translation initiation factor 5A-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 eukaryotic translation initiation factor 5A-1 measurement http://www.ebi.ac.uk/efo/EFO_0020370 GCST90162464 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Gastrin-releasing peptide levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 gastrin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0022000 GCST90162465 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histidine triad nucleotide-binding protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histidine triad nucleotide-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020450 GCST90162466 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heat shock cognate 71 kDa protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heat shock cognate 71 kda protein measurement http://www.ebi.ac.uk/efo/EFO_0020434 GCST90162467 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Nucleoside diphosphate kinase A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 nucleoside diphosphate kinase A measurement http://www.ebi.ac.uk/efo/EFO_0009947 GCST90162468 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peroxisomal targeting signal 1 receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peroxisomal targeting signal 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0022001 GCST90162469 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proteasome activator complex subunit 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90162470 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein S100-A7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein S100-A7 measurement http://www.ebi.ac.uk/efo/EFO_0022002 GCST90162471 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. WNT1-inducible-signaling pathway protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 WNT1-inducible-signaling pathway protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0022003 GCST90162472 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ferritin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90162473 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90162474 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor ligand superfamily member 12 measurement http://www.ebi.ac.uk/efo/EFO_0010801 GCST90162475 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thrombopoietin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thrombopoietin measurement http://www.ebi.ac.uk/efo/EFO_0022004 GCST90162476 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Parathyroid hormone levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST90162477 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Somatostatin-28 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 somatostatin-28 measurement http://www.ebi.ac.uk/efo/EFO_0020745 GCST90162478 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dual specificity mitogen-activated protein kinase kinase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dual specificity mitogen-activated protein kinase kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0022005 GCST90162479 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cellular tumor antigen p53 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cellular tumor antigen p53 measurement http://www.ebi.ac.uk/efo/EFO_0022006 GCST90162480 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. PolyUbiquitin K48-linked levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 polyUbiquitin K48-linked measurement http://www.ebi.ac.uk/efo/EFO_0022007 GCST90162481 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. PolyUbiquitin K63-linked levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 polyUbiquitin K63-linked measurement http://www.ebi.ac.uk/efo/EFO_0022008 GCST90162482 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Netrin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 netrin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022009 GCST90162483 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leukocyte surface antigen CD47 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 leukocyte surface antigen CD47 measurement http://www.ebi.ac.uk/efo/EFO_0022010 GCST90162484 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ankyrin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 ankyrin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021874 GCST90162485 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 14-3-3 protein theta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 14-3-3 protein theta measurement http://www.ebi.ac.uk/efo/EFO_0022011 GCST90162486 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cysteine-rich with EGF-like domain protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 42 cysteine-rich with EGF-like domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021870 GCST90162487 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vesicular integral-membrane protein VIP36 measurement 2,935 Qatari ancestry individuals NA NR [10004359] 2 vesicular integral-membrane protein VIP36 measurement http://www.ebi.ac.uk/efo/EFO_0022012 GCST90162488 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibronectin Fragment 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fibronectin fragment 3 measurement http://www.ebi.ac.uk/efo/EFO_0008131 GCST90161782 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibronectin Fragment 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fibronectin fragment 4 measurement http://www.ebi.ac.uk/efo/EFO_0008132 GCST90161783 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Receptor-type tyrosine-protein kinase FLT3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 receptor-type tyrosine-protein kinase flt3 measurement http://www.ebi.ac.uk/efo/EFO_0020703 GCST90161784 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Follistatin-related protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 follistatin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020394 GCST90161785 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granzyme A levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90161786 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glycogen synthase kinase-3 alpha/beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glycogen synthase kinase-3 alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020412 GCST90161787 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Homeodomain-interacting protein kinase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 homeodomain-interacting protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020457 GCST90161788 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-15 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin 15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008172 GCST90161789 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. interleukin-18 receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90161790 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST90161791 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 insulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008160 GCST90161792 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallistatin levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90161793 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Lck levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90161795 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-synuclein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0009323 GCST90162496 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bone morphogenetic protein 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90162497 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Somatotropin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 somatotropin measurement http://www.ebi.ac.uk/efo/EFO_0022017 GCST90162498 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Extracellular superoxide dismutase [Cu-Zn] levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 extracellular superoxide dismutase [Cu-Zn] measurement http://www.ebi.ac.uk/efo/EFO_0022018 GCST90162499 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. R-spondin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 R-spondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0022019 GCST90162500 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin H levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90162501 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inhibin beta A chain:Inhibin beta B chain heterodimer levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 inhibin beta A chain:inhibin beta B chain heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020470 GCST90162502 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prostate-specific antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 prostate-specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0020660 GCST90162503 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor-binding protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90162504 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ribonuclease H1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ribonuclease H1 measurement http://www.ebi.ac.uk/efo/EFO_0022020 GCST90162505 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase transmembrane receptor ROR1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 tyrosine-protein kinase transmembrane receptor ROR1 measurement http://www.ebi.ac.uk/efo/EFO_0020831 GCST90162506 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chromogranin-A levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 chromogranin-A measurement http://www.ebi.ac.uk/efo/EFO_0022021 GCST90162507 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform measurement http://www.ebi.ac.uk/efo/EFO_0020637 GCST90161757 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. RAC-alpha/beta/gamma serine/threonine-protein kinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 RAC-alpha/beta/gamma serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021972 GCST90161758 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase PLK1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase PLK1 measurement http://www.ebi.ac.uk/efo/EFO_0020732 GCST90161759 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Renin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 renin measurement http://www.ebi.ac.uk/efo/EFO_0010616 GCST90161760 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein phosphatase non-receptor type 11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90161761 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stabilin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 stabilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020752 GCST90161762 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase TBK1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase TBK1 measurement http://www.ebi.ac.uk/efo/EFO_0020734 GCST90161763 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein phosphatase non-receptor type 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein phosphatase non-receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0020836 GCST90161764 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tryptase beta-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 21 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90161765 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tryptase gamma levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tryptase gamma measurement http://www.ebi.ac.uk/efo/EFO_0020792 GCST90161766 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin-fold modifier-conjugating enzyme 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ubiquitin-fold modifier-conjugating enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020843 GCST90161767 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apoptosis regulator Bcl-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 apoptosis regulator BCL-2 measurement http://www.ebi.ac.uk/efo/EFO_0020159 GCST90161768 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bcl-2-related protein A1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 BCL-2-related protein A1 measurement http://www.ebi.ac.uk/efo/EFO_0020178 GCST90161769 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytoplasmic tyrosine-protein kinase BMX levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cytoplasmic tyrosine-protein kinase BMX measurement http://www.ebi.ac.uk/efo/EFO_0020308 GCST90161770 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bone sialoprotein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bone sialoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020190 GCST90161771 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase BTK levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase BTK measurement http://www.ebi.ac.uk/efo/EFO_0020819 GCST90161772 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium/calmodulin-dependent protein kinase type 1D levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90161773 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium/calmodulin-dependent protein kinase type II subunit delta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calcium/calmodulin-dependent protein kinase type II subunit delta measurement http://www.ebi.ac.uk/efo/EFO_0020220 GCST90161774 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 13 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 carbonic anhydrase 13 measurement http://www.ebi.ac.uk/efo/EFO_0008067 GCST90161775 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90161776 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cyclin-dependent kinase 1:G2/mitotic-specific cyclin-B1 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cyclin-dependent kinase 1:g2/mitotic-specific cyclin-B1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020294 GCST90161777 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chymase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 chymase measurement http://www.ebi.ac.uk/efo/EFO_0020259 GCST90161778 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Casein kinase II subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 casein kinase II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020238 GCST90161779 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-A receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 ephrin type-A receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008123 GCST90161780 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-A receptor 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 ephrin type-a receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020352 GCST90161781 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ficolin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 ficolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008135 GCST90161707 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. GDNF family receptor alpha-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 gdnf family receptor alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020400 GCST90161708 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glypican-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glypican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020414 GCST90161709 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heparin cofactor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 heparin cofactor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008150 GCST90161710 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine protease HTRA2, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine protease HTRA2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020723 GCST90161711 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor-binding protein 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90161712 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-24 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-24 measurement http://www.ebi.ac.uk/efo/EFO_0020502 GCST90161713 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine-rich repeats and immunoglobulin-like domains protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 leucine-rich repeats and immunoglobulin-like domains protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020534 GCST90161714 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low-density lipoprotein receptor-related protein 8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 low-density lipoprotein receptor-related protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0020538 GCST90161715 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. T-lymphocyte surface antigen Ly-9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 T-lymphocyte surface antigen Ly-9 measurement http://www.ebi.ac.uk/efo/EFO_0008295 GCST90161716 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrilin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 matrilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020555 GCST90161717 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cell adhesion molecule 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0020251 GCST90161718 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Netrin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 netrin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020592 GCST90161719 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peptidoglycan recognition protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90161720 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. RGM domain family member B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 rgm domain family member b measurement http://www.ebi.ac.uk/efo/EFO_0020708 GCST90161721 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hemojuvelin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 hemojuvelin measurement http://www.ebi.ac.uk/efo/EFO_0008148 GCST90161722 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tissue factor pathway inhibitor levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90161723 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thrombospondin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90161724 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thrombospondin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 thrombospondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020771 GCST90161725 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase ABL1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase ABL1 measurement http://www.ebi.ac.uk/efo/EFO_0020818 GCST90161726 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Aminoacylase-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 aminoacylase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020141 GCST90161727 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Antithrombin-III levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 antithrombin-III measurement http://www.ebi.ac.uk/efo/EFO_0020155 GCST90161728 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Aurora kinase B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 aurora kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020169 GCST90161729 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. beta-adrenergic receptor kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 beta-adrenergic receptor kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020181 GCST90161730 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bone morphogenetic protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bone morphogenetic protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020184 GCST90161731 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium/calmodulin-dependent protein kinase type II subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calcium/calmodulin-dependent protein kinase type II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020218 GCST90161732 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium/calmodulin-dependent protein kinase type II subunit beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calcium/calmodulin-dependent protein kinase type II subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020219 GCST90161733 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 carbonic anhydrase 6 measurement http://www.ebi.ac.uk/efo/EFO_0008068 GCST90161734 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 carbonic anhydrase 7 measurement http://www.ebi.ac.uk/efo/EFO_0020231 GCST90161735 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cyclin-dependent kinase 2:Cyclin-A2 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cyclin-dependent kinase 2:cyclin-A2 complex measurement http://www.ebi.ac.uk/efo/EFO_0020295 GCST90161736 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cyclin-dependent kinase 5:Cyclin-dependent kinase 5 activator 1 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cyclin-dependent kinase 5:cyclin-dependent kinase 5 activator 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020296 GCST90161737 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cyclin-dependent kinase 8:Cyclin-C complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cyclin-dependent kinase 8:cyclin-c complex measurement http://www.ebi.ac.uk/efo/EFO_0020297 GCST90161738 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase Chk2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase CHK2 measurement http://www.ebi.ac.uk/efo/EFO_0020726 GCST90161739 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-type lectin domain family 4 member K levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-type lectin domain family 4 member K measurement http://www.ebi.ac.uk/efo/EFO_0020201 GCST90161740 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chordin-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 chordin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020257 GCST90161741 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase CSK levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase CSK measurement http://www.ebi.ac.uk/efo/EFO_0020820 GCST90161742 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin L2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cathepsin L2 measurement http://www.ebi.ac.uk/efo/EFO_0020244 GCST90161743 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dickkopf-related protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 Dickkopf-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008110 GCST90161744 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Extracellular matrix protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 14 extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008126 GCST90161745 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fetuin-B levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 fetuin-B measurement http://www.ebi.ac.uk/efo/EFO_0008128 GCST90161746 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granzyme H levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 granzyme h measurement http://www.ebi.ac.uk/efo/EFO_0020419 GCST90161747 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase HCK levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase HCK measurement http://www.ebi.ac.uk/efo/EFO_0020824 GCST90161748 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-17 receptor D levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin 17 receptor D measurement http://www.ebi.ac.uk/efo/EFO_0008177 GCST90161749 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 kallikrein-7 measurement http://www.ebi.ac.uk/efo/EFO_0008195 GCST90161750 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein kinase C iota type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein kinase c iota type measurement http://www.ebi.ac.uk/efo/EFO_0020681 GCST90161751 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Lyn, isoform B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase LYN, isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020828 GCST90161752 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase PAK 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 serine/threonine-protein kinase PAK 3 measurement http://www.ebi.ac.uk/efo/EFO_0020728 GCST90161753 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase PAK 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase PAK 7 measurement http://www.ebi.ac.uk/efo/EFO_0020730 GCST90161754 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plasma serine protease inhibitor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 plasma serine protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0020642 GCST90161755 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. PIK3CA/PIK3R1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 PIK3CA/PIK3R1 measurement http://www.ebi.ac.uk/efo/EFO_0021971 GCST90161756 Genome-wide sequencing 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Phenylalanine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90134464 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Proline levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90134465 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Serine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90134466 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Tryptophan levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90134467 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Tyrosine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90134468 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Urate levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90134469 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Carnitine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90134470 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Citrulline levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90134471 Genome-wide genotyping array 2022-09-20 35907915 Sun J 2022-07-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35907915 Multivariate genome-wide association study of depression, cognition, and memory phenotypes and validation analysis identify 12 cross-ethnic variants. Depression, cognition and memory (multivariate analysis) 278 Chinese ancestry dizygotic twins 355 cases, 1,775 controls Illumina [7399084] (imputed) 14 unipolar depression, memory performance, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004874, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90134646 Genome-wide genotyping array 2022-11-04 34930913 Dai H 2021-12-21 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34930913 Genome-wide association and functional interrogation identified a variant at 3p26.1 modulating ovarian cancer survival among Chinese women. Overall survival in ovarian cancer 1,346 Chinese ancestry individuals 784 Chinese ancestry individuals Illumina [6577217] (imputed) 2 overall survival, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0001075 GCST90102289 Genome-wide genotyping array 2022-09-13 36046430 Diamant N 2022-06-24 Cardiovasc Digit Health J www.ncbi.nlm.nih.gov/pubmed/36046430 Deep learning on resting electrocardiogram to identify impaired heart rate recovery. Predicted heart recovery rate 43,722 European ancestry individuals NA Affymetrix [NR] 8 heart rate response to recovery post exercise http://www.ebi.ac.uk/efo/EFO_0009185 GCST90134618 Genome-wide genotyping array 2022-09-14 35879402 Deak JD 2022-07-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35879402 Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci. Opioid use disorder 15,251 European ancestry cases, 538,935 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90134622 Genome-wide genotyping array 2022-09-14 35879402 Deak JD 2022-07-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35879402 Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci. Opioid use disorder 5,435 African ancestry cases, 79,442 African ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90134623 Genome-wide genotyping array 2022-09-14 35879402 Deak JD 2022-07-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35879402 Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci. Opioid use disorder 15,251 European ancestry cases, 538,935 European ancestry controls, 5,435 African ancestry cases, 79,442 African ancestry controls NA Affymetrix, Illumina [NR] (imputed) 2 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90134624 Genome-wide genotyping array 2022-09-14 35879402 Deak JD 2022-07-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35879402 Genome-wide association study in individuals of European and African ancestry and multi-trait analysis of opioid use disorder identifies 19 independent genome-wide significant risk loci. Opioid use disorder (MTAG) 15,251 European ancestry cases, 538,935 European ancestry controls, 5,435 African ancestry cases, 79,442 African ancestry controls NA Affymetrix, Illumina [NR] (imputed) 18 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90134625 Genome-wide genotyping array 2022-09-01 35769078 Liu T 2022-06-13 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35769078 A Genome-Wide Association Study of Prediabetes Status Change. Diabetes progression in prediabetes 354 White ancestry cases, 546 White ancestry controls 147 White ancestry cases, 3,676 White ancestry controls Affymetrix [10008913] (imputed) 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90134328 Genome-wide genotyping array 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. E3 ubiquitin-protein ligase CHIP levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 E3 ubiquitin-protein ligase CHIP measurement http://www.ebi.ac.uk/efo/EFO_0021904 GCST90161242 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CCAAT/enhancer-binding protein beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 CCAAT/enhancer-binding protein beta measurement http://www.ebi.ac.uk/efo/EFO_0021905 GCST90161243 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Gamma-enolase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 gamma-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021845 GCST90161244 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. E3 SUMO-protein ligase PIAS4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 E3 SUMO-protein ligase PIAS4 measurement http://www.ebi.ac.uk/efo/EFO_0021906 GCST90161245 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-10 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 interleukin-10 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0021890 GCST90161246 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Signal transducer and activator of transcription 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 signal transducer and activator of transcription 3 measurement http://www.ebi.ac.uk/efo/EFO_0021907 GCST90161247 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon regulatory factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon regulatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021908 GCST90161248 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transcription factor AP-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transcription factor AP-1 measurement http://www.ebi.ac.uk/efo/EFO_0021909 GCST90161249 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Induced myeloid leukemia cell differentiation protein Mcl-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 induced myeloid leukemia cell differentiation protein Mcl-1 measurement http://www.ebi.ac.uk/efo/EFO_0021910 GCST90161250 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 2'-5'-oligoadenylate synthase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 2'-5'-oligoadenylate synthase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021911 GCST90161251 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Myc proto-oncogene protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 myc proto-oncogene protein measurement http://www.ebi.ac.uk/efo/EFO_0021912 GCST90161252 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mothers against decapentaplegic homolog 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mothers against decapentaplegic homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0021913 GCST90161253 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mothers against decapentaplegic homolog 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mothers against decapentaplegic homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0021914 GCST90161254 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-23 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90161255 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet-derived growth factor receptor alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet-derived growth factor receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0021844 GCST90161256 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin 12 measurement http://www.ebi.ac.uk/efo/EFO_0004753 GCST90161257 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Signal transducer and activator of transcription 1-alpha/beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 signal transducer and activator of transcription 1-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0021915 GCST90161258 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Signal transducer and activator of transcription 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 signal transducer and activator of transcription 6 measurement http://www.ebi.ac.uk/efo/EFO_0021916 GCST90161259 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine-rich repeat serine/threonine-protein kinase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 leucine-rich repeat serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0021876 GCST90161260 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Osteocalcin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90161261 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin 5 measurement http://www.ebi.ac.uk/efo/EFO_0008185 GCST90161262 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 glycerol-3-phosphate dehydrogenase [NAD(+)]; cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0021917 GCST90161263 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Immunoglobulin A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serum immunoglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010127 GCST90161264 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 galectin-10 measurement http://www.ebi.ac.uk/efo/EFO_0021918 GCST90161265 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. HemK methyltransferase family member 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 hemK methyltransferase family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0021891 GCST90161266 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Killer cell immunoglobulin-like receptor 3DS1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 killer cell immunoglobulin-like receptor 3DS1 measurement http://www.ebi.ac.uk/efo/EFO_0020519 GCST90162291 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Killer cell lectin-like receptor subfamily F member 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 killer cell lectin-like receptor subfamily F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020520 GCST90162292 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lymphocyte activation gene 3 protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lymphocyte activation gene 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0020540 GCST90162293 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lysosome membrane protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lysosome membrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020545 GCST90162294 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. MHC class I polypeptide-related sequence B levels 2,935 Qatari ancestry individuals NA NR [10004359] 17 MHC class I polypeptide-related sequence B measurement http://www.ebi.ac.uk/efo/EFO_0008234 GCST90162295 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cell surface glycoprotein CD200 receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 cell surface glycoprotein CD200 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020253 GCST90162296 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Natural cytotoxicity triggering receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90162297 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Reticulon-4 receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90162298 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurogenic locus notch homolog protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90162299 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurogenic locus notch homolog protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 neurogenic locus notch homolog protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008246 GCST90162300 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurogenic locus notch homolog protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neurogenic locus notch homolog protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020600 GCST90162301 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neuronal cell adhesion molecule levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neuronal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020602 GCST90162302 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurexin-1-beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neurexin-1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020596 GCST90162303 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurexin-3-beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neurexin-3-beta measurement http://www.ebi.ac.uk/efo/EFO_0020597 GCST90162304 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. OX-2 membrane glycoprotein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 OX-2 membrane glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008253 GCST90162305 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prolactin receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 prolactin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020656 GCST90162306 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 19L levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90162307 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Roundabout homolog 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 roundabout homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0020713 GCST90162308 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Roundabout homolog 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 roundabout homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0020714 GCST90162309 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Semaphorin-6B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 semaphorin-6B measurement http://www.ebi.ac.uk/efo/EFO_0021885 GCST90162310 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Semaphorin-6A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90162311 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Intercellular adhesion molecule 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90162312 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sialic acid-binding Ig-like lectin 14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90162313 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SLAM family member 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 SLAM family member 6 measurement http://www.ebi.ac.uk/efo/EFO_0020742 GCST90162314 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Scavenger receptor class F member 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90162315 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neutrophil elastase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neutrophil elastase measurement http://www.ebi.ac.uk/efo/EFO_0020605 GCST90162366 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein E (isoform E2) levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 apolipoprotein E isoform E2 measurement http://www.ebi.ac.uk/efo/EFO_0008028 GCST90162367 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Troponin T; cardiac muscle levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90162368 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prothrombin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 prothrombin measurement http://www.ebi.ac.uk/efo/EFO_0020692 GCST90162369 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Epidermal growth factor receptor variant III levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90162370 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Annexin A6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 annexin A6 measurement http://www.ebi.ac.uk/efo/EFO_0020151 GCST90162371 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. T-lymphocyte activation antigen CD86 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 t-lymphocyte activation antigen CD86 measurement http://www.ebi.ac.uk/efo/EFO_0020762 GCST90162372 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein S100-A9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 protein s100-a9 measurement http://www.ebi.ac.uk/efo/EFO_0020687 GCST90162373 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Caspase-10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 caspase-10 measurement http://www.ebi.ac.uk/efo/EFO_0020239 GCST90162374 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carboxypeptidase E levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 carboxypeptidase e measurement http://www.ebi.ac.uk/efo/EFO_0020234 GCST90162375 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytoskeleton-associated protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytoskeleton-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020309 GCST90162376 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Copine-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 14 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90162377 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. G2/mitotic-specific cyclin-B1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 g2/mitotic-specific cyclin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020396 GCST90162378 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Junctional adhesion molecule C levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 junctional adhesion molecule C measurement http://www.ebi.ac.uk/efo/EFO_0020510 GCST90161581 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Limbic system-associated membrane protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 limbic system-associated membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0020537 GCST90161582 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mannose-binding protein C levels 2,935 Qatari ancestry individuals NA NR [10004359] 18 mannose-binding protein C measurement http://www.ebi.ac.uk/efo/EFO_0008224 GCST90161583 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Natural cytotoxicity triggering receptor 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 natural cytotoxicity triggering receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008243 GCST90161584 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Programmed cell death 1 ligand 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 programmed cell death 1 ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0008268 GCST90161585 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein phosphatase non-receptor type 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90161586 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sialic acid-binding Ig-like lectin 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 sialic acid-binding Ig-like lectin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008286 GCST90161587 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transforming growth factor beta receptor type 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transforming growth factor beta receptor type 3 measurement http://www.ebi.ac.uk/efo/EFO_0020779 GCST90161588 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thymic stromal lymphopoietin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thymic stromal lymphopoietin measurement http://www.ebi.ac.uk/efo/EFO_0020772 GCST90161589 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytotoxic T-lymphocyte protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytotoxic t-lymphocyte protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020312 GCST90161590 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-2-antiplasmin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 alpha-2-antiplasmin measurement http://www.ebi.ac.uk/efo/EFO_0020137 GCST90161591 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 fibroblast growth factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008129 GCST90161592 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. ICOS ligand levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90162266 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD226 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 CD226 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020246 GCST90162267 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Natural killer cell receptor 2B4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 natural killer cell receptor 2B4 measurement http://www.ebi.ac.uk/efo/EFO_0021882 GCST90162268 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD83 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 CD83 antigen measurement http://www.ebi.ac.uk/efo/EFO_0021983 GCST90162269 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CMRF35-like molecule 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90162270 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytotoxic and regulatory T-cell molecule levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytotoxic and regulatory t-cell molecule measurement http://www.ebi.ac.uk/efo/EFO_0020311 GCST90162271 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement decay-accelerating factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement decay-accelerating factor measurement http://www.ebi.ac.uk/efo/EFO_0008095 GCST90162272 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 6B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 6B measurement http://www.ebi.ac.uk/efo/EFO_0020815 GCST90162273 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-A receptor 10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin type-a receptor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020350 GCST90162274 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-B receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90162275 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-B receptor 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90162276 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transmembrane glycoprotein NMB levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90162277 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. X-linked interleukin-1 receptor accessory protein-like 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 x-linked interleukin-1 receptor accessory protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0020854 GCST90162278 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. interleukin-17 receptor B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin 17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0008176 GCST90162279 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-20 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-20 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020497 GCST90162280 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-22 receptor subunit alpha-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90162281 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-23 receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin 23 receptor measurement http://www.ebi.ac.uk/efo/EFO_0008181 GCST90162282 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-7 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin-7 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020508 GCST90162283 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leukocyte immunoglobulin-like receptor subfamily B member 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 17 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90162284 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leukocyte immunoglobulin-like receptor subfamily B member 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90162285 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein jagged-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein jagged-1 measurement http://www.ebi.ac.uk/efo/EFO_0008271 GCST90162286 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein jagged-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein jagged-2 measurement http://www.ebi.ac.uk/efo/EFO_0020675 GCST90162287 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Junctional adhesion molecule-like levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 junctional adhesion molecule-like measurement http://www.ebi.ac.uk/efo/EFO_0020511 GCST90162288 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Killer cell immunoglobulin-like receptor 2DL4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90162289 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Killer cell immunoglobulin-like receptor 3DL2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 killer cell immunoglobulin-like receptor 3DL2 measurement http://www.ebi.ac.uk/efo/EFO_0020518 GCST90162290 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 8 isoform A levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fibroblast growth factor 8 isoform A measurement http://www.ebi.ac.uk/efo/EFO_0020385 GCST90162061 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon lambda-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon lambda-1 measurement http://www.ebi.ac.uk/efo/EFO_0020485 GCST90162062 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon lambda-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon lambda-2 measurement http://www.ebi.ac.uk/efo/EFO_0020486 GCST90162063 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hepatocyte growth factor-like protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 48 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90162064 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Antileukoproteinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 antileukoproteinase measurement http://www.ebi.ac.uk/efo/EFO_0020154 GCST90162065 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pulmonary surfactant-associated protein D levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90162066 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Disintegrin and metalloproteinase domain-containing protein 12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 disintegrin and metalloproteinase domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0020328 GCST90162067 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bcl-2-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 BCL-2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020177 GCST90162068 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbohydrate sulfotransferase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 carbohydrate sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020225 GCST90162069 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbohydrate sulfotransferase 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 carbohydrate sulfotransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020226 GCST90162070 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Collectin-11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90162071 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 13 ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0020344 GCST90162072 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ectonucleoside triphosphate diphosphohydrolase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 ectonucleoside triphosphate diphosphohydrolase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020343 GCST90162073 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ectonucleoside triphosphate diphosphohydrolase 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 23 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90162074 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fc receptor-like protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 Fc receptor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008127 GCST90162075 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Gremlin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 gremlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020421 GCST90162076 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heterogeneous nuclear ribonucleoprotein A/B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heterogeneous nuclear ribonucleoprotein a/b measurement http://www.ebi.ac.uk/efo/EFO_0020441 GCST90162077 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine-rich repeat transmembrane neuronal protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 leucine-rich repeat transmembrane neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020531 GCST90162078 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine-rich repeat transmembrane neuronal protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 leucine-rich repeat transmembrane neuronal protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020532 GCST90162079 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lactadherin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 lactadherin measurement http://www.ebi.ac.uk/efo/EFO_0008203 GCST90162080 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proprotein convertase subtilisin/kexin type 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 28 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90162081 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Trypsin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 trypsin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008305 GCST90162262 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thymidylate synthase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thymidylate synthase measurement http://www.ebi.ac.uk/efo/EFO_0020774 GCST90162263 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor-inducible gene 6 protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tumor necrosis factor-inducible gene 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0008311 GCST90162264 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Programmed cell death 1 ligand 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90162265 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 13B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor ligand superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020793 GCST90161618 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement component C9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90161619 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin B levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90161620 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90161621 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90161622 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth/differentiation factor 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 growth/differentiation factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020430 GCST90161623 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Immunoglobulin M levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 immunoglobulin M measurement http://www.ebi.ac.uk/efo/EFO_0020466 GCST90161624 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin 2 measurement http://www.ebi.ac.uk/efo/EFO_0008331 GCST90161625 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-13 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin 13 measurement http://www.ebi.ac.uk/efo/EFO_0008171 GCST90161626 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-18-binding protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-18-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020495 GCST90161627 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lipopolysaccharide-binding protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 lipopolysaccharide-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0021894 GCST90161628 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coagulation factor Xa levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 coagulation factor XA measurement http://www.ebi.ac.uk/efo/EFO_0020266 GCST90161629 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Placenta growth factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 placenta growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010626 GCST90161630 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Retinoic acid receptor responder protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 retinoic acid receptor responder protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008274 GCST90161631 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NKG2D ligand 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 NKG2-D ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020609 GCST90161632 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NKG2D ligand 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 NKG2-D ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0020610 GCST90161633 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 27 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 27 measurement http://www.ebi.ac.uk/efo/EFO_0020812 GCST90161634 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Aurora kinase A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 aurora kinase A measurement http://www.ebi.ac.uk/efo/EFO_0020168 GCST90161635 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitogen-activated protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020574 GCST90161636 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Diablo homolog, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 diablo homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020323 GCST90161637 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vascular endothelial growth factor C levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 vascular endothelial growth factor C measurement http://www.ebi.ac.uk/efo/EFO_0020848 GCST90161638 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. T-cell surface glycoprotein CD4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 t-cell surface glycoprotein CD4 measurement http://www.ebi.ac.uk/efo/EFO_0020760 GCST90161639 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-2 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0010587 GCST90161640 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 1B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90161641 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Myeloid cell surface antigen CD33 levels 2,935 Qatari ancestry individuals NA NR [10004359] 16 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90161642 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dual specificity mitogen-activated protein kinase kinase 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 dual specificity mitogen-activated protein kinase kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0008113 GCST90162341 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitogen-activated protein kinase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020581 GCST90162342 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. AMP Kinase (alpha2beta2gamma1) levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 amp kinase (alpha2beta2gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020143 GCST90162343 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. cGMP-dependent 3',5'-cyclic phosphodiesterase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cGMP-specific 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0008081 GCST90162344 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peptidyl-prolyl cis-trans isomerase F, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peptidyl-prolyl cis-trans isomerase F, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020627 GCST90162345 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase 17B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 serine/threonine-protein kinase 17B measurement http://www.ebi.ac.uk/efo/EFO_0008281 GCST90162346 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inosine-5'-monophosphate dehydrogenase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 inosine-5'-monophosphate dehydrogenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008159 GCST90162347 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dual 3';5'-cyclic-AMP and -GMP phosphodiesterase 11A measurement http://www.ebi.ac.uk/efo/EFO_0021985 GCST90162348 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium/calmodulin-dependent 3';5'-cyclic nucleotide phosphodiesterase 1A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calcium/calmodulin-dependent 3';5'-cyclic nucleotide phosphodiesterase 1A measurement http://www.ebi.ac.uk/efo/EFO_0021986 GCST90162349 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. cGMP-inhibited 3',5'-cyclic phosphodiesterase A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cGMP-inhibited 3',5'-cyclic phosphodiesterase A measurement http://www.ebi.ac.uk/efo/EFO_0020255 GCST90162350 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. cAMP-specific 3',5'-cyclic phosphodiesterase 4D levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cAMP-specific 3',5'-cyclic phosphodiesterase 4D measurement http://www.ebi.ac.uk/efo/EFO_0020224 GCST90162351 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. cGMP-specific 3',5'-cyclic phosphodiesterase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cGMP-specific 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0008081 GCST90162352 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase kinase kinase 7:TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 fusion levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitogen-activated protein kinase kinase kinase 7:tgf-beta-activated kinase 1 and map3k7-binding protein 1 fusion measurement http://www.ebi.ac.uk/efo/EFO_0020582 GCST90162353 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Non-receptor tyrosine-protein kinase TYK2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 non-receptor tyrosine-protein kinase TYK2 measurement http://www.ebi.ac.uk/efo/EFO_0008251 GCST90162354 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Abelson tyrosine-protein kinase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 Abelson tyrosine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008012 GCST90162355 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Breast cancer anti-estrogen resistance protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 breast cancer anti-estrogen resistance protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008040 GCST90162356 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calreticulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calreticulin measurement http://www.ebi.ac.uk/efo/EFO_0020221 GCST90162357 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. GRB2-related adapter protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90162358 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrix metalloproteinase-16 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 matrix metalloproteinase-16 measurement http://www.ebi.ac.uk/efo/EFO_0020559 GCST90162359 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ras-related C3 botulinum toxin substrate 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ras-related C3 botulinum toxin substrate 3 measurement http://www.ebi.ac.uk/efo/EFO_0021987 GCST90162360 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SHC-transforming protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 shc-transforming protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020738 GCST90162361 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proto-oncogene vav levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proto-oncogene vav measurement http://www.ebi.ac.uk/efo/EFO_0021988 GCST90162362 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitochondrial glutamate carrier 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitochondrial glutamate carrier 2 measurement http://www.ebi.ac.uk/efo/EFO_0020572 GCST90162363 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Eotaxin levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90162364 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coagulation factor IXab levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 coagulation factor IXAB measurement http://www.ebi.ac.uk/efo/EFO_0020264 GCST90162365 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Scavenger receptor class F member 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90162316 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 19 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tumor necrosis factor receptor superfamily member 19 measurement http://www.ebi.ac.uk/efo/EFO_0020808 GCST90162317 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-27 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 interleukin 27 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008183 GCST90162318 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. TGF-beta receptor type-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tgf-beta receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020767 GCST90162319 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hepatitis A virus cellular receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90162320 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 12A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 12A measurement http://www.ebi.ac.uk/efo/EFO_0020802 GCST90162321 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Netrin receptor UNC5C levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 netrin receptor UNC5C measurement http://www.ebi.ac.uk/efo/EFO_0020590 GCST90162322 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Netrin receptor UNC5D levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90162323 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7a measurement http://www.ebi.ac.uk/efo/EFO_0020445 GCST90162324 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. AMP Kinase (alpha1beta1gamma1) levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 amp kinase (alpha1beta1gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020142 GCST90162325 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. GTPase KRas levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 GTPase kras measurement http://www.ebi.ac.uk/efo/EFO_0020432 GCST90162326 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glycylpeptide N-tetradecanoyltransferase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glycylpeptide n-tetradecanoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020413 GCST90162327 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 high affinity cgmp-specific 3',5'-cyclic phosphodiesterase 9a measurement http://www.ebi.ac.uk/efo/EFO_0020446 GCST90162328 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peptidyl-prolyl cis-trans isomerase D levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 peptidyl-prolyl cis-trans isomerase D measurement http://www.ebi.ac.uk/efo/EFO_0008256 GCST90162329 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proteasome activator complex subunit 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proteasome activator complex subunit 3 measurement http://www.ebi.ac.uk/efo/EFO_0020662 GCST90162330 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glucokinase regulatory protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 glucokinase regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0020406 GCST90162331 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Casein kinase II 2-alpha:2-beta heterotetramer levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 casein kinase II 2-alpha:2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020236 GCST90162332 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Casein kinase II 2-alpha':2-beta heterotetramer levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 casein kinase II 2-alpha':2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020237 GCST90162333 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 [pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1; mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0021984 GCST90162334 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kinesin-like protein KIF23 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 kinesin-like protein KIF23 measurement http://www.ebi.ac.uk/efo/EFO_0020522 GCST90162335 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inosine-5'-monophosphate dehydrogenase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 inosine-5'-monophosphate dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008158 GCST90162336 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 3-hydroxy-3-methylglutaryl-coenzyme A reductase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 3-hydroxy-3-methylglutaryl-coenzymeAreductase measurement http://www.ebi.ac.uk/efo/EFO_0020113 GCST90162337 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proprotein convertase subtilisin/kexin type 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90162338 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Nuclear receptor subfamily 1 group D member 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 nuclear receptor subfamily 1 group d member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020614 GCST90162339 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peptidyl-prolyl cis-trans isomerase E levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 peptidyl-prolyl cis-trans isomerase E measurement http://www.ebi.ac.uk/efo/EFO_0008257 GCST90162340 Genome-wide sequencing 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. N-linoleoyl ethanolamide levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 N-acylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0600028 GCST90026393 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. N-palmitoyl ethanolamide levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 N-acylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0600028 GCST90026394 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. N-vaccinoyl ethanolamide levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 N-acylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0600028 GCST90026395 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Total ethanolamine levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 N-acylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0600028 GCST90026396 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(22)S(19)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026397 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(23)S(20)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026398 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(24)DS(19)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026399 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(24)DS(20)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026400 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(24)S(16)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026401 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(24)S(19)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026402 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(24)S(20)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026403 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(25)S(20)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026404 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(26)S(19)] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026405 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Ceramide [N(24)S(19)] product-precursor ratio 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026406 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Total Ceramide [S19] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026407 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. Total Ceramide [S20] levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90026408 Genome-wide genotyping array 2022-11-24 33437986 McGurk KA 2021-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33437986 Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. N-docosahexaenoyl ethanolamide levels 999 European ancestry individuals NA Illumina [5280236] (imputed) 1 N-acylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0600028 GCST90026392 Genome-wide genotyping array 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin-conjugating enzyme E2 G2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 ubiquitin-conjugating enzyme E2 G2 measurement http://www.ebi.ac.uk/efo/EFO_0022035 GCST90162533 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transgelin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transgelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021884 GCST90162534 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. ATP synthase subunit O; mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ATP synthase subunit O; mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0022036 GCST90162535 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pro-opiomelanocortin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pro-opiomelanocortin measurement http://www.ebi.ac.uk/efo/EFO_0022037 GCST90162536 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Quinone oxidoreductase-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 quinone oxidoreductase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021880 GCST90162537 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pigment epithelium-derived factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 pigment epithelium-derived factor measurement http://www.ebi.ac.uk/efo/EFO_0021847 GCST90162538 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin F levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 cathepsin F measurement http://www.ebi.ac.uk/efo/EFO_0022038 GCST90162539 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Formimidoyltransferase-cyclodeaminase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 formimidoyltransferase-cyclodeaminase measurement http://www.ebi.ac.uk/efo/EFO_0021895 GCST90162540 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin carboxyl-terminal hydrolase 25 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 ubiquitin carboxyl-terminal hydrolase 25 measurement http://www.ebi.ac.uk/efo/EFO_0021881 GCST90162541 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plexin-B2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 plexin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0021867 GCST90162542 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Lyn levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase lyn measurement http://www.ebi.ac.uk/efo/EFO_0020827 GCST90161796 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Periostin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90161797 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet-derived growth factor receptor beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 21 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90161798 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Brevican core protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 brevican core protein measurement http://www.ebi.ac.uk/efo/EFO_0020193 GCST90161799 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. cAMP-dependent protein kinase catalytic subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cAMP-dependent protein kinase catalytic subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020222 GCST90161800 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ribosomal protein S6 kinase alpha-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ribosomal protein s6 kinase alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020709 GCST90161801 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. E-selectin levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90161802 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase 16 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 serine/threonine-protein kinase 16 measurement http://www.ebi.ac.uk/efo/EFO_0020724 GCST90161803 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Baculoviral IAP repeat-containing protein 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 baculoviral IAP repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020174 GCST90161804 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thrombopoietin Receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thrombopoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020769 GCST90161805 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thrombospondin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thrombospondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020770 GCST90161806 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. High affinity nerve growth factor receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 high affinity nerve growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020448 GCST90161807 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Trypsin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 trypsin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020791 GCST90161808 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dual specificity protein phosphatase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dual specificity protein phosphatase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020336 GCST90161809 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Xaa-Pro aminopeptidase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 xaa-pro aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020856 GCST90161810 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiotensinogen levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 angiotensinogen measurement http://www.ebi.ac.uk/efo/EFO_0008025 GCST90161811 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Beta-2-microglobulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 beta-2-microglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020180 GCST90161812 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020375 GCST90161813 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-X-C motif chemokine 13 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-X-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020205 GCST90161814 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Catalase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 catalase measurement http://www.ebi.ac.uk/efo/EFO_0008071 GCST90161815 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ciliary Neurotrophic Factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ciliary neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020260 GCST90161816 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 17 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 17 measurement http://www.ebi.ac.uk/efo/EFO_0020379 GCST90161817 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-X-C motif chemokine 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90161818 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon alpha-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020483 GCST90161819 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-17B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-17B measurement http://www.ebi.ac.uk/efo/EFO_0021973 GCST90161820 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Integrin alpha-I: beta-1 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 integrin alpha-I: beta-1 complex measurement http://www.ebi.ac.uk/efo/EFO_0008162 GCST90161821 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hepcidin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 hepcidin measurement http://www.ebi.ac.uk/efo/EFO_0020440 GCST90161822 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lymphotoxin alpha1:beta2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lymphotoxin alpha1:beta2 measurement http://www.ebi.ac.uk/efo/EFO_0020542 GCST90161823 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lymphotoxin alpha2:beta1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lymphotoxin alpha2:beta1 measurement http://www.ebi.ac.uk/efo/EFO_0020543 GCST90161824 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 22 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90161825 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 15 levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90161826 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Myeloblastin levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90161827 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stromal cell-derived factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 stromal cell-derived factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020756 GCST90161828 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carboxypeptidase B2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 carboxypeptidase B2 measurement http://www.ebi.ac.uk/efo/EFO_0008069 GCST90161829 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 17 levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 C-C motif chemokine 17 measurement http://www.ebi.ac.uk/efo/EFO_0008045 GCST90161830 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transforming growth factor beta-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transforming growth factor beta-3 measurement http://www.ebi.ac.uk/efo/EFO_0020782 GCST90161831 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thyroid stimulating hormone levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST90161832 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vasoactive Intestinal Peptide levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 vasoactive intestinal peptide measurement http://www.ebi.ac.uk/efo/EFO_0020849 GCST90161833 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD40 ligand levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST90161834 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dickkopf-related protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90161835 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stromelysin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 stromelysin‐2 measurement http://www.ebi.ac.uk/efo/EFO_0010621 GCST90162508 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. EGF-containing fibulin-like extracellular matrix protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 EGF-containing fibulin-like extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0022022 GCST90162509 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leptin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90162510 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kelch-like ECH-associated protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 kelch-like ECH-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0022023 GCST90162511 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Integrin alpha-IIb: beta-3 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 integrin alpha-IIb: beta-3 complex measurement http://www.ebi.ac.uk/efo/EFO_0020479 GCST90162512 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 26 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-C motif chemokine 26 measurement http://www.ebi.ac.uk/efo/EFO_0022024 GCST90162513 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Small ubiquitin-related modifier 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 small ubiquitin-related modifier 3 measurement http://www.ebi.ac.uk/efo/EFO_0022025 GCST90162514 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-17A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90162515 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cysteine and glycine-rich protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cysteine and glycine-rich protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0022027 GCST90162516 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neutrophil collagenase levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 neutrophil collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008248 GCST90162517 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phosphoglucomutase-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 phosphoglucomutase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021859 GCST90162518 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Down syndrome cell adhesion molecule levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 down syndrome cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0022028 GCST90162519 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mucin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90162520 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein FAM3B levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90162521 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neuregulin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neuregulin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022029 GCST90162522 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon gamma receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90162523 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low-density lipoprotein receptor-related protein 1; soluble levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 low-density lipoprotein receptor-related protein 1; soluble measurement http://www.ebi.ac.uk/efo/EFO_0022031 GCST90162524 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon alpha/beta receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 interferon alpha/beta receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021850 GCST90162525 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Trefoil factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 trefoil factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021865 GCST90162526 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Non-histone chromosomal protein HMG-14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 non-histone chromosomal protein HMG-14 measurement http://www.ebi.ac.uk/efo/EFO_0021872 GCST90162527 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-X-C motif chemokine 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-X-C motif chemokine 9 measurement http://www.ebi.ac.uk/efo/EFO_0022032 GCST90162528 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD63 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 CD63 antigen measurement http://www.ebi.ac.uk/efo/EFO_0022033 GCST90162529 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Trefoil factor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 trefoil factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0021846 GCST90162530 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 galectin-7 measurement http://www.ebi.ac.uk/efo/EFO_0022034 GCST90162531 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 galectin-9 measurement http://www.ebi.ac.uk/efo/EFO_0021863 GCST90162532 Genome-wide sequencing 2022-11-09 36333501 Ishigaki K 2022-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36333501 Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. Rheumatoid arthritis 22,350 European ancestry cases, 74,823 European ancestry controls, 11,025 East Asian ancestry cases, 162,608 East Asian ancestry controls, 999 African ancestry cases, 1,108 African ancestry controls, 986 South Asian ancestry cases, 1,258 South Asian ancestry controls, 511 Arab ancestry cases, 352 Arab ancestry controls NA Affymetrix, Illumina [20990826] (imputed) 145 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90132222 Genome-wide genotyping array 2022-11-09 36333501 Ishigaki K 2022-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36333501 Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. Rheumatoid arthritis 22,350 European ancestry cases, 74,823 European ancestry controls NA Affymetrix, Illumina [20990826] (imputed) 91 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90132223 Genome-wide genotyping array 2022-11-09 36333501 Ishigaki K 2022-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36333501 Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. Rheumatoid arthritis 11,025 East Asian ancestry cases, 162,608 East Asian ancestry controls NA Affymetrix, Illumina [20990826] (imputed) 42 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90132224 Genome-wide genotyping array 2022-11-09 36333501 Ishigaki K 2022-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36333501 Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive) 17,221 European ancestry cases, 74,823 European ancestry controls, 8,340 East Asian ancestry cases, 162,608 East Asian ancestry controls, 841 African ancestry cases, 1,108 African ancestry controls, 689 South Asian ancestry cases, 1,258 South Asian ancestry controls, 357 Arab ancestry cases, 352 Arab ancestry controls NA Affymetrix, Illumina [20990826] (imputed) 118 rheumatoid arthritis, anti-citrullinated protein antibody seropositivity, rheumatoid factor seropositivity measurement http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0007837, http://www.ebi.ac.uk/efo/EFO_0007791 GCST90132225 Genome-wide genotyping array 2022-11-09 36333501 Ishigaki K 2022-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36333501 Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive) 17,221 European ancestry cases, 74,823 European ancestry controls NA Affymetrix, Illumina [20990826] (imputed) 91 rheumatoid arthritis, anti-citrullinated protein antibody seropositivity, rheumatoid factor seropositivity measurement http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0007837, http://www.ebi.ac.uk/efo/EFO_0007791 GCST90132226 Genome-wide genotyping array 2022-11-09 36333501 Ishigaki K 2022-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36333501 Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis. Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive) 8,340 East Asian ancestry cases, 162,608 East Asian ancestry controls NA Affymetrix, Illumina [20990826] (imputed) 31 rheumatoid arthritis, anti-citrullinated protein antibody seropositivity, rheumatoid factor seropositivity measurement http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0007837, http://www.ebi.ac.uk/efo/EFO_0007791 GCST90132227 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. 1-aminocyclopropane-1-carboxylate levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 1-aminocyclopropane-1-carboxylic acid meaaurement http://www.ebi.ac.uk/efo/EFO_0021828 GCST90134439 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. 1-methylnicotinamide levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90134440 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. 3-methyl-2-oxindole levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 3-methyl-2-oxindole measurement http://www.ebi.ac.uk/efo/EFO_0021830 GCST90134441 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Bilirubin levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 3 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90134442 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Biliverdin levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 4 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90134443 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Caprylic acid levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 caprylic acid measurement http://www.ebi.ac.uk/efo/EFO_0021831 GCST90134444 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Creatine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90134445 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Creatinine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90134446 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. D-gulonic acid gama-lactone levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 L-Gulonic acid gamma-lactone measurement http://www.ebi.ac.uk/efo/EFO_0021832 GCST90134447 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Glycerate levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90134448 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Hypotaurine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90134449 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Hypoxanthine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90134450 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. L-arabitol levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 L-arabitol measurement http://www.ebi.ac.uk/efo/EFO_0021834 GCST90134451 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Melanin levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 melanin measurement http://www.ebi.ac.uk/efo/EFO_0021835 GCST90134452 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. N-acetyl-d-tryptophan levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 N-acetyl-d-tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021836 GCST90134453 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Palmitoleic acid levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 palmitoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0007973 GCST90134454 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Pyridoxamine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 pyridoxamine measurement http://www.ebi.ac.uk/efo/EFO_0021837 GCST90134455 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Pyruvate levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90134456 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Rac-glycerol 1-myristate levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 glycerol-1-myristate measurement http://www.ebi.ac.uk/efo/EFO_0021840 GCST90134457 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Sorbate levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 sorbate measurement http://www.ebi.ac.uk/efo/EFO_0021838 GCST90134458 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Trans-cinnamaldehyde levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 cinnamaldehyde measurement http://www.ebi.ac.uk/efo/EFO_0021839 GCST90134459 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Xanthine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 1 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90134460 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Glutamine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90134461 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Histidine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90134462 Genome-wide genotyping array 2022-09-20 35888748 Liu C 2022-07-06 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888748 Crosstalk between Host Genome and Metabolome among People with HIV in South Africa. Inosine levels 998 Sub-Saharan African ancestry individuals NA Illumina [NR] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90134463 Genome-wide genotyping array 2022-08-24 35661827 Praveen K 2022-06-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35661827 Population-scale analysis of common and rare genetic variation associated with hearing loss in adults. Hearing loss 125,749 European ancestry cases, 469,497 European ancestry controls NA Affymetrix, Illumina [15881489] (imputed) 53 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST90132906 Genome-wide genotyping array 2022-08-24 35661827 Praveen K 2022-06-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35661827 Population-scale analysis of common and rare genetic variation associated with hearing loss in adults. Hearing loss 125,749 European ancestry cases, 469,497 European ancestry controls NA Affymetrix, Illumina [2923124] (imputed) 33 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST90132907 Genome-wide genotyping array, Exome-wide sequencing 2022-07-07 35379174 Lim EB 2022-04-04 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35379174 Identification and functional validation of HLA-C as a potential gene involved in colorectal cancer in the Korean population. Colorectal cancer 194 Korean ancestry cases, 600 Korean ancestry controls NA Illumina [43082] 2 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90105079 Genome-wide genotyping array 2022-09-14 35879408 Shi G 2022-07-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35879408 Genome-wide variance quantitative trait locus analysis suggests small interaction effects in blood pressure traits. Systolic blood pressure 396,077 European ancestry individuals NA NR [9117915] (imputed) 8 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90134634 Genome-wide genotyping array 2022-09-14 35879408 Shi G 2022-07-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35879408 Genome-wide variance quantitative trait locus analysis suggests small interaction effects in blood pressure traits. Diastolic blood pressure 396,079 European ancestry individuals NA NR [9117915] (imputed) 5 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90134635 Genome-wide genotyping array 2022-09-14 35879408 Shi G 2022-07-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35879408 Genome-wide variance quantitative trait locus analysis suggests small interaction effects in blood pressure traits. Pulse pressure 396,077 European ancestry individuals NA NR [9117915] (imputed) 1 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90134636 Genome-wide genotyping array 2022-08-19 34329319 Streicher SA 2021-07-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/34329319 Genome-wide association study of pancreatic fat: The Multiethnic Cohort Adiposity Phenotype Study. Pancreas fat 144 African American individuals, 129 European ancestry individuals, 206 Japanese American individuals, 187 Latino individuals, 138 Native Hawaiian ancestry individuals NA Illumina [9542479] (imputed) 2 pancreas fat measurement http://www.ebi.ac.uk/efo/EFO_0600049 GCST90027067 Genome-wide genotyping array 2022-08-22 35910207 Zecevic M 2022-07-14 Front Genet www.ncbi.nlm.nih.gov/pubmed/35910207 Genome-Wide Association Study of COVID-19 Outcomes Reveals Novel Host Genetic Risk Loci in the Serbian Population. COVID-19 related pneumonia 128 European ancestry individuals NA Illumina [7496155] (imputed) 5 pneumonia, COVID-19 http://www.ebi.ac.uk/efo/EFO_0003106, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104347 Genome-wide genotyping array 2022-08-22 35910207 Zecevic M 2022-07-14 Front Genet www.ncbi.nlm.nih.gov/pubmed/35910207 Genome-Wide Association Study of COVID-19 Outcomes Reveals Novel Host Genetic Risk Loci in the Serbian Population. Severe COVID-19 disease 82 European ancestry individuals NA Illumina [6695505] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104348 Genome-wide genotyping array 2022-09-05 35762106 Weintraub D 2022-06-27 Ann Clin Transl Neurol www.ncbi.nlm.nih.gov/pubmed/35762106 Genetic prediction of impulse control disorders in Parkinson's disease. Impulse control disorders in Parkinson’s disease 1,976 European ancestry cases, 3,286 European ancestry controls NA Illumina [15200000] (imputed) 4 impulse control disorder http://purl.obolibrary.org/obo/MONDO_0001162 GCST90134329 Genome-wide genotyping array 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neuronal growth regulator 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 neuronal growth regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0021932 GCST90161292 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. B-cell lymphoma 6 protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 B-cell lymphoma 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0021933 GCST90161293 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Follistatin-related protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 follistatin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021934 GCST90161294 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Osteopontin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 osteopontin measurement http://www.ebi.ac.uk/efo/EFO_0021776 GCST90161295 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lumican levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lumican measurement http://www.ebi.ac.uk/efo/EFO_0021889 GCST90161296 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD177 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 17 cD177 antigen measurement http://www.ebi.ac.uk/efo/EFO_0021866 GCST90161297 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Choline/ethanolamine kinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 choline/ethanolamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0021935 GCST90161298 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SPARC-related modular calcium-binding protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 sPARC-related modular calcium-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021868 GCST90161299 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein Z-dependent protease inhibitor levels 2,935 Qatari ancestry individuals NA NR [10004359] 25 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90161300 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine-rich repeat transmembrane protein FLRT2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 leucine-rich repeat transmembrane protein FLRT2 measurement http://www.ebi.ac.uk/efo/EFO_0021860 GCST90161301 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leucine-rich repeat transmembrane protein FLRT3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90161302 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Immunoglobulin superfamily containing leucine-rich repeat protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 immunoglobulin superfamily containing leucine-rich repeat protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021879 GCST90161303 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vitronectin levels 2,935 Qatari ancestry individuals NA NR [10004359] 24 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90161304 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Desmocollin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 desmocollin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021936 GCST90161305 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low-density lipoprotein receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 low-density lipoprotein receptor measurement http://www.ebi.ac.uk/efo/EFO_0021937 GCST90161306 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hexokinase-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 hexokinase-2 measurement http://www.ebi.ac.uk/efo/EFO_0021938 GCST90161307 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hexokinase-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 hexokinase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021939 GCST90161308 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Semaphorin-5A levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 semaphorin-5A measurement http://www.ebi.ac.uk/efo/EFO_0021864 GCST90161309 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Latent-transforming growth factor beta-binding protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 latent-transforming growth factor beta-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021940 GCST90161310 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. PILR alpha-associated neural protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 PILR alpha-associated neural protein measurement http://www.ebi.ac.uk/efo/EFO_0021941 GCST90161311 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Adrenomedullin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 adrenomedullin measurement http://www.ebi.ac.uk/efo/EFO_0010909 GCST90161312 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein S100-A4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein S100-A4 measurement http://www.ebi.ac.uk/efo/EFO_0021893 GCST90161313 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. E3 ubiquitin-protein ligase RNF43 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 e3 ubiquitin-protein ligase RNF43 measurement http://www.ebi.ac.uk/efo/EFO_0021886 GCST90161314 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 10D levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 10D measurement http://www.ebi.ac.uk/efo/EFO_0021942 GCST90161315 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. E3 ubiquitin-protein ligase ZNRF3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 E3 ubiquitin-protein ligase ZNRF3 measurement http://www.ebi.ac.uk/efo/EFO_0021943 GCST90161316 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pyridoxal kinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pyridoxal kinase measurement http://www.ebi.ac.uk/efo/EFO_0021919 GCST90161267 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Toll-like receptor 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 toll-like receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0021920 GCST90161268 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Regenerating islet-derived protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 regenerating islet-derived protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021921 GCST90161269 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heat shock protein beta-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 heat shock protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0010595 GCST90161270 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chitinase-3-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 19 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90161271 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-enolase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 alpha-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021922 GCST90161272 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein L1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90161273 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021923 GCST90161274 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD59 glycoprotein levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 CD59 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0021924 GCST90161275 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fatty acid-binding protein, liver levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fatty acid-binding protein; liver measurement http://www.ebi.ac.uk/efo/EFO_0021925 GCST90161276 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth/differentiation factor 11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90161277 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Betacellulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 betacellulin measurement http://www.ebi.ac.uk/efo/EFO_0021883 GCST90161278 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hypoxia-inducible factor 1-alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 hypoxia-inducible factor 1-alpha measurement http://www.ebi.ac.uk/efo/EFO_0021926 GCST90161279 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein S100-A6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein S100-A6 measurement http://www.ebi.ac.uk/efo/EFO_0021927 GCST90161280 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Secreted and transmembrane protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 secreted and transmembrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021852 GCST90161281 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. R-spondin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 r-spondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0021878 GCST90161282 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lithostathine-1-alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90161283 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bcl-2-like protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bcl-2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021928 GCST90161284 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. vascular endothelial growth factor D levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90161285 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sclerostin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 sclerostin measurement http://www.ebi.ac.uk/efo/EFO_0010606 GCST90161286 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein FAM3D levels 2,935 Qatari ancestry individuals NA NR [10004359] 16 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90161287 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chorionic somatomammotropin hormone levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 chorionic somatomammotropin hormone measurement http://www.ebi.ac.uk/efo/EFO_0021929 GCST90161288 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin-B1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0021930 GCST90161289 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Synaptosomal-associated protein 25 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 synaptosomal-associated protein 25 measurement http://www.ebi.ac.uk/efo/EFO_0021858 GCST90161290 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ly6/PLAUR domain-containing protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 Ly6/PLAUR domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0021931 GCST90161291 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endoplasmic reticulum aminopeptidase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 14 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90162204 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. ATP synthase subunit beta, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ATP synthase subunit beta, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020166 GCST90162205 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement component 1 Q subcomponent-binding protein, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement component 1 q subcomponent-binding protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020280 GCST90162206 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage-capping protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 macrophage-capping protein measurement http://www.ebi.ac.uk/efo/EFO_0020549 GCST90162207 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 carbonic anhydrase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020227 GCST90162208 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 carbonic anhydrase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020228 GCST90162209 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin Z levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 cathepsin Z measurement http://www.ebi.ac.uk/efo/EFO_0008074 GCST90162210 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Baculoviral IAP repeat-containing protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 baculoviral IAP repeat-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020173 GCST90162211 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Adapter molecule crk levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 adapter molecule CRK measurement http://www.ebi.ac.uk/efo/EFO_0020128 GCST90162212 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Drebrin-like protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 drebrin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020333 GCST90162213 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dermatopontin levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90162214 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Desmocollin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 desmocollin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020320 GCST90162215 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Elafin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90162216 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endoplasmic reticulum resident protein 29 levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 endoplasmic reticulum resident protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0020346 GCST90162217 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. S-formylglutathione hydrolase levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 S-formylglutathione hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0008275 GCST90162218 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fatty acid-binding protein, epidermal levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fatty acid-binding protein, epidermal measurement http://www.ebi.ac.uk/efo/EFO_0020372 GCST90162219 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Focal adhesion kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 focal adhesion kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020393 GCST90162220 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Immunoglobulin alpha Fc receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 immunoglobulin alpha fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0020462 GCST90162221 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor receptor 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020391 GCST90162222 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibrinogen gamma chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibrinogen gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0020374 GCST90162223 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet glycoprotein Ib alpha chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 platelet glycoprotein ib alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0020645 GCST90162224 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glypican-5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 glypican-5 measurement http://www.ebi.ac.uk/efo/EFO_0008139 GCST90162225 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granulins levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90162226 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glutathione S-transferase A3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glutathione s-transferase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020409 GCST90162227 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heterogeneous nuclear ribonucleoprotein K levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heterogeneous nuclear ribonucleoprotein k measurement http://www.ebi.ac.uk/efo/EFO_0020442 GCST90162228 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C4b levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 complement C4b measurement http://www.ebi.ac.uk/efo/EFO_0008092 GCST90161342 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Coagulation Factor XI levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 factor XI measurement http://www.ebi.ac.uk/efo/EFO_0004694 GCST90161343 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 27 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 C-C motif chemokine 27 measurement http://www.ebi.ac.uk/efo/EFO_0020198 GCST90161344 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endostatin levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 endostatin measurement http://www.ebi.ac.uk/efo/EFO_0020347 GCST90161345 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Metalloproteinase inhibitor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 metalloproteinase inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020566 GCST90161346 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tissue-type plasminogen activator levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tissue-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0020776 GCST90161347 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prokineticin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 prokineticin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020655 GCST90161348 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Metalloproteinase inhibitor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 metalloproteinase inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020567 GCST90161349 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transforming growth factor beta-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transforming growth factor beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020780 GCST90161350 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vascular endothelial growth factor receptor 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90161351 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement C5 measurement http://www.ebi.ac.uk/efo/EFO_0020278 GCST90161352 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein E levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90161353 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Brain-derived neurotrophic factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST90161354 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement component C8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 complement component C8 measurement http://www.ebi.ac.uk/efo/EFO_0008094 GCST90161355 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin G levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cathepsin G measurement http://www.ebi.ac.uk/efo/EFO_0020242 GCST90161356 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-X-C motif chemokine 16 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90161357 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020376 GCST90161358 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 8 isoform B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 8 isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020386 GCST90161359 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Group IIE secretory phospholipase A2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 group IIe secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020424 GCST90161360 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium-dependent phospholipase A2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calcium-dependent phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020216 GCST90161361 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 20 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-C motif chemokine 20 measurement http://www.ebi.ac.uk/efo/EFO_0010910 GCST90161362 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serum amyloid P-component levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serum amyloid P-component measurement http://www.ebi.ac.uk/efo/EFO_0008283 GCST90161363 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mast/stem cell growth factor receptor Kit levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 mast/stem cell growth factor receptor kit measurement http://www.ebi.ac.uk/efo/EFO_0020554 GCST90161364 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Metalloproteinase inhibitor 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 metalloproteinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008231 GCST90161365 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiopoietin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 angiopoietin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020147 GCST90161366 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 1A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 1Ameasurement http://www.ebi.ac.uk/efo/EFO_0020809 GCST90161417 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. NT-3 growth factor receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 nt-3 growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020613 GCST90161418 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 17 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tumor necrosis factor receptor superfamily member 17 measurement http://www.ebi.ac.uk/efo/EFO_0020806 GCST90161419 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Decorin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 decorin measurement http://www.ebi.ac.uk/efo/EFO_0020315 GCST90161420 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calpain I levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calpain I measurement http://www.ebi.ac.uk/efo/EFO_0008064 GCST90161421 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Creatine kinase M-type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 creatine kinase m-type measurement http://www.ebi.ac.uk/efo/EFO_0020291 GCST90161422 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Epidermal growth factor receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90161423 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hepatocyte growth factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90161424 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 60 kDa heat shock protein, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 60 kda heat shock protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020121 GCST90161425 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C3b, inactivated levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 complement C3B, inactivated measurement http://www.ebi.ac.uk/efo/EFO_0020276 GCST90161426 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor-binding protein 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin-like growth factor-binding protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020477 GCST90161427 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor-binding protein 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 insulin-like growth factor-binding protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020478 GCST90161428 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. melanoma-derived growth regulatory protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90161429 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phospholipase A2, membrane associated levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90161430 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Oncostatin-M levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90161431 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet endothelial cell adhesion molecule levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90161432 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Persephin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 persephin measurement http://www.ebi.ac.uk/efo/EFO_0020632 GCST90161433 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet factor 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020644 GCST90161434 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vitamin K-dependent protein S levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 vitamin k-dependent protein S measurement http://www.ebi.ac.uk/efo/EFO_0020850 GCST90161435 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 13B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020803 GCST90161436 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 25 levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90161437 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thyroxine-Binding Globulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thyroxine-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0009172 GCST90161438 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 18 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tumor necrosis factor ligand superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020795 GCST90161439 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ciliary neurotrophic factor receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 ciliary neurotrophic factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020261 GCST90161440 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endothelial monocyte-activating polypeptide 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 endothelial monocyte-activating polypeptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020348 GCST90161441 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 15-hydroxyprostaglandin dehydrogenase [NAD(+)] levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 15-hydroxyprostaglandin dehydrogenase [NAD(+)] measurement http://www.ebi.ac.uk/efo/EFO_0020111 GCST90162229 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histidine-rich glycoprotein levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 histidine-rich glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008155 GCST90162230 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Eukaryotic initiation factor 4A-III levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 eukaryotic initiation factor 4a-III measurement http://www.ebi.ac.uk/efo/EFO_0020366 GCST90162231 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase JAK2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase JAK2 measurement http://www.ebi.ac.uk/efo/EFO_0020825 GCST90162232 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Galectin-3-binding protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 galectin-3-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010241 GCST90162233 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mammaglobin-B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mammaglobin-b measurement http://www.ebi.ac.uk/efo/EFO_0020552 GCST90162234 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrix metalloproteinase-14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 matrix metalloproteinase-14 measurement http://www.ebi.ac.uk/efo/EFO_0020558 GCST90162235 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 11 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitogen-activated protein kinase 11 measurement http://www.ebi.ac.uk/efo/EFO_0020575 GCST90162236 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 mitogen-activated protein kinase 12 measurement http://www.ebi.ac.uk/efo/EFO_0020576 GCST90162237 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 13 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitogen-activated protein kinase 13 measurement http://www.ebi.ac.uk/efo/EFO_0020577 GCST90162238 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitogen-activated protein kinase 14 measurement http://www.ebi.ac.uk/efo/EFO_0020578 GCST90162239 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Superoxide dismutase [Mn], mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 superoxide dismutase [Mn]; mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0021981 GCST90162240 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Moesin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 moesin measurement http://www.ebi.ac.uk/efo/EFO_0020583 GCST90162241 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Nicotinamide phosphoribosyltransferase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 nicotinamide phosphoribosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0020607 GCST90162242 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Adenylate kinase isoenzyme 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 adenylate kinase isoenzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020129 GCST90162243 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chloride intracellular channel protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 chloride intracellular channel protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020256 GCST90162244 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytoplasmic protein NCK1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytoplasmic protein NCK1 measurement http://www.ebi.ac.uk/efo/EFO_0020307 GCST90162245 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet-activating factor acetylhydrolase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet-activating factor acetylhydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020647 GCST90162246 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein deglycase DJ-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein deglycase DJ-1 measurement http://www.ebi.ac.uk/efo/EFO_0021982 GCST90162247 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peroxiredoxin-5, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peroxiredoxin-5, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020630 GCST90162248 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peroxiredoxin-6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peroxiredoxin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020631 GCST90162249 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin carboxyl-terminal hydrolase isozyme L1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ubiquitin carboxyl-terminal hydrolase isozyme L1 measurement http://www.ebi.ac.uk/efo/EFO_0020838 GCST90162250 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phosphoglycerate kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 phosphoglycerate kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020638 GCST90162251 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inorganic pyrophosphatase levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 inorganic pyrophosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008157 GCST90162252 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Adenylosuccinate lyase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 adenylosuccinate lyase measurement http://www.ebi.ac.uk/efo/EFO_0020130 GCST90162253 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cadherin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90161367 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. GDNF family receptor alpha-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 gdnf family receptor alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020401 GCST90161368 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin-B3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90161369 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. GDNF family receptor alpha-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 GDNF family receptor alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0008138 GCST90161370 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 21 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 C-C motif chemokine 21 measurement http://www.ebi.ac.uk/efo/EFO_0008048 GCST90161371 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. High mobility group protein B1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 high mobility group protein B1 measurement http://www.ebi.ac.uk/efo/EFO_0020449 GCST90161372 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 11B levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 tumor necrosis factor receptor superfamily member 11B measurement http://www.ebi.ac.uk/efo/EFO_0020801 GCST90161373 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Beta-endorphin levels 2,935 Qatari ancestry individuals NA NR [10004359] 13 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90161374 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement factor I levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 complement factor I measurement http://www.ebi.ac.uk/efo/EFO_0008099 GCST90161375 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Insulin-like growth factor-binding protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 IGFBP-3 measurement http://www.ebi.ac.uk/efo/EFO_0004626 GCST90161376 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C-C motif chemokine 2 measurement http://www.ebi.ac.uk/efo/EFO_0021961 GCST90161377 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Matrix metalloproteinase-9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 matrix metalloproteinase-9 measurement http://www.ebi.ac.uk/efo/EFO_0020561 GCST90161378 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Myeloperoxidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90161379 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prolactin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 prolactin measurement http://www.ebi.ac.uk/efo/EFO_0007003 GCST90161380 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vascular endothelial growth factor A levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90161381 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90161382 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor ligand superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0020798 GCST90161383 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiopoietin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90161384 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. T-lymphocyte activation antigen CD80 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 t-lymphocyte activation antigen CD80 measurement http://www.ebi.ac.uk/efo/EFO_0020761 GCST90161385 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0020816 GCST90161386 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytokine receptor-like factor 1:Cardiotrophin-like cytokine factor 1 Complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytokine receptor-like factor 1:cardiotrophin-like cytokine factor 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020305 GCST90161387 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cystatin-C levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90161388 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase receptor TYRO3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tyrosine-protein kinase receptor TYRO3 measurement http://www.ebi.ac.uk/efo/EFO_0020829 GCST90161389 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Eukaryotic translation initiation factor 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 eukaryotic translation initiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020369 GCST90161390 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin-A4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin-A4 measurement http://www.ebi.ac.uk/efo/EFO_0020356 GCST90161391 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet receptor Gi24 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 platelet receptor Gi24 measurement http://www.ebi.ac.uk/efo/EFO_0021877 GCST90161317 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin-A2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin-A2 measurement http://www.ebi.ac.uk/efo/EFO_0021944 GCST90161318 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein M levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 apolipoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0021945 GCST90161319 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytokine measurement http://www.ebi.ac.uk/efo/EFO_0004873 GCST90161320 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon alpha-10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon alpha-10 measurement http://www.ebi.ac.uk/efo/EFO_0021946 GCST90161321 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon alpha-7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon alpha-7 measurement http://www.ebi.ac.uk/efo/EFO_0021947 GCST90161322 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin-B2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90161323 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. HERV-H LTR-associating protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 HERV-H LTR-associating protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021948 GCST90161324 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 receptor type 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 interleukin 1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0008169 GCST90161325 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Amphoterin-induced protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 amphoterin-induced protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021949 GCST90161326 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Relaxin receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 relaxin receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021950 GCST90161327 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement component C1q receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90161328 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neuregulin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neuregulin-4 measurement http://www.ebi.ac.uk/efo/EFO_0021951 GCST90161329 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone H2B type 2-E levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone H2B type 2-E measurement http://www.ebi.ac.uk/efo/EFO_0021952 GCST90161330 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone H2A type 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone H2A type 3 measurement http://www.ebi.ac.uk/efo/EFO_0021953 GCST90161331 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone H3.1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone H3.1 measurement http://www.ebi.ac.uk/efo/EFO_0021954 GCST90161332 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon gamma levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90161333 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-36 beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-36 beta measurement http://www.ebi.ac.uk/efo/EFO_0021955 GCST90161334 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-36 alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin-36 alpha measurement http://www.ebi.ac.uk/efo/EFO_0021851 GCST90161335 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin-like protein ISG15 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 ubiquitin-like protein ISG15 measurement http://www.ebi.ac.uk/efo/EFO_0021875 GCST90161336 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin-A3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin-A3 measurement http://www.ebi.ac.uk/efo/EFO_0021956 GCST90161337 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 14-3-3 protein beta/alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 14-3-3 protein beta/alpha measurement http://www.ebi.ac.uk/efo/EFO_0021957 GCST90161338 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 14-3-3 protein epsilon levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 14-3-3 protein epsilon measurement http://www.ebi.ac.uk/efo/EFO_0021958 GCST90161339 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Annexin A5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 annexin A5 measurement http://www.ebi.ac.uk/efo/EFO_0021959 GCST90161340 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth/differentiation factor 8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 growth/differentiation factor 8 measurement http://www.ebi.ac.uk/efo/EFO_0021960 GCST90161341 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin-A5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin-A5 measurement http://www.ebi.ac.uk/efo/EFO_0020357 GCST90161392 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Receptor tyrosine-protein kinase erbB-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 receptor tyrosine-protein kinase erbb-2 measurement http://www.ebi.ac.uk/efo/EFO_0020700 GCST90161393 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Receptor tyrosine-protein kinase erbB-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 receptor tyrosine-protein kinase erbb-3 measurement http://www.ebi.ac.uk/efo/EFO_0020701 GCST90161394 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Receptor tyrosine-protein kinase erbB-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 receptor tyrosine-protein kinase erbb-4 measurement http://www.ebi.ac.uk/efo/EFO_0020702 GCST90161395 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor-associated calcium signal transducer 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor-associated calcium signal transducer 2 measurement http://www.ebi.ac.uk/efo/EFO_0020817 GCST90161396 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-6 receptor subunit beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin 6 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0008188 GCST90161397 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heme oxygenase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heme oxygenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020436 GCST90161398 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heat shock protein HSP 90-alpha/beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heat shock protein hsp 90-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020435 GCST90161399 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 Receptor accessory protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 interleukin 1 Receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008167 GCST90161400 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-10 receptor subunit beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 interleukin-10 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020489 GCST90161401 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-12 receptor subunit beta-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90161402 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-13 receptor subunit alpha-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 interleukin-13 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020493 GCST90161403 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cytokine receptor common subunit gamma levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cytokine receptor common subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0020304 GCST90161404 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Layilin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 layilin measurement http://www.ebi.ac.uk/efo/EFO_0020529 GCST90161405 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tumor necrosis factor receptor superfamily member 3 measurement http://www.ebi.ac.uk/efo/EFO_0020813 GCST90161406 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage mannose receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 macrophage mannose receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020548 GCST90161407 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage colony-stimulating factor 1 receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 macrophage colony-stimulating factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020547 GCST90161408 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage-stimulating protein receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 macrophage-stimulating protein receptor measurement http://www.ebi.ac.uk/efo/EFO_0020550 GCST90161409 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet-activating factor acetylhydrolase IB subunit beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet-activating factor acetylhydrolase ib subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020646 GCST90161410 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cadherin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cadherin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020213 GCST90161411 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein kinase C alpha type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein kinase c alpha type measurement http://www.ebi.ac.uk/efo/EFO_0020677 GCST90161412 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein kinase C zeta type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein kinase c zeta type measurement http://www.ebi.ac.uk/efo/EFO_0020683 GCST90161413 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Rab GDP dissociation inhibitor beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 rab gdp dissociation inhibitor beta measurement http://www.ebi.ac.uk/efo/EFO_0020697 GCST90161414 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Intercellular adhesion molecule 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 intercellular adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020482 GCST90161415 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Urokinase plasminogen activator surface receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90161416 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase pim-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase PIM-1 measurement http://www.ebi.ac.uk/efo/EFO_0020731 GCST90162389 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. RAC-beta serine/threonine-protein kinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 RAC-beta serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021989 GCST90162390 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Semaphorin-3E levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90162391 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein SET levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein set measurement http://www.ebi.ac.uk/efo/EFO_0020688 GCST90162392 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 13C levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tumor necrosis factor receptor superfamily member 13C measurement http://www.ebi.ac.uk/efo/EFO_0020804 GCST90162393 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transcription factor IIIB 90 kDa subunit levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transcription factor IIIb 90 kda subunit measurement http://www.ebi.ac.uk/efo/EFO_0020778 GCST90162394 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90162395 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leptin receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 18 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90162396 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 21 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 21 measurement http://www.ebi.ac.uk/efo/EFO_0020810 GCST90162397 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cadherin-15 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0020211 GCST90162398 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD27 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 CD27 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008078 GCST90162399 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 11A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 11A measurement http://www.ebi.ac.uk/efo/EFO_0020800 GCST90162400 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein phosphatase non-receptor type substrate 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 19 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90162401 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fatty acid-binding protein, heart levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fatty acid-binding protein, heart measurement http://www.ebi.ac.uk/efo/EFO_0020373 GCST90162402 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Troponin I, fast skeletal muscle levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 troponin i, fast skeletal muscle measurement http://www.ebi.ac.uk/efo/EFO_0020789 GCST90162403 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Troponin I, cardiac muscle levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 troponin i, cardiac muscle measurement http://www.ebi.ac.uk/efo/EFO_0020788 GCST90162404 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Atrial natriuretic factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 atrial natriuretic factor measurement http://www.ebi.ac.uk/efo/EFO_0004789 GCST90162405 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD166 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 CD166 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020245 GCST90162406 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Asialoglycoprotein receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 asialoglycoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020164 GCST90162407 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Beta-Ala-His dipeptidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 beta-Ala-His dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0008033 GCST90162408 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Collectin-12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90162409 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cystatin-SN levels 2,935 Qatari ancestry individuals NA NR [10004359] 7 cystatin-SN measurement http://www.ebi.ac.uk/efo/EFO_0008106 GCST90162410 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. ATP-dependent RNA helicase DDX19B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ATP-dependent rna helicase ddx19b measurement http://www.ebi.ac.uk/efo/EFO_0020167 GCST90162411 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ficolin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 ficolin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020392 GCST90162412 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth arrest-specific protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 growth arrest-specific protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020425 GCST90162413 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein 4.1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein 4.1 measurement http://www.ebi.ac.uk/efo/EFO_0020666 GCST90162135 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Estradiol 17-beta-dehydrogenase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 estradiol 17-beta-dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020365 GCST90162136 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Apolipoprotein D levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90162137 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020503 GCST90162138 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peptidyl-prolyl cis-trans isomerase B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peptidyl-prolyl cis-trans isomerase B measurement http://www.ebi.ac.uk/efo/EFO_0020626 GCST90162139 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein disulfide-isomerase A3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein disulfide-isomerase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020668 GCST90162140 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Trefoil factor 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90162141 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Afamin levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 afamin measurement http://www.ebi.ac.uk/efo/EFO_0008015 GCST90162142 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Olfactomedin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 olfactomedin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020617 GCST90162143 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Acid sphingomyelinase-like phosphodiesterase 3a levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90162144 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein FAM107B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein fam107b measurement http://www.ebi.ac.uk/efo/EFO_0020674 GCST90162145 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Gelsolin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 gelsolin measurement http://www.ebi.ac.uk/efo/EFO_0020402 GCST90162146 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Corticosteroid-binding globulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 corticosteroid-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0020288 GCST90162147 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. UMP-CMP kinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 UMP-CMP kinase measurement http://www.ebi.ac.uk/efo/EFO_0008313 GCST90162148 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lactoperoxidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 lactoperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0020525 GCST90162149 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Collagen alpha-1(VIII) chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 collagen alpha-1(VIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020269 GCST90162150 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inter-alpha-trypsin inhibitor heavy chain H4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 inter-alpha-trypsin inhibitor heavy chain h4 measurement http://www.ebi.ac.uk/efo/EFO_0020481 GCST90162151 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thioredoxin domain-containing protein 12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 33 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90162152 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 14-3-3 protein sigma levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 14-3-3 protein sigma measurement http://www.ebi.ac.uk/efo/EFO_0020110 GCST90162153 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. L-selectin levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90162154 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 10A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 10A measurement http://www.ebi.ac.uk/efo/EFO_0020799 GCST90162155 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-A receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin type-a receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020351 GCST90162156 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granulocyte colony-stimulating factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90162157 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glypican-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glypican-3 measurement http://www.ebi.ac.uk/efo/EFO_0020415 GCST90162158 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST90162159 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Growth factor receptor-bound protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 growth factor receptor-bound protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021990 GCST90162414 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heparan-sulfate 6-O-sulfotransferase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 heparan-sulfate 6-o-sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020437 GCST90162415 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heat shock protein HSP 90-beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heat shock protein HSP 90-beta measurement http://www.ebi.ac.uk/efo/EFO_0021991 GCST90162416 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-17 receptor C levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-17 receptor c measurement http://www.ebi.ac.uk/efo/EFO_0020494 GCST90162417 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mediator of RNA polymerase II transcription subunit 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90162418 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein kinase C beta type (splice variant beta-II) levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein kinase c beta type (splice variant beta-II) measurement http://www.ebi.ac.uk/efo/EFO_0020678 GCST90162419 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein kinase C gamma type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein kinase c gamma type measurement http://www.ebi.ac.uk/efo/EFO_0020680 GCST90162420 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glutamate carboxypeptidase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90162421 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 C-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008053 GCST90162422 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ras GTPase-activating protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 ras GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020698 GCST90162423 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Retinol-binding protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 retinol-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020707 GCST90162424 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Repulsive guidance molecule A levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 repulsive guidance molecule A measurement http://www.ebi.ac.uk/efo/EFO_0008273 GCST90162425 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 40S ribosomal protein S3a levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 40s ribosomal protein S3 measurement http://www.ebi.ac.uk/efo/EFO_0020117 GCST90162426 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Intercellular adhesion molecule 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90162427 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SLAM family member 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 13 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90162428 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proto-oncogene tyrosine-protein kinase Src levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proto-oncogene tyrosine-protein kinase Src measurement http://www.ebi.ac.uk/efo/EFO_0010927 GCST90162429 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stress-induced-phosphoprotein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 stress-induced-phosphoprotein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020755 GCST90162430 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Testican-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 testican-1 measurement http://www.ebi.ac.uk/efo/EFO_0020765 GCST90162431 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Testican-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 testican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020766 GCST90162432 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase WNK3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase WNK3 measurement http://www.ebi.ac.uk/efo/EFO_0021992 GCST90162433 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Small nuclear ribonucleoprotein F levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 small nuclear ribonucleoprotein F measurement http://www.ebi.ac.uk/efo/EFO_0008288 GCST90162434 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin D levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cathepsin D measurement http://www.ebi.ac.uk/efo/EFO_0010611 GCST90162435 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Epidermal growth factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90162436 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 18 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020807 GCST90162437 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fibroblast growth factor receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020388 GCST90162438 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Human Chorionic Gonadotropin levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90162185 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hemoglobin levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90162186 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Immunoglobulin D levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 immunoglobulin D measurement http://www.ebi.ac.uk/efo/EFO_0020463 GCST90162187 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Integrin alpha-V: beta-5 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 integrin alpha-V: beta-5 complex measurement http://www.ebi.ac.uk/efo/EFO_0020480 GCST90162188 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lysozyme C levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90162189 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 19 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-C motif chemokine 19 measurement http://www.ebi.ac.uk/efo/EFO_0008047 GCST90162190 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Muellerian-inhibiting factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 muellerian-inhibiting factor measurement http://www.ebi.ac.uk/efo/EFO_0020584 GCST90162191 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interstitial collagenase levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 interstitial collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008193 GCST90162192 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Collagenase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 collagenase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020271 GCST90162193 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sex hormone-binding globulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90162194 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Stanniocalcin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 stanniocalcin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020753 GCST90162195 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tissue factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tissue factor measurement http://www.ebi.ac.uk/efo/EFO_0010623 GCST90162196 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Epiregulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 epiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020361 GCST90162197 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 40S ribosomal protein SA levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 40s ribosomal protein SA measurement http://www.ebi.ac.uk/efo/EFO_0020119 GCST90162198 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Anterior gradient protein 2 homolog levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 anterior gradient protein 2 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020152 GCST90162199 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Delta-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90162379 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glypican-6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 glypican-6 measurement http://www.ebi.ac.uk/efo/EFO_0021871 GCST90162380 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heterogeneous nuclear ribonucleoproteins A2/B1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heterogeneous nuclear ribonucleoproteins A2/B1 measurement http://www.ebi.ac.uk/efo/EFO_0020444 GCST90162381 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0020805 GCST90162382 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-1 receptor antagonist protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90162383 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Keratin, type I cytoskeletal 18 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 keratin, type I cytoskeletal 18 measurement http://www.ebi.ac.uk/efo/EFO_0020517 GCST90162384 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor ligand superfamily member 14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90162385 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage Migration Inhibitory Factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST90162386 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neuroligin-4, X-linked levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 neuroligin-4, x-linked measurement http://www.ebi.ac.uk/efo/EFO_0020601 GCST90162387 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Osteomodulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 osteomodulin measurement http://www.ebi.ac.uk/efo/EFO_0020619 GCST90162388 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 1B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tumor necrosis factor receptor superfamily member 10B measurement http://www.ebi.ac.uk/efo/EFO_0021993 GCST90162439 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neuropilin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 neuropilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020603 GCST90162440 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. alpha-Fetoprotein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST90162441 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. BH3-interacting domain death agonist levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 BH3-interacting domain death agonist measurement http://www.ebi.ac.uk/efo/EFO_0021994 GCST90162442 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. beta-nerve growth factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST90162443 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement C3d fragment levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 complement C3D fragment measurement http://www.ebi.ac.uk/efo/EFO_0020277 GCST90162444 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. CD70 antigen levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 CD70 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020249 GCST90162445 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Teratocarcinoma-derived growth factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 23 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90162446 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Erythropoietin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 erythropoietin measurement http://www.ebi.ac.uk/efo/EFO_0020363 GCST90162447 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glial cell line-derived neurotrophic factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glial cell line-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0021887 GCST90162448 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interferon gamma receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interferon gamma receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020484 GCST90162449 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008192 GCST90162450 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Leukemia inhibitory factor receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90162451 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone-lysine N-methyltransferase EHMT2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 histone-lysine n-methyltransferase EHMT2 measurement http://www.ebi.ac.uk/efo/EFO_0020455 GCST90162452 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Noggin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 noggin measurement http://www.ebi.ac.uk/efo/EFO_0021995 GCST90162453 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein S100-A12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90162454 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Microtubule-associated protein tau levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 microtubule-associated protein tau measurement http://www.ebi.ac.uk/efo/EFO_0020570 GCST90162455 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 14-3-3 protein zeta/delta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 14-3-3 protein zeta/delta measurement http://www.ebi.ac.uk/efo/EFO_0021996 GCST90162456 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 3-hydroxyanthranilate 3,4-dioxygenase levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 3-hydroxyanthranilate 3;4-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0021997 GCST90162457 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fructose-bisphosphate aldolase A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fructose-bisphosphate aldolase measurement http://www.ebi.ac.uk/efo/EFO_0004809 GCST90162458 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Arginase-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 arginase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020160 GCST90162459 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bcl2-associated agonist of cell death levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bcl2-associated agonist of cell death measurement http://www.ebi.ac.uk/efo/EFO_0021998 GCST90162460 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dynactin subunit 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dynactin subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0020338 GCST90162461 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Elongation factor 1-beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 elongation factor 1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020345 GCST90162462 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Eukaryotic translation initiation factor 4H levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 eukaryotic translation initiation factor 4H measurement http://www.ebi.ac.uk/efo/EFO_0021999 GCST90162463 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lymphotactin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lymphotactin measurement http://www.ebi.ac.uk/efo/EFO_0008214 GCST90161986 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 13 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020195 GCST90161987 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurotrophin-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neurotrophin-3 measurement http://www.ebi.ac.uk/efo/EFO_0010791 GCST90161988 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neurotrophin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 neurotrophin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020604 GCST90161989 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pappalysin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pappalysin‐1 measurement http://www.ebi.ac.uk/efo/EFO_0010618 GCST90161990 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet-derived growth factor subunit B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet-derived growth factor subunit b measurement http://www.ebi.ac.uk/efo/EFO_0020650 GCST90161991 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plasmin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 plasmin measurement http://www.ebi.ac.uk/efo/EFO_0020643 GCST90161992 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plasminogen levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 plasma plasminogen measurement http://www.ebi.ac.uk/efo/EFO_0006309 GCST90161993 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Plasma kallikrein levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 plasma kallikrein measurement http://www.ebi.ac.uk/efo/EFO_0008260 GCST90161994 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. alpha-1-antichymotrypsin complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 alpha-1-antichymotrypsin complex measurement http://www.ebi.ac.uk/efo/EFO_0008018 GCST90161995 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. P-selectin levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90161996 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tenascin levels 2,935 Qatari ancestry individuals NA NR [10004359] 8 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90161997 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Transforming growth factor beta-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 transforming growth factor beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020781 GCST90161998 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thrombin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thrombin measurement http://www.ebi.ac.uk/efo/EFO_0020768 GCST90161999 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Urokinase-type plasminogen activator levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90162000 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement factor H levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90162001 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 72 kDa type IV collagenase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 72 kda type IV collagenase measurement http://www.ebi.ac.uk/efo/EFO_0020122 GCST90162002 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serotransferrin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 serotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020735 GCST90162003 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Histone H2A.z levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 histone H2A.Z measurement http://www.ebi.ac.uk/efo/EFO_0020454 GCST90162004 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thyroglobulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thyroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010050 GCST90162005 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 14-3-3 protein family levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 14-3-3 protein family measurement http://www.ebi.ac.uk/efo/EFO_0020109 GCST90162006 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Eukaryotic translation initiation factor 4E-binding protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 eukaryotic translation initiation factor 4E-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020368 GCST90162007 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 6-phosphogluconate dehydrogenase, decarboxylating levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 6-phosphogluconate dehydrogenase, decarboxylating measurement http://www.ebi.ac.uk/efo/EFO_0020120 GCST90162008 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Aflatoxin B1 aldehyde reductase member 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 aflatoxin B1 aldehyde reductase member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020132 GCST90162009 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alcohol dehydrogenase [NADP(+)] levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 alcohol dehydrogenase [NADP(+)] measurement http://www.ebi.ac.uk/efo/EFO_0021977 GCST90162010 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lymphocyte antigen 86 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lymphocyte antigen 86 measurement http://www.ebi.ac.uk/efo/EFO_0020541 GCST90161861 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine protease 27 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine protease 27 measurement http://www.ebi.ac.uk/efo/EFO_0008280 GCST90161862 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Membrane metallo-endopeptidase-like 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 membrane metallo-endopeptidase-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020564 GCST90161863 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dual specificity mitogen-activated protein kinase kinase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 17 dual specificity mitogen-activated protein kinase kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008112 GCST90161864 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase MRCK beta levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serine/threonine-protein kinase MRCK beta measurement http://www.ebi.ac.uk/efo/EFO_0020727 GCST90161865 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cell adhesion molecule 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cell adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020252 GCST90161866 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Nidogen-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90161867 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Opioid-binding protein/cell adhesion molecule levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 opioid-binding protein/cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020618 GCST90161868 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. OCIA domain-containing protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 OCIA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008252 GCST90161869 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Oxidized low-density lipoprotein receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 oxidized low-density lipoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020620 GCST90161870 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. alpha-2-macroglobulin receptor-associated protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 14 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90161871 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SLAM family member 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90161872 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. SLIT and NTRK-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 SLIT and NTRK-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021974 GCST90161873 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dickkopf-like protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 dickkopf-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020324 GCST90161874 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Tec levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase TEC measurement http://www.ebi.ac.uk/efo/EFO_0020830 GCST90161875 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Toll-like receptor 4:Lymphocyte antigen 96 complex levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90161876 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Vascular endothelial growth factor receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90161877 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. BMP-binding endothelial regulator protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 BMP-binding endothelial regulator protein measurement http://www.ebi.ac.uk/efo/EFO_0020183 GCST90161878 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cadherin-12 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cadherin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020210 GCST90161879 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcineurin subunit B type 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 calcineurin subunit B type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020215 GCST90161880 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement factor H-related protein 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90161881 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cation-independent mannose-6-phosphate receptor levels 2,935 Qatari ancestry individuals NA NR [10004359] 9 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90161882 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Kallikrein-14 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90161883 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage scavenger receptor types I and II levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90161884 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Membrane frizzled-related protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 membrane frizzled-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020563 GCST90161885 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Aromatic-L-amino-acid decarboxylase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 aromatic-l-amino-acid decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0020161 GCST90161836 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Adiponectin levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90161837 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-1-antitrypsin levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008327 GCST90161838 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-2-HS-glycoprotein levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90161839 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Arylsulfatase A levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90161840 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Basigin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 basigin measurement http://www.ebi.ac.uk/efo/EFO_0020176 GCST90161841 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bone morphogenetic protein 10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 bone morphogenetic protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020185 GCST90161842 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cadherin-6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cadherin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020214 GCST90161843 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium/calmodulin-dependent protein kinase type 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 15 calcium/calmodulin-dependent protein kinase type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008062 GCST90161844 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Caspase-3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 caspase-3 measurement http://www.ebi.ac.uk/efo/EFO_0008070 GCST90161845 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cathepsin E levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cathepsin E measurement http://www.ebi.ac.uk/efo/EFO_0020241 GCST90161846 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Chitotriosidase-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 13 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90161847 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Neural cell adhesion molecule L1-like protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 neural cell adhesion molecule l1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020595 GCST90161848 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-type lectin domain family 7 member A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-type lectin domain family 7 memberAmeasurement http://www.ebi.ac.uk/efo/EFO_0020203 GCST90161849 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mannan-binding lectin serine protease 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 5 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90161850 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Discoidin domain-containing receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 discoidin domain-containing receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020327 GCST90161851 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dickkopf-related protein 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90161852 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dipeptidyl peptidase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90161853 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endothelin-converting enzyme 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90161854 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-B receptor 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin type-b receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020354 GCST90161855 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ficolin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90161856 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. N-acetylglucosamine-6-sulfatase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90161857 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hepatocyte growth factor activator levels 2,935 Qatari ancestry individuals NA NR [10004359] 12 hepatocyte growth factor activator measurement http://www.ebi.ac.uk/efo/EFO_0008152 GCST90161858 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-22 receptor subunit alpha-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90161859 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Legumain levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 legumain measurement http://www.ebi.ac.uk/efo/EFO_0020530 GCST90161860 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Pyridoxal phosphate phosphatase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 pyridoxal phosphate phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0020694 GCST90161961 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 26S proteasome non-ATPase regulatory subunit 7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 26s proteasome non-atpase regulatory subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0020112 GCST90161962 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. S-phase kinase-associated protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 s-phase kinase-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020715 GCST90161963 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Sorting nexin-4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 sorting nexin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020747 GCST90161964 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin-conjugating enzyme E2 N levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ubiquitin-conjugating enzyme E2 N measurement http://www.ebi.ac.uk/efo/EFO_0020841 GCST90161965 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Epithelial discoidin domain-containing receptor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 epithelial discoidin domain-containing receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020362 GCST90161966 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020382 GCST90161967 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heat shock 70 kDa protein 1A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90161968 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Advanced glycosylation end product-specific receptor, soluble levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 advanced glycosylation end product-specific receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0020131 GCST90161969 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Bactericidal permeability-increasing protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 bactericidal permeability-increasing protein measurement http://www.ebi.ac.uk/efo/EFO_0020172 GCST90161970 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement component C6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 complement component C6 measurement http://www.ebi.ac.uk/efo/EFO_0020281 GCST90161971 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-C motif chemokine 24 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-C motif chemokine 24 measurement http://www.ebi.ac.uk/efo/EFO_0020197 GCST90161972 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Complement factor B levels 2,935 Qatari ancestry individuals NA NR [10004359] 4 complement factor B measurement http://www.ebi.ac.uk/efo/EFO_0008096 GCST90161973 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020383 GCST90161974 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibronectin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 fibronectin measurement http://www.ebi.ac.uk/efo/EFO_0008133 GCST90161975 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Follistatin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 follistatin measurement http://www.ebi.ac.uk/efo/EFO_0010614 GCST90161976 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Granzyme B levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 granzyme b measurement http://www.ebi.ac.uk/efo/EFO_0020418 GCST90161977 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Heparin-binding EGF-like growth factor levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 heparin-binding egf-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020438 GCST90161978 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Immunoglobulin E levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 immunoglobulin E measurement http://www.ebi.ac.uk/efo/EFO_0020464 GCST90161979 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-17D levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-17D measurement http://www.ebi.ac.uk/efo/EFO_0021976 GCST90161980 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-25 levels 2,935 Qatari ancestry individuals NA NR [10004359] 10 interleukin 25 measurement http://www.ebi.ac.uk/efo/EFO_0008182 GCST90161981 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-20 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin-20 measurement http://www.ebi.ac.uk/efo/EFO_0020496 GCST90161982 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-6 receptor subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 17 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90161983 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 interleukin 7 measurement http://www.ebi.ac.uk/efo/EFO_0008189 GCST90161984 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. C-X-C motif chemokine 10 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST90161985 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serum albumin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90161886 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alpha-2-macroglobulin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 alpha-2-macroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020138 GCST90161887 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Alanine aminotransferase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90161888 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiostatin levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 angiostatin measurement http://www.ebi.ac.uk/efo/EFO_0008024 GCST90161889 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Creatine kinase M-type:Creatine kinase B-type heterodimer levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 creatine kinase m-type:creatine kinase b-type heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020292 GCST90161890 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cyclin-dependent kinase inhibitor 1B levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 cyclin-dependent kinase inhibitor 1b measurement http://www.ebi.ac.uk/efo/EFO_0020298 GCST90161891 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Brain natriuretic peptide 32 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 brain natriuretic peptide 32 measurement http://www.ebi.ac.uk/efo/EFO_0020191 GCST90161892 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peptide YY levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peptide yy measurement http://www.ebi.ac.uk/efo/EFO_0020623 GCST90161893 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Secretin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 secretin measurement http://www.ebi.ac.uk/efo/EFO_0020719 GCST90161894 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tumor necrosis factor receptor superfamily member 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tumor necrosis factor receptor superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020814 GCST90161895 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Macrophage colony-stimulating factor 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 macrophage colony-stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020546 GCST90161896 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Activated Protein C levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 activated protein C measurement http://www.ebi.ac.uk/efo/EFO_0020126 GCST90161897 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Prostaglandin G/H synthase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 prostaglandin g/h synthase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020659 GCST90161898 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Syntaxin-1A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 syntaxin-1a measurement http://www.ebi.ac.uk/efo/EFO_0020759 GCST90161899 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiopoietin-1 receptor, soluble levels 2,935 Qatari ancestry individuals NA NR [10004359] 6 angiopoietin-1 receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008023 GCST90161900 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Disintegrin and metalloproteinase domain-containing protein 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 disintegrin and metalloproteinase domain-containing protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0020329 GCST90161901 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Angiopoietin-related protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 angiopoietin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020149 GCST90161902 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cadherin-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cadherin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020212 GCST90161903 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 9 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 carbonic anhydrase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020232 GCST90161904 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Carbonic anhydrase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 carbonic anhydrase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020229 GCST90161905 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Creatine kinase B-type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 creatine kinase b-type measurement http://www.ebi.ac.uk/efo/EFO_0020290 GCST90161906 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cystatin-S levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 cystatin-S measurement http://www.ebi.ac.uk/efo/EFO_0020300 GCST90161907 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Cystatin-D levels 2,935 Qatari ancestry individuals NA NR [10004359] 11 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90161908 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Endothelial cell-specific molecule 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 endothelial cell-specific molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010912 GCST90161909 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ephrin type-A receptor 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ephrin type-a receptor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020353 GCST90161910 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor 23 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90161911 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020389 GCST90161912 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Fibroblast growth factor receptor 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90161913 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Fgr levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 tyrosine-protein kinase FGR measurement http://www.ebi.ac.uk/efo/EFO_0020822 GCST90161914 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Tyrosine-protein kinase Fyn levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 tyrosine-protein kinase FYN measurement http://www.ebi.ac.uk/efo/EFO_0020823 GCST90161915 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Interleukin-12 receptor subunit beta-2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 interleukin-12 receptor subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020492 GCST90161916 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein kinase C theta type levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein kinase c theta type measurement http://www.ebi.ac.uk/efo/EFO_0020682 GCST90161917 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. MAP kinase-activated protein kinase 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 MAP kinase-activated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008225 GCST90161918 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. MAP kinase-activated protein kinase 5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 MAP kinase-activated protein kinase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020553 GCST90161919 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. MAP kinase-activated protein kinase 3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90161920 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Megakaryocyte-associated tyrosine-protein kinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 megakaryocyte-associated tyrosine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0020562 GCST90161921 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mitogen-activated protein kinase 8 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mitogen-activated protein kinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020580 GCST90161922 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Serine/threonine-protein kinase PAK 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 serine/threonine-protein kinase PAK 6 measurement http://www.ebi.ac.uk/efo/EFO_0020729 GCST90161923 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Platelet-derived growth factor C levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 platelet-derived growth factor c measurement http://www.ebi.ac.uk/efo/EFO_0020648 GCST90161924 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase pten measurement http://www.ebi.ac.uk/efo/EFO_0020635 GCST90161925 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Protein-tyrosine kinase 6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 protein-tyrosine kinase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020691 GCST90161926 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Toll-like receptor 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 toll-like receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020777 GCST90161927 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin-fold modifier 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ubiquitin-fold modifier 1 measurement http://www.ebi.ac.uk/efo/EFO_0020842 GCST90161928 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. AH receptor-interacting protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 AH receptor-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0020134 GCST90161929 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peptidyl-prolyl cis-trans isomerase A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peptidyl-prolyl cis-trans isomerase A measurement http://www.ebi.ac.uk/efo/EFO_0020625 GCST90161930 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dynein light chain roadblock-type 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 3 dynein light chain roadblock-type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008114 GCST90161931 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Persulfide dioxygenase ETHE1, mitochondrial levels 2,935 Qatari ancestry individuals NA NR [10004359] 2 persulfide dioxygenase ETHE1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008258 GCST90161932 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Glyceraldehyde-3-phosphate dehydrogenase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 glyceraldehyde-3-phosphate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0020411 GCST90161933 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. DnaJ homolog subfamily B member 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 DNAj homolog subfamily b member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020332 GCST90161934 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Malate dehydrogenase, cytoplasmic levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 malate dehydrogenase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020551 GCST90161935 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Nascent polypeptide-associated complex subunit alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 nascent polypeptide-associated complex subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020587 GCST90161936 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Peroxiredoxin-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 peroxiredoxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020629 GCST90161937 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Low molecular weight phosphotyrosine protein phosphatase levels 2,935 Qatari ancestry individuals NA NR [10004359] 20 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90161938 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proteasome subunit alpha type-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proteasome subunit alpha type-1 measurement http://www.ebi.ac.uk/efo/EFO_0020663 GCST90161939 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Proteasome subunit alpha type-6 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 proteasome subunit alpha type-6 measurement http://www.ebi.ac.uk/efo/EFO_0020665 GCST90161940 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. 40S ribosomal protein S7 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 40s ribosomal protein S7 measurement http://www.ebi.ac.uk/efo/EFO_0020118 GCST90161941 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ribosomal protein S6 kinase alpha-5 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ribosomal protein s6 kinase alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0020710 GCST90161942 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ribosome maturation protein SBDS levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ribosome maturation protein sbds measurement http://www.ebi.ac.uk/efo/EFO_0020711 GCST90161943 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Seizure 6-like protein 2 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 seizure 6-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020720 GCST90161944 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Small glutamine-rich tetratricopeptide repeat-containing protein alpha levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 small glutamine-rich tetratricopeptide repeat-containing protein alpha measurement http://www.ebi.ac.uk/efo/EFO_0020744 GCST90161945 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Translationally-controlled tumor protein levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 translationally-controlled tumor protein measurement http://www.ebi.ac.uk/efo/EFO_0020784 GCST90161946 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Thyroid peroxidase levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 thyroid peroxidase measurement http://www.ebi.ac.uk/efo/EFO_0020775 GCST90161947 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Ubiquitin-conjugating enzyme E2 L3 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 ubiquitin-conjugating enzyme E2 L3 measurement http://www.ebi.ac.uk/efo/EFO_0020840 GCST90161948 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. AT-rich interactive domain-containing protein 3A levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 AT-rich interactive domain-containing protein 3A measurement http://www.ebi.ac.uk/efo/EFO_0020165 GCST90161949 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Calcium/calmodulin-dependent protein kinase kinase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 calcium/calmodulin-dependent protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020217 GCST90161950 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Hsp90 co-chaperone Cdc37 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 hsp90 co-chaperone CDC37 measurement http://www.ebi.ac.uk/efo/EFO_0020458 GCST90161951 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Dynein light chain 1, cytoplasmic levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 dynein light chain 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020339 GCST90161952 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Importin subunit beta-1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 importin subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020468 GCST90161953 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Inhibitor of growth protein 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 inhibitor of growth protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020471 GCST90161954 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Lamin-B1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 lamin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020527 GCST90161955 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. L-lactate dehydrogenase B chain levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 L-lactate dehydrogenase B chain measurement http://www.ebi.ac.uk/efo/EFO_0020524 GCST90161956 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Methyl-CpG-binding domain protein 4 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 methyl-cpg-binding domain protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020569 GCST90161957 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Mesothelin levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 mesothelin measurement http://www.ebi.ac.uk/efo/EFO_0020565 GCST90161958 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. N-acetyl-D-glucosamine kinase levels 2,935 Qatari ancestry individuals NA NR [10004359] 1 N-acetyl-D-glucosamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0008239 GCST90161959 Genome-wide sequencing 2022-10-24 36168886 Thareja G 2022-09-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36168886 Differences and commonalities in the genetic architecture of protein quantitative trait loci in European and Arab populations. Phosphoglycerate mutase 1 levels 2,935 Qatari ancestry individuals NA NR [10004359] 0 phosphoglycerate mutase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020639 GCST90161960 Genome-wide sequencing 2022-08-18 35621206 Shi M 2022-05-27 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/35621206 Genetic Architecture of Plasma Alpha-Aminoadipic Acid Reveals a Relationship With High-Density Lipoprotein Cholesterol. alpha-Aminoadipic acid levels 2,580 European ancestry individuals, 2,190 African American individuals, 508 Chinese ancestry individuals, 64 Asian American ancestry individuals, 112 Native American, mixed or unknown ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 25 aminoadipic acid measurement http://www.ebi.ac.uk/efo/EFO_0010459 GCST90132306 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Common executive function 427,037 European ancestry individuals NA Affymetrix [7391068] (imputed) 129 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90162547 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Common executive function 93,024 European ancestry individuals NA Affymetrix [NR] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90162548 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Common executive function 256,135 European ancestry individuals NA Affymetrix [NR] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90162549 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Intelligence 216,381 European ancestry individuals NA Affymetrix [NR] (imputed) 17 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST90179114 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Reaction time 432,297 European ancestry individuals NA Affymetrix [NR] (imputed) 0 reaction time measurement http://www.ebi.ac.uk/efo/EFO_0008393 GCST90179115 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Prospective memory task 162,335 European ancestry individuals NA Affymetrix [NR] (imputed) 0 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90179116 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Pairs matching task 81,701 European ancestry individuals NA Affymetrix [NR] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90179117 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Trail making task-B 93,024 European ancestry individuals NA Affymetrix [NR] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90179118 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Symbol digit substitution task 84,125 European ancestry individuals NA Affymetrix [NR] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90179119 Genome-wide genotyping array 2022-10-26 36150907 Hatoum AS 2022-07-14 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36150907 Genome-wide Association Study Shows That Executive Functioning Is Influenced by GABAergic Processes and Is a Neurocognitive Genetic Correlate of Psychiatric Disorders. Digit span task 81,701 European ancestry individuals NA Affymetrix [NR] (imputed) 0 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST90179120 Genome-wide genotyping array 2022-11-08 36277789 Sethi A 2022-10-06 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/36277789 Calcification of the abdominal aorta is an under-appreciated cardiovascular disease risk factor in the general population. Abdominal aortic calcification levels 31,786 White British ancestry individuals 41,203 European ancestry individuals Affymetrix [9390169] (imputed) 4 abdominal aortic artery calcification http://www.ebi.ac.uk/efo/EFO_0004859 GCST90134614 Genome-wide genotyping array 2022-09-08 35886043 Armstrong ND 2022-07-15 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35886043 Genetic Contributors of Efficacy and Adverse Metabolic Effects of Chlorthalidone in African Americans from the Genetics of Hypertension Associated Treatments (GenHAT) Study. Diastolic blood pressure response to chlorthalidone in hypertension 3,982 African American individuals 570 African American individuals Illumina [20400000] (imputed) 0 response to diuretic, diastolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0006945 GCST90134552 Genome-wide genotyping array 2022-09-08 35886043 Armstrong ND 2022-07-15 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35886043 Genetic Contributors of Efficacy and Adverse Metabolic Effects of Chlorthalidone in African Americans from the Genetics of Hypertension Associated Treatments (GenHAT) Study. Systolic blood pressure response to chlorthalidone in hypertension 3,982 African American individuals 570 African American individuals Illumina [20400000] (imputed) 0 response to diuretic, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0006944 GCST90134551 Genome-wide genotyping array 2022-09-08 35886043 Armstrong ND 2022-07-15 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35886043 Genetic Contributors of Efficacy and Adverse Metabolic Effects of Chlorthalidone in African Americans from the Genetics of Hypertension Associated Treatments (GenHAT) Study. Fasting glucose response to chlorthalidone in hypertension 1,127 African American individuals 570 African American individuals Illumina [20400000] (imputed) 0 response to diuretic, fasting blood glucose change measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0010120 GCST90134553 Genome-wide genotyping array 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihomo-linolenoylcarnitine (C20:3n3 or 6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 dihomo-linolenoylcarnitine (C20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800547 GCST90140121 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosahexaenoylcarnitine (C22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 docosahexaenoylcarnitine (C22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800548 GCST90140122 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nervonoylcarnitine (C24:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 nervonoylcarnitine (C24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800549 GCST90140123 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosapentaenoylcarnitine (C22:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 docosapentaenoylcarnitine (C22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800550 GCST90140124 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycosyl ceramide (d18:1/20:0, d16:1/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 glycosyl ceramide (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800551 GCST90140125 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cortolone glucuronide (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90140126 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphatidylcholine (O-18:1/20:4, O-16:0/22:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 phosphatidylcholine (O-18:1/20:4, O-16:0/22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800553 GCST90140127 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-pentadecanoyl-GPC (16:0/15:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoyl-2-pentadecanoyl-GPC (16:0/15:0) measurement http://www.ebi.ac.uk/efo/EFO_0800554 GCST90140128 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-dodecenoylcarnitine (C12:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90140129 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-butenoylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-butenoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800556 GCST90140130 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hydroxy-cmpf levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 hydroxy-CMPF measurement http://www.ebi.ac.uk/efo/EFO_0800557 GCST90140131 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyarachidate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxyarachidate measurement http://www.ebi.ac.uk/efo/EFO_0800558 GCST90140132 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-stearoylserine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-stearoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800559 GCST90140133 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyoleate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxyoleate measurement http://www.ebi.ac.uk/efo/EFO_0800560 GCST90140134 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dodecenedioate (C12:1-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 dodecenedioate (C12:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800561 GCST90140135 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hexadecenedioate (C16:1-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90140136 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Octadecenedioate (C18:1-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 octadecenedioate (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800563 GCST90140137 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Heptenedioate (C7:1-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 heptenedioate (C7:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800564 GCST90140138 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Octadecadienedioate (C18:2-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 octadecadienedioate (C18:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800565 GCST90140139 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) measurement http://www.ebi.ac.uk/efo/EFO_0800566 GCST90140140 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-2-aminooctanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90140141 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxybutyroylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxybutyroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800568 GCST90140142 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glyco-beta-muricholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glyco-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800569 GCST90140143 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d17:1/14:0, d16:1/15:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140144 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tetradecadienoate (14:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tetradecadienoate (14:2) measurement http://www.ebi.ac.uk/efo/EFO_0800570 GCST90140145 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxysebacate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800571 GCST90140146 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dodecadienoate (12:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 dodecadienoate (12:2) measurement http://www.ebi.ac.uk/efo/EFO_0800572 GCST90140147 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 11beta-hydroxyandrosterone glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90140148 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cholic acid glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 cholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800574 GCST90140149 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Deoxycholic acid glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90140150 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-methylhexanoylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-methylhexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800576 GCST90140151 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-nonadecenoyl-GPC (19:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-nonadecenoyl-GPC (19:1) measurement http://www.ebi.ac.uk/efo/EFO_0800577 GCST90140152 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycoursodeoxycholic acid sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycoursodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800578 GCST90140153 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lithocholate sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 lithocholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800579 GCST90140154 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyhexanoylcarnitine (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxyhexanoylcarnitine (1) measurement http://www.ebi.ac.uk/efo/EFO_0800580 GCST90140155 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyhexanoylcarnitine (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxyhexanoylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800581 GCST90140156 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tetrahydrocortisol sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tetrahydrocortisol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800582 GCST90140157 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800583 GCST90140158 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurochenodeoxycholic acid 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 taurochenodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800584 GCST90140159 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tetradecadienedioate (C14:2-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 tetradecadienedioate (C14:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800585 GCST90140160 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pregnenetriol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 pregnenetriol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800586 GCST90140161 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pregnenetriol disulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90140162 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Undecenoylcarnitine (C11:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90140163 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-decenoylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3-decenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800589 GCST90140164 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxydecanoylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxydecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800590 GCST90140165 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800591 GCST90140166 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Picolinoylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90140167 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Branched chain 14:0 dicarboxylic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 branched chain 14:0 dicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0800593 GCST90140168 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (2 or 3)-decenoate (10:1n7 or n8) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 (2 or 3)-decenoate (10:1n7 or n8) measurement http://www.ebi.ac.uk/efo/EFO_0800594 GCST90140169 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isoursodeoxycholate sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 isoursodeoxycholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800595 GCST90140170 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ceramide (d18:2/24:1, d18:1/24:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90140096 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycosyl ceramide (d18:2/24:1, d18:1/24:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glycosyl ceramide (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0800532 GCST90140097 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800533 GCST90140098 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ceramide (d18:1/20:0, d16:1/22:0, d20:1/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90140099 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Stearoylcholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 stearoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800534 GCST90140100 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoylcholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 linoleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800535 GCST90140101 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nisinate (24:6n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 nisinate (24:6n3) measurement http://www.ebi.ac.uk/efo/EFO_0800536 GCST90140102 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:0/20:0, d16:0/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140103 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/19:0, d19:1/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140104 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140105 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/24:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140106 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/21:0, d16:2/23:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140107 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/23:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140108 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140109 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d17:2/16:0, d18:2/15:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90140110 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Heneicosapentaenoate (21:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 heneicosapentaenoate (21:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800537 GCST90140111 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linolenoylcarnitine (C18:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 linolenoylcarnitine (C18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800538 GCST90140112 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Behenoylcarnitine (C22) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 behenoylcarnitine (C22) measurement http://www.ebi.ac.uk/efo/EFO_0800539 GCST90140113 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arachidoylcarnitine (C20) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 arachidoylcarnitine (C20) measurement http://www.ebi.ac.uk/efo/EFO_0800540 GCST90140114 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lignoceroylcarnitine (C24) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 lignoceroylcarnitine (C24) measurement http://www.ebi.ac.uk/efo/EFO_0800541 GCST90140115 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cerotoylcarnitine (C26) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 8 cerotoylcarnitine (C26) measurement http://www.ebi.ac.uk/efo/EFO_0800542 GCST90140116 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ximenoylcarnitine (C26:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 8 ximenoylcarnitine (C26:1) measurement http://www.ebi.ac.uk/efo/EFO_0800543 GCST90140117 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arachidonoylcarnitine (C20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 arachidonoylcarnitine (C20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800544 GCST90140118 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Eicosenoylcarnitine (C20:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 eicosenoylcarnitine (C20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800545 GCST90140119 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihomo-linoleoylcarnitine (C20:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 dihomo-linoleoylcarnitine (C20:2) measurement http://www.ebi.ac.uk/efo/EFO_0800546 GCST90140120 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Chenodeoxycholic acid sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 chenodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800596 GCST90140171 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Chenodeoxycholic acid sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 chenodeoxycholic acid sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800597 GCST90140172 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Decadienedioic acid (C10:2-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90140173 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Deoxycholic acid (12 or 24)-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 deoxycholic acid (12 or 24)-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800599 GCST90140174 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphoethanolamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90140175 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Erucate (22:1n9) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 erucate (22:1n9) measurement http://www.ebi.ac.uk/efo/EFO_0800601 GCST90140176 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxy-3-methylglutarate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90140177 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Chenodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 chenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010471 GCST90140178 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ursodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90140179 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Valerate (5:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 valerate (5:0) measurement http://www.ebi.ac.uk/efo/EFO_0800603 GCST90140180 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoyl ethanolamide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 oleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800604 GCST90140181 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Butyrate/isobutyrate (4:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 isobutyrate (4:0) measurement, butyrate (4:0) measurement http://www.ebi.ac.uk/efo/EFO_0800605, http://www.ebi.ac.uk/efo/EFO_0801073 GCST90140182 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Acetoacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90140183 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Estrone 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 estrone 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800606 GCST90140184 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihomo-linoleate (20:2n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90140185 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxystearate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90140186 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycerol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90140187 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Choline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90140188 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90140189 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-palmitoyl-sphingosine (d18:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90140190 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800608 GCST90140191 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800609 GCST90140192 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-linoleoyl-gpc (16:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90140193 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Stearoyl sphingomyelin (d18:1/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 stearoyl sphingomyelin (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800611 GCST90140194 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-oleoyl-gpc (16:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90140195 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoleate (16:1n7) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90140223 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pristanate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 pristanate measurement http://www.ebi.ac.uk/efo/EFO_0800623 GCST90140224 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myristate (14:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90140225 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 12,13-DiHOME levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90140226 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Caprate (10:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 caprate 10:0 measurement http://www.ebi.ac.uk/efo/EFO_0021101 GCST90140227 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Margarate (17:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90140228 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nonadecanoate (19:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90140229 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arachidate (20:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 arachidate (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800625 GCST90140230 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-stearoyl-sphinganine (d18:0/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-stearoyl-sphinganine (d18:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800626 GCST90140231 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Caproate (6:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 caproate 6:0 measurement http://www.ebi.ac.uk/efo/EFO_0021102 GCST90140232 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Caprylate (8:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 caprylate 8:0 measurement http://www.ebi.ac.uk/efo/EFO_0021103 GCST90140233 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pentadecanoate (15:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 pentadecanoate 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021073 GCST90140234 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Xanthosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 xanthosine measurement http://www.ebi.ac.uk/efo/EFO_0010549 GCST90140235 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N1-methylinosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90140236 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N2,n2-dimethylguanosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90140237 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N4-acetylcytidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90140238 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6-carbamoylthreonyladenosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N6-carbamoylthreonyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800629 GCST90140239 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Orotidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90140240 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5,6-dihydrouridine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5,6-dihydrouridine measurement http://www.ebi.ac.uk/efo/EFO_0800631 GCST90140241 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-(3-amino-3-carboxypropyl)uridine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-(3-amino-3-carboxypropyl)uridine measurement http://www.ebi.ac.uk/efo/EFO_0800632 GCST90140242 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-methyluridine (ribothymidine) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90140243 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 7-methylguanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90140244 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methylcytidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800633 GCST90140245 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N2-methylguanosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N2-methylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0800634 GCST90140246 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6-succinyladenosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N6-succinyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021428 GCST90140247 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-beta-alanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90140248 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2'-o-methylcytidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2'-O-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800635 GCST90140249 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2'-o-methyluridine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90140250 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Allantoin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90140251 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Xanthine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90140252 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-ureidopropionate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90140253 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-aminoisobutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90140254 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5,6-dihydrouracil levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5,6-dihydrouracil measurement http://www.ebi.ac.uk/efo/EFO_0800637 GCST90140255 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Urate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90140256 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N1-methyladenosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90140257 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5,6-dihydrothymine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90140258 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hypoxanthine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90140259 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adenosine 3',5'-cyclic monophosphate (camp) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cyclic adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010473 GCST90140260 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adenosine 5'-diphosphate (ADP) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90140261 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adenosine 5'-monophosphate (AMP) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010454 GCST90140262 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6-methyladenosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N6-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800639 GCST90140263 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Beta-alanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0800640 GCST90140264 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Inosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90140265 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Inosine 5'-monophosphate (IMP) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 inosine 5'-monophosphate (IMP) measurement http://www.ebi.ac.uk/efo/EFO_0800641 GCST90140266 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Orotate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90140267 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Uridine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90140268 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2'-deoxyuridine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90140269 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adenosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 adenosine measurement http://www.ebi.ac.uk/efo/EFO_0010453 GCST90140270 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pseudouridine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90140271 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Uracil levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 uracil measurement http://www.ebi.ac.uk/efo/EFO_0800644 GCST90140272 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-stearoyl-sphingosine (d18:1/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800613 GCST90140196 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycochenodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90140197 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurochenodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90140198 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurocholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90140199 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90140200 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 9,10-DiHOME levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90140201 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleate (18:2n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90140202 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Laurate (12:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90140203 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Azelate (C9-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 azelate (C9-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800615 GCST90140204 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Eicosapentaenoate (EPA; 20:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 eicosapentaenoate (EPA; 20:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800616 GCST90140205 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arachidonate (20:4n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90140206 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxybutyrate (bhba) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90140207 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cholesterol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90140208 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Choline phosphate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90140209 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cortisone levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90140210 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90140211 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Deoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90140212 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphinganine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90140213 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glutarate (C5-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glutarate (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800620 GCST90140214 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycocholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90140215 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cortisol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90140216 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myo-inositol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90140217 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methylmalonate (mma) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 methylmalonate (MMA) measurement http://www.ebi.ac.uk/efo/EFO_0800622 GCST90140220 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitate (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90140221 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Stearate (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90140222 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cytidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90140273 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adenine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 Adenine measurement http://www.ebi.ac.uk/efo/EFO_0021573 GCST90140274 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Thymine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 thymine measurement http://www.ebi.ac.uk/efo/EFO_0800646 GCST90140275 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihydroorotate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dihydroorotate measurement http://www.ebi.ac.uk/efo/EFO_0800647 GCST90140276 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of C19H28O4 (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glucuronide of C19H28O4 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800648 GCST90140280 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of C19H28O4 (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glucuronide of C19H28O4 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800649 GCST90140281 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of C10H18O2 (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glucuronide of C10H18O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800650 GCST90140282 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of C10H18O2 (4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glucuronide of C10H18O2 (4) measurement http://www.ebi.ac.uk/efo/EFO_0800651 GCST90140285 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of C10H18O2 (7) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glucuronide of C10H18O2 (7) measurement http://www.ebi.ac.uk/efo/EFO_0800652 GCST90140286 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of C10H18O2 (8) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glucuronide of C10H18O2 (8) measurement http://www.ebi.ac.uk/efo/EFO_0800653 GCST90140287 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycine conjugate of C10H12O2 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycine conjugate of C10H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800654 GCST90140288 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycine conjugate of C10H14O2 (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 glycine conjugate of C10H14O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800655 GCST90140289 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glutamine conjugate of C7H12O2 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glutamine conjugate of C7H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800656 GCST90140290 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glutamine conjugate of C6H10O2 (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glutamine conjugate of C6H10O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800657 GCST90140291 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glutamine conjugate of C6H10O2 (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90140292 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Metabolonic lactone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90140293 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pentose acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 pentose acid measurement http://www.ebi.ac.uk/efo/EFO_0800660 GCST90140294 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) measurement http://www.ebi.ac.uk/efo/EFO_0800661 GCST90140295 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0800662 GCST90140296 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. GlcNAc sulfate conjugate of C21H34O2 steroid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 GlcNAc sulfate conjugate of C21H34O2 steroid measurement http://www.ebi.ac.uk/efo/EFO_0800663 GCST90140297 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylphenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 gamma-glutamylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021142 GCST90140298 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pyroglutamylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 pyroglutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800664 GCST90140299 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Bradykinin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 bradykinin measurement http://www.ebi.ac.uk/efo/EFO_0800665 GCST90140300 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylvaline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90140301 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pyroglutamylvaline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 pyroglutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800666 GCST90140302 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-17 36324656 Baselmans B 2021-10-06 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324656 The Genetic and Neural Substrates of Externalizing Behavior. Disruptive behavior (multivariate analysis) 523,150 European ancestry individuals NA Affymetrix [NR] 50 aggressive behaviour measurement, ADHD symptom measurement http://www.ebi.ac.uk/efo/EFO_0007826, http://www.ebi.ac.uk/efo/EFO_0007860 GCST90239692 Genome-wide genotyping array 2022-11-17 36324656 Baselmans B 2021-10-06 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324656 The Genetic and Neural Substrates of Externalizing Behavior. Risk-taking behavior (multivariate analysis) 1,506,537 European ancestry individuals NA NR [NR] 257 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST90239693 Genome-wide genotyping array 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-piperidinone levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-piperidinone measurement http://www.ebi.ac.uk/efo/EFO_0800980 GCST90140772 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indolin-2-one levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 indolin-2-one measurement http://www.ebi.ac.uk/efo/EFO_0800981 GCST90140773 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-aminophenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90140774 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-acetylphenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800983 GCST90140775 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxycotinine glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxycotinine glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800984 GCST90140776 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. S-allylcysteine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 S-allylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800985 GCST90140777 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Benzoylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 benzoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800986 GCST90140779 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylalliin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-acetylalliin measurement http://www.ebi.ac.uk/efo/EFO_0800987 GCST90140781 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-methylpipecolate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N-methylpipecolate measurement http://www.ebi.ac.uk/efo/EFO_0800988 GCST90140782 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. O-sulfo-l-tyrosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11423--O-sulfo-L-tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021231 GCST90140783 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ferulic acid 4-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ferulic acid 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800989 GCST90140784 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-(3-hydroxyphenyl)propionate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-(3-hydroxyphenyl)propionate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800990 GCST90140785 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methyl glucopyranoside (alpha + beta) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90140786 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxychlorothalonil levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-hydroxychlorothalonil measurement http://www.ebi.ac.uk/efo/EFO_0800992 GCST90140790 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isoeugenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 isoeugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800993 GCST90140791 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxycinnamate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxycinnamate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800994 GCST90140792 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxypyridine sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90140793 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-methylguaiacol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-methylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800996 GCST90140794 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methyl-4-hydroxybenzoate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90140796 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-vinylguaiacol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-vinylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800998 GCST90140797 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Eugenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 eugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800999 GCST90140798 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methoxyresorcinol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-methoxyresorcinol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801000 GCST90140799 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-acetamidophenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-acetamidophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801001 GCST90140801 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Acesulfame levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 acesulfame measurement http://www.ebi.ac.uk/efo/EFO_0801002 GCST90140802 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Syringol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 syringol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801003 GCST90140806 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Stachydrine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90140677 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. P-cresol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90140679 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Salicyluric glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 salicyluric glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0021162 GCST90140681 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 7-methylxanthine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90140683 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,3,7-trimethylurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90140684 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3,7-dimethylurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800949 GCST90140685 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,7-dimethylurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90140686 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-methylurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90140687 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-acetylamino-6-formylamino-3-methyluracil levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90140688 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-acetylamino-6-amino-3-methyluracil levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90140689 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-methylxanthine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90140690 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxyhippurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90140691 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Homostachydrine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90140692 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hydroquinone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90140693 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Catechol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90140694 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-(3-hydroxyphenyl)propionate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-(3-hydroxyphenyl)propionate measurement http://www.ebi.ac.uk/efo/EFO_0800952 GCST90140695 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ectoine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ectoine measurement http://www.ebi.ac.uk/efo/EFO_0800953 GCST90140696 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-vinylphenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90140698 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-ethylphenylsulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90140699 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Thymol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90140700 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pyrraline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90140701 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyacetaminophen sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxyacetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021153 GCST90140704 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. O-cresol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 O-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800955 GCST90140708 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-ethylphenylsulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0800956 GCST90140709 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-ethylphenylsulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0800957 GCST90140710 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21383 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21383 measurement http://www.ebi.ac.uk/efo/EFO_0800812 GCST90140522 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21410 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-21410 measurement http://www.ebi.ac.uk/efo/EFO_0800813 GCST90140523 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21441 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 7 X-21441 measurement http://www.ebi.ac.uk/efo/EFO_0800814 GCST90140524 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21442 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21442 measurement http://www.ebi.ac.uk/efo/EFO_0800815 GCST90140525 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21448 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21448 measurement http://www.ebi.ac.uk/efo/EFO_0800816 GCST90140526 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21467 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90140527 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21470 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 X-21470 measurement http://www.ebi.ac.uk/efo/EFO_0800817 GCST90140528 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21471 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 X-21471 measurement http://www.ebi.ac.uk/efo/EFO_0800818 GCST90140529 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21607 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 X-21607 measurement http://www.ebi.ac.uk/efo/EFO_0800819 GCST90140530 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21733 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21733 measurement http://www.ebi.ac.uk/efo/EFO_0800820 GCST90140532 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21736 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21736 measurement http://www.ebi.ac.uk/efo/EFO_0800821 GCST90140533 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21740 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21740 measurement http://www.ebi.ac.uk/efo/EFO_0800822 GCST90140534 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21742 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21742 measurement http://www.ebi.ac.uk/efo/EFO_0800823 GCST90140535 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21752 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21752 measurement http://www.ebi.ac.uk/efo/EFO_0800824 GCST90140536 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21796 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-21796 measurement http://www.ebi.ac.uk/efo/EFO_0800825 GCST90140537 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21803 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21803 measurement http://www.ebi.ac.uk/efo/EFO_0800826 GCST90140538 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21807 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21807 measurement http://www.ebi.ac.uk/efo/EFO_0800827 GCST90140539 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21815 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21815 measurement http://www.ebi.ac.uk/efo/EFO_0800828 GCST90140540 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21821 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21821 measurement http://www.ebi.ac.uk/efo/EFO_0800829 GCST90140541 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21829 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21829 measurement http://www.ebi.ac.uk/efo/EFO_0800830 GCST90140542 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21830 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21830 measurement http://www.ebi.ac.uk/efo/EFO_0800831 GCST90140543 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21831 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21831 measurement http://www.ebi.ac.uk/efo/EFO_0800832 GCST90140544 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21834 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21834 measurement http://www.ebi.ac.uk/efo/EFO_0800833 GCST90140545 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21839 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21839 measurement http://www.ebi.ac.uk/efo/EFO_0800834 GCST90140546 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21842 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21842 measurement http://www.ebi.ac.uk/efo/EFO_0800835 GCST90140547 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21845 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21845 measurement http://www.ebi.ac.uk/efo/EFO_0800836 GCST90140548 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21959 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21959 measurement http://www.ebi.ac.uk/efo/EFO_0800837 GCST90140549 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22143 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-22143 measurement http://www.ebi.ac.uk/efo/EFO_0800838 GCST90140550 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22162 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90140551 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22508 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-22508 measurement http://www.ebi.ac.uk/efo/EFO_0800840 GCST90140552 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25828 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25828 measurement http://www.ebi.ac.uk/efo/EFO_0800936 GCST90140650 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25937 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-25937 measurement http://www.ebi.ac.uk/efo/EFO_0800937 GCST90140651 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25957 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25957 measurement http://www.ebi.ac.uk/efo/EFO_0800938 GCST90140652 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-26054 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-26054 measurement http://www.ebi.ac.uk/efo/EFO_0800939 GCST90140653 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Benzoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90140654 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-phenylpropionate (hydrocinnamate) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90140655 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hippurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90140656 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-acetamidophenylglucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-acetamidophenylglucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800940 GCST90140657 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tartarate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90140658 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Theophylline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90140659 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Quinate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90140660 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Theobromine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90140661 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Paraxanthine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90140662 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-acetylphenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800942 GCST90140664 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Levulinate (4-oxovalerate) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 levulinate 4-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021024 GCST90140665 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Theanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 theanine measurement http://www.ebi.ac.uk/efo/EFO_0800943 GCST90140667 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tartronate (hydroxymalonate) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 tartronate (hydroxymalonate) measurement http://www.ebi.ac.uk/efo/EFO_0800944 GCST90140668 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Erythritol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90140669 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Saccharin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 saccharin measurement http://www.ebi.ac.uk/efo/EFO_0021168 GCST90140670 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Iminodiacetate (IDA) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 iminodiacetate (IDA) measurement http://www.ebi.ac.uk/efo/EFO_0800945 GCST90140671 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. EDTA levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 EDTA measurement http://www.ebi.ac.uk/efo/EFO_0800946 GCST90140672 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-(2-furoyl)glycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-(2-furoyl)glycine measurement http://www.ebi.ac.uk/efo/EFO_0800947 GCST90140673 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,3-dimethylurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90140674 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methylxanthine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90140675 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Piperine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90140676 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24462 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24462 measurement http://www.ebi.ac.uk/efo/EFO_0800886 GCST90140598 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24473 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24473 measurement http://www.ebi.ac.uk/efo/EFO_0800887 GCST90140599 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24475 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24475 measurement http://www.ebi.ac.uk/efo/EFO_0800888 GCST90140600 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24494 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-24494 measurement http://www.ebi.ac.uk/efo/EFO_0800889 GCST90140601 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24518 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-24518 measurement http://www.ebi.ac.uk/efo/EFO_0800890 GCST90140602 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24541 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24541 measurement http://www.ebi.ac.uk/efo/EFO_0800891 GCST90140603 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24544 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-24544 measurement http://www.ebi.ac.uk/efo/EFO_0800892 GCST90140604 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24546 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-24546 measurement http://www.ebi.ac.uk/efo/EFO_0800893 GCST90140605 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24549 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24549 measurement http://www.ebi.ac.uk/efo/EFO_0800894 GCST90140606 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24556 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24556 measurement http://www.ebi.ac.uk/efo/EFO_0800895 GCST90140607 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24571 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24571 measurement http://www.ebi.ac.uk/efo/EFO_0800896 GCST90140608 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24574 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-24574 measurement http://www.ebi.ac.uk/efo/EFO_0800897 GCST90140609 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24588 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-24588 measurement http://www.ebi.ac.uk/efo/EFO_0800898 GCST90140611 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24637 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24637 measurement http://www.ebi.ac.uk/efo/EFO_0800899 GCST90140612 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24657 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24657 measurement http://www.ebi.ac.uk/efo/EFO_0800900 GCST90140613 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24669 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24669 measurement http://www.ebi.ac.uk/efo/EFO_0800901 GCST90140614 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24699 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24699 measurement http://www.ebi.ac.uk/efo/EFO_0800902 GCST90140615 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24728 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24728 measurement http://www.ebi.ac.uk/efo/EFO_0800903 GCST90140616 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24736 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24736 measurement http://www.ebi.ac.uk/efo/EFO_0800904 GCST90140617 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24757 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24757 measurement http://www.ebi.ac.uk/efo/EFO_0800905 GCST90140618 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24762 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24762 measurement http://www.ebi.ac.uk/efo/EFO_0800906 GCST90140619 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24811 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-24811 measurement http://www.ebi.ac.uk/efo/EFO_0800907 GCST90140620 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24812 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24812 measurement http://www.ebi.ac.uk/efo/EFO_0800908 GCST90140621 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24849 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24849 measurement http://www.ebi.ac.uk/efo/EFO_0800909 GCST90140622 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24947 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 X-24947 measurement http://www.ebi.ac.uk/efo/EFO_0800910 GCST90140623 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23678 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23678 measurement http://www.ebi.ac.uk/efo/EFO_0800861 GCST90140573 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23680 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90140574 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23739 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90140575 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23780 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23780 measurement http://www.ebi.ac.uk/efo/EFO_0800864 GCST90140576 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23782 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23782 measurement http://www.ebi.ac.uk/efo/EFO_0800865 GCST90140577 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23787 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23787 measurement http://www.ebi.ac.uk/efo/EFO_0800866 GCST90140578 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23974 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-23974 measurement http://www.ebi.ac.uk/efo/EFO_0800867 GCST90140579 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23997 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90140580 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24295 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24295 measurement http://www.ebi.ac.uk/efo/EFO_0800869 GCST90140581 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24306 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24306 measurement http://www.ebi.ac.uk/efo/EFO_0800870 GCST90140582 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24307 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24307 measurement http://www.ebi.ac.uk/efo/EFO_0800871 GCST90140583 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24309 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-24309 measurement http://www.ebi.ac.uk/efo/EFO_0800872 GCST90140584 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24328 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-24328 measurement http://www.ebi.ac.uk/efo/EFO_0800873 GCST90140585 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24334 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24334 measurement http://www.ebi.ac.uk/efo/EFO_0800874 GCST90140586 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24337 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-24337 measurement http://www.ebi.ac.uk/efo/EFO_0800875 GCST90140587 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24344 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24344 measurement http://www.ebi.ac.uk/efo/EFO_0800876 GCST90140588 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24352 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24352 measurement http://www.ebi.ac.uk/efo/EFO_0800877 GCST90140589 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24411 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24411 measurement http://www.ebi.ac.uk/efo/EFO_0800878 GCST90140590 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24418 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-24418 measurement http://www.ebi.ac.uk/efo/EFO_0800879 GCST90140591 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24422 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-24422 measurement http://www.ebi.ac.uk/efo/EFO_0800880 GCST90140592 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24425 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24425 measurement http://www.ebi.ac.uk/efo/EFO_0800881 GCST90140593 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24431 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24431 measurement http://www.ebi.ac.uk/efo/EFO_0800882 GCST90140594 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24432 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24432 measurement http://www.ebi.ac.uk/efo/EFO_0800883 GCST90140595 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24455 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24455 measurement http://www.ebi.ac.uk/efo/EFO_0800884 GCST90140596 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24456 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24456 measurement http://www.ebi.ac.uk/efo/EFO_0800885 GCST90140597 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24949 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-24949 measurement http://www.ebi.ac.uk/efo/EFO_0800911 GCST90140624 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24951 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24951 measurement http://www.ebi.ac.uk/efo/EFO_0800912 GCST90140625 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24970 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24970 measurement http://www.ebi.ac.uk/efo/EFO_0800913 GCST90140626 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24972 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24972 measurement http://www.ebi.ac.uk/efo/EFO_0800914 GCST90140627 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-24980 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-24980 measurement http://www.ebi.ac.uk/efo/EFO_0800915 GCST90140628 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25172 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25172 measurement http://www.ebi.ac.uk/efo/EFO_0800916 GCST90140629 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25265 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25265 measurement http://www.ebi.ac.uk/efo/EFO_0800917 GCST90140630 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25266 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25266 measurement http://www.ebi.ac.uk/efo/EFO_0800918 GCST90140631 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25267 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25267 measurement http://www.ebi.ac.uk/efo/EFO_0800919 GCST90140632 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25271 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25271 measurement http://www.ebi.ac.uk/efo/EFO_0800920 GCST90140633 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25279 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25279 measurement http://www.ebi.ac.uk/efo/EFO_0800921 GCST90140634 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25343 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25343 measurement http://www.ebi.ac.uk/efo/EFO_0800922 GCST90140635 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25371 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-25371 measurement http://www.ebi.ac.uk/efo/EFO_0800923 GCST90140636 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25417 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25417 measurement http://www.ebi.ac.uk/efo/EFO_0800924 GCST90140637 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25419 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-25419 measurement http://www.ebi.ac.uk/efo/EFO_0800925 GCST90140638 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25420 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25420 measurement http://www.ebi.ac.uk/efo/EFO_0800926 GCST90140639 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25422 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-25422 measurement http://www.ebi.ac.uk/efo/EFO_0800927 GCST90140640 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25433 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-25433 measurement http://www.ebi.ac.uk/efo/EFO_0800928 GCST90140641 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25503 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25503 measurement http://www.ebi.ac.uk/efo/EFO_0800929 GCST90140642 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25519 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25519 measurement http://www.ebi.ac.uk/efo/EFO_0800930 GCST90140643 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25520 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25520 measurement http://www.ebi.ac.uk/efo/EFO_0800931 GCST90140644 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25617 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25617 measurement http://www.ebi.ac.uk/efo/EFO_0800932 GCST90140645 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25790 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-25790 measurement http://www.ebi.ac.uk/efo/EFO_0800933 GCST90140646 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25793 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25793 measurement http://www.ebi.ac.uk/efo/EFO_0800934 GCST90140647 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-25802 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-25802 measurement http://www.ebi.ac.uk/efo/EFO_0800935 GCST90140648 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22509 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-22509 measurement http://www.ebi.ac.uk/efo/EFO_0800841 GCST90140553 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22519 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-22519 measurement http://www.ebi.ac.uk/efo/EFO_0800842 GCST90140554 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22520 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-22520 measurement http://www.ebi.ac.uk/efo/EFO_0800843 GCST90140555 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22771 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-22771 measurement http://www.ebi.ac.uk/efo/EFO_0800844 GCST90140556 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-22776 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-22776 measurement http://www.ebi.ac.uk/efo/EFO_0800845 GCST90140557 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23157 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23157 measurement http://www.ebi.ac.uk/efo/EFO_0800846 GCST90140558 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23276 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23276 measurement http://www.ebi.ac.uk/efo/EFO_0800847 GCST90140559 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23583 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23583 measurement http://www.ebi.ac.uk/efo/EFO_0800848 GCST90140560 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23587 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23587 measurement http://www.ebi.ac.uk/efo/EFO_0800849 GCST90140561 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23590 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23590 measurement http://www.ebi.ac.uk/efo/EFO_0800850 GCST90140562 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23593 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23593 measurement http://www.ebi.ac.uk/efo/EFO_0800851 GCST90140563 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23636 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23636 measurement http://www.ebi.ac.uk/efo/EFO_0800852 GCST90140564 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23639 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90140565 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23641 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-23641 measurement http://www.ebi.ac.uk/efo/EFO_0800854 GCST90140566 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23644 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23644 measurement http://www.ebi.ac.uk/efo/EFO_0800855 GCST90140567 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23655 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23655 measurement http://www.ebi.ac.uk/efo/EFO_0800856 GCST90140568 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23657 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23657 measurement http://www.ebi.ac.uk/efo/EFO_0800857 GCST90140569 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23662 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23662 measurement http://www.ebi.ac.uk/efo/EFO_0800858 GCST90140570 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23665 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-23665 measurement http://www.ebi.ac.uk/efo/EFO_0800859 GCST90140571 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-23666 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-23666 measurement http://www.ebi.ac.uk/efo/EFO_0800860 GCST90140572 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adrenate (22:4n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90139728 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 10-undecenoate (11:1n1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90139729 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myristoleate (14:1n5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90139730 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sebacate (C10-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90139731 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Stearidonate (18:4n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90139732 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-dodecenoate (12:1n7) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5-dodecenoate 12:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021100 GCST90139733 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Octanoylcarnitine (c8) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90139734 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tauro-beta-muricholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tauro-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800213 GCST90139735 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Decanoylcarnitine (C10) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90139736 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-GPC (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800214 GCST90139737 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-margaroyl-GPC (17:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-margaroyl-GPC (17:0) measurement http://www.ebi.ac.uk/efo/EFO_0800215 GCST90139738 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Campesterol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90139739 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myristoylcarnitine (C14) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90139740 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-gpc (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-stearoyl-GPC (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800217 GCST90139741 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-GPC (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800218 GCST90139742 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 10-nonadecenoate (19:1n9) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90139743 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 10-heptadecenoate (17:1n7) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 10-heptadecenoate 17:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021060 GCST90139744 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hyocholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 hyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800219 GCST90139745 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Epiandrosterone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90139746 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Eicosenoate (20:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 eicosenoate (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800220 GCST90139747 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-oleoylglycerol (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800196 GCST90139707 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-myristoyl-GPC (14:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-myristoyl-GPC (14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800221 GCST90139749 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoylglycerol (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800199 GCST90139710 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-palmitoylglycerol (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-palmitoylglycerol (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800200 GCST90139711 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Stearoylcarnitine (C18) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90139751 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycolithocholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycolithocholate measurement http://www.ebi.ac.uk/efo/EFO_0800203 GCST90139714 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androsterone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90139716 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dodecanedioate (C12-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90139717 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxylaurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3-hydroxylaurate measurement http://www.ebi.ac.uk/efo/EFO_0800204 GCST90139718 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxysebacate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800205 GCST90139719 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-hydroxyhexanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800206 GCST90139720 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Propionylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 propionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800207 GCST90139721 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Butyrylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 butyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800208 GCST90139722 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-linoleoyl-GPE (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 2-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800264 GCST90139803 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-GPI (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-oleoyl-GPI (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800265 GCST90139804 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-GPI (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-linoleoyl-GPI (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800266 GCST90139805 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoleoyl-GPE (16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoleoyl-GPE (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800267 GCST90139806 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoleoyl-GPI (16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoleoyl-GPI (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800268 GCST90139807 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-oleoyl-GPE (18:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 1-stearoyl-2-oleoyl-GPE (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800269 GCST90139808 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Chiro-inositol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 chiro-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800270 GCST90139809 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90139810 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800272 GCST90139811 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-arachidonoyl-GPS (18:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-stearoyl-2-arachidonoyl-GPS (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800273 GCST90139812 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphinganine-1-phosphate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sphinganine-1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800274 GCST90139813 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 glycosyl-N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800275 GCST90139814 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3beta,17beta-diol disulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90139815 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-pregnan-3beta,20alpha-diol disulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-11445--5-alpha-pregnan-3beta,20alpha-disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021238 GCST90139816 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycocholenate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90139817 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurocholenate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90139818 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androstenediol (3beta,17beta) disulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 androstenediol (3beta,17beta) disulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800278 GCST90139819 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pregnenediol disulfate (C21H34O8S2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 pregnenediol disulfate (C21H34O8S2) measurement http://www.ebi.ac.uk/efo/EFO_0800279 GCST90139820 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androstenediol (3beta,17beta) disulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 androstenediol (3beta,17beta) disulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800280 GCST90139821 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 21-hydroxypregnenolone disulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90139822 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 21-hydroxypregnenolone monosulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 21-hydroxypregnenolone monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800282 GCST90139823 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3alpha,17alpha-diol monosulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 5alpha-androstan-3alpha,17alpha-diol monosulfate measurement http://www.ebi.ac.uk/efo/EFO_0800283 GCST90139824 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800284 GCST90139825 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800285 GCST90139826 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-pregnan-diol disulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90139827 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-GPE (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800246 GCST90139778 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-GPE (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800247 GCST90139779 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-arachidonoyl-GPE (20:4n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-arachidonoyl-GPE (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800248 GCST90139780 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxypalmitate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90139781 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosapentaenoate (n6 DPA; 22:5n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 docosapentaenoate (n6 DPA; 22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800249 GCST90139782 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methylmalonylcarnitine (C4-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-methylmalonylcarnitine (C4-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800250 GCST90139783 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 7-alpha-hydroxy-3-oxo-4-cholestenoate 7-Hoca measurement http://www.ebi.ac.uk/efo/EFO_0021116 GCST90139784 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3beta,7alpha-dihydroxy-5-cholestenoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3beta,7alpha-dihydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800251 GCST90139785 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tetradecanedioate (C14-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90139786 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hexadecanedioate (C16-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90139787 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Octadecanedioate (C18-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90139788 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-myristoylglycerol (14:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-myristoylglycerol (14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800252 GCST90139789 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycerophosphoethanolamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90139790 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-oleoyl-GPE (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800254 GCST90139791 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-palmitoyl-GPE (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800255 GCST90139792 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-arachidonoyl-GPI (20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-arachidonoyl-GPI (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800256 GCST90139793 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-GPI (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-GPI (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800257 GCST90139794 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycolithocholate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90139795 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurolithocholate 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90139796 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Deoxycarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90139797 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-arachidonoyl-GPE (20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 2-arachidonoyl-GPE (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800260 GCST90139798 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-hydroxycaproate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 alpha-hydroxycaproate measurement http://www.ebi.ac.uk/efo/EFO_0800261 GCST90139799 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hexanoylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 hexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800262 GCST90139800 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihomo-linolenate (20:3n3 or n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90139801 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methyladipate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90139802 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-CEHC glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800165 GCST90139652 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-CEHC sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 alpha-CEHC sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800166 GCST90139653 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-CMBHC glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 alpha-CMBHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800167 GCST90139654 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-tocopherol/beta-tocopherol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-tocopherol measurement, beta-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007899, http://www.ebi.ac.uk/efo/EFO_0800168 GCST90139655 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ascorbic acid 2-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 ascorbic acid 2-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800169 GCST90139656 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Carotene diol (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 carotene diol (1) measurement http://www.ebi.ac.uk/efo/EFO_0800170 GCST90139657 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Carotene diol (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 carotene diol (2) measurement http://www.ebi.ac.uk/efo/EFO_0800171 GCST90139658 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Carotene diol (3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 carotene diol (3) measurement http://www.ebi.ac.uk/efo/EFO_0800172 GCST90139659 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ascorbic acid 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 7 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90139660 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Delta-CEHC levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 delta-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800174 GCST90139661 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pantothenate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90139662 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Bilirubin (z,z) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90139663 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-tocopherol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90139664 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Quinolinate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90139665 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adenosine 5'-diphosphoribose (ADP-ribose) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 adenosine 5'-diphosphoribose (ADP-ribose) measurement http://www.ebi.ac.uk/efo/EFO_0800176 GCST90139666 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Biliverdin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90139667 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Flavin adenine dinucleotide (FAD) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 flavin adenine dinucleotide (FAD) measurement http://www.ebi.ac.uk/efo/EFO_0800177 GCST90139668 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nicotinamide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90139669 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Retinol (Vitamin A) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90139670 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-methylnicotinamide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90139671 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Aconitate [cis or trans] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90139672 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Succinylcarnitine (c4-dc) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90139673 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methylcitrate/homocitrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-methylcitrate measurement, homocitrate measurement http://www.ebi.ac.uk/efo/EFO_0801071, http://www.ebi.ac.uk/efo/EFO_0800179 GCST90139674 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isocitric lactone levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 isocitric lactone measurement http://www.ebi.ac.uk/efo/EFO_0800180 GCST90139675 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Citrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90139676 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Succinate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90139677 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Fumarate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90139678 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Malate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90139679 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90139680 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-ketoglutarate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90139681 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Carnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90139682 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Suberate (C8-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90139683 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycerol 3-phosphate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90139684 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycerophosphorylcholine (GPC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90139685 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90139686 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-arachidonoylglycerol (20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-arachidonoylglycerol (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800182 GCST90139687 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmityl-GPC (o-16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmityl-GPC (O-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800183 GCST90139688 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800184 GCST90139689 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingosine 1-phosphate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90139690 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-GPS (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-oleoyl-GPS (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800186 GCST90139691 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-oleoyl-GPS (18:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-stearoyl-2-oleoyl-GPS (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800187 GCST90139692 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-GPI (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800188 GCST90139693 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,2-dipalmitoyl-gpc (16:0/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1,2-dipalmitoyl-GPC (16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800189 GCST90139694 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,2-distearoyl-GPC (18:0/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1,2-distearoyl-GPC (18:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800190 GCST90139695 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosahexaenoate (DHA; 22:6n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90139696 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-myristoyl-2-palmitoyl-gpc (14:0/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800191 GCST90139697 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Maleate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90139698 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyoctanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90139699 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyoctanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800193 GCST90139700 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoylcarnitine (C16) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90139701 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-gpc (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800223 GCST90139753 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-arachidonylglycerol (20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-arachidonylglycerol (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800224 GCST90139754 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linolenoylglycerol (18:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-linolenoylglycerol (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800225 GCST90139755 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxydodecanedioate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxydodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0800226 GCST90139756 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-GPE (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 1-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800227 GCST90139757 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-GPG (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-stearoyl-GPG (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800228 GCST90139758 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-docosahexaenoylglycerol (22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-docosahexaenoylglycerol (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800229 GCST90139759 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-dihomo-linoleoylglycerol (20:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-dihomo-linoleoylglycerol (20:2) measurement http://www.ebi.ac.uk/efo/EFO_0800230 GCST90139760 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoylcarnitine (C18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90139761 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoleoyl-GPC (16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800231 GCST90139762 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Malonylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 malonylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800232 GCST90139763 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hexanoylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 hexanoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800233 GCST90139764 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Testosterone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90139765 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-arachidonoyl-gpc (20:4n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-arachidonoyl-GPC (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800234 GCST90139766 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-dihomo-linolenoyl-GPC (20:3n3 or 6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-dihomo-linolenoyl-GPC (20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800235 GCST90139767 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-dihomo-linoleoyl-GPC (20:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-dihomo-linoleoyl-GPC (20:2) measurement http://www.ebi.ac.uk/efo/EFO_0800236 GCST90139768 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-arachidonoyl-GPC (20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-arachidonoyl-GPC (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800237 GCST90139769 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-oleoyl-GPC (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800238 GCST90139770 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-linoleoyl-GPC (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800239 GCST90139771 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-palmitoleoyl-GPC (16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800240 GCST90139772 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-palmitoyl-GPC (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800241 GCST90139773 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-myristoyl-GPC (14:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 2-myristoyl-GPC (14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800242 GCST90139774 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-docosahexaenoyl-GPC (22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-docosahexaenoyl-GPC (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800243 GCST90139775 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-docosahexaenoyl-GPC (22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-docosahexaenoyl-GPC (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800244 GCST90139776 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-GPE (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800245 GCST90139777 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hexanoylcarnitine (C6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90139702 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dehydroepiandrosterone sulfate (DHEA-S) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90139703 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Acetylcarnitine (c2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90139704 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoylglycerol (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoylglycerol (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800194 GCST90139705 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoylglycerol (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800195 GCST90139706 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linolenate [alpha or gamma; (18:3n3 or 6)] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90139748 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-linoleoylglycerol (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800197 GCST90139708 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxydecanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800198 GCST90139709 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-arachidoyl-GPC (20:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-arachidoyl-GPC (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800222 GCST90139750 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Butyrylcarnitine (C4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 butyrylcarnitine (C4) measurement http://www.ebi.ac.uk/efo/EFO_0800201 GCST90139712 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 7-ketodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 7-ketodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800202 GCST90139713 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Laurylcarnitine (C12) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90139752 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyadipate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxyadipate measurement http://www.ebi.ac.uk/efo/EFO_0800209 GCST90139723 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Propionylcarnitine (c3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 propionylcarnitine (C3) measurement http://www.ebi.ac.uk/efo/EFO_0800210 GCST90139724 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90139725 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosapentaenoate (n3 DPA; 22:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 docosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0006809 GCST90139726 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosadienoate (22:2n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 docosadienoate (22:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800211 GCST90139727 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-03 36267138 Alotaibi RN 2022-01-04 Front Dent Med www.ncbi.nlm.nih.gov/pubmed/36267138 Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort. Dental anomalies (Tooth Agenesis, impaction and Rotation) 3,579 individuals NA Illumina [5802671] (imputed) 5 Abnormality of the dentition http://purl.obolibrary.org/obo/HP_0000164 GCST90204169 Genome-wide genotyping array 2022-11-03 36267138 Alotaibi RN 2022-01-04 Front Dent Med www.ncbi.nlm.nih.gov/pubmed/36267138 Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort. Dental anomalies (Hypoplasia, displacement and rotation) 3,579 individuals NA Illumina [5802671] (imputed) 4 Abnormality of the dentition http://purl.obolibrary.org/obo/HP_0000164 GCST90204170 Genome-wide genotyping array 2022-11-03 36267138 Alotaibi RN 2022-01-04 Front Dent Med www.ncbi.nlm.nih.gov/pubmed/36267138 Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort. Dental anomalies (Displacement, Rotation and Mamelon) 3,579 individuals NA Illumina [5802671] (imputed) 4 Abnormality of the dentition http://purl.obolibrary.org/obo/HP_0000164 GCST90204171 Genome-wide genotyping array 2022-11-03 36267138 Alotaibi RN 2022-01-04 Front Dent Med www.ncbi.nlm.nih.gov/pubmed/36267138 Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort. Dental caries, Agenesis and Hypoplasia 3,579 individuals NA Illumina [5802671] (imputed) 5 Dental enamel hypoplasia, dental caries, tooth agenesis http://www.ebi.ac.uk/efo/EFO_1001304, http://www.ebi.ac.uk/efo/EFO_0003819, http://www.ebi.ac.uk/efo/EFO_0005410 GCST90204172 Genome-wide genotyping array 2022-12-13 36327221 Wang Y 2022-11-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36327221 COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection. Severe COVID-19 or systemic lupus erythematosus (inverse variance) 6,956 European ancestry severe COVID-19 cases, 1,823 severe COVID-19 cases, 9,302 European ancestry SLE cases, 1,024,729 European ancestry controls, 328,311 controls NA NR [1559546] (imputed) 6 systemic lupus erythematosus, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007915, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90243963 Genome-wide genotyping array 2022-12-13 36327221 Wang Y 2022-11-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36327221 COVID-19 and systemic lupus erythematosus genetics: A balance between autoimmune disease risk and protection against infection. Severe COVID-19 or systemic lupus erythematosus 6,956 European ancestry severe COVID-19 cases, 1,823 severe COVID-19 cases, 9,302 European ancestry SLE cases, 1,024,729 European ancestry controls, 328,311 controls NA NR [1559546] (imputed) 9 systemic lupus erythematosus, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007915, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90243962 Genome-wide genotyping array 2022-10-25 36164742 Jung S 2022-09-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36164742 Case-case genome-wide association analysis identifying genetic loci with divergent effects on Crohn's disease and ulcerative colitis. Crohn's disease vs ulcerative colitis 2,359 Korean ancestry crohn's disease cases, 2,175 Korean ancestry ulcerative colitis cases 772 Korean ancestry crohn's disease cases, 619 Korean ancestry ulcerative colitis cases Illumina [2765594] (imputed) 3 ulcerative colitis, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90179177 Genome-wide genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Neutrophil granulocyte count 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 2 granulocyte count http://www.ebi.ac.uk/efo/EFO_0007987 GCST90188372 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Neutrophil granulocyte count percentage 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 0 neutrophil percentage of granulocytes http://www.ebi.ac.uk/efo/EFO_0007994 GCST90188373 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Hematocrit 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90188374 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Hemoglobin concentration 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90188375 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Lymphocyte count 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90188376 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Lymphocyte count percentage 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 0 lymphocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007993 GCST90188377 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Mean corpuscular hemoglobin 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 2 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90188378 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Mean corpuscular hemoglobin concentration 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90188379 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Mean corpuscular volume 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 3 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90188380 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Mean platelet volume 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 6 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90188383 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Platelet count 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 4 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90002413 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Red blood cell count 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 1 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90188385 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. Red blood cell distribution width coefficient of variation 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 2 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90188386 Exome genotyping array 2022-11-15 33693786 Sun P 2021-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33693786 An Asian-specific MPL genetic variant alters JAK-STAT signaling and influences platelet count in the population. White blood cell count 5,257 Han Chinese ancestry individuals 3,827 Chinese ancestry individuals Illumina [84841] 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90188387 Exome genotyping array 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Prolylproline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 prolylproline measurement http://www.ebi.ac.uk/efo/EFO_0800684 GCST90140334 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Prolylserine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 prolylserine measurement http://www.ebi.ac.uk/efo/EFO_0800685 GCST90140335 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylacetylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phenylacetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800686 GCST90140336 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylacetylglutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 phenylacetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800687 GCST90140337 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxyphenylacetylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90140338 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamyl-alpha-lysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90140339 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylcitrulline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-glutamylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800690 GCST90140341 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamyltyrosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90140345 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90140346 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylhistidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90140347 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90140348 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylglutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90140349 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-07765 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90140350 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-10458 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-10458 measurement http://www.ebi.ac.uk/efo/EFO_0800692 GCST90140351 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11261 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-11261 measurement http://www.ebi.ac.uk/efo/EFO_0021221 GCST90140352 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11299 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90140353 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11308 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-11308 measurement http://www.ebi.ac.uk/efo/EFO_0800693 GCST90140354 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11315 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90140355 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11372 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11372 measurement http://www.ebi.ac.uk/efo/EFO_0800694 GCST90140356 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11378 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11378 measurement http://www.ebi.ac.uk/efo/EFO_0800695 GCST90140357 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11381 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90140358 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11441 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11441 measurement http://www.ebi.ac.uk/efo/EFO_0021235 GCST90140359 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11442 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11442 measurement http://www.ebi.ac.uk/efo/EFO_0021236 GCST90140360 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11444 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90140361 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11470 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90140362 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamyl-epsilon-lysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-glutamyl-epsilon-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800667 GCST90140303 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycylphenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800668 GCST90140304 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. HWESASLLR levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 HWESASLLR measurement http://www.ebi.ac.uk/efo/EFO_0800669 GCST90140305 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Bradykinin, des-arg(9) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 bradykinin, des-arg 9 measurement http://www.ebi.ac.uk/efo/EFO_0021146 GCST90140306 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90140307 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamyltryptophan levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 gamma-glutamyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800671 GCST90140308 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylmethionine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90140309 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylthreonine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90140310 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Fibrinopeptide A levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 fibrinopeptide A measurement http://www.ebi.ac.uk/efo/EFO_0800672 GCST90140311 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Fibrinopeptide A, des-ala(1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 fibrinopeptide A, des-ala(1) measurement http://www.ebi.ac.uk/efo/EFO_0800673 GCST90140312 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. HWESASXX levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 HWESASXX measurement http://www.ebi.ac.uk/efo/EFO_0021147 GCST90140314 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylacetylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90140316 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylisoleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90140317 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamyl-2-aminobutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90140318 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Leucylleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 leucylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021130 GCST90140319 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-glutamylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-glutamylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800675 GCST90140320 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cyclo(leu-pro) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 cyclo(leu-pro) measurement http://www.ebi.ac.uk/efo/EFO_0800676 GCST90140321 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylalanylphenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 phenylalanylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021131 GCST90140322 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isoleucylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 isoleucylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800677 GCST90140323 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Leucylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 leucylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800678 GCST90140325 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylalanyltryptophan levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 phenylalanyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800679 GCST90140327 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Valylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 valylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800680 GCST90140330 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Valylphenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 valylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800681 GCST90140331 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methionylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 methionylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800682 GCST90140332 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Prolylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 prolylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800683 GCST90140333 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16935 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-16935 measurement http://www.ebi.ac.uk/efo/EFO_0800763 GCST90140465 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16938 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-16938 measurement http://www.ebi.ac.uk/efo/EFO_0800764 GCST90140466 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16944 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-16944 measurement http://www.ebi.ac.uk/efo/EFO_0800765 GCST90140467 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16946 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-16946 measurement http://www.ebi.ac.uk/efo/EFO_0800766 GCST90140468 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16964 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-16964 measurement http://www.ebi.ac.uk/efo/EFO_0020011 GCST90140469 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17010 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17010 measurement http://www.ebi.ac.uk/efo/EFO_0800767 GCST90140470 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17137 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17137 measurement http://www.ebi.ac.uk/efo/EFO_0800768 GCST90140471 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17162 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17162 measurement http://www.ebi.ac.uk/efo/EFO_0800769 GCST90140472 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17185 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17185 measurement http://www.ebi.ac.uk/efo/EFO_0800770 GCST90140473 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17325 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-17325 measurement http://www.ebi.ac.uk/efo/EFO_0800771 GCST90140474 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17335 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90140475 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17340 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-17340 measurement http://www.ebi.ac.uk/efo/EFO_0800773 GCST90140476 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17351 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17351 measurement http://www.ebi.ac.uk/efo/EFO_0800774 GCST90140480 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17353 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17353 measurement http://www.ebi.ac.uk/efo/EFO_0800775 GCST90140481 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17354 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17354 measurement http://www.ebi.ac.uk/efo/EFO_0800776 GCST90140482 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17357 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-17357 measurement http://www.ebi.ac.uk/efo/EFO_0800777 GCST90140484 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17361 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17361 measurement http://www.ebi.ac.uk/efo/EFO_0800778 GCST90140485 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17367 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17367 measurement http://www.ebi.ac.uk/efo/EFO_0800779 GCST90140486 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17371 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17371 measurement http://www.ebi.ac.uk/efo/EFO_0800780 GCST90140487 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17438 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17438 measurement http://www.ebi.ac.uk/efo/EFO_0800781 GCST90140489 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17612 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-17612 measurement http://www.ebi.ac.uk/efo/EFO_0800782 GCST90140490 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17653 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-17653 measurement http://www.ebi.ac.uk/efo/EFO_0800783 GCST90140491 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17654 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 X-17654 measurement http://www.ebi.ac.uk/efo/EFO_0800784 GCST90140492 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17676 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90140493 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17685 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17685 measurement http://www.ebi.ac.uk/efo/EFO_0800786 GCST90140494 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17686 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17686 measurement http://www.ebi.ac.uk/efo/EFO_0800787 GCST90140495 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-17690 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-17690 measurement http://www.ebi.ac.uk/efo/EFO_0800788 GCST90140496 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18345 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-18345 measurement http://www.ebi.ac.uk/efo/EFO_0800789 GCST90140498 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18886 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-18886 measurement http://www.ebi.ac.uk/efo/EFO_0800790 GCST90140499 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18887 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-18887 measurement http://www.ebi.ac.uk/efo/EFO_0800791 GCST90140500 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18888 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-18888 measurement http://www.ebi.ac.uk/efo/EFO_0800792 GCST90140501 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18899 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-18899 measurement http://www.ebi.ac.uk/efo/EFO_0800793 GCST90140502 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18901 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-18901 measurement http://www.ebi.ac.uk/efo/EFO_0800794 GCST90140503 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18913 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-18913 measurement http://www.ebi.ac.uk/efo/EFO_0800795 GCST90140504 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18921 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-18921 measurement http://www.ebi.ac.uk/efo/EFO_0800796 GCST90140505 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18922 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-18922 measurement http://www.ebi.ac.uk/efo/EFO_0800797 GCST90140506 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-18935 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-18935 measurement http://www.ebi.ac.uk/efo/EFO_0800798 GCST90140507 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-19141 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-19141 measurement http://www.ebi.ac.uk/efo/EFO_0800799 GCST90140508 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-19183 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-19183 measurement http://www.ebi.ac.uk/efo/EFO_0800800 GCST90140509 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-19438 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-19438 measurement http://www.ebi.ac.uk/efo/EFO_0800801 GCST90140510 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21258 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21258 measurement http://www.ebi.ac.uk/efo/EFO_0800802 GCST90140511 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21285 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-21285 measurement http://www.ebi.ac.uk/efo/EFO_0800803 GCST90140512 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21286 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21286 measurement http://www.ebi.ac.uk/efo/EFO_0800804 GCST90140513 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21310 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21310 measurement http://www.ebi.ac.uk/efo/EFO_0800805 GCST90140514 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21312 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21312 measurement http://www.ebi.ac.uk/efo/EFO_0800806 GCST90140515 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21319 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90140517 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21339 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21339 measurement http://www.ebi.ac.uk/efo/EFO_0800808 GCST90140518 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21353 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21353 measurement http://www.ebi.ac.uk/efo/EFO_0800809 GCST90140519 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21355 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-21355 measurement http://www.ebi.ac.uk/efo/EFO_0800810 GCST90140520 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-21364 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90140521 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13726 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13726 measurement http://www.ebi.ac.uk/efo/EFO_0800740 GCST90140440 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13728 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13728 measurement http://www.ebi.ac.uk/efo/EFO_0800741 GCST90140441 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13729 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-13729 measurement http://www.ebi.ac.uk/efo/EFO_0800742 GCST90140442 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13835 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13835 measurement http://www.ebi.ac.uk/efo/EFO_0800743 GCST90140443 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13844 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-13844 measurement http://www.ebi.ac.uk/efo/EFO_0800744 GCST90140444 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13866 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90140445 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-14056 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90140446 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-14082 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-14082 measurement http://www.ebi.ac.uk/efo/EFO_0800746 GCST90140447 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-14939 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-14939 measurement http://www.ebi.ac.uk/efo/EFO_0800747 GCST90140448 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15245 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-15245 measurement http://www.ebi.ac.uk/efo/EFO_0800748 GCST90140449 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15461 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-15461 measurement http://www.ebi.ac.uk/efo/EFO_0800749 GCST90140450 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15469 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-15469 measurement http://www.ebi.ac.uk/efo/EFO_0800750 GCST90140451 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15486 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90140452 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15492 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-15492 measurement http://www.ebi.ac.uk/efo/EFO_0800752 GCST90140453 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15503 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-15503 measurement http://www.ebi.ac.uk/efo/EFO_0800753 GCST90140454 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15666 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-15666 measurement http://www.ebi.ac.uk/efo/EFO_0800754 GCST90140455 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15674 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-15674 measurement http://www.ebi.ac.uk/efo/EFO_0800755 GCST90140456 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-15728 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-15728 measurement http://www.ebi.ac.uk/efo/EFO_0020024 GCST90140457 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16087 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-16087 measurement http://www.ebi.ac.uk/efo/EFO_0800756 GCST90140458 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16124 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-16124 measurement http://www.ebi.ac.uk/efo/EFO_0800757 GCST90140459 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16397 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-16397 measurement http://www.ebi.ac.uk/efo/EFO_0800758 GCST90140460 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16570 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-16570 measurement http://www.ebi.ac.uk/efo/EFO_0800759 GCST90140461 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16576 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-16576 measurement http://www.ebi.ac.uk/efo/EFO_0800760 GCST90140462 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16580 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90140463 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-16649 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-16649 measurement http://www.ebi.ac.uk/efo/EFO_0800762 GCST90140464 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12730 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12730 measurement http://www.ebi.ac.uk/efo/EFO_0800724 GCST90140414 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12731 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12731 measurement http://www.ebi.ac.uk/efo/EFO_0800725 GCST90140415 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12738 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12738 measurement http://www.ebi.ac.uk/efo/EFO_0800726 GCST90140416 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12740 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90140417 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12753 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12753 measurement http://www.ebi.ac.uk/efo/EFO_0800727 GCST90140418 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12798 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90140419 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12812 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12812 measurement http://www.ebi.ac.uk/efo/EFO_0800728 GCST90140420 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12816 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12816 measurement http://www.ebi.ac.uk/efo/EFO_0021336 GCST90140422 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12818 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12818 measurement http://www.ebi.ac.uk/efo/EFO_0800729 GCST90140423 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12822 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12822 measurement http://www.ebi.ac.uk/efo/EFO_0800730 GCST90140424 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12830 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12830 measurement http://www.ebi.ac.uk/efo/EFO_0021337 GCST90140425 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12839 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12839 measurement http://www.ebi.ac.uk/efo/EFO_0800731 GCST90140426 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12844 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90140427 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12847 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90140428 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12849 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12849 measurement http://www.ebi.ac.uk/efo/EFO_0800732 GCST90140429 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12851 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12851 measurement http://www.ebi.ac.uk/efo/EFO_0021342 GCST90140430 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12906 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12906 measurement http://www.ebi.ac.uk/efo/EFO_0800733 GCST90140431 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13007 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13007 measurement http://www.ebi.ac.uk/efo/EFO_0800734 GCST90140432 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13431 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90140433 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13507 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13507 measurement http://www.ebi.ac.uk/efo/EFO_0800736 GCST90140434 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13553 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 X-13553 measurement http://www.ebi.ac.uk/efo/EFO_0021355 GCST90140435 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13658 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13658 measurement http://www.ebi.ac.uk/efo/EFO_0021357 GCST90140436 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13684 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90140437 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13695 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13695 measurement http://www.ebi.ac.uk/efo/EFO_0800738 GCST90140438 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-13723 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-13723 measurement http://www.ebi.ac.uk/efo/EFO_0800739 GCST90140439 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11478 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90140363 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11483 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90140364 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11522 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11522 measurement http://www.ebi.ac.uk/efo/EFO_0800696 GCST90140365 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11530 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11530 measurement http://www.ebi.ac.uk/efo/EFO_0021249 GCST90140366 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11632 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11632 measurement http://www.ebi.ac.uk/efo/EFO_0800697 GCST90140367 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11787 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90140368 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11795 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90140369 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11843 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90140370 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11847 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90140371 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11849 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90140372 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11850 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90140373 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11852 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90140374 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11858 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90140375 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-11880 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-11880 measurement http://www.ebi.ac.uk/efo/EFO_0800698 GCST90140376 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12007 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90140377 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12013 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90140378 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12015 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12015 measurement http://www.ebi.ac.uk/efo/EFO_0800699 GCST90140379 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12026 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-12026 measurement http://www.ebi.ac.uk/efo/EFO_0800700 GCST90140380 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12100 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-12100 measurement http://www.ebi.ac.uk/efo/EFO_0800701 GCST90140381 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12101 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90140382 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12104 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12104 measurement http://www.ebi.ac.uk/efo/EFO_0800703 GCST90140383 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12111 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12111 measurement http://www.ebi.ac.uk/efo/EFO_0800704 GCST90140384 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12112 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-12112 measurement http://www.ebi.ac.uk/efo/EFO_0800705 GCST90140385 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12117 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-12117 measurement http://www.ebi.ac.uk/efo/EFO_0800706 GCST90140386 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12125 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12125 measurement http://www.ebi.ac.uk/efo/EFO_0800707 GCST90140387 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12126 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12126 measurement http://www.ebi.ac.uk/efo/EFO_0800708 GCST90140388 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12127 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12127 measurement http://www.ebi.ac.uk/efo/EFO_0800709 GCST90140389 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12193 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12193 measurement http://www.ebi.ac.uk/efo/EFO_0800710 GCST90140390 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12216 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90140391 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12221 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12221 measurement http://www.ebi.ac.uk/efo/EFO_0800711 GCST90140392 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12261 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12261 measurement http://www.ebi.ac.uk/efo/EFO_0021301 GCST90140393 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12262 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12262 measurement http://www.ebi.ac.uk/efo/EFO_0800712 GCST90140394 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12283 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12283 measurement http://www.ebi.ac.uk/efo/EFO_0800713 GCST90140395 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12306 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12306 measurement http://www.ebi.ac.uk/efo/EFO_0800714 GCST90140396 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12407 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90140397 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12410 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12410 measurement http://www.ebi.ac.uk/efo/EFO_0800715 GCST90140398 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12411 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12411 measurement http://www.ebi.ac.uk/efo/EFO_0800716 GCST90140399 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12456 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12456 measurement http://www.ebi.ac.uk/efo/EFO_0021311 GCST90140400 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12462 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12462 measurement http://www.ebi.ac.uk/efo/EFO_0800717 GCST90140401 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12524 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12524 measurement http://www.ebi.ac.uk/efo/EFO_0021314 GCST90140402 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12543 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12543 measurement http://www.ebi.ac.uk/efo/EFO_0800718 GCST90140403 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12544 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12544 measurement http://www.ebi.ac.uk/efo/EFO_0021315 GCST90140404 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12680 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90140405 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12689 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 X-12689 measurement http://www.ebi.ac.uk/efo/EFO_0800719 GCST90140406 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12707 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 X-12707 measurement http://www.ebi.ac.uk/efo/EFO_0800720 GCST90140408 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12713 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 X-12713 measurement http://www.ebi.ac.uk/efo/EFO_0800721 GCST90140409 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12714 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12714 measurement http://www.ebi.ac.uk/efo/EFO_0800722 GCST90140410 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12718 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12718 measurement http://www.ebi.ac.uk/efo/EFO_0800723 GCST90140411 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12726 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12726 measurement http://www.ebi.ac.uk/efo/EFO_0021326 GCST90140412 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. X-12729 levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90140413 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hydantoin-5-propionate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 hydantoin-5-propionate measurement http://www.ebi.ac.uk/efo/EFO_0800051 GCST90139464 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxyglutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-hydroxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800052 GCST90139465 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-carboxyglutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gamma-carboxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800053 GCST90139466 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. S-methylcysteine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 S-methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800054 GCST90139467 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Argininate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 argininate measurement http://www.ebi.ac.uk/efo/EFO_0800055 GCST90139468 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-oxoarginine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90139469 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-methyl-5-imidazoleacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90139470 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. S-methylcysteine sulfoxide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 S-methylcysteine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0800058 GCST90139471 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Carboxyethyl-gaba levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 carboxyethyl-GABA measurement http://www.ebi.ac.uk/efo/EFO_0800059 GCST90139472 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Beta-citrylglutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90139473 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6-methyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90139474 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Imidazole propionate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90139475 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lanthionine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 lanthionine measurement http://www.ebi.ac.uk/efo/EFO_0800063 GCST90139476 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylcarnosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 X-12244--N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0021299 GCST90139477 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-methyltaurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-methyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800064 GCST90139478 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-1-methylhistidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-acetyl-1-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800065 GCST90139479 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 6-oxopiperidine-2-carboxylate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 6-oxopiperidine-2-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800066 GCST90139480 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-delta-acetylornithine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90139481 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Acisoga levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90139482 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-formylanthranilic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-formylanthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0800069 GCST90139483 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N2,N5-diacetylornithine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N2,N5-diacetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800070 GCST90139484 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methoxytyramine sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90139485 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methionine sulfone levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90139486 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Fructosyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 fructosyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800073 GCST90139487 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyltaurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90139488 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Homocitrulline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90139414 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90139415 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indoleacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90139416 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-methylhistidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90139417 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isobutyrylcarnitine (c4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90139418 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indolepropionate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90139419 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyltyrosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90139420 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pro-hydroxy-pro levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90139421 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxy-2-ethylpropionate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90139422 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-methyl-4-imidazoleacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-methyl-4-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800015 GCST90139423 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Guanidinosuccinate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 guanidinosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800016 GCST90139424 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90139425 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyltryptophan levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N-acetyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800018 GCST90139426 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylphenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90139427 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylarginine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90139428 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylthreonine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90139429 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylisoleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800021 GCST90139430 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylhistidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90139431 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-hydroxyisovalerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90139432 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isovalerylcarnitine (C5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 isovalerylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800024 GCST90139433 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cysteine-glutathione disulfide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90139434 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isovalerylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 isovalerylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800025 GCST90139435 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methylbutyrylcarnitine (C5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-methylbutyrylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800026 GCST90139436 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90139437 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pyroglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST90139438 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxy-3-methylvalerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-hydroxy-3-methylvalerate measurement http://www.ebi.ac.uk/efo/EFO_0800027 GCST90139439 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylcitrulline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800028 GCST90139440 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isobutyrylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 isobutyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800029 GCST90139441 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glutarylcarnitine (c5-dc) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 glutarylcarnitine (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800030 GCST90139442 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Beta-hydroxyisovaleroylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 beta-hydroxyisovaleroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800031 GCST90139443 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tiglylcarnitine (C5:1-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90139444 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-aspartyl-glutamate (naag) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetyl-aspartyl-glutamate (NAAG) measurement http://www.ebi.ac.uk/efo/EFO_0800033 GCST90139445 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-ribosyl-imidazoleacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90139446 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indoleacetylglutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 indoleacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800035 GCST90139447 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6-acetyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90139448 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tryptophan betaine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90139449 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dimethylarginine (sdma + adma) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90139450 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylserine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90139451 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-methylproline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90139452 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-methylthioribose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-methylthioribose measurement http://www.ebi.ac.uk/efo/EFO_0800040 GCST90139453 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cysteine sulfinic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cysteine sulfinic acid measurement http://www.ebi.ac.uk/efo/EFO_0800041 GCST90139454 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. S-methylmethionine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 S-methylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800042 GCST90139455 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indole-3-carboxylate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 indole-3-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800043 GCST90139456 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-3-methylhistidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetyl-3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800044 GCST90139457 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-cadaverine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-acetyl-cadaverine measurement http://www.ebi.ac.uk/efo/EFO_0800045 GCST90139458 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-ketoglutaramate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 alpha-ketoglutaramate measurement http://www.ebi.ac.uk/efo/EFO_0800046 GCST90139459 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methylglutaconate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 3-methylglutaconate measurement http://www.ebi.ac.uk/efo/EFO_0800047 GCST90139460 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-(galactosylhydroxy)-L-lysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-(galactosylhydroxy)-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800048 GCST90139461 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cysteinylglycine disulfide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 cysteinylglycine disulfide measurement http://www.ebi.ac.uk/efo/EFO_0800049 GCST90139462 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Formiminoglutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 formiminoglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800050 GCST90139463 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Enterolactone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 enterolactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801029 GCST90140860 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90139389 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Xanthurenate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90139390 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methyl-2-oxovalerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90139391 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methionine sulfoxide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90139392 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methylhistidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90139393 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-hydroxylysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5-hydroxylysine measurement http://www.ebi.ac.uk/efo/EFO_0800002 GCST90139394 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-guanidinobutanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90139395 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Imidazole lactate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90139396 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Kynurenine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90139397 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylglutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90139398 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-alpha-acetylornithine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-alpha-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800006 GCST90139399 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gentisate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90139400 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-aminovalerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800008 GCST90139401 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indolelactate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90139402 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-indoxyl sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-Indoxylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0010985 GCST90139403 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-methyl-2-oxopentanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90139404 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-hydroxyisocaproate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90139405 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isovalerate (i5:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 isovalerate (i5:0) measurement http://www.ebi.ac.uk/efo/EFO_0800010 GCST90139406 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-methylguanidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-methylguanidine measurement http://www.ebi.ac.uk/efo/EFO_0800011 GCST90139407 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenyllactate (pla) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90139408 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylaspartate (naa) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylaspartate (NAA) measurement http://www.ebi.ac.uk/efo/EFO_0800012 GCST90139409 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cysteine s-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90139411 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methyl-2-oxobutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90139412 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Homoarginine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST90139413 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylkynurenine (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 N-acetylkynurenine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800083 GCST90139499 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. C-glycosyltryptophan levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90139500 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenol glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phenol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800084 GCST90139501 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxybutyrate/2-hydroxyisobutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxyisobutyrate measurement, 2-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010979, http://www.ebi.ac.uk/efo/EFO_0020999 GCST90139502 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-hydroxyindole sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800085 GCST90139504 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 7-hydroxyindole sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 7-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800086 GCST90139505 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methylserine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-methylserine measurement http://www.ebi.ac.uk/efo/EFO_0800087 GCST90139506 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Catechol glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 catechol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800088 GCST90139507 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indolepropionylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 indolepropionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800089 GCST90139508 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N,N,N-trimethyl-5-aminovalerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90139509 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (N(1) + N(8))-acetylspermidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 (N(1) + N(8))-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0800091 GCST90139510 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hydroxyasparagine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 hydroxyasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800092 GCST90139511 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-methylhydroxyproline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-methylhydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800093 GCST90139512 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N,n,n-trimethyl-alanylproline betaine (tmap) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N,N,N-trimethyl-alanylproline betaine (TMAP) measurement http://www.ebi.ac.uk/efo/EFO_0800094 GCST90139513 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-carbamoylvaline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-carbamoylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800095 GCST90139514 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 8-methoxykynurenate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 8-methoxykynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800096 GCST90139515 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-amino-2-piperidone levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90139516 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N,N-dimethylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90139517 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 6-bromotryptophan levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 6-bromotryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800099 GCST90139518 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6,N6-dimethyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90139519 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-carboxyethylphenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-carboxyethylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800101 GCST90139520 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-carboxyethyltyrosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-carboxyethyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0800102 GCST90139521 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-carboxyethylvaline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-carboxyethylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800103 GCST90139522 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-carboxyethylleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-carboxyethylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800104 GCST90139523 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-carboxyethylisoleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-carboxyethylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800105 GCST90139524 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-ethylcatechol sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3-ethylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801047 GCST90140887 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-ethylcatechol sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-ethylcatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801048 GCST90140888 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-acetylcatechol sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-acetylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801049 GCST90140889 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-acetylcatechol sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-acetylcatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801050 GCST90140890 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-hydroxy-2-methylpyridine sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801051 GCST90140899 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxy-2-methylpyridine sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801052 GCST90140900 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-hydroxymethyl-2-furoylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-hydroxymethyl-2-furoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801053 GCST90140901 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3,5-dichloro-2,6-dihydroxybenzoic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3,5-dichloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801054 GCST90140903 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (S)-a-amino-omega-caprolactam levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 (S)-a-amino-omega-caprolactam measurement http://www.ebi.ac.uk/efo/EFO_0801055 GCST90140904 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Vanillic acid glycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 vanillic acid glycine measurement http://www.ebi.ac.uk/efo/EFO_0801056 GCST90140905 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methoxyhydroquinone glucuronide (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-methoxyhydroquinone glucuronide (2) measurement http://www.ebi.ac.uk/efo/EFO_0801057 GCST90140906 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-bromo-5-chloro-2,6-dihydroxybenzoic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-bromo-5-chloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801058 GCST90140910 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-chlorobenzoic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-chlorobenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801059 GCST90140912 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-4-chlorophenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetyl-4-chlorophenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0801060 GCST90140913 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methoxyhydroquinone sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-methoxyhydroquinone sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801061 GCST90140915 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-methoxyhydroquinone sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-methoxyhydroquinone sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801062 GCST90140916 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methyl indole-3-acetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 methyl indole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0801063 GCST90140917 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyhippurate (salicylurate) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90140924 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-acetaminophen sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021156 GCST90140927 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gluconate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90140928 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phytanate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phytanate measurement http://www.ebi.ac.uk/efo/EFO_0801065 GCST90140929 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Salicylate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90140930 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cotinine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST90140931 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Caffeine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 caffeine metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007872 GCST90140932 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dopamine 3-o-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 dopamine 3-O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800082 GCST90139498 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methylglutarylcarnitine (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 3-methylglutarylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800074 GCST90139489 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-formylphenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-formylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800075 GCST90139490 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tyramine O-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90139491 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylhistamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-acetylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0800077 GCST90139493 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Vanillactate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 vanillactate measurement http://www.ebi.ac.uk/efo/EFO_0800078 GCST90139494 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. P-cresol glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90139495 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-methoxyphenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-methoxyphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800080 GCST90139496 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dopamine 4-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dopamine 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800081 GCST90139497 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyhippurate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxyhippurate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801030 GCST90140861 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of piperine metabolite C17H21NO3 (3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801031 GCST90140862 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of piperine metabolite C17H21NO3 (4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90140863 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronide of piperine metabolite C17H21NO3 (5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (5) measurement http://www.ebi.ac.uk/efo/EFO_0801033 GCST90140864 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sulfate of piperine metabolite C16H19NO3 (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90140865 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sulfate of piperine metabolite C16H19NO3 (3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90140866 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sulfate of piperine metabolite C18H21NO3 (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sulfate of piperine metabolite C18H21NO3 (1) measurement http://www.ebi.ac.uk/efo/EFO_0801036 GCST90140867 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sulfate of piperine metabolite C18H21NO3 (3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sulfate of piperine metabolite C18H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801037 GCST90140868 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-naphthol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-naphthol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801038 GCST90140869 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (2,4 or 2,5)-dimethylphenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 (2,4 or 2,5)-dimethylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801039 GCST90140870 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-ethylcatechol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90140871 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-allylcatechol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90140872 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyfluorene sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2-hydroxyfluorene sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801042 GCST90140873 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxypyridine glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxypyridine glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801043 GCST90140874 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihydrocaffeate sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dihydrocaffeate sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801044 GCST90140884 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-(methylthio)acetaminophen sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-(methylthio)acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801045 GCST90140885 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2,6-dihydroxybenzoic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90140886 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 6-hydroxyindole sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90140807 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Propyl 4-hydroxybenzoate sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 propyl 4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801005 GCST90140808 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Umbelliferone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 umbelliferone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801006 GCST90140809 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Daidzein sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 daidzein sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801007 GCST90140810 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,2,3-benzenetriol sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90140811 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methoxycatechol sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90140812 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methoxycatechol sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-methoxycatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801010 GCST90140813 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3,4-methyleneheptanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90140819 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Thioproline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90140825 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Caffeic acid sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 caffeic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801013 GCST90140830 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-acetamidobenzoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-acetamidobenzoate measurement http://www.ebi.ac.uk/efo/EFO_0801014 GCST90140832 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Naringenin 7-glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 naringenin 7-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801015 GCST90140834 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ferulylglycine (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ferulylglycine (1) measurement http://www.ebi.ac.uk/efo/EFO_0801016 GCST90140835 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ferulylglycine (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ferulylglycine (2) measurement http://www.ebi.ac.uk/efo/EFO_0801017 GCST90140836 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Perfluorooctanesulfonate (PFOS) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 perfluorooctanesulfonate (PFOS) measurement http://www.ebi.ac.uk/efo/EFO_0801018 GCST90140837 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ethyl alpha-glucopyranoside levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ethyl alpha-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801019 GCST90140844 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methylnaphthyl sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 methylnaphthyl sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801020 GCST90140849 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methylnaphthyl sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 methylnaphthyl sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801021 GCST90140850 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxystachydrine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxystachydrine measurement http://www.ebi.ac.uk/efo/EFO_0801022 GCST90140851 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Genistein sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 genistein sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801023 GCST90140852 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Perfluorooctanoate (PFOA) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 perfluorooctanoate (PFOA) measurement http://www.ebi.ac.uk/efo/EFO_0801024 GCST90140853 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-formylindole levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90140855 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihydroferulic acid sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dihydroferulic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801026 GCST90140856 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-indoleglyoxylic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 3-indoleglyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801027 GCST90140858 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ethyl beta-glucopyranoside levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90140859 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-allylphenol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90140711 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxycoumarin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-hydroxycoumarin measurement http://www.ebi.ac.uk/efo/EFO_0800959 GCST90140713 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyhippurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90140715 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ergothioneine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90140716 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 7-methylurate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 7-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0800961 GCST90140717 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cinnamoylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90140718 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2,3-dihydroxyisovalerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90140725 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90140728 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hydroxycotinine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 hydroxycotinine measurement http://www.ebi.ac.uk/efo/EFO_0800964 GCST90140729 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cotinine N-oxide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cotinine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0800965 GCST90140730 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-oxindole-3-acetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-oxindole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0800968 GCST90140733 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Solanidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 solanidine measurement http://www.ebi.ac.uk/efo/EFO_0800966 GCST90140735 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ethyl glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ethyl glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800967 GCST90140741 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-oxindole-3-acetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-oxindole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0800968 GCST90140743 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihydroferulate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dihydroferulate measurement http://www.ebi.ac.uk/efo/EFO_0800969 GCST90140744 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alliin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 alliin measurement http://www.ebi.ac.uk/efo/EFO_0800970 GCST90140751 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Mannonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 mannonate measurement http://www.ebi.ac.uk/efo/EFO_0800971 GCST90140752 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Histidine betaine (hercynine) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 histidine betaine (hercynine) measurement http://www.ebi.ac.uk/efo/EFO_0800972 GCST90140757 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methyl catechol sulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-methyl catechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800973 GCST90140758 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-methylcatechol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90140759 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methyl catechol sulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90140760 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyibuprofen levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxyibuprofen measurement http://www.ebi.ac.uk/efo/EFO_0800976 GCST90140761 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Carboxyibuprofen levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 carboxyibuprofen measurement http://www.ebi.ac.uk/efo/EFO_0800977 GCST90140762 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Guaiacol sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 guaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800978 GCST90140769 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dimethyl sulfone levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dimethyl sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800979 GCST90140771 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3alpha,17beta-diol disulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 5alpha-androstan-3alpha,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800287 GCST90139828 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800288 GCST90139829 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3beta,17alpha-diol disulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90139830 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3beta,17beta-diol monosulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 5alpha-androstan-3beta,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800290 GCST90139831 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800291 GCST90139832 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androstenediol (3alpha, 17alpha) monosulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 androstenediol (3alpha, 17alpha) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800292 GCST90139833 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androstenediol (3alpha, 17alpha) monosulfate (3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 androstenediol (3alpha, 17alpha) monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0800293 GCST90139834 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androstenediol (3beta,17beta) monosulfate (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 androstenediol (3beta,17beta) monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800294 GCST90139835 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androstenediol (3beta,17beta) monosulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 androstenediol (3beta,17beta) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800295 GCST90139836 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-docosahexaenoyl-GPE (22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-docosahexaenoyl-GPE (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800296 GCST90139837 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-docosahexaenoyl-GPE (22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2-docosahexaenoyl-GPE (22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800297 GCST90139838 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-docosapentaenoyl-GPC (22:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-docosapentaenoyl-GPC (22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800298 GCST90139839 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pregnenediol sulfate (C21H34O5S) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 pregnenediol sulfate (C21H34O5S) measurement http://www.ebi.ac.uk/efo/EFO_0800299 GCST90139840 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyglutarate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90139841 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139842 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoyl sphingomyelin (d18:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90139843 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 16a-hydroxy DHEA 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90139844 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 17alpha-hydroxypregnenolone 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 17alpha-hydroxypregnenolone 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800302 GCST90139845 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pregnenolone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 pregnenolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800303 GCST90139846 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-HEPE levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-HEPE measurement http://www.ebi.ac.uk/efo/EFO_0800304 GCST90139847 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Andro steroid monosulfate C19H28O6S (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90139849 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-margaroyl-GPE (17:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-margaroyl-GPE (17:0) measurement http://www.ebi.ac.uk/efo/EFO_0800306 GCST90139850 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-pentadecanoyl-GPC (15:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-pentadecanoyl-GPC (15:0) measurement http://www.ebi.ac.uk/efo/EFO_0800307 GCST90139851 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 13-HODE + 9-HODE levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 13-HODE + 9-HODE measurement http://www.ebi.ac.uk/efo/EFO_0800308 GCST90139852 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tridecenedioate (C13:1-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 tridecenedioate (C13:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800309 GCST90139853 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-cholesten-3-one levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-cholesten-3-one measurement http://www.ebi.ac.uk/efo/EFO_0800310 GCST90139854 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cis-4-decenoylcarnitine (C10:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 cis-4-decenoylcarnitine (C10:1) measurement http://www.ebi.ac.uk/efo/EFO_0800311 GCST90139855 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2s,3R-dihydroxybutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2s,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800312 GCST90139856 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (16 or 17)-methylstearate (a19:0 or i19:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 (16 or 17)-methylstearate (a19:0 or i19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800313 GCST90139857 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2R,3R-dihydroxybutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2R,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800314 GCST90139858 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isoursodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 isoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800315 GCST90139859 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxy-2-oxoglutaric acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90139860 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Androsterone glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90139861 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cis-4-decenoate (10:1n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 cis-4-decenoate (10:1n6) measurement http://www.ebi.ac.uk/efo/EFO_0800318 GCST90139862 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-meadoyl-GPC (20:3n9) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-meadoyl-GPC (20:3n9) measurement http://www.ebi.ac.uk/efo/EFO_0800319 GCST90139863 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-erucoyl-GPC (22:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-erucoyl-GPC (22:1) measurement http://www.ebi.ac.uk/efo/EFO_0800320 GCST90139864 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-adrenoyl-GPC (22:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-adrenoyl-GPC (22:4) measurement http://www.ebi.ac.uk/efo/EFO_0800321 GCST90139865 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-lignoceroyl-GPC (24:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-lignoceroyl-GPC (24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800322 GCST90139866 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-GPC (p-16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-(1-enyl-palmitoyl)-GPC (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800323 GCST90139867 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-oleoyl)-GPC (p-18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-oleoyl)-GPC (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800324 GCST90139868 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-GPC (p-18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-(1-enyl-stearoyl)-GPC (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800325 GCST90139869 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycoursodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90139870 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tauroursodeoxycholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 tauroursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800327 GCST90139871 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ursocholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 ursocholate measurement http://www.ebi.ac.uk/efo/EFO_0800328 GCST90139872 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (14 or 15)-methylpalmitate (a17:0 or i17:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 (14 or 15)-methylpalmitate (a17:0 or i17:0) measurement http://www.ebi.ac.uk/efo/EFO_0800329 GCST90139873 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Eicosanedioate (C20-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 eicosanedioate (C20-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800330 GCST90139874 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosadioate (C22-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 docosadioate (C22-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800331 GCST90139875 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoyl-linoleoyl-glycerol (18:1/18:2) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 oleoyl-linoleoyl-glycerol (18:1/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800332 GCST90139876 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoyl-linoleoyl-glycerol (18:1/18:2) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 oleoyl-linoleoyl-glycerol (18:1/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800333 GCST90139877 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-GPE (p-16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-palmitoyl)-GPE (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800334 GCST90139878 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-GPE (p-18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-stearoyl)-GPE (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800335 GCST90139879 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-stearoyl-GPI (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800336 GCST90139880 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-oleoyltaurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-oleoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800337 GCST90139881 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoylcarnitine (C18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90139882 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-palmitoyltaurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-palmitoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800339 GCST90139883 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-stearoyltaurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-stearoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800340 GCST90139884 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Trimethylamine n-oxide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90139885 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pregnanediol-3-glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90139886 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-palmitoylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-palmitoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800342 GCST90139887 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-stearoyl-GPE (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800343 GCST90139888 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (R)-3-hydroxybutyrylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 (R)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800344 GCST90139889 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Margaroylcarnitine (C17) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 margaroylcarnitine (C17) measurement http://www.ebi.ac.uk/efo/EFO_0800345 GCST90139890 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycohyocholate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glycohyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800346 GCST90139891 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxydecanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800347 GCST90139893 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3b-hydroxy-5-cholenoic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 3b-hydroxy-5-cholenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800348 GCST90139894 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-aminooctanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90139895 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-GPS (18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-stearoyl-GPS (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800350 GCST90139896 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139897 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139898 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyadipate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 3-hydroxyadipate measurement http://www.ebi.ac.uk/efo/EFO_0800351 GCST90139899 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-aminoheptanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90139900 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-eicosapentaenoyl-GPE (20:5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-eicosapentaenoyl-GPE (20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800353 GCST90139901 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linolenoyl-GPC (18:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-linolenoyl-GPC (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800354 GCST90139902 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-eicosapentaenoyl-GPC (20:5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-eicosapentaenoyl-GPC (20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800355 GCST90139903 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-eicosenoyl-GPC (20:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-eicosenoyl-GPC (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800356 GCST90139904 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-nonadecanoyl-GPC (19:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-nonadecanoyl-GPC (19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800357 GCST90139905 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-dihomo-linolenoyl-GPE (20:3n3 or 6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-dihomo-linolenoyl-GPE (20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800358 GCST90139906 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-oleoyl)-GPE (p-18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-oleoyl)-GPE (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800359 GCST90139907 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3alpha,17beta-diol 17-glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 5alpha-androstan-3alpha,17beta-diol 17-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800360 GCST90139908 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 11-ketoetiocholanolone glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 11-ketoetiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800361 GCST90139909 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Etiocholanolone glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90139910 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 17alpha-hydroxypregnanolone glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 17alpha-hydroxypregnanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800363 GCST90139911 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-docosapentaenoyl-GPC (22:5n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-docosapentaenoyl-GPC (22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800364 GCST90139912 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linolenoyl-GPE (18:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-linolenoyl-GPE (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800365 GCST90139913 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-GPG (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-oleoyl-GPG (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800366 GCST90139914 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-GPG (16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-GPG (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800367 GCST90139915 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-linoleoyltaurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-linoleoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800368 GCST90139916 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 9-hydroxystearate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 9-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0800369 GCST90139917 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/14:0, d18:1/14:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139918 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139919 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Octadecenedioylcarnitine (C18:1-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 octadecenedioylcarnitine (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800370 GCST90139920 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiota abundance (Lachnoanaerobaculum) in oral squamous cell carcinoma 144 individuals 67 individuals Affymetrix [165744] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90101804 Genome-wide genotyping array 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiota abundance (Kingella) in oral squamous cell carcinoma 144 individuals 67 individuals Affymetrix [165744] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90101805 Genome-wide genotyping array 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiota abundance (Parvimonas) in oral squamous cell carcinoma 144 individuals 67 individuals Affymetrix [165744] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90101806 Genome-wide genotyping array 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiota abundance (Aggregatibacter) in oral squamous cell carcinoma 144 individuals 67 individuals Affymetrix [165744] 0 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90101807 Genome-wide genotyping array 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiome alpha diversity (Chao1 index) in oral squamous cell carcinoma 144 individuals NA Affymetrix [165744] 2 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90204202 Genome-wide genotyping array 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiome alpha diversity (Shannon index) in oral squamous cell carcinoma 144 individuals NA Affymetrix [165744] 2 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90204203 Genome-wide genotyping array 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiome beta diversity (Euclidian distance) in oral squamous cell carcinoma 144 individuals NA Affymetrix [165744] 6 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90204204 Genome-wide genotyping array 2022-11-28 34875929 Yang SF 2021-12-07 J Dent Res www.ncbi.nlm.nih.gov/pubmed/34875929 Host Genetic Associations with Salivary Microbiome in Oral Cancer. Oral microbiome beta diversity (Bray-Curtis) in oral squamous cell carcinoma 144 individuals NA Affymetrix [165744] 12 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90204205 Genome-wide genotyping array 2022-11-17 36335192 Piga NN 2022-11-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36335192 Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK. Smoking initiation (ever vs never) 10,558 African ancestry individuals NA Illumina [14459454] (imputed) 7 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90091238 Genome-wide genotyping array 2022-11-17 36335192 Piga NN 2022-11-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36335192 Genetic insights into smoking behaviours in 10,558 men of African ancestry from continental Africa and the UK. Smoking cessation (current vs former) 4,257 African ancestry individuals NA Illumina [14057868] (imputed) 1 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90091239 Genome-wide genotyping array 2022-11-08 36093044 Mathieu S 2022-08-20 iScience www.ncbi.nlm.nih.gov/pubmed/36093044 Genetic association and Mendelian randomization for hypothyroidism highlight immune molecular mechanisms. Hypothyroidism 51,194 European ancestry cases, 443,383 European ancestry controls 17,002 cases, 178,141 controls Affymetrix, Illumina [10836150] (imputed) 69 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90204167 Genome-wide genotyping array 2022-10-26 36238604 van der Zanden LFM 2022-09-27 Front Pediatr www.ncbi.nlm.nih.gov/pubmed/36238604 Genome-wide association study in patients with posterior urethral valves. Posterior urethral valves 756 European ancestry cases, 4,823 European ancestry controls NA NR [5754208] (imputed) 15 posterior urethral valve http://purl.obolibrary.org/obo/MONDO_0019640 GCST90134327 Genome-wide genotyping array 2022-11-10 36282123 Thorolfsdottir RB 2021-05-01 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/36282123 Genetic insight into sick sinus syndrome. Sick sinus syndrome 6,189 European ancestry cases, 931,046 European ancestry controls 280 European ancestry cases, 69,141 European ancestry controls Affymetrix, Illumina [NR] (imputed) 6 sick sinus syndrome http://purl.obolibrary.org/obo/MONDO_0001823 GCST90225551 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Hypertension 91,620 European ancestry individuals NA NR [580000] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90225552 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Height 91,438 European ancestry individuals NA NR [580000] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90225553 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Waist circumference 91,476 European ancestry individuals NA NR [580000] 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90225554 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Hip circumference 91,469 European ancestry individuals NA NR [580000] 0 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90225555 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Waist-hip ratio 91,460 European ancestry individuals NA NR [580000] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90225556 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Systolic blood pressure 85,950 European ancestry individuals NA NR [580000] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90225557 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Diastolic blood pressure 85,951 European ancestry individuals NA NR [580000] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90225558 Genome-wide genotyping array 2022-11-09 36217425 Lin Z 2022-09-20 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36217425 Leveraging omics data to boost the power of genome-wide association studies. Body mass index 91,337 European ancestry individuals NA NR [580000] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90225559 Genome-wide genotyping array 2022-11-09 36187959 Guo H 2022-09-15 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/36187959 Identifying shared genetic loci between coronavirus disease 2019 and cardiovascular diseases based on cross-trait meta-analysis. COVID-19 or coronary artery disease (pleiotropy) up to 2,244 European ancestry critical COVID-19 cases, 60,801 European or uknown ancestry CAD cases, up to 128,820 European or unknown ancestry controls NA NR [4380210] 10 COVID-19, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90225531 Genome-wide genotyping array 2022-11-09 36187959 Guo H 2022-09-15 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/36187959 Identifying shared genetic loci between coronavirus disease 2019 and cardiovascular diseases based on cross-trait meta-analysis. COVID-19 or type 2 diabetes (pleiotropy) up to 2,244 European ancestry critical COVID-19 cases, 26,676 European ancestry T2D cases, up to 137,848 European ancestry controls NA NR [4380210] 3 type 2 diabetes mellitus, COVID-19 http://purl.obolibrary.org/obo/MONDO_0005148, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90225532 Genome-wide genotyping array 2022-11-09 36187959 Guo H 2022-09-15 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/36187959 Identifying shared genetic loci between coronavirus disease 2019 and cardiovascular diseases based on cross-trait meta-analysis. COVID-19 or hypertension (pleiotropy) up to 2,244 European ancestry critical COVID-19 cases, 99,665 European ancestry hypertension cases, up to 194,958 European ancestry controls NA NR [4380210] 21 hypertension, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000537, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90225533 Genome-wide genotyping array 2022-11-09 36187959 Guo H 2022-09-15 Front Microbiol www.ncbi.nlm.nih.gov/pubmed/36187959 Identifying shared genetic loci between coronavirus disease 2019 and cardiovascular diseases based on cross-trait meta-analysis. COVID-19 or obesity (pleiotropy) up to 2,244 European ancestry critical COVID-19 cases, 32,858 European ancestry obesity cases, up to 71,155 European ancestry controls NA NR [2380428] 5 COVID-19, obesity http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0001073 GCST90225534 Genome-wide genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Crohn's disease x smoking status (never vs ever smoking) interaction 10,856 cases, 4,887 controls NA Illumina [132890] 2 smoking status measurement, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90137949 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Ulcerative colitis x smoking status (never vs ever smoking) interaction 8,879 cases, 4,887 controls NA Illumina [132890] 1 smoking status measurement, ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000729 GCST90137950 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Inflammatory bowel disease x smoking status (never vs ever smoking) interaction 19,735 cases, 4,887 controls NA Illumina [132890] 1 smoking status measurement, inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90137951 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Crohn's disease x smoking status (never vs current smoking) interaction 10,856 cases, 4,887 controls NA Illumina [132890] 3 smoking status measurement, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90137952 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Ulcerative colitis x smoking status (never vs current smoking) interaction 8,879 cases, 4,887 controls NA Illumina [132890] 7 smoking status measurement, ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000729 GCST90137953 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Inflammatory bowel disease x smoking status (never vs current smoking) interaction 19,735 cases, 4,887 controls NA Illumina [132890] 2 smoking status measurement, inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90137954 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Crohn's disease x smoking status (never vs former smoking) interaction 10,856 cases, 4,887 controls NA Illumina [132890] 1 smoking status measurement, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90137955 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Ulcerative colitis x smoking status (never vs former smoking) interaction 8,879 cases, 4,887 controls NA Illumina [132890] 1 smoking status measurement, ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000729 GCST90137956 Targeted genotyping array 2022-09-27 28506689 Yadav P 2017-05-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/28506689 Genetic Factors Interact With Tobacco Smoke to Modify Risk for Inflammatory Bowel Disease in Humans and Mice. Inflammatory bowel disease x smoking status (never vs former smoking) interaction 19,735 cases, 4,887 controls NA Illumina [132890] 4 smoking status measurement, inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90137957 Targeted genotyping array 2022-10-28 36240095 Jaworek T 2022-08-31 Neurology www.ncbi.nlm.nih.gov/pubmed/36240095 Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke. Early-onset ischemic stroke 11,114 European ancestry cases, 435,540 European ancestry controls, 189 Admixed American ancestry cases, 948 Admixed American ancestry controls, 2,970 East Asian ancestry cases, 153,739 East Asian ancestry controls, 230 Afro-Caribbean cases, 968 Afro-Caribbean controls, 990 African ancestry cases, 3,199 African ancestry controls, 1,237 South Asian ancestry cases, 4,536 South Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 21 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90188370 Genome-wide genotyping array 2022-10-28 36240095 Jaworek T 2022-08-31 Neurology www.ncbi.nlm.nih.gov/pubmed/36240095 Contribution of Common Genetic Variants to Risk of Early Onset Ischemic Stroke. Early-onset ischemic stroke 11,114 European ancestry cases, 435,540 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 17 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90188371 Genome-wide genotyping array 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Octadecanedioylcarnitine (C18-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 octadecanedioylcarnitine (C18-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800371 GCST90139921 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 5alpha-androstan-3alpha,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800372 GCST90139922 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myristoleoylcarnitine (C14:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90139923 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-dihomo-linolenylglycerol (20:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-dihomo-linolenylglycerol (20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800374 GCST90139924 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pregnanolone/allopregnanolone sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 allopregnanolone sulfate measurement, pregnanolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801074, http://www.ebi.ac.uk/efo/EFO_0800375 GCST90139925 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139926 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139927 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/20:2, d18:2/20:1, d16:1/22:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139928 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Behenoyl sphingomyelin (d18:1/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 behenoyl sphingomyelin (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800376 GCST90139929 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139930 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/22:2, d18:2/22:1, d16:1/24:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139931 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lignoceroyl sphingomyelin (d18:1/24:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 lignoceroyl sphingomyelin (d18:1/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800377 GCST90139932 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d17:1/16:0, d18:1/15:0, d16:1/17:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139933 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyhexanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90139934 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3beta-hydroxy-5-cholestenoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 3beta-hydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800379 GCST90139935 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Adipoylcarnitine (C6-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 adipoylcarnitine (C6-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800380 GCST90139936 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nonanoylcarnitine (C9) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 nonanoylcarnitine (C9) measurement http://www.ebi.ac.uk/efo/EFO_0800381 GCST90139937 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Suberoylcarnitine (C8-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 suberoylcarnitine (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800382 GCST90139938 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Deoxycholic acid 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 deoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800383 GCST90139939 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycochenodeoxycholate 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 glycochenodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800384 GCST90139940 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycodeoxycholate 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 glycodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800385 GCST90139941 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurodeoxycholic acid 3-sulfate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 taurodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800386 GCST90139942 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoyl ethanolamide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90139943 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,2-dilinoleoyl-GPC (18:2/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1,2-dilinoleoyl-GPC (18:2/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800388 GCST90139944 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-oleoyl-gpc (18:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-stearoyl-2-oleoyl-GPC (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800389 GCST90139945 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800390 GCST90139946 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-docosahexaenoyl-gpc (16:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800391 GCST90139947 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-docosahexaenoyl-gpc (18:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800392 GCST90139948 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-oleoyl-GPC (p-18:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-stearoyl)-2-oleoyl-GPC (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800393 GCST90139949 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPC (p-18:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-(1-enyl-stearoyl)-2-arachidonoyl-GPC (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800394 GCST90139950 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-oleoyl-GPE (p-18:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800395 GCST90139951 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139952 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90139953 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleate/vaccenate (18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 oleate (18:1) measurement, vaccenate (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0801072, http://www.ebi.ac.uk/efo/EFO_0800397 GCST90139954 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoleoylglycerol (16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-palmitoleoylglycerol (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800398 GCST90139955 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-palmitoleoylglycerol (16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-palmitoleoylglycerol (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800399 GCST90139956 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 palmitoyl dihydrosphingomyelin (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800400 GCST90139957 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tricosanoyl sphingomyelin (d18:1/23:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tricosanoyl sphingomyelin (d18:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0800401 GCST90139958 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139959 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139960 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800402 GCST90139961 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800403 GCST90139962 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-linoleoyl-gpc (18:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90139963 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-linoleoyl-GPC (18:1/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-oleoyl-2-linoleoyl-GPC (18:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800405 GCST90139964 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-2-palmitoleoyl-GPC(16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800406 GCST90139965 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800407 GCST90139966 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-eicosapentaenoyl-GPC (16:0/20:5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-2-eicosapentaenoyl-GPC (16:0/20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800408 GCST90139967 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800409 GCST90139968 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800410 GCST90139969 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800411 GCST90139970 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-09-08 35803233 Wu X 2022-07-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35803233 Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis. Uterine leiomyoma or breast cancer (pleiotropy) 35,474 European ancestry UL cases, 133,384 European ancestry BC cases, 381,294 European ancestry controls NA NR [8170973] (imputed) 29 Uterine leiomyoma, breast carcinoma http://purl.obolibrary.org/obo/HP_0000131, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90134420 Genome-wide genotyping array 2022-09-08 35803233 Wu X 2022-07-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35803233 Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis. Uterine leiomyoma or ER positive breast cancer (pleiotropy) 35,474 European ancestry UL cases, 69,501 European ancestry ER+ve BC cases, 373,479 European ancestry controls NA NR [8175419] (imputed) 17 Uterine leiomyoma, estrogen-receptor positive breast cancer http://purl.obolibrary.org/obo/HP_0000131, http://www.ebi.ac.uk/efo/EFO_1000649 GCST90134421 Genome-wide genotyping array 2022-09-08 35803233 Wu X 2022-07-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35803233 Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis. Uterine leiomyoma or ER negative breast cancer (pleiotropy) 35,474 European ancestry UL cases, 21,468 European ancestry ER-ve BC cases, 373,479 European ancestry controls NA NR [8175424] (imputed) 14 Uterine leiomyoma, estrogen-receptor negative breast cancer http://purl.obolibrary.org/obo/HP_0000131, http://www.ebi.ac.uk/efo/EFO_1000650 GCST90134422 Genome-wide genotyping array 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearyl-GPC (O-18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-stearyl-GPC (O-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800460 GCST90140021 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-dihomo-linolenoyl-GPC (18:1/20:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-oleoyl-2-dihomo-linolenoyl-GPC (18:1/20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800461 GCST90140022 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-eicosapentaenoyl-GPC (18:1/20:5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-oleoyl-2-eicosapentaenoyl-GPC (18:1/20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800462 GCST90140023 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-meadoyl-GPC (18:0/20:3n9) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-stearoyl-2-meadoyl-GPC (18:0/20:3n9) measurement http://www.ebi.ac.uk/efo/EFO_0800463 GCST90140024 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800464 GCST90140025 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-myristoyl-GPC (p-16:0/14:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-(1-enyl-palmitoyl)-2-myristoyl-GPC (P-16:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800465 GCST90140026 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800466 GCST90140027 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphatidylcholine (16:0/22:5n3, 18:1/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 phosphatidylcholine (16:0/22:5n3, 18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800467 GCST90140028 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphatidylcholine (18:0/20:5, 16:0/22:5n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 phosphatidylcholine (18:0/20:5, 16:0/22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800468 GCST90140029 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-oleoyl-GPI (18:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-stearoyl-2-oleoyl-GPI (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800469 GCST90140030 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800470 GCST90140031 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-docosahexaenoyl-GPE (18:1/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-oleoyl-2-docosahexaenoyl-GPE (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800471 GCST90140032 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (p-18:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90140033 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-GPG (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-linoleoyl-GPG (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800472 GCST90140034 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoylcholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800473 GCST90140035 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycochenodeoxycholate glucuronide (1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90140036 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. (S)-3-hydroxybutyrylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 (S)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800475 GCST90140037 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800476 GCST90140038 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoylcholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 oleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800477 GCST90140039 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arachidonoylcholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 arachidonoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800478 GCST90140040 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Docosahexaenoylcholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 docosahexaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800479 GCST90140041 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoloelycholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitoloelycholine measurement http://www.ebi.ac.uk/efo/EFO_0800480 GCST90140042 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dihomo-linolenoyl-choline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 dihomo-linolenoyl-choline measurement http://www.ebi.ac.uk/efo/EFO_0800481 GCST90140043 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Eicosapentaenoylcholine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 eicosapentaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800482 GCST90140044 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800483 GCST90140045 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800412 GCST90139971 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800413 GCST90139972 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-palmitoleoyl-GPE (16:0/16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoyl-2-palmitoleoyl-GPE (16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800414 GCST90139973 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (p-18:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800415 GCST90139974 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPE (p-16:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPE (P-16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800416 GCST90139975 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (p-16:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800417 GCST90139976 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPE (p-18:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPE (P-18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800418 GCST90139977 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (p-16:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800419 GCST90139978 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-oleoyl-gpc (p-16:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800420 GCST90139979 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPC (p-16:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-(1-enyl-palmitoyl)-2-docosahexaenoyl-GPC (P-16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800421 GCST90139980 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (p-16:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800422 GCST90139981 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90139982 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPC (p-18:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-stearoyl)-2-docosahexaenoyl-GPC (P-18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800424 GCST90139983 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmityl-2-oleoyl-GPC (o-16:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmityl-2-oleoyl-GPC (O-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800425 GCST90139984 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmityl-2-arachidonoyl-GPC (o-16:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmityl-2-arachidonoyl-GPC (O-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800426 GCST90139985 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139986 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Behenoyl dihydrosphingomyelin (d18:0/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 behenoyl dihydrosphingomyelin (d18:0/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800427 GCST90139987 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingomyelin (d18:0/18:0, d19:0/17:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90139988 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-palmitoyl-sphinganine (d18:0/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90139989 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800429 GCST90139990 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-pentadecanoyl-2-linoleoyl-GPC (15:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-pentadecanoyl-2-linoleoyl-GPC (15:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800430 GCST90139991 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-margaroyl-2-oleoyl-GPC (17:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-margaroyl-2-oleoyl-GPC (17:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800431 GCST90139992 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-margaroyl-2-linoleoyl-GPC (17:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-margaroyl-2-linoleoyl-GPC (17:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800432 GCST90139993 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myristoyl dihydrosphingomyelin (d18:0/14:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 myristoyl dihydrosphingomyelin (d18:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800433 GCST90139994 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-dihomo-linolenoyl-GPC (18:0/20:3n3 or 6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-stearoyl-2-dihomo-linolenoyl-GPC (18:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800434 GCST90139995 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoyl-linoleoyl-glycerol (16:0/18:2) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 palmitoyl-linoleoyl-glycerol (16:0/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800435 GCST90139996 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoleoyl-oleoyl-glycerol (16:1/18:1) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitoleoyl-oleoyl-glycerol (16:1/18:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800436 GCST90139997 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoleoyl-oleoyl-glycerol (16:1/18:1) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitoleoyl-oleoyl-glycerol (16:1/18:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800437 GCST90139998 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoyl-linoleoyl-glycerol (16:0/18:2) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 palmitoyl-linoleoyl-glycerol (16:0/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800438 GCST90139999 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800439 GCST90140000 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (p-16:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800440 GCST90140001 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoleoyl-2-linoleoyl-GPC (16:1/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoleoyl-2-linoleoyl-GPC (16:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800441 GCST90140002 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-alpha-linolenoyl-GPC (16:0/18:3n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-2-alpha-linolenoyl-GPC (16:0/18:3n3) measurement http://www.ebi.ac.uk/efo/EFO_0800442 GCST90140003 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800443 GCST90140004 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-dihomo-linolenoyl-GPE (16:0/20:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-palmitoyl-2-dihomo-linolenoyl-GPE (16:0/20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800444 GCST90140005 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-GPA (18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-linoleoyl-GPA (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800445 GCST90140006 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-pentadecanoyl-2-arachidonoyl-GPC (15:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-pentadecanoyl-2-arachidonoyl-GPC (15:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800446 GCST90140007 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-pentadecanoyl-2-docosahexaenoyl-GPC (15:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-pentadecanoyl-2-docosahexaenoyl-GPC (15:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800447 GCST90140008 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-margaroyl-2-docosahexaenoyl-GPC (17:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-margaroyl-2-docosahexaenoyl-GPC (17:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800448 GCST90140009 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800449 GCST90140010 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800450 GCST90140011 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-stearoyl)-2-linoleoyl-GPC (p-18:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-stearoyl)-2-linoleoyl-GPC (P-18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800451 GCST90140012 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-myristoyl-2-linoleoyl-GPC (14:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1-myristoyl-2-linoleoyl-GPC (14:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800452 GCST90140013 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800453 GCST90140014 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-myristoyl-2-docosahexaenoyl-GPC (14:0/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 1-myristoyl-2-docosahexaenoyl-GPC (14:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800454 GCST90140015 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800455 GCST90140016 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-stearoyl-2-docosapentaenoyl-GPC (18:0/22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800456 GCST90140017 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-adrenoyl-GPC (16:0/22:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmitoyl-2-adrenoyl-GPC (16:0/22:4) measurement http://www.ebi.ac.uk/efo/EFO_0800457 GCST90140018 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoyl-2-meadoyl-GPC (16:0/20:3n9) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoyl-2-meadoyl-GPC (16:0/20:3n9) measurement http://www.ebi.ac.uk/efo/EFO_0800458 GCST90140019 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-stearoyl-2-adrenoyl-GPC (18:0/22:4) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-stearoyl-2-adrenoyl-GPC (18:0/22:4) measurement http://www.ebi.ac.uk/efo/EFO_0800459 GCST90140020 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800484 GCST90140046 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphatidylcholine (14:0/14:0, 16:0/12:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phosphatidylcholine (14:0/14:0, 16:0/12:0) measurement http://www.ebi.ac.uk/efo/EFO_0800485 GCST90140047 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphatidylcholine (15:0/18:1, 17:0/16:1, 16:0/17:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 phosphatidylcholine (15:0/18:1, 17:0/16:1, 16:0/17:1) measurement http://www.ebi.ac.uk/efo/EFO_0800486 GCST90140048 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-oleoyl-2-docosapentaenoyl-GPC (18:1/22:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 1-oleoyl-2-docosapentaenoyl-GPC (18:1/22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800487 GCST90140049 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phosphatidylcholine (18:0/20:2, 20:0/18:2) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 phosphatidylcholine (18:0/20:2, 20:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800488 GCST90140050 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-linoleoyl-2-docosapentaenyol-GPC (18:2/22:5n3) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-linoleoyl-2-docosapentaenyol-GPC (18:2/22:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800489 GCST90140051 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-(1-enyl-oleoyl)-2-docosahexaenoyl-GPE (p-18:1/22:6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-(1-enyl-oleoyl)-2-docosahexaenoyl-GPE (P-18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800490 GCST90140052 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hexadecadienoate (16:2n6) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 hexadecadienoate (16:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800491 GCST90140053 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-myristoyl-2-eicosapentaenoyl-GPC (14:0/20:5) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-myristoyl-2-eicosapentaenoyl-GPC (14:0/20:5) measurement http://www.ebi.ac.uk/efo/EFO_0800492 GCST90140054 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoleoylcarnitine (C16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitoleoylcarnitine (C16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800493 GCST90140055 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800494 GCST90140056 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoyl-oleoyl-glycerol (16:0/18:1) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitoyl-oleoyl-glycerol (16:0/18:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800495 GCST90140057 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoyl-oleoyl-glycerol (16:0/18:1) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 palmitoyl-oleoyl-glycerol (16:0/18:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800496 GCST90140058 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoyl-oleoyl-glycerol (18:1/18:1) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 oleoyl-oleoyl-glycerol (18:1/18:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800497 GCST90140059 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoyl-oleoyl-glycerol (18:1/18:1) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 oleoyl-oleoyl-glycerol (18:1/18:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800498 GCST90140060 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800499 GCST90140061 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800500 GCST90140062 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoyl-linolenoyl-glycerol (18:2/18:3) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 linoleoyl-linolenoyl-glycerol (18:2/18:3) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800501 GCST90140063 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoyl-docosahexaenoyl-glycerol (18:2/22:6) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 linoleoyl-docosahexaenoyl-glycerol (18:2/22:6) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800502 GCST90140064 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoyl-docosahexaenoyl-glycerol (18:2/22:6) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 linoleoyl-docosahexaenoyl-glycerol (18:2/22:6) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800503 GCST90140065 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Palmitoleoyl-linoleoyl-glycerol (16:1/18:2) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 palmitoleoyl-linoleoyl-glycerol (16:1/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800504 GCST90140066 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Diacylglycerol (14:0/18:1, 16:0/16:1) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 diacylglycerol (14:0/18:1, 16:0/16:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800505 GCST90140067 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Diacylglycerol (14:0/18:1, 16:0/16:1) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 diacylglycerol (14:0/18:1, 16:0/16:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800506 GCST90140068 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoyl-arachidonoyl-glycerol (18:1/20:4) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 oleoyl-arachidonoyl-glycerol (18:1/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800507 GCST90140069 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oleoyl-arachidonoyl-glycerol (18:1/20:4) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 oleoyl-arachidonoyl-glycerol (18:1/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800508 GCST90140070 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Diacylglycerol (16:1/18:2 [2], 16:0/18:3 [1]) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 diacylglycerol (16:1/18:2 [2], 16:0/18:3 [1]) measurement http://www.ebi.ac.uk/efo/EFO_0800509 GCST90140071 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Linoleoyl-linoleoyl-glycerol (18:2/18:2) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 linoleoyl-linoleoyl-glycerol (18:2/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800510 GCST90140072 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Stearoyl-arachidonoyl-glycerol (18:0/20:4) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 stearoyl-arachidonoyl-glycerol (18:0/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800511 GCST90140073 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Diacylglycerol (12:0/18:1, 14:0/16:1, 16:0/14:1) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 diacylglycerol (12:0/18:1, 14:0/16:1, 16:0/14:1) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800512 GCST90140074 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Diacylglycerol (12:0/18:1, 14:0/16:1, 16:0/14:1) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 diacylglycerol (12:0/18:1, 14:0/16:1, 16:0/14:1) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800513 GCST90140075 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmityl-GPE (O-16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 1-palmityl-GPE (O-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800514 GCST90140076 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1-palmityl-2-palmitoyl-GPC (O-16:0/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 1-palmityl-2-palmitoyl-GPC (O-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800515 GCST90140077 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-palmitoyl-sphingadienine (d18:2/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-palmitoyl-sphingadienine (d18:2/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800516 GCST90140078 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800517 GCST90140079 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lactosyl-N-behenoyl-sphingosine (d18:1/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 lactosyl-N-behenoyl-sphingosine (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800518 GCST90140080 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-behenoyl-sphingadienine (d18:2/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N-behenoyl-sphingadienine (d18:2/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800519 GCST90140081 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800520 GCST90140082 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-stearoyl-sphingadienine (d18:2/18:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-stearoyl-sphingadienine (d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800521 GCST90140083 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxybehenate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxybehenate measurement http://www.ebi.ac.uk/efo/EFO_0800522 GCST90140084 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxynervonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-hydroxynervonate measurement http://www.ebi.ac.uk/efo/EFO_0800523 GCST90140085 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-palmitoylserine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-palmitoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800524 GCST90140086 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-oleoylserine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-oleoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800525 GCST90140087 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sphingadienine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 sphingadienine measurement http://www.ebi.ac.uk/efo/EFO_0800526 GCST90140088 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myristoyl-linoleoyl-glycerol (14:0/18:2) [1] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 myristoyl-linoleoyl-glycerol (14:0/18:2) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800527 GCST90140089 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Myristoyl-linoleoyl-glycerol (14:0/18:2) [2] levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 myristoyl-linoleoyl-glycerol (14:0/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800528 GCST90140090 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hexadecasphingosine (d16:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 hexadecasphingosine (d16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800529 GCST90140091 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ceramide (d16:1/24:1, d18:1/22:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90140092 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycosyl ceramide (d16:1/24:1, d18:1/22:1) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 glycosyl ceramide (d16:1/24:1, d18:1/22:1) measurement http://www.ebi.ac.uk/efo/EFO_0800530 GCST90140093 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-palmitoyl-heptadecasphingosine (d17:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-palmitoyl-heptadecasphingosine (d17:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800531 GCST90140094 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ceramide (d18:1/14:0, d16:1/16:0) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90140095 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Creatine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90139550 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cys-gly, oxidized levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90139551 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Anthranilate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 anthranilate measurement http://www.ebi.ac.uk/efo/EFO_0800123 GCST90139552 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-methoxytyrosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90139553 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxyphenylacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 4-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800124 GCST90139554 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Beta-hydroxyisovalerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90139555 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6,n6,n6-trimethyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90139556 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylputrescine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90139557 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-formylmethionine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-formylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800128 GCST90139558 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. S-adenosylhomocysteine (SAH) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 S-adenosylhomocysteine measurement http://www.ebi.ac.uk/efo/EFO_0010531 GCST90139559 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methylsuccinate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90139560 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ethylmalonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90139561 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-methylthioadenosine (mta) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90139562 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arginine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90139563 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Argininosuccinate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 argininosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0010461 GCST90139564 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Aspartate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90139565 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxyphenylacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 2-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800131 GCST90139566 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-(4-hydroxyphenyl)lactate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90139567 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylpyruvate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 phenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800132 GCST90139568 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Creatinine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90139569 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cysteinylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90139570 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cystine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90139571 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cystathionine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90139572 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 6 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90139573 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Guanidinoacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90139574 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Betaine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90139601 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Cysteine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90139602 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Dimethylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90139603 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90139604 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tyrosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90139605 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Asparagine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90139606 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Kynurenate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90139607 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucuronate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90139608 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Maltotriose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 maltotriose measurement http://www.ebi.ac.uk/efo/EFO_0800142 GCST90139609 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ribitol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90139610 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 1,5-anhydroglucitol (1,5-ag) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90139611 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ribonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 ribonate measurement http://www.ebi.ac.uk/efo/EFO_0800144 GCST90139612 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Galactonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90139613 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Erythronate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90139614 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Mannitol/sorbitol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 mannitol measurement, sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0021027, http://www.ebi.ac.uk/efo/EFO_0010533 GCST90139615 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N6-carboxymethyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 N6-carboxymethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800146 GCST90139616 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arabonate/xylonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 xylonate measurement, arabonate measurement http://www.ebi.ac.uk/efo/EFO_0800147, http://www.ebi.ac.uk/efo/EFO_0801066 GCST90139617 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arabitol/xylitol levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 arabitol measurement, xylitol measurement http://www.ebi.ac.uk/efo/EFO_0800148, http://www.ebi.ac.uk/efo/EFO_0801067 GCST90139618 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylglucosamine/n-acetylgalactosamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-acetylgalactosamine measurement, N-acetylglucosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149, http://www.ebi.ac.uk/efo/EFO_0801068 GCST90139619 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ribulonate/xylulonate/lyxonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 xylulonate measurement, lyxonate measurement, ribulonate measurement http://www.ebi.ac.uk/efo/EFO_0801070, http://www.ebi.ac.uk/efo/EFO_0800150, http://www.ebi.ac.uk/efo/EFO_0801069 GCST90139620 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glycerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90139621 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylneuraminate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90139622 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylglucosaminylasparagine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 N-acetylglucosaminylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800151 GCST90139623 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-phosphoglycerate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90139624 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lactate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90139625 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Indoleacetoylcarnitine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 indoleacetoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800106 GCST90139525 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetyl-isoputreanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90139526 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-hydroxyindole glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-hydroxyindole glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800108 GCST90139527 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N2-acetyl,N6-methyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N2-acetyl,N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800109 GCST90139528 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-ketocaprylate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 4 2-ketocaprylate measurement http://www.ebi.ac.uk/efo/EFO_0800110 GCST90139529 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2,3-dihydroxy-5-methylthio-4-pentenoate (dmtpa) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90139530 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hydroxy-N6,N6,N6-trimethyllysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 hydroxy-N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800112 GCST90139531 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-hydroxy-4-(methylthio)butanoic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2-hydroxy-4-(methylthio)butanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800113 GCST90139532 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Trans-4-hydroxyproline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90139533 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-oxoproline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90139534 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Picolinate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 picolinate measurement http://www.ebi.ac.uk/efo/EFO_0800115 GCST90139535 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Sarcosine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90139536 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pipecolate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90139537 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90139538 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylmethionine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90139539 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylvaline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800117 GCST90139540 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Thyroxine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90139541 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 3-hydroxyisobutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90139542 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N-acetylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90139543 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Vanillylmandelate (VMA) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90139544 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-acetamidobutanoate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90139545 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-aminobutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90139546 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 4-hydroxyphenylpyruvate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90139547 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tigloylglycine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tigloylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800121 GCST90139548 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Homovanillate (hva) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 HVA measurement http://www.ebi.ac.uk/efo/EFO_0005131 GCST90139549 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. S-1-pyrroline-5-carboxylate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90139575 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Histidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90139577 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Hypotaurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90139578 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Isoleucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90139579 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-aminoadipate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0800137 GCST90139580 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Citrulline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90139581 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Leucine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90139582 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Lysine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 3 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90139583 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Methionine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90139584 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Ornithine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90139585 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Phenylalanine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90139586 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Proline levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90139587 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Spermidine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90139588 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Serine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 5 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90139589 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Serotonin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90139590 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Taurine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90139591 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Urea levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90139592 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Trans-urocanate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 trans-urocanate measurement http://www.ebi.ac.uk/efo/EFO_0800138 GCST90139593 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glutamate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90139594 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glutamine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90139595 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Threonine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90139596 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Tryptophan levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90139597 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Valine levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90139598 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 5-hydroxyindoleacetate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 5-hydroxyindoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800139 GCST90139599 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-ketobutyrate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 alpha-ketobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800140 GCST90139600 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Glucose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90139626 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Mannose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90139627 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pyruvate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90139628 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Xylose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 xylose measurement http://www.ebi.ac.uk/efo/EFO_0800153 GCST90139629 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Arabinose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 arabinose measurement http://www.ebi.ac.uk/efo/EFO_0021030 GCST90139630 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Fructose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90139631 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Maltose levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 Maltose measurement http://www.ebi.ac.uk/efo/EFO_0021649 GCST90139632 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Oxalate (ethanedioate) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90139633 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Threonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90139634 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Trigonelline (n'-methylnicotinate) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90139635 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Pyridoxate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90139636 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. I-urobilinogen levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 I-urobilinogen measurement http://www.ebi.ac.uk/efo/EFO_0800155 GCST90139637 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nicotinamide riboside levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 nicotinamide riboside measurement http://www.ebi.ac.uk/efo/EFO_0800156 GCST90139638 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Nicotinate ribonucleoside levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 nicotinate ribonucleoside measurement http://www.ebi.ac.uk/efo/EFO_0800157 GCST90139639 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Heme levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 heme measurement http://www.ebi.ac.uk/efo/EFO_0800158 GCST90139640 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. N1-methyl-2-pyridone-5-carboxamide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90139642 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gulonate levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90139643 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Bilirubin (E,E) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90139644 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Bilirubin (E,Z or Z,E) levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90139645 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Beta-cryptoxanthin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 cryptoxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007897 GCST90139646 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Gamma-CEHC levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90139647 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. L-urobilin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 1 L-urobilin measurement http://www.ebi.ac.uk/efo/EFO_0800161 GCST90139648 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Astaxanthin levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 astaxanthin measurement http://www.ebi.ac.uk/efo/EFO_0800162 GCST90139649 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. Alpha-CEHC glucuronide levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 0 alpha-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800163 GCST90139650 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-14 35347128 Yin X 2022-03-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35347128 Genome-wide association studies of metabolites in Finnish men identify disease-relevant loci. 2-o-methylascorbic acid levels 6,136 Finnish ancestry individuals NA NR [16000000] (imputed) 2 2-O-methylascorbic acid measurement http://www.ebi.ac.uk/efo/EFO_0800164 GCST90139651 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Anxiety x environmental factor score interaction 32,228 White British ancestry males NA NR [NR] (imputed) 1 anxiety disorder, environmental factor http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102445 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Depression (PHQ-9 score) x environmental factor score interaction 38,507 White British ancestry females NA NR [NR] (imputed) 1 unipolar depression, environmental factor http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102446 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Depression (PHQ-9 score) x environmental factor score interaction 35,121 White British ancestry males NA NR [NR] (imputed) 1 unipolar depression, environmental factor http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102447 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Depression x environmental factor score interaction 38,164 White British ancestry females NA NR [NR] (imputed) 3 unipolar depression, environmental factor http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102448 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Depression x environmental factor score interaction 34,391 White British ancestry males NA NR [NR] (imputed) 0 unipolar depression, environmental factor http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102449 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Self-harm x environmental factor score interaction 38,954 White British ancestry females NA NR [NR] (imputed) 0 Self-injurious behavior, environmental factor http://purl.obolibrary.org/obo/HP_0100716, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102450 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Self-harm x environmental factor score interaction 35,528 White British ancestry males NA NR [NR] (imputed) 0 Self-injurious behavior, environmental factor http://purl.obolibrary.org/obo/HP_0100716, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102451 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Anxiety (GAD-7 score) x environmental factor score interaction 38,670 White British ancestry females NA NR [NR] (imputed) 1 generalized anxiety disorder, environmental factor http://www.ebi.ac.uk/efo/EFO_1001892, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102442 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Anxiety (GAD-7 score) x environmental factor score interaction 35,268 White British ancestry males NA NR [NR] (imputed) 0 generalized anxiety disorder, environmental factor http://www.ebi.ac.uk/efo/EFO_1001892, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102443 Genome-wide genotyping array 2022-11-11 35026594 Li C 2022-01-05 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/35026594 A multi-environments-gene interaction study of anxiety, depression and self-harm in the UK Biobank cohort. Anxiety x environmental factor score interaction 33,813 White British ancestry females NA NR [NR] (imputed) 1 anxiety disorder, environmental factor http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0000469 GCST90102444 Genome-wide genotyping array 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Glycine levels 7,142 European ancestry individuals NA NR [NR] 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90179192 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Triglyceride levels in large HDL 7,142 European ancestry individuals NA NR [NR] 1 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179193 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Triglyceride levels in medium HDL 7,142 European ancestry individuals NA NR [NR] 2 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179194 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Free cholesterol levels in IDL 7,142 European ancestry individuals NA NR [NR] 2 free cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90179195 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Triglyceride levels in small VLDL 7,142 European ancestry individuals NA NR [NR] 2 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90179196 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Tyrosine levels 7,142 European ancestry individuals NA NR [NR] 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90179197 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Monounsaturated fatty acid levels 7,142 European ancestry individuals NA NR [NR] 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90179198 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. High-density lipoprotein 2 cholesterol levels 7,142 European ancestry individuals NA NR [NR] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179199 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Degree of unsaturation 7,142 European ancestry individuals NA NR [NR] 4 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90179200 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Histidine levels 7,142 European ancestry individuals NA NR [NR] 2 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90179201 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Triglycerides to total lipids ratio in very small VLDL 7,142 European ancestry individuals NA NR [NR] 1 triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90179202 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Docosahexaenoic acid levels 7,142 European ancestry individuals NA NR [NR] 1 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90179203 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. High-density lipoprotein 3 cholesterol levels 7,142 European ancestry individuals NA NR [NR] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179204 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Glutamine levels 7,142 European ancestry individuals NA NR [NR] 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90179205 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Cholesterol to total lipids ratio in small LDL 7,142 European ancestry individuals NA NR [NR] 2 cholesterol:total lipids ratio, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90179206 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Cholesteryl esters to total lipids ratio in small LDL 7,142 European ancestry individuals NA NR [NR] 3 cholesterol:total lipids ratio, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90179207 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Triglyceride levels 7,142 European ancestry individuals NA NR [NR] 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90179208 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Cholesteryl ester levels in very large VLDL 7,142 European ancestry individuals NA NR [NR] 1 cholesteryl ester measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90179209 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Apolipoprotein B levels 7,142 European ancestry individuals NA NR [NR] 1 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90179210 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Phospholipids to total lipids ratio in small LDL 7,142 European ancestry individuals NA NR [NR] 2 low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90179211 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. Phospholipids to total lipids ratio in large HDL 7,142 European ancestry individuals NA NR [NR] 2 phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020946, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179212 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 32150548 Riveros-Mckay F 2020-03-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32150548 The influence of rare variants in circulating metabolic biomarkers. HDL cholesterol levels 7,142 European ancestry individuals NA NR [NR] 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179213 Genome-wide sequencing, Exome-wide sequencing 2022-11-17 36281732 Sumpter NA 2022-10-25 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36281732 Association of Gout Polygenic Risk Score with Age at Disease Onset and Tophaceous Disease in European and Polynesian Men with Gout. Gout 7,131 European ancestry cases, 325,239 European ancestry controls NA Affymetrix [27287012] (imputed) 19 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90239691 Genome-wide genotyping array 2022-11-03 34934334 Lim ZW 2021-12-14 J Inflamm Res www.ncbi.nlm.nih.gov/pubmed/34934334 Polymorphism rs10105606 of LPL as a Novel Risk Factor for Microalbuminuria. Microalbuminuria 1,325 Han Chinese ancestry individuals NA Affymetrix [653291] 7 Moderate albuminuria http://purl.obolibrary.org/obo/HP_0012594 GCST90102287 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (2df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093218 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (2df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 7 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093168 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (2df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093169 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (2df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093170 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (2df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 10 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093171 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (2df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093172 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (2df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093173 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (2df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093174 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (2df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093222 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (2df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 9 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093177 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (2df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093178 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (1df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093179 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (1df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093180 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (2df test) NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093226 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (1df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093228 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (1df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093186 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (1df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 3 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093187 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (1df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093188 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (1df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093189 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (1df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093190 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (2df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093191 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (2df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093192 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093143 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (2df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 2 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093144 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (2df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 2 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093145 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093146 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (2df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 1 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093147 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (2df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093148 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093149 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (2df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 3 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093150 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (2df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 3 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093151 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093152 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (2df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 4 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093153 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (2df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 2 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093154 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093155 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (1df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 3 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093156 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (1df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 4 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093157 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093158 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (1df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 1 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093159 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (1df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093160 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093161 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (1df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 3 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093162 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (1df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 4 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093163 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals 2,527 African American individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093164 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (1df test) 14,597 African American individuals 3,070 African American individuals Affymetrix, Illumina [NR] (imputed) 1 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093165 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (1df test) 14,923 African American individuals 1,484 African American individuals Affymetrix, Illumina [NR] (imputed) 1 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093166 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (2df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093167 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (2df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093193 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (2df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093194 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (2df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093195 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (2df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093196 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (2df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093197 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (2df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093198 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (2df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093199 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (2df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093200 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (2df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093201 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (2df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093202 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (1df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093203 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (1df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093204 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (1df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093205 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (1df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093206 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (1df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093207 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (1df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093208 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (1df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093209 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (1df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093210 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (1df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093211 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (1df test) 747 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093212 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (1df test) 2,592 Asian ancestry individuals 3,458 East Asian ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093213 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (1df test) 749 Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093214 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (2df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093215 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (2df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093216 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (2df test) NA Affymetrix, Illumina [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093217 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (2df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093219 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (2df test) NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093220 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (2df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093221 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (2df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093175 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (2df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093176 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (2df test) NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093223 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (2df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093224 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (2df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093225 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (1df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093181 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (1df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093182 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (1df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093227 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (1df test) 43,335 European ancestry individuals 42,700 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093183 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (1df test) 24,943 European ancestry individuals 17,265 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093184 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (1df test) 12,800 European ancestry individuals 21,322 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093185 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (1df test) NA Affymetrix, Illumina [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093229 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (1df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093230 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (1df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093231 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (1df test) NA Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093232 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (1df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093233 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (1df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093234 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (1df test) NA Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093235 Genome-wide genotyping array 2022-08-30 35647563 Kingston H 2022-05-12 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35647563 Accounting for population structure in genetic studies of cystic fibrosis. CFTR mutation F508del heterozygosity in cystic fibrosis 90 African ancestry individuals, 196 Native American ancestry individuals, 5 East Asian ancestry individuals, 4,638 European ancestry individuals, 10 South Asian ancestry individuals NA Illumina [5843159] 10 CFTR mutation carrier status http://www.ebi.ac.uk/efo/EFO_0021794 GCST90132191 Genome-wide sequencing 2022-08-30 35647563 Kingston H 2022-05-12 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35647563 Accounting for population structure in genetic studies of cystic fibrosis. CFTR mutation F508del heterozygosity in cystic fibrosis (PC-adjusted model) 90 African ancestry individuals, 196 Native American ancestry individuals, 5 East Asian ancestry individuals, 4,638 European ancestry individuals, 10 South Asian ancestry individuals NA Illumina [5843159] 6 CFTR mutation carrier status http://www.ebi.ac.uk/efo/EFO_0021794 GCST90132192 Genome-wide sequencing 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (2df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 1 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093243 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (2df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093244 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (2df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093245 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (2df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093246 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (2df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 0 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093247 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (2df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093248 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (2df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 0 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093249 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (2df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093250 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (1df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093251 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (1df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 0 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093252 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (1df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093253 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (1df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093254 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (1df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 0 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093255 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (1df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093256 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (1df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093257 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (1df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093258 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (1df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 0 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093259 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (1df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093260 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (1df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 0 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093261 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (1df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093262 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093263 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (2df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 17 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093264 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (2df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 1 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093265 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093266 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (2df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 18 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093267 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (2df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 4 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093268 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 3 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093269 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (2df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093270 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (2df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 4 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093271 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (2df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093272 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (2df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 12 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093273 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (2df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 4 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093274 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093275 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (1df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 1 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093276 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (1df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093277 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093278 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x depressive symptoms interaction (1df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093279 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x low social support interaction (1df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 diastolic blood pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093280 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 3 pulse pressure measurement, anxiety http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093281 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x depressive symptoms interaction (1df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, unipolar depression http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093282 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Pulse pressure x low social support interaction (1df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 pulse pressure measurement, social deprivation http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093283 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (1df test) 2,433 African American individuals, 12,800 European ancestry individuals, 747 Asian ancestry individuals, 4,883 Hispanic individuals 2,527 African American individuals, 21,322 European ancestry individuals, 11,810 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093284 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (1df test) 14,597 African American individuals, 43,335 European ancestry individuals, 2,592 Asian ancestry individuals, 7,926 Hispanic individuals 3,070 African American individuals, 42,700 European ancestry individuals, 3,458 East Asian ancestry individuals, 11,818 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 2 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093285 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (1df test) 14,923 African American individuals, 24,943 European ancestry individuals, 749 Asian ancestry individuals, 4,425 Hispanic individuals 1,484 African American individuals, 17,265 European ancestry individuals, 3,949 Hispanic individuals Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093286 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x anxiety symptoms interaction (1df test) 3,477 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093236 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x depressive symptoms interaction (1df test) 3,499 Brazilian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, unipolar depression http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90093237 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Mean arterial pressure x low social support interaction (1df test) NA Affymetrix, Illumina [NR] (imputed) 0 mean arterial pressure, social deprivation http://www.ebi.ac.uk/efo/EFO_0006340, http://www.ebi.ac.uk/efo/EFO_0009696 GCST90093238 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x anxiety symptoms interaction (2df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 systolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093239 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x depressive symptoms interaction (2df test) 4,427 Hispanic individuals 11,818 Hispanic individuals Affymetrix [NR] (imputed) 0 unipolar depression, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093240 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Systolic blood pressure x low social support interaction (2df test) 4,425 Hispanic individuals 3,949 Hispanic individuals Affymetrix [NR] (imputed) 1 social deprivation, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009696, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90093241 Genome-wide genotyping array 2023-05-10 34734193 Sun D 2020-10-31 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34734193 Multi-Ancestry Genome-wide Association Study Accounting for Gene-Psychosocial Factor Interactions Identifies Novel Loci for Blood Pressure Traits. Diastolic blood pressure x anxiety symptoms interaction (2df test) 1,406 Hispanic individuals 11,810 Hispanic individuals Affymetrix [NR] (imputed) 0 diastolic blood pressure, anxiety http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90093242 Genome-wide genotyping array 2022-11-25 35220425 Pervjakova N 2022-02-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35220425 Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes. Gestational diabetes mellitus 91 African American cases, up to 985 African American controls, 867 East Asian ancestry cases, up to 2,984 East Asian ancestry controls, 3,780 European ancestry cases, up to 344,902 European ancestry controls, 174 Hispanic American cases, up to 619 Hispanic American controls, 573 South Asian ancestry cases, up to 3,761 South Asian ancestry controls NA Affymetrix, Illumina [7791032] (imputed) 8 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST90239750 Genome-wide genotyping array 2022-11-24 23468642 Kiefer AK 2013-02-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23468642 Genome-wide analysis points to roles for extracellular matrix remodeling, the visual cycle, and neuronal development in myopia. Myopia (age of diagnosis) 25,999 European ancestry cases, 19,772 European ancestry controls 1,488 cases, 6,835 controls Illumina [7087609] (imputed) 0 age of onset of myopia http://purl.obolibrary.org/obo/OBA_2001030 GCST90239747 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DERM level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90225585 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PCSK9 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 PCSK9 protein measurement http://www.ebi.ac.uk/efo/EFO_0006899 GCST90225586 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Caspase-10 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 caspase-10 measurement http://www.ebi.ac.uk/efo/EFO_0020239 GCST90225587 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sLeptin R level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90225588 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SLAF7 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90225589 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. N-terminal pro-BNP level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 N-terminal pro-BNP measurement http://www.ebi.ac.uk/efo/EFO_0022014 GCST90225590 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 sRII level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90225591 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CXCL16, soluble level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90225592 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sFRP-3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90225593 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 sRI level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90225594 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Granulysin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90225595 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TFPI level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90225596 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-18 Ra level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90225597 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PPAC level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90225598 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NAGK level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 N-acetyl-D-glucosamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0008239 GCST90225599 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 R4 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 interleukin 1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008168 GCST90225600 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SLPI level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 antileukoproteinase measurement http://www.ebi.ac.uk/efo/EFO_0020154 GCST90225601 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Collectin Kidney 1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90225602 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ASM3A level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90225603 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CAPG level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 macrophage-capping protein measurement http://www.ebi.ac.uk/efo/EFO_0020549 GCST90225604 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TSG-6 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor-inducible gene 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0008311 GCST90225605 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FAM3D level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90225606 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. 6Ckine level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-C motif chemokine 21 measurement http://www.ebi.ac.uk/efo/EFO_0008048 GCST90225607 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MCP-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-C motif chemokine 2 measurement http://www.ebi.ac.uk/efo/EFO_0021961 GCST90225608 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 R AcP level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 1 Receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008167 GCST90225609 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. LAG-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 C-C motif chemokine 4-like measurement http://www.ebi.ac.uk/efo/EFO_0021848 GCST90225610 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Endothelin-converting enzyme 1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90225611 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MSP level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 9 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90225612 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TXD12 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 6 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90225613 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Nr-CAM level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 neuronal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020602 GCST90225614 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cripto level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 10 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90225615 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CREL1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 cysteine-rich with EGF-like domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021870 GCST90225616 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Osteopontin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 osteopontin measurement http://www.ebi.ac.uk/efo/EFO_0021776 GCST90225617 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IDUA level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90225618 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ASAHL level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 5 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90225619 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BSP level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 bone sialoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020190 GCST90225620 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HGFA level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 hepatocyte growth factor activator measurement http://www.ebi.ac.uk/efo/EFO_0008152 GCST90225621 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Prekallikrein level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 plasma kallikrein measurement http://www.ebi.ac.uk/efo/EFO_0008260 GCST90225622 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BST1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90225623 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CBPE level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 carboxypeptidase e measurement http://www.ebi.ac.uk/efo/EFO_0020234 GCST90225624 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. EGF level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90225625 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Growth hormone receptor level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 growth hormone receptor measurement http://www.ebi.ac.uk/efo/EFO_0020426 GCST90225626 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HPLN1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 hyaluronan and proteoglycan link protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020459 GCST90225627 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TSP4 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 thrombospondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020771 GCST90225628 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PDGF Rb level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90225629 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Endocan level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 endothelial cell-specific molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010912 GCST90225630 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ARTS1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90225631 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TIMD3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90225632 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-9 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008192 GCST90225633 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BCL6 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 B-cell lymphoma 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0021933 GCST90225634 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GPNMB level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90225660 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Semaphorin 3E level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90225661 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HSP 60 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 60 kda heat shock protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020121 GCST90225662 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin B level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90225663 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TNFSF15 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90225664 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ATS13 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90225665 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CD30 Ligand level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90225666 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sE-Selectin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90225667 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DPP2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90225668 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TLR4:MD-2 complex level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90225669 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Tenascin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90225670 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Gelsolin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 gelsolin measurement http://www.ebi.ac.uk/efo/EFO_0020402 GCST90225671 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. B7-H1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90225672 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FSH level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90225673 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ASAH2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90225674 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ARMEL level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90225675 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cyclophilin F level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 peptidyl-prolyl cis-trans isomerase F, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020627 GCST90225676 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Fas, soluble level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90225677 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Testican-2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 testican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020766 GCST90225678 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NRP1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 neuropilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020603 GCST90225679 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. 3HAO level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 3-hydroxyanthranilate 3,4-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0021862 GCST90225680 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ERBB3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 receptor tyrosine-protein kinase erbb-3 measurement http://www.ebi.ac.uk/efo/EFO_0020701 GCST90225681 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Layilin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 layilin measurement http://www.ebi.ac.uk/efo/EFO_0020529 GCST90225682 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FGF-19 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90225683 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cystatin M level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90225684 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1F6 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 23 interleukin-36 alpha measurement http://www.ebi.ac.uk/efo/EFO_0021851 GCST90225635 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C4b level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 12 complement C4b measurement http://www.ebi.ac.uk/efo/EFO_0008092 GCST90225636 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ULBP-3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 NKG2-D ligand 3 measurement http://www.ebi.ac.uk/efo/EFO_0020611 GCST90225637 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Siglec-3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90225638 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. granzyme A level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90225639 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MDC level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90225640 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GNS level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90225641 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. LY86 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 lymphocyte antigen 86 measurement http://www.ebi.ac.uk/efo/EFO_0020541 GCST90225642 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SLAF5 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 5 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90225643 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IGF-II receptor level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90225644 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MFRP level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 12 membrane frizzled-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020563 GCST90225645 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Factor B level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 complement factor B measurement http://www.ebi.ac.uk/efo/EFO_0008096 GCST90225646 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FGF7 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90225647 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NCC27 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 chloride intracellular channel protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020256 GCST90225648 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PAFAH level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 platelet-activating factor acetylhydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020647 GCST90225649 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MICB level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 21 MHC class I polypeptide-related sequence B measurement http://www.ebi.ac.uk/efo/EFO_0008234 GCST90225650 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DLL1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90225651 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ERBB1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90225652 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HGF level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90225653 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NADPH-P450 Oxidoreductase level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 NADPH--cytochrome P450 reductase measurement http://www.ebi.ac.uk/efo/EFO_0008242 GCST90225654 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BAFF level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor ligand superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020793 GCST90225655 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TIG2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 retinoic acid receptor responder protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008274 GCST90225656 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. EphA1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 ephrin type-A receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008123 GCST90225657 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PYY level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 peptide yy measurement http://www.ebi.ac.uk/efo/EFO_0020623 GCST90225658 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PUR8 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 adenylosuccinate lyase measurement http://www.ebi.ac.uk/efo/EFO_0020130 GCST90225659 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Osteocalcin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90225560 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. REG4 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 regenerating islet-derived protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021921 GCST90225561 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. YKL-40 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90225562 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Hemopexin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 7 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90225563 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sTie-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 tyrosine-protein kinase receptor Tie-1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008312 GCST90225564 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin S level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 8 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90225565 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Nidogen level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 nidogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008249 GCST90225566 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PIGR level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90225567 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CD5L level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 CD5 antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0020248 GCST90225568 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CNTN2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90225569 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FCG2B level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 low affinity immunoglobulin gamma Fc region receptor II-b measurement http://www.ebi.ac.uk/efo/EFO_0021970 GCST90225570 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. LRP8 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 low-density lipoprotein receptor-related protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0020538 GCST90225571 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ECM1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008126 GCST90225572 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. LYNB level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 tyrosine-protein kinase LYN, isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020828 GCST90225573 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CAMK1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90225574 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Chitotriosidase-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90225575 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MMEL2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 membrane metallo-endopeptidase-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020564 GCST90225576 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. complement factor H-related 5 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90225577 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-6 sRa level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90225578 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. P-Selectin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90225579 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. 6-Phosphogluconate dehydrogenase level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 6-phosphogluconate dehydrogenase, decarboxylating measurement http://www.ebi.ac.uk/efo/EFO_0020120 GCST90225580 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. AK1A1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 5 alcohol dehydrogenase [NADP(+)] measurement http://www.ebi.ac.uk/efo/EFO_0021977 GCST90225581 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sL-Selectin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90225582 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Coagulation Factor V level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST90225583 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Galectin-8 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 galectin-8 measurement http://www.ebi.ac.uk/efo/EFO_0020399 GCST90225584 Genome-wide genotyping array 2022-11-07 36260985 Nethander M 2022-10-01 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36260985 Assessment of the genetic and clinical determinants of hip fracture risk: Genome-wide association and Mendelian randomization study. Hip fracture 11,516 European ancestry cases, 723,838 European ancestry controls NA Affymetrix, Illumina [9457767] (imputed) 5 hip fracture http://www.ebi.ac.uk/efo/EFO_0003964 GCST90161240 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Spondin-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90225685 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PCSK7 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90225686 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C1-Esterase Inhibitor level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90225687 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CDON level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 cell adhesion molecule-related/down-regulated by oncogenes measurement http://www.ebi.ac.uk/efo/EFO_0008079 GCST90225688 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Glutathione S-transferase Pi level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 7 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90225689 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IMDH1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 inosine-5'-monophosphate dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008158 GCST90225690 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PSMA level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 26 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90225691 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PolyUbiquitin K63 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 polyUbiquitin K63-linked measurement http://www.ebi.ac.uk/efo/EFO_0022008 GCST90225692 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MMP-8 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 neutrophil collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008248 GCST90225693 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CATF level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 cathepsin F measurement http://www.ebi.ac.uk/efo/EFO_0022038 GCST90225694 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-22 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90225695 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. vWF level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90225696 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin A level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90225697 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CD39 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90225698 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NET4 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 netrin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020592 GCST90225699 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CLC7A level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 C-type lectin domain family 7 memberAmeasurement http://www.ebi.ac.uk/efo/EFO_0020203 GCST90225700 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. OLR1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 oxidized low-density lipoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020620 GCST90225701 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PHI level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 glucose-6-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020407 GCST90225702 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PLXC1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 plexin-C1 measurement http://www.ebi.ac.uk/efo/EFO_0008266 GCST90225703 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Lysozyme level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90225704 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GRN level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90225705 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CLM6 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90225706 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Coagulation Factor VII level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 prothrombin fragments F1+2 measurement http://www.ebi.ac.uk/efo/EFO_0007776 GCST90225707 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Periostin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90225708 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Esterase D level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 S-formylglutathione hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0008275 GCST90225709 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Apo E2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 apolipoprotein E isoform E2 measurement http://www.ebi.ac.uk/efo/EFO_0008028 GCST90225760 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CKAP2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 cytoskeleton-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020309 GCST90225761 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. RUXF level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 small nuclear ribonucleoprotein F measurement http://www.ebi.ac.uk/efo/EFO_0008288 GCST90225762 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. 14-3-3 protein zeta/delta level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 14-3-3 protein zeta/delta measurement http://www.ebi.ac.uk/efo/EFO_0021996 GCST90225763 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PSME1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90225764 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. UB2G2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 ubiquitin-conjugating enzyme E2 G2 measurement http://www.ebi.ac.uk/efo/EFO_0022035 GCST90225765 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. QORL1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 quinone oxidoreductase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021880 GCST90225766 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Protein C level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90225767 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. VEGF sR3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90225768 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. B7-H2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90225769 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TAJ level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90225770 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FAM3B level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90225771 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IFN-a/b R1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 interferon alpha/beta receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021850 GCST90225772 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Apo L1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90225773 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-17 sR level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90225774 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Arylsulfatase A level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90225775 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Protein disulfide isomerase A3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein disulfide-isomerase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020668 GCST90225776 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PDGFRA level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 4 platelet-derived growth factor receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0021844 GCST90225777 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. YKL-40 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90225778 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NPS-PLA2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90225779 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FGF-19 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90225780 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Hemopexin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 6 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90225781 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Angiopoietin-1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 angiopoietin-1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0010600 GCST90225782 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. WIF-1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 wnt inhibitory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020853 GCST90225783 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. amyloid precursor protein level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 amyloid beta A4 protein measurement http://www.ebi.ac.uk/efo/EFO_0020145 GCST90225784 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. LEG9 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 galectin-9 measurement http://www.ebi.ac.uk/efo/EFO_0021863 GCST90225735 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HEMK2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 hemK methyltransferase family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0021891 GCST90225736 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SMOC1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 sPARC-related modular calcium-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021868 GCST90225737 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MIA level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90225738 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. EMAP-2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 endothelial monocyte-activating polypeptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020348 GCST90225739 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Siglec-7 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90225740 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Kallikrein 11 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90225741 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. kallikrein 8 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90225742 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Luteinizing hormone level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90225743 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. AREG level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 amphiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020144 GCST90225744 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PTP-1B level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90225745 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Siglec-9 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 sialic acid-binding Ig-like lectin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008286 GCST90225746 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DC-SIGN level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90225747 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GPVI level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 platelet glycoprotein VI measurement http://www.ebi.ac.uk/efo/EFO_0008263 GCST90225748 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TrATPase level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90225749 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FSTL3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 follistatin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020394 GCST90225750 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. 14-3-3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 14-3-3 protein family measurement http://www.ebi.ac.uk/efo/EFO_0020109 GCST90225751 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sICAM-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST90225752 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MIC-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90225753 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. EMR2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 adhesion G protein-coupled receptor E2 measurement http://www.ebi.ac.uk/efo/EFO_0021892 GCST90225754 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FUT5 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 alpha-(1,3)-fucosyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020136 GCST90225755 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HCG level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90225756 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. phosphoglycerate kinase 1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 phosphoglycerate kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020638 GCST90225757 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ILT-2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90225758 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SIG14 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90225759 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin S level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 7 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90225785 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GPC2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 glypican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020414 GCST90225786 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TFPI level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90225787 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CAMK1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90225788 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Chitotriosidase-1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90225789 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IgE level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 immunoglobulin E measurement http://www.ebi.ac.uk/efo/EFO_0020464 GCST90225790 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-6 sRa level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90225791 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. AK1A1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 4 alcohol dehydrogenase [NADP(+)] measurement http://www.ebi.ac.uk/efo/EFO_0021977 GCST90225792 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FCRL3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 Fc receptor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008127 GCST90225793 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DERM level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90225794 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GRN level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90225795 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 sRII level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90225796 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C1QR1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90225797 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Hat1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 histone acetyltransferase type b catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0020452 GCST90225798 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PPAC level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90225799 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 R4 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 interleukin 1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008168 GCST90225800 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. KYNU level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 kynureninase measurement http://www.ebi.ac.uk/efo/EFO_0008201 GCST90225801 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Nogo Receptor level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90225802 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Coagulation Factor XI level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 factor XI measurement http://www.ebi.ac.uk/efo/EFO_0004694 GCST90225803 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. VEGF sR3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90225804 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 R AcP level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 1 Receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008167 GCST90225805 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-17 RD level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 17 receptor D measurement http://www.ebi.ac.uk/efo/EFO_0008177 GCST90225806 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BASI level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 basigin measurement http://www.ebi.ac.uk/efo/EFO_0020176 GCST90225807 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Endothelin-converting enzyme 1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90225808 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TXD12 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 15 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90225809 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GPC5 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 glypican-5 measurement http://www.ebi.ac.uk/efo/EFO_0008139 GCST90225710 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Peroxiredoxin-6 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 peroxiredoxin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020631 GCST90225711 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GPC6 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 glypican-6 measurement http://www.ebi.ac.uk/efo/EFO_0021871 GCST90225712 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Galectin-3 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90225713 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Heparin cofactor II level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 heparin cofactor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008150 GCST90225714 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NID2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90225715 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Plasminogen level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 plasma plasminogen measurement http://www.ebi.ac.uk/efo/EFO_0006309 GCST90225716 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-16 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 16 measurement http://www.ebi.ac.uk/efo/EFO_0008173 GCST90225717 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin H level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90225718 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IFN-g level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90225719 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ART level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90225720 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Haptoglobin, Mixed Type level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 7 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90225721 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Nectin-like protein 2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 epithelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010574 GCST90225722 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TPSB2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 2 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90225723 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MMP-2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 72 kda type IV collagenase measurement http://www.ebi.ac.uk/efo/EFO_0020122 GCST90225724 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-34 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 6 interleukin-34 measurement http://www.ebi.ac.uk/efo/EFO_0020505 GCST90225725 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BMP-6 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90225726 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Vitronectin level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 5 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90225727 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MPIF-1 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90225728 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Carbonic Anhydrase IV level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 3 carbonic anhydrase 4 measurement http://www.ebi.ac.uk/efo/EFO_0020230 GCST90225729 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. WFKN2 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90225730 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MIP-5 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90225731 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HCC-4 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90225732 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SREC-I level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 1 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90225733 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Keratin 18 level (CSF) 835 European ancestry individuals NA Illumina [14059245] (imputed) 4 keratin, type I cytoskeletal 18 measurement http://www.ebi.ac.uk/efo/EFO_0020517 GCST90225734 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IGF-II receptor level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90225835 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CK-MB level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 creatine kinase m-type:creatine kinase b-type heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020292 GCST90225836 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. B7-H1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90225837 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. calreticulin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 calreticulin measurement http://www.ebi.ac.uk/efo/EFO_0020221 GCST90225838 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. INGR2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90225839 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. UBP25 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 7 ubiquitin carboxyl-terminal hydrolase 25 measurement http://www.ebi.ac.uk/efo/EFO_0021881 GCST90225840 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. protein Z inhibitor level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90225841 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Coactosin-like protein level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 coactosin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020262 GCST90225842 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. EphB6 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90225843 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Semaphorin 3E level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90225844 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Lectin, mannose-binding 2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 vesicular integral-membrane protein VIP36 measurement http://www.ebi.ac.uk/efo/EFO_0022012 GCST90225845 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FAM3D level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90225846 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FLRT2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 leucine-rich repeat transmembrane protein FLRT2 measurement http://www.ebi.ac.uk/efo/EFO_0021860 GCST90225847 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ISLR2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 immunoglobulin superfamily containing leucine-rich repeat protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021879 GCST90225848 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CD97 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 CD97 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020250 GCST90225849 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DC-SIGN level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90225850 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ATS13 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90225851 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FCN2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 ficolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008135 GCST90225852 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sE-Selectin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90225853 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TLR4:MD-2 complex level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90225854 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. VEGF sR2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90225855 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. complement factor H-related 5 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90225856 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Tenascin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90225857 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ASAH2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90225858 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. LY86 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 lymphocyte antigen 86 measurement http://www.ebi.ac.uk/efo/EFO_0020541 GCST90225859 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HRG level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 histidine-rich glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008155 GCST90225810 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MP2K4 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 dual specificity mitogen-activated protein kinase kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0008113 GCST90225811 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CD27 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 CD27 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008078 GCST90225812 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cripto level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 6 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90225813 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CREL1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 cysteine-rich with EGF-like domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021870 GCST90225814 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HMGN1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 non-histone chromosomal protein HMG-14 measurement http://www.ebi.ac.uk/efo/EFO_0021872 GCST90225815 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Gro-a level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST90225816 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IDUA level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90225817 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ASAHL level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90225818 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. RAP level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90225819 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MIC-1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90225820 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SPARCL1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90225821 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BST1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90225822 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MK11 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 mitogen-activated protein kinase 11 measurement http://www.ebi.ac.uk/efo/EFO_0020575 GCST90225823 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-23 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90225824 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SEM5A level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 semaphorin-5A measurement http://www.ebi.ac.uk/efo/EFO_0021864 GCST90225825 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C7 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90225826 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BGH3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 transforming growth factor-beta-induced protein ig-h3 measurement http://www.ebi.ac.uk/efo/EFO_0008302 GCST90225827 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PDGF Rb level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90225828 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ARTS1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90225829 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TIMD3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90225830 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HGH level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 somatotropin measurement http://www.ebi.ac.uk/efo/EFO_0022017 GCST90225831 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Calpain I level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 calpain I measurement http://www.ebi.ac.uk/efo/EFO_0008064 GCST90225832 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MICA level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 9 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST90225833 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TSP2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90225834 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Angiogenin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90225885 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Caspase-2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 caspase-8 measurement http://www.ebi.ac.uk/efo/EFO_0010764 GCST90225886 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. S100A12 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90225887 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Apo B level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90225888 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C3b level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 complement C3B measurement http://www.ebi.ac.uk/efo/EFO_0020275 GCST90225889 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Apo L1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90225890 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Haptoglobin, Mixed Type level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 12 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90225891 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TPSB2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90225892 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. H31 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 histone H3.1 measurement http://www.ebi.ac.uk/efo/EFO_0021954 GCST90225893 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Semaphorin 3A level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90225894 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. WFKN2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90225895 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SREC-I level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90225896 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TGF-b R III level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 transforming growth factor beta receptor type 3 measurement http://www.ebi.ac.uk/efo/EFO_0020779 GCST90225897 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HEMK2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 hemK methyltransferase family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0021891 GCST90225898 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MIA level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90225899 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TECK level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90225900 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Siglec-6 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 sialic acid-binding Ig-like lectin 6 measurement http://www.ebi.ac.uk/efo/EFO_0008285 GCST90225901 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SPINT2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 Kunitz-type protease inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008200 GCST90225902 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Luteinizing hormone level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90225903 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Siglec-3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90225904 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GPVI level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 platelet glycoprotein VI measurement http://www.ebi.ac.uk/efo/EFO_0008263 GCST90225905 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sICAM-1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST90225906 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Fucosyltransferase 3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 galactoside 34-L-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0008136 GCST90225907 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. G-CSF level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90225908 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HCG level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90225909 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MYPC1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 myosin-binding protein C; slow-type measurement http://www.ebi.ac.uk/efo/EFO_0022013 GCST90225860 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. b-Endorphin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90225861 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. P-Cadherin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 cadherin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020213 GCST90225862 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Contactin-5 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 contactin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008101 GCST90225863 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PDGF-CC level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 platelet-derived growth factor c measurement http://www.ebi.ac.uk/efo/EFO_0020648 GCST90225864 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-17E level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 25 measurement http://www.ebi.ac.uk/efo/EFO_0008182 GCST90225865 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PCSK7 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90225866 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C1-Esterase Inhibitor level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90225867 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MMP-12 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 macrophage metalloelastase measurement http://www.ebi.ac.uk/efo/EFO_0008220 GCST90225868 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. RXFP1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 relaxin receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021950 GCST90225869 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin A level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90225870 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PIK3CA/PIK3R1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 PIK3CA/PIK3R1 measurement http://www.ebi.ac.uk/efo/EFO_0021971 GCST90225871 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. RSPO2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 r-spondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020696 GCST90225872 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Lysozyme level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90225873 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CLM6 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90225874 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Prolactin Receptor level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 prolactin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020656 GCST90225875 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SUMO3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 small ubiquitin-related modifier 3 measurement http://www.ebi.ac.uk/efo/EFO_0022025 GCST90225876 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Coagulation Factor VII level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 prothrombin fragments F1+2 measurement http://www.ebi.ac.uk/efo/EFO_0007776 GCST90225877 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Vasoactive Intestinal Peptide level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 vasoactive intestinal peptide measurement http://www.ebi.ac.uk/efo/EFO_0020849 GCST90225878 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MP2K2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 dual specificity mitogen-activated protein kinase kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008112 GCST90225879 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MAPKAPK3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90225880 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ERP29 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 endoplasmic reticulum resident protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0020346 GCST90225881 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Galectin-3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 2 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90225882 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. HPLN1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 hyaluronan and proteoglycan link protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020459 GCST90225883 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ENTP5 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 4 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90225884 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Moesin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 moesin measurement http://www.ebi.ac.uk/efo/EFO_0020583 GCST90225910 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ILT-2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90225911 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SIG14 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90225912 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BAFF Receptor level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor receptor superfamily member 13C measurement http://www.ebi.ac.uk/efo/EFO_0020804 GCST90225913 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PSME1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90225914 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. QORL1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 quinone oxidoreductase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021880 GCST90225915 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FLRT3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90225916 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Protein C level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 6 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90225917 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CYTF level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90225918 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CYTD level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90225919 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CYTT level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 cystatin-SA measurement http://www.ebi.ac.uk/efo/EFO_0008105 GCST90225920 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Elafin level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90225921 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CPNE1 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 3 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90225922 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ADAMTS-5 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90225923 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. 14-3-3 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 14-3-3 protein family measurement http://www.ebi.ac.uk/efo/EFO_0020109 GCST90225924 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. AFP level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST90225925 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FAM3B level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90225926 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-17 sR level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90225927 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PLXB2 level (plasma) 529 European ancestry individuals NA Illumina [14059245] (imputed) 1 plexin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0021867 GCST90225928 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-10 Ra level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 soluble interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0007650 GCST90225929 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. c-Jun level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 transcription factor AP-1 measurement http://www.ebi.ac.uk/efo/EFO_0021909 GCST90225930 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. YKL-40 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90225931 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin G level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 cathepsin G measurement http://www.ebi.ac.uk/efo/EFO_0020242 GCST90225932 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TACI level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor receptor superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020803 GCST90225933 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Hemopexin level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90225934 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ER level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 estrogen receptor measurement http://www.ebi.ac.uk/efo/EFO_0008125 GCST90225935 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CFC1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 cryptic protein measurement http://www.ebi.ac.uk/efo/EFO_0020293 GCST90225936 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CNTN2 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90225937 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FCG2A level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 low affinity immunoglobulin gamma Fc region receptor II-a measurement http://www.ebi.ac.uk/efo/EFO_0021969 GCST90225938 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. KPCI level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein kinase c iota type measurement http://www.ebi.ac.uk/efo/EFO_0020681 GCST90225939 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DPP2 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90225940 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. AK1A1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 3 alcohol dehydrogenase [NADP(+)] measurement http://www.ebi.ac.uk/efo/EFO_0021977 GCST90225941 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TXD12 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90225942 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sL-Selectin level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90225943 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. cGMP-stimulated PDE level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 cGMP-specific 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0008081 GCST90225944 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C3d level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 complement C3D fragment measurement http://www.ebi.ac.uk/efo/EFO_0020277 GCST90225945 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PGM1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 phosphoglucomutase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021859 GCST90225946 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cathepsin B level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90225947 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IDE level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 insulin-degrading enzyme measurement http://www.ebi.ac.uk/efo/EFO_0020472 GCST90225948 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-18 Ra level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90225949 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PPAC level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 2 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90225950 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Histone H2A.z level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 histone H2A.Z measurement http://www.ebi.ac.uk/efo/EFO_0020454 GCST90225951 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IL-1 R4 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 2 interleukin 1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008168 GCST90225952 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Collectin Kidney 1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90225953 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. FAM107B level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein fam107b measurement http://www.ebi.ac.uk/efo/EFO_0020674 GCST90225954 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IGFBP-1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90225955 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. RAC1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 ras-related c3 botulinum toxin substrate 1 measurement http://www.ebi.ac.uk/efo/EFO_0020699 GCST90225956 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MSP level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 9 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90225957 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Angiopoietin-1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 angiopoietin-1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0010600 GCST90225958 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Growth hormone receptor level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 growth hormone receptor measurement http://www.ebi.ac.uk/efo/EFO_0020426 GCST90225959 Genome-wide genotyping array 2022-11-18 34924174 Mitchell BL 2021-11-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34924174 The Australian Genetics of Depression Study: New Risk Loci and Dissecting Heterogeneity Between Subtypes. Depression 13,318 European ancestry cases, 12,684 European ancestry controls, 246,363 cases, 561,190 controls NA Illumina [7617771] (imputed) 126 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90239706 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. TNF sR-II level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 2 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90225960 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IDUA level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90225961 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ASAHL level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 2 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90225962 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. RET level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 proto-oncogene tyrosine-protein kinase receptor Ret measurement http://www.ebi.ac.uk/efo/EFO_0008272 GCST90225963 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ANGL3 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 angiopoietin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020148 GCST90225964 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. DLL4 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 delta-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020317 GCST90225965 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. IGFBP-7 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90225966 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. JAK2 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 tyrosine-protein kinase JAK2 measurement http://www.ebi.ac.uk/efo/EFO_0020825 GCST90225967 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ARTS1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 3 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90225968 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. sICAM-5 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90225969 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. C4b level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 2 complement C4b measurement http://www.ebi.ac.uk/efo/EFO_0008092 GCST90225970 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SMAD2 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 mothers against decapentaplegic homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0021914 GCST90225971 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. GPNMB level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 3 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90225972 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Ferritin level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90225973 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NXPH1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90225974 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. MED-1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90225975 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. LRIG3 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 leucine-rich repeats and immunoglobulin-like domains protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020534 GCST90225976 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Cystatin-S level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 cystatin-S measurement http://www.ebi.ac.uk/efo/EFO_0020300 GCST90225977 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Fas, soluble level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90225978 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. S100A12 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90225979 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. NET1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 netrin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022009 GCST90225980 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. UFC1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 ubiquitin-fold modifier-conjugating enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020843 GCST90225981 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SAA level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90225982 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Glutathione S-transferase Pi level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90225983 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. OAS1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 2'-5'-oligoadenylate synthase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021911 GCST90225984 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ILT-4 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90225985 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. COLEC12 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90225986 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. PSP level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST90225987 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CDK2/cyclin A level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 cyclin-dependent kinase 2:cyclin-A2 complex measurement http://www.ebi.ac.uk/efo/EFO_0020295 GCST90225988 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. ILT-2 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90225989 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. SIG14 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90225990 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Apo E2 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 apolipoprotein E isoform E2 measurement http://www.ebi.ac.uk/efo/EFO_0008028 GCST90225991 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CPNE1 level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90225992 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. BCMA level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90225993 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Semaphorin 3A level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90225994 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CYTF level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90225995 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. CD30 Ligand level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90225996 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. Arylsulfatase A level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90225997 Genome-wide genotyping array 2022-11-11 34239129 Yang C 2021-07-08 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34239129 Genomic atlas of the proteome from brain, CSF and plasma prioritizes proteins implicated in neurological disorders. pTEN level (brain) 380 European ancestry individuals NA Illumina [14059245] (imputed) 1 phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase pten measurement http://www.ebi.ac.uk/efo/EFO_0020635 GCST90225998 Genome-wide genotyping array 2022-11-11 36230616 Nishizawa D 2022-09-27 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36230616 Genome-Wide Association Study Identifies Candidate Loci Associated with Opioid Analgesic Requirements in the Treatment of Cancer Pain. Opioid analgesic dose requirement in cancer pain treatment 428 Japanese ancestry individuals NA Illumina [648817] 57 response to opioid http://www.ebi.ac.uk/efo/EFO_0008541 GCST90226002 Genome-wide genotyping array 2022-11-25 35377938 Karnes JH 2022-03-04 Blood www.ncbi.nlm.nih.gov/pubmed/35377938 ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia. Heparin-induced thrombocytopenia in PF4/heparin antibody positivity 1,422 European ancestry cases, 1,358 European ancestry controls NA Illumina [9065510] (imputed) 1 response to heparin, Thrombocytopenia http://www.ebi.ac.uk/efo/EFO_0006816, http://purl.obolibrary.org/obo/HP_0001873 GCST90239752 Genome-wide genotyping array 2022-11-24 35220419 Patasova K 2022-02-26 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35220419 A genome-wide analysis of 340 318 participants identifies four novel loci associated with the age of first spectacle wear. Glasses or contact lenses use (age of onset) (UKB data field 2217) 340,318 European ancestry individuals NA Affymetrix [93095623] (imputed) 6 age at initiation of corrective lens use http://www.ebi.ac.uk/efo/EFO_0021781 GCST90239738 Genome-wide genotyping array 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Prevotella_buccalis_SGB_3005) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239753 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Prevotella_denticola_SGB_3531) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239754 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Prevotella_jejuni_SGB_2431) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239755 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Prevotella_sp000599605_SGB_134) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239756 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Prevotella_veroralis_SGB_161) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239757 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Prevotella_unclassified_SGB_144) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239758 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Solobacterium_unclassified_SGB_315) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239759 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Streptococcus_unclassified_SGB_2253) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239760 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Streptococcus_unclassified_SGB_3019) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239761 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Oribacterium_unclassified_SGB_1215) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239762 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Oribacterium_unclassified_SGB_3339) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239763 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Oribacterium_unclassified_SGB_489) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239764 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (F0422_unclassified_SGB_392) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239765 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Veillonella_unclassified_SGB_1075) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239766 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Veillonella_unclassified_SGB_3585) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239767 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Fusobacterium_unclassified_SGB_1140) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239768 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Neisseria_flavescens_SGB_3307) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239769 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Neisseria_unclassified_SGB_1962) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239770 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Tongue microbiota abundance (Neisseria_unclassified_SGB_3316) 2,017 Chinese ancestry individuals 1,333 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239771 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Saliva microbiota abundance (Eggerthia) 1,915 Chinese ancestry individuals 1,299 East Asian ancestry individuals NR [10000000] 8 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239772 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Saliva microbiota abundance (Saccharimonas_unclassified_SGB_271) 1,915 Chinese ancestry individuals 1,299 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239773 Genome-wide sequencing 2022-11-28 34873157 Liu X 2021-12-07 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34873157 Metagenome-genome-wide association studies reveal human genetic impact on the oral microbiome. Saliva microbiota abundance (Oribacterium_unclassified_SGB_3339) 1,915 Chinese ancestry individuals 1,299 East Asian ancestry individuals NR [10000000] 1 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90239774 Genome-wide sequencing 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Albumin levels 148,248 British ancestry men NA Affymetrix [NR] (imputed) 80 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90027079 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Albumin levels 158,000 British ancestry women NA Affymetrix [NR] (imputed) 72 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90027080 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Albumin levels 104,632 British ancestry post-menopausal women NA Affymetrix [NR] (imputed) 47 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90027081 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Albumin levels 36,203 British ancestry pre-menopausal women NA Affymetrix [NR] (imputed) 11 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90027082 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Bioavailable testosterone levels 148,248 British ancestry men NA Affymetrix [NR] (imputed) 73 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027083 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Bioavailable testosterone levels 158,000 British ancestry women NA Affymetrix [NR] (imputed) 66 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027084 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Bioavailable testosterone levels 104,632 British ancestry post-menopausal women NA Affymetrix [NR] (imputed) 78 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027085 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Bioavailable testosterone levels 36,203 British ancestry pre-menopausal women NA Affymetrix [NR] (imputed) 12 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027086 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Free testosterone levels 148,248 British ancestry men NA Affymetrix [NR] (imputed) 68 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027087 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Free testosterone levels 158,000 British ancestry women NA Affymetrix [NR] (imputed) 54 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027088 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Free testosterone levels 104,632 British ancestry post-menopausal women NA Affymetrix [NR] (imputed) 52 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027089 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Free testosterone levels 36,203 British ancestry pre-menopausal women NA Affymetrix [NR] (imputed) 8 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027090 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Sex hormone-binding globulin levels 148,248 British ancestry men NA Affymetrix [NR] (imputed) 171 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90027091 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Sex hormone-binding globulin levels 158,000 British ancestry women NA Affymetrix [NR] (imputed) 135 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90027092 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CA 15 3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 cancer antigen 15.3 measurement http://www.ebi.ac.uk/efo/EFO_0010585 GCST90085712 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Cathepsin D plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 cathepsin D measurement http://www.ebi.ac.uk/efo/EFO_0010611 GCST90085713 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CD40 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 CD40 measurement http://www.ebi.ac.uk/efo/EFO_0010586 GCST90085714 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CD5L plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 CD5 antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0020248 GCST90085715 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CEACAM1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0020251 GCST90085716 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CEACAM6 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 basal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008032 GCST90085717 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CFH plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90085718 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CFHR1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 complement factor H-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600054 GCST90085719 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. cFib plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 fibronectin measurement http://www.ebi.ac.uk/efo/EFO_0008133 GCST90085720 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CTSB plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90085721 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Cystatin B plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 cystatin B measurement http://www.ebi.ac.uk/efo/EFO_0010593 GCST90085722 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Sex hormone-binding globulin levels 36,203 British ancestry pre-menopausal women NA Affymetrix [NR] (imputed) 30 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90027094 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Total testosterone levels 148,248 British ancestry men NA Affymetrix [NR] (imputed) 118 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027095 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. ACE plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 angiotensin-converting enzyme measurement http://www.ebi.ac.uk/efo/EFO_0006515 GCST90085705 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. AGP 1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90085706 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Angiogenin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90085707 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. ANGPTL4 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 angiopoietin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020149 GCST90085708 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Apo C_I plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 apolipoprotein C measurement http://www.ebi.ac.uk/efo/EFO_0020950 GCST90085709 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Apo E plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90085710 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Apo H plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 apolipoprotein H measurement http://www.ebi.ac.uk/efo/EFO_0020951 GCST90085711 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Sex hormone-binding globulin levels 104,632 British ancestry post-menopausal women NA Affymetrix [NR] (imputed) 90 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90027093 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Cystatin C plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90085723 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. DBH plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 dopamine beta-hydroxylase measurement http://www.ebi.ac.uk/efo/EFO_0020952 GCST90085724 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. DKK 1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90085725 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. E Cad plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 2 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90085726 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. E Selectin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90085727 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. EGF plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90085728 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. ENA 78 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 CXCL5 measurement http://www.ebi.ac.uk/efo/EFO_0009422 GCST90085729 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Total testosterone levels 158,000 British ancestry women NA Affymetrix [NR] (imputed) 53 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027096 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Total testosterone levels 104,632 British ancestry post-menopausal women NA Affymetrix [NR] (imputed) 30 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027097 Genome-wide genotyping array 2022-10-24 34321204 Harrison S 2021-07-28 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34321204 Testosterone and socioeconomic position: Mendelian randomization in 306,248 men and women in UK Biobank. Total testosterone levels 36,203 British ancestry pre-menopausal women NA Affymetrix [NR] (imputed) 12 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027098 Genome-wide genotyping array 2022-11-01 36267918 Theriault S 2022-09-24 iScience www.ncbi.nlm.nih.gov/pubmed/36267918 Genome-wide analyses identify SCN5A as a susceptibility locus for premature atrial contraction frequency. Premature atrial contraction frequency 4,831 European ancestry individuals NA Affymetrix, Illumina [9643192] (imputed) 88 Premature atrial contractions http://purl.obolibrary.org/obo/HP_0006699 GCST90134637 Genome-wide genotyping array 2022-11-11 36206743 Aksit MA 2022-10-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36206743 Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis. Meconium ileus in cystic fibrosis 915 European ancestry cases, 3,574 European ancestry controls NA NR [9800000] 7 cystic fibrosis associated meconium ileus http://www.ebi.ac.uk/efo/EFO_0004608 GCST90104458 Genome-wide sequencing 2022-11-11 36206743 Aksit MA 2022-10-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36206743 Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis. Meconium Ileus in Cystic Fibrosis (adjusted for Cystic Fibrosis-Related Diabetes) 817 European ancestry cases, 3,211 European ancestry controls NA NR [9800000] 7 cystic fibrosis associated meconium ileus http://www.ebi.ac.uk/efo/EFO_0004608 GCST90104459 Genome-wide sequencing 2022-11-11 36206743 Aksit MA 2022-10-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36206743 Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis. Cystic fibrosis-related diabetes in cystic fibrosis 1,426 European ancestry cases, 2,682 European ancestry controls NA NR [9800000] 7 cystic fibrosis-related diabetes http://www.ebi.ac.uk/efo/EFO_0801077 GCST90104460 Genome-wide sequencing 2022-11-11 36206743 Aksit MA 2022-10-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36206743 Pleiotropic modifiers of age-related diabetes and neonatal intestinal obstruction in cystic fibrosis. Cystic Fibrosis-Related Diabetes in Cystic Fibrosis (adjusted for Meconium Ileus) 1,396 European ancestry cases, 2,632 European ancestry controls NA NR [9800000] 7 cystic fibrosis-related diabetes http://www.ebi.ac.uk/efo/EFO_0801077 GCST90104461 Genome-wide sequencing 2022-11-04 34721521 Swart Y 2021-10-15 Front Genet www.ncbi.nlm.nih.gov/pubmed/34721521 Local Ancestry Adjusted Allelic Association Analysis Robustly Captures Tuberculosis Susceptibility Loci. Pulmonary tuberculosis 392 South African ancestry cases, 346 South African ancestry controls NA Illumina [4249442] (imputed) 7 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90101733 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MMP 1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90085755 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MMP 10 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 matrix metalloproteinase 10 measurement http://www.ebi.ac.uk/efo/EFO_0010589 GCST90085756 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MMP 3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 matrix metalloproteinase measurement http://www.ebi.ac.uk/efo/EFO_0004744 GCST90085757 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MMP 7 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 matrix metalloproteinase 7 measurement http://www.ebi.ac.uk/efo/EFO_0010591 GCST90085758 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MPIF 1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 CCL23 measurement http://www.ebi.ac.uk/efo/EFO_0009417 GCST90085759 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MSLN plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 mesothelin measurement http://www.ebi.ac.uk/efo/EFO_0020565 GCST90085760 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MSP plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90085761 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. NT proBNP plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 NT-proBNP measurement http://www.ebi.ac.uk/efo/EFO_0004745 GCST90085762 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Omentin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 omentin measurement http://www.ebi.ac.uk/efo/EFO_0020953 GCST90085763 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. PARC plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 C-C motif chemokine 18 measurement http://www.ebi.ac.uk/efo/EFO_0008046 GCST90085764 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. PECAM 1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90085765 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. PEDF plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 pigement epithleium-derived factor (PEDF) measurement http://www.ebi.ac.uk/efo/EFO_0020954 GCST90085766 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. PON 1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 paraoxonase-1 measurement http://www.ebi.ac.uk/efo/EFO_0801085 GCST90085767 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Progranulin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 progranulin measurement http://www.ebi.ac.uk/efo/EFO_0004625 GCST90085768 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. PSP94 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 beta-microseminoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020955 GCST90085769 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. RANTES plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 CCL5 measurement http://www.ebi.ac.uk/efo/EFO_0005117 GCST90085770 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. SAA plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 serum amyloid A protein measurement http://www.ebi.ac.uk/efo/EFO_0004728 GCST90085771 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. SHBG plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90085772 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. SP D plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 surfactant protein D measurement http://www.ebi.ac.uk/efo/EFO_0005081 GCST90085773 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. ST2 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 ST2 protein measurement http://www.ebi.ac.uk/efo/EFO_0010599 GCST90085774 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TAFI plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 thrombin activatable fibrinolysis inhibitor activation peptide measurement http://www.ebi.ac.uk/efo/EFO_0008582 GCST90085775 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TARC plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 CCL17 measurement http://www.ebi.ac.uk/efo/EFO_0009414 GCST90085776 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TATI plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 pancreatic secretory trypsin inhibitor protein measurement http://www.ebi.ac.uk/efo/EFO_0020956 GCST90085777 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TECK plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 CCL25 measurement http://www.ebi.ac.uk/efo/EFO_0010768 GCST90085778 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Tetranectin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 tetranectin measurement http://www.ebi.ac.uk/efo/EFO_0020957 GCST90085779 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Endostatin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 endostatin measurement http://www.ebi.ac.uk/efo/EFO_0020347 GCST90085730 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Eotaxin 2 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90085731 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. ErbB3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 receptor tyrosine-protein kinase erbb-2 measurement http://www.ebi.ac.uk/efo/EFO_0020700 GCST90085732 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. FAS plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90085733 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Fetuin A plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90085734 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Ficolin 3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 ficolin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020392 GCST90085735 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Galectin 3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90085736 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. GDF 15 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90085737 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Haptoglobin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90085738 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. HCC 4 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90085739 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IGFBP 2 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90085740 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IGFBP 3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 IGFBP-3 measurement http://www.ebi.ac.uk/efo/EFO_0004626 GCST90085741 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IL 18 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST90085742 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IL 1RI plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90085743 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IL 1RII plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90085744 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IL 2 receptor_alpha plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 soluble interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0007650 GCST90085745 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IL 6r plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90085746 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Kallikrein 5 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90085747 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. KLK 7 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 kallikrein-7 measurement http://www.ebi.ac.uk/efo/EFO_0008195 GCST90085748 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Lp a plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90085749 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. LRG1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 plasma leucine rich alpha-2-glycoprotein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600050 GCST90085750 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MCP 2 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 monocyte chemotactic protein-2 measurement http://www.ebi.ac.uk/efo/EFO_0010789 GCST90085751 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MCP 4 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 monocyte chemotactic protein-4 measurement http://www.ebi.ac.uk/efo/EFO_0010790 GCST90085752 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MIF plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST90085753 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MIP 1_beta plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 CCL4 measurement http://www.ebi.ac.uk/efo/EFO_0004751 GCST90085754 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TFR1 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 soluble transferrin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004460 GCST90085780 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. THP plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 urinary uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0005663 GCST90085781 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TIE 2 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 angiopoietin-1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0010600 GCST90085782 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TIMP 3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 metalloproteinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008231 GCST90085783 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TN X plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90085784 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. TRAIL R3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 TNF-related apoptosis-inducing ligand measurement http://www.ebi.ac.uk/efo/EFO_0008300 GCST90085785 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Vaspin plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 vaspin measurement http://www.ebi.ac.uk/efo/EFO_0004915 GCST90085786 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. VDBP plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST90085787 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. VEGF plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST90085788 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. VEGFR 2 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 serum VEGFR2 concentration measurement http://www.ebi.ac.uk/efo/EFO_0006795 GCST90085789 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. VEGFR 3 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90085790 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. YKL 40 plasma levels 400 French ancestry individuals NA Illumina [5201092] (imputed) 1 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90085791 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Angiogenin plasma levels conditional to rs11629118 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90085792 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Apo E plasma levels conditional to rs429358 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 APOE carrier status http://www.ebi.ac.uk/efo/EFO_0007659 GCST90085793 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CA 15 3 plasma levels conditional to rs2070803 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 cancer antigen 15.3 measurement http://www.ebi.ac.uk/efo/EFO_0010585 GCST90085794 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. CFHR1 plasma levels conditional to rs60642321 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 complement factor H-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600054 GCST90085795 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. DBH plasma levels conditional to rs2519143 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 dopamine beta-hydroxylase measurement http://www.ebi.ac.uk/efo/EFO_0020952 GCST90085796 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. E Cad plasma levelsrs492602 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90085797 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Eotaxin 2 plasma levels conditional to rs7799486 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90085798 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Haptoglobin plasma levels conditional to rs3213423 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90085799 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IL 2 receptor_alpha plasma levels conditional to rs12722497 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 soluble interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0007650 GCST90085800 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. IL 6r plasma levels conditional to rs12126142 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90085801 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Kallikrein 5 plasma levels conditional to rs11553092 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90085802 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. Lp a plasma levels conditional to rs4646272 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90085803 Genome-wide genotyping array 2022-11-30 35264221 Caron B 2022-03-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/35264221 Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes. MMP 1 plasma levels conditional to rs471994 400 French ancestry individuals NA Illumina [5201092] (imputed) 0 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90085804 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Type 2 diabetes 3,844 Taiwanese ancestry cases, 59,333 Taiwanese ancestry controls NA NR [5925437] (imputed) 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90161239 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Fasting glucose 75,627 Taiwanese ancestry individuals NA NR [5926877] (imputed) 36 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90161236 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Glycated hemoglobin HbA1c levels 76,171 Taiwanese ancestry individuals NA NR [5926877] (imputed) 32 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90161237 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Body mass index 77,060 Taiwanese ancestry individuals NA NR [5925277] (imputed) 32 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90239604 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Body fat percentage 74,231 Taiwanese ancestry individuals NA NR [5925277] (imputed) 18 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90239605 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Waist circumference 76,538 Taiwanese ancestry individuals NA NR [5925277] (imputed) 15 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90239606 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Hip circumference 76,403 Taiwanese ancestry individuals NA NR [5925277] (imputed) 31 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90239607 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Waist-hip ratio 76,894 Taiwanese ancestry individuals NA NR [5925277] (imputed) 11 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90239608 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Total cholesterol levels 76,578 Taiwanese ancestry individuals NA NR [5925277] (imputed) 70 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90239609 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Triglyceride levels 76,053 Taiwanese ancestry individuals NA NR [5925277] (imputed) 32 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90239610 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. High density lipoprotein cholesterol levels 76,531 Taiwanese ancestry individuals NA NR [5925277] (imputed) 63 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90239611 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Low density lipoprotein cholesterol levels 76,650 Taiwanese ancestry individuals NA NR [5925277] (imputed) 53 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90239612 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Very low density lipoprotein cholesterol levels 75,388 Taiwanese ancestry individuals NA NR [5925277] (imputed) 37 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90239613 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Hypertension 9,653 Taiwanese ancestry cases, 59,333 Taiwanese ancestry controls NA NR [5925277] (imputed) 8 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90239614 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Systolic blood pressure 76,466 Taiwanese ancestry individuals NA NR [5925277] (imputed) 22 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90239615 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Diastolic blood pressure 76,607 Taiwanese ancestry individuals NA NR [5925277] (imputed) 24 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90239616 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Pulse rate 76,586 Taiwanese ancestry individuals NA NR [5925277] (imputed) 26 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90239617 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Pulse pressure 76,209 Taiwanese ancestry individuals NA NR [5925277] (imputed) 15 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90239618 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Mean arterial pressure 76,211 Taiwanese ancestry individuals NA NR [5925277] (imputed) 23 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST90239619 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Red blood cell count 76,086 Taiwanese ancestry individuals NA NR [5925277] (imputed) 48 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90239620 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. White blood cell count 76,317 Taiwanese ancestry individuals NA NR [5925277] (imputed) 38 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90239621 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Hemoglobin levels 76,354 Taiwanese ancestry individuals NA NR [5925277] (imputed) 27 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90239622 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Hematocrit 76,452 Taiwanese ancestry individuals NA NR [5925277] (imputed) 32 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90239623 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Platelet count 76,345 Taiwanese ancestry individuals NA NR [5925277] (imputed) 99 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90239624 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Gout 3,140 Taiwanese ancestry cases, 59,333 Taiwanese ancestry controls NA NR [5925277] (imputed) 5 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90239625 Genome-wide genotyping array 2022-10-28 36065016 Zhou W 2022-09-05 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36065016 Multi-omics analysis identifies rare variation in leptin/PPAR gene sets and hypermethylation of ABCG1 contribute to antipsychotics-induced metabolic syndromes. Antipsychotic-induced metabolic syndrome in schizophrenia 416 Chinese ancestry cases, 523 Chinese ancestry controls NA Illumina [6030285] (imputed) 1 response to antipsychotic drug, metabolic syndrome http://purl.obolibrary.org/obo/GO_0097332, http://www.ebi.ac.uk/efo/EFO_0000195 GCST90179476 Genome-wide genotyping array 2022-11-25 35234888 Portilla-Fernandez E 2022-03-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35234888 Genetic and clinical determinants of abdominal aortic diameter: genome-wide association studies, exome array data and Mendelian randomization study. Abdominal aortic diameter 12,815 European ancestry individuals 727 European ancestry individuals Affymetrix, Illumina [8800000] (imputed) 3 descending aortic diameter http://www.ebi.ac.uk/efo/EFO_0021788 GCST90239751 Genome-wide genotyping array 2022-11-28 35305013 Schubert M 2022-03-19 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/35305013 A GWAS in idiopathic/unexplained infertile men detects a genomic region determining Follicle-stimulating hormone levels. Follicle stimulating hormone levels in idiopathic male infertility 742 European ancestry individuals 1,123 European ancestry individuals Illumina [7242305] (imputed) 1 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90239775 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Kidney stones 5,096 Taiwanese ancestry cases, 59,333 Taiwanese ancestry controls NA NR [5925277] (imputed) 1 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90239626 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Blood urea nitrogen levels 76,637 Taiwanese ancestry individuals NA NR [5925277] (imputed) 38 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST90239627 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Creatinine levels 76,850 Taiwanese ancestry individuals NA NR [5925277] (imputed) 58 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90239628 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Uric acid levels 76,779 Taiwanese ancestry individuals NA NR [5925277] (imputed) 41 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90239629 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Urinary microalbumin levels 76,435 Taiwanese ancestry individuals NA NR [5925277] (imputed) 11 urinary microalbumin measurement http://www.ebi.ac.uk/efo/EFO_0010967 GCST90239630 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Total bilirubin levels 76,535 Taiwanese ancestry individuals NA NR [5925277] (imputed) 19 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90239631 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Albumin levels 76,638 Taiwanese ancestry individuals NA NR [5925277] (imputed) 40 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90239632 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Serum glutamic-oxaloacetic transaminase levels 76,168 Taiwanese ancestry individuals NA NR [5925277] (imputed) 16 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90239633 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Serum glutamic-pyruvic transaminase levels 75,881 Taiwanese ancestry individuals NA NR [5925277] (imputed) 10 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90239634 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. AFP levels 76,905 Taiwanese ancestry individuals NA NR [5925277] (imputed) 77 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST90239635 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Liver enzyme levels (gamma-glutamyl transferase) 76,131 Taiwanese ancestry individuals NA NR [5925277] (imputed) 41 protein-glutamine gamma-glutamyltransferase e measurement http://www.ebi.ac.uk/efo/EFO_0020690 GCST90239636 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Gastroesophageal reflux disease 10,226 Taiwanese ancestry cases, 54,389 Taiwanese ancestry controls NA NR [5925277] (imputed) 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90239637 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Headache 2,123 Taiwanese ancestry cases, 54,389 Taiwanese ancestry controls NA NR [5925277] (imputed) 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90239638 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Vertigo 4,527 Taiwanese ancestry cases, 54,389 Taiwanese ancestry controls NA NR [5925277] (imputed) 2 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90239639 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Peptic ulcers 11,389 Taiwanese ancestry cases, 54,389 Taiwanese ancestry controls NA NR [5925277] (imputed) 1 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90239640 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Irritable bowel syndrome 1,892 Taiwanese ancestry cases, 54,389 Taiwanese ancestry controls NA NR [5925277] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90239641 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Asthma 2,641 Taiwanese ancestry cases, 67,097 Taiwanese ancestry controls NA NR [5925277] (imputed) 5 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90239642 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Lung function (FVC) 52,319 Taiwanese ancestry individuals NA NR [5925277] (imputed) 13 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90239643 Genome-wide genotyping array 2022-11-17 36329257 Lee CJ 2022-11-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36329257 Phenome-wide analysis of Taiwan Biobank reveals novel glycemia-related loci and genetic risks for diabetes. Bone stiffness index 75,665 Taiwanese ancestry individuals NA NR [5925277] (imputed) 80 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90239644 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv093) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 2 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133214 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv122) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133215 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: moraxellaceae) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133216 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: neisseriaceae) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133217 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: lactobacillales) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133218 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: haemophilus) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133219 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: rhodobacteraceae) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133220 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv001) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133221 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: actinomycetales) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133222 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: staphylococcus) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133223 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: corynebacterium) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133224 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: clostridiales) at the incertae (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133225 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv009) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133226 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: micrococcaceae) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133227 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: streptococcaceae) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133228 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: bacteroides) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133229 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: anaerococcus) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133230 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: enhydrobacter) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133231 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: micrococcus) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133232 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (phylum: firmicutes) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133233 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: streptococcus) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133234 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv031) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133235 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: chryseobacterium) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133236 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: acinetobacter) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133237 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: paracoccus) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133238 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: chryseobacterium) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133164 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: acinetobacter) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133165 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: paracoccus) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133166 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: rothia) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133167 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv005) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133168 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv013) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133169 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv019) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133170 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv037) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133171 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv002) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133172 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv003) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133173 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: alphaproteobacteria) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133174 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv004) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133175 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv006) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133176 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv008) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133177 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv010) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133178 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv011) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133179 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv012) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133180 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv015) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133181 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv016) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133182 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv021) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133183 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv022) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133184 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: bacteroidales) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133185 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv026) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133186 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv039) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133187 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv042) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133188 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv045) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133189 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv054) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133190 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv057) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133191 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: actinomycetales) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133192 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (phylum: firmicutes) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133193 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (phylum: proteobacteria) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133194 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: bacilli) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133195 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: bacillales) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133196 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: betaproteobacteria) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133197 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: gammaproteobacteria) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133198 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: staphylococcus) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133199 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: neisseriaceae) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133200 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: propionibacterium) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133201 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: corynebacterium) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133202 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv001) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133203 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv005) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133204 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv033) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133205 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv002) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133206 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: burkholderiales) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133207 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv004) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133208 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv007) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133209 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv008) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133210 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv010) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133211 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv013) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133212 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv015) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133213 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: finegoldia) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133239 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: rothia) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133240 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: kocuria) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133241 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv005) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133242 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv007) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133243 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (phylum: proteobacteria) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133244 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv013) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133245 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv019) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133246 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv037) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133247 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv072) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133248 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv002) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133249 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv003) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133250 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv004) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133251 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv006) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133252 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv008) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133253 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv010) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133254 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (phylum: bacteroidetes) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133255 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv011) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133256 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv015) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133257 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv016) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133258 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv021) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133259 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv022) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133260 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv023) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133261 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv035) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133262 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv039) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133263 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: flavobacteriaceae) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133289 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: alphaproteobacteria) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133290 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: bacteroides) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133291 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv070) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133292 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: staphylococcus) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133293 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: burkholderiales) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133294 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: pseudomonadales) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133295 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: neisseriaceae) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133296 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: lactobacillales) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133297 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: rhodobacteraceae) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133298 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: gammaproteobacteria) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133299 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv001) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133300 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: corynebacterium) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133301 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: clostridiales) at the incertae (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133302 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv009) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133303 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: moraxellaceae) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133304 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: micrococcaceae) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133305 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: streptococcaceae) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133306 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: enhydrobacter) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133307 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: micrococcus) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133308 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (genus: streptococcus) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133309 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (family: flavobacteriaceae) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133310 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Multivariate microbial feature (beta-diversity) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133311 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Multivariate microbial feature (beta-diversity) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133312 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Multivariate microbial feature (beta-diversity) at the forehead (sebaceous skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133313 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv042) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133264 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv045) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133265 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: bacilli) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133266 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv053) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133267 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv054) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133268 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv057) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133269 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv059) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133270 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv061) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133271 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv063) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133272 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv065) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133273 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv070) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133274 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv076) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133275 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv086) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133276 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: clostridiales) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133277 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv092) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133278 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv100) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133279 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (asv: asv114) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133280 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: actinomycetales) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133281 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: bacilli) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133282 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (phylum: proteobacteria) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133283 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (phylum: bacteroidetes) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133284 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (order: clostridiales) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133285 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: betaproteobacteria) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133286 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: gammaproteobacteria) at the antecubital fossa (moist skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 1 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133287 Genome-wide genotyping array 2022-12-19 36261456 Moitinho-Silva L 2022-10-19 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36261456 Host genetic factors related to innate immunity, environmental sensing and cellular functions are associated with human skin microbiota. Univariate microbial feature (class: betaproteobacteria) at the dorsal forearm (dry skin) 597 German ancestry individuals NA Affymetrix [4685714] (imputed) 0 skin microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801228 GCST90133288 Genome-wide genotyping array 2022-11-22 35022708 Choquet H 2022-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35022708 Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. Inguinal hernia 461 African American or African ancestry cases, 10,141 African American or African ancestry controls, 33,379 European ancestry cases, 436,717 European ancestry controls, 433 East Asian ancestry cases, 8,318 East Asian ancestry controls, 725 Hispanic or Latin American cases, 6,883 Hispanic or Latin American controls, 435 South Asian ancestry cases, 8,482 South Asian ancestry controls, 341 mixed ancestry cases, 6,805 mixed ancestry controls 559 African American or African ancestry cases, 23,053 African American or African ancestry controls, 30,322 European ancestry cases, 580,593 European ancestry controls, 174 East Asian ancestry cases, 12,619 East Asian ancestry controls, 2,341 Hispanic or Latin American cases, 75,507 Hispanic or Latin American controls, 95 South Asian ancestry cases, 3,155 South Asian ancestry controls Affymetrix [NR] (imputed) 35 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90239723 Genome-wide genotyping array 2022-11-22 35022708 Choquet H 2022-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35022708 Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. Inguinal hernia 461 African American or African ancestry cases, 10,141 African American or African ancestry controls NA Affymetrix [NR] (imputed) 2 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90239724 Genome-wide genotyping array 2022-11-22 35022708 Choquet H 2022-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35022708 Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. Inguinal hernia 33,379 European ancestry cases, 436,717 European ancestry controls NA Affymetrix [NR] (imputed) 16 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90239725 Genome-wide genotyping array 2022-11-22 35022708 Choquet H 2022-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35022708 Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. Inguinal hernia 433 East Asian ancestry cases, 8,318 East Asian ancestry controls NA Affymetrix [NR] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90239726 Genome-wide genotyping array 2022-11-22 35022708 Choquet H 2022-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35022708 Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. Inguinal hernia 32,089 European, African, Asian, Hispanic/Latin American or mixed ancestry male cases, 196,784 European, African, Asian, Hispanic/Latin American or mixed ancestry male controls NA Affymetrix [NR] (imputed) 57 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90239727 Genome-wide genotyping array 2022-11-22 35022708 Choquet H 2022-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35022708 Ancestry- and sex-specific effects underlying inguinal hernia susceptibility identified in a multiethnic genome-wide association study meta-analysis. Inguinal hernia 3,685 European, African, Asian, Hispanic/Latin American or mixed ancestry female cases, 280,562 European, African, Asian, Hispanic/Latin American or mixed ancestry female controls NA Affymetrix [NR] (imputed) 12 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90239728 Genome-wide genotyping array 2022-11-18 36327219 Butler-Laporte G 2022-11-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36327219 Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. Severe COVID-19 disease 5,085 European, African, Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, Native American, South East Asian, East Asian and South Asian ancestry cases, 571,727 European, African, Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, Native American, South East Asian, East Asian and South Asian ancestry controls NA NR [1430342] 8 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90132193 Genome-wide sequencing, Exome-wide sequencing 2022-11-18 36327219 Butler-Laporte G 2022-11-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36327219 Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. COVID-19 (hospitalized vs population) 12,338 European, African, Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, Native American, South East Asian, East Asian and South Asian ancestry cases, 590,465 European, African, Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, Native American, South East Asian, East Asian and South Asian ancestry controls NA NR [1486992] 7 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90132194 Genome-wide sequencing, Exome-wide sequencing 2022-11-18 36327219 Butler-Laporte G 2022-11-03 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36327219 Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. COVID-19 susceptibility 28,266 European, African, Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, Native American, South East Asian, East Asian and South Asian ancestry cases, 597,837 European, African, Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, Native American, South East Asian, East Asian and South Asian ancestry controls NA NR [1530635] 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90132195 Genome-wide sequencing, Exome-wide sequencing 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 252,730 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 176 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179153 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 212,199 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 110 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179154 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 16,816 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179155 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 19,501 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 1 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179156 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 252,730 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 155 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179157 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 212,199 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 91 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179158 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 16,816 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179159 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 19,501 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 1 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179160 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 252,730 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 77 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179161 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 212,199 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 68 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179162 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 16,816 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179163 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 19,501 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 1 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179164 Genome-wide genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 60,343 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179165 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 86,600 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179166 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 60,343 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179167 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 86,600 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179168 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 60,343 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 44 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179169 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 86,600 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179170 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 52,070 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179171 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QT interval 75,607 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90179172 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 52,070 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179173 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. JT interval 75,607 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 JT interval http://www.ebi.ac.uk/efo/EFO_0007885 GCST90179174 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 52,070 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179175 Targeted genotyping array 2022-10-24 36050321 Young WJ 2022-09-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36050321 Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways. QRS duration 75,607 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90179176 Targeted genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Alanine aminotransferase levels 342,387 European ancestry individuals, 6,017 African ancestry individuals, 7,325 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 189 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90019492 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Serum albumin levels 313,032 European ancestry individuals, 5,573 African ancestry individuals, 6,687 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 202 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90019493 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Serum alkaline phosphatase levels 342,535 European ancestry individuals, 6,019 African ancestry individuals, 7,337 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 715 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90019494 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Apolipoprotein A1 levels 311,601 European ancestry individuals, 5,550 African ancestry individuals, 6,682 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 454 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90019495 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Apolipoprotein B levels 340,860 European ancestry individuals, 5,962 African ancestry individuals, 7,275 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 593 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90019496 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Aspartate aminotransferase levels 341,246 European ancestry individuals, 5,982 African ancestry individuals, 7,313 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 265 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90019497 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Aspartate aminotransferase to alanine aminotransferase ratio 341,165 European ancestry individuals, 5,981 African ancestry individuals, 7,309 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 226 aspartate aminotransferase to alanine aminotransferase ratio http://www.ebi.ac.uk/efo/EFO_0010934 GCST90019498 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. C-reactive protein levels 341,805 European ancestry individuals, 6,006 African ancestry individuals, 7,316 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 351 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90019499 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Calcium levels 313,387 European ancestry individuals, 5,576 African ancestry individuals, 6,696 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 208 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90019500 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Total cholesterol levels 342,508 European ancestry individuals, 6,014 African ancestry individuals, 7,336 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 596 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90019501 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Creatinine levels 342,376 European ancestry individuals, 6,016 African ancestry individuals, 7,339 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 359 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90019502 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Urinary creatinine levels 333,115 European ancestry individuals, 5,789 African ancestry individuals, 7,009 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 7 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90019503 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Cystatin C levels 342,399 European ancestry individuals, 6,015 African ancestry individuals, 7,338 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 360 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90019504 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Direct bilirubin levels 291,512 European ancestry individuals, 5,007 African ancestry individuals, 6,088 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 206 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90019505 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Estimated glomerular filtration rate 342,376 European ancestry individuals, 6,016 African ancestry individuals, 7,339 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 349 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90019506 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Gamma glutamyl transferase levels 342,339 European ancestry individuals, 6,015 African ancestry individuals, 7,336 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 424 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90019507 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Blood glucose levels 313,125 European ancestry individuals, 5,568 African ancestry individuals, 6,693 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 121 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90019508 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Glycated hemoglobin levels 327,177 European ancestry individuals, 4,847 African ancestry individuals, 6,895 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 470 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90019509 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. High density lipoprotein cholesterol levels 313,372 European ancestry individuals, 5,573 African ancestry individuals, 6,689 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 519 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90019510 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Insulin-like growth factor 1 levels 340,567 European ancestry individuals, 5,974 African ancestry individuals, 7,283 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 459 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90019511 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Low density lipoprotein cholesterol levels 341,875 European ancestry individuals, 6,003 African ancestry individuals, 7,319 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 563 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90019512 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Lipoprotein (a) levels 272,573 European ancestry individuals, 5,018 African ancestry individuals, 6,453 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 194 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90019513 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Urinary microalbumin levels 102,944 European ancestry individuals, 2,679 African ancestry individuals, 2,560 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 6 urinary microalbumin measurement http://www.ebi.ac.uk/efo/EFO_0010967 GCST90019514 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Non-albumin protein levels 313,032 European ancestry individuals, 5,573 African ancestry individuals, 6,687 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 336 serum non-albumin protein measurement http://www.ebi.ac.uk/efo/EFO_0004568 GCST90019515 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Serum phosphate levels 312,888 European ancestry individuals, 5,568 African ancestry individuals, 6,685 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 188 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90019516 Genome-wide genotyping array 2022-03-28 34993496 Jiang Y 2021-11-19 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34993496 Genetic Factors Associated with Prostate Cancer Conversion from Active Surveillance to Treatment. Conversion from active surveillance to active treatment in prostate cancer 1,609 European ancestry cases, 3,613 European ancestry controls 77 European ancestry cases, 348 European ancestry controls, 123 African ancestry cases, 273 African ancestry controls, 88 Asian ancestry cases, 149 Asian ancestry controls, 21 Latin American cases, 60 Latin American controls Illumina [9962324] (imputed) 14 prostate cancer, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0008315, http://www.ebi.ac.uk/efo/EFO_0008336 GCST90096811 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Allergic rhinitis 13,936 European ancestry cases, 42,701 European ancestry controls NA Affymetrix [15160966] (imputed) 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90086038 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Allergic rhinitis 13,936 European ancestry cases, 42,701 European ancestry controls NA Affymetrix [12148513] (imputed) 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90086039 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Allergic rhinitis 13,936 European ancestry cases, 42,701 European ancestry controls NA Affymetrix [15197755] (imputed) 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90086040 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Allergic rhinitis 13,936 European ancestry cases, 42,701 European ancestry controls NA Affymetrix [11448255] (imputed) 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90086041 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Allergic rhinitis 13,936 European ancestry cases, 42,701 European ancestry controls NA Affymetrix [15644656] (imputed) 4 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90086042 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Asthma 9,209 European ancestry cases, 47,428 European ancestry controls NA Affymetrix [15125630] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90086043 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Asthma 9,209 European ancestry cases, 47,428 European ancestry controls NA Affymetrix [12143954] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90086044 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Asthma 9,209 European ancestry cases, 47,428 European ancestry controls NA Affymetrix [15162203] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90086045 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Asthma 9,209 European ancestry cases, 47,428 European ancestry controls NA Affymetrix [11446434] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90086046 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Asthma 9,209 European ancestry cases, 47,428 European ancestry controls NA Affymetrix [15607971] (imputed) 5 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90086047 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cancer 17,131 European ancestry cases, 39,506 European ancestry controls NA Affymetrix [15130737] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90086048 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cancer 17,131 European ancestry cases, 39,506 European ancestry controls NA Affymetrix [12141565] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90086049 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cancer 17,131 European ancestry cases, 39,506 European ancestry controls NA Affymetrix [15166269] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90086050 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cancer 17,131 European ancestry cases, 39,506 European ancestry controls NA Affymetrix [11445820] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90086051 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cancer 17,131 European ancestry cases, 39,506 European ancestry controls NA Affymetrix [15611556] (imputed) 12 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90086052 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cardiovascular disease 15,009 European ancestry cases, 41,628 European ancestry controls NA Affymetrix [15131276] (imputed) 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90086053 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cardiovascular disease 15,009 European ancestry cases, 41,628 European ancestry controls NA Affymetrix [12132958] (imputed) 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90086054 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cardiovascular disease 15,009 European ancestry cases, 41,628 European ancestry controls NA Affymetrix [15167518] (imputed) 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90086055 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cardiovascular disease 15,009 European ancestry cases, 41,628 European ancestry controls NA Affymetrix [11440238] (imputed) 1 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90086056 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Cardiovascular disease 15,009 European ancestry cases, 41,628 European ancestry controls NA Affymetrix [15613247] (imputed) 2 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90086057 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Major depressive disorder 7,264 European ancestry cases, 49,373 European ancestry controls NA Affymetrix [15107540] (imputed) 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90086058 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Major depressive disorder 7,264 European ancestry cases, 49,373 European ancestry controls NA Affymetrix [12135156] (imputed) 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90086059 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Major depressive disorder 7,264 European ancestry cases, 49,373 European ancestry controls NA Affymetrix [15144048] (imputed) 1 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90086060 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Major depressive disorder 7,264 European ancestry cases, 49,373 European ancestry controls NA Affymetrix [11437905] (imputed) 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90086061 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Major depressive disorder 7,264 European ancestry cases, 49,373 European ancestry controls NA Affymetrix [15589182] (imputed) 1 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90086062 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoporosis 5,399 European ancestry cases, 51,238 European ancestry controls NA Affymetrix [15103307] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90086120 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoporosis 5,399 European ancestry cases, 51,238 European ancestry controls NA Affymetrix [11419007] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90086121 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoporosis 5,399 European ancestry cases, 51,238 European ancestry controls NA Affymetrix [15544346] (imputed) 5 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90086122 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair colour (natural, before greying): Other (UKB data field 1747_6) 5,734 European ancestry cases, 449,430 European ancestry controls NA NR [11842647] (imputed) 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90041841 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Adopted as a child (UKB data field 1767) 6,522 European ancestry cases, 448,808 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90041842 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Part of a multiple birth (UKB data field 1777) 10,333 European ancestry cases, 438,726 European ancestry controls NA NR [11842647] (imputed) 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90041843 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peptic ulcers 920 European ancestry cases, 55,717 European ancestry controls NA Affymetrix [14680546] (imputed) 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90086125 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peptic ulcers 920 European ancestry cases, 55,717 European ancestry controls NA Affymetrix [11304683] (imputed) 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90086126 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peptic ulcers 920 European ancestry cases, 55,717 European ancestry controls NA Affymetrix [15105356] (imputed) 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90086127 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cervical intraepithelial neoplasia [CIN] [Cervical dysplasia] (PheCode 180.3) 1,934 European ancestry cases, 245,606 European ancestry controls NA NR [11842647] (imputed) 0 uterine cervix carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0042487 GCST90041847 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of uterus (PheCode 182) 1,388 European ancestry cases, 246,152 European ancestry controls NA NR [11842647] (imputed) 0 uterine corpus cancer http://www.ebi.ac.uk/efo/EFO_0007532 GCST90041848 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mother still alive (UKB data field 1835) 177,469 European ancestry cases, 271,084 European ancestry controls NA NR [11842647] (imputed) 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90041849 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of ovary (PheCode 184.11) 952 European ancestry cases, 246,588 European ancestry controls NA NR [11842647] (imputed) 0 ovarian neoplasm http://www.ebi.ac.uk/efo/EFO_0003893 GCST90041850 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peripheral vascular disease 4,301 European ancestry cases, 52,336 European ancestry controls NA Affymetrix [15028208] (imputed) 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90086135 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of other female genital organs (PheCode 184) 138 European ancestry cases, 247,402 European ancestry controls NA NR [11842647] (imputed) 0 Genital neoplasm, female http://www.ebi.ac.uk/efo/EFO_1001331 GCST90041852 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of prostate (PheCode 185) 5,796 European ancestry cases, 203,012 European ancestry controls NA NR [11842647] (imputed) 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90041853 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Van drivers (UKB data field 22617_8212) 1,016 European ancestry cases, 112,825 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043553 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Bus and coach drivers (UKB data field 22617_8213) 573 European ancestry cases, 113,268 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043554 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Taxi, cab drivers and chauffeurs (UKB data field 22617_8214) 320 European ancestry cases, 113,521 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043555 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Driving instructors (UKB data field 22617_8215) 160 European ancestry cases, 113,681 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043556 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Rail transport operatives (UKB data field 22617_8216) 212 European ancestry cases, 113,629 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043557 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Seafarers (merchant navy); barge, lighter and boat operatives (UKB data field 22617_8217) 113 European ancestry cases, 113,728 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043558 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Agricultural machinery drivers (UKB data field 22617_8223) 102 European ancestry cases, 113,739 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043559 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Mobile machine drivers and operatives n.e.c. (UKB data field 22617_8229) 131 European ancestry cases, 113,710 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043560 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breathing problems improved/stopped away from workplace or on holiday: No (UKB data field 22618_0) 5,486 European ancestry cases, 108,355 European ancestry controls NA NR [11842647] (imputed) 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90043586 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breathing problems improved/stopped away from workplace or on holiday: Yes (UKB data field 22618_1) 3,361 European ancestry cases, 110,480 European ancestry controls NA NR [11842647] (imputed) 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90043587 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breathing problems responsible for leaving job: No (UKB data field 22619_0) 6,750 European ancestry cases, 107,091 European ancestry controls NA NR [11842647] (imputed) 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90043588 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breathing problems responsible for leaving job: Yes (UKB data field 22619_1) 530 European ancestry cases, 113,311 European ancestry controls NA NR [11842647] (imputed) 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90043589 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job involved shift work: No (UKB data field 22620_0) 107,616 European ancestry cases, 6,225 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043590 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job involved shift work: Yes (UKB data field 22620_1) 32,418 European ancestry cases, 81,423 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043591 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Day shifts worked: Shift pattern was worked for some (but not all) of job (UKB data field 22630_0) 2,194 European ancestry cases, 30,224 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043592 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Day shifts worked: Shift pattern was worked for whole of job (UKB data field 22630_1) 7,769 European ancestry cases, 24,649 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043593 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Day shifts worked: This type of shift pattern was not worked during job (UKB data field 22630_9) 26,022 European ancestry cases, 6,396 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043594 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mixture of day and night shifts worked: Shift pattern was worked for some (but not all) of job (UKB data field 22640_0) 11,515 European ancestry cases, 20,903 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043595 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mixture of day and night shifts worked: Shift pattern was worked for whole of job (UKB data field 22640_1) 16,077 European ancestry cases, 16,341 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043596 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mixture of day and night shifts worked: This type of shift pattern was not worked during job (UKB data field 22640_9) 11,200 European ancestry cases, 21,218 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043597 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Night shifts worked: Shift pattern was worked for some (but not all) of job (UKB data field 22650_0) 1,016 European ancestry cases, 31,402 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043598 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Night shifts worked: Shift pattern was worked for whole of job (UKB data field 22650_1) 1,682 European ancestry cases, 30,736 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043599 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Night shifts worked: This type of shift pattern was not worked during job (UKB data field 22650_9) 31,248 European ancestry cases, 1,170 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043600 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gap coding: Paid work for less than 15 hours per week on average or lasting less than 6 months (UKB data field 22660_101) 18,980 European ancestry cases, 66,707 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043601 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gap coding: Unpaid or voluntary work (UKB data field 22660_102) 3,197 European ancestry cases, 81,436 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043602 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gap coding: Full-time or part-time education (UKB data field 22660_103) 15,778 European ancestry cases, 70,075 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043603 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gap coding: Looking after the home and/or family (UKB data field 22660_105) 30,761 European ancestry cases, 55,639 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043604 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gap coding: Unable to work due to sickness or disability (UKB data field 22660_106) 2,564 European ancestry cases, 81,980 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043605 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gap coding: Unemployed (UKB data field 22660_107) 4,573 European ancestry cases, 80,185 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043606 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gap coding: Retired (UKB data field 22660_108) 66,406 European ancestry cases, 20,899 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043607 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of thyroid glands (PheCode 226) 267 European ancestry cases, 456,081 European ancestry controls NA NR [11842647] (imputed) 0 Benign Thyroid Gland Neoplasm http://www.ebi.ac.uk/efo/EFO_1000122 GCST90043608 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of adrenal gland (PheCode 227.1) 119 European ancestry cases, 456,229 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm of adrenal gland http://purl.obolibrary.org/obo/MONDO_0021511 GCST90043609 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of parathyroid gland (PheCode 227.2) 362 European ancestry cases, 455,986 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm of parathyroid gland http://purl.obolibrary.org/obo/MONDO_0021463 GCST90043610 Genome-wide genotyping array 2022-03-22 34781942 Zhang Z 2021-11-16 BMC Med www.ncbi.nlm.nih.gov/pubmed/34781942 IRF7 and RNH1 are modifying factors of HIV-1 reservoirs: a genome-wide association analysis. CD4+ T cell-associated HIV-1 DNA levels in long-term suppressive antiretroviral treated HIV-1 (adjusted for cell-associated HIV-1 RNA) 207 Dutch ancestry individuals NA Illumina [4307246] (imputed) 1 HIV resevoir measurement http://www.ebi.ac.uk/efo/EFO_0020933 GCST90095667 Genome-wide genotyping array 2022-03-22 34781942 Zhang Z 2021-11-16 BMC Med www.ncbi.nlm.nih.gov/pubmed/34781942 IRF7 and RNH1 are modifying factors of HIV-1 reservoirs: a genome-wide association analysis. CD4+ T cell-associated HIV-1 RNA levels in long-term suppressive antiretroviral treated HIV-1 207 Dutch ancestry individuals NA Illumina [4307246] (imputed) 0 HIV resevoir measurement http://www.ebi.ac.uk/efo/EFO_0020933 GCST90095668 Genome-wide genotyping array 2022-03-22 34781942 Zhang Z 2021-11-16 BMC Med www.ncbi.nlm.nih.gov/pubmed/34781942 IRF7 and RNH1 are modifying factors of HIV-1 reservoirs: a genome-wide association analysis. CD4+ T cell-associated HIV-1 RNA-to-DNA ratio in long-term suppressive antiretroviral treated HIV-1 207 Dutch ancestry individuals NA Illumina [4307246] (imputed) 4 HIV resevoir measurement http://www.ebi.ac.uk/efo/EFO_0020933 GCST90095669 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Agorophobia, social phobia, and panic disorder (PheCode 300.12) 157 European ancestry cases, 456,191 European ancestry controls NA NR [11842647] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90043711 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anxiety disorder (PheCode 300.1) 463 European ancestry cases, 455,885 European ancestry controls NA NR [11842647] (imputed) 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90043712 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture resulting from simple fall (UKB data field 3005) 25,773 European ancestry cases, 17,546 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90043713 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anxiety disorders (PheCode 300) 191 European ancestry cases, 456,157 European ancestry controls NA NR [11842647] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90043714 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Personality disorders (PheCode 301) 102 European ancestry cases, 456,246 European ancestry controls NA NR [11842647] (imputed) 0 Personality disorder http://purl.obolibrary.org/obo/HP_0012075 GCST90043715 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sexual and gender identity disorders (PheCode 302) 198 European ancestry cases, 456,150 European ancestry controls NA NR [11842647] (imputed) 0 gender identity disorder http://www.ebi.ac.uk/efo/EFO_0008587 GCST90043716 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Psychogenic disorder (PheCode 303.3) 310 European ancestry cases, 456,038 European ancestry controls NA NR [11842647] (imputed) 0 Tourette syndrome http://www.ebi.ac.uk/efo/EFO_0004895 GCST90043717 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Adjustment reaction (PheCode 304) 241 European ancestry cases, 456,107 European ancestry controls NA NR [11842647] (imputed) 0 adjustment disorder http://purl.obolibrary.org/obo/MONDO_0003265 GCST90043718 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tension headache (PheCode 306.9) 282 European ancestry cases, 456,066 European ancestry controls NA NR [11842647] (imputed) 0 Tension-type headache http://purl.obolibrary.org/obo/HP_0012228 GCST90043719 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pace maker (UKB data field 3079) 1,433 European ancestry cases, 454,488 European ancestry controls NA NR [11842647] (imputed) 0 artificial cardiac pacemaker http://www.ebi.ac.uk/efo/EFO_0009719 GCST90043720 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured heel (UKB data field 3082) 176 European ancestry cases, 301,811 European ancestry controls NA NR [11842647] (imputed) 0 foot fracture http://www.ebi.ac.uk/efo/EFO_0009618 GCST90043721 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Caffeine drink within last hour (UKB data field 3089) 8,800 European ancestry cases, 409,944 European ancestry controls NA NR [11842647] (imputed) 0 coffee consumption http://www.ebi.ac.uk/efo/EFO_0004330 GCST90043722 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Used an inhaler for chest within last hour (UKB data field 3090) 3,029 European ancestry cases, 415,715 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90043723 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Smoked cigarette or pipe within last hour (UKB data field 3159) 5,483 European ancestry cases, 37,126 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90043724 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substance addiction and disorders (PheCode 316) 1,303 European ancestry cases, 455,045 European ancestry controls NA NR [11842647] (imputed) 0 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST90043725 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcoholic liver damage (PheCode 317.11) 451 European ancestry cases, 455,897 European ancestry controls NA NR [11842647] (imputed) 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90043726 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcoholism (PheCode 317.1) 588 European ancestry cases, 455,760 European ancestry controls NA NR [11842647] (imputed) 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90043727 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcohol-related disorders (PheCode 317) 909 European ancestry cases, 455,439 European ancestry controls NA NR [11842647] (imputed) 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90043728 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Meningitis (PheCode 320) 377 European ancestry cases, 455,971 European ancestry controls NA NR [11842647] (imputed) 0 viral meningitis http://www.ebi.ac.uk/efo/EFO_1001236 GCST90043729 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Encephalitis (PheCode 323) 189 European ancestry cases, 456,159 European ancestry controls NA NR [11842647] (imputed) 0 viral encephalitis http://www.ebi.ac.uk/efo/EFO_0007538 GCST90043730 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sleep apnea (PheCode 327.3) 2,827 European ancestry cases, 453,521 European ancestry controls NA NR [11842647] (imputed) 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90043731 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sleep disorders (PheCode 327) 992 European ancestry cases, 455,356 European ancestry controls NA NR [11842647] (imputed) 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90043732 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hydrocephalus (PheCode 331.1) 154 European ancestry cases, 456,194 European ancestry controls NA NR [11842647] (imputed) 0 Hydrocephalus http://purl.obolibrary.org/obo/HP_0000238 GCST90043733 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Parkinson's disease (PheCode 332) 294 European ancestry cases, 456,054 European ancestry controls NA NR [11842647] (imputed) 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90043734 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Torsion dystonia (PheCode 333.4) 157 European ancestry cases, 456,191 European ancestry controls NA NR [11842647] (imputed) 0 Torsion dystonia http://purl.obolibrary.org/obo/HP_0001304 GCST90043735 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of tobacco previously smoked: Hand-rolled cigarettes (UKB data field 2877_2) 7,577 European ancestry cases, 105,807 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90043686 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of tobacco previously smoked: Cigars or pipes (UKB data field 2877_3) 5,077 European ancestry cases, 108,307 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90043687 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neutropenia (PheCode 288.11) 1,373 European ancestry cases, 454,975 European ancestry controls NA NR [11842647] (imputed) 0 neutropenia http://purl.obolibrary.org/obo/MONDO_0001475 GCST90043688 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of white blood cells (PheCode 288) 135 European ancestry cases, 456,213 European ancestry controls NA NR [11842647] (imputed) 0 functional neutrophil defect http://purl.obolibrary.org/obo/MONDO_0015978 GCST90043689 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Lymphadenitis (PheCode 289.4) 1,425 European ancestry cases, 454,923 European ancestry controls NA NR [11842647] (imputed) 0 Lymphadenitis http://purl.obolibrary.org/obo/HP_0002840 GCST90043690 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Polycythemia, secondary (PheCode 289.8) 192 European ancestry cases, 456,156 European ancestry controls NA NR [11842647] (imputed) 0 secondary polycythemia http://purl.obolibrary.org/obo/MONDO_0020115 GCST90043691 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other diseases of blood and blood-forming organs (PheCode 289) 325 European ancestry cases, 456,023 European ancestry controls NA NR [11842647] (imputed) 0 hematologic disease http://www.ebi.ac.uk/efo/EFO_0005803 GCST90043692 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Delirium due to conditions classified elsewhere (PheCode 290.2) 236 European ancestry cases, 456,112 European ancestry controls NA NR [11842647] (imputed) 0 alcohol withdrawal delirium http://www.ebi.ac.uk/efo/EFO_1000800 GCST90043693 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever stopped smoking for 6 months (UKB data field 2907) 48,297 European ancestry cases, 63,455 European ancestry controls NA NR [11842647] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90043694 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Delirium dementia and amnestic and other cognitive disorders (PheCode 290) 195 European ancestry cases, 456,153 European ancestry controls NA NR [11842647] (imputed) 0 cognitive disorder http://purl.obolibrary.org/obo/MONDO_0002039 GCST90043695 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Transient mental disorders due to conditions classified elsewhere (PheCode 291.1) 112 European ancestry cases, 456,236 European ancestry controls NA NR [11842647] (imputed) 0 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST90043696 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alteration of consciousness (PheCode 291.8) 202 European ancestry cases, 456,146 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of mental function http://purl.obolibrary.org/obo/HP_0011446 GCST90043697 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aphasia/speech disturbance (PheCode 292.1) 407 European ancestry cases, 455,941 European ancestry controls NA NR [11842647] (imputed) 0 Aphasia http://purl.obolibrary.org/obo/HP_0002381 GCST90043698 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Memory loss (PheCode 292.3) 250 European ancestry cases, 456,098 European ancestry controls NA NR [11842647] (imputed) 0 amnesia http://www.ebi.ac.uk/efo/EFO_1001454 GCST90043699 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Altered mental status (PheCode 292.4) 816 European ancestry cases, 455,532 European ancestry controls NA NR [11842647] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90043700 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neurological disorders (PheCode 292) 144 European ancestry cases, 456,204 European ancestry controls NA NR [11842647] (imputed) 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90043701 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Swelling, mass, or lump in head and neck [Space-occupying lesion, intracranial, not otherwise specified] (PheCode 293.1) 707 European ancestry cases, 455,641 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of head or neck http://purl.obolibrary.org/obo/HP_0000152 GCST90043702 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms involving head and neck (PheCode 293) 1,670 European ancestry cases, 454,678 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of head or neck http://purl.obolibrary.org/obo/HP_0000152 GCST90043703 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Schizophrenia (PheCode 295.1) 367 European ancestry cases, 455,981 European ancestry controls NA NR [11842647] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90043704 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Paranoid disorders (PheCode 295.2) 106 European ancestry cases, 456,242 European ancestry controls NA NR [11842647] (imputed) 0 Paranoia http://purl.obolibrary.org/obo/HP_0011999 GCST90043705 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Psychosis (PheCode 295.3) 102 European ancestry cases, 456,246 European ancestry controls NA NR [11842647] (imputed) 0 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST90043706 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. General pain for three months (UKB data field 2956) 5,939 European ancestry cases, 1,198 European ancestry controls NA NR [11842647] (imputed) 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90043707 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bipolar (PheCode 296.1) 628 European ancestry cases, 455,720 European ancestry controls NA NR [11842647] (imputed) 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90043708 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Major depressive disorder (PheCode 296.22) 376 European ancestry cases, 455,972 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90043709 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Started insulin within one year diabetes mellitis diagnosis (UKB data field 2986) 2,551 European ancestry cases, 18,341 European ancestry controls NA NR [11842647] (imputed) 0 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90043710 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dermatophytosis 7,676 European ancestry cases, 48,961 European ancestry controls NA Affymetrix [15122260] (imputed) 0 dermatophytosis http://purl.obolibrary.org/obo/MONDO_0004678 GCST90086063 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dermatophytosis 7,676 European ancestry cases, 48,961 European ancestry controls NA Affymetrix [12144114] (imputed) 0 dermatophytosis http://purl.obolibrary.org/obo/MONDO_0004678 GCST90086064 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dermatophytosis 7,676 European ancestry cases, 48,961 European ancestry controls NA Affymetrix [15158554] (imputed) 0 dermatophytosis http://purl.obolibrary.org/obo/MONDO_0004678 GCST90086065 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dermatophytosis 7,676 European ancestry cases, 48,961 European ancestry controls NA Affymetrix [11444240] (imputed) 0 dermatophytosis http://purl.obolibrary.org/obo/MONDO_0004678 GCST90086066 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dermatophytosis 7,676 European ancestry cases, 48,961 European ancestry controls NA Affymetrix [15603217] (imputed) 0 dermatophytosis http://purl.obolibrary.org/obo/MONDO_0004678 GCST90086067 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Type 2 diabetes 6,967 European ancestry cases, 49,670 European ancestry controls NA Affymetrix [15053455] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90086068 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Type 2 diabetes 6,967 European ancestry cases, 49,670 European ancestry controls NA Affymetrix [12101429] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90086069 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Type 2 diabetes 6,967 European ancestry cases, 49,670 European ancestry controls NA Affymetrix [15089890] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90086070 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Type 2 diabetes 6,967 European ancestry cases, 49,670 European ancestry controls NA Affymetrix [11417486] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90086071 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Type 2 diabetes 6,967 European ancestry cases, 49,670 European ancestry controls NA Affymetrix [15533686] (imputed) 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90086072 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dyslipidemia 30,244 European ancestry cases, 26,393 European ancestry controls NA Affymetrix [15194005] (imputed) 0 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST90086073 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dyslipidemia 30,244 European ancestry cases, 26,393 European ancestry controls NA Affymetrix [12156151] (imputed) 0 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST90086074 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dyslipidemia 30,244 European ancestry cases, 26,393 European ancestry controls NA Affymetrix [15231200] (imputed) 0 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST90086075 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dyslipidemia 30,244 European ancestry cases, 26,393 European ancestry controls NA Affymetrix [11454155] (imputed) 0 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST90086076 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Dyslipidemia 30,244 European ancestry cases, 26,393 European ancestry controls NA Affymetrix [15679186] (imputed) 23 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST90086077 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hemorrhoids 9,129 European ancestry cases, 47,508 European ancestry controls NA Affymetrix [15131970] (imputed) 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90086078 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hemorrhoids 9,129 European ancestry cases, 47,508 European ancestry controls NA Affymetrix [12145383] (imputed) 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90086079 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hemorrhoids 9,129 European ancestry cases, 47,508 European ancestry controls NA Affymetrix [15168441] (imputed) 1 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90086080 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hemorrhoids 9,129 European ancestry cases, 47,508 European ancestry controls NA Affymetrix [11445893] (imputed) 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90086081 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hemorrhoids 9,129 European ancestry cases, 47,508 European ancestry controls NA Affymetrix [15614723] (imputed) 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90086082 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hernia abdominopelvic cavity 6,291 European ancestry cases, 50,346 European ancestry controls NA Affymetrix [15085878] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90086083 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hernia abdominopelvic cavity 6,291 European ancestry cases, 50,346 European ancestry controls NA Affymetrix [12122434] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90086084 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hernia abdominopelvic cavity 6,291 European ancestry cases, 50,346 European ancestry controls NA Affymetrix [15122482] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90086085 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hernia abdominopelvic cavity 6,291 European ancestry cases, 50,346 European ancestry controls NA Affymetrix [11425307] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90086086 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hernia abdominopelvic cavity 6,291 European ancestry cases, 50,346 European ancestry controls NA Affymetrix [15565029] (imputed) 4 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90086087 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Had menopause (UKB data field 2724) 151,787 European ancestry cases, 56,174 European ancestry controls NA NR [11842647] (imputed) 0 menopause http://www.ebi.ac.uk/efo/EFO_0003922 GCST90043661 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gout (PheCode 274.1) 375 European ancestry cases, 455,973 European ancestry controls NA NR [11842647] (imputed) 1 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90043662 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chondrocalcinosis (PheCode 274.21) 236 European ancestry cases, 456,112 European ancestry controls NA NR [11842647] (imputed) 0 Chondrocalcinosis http://purl.obolibrary.org/obo/HP_0000934 GCST90043663 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of iron metabolism (PheCode 275.1) 643 European ancestry cases, 455,705 European ancestry controls NA NR [11842647] (imputed) 1 metabolic disease http://www.ebi.ac.uk/efo/EFO_0000589 GCST90043664 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of calcium/phosphorus metabolism (PheCode 275.5) 353 European ancestry cases, 455,995 European ancestry controls NA NR [11842647] (imputed) 0 metabolic disease http://www.ebi.ac.uk/efo/EFO_0000589 GCST90043665 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hyposmolality and/or hyponatremia (PheCode 276.12) 356 European ancestry cases, 455,992 European ancestry controls NA NR [11842647] (imputed) 0 Hyponatremia, Abnormal blood ion concentration http://purl.obolibrary.org/obo/HP_0002902, http://purl.obolibrary.org/obo/HP_0003111 GCST90043666 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hyperpotassemia (PheCode 276.13) 322 European ancestry cases, 456,026 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of metabolism/homeostasis http://purl.obolibrary.org/obo/HP_0001939 GCST90043667 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypopotassemia (PheCode 276.14) 135 European ancestry cases, 456,213 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of metabolism/homeostasis http://purl.obolibrary.org/obo/HP_0001939 GCST90043668 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypovolemia (PheCode 276.5) 343 European ancestry cases, 456,005 European ancestry controls NA NR [11842647] (imputed) 0 Hypovolemia http://purl.obolibrary.org/obo/HP_0011106 GCST90043669 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had stillbirth, spontaneous miscarriage or termination (UKB data field 2774) 77,569 European ancestry cases, 166,108 European ancestry controls NA NR [11842647] (imputed) 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90043670 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of metabolism (PheCode 277) 112 European ancestry cases, 456,236 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of glycosaminoglycan metabolism http://purl.obolibrary.org/obo/HP_0004371 GCST90043671 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Obesity (PheCode 278.1) 581 European ancestry cases, 455,767 European ancestry controls NA NR [11842647] (imputed) 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90043672 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever taken oral contraceptive pill (UKB data field 2784) 202,628 European ancestry cases, 44,253 European ancestry controls NA NR [11842647] (imputed) 0 contraception http://www.ebi.ac.uk/efo/EFO_0009520 GCST90043673 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other immunological findings (PheCode 279.7) 148 European ancestry cases, 456,200 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the immune system http://purl.obolibrary.org/obo/HP_0002715 GCST90043674 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Iron deficiency anemias, unspecified or not due to blood loss (PheCode 280.1) 4,736 European ancestry cases, 451,612 European ancestry controls NA NR [11842647] (imputed) 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90043675 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Iron deficiency anemia secondary to blood loss (chronic) (PheCode 280.2) 124 European ancestry cases, 456,224 European ancestry controls NA NR [11842647] (imputed) 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90043676 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever used hormone replacement therapy (UKB data field 2814) 96,860 European ancestry cases, 149,888 European ancestry controls NA NR [11842647] (imputed) 0 hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0003961 GCST90043677 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bilateral oophorectomy (UKB data field 2834) 19,868 European ancestry cases, 224,134 European ancestry controls NA NR [11842647] (imputed) 0 bilateral oophorectomy http://www.ebi.ac.uk/efo/EFO_0009717 GCST90043678 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Had other major operations (UKB data field 2844) 164,856 European ancestry cases, 80,452 European ancestry controls NA NR [11842647] (imputed) 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90043679 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aplastic anemia (PheCode 284) 197 European ancestry cases, 456,151 European ancestry controls NA NR [11842647] (imputed) 0 Pure red cell aplasia http://purl.obolibrary.org/obo/HP_0012410 GCST90043680 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anemia in neoplastic disease (PheCode 285.22) 128 European ancestry cases, 456,220 European ancestry controls NA NR [11842647] (imputed) 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90043681 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other anemias (PheCode 285) 5,492 European ancestry cases, 450,856 European ancestry controls NA NR [11842647] (imputed) 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90043682 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Primary thrombocytopenia (PheCode 287.31) 260 European ancestry cases, 456,088 European ancestry controls NA NR [11842647] (imputed) 0 primary thrombocytopenia http://purl.obolibrary.org/obo/MONDO_0004680 GCST90043683 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Thrombocytopenia (PheCode 287.3) 296 European ancestry cases, 456,052 European ancestry controls NA NR [11842647] (imputed) 0 Thrombocytopenia http://purl.obolibrary.org/obo/HP_0001873 GCST90043684 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of tobacco previously smoked: Manufactured cigarettes (UKB data field 2877_1) 100,730 European ancestry cases, 12,654 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90043685 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Acute reaction to stress 4,314 European ancestry cases, 52,323 European ancestry controls NA Affymetrix [15038126] (imputed) 0 acute stress reaction http://www.ebi.ac.uk/efo/EFO_0005223 GCST90086138 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Acute reaction to stress 4,314 European ancestry cases, 52,323 European ancestry controls NA Affymetrix [12089300] (imputed) 0 acute stress reaction http://www.ebi.ac.uk/efo/EFO_0005223 GCST90086139 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Acute reaction to stress 4,314 European ancestry cases, 52,323 European ancestry controls NA Affymetrix [15075110] (imputed) 0 acute stress reaction http://www.ebi.ac.uk/efo/EFO_0005223 GCST90086140 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Acute reaction to stress 4,314 European ancestry cases, 52,323 European ancestry controls NA Affymetrix [11399727] (imputed) 0 acute stress reaction http://www.ebi.ac.uk/efo/EFO_0005223 GCST90086141 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Acute reaction to stress 4,314 European ancestry cases, 52,323 European ancestry controls NA Affymetrix [15517788] (imputed) 1 acute stress reaction http://www.ebi.ac.uk/efo/EFO_0005223 GCST90086142 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Varicose veins 2,483 European ancestry cases, 54,154 European ancestry controls NA Affymetrix [14877783] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90086143 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Varicose veins 2,483 European ancestry cases, 54,154 European ancestry controls NA Affymetrix [12017028] (imputed) 1 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90086144 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Varicose veins 2,483 European ancestry cases, 54,154 European ancestry controls NA Affymetrix [14912954] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90086145 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Varicose veins 2,483 European ancestry cases, 54,154 European ancestry controls NA Affymetrix [11347478] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90086146 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Varicose veins 2,483 European ancestry cases, 54,154 European ancestry controls NA Affymetrix [15348957] (imputed) 2 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90086147 Genome-wide genotyping array 2021-12-01 34586716 Chen J 2021-09-29 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/34586716 Heritability and genome-wide association study of blood pressure in Chinese adult twins. Systolic blood pressure 137 Chinese ancestry twins NA Illumina [7401356] (imputed) 21 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90058960 Genome-wide genotyping array 2021-12-01 34586716 Chen J 2021-09-29 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/34586716 Heritability and genome-wide association study of blood pressure in Chinese adult twins. Diastolic blood pressure 137 Chinese ancestry twins NA Illumina [7401356] (imputed) 16 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90058961 Genome-wide genotyping array 2021-12-01 34586716 Chen J 2021-09-29 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/34586716 Heritability and genome-wide association study of blood pressure in Chinese adult twins. Pulse pressure 137 Chinese ancestry twins NA Illumina [7401356] (imputed) 24 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90058962 Genome-wide genotyping array 2021-12-01 34586716 Chen J 2021-09-29 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/34586716 Heritability and genome-wide association study of blood pressure in Chinese adult twins. Mean arterial pressure 137 Chinese ancestry twins NA Illumina [7401356] (imputed) 20 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST90058963 Genome-wide genotyping array 2022-09-08 35776183 Hertz DL 2022-07-01 Support Care Cancer www.ncbi.nlm.nih.gov/pubmed/35776183 Genome-wide association study of aromatase inhibitor discontinuation due to musculoskeletal symptoms. Aromatase inhibitors induced musculoskeletal syndrome in HR+ non-metastatic breast cancer 400 White ancestry individuals NA NR [NR] (imputed) 51 musculoskeletal system disease, response to aromatase inhibitor http://www.ebi.ac.uk/efo/EFO_0009676, http://purl.obolibrary.org/obo/GO_0061477 GCST90134417 Genome-wide genotyping array 2022-09-08 35776183 Hertz DL 2022-07-01 Support Care Cancer www.ncbi.nlm.nih.gov/pubmed/35776183 Genome-wide association study of aromatase inhibitor discontinuation due to musculoskeletal symptoms. Exemestane induced musculoskeletal syndrome in HR+ non-metastatic breast cancer 201 White ancestry individuals NA NR [NR] (imputed) 39 musculoskeletal system disease, response to aromatase inhibitor http://www.ebi.ac.uk/efo/EFO_0009676, http://purl.obolibrary.org/obo/GO_0061477 GCST90134418 Genome-wide genotyping array 2022-09-08 35776183 Hertz DL 2022-07-01 Support Care Cancer www.ncbi.nlm.nih.gov/pubmed/35776183 Genome-wide association study of aromatase inhibitor discontinuation due to musculoskeletal symptoms. Letrozole induced musculoskeletal syndrome in HR+ non-metastatic breast cancer 319 White ancestry individuals NA NR [NR] (imputed) 26 musculoskeletal system disease, response to aromatase inhibitor http://www.ebi.ac.uk/efo/EFO_0009676, http://purl.obolibrary.org/obo/GO_0061477 GCST90134419 Genome-wide genotyping array 2022-03-16 34834521 Hsiao YJ 2021-11-09 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834521 Genome-Wide Polygenic Risk Score for Predicting High Risk Glaucoma Individuals of Han Chinese Ancestry. Glaucoma 1,013 Han Chinese ancestry cases, 36,562 Han Chinese ancestry controls NA NR [11110260] (imputed) 138 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90095474 Genome-wide genotyping array 2022-01-24 34847907 Tegelberg P 2021-11-30 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/34847907 Genome-wide association study of periodontal pocketing in Finnish adults. Periodontal pocket (adjusted for age and sex) 3,906 Finnish ancestry individuals NA Illumina [NR] (imputed) 8 Periodontal Pocket http://www.ebi.ac.uk/efo/EFO_1001393 GCST90093139 Genome-wide genotyping array 2022-01-24 34847907 Tegelberg P 2021-11-30 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/34847907 Genome-wide association study of periodontal pocketing in Finnish adults. Periodontal pocket (adjusted for age, sex and smoking status) 3,906 Finnish ancestry individuals NA Illumina [NR] (imputed) 5 Periodontal Pocket http://www.ebi.ac.uk/efo/EFO_1001393 GCST90093140 Genome-wide genotyping array 2022-01-24 34847907 Tegelberg P 2021-11-30 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/34847907 Genome-wide association study of periodontal pocketing in Finnish adults. Periodontal pocket (adjusted for age, sex, smoking status and plaque) 3,906 Finnish ancestry individuals NA Illumina [NR] (imputed) 5 Periodontal Pocket http://www.ebi.ac.uk/efo/EFO_1001393 GCST90093141 Genome-wide genotyping array 2022-03-25 34523676 Jager S 2021-09-15 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34523676 Blood copper and risk of cardiometabolic diseases-A Mendelian randomization study. Copper levels 6,937 European or unknown ancestry individuals NA Illumina [NR] (imputed) 2 blood copper measurement http://www.ebi.ac.uk/efo/EFO_0007578 GCST90096810 Genome-wide genotyping array 2022-03-16 34836252 Irvin MR 2021-11-10 Nutrients www.ncbi.nlm.nih.gov/pubmed/34836252 Genomics of Postprandial Lipidomics in the Genetics of Lipid-Lowering Drugs and Diet Network Study. Postprandial lipemia response 668 European ancestry individuals 639 individuals Affymetrix [906600] 0 lipid change measurement http://www.ebi.ac.uk/efo/EFO_0020859 GCST90095479 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Medium chain acylcarnitines levels (dominant genetic model) up to 1,490 European ancestry individuals up to 2,022 European ancestry individuals Illumina [NR] 6 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104877 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Medium chain acylcarnitines levels (additive genetic model) up to 1,490 Black individuals up to 2,022 Black individuals Illumina [NR] 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104878 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Medium chain acylcarnitines levels (dominant genetic model) up to 1,490 Black individuals up to 2,022 Black individuals Illumina [NR] 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104879 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Long-chain dicarboxylacylcarnitines levels (additive genetic model) up to 1,490 European ancestry individuals up to 2,022 European ancestry individuals Illumina [NR] 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104880 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Long-chain dicarboxylacylcarnitines levels (additive genetic model) up to 1,490 Black individuals up to 2,022 Black individuals Illumina [NR] 9 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104881 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Long-chain dicarboxylacylcarnitines levels (dominant genetic model) up to 1,490 Black individuals up to 2,022 Black individuals Illumina [NR] 4 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104882 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Long-chain dicarboxylacylcarnitines levels (dominant genetic model) up to 1,490 European ancestry individuals up to 2,022 European ancestry individuals Illumina [NR] 3 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104883 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Short-chain dicarboxylacylcarnitine levels (additive genetic model) up to 1,490 European ancestry individuals up to 2,022 European ancestry individuals Illumina [NR] 9 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104885 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Short-chain dicarboxylacylcarnitine levels (dominant genetic model) up to 1,490 Black individuals up to 2,022 Black individuals Illumina [NR] 1 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104887 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Medium chain acylcarnitines levels (additive genetic model) 1,490 European ancestry, Black individuals 2,022 European ancestry, Black individuals Illumina [NR] 10 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104888 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Medium chain acylcarnitines levels (dominant genetic model) 1,490 European ancestry, Black individuals 2,022 European ancestry, Black individuals Illumina [NR] 6 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104889 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Long-chain dicarboxylacylcarnitines levels (additive genetic model) 1,490 European ancestry, Black individuals 2,022 European ancestry, Black individuals Illumina [NR] 6 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104890 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Long-chain dicarboxylacylcarnitines levels (dominant genetic model) 1,490 European ancestry, Black individuals 2,022 European ancestry, Black individuals Illumina [NR] 2 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104891 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Short-chain dicarboxylacylcarnitine levels (dominant genetic model) 1,490 European ancestry, Black individuals 2,022 European ancestry, Black individuals Illumina [NR] 11 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104893 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Medium chain acylcarnitines levels (additive genetic model) up to 1,490 European ancestry individuals up to 2,022 European ancestry individuals Illumina [NR] 6 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104876 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Short-chain dicarboxylacylcarnitine levels (additive genetic model) up to 1,490 Black individuals up to 2,022 Black individuals Illumina [NR] 3 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104884 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Short-chain dicarboxylacylcarnitine levels (dominant genetic model) up to 1,490 European ancestry individuals up to 2,022 European ancestry individuals Illumina [NR] 5 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104886 Genome-wide genotyping array 2022-07-01 26540294 Kraus WE 2015-11-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/26540294 Metabolomic Quantitative Trait Loci (mQTL) Mapping Implicates the Ubiquitin Proteasome System in Cardiovascular Disease Pathogenesis. Short-chain dicarboxylacylcarnitine levels (additive genetic model) 1,490 European ancestry, Black individuals 2,022 European ancestry, Black individuals Illumina [NR] 11 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90104892 Genome-wide genotyping array 2022-03-15 34749984 Borgio JF 2021-11-04 Comput Biol Med www.ncbi.nlm.nih.gov/pubmed/34749984 Exome array identifies functional exonic biomarkers for pediatric dental caries. Pediatric dental caries (decayed, missing and filled teeth >5) 76 Arab ancestry cases, 35 Arab ancestry controls NA Illumina [243345] 7 primary dental caries http://www.ebi.ac.uk/efo/EFO_0600095 GCST90095189 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoarthritis 20,212 European ancestry cases, 36,425 European ancestry controls NA Affymetrix [15180137] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90086113 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoarthritis 20,212 European ancestry cases, 36,425 European ancestry controls NA Affymetrix [12151861] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90086114 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoarthritis 20,212 European ancestry cases, 36,425 European ancestry controls NA Affymetrix [15216599] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90086115 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoarthritis 20,212 European ancestry cases, 36,425 European ancestry controls NA Affymetrix [11450581] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90086116 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoarthritis 20,212 European ancestry cases, 36,425 European ancestry controls NA Affymetrix [15663970] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90086117 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoporosis 5,399 European ancestry cases, 51,238 European ancestry controls NA Affymetrix [15066946] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90086118 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Osteoporosis 5,399 European ancestry cases, 51,238 European ancestry controls NA Affymetrix [12116316] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90086119 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair colour (natural, before greying): Red (UKB data field 1747_2) 20,692 European ancestry cases, 434,472 European ancestry controls NA NR [11842647] (imputed) 90 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90041837 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair colour (natural, before greying): Light brown (UKB data field 1747_3) 185,000 European ancestry cases, 270,164 European ancestry controls NA NR [11842647] (imputed) 13 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90041838 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair colour (natural, before greying): Dark brown (UKB data field 1747_4) 171,614 European ancestry cases, 283,550 European ancestry controls NA NR [11842647] (imputed) 64 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90041839 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair colour (natural, before greying): Black (UKB data field 1747_5) 20,700 European ancestry cases, 434,464 European ancestry controls NA NR [11842647] (imputed) 16 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90041840 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peptic ulcers 920 European ancestry cases, 55,717 European ancestry controls NA Affymetrix [14647167] (imputed) 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90086123 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peptic ulcers 920 European ancestry cases, 55,717 European ancestry controls NA Affymetrix [11954126] (imputed) 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90086124 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Maternal smoking around birth (UKB data field 1787) 120,297 European ancestry cases, 271,695 European ancestry controls NA NR [11842647] (imputed) 0 environmental tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0008361 GCST90041844 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Father still alive (UKB data field 1797) 102,290 European ancestry cases, 341,738 European ancestry controls NA NR [11842647] (imputed) 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90041845 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cervical cancer (PheCode 180.1) 258 European ancestry cases, 247,282 European ancestry controls NA NR [11842647] (imputed) 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90041846 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Neuropsychiatric disorders 8,624 European ancestry cases, 48,013 European ancestry controls NA Affymetrix [15138972] (imputed) 0 psychiatric disorder http://purl.obolibrary.org/obo/MONDO_0002025 GCST90086128 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Neuropsychiatric disorders 8,624 European ancestry cases, 48,013 European ancestry controls NA Affymetrix [12148126] (imputed) 0 psychiatric disorder http://purl.obolibrary.org/obo/MONDO_0002025 GCST90086129 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Neuropsychiatric disorders 8,624 European ancestry cases, 48,013 European ancestry controls NA Affymetrix [15175619] (imputed) 1 psychiatric disorder http://purl.obolibrary.org/obo/MONDO_0002025 GCST90086130 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Neuropsychiatric disorders 8,624 European ancestry cases, 48,013 European ancestry controls NA Affymetrix [11446583] (imputed) 0 psychiatric disorder http://purl.obolibrary.org/obo/MONDO_0002025 GCST90086131 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Neuropsychiatric disorders 8,624 European ancestry cases, 48,013 European ancestry controls NA Affymetrix [15621994] (imputed) 1 psychiatric disorder http://purl.obolibrary.org/obo/MONDO_0002025 GCST90086132 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peripheral vascular disease 4,301 European ancestry cases, 52,336 European ancestry controls NA Affymetrix [14992808] (imputed) 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90086133 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peripheral vascular disease 4,301 European ancestry cases, 52,336 European ancestry controls NA Affymetrix [12080827] (imputed) 2 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90086134 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of other female genital organs (excluding uterus and ovary) (PheCode 184.2) 316 European ancestry cases, 247,224 European ancestry controls NA NR [11842647] (imputed) 0 Genital neoplasm, female http://www.ebi.ac.uk/efo/EFO_1001331 GCST90041851 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peripheral vascular disease 4,301 European ancestry cases, 52,336 European ancestry controls NA Affymetrix [11397842] (imputed) 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90086136 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Peripheral vascular disease 4,301 European ancestry cases, 52,336 European ancestry controls NA Affymetrix [15468298] (imputed) 3 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90086137 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - buscopan 10mg tablet (UKB data field 20003_1140865396) 432 European ancestry cases, 455,844 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042007 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - peppermint oil product (UKB data field 20003_1140865414) 222 European ancestry cases, 456,054 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042008 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - colpermin 0.2ml m/r gel e/c capsule (UKB data field 20003_1140865416) 405 European ancestry cases, 455,871 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042009 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cimetidine (UKB data field 20003_1140865426) 353 European ancestry cases, 455,923 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042010 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - imodium 2mg capsule (UKB data field 20003_1140865564) 234 European ancestry cases, 456,042 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042011 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mesalazine (UKB data field 20003_1140865578) 636 European ancestry cases, 455,640 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042012 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - asacol 400mg e/c tablet (UKB data field 20003_1140865580) 621 European ancestry cases, 455,655 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042013 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pentasa sr 250mg m/r tablet (UKB data field 20003_1140865588) 292 European ancestry cases, 455,984 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042014 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - omeprazole (UKB data field 20003_1140865634) 26,869 European ancestry cases, 429,407 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042015 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - codeine phosphate+kaolin 10mg/3g/10ml mixture (UKB data field 20003_1140865654) 154 European ancestry cases, 456,122 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042016 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sulphasalazine (UKB data field 20003_1140865668) 233 European ancestry cases, 456,043 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042017 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salazopyrin 500mg tablet (UKB data field 20003_1140865670) 261 European ancestry cases, 456,015 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042018 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bone cancer (PheCode 170.1) 121 European ancestry cases, 456,227 European ancestry controls NA NR [11842647] (imputed) 0 bone neoplasm http://www.ebi.ac.uk/efo/EFO_0003820 GCST90041824 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of connective tissue (PheCode 170.2) 319 European ancestry cases, 456,029 European ancestry controls NA NR [11842647] (imputed) 0 connective tissue neoplasm http://purl.obolibrary.org/obo/MONDO_0021581 GCST90041825 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Handedness (chirality/laterality): Right-handed (UKB data field 1707_1) 404,974 European ancestry cases, 50,989 European ancestry controls NA NR [11842647] (imputed) 0 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST90041826 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Handedness (chirality/laterality): Left-handed (UKB data field 1707_2) 43,292 European ancestry cases, 412,671 European ancestry controls NA NR [11842647] (imputed) 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90041827 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Handedness (chirality/laterality): Use both right and left hands equally (UKB data field 1707_3) 7,697 European ancestry cases, 448,266 European ancestry controls NA NR [11842647] (imputed) 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90041828 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Melanomas of skin (PheCode 172.11) 2,824 European ancestry cases, 453,524 European ancestry controls NA NR [11842647] (imputed) 1 cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0000389 GCST90041829 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other non-epithelial cancer of skin (PheCode 172.2) 11,964 European ancestry cases, 444,384 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90041830 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Carcinoma in situ of skin (PheCode 172.3) 573 European ancestry cases, 455,775 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90041831 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neoplasm of uncertain behavior of skin (PheCode 173) 184 European ancestry cases, 456,164 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90041832 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of female breast (PheCode 174.11) 10,971 European ancestry cases, 445,377 European ancestry controls NA NR [11842647] (imputed) 1 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90041833 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breast cancer [female] (PheCode 174.1) 1,830 European ancestry cases, 454,518 European ancestry controls NA NR [11842647] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90041834 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neoplasm of uncertain behavior of breast (PheCode 174.3) 111 European ancestry cases, 247,429 European ancestry controls NA NR [11842647] (imputed) 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90041835 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair colour (natural, before greying): Blonde (UKB data field 1747_1) 51,424 European ancestry cases, 403,740 European ancestry controls NA NR [11842647] (imputed) 44 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90041836 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Diabetes (UKB data field 20107_9) 37,943 European ancestry cases, 357,277 European ancestry controls NA NR [11842647] (imputed) 1 diabetes mellitus, family history http://www.ebi.ac.uk/efo/EFO_0000400, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042676 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Heart disease (UKB data field 20110_1) 84,417 European ancestry cases, 335,864 European ancestry controls NA NR [11842647] (imputed) 0 family history, heart disease http://www.ebi.ac.uk/efo/EFO_0000493, http://www.ebi.ac.uk/efo/EFO_0003777 GCST90042677 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Alzheimer's disease/dementia (UKB data field 20110_10) 36,155 European ancestry cases, 381,650 European ancestry controls NA NR [11842647] (imputed) 3 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90042678 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: PHESANT recoding (UKB data field 20110_100) 173,897 European ancestry cases, 245,881 European ancestry controls NA NR [11842647] (imputed) 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042679 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: PHESANT recoding (UKB data field 20110_101) 325,547 European ancestry cases, 96,532 European ancestry controls NA NR [11842647] (imputed) 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042680 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Parkinson's disease (UKB data field 20110_11) 6,877 European ancestry cases, 409,676 European ancestry controls NA NR [11842647] (imputed) 0 family history, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0000493, http://purl.obolibrary.org/obo/MONDO_0005180 GCST90042681 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Severe depression (UKB data field 20110_12) 27,823 European ancestry cases, 389,470 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, family history http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042682 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Stroke (UKB data field 20110_2) 60,152 European ancestry cases, 358,865 European ancestry controls NA NR [11842647] (imputed) 0 stroke, family history http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042683 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Lung cancer (UKB data field 20110_3) 17,376 European ancestry cases, 399,956 European ancestry controls NA NR [11842647] (imputed) 0 family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0006953 GCST90042684 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Bowel cancer (UKB data field 20110_4) 21,763 European ancestry cases, 395,445 European ancestry controls NA NR [11842647] (imputed) 0 intestinal cancer, family history http://www.ebi.ac.uk/efo/EFO_0007330, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042685 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Breast cancer (UKB data field 20110_5) 34,581 European ancestry cases, 382,951 European ancestry controls NA NR [11842647] (imputed) 1 family history of breast cancer http://www.ebi.ac.uk/efo/EFO_0005606 GCST90042686 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Chronic bronchitis/emphysema (UKB data field 20110_6) 25,054 European ancestry cases, 392,709 European ancestry controls NA NR [11842647] (imputed) 0 emphysema, family history, chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0000464, http://www.ebi.ac.uk/efo/EFO_0000493, http://www.ebi.ac.uk/efo/EFO_0006505 GCST90042687 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: High blood pressure (UKB data field 20110_8) 128,883 European ancestry cases, 291,510 European ancestry controls NA NR [11842647] (imputed) 0 hypertension, family history http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042688 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of mother: Diabetes (UKB data field 20110_9) 39,259 European ancestry cases, 378,667 European ancestry controls NA NR [11842647] (imputed) 0 diabetes mellitus, family history http://www.ebi.ac.uk/efo/EFO_0000400, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042689 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Heart disease (UKB data field 20111_1) 37,330 European ancestry cases, 320,951 European ancestry controls NA NR [11842647] (imputed) 0 family history, heart disease http://www.ebi.ac.uk/efo/EFO_0000493, http://www.ebi.ac.uk/efo/EFO_0003777 GCST90042690 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Alzheimer's disease/dementia (UKB data field 20111_10) 2,087 European ancestry cases, 353,955 European ancestry controls NA NR [11842647] (imputed) 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90042691 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: PHESANT recoding (UKB data field 20111_100) 242,117 European ancestry cases, 117,573 European ancestry controls NA NR [11842647] (imputed) 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042692 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: PHESANT recoding (UKB data field 20111_101) 305,084 European ancestry cases, 58,273 European ancestry controls NA NR [11842647] (imputed) 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042693 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Parkinson's disease (UKB data field 20111_11) 1,976 European ancestry cases, 353,999 European ancestry controls NA NR [11842647] (imputed) 0 family history, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0000493, http://purl.obolibrary.org/obo/MONDO_0005180 GCST90042694 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Severe depression (UKB data field 20111_12) 25,919 European ancestry cases, 331,152 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, family history http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042695 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Prostate cancer (UKB data field 20111_13) 5,873 European ancestry cases, 350,300 European ancestry controls NA NR [11842647] (imputed) 0 prostate cancer, family history http://purl.obolibrary.org/obo/MONDO_0008315, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042696 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Stroke (UKB data field 20111_2) 11,878 European ancestry cases, 344,813 European ancestry controls NA NR [11842647] (imputed) 0 stroke, family history http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042697 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Lung cancer (UKB data field 20111_3) 8,126 European ancestry cases, 348,227 European ancestry controls NA NR [11842647] (imputed) 0 family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0006953 GCST90042698 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Bowel cancer (UKB data field 20111_4) 8,807 European ancestry cases, 347,473 European ancestry controls NA NR [11842647] (imputed) 0 intestinal cancer, family history http://www.ebi.ac.uk/efo/EFO_0007330, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042699 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Breast cancer (UKB data field 20111_5) 16,344 European ancestry cases, 340,229 European ancestry controls NA NR [11842647] (imputed) 0 family history of breast cancer http://www.ebi.ac.uk/efo/EFO_0005606 GCST90042700 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Severity of problems due to mania or irritability - Needed treatment or caused problems with work relationships finances the law or other aspects of life (UKB data field 20493) 10,020 European ancestry cases, 23,711 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90042801 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever sought or received professional help for mental distress (UKB data field 20499) 57,861 European ancestry cases, 89,409 European ancestry controls NA NR [11842647] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90042802 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leukemia (PheCode 204) 147 European ancestry cases, 456,201 European ancestry controls NA NR [11842647] (imputed) 0 leukemia http://www.ebi.ac.uk/efo/EFO_0000565 GCST90042803 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever suffered mental distress preventing usual activities (UKB data field 20500) 48,729 European ancestry cases, 97,076 European ancestry controls NA NR [11842647] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90042804 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had period of mania excitability (UKB data field 20501) 6,175 European ancestry cases, 138,155 European ancestry controls NA NR [11842647] (imputed) 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90042805 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had period extreme irritability (UKB data field 20502) 37,643 European ancestry cases, 105,548 European ancestry controls NA NR [11842647] (imputed) 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90042806 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever addicted to prescription or over the counter medication (UKB data field 20503) 1,240 European ancestry cases, 7,443 European ancestry controls NA NR [11842647] (imputed) 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90042807 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Been in serious accident believed to be life-threatening (UKB data field 20526) 14,315 European ancestry cases, 133,267 European ancestry controls NA NR [11842647] (imputed) 0 injury, trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0000546, http://www.ebi.ac.uk/efo/EFO_0010703 GCST90042808 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Been involved in combat or exposed to war-zone (UKB data field 20527) 5,104 European ancestry cases, 142,512 European ancestry controls NA NR [11842647] (imputed) 0 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST90042809 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diagnosed with life threatening illness - Never (UKB data field 20528) 24,038 European ancestry cases, 123,147 European ancestry controls NA NR [11842647] (imputed) 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90042810 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Victim of physically violent crime (UKB data field 20529) 27,818 European ancestry cases, 119,667 European ancestry controls NA NR [11842647] (imputed) 0 injury, trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0000546, http://www.ebi.ac.uk/efo/EFO_0010703 GCST90042811 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Witnessed sudden violent death (UKB data field 20530) 19,937 European ancestry cases, 127,580 European ancestry controls NA NR [11842647] (imputed) 0 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST90042812 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Victim of sexual assault (UKB data field 20531) 21,795 European ancestry cases, 124,182 European ancestry controls NA NR [11842647] (imputed) 0 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST90042813 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sleep change (UKB data field 20532) 57,215 European ancestry cases, 14,471 European ancestry controls NA NR [11842647] (imputed) 0 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST90042814 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Trouble falling asleep (UKB data field 20533) 43,474 European ancestry cases, 13,741 European ancestry controls NA NR [11842647] (imputed) 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90042815 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sleeping too much (UKB data field 20534) 11,833 European ancestry cases, 45,382 European ancestry controls NA NR [11842647] (imputed) 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90042816 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Waking too early (UKB data field 20535) 43,398 European ancestry cases, 13,817 European ancestry controls NA NR [11842647] (imputed) 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90042817 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Weight change during worst episode of depression: Stayed about the same or was on a diet (UKB data field 20536_0) 28,708 European ancestry cases, 42,377 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, body weight http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004338 GCST90042818 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Weight change during worst episode of depression: Gained weight (UKB data field 20536_1) 12,349 European ancestry cases, 58,736 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, body weight http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004338 GCST90042819 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Weight change during worst episode of depression: Lost weight (UKB data field 20536_2) 25,498 European ancestry cases, 45,587 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, body weight http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004338 GCST90042820 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Weight change during worst episode of depression: Both gained and lost some weight during the episode (UKB data field 20536_3) 4,530 European ancestry cases, 66,555 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, body weight http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004338 GCST90042821 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worried most days during period of worst anxiety (UKB data field 20538) 38,994 European ancestry cases, 5,170 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90042822 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Multiple worries during worst period of anxiety (UKB data field 20540) 33,257 European ancestry cases, 10,683 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90042823 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Difficulty stopping worrying during worst period of anxiety (UKB data field 20541) 41,931 European ancestry cases, 2,607 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90042824 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Stronger worrying than other people during period of worst anxiety (UKB data field 20542) 25,942 European ancestry cases, 5,550 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90042825 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Chronic bronchitis/emphysema (UKB data field 20111_6) 10,227 European ancestry cases, 346,364 European ancestry controls NA NR [11842647] (imputed) 0 emphysema, family history, chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0000464, http://www.ebi.ac.uk/efo/EFO_0000493, http://www.ebi.ac.uk/efo/EFO_0006505 GCST90042701 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: High blood pressure (UKB data field 20111_8) 75,869 European ancestry cases, 283,494 European ancestry controls NA NR [11842647] (imputed) 0 hypertension, family history http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042702 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of siblings: Diabetes (UKB data field 20111_9) 30,458 European ancestry cases, 327,103 European ancestry controls NA NR [11842647] (imputed) 0 diabetes mellitus, family history http://www.ebi.ac.uk/efo/EFO_0000400, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042703 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Smoking status: Never (UKB data field 20116_0) 245,064 European ancestry cases, 209,365 European ancestry controls NA NR [11842647] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90042704 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Smoking status: Previous (UKB data field 20116_1) 161,807 European ancestry cases, 292,622 European ancestry controls NA NR [11842647] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90042705 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Smoking status: Current (UKB data field 20116_2) 47,558 European ancestry cases, 406,871 European ancestry controls NA NR [11842647] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90042706 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcohol drinker status: Never (UKB data field 20117_0) 14,532 European ancestry cases, 441,123 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042707 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcohol drinker status: Previous (UKB data field 20117_1) 15,997 European ancestry cases, 439,658 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042708 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcohol drinker status: Current (UKB data field 20117_2) 425,126 European ancestry cases, 30,529 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042709 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: Scotland - Large Urban Area (UKB data field 20118_11) 25,864 European ancestry cases, 426,040 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042710 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: Scotland - Other Urban Area (UKB data field 20118_12) 4,903 European ancestry cases, 447,001 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042711 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: Scotland - Accessible Small Town (UKB data field 20118_13) 1,333 European ancestry cases, 450,571 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042712 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: Scotland - Accessible Rural (UKB data field 20118_16) 1,512 European ancestry cases, 450,392 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042713 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: England/Wales - Urban - less sparse (UKB data field 20118_5) 354,804 European ancestry cases, 97,100 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042714 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: England/Wales - Town and Fringe - less sparse (UKB data field 20118_6) 31,418 European ancestry cases, 420,486 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042715 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: England/Wales - Village - less sparse (UKB data field 20118_7) 22,265 European ancestry cases, 429,639 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042716 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Home area population density - urban or rural: England/Wales - Hamlet and Isolated Dwelling - less sparse (UKB data field 20118_8) 9,753 European ancestry cases, 442,151 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90042717 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bipolar and major depression status: No Bipolar or Depression (UKB data field 20126_0) 78,501 European ancestry cases, 30,280 European ancestry controls NA NR [11842647] (imputed) 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90042718 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bipolar and major depression status: Bipolar I Disorder (UKB data field 20126_1) 702 European ancestry cases, 108,079 European ancestry controls NA NR [11842647] (imputed) 0 bipolar I disorder http://www.ebi.ac.uk/efo/EFO_0009963 GCST90042719 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bipolar and major depression status: Bipolar II Disorder (UKB data field 20126_2) 645 European ancestry cases, 108,136 European ancestry controls NA NR [11842647] (imputed) 0 bipolar II disorder http://www.ebi.ac.uk/efo/EFO_0009964 GCST90042720 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bipolar and major depression status: Probable Recurrent major depression (severe) (UKB data field 20126_3) 7,924 European ancestry cases, 100,857 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90042721 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bipolar and major depression status: Probable Recurrent major depression (moderate) (UKB data field 20126_4) 13,711 European ancestry cases, 95,070 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90042722 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bipolar and major depression status: Single Probable major depression episode (UKB data field 20126_5) 7,298 European ancestry cases, 101,483 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90042723 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reproduciblity of spirometry measurement using ERS ATS criteria (UKB data field 20152) 267,438 European ancestry cases, 75,078 European ancestry controls NA NR [11842647] (imputed) 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90042724 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever smoked (UKB data field 20160) 276,380 European ancestry cases, 178,101 European ancestry controls NA NR [11842647] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90042725 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symbol digit completion status: PHESANT recoding (UKB data field 20245_2) 2,405 European ancestry cases, 110,657 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042751 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Trail making completion status: PHESANT recoding (UKB data field 20246_0) 98,089 European ancestry cases, 15,228 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042752 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Trail making completion status: PHESANT recoding (UKB data field 20246_1) 4,596 European ancestry cases, 108,721 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042753 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Trail making completion status: PHESANT recoding (UKB data field 20246_2) 2,979 European ancestry cases, 110,338 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042754 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Trail making completion status: PHESANT recoding (UKB data field 20246_3) 7,653 European ancestry cases, 105,664 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042755 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Guilty feelings (UKB data field 2030) 127,374 European ancestry cases, 317,007 European ancestry controls NA NR [11842647] (imputed) 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90042756 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Lymphoid leukemia, chronic (PheCode 204.12) 356 European ancestry cases, 455,992 European ancestry controls NA NR [11842647] (imputed) 0 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90042757 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Myeloid leukemia, acute (PheCode 204.21) 312 European ancestry cases, 456,036 European ancestry controls NA NR [11842647] (imputed) 0 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST90042758 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Myeloid leukemia, chronic (PheCode 204.22) 144 European ancestry cases, 456,204 European ancestry controls NA NR [11842647] (imputed) 0 chronic myelogenous leukemia http://www.ebi.ac.uk/efo/EFO_0000339 GCST90042759 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Multiple myeloma (PheCode 204.4) 564 European ancestry cases, 455,784 European ancestry controls NA NR [11842647] (imputed) 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90042760 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Risk taking (UKB data field 2040) 115,248 European ancestry cases, 324,830 European ancestry controls NA NR [11842647] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90042761 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever addicted to any substance or behaviour (UKB data field 20401) 8,803 European ancestry cases, 137,303 European ancestry controls NA NR [11842647] (imputed) 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90042762 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had known person concerned about, or recommend reduction of, alcohol consumption: No (UKB data field 20405_0) 134,738 European ancestry cases, 12,807 European ancestry controls NA NR [11842647] (imputed) 0 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST90042763 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had known person concerned about, or recommend reduction of, alcohol consumption: Yes, but not in the last year (UKB data field 20405_1) 6,736 European ancestry cases, 140,809 European ancestry controls NA NR [11842647] (imputed) 0 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST90042764 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had known person concerned about, or recommend reduction of, alcohol consumption: Yes, during the last year (UKB data field 20405_2) 6,071 European ancestry cases, 141,474 European ancestry controls NA NR [11842647] (imputed) 0 longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007645 GCST90042765 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever addicted to alcohol (UKB data field 20406) 3,406 European ancestry cases, 4,757 European ancestry controls NA NR [11842647] (imputed) 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90042766 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever been injured or injured someone else through drinking alcohol: No (UKB data field 20411_0) 141,400 European ancestry cases, 6,284 European ancestry controls NA NR [11842647] (imputed) 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90042767 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever been injured or injured someone else through drinking alcohol: Yes, but not in the last year (UKB data field 20411_1) 5,608 European ancestry cases, 142,076 European ancestry controls NA NR [11842647] (imputed) 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90042768 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever been injured or injured someone else through drinking alcohol: Yes, during the last year (UKB data field 20411_2) 676 European ancestry cases, 147,008 European ancestry controls NA NR [11842647] (imputed) 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90042769 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tense, sore or aching muscles during worst period of anxiety (UKB data field 20417) 16,421 European ancestry cases, 25,331 European ancestry controls NA NR [11842647] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90042770 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Difficulty concentrating during worst period of anxiety (UKB data field 20419) 33,078 European ancestry cases, 10,647 European ancestry controls NA NR [11842647] (imputed) 0 decreased concentration http://purl.obolibrary.org/obo/PATO_0001163 GCST90042771 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever felt worried tense or anxious for most of a month or longer (UKB data field 20421) 36,774 European ancestry cases, 101,198 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90042772 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. More irritable than usual during worst period of anxiety (UKB data field 20422) 30,168 European ancestry cases, 11,743 European ancestry controls NA NR [11842647] (imputed) 0 irritability measurement http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042773 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Keyed up or on edge during worst period of anxiety (UKB data field 20423) 34,643 European ancestry cases, 8,992 European ancestry controls NA NR [11842647] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90042774 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever worried more than most people would in similar situation (UKB data field 20425) 32,152 European ancestry cases, 91,671 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90042775 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Restless during period of worst anxiety (UKB data field 20426) 25,526 European ancestry cases, 16,935 European ancestry controls NA NR [11842647] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90042776 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Frequent trouble falling or staying asleep during worst period of anxiety (UKB data field 20427) 36,531 European ancestry cases, 8,092 European ancestry controls NA NR [11842647] (imputed) 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90042777 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Professional informed about anxiety (UKB data field 20428) 27,846 European ancestry cases, 17,723 European ancestry controls NA NR [11842647] (imputed) 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90042778 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Easily tired during worst period of anxiety (UKB data field 20429) 30,740 European ancestry cases, 12,049 European ancestry controls NA NR [11842647] (imputed) 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90042779 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever addicted to a behaviour or miscellanous (UKB data field 20431) 2,065 European ancestry cases, 6,619 European ancestry controls NA NR [11842647] (imputed) 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90042780 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Difficulty concentrating during worst depression (UKB data field 20435) 58,120 European ancestry cases, 15,609 European ancestry controls NA NR [11842647] (imputed) 0 decreased concentration http://purl.obolibrary.org/obo/PATO_0001163 GCST90042781 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Thoughts of death during worst depression (UKB data field 20437) 41,009 European ancestry cases, 37,694 European ancestry controls NA NR [11842647] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90042782 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had prolonged loss of interest in normal activities (UKB data field 20441) 58,298 European ancestry cases, 89,047 European ancestry controls NA NR [11842647] (imputed) 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90042783 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Depression possibly related to childbirth (UKB data field 20445) 6,107 European ancestry cases, 42,012 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90042784 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had prolonged feelings of sadness or depression (UKB data field 20446) 80,825 European ancestry cases, 66,571 European ancestry controls NA NR [11842647] (imputed) 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90042785 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Depression possibly related to stressful or traumatic event (UKB data field 20447) 60,952 European ancestry cases, 22,384 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90042786 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Professional informed about depression (UKB data field 20448) 53,752 European ancestry cases, 29,524 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90042787 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Feelings of tiredness during worst episode of depression (UKB data field 20449) 61,542 European ancestry cases, 13,461 European ancestry controls NA NR [11842647] (imputed) 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90042788 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Feelings of worthlessness during worst period of depression (UKB data field 20450) 39,787 European ancestry cases, 38,213 European ancestry controls NA NR [11842647] (imputed) 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90042789 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever addicted to illicit or recreational drugs (UKB data field 20456) 682 European ancestry cases, 8,023 European ancestry controls NA NR [11842647] (imputed) 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90042790 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever heard an unreal voice (UKB data field 20463) 2,585 European ancestry cases, 144,493 European ancestry controls NA NR [11842647] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90042791 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever prescribed a medication for unusual or psychotic experiences (UKB data field 20466) 809 European ancestry cases, 6,438 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042792 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever believed in an unreal conspiracy against self (UKB data field 20468) 1,165 European ancestry cases, 146,241 European ancestry controls NA NR [11842647] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90042793 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever seen an unreal vision (UKB data field 20471) 4,728 European ancestry cases, 141,448 European ancestry controls NA NR [11842647] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90042794 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever believed in unreal communications or signs (UKB data field 20474) 1,050 European ancestry cases, 146,282 European ancestry controls NA NR [11842647] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90042795 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever talked to a health professional about unusual or psychotic experiences (UKB data field 20477) 1,543 European ancestry cases, 5,718 European ancestry controls NA NR [11842647] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90042796 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever self harmed (UKB data field 20480) 6,390 European ancestry cases, 140,943 European ancestry controls NA NR [11842647] (imputed) 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90042797 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Self harmed in past year (UKB data field 20481) 547 European ancestry cases, 5,818 European ancestry controls NA NR [11842647] (imputed) 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90042798 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever attempted suicide (UKB data field 20483) 3,288 European ancestry cases, 2,895 European ancestry controls NA NR [11842647] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90042799 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Contemplated self harm in past year (UKB data field 20486) 4,320 European ancestry cases, 17,326 European ancestry controls NA NR [11842647] (imputed) 0 self-injurious ideation http://www.ebi.ac.uk/efo/EFO_0010817 GCST90042800 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI1 numeric addition test - 14 (20165) 112,934 European ancestry cases, 2,938 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042726 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI2 identify largest number - 987 (UKB data field 20167) 114,880 European ancestry cases, 1,017 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042727 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI3 word interpolation - grow (UKB data field 20169) 96,755 European ancestry cases, 19,113 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042728 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI4 positional arithmetic - 5 (UKB data field 20171) 102,666 European ancestry cases, 12,637 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042729 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI5 family relationship calculation - aunt (UKB data field 20173) 63,006 European ancestry cases, 50,078 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042730 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI6 conditional arithmetic - 68 (UKB data field 20175) 76,736 European ancestry cases, 25,109 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042731 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI7 synonym - pause (UKB data field 20177) 77,748 European ancestry cases, 5,425 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042732 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI8 chained arithmetic - 25 (UKB data field 20179) 57,499 European ancestry cases, 18,257 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042733 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI9 concept interpolation - long (UKB data field 20181) 20,381 European ancestry cases, 10,614 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042734 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI10 arithmetic sequence recognition - 96 (UKB data field 20183) 17,106 European ancestry cases, 3,495 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042735 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI11 antonym - anxious (UKB data field 20185) 7,120 European ancestry cases, 2,458 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042736 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cognitive function - FI12 square sequence recognition - 50 (UKB data field 20187) 2,610 European ancestry cases, 3,542 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90042737 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hodgkin's disease (PheCode 201) 215 European ancestry cases, 456,133 European ancestry controls NA NR [11842647] (imputed) 0 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST90042738 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nodular lymphoma (PheCode 202.21) 394 European ancestry cases, 455,954 European ancestry controls NA NR [11842647] (imputed) 0 follicular lymphoma http://purl.obolibrary.org/obo/MONDO_0018906 GCST90042739 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Large cell lymphoma (PheCode 202.24) 603 European ancestry cases, 455,745 European ancestry controls NA NR [11842647] (imputed) 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90042740 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-Hodgkins lymphoma (PheCode 202.2) 1,395 European ancestry cases, 454,953 European ancestry controls NA NR [11842647] (imputed) 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90042741 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Loneliness (UKB data field 2020) 81,011 European ancestry cases, 367,945 European ancestry controls NA NR [11842647] (imputed) 0 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST90042742 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fluid intelligence completion status: PHESANT recoding (UKB data field 20242_0) 101,835 European ancestry cases, 14,468 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042743 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fluid intelligence completion status: PHESANT recoding (UKB data field 20242_1) 3,362 European ancestry cases, 112,941 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042744 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fluid intelligence completion status: PHESANT recoding (UKB data field 20242_2) 11,106 European ancestry cases, 105,197 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042745 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pairs matching completion status: PHESANT recoding (UKB data field 20244_0) 104,064 European ancestry cases, 7,494 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042746 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pairs matching completion status: PHESANT recoding (UKB data field 20244_1) 3,501 European ancestry cases, 108,057 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042747 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pairs matching completion status: PHESANT recoding (UKB data field 20244_2) 3,993 European ancestry cases, 107,565 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042748 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symbol digit completion status: PHESANT recoding (UKB data field 20245_0) 108,439 European ancestry cases, 4,623 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042749 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symbol digit completion status: PHESANT recoding (UKB data field 20245_1) 2,218 European ancestry cases, 110,844 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042750 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (processing speed) x major depressive disorder interaction (1df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 16 unipolar depression, information processing speed, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096937 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (processing speed) x major depressive disorder interaction (2df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 46 unipolar depression, information processing speed, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096938 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (global cognition) 9,567 European ancestry individuals NA NR [NR] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096939 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (global cognition) x major depressive disorder interaction (1df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 3 unipolar depression, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096940 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (global cognition) x major depressive disorder interaction (2df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 8 unipolar depression, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096941 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (immediate memory) 9,567 European ancestry individuals NA NR [NR] (imputed) 0 memory performance, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0004874, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096942 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (immediate memory) x major depressive disorder interaction (1df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 0 unipolar depression, memory performance, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004874, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096943 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (immediate memory) x major depressive disorder interaction (2df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 0 unipolar depression, memory performance, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004874, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096944 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (executive function) 9,567 European ancestry individuals NA NR [NR] (imputed) 3 executive function measurement, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0009332, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096930 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (executive function) x major depressive disorder interaction (1df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 18 executive function measurement, unipolar depression, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0009332, http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096931 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (executive function) x major depressive disorder interaction (2df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 32 executive function measurement, unipolar depression, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0009332, http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096932 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (delayed memory) 9,567 European ancestry individuals NA NR [NR] (imputed) 1 word list delayed recall measurement, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0006805, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096933 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (delayed memory) x major depressive disorder interaction (1df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 0 unipolar depression, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096934 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (delayed memory) x major depressive disorder interaction (2df) 3,510 European ancestry major depressive disorder cases, 6,057 European ancestry major depressive disorder controls NA NR [NR] (imputed) 2 unipolar depression, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096935 Genome-wide genotyping array 2022-03-28 34782712 Thalamuthu A 2021-11-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34782712 Genome-wide interaction study with major depression identifies novel variants associated with cognitive function. Cognitive function (processing speed) 9,567 European ancestry individuals NA NR [NR] (imputed) 6 information processing speed, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90096936 Genome-wide genotyping array 2022-04-22 34115965 Kosmicki JA 2021-06-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34115965 Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. COVID-19 1,146 African ancestry cases, 21,959 African ancestry controls, 88 Admixed American cases, 1,307 Admixed American controls, 80 East Asian ancestry cases, 2,085 East Asian ancestry controls, 18,920 European ancestry cases, 530,629 European ancestry controls, 718 South Asian ancestry cases, 9,225 South Asian ancestry controls NA NR [7000000] 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90093364 Exome-wide sequencing 2022-04-22 34115965 Kosmicki JA 2021-06-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34115965 Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. COVID-19 (covid vs negative) 1,146 African ancestry cases, 3,854 African ancestry controls, 88 Admixed American cases, 306 Admixed American controls, 80 East Asian ancestry cases, 161 East Asian ancestry controls, 18,920 European ancestry cases, 69,283 European ancestry controls, 718 South Asian ancestry cases, 1,030 South Asian ancestry controls NA NR [7000000] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90093365 Exome-wide sequencing 2022-04-22 34115965 Kosmicki JA 2021-06-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34115965 Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. COVID-19 (hospitalized vs population) 302 African ancestry cases, 18,909 African ancestry controls, 4,478 European ancestry cases, 530,629 European ancestry controls, 148 South Asian ancestry cases, 9,225 South Asian ancestry controls NA NR [7000000] 3 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90093366 Exome-wide sequencing 2022-04-22 34115965 Kosmicki JA 2021-06-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34115965 Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. COVID-19 (severe vs population) 72 African ancestry cases, 18,909 African ancestry controls, 1,203 European ancestry cases, 500,624 European ancestry controls, 29 South Asian ancestry cases, 9,225 South Asian ancestry controls NA NR [7000000] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90093367 Exome-wide sequencing 2022-04-22 34115965 Kosmicki JA 2021-06-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34115965 Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. COVID-19 (hospitalized vs not hospitalized) 302 African ancestry cases, 716 African ancestry controls, 4,478 European ancestry cases, 14,442 European ancestry controls, 148 South Asian ancestry cases, 570 South Asian ancestry controls NA NR [7000000] 0 COVID-19 symptoms measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0600019, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90101884 Exome-wide sequencing 2022-04-22 34115965 Kosmicki JA 2021-06-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34115965 Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. COVID-19 (not hospitalized vs population) 828 African ancestry cases, 21,959 African ancestry controls, 80 Admixed American cases, 1,307 Admixed American controls, 59 East Asian ancestry cases, 2,085 East Asian ancestry controls, 14,442 European ancestry cases, 530,629 European ancestry controls, 570 South Asian ancestry cases, 9,225 South Asian ancestry controls NA NR [7000000] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90101885 Exome-wide sequencing 2022-04-22 34115965 Kosmicki JA 2021-06-03 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34115965 Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. COVID-19 (severe vs not hospitalized) 72 African ancestry cases, 716 African ancestry controls, 1,203 European ancestry cases, 14,229 European ancestry controls, 29 South Asian ancestry cases, 570 South Asian ancestry controls NA NR [7000000] 0 COVID-19 symptoms measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0600019, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90101886 Exome-wide sequencing 2022-03-15 34743558 Zekavat SM 2021-11-08 Circulation www.ncbi.nlm.nih.gov/pubmed/34743558 Deep Learning of the Retina Enables Phenome- and Genome-wide Analyses of the Microvasculature. Retinal vascular fractal dimension 38,932 British ancestry individuals NA Affymetrix [15580782] (imputed) 149 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90095200 Genome-wide genotyping array 2022-03-15 34743558 Zekavat SM 2021-11-08 Circulation www.ncbi.nlm.nih.gov/pubmed/34743558 Deep Learning of the Retina Enables Phenome- and Genome-wide Analyses of the Microvasculature. Retinal vascular fractal density 38,932 British ancestry individuals NA Affymetrix [15580782] (imputed) 168 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90095201 Genome-wide genotyping array 2022-03-30 33311554 Jiang X 2020-12-11 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33311554 Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants. Corneal resistance factor 76,029 white-British ancestry individuals 10,130 non white-British ancestry individuals Affymetrix [11014269] (imputed) 251 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST90100568 Genome-wide genotyping array 2022-05-13 34852423 Kim YA 2021-12-02 Endocrinol Metab (Seoul) www.ncbi.nlm.nih.gov/pubmed/34852423 Unveiling Genetic Variants Underlying Vitamin D Deficiency in Multiple Korean Cohorts by a Genome-Wide Association Study. Vitamin D insufficiency 7,590 Korean ancestry individuals NA Affymetrix [1695891] (imputed) 10 vitamin D deficiency http://www.ebi.ac.uk/efo/EFO_0003762 GCST90101732 Genome-wide genotyping array 2022-02-28 34854908 Veluchamy A 2021-12-01 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/34854908 Association of Genetic Variant at Chromosome 12q23.1 With Neuropathic Pain Susceptibility. Neuropathic pain 4,512 European ancestry cases, 428,489 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 17 neuropathic pain http://www.ebi.ac.uk/efo/EFO_0005762 GCST90095046 Genome-wide genotyping array 2022-03-08 35165267 Boua PR 2022-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35165267 Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans. Carotid Intima-media thickness (mean of the maximum cIMT) 7,894 Sub-Saharan African ancestry individuals NA Illumina [13900000] (imputed) 77 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90092502 Genome-wide genotyping array 2022-03-08 35165267 Boua PR 2022-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35165267 Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans. Carotid Intima-media thickness (mean of the maximum cIMT) 3,963 Sub-Saharan African ancestry females NA Illumina [13900000] (imputed) 86 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90092503 Genome-wide genotyping array 2022-03-08 35165267 Boua PR 2022-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35165267 Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans. Carotid Intima-media thickness (mean of the maximum cIMT) 3,931 Sub-Saharan African ancestry males NA Illumina [13900000] (imputed) 79 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90092504 Genome-wide genotyping array 2022-03-08 35165267 Boua PR 2022-02-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35165267 Genetic associations with carotid intima-media thickness link to atherosclerosis with sex-specific effects in sub-Saharan Africans. Carotid Intima-media thickness (mean of the maximum cIMT) 3,963 Sub-Saharan African ancestry females, 3,931 Sub-Saharan African ancestry males NA Illumina [7666802] (imputed) 36 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90092505 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - persantin 25mg tablet (UKB data field 20003_1140861780) 271 European ancestry cases, 456,005 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041957 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - aspirin 75mg tablet (UKB data field 20003_1140861806) 2,683 European ancestry cases, 453,593 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041958 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bezafibrate (UKB data field 20003_1140861924) 418 European ancestry cases, 455,858 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041959 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - questran 4g/sachet powder (UKB data field 20003_1140861936) 137 European ancestry cases, 456,139 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041960 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fenofibrate (UKB data field 20003_1140861954) 607 European ancestry cases, 455,669 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041961 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - simvastatin (UKB data field 20003_1140861958) 51,682 European ancestry cases, 404,594 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041962 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ventolin 100micrograms inhaler (UKB data field 20003_1140861998) 13,081 European ancestry cases, 443,195 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041963 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ventolin 2mg tablet (UKB data field 20003_1140862060) 175 European ancestry cases, 456,101 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041964 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salamol 100micrograms inhaler (UKB data field 20003_1140862086) 1,397 European ancestry cases, 454,879 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041965 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salmeterol (UKB data field 20003_1140862144) 1,199 European ancestry cases, 455,077 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041966 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - serevent 25mcg inhaler (UKB data field 20003_1140862148) 1,226 European ancestry cases, 455,050 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041967 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bricanyl 250mcg inhaler (UKB data field 20003_1140862168) 1,027 European ancestry cases, 455,249 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041968 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - atrovent 20micrograms inhaler (UKB data field 20003_1140862236) 478 European ancestry cases, 455,798 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041969 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - phyllocontin continus 225mg m/r tablet (UKB data field 20003_1140862266) 161 European ancestry cases, 456,115 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041970 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - becloforte 250micrograms inhaler (UKB data field 20003_1140862380) 252 European ancestry cases, 456,024 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041971 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - becotide 50 inhaler (UKB data field 20003_1140862382) 2,780 European ancestry cases, 453,496 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041972 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - uniphyllin continus 200mg m/r tablet (UKB data field 20003_1140862438) 219 European ancestry cases, 456,057 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041973 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - beclazone 50 inhaler (UKB data field 20003_1140862476) 1,306 European ancestry cases, 454,970 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041974 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sodium cromoglycate (UKB data field 20003_1140862526) 118 European ancestry cases, 456,158 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041975 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - budesonide (UKB data field 20003_1140862572) 939 European ancestry cases, 455,337 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041976 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pulmicort ls 50micrograms inhaler (UKB data field 20003_1140862574) 691 European ancestry cases, 455,585 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041977 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - piriton 4mg tablet (UKB data field 20003_1140862628) 689 European ancestry cases, 455,587 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041978 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zirtek 10mg tablet (UKB data field 20003_1140862770) 119 European ancestry cases, 456,157 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041979 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - loratadine (UKB data field 20003_1140862772) 3,251 European ancestry cases, 453,025 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041980 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clarityn 10mg tablet (UKB data field 20003_1140862776) 386 European ancestry cases, 455,890 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041981 Genome-wide genotyping array 2022-03-22 34815687 Wu SE 2021-11-16 J Inflamm Res www.ncbi.nlm.nih.gov/pubmed/34815687 A Genome-Wide Association Study Identifies Novel Risk Loci for Sarcopenia in a Taiwanese Population. Low skeletal muscle mass index 35 Taiwanese ancestry cases, 61 Taiwanese ancestry controls NA Affymetrix [NR] 2 muscle measurement http://www.ebi.ac.uk/efo/EFO_0004515 GCST90096794 Genome-wide genotyping array 2022-03-22 34815687 Wu SE 2021-11-16 J Inflamm Res www.ncbi.nlm.nih.gov/pubmed/34815687 A Genome-Wide Association Study Identifies Novel Risk Loci for Sarcopenia in a Taiwanese Population. Low gait speed 37 Taiwanese ancestry cases, 59 Taiwanese ancestry controls NA Affymetrix [NR] 1 gait measurement http://www.ebi.ac.uk/efo/EFO_0007680 GCST90096795 Genome-wide genotyping array 2022-03-22 34815687 Wu SE 2021-11-16 J Inflamm Res www.ncbi.nlm.nih.gov/pubmed/34815687 A Genome-Wide Association Study Identifies Novel Risk Loci for Sarcopenia in a Taiwanese Population. Low hand grip strength 34 Taiwanese ancestry cases, 62 Taiwanese ancestry controls NA Affymetrix [NR] 8 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90096796 Genome-wide genotyping array 2022-04-05 34907023 Norheim KB 2021-12-01 RMD Open www.ncbi.nlm.nih.gov/pubmed/34907023 Genetic variants at the RTP4/MASP1 locus are associated with fatigue in Scandinavian patients with primary Sjögren's syndrome. Fatigue in primary Sjögren's syndrome 682 European ancestry individuals NA Illumina [4966157] (imputed) 2 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90100590 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: theme park or arcade attendant; fairground/funfair worker, snooker hall attendant, or other leisure attendants (UKB data field 22601_92263197) 116 European ancestry cases, 112,162 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043251 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: house cleaner, domestic, chambermaid, charlady (UKB data field 22601_92332985) 221 European ancestry cases, 112,057 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043252 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other cleaner including in offices, hospitals, schools, shops, warehouses, ships, aircraft, stations (UKB data field 22601_92332986) 438 European ancestry cases, 111,840 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043253 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: cleaner in restaurants, bars, pubs, hotels and other accommodation; chambermaid (UKB data field 22601_92333396) 176 European ancestry cases, 112,102 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043254 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: security guard/officer, night watchman, store detective, private detective, bodyguard, gateman, door keeper, cctv operator, patrolman (UKB data field 22601_92413455) 348 European ancestry cases, 111,930 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043255 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: school mid-day assistant, dinner or school meals supervisor or assistant, lunchtime supervisor (UKB data field 22601_92443411) 220 European ancestry cases, 112,058 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043256 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: shelf filler or stacker, stock handler, display assistant (UKB data field 22601_92513331) 527 European ancestry cases, 111,751 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043257 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other sales occupations including bill poster, ticket checker (UKB data field 22601_92593346) 204 European ancestry cases, 112,074 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043258 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Work hours - lumped category: PHESANT recoding (UKB data field 22604_1) 12,744 European ancestry cases, 81,147 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043259 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Work hours - lumped category: PHESANT recoding (UKB data field 22604_2) 19,079 European ancestry cases, 74,812 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043260 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Work hours - lumped category: PHESANT recoding (UKB data field 22604_3) 65,213 European ancestry cases, 28,678 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043261 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Work hours - lumped category: PHESANT recoding (UKB data field 22604_4) 46,380 European ancestry cases, 47,511 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043262 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very noisy: Rarely/never (UKB data field 22606_0) 86,654 European ancestry cases, 26,876 European ancestry controls NA NR [11842647] (imputed) 0 noise exposure measurement http://www.ebi.ac.uk/efo/EFO_0600015 GCST90043263 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very noisy: PHESANT recoding (UKB data field 22606_1) 64,708 European ancestry cases, 48,687 European ancestry controls NA NR [11842647] (imputed) 0 noise exposure measurement http://www.ebi.ac.uk/efo/EFO_0600015 GCST90043264 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very noisy: PHESANT recoding (UKB data field 22606_2) 22,226 European ancestry cases, 91,007 European ancestry controls NA NR [11842647] (imputed) 0 noise exposure measurement http://www.ebi.ac.uk/efo/EFO_0600015 GCST90043265 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very cold: Rarely/never (UKB data field 22607_0) 96,088 European ancestry cases, 17,199 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043266 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very cold: PHESANT recoding (UKB data field 22607_1) 53,726 European ancestry cases, 59,318 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043267 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very cold: PHESANT recoding (UKB data field 22607_2) 9,976 European ancestry cases, 102,659 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043268 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very hot: Rarely/never (UKB data field 22608_0) 85,715 European ancestry cases, 27,505 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043269 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very hot: PHESANT recoding (UKB data field 22608_1) 65,353 European ancestry cases, 47,726 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043270 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very hot: PHESANT recoding (UKB data field 22608_2) 12,839 European ancestry cases, 99,741 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043271 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very dusty: Rarely/never (UKB data field 22609_0) 101,558 European ancestry cases, 11,508 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043272 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very dusty: PHESANT recoding (UKB data field 22609_1) 39,647 European ancestry cases, 72,705 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043273 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace very dusty: PHESANT recoding (UKB data field 22609_2) 12,167 European ancestry cases, 99,743 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043274 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace full of chemical or other fumes: Rarely/never (UKB data field 22610_0) 106,600 European ancestry cases, 6,211 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043275 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: travel/tour guide (UKB data field 22601_62133370) 237 European ancestry cases, 112,041 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043176 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: air travel assistant, cabin/flight attendant, air hostess, air purser, air steward, cabin crew; passenger services agent; check-in staff (UKB data field 22601_62142638) 297 European ancestry cases, 111,981 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043177 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: air hostess, air steward, air travel assistant, cabin/flight attendant, cabin crew, air purser, passenger services agent, check-in-staff (UKB data field 22601_62143372) 154 European ancestry cases, 112,124 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043178 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: bus conductor (UKB data field 22601_62192607) 158 European ancestry cases, 112,120 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043179 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: hairdresser, barber, shampooist, hair stylist (UKB data field 22601_62213359) 523 European ancestry cases, 111,755 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043180 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: housekeeper, butler, valet, cook-housekeeper, companion-housekeeper (UKB data field 22601_62312996) 426 European ancestry cases, 111,852 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043181 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: caretaker, janitor, concierge, warden (UKB data field 22601_62322997) 170 European ancestry cases, 112,108 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043182 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: school/college caretaker/porter (UKB data field 22601_62323000) 127 European ancestry cases, 112,151 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043183 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sales assistant, retail/shop assistant, counter assistant, sub post office assistant, takeaway food worker (UKB data field 22601_71113328) 5,804 European ancestry cases, 106,474 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043184 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: retail/shop cashier, check-out operator, petrol station attendant, restaurant cashier (UKB data field 22601_71123329) 1,066 European ancestry cases, 111,212 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043185 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: collector/door-to-door salesperson, canvasser, credit agent, insurance agent, travelling salesperson, commercial traveller (UKB data field 22601_71213337) 1,004 European ancestry cases, 111,274 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043186 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: roundsman or woman, van salesperson, ice cream seller, milkman, mobile shop salesperson (UKB data field 22601_71233339) 325 European ancestry cases, 111,953 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043187 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: market or street trader/assistant, stall holder, newspaper seller (UKB data field 22601_71243340) 125 European ancestry cases, 112,153 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043188 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: merchandiser, window dresser (UKB data field 22601_71253330) 242 European ancestry cases, 112,036 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043189 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: advertising or sales representative, demonstrator, estate agent negotiator, land/property salesman (UKB data field 22601_71293332) 278 European ancestry cases, 112,000 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043190 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other sales-related work including car hirer, skip hire operator, rental operator, sales promoter, film/video renter, money lender (UKB data field 22601_71293335) 120 European ancestry cases, 112,158 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043191 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: advertising or sales representative, demonstrator, estate agent negotiator, land/property salesman (UKB data field 22601_71293343) 930 European ancestry cases, 111,348 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043192 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: call centre operator, sales order clerk, telephone adviser (UKB data field 22601_72113242) 904 European ancestry cases, 111,374 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043193 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: customer care adviser/officer/assistant, store guide, customer relations officer/representative (UKB data field 22601_72123243) 1,533 European ancestry cases, 110,745 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043194 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: customer care adviser/officer/assistant, store guide, customer relations officer/representative (UKB data field 22601_72123325) 608 European ancestry cases, 111,670 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043195 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: machine operator, processor, foreman (UKB data field 22601_81112700) 294 European ancestry cases, 111,984 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043196 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: textile machine operator, assembler, spinner, foreman (UKB data field 22601_81132710) 327 European ancestry cases, 111,951 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043197 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: machine operator, processor, paint maker, foreman (UKB data field 22601_81142763) 132 European ancestry cases, 112,146 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043198 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: machine operator, plastics moulder, foreman (UKB data field 22601_81162743) 227 European ancestry cases, 112,051 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043199 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: metal making or metal treating process worker, machine operator, furnaceman (UKB data field 22601_81172834) 152 European ancestry cases, 112,126 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043200 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: driving instructor, hgv instructor (UKB data field 22601_82152612) 156 European ancestry cases, 112,122 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043226 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: merchant seaman, seafarer, deckhand, boatman (UKB data field 22601_82172651) 101 European ancestry cases, 112,177 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043227 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: farmhand, farm labourer, herdsman, shepherd, dairyman, pigman (UKB data field 22601_91112478) 458 European ancestry cases, 111,820 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043228 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: nursery worker/hand, horticultural worker, fruit picker, mushroom picker and other pickers (UKB data field 22601_91192487) 161 European ancestry cases, 112,117 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043229 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: builder's labourer, building worker, hod carrier (UKB data field 22601_91212536) 474 European ancestry cases, 111,804 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043230 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: builder's labourer, building worker (UKB data field 22601_91212550) 152 European ancestry cases, 112,126 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043231 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: factory cleaner/industrial cleaner in some other setting (UKB data field 22601_91322983) 130 European ancestry cases, 112,148 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043232 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: printing machine operator, printer's assistant (UKB data field 22601_91332890) 151 European ancestry cases, 112,127 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043233 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: packer, bottler, canner, filler, wrapper, foreman (UKB data field 22601_91342701) 327 European ancestry cases, 111,951 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043234 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other work in this industry: factory hand, mate, assistant, handler, loader (UKB data field 22601_91392708) 114 European ancestry cases, 112,164 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043235 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other work in this industry: factory hand, mate, assistant, handler, loader, finisher (UKB data field 22601_91392721) 146 European ancestry cases, 112,132 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043236 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other work in this industry: factory hand, mate, assistant, handler, loader (UKB data field 22601_91392782) 124 European ancestry cases, 112,154 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043237 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other work in this industry: factory hand, mate, assistant, handler, loader (UKB data field 22601_91392832) 172 European ancestry cases, 112,106 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043238 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other work in these industries: attendant, hand, mate, assistant, handler, loader (UKB data field 22601_91392859) 133 European ancestry cases, 112,145 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043239 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sales room assistant, wine merchant's cellar man; order/stock filler, stock/store keeper; lorry/warehouse loader/checker/weigher, goods porter, customs attendant (UKB data field 22601_91493353) 253 European ancestry cases, 112,025 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043240 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: stores/warehouse porter (UKB data field 22601_91493354) 178 European ancestry cases, 112,100 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043241 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other work handling or storing goods including: store keeper, warehouseman, order assembler, goods despatcher (UKB data field 22601_91493355) 738 European ancestry cases, 111,540 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043242 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: postal worker, postman, mail sorter, messenger, courier, mailroom clerk, post sorter, leaflet/circular distributor, newspaper/parcel deliverer (UKB data field 22601_92113311) 491 European ancestry cases, 111,787 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043243 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: postal worker, postman, mail sorter, messenger, courier, mailroom clerk, post sorter, leaflet/circular distributor, newspaper/parcel deliverer (UKB data field 22601_92113352) 338 European ancestry cases, 111,940 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043244 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other general office clerical tasks including: office junior, office worker, photocopy/print room operator, office machinist (UKB data field 22601_92193312) 4,196 European ancestry cases, 108,082 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043245 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: hotel and other accommodation porter, bell hop (UKB data field 22601_92223394) 102 European ancestry cases, 112,176 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043246 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: kitchen, canteen or catering assistant, washer-up, kitchen porter, counter assistant (UKB data field 22601_92233387) 450 European ancestry cases, 111,828 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043247 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: dinner lady (UKB data field 22601_92233412) 208 European ancestry cases, 62,377 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043248 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: waiter, waitress, maitre d'hotel, sommelier, steward (UKB data field 22601_92243389) 672 European ancestry cases, 111,606 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043249 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: bar staff, cellarman (public house) (UKB data field 22601_92253391) 787 European ancestry cases, 111,491 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043250 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: builder, building contractor (UKB data field 22601_53192549) 152 European ancestry cases, 112,126 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043151 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: painter, decorator (UKB data field 22601_53232556) 397 European ancestry cases, 111,881 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043152 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: weaver, knitter, carpet weaver, net maker (UKB data field 22601_54112877) 111 European ancestry cases, 112,167 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043153 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: upholsterer, coach trimmer, curtain maker, mattress maker (UKB data field 22601_54122878) 124 European ancestry cases, 112,154 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043154 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: tailor, dressmaker, milliner (UKB data field 22601_54142880) 212 European ancestry cases, 112,066 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043155 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: compositor, originator, lithographic plate maker, paste-up artist, stereotyper, typesetter (UKB data field 22601_54212886) 230 European ancestry cases, 112,048 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043156 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: printer, master printer (UKB data field 22601_54222887) 143 European ancestry cases, 112,135 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043157 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: bookbinder, print finisher, collator, binder's assistant, darkroom technician (UKB data field 22601_54232888) 110 European ancestry cases, 112,168 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043158 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: butcher, meat cutter, slaughterer (UKB data field 22601_54312892) 104 European ancestry cases, 112,174 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043159 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: baker, confectioner, pastry cook, cake decorator (UKB data field 22601_54322893) 207 European ancestry cases, 112,071 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043160 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chef, cook, caterer (UKB data field 22601_54342896) 430 European ancestry cases, 111,848 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043161 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chef, cook, caterer (UKB data field 22601_54343385) 603 European ancestry cases, 111,675 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043162 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: furniture maker/fitter, cabinet maker (UKB data field 22601_54922904) 198 European ancestry cases, 112,080 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043163 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: nursing auxiliary or assistant, steriliser of medical equipment, occupational therapy assistant, phlebotomist, physiotherapy assistant, ward orderly, ward assistant (UKB data field 22601_61113073) 1,594 European ancestry cases, 110,684 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043164 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: dental nurse or assistant (UKB data field 22601_61133076) 283 European ancestry cases, 111,995 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043165 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: houseparent, child careworker, residential warden, sheltered accommodation warden, foster parent (UKB data field 22601_61143103) 826 European ancestry cases, 111,452 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043166 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: care assistant, home care assistant, residential social worker, home carer, nursing home assistant (UKB data field 22601_61153104) 1,525 European ancestry cases, 110,753 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043167 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: nursery nurse/assistant/supervisor, creche assistant (UKB data field 22601_61213416) 411 European ancestry cases, 111,867 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043168 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: childminder, au pair, children's nanny (UKB data field 22601_61223105) 620 European ancestry cases, 111,658 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043169 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: childminder, au pair, children's nanny (UKB data field 22601_61223417) 527 European ancestry cases, 111,751 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043170 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: playgroup or playschool leader or assistant (UKB data field 22601_61233408) 574 European ancestry cases, 111,704 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043171 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: educational assistant, classroom assistant, special needs helper (UKB data field 22601_61243409) 2,824 European ancestry cases, 109,454 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043172 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other animal care work including dog beautician, dog walker, dog warden; kennel or cattery assistant; groom, huntsman, stable worker; zoo keeper (UKB data field 22601_61392517) 186 European ancestry cases, 112,092 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043173 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sports assistant, lifeguard, swimming pool attendant, gym attendant, bowling green attendant (UKB data field 22601_62113142) 105 European ancestry cases, 112,173 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043174 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: travel agent, travel agency/booking/reservations clerk, tour organiser (UKB data field 22601_62123369) 510 European ancestry cases, 111,768 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043175 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: machine operator, processor, foreman (UKB data field 22601_81212774) 203 European ancestry cases, 112,075 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043201 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: coal worker or miner (surface or underground) (UKB data field 22601_81222848) 327 European ancestry cases, 111,951 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043202 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: energy plant operator, stoker, boiler operator, substation or power station attendant (UKB data field 22601_81242853) 122 European ancestry cases, 49,571 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043203 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: metal working machine operator, fettler, grinder, metal cutter, metal machinist, metal polisher, press operator, shot blaster, tool room machinist (UKB data field 22601_81252835) 168 European ancestry cases, 112,110 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043204 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: assembler, machine operator, foreman (UKB data field 22601_81312794) 408 European ancestry cases, 111,870 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043205 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: wireman, coil winder, wirer (UKB data field 22601_81312795) 130 European ancestry cases, 112,148 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043206 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: assembler, machine operator, foreman (UKB data field 22601_81322804) 406 European ancestry cases, 111,872 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043207 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: assembler, machine operator, foreman (UKB data field 22601_81322815) 269 European ancestry cases, 112,009 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043208 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: routine inspector, tester (UKB data field 22601_81332797) 120 European ancestry cases, 112,158 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043209 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sewing machinist (UKB data field 22601_81372713) 589 European ancestry cases, 111,689 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043210 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392707) 128 European ancestry cases, 112,150 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043211 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392720) 114 European ancestry cases, 112,164 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043212 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392750) 116 European ancestry cases, 112,162 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043213 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392781) 131 European ancestry cases, 112,147 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043214 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392801) 191 European ancestry cases, 112,087 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043215 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392812) 145 European ancestry cases, 112,133 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043216 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392821) 129 European ancestry cases, 112,149 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043217 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: assembler, machine operator, processor, foreman (UKB data field 22601_81392824) 306 European ancestry cases, 111,972 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043218 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other assembler, routine operative (UKB data field 22601_81392831) 208 European ancestry cases, 112,070 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043219 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: building site foreman or supervisor (UKB data field 22601_81492535) 236 European ancestry cases, 112,042 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043220 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: building site foreman or supervisor (UKB data field 22601_81492548) 145 European ancestry cases, 112,133 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043221 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: heavy goods vehicle (hgv) driver, lorry or truck driver, tanker driver, haulage driver (UKB data field 22601_82112603) 826 European ancestry cases, 111,452 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043222 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: van driver, delivery driver, courier driver (UKB data field 22601_82122605) 984 European ancestry cases, 111,294 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043223 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: bus or coach driver, minibus driver (UKB data field 22601_82132606) 509 European ancestry cases, 111,769 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043224 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: taxi or cab driver, chauffeur, hearse driver (UKB data field 22601_82142611) 310 European ancestry cases, 111,968 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043225 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cardiac arrest (PheCode 427.42) 244 European ancestry cases, 456,104 European ancestry controls NA NR [11842647] (imputed) 0 GCST90043979 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Arrhythmia (cardiac), not otherwise specified (PheCode 427.5) 355 European ancestry cases, 455,993 European ancestry controls NA NR [11842647] (imputed) 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90043980 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Premature beats (PheCode 427.6) 218 European ancestry cases, 456,130 European ancestry controls NA NR [11842647] (imputed) 0 premature cardiac contractions http://www.ebi.ac.uk/efo/EFO_0009275 GCST90043981 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tachycardia, not otherwise specified (PheCode 427.7) 292 European ancestry cases, 456,056 European ancestry controls NA NR [11842647] (imputed) 0 Tachycardia http://purl.obolibrary.org/obo/HP_0001649 GCST90043982 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sinoatrial node dysfunction (Bradycardia) (PheCode 427.8) 272 European ancestry cases, 456,076 European ancestry controls NA NR [11842647] (imputed) 0 Bradycardia http://purl.obolibrary.org/obo/HP_0001662 GCST90043983 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Palpitations (PheCode 427.9) 2,311 European ancestry cases, 454,037 European ancestry controls NA NR [11842647] (imputed) 0 Palpitations http://purl.obolibrary.org/obo/HP_0001962 GCST90043984 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congestive heart failure (CHF), not otherwise specified (PheCode 428.1) 897 European ancestry cases, 455,451 European ancestry controls NA NR [11842647] (imputed) 0 congestive heart failure http://www.ebi.ac.uk/efo/EFO_0000373 GCST90043985 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Heart failure, not otherwise specified (PheCode 428.2) 1,029 European ancestry cases, 455,319 European ancestry controls NA NR [11842647] (imputed) 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90043986 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal function study of cardiovascular system (PheCode 429.2) 113 European ancestry cases, 456,235 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal cardiovascular system physiology http://purl.obolibrary.org/obo/HP_0011025 GCST90043987 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms involving cardiovascular system (PheCode 429.3) 117 European ancestry cases, 456,231 European ancestry controls NA NR [11842647] (imputed) 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90043988 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prospective memory test: number of attempts (UKB data field 4291) 30,866 European ancestry cases, 119,299 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90043989 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prospective memory test: final attempt correct: no (UKB data field 4294_0) 6,024 European ancestry cases, 144,141 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90043990 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prospective memory test: final attempt correct: yes (UKB data field 4294_1) 143,956 European ancestry cases, 6,209 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90043991 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prospective memory test: final attempt correct: abandon (UKB data field 4294_9) 185 European ancestry cases, 149,980 European ancestry controls NA NR [11842647] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90043992 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Subarachnoid hemorrhage (PheCode 430.1) 832 European ancestry cases, 455,516 European ancestry controls NA NR [11842647] (imputed) 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90043993 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Intracerebral hemorrhage (PheCode 430.2) 655 European ancestry cases, 455,693 European ancestry controls NA NR [11842647] (imputed) 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90043994 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Subdural hemorrhage (PheCode 430.3) 244 European ancestry cases, 456,104 European ancestry controls NA NR [11842647] (imputed) 0 Subdural hemorrhage http://purl.obolibrary.org/obo/HP_0100309 GCST90043995 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Intracranial hemorrhage (PheCode 430) 158 European ancestry cases, 456,190 European ancestry controls NA NR [11842647] (imputed) 0 intracranial hemorrhage http://www.ebi.ac.uk/efo/EFO_0000551 GCST90043996 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Occlusion of cerebral arteries, with cerebral infarction (PheCode 433.11) 134 European ancestry cases, 456,214 European ancestry controls NA NR [11842647] (imputed) 0 stroke, occlusion precerebral artery http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0009677 GCST90043997 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Occlusion and stenosis of precerebral arteries (PheCode 433.1) 630 European ancestry cases, 455,718 European ancestry controls NA NR [11842647] (imputed) 0 occlusion precerebral artery http://www.ebi.ac.uk/efo/EFO_0009677 GCST90043998 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cerebral artery occlusion, with cerebral infarction (PheCode 433.21) 1,830 European ancestry cases, 454,518 European ancestry controls NA NR [11842647] (imputed) 0 stroke, occlusion precerebral artery http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0009677 GCST90043999 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Occlusion of cerebral arteries (PheCode 433.2) 2,968 European ancestry cases, 453,380 European ancestry controls NA NR [11842647] (imputed) 0 brain infarction http://www.ebi.ac.uk/efo/EFO_0004277 GCST90044000 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Transient cerebral ischemia (PheCode 433.31) 2,045 European ancestry cases, 454,303 European ancestry controls NA NR [11842647] (imputed) 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90044001 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cerebral ischemia (PheCode 433.3) 106 European ancestry cases, 456,242 European ancestry controls NA NR [11842647] (imputed) 0 Cerebral ischemia http://purl.obolibrary.org/obo/HP_0002637 GCST90044002 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cerebral aneurysm (PheCode 433.5) 290 European ancestry cases, 456,058 European ancestry controls NA NR [11842647] (imputed) 0 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90044003 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cerebrovascular disease (PheCode 433) 475 European ancestry cases, 455,873 European ancestry controls NA NR [11842647] (imputed) 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90044004 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Atherosclerosis of the extremities (PheCode 440.2) 635 European ancestry cases, 455,713 European ancestry controls NA NR [11842647] (imputed) 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90044005 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Atherosclerosis (PheCode 440) 106 European ancestry cases, 456,242 European ancestry controls NA NR [11842647] (imputed) 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90044006 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute vascular insufficiency of intestine (PheCode 441.1) 143 European ancestry cases, 456,205 European ancestry controls NA NR [11842647] (imputed) 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90044007 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vascular insufficiency of intestine (PheCode 441) 164 European ancestry cases, 456,184 European ancestry controls NA NR [11842647] (imputed) 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90044008 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abdominal aortic aneurysm (PheCode 442.11) 556 European ancestry cases, 455,792 European ancestry controls NA NR [11842647] (imputed) 0 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST90044009 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aortic aneurysm (PheCode 442.1) 258 European ancestry cases, 456,090 European ancestry controls NA NR [11842647] (imputed) 0 aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0001666 GCST90044010 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aneurysm of artery of lower extremity (PheCode 442.3) 123 European ancestry cases, 456,225 European ancestry controls NA NR [11842647] (imputed) 0 aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0001666 GCST90044011 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aneurysm of other specified artery (PheCode 442.8) 124 European ancestry cases, 456,224 European ancestry controls NA NR [11842647] (imputed) 0 aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0001666 GCST90044012 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Raynaud's syndrome (PheCode 443.1) 111 European ancestry cases, 456,237 European ancestry controls NA NR [11842647] (imputed) 0 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90044013 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peripheral angiopathy in diseases classified elsewhere (PheCode 443.7) 227 European ancestry cases, 456,121 European ancestry controls NA NR [11842647] (imputed) 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90044014 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peripheral vascular disease, unspecified (PheCode 443.9) 847 European ancestry cases, 455,501 European ancestry controls NA NR [11842647] (imputed) 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90044015 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Arterial embolism and thrombosis of lower extremity artery (PheCode 444.1) 454 European ancestry cases, 455,894 European ancestry controls NA NR [11842647] (imputed) 0 arterial embolism http://www.ebi.ac.uk/efo/EFO_0010671 GCST90044016 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Arterial embolism and thrombosis (PheCode 444) 303 European ancestry cases, 456,045 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044017 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Wegener's granulomatosis (PheCode 446.4) 135 European ancestry cases, 456,213 European ancestry controls NA NR [11842647] (imputed) 0 Granulomatosis with Polyangiitis http://www.ebi.ac.uk/efo/EFO_0005297 GCST90044018 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Giant cell arteritis (PheCode 446.5) 278 European ancestry cases, 456,070 European ancestry controls NA NR [11842647] (imputed) 0 temporal arteritis http://www.ebi.ac.uk/efo/EFO_1001209 GCST90044019 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Arteritis, not otherwise specified (PheCode 446.9) 113 European ancestry cases, 456,235 European ancestry controls NA NR [11842647] (imputed) 0 Arteritis http://www.ebi.ac.uk/efo/EFO_0009011 GCST90044020 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Stricture of artery (PheCode 447.1) 639 European ancestry cases, 455,709 European ancestry controls NA NR [11842647] (imputed) 0 stricture http://www.ebi.ac.uk/efo/EFO_0006818 GCST90044021 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of arteries and arterioles (PheCode 447) 353 European ancestry cases, 455,995 European ancestry controls NA NR [11842647] (imputed) 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90044022 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-accidental death in close genetic family (UKB data field 4501) 38,904 European ancestry cases, 103,594 European ancestry controls NA NR [11842647] (imputed) 0 event death, family history http://www.ebi.ac.uk/efo/EFO_0000480, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90044023 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Noninfectious disorders of lymphatic channels (PheCode 450) 203 European ancestry cases, 456,145 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044024 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Phlebitis and thrombophlebitis of lower extremities (PheCode 451.2) 2,996 European ancestry cases, 453,352 European ancestry controls NA NR [11842647] (imputed) 1 Phlebitis http://www.ebi.ac.uk/efo/EFO_1001395 GCST90044025 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Phlebitis and thrombophlebitis (PheCode 451) 195 European ancestry cases, 456,153 European ancestry controls NA NR [11842647] (imputed) 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90044026 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other venous embolism and thrombosis (PheCode 452) 241 European ancestry cases, 456,107 European ancestry controls NA NR [11842647] (imputed) 0 Portal vein thrombosis http://purl.obolibrary.org/obo/HP_0030242 GCST90044027 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Varicose veins of lower extremity, symptomtic (PheCode 454.11) 498 European ancestry cases, 455,850 European ancestry controls NA NR [11842647] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90044028 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Varicose veins of lower extremity (PheCode 454.1) 11,000 European ancestry cases, 445,348 European ancestry controls NA NR [11842647] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90044029 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Varicose veins (PheCode 454) 299 European ancestry cases, 456,049 European ancestry controls NA NR [11842647] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90044030 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemorrhoids (PheCode 455) 16,179 European ancestry cases, 440,169 European ancestry controls NA NR [11842647] (imputed) 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90044031 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Orthostatic hypotension (PheCode 458.1) 574 European ancestry cases, 455,774 European ancestry controls NA NR [11842647] (imputed) 0 orthostatic hypotension http://www.ebi.ac.uk/efo/EFO_0005252 GCST90044032 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Iatrogenic hypotension (PheCode 458.2) 112 European ancestry cases, 456,236 European ancestry controls NA NR [11842647] (imputed) 0 hypotension http://www.ebi.ac.uk/efo/EFO_0005251 GCST90044033 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypotension, not otherwise specified (PheCode 458.9) 251 European ancestry cases, 456,097 European ancestry controls NA NR [11842647] (imputed) 0 hypotension http://www.ebi.ac.uk/efo/EFO_0005251 GCST90044034 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Circulatory disease NEC (PheCode 459.9) 184 European ancestry cases, 456,164 European ancestry controls NA NR [11842647] (imputed) 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90044035 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever depressed for a whole week (UKB data field 4598) 79,315 European ancestry cases, 68,230 European ancestry controls NA NR [11842647] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90044036 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever unenthusiastic/disinterested for a whole week (UKB data field 4631) 53,353 European ancestry cases, 90,951 European ancestry controls NA NR [11842647] (imputed) 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90044037 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever manic hyper for 2 days (UKB data field 4642) 8,449 European ancestry cases, 138,388 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044038 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute sinusitis (PheCode 464) 161 European ancestry cases, 456,187 European ancestry controls NA NR [11842647] (imputed) 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90044039 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute pharyngitis (PheCode 465.2) 459 European ancestry cases, 455,889 European ancestry controls NA NR [11842647] (imputed) 0 acute pharyngitis http://www.ebi.ac.uk/efo/EFO_0009657 GCST90044040 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute laryngitis and tracheitis (PheCode 465.4) 117 European ancestry cases, 456,231 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044041 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever highly irritable - argumentative for 2 days (UKB data field 4653) 26,667 European ancestry cases, 120,501 European ancestry controls NA NR [11842647] (imputed) 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90044042 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute upper respiratory infections of multiple or unspecified sites (PheCode 465) 667 European ancestry cases, 455,681 European ancestry controls NA NR [11842647] (imputed) 0 common cold http://www.ebi.ac.uk/efo/EFO_0007214 GCST90044043 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Septal Deviations/Turbinate Hypertrophy (PheCode 470) 4,112 European ancestry cases, 452,236 European ancestry controls NA NR [11842647] (imputed) 0 hypertrophy http://www.ebi.ac.uk/efo/EFO_0002460 GCST90044044 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Shortness of breath walking on level ground (UKB data field 4717) 15,781 European ancestry cases, 132,174 European ancestry controls NA NR [11842647] (imputed) 0 shortness of breath http://www.ebi.ac.uk/efo/EFO_0009727 GCST90044045 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nasal polyps (PheCode 471) 2,863 European ancestry cases, 453,485 European ancestry controls NA NR [11842647] (imputed) 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90044046 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic pharyngitis and nasopharyngitis (PheCode 472) 393 European ancestry cases, 455,955 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044047 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Paralysis/spasm of vocal cords or larynx (PheCode 473.3) 143 European ancestry cases, 456,205 European ancestry controls NA NR [11842647] (imputed) 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90044048 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Voice disturbance (PheCode 473.4) 743 European ancestry cases, 455,605 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044049 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of the larynx and vocal cords (PheCode 473) 1,470 European ancestry cases, 454,878 European ancestry controls NA NR [11842647] (imputed) 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90044050 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute tonsillitis (PheCode 474.1) 548 European ancestry cases, 455,800 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044051 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic tonsillitis and adenoiditis (PheCode 474.2) 939 European ancestry cases, 455,409 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044052 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute and chronic tonsillitis (PheCode 474) 449 European ancestry cases, 455,899 European ancestry controls NA NR [11842647] (imputed) 0 peritonsillar abscess http://www.ebi.ac.uk/efo/EFO_0007429 GCST90044053 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Angina pectoris (PheCode 411.3) 5,786 European ancestry cases, 450,562 European ancestry controls NA NR [11842647] (imputed) 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90043955 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aneurysm and dissection of heart (PheCode 411.41) 234 European ancestry cases, 456,114 European ancestry controls NA NR [11842647] (imputed) 0 heart aneurysm http://www.ebi.ac.uk/efo/EFO_1000959 GCST90043956 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Coronary atherosclerosis (PheCode 411.4) 16,041 European ancestry cases, 440,307 European ancestry controls NA NR [11842647] (imputed) 1 coronary atherosclerosis http://purl.obolibrary.org/obo/MONDO_0021661 GCST90043957 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other chronic ischemic heart disease, unspecified (PheCode 411.8) 2,074 European ancestry cases, 454,274 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043958 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other acute and subacute forms of ischemic heart disease (PheCode 411.9) 575 European ancestry cases, 455,773 European ancestry controls NA NR [11842647] (imputed) 0 Myocardial Ischemia http://www.ebi.ac.uk/efo/EFO_1001375 GCST90043959 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other forms of chronic heart disease (PheCode 414) 177 European ancestry cases, 456,171 European ancestry controls NA NR [11842647] (imputed) 0 Myocardial Ischemia http://www.ebi.ac.uk/efo/EFO_1001375 GCST90043960 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Primary pulmonary hypertension (PheCode 415.21) 99 European ancestry cases, 456,249 European ancestry controls NA NR [11842647] (imputed) 0 primary pulmonary hypertension http://purl.obolibrary.org/obo/MONDO_0001999 GCST90043961 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pulmonary heart disease (PheCode 415) 2,971 European ancestry cases, 453,377 European ancestry controls NA NR [11842647] (imputed) 0 cor pulmonale http://purl.obolibrary.org/obo/MONDO_0004596 GCST90043962 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cardiomegaly (PheCode 416) 115 European ancestry cases, 456,233 European ancestry controls NA NR [11842647] (imputed) 0 cardiac hypertrophy http://www.ebi.ac.uk/efo/EFO_0002503 GCST90043963 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Precordial pain (PheCode 418.1) 3,659 European ancestry cases, 452,689 European ancestry controls NA NR [11842647] (imputed) 0 Precordial pain http://purl.obolibrary.org/obo/HP_0032141 GCST90043964 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nonspecific chest pain (PheCode 418) 29,202 European ancestry cases, 427,146 European ancestry controls NA NR [11842647] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90043965 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute pericarditis (PheCode 420.21) 187 European ancestry cases, 456,161 European ancestry controls NA NR [11842647] (imputed) 0 pericarditis http://www.ebi.ac.uk/efo/EFO_0007427 GCST90043966 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pericarditis (PheCode 420.2) 526 European ancestry cases, 455,822 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043967 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Endocarditis (PheCode 420.3) 267 European ancestry cases, 456,081 European ancestry controls NA NR [11842647] (imputed) 0 endocarditis http://www.ebi.ac.uk/efo/EFO_0000465 GCST90043968 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Primary/intrinsic cardiomyopathies (PheCode 425.1) 522 European ancestry cases, 455,826 European ancestry controls NA NR [11842647] (imputed) 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST90043969 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. First degree AV block (PheCode 426.21) 162 European ancestry cases, 456,186 European ancestry controls NA NR [11842647] (imputed) 0 First degree atrioventricular block http://purl.obolibrary.org/obo/HP_0011705 GCST90043970 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Second degree AV block (PheCode 426.23) 215 European ancestry cases, 456,133 European ancestry controls NA NR [11842647] (imputed) 0 Second degree atrioventricular block http://purl.obolibrary.org/obo/HP_0011706 GCST90043971 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Atrioventricular block, complete (PheCode 426.24) 369 European ancestry cases, 455,979 European ancestry controls NA NR [11842647] (imputed) 0 third-degree atrioventricular block http://purl.obolibrary.org/obo/MONDO_0000468 GCST90043972 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Left bundle branch block (PheCode 426.32) 170 European ancestry cases, 456,178 European ancestry controls NA NR [11842647] (imputed) 0 Left bundle branch block http://purl.obolibrary.org/obo/HP_0011713 GCST90043973 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anomalous atrioventricular excitation (PheCode 426.4) 123 European ancestry cases, 456,225 European ancestry controls NA NR [11842647] (imputed) 0 conduction system disorder http://www.ebi.ac.uk/efo/EFO_0005137 GCST90043974 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Paroxysmal supraventricular tachycardia (PheCode 427.11) 1,728 European ancestry cases, 454,620 European ancestry controls NA NR [11842647] (imputed) 0 Paroxysmal supraventricular tachycardia http://purl.obolibrary.org/obo/HP_0004763 GCST90043975 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Paroxysmal ventricular tachycardia (PheCode 427.12) 580 European ancestry cases, 455,768 European ancestry controls NA NR [11842647] (imputed) 0 Paroxysmal ventricular tachycardia http://purl.obolibrary.org/obo/HP_0004751 GCST90043976 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Atrial fibrillation and flutter (PheCode 427.2) 8,404 European ancestry cases, 447,944 European ancestry controls NA NR [11842647] (imputed) 2 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90043977 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other specified cardiac dysrhythmias (PheCode 427.3) 899 European ancestry cases, 455,449 European ancestry controls NA NR [11842647] (imputed) 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90043978 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Myocardial infarction (PheCode 411.2) 8,528 European ancestry cases, 447,820 European ancestry controls NA NR [11842647] (imputed) 1 acute myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008583 GCST90043954 Genome-wide genotyping array 2022-04-01 34899825 Jiao H 2021-11-25 Front Genet www.ncbi.nlm.nih.gov/pubmed/34899825 Pathway Association Studies Reveal Gene Loci and Pathway Networks that Associated With Plasma Cystatin C Levels. Cystatin C plasma levels 460,858 European or unknown ancestry individuals NA Affymetrix [NR] (imputed) 25 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90100559 Genome-wide genotyping array 2022-04-01 34899825 Jiao H 2021-11-25 Front Genet www.ncbi.nlm.nih.gov/pubmed/34899825 Pathway Association Studies Reveal Gene Loci and Pathway Networks that Associated With Plasma Cystatin C Levels. Creatinine levels up to 460,858 European or unknown ancestry individuals NA Affymetrix [NR] (imputed) 7 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90100560 Genome-wide genotyping array 2022-04-01 34899825 Jiao H 2021-11-25 Front Genet www.ncbi.nlm.nih.gov/pubmed/34899825 Pathway Association Studies Reveal Gene Loci and Pathway Networks that Associated With Plasma Cystatin C Levels. Estimated glomerular filtration rate up to 460,858 European or unknown ancestry individuals NA Affymetrix [NR] (imputed) 5 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90100561 Genome-wide genotyping array 2022-04-01 34899825 Jiao H 2021-11-25 Front Genet www.ncbi.nlm.nih.gov/pubmed/34899825 Pathway Association Studies Reveal Gene Loci and Pathway Networks that Associated With Plasma Cystatin C Levels. Urea levels up to 460,858 European or unknown ancestry individuals NA Affymetrix [NR] (imputed) 6 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90100562 Genome-wide genotyping array 2022-01-18 34707639 Liu T 2021-10-11 Front Genet www.ncbi.nlm.nih.gov/pubmed/34707639 Exome-Wide Association Study Identifies East Asian-Specific Missense Variant MTHFR C136T Influencing Homocysteine Levels in Chinese Populations RH: ExWAS of tHCY in a Chinese Population. Homocysteine levels 5,175 Han Chinese ancestry individuals 688 Han Chinese ancestry individuals Illumina [89131] 1 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST90090974 Exome genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mirena 20mcg/24hrs intrauterine system (UKB data field 20003_1140921822) 701 European ancestry cases, 246,807 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042326 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dicloflex 25mg e/c tablet (UKB data field 20003_1140921828) 544 European ancestry cases, 455,732 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042327 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - alendronate sodium (UKB data field 20003_1140922174) 5,255 European ancestry cases, 451,021 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042328 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - femoston 1/10 tablet (UKB data field 20003_1140922562) 721 European ancestry cases, 246,787 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042329 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dorzolamide (UKB data field 20003_1140922714) 113 European ancestry cases, 456,163 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042330 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - premique 0.625mg/5mg tablet (UKB data field 20003_1140922804) 887 European ancestry cases, 246,621 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042331 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - premique cycle 10mg tablet (UKB data field 20003_1140922806) 157 European ancestry cases, 247,351 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042332 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - anastrozole (UKB data field 20003_1140923018) 412 European ancestry cases, 247,096 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042333 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - arimidex 1mg tablet (UKB data field 20003_1140923022) 799 European ancestry cases, 455,477 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042334 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-amilozide (UKB data field 20003_1140923276) 257 European ancestry cases, 456,019 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042335 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-tenidone (UKB data field 20003_1140923336) 653 European ancestry cases, 455,623 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042336 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-codamol (UKB data field 20003_1140923346) 10,689 European ancestry cases, 445,587 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042337 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-proxamol (UKB data field 20003_1140923348) 367 European ancestry cases, 455,909 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042338 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-dydramol (UKB data field 20003_1140923350) 2,868 European ancestry cases, 453,408 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042339 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-amilofruse (UKB data field 20003_1140923402) 443 European ancestry cases, 455,833 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042340 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - topiramate (UKB data field 20003_1140923484) 246 European ancestry cases, 456,030 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042341 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - adipine mr 10 m/r tablet (UKB data field 20003_1140923572) 160 European ancestry cases, 456,116 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042342 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - gtn - glyceryl trinitrate (UKB data field 20003_1140923670) 782 European ancestry cases, 455,494 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042343 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zoton 15mg capsule (UKB data field 20003_1140923688) 316 European ancestry cases, 455,960 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042344 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - femseven 50 patch (UKB data field 20003_1140923738) 186 European ancestry cases, 456,090 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042345 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - elleste-solo 1mg tablet (UKB data field 20003_1140923852) 786 European ancestry cases, 246,722 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042346 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - movicol oral powder (UKB data field 20003_1140925800) 1,424 European ancestry cases, 454,852 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042347 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mycophenolate (UKB data field 20003_1140925978) 198 European ancestry cases, 456,078 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042348 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - climesse tablet (UKB data field 20003_1140926430) 179 European ancestry cases, 247,329 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042349 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - estraderm mx 25 patch (UKB data field 20003_1140926592) 711 European ancestry cases, 246,797 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042350 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - insulin product (UKB data field 20003_1140883066) 4,469 European ancestry cases, 451,807 European ancestry controls NA NR [11842647] (imputed) 2 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042226 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clonidine (UKB data field 20003_1140883468) 587 European ancestry cases, 455,689 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042227 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cetirizine (UKB data field 20003_1140883504) 5,135 European ancestry cases, 451,141 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042228 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - chlorpheniramine (UKB data field 20003_1140883520) 114 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042229 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cinnarizine (UKB data field 20003_1140883524) 235 European ancestry cases, 456,041 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042230 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ipratropium (UKB data field 20003_1140883548) 563 European ancestry cases, 455,713 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042231 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oxybutynin (UKB data field 20003_1140883568) 1,034 European ancestry cases, 455,242 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042232 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hydroxyzine (UKB data field 20003_1140883656) 139 European ancestry cases, 456,137 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042233 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pizotifen (UKB data field 20003_1140883664) 685 European ancestry cases, 455,591 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042234 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - selenium product (UKB data field 20003_1140883748) 1,383 European ancestry cases, 454,893 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042235 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - carmellose (UKB data field 20003_1140883968) 178 European ancestry cases, 456,098 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042236 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hydroxychloroquine (UKB data field 20003_1140884308) 627 European ancestry cases, 455,649 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042237 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sumatriptan (UKB data field 20003_1140884412) 1,226 European ancestry cases, 455,050 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042238 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - codeine (UKB data field 20003_1140884444) 2,403 European ancestry cases, 453,873 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042239 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dihydrocodeine (UKB data field 20003_1140884464) 1,627 European ancestry cases, 454,649 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042240 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - diclofenac (UKB data field 20003_1140884488) 9,519 European ancestry cases, 446,757 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042241 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - liothyronine (UKB data field 20003_1140884512) 107 European ancestry cases, 456,169 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042242 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - thyroxine product (UKB data field 20003_1140884516) 5,364 European ancestry cases, 450,912 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042243 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nefopam (UKB data field 20003_1140884560) 112 European ancestry cases, 456,164 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042244 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - metformin (UKB data field 20003_1140884600) 11,358 European ancestry cases, 444,918 European ancestry controls NA NR [11842647] (imputed) 3 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042245 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oestrogen product (UKB data field 20003_1140884622) 190 European ancestry cases, 247,318 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042246 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - beclomethasone (UKB data field 20003_1140884654) 1,802 European ancestry cases, 454,474 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042247 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fludrocortisone (UKB data field 20003_1140884672) 192 European ancestry cases, 456,084 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042248 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clobetasone (UKB data field 20003_1140884696) 141 European ancestry cases, 456,135 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042249 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - trimovate ointment (UKB data field 20003_1140884700) 282 European ancestry cases, 455,994 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042250 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - kalms tablet (UKB data field 20003_1140911636) 105 European ancestry cases, 456,171 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042300 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - kelp+garlic product (UKB data field 20003_1140911638) 252 European ancestry cases, 456,024 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042301 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lecithin product (UKB data field 20003_1140911640) 245 European ancestry cases, 456,031 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042302 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tacrolimus (UKB data field 20003_1140911642) 196 European ancestry cases, 456,080 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042303 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - imigran 50mg tablet (UKB data field 20003_1140911658) 744 European ancestry cases, 455,532 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042304 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - starflower oil (UKB data field 20003_1140911680) 708 European ancestry cases, 455,568 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042305 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - selenium ace tablet (UKB data field 20003_1140911682) 602 European ancestry cases, 455,674 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042306 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - slozem 120mg m/r capsule (UKB data field 20003_1140911698) 164 European ancestry cases, 456,112 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042307 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - flax oil tablet (UKB data field 20003_1140911730) 743 European ancestry cases, 455,533 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042308 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - garlic product (UKB data field 20003_1140911732) 6,106 European ancestry cases, 450,170 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042309 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ginkgo forte tablet (UKB data field 20003_1140911734) 2,584 European ancestry cases, 453,692 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042310 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ginseng product (UKB data field 20003_1140911736) 645 European ancestry cases, 455,631 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042311 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - anadin tablet (UKB data field 20003_1140911754) 337 European ancestry cases, 455,939 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042312 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - menophase tablet (UKB data field 20003_1140912212) 121 European ancestry cases, 247,387 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042313 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - venlafaxine (UKB data field 20003_1140916282) 1,856 European ancestry cases, 454,420 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042315 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - efexor 37.5mg tablet (UKB data field 20003_1140916288) 227 European ancestry cases, 456,049 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042316 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - losartan (UKB data field 20003_1140916356) 4,089 European ancestry cases, 452,187 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042317 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - evening primrose oil (UKB data field 20003_1140916682) 7,231 European ancestry cases, 449,045 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042318 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - evorel 25 patch (UKB data field 20003_1140916790) 697 European ancestry cases, 246,811 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042319 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zantac 75 tablet (UKB data field 20003_1140916980) 238 European ancestry cases, 456,038 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042320 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - airomir 100micrograms cfc-free inhaler (UKB data field 20003_1140917034) 206 European ancestry cases, 456,070 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042321 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - kliofem tablet (UKB data field 20003_1140917056) 358 European ancestry cases, 247,150 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042322 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - angitil sr 90 m/r capsule (UKB data field 20003_1140917428) 151 European ancestry cases, 456,125 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042323 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - citalopram (UKB data field 20003_1140921600) 7,804 European ancestry cases, 448,472 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042324 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mirena 52mg intrauterine system (UKB data field 20003_1140921814) 780 European ancestry cases, 246,728 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042325 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - losec 10mg capsule (UKB data field 20003_1140909578) 344 European ancestry cases, 455,932 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042276 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cod liver oil capsule (UKB data field 20003_1140909674) 26,313 European ancestry cases, 429,963 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042277 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sulfasalazine (UKB data field 20003_1140909702) 866 European ancestry cases, 455,410 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042278 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - synalar 1:10 cream (UKB data field 20003_1140913292) 112 European ancestry cases, 456,164 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042314 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - furosemide (UKB data field 20003_1140909708) 3,439 European ancestry cases, 452,837 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042279 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin c product (UKB data field 20003_1140909726) 5,686 European ancestry cases, 450,590 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042280 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - multivitamins capsule (UKB data field 20003_1140909766) 343 European ancestry cases, 455,933 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042281 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - beclometasone (UKB data field 20003_1140909786) 4,138 European ancestry cases, 452,138 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042282 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sodium cromoglicate (UKB data field 20003_1140909788) 356 European ancestry cases, 455,920 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042283 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - chlorphenamine (UKB data field 20003_1140909790) 262 European ancestry cases, 456,014 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042284 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dosulepin (UKB data field 20003_1140909806) 1,603 European ancestry cases, 454,673 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042285 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin b1 preparation (UKB data field 20003_1140909872) 179 European ancestry cases, 456,097 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042286 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin b6 preparation (UKB data field 20003_1140909874) 526 European ancestry cases, 455,750 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042287 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - indometacin (UKB data field 20003_1140909936) 304 European ancestry cases, 455,972 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042288 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - acyclovir (UKB data field 20003_1140909954) 138 European ancestry cases, 456,138 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042289 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - b12 - hydroxocobalamin prep (UKB data field 20003_1140910494) 356 European ancestry cases, 455,920 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042290 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - flu - influenza vaccine (UKB data field 20003_1140910498) 162 European ancestry cases, 456,114 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042291 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ismo - isosorbide mononitrate (UKB data field 20003_1140910512) 154 European ancestry cases, 456,122 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042292 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - iron sulphate (UKB data field 20003_1140910548) 191 European ancestry cases, 456,085 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042293 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - luteine (UKB data field 20003_1140910640) 325 European ancestry cases, 455,951 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042294 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oil of peppermint (UKB data field 20003_1140910698) 135 European ancestry cases, 456,141 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042295 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - phenobarbital (UKB data field 20003_1140910706) 113 European ancestry cases, 456,163 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042296 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nicorandil (UKB data field 20003_1140910766) 1,452 European ancestry cases, 454,824 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042297 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sodium thyroxine (UKB data field 20003_1140910814) 209 European ancestry cases, 456,067 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042298 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sodium warfarin (UKB data field 20003_1140910832) 378 European ancestry cases, 455,898 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042299 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - gamolenic acid (UKB data field 20003_1140880072) 120 European ancestry cases, 456,156 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042201 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcipotriol (UKB data field 20003_1140880086) 278 European ancestry cases, 455,998 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042202 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clotrimazole (UKB data field 20003_1140880288) 105 European ancestry cases, 456,171 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042203 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fentanyl (UKB data field 20003_1140880956) 109 European ancestry cases, 456,167 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042204 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - magnesium carbonate (UKB data field 20003_1140881320) 150 European ancestry cases, 456,126 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042205 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - proctosedyl ointment (UKB data field 20003_1140881446) 180 European ancestry cases, 456,096 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042206 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lacri-lube eye ointment (UKB data field 20003_1140881472) 645 European ancestry cases, 455,631 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042207 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - normacol granules (UKB data field 20003_1140881474) 198 European ancestry cases, 456,078 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042208 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - adalate 10mg capsule (UKB data field 20003_1140881702) 345 European ancestry cases, 455,931 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042209 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salbutamol (UKB data field 20003_1140881856) 5,443 European ancestry cases, 450,833 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042210 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - timoptol 0.25% eye drops (UKB data field 20003_1140881882) 264 European ancestry cases, 456,012 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042211 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-careldopa (UKB data field 20003_1140882112) 104 European ancestry cases, 456,172 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042212 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - seroxat 20mg tablet (UKB data field 20003_1140882236) 599 European ancestry cases, 455,677 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042213 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oramorph 10mg/5ml oral solution (UKB data field 20003_1140882272) 116 European ancestry cases, 456,160 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042214 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - paracetamol + codeine (UKB data field 20003_1140882394) 354 European ancestry cases, 455,922 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042215 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - penicillin (UKB data field 20003_1140882498) 271 European ancestry cases, 456,005 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042216 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - diprosalic ointment (UKB data field 20003_1140882618) 190 European ancestry cases, 456,086 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042217 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - betnesol 0.1% eye/ear/nose drops (UKB data field 20003_1140882626) 136 European ancestry cases, 456,140 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042218 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - betnovate cream (UKB data field 20003_1140882694) 1,555 European ancestry cases, 454,721 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042219 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - otomize ear spray (UKB data field 20003_1140882728) 215 European ancestry cases, 456,061 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042220 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fucibet cream (UKB data field 20003_1140882776) 232 European ancestry cases, 456,044 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042221 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dermovate cream (UKB data field 20003_1140882782) 682 European ancestry cases, 455,594 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042222 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - eumovate cream (UKB data field 20003_1140882800) 484 European ancestry cases, 455,792 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042223 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - daktacort cream (UKB data field 20003_1140882910) 305 European ancestry cases, 455,971 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042224 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - livial 2.5mg tablet (UKB data field 20003_1140882946) 609 European ancestry cases, 246,899 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042225 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clobetasol (UKB data field 20003_1140888074) 110 European ancestry cases, 456,166 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042251 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - elocon cream (UKB data field 20003_1140888092) 297 European ancestry cases, 455,979 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042252 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fluticasone (UKB data field 20003_1140888098) 1,987 European ancestry cases, 454,289 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042253 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mometasone (UKB data field 20003_1140888172) 892 European ancestry cases, 455,384 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042254 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - warfarin (UKB data field 20003_1140888266) 4,588 European ancestry cases, 451,688 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042255 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pyridoxine preparation (UKB data field 20003_1140888362) 135 European ancestry cases, 456,141 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042256 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - thiamine preparation (UKB data field 20003_1140888366) 656 European ancestry cases, 455,620 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042257 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - iron product (UKB data field 20003_1140888386) 1,290 European ancestry cases, 454,986 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042258 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ferrous salt product (UKB data field 20003_1140888390) 136 European ancestry cases, 456,140 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042259 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amiodarone (UKB data field 20003_1140888502) 385 European ancestry cases, 455,891 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042260 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - verapamil (UKB data field 20003_1140888510) 760 European ancestry cases, 455,516 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042261 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amiloride (UKB data field 20003_1140888512) 164 European ancestry cases, 456,112 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042262 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zinc product (UKB data field 20003_1140888538) 3,037 European ancestry cases, 453,239 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042263 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - enalapril (UKB data field 20003_1140888552) 3,484 European ancestry cases, 452,792 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042264 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fosinopril (UKB data field 20003_1140888556) 208 European ancestry cases, 456,068 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042265 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - perindopril (UKB data field 20003_1140888560) 6,523 European ancestry cases, 449,753 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042266 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - flecainide (UKB data field 20003_1140888570) 721 European ancestry cases, 455,555 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042267 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fluvastatin (UKB data field 20003_1140888594) 213 European ancestry cases, 456,063 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042268 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - felodipine (UKB data field 20003_1140888646) 3,838 European ancestry cases, 452,438 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042269 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pravastatin (UKB data field 20003_1140888648) 2,167 European ancestry cases, 454,109 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042270 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - betahistine (UKB data field 20003_1140888688) 1,373 European ancestry cases, 454,903 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042271 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - penicillin v (UKB data field 20003_1140888758) 221 European ancestry cases, 456,055 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042272 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ismn - isosorbide mononitrate (UKB data field 20003_1140888762) 260 European ancestry cases, 456,016 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042273 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - carvedilol (UKB data field 20003_1140909368) 310 European ancestry cases, 455,966 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042274 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - opticrom allergy eye drops (UKB data field 20003_1140909482) 279 European ancestry cases, 455,997 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042275 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace full of chemical or other fumes: PHESANT recoding (UKB data field 22610_1) 27,207 European ancestry cases, 83,961 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043276 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace full of chemical or other fumes: PHESANT recoding (UKB data field 22610_2) 7,454 European ancestry cases, 103,298 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043277 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace had a lot of cigarette smoke from other people smoking: Rarely/never (UKB data field 22611_0) 96,495 European ancestry cases, 16,801 European ancestry controls NA NR [11842647] (imputed) 0 environmental tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0008361 GCST90043278 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace had a lot of cigarette smoke from other people smoking: PHESANT recoding (UKB data field 22611_1) 56,437 European ancestry cases, 56,174 European ancestry controls NA NR [11842647] (imputed) 0 environmental tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0008361 GCST90043279 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace had a lot of cigarette smoke from other people smoking: PHESANT recoding (UKB data field 22611_2) 18,976 European ancestry cases, 93,167 European ancestry controls NA NR [11842647] (imputed) 0 environmental tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0008361 GCST90043280 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with materials containing asbestos: Rarely/never (UKB data field 22612_0) 104,237 European ancestry cases, 2,678 European ancestry controls NA NR [11842647] (imputed) 0 asbestos exposure measurement http://www.ebi.ac.uk/efo/EFO_0004806 GCST90043281 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with materials containing asbestos: PHESANT recoding (UKB data field 22612_1) 10,467 European ancestry cases, 85,989 European ancestry controls NA NR [11842647] (imputed) 0 asbestos exposure measurement http://www.ebi.ac.uk/efo/EFO_0004806 GCST90043282 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with materials containing asbestos: PHESANT recoding (UKB data field 22612_2) 1,652 European ancestry cases, 93,648 European ancestry controls NA NR [11842647] (imputed) 0 asbestos exposure measurement http://www.ebi.ac.uk/efo/EFO_0004806 GCST90043283 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with paints, thinners or glues: Rarely/never (UKB data field 22613_0) 108,382 European ancestry cases, 4,493 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043284 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with paints, thinners or glues: PHESANT recoding (UKB data field 22613_1) 17,690 European ancestry cases, 93,414 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043285 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with paints, thinners or glues: PHESANT recoding (UKB data field 22613_2) 4,660 European ancestry cases, 106,081 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043286 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with pesticides: Rarely/never (UKB data field 22614_0) 111,895 European ancestry cases, 685 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043287 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with pesticides: PHESANT recoding (UKB data field 22614_1) 4,281 European ancestry cases, 105,756 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043288 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worked with pesticides: PHESANT recoding (UKB data field 22614_2) 661 European ancestry cases, 109,202 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043289 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace had a lot of diesel exhaust: Rarely/never (UKB data field 22615_0) 109,466 European ancestry cases, 3,382 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043290 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace had a lot of diesel exhaust: PHESANT recoding (UKB data field 22615_1) 16,422 European ancestry cases, 95,055 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043291 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Workplace had a lot of diesel exhaust: PHESANT recoding (UKB data field 22615_2) 4,413 European ancestry cases, 106,799 European ancestry controls NA NR [11842647] (imputed) 0 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90043292 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breathing problems during period of job: No (UKB data field 22616_0) 111,877 European ancestry cases, 1,964 European ancestry controls NA NR [11842647] (imputed) 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90043293 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breathing problems during period of job: Yes (UKB data field 22616_1) 8,382 European ancestry cases, 105,459 European ancestry controls NA NR [11842647] (imputed) 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90043294 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Senior officials in national government (UKB data field 22617_1111) 1,065 European ancestry cases, 112,776 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043295 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Directors and chief executives of major organisations (UKB data field 22617_1112) 3,448 European ancestry cases, 110,393 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043296 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Senior officials in local government (UKB data field 22617_1113) 1,550 European ancestry cases, 112,291 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043297 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Senior officials of special interest organisations (UKB data field 22617_1114) 2,647 European ancestry cases, 111,194 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043298 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Production, works and maintenance managers (UKB data field 22617_1121) 1,135 European ancestry cases, 112,706 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043299 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Managers in construction (UKB data field 22617_1122) 1,296 European ancestry cases, 112,545 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043300 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Conference and exhibition managers (UKB data field 22617_1222) 137 European ancestry cases, 113,704 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043326 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Restaurant and catering managers (UKB data field 22617_1223) 749 European ancestry cases, 113,092 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043327 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Publicans and managers of licensed premises (UKB data field 22617_1224) 516 European ancestry cases, 113,325 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043328 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Leisure and sports managers (UKB data field 22617_1225) 436 European ancestry cases, 113,405 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043329 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Travel agency managers (UKB data field 22617_1226) 228 European ancestry cases, 113,613 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043330 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Property, housing and land managers (UKB data field 22617_1231) 440 European ancestry cases, 113,401 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043331 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Garage managers and proprietors (UKB data field 22617_1232) 276 European ancestry cases, 113,565 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043332 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Hairdressing and beauty salon managers and proprietors (UKB data field 22617_1233) 339 European ancestry cases, 113,502 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043333 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Shopkeepers and wholesale/retail dealers (UKB data field 22617_1234) 1,884 European ancestry cases, 111,957 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043334 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Managers and proprietors in other services n.e.c. (UKB data field 22617_1239) 124 European ancestry cases, 113,717 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043335 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Chemists (UKB data field 22617_2111) 1,318 European ancestry cases, 112,523 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043336 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Biological scientists and biochemists (UKB data field 22617_2112) 1,324 European ancestry cases, 112,517 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043337 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Physicists, geologists and meteorologists (UKB data field 22617_2113) 892 European ancestry cases, 112,949 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043338 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Civil engineers (UKB data field 22617_2121) 1,135 European ancestry cases, 112,706 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043339 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Mechanical engineers (UKB data field 22617_2122) 1,978 European ancestry cases, 111,863 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043340 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Electrical engineers (UKB data field 22617_2123) 847 European ancestry cases, 112,994 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043341 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Electronics engineers (UKB data field 22617_2124) 1,110 European ancestry cases, 112,731 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043342 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Chemical engineers (UKB data field 22617_2125) 306 European ancestry cases, 113,535 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043343 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Design and development engineers (UKB data field 22617_2126) 739 European ancestry cases, 113,102 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043344 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Production and process engineers (UKB data field 22617_2127) 577 European ancestry cases, 113,264 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043345 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Planning and quality control engineers (UKB data field 22617_2128) 400 European ancestry cases, 113,441 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043346 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Engineering professionals n.e.c. (UKB data field 22617_2129) 937 European ancestry cases, 112,904 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043347 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: IT strategy and planning professionals (UKB data field 22617_2131) 2,273 European ancestry cases, 111,568 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043348 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Software professionals (UKB data field 22617_2132) 4,350 European ancestry cases, 109,491 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043349 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Medical practitioners (UKB data field 22617_2211) 1,872 European ancestry cases, 111,969 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043350 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Public service administrative professionals (UKB data field 22617_2441) 1,655 European ancestry cases, 112,186 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043376 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Social workers (UKB data field 22617_2442) 1,962 European ancestry cases, 111,879 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043377 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Probation officers (UKB data field 22617_2443) 305 European ancestry cases, 113,536 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043378 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Clergy (UKB data field 22617_2444) 653 European ancestry cases, 113,188 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043379 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Librarians (UKB data field 22617_2451) 1,519 European ancestry cases, 112,322 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043380 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Archivists and curators (UKB data field 22617_2452) 349 European ancestry cases, 113,492 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043381 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Laboratory technicians (UKB data field 22617_3111) 3,220 European ancestry cases, 110,621 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043382 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Electrical/electronics technicians (UKB data field 22617_3112) 1,186 European ancestry cases, 112,655 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043383 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Engineering technicians (UKB data field 22617_3113) 1,298 European ancestry cases, 112,543 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043384 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Building and civil engineering technicians (UKB data field 22617_3114) 156 European ancestry cases, 113,685 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043385 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Quality assurance technicians (UKB data field 22617_3115) 443 European ancestry cases, 113,398 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043386 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Science and engineering technicians n.e.c. (UKB data field 22617_3119) 2,518 European ancestry cases, 111,323 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043387 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Architectural technologists and town planning technicians (UKB data field 22617_3121) 219 European ancestry cases, 113,622 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043388 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Draughtspersons (UKB data field 22617_3122) 358 European ancestry cases, 113,483 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043389 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: IT operations technicians (UKB data field 22617_3131) 1,378 European ancestry cases, 112,463 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043390 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: IT user support technicians (UKB data field 22617_3132) 899 European ancestry cases, 112,942 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043391 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Nurses (UKB data field 22617_3211) 6,348 European ancestry cases, 107,493 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043392 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Midwives (UKB data field 22617_3212) 935 European ancestry cases, 112,906 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043393 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Paramedics (UKB data field 22617_3213) 122 European ancestry cases, 113,719 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043394 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Medical radiographers (UKB data field 22617_3214) 176 European ancestry cases, 113,665 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043395 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Chiropodists (UKB data field 22617_3215) 158 European ancestry cases, 113,683 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043396 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Pharmaceutical dispensers (UKB data field 22617_3217) 204 European ancestry cases, 113,637 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043397 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Medical and dental technicians (UKB data field 22617_3218) 468 European ancestry cases, 113,373 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043398 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Physiotherapists (UKB data field 22617_3221) 597 European ancestry cases, 113,244 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043399 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Occupational therapists (UKB data field 22617_3222) 371 European ancestry cases, 113,470 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043400 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Estimators, valuers and assessors (UKB data field 22617_3531) 580 European ancestry cases, 113,261 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043426 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Brokers (UKB data field 22617_3532) 832 European ancestry cases, 113,009 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043427 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Insurance underwriters (UKB data field 22617_3533) 630 European ancestry cases, 113,211 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043428 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Finance and investment analysts/advisers (UKB data field 22617_3534) 1,093 European ancestry cases, 112,748 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043429 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Taxation experts (UKB data field 22617_3535) 309 European ancestry cases, 113,532 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043430 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Importers, exporters (UKB data field 22617_3536) 194 European ancestry cases, 113,647 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043431 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Financial and accounting technicians (UKB data field 22617_3537) 1,904 European ancestry cases, 111,937 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043432 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Business and related associate professionals n.e.c. (UKB data field 22617_3539) 2,428 European ancestry cases, 111,413 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043433 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Buyers and purchasing officers (UKB data field 22617_3541) 533 European ancestry cases, 113,308 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043434 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Sales representatives (UKB data field 22617_3542) 1,404 European ancestry cases, 112,437 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043435 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Marketing associate professionals (UKB data field 22617_3543) 837 European ancestry cases, 113,004 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043436 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Estate agents, auctioneers (UKB data field 22617_3544) 363 European ancestry cases, 113,478 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043437 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Public service associate professionals (UKB data field 22617_3561) 4,051 European ancestry cases, 109,790 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043438 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Personnel and industrial relations officers (UKB data field 22617_3562) 1,817 European ancestry cases, 112,024 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043439 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Vocational and industrial trainers and instructors (UKB data field 22617_3563) 1,259 European ancestry cases, 112,582 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043440 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Careers advisers and vocational guidance specialists (UKB data field 22617_3564) 526 European ancestry cases, 113,315 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043441 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Inspectors of factories, utilities and trading standards (UKB data field 22617_3565) 120 European ancestry cases, 113,721 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043442 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Occupational hygienists and safety officers (health and safety) (UKB data field 22617_3567) 433 European ancestry cases, 113,408 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043443 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Civil Service executive officers (UKB data field 22617_4111) 4,298 European ancestry cases, 109,543 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043444 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Civil Service administrative officers and assistants (UKB data field 22617_4112) 5,133 European ancestry cases, 108,708 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043445 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Local government clerical officers and assistants (UKB data field 22617_4113) 6,056 European ancestry cases, 107,785 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043446 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Officers of non-governmental organisations (UKB data field 22617_4114) 2,023 European ancestry cases, 111,818 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043447 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Credit controllers (UKB data field 22617_4121) 498 European ancestry cases, 113,343 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043448 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Accounts and wages clerks, book-keepers, other financial clerks (UKB data field 22617_4122) 3,478 European ancestry cases, 110,363 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043449 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Counter clerks (UKB data field 22617_4123) 3,873 European ancestry cases, 109,968 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043450 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Speech and language therapists (UKB data field 22617_3223) 189 European ancestry cases, 113,652 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043401 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Therapists n.e.c. (UKB data field 22617_3229) 1,133 European ancestry cases, 112,708 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043402 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Youth and community workers (UKB data field 22617_3231) 1,374 European ancestry cases, 112,467 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043403 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Housing and welfare officers (UKB data field 22617_3232) 642 European ancestry cases, 113,199 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043404 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: NCOs and other ranks (UKB data field 22617_3311) 2,549 European ancestry cases, 111,292 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043405 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Police officers (sergeant and below) (UKB data field 22617_3312) 1,445 European ancestry cases, 112,396 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043406 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Fire service officers (leading fire officer and below) (UKB data field 22617_3313) 243 European ancestry cases, 113,598 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043407 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Prison service officers (below principal officer) (UKB data field 22617_3314) 138 European ancestry cases, 113,703 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043408 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Protective service associate professionals n.e.c. (UKB data field 22617_3319) 172 European ancestry cases, 113,669 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043409 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Artists (UKB data field 22617_3411) 252 European ancestry cases, 113,589 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043410 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Authors, writers (UKB data field 22617_3412) 405 European ancestry cases, 113,436 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043411 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Actors, entertainers (UKB data field 22617_3413) 240 European ancestry cases, 113,601 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043412 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Musicians (UKB data field 22617_3415) 208 European ancestry cases, 113,633 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043413 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Arts officers, producers and directors (UKB data field 22617_3416) 324 European ancestry cases, 113,517 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043414 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Graphic designers (UKB data field 22617_3421) 418 European ancestry cases, 113,423 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043415 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Product, clothing and related designers (UKB data field 22617_3422) 304 European ancestry cases, 113,537 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043416 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Journalists, newspaper and periodical editors (UKB data field 22617_3431) 630 European ancestry cases, 113,211 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043417 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Broadcasting associate professionals (UKB data field 22617_3432) 502 European ancestry cases, 113,339 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043418 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Public relations officers (UKB data field 22617_3433) 661 European ancestry cases, 113,180 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043419 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Photographers and audio-visual equipment operators (UKB data field 22617_3434) 528 European ancestry cases, 113,313 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043420 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Sports coaches, instructors and officials (UKB data field 22617_3442) 295 European ancestry cases, 113,546 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043421 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Fitness instructors (UKB data field 22617_3443) 101 European ancestry cases, 113,740 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043422 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Aircraft pilots and flight engineers (UKB data field 22617_3512) 137 European ancestry cases, 113,704 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043423 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Ship and hovercraft officers (UKB data field 22617_3513) 426 European ancestry cases, 113,415 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043424 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Legal associate professionals (UKB data field 22617_3520) 180 European ancestry cases, 113,661 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043425 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Managers in mining and energy (UKB data field 22617_1123) 395 European ancestry cases, 113,446 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043301 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Financial managers and chartered secretaries (UKB data field 22617_1131) 321 European ancestry cases, 113,520 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043302 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Marketing and sales managers (UKB data field 22617_1132) 2,751 European ancestry cases, 111,090 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043303 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Purchasing managers (UKB data field 22617_1133) 334 European ancestry cases, 113,507 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043304 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Advertising and public relations managers (UKB data field 22617_1134) 760 European ancestry cases, 113,081 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043305 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Personnel, training and industrial relations managers (UKB data field 22617_1135) 1,419 European ancestry cases, 112,422 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043306 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Information and communication technology managers (UKB data field 22617_1136) 2,032 European ancestry cases, 111,809 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043307 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Research and development managers (UKB data field 22617_1137) 1,570 European ancestry cases, 112,271 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043308 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Quality assurance managers (UKB data field 22617_1141) 497 European ancestry cases, 113,344 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043309 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Customer care managers (UKB data field 22617_1142) 660 European ancestry cases, 113,181 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043310 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Financial institution managers (UKB data field 22617_1151) 1,617 European ancestry cases, 112,224 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043311 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Office managers (UKB data field 22617_1152) 1,408 European ancestry cases, 112,433 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043312 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Transport and distribution managers (UKB data field 22617_1161) 633 European ancestry cases, 113,208 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043313 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Storage and warehouse managers (UKB data field 22617_1162) 225 European ancestry cases, 113,616 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043314 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Retail and wholesale managers (UKB data field 22617_1163) 2,212 European ancestry cases, 111,629 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043315 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Officers in armed forces (UKB data field 22617_1171) 723 European ancestry cases, 113,118 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043316 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Police officers (inspectors and above) (UKB data field 22617_1172) 448 European ancestry cases, 113,393 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043317 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Senior officers in fire, ambulance, prison and related services (UKB data field 22617_1173) 290 European ancestry cases, 113,551 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043318 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Security managers (UKB data field 22617_1174) 108 European ancestry cases, 113,733 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043319 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Hospital and health service managers (UKB data field 22617_1181) 1,211 European ancestry cases, 112,630 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043320 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Healthcare practice managers (UKB data field 22617_1183) 224 European ancestry cases, 113,617 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043321 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Social services managers (UKB data field 22617_1184) 958 European ancestry cases, 112,883 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043322 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Residential and day care managers (UKB data field 22617_1185) 496 European ancestry cases, 113,345 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043323 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Farm managers (UKB data field 22617_1211) 203 European ancestry cases, 113,638 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043324 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Hotel and accommodation managers (UKB data field 22617_1221) 523 European ancestry cases, 113,318 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043325 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Psychologists (UKB data field 22617_2212) 366 European ancestry cases, 113,475 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043351 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Pharmacists/pharmacologists (UKB data field 22617_2213) 487 European ancestry cases, 113,354 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043352 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Ophthalmic opticians (UKB data field 22617_2214) 132 European ancestry cases, 113,709 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043353 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Dental practitioners (UKB data field 22617_2215) 357 European ancestry cases, 113,484 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043354 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Veterinarians (UKB data field 22617_2216) 121 European ancestry cases, 113,720 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043355 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Higher education teaching professionals (UKB data field 22617_2311) 3,909 European ancestry cases, 109,932 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043356 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Further education teaching professionals (UKB data field 22617_2312) 3,117 European ancestry cases, 110,724 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043357 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Education officers, school inspectors (UKB data field 22617_2313) 1,316 European ancestry cases, 112,525 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043358 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Secondary education teaching professionals (UKB data field 22617_2314) 9,516 European ancestry cases, 104,325 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043359 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Primary and nursery education teaching professionals (UKB data field 22617_2315) 6,990 European ancestry cases, 106,851 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043360 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Special needs education teaching professionals (UKB data field 22617_2316) 1,490 European ancestry cases, 112,351 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043361 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Registrars and senior administrators of educational establishments (UKB data field 22617_2317) 1,780 European ancestry cases, 112,061 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043362 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Teaching professionals n.e.c. (UKB data field 22617_2319) 2,040 European ancestry cases, 111,801 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043363 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Scientific researchers (UKB data field 22617_2321) 1,466 European ancestry cases, 112,375 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043364 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Social science researchers (UKB data field 22617_2322) 578 European ancestry cases, 113,263 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043365 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Researchers n.e.c. (UKB data field 22617_2329) 1,291 European ancestry cases, 112,550 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043366 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Solicitors and lawyers, judges and coroners (UKB data field 22617_2411) 1,339 European ancestry cases, 112,502 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043367 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Legal professionals n.e.c. (UKB data field 22617_2419) 229 European ancestry cases, 113,612 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043368 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Chartered and certified accountants (UKB data field 22617_2421) 2,418 European ancestry cases, 111,423 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043369 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Management accountants (UKB data field 22617_2422) 958 European ancestry cases, 112,883 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043370 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Management consultants, actuaries, economists and statisticians (UKB data field 22617_2423) 1,318 European ancestry cases, 112,523 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043371 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Architects (UKB data field 22617_2431) 966 European ancestry cases, 112,875 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043372 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Town planners (UKB data field 22617_2432) 274 European ancestry cases, 113,567 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043373 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Quantity surveyors (UKB data field 22617_2433) 528 European ancestry cases, 113,313 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043374 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Chartered surveyors (not quantity surveyors) (UKB data field 22617_2434) 964 European ancestry cases, 112,877 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043375 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of hair and hair follicles (PheCode 704) 5,290 European ancestry cases, 451,058 European ancestry controls NA NR [11842647] (imputed) 0 disorder of pilosebaceous unit http://purl.obolibrary.org/obo/MONDO_0002917 GCST90044529 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hidradenitis (PheCode 705.3) 174 European ancestry cases, 456,174 European ancestry controls NA NR [11842647] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90044530 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hyperhidrosis (PheCode 705.8) 165 European ancestry cases, 456,183 European ancestry controls NA NR [11842647] (imputed) 0 Hyperhidrosis http://purl.obolibrary.org/obo/HP_0000975 GCST90044531 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sebaceous cyst (PheCode 706.2) 8,581 European ancestry cases, 447,767 European ancestry controls NA NR [11842647] (imputed) 0 Epidermal Inclusion Cyst http://www.ebi.ac.uk/efo/EFO_1000243 GCST90044532 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic ulcer of skin (PheCode 707) 495 European ancestry cases, 455,853 European ancestry controls NA NR [11842647] (imputed) 0 chronic ulcer of skin http://www.ebi.ac.uk/efo/EFO_0007066 GCST90044533 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sicca syndrome (PheCode 709.2) 99 European ancestry cases, 456,249 European ancestry controls NA NR [11842647] (imputed) 0 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90044534 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Systemic sclerosis (PheCode 709.3) 104 European ancestry cases, 456,244 European ancestry controls NA NR [11842647] (imputed) 0 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST90044535 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Unspecified diffuse connective tissue disease (PheCode 709.7) 2,600 European ancestry cases, 453,748 European ancestry controls NA NR [11842647] (imputed) 0 connective tissue disease http://www.ebi.ac.uk/efo/EFO_1001986 GCST90044536 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic osteomyelitis (PheCode 710.12) 123 European ancestry cases, 456,225 European ancestry controls NA NR [11842647] (imputed) 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90044537 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Unspecified osteomyelitis (PheCode 710.19) 269 European ancestry cases, 456,079 European ancestry controls NA NR [11842647] (imputed) 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90044538 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pyogenic arthritis (PheCode 711.1) 305 European ancestry cases, 456,043 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044539 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rheumatoid arthritis (PheCode 714.1) 1,961 European ancestry cases, 454,387 European ancestry controls NA NR [11842647] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90044540 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rheumatoid arthritis and other inflammatory polyarthropathies (PheCode 714) 232 European ancestry cases, 456,116 European ancestry controls NA NR [11842647] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90044541 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ankylosing spondylitis (PheCode 715.2) 186 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90044542 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other inflammatory spondylopathies (PheCode 715) 149 European ancestry cases, 456,199 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044543 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Unspecified monoarthritis (PheCode 716.2) 11,069 European ancestry cases, 445,279 European ancestry controls NA NR [11842647] (imputed) 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90044544 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Arthropathy, not otherwise specified (PheCode 716.9) 17,266 European ancestry cases, 439,082 European ancestry controls NA NR [11842647] (imputed) 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90044545 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Polymyalgia Rheumatica (PheCode 717) 122 European ancestry cases, 456,226 European ancestry controls NA NR [11842647] (imputed) 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90044546 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spinal stenosis (PheCode 720) 2,389 European ancestry cases, 453,959 European ancestry controls NA NR [11842647] (imputed) 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90044547 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spondylosis without myelopathy (PheCode 721.1) 2,044 European ancestry cases, 454,304 European ancestry controls NA NR [11842647] (imputed) 0 spondyloarthropathy http://www.ebi.ac.uk/efo/EFO_0000706 GCST90044548 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spondylosis with myelopathy (PheCode 721.2) 159 European ancestry cases, 456,189 European ancestry controls NA NR [11842647] (imputed) 0 spondyloarthropathy http://www.ebi.ac.uk/efo/EFO_0000706 GCST90044549 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other allied disorders of spine (PheCode 721.8) 103 European ancestry cases, 456,245 European ancestry controls NA NR [11842647] (imputed) 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90044550 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spondylosis and allied disorders (PheCode 721) 823 European ancestry cases, 455,525 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044551 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Displacement of intervertebral disc (PheCode 722.1) 225 European ancestry cases, 456,123 European ancestry controls NA NR [11842647] (imputed) 0 Intervertebral Disc Displacement http://www.ebi.ac.uk/efo/EFO_1001800 GCST90044552 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Degeneration of intervertebral disc (PheCode 722.6) 1,691 European ancestry cases, 454,657 European ancestry controls NA NR [11842647] (imputed) 0 Intervertebral disc degeneration http://purl.obolibrary.org/obo/HP_0008419 GCST90044553 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital anomalies of great vessels (PheCode 747.13) 919 European ancestry cases, 455,429 European ancestry controls NA NR [11842647] (imputed) 0 congenital anomaly of the great arteries http://purl.obolibrary.org/obo/MONDO_0020292 GCST90044604 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital anomalies of peripheral vascular system (PheCode 747.2) 140 European ancestry cases, 456,208 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the vasculature http://purl.obolibrary.org/obo/HP_0002597 GCST90044605 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital anomalies of face and neck (PheCode 749) 231 European ancestry cases, 456,117 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal nasolacrimal system morphology http://purl.obolibrary.org/obo/HP_0000614 GCST90044606 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital anomalies of mouth/tongue (PheCode 750.13) 171 European ancestry cases, 456,177 European ancestry controls NA NR [11842647] (imputed) 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90044607 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital anomalies of female genital organs (PheCode 751.11) 134 European ancestry cases, 247,406 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal morphology of female internal genitalia http://purl.obolibrary.org/obo/HP_0000008 GCST90044608 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital anomalies of male genital organs (PheCode 751.12) 94 European ancestry cases, 208,714 European ancestry controls NA NR [11842647] (imputed) 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90044609 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital deformities of feet (PheCode 755.1) 119 European ancestry cases, 456,229 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal foot morphology http://purl.obolibrary.org/obo/HP_0001760 GCST90044610 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Congenital osteodystrophies (PheCode 756.5) 224 European ancestry cases, 456,124 European ancestry controls NA NR [11842647] (imputed) 0 bone development disease http://www.ebi.ac.uk/efo/EFO_0005541 GCST90044611 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Back pain (PheCode 760) 8,860 European ancestry cases, 447,488 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044612 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cervicalgia (PheCode 761) 1,321 European ancestry cases, 455,027 European ancestry controls NA NR [11842647] (imputed) 0 Neck pain http://purl.obolibrary.org/obo/HP_0030833 GCST90044613 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sciatica (PheCode 764) 1,502 European ancestry cases, 454,846 European ancestry controls NA NR [11842647] (imputed) 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90044614 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cervical radiculitis (PheCode 765) 444 European ancestry cases, 455,904 European ancestry controls NA NR [11842647] (imputed) 0 radiculitis http://purl.obolibrary.org/obo/MONDO_0021765 GCST90044615 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neuralgia, neuritis, and radiculitis, not otherwise specified (PheCode 766) 945 European ancestry cases, 455,403 European ancestry controls NA NR [11842647] (imputed) 0 peripheral neuropathy http://www.ebi.ac.uk/efo/EFO_0003100 GCST90044616 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Myalgia and myositis unspecified (PheCode 770) 437 European ancestry cases, 455,911 European ancestry controls NA NR [11842647] (imputed) 0 myositis http://www.ebi.ac.uk/efo/EFO_0000783 GCST90044617 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Swelling of limb (PheCode 771.1) 3,607 European ancestry cases, 452,741 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of limbs http://purl.obolibrary.org/obo/HP_0040064 GCST90044618 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Musculoskeletal symptoms referable to limbs (PheCode 771) 737 European ancestry cases, 455,611 European ancestry controls NA NR [11842647] (imputed) 0 musculoskeletal system disease http://www.ebi.ac.uk/efo/EFO_0009676 GCST90044619 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms of the muscles (PheCode 772) 363 European ancestry cases, 455,985 European ancestry controls NA NR [11842647] (imputed) 0 muscular disease http://www.ebi.ac.uk/efo/EFO_0002970 GCST90044620 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain in limb (PheCode 773) 4,693 European ancestry cases, 451,655 European ancestry controls NA NR [11842647] (imputed) 0 Limb pain http://purl.obolibrary.org/obo/HP_0009763 GCST90044621 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms involving nervous and musculoskeletal systems (PheCode 781) 1,071 European ancestry cases, 455,277 European ancestry controls NA NR [11842647] (imputed) 0 musculoskeletal system disease, nervous system disease http://www.ebi.ac.uk/efo/EFO_0009676, http://www.ebi.ac.uk/efo/EFO_0000618 GCST90044622 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Edema (PheCode 782.3) 311 European ancestry cases, 456,037 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044623 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fever of unknown origin (PheCode 783) 1,455 European ancestry cases, 454,893 European ancestry controls NA NR [11842647] (imputed) 0 fever of unknown origin http://www.ebi.ac.uk/efo/EFO_0003952 GCST90044624 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abdominal pain (PheCode 785) 35,233 European ancestry cases, 421,115 European ancestry controls NA NR [11842647] (imputed) 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90044625 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Syncope and collapse (PheCode 788) 6,830 European ancestry cases, 449,518 European ancestry controls NA NR [11842647] (imputed) 0 Syncope http://purl.obolibrary.org/obo/HP_0001279 GCST90044626 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nausea and vomiting (PheCode 789) 3,072 European ancestry cases, 453,276 European ancestry controls NA NR [11842647] (imputed) 0 Nausea and vomiting http://purl.obolibrary.org/obo/HP_0002017 GCST90044627 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other abnormal blood chemistry (PheCode 790.6) 3,313 European ancestry cases, 453,035 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of blood and blood-forming tissues http://purl.obolibrary.org/obo/HP_0001871 GCST90044628 Genome-wide genotyping array 2022-05-06 35459240 Said S 2022-04-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35459240 Genetic analysis of over half a million people characterises C-reactive protein loci. C-reactive protein levels 575,531 European ancestry individuals NA NR [11106737] (imputed) 266 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90029070 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hallux rigidus (PheCode 735.23) 1,444 European ancestry cases, 454,904 European ancestry controls NA NR [11842647] (imputed) 0 Hallux rigidus http://purl.obolibrary.org/obo/HP_0025004 GCST90044579 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acquired toe deformities (PheCode 735.2) 1,402 European ancestry cases, 454,946 European ancestry controls NA NR [11842647] (imputed) 0 leg injury http://www.ebi.ac.uk/efo/EFO_0009508 GCST90044580 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hallux valgus (Bunion) (PheCode 735.3) 6,918 European ancestry cases, 449,430 European ancestry controls NA NR [11842647] (imputed) 0 Hallux valgus http://purl.obolibrary.org/obo/HP_0001822 GCST90044581 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acquired foot deformities (PheCode 735) 141 European ancestry cases, 456,207 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal foot morphology http://purl.obolibrary.org/obo/HP_0001760 GCST90044582 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acquired deformities of finger (PheCode 736.2) 217 European ancestry cases, 456,131 European ancestry controls NA NR [11842647] (imputed) 0 limb injury http://www.ebi.ac.uk/efo/EFO_0009509 GCST90044583 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other acquired deformities of limbs (PheCode 736) 564 European ancestry cases, 455,784 European ancestry controls NA NR [11842647] (imputed) 0 congenital deformities of limbs http://purl.obolibrary.org/obo/MONDO_0017427 GCST90044584 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Kyphoscoliosis and scoliosis (PheCode 737.3) 266 European ancestry cases, 456,082 European ancestry controls NA NR [11842647] (imputed) 0 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST90044585 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acquired spondylolisthesis (PheCode 738.4) 823 European ancestry cases, 455,525 European ancestry controls NA NR [11842647] (imputed) 0 spondylolisthesis http://www.ebi.ac.uk/efo/EFO_0007493 GCST90044586 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other acquired musculoskeletal deformity (PheCode 738) 274 European ancestry cases, 456,074 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044587 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Contracture of joint (PheCode 739) 312 European ancestry cases, 456,036 European ancestry controls NA NR [11842647] (imputed) 0 contracture http://www.ebi.ac.uk/efo/EFO_0003899 GCST90044588 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteoarthrosis, localized, primary (PheCode 740.11) 8,439 European ancestry cases, 447,909 European ancestry controls NA NR [11842647] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90044589 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteoarthrosis, localized, secondary (PheCode 740.12) 288 European ancestry cases, 456,060 European ancestry controls NA NR [11842647] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90044590 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteoarthritis; localized (PheCode 740.1) 8,952 European ancestry cases, 447,396 European ancestry controls NA NR [11842647] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90044591 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteoarthrosis, generalized (PheCode 740.2) 346 European ancestry cases, 456,002 European ancestry controls NA NR [11842647] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90044592 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteoarthrosis, not otherwise specified (PheCode 740.9) 2,227 European ancestry cases, 454,121 European ancestry controls NA NR [11842647] (imputed) 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90044593 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Stiffness of joint (PheCode 741.2) 488 European ancestry cases, 455,860 European ancestry controls NA NR [11842647] (imputed) 0 Joint stiffness http://purl.obolibrary.org/obo/HP_0001387 GCST90044594 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Joint effusions (PheCode 741.4) 763 European ancestry cases, 455,585 European ancestry controls NA NR [11842647] (imputed) 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90044595 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms and disorders of the joints (PheCode 741) 747 European ancestry cases, 455,601 European ancestry controls NA NR [11842647] (imputed) 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90044596 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Loose body in joint (PheCode 742.1) 195 European ancestry cases, 456,153 European ancestry controls NA NR [11842647] (imputed) 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90044597 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Articular cartilage disorder (PheCode 742.8) 484 European ancestry cases, 455,864 European ancestry controls NA NR [11842647] (imputed) 0 articular cartilage disorder http://purl.obolibrary.org/obo/MONDO_0003816 GCST90044598 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other derangement of joint (PheCode 742.9) 1,739 European ancestry cases, 454,609 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044599 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteoporosis, not otherwise specified (PheCode 743.11) 991 European ancestry cases, 455,357 European ancestry controls NA NR [11842647] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90044600 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteopenia or other disorder of bone and cartilage (PheCode 743.9) 610 European ancestry cases, 455,738 European ancestry controls NA NR [11842647] (imputed) 0 bone disease, cartilage disease http://www.ebi.ac.uk/efo/EFO_0004260, http://www.ebi.ac.uk/efo/EFO_0005802 GCST90044601 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain in joint (PheCode 745) 6,833 European ancestry cases, 449,515 European ancestry controls NA NR [11842647] (imputed) 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90044602 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cardiac shunt/ heart septal defect (PheCode 747.11) 392 European ancestry cases, 455,956 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal cardiac septum morphology http://purl.obolibrary.org/obo/HP_0001671 GCST90044603 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Intervertebral disc disorder with myelopathy (PheCode 722.7) 375 European ancestry cases, 455,973 European ancestry controls NA NR [11842647] (imputed) 0 Intervertebral disc degeneration http://purl.obolibrary.org/obo/HP_0008419 GCST90044554 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other and unspecified disc disorder (PheCode 722.9) 1,001 European ancestry cases, 455,347 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044555 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of cervical region (PheCode 723) 393 European ancestry cases, 455,955 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the vertebral column http://purl.obolibrary.org/obo/HP_0000925 GCST90044556 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other unspecified back disorders (PheCode 724.9) 416 European ancestry cases, 455,932 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the vertebral column http://purl.obolibrary.org/obo/HP_0000925 GCST90044557 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Enthesopathy (PheCode 726.1) 6,439 European ancestry cases, 449,909 European ancestry controls NA NR [11842647] (imputed) 0 enthesopathy http://www.ebi.ac.uk/efo/EFO_0009666 GCST90044558 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Synoviopathy (PheCode 726.2) 227 European ancestry cases, 456,121 European ancestry controls NA NR [11842647] (imputed) 0 synovium disorder http://purl.obolibrary.org/obo/MONDO_0056799 GCST90044559 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bursitis (PheCode 726.3) 843 European ancestry cases, 455,505 European ancestry controls NA NR [11842647] (imputed) 0 bursitis http://purl.obolibrary.org/obo/MONDO_0002471 GCST90044560 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peripheral enthesopathies and allied syndromes (PheCode 726) 9,969 European ancestry cases, 446,379 European ancestry controls NA NR [11842647] (imputed) 0 enthesopathy http://www.ebi.ac.uk/efo/EFO_0009666 GCST90044561 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Synovitis and tenosynovitis (PheCode 727.1) 3,692 European ancestry cases, 452,656 European ancestry controls NA NR [11842647] (imputed) 0 tenosynovitis http://www.ebi.ac.uk/efo/EFO_1001435 GCST90044562 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ganglion and cyst of synovium, tendon, and bursa (PheCode 727.4) 2,951 European ancestry cases, 453,397 European ancestry controls NA NR [11842647] (imputed) 0 ganglion or cyst of synovium/tendon/bursa http://purl.obolibrary.org/obo/MONDO_0004874 GCST90044563 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rupture of synovium (PheCode 727.5) 452 European ancestry cases, 455,896 European ancestry controls NA NR [11842647] (imputed) 0 synovium disorder http://purl.obolibrary.org/obo/MONDO_0056799 GCST90044564 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rupture of tendon, nontraumatic (PheCode 727.6) 316 European ancestry cases, 456,032 European ancestry controls NA NR [11842647] (imputed) 0 Tendon rupture http://purl.obolibrary.org/obo/HP_0100550 GCST90044565 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Contracture of tendon (sheath) (PheCode 727.7) 102 European ancestry cases, 456,246 European ancestry controls NA NR [11842647] (imputed) 0 tendon sheath disorder http://purl.obolibrary.org/obo/MONDO_0024876 GCST90044566 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of synovium, tendon, and bursa (PheCode 727) 572 European ancestry cases, 455,776 European ancestry controls NA NR [11842647] (imputed) 0 synovium disorder http://purl.obolibrary.org/obo/MONDO_0056799 GCST90044567 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Laxity of ligament or hypermobility syndrome (PheCode 728.2) 282 European ancestry cases, 456,066 European ancestry controls NA NR [11842647] (imputed) 0 hypermobility syndrome http://purl.obolibrary.org/obo/MONDO_0001798 GCST90044568 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Contracture of palmar fascia [Dupuytren's disease] (PheCode 728.71) 3,728 European ancestry cases, 452,620 European ancestry controls NA NR [11842647] (imputed) 0 Palmar Fibromatosis http://www.ebi.ac.uk/efo/EFO_1000438 GCST90044569 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fasciitis (PheCode 728.7) 289 European ancestry cases, 456,059 European ancestry controls NA NR [11842647] (imputed) 0 Fasciitis http://purl.obolibrary.org/obo/HP_0100537 GCST90044570 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rheumatism, unspecified and fibrositis (PheCode 729.1) 188 European ancestry cases, 456,160 European ancestry controls NA NR [11842647] (imputed) 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90044571 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of soft tissues (PheCode 729) 3,969 European ancestry cases, 452,379 European ancestry controls NA NR [11842647] (imputed) 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90044572 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Osteochondropathies (PheCode 732) 106 European ancestry cases, 456,242 European ancestry controls NA NR [11842647] (imputed) 0 bone disease, cartilage disease http://www.ebi.ac.uk/efo/EFO_0004260, http://www.ebi.ac.uk/efo/EFO_0005802 GCST90044573 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aseptic necrosis of bone (PheCode 733.4) 257 European ancestry cases, 456,091 European ancestry controls NA NR [11842647] (imputed) 0 osteonecrosis http://www.ebi.ac.uk/efo/EFO_0004259 GCST90044574 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malunion and nonunion of fracture (PheCode 733.8) 1,177 European ancestry cases, 455,171 European ancestry controls NA NR [11842647] (imputed) 0 malunion fracture http://www.ebi.ac.uk/efo/EFO_0010684 GCST90044575 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of bone and cartilage (PheCode 733) 645 European ancestry cases, 455,703 European ancestry controls NA NR [11842647] (imputed) 0 cartilage disease http://www.ebi.ac.uk/efo/EFO_0005802 GCST90044576 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Flat foot (PheCode 735.1) 102 European ancestry cases, 456,246 European ancestry controls NA NR [11842647] (imputed) 0 flatfoot http://www.ebi.ac.uk/efo/EFO_0003874 GCST90044577 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hammer toe (acquired) (PheCode 735.21) 1,085 European ancestry cases, 455,263 European ancestry controls NA NR [11842647] (imputed) 0 Hammer Toe Syndrome http://www.ebi.ac.uk/efo/EFO_1001336 GCST90044578 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gangrene (PheCode 791) 116 European ancestry cases, 456,232 European ancestry controls NA NR [11842647] (imputed) 0 gangrene http://www.ebi.ac.uk/efo/EFO_0008574 GCST90044629 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nonspecific abnormal findings on radiological and other examination of other intrathoracic organs (echocardiogram, etc) (PheCode 793.2) 220 European ancestry cases, 456,128 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal thorax morphology http://purl.obolibrary.org/obo/HP_0000765 GCST90044630 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malaise and fatigue (PheCode 798) 1,128 European ancestry cases, 455,220 European ancestry controls NA NR [11842647] (imputed) 0 malaise, Fatigue http://www.ebi.ac.uk/efo/EFO_0009641, http://purl.obolibrary.org/obo/HP_0012378 GCST90044631 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of neck of femur (PheCode 800.1) 1,930 European ancestry cases, 454,418 European ancestry controls NA NR [11842647] (imputed) 0 hip fracture, femur fracture http://www.ebi.ac.uk/efo/EFO_0003964, http://www.ebi.ac.uk/efo/EFO_0008553 GCST90044632 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of unspecified part of femur (PheCode 800.2) 850 European ancestry cases, 455,498 European ancestry controls NA NR [11842647] (imputed) 0 femur fracture http://www.ebi.ac.uk/efo/EFO_0008553 GCST90044633 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of tibia and fibula (PheCode 800.3) 2,055 European ancestry cases, 454,293 European ancestry controls NA NR [11842647] (imputed) 0 fibula fracture, tibia fracture http://www.ebi.ac.uk/efo/EFO_0009613, http://www.ebi.ac.uk/efo/EFO_0003944 GCST90044634 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of patella (PheCode 800.4) 677 European ancestry cases, 455,671 European ancestry controls NA NR [11842647] (imputed) 0 knee fracture http://www.ebi.ac.uk/efo/EFO_0009617 GCST90044635 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of lower limb (PheCode 800) 2,881 European ancestry cases, 453,467 European ancestry controls NA NR [11842647] (imputed) 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90044636 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of ankle and foot (PheCode 801) 1,907 European ancestry cases, 454,441 European ancestry controls NA NR [11842647] (imputed) 0 ankle fracture, foot fracture http://www.ebi.ac.uk/efo/EFO_0009615, http://www.ebi.ac.uk/efo/EFO_0009618 GCST90044637 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of pelvis (PheCode 802) 586 European ancestry cases, 455,762 European ancestry controls NA NR [11842647] (imputed) 0 fracture of pelvis http://www.ebi.ac.uk/efo/EFO_0009622 GCST90044638 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of humerus (PheCode 803.1) 1,662 European ancestry cases, 454,686 European ancestry controls NA NR [11842647] (imputed) 0 humerus fracture http://www.ebi.ac.uk/efo/EFO_0003943 GCST90044639 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of radius and ulna (PheCode 803.2) 5,587 European ancestry cases, 450,761 European ancestry controls NA NR [11842647] (imputed) 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90044640 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of clavicle or scapula (PheCode 803.3) 1,000 European ancestry cases, 455,348 European ancestry controls NA NR [11842647] (imputed) 0 shoulder fracture, clavicle fracture http://www.ebi.ac.uk/efo/EFO_0009621, http://www.ebi.ac.uk/efo/EFO_0009614 GCST90044641 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of upper limb (PheCode 803) 297 European ancestry cases, 456,051 European ancestry controls NA NR [11842647] (imputed) 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90044642 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of hand or wrist (PheCode 804) 3,030 European ancestry cases, 453,318 European ancestry controls NA NR [11842647] (imputed) 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90044643 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of vertebral column without mention of spinal cord injury (PheCode 805) 1,258 European ancestry cases, 455,090 European ancestry controls NA NR [11842647] (imputed) 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90044644 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of ribs (PheCode 807) 802 European ancestry cases, 455,546 European ancestry controls NA NR [11842647] (imputed) 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90044645 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fracture of unspecified bones (PheCode 809) 121 European ancestry cases, 456,227 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044646 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Concussion (PheCode 817) 172 European ancestry cases, 456,176 European ancestry controls NA NR [11842647] (imputed) 0 concussion http://www.ebi.ac.uk/efo/EFO_0011023 GCST90044647 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Intracranial hemorrhage (injury) (PheCode 818) 509 European ancestry cases, 455,839 European ancestry controls NA NR [11842647] (imputed) 0 intracranial hemorrhage http://www.ebi.ac.uk/efo/EFO_0000551 GCST90044648 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Skull and face fracture and other intercranial injury (PheCode 819) 2,093 European ancestry cases, 454,255 European ancestry controls NA NR [11842647] (imputed) 0 Skull Fractures http://www.ebi.ac.uk/efo/EFO_1001425 GCST90044649 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dislocation (PheCode 830) 1,498 European ancestry cases, 454,850 European ancestry controls NA NR [11842647] (imputed) 0 dislocation http://www.ebi.ac.uk/efo/EFO_0009521 GCST90044650 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Internal derangement of knee (PheCode 835) 15,253 European ancestry cases, 441,095 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044651 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Traumatic arthropathy (PheCode 836) 490 European ancestry cases, 455,858 European ancestry controls NA NR [11842647] (imputed) 0 Arthropathy http://purl.obolibrary.org/obo/HP_0003040 GCST90044652 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Joint/ligament sprain (PheCode 840.3) 159 European ancestry cases, 456,189 European ancestry controls NA NR [11842647] (imputed) 0 sprain http://www.ebi.ac.uk/efo/EFO_0009582 GCST90044653 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sprains and strains (PheCode 840) 296 European ancestry cases, 456,052 European ancestry controls NA NR [11842647] (imputed) 0 sprain http://www.ebi.ac.uk/efo/EFO_0009582 GCST90044654 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemorrhage or hematoma complicating a procedure (PheCode 850) 2,473 European ancestry cases, 453,875 European ancestry controls NA NR [11842647] (imputed) 0 hemorrhage, complication http://purl.obolibrary.org/obo/MP_0001914, http://www.ebi.ac.uk/efo/EFO_0009518 GCST90044655 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complications of transplants and reattached limbs (PheCode 851) 110 European ancestry cases, 456,238 European ancestry controls NA NR [11842647] (imputed) 0 transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005198 GCST90044656 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complication of colostomy or enterostomy (PheCode 853) 392 European ancestry cases, 455,956 European ancestry controls NA NR [11842647] (imputed) 0 device complication http://www.ebi.ac.uk/efo/EFO_0009519 GCST90044657 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complications of cardiac/vascular device, implant, and graft (PheCode 854) 1,549 European ancestry cases, 454,799 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90044658 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mechanical complication of unspecified genitourinary device, implant, and graft (PheCode 857) 963 European ancestry cases, 455,385 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90044659 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complication of internal orthopedic device (PheCode 858) 3,628 European ancestry cases, 452,720 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90044660 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complication due to other implant and internal device (PheCode 859) 2,964 European ancestry cases, 453,384 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90044661 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wound or laceration of eye or eyelid (PheCode 870.1) 334 European ancestry cases, 456,014 European ancestry controls NA NR [11842647] (imputed) 0 eye injury http://www.ebi.ac.uk/efo/EFO_0009485 GCST90044662 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wound of ear (PheCode 870.2) 127 European ancestry cases, 456,221 European ancestry controls NA NR [11842647] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90044663 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other open wound of head and face (PheCode 870.3) 1,929 European ancestry cases, 454,419 European ancestry controls NA NR [11842647] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90044664 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wound of nose and sinus (PheCode 870.4) 120 European ancestry cases, 456,228 European ancestry controls NA NR [11842647] (imputed) 0 nose injury http://www.ebi.ac.uk/efo/EFO_0009623 GCST90044665 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wound of lip and mouth (PheCode 870.5) 223 European ancestry cases, 456,125 European ancestry controls NA NR [11842647] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90044666 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wound of neck (PheCode 870.6) 138 European ancestry cases, 456,210 European ancestry controls NA NR [11842647] (imputed) 0 neck injury http://www.ebi.ac.uk/efo/EFO_0009476 GCST90044667 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wounds of head; neck; and trunk (PheCode 870) 121 European ancestry cases, 456,227 European ancestry controls NA NR [11842647] (imputed) 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90044668 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wound of foot except toe(s) alone (PheCode 871.3) 130 European ancestry cases, 456,218 European ancestry controls NA NR [11842647] (imputed) 0 leg injury http://www.ebi.ac.uk/efo/EFO_0009508 GCST90044669 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Open wounds of extremities (PheCode 871) 2,989 European ancestry cases, 453,359 European ancestry controls NA NR [11842647] (imputed) 0 limb injury http://www.ebi.ac.uk/efo/EFO_0009509 GCST90044670 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Traumatic amputation (PheCode 872) 481 European ancestry cases, 455,867 European ancestry controls NA NR [11842647] (imputed) 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90044671 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Broken tooth (PheCode 873) 150 European ancestry cases, 456,198 European ancestry controls NA NR [11842647] (imputed) 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90044672 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complication of amputation stump (PheCode 874) 154 European ancestry cases, 456,194 European ancestry controls NA NR [11842647] (imputed) 0 complication http://www.ebi.ac.uk/efo/EFO_0009518 GCST90044673 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Accelerometer study data quality, good wear time (UKB data field 90015) 90,702 European ancestry cases, 6,441 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90044674 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Injuries to the nervous system (PheCode 907) 618 European ancestry cases, 455,730 European ancestry controls NA NR [11842647] (imputed) 0 nervous system injury http://www.ebi.ac.uk/efo/EFO_0009490 GCST90044675 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Toxic effect of venom (PheCode 913) 117 European ancestry cases, 456,231 European ancestry controls NA NR [11842647] (imputed) 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90044676 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Superficial injury without mention of infection (PheCode 915) 2,635 European ancestry cases, 453,713 European ancestry controls NA NR [11842647] (imputed) 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90044677 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Contusion (PheCode 916) 610 European ancestry cases, 455,738 European ancestry controls NA NR [11842647] (imputed) 0 Bruising susceptibility http://purl.obolibrary.org/obo/HP_0000978 GCST90044678 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Allergic reaction to food (PheCode 930) 160 European ancestry cases, 456,188 European ancestry controls NA NR [11842647] (imputed) 0 food allergy http://www.ebi.ac.uk/efo/EFO_1001890 GCST90044679 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic dermatitis due to solar radiation (PheCode 938.2) 174 European ancestry cases, 456,174 European ancestry controls NA NR [11842647] (imputed) 0 photosensitivity disease http://www.ebi.ac.uk/efo/EFO_1000752 GCST90044680 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Atopic/contact dermatitis due to other or unspecified (PheCode 939) 642 European ancestry cases, 455,706 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044681 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anaphylactic shock, not otherwise specified (PheCode 946) 470 European ancestry cases, 455,878 European ancestry controls NA NR [11842647] (imputed) 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90044682 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Urticaria (PheCode 947) 379 European ancestry cases, 455,969 European ancestry controls NA NR [11842647] (imputed) 0 urticaria http://www.ebi.ac.uk/efo/EFO_0005531 GCST90044683 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Allergies, other (PheCode 949) 342 European ancestry cases, 456,006 European ancestry controls NA NR [11842647] (imputed) 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90044684 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Certain early complications of trauma or procedure (PheCode 958) 259 European ancestry cases, 456,089 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90044685 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Salicylates causing adverse effects in therapeutic use (PheCode 965.3) 128 European ancestry cases, 456,220 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0009658, http://purl.obolibrary.org/obo/GO_0009410 GCST90044686 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Poisoning by analgesics, antipyretics, and antirheumatics (PheCode 965) 1,419 European ancestry cases, 454,929 European ancestry controls NA NR [11842647] (imputed) 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90044687 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Poisoning by anticonvulsants and anti-Parkinsonism drugs (PheCode 966) 330 European ancestry cases, 456,018 European ancestry controls NA NR [11842647] (imputed) 0 poisoning, response to anticonvulsant http://www.ebi.ac.uk/efo/EFO_0008546, http://purl.obolibrary.org/obo/GO_0036277 GCST90044688 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Poisoning by psychotropic agents (PheCode 969) 1,529 European ancestry cases, 454,819 European ancestry controls NA NR [11842647] (imputed) 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90044689 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Poisoning by agents primarily affecting the cardiovascular system (PheCode 972) 110 European ancestry cases, 456,238 European ancestry controls NA NR [11842647] (imputed) 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90044690 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Adverse drug events and drug allergies (PheCode 979) 285 European ancestry cases, 456,063 European ancestry controls NA NR [11842647] (imputed) 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90044691 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sepsis (PheCode 994.2) 1,573 European ancestry cases, 454,775 European ancestry controls NA NR [11842647] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90044692 Genome-wide genotyping array 2022-05-27 35512355 Jung S 2022-05-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35512355 Identification of shared loci associated with both Crohn's disease and leprosy in east Asians. Crohn's disease 1,621 Korean ancestry cases, 4,419 Korean ancestry controls 738 Korean ancestry cases, 488 Korean ancestry controls NR [5885674] (imputed) 5 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90103738 Genome-wide genotyping array 2022-05-27 35512355 Jung S 2022-05-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35512355 Identification of shared loci associated with both Crohn's disease and leprosy in east Asians. Crohn's disease or Leprosy 3,739 Chinese, Korean ancestry cases, 7,241 Chinese, Korean ancestry controls NA NR [5464908] (imputed) 2 leprosy, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0001054, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90103739 Genome-wide genotyping array 2022-05-27 35512355 Jung S 2022-05-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35512355 Identification of shared loci associated with both Crohn's disease and leprosy in east Asians. Crohn's disease or Leprosy (opposite effect) 3,739 Chinese, Korean ancestry cases, 7,241 Chinese, Korean ancestry controls NA NR [5464908] (imputed) 9 leprosy, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0001054, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90103740 Genome-wide genotyping array 2022-05-27 35512355 Jung S 2022-05-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35512355 Identification of shared loci associated with both Crohn's disease and leprosy in east Asians. Leprosy 2,118 Chinese ancestry cases, 2,822 Chinese ancestry controls 842 Chinese ancestry cases, 925 Chinese ancestry controls NR [NR] (imputed) 8 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST90103799 Genome-wide genotyping array 2022-03-25 34270706 Lin E 2021-07-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34270706 Genome-wide association study in the Taiwan biobank identifies four novel genes for human height: NABP2, RASA2, RNF41 and SLC39A5. Height 14,571 Taiwanese Han Chinese ancestry individuals 20,506 Taiwanese Han Chinese ancestry individuals Affymetrix [5682219] (imputed) 31 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90090967 Genome-wide genotyping array 2021-12-07 34720862 Ye Z 2021-10-14 Front Neurosci www.ncbi.nlm.nih.gov/pubmed/34720862 White Matter Integrity and Nicotine Dependence: Evaluating Vertical and Horizontal Pleiotropy. Smoking behavior 47,640 European ancestry cases, 246,119 European ancestry controls NA Affymetrix [NR] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90090975 Genome-wide genotyping array 2021-12-07 34720862 Ye Z 2021-10-14 Front Neurosci www.ncbi.nlm.nih.gov/pubmed/34720862 White Matter Integrity and Nicotine Dependence: Evaluating Vertical and Horizontal Pleiotropy. Smoking behaviour (cigarettes smoked per day) 142,202 European ancestry individuals NA Affymetrix [NR] 0 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90090976 Genome-wide genotyping array 2022-03-28 35245370 Roselli C 2022-03-04 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/35245370 Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse. Mitral valve prolapse 4,884 European ancestry cases, 434,649 European ancestry controls NA NR [NR] (imputed) 14 Mitral valve prolapse http://purl.obolibrary.org/obo/HP_0001634 GCST90096803 Genome-wide genotyping array 2022-03-28 35245370 Roselli C 2022-03-04 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/35245370 Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse. Mitral valve prolapse after mitral valve surgery 1,903 European ancestry cases, 428,916 European ancestry controls NA NR [NR] (imputed) 7 Mitral valve prolapse, response to surgery http://purl.obolibrary.org/obo/HP_0001634, http://www.ebi.ac.uk/efo/EFO_0009951 GCST90096804 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - carbocisteine (UKB data field 20003_1140862944) 232 European ancestry cases, 456,044 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041982 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mucodyne 375mg capsule (UKB data field 20003_1140862952) 152 European ancestry cases, 456,124 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041983 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zopiclone (UKB data field 20003_1140863144) 1,579 European ancestry cases, 454,697 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041984 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - diazepam (UKB data field 20003_1140863152) 1,247 European ancestry cases, 455,029 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041985 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nitrazepam (UKB data field 20003_1140863182) 278 European ancestry cases, 455,998 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041986 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - temazepam (UKB data field 20003_1140863202) 927 European ancestry cases, 455,349 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041987 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lorazepam (UKB data field 20003_1140863302) 157 European ancestry cases, 456,119 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041988 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - kapake tablet (UKB data field 20003_1140864070) 113 European ancestry cases, 456,163 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041989 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dovonex 50micrograms/g cream (UKB data field 20003_1140864184) 254 European ancestry cases, 456,022 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041990 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - climagest 1mg tablet (UKB data field 20003_1140864196) 247 European ancestry cases, 247,261 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041991 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - flixotide 25micrograms inhaler (UKB data field 20003_1140864286) 748 European ancestry cases, 455,528 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041992 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - xatral 2.5mg tablet (UKB data field 20003_1140864472) 157 European ancestry cases, 208,611 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041993 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - combivent inhaler (UKB data field 20003_1140864734) 190 European ancestry cases, 456,086 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041994 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lansoprazole (UKB data field 20003_1140864752) 16,241 European ancestry cases, 440,035 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041995 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bisoprolol fumarate+hydrochlorothiazide 10mg/6.25mg tablet (UKB data field 20003_1140864950) 280 European ancestry cases, 455,996 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041996 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lisinopril+hydrochlorothiazide 10mg/12.5mg tablet (UKB data field 20003_1140864952) 145 European ancestry cases, 456,131 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041997 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tramadol (UKB data field 20003_1140864992) 5,058 European ancestry cases, 451,218 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041998 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zydol 50mg capsule (UKB data field 20003_1140865000) 122 European ancestry cases, 456,154 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041999 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - viscotears liquid eye gel (UKB data field 20003_1140865010) 1,024 European ancestry cases, 455,252 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042000 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zolpidem (UKB data field 20003_1140865016) 304 European ancestry cases, 455,972 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042001 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - spasmonal 60mg capsule (UKB data field 20003_1140865336) 297 European ancestry cases, 455,979 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042002 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fybogel mebeverine sachet (UKB data field 20003_1140865350) 653 European ancestry cases, 455,623 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042003 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - gaviscon liquid (UKB data field 20003_1140865354) 2,422 European ancestry cases, 453,854 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042004 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - merbentyl 10mg tablet (UKB data field 20003_1140865382) 132 European ancestry cases, 456,144 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042005 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hyoscine butylbromide (UKB data field 20003_1140865394) 120 European ancestry cases, 456,156 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042006 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type 2 diabetes with ketoacidosis (PheCode 250.21) 86 European ancestry cases, 456,262 European ancestry controls NA NR [11842647] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90043636 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type 2 diabetes with ophthalmic manifestations (PheCode 250.23) 455 European ancestry cases, 455,893 European ancestry controls NA NR [11842647] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90043637 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type 2 diabetes (PheCode 250.2) 714 European ancestry cases, 455,634 European ancestry controls NA NR [11842647] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90043638 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other abnormal glucose (PheCode 250.42) 172 European ancestry cases, 456,176 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal glucose homeostasis http://purl.obolibrary.org/obo/HP_0011014 GCST90043639 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diabetic retinopathy (PheCode 250.7) 308 European ancestry cases, 456,040 European ancestry controls NA NR [11842647] (imputed) 0 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST90043640 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypoglycemia (PheCode 251.1) 519 European ancestry cases, 455,829 European ancestry controls NA NR [11842647] (imputed) 0 Hypoglycemic coma http://purl.obolibrary.org/obo/HP_0001325 GCST90043641 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hyperparathyroidism (PheCode 252.1) 438 European ancestry cases, 455,910 European ancestry controls NA NR [11842647] (imputed) 0 hyperparathyroidism http://www.ebi.ac.uk/efo/EFO_0008506 GCST90043642 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pituitary hypofunction (PheCode 253.2) 161 European ancestry cases, 456,187 European ancestry controls NA NR [11842647] (imputed) 0 hypopituitarism http://www.ebi.ac.uk/efo/EFO_0001380 GCST90043643 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Glucocorticoid deficiency (PheCode 255.21) 226 European ancestry cases, 456,122 European ancestry controls NA NR [11842647] (imputed) 0 adrenocortical insufficiency http://www.ebi.ac.uk/efo/EFO_0009491 GCST90043644 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral deficiency NEC (PheCode 262) 120 European ancestry cases, 456,228 European ancestry controls NA NR [11842647] (imputed) 0 nutritional deficiency disease http://www.ebi.ac.uk/efo/EFO_1001067 GCST90043645 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Light smokers - at least 100 smokes in lifetime (UKB data field 2644) 56,073 European ancestry cases, 65,972 European ancestry controls NA NR [11842647] (imputed) 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90043646 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-butter spread type details: Flora Pro-Active or Benecol (UKB data field 2654_2) 36,208 European ancestry cases, 202,395 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90043647 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-butter spread type details: Soft (tub) margarine (UKB data field 2654_4) 29,965 European ancestry cases, 208,638 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90043648 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-butter spread type details: Hard (block) margarine (UKB data field 2654_5) 307 European ancestry cases, 238,296 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90043649 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-butter spread type details: Olive oil based spread (eg: Bertolli) (UKB data field 2654_6) 58,872 European ancestry cases, 179,731 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90043650 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-butter spread type details: Polyunsaturated/sunflower oil based spread (eg: Flora) (UKB data field 2654_7) 80,621 European ancestry cases, 157,982 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90043651 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-butter spread type details: Other low or reduced fat spread (UKB data field 2654_8) 23,957 European ancestry cases, 214,646 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90043652 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Non-butter spread type details: Other type of spread/margarine (UKB data field 2654_9) 8,673 European ancestry cases, 229,930 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90043653 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for reducing amount of alcohol drunk: Illness or ill health (UKB data field 2664_1) 12,143 European ancestry cases, 157,687 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043654 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for reducing amount of alcohol drunk: Doctor's advice (UKB data field 2664_2) 3,808 European ancestry cases, 166,022 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043655 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - voltarol 25mg e/c tablet (UKB data field 20003_1140871168) 502 European ancestry cases, 455,774 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042096 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - etodolac (UKB data field 20003_1140871188) 328 European ancestry cases, 455,948 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042097 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lodine 200mg tablet (UKB data field 20003_1140871196) 203 European ancestry cases, 456,073 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042098 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - arthrotec tablet (UKB data field 20003_1140871266) 645 European ancestry cases, 455,631 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042099 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ibuprofen (UKB data field 20003_1140871310) 56,815 European ancestry cases, 399,461 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042100 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of thyroid (PheCode 246) 124 European ancestry cases, 456,224 European ancestry controls NA NR [11842647] (imputed) 0 thyroid disease http://www.ebi.ac.uk/efo/EFO_1000627 GCST90043630 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other serious medical condition/disability diagnosed by doctor (UKB data field 2473) 92,032 European ancestry cases, 355,746 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043631 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Taking other prescription medications (UKB data field 2492) 213,640 European ancestry cases, 241,153 European ancestry controls NA NR [11842647] (imputed) 0 number of treatments or medications taken, self-reported http://www.ebi.ac.uk/efo/EFO_0009803 GCST90043632 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type 1 diabetes with ketoacidosis (PheCode 250.11) 228 European ancestry cases, 456,120 European ancestry controls NA NR [11842647] (imputed) 0 diabetic ketoacidosis, type 1 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_1000897, http://purl.obolibrary.org/obo/MONDO_0005147 GCST90043633 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type 1 diabetes with ophthalmic manifestations (PheCode 250.13) 213 European ancestry cases, 456,135 European ancestry controls NA NR [11842647] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90043634 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type 1 diabetes (PheCode 250.1) 367 European ancestry cases, 455,981 European ancestry controls NA NR [11842647] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90043635 Genome-wide genotyping array 2022-03-22 34859065 Zhang F 2021-11-11 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/34859065 Shared Genetic Liability and Causal Associations Between Major Depressive Disorder and Cardiovascular Diseases. Major depressive disorder or stroke (pleiotropy) 135,458 European ancestry MDD cases, 40,585 European ancestry stroke cases, 751,012 European ancestry controls NA NR [8243736] 13 stroke, major depressive disorder http://www.ebi.ac.uk/efo/EFO_0000712, http://purl.obolibrary.org/obo/MONDO_0002009 GCST90095484 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - indomethacin (UKB data field 20003_1140871336) 280 European ancestry cases, 455,996 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042101 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - naproxen (UKB data field 20003_1140871462) 2,899 European ancestry cases, 453,377 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042102 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - naprosyn 250mg tablet (UKB data field 20003_1140871472) 313 European ancestry cases, 455,963 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042103 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ketoprofen (UKB data field 20003_1140871506) 132 European ancestry cases, 456,144 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042104 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mefenamic acid (UKB data field 20003_1140871542) 479 European ancestry cases, 455,797 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042105 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - piroxicam (UKB data field 20003_1140871666) 156 European ancestry cases, 456,120 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042106 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tylex capsule (UKB data field 20003_1140871680) 211 European ancestry cases, 456,065 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042107 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - solpadol caplet (UKB data field 20003_1140871688) 347 European ancestry cases, 455,929 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042108 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - morphine (UKB data field 20003_1140871692) 260 European ancestry cases, 456,016 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042109 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - buprenorphine (UKB data field 20003_1140871732) 294 European ancestry cases, 455,982 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042110 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dixarit 25mcg tablet (UKB data field 20003_1140871984) 108 European ancestry cases, 247,400 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042111 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - paramax tablet (UKB data field 20003_1140872036) 152 European ancestry cases, 456,124 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042112 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - migril tablet (UKB data field 20003_1140872058) 108 European ancestry cases, 456,168 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042113 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tegretol 100mg tablet (UKB data field 20003_1140872072) 999 European ancestry cases, 455,277 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042114 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - epanutin 25mg capsule (UKB data field 20003_1140872112) 321 European ancestry cases, 455,955 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042115 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clonazepam (UKB data field 20003_1140872150) 322 European ancestry cases, 455,954 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042116 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sodium valproate (UKB data field 20003_1140872198) 433 European ancestry cases, 455,843 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042117 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - epilim 100mg crushable tablet (UKB data field 20003_1140872200) 750 European ancestry cases, 455,526 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042118 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - gabapentin (UKB data field 20003_1140872228) 2,113 European ancestry cases, 454,163 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042119 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lamotrigine (UKB data field 20003_1140872290) 550 European ancestry cases, 455,726 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042120 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - madopar 62.5 capsule (UKB data field 20003_1140872338) 121 European ancestry cases, 456,155 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042121 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nicotine product (UKB data field 20003_1140872492) 176 European ancestry cases, 456,100 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042122 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - phenoxymethylpenicillin (UKB data field 20003_1140872590) 103 European ancestry cases, 456,173 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042123 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - flucloxacillin (UKB data field 20003_1140872694) 157 European ancestry cases, 456,119 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042124 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - doxycycline (UKB data field 20003_1140873394) 423 European ancestry cases, 455,853 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042125 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - colchicine (UKB data field 20003_1140875486) 224 European ancestry cases, 456,052 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042151 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - movelat gel (UKB data field 20003_1140875632) 156 European ancestry cases, 456,120 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042152 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - timolol 0.25% eye drops (UKB data field 20003_1140875840) 322 European ancestry cases, 455,954 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042153 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hypromellose (UKB data field 20003_1140875990) 775 European ancestry cases, 455,501 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042154 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - flixonase 50micrograms aqueous nasal spray (UKB data field 20003_1140876076) 1,803 European ancestry cases, 454,473 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042155 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - beconase 50micrograms nasal spray (UKB data field 20003_1140876136) 2,996 European ancestry cases, 453,280 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042156 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rhinocort 50micrograms nasal spray (UKB data field 20003_1140876146) 171 European ancestry cases, 456,105 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042157 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - aqueous cream bp (UKB data field 20003_1140876404) 395 European ancestry cases, 455,881 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042158 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - multivitamin+mineral preparations (UKB data field 20003_1140876592) 6,245 European ancestry cases, 450,031 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042159 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcium+ergocalciferol tablet (UKB data field 20003_1140877630) 198 European ancestry cases, 456,078 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042160 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sodium bicarbonate (UKB data field 20003_1140877826) 116 European ancestry cases, 456,160 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042161 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - voltarol emulgel (UKB data field 20003_1140877892) 252 European ancestry cases, 456,024 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042162 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - diclofenac sodium+misoprostol (UKB data field 20003_1140878036) 309 European ancestry cases, 455,967 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042163 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tears naturale eye drops (UKB data field 20003_1140878172) 128 European ancestry cases, 456,148 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042164 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sno-tears eye drops (UKB data field 20003_1140878184) 101 European ancestry cases, 456,175 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042165 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - liquifilm tears 1.4% eye drops (UKB data field 20003_1140878186) 177 European ancestry cases, 456,099 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042166 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - diprobase cream (UKB data field 20003_1140878226) 732 European ancestry cases, 455,544 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042167 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - e45 cream (UKB data field 20003_1140878304) 315 European ancestry cases, 455,961 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042168 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oilatum cream (UKB data field 20003_1140878324) 175 European ancestry cases, 456,101 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042169 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - capasal shampoo (UKB data field 20003_1140878512) 109 European ancestry cases, 456,167 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042170 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - canesten 1% cream (UKB data field 20003_1140878530) 119 European ancestry cases, 456,157 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042171 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - manevac granules (UKB data field 20003_1140879392) 155 European ancestry cases, 456,121 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042172 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - docusate sodium (UKB data field 20003_1140879404) 373 European ancestry cases, 455,903 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042173 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ranitidine (UKB data field 20003_1140879406) 7,554 European ancestry cases, 448,722 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042174 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - alverine (UKB data field 20003_1140879424) 270 European ancestry cases, 456,006 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042175 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tetracycline (UKB data field 20003_1140873450) 125 European ancestry cases, 456,151 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042126 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lymecycline (UKB data field 20003_1140873474) 216 European ancestry cases, 456,060 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042127 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tetralysal 300 capsule (UKB data field 20003_1140873476) 175 European ancestry cases, 456,101 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042128 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - minocycline (UKB data field 20003_1140873480) 193 European ancestry cases, 456,083 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042129 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oxytetracycline (UKB data field 20003_1140873548) 1,340 European ancestry cases, 454,936 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042130 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - erythromycin (UKB data field 20003_1140873608) 341 European ancestry cases, 455,935 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042131 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - azithromycin (UKB data field 20003_1140873642) 118 European ancestry cases, 456,158 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042132 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - trimethoprim (UKB data field 20003_1140873966) 452 European ancestry cases, 455,824 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042133 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - metronidazole (UKB data field 20003_1140874014) 160 European ancestry cases, 456,116 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042134 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nitrofurantoin (UKB data field 20003_1140874126) 259 European ancestry cases, 456,017 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042135 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ciprofloxacin (UKB data field 20003_1140874138) 165 European ancestry cases, 456,111 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042136 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - aciclovir (UKB data field 20003_1140874370) 359 European ancestry cases, 455,917 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042137 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - quinine (UKB data field 20003_1140874420) 3,057 European ancestry cases, 453,219 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042138 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - glucophage 500mg tablet (UKB data field 20003_1140874686) 398 European ancestry cases, 455,878 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042139 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - gliclazide (UKB data field 20003_1140874744) 3,782 European ancestry cases, 452,494 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042140 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - betamethasone (UKB data field 20003_1140874790) 695 European ancestry cases, 455,581 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042141 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dexamethasone (UKB data field 20003_1140874816) 107 European ancestry cases, 456,169 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042142 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - thyroxine sodium (UKB data field 20003_1140874852) 1,247 European ancestry cases, 455,029 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042143 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - carbimazole (UKB data field 20003_1140874866) 369 European ancestry cases, 455,907 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042144 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hydrocortisone (UKB data field 20003_1140874896) 816 European ancestry cases, 455,460 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042145 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - prednisolone (UKB data field 20003_1140874930) 2,595 European ancestry cases, 453,681 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042146 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nabumetone (UKB data field 20003_1140875336) 204 European ancestry cases, 456,072 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042147 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - plaquenil 200mg tablet (UKB data field 20003_1140875392) 193 European ancestry cases, 456,083 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042148 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - allopurinol (UKB data field 20003_1140875408) 5,161 European ancestry cases, 451,115 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042149 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - baclofen (UKB data field 20003_1140875420) 496 European ancestry cases, 455,780 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042150 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D06.1: Carcinoma in situ of exocervix 387 European ancestry cases, 247,153 European ancestry controls NA NR [11842647] (imputed) 0 uterine cervix carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0042487 GCST90043929 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D06.9: Carcinoma in situ of cervix, unspecified 3,145 European ancestry cases, 244,395 European ancestry controls NA NR [11842647] (imputed) 0 uterine cervix carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0042487 GCST90043930 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D07.1: Carcinoma in situ of vulva 113 European ancestry cases, 247,427 European ancestry controls NA NR [11842647] (imputed) 0 vulvar carcinoma http://www.ebi.ac.uk/efo/EFO_0002921 GCST90043931 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D07.5: Carcinoma in situ of prostate 349 European ancestry cases, 208,459 European ancestry controls NA NR [11842647] (imputed) 0 Grade III Prostatic Intraepithelial Neoplasia http://www.ebi.ac.uk/efo/EFO_1000283 GCST90043932 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D09.0: Carcinoma in situ of bladder 614 European ancestry cases, 455,734 European ancestry controls NA NR [11842647] (imputed) 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90043933 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D32.0: Benign neoplasm of cerebral meninges 307 European ancestry cases, 456,041 European ancestry controls NA NR [11842647] (imputed) 0 meningeal neoplasm http://www.ebi.ac.uk/efo/EFO_0003851 GCST90043934 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D33.3: Benign neoplasm of brain, supratentorial 176 European ancestry cases, 456,172 European ancestry controls NA NR [11842647] (imputed) 0 Benign Brain Neoplasm http://www.ebi.ac.uk/efo/EFO_1000107 GCST90043935 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D35.2: Benign neoplasm of pituitary gland 209 European ancestry cases, 456,139 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm of pituitary gland http://purl.obolibrary.org/obo/MONDO_0021439 GCST90043936 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D37.4: Benign neoplasm of colon 109 European ancestry cases, 456,239 European ancestry controls NA NR [11842647] (imputed) 0 benign colon neoplasm http://purl.obolibrary.org/obo/MONDO_0002278 GCST90043937 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D41.4: Neoplasm of uncertain behavior of bladder 831 European ancestry cases, 455,517 European ancestry controls NA NR [11842647] (imputed) 0 GCST90043938 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D45: Polycythaemia vera 151 European ancestry cases, 456,197 European ancestry controls NA NR [11842647] (imputed) 0 polycythemia vera http://www.ebi.ac.uk/efo/EFO_0002429 GCST90043939 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D46.9: Myelodysplastic syndrome, unspecified 105 European ancestry cases, 456,243 European ancestry controls NA NR [11842647] (imputed) 0 myelodysplastic syndrome http://www.ebi.ac.uk/efo/EFO_0000198 GCST90043940 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D47.1: Chronic myeloproliferative disease 143 European ancestry cases, 456,205 European ancestry controls NA NR [11842647] (imputed) 0 chronic myeloproliferative disorder http://www.ebi.ac.uk/efo/EFO_0002428 GCST90043941 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D47.2: Monoclonal gammopathy of undetermined significance 110 European ancestry cases, 456,238 European ancestry controls NA NR [11842647] (imputed) 0 monoclonal gammopathy http://www.ebi.ac.uk/efo/EFO_0000203 GCST90043942 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behaviour of cancer tumour: benign, PHESANT recoding (UKB data field 40012_0) 1,098 European ancestry cases, 455,250 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90043943 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behaviour of cancer tumour: uncertain whether benign or malignant, PHESANT recoding (UKB data field 40012_1) 2,826 European ancestry cases, 453,522 European ancestry controls NA NR [11842647] (imputed) 0 GCST90043944 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behaviour of cancer tumour: carcinoma in situ, PHESANT recoding (UKB data field 40012_2) 12,081 European ancestry cases, 444,267 European ancestry controls NA NR [11842647] (imputed) 0 in situ carcinoma http://purl.obolibrary.org/obo/MONDO_0004647 GCST90043945 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behaviour of cancer tumour: malignant, primary site, PHESANT recoding (UKB data field 40012_3) 60,858 European ancestry cases, 395,490 European ancestry controls NA NR [11842647] (imputed) 1 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90043946 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behaviour of cancer tumour: malignant, microinvasive, PHESANT recoding (UKB data field 40012_5) 181 European ancestry cases, 456,167 European ancestry controls NA NR [11842647] (imputed) 0 metastatic malignant neoplasm http://purl.obolibrary.org/obo/MONDO_0024880 GCST90043947 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behaviour of cancer tumour: malignant, metastatic site, PHESANT recoding (UKB data field 40012_6) 395 European ancestry cases, 455,953 European ancestry controls NA NR [11842647] (imputed) 0 metastatic malignant neoplasm http://purl.obolibrary.org/obo/MONDO_0024880 GCST90043948 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Essential hypertension (PheCode 401.1) 1,105 European ancestry cases, 455,243 European ancestry controls NA NR [11842647] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90043949 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypertensive chronic kidney disease (PheCode 401.22) 365 European ancestry cases, 455,983 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043950 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gestational diabetes only (UKB data field 4041) 864 European ancestry cases, 6,977 European ancestry controls NA NR [11842647] (imputed) 0 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST90043951 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Facial pains for three months (UKB data field 4067) 4,005 European ancestry cases, 4,369 European ancestry controls NA NR [11842647] (imputed) 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90043952 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Unstable angina (intermediate coronary syndrome) (PheCode 411.1) 4,403 European ancestry cases, 451,945 European ancestry controls NA NR [11842647] (imputed) 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90043953 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C81.1: Nodular sclerosis classical Hodgkin lymphoma 126 European ancestry cases, 456,222 European ancestry controls NA NR [11842647] (imputed) 0 nodular sclerosis Hodgkin lymphoma http://www.ebi.ac.uk/efo/EFO_0004708 GCST90043904 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C82.9: Follicular lymphoma, unspecified 298 European ancestry cases, 456,050 European ancestry controls NA NR [11842647] (imputed) 0 follicular lymphoma http://purl.obolibrary.org/obo/MONDO_0018906 GCST90043905 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C83.3: Diffuse large B-cell lymphoma 616 European ancestry cases, 455,732 European ancestry controls NA NR [11842647] (imputed) 0 diffuse large B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000403 GCST90043906 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C83.8: Other non-follicular lymphoma 127 European ancestry cases, 456,221 European ancestry controls NA NR [11842647] (imputed) 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90043907 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C85.7: Other specified types of non-Hodgkin lymphoma 112 European ancestry cases, 456,236 European ancestry controls NA NR [11842647] (imputed) 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90043908 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C85.9: Non-Hodgkin lymphoma, unspecified 292 European ancestry cases, 456,056 European ancestry controls NA NR [11842647] (imputed) 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90043909 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C90.0: Multiple myeloma 488 European ancestry cases, 455,860 European ancestry controls NA NR [11842647] (imputed) 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90043910 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C91.1: Chronic lymphocytic leukemia of B-cell type 517 European ancestry cases, 455,831 European ancestry controls NA NR [11842647] (imputed) 0 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90043911 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C92.0: Acute myeloblastic leukaemia 220 European ancestry cases, 456,128 European ancestry controls NA NR [11842647] (imputed) 0 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST90043912 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C92.1: Chronic myeloid leukaemia, BCR/ABL-positive 110 European ancestry cases, 456,238 European ancestry controls NA NR [11842647] (imputed) 0 chronic myelogenous leukemia http://www.ebi.ac.uk/efo/EFO_0000339 GCST90043913 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D01.0: Carcinoma in situ of colon 138 European ancestry cases, 456,210 European ancestry controls NA NR [11842647] (imputed) 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90043914 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D01.2: Carcinoma in situ of anus 107 European ancestry cases, 456,241 European ancestry controls NA NR [11842647] (imputed) 0 anal carcinoma http://purl.obolibrary.org/obo/MONDO_0003199 GCST90043915 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D03.3: Melanoma in situ of other and unspecified parts of face 361 European ancestry cases, 455,987 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043916 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D03.5: Melanoma in situ of trunk 252 European ancestry cases, 456,096 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043917 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D03.6: Melanoma in situ of upper limb, including shoulder 258 European ancestry cases, 456,090 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043918 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D03.7: Melanoma in situ of lower limb, including hip 249 European ancestry cases, 456,099 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043919 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D04.3: Carcinoma in situ of skin of other and unspecified parts of face 277 European ancestry cases, 456,071 European ancestry controls NA NR [11842647] (imputed) 0 skin carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0004641 GCST90043920 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D04.5: Carcinoma in situ of skin of trunk 180 European ancestry cases, 456,168 European ancestry controls NA NR [11842647] (imputed) 0 skin carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0004641 GCST90043921 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D04.6: Carcinoma in situ of skin of upper limb, including shoulder 218 European ancestry cases, 456,130 European ancestry controls NA NR [11842647] (imputed) 0 skin carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0004641 GCST90043922 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D04.7: Carcinoma in situ of skin of lower limb, including hip 430 European ancestry cases, 455,918 European ancestry controls NA NR [11842647] (imputed) 1 skin carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0004641 GCST90043923 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D04.9: Carcinoma in situ of skin, unspecified 128 European ancestry cases, 456,220 European ancestry controls NA NR [11842647] (imputed) 0 skin carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0004641 GCST90043924 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D05.0: Lobular carcinoma in situ of breast 184 European ancestry cases, 247,356 European ancestry controls NA NR [11842647] (imputed) 0 Lobular Breast Carcinoma In Situ http://www.ebi.ac.uk/efo/EFO_1000326 GCST90043925 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D05.1: Intraductal carcinoma in situ of breast 1,895 European ancestry cases, 454,453 European ancestry controls NA NR [11842647] (imputed) 0 intraductal breast neoplasm http://purl.obolibrary.org/obo/MONDO_0002488 GCST90043926 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D05.7: Other carcinoma in situ of breast 144 European ancestry cases, 247,396 European ancestry controls NA NR [11842647] (imputed) 0 breast carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0004658 GCST90043927 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 D05.9: Unspecified type of carcinoma in situ of breast 213 European ancestry cases, 247,327 European ancestry controls NA NR [11842647] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90043928 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.8: Overlapping lesion of skin 141 European ancestry cases, 456,207 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043879 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.9: Malignant neoplasm of skin, unspecified 4,407 European ancestry cases, 451,941 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043880 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C45.0: Mesothelioma of pleura 210 European ancestry cases, 456,138 European ancestry controls NA NR [11842647] (imputed) 0 Pleural Mesothelioma http://www.ebi.ac.uk/efo/EFO_1000485 GCST90043881 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C49.2: Malignant neoplasm of connective and soft tissue of lower limb, including hip 108 European ancestry cases, 456,240 European ancestry controls NA NR [11842647] (imputed) 0 connective and soft tissue neoplasm http://purl.obolibrary.org/obo/MONDO_0044334 GCST90043882 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C50.1: Malignant neoplasm of central portion of breast 440 European ancestry cases, 455,908 European ancestry controls NA NR [11842647] (imputed) 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90043883 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C50.2: Malignant neoplasm of upper-inner quadrant of breast 975 European ancestry cases, 246,565 European ancestry controls NA NR [11842647] (imputed) 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90043884 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C50.3: Malignant neoplasm of lower-inner quadrant of breast 523 European ancestry cases, 455,825 European ancestry controls NA NR [11842647] (imputed) 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90043885 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C50.4: Malignant neoplasm of upper-outer quadrant of breast 3,305 European ancestry cases, 244,235 European ancestry controls NA NR [11842647] (imputed) 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90043886 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C50.5: Malignant neoplasm of lower-outer quadrant of breast 617 European ancestry cases, 246,923 European ancestry controls NA NR [11842647] (imputed) 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90043887 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C50.8: Malignant neoplasm of overlapping sites of breast 858 European ancestry cases, 246,682 European ancestry controls NA NR [11842647] (imputed) 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90043888 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C50.9: Malignant neoplasm of breast of unspecified site 6,087 European ancestry cases, 450,261 European ancestry controls NA NR [11842647] (imputed) 1 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90043889 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C51.9: Malignant neoplasm of vulva, unspecified 104 European ancestry cases, 247,436 European ancestry controls NA NR [11842647] (imputed) 0 vulvar neoplasm http://purl.obolibrary.org/obo/MONDO_0021049 GCST90043890 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C53.9: Malignant neoplasm of cervix uteri, unspecified 372 European ancestry cases, 247,168 European ancestry controls NA NR [11842647] (imputed) 0 uterine cervix neoplasm http://purl.obolibrary.org/obo/MONDO_0021230 GCST90043891 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C54.1: Malignant neoplasm of endometrium 1,477 European ancestry cases, 246,063 European ancestry controls NA NR [11842647] (imputed) 0 endometrial cancer http://purl.obolibrary.org/obo/MONDO_0011962 GCST90043892 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C56: Malignant neoplasm of ovary 1,079 European ancestry cases, 246,461 European ancestry controls NA NR [11842647] (imputed) 0 ovarian neoplasm http://www.ebi.ac.uk/efo/EFO_0003893 GCST90043893 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C61: Malignant neoplasm of prostate 7,769 European ancestry cases, 201,039 European ancestry controls NA NR [11842647] (imputed) 2 prostate cancer http://purl.obolibrary.org/obo/MONDO_0008315 GCST90043894 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C62.1: Malignant neoplasm of descended testis 103 European ancestry cases, 208,705 European ancestry controls NA NR [11842647] (imputed) 0 testicular neoplasm http://www.ebi.ac.uk/efo/EFO_0004281 GCST90043895 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C62.9: Malignant neoplasm of testis, unspecified 426 European ancestry cases, 208,382 European ancestry controls NA NR [11842647] (imputed) 0 testicular neoplasm http://www.ebi.ac.uk/efo/EFO_0004281 GCST90043896 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C64: Malignant neoplasm of kidney, except renal pelvis 1,103 European ancestry cases, 455,245 European ancestry controls NA NR [11842647] (imputed) 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90043897 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C67.9: Malignant neoplasm of bladder, unspecified 945 European ancestry cases, 455,403 European ancestry controls NA NR [11842647] (imputed) 0 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90043898 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C71.1: Malignant neoplasm of brain, frontal lobe 134 European ancestry cases, 456,214 European ancestry controls NA NR [11842647] (imputed) 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90043899 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C71.2: Malignant neoplasm of brain, temporal lobe 112 European ancestry cases, 456,236 European ancestry controls NA NR [11842647] (imputed) 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90043900 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C71.9: Malignant neoplasm of brain, unspecified 110 European ancestry cases, 456,238 European ancestry controls NA NR [11842647] (imputed) 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90043901 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C73: Malignant neoplasm of thyroid gland 506 European ancestry cases, 455,842 European ancestry controls NA NR [11842647] (imputed) 0 thyroid cancer http://purl.obolibrary.org/obo/MONDO_0002108 GCST90043902 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C80: Malignant neoplasm without specification of site 182 European ancestry cases, 456,166 European ancestry controls NA NR [11842647] (imputed) 0 GCST90043903 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of middle ear and mastoid (PheCode 385) 118 European ancestry cases, 456,230 European ancestry controls NA NR [11842647] (imputed) 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90043829 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Meniere's disease (PheCode 386.1) 171 European ancestry cases, 456,177 European ancestry controls NA NR [11842647] (imputed) 0 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90043830 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peripheral or central vertigo (PheCode 386.2) 284 European ancestry cases, 456,064 European ancestry controls NA NR [11842647] (imputed) 0 peripheral vertigo, central nervous system origin vertigo http://purl.obolibrary.org/obo/MONDO_0004900, http://purl.obolibrary.org/obo/MONDO_0002317 GCST90043831 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Labyrinthitis (PheCode 386.3) 699 European ancestry cases, 455,649 European ancestry controls NA NR [11842647] (imputed) 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90043832 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dizziness and giddiness (Light-headedness and vertigo) (PheCode 386.9) 2,251 European ancestry cases, 454,097 European ancestry controls NA NR [11842647] (imputed) 0 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90043833 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sensorineural hearing loss (PheCode 389.1) 129 European ancestry cases, 456,219 European ancestry controls NA NR [11842647] (imputed) 0 sensorineural hearing loss http://www.ebi.ac.uk/efo/EFO_1001176 GCST90043834 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Conductive hearing loss (PheCode 389.2) 210 European ancestry cases, 456,138 European ancestry controls NA NR [11842647] (imputed) 0 Conductive hearing impairment http://purl.obolibrary.org/obo/HP_0000405 GCST90043835 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hearing loss (PheCode 389) 585 European ancestry cases, 455,763 European ancestry controls NA NR [11842647] (imputed) 0 sensorineural hearing loss http://www.ebi.ac.uk/efo/EFO_1001176 GCST90043836 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mitral valve disease (PheCode 394.2) 889 European ancestry cases, 455,459 European ancestry controls NA NR [11842647] (imputed) 0 mitral valve disease http://www.ebi.ac.uk/efo/EFO_0009557 GCST90043837 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aortic valve disease (PheCode 394.3) 557 European ancestry cases, 455,791 European ancestry controls NA NR [11842647] (imputed) 0 aortic valve disease http://www.ebi.ac.uk/efo/EFO_0009531 GCST90043838 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disease of tricuspid valve (PheCode 394.7) 135 European ancestry cases, 456,213 European ancestry controls NA NR [11842647] (imputed) 0 tricuspid valve disease http://www.ebi.ac.uk/efo/EFO_0009568 GCST90043839 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rheumatic disease of the heart valves (PheCode 394) 275 European ancestry cases, 456,073 European ancestry controls NA NR [11842647] (imputed) 0 aortic valve disease http://www.ebi.ac.uk/efo/EFO_0009531 GCST90043840 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nonrheumatic mitral valve disorders (PheCode 395.1) 820 European ancestry cases, 455,528 European ancestry controls NA NR [11842647] (imputed) 0 mitral valve disease http://www.ebi.ac.uk/efo/EFO_0009557 GCST90043841 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C01: Malignant neoplasm of base of tongue 116 European ancestry cases, 456,232 European ancestry controls NA NR [11842647] (imputed) 0 tongue neoplasm http://www.ebi.ac.uk/efo/EFO_0003871 GCST90043842 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C09.9: Malignant neoplasm of tonsil, unspecified 187 European ancestry cases, 456,161 European ancestry controls NA NR [11842647] (imputed) 0 tonsil cancer http://www.ebi.ac.uk/efo/EFO_1001214 GCST90043843 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C15.5: Malignant neoplasm of lower third of esophagus 319 European ancestry cases, 456,029 European ancestry controls NA NR [11842647] (imputed) 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90043844 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C15.9: Malignant neoplasm of esophagus, unspecified 218 European ancestry cases, 456,130 European ancestry controls NA NR [11842647] (imputed) 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90043845 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C16.0: Malignant neoplasm of cardia of stomach 192 European ancestry cases, 456,156 European ancestry controls NA NR [11842647] (imputed) 0 cardia cancer http://purl.obolibrary.org/obo/MONDO_0001063 GCST90043846 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C16.9: Malignant neoplasm of stomach, unspecified 145 European ancestry cases, 456,203 European ancestry controls NA NR [11842647] (imputed) 0 gastric cancer http://purl.obolibrary.org/obo/MONDO_0001056 GCST90043847 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.0: Malignant neoplasm of cecum 601 European ancestry cases, 455,747 European ancestry controls NA NR [11842647] (imputed) 0 cecum cancer http://purl.obolibrary.org/obo/MONDO_0002033 GCST90043848 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.2: Malignant neoplasm of ascending colon 378 European ancestry cases, 455,970 European ancestry controls NA NR [11842647] (imputed) 0 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90043849 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.3: Malignant neoplasm of hepatic flexure of colon 143 European ancestry cases, 456,205 European ancestry controls NA NR [11842647] (imputed) 0 malignant colon neoplasm http://purl.obolibrary.org/obo/MONDO_0021063 GCST90043850 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.4: Malignant neoplasm of transverse colon 227 European ancestry cases, 456,121 European ancestry controls NA NR [11842647] (imputed) 0 malignant colon neoplasm http://purl.obolibrary.org/obo/MONDO_0021063 GCST90043851 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.5: Malignant neoplasm of splenic flexure of colon 117 European ancestry cases, 456,231 European ancestry controls NA NR [11842647] (imputed) 0 malignant colon neoplasm http://purl.obolibrary.org/obo/MONDO_0021063 GCST90043852 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.6: Malignant neoplasm of descending colon 153 European ancestry cases, 456,195 European ancestry controls NA NR [11842647] (imputed) 0 malignant colon neoplasm http://purl.obolibrary.org/obo/MONDO_0021063 GCST90043853 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.7: Malignant neoplasm of sigmoid colon 1,229 European ancestry cases, 455,119 European ancestry controls NA NR [11842647] (imputed) 0 sigmoid neoplasm http://www.ebi.ac.uk/efo/EFO_1001181 GCST90043854 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C18.9: Malignant neoplasm of colon, unspecified 274 European ancestry cases, 456,074 European ancestry controls NA NR [11842647] (imputed) 0 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90043855 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C19: Malignant neoplasm of rectosigmoid junction 413 European ancestry cases, 455,935 European ancestry controls NA NR [11842647] (imputed) 0 rectosigmoid junction neoplasm http://purl.obolibrary.org/obo/MONDO_0002423 GCST90043856 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C20: Malignant neoplasm of rectum 1,473 European ancestry cases, 454,875 European ancestry controls NA NR [11842647] (imputed) 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90043857 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C22.0: Liver cell carcinoma 123 European ancestry cases, 456,225 European ancestry controls NA NR [11842647] (imputed) 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90043858 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C22.1: Intrahepatic bile duct carcinoma 104 European ancestry cases, 456,244 European ancestry controls NA NR [11842647] (imputed) 0 intrahepatic cholangiocarcinoma http://www.ebi.ac.uk/efo/EFO_1001961 GCST90043859 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C25.0: Malignant neoplasm of head of pancreas 209 European ancestry cases, 456,139 European ancestry controls NA NR [11842647] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90043860 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C25.9: Malignant neoplasm of pancreas, unspecified 232 European ancestry cases, 456,116 European ancestry controls NA NR [11842647] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90043861 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C32.0: Malignant neoplasm of glottis 175 European ancestry cases, 456,173 European ancestry controls NA NR [11842647] (imputed) 0 glottis neoplasm http://purl.obolibrary.org/obo/MONDO_0002353 GCST90043862 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C34.1: Malignant neoplasm of upper lobe, bronchus or lung 998 European ancestry cases, 455,350 European ancestry controls NA NR [11842647] (imputed) 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90043863 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C34.3: Malignant neoplasm of lower lobe, bronchus or lung 528 European ancestry cases, 455,820 European ancestry controls NA NR [11842647] (imputed) 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90043864 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C34.9: Malignant neoplasm of unspecified part of bronchus or lung 535 European ancestry cases, 455,813 European ancestry controls NA NR [11842647] (imputed) 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90043865 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C43.3: Malignant melanoma of other and unspecified parts of face 219 European ancestry cases, 456,129 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043866 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C43.5: Malignant melanoma of trunk 956 European ancestry cases, 455,392 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043867 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C43.6: Malignant melanoma of upper limb, including shoulder 769 European ancestry cases, 455,579 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043868 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C43.7: Malignant melanoma of lower limb, including hip 1,049 European ancestry cases, 455,299 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043869 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C43.9: Malignant melanoma of skin, unspecified 111 European ancestry cases, 456,237 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90043870 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.0: Other and unspecified malignant neoplasm of skin of lip 302 European ancestry cases, 456,046 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043871 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.1: Other and unspecified malignant neoplasm of skin of eyelid, including canthus 917 European ancestry cases, 455,431 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043872 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.2: Other and unspecified malignant neoplasm of skin of ear and external auricular canal 660 European ancestry cases, 455,688 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043873 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.3: Other and unspecified malignant neoplasm of skin of other and unspecified parts of face 6,046 European ancestry cases, 450,302 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043874 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.4: Other and unspecified malignant neoplasm of skin of scalp and neck 1,215 European ancestry cases, 455,133 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043875 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.5: Other and unspecified malignant neoplasm of skin of trunk 2,603 European ancestry cases, 453,745 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043876 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.6: Other and unspecified malignant neoplasm of skin of upper limb, including shoulder 1,377 European ancestry cases, 454,971 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043877 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. ICD10 C44.7: Other and unspecified malignant neoplasm of skin of lower limb, including hip 1,067 European ancestry cases, 455,281 European ancestry controls NA NR [11842647] (imputed) 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90043878 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Strabismus (not specified as paralytic) (PheCode 378.1) 866 European ancestry cases, 455,482 European ancestry controls NA NR [11842647] (imputed) 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90043804 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Paralytic strabismus (PheCode 378.5) 173 European ancestry cases, 456,175 European ancestry controls NA NR [11842647] (imputed) 0 paralytic strabismus http://www.ebi.ac.uk/efo/EFO_0009678 GCST90043805 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of vitreous body (PheCode 379.2) 610 European ancestry cases, 455,738 European ancestry controls NA NR [11842647] (imputed) 0 vitreous body disease http://www.ebi.ac.uk/efo/EFO_0008624 GCST90043806 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Aphakia and other disorders of lens (PheCode 379.3) 1,859 European ancestry cases, 454,489 European ancestry controls NA NR [11842647] (imputed) 0 lens disease http://www.ebi.ac.uk/efo/EFO_0009674 GCST90043807 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Headaches for three months (UKB data field 3799) 40,965 European ancestry cases, 48,784 European ancestry controls NA NR [11842647] (imputed) 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90043808 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of eye (PheCode 379) 194 European ancestry cases, 456,154 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90043809 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Otitis externa (PheCode 380.1) 409 European ancestry cases, 455,939 European ancestry controls NA NR [11842647] (imputed) 0 otitis externa http://www.ebi.ac.uk/efo/EFO_0009560 GCST90043810 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Impacted cerumen (PheCode 380.4) 212 European ancestry cases, 456,136 European ancestry controls NA NR [11842647] (imputed) 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90043811 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of external ear (PheCode 380) 616 European ancestry cases, 455,732 European ancestry controls NA NR [11842647] (imputed) 0 external ear disease http://www.ebi.ac.uk/efo/EFO_0009668 GCST90043812 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Suppurative and unspecified otitis media (PheCode 381.11) 634 European ancestry cases, 455,714 European ancestry controls NA NR [11842647] (imputed) 0 suppurative otitis media http://www.ebi.ac.uk/efo/EFO_0007503 GCST90043813 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Otitis media (PheCode 381.1) 1,039 European ancestry cases, 455,309 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043814 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eustachian tube disorders (PheCode 381.2) 169 European ancestry cases, 456,179 European ancestry controls NA NR [11842647] (imputed) 0 eustachian tube disease http://www.ebi.ac.uk/efo/EFO_0009667 GCST90043815 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mastoiditis & related conditions (PheCode 381.3) 124 European ancestry cases, 456,224 European ancestry controls NA NR [11842647] (imputed) 0 Mastoiditis http://purl.obolibrary.org/obo/HP_0000265 GCST90043816 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Otorrhea (PheCode 381.9) 183 European ancestry cases, 456,165 European ancestry controls NA NR [11842647] (imputed) 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90043817 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Otalgia (PheCode 382) 175 European ancestry cases, 456,173 European ancestry controls NA NR [11842647] (imputed) 0 Ear pain http://purl.obolibrary.org/obo/HP_0030766 GCST90043818 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Otosclerosis (PheCode 383) 288 European ancestry cases, 456,060 European ancestry controls NA NR [11842647] (imputed) 0 otosclerosis http://www.ebi.ac.uk/efo/EFO_0004213 GCST90043819 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Perforation of tympanic membrane (PheCode 384.4) 894 European ancestry cases, 455,454 European ancestry controls NA NR [11842647] (imputed) 0 tympanic membrane perforation http://www.ebi.ac.uk/efo/EFO_0009472 GCST90043820 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of tympanic membrane (PheCode 384) 203 European ancestry cases, 456,145 European ancestry controls NA NR [11842647] (imputed) 0 tympanic membrane disease http://www.ebi.ac.uk/efo/EFO_0009570 GCST90043821 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cholesteatoma (PheCode 385.3) 543 European ancestry cases, 455,805 European ancestry controls NA NR [11842647] (imputed) 0 cholesteatoma of middle ear http://www.ebi.ac.uk/efo/EFO_1000678 GCST90043822 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tympanosclerosis and middle ear disease related to otitis media (PheCode 385.5) 116 European ancestry cases, 456,232 European ancestry controls NA NR [11842647] (imputed) 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90043823 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason former drinker stopped drinking alcohol: Illness or ill health (UKB data field 3859_1) 4,074 European ancestry cases, 11,324 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043824 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason former drinker stopped drinking alcohol: Doctor's advice (UKB data field 3859_2) 859 European ancestry cases, 14,539 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043825 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason former drinker stopped drinking alcohol: Health precaution (UKB data field 3859_3) 3,119 European ancestry cases, 12,279 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043826 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason former drinker stopped drinking alcohol: Financial reasons (UKB data field 3859_4) 311 European ancestry cases, 15,087 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043827 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason former drinker stopped drinking alcohol: Other reason (UKB data field 3859_5) 7,035 European ancestry cases, 8,363 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043828 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Corneal dystrophy (PheCode 364.5) 125 European ancestry cases, 456,223 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90043779 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Corneal opacity and other disorders of cornea (PheCode 364) 124 European ancestry cases, 456,224 European ancestry controls NA NR [11842647] (imputed) 0 corneal disease http://www.ebi.ac.uk/efo/EFO_0009464 GCST90043780 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Primary open angle glaucoma (PheCode 365.11) 654 European ancestry cases, 455,694 European ancestry controls NA NR [11842647] (imputed) 0 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90043781 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Primary angle-closure glaucoma (PheCode 365.2) 591 European ancestry cases, 455,757 European ancestry controls NA NR [11842647] (imputed) 0 primary angle closure glaucoma http://www.ebi.ac.uk/efo/EFO_1001506 GCST90043782 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Glaucoma (PheCode 365) 1,190 European ancestry cases, 455,158 European ancestry controls NA NR [11842647] (imputed) 1 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90043783 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Senile cataract (PheCode 366.2) 8,734 European ancestry cases, 447,614 European ancestry controls NA NR [11842647] (imputed) 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90043784 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cataract (PheCode 366) 14,867 European ancestry cases, 441,481 European ancestry controls NA NR [11842647] (imputed) 1 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90043785 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diplopia and disorders of binocular vision (PheCode 368.2) 249 European ancestry cases, 456,099 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90043786 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Subjective visual disturbances (PheCode 368.9) 111 European ancestry cases, 456,237 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90043787 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Visual disturbances (PheCode 368) 365 European ancestry cases, 455,983 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043788 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Infection of the eye (PheCode 369) 182 European ancestry cases, 456,166 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90043789 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Corneal ulcer (PheCode 370.1) 130 European ancestry cases, 456,218 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90043790 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Uveitis, noninfectious or not otherwise specified (PheCode 371.1) 134 European ancestry cases, 456,214 European ancestry controls NA NR [11842647] (imputed) 0 Iridocyclitis http://purl.obolibrary.org/obo/HP_0001094 GCST90043791 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Inflammation of eyelids (PheCode 371.3) 2,119 European ancestry cases, 454,229 European ancestry controls NA NR [11842647] (imputed) 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90043792 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of conjunctiva (PheCode 372) 585 European ancestry cases, 455,763 European ancestry controls NA NR [11842647] (imputed) 0 Conjunctival Disorder http://www.ebi.ac.uk/efo/EFO_1000203 GCST90043793 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Former alcohol drinker (UKB data field 3731) 15,997 European ancestry cases, 14,532 European ancestry controls NA NR [11842647] (imputed) 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90043794 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ectropion or entropion (PheCode 374.1) 1,074 European ancestry cases, 455,274 European ancestry controls NA NR [11842647] (imputed) 0 entropion, ectropion http://purl.obolibrary.org/obo/MONDO_0001519, http://purl.obolibrary.org/obo/MONDO_0002043 GCST90043795 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ptosis of eyelid (PheCode 374.3) 1,797 European ancestry cases, 454,551 European ancestry controls NA NR [11842647] (imputed) 0 ptosis http://purl.obolibrary.org/obo/MONDO_0000728 GCST90043796 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Stomach abdominal pain for three months (UKB data field 3741) 21,320 European ancestry cases, 16,879 European ancestry controls NA NR [11842647] (imputed) 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90043797 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of eyelids (PheCode 374) 3,149 European ancestry cases, 453,199 European ancestry controls NA NR [11842647] (imputed) 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90043798 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Epiphora (PheCode 375.2) 774 European ancestry cases, 455,574 European ancestry controls NA NR [11842647] (imputed) 1 Epiphora http://purl.obolibrary.org/obo/HP_0009926 GCST90043799 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chest pain or discomfort when walking uphill or hurrying (UKB data field 3751) 15,207 European ancestry cases, 41,817 European ancestry controls NA NR [11842647] (imputed) 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90043800 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of lacrimal system (PheCode 375) 1,417 European ancestry cases, 454,931 European ancestry controls NA NR [11842647] (imputed) 0 dry eye syndrome http://www.ebi.ac.uk/efo/EFO_1000906 GCST90043801 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Optic neuritis/neuropathy (PheCode 377.3) 105 European ancestry cases, 456,243 European ancestry controls NA NR [11842647] (imputed) 0 optic neuritis http://www.ebi.ac.uk/efo/EFO_0007405 GCST90043802 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Knee pain for three months (UKB data field 3773) 75,940 European ancestry cases, 20,665 European ancestry controls NA NR [11842647] (imputed) 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90043803 Genome-wide genotyping array 2022-04-21 35393509 Loh M 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393509 Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. Type ii diabetes 16,677 South Asian ancestry cases, 33,856 South Asian ancestry controls NA NR [18881775] (imputed) 26 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90093109 Genome-wide genotyping array 2022-04-21 35393509 Loh M 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393509 Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. Type 2 diabetes (adjusted for BMI) 16,677 South Asian ancestry cases, 33,856 South Asian ancestry controls NA NR [18738826] (imputed) 24 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90093110 Genome-wide genotyping array 2022-04-21 35393509 Loh M 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393509 Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. Type ii diabetes 16,677 South Asian ancestry cases, 33,856 South Asian ancestry controls 231,420 European ancestry individuals NR [18881775] (imputed) 12 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90101836 Genome-wide genotyping array 2022-04-21 35393509 Loh M 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393509 Identification of genetic effects underlying type 2 diabetes in South Asian and European populations. Type 2 diabetes (adjusted for BMI) 16,677 South Asian ancestry cases, 33,856 South Asian ancestry controls 157,384 European ancestry individuals NR [18738826] (imputed) 10 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90101837 Genome-wide genotyping array 2022-03-10 35116054 Zhao F 2022-01-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/35116054 PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese Population. High myopia 507 Han Chinese ancestry cases, 294 Han Chinese ancestry controls 2,012 Han Chinese ancestry cases, 53,733 Han Chinese ancestry controls Illumina [NR] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90095188 Genome-wide genotyping array 2021-10-12 34226506 Cox J 2021-06-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226506 Genome-wide association study of stimulant dependence. Stimulant dependence 393 European ancestry cases, 5,287 European ancestry controls, 155 African American or Afro-Caribbean cases, 5,603 African American or Afro-Caribbean controls 532 European ancestry cases, 7,103 European ancestry controls, 53 African American or Afro-Caribbean cases, 3,299 African American or Afro-Caribbean controls Illumina [NR] (imputed) 8 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90026484 Genome-wide genotyping array 2021-10-12 34226506 Cox J 2021-06-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226506 Genome-wide association study of stimulant dependence. Stimulant dependence 393 European ancestry cases, 5,278 European ancestry controls 532 European ancestry cases, 7,103 European ancestry controls Illumina [NR] (imputed) 0 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90026485 Genome-wide genotyping array 2021-10-12 34226506 Cox J 2021-06-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226506 Genome-wide association study of stimulant dependence. Stimulant dependence 155 African American or Afro-Caribbean cases, 5,603 African American or Afro-Caribbean controls 53 African American or Afro-Caribbean cases, 3,299 African American or Afro-Caribbean controls Illumina [NR] (imputed) 12 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90026486 Genome-wide genotyping array 2022-03-02 33567813 Mateos MK 2021-02-11 Haematologica www.ncbi.nlm.nih.gov/pubmed/33567813 Methotrexate-related central neurotoxicity: clinical characteristics, risk factors and genome-wide association study in children treated for acute lymphoblastic leukemia. Methotrexate-related central neurotoxicity in children treated for acute lymphoblastic leukemia 48 European ancestry cases, 537 European ancestry controls NA Illumina [10838245] (imputed) 14 response to methotrexate, neurotoxicity http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0011057 GCST90095045 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (patient-rated acute xerostomia) 802 Dutch ancestry individuals 241 Dutch ancestry individuals Illumina [6334277] (imputed) 5 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095192 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (physician-rated acute xerostomia) 869 Dutch ancestry individuals 246 Dutch ancestry individuals Illumina [6334277] (imputed) 5 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095193 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (physician-rated acute dysphagia) 860 Dutch ancestry individuals 246 Dutch ancestry individuals Illumina [6334277] (imputed) 6 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095194 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (patient-rated acute sticky saliva) 799 Dutch ancestry individuals 214 Dutch ancestry individuals Illumina [6334277] (imputed) 9 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095195 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (physician-rated acute sticky saliva) 859 Dutch ancestry individuals 246 Dutch ancestry individuals Illumina [6334277] (imputed) 6 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095196 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (physician-rated acute mucositis) 864 Dutch ancestry individuals 246 Dutch ancestry individuals Illumina [6334277] (imputed) 8 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095197 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (standardized total average toxicity_physician) 881 Dutch ancestry individuals 246 Dutch ancestry individuals Illumina [6334277] (imputed) 3 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095198 Genome-wide genotyping array 2022-03-17 34838041 Naderi E 2021-11-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/34838041 A two-stage genome-wide association study of radiation-induced acute toxicity in head and neck cancer. radiation-induced toxicity (standardized total average toxicity_patient) 881 Dutch ancestry individuals 241 Dutch ancestry individuals Illumina [6334277] (imputed) 7 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90095199 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Body mass index 461,460 European ancestry individuals NA NR [NR] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90102533 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Systolic blood pressure 436,419 European ancestry individuals NA NR [NR] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90102534 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Diastolic blood pressure 436,424 European ancestry individuals NA NR [NR] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90102535 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. High density lipoprotein cholesterol levels 403,943 European ancestry individuals NA NR [NR] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90102536 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Low density lipoprotein cholesterol levels 440,546 European ancestry individuals NA NR [NR] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90102537 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Triglyceride levels 441,016 European ancestry individuals NA NR [NR] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102538 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Apolipoprotein B levels 439,214 European ancestry individuals NA NR [NR] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90102539 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Apolipoprotein A-I measurement 393,193 European ancestry individuals NA NR [NR] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90102540 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. C-reactive protein levels 438,131 European ancestry individuals NA NR [NR] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90102541 Genome-wide genotyping array 2022-05-10 35045726 Richardson TG 2022-01-20 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/35045726 Harnessing Whole Genome Polygenic Risk Scores to Stratify Individuals Based on Cardiometabolic Risk Factors and Biomarkers at Age 10 in the Lifecourse. Vitamin D levels 419,718 European ancestry individuals NA NR [NR] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90102542 Genome-wide genotyping array 2022-03-22 34827661 Emmert DB 2021-11-09 Biomolecules www.ncbi.nlm.nih.gov/pubmed/34827661 Genetic and Metabolic Determinants of Atrial Fibrillation in a General Population Sample: The CHRIS Study. Atrial fibrillation 110 European ancestry cases, 10,399 European ancestry controls NA Illumina [19057004] (imputed) 10 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90095475 Genome-wide genotyping array 2022-05-10 35086532 Li Y 2022-01-27 J Transl Med www.ncbi.nlm.nih.gov/pubmed/35086532 Polygenic risk and causal inference of psychiatric comorbidity in inflammatory bowel disease among patients with European ancestry. Psychiatric comorbidity in inflammatory bowel disease 94 European ancestry cases, 146 European ancestry controls NA Illumina [1267826] 0 psychiatric disorder http://purl.obolibrary.org/obo/MONDO_0002025 GCST90102545 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of pituitary gland and craniopharyngeal duct (pouch) (PheCode 227.3) 285 European ancestry cases, 456,063 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm of pituitary gland http://purl.obolibrary.org/obo/MONDO_0021439 GCST90043611 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemangioma and lymphangioma, any site (PheCode 228) 1,266 European ancestry cases, 455,082 European ancestry controls NA NR [11842647] (imputed) 0 lymphangioma, hemangioma http://purl.obolibrary.org/obo/MONDO_0002013, http://www.ebi.ac.uk/efo/EFO_1000635 GCST90043612 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of unspecified sites (PheCode 229) 2,201 European ancestry cases, 454,147 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90043613 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Wheeze or whistling in the chest in last year (UKB data field 2316) 93,869 European ancestry cases, 353,731 European ancestry controls NA NR [11842647] (imputed) 1 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90043614 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chest pain or discomfort (UKB data field 2335) 71,859 European ancestry cases, 379,675 European ancestry controls NA NR [11842647] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90043615 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair/balding pattern: Pattern 1 (UKB data field 2395_1) 66,172 European ancestry cases, 140,864 European ancestry controls NA NR [11842647] (imputed) 3 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST90043616 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair/balding pattern: Pattern 2 (UKB data field 2395_2) 47,867 European ancestry cases, 159,169 European ancestry controls NA NR [11842647] (imputed) 0 balding measurement, androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0007825, http://www.ebi.ac.uk/efo/EFO_0004191 GCST90043617 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair/balding pattern: Pattern 3 (UKB data field 2395_3) 55,137 European ancestry cases, 151,899 European ancestry controls NA NR [11842647] (imputed) 0 balding measurement, androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0007825, http://www.ebi.ac.uk/efo/EFO_0004191 GCST90043618 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hair/balding pattern: Pattern 4 (UKB data field 2395_4) 37,860 European ancestry cases, 169,176 European ancestry controls NA NR [11842647] (imputed) 1 balding measurement, androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0007825, http://www.ebi.ac.uk/efo/EFO_0004191 GCST90043619 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Simple and unspecified goiter (PheCode 240) 465 European ancestry cases, 455,883 European ancestry controls NA NR [11842647] (imputed) 0 goiter http://www.ebi.ac.uk/efo/EFO_0004283 GCST90043620 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nontoxic uninodular goiter (PheCode 241.1) 404 European ancestry cases, 455,944 European ancestry controls NA NR [11842647] (imputed) 0 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90043621 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nontoxic multinodular goiter (PheCode 241.2) 587 European ancestry cases, 455,761 European ancestry controls NA NR [11842647] (imputed) 0 nontoxic goiter, multinodular goiter http://purl.obolibrary.org/obo/MONDO_0001658, http://purl.obolibrary.org/obo/MONDO_0000334 GCST90043622 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Had major operations (UKB data field 2415) 133,145 European ancestry cases, 74,022 European ancestry controls NA NR [11842647] (imputed) 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90043623 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Graves' disease (PheCode 242.1) 210 European ancestry cases, 456,138 European ancestry controls NA NR [11842647] (imputed) 0 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST90043624 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Thyrotoxicosis with or without goiter (PheCode 242) 318 European ancestry cases, 456,030 European ancestry controls NA NR [11842647] (imputed) 0 hyperthyroidism, Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009189, http://www.ebi.ac.uk/efo/EFO_0009190 GCST90043625 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypothyroidism, not otherwise specified (PheCode 244.4) 145 European ancestry cases, 456,203 European ancestry controls NA NR [11842647] (imputed) 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90043626 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diabetes mellitus (UKB data field 2443) 21,969 European ancestry cases, 433,048 European ancestry controls NA NR [11842647] (imputed) 3 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90043627 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer (UKB data field 2453) 35,762 European ancestry cases, 418,974 European ancestry controls NA NR [11842647] (imputed) 1 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90043628 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bones in last 5 years (UKB data field 2463) 43,921 European ancestry cases, 409,903 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90043629 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: community worker, day centre officer, youth leader, youth worker, parish worker, bail support officer (UKB data field 22601_32313110) 1,347 European ancestry cases, 110,931 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043026 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: housing officer, welfare officer, refuge/rescue worker, probation assistant, nspcc inspector, day centre supervisor (UKB data field 22601_32323111) 319 European ancestry cases, 111,959 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043027 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: benefits advisor, citizens advice bureau adviser, debt counsellor (UKB data field 22601_32323112) 152 European ancestry cases, 112,126 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043028 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: school/student counsellor, school attendance officer (UKB data field 22601_32323410) 141 European ancestry cases, 112,137 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043029 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: non-commissioned officers or other rank of armed forces (UKB data field 22601_33113434) 2,480 European ancestry cases, 109,798 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043030 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: police officer (sergeant or below) (UKB data field 22601_33123442) 1,416 European ancestry cases, 110,862 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043031 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: fire service officer (leading fire officer and below) (UKB data field 22601_33133440) 234 European ancestry cases, 112,044 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043032 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: prison service officer (below principal officer), prison warder (UKB data field 22601_33143448) 132 European ancestry cases, 112,146 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043033 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: painter, calligrapher, portrait engraver, art restorer (UKB data field 22601_34113147) 105 European ancestry cases, 112,173 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043034 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: author, writer, biographer, book editor, novelist, dramatist, playwright, poet (UKB data field 22601_34123157) 355 European ancestry cases, 111,923 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043035 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: actor, chorister or singer (UKB data field 22601_34133166) 194 European ancestry cases, 112,084 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043036 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: musician, bandsman, instrumentalist, bellringer; composer, conductor; song writer (UKB data field 22601_34153170) 203 European ancestry cases, 112,075 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043037 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: arts officer, producer, director; entertainment/artists'/theatrical agent; studio manager, prompter (UKB data field 22601_34163176) 314 European ancestry cases, 111,964 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043038 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: graphic designer, commercial artist, desktop publishing artist, illuminator (UKB data field 22601_34213150) 406 European ancestry cases, 111,872 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043039 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: journalist, reporter, newspaper correspondent, sports writer, newspaper or magazine editor (UKB data field 22601_34313159) 617 European ancestry cases, 111,661 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043040 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: broadcasting professional, broadcaster, news reporter; radio or television journalist, director or producer (UKB data field 22601_34323160) 493 European ancestry cases, 111,785 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043041 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: public relations officer, press officer, information officer (UKB data field 22601_34333162) 151 European ancestry cases, 112,127 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043042 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: public relations officer, press officer, information officer, publicity assistant (UKB data field 22601_34333239) 507 European ancestry cases, 111,771 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043043 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: photographer and audio-visual equipment operator, cameraman, film technician, sound or light engineer, projectionist (UKB data field 22601_34343161) 439 European ancestry cases, 111,839 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043044 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sports coach, instructor, trainer, or manager (UKB data field 22601_34423138) 278 European ancestry cases, 112,000 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043045 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: aircraft pilot, flight engineer, aircraft navigator, helicopter pilot (UKB data field 22601_35122636) 124 European ancestry cases, 112,154 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043046 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: ship, merchant navy or hovercraft captain/officer/navigator, master mariner, skipper (UKB data field 22601_35132647) 201 European ancestry cases, 112,077 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043047 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: ship's engineer, ship's purser (UKB data field 22601_35132648) 193 European ancestry cases, 112,085 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043048 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: judge's or barrister's clerk, conveyancer, data protection officer, legal assistant or executive, coroner's officer, land registrar, tribunal member (UKB data field 22601_35203279) 175 European ancestry cases, 112,103 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043049 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: estimator, valuer, building estimator/assessor, insurance assessor, costing engineer, surveyor/valuer, lottery officer, rating officer, marine/naval surveyor (UKB data field 22601_35313264) 491 European ancestry cases, 111,787 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043050 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: laboratory technician (UKB data field 22601_31113086) 556 European ancestry cases, 111,722 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043001 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrical/electronics technician (UKB data field 22601_31122951) 440 European ancestry cases, 111,838 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043002 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrical or electronics technician, signals officer (UKB data field 22601_31123049) 653 European ancestry cases, 111,625 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043003 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: engineering technician, engineer's assistant, commissioning engineer, contracts engineer, technician engineer, industrial radiographer (UKB data field 22601_31133050) 1,120 European ancestry cases, 111,158 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043004 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: building or civil engineering technician, structural engineering technician, survey technician (UKB data field 22601_31143051) 151 European ancestry cases, 112,127 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043005 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: quality assurance technician/co-ordinator (UKB data field 22601_31152695) 299 European ancestry cases, 111,979 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043006 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: quality assurance technician or co-ordinator (UKB data field 22601_31153052) 139 European ancestry cases, 112,139 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043007 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other science technician, materials technician, technical assistant, technical officer (UKB data field 22601_31193034) 1,731 European ancestry cases, 110,547 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043008 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other engineering technician, including materials technician, technical assistant, technical officer (UKB data field 22601_31193055) 770 European ancestry cases, 111,508 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043009 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: architectural technologist/technician/assistant, town planning technician, planning enforcement officer (UKB data field 22601_31213292) 211 European ancestry cases, 112,067 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043010 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: draughtsperson, cartographer, designer-detailer/draughtsperson, drawing office checker, engineering draughtsperson (UKB data field 22601_31223293) 351 European ancestry cases, 111,927 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043011 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: it operations technician, computer operator or technician, database manager, network or web technician, web master, systems administrator or officer (UKB data field 22601_31313060) 1,336 European ancestry cases, 110,942 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043012 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: it user support technician, help desk or helpline operator (computing), support technician (computing), systems support officer (UKB data field 22601_31323061) 876 European ancestry cases, 111,402 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043013 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: nurse (of any kind, at any level) (UKB data field 22601_32113072) 6,089 European ancestry cases, 106,189 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043014 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: health visitor (UKB data field 22601_32113077) 500 European ancestry cases, 111,778 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043015 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: midwife (UKB data field 22601_32123074) 922 European ancestry cases, 111,356 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043016 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: medical radiographer, x-ray operator, sonographer (UKB data field 22601_32143084) 173 European ancestry cases, 112,105 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043017 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chiropodist, podiatrist (UKB data field 22601_32153081) 156 European ancestry cases, 112,122 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043018 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: pharmaceutical dispenser, pharmacy technician (UKB data field 22601_32173088) 203 European ancestry cases, 112,075 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043019 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: medical technician, audiologist, cardiographer, prosthesist, ecg technician, eeg technician (UKB data field 22601_32183085) 359 European ancestry cases, 111,919 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043020 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: dental technician, dental hygienist (UKB data field 22601_32183089) 98 European ancestry cases, 112,180 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043021 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: physiotherapist (UKB data field 22601_32213078) 583 European ancestry cases, 111,695 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043022 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: occupational therapist (UKB data field 22601_32223079) 366 European ancestry cases, 111,912 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043023 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: speech and language therapist (UKB data field 22601_32233080) 187 European ancestry cases, 112,091 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043024 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other therapist including acupuncturist, aromatherapist, dietician, herbalist, homeopath, hypnotherapist, masseur, orthoptist, osteopath, psychotherapist (UKB data field 22601_32293082) 1,075 European ancestry cases, 111,203 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043025 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: researcher in broadcasting, journalism, photography, printing and publishing (UKB data field 22601_23293164) 205 European ancestry cases, 112,073 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042976 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: solicitor, lawyer, barrister, judge, coroner, articled clerk, attorney, advocate, stipendiary magistrate, fiscal/crown prosecutor, sheriff (scottish courts), legal services recorder (UKB data field 22601_24113277) 1,320 European ancestry cases, 110,958 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042977 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other legal professional including: court clerk, legal officer/advisor, clerk to the justices, legal services registrar (UKB data field 22601_24193278) 225 European ancestry cases, 112,053 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042978 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chartered/certified accountant, auditor, company accountant, articled/audit clerk, official receiver (UKB data field 22601_24213281) 2,354 European ancestry cases, 109,924 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042979 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: management accountant, works accountant, cost accountant (UKB data field 22601_24223282) 943 European ancestry cases, 111,335 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042980 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: statistician (UKB data field 22601_24233025) 164 European ancestry cases, 112,114 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042981 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: management consultant, actuary, economist, statistician, statistical controller/assistant, business analyst, demographer, economic forecaster (UKB data field 22601_24233283) 1,137 European ancestry cases, 111,141 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042982 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: architect, landscape architect/designer, structural designer (UKB data field 22601_24312597) 444 European ancestry cases, 111,834 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042983 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: architect, landscape architect/designer, structural designer (UKB data field 22601_24313288) 518 European ancestry cases, 111,760 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042984 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: town planner, development officer (UKB data field 22601_24323289) 269 European ancestry cases, 112,009 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042985 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: quantity surveyor, quantity survey technician (UKB data field 22601_24332598) 415 European ancestry cases, 111,863 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042986 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: quantity surveyor, quantity survey technician (UKB data field 22601_24333290) 112 European ancestry cases, 112,166 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042987 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chartered surveyor, building surveyor, land surveyor (UKB data field 22601_24342599) 385 European ancestry cases, 111,893 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042988 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: river/water surveyor, surveyor and estimator, topographer, property surveyor (UKB data field 22601_24342600) 155 European ancestry cases, 112,123 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042989 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: surveyor in mining/minerals, energy production or water supply (UKB data field 22601_24342863) 108 European ancestry cases, 112,170 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042990 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chartered surveyor, building surveyor, land surveyor, mining/minerals surveyor, river/water surveyor, surveyor and estimator, topographer, property surveyor (UKB data field 22601_24343291) 351 European ancestry cases, 111,927 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042991 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: civil service senior manager outside the senior civil service (former grades 6 and 7) (UKB data field 22601_24413202) 1,621 European ancestry cases, 110,657 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042992 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: social worker, child care/protection officer, adoption officer, mental health officer, almoner, family case worker (UKB data field 22601_24423108) 1,940 European ancestry cases, 110,338 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042993 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: probation officer, community service officer (UKB data field 22601_24433109) 233 European ancestry cases, 112,045 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042994 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: clergyman/woman; any religious officer/leader (UKB data field 22601_24443114) 631 European ancestry cases, 111,647 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042995 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: librarian, assistant librarian (UKB data field 22601_24513035) 197 European ancestry cases, 112,081 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042996 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: librarian, assistant librarian (UKB data field 22601_24513314) 902 European ancestry cases, 111,376 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042997 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: librarian, assistant librarian (UKB data field 22601_24513424) 424 European ancestry cases, 111,854 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042998 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: archivist, curator, conservator, inspector of ancient monuments, museum officer (UKB data field 22601_24523188) 176 European ancestry cases, 112,102 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042999 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: laboratory technician, scientific assistant, cytology screener; hospital, medical or health technician (UKB data field 22601_31113033) 2,669 European ancestry cases, 109,609 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043000 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: careers adviser or vocational guidance specialist, placement advisor (UKB data field 22601_35643209) 239 European ancestry cases, 112,039 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043076 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: careers adviser or vocational guidance specialist, placement advisor (UKB data field 22601_35643215) 103 European ancestry cases, 112,175 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043077 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: health and safety officer, occupational hygienist, safety adviser (UKB data field 22601_35672595) 126 European ancestry cases, 112,152 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043078 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: health and safety officer, occupational hygienist, safety adviser (UKB data field 22601_35672697) 110 European ancestry cases, 112,168 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043079 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: health and safety officer, occupational hygienist, safety adviser, road safety officer (UKB data field 22601_35673467) 143 European ancestry cases, 112,135 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043080 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: civil service executive officer, revenue/tax executive or officer, fraud inspector or officer, job centre adviser (UKB data field 22601_41113204) 4,228 European ancestry cases, 108,050 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043081 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: civil service administrative officer or assistant or clerk, tax collector, prison service clerk, law courts clerk (UKB data field 22601_41123205) 5,059 European ancestry cases, 107,219 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043082 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: local government administrative officer or assistant or clerk (UKB data field 22601_41133206) 5,958 European ancestry cases, 106,320 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043083 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: officer of ngo, trade union organiser/official, charity administrator, secretary of research or charity or political or professional or trade association or trade union (UKB data field 22601_41143216) 1,993 European ancestry cases, 110,285 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043084 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: credit controller/supervisor (UKB data field 22601_41213240) 253 European ancestry cases, 112,025 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043085 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: credit controller/supervisor (UKB data field 22601_41213252) 245 European ancestry cases, 112,033 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043086 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: accounts and wages clerk/assistant/supervisor, bookkeeper, cost or ledger clerk, audit assistant, budget officer, student loans officer, paymaster (UKB data field 22601_41223241) 2,435 European ancestry cases, 109,843 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043087 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: accounts and wages clerk/assistant/supervisor, bookkeeper, cost or ledger clerk, audit assistant, budget officer, student loans officer, paymaster (UKB data field 22601_41223253) 1,141 European ancestry cases, 111,137 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043088 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: counter clerk, bank clerk, cashier, post office clerk (UKB data field 22601_41233254) 3,752 European ancestry cases, 108,526 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043089 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: ward clerk, medical records clerk (UKB data field 22601_41313093) 284 European ancestry cases, 111,994 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043090 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: filing clerk, records assistant/clerk (UKB data field 22601_41313256) 581 European ancestry cases, 111,697 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043091 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: filing clerk, records assistant/clerk (UKB data field 22601_41313272) 653 European ancestry cases, 111,625 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043092 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: filing clerk, records assistant/clerk, technical clerk, lottery clerk, courts administrator, checker, census enumerator, progress/document controller (UKB data field 22601_41313317) 301 European ancestry cases, 111,977 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043093 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: pensions and insurance clerk/administrator, claims handler (UKB data field 22601_41323255) 1,536 European ancestry cases, 110,742 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043094 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: stock control clerk, stock controller, progress/production/stock chaser, warehouse clerk, materials controller/co-ordinator, stores officer (UKB data field 22601_41333350) 383 European ancestry cases, 111,895 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043095 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: road transport/traffic clerk, distribution clerk/controller, shipping clerk/controller, fleet controller/administrator, traffic officer (road haulage) (UKB data field 22601_41342670) 285 European ancestry cases, 111,993 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043096 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: distribution clerk/controller, shipping clerk/controller, fleet controller/administrator, aircraft load controller/clerk, traffic officer (airlines, port, road haulage) (UKB data field 22601_41343351) 130 European ancestry cases, 112,148 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043097 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: library assistant/clerk, press cuttings clerk (UKB data field 22601_41353316) 764 European ancestry cases, 111,514 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043098 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: library assistant/clerk (UKB data field 22601_41353425) 182 European ancestry cases, 112,096 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043099 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: database assistant/clerk, computer clerk, data entry clerk/processor, book keeping/accounts machinist (UKB data field 22601_41363318) 584 European ancestry cases, 111,694 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043100 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: production and process engineer (UKB data field 22601_21273045) 429 European ancestry cases, 111,849 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042951 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: planning and quality control engineer, industrial engineer, quality engineer (UKB data field 22601_21283046) 351 European ancestry cases, 111,927 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042952 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other engineering professional (UKB data field 22601_21293047) 789 European ancestry cases, 111,489 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042953 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: it strategy or planning professional, computer consultant, software consultant (UKB data field 22601_21313058) 2,212 European ancestry cases, 110,066 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042954 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: software professional, analyst-programmer, computer programmer, software analyst or engineer, systems designer or programmer (UKB data field 22601_21323059) 4,256 European ancestry cases, 108,022 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042955 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: medical doctor, general practitioner, hospital consultant (UKB data field 22601_22113066) 1,831 European ancestry cases, 110,447 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042956 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: psychologist, psychometrist (UKB data field 22601_22123067) 359 European ancestry cases, 111,919 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042957 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: pharmacist, pharmacologist, pharmaceutical chemist (UKB data field 22601_22133068) 475 European ancestry cases, 111,803 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042958 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: ophthalmic optician, optometrist (UKB data field 22601_22143069) 128 European ancestry cases, 112,150 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042959 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: dentist, dental surgeon, orthodontist, periodontist (UKB data field 22601_22153070) 348 European ancestry cases, 111,930 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042960 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: university lecturer/professor (UKB data field 22601_23113030) 559 European ancestry cases, 111,719 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042961 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: higher education teaching professional, university lecturer/professor (including college/university head/vice chancellor) (UKB data field 22601_23113399) 3,311 European ancestry cases, 108,967 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042962 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: further education teaching professional, college lecturer/professor (UKB data field 22601_23123400) 3,055 European ancestry cases, 109,223 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042963 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: education officer, director of education, curriculum development officer (UKB data field 22601_23133420) 1,087 European ancestry cases, 111,191 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042964 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: school inspector, education inspector (UKB data field 22601_23133421) 288 European ancestry cases, 111,990 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042965 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: secondary school teacher or teaching professional (including head teacher) (UKB data field 22601_23143401) 9,356 European ancestry cases, 102,922 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042966 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: primary /junior school teacher or teaching professional, nursery school teacher (including head teacher) (UKB data field 22601_23153402) 6,903 European ancestry cases, 105,375 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042967 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: special needs teaching professional (including head teacher) (UKB data field 22601_23163403) 1,463 European ancestry cases, 110,815 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042968 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: registrar or senior administrator of educational establishment, bursar, registrar, university administrator (UKB data field 22601_23173422) 1,750 European ancestry cases, 110,528 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042969 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other teaching professional including private tutor, tefl (teaching english as a foreign language) teacher; tutor at adult education centre, etc. (UKB data field 22601_23193405) 1,748 European ancestry cases, 110,530 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042970 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: day nursery manager or owner (UKB data field 22601_23193429) 136 European ancestry cases, 112,142 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042971 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: scientific researcher, scientific officer, medical research associate, experimental officer (UKB data field 22601_23213026) 1,431 European ancestry cases, 110,847 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042972 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: social science researcher, anthropologist, sociologist, archaeologist, behavioural scientist, epidemiologist, government survey officer (UKB data field 22601_23223027) 509 European ancestry cases, 111,769 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042973 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: university research fellow or assistant/associate (UKB data field 22601_23293029) 885 European ancestry cases, 111,393 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042974 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other researchers including in broadcasting, journalism, photography, printing and publishing (UKB data field 22601_23293031) 189 European ancestry cases, 112,089 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042975 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: broker, financial/insurance broker, foreign exchange dealer, ship/marine broker, stockbroker, commodity trader (UKB data field 22601_35323258) 592 European ancestry cases, 111,686 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043051 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: broker, financial/insurance broker, foreign exchange dealer, ship/marine broker, stockbroker, commodity trader (UKB data field 22601_35323265) 272 European ancestry cases, 112,006 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043052 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: insurance underwriter, insurance inspector, insurance account handler (UKB data field 22601_35333259) 462 European ancestry cases, 111,816 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043053 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: insurance underwriter, insurance inspector, insurance account handler (UKB data field 22601_35333266) 181 European ancestry cases, 112,097 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043054 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: financial adviser/agent/consultant, investment analyst, mortgage consultant, financier, pension advisor (UKB data field 22601_35343267) 1,065 European ancestry cases, 111,213 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043055 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: taxation accountant or adviser or consultant or practitioner (UKB data field 22601_35353268) 303 European ancestry cases, 111,975 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043056 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: import agent, export agent, shipping agent (UKB data field 22601_35363269) 191 European ancestry cases, 112,087 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043057 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: financial controller, accounting/audit technician, trust officer (UKB data field 22601_35373270) 1,865 European ancestry cases, 110,413 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043058 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: festival organiser, events coordinator (UKB data field 22601_35393175) 103 European ancestry cases, 112,175 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043059 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: management information officer, conference/events co-ordinator/organiser, exhibition officer, work study engineer/officer/analyst, contract adviser/agent, election agent, business system analyst (UKB data field 22601_35393271) 2,275 European ancestry cases, 110,003 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043060 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: buyer, purchasing/procurement officer, supply officer (UKB data field 22601_35413236) 518 European ancestry cases, 111,760 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043061 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sales or marketing representative, manufacturer's agent or representative or salesman/woman (UKB data field 22601_35423237) 1,380 European ancestry cases, 110,898 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043062 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: marketing research professional, marketing consultant, promotions or advertising consultant, fundraiser consultant, appeals organiser (UKB data field 22601_35433238) 813 European ancestry cases, 111,465 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043063 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: estate agent, auctioneer, land agent, letting agent (UKB data field 22601_35443245) 356 European ancestry cases, 111,922 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043064 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: public service higher/senior executive officer, hospital administrator (UKB data field 22601_35613203) 3,965 European ancestry cases, 108,313 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043065 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: personnel or industrial relations officer, recruitment consultant (UKB data field 22601_35623207) 267 European ancestry cases, 112,011 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043066 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: personnel or industrial relations officer, recruitment consultant (UKB data field 22601_35623213) 488 European ancestry cases, 111,790 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043067 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: personnel or industrial relations officer, recruitment consultant (UKB data field 22601_35623217) 146 European ancestry cases, 112,132 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043068 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: personnel or industrial relations officer, recruitment consultant (UKB data field 22601_35623246) 661 European ancestry cases, 111,617 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043069 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: personnel or industrial relations officer, recruitment consultant (UKB data field 22601_35623273) 155 European ancestry cases, 112,123 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043070 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: vocational or industrial trainer/instructor (UKB data field 22601_35633208) 180 European ancestry cases, 112,098 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043071 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: vocational or industrial trainer/instructor, craft instructor, apprentice instructor (UKB data field 22601_35633214) 324 European ancestry cases, 111,954 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043072 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: vocational or industrial trainer/instructor (UKB data field 22601_35633218) 153 European ancestry cases, 112,125 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043073 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: vocational or industrial trainer/instructor (UKB data field 22601_35633247) 113 European ancestry cases, 112,165 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043074 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: vocational or industrial trainer/instructor (UKB data field 22601_35633274) 230 European ancestry cases, 112,048 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043075 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: database assistant/clerk, computer clerk, data entry clerk/processor, book keeping/accounts machinist (UKB data field 22601_41363428) 238 European ancestry cases, 112,040 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043101 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: market research interviewer, telephone interviewer (UKB data field 22601_41373244) 117 European ancestry cases, 112,161 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043102 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: telephonist, telephone/switchboard operator (UKB data field 22601_41413308) 857 European ancestry cases, 111,421 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043103 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: communication/telecommunications operator, radio/telex operator, radar operator (UKB data field 22601_41423309) 247 European ancestry cases, 112,031 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043104 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: emergency services control room/radio operator/officer (UKB data field 22601_41423445) 200 European ancestry cases, 112,078 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043105 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: general office assistant/clerk, clerical officer, clerk-typist, office supervisor, press/newspaper corrector/reader (UKB data field 22601_41503307) 5,024 European ancestry cases, 107,254 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043106 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: medical secretary (UKB data field 22601_42113094) 204 European ancestry cases, 112,074 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043107 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: medical secretary (UKB data field 22601_42113298) 1,072 European ancestry cases, 111,206 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043108 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: legal secretary, clerk, or aid clerk (UKB data field 22601_42123280) 564 European ancestry cases, 111,714 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043109 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: legal secretary (UKB data field 22601_42123299) 764 European ancestry cases, 61,821 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043110 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: school secretary (UKB data field 22601_42133300) 468 European ancestry cases, 62,117 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043111 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: school secretary, clerical assistant, school registry assistant (UKB data field 22601_42133407) 172 European ancestry cases, 62,413 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043112 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: school secretary, clerical assistant, school registry assistant (UKB data field 22601_42133423) 913 European ancestry cases, 111,365 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043113 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: company secretary, club secretary (UKB data field 22601_42143301) 233 European ancestry cases, 112,045 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043114 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: all other personal assistants and secretaries (UKB data field 22601_42153302) 6,760 European ancestry cases, 105,518 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043115 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: receptionist, doctor's/dental receptionist (UKB data field 22601_42163095) 386 European ancestry cases, 111,892 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043116 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: receptionist, doctor's/dental receptionist (UKB data field 22601_42163303) 1,392 European ancestry cases, 110,886 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043117 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: typist, shorthand typist, transcriber, stenographer (UKB data field 22601_42173304) 3,774 European ancestry cases, 108,504 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043118 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: farmer, farming contractor, herd manager, smallholder, bailiff (UKB data field 22601_51112476) 222 European ancestry cases, 112,056 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043119 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: nurseryman, market gardener, horticulturist (UKB data field 22601_51122486) 198 European ancestry cases, 112,080 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043120 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: gardener, groundsman/groundswoman, park keeper, landscape gardener, greenkeeper, turf cutter (UKB data field 22601_51132488) 697 European ancestry cases, 111,581 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043121 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sheet metal worker, panel beater, metal finisher, coppersmith (UKB data field 22601_52132923) 172 European ancestry cases, 112,106 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043122 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: metal plate worker, boilermaker, plater-welder, caulker-burner, shipwright, riveter (UKB data field 22601_52142924) 189 European ancestry cases, 49,504 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043123 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: welder, fitter-welder (UKB data field 22601_52152925) 231 European ancestry cases, 112,047 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043124 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: pipe fitter (UKB data field 22601_52162926) 162 European ancestry cases, 49,531 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043125 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: metal machine setter, tool setter, setter operator, centre lathe turner (UKB data field 22601_52212927) 404 European ancestry cases, 111,874 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043126 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: tool maker, tool fitter, jig and tool fitter, marker out, die sinker (UKB data field 22601_52222928) 382 European ancestry cases, 111,896 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043127 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: plant maintenance fitter, machine fitter, mechanic-fitter (UKB data field 22601_52232856) 280 European ancestry cases, 49,413 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043128 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: metal working production or maintenance fitter, machine fitter, fitter and turner, bench fitter, plant fitter (UKB data field 22601_52232929) 684 European ancestry cases, 111,594 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043129 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: motor vehicle/industrial machinery fitter (UKB data field 22601_52232941) 205 European ancestry cases, 112,073 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043130 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: aircraft engineer (UKB data field 22601_52232942) 171 European ancestry cases, 112,107 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043131 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: motor mechanic, auto engineer (UKB data field 22601_52312660) 296 European ancestry cases, 111,982 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043132 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: motor mechanic, diesel fitter, auto engineer (UKB data field 22601_52312934) 677 European ancestry cases, 111,601 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043133 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: vehicle body builder, coach builder, panel beater (UKB data field 22601_52322935) 115 European ancestry cases, 112,163 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043134 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrician, electrical fitter (UKB data field 22601_52412528) 102 European ancestry cases, 49,591 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043135 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrician, electrical fitter (UKB data field 22601_52412543) 500 European ancestry cases, 111,778 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043136 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrician, electrical engineer, electrical contractor (UKB data field 22601_52412944) 821 European ancestry cases, 111,457 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043137 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: telecommunication engineer, telephone engineer, telephone technician (UKB data field 22601_52422945) 469 European ancestry cases, 111,809 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043138 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: television or radio engineer, video engineer (UKB data field 22601_52442947) 157 European ancestry cases, 112,121 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043139 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: television, video, audio or radio engineer/repairer/installer/technician (UKB data field 22601_52443062) 138 European ancestry cases, 112,140 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043140 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: computer engineer, computer service or maintenance technician (UKB data field 22601_52452948) 148 European ancestry cases, 112,130 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043141 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: computer installation and maintenance engineer/repairer/installer/technician (UKB data field 22601_52453063) 368 European ancestry cases, 111,910 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043142 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electronic engineer (maintenance), alarm engineer, office equipment engineer (UKB data field 22601_52492949) 227 European ancestry cases, 112,051 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043143 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: other electrical or electronics technician, including alarm engineer, office machinery engineer or mechanic (UKB data field 22601_52493053) 366 European ancestry cases, 111,912 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043144 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: bricklayer (UKB data field 22601_53122524) 164 European ancestry cases, 49,529 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043145 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: plumber (UKB data field 22601_53142539) 242 European ancestry cases, 112,036 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043146 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: heating engineer, gas service engineer, air conditioning engineer (UKB data field 22601_53142540) 296 European ancestry cases, 111,982 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043147 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: carpenter, carpenter and joiner, builder's joiner (UKB data field 22601_53152529) 243 European ancestry cases, 112,035 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043148 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: carpenter, carpenter and joiner, builder's joiner (UKB data field 22601_53152546) 504 European ancestry cases, 111,774 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043149 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: builder, building contractor (UKB data field 22601_53192534) 144 European ancestry cases, 112,134 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043150 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Heavy goods vehicle drivers (UKB data field 22617_8211) 864 European ancestry cases, 112,977 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043552 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Convulsions (PheCode 345.3) 1,567 European ancestry cases, 454,781 European ancestry controls NA NR [11842647] (imputed) 0 Seizure http://purl.obolibrary.org/obo/HP_0001250 GCST90043756 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Epilepsy, recurrent seizures, convulsions (PheCode 345) 799 European ancestry cases, 455,549 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the nervous system http://purl.obolibrary.org/obo/HP_0000707 GCST90043757 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other conditions of brain, not otherwise specified (PheCode 348.9) 170 European ancestry cases, 456,178 European ancestry controls NA NR [11842647] (imputed) 0 brain disease http://www.ebi.ac.uk/efo/EFO_0005774 GCST90043758 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other and unspecified disorders of the nervous system (PheCode 349) 173 European ancestry cases, 456,175 European ancestry controls NA NR [11842647] (imputed) 0 secondary Parkinson disease http://www.ebi.ac.uk/efo/EFO_1001175 GCST90043759 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal involuntary movements (PheCode 350.1) 330 European ancestry cases, 456,018 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043760 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormality of gait (PheCode 350.2) 412 European ancestry cases, 455,936 European ancestry controls NA NR [11842647] (imputed) 0 Gait disturbance http://purl.obolibrary.org/obo/HP_0001288 GCST90043761 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Lack of coordination (PheCode 350.3) 123 European ancestry cases, 456,225 European ancestry controls NA NR [11842647] (imputed) 0 Dystonia http://purl.obolibrary.org/obo/HP_0001332 GCST90043762 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other peripheral nerve disorders (PheCode 351) 12,887 European ancestry cases, 443,461 European ancestry controls NA NR [11842647] (imputed) 0 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90043763 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Trigeminal nerve disorders [CN5] (PheCode 352.1) 293 European ancestry cases, 456,055 European ancestry controls NA NR [11842647] (imputed) 0 trigeminal nerve disease http://www.ebi.ac.uk/efo/EFO_0009569 GCST90043764 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Facial nerve disorders [CN7] (PheCode 352.2) 536 European ancestry cases, 455,812 European ancestry controls NA NR [11842647] (imputed) 0 facial nerve disease http://www.ebi.ac.uk/efo/EFO_1002051 GCST90043765 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nerve root and plexus disorders (PheCode 353) 133 European ancestry cases, 456,215 European ancestry controls NA NR [11842647] (imputed) 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90043766 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Back pain for three months (UKB data field 3571) 79,258 European ancestry cases, 36,221 European ancestry controls NA NR [11842647] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90043767 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Inflammatory and toxic neuropathy (PheCode 357) 625 European ancestry cases, 455,723 European ancestry controls NA NR [11842647] (imputed) 0 chronic inflammatory demyelinating polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009538 GCST90043768 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Myasthenia gravis (PheCode 358.1) 124 European ancestry cases, 456,224 European ancestry controls NA NR [11842647] (imputed) 0 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST90043769 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Myopathy (PheCode 359.2) 226 European ancestry cases, 456,122 European ancestry controls NA NR [11842647] (imputed) 1 myositis http://www.ebi.ac.uk/efo/EFO_0000783 GCST90043770 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ever had hysterectomy - womb removed (UKB data field 3591) 17,911 European ancestry cases, 200,558 European ancestry controls NA NR [11842647] (imputed) 0 hysterectomy http://www.ebi.ac.uk/efo/EFO_0003881 GCST90043771 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chest pain or discomfort walking normally (UKB data field 3606) 12,557 European ancestry cases, 58,657 European ancestry controls NA NR [11842647] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90043772 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Retinal detachment with retinal defect (PheCode 361.1) 1,474 European ancestry cases, 454,874 European ancestry controls NA NR [11842647] (imputed) 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90043773 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chest pain due to walking ceases when standing still (UKB data field 3616) 21,099 European ancestry cases, 4,967 European ancestry controls NA NR [11842647] (imputed) 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90043774 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Retinal detachments and defects (PheCode 361) 2,128 European ancestry cases, 454,220 European ancestry controls NA NR [11842647] (imputed) 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90043775 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Macular degeneration (senile) of retina, not otherwise specified (PheCode 362.29) 1,295 European ancestry cases, 455,053 European ancestry controls NA NR [11842647] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90043776 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Retinal vascular changes and abnomalities (PheCode 362.4) 593 European ancestry cases, 455,755 European ancestry controls NA NR [11842647] (imputed) 0 retinal vein occlusion http://www.ebi.ac.uk/efo/EFO_1001157 GCST90043777 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other retinal disorders (PheCode 362) 605 European ancestry cases, 455,743 European ancestry controls NA NR [11842647] (imputed) 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90043778 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Glass and ceramics makers, decorators and finishers (UKB data field 22617_5491) 101 European ancestry cases, 113,740 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043501 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Furniture makers, other craft woodworkers (UKB data field 22617_5492) 243 European ancestry cases, 113,598 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043502 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Hand craft occupations n.e.c. (UKB data field 22617_5499) 137 European ancestry cases, 113,704 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043503 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Nursing auxiliaries and assistants (UKB data field 22617_6111) 1,632 European ancestry cases, 112,209 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043504 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Ambulance staff (excluding paramedics) (UKB data field 22617_6112) 101 European ancestry cases, 113,740 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043505 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Dental nurses (UKB data field 22617_6113) 286 European ancestry cases, 113,555 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043506 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Houseparents and residential wardens (UKB data field 22617_6114) 841 European ancestry cases, 113,000 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043507 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Care assistants and home carers (UKB data field 22617_6115) 1,566 European ancestry cases, 112,275 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043508 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Nursery nurses (UKB data field 22617_6121) 418 European ancestry cases, 113,423 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043509 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Childminders and related occupations (UKB data field 22617_6122) 1,157 European ancestry cases, 112,684 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043510 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Playgroup leaders/assistants (UKB data field 22617_6123) 580 European ancestry cases, 113,261 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043511 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Educational assistants (UKB data field 22617_6124) 2,871 European ancestry cases, 110,970 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043512 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Veterinary nurses and assistants (UKB data field 22617_6131) 172 European ancestry cases, 113,669 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043513 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Animal care occupations n.e.c. (UKB data field 22617_6139) 208 European ancestry cases, 113,633 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043514 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Sports and leisure assistants (UKB data field 22617_6211) 274 European ancestry cases, 113,567 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043515 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Travel agents (UKB data field 22617_6212) 517 European ancestry cases, 113,324 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043516 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Travel and tour guides (UKB data field 22617_6213) 259 European ancestry cases, 113,582 European ancestry controls NA NR [11842647] (imputed) 1 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043517 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Air travel assistants (UKB data field 22617_6214) 453 European ancestry cases, 113,388 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043518 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Rail travel assistants (UKB data field 22617_6215) 123 European ancestry cases, 113,718 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043519 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Leisure and travel service occupations n.e.c. (UKB data field 22617_6219) 256 European ancestry cases, 113,585 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043520 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Hairdressers, barbers (UKB data field 22617_6221) 535 European ancestry cases, 113,306 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043521 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Beauticians and related occupations (UKB data field 22617_6222) 129 European ancestry cases, 113,712 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043522 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Housekeepers and related occupations (UKB data field 22617_6231) 430 European ancestry cases, 113,411 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043523 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Caretakers (UKB data field 22617_6232) 376 European ancestry cases, 113,465 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043524 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Sales and retail assistants (UKB data field 22617_7111) 5,914 European ancestry cases, 107,927 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043525 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Retail cashiers and check-out operators (UKB data field 22617_7112) 1,157 European ancestry cases, 112,684 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043526 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Collector salespersons and credit agents (UKB data field 22617_7121) 1,027 European ancestry cases, 112,814 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043527 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Roundsmen/women and van salespersons (UKB data field 22617_7123) 330 European ancestry cases, 113,511 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043528 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Market and street traders and assistants (UKB data field 22617_7124) 126 European ancestry cases, 113,715 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043529 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Merchandisers and window dressers (UKB data field 22617_7125) 245 European ancestry cases, 113,596 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043530 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Sales related occupations n.e.c. (UKB data field 22617_7129) 1,330 European ancestry cases, 112,511 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043531 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Call centre agents/operators (UKB data field 22617_7211) 995 European ancestry cases, 112,846 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043532 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Customer care occupations (UKB data field 22617_7212) 2,150 European ancestry cases, 111,691 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043533 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Food, drink and tobacco process operatives (UKB data field 22617_8111) 298 European ancestry cases, 113,543 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043534 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Textile process operatives (UKB data field 22617_8113) 334 European ancestry cases, 113,507 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043535 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Chemical and related process operatives (UKB data field 22617_8114) 196 European ancestry cases, 113,645 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043536 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Plastics process operatives (UKB data field 22617_8116) 230 European ancestry cases, 113,611 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043537 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Metal making and treating process operatives (UKB data field 22617_8117) 157 European ancestry cases, 113,684 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043538 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Paper and wood machine operatives (UKB data field 22617_8121) 209 European ancestry cases, 113,632 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043539 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Coal mine operatives (UKB data field 22617_8122) 340 European ancestry cases, 113,501 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043540 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Energy plant operatives (UKB data field 22617_8124) 128 European ancestry cases, 50,521 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043541 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Metal working machine operatives (UKB data field 22617_8125) 174 European ancestry cases, 113,667 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043542 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Assemblers (electrical products) (UKB data field 22617_8131) 547 European ancestry cases, 113,294 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043543 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Assemblers (vehicles and metal goods) (UKB data field 22617_8132) 686 European ancestry cases, 113,155 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043544 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Routine inspectors and testers (UKB data field 22617_8133) 506 European ancestry cases, 113,335 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043545 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Weighers, graders, sorters (UKB data field 22617_8134) 217 European ancestry cases, 113,624 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043546 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Sewing machinists (UKB data field 22617_8137) 604 European ancestry cases, 113,237 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043547 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Routine laboratory testers (UKB data field 22617_8138) 281 European ancestry cases, 113,560 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043548 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Assemblers and routine operatives n.e.c. (UKB data field 22617_8139) 1,599 European ancestry cases, 112,242 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043549 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Road construction operatives (UKB data field 22617_8142) 131 European ancestry cases, 113,710 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043550 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Metal machining setters and setter-operators (UKB data field 22617_5221) 415 European ancestry cases, 113,426 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043476 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Tool makers, tool fitters and markers-out (UKB data field 22617_5222) 394 European ancestry cases, 113,447 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043477 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Metal working production and maintenance fitters (UKB data field 22617_5223) 1,520 European ancestry cases, 112,321 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043478 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Precision instrument makers and repairers (UKB data field 22617_5224) 101 European ancestry cases, 113,740 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043479 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Motor mechanics, auto engineers (UKB data field 22617_5231) 980 European ancestry cases, 112,861 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043480 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Vehicle body builders and repairers (UKB data field 22617_5232) 183 European ancestry cases, 113,658 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043481 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Electricians, electrical fitters (UKB data field 22617_5241) 1,358 European ancestry cases, 112,483 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043482 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Telecommunications engineers (UKB data field 22617_5242) 485 European ancestry cases, 113,356 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043483 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: TV, video and audio engineers (UKB data field 22617_5244) 296 European ancestry cases, 113,545 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043484 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Computer engineers, installation and maintenance (UKB data field 22617_5245) 530 European ancestry cases, 113,311 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043485 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Electrical/electronics engineers n.e.c. (UKB data field 22617_5249) 701 European ancestry cases, 113,140 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043486 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Bricklayers, masons (UKB data field 22617_5312) 207 European ancestry cases, 113,634 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043487 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Plumbers, heating and ventilating engineers (UKB data field 22617_5314) 538 European ancestry cases, 113,303 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043488 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Carpenters and joiners (UKB data field 22617_5315) 748 European ancestry cases, 113,093 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043489 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Construction trades n.e.c. (UKB data field 22617_5319) 357 European ancestry cases, 113,484 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043490 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Painters and decorators (UKB data field 22617_5323) 459 European ancestry cases, 113,382 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043491 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Weavers and knitters (UKB data field 22617_5411) 112 European ancestry cases, 113,729 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043492 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Upholsterers (UKB data field 22617_5412) 126 European ancestry cases, 113,715 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043493 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Tailors and dressmakers (UKB data field 22617_5414) 213 European ancestry cases, 113,628 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043494 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Originators, compositors and print preparers (UKB data field 22617_5421) 234 European ancestry cases, 113,607 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043495 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Printers (UKB data field 22617_5422) 144 European ancestry cases, 113,697 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043496 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Bookbinders and print finishers (UKB data field 22617_5423) 114 European ancestry cases, 113,727 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043497 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Butchers, meat cutters (UKB data field 22617_5431) 107 European ancestry cases, 113,734 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043498 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Bakers, flour confectioners (UKB data field 22617_5432) 236 European ancestry cases, 113,605 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043499 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Chefs, cooks (UKB data field 22617_5434) 1,041 European ancestry cases, 112,800 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043500 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Filing and other records assistants/clerks (UKB data field 22617_4131) 1,941 European ancestry cases, 111,900 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043451 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Pensions and insurance clerks (UKB data field 22617_4132) 1,559 European ancestry cases, 112,282 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043452 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Stock control clerks (UKB data field 22617_4133) 393 European ancestry cases, 113,448 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043453 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Transport and distribution clerks (UKB data field 22617_4134) 553 European ancestry cases, 113,288 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043454 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Library assistants/clerks (UKB data field 22617_4135) 941 European ancestry cases, 112,900 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043455 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Database assistants/clerks (UKB data field 22617_4136) 833 European ancestry cases, 113,008 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043456 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Market research interviewers (UKB data field 22617_4137) 118 European ancestry cases, 113,723 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043457 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Telephonists (UKB data field 22617_4141) 870 European ancestry cases, 112,971 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043458 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Communication operators (UKB data field 22617_4142) 518 European ancestry cases, 113,323 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043459 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: General office assistants/clerks (UKB data field 22617_4150) 5,095 European ancestry cases, 108,746 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043460 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Medical secretaries (UKB data field 22617_4211) 1,288 European ancestry cases, 112,553 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043461 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Legal secretaries (UKB data field 22617_4212) 1,313 European ancestry cases, 112,528 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043462 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: School secretaries (UKB data field 22617_4213) 1,548 European ancestry cases, 112,293 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043463 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Company secretaries (UKB data field 22617_4214) 236 European ancestry cases, 113,605 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043464 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Personal assistants and other secretaries (UKB data field 22617_4215) 6,855 European ancestry cases, 106,986 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043465 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Receptionists (UKB data field 22617_4216) 1,787 European ancestry cases, 112,054 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043466 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Typists (UKB data field 22617_4217) 3,828 European ancestry cases, 110,013 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043467 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Farmers (UKB data field 22617_5111) 227 European ancestry cases, 113,614 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043468 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Horticultural trades (UKB data field 22617_5112) 199 European ancestry cases, 113,642 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043469 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Gardeners and groundsmen/groundswomen (UKB data field 22617_5113) 707 European ancestry cases, 113,134 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043470 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Agricultural and fishing trades n.e.c. (UKB data field 22617_5119) 128 European ancestry cases, 113,713 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043471 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Sheet metal workers (UKB data field 22617_5213) 173 European ancestry cases, 113,668 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043472 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Metal plate workers, shipwrights, riveters (UKB data field 22617_5214) 340 European ancestry cases, 113,501 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043473 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Welding trades (UKB data field 22617_5215) 346 European ancestry cases, 113,495 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043474 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Pipe fitters (UKB data field 22617_5216) 282 European ancestry cases, 50,367 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043475 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Construction operatives n.e.c. (UKB data field 22617_8149) 485 European ancestry cases, 113,356 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043551 Genome-wide genotyping array 2022-04-29 34850884 Suetsugu H 2021-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34850884 Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus. Steroid induced osteonecrosis of the femoral head and systemic lupus erythematosus 636 Japanese ancestry cases, 95,588 Japanese ancestry controls NA Illumina [NR] (imputed) 16 response to steroid, systemic lupus erythematosus, idiopathic osteonecrosis of the femoral head http://www.ebi.ac.uk/efo/EFO_0020976, http://purl.obolibrary.org/obo/MONDO_0007915, http://www.ebi.ac.uk/efo/EFO_1001930 GCST90102276 Genome-wide genotyping array 2022-04-29 34850884 Suetsugu H 2021-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34850884 Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus. Steroid induced osteonecrosis of the femoral head in systemic lupus erythematosus 636 Japanese ancestry cases, 683 Japanese ancestry controls NA Illumina [NR] (imputed) 1 response to steroid, idiopathic osteonecrosis of the femoral head http://www.ebi.ac.uk/efo/EFO_0020976, http://www.ebi.ac.uk/efo/EFO_1001930 GCST90102277 Genome-wide genotyping array 2022-04-29 34850884 Suetsugu H 2021-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34850884 Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus. Systemic lupus erythematosus 683 Japanese ancestry cases, 95,588 Japanese ancestry controls NA Illumina [NR] (imputed) 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90102278 Genome-wide genotyping array 2022-04-29 34850884 Suetsugu H 2021-12-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34850884 Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus. Steroid induced osteonecrosis of the femoral head and systemic lupus erythematosus 784 East Asian ancestry cases, 132,603 East Asian ancestry controls NA Illumina [NR] (imputed) 4 response to steroid, systemic lupus erythematosus, idiopathic osteonecrosis of the femoral head http://www.ebi.ac.uk/efo/EFO_0020976, http://purl.obolibrary.org/obo/MONDO_0007915, http://www.ebi.ac.uk/efo/EFO_1001930 GCST90102279 Genome-wide genotyping array 2022-03-22 34834527 Park S 2021-11-10 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834527 Interaction of Polygenetic Variants for Gestational Diabetes Mellitus Risk with Breastfeeding and Korean Balanced Diet to Influence Type 2 Diabetes Risk in Later Life in a Large Hospital-Based Cohort. Gestational diabetes mellitus 384 cases, 33,956 controls NA Affymetrix [NR] 3 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST90095480 Genome-wide genotyping array 2021-11-24 34737425 Mansour Aly D 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737425 Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes. Severe autoimmune type 2 diabetes 452 Scandinavian ancestry cases, 2,744 Scandinavian ancestry controls NA Illumina [5396854] (imputed) 16 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90026412 Genome-wide genotyping array 2021-11-24 34737425 Mansour Aly D 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737425 Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes. Severe insulin-deficient type 2 diabetes 1,193 Scandinavian ancestry cases, 2,744 Scandinavian ancestry controls NA Illumina [5398302] (imputed) 16 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90026413 Genome-wide genotyping array 2021-11-24 34737425 Mansour Aly D 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737425 Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes. Severe insulin-resistant type 2 diabetes 1,130 Scandinavian ancestry cases, 2,744 Scandinavian ancestry controls NA Illumina [5397362] (imputed) 12 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90026414 Genome-wide genotyping array 2021-11-24 34737425 Mansour Aly D 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737425 Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes. Mild obesity-related type 2 diabetes 1,374 Scandinavian ancestry cases, 2,744 Scandinavian ancestry controls NA Illumina [5400100] (imputed) 14 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90026415 Genome-wide genotyping array 2021-11-24 34737425 Mansour Aly D 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737425 Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes. Mild age-related type 2 diabetes 2,861 Scandinavian ancestry cases, 2,744 Scandinavian ancestry controls NA Illumina [5397657] (imputed) 21 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90026416 Genome-wide genotyping array 2021-11-24 34737425 Mansour Aly D 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737425 Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes. Type 2 diabetes 9,486 Scandinavian ancestry cases, 2,744 Scandinavian ancestry controls NA Illumina [5399457] (imputed) 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90026417 Genome-wide genotyping array 2021-12-02 34785669 Grosche S 2021-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34785669 Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4. Eczema 20,016 European ancestry cases, 380,433 European ancestry controls NA Affymetrix, Illumina [9397031] (imputed) 48 Eczema http://purl.obolibrary.org/obo/HP_0000964 GCST90044763 Genome-wide genotyping array 2022-05-13 35379913 Sharafeldin N 2022-04-04 Bone Marrow Transplant www.ncbi.nlm.nih.gov/pubmed/35379913 Genome-wide variants and polygenic risk scores for cognitive impairment following blood or marrow transplantation. Cognitive impairment in blood or marrow transplantation (additive genetic model) 165 European ancestry individuals, 74 individuals 432 European ancestry individuals, 108 individuals NR [142853] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90102514 Genome-wide genotyping array 2022-05-13 35379913 Sharafeldin N 2022-04-04 Bone Marrow Transplant www.ncbi.nlm.nih.gov/pubmed/35379913 Genome-wide variants and polygenic risk scores for cognitive impairment following blood or marrow transplantation. Cognitive impairment in blood or marrow transplantation (codominant genetic model) 165 European ancestry individuals, 74 individuals 432 European ancestry individuals, 108 individuals NR [142853] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90102515 Genome-wide genotyping array 2022-05-13 35379913 Sharafeldin N 2022-04-04 Bone Marrow Transplant www.ncbi.nlm.nih.gov/pubmed/35379913 Genome-wide variants and polygenic risk scores for cognitive impairment following blood or marrow transplantation. Cognitive impairment in blood or marrow transplantation (dominant/recessive genetic model) 165 European ancestry individuals, 74 individuals 432 European ancestry individuals, 108 individuals NR [142853] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90102516 Genome-wide genotyping array 2022-04-06 34865661 Meijsen JJ 2021-12-06 Psychol Med www.ncbi.nlm.nih.gov/pubmed/34865661 Shared genetic influences on depression and menopause symptoms. Medication use (estrogens) up to 10,103 European ancestry cases, up to 222,890 European ancestry controls NA NR [NR] (imputed) 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90101716 Genome-wide genotyping array 2022-04-06 34865661 Meijsen JJ 2021-12-06 Psychol Med www.ncbi.nlm.nih.gov/pubmed/34865661 Shared genetic influences on depression and menopause symptoms. Medication use (estrogens and progestogens) 14,843 European ancestry cases, 205,272 European ancestry controls NA NR [NR] (imputed) 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90101717 Genome-wide genotyping array 2022-04-06 34865661 Meijsen JJ 2021-12-06 Psychol Med www.ncbi.nlm.nih.gov/pubmed/34865661 Shared genetic influences on depression and menopause symptoms. Medication use (estrogens) 10,103 European ancestry, African ancestry, Asian ancestry, unknown ancestry cases, 222,890 European ancestry, African ancestry, Asian ancestry, unknown ancestry controls NA NR [NR] (imputed) 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90101718 Genome-wide genotyping array 2022-04-06 34865661 Meijsen JJ 2021-12-06 Psychol Med www.ncbi.nlm.nih.gov/pubmed/34865661 Shared genetic influences on depression and menopause symptoms. Medication use (estrogens and progestogens) 14,843 European ancestry cases, 205,272 European ancestry controls, 116 Black cases, 3,926 Black controls, 153 Asian ancestry cases, 4,813 Asian ancestry controls, 193 cases, 3,677 controls NA NR [NR] (imputed) 1 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90101719 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anterior horn cell disease (PheCode 334.2) 169 European ancestry cases, 456,179 European ancestry controls NA NR [11842647] (imputed) 0 anterior horn disorder http://purl.obolibrary.org/obo/MONDO_0003182 GCST90043736 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Degenerative disease of the spinal cord (PheCode 334) 387 European ancestry cases, 455,961 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90043737 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Multiple sclerosis (PheCode 335) 775 European ancestry cases, 455,573 European ancestry controls NA NR [11842647] (imputed) 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90043738 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute pain (PheCode 338.1) 204 European ancestry cases, 456,144 European ancestry controls NA NR [11842647] (imputed) 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90043739 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic pain (PheCode 338.2) 152 European ancestry cases, 456,196 European ancestry controls NA NR [11842647] (imputed) 0 Chronic pain http://purl.obolibrary.org/obo/HP_0012532 GCST90043740 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hearing aid user (UKB data field 3393) 13,905 European ancestry cases, 262,475 European ancestry controls NA NR [11842647] (imputed) 1 able to hear with hearing aids http://www.ebi.ac.uk/efo/EFO_0009720 GCST90043741 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other headache syndromes (PheCode 339) 5,724 European ancestry cases, 450,624 European ancestry controls NA NR [11842647] (imputed) 0 headache disorder http://www.ebi.ac.uk/efo/EFO_0009550 GCST90043742 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Migrain with aura (PheCode 340.1) 166 European ancestry cases, 456,182 European ancestry controls NA NR [11842647] (imputed) 0 migraine with aura http://purl.obolibrary.org/obo/MONDO_0005475 GCST90043743 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neck/shoulder pain for three months (UKB data field 3404) 71,764 European ancestry cases, 31,984 European ancestry controls NA NR [11842647] (imputed) 0 Shoulder pain http://purl.obolibrary.org/obo/HP_0030834 GCST90043744 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Migraine (PheCode 340) 1,488 European ancestry cases, 454,860 European ancestry controls NA NR [11842647] (imputed) 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90043745 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hip pain for three months (UKB data field 3414) 39,730 European ancestry cases, 11,212 European ancestry controls NA NR [11842647] (imputed) 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90043746 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other demyelinating diseases of central nervous system (PheCode 341) 222 European ancestry cases, 456,126 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the nervous system http://purl.obolibrary.org/obo/HP_0000707 GCST90043747 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemiplegia (PheCode 342) 448 European ancestry cases, 455,900 European ancestry controls NA NR [11842647] (imputed) 0 hemiplegia, Hemiparesis http://www.ebi.ac.uk/efo/EFO_0009453, http://purl.obolibrary.org/obo/HP_0001269 GCST90043748 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of tobacco currently smoked: Manufactured cigarettes (UKB data field 3446_1) 24,545 European ancestry cases, 10,880 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90043749 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of tobacco currently smoked: Hand-rolled cigarettes (UKB data field 3446_2) 8,370 European ancestry cases, 27,055 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90043750 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of tobacco currently smoked: Cigars or pipes (UKB data field 3446_3) 2,510 European ancestry cases, 32,915 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90043751 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other paralytic syndromes (PheCode 344) 260 European ancestry cases, 456,088 European ancestry controls NA NR [11842647] (imputed) 0 quadriplegia, paraplegia http://www.ebi.ac.uk/efo/EFO_0009684, http://www.ebi.ac.uk/efo/EFO_0009679 GCST90043752 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Generalized convulsive epilepsy (PheCode 345.11) 290 European ancestry cases, 456,058 European ancestry controls NA NR [11842647] (imputed) 0 generalised epilepsy http://www.ebi.ac.uk/efo/EFO_0005917 GCST90043753 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Partial epilepsy (PheCode 345.12) 151 European ancestry cases, 456,197 European ancestry controls NA NR [11842647] (imputed) 0 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90043754 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Epilepsy (PheCode 345.1) 180 European ancestry cases, 456,168 European ancestry controls NA NR [11842647] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90043755 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - diltiazem (UKB data field 20003_1140879806) 918 European ancestry cases, 455,358 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042196 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - metoprolol (UKB data field 20003_1140879818) 870 European ancestry cases, 455,406 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042197 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - propranolol (UKB data field 20003_1140879842) 3,026 European ancestry cases, 453,250 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042198 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sotalol (UKB data field 20003_1140879854) 706 European ancestry cases, 455,570 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042199 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - timolol (UKB data field 20003_1140879866) 332 European ancestry cases, 455,944 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042200 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - atorvastatin (UKB data field 20003_1141146234) 13,604 European ancestry cases, 442,672 European ancestry controls NA NR [11842647] (imputed) 3 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042376 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fexofenadine (UKB data field 20003_1141146428) 1,417 European ancestry cases, 454,859 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042377 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nasacort 55micrograms aqueous nasal spray (UKB data field 20003_1141146508) 200 European ancestry cases, 456,076 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042378 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcium carbonate+cholecalciferol 1.25g/200iu tablet (UKB data field 20003_1141146606) 700 European ancestry cases, 455,576 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042379 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calceos chewable tablet (UKB data field 20003_1141146612) 245 European ancestry cases, 456,031 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042380 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zolmitriptan (UKB data field 20003_1141150620) 400 European ancestry cases, 455,876 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042381 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zomig 2.5mg tablet (UKB data field 20003_1141150624) 424 European ancestry cases, 455,852 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042382 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - brimonidine tartrate (UKB data field 20003_1141150750) 116 European ancestry cases, 456,160 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042383 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nasonex 0.05% aqueous nasal spray (UKB data field 20003_1141150944) 2,282 European ancestry cases, 453,994 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042384 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - losartan potassium+hydrochlorothiazide 50mg/12.5mg tablet (UKB data field 20003_1141151016) 358 European ancestry cases, 455,918 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042385 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cozaar-comp 50mg/12.5mg tablet (UKB data field 20003_1141151018) 118 European ancestry cases, 456,158 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042386 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - naratriptan (UKB data field 20003_1141151284) 334 European ancestry cases, 455,942 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042387 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - naramig 2.5mg tablet (UKB data field 20003_1141151288) 318 European ancestry cases, 455,958 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042388 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - evorel conti patch (UKB data field 20003_1141151718) 516 European ancestry cases, 246,992 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042389 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cipramil 10mg tablet (UKB data field 20003_1141151946) 154 European ancestry cases, 456,122 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042390 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - glimepiride (UKB data field 20003_1141152590) 381 European ancestry cases, 455,895 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042391 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mirtazapine (UKB data field 20003_1141152732) 1,221 European ancestry cases, 455,055 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042392 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - quetiapine (UKB data field 20003_1141152848) 255 European ancestry cases, 456,021 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042393 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - irbesartan (UKB data field 20003_1141152998) 3,219 European ancestry cases, 453,057 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042394 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - aprovel 75mg tablet (UKB data field 20003_1141153006) 375 European ancestry cases, 455,901 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042395 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lercanidipine (UKB data field 20003_1141153026) 1,093 European ancestry cases, 455,183 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042396 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zanidip 10mg tablet (UKB data field 20003_1141153032) 196 European ancestry cases, 456,080 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042397 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - balsalazide disodium (UKB data field 20003_1141153242) 126 European ancestry cases, 456,150 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042398 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - elleste duet conti tablet (UKB data field 20003_1141156644) 923 European ancestry cases, 246,585 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042399 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - candesartan cilexetil (UKB data field 20003_1141156836) 4,846 European ancestry cases, 451,430 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042400 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salbutamol 100micrograms spacehaler (UKB data field 20003_1140926606) 2,858 European ancestry cases, 453,418 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042351 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - meloxicam (UKB data field 20003_1140926732) 1,293 European ancestry cases, 454,983 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042352 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - adizem-xl plus m/r capsule (UKB data field 20003_1140926780) 330 European ancestry cases, 455,946 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042353 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - antihistamine 60mg tablet (UKB data field 20003_1140926922) 328 European ancestry cases, 455,948 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042354 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tamsulosin (UKB data field 20003_1140926934) 3,703 European ancestry cases, 205,065 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042355 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - flomax mr 400micrograms m/r capsule (UKB data field 20003_1140926940) 183 European ancestry cases, 208,585 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042356 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - arthrotec 50 tablet (UKB data field 20003_1140927086) 396 European ancestry cases, 455,880 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042357 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dermol 500 lotion (UKB data field 20003_1140927320) 129 European ancestry cases, 456,147 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042358 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - terbinafine (UKB data field 20003_1140927328) 864 European ancestry cases, 455,412 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042359 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - epaderm ointment (UKB data field 20003_1140927730) 278 European ancestry cases, 455,998 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042360 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zimovane ls 3.75mg tablet (UKB data field 20003_1140928004) 148 European ancestry cases, 456,128 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042361 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ropinirole (UKB data field 20003_1140928274) 308 European ancestry cases, 455,968 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042362 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - moxonidine (UKB data field 20003_1140928284) 390 European ancestry cases, 455,886 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042363 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zumenon 1mg tablet (UKB data field 20003_1140928878) 148 European ancestry cases, 247,360 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042364 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - olanzapine (UKB data field 20003_1140928916) 502 European ancestry cases, 455,774 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042365 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pantoprazole (UKB data field 20003_1140929012) 807 European ancestry cases, 455,469 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042366 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nitromin 400micrograms cfc-free spray (UKB data field 20003_1141145630) 121 European ancestry cases, 456,155 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042367 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nasobec aqueous 50micrograms nasal spray (UKB data field 20003_1141145638) 194 European ancestry cases, 456,082 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042368 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - valsartan (UKB data field 20003_1141145660) 2,143 European ancestry cases, 454,133 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042369 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - diovan 40mg capsule (UKB data field 20003_1141145668) 442 European ancestry cases, 455,834 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042370 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - minerals - magnesium (UKB data field 20003_1141145812) 1,003 European ancestry cases, 455,273 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042371 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - letrozole (UKB data field 20003_1141145896) 278 European ancestry cases, 247,230 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042372 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lipitor 10mg tablet (UKB data field 20003_1141146138) 3,258 European ancestry cases, 453,018 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042373 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - latanoprost (UKB data field 20003_1141146188) 887 European ancestry cases, 455,389 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042374 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - xalatan 0.005% eye drops (UKB data field 20003_1141146198) 1,252 European ancestry cases, 455,024 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042375 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - leflunomide (UKB data field 20003_1141166294) 189 European ancestry cases, 456,087 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042426 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oestrogel 0.06% gel (UKB data field 20003_1141167206) 119 European ancestry cases, 247,389 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042427 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - colofac-100 tablet (UKB data field 20003_1141167334) 562 European ancestry cases, 455,714 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042428 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - qvar 50 inhaler (UKB data field 20003_1141167594) 1,680 European ancestry cases, 454,596 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042429 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - beclomist 50micrograms nasal spray (UKB data field 20003_1141167708) 143 European ancestry cases, 456,133 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042430 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - asasantin retard m/r capsule (UKB data field 20003_1141167848) 115 European ancestry cases, 456,161 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042431 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rizatriptan (UKB data field 20003_1141167932) 355 European ancestry cases, 455,921 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042432 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - maxalt 5mg tablet (UKB data field 20003_1141167940) 228 European ancestry cases, 456,048 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042433 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - isotard 25xl m/r tablet (UKB data field 20003_1141168108) 182 European ancestry cases, 456,094 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042434 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - solpadol capsule (UKB data field 20003_1141168122) 252 European ancestry cases, 456,024 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042435 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clopidogrel (UKB data field 20003_1141168318) 2,920 European ancestry cases, 453,356 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042436 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - plavix 75mg tablet (UKB data field 20003_1141168322) 208 European ancestry cases, 456,068 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042437 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - kliovance 1mg/0.5mg tablet (UKB data field 20003_1141168326) 947 European ancestry cases, 246,561 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042438 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - migraleve tablet (UKB data field 20003_1141168554) 600 European ancestry cases, 455,676 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042439 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - raloxifene hydrochloride (UKB data field 20003_1141168574) 293 European ancestry cases, 247,215 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042440 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - evista 60mg tablet (UKB data field 20003_1141168578) 129 European ancestry cases, 247,379 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042441 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rabeprazole sodium (UKB data field 20003_1141168584) 824 European ancestry cases, 455,452 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042442 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pariet 10mg e/c tablet (UKB data field 20003_1141168590) 278 European ancestry cases, 455,998 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042443 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - solpadeine capsule (UKB data field 20003_1141168650) 119 European ancestry cases, 456,157 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042444 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - orlistat (UKB data field 20003_1141168680) 522 European ancestry cases, 455,754 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042445 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - xenical 120mg capsule (UKB data field 20003_1141168684) 407 European ancestry cases, 455,869 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042446 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - peptac liquid (UKB data field 20003_1141168752) 406 European ancestry cases, 455,870 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042447 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sildenafil (UKB data field 20003_1141168936) 836 European ancestry cases, 455,440 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042448 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - viagra 25mg tablet (UKB data field 20003_1141168944) 132 European ancestry cases, 208,636 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042449 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - viagra 50mg tablet (UKB data field 20003_1141168946) 153 European ancestry cases, 208,615 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042450 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - viagra 100mg tablet (UKB data field 20003_1141168948) 140 European ancestry cases, 208,628 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042451 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cosopt 2%/0.5% eye drops (UKB data field 20003_1141169520) 394 European ancestry cases, 455,882 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042452 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dexamethasone+hypromellose 0.1%/0.5% eye drops (UKB data field 20003_1141169844) 174 European ancestry cases, 456,102 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042453 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oxycodone hydrochloride (UKB data field 20003_1141171038) 103 European ancestry cases, 456,173 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042454 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - exemestane (UKB data field 20003_1141171100) 187 European ancestry cases, 247,321 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042455 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cardicor 1.25mg tablet (UKB data field 20003_1141171152) 409 European ancestry cases, 455,867 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042456 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - eprosartan (UKB data field 20003_1141171336) 263 European ancestry cases, 456,013 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042457 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - trospium (UKB data field 20003_1141171496) 201 European ancestry cases, 456,075 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042458 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pioglitazone (UKB data field 20003_1141171646) 917 European ancestry cases, 455,359 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042459 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - levetiracetam (UKB data field 20003_1141171932) 193 European ancestry cases, 456,083 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042460 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - keppra 250mg tablet (UKB data field 20003_1141171940) 136 European ancestry cases, 456,140 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042461 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - adcal 600mg chewable tablet (UKB data field 20003_1141171948) 1,346 European ancestry cases, 454,930 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042462 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - indivina 1mg/2.5mg tablet (UKB data field 20003_1141172436) 138 European ancestry cases, 247,370 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042463 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - micardis 20mg tablet (UKB data field 20003_1141172492) 127 European ancestry cases, 456,149 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042464 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - irbesartan+hydrochlorothiazide 150mg/12.5mg tablet (UKB data field 20003_1141172682) 102 European ancestry cases, 456,174 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042465 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - coaprovel 150mg/12.5mg tablet (UKB data field 20003_1141172686) 120 European ancestry cases, 456,156 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042466 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - monomax xl 60mg m/r tablet (UKB data field 20003_1141172698) 127 European ancestry cases, 456,149 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042467 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - depakote 250mg e/c tablet (UKB data field 20003_1141172838) 126 European ancestry cases, 456,150 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042468 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - celluvisc 1% single-use eye drops (UKB data field 20003_1141172918) 333 European ancestry cases, 455,943 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042469 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - desloratadine (UKB data field 20003_1141172924) 588 European ancestry cases, 455,688 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042470 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - neoclarityn 5mg tablet (UKB data field 20003_1141172928) 514 European ancestry cases, 455,762 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042471 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ursodeoxycholic acid (UKB data field 20003_1141173328) 141 European ancestry cases, 456,135 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042472 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hydroxocobalamin (UKB data field 20003_1141173348) 374 European ancestry cases, 455,902 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042473 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - doublebase gel (UKB data field 20003_1141174032) 230 European ancestry cases, 456,046 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042474 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - reductil 10mg capsule (UKB data field 20003_1141174508) 132 European ancestry cases, 456,144 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042475 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amias 2mg tablet (UKB data field 20003_1141156846) 475 European ancestry cases, 455,801 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042401 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - montelukast product (UKB data field 20003_1141157126) 810 European ancestry cases, 455,466 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042402 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - singulair 10mg tablet (UKB data field 20003_1141157132) 326 European ancestry cases, 455,950 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042403 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - senna product (UKB data field 20003_1141157178) 149 European ancestry cases, 456,127 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042404 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - glyceryl trinitrate product (UKB data field 20003_1141157252) 418 European ancestry cases, 455,858 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042405 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salmeterol product (UKB data field 20003_1141157264) 274 European ancestry cases, 456,002 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042406 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hydrocortisone product (UKB data field 20003_1141157294) 306 European ancestry cases, 455,970 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042407 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - loratadine product (UKB data field 20003_1141157324) 105 European ancestry cases, 456,171 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042408 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - prednisolone product (UKB data field 20003_1141157402) 159 European ancestry cases, 456,117 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042409 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - budesonide product (UKB data field 20003_1141157418) 129 European ancestry cases, 456,147 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042410 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hypromellose product (UKB data field 20003_1141157458) 245 European ancestry cases, 456,031 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042411 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salbutamol product (UKB data field 20003_1141157486) 703 European ancestry cases, 455,573 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042412 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ispaghula husk product (UKB data field 20003_1141157494) 138 European ancestry cases, 456,138 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042413 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tolterodine l-tartrate (UKB data field 20003_1141162764) 885 European ancestry cases, 455,391 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042414 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - detrusitol 1mg tablet (UKB data field 20003_1141162824) 694 European ancestry cases, 455,582 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042415 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pramipexole (UKB data field 20003_1141164060) 189 European ancestry cases, 456,087 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042416 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mirapexin 0.088mg tablet (UKB data field 20003_1141164068) 120 European ancestry cases, 456,156 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042417 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - salmeterol+fluticasone propionate (UKB data field 20003_1141164086) 818 European ancestry cases, 455,458 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042418 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nebivolol (UKB data field 20003_1141164276) 348 European ancestry cases, 455,928 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042419 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - protium 20mg e/c tablet (UKB data field 20003_1141164616) 107 European ancestry cases, 456,169 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042420 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - adcal-d3 1.5g/10micrograms chewable tablet (UKB data field 20003_1141164828) 3,071 European ancestry cases, 453,205 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042421 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sinemet-62.5 tablet (UKB data field 20003_1141164872) 144 European ancestry cases, 456,132 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042422 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - telmisartan (UKB data field 20003_1141166006) 707 European ancestry cases, 455,569 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042423 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rennie duo oral suspension (UKB data field 20003_1141166086) 149 European ancestry cases, 456,127 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042424 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - implanon 68mg subdermal implant (UKB data field 20003_1141166200) 158 European ancestry cases, 247,350 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042425 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - symbicort 100/6 turbohaler (UKB data field 20003_1141174520) 2,777 European ancestry cases, 453,499 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042476 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - risedronate sodium (UKB data field 20003_1141175684) 903 European ancestry cases, 455,373 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042477 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - actonel 5mg tablet (UKB data field 20003_1141175690) 376 European ancestry cases, 455,900 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042478 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - brinzolamide (UKB data field 20003_1141176284) 156 European ancestry cases, 456,120 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042479 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - azopt 10mg/ml eye drops (UKB data field 20003_1141176288) 189 European ancestry cases, 456,087 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042480 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fosamax 5mg tablet (UKB data field 20003_1141176570) 567 European ancestry cases, 455,709 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042481 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - celecoxib (UKB data field 20003_1141176662) 471 European ancestry cases, 455,805 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042482 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - celebrex 100mg capsule (UKB data field 20003_1141176668) 368 European ancestry cases, 455,908 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042483 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - celebrex 200mg capsule (UKB data field 20003_1141176670) 176 European ancestry cases, 456,100 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042484 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - carbomers (UKB data field 20003_1141176732) 343 European ancestry cases, 455,933 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042485 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - seretide 50 evohaler (UKB data field 20003_1141176832) 5,365 European ancestry cases, 450,911 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042486 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - esomeprazole (UKB data field 20003_1141177526) 1,520 European ancestry cases, 454,756 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042487 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nexium 20mg tablet (UKB data field 20003_1141177532) 786 European ancestry cases, 455,490 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042488 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rosiglitazone (UKB data field 20003_1141177600) 643 European ancestry cases, 455,633 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042489 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - eltroxin 25micrograms tablet (UKB data field 20003_1141178036) 111 European ancestry cases, 456,165 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042490 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zapain caplet (UKB data field 20003_1141178052) 155 European ancestry cases, 456,121 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042491 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tenofovir (UKB data field 20003_1141179764) 122 European ancestry cases, 456,154 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042492 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bimatoprost (UKB data field 20003_1141179914) 254 European ancestry cases, 456,022 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042493 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lumigan 0.3mg/ml eye drops (UKB data field 20003_1141179920) 287 European ancestry cases, 455,989 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042494 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cozaar 25mg tablet (UKB data field 20003_1141179974) 504 European ancestry cases, 455,772 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042495 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dovobet ointment (UKB data field 20003_1141179992) 523 European ancestry cases, 455,753 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042496 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fybogel orange s/f granules (UKB data field 20003_1141180036) 929 European ancestry cases, 455,347 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042497 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - etoricoxib (UKB data field 20003_1141180140) 396 European ancestry cases, 455,880 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042498 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - arcoxia 60mg tablet (UKB data field 20003_1141180148) 169 European ancestry cases, 456,107 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042499 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - arcoxia 90mg tablet (UKB data field 20003_1141180150) 119 European ancestry cases, 456,157 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042500 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic sinusitis (PheCode 475) 1,568 European ancestry cases, 454,780 European ancestry controls NA NR [11842647] (imputed) 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90044054 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Epistaxis or throat hemorrhage (PheCode 477) 2,103 European ancestry cases, 454,245 European ancestry controls NA NR [11842647] (imputed) 0 epistaxis http://www.ebi.ac.uk/efo/EFO_0003895 GCST90044055 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Throat pain (PheCode 478) 323 European ancestry cases, 456,025 European ancestry controls NA NR [11842647] (imputed) 0 throat disease http://www.ebi.ac.uk/efo/EFO_0009479 GCST90044056 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cochlear implant (UKB data field 4792) 135 European ancestry cases, 150,375 European ancestry controls NA NR [11842647] (imputed) 0 cochlear implant http://www.ebi.ac.uk/efo/EFO_0009728 GCST90044057 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other upper respiratory disease (PheCode 479) 2,696 European ancestry cases, 453,652 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90044058 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pneumococcal pneumonia (PheCode 480.11) 4,465 European ancestry cases, 451,883 European ancestry controls NA NR [11842647] (imputed) 0 pneumococcal infection http://www.ebi.ac.uk/efo/EFO_0000772 GCST90044059 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bacterial pneumonia (PheCode 480.1) 434 European ancestry cases, 455,914 European ancestry controls NA NR [11842647] (imputed) 0 typhus http://www.ebi.ac.uk/efo/EFO_0009117 GCST90044060 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bronchopneumonia and lung abscess (PheCode 480.5) 297 European ancestry cases, 456,051 European ancestry controls NA NR [11842647] (imputed) 0 Lung Abscess, bronchopneumonia http://www.ebi.ac.uk/efo/EFO_1001362, http://www.ebi.ac.uk/efo/EFO_0007184 GCST90044061 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tinnitus: No, never (UKB data field 4803_0) 104,711 European ancestry cases, 43,078 European ancestry controls NA NR [11842647] (imputed) 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90044062 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tinnitus: Yes, now most or all of the time (UKB data field 4803_11) 9,697 European ancestry cases, 138,092 European ancestry controls NA NR [11842647] (imputed) 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90044063 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tinnitus: Yes, now a lot of the time (UKB data field 4803_12) 3,737 European ancestry cases, 144,052 European ancestry controls NA NR [11842647] (imputed) 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90044064 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tinnitus: Yes, now some of the time (UKB data field 4803_13) 13,154 European ancestry cases, 134,635 European ancestry controls NA NR [11842647] (imputed) 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90044065 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tinnitus: Yes, but not now, but have in the past (UKB data field 4803_14) 16,490 European ancestry cases, 131,299 European ancestry controls NA NR [11842647] (imputed) 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90044066 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pneumonia (PheCode 480) 2,842 European ancestry cases, 453,506 European ancestry controls NA NR [11842647] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90044067 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Influenza (PheCode 481) 248 European ancestry cases, 456,100 European ancestry controls NA NR [11842647] (imputed) 0 influenza http://www.ebi.ac.uk/efo/EFO_0007328 GCST90044068 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute bronchitis and bronchiolitis (PheCode 483) 172 European ancestry cases, 456,176 European ancestry controls NA NR [11842647] (imputed) 0 Acute bronchitis http://purl.obolibrary.org/obo/HP_0012388 GCST90044069 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Attempted fluid intelligence (FI) test. (UKB data field 4924) 1,942 European ancestry cases, 146,808 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90044070 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Asthma with exacerbation (PheCode 495.2) 254 European ancestry cases, 456,094 European ancestry controls NA NR [11842647] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90044071 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Asthma (PheCode 495) 2,365 European ancestry cases, 453,983 European ancestry controls NA NR [11842647] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90044072 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Emphysema (PheCode 496.1) 203 European ancestry cases, 456,145 European ancestry controls NA NR [11842647] (imputed) 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90044073 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Obstructive chronic bronchitis (PheCode 496.21) 2,115 European ancestry cases, 454,233 European ancestry controls NA NR [11842647] (imputed) 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90044074 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bronchiectasis (PheCode 496.3) 583 European ancestry cases, 455,765 European ancestry controls NA NR [11842647] (imputed) 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90044075 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic airway obstruction (PheCode 496) 389 European ancestry cases, 455,959 European ancestry controls NA NR [11842647] (imputed) 0 Airway obstruction http://purl.obolibrary.org/obo/HP_0006536 GCST90044076 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bronchitis (PheCode 497) 229 European ancestry cases, 456,119 European ancestry controls NA NR [11842647] (imputed) 0 bronchial disease http://www.ebi.ac.uk/efo/EFO_1002018 GCST90044077 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pneumonitis due to inhalation of food or vomitus (PheCode 501) 232 European ancestry cases, 456,116 European ancestry controls NA NR [11842647] (imputed) 0 pneumonitis http://www.ebi.ac.uk/efo/EFO_1001991 GCST90044078 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ulcerative colitis (chronic) (PheCode 555.21) 507 European ancestry cases, 455,841 European ancestry controls NA NR [11842647] (imputed) 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90044154 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ulcerative colitis (PheCode 555.2) 2,569 European ancestry cases, 453,779 European ancestry controls NA NR [11842647] (imputed) 1 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90044155 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ulceration of intestine (PheCode 556.1) 301 European ancestry cases, 456,047 European ancestry controls NA NR [11842647] (imputed) 0 gastrointestinal disease http://www.ebi.ac.uk/efo/EFO_0010282 GCST90044156 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ulceration of the lower GI tract (PheCode 556) 235 European ancestry cases, 456,113 European ancestry controls NA NR [11842647] (imputed) 0 gastrointestinal disease http://www.ebi.ac.uk/efo/EFO_0010282 GCST90044157 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Celiac disease (PheCode 557.1) 1,036 European ancestry cases, 455,312 European ancestry controls NA NR [11842647] (imputed) 2 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90044158 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Intestinal malabsorption (non-celiac) (PheCode 557) 150 European ancestry cases, 456,198 European ancestry controls NA NR [11842647] (imputed) 0 lactose intolerance http://www.ebi.ac.uk/efo/EFO_1000062 GCST90044159 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Noninfectious gastroenteritis (PheCode 558) 11,373 European ancestry cases, 444,975 European ancestry controls NA NR [11842647] (imputed) 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90044160 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ileostomy status (PheCode 559) 863 European ancestry cases, 455,485 European ancestry controls NA NR [11842647] (imputed) 0 ileostomy http://www.ebi.ac.uk/efo/EFO_0010681 GCST90044161 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Impaction of intestine (PheCode 560.2) 146 European ancestry cases, 456,202 European ancestry controls NA NR [11842647] (imputed) 0 gastrointestinal disease http://www.ebi.ac.uk/efo/EFO_0010282 GCST90044162 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peritoneal or intestinal adhesions (PheCode 560.3) 807 European ancestry cases, 455,541 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the gastrointestinal tract http://purl.obolibrary.org/obo/HP_0011024 GCST90044163 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other intestinal obstruction (PheCode 560.4) 2,417 European ancestry cases, 453,931 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the gastrointestinal tract http://purl.obolibrary.org/obo/HP_0011024 GCST90044164 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diarrhea (PheCode 561.1) 367 European ancestry cases, 455,981 European ancestry controls NA NR [11842647] (imputed) 0 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST90044165 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Flatulence (PheCode 561.2) 424 European ancestry cases, 455,924 European ancestry controls NA NR [11842647] (imputed) 0 flatulence http://www.ebi.ac.uk/efo/EFO_0009669 GCST90044166 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by presbyopia: Right eye (UKB data field 5610_1) 2,143 European ancestry cases, 36,937 European ancestry controls NA NR [11842647] (imputed) 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90044167 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by presbyopia: Left eye (UKB data field 5610_2) 2,170 European ancestry cases, 36,910 European ancestry controls NA NR [11842647] (imputed) 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90044168 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by presbyopia: Both eyes (UKB data field 5610_3) 34,767 European ancestry cases, 4,313 European ancestry controls NA NR [11842647] (imputed) 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90044169 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms involving digestive system (PheCode 561) 10,886 European ancestry cases, 445,462 European ancestry controls NA NR [11842647] (imputed) 0 fecal incontinence http://www.ebi.ac.uk/efo/EFO_0009523 GCST90044170 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diverticulosis (PheCode 562.1) 16,743 European ancestry cases, 439,605 European ancestry controls NA NR [11842647] (imputed) 0 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90044171 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Constipation (PheCode 563) 4,781 European ancestry cases, 451,567 European ancestry controls NA NR [11842647] (imputed) 0 Constipation http://purl.obolibrary.org/obo/HP_0002019 GCST90044172 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Irritable Bowel Syndrome (PheCode 564.1) 1,480 European ancestry cases, 454,868 European ancestry controls NA NR [11842647] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90044173 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal findings on exam of gastrointestinal tract/ abdominal area (PheCode 564.8) 1,135 European ancestry cases, 455,213 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the abdominal organs http://purl.obolibrary.org/obo/HP_0002012 GCST90044174 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Personal history of diseases of digestive system (PheCode 564.9) 197 European ancestry cases, 456,151 European ancestry controls NA NR [11842647] (imputed) 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90044175 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Functional digestive disorders (PheCode 564) 512 European ancestry cases, 455,836 European ancestry controls NA NR [11842647] (imputed) 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90044176 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anal and rectal polyp (PheCode 565.1) 5,167 European ancestry cases, 451,181 European ancestry controls NA NR [11842647] (imputed) 0 polyp http://www.ebi.ac.uk/efo/EFO_0000662 GCST90044177 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anal and rectal conditions (PheCode 565) 6,784 European ancestry cases, 449,564 European ancestry controls NA NR [11842647] (imputed) 0 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90044178 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Postinflammatory pulmonary fibrosis (PheCode 502) 363 European ancestry cases, 455,985 European ancestry controls NA NR [11842647] (imputed) 0 pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0009448 GCST90044079 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pulmonary congestion and hypostasis (PheCode 503) 101 European ancestry cases, 456,247 European ancestry controls NA NR [11842647] (imputed) 0 pulmonary vascular congestion http://www.ebi.ac.uk/efo/EFO_0009866 GCST90044080 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other alveolar and parietoalveolar pneumonopathy (PheCode 504) 179 European ancestry cases, 456,169 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90044081 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Empyema and pneumothorax (PheCode 506) 637 European ancestry cases, 455,711 European ancestry controls NA NR [11842647] (imputed) 0 pleural empyema http://www.ebi.ac.uk/efo/EFO_0009680 GCST90044082 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pleurisy; pleural effusion (PheCode 507) 1,934 European ancestry cases, 454,414 European ancestry controls NA NR [11842647] (imputed) 0 pleural effusion http://www.ebi.ac.uk/efo/EFO_0009637 GCST90044083 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pulmonary collapse; interstitial and compensatory emphysema (PheCode 508) 185 European ancestry cases, 456,163 European ancestry controls NA NR [11842647] (imputed) 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90044084 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Respiratory failure (PheCode 509.1) 312 European ancestry cases, 456,036 European ancestry controls NA NR [11842647] (imputed) 0 respiratory failure http://www.ebi.ac.uk/efo/EFO_0009686 GCST90044085 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Respiratory insufficiency (PheCode 509.2) 241 European ancestry cases, 456,107 European ancestry controls NA NR [11842647] (imputed) 0 Respiratory insufficiency http://purl.obolibrary.org/obo/HP_0002093 GCST90044086 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other diseases of lung (PheCode 510) 322 European ancestry cases, 456,026 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90044087 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Painful respiration (PheCode 512.2) 190 European ancestry cases, 456,158 European ancestry controls NA NR [11842647] (imputed) 0 irregular respiration http://www.ebi.ac.uk/efo/EFO_0009841 GCST90044088 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Shortness of breath (PheCode 512.7) 3,104 European ancestry cases, 453,244 European ancestry controls NA NR [11842647] (imputed) 0 shortness of breath http://www.ebi.ac.uk/efo/EFO_0009727 GCST90044089 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cough (PheCode 512.8) 1,286 European ancestry cases, 455,062 European ancestry controls NA NR [11842647] (imputed) 0 Cough http://purl.obolibrary.org/obo/HP_0012735 GCST90044090 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other dyspnea (PheCode 512.9) 577 European ancestry cases, 455,771 European ancestry controls NA NR [11842647] (imputed) 0 Dyspnea http://purl.obolibrary.org/obo/HP_0002094 GCST90044091 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hyperventilation (PheCode 513.4) 139 European ancestry cases, 456,209 European ancestry controls NA NR [11842647] (imputed) 0 Hyperventilation http://purl.obolibrary.org/obo/HP_0002883 GCST90044092 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal findings examination of lungs (PheCode 514) 1,511 European ancestry cases, 454,837 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal lung morphology http://purl.obolibrary.org/obo/HP_0002088 GCST90044093 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemoptysis (PheCode 516.1) 1,684 European ancestry cases, 454,664 European ancestry controls NA NR [11842647] (imputed) 0 Hemoptysis http://purl.obolibrary.org/obo/HP_0002105 GCST90044094 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other diseases of respiratory system, NEC (PheCode 519.8) 4,719 European ancestry cases, 451,629 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044095 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms involving respiratory system and other chest symptoms (PheCode 519.9) 232 European ancestry cases, 456,116 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90044096 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disturbances in tooth eruption (PheCode 520.2) 1,965 European ancestry cases, 454,383 European ancestry controls NA NR [11842647] (imputed) 0 Impacted tooth http://purl.obolibrary.org/obo/HP_0011079 GCST90044097 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dental caries (PheCode 521.1) 2,906 European ancestry cases, 453,442 European ancestry controls NA NR [11842647] (imputed) 0 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST90044098 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Periapical abscess (PheCode 522.5) 1,026 European ancestry cases, 455,322 European ancestry controls NA NR [11842647] (imputed) 0 abscess http://www.ebi.ac.uk/efo/EFO_0003030 GCST90044099 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of pulp and periapical tissues (PheCode 522) 532 European ancestry cases, 455,816 European ancestry controls NA NR [11842647] (imputed) 0 dental pulp disease http://www.ebi.ac.uk/efo/EFO_0009540 GCST90044100 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute periodontitis (PheCode 523.31) 128 European ancestry cases, 456,220 European ancestry controls NA NR [11842647] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90044101 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic periodontitis (PheCode 523.32) 950 European ancestry cases, 455,398 European ancestry controls NA NR [11842647] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90044102 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gingival and periodontal diseases (PheCode 523) 376 European ancestry cases, 455,972 European ancestry controls NA NR [11842647] (imputed) 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90044103 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Anomalies of tooth position/malocclusion (PheCode 524.3) 257 European ancestry cases, 456,091 European ancestry controls NA NR [11842647] (imputed) 0 Dental malocclusion http://purl.obolibrary.org/obo/HP_0000689 GCST90044104 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other diseases of the teeth and supporting structures (PheCode 525) 2,396 European ancestry cases, 453,952 European ancestry controls NA NR [11842647] (imputed) 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90044105 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cysts of the jaws (PheCode 526.1) 274 European ancestry cases, 456,074 European ancestry controls NA NR [11842647] (imputed) 0 Odontogenic Cyst http://www.ebi.ac.uk/efo/EFO_1000406 GCST90044106 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Temporomandibular joint disorder, unspecified (PheCode 526.41) 217 European ancestry cases, 456,131 European ancestry controls NA NR [11842647] (imputed) 0 temporomandibular joint disorder http://www.ebi.ac.uk/efo/EFO_0005279 GCST90044107 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Jaw disease, not otherwise specified (PheCode 526.9) 176 European ancestry cases, 456,172 European ancestry controls NA NR [11842647] (imputed) 0 jaw disease http://www.ebi.ac.uk/efo/EFO_0009468 GCST90044108 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sialoadenitis (PheCode 527.2) 350 European ancestry cases, 455,998 European ancestry controls NA NR [11842647] (imputed) 0 sialadenitis http://www.ebi.ac.uk/efo/EFO_1001179 GCST90044109 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other specified diseases of the salivary glands (PheCode 527.8) 113 European ancestry cases, 456,235 European ancestry controls NA NR [11842647] (imputed) 0 salivary gland disease http://www.ebi.ac.uk/efo/EFO_0008581 GCST90044110 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Stomatitis and mucositis (ulcerative) (PheCode 528.11) 165 European ancestry cases, 456,183 European ancestry controls NA NR [11842647] (imputed) 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90044111 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cellulitis and abscess of oral soft tissues (PheCode 528.3) 151 European ancestry cases, 456,197 European ancestry controls NA NR [11842647] (imputed) 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90044112 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cyst of the salivary gland (PheCode 528.41) 99 European ancestry cases, 456,249 European ancestry controls NA NR [11842647] (imputed) 0 salivary gland disease http://www.ebi.ac.uk/efo/EFO_0008581 GCST90044113 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of lips (PheCode 528.5) 661 European ancestry cases, 455,687 European ancestry controls NA NR [11842647] (imputed) 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90044114 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leukoplakia of oral mucosa (PheCode 528.6) 312 European ancestry cases, 456,036 European ancestry controls NA NR [11842647] (imputed) 0 Oral leukoplakia http://purl.obolibrary.org/obo/HP_0002745 GCST90044115 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sialolithiasis (PheCode 528.7) 291 European ancestry cases, 456,057 European ancestry controls NA NR [11842647] (imputed) 0 sialolithiasis http://www.ebi.ac.uk/efo/EFO_1001180 GCST90044116 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of the oral soft tissues, excluding lesions specific for gingiva and tongue (PheCode 528) 1,923 European ancestry cases, 454,425 European ancestry controls NA NR [11842647] (imputed) 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90044117 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Glossitis (PheCode 529.1) 247 European ancestry cases, 456,101 European ancestry controls NA NR [11842647] (imputed) 0 glossitis http://www.ebi.ac.uk/efo/EFO_1000951 GCST90044118 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases and other conditions of the tongue (PheCode 529) 913 European ancestry cases, 455,435 European ancestry controls NA NR [11842647] (imputed) 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90044119 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. GERD (PheCode 530.11) 14,372 European ancestry cases, 441,976 European ancestry controls NA NR [11842647] (imputed) 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90044120 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ulcer of esophagus (PheCode 530.12) 3,856 European ancestry cases, 452,492 European ancestry controls NA NR [11842647] (imputed) 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90044121 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reflux esophagitis (PheCode 530.14) 8,570 European ancestry cases, 447,778 European ancestry controls NA NR [11842647] (imputed) 0 Esophagitis http://purl.obolibrary.org/obo/HP_0100633 GCST90044122 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Esophagitis, GERD and related diseases (PheCode 530.1) 6,591 European ancestry cases, 449,757 European ancestry controls NA NR [11842647] (imputed) 1 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90044123 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Esophageal bleeding (varices/hemorrhage) (PheCode 530.2) 957 European ancestry cases, 455,391 European ancestry controls NA NR [11842647] (imputed) 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90044124 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Stricture and stenosis of esophagus (PheCode 530.3) 1,217 European ancestry cases, 455,131 European ancestry controls NA NR [11842647] (imputed) 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90044125 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of esophageal motility (PheCode 530.5) 489 European ancestry cases, 455,859 European ancestry controls NA NR [11842647] (imputed) 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90044126 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gastroesophageal laceration-hemorrhage syndrome (PheCode 530.7) 242 European ancestry cases, 456,106 European ancestry controls NA NR [11842647] (imputed) 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90044127 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Heartburn (PheCode 530.9) 1,142 European ancestry cases, 455,206 European ancestry controls NA NR [11842647] (imputed) 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90044128 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Length of longest manic irritable episode - At least two days but less than a week (UKB data field 5663) 5,199 European ancestry cases, 19,523 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044179 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Severity of manic irritable episodes - No problems (UKB data field 5674) 19,406 European ancestry cases, 7,368 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044180 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peritonitis and retroperitoneal infections (PheCode 567) 408 European ancestry cases, 455,940 European ancestry controls NA NR [11842647] (imputed) 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90044181 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peritoneal adhesions (postoperative) (postinfection) (PheCode 568.1) 549 European ancestry cases, 455,799 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the gastrointestinal tract http://purl.obolibrary.org/obo/HP_0011024 GCST90044182 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Toxic gastroenteritis and colitis (PheCode 569.1) 102 European ancestry cases, 456,246 European ancestry controls NA NR [11842647] (imputed) 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90044183 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gastrointestinal complications (PheCode 569.2) 181 European ancestry cases, 456,167 European ancestry controls NA NR [11842647] (imputed) 0 gastrointestinal disease http://www.ebi.ac.uk/efo/EFO_0010282 GCST90044184 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of intestine (PheCode 569) 2,040 European ancestry cases, 454,308 European ancestry controls NA NR [11842647] (imputed) 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90044185 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cirrhosis of liver without mention of alcohol (PheCode 571.51) 240 European ancestry cases, 456,108 European ancestry controls NA NR [11842647] (imputed) 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90044186 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other chronic nonalcoholic liver disease (PheCode 571.5) 334 European ancestry cases, 456,014 European ancestry controls NA NR [11842647] (imputed) 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90044187 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Primary biliary cirrhosis (PheCode 571.6) 121 European ancestry cases, 456,227 European ancestry controls NA NR [11842647] (imputed) 0 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST90044188 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Liver abscess and sequelae of chronic liver disease (PheCode 571.8) 253 European ancestry cases, 456,095 European ancestry controls NA NR [11842647] (imputed) 0 Hepatic failure http://purl.obolibrary.org/obo/HP_0001399 GCST90044189 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ascites (non malignant) (PheCode 572) 470 European ancestry cases, 455,878 European ancestry controls NA NR [11842647] (imputed) 0 Ascites http://purl.obolibrary.org/obo/HP_0001541 GCST90044190 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Jaundice (not of newborn) (PheCode 573.5) 414 European ancestry cases, 455,934 European ancestry controls NA NR [11842647] (imputed) 0 Jaundice http://purl.obolibrary.org/obo/HP_0000952 GCST90044191 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal results of function study of liver (PheCode 573.7) 734 European ancestry cases, 455,614 European ancestry controls NA NR [11842647] (imputed) 0 Abnormality of the liver http://purl.obolibrary.org/obo/HP_0001392 GCST90044192 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of liver (PheCode 573) 396 European ancestry cases, 455,952 European ancestry controls NA NR [11842647] (imputed) 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90044193 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cholelithiasis with acute cholecystitis (PheCode 574.11) 1,559 European ancestry cases, 454,789 European ancestry controls NA NR [11842647] (imputed) 0 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90044194 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cholelithiasis with other cholecystitis (PheCode 574.12) 5,570 European ancestry cases, 450,778 European ancestry controls NA NR [11842647] (imputed) 0 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90044195 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cholelithiasis (PheCode 574.1) 7,426 European ancestry cases, 448,922 European ancestry controls NA NR [11842647] (imputed) 0 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90044196 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Calculus of bile duct (PheCode 574.2) 2,456 European ancestry cases, 453,892 European ancestry controls NA NR [11842647] (imputed) 0 Non-Neoplastic Bile Duct Disorder http://www.ebi.ac.uk/efo/EFO_1000400 GCST90044197 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cholecystitis without cholelithiasis (PheCode 574.3) 2,650 European ancestry cases, 453,698 European ancestry controls NA NR [11842647] (imputed) 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90044198 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cholangitis (PheCode 575.1) 359 European ancestry cases, 455,989 European ancestry controls NA NR [11842647] (imputed) 0 Cholangitis http://purl.obolibrary.org/obo/HP_0030151 GCST90044199 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Obstruction of bile duct (PheCode 575.2) 545 European ancestry cases, 455,803 European ancestry controls NA NR [11842647] (imputed) 0 Non-Neoplastic Bile Duct Disorder http://www.ebi.ac.uk/efo/EFO_1000400 GCST90044200 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of gallbladder (PheCode 575.7) 345 European ancestry cases, 456,003 European ancestry controls NA NR [11842647] (imputed) 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90044201 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of biliary tract (PheCode 575.8) 493 European ancestry cases, 455,855 European ancestry controls NA NR [11842647] (imputed) 0 biliary tract disease http://www.ebi.ac.uk/efo/EFO_0009534 GCST90044202 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nonspecific abnormal findings on radiological and other examination of biliary tract (PheCode 575.9) 104 European ancestry cases, 456,244 European ancestry controls NA NR [11842647] (imputed) 0 biliary tract disease http://www.ebi.ac.uk/efo/EFO_0009534 GCST90044203 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of esophagus (PheCode 530) 355 European ancestry cases, 455,993 European ancestry controls NA NR [11842647] (imputed) 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90044129 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemorrhage from gastrointestinal ulcer (PheCode 531.1) 534 European ancestry cases, 455,814 European ancestry controls NA NR [11842647] (imputed) 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90044130 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gastric ulcer (PheCode 531.2) 2,413 European ancestry cases, 453,935 European ancestry controls NA NR [11842647] (imputed) 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90044131 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Duodenal ulcer (PheCode 531.3) 1,484 European ancestry cases, 454,864 European ancestry controls NA NR [11842647] (imputed) 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90044132 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Peptic ulcer, site unspecified (PheCode 531.4) 118 European ancestry cases, 456,230 European ancestry controls NA NR [11842647] (imputed) 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90044133 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dysphagia (PheCode 532) 4,601 European ancestry cases, 451,747 European ancestry controls NA NR [11842647] (imputed) 0 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST90044134 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute gastritis (PheCode 535.1) 750 European ancestry cases, 455,598 European ancestry controls NA NR [11842647] (imputed) 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90044135 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Atrophic gastritis (PheCode 535.2) 180 European ancestry cases, 456,168 European ancestry controls NA NR [11842647] (imputed) 0 atrophic gastritis http://www.ebi.ac.uk/efo/EFO_1000826 GCST90044136 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Duodenitis (PheCode 535.6) 2,286 European ancestry cases, 454,062 European ancestry controls NA NR [11842647] (imputed) 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90044137 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other specified gastritis (PheCode 535.8) 4,899 European ancestry cases, 451,449 European ancestry controls NA NR [11842647] (imputed) 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90044138 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gastritis and duodenitis (PheCode 535) 17,420 European ancestry cases, 438,928 European ancestry controls NA NR [11842647] (imputed) 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90044139 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of stomach and duodenum (PheCode 537) 1,301 European ancestry cases, 455,047 European ancestry controls NA NR [11842647] (imputed) 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90044140 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute appendicitis (PheCode 540.11) 2,588 European ancestry cases, 453,760 European ancestry controls NA NR [11842647] (imputed) 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90044141 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Appendicitis (PheCode 540.1) 564 European ancestry cases, 455,784 European ancestry controls NA NR [11842647] (imputed) 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90044142 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Appendiceal conditions (PheCode 540) 130 European ancestry cases, 456,218 European ancestry controls NA NR [11842647] (imputed) 0 disorder of appendix http://www.ebi.ac.uk/efo/EFO_0009542 GCST90044143 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) are affected by cataract: Right eye (UKB data field 5441_1) 1,119 European ancestry cases, 4,108 European ancestry controls NA NR [11842647] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90044144 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) are affected by cataract: Left eye (UKB data field 5441_2) 925 European ancestry cases, 4,302 European ancestry controls NA NR [11842647] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90044145 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) are affected by cataract: Both eyes (UKB data field 5441_3) 3,183 European ancestry cases, 2,044 European ancestry controls NA NR [11842647] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90044146 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Inguinal hernia (PheCode 550.1) 16,749 European ancestry cases, 439,599 European ancestry controls NA NR [11842647] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90044147 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diaphragmatic hernia (PheCode 550.2) 10,772 European ancestry cases, 445,576 European ancestry controls NA NR [11842647] (imputed) 0 Hiatus hernia http://purl.obolibrary.org/obo/HP_0002036 GCST90044148 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Femoral hernia (PheCode 550.3) 614 European ancestry cases, 455,734 European ancestry controls NA NR [11842647] (imputed) 0 femoral hernia http://www.ebi.ac.uk/efo/EFO_1001791 GCST90044149 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Umbilical hernia (PheCode 550.4) 3,283 European ancestry cases, 453,065 European ancestry controls NA NR [11842647] (imputed) 0 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90044150 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ventral hernia (PheCode 550.5) 3,092 European ancestry cases, 453,256 European ancestry controls NA NR [11842647] (imputed) 0 ventral hernia http://www.ebi.ac.uk/efo/EFO_1001866 GCST90044151 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abdominal hernia (PheCode 550) 3,327 European ancestry cases, 453,021 European ancestry controls NA NR [11842647] (imputed) 0 Hernia of the abdominal wall http://purl.obolibrary.org/obo/HP_0004299 GCST90044152 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Regional enteritis (PheCode 555.1) 1,342 European ancestry cases, 455,006 European ancestry controls NA NR [11842647] (imputed) 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90044153 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute pancreatitis (PheCode 577.1) 1,748 European ancestry cases, 454,600 European ancestry controls NA NR [11842647] (imputed) 0 acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1000652 GCST90044204 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic pancreatitis (PheCode 577.2) 322 European ancestry cases, 456,026 European ancestry controls NA NR [11842647] (imputed) 0 chronic pancreatitis http://www.ebi.ac.uk/efo/EFO_0000342 GCST90044205 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cyst and pseudocyst of pancreas (PheCode 577.3) 268 European ancestry cases, 456,080 European ancestry controls NA NR [11842647] (imputed) 0 Pancreatic pseudocyst http://purl.obolibrary.org/obo/HP_0005206 GCST90044206 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of pancreas (PheCode 577) 242 European ancestry cases, 456,106 European ancestry controls NA NR [11842647] (imputed) 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90044207 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hematemesis (PheCode 578.1) 1,377 European ancestry cases, 454,971 European ancestry controls NA NR [11842647] (imputed) 0 Hematemesis http://purl.obolibrary.org/obo/HP_0002248 GCST90044208 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Blood in stool (PheCode 578.2) 1,748 European ancestry cases, 454,600 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90044209 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemorrhage of rectum and anus (PheCode 578.8) 10,813 European ancestry cases, 445,535 European ancestry controls NA NR [11842647] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90044210 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemorrhage of gastrointestinal tract (PheCode 578.9) 3,784 European ancestry cases, 452,564 European ancestry controls NA NR [11842647] (imputed) 0 gastrointestinal disease http://www.ebi.ac.uk/efo/EFO_0010282 GCST90044211 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nonspecific abnormal findings in stool contents (PheCode 579.8) 909 European ancestry cases, 455,439 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90044212 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other symptoms involving abdomen and pelvis (PheCode 579) 734 European ancestry cases, 455,614 European ancestry controls NA NR [11842647] (imputed) 0 gastrointestinal disease http://www.ebi.ac.uk/efo/EFO_0010282 GCST90044213 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nephrotic syndrome without mention of glomerulonephritis (PheCode 580.2) 95 European ancestry cases, 456,253 European ancestry controls NA NR [11842647] (imputed) 0 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90044214 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by hypermetropia (long sight): Right eye (UKB data field 5832_1) 1,391 European ancestry cases, 17,339 European ancestry controls NA NR [11842647] (imputed) 0 Hypermetropia http://purl.obolibrary.org/obo/HP_0000540 GCST90044215 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by hypermetropia (long sight): Left eye (UKB data field 5832_2) 1,304 European ancestry cases, 17,426 European ancestry controls NA NR [11842647] (imputed) 0 Hypermetropia http://purl.obolibrary.org/obo/HP_0000540 GCST90044216 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by hypermetropia (long sight): Both eyes (UKB data field 5832_3) 16,035 European ancestry cases, 2,695 European ancestry controls NA NR [11842647] (imputed) 0 Hypermetropia http://purl.obolibrary.org/obo/HP_0000540 GCST90044217 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by myopia (short sight): Right eye (UKB data field 5843_1) 2,053 European ancestry cases, 34,570 European ancestry controls NA NR [11842647] (imputed) 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90044218 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by myopia (short sight): Left eye (UKB data field 5843_2) 1,920 European ancestry cases, 34,703 European ancestry controls NA NR [11842647] (imputed) 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90044219 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by myopia (short sight): Both eyes (UKB data field 5843_3) 32,650 European ancestry cases, 3,973 European ancestry controls NA NR [11842647] (imputed) 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90044220 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute renal failure (PheCode 585.1) 1,199 European ancestry cases, 455,149 European ancestry controls NA NR [11842647] (imputed) 0 acute kidney failure http://purl.obolibrary.org/obo/MONDO_0002492 GCST90044221 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Renal failure, not otherwise specified (PheCode 585.2) 235 European ancestry cases, 456,113 European ancestry controls NA NR [11842647] (imputed) 0 kidney failure http://www.ebi.ac.uk/efo/EFO_1002048 GCST90044222 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic renal failure [CKD] (PheCode 585.3) 562 European ancestry cases, 455,786 European ancestry controls NA NR [11842647] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90044223 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by astigmatism: Right eye (UKB data field 5855_1) 1,793 European ancestry cases, 10,389 European ancestry controls NA NR [11842647] (imputed) 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90044224 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by astigmatism: Left eye (UKB data field 5855_2) 1,959 European ancestry cases, 10,223 European ancestry controls NA NR [11842647] (imputed) 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90044225 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Which eye(s) affected by astigmatism: Both eyes (UKB data field 5855_3) 8,430 European ancestry cases, 3,752 European ancestry controls NA NR [11842647] (imputed) 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90044226 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cyst of kidney, acquired (PheCode 586.2) 148 European ancestry cases, 456,200 European ancestry controls NA NR [11842647] (imputed) 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90044227 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Stricture/obstruction of ureter (PheCode 586.4) 621 European ancestry cases, 455,727 European ancestry controls NA NR [11842647] (imputed) 0 stricture or kinking of ureter http://purl.obolibrary.org/obo/MONDO_0002674 GCST90044228 Genome-wide genotyping array 2022-03-30 35215271 Almandil NB 2022-01-27 Pharmaceuticals (Basel) www.ncbi.nlm.nih.gov/pubmed/35215271 Integration of Transcriptome and Exome Genotyping Identifies Significant Variants with Autism Spectrum Disorder. Autism spectrum disorder 70 Arab ancestry cases, 132 Arab ancestry controls NA Illumina [243345] 31 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST012816 Exome-wide sequencing 2022-04-25 35381062 Kaivola K 2021-10-25 Brain www.ncbi.nlm.nih.gov/pubmed/35381062 Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups. Dementia with Lewy bodies in APOE e4- carriers 1,393 European ancestry cases, 2,271 European ancestry controls NA NR [256446623] 1 Lewy body dementia http://www.ebi.ac.uk/efo/EFO_0006792 GCST90093377 Genome-wide sequencing 2022-04-25 35381062 Kaivola K 2021-10-25 Brain www.ncbi.nlm.nih.gov/pubmed/35381062 Genetic evaluation of dementia with Lewy bodies implicates distinct disease subgroups. Dementia with Lewy bodies in APOE e4+ carriers 1,180 European ancestry cases, 657 European ancestry controls NA NR [256446623] 1 Lewy body dementia http://www.ebi.ac.uk/efo/EFO_0006792 GCST90093378 Genome-wide sequencing 2022-04-20 34836419 Nounu A 2021-11-21 Nutrients www.ncbi.nlm.nih.gov/pubmed/34836419 Salicylic Acid and Risk of Colorectal Cancer: A Two-Sample Mendelian Randomization Study. Salicylic acid levels 14,149 individuals NA Affymetrix [NR] (imputed) 1 salicylic acid measurement http://www.ebi.ac.uk/efo/EFO_0020948 GCST90097055 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Farm workers (UKB data field 22617_9111) 469 European ancestry cases, 113,372 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043561 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Fishing and agriculture related occupations n.e.c. (UKB data field 22617_9119) 222 European ancestry cases, 113,619 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043562 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Labourers in building and woodworking trades (UKB data field 22617_9121) 692 European ancestry cases, 113,149 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043563 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Labourers in other construction trades n.e.c. (UKB data field 22617_9129) 113 European ancestry cases, 113,728 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043564 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Industrial cleaning process occupations (UKB data field 22617_9132) 278 European ancestry cases, 113,563 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043565 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Printing machine minders and assistants (UKB data field 22617_9133) 155 European ancestry cases, 113,686 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043566 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Packers, bottlers, canners, fillers (UKB data field 22617_9134) 715 European ancestry cases, 113,126 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043567 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Labourers in process and plant operations n.e.c. (UKB data field 22617_9139) 1,247 European ancestry cases, 112,594 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043568 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Other goods handling and storage occupations n.e.c. (UKB data field 22617_9149) 1,649 European ancestry cases, 112,192 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043569 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Postal workers, mail sorters, messengers, couriers (UKB data field 22617_9211) 841 European ancestry cases, 113,000 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043570 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Elementary office occupations n.e.c. (UKB data field 22617_9219) 4,282 European ancestry cases, 109,559 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043571 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Hospital porters (UKB data field 22617_9221) 164 European ancestry cases, 113,677 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043572 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Hotel porters (UKB data field 22617_9222) 159 European ancestry cases, 113,682 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043573 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Kitchen and catering assistants (UKB data field 22617_9223) 660 European ancestry cases, 113,181 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043574 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Waiters, waitresses (UKB data field 22617_9224) 683 European ancestry cases, 113,158 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043575 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Bar staff (UKB data field 22617_9225) 804 European ancestry cases, 113,037 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043576 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Leisure and theme park attendants (UKB data field 22617_9226) 197 European ancestry cases, 113,644 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043577 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Elementary personal services occupations n.e.c. (UKB data field 22617_9229) 147 European ancestry cases, 113,694 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043578 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Cleaners, domestics (UKB data field 22617_9233) 868 European ancestry cases, 112,973 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043579 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Refuse and salvage occupations (UKB data field 22617_9235) 101 European ancestry cases, 113,740 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043580 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Security guards and related occupations (UKB data field 22617_9241) 368 European ancestry cases, 113,473 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043581 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: School mid-day assistants (UKB data field 22617_9244) 223 European ancestry cases, 113,618 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043582 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Elementary security occupations n.e.c. (UKB data field 22617_9249) 187 European ancestry cases, 113,654 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043583 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Shelf fillers (UKB data field 22617_9251) 539 European ancestry cases, 113,302 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043584 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job SOC coding: Elementary sales occupations n.e.c. (UKB data field 22617_9259) 276 European ancestry cases, 113,565 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90043585 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Hard margarine (UKB data field 20090_395) 200 European ancestry cases, 63,801 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042651 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Other type fat (UKB data field 20090_396) 507 European ancestry cases, 63,494 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042652 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of white wine glass drunk: small (125ml) (UKB data field 20095_1) 3,154 European ancestry cases, 60,847 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042653 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of white wine glass drunk: medium (175ml) (UKB data field 20095_2) 4,643 European ancestry cases, 59,358 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042654 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of white wine glass drunk: large (250ml) (UKB data field 20095_3) 615 European ancestry cases, 63,386 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042655 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of red wine glass drunk: small (125ml) (UKB data field 20096_1) 3,799 European ancestry cases, 60,202 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042656 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of red wine glass drunk: medium (175ml) (UKB data field 20096_2) 6,287 European ancestry cases, 57,714 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042657 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of red wine glass drunk: large (250ml) (UKB data field 20096_3) 937 European ancestry cases, 63,064 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042658 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of rose wine glass drunk: small (125ml) (UKB data field 20097_1) 669 European ancestry cases, 63,332 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042659 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of rose wine glass drunk: medium (175ml) (UKB data field 20097_2) 960 European ancestry cases, 63,041 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042660 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Size of rose wine glass drunk: large (250ml) (UKB data field 20097_3) 165 European ancestry cases, 63,836 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90042661 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Myeloproliferative disease (PheCode 200) 521 European ancestry cases, 455,827 European ancestry controls NA NR [11842647] (imputed) 0 myelodysplastic syndrome http://www.ebi.ac.uk/efo/EFO_0000198 GCST90042662 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Suffer from nerves (UKB data field 2010) 93,482 European ancestry cases, 346,059 European ancestry controls NA NR [11842647] (imputed) 0 feeling nervous measurement http://www.ebi.ac.uk/efo/EFO_0009597 GCST90042663 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Heart disease (UKB data field 20107_1) 131,326 European ancestry cases, 270,663 European ancestry controls NA NR [11842647] (imputed) 0 family history, heart disease http://www.ebi.ac.uk/efo/EFO_0000493, http://www.ebi.ac.uk/efo/EFO_0003777 GCST90042664 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Alzheimer's disease/dementia (UKB data field 20107_10) 19,003 European ancestry cases, 375,370 European ancestry controls NA NR [11842647] (imputed) 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90042665 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: PHESANT recoding (UKB data field 20107_100) 147,565 European ancestry cases, 249,556 European ancestry controls NA NR [11842647] (imputed) 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042666 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: PHESANT recoding (UKB data field 20107_101) 299,733 European ancestry cases, 102,148 European ancestry controls NA NR [11842647] (imputed) 1 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042667 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Parkinson's disease (UKB data field 20107_11) 9,960 European ancestry cases, 383,719 European ancestry controls NA NR [11842647] (imputed) 0 family history, Parkinson disease http://www.ebi.ac.uk/efo/EFO_0000493, http://purl.obolibrary.org/obo/MONDO_0005180 GCST90042668 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Severe depression (UKB data field 20107_12) 15,165 European ancestry cases, 378,924 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, family history http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042669 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Prostate cancer (UKB data field 20107_13) 30,487 European ancestry cases, 363,771 European ancestry controls NA NR [11842647] (imputed) 2 prostate cancer, family history http://purl.obolibrary.org/obo/MONDO_0008315, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042670 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Stroke (UKB data field 20107_2) 61,995 European ancestry cases, 335,148 European ancestry controls NA NR [11842647] (imputed) 0 stroke, family history http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042671 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Lung cancer (UKB data field 20107_3) 37,124 European ancestry cases, 359,064 European ancestry controls NA NR [11842647] (imputed) 1 family history of lung cancer http://www.ebi.ac.uk/efo/EFO_0006953 GCST90042672 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Bowel cancer (UKB data field 20107_4) 23,605 European ancestry cases, 370,895 European ancestry controls NA NR [11842647] (imputed) 0 intestinal cancer, family history http://www.ebi.ac.uk/efo/EFO_0007330, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042673 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: Chronic bronchitis/emphysema (UKB data field 20107_6) 45,946 European ancestry cases, 351,009 European ancestry controls NA NR [11842647] (imputed) 0 emphysema, family history, chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0000464, http://www.ebi.ac.uk/efo/EFO_0000493, http://www.ebi.ac.uk/efo/EFO_0006505 GCST90042674 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illnesses of father: High blood pressure (UKB data field 20107_8) 89,851 European ancestry cases, 307,528 European ancestry controls NA NR [11842647] (imputed) 0 hypertension, family history http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0000493 GCST90042675 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - paracetamol (UKB data field 20003_2038460150) 84,510 European ancestry cases, 371,766 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042576 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - Free-text entry, unable to be coded (UKB data field 20003_99999) 15,515 European ancestry cases, 440,761 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042577 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diet questionnaire performance: day-of-week questionnaire completion requested: Monday (UKB data field 20079_1) 10,057 European ancestry cases, 53,944 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042578 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diet questionnaire performance: day-of-week questionnaire completion requested: Tuesday (UKB data field 20079_2) 10,293 European ancestry cases, 53,708 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042579 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diet questionnaire performance: day-of-week questionnaire completion requested: Wednesday (UKB data field 20079_3) 10,684 European ancestry cases, 53,317 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042580 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diet questionnaire performance: day-of-week questionnaire completion requested: Thursday (UKB data field 20079_4) 10,756 European ancestry cases, 53,245 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042581 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diet questionnaire performance: day-of-week questionnaire completion requested: Friday (UKB data field 20079_5) 11,010 European ancestry cases, 52,991 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042582 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diet questionnaire performance: day-of-week questionnaire completion requested: Saturday (UKB data field 20079_6) 11,045 European ancestry cases, 52,956 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042583 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diet questionnaire performance: day-of-week questionnaire completion requested: Sunday (UKB data field 20079_7) 156 European ancestry cases, 63,845 European ancestry controls NA NR [11842647] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90042584 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Multivitamin (UKB data field 20084_468) 4,741 European ancestry cases, 59,260 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042585 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Multivitamin with iron (UKB data field 20084_469) 1,606 European ancestry cases, 62,395 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042586 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Multivitamin with calcium (UKB data field 20084_470) 379 European ancestry cases, 63,622 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042587 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Multivitamin with multimineral (UKB data field 20084_471) 3,731 European ancestry cases, 60,270 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042588 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Fish oil (UKB data field 20084_472) 15,374 European ancestry cases, 48,627 European ancestry controls NA NR [11842647] (imputed) 0 fish oil supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0600007 GCST90042589 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Glucosamine/chondroitin (UKB data field 20084_473) 9,683 European ancestry cases, 54,318 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042590 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Evening primrose (UKB data field 20084_474) 2,927 European ancestry cases, 61,074 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042591 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Vitamin A (UKB data field 20084_475) 631 European ancestry cases, 63,370 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042592 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Vitamin B6 (UKB data field 20084_476) 1,452 European ancestry cases, 62,549 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042593 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Vitamin B12 (UKB data field 20084_477) 1,305 European ancestry cases, 62,696 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042594 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Vitamin C (UKB data field 20084_478) 4,104 European ancestry cases, 59,897 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042595 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Vitamin D (UKB data field 20084_479) 2,049 European ancestry cases, 61,952 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042596 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Vitamin E (UKB data field 20084_480) 1,229 European ancestry cases, 62,772 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042597 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Folic acid (UKB data field 20084_481) 820 European ancestry cases, 63,181 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042598 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Chromium (UKB data field 20084_482) 264 European ancestry cases, 63,737 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042599 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Magnesium (UKB data field 20084_483) 1,018 European ancestry cases, 62,983 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042600 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Selenium (UKB data field 20084_484) 1,015 European ancestry cases, 62,986 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042601 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Calcium (UKB data field 20084_485) 3,617 European ancestry cases, 60,384 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042602 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Iron (UKB data field 20084_486) 894 European ancestry cases, 63,107 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042603 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Zinc (UKB data field 20084_487) 1,927 European ancestry cases, 62,074 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042604 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and/or mineral supplement use: Other vitamin (UKB data field 20084_488) 2,401 European ancestry cases, 61,600 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90042605 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of special diet followed: Low calorie (UKB data field 20086_10) 7,677 European ancestry cases, 56,324 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90042606 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of special diet followed: Vegetarian (UKB data field 20086_11) 2,156 European ancestry cases, 61,845 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90042607 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of special diet followed: Vegan (UKB data field 20086_12) 161 European ancestry cases, 63,840 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90042608 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of special diet followed: Other (UKB data field 20086_13) 2,168 European ancestry cases, 61,833 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90042609 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of special diet followed: Gluten-free (UKB data field 20086_8) 1,330 European ancestry cases, 62,671 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90042610 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of special diet followed: Lactose-free (UKB data field 20086_9) 890 European ancestry cases, 63,111 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90042611 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of meals eaten: Takeaway meals (UKB data field 20089_461) 2,574 European ancestry cases, 61,427 European ancestry controls NA NR [11842647] (imputed) 0 eating behaviour http://www.ebi.ac.uk/efo/EFO_0007829 GCST90042612 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of meals eaten: Restaurant meals (UKB data field 20089_462) 9,685 European ancestry cases, 54,316 European ancestry controls NA NR [11842647] (imputed) 0 eating behaviour http://www.ebi.ac.uk/efo/EFO_0007829 GCST90042613 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of meals eaten: Bought sandwiches (UKB data field 20089_463) 5,739 European ancestry cases, 58,262 European ancestry controls NA NR [11842647] (imputed) 0 eating behaviour http://www.ebi.ac.uk/efo/EFO_0007829 GCST90042614 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of meals eaten: Ready meals (UKB data field 20089_464) 5,003 European ancestry cases, 58,998 European ancestry controls NA NR [11842647] (imputed) 0 eating behaviour http://www.ebi.ac.uk/efo/EFO_0007829 GCST90042615 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of meals eaten: Home cooked meals (UKB data field 20089_465) 51,021 European ancestry cases, 12,980 European ancestry controls NA NR [11842647] (imputed) 0 eating behaviour http://www.ebi.ac.uk/efo/EFO_0007829 GCST90042616 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Cooking fat unknown (UKB data field 20090_352) 11,212 European ancestry cases, 52,789 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042617 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Olive oil (UKB data field 20090_353) 22,583 European ancestry cases, 41,418 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042618 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Sunflower oil (UKB data field 20090_354) 7,878 European ancestry cases, 56,123 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042619 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Vegetable oil (UKB data field 20090_355) 4,913 European ancestry cases, 59,088 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042620 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Rapeseed oil (UKB data field 20090_356) 1,452 European ancestry cases, 62,549 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042621 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Other oil (UKB data field 20090_357) 696 European ancestry cases, 63,305 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042622 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Butter (UKB data field 20090_359) 8,219 European ancestry cases, 55,782 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042623 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Spreadable butter (UKB data field 20090_360) 2,527 European ancestry cases, 61,474 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042624 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Low fat butter (UKB data field 20090_361) 665 European ancestry cases, 63,336 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042625 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - glucosamine product (UKB data field 20003_1141188442) 30,336 European ancestry cases, 425,940 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042526 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - humira 40mg injection solution 0.8ml prefilled syringe (UKB data field 20003_1141188594) 116 European ancestry cases, 456,160 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042527 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - asacol mr 400mg e/c tablet (UKB data field 20003_1141188658) 176 European ancestry cases, 456,100 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042528 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - felendil xl 5mg m/r tablet (UKB data field 20003_1141188836) 106 European ancestry cases, 456,170 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042529 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rosiglitazone 1mg / metformin 500mg tablet (UKB data field 20003_1141189090) 174 European ancestry cases, 456,102 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042530 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - avandamet 1mg / 500mg tablet (UKB data field 20003_1141189094) 169 European ancestry cases, 456,107 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042531 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cipralex 5mg tablet (UKB data field 20003_1141190158) 407 European ancestry cases, 455,869 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042532 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vascalpha 5mg m/r tablet (UKB data field 20003_1141190160) 142 European ancestry cases, 456,134 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042533 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tramacet 325mg/37.5mg tablet (UKB data field 20003_1141190960) 148 European ancestry cases, 456,128 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042534 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - levothyroxine sodium (UKB data field 20003_1141191044) 18,688 European ancestry cases, 437,588 European ancestry controls NA NR [11842647] (imputed) 5 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042535 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - respiratory mometasone (UKB data field 20003_1141191748) 258 European ancestry cases, 456,018 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042536 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dutasteride (UKB data field 20003_1141192000) 322 European ancestry cases, 208,446 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042537 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vardenafil (UKB data field 20003_1141192248) 119 European ancestry cases, 208,649 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042538 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rosuvastatin (UKB data field 20003_1141192410) 2,822 European ancestry cases, 453,454 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042539 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - crestor 10mg tablet (UKB data field 20003_1141192414) 289 European ancestry cases, 455,987 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042540 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ezetimibe (UKB data field 20003_1141192736) 2,667 European ancestry cases, 453,609 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042541 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ezetrol 10mg tablet (UKB data field 20003_1141192740) 851 European ancestry cases, 455,425 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042542 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - rino clenil 50micrograms nasal spray (UKB data field 20003_1141192916) 873 European ancestry cases, 455,403 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042543 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - testogel 50mg gel 5g sachet (UKB data field 20003_1141193272) 162 European ancestry cases, 456,114 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042544 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - olmesartan (UKB data field 20003_1141193282) 543 European ancestry cases, 455,733 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042545 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - olmetec 10mg tablet (UKB data field 20003_1141193346) 270 European ancestry cases, 456,006 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042546 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - allergy relief antihistamine 4mg tablet (UKB data field 20003_1141194224) 177 European ancestry cases, 456,099 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042547 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - telfast 30 tablet (UKB data field 20003_1141194386) 325 European ancestry cases, 455,951 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042548 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bendroflumethiazide (UKB data field 20003_1141194794) 25,484 European ancestry cases, 430,792 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042549 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bendroflumethiazide+potassium 2.5mg/7.7mmol m/r tablet (UKB data field 20003_1141194800) 102 European ancestry cases, 456,174 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042550 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Normal fat butter (UKB data field 20090_362) 4,644 European ancestry cases, 59,357 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042626 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Unknown fat butter (UKB data field 20090_363) 234 European ancestry cases, 63,767 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042627 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Lard (UKB data field 20090_364) 665 European ancestry cases, 63,336 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042628 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Olive spread (UKB data field 20090_365) 3,318 European ancestry cases, 60,683 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042629 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Very low fat olive spread (UKB data field 20090_366) 182 European ancestry cases, 63,819 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042630 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Low fat olive spread for (UKB data field 20090_367) 1,416 European ancestry cases, 62,585 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042631 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Normal fat olive spread (UKB data field 20090_368) 983 European ancestry cases, 63,018 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042632 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Cholesterol lowering olive spread (UKB data field 20090_369) 287 European ancestry cases, 63,714 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042633 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Unknown olive spread (UKB data field 20090_370) 206 European ancestry cases, 63,795 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042634 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Polyunsaturated margarine (UKB data field 20090_371) 5,221 European ancestry cases, 58,780 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042635 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Very low fat polyunsaturated margarine (UKB data field 20090_372) 372 European ancestry cases, 63,629 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042636 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Low fat polyunsaturated margarine (UKB data field 20090_373) 2,370 European ancestry cases, 61,631 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042637 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Normal fat polyunsaturated margarine (UKB data field 20090_374) 929 European ancestry cases, 63,072 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042638 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Cholesterol lowering polyunsaturated margarine (UKB data field 20090_375) 1,017 European ancestry cases, 62,984 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042639 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Unknown polyunsaturated margarine (UKB data field 20090_376) 174 European ancestry cases, 63,827 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042640 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Dairy spread (UKB data field 20090_377) 1,576 European ancestry cases, 62,425 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042641 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Low fat dairy spread (UKB data field 20090_379) 637 European ancestry cases, 63,364 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042642 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Normal fat dairy spread (UKB data field 20090_380) 640 European ancestry cases, 63,361 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042643 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Soya margarine (UKB data field 20090_383) 587 European ancestry cases, 63,414 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042644 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Low fat soya margarine (UKB data field 20090_385) 194 European ancestry cases, 63,807 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042645 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Normal fat soya margarine (UKB data field 20090_386) 179 European ancestry cases, 63,822 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042646 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Unknown/other soft margarine (UKB data field 20090_389) 958 European ancestry cases, 63,043 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042647 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Low fat soft margarine (UKB data field 20090_391) 255 European ancestry cases, 63,746 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042648 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Normal fat soft margarine (UKB data field 20090_392) 294 European ancestry cases, 63,707 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042649 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of fat/oil used in cooking: Unknown soft margarine (UKB data field 20090_394) 260 European ancestry cases, 63,741 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90042650 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hydroxycarbamide (UKB data field 20003_1141195044) 186 European ancestry cases, 456,090 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042551 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - formoterol (UKB data field 20003_1141195224) 118 European ancestry cases, 456,158 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042552 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - budesonide+formoterol (UKB data field 20003_1141195232) 308 European ancestry cases, 455,968 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042553 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cardioplen xl 5mg m/r tablet (UKB data field 20003_1141199858) 258 European ancestry cases, 456,018 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042554 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - pregabalin (UKB data field 20003_1141200004) 932 European ancestry cases, 455,344 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042555 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lyrica 25mg capsule (UKB data field 20003_1141200072) 126 European ancestry cases, 456,150 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042556 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cymalon cranberry 1.5g/5ml liquid (UKB data field 20003_1141200108) 163 European ancestry cases, 456,113 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042557 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - solifenacin (UKB data field 20003_1141200322) 701 European ancestry cases, 455,575 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042558 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vesicare 5mg tablet (UKB data field 20003_1141200384) 429 European ancestry cases, 455,847 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042559 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - duloxetine (UKB data field 20003_1141200564) 382 European ancestry cases, 455,894 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042560 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - strontium product (UKB data field 20003_1141200708) 138 European ancestry cases, 456,138 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042561 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - protelos 2g sachets (UKB data field 20003_1141200768) 112 European ancestry cases, 247,396 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042562 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - chondroitin product (UKB data field 20003_1187) 5,828 European ancestry cases, 450,448 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042563 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - co-enzyme q10/ubiquinone/bio-quinone/coenzyme q10 (UKB data field 20003_1189) 1,546 European ancestry cases, 454,730 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042564 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - omega-3/fish oil supplement (UKB data field 20003_1193) 17,179 European ancestry cases, 439,097 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042565 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin c product (UKB data field 20003_1195) 1,204 European ancestry cases, 455,072 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042566 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - evening primrose oil product (UKB data field 20003_1197) 1,018 European ancestry cases, 455,258 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042567 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - food supplement/plant/herbal extract (UKB data field 20003_1199) 1,697 European ancestry cases, 454,579 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042568 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - st john's wort/hypericum [ctsu] (UKB data field 20003_1201) 819 European ancestry cases, 455,457 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042569 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - aloe vera product (UKB data field 20003_1203) 452 European ancestry cases, 455,824 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042570 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - saw palmetto product (UKB data field 20003_1205) 512 European ancestry cases, 208,256 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042571 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - carbamazepine (UKB data field 20003_2038459704) 699 European ancestry cases, 455,577 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042572 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - digoxin (UKB data field 20003_2038459814) 1,172 European ancestry cases, 455,104 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042573 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - phenobarbitone (UKB data field 20003_2038460068) 122 European ancestry cases, 456,154 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042574 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - phenytoin (UKB data field 20003_2038460076) 416 European ancestry cases, 455,860 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042575 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - escitalopram (UKB data field 20003_1141180212) 811 European ancestry cases, 455,465 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042501 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amoxicillin (UKB data field 20003_1141180226) 359 European ancestry cases, 455,917 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042502 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ibandronic acid (UKB data field 20003_1141180314) 411 European ancestry cases, 455,865 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042503 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - beclometasone dipropionate+salbutamol (UKB data field 20003_1141180342) 279 European ancestry cases, 455,997 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042504 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cefalexin (UKB data field 20003_1141180392) 252 European ancestry cases, 456,024 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042505 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zirtek allergy 10mg tablet (UKB data field 20003_1141180662) 121 European ancestry cases, 456,155 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042506 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcium carbonate+colecalciferol 1.25g/5micrograms tablet (UKB data field 20003_1141180936) 200 European ancestry cases, 456,076 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042507 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - estriol product (UKB data field 20003_1141181594) 195 European ancestry cases, 247,313 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042508 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - estradiol product (UKB data field 20003_1141181700) 796 European ancestry cases, 246,712 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042509 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - omacor 1g capsule (UKB data field 20003_1141181868) 551 European ancestry cases, 455,725 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042510 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tiotropium (UKB data field 20003_1141182628) 1,143 European ancestry cases, 455,133 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042511 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - spiriva 18micrograms inhalation capsule (UKB data field 20003_1141182632) 655 European ancestry cases, 455,621 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042512 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cerazette 75micrograms tablet (UKB data field 20003_1141182800) 1,125 European ancestry cases, 246,383 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042513 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - xalacom 0.005%/0.5% eye drops (UKB data field 20003_1141184726) 245 European ancestry cases, 456,031 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042514 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - levocetirizine (UKB data field 20003_1141184748) 274 European ancestry cases, 456,002 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042515 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - travoprost (UKB data field 20003_1141185316) 161 European ancestry cases, 456,115 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042516 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - travatan 40micrograms/ml eye drops (UKB data field 20003_1141185326) 296 European ancestry cases, 455,980 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042517 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - care cetirizine hayfever relief 10mg tablet (UKB data field 20003_1141187230) 126 European ancestry cases, 456,150 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042518 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - codipar caplet (UKB data field 20003_1141187304) 102 European ancestry cases, 456,174 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042519 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nurofen 200mg tablet (UKB data field 20003_1141187776) 269 European ancestry cases, 456,007 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042520 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tadalafil (UKB data field 20003_1141187810) 557 European ancestry cases, 208,211 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042521 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cialis 10mg tablet (UKB data field 20003_1141187814) 250 European ancestry cases, 208,518 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042522 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cialis 20mg tablet (UKB data field 20003_1141187818) 163 European ancestry cases, 208,605 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042523 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - simvador 10mg tablet (UKB data field 20003_1141188146) 611 European ancestry cases, 455,665 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042524 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - berocca effervescent tablet (UKB data field 20003_1141188210) 104 European ancestry cases, 456,172 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042525 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for glasses/contact lenses: For 'astigmatism' (UKB data field 6147_4) 12,182 European ancestry cases, 443,472 European ancestry controls NA NR [11842647] (imputed) 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90044329 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for glasses/contact lenses: For a 'squint' or 'turn' in an eye since childhood (called 'strabismus') (UKB data field 6147_5) 1,936 European ancestry cases, 453,718 European ancestry controls NA NR [11842647] (imputed) 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90044330 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for glasses/contact lenses: For a 'lazy' eye or an eye with poor vision since childhood (called 'amblyopia') (UKB data field 6147_6) 3,694 European ancestry cases, 451,960 European ancestry controls NA NR [11842647] (imputed) 0 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST90044331 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for glasses/contact lenses: Other eye condition (UKB data field 6147_7) 1,572 European ancestry cases, 454,082 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90044332 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eye problems/disorders: Diabetes related eye disease (UKB data field 6148_1) 2,871 European ancestry cases, 145,108 European ancestry controls NA NR [11842647] (imputed) 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90044333 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eye problems/disorders: PHESANT recoding (UKB data field 6148_100) 115,304 European ancestry cases, 32,675 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90044334 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eye problems/disorders: Glaucoma (UKB data field 6148_2) 6,368 European ancestry cases, 141,611 European ancestry controls NA NR [11842647] (imputed) 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90044335 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eye problems/disorders: Injury or trauma resulting in loss of vision (UKB data field 6148_3) 2,717 European ancestry cases, 145,262 European ancestry controls NA NR [11842647] (imputed) 0 Visual loss http://purl.obolibrary.org/obo/HP_0000572 GCST90044336 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eye problems/disorders: Cataract (UKB data field 6148_4) 14,025 European ancestry cases, 133,954 European ancestry controls NA NR [11842647] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90044337 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eye problems/disorders: Macular degeneration (UKB data field 6148_5) 3,493 European ancestry cases, 144,486 European ancestry controls NA NR [11842647] (imputed) 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90044338 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Eye problems/disorders: Other serious eye condition (UKB data field 6148_6) 8,289 European ancestry cases, 139,690 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90044339 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mouth/teeth dental problems: Mouth ulcers (UKB data field 6149_1) 46,526 European ancestry cases, 408,039 European ancestry controls NA NR [11842647] (imputed) 0 Oral ulcer http://purl.obolibrary.org/obo/HP_0000155 GCST90044340 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mouth/teeth dental problems: PHESANT recoding (UKB data field 6149_100) 275,220 European ancestry cases, 179,345 European ancestry controls NA NR [11842647] (imputed) 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90044341 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mouth/teeth dental problems: Painful gums (UKB data field 6149_2) 13,055 European ancestry cases, 441,510 European ancestry controls NA NR [11842647] (imputed) 0 gingival disease, facial pain http://www.ebi.ac.uk/efo/EFO_0009670, http://www.ebi.ac.uk/efo/EFO_0009625 GCST90044342 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mouth/teeth dental problems: Bleeding gums (UKB data field 6149_3) 59,211 European ancestry cases, 395,354 European ancestry controls NA NR [11842647] (imputed) 0 Gingival bleeding http://purl.obolibrary.org/obo/HP_0000225 GCST90044343 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mouth/teeth dental problems: Loose teeth (UKB data field 6149_4) 18,545 European ancestry cases, 436,020 European ancestry controls NA NR [11842647] (imputed) 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90044344 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mouth/teeth dental problems: Toothache (UKB data field 6149_5) 18,555 European ancestry cases, 436,010 European ancestry controls NA NR [11842647] (imputed) 0 toothache http://www.ebi.ac.uk/efo/EFO_0010072 GCST90044345 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mouth/teeth dental problems: Dentures (UKB data field 6149_6) 77,191 European ancestry cases, 377,374 European ancestry controls NA NR [11842647] (imputed) 0 dentures http://www.ebi.ac.uk/efo/EFO_0010078 GCST90044346 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vascular/heart problems diagnosed by doctor: Heart attack (UKB data field 6150_1) 10,573 European ancestry cases, 444,730 European ancestry controls NA NR [11842647] (imputed) 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90044347 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vascular/heart problems diagnosed by doctor: PHESANT recoding (UKB data field 6150_100) 320,315 European ancestry cases, 134,988 European ancestry controls NA NR [11842647] (imputed) 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90044348 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vascular/heart problems diagnosed by doctor: Angina (UKB data field 6150_2) 14,618 European ancestry cases, 440,685 European ancestry controls NA NR [11842647] (imputed) 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90044349 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vascular/heart problems diagnosed by doctor: Stroke (UKB data field 6150_3) 6,986 European ancestry cases, 448,317 European ancestry controls NA NR [11842647] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90044350 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vascular/heart problems diagnosed by doctor: High blood pressure (UKB data field 6150_4) 122,620 European ancestry cases, 332,683 European ancestry controls NA NR [11842647] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90044351 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bone site(s): Ankle (UKB data field 6151_1) 6,388 European ancestry cases, 447,436 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044352 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bone site(s): Leg (UKB data field 6151_2) 2,950 European ancestry cases, 450,874 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044353 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bone site(s): Hip (UKB data field 6151_3) 813 European ancestry cases, 453,011 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044354 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bone site(s): Spine (UKB data field 6151_4) 1,023 European ancestry cases, 452,801 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044355 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bone site(s): Wrist (UKB data field 6151_5) 9,020 European ancestry cases, 444,804 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044356 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bone site(s): Arm (UKB data field 6151_6) 4,656 European ancestry cases, 449,168 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044357 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fractured bone site(s): Other bones (UKB data field 6151_7) 23,728 European ancestry cases, 430,096 European ancestry controls NA NR [11842647] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90044358 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Blood clot, DVT, bronchitis, emphysema, asthma, rhinitis, eczema, allergy diagnosed by doctor: PHESANT recoding (UKB data field 6152_100) 309,586 European ancestry cases, 145,863 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system disease, allergic disease, Abnormal thrombosis http://www.ebi.ac.uk/efo/EFO_0000684, http://purl.obolibrary.org/obo/MONDO_0005271, http://purl.obolibrary.org/obo/HP_0001977 GCST90044359 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Blood clot, DVT, bronchitis, emphysema, asthma, rhinitis, eczema, allergy diagnosed by doctor: Blood clot in the leg (DVT) (UKB data field 6152_5) 9,376 European ancestry cases, 446,073 European ancestry controls NA NR [11842647] (imputed) 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90044360 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Blood clot, DVT, bronchitis, emphysema, asthma, rhinitis, eczema, allergy diagnosed by doctor: Emphysema/chronic bronchitis (UKB data field 6152_6) 7,777 European ancestry cases, 447,672 European ancestry controls NA NR [11842647] (imputed) 0 emphysema, chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0000464, http://www.ebi.ac.uk/efo/EFO_0006505 GCST90044361 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Blood clot, DVT, bronchitis, emphysema, asthma, rhinitis, eczema, allergy diagnosed by doctor: Blood clot in the lung (UKB data field 6152_7) 3,796 European ancestry cases, 451,653 European ancestry controls NA NR [11842647] (imputed) 0 lung disease, Abnormal thrombosis http://www.ebi.ac.uk/efo/EFO_0003818, http://purl.obolibrary.org/obo/HP_0001977 GCST90044362 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Blood clot, DVT, bronchitis, emphysema, asthma, rhinitis, eczema, allergy diagnosed by doctor: Asthma (UKB data field 6152_8) 52,504 European ancestry cases, 402,945 European ancestry controls NA NR [11842647] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90044363 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Blood clot, DVT, bronchitis, emphysema, asthma, rhinitis, eczema, allergy diagnosed by doctor: Hayfever, allergic rhinitis or eczema (UKB data field 6152_9) 104,559 European ancestry cases, 350,890 European ancestry controls NA NR [11842647] (imputed) 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90044364 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure, diabetes, or take exogenous hormones: Cholesterol lowering medication (UKB data field 6153_1) 31,070 European ancestry cases, 215,100 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044365 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure, diabetes, or take exogenous hormones: PHESANT recoding (UKB data field 6153_100) 169,810 European ancestry cases, 76,360 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044366 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure, diabetes, or take exogenous hormones: Blood pressure medication (UKB data field 6153_2) 42,730 European ancestry cases, 203,440 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044367 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure, diabetes, or take exogenous hormones: Insulin (UKB data field 6153_3) 1,890 European ancestry cases, 244,280 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044368 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure, diabetes, or take exogenous hormones: Hormone replacement therapy (UKB data field 6153_4) 18,430 European ancestry cases, 227,740 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044369 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure, diabetes, or take exogenous hormones: Oral contraceptive pill or minipill (UKB data field 6153_5) 6,402 European ancestry cases, 239,768 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044370 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for pain relief, constipation, heartburn: Aspirin (UKB data field 6154_1) 63,593 European ancestry cases, 387,475 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044371 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for pain relief, constipation, heartburn: PHESANT recoding (UKB data field 6154_100) 249,433 European ancestry cases, 201,635 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044372 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for pain relief, constipation, heartburn: Ibuprofen (e.g. Nurofen) (UKB data field 6154_2) 67,072 European ancestry cases, 383,996 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044373 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for pain relief, constipation, heartburn: Paracetamol (UKB data field 6154_3) 99,397 European ancestry cases, 351,671 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044374 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for pain relief, constipation, heartburn: Ranitidine (e.g. Zantac) (UKB data field 6154_4) 8,741 European ancestry cases, 442,327 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044375 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for pain relief, constipation, heartburn: Omeprazole (e.g. Zanprol) (UKB data field 6154_5) 27,313 European ancestry cases, 423,755 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044376 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for pain relief, constipation, heartburn: Laxatives (e.g. Dulcolax, Senokot) (UKB data field 6154_6) 13,230 European ancestry cases, 437,838 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044377 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: Vitamin A (UKB data field 6155_1) 8,686 European ancestry cases, 445,105 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044378 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other abnormality of urination (PheCode 599.9) 1,049 European ancestry cases, 455,299 European ancestry controls NA NR [11842647] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90044254 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Electrocardiography test: phase duration (UKB data field 5992) 52,981 European ancestry cases, 14,144 European ancestry controls NA NR [11842647] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90044255 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other symptoms/disorders or the urinary system (PheCode 599) 3,841 European ancestry cases, 452,507 European ancestry controls NA NR [11842647] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90044256 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hyperplasia of prostate (PheCode 600) 6,505 European ancestry cases, 202,303 European ancestry controls NA NR [11842647] (imputed) 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90044257 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute prostatitis (PheCode 601.11) 163 European ancestry cases, 208,645 European ancestry controls NA NR [11842647] (imputed) 0 prostatitis http://www.ebi.ac.uk/efo/EFO_0003830 GCST90044258 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic prostatitis (PheCode 601.12) 500 European ancestry cases, 208,308 European ancestry controls NA NR [11842647] (imputed) 0 prostatitis http://www.ebi.ac.uk/efo/EFO_0003830 GCST90044259 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prostatitis (PheCode 601.1) 438 European ancestry cases, 208,370 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044260 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Balanoposthitis (PheCode 601.4) 205 European ancestry cases, 208,603 European ancestry controls NA NR [11842647] (imputed) 0 balanoposthitis http://purl.obolibrary.org/obo/MONDO_0001618 GCST90044261 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other inflammatory disorders of male genital organs (PheCode 601.8) 247 European ancestry cases, 208,561 European ancestry controls NA NR [11842647] (imputed) 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90044262 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chest pain felt during physical activity (UKB data field 6015) 2,453 European ancestry cases, 64,689 European ancestry controls NA NR [11842647] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90044263 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chest pain felt outside physical activity (UKB data field 6016) 2,103 European ancestry cases, 65,522 European ancestry controls NA NR [11842647] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90044264 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Able to walk or cycle unaided for 10 minutes (UKB data field 6017) 2,419 European ancestry cases, 64,405 European ancestry controls NA NR [11842647] (imputed) 0 ability to walk or cycle unaided for 10 minutes, self-reported http://www.ebi.ac.uk/efo/EFO_0009822 GCST90044265 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Electrocardiography test completion status: Fully completed (UKB data field 6020_1) 62,388 European ancestry cases, 4,748 European ancestry controls NA NR [11842647] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90044266 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Electrocardiography test completion status: Participant wanted to stop early (UKB data field 6020_31) 680 European ancestry cases, 66,456 European ancestry controls NA NR [11842647] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90044267 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Electrocardiography test completion status: Participant reported chest-pain and/or other discomfort (UKB data field 6020_32) 272 European ancestry cases, 66,864 European ancestry controls NA NR [11842647] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90044268 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Electrocardiography test completion status: Heart rate reached safety level (UKB data field 6020_33) 3,616 European ancestry cases, 63,520 European ancestry controls NA NR [11842647] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90044269 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Electrocardiography test completion status: Incomplete - other reason (UKB data field 6020_34) 180 European ancestry cases, 66,956 European ancestry controls NA NR [11842647] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90044270 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of prostate (PheCode 602) 805 European ancestry cases, 208,003 European ancestry controls NA NR [11842647] (imputed) 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90044271 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hydrocele (PheCode 603.1) 1,165 European ancestry cases, 207,643 European ancestry controls NA NR [11842647] (imputed) 0 testicular hydrocele http://www.ebi.ac.uk/efo/EFO_1001859 GCST90044272 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of the kidney and ureters (PheCode 586) 445 European ancestry cases, 455,903 European ancestry controls NA NR [11842647] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90044229 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pyelonephritis (PheCode 590) 1,169 European ancestry cases, 455,179 European ancestry controls NA NR [11842647] (imputed) 0 nephritis http://www.ebi.ac.uk/efo/EFO_1002050 GCST90044230 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Urinary tract infection (PheCode 591) 7,703 European ancestry cases, 448,645 European ancestry controls NA NR [11842647] (imputed) 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90044231 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Acute cystitis (PheCode 592.11) 120 European ancestry cases, 456,228 European ancestry controls NA NR [11842647] (imputed) 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90044232 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic cystitis (PheCode 592.12) 599 European ancestry cases, 455,749 European ancestry controls NA NR [11842647] (imputed) 0 chronic cystitis http://www.ebi.ac.uk/efo/EFO_1000023 GCST90044233 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic interstitial cystitis (PheCode 592.13) 240 European ancestry cases, 456,108 European ancestry controls NA NR [11842647] (imputed) 0 chronic interstitial cystitis http://www.ebi.ac.uk/efo/EFO_1000869 GCST90044234 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cystitis (PheCode 592.1) 1,324 European ancestry cases, 455,024 European ancestry controls NA NR [11842647] (imputed) 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90044235 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hematuria (PheCode 593) 15,001 European ancestry cases, 441,347 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044236 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Calculus of kidney (PheCode 594.1) 2,766 European ancestry cases, 453,582 European ancestry controls NA NR [11842647] (imputed) 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90044237 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Calculus of lower urinary tract (PheCode 594.2) 614 European ancestry cases, 455,734 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044238 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Calculus of ureter (PheCode 594.3) 2,456 European ancestry cases, 453,892 European ancestry controls NA NR [11842647] (imputed) 0 ureterolithiasis http://www.ebi.ac.uk/efo/EFO_1001228 GCST90044239 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Renal colic (PheCode 594.8) 1,833 European ancestry cases, 454,515 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044240 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Urinary calculus (PheCode 594) 438 European ancestry cases, 455,910 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044241 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hydronephrosis (PheCode 595) 1,230 European ancestry cases, 455,118 European ancestry controls NA NR [11842647] (imputed) 0 hydronephrosis http://www.ebi.ac.uk/efo/EFO_0005562 GCST90044242 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bladder neck obstruction (PheCode 596.1) 1,621 European ancestry cases, 454,727 European ancestry controls NA NR [11842647] (imputed) 0 bladder neck obstruction http://www.ebi.ac.uk/efo/EFO_1000840 GCST90044243 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Functional disorders of bladder (PheCode 596.5) 1,362 European ancestry cases, 454,986 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044244 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of bladder (PheCode 596) 4,182 European ancestry cases, 452,166 European ancestry controls NA NR [11842647] (imputed) 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90044245 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Urethral stricture (not specified as infectious) (PheCode 597.1) 2,700 European ancestry cases, 453,648 European ancestry controls NA NR [11842647] (imputed) 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90044246 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of urethra and urinary tract (PheCode 597) 495 European ancestry cases, 455,853 European ancestry controls NA NR [11842647] (imputed) 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90044247 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal findings on examination of urine (PheCode 598) 2,540 European ancestry cases, 453,808 European ancestry controls NA NR [11842647] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90044248 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Urinary obstruction (PheCode 599.1) 105 European ancestry cases, 456,243 European ancestry controls NA NR [11842647] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90044249 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Retention of urine (PheCode 599.2) 3,060 European ancestry cases, 453,288 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044250 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dysuria (PheCode 599.3) 473 European ancestry cases, 455,875 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044251 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Urinary incontinence (PheCode 599.4) 6,669 European ancestry cases, 449,679 European ancestry controls NA NR [11842647] (imputed) 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90044252 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Frequency of urination and polyuria (PheCode 599.5) 2,295 European ancestry cases, 454,053 European ancestry controls NA NR [11842647] (imputed) 0 Polyuria http://purl.obolibrary.org/obo/HP_0000103 GCST90044253 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal spermatozoa (PheCode 609.2) 134 European ancestry cases, 208,674 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal male internal genitalia morphology http://purl.obolibrary.org/obo/HP_0000022 GCST90044279 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cystic mastopathy (PheCode 610.1) 622 European ancestry cases, 246,918 European ancestry controls NA NR [11842647] (imputed) 0 breast benign neoplasm http://purl.obolibrary.org/obo/MONDO_0000620 GCST90044280 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fibroadenosis of breast (PheCode 610.2) 147 European ancestry cases, 247,393 European ancestry controls NA NR [11842647] (imputed) 0 breast adenosis http://www.ebi.ac.uk/efo/EFO_0006891 GCST90044281 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fibrosclerosis of breast (PheCode 610.3) 183 European ancestry cases, 247,357 European ancestry controls NA NR [11842647] (imputed) 0 breast disease http://www.ebi.ac.uk/efo/EFO_0009483 GCST90044282 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of breast (PheCode 610.4) 1,425 European ancestry cases, 454,923 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90044283 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other specified benign mammary dysplasias (PheCode 610.8) 551 European ancestry cases, 455,797 European ancestry controls NA NR [11842647] (imputed) 0 breast benign neoplasm http://purl.obolibrary.org/obo/MONDO_0000620 GCST90044284 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Lump or mass in breast (PheCode 611.3) 1,545 European ancestry cases, 454,803 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044285 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypertrophy of breast (Gynecomastia) (PheCode 612.2) 739 European ancestry cases, 455,609 European ancestry controls NA NR [11842647] (imputed) 0 Breast hypertrophy http://purl.obolibrary.org/obo/HP_0010313 GCST90044286 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Inflammatory disease of breast (PheCode 613.1) 592 European ancestry cases, 455,756 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044287 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other signs and symptoms in breast (PheCode 613.7) 450 European ancestry cases, 455,898 European ancestry controls NA NR [11842647] (imputed) 0 breast disease http://www.ebi.ac.uk/efo/EFO_0009483 GCST90044288 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other specified disorders of breast (PheCode 613.8) 265 European ancestry cases, 247,275 European ancestry controls NA NR [11842647] (imputed) 0 breast disease http://www.ebi.ac.uk/efo/EFO_0009483 GCST90044289 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breast disorder, not otherwise specified (PheCode 613.9) 178 European ancestry cases, 247,362 European ancestry controls NA NR [11842647] (imputed) 0 breast disease http://www.ebi.ac.uk/efo/EFO_0009483 GCST90044290 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Qualifications: College or University degree (UKB data field 6138_1) 145,251 European ancestry cases, 306,346 European ancestry controls NA NR [11842647] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90044291 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Qualifications: PHESANT recoding (UKB data field 6138_100) 78,851 European ancestry cases, 372,746 European ancestry controls NA NR [11842647] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90044292 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Qualifications: A levels/AS levels or equivalent (UKB data field 6138_2) 121,822 European ancestry cases, 329,775 European ancestry controls NA NR [11842647] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90044293 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Qualifications: O levels/GCSEs or equivalent (UKB data field 6138_3) 210,244 European ancestry cases, 241,353 European ancestry controls NA NR [11842647] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90044294 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Qualifications: CSEs or equivalent (UKB data field 6138_4) 59,415 European ancestry cases, 392,182 European ancestry controls NA NR [11842647] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90044295 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Qualifications: NVQ or HND or HNC or equivalent (UKB data field 6138_5) 84,091 European ancestry cases, 367,506 European ancestry controls NA NR [11842647] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90044296 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Qualifications: Other professional qualifications eg: nursing, teaching (UKB data field 6138_6) 129,492 European ancestry cases, 322,105 European ancestry controls NA NR [11842647] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90044297 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pelvic peritoneal adhesions, female (postoperative) (postinfection) (PheCode 614.1) 575 European ancestry cases, 246,965 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90044298 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic inflammatory pelvic disease (PheCode 614.32) 188 European ancestry cases, 247,352 European ancestry controls NA NR [11842647] (imputed) 0 Pelvic Inflammatory Disease http://www.ebi.ac.uk/efo/EFO_1001388 GCST90044299 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pelvic inflammatory disease, not otherwise specified (PheCode 614.33) 224 European ancestry cases, 247,316 European ancestry controls NA NR [11842647] (imputed) 0 Pelvic Inflammatory Disease http://www.ebi.ac.uk/efo/EFO_1001388 GCST90044300 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Inflammatory diseases of uterus, except cervix (PheCode 614.4) 159 European ancestry cases, 247,381 European ancestry controls NA NR [11842647] (imputed) 0 uterine inflammatory disease http://www.ebi.ac.uk/efo/EFO_0009572 GCST90044301 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cervicitis and endocervicitis (PheCode 614.51) 451 European ancestry cases, 247,089 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044302 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vaginitis and vulvovaginitis (PheCode 614.52) 261 European ancestry cases, 247,279 European ancestry controls NA NR [11842647] (imputed) 0 vulvovaginitis http://www.ebi.ac.uk/efo/EFO_1001240 GCST90044303 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cyst or abscess of Bartholin's gland (PheCode 614.53) 756 European ancestry cases, 246,784 European ancestry controls NA NR [11842647] (imputed) 0 Bartholin gland disease http://www.ebi.ac.uk/efo/EFO_0009469 GCST90044304 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abscess or ulceration of vulva (PheCode 614.54) 244 European ancestry cases, 247,296 European ancestry controls NA NR [11842647] (imputed) 0 ulceration of vulva http://purl.obolibrary.org/obo/MONDO_0001551 GCST90044305 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Inflammatory disease of cervix, vagina, and vulva (PheCode 614.5) 116 European ancestry cases, 247,424 European ancestry controls NA NR [11842647] (imputed) 0 uterine inflammatory disease http://www.ebi.ac.uk/efo/EFO_0009572 GCST90044306 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. How are people in household related to participant: Husband, wife or partner (UKB data field 6141_1) 333,559 European ancestry cases, 119,887 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90044307 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. How are people in household related to participant: Son and/or daughter (include step-children) (UKB data field 6141_2) 153,215 European ancestry cases, 300,231 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90044308 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. How are people in household related to participant: Mother and/or father (UKB data field 6141_4) 8,242 European ancestry cases, 445,204 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90044309 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. How are people in household related to participant: Grandparent (UKB data field 6141_5) 124 European ancestry cases, 453,322 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90044310 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. How are people in household related to participant: Grandchild (UKB data field 6141_6) 3,724 European ancestry cases, 449,722 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90044311 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. How are people in household related to participant: Other related (UKB data field 6141_7) 2,595 European ancestry cases, 450,851 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90044312 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. How are people in household related to participant: Other unrelated (UKB data field 6141_8) 8,054 European ancestry cases, 445,392 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90044313 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Never eat eggs, dairy, wheat, sugar: Eggs or foods containing eggs (UKB data field 6144_1) 11,911 European ancestry cases, 442,588 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90044314 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Never eat eggs, dairy, wheat, sugar: Dairy products (UKB data field 6144_2) 10,179 European ancestry cases, 444,320 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90044315 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Never eat eggs, dairy, wheat, sugar: Wheat products (UKB data field 6144_3) 12,203 European ancestry cases, 442,296 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90044316 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Never eat eggs, dairy, wheat, sugar: Sugar or foods/drinks containing sugar (UKB data field 6144_4) 85,521 European ancestry cases, 368,978 European ancestry controls NA NR [11842647] (imputed) 0 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST90044317 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Never eat eggs, dairy, wheat, sugar: I eat all of the above (UKB data field 6144_5) 350,709 European ancestry cases, 103,790 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90044318 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illness, injury, bereavement, stress in last 2 years: Serious illness, injury or assault to yourself (UKB data field 6145_1) 42,167 European ancestry cases, 411,079 European ancestry controls NA NR [11842647] (imputed) 0 injury, trauma exposure measurement, disease http://www.ebi.ac.uk/efo/EFO_0000546, http://www.ebi.ac.uk/efo/EFO_0010703, http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044319 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illness, injury, bereavement, stress in last 2 years: PHESANT recoding (UKB data field 6145_100) 253,501 European ancestry cases, 199,745 European ancestry controls NA NR [11842647] (imputed) 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90044320 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illness, injury, bereavement, stress in last 2 years: Serious illness, injury or assault of a close relative (UKB data field 6145_2) 52,628 European ancestry cases, 400,618 European ancestry controls NA NR [11842647] (imputed) 0 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST90044321 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illness, injury, bereavement, stress in last 2 years: Death of a close relative (UKB data field 6145_3) 95,788 European ancestry cases, 357,458 European ancestry controls NA NR [11842647] (imputed) 0 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST90044322 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illness, injury, bereavement, stress in last 2 years: Death of a spouse or partner (UKB data field 6145_4) 7,176 European ancestry cases, 446,070 European ancestry controls NA NR [11842647] (imputed) 0 trauma exposure measurement http://www.ebi.ac.uk/efo/EFO_0010703 GCST90044323 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illness, injury, bereavement, stress in last 2 years: Marital separation/divorce (UKB data field 6145_5) 13,871 European ancestry cases, 439,375 European ancestry controls NA NR [11842647] (imputed) 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90044324 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Illness, injury, bereavement, stress in last 2 years: Financial difficulties (UKB data field 6145_6) 52,374 European ancestry cases, 400,872 European ancestry controls NA NR [11842647] (imputed) 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90044325 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for glasses/contact lenses: For short-sightedness (called 'myopia') (UKB data field 6147_1) 36,623 European ancestry cases, 419,031 European ancestry controls NA NR [11842647] (imputed) 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90044326 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for glasses/contact lenses: For long-sightedness, i.e. for distance and near, but particularly for near tasks like reading (called 'hypermetropia') (UKB data field 6147_2) 18,730 European ancestry cases, 436,924 European ancestry controls NA NR [11842647] (imputed) 0 Hypermetropia http://purl.obolibrary.org/obo/HP_0000540 GCST90044327 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for glasses/contact lenses: For just reading/near work as you are getting older (called 'presbyopia') (UKB data field 6147_3) 39,080 European ancestry cases, 416,574 European ancestry controls NA NR [11842647] (imputed) 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90044328 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Target heart rate achieved (UKB data field 6034) 6,842 European ancestry cases, 60,283 European ancestry controls NA NR [11842647] (imputed) 0 achievement of target heart rate, self-reported http://www.ebi.ac.uk/efo/EFO_0009823 GCST90044273 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of testis (PheCode 603) 847 European ancestry cases, 207,961 European ancestry controls NA NR [11842647] (imputed) 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90044274 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Redundant prepuce and phimosis/BXO (PheCode 604.1) 2,630 European ancestry cases, 206,178 European ancestry controls NA NR [11842647] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90044275 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of penis (PheCode 604) 523 European ancestry cases, 208,285 European ancestry controls NA NR [11842647] (imputed) 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90044276 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Erectile dysfunction [ED] (PheCode 605) 357 European ancestry cases, 208,451 European ancestry controls NA NR [11842647] (imputed) 0 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST90044277 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other disorders of male genital organs (PheCode 608) 2,255 European ancestry cases, 206,553 European ancestry controls NA NR [11842647] (imputed) 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90044278 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Urinary potassium excretion 332,398 European ancestry individuals, 5,786 African ancestry individuals, 6,998 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 1 potassium measurement http://www.ebi.ac.uk/efo/EFO_0009283 GCST90019517 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Sex hormone-binding globulin levels 310,323 European ancestry individuals, 5,523 African ancestry individuals, 6,638 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 415 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90019518 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Urinary sodium excretion 332,397 European ancestry individuals, 5,781 African ancestry individuals, 6,993 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 15 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST90019519 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Testosterone levels 310,461 European ancestry individuals, 5,453 African ancestry individuals, 6,680 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 113 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90019520 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Total bilirubin levels 341,077 European ancestry individuals, 5,978 African ancestry individuals, 7,313 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 260 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90019521 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Serum total protein levels 313,032 European ancestry individuals, 5,573 African ancestry individuals, 6,687 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 239 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019522 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Triglyceride levels 342,233 European ancestry individuals, 6,014 African ancestry individuals, 7,330 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 424 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90019523 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Urate levels 342,087 European ancestry individuals, 6,011 African ancestry individuals, 7,328 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 363 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90019524 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Urea levels 342,286 European ancestry individuals, 6,015 African ancestry individuals, 7,336 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 166 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90019525 Genome-wide genotyping array 2021-06-29 33462484 Sinnott-Armstrong N 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462484 Genetics of 35 blood and urine biomarkers in the UK Biobank. Vitamin D levels 327,435 European ancestry individuals, 5,845 African ancestry individuals, 6,425 South Asian ancestry individuals NA Affymetrix [9000000] (imputed) 142 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90019526 Genome-wide genotyping array 2022-09-07 35898629 Yin B 2022-07-11 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35898629 Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis. Decaffeinated coffee consumption and/or alcohol use disorder score 64,717 decaffeinated coffee drinking cases, 121,604 individuals with alcohol use measurements, 264,954 controls NA NR [NR] 1 coffee consumption measurement, alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0006781, http://www.ebi.ac.uk/efo/EFO_0009458 GCST90134525 Genome-wide genotyping array 2022-09-07 35898629 Yin B 2022-07-11 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35898629 Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis. Decaffeinated coffee consumption and/or alcohol consumption score 64,717 decaffeinated coffee drinking cases, 121,604 individuals with alcohol use measurements, 264,954 controls NA NR [NR] 1 coffee consumption measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781, http://www.ebi.ac.uk/efo/EFO_0007878 GCST90134526 Genome-wide genotyping array 2022-09-07 35898629 Yin B 2022-07-11 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35898629 Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis. Decaffeinated coffee consumption and/or alcohol dependence and hazardous-use score 64,717 decaffeinated coffee drinking cases, 121,604 individuals with alcohol use measurements, 264,954 controls NA NR [NR] 2 coffee consumption measurement, alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0006781, http://www.ebi.ac.uk/efo/EFO_0007835 GCST90134527 Genome-wide genotyping array 2022-09-07 35898629 Yin B 2022-07-11 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35898629 Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis. Decaffeinated coffee consumption and/or lifetime cannabis use 64,717 decaffeinated coffee drinking cases, 43,380 lifetime cannabis use cases, 383,656 controls NA NR [NR] 5 coffee consumption measurement, Cannabis use http://www.ebi.ac.uk/efo/EFO_0006781, http://www.ebi.ac.uk/efo/EFO_0007585 GCST90134528 Genome-wide genotyping array 2022-09-07 35898629 Yin B 2022-07-11 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35898629 Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis. Decaffeinated coffee consumption or major depression disorder 64,717 decaffeinated coffee drinking cases, 170,756 major depressive disorder cases, 594,397 controls NA NR [NR] 27 coffee consumption measurement, major depressive disorder http://www.ebi.ac.uk/efo/EFO_0006781, http://purl.obolibrary.org/obo/MONDO_0002009 GCST90134529 Genome-wide genotyping array 2022-09-07 35898629 Yin B 2022-07-11 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35898629 Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis. Decaffeinated coffee consumption and/or neuroticism 64,717 decaffeinated coffee drinking cases, 380,060 individuals with neuroticism measurements, 264,954 controls NA NR [NR] 31 coffee consumption measurement, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0006781, http://www.ebi.ac.uk/efo/EFO_0007660 GCST90134530 Genome-wide genotyping array 2022-09-07 35898629 Yin B 2022-07-11 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/35898629 Shared Genetics and Causality Between Decaffeinated Coffee Consumption and Neuropsychiatric Diseases: A Large-Scale Genome-Wide Cross-Trait Analysis and Mendelian Randomization Analysis. Decaffeinated coffee consumption and/or insomnia 64,717 decaffeinated coffee drinking cases, 386,533 individuals with insomnia measurements, 264,954 controls NA NR [NR] 6 coffee consumption measurement, insomnia http://www.ebi.ac.uk/efo/EFO_0006781, http://www.ebi.ac.uk/efo/EFO_0004698 GCST90134531 Genome-wide genotyping array 2022-06-01 35238325 Lee YH 2022-02-21 Genet Mol Biol www.ncbi.nlm.nih.gov/pubmed/35238325 APOE and KLF14 genetic variants are sex-specific for low high-density lipoprotein cholesterol identified by a genome-wide association study. Low high density lipoprotein cholesterol levels 20,763 Taiwanese ancestry males NA Affymetrix [NR] 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90103982 Genome-wide genotyping array 2022-06-01 35238325 Lee YH 2022-02-21 Genet Mol Biol www.ncbi.nlm.nih.gov/pubmed/35238325 APOE and KLF14 genetic variants are sex-specific for low high-density lipoprotein cholesterol identified by a genome-wide association study. Low high density lipoprotein cholesterol levels 20,763 Taiwanese ancestry females NA Affymetrix [NR] 8 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90103983 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Depression severity x hours spent using computers interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 8 lifestyle measurement, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007006 GCST90101754 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Cigarette consumption x hours spent using computers interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 61 lifestyle measurement, maximum cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0009264 GCST90101755 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Alcohol consumption x hours spent using computers interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 21 lifestyle measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007878 GCST90101756 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Anxiety severity x playing computer games interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 58 lifestyle measurement, anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007795 GCST90101757 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Depression severity x playing computer games interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 25 lifestyle measurement, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007006 GCST90101758 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Cigarette consumption x playing computer games interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 17 lifestyle measurement, maximum cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0009264 GCST90101759 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Alcohol consumption x playing computer games interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 27 lifestyle measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007878 GCST90101760 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Anxiety severity x hours spent watching television interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 42 lifestyle measurement, anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007795 GCST90101749 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Depression severity x hours spent watching television interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 46 lifestyle measurement, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007006 GCST90101750 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Cigarette consumption x hours spent watching television interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 8 lifestyle measurement, maximum cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0009264 GCST90101751 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Alcohol consumption x hours spent watching television interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 42 lifestyle measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007878 GCST90101752 Genome-wide genotyping array 2022-04-08 34877740 Ye J 2021-12-07 Addict Biol www.ncbi.nlm.nih.gov/pubmed/34877740 Associations between electronic devices use and common mental traits: A gene-environment interaction model using the UK Biobank data. Anxiety severity x hours spent using computers interaction 488,377 British ancestry individuals NA Affymetrix [NR] (imputed) 9 lifestyle measurement, anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0010724, http://www.ebi.ac.uk/efo/EFO_0007795 GCST90101753 Genome-wide genotyping array 2022-04-04 34926279 Lu Y 2021-12-03 Front Oncol www.ncbi.nlm.nih.gov/pubmed/34926279 Identification of Recessively Inherited Genetic Variants Potentially Linked to Pancreatic Cancer Risk. Pancreatic cancer 8,769 European ancestry cases, 7,055 European ancestry controls 70 Brazilian ancestry cases, 250 Brazilian ancestry controls, 3,212 European or unknown ancestry cases, 3,470 European or unknown ancestry controls Illumina [5056279] (imputed) 3 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90100588 Genome-wide genotyping array 2022-05-26 35167971 Leffers HCB 2022-02-12 Joint Bone Spine www.ncbi.nlm.nih.gov/pubmed/35167971 Established risk loci for systemic lupus erythematosus at NCF2, STAT4, TNPO3, IRF5 and ITGAM associate with distinct clinical manifestations: a Danish genome-wide association study. Systemic lupus erythematosus 427 European ancestry cases, 89,699 European ancestry controls NA Illumina [654027] 5 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90103801 Genome-wide genotyping array 2022-06-20 35312098 Ngwa JS 2022-03-21 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35312098 Secondary analyses for genome-wide association studies using expression quantitative trait loci. Platelet aggregation 806 European ancestry individuals from 196 families NA NR [9769070] 1 platelet aggregation http://purl.obolibrary.org/obo/GO_0070527 GCST90104704 Genome-wide sequencing 2022-06-20 35312098 Ngwa JS 2022-03-21 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35312098 Secondary analyses for genome-wide association studies using expression quantitative trait loci. Platelet aggregation 661 African American individuals from 190 families NA NR [16415214] 2 platelet aggregation http://purl.obolibrary.org/obo/GO_0070527 GCST90104705 Genome-wide sequencing 2022-06-20 35312098 Ngwa JS 2022-03-21 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/35312098 Secondary analyses for genome-wide association studies using expression quantitative trait loci. Platelet aggregation 806 European ancestry individuals from 196 families, 661 African American individuals from 190 families NA NR [8242287] 2 platelet aggregation http://purl.obolibrary.org/obo/GO_0070527 GCST90104706 Genome-wide sequencing 2022-04-04 34878701 Fan L 2021-12-08 Oral Dis www.ncbi.nlm.nih.gov/pubmed/34878701 A Genome-wide Association Study of Premolar Agenesis in a Chinese Population. Tooth agenesis (mandibular second premolars) 191 Han Chinese ancestry cases, 1,195 Han Chinese ancestry controls NA Illumina [5585618] (imputed) 4 tooth agenesis http://www.ebi.ac.uk/efo/EFO_0005410 GCST90100589 Genome-wide genotyping array 2022-07-01 35352885 Lee CJ 2022-04-01 Yonsei Med J www.ncbi.nlm.nih.gov/pubmed/35352885 Genetic Variants Associated with Adverse Events after Angiotensin-Converting Enzyme Inhibitor Use: Replication after GWAS-Based Discovery. Adverse response to angiotensin-converting enzyme inhibitor 143 Korean ancestry cases, 85 Korean ancestry controls 212 Korean ancestry cases, 124 Korean ancestry controls NR [668091] 0 response to angiotensin-converting enzyme inhibitor http://www.ebi.ac.uk/efo/EFO_0005325 GCST90105048 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-24809 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104964 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Ethylmalonate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104965 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-12112 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104966 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-24983 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104967 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Butyrylcarnitine (C4) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104968 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetylarginine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104969 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetylasparagine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104970 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetylcitrulline levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104971 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 3-aminoisobutyrate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90104972 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N2-acetyllysine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104973 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetylkynurenine (2) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104974 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Glycochenodeoxycholate glucuronide (1) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104975 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 2'-o-methyluridine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90104976 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-12798 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104977 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Bilirubin (z,z) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90104978 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-delta-acetylornithine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104979 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-11491 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104980 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Biliverdin levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90104981 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Fibrinopeptide A (3-15) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104982 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 5-acetylamino-6-formylamino-3-methyluracil levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104983 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Bilirubin (E,E) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90104984 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Bilirubin (E,Z or Z,E) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90104985 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetylputrescine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104986 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 2'-o-methylcytidine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90104987 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104988 Genome-wide genotyping array 2021-11-22 34741163 Eijsbouts C 2021-11-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34741163 Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders. Irritable bowel syndrome 53,400 European ancestry cases, 433,201 European ancestry controls 205,252 European ancestry cases, 1,384,055 European ancestry controls Illumina [9885498] (imputed) 6 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90016564 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-21792 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104989 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104990 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 3-methylcytidine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90104991 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-11530 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104992 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 1-arachidonoyl-gpc (20:4n6) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104993 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-24849 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104994 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-11522 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104995 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-21448 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104996 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-12117 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104997 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Hexadecanedioate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104998 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetylphenylalanine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90104999 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetyl-aspartyl-glutamate (naag) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105000 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-11593 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105001 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Glycine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90105002 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Glycodeoxycholate glucuronide (1) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105003 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-16946 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105004 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetyl-1-methylhistidine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105005 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetyltyrosine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105006 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-19141 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105007 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Methionine sulfone levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105008 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Methyl glucopyranoside (alpha + beta) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105009 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105010 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 2-aminooctanoate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105011 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Dimethylglycine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90105012 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-24747 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105013 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-13431 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105014 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-methylpipecolate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105015 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Pregnenetriol disulfate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105016 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105017 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Gamma-glutamylglycine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105018 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-21441 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105019 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 5alpha-pregnan-3beta,20alpha-diol monosulfate (1) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105020 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. N-acetylglutamine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105021 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Imidazole lactate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105022 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-18921 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105023 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Fexofenadine levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105024 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Glycocholenate sulfate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105025 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Hexadecenedioate (C16:1-DC) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105026 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Taurochenodeoxycholic acid 3-sulfate levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105027 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Valsartan levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105028 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. Naringenin levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105029 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. X-23314 levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90105030 Genome-wide genotyping array 2022-07-01 33177712 Bar N 2020-11-11 Nature www.ncbi.nlm.nih.gov/pubmed/33177712 A reference map of potential determinants for the human serum metabolome. 5-methyluridine (ribothymidine) levels 1,170 Israeli ancestry individuals NA Illumina [NR] (imputed) 1 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90105031 Genome-wide genotyping array 2022-04-22 35393395 Okhuijsen-Pfeifer C 2022-04-07 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35393395 Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders. Symptom severity in clozapine treated schizophrenia spectrum disorders (quantitative) 684 individuals NA Illumina [5506411] (imputed) 1 schizophrenia symptom severity measurement, response to clozapine http://www.ebi.ac.uk/efo/EFO_0007927, http://purl.obolibrary.org/obo/GO_0097338 GCST90101840 Genome-wide genotyping array 2022-04-22 35393395 Okhuijsen-Pfeifer C 2022-04-07 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35393395 Genome-wide association analyses of symptom severity among clozapine-treated patients with schizophrenia spectrum disorders. Symptom severity in clozapine treated schizophrenia spectrum disorders (binary) 354 cases, 330 controls NA Illumina [5506411] (imputed) 1 schizophrenia symptom severity measurement, response to clozapine http://www.ebi.ac.uk/efo/EFO_0007927, http://purl.obolibrary.org/obo/GO_0097338 GCST90101841 Genome-wide genotyping array 2022-07-21 35383711 Thomeas-McEwing V 2022-04-07 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/35383711 Two polymorphic gene loci associated with treprostinil dose in pulmonary arterial hypertension. Treprostinil dose in pulmonary arterial hypertension 98 European ancestry individuals NA Illumina [715000] 5 treprostinil dose measurement http://www.ebi.ac.uk/efo/EFO_0021489 GCST90128472 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. COVID-19 3,742 European ancestry cases, 79,430 European ancestry controls, 1,118 Hispanic or Latin American cases, 10,349 Hispanic or Latin American controls, 513 African American or Afro-Caribbean cases, 5,248 African American or Afro-Caribbean controls NA Illumina [8187660] (imputed) 24 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90094644 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. COVID-19 (hospitalized vs not hospitalized) 337 European ancestry cases, 2,908 European ancestry controls, 80 Hispanic or Latin American cases, 886 Hispanic or Latin American controls, 57 African American or Afro-Caribbean cases, 365 African American or Afro-Caribbean controls NA Illumina [8187660] (imputed) 36 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90101882 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. COVID-19 (hospitalized vs population) 337 European ancestry cases, 82,347 European ancestry controls, 80 Hispanic or Latin American cases, 11,237 Hispanic or Latin American controls, 57 African American or Afro-Caribbean cases, 5,614 African American or Afro-Caribbean controls NA Illumina [8187660] (imputed) 47 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90094646 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. COVID-19 in household exposure to COVID-19 1,363 European ancestry cases, 707 European ancestry controls, 495 Hispanic or Latin American cases, 264 Hispanic or Latin American controls, 164 African American or Afro-Caribbean cases, 89 African American or Afro-Caribbean controls NA Illumina [8187660] (imputed) 9 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90094647 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. General population vs COVID-19 exposed negative controls 81,904 European ancestry cases, 707 European ancestry controls, 11,039 Hispanic or Latin American cases, 264 Hispanic or Latin American controls, 5,564 African American or Afro-Caribbean cases, 89 African American or Afro-Caribbean controls NA Illumina [8187660] (imputed) 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90094648 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. COVID-19 (symptomatic vs paucisymptomatic) 3,015 European ancestry cases, 268 European ancestry controls, 943 Hispanic or Latin American cases, 79 Hispanic or Latin American controls, 395 African American or Afro-Caribbean cases, 44 African American or Afro-Caribbean controls NA Illumina [8187660] (imputed) 50 COVID-19 symptoms measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0600019, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90094649 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. COVID-19 severity score 3,452 European ancestry individuals, 1,040 Hispanic or Latin American individuals, 460 African American or Afro-Caribbean individuals NA Illumina [8187660] (imputed) 22 COVID-19 symptoms measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0600019, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90094650 Genome-wide genotyping array 2022-04-22 35410379 Roberts GHL 2022-04-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35410379 Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects. COVID-19 (covid vs negative) 3,742 European ancestry cases, 28,145 European ancestry controls, 1,118 Hispanic or Latin American cases, 5,061 Hispanic or Latin American controls, 513 African American or Afro-Caribbean cases, 2,695 African American or Afro-Caribbean controls NA Illumina [8187660] (imputed) 24 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90094643 Genome-wide genotyping array 2022-06-16 35681050 Andreu-Sanchez S 2022-06-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35681050 Genetic, parental and lifestyle factors influence telomere length. Granulocyte telomere length 902 European ancestry individuals NA Illumina [5327634] (imputed) 12 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90101887 Genome-wide genotyping array 2022-06-16 35681050 Andreu-Sanchez S 2022-06-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35681050 Genetic, parental and lifestyle factors influence telomere length. Lymphocyte telomere length 902 European ancestry individuals NA Illumina [5327634] (imputed) 9 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90101888 Genome-wide genotyping array 2022-06-16 35681050 Andreu-Sanchez S 2022-06-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35681050 Genetic, parental and lifestyle factors influence telomere length. Naive T-cell telomere length 902 European ancestry individuals NA Illumina [5327634] (imputed) 9 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90101889 Genome-wide genotyping array 2022-06-16 35681050 Andreu-Sanchez S 2022-06-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35681050 Genetic, parental and lifestyle factors influence telomere length. Memory T-cell telomere length 902 European ancestry individuals NA Illumina [5327634] (imputed) 12 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90101890 Genome-wide genotyping array 2022-06-16 35681050 Andreu-Sanchez S 2022-06-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35681050 Genetic, parental and lifestyle factors influence telomere length. B-cell telomere length 902 European ancestry individuals NA Illumina [5327634] (imputed) 16 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90101891 Genome-wide genotyping array 2022-06-16 35681050 Andreu-Sanchez S 2022-06-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35681050 Genetic, parental and lifestyle factors influence telomere length. NK-cell telomere length 902 European ancestry individuals NA Illumina [5327634] (imputed) 10 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90101892 Genome-wide genotyping array 2022-03-15 34743297 Kulminski AM 2021-11-06 Geroscience www.ncbi.nlm.nih.gov/pubmed/34743297 Pleiotropic predisposition to Alzheimer's disease and educational attainment: insights from the summary statistics analysis. Alzheimer's disease or educational attainment (pleiotropy) (see Lambert 2013 and Okbay 2016) NA NR [6814003] 166 Alzheimer disease, educational attainment http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0011015 GCST90095190 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by chest pain in the last three months - 602 Bothered a lot (UKB data field 21052) 1,628 European ancestry cases, 153,480 European ancestry controls NA Affymetrix, Illumina [262627] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078799 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78: high cholesterol (Gene-based burden) 49,060 European ancestry cases, 279,992 European ancestry controls NA Illumina [184145] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90081870 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 500 Never (UKB data field 21034) 56,841 European ancestry cases, 98,245 European ancestry controls NA Affymetrix, Illumina [262595] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078727 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hypertension (Gene-based burden) 115,454 European ancestry cases, 216,300 European ancestry controls NA Illumina [184201] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90081631 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 501 Sometimes (UKB data field 21034) 72,063 European ancestry cases, 83,023 European ancestry controls NA Affymetrix, Illumina [262595] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078728 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I10: hypertension (Gene-based burden) 100,205 European ancestry cases, 228,845 European ancestry controls NA Illumina [184145] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90081632 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 502 Often (UKB data field 21034) 18,197 European ancestry cases, 136,889 European ancestry controls NA Affymetrix, Illumina [262595] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078729 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hyperthyroidism or thyrotoxicosis (Gene-based burden) 3,510 European ancestry cases, 328,244 European ancestry controls NA Illumina [184201] 0 hyperthyroidism, Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009189, http://www.ebi.ac.uk/efo/EFO_0009190 GCST90081714 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 503 Most of the time (UKB data field 21034) 6,888 European ancestry cases, 148,198 European ancestry controls NA Affymetrix, Illumina [262595] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078730 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05: Hyperthyroidism or thyrotoxicosis (Gene-based burden) 2,796 European ancestry cases, 326,256 European ancestry controls NA Illumina [184145] 0 hyperthyroidism, Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009189, http://www.ebi.ac.uk/efo/EFO_0009190 GCST90081715 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 504 Always (UKB data field 21034) 1,097 European ancestry cases, 153,989 European ancestry controls NA Affymetrix, Illumina [262595] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078731 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hypothyroidism or myxoedema (Gene-based burden) 22,064 European ancestry cases, 309,690 European ancestry controls NA Illumina [184201] 0 myxedema, hypothyroidism http://www.ebi.ac.uk/efo/EFO_1001055, http://www.ebi.ac.uk/efo/EFO_0004705 GCST90081716 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 500 Never (UKB data field 21033) 73,989 European ancestry cases, 81,088 European ancestry controls NA Affymetrix, Illumina [262592] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078722 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E03: Hypothyroidism or myxoedema (Gene-based burden) 18,362 European ancestry cases, 310,690 European ancestry controls NA Illumina [184145] 0 myxedema, hypothyroidism http://www.ebi.ac.uk/efo/EFO_1001055, http://www.ebi.ac.uk/efo/EFO_0004705 GCST90081717 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 501 Sometimes (UKB data field 21033) 61,495 European ancestry cases, 93,582 European ancestry controls NA Affymetrix, Illumina [262592] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078723 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Infectious mononucleosis glandular fever epstein barr virus ebv (Gene-based burden) 1,070 European ancestry cases, 330,684 European ancestry controls NA Illumina [184201] 0 infectious mononucleosis http://www.ebi.ac.uk/efo/EFO_0007326 GCST90081925 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 502 Often (UKB data field 21033) 12,932 European ancestry cases, 142,145 European ancestry controls NA Affymetrix, Illumina [262592] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078724 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B27: infectious mononucleosis glandular fever epstein barr virus ebv (Gene-based burden) 836 European ancestry cases, 328,216 European ancestry controls NA Illumina [184145] 0 infectious mononucleosis http://www.ebi.ac.uk/efo/EFO_0007326 GCST90081926 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 503 Most of the time (UKB data field 21033) 5,881 European ancestry cases, 149,196 European ancestry controls NA Affymetrix, Illumina [262592] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078725 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Infective viral hepatitis (Gene-based burden) 979 European ancestry cases, 330,775 European ancestry controls NA Illumina [184201] 0 viral human hepatitis infection http://www.ebi.ac.uk/efo/EFO_0004196 GCST90081688 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of hard lumpy stools in the last three months - 504 Always (UKB data field 21033) 780 European ancestry cases, 154,297 European ancestry controls NA Affymetrix, Illumina [262592] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078726 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B19: infective viral hepatitis (Gene-based burden) 861 European ancestry cases, 328,191 European ancestry controls NA Illumina [184145] 0 viral human hepatitis infection http://www.ebi.ac.uk/efo/EFO_0004196 GCST90081689 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by fainting spells in the last three months - 600 Not bothered at all (UKB data field 21054) 150,281 European ancestry cases, 4,808 European ancestry controls NA Affymetrix, Illumina [262589] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078803 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inguinal hernia (Gene-based burden) 2,528 European ancestry cases, 329,226 European ancestry controls NA Illumina [184201] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90081898 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by fainting spells in the last three months - 601 Bothered a little (UKB data field 21054) 4,538 European ancestry cases, 150,551 European ancestry controls NA Affymetrix, Illumina [262589] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078804 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-09-27 33875642 Duran-Lozano L 2021-04-19 Blood Cancer J www.ncbi.nlm.nih.gov/pubmed/33875642 Germline variants at SOHLH2 influence multiple myeloma risk. Multiple myeloma or monoclonal gammopathy of undetermined significance 4,376 European ancestry multiple myeloma cases, 944 European ancestry monoclonal gammopathy of undetermined significance cases, 422,293 European ancestry controls NA Illumina [33000000] (imputed) 1 multiple myeloma, monoclonal gammopathy http://www.ebi.ac.uk/efo/EFO_0001378, http://www.ebi.ac.uk/efo/EFO_0000203 GCST012397 Genome-wide genotyping array 2021-09-27 33875642 Duran-Lozano L 2021-04-19 Blood Cancer J www.ncbi.nlm.nih.gov/pubmed/33875642 Germline variants at SOHLH2 influence multiple myeloma risk. Multiple myeloma 4,376 European ancestry cases, 345,887 European ancestry controls 5,598 European ancestry cases, 15,261 European ancestry controls Illumina [33000000] (imputed) 13 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST012396 Genome-wide genotyping array 2021-05-18 33907307 Liu Y 2021-04-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/33907307 Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity. Neck circumference 13,625 European ancestry individuals, 1,465 African American individuals NA Affymetrix, Illumina [8865513] (imputed) 4 neck circumference http://www.ebi.ac.uk/efo/EFO_0011043 GCST90017133 Genome-wide genotyping array 2021-05-18 33907307 Liu Y 2021-04-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/33907307 Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity. Neck circumference 6,358 European and African American ancestry women NA Affymetrix, Illumina [7322639] (imputed) 3 neck circumference http://www.ebi.ac.uk/efo/EFO_0011043 GCST90017134 Genome-wide genotyping array 2021-05-18 33907307 Liu Y 2021-04-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/33907307 Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity. Neck circumference 8,732 European American and African American ancestry men NA Affymetrix, Illumina [7784259] (imputed) 5 neck circumference http://www.ebi.ac.uk/efo/EFO_0011043 GCST90017135 Genome-wide genotyping array 2021-05-18 33907307 Liu Y 2021-04-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/33907307 Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity. Neck circumference (BMI adjusted) 13,625 European ancestry individuals, 1,465 African American individuals 3,297 European ancestry individuals Affymetrix, Illumina [8865513] (imputed) 2 BMI-adjusted neck circumference http://www.ebi.ac.uk/efo/EFO_0011044 GCST90017136 Genome-wide genotyping array 2021-05-18 33907307 Liu Y 2021-04-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/33907307 Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity. Neck circumference (BMI adjusted) 6,358 European and African American ancestry women 1,743 European ancestry women Affymetrix, Illumina [7322639] (imputed) 0 BMI-adjusted neck circumference http://www.ebi.ac.uk/efo/EFO_0011044 GCST90017137 Genome-wide genotyping array 2021-05-18 33907307 Liu Y 2021-04-27 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/33907307 Genome-wide association study of neck circumference identifies sex-specific loci independent of generalized adiposity. Neck circumference (BMI adjusted) 8,732 European and African American ancestry men 1,554 European ancestry men Affymetrix, Illumina [7789444] (imputed) 1 BMI-adjusted neck circumference http://www.ebi.ac.uk/efo/EFO_0011044 GCST90017138 Genome-wide genotyping array 2021-09-08 33898419 Mukhopadhyay N 2021-04-09 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33898419 Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions. Nonsyndromic cleft lip with or without cleft palate 154 African ancestry cases, 274 African ancestry controls, 445 Asian ancestry cases, 1,246 Asian ancestry controls, 569 European ancestry cases, 2,704 European ancestry controls, 1,050 Central and South American cases, 2,988 Central and South American controls, 3 cases, 14 controls NA Illumina [NR] (imputed) 18 Orofacial cleft http://purl.obolibrary.org/obo/HP_0000202 GCST012337 Genome-wide genotyping array 2021-01-27 33444683 Chatterjee A 2021-01-11 Gene www.ncbi.nlm.nih.gov/pubmed/33444683 Exome-wide scan identifies significant association of rs4788084 in IL27 promoter with increase in hepatic fat content among Indians. Hepatic lipid content 244 Asian Indian individuals NA Illumina [726508] (imputed) 0 hepatic lipid content measurement http://www.ebi.ac.uk/efo/EFO_0006506 GCST010995 Exome genotyping array [Exome array] 2021-09-27 33939221 He X 2021-05-03 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/33939221 The morphometry of left cuneus mediating the genetic regulation on working memory. Left cuneus volume 753 European ancestry individuals, 301 individuals NA Illumina [11061864] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST012404 Genome-wide genotyping array 2021-05-19 33087363 Xu W 2020-10-21 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33087363 The FAM171A2 gene is a key regulator of progranulin expression and modifies the risk of multiple neurodegenerative diseases. Cerebrospinal fluid progranulin levels 432 European ancestry individuals 930 Han Chinese ancestry individuals Illumina [3262988] (imputed) 10 progranulin measurement http://www.ebi.ac.uk/efo/EFO_0004625 GCST011705 Genome-wide genotyping array 2021-09-27 33949668 Ma Y 2021-05-05 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33949668 Integrative Genomics Analysis Reveals a 21q22.11 Locus Contributing Risk to COVID-19. COVID-19 3,288 European ancestry cases, 676,840 European ancestry controls NA NR [8424883] (imputed) 3 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST012399 Genome-wide genotyping array 2021-09-06 33830993 Johnston KJA 2021-04-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33830993 Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank. Multisite chronic pain 178,556 British ancestry men NA NR [NR] (imputed) 5 multisite chronic pain http://www.ebi.ac.uk/efo/EFO_0010100 GCST012333 Genome-wide genotyping array 2021-09-06 33830993 Johnston KJA 2021-04-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33830993 Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank. Multisite chronic pain 387,649 British ancestry individuals NA NR [NR] (imputed) 87 multisite chronic pain http://www.ebi.ac.uk/efo/EFO_0010100 GCST012332 Genome-wide genotyping array 2021-09-06 33830993 Johnston KJA 2021-04-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33830993 Sex-stratified genome-wide association study of multisite chronic pain in UK Biobank. Multisite chronic pain 209,093 British ancestry women NA NR [NR] (imputed) 10 multisite chronic pain http://www.ebi.ac.uk/efo/EFO_0010100 GCST012334 Genome-wide genotyping array 2020-10-16 32527199 van Duijvenboden S 2020-06-11 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32527199 Genetic Basis and Prognostic Value of Exercise QT Dynamics. QT dynamics during exercise 28,449 European ancestry women, 24,412 European ancestry men NA Affymetrix [9800000] (imputed) 44 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90010359 Genome-wide genotyping array 2020-10-16 32527199 van Duijvenboden S 2020-06-11 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32527199 Genetic Basis and Prognostic Value of Exercise QT Dynamics. QT dynamics during recovery from exercise 51,503 European ancestry individuals NA Affymetrix [9800000] (imputed) 3 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90010360 Genome-wide genotyping array 2020-10-30 31566214 Kulminski AM 2019-09-30 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/31566214 Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids. High density lipoprotein cholesterol levels 29,902 European ancestry individuals NA Affymetrix, Illumina [up to 2500000] (imputed) 18 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90010361 Genome-wide genotyping array 2020-10-30 31566214 Kulminski AM 2019-09-30 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/31566214 Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids. Triglyceride levels 29,902 European ancestry individuals NA Affymetrix, Illumina [up to 2500000] (imputed) 13 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90010362 Genome-wide genotyping array 2020-10-30 31566214 Kulminski AM 2019-09-30 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/31566214 Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids. Total cholesterol levels 29,902 European ancestry individuals NA Affymetrix, Illumina [up to 2500000] (imputed) 24 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90010363 Genome-wide genotyping array 2020-10-30 31566214 Kulminski AM 2019-09-30 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/31566214 Quantitative and qualitative role of antagonistic heterogeneity in genetics of blood lipids. Low density lipoprotein cholesterol levels 29,902 European ancestry individuals Affymetrix, Illumina [up to 2500000] (imputed) 14 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90010364 Genome-wide genotyping array 2021-06-04 33203692 Labadie JD 2020-11-17 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/33203692 Genetic predictors of severe skin toxicity in stage III colon cancer patients treated with cetuximab: NCCTG N0147 (Alliance). Severe skin toxicity response to cetuximab in stage 3 colon cancer 216 European ancestry cases, 12 African ancestry cases, 9 Asian ancestry cases, 3 Oceanian ancestry cases, 3 cases, 819 European ancestry controls, 74 African ancestry controls, 51 Asian ancestry controls, 4 American Indian ancestry controls, 3 Oceanian ancestry controls, 15 controls NA Illumina [10574903] (imputed) 2 skin disease, colon carcinoma, response to cetuximab http://www.ebi.ac.uk/efo/EFO_0000701, http://www.ebi.ac.uk/efo/EFO_1001950, http://www.ebi.ac.uk/efo/EFO_0007682 GCST011795 Genome-wide genotyping array 2021-06-07 33203707 Zheng JS 2020-11-17 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/33203707 Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations. Vitamin C levels 52,018 European ancestry individuals NA Affymetrix, Illumina [up to 7933258] (imputed) 11 vitamin C measurement http://www.ebi.ac.uk/efo/EFO_0600003 GCST011816 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHB7 5,323 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090030 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGA1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089439 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGA10 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089350 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGA11 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089499 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGA12 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089583 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGA2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089708 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGA8 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086643 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGA8 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087894 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGB1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086878 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGB2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086454 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGB4 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086422 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGC3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089882 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHGC5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089965 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCNA 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088132 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCOLCE 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086629 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCOLCE2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089278 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCSK1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087415 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCSK1N 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090679 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCSK2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089287 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCSK7 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088697 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCSK9 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90088969 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCSK9 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90090076 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCYOX1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089422 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCYOX1L 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089083 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDCD1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090566 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDCD1LG2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088180 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDCD5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087041 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDCL2 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087830 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE11A 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088980 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE1A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088981 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE2A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088975 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE3A 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088982 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE4D 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088983 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE5A 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088984 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE6D 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087476 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE7A 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088954 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDE9A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088958 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFA 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088720 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088605 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFC 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087589 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFC 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088535 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFD 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090642 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFRA 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086244 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFRB 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088399 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDGFRL 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090782 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDIA3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088765 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDIA3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089864 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDIA4 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089693 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDIA4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089694 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDIA5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089079 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF43 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087798 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF8 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087900 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNGTT 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087266 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNPC3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087245 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNPEP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086949 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROBO1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089185 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROBO2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088937 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROBO3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088938 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROBO4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090569 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROCK2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087586 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROR1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087421 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROR1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087969 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROR1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090212 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROR2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089884 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RORB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087017 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RORC 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086869 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ROS1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090461 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPE 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087121 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPIA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086917 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPL30 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087013 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPLP2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086511 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPN1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086298 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPN1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089440 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPRD1A 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087498 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS10 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087336 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBN3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087849 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBP1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089736 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBP2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090873 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBXL4 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086733 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBXL4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087853 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBXL4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090909 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBXL4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090929 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBXL5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087265 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBXO3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087890 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCAMR 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090755 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCAR 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088847 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCER1A 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090585 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAPLN 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086640 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAPOLG 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090140 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAPPA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088604 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAPPA2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089200 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAPSS1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087712 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARK2 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087337 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARK7 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088873 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARK7 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090857 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARP1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086328 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARP1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090366 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARP11 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087290 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARP16 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089898 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PARVA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087440 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDIA6 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089122 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDILT 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089655 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089186 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089117 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE6 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089118 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE7 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089289 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASEH1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090211 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RND1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087536 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF114 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090934 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF122 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086578 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF128 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089468 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF128 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090243 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF13 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090041 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF146 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086728 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF148 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089798 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF148 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090932 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF149 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090816 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF150 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090817 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF165 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086797 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF215 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089812 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF215 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090483 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF24 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090765 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF34 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087413 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF41 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087427 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNF43 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086310 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PATE1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090173 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PATE4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090024 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAWR 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090753 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAX4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086957 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAXIP1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087296 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PBRM1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087042 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PC 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087702 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCBD1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086680 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCBD2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089556 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCBP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086757 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDH10 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090293 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDH10 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090452 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDH15 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087841 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDH8 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089335 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDH9 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086340 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHA4 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086327 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHA4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089702 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHA7 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090276 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHAC1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089723 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHAC2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090656 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHB1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090924 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHB10 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090938 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHB14 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086420 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHB2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086434 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PCDHB4 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086321 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM171A1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089090 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM171A2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087467 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM171B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090021 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM171B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090297 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM171B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090339 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM172A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089095 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM173A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089696 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM174A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089519 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM174B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090475 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM175A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090295 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM175B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090326 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM175B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090396 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM177A1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090005 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM189A2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089155 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM189A2 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089166 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM19A1 5,323 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089197 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM19A2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089421 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM19A3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089867 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM19A4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089469 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM19A5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089089 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM209B 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089641 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM20A 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089423 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM20B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089729 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM210A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087877 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM213A 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087432 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM234B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089907 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM234B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090945 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM24B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090289 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM3B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089097 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM3B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090536 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM3D 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087374 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM3D 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089922 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM69C 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087872 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM96A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090298 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FANCF 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086692 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FANCL 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086212 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAP 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088883 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FARS2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087671 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAS 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089027 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAS 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089320 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAS 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090559 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAS 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090701 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FASLG 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088208 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FASN 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090187 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FATE1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089796 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAXDC2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090489 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBL 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087706 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBLN1 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086461 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBLN1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089449 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FBLN5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086430 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS4 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088165 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS7 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090547 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS7B 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090683 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS8 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088805 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS9 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090548 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGI3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089977 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGMN 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088463 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGMN 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089868 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGR5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089672 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LHB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090164 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LHCGR 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087893 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIF 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089835 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIFR 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90089219 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRA3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089392 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRA4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090112 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRA5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089832 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRA5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090282 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRA6 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089637 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRB1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088913 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRB2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088914 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRB2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089109 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRB3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086691 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRB4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089435 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LILRB5 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089622 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIMA1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086786 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC32 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089774 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC37A2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090368 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC4B 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086882 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC4B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090906 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC4C 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090662 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC52 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086448 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC74A 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090176 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRK2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086528 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK2A2;CSNK2B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088964 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK2B 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086689 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSPG4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090402 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSRP2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087324 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSRP3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090531 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089041 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088663 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST3 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087977 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087762 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST4 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088517 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087592 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088518 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST6 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087915 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST6 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088301 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST7 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087734 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088300 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CST8 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086348 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRB1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086902 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CREB3L1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086603 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CREB3L3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090395 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CREB3L4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086676 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CREBBP 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087562 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CREG1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090652 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRELD1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089777 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRH 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089094 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRHBP 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089265 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRIM1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089463 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRIM1 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090266 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRIP2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090474 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRISP2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090605 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRISP3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088255 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRISPLD2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089149 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRK 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088838 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRKL 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090881 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRLF1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087917 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRLF2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087616 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRLF2 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088045 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CROT 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087661 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRP 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088668 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRTAC1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089108 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRTAM 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088898 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRTAM 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089957 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRIG3 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088314 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRIT2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086864 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRIT3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086779 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRIT3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086886 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRMP 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086414 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRMP 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090506 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090236 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090539 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP11 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089551 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP11 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090134 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP12 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089800 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP1B 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086653 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP1B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089779 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP2 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086370 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRP8 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088315 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRPAP1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088474 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRPAP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090325 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRPPRC 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086408 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRPPRC 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090470 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC15 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089496 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC19 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089621 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC24 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090950 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC25 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090627 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC25 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090949 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRC3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089566 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX6C 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090373 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX7A1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090177 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX7A2L 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090768 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX8A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086304 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPA2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090600 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPA4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090596 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPB1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089361 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPB2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088431 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPD 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089920 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPE 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089007 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPE 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089260 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPM 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089819 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPM 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090688 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPN1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089689 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPN2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089412 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPNE1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086817 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPNE1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089009 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPQ 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090681 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPT1B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086861 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPVL 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090364 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPXM1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089322 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CPZ 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089458 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRABP1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086894 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRABP2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086858 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRAT 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087117 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRYAA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086226 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRYBB2 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086175 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRYGD 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086936 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRYZ 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087697 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CRYZL1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090553 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSAG1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089164 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSDC2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087206 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSDE1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087194 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 colony stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010775 GCST90086431 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF1 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 colony stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010775 GCST90088502 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF1R 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087606 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF1R 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087998 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088757 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF2RA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086268 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF2RB 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086315 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF2RB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086560 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088782 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090403 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSF3R 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088033 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSGALNACT2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086445 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSH1;CSH2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087375 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSH2 5,324 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089308 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase CSK measurement http://www.ebi.ac.uk/efo/EFO_0020820 GCST90088343 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSMD1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090771 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSMD2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090942 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSN1S1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088755 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK1D 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086667 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK1G2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087127 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK2A1 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088380 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK2A1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088962 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK2A1;CSNK2B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088963 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSNK2A2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087605 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FRRS1L 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089961 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FRS2 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087341 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FRZB 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087651 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FRZB 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088099 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FSHB 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090002 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FST 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088590 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FSTL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087381 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FSTL1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090617 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FSTL3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088386 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FSTL4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090647 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FSTL5 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089659 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LEPR 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089028 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LEPR 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090754 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LETMD1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089195 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090012 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088194 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088218 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LGALS3BP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088859 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIN7B 5,320 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088636 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIN7C 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087329 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LINGO1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089531 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LINGO3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086464 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIPA 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089743 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIPF 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090649 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIPK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089410 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LIPN 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090049 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LMAN2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089778 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LMAN2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090706 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LMAN2L 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089985 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LMCD1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090738 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LMNB1 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088567 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LMOD1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087031 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LNX1 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090921 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LOC652493 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089498 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LONP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089396 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LOXL2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089464 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LPAL2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090579 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LPCAT2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086589 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LPO 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088774 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRCH4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086639 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRFN1 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089916 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRFN2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089731 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRFN5 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089515 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA6A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089940 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA6B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088940 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA6C 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087878 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA6C 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089733 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA7A 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089625 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMG1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089667 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMG2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089376 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SENP7 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087108 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEPHS1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087768 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEPT10 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087156 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEPT11 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087103 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERAC1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090428 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERF1A 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089870 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088440 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087387 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA10 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089512 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA11 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090440 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA12 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089492 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA3 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088122 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA3;KLK3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088609 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA3;KLK3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088665 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087787 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088394 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA5 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088356 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA6 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088772 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARA5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086257 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARB2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088923 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARF1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088945 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARF2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088946 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARF2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090407 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARF2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090911 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCG2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090165 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCG3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089949 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCGB1A1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086346 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCGB1C2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089248 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCGB1D2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089467 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCGB2A1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088860 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCGB2A1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090498 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCGB3A1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089321 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCGN 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086489 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCIMP 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086313 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCIN 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087150 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCMH1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087096 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCN2B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090147 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCN4B 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089917 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCO1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089878 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCP2D1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087827 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCT 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088498 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCUBE1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090430 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SDF2L1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089605 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA7 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088028 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINA9 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089771 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINB1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086429 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINC1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088329 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPIND1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088310 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINE1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088134 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINE2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088277 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINF1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089792 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINF1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090554 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINF2 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088186 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPING1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087626 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPING1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088708 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINH1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086452 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SERPINI2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089669 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SET 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 protein set measurement http://www.ebi.ac.uk/efo/EFO_0020688 GCST90089024 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SETD2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087122 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SETMAR 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087004 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEZ6L2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088556 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SF1 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087220 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SF3B4 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087447 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFN 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088778 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFRP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087737 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFRP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088280 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFRP2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089805 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFRP4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090607 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFTA2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086352 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFTPB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086401 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFTPC 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089183 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFTPD 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088682 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SFXN5 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087642 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SGCB 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089627 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SGF29 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087228 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SGK3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086200 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SGTA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088557 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SH2D1A 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088747 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SH2D3C 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087170 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SH3BGRL 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087159 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SH3BP2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089820 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SH3GL2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087027 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHANK1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087403 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHANK1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087405 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHANK3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087404 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHBG 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90088820 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHBG 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90089915 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHC1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088993 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHC2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087761 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHC4 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086857 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHH 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088043 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHISA2 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086274 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHISA3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089636 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SDHAF2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089416 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEC11C 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086390 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEC13 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087908 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEC22A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087629 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEC61B 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089895 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEC61G 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090353 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SECTM1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087368 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEL1L2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090496 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SELE 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088403 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SELL 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088779 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SELP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088610 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SELPLG 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086649 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SELPLG 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089594 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA3A 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088281 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA3B 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089135 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA3C 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089432 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA3E 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086399 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA3E 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089023 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA3G 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089104 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA4B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090834 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA4C 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089926 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA4D 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089182 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA4F 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090918 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA5A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087396 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SEMA6A 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088941 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SKIL 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087901 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SKP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088577 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLAMF1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 signaling lymphocytic activation molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010794 GCST90089946 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLAMF6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088944 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLAMF7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089059 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLAMF7 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089899 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLAMF8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090435 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC14A1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087437 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC14A2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087248 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC16A3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090471 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC22A16 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090940 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC25A18 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088995 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC26A11 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087487 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC26A5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090526 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC26A7 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087695 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC27A2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090469 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC30A3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090495 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC30A5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090769 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC35B3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086392 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC35G2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087486 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC3A1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090439 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC3A2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086265 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC3A2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089635 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC41A2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087036 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC4A8 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087234 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A4 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087797 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090798 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A5 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087838 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A6 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087367 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089239 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A7 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089919 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A9 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089005 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A9 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089850 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100P 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090912 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SAA1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088667 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SAMHD1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086674 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SAP18 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087255 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SAP30 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087292 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SARS2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086925 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SAT1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090869 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SAT2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087045 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SATB1 5,322 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087494 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SATB2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086222 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SAYSD1 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089518 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SBDS 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ribosome maturation protein sbds measurement http://www.ebi.ac.uk/efo/EFO_0020711 GCST90088555 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SBSN 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089170 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCAMP5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087492 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARA3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086479 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARA3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087304 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SCARA3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090788 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture finger (Gene-based burden) 798 European ancestry cases, 330,956 European ancestry controls NA Illumina [184201] 0 finger fracture http://www.ebi.ac.uk/efo/EFO_0009616 GCST90081960 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maternal age (UKB data field 1845) 167,682 European ancestry individuals NA Affymetrix, Illumina [280752] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90077616 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S6260: fracture finger (Gene-based burden) 683 European ancestry cases, 328,369 European ancestry controls NA Illumina [184145] 0 finger fracture http://www.ebi.ac.uk/efo/EFO_0009616 GCST90081961 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50: Other and unspecified disorders of male genital organs 5,205 European ancestry cases, 164,191 European ancestry controls NA Affymetrix, Illumina [280133] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90080635 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture of forearm or wrist (Gene-based burden) 1,206 European ancestry cases, 330,548 European ancestry controls NA Illumina [184201] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90081956 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oral contraceptive pill last use (age of onset) (UKB data field 2804) 169,064 European ancestry individuals NA Affymetrix, Illumina [279821] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078961 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52: Fracture of forearm or wrist (Gene-based burden) 997 European ancestry cases, 328,055 European ancestry controls NA Illumina [184145] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90081957 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankle spacing width right (UKB data field 4119) 166,358 European ancestry individuals NA Affymetrix, Illumina [278841] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90079154 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture lower leg ankle (Gene-based burden) 2,253 European ancestry cases, 329,501 European ancestry controls NA Illumina [184201] 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90081964 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density T score automated right (UKB data field 4125) 166,358 European ancestry individuals NA Affymetrix, Illumina [278841] 1 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90079159 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82: fracture lower leg ankle (Gene-based burden) 1,803 European ancestry cases, 327,249 European ancestry controls NA Illumina [184145] 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90081965 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel quantitative ultrasound index direct entry right (UKB data field 4123) 166,358 European ancestry individuals NA Affymetrix, Illumina [278841] 1 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90079157 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture nose (Gene-based burden) 744 European ancestry cases, 331,010 European ancestry controls NA Illumina [184201] 0 nose injury http://www.ebi.ac.uk/efo/EFO_0009623 GCST90081950 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of sound through heel right (UKB data field 4122) 166,358 European ancestry individuals NA Affymetrix, Illumina [278841] 1 velocity of sound measurement http://www.ebi.ac.uk/efo/EFO_0005654 GCST90079156 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S022: fracture nose (Gene-based burden) 626 European ancestry cases, 328,426 European ancestry controls NA Illumina [184145] 0 nose injury http://www.ebi.ac.uk/efo/EFO_0009623 GCST90081951 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel broadband ultrasound attenuation right (UKB data field 4120) 166,349 European ancestry individuals NA Affymetrix, Illumina [278832] 1 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90079155 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture rib (Gene-based burden) 651 European ancestry cases, 331,103 European ancestry controls NA Illumina [184201] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90081962 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankle spacing width left (UKB data field 4100) 166,283 European ancestry individuals NA Affymetrix, Illumina [278781] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90079148 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S223: fracture rib (Gene-based burden) 571 European ancestry cases, 328,481 European ancestry controls NA Illumina [184145] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90081963 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density T score automated left (UKB data field 4106) 166,283 European ancestry individuals NA Affymetrix, Illumina [278781] 1 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90079153 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture tibia (Gene-based burden) 693 European ancestry cases, 331,061 European ancestry controls NA Illumina [184201] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90081966 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel quantitative ultrasound index direct entry left (UKB data field 4104) 166,283 European ancestry individuals NA Affymetrix, Illumina [278781] 1 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90079151 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S8220: fracture tibia (Gene-based burden) 597 European ancestry cases, 328,455 European ancestry controls NA Illumina [184145] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90081967 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of sound through heel left (UKB data field 4103) 166,283 European ancestry individuals NA Affymetrix, Illumina [278781] 1 velocity of sound measurement http://www.ebi.ac.uk/efo/EFO_0005654 GCST90079150 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture toe (Gene-based burden) 557 European ancestry cases, 331,197 European ancestry controls NA Illumina [184201] 0 foot fracture http://www.ebi.ac.uk/efo/EFO_0009618 GCST90081970 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by back pain in the past three months - 601 Bothered a little (UKB data field 21048) 72,655 European ancestry cases, 82,484 European ancestry controls NA Affymetrix, Illumina [262673] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078786 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gout (Gene-based burden) 6,554 European ancestry cases, 325,200 European ancestry controls NA Illumina [184201] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90081863 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by back pain in the past three months - 602 Bothered a lot (UKB data field 21048) 21,697 European ancestry cases, 133,442 European ancestry controls NA Affymetrix, Illumina [262673] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078787 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10: Gout (Gene-based burden) 5,396 European ancestry cases, 323,656 European ancestry controls NA Illumina [184145] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90081864 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling heart pound race in the last three months - 600 Not bothered at all (UKB data field 21055) 107,650 European ancestry cases, 47,487 European ancestry controls NA Affymetrix, Illumina [262660] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078805 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gynaecological disorder (not cancer) (Gene-based burden) 748 European ancestry cases, 331,006 European ancestry controls NA Illumina [184187] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90081777 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling heart pound race in the last three months - 601 Bothered a little (UKB data field 21055) 42,543 European ancestry cases, 112,594 European ancestry controls NA Affymetrix, Illumina [262660] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078806 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94: gynaecological disorder (not cancer) (Gene-based burden) 664 European ancestry cases, 177,230 European ancestry controls NA Illumina [177166] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90081778 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling heart pound race in the last three months - 602 Bothered a lot (UKB data field 21055) 4,944 European ancestry cases, 150,193 European ancestry controls NA Affymetrix, Illumina [262660] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078807 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Haemorrhoids piles (Gene-based burden) 1,601 European ancestry cases, 330,153 European ancestry controls NA Illumina [184201] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90081891 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by shortness of breath in the last three months - 600 Not bothered at all (UKB data field 21056) 106,502 European ancestry cases, 48,638 European ancestry controls NA Affymetrix, Illumina [262659] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078808 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64: haemorrhoids piles (Gene-based burden) 1,291 European ancestry cases, 327,761 European ancestry controls NA Illumina [184145] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90081892 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by shortness of breath in the last three months - 601 Bothered a little (UKB data field 21056) 42,621 European ancestry cases, 112,519 European ancestry controls NA Affymetrix, Illumina [262659] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078809 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hayfever allergic rhinitis (Gene-based burden) 27,391 European ancestry cases, 304,363 European ancestry controls NA Illumina [184201] 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90081801 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by shortness of breath in the last three months - 602 Bothered a lot (UKB data field 21056) 6,017 European ancestry cases, 149,123 European ancestry controls NA Affymetrix, Illumina [262659] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078810 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30: hayfever allergic rhinitis (Gene-based burden) 21,078 European ancestry cases, 307,974 European ancestry controls NA Illumina [184145] 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90081802 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by nausea in the last three months - 600 Not bothered at all (UKB data field 21059) 131,651 European ancestry cases, 23,472 European ancestry controls NA Affymetrix, Illumina [262648] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078817 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Head injury (Gene-based burden) 1,488 European ancestry cases, 330,266 European ancestry controls NA Illumina [184201] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90081733 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by nausea in the last three months - 601 Bothered a little (UKB data field 21059) 21,760 European ancestry cases, 133,363 European ancestry controls NA Affymetrix, Illumina [262648] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078818 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Headaches (not migraine) (Gene-based burden) 3,962 European ancestry cases, 327,792 European ancestry controls NA Illumina [184201] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90081830 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by nausea in the last three months - 602 Bothered a lot (UKB data field 21059) 1,712 European ancestry cases, 153,411 European ancestry controls NA Affymetrix, Illumina [262648] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078819 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R51: headaches (not migraine) (Gene-based burden) 3,285 European ancestry cases, 325,767 European ancestry controls NA Illumina [184145] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90081831 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain in arms legs joints in the past three months - 600 Not bothered at all (UKB data field 21049) 42,914 European ancestry cases, 112,199 European ancestry controls NA Affymetrix, Illumina [262645] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078788 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart arrhythmia (Gene-based burden) 2,496 European ancestry cases, 329,258 European ancestry controls NA Illumina [184201] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90081645 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain in arms legs joints in the past three months - 601 Bothered a little (UKB data field 21049) 79,690 European ancestry cases, 75,423 European ancestry controls NA Affymetrix, Illumina [262645] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078789 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pravastatin 2,500 European ancestry cases, 318,258 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078132 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z74.1: Need for assistance with personal care (Gene-based burden) 584 European ancestry cases, 385,416 European ancestry controls NA Illumina [185295] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085304 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prednisolone 2,671 European ancestry cases, 318,087 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078076 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z75: Problems related to medical facilities and other health care (Gene-based burden) 1,492 European ancestry cases, 385,407 European ancestry controls NA Illumina [185330] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085307 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pregabalin 1,076 European ancestry cases, 319,682 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078231 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z75.1: Person awaiting admission to adequate facility elsewhere (Gene-based burden) 988 European ancestry cases, 386,207 European ancestry controls NA Illumina [185330] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085306 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prochlorperazine 621 European ancestry cases, 320,137 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078043 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z76: Persons encountering health services in other circumstances (Gene-based burden) 5,561 European ancestry cases, 374,354 European ancestry controls NA Illumina [185187] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085309 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - propranolol 3,052 European ancestry cases, 317,706 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078098 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z76.0: Encounter for issue of repeat prescription (Gene-based burden) 4,934 European ancestry cases, 376,664 European ancestry controls NA Illumina [185218] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085308 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prozac 597 European ancestry cases, 320,161 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078040 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79: Long term (current) drug therapy (Gene-based burden) 5,865 European ancestry cases, 375,980 European ancestry controls NA Illumina [185260] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085314 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pulmicort ls inhaler 675 European ancestry cases, 320,083 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078018 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.8: Other long term (current) drug therapy (Gene-based burden) 5,294 European ancestry cases, 377,396 European ancestry controls NA Illumina [185269] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085313 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - quinine 3,027 European ancestry cases, 317,731 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078071 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.84: Long term (current) use of oral hypoglycemic drugs (Gene-based burden) 3,574 European ancestry cases, 383,035 European ancestry controls NA Illumina [185320] 0 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90085310 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - qvar 50 inhaler 1,741 European ancestry cases, 319,017 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078196 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.89: Other long term (current) drug therapy (Gene-based burden) 1,743 European ancestry cases, 382,184 European ancestry controls NA Illumina [185292] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085312 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rabeprazole sodium 792 European ancestry cases, 319,966 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078200 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.890.: Hormone replacement therapy (Gene-based burden) 1,698 European ancestry cases, 382,280 European ancestry controls NA Illumina [185236] 0 hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0003961 GCST90085311 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ramipril 21,735 European ancestry cases, 299,023 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90077999 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80: Family history of primary malignant neoplasm (Gene-based burden) 13,831 European ancestry cases, 364,232 European ancestry controls NA Illumina [185195] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90085320 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ranitidine 7,746 European ancestry cases, 313,012 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078083 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.0: Family history of malignant neoplasm of digestive organs (Gene-based burden) 9,455 European ancestry cases, 376,016 European ancestry controls NA Illumina [185311] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90085315 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40: Glaucoma (Gene-based burden) 4,377 European ancestry cases, 324,675 European ancestry controls NA Illumina [184145] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90081741 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - migraleve tablet 588 European ancestry cases, 320,170 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078199 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56.6: Other physical and mental strain related to work (Gene-based burden) 1,484 European ancestry cases, 383,319 European ancestry controls NA Illumina [185297] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085279 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mirtazapine 1,305 European ancestry cases, 319,453 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078183 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56.8: Other problems related to employment (Gene-based burden) 5,671 European ancestry cases, 371,701 European ancestry controls NA Illumina [185165] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085281 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mometasone 939 European ancestry cases, 319,819 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078122 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56.89: Other problems related to employment (Gene-based burden) 5,671 European ancestry cases, 371,702 European ancestry controls NA Illumina [185165] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085280 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - montelukast product 897 European ancestry cases, 319,861 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078188 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z57: Occupational exposure to risk factors (Gene-based burden) 734 European ancestry cases, 387,125 European ancestry controls NA Illumina [185343] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90085283 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - movicol oral powder 1,431 European ancestry cases, 319,327 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078165 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z60: Problems related to social environment (Gene-based burden) 4,391 European ancestry cases, 382,712 European ancestry controls NA Illumina [185329] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085285 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - multivitamin mineral preparations 6,375 European ancestry cases, 314,383 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078081 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z60.2: Problems related to living alone (Gene-based burden) 4,286 European ancestry cases, 383,078 European ancestry controls NA Illumina [185333] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085284 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - multivitamins 14,139 European ancestry cases, 306,619 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90077996 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63: Other problems related to primary support group, including family circumstances (Gene-based burden) 4,579 European ancestry cases, 365,694 European ancestry controls NA Illumina [184995] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085290 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - naproxen 3,379 European ancestry cases, 317,379 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078065 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.4: Disappearance and death of family member (Gene-based burden) 2,457 European ancestry cases, 376,692 European ancestry controls NA Illumina [185163] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085286 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nasonex aqueous nasal spray 2,274 European ancestry cases, 318,484 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078181 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.7: Other stressful life events affecting family and household (Gene-based burden) 984 European ancestry cases, 384,233 European ancestry controls NA Illumina [185288] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085288 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nexium 769 European ancestry cases, 319,989 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078211 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.79: Other stressful life events affecting family and household (Gene-based burden) 890 European ancestry cases, 384,338 European ancestry controls NA Illumina [185288] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085287 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nicorandil 1,420 European ancestry cases, 319,338 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078141 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.8: Other specified problems related to primary support group (Gene-based burden) 610 European ancestry cases, 382,523 European ancestry controls NA Illumina [185257] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085289 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nifedipine 1,016 European ancestry cases, 319,742 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078002 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71: Persons encountering health services for other counseling and medical advice, not elsewhere classified (Gene-based burden) 58,197 European ancestry cases, 290,856 European ancestry controls NA Illumina [184652] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085295 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - olanzapine 501 European ancestry cases, 320,257 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078171 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evening primrose oil product 992 European ancestry cases, 319,766 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078237 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.41: Encounter for surveillance of contraceptive pills (Gene-based burden) 616 European ancestry cases, 386,850 European ancestry controls NA Illumina [185222] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085222 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evorel 25 patch 696 European ancestry cases, 320,062 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078152 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.43: Encounter for surveillance of intrauterine contraceptive device (Gene-based burden) 656 European ancestry cases, 385,702 European ancestry controls NA Illumina [185322] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085223 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ezetimibe 2,675 European ancestry cases, 318,083 European ancestry controls NA Affymetrix, Illumina [447992] 2 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078226 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.5: Surveillance of (intrauterine) contraceptive device (Gene-based burden) 1,304 European ancestry cases, 227,830 European ancestry controls NA Illumina [180826] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085225 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ezetrol 843 European ancestry cases, 319,915 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078227 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.8: Encounter for other contraceptive management (Gene-based burden) 842 European ancestry cases, 208,240 European ancestry controls NA Illumina [179780] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085226 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - felodipine 3,832 European ancestry cases, 316,926 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078131 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z33: Pregnant state (Gene-based burden) 1,929 European ancestry cases, 207,444 European ancestry controls NA Illumina [179761] 0 pregnancy http://www.ebi.ac.uk/efo/EFO_0002950 GCST90085228 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ferrous sulphate 2,261 European ancestry cases, 318,497 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078054 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z34: Encounter for supervision of normal pregnancy (Gene-based burden) 2,526 European ancestry cases, 208,571 European ancestry controls NA Illumina [179897] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085231 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fexofenadine 1,530 European ancestry cases, 319,228 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078179 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z34.8: Encounter for supervision of other normal pregnancy (Gene-based burden) 782 European ancestry cases, 210,963 European ancestry controls NA Illumina [179876] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085229 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flax oil 731 European ancestry cases, 320,027 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078145 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z34.9: Encounter for supervision of normal pregnancy, unspecified (Gene-based burden) 810 European ancestry cases, 210,819 European ancestry controls NA Illumina [179922] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085230 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flecainide 755 European ancestry cases, 320,003 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078130 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z35: Supervision of high-risk pregnancy (Gene-based burden) 1,111 European ancestry cases, 228,023 European ancestry controls NA Illumina [180752] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085232 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flixonase aqueous nasal spray 1,837 European ancestry cases, 318,921 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078079 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z36: Encounter for antenatal screening of mother (Gene-based burden) 1,858 European ancestry cases, 209,616 European ancestry controls NA Illumina [179915] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085234 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flixotide inhaler 747 European ancestry cases, 320,011 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078024 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z36.8: Encounter for other antenatal screening (Gene-based burden) 622 European ancestry cases, 211,111 European ancestry controls NA Illumina [179914] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085233 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fluoxetine 5,309 European ancestry cases, 315,449 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078088 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z37: Outcome of delivery (Gene-based burden) 13,034 European ancestry cases, 197,840 European ancestry controls NA Illumina [179876] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90085237 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fluticasone 2,123 European ancestry cases, 318,635 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078121 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lactulose product 1,198 European ancestry cases, 319,560 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078034 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51: Encounter for other aftercare and medical care (Gene-based burden) 34,913 European ancestry cases, 348,833 European ancestry controls NA Illumina [185277] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085272 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lansoprazole 16,815 European ancestry cases, 303,943 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078025 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.0: Encounter for antineoplastic radiation therapy (Gene-based burden) 2,775 European ancestry cases, 385,155 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085264 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - latanoprost 1,062 European ancestry cases, 319,696 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078176 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.1: Encounter for antineoplastic chemotherapy and immunotherapy (Gene-based burden) 12,171 European ancestry cases, 375,755 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085265 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lercanidipine 1,219 European ancestry cases, 319,539 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078185 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.2: Other chemotherapy (Gene-based burden) 12,384 European ancestry cases, 375,546 European ancestry controls NA Illumina [185344] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085266 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - levothyroxine sodium 19,017 European ancestry cases, 301,741 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078224 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.3: Blood transfusion without reported diagnosis (Gene-based burden) 1,195 European ancestry cases, 386,735 European ancestry controls NA Illumina [185344] 0 blood transfusion http://www.ebi.ac.uk/efo/EFO_0020988 GCST90085267 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lipitor 3,244 European ancestry cases, 317,514 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078175 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.4: Preparatory care for subsequent treatment, not elsewhere classified (Gene-based burden) 1,733 European ancestry cases, 386,197 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085268 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lisinopril 12,532 European ancestry cases, 308,226 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90077998 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.5: Encounter for palliative care (Gene-based burden) 5,496 European ancestry cases, 382,396 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085269 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - loperamide 1,496 European ancestry cases, 319,262 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078086 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.8: Encounter for other specified aftercare (Gene-based burden) 7,356 European ancestry cases, 376,032 European ancestry controls NA Illumina [185273] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085271 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - loratadine 3,386 European ancestry cases, 317,372 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078020 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.81: Encounter for therapeutic drug level monitoring (Gene-based burden) 6,041 European ancestry cases, 377,379 European ancestry controls NA Illumina [185274] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085270 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - losartan 4,692 European ancestry cases, 316,066 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078150 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53: Persons encountering health services for specific procedures and treatment, not carried out (Gene-based burden) 42,753 European ancestry cases, 320,965 European ancestry controls NA Illumina [184898] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085278 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mebeverine 2,282 European ancestry cases, 318,476 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078084 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.0: Procedure and treatment not carried out because of contraindication (Gene-based burden) 11,131 European ancestry cases, 374,692 European ancestry controls NA Illumina [185294] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085274 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - meloxicam 1,254 European ancestry cases, 319,504 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078168 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.09: Procedure and treatment not carried out because of other contraindication (Gene-based burden) 1,754 European ancestry cases, 383,927 European ancestry controls NA Illumina [185294] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085273 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - metformin 11,579 European ancestry cases, 309,179 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078119 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.2: Immunization not carried out because of patient decision for other and unspecified reason (Gene-based burden) 3,919 European ancestry cases, 376,013 European ancestry controls NA Illumina [185196] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085212 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diprobase cream 742 European ancestry cases, 320,016 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078082 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.20: Immunization not carried out because of patient decision for unspecified reason (Gene-based burden) 2,143 European ancestry cases, 382,081 European ancestry controls NA Illumina [185269] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085210 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dipyridamole 814 European ancestry cases, 319,944 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078005 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.21: Immunization not carried out because of patient refusal (Gene-based burden) 1,818 European ancestry cases, 381,550 European ancestry controls NA Illumina [185259] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085211 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - domperidone 908 European ancestry cases, 319,850 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078085 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.3: Underimmunization status (Gene-based burden) 2,689 European ancestry cases, 378,103 European ancestry controls NA Illumina [185220] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085213 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dosulepin 1,535 European ancestry cases, 319,223 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078139 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z29: Encounter for other prophylactic measures (Gene-based burden) 916 European ancestry cases, 386,945 European ancestry controls NA Illumina [185341] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085215 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dovobet ointment 536 European ancestry cases, 320,222 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078213 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30: Encounter for contraceptive management (Gene-based burden) 14,142 European ancestry cases, 184,313 European ancestry controls NA Illumina [179016] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085227 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - doxazosin 5,111 European ancestry cases, 315,647 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078093 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.0: Encounter for general counseling and advice on contraception (Gene-based burden) 4,439 European ancestry cases, 202,477 European ancestry controls NA Illumina [179630] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085219 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - enalapril 3,349 European ancestry cases, 317,409 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078128 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.01: Encounter for initial prescription of contraceptives (Gene-based burden) 1,304 European ancestry cases, 385,278 European ancestry controls NA Illumina [185317] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085217 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - epilim 701 European ancestry cases, 320,057 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078067 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.011.: Encounter for initial prescription of contraceptive pills (Gene-based burden) 1,215 European ancestry cases, 385,879 European ancestry controls NA Illumina [185324] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085216 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - escitalopram 807 European ancestry cases, 319,951 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078215 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.09: Encounter for other general counseling and advice on contraception (Gene-based burden) 3,230 European ancestry cases, 380,302 European ancestry controls NA Illumina [185276] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085218 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - esomeprazole 1,565 European ancestry cases, 319,193 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078210 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.1: Insertion of (intrauterine) contraceptive device (Gene-based burden) 1,026 European ancestry cases, 228,108 European ancestry controls NA Illumina [180826] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085220 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - estradiol product 888 European ancestry cases, 319,870 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078216 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.2: Encounter for sterilization (Gene-based burden) 2,861 European ancestry cases, 207,343 European ancestry controls NA Illumina [179810] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085221 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evening primrose oil 6,997 European ancestry cases, 313,761 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078151 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.4: Encounter for surveillance of contraceptives (Gene-based burden) 1,670 European ancestry cases, 382,887 European ancestry controls NA Illumina [185295] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085224 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z46: Encounter for fitting and adjustment of other devices (Gene-based burden) 6,157 European ancestry cases, 381,771 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085252 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gtn spray 1,101 European ancestry cases, 319,657 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90077994 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z46.6: Encounter for fitting and adjustment of urinary device (Gene-based burden) 5,605 European ancestry cases, 382,323 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085251 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gtn glyceryl trinitrate 776 European ancestry cases, 319,982 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078163 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z47: Orthopedic aftercare (Gene-based burden) 3,988 European ancestry cases, 383,942 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085254 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - hydroxychloroquine 691 European ancestry cases, 320,067 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078113 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z47.0: Follow-up care involving removal of fracture plate and other internal fixation device (Gene-based burden) 3,640 European ancestry cases, 384,290 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085253 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - hypromellose 808 European ancestry cases, 319,950 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078078 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z48: Encounter for other postprocedural aftercare (Gene-based burden) 1,761 European ancestry cases, 386,128 European ancestry controls NA Illumina [185342] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085257 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ibuprofen 56,585 European ancestry cases, 264,173 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078064 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z48.0: Encounter for attention to dressings, sutures and drains (Gene-based burden) 564 European ancestry cases, 387,356 European ancestry controls NA Illumina [185342] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085255 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - imigran 747 European ancestry cases, 320,011 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078142 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z48.8: Encounter for other specified postprocedural aftercare (Gene-based burden) 970 European ancestry cases, 386,929 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085256 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - indapamide 1,602 European ancestry cases, 319,156 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078035 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50: Care involving use of rehabilitation procedures (Gene-based burden) 5,250 European ancestry cases, 382,680 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085263 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - insulin product 4,350 European ancestry cases, 316,408 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078106 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.0: Cardiac rehabilitation (Gene-based burden) 686 European ancestry cases, 387,244 European ancestry controls NA Illumina [185344] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085258 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ipratropium 552 European ancestry cases, 320,206 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078109 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.1: Other physical therapy (Gene-based burden) 2,855 European ancestry cases, 385,075 European ancestry controls NA Illumina [185344] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085259 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - irbesartan 3,196 European ancestry cases, 317,562 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078184 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.7: Occupational therapy and vocational rehabilitation, not elsewhere classified (Gene-based burden) 1,235 European ancestry cases, 386,695 European ancestry controls NA Illumina [185344] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085260 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - iron product 1,367 European ancestry cases, 319,391 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078125 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.8: Care involving use of other rehabilitation procedures (Gene-based burden) 669 European ancestry cases, 387,261 European ancestry controls NA Illumina [185344] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085261 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lacri lube eye ointment 679 European ancestry cases, 320,079 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078100 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.9: Care involving use of rehabilitation procedure, unspecified (Gene-based burden) 906 European ancestry cases, 387,024 European ancestry controls NA Illumina [185344] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90085262 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.2: Person consulting for explanation of examination or test findings (Gene-based burden) 11,120 European ancestry cases, 364,626 European ancestry controls NA Illumina [185180] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085291 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - olmesartan 532 European ancestry cases, 320,226 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078229 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.3: Dietary counseling and surveillance (Gene-based burden) 7,443 European ancestry cases, 365,535 European ancestry controls NA Illumina [185066] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085292 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - omega 3 fish oil supplement 17,260 European ancestry cases, 303,498 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078235 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.8: Other specified counseling (Gene-based burden) 675 European ancestry cases, 387,017 European ancestry controls NA Illumina [185344] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085293 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - omeprazole 28,675 European ancestry cases, 292,083 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078032 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.9: Counseling, unspecified (Gene-based burden) 46,702 European ancestry cases, 313,285 European ancestry controls NA Illumina [184866] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085294 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - orlistat 512 European ancestry cases, 320,246 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078201 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72: Problems related to lifestyle (Gene-based burden) 41,581 European ancestry cases, 316,106 European ancestry controls NA Illumina [184781] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085301 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - oxybutynin 1,071 European ancestry cases, 319,687 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078110 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.0: Tobacco use (Gene-based burden) 21,842 European ancestry cases, 355,170 European ancestry controls NA Illumina [185162] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90085296 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - oxytetracycline 1,287 European ancestry cases, 319,471 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078070 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.1: Alcohol use (Gene-based burden) 10,125 European ancestry cases, 377,805 European ancestry controls NA Illumina [185344] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085297 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pantoprazole 843 European ancestry cases, 319,915 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078172 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.3: Lack of physical exercise (Gene-based burden) 867 European ancestry cases, 383,244 European ancestry controls NA Illumina [185283] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085298 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - paracetamol 83,776 European ancestry cases, 236,982 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078241 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.8: Other problems related to lifestyle (Gene-based burden) 11,329 European ancestry cases, 357,964 European ancestry controls NA Illumina [185000] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085300 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - paroxetine 1,461 European ancestry cases, 319,297 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078042 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.89: Other problems related to lifestyle (Gene-based burden) 11,281 European ancestry cases, 358,061 European ancestry controls NA Illumina [185000] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085299 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - perindopril 6,331 European ancestry cases, 314,427 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078129 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z73: Problems related to life management difficulty (Gene-based burden) 1,198 European ancestry cases, 384,766 European ancestry controls NA Illumina [185310] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085302 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pioglitazone 917 European ancestry cases, 319,841 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078203 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z74: Problems related to care provider dependency (Gene-based burden) 1,224 European ancestry cases, 384,269 European ancestry controls NA Illumina [185276] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085305 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - piriton 684 European ancestry cases, 320,074 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078019 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z74.0: Reduced mobility (Gene-based burden) 500 European ancestry cases, 386,867 European ancestry controls NA Illumina [185325] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085303 Exome-wide sequencing 2021-07-27 33959940 Chen Y 2021-05-06 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/33959940 A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans. Facial wrinkles (forehead) 6,254 Latin American individuals NA Illumina [8703729] (imputed) 4 Facial wrinkling http://purl.obolibrary.org/obo/HP_0009762 GCST012109 Genome-wide genotyping array 2021-07-27 33959940 Chen Y 2021-05-06 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/33959940 A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans. Facial wrinkles (frown lines) 6,254 Latin American individuals NA Illumina [8703729] (imputed) 1 Facial wrinkling http://purl.obolibrary.org/obo/HP_0009762 GCST012108 Genome-wide genotyping array 2021-07-27 33959940 Chen Y 2021-05-06 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/33959940 A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans. Facial wrinkles (crow's feet) 6,254 Latin American individuals NA Illumina [8703729] (imputed) 2 Facial wrinkling http://purl.obolibrary.org/obo/HP_0009762 GCST012107 Genome-wide genotyping array 2021-07-27 33959940 Chen Y 2021-05-06 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/33959940 A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans. Nevus count 6,254 Latin American individuals NA Illumina [8703729] (imputed) 2 nevus count http://www.ebi.ac.uk/efo/EFO_0004632 GCST012106 Genome-wide genotyping array 2021-07-27 33959940 Chen Y 2021-05-06 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/33959940 A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans. Facial wrinkles (principal components analysis) 6,254 Latin American individuals NA Illumina [8703729] (imputed) 2 Facial wrinkling http://purl.obolibrary.org/obo/HP_0009762 GCST012105 Genome-wide genotyping array 2021-07-27 33959940 Chen Y 2021-05-06 Br J Dermatol www.ncbi.nlm.nih.gov/pubmed/33959940 A GWAS identifies novel gene associations with facial skin wrinkling and mole count in Latin-Americans. Facial wrinkles (under eye) 6,254 Latin American individuals NA Illumina [8703729] (imputed) 0 Facial wrinkling http://purl.obolibrary.org/obo/HP_0009762 GCST012104 Genome-wide genotyping array 2021-04-27 32961455 Song W 2020-09-15 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/32961455 Genome-wide association analysis of opioid use disorder: A novel approach using clinical data. Opioid use disorder vs exposed controls 1,039 European ancestry cases, 10,744 European ancestry controls NA Illumina [5508534] (imputed) 2 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST011562 Genome-wide genotyping array 2021-04-27 32961455 Song W 2020-09-15 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/32961455 Genome-wide association analysis of opioid use disorder: A novel approach using clinical data. Opioid use disorder 1,039 European ancestry cases, 20,271 European ancestry controls NA Illumina [5508534] (imputed) 1 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST011563 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL10 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090284 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL2 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088369 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL2A1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088370 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL2L1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088684 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL2L10 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089763 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL2L10 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089764 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL2L2 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087371 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL2L2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089682 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL6 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087380 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCL6 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087578 Genome-wide genotyping array 2022-06-07 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BDNF 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST90087740 Genome-wide genotyping array 2022-06-07 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BDNF 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST90087937 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BDP1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090388 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BECN1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086181 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BECN1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087344 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BET1L 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086515 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BGLAP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90086529 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BGLAP 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90089192 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BGN 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087612 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BGN 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088289 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BHMT2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087839 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BICDL1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086576 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BID 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089210 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BIN1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090757 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BIRC2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086204 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOXL2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086715 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOXM1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086210 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOXO3 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086784 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOXRED1 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089989 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FREM2 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089761 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FRK 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086193 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GAT1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090086 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BACH1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086993 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BACH2 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087207 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAD 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089228 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAG3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086220 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAG4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087263 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAG5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087199 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAGE2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089343 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAGE3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089428 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAMBI 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089580 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BAMBI 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090313 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BARD1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087693 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BATF3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090343 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCAM 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088083 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCAN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088400 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCAP29 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086804 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCAR3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087114 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCAR3 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088988 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BCHE 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090070 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BIRC3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088837 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BIRC5 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088405 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BIRC7 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088742 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BLK 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086693 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BLMH 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087847 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BLVRA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086720 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMP1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 bone morphogenetic protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020184 GCST90088332 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMP10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 bone morphogenetic protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020185 GCST90088444 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMP15 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086556 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMP4 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089352 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMP6 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90088500 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMP6 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90090203 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMP7 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 bone morphogenetic protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020187 GCST90088157 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMPER 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088481 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMPR1A 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088785 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMPR1B 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086334 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMPR2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088786 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BMX 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088371 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BNIP3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089629 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BNIP3L 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089865 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BOC 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088664 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BOLA2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090188 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BOLA3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089251 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BPGM 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086906 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BPI 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088584 Genome-wide genotyping array 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. P3 amplitude reduction 4,166 European ancestry individuals NA NR [21426324] (imputed) 0 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012808 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. P3 genetic factor 3,088 European ancestry individuals NA NR [19284812] (imputed) 0 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012809 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Antisaccade tracking error rate 4,469 European ancestry individuals NA NR [21812431] (imputed) 1 antisaccade response measurement http://www.ebi.ac.uk/efo/EFO_0006874 GCST90012810 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Skin conductance level 3,791 European ancestry individuals NA NR [21085834] (imputed) 0 electrodermal activity measurement http://www.ebi.ac.uk/efo/EFO_0006866 GCST90012811 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Electrodermal activity factor 4,424 European ancestry individuals NA NR [21774103] (imputed) 0 electrodermal activity measurement http://www.ebi.ac.uk/efo/EFO_0006866 GCST90012812 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Overall startle response 3,323 European ancestry individuals NA NR [19722535] (imputed) 1 acoustic startle blink response measurement http://www.ebi.ac.uk/efo/EFO_0006875 GCST90012813 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Aversive difference startle modulation 3,321 European ancestry individuals NA NR [19719458] (imputed) 2 acoustic startle blink response measurement http://www.ebi.ac.uk/efo/EFO_0006875 GCST90012814 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Pleasant difference startle modulation 3,322 European ancestry individuals NA NR [19720993] (imputed) 1 acoustic startle blink response measurement http://www.ebi.ac.uk/efo/EFO_0006875 GCST90012815 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Skin conductance response frequency 4,299 European ancestry individuals NA NR [21572833] (imputed) 0 electrodermal activity measurement http://www.ebi.ac.uk/efo/EFO_0006866 GCST90012816 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Skin conductance response amplitude 4,102 European ancestry individuals NA NR [21289320] (imputed) 1 electrodermal activity measurement http://www.ebi.ac.uk/efo/EFO_0006866 GCST90012817 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Alpha electroencephalogram power 3,948 European ancestry individuals NA NR [20980108] (imputed) 0 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012818 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Beta electroencephalogram power 3,948 European ancestry individuals NA NR [20980108] (imputed) 3 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012819 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Theta electroencephalogram power 3,948 European ancestry individuals NA NR [20980108] (imputed) 1 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012820 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Delta electroencephalogram power 3,948 European ancestry individuals NA NR [20980108] (imputed) 0 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012821 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Total electroencephalogram power 3,948 European ancestry individuals NA NR [20980108] (imputed) 0 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012822 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Alpha electroencephalogram power O1O2 3,966 European ancestry individuals NA NR [21032956] (imputed) 0 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012823 Genome-wide genotyping array, Genome-wide sequencing 2020-12-15 25387710 Vrieze SI 2014-12-01 Psychophysiology www.ncbi.nlm.nih.gov/pubmed/25387710 In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. Alpha electroencephalogram frequency O1O2 3,966 European ancestry individuals NA NR [21032956] (imputed) 2 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST90012824 Genome-wide genotyping array, Genome-wide sequencing 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BPIFA1 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089452 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BPIFA2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089153 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BPIFB1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086636 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BPTF 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087016 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRAT1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086480 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRD1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086819 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRD2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086217 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRD4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086201 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRDT 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087202 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRF1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089026 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRICD5 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089529 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRPF1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086849 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BRSK2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090825 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BSG 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088443 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BST1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088724 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BST2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090327 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTC 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087365 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTC 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090575 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTD 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090597 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTG2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086686 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088373 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTN2A1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090350 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTN3A1 5,320 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089648 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTNL3 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086472 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTNL8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090457 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BTNL9 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089943 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein BUB1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086909 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C10orf10 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089709 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C10orf105 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086619 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C10orf35 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090058 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C10orf54 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086778 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C10orf54 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087801 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C11orf68 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090118 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C11orf87 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086547 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C11orf87 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086883 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C11orf94 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090171 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C12orf10 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090114 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C12orf49 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090676 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C14orf180 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087457 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C14orf93 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089425 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C15orf48 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089403 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C16orf54 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086954 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C17orf67 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090487 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C17orf78 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089503 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C17orf78 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090227 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C18orf32 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090068 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C19orf18 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090694 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1D 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089856 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1GALT1C1 5,314 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089180 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf115 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090157 Genome-wide genotyping array 2021-09-08 33768542 Liu Y 2021-03-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33768542 Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 2,168 European ancestry individuals NA Illumina [NR] (imputed) 1 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST012344 Genome-wide genotyping array 2021-09-08 33768542 Liu Y 2021-03-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33768542 Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 310 African ancestry individuals NA Illumina [NR] (imputed) 10 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST012343 Genome-wide genotyping array 2021-09-08 33768542 Liu Y 2021-03-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33768542 Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 798 Native American individuals NA Illumina [NR] (imputed) 7 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST012342 Genome-wide genotyping array 2021-09-08 33768542 Liu Y 2021-03-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33768542 Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 310 African ancestry individuals, 798 Native American individuals, 112 Asian ancestry individuals, 387 individuals NA Illumina [NR] (imputed) 7 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST012341 Genome-wide genotyping array 2021-09-08 33768542 Liu Y 2021-03-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33768542 Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 2,290 European ancestry individuals, 310 African ancestry individuals, 798 Native American individuals, 112 Asian ancestry individuals, 387 individuals NA Affymetrix, Illumina [NR] (imputed) 1 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST012345 Genome-wide genotyping array 2021-09-08 33768542 Liu Y 2021-03-26 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33768542 Class II HLA Variants Associate with Risk of Pegaspargase Hypersensitivity. Asparaginase hypersensitivity in acute lymphoblastic leukemia 310 African ancestry individuals, 798 Native American individuals, 387 individuals NA Illumina [NR] (imputed) 9 asparaginase hypersensitivity http://www.ebi.ac.uk/efo/EFO_0004881 GCST012340 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB118 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090619 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB119 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086404 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB119 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087452 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB119 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090123 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB119 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090161 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB121 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089207 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB123 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090657 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB124 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089367 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB125 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090713 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB128 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089364 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB129 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090143 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB131 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089579 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB132 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090454 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB134 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086365 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB135 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089408 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB136 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090635 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB4A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087419 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DERL1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087418 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DES 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 C3a anaphylatoxin des arginine measurement http://www.ebi.ac.uk/efo/EFO_0020206 GCST90086908 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DGCR14 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086703 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DGCR2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090017 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DGCR6 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090693 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DGKB 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087297 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DHFR 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090839 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DHH 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088674 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DAG1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090160 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DAPK1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087680 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DAPK2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088670 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DAPP1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086822 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DARS 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087143 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DARS2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086955 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DBNL 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088839 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DBNL 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090802 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCAF5 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086661 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCBLD1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090685 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCBLD2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090639 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCK 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090848 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCLK3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089861 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCN 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088010 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCP1A 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087713 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCP1B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087180 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCTN2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089229 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCTPP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088660 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCUN1D3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087523 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DCUN1D5 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090278 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDC 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088438 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDR1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086873 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDR1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087912 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDR1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088580 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDR2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088454 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAGEA3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087080 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAGEA4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086296 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAGEB10 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086755 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAGI2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087754 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAMDC2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089288 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAN1A1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086668 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAN1A2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090492 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAN1B1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089644 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAN1C1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087434 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAN2B2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090583 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MANBA 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089383 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MANEA 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089986 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MANF 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090563 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MANSC1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090750 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MANSC4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090760 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP1LC3B 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086820 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP2K1 5,327 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088112 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP2K2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088467 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP2K3 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089291 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP2K4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088972 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP3K3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087332 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP4K1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090405 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAP4K3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090423 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088232 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK11 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088862 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DHPS 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090867 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DHX38 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087581 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DHX58 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087716 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DHX8 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086816 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DHX9 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086322 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DIABLO 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 diablo homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020323 GCST90088233 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DIDO1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087867 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DIMT1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087160 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DIRAS3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086962 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DIXDC1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087445 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DKK1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90088437 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GJA1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090922 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GJA8 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087176 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GJD2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086852 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GKN2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089413 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLB1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086338 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLCE 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089847 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLIPR1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090594 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLO1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090884 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLP1R 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087364 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLRX2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087019 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLT8D1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090406 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLTP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087037 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GLTPD2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089942 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GMEB2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087239 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK12 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088863 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK13 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088864 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK14 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088865 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK3 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90088107 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088533 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK9 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088973 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPK9 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090807 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPKAPK2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088529 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPKAPK3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088531 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPKAPK5 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088530 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPKAPK5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090170 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPRE1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087007 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAPT 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089223 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MARCO 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090441 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MARK3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090795 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MASP1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088453 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MASP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090044 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MASP1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090524 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MATK 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088532 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MATN2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088317 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYR61 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089329 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYTH2 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087052 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYTH4 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087200 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYTIP 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087560 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYTL1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090186 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTF 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087919 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTF 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088067 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LUM 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087383 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LY6G6C 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089323 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LY6G6D 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089448 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LY86 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088464 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LY9 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088316 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LY96;TLR4 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088479 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYG1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090576 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase lyn measurement http://www.ebi.ac.uk/efo/EFO_0020827 GCST90088353 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase lyn measurement http://www.ebi.ac.uk/efo/EFO_0020827 GCST90088397 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYPD1 5,324 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090632 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYPD3 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087378 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYPD3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090620 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYPLAL1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086976 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYSMD3 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086344 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYSMD4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090511 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYVE1 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088269 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYZ 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088815 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LYZL2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089379 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein M6PR 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086299 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MACROD1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087585 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAD1L1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087564 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MADCAM1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086642 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAGEA10 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087559 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPC2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088309 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPC3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088783 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPC5 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088851 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPC6 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089012 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPCPD1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087226 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPD1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086531 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPD1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087617 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPD1L 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086969 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPHA2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089395 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPHB5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089354 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPI 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088647 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPIHBP1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087306 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPLD1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086890 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPLD1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090721 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPNMB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088906 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPNMB 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090071 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPNMB 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090106 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPNMB 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090237 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR101 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086713 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR101 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086848 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR107 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087323 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR135 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086761 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR142 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087214 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR26 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087514 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR6 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087881 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDR2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089900 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDX19B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089042 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDX23 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087675 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDX25 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087698 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDX39B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090792 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDX46 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087837 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDX58 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086946 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DDX6 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087280 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEAF1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089373 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DECR1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087153 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEF6 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087774 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFA1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090582 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFA5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089388 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089538 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB103B 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089142 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB104A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089205 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB105B 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086517 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB106A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089133 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB107A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089397 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB108B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089091 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB110 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090139 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB112 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089147 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB113 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087407 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB115 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090178 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DEFB116 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086566 Genome-wide genotyping array 2021-04-13 33662382 Rogne T 2021-03-01 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/33662382 Genome-Wide Association Study Identifies LINC01184/SLC12A2 As Risk Locus for Skin and Soft Tissue Infections. Skin and soft tissue infections 6,107 European ancestry cases and 399,239 European ancestry controls 1,657 European ancestry cases and 67,522 European ancestry controls Affymetrix, Illumina [9211777] (imputed) 5 skin and soft tissue Staphylococcus aureus infection http://www.ebi.ac.uk/efo/EFO_1001489 GCST90013411 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAX1BP1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087185 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAX1BP3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087026 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBC1D5 5,322 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090936 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBCA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087029 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBCE 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086612 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBK1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 serine/threonine-protein kinase TBK1 measurement http://www.ebi.ac.uk/efo/EFO_0020734 GCST90088364 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBL2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086623 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBP 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90088118 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBX22 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086568 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBX3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087694 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBX5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086606 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TBXAS1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090050 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TCEA2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087468 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TCN1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086628 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TCN2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089075 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TCP11 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090135 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TCTA 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086297 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TCTN2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086743 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TDGF1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089214 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TDO2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090883 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TDP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086216 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TEAD3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087271 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TEAD4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087040 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TEC 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 tyrosine-protein kinase TEC measurement http://www.ebi.ac.uk/efo/EFO_0020830 GCST90088478 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TEK 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088510 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SULT4A1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090150 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUMF1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089585 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUMF2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089273 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUMO2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090529 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUMO3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087888 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUN3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090340 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUN5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086644 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SURF1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089983 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUSD1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090764 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUSD2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086187 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUSD3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089196 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SV2A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087288 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SVEP1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086544 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SVEP1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086591 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SWAP70 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087522 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYK 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086423 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086717 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYN3 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089730 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYNCRIP 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088631 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYNE2 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090824 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYNGR3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087408 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT11 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089653 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT17 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090514 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090759 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT3 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086277 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM52 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086596 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM52B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090819 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM57 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086937 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM59L 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090935 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM70 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090033 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM87B 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087471 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM8B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087198 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM9 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090235 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM9 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090581 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMIE 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089969 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMOD1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087092 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMOD2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087270 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMOD3 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087276 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMPO 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090092 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMPRSS11A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089751 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMPRSS11B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086490 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMPRSS11D 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089489 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMPRSS15 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088256 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMPRSS5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089976 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMPRSS6 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086630 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMUB2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090565 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMX2 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086402 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMX3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089125 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNC 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088611 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNF 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90089150 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIGAR 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087011 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIGIT 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090781 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIMM21 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090478 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIMM50 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089799 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIMP1 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087927 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIMP2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087930 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIMP3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087949 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIMP4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089442 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TINAGL1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086599 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TINF2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086383 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIRAP 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090851 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TJP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086900 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TK1 5,322 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088656 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TKT 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088658 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TLL1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089384 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TLN2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087767 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TLR1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086570 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TLR2 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088538 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TLR4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086537 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMCC3 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086670 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMCC3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090383 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMCO5A 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089559 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMED10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089465 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMED2 5,323 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086442 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMED4 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090628 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFB1I1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090291 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFB2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088612 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFB3 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088433 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFBI 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088288 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFBR2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088949 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFBR3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088183 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGIF2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090859 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGM1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086632 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGM3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088703 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THBS1 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088407 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THBS2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087793 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THBS2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088324 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THBS3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090426 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THBS4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088325 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THOC1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090879 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THPO 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089245 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THPO 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090019 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THRA 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087046 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THSD1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089099 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THSD7A 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086588 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THSD7A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090773 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THTPA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087550 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein THYN1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086972 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIAM1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087731 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TIE1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088101 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNF 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90089243 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFAIP3 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087714 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFAIP6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088890 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFAIP8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087071 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF10A 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088780 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF10B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086481 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF10B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089071 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF10B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089783 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF10B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090225 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF10D 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087799 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF11A 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089032 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF11A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090083 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF11A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090124 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF11B 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087958 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF11B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090115 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF12A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088951 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF13B 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088026 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF13C 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089025 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF14 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086290 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF14 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086788 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF14 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089014 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF17 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088009 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF18 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086874 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF18 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089069 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF19 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088947 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TENM2 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086582 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TENM3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086542 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TENM4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086709 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TEPSIN 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089941 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TERF1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086207 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TESC 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087256 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TEX29 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086339 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TEX29 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087485 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TF 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088617 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFAM 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090930 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFF1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090541 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFF2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086291 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFF2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090546 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFF3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088766 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFF3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090128 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFIP11 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090467 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFPI 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088323 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFPI2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090570 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFR2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086781 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFRC 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089553 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TFRC 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090303 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TG 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088619 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090653 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFB1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087790 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TGFB1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087933 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT5 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090508 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT7 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089671 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT8 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089933 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYT9 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090025 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYTL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087294 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYTL4 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086799 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SYTL4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090502 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAB1;MAP3K7 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088985 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAC1 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086308 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAC1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090638 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAC3 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089873 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAC4 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089447 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TACO1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090588 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TACSTD2 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087730 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TACSTD2 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087985 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAGLN 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090803 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAGLN2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086830 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAGLN2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090550 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TALDO1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086695 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TANK 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087717 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAPBP 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086944 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TAPBPL 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089368 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TARBP2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087222 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TARDBP 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086912 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TARP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090716 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM105 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086449 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM106A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086305 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM106B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090262 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM108 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086354 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM119 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086545 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM132A 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089891 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM132B 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090363 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM132C 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086555 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM132C 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089706 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM132D 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087429 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM154 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086621 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM167A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086546 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM167B 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087430 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM185A 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087892 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM190 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086271 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090433 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM230 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086785 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM234 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090056 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM237 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087273 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM25 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090448 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM27 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087309 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM27 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089853 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM38B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090727 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM40 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087316 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TMEM41B 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086393 Genome-wide genotyping array 2021-10-13 29878111 Kocarnik JM 2018-08-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29878111 Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study. C-reactive protein levels 15,895 Hispanic individuals, 12,817 African American individuals, 1,252 Asian or Oceanian ancestry individuals, 539 Native American ancestry individuals NA Illumina [~ 200000] 18 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST012480 Targeted genotyping array [Metabochip] 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Bilirubin (z,z) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90026002 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cholesterol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90026003 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Lysine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90026004 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Tyrosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90026005 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Pyroglutamine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST90026006 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cortisol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90026007 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Lactate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90026008 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90026009 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1,5-anhydroglucitol (1,5-ag) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90026010 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Kynurenine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90026011 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Asparagine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90026012 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glycine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90026013 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Proline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90026014 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ornithine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90026015 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Citrulline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90026016 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Acetoacetate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90026017 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026018 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026019 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026020 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026021 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026022 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026023 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026024 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90026025 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Allantoin levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90026026 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Alpha-ketoglutarate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90026027 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Dimethylglycine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90026028 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glucuronate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90026029 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glycerol 3-phosphate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90026030 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Hypoxanthine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90026031 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-indoxyl sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010502 GCST90026032 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Inosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90026033 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Malate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90026034 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Taurine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90026035 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Uridine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90026036 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Xanthine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90026037 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Phosphate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90026038 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxyisobutyrate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90026039 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5-oxoproline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90026040 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. P-cresol sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90026041 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. (N(1) + N(8))-acetylspermidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026042 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1,2-dipalmitoyl-gpc (16:0/16:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026043 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026044 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-(1-enyl-palmitoyl)-2-oleoyl-gpc (p-16:0/18:1) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026045 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-arachidonoyl-gpc (20:4n6) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026046 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-linoleoyl-gpc (18:2) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026047 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-methylhistidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026048 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-methylnicotinamide levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026049 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-myristoyl-2-palmitoyl-gpc (14:0/16:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026050 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-oleoyl-GPC (18:1) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026051 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23308 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026315 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ethyl beta-glucopyranoside levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026316 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23587 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026317 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23590 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026318 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23593 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026319 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23639 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026320 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23644 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026321 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23652 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026322 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-23739 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026323 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24228 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026324 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24295 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026325 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-(3-amino-3-carboxypropyl)uridine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026326 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24337 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026327 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24431 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026328 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24452 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026329 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24686 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026330 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24699 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026331 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-amino-2-piperidone levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026332 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24813 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026333 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-24952 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026334 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-25109 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026335 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N6-methyllysine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026336 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glucose levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90025999 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Creatinine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90026000 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Urate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90026001 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026052 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-palmitoyl-2-docosahexaenoyl-gpc (16:0/22:6) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026053 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-palmitoyl-2-linoleoyl-gpc (16:0/18:2) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026054 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-palmitoyl-2-oleoyl-gpc (16:0/18:1) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026055 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026056 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026057 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026058 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-ribosyl-imidazoleacetate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026059 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026060 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-stearoyl-2-docosahexaenoyl-gpc (18:0/22:6) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026061 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-stearoyl-2-linoleoyl-gpc (18:0/18:2) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026062 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-stearoyl-2-oleoyl-gpc (18:0/18:1) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026063 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-stearoyl-gpc (18:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026064 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2'-deoxyuridine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026065 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2'-o-methylcytidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026066 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2,3-dihydroxy-2-methylbutyrate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026067 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2,3-dihydroxyisovalerate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026068 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-aminobutyrate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026069 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-aminophenol sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026070 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-hydroxy-3-methylvalerate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026071 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-hydroxyadipate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026072 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-hydroxybutyrate/2-hydroxyisobutyrate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026073 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-hydroxyglutarate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026074 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-oxoadipate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026075 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-piperidinone levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026076 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma alpha aminoadipic acid levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 0 aminoadipic acid measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0010459, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102475 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma arginine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 0 arginine measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0020990, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102474 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma ethanolamine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 1 ethanolamine measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0020991, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102476 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma histidine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 0 histidine measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0009769, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102477 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma threonine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 0 response to acamprosate, threonine measurement http://www.ebi.ac.uk/efo/EFO_0020993, http://www.ebi.ac.uk/efo/EFO_0009775 GCST90102478 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma hydroxyproline levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 0 hydroxyproline measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0010498, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102479 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma alpha-amino-N-butyric acid levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 1 alpha-amino-N-butyric acid measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0020992, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102480 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma asparagine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 1 asparagine measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0009766, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102481 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma lysine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 1 lysine measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0005002, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102482 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma taurine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 1 taurine measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0010536, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102483 Genome-wide genotyping array 2022-05-26 35016259 Ho MF 2022-01-11 Br J Pharmacol www.ncbi.nlm.nih.gov/pubmed/35016259 Genetic Variants Associated with Acamprosate Treatment Response in Alcohol Use Disorder Patients: A Multiple Omics Study. Plasma tyrosine levels in alcohol use disorder treated with acamprosate 442 individuals NA Illumina [6621773] (imputed) 1 tyrosine measurement, response to acamprosate http://www.ebi.ac.uk/efo/EFO_0005058, http://www.ebi.ac.uk/efo/EFO_0020993 GCST90102484 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-11795 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026290 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-12007 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026291 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-12015 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026292 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-12100 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026293 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-12101 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026294 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-12104 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026295 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ascorbic acid 3-sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026296 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-12411 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026297 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-12906 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026298 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-carboxyethylvaline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026299 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-13728 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026300 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-14056 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026301 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-methyl-5-imidazoleacetate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026302 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-15245 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026303 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 1-carboxyethylphenylalanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026304 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-15674 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026305 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N,n,n-trimethyl-alanylproline betaine (tmap) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026306 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-18887 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026307 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-19438 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026308 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-21286 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026309 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Butyrate (4:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026310 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-21733 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026311 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2-o-methylascorbic acid levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026312 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-22162 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026313 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 4-chlorobenzoic acid levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026314 Genome-wide genotyping array 2021-08-26 33745150 de Coo A 2021-03-21 J Clin Periodontol www.ncbi.nlm.nih.gov/pubmed/33745150 Genome-wide association study of stage III/IV grade C periodontitis (former aggressive periodontitis) in a Spanish population. Periodontitis (stage III/IV grade C) 465 Spanish ancestry cases, 1,179 Spanish ancestry controls NA Affymetrix [645639] (imputed) 8 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST012245 Genome-wide genotyping array 2021-07-02 33385400 Patrick MT 2020-12-29 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/33385400 Causal relationship and shared genetic loci between psoriasis and type 2 diabetes through trans-disease meta-analysis. Psoriasis or type 2 diabetes (trans-disease meta-analysis) 11,024 European ancestry psoriasis cases, 74,124 European ancestry diabetes cases, 840,342 European ancestry controls NA NR [8016731] (imputed) 43 psoriasis, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000676, http://purl.obolibrary.org/obo/MONDO_0005148 GCST011991 Genome-wide genotyping array 2021-07-02 33385400 Patrick MT 2020-12-29 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/33385400 Causal relationship and shared genetic loci between psoriasis and type 2 diabetes through trans-disease meta-analysis. Psoriasis or type 2 diabetes (trans-disease meta-analysis)(opposite effect) 11,024 European ancestry psoriasis cases, 74,124 European ancestry diabetes cases, 840,342 European ancestry controls NA NR [8016731] (imputed) 32 psoriasis, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000676, http://purl.obolibrary.org/obo/MONDO_0005148 GCST011990 Genome-wide genotyping array 2022-05-27 35122707 Jiang M 2022-02-05 J Eur Acad Dermatol Venereol www.ncbi.nlm.nih.gov/pubmed/35122707 Unique motif shared by HLA-B*59:01 and HLA-B*55:02 is associated with methazolamide-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in Han Chinese. Methazolamide-induced Stevens-Johnson syndrome / toxic epidermal necrolysis 15 Han Chinese ancestry cases, 806 Han Chinese ancestry controls NA Illumina [151355] 12 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to methazolamide http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://www.ebi.ac.uk/efo/EFO_0020996 GCST90103749 Exome-wide sequencing 2021-09-01 33782385 Andlauer TFM 2021-03-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33782385 Genetic factors influencing a neurobiological substrate for psychiatric disorders. Common neurobiological substrate measurement (PC1) 2,271 individuals 865 individuals Affymetrix, Illumina [up to 8620154] (imputed) 1 grey matter volume measurement http://www.ebi.ac.uk/efo/EFO_0005420 GCST012278 Genome-wide genotyping array 2022-01-05 33782385 Andlauer TFM 2021-03-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33782385 Genetic factors influencing a neurobiological substrate for psychiatric disorders. Common neurobiological substrate measurement (PC1) 3,136 individuals NA Affymetrix, Illumina [up to 8620154] (imputed) 0 grey matter volume measurement http://www.ebi.ac.uk/efo/EFO_0005420 GCST012617 Genome-wide genotyping array 2021-06-04 33359885 Gettler K 2020-12-24 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/33359885 Common and rare variant prediction and penetrance of IBD in a large, multi-ethnic, health system-based biobank cohort. Inflammatory bowel disease 15,507 European ancestry cases, 25,403 European ancestry controls, 2,345 African American cases, 5,002 African American controls NA NR [18368734] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST011786 Genome-wide genotyping array 2021-09-07 34216518 Osman Y 2021-07-03 Int J Lab Hematol www.ncbi.nlm.nih.gov/pubmed/34216518 Functional multigenic variations associated with hodgkin lymphoma. Hodgkin's lymphoma 56 Greater Middle Eastern ancestry cases, 5 unknown ancestry cases, 36 Greater Middle Eastern ancestry controls NA Illumina [243345] 35 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST012335 Exome genotyping array [Exome array] 2022-10-26 34619205 Zhong R 2021-10-05 Sci Total Environ www.ncbi.nlm.nih.gov/pubmed/34619205 Genome-wide gene-bisphenol A, F and triclosan interaction analyses on urinary oxidative stress markers. 8-isoprostaglandin-F2alpha x bisphenol A interaction 416 Chinese ancestry individuals NA Illumina [4592041] (imputed) 1 8-isoprostaglandin-F2alpha measurement, bisphenol A measurement http://www.ebi.ac.uk/efo/EFO_0801082, http://www.ebi.ac.uk/efo/EFO_0801079 GCST90061013 Genome-wide genotyping array 2022-10-26 34619205 Zhong R 2021-10-05 Sci Total Environ www.ncbi.nlm.nih.gov/pubmed/34619205 Genome-wide gene-bisphenol A, F and triclosan interaction analyses on urinary oxidative stress markers. 8-isoprostaglandin-F2alpha x triclosan interaction 416 Chinese ancestry individuals NA Illumina [4592041] (imputed) 1 triclosan measurement, 8-isoprostaglandin-F2alpha measurement http://www.ebi.ac.uk/efo/EFO_0801078, http://www.ebi.ac.uk/efo/EFO_0801082 GCST90061014 Genome-wide genotyping array 2022-10-26 34619205 Zhong R 2021-10-05 Sci Total Environ www.ncbi.nlm.nih.gov/pubmed/34619205 Genome-wide gene-bisphenol A, F and triclosan interaction analyses on urinary oxidative stress markers. 8-hydroxydeoxyguanosine x triclosan interaction 416 Chinese ancestry individuals NA Illumina [4592041] (imputed) 3 triclosan measurement, 8-hydroxydeoxyguanosine measurement http://www.ebi.ac.uk/efo/EFO_0801078, http://www.ebi.ac.uk/efo/EFO_0801081 GCST90061015 Genome-wide genotyping array 2021-11-26 34384552 Ghouse J 2021-08-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/34384552 Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors. Angioedema in response to angiotensin-converting enzyme inhibitor 462 European ancestry ACE inhibitor-associated angioedema cases, 53,391 European ancestry ACE inhibitor-exposed controls 142 European ancestry ACE inhibitor-associated angioedema cases, 1,345 European ancestry ACE inhibitor-exposed controls Illumina [NR] (imputed) 1 response to angiotensin-converting enzyme inhibitor, angioedema http://www.ebi.ac.uk/efo/EFO_0005325, http://www.ebi.ac.uk/efo/EFO_0005532 GCST90027157 Genome-wide genotyping array 2021-04-21 32920024 Sanna M 2020-09-10 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/32920024 Looking for Sunshine: Genetic Predisposition to Sun-Seeking in 265,000 Individuals of European Ancestry. Sun-seeking behavior 261,915 European ancestry individuals NA Affymetrix, Illumina [8385325] (imputed) 5 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST011534 Genome-wide genotyping array 2022-10-25 34584012 Tietz AK 2021-09-28 Neurol Neuroimmunol Neuroinflamm www.ncbi.nlm.nih.gov/pubmed/34584012 Genome-wide Association Study Identifies 2 New Loci Associated With Anti-NMDAR Encephalitis. Anti-N-methyl-D-aspartate receptor encephalitis 178 European ancestry cases, 590 European ancestry controls NA Illumina [8073349] (imputed) 2 GCST90058029 Genome-wide genotyping array 2022-05-19 35126453 Zhou Y 2022-01-20 Front Genet www.ncbi.nlm.nih.gov/pubmed/35126453 Shared Genetic Architecture and Causal Relationship Between Asthma and Cardiovascular Diseases: A Large-Scale Cross-Trait Analysis. Asthma and cardiovascular disease 19,954 European ancestry cases, 107,715 European ancestry controls NA NR [NR] 145 asthma, cardiovascular disease http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0000319 GCST90103427 Genome-wide genotyping array 2022-10-27 36142332 Hsu LA 2022-09-08 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/36142332 Common and Rare PCSK9 Variants Associated with Low-Density Lipoprotein Cholesterol Levels and the Risk of Diabetes Mellitus: A Mendelian Randomization Study. LDL cholesterol levels 75,441 East Asian ancestry individuals NA Affymetrix [3639888] (imputed) 47 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90179477 Genome-wide genotyping array 2021-04-27 33766035 Wakim V 2021-03-25 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33766035 New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population. Severe coronary stenosis (family history of CAD interaction) 1,734 Middle Eastern ancestry cases, 757 Middle Eastern ancestry controls NA Illumina [NR] 1 family history, coronary stenosis, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0000493, http://purl.obolibrary.org/obo/MONDO_0006715, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011565 Genome-wide genotyping array 2021-04-27 33766035 Wakim V 2021-03-25 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33766035 New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population. Severe coronary stenosis (young age of onset interaction) 1,734 Middle Eastern ancestry cases, 757 Middle Eastern ancestry controls NA Illumina [NR] 4 age at onset, coronary stenosis http://www.ebi.ac.uk/efo/EFO_0004847, http://purl.obolibrary.org/obo/MONDO_0006715 GCST011564 Genome-wide genotyping array 2021-04-27 33766035 Wakim V 2021-03-25 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33766035 New susceptibility alleles associated with severe coronary artery stenosis in the Lebanese population. Severe coronary stenosis 1,734 Middle Eastern ancestry cases, 757 Middle Eastern ancestry controls NA Illumina [NR] 2 coronary stenosis http://purl.obolibrary.org/obo/MONDO_0006715 GCST011566 Genome-wide genotyping array 2021-09-07 34380431 Tsai CK 2021-08-11 J Headache Pain www.ncbi.nlm.nih.gov/pubmed/34380431 Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. Migraine age at onset (before 12 years vs after 12 years) 715 Han Chinese ancestry individuals NA Affymetrix [NR] 1 age of onset of migraine disorder http://purl.obolibrary.org/obo/OBA_2001026 GCST90027230 Genome-wide genotyping array 2021-09-07 34380431 Tsai CK 2021-08-11 J Headache Pain www.ncbi.nlm.nih.gov/pubmed/34380431 Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. Migraine age at onset before 12 years (aura vs without aura) 715 Han Chinese ancestry individuals NA Affymetrix [NR] 0 age of onset of migraine disorder http://purl.obolibrary.org/obo/OBA_2001026 GCST90027231 Genome-wide genotyping array 2021-09-07 34380431 Tsai CK 2021-08-11 J Headache Pain www.ncbi.nlm.nih.gov/pubmed/34380431 Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. Migraine age at onset after 12 years (aura vs without aura) 715 Han Chinese ancestry individuals NA Affymetrix [NR] 0 age of onset of migraine disorder http://purl.obolibrary.org/obo/OBA_2001026 GCST90027232 Genome-wide genotyping array 2021-09-07 34380431 Tsai CK 2021-08-11 J Headache Pain www.ncbi.nlm.nih.gov/pubmed/34380431 Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. Migraine (age at onset) 715 Han Chinese ancestry individuals NA Affymetrix [NR] 1 age of onset of migraine disorder http://purl.obolibrary.org/obo/OBA_2001026 GCST90027233 Genome-wide genotyping array 2021-09-07 34380431 Tsai CK 2021-08-11 J Headache Pain www.ncbi.nlm.nih.gov/pubmed/34380431 Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. Migraine with aura (age at onset) 167 Han Chinese ancestry individuals NA Affymetrix [NR] 4 age of onset of migraine with aura http://purl.obolibrary.org/obo/OBA_2001027 GCST90027234 Genome-wide genotyping array 2021-09-07 34380431 Tsai CK 2021-08-11 J Headache Pain www.ncbi.nlm.nih.gov/pubmed/34380431 Identifying genetic variants for age of migraine onset in a Han Chinese population in Taiwan. Migraine without aura (age at onset) 548 Han Chinese ancestry individuals NA Affymetrix [NR] 1 age of onset of migraine without aura http://purl.obolibrary.org/obo/OBA_2001028 GCST90027235 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Barnesiella.s_Barnesiella_intestinihominis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027763 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Coprobacter.s_Coprobacter_fastidiosus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027764 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Odoribacter.s_Odoribacter_splanchnicus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027765 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Parabacteroides.s_Parabacteroides_distasonis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027766 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Parabacteroides.s_Parabacteroides_goldsteinii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027767 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Parabacteroides.s_Parabacteroides_johnsonii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027768 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_finegoldii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027827 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_fragilis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027828 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_intestinalis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027829 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_massiliensis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027830 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_nordii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027831 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_ovatus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027832 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_plebeius) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027833 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_salyersiae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027834 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_stercoris) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027835 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_thetaiotaomicron) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027836 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_uniformis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027837 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_vulgatus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027838 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_xylanisolvens) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027839 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Blautia.s_Ruminococcus_obeum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027840 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Blautia.s_Ruminococcus_torques) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027841 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Butyrivibrio.s_Butyrivibrio_crossotus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027842 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Coprococcus.s_Coprococcus_catus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027843 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Coprococcus.s_Coprococcus_comes) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027844 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Coprococcus.s_Coprococcus_sp_ART55_1) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027845 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. Low density lipoprotein cholesterol levels 10,389 Sub-Saharan African ancestry individuals NA Illumina [13900000] (imputed) 7 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90101741 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. High density lipoprotein cholesterol levels 10,488 Sub-Saharan African ancestry individuals NA Illumina [13900000] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90101742 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. Total cholesterol levels 10,486 Sub-Saharan African ancestry individuals NA Illumina [13900000] (imputed) 4 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90101743 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. Triglyceride levels 10,474 Sub-Saharan African ancestry individuals NA Illumina [13900000] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90101744 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. Low density lipoprotein cholesterol levels 24,515 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [22000000] (imputed) 11 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90101745 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. High density lipoprotein cholesterol levels 24,616 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [22000000] (imputed) 7 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90101746 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. Total cholesterol levels 24,612 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [22000000] (imputed) 9 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90101747 Genome-wide genotyping array 2022-05-24 35546142 Choudhury A 2022-05-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35546142 Meta-analysis of sub-Saharan African studies provides insights into genetic architecture of lipid traits. Triglyceride levels 24,600 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [22000000] (imputed) 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90101748 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Dorea.s_Dorea_formicigenerans) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027846 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Dorea.s_Dorea_longicatena) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027847 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Dorea.s_Dorea_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027848 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Lachnospiraceae_noname.s_Lachnospiraceae_bacterium_1_1_57FAA) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027849 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Lachnospiraceae_noname.s_Lachnospiraceae_bacterium_3_1_46FAA) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027850 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Lachnospiraceae_noname.s_Lachnospiraceae_bacterium_5_1_63FAA) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027851 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Lachnospiraceae_noname.s_Lachnospiraceae_bacterium_7_1_58FAA) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027852 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Lachnospiraceae_noname.s_Lachnospiraceae_bacterium_8_1_57FAA) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027853 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Roseburia.s_Roseburia_hominis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027854 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Roseburia.s_Roseburia_intestinalis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027855 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Roseburia.s_Roseburia_inulinivorans) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027856 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Roseburia.s_Roseburia_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027857 Genome-wide genotyping array 2021-10-20 34409643 Freitag-Wolf S 2021-08-18 J Clin Periodontol www.ncbi.nlm.nih.gov/pubmed/34409643 Sex-specific genetic factors affect the risk of early-onset periodontitis in Europeans. Early onset periodontitis x sex interaction 545 Dutch ancestry women, 351 Dutch ancestry men NA Illumina [79780573] (imputed) 4 sex interaction measurement, aggressive periodontitis http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0006342 GCST90027904 Genome-wide genotyping array 2021-11-22 34642315 Ferreiro-Iglesias A 2021-10-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34642315 Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer. Human papilloma virus 16 positive oropharyngeal cancer 1,078 European ancestry cases, 5,256 European ancestry controls NA Illumina [7574753] (imputed) 14 human papilloma virus infection, oropharynx cancer http://www.ebi.ac.uk/efo/EFO_0001668, http://www.ebi.ac.uk/efo/EFO_1001931 GCST90085699 Genome-wide genotyping array 2021-11-22 34642315 Ferreiro-Iglesias A 2021-10-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34642315 Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer. Human papilloma virus 16 negative oropharyngeal cancer 565 European ancestry cases, 5,256 European ancestry controls NA Illumina [7574753] (imputed) 23 human papilloma virus infection, oropharynx cancer http://www.ebi.ac.uk/efo/EFO_0001668, http://www.ebi.ac.uk/efo/EFO_1001931 GCST90085700 Genome-wide genotyping array 2021-11-22 34642315 Ferreiro-Iglesias A 2021-10-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34642315 Germline determinants of humoral immune response to HPV-16 protect against oropharyngeal cancer. Oropharynx cancer and human papilloma virus 16 negative oropharyngeal cancer 2,359 European ancestry cases, 565 European ancestry controls NA Illumina [up to 7574753] (imputed) 28 human papilloma virus infection, oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0001668, http://www.ebi.ac.uk/efo/EFO_0005570 GCST90085701 Genome-wide genotyping array 2021-10-22 34456681 Song M 2021-08-12 Front Neurosci www.ncbi.nlm.nih.gov/pubmed/34456681 Genome-Wide Meta-Analysis Identifies Two Novel Risk Loci for Epilepsy. Epilepsy 19,122 European ancestry cases, 168,998 European ancestry controls, 2,143 Japanese ancestry cases, 210,310 Japanese ancestry controls, 5,087 cases, 395,209 controls NA NR [NR] 3 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90027898 Genome-wide genotyping array 2021-07-27 34255042 Schmitz D 2021-07-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/34255042 Genome-Wide Association Study of Estradiol Levels, and the Causal Effect of Estradiol on Bone Mineral Density. Estradiol levels 13,367 European ancestry male cases, 134,323 European ancestry male controls NA Affymetrix [7871717] (imputed) 14 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90020091 Genome-wide genotyping array 2021-07-27 34255042 Schmitz D 2021-07-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/34255042 Genome-Wide Association Study of Estradiol Levels, and the Causal Effect of Estradiol on Bone Mineral Density. Estradiol levels 37,461 European ancestry female cases, 126,524 European ancestry female controls NA Affymetrix [7871717] (imputed) 2 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90020092 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Cystatin C levels 437,846 European ancestry individuals NA NR [9800000] (imputed) 27 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90025945 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Creatinine levels 437,660 European ancestry individuals NA NR [9800000] (imputed) 23 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90025946 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Serum alkaline phosphatase levels 437,896 European ancestry individuals NA NR [9800000] (imputed) 68 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90025947 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Serum phosphate levels 400,159 European ancestry individuals NA NR [9800000] (imputed) 14 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90025948 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Height 458,235 European ancestry individuals NA NR [9800000] (imputed) 58 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90025949 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Monocyte count 443,529 European ancestry individuals NA NR [9800000] (imputed) 21 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90025950 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Platelet count 444,866 European ancestry individuals NA NR [9800000] (imputed) 46 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90025951 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Apolipoprotein B levels 435,744 European ancestry individuals NA NR [9800000] (imputed) 29 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90025952 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Total cholesterol levels 437,878 European ancestry individuals NA NR [9800000] (imputed) 30 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90025953 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Direct low density lipoprotein cholesterol levels 437,068 European ancestry individuals NA NR [9800000] (imputed) 27 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90025954 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Apolipoprotein A1 levels 398,508 European ancestry individuals NA NR [9800000] (imputed) 59 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90025955 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. HDL cholesterol levels 400,754 European ancestry individuals NA NR [9800000] (imputed) 65 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90025956 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Triglyceride levels 437,532 European ancestry individuals NA NR [9800000] (imputed) 36 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90025957 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Sex hormone-binding globulin levels 397,043 European ancestry individuals NA NR [9800000] (imputed) 22 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90025958 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. C-reactive protein levels 436,939 European ancestry individuals NA NR [9800000] (imputed) 15 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90025959 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Mean platelet volume 445,364 European ancestry individuals NA NR [9800000] (imputed) 55 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90025960 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Platelet distribution width 445,262 European ancestry individuals NA NR [9800000] (imputed) 35 platelet component distribution width http://www.ebi.ac.uk/efo/EFO_0007984 GCST90025961 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Mean corpuscular hemoglobin concentration 443,081 European ancestry individuals NA NR [9800000] (imputed) 24 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90025962 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Mean corpuscular volume 444,035 European ancestry individuals NA NR [9800000] (imputed) 22 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90025963 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Red blood cell count 445,305 European ancestry individuals NA NR [9800000] (imputed) 23 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90025964 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Urate levels 437,354 European ancestry individuals NA NR [9800000] (imputed) 35 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90025965 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Gamma glutamyl transferase levels 437,651 European ancestry individuals NA NR [9800000] (imputed) 24 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90025966 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Vitamin D levels 418,691 European ancestry individuals NA NR [9800000] (imputed) 7 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90025967 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Systolic blood pressure 422,713 European ancestry individuals NA NR [9800000] (imputed) 11 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90025968 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Hemoglobin levels 445,373 European ancestry individuals NA NR [9800000] (imputed) 19 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90025969 Genome-wide genotyping array 2021-12-09 33713768 Akenroye AT 2021-03-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/33713768 Genome-wide Association study of Asthma, Total IgE, and Lung function in a Cohort of Peruvian Children. Asthma (childhood onset) 436 Peruvian cases, 291 Peruvian controls NA Illumina [NR] (imputed) 9 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90091010 Genome-wide genotyping array 2021-12-09 33713768 Akenroye AT 2021-03-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/33713768 Genome-wide Association study of Asthma, Total IgE, and Lung function in a Cohort of Peruvian Children. Serum IgE levels 727 Peruvian individuals NA Illumina [NR] (imputed) 18 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST90091011 Genome-wide genotyping array 2021-12-09 33713768 Akenroye AT 2021-03-10 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/33713768 Genome-wide Association study of Asthma, Total IgE, and Lung function in a Cohort of Peruvian Children. Lung function (FEV1 percent predicted) 727 Peruvian individuals up to 2,583 Hispanic or Latin American individuals Illumina [NR] (imputed) 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90091012 Genome-wide genotyping array 2021-12-09 31903547 Pei YF 2020-01-05 Clin Genet www.ncbi.nlm.nih.gov/pubmed/31903547 Bivariate genome-wide association analysis identified three pleiotropic loci underlying osteoporosis and obesity. Body mass index 14,489 individuals 217,822 individuals NR [6879267] 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090977 Genome-wide genotyping array 2021-12-09 31903547 Pei YF 2020-01-05 Clin Genet www.ncbi.nlm.nih.gov/pubmed/31903547 Bivariate genome-wide association analysis identified three pleiotropic loci underlying osteoporosis and obesity. Body mass index and bone mineral density (pleiotropy) 14,489 individuals 217,822 individuals NR [6879267] 3 bone density, body mass index http://www.ebi.ac.uk/efo/EFO_0003923, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090978 Genome-wide genotyping array 2021-12-09 31903547 Pei YF 2020-01-05 Clin Genet www.ncbi.nlm.nih.gov/pubmed/31903547 Bivariate genome-wide association analysis identified three pleiotropic loci underlying osteoporosis and obesity. Bone mineral density 14,489 individuals 217,822 individuals NR [6879267] 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90090979 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to ibrutinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044881 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to masatinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044882 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to nilotinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044883 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to nintedanib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 1 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044884 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to sorafenib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044885 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to sunitinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044886 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to tivantinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 1 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044887 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to trametinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 7 response to trametinib http://www.ebi.ac.uk/efo/EFO_0007816 GCST90044888 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to vandetanib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 1 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044889 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to vemurafenib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 3 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044890 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to hydroxyurea 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to hydroxyurea http://purl.obolibrary.org/obo/GO_0072710 GCST90044847 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to mitomycin C 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90044848 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to temozolomide 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to temozolomide http://purl.obolibrary.org/obo/GO_1990054 GCST90044849 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to paclitaxel and epirubicin 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to combination chemotherapy http://www.ebi.ac.uk/efo/EFO_0007965 GCST90044850 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to etoposide 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to etoposide http://purl.obolibrary.org/obo/GO_1902521 GCST90044851 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to teniposide 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90044852 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to daunorubicin 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to topoisomerase inhibitor http://purl.obolibrary.org/obo/GO_0072758 GCST90044853 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to doxorubicin 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to doxorubicin http://purl.obolibrary.org/obo/GO_1902520 GCST90044854 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to epirubicin 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to 4'-epidoxorubicin http://purl.obolibrary.org/obo/GO_1902522 GCST90044855 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to mitoxantrone 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to topoisomerase inhibitor http://purl.obolibrary.org/obo/GO_0072758 GCST90044857 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to topotecan 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to topoisomerase inhibitor http://purl.obolibrary.org/obo/GO_0072758 GCST90044858 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to taxane treatment (docetaxel) 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 1 response to docetaxel trihydrate http://purl.obolibrary.org/obo/GO_1902519 GCST90044859 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to paclitaxel 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 methylcobalamin deficiency type cblE http://purl.obolibrary.org/obo/MONDO_0009354 GCST90044860 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to vinblastine 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 1 response to antimicrotubule agent http://www.ebi.ac.uk/efo/EFO_0005260 GCST90044861 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to vincristine sulfate 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to vincristine http://www.ebi.ac.uk/efo/EFO_0006950 GCST90044862 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to vinorelbine 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 1 response to antimicrotubule agent http://www.ebi.ac.uk/efo/EFO_0005260 GCST90044863 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to azacytidine 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90044864 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to cladaribine 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90044865 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to cytosine beta-D-arabinoside 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to cytosine arabinoside http://www.ebi.ac.uk/efo/EFO_0005655 GCST90044866 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to fludarabine 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90044867 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to cytidine analogues (gemcitabine) 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 4 response to gemcitabine http://purl.obolibrary.org/obo/GO_0036272 GCST90044868 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to 5-fluorouracil 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to fluoropyrimidines http://www.ebi.ac.uk/efo/EFO_0010825 GCST90044869 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to fluoro-deoxyuridine 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to fluoropyrimidines http://www.ebi.ac.uk/efo/EFO_0010825 GCST90044870 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to arsenic trioxide 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90044871 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to platinum-based chemotherapy (carboplatin) 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 1 response to carboplatin http://purl.obolibrary.org/obo/GO_0097328 GCST90044872 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to oxaliplatin 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 3 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST90044873 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to apatinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044874 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to axitinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044875 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to cabozantinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044876 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to crizotinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044877 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to dasatinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044878 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to dovitinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 2 response to tyrosine kinase inhibitor http://www.ebi.ac.uk/efo/EFO_0009170 GCST90044879 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to erlotinib 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 9 response to erlotinib http://www.ebi.ac.uk/efo/EFO_0007868 GCST90044880 Genome-wide genotyping array 2022-03-22 34785643 Park JY 2021-11-16 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34785643 A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages. Hippocampal volume 2,643 Korean ancestry individuals NA NR [3930740] (imputed) 4 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90095658 Genome-wide genotyping array 2022-03-22 34785643 Park JY 2021-11-16 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34785643 A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages. Entorhinal cortical thickness 2,643 Korean ancestry individuals NA NR [3930740] (imputed) 4 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90095659 Genome-wide genotyping array 2022-03-22 34785643 Park JY 2021-11-16 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34785643 A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages. Superior frontal cortical thickness 2,643 Korean ancestry individuals NA NR [3930740] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90095660 Genome-wide genotyping array 2022-03-22 34785643 Park JY 2021-11-16 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34785643 A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages. Middle temporal cortical thickness 2,643 Korean ancestry individuals NA NR [3930740] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90095661 Genome-wide genotyping array 2022-03-22 34785643 Park JY 2021-11-16 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34785643 A missense variant in SHARPIN mediates Alzheimer's disease-specific brain damages. Inferior parietal cortical thickness 2,643 Korean ancestry individuals NA NR [3930740] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90095662 Genome-wide genotyping array 2022-01-19 34657909 Takei M 2021-10-16 Biol Pharm Bull www.ncbi.nlm.nih.gov/pubmed/34657909 A genome-wide association study predicts the onset of dysgeusia due to anti-cancer drug treatment. Dysgeusia in anti-cancer drug treatment 48 East Asian ancestry cases, 28 East Asian ancestry controls NA Illumina [659184] 0 Abnormality of taste sensation, response to antineoplastic agent http://purl.obolibrary.org/obo/HP_0000223, http://purl.obolibrary.org/obo/GO_0097327 GCST012657 Genome-wide genotyping array 2021-11-01 34437536 Akhtari FS 2021-08-26 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34437536 High-throughput screening and genome-wide analyses of 44 anticancer drugs in the 1000 Genomes cell lines reveals an association of the NQO1 gene with the response of multiple anticancer drugs. Response to idarubicin 680 lymphoblastoid cell lines from Han Chinese ancestry, Japanese ancestry, Kenyan ancestry, Mexican ancestry, Tuscan ancestry, Yoruban ancestry, British ancestry, Columbian ancestry individuals NA Illumina [1510701] 0 response to topoisomerase inhibitor http://purl.obolibrary.org/obo/GO_0072758 GCST90044856 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90026495 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (basophil) 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90026496 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (eosinophil) 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90026497 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (lymphocyte) 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90026498 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (monocyte) 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90026499 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (neutrophil) 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90026500 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Platelet count 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90026501 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Mean platelet volume 16,201 African American or Afro-Caribbean individuals, 21,347 Hispanic or Latin American individuals, 27,236 European ancestry individuals 728,194 European ancestry, East Asian ancestry, African American or Afro-Caribbean, Hispanic or Latin American, South Asian ancestry individuals Affymetrix, Illumina [39723562] (imputed) 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90026502 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 86 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90026503 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (basophil) 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 1 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90026504 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (eosinophil) 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90026505 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (lymphocyte) 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90026506 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (monocyte) 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 21 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90026507 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (neutrophil) 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 62 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90026508 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Platelet count 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 16 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90026509 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Mean platelet volume 16,201 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [NR] (imputed) 13 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90026510 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 42 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90026511 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (basophil) 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 6 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90026512 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (eosinophil) 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 6 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90026513 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (lymphocyte) 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 9 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90026514 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (monocyte) 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 17 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90026515 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (neutrophil) 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 30 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90026516 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Platelet count 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 1 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90026517 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Mean platelet volume 21,347 Hispanic or Latin American individuals NA Affymetrix, Illumina [NR] (imputed) 11 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90026518 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90026519 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. C-reactive protein NR [NR] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90029099 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. C-reactive protein NR [NR] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90029100 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Creatinine levels NR [NR] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90029101 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Creatinine levels NR [NR] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90029102 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Creatinine levels NR [NR] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90029103 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Cystatin C levels NR [NR] (imputed) 1 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90029104 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Cystatin C levels NR [NR] (imputed) 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90029105 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Cystatin C levels NR [NR] (imputed) 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90029106 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Direct bilirubin levels NR [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90029107 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Direct bilirubin levels NR [NR] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90029108 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Direct bilirubin levels NR [NR] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90029109 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Gamma glutamyl transferase levels NR [NR] (imputed) 1 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90029110 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Gamma glutamyl transferase levels NR [NR] (imputed) 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90029111 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Gamma glutamyl transferase levels NR [NR] (imputed) 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90029112 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Glucose levels NR [NR] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90029113 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Glucose levels NR [NR] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90029114 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Glucose levels NR [NR] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90029115 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Glycated hemoglobin HbA1c levels NR [NR] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90029116 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Glycated hemoglobin HbA1c levels NR [NR] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90029117 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Glycated hemoglobin HbA1c levels NR [NR] (imputed) 4 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90029118 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. High density lipoprotein cholesterol levels NR [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90029119 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. High density lipoprotein cholesterol levels NR [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90029120 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. High density lipoprotein cholesterol levels NR [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90029121 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Insulin-like growth factor 1 levels NR [NR] (imputed) 0 insulin-like growth factor I measurement http://www.ebi.ac.uk/efo/EFO_0801702 GCST90029122 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Insulin-like growth factor 1 levels NR [NR] (imputed) 0 insulin-like growth factor I measurement http://www.ebi.ac.uk/efo/EFO_0801702 GCST90029123 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Alanine aminotransferase levels NR [NR] (imputed) 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90029074 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Alanine aminotransferase levels NR [NR] (imputed) 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90029075 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Alanine aminotransferase levels NR [NR] (imputed) 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90029076 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum albumin levels NR [NR] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90029077 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum albumin levels NR [NR] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90029078 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum albumin levels NR [NR] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90029079 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum alkaline phosphatase levels NR [NR] (imputed) 1 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90029080 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum alkaline phosphatase levels NR [NR] (imputed) 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90029081 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum alkaline phosphatase levels NR [NR] (imputed) 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90029082 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Apolipoprotein A levels NR [NR] (imputed) 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90029083 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Apolipoprotein A levels NR [NR] (imputed) 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90029084 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Apolipoprotein A levels NR [NR] (imputed) 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90029085 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Apolipoprotein B levels NR [NR] (imputed) 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90029086 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Apolipoprotein B levels NR [NR] (imputed) 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90029087 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Apolipoprotein B levels NR [NR] (imputed) 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90029088 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Aspartate aminotransferase levels NR [NR] (imputed) 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90029089 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Aspartate aminotransferase levels NR [NR] (imputed) 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90029090 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Aspartate aminotransferase levels NR [NR] (imputed) 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90029091 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Calcium levels NR [NR] (imputed) 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90029092 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Calcium levels NR [NR] (imputed) 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90029093 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Calcium levels NR [NR] (imputed) 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90029094 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Total cholesterol levels NR [NR] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90029095 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Total cholesterol levels NR [NR] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90029096 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Total cholesterol levels NR [NR] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90029097 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. C-reactive protein NR [NR] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90029098 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Insulin-like growth factor 1 levels NR [NR] (imputed) 0 insulin-like growth factor I measurement http://www.ebi.ac.uk/efo/EFO_0801702 GCST90029124 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Direct low density lipoprotein cholesterol levels NR [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90029125 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Direct low density lipoprotein cholesterol levels NR [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90029126 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Direct low density lipoprotein cholesterol levels NR [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90029127 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Lipoprotein (a) levels NR [NR] (imputed) 1 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90029128 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Lipoprotein (a) levels NR [NR] (imputed) 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90029129 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Lipoprotein (a) levels NR [NR] (imputed) 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90029130 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Phosphate levels NR [NR] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90029131 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Phosphate levels NR [NR] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90029132 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Phosphate levels NR [NR] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90029133 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Sex hormone-binding globulin levels NR [NR] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90029134 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Sex hormone-binding globulin levels NR [NR] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90029135 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Sex hormone-binding globulin levels NR [NR] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90029136 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Testosterone levels NR [NR] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90029137 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Testosterone levels NR [NR] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90029138 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Testosterone levels NR [NR] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90029139 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Total bilirubin levels NR [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90029140 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Total bilirubin levels NR [NR] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90029141 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Total bilirubin levels NR [NR] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90029142 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum total protein levels NR [NR] (imputed) 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90029143 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum total protein levels NR [NR] (imputed) 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90029144 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Serum total protein levels NR [NR] (imputed) 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90029145 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Triglyceride levels NR [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90029146 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Triglyceride levels NR [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90029147 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Triglyceride levels NR [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90029148 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urate levels NR [NR] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90029149 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urate levels NR [NR] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90029150 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urate levels NR [NR] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90029151 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urea levels NR [NR] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90029152 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urea levels NR [NR] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90029153 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urea levels NR [NR] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90029154 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Vitamin D levels NR [NR] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90029155 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Vitamin D levels NR [NR] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90029156 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Vitamin D levels NR [NR] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90029157 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary creatinine levels NR [NR] (imputed) 1 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90029158 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary creatinine levels NR [NR] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90029159 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary creatinine levels NR [NR] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90029160 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary potassium levels NR [NR] (imputed) 1 urinary potassium measurement http://www.ebi.ac.uk/efo/EFO_0010952 GCST90029161 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary potassium levels NR [NR] (imputed) 0 urinary potassium measurement http://www.ebi.ac.uk/efo/EFO_0010952 GCST90029162 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary potassium levels NR [NR] (imputed) 0 urinary potassium measurement http://www.ebi.ac.uk/efo/EFO_0010952 GCST90029163 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary sodium levels NR [NR] (imputed) 1 urinary sodium measurement http://www.ebi.ac.uk/efo/EFO_0021522 GCST90029164 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary sodium levels NR [NR] (imputed) 0 urinary sodium measurement http://www.ebi.ac.uk/efo/EFO_0021522 GCST90029165 Genome-wide genotyping array 2023-01-26 34376796 Sun Q 2021-08-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34376796 Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Urinary sodium levels NR [NR] (imputed) 0 urinary sodium measurement http://www.ebi.ac.uk/efo/EFO_0021522 GCST90029166 Genome-wide genotyping array 2022-10-25 34586374 Giannakopoulou O 2021-09-29 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/34586374 The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. Depression 15,771 East Asian ancestry cases, 178,777 East Asian ancestry controls NA Affymetrix, Illumina [9223944] (imputed) 46 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90058032 Genome-wide genotyping array, Genome-wide sequencing 2022-10-25 34586374 Giannakopoulou O 2021-09-29 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/34586374 The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. Depression 12,027 East Asian ancestry cases, 83,727 East Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 16 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90058033 Genome-wide genotyping array, Genome-wide sequencing 2022-10-25 34586374 Giannakopoulou O 2021-09-29 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/34586374 The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. Depression 3,744 East Asian ancestry cases, 95,050 East Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 21 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90058034 Genome-wide genotyping array 2022-10-25 34586374 Giannakopoulou O 2021-09-29 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/34586374 The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. Clinical depression 8,223 East Asian ancestry cases, 85,370 East Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 22 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90058035 Genome-wide genotyping array, Genome-wide sequencing 2022-10-25 34586374 Giannakopoulou O 2021-09-29 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/34586374 The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. Depressive symptoms 6,124 East Asian ancestry cases, 73,095 East Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 8 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90058036 Genome-wide genotyping array, Genome-wide sequencing 2022-10-25 34586374 Giannakopoulou O 2021-09-29 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/34586374 The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. Depression 15,771 East Asian ancestry cases, 178,777 East Asian ancestry controls, 170,756 European ancestry cases, 329,443 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 43 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90058037 Genome-wide genotyping array, Genome-wide sequencing 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Acute dysphagia (moderate to severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Dysphagia http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015 GCST90102493 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Acute dysphagia (severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Dysphagia http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015 GCST90102494 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Mucositis (moderate to severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 2 response to radiation, mucositis http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_1001898 GCST90102495 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Late dysphagia (moderate to severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Dysphagia http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015 GCST90102496 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Late dysphagia (severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Dysphagia http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015 GCST90102497 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Xerostomia (moderate to severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, xerostomia http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0009869 GCST90102498 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Xerostomia (severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, xerostomia http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0009869 GCST90102499 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Fibrosis (moderate to severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, fibrosis http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0006890 GCST90102500 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Fibrosis (severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, fibrosis http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0006890 GCST90102501 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Fibrosis or atrophy (moderate to severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, fibrosis, Atrophy http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0006890, http://www.ebi.ac.uk/efo/EFO_1000096 GCST90102502 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Fibrosis or atrophy (severe) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, fibrosis, Atrophy http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0006890, http://www.ebi.ac.uk/efo/EFO_1000096 GCST90102503 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Tubefeeding at 6 months in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Tube feeding http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0033454 GCST90102504 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Standardised Total Average Toxicity (acute dysphagia or mucositis) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Dysphagia, mucositis http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015, http://www.ebi.ac.uk/efo/EFO_1001898 GCST90102505 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Standardised Total Average Toxicity (late dysphagia, xerostomia, fibrosis or atrophy) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Dysphagia, fibrosis, xerostomia, Atrophy http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015, http://www.ebi.ac.uk/efo/EFO_0006890, http://www.ebi.ac.uk/efo/EFO_0009869, http://www.ebi.ac.uk/efo/EFO_1000096 GCST90102506 Genome-wide genotyping array 2022-05-26 35039627 Schack LMH 2022-01-17 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/35039627 A genome-wide association study of radiotherapy induced toxicity in head and neck cancer patients identifies a susceptibility locus associated with mucositis. Standardised Total Average Toxicity (acute dysphagia, mucositis, late dysphagia, xerostomia, fibrosis or atrophy) in head and neck cancer treated with radiotherapy 1,183 European ancestry individuals 597 Dutch ancestry individuals Illumina [7178424] (imputed) 0 response to radiation, Dysphagia, fibrosis, xerostomia, Atrophy, mucositis http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015, http://www.ebi.ac.uk/efo/EFO_0006890, http://www.ebi.ac.uk/efo/EFO_0009869, http://www.ebi.ac.uk/efo/EFO_1000096, http://www.ebi.ac.uk/efo/EFO_1001898 GCST90102507 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Ruminococcus.s_Ruminococcus_lactaris) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027801 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Subdoligranulum.s_Subdoligranulum_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027802 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia.o_Erysipelotrichales.f_Erysipelotrichaceae.g_Erysipelotrichaceae_noname.s_Eubacterium_biforme) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027803 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia.o_Erysipelotrichales.f_Erysipelotrichaceae.g_Holdemania.s_Holdemania_filiformis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027804 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia.o_Erysipelotrichales.f_Erysipelotrichaceae.g_Holdemania.s_Holdemania_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027805 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Acidaminococcaceae.g_Phascolarctobacterium.s_Phascolarctobacterium_succinatutens) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027806 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Veillonellaceae.g_Dialister.s_Dialister_invisus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027807 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Veillonellaceae.g_Veillonella.s_Veillonella_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027808 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Burkholderiales_noname.g_Burkholderiales_noname.s_Burkholderiales_bacterium_1_1_47) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027809 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Oxalobacteraceae.g_Oxalobacter.s_Oxalobacter_formigenes) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027810 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Sutterellaceae.g_Parasutterella.s_Parasutterella_excrementihominis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027811 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Sutterellaceae.g_Sutterella.s_Sutterella_wadsworthensis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027812 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria.o_Desulfovibrionales.f_Desulfovibrionaceae.g_Bilophila.s_Bilophila_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027813 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria.o_Desulfovibrionales.f_Desulfovibrionaceae.g_Bilophila.s_Bilophila_wadsworthia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027814 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria.o_Desulfovibrionales.f_Desulfovibrionaceae.g_Desulfovibrio.s_Desulfovibrio_piger) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027815 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Enterobacteriales.f_Enterobacteriaceae.g_Escherichia.s_Escherichia_coli) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027816 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Enterobacteriales.f_Enterobacteriaceae.g_Escherichia.s_Escherichia_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027817 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Pasteurellales.f_Pasteurellaceae.g_Haemophilus.s_Haemophilus_parainfluenzae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027818 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Verrucomicrobia.c_Verrucomicrobiae.o_Verrucomicrobiales.f_Verrucomicrobiaceae.g_Akkermansia.s_Akkermansia_muciniphila) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027819 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_caccae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027820 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_cellulosilyticus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027821 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_clarus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027822 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_coprocola) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027823 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_dorei) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027824 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_eggerthii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027825 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes.s_Alistipes_indistinctus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027776 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes.s_Alistipes_onderdonkii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027777 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes.s_Alistipes_putredinis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027778 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes.s_Alistipes_senegalensis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027779 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes.s_Alistipes_shahii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027780 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes.s_Alistipes_sp_AP11) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027781 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Lactobacillaceae.g_Lactobacillus.s_Lactobacillus_delbrueckii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027782 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Streptococcaceae.g_Streptococcus.s_Streptococcus_parasanguinis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027783 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Streptococcaceae.g_Streptococcus.s_Streptococcus_salivarius) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027784 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Streptococcaceae.g_Streptococcus.s_Streptococcus_thermophilus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027785 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiaceae.g_Clostridium.s_Clostridium_asparagiforme) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027786 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiaceae.g_Clostridium.s_Clostridium_leptum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027787 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiales_noname.g_Flavonifractor.s_Flavonifractor_plautii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027788 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiales_noname.g_Pseudoflavonifractor.s_Pseudoflavonifractor_capillosus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027789 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae.g_Eubacterium.s_Eubacterium_eligens) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027790 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae.g_Eubacterium.s_Eubacterium_hallii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027791 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae.g_Eubacterium.s_Eubacterium_ramulus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027792 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae.g_Eubacterium.s_Eubacterium_rectale) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027793 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae.g_Eubacterium.s_Eubacterium_siraeum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027794 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae.g_Eubacterium.s_Eubacterium_ventriosum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027795 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Oscillospiraceae.g_Oscillibacter.s_Oscillibacter_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027796 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Faecalibacterium.s_Faecalibacterium_prausnitzii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027797 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Ruminococcaceae_noname.s_Ruminococcaceae_bacterium_D16) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027798 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Ruminococcus.s_Ruminococcus_bromii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027799 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Ruminococcus.s_Ruminococcus_callidus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027800 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027738 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027739 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027740 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia.o_Erysipelotrichales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027741 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027742 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027743 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria.o_Desulfovibrionales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027744 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Enterobacteriales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027745 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Pasteurellales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027746 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Verrucomicrobia.c_Verrucomicrobiae.o_Verrucomicrobiales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027747 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027748 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027749 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027750 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027751 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Verrucomicrobia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027752 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Actinomycetales.f_Micrococcaceae.g_Rothia.s_Rothia_mucilaginosa) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027753 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Bifidobacteriales.f_Bifidobacteriaceae.g_Bifidobacterium.s_Bifidobacterium_adolescentis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027754 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Bifidobacteriales.f_Bifidobacteriaceae.g_Bifidobacterium.s_Bifidobacterium_bifidum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027755 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Bifidobacteriales.f_Bifidobacteriaceae.g_Bifidobacterium.s_Bifidobacterium_catenulatum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027756 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Bifidobacteriales.f_Bifidobacteriaceae.g_Bifidobacterium.s_Bifidobacterium_longum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027757 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Adlercreutzia.s_Adlercreutzia_equolifaciens) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027758 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Collinsella.s_Collinsella_aerofaciens) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027759 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Eggerthella.s_Eggerthella_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027760 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Gordonibacter.s_Gordonibacter_pamelaeae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027761 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidales_noname.g_Bacteroidales_noname.s_Bacteroidales_bacterium_ph8) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027762 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Roseburia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027713 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Oscillospiraceae.g_Oscillibacter) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027714 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Anaerotruncus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027715 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Faecalibacterium) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027716 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Ruminococcaceae_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027717 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Ruminococcus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027718 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Ruminococcaceae.g_Subdoligranulum) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027719 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia.o_Erysipelotrichales.f_Erysipelotrichaceae.g_Erysipelotrichaceae_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027720 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Erysipelotrichia.o_Erysipelotrichales.f_Erysipelotrichaceae.g_Holdemania) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027721 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Acidaminococcaceae.g_Phascolarctobacterium) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027722 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Veillonellaceae.g_Dialister) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027723 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Negativicutes.o_Selenomonadales.f_Veillonellaceae.g_Veillonella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027724 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Burkholderiales_noname.g_Burkholderiales_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027725 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Oxalobacteraceae.g_Oxalobacter) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027726 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Sutterellaceae.g_Parasutterella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027727 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Sutterellaceae.g_Sutterellaceae_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027728 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Betaproteobacteria.o_Burkholderiales.f_Sutterellaceae.g_Sutterella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027729 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria.o_Desulfovibrionales.f_Desulfovibrionaceae.g_Bilophila) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027730 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Deltaproteobacteria.o_Desulfovibrionales.f_Desulfovibrionaceae.g_Desulfovibrio) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027731 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Enterobacteriales.f_Enterobacteriaceae.g_Escherichia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027732 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Proteobacteria.c_Gammaproteobacteria.o_Pasteurellales.f_Pasteurellaceae.g_Haemophilus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027733 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Verrucomicrobia.c_Verrucomicrobiae.o_Verrucomicrobiales.f_Verrucomicrobiaceae.g_Akkermansia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027734 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Actinomycetales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027735 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Bifidobacteriales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027736 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027737 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides.s_Bacteroides_faecis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027826 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Adlercreutzia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027689 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Collinsella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027690 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Eggerthella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027691 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Actinobacteria.c_Actinobacteria.o_Coriobacteriales.f_Coriobacteriaceae.g_Gordonibacter) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027692 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidaceae.g_Bacteroides) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027693 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Bacteroidales_noname.g_Bacteroidales_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027694 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Barnesiella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027695 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Coprobacter) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027696 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Odoribacter) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027697 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Parabacteroides) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027698 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Prevotellaceae.g_Paraprevotella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027699 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Prevotellaceae.g_Prevotella) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027700 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027701 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Lactobacillaceae.g_Lactobacillus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027702 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Bacilli.o_Lactobacillales.f_Streptococcaceae.g_Streptococcus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027703 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiaceae.g_Clostridium) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027704 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiales_noname.g_Flavonifractor) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027705 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Clostridiales_noname.g_Pseudoflavonifractor) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027706 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Eubacteriaceae.g_Eubacterium) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027707 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Blautia) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027708 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Butyrivibrio) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027709 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Coprococcus) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027710 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Dorea) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027711 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Firmicutes.c_Clostridia.o_Clostridiales.f_Lachnospiraceae.g_Lachnospiraceae_noname) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027712 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5676..acetyl.CoA.fermentation.to.butanoate.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027554 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5686..UMP.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027555 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5695..urate.biosynthesis.inosine.5..phosphate.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027556 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5705..allantoin.degradation.to.glyoxylate.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027557 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5791..1.4.dihydroxy.2.naphthoate.biosynthesis.II..plants.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027558 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5838..superpathway.of.menaquinol.8.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027559 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5850..superpathway.of.menaquinol.6.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027560 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5913..TCA.cycle.VI..obligate.autotrophs.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027561 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5918..superpathay.of.heme.biosynthesis.from.glutamate) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027562 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5920..superpathway.of.heme.biosynthesis.from.glycine) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027563 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5941..glycogen.degradation.II..eukaryotic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027564 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5971..palmitate.biosynthesis.II..bacteria.and.plants.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027565 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5973..cis.vaccenate.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027566 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5989..stearate.biosynthesis.II..bacteria.and.plants.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027567 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6121..5.aminoimidazole.ribonucleotide.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027568 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6123..inosine.5..phosphate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027569 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6125..superpathway.of.guanosine.nucleotides.de.novo.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027570 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.6147..6.hydroxymethyl.dihydropterin.diphosphate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027571 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Parabacteroides.s_Parabacteroides_merdae) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027769 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Porphyromonadaceae.g_Parabacteroides.s_Parabacteroides_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027770 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Prevotellaceae.g_Paraprevotella.s_Paraprevotella_clara) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027771 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Prevotellaceae.g_Paraprevotella.s_Paraprevotella_unclassified) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027772 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Prevotellaceae.g_Paraprevotella.s_Paraprevotella_xylaniphila) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027773 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Prevotellaceae.g_Prevotella.s_Prevotella_copri) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027774 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut microbiota abundance (k_Bacteria.p_Bacteroidetes.c_Bacteroidia.o_Bacteroidales.f_Rikenellaceae.g_Alistipes.s_Alistipes_finegoldii) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027775 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.2941..L.lysine.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027529 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.2942..L.lysine.biosynthesis.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027530 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.3001..superpathway.of.L.isoleucine.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027531 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.3781..aerobic.respiration.I..cytochrome.c.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027532 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.4242..pantothenate.and.coenzyme.A.biosynthesis.III) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027533 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.4984..urea.cycle) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027534 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY4FS.7..phosphatidylglycerol.biosynthesis.I..plastidic.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027535 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5005..biotin.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027536 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5022..4.aminobutanoate.degradation.V) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027537 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5088..L.glutamate.degradation.VIII..to.propanoate.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027538 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5097..L.lysine.biosynthesis.VI) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027539 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5100..pyruvate.fermentation.to.acetate.and.lactate.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027540 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5101..L.isoleucine.biosynthesis.II) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027541 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5104..L.isoleucine.biosynthesis.IV) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027542 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5121..superpathway.of.geranylgeranyl.diphosphate.biosynthesis.II..via.MEP.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027543 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5173..superpathway.of.acetyl.CoA.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027544 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5177..glutaryl.CoA.degradation) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027545 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5188..tetrapyrrole.biosynthesis.I..from.glutamate.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027546 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5189..tetrapyrrole.biosynthesis.II..from.glycine.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027547 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5345..superpathway.of.L.methionine.biosynthesis..by.sulfhydrylation.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027548 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5384..sucrose.degradation.IV..sucrose.phosphorylase.) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027549 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5505..L.glutamate.and.L.glutamine.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027550 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5656..mannosylglycerate.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027551 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5659..GDP.mannose.biosynthesis) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027552 Genome-wide genotyping array 2022-07-01 35115690 Lopera-Maya EA 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115690 Effect of host genetics on the gut microbiome in 7,738 participants of the Dutch Microbiome Project. Gut bacterial pathway abundance (PWY.5667..CDP.diacylglycerol.biosynthesis.I) 7,738 European ancestry individuals NA Illumina [5584686] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90027553 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FEV1) 100,285 Chinese ancestry individuals NA Affymetrix [NR] (imputed) 27 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90054783 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FVC) 100,285 Chinese ancestry individuals NA Affymetrix [NR] (imputed) 8 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90054784 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FEV1/FVC) 100,285 Chinese ancestry individuals NA Affymetrix [NR] (imputed) 6 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90054785 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FEV1) and body mass index up to 100,285 Chinese ancestry individuals up to 457,756 European ancestry individuals Affymetrix [NR] (imputed) 7 forced expiratory volume, body mass index http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90054786 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FEV1) and waist to hip ratio adjusted for BMI up to 100,285 Chinese ancestry individuals up to 457,756 European ancestry individuals Affymetrix [NR] (imputed) 5 BMI-adjusted waist-hip ratio, forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0004314 GCST90054787 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FEV1) and waist circumference adjusted for BMI up to 100,285 Chinese ancestry individuals up to 457,756 European ancestry individuals Affymetrix [NR] (imputed) 7 BMI-adjusted waist circumference, forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0007789, http://www.ebi.ac.uk/efo/EFO_0004314 GCST90054788 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FVC) and body mass index up to 100,285 Chinese ancestry individuals up to 457,756 European ancestry individuals Affymetrix [NR] (imputed) 4 body mass index, vital capacity http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004312 GCST90054789 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FVC) and waist to hip ratio adjusted for BMI up to 100,285 Chinese ancestry individuals up to 457,756 European ancestry individuals Affymetrix [NR] (imputed) 1 BMI-adjusted waist-hip ratio, vital capacity http://www.ebi.ac.uk/efo/EFO_0007788, http://www.ebi.ac.uk/efo/EFO_0004312 GCST90054790 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FVC) and waist circumference adjusted for BMI up to 100,285 Chinese ancestry individuals up to 457,756 European ancestry individuals Affymetrix [NR] (imputed) 1 BMI-adjusted waist circumference, vital capacity http://www.ebi.ac.uk/efo/EFO_0007789, http://www.ebi.ac.uk/efo/EFO_0004312 GCST90054791 Genome-wide genotyping array 2021-11-08 33766948 Zhu Z 2021-03-25 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33766948 A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. Lung function (FEV1/FVC) and body mass index up to 100,285 Chinese ancestry individuals up to 457,756 European ancestry individuals Affymetrix [NR] (imputed) 0 body mass index, FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004713 GCST90054792 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Fibrinopeptide B (1-12) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095576 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Fibrinopeptide B (1-13) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095629 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Threonylphenylalanine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095632 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 3-aminoisobutyrate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90095534 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5-oxoproline levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90095562 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5-methyluridine (ribothymidine) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90095646 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Succinylcarnitine (C4DC) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90095623 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetyltyrosine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90095510 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Cis-4-decenoate (10:1n6) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095487 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-linoleoylglycine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095489 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-linoleoyltaurine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095490 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-palmitoylglycine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095491 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 10-undecenoate (11:1n1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095492 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Hexanoylcarnitine (C6) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095493 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Cis-4-decenoylcarnitine (C10:1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095494 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Nonanoylcarnitine (C9) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095495 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Octanoylcarnitine (c8) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095496 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Methylmalonate (mma) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095499 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetyl-2-aminooctanoate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095511 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 2-aminooctanoate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095516 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Cholic acid glucuronide levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095531 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Deoxycholic acid glucuronide levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095533 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095536 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5alpha-pregnan-diol disulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095538 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Arachidonoylcarnitine (C20:4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095543 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Etiocholanolone glucuronide levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095595 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Butyrylcarnitine (C4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095598 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Butyrylglycine (C4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095599 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-linoleoyl-GPG (18:2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095601 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-oleoyl-GPG (18:1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095602 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Glycochenodeoxycholate glucuronide (1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095603 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Taurodeoxycholic acid 3-sulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095604 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Hexadecanedioate (C16) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095606 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Hexadecenedioate (C16:1-DC) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095607 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Octadecenedioate (C18:1-DC) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095608 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Octadecadienedioate (C18:2-DC) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095609 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Deoxycarnitine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095610 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095614 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095615 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Decadienedioic acid (C10:2-DC) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095616 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Tetradecadienedioate (C14:2-DC) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095617 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095619 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095620 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095621 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-palmitoyl-GPE (16:0) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095622 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Androstenediol (3beta,17beta) disulfate (1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095636 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Pregnen-diol disulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095637 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Pregnenetriol disulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095638 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Androstenediol (3alpha, 17alpha) monosulfate (2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095640 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5alpha-androstan-3beta,17beta-diol monosulfate (1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095641 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Dihomo-linolenoylcarnitine (C20:3n3 or 6) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095544 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Dihomo-linoleoylcarnitine (C20:2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095545 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Azelaoyltaurine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095546 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Hexanoylglutamine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095550 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5alpha-androstan-3alpha,17alpha-diol monosulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095555 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095556 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095557 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Androsterone sulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095558 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Epiandrosterone sulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095559 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Carnitine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095577 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095580 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1,2-dilinoleoyl-GPC (18:2/18:2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095581 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Docosatrienoate (22:3n6) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095582 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Stearoyl-arachidonoyl-glycerol (18:0/20:4) [1] levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095583 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-linoleoyl-GPE (18:2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095584 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095585 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095586 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-arachidonoyl-GPC (20:4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095587 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095588 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095589 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Oleoyl-arachidonoyl-glycerol (18:1/20:4) [1] levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095590 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Oleoyl-arachidonoyl-glycerol (18:1/20:4) [2] levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095591 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095592 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 17alpha-hydroxypregnanolone glucuronide levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095593 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Androsterone glucuronide levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095594 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095642 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Bilirubin levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90095506 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Bilirubin (E,E) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90095507 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Bilirubin (E,Z or Z,E) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90095508 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 4-guanidinobutanoate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095488 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Imidazole lactate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095498 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 3-methylglutaconate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095500 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 3-methylglutarylcarnitine (2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095501 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylkynurenine (2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095512 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylhistidine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095513 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylleucine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095514 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylphenylalanine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095515 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. High light scatter reticulocyte count 437,723 European ancestry individuals NA NR [9800000] (imputed) 29 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90025970 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Immature fraction of reticulocytes 438,154 European ancestry individuals NA NR [9800000] (imputed) 9 Immature Reticulocyte Fraction Measurement http://www.ebi.ac.uk/efo/EFO_0009253 GCST90025971 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Reticulocyte count 437,291 European ancestry individuals NA NR [9800000] (imputed) 31 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90025972 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Bilirubin levels 436,055 European ancestry individuals NA NR [9800000] (imputed) 16 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90025973 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Hemoglobin A1c levels 437,749 European ancestry individuals NA NR [9800000] (imputed) 36 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90025974 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Mean reticulocyte volume 436,944 European ancestry individuals NA NR [9800000] (imputed) 19 mean reticulocyte volume http://www.ebi.ac.uk/efo/EFO_0010701 GCST90025975 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Mean sphered cell volume 437,736 European ancestry individuals NA NR [9800000] (imputed) 22 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90025976 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Neutrophil count 443,782 European ancestry individuals NA NR [9800000] (imputed) 13 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90025977 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Lung function (FEV1/FVC) 371,898 European ancestry individuals NA NR [9800000] (imputed) 4 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90025978 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Alanine aminotransferase levels 437,724 European ancestry individuals NA NR [9800000] (imputed) 20 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90025979 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Aspartate aminotransferase levels 436,275 European ancestry individuals NA NR [9800000] (imputed) 14 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90025980 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Diastolic blood pressure 422,713 European ancestry individuals NA NR [9800000] (imputed) 7 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90025981 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Heel bone mineral density T score 445,855 European ancestry individuals NA NR [9800000] (imputed) 11 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90025982 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Direct bilirubin levels 372,420 European ancestry individuals NA NR [9800000] (imputed) 8 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90025983 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Lymphocyte count 443,762 European ancestry individuals NA NR [9800000] (imputed) 16 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90025984 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. White blood cell count 444,734 European ancestry individuals NA NR [9800000] (imputed) 17 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90025985 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Blood glucose levels 400,458 European ancestry individuals NA NR [9800000] (imputed) 6 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90025986 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Eosinophil counts 440,275 European ancestry individuals NA NR [9800000] (imputed) 14 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90025987 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Red cell distribution width 441,263 European ancestry individuals NA NR [9800000] (imputed) 24 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90025988 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Insulin-like growth factor 1 levels 435,516 European ancestry individuals NA NR [9800000] (imputed) 29 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90025989 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Calcium levels 400,792 European ancestry individuals NA NR [9800000] (imputed) 7 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90025990 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Serum urea levels 437,580 European ancestry individuals NA NR [9800000] (imputed) 3 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90025991 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Serum albumin levels 400,938 European ancestry individuals NA NR [9800000] (imputed) 10 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90025992 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Lipoprotein (a) levels 348,806 European ancestry individuals NA NR [9800000] (imputed) 7 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90025993 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Body mass index 457,756 European ancestry individuals NA NR [9800000] (imputed) 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90025994 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Serum total protein levels 400,482 European ancestry individuals NA NR [9800000] (imputed) 9 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90025995 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Waist-to-hip ratio adjusted for BMI 458,349 European ancestry individuals NA NR [9800000] (imputed) 4 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90025996 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Basophil count 438,607 European ancestry individuals NA NR [9800000] (imputed) 3 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90025997 Genome-wide genotyping array 2021-11-16 34226706 Barton AR 2021-07-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34226706 Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses. Lung function (FVC) 371,898 European ancestry individuals NA NR [9800000] (imputed) 3 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90025998 Genome-wide genotyping array 2021-11-17 34535985 Fairfield CJ 2021-09-17 Hepatol Commun www.ncbi.nlm.nih.gov/pubmed/34535985 Genome-Wide Association Study of NAFLD Using Electronic Health Records. Nonalcoholic fatty liver disease 4,761 European ancestry cases, 373,227 European ancestry controls 2,656 European ancestry cases, 32,602 European ancestry controls Affymetrix [9723654] (imputed) 6 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90054782 Genome-wide genotyping array 2021-10-22 34445011 Park S 2021-08-19 Nutrients www.ncbi.nlm.nih.gov/pubmed/34445011 Association between Polygenetic Risk Scores of Low Immunity and Interactions between These Scores and Moderate Fat Intake in a Large Cohort. Low white blood cell count 4,176 Korean ancestry low WBC count cases, 36,551 Korean ancestry high WBC count controls 207 Korean ancestry low WBC count cases, 5,286 Korean ancestry high WBC count controls Affymetrix [NR] 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90029071 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hip or knee up to 400,604 European, Japanese ancestry female cases, up to 490,345 European, Japanese ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hip, osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616 GCST90061021 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (hip) up to 36,445 European ancestry female cases, up to 316,943 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90061022 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Knee osteoarthritis up to 333,557 European, Japanese ancestry female cases, up to 396,054 European, Japanese ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90061023 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (with total hip replacement) up to 23,021 European, East Asian ancestry female cases, up to 296,016 European, East Asian ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 2 total hip arthroplasty, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0009806, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90034531 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (with total knee replacement) up to 18,200 European ancestry female cases, up to 233,841 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, knee, total joint arthroplasty http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0010726 GCST90061024 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hip or knee (with total joint replacement) up to 40,887 European ancestry female cases, up to 327,689 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hip, osteoarthritis, knee, total joint arthroplasty http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0010726 GCST90061025 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hand up to 20,901 European ancestry female cases, up to 282,881 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90061026 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Finger osteoarthritis up to 10,804 European ancestry female cases, up to 255,814 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90061027 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Thumb osteoarthritis up to 10,536 European ancestry female cases, up to 236,919 European ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90061028 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Spine osteoarthritis up to 305,578 East Asian ancestry female cases, up to 333,950 East Asian ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, spine http://www.ebi.ac.uk/efo/EFO_1000787 GCST90061029 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis up to 56,462 European, East Asian ancestry male cases, up to 153,808 European ancestry European, East Asian ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90061030 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hip or knee up to 400,604 Japanese, European ancestry male cases, up to 490,345 Japanese, European ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hip, osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616 GCST90061031 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (hip) up to 36,445 European ancestry male cases, up to 316,943 European ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90061032 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Knee osteoarthritis up to 333,557 European, Japanese ancestry male cases, up to 396,054 European, Japanese ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90061033 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (with total hip replacement) 23,021 European, East Asian ancestry male cases, 296,016 European, East Asian ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 total hip arthroplasty, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0009806, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90061034 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (with total knee replacement) up to 18,200 European ancestry male cases, up to 233,841 European ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, knee, total joint arthroplasty http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0010726 GCST90061035 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hip or knee (with total joint replacement) up to 40,887 European ancestry male cases, up to 327,689 European ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hip, osteoarthritis, knee, total joint arthroplasty http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0010726 GCST90061036 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hand up to 20,901 European ancestry male cases, up to 282,881 European ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90061037 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Finger osteoarthritis up to 10,804 European ancestry male cases, up to 255,814 European ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90061038 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Thumb osteoarthritis up to 10,536 European ancestry male cases, up to 236,919 European ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90061039 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Spine osteoarthritis up to 305,578 European, East Asian ancestry male cases, up to 333,950 European, East Asian ancestry male controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, spine http://www.ebi.ac.uk/efo/EFO_1000787 GCST90061040 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hip or knee 88,842 European ancestry cases, 397,208 European ancestry controls, 899 Japanese ancestry cases, 3,396 Japanese ancestry controls NA Affymetrix, Illumina [NR] (imputed) 16 osteoarthritis, hip, osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616 GCST90034521 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis 175,803 European ancestry cases, 644,862 European ancestry controls, 1,265 Japanese ancestry cases, 449 Southern Chinese ancestry cases, 3,330 Japanese ancestry controls, 981 Southern Chinese ancestry controls NA Affymetrix, Illumina [NR] (imputed) 11 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90034520 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (hip) 36,445 European ancestry cases, 316,943 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 11 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90034522 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Knee osteoarthritis 61,588 European ancestry cases, 330,161 European ancestry controls, 899 Japanese ancestry cases, 3,396 Japanese ancestry controls NA Affymetrix, Illumina [NR] (imputed) 10 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90034523 Genome-wide genotyping array 2021-06-21 34027909 Cox CK 2021-05-22 Female Pelvic Med Reconstr Surg www.ncbi.nlm.nih.gov/pubmed/34027909 Genome-Wide Association Study of Pelvic Organ Prolapse Using the Michigan Genomics Initiative. Pelvic organ prolapse (need for surgery) 767 European ancestry cases, 16,383 European ancestry controls NA Illumina [> 20000000] (imputed) 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST011944 Genome-wide genotyping array 2021-06-21 34027909 Cox CK 2021-05-22 Female Pelvic Med Reconstr Surg www.ncbi.nlm.nih.gov/pubmed/34027909 Genome-Wide Association Study of Pelvic Organ Prolapse Using the Michigan Genomics Initiative. Pelvic organ prolapse 1,329 European ancestry cases, 16,383 European ancestry controls NA Illumina [> 20000000] (imputed) 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST011945 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (with total hip replacement) 23,021 European ancestry cases, 296,016 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 27 total hip arthroplasty, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0009806, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90034524 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis (with total knee replacement) 18,200 European ancestry cases, 233,841 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 osteoarthritis, knee, total joint arthroplasty http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0010726 GCST90034525 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hip or knee (with total joint replacement) 40,887 European ancestry cases, 327,689 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 13 osteoarthritis, hip, osteoarthritis, knee, total joint arthroplasty http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0010726 GCST90034526 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis of the hand 20,901 European ancestry cases, 282,881 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 5 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90034527 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Finger osteoarthritis 10,804 European ancestry cases, 255,814 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90034528 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Thumb osteoarthritis 10,536 European ancestry cases, 236,919 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 1 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90034529 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Spine osteoarthritis 27,557 European ancestry cases, 301,266 European ancestry controls, 366 Japanese ancestry cases, 3331 Japanese ancestry controls, 449 Southern Chinese ancestry cases, 981 Southern Chinese ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 osteoarthritis, spine http://www.ebi.ac.uk/efo/EFO_1000787 GCST90034530 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Early-onset osteoarthritis 6,838 European ancestry cases, 41,449 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 1 age of onset of osteoarthritis http://purl.obolibrary.org/obo/OBA_2001008 GCST90034533 Genome-wide genotyping array 2021-11-01 34450027 Boer CG 2021-08-24 Cell www.ncbi.nlm.nih.gov/pubmed/34450027 Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations. Osteoarthritis 90,838 European, East Asian ancestry female cases, 192,697 European, East Asian ancestry female controls NA Affymetrix, Illumina [NR] (imputed) 1 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90034532 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Depression x vitamin D interaction 52,766 European ancestry cases, 57,978 European ancestry controls NA Affymetrix [NR] (imputed) 0 unipolar depression, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085905 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Depression x vitamin D PRS interaction (COJO adjusted) 58,349 European ancestry cases, 63,336 European ancestry controls NA Affymetrix [NR] (imputed) 1 unipolar depression, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085906 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Depression x vitamin D PRS interaction 58,349 European ancestry cases, 63,336 European ancestry controls NA Affymetrix [NR] (imputed) 0 unipolar depression, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085907 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Anxiety x vitamin D interaction 19,759 European ancestry cases, 79,025 European ancestry controls NA Affymetrix [NR] (imputed) 0 anxiety, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085908 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Anxiety x vitamin D PRS interaction (COJO adjusted) 21,807 European ancestry cases, 86,502 European ancestry controls NA Affymetrix [NR] (imputed) 1 anxiety, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085909 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Anxiety x vitamin D PRS interaction 21,807 European ancestry cases, 86,502 European ancestry controls NA Affymetrix [NR] (imputed) 0 anxiety, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085910 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Depression score x vitamin D interaction 109,543 European ancestry individuals NA Affymetrix [NR] (imputed) 1 unipolar depression, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085911 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Depression score x vitamin D PRS interaction (COJO adjusted) 120,033 European ancestry individuals NA Affymetrix [NR] (imputed) 0 unipolar depression, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085912 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Depression score x vitamin D PRS interaction 120,033 European ancestry individuals NA Affymetrix [NR] (imputed) 0 unipolar depression, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085913 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Anxiety score x vitamin D interaction 110,023 European ancestry individuals NA Affymetrix [NR] (imputed) 2 anxiety, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085914 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Anxiety score x vitamin D PRS interaction (COJO adjusted) 120,590 European ancestry individuals NA Affymetrix [NR] (imputed) 3 anxiety, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085915 Genome-wide genotyping array 2022-01-06 34684344 Zhang Z 2021-09-24 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684344 Vitamin D and the Risks of Depression and Anxiety: An Observational Analysis and Genome-Wide Environment Interaction Study. Anxiety score x vitamin D PRS interaction 120,590 European ancestry individuals NA Affymetrix [NR] (imputed) 4 anxiety, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90085916 Genome-wide genotyping array 2021-09-06 34330890 Ip HF 2021-07-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34330890 Genetic association study of childhood aggression across raters, instruments, and age. Childhood aggressive behavior 87,485 European ancestry individuals NA Affymetrix, Illumina [up to 7284995] (imputed) 49 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST90027070 Genome-wide genotyping array 2021-09-06 34330890 Ip HF 2021-07-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34330890 Genetic association study of childhood aggression across raters, instruments, and age. Childhood aggressive behavior (reported by father) 87,485 European ancestry individuals NA Affymetrix, Illumina [up to 7284995] (imputed) 0 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST90027071 Genome-wide genotyping array 2021-09-06 34330890 Ip HF 2021-07-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34330890 Genetic association study of childhood aggression across raters, instruments, and age. Childhood aggressive behavior (reported by mother) 87,485 European ancestry individuals NA Affymetrix, Illumina [up to 7284995] (imputed) 0 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST90027072 Genome-wide genotyping array 2021-09-06 34330890 Ip HF 2021-07-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34330890 Genetic association study of childhood aggression across raters, instruments, and age. Childhood aggressive behavior (self reported) 87,485 European ancestry individuals NA Affymetrix, Illumina [up to 7284995] (imputed) 0 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST90027073 Genome-wide genotyping array 2021-09-06 34330890 Ip HF 2021-07-30 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34330890 Genetic association study of childhood aggression across raters, instruments, and age. Childhood aggressive behavior (reported by teacher) 87,485 European ancestry individuals NA Affymetrix, Illumina [up to 7284995] (imputed) 0 childhood aggressive behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007663 GCST90027074 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bleeding gums (UKB data field 6149) 59,427 European ancestry cases, 115,782 European ancestry controls NA Affymetrix, Illumina [286891] 0 Gingival bleeding http://purl.obolibrary.org/obo/HP_0000225 GCST90079438 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R12: dyspepsia indigestion (Gene-based burden) 792 European ancestry cases, 328,260 European ancestry controls NA Illumina [184145] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90081896 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Dentures (UKB data field 6149) 74,437 European ancestry cases, 100,772 European ancestry controls NA Affymetrix, Illumina [286891] 0 dentures http://www.ebi.ac.uk/efo/EFO_0010078 GCST90079441 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ear vestibular disorder (Gene-based burden) 3,950 European ancestry cases, 327,804 European ancestry controls NA Illumina [184201] 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90081820 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Loose teeth (UKB data field 6149) 18,873 European ancestry cases, 156,336 European ancestry controls NA Affymetrix, Illumina [286891] 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90079439 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81: ear vestibular disorder (Gene-based burden) 3,505 European ancestry cases, 325,547 European ancestry controls NA Illumina [184145] 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90081821 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mouth ulcers (UKB data field 6149) 46,301 European ancestry cases, 128,908 European ancestry controls NA Affymetrix, Illumina [286891] 0 Oral ulcer http://purl.obolibrary.org/obo/HP_0000155 GCST90079436 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eczema or dermatitis (Gene-based burden) 12,790 European ancestry cases, 318,964 European ancestry controls NA Illumina [184201] 0 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90081839 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Painful gums (UKB data field 6149) 13,435 European ancestry cases, 161,774 European ancestry controls NA Affymetrix, Illumina [286891] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90079437 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L30: Eczema or dermatitis (Gene-based burden) 10,233 European ancestry cases, 318,819 European ancestry controls NA Illumina [184145] 0 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90081840 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Toothache (UKB data field 6149) 19,161 European ancestry cases, 156,048 European ancestry controls NA Affymetrix, Illumina [286891] 0 toothache http://www.ebi.ac.uk/efo/EFO_0010072 GCST90079440 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Emphysema chronic bronchitis (Gene-based burden) 6,252 European ancestry cases, 325,502 European ancestry controls NA Illumina [184201] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90081661 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse wave Arterial Stiffness index (UKB data field 21021) 172,449 European ancestry individuals NA Affymetrix, Illumina [286601] 0 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST90078687 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J43: emphysema chronic bronchitis (Gene-based burden) 5,961 European ancestry cases, 323,091 European ancestry controls NA Illumina [184145] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90081662 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50.8: Other specified disorders of male genital organs 3,016 European ancestry cases, 171,235 European ancestry controls NA Affymetrix, Illumina [286378] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90080634 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Endometriosis (Gene-based burden) 3,711 European ancestry cases, 328,043 European ancestry controls NA Illumina [184193] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90081807 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 714 (UKB data field 4946) 1,083 European ancestry cases, 170,999 European ancestry controls NA Affymetrix, Illumina [285879] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079234 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80: Endometriosis (Gene-based burden) 3,142 European ancestry cases, 174,752 European ancestry controls NA Illumina [177166] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90081808 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 987 (UKB data field 4946) 170,897 European ancestry cases, 1,185 European ancestry controls NA Affymetrix, Illumina [285879] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079235 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Enlarged prostate (Gene-based burden) 7,026 European ancestry cases, 324,728 European ancestry controls NA Illumina [184194] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90081803 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D29: Benign neoplasm of male genital organs 1,184 European ancestry cases, 172,279 European ancestry controls NA Affymetrix, Illumina [285314] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079691 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N40: enlarged prostate (Gene-based burden) 6,347 European ancestry cases, 144,811 European ancestry controls NA Illumina [172888] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90081804 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N45: Orchitis and epididymitis 1,983 European ancestry cases, 171,102 European ancestry controls NA Affymetrix, Illumina [284915] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90080626 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Epilepsy (Gene-based burden) 3,591 European ancestry cases, 328,163 European ancestry controls NA Illumina [184201] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90081729 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - adult (UKB data field 4957) 147,135 European ancestry cases, 24,190 European ancestry controls NA Affymetrix, Illumina [284819] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079238 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 116) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012995 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 117) 19,670 European ancestry individuals NA NR [9705931] (imputed) 9 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012996 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 118) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012997 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 119) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012998 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 120) 19,670 European ancestry individuals NA NR [9705931] (imputed) 5 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012999 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 121) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013000 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 122) 19,670 European ancestry individuals NA NR [9705931] (imputed) 6 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013001 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 123) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013002 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 124) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013003 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 125) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013004 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 126) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013005 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 127) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013006 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 128) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013007 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 129) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013008 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 130) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013009 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 131) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013010 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 132) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013011 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 133) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013012 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 134) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013013 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 135) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013014 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 136) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013015 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 137) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013016 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 138) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013017 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 139) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013018 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 140) 19,670 European ancestry individuals NA NR [9705931] (imputed) 7 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013019 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 190) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013069 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 191) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013070 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 192) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013071 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 193) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013072 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 194) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013073 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 195) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013074 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 196) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013075 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 197) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013076 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 198) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013077 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 199) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013078 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 200) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013079 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 201) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013080 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 202) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013081 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 203) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013082 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 204) 19,670 European ancestry individuals NA NR [9705931] (imputed) 4 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013083 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 205) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013084 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 206) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013085 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 207) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013086 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 208) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013087 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 209) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013088 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 210) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013089 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 211) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013090 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 212) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013091 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 213) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013092 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 214) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013093 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 215) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013094 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 216) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013095 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 217) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013096 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 218) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013097 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 219) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013098 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 220) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013099 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 221) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013100 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 222) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013101 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 223) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013102 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 224) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013103 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 225) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013104 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 226) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013105 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 227) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013106 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 228) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013107 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 229) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013108 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 230) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013109 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 231) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013110 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 232) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013111 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 233) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013112 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 234) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013113 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 235) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013114 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 236) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013115 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 237) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013116 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 238) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013117 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 239) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013118 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 141) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013020 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 142) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013021 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 143) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013022 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 144) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013023 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 145) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013024 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 146) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013025 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 147) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013026 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 148) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013027 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 149) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013028 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 150) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013029 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 151) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013030 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 152) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013031 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 153) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013032 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 154) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013033 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 155) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013034 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 156) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013035 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 157) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013036 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 158) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013037 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 159) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013038 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 160) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013039 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 161) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013040 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 162) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013041 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 163) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013042 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 164) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013043 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 90) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012969 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 91) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012970 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 92) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012971 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 93) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012972 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 94) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012973 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 95) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012974 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 96) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012975 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 97) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012976 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 98) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012977 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 99) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012978 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 100) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012979 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 101) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012980 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 102) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012981 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 103) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012982 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 104) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012983 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 105) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012984 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 106) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012985 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 107) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012986 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 108) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012987 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 109) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012988 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 110) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012989 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 111) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012990 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 112) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012991 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 113) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012992 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 114) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012993 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 115) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012994 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 165) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013044 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 166) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013045 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 167) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013046 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 168) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013047 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 169) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013048 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 170) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013049 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 171) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013050 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 172) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013051 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 173) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013052 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 174) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013053 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 175) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013054 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 176) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013055 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 177) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013056 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 178) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013057 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 179) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013058 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 180) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013059 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 181) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013060 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 182) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013061 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 183) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013062 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 184) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013063 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 185) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013064 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 186) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013065 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 187) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013066 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 188) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013067 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 189) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013068 Genome-wide genotyping array 2021-05-04 32965087 Zamanpoor M 2020-09-23 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/32965087 The genetic basis for the inverse relationship between rheumatoid arthritis and schizophrenia. Rheumatoid arthritis or schizophrenia 29,880 European and Asian ancestry rheumatoid arthritis cases, 7,699 Chinese ancestry schizophrenia cases, 35,476 schizophrenia cases, 73,758 European and Asian ancestry controls, 18,327 Chinese ancestry controls, 46,839 controls NA NR [1483435] 0 rheumatoid arthritis, schizophrenia http://www.ebi.ac.uk/efo/EFO_0000685, http://purl.obolibrary.org/obo/MONDO_0005090 GCST011619 Genome-wide genotyping array 2021-04-30 32958699 Innocenti F 2020-09-21 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/32958699 Genomic analysis of germline variation associated with survival of colorectal cancer patients treated with chemotherapy plus biologics in CALGB/SWOG 80405 (Alliance). Metastatic colorectal cancer survival in treatment with chemotherapy plus biologics 613 European ancestry individuals NA Illumina [540021] 6 metastatic colorectal cancer, survival time http://www.ebi.ac.uk/efo/EFO_1001480, http://www.ebi.ac.uk/efo/EFO_0000714 GCST011584 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOE 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90088999 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOF 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086939 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088827 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087825 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA6 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089003 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA7 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087832 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA9 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087544 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AOC1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089296 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AOC2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089424 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AP1G2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087179 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AP2A2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087566 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AP4M1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086219 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APAF1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087542 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APBB1 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087251 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APBB1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087835 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APBB2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087205 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APBB2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087211 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APBB3 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087224 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APBB3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087545 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APCDD1 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089520 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APCS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087947 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APEX1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090861 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APLN 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089533 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APLP1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089739 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APLP2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086377 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Atrial fibrillation (chronic vs. intermittent) 340 German ancestry individuals NA Affymetrix [577007] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90012174 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Atrial fibrillation 2,798 German ancestry individuals NA Affymetrix [577007] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90012175 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Coronary artery disease 2,824 German ancestry individuals NA Affymetrix [577007] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90012176 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Cancer 2,821 German ancestry individuals NA Affymetrix [577007] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90012177 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Cardiomyopathy 2,824 German ancestry individuals NA Affymetrix [577007] 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST90012178 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Death 2,824 German ancestry individuals NA Affymetrix [577007] 0 age at death http://www.ebi.ac.uk/efo/EFO_0005056 GCST90012179 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Diabetes mellitus 2,824 German ancestry individuals NA Affymetrix [577007] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90012180 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Type 2 diabetes 2,824 German ancestry individuals NA Affymetrix [577007] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90012181 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Arterial hypertension (history of) 2,824 German ancestry individuals NA Affymetrix [577007] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90012182 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Treatment with insulin 2,811 German ancestry individuals NA Affymetrix [577007] 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90012183 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Peripheral vascular disease 2,824 German ancestry individuals NA Affymetrix [577007] 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90012184 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Arrhythmia 2,789 German ancestry individuals NA Affymetrix [577007] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90012185 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Stroke 2,824 German ancestry individuals NA Affymetrix [577007] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90012186 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Valve disease 2,824 German ancestry individuals NA Affymetrix [577007] 0 heart valve disease http://www.ebi.ac.uk/efo/EFO_0009551 GCST90012187 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Venous thrombosis or pulmonary embolism 2,817 German ancestry individuals NA Affymetrix [577007] 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90012188 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Saturated fatty acid levels (palmitic acid C16:0) 2,776 German ancestry individuals NA Affymetrix [577007] 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90012189 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Saturated fatty acid levels (stearic acid C18:0) 2,776 German ancestry individuals NA Affymetrix [577007] 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90012190 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Polyunsaturated omega-3 fatty acid levels (DHA C22:6n3) 2,776 German ancestry individuals NA Affymetrix [577007] 0 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90012191 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Saturated fatty acid levels (myristic acid C14:0) 2,776 German ancestry individuals NA Affymetrix [577007] 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90012192 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Exogenous monosaturated fatty acid levels (trans-palmitoleic acid C16:1n7t) 2,776 German ancestry individuals NA Affymetrix [577007] 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90012193 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Monounsaturated omega-9 fatty acid levels (oleic acid C18:1n9) 2,776 German ancestry individuals NA Affymetrix [577007] 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90012194 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Trans-fatty acid levels (9-trans 12-trans octadecanoic acid, linolelaidic acid C18:2n6tt) 2,776 German ancestry individuals NA Affymetrix [577007] 0 trans fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0006821 GCST90012195 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Trans-fatty acid levels (9-cis 12-trans octadecanoic acid C18:2n6ct) 2,776 German ancestry individuals NA Affymetrix [577007] 0 trans fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0006821 GCST90012196 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Trans-fatty acid levels (9-trans 12-cis octadecanoic acid C18:2n6tc) 2,776 German ancestry individuals NA Affymetrix [577007] 0 trans fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0006821 GCST90012197 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Polyunsaturated omega-6 fatty acid levels (linoleic acid C18:2n6) 2,776 German ancestry individuals NA Affymetrix [577007] 0 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90012198 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGD 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088622 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGF 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088226 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGK1 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088877 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGK2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087667 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGLYRP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087752 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGLYRP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088320 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGLYRP2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089084 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGLYRP3 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086342 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGM1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090533 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGRMC1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089885 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGRMC2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086311 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGRMC2 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086379 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGRMC2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090259 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PHF3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086787 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PHGDH 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090429 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PI15 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089190 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PI3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088842 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIANP 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087795 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIANP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090772 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIAS3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087496 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIAS4 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086232 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIEZO1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086875 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIGA 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086332 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIGR 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088276 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIK3C2A 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087725 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Polyunsaturated omega-3 fatty acid levels (linolenic acid C18:3n3) 2,776 German ancestry individuals NA Affymetrix [577007] 0 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90012199 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Polyunsaturated omega-6 fatty acid levels (Arachidonic acid C20:4n6) 2,776 German ancestry individuals NA Affymetrix [577007] 0 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90012200 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Polyunsaturated omega-6 fatty acid levels (dihomo-g-linolenic acid C20:3n6) 2,776 German ancestry individuals NA Affymetrix [577007] 0 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90012201 Genome-wide genotyping array 2021-01-11 32915819 Zhou J 2020-09-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/32915819 Investigation of gene-gene interactions in cardiac traits and serum fatty acid levels in the LURIC Health Study. Polyunsaturated omega-3 fatty acid levels (EPA C20:5n3) 2,776 German ancestry individuals NA Affymetrix [577007] 0 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90012202 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGDCC3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086892 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGDCC3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089670 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGDCC4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090826 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGF1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088146 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGF1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090190 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGF1R 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088633 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGF2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089599 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGF2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089600 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGF2R 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088485 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFALS 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089525 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087652 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088062 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087961 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090210 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090319 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087962 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP4 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088145 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP5 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088017 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP6 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087772 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP6 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088018 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBP7 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088312 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFBPL1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089852 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFL1 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089387 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFL3 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089592 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFL4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089359 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIK3CA;PIK3R1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088357 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIK3CG 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088358 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIK3R1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090345 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PILRA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086458 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PILRA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089400 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PILRA 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090258 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PILRA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090260 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PILRA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090322 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIM1 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089021 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIN1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086214 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIN4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087183 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIP 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089271 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIP4K2A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087163 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIR 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087575 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PITPNA 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090920 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PITPNB 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087018 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PIWIL1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087230 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PKD2 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087472 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PKD2 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087656 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PKDCC 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090255 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PKLR 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086607 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PKM 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088637 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PKN1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087070 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PKP2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087755 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA1A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090732 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G10 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088144 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G12B 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090670 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G16 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089887 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G1B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088806 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G2A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088020 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G2C 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090338 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G2E 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087598 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G2E 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087943 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G5 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087944 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2G7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088872 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLA2R1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086499 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLAT 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087928 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IDE 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088262 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IDO1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090806 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IDS 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088263 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IDUA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088241 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IER3 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090822 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IER3IP1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089409 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFI16 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087295 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFI16 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087670 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFIT2 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090864 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFIT3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087579 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA10 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087805 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA10 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089178 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA14 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089711 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA16 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089417 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA17 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086275 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA2 5,324 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interferon alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020483 GCST90088420 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA4 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089773 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA5 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089297 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA6 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089162 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA7 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087806 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNA8 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089299 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNAR1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089270 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNAR1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090540 Genome-wide genotyping array 2022-06-07 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNB1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087804 Genome-wide genotyping array 2022-06-07 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNB1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089758 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNG 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90087817 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNG 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90088170 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNGR1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interferon gamma receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020484 GCST90089217 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNGR2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090318 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNGR2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090538 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNGR2 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090618 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNL1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087647 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNL1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088678 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNL2 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088679 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNL3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089161 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNLR1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089722 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IFNW1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089727 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGBP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086932 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDLIM4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086950 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDPK1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088698 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDRG1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087090 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDXK 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086536 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDXP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088575 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDZD11 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089301 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDZD7 5,317 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086952 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDZK1IP1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090087 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PEAR1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090099 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PEAR1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090365 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PEBP1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088648 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PECAM1 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088022 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PELI2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087168 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PELO 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086978 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PENK 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090491 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PES1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088645 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PEX14 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090113 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PEX14 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090248 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PEX5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089237 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PF4 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088024 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PF4V1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089132 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PFDN5 5,322 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088646 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PFKFB3 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086998 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PFN2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087351 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PGAM1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088574 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP2R1A 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087104 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP2R3A 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087594 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP2R5A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087567 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP3CA;PPP3R1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088799 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MBTPS1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089755 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCCD1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089998 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCEE 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090677 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCEMP1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089337 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCF2L 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087666 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCFD2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 8 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086292 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCL1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086238 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCL1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086253 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCM6 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090895 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MCTS1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087020 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MDH1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088547 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MDH2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087123 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MDK 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088129 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MDM1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089912 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MDM2 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 e3 ubiquitin-protein ligase mdm2 measurement http://www.ebi.ac.uk/efo/EFO_0020340 GCST90087398 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MDM2 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 e3 ubiquitin-protein ligase mdm2 measurement http://www.ebi.ac.uk/efo/EFO_0020340 GCST90088638 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MDM4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087399 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP3R1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088483 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP4R3A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086477 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPT1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090577 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPY 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088750 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PQBP1 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086742 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PQLC2L 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089937 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRB4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087088 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRC1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086812 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRCP 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089168 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRDM1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087831 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRDM4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087221 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MED1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089049 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MATN4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089650 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MEF2C 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090391 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAX 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086965 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAZ 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087442 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MB 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088201 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MBD1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087860 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MBD4 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088569 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MBL2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088178 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MICALL2 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087293 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MICB 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088924 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MICB 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090633 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MICU2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089305 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MICU3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089562 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MID2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087846 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MIF 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089018 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MIF 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090059 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MILR1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086587 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MINOS1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089948 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MINPP1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089076 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MIOX 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087483 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MLEC 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089339 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MLN 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089107 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MLYCD 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086782 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMEL1 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088466 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMGT1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089748 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088818 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP10 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086294 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP10 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088505 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP10 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090215 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP12 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088718 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP13 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088819 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP14 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088861 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP16 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088991 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP16 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090784 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP17 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088097 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP19 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089420 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088616 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP20 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089377 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088071 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DKK2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089488 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DKK3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90086433 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DKK3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90088455 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DKK4 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 Dickkopf-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008110 GCST90088345 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DKKL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 dickkopf-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020324 GCST90088477 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLD 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086191 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLG3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089911 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLG4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090029 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLK1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90089461 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLK1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90090168 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLK2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 toll-like receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020777 GCST90090654 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLL1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089011 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLL1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090091 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLL3 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090943 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLL4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088302 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLX3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086735 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DLX4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086881 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DMKN 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089249 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DMKN 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090226 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MET 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086865 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MET 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088096 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein METAP1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088272 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein METAP2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088242 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein METTL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087038 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein METTL24 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090707 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFAP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089088 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFAP2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090611 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFAP3L 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090330 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFAP4 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089112 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFAP5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089426 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFF 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086575 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFGE8 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088696 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFN1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086708 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFNG 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089087 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MFRP 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088488 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MGA 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086810 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MGAT1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086347 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MGAT2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089560 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MGAT4A 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090680 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MGAT4B 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089688 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MGAT4C 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089738 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MGP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089473 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MIA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088019 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MICA 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088036 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PNPLA2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090832 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PODXL2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086369 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POFUT1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089110 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POFUT2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089266 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POGLUT1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089446 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POLE2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086798 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POLH 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086188 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POLI 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087512 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POLM 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087269 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POLR1C 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087314 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POLR3F 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086750 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POMC 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087959 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POMC 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088796 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POMC 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090552 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POMGNT1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090081 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POMGNT2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089363 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POMK 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086353 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PON1 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088644 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POR 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088037 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POSTN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088398 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POSTN 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089455 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POSTN 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089544 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POSTN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089547 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POTEG 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089952 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POTEM 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089956 Genome-wide genotyping array 2021-10-11 33794208 Bowden SJ 2021-04-01 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/33794208 Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study. Cervical intraepithelial neoplasia grade 3 4,005 European ancestry cases, 145,545 European ancestry controls NA Affymetrix [9600464] (imputed) 2 Cervical Intraepithelial Neoplasia Grade 2/3 http://www.ebi.ac.uk/efo/EFO_1000166 GCST012476 Genome-wide genotyping array 2021-10-11 33794208 Bowden SJ 2021-04-01 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/33794208 Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study. Invasive cervical cancer 764 European ancestry cases, 145,545 European ancestry controls NA Affymetrix [9600464] (imputed) 2 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST012477 Genome-wide genotyping array 2021-10-11 33794208 Bowden SJ 2021-04-01 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/33794208 Genetic variation in cervical preinvasive and invasive disease: a genome-wide association study. Cervical intraepithelial neoplasia grade 3 and invasive cervical cancer 764 European ancestry invasive cervical cancer cases, 4,005 European ancestry cervical intraepithelial neoplasia grade 3 cases, 145,545 European ancestry controls NA Affymetrix [9600464] (imputed) 6 cervical carcinoma, Cervical Intraepithelial Neoplasia Grade 2/3 http://www.ebi.ac.uk/efo/EFO_0001061, http://www.ebi.ac.uk/efo/EFO_1000166 GCST012475 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MED1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088570 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRDX1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088549 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MATN3 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088270 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MED4 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087719 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MAVS 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090294 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MEGF10 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086584 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MEP1B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089597 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MEPE 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088271 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MESDC2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089080 Genome-wide genotyping array 2021-09-28 34482816 Xie C 2021-09-06 BMC Genom Data www.ncbi.nlm.nih.gov/pubmed/34482816 Genome-wide association study identifies new loci associated with noise-induced tinnitus in Chinese populations. Tinnitus in noise exposure 65 Chinese ancestry male cases, 233 Chinese ancestry male controls 34 Chinese ancestry male cases, 379 Chinese ancestry male controls Illumina [3830431] (imputed) 2 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90029167 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2J1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089557 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2J2 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089522 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2J2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090306 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2L3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088560 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2N 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088579 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2T 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086959 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2V1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086826 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE3A 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086622 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBL4A 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086768 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBQLN4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087184 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBTD2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087284 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBXN4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090941 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBXN4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090955 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UCHL1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088876 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UCK2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087039 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UCMA 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086524 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UCN3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086439 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UFC1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088368 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UFM1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088539 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UGP2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087669 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UGT1A6 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089906 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UGT1A8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090370 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UGT2A2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090376 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ULBP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087766 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ULBP1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088228 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNDC15 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089370 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNDC5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086613 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNIP 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086854 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNL4B 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087826 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNRD1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087687 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TYK2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088986 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TYMP 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086706 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TYMS 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088889 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TYMSOS 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090090 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TYRO3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087596 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TYRO3 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087978 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein U2AF2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087539 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UAP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087541 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBA2 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087028 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBASH3B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087068 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBB 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089542 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBB 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089548 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBC 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089294 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBC 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089545 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090872 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2C 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087066 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2D4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087464 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2E1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087866 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2G2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090549 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UBE2I 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088120 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TP53I11 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087339 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TP53I13 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089398 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TP63 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086198 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPI1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088659 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPK1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086905 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPM1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088887 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPM2 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088704 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPM3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086940 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPM3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090890 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPM4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089782 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPM4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090870 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPMT 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086617 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPO 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088559 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPPP2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087236 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPRKB 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086968 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPSB2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087910 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPSB2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088366 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPSB2;TPSAB1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090686 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPSG1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087785 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPSG1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088367 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPST1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089931 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPST2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089994 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPT1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087759 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TPT1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088558 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRA2B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086941 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRABD 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086645 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRABD2A 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090684 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRADD 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087491 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRAF4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086827 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRAF4 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087346 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRAPPC3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087871 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRAPPC4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089615 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRAPPC5 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090257 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRAT1 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089747 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRDMT1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087115 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREM1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090595 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREM2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086872 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREM2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086876 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREM2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089111 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREML1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086569 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREML1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090634 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREML2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089181 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TREML4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086562 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRH 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089129 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRIB2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086934 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRIL 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087786 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRIL 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089478 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRIM3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087077 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TRIO 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086554 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSG101 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087349 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ULBP2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088229 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ULBP3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088046 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ULK3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086983 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UMOD 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090697 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UMODL1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090516 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC13A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087745 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC45A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086862 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC45A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087362 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC5A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089960 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC5B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089824 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC5C 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 netrin receptor UNC5C measurement http://www.ebi.ac.uk/efo/EFO_0020590 GCST90088952 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC5D 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90088953 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC5D 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90090241 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UNC93B1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087473 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UPK3B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090103 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UPK3BL 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089540 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UQCC3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090062 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UQCRB 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087320 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UROS 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086638 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein USB1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086688 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein USE1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090018 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein USO1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087577 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein USP21 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087147 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein USP25 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090557 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein USP8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087448 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF1A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088007 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF1B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088238 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF1B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090159 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF21 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089029 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF21 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090590 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF25 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088902 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF4 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088499 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF6B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088900 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF8 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087975 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF9 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90087723 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFRSF9 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90087971 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF10 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090328 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF11 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087750 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF11 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088133 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF12 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089244 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF13B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088214 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF14 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089017 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF14 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089254 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF15 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087748 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF15 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088154 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF18 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088029 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087727 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088098 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF8 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088377 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNFSF9 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087972 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSLP 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088184 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087012 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSNARE1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089642 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSPEAR 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086331 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSR3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089624 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSSK1B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086592 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSSK2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089893 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TST 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 tuberculin skin test reactivity measurement http://www.ebi.ac.uk/efo/EFO_0008307 GCST90087135 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TSTA3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087130 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TTC1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090871 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TTC17 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090305 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TTC17 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090749 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TTC9B 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090675 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TTL 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087690 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TTN 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086699 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TUFT1 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089148 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TWF1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087281 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TWSG1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090571 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXLNA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090484 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXN 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086259 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXN 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090314 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNDC11 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086288 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNDC11 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090285 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNDC11 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090756 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TXNDC12 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088777 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNKS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090902 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNMD 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089509 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNNI2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089034 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNNI3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089035 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNNI3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089241 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNNT2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089000 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNR 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086673 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNRC6B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090835 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNS2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086846 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNS4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090913 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TNXB 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089154 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOLLIP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087685 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOM1L1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087584 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOMM20L 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086459 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOP1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088119 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOPBP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090927 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOR1AIP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086362 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOR1AIP1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090465 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOR1AIP2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086337 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOR1AIP2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086385 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOR4A 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087454 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TOX3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087182 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TP53 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089290 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TP53 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089292 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein TP53 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089293 Genome-wide genotyping array 2020-11-04 33097823 Pei YF 2020-10-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33097823 The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study. Appendicular lean mass 450,243 European ancestry individuals NA Affymetrix [18391927] (imputed) 1059 appendicular lean mass http://www.ebi.ac.uk/efo/EFO_0004980 GCST90000025 Genome-wide genotyping array 2020-11-04 33097823 Pei YF 2020-10-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33097823 The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study. Appendicular lean mass 205,513 European ancestry men NA Affymetrix [18391927] (imputed) 46 appendicular lean mass http://www.ebi.ac.uk/efo/EFO_0004980 GCST90000026 Genome-wide genotyping array 2020-11-04 33097823 Pei YF 2020-10-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33097823 The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study. Appendicular lean mass 244,730 European ancestry women NA Affymetrix [18391927] (imputed) 50 appendicular lean mass http://www.ebi.ac.uk/efo/EFO_0004980 GCST90000027 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. ADHD vs anorexia nervosa (ordinary least squares (OLS)) 19,099 ADHD cases, 16,992 anorexia nervosa cases NA NR [5496413] (imputed) 4 attention deficit hyperactivity disorder, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90016595 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. ADHD vs autism spectrum disorder (ordinary least squares (OLS)) 19,099 ADHD cases, 18,381 autism spectrum disorder cases NA NR [5798030] (imputed) 1 attention deficit hyperactivity disorder, autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003756 GCST90016596 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. ADHD vs obsessive compulsive disorder (ordinary least squares (OLS)) 19,099 ADHD cases, 2,688 OCD cases NA NR [5627061] (imputed) 2 obsessive-compulsive disorder, attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0003888 GCST90016597 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. ADHD vs Tourette's syndrome and other tic disorders (ordinary least squares (OLS)) 19,099 ADHD cases, 4,819 Tourette's syndrome cases NA NR [5616739] (imputed) 2 attention deficit hyperactivity disorder, Tourette syndrome http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004895 GCST90016598 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Anorexia nervosa vs autism spectrum disorder (ordinary least squares (OLS)) 16,992 anorexia nervosa cases, 18,381 autism spectrum disorder cases NA NR [5647804] (imputed) 1 autism spectrum disorder, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90016599 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Anorexia nervosa vs obsessive compulsive disorder (ordinary least squares (OLS)) 16,992 anorexia nervosa cases, 2,688 OCD cases NA NR [5520002] (imputed) 0 obsessive-compulsive disorder, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0004242, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90016600 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Anorexia nervosa vs Tourette's syndrome and other tic disorders (ordinary least squares (OLS)) 16,992 anorexia nervosa cases, 4,819 Tourette's syndrome cases NA NR [5508374] (imputed) 2 Tourette syndrome, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0004895, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90016601 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Autism spectrum disorder vs obsessive compulsive disorder (ordinary least squares (OLS)) 18,381 autism spectrum disorder cases, 2,688 OCD cases NA NR [6144458] (imputed) 1 obsessive-compulsive disorder, autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0003756 GCST90016602 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Autism spectrum disorder vs Tourette's syndrome and other tic disorders (ordinary least squares (OLS)) 18,381 autism spectrum disorder cases, 4,819 Tourette's syndrome cases NA NR [6126055] (imputed) 1 Tourette syndrome, autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0004895, http://www.ebi.ac.uk/efo/EFO_0003756 GCST90016603 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Bipolar disorder vs ADHD (ordinary least squares (OLS)) 20,352 bipolar disorder cases, 19,099 ADHD cases NA NR [5637374] (imputed) 8 attention deficit hyperactivity disorder, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0004985 GCST90016604 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Bipolar disorder vs anorexia nervosa (ordinary least squares (OLS)) 20,352 bipolar disorder cases, 16,992 anorexia nervosa cases NA NR [5569514] (imputed) 5 bipolar disorder, anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90016605 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Bipolar disorder vs autism spectrum disorder (ordinary least squares (OLS)) 20,352 bipolar disorder cases, 18,381 autism spectrum disorder cases NA NR [6135876] (imputed) 3 bipolar disorder, autism spectrum disorder http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756 GCST90016606 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Bipolar disorder vs major depressive disorder (ordinary least squares (OLS)) 20,352 bipolar disorder cases, 170,756 major depressive disorder cases NA NR [6265453] (imputed) 10 unipolar depression, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985 GCST90016607 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Bipolar disorder vs obsessive compulsive disorder (ordinary least squares (OLS)) 20,352 bipolar disorder cases, 2,688 OCD cases NA NR [6311569] (imputed) 1 obsessive-compulsive disorder, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0004242, http://purl.obolibrary.org/obo/MONDO_0004985 GCST90016608 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Bipolar disorder vs Tourette's syndrome and other tic disorders (ordinary least squares (OLS)) 20,352 bipolar disorder cases, 4,819 Tourette's syndrome cases NA NR [6254473] (imputed) 5 Tourette syndrome, bipolar disorder http://www.ebi.ac.uk/efo/EFO_0004895, http://purl.obolibrary.org/obo/MONDO_0004985 GCST90016609 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Crohn's disease vs rheumatoid arthritis (ordinary least squares (OLS)) 5,956 Crohn's disease cases, 8,875 rheumatoid arthritis cases 14,594 Crohn's disease cases, 5,486 rheumatoid arthritis cases NR [5890016] (imputed) 24 rheumatoid arthritis, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90016610 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Crohn's disease vs ulcerative colitis (ordinary least squares (OLS)) 5,956 Crohn's disease cases, 6,968 ulcerative colitis cases 14,594 Crohn's disease cases, 10,679 ulcerative colitis cases NR [6490614] (imputed) 8 ulcerative colitis, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000729, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90016611 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Major depressive disorder vs ADHD (ordinary least squares (OLS)) 170,756 MDD cases, 19,099 ADHD cases NA NR [5568121] (imputed) 9 attention deficit hyperactivity disorder, unipolar depression http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90016612 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Major depressive disorder vs anorexia nervosa (ordinary least squares (OLS)) 170,756 MDD cases, 16,992 anorexia nervosa cases NA NR [5460735] (imputed) 6 unipolar depression, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90016613 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Major depressive disorder vs autism spectrum disorder (ordinary least squares (OLS)) 170,756 MDD cases, 18,381 autism spectrum disorder cases NA NR [6057537] (imputed) 3 unipolar depression, autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0003756 GCST90016614 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Major depressive disorder vs obsessive compulsive disorder (ordinary least squares (OLS)) 170,756 MDD cases, 2,688 OCD cases NA NR [6207788] (imputed) 0 obsessive-compulsive disorder, unipolar depression http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90016615 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Major depressive disorder vs Tourette's syndrome and other tic disorders (ordinary least squares (OLS)) 170,756 MDD cases, 4,819 Tourette's syndrome cases NA NR [6202472] (imputed) 0 Tourette syndrome, unipolar depression http://www.ebi.ac.uk/efo/EFO_0004895, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90016616 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Obsessive compulsive disorder vs Tourette's syndrome and other tic disorders (ordinary least squares (OLS)) 2,688 OCD cases, 4,819 Tourette's syndrome cases NA NR [6349486] (imputed) 1 obsessive-compulsive disorder, Tourette syndrome http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0004895 GCST90016617 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Schizophrenia vs ADHD (ordinary least squares (OLS)) 40,675 schizophrenia cases, 19,099 ADHD cases NA NR [4428082] (imputed) 43 attention deficit hyperactivity disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90016618 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Schizophrenia vs anorexia nervosa (ordinary least squares (OLS)) 40,675 schizophrenia cases, 16,992 anorexia nervosa cases NA NR [4425810] (imputed) 41 schizophrenia, anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90016619 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Schizophrenia vs autism spectrum disorder (ordinary least squares (OLS)) 40,675 schizophrenia cases, 18,381 autism spectrum disorder cases NA NR [4484088] (imputed) 40 autism spectrum disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90016620 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Schizophrenia vs bipolar disorder (ordinary least squares (OLS)) 40,675 schizophrenia cases, 20,352 bipolar disorder cases NA NR [4548414] (imputed) 12 bipolar disorder, schizophrenia http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90016621 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Schizophrenia vs major depressive disorder (ordinary least squares (OLS)) 33,640 schizophrenia cases, 59,851 MDD cases 7,035 schizophrenia cases, 111,175 MDD cases NR [4483387] (imputed) 1 unipolar depression, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90016622 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Schizophrenia vs obsessive compulsive disorder (ordinary least squares (OLS)) 40,675 schizophrenia cases, 2,688 OCD cases NA NR [4503720] (imputed) 0 obsessive-compulsive disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0004242, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90016623 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Schizophrenia vs Tourette's syndrome and other tic disorders (ordinary least squares (OLS)) 40,675 schizophrenia cases, 4,819 Tourette's syndrome cases NA NR [4502103] (imputed) 13 Tourette syndrome, schizophrenia http://www.ebi.ac.uk/efo/EFO_0004895, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90016624 Genome-wide genotyping array 2021-04-27 33686288 Peyrot WJ 2021-03-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33686288 Identifying loci with different allele frequencies among cases of eight psychiatric disorders using CC-GWAS. Ulcerative colitis vs rheumatoid arthritis (ordinary least squares (OLS)) 6,968 ulcerative colitis cases, 8,875 rheumatoid arthritis cases 10,679 ulcerative colitis cases, 5,486 rheumatoid arthritis cases NR [5896510] (imputed) 15 rheumatoid arthritis, ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0000729 GCST90016625 Genome-wide genotyping array 2022-05-25 35568031 Sorokin EP 2022-05-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35568031 Analysis of MRI-derived spleen iron in the UK Biobank identifies genetic variation linked to iron homeostasis and hemolysis. Spleen iron concentration 35,324 European ancestry individuals NA NR [9390169] (imputed) 6 spleen iron measurement http://www.ebi.ac.uk/efo/EFO_0021421 GCST90101831 Genome-wide genotyping array 2021-09-02 33783297 Zai CC 2021-03-30 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/33783297 Genome-wide association study of suicidal behaviour severity in mood disorders. Suicide attempt severity in mood disorders 719 European ancestry bipolar disorder cases, 2,787 European ancestry major depressive disorder cases NA Illumina [6737359] (imputed) 17 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST012279 Genome-wide genotyping array 2021-09-02 33783297 Zai CC 2021-03-30 World J Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/33783297 Genome-wide association study of suicidal behaviour severity in mood disorders. Suicidality in mood disorders 719 European ancestry bipolar disorder cases, 2,787 European ancestry major depressive disorder cases NA Illumina [6737359] (imputed) 8 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST012280 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Asthma 445,865 European ancestry individuals NA Affymetrix [12007626] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90029018 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Menopause (age at onset) 156,364 European ancestry individuals NA Affymetrix [11991424] (imputed) 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90029037 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Morning person 452,896 European ancestry individuals NA Affymetrix [12007187] (imputed) 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90029029 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Neuroticism 393,411 European ancestry individuals NA Affymetrix [12003239] (imputed) 0 neurotic disorder http://www.ebi.ac.uk/efo/EFO_0004257 GCST90029028 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Number of children ever born 402,204 European ancestry individuals NA Affymetrix [12007269] (imputed) 0 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90029038 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Balding type 4 245,797 European ancestry individuals NA Affymetrix [11997003] (imputed) 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90029006 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Platelet distribution width 572,201 European ancestry individuals NA Affymetrix [12007224] (imputed) 0 platelet component distribution width http://www.ebi.ac.uk/efo/EFO_0007984 GCST90029000 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Body mass index 532,396 European ancestry individuals NA Affymetrix [12007571] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90029007 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Respiratory or ear-nose-throat disease 452,192 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 respiratory system disease, otorhinolaryngologic disease http://www.ebi.ac.uk/efo/EFO_0000684, http://purl.obolibrary.org/obo/MONDO_0024623 GCST90029023 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Dermatologic disease 459,279 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90029020 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Diastolic blood pressure 490,469 European ancestry individuals NA Affymetrix [12008250] (imputed) 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90029010 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Smoking status 468,170 European ancestry individuals NA Affymetrix [12007908] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90029014 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Educational attainment (years of education) 461,457 European ancestry individuals NA Affymetrix [12007096] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90029013 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Systolic blood pressure 469,767 European ancestry individuals NA Affymetrix [12008250] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90029011 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Tanning 513,536 European ancestry individuals NA Affymetrix [12007147] (imputed) 0 suntan http://www.ebi.ac.uk/efo/EFO_0004279 GCST90029035 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Hair color (dark brown) 531,771 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90029032 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Heel bone mineral density 583,314 European ancestry individuals NA Affymetrix [12006792] (imputed) 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90029004 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Height 673,878 European ancestry individuals NA Affymetrix [12007535] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90029008 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. High cholesterol 464,736 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90029021 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. High light scatter reticulocyte count 520,010 European ancestry individuals NA Affymetrix [12006910] (imputed) 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90028993 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Hypothyroidism 473,703 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90029022 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Lung function (FEV1/FVC) 446,811 European ancestry individuals NA Affymetrix [12005862] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90029026 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Lung function (FVC) 422,876 European ancestry individuals NA Affymetrix [12005862] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90029027 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. White blood cell count (monocyte) 545,193 European ancestry individuals NA Affymetrix [12007536] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90028998 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Menarche (age at onset) 279,470 European ancestry individuals NA Affymetrix [12006186] (imputed) 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90029036 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Autoimmune traits 469,184 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 autoimmune disease http://www.ebi.ac.uk/efo/EFO_0005140 GCST90029015 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Autoimmune traits 419,606 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 autoimmune disease http://www.ebi.ac.uk/efo/EFO_0005140 GCST90029016 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Balding type 1 247,331 European ancestry individuals NA Affymetrix [11997003] (imputed) 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90029005 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Platelet count 600,968 European ancestry individuals NA Affymetrix [12007558] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90028999 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Basal metabolic rate 534,045 European ancestry individuals NA Affymetrix [12007949] (imputed) 0 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST90029025 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Red blood cell count 526,540 European ancestry individuals NA Affymetrix [12007392] (imputed) 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90029002 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Red cell distribution width 514,929 European ancestry individuals NA Affymetrix [12007406] (imputed) 0 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90029001 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Cardiovascular disease 477,807 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90029019 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Skin pigmentation 548,203 European ancestry individuals NA Affymetrix [12006891] (imputed) 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90029033 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Educational attainment (college completion) 470,941 European ancestry individuals NA Affymetrix [12007096] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90029012 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Sunburns 350,232 European ancestry individuals NA Affymetrix [12010706] (imputed) 0 sunburn http://www.ebi.ac.uk/efo/EFO_0003958 GCST90029034 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Eczema 461,199 European ancestry individuals NA Affymetrix [12007626] (imputed) 0 Eczema http://purl.obolibrary.org/obo/HP_0000964 GCST90029017 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Hair color 713,771 European ancestry individuals NA Affymetrix [12008523] (imputed) 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90029030 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Hair color (blond) 534,365 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90029031 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Type 2 diabetes 468,298 European ancestry individuals NA Affymetrix [12007881] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90029024 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Waist-hip ratio 502,773 European ancestry individuals NA Affymetrix [12007603] (imputed) 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90029009 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. White blood cell count 503,190 European ancestry individuals NA Affymetrix [12007538] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90029003 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. White blood cell count (eosinophil) 513,859 European ancestry individuals NA Affymetrix [12007311] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90028992 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. White blood cell count (lymphocyte) 509,277 European ancestry individuals NA Affymetrix [12007506] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90028994 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Mean corpuscular hemoglobin 572,863 European ancestry individuals NA Affymetrix [12006845] (imputed) 0 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90028995 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Mean platelet volume 694,866 European ancestry individuals NA Affymetrix [12007520] (imputed) 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90028996 Genome-wide genotyping array 2021-09-24 29892013 Loh PR 2018-07-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29892013 Mixed-model association for biobank-scale datasets. Mean sphered cell volume 535,537 European ancestry individuals NA Affymetrix [12006744] (imputed) 0 hematological measurement http://www.ebi.ac.uk/efo/EFO_0004503 GCST90028997 Genome-wide genotyping array 2021-09-10 33762635 Martinez-Magana JJ 2021-03-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33762635 Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals. Risky substance use 1,165 Mexican ancestry cases, 1,487 Mexican ancestry controls NA Illumina [248101] 1 substance abuse http://purl.obolibrary.org/obo/MONDO_0002491 GCST90027269 Genome-wide genotyping array 2021-09-10 33762635 Martinez-Magana JJ 2021-03-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33762635 Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals. Psychiatric symptomatology 658 Mexican ancestry cases, 1,487 Mexican ancestry controls NA Illumina [248101] 8 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90027270 Genome-wide genotyping array 2021-09-10 33762635 Martinez-Magana JJ 2021-03-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33762635 Genome-wide association study of psychiatric and substance use comorbidity in Mexican individuals. Psychiatric symptomatology and risky substance use 604 Mexican ancestry cases, 1,487 Mexican ancestry controls NA Illumina [248101] 5 mental or behavioural disorder, substance abuse http://www.ebi.ac.uk/efo/EFO_0000677, http://purl.obolibrary.org/obo/MONDO_0002491 GCST90027271 Genome-wide genotyping array 2021-10-22 34340725 Campos AI 2021-08-03 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/34340725 Genetic Susceptibility to Pneumonia: A GWAS Meta-Analysis Between the UK Biobank and FinnGen. Pneumonia 24,760 European ancestry cases, 525,615 European ancestry controls NA NR [7831927] 20 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90027159 Genome-wide genotyping array 2022-05-20 35130970 Werdyani S 2022-02-07 Skelet Muscle www.ncbi.nlm.nih.gov/pubmed/35130970 Metabolomic signatures for the longitudinal reduction of muscle strength over 10 years. Asymmetrical dimethylarginine levels in osteoarthritis 77 individuals NA NR [NR] 2 asymmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006522 GCST90103750 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-12410 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095566 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-12112 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095570 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-methylpipecolate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095574 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Butyric acid levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095596 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-25435 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095605 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-21607 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095618 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Carotene diol (1) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095625 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Carotene diol (2) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095626 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-12411 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095634 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-24736 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095635 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-21851 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095639 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-21785 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095643 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 3-formylindole levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095644 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-22162 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095645 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Asparagine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90095612 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Glycine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90095502 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Orotate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 carboxylic acid anion measurement http://www.ebi.ac.uk/efo/EFO_0010467 GCST90095526 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Dimethylglycine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90095539 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 3-methylcytidine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90095527 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 2'-o-methyluridine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90095568 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 2'-o-methylcytidine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90095569 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Gamma-glutamylglycine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095504 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Fibrinopeptide A (2-15) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095540 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Fibrinopeptide A (3-15) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095541 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Glu-gly-asn-val levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095542 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetyl-1-methylhistidine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095518 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylarginine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095521 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylasparagine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095522 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylglutamine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095523 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-delta-acetylornithine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095524 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylcitrulline levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095525 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylglucosaminylasparagine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095548 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. S-1-pyrroline-5-carboxylate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095560 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 6-oxopiperidine-2-carboxylate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095561 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 4-acetamidobutanoate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095563 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetylputrescine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095567 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N6-methyllysine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095571 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N6,N6-dimethyllysine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095572 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N2-acetyl,N6,N6-dimethyllysine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095573 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N2-acetyl,N6-methyllysine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095575 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Dopamine 3-o-sulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095578 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-acetyl-aspartyl-glutamate (naag) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095579 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Methylsuccinate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095597 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Ethylmalonate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095600 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 1-methyl-4-imidazoleacetate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095611 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Dopamine 4-sulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095613 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5-hydroxylysine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095624 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Cys-gly, oxidized levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095627 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Cysteinylglycine disulfide levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095628 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N6-acetyllysine levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095630 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. N-formylanthranilic acid levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095631 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Glutaroylcarnitine (C5DC) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095633 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-18921 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095485 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-23680 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095486 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-24518 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095497 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-16570 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095503 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-16946 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095505 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Biliverdin levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095509 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Alliin levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095517 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-11787 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095519 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-23590 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095520 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Methyl glucopyranoside (alpha + beta) levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095528 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-23314 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095529 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-19141 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095530 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-24947 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095532 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-12117 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095535 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-24544 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095537 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-12798 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095547 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-13866 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095549 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-12822 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095551 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-11470 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095552 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. X-23659 levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095553 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. Metabolonic lactone sulfate levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095554 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5-acetylamino-6-amino-3-methyluracil levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095564 Genome-wide genotyping array 2022-03-22 34780722 Di Narzo AF 2021-11-12 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/34780722 Integrative analysis of the Inflammatory Bowel Disease serum metabolome improves our understanding of genetic etiology and points to novel putative therapeutic targets. 5-acetylamino-6-formylamino-3-methyluracil levels 712 European ancestry individuals NA Illumina [7008774] (imputed) 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90095565 Genome-wide genotyping array 2021-01-13 33414549 Demange PA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414549 Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction. Noncognitive aspects of educational attainment 510,795 European ancestry individuals NA Affymetrix, Illumina, Perlegen [7305956] (imputed) 151 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST90011874 Genome-wide genotyping array 2021-01-13 33414549 Demange PA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414549 Investigating the genetic architecture of noncognitive skills using GWAS-by-subtraction. Cognitive aspects of educational attainment 257,700 European ancestry individuals NA Affymetrix, Illumina, Perlegen [7305956] (imputed) 260 cognitive function measurement, self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0008354, http://www.ebi.ac.uk/efo/EFO_0004784 GCST90011875 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Anxiety 5,584 cases, 9,801 controls NA Affymetrix [NR] (imputed) 2 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST012450 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Depression 2,310 cases, 4,539 controls NA Affymetrix [NR] (imputed) 2 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST012445 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Depression x maternal smoking during pregnancy interaction 2,310 cases, 4,539 controls NA Affymetrix [NR] (imputed) 1 unipolar depression, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0005671 GCST012444 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Depression x maternal smoking during pregnancy interaction 2,310 cases, 4,539 controls NA Affymetrix [NR] (imputed) 3 unipolar depression, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0005671 GCST012443 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Anxiety 5,584 cases, 9,801 controls NA Affymetrix [NR] (imputed) 3 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST012449 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Anxiety x maternal smoking during pregnancy interaction 5,584 cases, 9,801 controls NA Affymetrix [NR] (imputed) 3 anxiety, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0005671 GCST012448 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Anxiety x maternal smoking during pregnancy interaction 5,584 cases, 9,801 controls NA Affymetrix [NR] (imputed) 3 anxiety, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0005671 GCST012447 Genome-wide genotyping array 2021-10-06 34118634 Chu X 2021-05-27 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/34118634 Maternal smoking during pregnancy and risks to depression and anxiety in offspring: An observational study and genome-wide gene-environment interaction analysis in UK biobank cohort. Depression 2,310 cases, 4,539 controls NA Affymetrix [NR] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST012446 Genome-wide genotyping array 2022-01-10 34611289 Escala-Garcia M 2021-10-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34611289 Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis. Breast cancer-specific survival 1,062 European ancestry individuals 293 European ancestry individuals NR [NR] (imputed) 0 survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90061436 Genome-wide genotyping array 2022-01-10 34611289 Escala-Garcia M 2021-10-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34611289 Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis. Breast cancer-specific survival (ER positive) 1,062 European ancestry individuals NA NR [NR] (imputed) 13 survival time, estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649 GCST90061437 Genome-wide genotyping array 2022-01-10 34611289 Escala-Garcia M 2021-10-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34611289 Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis. Breast cancer-specific survival (ER negative) 1,062 European ancestry individuals NA NR [NR] (imputed) 28 estrogen-receptor negative breast cancer, survival time http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000714 GCST90061438 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (basophil) 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90026520 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (eosinophil) 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90026521 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (lymphocyte) 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90026522 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (monocyte) 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90026523 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. White blood cell count (neutrophil) 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 3 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90026524 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Platelet count 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 20 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90026525 Genome-wide genotyping array 2021-10-26 34107879 Hu Y 2021-06-09 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/34107879 Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study. Mean platelet volume 27,236 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 9 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90026526 Genome-wide genotyping array 2021-11-12 33961016 Moksnes MR 2021-05-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33961016 Genome-wide association study of cardiac troponin I in the general population. Change in high-sensitivity cardiac troponin I concentration 5,178 European ancestry individuals NA Illumina [21233433] (imputed) 9 cardiac troponin I change measurement http://www.ebi.ac.uk/efo/EFO_0600077 GCST012500 Genome-wide genotyping array 2021-11-12 33961016 Moksnes MR 2021-05-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33961016 Genome-wide association study of cardiac troponin I in the general population. High-sensitivity cardiac troponin I concentration 48,115 European ancestry individuals NA Illumina [26711992] (imputed) 12 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST90054799 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming growth factor-beta-induced protein ig-h3 levels (TGFBI.3283.21.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transforming growth factor-beta-induced protein ig-h3 measurement http://www.ebi.ac.uk/efo/EFO_0008302 GCST90243062 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin-binding protein 1 levels (IGBP1.12358.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 immunoglobulin-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801691 GCST90241481 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Importin subunit alpha-1 levels (KPNA2.2860.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 importin subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020467 GCST90241482 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Importin subunit alpha-3 levels (KPNA4.12698.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 importin subunit alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0802623 GCST90241483 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inactive dipeptidyl peptidase 10 levels (DPP10.7890.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inactive dipeptidyl peptidase 10 measurement http://www.ebi.ac.uk/efo/EFO_0802624 GCST90241484 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inactive gamma-glutamyltranspeptidase 2 levels (GGT2.6334.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 inactive gamma-glutamyltranspeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801692 GCST90241485 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inactive pancreatic lipase-related protein 1 levels (PNLIPRP1.6627.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 inactive pancreatic lipase-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801693 GCST90241486 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inactive peptidyl-prolyl cis-trans isomerase FKBP6 levels (FKBP6.12529.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 inactive peptidyl-prolyl cis-trans isomerase FKBP6 measurement http://www.ebi.ac.uk/efo/EFO_0801694 GCST90241487 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inactive phospholipase D5 levels (PLD5.8081.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inactive phospholipase D5 measurement http://www.ebi.ac.uk/efo/EFO_0802625 GCST90241488 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inactive ribonuclease-like protein 10 levels (RNASE10.5602.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inactive ribonuclease-like protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0802626 GCST90241489 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Indoleamine 2,3-dioxygenase 1 levels (IDO1.9759.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 indoleamine 2,3-dioxygenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801695 GCST90241490 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Induced myeloid leukemia cell differentiation protein Mcl-1 levels (MCL1.10358.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 induced myeloid leukemia cell differentiation protein Mcl-1 measurement http://www.ebi.ac.uk/efo/EFO_0021910 GCST90241491 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inducible T-cell costimulator levels (ICOS.14084.191.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 inducible T-cell costimulator measurement http://www.ebi.ac.uk/efo/EFO_0021967 GCST90241492 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inducible T-cell costimulator levels (ICOS.2988.57.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inducible T-cell costimulator measurement http://www.ebi.ac.uk/efo/EFO_0021967 GCST90241493 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inhibin beta A chain levels (INHBA.2748.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inhibin beta A chain measurement http://www.ebi.ac.uk/efo/EFO_0020469 GCST90241494 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inhibin beta A chain levels (INHBA.INHBB.8467.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inhibin beta A chain measurement http://www.ebi.ac.uk/efo/EFO_0020469 GCST90241495 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inhibin beta A chain:Inhibin beta B chain heterodimer levels (INHBA.INHBB.4383.97.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inhibin beta A chain:inhibin beta B chain heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020470 GCST90241496 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inhibin beta C chain levels (INHBC.6408.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 inhibin beta C chain measurement http://www.ebi.ac.uk/efo/EFO_0801696 GCST90241497 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inhibitor of growth protein 1 levels (ING1.3888.8.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 inhibitor of growth protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020471 GCST90241498 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inosine-5'-monophosphate dehydrogenase 1 levels (IMPDH1.5229.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 inosine-5'-monophosphate dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008158 GCST90241499 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inosine-5'-monophosphate dehydrogenase 2 levels (IMPDH2.5250.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inosine-5'-monophosphate dehydrogenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008159 GCST90241500 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 levels (ITPRIPL1.9221.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801697 GCST90241501 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inositol monophosphatase 3 levels (IMPAD1.9231.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 inositol monophosphatase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801698 GCST90241502 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inositol polyphosphate 5-phosphatase OCRL-1 levels (OCRL.10011.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 inositol polyphosphate 5-phosphatase OCRL-1 measurement http://www.ebi.ac.uk/efo/EFO_0801699 GCST90241503 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inositol-trisphosphate 3-kinase A levels (ITPKA.13473.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 inositol-trisphosphate 3-kinase A measurement http://www.ebi.ac.uk/efo/EFO_0802627 GCST90241504 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell surface glycoprotein CD8 beta chain levels (CD8B.9310.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-cell surface glycoprotein CD8 beta chain measurement http://www.ebi.ac.uk/efo/EFO_0803135 GCST90242962 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell surface protein tactile levels (CD96.9735.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 T-cell surface protein tactile measurement http://www.ebi.ac.uk/efo/EFO_0802115 GCST90242963 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-lymphocyte activation antigen CD80 levels (CD80.2603.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-lymphocyte activation antigen CD80 measurement http://www.ebi.ac.uk/efo/EFO_0020761 GCST90242964 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-lymphocyte activation antigen CD86 levels (CD86.5337.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-lymphocyte activation antigen CD86 measurement http://www.ebi.ac.uk/efo/EFO_0020762 GCST90242965 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-lymphocyte surface antigen Ly-9 levels (LY9.3324.51.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 T-lymphocyte surface antigen Ly-9 measurement http://www.ebi.ac.uk/efo/EFO_0008295 GCST90242966 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. t-SNARE domain-containing protein 1 levels (TSNARE1.7069.9.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 t-SNARE domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802116 GCST90242967 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tachykinin-3 levels (TAC3.7847.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tachykinin-3 measurement http://www.ebi.ac.uk/efo/EFO_0803136 GCST90242968 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tachykinin-4 levels (TAC4.6468.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tachykinin-4 measurement http://www.ebi.ac.uk/efo/EFO_0803137 GCST90242969 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Talin-2 levels (TLN2.14082.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 talin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802117 GCST90242970 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tapasin levels (TAPBP.12378.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tapasin measurement http://www.ebi.ac.uk/efo/EFO_0802118 GCST90242971 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tapasin-related protein levels (TAPBPL.6364.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 tapasin-related protein measurement http://www.ebi.ac.uk/efo/EFO_0802119 GCST90242972 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tartrate-resistant acid phosphatase type 5 levels (ACP5.3232.28.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90242973 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. TATA-box-binding protein levels (TBP.2875.15.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tata-box-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020764 GCST90242974 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tax1-binding protein 1 levels (TAX1BP1.12721.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tax1-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803138 GCST90242975 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tax1-binding protein 3 levels (TAX1BP3.12498.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tax1-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802120 GCST90242976 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tenascin levels (TNC.4155.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90242977 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tenascin-R levels (TNR.11302.237.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tenascin-R measurement http://www.ebi.ac.uk/efo/EFO_0803139 GCST90242978 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tenascin-X levels (TNXB.5698.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 tenascin-X measurement http://www.ebi.ac.uk/efo/EFO_0802121 GCST90242979 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Teneurin-3 levels (TENM3.11107.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 teneurin-3 measurement http://www.ebi.ac.uk/efo/EFO_0803140 GCST90242980 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Teneurin-4 levels (TENM4.11365.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 teneurin-4 measurement http://www.ebi.ac.uk/efo/EFO_0803141 GCST90242981 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tenomodulin levels (TNMD.6578.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tenomodulin measurement http://www.ebi.ac.uk/efo/EFO_0803142 GCST90242982 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tensin-2 levels (TNS2.11667.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tensin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802122 GCST90242983 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tensin-4 levels (TNS4.9927.96.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tensin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802123 GCST90242984 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Teratocarcinoma-derived growth factor 1 levels (TDGF1.5810.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90242985 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testican-1 levels (SPOCK1.5490.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 testican-1 measurement http://www.ebi.ac.uk/efo/EFO_0020765 GCST90242986 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testican-2 levels (SPOCK2.5491.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 testican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020766 GCST90242987 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testican-3 levels (SPOCK3.9906.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 testican-3 measurement http://www.ebi.ac.uk/efo/EFO_0802124 GCST90242988 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testis-expressed sequence 29 protein levels (TEX29.10557.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 testis-expressed sequence 29 protein measurement http://www.ebi.ac.uk/efo/EFO_0802125 GCST90242989 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testis-expressed sequence 29 protein levels (TEX29.13500.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 testis-expressed sequence 29 protein measurement http://www.ebi.ac.uk/efo/EFO_0802125 GCST90242990 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testis-specific basic protein Y 1 levels (VCY.6295.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 testis-specific basic protein Y 1 measurement http://www.ebi.ac.uk/efo/EFO_0802126 GCST90242991 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testis-specific chromodomain protein Y 1 levels (CDY1.7097.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 testis-specific chromodomain protein Y 1 measurement http://www.ebi.ac.uk/efo/EFO_0802127 GCST90242992 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Testis-specific serine/threonine-protein kinase 2 levels (TSSK2.7873.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 testis-specific serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0803143 GCST90242993 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tetratricopeptide repeat protein 17 levels (TTC17.8800.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tetratricopeptide repeat protein 17 measurement http://www.ebi.ac.uk/efo/EFO_0803144 GCST90242994 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tetratricopeptide repeat protein 17 levels (TTC17.9550.153.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tetratricopeptide repeat protein 17 measurement http://www.ebi.ac.uk/efo/EFO_0803144 GCST90242995 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tetratricopeptide repeat protein 9B levels (TTC9B.9386.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tetratricopeptide repeat protein 9B measurement http://www.ebi.ac.uk/efo/EFO_0803145 GCST90242996 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. TGF-beta receptor type-2 levels (TGFBR2.5133.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tgf-beta receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020767 GCST90242997 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thiamin pyrophosphokinase 1 levels (TPK1.12018.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thiamin pyrophosphokinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803146 GCST90242998 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thioredoxin levels (TXN.8813.160.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thioredoxin measurement http://www.ebi.ac.uk/efo/EFO_0803148 GCST90242999 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thioredoxin domain-containing protein 11 levels (TXNDC11.8769.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thioredoxin domain-containing protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0803147 GCST90243000 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thioredoxin domain-containing protein 12 levels (TXNDC12.4815.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90243001 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thioredoxin domain-containing protein 5 levels (TXNDC5.11212.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 thioredoxin domain-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802128 GCST90243002 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thioredoxin reductase 1, cytoplasmic levels (TXNRD1.13967.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 thioredoxin reductase 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0802129 GCST90243003 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thioredoxin-interacting protein levels (TXNIP.11682.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thioredoxin-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0803149 GCST90243004 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thiosulfate sulfurtransferase levels (TST.12663.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 thiosulfate sulfurtransferase measurement http://www.ebi.ac.uk/efo/EFO_0802130 GCST90243005 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thrombopoietin levels (THPO.5947.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thrombopoietin measurement http://www.ebi.ac.uk/efo/EFO_0022004 GCST90243006 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thrombopoietin levels (THPO.8059.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thrombopoietin measurement http://www.ebi.ac.uk/efo/EFO_0022004 GCST90243007 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thrombopoietin Receptor levels (MPL.3473.78.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 thrombopoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020769 GCST90243008 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thrombospondin type-1 domain-containing protein 1 levels (THSD1.5621.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 thrombospondin type-1 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802131 GCST90243009 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thrombospondin type-1 domain-containing protein 7A levels (THSD7A.11174.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thrombospondin type-1 domain-containing protein 7A measurement http://www.ebi.ac.uk/efo/EFO_0803150 GCST90243010 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thrombospondin-2 levels (THBS2.3339.33.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90243011 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sushi domain-containing protein 1 levels (SUSD1.9582.93.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Sushi domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803111 GCST90242925 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sushi domain-containing protein 3 levels (SUSD3.5752.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Sushi domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803112 GCST90242927 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-11 levels (SYT11.7089.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 synaptotagmin-11 measurement http://www.ebi.ac.uk/efo/EFO_0802108 GCST90242935 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-2 levels (SYT2.9577.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptotagmin-2 measurement http://www.ebi.ac.uk/efo/EFO_0803118 GCST90242937 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-3 levels (SYT3.10452.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptotagmin-3 measurement http://www.ebi.ac.uk/efo/EFO_0803119 GCST90242938 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-5 levels (SYT5.9099.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptotagmin-5 measurement http://www.ebi.ac.uk/efo/EFO_0803120 GCST90242939 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-10 levels (STX10.12842.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 syntaxin-10 measurement http://www.ebi.ac.uk/efo/EFO_0802110 GCST90242944 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Haptoglobin levels (HP.3054.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90241371 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thrombospondin-3 levels (THBS3.8982.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thrombospondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0803151 GCST90243012 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thromboxane-A synthase levels (TBXAS1.8098.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thromboxane-A synthase measurement http://www.ebi.ac.uk/efo/EFO_0803152 GCST90243013 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thymic stromal lymphopoietin levels (TSLP.3010.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thymic stromal lymphopoietin measurement http://www.ebi.ac.uk/efo/EFO_0020772 GCST90243014 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thymidine kinase, cytosolic levels (TK1.4301.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thymidine kinase, cytosolic measurement http://www.ebi.ac.uk/efo/EFO_0020773 GCST90243015 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thymocyte nuclear protein 1 levels (THYN1.12424.107.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 thymocyte nuclear protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802132 GCST90243016 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thyroglobulin levels (TG.4165.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thyroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010050 GCST90243017 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thyroid hormone receptor alpha levels (THRA.12527.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thyroid hormone receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0803153 GCST90243018 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thyroid peroxidase levels (TPO.3873.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thyroid peroxidase measurement http://www.ebi.ac.uk/efo/EFO_0020775 GCST90243019 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Thyrotropin-releasing hormone levels (TRH.5659.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 thyrotropin-releasing hormone measurement http://www.ebi.ac.uk/efo/EFO_0803154 GCST90243020 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tight junction protein ZO-1 levels (TJP1.12001.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tight junction protein ZO-1 measurement http://www.ebi.ac.uk/efo/EFO_0803155 GCST90243021 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tissue Factor levels (F3.4931.59.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tissue factor measurement http://www.ebi.ac.uk/efo/EFO_0010623 GCST90243022 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tissue factor pathway inhibitor levels (TFPI.3336.50.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90243023 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tissue factor pathway inhibitor 2 levels (TFPI2.9233.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tissue factor pathway inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0803156 GCST90243024 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Titin levels (TTN.11352.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 titin measurement http://www.ebi.ac.uk/efo/EFO_0803157 GCST90243025 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. TNF receptor-associated factor 4 levels (TRAF4.13041.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 TNF receptor-associated factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0803158 GCST90243026 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Toll-interacting protein levels (TOLLIP.13963.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 toll-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0802133 GCST90243027 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Toll-like receptor 1 levels (TLR1.11149.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 toll-like receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0803159 GCST90243028 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Toll-like receptor 2 levels (TLR2.3835.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 toll-like receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020777 GCST90243029 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Toll-like receptor 4 levels (TLR4.11101.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 toll-like receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0021920 GCST90243030 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Toll-like receptor 4:Lymphocyte antigen 96 complex levels (TLR4.LY96.3647.49.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90243031 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Toll/interleukin-1 receptor domain-containing adapter protein levels (TIRAP.9839.148.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 toll/interleukin-1 receptor domain-containing adapter protein measurement http://www.ebi.ac.uk/efo/EFO_0802134 GCST90243032 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tolloid-like protein 1 levels (TLL1.6383.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tolloid-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802135 GCST90243033 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. TOM1-like protein 1 levels (TOM1L1.13652.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 TOM1-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802136 GCST90243034 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Torsin-1A-interacting protein 1 levels (TOR1AIP1.9039.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 torsin-1A-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802137 GCST90243035 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Torsin-1A-interacting protein 2 levels (TOR1AIP2.10640.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 torsin-1A-interacting protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803160 GCST90243036 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Torsin-1A-interacting protein 2 levels (TOR1AIP2.10553.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 torsin-1A-interacting protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803160 GCST90243037 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. TOX high mobility group box family member 3 levels (TOX3.12717.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 TOX high mobility group box family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0803161 GCST90243038 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. TPA-induced transmembrane protein levels (TTMP.7963.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 TPA-induced transmembrane protein measurement http://www.ebi.ac.uk/efo/EFO_0803162 GCST90243039 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcobalamin-1 levels (TCN1.11232.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 transcobalamin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802138 GCST90243040 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcobalamin-2 levels (TCN2.5584.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 transcobalamin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802139 GCST90243041 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcription factor AP-1 levels (JUN.10356.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcription factor AP-1 measurement http://www.ebi.ac.uk/efo/EFO_0021909 GCST90243042 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcription factor IIIB 90 kDa subunit levels (BRF1.5384.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcription factor IIIb 90 kda subunit measurement http://www.ebi.ac.uk/efo/EFO_0020778 GCST90243043 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcription factor RelB levels (RELB.11464.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transcription factor RelB measurement http://www.ebi.ac.uk/efo/EFO_0802140 GCST90243044 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcription factor TFIIIB component B'' homolog levels (BDP1.8929.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcription factor TFIIIB component B'' homolog measurement http://www.ebi.ac.uk/efo/EFO_0803163 GCST90243045 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcription regulator protein BACH1 levels (BACH1.12451.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transcription regulator protein BACH1 measurement http://www.ebi.ac.uk/efo/EFO_0802141 GCST90243046 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcription regulator protein BACH2 levels (BACH2.12756.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcription regulator protein BACH2 measurement http://www.ebi.ac.uk/efo/EFO_0803164 GCST90243047 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcriptional activator protein Pur-alpha levels (PURA.12537.88.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcriptional activator protein Pur-alpha measurement http://www.ebi.ac.uk/efo/EFO_0803165 GCST90243048 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcriptional enhancer factor TEF-3 levels (TEAD4.12516.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcriptional enhancer factor TEF-3 measurement http://www.ebi.ac.uk/efo/EFO_0803166 GCST90243049 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcriptional enhancer factor TEF-5 levels (TEAD3.12854.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcriptional enhancer factor TEF-5 measurement http://www.ebi.ac.uk/efo/EFO_0803167 GCST90243050 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcriptional regulator Kaiso levels (ZBTB33.12785.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcriptional regulator Kaiso measurement http://www.ebi.ac.uk/efo/EFO_0803168 GCST90243051 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transcriptional repressor CTCF levels (CTCF.14624.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transcriptional repressor CTCF measurement http://www.ebi.ac.uk/efo/EFO_0803169 GCST90243052 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transferrin receptor protein 1 levels (TFRC.8795.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transferrin receptor protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802142 GCST90243053 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transferrin receptor protein 1 levels (TFRC.6895.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transferrin receptor protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802142 GCST90243054 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transformer-2 protein homolog beta levels (TRA2B.12373.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transformer-2 protein homolog beta measurement http://www.ebi.ac.uk/efo/EFO_0802143 GCST90243055 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming growth factor alpha levels (TGFA.9358.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transforming growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0010798 GCST90243056 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming growth factor beta receptor type 3 levels (TGFBR3.3009.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transforming growth factor beta receptor type 3 measurement http://www.ebi.ac.uk/efo/EFO_0020779 GCST90243057 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming growth factor beta-1 levels (TGFB1.2333.72.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transforming growth factor beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020780 GCST90243058 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming growth factor beta-1-induced transcript 1 protein levels (TGFB1I1.8777.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transforming growth factor beta-1-induced transcript 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0803170 GCST90243059 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming growth factor beta-2 levels (TGFB2.4156.74.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transforming growth factor beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020781 GCST90243060 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming growth factor beta-3 levels (TGFB3.3520.58.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transforming growth factor beta-3 measurement http://www.ebi.ac.uk/efo/EFO_0020782 GCST90243061 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin levels (INS.4883.56.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90241505 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin gene enhancer protein ISL-1 levels (ISL1.11549.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin gene enhancer protein ISL-1 measurement http://www.ebi.ac.uk/efo/EFO_0802628 GCST90241506 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin growth factor-like family member 3 levels (IGFL3.6961.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 insulin growth factor-like family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0801700 GCST90241507 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin growth factor-like family member 4 levels (IGFL4.6353.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 insulin growth factor-like family member 4 measurement http://www.ebi.ac.uk/efo/EFO_0801701 GCST90241508 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin receptor levels (INSR.3448.13.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 insulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008160 GCST90241509 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-degrading enzyme levels (IDE.3197.70.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-degrading enzyme measurement http://www.ebi.ac.uk/efo/EFO_0020472 GCST90241510 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-induced gene 1 protein levels (INSIG1.10663.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-induced gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802629 GCST90241511 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like 3 levels (INSL3.5723.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like 3 measurement http://www.ebi.ac.uk/efo/EFO_0802630 GCST90241512 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor 1 receptor levels (IGF1R.4232.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 insulin-like growth factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020473 GCST90241513 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor I levels (IGF1.2952.75.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 insulin-like growth factor I measurement http://www.ebi.ac.uk/efo/EFO_0801702 GCST90241514 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor-binding protein 1 levels (IGFBP1.13741.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90241515 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor-binding protein 1 levels (IGFBP1.2771.35.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90241516 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor-binding protein 2 levels (IGFBP2.2570.72.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90241517 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor-binding protein 3 levels (IGFBP3.2571.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 insulin-like growth factor-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801703 GCST90241518 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor-binding protein 6 levels (IGFBP6.14088.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like growth factor-binding protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020478 GCST90241519 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor-binding protein 7 levels (IGFBP7.3320.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90241520 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like growth factor-binding protein-like 1 levels (IGFBPL1.7815.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like growth factor-binding protein-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0802631 GCST90241521 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like peptide INSL5 levels (INSL5.10462.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like peptide INSL5 measurement http://www.ebi.ac.uk/efo/EFO_0802632 GCST90241522 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Insulin-like peptide INSL6 levels (INSL6.5754.76.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 insulin-like peptide INSL6 measurement http://www.ebi.ac.uk/efo/EFO_0802633 GCST90241523 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integral membrane protein 2A levels (ITM2A.7765.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 integral membrane protein 2A measurement http://www.ebi.ac.uk/efo/EFO_0801704 GCST90241524 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integral membrane protein 2A levels (ITM2A.10516.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integral membrane protein 2A measurement http://www.ebi.ac.uk/efo/EFO_0801704 GCST90241525 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integral membrane protein 2B levels (ITM2B.8086.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integral membrane protein 2B measurement http://www.ebi.ac.uk/efo/EFO_0802634 GCST90241526 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integral membrane protein 2C levels (ITM2C.10560.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integral membrane protein 2C measurement http://www.ebi.ac.uk/efo/EFO_0802635 GCST90241527 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integral membrane protein 2C levels (ITM2C.9523.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integral membrane protein 2C measurement http://www.ebi.ac.uk/efo/EFO_0802635 GCST90241528 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integral membrane protein DGCR2/IDD levels (DGCR2.8055.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integral membrane protein DGCR2/IDD measurement http://www.ebi.ac.uk/efo/EFO_0802636 GCST90241529 Genome-wide genotyping array 2021-12-07 30002152 Jian X 2018-08-01 Stroke www.ncbi.nlm.nih.gov/pubmed/30002152 Exome Chip Analysis Identifies Low-Frequency and Rare Variants in MRPL38 for White Matter Hyperintensities on Brain Magnetic Resonance Imaging. White matter hyperintensities 7, 790 European ancestry individuals, 2,929 African American individuals 1,192 European ancestry individuals Illumina [Exome array] 9 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST012580 Exome genotyping array [Exome array] 2022-01-10 34684477 Fujihara K 2021-09-30 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684477 Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. body mass index x carrot consumption interaction 6,495 Japanese ancestry males, 5,730 Japanese ancestry females NA Illumina [285387] 3 diet measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090968 Genome-wide genotyping array 2022-01-10 34684477 Fujihara K 2021-09-30 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684477 Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. body mass index x broccoli consumption interaction 6,495 Japanese ancestry males, 5,730 Japanese ancestry females NA Illumina [285387] 2 diet measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090969 Genome-wide genotyping array 2022-01-10 34684477 Fujihara K 2021-09-30 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684477 Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. body mass index x spinach consumption interaction 6,495 Japanese ancestry males, 5,730 Japanese ancestry females NA Illumina [285387] 0 diet measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090970 Genome-wide genotyping array 2022-01-10 34684477 Fujihara K 2021-09-30 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684477 Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. body mass index x other green vegetables (green pepper and green beans) consumption interaction 6,495 Japanese ancestry males, 5,730 Japanese ancestry females NA Illumina [285387] 2 diet measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090971 Genome-wide genotyping array 2022-01-10 34684477 Fujihara K 2021-09-30 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684477 Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. body mass index x pumpkin consumption interaction 6,495 Japanese ancestry males, 5,730 Japanese ancestry females NA Illumina [285387] 2 diet measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090972 Genome-wide genotyping array 2022-01-10 34684477 Fujihara K 2021-09-30 Nutrients www.ncbi.nlm.nih.gov/pubmed/34684477 Carrot Consumption Frequency Associated with Reduced BMI and Obesity through the SNP Intermediary rs4445711. body mass index x cabbage consumption interaction 6,495 Japanese ancestry males, 5,730 Japanese ancestry females NA Illumina [285387] 1 diet measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90090973 Genome-wide genotyping array 2022-02-16 34834452 Pisanu C 2021-10-27 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834452 Investigating the Role of Leukocyte Telomere Length in Treatment-Resistant Depression and in Response to Electroconvulsive Therapy. Leukocyte telomere length in electroconvulsive therapy treatment-resistant depression 107 individuals NA Illumina [NR] (imputed) 0 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST012757 Genome-wide genotyping array 2022-02-16 34834452 Pisanu C 2021-10-27 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834452 Investigating the Role of Leukocyte Telomere Length in Treatment-Resistant Depression and in Response to Electroconvulsive Therapy. Response to electroconvulsive therapy in depression 107 individuals NA Illumina [NR] (imputed) 0 treatment outcome measurement http://www.ebi.ac.uk/efo/EFO_0008383 GCST012756 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tartronate (hydroxymalonate) levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134242 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Xanthosine levels in elite athletes 490 individuals NA Illumina [275016] 7 xanthosine measurement http://www.ebi.ac.uk/efo/EFO_0010549 GCST90134243 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Xanthurenate levels in elite athletes 490 individuals NA Illumina [275016] 4 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90134244 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Thioproline levels in elite athletes 490 individuals NA Illumina [275016] 7 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134245 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Umbelliferone sulfate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134246 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-GPE (P-16:0) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133662 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Methionine sulfone levels in elite athletes 490 individuals NA Illumina [275016] 10 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133569 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Methylsuccinate levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133570 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetyl-1-methylhistidine levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133571 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetyl-3-methylhistidine levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133572 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetyl-aspartyl-glutamate (NAAG) levels in elite athletes 490 individuals NA Illumina [275016] 19 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133573 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetyl-cadaverine levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133574 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylalanine levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133575 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylasparagine levels in elite athletes 490 individuals NA Illumina [275016] 8 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133576 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylaspartate (NAA) levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133577 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylcitrulline levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133578 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylglutamate levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133579 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylglutamine levels in elite athletes 490 individuals NA Illumina [275016] 7 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133580 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylisoleucine levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133581 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylkynurenine (2) levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133582 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylleucine levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133583 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylmethionine sulfoxide levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133584 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylphenylalanine levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133585 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylproline levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133586 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylputrescine levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133587 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylserine levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133588 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylthreonine levels in elite athletes 490 individuals NA Illumina [275016] 1 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133589 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetyltryptophan levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133590 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylvaline levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133591 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-alpha-acetylornithine levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133592 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-delta-acetylornithine levels in elite athletes 490 individuals NA Illumina [275016] 11 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133593 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-formylanthranilic acid levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133594 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-formylmethionine levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133595 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-formylphenylalanine levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133596 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-methylproline levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133597 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-trimethyl 5-aminovalerate levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133598 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N2-acetyllysine levels in elite athletes 490 individuals NA Illumina [275016] 9 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133599 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N2,N5-diacetylornithine levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133600 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N6-acetyllysine levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133601 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N6,N6,N6-trimethyllysine levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133602 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. S-1-pyrroline-5-carboxylate levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133603 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. S-methylcysteine sulfoxide levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133604 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. S-methylcysteine levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133605 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. S-methylmethionine levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133606 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,3,7-trimethylurate levels in elite athletes 490 individuals NA Illumina [275016] 5 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90133607 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,5-anhydroglucitol (1,5-AG) levels in elite athletes 490 individuals NA Illumina [275016] 4 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90133608 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,7-dimethylurate levels in elite athletes 490 individuals NA Illumina [275016] 5 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90133609 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Spermidine levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133610 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 10-nonadecenoate (19:1n9) levels in elite athletes 490 individuals NA Illumina [275016] 1 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90133611 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tiglylcarnitine (C5:1-DC) levels in elite athletes 490 individuals NA Illumina [275016] 10 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133612 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Xylella) 99 Chinese ancestry cases, 519 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094162 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Bordetella) 96 Chinese ancestry cases, 522 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094163 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Stenotrophomonas) 94 Chinese ancestry cases, 524 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094164 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Cardiobacterium) 92 Chinese ancestry cases, 526 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094165 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Macrococcus) 91 Chinese ancestry cases, 527 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094166 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Anaeromyxobacter) 88 Chinese ancestry cases, 530 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094167 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Desulfobulbus) 88 Chinese ancestry cases, 530 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094168 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Mannheimia) 86 Chinese ancestry cases, 532 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094169 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Erysipelothrix) 82 Chinese ancestry cases, 536 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094170 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thermincola) 81 Chinese ancestry cases, 537 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094171 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Sphingopyxis) 79 Chinese ancestry cases, 539 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094172 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Syntrophobacter) 79 Chinese ancestry cases, 539 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094173 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Jonquetella) 75 Chinese ancestry cases, 543 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094174 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Natranaerobius) 73 Chinese ancestry cases, 545 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094175 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Dehalogenimonas) 69 Chinese ancestry cases, 549 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094176 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Leptospira) 69 Chinese ancestry cases, 549 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094177 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Rhodospirillum) 68 Chinese ancestry cases, 550 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094178 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Desulfuromonas) 68 Chinese ancestry cases, 550 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094179 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Methyloversatilis) 66 Chinese ancestry cases, 552 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094180 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Geobacillus) 65 Chinese ancestry cases, 553 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094181 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Magnetococcus) 64 Chinese ancestry cases, 554 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094182 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Variovorax) 64 Chinese ancestry cases, 554 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094183 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Oceanithermus) 62 Chinese ancestry cases, 556 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094184 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_salivarius) 585 Chinese ancestry cases, 33 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094185 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Fusobacterium_mortiferum) 582 Chinese ancestry cases, 36 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094186 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_infantarius) 579 Chinese ancestry cases, 39 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094187 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Anaerococcus_vaginalis) 578 Chinese ancestry cases, 40 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094188 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Atopobium_parvulum) 577 Chinese ancestry cases, 41 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094189 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Weissella_cibaria) 577 Chinese ancestry cases, 41 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094190 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Peptoniphilus_lacrimalis) 575 Chinese ancestry cases, 43 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094191 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Collinsella_intestinalis) 571 Chinese ancestry cases, 47 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094192 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Clostridium_sp__7_2_43FAA) 571 Chinese ancestry cases, 47 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094193 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_bergensis) 570 Chinese ancestry cases, 48 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094194 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Providencia_rettgeri) 570 Chinese ancestry cases, 48 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094195 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Actinomyces_odontolyticus) 568 Chinese ancestry cases, 50 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094196 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Bacteroides_coprosuis) 565 Chinese ancestry cases, 53 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094197 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Treponema_denticola) 565 Chinese ancestry cases, 53 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094198 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Peptostreptococcus_stomatis) 564 Chinese ancestry cases, 54 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094199 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Victivallis_vadensis) 562 Chinese ancestry cases, 56 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094200 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Bifidobacterium_angulatum) 559 Chinese ancestry cases, 59 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094201 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Citrobacter_youngae) 558 Chinese ancestry cases, 60 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094202 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Proteus_mirabilis) 548 Chinese ancestry cases, 70 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094203 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Peptoniphilus_harei) 546 Chinese ancestry cases, 72 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094204 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Ruminococcus_flavefaciens) 543 Chinese ancestry cases, 75 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094205 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Desulfovibrio_sp__3_1_syn3) 541 Chinese ancestry cases, 77 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094206 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Parvimonas_micra) 541 Chinese ancestry cases, 77 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094207 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Turicibacter_sanguinis) 541 Chinese ancestry cases, 77 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094208 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Campylobacter_concisus) 541 Chinese ancestry cases, 77 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094209 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Bifidobacterium_dentium) 540 Chinese ancestry cases, 78 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094210 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Fusobacterium_varium) 537 Chinese ancestry cases, 81 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094211 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lawsonia_intracellularis) 535 Chinese ancestry cases, 83 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094212 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Acidaminococcus_intestini) 535 Chinese ancestry cases, 83 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094213 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_denticola) 533 Chinese ancestry cases, 85 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094214 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Abiotrophia_defectiva) 531 Chinese ancestry cases, 87 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094215 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_amylovorus) 531 Chinese ancestry cases, 87 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094216 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_dentalis) 524 Chinese ancestry cases, 94 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094217 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Aggregatibacter_aphrophilus) 517 Chinese ancestry cases, 101 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094218 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_gasseri) 512 Chinese ancestry cases, 106 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094219 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_melaninogenica) 504 Chinese ancestry cases, 114 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094220 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_fermentum) 502 Chinese ancestry cases, 116 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094221 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_pallens) 493 Chinese ancestry cases, 125 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094222 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_delbrueckii) 486 Chinese ancestry cases, 132 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094223 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_casei) 483 Chinese ancestry cases, 135 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094224 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Vibrio_cholerae) 481 Chinese ancestry cases, 137 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094225 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Atopobium_vaginae) 479 Chinese ancestry cases, 139 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094226 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Acinetobacter_baumannii) 478 Chinese ancestry cases, 140 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094227 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Oribacterium_sp__oral_taxon_108) 478 Chinese ancestry cases, 140 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094228 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Pseudomonas_stutzeri) 473 Chinese ancestry cases, 145 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094229 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Staphylococcus_aureus) 471 Chinese ancestry cases, 147 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094230 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Streptococcus_oralis) 470 Chinese ancestry cases, 148 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094231 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridiales_genomosp__BVAB3) 466 Chinese ancestry cases, 152 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094232 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Porphyromonas_gingivalis) 465 Chinese ancestry cases, 153 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094233 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Fusobacterium_ulcerans) 464 Chinese ancestry cases, 154 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094234 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Collinsella_stercoris) 457 Chinese ancestry cases, 161 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094235 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridium_kluyveri) 456 Chinese ancestry cases, 162 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094236 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Eubacterium_cellulosolvens) 306 Chinese ancestry cases, 312 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094287 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Pantoea_ananatis) 304 Chinese ancestry cases, 314 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094288 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Fusobacterium_gonidiaformans) 304 Chinese ancestry cases, 314 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094289 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Oscillibacter_valericigenes) 298 Chinese ancestry cases, 320 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094290 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_reuteri) 297 Chinese ancestry cases, 321 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094291 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_sicca/macacae) 293 Chinese ancestry cases, 325 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094292 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Selenomonas_artemidis) 291 Chinese ancestry cases, 327 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094293 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Comamonas_testosteroni) 287 Chinese ancestry cases, 331 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094294 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_peroris) 286 Chinese ancestry cases, 332 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094295 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_pseudopneumoniae) 283 Chinese ancestry cases, 335 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094296 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Prevotella_sp__oral_taxon_472) 276 Chinese ancestry cases, 342 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094297 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Thermoanaerobacter_pseudethanolicus) 274 Chinese ancestry cases, 344 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094298 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Achromobacter_piechaudii) 272 Chinese ancestry cases, 346 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094299 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridium_butyricum) 271 Chinese ancestry cases, 347 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094300 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Desulfovibrio_alaskensis) 268 Chinese ancestry cases, 350 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094301 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Brucella_melitensis) 267 Chinese ancestry cases, 351 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094302 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_meningitidis) 267 Chinese ancestry cases, 351 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094303 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Enterococcus_gallinarum) 265 Chinese ancestry cases, 353 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094304 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Fusobacterium_sp__D12) 260 Chinese ancestry cases, 358 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094305 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Bacillus_anthracis/cereus/thuringiensis) 258 Chinese ancestry cases, 360 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094306 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Yersinia_pseudotuberculosis) 256 Chinese ancestry cases, 362 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094307 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Shewanella_frigidimarina) 253 Chinese ancestry cases, 365 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094308 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Mobiluncus_mulieris) 249 Chinese ancestry cases, 369 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094309 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Peptoniphilus_sp__oral_taxon_386) 249 Chinese ancestry cases, 369 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094310 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Shuttleworthia_satelles) 248 Chinese ancestry cases, 370 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094311 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_casei_group) 245 Chinese ancestry cases, 373 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094312 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Enterobacter_sp__638) 245 Chinese ancestry cases, 373 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094313 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Eubacterium_saphenum) 243 Chinese ancestry cases, 375 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094314 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Sodalis_glossinidius) 242 Chinese ancestry cases, 376 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094315 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_acidophilus) 239 Chinese ancestry cases, 379 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094316 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Methylobacillus_flagellatus) 238 Chinese ancestry cases, 380 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094317 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Aggregatibacter_actinomycetemcomitans) 236 Chinese ancestry cases, 382 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094318 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Plautia_stali_symbiont) 231 Chinese ancestry cases, 387 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094319 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Aeromonas_veronii) 225 Chinese ancestry cases, 393 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094320 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Kingella_denitrificans) 224 Chinese ancestry cases, 394 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094321 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Salmonella_bongori) 216 Chinese ancestry cases, 402 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094322 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_cinerea) 212 Chinese ancestry cases, 406 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094323 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Ethanoligenens_harbinense) 207 Chinese ancestry cases, 411 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094324 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_salivae) 200 Chinese ancestry cases, 418 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094325 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Desulfovibrio_aespoeensis) 198 Chinese ancestry cases, 420 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094326 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Methanobrevibacter_smithii) 193 Chinese ancestry cases, 425 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094327 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Cronobacter_sakazakii/turicensis) 189 Chinese ancestry cases, 429 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094328 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Acinetobacter_johnsonii) 187 Chinese ancestry cases, 431 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094329 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Desulfovibrio_desulfuricans) 185 Chinese ancestry cases, 433 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094330 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_oris) 182 Chinese ancestry cases, 436 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094331 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Histophilus_somni) 180 Chinese ancestry cases, 438 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094332 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_agalactiae) 177 Chinese ancestry cases, 441 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094333 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Actinobacillus_pleuropneumoniae) 177 Chinese ancestry cases, 441 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094334 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Gemella_morbillorum) 173 Chinese ancestry cases, 445 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094335 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Erwinia_amylovora) 173 Chinese ancestry cases, 445 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094336 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_flavescens) 376 Chinese ancestry cases, 242 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094262 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Pyramidobacter_piscolens) 375 Chinese ancestry cases, 243 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094263 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Streptococcus_sp__M143) 375 Chinese ancestry cases, 243 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094264 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Porphyromonas_uenonis) 371 Chinese ancestry cases, 247 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094265 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Enterobacter_cancerogenus) 368 Chinese ancestry cases, 250 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094266 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Citrobacter_rodentium) 363 Chinese ancestry cases, 255 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094267 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_multiformis) 361 Chinese ancestry cases, 257 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094268 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_vaginalis) 351 Chinese ancestry cases, 267 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094269 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_marshii) 351 Chinese ancestry cases, 267 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094270 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Fusobacterium_periodonticum) 348 Chinese ancestry cases, 270 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094271 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Corynebacterium_glucuronolyticum) 345 Chinese ancestry cases, 273 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094272 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Thauera_sp__MZ1T) 341 Chinese ancestry cases, 277 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094273 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence ([Clostridium]_hiranonis) 339 Chinese ancestry cases, 279 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094274 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Peptoniphilus_duerdenii) 338 Chinese ancestry cases, 280 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094275 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Finegoldia_magna) 336 Chinese ancestry cases, 282 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094276 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Porphyromonas_endodontalis) 332 Chinese ancestry cases, 286 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094277 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_crispatus) 329 Chinese ancestry cases, 289 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094278 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_veroralis) 328 Chinese ancestry cases, 290 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094279 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridium_phytofermentans) 327 Chinese ancestry cases, 291 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094280 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Slackia_exigua) 325 Chinese ancestry cases, 293 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094281 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Acinetobacter_haemolyticus) 322 Chinese ancestry cases, 296 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094282 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_constellatus) 318 Chinese ancestry cases, 300 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094283 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Rahnella_aquatilis) 312 Chinese ancestry cases, 306 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094284 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Succinatimonas_hippei) 310 Chinese ancestry cases, 308 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094285 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Eggerthella_sp__YY7918) 308 Chinese ancestry cases, 310 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094286 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Delftia) 184 Chinese ancestry cases, 434 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094137 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Dehalococcoides) 180 Chinese ancestry cases, 438 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094138 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Xenorhabdus) 175 Chinese ancestry cases, 443 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094139 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thioalkalivibrio) 168 Chinese ancestry cases, 450 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094140 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Rothia) 163 Chinese ancestry cases, 455 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094141 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thiomonas) 163 Chinese ancestry cases, 455 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094142 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Coriobacterium) 148 Chinese ancestry cases, 470 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094143 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Nitrosococcus) 147 Chinese ancestry cases, 471 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094144 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Parascardovia) 143 Chinese ancestry cases, 475 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094145 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Azospira) 141 Chinese ancestry cases, 477 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094146 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Actinoplanes) 128 Chinese ancestry cases, 490 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094147 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Pasteurella) 124 Chinese ancestry cases, 494 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094148 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Mycoplasma) 120 Chinese ancestry cases, 498 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094149 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Candidatus_Phytoplasma) 117 Chinese ancestry cases, 501 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094150 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Candidatus_Arthromitus) 114 Chinese ancestry cases, 504 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094151 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Heliobacterium) 114 Chinese ancestry cases, 504 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094152 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Ureaplasma) 113 Chinese ancestry cases, 505 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094153 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Desulfotomaculum) 109 Chinese ancestry cases, 509 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094154 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Fluviicola) 108 Chinese ancestry cases, 510 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094155 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Desulfarculus) 104 Chinese ancestry cases, 514 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094156 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Brevibacillus) 104 Chinese ancestry cases, 514 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094157 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Cyanothece) 103 Chinese ancestry cases, 515 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094158 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Cupriavidus) 102 Chinese ancestry cases, 516 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094159 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thiomicrospira) 102 Chinese ancestry cases, 516 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094160 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Chlamydia) 100 Chinese ancestry cases, 518 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094161 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_multisaccharivorax) 427 Chinese ancestry cases, 191 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094246 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_mucosa) 423 Chinese ancestry cases, 195 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094247 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Serratia_odorifera) 419 Chinese ancestry cases, 199 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094248 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_subflava) 413 Chinese ancestry cases, 205 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094249 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Fusobacterium_nucleatum) 407 Chinese ancestry cases, 211 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094250 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Oribacterium_sp__oral_taxon_078) 405 Chinese ancestry cases, 213 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094251 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Filifactor_alocis) 404 Chinese ancestry cases, 214 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094252 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Escherichia_albertii) 404 Chinese ancestry cases, 214 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094253 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_cristatus) 400 Chinese ancestry cases, 218 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094254 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Edwardsiella_ictaluri/tarda) 400 Chinese ancestry cases, 218 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094255 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_gonorrhoeae) 395 Chinese ancestry cases, 223 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094256 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Enterobacter_asburiae) 394 Chinese ancestry cases, 224 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094257 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Gemella_haemolysans) 392 Chinese ancestry cases, 226 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094258 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_unclassified_Fusobacterium) 387 Chinese ancestry cases, 231 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094259 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Shewanella_putrefaciens) 383 Chinese ancestry cases, 235 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094260 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Streptococcus_sp__M334) 379 Chinese ancestry cases, 239 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094261 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Campylobacter_hominis) 455 Chinese ancestry cases, 163 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094237 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_nigrescens) 452 Chinese ancestry cases, 166 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094238 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_bryantii) 445 Chinese ancestry cases, 173 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094239 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Leuconostoc_mesenteroides) 444 Chinese ancestry cases, 174 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094240 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Vibrio_furnissii) 442 Chinese ancestry cases, 176 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094241 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Burkholderia_multivorans) 440 Chinese ancestry cases, 178 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094242 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Megasphaera_genomosp__type_1) 440 Chinese ancestry cases, 178 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094243 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_amnii) 432 Chinese ancestry cases, 186 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094244 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridium_hylemonae) 431 Chinese ancestry cases, 187 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094245 Genome-wide sequencing 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylleucine levels in elite athletes 490 individuals NA Illumina [275016] 4 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90133889 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylmethionine levels in elite athletes 490 individuals NA Illumina [275016] 4 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90133890 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylphenylalanine levels in elite athletes 490 individuals NA Illumina [275016] 8 gamma-glutamylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021142 GCST90133891 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylthreonine levels in elite athletes 490 individuals NA Illumina [275016] 5 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90133892 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ceramide (d16:1/24:1, d18:1/22:1) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133893 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamyltyrosine levels in elite athletes 490 individuals NA Illumina [275016] 15 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90133894 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylvaline levels in elite athletes 490 individuals NA Illumina [275016] 1 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90133895 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ceramide (d18:1/14:0, d16:1/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133896 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ceramide (d18:1/20:0, d16:1/22:0, d20:1/18:0) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133897 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glucose levels in elite athletes 490 individuals NA Illumina [275016] 3 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90133898 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glucuronate levels in elite athletes 490 individuals NA Illumina [275016] 6 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90133899 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glutamate levels in elite athletes 490 individuals NA Illumina [275016] 6 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90133900 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glutamine levels in elite athletes 490 individuals NA Illumina [275016] 6 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90133901 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ceramide (d18:2/24:1, d18:1/24:2) levels in elite athletes 490 individuals NA Illumina [275016] 9 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133902 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cerotoylcarnitine (C26) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133903 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycerate levels in elite athletes 490 individuals NA Illumina [275016] 7 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90133904 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Chiro-inositol levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133905 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycerol levels in elite athletes 490 individuals NA Illumina [275016] 1 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90133906 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cholesterol levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133907 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Choline phosphate levels in elite athletes 490 individuals NA Illumina [275016] 12 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133908 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycerophosphorylcholine (GPC) levels in elite athletes 490 individuals NA Illumina [275016] 7 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90133909 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycine levels in elite athletes 490 individuals NA Illumina [275016] 8 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90133910 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cis-4-decenoylcarnitine (C10:1) levels in elite athletes 490 individuals NA Illumina [275016] 12 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133911 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Decanoylcarnitine (C10) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133912 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycochenodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 8 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90133913 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoylcarnitine (C18:1) levels in elite athletes 490 individuals NA Illumina [275016] 8 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90134089 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134090 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ornithine levels in elite athletes 490 individuals NA Illumina [275016] 6 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90134091 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/23:1) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134092 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134093 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oxalate (ethanedioate) levels in elite athletes 490 individuals NA Illumina [275016] 6 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90134094 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. P-cresol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 11 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90134095 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/24:2) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134096 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoleate (16:1n7) levels in elite athletes 490 individuals NA Illumina [275016] 1 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90134097 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingosine 1-phosphate levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134098 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingosine levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134099 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stearate (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134100 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stearoyl sphingomyelin (d18:1/18:0) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134101 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stearoyl-arachidonoyl-glycerol (18:0/20:4) [1] levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134102 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stearoyl-arachidonoyl-glycerol (18:0/20:4) [2] levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134103 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stearoylcholine levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134104 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Suberate (octanedioate) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134105 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tauro-beta-muricholate levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134106 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Taurocholenate sulfate levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134107 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tauroursodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134108 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoylcarnitine (C16) levels in elite athletes 490 individuals NA Illumina [275016] 8 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90134109 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tricosanoyl sphingomyelin (d18:1/23:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134110 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pantothenate levels in elite athletes 490 individuals NA Illumina [275016] 3 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90134111 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Paraxanthine levels in elite athletes 490 individuals NA Illumina [275016] 7 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90134112 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Trimethylamine N-oxide levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134113 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d17:1/16:0, d18:1/15:0, d16:1/17:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134064 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N1-methyladenosine levels in elite athletes 490 individuals NA Illumina [275016] 3 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90134065 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d17:2/16:0, d18:2/15:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134066 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:0/18:0, d19:0/17:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134067 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N2,N2-dimethylguanosine levels in elite athletes 490 individuals NA Illumina [275016] 3 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90134068 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:0/20:0, d16:0/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134069 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134070 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134071 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134072 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/19:0, d19:1/18:0) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134073 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134074 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134075 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Nonadecanoate (19:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90134076 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/20:2, d18:2/20:1, d16:1/22:2) levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134077 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. O-sulfo-L-tyrosine levels in elite athletes 490 individuals NA Illumina [275016] 3 X-11423--O-sulfo-L-tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021231 GCST90134078 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Octadecanedioate levels in elite athletes 490 individuals NA Illumina [275016] 6 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90134079 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134080 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134081 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/22:2, d18:2/22:1, d16:1/24:2) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134082 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134083 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0) levels in elite athletes 490 individuals NA Illumina [275016] 13 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134084 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/14:0, d18:1/14:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134085 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134086 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134087 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphingomyelin (d18:2/21:0, d16:2/23:0) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134088 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Venous thromboembolism or factor VIII levels (pleiotropy) 32,610 European, African American, East Asian, South Asian or Hispanic individuals with measurements, 30,234 European or African American VTE cases, 172,122 European or African American VTE controls NA NR [NR] 28 factor VIII measurement, venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0004286 GCST90129536 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Venous thromboembolism or von Willebrand factor levels (pleiotropy) 30,234 European or African American VTE cases, 172,122 European or African American VTE controls, 46,354 European, African American or Hispanic individuals with measurements NA NR [NR] 32 venous thromboembolism, von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0004629 GCST90129537 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Venous thromboembolism or factor XI levels (pleiotropy) 16,169 European ancestry individuals with measurements, 30,234 European or African American VTE cases, 172,122 European or African American VTE controls NA NR [NR] 23 factor XI measurement, venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004694, http://www.ebi.ac.uk/efo/EFO_0004286 GCST90129538 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Venous thromboembolism or fibrinogen levels (pleiotropy) 120,246 European ancestry individuals with measurements, 30,234 European or African American VTE cases, 172,122 European or African American VTE controls NA NR [NR] 53 venous thromboembolism, fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0004623 GCST90129539 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Venous thromboembolism or tissue plasminogen activator levels (pleiotropy) 26,929 European ancestry individuals with measurements, 30,234 European or African American VTE cases, 172,122 European or African American VTE controls NA NR [NR] 18 venous thromboembolism, tissue plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0004791 GCST90129540 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Venous thromboembolism or plasminogen activator inhibitor 1 levels (pleiotropy) 19,599 European ancestry individuals with measurements, 30,234 European or African American VTE cases, 172,122 European or African American VTE controls NA NR [NR] 16 venous thromboembolism, plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0004792 GCST90129541 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Coronary artery disease or factor VII levels (pleiotropy) 172,122 European, South Asian or East Asian CAD cases, 566,864 European, South Asian or East Asian CAD controls, 27,495 European or African American individuals with measurements NA NR [NR] 80 coronary artery disease, factor VII measurement http://www.ebi.ac.uk/efo/EFO_0001645, http://www.ebi.ac.uk/efo/EFO_0004619 GCST90129542 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Coronary artery disease or factor VIII levels (pleiotropy) 172,122 European, South Asian or East Asian CAD cases, 566,864 European, South Asian or East Asian CAD controls, 32,610 European, African American, East Asian, South Asian or Hispanic individuals with measurements NA NR [NR] 82 factor VIII measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90129543 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Coronary artery disease or von Willebrand factor levels (pleiotropy) 172,122 European, South Asian or East Asian CAD cases, 566,864 European, South Asian or East Asian CAD controls, 46,354 European, African American or Hispanic individuals with measurements NA NR [NR] 88 von Willebrand factor measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004629, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90129544 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Coronary artery disease or factor XI levels (pleiotropy) 172,122 European, South Asian or East Asian CAD cases, 566,864 European, South Asian or East Asian CAD controls, 16,169 European ancestry individuals with measurements NA NR [NR] 81 factor XI measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004694, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90129545 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Coronary artery disease or fibrinogen levels (pleiotropy) 172,122 European, South Asian or East Asian CAD cases, 566,864 European, South Asian or East Asian CAD controls, 120,246 European ancestry individuals with measurements NA NR [NR] 107 fibrinogen measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90129546 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Coronary artery disease or tissue plasminogen activator levels (pleiotropy) 172,122 European, South Asian or East Asian CAD cases, 566,864 European, South Asian or East Asian CAD controls, 26,929 European ancestry individuals with measurements NA NR [NR] 52 tissue plasminogen activator measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004791, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90129547 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Coronary artery disease or plasminogen activator inhibitor 1 levels (pleiotropy) 172,122 European, South Asian or East Asian CAD cases, 566,864 European, South Asian or East Asian CAD controls, 19,599 European ancestry individuals with measurements NA NR [NR] 48 coronary artery disease, plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0001645, http://www.ebi.ac.uk/efo/EFO_0004792 GCST90129548 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Ischemic stroke or factor VII levels (pleiotropy) 27,495 European or African American individuals with measurements, 60,341 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke cases, 454,450 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke controls NA NR [NR] 17 Ischemic stroke, factor VII measurement http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0004619 GCST90129549 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Ischemic stroke or factor VIII levels (pleiotropy) 32,610 European, African American, East Asian, South Asian or Hispanic individuals with measurements, 60,341 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke cases, 454,450 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke controls NA NR [NR] 13 factor VIII measurement, Ischemic stroke http://www.ebi.ac.uk/efo/EFO_0004630, http://purl.obolibrary.org/obo/HP_0002140 GCST90129550 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Ischemic stroke or von Willebrand factor levels (pleiotropy) 60,341 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke cases, 454,450 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke controls, 46,354 European, African American or Hispanic individuals with measurements NA NR [NR] 20 Ischemic stroke, von Willebrand factor measurement http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0004629 GCST90129551 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Ischemic stroke or factor XI levels (pleiotropy) 16,169 European ancestry individuals with measurements, 60,341 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke cases, 454,450 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke controls NA NR [NR] 9 factor XI measurement, Ischemic stroke http://www.ebi.ac.uk/efo/EFO_0004694, http://purl.obolibrary.org/obo/HP_0002140 GCST90129552 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Ischemic stroke or fibrinogen levels (pleiotropy) 120,246 European ancestry individuals with measurements, 60,341 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke cases, 454,450 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke controls NA NR [NR] 38 Ischemic stroke, fibrinogen measurement http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0004623 GCST90129553 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Ischemic stroke or tissue plasminogen activator levels (pleiotropy) 60,341 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke cases, 454,450 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke controls, 26,929 European ancestry individuals with measurements NA NR [NR] 9 Ischemic stroke, tissue plasminogen activator measurement http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0004791 GCST90129554 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Ischemic stroke or plasminogen activator inhibitor 1 levels (pleiotropy) 60,341 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke cases, 454,450 European, African American, East Asian, South Asian, mixed Asian or Latin American ischemic stroke controls, 19,599 European ancestry individuals with measurements NA NR [NR] 9 Ischemic stroke, plasminogen activator inhibitor 1 measurement http://purl.obolibrary.org/obo/HP_0002140, http://www.ebi.ac.uk/efo/EFO_0004792 GCST90129555 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Factor VIII levels or von Willebrand factor levels (pleiotropy) 32,610 European, African American, East Asian, South Asian or Hispanic individuals with factor VIII measurements, 46,354 European, African American or Hispanic individuals with vWF measurements NA NR [NR] 19 factor VIII measurement, von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0004629 GCST90129556 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Fibrinogen levels or factor VII levels (pleiotropy) 120,246 European ancestry individuals with fibrinogen measurements, 27,495 European or African American individuals with factor VII measurements NA NR [NR] 39 fibrinogen measurement, factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0004619 GCST90129557 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Fibrinogen levels or tissue plasminogen activator levels (pleiotropy) 120,246 European ancestry individuals with fibrinogen measurements, 26,929 European ancestry individuals with tPA measurements NA NR [NR] 33 fibrinogen measurement, tissue plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0004791 GCST90129558 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Fibrinogen levels or plasminogen activator inhibitor 1 levels (pleiotropy) 120,246 European ancestry individuals with fibrinogen measurements, 19,599 European ancestry individuals with PAI1 measurements NA NR [NR] 33 fibrinogen measurement, plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0004792 GCST90129559 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Fibrinogen levels or factor VII levels or factor XI levels or tissue plasminogen activator levels (pleiotropy) 120,246 European ancestry individuals with fibrinogen measurements, 27,495 European or African American individuals with factor VII measurements, 16,169 European ancestry individuals with factor XI measurements, 26,929 European ancestry individuals with tPA measurements NA NR [NR] 40 factor XI measurement, fibrinogen measurement, tissue plasminogen activator measurement, factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004694, http://www.ebi.ac.uk/efo/EFO_0004623, http://www.ebi.ac.uk/efo/EFO_0004791, http://www.ebi.ac.uk/efo/EFO_0004619 GCST90129560 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Acisoga levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133538 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Alpha-hydroxyisocaproate levels in elite athletes 490 individuals NA Illumina [275016] 1 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133539 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Alpha-hydroxyisovalerate levels in elite athletes 490 individuals NA Illumina [275016] 11 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133540 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Argininate levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133541 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Beta-citrylglutamate levels in elite athletes 490 individuals NA Illumina [275016] 10 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133542 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Beta-hydroxyisovalerate levels in elite athletes 490 individuals NA Illumina [275016] 7 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133543 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Betaine levels in elite athletes 490 individuals NA Illumina [275016] 8 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133544 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Carboxyethyl-GABA levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133545 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cis-urocanate levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133546 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-methylhistidine levels in elite athletes 490 individuals NA Illumina [275016] 10 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90133547 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cysteine s-sulfate levels in elite athletes 490 individuals NA Illumina [275016] 7 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133548 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cysteine sulfinic acid levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133549 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-methylurate levels in elite athletes 490 individuals NA Illumina [275016] 8 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90133550 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-methylxanthine levels in elite athletes 490 individuals NA Illumina [275016] 4 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90133551 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cystine levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133552 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dimethylarginine (SDMA + ADMA) levels in elite athletes 490 individuals NA Illumina [275016] 8 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133553 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dopamine 3-O-sulfate levels in elite athletes 490 individuals NA Illumina [275016] 9 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133554 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glutarylcarnitine (C5-DC) levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133555 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Guanidinoacetate levels in elite athletes 490 individuals NA Illumina [275016] 10 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133556 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Guanidinosuccinate levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133557 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hydantoin-5-propionic acid levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133558 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hypotaurine levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133559 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Imidazole lactate levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133560 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Imidazole propionate levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133561 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Indole-3-carboxylic acid levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133562 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. (N(1) + N(8))-acetylspermidine levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133513 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-methylguanidine levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133514 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-methylimidazoleacetate levels in elite athletes 490 individuals NA Illumina [275016] 10 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133515 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-aminoadipate levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133516 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxy-3-methylvalerate levels in elite athletes 490 individuals NA Illumina [275016] 9 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133517 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxybutyrate/2-hydroxyisobutyrate levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133518 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxyphenylacetate levels in elite athletes 490 individuals NA Illumina [275016] 1 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133519 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-methylbutyrylcarnitine (C5) levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133520 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-methylbutyrylglycine levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133521 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-methylserine levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133522 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-oxoarginine levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133523 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-pyrrolidinone levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133524 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2,3-dihydroxy-2-methylbutyrate levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133525 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxy-2-ethylpropionate levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133526 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-indoxyl sulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133527 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methylglutaconate levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133528 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methylglutarylcarnitine (2) levels in elite athletes 490 individuals NA Illumina [275016] 3 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133529 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-guanidinobutanoate levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133530 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-hydroxyglutamate levels in elite athletes 490 individuals NA Illumina [275016] 8 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133531 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-hydroxyphenylpyruvate levels in elite athletes 490 individuals NA Illumina [275016] 9 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133532 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-imidazoleacetate levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133533 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-(galactosylhydroxy)-L-lysine levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133534 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-bromotryptophan levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133535 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-methylthioadenosine (MTA) levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133536 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 6-oxopiperidine-2-carboxylate levels in elite athletes 490 individuals NA Illumina [275016] 4 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133537 Genome-wide genotyping array 2021-12-06 30037793 Haapasalo K 2018-09-21 Infect Immun www.ncbi.nlm.nih.gov/pubmed/30037793 The Psoriasis Risk Allele HLA-C*06:02 Shows Evidence of Association with Chronic or Recurrent Streptococcal Tonsillitis. Tonsillitis 95 Finnish cases, 504 Finnish controls NA Illumina [100000] 2 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST012576 Targeted genotyping array [ImmunoChip] 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Ethanoligenens) 500 Chinese ancestry cases, 118 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094087 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Filifactor) 498 Chinese ancestry cases, 120 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094088 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Histophilus) 479 Chinese ancestry cases, 139 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094089 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Leuconostoc) 473 Chinese ancestry cases, 145 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094090 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Eremococcus) 468 Chinese ancestry cases, 150 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094091 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Actinobacillus) 465 Chinese ancestry cases, 153 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094092 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Cellulosilyticum) 458 Chinese ancestry cases, 160 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094093 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Pantoea) 456 Chinese ancestry cases, 162 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094094 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Pyramidobacter) 442 Chinese ancestry cases, 176 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094095 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Rahnella) 431 Chinese ancestry cases, 187 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094096 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Ornithinibacillus) 429 Chinese ancestry cases, 189 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094097 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Comamonas) 419 Chinese ancestry cases, 199 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094098 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thermosinus) 417 Chinese ancestry cases, 201 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094099 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Erwinia) 416 Chinese ancestry cases, 202 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094100 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Aeromonas) 411 Chinese ancestry cases, 207 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094101 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Shewanella) 409 Chinese ancestry cases, 209 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094102 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Alkaliphilus) 401 Chinese ancestry cases, 217 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094103 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Dickeya) 400 Chinese ancestry cases, 218 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094104 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Acetivibrio) 398 Chinese ancestry cases, 220 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094105 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Acidovorax) 391 Chinese ancestry cases, 227 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094106 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Dysgonomonas) 390 Chinese ancestry cases, 228 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094107 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thermoanaerobacter) 388 Chinese ancestry cases, 230 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094108 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thermoanaerobacterium) 384 Chinese ancestry cases, 234 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094109 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Thauera) 373 Chinese ancestry cases, 245 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094110 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Helicobacter) 369 Chinese ancestry cases, 249 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094111 Genome-wide sequencing 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Alpha-tocopherol levels in elite athletes 490 individuals NA Illumina [275016] 13 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90133764 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 10-undecenoate (11:1n1) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133765 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 12-HETE levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133766 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 12-HHTrE levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133767 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 12,13-DiHOME levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133768 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 13-HODE + 9-HODE levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133769 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 14-HDoHE/17-HDoHE levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133770 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 15-methylpalmitate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133771 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Androsterone sulfate levels in elite athletes 490 individuals NA Illumina [275016] 12 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90133772 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arabinose levels in elite athletes 490 individuals NA Illumina [275016] 5 arabinose measurement http://www.ebi.ac.uk/efo/EFO_0021030 GCST90133773 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 16-hydroxypalmitate levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133774 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 16a-hydroxy DHEA 3-sulfate levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133775 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 17-methylstearate levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133776 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 17alpha-hydroxypregnenolone 3-sulfate levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133777 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-aminoheptanoate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133778 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-aminooctanoate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133779 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-arachidonoylglycerol (20:4) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133780 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arginine levels in elite athletes 490 individuals NA Illumina [275016] 7 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90133781 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Asparagine levels in elite athletes 490 individuals NA Illumina [275016] 5 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90133782 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Aspartate levels in elite athletes 490 individuals NA Illumina [275016] 1 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90133783 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxyadipate levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133784 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxydecanoate levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133785 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxylaurate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133786 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxyoctanoate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133787 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Benzoate levels in elite athletes 490 individuals NA Illumina [275016] 2 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90133788 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Coprococcus_comes) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093937 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_uniformis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093938 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_dolichum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093939 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Granulicatella_adiacens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093940 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_coprophilus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093941 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Anaerostipes_caccae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093942 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_disiens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093943 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bifidobacterium_catenulatum-Bifidobacterium_pseudocatenulatum_complex) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093944 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Enterococcus_faecalis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093945 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Veillonella_atypica) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093946 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Streptococcus_sp__oral_taxon_071) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093947 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Parabacteroides_distasonis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093948 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_coprocola) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093949 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_sanguinis) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093950 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Citrobacter_sp__30_2) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093951 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Megasphaera_micronuciformis) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093952 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Gemella_sanguinis) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093953 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_australis) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093954 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_pneumoniae) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093955 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Peptostreptococcus_anaerobius) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093956 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Collinsella_aerofaciens) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093957 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_mitis) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093958 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Sutterella_wadsworthensis) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093959 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Porphyromonas_asaccharolytica) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093960 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Lachnospiraceae_oral_taxon_107) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093961 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_buccae) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093962 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Citrobacter_koseri) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093963 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_vestibularis) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093964 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Streptococcus_sp__C150) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093965 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Enterobacter_cloacae) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093966 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Enterobacter_hormaechei/cloacae) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093967 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Megasphaera_sp__UPII_135-E) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093968 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_gordonii) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093969 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Solobacterium_moorei) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093970 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Burkholderia_pseudomallei) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093971 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Klebsiella_oxytoca) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093972 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Salmonella_enterica) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093973 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Clostridium_sp__SY8519) 614 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093974 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Ruminococcus_champanellensis) 614 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093975 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Oxalobacter_formigenes) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093976 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Enterobacter_aerogenes) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093977 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Anaerofustis_stercorihominis) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093978 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Treponema_vincentii) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093979 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Mitsuokella_multacida) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093980 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Lactococcus_lactis) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093981 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Actinomyces_viscosus) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093982 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_spiroforme) 612 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093983 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Acidaminococcus_fermentans) 612 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093984 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bifidobacterium_adolescentis) 611 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093985 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bifidobacterium_breve) 611 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093986 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Fusobacterium) 610 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093987 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_tannerae) 610 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093988 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_suis) 610 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093989 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_oralis) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093990 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Ruminococcus_albus) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093991 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Tannerella_forsythia) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093992 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Megasphaera_elsdenii) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093993 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_mutans) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093994 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Desulfovibrio_piger) 605 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093995 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_saburreum) 603 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093996 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Klebsiella_pneumoniae) 601 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093997 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Akkermansia_muciniphila) 600 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093998 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Haemophilus_haemolyticus) 599 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093999 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Aggregatibacter_segnis) 596 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094000 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Haemophilus_influenzae) 596 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094001 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Klebsiella_pneumoniae/Klebsiella_variicola_group) 595 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094002 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Haemophilus_pittmaniae) 591 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094003 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bifidobacterium_bifidum) 591 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094004 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Enterobacteriaceae_bacterium_9_2_54FAA) 590 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094005 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_pyogenes) 589 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094006 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Mobiluncus_curtisii) 588 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094007 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bifidobacterium_animalis) 588 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094008 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Synergistetes) 579 Chinese ancestry cases, 39 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094009 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Fibrobacteres) 494 Chinese ancestry cases, 124 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094010 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Chloroflexi) 486 Chinese ancestry cases, 132 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094011 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Desulfobacterales) 88 Chinese ancestry cases, 530 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094037 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Sphingomonadales) 83 Chinese ancestry cases, 535 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094038 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Bacillaceae) 572 Chinese ancestry cases, 46 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094039 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Rhodobacteraceae) 571 Chinese ancestry cases, 47 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094040 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Vibrionaceae) 566 Chinese ancestry cases, 52 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094041 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Moraxellaceae) 539 Chinese ancestry cases, 79 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094042 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Corynebacteriaceae) 534 Chinese ancestry cases, 84 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094043 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Pseudomonadaceae) 505 Chinese ancestry cases, 113 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094044 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Comamonadaceae) 468 Chinese ancestry cases, 150 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094045 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Synergistaceae) 456 Chinese ancestry cases, 162 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094046 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Aeromonadaceae) 411 Chinese ancestry cases, 207 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094047 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Shewanellaceae) 409 Chinese ancestry cases, 209 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094048 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Helicobacteraceae) 369 Chinese ancestry cases, 249 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094049 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Alcaligenaceae) 360 Chinese ancestry cases, 258 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094050 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Succinivibrionaceae) 329 Chinese ancestry cases, 289 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094051 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Caulobacteraceae) 319 Chinese ancestry cases, 299 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094052 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Brachyspiraceae) 295 Chinese ancestry cases, 323 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094053 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Brucellaceae) 285 Chinese ancestry cases, 333 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094054 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Mycoplasmataceae) 214 Chinese ancestry cases, 404 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094055 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Methanobacteriaceae) 212 Chinese ancestry cases, 406 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094056 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Listeriaceae) 206 Chinese ancestry cases, 412 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094057 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Micrococcaceae) 167 Chinese ancestry cases, 451 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094058 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Burkholderiales_noname) 163 Chinese ancestry cases, 455 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094059 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Rhodocyclaceae) 141 Chinese ancestry cases, 477 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094060 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Chlamydiaceae) 100 Chinese ancestry cases, 518 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094061 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Cyanobacteria) 361 Chinese ancestry cases, 257 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094012 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Tenericutes) 347 Chinese ancestry cases, 271 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094013 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Euryarchaeota) 273 Chinese ancestry cases, 345 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094014 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Chlamydiae) 100 Chinese ancestry cases, 518 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094015 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Chlorobi) 96 Chinese ancestry cases, 522 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094016 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (phylum Deinococcus-Thermus) 77 Chinese ancestry cases, 541 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094017 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (class Synergistia) 456 Chinese ancestry cases, 162 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094018 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (class Mollicutes) 214 Chinese ancestry cases, 404 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094019 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (class Methanobacteria) 212 Chinese ancestry cases, 406 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094020 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (class Chlamydiia) 100 Chinese ancestry cases, 518 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094021 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Pseudomonadales) 576 Chinese ancestry cases, 42 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094022 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Rhodobacterales) 571 Chinese ancestry cases, 47 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094023 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Vibrionales) 566 Chinese ancestry cases, 52 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094024 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Aeromonadales) 506 Chinese ancestry cases, 112 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094025 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Synergistales) 456 Chinese ancestry cases, 162 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094026 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Alteromonadales) 411 Chinese ancestry cases, 207 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094027 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Caulobacterales) 319 Chinese ancestry cases, 299 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094028 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Rhizobiales) 315 Chinese ancestry cases, 303 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094029 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Mycoplasmatales) 214 Chinese ancestry cases, 404 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094030 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Methanobacteriales) 212 Chinese ancestry cases, 406 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094031 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Rhodocyclales) 141 Chinese ancestry cases, 477 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094032 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Chlamydiales) 100 Chinese ancestry cases, 518 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094033 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Rhodospirillales) 95 Chinese ancestry cases, 523 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094034 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Xanthomonadales) 94 Chinese ancestry cases, 524 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094035 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (order Cardiobacteriales) 92 Chinese ancestry cases, 526 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094036 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Cronobacter) 340 Chinese ancestry cases, 278 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094112 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Succinatimonas) 329 Chinese ancestry cases, 289 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094113 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Achromobacter) 328 Chinese ancestry cases, 290 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094114 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Caulobacter) 319 Chinese ancestry cases, 299 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094115 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Pectobacterium) 309 Chinese ancestry cases, 309 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094116 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Paenibacillus) 306 Chinese ancestry cases, 312 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094117 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Brachyspira) 295 Chinese ancestry cases, 323 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094118 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Kingella) 287 Chinese ancestry cases, 331 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094119 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Pseudoramibacter) 286 Chinese ancestry cases, 332 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094120 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Pelotomaculum) 282 Chinese ancestry cases, 336 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094121 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Brucella) 280 Chinese ancestry cases, 338 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094122 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Methylobacillus) 263 Chinese ancestry cases, 355 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094123 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Photorhabdus) 263 Chinese ancestry cases, 355 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094124 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Gardnerella) 255 Chinese ancestry cases, 363 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094125 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Sodalis) 251 Chinese ancestry cases, 367 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094126 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Candidatus_Hamiltonella) 235 Chinese ancestry cases, 383 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094127 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Riemerella) 232 Chinese ancestry cases, 386 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094128 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Bulleidia) 222 Chinese ancestry cases, 396 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094129 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Alicycliphilus) 218 Chinese ancestry cases, 400 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094130 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Listeria) 206 Chinese ancestry cases, 412 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094131 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Ralstonia) 196 Chinese ancestry cases, 422 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094132 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Dichelobacter) 195 Chinese ancestry cases, 423 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094133 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Methanobrevibacter) 194 Chinese ancestry cases, 424 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094134 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Desulfitobacterium) 192 Chinese ancestry cases, 426 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094135 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Streptobacillus) 190 Chinese ancestry cases, 428 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094136 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Xanthomonadaceae) 94 Chinese ancestry cases, 524 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094062 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Cardiobacteriaceae) 92 Chinese ancestry cases, 526 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094063 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Desulfobulbaceae) 88 Chinese ancestry cases, 530 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094064 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Sphingomonadaceae) 83 Chinese ancestry cases, 535 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094065 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (family Rhodospirillaceae) 78 Chinese ancestry cases, 540 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094066 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Turicibacter) 581 Chinese ancestry cases, 37 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094067 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Providencia) 579 Chinese ancestry cases, 39 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094068 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Victivallis) 576 Chinese ancestry cases, 42 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094069 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Shuttleworthia) 575 Chinese ancestry cases, 43 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094070 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Bacillus) 572 Chinese ancestry cases, 46 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094071 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Paracoccus) 571 Chinese ancestry cases, 47 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094072 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Vibrio) 566 Chinese ancestry cases, 52 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094073 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Proteus) 554 Chinese ancestry cases, 64 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094074 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Acinetobacter) 538 Chinese ancestry cases, 80 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094075 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Lawsonia) 537 Chinese ancestry cases, 81 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094076 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Corynebacterium) 534 Chinese ancestry cases, 84 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094077 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Finegoldia) 533 Chinese ancestry cases, 85 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094078 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Edwardsiella) 513 Chinese ancestry cases, 105 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094079 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Selenomonas) 511 Chinese ancestry cases, 107 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094080 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Yersinia) 511 Chinese ancestry cases, 107 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094081 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Slackia) 511 Chinese ancestry cases, 107 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094082 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Olsenella) 507 Chinese ancestry cases, 111 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094083 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Pseudomonas) 505 Chinese ancestry cases, 113 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094084 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Epulopiscium) 502 Chinese ancestry cases, 116 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094085 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (genus Serratia) 502 Chinese ancestry cases, 116 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094086 Genome-wide sequencing 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycocholate levels in elite athletes 490 individuals NA Illumina [275016] 6 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90133914 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Deoxycarnitine levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133915 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Diacylglycerol (16:1/18:2 [2], 16:0/18:3 [1]) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133916 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dihomo-linolenate (20:3n3 or n6) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133917 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dihomo-linolenoyl-choline levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133918 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dihomo-linolenoylcarnitine (20:3n3 or 6) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133919 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dihomo-linoleoylcarnitine (C20:2) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133920 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Docosadienoate (22:2n6) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133921 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Docosadioate levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133922 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Docosahexaenoylcarnitine (C22:6) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133923 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Docosahexaenoylcholine levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133924 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Docosapentaenoate (n3 DPA; 22:5n3) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133925 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Docosapentaenoate (n6 DPA; 22:5n6) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133926 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Eicosanodioate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133927 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycylvaline levels in elite athletes 490 individuals NA Illumina [275016] 6 glycylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021129 GCST90133928 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Eicosenoate (20:1) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133929 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Eicosenoylcarnitine (C20:1) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133930 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Guanosine levels in elite athletes 490 individuals NA Illumina [275016] 2 guanosine measurement http://www.ebi.ac.uk/efo/EFO_0021124 GCST90133931 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Erucate (22:1n9) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133932 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Etiocholanolone glucuronide levels in elite athletes 490 individuals NA Illumina [275016] 9 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133933 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Heptanoate (7:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 heptanoate 7:0 measurement http://www.ebi.ac.uk/efo/EFO_0021104 GCST90133934 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glutarate (pentanedioate) levels in elite athletes 490 individuals NA Illumina [275016] 10 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133935 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hexadecanedioate levels in elite athletes 490 individuals NA Illumina [275016] 1 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90133936 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycerol 3-phosphate levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133937 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycerophosphoethanolamine levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133938 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hippurate levels in elite athletes 490 individuals NA Illumina [275016] 4 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90133940 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Histidine levels in elite athletes 490 individuals NA Illumina [275016] 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90133941 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycochenodeoxycholate glucuronide (1) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133942 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Homoarginine levels in elite athletes 490 individuals NA Illumina [275016] 10 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST90133943 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Homocitrulline levels in elite athletes 490 individuals NA Illumina [275016] 2 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90133944 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Homostachydrine levels in elite athletes 490 individuals NA Illumina [275016] 5 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90133945 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. HWESASXX levels in elite athletes 490 individuals NA Illumina [275016] 5 HWESASXX measurement http://www.ebi.ac.uk/efo/EFO_0021147 GCST90133946 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycochenodeoxycholate sulfate levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133947 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hydroquinone sulfate levels in elite athletes 490 individuals NA Illumina [275016] 2 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90133948 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycocholenate sulfate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133949 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycodeoxycholate sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133950 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hypoxanthine levels in elite athletes 490 individuals NA Illumina [275016] 2 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90133951 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycohyocholate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133952 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycolithocholate sulfate levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133953 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycolithocholate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133954 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Indoleacetate levels in elite athletes 490 individuals NA Illumina [275016] 5 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90133955 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycosyl ceramide (d18:1/20:0, d16:1/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133956 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Indolelactate levels in elite athletes 490 individuals NA Illumina [275016] 2 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90133957 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Indolepropionate levels in elite athletes 490 individuals NA Illumina [275016] 4 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90133958 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycosyl ceramide (d18:1/23:1, d17:1/24:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133959 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Inosine levels in elite athletes 490 individuals NA Illumina [275016] 1 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90133960 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycosyl ceramide (d18:2/24:1, d18:1/24:2) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133961 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133962 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycosyl-N-behenoyl-sphingosine (d18:1/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133963 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycerophosphoinositol levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133939 Genome-wide genotyping array 2022-02-16 34706928 Scannell Bryan M 2021-10-27 J Epidemiol Community Health www.ncbi.nlm.nih.gov/pubmed/34706928 Associations between age of menarche and genetic variation in women of African descent: genome-wide association study and polygenic score analysis. Age at menarche 3,145 African American, African Barbadian or Nigerian ancestry individuals NA Illumina [16413036] (imputed) 1 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90094651 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Veillonella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032643 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Victivallis sp002998355 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032644 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Absiella dolichum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032172 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Acetobacteraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032173 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Acetobacterales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032174 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Achromobacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032175 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Acidaminococcus fermentans abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032176 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Acidaminococcus sp900315205 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032177 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Acidobacteriales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032178 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Actinobacteria abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032179 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Actinobacteriota abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032180 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Actinomycetales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032181 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Agathobacter sp000434275 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032182 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Akkermansia muciniphila B abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032183 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Aliivibrio abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032184 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Alistipes shahii abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032185 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Alistipes abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032186 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Alloprevotella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032187 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Alteromonadaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032188 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. An181 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032189 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. An7 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032190 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Anaeromassilibacillus sp001305115 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032191 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Aneurinibacillaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032192 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Aneurinibacillales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032193 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. AR31 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032194 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Atopobiaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032195 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Aureimonas abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032196 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Azorhizobium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032197 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacillaceae A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032198 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacillales A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032199 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacilli A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032200 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacillus AY abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032201 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacillus C abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032202 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacillus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032203 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacillus U abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032204 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacillus velezensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032205 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides A plebeius A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032206 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides A plebeius abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032207 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032208 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides clarus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032209 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides eggerthii abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032210 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides faecis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032211 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides intestinalis A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032212 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides sp002160055 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032213 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides sp003545565 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032214 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides stercoris abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032215 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bacteroides thetaiotaomicron abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032216 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Barnesiellaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032217 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Barnesiella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032218 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacteriaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032219 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA6382 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032618 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA6398 sp002451695 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032619 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA6398 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032620 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA644 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032621 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA6960 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032622 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA7102 sp002315655 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032623 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA7177 sp002491225 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032624 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA7177 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032625 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA7182 sp002491115 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032626 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA7182 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032627 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA737 sp002451855 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032628 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA737 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032629 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA7703 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032630 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA7748 sp900314535 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032631 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA8517 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032632 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA8621 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032633 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA8904 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032634 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA9475 sp002161235 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032635 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA9475 sp002161675 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032636 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBP9 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032637 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UCG-010 sp003150215 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032638 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UNC496MF abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032639 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. V9D3004 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032640 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Veillonellaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032641 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Veillonella rogosae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032642 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium adolescentis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032220 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium angulatum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032221 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium bifidum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032222 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium breve abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032223 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium catenulatum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032224 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium infantis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032225 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium kashiwanohense abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032226 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium longum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032227 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium pseudocatenulatum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032228 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium ruminantium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032229 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bifidobacterium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032230 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Bin127 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032231 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Blautia A sp000285855 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032232 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Blautia A sp002159835 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032233 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Blautia A sp900066145 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032234 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Blautia A sp900066355 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032235 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Blautia hansenii abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032236 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Blautia sp000436935 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032237 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Blautia sp001304935 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032238 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Borreliaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032239 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Borreliales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032240 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Brachyspiraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032241 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Brachyspirae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032242 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Brachyspirales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032243 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Brachyspira abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032244 Genome-wide genotyping array 2022-02-18 34719683 Park JS 2021-11-01 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34719683 Genome-wide meta-analysis revealed several genetic loci associated with serum uric acid levels in Korean population: an analysis of Korea Biobank data. Serum uric acid levels 60,585 Korean ancestry individuals NA NR [7104359] (imputed) 13 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90094591 Genome-wide genotyping array 2022-05-13 35099328 Lee ML 2022-01-31 Phlebology www.ncbi.nlm.nih.gov/pubmed/35099328 A genome-wide association study for varicose veins. Varicose veins 96 Taiwanese ancestry cases, 1,000 Taiwanese ancestry controls NA Illumina [246512] 10 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90102601 Genome-wide genotyping array 2022-05-13 35099328 Lee ML 2022-01-31 Phlebology www.ncbi.nlm.nih.gov/pubmed/35099328 A genome-wide association study for varicose veins. Varicose veins (mild vs severe) 39 Taiwanese ancestry mild cases, 57 Taiwanese ancestry severe cases NA Illumina [246512] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90102602 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-(4-hydroxyphenyl)lactate levels in elite athletes 490 individuals NA Illumina [275016] 4 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90133664 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133665 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-aminoisobutyrate levels in elite athletes 490 individuals NA Illumina [275016] 6 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90133666 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (CMPF) levels in elite athletes 490 individuals NA Illumina [275016] 7 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90133667 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133668 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-stearoyl)-GPE (P-18:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133669 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-arachidonoyl-GPA (20:4) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133670 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-arachidonoyl-GPC (20:4n6) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133671 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-arachidonoyl-GPE (20:4n6) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133672 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-arachidonoyl-GPI (20:4) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133673 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-arachidonylglycerol (20:4) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133674 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-dihomo-linolenylglycerol (20:3) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133675 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxyisobutyrate levels in elite athletes 490 individuals NA Illumina [275016] 6 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90133676 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-dihomo-linoleoylglycerol (20:2) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133677 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-lignoceroyl-GPC (24:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133678 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linolenoyl-GPC (18:3) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133679 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linolenoylglycerol (18:3) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133680 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133681 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133682 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linoleoyl-GPC (18:2) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133683 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methoxytyrosine levels in elite athletes 490 individuals NA Illumina [275016] 10 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90133684 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linoleoyl-GPE (18:2) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133685 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linoleoyl-GPG (18:2) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133686 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methyl-2-oxobutyrate levels in elite athletes 490 individuals NA Illumina [275016] 5 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90133687 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methyl-2-oxovalerate levels in elite athletes 490 individuals NA Illumina [275016] 4 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90133688 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133714 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-methyl-2-oxopentanoate levels in elite athletes 490 individuals NA Illumina [275016] 3 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90133715 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133716 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133717 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-vinylphenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90133718 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133719 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133720 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133721 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133722 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133723 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 14 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133724 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133725 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133726 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-palmitoleoyl-GPC (16:0/16:1) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133727 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-methyluridine (ribothymidine) levels in elite athletes 490 individuals NA Illumina [275016] 3 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90133728 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-oxoproline levels in elite athletes 490 individuals NA Illumina [275016] 5 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90133729 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133730 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-GPA (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133731 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-GPC (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133732 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-GPE (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133733 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-GPG (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133734 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoyl-GPI (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133735 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoylglycerol (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133736 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3beta,17beta-diol disulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90133737 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-pentadecanoylglycerol (15:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133738 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linoleoyl-GPI (18:2) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133689 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-linoleoylglycerol (18:2) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133690 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133691 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133692 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methylhistidine levels in elite athletes 490 individuals NA Illumina [275016] 2 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90133693 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methylxanthine levels in elite athletes 490 individuals NA Illumina [275016] 3 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90133694 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-phenylpropionate (hydrocinnamate) levels in elite athletes 490 individuals NA Illumina [275016] 6 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90133695 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-ureidopropionate levels in elite athletes 490 individuals NA Illumina [275016] 3 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90133696 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-myristoylglycerol (14:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133697 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133698 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133699 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoyl-GPA (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133700 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-acetamidobutanoate levels in elite athletes 490 individuals NA Illumina [275016] 4 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90133701 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoyl-GPC (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133702 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoyl-GPE (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133703 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoyl-GPG (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133704 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-ethylphenylsulfate levels in elite athletes 490 individuals NA Illumina [275016] 9 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90133705 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoyl-GPI (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133706 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-oleoylglycerol (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133707 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133708 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoleoyl-2-linoleoyl-GPC (16:1/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133709 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoleoyl-GPA (16:1) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133710 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-hydroxyhippurate levels in elite athletes 490 individuals NA Illumina [275016] 3 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90133711 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoleoyl-GPC (16:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133712 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-palmitoleoylglycerol (16:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133713 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Chenodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 11 chenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010471 GCST90133815 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methyladipate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133816 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cholate levels in elite athletes 490 individuals NA Illumina [275016] 8 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90133817 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3beta-hydroxy-5-cholestenoate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133821 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3beta,7alpha-dihydroxy-5-cholestenoate levels in elite athletes 490 individuals NA Illumina [275016] 10 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133822 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-cholesten-3-one levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133823 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-HDoHE levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133824 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Citrate levels in elite athletes 490 individuals NA Illumina [275016] 3 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90133825 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cortisol levels in elite athletes 490 individuals NA Illumina [275016] 2 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90133826 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cortisone levels in elite athletes 490 individuals NA Illumina [275016] 4 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90133827 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Creatine levels in elite athletes 490 individuals NA Illumina [275016] 10 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90133828 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Creatinine levels in elite athletes 490 individuals NA Illumina [275016] 3 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90133829 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cystathionine levels in elite athletes 490 individuals NA Illumina [275016] 6 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90133830 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-dodecenoate (12:1n7) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133831 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-HEPE levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133832 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cysteine-glutathione disulfide levels in elite athletes 490 individuals NA Illumina [275016] 6 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90133833 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cysteine levels in elite athletes 490 individuals NA Illumina [275016] 6 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90133834 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-HETE levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133835 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-HETrE levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133836 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3alpha,17alpha-diol disulfate levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133837 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dehydroisoandrosterone sulfate (DHEA-S) levels in elite athletes 490 individuals NA Illumina [275016] 1 dehydroisoandrosterone sulfate DHEA-S measurement http://www.ebi.ac.uk/efo/EFO_0021119 GCST90133838 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Spirochaetales) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093717 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Verrucomicrobiales) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093718 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Neisseriales) 596 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093719 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Flavobacteriaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093720 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Peptostreptococcaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093721 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Lachnospiraceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093722 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Coriobacteriaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093723 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Enterococcaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093724 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Pasteurellaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093725 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Prevotellaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093726 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Carnobacteriaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093727 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Veillonellaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093728 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Clostridiales_noname) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093729 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Clostridiaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093730 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Actinomycetaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093731 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Porphyromonadaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093732 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Burkholderiaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093733 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Acidaminococcaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093734 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Rikenellaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093735 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Desulfovibrionaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093736 Genome-wide sequencing 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxysebacate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133814 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Yersinia_enterocolitica) 173 Chinese ancestry cases, 445 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094337 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Prevotella_sp__oral_taxon_299) 171 Chinese ancestry cases, 447 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094338 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Erwinia_pyrifoliae) 169 Chinese ancestry cases, 449 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094339 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_johnsonii) 168 Chinese ancestry cases, 450 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094340 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Thioalkalivibrio_sulfidophilus) 168 Chinese ancestry cases, 450 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094341 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Vibrio_alginolyticus) 166 Chinese ancestry cases, 452 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094342 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Parvimonas_sp__oral_taxon_393) 164 Chinese ancestry cases, 454 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094343 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Actinobacillus_minor) 164 Chinese ancestry cases, 454 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094344 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_iners) 156 Chinese ancestry cases, 462 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094345 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Anaerococcus_lactolyticus) 153 Chinese ancestry cases, 465 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094346 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_equinus) 153 Chinese ancestry cases, 465 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094347 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Serratia_plymuthica/odorifera) 149 Chinese ancestry cases, 469 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094348 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Dickeya_dadantii) 149 Chinese ancestry cases, 469 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094349 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Aeromonas_caviae) 149 Chinese ancestry cases, 469 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094350 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Parvimonas_sp__oral_taxon_110) 138 Chinese ancestry cases, 480 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094351 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Dialister_micraerophilus) 134 Chinese ancestry cases, 484 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094352 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Pseudomonas_aeruginosa) 130 Chinese ancestry cases, 488 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094353 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_equi) 124 Chinese ancestry cases, 494 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094354 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_pseudoporcinus) 121 Chinese ancestry cases, 497 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094355 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Gardnerella_vaginalis) 120 Chinese ancestry cases, 498 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094356 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Leuconostoc_lactis) 119 Chinese ancestry cases, 499 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094357 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_plantarum) 119 Chinese ancestry cases, 499 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094358 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence ([Eubacterium]_yurii) 114 Chinese ancestry cases, 504 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094359 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_lactamica) 113 Chinese ancestry cases, 505 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094360 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Syntrophobacter_fumaroxidans) 113 Chinese ancestry cases, 505 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094361 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Ureaplasma_urealyticum) 111 Chinese ancestry cases, 507 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094362 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Providencia_stuartii) 111 Chinese ancestry cases, 507 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094363 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Proteus_penneri) 107 Chinese ancestry cases, 511 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094364 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Serratia_proteamaculans) 106 Chinese ancestry cases, 512 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094365 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Desulfarculus_baarsii) 105 Chinese ancestry cases, 513 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094366 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Anaerococcus_hydrogenalis) 105 Chinese ancestry cases, 513 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094367 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Enterococcus_casseliflavus) 102 Chinese ancestry cases, 516 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094368 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Simonsiella_muelleri) 95 Chinese ancestry cases, 523 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094369 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Pasteurella_multocida) 94 Chinese ancestry cases, 524 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094370 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Chlamydia_trachomatis) 94 Chinese ancestry cases, 524 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094371 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridium_botulinum) 92 Chinese ancestry cases, 526 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094372 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Acinetobacter_radioresistens) 92 Chinese ancestry cases, 526 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094373 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactobacillus_helveticus) 89 Chinese ancestry cases, 529 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094374 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_downei) 89 Chinese ancestry cases, 529 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094375 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Anaerococcus_prevotii) 84 Chinese ancestry cases, 534 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094376 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Streptococcus_sp__oral_taxon_056) 83 Chinese ancestry cases, 535 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094377 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Dichelobacter_nodosus) 79 Chinese ancestry cases, 539 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094378 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridium_sporogenes/botulinum) 79 Chinese ancestry cases, 539 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094379 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Clostridium_proteoclasticum) 76 Chinese ancestry cases, 542 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094380 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Peptoniphilus_sp__oral_taxon_375) 76 Chinese ancestry cases, 542 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094381 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_parauberis) 75 Chinese ancestry cases, 543 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094382 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Prevotella_oralis) 74 Chinese ancestry cases, 544 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094383 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Streptococcus_urinalis) 72 Chinese ancestry cases, 546 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094384 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Acinetobacter_lwoffii) 71 Chinese ancestry cases, 547 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094385 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Lactococcus_garvieae) 70 Chinese ancestry cases, 548 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094386 Genome-wide sequencing 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methylglutarate/2-methylglutarate levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133818 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3b-hydroxy-5-cholenoic acid levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133819 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Choline levels in elite athletes 490 individuals NA Illumina [275016] 3 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90133820 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Negativicutes) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093692 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Actinobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093693 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Clostridia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093694 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Bacilli) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093695 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Gammaproteobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093696 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Flavobacteriia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093697 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Desulfuromonas_acetoxidans) 68 Chinese ancestry cases, 550 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094388 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Verrucomicrobiae) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093699 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Alphaproteobacteria) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093700 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Burkholderiales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093701 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Erwinia_tasmaniensis) 66 Chinese ancestry cases, 552 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094391 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Clostridiales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093703 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Neisseria_elongata) 62 Chinese ancestry cases, 556 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094393 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Desulfovibrionales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093705 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Dehalogenimonas_lykanthroporepellens) 62 Chinese ancestry cases, 556 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094395 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Fusobacteriales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093707 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota enterotype (Prevotella vs Bacteroides) 178 Chinese ancestry cases, 440 Chinese ancestry controls 190 Chinese ancestry cases, 473 Chinese ancestry controls NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094397 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Selenomonadales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093709 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Lactobacillales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093710 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Enterobacteriales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093711 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Bifidobacteriales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093712 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Verrucomicrobia) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093683 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Lentisphaerae) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093684 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Spirochaetes) 606 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093685 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Deltaproteobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093686 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Rhodospirillum_rubrum) 68 Chinese ancestry cases, 550 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094387 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Spirochaetia) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093698 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_gamma_proteobacterium_HdN1) 67 Chinese ancestry cases, 551 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094389 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Prevotella_sp__oral_taxon_317) 67 Chinese ancestry cases, 551 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094390 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Erysipelotrichales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093702 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (Anaerococcus_tetradius) 65 Chinese ancestry cases, 553 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094392 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Campylobacterales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093704 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota presence (unclassified_Geobacter_sp__M18) 62 Chinese ancestry cases, 556 Chinese ancestry controls 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094394 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Flavobacteriales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093706 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota (beta diversity) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90094396 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Pasteurellales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093708 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Bacteroidetes) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093678 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Fusobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093679 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Actinobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093680 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Proteobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093681 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (phylum Firmicutes) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093682 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Coriobacteriales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093713 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Actinomycetales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093714 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Bacteroidales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093715 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (order Bacillales) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093716 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Fusobacteriia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093687 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Erysipelotrichia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093688 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Epsilonproteobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093689 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Bacteroidia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093690 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (class Betaproteobacteria) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093691 Genome-wide sequencing 2022-02-18 34975738 Winsvold BS 2021-12-17 Front Neurol www.ncbi.nlm.nih.gov/pubmed/34975738 Genome-Wide Association Study of 2,093 Cases With Idiopathic Polyneuropathy and 445,256 Controls Identifies First Susceptibility Loci. Idiopathic polyneuropathy 1,147 European ancestry cases, 62,204 European ancestry controls 946 European ancestry cases, 383,052 European ancestry controls Illumina [13629169] (imputed) 2 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90094686 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. RUG147 sp900315495 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032543 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. RUG147 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032544 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. RUG420 sp900317985 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032545 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. RUG472 sp900319345 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032546 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. RUG472 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032547 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus A sp000432335 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032548 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus C sp000437255 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032549 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus D bicirculans abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032550 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus D abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032551 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus E sp003521625 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032552 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus E sp900100595 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032553 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus E sp900314705 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032554 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ruminococcus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032555 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Saccharofermentanaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032556 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Saccharomonospora abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032557 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. SAR324 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032558 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. SM23-33 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032559 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Sorangium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032560 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Spirillospora abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032561 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Spirochaetia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032562 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Sporomusales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032563 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Staphylococcus A fleurettii abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032564 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Staphylococcus aureus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032565 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Stappia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032566 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Streptacidiphilus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032567 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA11471 sp000434215 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032593 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA11471 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032594 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1191 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032595 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA11963 sp002362595 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032596 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA11963 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032597 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1206 sp000433115 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032598 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1375 sp002305795 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032599 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1407 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032600 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1409 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032601 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1417 sp003531055 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032602 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1446 sp002329245 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032603 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1448 sp002329405 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032604 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1448 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032605 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1611 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032606 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1777 sp002320035 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032607 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1777 sp900316255 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032608 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1777 sp900319275 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032609 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1777 sp900319835 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032610 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA2658 sp002841545 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032611 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA2821 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032612 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA2922 sp900313925 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032613 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA3282 sp002493835 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032614 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA3792 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032615 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA3855 sp900316885 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032616 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA5394 sp002409725 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032617 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Streptococcus sanguinis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032568 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Succiniclasticum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032569 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Succinivibrionaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032570 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Succinivibrio abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032571 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Syntrophomonadia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032572 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Syntrophorhabdaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032573 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Syntrophorhabdia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032574 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Tannerellaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032575 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Tepidanaerobacteraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032576 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Terrisporobacter othiniensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032577 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Terrisporobacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032578 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Thermococcaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032579 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Thermococci abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032580 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Thermoplasmatota abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032581 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Thermoprotei abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032582 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Thioalkalivibrionaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032583 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. TMED109 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032584 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Treponema D abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 20 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032585 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Treponemataceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032586 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Turicibacteraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032587 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Turicibacter sp001543345 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032588 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Turicibacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032589 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1033 sp001695555 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032590 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1066 sp900317515 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032591 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. UBA1066 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032592 Genome-wide genotyping array 2021-12-23 33693626 Jamieson SE 2021-03-09 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/33693626 Common and rare genetic variants that could contribute to severe otitis media in an Australian Aboriginal population. Otitis media 21 Martu ancestry cases, 370 Martu ancestry controls NA Illumina [6724284] (imputed) 21 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST90090962 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxyhippurate levels in elite athletes 490 individuals NA Illumina [275016] 12 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134174 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxypyridine sulfate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134175 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methoxycatechol sulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134176 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methyl catechol sulfate (1) levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134177 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-methyl catechol sulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134178 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3,7-dimethylurate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134179 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-acetylphenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134180 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-allylphenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134181 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-hydroxychlorothalonil levels in elite athletes 490 individuals NA Illumina [275016] 8 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134182 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-hydroxycoumarin levels in elite athletes 490 individuals NA Illumina [275016] 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134183 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-methylcatechol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134184 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-vinylguaiacol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134185 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stachydrine levels in elite athletes 490 individuals NA Illumina [275016] 5 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90134186 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-acetylamino-6-amino-3-methyluracil levels in elite athletes 490 individuals NA Illumina [275016] 9 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134187 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stearidonate (18:4n3) levels in elite athletes 490 individuals NA Illumina [275016] 1 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90134188 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Indoleacetylglutamine levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133563 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isobutyrylcarnitine (C4) levels in elite athletes 490 individuals NA Illumina [275016] 8 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133564 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isobutyrylglycine levels in elite athletes 490 individuals NA Illumina [275016] 1 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133565 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isovalerylcarnitine (C5) levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133566 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isovalerylglycine levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133567 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Kynurenate levels in elite athletes 490 individuals NA Illumina [275016] 2 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133568 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-acetylphenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134173 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5-acetylamino-6-formylamino-3-methyluracil levels in elite athletes 490 individuals NA Illumina [275016] 7 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134189 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 6-hydroxyindole sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134190 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Acesulfame levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134191 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Stearoylcarnitine (C18) levels in elite athletes 490 individuals NA Illumina [275016] 11 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90134192 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Beta-guanidinopropanoate levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134193 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Betonicine levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134194 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Succinate levels in elite athletes 490 individuals NA Illumina [275016] 5 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90134195 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Carotene diol (1) levels in elite athletes 490 individuals NA Illumina [275016] 3 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134196 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Succinylcarnitine (C4-DC) levels in elite athletes 490 individuals NA Illumina [275016] 5 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90134197 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sucrose levels in elite athletes 490 individuals NA Illumina [275016] 5 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90134198 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Carotene diol (2) levels in elite athletes 490 individuals NA Illumina [275016] 3 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134199 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cinnamoylglycine levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134200 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Diglycerol levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134201 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Taurine levels in elite athletes 490 individuals NA Illumina [275016] 1 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90134202 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dihydroferulic acid levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134203 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Taurochenodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 14 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90134204 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Taurocholate levels in elite athletes 490 individuals NA Illumina [275016] 3 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90134205 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dimethyl sulfone levels in elite athletes 490 individuals NA Illumina [275016] 9 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134206 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Taurodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 6 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90134207 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Taurolithocholate 3-sulfate levels in elite athletes 490 individuals NA Illumina [275016] 8 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90134208 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ectoine levels in elite athletes 490 individuals NA Illumina [275016] 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134209 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tetradecanedioate levels in elite athletes 490 individuals NA Illumina [275016] 3 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90134210 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Theobromine levels in elite athletes 490 individuals NA Illumina [275016] 6 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90134211 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Theophylline levels in elite athletes 490 individuals NA Illumina [275016] 6 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90134212 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Eugenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134213 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Threonate levels in elite athletes 490 individuals NA Illumina [275016] 3 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90134214 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Threonine levels in elite athletes 490 individuals NA Illumina [275016] 3 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90134215 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ferulic acid 4-sulfate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134216 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Thymol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90134217 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Thyroxine levels in elite athletes 490 individuals NA Illumina [275016] 4 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90134218 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gluconate levels in elite athletes 490 individuals NA Illumina [275016] 8 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134219 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Indolin-2-one levels in elite athletes 490 individuals NA Illumina [275016] 3 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134220 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isoeugenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134221 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Lanthionine levels in elite athletes 490 individuals NA Illumina [275016] 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134222 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Methyl glucopyranoside (alpha + beta) levels in elite athletes 490 individuals NA Illumina [275016] 7 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134223 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Methyl-4-hydroxybenzoate sulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134224 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tryptophan betaine levels in elite athletes 490 individuals NA Illumina [275016] 4 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90134225 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tryptophan levels in elite athletes 490 individuals NA Illumina [275016] 10 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90134226 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-(2-furoyl)glycine levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134227 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tyrosine levels in elite athletes 490 individuals NA Illumina [275016] 5 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90134228 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-methylpipecolate levels in elite athletes 490 individuals NA Illumina [275016] 9 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134229 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. O-cresol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134230 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Urate levels in elite athletes 490 individuals NA Illumina [275016] 7 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90134231 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Perfluorooctanesulfonic acid (PFOS) levels in elite athletes 490 individuals NA Illumina [275016] 9 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134232 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Uridine levels in elite athletes 490 individuals NA Illumina [275016] 5 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90134233 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ursodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 5 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90134234 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Valerate levels in elite athletes 490 individuals NA Illumina [275016] 4 valerate measurement http://www.ebi.ac.uk/efo/EFO_0021112 GCST90134235 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Valine levels in elite athletes 490 individuals NA Illumina [275016] 2 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90134236 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pyrraline levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134237 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Retinal levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134238 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Succinimide levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134239 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134240 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tartarate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134241 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-palmitoyl-sphingadienine (d18:2/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134014 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-palmitoyl-sphinganine (d18:0/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134015 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-palmitoyl-sphingosine (d18:1/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134016 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-palmitoylglycine levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134017 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetyl-beta-alanine levels in elite athletes 490 individuals NA Illumina [275016] 8 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90134018 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-palmitoylserine levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134019 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-palmitoyltaurine levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134020 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylarginine levels in elite athletes 490 individuals NA Illumina [275016] 7 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90134021 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-stearoyl-sphingosine (d18:1/18:0) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134022 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-stearoyltaurine levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134023 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Nervonoylcarnitine (C24:1) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134024 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Octanoylcarnitine (C8) levels in elite athletes 490 individuals NA Illumina [275016] 13 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134025 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleate/vaccenate (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134026 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoyl ethanolamide levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134027 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoyl-arachidonoyl-glycerol (18:1/20:4) [1] levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134028 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoyl-linoleoyl-glycerol (18:1/18:2) [1] levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134031 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoyl-linoleoyl-glycerol (18:1/18:2) [2] levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134032 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoyl-oleoyl-glycerol (18:1/18:1) [1] levels in elite athletes 490 individuals NA Illumina [275016] 12 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134033 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylmethionine levels in elite athletes 490 individuals NA Illumina [275016] 7 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90134034 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylneuraminate levels in elite athletes 490 individuals NA Illumina [275016] 3 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90134035 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoleoyl-arachidonoyl-glycerol (16:1/20:4) [2] levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134039 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetyltaurine levels in elite athletes 490 individuals NA Illumina [275016] 2 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90134040 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoleoyl-linoleoyl-glycerol (16:1/18:2) [1] levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134041 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoleoylcarnitine (C16:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134042 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoloelycholine levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134043 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134044 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoyl ethanolamide levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134045 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoyl-arachidonoyl-glycerol (16:0/20:4) [1] levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134046 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoyl-linoleoyl-glycerol (16:0/18:2) [1] levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134047 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoyl-linoleoyl-glycerol (16:0/18:2) [2] levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134048 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoyl-oleoyl-glycerol (16:0/18:1) [1] levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134049 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoyl-oleoyl-glycerol (16:0/18:1) [2] levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134050 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitoylcholine levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134051 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pentadecanoate (15:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134052 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pimelate (heptanedioate) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134053 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pregn steroid monosulfate C21H34O5S levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134054 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pregnanediol-3-glucuronide levels in elite athletes 490 individuals NA Illumina [275016] 9 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134055 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pregnanolone/allopregnanolone sulfate levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134056 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pregnen-diol disulfate C21H34O8S2 levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134057 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pregnenolone sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134058 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Propionylcarnitine (C3) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134059 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Propionylglycine levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134060 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sebacate (decanedioate) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134061 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphinganine-1-phosphate levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134062 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sphinganine levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134063 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylglycine levels in elite athletes 490 individuals NA Illumina [275016] 3 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90134029 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoyl-arachidonoyl-glycerol (18:1/20:4) [2] levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134030 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoyl-oleoyl-glycerol (18:1/18:1) [2] levels in elite athletes 490 individuals NA Illumina [275016] 13 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134036 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Oleoylcholine levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134037 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Palmitate (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134038 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella sp000434975 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032518 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella sp000436915 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032519 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella sp002437285 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032520 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella sp002437565 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032521 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella sp002933775 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032522 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella sp900317685 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032523 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella sp900318625 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032524 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Propionibacterium freudenreichii abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032525 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Proteus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032526 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Provencibacterium massiliense abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032527 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Provencibacterium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032528 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Providencia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032529 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Pseudomonadales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032530 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Pseudomonas aeruginosa abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032531 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Psychroserpens abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032532 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. QALR01 sp003150035 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032533 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Raoultella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032534 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. RC9 sp900317925 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032535 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Rhodanobacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032536 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Rhodococcus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032537 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Rhodovulum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032538 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Romboutsia ilealis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032539 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Roseibacillus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032540 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Rubneribacter sp002159915 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032541 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. RUG013 sp001486445 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032542 Genome-wide genotyping array 2022-02-01 34757267 Teng MS 2021-10-15 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/34757267 Genome-wide association study revealed novel candidate gene loci associated with soluble E-selectin levels in a Taiwanese population. Soluble E-selectin levels 4,525 East Asian ancestry individuals NA Affymetrix [7338548] (imputed) 4 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90093359 Genome-wide genotyping array 2022-02-01 34757267 Teng MS 2021-10-15 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/34757267 Genome-wide association study revealed novel candidate gene loci associated with soluble E-selectin levels in a Taiwanese population. Soluble E-selectin levels (adjusted for ABO rs2519093 genotypes) 4,525 East Asian ancestry individuals NA Affymetrix [7338548] (imputed) 6 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90093360 Genome-wide genotyping array 2022-04-29 35347246 Kimbrel NA 2022-03-28 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35347246 A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. Suicide attempts 9,196 European ancestry cases, 287,370 European ancestry controls up to 29,803 European ancestry cases, up to 522,363 European ancestry controls Affymetrix [NR] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90102464 Genome-wide genotyping array 2022-04-29 35347246 Kimbrel NA 2022-03-28 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35347246 A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. Suicide attempts 3,507 African American cases, 74,306 African American controls up to 29,803 African American cases, up to 522,363 African American controls Affymetrix [NR] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90102465 Genome-wide genotyping array 2022-04-29 35347246 Kimbrel NA 2022-03-28 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35347246 A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. Suicide attempts 1,271 Hispanics ancestry cases, 29,306 Hispanics ancestry controls NA Affymetrix [NR] (imputed) 3 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90102466 Genome-wide genotyping array 2022-04-29 35347246 Kimbrel NA 2022-03-28 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35347246 A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. Suicide attempts 115 Asian ancestry cases, 4,082 Asian ancestry controls NA Affymetrix [NR] (imputed) 3 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90102467 Genome-wide genotyping array 2022-04-29 35347246 Kimbrel NA 2022-03-28 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35347246 A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci. Suicide attempts 9,196 European ancestry cases, 287,370 European ancestry controls, 3,507 African American cases, 74,306 African American controls, 1,271 Hispanics ancestry cases, 29,306 Hispanics ancestry controls, 115 Asian ancestry cases, 4,082 Asian ancestry controls up to 29,803 African American, European cases, up to 522,363 African American, European controls Affymetrix [NR] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90102468 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133739 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133740 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133741 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133742 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133743 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-oleoyl-GPC (18:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133744 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-oleoyl-GPI (18:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133745 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-2-oleoyl-GPS (18:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133746 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 7-methylguanine levels in elite athletes 490 individuals NA Illumina [275016] 3 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90133747 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 7-methylxanthine levels in elite athletes 490 individuals NA Illumina [275016] 2 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90133748 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 9,10-DiHOME levels in elite athletes 490 individuals NA Illumina [275016] 2 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90133749 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-GPA (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133750 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-GPC (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 10 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133751 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-GPE (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133752 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-GPG (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133753 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Adenine levels in elite athletes 490 individuals NA Illumina [275016] 4 Adenine measurement http://www.ebi.ac.uk/efo/EFO_0021573 GCST90133754 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-GPI (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133755 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Adrenate (22:4n6) levels in elite athletes 490 individuals NA Illumina [275016] 2 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90133756 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-stearoyl-GPS (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133757 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Alanine levels in elite athletes 490 individuals NA Illumina [275016] 7 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90133758 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Allantoin levels in elite athletes 490 individuals NA Illumina [275016] 1 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90133759 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,2-dilinoleoyl-GPC (18:2/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133760 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,2-dipalmitoyl-GPC (16:0/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133761 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,2-dipalmitoyl-GPE (16:0/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 11 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133762 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 10-heptadecenoate (17:1n7) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133763 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Clostridium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093762 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Erysipelotrichaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093738 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Lactobacillaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093739 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Eubacteriaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093740 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Phascolarctobacterium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093768 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Ruminococcaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093742 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Enterobacteriaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093743 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Clostridiales_Family_XI_Incertae_Sedis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093744 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Anaerotruncus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093774 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Ruminococcus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093775 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Fusobacteriaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093746 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Campylobacteraceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093747 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Sutterellaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093748 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Bacillales_noname) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093749 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Oscillospiraceae) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093750 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Escherichia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093784 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Sutterella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093785 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Oxalobacteraceae) 614 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093752 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Verrucomicrobiaceae) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093753 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Aerococcaceae) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093754 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Staphylococcaceae) 603 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093755 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Neisseriaceae) 596 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093756 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Leuconostocaceae) 595 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093757 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Oribacterium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093758 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Dorea) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093759 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Burkholderia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093760 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Anaerostipes) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093761 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Bacteroidaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093737 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Dialister) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093763 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Fusobacterium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093764 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Collinsella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093765 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Blautia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093766 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Subdoligranulum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093767 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Streptococcaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093741 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Veillonella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093769 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Roseburia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093770 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Odoribacter) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093771 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Prevotella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093772 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Bacteroides) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093773 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Bifidobacteriaceae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093745 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Faecalibacterium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093776 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Alistipes) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093777 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Lactococcus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093778 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Porphyromonas) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093779 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Eggerthella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093780 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Streptococcus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093781 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Pseudoflavonifractor) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093782 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Enterococcus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093783 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (family Spirochaetaceae) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093751 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Coprococcus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093786 Genome-wide sequencing 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant GAG242N carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 1 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092542 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant GAG302K carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092543 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant GAG357S carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092544 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant GAG397R carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092545 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant GAG403K carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092546 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant POL432R carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092547 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant POL837I carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092548 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant NEF071K carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092549 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant NEF092R carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092550 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant NEF102H carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092551 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant NEF105R carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092552 Genome-wide genotyping array 2022-01-07 33974707 Gabrielaite M 2021-05-11 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/33974707 Human immunotypes impose selection on viral genotypes through viral epitope specificity. Viral variant NEF135F carrier status in HIV infection 21 Asian ancestry individuals, 432 African ancestry individuals, 382 Hispanic or Latin American individuals, 1,250 European ancestry individuals, 37 individuals NA Affymetrix [388501] 0 viral subtype carrier status http://www.ebi.ac.uk/efo/EFO_0010234 GCST90092553 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_finegoldii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093887 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_rectale) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093888 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_butyrate-producing_bacterium_SS3/4) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093889 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Roseburia_hominis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093890 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_plebeius) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093891 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Odoribacter_splanchnicus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093892 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Clostridiales_bacterium_1_7_47FAA) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093893 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_helcogenes) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093894 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Alistipes_sp__HGB5) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093895 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_eligens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093896 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Alistipes_putredinis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093897 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Butyrivibrio_crossotus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093898 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Clostridium_sp__D5) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093899 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Oribacterium_sinus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093900 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance ([Bacteroides]_pectinophilus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093901 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_ventriosum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093902 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_dorei) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093903 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance ([Ruminococcus]_torques) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093904 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_biforme) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093905 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_scindens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093906 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Marvinbryantia_formatexigens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093907 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance ([Ruminococcus]_gnavus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093908 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_fluxus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093909 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Dorea_longicatena) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093910 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Clostridium_sp__L2-50) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093911 Genome-wide sequencing 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-linoleoylglycerol (18:2) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133789 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-myristoylglycerol (14:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133790 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-oleoylglycerol (18:1) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133791 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-palmitoleoyl-GPC (16:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133792 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-palmitoleoylglycerol (16:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133793 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Carnitine levels in elite athletes 490 individuals NA Illumina [275016] 7 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90133806 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxybutyrylcarnitine (2) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133807 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-palmitoyl-GPC (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133794 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-palmitoylglycerol (16:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133795 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-stearoyl-GPE (18:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133796 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Biliverdin levels in elite athletes 490 individuals NA Illumina [275016] 2 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90133797 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. C-glycosyltryptophan levels in elite athletes 490 individuals NA Illumina [275016] 2 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90133798 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Caffeic acid sulfate levels in elite athletes 490 individuals NA Illumina [275016] 3 Caffeic acid measurement http://www.ebi.ac.uk/efo/EFO_0021578 GCST90133799 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Caffeine levels in elite athletes 490 individuals NA Illumina [275016] 9 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90133800 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Campesterol levels in elite athletes 490 individuals NA Illumina [275016] 5 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90133801 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 21-hydroxypregnenolone disulfate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133802 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxy-3-methylglutarate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133803 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxybutyrate (BHBA) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133804 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxybutyrylcarnitine (1) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133805 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxydecanoate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133808 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Catechol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 3 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90133809 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxyhexanoate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133810 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxylaurate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133811 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxymyristate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133812 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-hydroxyoctanoate levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133813 Genome-wide genotyping array 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Lachnospiraceae_bacterium_9_1_43BFAA) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093837 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Veillonella_parvula) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093838 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Veillonella_sp__oral_taxon_158) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093839 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_clarus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093840 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_dysgalactiae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093841 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_timonensis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093842 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_gallolyticus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093843 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_fragilis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093844 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_caccae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093845 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Blautia_hydrogenotrophica) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093846 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_dorei/vulgatus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093847 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_thetaiotaomicron) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093848 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Ruminococcaceae_bacterium_D16) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093849 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_anginosus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093850 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Subdoligranulum_variabile) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093851 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_cylindroides) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093852 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Ruminococcus_sp__5_1_39BFAA) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093853 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Anaerotruncus_colihominis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093854 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Holdemania_filiformis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093855 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Coprococcus_catus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093856 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Alistipes_shahii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093857 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_copri) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093858 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Pseudoflavonifractor_capillosus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093859 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_xylanisolvens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093860 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Erysipelotrichaceae_bacterium_5_2_54FAA) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093861 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_hallii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093912 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_infantis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093913 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Dialister_invisus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093914 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_saccharolyticum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093915 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_siraeum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093916 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_symbiosum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093917 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_intestinalis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093918 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Coprobacillus_sp__29_1) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093919 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Veillonella_dispar) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093920 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Lachnospiraceae_bacterium_3_1_57FAA_CT1) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093921 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Erysipelotrichaceae_bacterium_3_1_53) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093922 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (butyrate-producing_bacterium_SSC/2) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093923 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_stercoris) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093924 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_perfringens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093925 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Escherichia_coli) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093926 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eggerthella_lenta) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093927 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Haemophilus_parainfluenzae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093928 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Parabacteroides_merdae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093929 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Ruminococcus_sp__SR1/5) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093930 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_ovatus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093931 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Faecalibacterium_prausnitzii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093932 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_parasanguinis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093933 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_bolteae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093934 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Paraprevotella_xylaniphila) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093935 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_salanitronis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093936 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Clostridium_sp__HGF2) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093862 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_buccalis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093863 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Enterococcus_faecium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093864 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_oris) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093865 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Lachnospiraceae_bacterium_1_4_56FAA) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093866 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_methylpentosum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093867 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_ramosum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093868 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_salivarius) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093869 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance ([Ruminococcus]_obeum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093870 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Ruminococcus_bromii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093871 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Lachnospiraceae_bacterium_4_1_37FAA) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093872 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Capnocytophaga_sp__oral_taxon_329) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093873 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Roseburia_intestinalis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093874 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bilophila_wadsworthia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093875 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Ruminococcus_lactaris) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093876 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Dorea_formicigenerans) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093877 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (butyrate-producing_bacterium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093878 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Lactobacillus_ruminis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093879 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Phascolarctobacterium_succinatutens) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093880 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Eubacterium_limosum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093881 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Blautia_hansenii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093882 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bifidobacterium_longum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093883 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Streptococcus_thermophilus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093884 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Coprococcus_eutactus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093885 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Campylobacter_jejuni) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093886 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Treponema) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093812 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Acidaminococcus) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093813 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Tannerella) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093814 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Salmonella) 616 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093815 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Solobacterium) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093816 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Actinomyces) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093817 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Mitsuokella) 615 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093818 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Oxalobacter) 614 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093819 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Akkermansia) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093820 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Mobiluncus) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093821 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Anaerococcus) 613 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093822 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Abiotrophia) 609 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093823 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Aggregatibacter) 608 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093824 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Staphylococcus) 602 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093825 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Neisseria) 595 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093826 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Weissella) 587 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093827 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Prevotella_bivia) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093828 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Bacteroides_eggerthii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093829 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Parasutterella_excrementihominis) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093830 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Roseburia_inulinivorans) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093831 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance ([Clostridium]_difficile) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093832 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Clostridium_leptum) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093833 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (unclassified_Lachnospiraceae_bacterium_2_1_46FAA) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093834 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (Klebsiella_variicola/pneumoniae) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093835 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance ([Clostridium]_bartlettii) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093836 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Haemophilus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093787 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Butyrivibrio) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093788 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Eubacterium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093789 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Citrobacter) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093790 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Bifidobacterium) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093791 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Coprobacillus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093792 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Capnocytophaga) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093793 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Granulicatella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093794 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Bilophila) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093795 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Holdemania) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093796 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Megasphaera) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093797 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Peptoniphilus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093798 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Peptostreptococcus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093799 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Campylobacter) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093800 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Parabacteroides) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093801 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Paraprevotella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093802 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Enterobacter) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093803 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Klebsiella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093804 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Parasutterella) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093805 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Lactobacillus) 618 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093806 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Oscillibacter) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093807 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Anaerofustis) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093808 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Atopobium) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093809 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Gemella) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093810 Genome-wide sequencing 2022-02-21 33563976 Liu X 2021-02-09 Cell Discov www.ncbi.nlm.nih.gov/pubmed/33563976 A genome-wide association study for gut metagenome in Chinese adults illuminates complex diseases. Gut microbiota abundance (genus Desulfovibrio) 617 Chinese ancestry individuals 663 Chinese ancestry individuals NR [43342216] 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90093811 Genome-wide sequencing 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleoyl ethanolamide levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133989 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133990 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133991 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleoyl-linolenoyl-glycerol (18:2/18:3) [2] levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133992 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleoyl-linoleoyl-glycerol (18:2/18:2) [1] levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133993 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Lysine levels in elite athletes 490 individuals NA Illumina [275016] 3 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90133994 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Malate levels in elite athletes 490 individuals NA Illumina [275016] 2 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90133995 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Maleate levels in elite athletes 490 individuals NA Illumina [275016] 7 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90133996 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Maltose levels in elite athletes 490 individuals NA Illumina [275016] 1 Maltose measurement http://www.ebi.ac.uk/efo/EFO_0021649 GCST90133997 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleoylcarnitine (C18:2) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133998 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Mannose levels in elite athletes 490 individuals NA Illumina [275016] 3 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90133999 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Margarate (17:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90134000 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleoylcholine levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134001 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Margaroylcarnitine levels in elite athletes 490 individuals NA Illumina [275016] 11 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134002 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Methionine sulfoxide levels in elite athletes 490 individuals NA Illumina [275016] 5 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90134003 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Methionine levels in elite athletes 490 individuals NA Illumina [275016] 1 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90134004 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Myo-inositol levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134005 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Myristate (14:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134006 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Myristoleate (14:1n5) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134007 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Myristoleoylcarnitine (C14:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134008 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Myristoyl dihydrosphingomyelin (d18:0/14:0) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134009 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Myristoylcarnitine (C14) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134010 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-behenoyl-sphingadienine (d18:2/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134011 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-oleoylserine levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134012 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-oleoyltaurine levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134013 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isoleucine levels in elite athletes 490 individuals NA Illumina [275016] 4 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90133964 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133965 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isovalerate levels in elite athletes 490 individuals NA Illumina [275016] 6 isovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021051 GCST90133966 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133967 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Glycoursodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133968 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hexadecadienoate (16:2n6) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133969 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Kynurenine levels in elite athletes 490 individuals NA Illumina [275016] 5 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90133970 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hexanoylcarnitine (C6) levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133971 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hexanoylglutamine levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133972 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hexanoylglycine levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133973 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Hyocholate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133974 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Isoursodeoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133975 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Lactosyl-N-behenoyl-sphingosine (d18:1/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 12 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133976 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Leucine levels in elite athletes 490 individuals NA Illumina [275016] 7 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90133977 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) levels in elite athletes 490 individuals NA Illumina [275016] 9 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133978 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133979 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Laurate (12:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133980 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Laurylcarnitine (C12) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133981 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Leukotriene B4 levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133982 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Leukotriene B5 levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133983 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Von Willebrand factor levels or factor VIII levels or tissue plasminogen activator levels (pleiotropy) 32,610 European, African American, East Asian, South Asian or Hispanic individuals with factor VIII measurements, 26,929 European ancestry individuals with tPA measurements, 46,354 European, African American or Hispanic individuals with vWF measurements NA NR [NR] 0 factor VIII measurement, von Willebrand factor measurement, tissue plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0004630, http://www.ebi.ac.uk/efo/EFO_0004629, http://www.ebi.ac.uk/efo/EFO_0004791 GCST90129561 Genome-wide genotyping array 2022-07-20 35285134 Temprano-Sagrera G 2022-03-14 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/35285134 Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations. Venous thromboembolism or factor VII levels (pleiotropy) 27,495 European or African American individuals with measurements, 30,234 European or African American VTE cases, 172,122 European or African American VTE controls NA NR [NR] 28 venous thromboembolism, factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0004619 GCST90129535 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Lignoceroyl sphingomyelin (d18:1/24:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133984 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Lignoceroylcarnitine (C24) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133985 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linoleate (18:2n6) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133986 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linolenate [alpha or gamma; (18:3n3 or 6)] levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133987 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Linolenoylcarnitine (C18:3) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133988 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Trans-4-hydroxyproline levels in elite athletes 490 individuals NA Illumina [275016] 1 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133613 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Trans-urocanate levels in elite athletes 490 individuals NA Illumina [275016] 8 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133614 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Tyramine O-sulfate levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133615 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Urea levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133616 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Vanillactate levels in elite athletes 490 individuals NA Illumina [275016] 5 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133617 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Vanillic alcohol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 1 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133618 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Vanillylmandelate (VMA) levels in elite athletes 490 individuals NA Illumina [275016] 6 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90133619 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arabitol/xylitol levels in elite athletes 490 individuals NA Illumina [275016] 1 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133620 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arabonate/xylonate levels in elite athletes 490 individuals NA Illumina [275016] 3 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133621 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Galactonate levels in elite athletes 490 individuals NA Illumina [275016] 8 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133622 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Mannitol/sorbitol levels in elite athletes 490 individuals NA Illumina [275016] 4 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133623 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-aminobutyrate levels in elite athletes 490 individuals NA Illumina [275016] 4 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90133624 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylglucosamine/N-acetylgalactosamine levels in elite athletes 490 individuals NA Illumina [275016] 2 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133625 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N6-carboxymethyllysine levels in elite athletes 490 individuals NA Illumina [275016] 6 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133626 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ribitol levels in elite athletes 490 individuals NA Illumina [275016] 2 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133627 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ribonate levels in elite athletes 490 individuals NA Illumina [275016] 2 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133628 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sedoheptulose levels in elite athletes 490 individuals NA Illumina [275016] 2 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133629 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Xylose levels in elite athletes 490 individuals NA Illumina [275016] 2 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90133630 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-methylnicotinamide levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133631 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Alpha-CEHC sulfate levels in elite athletes 490 individuals NA Illumina [275016] 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133632 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxyglutarate levels in elite athletes 490 individuals NA Illumina [275016] 4 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90133633 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Bilirubin (Z,Z) levels in elite athletes 490 individuals NA Illumina [275016] 9 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133634 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-CEHC levels in elite athletes 490 individuals NA Illumina [275016] 3 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133635 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-tocopherol/beta-tocopherol levels in elite athletes 490 individuals NA Illumina [275016] 1 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133636 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxypalmitate levels in elite athletes 490 individuals NA Illumina [275016] 1 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90133637 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gulonate levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133638 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxystearate levels in elite athletes 490 individuals NA Illumina [275016] 6 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90133639 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Heme levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133640 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N1-Methyl-2-pyridone-5-carboxamide levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133641 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N1-Methyl-4-pyridone-3-carboxamide levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133642 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Nicotinamide levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133643 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pyridoxal levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133644 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Quinolinate levels in elite athletes 490 individuals NA Illumina [275016] 3 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133645 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Retinol (Vitamin A) levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133646 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Trigonelline (N'-methylnicotinate) levels in elite athletes 490 individuals NA Illumina [275016] 3 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133647 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-methylcitrate/homocitrate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133648 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Aconitate [cis or trans] levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133649 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Alpha-ketoglutarate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133650 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Citraconate/glutaconate levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90133651 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-oleoyl)-GPE (P-18:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133652 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133653 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133654 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133655 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133656 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133657 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133658 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133659 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133660 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-palmitoyl)-GPC (P-16:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133661 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133663 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3alpha,17alpha-diol monosulfate levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133839 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Deoxycholate levels in elite athletes 490 individuals NA Illumina [275016] 3 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90133840 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3alpha,17beta-diol disulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133841 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133842 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dihomo-linoleate (20:2n6) levels in elite athletes 490 individuals NA Illumina [275016] 3 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90133843 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133844 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3beta,17alpha-diol disulfate levels in elite athletes 490 individuals NA Illumina [275016] 8 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133845 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133846 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-pregnan-3(alpha or beta),20beta-diol disulfate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133847 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-pregnan-3beta-ol,20-one sulfate levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133848 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-pregnan-3beta,20alpha-diol disulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133849 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 25 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133850 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels in elite athletes 490 individuals NA Illumina [275016] 10 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133851 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dimethylglycine levels in elite athletes 490 individuals NA Illumina [275016] 7 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90133852 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-Hoca) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133853 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Acetylcarnitine (C2) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133854 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Adipoylcarnitine (C6-DC) levels in elite athletes 490 individuals NA Illumina [275016] 10 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133855 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Adrenoylcarnitine (C22:4) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133856 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Andro steroid monosulfate C19H28O6S (1) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133857 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Androstenediol (3alpha, 17alpha) monosulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 9 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133858 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dodecanedioate levels in elite athletes 490 individuals NA Illumina [275016] 7 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90133859 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Androstenediol (3alpha, 17alpha) monosulfate (3) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133860 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. DSGEGDFXAEGGGVR levels in elite athletes 490 individuals NA Illumina [275016] 3 DSGEGDFXAEGGGVR measurement http://www.ebi.ac.uk/efo/EFO_0021136 GCST90133861 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Androstenediol (3beta,17beta) disulfate (1) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133862 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Androstenediol (3beta,17beta) disulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133863 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Eicosapentaenoate (EPA; 20:5n3) levels in elite athletes 490 individuals NA Illumina [275016] 6 eicosapentaenoate EPA; 20:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021049 GCST90133864 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Androstenediol (3beta,17beta) monosulfate (1) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133865 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Androstenediol (3beta,17beta) monosulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133866 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Epiandrosterone sulfate levels in elite athletes 490 individuals NA Illumina [275016] 10 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90133867 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ergothioneine levels in elite athletes 490 individuals NA Illumina [275016] 10 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90133868 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arachidate (20:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133869 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Erythritol levels in elite athletes 490 individuals NA Illumina [275016] 5 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90133870 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Erythronate levels in elite athletes 490 individuals NA Illumina [275016] 3 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90133871 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ethylmalonate levels in elite athletes 490 individuals NA Illumina [275016] 9 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90133872 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arachidonate (20:4n6) levels in elite athletes 490 individuals NA Illumina [275016] 2 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133873 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arachidonoylcarnitine (C20:4) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133874 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Arachidonoylcholine levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133875 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Fructose levels in elite athletes 490 individuals NA Illumina [275016] 8 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90133876 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Fumarate levels in elite athletes 490 individuals NA Illumina [275016] 1 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90133877 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Azelate (nonanedioate) levels in elite athletes 490 individuals NA Illumina [275016] 7 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133878 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Behenoyl dihydrosphingomyelin (d18:0/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133879 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Behenoyl sphingomyelin (d18:1/22:0) levels in elite athletes 490 individuals NA Illumina [275016] 5 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133880 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Behenoylcarnitine (C22) levels in elite athletes 490 individuals NA Illumina [275016] 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133881 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Beta-sitosterol levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133882 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Caprate (10:0) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133883 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylglutamate levels in elite athletes 490 individuals NA Illumina [275016] 8 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90133884 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylglutamine levels in elite athletes 490 individuals NA Illumina [275016] 10 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90133885 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Caproate (6:0) levels in elite athletes 490 individuals NA Illumina [275016] 3 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133886 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Caprylate (8:0) levels in elite athletes 490 individuals NA Illumina [275016] 4 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90133887 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylisoleucine levels in elite athletes 490 individuals NA Illumina [275016] 4 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90133888 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Ximenoylcarnitine (C26:1) levels in elite athletes 490 individuals NA Illumina [275016] 6 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90134114 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Phenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 6 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90134115 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Phenylacetate levels in elite athletes 490 individuals NA Illumina [275016] 6 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90134116 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2'-deoxyinosine levels in elite athletes 490 individuals NA Illumina [275016] 2 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134117 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Phenylacetylglutamine levels in elite athletes 490 individuals NA Illumina [275016] 7 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90134118 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Phenylalanine levels in elite athletes 490 individuals NA Illumina [275016] 2 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90134119 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Phenyllactate (PLA) levels in elite athletes 490 individuals NA Illumina [275016] 8 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90134120 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Phosphate levels in elite athletes 490 individuals NA Illumina [275016] 2 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90134121 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2'-deoxyuridine levels in elite athletes 490 individuals NA Illumina [275016] 8 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134122 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pipecolate levels in elite athletes 490 individuals NA Illumina [275016] 8 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90134123 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2'-O-methyluridine levels in elite athletes 490 individuals NA Illumina [275016] 7 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134124 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 5,6-dihydrothymine levels in elite athletes 490 individuals NA Illumina [275016] 2 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134125 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Beta-alanine levels in elite athletes 490 individuals NA Illumina [275016] 3 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134126 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Cytidine levels in elite athletes 490 individuals NA Illumina [275016] 2 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134127 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Dihydroorotate levels in elite athletes 490 individuals NA Illumina [275016] 4 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134128 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pro-hydroxy-pro levels in elite athletes 490 individuals NA Illumina [275016] 10 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90134129 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Proline levels in elite athletes 490 individuals NA Illumina [275016] 2 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90134130 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N1-methylinosine levels in elite athletes 490 individuals NA Illumina [275016] 10 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134131 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N6-carbamoylthreonyladenosine levels in elite athletes 490 individuals NA Illumina [275016] 6 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134132 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Orotate levels in elite athletes 490 individuals NA Illumina [275016] 4 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134133 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pseudouridine levels in elite athletes 490 individuals NA Illumina [275016] 1 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90134134 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Orotidine levels in elite athletes 490 individuals NA Illumina [275016] 6 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134135 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pyridoxate levels in elite athletes 490 individuals NA Illumina [275016] 13 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90134136 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pyroglutamine levels in elite athletes 490 individuals NA Illumina [275016] 9 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST90134137 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Uracil levels in elite athletes 490 individuals NA Illumina [275016] 3 nucleotide measurement http://www.ebi.ac.uk/efo/EFO_0010513 GCST90134138 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Pyruvate levels in elite athletes 490 individuals NA Illumina [275016] 5 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90134139 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Quinate levels in elite athletes 490 individuals NA Illumina [275016] 12 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90134140 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 4-hydroxyphenylacetylglutamine levels in elite athletes 490 individuals NA Illumina [275016] 4 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134141 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamyl-2-aminobutyrate levels in elite athletes 490 individuals NA Illumina [275016] 2 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134142 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamyl-alpha-lysine levels in elite athletes 490 individuals NA Illumina [275016] 5 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134143 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamyl-epsilon-lysine levels in elite athletes 490 individuals NA Illumina [275016] 5 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134144 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylalanine levels in elite athletes 490 individuals NA Illumina [275016] 3 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134145 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylglycine levels in elite athletes 490 individuals NA Illumina [275016] 5 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134146 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. S-adenosylhomocysteine (SAH) levels in elite athletes 490 individuals NA Illumina [275016] 5 S-adenosylhomocysteine measurement http://www.ebi.ac.uk/efo/EFO_0010531 GCST90134147 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamylhistidine levels in elite athletes 490 individuals NA Illumina [275016] 4 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134148 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Gamma-glutamyltryptophan levels in elite athletes 490 individuals NA Illumina [275016] 3 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134149 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Histidylalanine levels in elite athletes 490 individuals NA Illumina [275016] 9 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134150 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Salicylate levels in elite athletes 490 individuals NA Illumina [275016] 7 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90134151 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Sarcosine levels in elite athletes 490 individuals NA Illumina [275016] 8 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90134152 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Leucylalanine levels in elite athletes 490 individuals NA Illumina [275016] 7 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134153 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Leucylglycine levels in elite athletes 490 individuals NA Illumina [275016] 11 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134154 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Serine levels in elite athletes 490 individuals NA Illumina [275016] 5 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90134155 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Serotonin levels in elite athletes 490 individuals NA Illumina [275016] 4 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90134156 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. N-acetylcarnosine levels in elite athletes 490 individuals NA Illumina [275016] 4 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134157 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Phenylacetylglutamate levels in elite athletes 490 individuals NA Illumina [275016] 3 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134158 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Prolylglycine levels in elite athletes 490 individuals NA Illumina [275016] 6 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134159 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Threonylphenylalanine levels in elite athletes 490 individuals NA Illumina [275016] 2 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134160 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Valylglutamine levels in elite athletes 490 individuals NA Illumina [275016] 2 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134161 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Valylglycine levels in elite athletes 490 individuals NA Illumina [275016] 3 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134162 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. Valylleucine levels in elite athletes 490 individuals NA Illumina [275016] 3 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90134163 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,3-dimethylurate levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134165 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-aminophenol sulfate levels in elite athletes 490 individuals NA Illumina [275016] 7 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134166 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-hydroxyhippurate (salicylurate) levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134167 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-(3-hydroxyphenyl)propionate sulfate levels in elite athletes 490 individuals NA Illumina [275016] 5 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134171 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 1,2,3-benzenetriol sulfate (2) levels in elite athletes 490 individuals NA Illumina [275016] 6 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134164 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-oxindole-3-acetate levels in elite athletes 490 individuals NA Illumina [275016] 2 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134168 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2-piperidinone levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134169 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 2,3-dihydroxyisovalerate levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134170 Genome-wide genotyping array 2022-09-01 31882771 Al-Khelaifi F 2019-12-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31882771 Metabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance. 3-(3-hydroxyphenyl)propionate levels in elite athletes 490 individuals NA Illumina [275016] 4 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST90134172 Genome-wide genotyping array 2022-01-12 34927100 Stuart PE 2021-11-06 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34927100 Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide. Psoriasis 2,590 South Asian ancestry cases, 1,720 South Asian ancestry controls NA Illumina [9200335] (imputed) 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90019015 Genome-wide genotyping array 2022-01-12 34927100 Stuart PE 2021-11-06 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34927100 Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide. Psoriasis 15,967 European ancestry cases, 28,194 European ancestry controls NA Affymetrix, Illumina, Perlegen [9010555] (imputed) 2 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90019016 Genome-wide genotyping array, Targeted genotyping array [Targeted array = Immunochip] 2022-01-12 34927100 Stuart PE 2021-11-06 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34927100 Transethnic analysis of psoriasis susceptibility in South Asians and Europeans enhances fine-mapping in the MHC and genomewide. Psoriasis 15,967 European ancestry cases, 28,194 European ancestry controls, 2,590 South Asian ancestry cases, 1,720 South Asian ancestry controls NA Affymetrix, Illumina, Perlegen [8942692] (imputed) 2 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90019017 Genome-wide genotyping array, Targeted genotyping array [Targeted array = Immunochip] 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Citrobacter A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032320 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032321 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium E sporosphaeroides abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032322 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium I abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032323 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium M clostridioforme abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032324 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium M sp001304855 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032325 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium P abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032326 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium saudiense abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032327 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium S felsineum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032328 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Clostridium tertium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032329 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Collinsella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032330 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Comamonas B abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032331 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Comamonas abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032332 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Coprobacillus cateniformis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032333 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Coprobacillus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032334 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Coprobacter secundus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032335 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Corynebacterium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032336 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Cyanobacteria abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032337 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Demequinaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032338 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Demequina abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032339 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Desulfobacterota A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032340 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Desulfovibrionaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032341 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Desulfovibrionales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032342 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Desulfovibrionia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032343 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Desulfovibrio piger abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032344 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eubacterium callanderi abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032371 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eubacterium F sp000434115 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032372 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ezakiellaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032377 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. F0428 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032378 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalibacterium sp002160895 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032380 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicatena sp002397985 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032386 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fibrobacteria abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032394 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Escherichia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032370 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eubacterium I ramulus A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032373 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eubacterium Q abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032374 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eubacterium R coprostanoligenes abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032375 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eubacterium R sp000431535 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032376 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalibacterium prausnitzii E abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032379 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicatena glycyrrhizinilyticum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032381 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicatena lactaris abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032382 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicatena sp000364245 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032383 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicatena sp001517425 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032384 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicatena sp002161355 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032385 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicatena torques abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032387 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicoccus pleomorphus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032388 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalicoccus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032389 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Faecalitalea cylindroides abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032390 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fervidobacteriaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032391 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fibrobacteraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032392 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fibrobacterales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032393 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-698 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032295 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-776 sp000438195 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032296 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-776 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032297 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-81 sp000435795 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032298 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-822 sp000432855 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032299 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-822 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032300 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-826 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032301 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-83 sp000435555 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032302 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-83 sp002392625 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032303 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-841 sp002479075 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032304 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-873 sp001701165 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032305 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-877 sp000433455 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032306 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-877 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032307 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-882 sp003486385 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032308 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-884 sp000433875 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032309 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-884 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032310 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-977 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032311 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Caloranaerobacteraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032312 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Caloranaerobacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032313 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Campylobacter D abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032314 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Cetobacterium A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032315 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CHKCI006 sp900018345 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032316 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Chloroflexales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032317 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Chromatiales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032318 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Chromobacteriaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032319 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-273 sp003534295 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032270 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-274 sp000432155 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032271 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-302 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032272 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-345 sp000433315 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032273 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-345 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032274 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-349 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032275 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-390 sp003523225 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032276 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-433 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032277 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-448 sp000433415 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032278 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-448 sp003150135 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032279 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-448 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032280 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-449 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032281 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-452 sp000434035 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032282 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-452 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032283 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-465 sp000433135 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032284 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-475 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032285 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-485 sp002362485 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032286 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-485 sp002404675 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032287 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-488 sp000434055 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032288 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-488 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032289 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-495 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032290 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-510 sp002432425 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032291 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-552 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032292 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-590 sp000431135 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032293 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-632 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032294 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Brevibacillaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032245 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Brevibacillales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032246 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Brevibacillus B abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032247 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Butyricimonas sp900258545 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032248 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-1000 sp000434555 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032249 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-1000 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032250 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-1031 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032251 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-110 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032252 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-145 sp000435615 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032253 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-145 sp002320005 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032254 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-145 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032255 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-170 sp003516765 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032256 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-177 sp002438685 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032257 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-177 sp002451755 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032258 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-177 sp003514385 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032259 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-177 sp003538135 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032260 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-177 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032261 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-180 sp000432435 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032262 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-194 sp002441865 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032263 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-245 sp000435175 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032264 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-245 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032265 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-269 sp001915995 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032266 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-269 sp001916065 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032267 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-269 sp002372935 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032268 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. CAG-273 sp003507395 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032269 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fimbriimonadia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032395 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Firmicutes A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032396 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Firmicutes E abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032397 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Firmicutes I abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032398 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Flavobacteriales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032399 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Flavonifractor sp002159265 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032400 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Flavonifractor sp900199495 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032401 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fournierella massiliensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032402 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Francisellaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032403 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Francisellales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032404 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. GCA-900066495 sp900066495 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032408 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. GCA-900066495 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032409 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. GCA-900066575 sp900066385 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032410 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. GCA-900066755 sp900066755 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032411 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. GCA-900199385 sp900320755 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032413 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Geminocystis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032414 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mebeverine (UKB data field 20003_1140879428) 2,246 European ancestry cases, 454,030 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042176 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - domperidone (UKB data field 20003_1140879430) 901 European ancestry cases, 455,375 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042177 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - loperamide (UKB data field 20003_1140879464) 1,479 European ancestry cases, 454,797 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042178 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - metoclopramide (UKB data field 20003_1140879494) 531 European ancestry cases, 455,745 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042179 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - fluoxetine (UKB data field 20003_1140879540) 5,300 European ancestry cases, 450,976 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042180 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amitriptyline (UKB data field 20003_1140879616) 8,612 European ancestry cases, 447,664 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042181 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - clomipramine (UKB data field 20003_1140879620) 299 European ancestry cases, 455,977 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042182 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dothiepin (UKB data field 20003_1140879628) 166 European ancestry cases, 456,110 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042183 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - imipramine (UKB data field 20003_1140879630) 235 European ancestry cases, 456,041 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042184 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - trazodone (UKB data field 20003_1140879634) 641 European ancestry cases, 455,635 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042185 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amantadine (UKB data field 20003_1140879644) 128 European ancestry cases, 456,148 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042186 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - chlorpromazine (UKB data field 20003_1140879658) 150 European ancestry cases, 456,126 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042187 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bisoprolol (UKB data field 20003_1140879760) 6,688 European ancestry cases, 449,588 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042188 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - celiprolol (UKB data field 20003_1140879762) 114 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042189 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - alfuzosin (UKB data field 20003_1140879774) 1,000 European ancestry cases, 207,768 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042190 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - doxazosin (UKB data field 20003_1140879778) 5,096 European ancestry cases, 451,180 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042191 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - indoramin (UKB data field 20003_1140879782) 109 European ancestry cases, 208,659 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042192 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - terbutaline (UKB data field 20003_1140879792) 676 European ancestry cases, 455,600 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042193 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - terazosin (UKB data field 20003_1140879798) 157 European ancestry cases, 456,119 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042194 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amlodipine (UKB data field 20003_1140879802) 18,435 European ancestry cases, 437,841 European ancestry controls NA NR [11842647] (imputed) 2 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042195 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for reducing amount of alcohol drunk: Health precaution (UKB data field 2664_3) 55,353 European ancestry cases, 114,477 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043656 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for reducing amount of alcohol drunk: Financial reasons (UKB data field 2664_4) 8,952 European ancestry cases, 160,878 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043657 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Reason for reducing amount of alcohol drunk: Other reason (UKB data field 2664_5) 89,574 European ancestry cases, 80,256 European ancestry controls NA NR [11842647] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90043658 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Proteinuria (PheCode 269) 114 European ancestry cases, 456,234 European ancestry controls NA NR [11842647] (imputed) 0 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90043659 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Paraproteinemia (PheCode 270.32) 103 European ancestry cases, 456,245 European ancestry controls NA NR [11842647] (imputed) 0 Paraproteinemia http://purl.obolibrary.org/obo/HP_0031047 GCST90043660 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hypertension 28,391 European ancestry cases, 28,246 European ancestry controls NA Affymetrix [15166444] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90086088 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hypertension 28,391 European ancestry cases, 28,246 European ancestry controls NA Affymetrix [12143829] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90086089 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hypertension 28,391 European ancestry cases, 28,246 European ancestry controls NA Affymetrix [15203319] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90086090 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hypertension 28,391 European ancestry cases, 28,246 European ancestry controls NA Affymetrix [11448799] (imputed) 1 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90086091 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Hypertension 28,391 European ancestry cases, 28,246 European ancestry controls NA Affymetrix [15650645] (imputed) 9 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90086092 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Frequent insomnia symptoms 3,972 European ancestry cases, 52,665 European ancestry controls NA Affymetrix [15036946] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90086093 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Frequent insomnia symptoms 3,972 European ancestry cases, 52,665 European ancestry controls NA Affymetrix [12096393] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90086094 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Frequent insomnia symptoms 3,972 European ancestry cases, 52,665 European ancestry controls NA Affymetrix [15073477] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90086095 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Frequent insomnia symptoms 3,972 European ancestry cases, 52,665 European ancestry controls NA Affymetrix [11401830] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90086096 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Frequent insomnia symptoms 3,972 European ancestry cases, 52,665 European ancestry controls NA Affymetrix [15514619] (imputed) 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90086097 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Iron deficiency 2,439 European ancestry cases, 54,198 European ancestry controls NA Affymetrix [14912767] (imputed) 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90086098 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Iron deficiency 2,439 European ancestry cases, 54,198 European ancestry controls NA Affymetrix [12025389] (imputed) 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90086099 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Iron deficiency 2,439 European ancestry cases, 54,198 European ancestry controls NA Affymetrix [14949278] (imputed) 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90086100 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Iron deficiency 2,439 European ancestry cases, 54,198 European ancestry controls NA Affymetrix [11349361] (imputed) 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90086101 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Iron deficiency 2,439 European ancestry cases, 54,198 European ancestry controls NA Affymetrix [15386714] (imputed) 1 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90086102 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Irritable bowel syndrome 3,117 European ancestry cases, 53,520 European ancestry controls NA Affymetrix [14973239] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90086103 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Irritable bowel syndrome 3,117 European ancestry cases, 53,520 European ancestry controls NA Affymetrix [12063777] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90086104 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Irritable bowel syndrome 3,117 European ancestry cases, 53,520 European ancestry controls NA Affymetrix [15009414] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90086105 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Irritable bowel syndrome 3,117 European ancestry cases, 53,520 European ancestry controls NA Affymetrix [11377101] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90086106 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Irritable bowel syndrome 3,117 European ancestry cases, 53,520 European ancestry controls NA Affymetrix [15448493] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90086107 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Age-related macular degeneration 3,685 European ancestry cases, 52,952 European ancestry controls NA Affymetrix [14904084] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90086108 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Age-related macular degeneration 3,685 European ancestry cases, 52,952 European ancestry controls NA Affymetrix [12048874] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90086109 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Age-related macular degeneration 3,685 European ancestry cases, 52,952 European ancestry controls NA Affymetrix [14938594] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90086110 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Age-related macular degeneration 3,685 European ancestry cases, 52,952 European ancestry controls NA Affymetrix [11380139] (imputed) 1 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90086111 Genome-wide genotyping array 2021-11-29 33893285 Guindo-Martinez M 2021-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33893285 The impact of non-additive genetic associations on age-related complex diseases. Age-related macular degeneration 3,685 European ancestry cases, 52,952 European ancestry controls NA Affymetrix [15377238] (imputed) 4 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90086112 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Methods of self-harm used: Stopping prescribed medication (UKB data field 20553_3) 329 European ancestry cases, 147,004 European ancestry controls NA NR [11842647] (imputed) 0 Self-injurious behavior, medication adherence behavior http://purl.obolibrary.org/obo/HP_0100716, http://www.ebi.ac.uk/efo/EFO_0006344 GCST90042851 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Methods of self-harm used: Ingesting a medication in excess of the normal dose (UKB data field 20553_4) 3,671 European ancestry cases, 143,662 European ancestry controls NA NR [11842647] (imputed) 0 Self-injurious behavior, medication adherence behavior http://purl.obolibrary.org/obo/HP_0100716, http://www.ebi.ac.uk/efo/EFO_0006344 GCST90042852 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Methods of self-harm used: Self-injury such as self-cutting, scratching or hitting, etc. (UKB data field 20553_5) 3,175 European ancestry cases, 144,158 European ancestry controls NA NR [11842647] (imputed) 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90042853 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Methods of self-harm used: Ingesting alcohol or a recreational or illicit drug (UKB data field 20553_6) 970 European ancestry cases, 146,363 European ancestry controls NA NR [11842647] (imputed) 0 drug misuse, Self-injurious behavior, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0011049, http://purl.obolibrary.org/obo/HP_0100716, http://www.ebi.ac.uk/efo/EFO_0004329 GCST90042854 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Actions taken following self-harm: See anyone from psychiatric or mental health services, including liaison services (UKB data field 20554_1) 2,102 European ancestry cases, 145,231 European ancestry controls NA NR [11842647] (imputed) 0 treatment, Self-injurious behavior http://www.ebi.ac.uk/efo/EFO_0000727, http://purl.obolibrary.org/obo/HP_0100716 GCST90042855 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Actions taken following self-harm: Need hospital treatment (eg A&E) (UKB data field 20554_3) 2,646 European ancestry cases, 144,687 European ancestry controls NA NR [11842647] (imputed) 0 treatment, Self-injurious behavior http://www.ebi.ac.uk/efo/EFO_0000727, http://purl.obolibrary.org/obo/HP_0100716 GCST90042856 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Actions taken following self-harm: Use a helpline / voluntary organization (UKB data field 20554_4) 623 European ancestry cases, 146,710 European ancestry controls NA NR [11842647] (imputed) 0 treatment, Self-injurious behavior http://www.ebi.ac.uk/efo/EFO_0000727, http://purl.obolibrary.org/obo/HP_0100716 GCST90042857 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Actions taken following self-harm: See own GP (UKB data field 20554_5) 1,537 European ancestry cases, 145,796 European ancestry controls NA NR [11842647] (imputed) 0 treatment, Self-injurious behavior http://www.ebi.ac.uk/efo/EFO_0000727, http://purl.obolibrary.org/obo/HP_0100716 GCST90042858 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Actions taken following self-harm: Receive help from friends / family / neighbours (UKB data field 20554_6) 1,826 European ancestry cases, 145,507 European ancestry controls NA NR [11842647] (imputed) 0 treatment, Self-injurious behavior http://www.ebi.ac.uk/efo/EFO_0000727, http://purl.obolibrary.org/obo/HP_0100716 GCST90042859 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of colon (PheCode 208) 19,026 European ancestry cases, 437,322 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90042860 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Seen doctor for nerves anxiety tension or depression (UKB data field 2090) 156,442 European ancestry cases, 296,621 European ancestry controls NA NR [11842647] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90042861 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Seen psychiatrist for nerves anxiety tension or depression (UKB data field 2100) 52,417 European ancestry cases, 401,764 European ancestry controls NA NR [11842647] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90042862 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of lip, oral cavity, and pharynx (PheCode 210) 988 European ancestry cases, 455,360 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90042863 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of other parts of digestive system (PheCode 211) 2,863 European ancestry cases, 453,485 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90042864 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of respiratory and intrathoracic organs (PheCode 212) 349 European ancestry cases, 455,999 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system neoplasm http://www.ebi.ac.uk/efo/EFO_0003853 GCST90042865 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of bone and articular cartilage (PheCode 213) 298 European ancestry cases, 456,050 European ancestry controls NA NR [11842647] (imputed) 0 bone neoplasm http://www.ebi.ac.uk/efo/EFO_0003820 GCST90042866 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Lipoma of skin and subcutaneous tissue (PheCode 214.1) 5,217 European ancestry cases, 451,131 European ancestry controls NA NR [11842647] (imputed) 0 lipoma http://www.ebi.ac.uk/efo/EFO_0000759 GCST90042867 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Lipoma (PheCode 214) 655 European ancestry cases, 455,693 European ancestry controls NA NR [11842647] (imputed) 0 lipoma http://www.ebi.ac.uk/efo/EFO_0000759 GCST90042868 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other benign neoplasm of connective and other soft tissue (PheCode 215) 1,023 European ancestry cases, 455,325 European ancestry controls NA NR [11842647] (imputed) 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90042869 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of skin (PheCode 216) 8,416 European ancestry cases, 447,932 European ancestry controls NA NR [11842647] (imputed) 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90042870 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nevus, non-neoplastic (PheCode 217.1) 351 European ancestry cases, 455,997 European ancestry controls NA NR [11842647] (imputed) 0 nevus http://www.ebi.ac.uk/efo/EFO_0000625 GCST90042871 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Uterine leiomyoma (PheCode 218.1) 7,187 European ancestry cases, 240,353 European ancestry controls NA NR [11842647] (imputed) 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90042872 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other benign neoplasm of uterus (PheCode 218.2) 225 European ancestry cases, 247,315 European ancestry controls NA NR [11842647] (imputed) 0 uterine neoplasm http://www.ebi.ac.uk/efo/EFO_0003859 GCST90042873 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Long standing illness disability or infirmity (UKB data field 2188) 145,122 European ancestry cases, 300,357 European ancestry controls NA NR [11842647] (imputed) 0 chronic disease http://www.ebi.ac.uk/efo/EFO_0009714 GCST90042874 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Wears glasses or contact lenses (UKB data field 2207) 405,672 European ancestry cases, 49,982 European ancestry controls NA NR [11842647] (imputed) 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90042875 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Number of things worried about during worst period of anxiety - One thing (UKB data field 20543) 25,093 European ancestry cases, 19,455 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90042826 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substances taken for depression: Unprescribed medication (more than once) (UKB data field 20546_1) 5,170 European ancestry cases, 142,226 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, clinical treatment http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042827 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substances taken for depression: Medication prescribed to you (for at least two weeks) (UKB data field 20546_3) 35,503 European ancestry cases, 111,893 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, clinical treatment http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042828 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substances taken for depression: Drugs or alcohol (more than once) (UKB data field 20546_4) 10,704 European ancestry cases, 136,692 European ancestry controls NA NR [11842647] (imputed) 0 drug misuse, unipolar depression, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0011049, http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004329 GCST90042829 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Activities undertaken to treat depression: Talking therapies, such as psychotherapy, counselling, group therapy or CBT (UKB data field 20547_1) 32,700 European ancestry cases, 114,696 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, treatment http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000727 GCST90042830 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Activities undertaken to treat depression: Other therapeutic activities such as mindfulness, yoga or art classes (UKB data field 20547_3) 11,705 European ancestry cases, 135,691 European ancestry controls NA NR [11842647] (imputed) 0 unipolar depression, treatment http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000727 GCST90042831 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: I was more talkative than usual (UKB data field 20548_1) 6,963 European ancestry cases, 136,228 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042832 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: I was more restless than usual (UKB data field 20548_2) 16,257 European ancestry cases, 126,934 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042833 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: My thoughts were racing (UKB data field 20548_3) 13,405 European ancestry cases, 129,786 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042834 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: I needed less sleep than usual (UKB data field 20548_5) 4,878 European ancestry cases, 138,313 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042835 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: I was more creative or had more ideas than usual (UKB data field 20548_6) 3,960 European ancestry cases, 139,231 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042836 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: I was easily distracted (UKB data field 20548_7) 11,685 European ancestry cases, 131,506 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042837 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: I was more confident than usual (UKB data field 20548_8) 4,196 European ancestry cases, 138,995 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042838 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manifestations of mania or irritability: I was more active than usual (UKB data field 20548_9) 7,286 European ancestry cases, 135,905 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement, irritability measurement http://www.ebi.ac.uk/efo/EFO_0007705, http://www.ebi.ac.uk/efo/EFO_0009594 GCST90042839 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substances taken for anxiety: Unprescribed medication (more than once) (UKB data field 20549_1) 3,233 European ancestry cases, 120,590 European ancestry controls NA NR [11842647] (imputed) 0 anxiety, clinical treatment http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042840 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substances taken for anxiety: Medication prescribed to you (for at least two weeks) (UKB data field 20549_3) 16,139 European ancestry cases, 107,684 European ancestry controls NA NR [11842647] (imputed) 0 anxiety, clinical treatment http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042841 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substances taken for anxiety: Drugs or alcohol (more than once) (UKB data field 20549_4) 6,726 European ancestry cases, 117,097 European ancestry controls NA NR [11842647] (imputed) 0 drug misuse, anxiety, alcohol drinking http://www.ebi.ac.uk/efo/EFO_0011049, http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004329 GCST90042842 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Activities undertaken to treat anxiety: Talking therapies, such as psychotherapy, counselling, group therapy or CBT (UKB data field 20550_1) 16,124 European ancestry cases, 107,699 European ancestry controls NA NR [11842647] (imputed) 0 anxiety, treatment http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0000727 GCST90042843 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Activities undertaken to treat anxiety: Other therapeutic activities such as mindfulness, yoga or art classes (UKB data field 20550_3) 7,213 European ancestry cases, 116,610 European ancestry controls NA NR [11842647] (imputed) 0 anxiety, treatment http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0000727 GCST90042844 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substance of prescription or over-the-counter medication addiction: A sedative, benzodiazepine or sleeping tablet (UKB data field 20551_1) 558 European ancestry cases, 145,548 European ancestry controls NA NR [11842647] (imputed) 0 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90042845 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substance of prescription or over-the-counter medication addiction: A painkiller (UKB data field 20551_2) 501 European ancestry cases, 145,605 European ancestry controls NA NR [11842647] (imputed) 0 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90042846 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Substance of prescription or over-the-counter medication addiction: Something else (UKB data field 20551_3) 280 European ancestry cases, 145,826 European ancestry controls NA NR [11842647] (imputed) 0 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90042847 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behavioural and miscellaneous addictions: Something else not mentioned (UKB data field 20552_1) 576 European ancestry cases, 145,530 European ancestry controls NA NR [11842647] (imputed) 0 addictive behaviour http://www.ebi.ac.uk/efo/EFO_0004347 GCST90042848 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Behavioural and miscellaneous addictions: A behaviour (UKB data field 20552_2) 1,535 European ancestry cases, 144,571 European ancestry controls NA NR [11842647] (imputed) 0 addictive behaviour http://www.ebi.ac.uk/efo/EFO_0004347 GCST90042849 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Methods of self-harm used: Something not listed (UKB data field 20553_1) 601 European ancestry cases, 146,732 European ancestry controls NA NR [11842647] (imputed) 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90042850 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of ovary (PheCode 220) 1,263 European ancestry cases, 246,277 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90042876 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of other female genital organs (PheCode 221) 171 European ancestry cases, 247,369 European ancestry controls NA NR [11842647] (imputed) 0 Genital neoplasm, female http://www.ebi.ac.uk/efo/EFO_1001331 GCST90042877 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other eye problems (UKB data field 2227) 65,649 European ancestry cases, 389,331 European ancestry controls NA NR [11842647] (imputed) 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90042878 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of male genital organs (PheCode 222) 129 European ancestry cases, 208,679 European ancestry controls NA NR [11842647] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90042879 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of kidney and other urinary organs (PheCode 223) 168 European ancestry cases, 456,180 European ancestry controls NA NR [11842647] (imputed) 0 urogenital neoplasm http://www.ebi.ac.uk/efo/EFO_0003863 GCST90042880 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hearing difficulty/problems: No (UKB data field 2247_0) 323,343 European ancestry cases, 114,424 European ancestry controls NA NR [11842647] (imputed) 4 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90042881 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hearing difficulty/problems: Yes (UKB data field 2247_1) 114,318 European ancestry cases, 323,449 European ancestry controls NA NR [11842647] (imputed) 4 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90042882 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hearing difficulty/problems: I am completely deaf (UKB data field 2247_99) 106 European ancestry cases, 437,661 European ancestry controls NA NR [11842647] (imputed) 1 deafness http://www.ebi.ac.uk/efo/EFO_0001063 GCST90042883 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Benign neoplasm of brain, cranial nerves, meninges (PheCode 225.1) 709 European ancestry cases, 455,639 European ancestry controls NA NR [11842647] (imputed) 0 nervous system benign neoplasm http://purl.obolibrary.org/obo/MONDO_0000648 GCST90042884 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hearing difficulty problems background noise (UKB data field 2257) 169,279 European ancestry cases, 277,792 European ancestry controls NA NR [11842647] (imputed) 1 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90042885 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: senior official in central government including members of the senior civil service and the equivalent in the diplomatic service, mps, meps (UKB data field 22601_11113200) 1,055 European ancestry cases, 111,223 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042886 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: director or chief executive of private organisation/company, company chairman or president, general manager (UKB data field 22601_11123211) 3,355 European ancestry cases, 108,923 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042887 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: senior official in local government including parish or town or county chief clerk, chief or superintendent rate collector, chief executive or director, councillor (UKB data field 22601_11133201) 1,517 European ancestry cases, 110,761 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042888 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: senior official of special interest organisation including general manager or director or executive or general secretary of charity, or trade union/association or religious organisation (UKB data field 22601_11143212) 2,588 European ancestry cases, 109,690 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042889 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: production, works or maintenance manager (UKB data field 22601_11212692) 736 European ancestry cases, 111,542 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042890 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: factory/works manager, shift manager (UKB data field 22601_11212693) 517 European ancestry cases, 111,761 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042891 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: manager in construction, clerk of works, site manager, contracts manager, highways manager (UKB data field 22601_11222591) 1,256 European ancestry cases, 111,022 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042892 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: manager in mining, energy production or water supply (UKB data field 22601_11232861) 339 European ancestry cases, 111,939 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042893 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: financial services manager, chartered secretary, banker, merchant or investment banker, finance director, tax manager (UKB data field 22601_11313221) 319 European ancestry cases, 111,959 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042894 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sales or marketing manager/director, export/import manager, business development manager, advertising/commercial manager (UKB data field 22601_11323222) 2,672 European ancestry cases, 109,606 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042895 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: purchasing manager/director (not retail), supplies manager (UKB data field 22601_11333223) 323 European ancestry cases, 111,955 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042896 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: customer care/relations manager, help desk manager (UKB data field 22601_11423230) 516 European ancestry cases, 111,762 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042905 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: personnel, human resources, training or industrial relations manager/director, recruitment manager/director (UKB data field 22601_11353225) 1,397 European ancestry cases, 110,881 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042899 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: ict or it manager, systems/data processing manager, telecom manager (UKB data field 22601_11363057) 1,984 European ancestry cases, 110,294 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042900 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: bank manager, bank section manager, building society manager, post/sub-post office manager (UKB data field 22601_11513250) 1,586 European ancestry cases, 110,692 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042907 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: office manager, account/payrolls manager, administration manager, litigation/solicitor's office manager (UKB data field 22601_11523251) 1,382 European ancestry cases, 110,896 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042908 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: road transport/traffic manager, haulage contractor/manager, taxi/courier service manager, bus/coach station manager, removals manager, shipping manager (UKB data field 22601_11612669) 392 European ancestry cases, 111,886 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042909 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: storage manager, stock control manager, container terminal manager (UKB data field 22601_11623349) 220 European ancestry cases, 112,058 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042910 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: retail or wholesale shop manager, showroom manager (UKB data field 22601_11633322) 2,104 European ancestry cases, 110,174 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042911 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: officer in armed forces (UKB data field 22601_11713433) 707 European ancestry cases, 111,571 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042912 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: police officer (inspector or above) (UKB data field 22601_11723441) 437 European ancestry cases, 111,841 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042913 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: senior officer in fire service including captain, commander, controller, firemaster, inspector, salvage officer, station officer, superintendent (UKB data field 22601_11733439) 169 European ancestry cases, 112,109 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042914 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: security service manager/owner, detective agency manager/owner (UKB data field 22601_11743454) 104 European ancestry cases, 112,174 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042915 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: manager of theatre, cinema, museum (UKB data field 22601_12253173) 240 European ancestry cases, 112,038 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042926 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: travel agency manager/owner, tourist manager (UKB data field 22601_12263368) 224 European ancestry cases, 112,054 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042927 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: property/housing/land manager (UKB data field 22601_12313231) 402 European ancestry cases, 111,876 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042928 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: garage manager/owner (UKB data field 22601_12322659) 126 European ancestry cases, 112,152 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042929 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: garage manager/proprietor (UKB data field 22601_12322938) 102 European ancestry cases, 112,176 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042930 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: hairdressing or beauty salon manager or proprietor/owner (UKB data field 22601_12333358) 330 European ancestry cases, 111,948 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042931 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: shopkeeper, shop owner, newsagent, wholesale/retail dealer (UKB data field 22601_12343321) 1,833 European ancestry cases, 110,445 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042932 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chemist (analytic, developmental, industrial, research) (UKB data field 22601_21113020) 1,292 European ancestry cases, 110,986 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042933 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: biologist, botanist, entomologist, zoologist, ecologist, microbiologist/pathologist/virologist/geneticist (not medically qualified) (UKB data field 22601_21123021) 797 European ancestry cases, 111,481 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042934 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: biochemist, medical laboratory scientific officer (UKB data field 22601_21123022) 549 European ancestry cases, 111,729 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042935 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: physicist, astronomer, geologist, geophysicist, meteorologist, oceanographer, seismologist (UKB data field 22601_21133023) 712 European ancestry cases, 111,566 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042936 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: mathematician (UKB data field 22601_21133024) 176 European ancestry cases, 112,102 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042937 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: civil engineer (UKB data field 22601_21212592) 572 European ancestry cases, 111,706 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042938 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: mining engineer in mining, water or natural gas/oil (UKB data field 22601_21212864) 128 European ancestry cases, 112,150 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042939 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: civil engineer, transport engineer, structural engineer, borough surveyor (UKB data field 22601_21213038) 415 European ancestry cases, 111,863 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042940 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: mechanical engineer (UKB data field 22601_21222679) 448 European ancestry cases, 111,830 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042941 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: mechanical engineer (UKB data field 22601_21222865) 130 European ancestry cases, 112,148 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042942 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: mechanical engineer, automobile engineer, aeronautical engineer, locomotive or marine engineer, welding engineer (UKB data field 22601_21223040) 1,402 European ancestry cases, 110,876 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042943 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrical engineer (UKB data field 22601_21232680) 111 European ancestry cases, 49,582 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042944 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrical engineer, generating engineer, power engineer, power transmission engineer (UKB data field 22601_21232866) 134 European ancestry cases, 112,144 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042945 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electrical engineer, generating engineer, power engineer, power transmission engineer (UKB data field 22601_21233041) 614 European ancestry cases, 111,664 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042946 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: electronics engineer, broadcasting engineer, microwave engineer, radar engineer, radio engineer (UKB data field 22601_21243042) 1,054 European ancestry cases, 111,224 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042947 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: chemical engineer, plastics engineer, pharmaceutical engineer (UKB data field 22601_21253043) 290 European ancestry cases, 111,988 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042948 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: design and development engineer, ergonomist (UKB data field 22601_21263044) 674 European ancestry cases, 111,604 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042949 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: production and process engineer (UKB data field 22601_21272684) 141 European ancestry cases, 112,137 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042950 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: hospital manager, health service manager, clinical manager, nursing service manager (UKB data field 22601_11813097) 1,188 European ancestry cases, 111,090 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042916 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: healthcare practice manager, dental practice manager, chiropody practice manager/owner (UKB data field 22601_11833099) 220 European ancestry cases, 112,058 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042917 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: social services manager, community care manager, welfare services manager (UKB data field 22601_11843115) 943 European ancestry cases, 111,335 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042918 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: residential manager, day care manager, nursing home manager, retirement home manager, convalescent home manager (UKB data field 22601_11853100) 422 European ancestry cases, 111,856 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042919 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: farm manager, agricultural manager (UKB data field 22601_12112477) 116 European ancestry cases, 112,162 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042920 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: hotel or guesthouse owner/manager; hostel warden, holiday camp manager, caravan/camping site owner/manager (UKB data field 22601_12213392) 514 European ancestry cases, 111,764 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042921 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: conference/events/exhibition manager (UKB data field 22601_12223226) 107 European ancestry cases, 112,171 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042922 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: restaurant or catering manager, restaurateur; canteen manager; takeaway food shop manager (UKB data field 22601_12233383) 737 European ancestry cases, 111,541 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042923 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: publican or manager of licensed premises, licensee, wine bar manager (UKB data field 22601_12243390) 492 European ancestry cases, 111,786 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042924 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: sports centre manager, riding school owner, sports ground manager, baths manager (UKB data field 22601_12253140) 143 European ancestry cases, 112,135 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042925 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: research or laboratory manager (UKB data field 22601_11373019) 1,381 European ancestry cases, 110,897 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042901 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: research and development manager (UKB data field 22601_11373228) 151 European ancestry cases, 112,127 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042902 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: quality assurance manager, quality control manager (UKB data field 22601_11412694) 353 European ancestry cases, 111,925 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042903 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: quality assurance manager, quality control manager (UKB data field 22601_11413229) 136 European ancestry cases, 112,142 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042904 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: public relations manager, media director, publicity manager (UKB data field 22601_11343163) 110 European ancestry cases, 112,168 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042897 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: advertising or public relations manager, media/publicity manager, campaign/fundraising manager (UKB data field 22601_11343224) 641 European ancestry cases, 111,637 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042898 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Job coding: customer care/relations manager, help desk manager (UKB data field 22601_11423324) 124 European ancestry cases, 112,154 European ancestry controls NA NR [11842647] (imputed) 0 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90042906 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pyogenic granuloma (PheCode 686.4) 361 European ancestry cases, 455,987 European ancestry controls NA NR [11842647] (imputed) 0 lobular capilliary hemangioma http://www.ebi.ac.uk/efo/EFO_0010830 GCST90044504 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other local infections of skin and subcutaneous tissue (PheCode 686) 745 European ancestry cases, 455,603 European ancestry controls NA NR [11842647] (imputed) 0 Erysipelothrix rhusiopathiae infectious disease http://www.ebi.ac.uk/efo/EFO_1000928 GCST90044505 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rash and other nonspecific skin eruption (PheCode 687.1) 628 European ancestry cases, 455,720 European ancestry controls NA NR [11842647] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90044506 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Localized superficial swelling, mass, or lump (PheCode 687.2) 219 European ancestry cases, 456,129 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044507 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disturbance of skin sensation (PheCode 687.4) 1,227 European ancestry cases, 455,121 European ancestry controls NA NR [11842647] (imputed) 0 disturbance of skin sensation http://www.ebi.ac.uk/efo/EFO_0009522 GCST90044508 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorder of skin and subcutaneous tissue, not otherwise specified (PheCode 689) 4,849 European ancestry cases, 451,499 European ancestry controls NA NR [11842647] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90044509 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other dyschromia (PheCode 694.2) 666 European ancestry cases, 455,682 European ancestry controls NA NR [11842647] (imputed) 0 pigmentation disease http://www.ebi.ac.uk/efo/EFO_1000755 GCST90044510 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Rosacea (PheCode 695.3) 144 European ancestry cases, 456,204 European ancestry controls NA NR [11842647] (imputed) 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90044511 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Systemic lupus erythematosus (PheCode 695.42) 122 European ancestry cases, 456,226 European ancestry controls NA NR [11842647] (imputed) 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90044512 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prurigo and Lichen (PheCode 695.7) 670 European ancestry cases, 455,678 European ancestry controls NA NR [11842647] (imputed) 0 lichen disease http://www.ebi.ac.uk/efo/EFO_1000724 GCST90044513 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Unspecified erythematous condition (PheCode 695.9) 129 European ancestry cases, 456,219 European ancestry controls NA NR [11842647] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90044514 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Psoriasis vulgaris (PheCode 696.41) 338 European ancestry cases, 456,010 European ancestry controls NA NR [11842647] (imputed) 0 psoriasis vulgaris http://www.ebi.ac.uk/efo/EFO_1001494 GCST90044515 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Psoriatic arthropathy (PheCode 696.42) 312 European ancestry cases, 456,036 European ancestry controls NA NR [11842647] (imputed) 0 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90044516 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Psoriasis (PheCode 696.4) 250 European ancestry cases, 456,098 European ancestry controls NA NR [11842647] (imputed) 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90044517 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sarcoidosis (PheCode 697) 257 European ancestry cases, 456,091 European ancestry controls NA NR [11842647] (imputed) 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90044518 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pruritus and related conditions (PheCode 698) 326 European ancestry cases, 456,022 European ancestry controls NA NR [11842647] (imputed) 0 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST90044519 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Corns and callosities (PheCode 700) 111 European ancestry cases, 456,237 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044520 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Scar conditions and fibrosis of skin (PheCode 701.2) 1,887 European ancestry cases, 454,461 European ancestry controls NA NR [11842647] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90044521 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Keloid scar (PheCode 701.4) 201 European ancestry cases, 456,147 European ancestry controls NA NR [11842647] (imputed) 0 Keloid http://www.ebi.ac.uk/efo/EFO_0004212 GCST90044522 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Abnormal granulation tissue (PheCode 701.5) 364 European ancestry cases, 455,984 European ancestry controls NA NR [11842647] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90044523 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other hypertrophic and atrophic conditions of skin (PheCode 701) 1,243 European ancestry cases, 455,105 European ancestry controls NA NR [11842647] (imputed) 0 Follicular Cyst http://www.ebi.ac.uk/efo/EFO_1001329 GCST90044524 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Actinic keratosis (PheCode 702.1) 2,033 European ancestry cases, 454,315 European ancestry controls NA NR [11842647] (imputed) 0 actinic keratosis http://www.ebi.ac.uk/efo/EFO_0002496 GCST90044525 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Seborrheic keratosis (PheCode 702.2) 2,684 European ancestry cases, 453,664 European ancestry controls NA NR [11842647] (imputed) 0 seborrheic keratosis http://www.ebi.ac.uk/efo/EFO_0005584 GCST90044526 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ingrowing nail (PheCode 703.1) 868 European ancestry cases, 455,480 European ancestry controls NA NR [11842647] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90044527 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diseases of nail, not otherwise specified (PheCode 703) 310 European ancestry cases, 456,038 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044528 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Preeclampsia and eclampsia (PheCode 642.1) 256 European ancestry cases, 247,284 European ancestry controls NA NR [11842647] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90044479 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hyperemesis gravidarum (PheCode 643.1) 146 European ancestry cases, 247,394 European ancestry controls NA NR [11842647] (imputed) 0 hyperemesis gravidarum http://www.ebi.ac.uk/efo/EFO_1000971 GCST90044480 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Late pregnancy and failed induction (PheCode 645) 643 European ancestry cases, 246,897 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044481 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other complications of pregnancy NEC (PheCode 646) 2,265 European ancestry cases, 245,275 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044482 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Infections of genitourinary tract during pregnancy (PheCode 647.1) 157 European ancestry cases, 247,383 European ancestry controls NA NR [11842647] (imputed) 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90044483 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Diabetes or abnormal glucose tolerance complicating pregnancy (PheCode 649.1) 113 European ancestry cases, 247,427 European ancestry controls NA NR [11842647] (imputed) 0 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST90044484 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Multiple gestation (PheCode 651) 118 European ancestry cases, 247,422 European ancestry controls NA NR [11842647] (imputed) 0 multiple gestation http://www.ebi.ac.uk/efo/EFO_0009576 GCST90044485 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malposition and malpresentation of fetus or obstruction (PheCode 652) 1,302 European ancestry cases, 246,238 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044486 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Known or suspected fetal abnormality affecting management of mother (PheCode 655) 3,552 European ancestry cases, 243,988 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044487 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fetal distress and abnormal forces of labor (PheCode 661) 1,601 European ancestry cases, 245,939 European ancestry controls NA NR [11842647] (imputed) 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90044488 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complications of labor and delivery NEC (PheCode 669) 2,013 European ancestry cases, 245,527 European ancestry controls NA NR [11842647] (imputed) 0 placental retention http://www.ebi.ac.uk/efo/EFO_0009578 GCST90044489 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of accommodation lived in: A house or bungalow (UKB data field 670_1) 412,014 European ancestry cases, 42,866 European ancestry controls NA NR [11842647] (imputed) 0 environmental factor http://www.ebi.ac.uk/efo/EFO_0000469 GCST90044490 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of accommodation lived in: A flat, maisonette or apartment (UKB data field 670_2) 41,105 European ancestry cases, 413,775 European ancestry controls NA NR [11842647] (imputed) 0 environmental factor http://www.ebi.ac.uk/efo/EFO_0000469 GCST90044491 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of accommodation lived in: Mobile or temporary structure (i.e. caravan) (UKB data field 670_3) 616 European ancestry cases, 454,264 European ancestry controls NA NR [11842647] (imputed) 0 environmental factor http://www.ebi.ac.uk/efo/EFO_0000469 GCST90044492 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type of accommodation lived in: Sheltered accommodation (UKB data field 670_4) 1,097 European ancestry cases, 453,783 European ancestry controls NA NR [11842647] (imputed) 0 environmental factor http://www.ebi.ac.uk/efo/EFO_0000469 GCST90044493 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other complications of the puerperium NEC (PheCode 674) 159 European ancestry cases, 247,381 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044494 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cellulitis and abscess of fingers/toes (PheCode 681.1) 425 European ancestry cases, 455,923 European ancestry controls NA NR [11842647] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90044495 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cellulitis and abscess of face/neck (PheCode 681.2) 414 European ancestry cases, 455,934 European ancestry controls NA NR [11842647] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90044496 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cellulitis and abscess of arm/hand (PheCode 681.3) 4,576 European ancestry cases, 451,772 European ancestry controls NA NR [11842647] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90044497 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cellulitis and abscess of leg, except foot (PheCode 681.5) 4,576 European ancestry cases, 451,772 European ancestry controls NA NR [11842647] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90044498 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cellulitis and abscess of foot, toe (PheCode 681.6) 4,576 European ancestry cases, 451,772 European ancestry controls NA NR [11842647] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90044499 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cellulitis and abscess of trunk (PheCode 681.7) 230 European ancestry cases, 456,118 European ancestry controls NA NR [11842647] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90044500 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Superficial cellulitis and abscess (PheCode 681) 337 European ancestry cases, 456,011 European ancestry controls NA NR [11842647] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90044501 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Carbuncle and furuncle (PheCode 686.1) 2,298 European ancestry cases, 454,050 European ancestry controls NA NR [11842647] (imputed) 0 Furuncle, carbuncle http://purl.obolibrary.org/obo/HP_0020083, http://www.ebi.ac.uk/efo/EFO_1000674 GCST90044502 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pilonidal cyst (PheCode 686.3) 512 European ancestry cases, 455,836 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044503 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mucous polyp of cervix (PheCode 622.2) 2,503 European ancestry cases, 245,037 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044454 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Polyp of female genital organs (PheCode 622) 165 European ancestry cases, 247,375 European ancestry controls NA NR [11842647] (imputed) 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90044455 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hypertrophy of female genital organs (PheCode 623) 351 European ancestry cases, 247,189 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044456 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dystrophy of female genital tract (PheCode 624.1) 164 European ancestry cases, 247,376 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044457 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. stress incontinence, female (PheCode 624.9) 5,093 European ancestry cases, 451,255 European ancestry controls NA NR [11842647] (imputed) 0 stress-related disorder http://www.ebi.ac.uk/efo/EFO_0010098 GCST90044458 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dyspareunia (PheCode 625.1) 537 European ancestry cases, 247,003 European ancestry controls NA NR [11842647] (imputed) 0 Dyspareunia http://purl.obolibrary.org/obo/HP_0030016 GCST90044459 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain and other symptoms associated with female genital organs (PheCode 625) 1,107 European ancestry cases, 246,433 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044460 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Excessive or frequent menstruation (PheCode 626.12) 7,013 European ancestry cases, 240,527 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044461 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Irregular menstrual cycle (PheCode 626.13) 1,326 European ancestry cases, 246,214 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044462 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Irregular menstrual bleeding (PheCode 626.14) 2,838 European ancestry cases, 244,702 European ancestry controls NA NR [11842647] (imputed) 0 Menstrual disorder http://www.ebi.ac.uk/efo/EFO_0010270 GCST90044463 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Irregular menstrual cycle/bleeding (PheCode 626.1) 1,530 European ancestry cases, 246,010 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044464 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dysmenorrhea (PheCode 626.2) 413 European ancestry cases, 247,127 European ancestry controls NA NR [11842647] (imputed) 0 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90044465 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Infertility, female (PheCode 626.8) 899 European ancestry cases, 246,641 European ancestry controls NA NR [11842647] (imputed) 0 female infertility http://www.ebi.ac.uk/efo/EFO_0008560 GCST90044466 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of menstruation and other abnormal bleeding from female genital tract (PheCode 626) 1,242 European ancestry cases, 246,298 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044467 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Postmenopausal bleeding (PheCode 627.1) 7,694 European ancestry cases, 239,846 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044468 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptomatic menopause (PheCode 627.2) 125 European ancestry cases, 247,415 European ancestry controls NA NR [11842647] (imputed) 0 menopause http://www.ebi.ac.uk/efo/EFO_0003922 GCST90044469 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Postmenopausal atrophic vaginitis (PheCode 627.3) 285 European ancestry cases, 247,255 European ancestry controls NA NR [11842647] (imputed) 0 menopause, Atrophic Vaginitis http://www.ebi.ac.uk/efo/EFO_0003922, http://www.ebi.ac.uk/efo/EFO_1001271 GCST90044470 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Premenopausal menorrhagia (PheCode 627.4) 235 European ancestry cases, 247,305 European ancestry controls NA NR [11842647] (imputed) 0 Menorrhagia, menopause http://purl.obolibrary.org/obo/HP_0000132, http://www.ebi.ac.uk/efo/EFO_0003922 GCST90044471 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Menopausal and postmenopausal disorders (PheCode 627) 357 European ancestry cases, 247,183 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044472 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ovarian cyst (PheCode 628) 2,608 European ancestry cases, 244,932 European ancestry controls NA NR [11842647] (imputed) 0 Ovarian cyst http://purl.obolibrary.org/obo/HP_0000138 GCST90044473 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Missed abortion/Hydatidiform mole (PheCode 634.1) 1,311 European ancestry cases, 246,229 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044474 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Ectopic pregnancy (PheCode 634.3) 317 European ancestry cases, 247,223 European ancestry controls NA NR [11842647] (imputed) 0 Ectopic pregnancy http://purl.obolibrary.org/obo/HP_0031456 GCST90044475 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Miscarriage; stillbirth (PheCode 634) 4,058 European ancestry cases, 243,482 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044476 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Antepartum hemorrhage, abruptio placentae, and placenta previa (PheCode 635.2) 782 European ancestry cases, 246,758 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044477 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hemorrhage in early pregnancy (PheCode 636.3) 993 European ancestry cases, 246,547 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044478 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure or diabetes: Cholesterol lowering medication (UKB data field 6177_1) 47,652 European ancestry cases, 159,003 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044429 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure or diabetes: PHESANT recoding (UKB data field 6177_100) 137,862 European ancestry cases, 68,793 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044430 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure or diabetes: Blood pressure medication (UKB data field 6177_2) 51,268 European ancestry cases, 155,387 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044431 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Medication for cholesterol, blood pressure or diabetes: Insulin (UKB data field 6177_3) 2,851 European ancestry cases, 203,804 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044432 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral and other dietary supplements: Fish oil (including cod liver oil) (UKB data field 6179_1) 144,080 European ancestry cases, 310,745 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044433 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral and other dietary supplements: PHESANT recoding (UKB data field 6179_100) 258,456 European ancestry cases, 196,369 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044434 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral and other dietary supplements: Glucosamine (UKB data field 6179_2) 88,339 European ancestry cases, 366,486 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044435 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral and other dietary supplements: Calcium (UKB data field 6179_3) 30,724 European ancestry cases, 424,101 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044436 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral and other dietary supplements: Zinc (UKB data field 6179_4) 18,478 European ancestry cases, 436,347 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044437 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral and other dietary supplements: Iron (UKB data field 6179_5) 13,865 European ancestry cases, 440,960 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044438 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mineral and other dietary supplements: Selenium (UKB data field 6179_6) 10,834 European ancestry cases, 443,991 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90044439 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders secondary to childbirth, surgery, trauma (PheCode 617) 181 European ancestry cases, 247,359 European ancestry controls NA NR [11842647] (imputed) 0 female genital tract fistula http://www.ebi.ac.uk/efo/EFO_0009524 GCST90044440 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prolapse of vaginal walls (PheCode 618.1) 5,543 European ancestry cases, 450,805 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044441 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Uterine/Uterovaginal prolapse (PheCode 618.2) 4,580 European ancestry cases, 242,960 European ancestry controls NA NR [11842647] (imputed) 0 uterine prolapse http://www.ebi.ac.uk/efo/EFO_1001864 GCST90044442 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Prolapse of vaginal vault after hysterectomy (PheCode 618.5) 451 European ancestry cases, 247,089 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044443 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vaginal enterocele, congenital or acquired (PheCode 618.6) 284 European ancestry cases, 247,256 European ancestry controls NA NR [11842647] (imputed) 0 Hernia of the abdominal wall http://purl.obolibrary.org/obo/HP_0004299 GCST90044444 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Genital prolapse (PheCode 618) 126 European ancestry cases, 247,414 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044445 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Noninflammatory disorders of ovary, fallopian tube, and broad ligament (PheCode 619.1) 286 European ancestry cases, 247,254 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044446 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Disorders of uterus, NEC (PheCode 619.2) 946 European ancestry cases, 246,594 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044447 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Noninflammatory disorders of cervix (PheCode 619.3) 981 European ancestry cases, 246,559 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90044448 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Noninflammatory disorders of vagina (PheCode 619.4) 1,027 European ancestry cases, 246,513 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044449 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Noninflammatory disorders of vulva and perineum (PheCode 619.5) 1,144 European ancestry cases, 246,396 European ancestry controls NA NR [11842647] (imputed) 0 Bartholin gland disease http://www.ebi.ac.uk/efo/EFO_0009469 GCST90044450 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Noninflammatory female genital disorders (PheCode 619) 142 European ancestry cases, 247,398 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044451 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Endometrial hyperplasia (PheCode 621) 742 European ancestry cases, 246,798 European ancestry controls NA NR [11842647] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90044452 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Polyp of corpus uteri (PheCode 622.1) 6,552 European ancestry cases, 240,988 European ancestry controls NA NR [11842647] (imputed) 0 uterine polyp http://www.ebi.ac.uk/efo/EFO_0009484 GCST90044453 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Facial pain (UKB data field 6159_2) 8,483 European ancestry cases, 446,789 European ancestry controls NA NR [11842647] (imputed) 0 facial pain http://www.ebi.ac.uk/efo/EFO_0009625 GCST90044404 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Neck or shoulder pain (UKB data field 6159_3) 104,845 European ancestry cases, 350,427 European ancestry controls NA NR [11842647] (imputed) 0 Shoulder pain, Neck pain http://purl.obolibrary.org/obo/HP_0030834, http://purl.obolibrary.org/obo/HP_0030833 GCST90044405 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Back pain (UKB data field 6159_4) 116,509 European ancestry cases, 338,763 European ancestry controls NA NR [11842647] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90044406 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Stomach or abdominal pain (UKB data field 6159_5) 38,915 European ancestry cases, 416,357 European ancestry controls NA NR [11842647] (imputed) 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90044407 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Hip pain (UKB data field 6159_6) 51,504 European ancestry cases, 403,768 European ancestry controls NA NR [11842647] (imputed) 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90044408 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Knee pain (UKB data field 6159_7) 97,408 European ancestry cases, 357,864 European ancestry controls NA NR [11842647] (imputed) 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90044409 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Pain all over the body (UKB data field 6159_8) 7,209 European ancestry cases, 448,063 European ancestry controls NA NR [11842647] (imputed) 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90044410 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Endometriosis (PheCode 615) 1,937 European ancestry cases, 245,603 European ancestry controls NA NR [11842647] (imputed) 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90044411 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leisure/social activities: Sports club or gym (UKB data field 6160_1) 136,413 European ancestry cases, 318,400 European ancestry controls NA NR [11842647] (imputed) 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90044412 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leisure/social activities: PHESANT recoding (UKB data field 6160_100) 137,762 European ancestry cases, 317,051 European ancestry controls NA NR [11842647] (imputed) 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90044413 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leisure/social activities: Pub or social club (UKB data field 6160_2) 124,626 European ancestry cases, 330,187 European ancestry controls NA NR [11842647] (imputed) 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90044414 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leisure/social activities: Religious group (UKB data field 6160_3) 66,860 European ancestry cases, 387,953 European ancestry controls NA NR [11842647] (imputed) 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90044415 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leisure/social activities: Adult education class (UKB data field 6160_4) 32,682 European ancestry cases, 422,131 European ancestry controls NA NR [11842647] (imputed) 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90044416 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Leisure/social activities: Other group activity (UKB data field 6160_5) 100,552 European ancestry cases, 354,261 European ancestry controls NA NR [11842647] (imputed) 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90044417 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of transport used (excluding work): Car/motor vehicle (UKB data field 6162_1) 358,970 European ancestry cases, 94,958 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044418 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of transport used (excluding work): PHESANT recoding (UKB data field 6162_100) 1,018 European ancestry cases, 452,910 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044419 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of transport used (excluding work): Walk (UKB data field 6162_2) 222,804 European ancestry cases, 231,124 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044420 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of transport used (excluding work): Public transport (UKB data field 6162_3) 136,590 European ancestry cases, 317,338 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044421 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of transport used (excluding work): Cycle (UKB data field 6162_4) 32,679 European ancestry cases, 421,249 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044422 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of physical activity in last 4 weeks: Walking for pleasure (not as a means of transport) (UKB data field 6164_1) 325,316 European ancestry cases, 128,522 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044423 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of physical activity in last 4 weeks: PHESANT recoding (UKB data field 6164_100) 27,372 European ancestry cases, 426,466 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044424 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of physical activity in last 4 weeks: Other exercises (eg: swimming, cycling, keep fit, bowling) (UKB data field 6164_2) 219,338 European ancestry cases, 234,500 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044425 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of physical activity in last 4 weeks: Strenuous sports (UKB data field 6164_3) 46,784 European ancestry cases, 407,054 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044426 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of physical activity in last 4 weeks: Light DIY (eg: pruning, watering the lawn) (UKB data field 6164_4) 233,765 European ancestry cases, 220,073 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044427 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Types of physical activity in last 4 weeks: Heavy DIY (eg: weeding, lawn mowing, carpentry, digging) (UKB data field 6164_5) 195,399 European ancestry cases, 258,439 European ancestry controls NA NR [11842647] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90044428 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: PHESANT recoding (UKB data field 6155_100) 311,362 European ancestry cases, 142,429 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044379 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: Vitamin B (UKB data field 6155_2) 19,006 European ancestry cases, 434,785 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044380 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: Vitamin C (UKB data field 6155_3) 39,182 European ancestry cases, 414,609 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044381 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: Vitamin D (UKB data field 6155_4) 17,531 European ancestry cases, 436,260 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044382 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: Vitamin E (UKB data field 6155_5) 13,264 European ancestry cases, 440,527 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044383 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: Folic acid or Folate (Vit B9) (UKB data field 6155_6) 9,819 European ancestry cases, 443,972 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044384 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin and mineral supplements: Multivitamins +/- minerals (UKB data field 6155_7) 98,123 European ancestry cases, 355,668 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90044385 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manic/hyper symptoms: PHESANT recoding (UKB data field 6156_100) 11,007 European ancestry cases, 19,657 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044386 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manic/hyper symptoms: I was more active than usual (UKB data field 6156_11) 7,709 European ancestry cases, 22,955 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044387 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manic/hyper symptoms: I was more talkative than usual (UKB data field 6156_12) 6,379 European ancestry cases, 24,285 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044388 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manic/hyper symptoms: I needed less sleep than usual (UKB data field 6156_13) 4,158 European ancestry cases, 26,506 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044389 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manic/hyper symptoms: I was more creative or had more ideas than usual (UKB data field 6156_14) 3,663 European ancestry cases, 27,001 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044390 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Manic/hyper symptoms: All of the above (UKB data field 6156_15) 3,106 European ancestry cases, 27,558 European ancestry controls NA NR [11842647] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90044391 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why stopped smoking: Illness or ill health (UKB data field 6157_1) 13,585 European ancestry cases, 98,915 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044392 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why stopped smoking: PHESANT recoding (UKB data field 6157_100) 22,607 European ancestry cases, 89,893 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044393 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why stopped smoking: Doctor's advice (UKB data field 6157_2) 8,102 European ancestry cases, 104,398 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044394 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why stopped smoking: Health precaution (UKB data field 6157_3) 70,520 European ancestry cases, 41,980 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044395 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why stopped smoking: Financial reasons (UKB data field 6157_4) 27,532 European ancestry cases, 84,968 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044396 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why reduced smoking: Illness or ill health (UKB data field 6158_1) 2,065 European ancestry cases, 12,669 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044397 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why reduced smoking: PHESANT recoding (UKB data field 6158_100) 4,245 European ancestry cases, 10,489 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044398 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why reduced smoking: Doctor's advice (UKB data field 6158_2) 2,092 European ancestry cases, 12,642 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044399 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why reduced smoking: Health precaution (UKB data field 6158_3) 6,968 European ancestry cases, 7,766 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044400 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Why reduced smoking: Financial reasons (UKB data field 6158_4) 3,971 European ancestry cases, 10,763 European ancestry controls NA NR [11842647] (imputed) 0 smoking behavior http://www.ebi.ac.uk/efo/EFO_0004318 GCST90044401 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: Headache (UKB data field 6159_1) 91,724 European ancestry cases, 363,548 European ancestry controls NA NR [11842647] (imputed) 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90044402 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pain type(s) experienced in last month: PHESANT recoding (UKB data field 6159_100) 182,205 European ancestry cases, 273,067 European ancestry controls NA NR [11842647] (imputed) 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90044403 Genome-wide genotyping array 2022-06-01 35308900 Joo J 2022-02-21 AMIA Annu Symp Proc www.ncbi.nlm.nih.gov/pubmed/35308900 Gene-Based Analysis Reveals Sex-Specific Genetic Risk Factors of COPD. Chronic obstructive pulmonary disease 12,958 British ancestry male cases, 95,631 British ancestry male controls NA NR [NR] (imputed) 19 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90103984 Genome-wide genotyping array 2022-06-01 35308900 Joo J 2022-02-21 AMIA Annu Symp Proc www.ncbi.nlm.nih.gov/pubmed/35308900 Gene-Based Analysis Reveals Sex-Specific Genetic Risk Factors of COPD. Chronic obstructive pulmonary disease 11,311 British ancestry female cases, 123,714 British ancestry female controls NA NR [NR] (imputed) 15 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90103985 Genome-wide genotyping array 2022-04-29 34613391 Ko H 2021-10-06 Brain www.ncbi.nlm.nih.gov/pubmed/34613391 Genome-wide association study of occupational attainment as a proxy for cognitive reserve. Occupational attainment 248,847 European ancestry individuals NA Affymetrix [9575249] (imputed) 30 occupational attainment http://www.ebi.ac.uk/efo/EFO_0020977 GCST90102253 Genome-wide genotyping array 2022-09-09 35974158 Bibi S 2022-08-16 Pediatr Res www.ncbi.nlm.nih.gov/pubmed/35974158 Polygenic risk scores and the need for pharmacotherapy in neonatal abstinence syndrome. Neonatal abstinence syndrome 59 African American cases, 35 African American controls, 231 European ancestry cases, 151 European ancestry controls NA Illumina [NR] (imputed) 20 neonatal abstinence syndrome http://www.ebi.ac.uk/efo/EFO_0005799 GCST90134522 Genome-wide genotyping array 2022-09-09 35974158 Bibi S 2022-08-16 Pediatr Res www.ncbi.nlm.nih.gov/pubmed/35974158 Polygenic risk scores and the need for pharmacotherapy in neonatal abstinence syndrome. Neonatal abstinence syndrome 231 European ancestry cases, 151 European ancestry controls NA Illumina [NR] (imputed) 20 neonatal abstinence syndrome http://www.ebi.ac.uk/efo/EFO_0005799 GCST90134523 Genome-wide genotyping array 2022-09-09 35974158 Bibi S 2022-08-16 Pediatr Res www.ncbi.nlm.nih.gov/pubmed/35974158 Polygenic risk scores and the need for pharmacotherapy in neonatal abstinence syndrome. Neonatal abstinence syndrome 59 African American cases, 35 African American controls NA Illumina [NR] (imputed) 18 neonatal abstinence syndrome http://www.ebi.ac.uk/efo/EFO_0005799 GCST90134524 Genome-wide genotyping array 2022-04-20 34801968 Wu Q 2021-11-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34801968 Multi-stage metabolomics and genetic analyses identified metabolite biomarkers of metabolic syndrome and their genetic determinants. Docosapentaenoic acid levels 1,062 East Asian ancestry individuals 227 East Asian ancestry individuals Illumina [40001312] (imputed) 0 docosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0006809 GCST90096805 Genome-wide genotyping array 2022-04-20 34801968 Wu Q 2021-11-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34801968 Multi-stage metabolomics and genetic analyses identified metabolite biomarkers of metabolic syndrome and their genetic determinants. L-Phenylalanine levels 1,062 East Asian ancestry individuals 227 East Asian ancestry individuals Illumina [40001312] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90096806 Genome-wide genotyping array 2022-04-20 34801968 Wu Q 2021-11-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34801968 Multi-stage metabolomics and genetic analyses identified metabolite biomarkers of metabolic syndrome and their genetic determinants. Propionylcarnitine levels 1,062 East Asian ancestry individuals 227 East Asian ancestry individuals Illumina [40001312] (imputed) 0 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90096807 Genome-wide genotyping array 2022-04-20 34801968 Wu Q 2021-11-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34801968 Multi-stage metabolomics and genetic analyses identified metabolite biomarkers of metabolic syndrome and their genetic determinants. Lysophosphatidylcholine(15:0) levels 1,062 East Asian ancestry individuals 227 East Asian ancestry individuals Illumina [40001312] (imputed) 3 lysophosphatidylcholine 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0020941 GCST90096808 Genome-wide genotyping array 2022-04-20 34801968 Wu Q 2021-11-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34801968 Multi-stage metabolomics and genetic analyses identified metabolite biomarkers of metabolic syndrome and their genetic determinants. Lysophosphatidylcholine(14:0) levels 1,062 East Asian ancestry individuals 227 East Asian ancestry individuals Illumina [40001312] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90096809 Genome-wide genotyping array 2022-01-06 30547231 Ahluwalia TS 2018-12-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/30547231 A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria. Albuminuria 13,226 European ancestry individuals 23,364 European ancestry individuals Illumina [142397] 1 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST012618 Exome genotyping array [Exome array] 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 1 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129321 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 2 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 3 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129322 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 3 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129323 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 4 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129324 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 5 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129325 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 6 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129326 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 7 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 3 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129327 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 8 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129328 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 9 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129329 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 10 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 4 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129330 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 11 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129331 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 12 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129332 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 13 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129333 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 14 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129334 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 15 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129335 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 16 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 4 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129336 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 17 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129337 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 18 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129338 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 19 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129339 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 20 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129340 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 21 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129341 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 22 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129342 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 23 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 3 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129343 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Immunoglobulin N-glycan 24 levels 2,020 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90129344 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 1 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129345 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 2 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129346 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 3 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129347 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 4 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129348 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 5 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129349 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 6 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129350 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 7 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129351 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 8 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129352 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 9 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129353 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 10 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129354 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 11 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129355 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 12 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129356 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 13 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129357 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 14 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129358 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 15 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129359 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 16 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129360 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 17 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129361 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 18 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 0 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129362 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 19 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129363 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 20 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 3 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129364 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 21 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 3 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129365 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 22 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129366 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 23 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 4 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129367 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 24 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129368 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 25 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 3 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129369 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 26 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129370 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 27 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 4 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129371 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 28 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129372 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 29 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129373 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 30 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129374 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 31 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129375 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 32 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 1 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129376 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 33 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129377 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 34 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129378 Genome-wide genotyping array 2022-07-18 35332118 Landini A 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332118 Genetic regulation of post-translational modification of two distinct proteins. Transferrin N-glycan 35 levels 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals NA NR [10700000] (imputed) 2 transferrin glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0021537 GCST90129379 Genome-wide genotyping array 2022-06-08 35203716 Kuznetsova MV 2022-02-21 Biomedicines www.ncbi.nlm.nih.gov/pubmed/35203716 Familial Predisposition to Leiomyomata: Searching for Protective Genetic Factors. Family history of uterine fibroids 20 cases, 14 controls NA NR [906600] 0 family history of uterine fibroids http://www.ebi.ac.uk/efo/EFO_0021423 GCST90103980 Genome-wide genotyping array 2022-07-25 35654975 Vujkovic M 2022-06-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35654975 A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Chronic elevation of alanine aminotransferase (cALT) levels 95,472 European ancestry cases, 68,725 European ancestry controls, 23,977 African American cases, 13,387 African American controls, 7,650 Hispanic cases, 7,468 Hispanic controls, 1,088 Asian ancestry cases, 828 Asian ancestry controls NA NR [NR] (imputed) 77 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90129601 Genome-wide genotyping array 2022-07-25 35654975 Vujkovic M 2022-06-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35654975 A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Chronic elevation of alanine aminotransferase (cALT) levels 95,472 European ancestry cases, 68,725 European ancestry controls NA NR [NR] (imputed) 55 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90129602 Genome-wide genotyping array 2022-07-25 35654975 Vujkovic M 2022-06-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35654975 A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Chronic elevation of alanine aminotransferase (cALT) levels 23,977 African American cases, 13,387 African American controls NA NR [NR] (imputed) 8 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90129603 Genome-wide genotyping array 2022-07-25 35654975 Vujkovic M 2022-06-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35654975 A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Chronic elevation of alanine aminotransferase (cALT) levels 7,650 Hispanic cases, 7,468 Hispanic controls NA NR [NR] (imputed) 3 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90129604 Genome-wide genotyping array 2022-07-25 35654975 Vujkovic M 2022-06-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35654975 A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. Chronic elevation of alanine aminotransferase (cALT) levels 1,088 Asian ancestry cases, 828 Asian ancestry controls NA NR [NR] (imputed) 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90129605 Genome-wide genotyping array 2021-12-15 34791234 Tyrmi JS 2021-11-13 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/34791234 Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome. Polycystic ovary syndrome (adjusted for age) 797 European ancestry cases, 140,558 European ancestry controls 2,812 European ancestry cases, 229,788 European ancestry controls NR [24154061] (imputed) 7 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST90044902 Genome-wide genotyping array 2021-12-15 34791234 Tyrmi JS 2021-11-13 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/34791234 Leveraging Northern European population history: novel low-frequency variants for polycystic ovary syndrome. Polycystic ovary syndrome (adjusted for age and BMI) 482 European ancestry cases, 91,631 European ancestry controls 2,137 European ancestry cases, 68,690 European ancestry controls NR [24481103] (imputed) 5 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST90044903 Genome-wide genotyping array 2022-03-18 34834357 Velasco-Ruiz A 2021-11-16 Pharmaceutics www.ncbi.nlm.nih.gov/pubmed/34834357 POLRMT as a Novel Susceptibility Gene for Cardiotoxicity in Epirubicin Treatment of Breast Cancer Patients. Anthracycline-induced cardiotoxicity in breast cancer 137 European ancestry cases, 90 European ancestry controls 59 European ancestry cases, 64 European ancestry controls Illumina [725785] (imputed) 0 cardiotoxicity, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_1001482, http://www.ebi.ac.uk/efo/EFO_0005257 GCST90095481 Genome-wide genotyping array 2022-03-18 34834357 Velasco-Ruiz A 2021-11-16 Pharmaceutics www.ncbi.nlm.nih.gov/pubmed/34834357 POLRMT as a Novel Susceptibility Gene for Cardiotoxicity in Epirubicin Treatment of Breast Cancer Patients. Anthracycline-induced cardiotoxicity in breast cancer 45 European ancestry cases, 90 European ancestry controls 77 European ancestry individuals Illumina [725785] (imputed) 1 cardiotoxicity, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_1001482, http://www.ebi.ac.uk/efo/EFO_0005257 GCST90095482 Genome-wide genotyping array 2022-06-22 35267517 Barnekow E 2022-02-25 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/35267517 A Swedish Genome-Wide Haplotype Association Analysis Identifies a Novel Breast Cancer Susceptibility Locus in 8p21.2 and Characterizes Three Loci on Chromosomes 10, 11 and 16. Breast cancer 3,200 Swedish ancestry cases, 5,021 Swedish ancestry controls NA Illumina [332906] (imputed) 3 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90104709 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium- and chloride-dependent neutral and basic amino acid transporter B(0+) levels (SLC6A14.13053.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sodium- and chloride-dependent neutral and basic amino acid transporter B(0+) measurement http://www.ebi.ac.uk/efo/EFO_0803304 GCST90242849 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium-coupled monocarboxylate transporter 1 levels (SLC5A8.13691.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sodium-coupled monocarboxylate transporter 1 measurement http://www.ebi.ac.uk/efo/EFO_0802076 GCST90242850 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium-independent sulfate anion transporter levels (SLC26A11.13502.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sodium-independent sulfate anion transporter measurement http://www.ebi.ac.uk/efo/EFO_0803087 GCST90242851 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium/iodide cotransporter levels (SLC5A5.12826.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sodium/iodide cotransporter measurement http://www.ebi.ac.uk/efo/EFO_0803088 GCST90242852 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium/potassium-transporting ATPase subunit alpha-1 levels (ATP1A1.11993.227.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 sodium/potassium-transporting ATPase subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0802077 GCST90242853 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium/potassium-transporting ATPase subunit beta-2 levels (ATP1B2.7218.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sodium/potassium-transporting ATPase subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0802078 GCST90242854 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Soluble calcium-activated nucleotidase 1 levels (CANT1.6480.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 soluble calcium-activated nucleotidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803089 GCST90242855 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Solute carrier family 22 member 16 levels (SLC22A16.9969.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 solute carrier family 22 member 16 measurement http://www.ebi.ac.uk/efo/EFO_0802079 GCST90242856 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Solute carrier family 35 member G2 levels (SLC35G2.13501.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 solute carrier family 35 member G2 measurement http://www.ebi.ac.uk/efo/EFO_0802080 GCST90242857 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Solute carrier family 41 member 2 levels (SLC41A2.12511.83.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 solute carrier family 41 member 2 measurement http://www.ebi.ac.uk/efo/EFO_0803090 GCST90242858 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Solute carrier organic anion transporter family member 5A1 levels (SLCO5A1.11669.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 solute carrier organic anion transporter family member 5A1 measurement http://www.ebi.ac.uk/efo/EFO_0803091 GCST90242859 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Somatostatin-28 levels (SST.5957.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 somatostatin-28 measurement http://www.ebi.ac.uk/efo/EFO_0020745 GCST90242860 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Somatotropin levels (GH1.8462.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 somatotropin measurement http://www.ebi.ac.uk/efo/EFO_0022017 GCST90242861 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sortilin levels (SORT1.11300.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sortilin measurement http://www.ebi.ac.uk/efo/EFO_0600000 GCST90242862 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sorting nexin-1 levels (SNX1.8807.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sorting nexin-1 measurement http://www.ebi.ac.uk/efo/EFO_0803092 GCST90242863 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sorting nexin-17 levels (SNX17.12845.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sorting nexin-17 measurement http://www.ebi.ac.uk/efo/EFO_0803093 GCST90242864 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sorting nexin-4 levels (SNX4.3903.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sorting nexin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020747 GCST90242865 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sorting nexin-7 levels (SNX7.14245.195.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sorting nexin-7 measurement http://www.ebi.ac.uk/efo/EFO_0803094 GCST90242866 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sorting nexin-8 levels (SNX8.6925.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sorting nexin-8 measurement http://www.ebi.ac.uk/efo/EFO_0803095 GCST90242867 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SPARC levels (SPARC.3043.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90242868 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SPARC levels (SPARC.14110.200.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90242869 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SPARC-like protein 1 levels (SPARCL1.4467.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90242870 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SPARC-like protein 1 levels (SPARCL1.13707.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90242871 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SPARC-related modular calcium-binding protein 1 levels (SMOC1.13118.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 sPARC-related modular calcium-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021868 GCST90242872 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Spastin levels (SPAST.8388.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 spastin measurement http://www.ebi.ac.uk/efo/EFO_0803096 GCST90242873 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Golgi SNAP receptor complex member 1 levels (GOSR1.7805.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Golgi SNAP receptor complex member 1 measurement http://www.ebi.ac.uk/efo/EFO_0801651 GCST90241313 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GRAM domain-containing protein 1C levels (GRAMD1C.8842.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 GRAM domain-containing protein 1C measurement http://www.ebi.ac.uk/efo/EFO_0801652 GCST90241314 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GRAM domain-containing protein 1C levels (GRAMD1C.8336.267.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GRAM domain-containing protein 1C measurement http://www.ebi.ac.uk/efo/EFO_0801652 GCST90241315 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Grancalcin levels (GCA.12594.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 grancalcin measurement http://www.ebi.ac.uk/efo/EFO_0801653 GCST90241316 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granulins levels (GRN.4992.49.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90241317 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granulocyte colony-stimulating factor levels (CSF3.8952.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90241318 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granulocyte colony-stimulating factor receptor levels (CSF3R.2719.3.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 granulocyte colony-stimulating factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020416 GCST90241319 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granulocyte-macrophage colony-stimulating factor levels (CSF2.4697.59.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 granulocyte-macrophage colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0020417 GCST90241320 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granulocyte-macrophage colony-stimulating factor receptor subunit alpha levels (CSF2RA.10438.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 granulocyte-macrophage colony-stimulating factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0802579 GCST90241321 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granulysin levels (GNLY.3195.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90241322 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GTP cyclohydrolase 1 levels (GCH1.11185.145.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GTP cyclohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802583 GCST90241358 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granzyme A levels (GZMA.3440.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90241323 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granzyme B levels (GZMB.4133.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 granzyme b measurement http://www.ebi.ac.uk/efo/EFO_0020418 GCST90241324 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granzyme B levels (GZMB.14041.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 granzyme b measurement http://www.ebi.ac.uk/efo/EFO_0020418 GCST90241325 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granzyme H levels (GZMH.3373.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 granzyme h measurement http://www.ebi.ac.uk/efo/EFO_0020419 GCST90241326 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granzyme K levels (GZMK.9545.156.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 granzyme K measurement http://www.ebi.ac.uk/efo/EFO_0801654 GCST90241327 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Granzyme M levels (GZMM.5704.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 granzyme M measurement http://www.ebi.ac.uk/efo/EFO_0801655 GCST90241328 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GRB2-related adapter protein levels (GRAP.12820.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GRB2-related adapter protein measurement http://www.ebi.ac.uk/efo/EFO_0802580 GCST90241329 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GRB2-related adapter protein 2 levels (GRAP2.5265.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90241330 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gremlin-1 levels (GREM1.4449.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gremlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020421 GCST90241331 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gremlin-2 levels (GREM2.5598.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gremlin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801656 GCST90241332 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gro-beta/gamma levels (CXCL3.CXCL2.3148.49.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gro-beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0020422 GCST90241333 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gro-beta/gamma levels (CXCL3.CXCL2.2986.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gro-beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0020422 GCST90241334 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Group 10 secretory phospholipase A2 levels (PLA2G10.2949.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 group 10 secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020423 GCST90241335 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Group IIE secretory phospholipase A2 levels (PLA2G2E.13670.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 group IIe secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020424 GCST90241336 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Group IIE secretory phospholipase A2 levels (PLA2G2E.2447.7.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 group IIe secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020424 GCST90241337 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth factor receptor-bound protein 7 levels (GRB7.11281.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 growth factor receptor-bound protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0801659 GCST90241343 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 11 levels (GDF11.14582.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90241347 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GTP-binding protein Di-Ras3 levels (DIRAS3.12406.119.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GTP-binding protein Di-Ras3 measurement http://www.ebi.ac.uk/efo/EFO_0802584 GCST90241359 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GTP-binding protein GEM levels (GEM.12817.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 GTP-binding protein GEM measurement http://www.ebi.ac.uk/efo/EFO_0801660 GCST90241360 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GTPase KRas levels (KRAS.5193.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GTPase kras measurement http://www.ebi.ac.uk/efo/EFO_0020432 GCST90241361 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanine deaminase levels (GDA.12667.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 guanine deaminase measurement http://www.ebi.ac.uk/efo/EFO_0802585 GCST90241362 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 6 levels (FAS.5392.73.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90243179 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 6 levels (FAS.9218.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90243180 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 6B levels (TNFRSF6B.5070.76.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tumor necrosis factor receptor superfamily member 6B measurement http://www.ebi.ac.uk/efo/EFO_0020815 GCST90243181 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 8 levels (TNFRSF8.2605.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0020816 GCST90243182 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member EDAR levels (EDAR.2977.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 tumor necrosis factor receptor superfamily member EDAR measurement http://www.ebi.ac.uk/efo/EFO_0008310 GCST90243183 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor-inducible gene 6 protein levels (TNFAIP6.5036.50.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tumor necrosis factor-inducible gene 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0008311 GCST90243184 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor protein 63 levels (TP63.10040.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor protein 63 measurement http://www.ebi.ac.uk/efo/EFO_0803202 GCST90243185 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor protein p53-inducible protein 11 levels (TP53I11.13022.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tumor protein p53-inducible protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0802169 GCST90243186 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor susceptibility gene 101 protein levels (TSG101.13044.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor susceptibility gene 101 protein measurement http://www.ebi.ac.uk/efo/EFO_0803203 GCST90243187 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor-associated calcium signal transducer 2 levels (TACSTD2.2619.72.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor-associated calcium signal transducer 2 measurement http://www.ebi.ac.uk/efo/EFO_0020817 GCST90243188 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor-associated calcium signal transducer 2 levels (TACSTD2.14034.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor-associated calcium signal transducer 2 measurement http://www.ebi.ac.uk/efo/EFO_0020817 GCST90243189 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Twinfilin-1 levels (TWF1.12871.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 twinfilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0803204 GCST90243190 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Twisted gastrulation protein homolog 1 levels (TWSG1.9234.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 twisted gastrulation protein homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0803205 GCST90243191 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. TYMS opposite strand protein levels (TYMSOS.8263.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 TYMS opposite strand protein measurement http://www.ebi.ac.uk/efo/EFO_0803206 GCST90243192 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Type 2 lactosamine alpha-2,3-sialyltransferase levels (ST3GAL6.6947.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 type 2 lactosamine alpha-2,3-sialyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802170 GCST90243193 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Type III endosome membrane protein TEMP levels (C1orf210.8088.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 type III endosome membrane protein TEMP measurement http://www.ebi.ac.uk/efo/EFO_0803207 GCST90243194 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase ABL1 levels (ABL1.3341.33.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase ABL1 measurement http://www.ebi.ac.uk/efo/EFO_0020818 GCST90243195 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase BTK levels (BTK.3416.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase BTK measurement http://www.ebi.ac.uk/efo/EFO_0020819 GCST90243196 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase CSK levels (CSK.3363.31.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase CSK measurement http://www.ebi.ac.uk/efo/EFO_0020820 GCST90243197 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase Fgr levels (FGR.3810.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase FGR measurement http://www.ebi.ac.uk/efo/EFO_0020822 GCST90243198 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase FRK levels (FRK.10034.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase FRK measurement http://www.ebi.ac.uk/efo/EFO_0802171 GCST90243199 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase Fyn levels (FYN.4550.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase FYN measurement http://www.ebi.ac.uk/efo/EFO_0020823 GCST90243200 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase HCK levels (HCK.3374.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase HCK measurement http://www.ebi.ac.uk/efo/EFO_0020824 GCST90243201 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase JAK2 levels (JAK2.4998.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 tyrosine-protein kinase JAK2 measurement http://www.ebi.ac.uk/efo/EFO_0020825 GCST90243202 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase Lck levels (LCK.4560.34.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90243203 Genome-wide genotyping array 2022-04-01 34570997 Wang F 2021-09-24 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34570997 A genome-wide scan on individual typology angle found variants at SLC24A2 associated with skin color variation in Chinese populations. Skin pigmentation 6,964 Chinese ancestry individuals 1,787 Chinese ancestry individuals, 266 Hispanic or Latin American individuals Illumina [8039700] (imputed) 3 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90100219 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase Lck levels (LCK.3452.17.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90243204 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase Lyn levels (LYN.3453.87.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase lyn measurement http://www.ebi.ac.uk/efo/EFO_0020827 GCST90243205 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase Lyn, isoform B levels (LYN.3381.24.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase LYN, isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020828 GCST90243206 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase receptor Tie-1, soluble levels (TIE1.2844.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 tyrosine-protein kinase receptor Tie-1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008312 GCST90243207 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase receptor TYRO3 levels (TYRO3.2611.72.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase receptor TYRO3 measurement http://www.ebi.ac.uk/efo/EFO_0020829 GCST90243208 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase RYK levels (RYK.5583.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase RYK measurement http://www.ebi.ac.uk/efo/EFO_0803208 GCST90243209 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase transmembrane receptor ROR1 levels (ROR1.2590.69.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase transmembrane receptor ROR1 measurement http://www.ebi.ac.uk/efo/EFO_0020831 GCST90243210 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase transmembrane receptor ROR2 levels (ROR2.7861.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase transmembrane receptor ROR2 measurement http://www.ebi.ac.uk/efo/EFO_0803209 GCST90243211 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase Yes levels (YES1.2878.66.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase YES measurement http://www.ebi.ac.uk/efo/EFO_0020832 GCST90243212 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase ZAP-70 levels (ZAP70.4476.22.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein kinase ZAP-70 measurement http://www.ebi.ac.uk/efo/EFO_0020833 GCST90243213 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase ZAP-70 levels (ZAP70.3837.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase ZAP-70 measurement http://www.ebi.ac.uk/efo/EFO_0020833 GCST90243214 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein kinase ZAP-70 levels (ZAP70.4475.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein kinase ZAP-70 measurement http://www.ebi.ac.uk/efo/EFO_0020833 GCST90243215 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein phosphatase non-receptor type 1 levels (PTPN1.3005.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90243216 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein phosphatase non-receptor type 11 levels (PTPN11.3397.7.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90243217 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein phosphatase non-receptor type 2 levels (PTPN2.3401.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosine-protein phosphatase non-receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0020836 GCST90243218 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein phosphatase non-receptor type 4 levels (PTPN4.14254.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 tyrosine-protein phosphatase non-receptor type 4 measurement http://www.ebi.ac.uk/efo/EFO_0802172 GCST90243219 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein phosphatase non-receptor type 7 levels (PTPN7.14688.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein phosphatase non-receptor type 7 measurement http://www.ebi.ac.uk/efo/EFO_0802173 GCST90243220 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein phosphatase non-receptor type 9 levels (PTPN9.12633.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tyrosine-protein phosphatase non-receptor type 9 measurement http://www.ebi.ac.uk/efo/EFO_0802174 GCST90243221 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosine-protein phosphatase non-receptor type substrate 1 levels (SIRPA.5430.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tyrosine-protein phosphatase non-receptor type substrate 1 measurement http://www.ebi.ac.uk/efo/EFO_0802175 GCST90243222 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tyrosyl-DNA phosphodiesterase 1 levels (TDP1.10073.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tyrosyl-DNA phosphodiesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803210 GCST90243223 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. U1 small nuclear ribonucleoprotein A levels (SNRPA.12678.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 U1 small nuclear ribonucleoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0802176 GCST90243224 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. U6 snRNA phosphodiesterase levels (USB1.11328.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 U6 snRNA phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0803211 GCST90243225 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquilin-4 levels (UBQLN4.12720.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquilin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802177 GCST90243226 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquinol-cytochrome-c reductase complex assembly factor 3 levels (UQCC3.8228.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquinol-cytochrome-c reductase complex assembly factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0803212 GCST90243227 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin levels (RPS27A.4474.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin measurement http://www.ebi.ac.uk/efo/EFO_0020839 GCST90243228 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratin, type I cytoskeletal 17 levels (KRT17.12923.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 keratin, type I cytoskeletal 17 measurement http://www.ebi.ac.uk/efo/EFO_0802672 GCST90241689 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratin, type I cytoskeletal 18 levels (KRT18.5354.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 keratin, type I cytoskeletal 18 measurement http://www.ebi.ac.uk/efo/EFO_0020517 GCST90241690 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratin, type I cytoskeletal 20 levels (KRT20.12975.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 keratin, type I cytoskeletal 20 measurement http://www.ebi.ac.uk/efo/EFO_0802673 GCST90241691 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratin, type II cytoskeletal 5 levels (KRT5.11177.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 keratin, type II cytoskeletal 5 measurement http://www.ebi.ac.uk/efo/EFO_0802674 GCST90241692 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratin, type II cytoskeletal 7 levels (KRT7.11383.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 keratin, type II cytoskeletal 7 measurement http://www.ebi.ac.uk/efo/EFO_0802675 GCST90241693 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratinocyte differentiation-associated protein levels (KRTDAP.5739.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 keratinocyte differentiation-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801743 GCST90241694 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratinocyte-associated transmembrane protein 2 levels (KCT2.6365.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 keratinocyte-associated transmembrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802676 GCST90241695 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 2DL2 levels (KIR2DL2.7773.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 killer cell immunoglobulin-like receptor 2DL2 measurement http://www.ebi.ac.uk/efo/EFO_0801744 GCST90241696 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 2DL4 levels (KIR2DL4.5095.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90241697 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 2DL4 levels (KIR2DL4.9245.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90241698 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 2DL5A levels (KIR2DL5A.8000.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 13 killer cell immunoglobulin-like receptor 2DL5A measurement http://www.ebi.ac.uk/efo/EFO_0801745 GCST90241699 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 2DL5A levels (KIR2DL5A.7799.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 killer cell immunoglobulin-like receptor 2DL5A measurement http://www.ebi.ac.uk/efo/EFO_0801745 GCST90241700 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 2DS2 levels (KIR2DS2.10428.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 killer cell immunoglobulin-like receptor 2DS2 measurement http://www.ebi.ac.uk/efo/EFO_0801746 GCST90241701 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 3DL2 levels (KIR3DL2.5096.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 killer cell immunoglobulin-like receptor 3DL2 measurement http://www.ebi.ac.uk/efo/EFO_0020518 GCST90241702 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 3DL3 levels (KIR3DL3.7944.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 killer cell immunoglobulin-like receptor 3DL3 measurement http://www.ebi.ac.uk/efo/EFO_0802677 GCST90241703 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell immunoglobulin-like receptor 3DS1 levels (KIR3DS1.5097.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 killer cell immunoglobulin-like receptor 3DS1 measurement http://www.ebi.ac.uk/efo/EFO_0020519 GCST90241704 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell lectin-like receptor subfamily F member 1 levels (KLRF1.5098.79.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 killer cell lectin-like receptor subfamily F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020520 GCST90241705 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Killer cell lectin-like receptor subfamily F member 1 levels (KLRF1.7756.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 killer cell lectin-like receptor subfamily F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020520 GCST90241706 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kin of IRRE-like protein 2 levels (KIRREL2.7958.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kin of IRRE-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802678 GCST90241707 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kin of IRRE-like protein 2 levels (KIRREL2.9917.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kin of IRRE-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802678 GCST90241708 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kin of IRRE-like protein 3 levels (KIRREL3.4557.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kin of IRRE-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020521 GCST90241709 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kinesin-like protein KIF16B levels (KIF16B.11672.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kinesin-like protein KIF16B measurement http://www.ebi.ac.uk/efo/EFO_0801747 GCST90241710 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kinesin-like protein KIF1C levels (KIF1C.9899.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kinesin-like protein KIF1C measurement http://www.ebi.ac.uk/efo/EFO_0802679 GCST90241711 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kinesin-like protein KIF23 levels (KIF23.5228.25.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kinesin-like protein KIF23 measurement http://www.ebi.ac.uk/efo/EFO_0020522 GCST90241712 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kinetochore protein NDC80 homolog levels (NDC80.12730.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kinetochore protein NDC80 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801748 GCST90241713 Genome-wide genotyping array 2022-03-23 34737440 Lona-Durazo F 2021-11-04 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34737440 A large Canadian cohort provides insights into the genetic architecture of human hair colour. Blond vs. brown/black hair color 12,398 European ancestry individuals NA Affymetrix, Illumina [32876187] (imputed) 18 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST90095476 Genome-wide genotyping array 2022-03-23 34737440 Lona-Durazo F 2021-11-04 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34737440 A large Canadian cohort provides insights into the genetic architecture of human hair colour. Brown vs. black hair color 10,990 European ancestry individuals NA Affymetrix, Illumina [32876187] (imputed) 7 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST90095477 Genome-wide genotyping array 2022-03-23 34737440 Lona-Durazo F 2021-11-04 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34737440 A large Canadian cohort provides insights into the genetic architecture of human hair colour. Red vs. brown/black hair color 10,450 European ancestry individuals NA Affymetrix, Illumina [32876187] (imputed) 14 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST90095478 Genome-wide genotyping array 2022-02-10 34706549 Olson NC 2021-10-28 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34706549 Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Blacks. Soluble urokinase plasminogen activator receptor levels 3,492 African American individuals NA NR [21944818] 3 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90093464 Genome-wide sequencing 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 26) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007206 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 27) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007207 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 28) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007208 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 29) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007209 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 30) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007210 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 31) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007211 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 32) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007212 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 33) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007213 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 34) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007214 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 35) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007215 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 36) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007216 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 37) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007217 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 38) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007218 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 39) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007219 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 40) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007220 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 41) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007221 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 42) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007222 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 43) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007223 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 44) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007224 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 45) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007225 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 46) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007226 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 47) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007227 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 48) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007228 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 49) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007229 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 50) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007230 Genome-wide genotyping array 2022-04-07 34976021 Li W 2021-12-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34976021 Identification of a Risk Locus at 7p22.3 for Schizophrenia and Bipolar Disorder in East Asian Populations. Schizophrenia or bipolar disorder 22,778 schizophrenia cases, 35,362 schizophrenia controls, 1,822 bipolar disorder cases, 4,650 bipolar disorder controls 4,918 Han Chinese ancestry schizophrenia cases, 5,506 Han Chinese ancestry controls NR [NR] (imputed) 2 bipolar disorder, schizophrenia http://purl.obolibrary.org/obo/MONDO_0004985, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90101737 Genome-wide genotyping array 2022-01-20 33679876 Irvin MR 2021-02-19 Front Genet www.ncbi.nlm.nih.gov/pubmed/33679876 Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population. Relative wall thickness 1,364 African ancestry individuals NA Illumina [397723] 1 heart relative wall thickness http://www.ebi.ac.uk/efo/EFO_0009286 GCST90093118 Exome-wide sequencing 2022-01-20 33679876 Irvin MR 2021-02-19 Front Genet www.ncbi.nlm.nih.gov/pubmed/33679876 Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population. Left ventricular internal dimension in diastole 1,364 African ancestry individuals NA Illumina [397723] 2 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST90093119 Exome-wide sequencing 2022-01-20 33679876 Irvin MR 2021-02-19 Front Genet www.ncbi.nlm.nih.gov/pubmed/33679876 Whole-Exome Sequencing and hiPSC Cardiomyocyte Models Identify MYRIP, TRAPPC11, and SLC27A6 of Potential Importance to Left Ventricular Hypertrophy in an African Ancestry Population. Left ventricular mass 1,364 African ancestry individuals NA Illumina [397723] 0 left ventricular mass http://www.ebi.ac.uk/efo/EFO_0009289 GCST90093120 Exome-wide sequencing 2022-01-14 33542107 Wan X 2021-02-04 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/33542107 Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium. Potassium levels 5,812 Old Order Amish (founder/genetic isolate) individuals NA Illumina [NR] 3 potassium measurement http://www.ebi.ac.uk/efo/EFO_0009283 GCST90093102 Exome-wide sequencing 2022-02-09 34269803 Casto A 2021-07-16 Blood www.ncbi.nlm.nih.gov/pubmed/34269803 Genetic Variants Associated with Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation. Cytomegalovirus reactivation after allogeneic hematopoietic cell transplantation (recipients) up to 1,301 European ancestry recipients up to 868 European ancestry recipients Affymetrix, Illumina [29826485] (imputed) 5 cytomegalovirus virus reactivation, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0020106, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90085702 Genome-wide genotyping array 2022-02-09 34269803 Casto A 2021-07-16 Blood www.ncbi.nlm.nih.gov/pubmed/34269803 Genetic Variants Associated with Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation. Cytomegalovirus high-level reactivation after allogeneic hematopoietic cell transplantation (recipients) up to 1,301 European ancestry recipients up to 868 European ancestry recipients Affymetrix, Illumina [29826485] (imputed) 3 cytomegalovirus virus reactivation, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0020106, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90085703 Genome-wide genotyping array 2022-02-09 34269803 Casto A 2021-07-16 Blood www.ncbi.nlm.nih.gov/pubmed/34269803 Genetic Variants Associated with Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation. Cytomegalovirus infection after allogeneic hematopoietic cell transplantation (recipients) up to 1,301 European ancestry recipients up to 868 European ancestry recipients Affymetrix, Illumina [29826485] (imputed) 4 cytomegalovirus infection, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0001062, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90085704 Genome-wide genotyping array 2022-02-09 34269803 Casto A 2021-07-16 Blood www.ncbi.nlm.nih.gov/pubmed/34269803 Genetic Variants Associated with Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation. Cytomegalovirus reactivation after allogeneic hematopoietic cell transplantation (donors) up to 1,301 European ancestry donors up to 868 European ancestry donors Affymetrix, Illumina [29826485] (imputed) 1 cytomegalovirus virus reactivation, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0020106, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90092527 Genome-wide genotyping array 2022-02-09 34269803 Casto A 2021-07-16 Blood www.ncbi.nlm.nih.gov/pubmed/34269803 Genetic Variants Associated with Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation. Cytomegalovirus high-level reactivation after allogeneic hematopoietic cell transplantation (donors) up to 1,301 European ancestry donors up to 868 European ancestry donors Affymetrix, Illumina [29826485] (imputed) 4 cytomegalovirus virus reactivation, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0020106, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90092528 Genome-wide genotyping array 2022-02-09 34269803 Casto A 2021-07-16 Blood www.ncbi.nlm.nih.gov/pubmed/34269803 Genetic Variants Associated with Cytomegalovirus Infection after Allogeneic Hematopoietic Cell Transplantation. Cytomegalovirus infection after allogeneic hematopoietic cell transplantation (donors) up to 1,301 European ancestry donors up to 868 European ancestry donors Affymetrix, Illumina [29826485] (imputed) 3 cytomegalovirus infection, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0001062, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90092529 Genome-wide genotyping array 2021-12-22 32226016 Hu Y 2020-03-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32226016 Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. High density lipoprotein cholesterol levels 17,641 African American individuals, 22,830 Hispanics ancestry individuals, 2,378 East Asian ancestry individuals, 1,912 Native Hawaiian ancestry individuals, 604 Native American ancestry individuals, 333 individuals, 22,887 European ancestry individuals up to 71,987 African American individuals, up to 34,899 Hispanics ancestry individuals, up to 315,133 European ancestry individuals, up to 9,593 Asian ancestry individuals, up to 94,674 European ancestry, East Asian ancestry, African American, South Asian ancestry, Hispanic individuals Affymetrix, Illumina [NR] (imputed) 19 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90090989 Genome-wide genotyping array 2021-12-22 32226016 Hu Y 2020-03-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32226016 Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Low density lipoprotein cholesterol levels 17,222 African American individuals, 22,406 Hispanics ancestry individuals, 2,316 East Asian ancestry individuals, 1,900 Native Hawaiian ancestry individuals, 591 Native American ancestry individuals, 321 individuals, 22,331 European ancestry individuals up to 71,987 African American individuals, up to 34,899 Hispanics ancestry individuals, up to 315,133 European ancestry individuals, up to 9,593 Asian ancestry individuals, up to 94,674 European ancestry, East Asian ancestry, African American, South Asian ancestry, Hispanic individuals Affymetrix, Illumina [NR] (imputed) 22 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90090990 Genome-wide genotyping array 2021-12-22 32226016 Hu Y 2020-03-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32226016 Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Total cholesterol levels 17,701 African American individuals, 22,954 Hispanics ancestry individuals, 2,387 East Asian ancestry individuals, 1,915 Native Hawaiian ancestry individuals, 604 Native American ancestry individuals, 340 individuals, 22,912 European ancestry individuals up to 71,987 African American individuals, up to 34,899 Hispanics ancestry individuals, up to 315,133 European ancestry individuals, up to 9,593 Asian ancestry individuals, up to 94,674 European ancestry, East Asian ancestry, African American, South Asian ancestry, Hispanic individuals Affymetrix, Illumina [NR] (imputed) 21 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90090991 Genome-wide genotyping array 2021-12-22 32226016 Hu Y 2020-03-30 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32226016 Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Total triglycerides levels 17,563 African American individuals, 23,077 Hispanics ancestry individuals, 2,381 East Asian ancestry individuals, 1,915 Native Hawaiian ancestry individuals, 604 Native American ancestry individuals, 360 individuals, 22,898 European ancestry individuals up to 71,987 African American individuals, up to 34,899 Hispanics ancestry individuals, up to 315,133 European ancestry individuals, up to 9,593 Asian ancestry individuals, up to 94,674 European ancestry, East Asian ancestry, African American, South Asian ancestry, Hispanic individuals Affymetrix, Illumina [NR] (imputed) 20 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90090992 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanine nucleotide exchange factor DBS levels (MCF2L.13934.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 guanine nucleotide exchange factor DBS measurement http://www.ebi.ac.uk/efo/EFO_0802586 GCST90241363 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanine nucleotide exchange factor VAV3 levels (VAV3.9830.109.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 guanine nucleotide exchange factor VAV3 measurement http://www.ebi.ac.uk/efo/EFO_0802587 GCST90241364 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-T2 levels (GNGT2.10917.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-T2 measurement http://www.ebi.ac.uk/efo/EFO_0802588 GCST90241365 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanine nucleotide-binding protein G(k) subunit alpha levels (GNAI3.12650.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 guanine nucleotide-binding protein G(k) subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801661 GCST90241366 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanylate cyclase activator 2B levels (GUCA2B.6223.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 guanylate cyclase activator 2B measurement http://www.ebi.ac.uk/efo/EFO_0802589 GCST90241367 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanylate-binding protein 6 levels (GBP6.7818.101.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 guanylate-binding protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801662 GCST90241368 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLAM family member 5 levels (CD84.3642.4.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90242830 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLAM family member 6 levels (SLAMF6.5128.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 SLAM family member 6 measurement http://www.ebi.ac.uk/efo/EFO_0020742 GCST90242831 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLAM family member 7 levels (SLAMF7.5487.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90242832 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLAM family member 7 levels (SLAMF7.7882.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90242833 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLAM family member 8 levels (SLAMF8.8994.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SLAM family member 8 measurement http://www.ebi.ac.uk/efo/EFO_0803079 GCST90242834 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLIT and NTRK-like protein 1 levels (SLITRK1.3643.90.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SLIT and NTRK-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021974 GCST90242835 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLIT and NTRK-like protein 3 levels (SLITRK3.10565.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 SLIT and NTRK-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802074 GCST90242836 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLIT and NTRK-like protein 4 levels (SLITRK4.7139.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SLIT and NTRK-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803080 GCST90242837 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLIT and NTRK-like protein 5 levels (SLITRK5.4568.17.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 slit and ntrk-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020743 GCST90242838 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Small conductance calcium-activated potassium channel protein 1 levels (KCNN1.13539.131.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 small conductance calcium-activated potassium channel protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803081 GCST90242839 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Small EDRK-rich factor 1 levels (SERF1A.7842.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 small EDRK-rich factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0803082 GCST90242840 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Small glutamine-rich tetratricopeptide repeat-containing protein alpha levels (SGTA.3868.8.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 small glutamine-rich tetratricopeptide repeat-containing protein alpha measurement http://www.ebi.ac.uk/efo/EFO_0020744 GCST90242841 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Small integral membrane protein 10 levels (SMIM10.9379.248.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 small integral membrane protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0803083 GCST90242842 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Small integral membrane protein 9 levels (SMIM9.8888.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 small integral membrane protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0802075 GCST90242843 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Small ubiquitin-related modifier 3 levels (SUMO3.14623.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 small ubiquitin-related modifier 3 measurement http://www.ebi.ac.uk/efo/EFO_0022025 GCST90242844 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Small ubiquitin-related modifier 3 levels (SUMO3.9169.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 small ubiquitin-related modifier 3 measurement http://www.ebi.ac.uk/efo/EFO_0022025 GCST90242845 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SNARE-associated protein Snapin levels (SNAPIN.6975.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SNARE-associated protein Snapin measurement http://www.ebi.ac.uk/efo/EFO_0803084 GCST90242846 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium channel subunit beta-2 levels (SCN2B.8353.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sodium channel subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0803085 GCST90242847 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sodium- and chloride-dependent glycine transporter 1 levels (SLC6A9.11653.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sodium- and chloride-dependent glycine transporter 1 measurement http://www.ebi.ac.uk/efo/EFO_0803086 GCST90242848 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; IFNβ-1a subcutaneous) 392 German and Swedish ancestry cases, 753 German and Swedish ancestry controls NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093327 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; IFNβ-1a intramuscular) 86 German and Swedish ancestry cases, 505 German and Swedish ancestry controls NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093328 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; IFNβ-1a subcutaneous and intramuscular) 478 German and Swedish ancestry cases, 1,258 German and Swedish ancestry controls NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093329 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; IFNβ-1b subcutaneous) 500 German and Swedish ancestry cases, 508 German and Swedish ancestry controls NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093330 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; all treatment preparations) 978 German and Swedish ancestry cases, 1,766 German and Swedish ancestry controls NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093331 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; IFNβ-1a subcutaneous) 1,145 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093332 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; IFNβ-1a intramuscular) 591 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093333 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; IFNβ-1a subcutaneous and intramuscular) 1,736 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093334 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; IFNβ-1b subcutaneous) 1,008 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093335 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; all treatment preparations) 2,744 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093336 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; IFNβ-1a subcutaneous) 1,146 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093337 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; IFNβ-1a intramuscular) 592 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093338 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; IFNβ-1a subcutaneous and intramuscular) 1,738 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093339 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; IFNβ-1b subcutaneous) 1,007 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093340 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; all treatment preparations) 2,745 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093341 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis in patients positive for neutralising antibodies (antibody titre; IFNβ-1a subcutaneous) 391 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093342 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis in patients positive for neutralising antibodies (antibody titre; IFNβ-1a intramuscular) 86 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093343 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis in patients positive for neutralising antibodies (antibody titre; IFNβ-1a subcutaneous and intramuscular) 477 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093344 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis in patients positive for neutralising antibodies (antibody titre; IFNβ-1b subcutaneous) 499 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093345 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis in patients positive for neutralising antibodies (antibody titre; all treatment preparations) 976 German and Swedish ancestry individuals NA Illumina [8197309] (imputed) 0 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093346 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; all treatment preparations) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093347 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; IFNβ-1b subcutaneous) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 2 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093348 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; IFNβ-1a subcutaneous and intramuscular) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 3 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093349 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-4 levels (IL4.2906.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802661 GCST90241639 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-4 receptor subunit alpha levels (IL4R.3055.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-4 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020507 GCST90241640 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-5 levels (IL5.3741.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-5 measurement http://www.ebi.ac.uk/efo/EFO_0801729 GCST90241641 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-5 levels (IL5.11071.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-5 measurement http://www.ebi.ac.uk/efo/EFO_0801729 GCST90241642 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-5 receptor subunit alpha levels (IL5RA.4491.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 interleukin-5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801730 GCST90241643 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-5 receptor subunit alpha levels (IL5RA.13686.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801730 GCST90241644 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-6 levels (IL6.2573.20.15) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90241645 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-6 levels (IL6.4673.13.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90241646 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-6 receptor subunit alpha levels (IL6R.4139.71.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 interleukin-6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801731 GCST90241647 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-6 receptor subunit alpha levels (IL6R.8092.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801731 GCST90241648 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-6 receptor subunit beta levels (IL6ST.2620.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 interleukin-6 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801732 GCST90241649 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-7 levels (IL7.14049.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-7 measurement http://www.ebi.ac.uk/efo/EFO_0802662 GCST90241650 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-7 receptor subunit alpha levels (IL7R.5089.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-7 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020508 GCST90241651 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-8 levels (CXCL8.3447.64.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST90241652 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-9 levels (IL9.8379.35.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-9 measurement http://www.ebi.ac.uk/efo/EFO_0802663 GCST90241653 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-9 levels (IL9.5834.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-9 measurement http://www.ebi.ac.uk/efo/EFO_0802663 GCST90241654 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intersectin-1 levels (ITSN1.14070.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 intersectin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801733 GCST90241655 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intestinal-type alkaline phosphatase levels (ALPI.10463.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 intestinal-type alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0801734 GCST90241656 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. IQ domain-containing protein F1 levels (IQCF1.7991.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 IQ domain-containing protein F1 measurement http://www.ebi.ac.uk/efo/EFO_0802664 GCST90241657 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Iron-sulfur cluster assembly enzyme ISCU, mitochondrial levels (ISCU.7201.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 iron-sulfur cluster assembly enzyme ISCU, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802665 GCST90241658 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Isochorismatase domain-containing protein 1 levels (ISOC1.9816.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 isochorismatase domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801735 GCST90241659 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Isoleucine--tRNA ligase, cytoplasmic levels (IARS.12815.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 isoleucine--tRNA ligase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0802666 GCST90241660 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. IST1 homolog levels (IST1.12434.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 IST1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801736 GCST90241661 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Isthmin-1 levels (ISM1.8355.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 isthmin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801737 GCST90241662 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Janus kinase and microtubule-interacting protein 3 levels (JAKMIP3.9068.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 janus kinase and microtubule-interacting protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801738 GCST90241663 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Junctional adhesion molecule B levels (JAM2.2997.8.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 junctional adhesion molecule B measurement http://www.ebi.ac.uk/efo/EFO_0020509 GCST90241664 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Junctional adhesion molecule C levels (JAM3.2998.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 junctional adhesion molecule C measurement http://www.ebi.ac.uk/efo/EFO_0020510 GCST90241665 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Junctional adhesion molecule-like levels (AMICA1.8232.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 junctional adhesion molecule-like measurement http://www.ebi.ac.uk/efo/EFO_0020511 GCST90241666 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Junctional adhesion molecule-like levels (AMICA1.5094.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 junctional adhesion molecule-like measurement http://www.ebi.ac.uk/efo/EFO_0020511 GCST90241667 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Junctophilin-1 levels (JPH1.6940.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 junctophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802667 GCST90241668 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Junctophilin-3 levels (JPH3.9089.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 junctophilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802668 GCST90241669 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-11 levels (KLK11.2831.29.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90241670 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-12 levels (KLK12.3199.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 kallikrein-12 measurement http://www.ebi.ac.uk/efo/EFO_0008194 GCST90241671 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-14 levels (KLK14.8620.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90241672 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-14 levels (KLK14.3681.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90241673 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-15 levels (KLK15.6491.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kallikrein-15 measurement http://www.ebi.ac.uk/efo/EFO_0802669 GCST90241674 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-4 levels (KLK4.2833.20.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kallikrein-4 measurement http://www.ebi.ac.uk/efo/EFO_0020514 GCST90241675 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-5 levels (KLK5.3201.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90241676 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-5 levels (KLK5.14039.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90241677 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-6 levels (KLK6.3450.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 kallikrein-6 measurement http://www.ebi.ac.uk/efo/EFO_0801739 GCST90241678 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-7 levels (KLK7.3378.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 kallikrein-7 measurement http://www.ebi.ac.uk/efo/EFO_0008195 GCST90241679 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-8 levels (KLK8.13708.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90241680 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallikrein-8 levels (KLK8.2834.54.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90241681 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallistatin levels (SERPINA4.3449.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90241682 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kallistatin levels (SERPINA4.14105.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90241683 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. KDEL motif-containing protein 2 levels (KDELC2.8296.117.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 KDEL motif-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801740 GCST90241684 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kelch-like protein 12 levels (KLHL12.12695.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kelch-like protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0802670 GCST90241685 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kelch-like protein 13 levels (KLHL13.12463.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kelch-like protein 13 measurement http://www.ebi.ac.uk/efo/EFO_0801741 GCST90241686 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kell blood group glycoprotein levels (KEL.7070.25.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kell blood group glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0802671 GCST90241687 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Keratin-associated protein 2-4 levels (KRTAP2.4.14615.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 keratin-associated protein 2-4 measurement http://www.ebi.ac.uk/efo/EFO_0801742 GCST90241688 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-20 levels (IL20.4138.25.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-20 measurement http://www.ebi.ac.uk/efo/EFO_0020496 GCST90241614 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-21 levels (IL21.7124.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 interleukin-21 measurement http://www.ebi.ac.uk/efo/EFO_0801724 GCST90241615 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-22 levels (IL22.2778.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90241616 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-22 receptor subunit alpha-1 levels (IL22RA1.3620.67.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90241617 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-22 receptor subunit alpha-1 levels (IL22RA1.9603.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90241618 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-22 receptor subunit alpha-2 levels (IL22RA2.5087.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90241619 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-22 receptor subunit alpha-2 levels (IL22RA2.9456.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90241620 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-23 levels (IL12B.IL23A.10365.132.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90241621 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-23 levels (IL12B.IL23A.4494.63.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90241622 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-23 receptor levels (IL23R.5088.175.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-23 receptor measurement http://www.ebi.ac.uk/efo/EFO_0801725 GCST90241623 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-24 levels (IL24.3321.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-24 measurement http://www.ebi.ac.uk/efo/EFO_0020502 GCST90241624 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-25 levels (IL25.4137.57.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-25 measurement http://www.ebi.ac.uk/efo/EFO_0801726 GCST90241625 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-27 levels (IL27.EBI3.2829.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-27 measurement http://www.ebi.ac.uk/efo/EFO_0010916 GCST90241626 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-27 receptor subunit alpha levels (IL27RA.5132.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-27 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801727 GCST90241627 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-3 levels (IL3.4717.55.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020503 GCST90241628 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-3 receptor subunit alpha levels (IL3RA.13744.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90241629 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-3 receptor subunit alpha levels (IL3RA.4490.65.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90241630 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-31 levels (IL31.10455.196.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-31 measurement http://www.ebi.ac.uk/efo/EFO_0801728 GCST90241631 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-31 receptor subunit alpha levels (IL31RA.8273.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-31 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0802658 GCST90241632 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-32 levels (IL32.9051.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-32 measurement http://www.ebi.ac.uk/efo/EFO_0802659 GCST90241633 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-34 levels (IL34.4556.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-34 measurement http://www.ebi.ac.uk/efo/EFO_0020505 GCST90241634 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-36 alpha levels (IL36A.10928.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-36 alpha measurement http://www.ebi.ac.uk/efo/EFO_0021851 GCST90241635 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-36 beta levels (IL36B.14149.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-36 beta measurement http://www.ebi.ac.uk/efo/EFO_0021955 GCST90241636 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-36 gamma levels (IL36G.9117.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-36 gamma measurement http://www.ebi.ac.uk/efo/EFO_0802660 GCST90241637 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-37 levels (IL37.2723.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-37 measurement http://www.ebi.ac.uk/efo/EFO_0020506 GCST90241638 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; IFNβ-1a subcutaneous) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093350 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Binding antibody response to interferon beta therapy in multiple sclerosis (antibody levels; all treatment preparations) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 5 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093351 Genome-wide genotyping array 2022-04-04 34862199 O'Connor MJ 2021-12-03 Diabetes www.ncbi.nlm.nih.gov/pubmed/34862199 Recessive Genome-wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes. Type 2 diabetes 33,139 European ancestry cases, 279,507 European ancestry controls 23,366 European ancestry cases, 78,547 European ancestry controls Affymetrix, Illumina [11634328] (imputed) 5 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90100587 Genome-wide genotyping array 2021-12-15 34777790 A Christensen M 2021-10-13 Ann Med Surg (Lond) www.ncbi.nlm.nih.gov/pubmed/34777790 An assessment of the effect of the genotype on postoperative venous thromboembolism risk in 140,831 surgical patients. Postoperative venous thromboembolism 799 cases, 140,032 controls NA Affymetrix [254068] 3 venous thromboembolism, response to surgery http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0009951 GCST90091240 Genome-wide genotyping array 2021-12-15 34777790 A Christensen M 2021-10-13 Ann Med Surg (Lond) www.ncbi.nlm.nih.gov/pubmed/34777790 An assessment of the effect of the genotype on postoperative venous thromboembolism risk in 140,831 surgical patients. Venous thromboembolism 6,260 cases, 355,414 controls NA Affymetrix [254068] 7 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90091241 Genome-wide genotyping array 2022-01-20 34748635 Miranda JP 2021-11-08 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/34748635 Genome-Wide Association Study And Polygenic Risk Scores Of Serum Dheas Levels In A Chilean Children Cohort. DHEAS levels 788 Hispanic or Latin American individuals NA Illumina [5510858] (imputed) 11 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90093090 Genome-wide genotyping array 2022-01-20 34748635 Miranda JP 2021-11-08 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/34748635 Genome-Wide Association Study And Polygenic Risk Scores Of Serum Dheas Levels In A Chilean Children Cohort. DHEAS levels 398 Hispanic or Latin American male individuals NA Illumina [5510858] (imputed) 9 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90093091 Genome-wide genotyping array 2022-01-20 34748635 Miranda JP 2021-11-08 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/34748635 Genome-Wide Association Study And Polygenic Risk Scores Of Serum Dheas Levels In A Chilean Children Cohort. DHEAS levels 390 Hispanic or Latin American female individuals NA Illumina [5510858] (imputed) 6 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90093092 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HLA class II histocompatibility antigen gamma chain levels (CD74.6974.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 HLA class II histocompatibility antigen gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0802607 GCST90241447 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HLA class II histocompatibility antigen, DM alpha chain levels (HLA.DMA.10639.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 HLA class II histocompatibility antigen, DM alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0801684 GCST90241448 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HLA class II histocompatibility antigen, DP beta 1 chain levels (HLA.DPB1.8755.202.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 HLA class II histocompatibility antigen, DP beta 1 chain measurement http://www.ebi.ac.uk/efo/EFO_0801685 GCST90241449 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HLA class II histocompatibility antigen, DQ alpha 2 chain levels (HLA.DQA2.7757.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 HLA class II histocompatibility antigen, DQ alpha 2 chain measurement http://www.ebi.ac.uk/efo/EFO_0801686 GCST90241450 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Homeobox protein TGIF2 levels (TGIF2.9847.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 homeobox protein TGIF2 measurement http://www.ebi.ac.uk/efo/EFO_0802608 GCST90241451 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Homeodomain-interacting protein kinase 3 levels (HIPK3.3443.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 homeodomain-interacting protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020457 GCST90241452 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Homogentisate 1,2-dioxygenase levels (HGD.9832.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 homogentisate 1,2-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0802609 GCST90241453 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HRAS-like suppressor 2 levels (HRASLS2.7822.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 HRAS-like suppressor 2 measurement http://www.ebi.ac.uk/efo/EFO_0802610 GCST90241454 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HRAS-like suppressor 3 levels (PLA2G16.7865.126.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 HRAS-like suppressor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802611 GCST90241455 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Human Chorionic Gonadotropin levels (CGA.CGB.4914.10.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90241456 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hyaluronan and proteoglycan link protein 1 levels (HAPLN1.3196.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hyaluronan and proteoglycan link protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020459 GCST90241457 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hyaluronidase-1 levels (HYAL1.8309.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hyaluronidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0802612 GCST90241458 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hydroxycarboxylic acid receptor 2 levels (HCAR2.13495.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hydroxycarboxylic acid receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0802613 GCST90241459 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hydroxymethylglutaryl-CoA synthase, cytoplasmic levels (HMGCS1.13496.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hydroxymethylglutaryl-CoA synthase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0802614 GCST90241460 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hydroxymethylglutaryl-CoA synthase, mitochondrial levels (HMGCS2.13704.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hydroxymethylglutaryl-CoA synthase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802615 GCST90241461 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hypoxia-inducible factor 1-alpha levels (HIF1A.13089.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hypoxia-inducible factor 1-alpha measurement http://www.ebi.ac.uk/efo/EFO_0021926 GCST90241462 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ICOS ligand levels (ICOSLG.9303.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90241463 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ICOS ligand levels (ICOSLG.5061.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90241464 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ig gamma-2, Kappa levels (NoneX.13230.174.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ig gamma-2, Kappa measurement http://www.ebi.ac.uk/efo/EFO_0802616 GCST90241465 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ig Kappa chain V-I region HK102- like levels (LOC652493.6561.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ig Kappa chain V-I region HK102- like measurement http://www.ebi.ac.uk/efo/EFO_0802617 GCST90241466 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. IGF-like family receptor 1 levels (IGFLR1.7244.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 IGF-like family receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801687 GCST90241467 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. IgLON family member 5 levels (IGLON5.6478.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 igLON family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0802618 GCST90241468 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immediate early response 3-interacting protein 1 levels (IER3IP1.6412.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immediate early response 3-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802619 GCST90241469 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin alpha Fc receptor levels (FCAR.4987.17.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin alpha fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0020462 GCST90241470 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin E levels (IGHE.IGK.IGL.4135.84.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin E measurement http://www.ebi.ac.uk/efo/EFO_0020464 GCST90241471 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stress-induced-phosphoprotein 1 levels (STIP1.5489.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 stress-induced-phosphoprotein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020755 GCST90242899 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stromal cell-derived factor 1 levels (CXCL12.3516.60.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 stromal cell-derived factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020756 GCST90242900 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stromal cell-derived factor 1 levels (CXCL12.2330.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 stromal cell-derived factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020756 GCST90242901 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stromal cell-derived factor 2-like protein 1 levels (SDF2L1.6990.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 stromal cell-derived factor 2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803105 GCST90242902 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stromal interaction molecule 1 levels (STIM1.9271.101.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 stromal interaction molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0802093 GCST90242903 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stromal membrane-associated protein 1 levels (SMAP1.11649.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 stromal membrane-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802094 GCST90242904 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stromelysin-2 levels (MMP10.8479.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 stromelysin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802095 GCST90242905 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stromelysin-2 levels (MMP10.3743.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 stromelysin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802095 GCST90242906 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Structural maintenance of chromosomes protein 3 levels (SMC3.14324.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 structural maintenance of chromosomes protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802096 GCST90242907 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Submaxillary gland androgen-regulated protein 3A levels (SMR3A.7838.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 submaxillary gland androgen-regulated protein 3A measurement http://www.ebi.ac.uk/efo/EFO_0802097 GCST90242908 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Submaxillary gland androgen-regulated protein 3B levels (SMR3B.8595.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 submaxillary gland androgen-regulated protein 3B measurement http://www.ebi.ac.uk/efo/EFO_0803106 GCST90242909 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Succinate dehydrogenase assembly factor 2, mitochondrial levels (SDHAF2.6420.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 succinate dehydrogenase assembly factor 2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0803107 GCST90242910 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sulfatase-modifying factor 1 levels (SUMF1.6941.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 sulfatase-modifying factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802098 GCST90242911 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sulfhydryl oxidase 1 levels (QSOX1.6217.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 sulfhydryl oxidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802099 GCST90242912 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sulfhydryl oxidase 1 levels (QSOX1.6070.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sulfhydryl oxidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802099 GCST90242913 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sulfhydryl oxidase 2 levels (QSOX2.8397.147.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 sulfhydryl oxidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802100 GCST90242914 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sulfiredoxin-1 levels (SRXN1.14268.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sulfiredoxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802101 GCST90242915 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sulfotransferase 4A1 levels (SULT4A1.8357.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sulfotransferase 4A1 measurement http://www.ebi.ac.uk/efo/EFO_0803108 GCST90242916 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SUMO-conjugating enzyme UBC9 levels (UBE2I.2877.3.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sumo-conjugating enzyme UBC9 measurement http://www.ebi.ac.uk/efo/EFO_0020757 GCST90242917 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SUN domain-containing protein 3 levels (SUN3.8852.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 SUN domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802102 GCST90242918 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SUN domain-containing protein 5 levels (SUN5.11260.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 SUN domain-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802103 GCST90242919 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Superoxide dismutase [Mn], mitochondrial levels (SOD2.5008.51.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 superoxide dismutase [Mn], mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008294 GCST90242920 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Suppressor of cytokine signaling 3 levels (SOCS3.11440.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 suppressor of cytokine signaling 3 measurement http://www.ebi.ac.uk/efo/EFO_0802104 GCST90242921 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Suppressor of cytokine signaling 7 levels (SOCS7.11657.86.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 suppressor of cytokine signaling 7 measurement http://www.ebi.ac.uk/efo/EFO_0803109 GCST90242922 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Suprabasin levels (SBSN.5724.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 suprabasin measurement http://www.ebi.ac.uk/efo/EFO_0803110 GCST90242923 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase P levels (GSTP1.13576.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90241288 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase theta-2B levels (GSTT2B.11273.176.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glutathione S-transferase theta-2B measurement http://www.ebi.ac.uk/efo/EFO_0802572 GCST90241289 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glyceraldehyde-3-phosphate dehydrogenase, testis-specific levels (GAPDHS.8004.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glyceraldehyde-3-phosphate dehydrogenase, testis-specific measurement http://www.ebi.ac.uk/efo/EFO_0802573 GCST90241290 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycerol-3-phosphate dehydrogenase 1-like protein levels (GPD1L.12420.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 glycerol-3-phosphate dehydrogenase 1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801640 GCST90241291 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycerophosphocholine phosphodiesterase GPCPD1 levels (GPCPD1.12786.61.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glycerophosphocholine phosphodiesterase GPCPD1 measurement http://www.ebi.ac.uk/efo/EFO_0802574 GCST90241292 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycine N-methyltransferase levels (GNMT.14006.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glycine N-methyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0801641 GCST90241293 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycogen phosphorylase, liver form levels (PYGL.11441.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glycogen phosphorylase, liver form measurement http://www.ebi.ac.uk/efo/EFO_0801642 GCST90241294 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycolipid transfer protein levels (GLTP.12513.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glycolipid transfer protein measurement http://www.ebi.ac.uk/efo/EFO_0802575 GCST90241295 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycolipid transfer protein domain-containing protein 2 levels (GLTPD2.7948.129.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glycolipid transfer protein domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801643 GCST90241296 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycophorin-A levels (GYPA.9389.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glycophorin-A measurement http://www.ebi.ac.uk/efo/EFO_0802576 GCST90241297 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycoprotein endo-alpha-1,2-mannosidase levels (MANEA.8014.359.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 glycoprotein endo-alpha-1,2-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801644 GCST90241298 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycoprotein hormone alpha-2 levels (GPHA2.6395.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glycoprotein hormone alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0801645 GCST90241299 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycoprotein hormones alpha chain levels (CGA.14056.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glycoprotein hormones alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0802577 GCST90241300 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycoprotein hormones alpha chain levels (CGA.TSHB.3521.16.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glycoprotein hormones alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0802577 GCST90241301 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycoprotein Xg levels (XG.8044.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glycoprotein Xg measurement http://www.ebi.ac.uk/efo/EFO_0801646 GCST90241302 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycosaminoglycan xylosylkinase levels (FAM20B.7198.197.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glycosaminoglycan xylosylkinase measurement http://www.ebi.ac.uk/efo/EFO_0801647 GCST90241303 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycosyltransferase 8 domain-containing protein 1 levels (GLT8D1.8955.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glycosyltransferase 8 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801648 GCST90241304 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycosyltransferase-like protein LARGE1 levels (LARGE.7935.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glycosyltransferase-like protein LARGE1 measurement http://www.ebi.ac.uk/efo/EFO_0802578 GCST90241305 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glycylpeptide N-tetradecanoyltransferase 1 levels (NMT1.5196.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glycylpeptide n-tetradecanoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020413 GCST90241306 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glypican-1 levels (GPC1.8697.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glypican-1 measurement http://www.ebi.ac.uk/efo/EFO_0801649 GCST90241307 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glypican-3 levels (GPC3.4842.62.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glypican-3 measurement http://www.ebi.ac.uk/efo/EFO_0020415 GCST90241308 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glypican-5 levels (GPC5.4991.12.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glypican-5 measurement http://www.ebi.ac.uk/efo/EFO_0008139 GCST90241309 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glypican-6 levels (GPC6.5350.14.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glypican-6 measurement http://www.ebi.ac.uk/efo/EFO_0021871 GCST90241310 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Golgi membrane protein 1 levels (GOLM1.8983.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 Golgi membrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801650 GCST90241311 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Golgi membrane protein 1 levels (GOLM1.8798.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Golgi membrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801650 GCST90241312 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Speckle-type POZ protein levels (SPOP.13727.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 speckle-type POZ protein measurement http://www.ebi.ac.uk/efo/EFO_0803097 GCST90242874 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Spectrin alpha chain, non-erythrocytic 1 levels (SPTAN1.5031.10.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 spectrin alpha chain, non-erythrocytic 1 measurement http://www.ebi.ac.uk/efo/EFO_0020749 GCST90242875 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sperm acrosome membrane-associated protein 3 levels (SPACA3.8076.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 sperm acrosome membrane-associated protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802081 GCST90242876 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sperm-associated antigen 11A levels (SPAG11A.5726.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sperm-associated antigen 11A measurement http://www.ebi.ac.uk/efo/EFO_0802082 GCST90242877 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sperm-associated antigen 11B levels (SPAG11B.5762.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sperm-associated antigen 11B measurement http://www.ebi.ac.uk/efo/EFO_0803098 GCST90242878 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Spermatogenesis-associated protein 20 levels (SPATA20.11117.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 spermatogenesis-associated protein 20 measurement http://www.ebi.ac.uk/efo/EFO_0802083 GCST90242879 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Spermatogenesis-associated protein 9 levels (SPATA9.7809.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 spermatogenesis-associated protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0803099 GCST90242880 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sphingosine kinase 2 levels (SPHK2.4468.21.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sphingosine kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020751 GCST90242881 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Spliceosome RNA helicase DDX39B levels (DDX39B.9742.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 spliceosome RNA helicase DDX39B measurement http://www.ebi.ac.uk/efo/EFO_0802084 GCST90242882 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Splicing factor 1 levels (SF1.12777.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 splicing factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802085 GCST90242883 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Splicing factor 3B subunit 4 levels (SF3B4.13449.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 splicing factor 3B subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0803100 GCST90242884 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Splicing factor U2AF 65 kDa subunit levels (U2AF2.13577.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 splicing factor U2AF 65 kDa subunit measurement http://www.ebi.ac.uk/efo/EFO_0803101 GCST90242885 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Spondin-1 levels (SPON1.4297.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90242886 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sprouty-related, EVH1 domain-containing protein 1 levels (SPRED1.8318.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sprouty-related, EVH1 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803102 GCST90242887 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SPRY domain-containing SOCS box protein 1 levels (SPSB1.13942.140.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SPRY domain-containing SOCS box protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803103 GCST90242888 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stabilin-1 levels (STAB1.14599.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 stabilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802086 GCST90242889 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stabilin-2 levels (STAB2.3399.31.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 stabilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020752 GCST90242890 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stanniocalcin-1 levels (STC1.4930.21.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 stanniocalcin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020753 GCST90242891 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stanniocalcin-2 levels (STC2.6231.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 stanniocalcin-2 measurement http://www.ebi.ac.uk/efo/EFO_0803104 GCST90242892 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stathmin-2 levels (STMN2.10900.272.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 stathmin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802087 GCST90242893 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stathmin-3 levels (STMN3.8019.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 stathmin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802088 GCST90242894 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stathmin-4 levels (STMN4.6267.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 stathmin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802089 GCST90242895 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Stem Cell Growth Factor-beta levels (CLEC11A.2966.65.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 stem Cell Growth Factor-beta measurement http://www.ebi.ac.uk/efo/EFO_0802090 GCST90242896 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Steroidogenic acute regulatory protein, mitochondrial levels (STAR.10085.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 steroidogenic acute regulatory protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802091 GCST90242897 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating levels (NSDHL.8038.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating measurement http://www.ebi.ac.uk/efo/EFO_0802092 GCST90242898 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heat shock 70 kDa protein 1-like levels (HSPA1L.12041.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 heat shock 70 kDa protein 1-like measurement http://www.ebi.ac.uk/efo/EFO_0801665 GCST90241372 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heat shock 70 kDa protein 6 levels (HSPA6.13672.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 heat shock 70 kDa protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801666 GCST90241373 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heat shock protein HSP 90-alpha/beta levels (HSP90AA1.HSP90AB1.2626.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heat shock protein hsp 90-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020435 GCST90241374 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heat shock protein HSP 90-beta levels (HSP90AB1.5467.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heat shock protein HSP 90-beta measurement http://www.ebi.ac.uk/efo/EFO_0021991 GCST90241375 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hematopoietic progenitor cell antigen CD34 levels (CD34.9023.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 hematopoietic progenitor cell antigen CD34 measurement http://www.ebi.ac.uk/efo/EFO_0801667 GCST90241376 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hematopoietic progenitor cell antigen CD34 levels (CD34.11285.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hematopoietic progenitor cell antigen CD34 measurement http://www.ebi.ac.uk/efo/EFO_0801667 GCST90241377 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hematopoietic prostaglandin D synthase levels (HPGDS.12549.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 hematopoietic prostaglandin D synthase measurement http://www.ebi.ac.uk/efo/EFO_0801668 GCST90241378 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heme oxygenase 2 levels (HMOX2.2622.18.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 heme oxygenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020436 GCST90241379 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HemK methyltransferase family member 2 levels (N6AMT1.11096.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 hemK methyltransferase family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0021891 GCST90241380 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hemoglobin subunit gamma-1 levels (HBG1.10665.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hemoglobin subunit gamma-1 measurement http://www.ebi.ac.uk/efo/EFO_0802590 GCST90241381 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hemoglobin subunit theta-1 levels (HBQ1.7965.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 hemoglobin subunit theta-1 measurement http://www.ebi.ac.uk/efo/EFO_0801669 GCST90241382 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hemoglobin subunit zeta levels (HBZ.6919.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 hemoglobin subunit zeta measurement http://www.ebi.ac.uk/efo/EFO_0801670 GCST90241383 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hemojuvelin levels (HFE2.3332.57.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 hemojuvelin measurement http://www.ebi.ac.uk/efo/EFO_0008148 GCST90241384 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HEPACAM family member 2 levels (HEPACAM2.6568.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 HEPACAM family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802591 GCST90241385 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HEPACAM family member 2 levels (HEPACAM2.9116.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 HEPACAM family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802591 GCST90241386 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heparan sulfate glucosamine 3-O-sulfotransferase 3A1 levels (HS3ST3A1.8268.98.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 heparan sulfate glucosamine 3-O-sulfotransferase 3A1 measurement http://www.ebi.ac.uk/efo/EFO_0801671 GCST90241387 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heparan sulfate glucosamine 3-O-sulfotransferase 3B1 levels (HS3ST3B1.6986.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heparan sulfate glucosamine 3-O-sulfotransferase 3B1 measurement http://www.ebi.ac.uk/efo/EFO_0802592 GCST90241388 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heparan sulfate glucosamine 3-O-sulfotransferase 4 levels (HS3ST4.8998.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heparan sulfate glucosamine 3-O-sulfotransferase 4 measurement http://www.ebi.ac.uk/efo/EFO_0802593 GCST90241389 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heparan-sulfate 6-O-sulfotransferase 1 levels (HS6ST1.5465.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 heparan-sulfate 6-o-sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020437 GCST90241390 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heparan-sulfate 6-O-sulfotransferase 2 levels (HS6ST2.13524.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heparan-sulfate 6-O-sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802594 GCST90241391 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heparin-binding EGF-like growth factor levels (HBEGF.14094.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 heparin-binding egf-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020438 GCST90241392 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heparin-binding EGF-like growth factor levels (HBEGF.4134.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heparin-binding egf-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020438 GCST90241393 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatitis A virus cellular receptor 1 levels (HAVCR1.9021.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 hepatitis A virus cellular receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010601 GCST90241394 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatitis A virus cellular receptor 2 levels (HAVCR2.5134.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90241395 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatitis A virus cellular receptor 2 levels (HAVCR2.7152.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90241396 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatocyte nuclear factor 4-alpha levels (HNF4A.10041.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 hepatocyte nuclear factor 4-alpha measurement http://www.ebi.ac.uk/efo/EFO_0801672 GCST90241401 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatoma-derived growth factor-related protein 2 levels (HDGFRP2.4553.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hepatoma-derived growth factor-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020439 GCST90241402 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoprotein A/B levels (HNRNPAB.8894.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heterogeneous nuclear ribonucleoprotein a/b measurement http://www.ebi.ac.uk/efo/EFO_0020441 GCST90241407 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoprotein M levels (HNRNPM.12783.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 heterogeneous nuclear ribonucleoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0801674 GCST90241410 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoproteins A2/B1 levels (HNRNPA2B1.5351.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 heterogeneous nuclear ribonucleoproteins A2/B1 measurement http://www.ebi.ac.uk/efo/EFO_0020444 GCST90241412 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hexokinase-1 levels (HK1.13131.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 hexokinase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021939 GCST90241414 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hexokinase-2 levels (HK2.13130.150.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 hexokinase-2 measurement http://www.ebi.ac.uk/efo/EFO_0021938 GCST90241415 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A levels (PDE7A.5178.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7a measurement http://www.ebi.ac.uk/efo/EFO_0020445 GCST90241416 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A levels (PDE9A.5201.50.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 high affinity cgmp-specific 3',5'-cyclic phosphodiesterase 9a measurement http://www.ebi.ac.uk/efo/EFO_0020446 GCST90241417 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High affinity immunoglobulin alpha and immunoglobulin mu Fc receptor levels (FCAMR.9568.289.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 high affinity immunoglobulin alpha and immunoglobulin mu Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0802598 GCST90241418 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High affinity immunoglobulin gamma Fc receptor I levels (FCGR1A.3312.64.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 high affinity immunoglobulin gamma fc receptor i measurement http://www.ebi.ac.uk/efo/EFO_0020447 GCST90241419 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High affinity nerve growth factor receptor levels (NTRK1.3477.63.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 high affinity nerve growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020448 GCST90241420 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High mobility group protein 20A levels (HMG20A.12712.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 high mobility group protein 20A measurement http://www.ebi.ac.uk/efo/EFO_0802599 GCST90241421 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High mobility group protein B1 levels (HMGB1.2524.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 high mobility group protein B1 measurement http://www.ebi.ac.uk/efo/EFO_0020449 GCST90241422 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High mobility group protein B2 levels (HMGB2.6913.189.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 high mobility group protein B2 measurement http://www.ebi.ac.uk/efo/EFO_0801676 GCST90241423 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. High mobility group protein B3 levels (HMGB3.12775.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 high mobility group protein B3 measurement http://www.ebi.ac.uk/efo/EFO_0801677 GCST90241424 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histatin-1 levels (HTN1.10608.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 histatin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801678 GCST90241425 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histidine triad nucleotide-binding protein 1 levels (HINT1.5900.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 histidine triad nucleotide-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020450 GCST90241426 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histidine triad nucleotide-binding protein 2, mitochondrial levels (HINT2.5612.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histidine triad nucleotide-binding protein 2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802600 GCST90241427 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histo-blood group ABO system transferase levels (ABO.9253.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 histo-blood group ABO system transferase measurement http://www.ebi.ac.uk/efo/EFO_0801679 GCST90241428 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone acetyltransferase KAT6A levels (KAT6A.2865.77.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 histone acetyltransferase kat6a measurement http://www.ebi.ac.uk/efo/EFO_0020451 GCST90241429 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone acetyltransferase type B catalytic subunit levels (HAT1.2858.29.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone acetyltransferase type b catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0020452 GCST90241430 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone deacetylase 8 levels (HDAC8.2859.69.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone deacetylase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020453 GCST90241431 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone deacetylase complex subunit SAP18 levels (SAP18.12830.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 histone deacetylase complex subunit SAP18 measurement http://www.ebi.ac.uk/efo/EFO_0801680 GCST90241432 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone deacetylase complex subunit SAP30 levels (SAP30.12888.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone deacetylase complex subunit SAP30 measurement http://www.ebi.ac.uk/efo/EFO_0802601 GCST90241433 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone H1.2 levels (HIST1H1C.2987.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone H1.2 measurement http://www.ebi.ac.uk/efo/EFO_0021966 GCST90241434 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone H1x levels (H1FX.12709.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 histone H1x measurement http://www.ebi.ac.uk/efo/EFO_0801681 GCST90241435 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone H2A deubiquitinase MYSM1 levels (MYSM1.11536.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone H2A deubiquitinase MYSM1 measurement http://www.ebi.ac.uk/efo/EFO_0802602 GCST90241436 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone H2A type 3 levels (HIST3H2A.14144.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone H2A type 3 measurement http://www.ebi.ac.uk/efo/EFO_0021953 GCST90241437 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone H2A.z levels (H2AFZ.4163.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone H2A.Z measurement http://www.ebi.ac.uk/efo/EFO_0020454 GCST90241438 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone-lysine N-methyltransferase 2C levels (KMT2C.11402.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 histone-lysine N-methyltransferase 2C measurement http://www.ebi.ac.uk/efo/EFO_0801682 GCST90241439 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone-lysine N-methyltransferase 2D levels (MLL2.13623.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 histone-lysine N-methyltransferase 2D measurement http://www.ebi.ac.uk/efo/EFO_0801683 GCST90241440 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone-lysine N-methyltransferase ASH1L levels (ASH1L.12622.96.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone-lysine N-methyltransferase ASH1L measurement http://www.ebi.ac.uk/efo/EFO_0802603 GCST90241441 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone-lysine N-methyltransferase EHMT2 levels (EHMT2.5843.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 histone-lysine n-methyltransferase EHMT2 measurement http://www.ebi.ac.uk/efo/EFO_0020455 GCST90241442 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone-lysine N-methyltransferase SETD2 levels (SETD2.12647.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone-lysine N-methyltransferase SETD2 measurement http://www.ebi.ac.uk/efo/EFO_0802604 GCST90241443 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone-lysine N-methyltransferase SETMAR levels (SETMAR.12462.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone-lysine N-methyltransferase SETMAR measurement http://www.ebi.ac.uk/efo/EFO_0802605 GCST90241444 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Histone-lysine N-methyltransferase SUV420H2 levels (SUV420H2.12452.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 histone-lysine N-methyltransferase SUV420H2 measurement http://www.ebi.ac.uk/efo/EFO_0802606 GCST90241445 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HLA class II histocompatibility antigen gamma chain levels (CD74.8748.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 HLA class II histocompatibility antigen gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0802607 GCST90241446 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin J chain levels (IGJ.8362.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin J chain measurement http://www.ebi.ac.uk/efo/EFO_0802620 GCST90241472 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin lambda-like polypeptide 1 levels (IGLL1.6485.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 immunoglobulin lambda-like polypeptide 1 measurement http://www.ebi.ac.uk/efo/EFO_0801688 GCST90241473 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin superfamily containing leucine-rich repeat protein 2 levels (ISLR2.13124.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 immunoglobulin superfamily containing leucine-rich repeat protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021879 GCST90241474 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin superfamily DCC subclass member 3 levels (IGDCC3.11952.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 immunoglobulin superfamily DCC subclass member 3 measurement http://www.ebi.ac.uk/efo/EFO_0801689 GCST90241475 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin superfamily DCC subclass member 3 levels (IGDCC3.7118.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin superfamily DCC subclass member 3 measurement http://www.ebi.ac.uk/efo/EFO_0801689 GCST90241476 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin superfamily DCC subclass member 4 levels (IGDCC4.9793.145.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 immunoglobulin superfamily DCC subclass member 4 measurement http://www.ebi.ac.uk/efo/EFO_0801690 GCST90241477 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin superfamily member 11 levels (IGSF11.9279.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0802621 GCST90241478 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin superfamily member 11 levels (IGSF11.10700.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0802621 GCST90241479 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Immunoglobulin superfamily member 8 levels (IGSF8.6984.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0802622 GCST90241480 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-1A levels (STX1A.3766.51.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 syntaxin-1a measurement http://www.ebi.ac.uk/efo/EFO_0020759 GCST90242946 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-1B levels (STX1B.6966.144.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 syntaxin-1B measurement http://www.ebi.ac.uk/efo/EFO_0803125 GCST90242947 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-2 levels (STX2.7738.299.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 syntaxin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802111 GCST90242948 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-6 levels (STX6.10945.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 syntaxin-6 measurement http://www.ebi.ac.uk/efo/EFO_0803126 GCST90242949 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-7 levels (STX7.8274.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 syntaxin-7 measurement http://www.ebi.ac.uk/efo/EFO_0802112 GCST90242950 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-8 levels (STX8.10903.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 syntaxin-8 measurement http://www.ebi.ac.uk/efo/EFO_0802113 GCST90242951 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-box transcription factor TBX22 levels (TBX22.11146.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-box transcription factor TBX22 measurement http://www.ebi.ac.uk/efo/EFO_0803127 GCST90242952 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-box transcription factor TBX3 levels (TBX3.13978.122.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-box transcription factor TBX3 measurement http://www.ebi.ac.uk/efo/EFO_0803128 GCST90242953 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-box transcription factor TBX5 levels (TBX5.11202.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-box transcription factor TBX5 measurement http://www.ebi.ac.uk/efo/EFO_0803129 GCST90242954 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell immunomodulatory protein levels (ITFG1.9347.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-cell immunomodulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0803130 GCST90242955 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell receptor-associated transmembrane adapter 1 levels (TRAT1.7224.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-cell receptor-associated transmembrane adapter 1 measurement http://www.ebi.ac.uk/efo/EFO_0803131 GCST90242956 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell surface antigen CD2 levels (CD2.7100.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-cell surface antigen CD2 measurement http://www.ebi.ac.uk/efo/EFO_0803132 GCST90242957 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell surface glycoprotein CD3 epsilon chain levels (CD3E.8069.85.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 T-cell surface glycoprotein CD3 epsilon chain measurement http://www.ebi.ac.uk/efo/EFO_0802114 GCST90242958 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell surface glycoprotein CD3 gamma chain levels (CD3G.7924.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-cell surface glycoprotein CD3 gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0803133 GCST90242959 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell surface glycoprotein CD4 levels (CD4.3143.3.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-cell surface glycoprotein CD4 measurement http://www.ebi.ac.uk/efo/EFO_0020760 GCST90242960 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. T-cell surface glycoprotein CD5 levels (CD5.14065.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 t-cell surface glycoprotein CD5 measurement http://www.ebi.ac.uk/efo/EFO_0803134 GCST90242961 Genome-wide genotyping array 2022-01-21 33763119 Read RW 2021-03-02 Front Genet www.ncbi.nlm.nih.gov/pubmed/33763119 Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. Triglyceride levels 9,183 European ancestry individuals 35,321 European ancestry individuals NR [5712318] 12 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90093142 Exome-wide sequencing 2022-08-31 35701560 Dofuku S 2022-06-14 Transl Stroke Res www.ncbi.nlm.nih.gov/pubmed/35701560 Genome-Wide Association Study of Intracranial Artery Stenosis Followed by Phenome-Wide Association Study. Intracranial artery stenosis 388 Japanese ancestry cases, 327 Japanese ancestry controls NA Illumina [NR] (imputed) 1 Arterial stenosis http://purl.obolibrary.org/obo/HP_0100545 GCST90133512 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Basigin levels (BSG.3585.54.6) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 basigin measurement http://www.ebi.ac.uk/efo/EFO_0020176 GCST90240381 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bcl-2-like protein 1 levels (BCL2L1.4423.77.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 BCL-2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020177 GCST90240382 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bcl-2-like protein 2 levels (BCL2L2.13097.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bcl-2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021928 GCST90240383 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bcl-2-like protein 2 levels (BCL2L2.7134.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bcl-2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021928 GCST90240384 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bcl-2-related protein A1 levels (BCL2A1.3413.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BCL-2-related protein A1 measurement http://www.ebi.ac.uk/efo/EFO_0020178 GCST90240385 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bcl10-interacting CARD protein levels (C9orf89.7778.104.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 bcl10-interacting CARD protein measurement http://www.ebi.ac.uk/efo/EFO_0801406 GCST90240386 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bcl2-associated agonist of cell death levels (BAD.5870.23.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bcl2-associated agonist of cell death measurement http://www.ebi.ac.uk/efo/EFO_0021998 GCST90240387 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 levels (BNIP3.7045.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802304 GCST90240388 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BCL2/adenovirus E1B 19 kDa protein-interacting protein 3-like levels (BNIP3L.7835.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BCL2/adenovirus E1B 19 kDa protein-interacting protein 3-like measurement http://www.ebi.ac.uk/efo/EFO_0802305 GCST90240389 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BDNF/NT-3 growth factors receptor levels (NTRK2.4866.59.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bdnf/nt-3 growth factors receptor measurement http://www.ebi.ac.uk/efo/EFO_0020179 GCST90240390 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beclin-1 levels (BECN1.13032.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beclin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802306 GCST90240391 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BET1-like protein levels (BET1L.10959.125.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BET1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802307 GCST90240392 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase levels (GCNT1.7016.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802308 GCST90240393 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 levels (GCNT4.10854.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 measurement http://www.ebi.ac.uk/efo/EFO_0801407 GCST90240394 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 levels (GCNT4.10842.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 measurement http://www.ebi.ac.uk/efo/EFO_0801407 GCST90240395 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,3-galactosyltransferase 6 levels (B3GALT6.7981.230.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,3-galactosyltransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0802309 GCST90240396 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,3-glucosyltransferase levels (B3GALTL.5727.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,3-glucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802310 GCST90240397 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,3-N-acetylglucosaminyltransferase manic fringe levels (MFNG.5605.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,3-N-acetylglucosaminyltransferase manic fringe measurement http://www.ebi.ac.uk/efo/EFO_0802311 GCST90240398 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,3-N-acetylglucosaminyltransferase radical fringe levels (RFNG.7203.125.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-1,3-N-acetylglucosaminyltransferase radical fringe measurement http://www.ebi.ac.uk/efo/EFO_0801408 GCST90240399 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,4-galactosyltransferase 1 levels (B4GALT1.13381.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 beta-1,4-galactosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801409 GCST90240400 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,4-galactosyltransferase 2 levels (B4GALT2.9595.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-1,4-galactosyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801410 GCST90240401 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,4-galactosyltransferase 3 levels (B4GALT3.6921.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,4-galactosyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802312 GCST90240402 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,4-galactosyltransferase 5 levels (B4GALT5.10425.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,4-galactosyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0802313 GCST90240403 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,4-galactosyltransferase 6 levels (B4GALT6.10832.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 beta-1,4-galactosyltransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0801411 GCST90240404 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,4-galactosyltransferase 7 levels (B4GALT7.7806.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-1,4-galactosyltransferase 7 measurement http://www.ebi.ac.uk/efo/EFO_0802314 GCST90240405 Genome-wide genotyping array 2022-02-07 34125832 Borda V 2021-06-14 PLoS Negl Trop Dis www.ncbi.nlm.nih.gov/pubmed/34125832 Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome. Congenital Zika syndrome 29 Hispanic or Latin American cases, 11 Hispanic or Latin American controls NA NR [144153] 1 Zika virus congenital syndrome http://purl.obolibrary.org/obo/MONDO_0000890 GCST90093463 Exome-wide sequencing 2022-03-21 34743218 Drake I 2021-11-07 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34743218 The role of circulating galectin-1 in type 2 diabetes and chronic kidney disease: evidence from cross-sectional, longitudinal and Mendelian randomisation analyses. Galectin-1 levels 4,086 individuals NA Illumina [21575257] (imputed) 1 galectin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020932 GCST90095191 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chorionic somatomammotropin hormone levels (CSH1.CSH2.13103.125.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chorionic somatomammotropin hormone measurement http://www.ebi.ac.uk/efo/EFO_0021929 GCST90240695 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chromobox protein homolog 5 levels (CBX5.4540.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 chromobox protein homolog 5 measurement http://www.ebi.ac.uk/efo/EFO_0020258 GCST90240696 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chromobox protein homolog 7 levels (CBX7.13027.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 chromobox protein homolog 7 measurement http://www.ebi.ac.uk/efo/EFO_0801475 GCST90240697 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chromodomain-helicase-DNA-binding protein 7 levels (CHD7.14005.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chromodomain-helicase-DNA-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802397 GCST90240698 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chromogranin-A levels (CHGA.8476.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 chromogranin-A measurement http://www.ebi.ac.uk/efo/EFO_0022021 GCST90240699 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chymase levels (CMA1.3423.59.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chymase measurement http://www.ebi.ac.uk/efo/EFO_0020259 GCST90240700 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chymotrypsin-C levels (CTRC.5626.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chymotrypsin-C measurement http://www.ebi.ac.uk/efo/EFO_0802398 GCST90240701 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chymotrypsin-like elastase family member 2A levels (CELA2A.7140.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chymotrypsin-like elastase family member 2A measurement http://www.ebi.ac.uk/efo/EFO_0802399 GCST90240702 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chymotrypsin-like elastase family member 3B levels (CELA3B.6357.83.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chymotrypsin-like elastase family member 3B measurement http://www.ebi.ac.uk/efo/EFO_0802400 GCST90240703 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chymotrypsin-like protease CTRL-1 levels (CTRL.9229.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 chymotrypsin-like protease CTRL-1 measurement http://www.ebi.ac.uk/efo/EFO_0801476 GCST90240704 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chymotrypsinogen B levels (CTRB1.5671.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 chymotrypsinogen B measurement http://www.ebi.ac.uk/efo/EFO_0801477 GCST90240705 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cilia- and flagella-associated protein 45 levels (CFAP45.6553.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cilia- and flagella-associated protein 45 measurement http://www.ebi.ac.uk/efo/EFO_0802401 GCST90240706 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ciliary neurotrophic factor levels (CNTF.3489.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ciliary neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020260 GCST90240707 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ciliary neurotrophic factor receptor subunit alpha levels (CNTFR.14101.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ciliary neurotrophic factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020261 GCST90240708 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ciliary neurotrophic factor receptor subunit alpha levels (CNTFR.2711.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ciliary neurotrophic factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020261 GCST90240709 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ck-beta-8-1 levels (CCL23.3028.36.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 Ck-beta-8-1 measurement http://www.ebi.ac.uk/efo/EFO_0008085 GCST90240710 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Clathrin heavy chain 1 levels (CLTC.13711.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 clathrin heavy chain 1 measurement http://www.ebi.ac.uk/efo/EFO_0802402 GCST90240711 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Clathrin interactor 1 levels (CLINT1.11659.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 clathrin interactor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801478 GCST90240712 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Clusterin levels (CLU.4542.24.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007655 GCST90240713 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1 levels (ST3GAL1.5657.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801479 GCST90240714 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2 levels (ST3GAL2.6281.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802403 GCST90240715 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase levels (ST8SIA4.7038.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802404 GCST90240716 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMRF35-like molecule 1 levels (CD300LF.5623.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CMRF35-like molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0802405 GCST90240717 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMRF35-like molecule 2 levels (CD300E.10798.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CMRF35-like molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0802406 GCST90240718 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMRF35-like molecule 6 levels (CD300C.5066.134.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90240719 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ceramide synthase 5 levels (CERS5.13494.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ceramide synthase 5 measurement http://www.ebi.ac.uk/efo/EFO_0802388 GCST90240671 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cerebellin-1 levels (CBLN1.9313.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 cerebellin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801466 GCST90240672 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cerebellin-4 levels (CBLN4.5688.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cerebellin-4 measurement http://www.ebi.ac.uk/efo/EFO_0801467 GCST90240673 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cerebral cavernous malformations 2 protein levels (CCM2.12347.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cerebral cavernous malformations 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0802389 GCST90240674 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cerebral dopamine neurotrophic factor levels (CDNF.4962.52.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90240675 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ceroid-lipofuscinosis neuronal protein 5 levels (CLN5.8874.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ceroid-lipofuscinosis neuronal protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802390 GCST90240676 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ceroid-lipofuscinosis neuronal protein 5 levels (CLN5.9795.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ceroid-lipofuscinosis neuronal protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802390 GCST90240677 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cGMP-dependent 3',5'-cyclic phosphodiesterase levels (PDE2A.5246.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cGMP-dependent 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0802391 GCST90240678 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cGMP-dependent protein kinase 1, beta isozyme levels (PRKG1.13067.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cGMP-dependent protein kinase 1, beta isozyme measurement http://www.ebi.ac.uk/efo/EFO_0801468 GCST90240679 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cGMP-inhibited 3',5'-cyclic phosphodiesterase A levels (PDE3A.5254.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cGMP-inhibited 3',5'-cyclic phosphodiesterase A measurement http://www.ebi.ac.uk/efo/EFO_0020255 GCST90240680 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Charged multivesicular body protein 3 levels (VPS24.12508.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 charged multivesicular body protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801469 GCST90240681 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chitinase-3-like protein 1 levels (CHI3L1.11104.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 chitinase-3-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801470 GCST90240682 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chitinase-3-like protein 2 levels (CHI3L2.9383.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 chitinase-3-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801471 GCST90240683 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chitotriosidase-1 levels (CHIT1.3600.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90240684 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chloride intracellular channel protein 4 levels (CLIC4.12491.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chloride intracellular channel protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802392 GCST90240685 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chloride intracellular channel protein 5 levels (CLIC5.12475.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 chloride intracellular channel protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801472 GCST90240686 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Choline/ethanolamine kinase levels (CHKB.13117.232.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 choline/ethanolamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0021935 GCST90240687 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chondroadherin levels (CHAD.13460.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chondroadherin measurement http://www.ebi.ac.uk/efo/EFO_0802393 GCST90240688 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium/calmodulin-dependent protein kinase type 1D levels (CAMK1D.3418.12.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90240556 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chondroitin sulfate N-acetylgalactosaminyltransferase 2 levels (CSGALNACT2.10772.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 chondroitin sulfate N-acetylgalactosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801473 GCST90240689 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chondroitin sulfate proteoglycan 4 levels (CSPG4.8951.162.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chondroitin sulfate proteoglycan 4 measurement http://www.ebi.ac.uk/efo/EFO_0802394 GCST90240690 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chordin levels (CHRD.13438.115.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chordin measurement http://www.ebi.ac.uk/efo/EFO_0802395 GCST90240691 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chordin-like protein 1 levels (CHRDL1.3362.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 chordin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020257 GCST90240692 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Chordin-like protein 2 levels (CHRDL2.6086.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 chordin-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801474 GCST90240693 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Choriogonadotropin subunit beta variant 2 levels (CGB2.6213.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 choriogonadotropin subunit beta variant 2 measurement http://www.ebi.ac.uk/efo/EFO_0802396 GCST90240694 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Annexin A10 levels (ANXA10.13605.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 annexin A10 measurement http://www.ebi.ac.uk/efo/EFO_0801383 GCST90240297 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Annexin A2 levels (ANXA2.13700.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 annexin A2 measurement http://www.ebi.ac.uk/efo/EFO_0008027 GCST90240298 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Annexin A2 levels (ANXA2.4961.17.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 annexin A2 measurement http://www.ebi.ac.uk/efo/EFO_0008027 GCST90240299 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Annexin A9 levels (ANXA9.13588.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 annexin A9 measurement http://www.ebi.ac.uk/efo/EFO_0802283 GCST90240300 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Anosmin-1 levels (KAL1.6603.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 anosmin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802284 GCST90240301 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Anterior gradient protein 2 homolog levels (AGR2.4959.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 anterior gradient protein 2 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020152 GCST90240302 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Antigen-presenting glycoprotein CD1d levels (CD1D.8749.194.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 antigen-presenting glycoprotein CD1d measurement http://www.ebi.ac.uk/efo/EFO_0802285 GCST90240303 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Antithrombin-III levels (SERPINC1.3344.60.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 antithrombin-III measurement http://www.ebi.ac.uk/efo/EFO_0020155 GCST90240304 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. AP-4 complex accessory subunit tepsin levels (ENTHD2.7947.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 AP-4 complex accessory subunit tepsin measurement http://www.ebi.ac.uk/efo/EFO_0801384 GCST90240305 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. AP-4 complex subunit mu-1 levels (AP4M1.10076.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 AP-4 complex subunit mu-1 measurement http://www.ebi.ac.uk/efo/EFO_0801385 GCST90240306 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. APOBEC1 complementation factor levels (A1CF.12423.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 APOBEC1 complementation factor measurement http://www.ebi.ac.uk/efo/EFO_0801386 GCST90240307 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein A-V levels (APOA5.12908.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 apolipoprotein A-V measurement http://www.ebi.ac.uk/efo/EFO_0801387 GCST90240308 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein A-V levels (APOA5.11318.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 apolipoprotein A-V measurement http://www.ebi.ac.uk/efo/EFO_0801387 GCST90240309 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein B levels (APOB.2797.56.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90240310 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein D levels (APOD.4712.28.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90240311 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein D levels (APOD.8262.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90240312 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein E (isoform E2) levels (APOE.5312.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 apolipoprotein E isoform E2 measurement http://www.ebi.ac.uk/efo/EFO_0008028 GCST90240313 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein E (isoform E3) levels (APOE.2937.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 apolipoprotein E (isoform E3) measurement http://www.ebi.ac.uk/efo/EFO_0020157 GCST90240314 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein F levels (APOF.12370.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 apolipoprotein F measurement http://www.ebi.ac.uk/efo/EFO_0801388 GCST90240315 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein L1 levels (APOL1.9506.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90240316 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein L1 levels (APOL1.11510.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90240317 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein M levels (APOM.10445.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 apolipoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0021945 GCST90240318 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apolipoprotein M levels (APOM.14125.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 apolipoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0021945 GCST90240319 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apoptosis regulator Bcl-2 levels (BCL2.3412.7.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 apoptosis regulator BCL-2 measurement http://www.ebi.ac.uk/efo/EFO_0020159 GCST90240320 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apoptosis-inducing factor 1, mitochondrial levels (AIFM1.13424.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 apoptosis-inducing factor 1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801389 GCST90240321 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMRF35-like molecule 6 levels (CD300C.13406.161.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90240720 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMRF35-like molecule 7 levels (CD300LB.10713.151.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CMRF35-like molecule 7 measurement http://www.ebi.ac.uk/efo/EFO_0802407 GCST90240721 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMRF35-like molecule 8 levels (CD300A.5630.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 CMRF35-like molecule 8 measurement http://www.ebi.ac.uk/efo/EFO_0801480 GCST90240722 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CMRF35-like molecule 9 levels (CD300LG.9909.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CMRF35-like molecule 9 measurement http://www.ebi.ac.uk/efo/EFO_0802408 GCST90240723 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coactosin-like protein levels (COTL1.4905.63.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coactosin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020262 GCST90240724 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coagulation Factor VIII levels (F8.13499.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 factor VIII measurement http://www.ebi.ac.uk/efo/EFO_0004630 GCST90240725 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coagulation Factor X levels (F10.4878.3.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 coagulation factor X measurement http://www.ebi.ac.uk/efo/EFO_0020265 GCST90240726 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coagulation factor Xa levels (F10.3077.66.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 coagulation factor XA measurement http://www.ebi.ac.uk/efo/EFO_0020266 GCST90240727 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cocaine- and amphetamine-regulated transcript protein levels (CARTPT.5743.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cocaine- and amphetamine-regulated transcript protein measurement http://www.ebi.ac.uk/efo/EFO_0802409 GCST90240728 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cochlin levels (COCH.7227.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 cochlin measurement http://www.ebi.ac.uk/efo/EFO_0801481 GCST90240729 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cofilin-1 levels (CFL1.4203.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 cofilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020267 GCST90240730 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil domain-containing protein 126 levels (CCDC126.6388.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 coiled-coil domain-containing protein 126 measurement http://www.ebi.ac.uk/efo/EFO_0801482 GCST90240731 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil domain-containing protein 134 levels (CCDC134.5587.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coiled-coil domain-containing protein 134 measurement http://www.ebi.ac.uk/efo/EFO_0802410 GCST90240732 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil domain-containing protein 167 levels (CCDC167.7797.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coiled-coil domain-containing protein 167 measurement http://www.ebi.ac.uk/efo/EFO_0802411 GCST90240733 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil domain-containing protein 51 levels (CCDC51.12790.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coiled-coil domain-containing protein 51 measurement http://www.ebi.ac.uk/efo/EFO_0802412 GCST90240734 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil domain-containing protein 80 levels (CCDC80.3234.23.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coiled-coil domain-containing protein 80 measurement http://www.ebi.ac.uk/efo/EFO_0020268 GCST90240735 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil domain-containing protein 90B, mitochondrial levels (CCDC90B.7792.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coiled-coil domain-containing protein 90B, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802413 GCST90240736 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial levels (CHCHD10.11270.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801483 GCST90240737 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coiled-coil-helix-coiled-coil-helix domain-containing protein 2 levels (CHCHD2.8015.144.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coiled-coil-helix-coiled-coil-helix domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802414 GCST90240738 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cold shock domain-containing protein C2 levels (CSDC2.12754.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cold shock domain-containing protein C2 measurement http://www.ebi.ac.uk/efo/EFO_0802415 GCST90240739 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cold shock domain-containing protein E1 levels (CSDE1.12735.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cold shock domain-containing protein E1 measurement http://www.ebi.ac.uk/efo/EFO_0802416 GCST90240740 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cold-inducible RNA-binding protein levels (CIRBP.12724.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cold-inducible RNA-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801484 GCST90240741 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Colipase levels (CLPS.5749.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 colipase measurement http://www.ebi.ac.uk/efo/EFO_0801485 GCST90240742 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Colipase-like protein 2 levels (CLPSL2.7767.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 colipase-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802417 GCST90240743 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-1(I) chain levels (COL1A1.11140.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 collagen alpha-1(I) chain measurement http://www.ebi.ac.uk/efo/EFO_0801486 GCST90240744 Genome-wide genotyping array 2022-03-25 34782459 Shevchenko AK 2021-11-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/34782459 Genome-wide association study reveals genetic variants associated with HIV-1C infection in a Botswana study population. HIV-1 susceptibility 194 Sub-Saharan African ancestry cases, 236 Sub-Saharan African ancestry controls NA Illumina [1374256] 0 HIV infection http://www.ebi.ac.uk/efo/EFO_0000764 GCST90096801 Genome-wide genotyping array 2022-03-25 34782459 Shevchenko AK 2021-11-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/34782459 Genome-wide association study reveals genetic variants associated with HIV-1C infection in a Botswana study population. HIV-1 susceptibility 256 Sub-Saharan African ancestry cases, 80 Sub-Saharan African ancestry controls NA NR [8636400] 2 HIV infection http://www.ebi.ac.uk/efo/EFO_0000764 GCST90096802 Genome-wide sequencing 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial levels (NDUFV2.7748.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802785 GCST90242028 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial levels (NDUFS4.10584.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0803292 GCST90242029 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NADH-cytochrome b5 reductase 3 levels (CYB5R3.7215.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NADH-cytochrome b5 reductase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802786 GCST90242030 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NADPH--cytochrome P450 reductase levels (POR.2731.29.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NADPH--cytochrome P450 reductase measurement http://www.ebi.ac.uk/efo/EFO_0008242 GCST90242031 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Natural cytotoxicity triggering receptor 1 levels (NCR1.8360.169.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90242032 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Natural cytotoxicity triggering receptor 1 levels (NCR1.5104.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90242033 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Natural cytotoxicity triggering receptor 2 levels (NCR2.2734.49.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 natural cytotoxicity triggering receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020589 GCST90242034 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Natural cytotoxicity triggering receptor 3 levels (NCR3.3003.29.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 natural cytotoxicity triggering receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008243 GCST90242035 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Natural cytotoxicity triggering receptor 3 ligand 1 levels (NCR3LG1.7854.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 natural cytotoxicity triggering receptor 3 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0802787 GCST90242036 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nectin-2 levels (PVRL2.6245.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802788 GCST90242037 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nectin-3 levels (PVRL3.13557.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802789 GCST90242038 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nectin-4 levels (PVRL4.5734.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802790 GCST90242039 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neogenin levels (NEO1.8900.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neogenin measurement http://www.ebi.ac.uk/efo/EFO_0801823 GCST90242040 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nesprin-2 levels (SYNE2.9789.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nesprin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801824 GCST90242041 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin receptor UNC5A levels (UNC5A.7975.97.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 netrin receptor UNC5A measurement http://www.ebi.ac.uk/efo/EFO_0802791 GCST90242042 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin receptor UNC5B levels (UNC5B.7776.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 netrin receptor UNC5B measurement http://www.ebi.ac.uk/efo/EFO_0802792 GCST90242043 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin receptor UNC5C levels (UNC5C.5139.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 netrin receptor UNC5C measurement http://www.ebi.ac.uk/efo/EFO_0020590 GCST90242044 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin receptor UNC5D levels (UNC5D.5140.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90242045 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin receptor UNC5D levels (UNC5D.8624.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90242046 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin-1 levels (NTN1.6649.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 netrin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022009 GCST90242047 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin-1 levels (NTN1.6634.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 netrin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022009 GCST90242048 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin-4 levels (NTN4.3327.27.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 netrin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020592 GCST90242049 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Netrin-G1 levels (NTNG1.5637.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 netrin-G1 measurement http://www.ebi.ac.uk/efo/EFO_0801825 GCST90242050 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neudesin levels (NENF.9219.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neudesin measurement http://www.ebi.ac.uk/efo/EFO_0802793 GCST90242051 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neugrin levels (NGRN.7153.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neugrin measurement http://www.ebi.ac.uk/efo/EFO_0802794 GCST90242052 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MHC class I polypeptide-related sequence B levels (MICB.5102.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 10 MHC class I polypeptide-related sequence B measurement http://www.ebi.ac.uk/efo/EFO_0008234 GCST90241928 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MICAL-like protein 2 levels (MICALL2.12891.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 MICAL-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801799 GCST90241929 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MICOS complex subunit MIC10 levels (MINOS1.7956.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 MICOS complex subunit MIC10 measurement http://www.ebi.ac.uk/efo/EFO_0801800 GCST90241930 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MICOS complex subunit MIC26 levels (APOO.9373.405.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MICOS complex subunit MIC26 measurement http://www.ebi.ac.uk/efo/EFO_0802743 GCST90241931 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Microfibril-associated glycoprotein 4 levels (MFAP4.5636.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 microfibril-associated glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802744 GCST90241932 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Microfibrillar-associated protein 1 levels (MFAP1.5606.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 microfibrillar-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802745 GCST90241933 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Microfibrillar-associated protein 2 levels (MFAP2.9294.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 microfibrillar-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801801 GCST90241934 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Microfibrillar-associated protein 5 levels (MFAP5.6440.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 microfibrillar-associated protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802746 GCST90241935 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Midkine levels (MDK.2911.27.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 midkine measurement http://www.ebi.ac.uk/efo/EFO_0020571 GCST90241936 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mineralocorticoid receptor levels (NR3C2.12931.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mineralocorticoid receptor measurement http://www.ebi.ac.uk/efo/EFO_0801802 GCST90241937 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MIP18 family protein FAM96A levels (FAM96A.8787.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MIP18 family protein FAM96A measurement http://www.ebi.ac.uk/efo/EFO_0802747 GCST90241938 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mismatch repair endonuclease PMS2 levels (PMS2.11312.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mismatch repair endonuclease PMS2 measurement http://www.ebi.ac.uk/efo/EFO_0802748 GCST90241939 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitochondrial fission regulator 1 levels (MTFR1.9095.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitochondrial fission regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0802749 GCST90241940 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitochondrial glutamate carrier 2 levels (SLC25A18.5280.68.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitochondrial glutamate carrier 2 measurement http://www.ebi.ac.uk/efo/EFO_0020572 GCST90241941 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitochondrial import inner membrane translocase subunit TIM14 levels (DNAJC19.4545.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitochondrial import inner membrane translocase subunit tim14 measurement http://www.ebi.ac.uk/efo/EFO_0020573 GCST90241942 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitochondrial peptide methionine sulfoxide reductase levels (MSRA.7137.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitochondrial peptide methionine sulfoxide reductase measurement http://www.ebi.ac.uk/efo/EFO_0802750 GCST90241943 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitochondrial sodium/hydrogen exchanger 9B2 levels (SLC9B2.9088.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitochondrial sodium/hydrogen exchanger 9B2 measurement http://www.ebi.ac.uk/efo/EFO_0801803 GCST90241944 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitochondrial ubiquitin ligase activator of NFKB 1 levels (MUL1.9315.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 mitochondrial ubiquitin ligase activator of NFKB 1 measurement http://www.ebi.ac.uk/efo/EFO_0801804 GCST90241945 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitochondrial ubiquitin ligase activator of NFKB 1 levels (MUL1.11159.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitochondrial ubiquitin ligase activator of NFKB 1 measurement http://www.ebi.ac.uk/efo/EFO_0801804 GCST90241946 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitofusin-1 levels (MFN1.11364.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitofusin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802751 GCST90241947 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase 1 levels (MAPK1.3115.64.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitogen-activated protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020574 GCST90241948 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase 13 levels (MAPK13.5006.71.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 mitogen-activated protein kinase 13 measurement http://www.ebi.ac.uk/efo/EFO_0020577 GCST90241949 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase 14 levels (MAPK14.5007.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitogen-activated protein kinase 14 measurement http://www.ebi.ac.uk/efo/EFO_0020578 GCST90241950 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase 3 levels (MAPK3.2855.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitogen-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020579 GCST90241951 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase 8 levels (MAPK8.3825.18.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitogen-activated protein kinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020580 GCST90241952 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase 9 levels (MAPK9.5244.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitogen-activated protein kinase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020581 GCST90241953 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase kinase kinase 3 levels (MAP3K3.12990.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitogen-activated protein kinase kinase kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801805 GCST90241954 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitogen-activated protein kinase kinase kinase 7:TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 fusion levels (MAP3K7.TAB1.5259.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitogen-activated protein kinase kinase kinase 7:tgf-beta-activated kinase 1 and map3k7-binding protein 1 fusion measurement http://www.ebi.ac.uk/efo/EFO_0020582 GCST90241955 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitotic checkpoint serine/threonine-protein kinase BUB1 levels (BUB1.12033.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitotic checkpoint serine/threonine-protein kinase BUB1 measurement http://www.ebi.ac.uk/efo/EFO_0801806 GCST90241956 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitotic spindle assembly checkpoint protein MAD1 levels (MAD1L1.13618.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mitotic spindle assembly checkpoint protein MAD1 measurement http://www.ebi.ac.uk/efo/EFO_0801807 GCST90241957 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mitotic-spindle organizing protein 1 levels (MZT1.8072.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mitotic-spindle organizing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802752 GCST90241958 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MOB kinase activator 1A levels (MOB1A.12426.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MOB kinase activator 1A measurement http://www.ebi.ac.uk/efo/EFO_0802753 GCST90241959 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mono [ADP-ribose] polymerase PARP16 levels (PARP16.7881.244.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mono [ADP-ribose] polymerase PARP16 measurement http://www.ebi.ac.uk/efo/EFO_0803296 GCST90241960 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Monoacylglycerol lipase ABHD12 levels (ABHD12.7825.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 monoacylglycerol lipase ABHD12 measurement http://www.ebi.ac.uk/efo/EFO_0802754 GCST90241961 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mothers against decapentaplegic homolog 2 levels (SMAD2.10364.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mothers against decapentaplegic homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0021914 GCST90241962 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mothers against decapentaplegic homolog 4 levels (SMAD4.12022.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mothers against decapentaplegic homolog 4 measurement http://www.ebi.ac.uk/efo/EFO_0801808 GCST90241963 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Motor neuron and pancreas homeobox protein 1 levels (MNX1.9576.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 motor neuron and pancreas homeobox protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802755 GCST90241964 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. mRNA-capping enzyme levels (RNGTT.12847.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MRNA-capping enzyme measurement http://www.ebi.ac.uk/efo/EFO_0802756 GCST90241965 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. mRNA-decapping enzyme 1A levels (DCP1A.14008.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MRNA-decapping enzyme 1A measurement http://www.ebi.ac.uk/efo/EFO_0802757 GCST90241966 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mucin-1 levels (MUC1.9176.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90241967 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mucin-1 levels (MUC1.11267.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90241968 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mucin-4 levels (MUC4.10659.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mucin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802758 GCST90241969 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mucosal addressin cell adhesion molecule 1 levels (MADCAM1.11258.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mucosal addressin cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0802759 GCST90241970 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Muellerian-inhibiting factor levels (AMH.4923.79.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 muellerian-inhibiting factor measurement http://www.ebi.ac.uk/efo/EFO_0020584 GCST90241971 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multidrug resistance-associated protein 6 levels (ABCC6.8935.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 multidrug resistance-associated protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0802760 GCST90241972 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multifunctional protein ADE2 levels (PAICS.9841.197.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 multifunctional protein ADE2 measurement http://www.ebi.ac.uk/efo/EFO_0802761 GCST90241973 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multimerin-2 levels (MMRN2.11895.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 multimerin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801809 GCST90241974 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multimerin-2 levels (MMRN2.9723.105.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 multimerin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801809 GCST90241975 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multiple coagulation factor deficiency protein 2 levels (MCFD2.10476.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 multiple coagulation factor deficiency protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801810 GCST90241976 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multiple epidermal growth factor-like domains protein 10 levels (MEGF10.11168.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 multiple epidermal growth factor-like domains protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0802762 GCST90241977 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylgalactosaminyltransferase 7 levels (GALNT7.10888.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 n-acetylgalactosaminyltransferase 7 measurement http://www.ebi.ac.uk/efo/EFO_0802774 GCST90242003 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase levels (NAGPA.11208.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 n-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase measurement http://www.ebi.ac.uk/efo/EFO_0801816 GCST90242004 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylglucosamine-1-phosphotransferase subunit gamma levels (GNPTG.10666.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 n-acetylglucosamine-1-phosphotransferase subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0802775 GCST90242005 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylglucosamine-6-sulfatase levels (GNS.8314.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90242006 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylglucosamine-6-sulfatase levels (GNS.3616.3.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90242007 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylglutamate synthase, mitochondrial levels (NAGS.11247.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 n-acetylglutamate synthase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802776 GCST90242008 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 levels (B3GNT2.7980.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 n-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801817 GCST90242009 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase, isoform C levels (GCNT2.7143.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 n-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase, isoform C measurement http://www.ebi.ac.uk/efo/EFO_0802777 GCST90242010 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylserotonin O-methyltransferase-like protein levels (ASMTL.10089.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 n-acetylserotonin O-methyltransferase-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801818 GCST90242011 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetyltransferase 14 levels (NAT14.11120.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 n-acetyltransferase 14 measurement http://www.ebi.ac.uk/efo/EFO_0801819 GCST90242012 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acylethanolamine-hydrolyzing acid amidase levels (NAAA.3173.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90242013 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-lysine methyltransferase SMYD2 levels (SMYD2.12636.113.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 n-lysine methyltransferase SMYD2 measurement http://www.ebi.ac.uk/efo/EFO_0802778 GCST90242014 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-terminal pro-BNP levels (NPPB.7655.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 N-terminal pro-BNP measurement http://www.ebi.ac.uk/efo/EFO_0022014 GCST90242015 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-terminal Xaa-Pro-Lys N-methyltransferase 1 levels (NTMT1.12454.105.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 n-terminal Xaa-Pro-Lys N-methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801820 GCST90242016 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NA levels (NoneX.13231.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 immunoglobulin heavy constant gamma 4 measurement http://www.ebi.ac.uk/efo/EFO_0802779 GCST90242017 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NACHT, LRR and PYD domains-containing protein 1 levels (NLRP1.11661.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NACHT, LRR and PYD domains-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802780 GCST90242018 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NACHT, LRR and PYD domains-containing protein 10 levels (NLRP10.12821.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NACHT, LRR and PYD domains-containing protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0802781 GCST90242019 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NACHT, LRR and PYD domains-containing protein 4 levels (NLRP4.12794.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NACHT, LRR and PYD domains-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802782 GCST90242020 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NAD kinase levels (NADK.13624.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 NAD kinase measurement http://www.ebi.ac.uk/efo/EFO_0801821 GCST90242021 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NAD-dependent protein deacetylase sirtuin-2 levels (SIRT2.5030.52.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 NAD-dependent protein deacetylase sirtuin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008241 GCST90242022 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NAD-dependent protein deacylase sirtuin-5, mitochondrial levels (SIRT5.12461.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 NAD-dependent protein deacylase sirtuin-5, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801822 GCST90242023 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NAD(P)H dehydrogenase [quinone] 1 levels (NQO1.9837.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 NAD(P)H dehydrogenase [quinone] 1 measurement http://www.ebi.ac.uk/efo/EFO_0803303 GCST90242024 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial levels (NDUFB11.7747.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802783 GCST90242025 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4 levels (NDUFB4.10677.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0803307 GCST90242026 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 8, mitochondrial levels (NDUFB8.9800.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 8, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802784 GCST90242027 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multiple inositol polyphosphate phosphatase 1 levels (MINPP1.5586.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 multiple inositol polyphosphate phosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801811 GCST90241978 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Multiple PDZ domain protein levels (MPDZ.14036.116.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 multiple PDZ domain protein measurement http://www.ebi.ac.uk/efo/EFO_0802763 GCST90241979 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Muscle, skeletal receptor tyrosine-protein kinase levels (MUSK.11547.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 muscle, skeletal receptor tyrosine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0802764 GCST90241980 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myc box-dependent-interacting protein 1 levels (BIN1.9574.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myc box-dependent-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802765 GCST90241981 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myc proto-oncogene protein levels (MYC.10362.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myc proto-oncogene protein measurement http://www.ebi.ac.uk/efo/EFO_0021912 GCST90241982 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myc target protein 1 levels (MYCT1.13541.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 myc target protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801812 GCST90241983 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myc-associated zinc finger protein levels (MAZ.13436.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myc-associated zinc finger protein measurement http://www.ebi.ac.uk/efo/EFO_0802766 GCST90241984 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myelin protein P0 levels (MPZ.10615.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 myelin protein P0 measurement http://www.ebi.ac.uk/efo/EFO_0801813 GCST90241985 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myelin regulatory factor levels (MYRF.8843.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myelin regulatory factor measurement http://www.ebi.ac.uk/efo/EFO_0802767 GCST90241986 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myeloblastin levels (PRTN3.3514.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90241987 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myeloblastin levels (PRTN3.13720.95.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90241988 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myeloid cell surface antigen CD33 levels (CD33.3166.92.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90241989 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myeloid zinc finger 1 levels (MZF1.14662.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myeloid zinc finger 1 measurement http://www.ebi.ac.uk/efo/EFO_0802768 GCST90241990 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myeloperoxidase levels (MPO.2580.83.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90241991 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myocardial zonula adherens protein levels (MYZAP.13924.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myocardial zonula adherens protein measurement http://www.ebi.ac.uk/efo/EFO_0802769 GCST90241992 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myocardial zonula adherens protein levels (MYZAP.9055.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myocardial zonula adherens protein measurement http://www.ebi.ac.uk/efo/EFO_0802769 GCST90241993 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myocardial zonula adherens protein levels (MYZAP.9964.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myocardial zonula adherens protein measurement http://www.ebi.ac.uk/efo/EFO_0802769 GCST90241994 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myocyte-specific enhancer factor 2C levels (MEF2C.8933.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myocyte-specific enhancer factor 2C measurement http://www.ebi.ac.uk/efo/EFO_0802770 GCST90241995 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myoglobin levels (MB.3042.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myoglobin measurement http://www.ebi.ac.uk/efo/EFO_0005057 GCST90241996 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myomesin-2 levels (MYOM2.13534.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myomesin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802771 GCST90241997 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myosin-binding protein C, slow-type levels (MYBPC1.7648.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myosin-binding protein C, slow-type measurement http://www.ebi.ac.uk/efo/EFO_0802772 GCST90241998 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myotonin-protein kinase levels (DMPK.9010.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 myotonin-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0801814 GCST90241999 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Myotubularin-related protein 1 levels (MTMR1.11167.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 myotubularin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802773 GCST90242000 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetyl-D-glucosamine kinase levels (NAGK.3894.15.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 N-acetyl-D-glucosamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0008239 GCST90242001 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. N-acetylated-alpha-linked acidic dipeptidase 2 levels (NAALAD2.7986.98.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 n-acetylated-alpha-linked acidic dipeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801815 GCST90242002 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal-regulatory protein gamma levels (SIRPG.9241.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 signal-regulatory protein gamma measurement http://www.ebi.ac.uk/efo/EFO_0802071 GCST90242822 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal-transducing adaptor protein 1 levels (STAP1.12510.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 signal-transducing adaptor protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803075 GCST90242823 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine protease HTRA2, mitochondrial levels (HTRA2.3317.33.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine protease HTRA2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020723 GCST90242761 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine protease inhibitor Kazal-type 13 levels (SPINK13.10624.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine protease inhibitor Kazal-type 13 measurement http://www.ebi.ac.uk/efo/EFO_0803057 GCST90242762 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine protease inhibitor Kazal-type 2 levels (SPINK2.13405.61.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 serine protease inhibitor Kazal-type 2 measurement http://www.ebi.ac.uk/efo/EFO_0802054 GCST90242763 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine protease inhibitor Kazal-type 5 levels (SPINK5.8028.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine protease inhibitor Kazal-type 5 measurement http://www.ebi.ac.uk/efo/EFO_0803058 GCST90242764 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine protease inhibitor Kazal-type 6 levels (SPINK6.5731.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 serine protease inhibitor Kazal-type 6 measurement http://www.ebi.ac.uk/efo/EFO_0802055 GCST90242765 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine protease inhibitor Kazal-type 8 levels (SPINK8.7962.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine protease inhibitor Kazal-type 8 measurement http://www.ebi.ac.uk/efo/EFO_0803059 GCST90242766 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine protease inhibitor Kazal-type 9 levels (SPINK9.8042.88.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine protease inhibitor Kazal-type 9 measurement http://www.ebi.ac.uk/efo/EFO_0803060 GCST90242767 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine--tRNA ligase, mitochondrial levels (SARS2.12348.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine--tRNA ligase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0803061 GCST90242768 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine-rich single-pass membrane protein 1 levels (SSMEM1.8298.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serine-rich single-pass membrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802056 GCST90242769 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/arginine-rich splicing factor 6 levels (SRSF6.11573.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/arginine-rich splicing factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0803062 GCST90242770 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/arginine-rich splicing factor 7 levels (SRSF7.12987.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serine/arginine-rich splicing factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0802057 GCST90242771 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase 16 levels (STK16.3471.49.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 serine/threonine-protein kinase 16 measurement http://www.ebi.ac.uk/efo/EFO_0020724 GCST90242772 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase 17B levels (STK17B.5249.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serine/threonine-protein kinase 17B measurement http://www.ebi.ac.uk/efo/EFO_0008281 GCST90242773 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase BRSK2 levels (BRSK2.9790.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase BRSK2 measurement http://www.ebi.ac.uk/efo/EFO_0803063 GCST90242774 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase Chk1 levels (CHEK1.2853.68.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase Chk1 measurement http://www.ebi.ac.uk/efo/EFO_0021965 GCST90242775 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase DCLK3 levels (DCLK3.7826.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase DCLK3 measurement http://www.ebi.ac.uk/efo/EFO_0803064 GCST90242776 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase MRCK alpha levels (CDC42BPA.12706.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 serine/threonine-protein kinase MRCK alpha measurement http://www.ebi.ac.uk/efo/EFO_0802058 GCST90242777 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase MRCK beta levels (CDC42BPB.3629.60.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase MRCK beta measurement http://www.ebi.ac.uk/efo/EFO_0020727 GCST90242778 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase PAK 3 levels (PAK3.3387.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase PAK 3 measurement http://www.ebi.ac.uk/efo/EFO_0020728 GCST90242779 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase PAK 4 levels (PAK4.13719.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serine/threonine-protein kinase PAK 4 measurement http://www.ebi.ac.uk/efo/EFO_0802059 GCST90242780 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase PAK 7 levels (PAK7.3388.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase PAK 7 measurement http://www.ebi.ac.uk/efo/EFO_0020730 GCST90242781 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase pim-1 levels (PIM1.5359.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serine/threonine-protein kinase PIM-1 measurement http://www.ebi.ac.uk/efo/EFO_0020731 GCST90242782 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase PLK1 levels (PLK1.3394.81.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase PLK1 measurement http://www.ebi.ac.uk/efo/EFO_0020732 GCST90242783 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase receptor R3 levels (ACVRL1.2969.11.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase receptor R3 measurement http://www.ebi.ac.uk/efo/EFO_0020733 GCST90242784 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase TBK1 levels (TBK1.3400.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase TBK1 measurement http://www.ebi.ac.uk/efo/EFO_0020734 GCST90242785 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase ULK3 levels (ULK3.12437.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase ULK3 measurement http://www.ebi.ac.uk/efo/EFO_0803065 GCST90242786 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase VRK1 levels (VRK1.12553.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase VRK1 measurement http://www.ebi.ac.uk/efo/EFO_0803066 GCST90242787 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein kinase WNK3 levels (WNK3.5493.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein kinase WNK3 measurement http://www.ebi.ac.uk/efo/EFO_0021992 GCST90242788 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform levels (PPP2R1A.12621.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform measurement http://www.ebi.ac.uk/efo/EFO_0803067 GCST90242789 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit alpha levels (PPP2R3A.13665.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0802060 GCST90242790 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serotransferrin levels (TF.4162.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020735 GCST90242791 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serpin A12 levels (SERPINA12.6551.94.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 serpin A12 measurement http://www.ebi.ac.uk/efo/EFO_0802061 GCST90242792 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serpin A9 levels (SERPINA9.7266.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serpin A9 measurement http://www.ebi.ac.uk/efo/EFO_0802062 GCST90242793 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serpin I2 levels (SERPINI2.7117.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serpin I2 measurement http://www.ebi.ac.uk/efo/EFO_0803068 GCST90242794 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serum amyloid A-1 protein levels (SAA1.4336.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90242795 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serum amyloid P-component levels (APCS.2474.54.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 serum amyloid P-component measurement http://www.ebi.ac.uk/efo/EFO_0008283 GCST90242796 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Set1/Ash2 histone methyltransferase complex subunit ASH2 levels (ASH2L.12832.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 set1/Ash2 histone methyltransferase complex subunit ASH2 measurement http://www.ebi.ac.uk/efo/EFO_0803069 GCST90242797 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SH2 domain-containing protein 1A levels (SH2D1A.4567.82.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sh2 domain-containing protein 1a measurement http://www.ebi.ac.uk/efo/EFO_0020737 GCST90242798 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SH3 domain-binding protein 2 levels (SH3BP2.7769.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 SH3 domain-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802063 GCST90242799 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SHC-transforming protein 1 levels (SHC1.5272.55.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 shc-transforming protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020738 GCST90242800 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SHC-transforming protein 2 levels (SHC2.14074.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SHC-transforming protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803070 GCST90242801 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SHC-transforming protein 4 levels (SHC4.11692.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SHC-transforming protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803071 GCST90242802 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sia-alpha-2,3-Gal-beta-1,4-GlcNAc-R:alpha 2,8-sialyltransferase levels (ST8SIA3.6929.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sia-alpha-2,3-Gal-beta-1,4-GlcNAc-R:alpha 2,8-sialyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0803072 GCST90242803 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialate O-acetylesterase levels (SIAE.9263.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sialate O-acetylesterase measurement http://www.ebi.ac.uk/efo/EFO_0803073 GCST90242804 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 10 levels (SIGLEC10.6048.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 sialic acid-binding Ig-like lectin 10 measurement http://www.ebi.ac.uk/efo/EFO_0802064 GCST90242805 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 11 levels (SIGLEC11.8913.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 sialic acid-binding Ig-like lectin 11 measurement http://www.ebi.ac.uk/efo/EFO_0802065 GCST90242806 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 12 levels (SIGLEC12.8352.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 sialic acid-binding Ig-like lectin 12 measurement http://www.ebi.ac.uk/efo/EFO_0802066 GCST90242807 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 12 levels (SIGLEC12.10037.98.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sialic acid-binding Ig-like lectin 12 measurement http://www.ebi.ac.uk/efo/EFO_0802066 GCST90242808 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-crystallin D levels (CRYGD.12366.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gamma-crystallin D measurement http://www.ebi.ac.uk/efo/EFO_0802560 GCST90241232 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-enolase levels (ENO2.11083.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gamma-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021845 GCST90241233 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-enolase levels (ENO2.10339.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gamma-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021845 GCST90241234 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-glutamyl hydrolase levels (GGH.9370.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 gamma-glutamyl hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0801616 GCST90241235 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-interferon-inducible protein 16 levels (IFI16.12893.159.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 gamma-interferon-inducible protein 16 measurement http://www.ebi.ac.uk/efo/EFO_0801617 GCST90241236 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-interferon-inducible protein 16 levels (IFI16.13940.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gamma-interferon-inducible protein 16 measurement http://www.ebi.ac.uk/efo/EFO_0801617 GCST90241237 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gap junction alpha-1 protein levels (GJA1.9937.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gap junction alpha-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0801618 GCST90241238 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gap junction alpha-8 protein levels (GJA8.12711.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gap junction alpha-8 protein measurement http://www.ebi.ac.uk/efo/EFO_0802561 GCST90241239 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gap junction delta-2 protein levels (GJD2.11678.105.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gap junction delta-2 protein measurement http://www.ebi.ac.uk/efo/EFO_0802562 GCST90241240 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gastric triacylglycerol lipase levels (LIPF.9353.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gastric triacylglycerol lipase measurement http://www.ebi.ac.uk/efo/EFO_0802563 GCST90241241 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gastrin-releasing peptide levels (GRP.8339.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 gastrin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0022000 GCST90241242 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gastrin-releasing peptide levels (GRP.5897.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gastrin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0022000 GCST90241243 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gastrin-releasing peptide levels (GRP.8400.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gastrin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0022000 GCST90241244 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDH/6PGL endoplasmic bifunctional protein levels (H6PD.7161.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 GDH/6PGL endoplasmic bifunctional protein measurement http://www.ebi.ac.uk/efo/EFO_0801619 GCST90241245 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDNF family receptor alpha-1 levels (GFRA1.3314.74.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gdnf family receptor alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020400 GCST90241246 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDNF family receptor alpha-2 levels (GFRA2.2515.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 GDNF family receptor alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0008138 GCST90241247 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDNF family receptor alpha-3 levels (GFRA3.2505.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gdnf family receptor alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020401 GCST90241248 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDNF family receptor alpha-like levels (GFRAL.6920.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 GDNF family receptor alpha-like measurement http://www.ebi.ac.uk/efo/EFO_0801620 GCST90241249 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDP-fucose protein O-fucosyltransferase 1 levels (POFUT1.5634.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 GDP-fucose protein O-fucosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801621 GCST90241250 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDP-fucose protein O-fucosyltransferase 2 levels (POFUT2.6042.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 GDP-fucose protein O-fucosyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801622 GCST90241251 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal transducer and activator of transcription 1-alpha/beta levels (STAT1.10370.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 signal transducer and activator of transcription 1-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0021915 GCST90242817 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal transducer and activator of transcription 3 levels (STAT3.10346.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 signal transducer and activator of transcription 3 measurement http://www.ebi.ac.uk/efo/EFO_0021907 GCST90242818 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal transducer and activator of transcription 6 levels (STAT6.10372.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 signal transducer and activator of transcription 6 measurement http://www.ebi.ac.uk/efo/EFO_0021916 GCST90242819 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal-regulatory protein beta-1 levels (SIRPB1.6247.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 signal-regulatory protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0802069 GCST90242820 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal-regulatory protein beta-2 levels (SIRPB2.5669.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 signal-regulatory protein beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0802070 GCST90242821 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fructose-1,6-bisphosphatase isozyme 2 levels (FBP2.9867.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fructose-1,6-bisphosphatase isozyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0802556 GCST90241207 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fructose-2,6-bisphosphatase TIGAR levels (TIGAR.12476.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fructose-2,6-bisphosphatase TIGAR measurement http://www.ebi.ac.uk/efo/EFO_0801607 GCST90241208 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fructose-bisphosphate aldolase A levels (ALDOA.5864.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fructose-bisphosphate aldolase A measurement http://www.ebi.ac.uk/efo/EFO_0801608 GCST90241209 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fructose-bisphosphate aldolase C levels (ALDOC.9876.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fructose-bisphosphate aldolase C measurement http://www.ebi.ac.uk/efo/EFO_0802557 GCST90241210 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fumarylacetoacetase levels (FAH.11424.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fumarylacetoacetase measurement http://www.ebi.ac.uk/efo/EFO_0801609 GCST90241211 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Furin levels (FURIN.6276.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 furin measurement http://www.ebi.ac.uk/efo/EFO_0801610 GCST90241212 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. G-protein coupled receptor 26 levels (GPR26.13540.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 g-protein coupled receptor 26 measurement http://www.ebi.ac.uk/efo/EFO_0802558 GCST90241213 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. G0/G1 switch protein 2 levels (G0S2.8931.124.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 G0/G1 switch protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802559 GCST90241214 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. G2/mitotic-specific cyclin-B1 levels (CCNB1.5347.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 g2/mitotic-specific cyclin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020396 GCST90241215 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galactoside 3(4)-L-fucosyltransferase levels (FUT3.4548.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 galactoside 3(4)-L-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0021853 GCST90241216 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 levels (B3GAT3.6897.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801611 GCST90241217 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galanin peptides levels (GAL.13389.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 galanin peptides measurement http://www.ebi.ac.uk/efo/EFO_0010615 GCST90241218 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galanin-like peptide levels (GALP.9398.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 galanin-like peptide measurement http://www.ebi.ac.uk/efo/EFO_0801612 GCST90241219 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-1 levels (LGALS1.8046.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 galectin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020932 GCST90241220 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-10 levels (CLC.11094.104.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 galectin-10 measurement http://www.ebi.ac.uk/efo/EFO_0021918 GCST90241221 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-2 levels (LGALS2.3033.57.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 galectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020397 GCST90241222 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-4 levels (LGALS4.2982.82.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 galectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020398 GCST90241223 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-7 levels (LGALS7.9196.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 galectin-7 measurement http://www.ebi.ac.uk/efo/EFO_0022034 GCST90241224 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-7 levels (LGALS7.9400.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 galectin-7 measurement http://www.ebi.ac.uk/efo/EFO_0022034 GCST90241225 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-8 levels (LGALS8.4909.68.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 galectin-8 measurement http://www.ebi.ac.uk/efo/EFO_0020399 GCST90241226 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Galectin-9 levels (LGALS9.9197.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 galectin-9 measurement http://www.ebi.ac.uk/efo/EFO_0021863 GCST90241227 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-aminobutyric acid receptor-associated protein-like 1 levels (GABARAPL1.12661.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gamma-aminobutyric acid receptor-associated protein-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801613 GCST90241228 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-aminobutyric acid receptor-associated protein-like 2 levels (GABARAPL2.12494.99.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gamma-aminobutyric acid receptor-associated protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801614 GCST90241229 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-aminobutyric acid type B receptor subunit 2 levels (GABBR2.13948.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 gamma-aminobutyric acid type B receptor subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0801615 GCST90241230 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gamma-aminobutyric acid type B receptor subunit 2 levels (GABBR2.9930.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gamma-aminobutyric acid type B receptor subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0801615 GCST90241231 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Surfeit locus protein 1 levels (SURF1.8009.121.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 surfeit locus protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802105 GCST90242924 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sushi domain-containing protein 2 levels (SUSD2.10021.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 Sushi domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802106 GCST90242926 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 levels (SVEP1.11178.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 8 Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803113 GCST90242928 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 levels (SVEP1.11109.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803113 GCST90242929 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related levels (HMG20B.11551.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related measurement http://www.ebi.ac.uk/efo/EFO_0803114 GCST90242930 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Switch-associated protein 70 levels (SWAP70.13552.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 switch-associated protein 70 measurement http://www.ebi.ac.uk/efo/EFO_0802107 GCST90242931 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptic vesicle glycoprotein 2A levels (SV2A.12880.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptic vesicle glycoprotein 2A measurement http://www.ebi.ac.uk/efo/EFO_0803115 GCST90242932 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptosomal-associated protein 25 levels (SNAP25.13105.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 synaptosomal-associated protein 25 measurement http://www.ebi.ac.uk/efo/EFO_0021858 GCST90242933 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptosomal-associated protein 29 levels (SNAP29.12357.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptosomal-associated protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0803116 GCST90242934 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-17 levels (SYT17.9110.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptotagmin-17 measurement http://www.ebi.ac.uk/efo/EFO_0803117 GCST90242936 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-7 levels (SYT7.7121.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptotagmin-7 measurement http://www.ebi.ac.uk/efo/EFO_0803121 GCST90242940 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-8 levels (SYT8.7932.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptotagmin-8 measurement http://www.ebi.ac.uk/efo/EFO_0803122 GCST90242941 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-like protein 1 levels (SYTL1.12892.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 synaptotagmin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803123 GCST90242942 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Synaptotagmin-like protein 4 levels (SYTL4.11563.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 synaptotagmin-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802109 GCST90242943 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Syntaxin-18 levels (STX18.9037.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 syntaxin-18 measurement http://www.ebi.ac.uk/efo/EFO_0803124 GCST90242945 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Guanylyl cyclase-activating protein 1 levels (GUCA1A.10008.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 guanylyl cyclase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801663 GCST90241369 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Haloacid dehalogenase-like hydrolase domain-containing protein 2 levels (HDHD2.13472.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 haloacid dehalogenase-like hydrolase domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801664 GCST90241370 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tropomyosin alpha-3 chain levels (TPM3.12372.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tropomyosin alpha-3 chain measurement http://www.ebi.ac.uk/efo/EFO_0803196 GCST90243121 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tropomyosin beta chain levels (TPM2.4472.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tropomyosin beta chain measurement http://www.ebi.ac.uk/efo/EFO_0020787 GCST90243122 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Troponin I, cardiac muscle levels (TNNI3.5930.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 troponin i, cardiac muscle measurement http://www.ebi.ac.uk/efo/EFO_0020788 GCST90243123 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Troponin I, cardiac muscle levels (TNNI3.5441.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 troponin i, cardiac muscle measurement http://www.ebi.ac.uk/efo/EFO_0020788 GCST90243124 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trypsin-1 levels (PRSS1.3049.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 trypsin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020790 GCST90243125 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trypsin-2 levels (PRSS2.5034.79.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 trypsin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008305 GCST90243126 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trypsin-3 levels (PRSS3.3479.71.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 trypsin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020791 GCST90243127 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tryptase beta-2 levels (TPSB2.3403.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90243128 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tryptase gamma levels (TPSG1.14103.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tryptase gamma measurement http://www.ebi.ac.uk/efo/EFO_0020792 GCST90243129 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tuberoinfundibular peptide of 39 residues levels (PTH2.7257.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tuberoinfundibular peptide of 39 residues measurement http://www.ebi.ac.uk/efo/EFO_0802163 GCST90243130 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tubulin polymerization-promoting protein family member 2 levels (TPPP2.12800.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tubulin polymerization-promoting protein family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802164 GCST90243131 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tubulin--tyrosine ligase levels (TTL.13973.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tubulin--tyrosine ligase measurement http://www.ebi.ac.uk/efo/EFO_0802165 GCST90243132 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tubulin-specific chaperone A levels (TBCA.12501.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 tubulin-specific chaperone A measurement http://www.ebi.ac.uk/efo/EFO_0802166 GCST90243133 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tubulin-specific chaperone E levels (TBCE.11211.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tubulin-specific chaperone E measurement http://www.ebi.ac.uk/efo/EFO_0802167 GCST90243134 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tubulointerstitial nephritis antigen-like levels (TINAGL1.11192.168.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tubulointerstitial nephritis antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0803197 GCST90243135 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tuftelin levels (TUFT1.5690.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tuftelin measurement http://www.ebi.ac.uk/efo/EFO_0803198 GCST90243136 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tuftelin-interacting protein 11 levels (TFIP11.9043.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tuftelin-interacting protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0803199 GCST90243137 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor levels (TNF.5936.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90243138 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor alpha-induced protein 3 levels (TNFAIP3.14009.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor alpha-induced protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803200 GCST90243139 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 11 levels (TNFSF11.2917.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90243140 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 12 levels (TNFSF12.5939.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tumor necrosis factor ligand superfamily member 12 measurement http://www.ebi.ac.uk/efo/EFO_0010801 GCST90243141 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 13B levels (TNFSF13B.3059.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020793 GCST90243142 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 14 levels (TNFSF14.5355.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90243143 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 15 levels (TNFSF15.2968.61.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90243144 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 15 levels (TNFSF15.14057.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90243145 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 234 levels (TMEM234.8107.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 234 measurement http://www.ebi.ac.uk/efo/EFO_0803183 GCST90243096 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 237 levels (TMEM237.12856.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 237 measurement http://www.ebi.ac.uk/efo/EFO_0803184 GCST90243097 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 40 levels (TMEM40.12941.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 40 measurement http://www.ebi.ac.uk/efo/EFO_0803185 GCST90243098 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 41B levels (TMEM41B.10661.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 41B measurement http://www.ebi.ac.uk/efo/EFO_0803186 GCST90243099 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 52 levels (TMEM52.11186.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 52 measurement http://www.ebi.ac.uk/efo/EFO_0803187 GCST90243100 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 59-like levels (TMEM59L.9959.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 transmembrane protein 59-like measurement http://www.ebi.ac.uk/efo/EFO_0802157 GCST90243101 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 70, mitochondrial levels (TMEM70.8074.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 70, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0803188 GCST90243102 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 87B levels (TMEM87B.13485.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 transmembrane protein 87B measurement http://www.ebi.ac.uk/efo/EFO_0802158 GCST90243103 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 8B levels (TMEM8B.12742.160.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 8B measurement http://www.ebi.ac.uk/efo/EFO_0803189 GCST90243104 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 9 levels (TMEM9.9249.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0803190 GCST90243105 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein C16orf54 levels (C16orf54.12394.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein C16orf54 measurement http://www.ebi.ac.uk/efo/EFO_0803191 GCST90243106 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein PVRIG levels (PVRIG.6464.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein PVRIG measurement http://www.ebi.ac.uk/efo/EFO_0803192 GCST90243107 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trefoil factor 1 levels (TFF1.9185.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 trefoil factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021865 GCST90243108 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trefoil factor 2 levels (TFF2.9191.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 trefoil factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0021846 GCST90243109 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trefoil factor 3 levels (TFF3.4721.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90243110 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trefoil factor 3 levels (TFF3.8323.163.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90243111 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trem-like transcript 1 protein levels (TREML1.9329.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 trem-like transcript 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0803193 GCST90243112 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trem-like transcript 2 protein levels (TREML2.5736.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 trem-like transcript 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0802159 GCST90243113 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Trem-like transcript 4 protein levels (TREML4.11139.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 trem-like transcript 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0802160 GCST90243114 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Triggering receptor expressed on myeloid cells 1 levels (TREM1.9266.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 triggering receptor expressed on myeloid cells 1 measurement http://www.ebi.ac.uk/efo/EFO_0802161 GCST90243115 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Triosephosphate isomerase levels (TPI1.4309.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 triosephosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020785 GCST90243116 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. tRNA (guanine-N(7)-)-methyltransferase levels (METTL1.12514.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tRNA (guanine-N(7)-)-methyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802162 GCST90243117 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. tRNA pseudouridine synthase A, mitochondrial levels (PUS1.11201.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tRNA pseudouridine synthase A, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0803194 GCST90243118 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tropomodulin-1 levels (TMOD1.12595.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tropomodulin-1 measurement http://www.ebi.ac.uk/efo/EFO_0803195 GCST90243119 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tropomyosin alpha-1 chain levels (TPM1.5033.27.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tropomyosin alpha-1 chain measurement http://www.ebi.ac.uk/efo/EFO_0020786 GCST90243120 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 1B levels (TNFRSF1B.8368.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90243171 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 1B levels (TNFRSF1B.3152.57.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90243172 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 21 levels (TNFRSF21.5404.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 21 measurement http://www.ebi.ac.uk/efo/EFO_0020810 GCST90243173 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 21 levels (TNFRSF21.9259.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 21 measurement http://www.ebi.ac.uk/efo/EFO_0020810 GCST90243174 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 27 levels (EDA2R.3083.71.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 27 measurement http://www.ebi.ac.uk/efo/EFO_0020812 GCST90243175 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 3 levels (LTBR.2636.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tumor necrosis factor receptor superfamily member 3 measurement http://www.ebi.ac.uk/efo/EFO_0020813 GCST90243176 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 4 levels (TNFRSF4.3730.81.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020814 GCST90243177 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 6 levels (FAS.9459.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90243178 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17 receptor A levels (IL17RA.2992.59.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 interleukin-17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0801718 GCST90241597 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17 receptor B levels (IL17RB.5084.154.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0801719 GCST90241598 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17 receptor C levels (IL17RC.5468.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-17 receptor c measurement http://www.ebi.ac.uk/efo/EFO_0020494 GCST90241599 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17 receptor D levels (IL17RD.3376.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-17 receptor D measurement http://www.ebi.ac.uk/efo/EFO_0801720 GCST90241600 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17A levels (IL17A.9170.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90241601 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17A levels (IL17A.13718.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90241602 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17A levels (IL17A.3498.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90241603 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17C levels (IL17C.9255.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-17C measurement http://www.ebi.ac.uk/efo/EFO_0802656 GCST90241604 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17D levels (IL17D.4136.40.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-17D measurement http://www.ebi.ac.uk/efo/EFO_0021976 GCST90241605 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-17F levels (IL17F.2775.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-17F measurement http://www.ebi.ac.uk/efo/EFO_0021963 GCST90241606 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-18 receptor 1 levels (IL18R1.3446.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 interleukin-18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801721 GCST90241607 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-18 receptor 1 levels (IL18R1.14079.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801721 GCST90241608 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-18-binding protein levels (IL18BP.3073.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-18-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020495 GCST90241609 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-19 levels (IL19.3035.80.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-19 measurement http://www.ebi.ac.uk/efo/EFO_0801722 GCST90241610 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-2 levels (IL2.3070.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801723 GCST90241611 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-2 receptor subunit alpha levels (IL2RA.3151.6.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0010587 GCST90241612 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-2 receptor subunit beta levels (IL2RB.9343.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-2 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0802657 GCST90241613 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 18 levels (TNFSF18.2708.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020795 GCST90243146 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 4 levels (TNFSF4.14030.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020796 GCST90243147 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 4 levels (TNFSF4.2839.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020796 GCST90243148 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 6, soluble form levels (FASLG.3052.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tumor necrosis factor ligand superfamily member 6, soluble form measurement http://www.ebi.ac.uk/efo/EFO_0020797 GCST90243149 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 8 levels (TNFSF8.3421.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90243150 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor ligand superfamily member 9 levels (TNFSF9.2599.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor ligand superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0020798 GCST90243151 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 10A levels (TNFRSF10A.4832.75.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 10A measurement http://www.ebi.ac.uk/efo/EFO_0020799 GCST90243152 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 10B levels (TNFRSF10B.7693.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 10B measurement http://www.ebi.ac.uk/efo/EFO_0021993 GCST90243153 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 10D levels (TNFRSF10D.14121.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 10D measurement http://www.ebi.ac.uk/efo/EFO_0021942 GCST90243154 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 11A levels (TNFRSF11A.8316.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tumor necrosis factor receptor superfamily member 11A measurement http://www.ebi.ac.uk/efo/EFO_0020800 GCST90243155 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 11A levels (TNFRSF11A.5424.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 11A measurement http://www.ebi.ac.uk/efo/EFO_0020800 GCST90243156 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 11A levels (TNFRSF11A.8256.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 11A measurement http://www.ebi.ac.uk/efo/EFO_0020800 GCST90243157 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 11B levels (TNFRSF11B.2526.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 tumor necrosis factor receptor superfamily member 11B measurement http://www.ebi.ac.uk/efo/EFO_0020801 GCST90243158 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 11B levels (TNFRSF11B.8304.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 11B measurement http://www.ebi.ac.uk/efo/EFO_0020801 GCST90243159 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 12A levels (TNFRSF12A.5138.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 12A measurement http://www.ebi.ac.uk/efo/EFO_0020802 GCST90243160 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 13B levels (TNFRSF13B.2704.74.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020803 GCST90243161 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 14 levels (TNFRSF14.5352.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0020805 GCST90243162 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 16 levels (NGFR.8949.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 tumor necrosis factor receptor superfamily member 16 measurement http://www.ebi.ac.uk/efo/EFO_0802168 GCST90243163 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 16 levels (NGFR.8374.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 16 measurement http://www.ebi.ac.uk/efo/EFO_0802168 GCST90243164 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 17 levels (TNFRSF17.2665.26.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 17 measurement http://www.ebi.ac.uk/efo/EFO_0020806 GCST90243165 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 18 levels (TNFRSF18.5526.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020807 GCST90243166 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 19 levels (TNFRSF19.5131.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 19 measurement http://www.ebi.ac.uk/efo/EFO_0020808 GCST90243167 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 19L levels (RELT.5115.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90243168 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 19L levels (RELT.14112.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90243169 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Tumor necrosis factor receptor superfamily member 1A levels (TNFRSF1A.2654.19.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 tumor necrosis factor receptor superfamily member 1A measurement http://www.ebi.ac.uk/efo/EFO_0803201 GCST90243170 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; IFNβ-1b subcutaneous) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 2 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093352 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; IFNβ-1a subcutaneous and intramuscular) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093353 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; IFNβ-1a subcutaneous) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093354 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (antibody titre; all treatment preparations) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093355 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; IFNβ-1b subcutaneous) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 2 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093356 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; IFNβ-1a subcutaneous and intramuscular) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093357 Genome-wide genotyping array 2022-01-31 33143745 Andlauer TFM 2020-11-04 BMC Med www.ncbi.nlm.nih.gov/pubmed/33143745 Treatment- and population-specific genetic risk factors for anti-drug antibodies against interferon-beta: a GWAS. Neutralising antibody response to interferon beta therapy in multiple sclerosis (presence of antibodies; IFNβ-1a subcutaneous) up to 2,000 German and Swedish ancestry individuals up to 757 German and Swedish ancestry individuals Illumina [8550834] (imputed) 1 response to interferon-beta, anti-drug antibody measurement http://purl.obolibrary.org/obo/GO_0035456, http://www.ebi.ac.uk/efo/EFO_0010559 GCST90093358 Genome-wide genotyping array 2022-03-23 35047121 Gao Y 2021-12-01 World J Diabetes www.ncbi.nlm.nih.gov/pubmed/35047121 Genome-wide association study reveals novel loci for adult type 1 diabetes in a 5-year nested case-control study. Type 1 diabetes 381 Chinese ancestry cases, 377 Chinese ancestry controls 404 Chinese ancestry cases, 427 Chinese ancestry controls NR [920636] (imputed) 1 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90095483 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin carboxyl-terminal hydrolase 21 levels (USP21.12681.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ubiquitin carboxyl-terminal hydrolase 21 measurement http://www.ebi.ac.uk/efo/EFO_0802178 GCST90243229 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin carboxyl-terminal hydrolase 25 levels (USP25.9215.117.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 15 ubiquitin carboxyl-terminal hydrolase 25 measurement http://www.ebi.ac.uk/efo/EFO_0021881 GCST90243230 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin carboxyl-terminal hydrolase 8 levels (USP8.13450.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin carboxyl-terminal hydrolase 8 measurement http://www.ebi.ac.uk/efo/EFO_0802179 GCST90243231 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin domain-containing protein 2 levels (UBTD2.12875.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802180 GCST90243232 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin thioesterase OTUB2 levels (OTUB2.12493.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin thioesterase OTUB2 measurement http://www.ebi.ac.uk/efo/EFO_0803213 GCST90243233 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 B levels (UBE2B.9865.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-conjugating enzyme E2 B measurement http://www.ebi.ac.uk/efo/EFO_0803214 GCST90243234 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 D4 levels (UBE2D4.13475.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin-conjugating enzyme E2 D4 measurement http://www.ebi.ac.uk/efo/EFO_0802181 GCST90243235 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 G2 levels (UBE2G2.9199.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-conjugating enzyme E2 G2 measurement http://www.ebi.ac.uk/efo/EFO_0022035 GCST90243236 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 J1 levels (UBE2J1.6900.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-conjugating enzyme E2 J1 measurement http://www.ebi.ac.uk/efo/EFO_0803215 GCST90243237 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 J2 levels (UBE2J2.6601.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-conjugating enzyme E2 J2 measurement http://www.ebi.ac.uk/efo/EFO_0803216 GCST90243238 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 J2 levels (UBE2J2.8802.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-conjugating enzyme E2 J2 measurement http://www.ebi.ac.uk/efo/EFO_0803216 GCST90243239 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 L3 levels (UBE2L3.3874.8.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-conjugating enzyme E2 L3 measurement http://www.ebi.ac.uk/efo/EFO_0020840 GCST90243240 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 N levels (UBE2N.3905.62.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin-conjugating enzyme E2 N measurement http://www.ebi.ac.uk/efo/EFO_0020841 GCST90243241 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 T levels (UBE2T.12400.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-conjugating enzyme E2 T measurement http://www.ebi.ac.uk/efo/EFO_0803217 GCST90243242 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-conjugating enzyme E2 variant 1 levels (UBE2V1.11626.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin-conjugating enzyme E2 variant 1 measurement http://www.ebi.ac.uk/efo/EFO_0802182 GCST90243243 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-fold modifier 1 levels (UFM1.3836.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin-fold modifier 1 measurement http://www.ebi.ac.uk/efo/EFO_0020842 GCST90243244 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-fold modifier-conjugating enzyme 1 levels (UFC1.3405.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin-fold modifier-conjugating enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020843 GCST90243245 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-like modifier-activating enzyme ATG7 levels (ATG7.12627.97.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-like modifier-activating enzyme ATG7 measurement http://www.ebi.ac.uk/efo/EFO_0803218 GCST90243246 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-like protein 4A levels (UBL4A.11490.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin-like protein 4A measurement http://www.ebi.ac.uk/efo/EFO_0802183 GCST90243247 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-like protein ISG15 levels (ISG15.14151.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ubiquitin-like protein ISG15 measurement http://www.ebi.ac.uk/efo/EFO_0021875 GCST90243248 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin-like protein ISG15 levels (ISG15.14148.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ubiquitin-like protein ISG15 measurement http://www.ebi.ac.uk/efo/EFO_0021875 GCST90243249 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ubiquitin+1, truncated mutation for UbB levels (RPS27A.2846.24.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ubiquitin+1, truncated mutation for UBB measurement http://www.ebi.ac.uk/efo/EFO_0020844 GCST90243250 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UBX domain-containing protein 4 levels (UBXN4.9970.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UBX domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803219 GCST90243251 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UBX domain-containing protein 4 levels (UBXN4.9997.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UBX domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803219 GCST90243252 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 levels (B3GNT6.7082.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0803220 GCST90243253 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C6orf226 levels (C6orf226.8078.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 uncharacterized protein C6orf226 measurement http://www.ebi.ac.uk/efo/EFO_0802194 GCST90243279 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C7orf69 levels (C7orf69.9544.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein C7orf69 measurement http://www.ebi.ac.uk/efo/EFO_0802195 GCST90243280 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein KIAA0040 levels (KIAA0040.14603.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein KIAA0040 measurement http://www.ebi.ac.uk/efo/EFO_0802196 GCST90243281 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein KIAA1467 levels (KIAA1467.7892.132.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein KIAA1467 measurement http://www.ebi.ac.uk/efo/EFO_0803232 GCST90243282 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein KIAA2013 levels (KIAA2013.6538.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein KIAA2013 measurement http://www.ebi.ac.uk/efo/EFO_0802197 GCST90243283 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Unconventional myosin-VI levels (MYO6.9894.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 unconventional myosin-VI measurement http://www.ebi.ac.uk/efo/EFO_0803233 GCST90243284 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Unique cartilage matrix-associated protein levels (UCMA.10977.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 unique cartilage matrix-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0802198 GCST90243285 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0258 protein KIAA1024 levels (KIAA1024.9075.121.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UPF0258 protein KIAA1024 measurement http://www.ebi.ac.uk/efo/EFO_0803234 GCST90243286 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0454 protein C12orf49 levels (C12orf49.9387.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 UPF0454 protein C12orf49 measurement http://www.ebi.ac.uk/efo/EFO_0802199 GCST90243287 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0488 protein C8orf33 levels (C8orf33.9613.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 UPF0488 protein C8orf33 measurement http://www.ebi.ac.uk/efo/EFO_0802200 GCST90243288 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0577 protein KIAA1324 levels (KIAA1324.10637.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UPF0577 protein KIAA1324 measurement http://www.ebi.ac.uk/efo/EFO_0803235 GCST90243289 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0577 protein KIAA1324 levels (KIAA1324.9097.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UPF0577 protein KIAA1324 measurement http://www.ebi.ac.uk/efo/EFO_0803235 GCST90243290 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0577 protein KIAA1324-like levels (KIAA1324L.8363.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 UPF0577 protein KIAA1324-like measurement http://www.ebi.ac.uk/efo/EFO_0802201 GCST90243291 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0696 protein C11orf68 levels (C11orf68.8307.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 UPF0696 protein C11orf68 measurement http://www.ebi.ac.uk/efo/EFO_0802202 GCST90243292 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UPF0729 protein C18orf32 levels (C18orf32.8236.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UPF0729 protein C18orf32 measurement http://www.ebi.ac.uk/efo/EFO_0803236 GCST90243293 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Urea transporter 1 levels (SLC14A1.13430.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 urea transporter 1 measurement http://www.ebi.ac.uk/efo/EFO_0803237 GCST90243294 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kit ligand levels (KITLG.9377.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kit ligand measurement http://www.ebi.ac.uk/efo/EFO_0010612 GCST90241714 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kremen protein 1 levels (KREMEN1.6512.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kremen protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801749 GCST90241715 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kremen protein 2 levels (KREMEN2.3202.28.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 kremen protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020523 GCST90241716 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kunitz-type protease inhibitor 1 levels (SPINT1.2828.82.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Kunitz-type protease inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008199 GCST90241717 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kunitz-type protease inhibitor 2 levels (SPINT2.2843.13.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Kunitz-type protease inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008200 GCST90241718 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kunitz-type protease inhibitor 3 levels (SPINT3.7926.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kunitz-type protease inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0801750 GCST90241719 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kv channel-interacting protein 1 levels (KCNIP1.13650.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kv channel-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801751 GCST90241720 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kynureninase levels (KYNU.4559.64.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 kynureninase measurement http://www.ebi.ac.uk/efo/EFO_0008201 GCST90241721 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Kynurenine--oxoglutarate transaminase 3 levels (CCBL2.12682.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 kynurenine--oxoglutarate transaminase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801752 GCST90241722 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. L-lactate dehydrogenase B chain levels (LDHB.3890.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 L-lactate dehydrogenase B chain measurement http://www.ebi.ac.uk/efo/EFO_0020524 GCST90241723 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. L-lactate dehydrogenase C chain levels (LDHC.9828.86.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 l-lactate dehydrogenase C chain measurement http://www.ebi.ac.uk/efo/EFO_0802680 GCST90241724 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. L-Selectin levels (SELL.4831.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90241725 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactadherin levels (MFGE8.4455.89.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lactadherin measurement http://www.ebi.ac.uk/efo/EFO_0008203 GCST90241726 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactase-like protein levels (LCTL.10890.135.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lactase-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802681 GCST90241727 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactase-phlorizin hydrolase levels (LCT.9017.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 lactase-phlorizin hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0801753 GCST90241728 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactoferrin levels (LTF.2795.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lactoferrin measurement http://www.ebi.ac.uk/efo/EFO_0802682 GCST90241729 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactoperoxidase levels (LPO.4801.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 lactoperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0020525 GCST90241730 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactosylceramide 4-alpha-galactosyltransferase levels (A4GALT.8759.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lactosylceramide 4-alpha-galactosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802683 GCST90241731 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactotransferrin levels (LTF.2780.35.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 lactotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020526 GCST90241732 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lactoylglutathione lyase levels (GLO1.9883.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lactoylglutathione lyase measurement http://www.ebi.ac.uk/efo/EFO_0802684 GCST90241733 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ladinin-1 levels (LAD1.6407.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ladinin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802685 GCST90241734 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lamin-B1 levels (LMNB1.3889.64.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lamin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020527 GCST90241735 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lamina-associated polypeptide 2, isoforms beta/gamma levels (TMPO.8265.225.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lamina-associated polypeptide 2, isoforms beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0801754 GCST90241736 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Laminin levels (LAMA1.LAMB1.LAMC1.2728.62.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 laminin measurement http://www.ebi.ac.uk/efo/EFO_0020528 GCST90241737 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Laminin subunit alpha-4 levels (LAMA4.6577.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 laminin subunit alpha-4 measurement http://www.ebi.ac.uk/efo/EFO_0801755 GCST90241738 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Laminin subunit gamma-2 levels (LAMC2.9580.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 laminin subunit gamma-2 measurement http://www.ebi.ac.uk/efo/EFO_0801756 GCST90241739 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Latent-transforming growth factor beta-binding protein 4 levels (LTBP4.13133.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 latent-transforming growth factor beta-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021940 GCST90241740 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Layilin levels (LAYN.2635.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 layilin measurement http://www.ebi.ac.uk/efo/EFO_0020529 GCST90241741 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. LDLR chaperone MESD levels (MESDC2.5594.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 LDLR chaperone MESD measurement http://www.ebi.ac.uk/efo/EFO_0802686 GCST90241742 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Legumain levels (LGMN.3622.33.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 legumain measurement http://www.ebi.ac.uk/efo/EFO_0020530 GCST90241743 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leiomodin-1 levels (LMOD1.12504.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leiomodin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802687 GCST90241744 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. LEM domain-containing protein 1 levels (LEMD1.8040.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 LEM domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801757 GCST90241745 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leptin levels (LEP.2575.5.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90241746 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leptin levels (LEP.8484.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90241747 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leptin levels (LEP.8484.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90241748 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leptin receptor levels (LEPR.5400.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90241749 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leptin receptor levels (LEPR.9566.103.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90241750 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine carboxyl methyltransferase 1 levels (LCMT1.4237.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine carboxyl methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008207 GCST90241751 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich PPR motif-containing protein, mitochondrial levels (LRPPRC.9046.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 leucine-rich PPR motif-containing protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801758 GCST90241752 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and calponin homology domain-containing protein 4 levels (LRCH4.11252.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat and calponin homology domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802688 GCST90241753 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and calponin homology domain-containing protein 4 levels (LRCH4.8984.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat and calponin homology domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802688 GCST90241754 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and fibronectin type III domain-containing protein 1 levels (LRFN1.7910.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat and fibronectin type III domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802689 GCST90241755 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and fibronectin type-III domain-containing protein 2 levels (LRFN2.7200.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat and fibronectin type-III domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802690 GCST90241756 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1 levels (LINGO1.6620.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802691 GCST90241757 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 levels (LINGO3.10827.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802692 GCST90241758 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and transmembrane domain-containing protein 1 levels (LRTM1.9368.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat and transmembrane domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802693 GCST90241759 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat and transmembrane domain-containing protein 2 levels (LRTM2.8906.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 leucine-rich repeat and transmembrane domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801759 GCST90241760 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat LGI family member 3 levels (LGI3.8003.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat LGI family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802694 GCST90241761 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat neuronal protein 1 levels (LRRN1.11293.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 leucine-rich repeat neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801760 GCST90241762 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat neuronal protein 1 levels (LRRN1.11586.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801760 GCST90241763 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat neuronal protein 3 levels (LRRN3.10471.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat neuronal protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802695 GCST90241764 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat serine/threonine-protein kinase 2 levels (LRRK2.10990.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 leucine-rich repeat serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0021876 GCST90241765 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane neuronal protein 1 levels (LRRTM1.4452.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat transmembrane neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020531 GCST90241766 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane neuronal protein 2 levels (LRRTM2.6904.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat transmembrane neuronal protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802696 GCST90241767 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane neuronal protein 4 levels (LRRTM4.6572.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat transmembrane neuronal protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802697 GCST90241768 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane neuronal protein 4 levels (LRRTM4.8646.61.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat transmembrane neuronal protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802697 GCST90241769 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane protein FLRT1 levels (FLRT1.4547.59.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat transmembrane protein FLRT1 measurement http://www.ebi.ac.uk/efo/EFO_0020533 GCST90241770 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane protein FLRT1 levels (FLRT1.13739.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat transmembrane protein FLRT1 measurement http://www.ebi.ac.uk/efo/EFO_0020533 GCST90241771 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane protein FLRT2 levels (FLRT2.13122.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 leucine-rich repeat transmembrane protein FLRT2 measurement http://www.ebi.ac.uk/efo/EFO_0021860 GCST90241772 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 levels (B3GNT8.9297.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 measurement http://www.ebi.ac.uk/efo/EFO_0802184 GCST90243254 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UDP-glucuronic acid decarboxylase 1 levels (UXS1.8258.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UDP-glucuronic acid decarboxylase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803221 GCST90243255 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UDP-glucuronosyltransferase 1-6 levels (UGT1A6.7891.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 UDP-glucuronosyltransferase 1-6 measurement http://www.ebi.ac.uk/efo/EFO_0802185 GCST90243256 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UDP-glucuronosyltransferase 1-8 levels (UGT1A8.8899.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UDP-glucuronosyltransferase 1-8 measurement http://www.ebi.ac.uk/efo/EFO_0803222 GCST90243257 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UDP-glucuronosyltransferase 2A1 levels (UGT2A1.8907.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 UDP-glucuronosyltransferase 2A1 measurement http://www.ebi.ac.uk/efo/EFO_0802186 GCST90243258 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UDP-N-acetylhexosamine pyrophosphorylase levels (UAP1.13580.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 UDP-N-acetylhexosamine pyrophosphorylase measurement http://www.ebi.ac.uk/efo/EFO_0802187 GCST90243259 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UMP-CMP kinase levels (CMPK1.4786.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UMP-CMP kinase measurement http://www.ebi.ac.uk/efo/EFO_0008313 GCST90243260 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UMP-CMP kinase levels (CMPK1.8312.139.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UMP-CMP kinase measurement http://www.ebi.ac.uk/efo/EFO_0008313 GCST90243261 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized family 31 glucosidase KIAA1161 levels (KIAA1161.8068.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized family 31 glucosidase KIAA1161 measurement http://www.ebi.ac.uk/efo/EFO_0802188 GCST90243262 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized family 31 glucosidase KIAA1161 levels (KIAA1161.8093.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized family 31 glucosidase KIAA1161 measurement http://www.ebi.ac.uk/efo/EFO_0802188 GCST90243263 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C10orf35 levels (C10orf35.8220.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein C10orf35 measurement http://www.ebi.ac.uk/efo/EFO_0802189 GCST90243264 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C14orf93 levels (C14orf93.6439.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein C14orf93 measurement http://www.ebi.ac.uk/efo/EFO_0802190 GCST90243265 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C17orf67 levels (C17orf67.9070.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C17orf67 measurement http://www.ebi.ac.uk/efo/EFO_0803223 GCST90243266 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C17orf78 levels (C17orf78.8545.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein C17orf78 measurement http://www.ebi.ac.uk/efo/EFO_0802191 GCST90243267 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C17orf78 levels (C17orf78.6571.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C17orf78 measurement http://www.ebi.ac.uk/efo/EFO_0802191 GCST90243268 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C17orf89 levels (C17orf89.9030.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C17orf89 measurement http://www.ebi.ac.uk/efo/EFO_0803224 GCST90243269 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C19orf18 levels (C19orf18.9445.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C19orf18 measurement http://www.ebi.ac.uk/efo/EFO_0803225 GCST90243270 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C1orf115 levels (C1orf115.8366.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C1orf115 measurement http://www.ebi.ac.uk/efo/EFO_0803226 GCST90243271 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C1orf185 levels (C1orf185.10667.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C1orf185 measurement http://www.ebi.ac.uk/efo/EFO_0803227 GCST90243272 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C1orf198 levels (C1orf198.8035.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C1orf198 measurement http://www.ebi.ac.uk/efo/EFO_0803228 GCST90243273 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C1orf226 levels (C1orf226.7989.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C1orf226 measurement http://www.ebi.ac.uk/efo/EFO_0803229 GCST90243274 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C22orf15 levels (C22orf15.7073.69.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C22orf15 measurement http://www.ebi.ac.uk/efo/EFO_0803230 GCST90243275 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C2orf66 levels (C2orf66.5677.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein C2orf66 measurement http://www.ebi.ac.uk/efo/EFO_0802192 GCST90243276 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C2orf82 levels (C2orf82.9439.454.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uncharacterized protein C2orf82 measurement http://www.ebi.ac.uk/efo/EFO_0803231 GCST90243277 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uncharacterized protein C3orf18 levels (C3orf18.6994.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uncharacterized protein C3orf18 measurement http://www.ebi.ac.uk/efo/EFO_0802193 GCST90243278 Genome-wide genotyping array 2021-12-07 34601942 van Zuydam NR 2021-10-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34601942 Genome-Wide Association Study of Peripheral Artery Disease. Peripheral artery disease in ever smokers 7,404 Finnish ancestry cases, 205,693 Finnish ancestry controls, 7,404 non-Scandinavian ancestry cases, 205,693 non-Scandinavian ancestry controls, 7,404 British ancestry cases, 205,693 British ancestry controls NA Affymetrix, Illumina [NR] (imputed) 6 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90061372 Genome-wide genotyping array 2021-12-07 34601942 van Zuydam NR 2021-10-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34601942 Genome-Wide Association Study of Peripheral Artery Disease. Peripheral artery disease in non smokers 2,414 Finnish ancestry cases, 239,806 Finnish ancestry controls, 2,414 non-Scandinavian ancestry cases, 239,806 non-Scandinavian ancestry controls, 2,414 British ancestry cases, 239,806 British ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90061373 Genome-wide genotyping array 2021-12-07 34601942 van Zuydam NR 2021-10-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34601942 Genome-Wide Association Study of Peripheral Artery Disease. Peripheral artery disease in diabetes 3,846 Finnish ancestry cases, 28,881 Finnish ancestry controls, 3,846 non-Scandinavian ancestry cases, 28,881 non-Scandinavian ancestry controls, 3,846 British ancestry cases, 28,881 British ancestry controls NA Affymetrix, Illumina [NR] (imputed) 1 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90061374 Genome-wide genotyping array 2021-12-07 34601942 van Zuydam NR 2021-10-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34601942 Genome-Wide Association Study of Peripheral Artery Disease. Peripheral artery disease in non diabetes 6,732 Finnish ancestry cases, 416,855 Finnish ancestry controls, 6,732 non-Scandinavian ancestry cases, 416,855 non-Scandinavian ancestry controls, 6,732 British ancestry cases, 416,855 British ancestry controls NA Illumina [NR] (imputed) 7 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90061375 Genome-wide genotyping array 2021-12-07 34601942 van Zuydam NR 2021-10-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34601942 Genome-Wide Association Study of Peripheral Artery Disease. Peripheral artery disease x diabetes status interaction 10,576 European ancestry cases, 445,736 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 1 diabetes mellitus, peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0000400, http://www.ebi.ac.uk/efo/EFO_0004265 GCST90061376 Genome-wide genotyping array 2021-12-07 34601942 van Zuydam NR 2021-10-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34601942 Genome-Wide Association Study of Peripheral Artery Disease. Peripheral artery disease x smoking status interaction 9,818 European ancestry cases, 445,499 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 smoking status measurement, peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004265 GCST90061378 Genome-wide genotyping array 2022-01-05 34670813 Horimoto A 2021-10-20 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/34670813 Genome-Wide Admixture Mapping of Estimated Glomerular Filtration Rate and Chronic Kidney Disease Identify European and African Ancestry-of-Origin Loci in Hispanic and Latino Individuals in the United States. Estimated glomerular filtration rate 12,601 Hispanic/Latino individuals NA Illumina [NR] (imputed) 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90091242 Genome-wide genotyping array 2022-01-05 34670813 Horimoto A 2021-10-20 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/34670813 Genome-Wide Admixture Mapping of Estimated Glomerular Filtration Rate and Chronic Kidney Disease Identify European and African Ancestry-of-Origin Loci in Hispanic and Latino Individuals in the United States. Chronic kidney disease 12,601 Hispanic/Latino individuals NA Illumina [NR] (imputed) 2 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90091243 Genome-wide genotyping array 2021-12-07 34601942 van Zuydam NR 2021-10-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34601942 Genome-Wide Association Study of Peripheral Artery Disease. Peripheral artery disease 12,086 European ancestry cases, 449,548 European ancestry controls 31,307 cases, 211,753 controls, 3,164 East Asian ancestry cases, 20,134 East Asian ancestry controls Affymetrix, Illumina [NR] (imputed) 19 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90061371 Genome-wide genotyping array 2022-02-08 35074870 Chia R 2022-02-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35074870 Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study. Myasthenia gravis 1,873 European ancestry cases, 36,370 European ancestry controls 7,412 European ancestry individuals Illumina [24006246] (imputed) 7 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST90093061 Genome-wide genotyping array 2022-02-08 35074870 Chia R 2022-02-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35074870 Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study. Early-onset myasthenia gravis 595 European ancestry cases, 2,718 European ancestry controls NA Illumina [24006246] (imputed) 2 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST90093465 Genome-wide genotyping array 2022-02-08 35074870 Chia R 2022-02-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35074870 Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study. Late-onset myasthenia gravis 1,278 European ancestry cases, 33,652 European ancestry controls 308 European ancestry cases, 7,056 European ancestry controls Illumina [24006246] (imputed) 3 late-onset myasthenia gravis http://www.ebi.ac.uk/efo/EFO_1001490 GCST90093466 Genome-wide genotyping array 2022-02-11 34339498 Skjeflo EW 2021-08-02 Blood www.ncbi.nlm.nih.gov/pubmed/34339498 Elevated plasma concentration of complement factor C5 is associated with risk of future venous thromboembolism. Complement C5 levels 709 European ancestry individuals NA NR [1033970] (imputed) 0 complement C5 measurement http://www.ebi.ac.uk/efo/EFO_0020278 GCST90094399 Exome-wide sequencing 2022-02-01 33758299 Dhindsa RS 2021-03-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33758299 Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis. Idiopathic pulmonary fibrosis 752 European ancestry cases, 119,055 European ancestry controls 1,028 Finnish ancestry cases, 196,986 Finnish ancestry controls NR [564159] 16 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST90093310 Genome-wide sequencing, Exome-wide sequencing 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatocyte growth factor levels (HGF.2681.23.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90241397 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatocyte growth factor receptor levels (MET.2837.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 hepatocyte growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0008153 GCST90241398 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatocyte growth factor-regulated tyrosine kinase substrate levels (HGS.13644.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hepatocyte growth factor-regulated tyrosine kinase substrate measurement http://www.ebi.ac.uk/efo/EFO_0802595 GCST90241399 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepatocyte nuclear factor 1-alpha levels (HNF1A.11193.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hepatocyte nuclear factor 1-alpha measurement http://www.ebi.ac.uk/efo/EFO_0802596 GCST90241400 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hepcidin levels (HAMP.3504.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hepcidin measurement http://www.ebi.ac.uk/efo/EFO_0020440 GCST90241403 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Hephaestin-like protein 1 levels (HEPHL1.6354.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 hephaestin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802597 GCST90241404 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. HERV-H LTR-associating protein 2 levels (HHLA2.14132.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 HERV-H LTR-associating protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021948 GCST90241405 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoprotein A/B levels (HNRNPAB.4450.26.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 heterogeneous nuclear ribonucleoprotein a/b measurement http://www.ebi.ac.uk/efo/EFO_0020441 GCST90241406 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoprotein D-like levels (HNRNPDL.10852.114.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 heterogeneous nuclear ribonucleoprotein D-like measurement http://www.ebi.ac.uk/efo/EFO_0801673 GCST90241408 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoprotein K levels (HNRNPK.4994.178.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 heterogeneous nuclear ribonucleoprotein k measurement http://www.ebi.ac.uk/efo/EFO_0020442 GCST90241409 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoprotein Q levels (SYNCRIP.4224.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 heterogeneous nuclear ribonucleoprotein q measurement http://www.ebi.ac.uk/efo/EFO_0020443 GCST90241411 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Heterogeneous nuclear ribonucleoproteins C1/C2 levels (HNRNPC.11429.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 heterogeneous nuclear ribonucleoproteins C1/C2 measurement http://www.ebi.ac.uk/efo/EFO_0801675 GCST90241413 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon gamma receptor 2 levels (IFNGR2.9180.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90241556 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon lambda receptor 1 levels (IFNLR1.7192.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon lambda receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802646 GCST90241559 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon lambda-1 levels (IFNL1.13734.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon lambda-1 measurement http://www.ebi.ac.uk/efo/EFO_0020485 GCST90241561 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon regulatory factor 2 levels (IRF2.12801.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interferon regulatory factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0801709 GCST90241566 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon regulatory factor 6 levels (IRF6.9999.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon regulatory factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0802649 GCST90241568 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon regulatory factor 9 levels (IRF9.12439.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon regulatory factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0802650 GCST90241569 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon-induced protein with tetratricopeptide repeats 2 levels (IFIT2.9853.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon-induced protein with tetratricopeptide repeats 2 measurement http://www.ebi.ac.uk/efo/EFO_0802651 GCST90241570 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon-induced protein with tetratricopeptide repeats 3 levels (IFIT3.13642.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interferon-induced protein with tetratricopeptide repeats 3 measurement http://www.ebi.ac.uk/efo/EFO_0801710 GCST90241571 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin enhancer-binding factor 3 levels (ILF3.12759.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin enhancer-binding factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802652 GCST90241572 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 alpha levels (IL1A.4851.25.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST90241573 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 beta levels (IL1B.3037.62.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST90241574 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 Receptor accessory protein levels (IL1RAP.2630.12.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 interleukin-1 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0801711 GCST90241575 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 receptor type 2 levels (IL1R2.5666.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90241580 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 receptor-like 1 levels (IL1RL1.4234.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 interleukin-1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801713 GCST90241581 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 receptor-like 2 levels (IL1RL2.2994.71.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801714 GCST90241582 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-10 levels (IL10.2773.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90241583 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-10 receptor subunit beta levels (IL10RB.2631.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-10 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020489 GCST90241584 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-11 levels (IL11.4493.92.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-11 measurement http://www.ebi.ac.uk/efo/EFO_0020490 GCST90241585 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-11 receptor subunit alpha levels (IL11RA.3814.63.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-11 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020491 GCST90241586 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-12 levels (IL12A.IL12B.10367.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-12 measurement http://www.ebi.ac.uk/efo/EFO_0802654 GCST90241587 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-12 levels (IL12A.IL12B.10367.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-12 measurement http://www.ebi.ac.uk/efo/EFO_0802654 GCST90241588 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-12 levels (IL12A.IL12B.2455.17.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-12 measurement http://www.ebi.ac.uk/efo/EFO_0802654 GCST90241589 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-12 receptor subunit beta-1 levels (IL12RB1.2632.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0801715 GCST90241590 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-12 receptor subunit beta-2 levels (IL12RB2.3815.14.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-12 receptor subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020492 GCST90241591 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-13 levels (IL13.3072.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-13 measurement http://www.ebi.ac.uk/efo/EFO_0802655 GCST90241592 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-13 receptor subunit alpha-1 levels (IL13RA1.2633.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-13 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020493 GCST90241593 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-15 receptor subunit alpha levels (IL15RA.14054.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 interleukin-15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801716 GCST90241594 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-15 receptor subunit alpha levels (IL15RA.3445.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801716 GCST90241595 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-16 levels (IL16.2774.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 interleukin-16 measurement http://www.ebi.ac.uk/efo/EFO_0801717 GCST90241596 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transforming protein RhoA levels (RHOA.9855.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transforming protein RhoA measurement http://www.ebi.ac.uk/efo/EFO_0802144 GCST90243063 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transgelin levels (TAGLN.9756.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transgelin measurement http://www.ebi.ac.uk/efo/EFO_0803171 GCST90243064 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transketolase levels (TKT.4306.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transketolase measurement http://www.ebi.ac.uk/efo/EFO_0020783 GCST90243065 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Translation initiation factor eIF-2B subunit alpha levels (EIF2B1.10080.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 translation initiation factor eIF-2B subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0802145 GCST90243066 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Translationally-controlled tumor protein levels (TPT1.3872.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 translationally-controlled tumor protein measurement http://www.ebi.ac.uk/efo/EFO_0020784 GCST90243067 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Translin levels (TSN.12477.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 translin measurement http://www.ebi.ac.uk/efo/EFO_0803172 GCST90243068 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Translocon-associated protein subunit alpha levels (SSR1.8106.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 translocon-associated protein subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0803173 GCST90243069 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane and coiled-coil domain-containing protein 5A levels (TMCO5A.6907.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane and coiled-coil domain-containing protein 5A measurement http://www.ebi.ac.uk/efo/EFO_0803174 GCST90243070 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane and ubiquitin-like domain-containing protein 2 levels (TMUB2.9226.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane and ubiquitin-like domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803175 GCST90243071 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane emp24 domain-containing protein 10 levels (TMED10.6506.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 transmembrane emp24 domain-containing protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0802146 GCST90243072 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane emp24 domain-containing protein 2 levels (TMED2.10761.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane emp24 domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803176 GCST90243073 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane emp24 domain-containing protein 4 levels (TMED4.9319.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane emp24 domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803177 GCST90243074 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane gamma-carboxyglutamic acid protein 1 levels (PRRG1.9008.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transmembrane gamma-carboxyglutamic acid protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802147 GCST90243075 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane gamma-carboxyglutamic acid protein 1 levels (PRRG1.8306.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane gamma-carboxyglutamic acid protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802147 GCST90243076 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane gamma-carboxyglutamic acid protein 4 levels (PRRG4.9579.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane gamma-carboxyglutamic acid protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803178 GCST90243077 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane glycoprotein NMB levels (GPNMB.8606.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 8 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90243078 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane glycoprotein NMB levels (GPNMB.5080.131.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90243079 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane glycoprotein NMB levels (GPNMB.8240.207.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90243080 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane glycoprotein NMB levels (GPNMB.8289.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90243081 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane inner ear expressed protein levels (TMIE.7992.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 transmembrane inner ear expressed protein measurement http://www.ebi.ac.uk/efo/EFO_0802148 GCST90243082 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protease serine 11A levels (TMPRSS11A.7231.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protease serine 11A measurement http://www.ebi.ac.uk/efo/EFO_0803179 GCST90243083 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protease serine 11B levels (TMPRSS11B.10895.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protease serine 11B measurement http://www.ebi.ac.uk/efo/EFO_0803180 GCST90243084 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protease serine 11D levels (TMPRSS11D.6547.83.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transmembrane protease serine 11D measurement http://www.ebi.ac.uk/efo/EFO_0802149 GCST90243085 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protease serine 5 levels (TMPRSS5.8002.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protease serine 5 measurement http://www.ebi.ac.uk/efo/EFO_0803181 GCST90243086 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 119 levels (TMEM119.11110.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 119 measurement http://www.ebi.ac.uk/efo/EFO_0803182 GCST90243087 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 132A levels (TMEM132A.7871.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 transmembrane protein 132A measurement http://www.ebi.ac.uk/efo/EFO_0802150 GCST90243088 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 132B levels (TMEM132B.8890.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transmembrane protein 132B measurement http://www.ebi.ac.uk/efo/EFO_0802151 GCST90243089 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 132C levels (TMEM132C.7173.141.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 transmembrane protein 132C measurement http://www.ebi.ac.uk/efo/EFO_0802152 GCST90243090 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 132C levels (TMEM132C.11128.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 transmembrane protein 132C measurement http://www.ebi.ac.uk/efo/EFO_0802152 GCST90243091 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 132D levels (TMEM132D.13416.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transmembrane protein 132D measurement http://www.ebi.ac.uk/efo/EFO_0802153 GCST90243092 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 190 levels (TMEM190.10442.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transmembrane protein 190 measurement http://www.ebi.ac.uk/efo/EFO_0802154 GCST90243093 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 2 levels (TMEM2.8992.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 transmembrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802155 GCST90243094 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Transmembrane protein 230 levels (TMEM230.11542.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 transmembrane protein 230 measurement http://www.ebi.ac.uk/efo/EFO_0802156 GCST90243095 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integrin alpha-5 levels (ITGA5.6932.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integrin alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802637 GCST90241530 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integrin alpha-I: beta-1 complex levels (ITGA1.ITGB1.3503.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 integrin alpha-I: beta-1 complex measurement http://www.ebi.ac.uk/efo/EFO_0008162 GCST90241531 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integrin alpha-L levels (ITGAL.11617.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integrin alpha-L measurement http://www.ebi.ac.uk/efo/EFO_0802638 GCST90241532 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integrin alpha-V: beta-5 complex levels (ITGAV.ITGB5.4917.62.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integrin alpha-V: beta-5 complex measurement http://www.ebi.ac.uk/efo/EFO_0020480 GCST90241533 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Integrin beta-7 levels (ITGB7.11205.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 integrin beta-7 measurement http://www.ebi.ac.uk/efo/EFO_0802639 GCST90241534 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inter-alpha-trypsin inhibitor heavy chain H1 levels (ITIH1.7955.195.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 inter-alpha-trypsin inhibitor heavy chain H1 measurement http://www.ebi.ac.uk/efo/EFO_0801705 GCST90241535 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Inter-alpha-trypsin inhibitor heavy chain H5 levels (ITIH5.8233.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 inter-alpha-trypsin inhibitor heavy chain H5 measurement http://www.ebi.ac.uk/efo/EFO_0801706 GCST90241536 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intercellular adhesion molecule 1 levels (ICAM1.4342.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 intercellular adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0801707 GCST90241537 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intercellular adhesion molecule 2 levels (ICAM2.5486.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90241538 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intercellular adhesion molecule 3 levels (ICAM3.2649.77.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 intercellular adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020482 GCST90241539 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intercellular adhesion molecule 4 levels (ICAM4.6550.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 intercellular adhesion molecule 4 measurement http://www.ebi.ac.uk/efo/EFO_0801708 GCST90241540 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intercellular adhesion molecule 5 levels (ICAM5.8245.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90241541 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Intercellular adhesion molecule 5 levels (ICAM5.5124.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90241542 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-10 levels (IFNA10.14128.121.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-10 measurement http://www.ebi.ac.uk/efo/EFO_0021946 GCST90241543 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-10 levels (IFNA10.5733.61.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-10 measurement http://www.ebi.ac.uk/efo/EFO_0021946 GCST90241544 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-14 levels (IFNA14.7180.114.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-14 measurement http://www.ebi.ac.uk/efo/EFO_0802640 GCST90241545 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-4 levels (IFNA4.7268.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-4 measurement http://www.ebi.ac.uk/efo/EFO_0802641 GCST90241546 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-5 levels (IFNA5.6210.100.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802642 GCST90241547 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-6 levels (IFNA6.5714.88.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-6 measurement http://www.ebi.ac.uk/efo/EFO_0802643 GCST90241548 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-7 levels (IFNA7.14129.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-7 measurement http://www.ebi.ac.uk/efo/EFO_0021947 GCST90241549 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha-8 levels (IFNA8.6214.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon alpha-8 measurement http://www.ebi.ac.uk/efo/EFO_0802644 GCST90241550 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon alpha/beta receptor 1 levels (IFNAR1.9183.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interferon alpha/beta receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021850 GCST90241551 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon beta levels (IFNB1.7243.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon beta measurement http://www.ebi.ac.uk/efo/EFO_0802645 GCST90241552 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon gamma levels (IFNG.2989.17.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90241553 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon gamma levels (IFNG.14147.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90241554 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon gamma receptor 1 levels (IFNGR1.5825.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interferon gamma receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020484 GCST90241555 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon gamma receptor 2 levels (IFNGR2.8818.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90241557 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon gamma receptor 2 levels (IFNGR2.9305.89.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90241558 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon lambda-1 levels (IFNL1.4396.54.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon lambda-1 measurement http://www.ebi.ac.uk/efo/EFO_0020485 GCST90241560 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon lambda-2 levels (IFNL2.4397.26.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon lambda-2 measurement http://www.ebi.ac.uk/efo/EFO_0020486 GCST90241562 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon omega-1 levels (IFNW1.7196.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon omega-1 measurement http://www.ebi.ac.uk/efo/EFO_0802647 GCST90241563 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon regulatory factor 1 levels (IRF1.10009.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon regulatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021908 GCST90241564 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon regulatory factor 1 levels (IRF1.10351.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon regulatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021908 GCST90241565 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interferon regulatory factor 4 levels (IRF4.9857.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interferon regulatory factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0802648 GCST90241567 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 Receptor accessory protein levels (IL1RAP.14048.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-1 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0801711 GCST90241576 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 receptor antagonist protein levels (IL1RN.5353.89.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-1 receptor antagonist protein measurement http://www.ebi.ac.uk/efo/EFO_0801712 GCST90241577 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 receptor type 1 levels (IL1R1.2991.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90241578 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Interleukin-1 receptor type 2 levels (IL1R2.14133.93.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90241579 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane protein FLRT3 levels (FLRT3.13123.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90241773 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat transmembrane protein FLRT3 levels (FLRT3.9128.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90241774 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat-containing protein 15 levels (LRRC15.6557.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 leucine-rich repeat-containing protein 15 measurement http://www.ebi.ac.uk/efo/EFO_0801761 GCST90241775 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat-containing protein 19 levels (LRRC19.7014.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 leucine-rich repeat-containing protein 19 measurement http://www.ebi.ac.uk/efo/EFO_0801762 GCST90241776 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat-containing protein 3 levels (LRRC3.6917.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802698 GCST90241777 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat-containing protein 37A2 levels (LRRC37A2.8897.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat-containing protein 37A2 measurement http://www.ebi.ac.uk/efo/EFO_0802699 GCST90241778 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat-containing protein 4B levels (LRRC4B.11911.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat-containing protein 4B measurement http://www.ebi.ac.uk/efo/EFO_0802700 GCST90241779 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat-containing protein 4C levels (LRRC4C.9369.174.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat-containing protein 4C measurement http://www.ebi.ac.uk/efo/EFO_0802701 GCST90241780 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat-containing protein 74A levels (LRRC74A.8389.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 leucine-rich repeat-containing protein 74A measurement http://www.ebi.ac.uk/efo/EFO_0801763 GCST90241781 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 levels (LRIT2.11716.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802702 GCST90241782 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 levels (LRIT3.11534.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802703 GCST90241783 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 levels (LRIT3.11919.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802703 GCST90241784 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leucine-rich repeats and immunoglobulin-like domains protein 3 levels (LRIG3.3322.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 leucine-rich repeats and immunoglobulin-like domains protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020534 GCST90241785 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukemia inhibitory factor levels (LIF.7790.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 leukemia inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0801764 GCST90241786 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukemia inhibitory factor receptor levels (LIFR.5837.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90241787 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte cell-derived chemotaxin 1 levels (LECT1.9928.125.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukocyte cell-derived chemotaxin 1 measurement http://www.ebi.ac.uk/efo/EFO_0802704 GCST90241788 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily A member 4 levels (LILRA4.8299.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 leukocyte immunoglobulin-like receptor subfamily A member 4 measurement http://www.ebi.ac.uk/efo/EFO_0801765 GCST90241789 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily A member 5 levels (LILRA5.7787.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 leukocyte immunoglobulin-like receptor subfamily A member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801766 GCST90241790 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily A member 5 levels (LILRA5.8766.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukocyte immunoglobulin-like receptor subfamily A member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801766 GCST90241791 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily A member 6 levels (LILRA6.7059.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 8 leukocyte immunoglobulin-like receptor subfamily A member 6 measurement http://www.ebi.ac.uk/efo/EFO_0801767 GCST90241792 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 2 levels (LILRB2.5633.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90241794 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 3 levels (LILRB3.11334.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukocyte immunoglobulin-like receptor subfamily B member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802705 GCST90241796 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 5 levels (LILRB5.7015.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 leukocyte immunoglobulin-like receptor subfamily B member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801769 GCST90241798 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte surface antigen CD47 levels (CD47.6653.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukocyte surface antigen CD47 measurement http://www.ebi.ac.uk/efo/EFO_0022010 GCST90241799 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte-associated immunoglobulin-like receptor 1 levels (LAIR1.11284.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukocyte-associated immunoglobulin-like receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802706 GCST90241800 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte-specific transcript 1 protein levels (LST1.9531.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukocyte-specific transcript 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802707 GCST90241801 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukotriene A-4 hydrolase levels (LTA4H.3204.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukotriene a-4 hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020535 GCST90241802 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ligand-dependent nuclear receptor corepressor-like protein levels (LCORL.4304.18.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ligand-dependent nuclear receptor corepressor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020536 GCST90241803 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. LIM and cysteine-rich domains protein 1 levels (LMCD1.9530.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 LIM and cysteine-rich domains protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802708 GCST90241804 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Limbic system-associated membrane protein levels (LSAMP.2999.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 limbic system-associated membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0020537 GCST90241805 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Linker for activation of T-cells family member 1 levels (LAT.10551.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 linker for activation of T-cells family member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802709 GCST90241806 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Linker for activation of T-cells family member 2 levels (LAT2.5613.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 linker for activation of T-cells family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802710 GCST90241807 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lipase member K levels (LIPK.6413.79.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lipase member K measurement http://www.ebi.ac.uk/efo/EFO_0802711 GCST90241808 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lipase member N levels (LIPN.8097.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 lipase member N measurement http://www.ebi.ac.uk/efo/EFO_0801770 GCST90241809 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lipocalin-1 levels (LCN1.11708.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lipocalin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802712 GCST90241810 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lon protease homolog, mitochondrial levels (LONP1.6398.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lon protease homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801771 GCST90241811 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low affinity immunoglobulin epsilon Fc receptor levels (FCER2.3291.30.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 low affinity immunoglobulin epsilon Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0008210 GCST90241812 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low affinity immunoglobulin gamma Fc region receptor II-a levels (FCGR2A.3309.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 low affinity immunoglobulin gamma Fc region receptor II-a measurement http://www.ebi.ac.uk/efo/EFO_0021969 GCST90241813 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low affinity immunoglobulin gamma Fc region receptor II-b levels (FCGR2B.3310.62.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 8 low affinity immunoglobulin gamma Fc region receptor II-b measurement http://www.ebi.ac.uk/efo/EFO_0021970 GCST90241814 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low affinity immunoglobulin gamma Fc region receptor III-B levels (FCGR3B.3311.27.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 low affinity immunoglobulin gamma Fc region receptor III-B measurement http://www.ebi.ac.uk/efo/EFO_0008212 GCST90241815 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low molecular weight phosphotyrosine protein phosphatase levels (ACP1.3858.5.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90241816 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low-density lipoprotein receptor levels (LDLR.13129.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 low-density lipoprotein receptor measurement http://www.ebi.ac.uk/efo/EFO_0021937 GCST90241817 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low-density lipoprotein receptor-related protein 1, soluble levels (LRP1.8601.167.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 low-density lipoprotein receptor-related protein 1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0801772 GCST90241818 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low-density lipoprotein receptor-related protein 1, soluble levels (LRP1.9182.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 low-density lipoprotein receptor-related protein 1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0801772 GCST90241819 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low-density lipoprotein receptor-related protein 1B levels (LRP1B.11275.94.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 low-density lipoprotein receptor-related protein 1B measurement http://www.ebi.ac.uk/efo/EFO_0021873 GCST90241820 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low-density lipoprotein receptor-related protein 1B levels (LRP1B.7640.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 low-density lipoprotein receptor-related protein 1B measurement http://www.ebi.ac.uk/efo/EFO_0021873 GCST90241821 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Low-density lipoprotein receptor-related protein 8 levels (LRP8.3323.37.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 low-density lipoprotein receptor-related protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0020538 GCST90241822 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 1 levels (LILRB1.5090.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 11 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90241793 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 2 levels (LILRB2.5091.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90241795 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 4 levels (LILRB4.6453.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 leukocyte immunoglobulin-like receptor subfamily B member 4 measurement http://www.ebi.ac.uk/efo/EFO_0801768 GCST90241797 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lupus La protein levels (SSB.13526.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lupus La protein measurement http://www.ebi.ac.uk/efo/EFO_0802713 GCST90241823 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lupus La protein levels (SSB.13625.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lupus La protein measurement http://www.ebi.ac.uk/efo/EFO_0802713 GCST90241824 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Luteinizing hormone levels (CGA.LHB.2953.31.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90241825 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lutropin subunit beta levels (LHB.8376.25.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lutropin subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801773 GCST90241826 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ly6/PLAUR domain-containing protein 3 levels (LYPD3.13107.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Ly6/PLAUR domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0021931 GCST90241827 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphocyte activation gene 3 protein levels (LAG3.5099.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphocyte activation gene 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0020540 GCST90241828 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphocyte activation gene 3 protein levels (LAG3.9950.229.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphocyte activation gene 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0020540 GCST90241829 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphocyte antigen 6 complex locus protein G6c levels (LY6G6C.6256.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lymphocyte antigen 6 complex locus protein G6c measurement http://www.ebi.ac.uk/efo/EFO_0801774 GCST90241830 Genome-wide genotyping array 2022-04-07 34871961 McHenry ML 2021-12-03 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34871961 Resistance to TST/IGRA conversion in Uganda: Heritability and Genome-Wide Association Study. Pulmonary tuberculosis resistance 74 African ancestry cases, 189 African ancestry controls NA Illumina [733040] 6 susceptibility to Mycobacterium tuberculosis infection measurement http://www.ebi.ac.uk/efo/EFO_0008407 GCST90101740 Genome-wide genotyping array 2022-05-12 35204431 Park S 2022-01-28 Diagnostics (Basel) www.ncbi.nlm.nih.gov/pubmed/35204431 Polygenetic Variants Related to Osteoarthritis Risk and Their Interactions with Energy, Protein, Fat, and Alcohol Intake in Adults in a Large Cohort. Osteoarthritis 580 East Asian ancestry cases, 4,850 East Asian ancestry controls NA Affymetrix [NR] 3 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90102548 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 1) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 16 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007181 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 2) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 14 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007182 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 3) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 6 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007183 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 4) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007184 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 5) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 6 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007185 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 51) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007231 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 52) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007232 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 53) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 3 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007233 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 54) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007234 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 55) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007235 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 56) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007236 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 57) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007237 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 58) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007238 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 59) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007239 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 60) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007240 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 61) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 3 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007241 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 62) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007242 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 63) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007243 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 1) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 4 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007244 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 2) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 8 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007245 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 3) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007246 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 4) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007247 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 5) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007248 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 6) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007249 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 7) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007250 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 8) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007251 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 9) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007252 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 10) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007253 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 11) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 5 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007254 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 12) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007255 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 13) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007256 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 14) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007257 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 15) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007258 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 16) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007259 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 17) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007260 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 18) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 4 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007261 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 19) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007262 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 20) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007263 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 21) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007264 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 22) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007265 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 23) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007266 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 24) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007267 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 25) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007268 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 26) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007269 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 27) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007270 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 28) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007271 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 29) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007272 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 30) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 5 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007273 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 31) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007274 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 32) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007275 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 33) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007276 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 34) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007277 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 35) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007278 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 36) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007279 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 37) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007280 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 6) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007186 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 7) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 7 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007187 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 8) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007188 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 9) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 5 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007189 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 10) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007190 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 11) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 10 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007191 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 12) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007192 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 13) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007193 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 14) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007194 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 15) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90007195 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 16) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007196 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 17) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007197 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 18) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007198 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 19) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007199 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 20) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007200 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 21) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007201 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 22) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007202 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 23) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007203 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 24) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007204 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 25) 4,680 European ancestry individuals 3,566 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007205 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 38) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007281 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 39) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90007282 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 40) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007283 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 41) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007284 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 42) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007285 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 43) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007286 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 44) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007287 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 45) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007288 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 46) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007289 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 47) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90007290 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 48) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007291 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 49) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007292 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 50) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007293 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 51) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007294 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 52) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007295 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 53) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 4 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007296 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 54) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007297 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 55) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90007298 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 56) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007299 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 57) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007300 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 58) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007301 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 59) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007302 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 60) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007303 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 61) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007304 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 62) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 3 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007305 Genome-wide genotyping array 2021-12-14 33288918 White JD 2020-12-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33288918 Insights into the genetic architecture of the human face. Facial morphology (segment 63) 3,566 European ancestry individuals 4,680 European ancestry individuals Illumina [7417619] (imputed) 2 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90007306 Genome-wide genotyping array 2022-08-04 35505052 Fan CC 2022-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35505052 Multivariate genome-wide association study on tissue-sensitive diffusion metrics highlights pathways that shape the human brain. Whole brain restricted isotropic diffusion (multivariate analysis) 23,543 European ancestry individuals 11,555 European ancestry individuals, 3,030 non-European ancestry individuals NR [NR] (imputed) 291 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90131904 Genome-wide genotyping array 2022-08-04 35505052 Fan CC 2022-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35505052 Multivariate genome-wide association study on tissue-sensitive diffusion metrics highlights pathways that shape the human brain. Whole brain restricted directional diffusion (multivariate analysis) 23,543 European ancestry individuals 11,555 European ancestry individuals, 3,030 non-European ancestry individuals NR [NR] (imputed) 257 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90131905 Genome-wide genotyping array 2022-08-04 35505052 Fan CC 2022-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35505052 Multivariate genome-wide association study on tissue-sensitive diffusion metrics highlights pathways that shape the human brain. Whole brain free water diffusion (multivariate analysis) 23,543 European ancestry individuals 11,555 European ancestry individuals, 3,030 non-European ancestry individuals NR [NR] (imputed) 199 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90131906 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 134 levels (DEFB134.10610.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 134 measurement http://www.ebi.ac.uk/efo/EFO_0802327 GCST90240431 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 135 levels (DEFB135.6411.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 135 measurement http://www.ebi.ac.uk/efo/EFO_0802328 GCST90240432 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 136 levels (DEFB136.9332.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 136 measurement http://www.ebi.ac.uk/efo/EFO_0802329 GCST90240433 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-endorphin levels (POMC.2558.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90240434 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-endorphin levels (POMC.4890.10.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90240435 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-galactoside alpha-2,6-sialyltransferase 1 levels (ST6GAL1.6035.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-galactoside alpha-2,6-sialyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802330 GCST90240436 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-mannosidase levels (MANBA.6382.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 beta-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801421 GCST90240437 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-microseminoprotein levels (MSMB.10620.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 beta-microseminoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020955 GCST90240438 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. beta-nerve growth factor levels (NGF.5801.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST90240439 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-sarcoglycan levels (SGCB.7034.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 beta-sarcoglycan measurement http://www.ebi.ac.uk/efo/EFO_0801422 GCST90240440 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-soluble NSF attachment protein levels (NAPB.12655.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 beta-soluble NSF attachment protein measurement http://www.ebi.ac.uk/efo/EFO_0801423 GCST90240441 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BH3-interacting domain death agonist levels (BID.5798.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BH3-interacting domain death agonist measurement http://www.ebi.ac.uk/efo/EFO_0021994 GCST90240442 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1 levels (PAPSS1.14007.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802331 GCST90240443 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1 levels (NDST1.6927.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802332 GCST90240444 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bifunctional polynucleotide phosphatase/kinase levels (PNKP.13657.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 bifunctional polynucleotide phosphatase/kinase measurement http://www.ebi.ac.uk/efo/EFO_0801424 GCST90240445 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Biglycan levels (BGN.13690.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 biglycan measurement http://www.ebi.ac.uk/efo/EFO_0020182 GCST90240446 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Biglycan levels (BGN.3284.75.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 biglycan measurement http://www.ebi.ac.uk/efo/EFO_0020182 GCST90240447 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bile salt sulfotransferase levels (SULT2A1.9829.91.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bile salt sulfotransferase measurement http://www.ebi.ac.uk/efo/EFO_0802333 GCST90240448 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bile salt-activated lipase levels (CEL.9796.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 bile salt-activated lipase measurement http://www.ebi.ac.uk/efo/EFO_0801425 GCST90240449 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Biliverdin reductase A levels (BLVRA.11382.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 biliverdin reductase A measurement http://www.ebi.ac.uk/efo/EFO_0801426 GCST90240450 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bis(5'-adenosyl)-triphosphatase levels (FHIT.9826.135.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 bis(5'-adenosyl)-triphosphatase measurement http://www.ebi.ac.uk/efo/EFO_0801427 GCST90240451 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bisphosphoglycerate mutase levels (BPGM.12020.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bisphosphoglycerate mutase measurement http://www.ebi.ac.uk/efo/EFO_0802334 GCST90240452 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BMP-binding endothelial regulator protein levels (BMPER.3654.27.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BMP-binding endothelial regulator protein measurement http://www.ebi.ac.uk/efo/EFO_0020183 GCST90240453 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BolA-like protein 2 levels (BOLA2.8404.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bolA-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802335 GCST90240454 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bombesin receptor-activated protein C6orf89 levels (C6orf89.10885.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 bombesin receptor-activated protein C6orf89 measurement http://www.ebi.ac.uk/efo/EFO_0801428 GCST90240455 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-1,4-glucuronyltransferase 1 levels (B3GNT1.8259.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 beta-1,4-glucuronyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801412 GCST90240406 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. beta-adrenergic receptor kinase 1 levels (ADRBK1.3347.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-adrenergic receptor kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020181 GCST90240407 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-arrestin-1 levels (ARRB1.12643.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-arrestin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801413 GCST90240408 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-crystallin B2 levels (CRYBB2.10000.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-crystallin B2 measurement http://www.ebi.ac.uk/efo/EFO_0801414 GCST90240409 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 1 levels (DEFB1.6629.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 beta-defensin 1 measurement http://www.ebi.ac.uk/efo/EFO_0801415 GCST90240410 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 103 levels (DEFB103A.5679.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 103 measurement http://www.ebi.ac.uk/efo/EFO_0802315 GCST90240411 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 104 levels (DEFB104A.5763.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-defensin 104 measurement http://www.ebi.ac.uk/efo/EFO_0801416 GCST90240412 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 105 levels (DEFB105A.10962.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-defensin 105 measurement http://www.ebi.ac.uk/efo/EFO_0801417 GCST90240413 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 106 levels (DEFB106A.5664.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 106 measurement http://www.ebi.ac.uk/efo/EFO_0802316 GCST90240414 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 107 levels (DEFB107A.6399.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 107 measurement http://www.ebi.ac.uk/efo/EFO_0802317 GCST90240415 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 108B levels (DEFB108B.5611.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 108B measurement http://www.ebi.ac.uk/efo/EFO_0802318 GCST90240416 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 110 levels (DEFB110.8340.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 110 measurement http://www.ebi.ac.uk/efo/EFO_0802319 GCST90240417 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 112 levels (DEFB112.5689.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-defensin 112 measurement http://www.ebi.ac.uk/efo/EFO_0801418 GCST90240418 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 113 levels (DEFB113.13374.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 113 measurement http://www.ebi.ac.uk/efo/EFO_0802320 GCST90240419 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 115 levels (DEFB115.8391.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 115 measurement http://www.ebi.ac.uk/efo/EFO_0802321 GCST90240420 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 116 levels (DEFB116.11144.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 116 measurement http://www.ebi.ac.uk/efo/EFO_0802322 GCST90240421 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 118 levels (DEFB118.9306.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 118 measurement http://www.ebi.ac.uk/efo/EFO_0802323 GCST90240422 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 119 levels (DEFB119.13455.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 beta-defensin 119 measurement http://www.ebi.ac.uk/efo/EFO_0801419 GCST90240423 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 119 levels (DEFB119.10689.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 119 measurement http://www.ebi.ac.uk/efo/EFO_0801419 GCST90240424 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 119 levels (DEFB119.8315.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 119 measurement http://www.ebi.ac.uk/efo/EFO_0801419 GCST90240425 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 119 levels (DEFB119.8370.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 119 measurement http://www.ebi.ac.uk/efo/EFO_0801419 GCST90240426 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 121 levels (DEFB121.5765.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 121 measurement http://www.ebi.ac.uk/efo/EFO_0802324 GCST90240427 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 123 levels (DEFB123.9362.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 123 measurement http://www.ebi.ac.uk/efo/EFO_0802325 GCST90240428 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 125 levels (DEFB125.9486.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 beta-defensin 125 measurement http://www.ebi.ac.uk/efo/EFO_0802326 GCST90240429 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Beta-defensin 128 levels (DEFB128.6360.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 beta-defensin 128 measurement http://www.ebi.ac.uk/efo/EFO_0801420 GCST90240430 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zona pellucida-like domain-containing protein 1 levels (ZPLD1.5590.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zona pellucida-like domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803290 GCST90243399 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. FAS-associated factor 2 levels (FAF2.8761.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fAS-associated factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0802541 GCST90243400 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class F member 2 levels (SCARF2.9925.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90243401 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphocyte antigen 6 complex locus protein G6d levels (LY6G6D.6469.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphocyte antigen 6 complex locus protein G6d measurement http://www.ebi.ac.uk/efo/EFO_0802714 GCST90241831 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphocyte antigen 86 levels (LY86.3623.84.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphocyte antigen 86 measurement http://www.ebi.ac.uk/efo/EFO_0020541 GCST90241832 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphocyte function-associated antigen 3 levels (CD58.10938.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphocyte function-associated antigen 3 measurement http://www.ebi.ac.uk/efo/EFO_0802715 GCST90241833 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphoid-restricted membrane protein levels (LRMP.10704.91.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphoid-restricted membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0802716 GCST90241834 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphotactin levels (XCL1.14078.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 lymphotactin measurement http://www.ebi.ac.uk/efo/EFO_0008214 GCST90241835 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphotactin levels (XCL1.4143.74.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphotactin measurement http://www.ebi.ac.uk/efo/EFO_0008214 GCST90241836 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphotoxin alpha2:beta1 levels (LTA.LTB.3506.49.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphotoxin alpha2:beta1 measurement http://www.ebi.ac.uk/efo/EFO_0020543 GCST90241837 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lymphotoxin-alpha levels (LTA.4703.87.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lymphotoxin-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020544 GCST90241838 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. LysM and putative peptidoglycan-binding domain-containing protein 3 levels (LYSMD3.10563.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lysM and putative peptidoglycan-binding domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802717 GCST90241839 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. LysM and putative peptidoglycan-binding domain-containing protein 4 levels (LYSMD4.9106.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lysM and putative peptidoglycan-binding domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802718 GCST90241840 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysophosphatidylcholine acyltransferase 2 levels (LPCAT2.11175.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lysophosphatidylcholine acyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801775 GCST90241841 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysophospholipase-like protein 1 levels (LYPLAL1.12428.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lysophospholipase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802719 GCST90241842 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysosomal acid phosphatase levels (ACP2.9237.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 lysosomal acid phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0801776 GCST90241843 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysosomal Pro-X carboxypeptidase levels (PRCP.5722.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 lysosomal Pro-X carboxypeptidase measurement http://www.ebi.ac.uk/efo/EFO_0801777 GCST90241844 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysosomal protective protein levels (CTSA.3179.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90241845 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysosome membrane protein 2 levels (SCARB2.5100.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lysosome membrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020545 GCST90241846 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysosome-associated membrane glycoprotein 3 levels (LAMP3.9355.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lysosome-associated membrane glycoprotein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802720 GCST90241847 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysozyme C levels (LYZ.4920.10.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90241848 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysozyme g-like protein 1 levels (LYG1.9243.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 lysozyme g-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801778 GCST90241849 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysozyme-like protein 2 levels (LYZL2.6377.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 lysozyme-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801779 GCST90241850 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Lysyl oxidase homolog 2 levels (LOXL2.6504.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 lysyl oxidase homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0802721 GCST90241851 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. M-phase inducer phosphatase 2 levels (CDC25B.12427.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 m-phase inducer phosphatase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801780 GCST90241852 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Voltage-gated potassium channel subunit beta-2 levels (KCNAB2.10015.119.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 voltage-gated potassium channel subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0802219 GCST90243349 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. von Willebrand factor C domain-containing protein 2-like levels (VWC2L.7995.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 von Willebrand factor C domain-containing protein 2-like measurement http://www.ebi.ac.uk/efo/EFO_0803259 GCST90243350 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP four-disulfide core domain protein 10A levels (WFDC10A.13429.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WAP four-disulfide core domain protein 10A measurement http://www.ebi.ac.uk/efo/EFO_0803260 GCST90243351 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP four-disulfide core domain protein 12 levels (WFDC12.6037.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WAP four-disulfide core domain protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0803261 GCST90243352 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP four-disulfide core domain protein 13 levels (WFDC13.9345.436.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WAP four-disulfide core domain protein 13 measurement http://www.ebi.ac.uk/efo/EFO_0803262 GCST90243353 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP four-disulfide core domain protein 2 levels (WFDC2.11388.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WAP four-disulfide core domain protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803263 GCST90243354 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP four-disulfide core domain protein 3 levels (WFDC3.6384.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 WAP four-disulfide core domain protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802220 GCST90243355 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP four-disulfide core domain protein 5 levels (WFDC5.6969.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WAP four-disulfide core domain protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803264 GCST90243356 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP, kazal, immunoglobulin, kunitz and NTR domain-containing protein 1 levels (WFIKKN1.3191.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 wap, kazal, immunoglobulin, kunitz and ntr domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020852 GCST90243357 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 levels (WFIKKN2.13408.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90243358 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 levels (WFIKKN2.3235.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90243359 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WD repeat-containing protein 1 levels (WDR1.10723.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 WD repeat-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802221 GCST90243360 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Wnt inhibitory factor 1 levels (WIF1.2848.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 wnt inhibitory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020853 GCST90243361 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WNT1-inducible-signaling pathway protein 1 levels (WISP1.13692.154.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 WNT1-inducible-signaling pathway protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008321 GCST90243362 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WNT1-inducible-signaling pathway protein 3 levels (WISP3.5927.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 WNT1-inducible-signaling pathway protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0022003 GCST90243363 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WSC domain-containing protein 2 levels (WSCD2.6274.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 WSC domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802222 GCST90243364 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WW domain binding protein 1-like levels (WBP1L.9532.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WW domain binding protein 1-like measurement http://www.ebi.ac.uk/efo/EFO_0803265 GCST90243365 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. WW domain-binding protein 1 levels (WBP1.10943.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 WW domain-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803266 GCST90243366 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. X-linked interleukin-1 receptor accessory protein-like 2 levels (IL1RAPL2.5082.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 x-linked interleukin-1 receptor accessory protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0020854 GCST90243367 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Xaa-Pro aminopeptidase 1 levels (XPNPEP1.3481.87.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 xaa-pro aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020856 GCST90243368 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Xanthine dehydrogenase/oxidase levels (XDH.11264.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 xanthine dehydrogenase/oxidase measurement http://www.ebi.ac.uk/efo/EFO_0803267 GCST90243369 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Xyloside xylosyltransferase 1 levels (XXYLT1.6375.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 xyloside xylosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802223 GCST90243370 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Y-box-binding protein 2 levels (YBX2.6372.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 y-box-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802224 GCST90243371 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. YTH domain-containing protein 1 levels (YTHDC1.8878.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 YTH domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803268 GCST90243372 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 10 levels (ZNF10.11567.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0803270 GCST90243373 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular endothelial growth factor receptor 3 levels (FLT4.2358.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90243324 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Versican core protein levels (VCAN.9561.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 versican core protein measurement http://www.ebi.ac.uk/efo/EFO_0803248 GCST90243325 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Very long-chain acyl-CoA synthetase levels (SLC27A2.9045.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 very long-chain acyl-CoA synthetase measurement http://www.ebi.ac.uk/efo/EFO_0802211 GCST90243326 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle transport protein USE1 levels (USE1.8057.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle transport protein USE1 measurement http://www.ebi.ac.uk/efo/EFO_0803249 GCST90243327 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle transport through interaction with t-SNAREs homolog 1A levels (VTI1A.7952.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle transport through interaction with t-SNAREs homolog 1A measurement http://www.ebi.ac.uk/efo/EFO_0803250 GCST90243328 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle transport through interaction with t-SNAREs homolog 1B levels (VTI1B.8963.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vesicle transport through interaction with t-SNAREs homolog 1B measurement http://www.ebi.ac.uk/efo/EFO_0802212 GCST90243329 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-associated membrane protein 3 levels (VAMP3.7903.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle-associated membrane protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803251 GCST90243330 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-associated membrane protein 4 levels (VAMP4.7732.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle-associated membrane protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803252 GCST90243331 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-associated membrane protein 5 levels (VAMP5.8290.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle-associated membrane protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803253 GCST90243332 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-associated membrane protein 8 levels (VAMP8.7064.2.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle-associated membrane protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0803254 GCST90243333 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-associated membrane protein-associated protein A levels (VAPA.7167.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vesicle-associated membrane protein-associated protein A measurement http://www.ebi.ac.uk/efo/EFO_0802213 GCST90243334 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-associated membrane protein-associated protein B/C levels (VAPB.7181.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle-associated membrane protein-associated protein B/C measurement http://www.ebi.ac.uk/efo/EFO_0803255 GCST90243335 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-fusing ATPase levels (NSF.13992.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vesicle-fusing ATPase measurement http://www.ebi.ac.uk/efo/EFO_0802214 GCST90243336 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicle-trafficking protein SEC22a levels (SEC22A.13713.164.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicle-trafficking protein SEC22a measurement http://www.ebi.ac.uk/efo/EFO_0803256 GCST90243337 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicular integral-membrane protein VIP36 levels (LMAN2.7638.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicular integral-membrane protein VIP36 measurement http://www.ebi.ac.uk/efo/EFO_0022012 GCST90243338 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vesicular integral-membrane protein VIP36 levels (LMAN2.9468.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vesicular integral-membrane protein VIP36 measurement http://www.ebi.ac.uk/efo/EFO_0022012 GCST90243339 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vigilin levels (HDLBP.13570.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vigilin measurement http://www.ebi.ac.uk/efo/EFO_0802215 GCST90243340 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vinculin levels (VCL.8750.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vinculin measurement http://www.ebi.ac.uk/efo/EFO_0803257 GCST90243341 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vinexin b levels (SORBS3.12976.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vinexin b measurement http://www.ebi.ac.uk/efo/EFO_0803258 GCST90243342 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. VIP36-like protein levels (LMAN2L.8013.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 VIP36-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802216 GCST90243343 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vitamin D-binding protein levels (GC.6581.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST90243344 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vitrin levels (VIT.6234.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 vitrin measurement http://www.ebi.ac.uk/efo/EFO_0802217 GCST90243345 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vitronectin levels (VTN.8280.238.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90243346 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vitronectin levels (VTN.13125.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90243347 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Voltage-dependent calcium channel subunit alpha-2/delta-3 levels (CACNA2D3.8885.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 voltage-dependent calcium channel subunit alpha-2/delta-3 measurement http://www.ebi.ac.uk/efo/EFO_0802218 GCST90243348 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 134 levels (ZNF134.12787.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 134 measurement http://www.ebi.ac.uk/efo/EFO_0803271 GCST90243374 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 174 levels (ZNF174.11486.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 174 measurement http://www.ebi.ac.uk/efo/EFO_0803272 GCST90243375 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 175 levels (ZNF175.12716.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 zinc finger protein 175 measurement http://www.ebi.ac.uk/efo/EFO_0802225 GCST90243376 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 18 levels (ZNF18.11372.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 zinc finger protein 18 measurement http://www.ebi.ac.uk/efo/EFO_0802226 GCST90243377 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 180 levels (ZNF180.12771.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 180 measurement http://www.ebi.ac.uk/efo/EFO_0803273 GCST90243378 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 23 levels (ZNF23.11565.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 23 measurement http://www.ebi.ac.uk/efo/EFO_0803274 GCST90243379 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 264 levels (ZNF264.9993.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 264 measurement http://www.ebi.ac.uk/efo/EFO_0803275 GCST90243380 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 276 levels (ZNF276.14692.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 zinc finger protein 276 measurement http://www.ebi.ac.uk/efo/EFO_0802227 GCST90243381 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 329 levels (ZNF329.12803.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 329 measurement http://www.ebi.ac.uk/efo/EFO_0803276 GCST90243382 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 334 levels (ZNF334.12763.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 334 measurement http://www.ebi.ac.uk/efo/EFO_0803277 GCST90243383 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 358 levels (ZNF358.10529.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 358 measurement http://www.ebi.ac.uk/efo/EFO_0803278 GCST90243384 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 382 levels (ZNF382.14616.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 382 measurement http://www.ebi.ac.uk/efo/EFO_0803279 GCST90243385 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 410 levels (ZNF410.12843.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 410 measurement http://www.ebi.ac.uk/efo/EFO_0803280 GCST90243386 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 415 levels (ZNF415.12811.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 415 measurement http://www.ebi.ac.uk/efo/EFO_0803281 GCST90243387 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 566 levels (ZNF566.12795.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 566 measurement http://www.ebi.ac.uk/efo/EFO_0803282 GCST90243388 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 75D levels (ZNF75D.11596.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 75D measurement http://www.ebi.ac.uk/efo/EFO_0803283 GCST90243389 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 774 levels (ZNF774.12760.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 774 measurement http://www.ebi.ac.uk/efo/EFO_0803284 GCST90243390 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein 843 levels (ZNF843.8321.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein 843 measurement http://www.ebi.ac.uk/efo/EFO_0803285 GCST90243391 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc finger protein SNAI2 levels (SNAI2.10014.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc finger protein SNAI2 measurement http://www.ebi.ac.uk/efo/EFO_0803286 GCST90243392 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc fingers and homeoboxes protein 3 levels (ZHX3.10036.201.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 zinc fingers and homeoboxes protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803299 GCST90243393 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc transporter 3 levels (SLC30A3.9081.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc transporter 3 measurement http://www.ebi.ac.uk/efo/EFO_0803287 GCST90243394 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc transporter 5 levels (SLC30A5.9594.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc transporter 5 measurement http://www.ebi.ac.uk/efo/EFO_0803288 GCST90243395 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc-alpha-2-glycoprotein levels (AZGP1.9312.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 zinc-alpha-2-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0802228 GCST90243396 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zinc/RING finger protein 4 levels (ZNRF4.9467.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 zinc/RING finger protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803289 GCST90243397 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Zona pellucida sperm-binding protein 4 levels (ZP4.7766.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 zona pellucida sperm-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802229 GCST90243398 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Erythropoietin receptor levels (EPOR.2715.25.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 erythropoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020364 GCST90241107 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ES1 protein homolog, mitochondrial levels (C21orf33.5981.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ES1 protein homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802529 GCST90241108 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Essential MCU regulator, mitochondrial levels (SMDT1.9497.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 essential MCU regulator, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802530 GCST90241109 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Estradiol 17-beta-dehydrogenase 1 levels (HSD17B1.4708.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 estradiol 17-beta-dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020365 GCST90241110 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Estradiol 17-beta-dehydrogenase 2 levels (HSD17B2.8979.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 estradiol 17-beta-dehydrogenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802531 GCST90241111 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Estrogen receptor levels (ESR1.2945.25.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 estrogen receptor measurement http://www.ebi.ac.uk/efo/EFO_0008125 GCST90241112 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Estrogen sulfotransferase levels (SULT1E1.9878.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 estrogen sulfotransferase measurement http://www.ebi.ac.uk/efo/EFO_0801586 GCST90241113 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ethanolamine kinase 1 levels (ETNK1.8328.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ethanolamine kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802532 GCST90241114 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ETS domain-containing protein Elk-1 levels (ELK1.10006.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ETS domain-containing protein Elk-1 measurement http://www.ebi.ac.uk/efo/EFO_0801587 GCST90241115 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ETS domain-containing protein Elk-3 levels (ELK3.5707.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ETS domain-containing protein Elk-3 measurement http://www.ebi.ac.uk/efo/EFO_0801588 GCST90241116 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ETS homologous factor levels (EHF.13387.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ETS homologous factor measurement http://www.ebi.ac.uk/efo/EFO_0802533 GCST90241117 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ETS-related transcription factor Elf-5 levels (ELF5.13457.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ETS-related transcription factor Elf-5 measurement http://www.ebi.ac.uk/efo/EFO_0802534 GCST90241118 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic initiation factor 4A-III levels (EIF4A3.4997.19.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic initiation factor 4a-III measurement http://www.ebi.ac.uk/efo/EFO_0020366 GCST90241119 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 1A, X-chromosomal levels (EIF1AX.9850.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic translation initiation factor 1A, X-chromosomal measurement http://www.ebi.ac.uk/efo/EFO_0801589 GCST90241120 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 3 subunit G levels (EIF3G.11454.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic translation initiation factor 3 subunit G measurement http://www.ebi.ac.uk/efo/EFO_0801590 GCST90241121 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 3 subunit J levels (EIF3J.13497.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic translation initiation factor 3 subunit J measurement http://www.ebi.ac.uk/efo/EFO_0801591 GCST90241122 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 4 gamma 3 levels (EIF4G3.13991.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 eukaryotic translation initiation factor 4 gamma 3 measurement http://www.ebi.ac.uk/efo/EFO_0802535 GCST90241123 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 4B levels (EIF4B.14675.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic translation initiation factor 4B measurement http://www.ebi.ac.uk/efo/EFO_0801592 GCST90241124 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 4E type 2 levels (EIF4E2.9745.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic translation initiation factor 4E type 2 measurement http://www.ebi.ac.uk/efo/EFO_0801593 GCST90241125 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 4E-binding protein 2 levels (EIF4EBP2.4184.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 eukaryotic translation initiation factor 4E-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020368 GCST90241126 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 5 levels (EIF5.2612.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic translation initiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020369 GCST90241127 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eukaryotic translation initiation factor 5A-1 levels (EIF5A.5888.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 eukaryotic translation initiation factor 5A-1 measurement http://www.ebi.ac.uk/efo/EFO_0020370 GCST90241128 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Exosome complex component CSL4 levels (EXOSC1.7930.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 exosome complex component CSL4 measurement http://www.ebi.ac.uk/efo/EFO_0802536 GCST90241129 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Exosome complex component RRP40 levels (EXOSC3.12605.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 exosome complex component RRP40 measurement http://www.ebi.ac.uk/efo/EFO_0801594 GCST90241130 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Exostosin-like 2 levels (EXTL2.6528.95.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 exostosin-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801595 GCST90241131 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibronectin type III domain-containing protein 5 levels (FNDC5.8041.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fibronectin type III domain-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801601 GCST90241182 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibulin-1 levels (FBLN1.6470.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibulin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802550 GCST90241183 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ficolin-1 levels (FCN1.3613.62.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90241184 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ficolin-2 levels (FCN2.3313.21.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 ficolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008135 GCST90241185 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Filamin-A levels (FLNA.11124.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 filamin-A measurement http://www.ebi.ac.uk/efo/EFO_0801602 GCST90241186 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Filamin-A levels (FLNA.11170.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 filamin-A measurement http://www.ebi.ac.uk/efo/EFO_0801602 GCST90241187 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Filamin-A levels (FLNA.12906.137.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 filamin-A measurement http://www.ebi.ac.uk/efo/EFO_0801602 GCST90241188 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Filamin-A levels (FLNA.11108.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 filamin-A measurement http://www.ebi.ac.uk/efo/EFO_0801602 GCST90241189 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Flap endonuclease 1 levels (FEN1.12577.100.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 flap endonuclease 1 measurement http://www.ebi.ac.uk/efo/EFO_0802551 GCST90241190 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fms-related tyrosine kinase 3 ligand levels (FLT3LG.14093.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90241191 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fms-related tyrosine kinase 3 ligand levels (FLT3LG.3053.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90241192 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Follicle stimulating hormone levels (CGA.FSHB.3032.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90241193 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Follistatin levels (FST.4132.27.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 follistatin measurement http://www.ebi.ac.uk/efo/EFO_0010614 GCST90241194 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Follistatin-related protein 1 levels (FSTL1.13112.179.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 follistatin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021934 GCST90241195 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Follistatin-related protein 1 levels (FSTL1.9304.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 follistatin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021934 GCST90241196 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Follistatin-related protein 3 levels (FSTL3.3438.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 follistatin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020394 GCST90241197 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Follistatin-related protein 4 levels (FSTL4.9350.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 follistatin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801603 GCST90241198 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Follistatin-related protein 5 levels (FSTL5.7099.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 follistatin-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802552 GCST90241199 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Forkhead box protein C2 levels (FOXC2.14051.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 forkhead box protein C2 measurement http://www.ebi.ac.uk/efo/EFO_0802553 GCST90241200 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Forkhead box protein J2 levels (FOXJ2.14204.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 forkhead box protein J2 measurement http://www.ebi.ac.uk/efo/EFO_0801604 GCST90241201 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Forkhead box protein L2 levels (FOXL2.11375.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 forkhead box protein L2 measurement http://www.ebi.ac.uk/efo/EFO_0802554 GCST90241202 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Four-jointed box protein 1 levels (FJX1.7921.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 four-jointed box protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801605 GCST90241203 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fractalkine levels (CX3CL1.2827.23.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fractalkine measurement http://www.ebi.ac.uk/efo/EFO_0020395 GCST90241204 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fragile X mental retardation syndrome-related protein 1 levels (FXR1.13076.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fragile X mental retardation syndrome-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802555 GCST90241205 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fructose-1,6-bisphosphatase 1 levels (FBP1.7206.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fructose-1,6-bisphosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801606 GCST90241206 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-B1 levels (EFNB1.5746.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ephrin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0021930 GCST90241082 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-B1 levels (EFNB1.13104.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0021930 GCST90241083 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-B2 levels (EFNB2.14131.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0802526 GCST90241084 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-B2 levels (EFNB2.8772.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0802526 GCST90241085 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-B3 levels (EFNB3.7785.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90241086 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-B3 levels (EFNB3.2514.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90241087 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epidermal growth factor levels (EGF.5509.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90241088 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epidermal growth factor receptor levels (EGFR.2677.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90241089 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epidermal growth factor receptor levels (EGFR.5328.33.37) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90241090 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epidermal growth factor receptor substrate 15-like 1 levels (EPS15L1.4212.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 epidermal growth factor receptor substrate 15-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020360 GCST90241091 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epididymal secretory protein E1 levels (NPC2.6259.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 epididymal secretory protein E1 measurement http://www.ebi.ac.uk/efo/EFO_0801575 GCST90241092 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epididymal secretory protein E3-beta levels (EDDM3B.7782.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 epididymal secretory protein E3-beta measurement http://www.ebi.ac.uk/efo/EFO_0802527 GCST90241093 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epididymal-specific lipocalin-10 levels (LCN10.13007.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 epididymal-specific lipocalin-10 measurement http://www.ebi.ac.uk/efo/EFO_0801576 GCST90241094 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epididymal-specific lipocalin-8 levels (LCN8.5643.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 epididymal-specific lipocalin-8 measurement http://www.ebi.ac.uk/efo/EFO_0802528 GCST90241095 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epididymis-specific alpha-mannosidase levels (MAN2B2.9251.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 epididymis-specific alpha-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801577 GCST90241096 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epiphycan levels (EPYC.9278.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 epiphycan measurement http://www.ebi.ac.uk/efo/EFO_0801578 GCST90241097 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Epiregulin levels (EREG.4956.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 epiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020361 GCST90241098 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ER membrane protein complex subunit 1 levels (EMC1.11989.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ER membrane protein complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0801579 GCST90241099 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ER membrane protein complex subunit 4 levels (EMC4.13516.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 ER membrane protein complex subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0801580 GCST90241100 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Erlin-1 levels (ERLIN1.8776.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 erlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801581 GCST90241101 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ERO1-like protein alpha levels (ERO1L.7060.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ERO1-like protein alpha measurement http://www.ebi.ac.uk/efo/EFO_0801582 GCST90241102 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ERO1-like protein beta levels (ERO1LB.7994.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ERO1-like protein beta measurement http://www.ebi.ac.uk/efo/EFO_0801583 GCST90241103 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Erythrocyte band 7 integral membrane protein levels (STOM.8261.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 erythrocyte band 7 integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801584 GCST90241104 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Erythroid membrane-associated protein levels (ERMAP.8631.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 erythroid membrane-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801585 GCST90241105 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Erythropoietin levels (EPO.5813.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 erythropoietin measurement http://www.ebi.ac.uk/efo/EFO_0020363 GCST90241106 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Extracellular sulfatase Sulf-2 levels (SULF2.8305.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 extracellular sulfatase Sulf-2 measurement http://www.ebi.ac.uk/efo/EFO_0801596 GCST90241132 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Extracellular superoxide dismutase [Cu-Zn] levels (SOD3.8463.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 extracellular superoxide dismutase [Cu-Zn] measurement http://www.ebi.ac.uk/efo/EFO_0022018 GCST90241133 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ezrin levels (EZR.9753.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ezrin measurement http://www.ebi.ac.uk/efo/EFO_0801597 GCST90241134 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. F-box only protein 3 levels (FBXO3.14628.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 f-box only protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802537 GCST90241135 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. F-box/LRR-repeat protein 4 levels (FBXL4.11416.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 f-box/LRR-repeat protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802538 GCST90241136 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. F-box/LRR-repeat protein 4 levels (FBXL4.9951.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 f-box/LRR-repeat protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802538 GCST90241137 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. F-box/LRR-repeat protein 4 levels (FBXL4.9921.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 f-box/LRR-repeat protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802538 GCST90241138 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. F-box/LRR-repeat protein 5 levels (FBXL5.12846.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 f-box/LRR-repeat protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802539 GCST90241139 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. FACT complex subunit SSRP1 levels (SSRP1.5032.64.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fact complex subunit ssrp1 measurement http://www.ebi.ac.uk/efo/EFO_0020371 GCST90241140 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fas apoptotic inhibitory molecule 3 levels (FAIM3.6574.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fas apoptotic inhibitory molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0802540 GCST90241141 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. FAS-associated factor 2 levels (FAF2.6956.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fAS-associated factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0802541 GCST90241142 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. FAS-associated factor 2 levels (FAF2.9738.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fAS-associated factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0802541 GCST90241143 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fatty acid hydroxylase domain-containing protein 2 levels (FAXDC2.9074.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fatty acid hydroxylase domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802542 GCST90241144 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fatty acid-binding protein, adipocyte levels (FABP4.9851.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fatty acid-binding protein, adipocyte measurement http://www.ebi.ac.uk/efo/EFO_0010914 GCST90241145 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fatty acid-binding protein, epidermal levels (FABP5.4985.11.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fatty acid-binding protein, epidermal measurement http://www.ebi.ac.uk/efo/EFO_0020372 GCST90241146 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fatty acid-binding protein, heart levels (FABP3.4696.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fatty acid-binding protein, heart measurement http://www.ebi.ac.uk/efo/EFO_0020373 GCST90241147 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fatty acid-binding protein, liver levels (FABP1.11516.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fatty acid-binding protein, liver measurement http://www.ebi.ac.uk/efo/EFO_0021855 GCST90241148 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fatty-acid amide hydrolase 2 levels (FAAH2.8396.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fatty-acid amide hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802543 GCST90241149 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fc receptor-like protein 1 levels (FCRL1.5728.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Fc receptor-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801598 GCST90241150 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fc receptor-like protein 2 levels (FCRL2.7951.146.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Fc receptor-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802544 GCST90241151 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fc receptor-like protein 3 levels (FCRL3.4440.15.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Fc receptor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008127 GCST90241152 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fc receptor-like protein 4 levels (FCRL4.8973.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 Fc receptor-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801599 GCST90241153 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fc receptor-like protein 5 levels (FCRL5.6103.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Fc receptor-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802545 GCST90241154 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fc receptor-like protein 6 levels (FCRL6.6617.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 Fc receptor-like protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801600 GCST90241155 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Feline leukemia virus subgroup C receptor-related protein 1 levels (FLVCR1.9073.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 feline leukemia virus subgroup C receptor-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802546 GCST90241156 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ferritin levels (FTH1.FTL.3031.66.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90241157 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ferritin levels (FTH1.FTL.5934.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90241158 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fetal and adult testis-expressed transcript protein levels (FATE1.7740.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fetal and adult testis-expressed transcript protein measurement http://www.ebi.ac.uk/efo/EFO_0802547 GCST90241159 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibrinogen C domain-containing protein 1 levels (FIBCD1.9378.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibrinogen C domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802548 GCST90241160 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 1 levels (FGF1.3486.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020375 GCST90241161 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 10 levels (FGF10.2441.2.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020376 GCST90241162 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 16 levels (FGF16.13725.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90241163 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 16 levels (FGF16.4393.3.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90241164 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 19 levels (FGF19.2762.30.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90241165 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 20 levels (FGF20.2763.66.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 20 measurement http://www.ebi.ac.uk/efo/EFO_0020381 GCST90241166 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 23 levels (FGF23.3807.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90241167 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 4 levels (FGF4.4123.60.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020382 GCST90241168 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 5 levels (FGF5.3065.65.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90241169 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 6 levels (FGF6.4130.71.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020383 GCST90241170 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 7 levels (FGF7.14031.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90241171 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 7 levels (FGF7.4487.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90241172 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 8 isoform A levels (FGF8.4394.71.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 fibroblast growth factor 8 isoform A measurement http://www.ebi.ac.uk/efo/EFO_0020385 GCST90241173 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 8 isoform B levels (FGF8.2443.10.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 8 isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020386 GCST90241174 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor 9 levels (FGF9.2764.20.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020387 GCST90241175 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor receptor 2 levels (FGFR2.3808.76.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020389 GCST90241176 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor receptor 3 levels (FGFR3.13669.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90241177 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor receptor 3 levels (FGFR3.3809.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90241178 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibroblast growth factor receptor 4 levels (FGFR4.4988.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibroblast growth factor receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020391 GCST90241179 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibronectin levels (FN1.3435.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibronectin measurement http://www.ebi.ac.uk/efo/EFO_0008133 GCST90241180 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Fibronectin type III domain-containing protein 4 levels (FNDC4.13451.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 fibronectin type III domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802549 GCST90241181 Genome-wide genotyping array 2022-06-06 34906840 Trinder M 2021-12-06 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/34906840 Polygenic architecture and cardiovascular risk of familial combined hyperlipidemia. Familial combined hyperlipidemia defined by Brunzell criteria 3,838 British ancestry cases, 345,384 British ancestry controls NA Affymetrix [8802648] (imputed) 31 familial hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0001336 GCST90104003 Genome-wide genotyping array 2022-06-06 34906840 Trinder M 2021-12-06 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/34906840 Polygenic architecture and cardiovascular risk of familial combined hyperlipidemia. Familial combined hyperlipidemia defined by Goldstein criteria 1,688 British ancestry cases, 347,534 British ancestry controls NA Affymetrix [8802648] (imputed) 15 familial hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0001336 GCST90104004 Genome-wide genotyping array 2022-06-06 34906840 Trinder M 2021-12-06 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/34906840 Polygenic architecture and cardiovascular risk of familial combined hyperlipidemia. Familial combined hyperlipidemia defined by Dutch criteria 17,485 British ancestry cases, 331,737 British ancestry controls NA Affymetrix [8802648] (imputed) 69 familial hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0001336 GCST90104005 Genome-wide genotyping array 2022-06-06 34906840 Trinder M 2021-12-06 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/34906840 Polygenic architecture and cardiovascular risk of familial combined hyperlipidemia. Familial combined hyperlipidemia defined by Consensus criteria 39,961 British ancestry cases, 309,261 British ancestry controls NA Affymetrix [8802648] (imputed) 66 familial hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0001336 GCST90104006 Genome-wide genotyping array 2022-06-06 34906840 Trinder M 2021-12-06 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/34906840 Polygenic architecture and cardiovascular risk of familial combined hyperlipidemia. Familial combined hyperlipidemia defined by Mexico criteria 5,153 British ancestry cases, 344,069 British ancestry controls NA Affymetrix [8802648] (imputed) 48 familial hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0001336 GCST90104007 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 13 levels (CCL13.4144.13.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020195 GCST90240481 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 14 levels (CCL14.2900.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 C-C motif chemokine 14 measurement http://www.ebi.ac.uk/efo/EFO_0008042 GCST90240482 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 15 levels (CCL15.14109.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90240483 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 15 levels (CCL15.3509.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90240484 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 16 levels (CCL16.4913.78.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90240485 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 17 levels (CCL17.3519.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 C-C motif chemokine 17 measurement http://www.ebi.ac.uk/efo/EFO_0008045 GCST90240486 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 19 levels (CCL19.4922.13.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 C-C motif chemokine 19 measurement http://www.ebi.ac.uk/efo/EFO_0008047 GCST90240487 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 20 levels (CCL20.2468.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 20 measurement http://www.ebi.ac.uk/efo/EFO_0010910 GCST90240488 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 21 levels (CCL21.2516.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 C-C motif chemokine 21 measurement http://www.ebi.ac.uk/efo/EFO_0008048 GCST90240489 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 22 levels (CCL22.3508.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90240490 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 23 levels (CCL23.2913.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90240491 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 24 levels (CCL24.4128.27.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 24 measurement http://www.ebi.ac.uk/efo/EFO_0020197 GCST90240492 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 25 levels (CCL25.2705.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 8 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90240493 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 25 levels (CCL25.14068.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90240494 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 26 levels (CCL26.9168.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 26 measurement http://www.ebi.ac.uk/efo/EFO_0022024 GCST90240495 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial levels (PDK2.12651.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 [pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802230 GCST90240120 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 levels (PLCG1.4563.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 measurement http://www.ebi.ac.uk/efo/EFO_0020108 GCST90240121 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 14-3-3 protein epsilon levels (YWHAE.14157.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 14-3-3 protein epsilon measurement http://www.ebi.ac.uk/efo/EFO_0021958 GCST90240122 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 14-3-3 protein family levels (YWHAB.YWHAE.YWHAG.YWHAH.YWHAQ.YWHAZ.SFN.4707.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 14-3-3 protein family measurement http://www.ebi.ac.uk/efo/EFO_0020109 GCST90240123 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 14-3-3 protein sigma levels (SFN.4829.43.6) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 14-3-3 protein sigma measurement http://www.ebi.ac.uk/efo/EFO_0020110 GCST90240124 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 14-3-3 protein theta levels (YWHAQ.7625.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 14-3-3 protein theta measurement http://www.ebi.ac.uk/efo/EFO_0022011 GCST90240125 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 14-3-3 protein zeta/delta levels (YWHAZ.5858.6.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 14-3-3 protein zeta/delta measurement http://www.ebi.ac.uk/efo/EFO_0021996 GCST90240126 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 15-hydroxyprostaglandin dehydrogenase [NAD(+)] levels (HPGD.4995.16.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 15-hydroxyprostaglandin dehydrogenase [NAD(+)] measurement http://www.ebi.ac.uk/efo/EFO_0020111 GCST90240127 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 17-beta-hydroxysteroid dehydrogenase 14 levels (HSD17B14.13972.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 17-beta-hydroxysteroid dehydrogenase 14 measurement http://www.ebi.ac.uk/efo/EFO_0802231 GCST90240128 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 2-phosphoxylose phosphatase 1 levels (ACPL2.6079.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 2-phosphoxylose phosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803305 GCST90240129 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 2'-5'-oligoadenylate synthase 1 levels (OAS1.10361.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 2'-5'-oligoadenylate synthase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021911 GCST90240130 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 2',3'-cyclic-nucleotide 3'-phosphodiesterase levels (CNP.6609.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 2',3'-cyclic-nucleotide 3'-phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0802232 GCST90240131 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 26S proteasome non-ATPase regulatory subunit 1 levels (PSMD1.8824.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 26S proteasome non-ATPase regulatory subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0802233 GCST90240132 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 26S proteasome non-ATPase regulatory subunit 11 levels (PSMD11.13572.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 26S proteasome non-ATPase regulatory subunit 11 measurement http://www.ebi.ac.uk/efo/EFO_0802234 GCST90240133 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 26S proteasome non-ATPase regulatory subunit 4 levels (PSMD4.13568.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 26S proteasome non-ATPase regulatory subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0802235 GCST90240134 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 26S proteasome non-ATPase regulatory subunit 5 levels (PSMD5.10716.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 26S proteasome non-ATPase regulatory subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0801331 GCST90240135 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 26S proteasome non-ATPase regulatory subunit 7 levels (PSMD7.3898.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 26s proteasome non-atpase regulatory subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0020112 GCST90240136 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 3-hydroxy-3-methylglutaryl-coenzyme A reductase levels (HMGCR.5230.99.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 3-hydroxy-3-methylglutaryl-coenzymeAreductase measurement http://www.ebi.ac.uk/efo/EFO_0020113 GCST90240137 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 3-hydroxyacyl-CoA dehydrogenase type-2 levels (HSD17B10.4217.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 3-hydroxyacyl-coa dehydrogenase type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020114 GCST90240138 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 3-hydroxyanthranilate 3,4-dioxygenase levels (HAAO.5861.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 3-hydroxyanthranilate 3,4-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0021862 GCST90240139 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 3-mercaptopyruvate sulfurtransferase levels (MPST.12686.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 3-mercaptopyruvate sulfurtransferase measurement http://www.ebi.ac.uk/efo/EFO_0802236 GCST90240140 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 39S ribosomal protein L14, mitochondrial levels (MRPL14.8021.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 39S ribosomal protein L14, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802237 GCST90240141 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 39S ribosomal protein L14, mitochondrial levels (MRPL32.7982.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 39S ribosomal protein L14, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802237 GCST90240142 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 39S ribosomal protein L33, mitochondrial levels (MRPL33.13453.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 39S ribosomal protein L33, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801332 GCST90240143 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 39S ribosomal protein L34, mitochondrial levels (MRPL34.6933.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 39S ribosomal protein L34, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802238 GCST90240144 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 39S ribosomal protein L52, mitochondrial levels (MRPL52.7123.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 39S ribosomal protein L52, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802239 GCST90240145 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 4-hydroxy-2-oxoglutarate aldolase, mitochondrial levels (HOGA1.10024.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 4-hydroxy-2-oxoglutarate aldolase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802240 GCST90240146 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 40S ribosomal protein S3 levels (RPS3.5026.66.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 40s ribosomal protein S3 measurement http://www.ebi.ac.uk/efo/EFO_0020117 GCST90240147 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 40S ribosomal protein S3a levels (RPS3A.5484.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 40S ribosomal protein S3a measurement http://www.ebi.ac.uk/efo/EFO_0801333 GCST90240148 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 40S ribosomal protein S4, X isoform levels (RPS4X.9758.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 40S ribosomal protein S4, X isoform measurement http://www.ebi.ac.uk/efo/EFO_0801334 GCST90240149 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 40S ribosomal protein S7 levels (RPS7.3864.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 40s ribosomal protein S7 measurement http://www.ebi.ac.uk/efo/EFO_0020118 GCST90240150 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 40S ribosomal protein SA levels (RPSA.4957.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 40s ribosomal protein SA measurement http://www.ebi.ac.uk/efo/EFO_0020119 GCST90240151 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 5-formyltetrahydrofolate cyclo-ligase levels (MTHFS.14107.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 5-formyltetrahydrofolate cyclo-ligase measurement http://www.ebi.ac.uk/efo/EFO_0801335 GCST90240152 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 5'-Nucleotidase levels (NT5E.6993.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 5'-nucleotidase measurement http://www.ebi.ac.uk/efo/EFO_0802241 GCST90240153 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 5'(3')-deoxyribonucleotidase, cytosolic type levels (NT5C.12560.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 5'(3')-deoxyribonucleotidase, cytosolic type measurement http://www.ebi.ac.uk/efo/EFO_0801336 GCST90240154 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Argininosuccinate lyase levels (ASL.11241.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 argininosuccinate lyase measurement http://www.ebi.ac.uk/efo/EFO_0802287 GCST90240332 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Armadillo repeat-containing protein 5 levels (ARMC5.8785.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 armadillo repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802288 GCST90240333 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Armadillo repeat-containing protein 5 levels (ARMC5.8816.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 armadillo repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802288 GCST90240334 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Armadillo repeat-containing protein 5 levels (ARMC5.9945.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 armadillo repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802288 GCST90240335 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aromatic-L-amino-acid decarboxylase levels (DDC.3538.26.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 aromatic-l-amino-acid decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0020161 GCST90240336 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arrestin domain-containing protein 3 levels (ARRDC3.12352.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 arrestin domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802289 GCST90240337 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Artemin levels (ARTN.2939.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 artemin measurement http://www.ebi.ac.uk/efo/EFO_0020162 GCST90240338 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arylamine N-acetyltransferase 1 levels (NAT1.12632.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 arylamine N-acetyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801394 GCST90240339 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arylsulfatase A levels (ARSA.3583.54.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90240340 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arylsulfatase B levels (ARSB.3172.28.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 arylsulfatase B measurement http://www.ebi.ac.uk/efo/EFO_0008030 GCST90240341 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arylsulfatase K levels (ARSK.8269.327.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 arylsulfatase K measurement http://www.ebi.ac.uk/efo/EFO_0801395 GCST90240342 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Asialoglycoprotein receptor 1 levels (ASGR1.5452.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 asialoglycoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020164 GCST90240343 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Asialoglycoprotein receptor 2 levels (ASGR2.9474.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 asialoglycoprotein receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0802290 GCST90240344 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aspartate aminotransferase, cytoplasmic levels (GOT1.4912.17.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 aspartate aminotransferase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0008031 GCST90240345 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aspartyl/asparaginyl beta-hydroxylase levels (ASPH.6998.106.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 aspartyl/asparaginyl beta-hydroxylase measurement http://www.ebi.ac.uk/efo/EFO_0801396 GCST90240346 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Asporin levels (ASPN.6451.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 asporin measurement http://www.ebi.ac.uk/efo/EFO_0801397 GCST90240347 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Astacin-like metalloendopeptidase levels (ASTL.7993.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 astacin-like metalloendopeptidase measurement http://www.ebi.ac.uk/efo/EFO_0802291 GCST90240348 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. AT-rich interactive domain-containing protein 3A levels (ARID3A.3875.62.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 AT-rich interactive domain-containing protein 3A measurement http://www.ebi.ac.uk/efo/EFO_0020165 GCST90240349 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATP synthase subunit beta, mitochondrial levels (ATP5B.4965.27.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATP synthase subunit beta, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020166 GCST90240350 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATP-citrate synthase levels (ACLY.12700.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATP-citrate synthase measurement http://www.ebi.ac.uk/efo/EFO_0802292 GCST90240351 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 27 levels (CCL27.2192.63.10) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 27 measurement http://www.ebi.ac.uk/efo/EFO_0020198 GCST90240496 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 28 levels (CCL28.2890.59.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 C-C motif chemokine 28 measurement http://www.ebi.ac.uk/efo/EFO_0020199 GCST90240497 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 3 levels (CCL3.3040.59.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-C motif chemokine 3 measurement http://www.ebi.ac.uk/efo/EFO_0008051 GCST90240498 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 3-like 1 levels (CCL3L1.2783.18.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-C motif chemokine 3-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008052 GCST90240499 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 5 levels (CCL5.5480.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008053 GCST90240500 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macoilin levels (TMEM57.12367.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 macoilin measurement http://www.ebi.ac.uk/efo/EFO_0802722 GCST90241853 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macrophage colony-stimulating factor 1 levels (CSF1.3738.54.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 macrophage colony-stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020546 GCST90241854 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macrophage mannose receptor 1 levels (MRC1.2637.77.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 macrophage mannose receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020548 GCST90241855 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macrophage metalloelastase levels (MMP12.4496.60.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 macrophage metalloelastase measurement http://www.ebi.ac.uk/efo/EFO_0008220 GCST90241856 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macrophage migration inhibitory factor levels (MIF.5356.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST90241857 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macrophage scavenger receptor types I and II levels (MSR1.3684.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90241858 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macrophage scavenger receptor types I and II levels (MSR1.11207.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90241859 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Macrophage-stimulating protein receptor levels (MST1R.2640.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 macrophage-stimulating protein receptor measurement http://www.ebi.ac.uk/efo/EFO_0020550 GCST90241860 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Magnesium transporter NIPA4 levels (NIPAL4.12864.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 magnesium transporter NIPA4 measurement http://www.ebi.ac.uk/efo/EFO_0802723 GCST90241861 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAGUK p55 subfamily member 6 levels (MPP6.13490.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 MAGUK p55 subfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0801781 GCST90241862 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAGUK p55 subfamily member 7 levels (MPP7.12732.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MAGUK p55 subfamily member 7 measurement http://www.ebi.ac.uk/efo/EFO_0802724 GCST90241863 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Major prion protein levels (PRNP.6545.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 major prion protein measurement http://www.ebi.ac.uk/efo/EFO_0802725 GCST90241864 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Malate dehydrogenase, cytoplasmic levels (MDH1.3853.56.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 malate dehydrogenase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020551 GCST90241865 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Malectin levels (MLEC.6285.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 malectin measurement http://www.ebi.ac.uk/efo/EFO_0802726 GCST90241866 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Malignant T-cell-amplified sequence 1 levels (MCTS1.12488.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 malignant T-cell-amplified sequence 1 measurement http://www.ebi.ac.uk/efo/EFO_0801782 GCST90241867 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Malonyl-CoA decarboxylase, mitochondrial levels (MLYCD.11538.216.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 malonyl-CoA decarboxylase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802727 GCST90241868 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAM domain-containing protein 2 levels (MAMDC2.6119.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MAM domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802728 GCST90241869 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mammaglobin-B levels (SCGB2A1.5001.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mammaglobin-b measurement http://www.ebi.ac.uk/efo/EFO_0020552 GCST90241870 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mannan-binding lectin serine protease 1 levels (MASP1.3605.77.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90241871 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mannose-binding protein C levels (MBL2.3000.66.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 mannose-binding protein C measurement http://www.ebi.ac.uk/efo/EFO_0008224 GCST90241872 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mannosyl-oligosaccharide 1,2-alpha-mannosidase IA levels (MAN1A1.11291.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mannosyl-oligosaccharide 1,2-alpha-mannosidase IA measurement http://www.ebi.ac.uk/efo/EFO_0802729 GCST90241873 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mannosyl-oligosaccharide 1,2-alpha-mannosidase IB levels (MAN1A2.9077.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 mannosyl-oligosaccharide 1,2-alpha-mannosidase IB measurement http://www.ebi.ac.uk/efo/EFO_0801783 GCST90241874 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MANSC domain-containing protein 1 levels (MANSC1.9557.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 MANSC domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801784 GCST90241875 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MANSC domain-containing protein 4 levels (MANSC4.9578.263.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 MANSC domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801785 GCST90241876 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAP kinase-activated protein kinase 2 levels (MAPKAPK2.3820.68.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 MAP kinase-activated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008225 GCST90241877 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Megakaryocyte-associated tyrosine-protein kinase levels (MATK.3823.9.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 megakaryocyte-associated tyrosine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0020562 GCST90241903 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Melanocortin-2 receptor accessory protein levels (MRAP.7895.108.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 melanocortin-2 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0802734 GCST90241904 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Melanocortin-2 receptor accessory protein 2 levels (MRAP2.10889.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 melanocortin-2 receptor accessory protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802733 GCST90241905 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Melanocyte protein PMEL levels (PMEL.6472.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 melanocyte protein PMEL measurement http://www.ebi.ac.uk/efo/EFO_0801792 GCST90241906 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Melanoma-associated antigen 10 levels (MAGEA10.13610.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 melanoma-associated antigen 10 measurement http://www.ebi.ac.uk/efo/EFO_0801793 GCST90241907 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Melanoma-associated antigen 3 levels (MAGEA3.12576.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 melanoma-associated antigen 3 measurement http://www.ebi.ac.uk/efo/EFO_0801794 GCST90241908 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Melanoma-associated antigen B10 levels (MAGEB10.11456.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 melanoma-associated antigen B10 measurement http://www.ebi.ac.uk/efo/EFO_0802735 GCST90241909 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Melanoma-derived growth regulatory protein levels (MIA.2687.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90241910 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane magnesium transporter 1 levels (MMGT1.7225.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane magnesium transporter 1 measurement http://www.ebi.ac.uk/efo/EFO_0802736 GCST90241911 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane metallo-endopeptidase-like 1 levels (MMEL1.3627.71.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane metallo-endopeptidase-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020564 GCST90241912 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane protein FAM159B levels (FAM159B.10504.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane protein FAM159B measurement http://www.ebi.ac.uk/efo/EFO_0802737 GCST90241913 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane protein FAM174A levels (FAM174A.6597.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 membrane protein FAM174A measurement http://www.ebi.ac.uk/efo/EFO_0801795 GCST90241914 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane protein FAM174B levels (FAM174B.9054.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane protein FAM174B measurement http://www.ebi.ac.uk/efo/EFO_0802738 GCST90241915 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 levels (MAGI2.14066.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802739 GCST90241916 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane-associated progesterone receptor component 1 levels (PGRMC1.7863.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane-associated progesterone receptor component 1 measurement http://www.ebi.ac.uk/efo/EFO_0802740 GCST90241917 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane-associated progesterone receptor component 2 levels (PGRMC2.10631.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 membrane-associated progesterone receptor component 2 measurement http://www.ebi.ac.uk/efo/EFO_0801796 GCST90241918 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane-associated progesterone receptor component 2 levels (PGRMC2.10506.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane-associated progesterone receptor component 2 measurement http://www.ebi.ac.uk/efo/EFO_0801796 GCST90241919 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Membrane-associated progesterone receptor component 2 levels (PGRMC2.8681.93.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 membrane-associated progesterone receptor component 2 measurement http://www.ebi.ac.uk/efo/EFO_0801796 GCST90241920 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mesothelin levels (MSLN.3893.55.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mesothelin measurement http://www.ebi.ac.uk/efo/EFO_0020565 GCST90241921 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mesothelin levels (MSLN.3893.64.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mesothelin measurement http://www.ebi.ac.uk/efo/EFO_0020565 GCST90241922 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Metalloproteinase inhibitor 4 levels (TIMP4.6462.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 metalloproteinase inhibitor 4 measurement http://www.ebi.ac.uk/efo/EFO_0801797 GCST90241923 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Metallothionein-1F levels (MT1F.10416.79.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 metallothionein-1F measurement http://www.ebi.ac.uk/efo/EFO_0801798 GCST90241924 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Methionine-R-sulfoxide reductase B3 levels (MSRB3.7824.88.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 methionine-R-sulfoxide reductase B3 measurement http://www.ebi.ac.uk/efo/EFO_0802741 GCST90241925 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Methyl-CpG-binding domain protein 4 levels (MBD4.3891.56.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 methyl-cpg-binding domain protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020569 GCST90241926 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Methylmalonyl-CoA epimerase, mitochondrial levels (MCEE.9388.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 methylmalonyl-CoA epimerase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802742 GCST90241927 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAP kinase-activated protein kinase 3 levels (MAPKAPK3.3822.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90241878 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAP kinase-activated protein kinase 5 levels (MAPKAPK5.8382.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 MAP kinase-activated protein kinase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020553 GCST90241879 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAP kinase-activated protein kinase 5 levels (MAPKAPK5.3821.28.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MAP kinase-activated protein kinase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020553 GCST90241880 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Marginal zone B- and B1-cell-specific protein levels (PACAP.7780.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 marginal zone B- and B1-cell-specific protein measurement http://www.ebi.ac.uk/efo/EFO_0802730 GCST90241881 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Maspardin levels (SPG21.11122.97.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 maspardin measurement http://www.ebi.ac.uk/efo/EFO_0801786 GCST90241882 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mast cell-expressed membrane protein 1 levels (MCEMP1.6283.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 mast cell-expressed membrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801787 GCST90241883 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mast/stem cell growth factor receptor Kit levels (KIT.2475.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mast/stem cell growth factor receptor kit measurement http://www.ebi.ac.uk/efo/EFO_0020554 GCST90241884 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrilin-2 levels (MATN2.3325.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020555 GCST90241885 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrilin-3 levels (MATN3.3208.2.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020556 GCST90241886 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrilin-4 levels (MATN4.7083.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 matrilin-4 measurement http://www.ebi.ac.uk/efo/EFO_0801788 GCST90241887 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrilysin levels (MMP7.8475.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrilysin measurement http://www.ebi.ac.uk/efo/EFO_0008227 GCST90241888 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix extracellular phosphoglycoprotein levels (MEPE.3209.69.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrix extracellular phosphoglycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020557 GCST90241889 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix metalloproteinase-14 levels (MMP14.5002.76.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrix metalloproteinase-14 measurement http://www.ebi.ac.uk/efo/EFO_0020558 GCST90241890 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix metalloproteinase-16 levels (MMP16.9719.145.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrix metalloproteinase-16 measurement http://www.ebi.ac.uk/efo/EFO_0020559 GCST90241891 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix metalloproteinase-16 levels (MMP16.5268.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrix metalloproteinase-16 measurement http://www.ebi.ac.uk/efo/EFO_0020559 GCST90241892 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix metalloproteinase-17 levels (MMP17.2838.53.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrix metalloproteinase-17 measurement http://www.ebi.ac.uk/efo/EFO_0020560 GCST90241893 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix metalloproteinase-9 levels (MMP9.2579.17.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 matrix metalloproteinase-9 measurement http://www.ebi.ac.uk/efo/EFO_0020561 GCST90241894 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix-remodeling-associated protein 7 levels (MXRA7.8005.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 matrix-remodeling-associated protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0801789 GCST90241895 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix-remodeling-associated protein 8 levels (MXRA8.10521.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrix-remodeling-associated protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802731 GCST90241896 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Matrix-remodeling-associated protein 8 levels (MXRA8.7002.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 matrix-remodeling-associated protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802731 GCST90241897 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAX gene-associated protein levels (MGA.11587.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 MAX gene-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801790 GCST90241898 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. MAX-interacting protein 1 levels (MXI1.9035.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 MAX-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802732 GCST90241899 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mediator of RNA polymerase II transcription subunit 1 levels (MED1.5470.69.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90241900 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mediator of RNA polymerase II transcription subunit 1 levels (MED1.3892.21.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90241901 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Mediator of RNA polymerase II transcription subunit 4 levels (MED4.14021.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 mediator of RNA polymerase II transcription subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0801791 GCST90241902 Genome-wide genotyping array 2022-02-11 34210852 Akbari P 2021-07-01 Science www.ncbi.nlm.nih.gov/pubmed/34210852 Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity. Body mass index 549,780 European ancestry individuals, 95,846 admixed American ancestry individuals NA Illumina [NR] 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90094398 Exome-wide sequencing 2022-01-26 29155802 Huckins LM 2017-07-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29155802 Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Anorexia nervosa 2,158 European ancestry female cases, 15 ,485 European ancestry controls 1,299 European ancestry cases, 3,733 European ancestry controls Illumina [up to 524954] 5 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST012696 Exome genotyping array [Exome array] 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Roundabout homolog 3 levels (ROBO3.5117.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 roundabout homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0020714 GCST90242703 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. rRNA methyltransferase 3, mitochondrial levels (RNMTL1.9584.105.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 rRNA methyltransferase 3, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802033 GCST90242704 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RUN and FYVE domain-containing protein 1 levels (RUFY1.11425.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RUN and FYVE domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803040 GCST90242705 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Runt-related transcription factor 3 levels (RUNX3.11138.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 runt-related transcription factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802034 GCST90242706 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. S-formylglutathione hydrolase levels (ESD.4984.83.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 S-formylglutathione hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0008275 GCST90242707 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. S-methyl-5'-thioadenosine phosphorylase levels (MTAP.9910.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 s-methyl-5'-thioadenosine phosphorylase measurement http://www.ebi.ac.uk/efo/EFO_0803041 GCST90242708 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. S-phase kinase-associated protein 1 levels (SKP1.3902.21.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 s-phase kinase-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020715 GCST90242709 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SAGA-associated factor 29 homolog levels (CCDC101.12788.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SAGA-associated factor 29 homolog measurement http://www.ebi.ac.uk/efo/EFO_0803042 GCST90242710 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Salivary acidic proline-rich phosphoprotein 1/2 levels (PRH1.10502.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 salivary acidic proline-rich phosphoprotein 1/2 measurement http://www.ebi.ac.uk/efo/EFO_0802035 GCST90242711 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sarcoplasmic/endoplasmic reticulum calcium ATPase 3 levels (ATP2A3.13510.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sarcoplasmic/endoplasmic reticulum calcium ATPase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802036 GCST90242712 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SAYSvFN domain-containing protein 1 levels (SAYSD1.6594.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 SAYSvFN domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803043 GCST90242713 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class A member 3 levels (SCARA3.11292.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 scavenger receptor class A member 3 measurement http://www.ebi.ac.uk/efo/EFO_0803044 GCST90242714 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class A member 3 levels (SCARA3.9731.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 scavenger receptor class A member 3 measurement http://www.ebi.ac.uk/efo/EFO_0803044 GCST90242715 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class A member 3 levels (SCARA3.10872.103.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 scavenger receptor class A member 3 measurement http://www.ebi.ac.uk/efo/EFO_0803044 GCST90242716 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class A member 3 levels (SCARA3.9569.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 scavenger receptor class A member 3 measurement http://www.ebi.ac.uk/efo/EFO_0803044 GCST90242717 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class A member 5 levels (SCARA5.10419.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 scavenger receptor class A member 5 measurement http://www.ebi.ac.uk/efo/EFO_0802037 GCST90242718 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class F member 2 levels (SCARF2.8956.96.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90242719 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor class F member 2 levels (SCARF2.5130.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90242720 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Scavenger receptor cysteine-rich type 1 protein M130 levels (CD163.5028.59.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 scavenger receptor cysteine-rich type 1 protein m130 measurement http://www.ebi.ac.uk/efo/EFO_0020717 GCST90242721 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sclerostin levels (SOST.13101.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sclerostin measurement http://www.ebi.ac.uk/efo/EFO_0010606 GCST90242722 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SCP2 sterol-binding domain-containing protein 1 levels (SCP2D1.14175.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 SCP2 sterol-binding domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802038 GCST90242723 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretagogin levels (SCGN.10894.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 secretagogin measurement http://www.ebi.ac.uk/efo/EFO_0803045 GCST90242724 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secreted and transmembrane protein 1 levels (SECTM1.13093.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 secreted and transmembrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021852 GCST90242725 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secreted frizzled-related protein 1 levels (SFRP1.3221.54.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 secreted frizzled-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020718 GCST90242726 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secreted frizzled-related protein 2 levels (SFRP2.7751.121.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 secreted frizzled-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802039 GCST90242727 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ELAV-like protein 1 levels (ELAVL1.11592.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ELAV-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801562 GCST90241032 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Electroneutral sodium bicarbonate exchanger 1 levels (SLC4A8.12798.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 electroneutral sodium bicarbonate exchanger 1 measurement http://www.ebi.ac.uk/efo/EFO_0802520 GCST90241033 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Elongation factor 1-beta levels (EEF1B2.5882.34.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 elongation factor 1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020345 GCST90241034 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EMI domain-containing protein 1 levels (EMID1.13021.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 EMI domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802521 GCST90241035 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EMILIN-3 levels (EMILIN3.8773.172.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 EMILIN-3 measurement http://www.ebi.ac.uk/efo/EFO_0801563 GCST90241036 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EMILIN-3 levels (EMILIN3.8964.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 EMILIN-3 measurement http://www.ebi.ac.uk/efo/EFO_0801563 GCST90241037 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EMILIN-3 levels (EMILIN3.9991.112.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 EMILIN-3 measurement http://www.ebi.ac.uk/efo/EFO_0801563 GCST90241038 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ena/VASP-like protein levels (EVL.11656.110.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Ena/VASP-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801564 GCST90241039 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endogenous retrovirus group V member 1 Env polyprotein levels (ERVV.1.12531.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 endogenous retrovirus group V member 1 Env polyprotein measurement http://www.ebi.ac.uk/efo/EFO_0801565 GCST90241040 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoglin levels (ENG.4908.6.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 endoglin measurement http://www.ebi.ac.uk/efo/EFO_0008118 GCST90241041 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoplasmic reticulum aminopeptidase 1 levels (ERAP1.4964.67.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90241042 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoplasmic reticulum aminopeptidase 2 levels (ERAP2.8960.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 endoplasmic reticulum aminopeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801566 GCST90241043 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoplasmic reticulum lectin 1 levels (ERLEC1.8957.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 endoplasmic reticulum lectin 1 measurement http://www.ebi.ac.uk/efo/EFO_0801567 GCST90241044 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase levels (MAN1B1.7071.23.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801568 GCST90241045 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoplasmic reticulum resident protein 29 levels (ERP29.13728.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 endoplasmic reticulum resident protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0020346 GCST90241046 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoplasmic reticulum resident protein 44 levels (ERP44.6064.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 endoplasmic reticulum resident protein 44 measurement http://www.ebi.ac.uk/efo/EFO_0801569 GCST90241047 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endoplasmin levels (HSP90B1.6393.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 endoplasmin measurement http://www.ebi.ac.uk/efo/EFO_0801570 GCST90241048 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endostatin levels (COL18A1.2201.17.6) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 endostatin measurement http://www.ebi.ac.uk/efo/EFO_0020347 GCST90241049 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelial cell-selective adhesion molecule levels (ESAM.7841.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90241050 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelial cell-selective adhesion molecule levels (ESAM.2981.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90241051 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelial cell-specific molecule 1 levels (ESM1.3805.16.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 endothelial cell-specific molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010912 GCST90241052 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelial differentiation-related factor 1 levels (EDF1.12415.122.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 endothelial differentiation-related factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801571 GCST90241053 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelial monocyte-activating polypeptide 2 levels (AIMP1.2714.78.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 endothelial monocyte-activating polypeptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020348 GCST90241054 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelin-2 levels (EDN2.12574.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 endothelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801572 GCST90241055 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelin-converting enzyme 1 levels (ECE1.3611.70.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90241056 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secreted frizzled-related protein 3 levels (FRZB.13740.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90242728 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secreted frizzled-related protein 3 levels (FRZB.2841.13.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90242729 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secreted Ly-6/uPAR-related protein 1 levels (SLURP1.6401.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 secreted Ly-6/uPAR-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802040 GCST90242730 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretoglobin family 1C member 1 levels (SCGB1C1.5960.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 secretoglobin family 1C member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802041 GCST90242731 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretoglobin family 1D member 2 levels (SCGB1D2.6508.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 secretoglobin family 1D member 2 measurement http://www.ebi.ac.uk/efo/EFO_0803046 GCST90242732 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretogranin-1 levels (CHGB.8235.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 secretogranin-1 measurement http://www.ebi.ac.uk/efo/EFO_0803047 GCST90242733 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretogranin-2 levels (SCG2.8377.87.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 secretogranin-2 measurement http://www.ebi.ac.uk/efo/EFO_0803048 GCST90242734 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretogranin-3 levels (SCG3.7957.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 secretogranin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802042 GCST90242735 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretory carrier-associated membrane protein 5 levels (SCAMP5.13509.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 secretory carrier-associated membrane protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803049 GCST90242736 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Secretory phospholipase A2 receptor levels (PLA2R1.10916.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 secretory phospholipase A2 receptor measurement http://www.ebi.ac.uk/efo/EFO_0802043 GCST90242737 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Segment polarity protein dishevelled homolog DVL-2 levels (DVL2.13575.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 segment polarity protein dishevelled homolog DVL-2 measurement http://www.ebi.ac.uk/efo/EFO_0802044 GCST90242738 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Seizure 6-like protein 2 levels (SEZ6L2.3867.49.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 seizure 6-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020720 GCST90242739 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Selenide, water dikinase 1 levels (SEPHS1.14083.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 selenide, water dikinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802045 GCST90242740 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Selenoprotein S levels (VIMP.11286.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 selenoprotein S measurement http://www.ebi.ac.uk/efo/EFO_0802046 GCST90242741 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-3A levels (SEMA3A.3222.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90242742 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-3B levels (SEMA3B.5667.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 semaphorin-3B measurement http://www.ebi.ac.uk/efo/EFO_0802047 GCST90242743 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-3C levels (SEMA3C.6448.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 semaphorin-3C measurement http://www.ebi.ac.uk/efo/EFO_0802048 GCST90242744 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-3E levels (SEMA3E.5363.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90242745 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-3G levels (SEMA3G.5628.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 semaphorin-3G measurement http://www.ebi.ac.uk/efo/EFO_0802049 GCST90242746 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-4C levels (SEMA4C.7923.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 semaphorin-4C measurement http://www.ebi.ac.uk/efo/EFO_0803050 GCST90242747 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-4D levels (SEMA4D.5737.61.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 semaphorin-4D measurement http://www.ebi.ac.uk/efo/EFO_0802050 GCST90242748 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-5A levels (SEMA5A.13132.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 semaphorin-5A measurement http://www.ebi.ac.uk/efo/EFO_0021864 GCST90242749 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-6A levels (SEMA6A.7945.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90242750 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-6A levels (SEMA6A.5122.92.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90242751 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-6C levels (SEMA6C.14597.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 semaphorin-6C measurement http://www.ebi.ac.uk/efo/EFO_0803051 GCST90242752 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RNF34 levels (RNF34.13386.248.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase RNF34 measurement http://www.ebi.ac.uk/efo/EFO_0802512 GCST90241007 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RNF43 levels (RNF43.14120.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 e3 ubiquitin-protein ligase RNF43 measurement http://www.ebi.ac.uk/efo/EFO_0021886 GCST90241008 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RNF8 levels (RNF8.14663.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 E3 ubiquitin-protein ligase RNF8 measurement http://www.ebi.ac.uk/efo/EFO_0801557 GCST90241009 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase ZFP91 levels (ZFP91.13651.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase ZFP91 measurement http://www.ebi.ac.uk/efo/EFO_0802513 GCST90241010 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase ZNRF3 levels (ZNRF3.13428.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase ZNRF3 measurement http://www.ebi.ac.uk/efo/EFO_0021943 GCST90241011 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase ZNRF3 levels (ZNRF3.14122.132.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase ZNRF3 measurement http://www.ebi.ac.uk/efo/EFO_0021943 GCST90241012 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Early endosome antigen 1 levels (EEA1.14043.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 early endosome antigen 1 measurement http://www.ebi.ac.uk/efo/EFO_0802514 GCST90241013 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Early placenta insulin-like peptide levels (INSL4.6410.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 early placenta insulin-like peptide measurement http://www.ebi.ac.uk/efo/EFO_0802515 GCST90241014 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ecto-ADP-ribosyltransferase 3 levels (ART3.10970.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 ecto-ADP-ribosyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801558 GCST90241015 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ecto-ADP-ribosyltransferase 3 levels (ART3.7970.315.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ecto-ADP-ribosyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801558 GCST90241016 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ecto-ADP-ribosyltransferase 4 levels (ART4.6576.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ecto-ADP-ribosyltransferase 4 measurement http://www.ebi.ac.uk/efo/EFO_0801559 GCST90241017 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ecto-NOX disulfide-thiol exchanger 2 levels (ENOX2.13422.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ecto-NOX disulfide-thiol exchanger 2 measurement http://www.ebi.ac.uk/efo/EFO_0802516 GCST90241018 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectodysplasin-A, secreted form levels (EDA.14024.196.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ectodysplasin-a, secreted form measurement http://www.ebi.ac.uk/efo/EFO_0020341 GCST90241019 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectodysplasin-A, secreted form levels (EDA.2826.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ectodysplasin-a, secreted form measurement http://www.ebi.ac.uk/efo/EFO_0020341 GCST90241020 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 1 levels (ENTPD1.7999.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90241021 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 1 levels (ENTPD1.3182.38.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90241022 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 3 levels (ENTPD3.4436.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ectonucleoside triphosphate diphosphohydrolase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020343 GCST90241023 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 5 levels (ENTPD5.4437.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90241024 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 6 levels (ENTPD6.8932.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ectonucleoside triphosphate diphosphohydrolase 6 measurement http://www.ebi.ac.uk/efo/EFO_0802517 GCST90241025 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectonucleotide pyrophosphatase/phosphodiesterase family member 5 levels (ENPP5.6556.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ectonucleotide pyrophosphatase/phosphodiesterase family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801560 GCST90241026 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels (ENPP7.4435.66.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0020344 GCST90241027 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EF-hand calcium-binding domain-containing protein 14 levels (EFCAB14.10830.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 EF-hand calcium-binding domain-containing protein 14 measurement http://www.ebi.ac.uk/efo/EFO_0802518 GCST90241028 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EH domain-binding protein 1 levels (EHBP1.12813.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 EH domain-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801561 GCST90241029 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EH domain-containing protein 4 levels (EHD4.11421.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 EH domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802519 GCST90241030 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Elafin levels (PI3.4982.54.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90241031 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Endothelin-converting enzyme 1 levels (ECE1.8767.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90241057 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Engulfment and cell motility protein 1 levels (ELMO1.12764.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 engulfment and cell motility protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802522 GCST90241058 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Enhancer of mRNA-decapping protein 4 levels (EDC4.13066.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 enhancer of mRNA-decapping protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802523 GCST90241059 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Enhancer of rudimentary homolog levels (ERH.11614.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 enhancer of rudimentary homolog measurement http://www.ebi.ac.uk/efo/EFO_0801573 GCST90241060 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Enteropeptidase levels (TMPRSS15.3189.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 enteropeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020349 GCST90241061 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Envoplakin levels (EVPL.14019.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 envoplakin measurement http://www.ebi.ac.uk/efo/EFO_0802524 GCST90241062 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Eotaxin levels (CCL11.5301.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90241063 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. EP300-interacting inhibitor of differentiation 3 levels (EID3.8079.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 EP300-interacting inhibitor of differentiation 3 measurement http://www.ebi.ac.uk/efo/EFO_0802525 GCST90241064 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-A receptor 1 levels (EPHA1.3431.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ephrin type-A receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008123 GCST90241065 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-A receptor 10 levels (EPHA10.6036.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin type-a receptor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020350 GCST90241066 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-A receptor 2 levels (EPHA2.4834.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin type-a receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020351 GCST90241067 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-A receptor 5 levels (EPHA5.14089.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ephrin type-a receptor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020353 GCST90241068 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-A receptor 5 levels (EPHA5.3806.55.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin type-a receptor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020353 GCST90241069 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-B receptor 2 levels (EPHB2.8225.86.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90241070 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-B receptor 2 levels (EPHB2.5077.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90241071 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-B receptor 2 levels (EPHB2.8348.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90241072 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-B receptor 3 levels (EPHB3.9220.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ephrin type-B receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0801574 GCST90241073 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-B receptor 4 levels (EPHB4.3612.6.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin type-b receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020354 GCST90241074 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-B receptor 6 levels (EPHB6.5078.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90241075 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin type-B receptor 6 levels (EPHB6.9261.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90241076 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-A2 levels (EFNA2.14124.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-A2 measurement http://www.ebi.ac.uk/efo/EFO_0021944 GCST90241077 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-A3 levels (EFNA3.14153.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-A3 measurement http://www.ebi.ac.uk/efo/EFO_0021956 GCST90241078 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-A3 levels (EFNA3.5759.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-A3 measurement http://www.ebi.ac.uk/efo/EFO_0021956 GCST90241079 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-A4 levels (EFNA4.2614.28.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-A4 measurement http://www.ebi.ac.uk/efo/EFO_0020356 GCST90241080 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ephrin-A5 levels (EFNA5.2615.60.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ephrin-A5 measurement http://www.ebi.ac.uk/efo/EFO_0020357 GCST90241081 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semaphorin-7A levels (SEMA7A.7019.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 semaphorin-7A measurement http://www.ebi.ac.uk/efo/EFO_0803052 GCST90242753 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semenogelin-1 levels (SEMG1.7115.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 semenogelin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802051 GCST90242754 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Semenogelin-2 levels (SEMG2.6373.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 semenogelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802052 GCST90242755 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sentrin-specific protease 7 levels (SENP7.12626.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sentrin-specific protease 7 measurement http://www.ebi.ac.uk/efo/EFO_0803053 GCST90242756 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sepiapterin reductase levels (SPR.9287.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sepiapterin reductase measurement http://www.ebi.ac.uk/efo/EFO_0803054 GCST90242757 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Septin-10 levels (SEPT10.12690.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 septin-10 measurement http://www.ebi.ac.uk/efo/EFO_0802053 GCST90242758 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine palmitoyltransferase 1 levels (SPTLC1.7886.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine palmitoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803055 GCST90242759 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Serine palmitoyltransferase 2 levels (SPTLC2.7267.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 serine palmitoyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0803056 GCST90242760 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ISG15--protein ligase HERC5 levels (HERC5.12934.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ISG15--protein ligase HERC5 measurement http://www.ebi.ac.uk/efo/EFO_0802501 GCST90240990 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase CBL levels (CBL.12016.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 E3 ubiquitin-protein ligase CBL measurement http://www.ebi.ac.uk/efo/EFO_0801552 GCST90240991 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase CCNB1IP1 levels (CCNB1IP1.9728.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase CCNB1IP1 measurement http://www.ebi.ac.uk/efo/EFO_0802502 GCST90240992 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase DTX1 levels (DTX1.11430.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase DTX1 measurement http://www.ebi.ac.uk/efo/EFO_0802503 GCST90240993 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase DTX3L levels (DTX3L.11643.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 E3 ubiquitin-protein ligase DTX3L measurement http://www.ebi.ac.uk/efo/EFO_0801553 GCST90240994 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase FANCL levels (FANCL.10063.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase FANCL measurement http://www.ebi.ac.uk/efo/EFO_0802504 GCST90240995 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase HECW1 levels (HECW1.12669.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase HECW1 measurement http://www.ebi.ac.uk/efo/EFO_0802505 GCST90240996 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase Mdm2 levels (MDM2.4245.80.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 e3 ubiquitin-protein ligase mdm2 measurement http://www.ebi.ac.uk/efo/EFO_0020340 GCST90240997 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase NEURL1 levels (NEURL1.13604.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 E3 ubiquitin-protein ligase NEURL1 measurement http://www.ebi.ac.uk/efo/EFO_0801554 GCST90240998 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase parkin levels (PARK2.13013.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 e3 ubiquitin-protein ligase parkin measurement http://www.ebi.ac.uk/efo/EFO_0802506 GCST90240999 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase pellino homolog 2 levels (PELI2.12702.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 e3 ubiquitin-protein ligase pellino homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0802507 GCST90241000 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RBBP6 levels (RBBP6.9887.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase RBBP6 measurement http://www.ebi.ac.uk/efo/EFO_0802508 GCST90241001 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase rififylin levels (RFFL.14186.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 e3 ubiquitin-protein ligase rififylin measurement http://www.ebi.ac.uk/efo/EFO_0802509 GCST90241002 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RNF114 levels (RNF114.9957.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase RNF114 measurement http://www.ebi.ac.uk/efo/EFO_0802510 GCST90241003 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RNF128 levels (RNF128.6510.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 E3 ubiquitin-protein ligase RNF128 measurement http://www.ebi.ac.uk/efo/EFO_0801555 GCST90241004 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RNF13 levels (RNF13.8087.250.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 E3 ubiquitin-protein ligase RNF13 measurement http://www.ebi.ac.uk/efo/EFO_0801556 GCST90241005 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E3 ubiquitin-protein ligase RNF149 levels (RNF149.9773.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 E3 ubiquitin-protein ligase RNF149 measurement http://www.ebi.ac.uk/efo/EFO_0802511 GCST90241006 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Detectable estradiol levels 48,487 European ancestry cases, 181,479 European ancestry controls NA NR [NR] (imputed) 10 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104271 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Testosterone levels 182,648 European ancestry individuals NA NR [NR] (imputed) 157 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90104272 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Sex hormone-binding globulin levels 196,901 European ancestry individuals NA NR [NR] (imputed) 284 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90104273 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Estradiol levels in postmenopausal women 3,759 European ancestry individuals NA NR [NR] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104274 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Detectable estradiol levels in postmenopausal women 3,759 European ancestry cases, 80,435 European ancestry controls NA NR [NR] (imputed) 7 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104275 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Testosterone levels in postmenopausal women 84,003 European ancestry individuals NA NR [NR] (imputed) 61 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90104276 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Sex hormone-binding globulin levels in postmenopausal women 92,911 European ancestry individuals NA NR [NR] (imputed) 169 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90104277 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Estradiol levels in premenopausal women 33,032 European ancestry individuals NA NR [NR] (imputed) 1 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104278 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Detectable estradiol levels in premenopausal women 33,032 European ancestry cases, 18,049 European ancestry controls NA NR [NR] (imputed) 6 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104279 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Testosterone levels in premenopausal women 44,401 European ancestry individuals NA NR [NR] (imputed) 40 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90104280 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Sex hormone-binding globulin levels in premenopausal women 43,477 European ancestry individuals NA NR [NR] (imputed) 49 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90104281 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Estradiol levels 1,706 African ancestry individuals NA NR [NR] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104282 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Detectable estradiol levels 1,706 African ancestry cases, 3,630 African ancestry controls NA NR [NR] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104283 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Testosterone levels 4,229 African ancestry individuals NA NR [NR] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90104284 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Sex hormone-binding globulin levels 4,522 African ancestry individuals NA NR [NR] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90104285 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Estradiol levels in postmenopausal women 76 African ancestry individuals NA NR [NR] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104286 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Detectable estradiol levels in postmenopausal women 76 African ancestry cases, 1,124 African ancestry controls NA NR [NR] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104287 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Testosterone levels in postmenopausal women 1,196 African ancestry individuals NA NR [NR] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90104288 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Sex hormone-binding globulin levels in postmenopausal women 1,319 African ancestry individuals NA NR [NR] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90104289 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Estradiol levels in premenopausal women 1,285 African ancestry individuals NA NR [NR] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104290 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Detectable estradiol levels in premenopausal women 1,285 African ancestry cases, 709 African ancestry controls NA NR [NR] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104291 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Testosterone levels in premenopausal women 1,639 African ancestry individuals NA NR [NR] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90104292 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Sex hormone-binding globulin levels in premenopausal women 1,697 African ancestry individuals NA NR [NR] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90104293 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Estradiol levels 1,706 African ancestry individuals, 48,487 European ancestry individuals NA NR [NR] (imputed) 1 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104294 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Estradiol levels 48,487 European ancestry individuals NA NR [NR] (imputed) 1 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104270 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bone morphogenetic protein 6 levels (BMP6.8459.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90240457 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bone morphogenetic protein receptor type-1A levels (BMPR1A.4859.6.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bone morphogenetic protein receptor type-1a measurement http://www.ebi.ac.uk/efo/EFO_0020188 GCST90240460 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bone sialoprotein 2 levels (IBSP.14023.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 bone sialoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020190 GCST90240461 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bone sialoprotein 2 levels (IBSP.3415.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bone sialoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020190 GCST90240462 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BPI fold-containing family A member 1 levels (BPIFA1.6473.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BPI fold-containing family A member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802336 GCST90240463 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bone morphogenetic protein 10 levels (BMP10.3587.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bone morphogenetic protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020185 GCST90240456 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bone morphogenetic protein 6 levels (BMP6.3736.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90240458 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bone morphogenetic protein 7 levels (BMP7.2972.57.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 bone morphogenetic protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020187 GCST90240459 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BPI fold-containing family B member 1 levels (BPIFB1.11246.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 BPI fold-containing family B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0801429 GCST90240464 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Brain natriuretic peptide 32 levels (NPPB.3723.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 brain natriuretic peptide 32 measurement http://www.ebi.ac.uk/efo/EFO_0020191 GCST90240465 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Brain-derived neurotrophic factor levels (BDNF.2421.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST90240466 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Brain-specific serine protease 4 levels (PRSS22.4534.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 brain-specific serine protease 4 measurement http://www.ebi.ac.uk/efo/EFO_0020192 GCST90240467 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BRCA1-associated RING domain protein 1 levels (BARD1.13977.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BRCA1-associated RING domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802337 GCST90240468 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Breast cancer anti-estrogen resistance protein 3 levels (BCAR3.12634.79.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 breast cancer anti-estrogen resistance protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008040 GCST90240469 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Brevican core protein levels (BCAN.3461.58.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 brevican core protein measurement http://www.ebi.ac.uk/efo/EFO_0020193 GCST90240470 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BRICHOS domain-containing protein 5 levels (BRICD5.6612.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 BRICHOS domain-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801430 GCST90240471 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BRISC complex subunit Abro1 levels (FAM175B.8945.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BRISC complex subunit Abro1 measurement http://www.ebi.ac.uk/efo/EFO_0802338 GCST90240472 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bromodomain testis-specific protein levels (BRDT.12748.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 bromodomain testis-specific protein measurement http://www.ebi.ac.uk/efo/EFO_0802339 GCST90240473 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bromodomain-containing protein 1 levels (BRD1.11607.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 bromodomain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801431 GCST90240474 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Brorin levels (VWC2.11121.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 brorin measurement http://www.ebi.ac.uk/efo/EFO_0801432 GCST90240475 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Brother of CDO levels (BOC.4328.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 brother of CDO measurement http://www.ebi.ac.uk/efo/EFO_0020194 GCST90240476 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BTB/POZ domain-containing protein KCTD5 levels (KCTD5.12473.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BTB/POZ domain-containing protein KCTD5 measurement http://www.ebi.ac.uk/efo/EFO_0802340 GCST90240477 Genome-wide genotyping array 2022-01-14 33430342 Younes N 2021-01-07 J Pers Med www.ncbi.nlm.nih.gov/pubmed/33430342 A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank Cohort. Total body bone mineral density 3,000 Qatari ancestry individuals NA Illumina [1084750] 13 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90093097 Genome-wide sequencing 2022-01-14 33430342 Younes N 2021-01-07 J Pers Med www.ncbi.nlm.nih.gov/pubmed/33430342 A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank Cohort. Bone mineral density (spine) 3,000 Qatari ancestry individuals NA Illumina [1084750] 1 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90093098 Genome-wide sequencing 2022-01-14 33430342 Younes N 2021-01-07 J Pers Med www.ncbi.nlm.nih.gov/pubmed/33430342 A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank Cohort. Bone mineral density (pelvis) 3,000 Qatari ancestry individuals NA Illumina [1084750] 1 pelvis bone mineral density http://www.ebi.ac.uk/efo/EFO_0020104 GCST90093099 Genome-wide sequencing 2022-01-14 33430342 Younes N 2021-01-07 J Pers Med www.ncbi.nlm.nih.gov/pubmed/33430342 A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank Cohort. Bone mineral density (trunk) 3,000 Qatari ancestry individuals NA Illumina [1084750] 3 trunk bone mineral density http://www.ebi.ac.uk/efo/EFO_0020105 GCST90093100 Genome-wide sequencing 2022-01-14 33430342 Younes N 2021-01-07 J Pers Med www.ncbi.nlm.nih.gov/pubmed/33430342 A Whole-Genome Sequencing Association Study of Low Bone Mineral Density Identifies New Susceptibility Loci in the Phase I Qatar Biobank Cohort. Bone mineral density (Ward's triangle area) 3,000 Qatari ancestry individuals NA Illumina [1084750] 1 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90093101 Genome-wide sequencing 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Butyrophilin-like protein 9 levels (BTNL9.7950.142.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 butyrophilin-like protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0802341 GCST90240478 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 1 levels (CCL1.2770.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 1 measurement http://www.ebi.ac.uk/efo/EFO_0008041 GCST90240479 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 1 levels (CCL1.13687.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-C motif chemokine 1 measurement http://www.ebi.ac.uk/efo/EFO_0008041 GCST90240480 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily C member 18 levels (DNAJC18.8033.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily C member 18 measurement http://www.ebi.ac.uk/efo/EFO_0802490 GCST90240959 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily C member 27 levels (DNAJC27.12799.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily C member 27 measurement http://www.ebi.ac.uk/efo/EFO_0802491 GCST90240960 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily C member 30 levels (DNAJC30.7866.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 DnaJ homolog subfamily C member 30 measurement http://www.ebi.ac.uk/efo/EFO_0801542 GCST90240961 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily C member 4 levels (DNAJC4.8016.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily C member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802492 GCST90240962 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Docking protein 2 levels (DOK2.14246.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 docking protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801543 GCST90240963 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1 levels (RPN1.6458.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0801544 GCST90240964 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1 levels (RPN1.10490.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0801544 GCST90240965 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dorsal root ganglia homeobox protein levels (DRGX.8034.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 dorsal root ganglia homeobox protein measurement http://www.ebi.ac.uk/efo/EFO_0801545 GCST90240966 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Double-strand break repair protein MRE11A levels (MRE11A.11319.106.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 double-strand break repair protein MRE11A measurement http://www.ebi.ac.uk/efo/EFO_0802493 GCST90240967 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Double-stranded RNA-binding protein Staufen homolog 1 levels (STAU1.12471.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 double-stranded RNA-binding protein Staufen homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0801546 GCST90240968 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Double-stranded RNA-binding protein Staufen homolog 2 levels (STAU2.12970.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 double-stranded RNA-binding protein Staufen homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0801547 GCST90240969 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Down syndrome cell adhesion molecule levels (DSCAM.9175.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 down syndrome cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0022028 GCST90240970 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Drebrin-like protein levels (DBNL.4978.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 drebrin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020333 GCST90240971 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity mitogen-activated protein kinase kinase 1 levels (MAP2K1.2864.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 dual specificity mitogen-activated protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020335 GCST90240972 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity mitogen-activated protein kinase kinase 3 levels (MAP2K3.6151.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 dual specificity mitogen-activated protein kinase kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0022005 GCST90240973 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity mitogen-activated protein kinase kinase 4 levels (MAP2K4.5242.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 dual specificity mitogen-activated protein kinase kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0008113 GCST90240974 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity protein kinase CLK2 levels (CLK2.11327.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dual specificity protein kinase CLK2 measurement http://www.ebi.ac.uk/efo/EFO_0801548 GCST90240975 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity protein phosphatase 13 isoform A levels (DUSP13.6525.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dual specificity protein phosphatase 13 isoform A measurement http://www.ebi.ac.uk/efo/EFO_0801549 GCST90240976 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity protein phosphatase 15 levels (DUSP15.12838.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dual specificity protein phosphatase 15 measurement http://www.ebi.ac.uk/efo/EFO_0802494 GCST90240977 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity protein phosphatase 16 levels (DUSP16.14631.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dual specificity protein phosphatase 16 measurement http://www.ebi.ac.uk/efo/EFO_0802495 GCST90240978 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity protein phosphatase 4 levels (DUSP4.10035.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 dual specificity protein phosphatase 4 measurement http://www.ebi.ac.uk/efo/EFO_0801550 GCST90240979 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity protein phosphatase 6 levels (DUSP6.12341.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dual specificity protein phosphatase 6 measurement http://www.ebi.ac.uk/efo/EFO_0802496 GCST90240980 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dual specificity tyrosine-phosphorylation-regulated kinase 3 levels (DYRK3.4359.87.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dual specificity tyrosine-phosphorylation-regulated kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020337 GCST90240981 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dynactin subunit 2 levels (DCTN2.5879.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dynactin subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0020338 GCST90240982 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dynactin-associated protein levels (DYNAP.10692.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dynactin-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801551 GCST90240983 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dynein light chain 1, cytoplasmic levels (DYNLL1.3881.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 dynein light chain 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020339 GCST90240984 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dynein light chain Tctex-type 3 levels (DYNLT3.12867.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dynein light chain Tctex-type 3 measurement http://www.ebi.ac.uk/efo/EFO_0802497 GCST90240985 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dyslexia-associated protein KIAA0319 levels (KIAA0319.10013.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dyslexia-associated protein KIAA0319 measurement http://www.ebi.ac.uk/efo/EFO_0802498 GCST90240986 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dyslexia-associated protein KIAA0319-like protein levels (KIAA0319L.13698.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dyslexia-associated protein KIAA0319-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802499 GCST90240987 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dystroglycan levels (DAG1.8369.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dystroglycan measurement http://www.ebi.ac.uk/efo/EFO_0802500 GCST90240988 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. E-selectin levels (SELE.3470.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90240989 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cortexin-3 levels (CTXN3.10467.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cortexin-3 measurement http://www.ebi.ac.uk/efo/EFO_0801500 GCST90240794 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Corticoliberin levels (CRH.5614.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 corticoliberin measurement http://www.ebi.ac.uk/efo/EFO_0802430 GCST90240795 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Corticosteroid-binding globulin levels (SERPINA6.4785.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 corticosteroid-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0020288 GCST90240796 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Corticotropin-releasing factor-binding protein levels (CRHBP.6039.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 corticotropin-releasing factor-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801501 GCST90240797 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Coxsackievirus and adenovirus receptor levels (CXADR.11204.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 coxsackievirus and adenovirus receptor measurement http://www.ebi.ac.uk/efo/EFO_0802431 GCST90240798 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Creatine kinase B-type levels (CKB.3800.71.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 creatine kinase b-type measurement http://www.ebi.ac.uk/efo/EFO_0020290 GCST90240799 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Creatine kinase M-type levels (CKM.2670.67.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 creatine kinase m-type measurement http://www.ebi.ac.uk/efo/EFO_0020291 GCST90240800 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CREB-binding protein levels (CREBBP.13614.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CREB-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801502 GCST90240801 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Crk-like protein levels (CRKL.9877.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CRK-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801503 GCST90240802 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cryptic protein levels (CFC1.3294.55.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cryptic protein measurement http://www.ebi.ac.uk/efo/EFO_0020293 GCST90240803 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CUB and sushi domain-containing protein 1 levels (CSMD1.9598.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CUB and Sushi domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803297 GCST90240804 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CUB and sushi domain-containing protein 2 levels (CSMD2.9971.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CUB and Sushi domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803314 GCST90240805 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CUB and zona pellucida-like domain-containing protein 1 levels (CUZD1.7943.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 CUB and zona pellucida-like domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803309 GCST90240806 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CUB domain-containing protein 1 levels (CDCP1.6565.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CUB domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802432 GCST90240807 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cubilin levels (CUBN.12904.180.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cubilin measurement http://www.ebi.ac.uk/efo/EFO_0802433 GCST90240808 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CUGBP Elav-like family member 2 levels (CELF2.7245.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CUGBP Elav-like family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802434 GCST90240809 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cullin-associated NEDD8-dissociated protein 1 levels (CAND1.13937.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cullin-associated NEDD8-dissociated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802438 GCST90240813 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CXADR-like membrane protein levels (CLMP.10440.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CXADR-like membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801504 GCST90240814 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CXADR-like membrane protein levels (CLMP.9585.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CXADR-like membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801504 GCST90240815 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclic AMP-dependent transcription factor ATF-6 alpha levels (ATF6.11277.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cyclic AMP-dependent transcription factor ATF-6 alpha measurement http://www.ebi.ac.uk/efo/EFO_0801505 GCST90240816 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclic AMP-responsive element-binding protein 3-like protein 1 levels (CREB3L1.11198.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cyclic AMP-responsive element-binding protein 3-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802439 GCST90240817 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclic AMP-responsive element-binding protein 3-like protein 4 levels (CREB3L4.11308.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 cyclic AMP-responsive element-binding protein 3-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801506 GCST90240818 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-C levels (CCNC.7817.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cyclin-C measurement http://www.ebi.ac.uk/efo/EFO_0801507 GCST90240819 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase 1:G2/mitotic-specific cyclin-B1 complex levels (CDC2.CCNB1.3422.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cyclin-dependent kinase 1:g2/mitotic-specific cyclin-B1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020294 GCST90240820 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase 2-associated protein 1 levels (CDK2AP1.9450.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cyclin-dependent kinase 2-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802440 GCST90240821 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase 2:Cyclin-A2 complex levels (CDK2.CCNA2.3357.67.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cyclin-dependent kinase 2:cyclin-A2 complex measurement http://www.ebi.ac.uk/efo/EFO_0020295 GCST90240822 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase 4 inhibitor B levels (CDKN2B.9874.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cyclin-dependent kinase 4 inhibitor B measurement http://www.ebi.ac.uk/efo/EFO_0802441 GCST90240823 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase 5:Cyclin-dependent kinase 5 activator 1 complex levels (CDK5.CDK5R1.3358.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cyclin-dependent kinase 5:cyclin-dependent kinase 5 activator 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020296 GCST90240824 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase 8:Cyclin-C complex levels (CDK8.CCNC.3359.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cyclin-dependent kinase 8:cyclin-c complex measurement http://www.ebi.ac.uk/efo/EFO_0020297 GCST90240825 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase inhibitor 1B levels (CDKN1B.3719.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cyclin-dependent kinase inhibitor 1b measurement http://www.ebi.ac.uk/efo/EFO_0020298 GCST90240826 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-dependent kinase inhibitor 3 levels (CDKN3.14178.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cyclin-dependent kinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802442 GCST90240827 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cyclin-H levels (CCNH.9848.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cyclin-H measurement http://www.ebi.ac.uk/efo/EFO_0801508 GCST90240828 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cystathionine beta-synthase levels (CBS.10086.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cystathionine beta-synthase measurement http://www.ebi.ac.uk/efo/EFO_0802443 GCST90240829 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cystatin-8 levels (CST8.10572.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cystatin-8 measurement http://www.ebi.ac.uk/efo/EFO_0801509 GCST90240830 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cystatin-D levels (CST5.13661.193.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90240831 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cystatin-F levels (CST7.3302.58.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90240832 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cystatin-M levels (CST6.3303.23.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90240833 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cystatin-M levels (CST6.14711.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90240834 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine and glycine-rich protein 2 levels (CSRP2.12968.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cysteine and glycine-rich protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802444 GCST90240835 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine and glycine-rich protein 3 levels (CSRP3.9171.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cysteine and glycine-rich protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0022027 GCST90240836 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine--tRNA ligase, cytoplasmic levels (CARS.14098.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cysteine--tRNA ligase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0802445 GCST90240837 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA repair protein XRCC1 levels (XRCC1.12535.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA repair protein XRCC1 measurement http://www.ebi.ac.uk/efo/EFO_0802479 GCST90240934 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA repair protein XRCC4 levels (XRCC4.9886.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 DNA repair protein XRCC4 measurement http://www.ebi.ac.uk/efo/EFO_0801532 GCST90240935 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA topoisomerase 1 levels (TOP1.2876.74.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA topoisomerase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020331 GCST90240936 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA topoisomerase 2-binding protein 1 levels (TOPBP1.9947.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA topoisomerase 2-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802480 GCST90240937 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-(apurinic or apyrimidinic site) lyase levels (APEX1.9849.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 DNA-(apurinic or apyrimidinic site) lyase measurement http://www.ebi.ac.uk/efo/EFO_0801533 GCST90240938 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-3-methyladenine glycosylase levels (MPG.12438.127.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 DNA-3-methyladenine glycosylase measurement http://www.ebi.ac.uk/efo/EFO_0801534 GCST90240939 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-binding protein inhibitor ID-1 levels (ID1.9436.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA-binding protein inhibitor ID-1 measurement http://www.ebi.ac.uk/efo/EFO_0802481 GCST90240940 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-binding protein inhibitor ID-2 levels (ID2.9426.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA-binding protein inhibitor ID-2 measurement http://www.ebi.ac.uk/efo/EFO_0802482 GCST90240941 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-binding protein SATB1 levels (SATB1.13511.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA-binding protein SATB1 measurement http://www.ebi.ac.uk/efo/EFO_0802483 GCST90240942 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-binding protein SATB2 levels (SATB2.10081.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA-binding protein SATB2 measurement http://www.ebi.ac.uk/efo/EFO_0802484 GCST90240943 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-directed DNA/RNA polymerase mu levels (POLM.12851.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA-directed DNA/RNA polymerase mu measurement http://www.ebi.ac.uk/efo/EFO_0802485 GCST90240944 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA-directed RNA polymerases I and III subunit RPAC1 levels (POLR1C.12939.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 DNA-directed RNA polymerases I and III subunit RPAC1 measurement http://www.ebi.ac.uk/efo/EFO_0801535 GCST90240945 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA/RNA-binding protein KIN17 levels (KIN.14643.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 DNA/RNA-binding protein KIN17 measurement http://www.ebi.ac.uk/efo/EFO_0801536 GCST90240946 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA/RNA-binding protein KIN17 levels (KIN.13476.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA/RNA-binding protein KIN17 measurement http://www.ebi.ac.uk/efo/EFO_0801536 GCST90240947 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily A member 4 levels (DNAJA4.9744.139.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily A member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802486 GCST90240948 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily B member 1 levels (DNAJB1.3852.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNAj homolog subfamily b member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020332 GCST90240949 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily B member 11 levels (DNAJB11.7110.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 DnaJ homolog subfamily B member 11 measurement http://www.ebi.ac.uk/efo/EFO_0801537 GCST90240950 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily B member 12 levels (DNAJB12.8006.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily B member 12 measurement http://www.ebi.ac.uk/efo/EFO_0802487 GCST90240951 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily B member 14 levels (DNAJB14.8053.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 DnaJ homolog subfamily B member 14 measurement http://www.ebi.ac.uk/efo/EFO_0801538 GCST90240952 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily B member 14 levels (DNAJB14.8037.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily B member 14 measurement http://www.ebi.ac.uk/efo/EFO_0801538 GCST90240953 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily B member 2 levels (DNAJB2.11438.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 DnaJ homolog subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801539 GCST90240954 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily B member 9 levels (DNAJB9.11214.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 DnaJ homolog subfamily B member 9 measurement http://www.ebi.ac.uk/efo/EFO_0801540 GCST90240955 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily C member 10 levels (DNAJC10.8297.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily C member 10 measurement http://www.ebi.ac.uk/efo/EFO_0802488 GCST90240956 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily C member 15 levels (DNAJC15.7197.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DnaJ homolog subfamily C member 15 measurement http://www.ebi.ac.uk/efo/EFO_0802489 GCST90240957 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DnaJ homolog subfamily C member 17 levels (DNAJC17.14655.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 DnaJ homolog subfamily C member 17 measurement http://www.ebi.ac.uk/efo/EFO_0801541 GCST90240958 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine-rich hydrophobic domain-containing protein 2 levels (CHIC2.10914.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cysteine-rich hydrophobic domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801510 GCST90240838 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine-rich motor neuron 1 protein levels (CRIM1.8699.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cysteine-rich motor neuron 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802446 GCST90240839 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine-rich secretory protein 2 levels (CRISP2.9282.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 cysteine-rich secretory protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801511 GCST90240840 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine-rich secretory protein 3 levels (CRISP3.3187.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cysteine-rich secretory protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020301 GCST90240841 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine-rich secretory protein LCCL domain-containing 2 levels (CRISPLD2.5691.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 cysteine-rich secretory protein LCCL domain-containing 2 measurement http://www.ebi.ac.uk/efo/EFO_0801512 GCST90240842 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cysteine-rich with EGF-like domain protein 1 levels (CRELD1.7628.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 cysteine-rich with EGF-like domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021870 GCST90240843 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome b-c1 complex subunit 7 levels (UQCRB.12957.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytochrome b-c1 complex subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0802447 GCST90240844 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome b5 levels (CYB5A.11287.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytochrome b5 measurement http://www.ebi.ac.uk/efo/EFO_0802448 GCST90240845 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome c levels (CYCS.2942.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytochrome C measurement http://www.ebi.ac.uk/efo/EFO_0020302 GCST90240846 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome c oxidase assembly factor 3 homolog, mitochondrial levels (COA3.7888.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cytochrome c oxidase assembly factor 3 homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801513 GCST90240847 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome c oxidase subunit 4 isoform 2, mitochondrial levels (COX4I2.7850.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cytochrome c oxidase subunit 4 isoform 2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801514 GCST90240848 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome c oxidase subunit 5B, mitochondrial levels (COX5B.7887.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytochrome c oxidase subunit 5B, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802449 GCST90240849 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome c oxidase subunit 6C levels (COX6C.8903.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cytochrome c oxidase subunit 6C measurement http://www.ebi.ac.uk/efo/EFO_0801515 GCST90240850 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome c oxidase subunit 7A1, mitochondrial levels (COX7A1.8390.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytochrome c oxidase subunit 7A1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802450 GCST90240851 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome c oxidase subunit 8A, mitochondrial levels (COX8A.10497.242.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cytochrome c oxidase subunit 8A, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801516 GCST90240852 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome P450 3A4 levels (CYP3A4.2943.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytochrome p450 3a4 measurement http://www.ebi.ac.uk/efo/EFO_0020303 GCST90240853 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytochrome P450 3A4 levels (CYP3A4.7879.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytochrome p450 3a4 measurement http://www.ebi.ac.uk/efo/EFO_0020303 GCST90240854 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytoglobin levels (CYGB.11546.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytoglobin measurement http://www.ebi.ac.uk/efo/EFO_0802451 GCST90240855 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytohesin-2 levels (CYTH2.12533.135.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cytohesin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801517 GCST90240856 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytohesin-4 levels (CYTH4.12746.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytohesin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802452 GCST90240857 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytohesin-interacting protein levels (CYTIP.13612.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytohesin-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0802453 GCST90240858 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytokine receptor common subunit beta levels (CSF2RB.10512.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cytokine receptor common subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801518 GCST90240859 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytokine receptor common subunit beta levels (CSF2RB.11137.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytokine receptor common subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801518 GCST90240860 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytokine receptor common subunit gamma levels (IL2RG.2634.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytokine receptor common subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0020304 GCST90240861 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytokine receptor-like factor 1 levels (CRLF1.CLCF1.2607.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytokine receptor-like factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802454 GCST90240862 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cullin-3 levels (CUL3.10045.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cullin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802435 GCST90240810 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cullin-4B levels (CUL4B.13743.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cullin-4B measurement http://www.ebi.ac.uk/efo/EFO_0802436 GCST90240811 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cullin-9 levels (CUL9.12991.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cullin-9 measurement http://www.ebi.ac.uk/efo/EFO_0802437 GCST90240812 Genome-wide genotyping array 2022-04-25 34981446 Nazarian A 2022-01-03 J Appl Genet www.ncbi.nlm.nih.gov/pubmed/34981446 Genome-wide analysis of genetic predisposition to common polygenic cancers. Breast cancer 677 European ancestry cases, 7,842 European ancestry controls NA Affymetrix, Illumina [2575640] (imputed) 6 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90101893 Genome-wide genotyping array 2022-04-25 34981446 Nazarian A 2022-01-03 J Appl Genet www.ncbi.nlm.nih.gov/pubmed/34981446 Genome-wide analysis of genetic predisposition to common polygenic cancers. Prostate cancer 820 European ancestry cases, 5,567 European ancestry controls NA Affymetrix, Illumina [2574194] (imputed) 3 prostate cancer http://purl.obolibrary.org/obo/MONDO_0008315 GCST90101894 Genome-wide genotyping array 2022-04-25 34981446 Nazarian A 2022-01-03 J Appl Genet www.ncbi.nlm.nih.gov/pubmed/34981446 Genome-wide analysis of genetic predisposition to common polygenic cancers. Colorectal cancer 397 European ancestry cases, 14,694 European ancestry controls NA Affymetrix, Illumina [2574310] (imputed) 5 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90101895 Genome-wide genotyping array 2022-04-25 34981446 Nazarian A 2022-01-03 J Appl Genet www.ncbi.nlm.nih.gov/pubmed/34981446 Genome-wide analysis of genetic predisposition to common polygenic cancers. Lung cancer 457 European ancestry cases, 14,632 European ancestry controls NA Affymetrix, Illumina [2574554] (imputed) 1 lung cancer http://purl.obolibrary.org/obo/MONDO_0008903 GCST90101896 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium voltage-gated channel subfamily E member 2 levels (KCNE2.10427.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 potassium voltage-gated channel subfamily E member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801901 GCST90242328 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium voltage-gated channel subfamily E member 3 levels (KCNE3.8067.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 potassium voltage-gated channel subfamily E member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802889 GCST90242329 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium voltage-gated channel subfamily E regulatory beta subunit 5 levels (KCNE5.8908.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 potassium voltage-gated channel subfamily E regulatory beta subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0801902 GCST90242330 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium voltage-gated channel subfamily E regulatory beta subunit 5 levels (KCNE5.8756.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 potassium voltage-gated channel subfamily E regulatory beta subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0801902 GCST90242331 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium voltage-gated channel subfamily F member 1 levels (KCNF1.12834.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 potassium voltage-gated channel subfamily F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802890 GCST90242332 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium voltage-gated channel subfamily G member 4 levels (KCNG4.13525.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 potassium voltage-gated channel subfamily G member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802891 GCST90242333 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium-transporting ATPase subunit beta levels (ATP4B.9994.217.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 potassium-transporting ATPase subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801903 GCST90242334 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. POU domain, class 2, transcription factor 1 levels (POU2F1.11715.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 POU domain, class 2, transcription factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802892 GCST90242335 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PR domain zinc finger protein 1 levels (PRDM1.14197.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 PR domain zinc finger protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801904 GCST90242336 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PR domain zinc finger protein 4 levels (PRDM4.12779.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 PR domain zinc finger protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802893 GCST90242337 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pre-mRNA-processing factor 6 levels (PRPF6.9581.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pre-mRNA-processing factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0802894 GCST90242338 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 levels (DHX38.13645.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 measurement http://www.ebi.ac.uk/efo/EFO_0801905 GCST90242339 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prefoldin subunit 5 levels (PFDN5.4271.75.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 prefoldin subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0020652 GCST90242340 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 11 levels (PSG11.7846.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pregnancy-specific beta-1-glycoprotein 11 measurement http://www.ebi.ac.uk/efo/EFO_0802895 GCST90242341 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 2 levels (PSG2.6405.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pregnancy-specific beta-1-glycoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802896 GCST90242342 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 3 levels (PSG3.6444.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 pregnancy-specific beta-1-glycoprotein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801906 GCST90242343 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 4 levels (PSG4.5649.83.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 pregnancy-specific beta-1-glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801907 GCST90242344 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 5 levels (PSG5.9314.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 pregnancy-specific beta-1-glycoprotein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801908 GCST90242345 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 6 levels (PSG6.6456.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pregnancy-specific beta-1-glycoprotein 6 measurement http://www.ebi.ac.uk/efo/EFO_0802897 GCST90242346 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 8 levels (PSG8.6238.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pregnancy-specific beta-1-glycoprotein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802898 GCST90242347 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pregnancy-specific beta-1-glycoprotein 9 levels (PSG9.9335.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 pregnancy-specific beta-1-glycoprotein 9 measurement http://www.ebi.ac.uk/efo/EFO_0801909 GCST90242348 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prenylcysteine oxidase-like levels (PCYOX1L.5599.88.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 prenylcysteine oxidase-like measurement http://www.ebi.ac.uk/efo/EFO_0801910 GCST90242349 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prestin levels (SLC26A5.9127.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prestin measurement http://www.ebi.ac.uk/efo/EFO_0802899 GCST90242350 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pro-FMRFamide-related neuropeptide FF levels (NPFF.5617.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 pro-FMRFamide-related neuropeptide FF measurement http://www.ebi.ac.uk/efo/EFO_0801911 GCST90242351 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pro-neuregulin-2, membrane-bound isoform levels (NRG2.8060.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pro-neuregulin-2, membrane-bound isoform measurement http://www.ebi.ac.uk/efo/EFO_0802900 GCST90242352 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 levels (PLOD3.10612.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802913 GCST90242378 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proenkephalin-A levels (PENK.9076.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 proenkephalin-A measurement http://www.ebi.ac.uk/efo/EFO_0801923 GCST90242379 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Profilin-2 levels (PFN2.13054.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 profilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802914 GCST90242380 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Progonadoliberin-1 levels (GNRH1.5627.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 progonadoliberin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801924 GCST90242381 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Progonadoliberin-2 levels (GNRH2.10708.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 progonadoliberin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801925 GCST90242382 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Programmed cell death 1 ligand 1 levels (CD274.5060.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90242383 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Programmed cell death 1 ligand 2 levels (PDCD1LG2.3004.67.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 programmed cell death 1 ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0008268 GCST90242384 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Programmed cell death protein 1 levels (PDCD1.9227.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 programmed cell death protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801926 GCST90242385 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Programmed cell death protein 5 levels (PDCD5.12517.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 programmed cell death protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801927 GCST90242386 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prokineticin-1 levels (PROK1.2247.20.11) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prokineticin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020655 GCST90242387 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolactin levels (PRL.2585.2.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prolactin measurement http://www.ebi.ac.uk/efo/EFO_0007003 GCST90242388 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolactin receptor levels (PRLR.5114.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 prolactin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020656 GCST90242389 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolactin-releasing peptide levels (PRLH.6543.182.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prolactin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0802915 GCST90242390 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolargin levels (PRELP.5675.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 prolargin measurement http://www.ebi.ac.uk/efo/EFO_0801928 GCST90242391 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proliferating cell nuclear antigen levels (PCNA.2915.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proliferating cell nuclear antigen measurement http://www.ebi.ac.uk/efo/EFO_0020657 GCST90242392 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proline-rich protein 1 levels (PROL1.6530.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proline-rich protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802916 GCST90242393 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolow-density lipoprotein receptor-related protein 1 levels (LRP1.10699.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 prolow-density lipoprotein receptor-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801929 GCST90242394 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolyl 4-hydroxylase subunit alpha-1 levels (P4HA1.11645.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prolyl 4-hydroxylase subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0802917 GCST90242395 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolyl 4-hydroxylase subunit alpha-2 levels (P4HA2.11348.132.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prolyl 4-hydroxylase subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0802918 GCST90242396 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prolyl endopeptidase FAP levels (FAP.5029.3.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prolyl endopeptidase FAP measurement http://www.ebi.ac.uk/efo/EFO_0021856 GCST90242397 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Promotilin levels (MLN.5631.83.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 promotilin measurement http://www.ebi.ac.uk/efo/EFO_0801930 GCST90242398 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Properdin levels (CFP.2960.66.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 properdin measurement http://www.ebi.ac.uk/efo/EFO_0008269 GCST90242399 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proprotein convertase subtilisin/kexin type 7 levels (PCSK7.4459.68.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90242400 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prostaglandin F2 receptor negative regulator levels (PTGFRN.12727.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 prostaglandin F2 receptor negative regulator measurement http://www.ebi.ac.uk/efo/EFO_0801931 GCST90242401 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prostaglandin reductase 1 levels (PTGR1.13543.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 prostaglandin reductase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801932 GCST90242402 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prostaglandin-H2 D-isomerase levels (PTGDS.10514.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 prostaglandin-H2 D-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0801933 GCST90242403 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prostate and testis expressed protein 1 levels (PATE1.8386.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prostate and testis expressed protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802919 GCST90242404 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prostate and testis expressed protein 4 levels (PATE4.8065.245.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 prostate and testis expressed protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803301 GCST90242405 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prostate-associated microseminoprotein levels (MSMP.8080.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prostate-associated microseminoprotein measurement http://www.ebi.ac.uk/efo/EFO_0802920 GCST90242406 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prostate-specific antigen levels (KLK3.8468.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prostate-specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0020660 GCST90242407 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protachykinin-1 levels (TAC1.9337.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protachykinin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801934 GCST90242408 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome activator complex subunit 1 levels (PSME1.5918.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90242409 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome activator complex subunit 3 levels (PSME3.5204.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteasome activator complex subunit 3 measurement http://www.ebi.ac.uk/efo/EFO_0020662 GCST90242410 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome assembly chaperone 3 levels (PSMG3.12729.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteasome assembly chaperone 3 measurement http://www.ebi.ac.uk/efo/EFO_0802921 GCST90242411 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome subunit alpha type-1 levels (PSMA1.7880.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 proteasome subunit alpha type-1 measurement http://www.ebi.ac.uk/efo/EFO_0020663 GCST90242412 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome subunit alpha type-1 levels (PSMA1.3859.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteasome subunit alpha type-1 measurement http://www.ebi.ac.uk/efo/EFO_0020663 GCST90242413 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome subunit alpha type-2 levels (PSMA2.4280.47.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteasome subunit alpha type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020664 GCST90242414 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome subunit alpha type-4 levels (PSMA4.14099.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteasome subunit alpha type-4 measurement http://www.ebi.ac.uk/efo/EFO_0802922 GCST90242415 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome subunit alpha type-6 levels (PSMA6.3860.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteasome subunit alpha type-6 measurement http://www.ebi.ac.uk/efo/EFO_0020665 GCST90242416 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteasome subunit beta type-5 levels (PSMB5.12580.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteasome subunit beta type-5 measurement http://www.ebi.ac.uk/efo/EFO_0802923 GCST90242417 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein amnionless levels (AMN.4322.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein amnionless measurement http://www.ebi.ac.uk/efo/EFO_0020667 GCST90242418 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein APCDD1 levels (APCDD1.6599.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein APCDD1 measurement http://www.ebi.ac.uk/efo/EFO_0802924 GCST90242419 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein arginine N-methyltransferase 3 levels (PRMT3.12696.166.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein arginine N-methyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802925 GCST90242420 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein argonaute-1 levels (AGO1.11651.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein argonaute-1 measurement http://www.ebi.ac.uk/efo/EFO_0802926 GCST90242421 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein C-ets-2 levels (ETS2.12350.86.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein C-ets-2 measurement http://www.ebi.ac.uk/efo/EFO_0801935 GCST90242422 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein CASC4 levels (CASC4.10613.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein CASC4 measurement http://www.ebi.ac.uk/efo/EFO_0802927 GCST90242423 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein CASC4 levels (CASC4.8838.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein CASC4 measurement http://www.ebi.ac.uk/efo/EFO_0802927 GCST90242424 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein CEI levels (C5orf38.6378.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein CEI measurement http://www.ebi.ac.uk/efo/EFO_0801936 GCST90242425 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein CREG1 levels (CREG1.9357.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 protein CREG1 measurement http://www.ebi.ac.uk/efo/EFO_0801937 GCST90242426 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein crumbs homolog 1 levels (CRB1.12012.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein crumbs homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0802928 GCST90242427 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein CYR61 levels (CYR61.6264.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein CYR61 measurement http://www.ebi.ac.uk/efo/EFO_0802929 GCST90242428 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein deglycase DJ-1 levels (PARK7.5016.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein deglycase DJ-1 measurement http://www.ebi.ac.uk/efo/EFO_0021982 GCST90242429 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein deglycase DJ-1 levels (PARK7.9845.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein deglycase DJ-1 measurement http://www.ebi.ac.uk/efo/EFO_0021982 GCST90242430 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein delta homolog 1 levels (DLK1.6496.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein delta homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0801938 GCST90242431 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein delta homolog 1 levels (DLK1.8380.244.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein delta homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0801938 GCST90242432 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein delta homolog 2 levels (DLK2.9359.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein delta homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0802930 GCST90242433 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein DEPP levels (DEPP.7178.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 protein DEPP measurement http://www.ebi.ac.uk/efo/EFO_0801939 GCST90242434 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein DGCR14 levels (DGCR14.11356.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein DGCR14 measurement http://www.ebi.ac.uk/efo/EFO_0801940 GCST90242435 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein DGCR6 levels (DGCR6.9444.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein DGCR6 measurement http://www.ebi.ac.uk/efo/EFO_0802931 GCST90242436 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein disulfide-isomerase A3 levels (PDIA3.7832.181.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein disulfide-isomerase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020668 GCST90242437 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein disulfide-isomerase A5 levels (PDIA5.5593.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein disulfide-isomerase A5 measurement http://www.ebi.ac.uk/efo/EFO_0801941 GCST90242438 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein disulfide-isomerase-like protein of the testis levels (PDILT.7092.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein disulfide-isomerase-like protein of the testis measurement http://www.ebi.ac.uk/efo/EFO_0802932 GCST90242439 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein dpy-30 homolog levels (DPY30.13943.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein dpy-30 homolog measurement http://www.ebi.ac.uk/efo/EFO_0802933 GCST90242440 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein enabled homolog levels (ENAH.9757.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein enabled homolog measurement http://www.ebi.ac.uk/efo/EFO_0802934 GCST90242441 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein eva-1 homolog C levels (EVA1C.7008.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 protein eva-1 homolog C measurement http://www.ebi.ac.uk/efo/EFO_0801942 GCST90242442 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein eva-1 homolog C levels (EVA1C.8877.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein eva-1 homolog C measurement http://www.ebi.ac.uk/efo/EFO_0801942 GCST90242443 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein EVI2B levels (EVI2B.13028.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein EVI2B measurement http://www.ebi.ac.uk/efo/EFO_0801943 GCST90242444 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM107A levels (FAM107A.2760.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein fam107a measurement http://www.ebi.ac.uk/efo/EFO_0020673 GCST90242445 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM107B levels (FAM107B.4774.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein fam107b measurement http://www.ebi.ac.uk/efo/EFO_0020674 GCST90242446 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM107B levels (FAM107B.7801.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein fam107b measurement http://www.ebi.ac.uk/efo/EFO_0020674 GCST90242447 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM134B levels (FAM134B.8556.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM134B measurement http://www.ebi.ac.uk/efo/EFO_0802935 GCST90242448 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM150B levels (FAM150B.6284.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein FAM150B measurement http://www.ebi.ac.uk/efo/EFO_0801944 GCST90242449 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM151A levels (FAM151A.7856.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein FAM151A measurement http://www.ebi.ac.uk/efo/EFO_0801945 GCST90242450 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM163A levels (FAM163A.6260.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 protein FAM163A measurement http://www.ebi.ac.uk/efo/EFO_0801946 GCST90242451 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM163B levels (FAM163B.10880.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM163B measurement http://www.ebi.ac.uk/efo/EFO_0802936 GCST90242452 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM171B levels (FAM171B.8851.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein FAM171B measurement http://www.ebi.ac.uk/efo/EFO_0801947 GCST90242453 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM171B levels (FAM171B.8061.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM171B measurement http://www.ebi.ac.uk/efo/EFO_0801947 GCST90242454 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM171B levels (FAM171B.8786.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM171B measurement http://www.ebi.ac.uk/efo/EFO_0801947 GCST90242455 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM172A levels (FAM172A.5615.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM172A measurement http://www.ebi.ac.uk/efo/EFO_0802937 GCST90242456 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM173A levels (FAM173A.7148.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM173A measurement http://www.ebi.ac.uk/efo/EFO_0802938 GCST90242457 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM177A1 levels (FAM177A1.8039.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 protein FAM177A1 measurement http://www.ebi.ac.uk/efo/EFO_0801948 GCST90242458 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM189A2 levels (FAM189A2.5699.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein FAM189A2 measurement http://www.ebi.ac.uk/efo/EFO_0801949 GCST90242459 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM189A2 levels (FAM189A2.5719.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM189A2 measurement http://www.ebi.ac.uk/efo/EFO_0801949 GCST90242460 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM19A2 levels (FAM19A2.6430.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM19A2 measurement http://www.ebi.ac.uk/efo/EFO_0802939 GCST90242461 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM19A3 levels (FAM19A3.7839.99.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM19A3 measurement http://www.ebi.ac.uk/efo/EFO_0802940 GCST90242462 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM19A4 levels (FAM19A4.6511.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM19A4 measurement http://www.ebi.ac.uk/efo/EFO_0802941 GCST90242463 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM19A5 levels (FAM19A5.5609.92.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM19A5 measurement http://www.ebi.ac.uk/efo/EFO_0802942 GCST90242464 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM209B levels (FAM209B.7066.199.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM209B measurement http://www.ebi.ac.uk/efo/EFO_0802943 GCST90242465 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM24B levels (FAM24B.8775.61.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM24B measurement http://www.ebi.ac.uk/efo/EFO_0802944 GCST90242466 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM3B levels (FAM3B.9177.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 8 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90242467 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM3B levels (FAM3B.5618.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90242468 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein FAM3D levels (FAM3D.13102.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90242469 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein G6b levels (G6B.8659.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein G6b measurement http://www.ebi.ac.uk/efo/EFO_0802945 GCST90242470 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein G6b levels (G6B.9466.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein G6b measurement http://www.ebi.ac.uk/efo/EFO_0802945 GCST90242471 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein GPR107 levels (GPR107.12963.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein GPR107 measurement http://www.ebi.ac.uk/efo/EFO_0802946 GCST90242472 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein HEG homolog 1 levels (HEG1.8947.268.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein HEG homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0802947 GCST90242473 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein jagged-1 levels (JAG1.5092.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein jagged-1 measurement http://www.ebi.ac.uk/efo/EFO_0008271 GCST90242474 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein jagged-2 levels (JAG2.5093.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein jagged-2 measurement http://www.ebi.ac.uk/efo/EFO_0020675 GCST90242475 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein JTB levels (JTB.9038.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein JTB measurement http://www.ebi.ac.uk/efo/EFO_0802948 GCST90242476 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kinase C alpha type levels (PRKCA.2644.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein kinase c alpha type measurement http://www.ebi.ac.uk/efo/EFO_0020677 GCST90242477 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pro-opiomelanocortin levels (POMC.9204.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pro-opiomelanocortin measurement http://www.ebi.ac.uk/efo/EFO_0022037 GCST90242353 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proactivator polypeptide-like 1 levels (PSAPL1.8814.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 proactivator polypeptide-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801912 GCST90242354 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable ATP-dependent RNA helicase DDX58 levels (DDX58.12382.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 probable ATP-dependent RNA helicase DDX58 measurement http://www.ebi.ac.uk/efo/EFO_0801913 GCST90242355 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable ATP-dependent RNA helicase DHX58 levels (DHX58.14012.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable ATP-dependent RNA helicase DHX58 measurement http://www.ebi.ac.uk/efo/EFO_0802901 GCST90242356 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable carboxypeptidase X1 levels (CPXM1.6255.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 probable carboxypeptidase X1 measurement http://www.ebi.ac.uk/efo/EFO_0801914 GCST90242357 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable dimethyladenosine transferase levels (DIMT1.12694.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 probable dimethyladenosine transferase measurement http://www.ebi.ac.uk/efo/EFO_0801915 GCST90242358 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable E3 ubiquitin-protein ligase HERC1 levels (HERC1.12705.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable E3 ubiquitin-protein ligase HERC1 measurement http://www.ebi.ac.uk/efo/EFO_0802902 GCST90242359 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable E3 ubiquitin-protein ligase HERC4 levels (HERC4.7860.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable E3 ubiquitin-protein ligase HERC4 measurement http://www.ebi.ac.uk/efo/EFO_0802903 GCST90242360 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable E3 ubiquitin-protein ligase MID2 levels (MID2.14249.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable E3 ubiquitin-protein ligase MID2 measurement http://www.ebi.ac.uk/efo/EFO_0802904 GCST90242361 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable G-protein coupled receptor 101 levels (GPR101.11371.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable G-protein coupled receptor 101 measurement http://www.ebi.ac.uk/efo/EFO_0802905 GCST90242362 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable G-protein coupled receptor 101 levels (GPR101.11670.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable G-protein coupled receptor 101 measurement http://www.ebi.ac.uk/efo/EFO_0802905 GCST90242363 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable G-protein coupled receptor 135 levels (GPR135.11465.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 probable G-protein coupled receptor 135 measurement http://www.ebi.ac.uk/efo/EFO_0801916 GCST90242364 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable inactive ribonuclease-like protein 13 levels (RNASE13.6424.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable inactive ribonuclease-like protein 13 measurement http://www.ebi.ac.uk/efo/EFO_0802906 GCST90242365 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable inactive serine protease 37 levels (PRSS37.5653.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable inactive serine protease 37 measurement http://www.ebi.ac.uk/efo/EFO_0802907 GCST90242366 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable palmitoyltransferase ZDHHC14 levels (ZDHHC14.11677.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable palmitoyltransferase ZDHHC14 measurement http://www.ebi.ac.uk/efo/EFO_0802908 GCST90242367 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable RNA-binding protein 19 levels (RBM19.11468.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 probable RNA-binding protein 19 measurement http://www.ebi.ac.uk/efo/EFO_0802909 GCST90242368 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable RNA-binding protein 23 levels (RBM23.11590.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 probable RNA-binding protein 23 measurement http://www.ebi.ac.uk/efo/EFO_0801917 GCST90242369 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable RNA-binding protein EIF1AD levels (EIF1AD.13545.97.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 probable RNA-binding protein EIF1AD measurement http://www.ebi.ac.uk/efo/EFO_0801918 GCST90242370 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Probable serine carboxypeptidase CPVL levels (CPVL.8891.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 probable serine carboxypeptidase CPVL measurement http://www.ebi.ac.uk/efo/EFO_0801919 GCST90242371 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Procalcitonin levels (CALCA.10494.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 procalcitonin measurement http://www.ebi.ac.uk/efo/EFO_0802910 GCST90242372 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Procollagen C-endopeptidase enhancer 1 levels (PCOLCE.11237.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 procollagen C-endopeptidase enhancer 1 measurement http://www.ebi.ac.uk/efo/EFO_0801920 GCST90242373 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Procollagen C-endopeptidase enhancer 2 levels (PCOLCE2.6081.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 procollagen C-endopeptidase enhancer 2 measurement http://www.ebi.ac.uk/efo/EFO_0801921 GCST90242374 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Procollagen galactosyltransferase 1 levels (COLGALT1.5638.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 procollagen galactosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801922 GCST90242375 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Procollagen galactosyltransferase 2 levels (COLGALT2.7234.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 procollagen galactosyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802911 GCST90242376 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 levels (PLOD2.6923.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802912 GCST90242377 Genome-wide genotyping array 2022-01-28 33887194 Hu Y 2021-04-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33887194 Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Hematocrit 33,324 Amish, White ancestry individuals, 654 Asian ancestry individuals, 14,474 Black individuals, 14,035 Central American ancestry, Cuban ancestry, Dominican ancestry, Mexican ancestry, Puerto Rican ancestry, South American ancestry individuals NA Illumina [110396782] 15 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90093293 Genome-wide sequencing 2022-01-28 33887194 Hu Y 2021-04-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33887194 Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Hemoglobin 33,325 Amish, White ancestry individuals, 653 Asian ancestry individuals, 14,454 Black individuals, 14,029 Central American ancestry, Cuban ancestry, Dominican ancestry, Mexican ancestry, Puerto Rican ancestry, South American ancestry individuals NA Illumina [110351653] 18 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90093294 Genome-wide sequencing 2022-01-28 33887194 Hu Y 2021-04-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33887194 Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Mean corpuscular hemoglobin 20,714 Amish, White ancestry individuals, 447 Asian ancestry individuals, 11,246 Black individuals, 13,834 Central American ancestry, Cuban ancestry, Dominican ancestry, Mexican ancestry, Puerto Rican ancestry, South American ancestry individuals NA Illumina [94681438] 57 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90093295 Genome-wide sequencing 2022-01-28 33887194 Hu Y 2021-04-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33887194 Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Mean corpuscular hemoglobin concentration 25,256 Amish, White ancestry individuals, 447 Asian ancestry individuals, 13,112 Black individuals, 13,833 Central American ancestry, Cuban ancestry, Dominican ancestry, Mexican ancestry, Puerto Rican ancestry, South American ancestry individuals NA Illumina [101200590] 15 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90093296 Genome-wide sequencing 2022-01-28 33887194 Hu Y 2021-04-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33887194 Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Mean corpuscular volume 22,267 Amish, White ancestry individuals, 447 Asian ancestry individuals, 12,285 Black individuals, 13,831 Central American ancestry, Cuban ancestry, Dominican ancestry, Mexican ancestry, Puerto Rican ancestry, South American ancestry individuals NA Illumina [97506867] 58 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90093297 Genome-wide sequencing 2022-01-28 33887194 Hu Y 2021-04-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33887194 Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Red blood cell count 20,220 Amish, White ancestry individuals, 384 Asian ancestry individuals, 10,747 Black individuals, 13,119 Central American ancestry, Cuban ancestry, Dominican ancestry, Mexican ancestry, Puerto Rican ancestry, South American ancestry individuals NA Illumina [92652022] 20 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90093298 Genome-wide sequencing 2022-01-28 33887194 Hu Y 2021-04-21 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33887194 Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program. Red cell distribution width 10,184 White ancestry individuals, 44 Asian ancestry individuals, 6,776 Black individuals, 11,978 Central American ancestry, Cuban ancestry, Dominican ancestry, Mexican ancestry, Puerto Rican ancestry, South American ancestry individuals NA Illumina [76131582] 23 obsolete_red blood cell distribution width http://www.ebi.ac.uk/efo/EFO_0005192 GCST90093299 Genome-wide sequencing 2022-01-14 34698592 Yang J 2021-10-26 Stress www.ncbi.nlm.nih.gov/pubmed/34698592 Genome-wide association studies of stress score in a Korean Cohort. High general stress 8,104 Korean ancestry individuals NA Affymetrix [320700] 3 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90093103 Genome-wide genotyping array 2022-01-14 34698592 Yang J 2021-10-26 Stress www.ncbi.nlm.nih.gov/pubmed/34698592 Genome-wide association studies of stress score in a Korean Cohort. High mental stress 8,104 Korean ancestry individuals NA Affymetrix [320700] 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90093104 Genome-wide genotyping array 2022-01-14 34698592 Yang J 2021-10-26 Stress www.ncbi.nlm.nih.gov/pubmed/34698592 Genome-wide association studies of stress score in a Korean Cohort. High physical stress 8,104 Korean ancestry individuals NA Affymetrix [320700] 5 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90093105 Genome-wide genotyping array 2022-01-14 34698592 Yang J 2021-10-26 Stress www.ncbi.nlm.nih.gov/pubmed/34698592 Genome-wide association studies of stress score in a Korean Cohort. High activity stress 8,104 Korean ancestry individuals NA Affymetrix [320700] 2 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90093106 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (minimum) 43,775 European ancestry individuals, 612 Asian ancestry individuals, 291 Black individuals, 215 Mixed ancestry individuals, 292 individuals NA Affymetrix [11247984] (imputed) 35 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100572 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (mean) 43,775 European ancestry individuals, 612 Asian ancestry individuals, 291 Black individuals, 215 Mixed ancestry individuals, 292 individuals NA Affymetrix [11247984] (imputed) 34 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100573 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (maximum) 43,775 European ancestry individuals, 612 Asian ancestry individuals, 291 Black individuals, 215 Mixed ancestry individuals, 292 individuals NA Affymetrix [11247984] (imputed) 34 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100574 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness 43,775 European ancestry individuals, 612 Asian ancestry individuals, 291 Black individuals, 215 Mixed ancestry individuals, 292 individuals NA Affymetrix [7320435] (imputed) 1 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100575 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness 98,843 European ancestry individuals, 612 Asian ancestry individuals, 291 Black individuals, 215 Mixed ancestry individuals, 292 individuals NA Affymetrix [6725452] (imputed) 15 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100576 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (minimum) 21,123 European ancestry men, 356 Asian ancestry men, 291 Black men, 215 Mixed ancestry men, 292 men NA Affymetrix [11247984] (imputed) 1 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100577 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (minimum) 22,652 European ancestry women, 256 Asian ancestry women, 153 Black women, 138 Mixed ancestry women, 159 women NA Affymetrix [11247984] (imputed) 0 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100578 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (mean) 21,123 European ancestry men, 356 Asian ancestry men, 291 Black men, 215 Mixed ancestry men, 292 men NA Affymetrix [11247984] (imputed) 5 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100579 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (mean) 22,652 European ancestry women, 256 Asian ancestry women, 153 Black women, 138 Mixed ancestry women, 159 women NA Affymetrix [11247984] (imputed) 0 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100580 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (maximum) 21,123 European ancestry men, 356 Asian ancestry men, 291 Black men, 215 Mixed ancestry men, 292 men NA Affymetrix [11247984] (imputed) 3 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100581 Genome-wide genotyping array 2022-04-01 34852643 Wai Yeung M 2021-12-02 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34852643 Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals. Carotid intima media thickness (maximum) 22,652 European ancestry women, 256 Asian ancestry women, 153 Black women, 138 Mixed ancestry women, 159 women NA Affymetrix [11247984] (imputed) 2 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90100582 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 6-pyruvoyl tetrahydrobiopterin synthase levels (PTS.12014.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 6-pyruvoyl tetrahydrobiopterin synthase measurement http://www.ebi.ac.uk/efo/EFO_0802242 GCST90240155 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 60S acidic ribosomal protein P2 levels (RPLP2.10949.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 60S acidic ribosomal protein P2 measurement http://www.ebi.ac.uk/efo/EFO_0802243 GCST90240156 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 60S ribosomal protein L30 levels (RPL30.12478.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 60S ribosomal protein L30 measurement http://www.ebi.ac.uk/efo/EFO_0801337 GCST90240157 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 72 kDa inositol polyphosphate 5-phosphatase levels (INPP5E.11370.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 72 kDa inositol polyphosphate 5-phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0802244 GCST90240158 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. 72 kDa type IV collagenase levels (MMP2.4160.49.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 72 kda type IV collagenase measurement http://www.ebi.ac.uk/efo/EFO_0020122 GCST90240159 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 1 levels (ADAMTS1.3174.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 1 measurement http://www.ebi.ac.uk/efo/EFO_0021968 GCST90240160 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 13 levels (ADAMTS13.3175.51.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 ADAMTS13 measurement http://www.ebi.ac.uk/efo/EFO_0009269 GCST90240161 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 15 levels (ADAMTS15.4533.76.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 15 measurement http://www.ebi.ac.uk/efo/EFO_0020123 GCST90240162 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 3 levels (ADAMTS3.8845.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 3 measurement http://www.ebi.ac.uk/efo/EFO_0802245 GCST90240163 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 4 levels (ADAMTS4.2809.25.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 4 measurement http://www.ebi.ac.uk/efo/EFO_0020124 GCST90240164 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 5 levels (ADAMTS5.3168.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90240165 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 6 levels (ADAMTS6.6441.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 6 measurement http://www.ebi.ac.uk/efo/EFO_0801338 GCST90240166 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. A/G-specific adenine DNA glycosylase levels (MUTYH.10030.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 A/G-specific adenine DNA glycosylase measurement http://www.ebi.ac.uk/efo/EFO_0802246 GCST90240167 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. AarF domain-containing protein kinase 4 levels (ADCK4.9794.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 aarF domain-containing protein kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0802247 GCST90240168 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial levels (PDK1.5227.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 [pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1; mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0021984 GCST005806 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Abelson tyrosine-protein kinase 2 levels (ABL2.5261.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Abelson tyrosine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008012 GCST90240169 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acetyl-CoA carboxylase 2 levels (ACACB.12900.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 acetyl-CoA carboxylase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802248 GCST90240170 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acid ceramidase levels (ASAH1.5748.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 acid ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0801339 GCST90240171 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arachidonate 15-lipoxygenase B levels (ALOX15B.12422.143.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 arachidonate 15-lipoxygenase B measurement http://www.ebi.ac.uk/efo/EFO_0801391 GCST90240325 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arf-GAP domain and FG repeat-containing protein 1 levels (AGFG1.11681.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 arf-GAP domain and FG repeat-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803312 GCST90240326 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 levels (ACAP2.12343.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803311 GCST90240327 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 levels (ASAP2.13518.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803306 GCST90240328 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arfaptin-1 levels (ARFIP1.13488.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 arfaptin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801392 GCST90240329 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arfaptin-2 levels (ARFIP2.12630.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 arfaptin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801393 GCST90240330 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Arginine/serine-rich protein 1 levels (RSRP1.9050.170.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 arginine/serine-rich protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802286 GCST90240331 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adenylate kinase isoenzyme 1 levels (AK1.5012.67.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 adenylate kinase isoenzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020129 GCST90240192 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adenylosuccinate synthetase isozyme 1 levels (ADSSL1.13998.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 adenylosuccinate synthetase isozyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0802256 GCST90240193 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adenylosuccinate synthetase isozyme 2 levels (ADSS.12644.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 adenylosuccinate synthetase isozyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0801345 GCST90240194 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adenylyltransferase and sulfurtransferase MOCS3 levels (MOCS3.14229.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 adenylyltransferase and sulfurtransferase MOCS3 measurement http://www.ebi.ac.uk/efo/EFO_0802257 GCST90240195 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adhesion G protein-coupled receptor F5 levels (ADGRF5.6409.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 adhesion G protein-coupled receptor F5 measurement http://www.ebi.ac.uk/efo/EFO_0801346 GCST90240196 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adhesion G-protein coupled receptor F1 levels (ADGRF1.11243.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 adhesion G-protein coupled receptor F1 measurement http://www.ebi.ac.uk/efo/EFO_0801347 GCST90240197 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adhesion G-protein coupled receptor G5 levels (ADGRG5.4551.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 adhesion G-protein coupled receptor G5 measurement http://www.ebi.ac.uk/efo/EFO_0021980 GCST90240198 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adipocyte plasma membrane-associated protein levels (APMAP.10605.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 adipocyte plasma membrane-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801348 GCST90240199 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-dependent glucokinase levels (ADPGK.6221.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ADP-dependent glucokinase measurement http://www.ebi.ac.uk/efo/EFO_0802258 GCST90240200 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribose pyrophosphatase, mitochondrial levels (NUDT9.9482.110.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ADP-ribose pyrophosphatase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801349 GCST90240201 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 levels (CD38.11505.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021923 GCST90240202 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 levels (CD38.11513.92.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021923 GCST90240203 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 levels (BST1.4535.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90240204 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor 3 levels (ARF3.12578.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ADP-ribosylation factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802259 GCST90240205 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor 6 levels (ARF6.12425.104.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ADP-ribosylation factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0801350 GCST90240206 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor GTPase-activating protein 2 levels (ARFGAP2.11664.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ADP-ribosylation factor GTPase-activating protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801351 GCST90240207 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor-binding protein GGA1 levels (GGA1.13594.158.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ADP-ribosylation factor-binding protein GGA1 measurement http://www.ebi.ac.uk/efo/EFO_0801352 GCST90240208 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor-binding protein GGA3 levels (GGA3.11683.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ADP-ribosylation factor-binding protein GGA3 measurement http://www.ebi.ac.uk/efo/EFO_0801353 GCST90240209 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor-like protein 1 levels (ARL1.12392.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ADP-ribosylation factor-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801354 GCST90240210 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor-like protein 11 levels (ARL11.12433.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ADP-ribosylation factor-like protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0801355 GCST90240211 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADP-ribosylation factor-like protein 3 levels (ARL3.12571.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ADP-ribosylation factor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801356 GCST90240212 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adrenomedullin levels (ADM.14115.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 adrenomedullin measurement http://www.ebi.ac.uk/efo/EFO_0010909 GCST90240213 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adseverin levels (SCIN.12684.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 adseverin measurement http://www.ebi.ac.uk/efo/EFO_0801358 GCST90240214 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Advanced glycosylation end product-specific receptor, soluble levels (AGER.4125.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 advanced glycosylation end product-specific receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0020131 GCST90240215 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aggrecan core protein levels (ACAN.3280.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 aggrecan core protein measurement http://www.ebi.ac.uk/efo/EFO_0020133 GCST90240216 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium-dependent phospholipase A2 levels (PLA2G5.2449.1.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcium-dependent phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020216 GCST90240551 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium-regulated heat stable protein 1 levels (CARHSP1.12808.103.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcium-regulated heat stable protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802358 GCST90240552 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A levels (PDE1A.5253.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1A measurement http://www.ebi.ac.uk/efo/EFO_0802359 GCST90240553 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium/calmodulin-dependent protein kinase kinase 1 levels (CAMKK1.3877.67.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcium/calmodulin-dependent protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020217 GCST90240554 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium/calmodulin-dependent protein kinase type 1 levels (CAMK1.3592.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 calcium/calmodulin-dependent protein kinase type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008062 GCST90240555 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acid sphingomyelinase-like phosphodiesterase 3a levels (SMPDL3A.14086.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90240172 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acid sphingomyelinase-like phosphodiesterase 3a levels (SMPDL3A.4771.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90240173 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acid-sensing ion channel 4 levels (ASIC4.6951.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 acid-sensing ion channel 4 measurement http://www.ebi.ac.uk/efo/EFO_0802249 GCST90240174 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acidic leucine-rich nuclear phosphoprotein 32 family member A levels (ANP32A.13073.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 acidic leucine-rich nuclear phosphoprotein 32 family member A measurement http://www.ebi.ac.uk/efo/EFO_0802250 GCST90240175 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acidic leucine-rich nuclear phosphoprotein 32 family member B levels (ANP32B.4194.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 acidic leucine-rich nuclear phosphoprotein 32 family member b measurement http://www.ebi.ac.uk/efo/EFO_0020125 GCST90240176 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Actin-binding LIM protein 3 levels (ABLIM3.13578.98.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 actin-binding LIM protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802251 GCST90240177 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Actin-related protein 2/3 complex subunit 3 levels (ARPC3.13573.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 actin-related protein 2/3 complex subunit 3 measurement http://www.ebi.ac.uk/efo/EFO_0802252 GCST90240178 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Activated Protein C levels (PROC.3758.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 activated protein C measurement http://www.ebi.ac.uk/efo/EFO_0020126 GCST90240179 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Activated Protein C levels (PROC.3758.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 activated protein C measurement http://www.ebi.ac.uk/efo/EFO_0020126 GCST90240180 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Activating signal cointegrator 1 complex subunit 1 levels (ASCC1.10647.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 activating signal cointegrator 1 complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0801340 GCST90240181 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Activator of 90 kDa heat shock protein ATPase homolog 1 levels (AHSA1.11633.89.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 activator of 90 kDa heat shock protein ATPase homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0801341 GCST90240182 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Activator of apoptosis harakiri levels (HRK.8008.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 activator of apoptosis harakiri measurement http://www.ebi.ac.uk/efo/EFO_0802253 GCST90240183 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Activin receptor type-1B levels (ACVR1B.2806.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 activin receptor type-1B measurement http://www.ebi.ac.uk/efo/EFO_0020127 GCST90240184 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acyl-CoA-binding domain-containing protein 6 levels (ACBD6.10075.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 acyl-CoA-binding domain-containing protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801342 GCST90240185 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acyl-CoA-binding domain-containing protein 7 levels (ACBD7.13563.259.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 acyl-CoA-binding domain-containing protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0801343 GCST90240186 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Acylphosphatase-2 levels (ACYP2.12812.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 acylphosphatase-2 measurement http://www.ebi.ac.uk/efo/EFO_0801344 GCST90240187 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ADAMTS-like protein 1 levels (ADAMTSL1.6575.79.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ADAMTS-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802254 GCST90240188 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adapter molecule crk levels (CRK.4976.57.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 adapter molecule CRK measurement http://www.ebi.ac.uk/efo/EFO_0020128 GCST90240189 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adenosine 3'-phospho 5'-phosphosulfate transporter 2 levels (SLC35B3.10660.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 adenosine 3'-phospho 5'-phosphosulfate transporter 2 measurement http://www.ebi.ac.uk/efo/EFO_0802255 GCST90240190 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Adenosine deaminase CECR1 levels (CECR1.6077.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 adenosine deaminase measurement http://www.ebi.ac.uk/efo/EFO_0010761 GCST90240191 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 7 levels (CCL7.4886.3.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST90240501 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-C motif chemokine 8 levels (CCL8.2785.15.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-C motif chemokine 8 measurement http://www.ebi.ac.uk/efo/EFO_0008055 GCST90240502 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-reactive protein levels (CRP.4337.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90240503 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 10 member A levels (CLEC10A.10955.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 10 member A measurement http://www.ebi.ac.uk/efo/EFO_0802342 GCST90240504 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 12 member A levels (CLEC12A.11187.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 C-type lectin domain family 12 member A measurement http://www.ebi.ac.uk/efo/EFO_0801433 GCST90240505 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 14 member A levels (CLEC14A.10461.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 14 member A measurement http://www.ebi.ac.uk/efo/EFO_0802343 GCST90240506 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 2 member A levels (CLEC2A.10953.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 2 member A measurement http://www.ebi.ac.uk/efo/EFO_0802344 GCST90240507 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 2 member B levels (CLEC2B.7786.83.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 2 member B measurement http://www.ebi.ac.uk/efo/EFO_0802345 GCST90240508 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 2 member D levels (CLEC2D.7054.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-type lectin domain family 2 member D measurement http://www.ebi.ac.uk/efo/EFO_0801434 GCST90240509 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 2 member L levels (CLEC2L.8242.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 2 member L measurement http://www.ebi.ac.uk/efo/EFO_0802346 GCST90240510 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 4 member D levels (CLEC4D.7752.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 4 member D measurement http://www.ebi.ac.uk/efo/EFO_0802347 GCST90240511 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 4 member E levels (CLEC4E.7077.9.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-type lectin domain family 4 member E measurement http://www.ebi.ac.uk/efo/EFO_0801435 GCST90240512 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 4 member K levels (CD207.3361.26.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-type lectin domain family 4 member K measurement http://www.ebi.ac.uk/efo/EFO_0020201 GCST90240513 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 4 member M levels (CLEC4M.3030.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-type lectin domain family 4 member M measurement http://www.ebi.ac.uk/efo/EFO_0020202 GCST90240514 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 5 member A levels (CLEC5A.8282.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-type lectin domain family 5 member A measurement http://www.ebi.ac.uk/efo/EFO_0801436 GCST90240515 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 6 member A levels (CLEC6A.6911.103.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 6 member A measurement http://www.ebi.ac.uk/efo/EFO_0802348 GCST90240516 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin domain family 7 member A levels (CLEC7A.3603.60.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin domain family 7 member A measurement http://www.ebi.ac.uk/efo/EFO_0802349 GCST90240517 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type lectin-like domain family 1 levels (CLECL1.14308.192.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-type lectin-like domain family 1 measurement http://www.ebi.ac.uk/efo/EFO_0802350 GCST90240518 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-type mannose receptor 2 levels (MRC2.3041.55.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-type mannose receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020204 GCST90240519 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 10 levels (CXCL10.4141.79.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST90240520 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 11 levels (CXCL11.3038.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90240521 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 13 levels (CXCL13.3487.32.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-X-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020205 GCST90240522 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 14 levels (CXCL14.5730.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-X-C motif chemokine 14 measurement http://www.ebi.ac.uk/efo/EFO_0802351 GCST90240523 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 16 levels (CXCL16.2436.49.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90240524 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 5 levels (CXCL5.2979.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 C-X-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008058 GCST90240525 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 9 levels (CXCL9.9188.119.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-X-C motif chemokine 9 measurement http://www.ebi.ac.uk/efo/EFO_0022032 GCST90240526 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C-X-C motif chemokine 9 levels (CXCL9.11593.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C-X-C motif chemokine 9 measurement http://www.ebi.ac.uk/efo/EFO_0022032 GCST90240527 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C1GALT1-specific chaperone 1 levels (C1GALT1C1.5735.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 C1GALT1-specific chaperone 1 measurement http://www.ebi.ac.uk/efo/EFO_0801437 GCST90240528 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. C3a anaphylatoxin des Arginine levels (C3.2755.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 C3a anaphylatoxin des arginine measurement http://www.ebi.ac.uk/efo/EFO_0020206 GCST90240529 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-1 levels (CDH1.2501.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90240530 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-12 levels (CDH12.10701.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cadherin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020210 GCST90240531 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-12 levels (CDH12.3656.9.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cadherin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020210 GCST90240532 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-15 levels (CDH15.11215.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0020211 GCST90240533 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-15 levels (CDH15.5410.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0020211 GCST90240534 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-2 levels (CDH2.3797.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cadherin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020212 GCST90240535 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-3 levels (CDH3.2643.57.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cadherin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020213 GCST90240536 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-5 levels (CDH5.2819.23.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cadherin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008060 GCST90240537 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-7 levels (CDH7.7959.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 cadherin-7 measurement http://www.ebi.ac.uk/efo/EFO_0801438 GCST90240538 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-related family member 1 levels (CDHR1.8372.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cadherin-related family member 1 measurement http://www.ebi.ac.uk/efo/EFO_0801439 GCST90240539 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-related family member 3 levels (CDHR3.8222.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cadherin-related family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802352 GCST90240540 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-related family member 3 levels (CDHR3.9463.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cadherin-related family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802352 GCST90240541 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cadherin-related family member 5 levels (CDHR5.9962.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cadherin-related family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801440 GCST90240542 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calbindin levels (CALB1.9918.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 calbindin measurement http://www.ebi.ac.uk/efo/EFO_0801441 GCST90240543 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcineurin B homologous protein 1 levels (CHP1.12458.79.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcineurin B homologous protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802353 GCST90240544 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcineurin B homologous protein 3 levels (TESC.12831.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcineurin B homologous protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802354 GCST90240545 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcineurin subunit B type 1 levels (PPP3R1.3657.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcineurin subunit B type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020215 GCST90240546 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcipressin-1 levels (RCAN1.13465.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 calcipressin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801442 GCST90240547 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium uptake protein 3, mitochondrial levels (EFHA2.6912.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcium uptake protein 3, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802355 GCST90240548 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium-binding and coiled-coil domain-containing protein 2 levels (CALCOCO2.12534.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcium-binding and coiled-coil domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802356 GCST90240549 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium-binding protein 8 levels (CALN1.10933.107.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcium-binding protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802357 GCST90240550 Genome-wide genotyping array 2021-11-25 34033851 Cordell HJ 2021-05-22 J Hepatol www.ncbi.nlm.nih.gov/pubmed/34033851 An international genome-wide meta-analysis of primary biliary cholangitis: novel risk loci and candidate drugs. Primary biliary cholangitis 8,021 European ancestry cases, 16,489 European ancestry controls NA NR [5054572] (imputed) 57 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST90061440 Genome-wide genotyping array 2021-11-25 34033851 Cordell HJ 2021-05-22 J Hepatol www.ncbi.nlm.nih.gov/pubmed/34033851 An international genome-wide meta-analysis of primary biliary cholangitis: novel risk loci and candidate drugs. Primary biliary cholangitis 2,495 East Asian ancestry cases, 4,283 East Asian ancestry controls NA NR [5275424] (imputed) 20 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST90061441 Genome-wide genotyping array 2021-11-25 34033851 Cordell HJ 2021-05-22 J Hepatol www.ncbi.nlm.nih.gov/pubmed/34033851 An international genome-wide meta-analysis of primary biliary cholangitis: novel risk loci and candidate drugs. Primary biliary cholangitis 8,021 European ancestry cases, 16,489 European ancestry controls, 2,495 East Asian ancestry cases, 4,283 East Asian ancestry controls NA NR [2787054] (imputed) 48 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST90061442 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Replication initiator 1 levels (REPIN1.13554.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 replication initiator 1 measurement http://www.ebi.ac.uk/efo/EFO_0802001 GCST90242628 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Repulsive guidance molecule A levels (RGMA.5483.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 repulsive guidance molecule A measurement http://www.ebi.ac.uk/efo/EFO_0008273 GCST90242629 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Resistin levels (RETN.3046.31.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90242630 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retbindin levels (RTBDN.8613.97.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 retbindin measurement http://www.ebi.ac.uk/efo/EFO_0803009 GCST90242631 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Reticulocalbin-2 levels (RCN2.10645.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 reticulocalbin-2 measurement http://www.ebi.ac.uk/efo/EFO_0803010 GCST90242632 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Reticulon-4 receptor levels (RTN4R.5105.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90242633 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retina-specific copper amine oxidase levels (AOC2.6434.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 retina-specific copper amine oxidase measurement http://www.ebi.ac.uk/efo/EFO_0803011 GCST90242634 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta levels (PDE6D.13491.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta measurement http://www.ebi.ac.uk/efo/EFO_0802002 GCST90242635 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinaldehyde-binding protein 1 levels (RLBP1.12936.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 retinaldehyde-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802003 GCST90242636 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinoblastoma-associated protein levels (RB1.5024.67.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 retinoblastoma-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0020706 GCST90242637 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinoblastoma-binding protein 5 levels (RBBP5.13631.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 retinoblastoma-binding protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803012 GCST90242638 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinoblastoma-like protein 1 levels (RBL1.12879.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 retinoblastoma-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803013 GCST90242639 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinoic acid receptor responder protein 1 levels (RARRES1.8398.277.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 retinoic acid receptor responder protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802004 GCST90242640 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinoic acid receptor responder protein 3 levels (RARRES3.10961.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 retinoic acid receptor responder protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802005 GCST90242641 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinoid-binding protein 7 levels (RBP7.14208.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 retinoid-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802006 GCST90242642 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinol dehydrogenase 16 levels (RDH16.12881.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 retinol dehydrogenase 16 measurement http://www.ebi.ac.uk/efo/EFO_0802007 GCST90242643 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinol-binding protein 4 levels (RBP4.5482.61.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 retinol-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020707 GCST90242644 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retinoschisin levels (RS1.6497.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 retinoschisin measurement http://www.ebi.ac.uk/efo/EFO_0803014 GCST90242645 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Retroviral-like aspartic protease 1 levels (ASPRV1.13023.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 retroviral-like aspartic protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0802008 GCST90242646 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RGM domain family member B levels (RGMB.3331.8.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rgm domain family member b measurement http://www.ebi.ac.uk/efo/EFO_0020708 GCST90242647 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho GDP-dissociation inhibitor 1 levels (ARHGDIA.6454.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rho GDP-dissociation inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802009 GCST90242648 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho GDP-dissociation inhibitor 2 levels (ARHGDIB.9846.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rho GDP-dissociation inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0802010 GCST90242649 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho GTPase-activating protein 1 levels (ARHGAP1.11955.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803015 GCST90242650 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho GTPase-activating protein 25 levels (ARHGAP25.11333.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rho GTPase-activating protein 25 measurement http://www.ebi.ac.uk/efo/EFO_0802011 GCST90242651 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho GTPase-activating protein 30 levels (ARHGAP30.12807.89.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 rho GTPase-activating protein 30 measurement http://www.ebi.ac.uk/efo/EFO_0802012 GCST90242652 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RAC-alpha/beta/gamma serine/threonine-protein kinase levels (AKT1.AKT2.AKT3.2867.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RAC-alpha/beta/gamma serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021972 GCST90242578 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RAC-beta serine/threonine-protein kinase levels (AKT2.14685.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 RAC-beta serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021989 GCST90242579 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RAC-beta serine/threonine-protein kinase levels (AKT2.5360.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RAC-beta serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021989 GCST90242580 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Radiation-inducible immediate-early gene IEX-1 levels (IER3.9786.310.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 radiation-inducible immediate-early gene IEX-1 measurement http://www.ebi.ac.uk/efo/EFO_0802987 GCST90242581 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ragulator complex protein LAMTOR3 levels (LAMTOR3.12490.92.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ragulator complex protein LAMTOR3 measurement http://www.ebi.ac.uk/efo/EFO_0801986 GCST90242582 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ran-binding protein 3 levels (RANBP3.14037.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ran-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802988 GCST90242583 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rap guanine nucleotide exchange factor 5 levels (RAPGEF5.9059.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rap guanine nucleotide exchange factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0802989 GCST90242584 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rap1 GTPase-activating protein 1 levels (RAP1GAP.13735.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rap1 GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801987 GCST90242585 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rap1 GTPase-GDP dissociation stimulator 1 levels (RAP1GDS1.14106.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rap1 GTPase-GDP dissociation stimulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0802990 GCST90242586 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras GTPase-activating protein 1 levels (RASA1.5481.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ras GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020698 GCST90242587 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related C3 botulinum toxin substrate 3 levels (RAC3.5271.5.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ras-related C3 botulinum toxin substrate 3 measurement http://www.ebi.ac.uk/efo/EFO_0021987 GCST90242588 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-14 levels (RAB14.14283.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ras-related protein Rab-14 measurement http://www.ebi.ac.uk/efo/EFO_0801988 GCST90242589 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-22A levels (RAB22A.12408.333.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ras-related protein Rab-22A measurement http://www.ebi.ac.uk/efo/EFO_0802991 GCST90242590 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-26 levels (RAB26.6997.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ras-related protein Rab-26 measurement http://www.ebi.ac.uk/efo/EFO_0801989 GCST90242591 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-27A levels (RAB27A.9504.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ras-related protein Rab-27A measurement http://www.ebi.ac.uk/efo/EFO_0802992 GCST90242592 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-27B levels (RAB27B.13596.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ras-related protein Rab-27B measurement http://www.ebi.ac.uk/efo/EFO_0802993 GCST90242593 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-35 levels (RAB35.13514.121.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ras-related protein Rab-35 measurement http://www.ebi.ac.uk/efo/EFO_0801990 GCST90242594 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-39B levels (RAB39B.12403.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ras-related protein Rab-39B measurement http://www.ebi.ac.uk/efo/EFO_0802994 GCST90242595 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rab-7b levels (RAB7B.12409.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ras-related protein Rab-7b measurement http://www.ebi.ac.uk/efo/EFO_0802995 GCST90242596 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ras-related protein Rap-2a levels (RAP2A.9885.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ras-related protein Rap-2a measurement http://www.ebi.ac.uk/efo/EFO_0802996 GCST90242597 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor tyrosine-protein kinase erbB-2 levels (ERBB2.2616.23.18) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor tyrosine-protein kinase erbb-2 measurement http://www.ebi.ac.uk/efo/EFO_0020700 GCST90242598 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor tyrosine-protein kinase erbB-3 levels (ERBB3.2617.56.35) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor tyrosine-protein kinase erbb-3 measurement http://www.ebi.ac.uk/efo/EFO_0020701 GCST90242599 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-interacting serine/threonine-protein kinase 2 levels (RIPK2.8970.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-interacting serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802997 GCST90242600 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-interacting serine/threonine-protein kinase 2 levels (RIPK2.8993.151.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-interacting serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802997 GCST90242601 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein kinase FLT3 levels (FLT3.3437.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 receptor-type tyrosine-protein kinase flt3 measurement http://www.ebi.ac.uk/efo/EFO_0020703 GCST90242602 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho GTPase-activating protein 36 levels (ARHGAP36.6289.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho GTPase-activating protein 36 measurement http://www.ebi.ac.uk/efo/EFO_0803016 GCST90242653 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho GTPase-activating protein 5 levels (ARHGAP5.14748.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho GTPase-activating protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803017 GCST90242654 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho guanine nucleotide exchange factor 1 levels (ARHGEF1.13976.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rho guanine nucleotide exchange factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802013 GCST90242655 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho guanine nucleotide exchange factor 10 levels (ARHGEF10.9061.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rho guanine nucleotide exchange factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0802014 GCST90242656 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho guanine nucleotide exchange factor 2 levels (ARHGEF2.12848.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho guanine nucleotide exchange factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0803018 GCST90242657 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho guanine nucleotide exchange factor 25 levels (ARHGEF25.13519.112.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho guanine nucleotide exchange factor 25 measurement http://www.ebi.ac.uk/efo/EFO_0803019 GCST90242658 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho guanine nucleotide exchange factor 7 levels (ARHGEF7.13932.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho guanine nucleotide exchange factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0803020 GCST90242659 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho-associated protein kinase 2 levels (ROCK2.13654.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho-associated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0803021 GCST90242660 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho-related GTP-binding protein Rho6 levels (RND1.13574.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho-related GTP-binding protein Rho6 measurement http://www.ebi.ac.uk/efo/EFO_0803022 GCST90242661 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho-related GTP-binding protein RhoD levels (RHOD.12442.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho-related GTP-binding protein RhoD measurement http://www.ebi.ac.uk/efo/EFO_0803023 GCST90242662 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rho-related GTP-binding protein RhoG levels (RHOG.12540.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 rho-related GTP-binding protein RhoG measurement http://www.ebi.ac.uk/efo/EFO_0803024 GCST90242663 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rhophilin-2 levels (RHPN2.11439.88.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rhophilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802015 GCST90242664 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Riboflavin kinase levels (RFK.13059.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 riboflavin kinase measurement http://www.ebi.ac.uk/efo/EFO_0802016 GCST90242665 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonuclease 4 levels (RNASE4.5644.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ribonuclease 4 measurement http://www.ebi.ac.uk/efo/EFO_0802017 GCST90242666 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonuclease H1 levels (RNASEH1.8470.213.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ribonuclease H1 measurement http://www.ebi.ac.uk/efo/EFO_0022020 GCST90242667 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonuclease K6 levels (RNASE6.5646.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ribonuclease K6 measurement http://www.ebi.ac.uk/efo/EFO_0802018 GCST90242668 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonuclease pancreatic levels (RNASE1.7211.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 ribonuclease pancreatic measurement http://www.ebi.ac.uk/efo/EFO_0802019 GCST90242669 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonuclease UK114 levels (HRSP12.14636.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ribonuclease UK114 measurement http://www.ebi.ac.uk/efo/EFO_0802020 GCST90242670 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonucleoside-diphosphate reductase large subunit levels (RRM1.11360.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ribonucleoside-diphosphate reductase large subunit measurement http://www.ebi.ac.uk/efo/EFO_0802021 GCST90242671 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonucleoside-diphosphate reductase subunit M2 B levels (RRM2B.8925.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ribonucleoside-diphosphate reductase subunit M2 B measurement http://www.ebi.ac.uk/efo/EFO_0802022 GCST90242672 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribonucleoside-diphosphate reductase subunit M2 B levels (RRM2B.8854.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ribonucleoside-diphosphate reductase subunit M2 B measurement http://www.ebi.ac.uk/efo/EFO_0802022 GCST90242673 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribose-5-phosphate isomerase levels (RPIA.12333.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ribose-5-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0802023 GCST90242674 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribosomal protein S6 kinase alpha-6 levels (RPS6KA6.12688.115.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ribosomal protein S6 kinase alpha-6 measurement http://www.ebi.ac.uk/efo/EFO_0802024 GCST90242675 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribosome biogenesis protein TSR3 homolog levels (TSR3.7018.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ribosome biogenesis protein TSR3 homolog measurement http://www.ebi.ac.uk/efo/EFO_0803025 GCST90242676 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribosome-binding protein 1 levels (RRBP1.9492.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ribosome-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803026 GCST90242677 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribosome-recycling factor, mitochondrial levels (MRRF.12355.223.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ribosome-recycling factor, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0803027 GCST90242678 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribosyldihydronicotinamide dehydrogenase [quinone] levels (NQO2.9754.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 ribosyldihydronicotinamide dehydrogenase [quinone] measurement http://www.ebi.ac.uk/efo/EFO_0803298 GCST90242679 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ribulose-phosphate 3-epimerase levels (RPE.12646.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ribulose-phosphate 3-epimerase measurement http://www.ebi.ac.uk/efo/EFO_0802025 GCST90242680 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rieske domain-containing protein levels (RFESD.13603.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rieske domain-containing protein measurement http://www.ebi.ac.uk/efo/EFO_0802026 GCST90242681 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RING finger protein 122 levels (RNF122.11160.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RING finger protein 122 measurement http://www.ebi.ac.uk/efo/EFO_0803028 GCST90242682 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RING finger protein 148 levels (RNF148.7742.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RING finger protein 148 measurement http://www.ebi.ac.uk/efo/EFO_0803029 GCST90242683 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RING finger protein 148 levels (RNF148.9955.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RING finger protein 148 measurement http://www.ebi.ac.uk/efo/EFO_0803029 GCST90242684 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RING finger protein 150 levels (RNF150.9774.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RING finger protein 150 measurement http://www.ebi.ac.uk/efo/EFO_0803030 GCST90242685 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RING finger protein 165 levels (RNF165.11561.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 RING finger protein 165 measurement http://www.ebi.ac.uk/efo/EFO_0802027 GCST90242686 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RING finger protein 215 levels (RNF215.7758.217.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RING finger protein 215 measurement http://www.ebi.ac.uk/efo/EFO_0803031 GCST90242687 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RING finger protein 219 levels (RNF219.8822.163.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RING finger protein 219 measurement http://www.ebi.ac.uk/efo/EFO_0803032 GCST90242688 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA binding protein fox-1 homolog 2 levels (RBFOX2.11462.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RNA binding protein fox-1 homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0803033 GCST90242689 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA demethylase ALKBH5 levels (ALKBH5.8793.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RNA demethylase ALKBH5 measurement http://www.ebi.ac.uk/efo/EFO_0803034 GCST90242690 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA polymerase II elongation factor ELL levels (ELL.11459.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 RNA polymerase II elongation factor ELL measurement http://www.ebi.ac.uk/efo/EFO_0802028 GCST90242691 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA polymerase II elongation factor ELL2 levels (ELL2.11494.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RNA polymerase II elongation factor ELL2 measurement http://www.ebi.ac.uk/efo/EFO_0803035 GCST90242692 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA polymerase II subunit A C-terminal domain phosphatase SSU72 levels (SSU72.13566.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 RNA polymerase II subunit A C-terminal domain phosphatase SSU72 measurement http://www.ebi.ac.uk/efo/EFO_0802029 GCST90242693 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA-binding protein 24 levels (RBM24.11380.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 RNA-binding protein 24 measurement http://www.ebi.ac.uk/efo/EFO_0802030 GCST90242694 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA-binding protein 28 levels (RBM28.11927.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RNA-binding protein 28 measurement http://www.ebi.ac.uk/efo/EFO_0803036 GCST90242695 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA-binding protein 3 levels (RBM3.12747.89.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 RNA-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802031 GCST90242696 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA-binding protein 39 levels (RBM39.4284.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rna-binding protein 39 measurement http://www.ebi.ac.uk/efo/EFO_0020712 GCST90242697 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA-binding protein 40 levels (RNPC3.12814.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RNA-binding protein 40 measurement http://www.ebi.ac.uk/efo/EFO_0803037 GCST90242698 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA-binding protein EWS levels (EWSR1.12988.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 RNA-binding protein EWS measurement http://www.ebi.ac.uk/efo/EFO_0802032 GCST90242699 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RNA-binding protein Nova-1 levels (NOVA1.12557.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RNA-binding protein Nova-1 measurement http://www.ebi.ac.uk/efo/EFO_0803038 GCST90242700 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Roundabout homolog 1 levels (ROBO1.5740.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 roundabout homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0803039 GCST90242701 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Roundabout homolog 2 levels (ROBO2.5116.62.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 roundabout homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0020713 GCST90242702 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein phosphatase delta levels (PTPRD.9296.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-type tyrosine-protein phosphatase delta measurement http://www.ebi.ac.uk/efo/EFO_0802998 GCST90242603 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein phosphatase eta levels (PTPRJ.8250.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-type tyrosine-protein phosphatase eta measurement http://www.ebi.ac.uk/efo/EFO_0802999 GCST90242604 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein phosphatase H levels (PTPRH.11222.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 receptor-type tyrosine-protein phosphatase H measurement http://www.ebi.ac.uk/efo/EFO_0801991 GCST90242605 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein phosphatase H levels (PTPRH.11988.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-type tyrosine-protein phosphatase H measurement http://www.ebi.ac.uk/efo/EFO_0801991 GCST90242606 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein phosphatase R levels (PTPRR.6361.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-type tyrosine-protein phosphatase R measurement http://www.ebi.ac.uk/efo/EFO_0803000 GCST90242607 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein phosphatase S levels (PTPRS.6049.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-type tyrosine-protein phosphatase S measurement http://www.ebi.ac.uk/efo/EFO_0803001 GCST90242608 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Receptor-type tyrosine-protein phosphatase U levels (PTPRU.8337.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 receptor-type tyrosine-protein phosphatase U measurement http://www.ebi.ac.uk/efo/EFO_0803002 GCST90242609 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Recoverin levels (RCVRN.14334.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 recoverin measurement http://www.ebi.ac.uk/efo/EFO_0803003 GCST90242610 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RecQ-mediated genome instability protein 1 levels (RMI1.13926.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 recQ-mediated genome instability protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801992 GCST90242611 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Redox-regulatory protein FAM213A levels (FAM213A.13423.94.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 redox-regulatory protein FAM213A measurement http://www.ebi.ac.uk/efo/EFO_0801993 GCST90242612 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regenerating islet-derived protein 3-alpha levels (REG3A.9277.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 regenerating islet-derived protein 3-alpha measurement http://www.ebi.ac.uk/efo/EFO_0803004 GCST90242613 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regenerating islet-derived protein 4 levels (REG4.11102.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 regenerating islet-derived protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021921 GCST90242614 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulation of nuclear pre-mRNA domain-containing protein 1A levels (RPRD1A.13515.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 regulation of nuclear pre-mRNA domain-containing protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0801994 GCST90242615 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulator of G-protein signaling 10 levels (RGS10.11634.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 regulator of G-protein signaling 10 measurement http://www.ebi.ac.uk/efo/EFO_0803005 GCST90242616 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulator of G-protein signaling 18 levels (RGS18.13982.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 regulator of G-protein signaling 18 measurement http://www.ebi.ac.uk/efo/EFO_0801995 GCST90242617 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulator of G-protein signaling 19 levels (RGS19.12713.365.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 regulator of G-protein signaling 19 measurement http://www.ebi.ac.uk/efo/EFO_0801996 GCST90242618 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulator of G-protein signaling 3 levels (RGS3.12827.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 regulator of G-protein signaling 3 measurement http://www.ebi.ac.uk/efo/EFO_0803006 GCST90242619 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulator of G-protein signaling 8 levels (RGS8.11666.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 regulator of G-protein signaling 8 measurement http://www.ebi.ac.uk/efo/EFO_0801997 GCST90242620 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulator of microtubule dynamics protein 1 levels (RMDN1.7096.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 regulator of microtubule dynamics protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801998 GCST90242621 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulator of microtubule dynamics protein 3 levels (RMDN3.9290.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 regulator of microtubule dynamics protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803007 GCST90242622 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Regulatory factor X-associated protein levels (RFXAP.12726.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 regulatory factor X-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801999 GCST90242623 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Relaxin receptor 1 levels (RXFP1.14135.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 relaxin receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021950 GCST90242624 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RELT-like protein 1 levels (RELL1.13399.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 RELT-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802000 GCST90242625 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RELT-like protein 2 levels (RELL2.6600.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 RELT-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803008 GCST90242626 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Renin levels (REN.3396.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 renin measurement http://www.ebi.ac.uk/efo/EFO_0010616 GCST90242627 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement component C1q receptor levels (CD93.14136.234.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 complement component C1q receptor measurement http://www.ebi.ac.uk/efo/EFO_0802427 GCST90240773 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement component C6 levels (C6.4127.75.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 complement component C6 measurement http://www.ebi.ac.uk/efo/EFO_0020281 GCST90240774 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement component C8 levels (C8A.C8B.C8G.2429.27.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 complement component C8 measurement http://www.ebi.ac.uk/efo/EFO_0008094 GCST90240775 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement component C9 levels (C9.3060.43.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90240776 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement decay-accelerating factor levels (CD55.5069.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 complement decay-accelerating factor measurement http://www.ebi.ac.uk/efo/EFO_0008095 GCST90240777 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement factor B levels (CFB.4129.72.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 complement factor B measurement http://www.ebi.ac.uk/efo/EFO_0008096 GCST90240778 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement factor H levels (CFH.4159.130.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90240779 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement factor H-related protein 5 levels (CFHR5.3666.17.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90240780 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement factor H-related protein 5 levels (CFHR5.7885.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90240781 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement factor I levels (CFI.2567.5.6) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 complement factor I measurement http://www.ebi.ac.uk/efo/EFO_0008099 GCST90240782 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Connective tissue growth factor levels (CTGF.2975.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 connective tissue growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020284 GCST90240783 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Conserved oligomeric Golgi complex subunit 8 levels (COG8.9543.131.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 conserved oligomeric Golgi complex subunit 8 measurement http://www.ebi.ac.uk/efo/EFO_0802428 GCST90240784 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Contactin-2 levels (CNTN2.3296.92.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90240785 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Contactin-4 levels (CNTN4.3298.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 contactin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020287 GCST90240786 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Contactin-5 levels (CNTN5.3299.29.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 contactin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008101 GCST90240787 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Contactin-associated protein 1 levels (CNTNAP1.14617.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 contactin-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802429 GCST90240788 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Contactin-associated protein-like 2 levels (CNTNAP2.6965.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 contactin-associated protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801496 GCST90240789 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. COP9 signalosome complex subunit 2 levels (COPS2.14029.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 COP9 signalosome complex subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0801497 GCST90240790 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Copine-1 levels (CPNE1.5346.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90240791 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Core-binding factor subunit beta levels (CBFB.10048.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 core-binding factor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801498 GCST90240792 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Corneodesmosin levels (CDSN.7085.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 corneodesmosin measurement http://www.ebi.ac.uk/efo/EFO_0801499 GCST90240793 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Urea transporter 2 levels (SLC14A2.12818.159.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 urea transporter 2 measurement http://www.ebi.ac.uk/efo/EFO_0802203 GCST90243295 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uridine-cytidine kinase 2 levels (UCK2.12515.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uridine-cytidine kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0803238 GCST90243296 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Urokinase plasminogen activator surface receptor levels (PLAUR.2652.15.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90243297 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Urokinase-type plasminogen activator levels (PLAU.4158.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90243298 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytokine receptor-like factor 2 levels (CRLF2.2746.56.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytokine receptor-like factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020306 GCST90240863 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytokine receptor-like factor 2 levels (CRLF2.13694.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytokine receptor-like factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020306 GCST90240864 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytoplasmic tyrosine-protein kinase BMX levels (BMX.3414.40.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytoplasmic tyrosine-protein kinase BMX measurement http://www.ebi.ac.uk/efo/EFO_0020308 GCST90240865 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytoskeleton-associated protein 2 levels (CKAP2.5345.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cytoskeleton-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020309 GCST90240866 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytosolic non-specific dipeptidase levels (CNDP2.3192.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytosolic non-specific dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020310 GCST90240867 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytotoxic and regulatory T-cell molecule levels (CRTAM.5068.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytotoxic and regulatory t-cell molecule measurement http://www.ebi.ac.uk/efo/EFO_0020311 GCST90240868 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cytotoxic and regulatory T-cell molecule levels (CRTAM.7968.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cytotoxic and regulatory t-cell molecule measurement http://www.ebi.ac.uk/efo/EFO_0020311 GCST90240869 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. D-dimer levels (FGA.FGB.FGG.4907.56.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 D dimer measurement http://www.ebi.ac.uk/efo/EFO_0004507 GCST90240870 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. D-glucuronyl C5-epimerase levels (GLCE.7808.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 D-glucuronyl C5-epimerase measurement http://www.ebi.ac.uk/efo/EFO_0801519 GCST90240871 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DCC-interacting protein 13-alpha levels (APPL1.12825.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DCC-interacting protein 13-alpha measurement http://www.ebi.ac.uk/efo/EFO_0802455 GCST90240872 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DCN1-like protein 3 levels (DCUN1D3.13553.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DCN1-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802456 GCST90240873 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DCN1-like protein 5 levels (DCUN1D5.8760.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 DCN1-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801520 GCST90240874 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. dCTP pyrophosphatase 1 levels (DCTPP1.4314.12.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DCTP pyrophosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020314 GCST90240875 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DDB1- and CUL4-associated factor 5 levels (DCAF5.11283.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DDB1- and CUL4-associated factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0802457 GCST90240876 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Death-associated protein kinase 2 levels (DAPK2.4355.13.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 death-associated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008107 GCST90240877 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Decorin levels (DCN.2666.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 decorin measurement http://www.ebi.ac.uk/efo/EFO_0020315 GCST90240878 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dedicator of cytokinesis protein 9 levels (DOCK9.14002.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 dedicator of cytokinesis protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0801521 GCST90240879 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Deformed epidermal autoregulatory factor 1 homolog levels (DEAF1.6369.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 deformed epidermal autoregulatory factor 1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801522 GCST90240880 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Delta and Notch-like epidermal growth factor-related receptor levels (DNER.9769.48.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 delta and Notch-like epidermal growth factor-related receptor measurement http://www.ebi.ac.uk/efo/EFO_0802458 GCST90240881 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Delta and Notch-like epidermal growth factor-related receptor levels (DNER.11442.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 delta and Notch-like epidermal growth factor-related receptor measurement http://www.ebi.ac.uk/efo/EFO_0802458 GCST90240882 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Delta-like protein 1 levels (DLL1.5349.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90240883 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Delta-like protein 1 levels (DLL1.8264.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90240884 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Delta-like protein 4 levels (DLL4.3305.6.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 delta-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020317 GCST90240885 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-1(VIII) chain levels (COL8A1.4807.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collagen alpha-1(VIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020269 GCST90240746 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-1(XV) chain levels (COL15A1.8974.172.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 collagen alpha-1(XV) chain measurement http://www.ebi.ac.uk/efo/EFO_0801488 GCST90240747 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uromodulin-like 1 levels (UMODL1.9114.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uromodulin-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0803239 GCST90243299 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uronyl 2-sulfotransferase levels (UST.8364.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uronyl 2-sulfotransferase measurement http://www.ebi.ac.uk/efo/EFO_0803240 GCST90243300 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uroplakin-3b levels (UPK3B.8286.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 uroplakin-3b measurement http://www.ebi.ac.uk/efo/EFO_0803241 GCST90243301 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uroplakin-3b-like protein levels (UPK3BL.6633.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uroplakin-3b-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802204 GCST90243302 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Uroporphyrinogen-III synthase levels (UROS.11248.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 uroporphyrinogen-III synthase measurement http://www.ebi.ac.uk/efo/EFO_0802205 GCST90243303 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Urotensin-2 receptor levels (UTS2R.13530.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 urotensin-2 receptor measurement http://www.ebi.ac.uk/efo/EFO_0803242 GCST90243304 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UTP--glucose-1-phosphate uridylyltransferase levels (UGP2.13939.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UTP--glucose-1-phosphate uridylyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0803243 GCST90243305 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UV excision repair protein RAD23 homolog A levels (RAD23A.10058.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 UV excision repair protein RAD23 homolog A measurement http://www.ebi.ac.uk/efo/EFO_0803244 GCST90243306 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. UV excision repair protein RAD23 homolog B levels (RAD23B.12522.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 UV excision repair protein RAD23 homolog B measurement http://www.ebi.ac.uk/efo/EFO_0802206 GCST90243307 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. V-set and immunoglobulin domain-containing protein 1 levels (VSIG1.8367.142.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 v-set and immunoglobulin domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803245 GCST90243308 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. V-set and immunoglobulin domain-containing protein 2 levels (VSIG2.8018.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 v-set and immunoglobulin domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803308 GCST90243309 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. V-set and transmembrane domain-containing protein 2-like protein levels (VSTM2L.6549.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 v-set and transmembrane domain-containing protein 2-like protein measurement http://www.ebi.ac.uk/efo/EFO_0803246 GCST90243310 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. V-set and transmembrane domain-containing protein 4 levels (VSTM4.7242.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 v-set and transmembrane domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803247 GCST90243311 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vacuolar protein sorting-associated protein 29 levels (VPS29.14318.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vacuolar protein sorting-associated protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0802207 GCST90243312 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vacuolar protein sorting-associated protein 4A levels (VPS4A.11476.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vacuolar protein sorting-associated protein 4A measurement http://www.ebi.ac.uk/efo/EFO_0802208 GCST90243313 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vacuolar protein sorting-associated protein 4B levels (VPS4B.12668.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vacuolar protein sorting-associated protein 4B measurement http://www.ebi.ac.uk/efo/EFO_0802209 GCST90243314 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vacuolar protein sorting-associated protein VTA1 homolog levels (VTA1.4209.60.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vacuolar protein sorting-associated protein VTA1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020845 GCST90243315 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Valine--tRNA ligase levels (VARS.13083.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 valine--tRNA ligase measurement http://www.ebi.ac.uk/efo/EFO_0802210 GCST90243316 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular cell adhesion protein 1 levels (VCAM1.2967.8.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vascular cell adhesion protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020846 GCST90243317 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular endothelial growth factor A levels (VEGFA.2597.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90243318 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular endothelial growth factor A, isoform 121 levels (VEGFA.14032.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 vascular endothelial growth factor A, isoform 121 measurement http://www.ebi.ac.uk/efo/EFO_0020847 GCST90243319 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular endothelial growth factor C levels (VEGFC.3132.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vascular endothelial growth factor C measurement http://www.ebi.ac.uk/efo/EFO_0020848 GCST90243320 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular endothelial growth factor D levels (FIGF.13098.93.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90243321 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular endothelial growth factor D levels (FIGF.14705.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90243322 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Vascular endothelial growth factor receptor 2 levels (KDR.3651.50.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90243323 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-1(XX) chain levels (COL20A1.8804.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collagen alpha-1(XX) chain measurement http://www.ebi.ac.uk/efo/EFO_0802418 GCST90240748 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-1(XXVI) chain levels (COL26A1.9539.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collagen alpha-1(XXVI) chain measurement http://www.ebi.ac.uk/efo/EFO_0802419 GCST90240749 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-1(XXVIII) chain levels (COL28A1.10702.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collagen alpha-1(XXVIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0802420 GCST90240750 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-2(IX) chain levels (COL9A2.9804.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 collagen alpha-2(IX) chain measurement http://www.ebi.ac.uk/efo/EFO_0801489 GCST90240751 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-2(XI) chain levels (COL11A2.11278.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 collagen alpha-2(XI) chain measurement http://www.ebi.ac.uk/efo/EFO_0801490 GCST90240752 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-3(VI) chain levels (COL6A3.11196.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collagen alpha-3(VI) chain measurement http://www.ebi.ac.uk/efo/EFO_0802421 GCST90240753 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-5(VI) chain levels (COL6A5.11155.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collagen alpha-5(VI) chain measurement http://www.ebi.ac.uk/efo/EFO_0802422 GCST90240754 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagenase 3 levels (MMP13.4925.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collagenase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020271 GCST90240755 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collectin-10 levels (COLEC10.6558.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 collectin-10 measurement http://www.ebi.ac.uk/efo/EFO_0801491 GCST90240756 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collectin-11 levels (COLEC11.4430.44.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90240757 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collectin-12 levels (COLEC12.5457.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90240758 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collectin-12 levels (COLEC12.9787.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90240759 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collectrin levels (TMEM27.7816.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 collectrin measurement http://www.ebi.ac.uk/efo/EFO_0802423 GCST90240760 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. COMM domain-containing protein 1 levels (COMMD1.12509.115.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 COMM domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802424 GCST90240761 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. COMM domain-containing protein 7 levels (COMMD7.2823.7.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 COMM domain-containing protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020273 GCST90240762 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C1q and tumor necrosis factor-related protein 9A levels (C1QTNF9.6019.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 complement C1q and tumor necrosis factor-related protein 9A measurement http://www.ebi.ac.uk/efo/EFO_0803293 GCST90240763 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C1q subcomponent subunit C levels (C1QC.14100.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 complement C1q subcomponent subunit C measurement http://www.ebi.ac.uk/efo/EFO_0801492 GCST90240764 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C1q tumor necrosis factor-related protein 1 levels (C1QTNF1.6304.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 complement C1q tumor necrosis factor-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801493 GCST90240765 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C1q tumor necrosis factor-related protein 3 levels (C1QTNF3.7251.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 complement C1q tumor necrosis factor-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802425 GCST90240766 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C1q tumor necrosis factor-related protein 5 levels (C1QTNF5.7810.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 complement C1q tumor necrosis factor-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801494 GCST90240767 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C1q-like protein 4 levels (C1QL4.7132.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 complement C1q-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802426 GCST90240768 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C1r subcomponent-like protein levels (C1RL.9348.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 complement C1r subcomponent-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801495 GCST90240769 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement C4 levels (C4A.C4B.4481.34.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 27 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST90240770 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement component 1 Q subcomponent-binding protein, mitochondrial levels (C1QBP.4967.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 complement component 1 q subcomponent-binding protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020280 GCST90240771 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Complement component C1q receptor levels (CD93.11200.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 complement component C1q receptor measurement http://www.ebi.ac.uk/efo/EFO_0802427 GCST90240772 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protrudin levels (ZFYVE27.9102.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protrudin measurement http://www.ebi.ac.uk/efo/EFO_0802976 GCST90242553 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pseudokinase FAM20A levels (FAM20A.6433.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 pseudokinase FAM20A measurement http://www.ebi.ac.uk/efo/EFO_0801979 GCST90242554 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pterin-4-alpha-carbinolamine dehydratase levels (PCBD1.11313.100.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pterin-4-alpha-carbinolamine dehydratase measurement http://www.ebi.ac.uk/efo/EFO_0802978 GCST90242555 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pterin-4-alpha-carbinolamine dehydratase 2 levels (PCBD2.6899.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pterin-4-alpha-carbinolamine dehydratase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802977 GCST90242556 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pulmonary surfactant-associated protein C levels (SFTPC.5738.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 pulmonary surfactant-associated protein C measurement http://www.ebi.ac.uk/efo/EFO_0801980 GCST90242557 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pulmonary surfactant-associated protein D levels (SFTPD.4414.69.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90242558 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Purine nucleoside phosphorylase levels (PNP.10039.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 purine nucleoside phosphorylase measurement http://www.ebi.ac.uk/efo/EFO_0801981 GCST90242559 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Putative apolipoprotein(a)-like protein 2 levels (LPAL2.9246.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 putative apolipoprotein(a)-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802979 GCST90242560 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Putative chondrosarcoma-associated gene 1 protein levels (CSAG1.5716.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 putative chondrosarcoma-associated gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802980 GCST90242561 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Putative inactive group IIC secretory phospholipase A2 levels (PLA2G2C.8850.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 putative inactive group IIC secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0802981 GCST90242562 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Putative phospholipase B-like 2 levels (PLBD2.6536.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 putative phospholipase B-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0802982 GCST90242563 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Putative pregnancy-specific beta-1-glycoprotein 7 levels (PSG7.5651.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 putative pregnancy-specific beta-1-glycoprotein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802983 GCST90242564 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Putative uncharacterized protein PQLC2L levels (PQLC2L.7939.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 putative uncharacterized protein PQLC2L measurement http://www.ebi.ac.uk/efo/EFO_0802984 GCST90242565 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pyridoxal kinase levels (PDXK.11098.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 pyridoxal kinase measurement http://www.ebi.ac.uk/efo/EFO_0021919 GCST90242566 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pyridoxal phosphate phosphatase levels (PDXP.3897.61.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pyridoxal phosphate phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0020694 GCST90242567 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pyrin domain-containing protein 1 levels (PYDC1.12835.101.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pyrin domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802985 GCST90242568 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pyruvate carboxylase, mitochondrial levels (PC.13990.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pyruvate carboxylase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802986 GCST90242569 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pyruvate kinase PKLR levels (PKLR.11203.97.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 pyruvate kinase PKLR measurement http://www.ebi.ac.uk/efo/EFO_0801982 GCST90242570 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Quinone oxidoreductase-like protein 1 levels (CRYZL1.9207.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 quinone oxidoreductase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021880 GCST90242571 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. R-spondin-3 levels (RSPO3.13094.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 r-spondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0021878 GCST90242572 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. R-spondin-4 levels (RSPO4.8464.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 R-spondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0022019 GCST90242573 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RAB6-interacting golgin levels (GORAB.7247.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 RAB6-interacting Golgin measurement http://www.ebi.ac.uk/efo/EFO_0801983 GCST90242574 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rab9 effector protein with kelch motifs levels (RABEPK.13599.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 rab9 effector protein with kelch motifs measurement http://www.ebi.ac.uk/efo/EFO_0801984 GCST90242575 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Rac GTPase-activating protein 1 levels (RACGAP1.13587.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 rac GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801985 GCST90242576 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. RAC-alpha/beta/gamma serine/threonine-protein kinase levels (AKT1.AKT2.AKT3.3392.68.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 RAC-alpha/beta/gamma serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021972 GCST90242577 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein ripply1 levels (RIPPLY1.9767.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein ripply1 measurement http://www.ebi.ac.uk/efo/EFO_0802960 GCST90242503 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A11 levels (S100A11.14011.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein S100-A11 measurement http://www.ebi.ac.uk/efo/EFO_0801958 GCST90242504 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A12 levels (S100A12.5852.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90242505 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A13 levels (S100A13.7223.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 protein S100-A13 measurement http://www.ebi.ac.uk/efo/EFO_0801959 GCST90242506 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A2 levels (S100A2.11969.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein S100-A2 measurement http://www.ebi.ac.uk/efo/EFO_0802961 GCST90242507 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A4 levels (S100A4.14116.129.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein S100-A4 measurement http://www.ebi.ac.uk/efo/EFO_0021893 GCST90242508 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A5 levels (S100A5.14222.68.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein S100-A5 measurement http://www.ebi.ac.uk/efo/EFO_0801960 GCST90242509 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A6 levels (S100A6.13090.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein S100-A6 measurement http://www.ebi.ac.uk/efo/EFO_0021927 GCST90242510 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A7 levels (S100A7.5921.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein S100-A7 measurement http://www.ebi.ac.uk/efo/EFO_0022002 GCST90242511 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein S100-A9 levels (S100A9.5339.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein s100-a9 measurement http://www.ebi.ac.uk/efo/EFO_0020687 GCST90242512 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein SCO1 homolog, mitochondrial levels (SCO1.7853.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein SCO1 homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802962 GCST90242513 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein SEC13 homolog levels (SEC13.14689.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein SEC13 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801961 GCST90242514 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein sel-1 homolog 2 levels (SEL1L2.9082.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein sel-1 homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0801962 GCST90242515 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein SERAC1 levels (SERAC1.8985.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein SERAC1 measurement http://www.ebi.ac.uk/efo/EFO_0801963 GCST90242516 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein shisa-3 homolog levels (SHISA3.7057.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 protein shisa-3 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801964 GCST90242517 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein SPACA7 levels (SPACA7.6466.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein SPACA7 measurement http://www.ebi.ac.uk/efo/EFO_0801965 GCST90242518 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein sprouty homolog 1 levels (SPRY1.9512.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein sprouty homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0802963 GCST90242519 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein syndesmos levels (NUDT16L1.12497.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein syndesmos measurement http://www.ebi.ac.uk/efo/EFO_0801966 GCST90242520 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein TMEPAI levels (PMEPA1.6936.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein TMEPAI measurement http://www.ebi.ac.uk/efo/EFO_0801967 GCST90242521 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein transport protein Sec61 subunit beta levels (SEC61B.7878.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein transport protein Sec61 subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0802964 GCST90242522 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein transport protein Sec61 subunit gamma levels (SEC61G.8872.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein transport protein Sec61 subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0802965 GCST90242523 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein turtle homolog A levels (IGSF9.10518.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein turtle homolog A measurement http://www.ebi.ac.uk/efo/EFO_0802966 GCST90242524 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein tyrosine phosphatase type IVA 2 levels (PTP4A2.11699.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein tyrosine phosphatase type IVA 2 measurement http://www.ebi.ac.uk/efo/EFO_0802967 GCST90242525 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein unc-13 homolog A levels (UNC13A.14052.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein unc-13 homolog A measurement http://www.ebi.ac.uk/efo/EFO_0802968 GCST90242526 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein unc-93 homolog B1 levels (UNC93B1.13487.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein unc-93 homolog B1 measurement http://www.ebi.ac.uk/efo/EFO_0801968 GCST90242527 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein Wnt-7a levels (WNT7A.4889.82.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein wnt-7a measurement http://www.ebi.ac.uk/efo/EFO_0020689 GCST90242528 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein YIPF6 levels (YIPF6.9984.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein YIPF6 measurement http://www.ebi.ac.uk/efo/EFO_0802969 GCST90242529 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein Z-dependent protease inhibitor levels (SERPINA10.13119.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 12 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90242530 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein Z-dependent protease inhibitor levels (SERPINA10.6583.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90242531 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein-tyrosine kinase 2-beta levels (PTK2B.8918.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein-tyrosine kinase 2-beta measurement http://www.ebi.ac.uk/efo/EFO_0801969 GCST90242532 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein-tyrosine kinase 6 levels (PTK6.3832.51.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein-tyrosine kinase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020691 GCST90242533 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein-tyrosine sulfotransferase 1 levels (TPST1.7928.183.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein-tyrosine sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801970 GCST90242534 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein-tyrosine sulfotransferase 2 levels (TPST2.8024.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 protein-tyrosine sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801971 GCST90242535 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proteoglycan 3 levels (PRG3.9015.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 proteoglycan 3 measurement http://www.ebi.ac.uk/efo/EFO_0802970 GCST90242536 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Prothrombin levels (F2.5316.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 prothrombin measurement http://www.ebi.ac.uk/efo/EFO_0020692 GCST90242537 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Proto-oncogene tyrosine-protein kinase receptor Ret levels (RET.3220.40.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 proto-oncogene tyrosine-protein kinase receptor Ret measurement http://www.ebi.ac.uk/efo/EFO_0008272 GCST90242538 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin alpha-4 levels (PCDHA4.7157.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protocadherin alpha-4 measurement http://www.ebi.ac.uk/efo/EFO_0801972 GCST90242539 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin alpha-4 levels (PCDHA4.10533.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protocadherin alpha-4 measurement http://www.ebi.ac.uk/efo/EFO_0801972 GCST90242540 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin alpha-7 levels (PCDHA7.8758.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protocadherin alpha-7 measurement http://www.ebi.ac.uk/efo/EFO_0801973 GCST90242541 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin alpha-C2 levels (PCDHAC2.9361.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protocadherin alpha-C2 measurement http://www.ebi.ac.uk/efo/EFO_0802971 GCST90242542 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin beta-1 levels (PCDHB1.9941.70.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protocadherin beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0802972 GCST90242543 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin beta-10 levels (PCDHB10.9963.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protocadherin beta-10 measurement http://www.ebi.ac.uk/efo/EFO_0801974 GCST90242544 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin beta-2 levels (PCDHB2.10748.216.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protocadherin beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0801975 GCST90242545 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin beta-4 levels (PCDHB4.10522.167.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 protocadherin beta-4 measurement http://www.ebi.ac.uk/efo/EFO_0801976 GCST90242546 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin gamma-A8 levels (PCDHGA8.11259.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protocadherin gamma-A8 measurement http://www.ebi.ac.uk/efo/EFO_0802973 GCST90242547 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin gamma-C5 levels (PCDHGC5.7983.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protocadherin gamma-C5 measurement http://www.ebi.ac.uk/efo/EFO_0801977 GCST90242548 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin-10 levels (PCDH10.8780.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 protocadherin-10 measurement http://www.ebi.ac.uk/efo/EFO_0801978 GCST90242549 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin-10 levels (PCDH10.9018.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protocadherin-10 measurement http://www.ebi.ac.uk/efo/EFO_0801978 GCST90242550 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin-15 levels (PCDH15.14228.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protocadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0802974 GCST90242551 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protocadherin-9 levels (PCDH9.10558.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protocadherin-9 measurement http://www.ebi.ac.uk/efo/EFO_0802975 GCST90242552 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kinase C beta type (splice variant beta-II) levels (PRKCB.5475.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein kinase c beta type (splice variant beta-II) measurement http://www.ebi.ac.uk/efo/EFO_0020678 GCST90242478 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kinase C iota type levels (PRKCI.3379.29.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein kinase c iota type measurement http://www.ebi.ac.uk/efo/EFO_0020681 GCST90242479 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kinase C zeta type levels (PRKCZ.2645.54.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein kinase c zeta type measurement http://www.ebi.ac.uk/efo/EFO_0020683 GCST90242480 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kinase C-binding protein NELL1 levels (NELL1.6544.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein kinase C-binding protein NELL1 measurement http://www.ebi.ac.uk/efo/EFO_0801950 GCST90242481 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kinase C-binding protein NELL2 levels (NELL2.6022.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein kinase C-binding protein NELL2 measurement http://www.ebi.ac.uk/efo/EFO_0802949 GCST90242482 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kish-A levels (TMEM167A.11112.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein kish-A measurement http://www.ebi.ac.uk/efo/EFO_0802950 GCST90242483 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein kish-B levels (TMEM167B.13421.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein kish-B measurement http://www.ebi.ac.uk/efo/EFO_0802951 GCST90242484 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein Largen levels (PRR16.10621.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein Largen measurement http://www.ebi.ac.uk/efo/EFO_0802952 GCST90242485 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein LDOC1 levels (LDOC1.8378.3.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein LDOC1 measurement http://www.ebi.ac.uk/efo/EFO_0801951 GCST90242486 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein lin-7 homolog B levels (LIN7B.4238.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein lin-7 homolog B measurement http://www.ebi.ac.uk/efo/EFO_0021978 GCST90242487 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein MENT levels (MENT.5744.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein MENT measurement http://www.ebi.ac.uk/efo/EFO_0801952 GCST90242488 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein MRVI1 levels (MRVI1.8255.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein MRVI1 measurement http://www.ebi.ac.uk/efo/EFO_0801953 GCST90242489 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein NDNF levels (NDNF.6604.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein NDNF measurement http://www.ebi.ac.uk/efo/EFO_0802953 GCST90242490 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein NDRG4 levels (NDRG4.7934.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein NDRG4 measurement http://www.ebi.ac.uk/efo/EFO_0801954 GCST90242491 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein NOV homolog levels (NOV.2737.22.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein nov homolog measurement http://www.ebi.ac.uk/efo/EFO_0020685 GCST90242492 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein O-glucosyltransferase 1 levels (POGLUT1.6467.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein O-glucosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801955 GCST90242493 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 levels (POMGNT1.8253.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802954 GCST90242494 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2 levels (POMGNT2.6359.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801956 GCST90242495 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein p13 MTCP-1 levels (MTCP1.12916.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein p13 MTCP-1 measurement http://www.ebi.ac.uk/efo/EFO_0802955 GCST90242496 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein phosphatase 1 regulatory subunit 3B levels (PPP1R3B.12768.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein phosphatase 1 regulatory subunit 3B measurement http://www.ebi.ac.uk/efo/EFO_0802956 GCST90242497 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein phosphatase 1A levels (PPM1A.12619.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein phosphatase 1A measurement http://www.ebi.ac.uk/efo/EFO_0802957 GCST90242498 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein phosphatase 1L levels (PPM1L.7187.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein phosphatase 1L measurement http://www.ebi.ac.uk/efo/EFO_0802958 GCST90242499 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein regulator of cytokinesis 1 levels (PRC1.11591.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein regulator of cytokinesis 1 measurement http://www.ebi.ac.uk/efo/EFO_0802959 GCST90242500 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein RIC-3 levels (RIC3.11228.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 protein RIC-3 measurement http://www.ebi.ac.uk/efo/EFO_0801957 GCST90242501 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Protein RIC-3 levels (RIC3.7125.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 protein RIC-3 measurement http://www.ebi.ac.uk/efo/EFO_0801957 GCST90242502 Genome-wide genotyping array 2022-01-18 34957434 Haas ME 2021-12-01 Cell Genom www.ncbi.nlm.nih.gov/pubmed/34957434 Machine learning enables new insights into genetic contributions to liver fat accumulation. Liver fat 32,974 European ancestry individuals 7,479 European ancestry individuals Affymetrix [9802892] (imputed) 2 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90029073 Genome-wide genotyping array 2022-05-16 35199045 Gehlen J 2022-01-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35199045 First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B. Esophageal atresia with or without tracheoesophageal fistula 764 European ancestry cases, 5,778 European ancestry controls NA Illumina [9140693] (imputed) 3 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90102511 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apoptosis-inducing factor 1, mitochondrial levels (AIFM1.9522.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 apoptosis-inducing factor 1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801389 GCST90240322 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Apoptotic protease-activating factor 1 levels (APAF1.13583.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 apoptotic protease-activating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801390 GCST90240323 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Appetite-regulating hormone levels (GHRL.8447.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 appetite-regulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0022016 GCST90240324 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium/calmodulin-dependent protein kinase type II subunit alpha levels (CAMK2A.3350.53.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 calcium/calmodulin-dependent protein kinase type II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020218 GCST90240557 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcium/calmodulin-dependent protein kinase type II subunit beta levels (CAMK2B.3351.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 calcium/calmodulin-dependent protein kinase type II subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020219 GCST90240558 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcyclin-binding protein levels (CACYBP.12432.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 calcyclin-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801443 GCST90240559 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calcyphosin-like protein levels (CAPSL.13688.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calcyphosin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802360 GCST90240560 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calnexin levels (CANX.8834.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 calnexin measurement http://www.ebi.ac.uk/efo/EFO_0801444 GCST90240561 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calpain-2 catalytic subunit levels (CAPN2.14684.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 calpain-2 catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0801445 GCST90240562 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calpain-3 levels (CAPN3.12385.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calpain-3 measurement http://www.ebi.ac.uk/efo/EFO_0802361 GCST90240563 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calpastatin levels (CAST.3026.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 calpastatin measurement http://www.ebi.ac.uk/efo/EFO_0008065 GCST90240564 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calreticulin levels (CALR.5264.65.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calreticulin measurement http://www.ebi.ac.uk/efo/EFO_0020221 GCST90240565 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calsenilin levels (KCNIP3.10513.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calsenilin measurement http://www.ebi.ac.uk/efo/EFO_0802362 GCST90240566 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Calsyntenin-3 levels (CLSTN3.6291.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 calsyntenin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802363 GCST90240567 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cAMP-dependent protein kinase catalytic subunit alpha levels (PRKACA.3466.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cAMP-dependent protein kinase catalytic subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020222 GCST90240568 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cAMP-dependent protein kinase type I-beta regulatory subunit levels (PRKAR1B.12479.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cAMP-dependent protein kinase type I-beta regulatory subunit measurement http://www.ebi.ac.uk/efo/EFO_0801446 GCST90240569 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cAMP-regulated phosphoprotein 19 levels (ARPP19.4963.19.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cAMP-regulated phosphoprotein 19 measurement http://www.ebi.ac.uk/efo/EFO_0020223 GCST90240570 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cAMP-regulated phosphoprotein 21 levels (ARPP21.12860.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cAMP-regulated phosphoprotein 21 measurement http://www.ebi.ac.uk/efo/EFO_0802364 GCST90240571 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. cAMP-specific 3',5'-cyclic phosphodiesterase 4D levels (PDE4D.5255.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 cAMP-specific 3',5'-cyclic phosphodiesterase 4D measurement http://www.ebi.ac.uk/efo/EFO_0020224 GCST90240572 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cancer/testis antigen 55 levels (CT55.9363.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cancer/testis antigen 55 measurement http://www.ebi.ac.uk/efo/EFO_0802365 GCST90240573 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 1 levels (CHST1.7803.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 carbohydrate sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801447 GCST90240574 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 11 levels (CHST11.7779.86.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 carbohydrate sulfotransferase 11 measurement http://www.ebi.ac.uk/efo/EFO_0801448 GCST90240575 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 14 levels (CHST14.7262.191.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbohydrate sulfotransferase 14 measurement http://www.ebi.ac.uk/efo/EFO_0802366 GCST90240576 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 15 levels (CHST15.4469.78.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90240577 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 15 levels (CHST15.14097.86.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90240578 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin Z levels (CTSZ.4971.1.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 cathepsin Z measurement http://www.ebi.ac.uk/efo/EFO_0008074 GCST90240629 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cation-dependent mannose-6-phosphate receptor levels (M6PR.10491.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cation-dependent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0801459 GCST90240630 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cation-independent mannose-6-phosphate receptor levels (IGF2R.3676.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90240631 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Caveolin-2 levels (CAV2.9457.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 caveolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802376 GCST90240632 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CCAAT/enhancer-binding protein beta levels (CEBPB.10337.83.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CCAAT/enhancer-binding protein beta measurement http://www.ebi.ac.uk/efo/EFO_0021905 GCST90240633 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CCR4-NOT transcription complex subunit 1 levels (CNOT1.13482.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CCR4-NOT transcription complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0802377 GCST90240634 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD109 antigen levels (CD109.3290.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CD109 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008076 GCST90240635 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD166 antigen levels (ALCAM.5451.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CD166 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020245 GCST90240636 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD177 antigen levels (CD177.13116.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 8 cD177 antigen measurement http://www.ebi.ac.uk/efo/EFO_0021866 GCST90240637 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD209 antigen levels (CD209.3029.52.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90240638 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD226 antigen levels (CD226.5721.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CD226 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020246 GCST90240639 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD226 antigen levels (CD226.5062.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CD226 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020246 GCST90240640 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD40 ligand levels (CD40LG.3534.14.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST90240641 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD44 antigen levels (CD44.9283.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CD44 antigen measurement http://www.ebi.ac.uk/efo/EFO_0802378 GCST90240642 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD48 antigen levels (CD48.3292.75.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CD48 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020247 GCST90240643 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD59 glycoprotein levels (CD59.11514.196.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CD59 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0021924 GCST90240644 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD63 antigen levels (CD63.9190.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 CD63 antigen measurement http://www.ebi.ac.uk/efo/EFO_0022033 GCST90240645 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD70 antigen levels (CD70.5807.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CD70 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020249 GCST90240646 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD70 antigen levels (CD70.8762.38.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CD70 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020249 GCST90240647 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CD97 antigen levels (CD97.2822.56.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CD97 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020250 GCST90240648 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CDGSH iron-sulfur domain-containing protein 1 levels (CISD1.7745.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 CDGSH iron-sulfur domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801460 GCST90240649 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. CDGSH iron-sulfur domain-containing protein 2 levels (CISD2.8094.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 CDGSH iron-sulfur domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802379 GCST90240650 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell adhesion molecule 1 levels (CADM1.3326.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0020251 GCST90240651 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell adhesion molecule 3 levels (CADM3.3630.27.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020252 GCST90240652 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell adhesion molecule 4 levels (CADM4.8619.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell adhesion molecule 4 measurement http://www.ebi.ac.uk/efo/EFO_0802380 GCST90240653 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell adhesion molecule-related/down-regulated by oncogenes levels (CDON.4541.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cell adhesion molecule-related/down-regulated by oncogenes measurement http://www.ebi.ac.uk/efo/EFO_0008079 GCST90240654 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Collagen alpha-1(VI) chain levels (COL6A1.11150.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 collagen alpha-1(VI) chain measurement http://www.ebi.ac.uk/efo/EFO_0801487 GCST90240745 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Deoxycytidine kinase levels (DCK.9836.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 deoxycytidine kinase measurement http://www.ebi.ac.uk/efo/EFO_0801523 GCST90240886 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Deoxynucleoside triphosphate triphosphohydrolase SAMHD1 levels (SAMHD1.11303.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 deoxynucleoside triphosphate triphosphohydrolase SAMHD1 measurement http://www.ebi.ac.uk/efo/EFO_0802459 GCST90240887 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Deoxyribonuclease-2-beta levels (DNASE2B.6533.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 deoxyribonuclease-2-beta measurement http://www.ebi.ac.uk/efo/EFO_0802460 GCST90240888 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Derlin-1 levels (DERL1.13393.46.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 derlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802461 GCST90240889 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dermatopontin levels (DPT.4979.34.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90240890 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dermokine levels (DMKN.8535.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dermokine measurement http://www.ebi.ac.uk/efo/EFO_0802462 GCST90240891 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Desert hedgehog protein N-product levels (DHH.4389.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 desert hedgehog protein n-product measurement http://www.ebi.ac.uk/efo/EFO_0020319 GCST90240892 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Desmin levels (DES.12030.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 desmin measurement http://www.ebi.ac.uk/efo/EFO_0802463 GCST90240893 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Desmocollin-2 levels (DSC2.13126.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 desmocollin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021936 GCST90240894 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Desmocollin-3 levels (DSC3.4981.6.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 desmocollin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020320 GCST90240895 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Desmoglein-1 levels (DSG1.2976.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 desmoglein-1 measurement http://www.ebi.ac.uk/efo/EFO_0020321 GCST90240896 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Desmoglein-2 levels (DSG2.9484.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 desmoglein-2 measurement http://www.ebi.ac.uk/efo/EFO_0020322 GCST90240897 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Di-N-acetylchitobiase levels (CTBS.6115.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 di-N-acetylchitobiase measurement http://www.ebi.ac.uk/efo/EFO_0801524 GCST90240898 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Diablo homolog, mitochondrial levels (DIABLO.3122.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 diablo homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020323 GCST90240899 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Diacylglycerol kinase beta levels (DGKB.12895.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 diacylglycerol kinase beta measurement http://www.ebi.ac.uk/efo/EFO_0801525 GCST90240900 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Diamine acetyltransferase 1 levels (SAT1.9859.180.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 diamine acetyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802464 GCST90240901 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Diamine acetyltransferase 2 levels (SAT2.12524.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 diamine acetyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802465 GCST90240902 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dickkopf-like protein 1 levels (DKKL1.3644.5.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 dickkopf-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020324 GCST90240903 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dickkopf-related protein 1 levels (DKK1.3535.84.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90240904 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dickkopf-related protein 3 levels (DKK3.3607.71.6) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90240905 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dickkopf-related protein 4 levels (DKK4.3365.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 Dickkopf-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008110 GCST90240906 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dihydrofolate reductase levels (DHFR.9823.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dihydrofolate reductase measurement http://www.ebi.ac.uk/efo/EFO_0801526 GCST90240907 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dihydrolipoyl dehydrogenase, mitochondrial levels (DLD.10025.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dihydrolipoyl dehydrogenase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802466 GCST90240908 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dihydropteridine reductase levels (QDPR.11257.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dihydropteridine reductase measurement http://www.ebi.ac.uk/efo/EFO_0801527 GCST90240909 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dihydropyrimidinase-related protein 3 levels (DPYSL3.12707.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dihydropyrimidinase-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802467 GCST90240910 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dihydropyrimidinase-related protein 5 levels (DPYSL5.12683.156.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dihydropyrimidinase-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802468 GCST90240911 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dipeptidase 1 levels (DPEP1.8794.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dipeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802469 GCST90240912 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dipeptidase 2 levels (DPEP2.8327.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 dipeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801528 GCST90240913 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dipeptidyl peptidase 1 levels (CTSC.3178.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dipeptidyl peptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020325 GCST90240914 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dipeptidyl peptidase 2 levels (DPP7.8346.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90240915 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Dipeptidyl peptidase 2 levels (DPP7.3608.12.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90240916 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Discoidin domain-containing receptor 2 levels (DDR2.3606.2.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 discoidin domain-containing receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020327 GCST90240917 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Discoidin, CUB and LCCL domain-containing protein 2 levels (DCBLD2.9338.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 discoidin, CUB and LCCL domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803294 GCST90240918 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Disintegrin and metalloproteinase domain-containing protein 11 levels (ADAM11.6586.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 disintegrin and metalloproteinase domain-containing protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0801529 GCST90240919 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Disintegrin and metalloproteinase domain-containing protein 12 levels (ADAM12.4420.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 disintegrin and metalloproteinase domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0020328 GCST90240920 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Disintegrin and metalloproteinase domain-containing protein 19 levels (ADAM19.8948.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 disintegrin and metalloproteinase domain-containing protein 19 measurement http://www.ebi.ac.uk/efo/EFO_0802470 GCST90240921 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Disintegrin and metalloproteinase domain-containing protein 23 levels (ADAM23.7049.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 disintegrin and metalloproteinase domain-containing protein 23 measurement http://www.ebi.ac.uk/efo/EFO_0801530 GCST90240922 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Disintegrin and metalloproteinase domain-containing protein 29 levels (ADAM29.13549.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 disintegrin and metalloproteinase domain-containing protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0802471 GCST90240923 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Disintegrin and metalloproteinase domain-containing protein 9 levels (ADAM9.3795.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 disintegrin and metalloproteinase domain-containing protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0020329 GCST90240924 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Disks large homolog 3 levels (DLG3.7897.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 disks large homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0802472 GCST90240925 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA dC->dU-editing enzyme APOBEC-3G levels (APOBEC3G.13930.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA dC->dU-editing enzyme APOBEC-3G measurement http://www.ebi.ac.uk/efo/EFO_0802473 GCST90240926 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA excision repair protein ERCC-1 levels (ERCC1.12585.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA excision repair protein ERCC-1 measurement http://www.ebi.ac.uk/efo/EFO_0802474 GCST90240927 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA polymerase eta levels (POLH.10022.207.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA polymerase eta measurement http://www.ebi.ac.uk/efo/EFO_0802475 GCST90240928 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA polymerase iota levels (POLI.13536.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA polymerase iota measurement http://www.ebi.ac.uk/efo/EFO_0802476 GCST90240929 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA primase small subunit levels (PRIM1.13591.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA primase small subunit measurement http://www.ebi.ac.uk/efo/EFO_0802477 GCST90240930 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA repair endonuclease XPF levels (ERCC4.9895.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 DNA repair endonuclease XPF measurement http://www.ebi.ac.uk/efo/EFO_0802478 GCST90240931 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA repair protein RAD51 homolog 1 levels (RAD51.2871.73.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 DNA repair protein rad51 homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0020330 GCST90240932 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. DNA repair protein RAD51 homolog 4 levels (RAD51L3.12554.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 DNA repair protein RAD51 homolog 4 measurement http://www.ebi.ac.uk/efo/EFO_0801531 GCST90240933 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 2 levels (CHST2.4428.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbohydrate sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020225 GCST90240579 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 3 levels (CHST3.7189.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbohydrate sulfotransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802367 GCST90240580 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 5 levels (CHST5.7020.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbohydrate sulfotransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0802368 GCST90240581 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 6 levels (CHST6.4429.51.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbohydrate sulfotransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020226 GCST90240582 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbohydrate sulfotransferase 9 levels (CHST9.11646.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 carbohydrate sulfotransferase 9 measurement http://www.ebi.ac.uk/efo/EFO_0801449 GCST90240583 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase 1 levels (CA1.4969.2.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbonic anhydrase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020227 GCST90240584 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase 2 levels (CA2.4970.55.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbonic anhydrase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020228 GCST90240585 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase 3 levels (CA3.3799.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 carbonic anhydrase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020229 GCST90240586 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase 4 levels (CA4.3177.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 carbonic anhydrase 4 measurement http://www.ebi.ac.uk/efo/EFO_0020230 GCST90240587 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase 5A, mitochondrial levels (CA5A.8791.151.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 carbonic anhydrase 5A, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801450 GCST90240588 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase 6 levels (CA6.3352.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 carbonic anhydrase 6 measurement http://www.ebi.ac.uk/efo/EFO_0008068 GCST90240589 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase 9 levels (CA9.3798.71.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbonic anhydrase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020232 GCST90240590 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase-related protein 10 levels (CA10.13666.222.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 carbonic anhydrase-related protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020233 GCST90240591 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonic anhydrase-related protein 10 levels (CA10.3289.19.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carbonic anhydrase-related protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020233 GCST90240592 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonyl reductase [NADPH] 1 levels (CBR1.12381.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 carbonyl reductase [NADPH] 1 measurement http://www.ebi.ac.uk/efo/EFO_0803310 GCST90240593 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carbonyl reductase [NADPH] 3 levels (CBR3.14091.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 carbonyl reductase [NADPH] 3 measurement http://www.ebi.ac.uk/efo/EFO_0803315 GCST90240594 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carboxypeptidase A2 levels (CPA2.9276.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 carboxypeptidase A2 measurement http://www.ebi.ac.uk/efo/EFO_0801451 GCST90240595 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carboxypeptidase A4 levels (CPA4.9267.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 carboxypeptidase A4 measurement http://www.ebi.ac.uk/efo/EFO_0801452 GCST90240596 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carboxypeptidase B levels (CPB1.6356.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 carboxypeptidase B measurement http://www.ebi.ac.uk/efo/EFO_0801453 GCST90240597 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carboxypeptidase M levels (CPM.7768.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 carboxypeptidase M measurement http://www.ebi.ac.uk/efo/EFO_0801454 GCST90240598 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carboxypeptidase Z levels (CPZ.6493.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 carboxypeptidase Z measurement http://www.ebi.ac.uk/efo/EFO_0801455 GCST90240599 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carcinoembryonic antigen-related cell adhesion molecule 1 levels (CEACAM1.8031.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 carcinoembryonic antigen-related cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0801456 GCST90240600 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carcinoembryonic antigen-related cell adhesion molecule 21 levels (CEACAM21.7204.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carcinoembryonic antigen-related cell adhesion molecule 21 measurement http://www.ebi.ac.uk/efo/EFO_0802369 GCST90240601 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Carcinoembryonic antigen-related cell adhesion molecule 4 levels (CEACAM4.10910.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 carcinoembryonic antigen-related cell adhesion molecule 4 measurement http://www.ebi.ac.uk/efo/EFO_0802370 GCST90240602 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cardiotrophin-1 levels (CTF1.13732.79.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cardiotrophin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020235 GCST90240603 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cardiotrophin-1 levels (CTF1.2889.37.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cardiotrophin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020235 GCST90240604 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cartilage intermediate layer protein 1 levels (CILP.5717.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cartilage intermediate layer protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801457 GCST90240605 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cas scaffolding protein family member 4 levels (CASS4.12855.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cas scaffolding protein family member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802371 GCST90240606 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Casein kinase I isoform delta levels (CSNK1D.11289.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 casein kinase I isoform delta measurement http://www.ebi.ac.uk/efo/EFO_0802372 GCST90240607 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Casein kinase I isoform gamma-2 levels (CSNK1G2.12653.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 casein kinase I isoform gamma-2 measurement http://www.ebi.ac.uk/efo/EFO_0801458 GCST90240608 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Casein kinase II 2-alpha:2-beta heterotetramer levels (CSNK2A1.CSNK2B.5225.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 casein kinase II 2-alpha:2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020236 GCST90240609 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Casein kinase II 2-alpha':2-beta heterotetramer levels (CSNK2A2.CSNK2B.5226.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 casein kinase II 2-alpha':2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020237 GCST90240610 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Casein kinase II subunit alpha levels (CSNK2A1.3427.63.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 casein kinase II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020238 GCST90240611 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Casein kinase II subunit alpha levels (CSNK2A1.5224.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 casein kinase II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020238 GCST90240612 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Caseinolytic peptidase B protein homolog levels (CLPB.11860.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 caseinolytic peptidase B protein homolog measurement http://www.ebi.ac.uk/efo/EFO_0802373 GCST90240613 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Caspase-10 levels (CASP10.5340.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 caspase-10 measurement http://www.ebi.ac.uk/efo/EFO_0020239 GCST90240614 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Caspase-2 levels (CASP2.4904.7.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 caspase-2 measurement http://www.ebi.ac.uk/efo/EFO_0020240 GCST90240615 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Caspase-3 levels (CASP3.3593.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 caspase-3 measurement http://www.ebi.ac.uk/efo/EFO_0008070 GCST90240616 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Catalase levels (CAT.3488.64.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 catalase measurement http://www.ebi.ac.uk/efo/EFO_0008071 GCST90240617 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Catenin alpha-2 levels (CTNNA2.9872.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 catenin alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0802374 GCST90240618 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin B levels (CTSB.3061.61.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90240619 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin E levels (CTSE.3594.6.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cathepsin E measurement http://www.ebi.ac.uk/efo/EFO_0020241 GCST90240620 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin F levels (CTSF.9212.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cathepsin F measurement http://www.ebi.ac.uk/efo/EFO_0022038 GCST90240621 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin F levels (CTSF.8393.121.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cathepsin F measurement http://www.ebi.ac.uk/efo/EFO_0022038 GCST90240622 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin G levels (CTSG.2431.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cathepsin G measurement http://www.ebi.ac.uk/efo/EFO_0020242 GCST90240623 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin H levels (CTSH.8465.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90240624 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin H levels (CTSH.3737.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90240625 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin L2 levels (CTSV.3364.76.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cathepsin L2 measurement http://www.ebi.ac.uk/efo/EFO_0020244 GCST90240626 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin O levels (CTSO.9264.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cathepsin O measurement http://www.ebi.ac.uk/efo/EFO_0802375 GCST90240627 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cathepsin S levels (CTSS.3181.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90240628 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poly [ADP-ribose] polymerase 1 levels (PARP1.10534.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 poly [ADP-ribose] polymerase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802876 GCST90242303 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poly [ADP-ribose] polymerase 11 levels (PARP11.12882.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 poly [ADP-ribose] polymerase 11 measurement http://www.ebi.ac.uk/efo/EFO_0802877 GCST90242304 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poly(A) polymerase gamma levels (PAPOLG.8343.224.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 poly(A) polymerase gamma measurement http://www.ebi.ac.uk/efo/EFO_0802878 GCST90242305 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poly(A) RNA polymerase, mitochondrial levels (MTPAP.9028.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 poly(A) RNA polymerase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801893 GCST90242306 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poly(rC)-binding protein 1 levels (PCBP1.11458.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 poly(rC)-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801894 GCST90242307 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poly(U)-binding-splicing factor PUF60 levels (PUF60.10575.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 poly(U)-binding-splicing factor PUF60 measurement http://www.ebi.ac.uk/efo/EFO_0801895 GCST90242308 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poly(U)-specific endoribonuclease levels (ENDOU.5656.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 poly(U)-specific endoribonuclease measurement http://www.ebi.ac.uk/efo/EFO_0802879 GCST90242309 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polyadenylate-binding protein 3 levels (PABPC3.10447.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 polyadenylate-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801896 GCST90242310 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polyadenylate-binding protein 4 levels (PABPC4.12603.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 polyadenylate-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801897 GCST90242311 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polyadenylate-binding protein-interacting protein 1 levels (PAIP1.12430.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polyadenylate-binding protein-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802880 GCST90242312 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polycomb protein SCMH1 levels (SCMH1.12604.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 polycomb protein SCMH1 measurement http://www.ebi.ac.uk/efo/EFO_0801898 GCST90242313 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polycystin-2 levels (PKD2.13745.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polycystin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802881 GCST90242314 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polymeric immunoglobulin receptor levels (PIGR.3216.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90242315 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polypeptide N-acetylgalactosaminyltransferase 1 levels (GALNT1.7090.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 polypeptide N-acetylgalactosaminyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801899 GCST90242316 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polypeptide N-acetylgalactosaminyltransferase 10 levels (GALNT10.7003.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polypeptide N-acetylgalactosaminyltransferase 10 measurement http://www.ebi.ac.uk/efo/EFO_0802882 GCST90242317 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polypeptide N-acetylgalactosaminyltransferase 11 levels (GALNT11.8700.325.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polypeptide N-acetylgalactosaminyltransferase 11 measurement http://www.ebi.ac.uk/efo/EFO_0802883 GCST90242318 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polypeptide N-acetylgalactosaminyltransferase 16 levels (GALNT16.8923.94.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 polypeptide N-acetylgalactosaminyltransferase 16 measurement http://www.ebi.ac.uk/efo/EFO_0801900 GCST90242319 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polypeptide N-acetylgalactosaminyltransferase 2 levels (GALNT2.5764.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polypeptide N-acetylgalactosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802884 GCST90242320 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polypeptide N-acetylgalactosaminyltransferase 3 levels (GALNT3.6593.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polypeptide N-acetylgalactosaminyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802885 GCST90242321 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Polyphosphoinositide phosphatase levels (FIG4.6948.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polyphosphoinositide phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0802886 GCST90242322 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PolyUbiquitin K48-linked levels (UBB.6651.74.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 polyUbiquitin K48-linked measurement http://www.ebi.ac.uk/efo/EFO_0022007 GCST90242323 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PolyUbiquitin K48-linked levels (UBB.6641.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polyUbiquitin K48-linked measurement http://www.ebi.ac.uk/efo/EFO_0022007 GCST90242324 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PolyUbiquitin K63-linked levels (UBC.6647.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 polyUbiquitin K63-linked measurement http://www.ebi.ac.uk/efo/EFO_0022008 GCST90242325 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Porphobilinogen deaminase levels (HMBS.11530.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 porphobilinogen deaminase measurement http://www.ebi.ac.uk/efo/EFO_0802887 GCST90242326 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Potassium voltage-gated channel subfamily A member 10 levels (KCNA10.13042.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 potassium voltage-gated channel subfamily A member 10 measurement http://www.ebi.ac.uk/efo/EFO_0802888 GCST90242327 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Osteomodulin levels (OMD.5358.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 osteomodulin measurement http://www.ebi.ac.uk/efo/EFO_0020619 GCST90242178 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Out at first protein homolog levels (OAF.6414.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 out at first protein homolog measurement http://www.ebi.ac.uk/efo/EFO_0801862 GCST90242179 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. OX-2 membrane glycoprotein levels (CD200.5112.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 OX-2 membrane glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008253 GCST90242180 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oxidized low-density lipoprotein receptor 1 levels (OLR1.3636.37.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 oxidized low-density lipoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020620 GCST90242181 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oxidoreductase HTATIP2 levels (HTATIP2.7753.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 oxidoreductase HTATIP2 measurement http://www.ebi.ac.uk/efo/EFO_0801863 GCST90242182 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oxidoreductase HTATIP2 levels (HTATIP2.10630.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 oxidoreductase HTATIP2 measurement http://www.ebi.ac.uk/efo/EFO_0801863 GCST90242183 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oxysterol-binding protein-related protein 11 levels (OSBPL11.12878.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 oxysterol-binding protein-related protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0801864 GCST90242184 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oxysterols receptor LXR-beta levels (NR1H2.9016.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 oxysterols receptor LXR-beta measurement http://www.ebi.ac.uk/efo/EFO_0801865 GCST90242185 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oxytocin-neurophysin 1 levels (OXT.8257.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 oxytocin-neurophysin 1 measurement http://www.ebi.ac.uk/efo/EFO_0802839 GCST90242186 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. P-selectin levels (SELP.4154.57.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90242187 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. P-selectin glycoprotein ligand 1 levels (SELPLG.11266.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 P-selectin glycoprotein ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0010922 GCST90242188 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. P2X purinoceptor 6 levels (P2RX6.7233.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 P2X purinoceptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0802840 GCST90242189 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. p53 and DNA damage-regulated protein 1 levels (PDRG1.12593.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 p53 and DNA damage-regulated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803313 GCST90242190 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Paired box protein Pax-4 levels (PAX4.12398.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 paired box protein Pax-4 measurement http://www.ebi.ac.uk/efo/EFO_0802841 GCST90242191 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Paired immunoglobulin-like type 2 receptor alpha levels (PILRA.8683.119.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 paired immunoglobulin-like type 2 receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0801866 GCST90242192 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Paired immunoglobulin-like type 2 receptor alpha levels (PILRA.8825.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 paired immunoglobulin-like type 2 receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0801866 GCST90242193 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Palmitoleoyl-protein carboxylesterase NOTUM levels (NOTUM.8252.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 palmitoleoyl-protein carboxylesterase NOTUM measurement http://www.ebi.ac.uk/efo/EFO_0802842 GCST90242194 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Palmitoyl-protein thioesterase 1 levels (PPT1.9244.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 palmitoyl-protein thioesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801867 GCST90242195 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pancreatic hormone levels (PPY.4588.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 pancreatic hormone measurement http://www.ebi.ac.uk/efo/EFO_0020621 GCST90242196 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pantothenate kinase 3 levels (PANK3.12658.72.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pantothenate kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802843 GCST90242197 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Papilin levels (PAPLN.11254.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 papilin measurement http://www.ebi.ac.uk/efo/EFO_0802844 GCST90242198 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pappalysin-1 levels (PAPPA.4148.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pappalysin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802845 GCST90242199 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pappalysin-2 levels (PAPPA2.5756.66.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pappalysin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802846 GCST90242200 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Parathyroid hormone levels (PTH.5954.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST90242201 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Parathyroid hormone-related protein levels (PTHLH.2962.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 parathyroid hormone-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020622 GCST90242202 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Periostin levels (POSTN.6645.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90242228 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxidasin-like protein levels (PXDNL.11324.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peroxidasin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802854 GCST90242229 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxiredoxin-1 levels (PRDX1.3855.56.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peroxiredoxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020629 GCST90242230 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxiredoxin-4 levels (PRDX4.7789.182.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peroxiredoxin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802855 GCST90242231 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxisomal carnitine O-octanoyltransferase levels (CROT.13929.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peroxisomal carnitine O-octanoyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802856 GCST90242232 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxisomal membrane protein PEX14 levels (PEX14.8300.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peroxisomal membrane protein PEX14 measurement http://www.ebi.ac.uk/efo/EFO_0802857 GCST90242233 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxisomal NADH pyrophosphatase NUDT12 levels (NUDT12.13947.371.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peroxisomal NADH pyrophosphatase NUDT12 measurement http://www.ebi.ac.uk/efo/EFO_0801878 GCST90242234 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxisomal targeting signal 1 receptor levels (PEX5.5915.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peroxisomal targeting signal 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0022001 GCST90242235 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peroxisome proliferator-activated receptor alpha levels (PPARA.12954.71.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peroxisome proliferator-activated receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0802858 GCST90242236 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Persephin levels (PSPN.2696.87.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 persephin measurement http://www.ebi.ac.uk/efo/EFO_0020632 GCST90242237 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Persulfide dioxygenase ETHE1, mitochondrial levels (ETHE1.3847.56.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 persulfide dioxygenase ETHE1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008258 GCST90242238 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pescadillo homolog levels (PES1.4267.81.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pescadillo homolog measurement http://www.ebi.ac.uk/efo/EFO_0020633 GCST90242239 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PH and SEC7 domain-containing protein 1 levels (PSD.13055.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 PH and SEC7 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803302 GCST90242240 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PH and SEC7 domain-containing protein 2 levels (PSD2.9118.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 PH and SEC7 domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803295 GCST90242241 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PHD finger protein 3 levels (PHF3.11544.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 PHD finger protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802859 GCST90242242 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phenylalanine--tRNA ligase, mitochondrial levels (FARS2.13941.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 phenylalanine--tRNA ligase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801879 GCST90242243 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosducin-like protein 2 levels (PDCL2.14192.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 phosducin-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801880 GCST90242244 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidate phosphatase PPAPDC1A levels (PPAPDC1A.13548.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphatidate phosphatase PPAPDC1A measurement http://www.ebi.ac.uk/efo/EFO_0802860 GCST90242245 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN levels (PTEN.3831.21.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase pten measurement http://www.ebi.ac.uk/efo/EFO_0020635 GCST90242246 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha levels (PIK3C2A.14028.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801881 GCST90242247 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform levels (PIK3CG.3391.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform measurement http://www.ebi.ac.uk/efo/EFO_0020637 GCST90242248 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha levels (PIP4K2A.12697.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphatidylinositol 5-phosphate 4-kinase type-2 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802861 GCST90242249 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol transfer protein alpha isoform levels (PITPNA.9934.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphatidylinositol transfer protein alpha isoform measurement http://www.ebi.ac.uk/efo/EFO_0802862 GCST90242250 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol transfer protein beta isoform levels (PITPNB.12484.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphatidylinositol transfer protein beta isoform measurement http://www.ebi.ac.uk/efo/EFO_0802863 GCST90242251 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol-glycan-specific phospholipase D levels (GPLD1.11939.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 phosphatidylinositol-glycan-specific phospholipase D measurement http://www.ebi.ac.uk/efo/EFO_0801882 GCST90242252 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Parathyroid hormone/parathyroid hormone-related peptide receptor levels (PTH1R.13470.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 parathyroid hormone/parathyroid hormone-related peptide receptor measurement http://www.ebi.ac.uk/efo/EFO_0802847 GCST90242203 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Patched domain-containing protein 3 levels (PTCHD3.13517.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 patched domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802848 GCST90242204 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PAX-interacting protein 1 levels (PAXIP1.12894.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 PAX-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801868 GCST90242205 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PDZ and LIM domain protein 4 levels (PDLIM4.12387.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 PDZ and LIM domain protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802849 GCST90242206 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PDZ domain-containing protein 11 levels (PDZD11.6219.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 PDZ domain-containing protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0802850 GCST90242207 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PDZK1-interacting protein 1 levels (PDZK1IP1.8260.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 PDZK1-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801869 GCST90242208 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pentraxin-related protein PTX3 levels (PTX3.6447.73.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pentraxin-related protein PTX3 measurement http://www.ebi.ac.uk/efo/EFO_0010923 GCST90242209 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidase inhibitor 15 levels (PI15.5745.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peptidase inhibitor 15 measurement http://www.ebi.ac.uk/efo/EFO_0802851 GCST90242210 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptide chain release factor 1-like, mitochondrial levels (MTRF1L.11134.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptide chain release factor 1-like, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801870 GCST90242211 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptide YY levels (PYY.3727.35.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peptide yy measurement http://www.ebi.ac.uk/efo/EFO_0020623 GCST90242212 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidoglycan recognition protein 1 levels (PGLYRP1.3329.14.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90242213 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-glycine alpha-amidating monooxygenase levels (PAM.5620.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 peptidyl-glycine alpha-amidating monooxygenase measurement http://www.ebi.ac.uk/efo/EFO_0801871 GCST90242214 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase A levels (PPIA.5247.17.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidyl-prolyl cis-trans isomerase A measurement http://www.ebi.ac.uk/efo/EFO_0020625 GCST90242215 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase B levels (PPIB.4718.5.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peptidyl-prolyl cis-trans isomerase B measurement http://www.ebi.ac.uk/efo/EFO_0020626 GCST90242216 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase E levels (PPIE.5238.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidyl-prolyl cis-trans isomerase E measurement http://www.ebi.ac.uk/efo/EFO_0008257 GCST90242217 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase FKBP14 levels (FKBP14.9340.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidyl-prolyl cis-trans isomerase FKBP14 measurement http://www.ebi.ac.uk/efo/EFO_0801872 GCST90242218 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase FKBP2 levels (FKBP2.9339.204.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peptidyl-prolyl cis-trans isomerase FKBP2 measurement http://www.ebi.ac.uk/efo/EFO_0802852 GCST90242219 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase FKBP7 levels (FKBP7.9288.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidyl-prolyl cis-trans isomerase FKBP7 measurement http://www.ebi.ac.uk/efo/EFO_0801873 GCST90242220 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase H levels (PPIH.12449.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidyl-prolyl cis-trans isomerase H measurement http://www.ebi.ac.uk/efo/EFO_0801874 GCST90242221 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase NIMA-interacting 4 levels (PIN4.12718.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidyl-prolyl cis-trans isomerase NIMA-interacting 4 measurement http://www.ebi.ac.uk/efo/EFO_0801875 GCST90242222 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase-like 1 levels (PPIL1.9884.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 peptidyl-prolyl cis-trans isomerase-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801876 GCST90242223 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peptidyl-prolyl cis-trans isomerase-like 2 levels (PPIL2.14314.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 peptidyl-prolyl cis-trans isomerase-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801877 GCST90242224 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Peregrin levels (BRPF1.11671.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 peregrin measurement http://www.ebi.ac.uk/efo/EFO_0802853 GCST90242225 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Periostin levels (POSTN.6650.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90242226 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Periostin levels (POSTN.3457.57.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90242227 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphatidylinositol-glycan-specific phospholipase D levels (GPLD1.9500.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphatidylinositol-glycan-specific phospholipase D measurement http://www.ebi.ac.uk/efo/EFO_0801882 GCST90242253 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphoglucomutase-1 levels (PGM1.9173.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 phosphoglucomutase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021859 GCST90242254 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphoglycerate kinase 1 levels (PGK1.5020.50.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 phosphoglycerate kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020638 GCST90242255 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphoglycerate kinase 2 levels (PGK2.13936.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphoglycerate kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802864 GCST90242256 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phospholipase A2, membrane associated levels (PLA2G2A.2692.74.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90242257 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phospholipase B-like 1 levels (PLBD1.6315.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phospholipase B-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0802865 GCST90242258 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phospholipase D3 levels (PLD3.10948.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phospholipase D3 measurement http://www.ebi.ac.uk/efo/EFO_0802866 GCST90242259 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphomevalonate kinase levels (PMVK.12450.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 phosphomevalonate kinase measurement http://www.ebi.ac.uk/efo/EFO_0801883 GCST90242260 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphopantothenoylcysteine decarboxylase levels (PPCDC.13996.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphopantothenoylcysteine decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0802867 GCST90242261 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Phosphoribosyl pyrophosphate synthase-associated protein 1 levels (PRPSAP1.9478.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 phosphoribosyl pyrophosphate synthase-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802868 GCST90242262 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pigment epithelium-derived factor levels (SERPINF1.9211.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 pigment epithelium-derived factor measurement http://www.ebi.ac.uk/efo/EFO_0021847 GCST90242263 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pigment epithelium-derived factor levels (SERPINF1.7735.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pigment epithelium-derived factor measurement http://www.ebi.ac.uk/efo/EFO_0021847 GCST90242264 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PIK3CA/PIK3R1 levels (PIK3CA.PIK3R1.3390.72.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 PIK3CA/PIK3R1 measurement http://www.ebi.ac.uk/efo/EFO_0021971 GCST90242265 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PILR alpha-associated neural protein levels (PIANP.9599.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 PILR alpha-associated neural protein measurement http://www.ebi.ac.uk/efo/EFO_0021941 GCST90242266 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. PILR alpha-associated neural protein levels (PIANP.14114.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 PILR alpha-associated neural protein measurement http://www.ebi.ac.uk/efo/EFO_0021941 GCST90242267 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pirin levels (PIR.13634.209.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 pirin measurement http://www.ebi.ac.uk/efo/EFO_0801884 GCST90242268 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pituitary adenylate cyclase-activating polypeptide levels (ADCYAP1.8285.64.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pituitary adenylate cyclase-activating polypeptide measurement http://www.ebi.ac.uk/efo/EFO_0802869 GCST90242269 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pituitary adenylate cyclase-activating polypeptide levels (ADCYAP1.4593.11.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pituitary adenylate cyclase-activating polypeptide measurement http://www.ebi.ac.uk/efo/EFO_0802869 GCST90242270 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pituitary adenylate cyclase-activating polypeptide levels (ADCYAP1.4594.22.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pituitary adenylate cyclase-activating polypeptide measurement http://www.ebi.ac.uk/efo/EFO_0802869 GCST90242271 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Piwi-like protein 1 levels (PIWIL1.12793.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 piwi-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802870 GCST90242272 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Placenta growth factor levels (PGF.3078.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 placenta growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010626 GCST90242273 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plasma protease C1 inhibitor levels (SERPING1.4479.14.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90242274 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plasmin levels (PLG.4150.75.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 plasmin measurement http://www.ebi.ac.uk/efo/EFO_0020643 GCST90242275 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plasminogen activator inhibitor 1 levels (SERPINE1.2925.9.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90242276 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plastin-1 levels (PLS1.12737.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 plastin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802871 GCST90242277 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plastin-2 levels (LCP1.9749.190.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 plastin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801885 GCST90242278 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet endothelial aggregation receptor 1 levels (PEAR1.8275.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 platelet endothelial aggregation receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801886 GCST90242279 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet endothelial aggregation receptor 1 levels (PEAR1.8892.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 platelet endothelial aggregation receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801886 GCST90242280 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet endothelial cell adhesion molecule levels (PECAM1.2695.25.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90242281 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet factor 4 variant levels (PF4V1.5663.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 platelet factor 4 variant measurement http://www.ebi.ac.uk/efo/EFO_0801887 GCST90242282 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet glycoprotein 4 levels (CD36.2973.15.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 platelet glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008262 GCST90242283 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet glycoprotein Ib alpha chain levels (GP1BA.4990.87.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 platelet glycoprotein ib alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0020645 GCST90242284 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet glycoprotein V levels (GP5.7185.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 platelet glycoprotein V measurement http://www.ebi.ac.uk/efo/EFO_0802872 GCST90242285 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet receptor Gi24 levels (C10orf54.14123.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 platelet receptor Gi24 measurement http://www.ebi.ac.uk/efo/EFO_0021877 GCST90242286 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-activating factor acetylhydrolase IB subunit beta levels (PAFAH1B2.2642.4.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 platelet-activating factor acetylhydrolase ib subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020646 GCST90242287 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-derived growth factor C levels (PDGFC.3828.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 platelet-derived growth factor c measurement http://www.ebi.ac.uk/efo/EFO_0020648 GCST90242288 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-derived growth factor D levels (PDGFD.9341.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 platelet-derived growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0801888 GCST90242289 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-derived growth factor receptor alpha levels (PDGFRA.10366.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 platelet-derived growth factor receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0021844 GCST90242290 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-derived growth factor receptor beta levels (PDGFRB.3459.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90242291 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-derived growth factor receptor-like protein levels (PDGFRL.9713.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 platelet-derived growth factor receptor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801889 GCST90242292 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-derived growth factor subunit A levels (PDGFA.4499.21.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 platelet-derived growth factor subunit A measurement http://www.ebi.ac.uk/efo/EFO_0801890 GCST90242293 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Platelet-derived growth factor subunit B levels (PDGFB.4149.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 platelet-derived growth factor subunit b measurement http://www.ebi.ac.uk/efo/EFO_0020650 GCST90242294 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pleckstrin homology domain-containing family A member 1 levels (PLEKHA1.12459.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 pleckstrin homology domain-containing family A member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802873 GCST90242295 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pleckstrin homology domain-containing family A member 7 levels (PLEKHA7.12731.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 pleckstrin homology domain-containing family A member 7 measurement http://www.ebi.ac.uk/efo/EFO_0801891 GCST90242296 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Pleiotrophin levels (PTN.3045.72.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 pleiotrophin measurement http://www.ebi.ac.uk/efo/EFO_0020651 GCST90242297 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plexin-A1 levels (PLXNA1.9005.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 plexin-A1 measurement http://www.ebi.ac.uk/efo/EFO_0801892 GCST90242298 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plexin-B2 levels (PLXNB2.9216.100.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 plexin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0021867 GCST90242299 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Plexin-C1 levels (PLXNC1.4564.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 plexin-C1 measurement http://www.ebi.ac.uk/efo/EFO_0008266 GCST90242300 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Podocalyxin levels (PODXL.8792.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 podocalyxin measurement http://www.ebi.ac.uk/efo/EFO_0802874 GCST90242301 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Poliovirus receptor levels (PVR.8064.125.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 poliovirus receptor measurement http://www.ebi.ac.uk/efo/EFO_0802875 GCST90242302 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Detectable estradiol levels 1,706 African ancestry cases, 3,630 African ancestry controls, 48,487 European ancestry cases, 181,479 European ancestry controls NA NR [NR] (imputed) 10 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90104295 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Testosterone levels 4,229 African ancestry individuals, 182,648 European ancestry individuals NA NR [NR] (imputed) 156 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90104296 Genome-wide genotyping array 2022-06-13 35192695 Haas CB 2022-02-22 Endocrinology www.ncbi.nlm.nih.gov/pubmed/35192695 Cross-ancestry genome-wide association studies of sex hormone concentrations in pre- and postmenopausal women. Sex hormone-binding globulin levels 4,522 African ancestry individuals, 196,901 European ancestry individuals NA NR [NR] (imputed) 288 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90104297 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Agouti-related protein levels (AGRP.2813.11.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90240217 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Agouti-signaling protein levels (ASIP.5676.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 Agouti-signaling protein measurement http://www.ebi.ac.uk/efo/EFO_0801357 GCST90240218 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alanine aminotransferase 1 levels (GPT.3709.4.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alanine aminotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802260 GCST90240219 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alanine--tRNA ligase, cytoplasmic levels (AARS.12340.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alanine--tRNA ligase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0801359 GCST90240220 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alcohol dehydrogenase [NADP(+)] levels (AKR1A1.4192.10.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 alcohol dehydrogenase [NADP(+)] measurement http://www.ebi.ac.uk/efo/EFO_0021977 GCST90240221 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alcohol dehydrogenase 1B levels (ADH1B.9834.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alcohol dehydrogenase 1B measurement http://www.ebi.ac.uk/efo/EFO_0801360 GCST90240222 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alcohol dehydrogenase 4 levels (ADH4.8325.37.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alcohol dehydrogenase 4 measurement http://www.ebi.ac.uk/efo/EFO_0802261 GCST90240223 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aldehyde dehydrogenase family 3 member B1 levels (ALDH3B1.12940.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 aldehyde dehydrogenase family 3 member B1 measurement http://www.ebi.ac.uk/efo/EFO_0801361 GCST90240224 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aldehyde dehydrogenase, dimeric NADP-preferring levels (ALDH3A1.11480.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 aldehyde dehydrogenase, dimeric NADP-preferring measurement http://www.ebi.ac.uk/efo/EFO_0801362 GCST90240225 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aldo-keto reductase family 1 member C1 levels (AKR1C1.12618.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 aldo-keto reductase family 1 member C1 measurement http://www.ebi.ac.uk/efo/EFO_0801363 GCST90240226 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aldose reductase levels (AKR1B1.9854.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 aldose reductase measurement http://www.ebi.ac.uk/efo/EFO_0801364 GCST90240227 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. All-trans-retinol 13,14-reductase levels (RETSAT.8381.18.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 all-trans-retinol 13,14-reductase measurement http://www.ebi.ac.uk/efo/EFO_0802262 GCST90240228 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Allergin-1 levels (MILR1.11173.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 allergin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801365 GCST90240229 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Allograft inflammatory factor 1 levels (AIF1.2849.49.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 allograft inflammatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020135 GCST90240230 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-(1,3)-fucosyltransferase 10 levels (FUT10.7156.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 alpha-(1,3)-fucosyltransferase 10 measurement http://www.ebi.ac.uk/efo/EFO_0801366 GCST90240231 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-(1,3)-fucosyltransferase 5 levels (FUT5.4549.78.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 alpha-(1,3)-fucosyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020136 GCST90240232 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-(1,3)-fucosyltransferase 9 levels (FUT9.6991.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 alpha-(1,3)-fucosyltransferase 9 measurement http://www.ebi.ac.uk/efo/EFO_0801367 GCST90240233 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-(1,6)-fucosyltransferase levels (FUT8.8244.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 alpha-(1,6)-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0801368 GCST90240234 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase levels (MGAT1.10571.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802263 GCST90240235 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B levels (MGAT4B.7141.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B measurement http://www.ebi.ac.uk/efo/EFO_0801369 GCST90240236 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C levels (MGAT4C.7208.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C measurement http://www.ebi.ac.uk/efo/EFO_0802264 GCST90240237 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase levels (MGAT2.6909.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0801370 GCST90240238 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-2-antiplasmin levels (SERPINF2.3024.18.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha-2-antiplasmin measurement http://www.ebi.ac.uk/efo/EFO_0020137 GCST90240239 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-2-HS-glycoprotein levels (AHSG.3581.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90240240 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. alpha-2-macroglobulin receptor-associated protein levels (LRPAP1.3640.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90240241 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-2-macroglobulin receptor-associated protein levels (LRPAP1.8829.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90240242 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-2,8-sialyltransferase 8B levels (ST8SIA2.7920.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-2,8-sialyltransferase 8B measurement http://www.ebi.ac.uk/efo/EFO_0802265 GCST90240243 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-2,8-sialyltransferase 8F levels (ST8SIA6.6930.95.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-2,8-sialyltransferase 8F measurement http://www.ebi.ac.uk/efo/EFO_0802266 GCST90240244 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-amylase 1 levels (AMY1A.7918.114.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 alpha-amylase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801371 GCST90240245 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-crystallin A chain levels (CRYAA.10087.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-crystallin A chain measurement http://www.ebi.ac.uk/efo/EFO_0802267 GCST90240246 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. alpha-Fetoprotein levels (AFP.5792.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST90240247 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-internexin levels (INA.11436.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-internexin measurement http://www.ebi.ac.uk/efo/EFO_0802268 GCST90240248 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-L-iduronidase levels (IDUA.3169.70.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 7 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90240249 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 levels (ST6GALNAC1.7867.154.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801372 GCST90240250 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 levels (ST6GALNAC2.7823.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801373 GCST90240251 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 levels (ST6GALNAC3.10626.116.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801374 GCST90240252 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 levels (ST6GALNAC3.10705.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801374 GCST90240253 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 levels (ST6GALNAC5.7927.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0802269 GCST90240254 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 levels (ST6GALNAC6.7228.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0802270 GCST90240255 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-parvin levels (PARVA.13434.172.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-parvin measurement http://www.ebi.ac.uk/efo/EFO_0802271 GCST90240256 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. alpha-S1-casein levels (CSN1S1.4695.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha-S1-casein measurement http://www.ebi.ac.uk/efo/EFO_0802272 GCST90240257 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-synuclein levels (SNCA.8458.111.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0009323 GCST90240258 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-synuclein levels (SNCA.8458.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0009323 GCST90240259 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha-taxilin levels (TXLNA.9065.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha-taxilin measurement http://www.ebi.ac.uk/efo/EFO_0801375 GCST90240260 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Alpha/beta hydrolase domain-containing protein 14A levels (ABHD14A.5715.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 alpha/beta hydrolase domain-containing protein 14A measurement http://www.ebi.ac.uk/efo/EFO_0801376 GCST90240261 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ameloblastin levels (AMBN.6522.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ameloblastin measurement http://www.ebi.ac.uk/efo/EFO_0801377 GCST90240262 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amelogenin, X isoform levels (AMELX.8578.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 amelogenin, X isoform measurement http://www.ebi.ac.uk/efo/EFO_0801378 GCST90240263 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. AMP Kinase (alpha1beta1gamma1) levels (PRKAA1.PRKAB1.PRKAG1.5183.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amp kinase (alpha1beta1gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020142 GCST90240264 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. AMP Kinase (alpha2beta2gamma1) levels (PRKAA2.PRKAB2.PRKAG1.5245.40.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amp kinase (alpha2beta2gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020143 GCST90240265 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amphiregulin levels (AREG.2970.60.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amphiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020144 GCST90240266 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B-cell receptor-associated protein 29 levels (BCAP29.11570.94.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 B-cell receptor-associated protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0802301 GCST90240372 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Bactericidal permeability-increasing protein levels (BPI.4126.22.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 bactericidal permeability-increasing protein measurement http://www.ebi.ac.uk/efo/EFO_0020172 GCST90240373 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Baculoviral IAP repeat-containing protein 3 levels (BIRC3.4973.18.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 baculoviral IAP repeat-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020173 GCST90240374 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Baculoviral IAP repeat-containing protein 5 levels (BIRC5.3472.40.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 baculoviral IAP repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020174 GCST90240375 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BAG family molecular chaperone regulator 3 levels (BAG3.10078.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BAG family molecular chaperone regulator 3 measurement http://www.ebi.ac.uk/efo/EFO_0802302 GCST90240376 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. BAG family molecular chaperone regulator 4 levels (BAG4.12844.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 BAG family molecular chaperone regulator 4 measurement http://www.ebi.ac.uk/efo/EFO_0802303 GCST90240377 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Basal Cell Adhesion Molecule levels (BCAM.2816.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 basal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008032 GCST90240378 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Basic leucine zipper transcriptional factor ATF-like 3 levels (BATF3.8858.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 basic leucine zipper transcriptional factor ATF-like 3 measurement http://www.ebi.ac.uk/efo/EFO_0801404 GCST90240379 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Basic salivary proline-rich protein 4 levels (PRB4.12590.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 basic salivary proline-rich protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801405 GCST90240380 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell cycle checkpoint protein RAD1 levels (RAD1.12670.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell cycle checkpoint protein RAD1 measurement http://www.ebi.ac.uk/efo/EFO_0802381 GCST90240655 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell cycle progression protein 1 levels (CCPG1.8889.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell cycle progression protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802382 GCST90240656 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell differentiation protein RCD1 homolog levels (RQCD1.8975.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell differentiation protein RCD1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0802383 GCST90240657 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell division control protein 42 homolog levels (CDC42.9840.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell division control protein 42 homolog measurement http://www.ebi.ac.uk/efo/EFO_0802384 GCST90240658 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell growth regulator with EF hand domain protein 1 levels (CGREF1.6257.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cell growth regulator with EF hand domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801461 GCST90240659 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell surface A33 antigen levels (GPA33.6419.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cell surface A33 antigen measurement http://www.ebi.ac.uk/efo/EFO_0802385 GCST90240660 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell surface glycoprotein CD200 receptor 1 levels (CD200R1.5103.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cell surface glycoprotein CD200 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020253 GCST90240661 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cell surface glycoprotein CD200 receptor 2 levels (CD200R1L.8980.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cell surface glycoprotein CD200 receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0801462 GCST90240662 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cellular retinoic acid-binding protein 1 levels (CRABP1.11967.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 cellular retinoic acid-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801463 GCST90240663 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cellular retinoic acid-binding protein 2 levels (CRABP2.11696.7.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 cellular retinoic acid-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802386 GCST90240664 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Cellular tumor antigen p53 levels (TP53.6152.111.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 cellular tumor antigen p53 measurement http://www.ebi.ac.uk/efo/EFO_0022006 GCST90240665 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Centrin-2 levels (CETN2.13078.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 centrin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801464 GCST90240666 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Centromere protein W levels (CENPW.8864.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 centromere protein W measurement http://www.ebi.ac.uk/efo/EFO_0802387 GCST90240667 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Centrosomal protein of 57 kDa levels (CEP57.11276.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 centrosomal protein of 57 kDa measurement http://www.ebi.ac.uk/efo/EFO_0801465 GCST90240668 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Centrosomal protein of 57 kDa levels (CEP57.9067.152.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 centrosomal protein of 57 kDa measurement http://www.ebi.ac.uk/efo/EFO_0801465 GCST90240669 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Centrosomal protein of 57 kDa levels (CEP57.9905.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 centrosomal protein of 57 kDa measurement http://www.ebi.ac.uk/efo/EFO_0801465 GCST90240670 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiotensin-converting enzyme 2 levels (ACE2.2805.6.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiotensin-converting enzyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0020150 GCST90240292 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ankyrin repeat domain-containing protein 27 levels (ANKRD27.12445.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ankyrin repeat domain-containing protein 27 measurement http://www.ebi.ac.uk/efo/EFO_0802281 GCST90240293 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ankyrin repeat domain-containing protein 46 levels (ANKRD46.7851.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ankyrin repeat domain-containing protein 46 measurement http://www.ebi.ac.uk/efo/EFO_0802282 GCST90240294 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ankyrin-2 levels (ANK2.7624.19.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ankyrin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021874 GCST90240295 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Annexin A1 levels (ANXA1.4960.72.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 annexin A1 measurement http://www.ebi.ac.uk/efo/EFO_0008026 GCST90240296 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATP-dependent DNA helicase Q1 levels (RECQL.11431.235.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATP-dependent DNA helicase Q1 measurement http://www.ebi.ac.uk/efo/EFO_0802293 GCST90240352 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATP-dependent RNA helicase A levels (DHX9.10527.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATP-dependent RNA helicase A measurement http://www.ebi.ac.uk/efo/EFO_0802294 GCST90240353 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATP-dependent RNA helicase DDX25 levels (DDX25.13984.23.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATP-dependent RNA helicase DDX25 measurement http://www.ebi.ac.uk/efo/EFO_0802295 GCST90240354 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATP-dependent RNA helicase DHX8 levels (DHX8.11601.26.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 ATP-dependent RNA helicase DHX8 measurement http://www.ebi.ac.uk/efo/EFO_0801398 GCST90240355 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATPase ASNA1 levels (ASNA1.13620.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATPase ASNA1 measurement http://www.ebi.ac.uk/efo/EFO_0802296 GCST90240356 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATPase family AAA domain-containing protein 1 levels (ATAD1.6625.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATPase family AAA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802297 GCST90240357 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. ATPase family AAA domain-containing protein 2 levels (ATAD2.13043.157.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ATPase family AAA domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802298 GCST90240358 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Atrial natriuretic factor levels (NPPA.5443.62.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 atrial natriuretic factor measurement http://www.ebi.ac.uk/efo/EFO_0004789 GCST90240359 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Augurin levels (C2orf40.6362.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 augurin measurement http://www.ebi.ac.uk/efo/EFO_0801399 GCST90240360 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aurora kinase A levels (AURKA.3091.70.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 aurora kinase A measurement http://www.ebi.ac.uk/efo/EFO_0020168 GCST90240361 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Aurora kinase B levels (AURKB.3346.72.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 aurora kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020169 GCST90240362 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Axin-2 levels (AXIN2.8429.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 6 axin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801400 GCST90240363 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Axin-2 levels (AXIN2.12925.105.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 axin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801400 GCST90240364 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B melanoma antigen 2 levels (BAGE2.6294.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 B melanoma antigen 2 measurement http://www.ebi.ac.uk/efo/EFO_0801401 GCST90240365 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B melanoma antigen 3 levels (BAGE3.6442.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 b melanoma antigen 3 measurement http://www.ebi.ac.uk/efo/EFO_0802299 GCST90240366 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B-cell antigen receptor complex-associated protein alpha chain levels (CD79A.7796.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 B-cell antigen receptor complex-associated protein alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0801402 GCST90240367 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B-cell antigen receptor complex-associated protein beta chain levels (CD79B.6351.55.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 B-cell antigen receptor complex-associated protein beta chain measurement http://www.ebi.ac.uk/efo/EFO_0802300 GCST90240368 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B-cell lymphoma 6 protein levels (BCL6.13640.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 B-cell lymphoma 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0021933 GCST90240369 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B-cell lymphoma/leukemia 10 levels (BCL10.8768.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 B-cell lymphoma/leukemia 10 measurement http://www.ebi.ac.uk/efo/EFO_0801403 GCST90240370 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. B-cell receptor CD22 levels (CD22.2891.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 B-cell receptor CD22 measurement http://www.ebi.ac.uk/efo/EFO_0020171 GCST90240371 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amphoterin-induced protein 1 levels (AMIGO1.9979.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amphoterin-induced protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802273 GCST90240267 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. AMSH-like protease levels (STAMBPL1.12401.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 AMSH-like protease measurement http://www.ebi.ac.uk/efo/EFO_0802274 GCST90240268 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid beta A4 precursor protein-binding family B member 1 levels (APBB1.14206.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amyloid beta A4 precursor protein-binding family B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802275 GCST90240269 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid beta A4 precursor protein-binding family B member 1 levels (APBB1.12822.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amyloid beta A4 precursor protein-binding family B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802275 GCST90240270 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid beta A4 precursor protein-binding family B member 2 levels (APBB2.12753.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 amyloid beta A4 precursor protein-binding family B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801379 GCST90240271 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid beta A4 precursor protein-binding family B member 2 levels (APBB2.12761.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amyloid beta A4 precursor protein-binding family B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801379 GCST90240272 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid beta A4 precursor protein-binding family B member 3 levels (APBB3.13589.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amyloid beta A4 precursor protein-binding family B member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802276 GCST90240273 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid beta A4 protein levels (APP.3171.57.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amyloid beta A4 protein measurement http://www.ebi.ac.uk/efo/EFO_0020145 GCST90240274 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid-like protein 2 levels (APLP2.10627.87.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 amyloid-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801380 GCST90240275 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Amyloid-like protein 2 levels (APLP2.7915.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 amyloid-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801380 GCST90240276 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Anaphase-promoting complex subunit 10 levels (ANAPC10.12345.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 anaphase-promoting complex subunit 10 measurement http://www.ebi.ac.uk/efo/EFO_0802277 GCST90240277 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Anaphase-promoting complex subunit 7 levels (ANAPC7.11690.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 anaphase-promoting complex subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0801381 GCST90240278 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiogenic factor with G patch and FHA domains 1 levels (AGGF1.8051.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiogenic factor with G patch and FHA domains 1 measurement http://www.ebi.ac.uk/efo/EFO_0802278 GCST90240279 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-1 levels (ANGPT1.2811.27.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 angiopoietin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020146 GCST90240280 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-1 receptor, soluble levels (TEK.3773.15.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 angiopoietin-1 receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008023 GCST90240281 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-2 levels (ANGPT2.13660.76.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90240282 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-2 levels (ANGPT2.2602.2.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90240283 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-4 levels (ANGPT4.2500.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020147 GCST90240284 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-like protein 8 levels (C19orf80.7183.102.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-like protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802279 GCST90240285 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-related protein 1 levels (ANGPTL1.9092.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 angiopoietin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801382 GCST90240286 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-related protein 1 levels (ANGPTL1.11142.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801382 GCST90240287 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-related protein 3 levels (ANGPTL3.3281.19.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020148 GCST90240288 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-related protein 4 levels (ANGPTL4.3796.79.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020149 GCST90240289 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiopoietin-related protein 7 levels (ANGPTL7.6371.50.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 angiopoietin-related protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802280 GCST90240290 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Angiostatin levels (PLG.3710.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 angiostatin measurement http://www.ebi.ac.uk/efo/EFO_0008024 GCST90240291 Genome-wide genotyping array 2022-05-13 35472084 Adewuyi EO 2022-01-01 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/35472084 Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways. Endometriosis or asthma (pleiotropy) 17,054 European, Japanese ancestry endometriosis cases, 26,332 European, Japanese ancestry asthma cases, 567,363 European, Japanese ancestry controls NA NR [NR] 67 asthma, endometriosis http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0001065 GCST90102598 Genome-wide genotyping array 2022-05-13 35472084 Adewuyi EO 2022-01-01 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/35472084 Genetic overlap analysis of endometriosis and asthma identifies shared loci implicating sex hormones and thyroid signalling pathways. Endometriosis or asthma (pleiotropy) 17,054 European, Japanese ancestry endometriosis cases, 19,554 European, Japanese ancestry asthma cases, 483,220 European, Japanese ancestry controls NA NR [NR] 60 asthma, endometriosis http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0001065 GCST90102599 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Non-receptor tyrosine-protein kinase TYK2 levels (TYK2.5260.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 non-receptor tyrosine-protein kinase TYK2 measurement http://www.ebi.ac.uk/efo/EFO_0008251 GCST90242128 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Non-secretory ribonuclease levels (RNASE2.8394.56.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 non-secretory ribonuclease measurement http://www.ebi.ac.uk/efo/EFO_0801845 GCST90242129 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Noncompact myelin-associated protein levels (NCMAP.14614.41.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 noncompact myelin-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0802818 GCST90242130 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Normal mucosa of esophagus-specific gene 1 protein levels (NMES1.6406.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 normal mucosa of esophagus-specific gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0801846 GCST90242131 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NT-3 growth factor receptor levels (NTRK3.2658.27.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nt-3 growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020613 GCST90242132 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NTF2-related export protein 1 levels (NXT1.9942.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 NTF2-related export protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801847 GCST90242133 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear envelope phosphatase-regulatory subunit 1 levels (CNEP1R1.13532.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear envelope phosphatase-regulatory subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0802819 GCST90242134 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear factor erythroid 2-related factor 1 levels (NFE2L1.11154.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nuclear factor erythroid 2-related factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801848 GCST90242135 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear migration protein nudC levels (NUDC.8887.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nuclear migration protein nudC measurement http://www.ebi.ac.uk/efo/EFO_0801849 GCST90242136 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear nucleic acid-binding protein C1D levels (C1D.7821.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear nucleic acid-binding protein C1D measurement http://www.ebi.ac.uk/efo/EFO_0802820 GCST90242137 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear pore complex-interacting protein family member B3 levels (NPIPB3.9954.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nuclear pore complex-interacting protein family member B3 measurement http://www.ebi.ac.uk/efo/EFO_0801850 GCST90242138 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear pore membrane glycoprotein 210-like levels (NUP210L.9606.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear pore membrane glycoprotein 210-like measurement http://www.ebi.ac.uk/efo/EFO_0802821 GCST90242139 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear protein localization protein 4 homolog levels (NPLOC4.12993.21.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nuclear protein localization protein 4 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801851 GCST90242140 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear protein MDM1 levels (MDM1.7898.29.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear protein MDM1 measurement http://www.ebi.ac.uk/efo/EFO_0802822 GCST90242141 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear receptor coactivator 2 levels (NCOA2.14045.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nuclear receptor coactivator 2 measurement http://www.ebi.ac.uk/efo/EFO_0801852 GCST90242142 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear receptor ROR-beta levels (RORB.12483.62.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear receptor ROR-beta measurement http://www.ebi.ac.uk/efo/EFO_0802823 GCST90242143 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear receptor subfamily 1 group D member 1 levels (NR1D1.5236.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear receptor subfamily 1 group d member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020614 GCST90242144 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear receptor subfamily 1 group D member 2 levels (NR1D2.12885.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nuclear receptor subfamily 1 group D member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801853 GCST90242145 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear receptor subfamily 4 group A member 1 levels (NR4A1.8089.173.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear receptor subfamily 4 group A member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802824 GCST90242146 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear receptor subfamily 5 group A member 2 levels (NR5A2.12444.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nuclear receptor subfamily 5 group A member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802825 GCST90242147 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear receptor-binding protein levels (NRBP1.12616.45.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 nuclear receptor-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801854 GCST90242148 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nuclear RNA export factor 1 levels (NXF1.12453.161.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nuclear RNA export factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801855 GCST90242149 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nucleolin levels (NCL.13655.34.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nucleolin measurement http://www.ebi.ac.uk/efo/EFO_0801856 GCST90242150 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nucleoside diphosphate kinase A levels (NME1.5909.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nucleoside diphosphate kinase A measurement http://www.ebi.ac.uk/efo/EFO_0009947 GCST90242151 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nucleoside diphosphate kinase B levels (NME2.4249.64.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nucleoside diphosphate kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020615 GCST90242152 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nucleoside diphosphate-linked moiety X motif 8, mitochondrial levels (NUDT8.7872.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nucleoside diphosphate-linked moiety X motif 8, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802826 GCST90242153 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nucleosome assembly protein 1-like 2 levels (NAP1L2.13529.39.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nucleosome assembly protein 1-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801857 GCST90242154 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nutritionally-regulated adipose and cardiac enriched protein homolog levels (NRAC.13464.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nutritionally-regulated adipose and cardiac enriched protein homolog measurement http://www.ebi.ac.uk/efo/EFO_0803300 GCST90242155 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. O-acetyl-ADP-ribose deacetylase MACROD1 levels (MACROD1.13653.335.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 o-acetyl-ADP-ribose deacetylase MACROD1 measurement http://www.ebi.ac.uk/efo/EFO_0802827 GCST90242156 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Obg-like ATPase 1 levels (OLA1.12659.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 obg-like ATPase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801858 GCST90242157 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. OCIA domain-containing protein 1 levels (OCIAD1.3635.76.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 OCIA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008252 GCST90242158 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Odorant-binding protein 2a levels (OBP2A.6526.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 odorant-binding protein 2a measurement http://www.ebi.ac.uk/efo/EFO_0802828 GCST90242159 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Odorant-binding protein 2b levels (OBP2B.5680.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 odorant-binding protein 2b measurement http://www.ebi.ac.uk/efo/EFO_0801859 GCST90242160 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Olfactomedin-like protein 3 levels (OLFML3.8660.33.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 olfactomedin-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802829 GCST90242161 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Olfactomedin-like protein 3 levels (OLFML3.8660.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 olfactomedin-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802829 GCST90242162 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oligophrenin-1 levels (OPHN1.12591.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 oligophrenin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802830 GCST90242163 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oligoribonuclease, mitochondrial levels (REXO2.13590.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 oligoribonuclease, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802831 GCST90242164 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oncostatin-M levels (OSM.2693.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90242165 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oncostatin-M levels (OSM.14063.17.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90242166 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Oncostatin-M-specific receptor subunit beta levels (OSMR.10892.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 oncostatin-M-specific receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801860 GCST90242167 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Opalin levels (OPALIN.7736.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 opalin measurement http://www.ebi.ac.uk/efo/EFO_0801861 GCST90242168 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Opioid-binding protein/cell adhesion molecule levels (OPCML.3634.5.4) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 opioid-binding protein/cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020618 GCST90242169 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Orexigenic neuropeptide QRFP levels (QRFP.6463.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 orexigenic neuropeptide QRFP measurement http://www.ebi.ac.uk/efo/EFO_0802832 GCST90242170 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Origin recognition complex subunit 6 levels (ORC6L.12389.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 origin recognition complex subunit 6 measurement http://www.ebi.ac.uk/efo/EFO_0802833 GCST90242171 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ornithine decarboxylase levels (ODC1.13689.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ornithine decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0802835 GCST90242172 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ornithine decarboxylase antizyme 1 levels (OAZ1.9893.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 ornithine decarboxylase antizyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0802834 GCST90242173 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Orphan sodium- and chloride-dependent neurotransmitter transporter NTT5 levels (SLC6A16.13056.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 orphan sodium- and chloride-dependent neurotransmitter transporter NTT5 measurement http://www.ebi.ac.uk/efo/EFO_0802836 GCST90242174 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Osteocalcin levels (BGLAP.11067.13.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90242175 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Osteoclast-associated immunoglobulin-like receptor levels (OSCAR.7116.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 osteoclast-associated immunoglobulin-like receptor measurement http://www.ebi.ac.uk/efo/EFO_0802837 GCST90242176 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Osteocrin levels (OSTN.7265.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 osteocrin measurement http://www.ebi.ac.uk/efo/EFO_0802838 GCST90242177 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuroligin-1 levels (NLGN1.8052.115.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuroligin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802802 GCST90242078 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuroligin-4, X-linked levels (NLGN4X.5357.60.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuroligin-4, x-linked measurement http://www.ebi.ac.uk/efo/EFO_0020601 GCST90242079 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuromedin-B levels (NMB.9321.400.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuromedin-B measurement http://www.ebi.ac.uk/efo/EFO_0802803 GCST90242080 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuron-specific protein family member 1 levels (NSG1.7802.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuron-specific protein family member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802804 GCST90242081 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuron-specific protein family member 2 levels (NSG2.13409.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 neuron-specific protein family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801832 GCST90242082 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuron-specific vesicular protein calcyon levels (CALY.10671.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuron-specific vesicular protein calcyon measurement http://www.ebi.ac.uk/efo/EFO_0802805 GCST90242083 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuronal cell adhesion molecule levels (NRCAM.5109.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuronal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020602 GCST90242084 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuronal growth regulator 1 levels (NEGR1.13109.82.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuronal growth regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0021932 GCST90242085 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuronal growth regulator 1 levels (NEGR1.7050.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuronal growth regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0021932 GCST90242086 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuronal pentraxin-1 levels (NPTX1.9256.78.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 neuronal pentraxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801833 GCST90242087 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuronal pentraxin-2 levels (NPTX2.6521.35.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neuronal pentraxin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801834 GCST90242088 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuropeptide S levels (NPS.6390.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuropeptide S measurement http://www.ebi.ac.uk/efo/EFO_0802806 GCST90242089 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuropeptide W levels (NPW.9986.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neuropeptide W measurement http://www.ebi.ac.uk/efo/EFO_0801835 GCST90242090 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuropilin and tolloid-like protein 1 levels (NETO1.5639.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuropilin and tolloid-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802807 GCST90242091 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuropilin and tolloid-like protein 2 levels (NETO2.10562.42.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuropilin and tolloid-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802808 GCST90242092 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuropilin-1 levels (NRP1.3214.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neuropilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020603 GCST90242093 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuropilin-2 levels (NRP2.6590.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neuropilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801836 GCST90242094 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurotensin/neuromedin N levels (NTS.7857.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurotensin/neuromedin N measurement http://www.ebi.ac.uk/efo/EFO_0802809 GCST90242095 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurotrophin-3 levels (NTF3.4145.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurotrophin-3 measurement http://www.ebi.ac.uk/efo/EFO_0010791 GCST90242096 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurotrophin-4 levels (NTF4.4146.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurotrophin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020604 GCST90242097 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neutral ceramidase levels (ASAH2.3212.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 4 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90242098 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neutrophil collagenase levels (MMP8.2954.56.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 5 neutrophil collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008248 GCST90242099 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neutrophil cytosol factor 2 levels (NCF2.10047.12.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 neutrophil cytosol factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0801837 GCST90242100 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neutrophil gelatinase-associated lipocalin levels (LCN2.2836.68.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neutrophil gelatinase-associated lipocalin measurement http://www.ebi.ac.uk/efo/EFO_0021964 GCST90242101 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neutrophil-activating peptide 2 levels (PPBP.2790.54.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 neutrophil-activating peptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020606 GCST90242102 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Next to BRCA1 gene 1 protein levels (NBR1.7696.104.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 next to BRCA1 gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0801838 GCST90242103 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Next to BRCA1 gene 1 protein levels (NBR1.7696.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 next to BRCA1 gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0801838 GCST90242104 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NFU1 iron-sulfur cluster scaffold homolog, mitochondrial levels (NFU1.7770.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NFU1 iron-sulfur cluster scaffold homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802810 GCST90242105 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NGFI-A-binding protein 1 levels (NAB1.13933.276.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NGFI-A-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802811 GCST90242106 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NGFI-A-binding protein 2 levels (NAB2.13680.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NGFI-A-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802812 GCST90242107 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NHL repeat-containing protein 3 levels (NHLRC3.9087.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 NHL repeat-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801839 GCST90242108 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NHP2-like protein 1 levels (NHP2L1.13602.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 NHP2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801840 GCST90242109 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nicotinamide phosphoribosyltransferase levels (NAMPT.5011.11.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nicotinamide phosphoribosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0020607 GCST90242110 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nidogen-1 levels (NID1.3213.65.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 nidogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008249 GCST90242111 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nidogen-2 levels (NID2.3633.70.5) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90242112 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Nischarin levels (NISCH.12738.43.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 nischarin measurement http://www.ebi.ac.uk/efo/EFO_0801841 GCST90242113 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2-A/NKG2-B type II integral membrane protein levels (KLRC1.5629.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2-A/NKG2-B type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0802813 GCST90242114 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2-D type II integral membrane protein levels (KLRK1.14095.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2-D type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0008250 GCST90242115 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2-D type II integral membrane protein levels (KLRK1.3056.11.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2-D type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0008250 GCST90242116 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2-E type II integral membrane protein levels (KLRC3.7795.14.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 NKG2-E type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801842 GCST90242117 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2-E type II integral membrane protein levels (KLRC3.11571.75.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2-E type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801842 GCST90242118 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2D ligand 1 levels (ULBP1.14081.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2D ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0802814 GCST90242119 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2D ligand 1 levels (ULBP1.3081.70.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2D ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0802814 GCST90242120 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2D ligand 2 levels (ULBP2.3082.9.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2D ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0802815 GCST90242121 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2D ligand 3 levels (ULBP3.2747.3.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 NKG2D ligand 3 measurement http://www.ebi.ac.uk/efo/EFO_0802816 GCST90242122 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NKG2D ligand 4 levels (RAET1E.7800.85.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 NKG2D ligand 4 measurement http://www.ebi.ac.uk/efo/EFO_0801843 GCST90242123 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. NmrA-like family domain-containing protein 1 levels (NMRAL1.13988.67.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 nmrA-like family domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801844 GCST90242124 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Noggin levels (NOG.5846.24.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 noggin measurement http://www.ebi.ac.uk/efo/EFO_0021995 GCST90242125 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Non-histone chromosomal protein HMG-14 levels (HMGN1.9187.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 non-histone chromosomal protein HMG-14 measurement http://www.ebi.ac.uk/efo/EFO_0021872 GCST90242126 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Non-homologous end-joining factor 1 levels (NHEJ1.11351.233.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 non-homologous end-joining factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802817 GCST90242127 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neural cell adhesion molecule 1 levels (NCAM1.7746.230.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 neural cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0801826 GCST90242053 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neural cell adhesion molecule 1, 120 kDa isoform levels (NCAM1.4498.62.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 neural cell adhesion molecule 1, 120 kda isoform measurement http://www.ebi.ac.uk/efo/EFO_0020593 GCST90242054 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neural cell adhesion molecule 2 levels (NCAM2.6507.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 neural cell adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0801827 GCST90242055 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neural cell adhesion molecule L1 levels (L1CAM.4246.40.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neural cell adhesion molecule L1 measurement http://www.ebi.ac.uk/efo/EFO_0020594 GCST90242056 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neural cell adhesion molecule L1-like protein levels (CHL1.3601.54.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 neural cell adhesion molecule l1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020595 GCST90242057 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neural proliferation differentiation and control protein 1 levels (NPDC1.10424.31.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neural proliferation differentiation and control protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802795 GCST90242058 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuralized-like protein 4 levels (NEURL4.13468.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuralized-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802796 GCST90242059 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuregulin-1 levels (NRG1.9178.30.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuregulin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022029 GCST90242060 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuregulin-4 levels (NRG4.14139.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuregulin-4 measurement http://www.ebi.ac.uk/efo/EFO_0021951 GCST90242061 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurensin-1 levels (NRSN1.11654.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neurensin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801828 GCST90242062 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexin-1 levels (NRXN1.8971.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neurexin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801829 GCST90242063 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexin-1-beta levels (NRXN1.5110.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurexin-1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020596 GCST90242064 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexin-2-beta levels (NRXN2.8876.51.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurexin-2-beta measurement http://www.ebi.ac.uk/efo/EFO_0802797 GCST90242065 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexin-3-beta levels (NRXN3.7093.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 neurexin-3-beta measurement http://www.ebi.ac.uk/efo/EFO_0020597 GCST90242066 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexin-3-beta levels (NRXN3.5111.15.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurexin-3-beta measurement http://www.ebi.ac.uk/efo/EFO_0020597 GCST90242067 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexin-3-beta levels (NRXN3.9799.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurexin-3-beta measurement http://www.ebi.ac.uk/efo/EFO_0020597 GCST90242068 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexophilin-1 levels (NXPH1.4562.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90242069 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurexophilin-3 levels (NXPH3.6054.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurexophilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802798 GCST90242070 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuritin levels (NRN1.8806.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuritin measurement http://www.ebi.ac.uk/efo/EFO_0802799 GCST90242071 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuroblastoma suppressor of tumorigenicity 1 levels (NBL1.2944.66.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuroblastoma suppressor of tumorigenicity 1 measurement http://www.ebi.ac.uk/efo/EFO_0020598 GCST90242072 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuroendocrine convertase 1 levels (PCSK1.13388.57.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 neuroendocrine convertase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801830 GCST90242073 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neuroepithelial cell-transforming gene 1 protein levels (NET1.14260.112.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neuroepithelial cell-transforming gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802800 GCST90242074 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurofascin levels (NFASC.7179.69.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 neurofascin measurement http://www.ebi.ac.uk/efo/EFO_0801831 GCST90242075 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurofilament heavy polypeptide levels (NEFH.9900.36.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 neurofilament heavy polypeptide measurement http://www.ebi.ac.uk/efo/EFO_0802801 GCST90242076 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Neurogenic locus notch homolog protein 1 levels (NOTCH1.5107.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 neurogenic locus notch homolog protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008246 GCST90242077 Genome-wide genotyping array 2022-02-07 34968759 Benjamins JW 2021-12-27 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34968759 Genomic insights in ascending aortic size and distensibility. Ascending aorta maximum area 31,908 individuals NA Affymetrix [NR] 65 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90093369 Genome-wide genotyping array 2022-02-07 34968759 Benjamins JW 2021-12-27 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34968759 Genomic insights in ascending aortic size and distensibility. Ascending aorta minimum area 35,110 individuals NA Affymetrix [NR] 71 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90093370 Genome-wide genotyping array 2022-02-07 34968759 Benjamins JW 2021-12-27 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34968759 Genomic insights in ascending aortic size and distensibility. Ascending aorta distensibility 29,684 individuals NA Affymetrix [NR] 4 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90093371 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 14 levels (SIGLEC14.8248.222.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 9 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90242809 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 14 levels (SIGLEC14.5125.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90242810 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 7 levels (SIGLEC7.2742.68.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90242811 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 8 levels (SIGLEC8.7864.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 sialic acid-binding Ig-like lectin 8 measurement http://www.ebi.ac.uk/efo/EFO_0802067 GCST90242812 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Sialic acid-binding Ig-like lectin 9 levels (SIGLEC9.3007.7.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 sialic acid-binding Ig-like lectin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008286 GCST90242813 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal peptidase complex catalytic subunit SEC11C levels (SEC11C.10658.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 signal peptidase complex catalytic subunit SEC11C measurement http://www.ebi.ac.uk/efo/EFO_0802068 GCST90242814 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal peptide, CUB and EGF-like domain-containing protein 1 levels (SCUBE1.8989.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 signal peptide, CUB and EGF-like domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803074 GCST90242815 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signal transducer and activator of transcription 1-alpha/beta levels (STAT1.12351.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 signal transducer and activator of transcription 1-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0021915 GCST90242816 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signaling lymphocytic activation molecule levels (SLAMF1.7953.20.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 signaling lymphocytic activation molecule measurement http://www.ebi.ac.uk/efo/EFO_0803076 GCST90242824 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Signaling threshold-regulating transmembrane adapter 1 levels (SIT1.11194.6.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 signaling threshold-regulating transmembrane adapter 1 measurement http://www.ebi.ac.uk/efo/EFO_0803077 GCST90242825 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Single Ig IL-1-related receptor levels (SIGIRR.8326.63.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 single Ig IL-1-related receptor measurement http://www.ebi.ac.uk/efo/EFO_0802072 GCST90242826 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Single-pass membrane and coiled-coil domain-containing protein 2 levels (SMCO2.7925.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 single-pass membrane and coiled-coil domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803078 GCST90242827 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Ski-like protein levels (SKIL.14670.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 ski-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802073 GCST90242828 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. SLAM family member 5 levels (CD84.8770.136.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90242829 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GDP-L-fucose synthase levels (TSTA3.12657.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GDP-L-fucose synthase measurement http://www.ebi.ac.uk/efo/EFO_0802564 GCST90241252 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. General transcription factor II-I levels (GTF2I.13609.11.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 general transcription factor II-I measurement http://www.ebi.ac.uk/efo/EFO_0801623 GCST90241253 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GH3 domain-containing protein levels (GHDC.9730.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GH3 domain-containing protein measurement http://www.ebi.ac.uk/efo/EFO_0802565 GCST90241254 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Gigaxonin levels (GAN.10054.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 gigaxonin measurement http://www.ebi.ac.uk/efo/EFO_0802566 GCST90241255 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glia maturation factor gamma levels (GMFG.13062.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glia maturation factor gamma measurement http://www.ebi.ac.uk/efo/EFO_0801624 GCST90241256 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glia-derived nexin levels (SERPINE2.3217.74.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glia-derived nexin measurement http://www.ebi.ac.uk/efo/EFO_0020403 GCST90241257 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glial cell line-derived neurotrophic factor levels (GDNF.5822.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glial cell line-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0021887 GCST90241258 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glial fibrillary acidic protein levels (GFAP.3034.1.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90241259 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glioma pathogenesis-related protein 1 levels (GLIPR1.9265.10.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glioma pathogenesis-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802567 GCST90241260 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucagon levels (GCG.4891.50.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90241261 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucagon-like peptide 1 receptor levels (GLP1R.13085.18.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glucagon-like peptide 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0802568 GCST90241262 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Group XIIB secretory phospholipase A2-like protein levels (PLA2G12B.9380.2.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 group XIIB secretory phospholipase A2-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801657 GCST90241338 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth arrest and DNA damage-inducible proteins-interacting protein 1 levels (GADD45GIP1.9302.90.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 growth arrest and DNA damage-inducible proteins-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803291 GCST90241339 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth arrest-specific protein 1 levels (GAS1.5463.22.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth arrest-specific protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020425 GCST90241340 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth factor receptor-bound protein 14 levels (GRB14.13628.58.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 growth factor receptor-bound protein 14 measurement http://www.ebi.ac.uk/efo/EFO_0801658 GCST90241341 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth factor receptor-bound protein 2 levels (GRB2.5464.52.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 growth factor receptor-bound protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021990 GCST90241342 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth hormone receptor levels (GHR.2948.58.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 growth hormone receptor measurement http://www.ebi.ac.uk/efo/EFO_0020426 GCST90241344 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth-regulated alpha protein levels (CXCL1.2985.35.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST90241345 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 11 levels (GDF11.12060.28.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90241346 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 11 levels (GDF11.14495.161.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90241348 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 11 levels (GDF11.14587.16.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90241349 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 11/8 levels (GDF11.MSTN.2765.4.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 growth/differentiation factor 11/8 measurement http://www.ebi.ac.uk/efo/EFO_0021962 GCST90241350 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 15 levels (GDF15.4374.45.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90241351 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 5 levels (GDF5.2752.62.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 growth/differentiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020429 GCST90241352 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 8 levels (MSTN.12077.32.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth/differentiation factor 8 measurement http://www.ebi.ac.uk/efo/EFO_0021960 GCST90241353 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 8 levels (MSTN.14583.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth/differentiation factor 8 measurement http://www.ebi.ac.uk/efo/EFO_0021960 GCST90241354 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Growth/differentiation factor 9 levels (GDF9.3067.67.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 growth/differentiation factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020430 GCST90241355 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GrpE protein homolog 1, mitochondrial levels (GRPEL1.7113.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 grpE protein homolog 1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802581 GCST90241356 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. GSK3-beta interaction protein levels (GSKIP.12849.25.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 GSK3-beta interaction protein measurement http://www.ebi.ac.uk/efo/EFO_0802582 GCST90241357 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucocorticoid modulatory element-binding protein 2 levels (GMEB2.12804.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glucocorticoid modulatory element-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802569 GCST90241263 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucocorticoid receptor levels (NR3C1.2857.70.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glucocorticoid receptor measurement http://www.ebi.ac.uk/efo/EFO_0020405 GCST90241264 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucokinase levels (GCK.12960.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glucokinase measurement http://www.ebi.ac.uk/efo/EFO_0801625 GCST90241265 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucokinase regulatory protein levels (GCKR.5223.59.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glucokinase regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0020406 GCST90241266 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucosamine 6-phosphate N-acetyltransferase levels (GNPNAT1.13954.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glucosamine 6-phosphate N-acetyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0801626 GCST90241267 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucosamine-6-phosphate isomerase 1 levels (GNPDA1.8909.77.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glucosamine-6-phosphate isomerase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801627 GCST90241268 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucose-6-phosphate isomerase levels (GPI.4272.46.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glucose-6-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020407 GCST90241269 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucosidase 2 subunit beta levels (PRKCSH.5687.5.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glucosidase 2 subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801628 GCST90241270 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glucoside xylosyltransferase 1 levels (GXYLT1.8229.1.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 glucoside xylosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801629 GCST90241271 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutamate carboxypeptidase 2 levels (FOLH1.3218.8.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90241272 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutamate carboxypeptidase 2 levels (FOLH1.5478.50.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90241273 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutamate receptor 4 levels (GRIA4.10760.107.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 3 glutamate receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0801630 GCST90241274 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutamate receptor ionotropic, delta-2 levels (GRID2.12758.47.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glutamate receptor ionotropic, delta-2 measurement http://www.ebi.ac.uk/efo/EFO_0801631 GCST90241275 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutaminyl-peptide cyclotransferase levels (QPCT.7849.3.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glutaminyl-peptide cyclotransferase measurement http://www.ebi.ac.uk/efo/EFO_0802570 GCST90241276 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutaminyl-peptide cyclotransferase-like protein levels (QPCTL.8866.53.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glutaminyl-peptide cyclotransferase-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801632 GCST90241277 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutaredoxin-2, mitochondrial levels (GLRX2.12486.8.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glutaredoxin-2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801633 GCST90241278 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutaredoxin-like protein C5orf63 levels (C5orf63.13378.80.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glutaredoxin-like protein C5orf63 measurement http://www.ebi.ac.uk/efo/EFO_0801634 GCST90241279 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione peroxidase 7 levels (GPX7.8345.27.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glutathione peroxidase 7 measurement http://www.ebi.ac.uk/efo/EFO_0801635 GCST90241280 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase A1 levels (GSTA1.12446.49.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glutathione S-transferase A1 measurement http://www.ebi.ac.uk/efo/EFO_0801636 GCST90241281 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase A3 levels (GSTA3.4993.16.1) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glutathione s-transferase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020409 GCST90241282 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase A4 levels (GSTA4.14645.253.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glutathione S-transferase A4 measurement http://www.ebi.ac.uk/efo/EFO_0801637 GCST90241283 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase kappa 1 levels (GSTK1.13474.40.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 0 glutathione S-transferase kappa 1 measurement http://www.ebi.ac.uk/efo/EFO_0802571 GCST90241284 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase Mu 1 levels (GSTM1.7239.9.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 1 glutathione S-transferase Mu 1 measurement http://www.ebi.ac.uk/efo/EFO_0801638 GCST90241285 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase omega-1 levels (GSTO1.12436.84.3) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glutathione S-transferase omega-1 measurement http://www.ebi.ac.uk/efo/EFO_0801639 GCST90241286 Genome-wide genotyping array 2023-01-10 29875488 Sun BB 2018-06-06 Nature www.ncbi.nlm.nih.gov/pubmed/29875488 Genomic atlas of the human plasma proteome. Glutathione S-transferase P levels (GSTP1.4911.49.2) 3,301 European ancestry individuals NA Affymetrix [10572788] (imputed) 2 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90241287 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131122 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130856 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130857 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130858 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130859 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130860 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130861 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130862 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130863 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130864 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130865 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130866 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130867 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130932 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130933 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130934 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130935 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130936 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130937 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130938 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130939 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130940 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130941 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130942 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130943 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130994 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130995 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130996 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130997 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130998 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130999 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131000 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131001 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131002 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131003 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131004 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131005 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131006 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131007 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131008 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131009 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131010 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131011 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131012 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131013 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131014 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131015 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131016 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131017 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131018 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130969 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130970 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130971 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130972 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130973 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130974 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130975 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130976 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130977 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130978 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130979 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130980 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130981 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130868 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130869 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130870 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130871 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130872 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130873 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130874 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130875 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130876 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130877 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130878 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130879 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130944 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130945 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130946 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130947 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130948 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130949 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130950 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130951 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130952 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130953 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130954 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130955 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130956 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130957 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130958 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130959 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130960 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130961 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130962 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130963 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130964 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130965 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130966 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130967 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130968 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130880 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130881 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130882 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130883 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130884 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130885 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130886 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130887 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130888 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130889 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130890 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130891 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130892 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130893 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130894 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130895 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130896 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130897 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130898 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130899 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130900 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130901 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130902 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130903 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130904 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130905 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130906 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130907 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130908 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130909 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130910 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130911 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130912 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130913 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130914 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130915 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130916 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130917 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130982 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130983 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130984 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130985 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130986 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130987 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130988 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130989 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130990 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130991 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130992 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130993 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129659 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129660 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129661 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129662 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129663 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129664 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129665 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129666 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129667 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129668 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129669 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129670 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129671 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129672 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129673 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129674 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129675 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129676 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129677 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129678 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129679 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129680 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129681 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129682 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129683 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131044 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131045 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131046 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131047 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131048 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131049 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131050 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131051 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131052 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131053 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131054 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131055 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131056 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131057 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131058 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131059 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131060 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131061 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131062 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131063 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130918 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130919 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130920 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130921 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131064 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131065 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131066 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131067 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131068 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131069 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131070 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131071 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131072 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131073 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131074 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131075 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131076 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131077 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131078 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131079 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_2) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129649 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_3) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129650 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_3) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129651 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129652 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129653 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129654 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129655 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129656 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129657 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129658 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131019 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131020 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131021 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131022 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131023 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131024 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131025 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131026 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131027 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131028 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131029 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131030 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131031 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131032 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131033 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair48_49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131034 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131035 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131036 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131037 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131038 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131039 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131040 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131041 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131042 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131043 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair15_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129768 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129769 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129770 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129771 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129772 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129773 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129774 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129775 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129776 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129777 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129778 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129779 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129780 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129781 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129714 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129715 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129716 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129717 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129718 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129719 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129720 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129721 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129722 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129723 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129724 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129684 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129685 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129686 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129687 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129688 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129689 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129690 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129691 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129692 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129693 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129694 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129695 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129696 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129697 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129698 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129699 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129700 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129701 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129702 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129703 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129704 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129705 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129706 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129707 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129708 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129709 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129710 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129711 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129712 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair14_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129782 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129713 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129749 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129750 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129751 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129752 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair14_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129753 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129754 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129755 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129756 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129757 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129758 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129759 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129760 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129761 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129762 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129763 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129764 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129765 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129766 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair14_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129767 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129725 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129726 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129727 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129728 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129729 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129730 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129731 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129732 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129733 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129734 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129735 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129736 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129737 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129738 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129739 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129740 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129741 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129742 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129743 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129744 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129745 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129746 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129747 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129748 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131168 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131194 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131195 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131196 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131197 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131198 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131199 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131200 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131201 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131202 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131203 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131204 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131205 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131206 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131207 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131208 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131209 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131210 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131211 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131212 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131213 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131214 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131215 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131216 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131217 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131218 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131169 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131170 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131171 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131172 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131173 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131174 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131175 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131176 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131177 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131178 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131179 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131180 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair48_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131181 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair49_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131182 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair50_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131183 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair51_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131184 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131185 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131186 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131187 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131188 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131189 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131190 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131191 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131192 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131193 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131219 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131220 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131221 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131222 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131223 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131224 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131225 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131226 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131227 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131228 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131229 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131230 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131231 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair48_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131232 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair49_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131233 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair50_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131234 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair51_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131235 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair52_53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131236 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131237 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131238 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131239 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131240 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131241 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131242 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131243 Genome-wide genotyping array 2022-09-12 35851147 Adewuyi EO 2022-07-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35851147 A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer's disease and gastrointestinal tract disorders. Alzheimer's disease or gastroesophageal reflux disease 71,880 European ancestry Alzheimer's disease or AD-by-proxy cases, 71,522 European ancestry GERD cases, up to 644,457 European ancestry controls NA NR [NR] 186 Alzheimer disease, gastroesophageal reflux disease http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90134603 Genome-wide genotyping array 2022-09-12 35851147 Adewuyi EO 2022-07-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35851147 A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer's disease and gastrointestinal tract disorders. Alzheimer's disease or peptic ulcer disease 71,880 European ancestry Alzheimer's disease or AD-by-proxy cases, 16,666 European ancestry peptic ulcer disease cases, up to 823,039 European ancestry controls NA NR [NR] 31 Alzheimer disease, peptic ulcer disease http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/MONDO_0004247 GCST90134604 Genome-wide genotyping array 2022-09-12 35851147 Adewuyi EO 2022-07-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35851147 A large-scale genome-wide cross-trait analysis reveals shared genetic architecture between Alzheimer's disease and gastrointestinal tract disorders. Alzheimer's disease or gastroesophageal reflux disease and/or peptic ulcer disease 71,880 European ancestry Alzheimer's disease or AD-by-proxy cases, 90,175 European ancestry peptic ulcer disease and/or GERD and/or medications for their treatment cases, up to 749,530 European ancestry controls NA NR [NR] 14 Alzheimer disease, peptic ulcer disease, Peptic ulcer and gastro-oesophageal reflux disease (GORD) drug use measurement, gastroesophageal reflux disease http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/MONDO_0004247, http://www.ebi.ac.uk/efo/EFO_0009923, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90134605 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net_Edge_ICA1) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131344 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net_Edge_ICA2) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 5 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131345 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net_Edge_ICA3) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131346 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net_Edge_ICA4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131347 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net_Edge_ICA5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131348 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net_Edge_ICA6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131349 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node1) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131350 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node2) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131351 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node3) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131352 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131353 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131354 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131355 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131356 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131357 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131358 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131359 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131360 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131361 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131362 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131363 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131364 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131365 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131366 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131367 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131368 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131244 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131245 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131246 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131247 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131248 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131249 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131250 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131251 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131252 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131253 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131254 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131255 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131256 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131257 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131258 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131259 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131260 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131261 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131262 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131263 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131264 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131265 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131266 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131267 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131268 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131294 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131295 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131296 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131297 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131298 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131299 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131300 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131301 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131302 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131303 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131304 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131305 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131306 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131307 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131308 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131309 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131310 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131311 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131312 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131313 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131314 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131315 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131316 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131317 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131318 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131269 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131270 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131271 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131272 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131273 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131274 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131275 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131276 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131277 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131278 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131279 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131280 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131281 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131282 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131283 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair48_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131284 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair49_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131285 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair50_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131286 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair51_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131287 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair52_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131288 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair53_54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131289 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131290 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131291 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131292 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131293 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131319 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131320 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131321 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131322 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131323 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131324 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131325 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131326 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131327 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131328 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131329 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131330 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131331 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131332 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131333 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131334 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131335 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131336 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair48_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131337 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair49_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131338 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair50_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131339 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair51_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131340 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair52_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131341 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair53_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131342 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair54_55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131343 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131394 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131395 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131396 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131397 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131398 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131399 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131400 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131401 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131402 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131403 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131404 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131405 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131406 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131407 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131408 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131409 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131410 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131411 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131412 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131413 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131414 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131415 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131416 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131417 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node48) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131418 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131369 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net25_Node21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 4 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131370 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node1) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131371 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node2) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131372 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node3) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131373 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131374 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131375 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131376 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131377 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131378 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131379 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131380 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131381 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131382 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131383 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131384 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131385 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131386 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 3 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131387 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131388 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131389 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131390 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131391 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131392 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131393 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node49) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 2 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131419 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131420 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131421 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131422 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node53) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131423 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node54) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131424 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (amplitude of low frequency fluctations) (Net100_Node55) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131425 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131123 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131124 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131125 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131126 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131127 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair45_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131128 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131129 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131130 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair48_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131131 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair49_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131132 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair50_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131133 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131134 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131135 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131136 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131137 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131138 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131139 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131140 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131141 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131142 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131143 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131144 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131145 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131146 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131147 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131148 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131149 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131150 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131151 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131152 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131153 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131154 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131155 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131156 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131157 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131158 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131159 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131160 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131161 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131162 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131163 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131164 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131165 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131166 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_52) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131167 Genome-wide genotyping array 2022-09-13 35771237 Liu Q 2022-06-30 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35771237 A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome. Type 2 diabetes or polycystic ovary syndrome (pleiotropy) upto 74,124 type 2 diabetes European ancestry cases, upto 824,006 European ancestry controls without type 2 diabetes, upto 10,074 polycystic ovary syndrome European ancestry cases, upto 103,164 polycystic ovary syndrome European ancestry controls without polycystic ovary syndrome NA NR [NR] 4 polycystic ovary syndrome, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000660, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90134404 Genome-wide genotyping array 2022-09-13 35771237 Liu Q 2022-06-30 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35771237 A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome. Type 2 diabetes (adjusted for BMI) or polycystic ovary syndrome (pleiotropy) upto 74,124 type 2 diabetes European ancestry cases, upto 824,006 European ancestry controls without type 2 diabetes, upto 10,074 polycystic ovary syndrome European ancestry cases, upto 103,164 polycystic ovary syndrome European ancestry controls without polycystic ovary syndrome NA NR [NR] 5 polycystic ovary syndrome, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000660, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90134405 Genome-wide genotyping array 2022-09-13 35771237 Liu Q 2022-06-30 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35771237 A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome. Fasting glucose (adjusted for BMI) or polycystic ovary syndrome (pleiotropy) upto 20,000 European ancestry individuals with fasting glucose, upto 10,074 polycystic ovary syndrome European ancestry cases, upto 103,164 polycystic ovary syndrome European ancestry controls without polycystic ovary syndrome NA NR [NR] 3 polycystic ovary syndrome, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0000660, http://www.ebi.ac.uk/efo/EFO_0004465 GCST90134406 Genome-wide genotyping array 2022-09-13 35771237 Liu Q 2022-06-30 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35771237 A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome. Fasting insulin (adjusted for BMI) or polycystic ovary syndrome (pleiotropy) upto 20,000 European ancestry individuals with fasting insulin, upto 10,074 polycystic ovary syndrome European ancestry cases, upto 103,164 polycystic ovary syndrome European ancestry controls without polycystic ovary syndrome NA NR [NR] 3 polycystic ovary syndrome, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0000660, http://www.ebi.ac.uk/efo/EFO_0004466 GCST90134407 Genome-wide genotyping array 2022-09-13 35771237 Liu Q 2022-06-30 Diabetologia www.ncbi.nlm.nih.gov/pubmed/35771237 A genome-wide cross-trait analysis identifies shared loci and causal relationships of type 2 diabetes and glycaemic traits with polycystic ovary syndrome. HbA1c or polycystic ovary syndrome (pleiotropy) upto 20,000 European ancestry individuals with HbA1c, upto 10,074 polycystic ovary syndrome European ancestry cases, upto 103,164 polycystic ovary syndrome European ancestry controls without polycystic ovary syndrome NA NR [NR] 4 HbA1c measurement, polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0004541, http://www.ebi.ac.uk/efo/EFO_0000660 GCST90134408 Genome-wide genotyping array 2022-09-05 35768473 Reay WR 2022-06-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35768473 The genetic architecture of pneumonia susceptibility implicates mucin biology and a relationship with psychiatric illness. Pneumonia 74,323 European ancestry cases, 316,721 European ancestry controls NA NR [NR] (imputed) 5 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90134363 Genome-wide genotyping array 2022-03-23 34864618 Bourgeois S 2021-12-02 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34864618 Genome-Wide association between EYA1 and Aspirin-induced peptic ulceration. NSAID-induced peptic ulcer disease 235 European ancestry cases, 441 European ancestry controls 206 European ancestry cases, 309 European ancestry controls Illumina [5548084] (imputed) 1 peptic ulcer disease, response to non-steroidal anti-inflammatory http://purl.obolibrary.org/obo/MONDO_0004247, http://www.ebi.ac.uk/efo/EFO_0005533 GCST90096798 Genome-wide genotyping array 2021-09-09 34098431 Ning K 2021-04-20 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/34098431 Improving brain age estimates with deep learning leads to identification of novel genetic factors associated with brain aging. Relative brain age 16,998 European ancestry individuals NA NR [538476] 3 brain age measurement http://www.ebi.ac.uk/efo/EFO_0010602 GCST012361 Genome-wide genotyping array 2022-03-30 34834585 Zazuli Z 2021-11-20 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834585 Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation Study. Cisplatin-induced nephrotoxicity (increased serum creatinine AKI-CTCAE) 608 European ancestry individuals NA Illumina [6500000] (imputed) 3 response to cisplatin http://purl.obolibrary.org/obo/GO_0072718 GCST90096814 Genome-wide genotyping array 2022-03-30 34834585 Zazuli Z 2021-11-20 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834585 Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation Study. Cisplatin-induced nephrotoxicity (decreased eGFR) 608 European ancestry individuals NA Illumina [6500000] (imputed) 4 response to cisplatin http://purl.obolibrary.org/obo/GO_0072718 GCST90096815 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worrier / anxious feelings (UKB data field 1980) 251,982 European ancestry cases, 192,422 European ancestry controls NA NR [11842647] (imputed) 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90041879 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignant neoplasm (PheCode 198) 274 European ancestry cases, 456,074 European ancestry controls NA NR [11842647] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90041880 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tense / highly strung (UKB data field 1990) 76,946 European ancestry cases, 364,942 European ancestry controls NA NR [11842647] (imputed) 0 feeling tense measurement http://www.ebi.ac.uk/efo/EFO_0009596 GCST90041881 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neoplasm of uncertain behavior (PheCode 199) 1,006 European ancestry cases, 455,342 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system neoplasm http://www.ebi.ac.uk/efo/EFO_0003853 GCST90041882 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Polycythemia vera (PheCode 200.1) 334 European ancestry cases, 456,014 European ancestry controls NA NR [11842647] (imputed) 0 polycythemia vera http://www.ebi.ac.uk/efo/EFO_0002429 GCST90041883 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Worry too long after embarrassment (UKB data field 2000) 208,944 European ancestry cases, 228,751 European ancestry controls NA NR [11842647] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90041884 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: lung cancer (UKB data field 20001_1001) 267 European ancestry cases, 456,009 European ancestry controls NA NR [11842647] (imputed) 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90041885 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: breast cancer (UKB data field 20001_1002) 10,152 European ancestry cases, 446,124 European ancestry controls NA NR [11842647] (imputed) 2 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90041886 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Intestinal infection due to C. difficile (PheCode 8.52) 223 European ancestry cases, 456,125 European ancestry controls NA NR [11842647] (imputed) 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90041704 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bacterial enteritis (PheCode 8.5) 1,066 European ancestry cases, 455,282 European ancestry controls NA NR [11842647] (imputed) 0 enteritis http://purl.obolibrary.org/obo/MONDO_0043579 GCST90041705 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Viral Enteritis (PheCode 8.6) 755 European ancestry cases, 455,593 European ancestry controls NA NR [11842647] (imputed) 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90041706 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Intestinal infection (PheCode 8) 3,521 European ancestry cases, 452,827 European ancestry controls NA NR [11842647] (imputed) 0 intestinal infectious disease http://purl.obolibrary.org/obo/MONDO_0000916 GCST90041707 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tuberculosis (PheCode 10) 99 European ancestry cases, 456,249 European ancestry controls NA NR [11842647] (imputed) 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90041708 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gram negative septicemia (PheCode 38.1) 383 European ancestry cases, 455,965 European ancestry controls NA NR [11842647] (imputed) 0 bacteriemia http://www.ebi.ac.uk/efo/EFO_0003033 GCST90041709 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Gram positive septicemia (PheCode 38.2) 168 European ancestry cases, 456,180 European ancestry controls NA NR [11842647] (imputed) 0 bacteriemia http://www.ebi.ac.uk/efo/EFO_0003033 GCST90041710 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Septicemia (PheCode 38) 1,634 European ancestry cases, 454,714 European ancestry controls NA NR [11842647] (imputed) 0 bacteriemia http://www.ebi.ac.uk/efo/EFO_0003033 GCST90041711 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bacterial infection, not otherwise specified (PheCode 41) 139 European ancestry cases, 456,209 European ancestry controls NA NR [11842647] (imputed) 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90041712 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Herpes zoster (PheCode 53) 170 European ancestry cases, 456,178 European ancestry controls NA NR [11842647] (imputed) 0 susceptibility to shingles measurement http://www.ebi.ac.uk/efo/EFO_0008401 GCST90041713 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Viral hepatitis C (PheCode 70.3) 219 European ancestry cases, 456,129 European ancestry controls NA NR [11842647] (imputed) 0 hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0003047 GCST90041714 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Chronic hepatitis (PheCode 70.4) 181 European ancestry cases, 456,167 European ancestry controls NA NR [11842647] (imputed) 0 chronic hepatitis http://www.ebi.ac.uk/efo/EFO_0008496 GCST90041715 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Hepatitis, not otherwise specified (PheCode 70.9) 236 European ancestry cases, 456,112 European ancestry controls NA NR [11842647] (imputed) 0 Hepatitis http://purl.obolibrary.org/obo/HP_0012115 GCST90041716 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. HIV infection, symptomatic (PheCode 71.1) 78 European ancestry cases, 208,730 European ancestry controls NA NR [11842647] (imputed) 0 AIDS http://www.ebi.ac.uk/efo/EFO_0000765 GCST90041717 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Viral warts & HPV (PheCode 78) 756 European ancestry cases, 455,592 European ancestry controls NA NR [11842647] (imputed) 0 common wart http://www.ebi.ac.uk/efo/EFO_0009662 GCST90041718 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Viral infection (PheCode 79) 1,621 European ancestry cases, 454,727 European ancestry controls NA NR [11842647] (imputed) 0 Chlamydiaceae Infections http://www.ebi.ac.uk/efo/EFO_1001288 GCST90041719 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Postoperative infection (PheCode 80) 3,056 European ancestry cases, 453,292 European ancestry controls NA NR [11842647] (imputed) 0 post-operative sign or symptom http://www.ebi.ac.uk/efo/EFO_0005323 GCST90041720 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of testis (PheCode 187.2) 284 European ancestry cases, 208,524 European ancestry controls NA NR [11842647] (imputed) 0 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST90041854 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of other male genital organs (PheCode 187) 41 European ancestry cases, 208,767 European ancestry controls NA NR [11842647] (imputed) 0 male reproductive organ cancer http://www.ebi.ac.uk/efo/EFO_0007355 GCST90041855 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of kidney, except pelvis (PheCode 189.11) 988 European ancestry cases, 455,360 European ancestry controls NA NR [11842647] (imputed) 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90041856 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of bladder (PheCode 189.21) 2,264 European ancestry cases, 454,084 European ancestry controls NA NR [11842647] (imputed) 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90041857 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of bladder (PheCode 189.2) 762 European ancestry cases, 455,586 European ancestry controls NA NR [11842647] (imputed) 0 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90041858 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of other urinary organs (PheCode 189.4) 105 European ancestry cases, 456,243 European ancestry controls NA NR [11842647] (imputed) 0 Malignant Urinary System Neoplasm http://www.ebi.ac.uk/efo/EFO_1000363 GCST90041859 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of eye (PheCode 190) 183 European ancestry cases, 456,165 European ancestry controls NA NR [11842647] (imputed) 0 eye neoplasm http://www.ebi.ac.uk/efo/EFO_0003824 GCST90041860 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of brain (PheCode 191.11) 497 European ancestry cases, 455,851 European ancestry controls NA NR [11842647] (imputed) 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90041861 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant and unknown neoplasms of brain and nervous system (PheCode 191) 175 European ancestry cases, 456,173 European ancestry controls NA NR [11842647] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90041862 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Mood swings (UKB data field 1920) 201,373 European ancestry cases, 243,901 European ancestry controls NA NR [11842647] (imputed) 0 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST90041863 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Miserableness (UKB data field 1930) 192,681 European ancestry cases, 255,873 European ancestry controls NA NR [11842647] (imputed) 0 feeling miserable measurement http://www.ebi.ac.uk/efo/EFO_0009598 GCST90041864 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Thyroid cancer (PheCode 193) 379 European ancestry cases, 455,969 European ancestry controls NA NR [11842647] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90041865 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Irritability (UKB data field 1940) 122,939 European ancestry cases, 313,092 European ancestry controls NA NR [11842647] (imputed) 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90041866 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm, other (PheCode 195.1) 940 European ancestry cases, 455,408 European ancestry controls NA NR [11842647] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90041867 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sensitivity hurt feelings (UKB data field 1950) 246,088 European ancestry cases, 196,977 European ancestry controls NA NR [11842647] (imputed) 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90041868 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer, suspected or other (PheCode 195) 713 European ancestry cases, 455,635 European ancestry controls NA NR [11842647] (imputed) 0 carcinoma http://www.ebi.ac.uk/efo/EFO_0000313 GCST90041869 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fed up feelings (UKB data field 1960) 181,740 European ancestry cases, 265,002 European ancestry controls NA NR [11842647] (imputed) 0 feeling "fed-up" measurement http://www.ebi.ac.uk/efo/EFO_0009588 GCST90041870 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Nervous feelings (UKB data field 1970) 105,190 European ancestry cases, 339,154 European ancestry controls NA NR [11842647] (imputed) 0 feeling nervous measurement http://www.ebi.ac.uk/efo/EFO_0009597 GCST90041871 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignancy of lymph nodes (PheCode 198.1) 908 European ancestry cases, 455,440 European ancestry controls NA NR [11842647] (imputed) 0 lymph node neoplasm http://purl.obolibrary.org/obo/MONDO_0024339 GCST90041872 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignancy of respiratory organs (PheCode 198.2) 801 European ancestry cases, 455,547 European ancestry controls NA NR [11842647] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90041873 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignant neoplasm of digestive systems (PheCode 198.3) 582 European ancestry cases, 455,766 European ancestry controls NA NR [11842647] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90041874 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignant neoplasm of liver (PheCode 198.4) 835 European ancestry cases, 455,513 European ancestry controls NA NR [11842647] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90041875 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignancy of brain/spine (PheCode 198.5) 464 European ancestry cases, 455,884 European ancestry controls NA NR [11842647] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90041876 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignancy of bone (PheCode 198.6) 927 European ancestry cases, 455,421 European ancestry controls NA NR [11842647] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90041877 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Secondary malignant neoplasm of skin (PheCode 198.7) 107 European ancestry cases, 456,241 European ancestry controls NA NR [11842647] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90041878 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: cholesterol lowering milk (UKB data field 100920_2110) 125 European ancestry cases, 63,876 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041746 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: other type of milk (UKB data field 100920_2199) 304 European ancestry cases, 63,697 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041747 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: don't know type of milk (UKB data field 100920_222) 122 European ancestry cases, 63,879 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041748 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bread consumed (UKB data field 100940) 54,755 European ancestry cases, 9,246 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041749 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Injury, not otherwise specified (PheCode 1009) 6,242 European ancestry cases, 450,106 European ancestry controls NA NR [11842647] (imputed) 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90041750 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other tests (PheCode 1010) 4,249 European ancestry cases, 452,099 European ancestry controls NA NR [11842647] (imputed) 0 animal viral hepatitis http://www.ebi.ac.uk/efo/EFO_0007540 GCST90041751 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Complications of surgical and medical procedures (PheCode 1011) 1,836 European ancestry cases, 454,512 European ancestry controls NA NR [11842647] (imputed) 0 complication http://www.ebi.ac.uk/efo/EFO_0009518 GCST90041752 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Effects of other external causes (PheCode 1015) 1,093 European ancestry cases, 455,255 European ancestry controls NA NR [11842647] (imputed) 0 response to stress http://purl.obolibrary.org/obo/GO_0006950 GCST90041753 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other ill-defined and unknown causes of morbidity and mortality (PheCode 1019) 10,656 European ancestry cases, 445,692 European ancestry controls NA NR [11842647] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90041754 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Yogurt/ice-cream consumers (UKB data field 102080) 25,938 European ancestry cases, 38,063 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041755 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Dessert consumers (UKB data field 102130) 20,622 European ancestry cases, 43,379 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041756 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Sweet snack consumers (UKB data field 102250) 34,656 European ancestry cases, 29,345 European ancestry controls NA NR [11842647] (imputed) 0 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST90041757 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Savoury snack consumers (UKB data field 102400) 22,768 European ancestry cases, 41,233 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041758 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Starchy food consumers (UKB data field 102700) 17,215 European ancestry cases, 46,786 European ancestry controls NA NR [11842647] (imputed) 0 carbohydrate intake measurement http://www.ebi.ac.uk/efo/EFO_0010811 GCST90041759 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cheese consumers (UKB data field 102800) 28,953 European ancestry cases, 35,048 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041760 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Egg consumers (UKB data field 102930) 13,484 European ancestry cases, 50,517 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041761 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Meat consumers (UKB data field 103000) 44,190 European ancestry cases, 19,811 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041762 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fat removed from meat (UKB data field 103120) 1,241 European ancestry cases, 15,450 European ancestry controls NA NR [11842647] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90041763 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Skin removed from poultry (UKB data field 103130) 247 European ancestry cases, 13,768 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041764 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fish consumer (UKB data field 103140) 18,431 European ancestry cases, 45,570 European ancestry controls NA NR [11842647] (imputed) 0 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST90041765 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vegetarian alternatives intake (UKB data field 103250) 2,260 European ancestry cases, 61,741 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041766 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vegetable consumers (UKB data field 103990) 52,696 European ancestry cases, 11,305 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041767 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Fruit consumers (UKB data field 104400) 52,183 European ancestry cases, 11,818 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041768 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: skin cancer (UKB data field 20001_1003) 1,428 European ancestry cases, 454,848 European ancestry controls NA NR [11842647] (imputed) 0 skin carcinoma http://www.ebi.ac.uk/efo/EFO_0009259 GCST90041887 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: cancer of lip/mouth/pharynx/oral cavity (UKB data field 20001_1004) 101 European ancestry cases, 456,175 European ancestry controls NA NR [11842647] (imputed) 0 oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0005570 GCST90041888 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: larynx/throat cancer (UKB data field 20001_1006) 341 European ancestry cases, 455,935 European ancestry controls NA NR [11842647] (imputed) 0 laryngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0003817 GCST90041889 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: tongue cancer (UKB data field 20001_1011) 144 European ancestry cases, 456,132 European ancestry controls NA NR [11842647] (imputed) 0 tongue neoplasm http://www.ebi.ac.uk/efo/EFO_0003871 GCST90041890 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - senna (UKB data field 20003_1140865716) 852 European ancestry cases, 455,424 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042019 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ispaghula husk (UKB data field 20003_1140865752) 417 European ancestry cases, 455,859 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042020 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bisacodyl (UKB data field 20003_1140865786) 173 European ancestry cases, 456,103 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042021 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lactulose product (UKB data field 20003_1140865800) 1,185 European ancestry cases, 455,091 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042022 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - anusol cream (UKB data field 20003_1140865816) 114 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042023 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - magnesium citrate (UKB data field 20003_1140865872) 163 European ancestry cases, 456,113 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042024 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - creon e/c granules in capsule (UKB data field 20003_1140866026) 242 European ancestry cases, 456,034 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042025 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - indapamide (UKB data field 20003_1140866078) 1,424 European ancestry cases, 454,852 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042026 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - frusemide (UKB data field 20003_1140866116) 787 European ancestry cases, 455,489 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042027 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bendrofluazide (UKB data field 20003_1140866122) 2,431 European ancestry cases, 453,845 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042028 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - spironolactone (UKB data field 20003_1140866236) 841 European ancestry cases, 455,435 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042029 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - bumetanide (UKB data field 20003_1140866280) 364 European ancestry cases, 455,912 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042030 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - securon 40mg tablet (UKB data field 20003_1140866466) 114 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042031 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - atenolol (UKB data field 20003_1140866738) 17,684 European ancestry cases, 438,592 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042032 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - half-inderal la 80mg m/r capsule (UKB data field 20003_1140866800) 169 European ancestry cases, 456,107 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042033 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - inderal 10mg tablet (UKB data field 20003_1140866804) 114 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042034 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - risperidone (UKB data field 20003_1140867444) 219 European ancestry cases, 456,057 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042035 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lithium product (UKB data field 20003_1140867490) 443 European ancestry cases, 455,833 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042036 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - priadel 200mg m/r tablet (UKB data field 20003_1140867504) 286 European ancestry cases, 455,990 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042037 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lofepramine (UKB data field 20003_1140867726) 352 European ancestry cases, 455,924 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042038 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nortriptyline (UKB data field 20003_1140867818) 264 European ancestry cases, 456,012 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042039 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - prozac 20mg capsule (UKB data field 20003_1140867876) 619 European ancestry cases, 455,657 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042040 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - sertraline (UKB data field 20003_1140867878) 1,911 European ancestry cases, 454,365 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042041 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Infection/inflammation of internal prosthetic device; implant; and graft (PheCode 81) 1,019 European ancestry cases, 455,329 European ancestry controls NA NR [11842647] (imputed) 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90041721 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Burns (PheCode 1000) 487 European ancestry cases, 455,861 European ancestry controls NA NR [11842647] (imputed) 0 burn http://www.ebi.ac.uk/efo/EFO_0009516 GCST90041722 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Foreign body injury (PheCode 1001) 1,124 European ancestry cases, 455,224 European ancestry controls NA NR [11842647] (imputed) 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90041723 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Coffee consumed (UKB data field 100240) 45,146 European ancestry cases, 18,855 European ancestry controls NA NR [11842647] (imputed) 0 coffee consumption http://www.ebi.ac.uk/efo/EFO_0004330 GCST90041724 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Added milk to instant coffee (UKB data field 100260) 64,001 European ancestry individuals NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041725 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Added milk to filtered coffee (UKB data field 100280) 8,378 European ancestry cases, 55,623 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041726 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Symptoms concerning nutrition, metabolism, and development (PheCode 1002) 1,482 European ancestry cases, 454,866 European ancestry controls NA NR [11842647] (imputed) 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90041727 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Decaffeinated coffee (UKB data field 100360) 7,241 European ancestry cases, 56,760 European ancestry controls NA NR [11842647] (imputed) 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90041728 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Tea consumed (UKB data field 100390) 50,994 European ancestry cases, 13,007 European ancestry controls NA NR [11842647] (imputed) 0 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST90041729 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Added milk to standard tea (UKB data field 100460) 41,684 European ancestry cases, 22,317 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041730 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcohol consumed (UKB data field 100580) 31,460 European ancestry cases, 32,541 European ancestry controls NA NR [11842647] (imputed) 0 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST90041731 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Other symptoms (PheCode 1005) 385 European ancestry cases, 455,963 European ancestry controls NA NR [11842647] (imputed) 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90041732 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Crushing injury (PheCode 1006) 186 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 crush injury http://www.ebi.ac.uk/efo/EFO_0009504 GCST90041733 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breakfast cereal consumed (UKB data field 100760) 42,090 European ancestry cases, 21,911 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041734 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Milk added to cereal (UKB data field 100890) 64,001 European ancestry individuals NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041735 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Crushing or internal injury to organs (PheCode 1008) 536 European ancestry cases, 455,812 European ancestry controls NA NR [11842647] (imputed) 0 heart injury http://www.ebi.ac.uk/efo/EFO_0009506 GCST90041736 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: did not have milk (UKB data field 100920_0) 3,262 European ancestry cases, 60,739 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041737 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: semiskimmed (UKB data field 100920_2102) 39,621 European ancestry cases, 24,380 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041738 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: skimmed (UKB data field 100920_2103) 13,045 European ancestry cases, 50,956 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041739 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: wholemilk (UKB data field 100920_2104) 3,644 European ancestry cases, 60,357 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041740 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: soya with calcium (UKB data field 100920_2105) 1,977 European ancestry cases, 62,024 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041741 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: soya without calcium (UKB data field 100920_2106) 851 European ancestry cases, 63,150 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041742 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: goat/sheep milk (UKB data field 100920_2107) 396 European ancestry cases, 63,605 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041743 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: rice/oat/vegetable milk (UKB data field 100920_2108) 368 European ancestry cases, 63,633 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041744 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Type milk consumed: powdered milk (UKB data field 100920_2109) 286 European ancestry cases, 63,715 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041745 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - paroxetine (UKB data field 20003_1140867888) 1,529 European ancestry cases, 454,747 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042042 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - amitriptyline hydrochloride+perphenazine 10mg/2mg tablet (UKB data field 20003_1140867948) 102 European ancestry cases, 456,174 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042043 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - motilium 10mg tablet (UKB data field 20003_1140867998) 143 European ancestry cases, 456,133 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042044 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - serc-8 tablet (UKB data field 20003_1140868064) 124 European ancestry cases, 456,152 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042045 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cyclizine (UKB data field 20003_1140868080) 166 European ancestry cases, 456,110 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042046 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - prochlorperazine (UKB data field 20003_1140868170) 634 European ancestry cases, 455,642 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042047 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - stemetil 5mg tablet (UKB data field 20003_1140868172) 277 European ancestry cases, 455,999 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042048 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - buccastem 3mg tablet (UKB data field 20003_1140868192) 119 European ancestry cases, 456,157 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042049 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - aspirin (UKB data field 20003_1140868226) 60,848 European ancestry cases, 395,428 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042050 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - prednisone (UKB data field 20003_1140868364) 277 European ancestry cases, 455,999 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042051 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - climaval 1mg tablet (UKB data field 20003_1140868372) 565 European ancestry cases, 246,943 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042052 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - premarin 625micrograms tablet (UKB data field 20003_1140868408) 1,904 European ancestry cases, 245,604 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042053 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - triamcinolone (UKB data field 20003_1140868426) 159 European ancestry cases, 456,117 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042054 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - oestradiol product (UKB data field 20003_1140868456) 104 European ancestry cases, 247,404 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042055 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hormonin tablet (UKB data field 20003_1140868458) 176 European ancestry cases, 247,332 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042056 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - progynova 1mg tablet (UKB data field 20003_1140868460) 190 European ancestry cases, 456,086 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042057 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vagifem 25mcg pessary (UKB data field 20003_1140868472) 1,246 European ancestry cases, 246,262 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042058 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tibolone (UKB data field 20003_1140868482) 784 European ancestry cases, 246,724 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042059 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nuvelle tablet (UKB data field 20003_1140868518) 194 European ancestry cases, 247,314 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042060 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - testosterone product (UKB data field 20003_1140868532) 281 European ancestry cases, 455,995 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042061 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - finasteride (UKB data field 20003_1140868550) 1,557 European ancestry cases, 454,719 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042062 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - norethisterone (UKB data field 20003_1140868580) 262 European ancestry cases, 247,246 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042063 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - progesterone product (UKB data field 20003_1140868588) 154 European ancestry cases, 247,354 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042064 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - didronel 200mg tablet (UKB data field 20003_1140868772) 152 European ancestry cases, 456,124 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042065 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - desmopressin (UKB data field 20003_1140868816) 113 European ancestry cases, 456,163 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042066 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Neoplasm of unspecified nature of digestive system (PheCode 158) 976 European ancestry cases, 455,372 European ancestry controls NA NR [11842647] (imputed) 0 digestive system neoplasm http://www.ebi.ac.uk/efo/EFO_0008549 GCST90041815 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of small intestine, including duodenum (PheCode 159.2) 172 European ancestry cases, 456,176 European ancestry controls NA NR [11842647] (imputed) 0 small intestine cancer http://purl.obolibrary.org/obo/MONDO_0000956 GCST90041816 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of gallbladder and extrahepatic bile ducts (PheCode 159.3) 195 European ancestry cases, 456,153 European ancestry controls NA NR [11842647] (imputed) 0 carcinoma of gallbladder and extrahepatic biliary tract http://purl.obolibrary.org/obo/MONDO_0018918 GCST90041817 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of retroperitoneum and peritoneum (PheCode 159.4) 186 European ancestry cases, 456,162 European ancestry controls NA NR [11842647] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90041818 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of other and ill-defined sites within the digestive organs and peritoneum (PheCode 159) 123 European ancestry cases, 456,225 European ancestry controls NA NR [11842647] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90041819 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Alcohol usually taken with meals (UKB data field 1618) 156,663 European ancestry cases, 75,922 European ancestry controls NA NR [11842647] (imputed) 0 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST90041820 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of bronchus; lung (PheCode 165.1) 2,120 European ancestry cases, 454,228 European ancestry controls NA NR [11842647] (imputed) 0 lung cancer, bronchus cancer http://purl.obolibrary.org/obo/MONDO_0008903, http://purl.obolibrary.org/obo/MONDO_0001672 GCST90041821 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer within the respiratory system (PheCode 165) 213 European ancestry cases, 456,135 European ancestry controls NA NR [11842647] (imputed) 0 respiratory system cancer http://purl.obolibrary.org/obo/MONDO_0000376 GCST90041822 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Breastfed as a baby (UKB data field 1677) 247,160 European ancestry cases, 99,661 European ancestry controls NA NR [11842647] (imputed) 0 social environment measurement http://www.ebi.ac.uk/efo/EFO_0010552 GCST90041823 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: oesophageal cancer (UKB data field 20001_1017) 196 European ancestry cases, 456,080 European ancestry controls NA NR [11842647] (imputed) 0 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST90041891 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: stomach cancer (UKB data field 20001_1018) 168 European ancestry cases, 456,108 European ancestry controls NA NR [11842647] (imputed) 0 stomach neoplasm http://www.ebi.ac.uk/efo/EFO_0003897 GCST90041892 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: small intestine/small bowel cancer (UKB data field 20001_1019) 208 European ancestry cases, 456,068 European ancestry controls NA NR [11842647] (imputed) 0 small intestine carcinoma http://www.ebi.ac.uk/efo/EFO_0005588 GCST90041893 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: large bowel cancer/colorectal cancer (UKB data field 20001_1020) 636 European ancestry cases, 455,640 European ancestry controls NA NR [11842647] (imputed) 0 colorectal carcinoma http://www.ebi.ac.uk/efo/EFO_1001951 GCST90041894 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: colon cancer/sigmoid cancer (UKB data field 20001_1022) 1,482 European ancestry cases, 454,794 European ancestry controls NA NR [11842647] (imputed) 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90041895 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: rectal cancer (UKB data field 20001_1023) 326 European ancestry cases, 455,950 European ancestry controls NA NR [11842647] (imputed) 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90041896 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: liver/hepatocellular cancer (UKB data field 20001_1024) 165 European ancestry cases, 456,111 European ancestry controls NA NR [11842647] (imputed) 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90041897 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: eye and/or adnexal cancer (UKB data field 20001_1030) 135 European ancestry cases, 456,141 European ancestry controls NA NR [11842647] (imputed) 0 eye neoplasm http://www.ebi.ac.uk/efo/EFO_0003824 GCST90041898 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: brain cancer / primary malignant brain tumour (UKB data field 20001_1032) 206 European ancestry cases, 456,070 European ancestry controls NA NR [11842647] (imputed) 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90041899 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: kidney/renal cell cancer (UKB data field 20001_1034) 600 European ancestry cases, 455,676 European ancestry controls NA NR [11842647] (imputed) 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90041900 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: bladder cancer (UKB data field 20001_1035) 1,090 European ancestry cases, 455,186 European ancestry controls NA NR [11842647] (imputed) 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90041901 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: ovarian cancer (UKB data field 20001_1039) 779 European ancestry cases, 246,729 European ancestry controls NA NR [11842647] (imputed) 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90041902 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: uterine/endometrial cancer (UKB data field 20001_1040) 1,143 European ancestry cases, 246,365 European ancestry controls NA NR [11842647] (imputed) 0 uterine carcinoma http://www.ebi.ac.uk/efo/EFO_0002919 GCST90041903 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: cervical cancer (UKB data field 20001_1041) 1,866 European ancestry cases, 245,642 European ancestry controls NA NR [11842647] (imputed) 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90041904 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: prostate cancer (UKB data field 20001_1044) 3,221 European ancestry cases, 205,547 European ancestry controls NA NR [11842647] (imputed) 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90041905 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: testicular cancer (UKB data field 20001_1045) 797 European ancestry cases, 207,971 European ancestry controls NA NR [11842647] (imputed) 0 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST90041906 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: lymphoma (UKB data field 20001_1047) 118 European ancestry cases, 456,158 European ancestry controls NA NR [11842647] (imputed) 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90041907 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: leukaemia (UKB data field 20001_1048) 207 European ancestry cases, 456,069 European ancestry controls NA NR [11842647] (imputed) 0 leukemia http://www.ebi.ac.uk/efo/EFO_0000565 GCST90041908 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: multiple myeloma (UKB data field 20001_1050) 163 European ancestry cases, 456,113 European ancestry controls NA NR [11842647] (imputed) 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90041909 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: hodgkins lymphoma / hodgkins disease (UKB data field 20001_1052) 429 European ancestry cases, 455,847 European ancestry controls NA NR [11842647] (imputed) 0 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST90041910 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: non-hodgkins lymphoma (UKB data field 20001_1053) 883 European ancestry cases, 455,393 European ancestry controls NA NR [11842647] (imputed) 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90041911 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: chronic lymphocytic (UKB data field 20001_1055) 300 European ancestry cases, 455,976 European ancestry controls NA NR [11842647] (imputed) 0 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90041912 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: chronic myeloid (UKB data field 20001_1056) 112 European ancestry cases, 456,164 European ancestry controls NA NR [11842647] (imputed) 0 chronic myelogenous leukemia http://www.ebi.ac.uk/efo/EFO_0000339 GCST90041913 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: malignant melanoma (UKB data field 20001_1059) 3,564 European ancestry cases, 452,712 European ancestry controls NA NR [11842647] (imputed) 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90041914 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: non-melanoma skin cancer (UKB data field 20001_1060) 665 European ancestry cases, 455,611 European ancestry controls NA NR [11842647] (imputed) 0 non-melanoma skin carcinoma http://www.ebi.ac.uk/efo/EFO_0009260 GCST90041915 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: basal cell carcinoma (UKB data field 20001_1061) 4,257 European ancestry cases, 452,019 European ancestry controls NA NR [11842647] (imputed) 0 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90041916 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: squamous cell carcinoma (UKB data field 20001_1062) 557 European ancestry cases, 455,719 European ancestry controls NA NR [11842647] (imputed) 0 squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707 GCST90041917 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: primary bone cancer (UKB data field 20001_1063) 127 European ancestry cases, 456,149 European ancestry controls NA NR [11842647] (imputed) 0 bone neoplasm http://www.ebi.ac.uk/efo/EFO_0003820 GCST90041918 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: thyroid cancer (UKB data field 20001_1065) 422 European ancestry cases, 455,854 European ancestry controls NA NR [11842647] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90041919 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: sarcoma/fibrosarcoma (UKB data field 20001_1068) 235 European ancestry cases, 456,041 European ancestry controls NA NR [11842647] (imputed) 0 sarcoma, fibrosarcoma http://www.ebi.ac.uk/efo/EFO_0000691, http://www.ebi.ac.uk/efo/EFO_0002087 GCST90041920 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: malignant lymph node, unspecified (UKB data field 20001_1070) 121 European ancestry cases, 456,155 European ancestry controls NA NR [11842647] (imputed) 0 lymphoid neoplasm http://www.ebi.ac.uk/efo/EFO_0001642 GCST90041921 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: cin/pre-cancer cells cervix (UKB data field 20001_1072) 1,577 European ancestry cases, 245,931 European ancestry controls NA NR [11842647] (imputed) 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90041922 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: rodent ulcer (UKB data field 20001_1073) 633 European ancestry cases, 455,643 European ancestry controls NA NR [11842647] (imputed) 0 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90041923 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer code, self-reported: unclassifiable (UKB data field 20001_99999) 505 European ancestry cases, 455,771 European ancestry controls NA NR [11842647] (imputed) 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90041924 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - senokot 7.5mg tablet (UKB data field 20003_1140851088) 189 European ancestry cases, 456,087 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041925 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - gtn 400micrograms spray (UKB data field 20003_1140851812) 1,085 European ancestry cases, 455,191 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041926 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin a (UKB data field 20003_1140852756) 152 European ancestry cases, 456,124 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041927 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcium+vitamin d 500units tablet (UKB data field 20003_1140852948) 1,973 European ancestry cases, 454,303 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041928 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - multivitamins (UKB data field 20003_1140852976) 13,991 European ancestry cases, 442,285 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041929 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - macrogol ointment (UKB data field 20003_1140854076) 103 European ancestry cases, 456,173 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041930 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - syndol tablet (UKB data field 20003_1140856342) 350 European ancestry cases, 455,926 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041931 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bread type: Other type of bread (UKB data field 1448_4) 18,585 European ancestry cases, 421,499 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041790 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of tongue (PheCode 145.2) 322 European ancestry cases, 456,026 European ancestry controls NA NR [11842647] (imputed) 0 tongue neoplasm http://www.ebi.ac.uk/efo/EFO_0003871 GCST90041791 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of major salivary glands (PheCode 145.3) 105 European ancestry cases, 456,243 European ancestry controls NA NR [11842647] (imputed) 0 Major Salivary Gland Carcinoma http://www.ebi.ac.uk/efo/EFO_1000344 GCST90041792 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of mouth (PheCode 145) 156 European ancestry cases, 456,192 European ancestry controls NA NR [11842647] (imputed) 0 oral cavity cancer http://www.ebi.ac.uk/efo/EFO_0005570 GCST90041793 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cereal type: Bran cereal (e.g. All Bran, Branflakes) (UKB data field 1468_1) 63,677 European ancestry cases, 314,124 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041794 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cereal type: Biscuit cereal (e.g. Weetabix) (UKB data field 1468_2) 67,149 European ancestry cases, 310,652 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041795 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cereal type: Oat cereal (e.g. Ready Brek, porridge) (UKB data field 1468_3) 96,498 European ancestry cases, 281,303 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041796 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cereal type: Muesli (UKB data field 1468_4) 76,991 European ancestry cases, 300,810 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041797 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cereal type: Other (e.g. Cornflakes, Frosties) (UKB data field 1468_5) 73,486 European ancestry cases, 304,315 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041798 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of oropharynx (PheCode 149.1) 270 European ancestry cases, 456,078 European ancestry controls NA NR [11842647] (imputed) 0 tonsil cancer http://www.ebi.ac.uk/efo/EFO_1001214 GCST90041799 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of larynx (PheCode 149.4) 269 European ancestry cases, 456,079 European ancestry controls NA NR [11842647] (imputed) 0 Malignant Laryngeal Neoplasm http://www.ebi.ac.uk/efo/EFO_1000354 GCST90041800 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Coffee type: Decaffeinated coffee (any type) (UKB data field 1508_1) 69,306 European ancestry cases, 288,119 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041801 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Coffee type: Instant coffee (UKB data field 1508_2) 200,087 European ancestry cases, 157,338 European ancestry controls NA NR [11842647] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041802 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Coffee type: Ground coffee (include espresso, filter etc) (UKB data field 1508_3) 81,903 European ancestry cases, 275,522 European ancestry controls NA NR [11842647] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041803 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Coffee type: Other type of coffee (UKB data field 1508_4) 6,129 European ancestry cases, 351,296 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041804 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of esophagus (PheCode 150) 750 European ancestry cases, 455,598 European ancestry controls NA NR [11842647] (imputed) 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90041805 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of stomach (PheCode 151) 569 European ancestry cases, 455,779 European ancestry controls NA NR [11842647] (imputed) 0 stomach neoplasm http://www.ebi.ac.uk/efo/EFO_0003897 GCST90041806 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Colon cancer (PheCode 153.2) 3,221 European ancestry cases, 453,127 European ancestry controls NA NR [11842647] (imputed) 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90041807 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of rectum, rectosigmoid junction, and anus (PheCode 153.3) 2,202 European ancestry cases, 454,146 European ancestry controls NA NR [11842647] (imputed) 0 rectosigmoid junction neoplasm http://purl.obolibrary.org/obo/MONDO_0002423 GCST90041808 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Major dietary changes in the last 5 years: No (UKB data field 1538_0) 279,134 European ancestry cases, 176,043 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041809 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Major dietary changes in the last 5 years: Yes, because of illness (UKB data field 1538_1) 48,347 European ancestry cases, 406,830 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041810 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Major dietary changes in the last 5 years: Yes, because of other reasons (UKB data field 1538_2) 127,696 European ancestry cases, 327,481 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041811 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Malignant neoplasm of liver, primary (PheCode 155.1) 128 European ancestry cases, 456,220 European ancestry controls NA NR [11842647] (imputed) 0 liver cancer http://purl.obolibrary.org/obo/MONDO_0002691 GCST90041812 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Cancer of liver and intrahepatic bile duct (PheCode 155) 214 European ancestry cases, 456,134 European ancestry controls NA NR [11842647] (imputed) 0 liver neoplasm http://www.ebi.ac.uk/efo/EFO_1001513 GCST90041813 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Pancreatic cancer (PheCode 157) 587 European ancestry cases, 455,761 European ancestry controls NA NR [11842647] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90041814 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin b compound tablet (UKB data field 20003_1140871024) 3,269 European ancestry cases, 453,007 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042092 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcichew d3 tablet (UKB data field 20003_1140871050) 4,421 European ancestry cases, 451,855 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042093 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcium carbonate+cholecalciferol 1.25g/5micrograms tablet (UKB data field 20003_1140871052) 187 European ancestry cases, 456,089 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042094 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin e product (UKB data field 20003_1140871112) 1,707 European ancestry cases, 454,569 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042095 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Vitamin supplement user (UKB data field 104670) 26,193 European ancestry cases, 37,808 European ancestry controls NA NR [11842647] (imputed) 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90041769 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Invitation to physical activity study, acceptance (UKB data field 110005) 217,653 European ancestry individuals NA NR [11842647] (imputed) 0 physical activity http://www.ebi.ac.uk/efo/EFO_0003940 GCST90041770 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Candidiasis (PheCode 112) 417 European ancestry cases, 455,931 European ancestry controls NA NR [11842647] (imputed) 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90041771 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Usual side of head for mobile phone use: Left (UKB data field 1150_1) 136,443 European ancestry cases, 246,837 European ancestry controls NA NR [11842647] (imputed) 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90041772 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Usual side of head for mobile phone use: Right (UKB data field 1150_2) 221,755 European ancestry cases, 161,525 European ancestry controls NA NR [11842647] (imputed) 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90041773 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Usual side of head for mobile phone use: Equally left and right (UKB data field 1150_3) 25,082 European ancestry cases, 358,198 European ancestry controls NA NR [11842647] (imputed) 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90041774 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Snoring (UKB data field 1210) 266,211 European ancestry cases, 158,178 European ancestry controls NA NR [11842647] (imputed) 0 snoring measurement http://www.ebi.ac.uk/efo/EFO_0008341 GCST90041775 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Arthropod-borne diseases (PheCode 133) 66 European ancestry cases, 456,282 European ancestry controls NA NR [11842647] (imputed) 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90041776 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Milk type used: Full cream (UKB data field 1418_1) 29,211 European ancestry cases, 426,605 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041777 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Milk type used: Semi-skimmed (UKB data field 1418_2) 296,081 European ancestry cases, 159,735 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041778 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Milk type used: Skimmed (UKB data field 1418_3) 93,232 European ancestry cases, 362,584 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041779 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Milk type used: Soya (UKB data field 1418_4) 16,947 European ancestry cases, 438,869 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041780 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Milk type used: Other type of milk (UKB data field 1418_5) 5,437 European ancestry cases, 450,379 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041781 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Milk type used: Never/rarely have milk (UKB data field 1418_6) 14,908 European ancestry cases, 440,908 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041782 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spread type: Never/rarely use spread (UKB data field 1428_0) 47,226 European ancestry cases, 407,942 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041783 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spread type: Butter/spreadable butter (UKB data field 1428_1) 166,328 European ancestry cases, 288,840 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041784 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spread type: Flora Pro-Active/Benecol (UKB data field 1428_2) 2,383 European ancestry cases, 452,785 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041785 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Spread type: Other type of spread/margarine (UKB data field 1428_3) 239,231 European ancestry cases, 215,937 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041786 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bread type: White (UKB data field 1448_1) 115,996 European ancestry cases, 324,088 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041787 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bread type: Brown (UKB data field 1448_2) 52,852 European ancestry cases, 387,232 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041788 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Bread type: Wholemeal or wholegrain (UKB data field 1448_3) 252,651 European ancestry cases, 187,433 European ancestry controls NA NR [11842647] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90041789 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - depo-provera 50mg/1ml injection (UKB data field 20003_1140857620) 331 European ancestry cases, 247,177 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041932 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - prempak 0.625 tablet (UKB data field 20003_1140857636) 679 European ancestry cases, 246,829 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041933 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hepacon b12 1mg/1ml injection (UKB data field 20003_1140858452) 196 European ancestry cases, 456,080 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041934 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - cardura 1mg tablet (UKB data field 20003_1140860690) 229 European ancestry cases, 456,047 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041935 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lisinopril (UKB data field 20003_1140860696) 12,644 European ancestry cases, 443,632 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041936 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - quinapril (UKB data field 20003_1140860728) 197 European ancestry cases, 456,079 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041937 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - captopril (UKB data field 20003_1140860750) 197 European ancestry cases, 456,079 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041938 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - enalapril maleate+hydrochlorothiazide 20mg/12.5mg tablet (UKB data field 20003_1140860790) 123 European ancestry cases, 456,153 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041939 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - coversyl 2mg tablet (UKB data field 20003_1140860802) 150 European ancestry cases, 456,126 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041940 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ramipril (UKB data field 20003_1140860806) 21,181 European ancestry cases, 435,095 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041941 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - glyceryl trinitrate (UKB data field 20003_1140860834) 1,397 European ancestry cases, 454,879 European ancestry controls NA NR [11842647] (imputed) 1 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041942 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nitrolingual 400micrograms spray (UKB data field 20003_1140860840) 470 European ancestry cases, 455,806 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041943 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - trandolapril (UKB data field 20003_1140860904) 257 European ancestry cases, 456,019 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041944 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - isosorbide mononitrate (UKB data field 20003_1140860954) 1,511 European ancestry cases, 454,765 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041945 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - imdur 60mg durule (UKB data field 20003_1140860976) 168 European ancestry cases, 456,108 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041946 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - isosorbide dinitrate (UKB data field 20003_1140861008) 104 European ancestry cases, 456,172 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041947 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - nifedipine (UKB data field 20003_1140861088) 1,020 European ancestry cases, 455,256 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041948 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - adalat 5mg capsule (UKB data field 20003_1140861090) 1,045 European ancestry cases, 455,231 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041949 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - coracten sr 10mg m/r capsule (UKB data field 20003_1140861120) 394 European ancestry cases, 455,882 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041950 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tildiem 60mg m/r tablet (UKB data field 20003_1140861128) 851 European ancestry cases, 455,425 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041951 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - adizem-60 m/r tablet (UKB data field 20003_1140861138) 416 European ancestry cases, 455,860 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041952 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dilzem sr 60mg long acting m/r capsule (UKB data field 20003_1140861166) 194 European ancestry cases, 456,082 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041953 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - istin 5mg tablet (UKB data field 20003_1140861202) 142 European ancestry cases, 456,134 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041954 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - lacidipine (UKB data field 20003_1140861276) 474 European ancestry cases, 455,802 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041955 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - dipyridamole (UKB data field 20003_1140861778) 822 European ancestry cases, 455,454 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90041956 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ortho-gynest 500micrograms pessary (UKB data field 20003_1140869034) 353 European ancestry cases, 247,155 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042067 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ovestin 0.1% vaginal cream (UKB data field 20003_1140869036) 317 European ancestry cases, 247,191 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042068 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - marvelon tablet (UKB data field 20003_1140869162) 109 European ancestry cases, 247,399 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042069 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - mercilon tablet (UKB data field 20003_1140869164) 136 European ancestry cases, 247,372 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042070 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - logynon tablet (UKB data field 20003_1140869176) 183 European ancestry cases, 247,325 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042071 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - microgynon 30 tablet (UKB data field 20003_1140869180) 668 European ancestry cases, 246,840 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042072 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - micronor tablet (UKB data field 20003_1140869276) 652 European ancestry cases, 246,856 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042073 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - noriday tablet (UKB data field 20003_1140869278) 342 European ancestry cases, 247,166 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042074 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - femulen tablet (UKB data field 20003_1140869362) 363 European ancestry cases, 247,145 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042075 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - norgeston tablet (UKB data field 20003_1140869370) 141 European ancestry cases, 247,367 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042076 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - methotrexate (UKB data field 20003_1140869848) 2,422 European ancestry cases, 453,854 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042077 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - azathioprine (UKB data field 20003_1140869930) 946 European ancestry cases, 455,330 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042078 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - tamoxifen (UKB data field 20003_1140870164) 1,422 European ancestry cases, 454,854 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042079 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - zoladex 3.6mg implant (UKB data field 20003_1140870196) 247 European ancestry cases, 456,029 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042080 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - iron+folic acid (UKB data field 20003_1140870306) 215 European ancestry cases, 456,061 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042081 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - ferrous sulphate (UKB data field 20003_1140870390) 2,268 European ancestry cases, 454,008 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042082 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - folic acid product (UKB data field 20003_1140870422) 3,819 European ancestry cases, 452,457 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042083 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - forceval capsule (UKB data field 20003_1140870488) 125 European ancestry cases, 456,151 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042084 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - hydroxocobalamin product (UKB data field 20003_1140870504) 106 European ancestry cases, 456,170 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042085 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin b12 preparation (UKB data field 20003_1140870570) 1,394 European ancestry cases, 454,882 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042086 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcium salts (UKB data field 20003_1140870788) 2,785 European ancestry cases, 453,491 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042087 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcichew 1.25g chewable tablet (UKB data field 20003_1140870856) 984 European ancestry cases, 455,292 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042088 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - calcichew forte 2.5g chewable tablet (UKB data field 20003_1140870862) 454 European ancestry cases, 455,822 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042089 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - vitamin d product (UKB data field 20003_1140870954) 1,228 European ancestry cases, 455,048 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042090 Genome-wide genotyping array 2021-12-01 34737426 Jiang L 2021-11-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34737426 A generalized linear mixed model association tool for biobank-scale data. Treatment or medication use - alfacalcidol (UKB data field 20003_1140870956) 383 European ancestry cases, 455,893 European ancestry controls NA NR [11842647] (imputed) 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90042091 Genome-wide genotyping array 2022-05-05 35013560 Chamnanphon M 2022-01-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35013560 Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population. COVID-19 191 Thai ancestry cases, 31 Thai ancestry controls NA Affymetrix [558132] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90101761 Genome-wide genotyping array 2022-05-05 35013560 Chamnanphon M 2022-01-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35013560 Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population. COVID-19 severity (moderate-severe vs mild) 66 Thai ancestry cases, 125 Thai ancestry controls NA Affymetrix [558132] (imputed) 1 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90101762 Genome-wide genotyping array 2022-05-05 35013560 Chamnanphon M 2022-01-11 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35013560 Host genetic factors of COVID-19 susceptibility and disease severity in a Thai population. COVID-19 severity 191 Thai ancestry individuals NA Affymetrix [558132] (imputed) 1 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90101763 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C36:5 levels 16,835 Caucasian ancestry individuals NA Affymetrix, Illumina [5790837] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010804 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C36:6 levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5791314] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010805 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C38:0 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791519] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010806 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C38:3 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791226] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010807 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C38:4 levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5791386] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010808 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C38:5 levels 16,836 Caucasian ancestry individuals NA Affymetrix, Illumina [5791436] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010809 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C38:6 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791244] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010810 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C40:2 levels 16,719 Caucasian ancestry individuals NA Affymetrix, Illumina [5793499] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010811 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C40:3 levels 16,431 Caucasian ancestry individuals NA Affymetrix, Illumina [5793014] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010812 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C30:0 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791235] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010792 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C32:0 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791755] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010793 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C32:1 levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5790467] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010794 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C32:2 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5789893] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010795 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C34:1 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791930] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010796 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C34:2 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792223] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010797 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C34:3 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791551] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010798 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C34:4 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5790991] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010799 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C36:0 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791651] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010800 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C36:2 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792013] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010801 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C36:3 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791858] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010802 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C36:4 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791936] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010803 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C40:4 levels 16,835 Caucasian ancestry individuals NA Affymetrix, Illumina [5791955] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010813 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C40:5 levels 16,835 Caucasian ancestry individuals NA Affymetrix, Illumina [5791407] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010814 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C40:6 levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5791022] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010815 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C42:0 levels 16,118 Caucasian ancestry individuals NA Affymetrix, Illumina [5791949] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010816 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C42:4 levels 16,611 Caucasian ancestry individuals NA Affymetrix, Illumina [5793588] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010818 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C42:5 levels 16,508 Caucasian ancestry individuals NA Affymetrix, Illumina [5792227] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010819 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C42:6 levels 15,749 Caucasian ancestry individuals NA Affymetrix, Illumina [6084545] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010820 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C30:1 levels 9,003 Caucasian ancestry individuals NA Affymetrix, Illumina [6083739] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010821 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C30:2 levels 9,286 Caucasian ancestry individuals NA Affymetrix, Illumina [6083559] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010822 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C32:1 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791633] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010823 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C32:2 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792117] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010824 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C34:1 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791726] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010825 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C34:2 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791125] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010826 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C34:3 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5790966] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010827 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C36:2 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791425] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010828 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C36:3 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791531] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010829 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C36:4 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791467] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010830 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C36:5 levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5791674] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010831 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C38:0 levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5791382] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010832 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C38:1 levels 15,899 Caucasian ancestry individuals NA Affymetrix, Illumina [6085896] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010833 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C38:2 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792947] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010834 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C38:3 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5792424] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010835 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C38:4 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791693] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010836 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C38:5 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791842] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010837 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C38:6 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791449] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010838 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Ornithine levels 30,920 Caucasian ancestry individuals NA Affymetrix, Illumina [6046416] (imputed) 7 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90010735 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C24:0 levels 13,184 Caucasian ancestry individuals NA Affymetrix, Illumina [6083416] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010789 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C26:0 levels 9,363 Caucasian ancestry individuals NA Affymetrix, Illumina [6083682] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010790 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C28:1 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791678] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010791 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024434 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024435 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024436 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024437 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024438 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:6) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024439 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:6) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024440 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-19:0/20:4) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024441 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-19:0/20:4) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024442 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024443 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024444 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024445 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024446 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:1/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024447 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:1/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024448 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (34:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90024449 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (34:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90024450 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (36:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90024451 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (36:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90024452 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_20:4) levels/Phosphatidylinositol (17:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024453 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024454 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_16:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024455 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024456 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024457 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024458 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/20:4) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024409 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/20:4) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024410 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/22:6) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024411 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/22:6) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024412 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024413 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024414 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024415 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 21 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024416 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024417 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024418 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024419 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024420 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:5) (n3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024421 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:5) (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024422 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024423 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024424 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:1) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024425 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:1) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024426 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:2) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024427 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:2) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024428 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024429 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 15 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024430 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024431 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:4) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024432 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:4) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024433 Genome-wide genotyping array 2022-04-11 34992631 Armstrong ND 2021-12-21 Front Genet www.ncbi.nlm.nih.gov/pubmed/34992631 Genetic Contributors of Incident Stroke in 10,700 African Americans With Hypertension: A Meta-Analysis From the Genetics of Hypertension Associated Treatments and Reasons for Geographic and Racial Differences in Stroke Studies. Incident stroke in hypertension 646 African American cases, 10,071 African American controls 145 African American cases, 645 African American controls Illumina [20575549] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90101797 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 88 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092954 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 109 triglycerides:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092955 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 62 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092956 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 42 cholesterol:total lipids ratio, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092957 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 63 cholesteryl ester measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092958 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 57 low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90092959 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 63 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092960 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 97 low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90092961 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 66 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092962 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of small LDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 64 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092963 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 69 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092964 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 61 low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90092965 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 90 triglyceride measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092966 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in small LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 88 triglycerides:total lipids ratio, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092967 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 71 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092968 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 82 very low density lipoprotein cholesterol measurement, cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020943 GCST90092969 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 75 cholesteryl ester measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092970 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 80 very low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90092971 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 64 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092972 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 93 very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90092973 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 89 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092974 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of small VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 87 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092975 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 73 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092976 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 89 very low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90092977 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 99 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092978 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024036 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024037 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024038 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024039 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024040 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024041 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024042 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024043 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024044 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024045 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024046 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024047 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/26:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024048 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024049 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024050 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/17:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024051 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024052 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024053 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024054 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024055 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024056 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/26:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024057 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024058 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024059 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 16 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024060 Genome-wide genotyping array 2022-03-03 34734498 Xhaard C 2021-11-03 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/34734498 Impact of natriuretic peptide polymorphisms on diastolic and metabolic function in a populational cohort: insights from the STANISLAS cohort. N-terminal prohormone brain natriuretic peptide levels 1,555 French ancestry individuals from 664 families NA Illumina [520773] 1 N-terminal prohormone brain natriuretic peptide measurement http://www.ebi.ac.uk/efo/EFO_0010921 GCST90095077 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (16:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90025444 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (17:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021465 GCST90025445 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (17:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021465 GCST90025446 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90025447 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90025448 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:1) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90025449 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:1) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90025450 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:2) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90025451 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:2) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90025452 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (20:4) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90025453 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (20:4) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90025454 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (22:6) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90025455 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (22:6) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90025456 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90025457 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90025458 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90025459 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90025460 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025461 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025462 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:1) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025463 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:1) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025464 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:2) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025465 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:2) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025466 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (20:4) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025467 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (20:4) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025468 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Oxidized cholesteryl ester (18:2) [+2O] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025469 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Oxidized cholesteryl ester (18:2) [+O] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025470 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025471 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025472 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025473 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025474 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025475 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025476 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025477 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025478 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025479 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025480 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025481 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025482 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (39:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024479 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (36:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024480 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (36:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024481 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024482 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024483 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024484 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (40:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024485 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (40:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024486 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (34:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024487 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (35:2) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024488 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (37:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024489 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:2) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90025394 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn1] (a) levels/Lysophosphatidylcholine (18:3) [sn2] (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90025395 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn1] levels (b) 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90025396 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn2] levels (a) 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90025397 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) (a) [sn1] [104_sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90025398 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn1] (a) levels / Lysophosphatidylcholine (19:0) [sn2] (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90025399 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn1] levels (b) 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90025400 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn2] levels (a) 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90025401 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021456 GCST90025402 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021456 GCST90025403 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:1) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90025404 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:1) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90025405 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:2) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021458 GCST90025406 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:2) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021458 GCST90025407 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:3) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90025408 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:3) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90025409 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:4) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90025410 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:4) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90025411 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:5) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90025412 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:5) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90025413 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021459 GCST90025414 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021459 GCST90025415 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:1) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021460 GCST90025416 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:1) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021460 GCST90025417 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:4) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90025418 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:4) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90025419 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn1] (n3) levels/Lysophosphatidylcholine (22:5) [sn2] (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90025420 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn1] (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90025421 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn2] (n3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90025422 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:6) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90025423 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:6) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90025424 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (24:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90025425 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (24:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90025426 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (26:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 26:0 measurement http://www.ebi.ac.uk/efo/EFO_0021464 GCST90025427 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (26:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 26:0 measurement http://www.ebi.ac.uk/efo/EFO_0021464 GCST90025428 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025429 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025430 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025431 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025432 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-20:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025433 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025434 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-22:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025435 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025436 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025437 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025438 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025439 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025440 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025441 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025442 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (16:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90025443 Genome-wide genotyping array 2022-04-05 34358307 Traylor M 2021-08-06 Brain www.ncbi.nlm.nih.gov/pubmed/34358307 The BS variant of C4 protects against age-related loss of white matter microstructural integrity. White matter fractional anisotropy x age interaction (2df) 31,125 British ancestry individuals NA NR [NR] (imputed) 7 white matter integrity, age at assessment http://www.ebi.ac.uk/efo/EFO_0004641, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90100584 Genome-wide genotyping array 2022-04-05 34358307 Traylor M 2021-08-06 Brain www.ncbi.nlm.nih.gov/pubmed/34358307 The BS variant of C4 protects against age-related loss of white matter microstructural integrity. White matter mean diffusivity x age interaction (2df) 31,128 British ancestry individuals NA NR [NR] (imputed) 22 white matter integrity, age at assessment http://www.ebi.ac.uk/efo/EFO_0004641, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90100583 Genome-wide genotyping array 2022-05-11 35094024 Zhou H 2022-01-29 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/35094024 Genome-wide meta-analysis of alcohol use disorder in East Asians. Alcohol use disorder 2,254 East Asian ancestry cases, 11,297 East Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 2 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90102554 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting insulin adjusted for BMI 48,395 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Other ancestry, Native American ancestry individuals NA Affymetrix, Illumina [28462191] (imputed) 11 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST90094952 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting insulin adjusted for BMI 19,525 European ancestry individuals NA Affymetrix, Illumina [28462191] (imputed) 0 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST90094953 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting insulin adjusted for BMI 10,755 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [28462191] (imputed) 0 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST90094954 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting insulin adjusted for BMI 14,425 Hispanic or Latin American individuals NA Affymetrix, Illumina [28462191] (imputed) 0 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST90094955 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting insulin adjusted for BMI 1,898 Asian ancestry individuals NA Affymetrix, Illumina [28462191] (imputed) 0 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST90094956 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting insulin adjusted for BMI 1,397 Other ancestry individuals NA Affymetrix, Illumina [28462191] (imputed) 0 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST90094957 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting insulin adjusted for BMI 395 Native American ancestry individuals NA Affymetrix, Illumina [28462191] (imputed) 0 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST90094958 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting glucose adjusted for BMI 52,211 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Other ancestry, Native American ancestry individuals NA Affymetrix, Illumina [29259056] (imputed) 14 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST90094959 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting glucose adjusted for BMI 19,745 European ancestry individuals NA Affymetrix, Illumina [29259056] (imputed) 13 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST90094960 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting glucose adjusted for BMI 12,195 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [29259056] (imputed) 5 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST90094961 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting glucose adjusted for BMI 16,018 Hispanic or Latin American individuals NA Affymetrix, Illumina [29259056] (imputed) 5 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST90094962 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting glucose adjusted for BMI 2,273 Asian ancestry individuals NA Affymetrix, Illumina [29259056] (imputed) 0 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST90094963 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting glucose adjusted for BMI 1,400 Other ancestry individuals NA Affymetrix, Illumina [29259056] (imputed) 0 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST90094964 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Fasting glucose adjusted for BMI 412 Native American ancestry individuals NA Affymetrix, Illumina [29259056] (imputed) 0 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST90094965 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Glycated haemoglobin HbA1c levels adjusted for BMI 23,357 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry individuals NA Affymetrix, Illumina [23060038] (imputed) 13 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90094966 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Glycated haemoglobin HbA1c levels adjusted for BMI 9,228 European ancestry individuals NA Affymetrix, Illumina [23060038] (imputed) 16 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90094967 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Glycated haemoglobin HbA1c levels adjusted for BMI 3,224 African American or Afro-Caribbean individuals NA Affymetrix, Illumina [23060038] (imputed) 3 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90094968 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Glycated haemoglobin HbA1c levels adjusted for BMI 10,693 Hispanic or Latin American individuals NA Affymetrix, Illumina [23060038] (imputed) 12 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90094969 Genome-wide genotyping array 2022-03-01 34951656 Downie CG 2021-12-24 Diabetologia www.ncbi.nlm.nih.gov/pubmed/34951656 Multi-ethnic GWAS and fine-mapping of glycaemic traits identify novel loci in the PAGE Study. Glycated haemoglobin HbA1c levels adjusted for BMI 92 Asian ancestry individuals NA Affymetrix, Illumina [23060038] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90094970 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025605 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025606 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025607 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025608 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025609 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:5) (n3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025610 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:5) (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025611 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (16:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024618 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (17:0) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024619 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (17:0) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024620 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024621 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 4 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024622 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024623 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (14:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010340 GCST90024624 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (15:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021434 GCST90024625 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90024626 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90024627 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 cholesteryl ester 16:2 measurement http://www.ebi.ac.uk/efo/EFO_0021435 GCST90024628 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (17:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021436 GCST90024629 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (17:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021437 GCST90024630 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90024631 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90024632 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90024633 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90024634 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021438 GCST90024635 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-20:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025580 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-36:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025581 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-38:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025582 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-38:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025583 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025584 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025585 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025586 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025587 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025588 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_16:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025589 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025590 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025591 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025592 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025593 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025594 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025595 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025596 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025597 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:1_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025598 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:1_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025599 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025600 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025601 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025602 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025603 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025604 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021439 GCST90024636 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021440 GCST90024637 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90024638 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90024639 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90024640 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021441 GCST90024641 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021442 GCST90024642 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021443 GCST90024643 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:5) (n3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90024644 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:5) (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90024645 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90024646 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021445 GCST90024647 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 24:1 measurement http://www.ebi.ac.uk/efo/EFO_0021446 GCST90024648 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester 24:4 measurement http://www.ebi.ac.uk/efo/EFO_0021447 GCST90024649 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester 24:5 measurement http://www.ebi.ac.uk/efo/EFO_0021448 GCST90024650 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester 24:6 measurement http://www.ebi.ac.uk/efo/EFO_0021449 GCST90024651 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024652 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024653 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024654 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024655 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024656 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024657 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024658 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024659 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024660 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-36:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025555 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-38:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025556 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025557 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:7) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025558 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:7) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025559 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-15:0/20:4) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025560 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-15:0/20:4) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025561 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025562 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025563 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/16:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025564 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025565 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025566 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025567 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025568 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025569 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025570 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025571 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-17:0/20:4) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025572 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-17:0/20:4) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025573 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025574 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025575 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/22:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025576 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025577 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:1/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025578 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:1/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025579 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024661 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024662 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024663 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024664 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024665 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024666 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024667 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024668 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/14:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024669 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024670 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024671 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024672 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024673 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024674 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024675 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/26:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024676 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/14:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024677 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025612 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025613 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025614 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_22:6) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025615 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_22:6) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025616 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (36:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025617 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (38:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025618 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (38:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025619 Genome-wide genotyping array 2022-05-13 35104449 John C 2022-01-29 Chest www.ncbi.nlm.nih.gov/pubmed/35104449 Genetic associations and architecture of asthma-chronic obstructive pulmonary disease overlap. Asthma-COPD overlap syndrome 8,068 European ancestry cases, 40,360 European ancestry controls 4,301 European ancestry cases, 48,609 European ancestry controls, 297 African American cases, 1,335 African American controls Affymetrix [7693381] (imputed) 22 asthma, chronic obstructive pulmonary disease http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0000341 GCST90102597 Genome-wide genotyping array 2022-12-02 33029326 Morey RA 2020-07-29 Eur J Psychotraumatol www.ncbi.nlm.nih.gov/pubmed/33029326 Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. Hippocampal R-fimbria volume in trauma-exposed individuals 83 European ancestry individuals, 74 African American or Afro-Caribbean individuals 79 African American or Afro-Caribbean post-traumatic stress disorder cases, 54 African American or Afro-Caribbean trauma-exposed controls Illumina [2711511] (imputed) 0 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST90239830 Genome-wide genotyping array 2022-12-02 33029326 Morey RA 2020-07-29 Eur J Psychotraumatol www.ncbi.nlm.nih.gov/pubmed/33029326 Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. Hippocampal L-fimbria volume in trauma-exposed individuals 83 European ancestry individuals, 74 African American or Afro-Caribbean individuals 79 African American or Afro-Caribbean post-traumatic stress disorder cases, 54 African American or Afro-Caribbean trauma-exposed controls Illumina [2711511] (imputed) 0 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST90239831 Genome-wide genotyping array 2022-12-02 33029326 Morey RA 2020-07-29 Eur J Psychotraumatol www.ncbi.nlm.nih.gov/pubmed/33029326 Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. Hippocampal R-subiculum volume in trauma-exposed individuals 83 European ancestry individuals, 74 African American or Afro-Caribbean individuals 79 African American or Afro-Caribbean post-traumatic stress disorder cases, 54 African American or Afro-Caribbean trauma-exposed controls Illumina [2711511] (imputed) 0 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90239832 Genome-wide genotyping array 2022-12-02 33029326 Morey RA 2020-07-29 Eur J Psychotraumatol www.ncbi.nlm.nih.gov/pubmed/33029326 Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. Hippocampal L-CA1 volume in trauma-exposed individuals 83 European ancestry individuals, 74 African American or Afro-Caribbean individuals 79 African American or Afro-Caribbean post-traumatic stress disorder cases, 54 African American or Afro-Caribbean trauma-exposed controls Illumina [2711511] (imputed) 0 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90239833 Genome-wide genotyping array 2022-12-02 33029326 Morey RA 2020-07-29 Eur J Psychotraumatol www.ncbi.nlm.nih.gov/pubmed/33029326 Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. Hippocampal L-HATA volume in trauma-exposed individuals 83 European ancestry individuals, 74 African American or Afro-Caribbean individuals 79 African American or Afro-Caribbean post-traumatic stress disorder cases, 54 African American or Afro-Caribbean trauma-exposed controls Illumina [2711511] (imputed) 0 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST90239834 Genome-wide genotyping array 2022-12-02 33029326 Morey RA 2020-07-29 Eur J Psychotraumatol www.ncbi.nlm.nih.gov/pubmed/33029326 Genetic predictors of hippocampal subfield volume in PTSD cases and trauma-exposed controls. Hippocampal R-HATA volume in trauma-exposed individuals 83 European ancestry individuals, 74 African American or Afro-Caribbean individuals 79 African American or Afro-Caribbean post-traumatic stress disorder cases, 54 African American or Afro-Caribbean trauma-exposed controls Illumina [2711511] (imputed) 0 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST90239835 Genome-wide genotyping array 2022-04-11 34924555 Fontanillas P 2021-12-17 Pain www.ncbi.nlm.nih.gov/pubmed/34924555 Genome-wide association study of pain sensitivity assessed by questionnaire and the cold pressor test. Pain sensitivity measurement (Pain Sensitivity Questionnaire) 25,321 European ancestry individuals NA Illumina [13700000] (imputed) 3 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90101738 Genome-wide genotyping array 2022-04-11 34924555 Fontanillas P 2021-12-17 Pain www.ncbi.nlm.nih.gov/pubmed/34924555 Genome-wide association study of pain sensitivity assessed by questionnaire and the cold pressor test. Pain sensitivity measurement (Cold pressor test) 6,853 European ancestry individuals NA Illumina [13700000] (imputed) 1 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90101739 Genome-wide genotyping array 2022-05-11 35115687 Hautakangas H 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115687 Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles. Migraine 102,084 European ancestry cases, 771,257 European ancestry controls NA Illumina [10843197] (imputed) 123 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90102553 Genome-wide genotyping array 2022-07-08 35653334 Raghavan S 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653334 A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. Height 235,398 non-Hispanic white ancestry individuals, 63,898 non-Hispanic black ancestry individuals, 24,497 Hispanic American ancestry individuals NA Affymetrix [NR] (imputed) 29 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90105052 Genome-wide genotyping array 2022-07-08 35653334 Raghavan S 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653334 A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. Height 235,398 non-Hispanic white ancestry individuals NA Affymetrix [NR] (imputed) 22 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90105049 Genome-wide genotyping array 2022-07-08 35653334 Raghavan S 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653334 A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. Height 63,898 non-Hispanic black ancestry individuals NA Affymetrix [NR] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90105050 Genome-wide genotyping array 2022-07-08 35653334 Raghavan S 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653334 A multi-population phenome-wide association study of genetically-predicted height in the Million Veteran Program. Height 24,497 Hispanic American ancestry individuals NA Affymetrix [NR] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90105051 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine diacyl C42:1 levels 16,570 Caucasian ancestry individuals NA Affymetrix, Illumina [5791842] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010817 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Acetylcarnitine levels 31,008 Caucasian ancestry individuals NA Affymetrix, Illumina [6046365] (imputed) 4 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010754 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Acetylornithine levels 30,692 Caucasian ancestry individuals NA Affymetrix, Illumina [6046508] (imputed) 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90010743 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Alanine levels 86,413 Caucasian ancestry individuals NA Affymetrix, Illumina [6052021] (imputed) 20 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90010722 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. alpha-Aminoadipic acid levels 14,414 Caucasian ancestry individuals NA Affymetrix, Illumina [6077382] (imputed) 2 aminoadipic acid measurement http://www.ebi.ac.uk/efo/EFO_0010459 GCST90010745 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Arginine levels 30,724 Caucasian ancestry individuals NA Affymetrix, Illumina [6046728] (imputed) 10 L-arginine measurement http://www.ebi.ac.uk/efo/EFO_0006524 GCST90010723 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Asparagine levels 30,922 Caucasian ancestry individuals NA Affymetrix, Illumina [6046450] (imputed) 5 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90010724 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Aspartate levels 30,775 Caucasian ancestry individuals NA Affymetrix, Illumina [6046296] (imputed) 3 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90010725 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Butyrylcarnitine levels 30,694 Caucasian ancestry individuals NA Affymetrix, Illumina [6046389] (imputed) 6 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010756 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Carnitine levels 31,001 Caucasian ancestry individuals NA Affymetrix, Illumina [6046392] (imputed) 9 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010753 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Citrulline levels 30,940 Caucasian ancestry individuals NA Affymetrix, Illumina [6046410] (imputed) 6 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90010726 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Creatinine levels 84,794 Caucasian ancestry individuals NA Affymetrix, Illumina [6050906] (imputed) 19 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90010746 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Decanoylcarnitine levels 31,934 Caucasian ancestry individuals NA Affymetrix, Illumina [6043651] (imputed) 4 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010763 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Decenoylcarnitine levels 15,116 Caucasian ancestry individuals NA Affymetrix, Illumina [6083730] (imputed) 4 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010764 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Dodecanoylcarnitine levels 28,569 Caucasian ancestry individuals NA Affymetrix, Illumina [6042902] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010765 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Dodecenoylcarnitine levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791491] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010766 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Glutamate levels 30,977 Caucasian ancestry individuals NA Affymetrix, Illumina [6046372] (imputed) 1 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90010728 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Glutamine levels 85,821 Caucasian ancestry individuals NA Affymetrix, Illumina [6051950] (imputed) 13 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90010727 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Glycine levels 80,003 Caucasian ancestry individuals NA Affymetrix, Illumina [6053131] (imputed) 15 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90010729 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hexadecanoylcarnitine levels 30,915 Caucasian ancestry individuals NA Affymetrix, Illumina [6046326] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010770 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hexadecenoylcarnitine levels 14,370 Caucasian ancestry individuals NA Affymetrix, Illumina [6077273] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010771 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hexanoylcarnitine levels 9,363 Caucasian ancestry individuals NA Affymetrix, Illumina [6083013] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010759 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hexose levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5791391] (imputed) 2 hexose measurement http://www.ebi.ac.uk/efo/EFO_0007631 GCST90010862 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Histidine levels 80,809 Caucasian ancestry individuals NA Affymetrix, Illumina [6053918] (imputed) 9 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90010730 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Isoleucine levels 86,404 Caucasian ancestry individuals NA Affymetrix, Illumina [6052093] (imputed) 5 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90010731 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine 33:1 measurement http://www.ebi.ac.uk/efo/EFO_0021469 GCST90024284 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine 33:2 measurement http://www.ebi.ac.uk/efo/EFO_0021470 GCST90024285 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (34:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine 34:5 measurement http://www.ebi.ac.uk/efo/EFO_0021471 GCST90024286 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (35:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylcholine 35:5 measurement http://www.ebi.ac.uk/efo/EFO_0021472 GCST90024287 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (36:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine 36:0 measurement http://www.ebi.ac.uk/efo/EFO_0021473 GCST90024288 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (36:6) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine 36:6 measurement http://www.ebi.ac.uk/efo/EFO_0021474 GCST90024289 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 phosphatidylcholine 38:2 measurement http://www.ebi.ac.uk/efo/EFO_0010384 GCST90024290 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:4) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0010386 GCST90024291 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylcholine 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0010387 GCST90024292 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 19 phosphatidylcholine 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0010387 GCST90024293 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:6) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylcholine 38:6 measurement http://www.ebi.ac.uk/efo/EFO_0010388 GCST90024294 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:7) (c) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine 38:7 measurement http://www.ebi.ac.uk/efo/EFO_0021475 GCST90024295 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (39:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine 39:5 measurement http://www.ebi.ac.uk/efo/EFO_0021476 GCST90024296 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (39:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine 39:5 measurement http://www.ebi.ac.uk/efo/EFO_0021476 GCST90024297 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (40:7) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 phosphatidylcholine 40:7 measurement http://www.ebi.ac.uk/efo/EFO_0021477 GCST90024298 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (40:8) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine 40:8 measurement http://www.ebi.ac.uk/efo/EFO_0021478 GCST90024299 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024300 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024301 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024302 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024303 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024304 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024305 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024306 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024307 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:1/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024308 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-17:0/20:4) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024334 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024335 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024336 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/22:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024337 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024338 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:1/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024339 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:1/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024340 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-20:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024341 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-36:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024342 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-38:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024343 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-38:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024344 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024345 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 15 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024346 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024347 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024348 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024349 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_16:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024350 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024351 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024352 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024353 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024354 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 16 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024355 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024356 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024357 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024358 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:1_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024359 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:1_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024360 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024361 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024362 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024363 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024364 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024365 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 16 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024366 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 15 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024367 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024368 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024369 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024370 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:5) (n3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024371 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:5) (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024372 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024373 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024374 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 15 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024375 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_22:6) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024376 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_22:6) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024377 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (36:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024378 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (38:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024379 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (38:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024380 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024381 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024382 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024383 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024384 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024385 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024386 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/22:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024387 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024388 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:1/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024389 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:1/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024390 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-34:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024391 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-36:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024392 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-38:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024393 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-38:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024394 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024395 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/22:6) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024396 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/22:6) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024397 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024398 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024399 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024400 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 19 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024401 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024402 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024403 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024404 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024405 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:5) (n3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024406 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:5) (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024407 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024408 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:1/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024309 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-32:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024310 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-32:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024311 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024312 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024313 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024314 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-36:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024315 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-36:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024316 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-38:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024317 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024318 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:7) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024319 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:7) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024320 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-15:0/20:4) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024321 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-15:0/20:4) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024322 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024323 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024324 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/16:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024325 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024326 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024327 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024328 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024329 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024330 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024331 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024332 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-17:0/20:4) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024333 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024086 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024087 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024088 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024089 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024090 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024091 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024092 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 20 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024093 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:2_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024094 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:2_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024095 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM1 ganglioside (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 GM1 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021450 GCST90024096 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024097 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024098 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024099 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024100 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024101 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024102 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:2/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024103 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d16:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024104 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d16:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024105 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024106 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024107 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024108 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024109 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024110 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 20 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024061 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 18 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024062 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 16 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024063 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/26:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024064 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024065 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024066 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 16 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024067 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/26:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024068 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Free cholesterol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90024069 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024070 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024071 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024072 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024073 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024074 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024075 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (14:0_16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024076 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (14:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024077 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024078 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_16:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024079 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024080 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024081 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024082 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_22:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024083 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024084 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:1_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024085 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 lysophosphatidylcholine 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0020941 GCST90024136 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 lysophosphatidylcholine 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0020941 GCST90024137 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn1] [104_sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90024138 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn1] levels /Lysophosphatidylcholine (17:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90024139 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90024140 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90024141 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90024142 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:1) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90024143 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:1) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90024144 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021452 GCST90024145 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) (a) [sn1] [104_sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024146 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn1] (a) levels/ Lysophosphatidylcholine (17:1) [sn2] (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024147 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn1] (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024148 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn2] (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024149 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90024150 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90024151 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:1) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90024152 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:1) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90024153 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:2) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90024154 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:2) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90024155 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn1] (a) levels/Lysophosphatidylcholine (18:3) [sn2] (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90024156 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn1] levels (b) 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90024157 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn2] levels (a) 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90024158 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) (a) [sn1] [104_sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024159 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn1] (a) levels / Lysophosphatidylcholine (19:0) [sn2] (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024160 Genome-wide genotyping array 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (femoral neck) 2,948 African American individuals, 39,107 European ancestry individuals, 2,451 Hispanic individuals NA NR [15500000] (imputed) 32 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90101815 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (spine) 2,948 African American individuals, 39,107 European ancestry individuals, 2,451 Hispanic individuals NA NR [15500000] (imputed) 35 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90101816 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (femoral neck) 1,825 African American females, 26,724 European ancestry females, 1,683 Hispanic females NA NR [NR] (imputed) 15 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90101817 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (spine) 1,825 African American females, 26,724 European ancestry females, 1,683 Hispanic females NA NR [NR] (imputed) 27 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90101818 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (femoral neck) 1,123 African American males, 12,382 European ancestry males, 768 Hispanic males NA NR [NR] (imputed) 7 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90101819 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (spine) 1,123 African American males, 12,382 European ancestry males, 768 Hispanic males NA NR [NR] (imputed) 6 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90101820 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (femoral neck) 2,948 African American individuals NA NR [NR] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90101821 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (spine) 2,948 African American individuals NA NR [NR] (imputed) 0 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90101822 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (femoral neck) 2,451 Hispanic individuals NA NR [NR] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90101823 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-04-13 34673960 Greenbaum J 2021-10-21 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34673960 A multi-ethnic whole genome sequencing study to identify novel loci for bone mineral density. Bone mineral density (spine) 2,451 Hispanic individuals NA NR [NR] (imputed) 0 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90101824 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-07-22 35455731 Chen CK 2022-04-11 J Pers Med www.ncbi.nlm.nih.gov/pubmed/35455731 Antidepressant Treatment and Manic Switch in Bipolar I Disorder: A Clinical and Molecular Genetic Study. Manic switch in bipolar I disorder with depressive episode 353 Taiwanese Han ancestry switch cases, 393 Taiwanese Han ancestry no switch cases 106 Taiwanese Han ancestry switch cases, 149 Taiwanese Han ancestry no switch cases Illumina [4750978] (imputed) 1 manic or hypomanic episode http://www.ebi.ac.uk/efo/EFO_0007706 GCST90129606 Genome-wide genotyping array 2022-08-04 35710981 Liu H 2022-06-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35710981 Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease. Estimated glomerular filtration rate (creatinine) 1,205,871 European ancestry individuals, 168,300 East Asian ancestry individuals, 63,553 African ancestry individuals, 23,509 Hispanic or Latin American individuals, 22,103 African American individuals, 21,791 Central Asian or South Asian ancestry individuals, 1,502 Middle Eastern ancestry individuals, 939 other admixed ancestry individuals, 602 Native American ancestry individuals, 150 Asian ancestry individuals, 339 individuals NA Affymetrix, Illumina [12653804] (imputed) 878 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90100220 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024111 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:2/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024112 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:2/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024113 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024114 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024115 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024116 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024117 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024118 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024119 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024120 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024121 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024122 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024123 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024124 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024125 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 15 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024126 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024127 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 19 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024128 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024129 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024130 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024131 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024132 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024133 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (14:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90024134 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (14:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90024135 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:1) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90024211 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:2) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90024212 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:2) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90024213 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (20:4) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90024214 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (20:4) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90024215 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (22:6) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90024216 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (22:6) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90024217 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024218 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024219 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024220 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024221 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024222 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024223 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:1) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024224 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:1) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024225 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:2) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024226 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:2) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024227 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (20:4) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024228 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (20:4) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024229 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Oxidized cholesteryl ester (18:2) [+2O] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024230 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Oxidized cholesteryl ester (18:2) [+O] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024231 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024232 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024233 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024234 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024235 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn1] levels (b) 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024161 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn2] levels (a) 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024162 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 lysophosphatidylcholine 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021456 GCST90024163 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021456 GCST90024164 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:1) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90024165 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:1) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90024166 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:2) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 lysophosphatidylcholine 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021458 GCST90024167 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:2) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 lysophosphatidylcholine 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021458 GCST90024168 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:3) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90024169 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:3) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90024170 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:4) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90024171 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:4) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90024172 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:5) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90024173 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:5) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90024174 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021459 GCST90024175 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021459 GCST90024176 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:1) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021460 GCST90024177 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:1) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021460 GCST90024178 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:4) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90024179 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:4) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90024180 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn1] (n3) levels/Lysophosphatidylcholine (22:5) [sn2] (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90024181 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn1] (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90024182 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn2] (n3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90024183 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:6) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90024184 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:6) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90024185 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (24:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90024186 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (24:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90024187 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (26:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 26:0 measurement http://www.ebi.ac.uk/efo/EFO_0021464 GCST90024188 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (26:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 lysophosphatidylcholine 26:0 measurement http://www.ebi.ac.uk/efo/EFO_0021464 GCST90024189 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024190 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024191 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024192 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024193 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-20:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024194 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024195 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-22:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024196 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024197 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024198 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024199 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024200 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024201 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024202 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024203 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (16:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90024204 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (16:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90024205 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (17:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 lysophosphatidylethanolamine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021465 GCST90024206 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (17:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 lysophosphatidylethanolamine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021465 GCST90024207 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:0) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90024208 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:0) [sn2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90024209 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:1) [sn1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90024210 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-52:2) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024575 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Acylcarnitine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024576 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Cholesteryl ester levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024577 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Ceramide levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024578 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total free cholesterol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90024579 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dehydrocholesteryl ester levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024580 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Diacylglycerol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024581 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dihexosylceramide levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024582 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dihydroceramide levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024583 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total GM1 ganglioside levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 GM1 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021450 GCST90024584 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total GM3 ganglioside levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024585 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylcholine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024586 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkylphosphatidylcholine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024587 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkenylphosphatidylcholine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024588 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylethanolamine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024589 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkenylphosphatidylethanolamine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024590 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylinositol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024591 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Monohexosylceramide levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024592 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Oxidized sterol ester levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90024593 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylcholine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024594 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkylphosphatidylcholine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024595 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkenylphosphatidylcholine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024596 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylethanolamine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024597 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkylphosphatidylethanolamine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024598 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkenylphosphatidylethanolamine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024599 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:0) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 51:0 measurement http://www.ebi.ac.uk/efo/EFO_0021481 GCST90024550 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:1) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90024551 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-15:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90024552 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90024553 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90024554 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:1) [NL-18:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 52:1 measurement http://www.ebi.ac.uk/efo/EFO_0010413 GCST90024555 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:2) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90024556 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:3) [NL-16:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90024557 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:3) [NL-18:2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90024558 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:4) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90024559 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:4) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90024560 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (53:2) [NL-17:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90024561 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:0) [NL-18:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 54:0 measurement http://www.ebi.ac.uk/efo/EFO_0021485 GCST90024562 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:1) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 triacylglycerol 54:1 measurement http://www.ebi.ac.uk/efo/EFO_0010419 GCST90024563 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:2) [NL-18:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 triacylglycerol 54:2 measurement http://www.ebi.ac.uk/efo/EFO_0010420 GCST90024564 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:3) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90024565 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:4) [NL-18:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90024566 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:4) [NL-18:2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90024567 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:5) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90024568 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:6) [NL-18:2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90024569 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (56:6) [NL-20:4] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90024570 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (56:8) [NL-20:4] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90024571 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (58:8) [NL-22:6] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90024572 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-50:1) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024573 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-52:0) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024574 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylglycerol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90024600 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylinositol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024601 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylserine levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90024602 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Sphingomyelin levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024603 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Sulfatide levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024604 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Triacylglycerol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90024605 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkyldiacylglycerol levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024606 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Trihexosylcermide levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024607 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Ubiquinone levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90024608 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ubiquinone levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90024609 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (12:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024610 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (13:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024611 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024612 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024613 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024614 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (15:0) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024615 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (15:0) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024616 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90024617 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:1/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025548 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-32:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025549 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-32:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025550 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025551 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025552 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025553 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-36:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025554 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Kynurenine levels 30,899 Caucasian ancestry individuals NA Affymetrix, Illumina [6046416] (imputed) 4 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90010747 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Leucine levels 86,351 Caucasian ancestry individuals NA Affymetrix, Illumina [6052280] (imputed) 6 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90010732 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Lysine levels 30,982 Caucasian ancestry individuals NA Affymetrix, Illumina [6046356] (imputed) 9 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90010733 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C14:0 levels 9,363 Caucasian ancestry individuals NA Affymetrix, Illumina [6083623] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010775 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C16:0 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792440] (imputed) 3 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010782 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C16:1 levels 16,836 Caucasian ancestry individuals NA Affymetrix, Illumina [5791495] (imputed) 3 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010776 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C17:0 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791690] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010777 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C18:0 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792004] (imputed) 5 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010778 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C18:1 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791467] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010783 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C18:2 levels 16,837 Caucasian ancestry individuals NA Affymetrix, Illumina [5791071] (imputed) 2 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010779 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C20:3 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792163] (imputed) 5 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010784 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C20:4 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791771] (imputed) 4 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010780 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C24:0 levels 9,363 Caucasian ancestry individuals NA Affymetrix, Illumina [6083871] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010785 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C26:0 levels 9,363 Caucasian ancestry individuals NA Affymetrix, Illumina [6083737] (imputed) 2 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010786 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C26:1 levels 9,363 Caucasian ancestry individuals NA Affymetrix, Illumina [6083819] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010781 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C28:0 levels 15,963 Caucasian ancestry individuals NA Affymetrix, Illumina [6084421] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010787 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. lysoPhosphatidylcholine acyl C28:0 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5792091] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90010788 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Methionine levels 30,967 Caucasian ancestry individuals NA Affymetrix, Illumina [6046489] (imputed) 1 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90010734 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Methioninesulfoxide levels 23,469 Caucasian ancestry individuals NA Affymetrix, Illumina [6093711] (imputed) 1 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90010748 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Methylglutarylcarnitine levels 22,335 Caucasian ancestry individuals NA Affymetrix, Illumina [6093101] (imputed) 6 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010758 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Nonaylcarnitine levels 13,925 Caucasian ancestry individuals NA Affymetrix, Illumina [6083678] (imputed) 2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010762 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Octadecandienylcarnitine levels 31,129 Caucasian ancestry individuals NA Affymetrix, Illumina [6058871] (imputed) 4 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010774 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Octadecanoylcarnitine levels 30,138 Caucasian ancestry individuals NA Affymetrix, Illumina [6039747] (imputed) 6 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010772 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Octadecenoylcarnitine levels 15,967 Caucasian ancestry individuals NA Affymetrix, Illumina [6084364] (imputed) 2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010773 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Octanoylcarnitine levels 31,969 Caucasian ancestry individuals NA Affymetrix, Illumina [6043492] (imputed) 5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010761 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024259 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:1_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024260 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024261 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024262 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024263 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 29 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024264 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024265 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:5) (n3) levels/Phosphatidylcholine (20:1_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024266 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:5) (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024267 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024268 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024269 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024270 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024271 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_22:6) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024272 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_22:6) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024273 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:2_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024274 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:2_20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024275 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (20:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024276 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (28:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine 28:0 measurement http://www.ebi.ac.uk/efo/EFO_0021466 GCST90024277 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (31:0) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine 31:0 measurement http://www.ebi.ac.uk/efo/EFO_0021467 GCST90024278 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (31:0) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine 31:0 measurement http://www.ebi.ac.uk/efo/EFO_0021467 GCST90024279 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (32:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine 32:1 measurement http://www.ebi.ac.uk/efo/EFO_0010373 GCST90024280 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (32:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90024281 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:0) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine 33:0 measurement http://www.ebi.ac.uk/efo/EFO_0021468 GCST90024282 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:0) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine 33:0 measurement http://www.ebi.ac.uk/efo/EFO_0021468 GCST90024283 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C40:1 levels 16,765 Caucasian ancestry individuals NA Affymetrix, Illumina [5792181] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010839 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C40:3 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5793024] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010840 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C40:4 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792704] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010841 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C40:5 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792541] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010842 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C40:6 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791707] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010843 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C42:1 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5792614] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010844 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C42:2 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5792187] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010845 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C42:3 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791892] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010846 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C42:4 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792022] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010847 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C42:5 levels 15,967 Caucasian ancestry individuals NA Affymetrix, Illumina [6084572] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010848 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C44:5 levels 16,685 Caucasian ancestry individuals NA Affymetrix, Illumina [5791751] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010849 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phosphatidylcholine acyl-alkyl C44:6 levels 16,564 Caucasian ancestry individuals NA Affymetrix, Illumina [5791983] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90010850 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Phenylalanine levels 84,297 Caucasian ancestry individuals NA Affymetrix, Illumina [6055439] (imputed) 8 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90010736 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Pimelylcarnitine levels 15,119 Caucasian ancestry individuals NA Affymetrix, Illumina [6083180] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010760 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Proline levels 30,985 Caucasian ancestry individuals NA Affymetrix, Illumina [6046366] (imputed) 3 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90010737 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Propionylcarnitine levels 32,590 Caucasian ancestry individuals NA Affymetrix, Illumina [6045556] (imputed) 6 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010755 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sarcosine levels 22,912 Caucasian ancestry individuals NA Affymetrix, Illumina [6093787] (imputed) 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90010750 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Serine levels 30,955 Caucasian ancestry individuals NA Affymetrix, Illumina [6046388] (imputed) 5 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90010738 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hydroxysphingomyeline C14:1 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791165] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010858 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hydroxysphingomyeline C16:1 levels 15,899 Caucasian ancestry individuals NA Affymetrix, Illumina [6083887] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010859 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hydroxysphingomyeline C22:1 levels 15,899 Caucasian ancestry individuals NA Affymetrix, Illumina [6084448] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010860 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Hydroxysphingomyeline C22:2 levels 15,757 Caucasian ancestry individuals NA Affymetrix, Illumina [6084053] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010861 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sphingomyeline C16:0 levels 31,023 Caucasian ancestry individuals NA Affymetrix, Illumina [6046342] (imputed) 11 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010851 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sphingomyeline C16:1 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791919] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010852 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sphingomyeline C18:0 levels 31,120 Caucasian ancestry individuals NA Affymetrix, Illumina [6058838] (imputed) 12 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010853 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sphingomyeline C18:1 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5791473] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010854 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sphingomyeline C20:2 levels 16,762 Caucasian ancestry individuals NA Affymetrix, Illumina [5791217] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010855 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sphingomyeline C24:0 levels 16,838 Caucasian ancestry individuals NA Affymetrix, Illumina [5791726] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010856 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Sphingomyeline C24:1 levels 16,839 Caucasian ancestry individuals NA Affymetrix, Illumina [5792136] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90010857 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Spermidine levels 16,699 Caucasian ancestry individuals NA Affymetrix, Illumina [6090968] (imputed) 2 butyrylcholinesterase measurement http://www.ebi.ac.uk/efo/EFO_0004571 GCST90010751 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Symmetric dimethylarginine levels 9,256 Caucasian ancestry individuals NA Affymetrix, Illumina [6083518] (imputed) 1 symmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006523 GCST90010744 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Taurine levels 23,553 Caucasian ancestry individuals NA Affymetrix, Illumina [6093547] (imputed) 1 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90010752 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Tetradecadienylcarnitine levels 15,118 Caucasian ancestry individuals NA Affymetrix, Illumina [6083929] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010769 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Tetradecanoylcarnitine levels 23,445 Caucasian ancestry individuals NA Affymetrix, Illumina [6093394] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010767 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Tetradecenoylcarnitine levels 31,105 Caucasian ancestry individuals NA Affymetrix, Illumina [6058849] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010768 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Threonine levels 29,276 Caucasian ancestry individuals NA Affymetrix, Illumina [6042426] (imputed) 7 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90010739 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. trans-Hydroxyproline levels 30,895 Caucasian ancestry individuals NA Affymetrix, Illumina [6046415] (imputed) 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90010749 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Tryptophan levels 30,974 Caucasian ancestry individuals NA Affymetrix, Illumina [6046425] (imputed) 2 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90010740 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Tyrosine levels 86,507 Caucasian ancestry individuals NA Affymetrix, Illumina [6036766] (imputed) 8 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90010741 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Valerylcarnitine levels 9,363 Caucasian ancestry individuals NA Affymetrix, Illumina [6083606] (imputed) 4 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90010757 Genome-wide genotyping array 2022-05-10 33414548 Lotta LA 2021-01-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33414548 A cross-platform approach identifies genetic regulators of human metabolism and health. Valine levels 85,641 Caucasian ancestry individuals NA Affymetrix, Illumina [6051188] (imputed) 7 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90010742 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of omega-6 fatty acids to total fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 64 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092935 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phosphatidylcholine levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 69 phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092937 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phosphoglycerides levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 69 phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092938 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of polyunsaturated fatty acids to monounsaturated fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 74 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092940 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of polyunsaturated fatty acids to total fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 59 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092941 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Remnant cholesterol (non-HDL, non-LDL -cholesterol) 115,082 European ancestry individuals NA NR [11722792] (imputed) 64 remnant cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010815 GCST90092943 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 60 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092944 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 72 cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092945 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 61 cholesteryl ester measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092946 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 67 cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020944, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092947 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 59 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092948 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of medium HDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 86 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092899 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 85 free cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020945, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092949 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 56 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092950 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of small HDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 60 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092951 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 65 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092952 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in small HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 74 phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020946, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092953 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 98 triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092927 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Monounsaturated fatty acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 89 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092928 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of monounsaturated fatty acids to total fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 87 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092929 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total cholesterol minus HDL-C levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 63 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90092930 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Omega-3 fatty acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 61 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90092931 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of omega-3 fatty acids to total fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 49 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092932 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Omega-6 fatty acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 81 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90092933 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of omega-6 fatty acids to omega-3 fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 42 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092934 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_18:1) levels/Phosphatidylinositol (17:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024459 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_18:2) levels/Phosphatidylinositol (17:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024460 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024461 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024462 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024463 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024464 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024465 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024466 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:5) (n3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024467 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:5) (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024468 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024469 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:1_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024470 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (20:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024471 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (34:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024472 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (34:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024473 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (36:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024474 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (37:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024475 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:5) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024476 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:5) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024477 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024478 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (12:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023981 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (13:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023982 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023983 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023984 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023985 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (15:0) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023986 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (15:0) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023987 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023988 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (16:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023989 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (17:0) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023990 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (17:0) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023991 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023992 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023993 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90023994 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 cholesteryl ester 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010340 GCST90023995 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (15:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 cholesteryl ester 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021434 GCST90023996 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90023997 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90023998 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester 16:2 measurement http://www.ebi.ac.uk/efo/EFO_0021435 GCST90023999 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (17:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 cholesteryl ester 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021436 GCST90024000 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (17:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 cholesteryl ester 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021437 GCST90024001 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90024002 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90024003 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90024004 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90024005 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 cholesteryl ester 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021438 GCST90024006 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 cholesteryl ester 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021439 GCST90024007 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 cholesteryl ester 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021440 GCST90024008 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90024009 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 19 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90024010 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90024011 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 cholesteryl ester 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021441 GCST90024012 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021442 GCST90024013 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 cholesteryl ester 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021443 GCST90024014 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:5) (n3) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90024015 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:5) (n6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90024016 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90024017 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021445 GCST90024018 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 cholesteryl ester 24:1 measurement http://www.ebi.ac.uk/efo/EFO_0021446 GCST90024019 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 cholesteryl ester 24:4 measurement http://www.ebi.ac.uk/efo/EFO_0021447 GCST90024020 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 cholesteryl ester 24:5 measurement http://www.ebi.ac.uk/efo/EFO_0021448 GCST90024021 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 cholesteryl ester 24:6 measurement http://www.ebi.ac.uk/efo/EFO_0021449 GCST90024022 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024023 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024024 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 14 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024025 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024026 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024027 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024028 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024029 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024030 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024031 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024032 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024033 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024034 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024035 Genome-wide genotyping array 2022-04-11 34581777 Downes K 2021-09-28 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34581777 G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. Platelet reactivity in response to ADP 1,341 European ancestry individuals NA Affymetrix [NR] (imputed) 2 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST90101809 Genome-wide genotyping array 2022-04-11 34581777 Downes K 2021-09-28 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34581777 G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. Platelet reactivity in response to CRP-XL 1,329 European ancestry individuals NA Affymetrix [NR] (imputed) 1 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST90101810 Genome-wide genotyping array 2022-04-11 34581777 Downes K 2021-09-28 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34581777 G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. Platelet reactivity in response to PAR-1 550 European ancestry individuals NA Affymetrix [NR] (imputed) 1 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST90101811 Genome-wide genotyping array 2022-04-11 34581777 Downes K 2021-09-28 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34581777 G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. Platelet reactivity in response to PAR-4 550 European ancestry individuals NA Affymetrix [NR] (imputed) 2 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST90101812 Genome-wide genotyping array 2022-04-11 34581777 Downes K 2021-09-28 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34581777 G protein-coupled receptor kinase 5 regulates thrombin signaling in platelets via PAR-1. Platelet reactivity in response to TRAP-6 606 European ancestry individuals 253 individuals Affymetrix [NR] (imputed) 0 platelet reactivity measurement http://www.ebi.ac.uk/efo/EFO_0004985 GCST90101813 Genome-wide genotyping array 2022-05-05 35023183 Xia M 2022-01-12 Aliment Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35023183 NAFLD-related gene polymorphisms and all-cause and cause-specific mortality in an Asian population: the Shanghai Changfeng Study. Nonalcoholic fatty liver disease 4,645 Chinese ancestry individuals NA Illumina [707180] 1 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90102471 Genome-wide genotyping array 2022-05-05 35023183 Xia M 2022-01-12 Aliment Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35023183 NAFLD-related gene polymorphisms and all-cause and cause-specific mortality in an Asian population: the Shanghai Changfeng Study. Nonalcoholic fatty liver disease (without other liver diseases) 5,182 Chinese ancestry individuals NA Illumina [707180] 0 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90102472 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 17 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024236 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024237 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024238 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024239 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024240 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024241 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024242 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024243 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024244 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024245 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024246 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024247 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:3) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 9 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024248 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:3) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024249 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 24 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024250 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:5) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024251 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024252 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 11 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024253 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024254 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_22:6) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024255 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024256 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_18:2) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024257 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_20:4) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 20 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024258 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025292 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025293 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025294 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025295 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/26:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025296 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025297 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025298 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025299 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 6 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025300 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025301 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 7 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025302 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/26:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025303 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025304 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025305 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025306 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/26:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025307 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Free cholesterol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90025308 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025309 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025310 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025311 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025312 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025313 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025314 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (14:0_16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025315 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (14:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025316 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025317 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_16:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025318 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d16:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025344 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025345 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025346 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025347 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025348 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025349 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025350 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:2/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025351 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:2/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025352 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025353 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025354 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025355 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025356 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025357 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025358 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025359 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025360 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025361 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d16:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025362 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025363 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025364 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025365 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025366 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025367 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025368 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025319 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025320 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025321 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_22:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025322 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025323 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:1_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025324 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025325 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025326 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025327 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025328 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025329 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025330 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025331 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025332 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:2_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025333 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:2_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025334 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM1 ganglioside (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM1 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021450 GCST90025335 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025336 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025337 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025338 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025339 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025340 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025341 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:2/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025342 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d16:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025343 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025369 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025370 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025371 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:2/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025372 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (14:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90025373 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (14:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90025374 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0020941 GCST90025375 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0020941 GCST90025376 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn1] [104_sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90025377 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn1] levels /Lysophosphatidylcholine (17:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90025378 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90025379 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90025380 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90025381 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:1) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90025382 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:1) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90025383 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021452 GCST90025384 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) (a) [sn1] [104_sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90025385 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn1] (a) levels/ Lysophosphatidylcholine (17:1) [sn2] (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90025386 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn1] (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90025387 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn2] (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90025388 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:0) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90025389 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:0) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90025390 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:1) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90025391 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:1) [sn2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90025392 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:2) [sn1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90025393 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:0) [NL-18:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 50:0 measurement http://www.ebi.ac.uk/efo/EFO_0021480 GCST90024540 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:1) [NL-14:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90024541 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:1) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90024542 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90024543 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90024544 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025483 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025484 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025485 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025486 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025487 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025488 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 10 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025489 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025490 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025491 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025492 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025493 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025494 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025495 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025496 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 7 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025497 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025498 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:1_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025499 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025500 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025501 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025502 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/17:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024515 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024516 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/18:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024517 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 6 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024518 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024519 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/23:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024520 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024521 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d19:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 12 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024522 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 13 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024523 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/16:0(OH) levels) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024524 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024525 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:0(OH) levels) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024526 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024527 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:1(OH) levels) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024528 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:0) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90024529 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:1) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90024530 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-14:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90024531 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90024532 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-16:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90024533 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90024534 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:3) [NL-16:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90024535 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:3) [NL-18:2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90024536 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-15:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90024537 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-16:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90024538 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90024539 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (36:6) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 36:6 measurement http://www.ebi.ac.uk/efo/EFO_0021474 GCST90025528 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine 38:2 measurement http://www.ebi.ac.uk/efo/EFO_0010384 GCST90025529 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:4) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0010386 GCST90025530 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylcholine 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0010387 GCST90025531 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0010387 GCST90025532 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:6) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine 38:6 measurement http://www.ebi.ac.uk/efo/EFO_0010388 GCST90025533 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:7) (c) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 38:7 measurement http://www.ebi.ac.uk/efo/EFO_0021475 GCST90025534 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (39:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 39:5 measurement http://www.ebi.ac.uk/efo/EFO_0021476 GCST90025535 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (39:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine 39:5 measurement http://www.ebi.ac.uk/efo/EFO_0021476 GCST90025536 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (40:7) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 40:7 measurement http://www.ebi.ac.uk/efo/EFO_0021477 GCST90025537 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (40:8) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine 40:8 measurement http://www.ebi.ac.uk/efo/EFO_0021478 GCST90025538 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025539 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025540 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025541 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025542 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025543 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025544 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025545 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025546 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:1/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025547 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:2] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90024545 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-14:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90024546 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-16:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90024547 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-18:1] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90024548 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:4) [NL-14:0] levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90024549 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (41:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024490 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (41:1) (a) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 10 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024491 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024492 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:2) (b) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024493 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:2) (c) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024494 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/19:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024495 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/23:0) levels/Sphingomyelin (d17:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024496 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024497 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024498 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024499 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024500 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024501 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024502 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024503 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/14:0) levels/Sphingomyelin (d16:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 8 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024504 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024505 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/17:0) levels/Sphingomyelin (d17:1/18:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024506 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/18:0) levels/Sphingomyelin (d16:1/20:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024507 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/20:0) levels/Sphingomyelin (d16:1/22:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 7 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024508 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/22:0) levels/Sphingomyelin (d16:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024509 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/23:0) levels/Sphingomyelin (d17:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024510 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/24:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024511 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/24:1) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024512 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/14:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024513 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/16:0) levels 4,492 European ancestry individuals NA Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90024514 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 10 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025503 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025504 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:5) (n3) levels/Phosphatidylcholine (20:1_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025505 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:5) (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025506 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025507 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025508 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025509 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025510 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_22:6) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025511 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_22:6) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025512 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:2_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025513 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:2_20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025514 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (20:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025515 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (28:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 28:0 measurement http://www.ebi.ac.uk/efo/EFO_0021466 GCST90025516 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (31:0) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 31:0 measurement http://www.ebi.ac.uk/efo/EFO_0021467 GCST90025517 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (31:0) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 31:0 measurement http://www.ebi.ac.uk/efo/EFO_0021467 GCST90025518 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (32:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 32:1 measurement http://www.ebi.ac.uk/efo/EFO_0010373 GCST90025519 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (32:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90025520 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:0) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 33:0 measurement http://www.ebi.ac.uk/efo/EFO_0021468 GCST90025521 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:0) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 33:0 measurement http://www.ebi.ac.uk/efo/EFO_0021468 GCST90025522 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 33:1 measurement http://www.ebi.ac.uk/efo/EFO_0021469 GCST90025523 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 33:2 measurement http://www.ebi.ac.uk/efo/EFO_0021470 GCST90025524 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (34:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine 34:5 measurement http://www.ebi.ac.uk/efo/EFO_0021471 GCST90025525 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (35:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine 35:5 measurement http://www.ebi.ac.uk/efo/EFO_0021472 GCST90025526 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (36:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine 36:0 measurement http://www.ebi.ac.uk/efo/EFO_0021473 GCST90025527 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025685 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:1/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025686 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:1/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025687 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (34:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025688 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (34:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025689 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (36:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025690 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (36:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025691 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_20:4) levels/Phosphatidylinositol (17:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025692 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025693 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_16:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025694 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025695 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025696 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025697 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_18:1) levels/Phosphatidylinositol (17:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025698 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_18:2) levels/Phosphatidylinositol (17:0_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025699 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025700 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025701 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025702 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025703 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025704 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025705 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:5) (n3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025706 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:5) (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025707 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025708 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:1_18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025709 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024721 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:2_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024722 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:2_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024723 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM1 ganglioside (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 GM1 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021450 GCST90024724 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024725 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024726 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024727 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024728 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024729 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. GM3 ganglioside (d18:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90024730 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024731 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024732 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024733 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024734 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024735 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihexosylceramide (d18:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024736 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024737 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025677 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:6) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025678 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:6) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025679 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-19:0/20:4) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025680 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-19:0/20:4) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025681 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025682 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025683 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025684 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90024757 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:1) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90024758 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:1) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90024759 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 lysophosphatidylcholine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021452 GCST90024760 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) (a) [sn1] [104_sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024761 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn1] (a) levels/ Lysophosphatidylcholine (17:1) [sn2] (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024762 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn1] (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024763 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (17:1) [sn2] (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021453 GCST90024764 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90024765 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90024766 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:1) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90024767 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:1) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90024768 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:2) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90024769 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:2) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90024770 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn1] (a) levels/Lysophosphatidylcholine (18:3) [sn2] (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90024771 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn1] levels (b) 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90024772 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (18:3) [sn2] levels (a) 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90024773 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) (a) [sn1] [104_sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024774 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn1] (a) levels / Lysophosphatidylcholine (19:0) [sn2] (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024775 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn1] levels (b) 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024776 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (19:0) [sn2] levels (a) 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021455 GCST90024777 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021456 GCST90024778 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021456 GCST90024779 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:1) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90024780 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:1) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90024781 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (20:0_20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025710 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (34:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025711 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (34:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025712 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (36:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025713 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (37:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025714 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025715 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025716 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025717 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (39:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025718 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (36:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025719 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (36:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025720 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025721 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025722 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025723 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (40:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025724 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (40:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025725 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (34:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025726 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (35:2) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025727 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (37:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025728 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (41:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025729 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (41:1) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025730 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025731 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:2) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025732 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:2) (c) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025733 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/19:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025734 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025670 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:4) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025671 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:4) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025672 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025673 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025674 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025675 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025676 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024678 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/17:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024679 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024680 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024681 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024682 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024683 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024684 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/26:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024685 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024686 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024687 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024688 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024689 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024690 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 9 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024691 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d19:1/26:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024692 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024693 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024694 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024695 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d20:1/26:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024696 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Free cholesterol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90024697 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024698 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024699 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024700 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024701 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (20:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024702 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dehydrocholesteryl ester (22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90024703 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (14:0_16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024704 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (14:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024705 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024706 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_16:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024707 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024708 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024709 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024710 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_22:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024711 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024712 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (16:1_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024713 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024714 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024715 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024716 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024717 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024718 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_18:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024719 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Diacylglycerol (18:1_20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90024720 Genome-wide genotyping array 2022-02-15 34424336 Mobuchon L 2021-08-23 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/34424336 Different Pigmentation Risk Loci for High-Risk Monosomy 3 and Low-Risk Disomy 3 Uveal Melanomas. Uveal melanoma 1,142 European ancestry cases, 882 European ancestry controls NA Illumina [7488175] (imputed) 12 Uveal Melanoma http://www.ebi.ac.uk/efo/EFO_1000616 GCST90094626 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. B-cell receptor CD22 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 B-cell receptor CD22 measurement http://www.ebi.ac.uk/efo/EFO_0020171 GCST90100686 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bactericidal permeability-increasing protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bactericidal permeability-increasing protein measurement http://www.ebi.ac.uk/efo/EFO_0020172 GCST90100687 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Baculoviral IAP repeat-containing protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 baculoviral IAP repeat-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020173 GCST90100688 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Baculoviral IAP repeat-containing protein 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 baculoviral IAP repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020174 GCST90100689 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Baculoviral IAP repeat-containing protein 7 Isoform beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 baculoviral IAP repeat-containing protein 7 isoform beta measurement http://www.ebi.ac.uk/efo/EFO_0020175 GCST90100690 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bcl-2-related protein A1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 BCL-2-related protein A1 measurement http://www.ebi.ac.uk/efo/EFO_0020178 GCST90100694 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Beta-2-microglobulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 beta-2-microglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020180 GCST90100696 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. beta-adrenergic receptor kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 beta-adrenergic receptor kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020181 GCST90100697 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Beta-Ala-His dipeptidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 beta-Ala-His dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0008033 GCST90100698 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Beta-endorphin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90100699 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. beta-nerve growth factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST90100700 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bone morphogenetic protein receptor type-1A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bone morphogenetic protein receptor type-1a measurement http://www.ebi.ac.uk/efo/EFO_0020188 GCST90100707 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bone morphogenetic protein receptor type-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bone morphogenetic protein receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020189 GCST90100708 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bone sialoprotein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bone sialoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020190 GCST90100709 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Brain natriuretic peptide 32 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 brain natriuretic peptide 32 measurement http://www.ebi.ac.uk/efo/EFO_0020191 GCST90100710 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Brain-derived neurotrophic factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST90100711 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Brain-specific serine protease 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 brain-specific serine protease 4 measurement http://www.ebi.ac.uk/efo/EFO_0020192 GCST90100712 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Breast cancer anti-estrogen resistance protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 breast cancer anti-estrogen resistance protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008040 GCST90100713 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Brevican core protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 brevican core protein measurement http://www.ebi.ac.uk/efo/EFO_0020193 GCST90100714 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Brother of CDO levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 brother of CDO measurement http://www.ebi.ac.uk/efo/EFO_0020194 GCST90100715 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-C motif chemokine 1 measurement http://www.ebi.ac.uk/efo/EFO_0008041 GCST90100716 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 13 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020195 GCST90100717 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 C-C motif chemokine 14 measurement http://www.ebi.ac.uk/efo/EFO_0008042 GCST90100718 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 15 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90100719 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 16 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90100720 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 17 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 C-C motif chemokine 17 measurement http://www.ebi.ac.uk/efo/EFO_0008045 GCST90100721 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 18 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 C-C motif chemokine 18 measurement http://www.ebi.ac.uk/efo/EFO_0008046 GCST90100722 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 19 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-C motif chemokine 19 measurement http://www.ebi.ac.uk/efo/EFO_0008047 GCST90100723 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90100724 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 20 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-C motif chemokine 20 measurement http://www.ebi.ac.uk/efo/EFO_0010910 GCST90100725 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 21 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-C motif chemokine 21 measurement http://www.ebi.ac.uk/efo/EFO_0008048 GCST90100726 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase receptor TYRO3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase receptor TYRO3 measurement http://www.ebi.ac.uk/efo/EFO_0020829 GCST90101677 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Tec levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase TEC measurement http://www.ebi.ac.uk/efo/EFO_0020830 GCST90101678 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase transmembrane receptor ROR1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase transmembrane receptor ROR1 measurement http://www.ebi.ac.uk/efo/EFO_0020831 GCST90101679 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Yes levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase YES measurement http://www.ebi.ac.uk/efo/EFO_0020832 GCST90101680 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase ZAP-70 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase ZAP-70 measurement http://www.ebi.ac.uk/efo/EFO_0020833 GCST90101681 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Atrial natriuretic factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 atrial natriuretic factor measurement http://www.ebi.ac.uk/efo/EFO_0004789 GCST90100682 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Aurora kinase A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 aurora kinase A measurement http://www.ebi.ac.uk/efo/EFO_0020168 GCST90100683 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Aurora kinase B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 aurora kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020169 GCST90100684 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Azurocidin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 azurocidin measurement http://www.ebi.ac.uk/efo/EFO_0020170 GCST90100685 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Basal Cell Adhesion Molecule levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 basal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008032 GCST90100691 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Basigin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 basigin measurement http://www.ebi.ac.uk/efo/EFO_0020176 GCST90100692 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bcl-2-like protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 BCL-2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020177 GCST90100693 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. BDNF/NT-3 growth factors receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bdnf/nt-3 growth factors receptor measurement http://www.ebi.ac.uk/efo/EFO_0020179 GCST90100695 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Biglycan levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 biglycan measurement http://www.ebi.ac.uk/efo/EFO_0020182 GCST90100701 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. BMP-binding endothelial regulator protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 BMP-binding endothelial regulator protein measurement http://www.ebi.ac.uk/efo/EFO_0020183 GCST90100702 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bone morphogenetic protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bone morphogenetic protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020184 GCST90100703 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bone morphogenetic protein 10 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bone morphogenetic protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020185 GCST90100704 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bone morphogenetic protein 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90100705 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Bone morphogenetic protein 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 bone morphogenetic protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020187 GCST90100706 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein phosphatase non-receptor type 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90101682 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein phosphatase non-receptor type 11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90101683 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein phosphatase non-receptor type 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein phosphatase non-receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0020836 GCST90101684 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein phosphatase non-receptor type 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein phosphatase non-receptor type 6 measurement http://www.ebi.ac.uk/efo/EFO_0020837 GCST90101685 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ubiquitin carboxyl-terminal hydrolase isozyme L1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ubiquitin carboxyl-terminal hydrolase isozyme L1 measurement http://www.ebi.ac.uk/efo/EFO_0020838 GCST90101686 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ubiquitin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ubiquitin measurement http://www.ebi.ac.uk/efo/EFO_0020839 GCST90101687 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ubiquitin-conjugating enzyme E2 L3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ubiquitin-conjugating enzyme E2 L3 measurement http://www.ebi.ac.uk/efo/EFO_0020840 GCST90101688 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ubiquitin-conjugating enzyme E2 N levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ubiquitin-conjugating enzyme E2 N measurement http://www.ebi.ac.uk/efo/EFO_0020841 GCST90101689 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ubiquitin-fold modifier 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ubiquitin-fold modifier 1 measurement http://www.ebi.ac.uk/efo/EFO_0020842 GCST90101690 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ubiquitin-fold modifier-conjugating enzyme 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ubiquitin-fold modifier-conjugating enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020843 GCST90101691 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ubiquitin+1, truncated mutation for UbB levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ubiquitin+1, truncated mutation for UBB measurement http://www.ebi.ac.uk/efo/EFO_0020844 GCST90101692 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. UMP-CMP kinase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 UMP-CMP kinase measurement http://www.ebi.ac.uk/efo/EFO_0008313 GCST90101693 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Urokinase plasminogen activator surface receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90101694 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Urokinase-type plasminogen activator levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90101695 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vacuolar protein sorting-associated protein VTA1 homolog levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vacuolar protein sorting-associated protein VTA1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020845 GCST90101696 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vascular cell adhesion protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vascular cell adhesion protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020846 GCST90101697 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vascular endothelial growth factor A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90101698 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vascular endothelial growth factor A, isoform 121 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vascular endothelial growth factor A, isoform 121 measurement http://www.ebi.ac.uk/efo/EFO_0020847 GCST90101699 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vascular endothelial growth factor C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vascular endothelial growth factor C measurement http://www.ebi.ac.uk/efo/EFO_0020848 GCST90101700 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vascular endothelial growth factor receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90101701 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vascular endothelial growth factor receptor 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90101702 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vasoactive Intestinal Peptide levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vasoactive intestinal peptide measurement http://www.ebi.ac.uk/efo/EFO_0020849 GCST90101703 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vitamin K-dependent protein C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90101704 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Vitamin K-dependent protein S levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vitamin k-dependent protein S measurement http://www.ebi.ac.uk/efo/EFO_0020850 GCST90101705 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. von Willebrand factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90101706 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase BTK levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase BTK measurement http://www.ebi.ac.uk/efo/EFO_0020819 GCST90101666 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase CSK levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase CSK measurement http://www.ebi.ac.uk/efo/EFO_0020820 GCST90101667 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Fer levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase FER measurement http://www.ebi.ac.uk/efo/EFO_0020821 GCST90101668 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Fgr levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase FGR measurement http://www.ebi.ac.uk/efo/EFO_0020822 GCST90101669 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Fyn levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase FYN measurement http://www.ebi.ac.uk/efo/EFO_0020823 GCST90101670 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase HCK levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase HCK measurement http://www.ebi.ac.uk/efo/EFO_0020824 GCST90101671 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase JAK2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase JAK2 measurement http://www.ebi.ac.uk/efo/EFO_0020825 GCST90101672 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Lck levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90101673 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Lyn levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase lyn measurement http://www.ebi.ac.uk/efo/EFO_0020827 GCST90101674 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase Lyn, isoform B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase LYN, isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020828 GCST90101675 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase receptor Tie-1, soluble levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 tyrosine-protein kinase receptor Tie-1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008312 GCST90101676 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Apolipoprotein E (isoform E3) levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 apolipoprotein E (isoform E3) measurement http://www.ebi.ac.uk/efo/EFO_0020157 GCST90100668 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Apolipoprotein E (isoform E4) levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 apolipoprotein E (isoform E4) measurement http://www.ebi.ac.uk/efo/EFO_0020158 GCST90100669 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Apolipoprotein E levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90100670 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Apoptosis regulator Bcl-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 apoptosis regulator BCL-2 measurement http://www.ebi.ac.uk/efo/EFO_0020159 GCST90100671 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Arginase-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 arginase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020160 GCST90100672 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Aromatic-L-amino-acid decarboxylase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 aromatic-l-amino-acid decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0020161 GCST90100673 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Artemin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 artemin measurement http://www.ebi.ac.uk/efo/EFO_0020162 GCST90100674 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Arylsulfatase A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90100675 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Arylsulfatase B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 arylsulfatase B measurement http://www.ebi.ac.uk/efo/EFO_0008030 GCST90100676 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Asialoglycoprotein receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 asialoglycoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020164 GCST90100677 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Aspartate aminotransferase, cytoplasmic levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 aspartate aminotransferase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0008031 GCST90100678 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. AT-rich interactive domain-containing protein 3A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 AT-rich interactive domain-containing protein 3A measurement http://www.ebi.ac.uk/efo/EFO_0020165 GCST90100679 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. ATP synthase subunit beta, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ATP synthase subunit beta, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020166 GCST90100680 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. ATP-dependent RNA helicase DDX19B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ATP-dependent rna helicase ddx19b measurement http://www.ebi.ac.uk/efo/EFO_0020167 GCST90100681 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor-binding protein 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin-like growth factor-binding protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020477 GCST90101144 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor-binding protein 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin-like growth factor-binding protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020478 GCST90101145 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor-binding protein 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90101146 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Integrin alpha-I: beta-1 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 integrin alpha-I: beta-1 complex measurement http://www.ebi.ac.uk/efo/EFO_0008162 GCST90101147 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Integrin alpha-IIb: beta-3 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 integrin alpha-IIb: beta-3 complex measurement http://www.ebi.ac.uk/efo/EFO_0020479 GCST90101148 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Integrin alpha-V: beta-5 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 integrin alpha-V: beta-5 complex measurement http://www.ebi.ac.uk/efo/EFO_0020480 GCST90101149 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Inter-alpha-trypsin inhibitor heavy chain H4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 inter-alpha-trypsin inhibitor heavy chain h4 measurement http://www.ebi.ac.uk/efo/EFO_0020481 GCST90101150 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Intercellular adhesion molecule 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST90101151 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Intercellular adhesion molecule 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90101152 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Intercellular adhesion molecule 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 intercellular adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020482 GCST90101153 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Intercellular adhesion molecule 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90101154 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interferon alpha-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interferon alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020483 GCST90101155 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interferon gamma levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90101156 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interferon gamma receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interferon gamma receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020484 GCST90101157 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interferon lambda-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interferon lambda-1 measurement http://www.ebi.ac.uk/efo/EFO_0020485 GCST90101158 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interferon lambda-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interferon lambda-2 measurement http://www.ebi.ac.uk/efo/EFO_0020486 GCST90101159 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-1 alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST90101160 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-1 beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST90101161 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-1 Receptor accessory protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 interleukin 1 Receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008167 GCST90101162 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-1 receptor type 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90101163 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-1 receptor-like 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 6 interleukin 1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008168 GCST90101164 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-1 receptor-like 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 interleukin 1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0008169 GCST90101165 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-10 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90101166 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-10 receptor subunit beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-10 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020489 GCST90101167 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-11 measurement http://www.ebi.ac.uk/efo/EFO_0020490 GCST90101168 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Junctional adhesion molecule-like levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 junctional adhesion molecule-like measurement http://www.ebi.ac.uk/efo/EFO_0020511 GCST90101219 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. kallikrein-11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90101220 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 kallikrein-12 measurement http://www.ebi.ac.uk/efo/EFO_0008194 GCST90101221 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-13 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kallikrein-13 measurement http://www.ebi.ac.uk/efo/EFO_0020512 GCST90101222 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90101223 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kallikrein-4 measurement http://www.ebi.ac.uk/efo/EFO_0020514 GCST90101224 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90101225 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kallikrein‐6 measurement http://www.ebi.ac.uk/efo/EFO_0010622 GCST90101226 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 kallikrein-7 measurement http://www.ebi.ac.uk/efo/EFO_0008195 GCST90101227 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallikrein-8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90101228 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kallistatin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90101229 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Keratin, type I cytoskeletal 18 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 keratin, type I cytoskeletal 18 measurement http://www.ebi.ac.uk/efo/EFO_0020517 GCST90101230 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Killer cell immunoglobulin-like receptor 2DL4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90101231 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Killer cell immunoglobulin-like receptor 3DL2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 killer cell immunoglobulin-like receptor 3DL2 measurement http://www.ebi.ac.uk/efo/EFO_0020518 GCST90101232 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Killer cell immunoglobulin-like receptor 3DS1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 killer cell immunoglobulin-like receptor 3DS1 measurement http://www.ebi.ac.uk/efo/EFO_0020519 GCST90101233 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Killer cell lectin-like receptor subfamily F member 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 BCL-2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020177 GCST90101234 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kin of IRRE-like protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kin of IRRE-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020521 GCST90101235 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kinesin-like protein KIF23 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kinesin-like protein KIF23 measurement http://www.ebi.ac.uk/efo/EFO_0020522 GCST90101236 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kininogen-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 kininogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008198 GCST90101237 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kremen protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 kremen protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020523 GCST90101238 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kunitz-type protease inhibitor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 Kunitz-type protease inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008199 GCST90101239 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kunitz-type protease inhibitor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 Kunitz-type protease inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008200 GCST90101240 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Kynureninase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 kynureninase measurement http://www.ebi.ac.uk/efo/EFO_0008201 GCST90101241 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. L-lactate dehydrogenase B chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 L-lactate dehydrogenase B chain measurement http://www.ebi.ac.uk/efo/EFO_0020524 GCST90101242 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. L-selectin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90101243 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-11 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-11 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020491 GCST90101169 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 12 measurement http://www.ebi.ac.uk/efo/EFO_0004753 GCST90101170 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-12 receptor subunit beta-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90101171 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-12 receptor subunit beta-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-12 receptor subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020492 GCST90101172 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-13 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 13 measurement http://www.ebi.ac.uk/efo/EFO_0008171 GCST90101173 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-13 receptor subunit alpha-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-13 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020493 GCST90101174 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-15 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008172 GCST90101175 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-16 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 interleukin 16 measurement http://www.ebi.ac.uk/efo/EFO_0008173 GCST90101176 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-17 receptor A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90101177 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. interleukin-17 receptor B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 interleukin 17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0008176 GCST90101178 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-17 receptor C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-17 receptor c measurement http://www.ebi.ac.uk/efo/EFO_0020494 GCST90101179 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-17 receptor D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 17 receptor D measurement http://www.ebi.ac.uk/efo/EFO_0008177 GCST90101180 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-17A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90101181 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-17B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90101182 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-17D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90101183 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-17F levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90101184 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. interleukin-18 receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90101185 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-18 receptor accessory protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 18 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008179 GCST90101186 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-18-binding protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-18-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020495 GCST90101187 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-19 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 19 measurement http://www.ebi.ac.uk/efo/EFO_0008180 GCST90101188 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 2 measurement http://www.ebi.ac.uk/efo/EFO_0008331 GCST90101189 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-2 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 soluble interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0007650 GCST90101190 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-20 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-20 measurement http://www.ebi.ac.uk/efo/EFO_0020496 GCST90101191 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-20 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-20 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020497 GCST90101192 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-22 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90101193 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-22 receptor subunit alpha-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90101194 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-22 receptor subunit alpha-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90101195 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-23 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90101196 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-23 receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 23 receptor measurement http://www.ebi.ac.uk/efo/EFO_0008181 GCST90101197 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-24 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-24 measurement http://www.ebi.ac.uk/efo/EFO_0020502 GCST90101198 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-25 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 interleukin 25 measurement http://www.ebi.ac.uk/efo/EFO_0008182 GCST90101199 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-27 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-27 measurement http://www.ebi.ac.uk/efo/EFO_0010916 GCST90101200 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-27 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 27 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008183 GCST90101201 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020503 GCST90101202 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-3 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90101203 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-34 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-34 measurement http://www.ebi.ac.uk/efo/EFO_0020505 GCST90101204 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-37 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-37 measurement http://www.ebi.ac.uk/efo/EFO_0020506 GCST90101205 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 4 measurement http://www.ebi.ac.uk/efo/EFO_0008184 GCST90101206 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-4 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-4 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020507 GCST90101207 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 5 measurement http://www.ebi.ac.uk/efo/EFO_0008185 GCST90101208 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-5 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008186 GCST90101209 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90101210 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-6 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90101211 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-6 receptor subunit beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 6 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0008188 GCST90101212 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin 7 measurement http://www.ebi.ac.uk/efo/EFO_0008189 GCST90101213 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-7 receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interleukin 7 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008190 GCST90101214 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interleukin-8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST90101215 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Interstitial collagenase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 interstitial collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008193 GCST90101216 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Junctional adhesion molecule B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 junctional adhesion molecule B measurement http://www.ebi.ac.uk/efo/EFO_0020509 GCST90101217 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Junctional adhesion molecule C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 junctional adhesion molecule C measurement http://www.ebi.ac.uk/efo/EFO_0020510 GCST90101218 Genome-wide genotyping array 2022-02-21 34582791 Mikhaylova AV 2021-09-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34582791 Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. White blood cell count 14,246 African American individuals, 686 East Asian ancestry individuals, 33,285 European American ancestry individuals, 13,585 Hispanic/Latin American individuals 199,126 African ancestry, European ancestry, Hispanic or Latin American individuals NR [109563748] 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90094654 Genome-wide sequencing 2022-02-21 34582791 Mikhaylova AV 2021-09-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34582791 Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Basophil count 14,246 African American individuals, 686 East Asian ancestry individuals, 33,285 European American ancestry individuals, 13,585 Hispanic/Latin American individuals 199,126 African ancestry, European ancestry, Hispanic or Latin American individuals NR [87792529] 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90094655 Genome-wide sequencing 2022-02-21 34582791 Mikhaylova AV 2021-09-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34582791 Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Eosinophil counts 14,246 African American individuals, 686 East Asian ancestry individuals, 33,285 European American ancestry individuals, 13,585 Hispanic/Latin American individuals 199,126 African ancestry, European ancestry, Hispanic or Latin American individuals NR [88691872] 1 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90094656 Genome-wide sequencing 2022-02-21 34582791 Mikhaylova AV 2021-09-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34582791 Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Lymphocyte count 14,246 African American individuals, 686 East Asian ancestry individuals, 33,285 European American ancestry individuals, 13,585 Hispanic/Latin American individuals 199,126 African ancestry, European ancestry, Hispanic or Latin American individuals NR [94120287] 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90094657 Genome-wide sequencing 2022-02-21 34582791 Mikhaylova AV 2021-09-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34582791 Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Monocyte count 14,246 African American individuals, 686 East Asian ancestry individuals, 33,285 European American ancestry individuals, 13,585 Hispanic/Latin American individuals 199,126 African ancestry, European ancestry, Hispanic or Latin American individuals NR [93891280] 2 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90094658 Genome-wide sequencing 2022-02-21 34582791 Mikhaylova AV 2021-09-27 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34582791 Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program. Neutrophil count 14,246 African American individuals, 686 East Asian ancestry individuals, 33,285 European American ancestry individuals, 13,585 Hispanic/Latin American individuals 199,126 African ancestry, European ancestry, Hispanic or Latin American individuals NR [89259980] 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90094659 Genome-wide sequencing 2022-03-02 34271060 DeVore SB 2021-07-13 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34271060 Novel Role for Caspase Recruitment Domain Family Member 14 and its Genetic Variant rs11652075 in Skin Filaggrin Homeostasis. Lesional skin FLG expression levels in childhood atopic dermatitis 235 Black or unknown ancestry individuals NA Illumina [487523] 1 filaggrin gene expression measurement http://www.ebi.ac.uk/efo/EFO_0020899 GCST90094991 Genome-wide genotyping array 2022-03-02 34271060 DeVore SB 2021-07-13 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34271060 Novel Role for Caspase Recruitment Domain Family Member 14 and its Genetic Variant rs11652075 in Skin Filaggrin Homeostasis. Non(never)-lesional skin FLG expression levels in childhood atopic dermatitis 240 Black or unknown ancestry individuals NA Illumina [487523] 10 filaggrin gene expression measurement http://www.ebi.ac.uk/efo/EFO_0020899 GCST90094992 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transketolase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 transketolase measurement http://www.ebi.ac.uk/efo/EFO_0020783 GCST90101616 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Translationally-controlled tumor protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 translationally-controlled tumor protein measurement http://www.ebi.ac.uk/efo/EFO_0020784 GCST90101617 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transmembrane glycoprotein NMB levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90101618 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Trefoil factor 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90101619 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Triosephosphate isomerase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 triosephosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020785 GCST90101620 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tropomyosin alpha-1 chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tropomyosin alpha-1 chain measurement http://www.ebi.ac.uk/efo/EFO_0020786 GCST90101621 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tropomyosin beta chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tropomyosin beta chain measurement http://www.ebi.ac.uk/efo/EFO_0020787 GCST90101622 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Troponin I, cardiac muscle levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 troponin i, cardiac muscle measurement http://www.ebi.ac.uk/efo/EFO_0020788 GCST90101623 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Troponin I, fast skeletal muscle levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 troponin i, fast skeletal muscle measurement http://www.ebi.ac.uk/efo/EFO_0020789 GCST90101624 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Trypsin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 trypsin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020790 GCST90101625 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Trypsin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 trypsin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008305 GCST90101626 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Trypsin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 trypsin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020791 GCST90101627 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tryptase beta-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90101628 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tryptase gamma levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tryptase gamma measurement http://www.ebi.ac.uk/efo/EFO_0020792 GCST90101629 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90101630 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90101631 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 12 measurement http://www.ebi.ac.uk/efo/EFO_0010801 GCST90101632 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 13B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020793 GCST90101633 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90101634 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 15 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90101635 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 18 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020795 GCST90101636 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020796 GCST90101637 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 6, soluble form levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 6, soluble form measurement http://www.ebi.ac.uk/efo/EFO_0020797 GCST90101638 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90101639 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor ligand superfamily member 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor ligand superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0020798 GCST90101640 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Adapter molecule crk levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 adapter molecule CRK measurement http://www.ebi.ac.uk/efo/EFO_0020128 GCST90100618 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Adenylate kinase isoenzyme 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 adenylate kinase isoenzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020129 GCST90100619 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Adenylosuccinate lyase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 adenylosuccinate lyase measurement http://www.ebi.ac.uk/efo/EFO_0020130 GCST90100620 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Adiponectin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90100621 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 6 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90100622 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Advanced glycosylation end product-specific receptor, soluble levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 advanced glycosylation end product-specific receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0020131 GCST90100623 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Afamin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 afamin measurement http://www.ebi.ac.uk/efo/EFO_0008015 GCST90100624 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Aflatoxin B1 aldehyde reductase member 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 aflatoxin B1 aldehyde reductase member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020132 GCST90100625 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Aggrecan core protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 aggrecan core protein measurement http://www.ebi.ac.uk/efo/EFO_0020133 GCST90100626 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Agouti-related protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90100627 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. AH receptor-interacting protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 AH receptor-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0020134 GCST90100628 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alanine aminotransferase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90100629 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alcohol dehydrogenase [NADP(+)] levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 alcohol dehydrogenase [NADP+] measurement http://www.ebi.ac.uk/efo/EFO_0008017 GCST90100630 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alkaline phosphatase, tissue-nonspecific isozyme levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90100631 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Allograft inflammatory factor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 allograft inflammatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020135 GCST90100632 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-(1,3)-fucosyltransferase 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90100633 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. alpha-1-antichymotrypsin complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 alpha-1-antichymotrypsin complex measurement http://www.ebi.ac.uk/efo/EFO_0008018 GCST90100634 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-1-antichymotrypsin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 alpha-1-antichymotrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008019 GCST90100635 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-1-antitrypsin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008327 GCST90100636 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-2-antiplasmin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 alpha-2-antiplasmin measurement http://www.ebi.ac.uk/efo/EFO_0020137 GCST90100637 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-2-HS-glycoprotein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90100638 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-2-macroglobulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 alpha-2-macroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020138 GCST90100639 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. alpha-2-macroglobulin receptor-associated protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90100640 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-L-iduronidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90100641 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Alpha-soluble NSF attachment protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 alpha-soluble NSF attachment protein measurement http://www.ebi.ac.uk/efo/EFO_0020140 GCST90100642 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thymidine kinase, cytosolic levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thymidine kinase, cytosolic measurement http://www.ebi.ac.uk/efo/EFO_0020773 GCST90101599 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thymidylate synthase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thymidylate synthase measurement http://www.ebi.ac.uk/efo/EFO_0020774 GCST90101600 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thyroglobulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thyroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010050 GCST90101601 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thyroid peroxidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thyroid peroxidase measurement http://www.ebi.ac.uk/efo/EFO_0020775 GCST90101602 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thyroid stimulating hormone levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST90101603 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thyroxine-Binding Globulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thyroxine-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0009172 GCST90101604 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tissue factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tissue factor measurement http://www.ebi.ac.uk/efo/EFO_0010623 GCST90101605 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tissue factor pathway inhibitor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90101606 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tissue-type plasminogen activator levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tissue-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0020776 GCST90101607 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Toll-like receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 toll-like receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020777 GCST90101608 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Toll-like receptor 4:Lymphocyte antigen 96 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90101609 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transcription factor IIIB 90 kDa subunit levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 transcription factor IIIb 90 kda subunit measurement http://www.ebi.ac.uk/efo/EFO_0020778 GCST90101610 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transforming growth factor beta receptor type 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 transforming growth factor beta receptor type 3 measurement http://www.ebi.ac.uk/efo/EFO_0020779 GCST90101611 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transforming growth factor beta-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 transforming growth factor beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020780 GCST90101612 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transforming growth factor beta-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 transforming growth factor beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020781 GCST90101613 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transforming growth factor beta-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 transforming growth factor beta-3 measurement http://www.ebi.ac.uk/efo/EFO_0020782 GCST90101614 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Transforming growth factor-beta-induced protein ig-h3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 transforming growth factor-beta-induced protein ig-h3 measurement http://www.ebi.ac.uk/efo/EFO_0008302 GCST90101615 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 15 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 a disintegrin and metalloproteinase with thrombospondin motifs 15 measurement http://www.ebi.ac.uk/efo/EFO_0020123 GCST90100610 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 a disintegrin and metalloproteinase with thrombospondin motifs 4 measurement http://www.ebi.ac.uk/efo/EFO_0020124 GCST90100611 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90100612 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Abelson tyrosine-protein kinase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 Abelson tyrosine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008012 GCST90100613 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Acid sphingomyelinase-like phosphodiesterase 3a levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90100614 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Acidic leucine-rich nuclear phosphoprotein 32 family member B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90100615 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Activated Protein C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 activated protein C measurement http://www.ebi.ac.uk/efo/EFO_0020126 GCST90100616 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Activin receptor type-1B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 activin receptor type-1B measurement http://www.ebi.ac.uk/efo/EFO_0020127 GCST90100617 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Aminoacylase-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 aminoacylase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020141 GCST90100643 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. AMP Kinase (alpha1beta1gamma1) levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 amp kinase (alpha1beta1gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020142 GCST90100644 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. AMP Kinase (alpha2beta2gamma1) levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 amp kinase (alpha2beta2gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020143 GCST90100645 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Amphiregulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 amphiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020144 GCST90100646 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Amyloid beta A4 protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 amyloid beta A4 protein measurement http://www.ebi.ac.uk/efo/EFO_0020145 GCST90100647 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiogenin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90100648 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiopoietin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 angiopoietin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020146 GCST90100649 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiopoietin-1 receptor, soluble levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 angiopoietin-1 receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008023 GCST90100650 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiopoietin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90100651 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiopoietin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 angiopoietin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020147 GCST90100652 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiopoietin-related protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 angiopoietin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020148 GCST90100653 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiopoietin-related protein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 angiopoietin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020149 GCST90100654 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiostatin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 angiostatin measurement http://www.ebi.ac.uk/efo/EFO_0008024 GCST90100655 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiotensin-converting enzyme 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 angiotensin-converting enzyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0020150 GCST90100656 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Angiotensinogen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 angiotensinogen measurement http://www.ebi.ac.uk/efo/EFO_0008025 GCST90100657 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Annexin A1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 annexin A1 measurement http://www.ebi.ac.uk/efo/EFO_0008026 GCST90100658 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Annexin A2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 annexin A2 measurement http://www.ebi.ac.uk/efo/EFO_0008027 GCST90100659 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Annexin A6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 annexin A6 measurement http://www.ebi.ac.uk/efo/EFO_0020151 GCST90100660 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Anterior gradient protein 2 homolog levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 anterior gradient protein 2 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020152 GCST90100661 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Anti-Muellerian hormone type-2 receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 anti-muellerian hormone type-2 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020153 GCST90100662 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Antileukoproteinase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 antileukoproteinase measurement http://www.ebi.ac.uk/efo/EFO_0020154 GCST90100663 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Antithrombin-III levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 antithrombin-III measurement http://www.ebi.ac.uk/efo/EFO_0020155 GCST90100664 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Apolipoprotein B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90100665 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Apolipoprotein D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90100666 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Apolipoprotein E (isoform E2) levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 apolipoprotein E isoform E2 measurement http://www.ebi.ac.uk/efo/EFO_0008028 GCST90100667 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 10A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 10A measurement http://www.ebi.ac.uk/efo/EFO_0020799 GCST90101641 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 11A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 11A measurement http://www.ebi.ac.uk/efo/EFO_0020800 GCST90101642 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 11B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 11B measurement http://www.ebi.ac.uk/efo/EFO_0020801 GCST90101643 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 12A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 12A measurement http://www.ebi.ac.uk/efo/EFO_0020802 GCST90101644 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 13B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020803 GCST90101645 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 13C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 13C measurement http://www.ebi.ac.uk/efo/EFO_0020804 GCST90101646 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0020805 GCST90101647 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 17 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 17 measurement http://www.ebi.ac.uk/efo/EFO_0020806 GCST90101648 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 18 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020807 GCST90101649 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 19 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 19 measurement http://www.ebi.ac.uk/efo/EFO_0020808 GCST90101650 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 19L levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90101651 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 1A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 1Ameasurement http://www.ebi.ac.uk/efo/EFO_0020809 GCST90101652 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 1B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90101653 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 21 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 21 measurement http://www.ebi.ac.uk/efo/EFO_0020810 GCST90101654 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 25 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 25 measurement http://www.ebi.ac.uk/efo/EFO_0020811 GCST90101655 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 27 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 27 measurement http://www.ebi.ac.uk/efo/EFO_0020812 GCST90101656 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 3 measurement http://www.ebi.ac.uk/efo/EFO_0020813 GCST90101657 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020814 GCST90101658 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 6B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 6B measurement http://www.ebi.ac.uk/efo/EFO_0020815 GCST90101659 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0020816 GCST90101660 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90101661 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor receptor superfamily member EDAR levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 tumor necrosis factor receptor superfamily member EDAR measurement http://www.ebi.ac.uk/efo/EFO_0008310 GCST90101662 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor necrosis factor-inducible gene 6 protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 tumor necrosis factor-inducible gene 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0008311 GCST90101663 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tumor-associated calcium signal transducer 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tumor-associated calcium signal transducer 2 measurement http://www.ebi.ac.uk/efo/EFO_0020817 GCST90101664 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tyrosine-protein kinase ABL1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tyrosine-protein kinase ABL1 measurement http://www.ebi.ac.uk/efo/EFO_0020818 GCST90101665 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. MAP kinase-activated protein kinase 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 MAP kinase-activated protein kinase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020553 GCST90101294 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mast/stem cell growth factor receptor Kit levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mast/stem cell growth factor receptor kit measurement http://www.ebi.ac.uk/efo/EFO_0020554 GCST90101295 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrilin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 matrilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020555 GCST90101296 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrilin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 matrilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020556 GCST90101297 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrilysin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 matrilysin measurement http://www.ebi.ac.uk/efo/EFO_0008227 GCST90101298 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrix extracellular phosphoglycoprotein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 matrix extracellular phosphoglycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020557 GCST90101299 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrix metalloproteinase-14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 matrix metalloproteinase-14 measurement http://www.ebi.ac.uk/efo/EFO_0020558 GCST90101300 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrix metalloproteinase-16 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 matrix metalloproteinase-16 measurement http://www.ebi.ac.uk/efo/EFO_0020559 GCST90101301 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrix metalloproteinase-17 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 matrix metalloproteinase-17 measurement http://www.ebi.ac.uk/efo/EFO_0020560 GCST90101302 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Matrix metalloproteinase-9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 matrix metalloproteinase-9 measurement http://www.ebi.ac.uk/efo/EFO_0020561 GCST90101303 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mediator of RNA polymerase II transcription subunit 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90101304 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Megakaryocyte-associated tyrosine-protein kinase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 megakaryocyte-associated tyrosine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0020562 GCST90101305 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. melanoma-derived growth regulatory protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 6 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90101306 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Membrane frizzled-related protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 membrane frizzled-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020563 GCST90101307 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Membrane metallo-endopeptidase-like 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 membrane metallo-endopeptidase-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020564 GCST90101308 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mesothelin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mesothelin measurement http://www.ebi.ac.uk/efo/EFO_0020565 GCST90101309 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Metalloproteinase inhibitor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 metalloproteinase inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020566 GCST90101310 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Metalloproteinase inhibitor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 metalloproteinase inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020567 GCST90101311 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Metalloproteinase inhibitor 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 7 metalloproteinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008231 GCST90101312 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Methionine aminopeptidase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 methionine aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020568 GCST90101313 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Methionine aminopeptidase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 methionine aminopeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008232 GCST90101314 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Methyl-CpG-binding domain protein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 methyl-cpg-binding domain protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020569 GCST90101315 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. MHC class I polypeptide-related sequence A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 19 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST90101316 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. MHC class I polypeptide-related sequence B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 11 MHC class I polypeptide-related sequence B measurement http://www.ebi.ac.uk/efo/EFO_0008234 GCST90101317 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lactadherin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 lactadherin measurement http://www.ebi.ac.uk/efo/EFO_0008203 GCST90101244 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lactoperoxidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lactoperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0020525 GCST90101245 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lactotransferrin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lactotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020526 GCST90101246 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lamin-B1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lamin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020527 GCST90101247 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Laminin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 laminin measurement http://www.ebi.ac.uk/efo/EFO_0020528 GCST90101248 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Layilin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 layilin measurement http://www.ebi.ac.uk/efo/EFO_0020529 GCST90101249 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Legumain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 legumain measurement http://www.ebi.ac.uk/efo/EFO_0020530 GCST90101250 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leptin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90101251 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leptin receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90101252 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leucine carboxyl methyltransferase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 leucine carboxyl methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008207 GCST90101253 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leucine-rich repeat transmembrane neuronal protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 leucine-rich repeat transmembrane neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020531 GCST90101254 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leucine-rich repeat transmembrane neuronal protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 leucine-rich repeat transmembrane neuronal protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020532 GCST90101255 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leucine-rich repeat transmembrane protein FLRT1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 leucine-rich repeat transmembrane protein FLRT1 measurement http://www.ebi.ac.uk/efo/EFO_0020533 GCST90101256 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leucine-rich repeats and immunoglobulin-like domains protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 leucine-rich repeats and immunoglobulin-like domains protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020534 GCST90101257 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leukemia inhibitory factor receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90101258 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90101259 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leukocyte immunoglobulin-like receptor subfamily B member 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90101260 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Leukotriene A-4 hydrolase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 leukotriene a-4 hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020535 GCST90101261 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ligand-dependent nuclear receptor corepressor-like protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ligand-dependent nuclear receptor corepressor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020536 GCST90101262 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Limbic system-associated membrane protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 limbic system-associated membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0020537 GCST90101263 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Low affinity immunoglobulin epsilon Fc receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 low affinity immunoglobulin epsilon Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0008210 GCST90101264 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Low affinity immunoglobulin gamma Fc region receptor II-a/b levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 6 low affinity immunoglobulin gamma Fc region receptor II-a/b measurement http://www.ebi.ac.uk/efo/EFO_0008211 GCST90101265 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Low affinity immunoglobulin gamma Fc region receptor III-B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 low affinity immunoglobulin gamma Fc region receptor III-B measurement http://www.ebi.ac.uk/efo/EFO_0008212 GCST90101266 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Low molecular weight phosphotyrosine protein phosphatase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90101267 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Low-density lipoprotein receptor-related protein 8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 low-density lipoprotein receptor-related protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0020538 GCST90101268 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Luteinizing hormone levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90101269 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lymphatic vessel endothelial hyaluronic acid receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lymphatic vessel endothelial hyaluronic acid receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020539 GCST90101270 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lymphocyte activation gene 3 protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lymphocyte activation gene 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0020540 GCST90101271 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lymphocyte antigen 86 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lymphocyte antigen 86 measurement http://www.ebi.ac.uk/efo/EFO_0020541 GCST90101272 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lymphotactin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 lymphotactin measurement http://www.ebi.ac.uk/efo/EFO_0008214 GCST90101273 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lymphotoxin alpha1:beta2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lymphotoxin alpha1:beta2 measurement http://www.ebi.ac.uk/efo/EFO_0020542 GCST90101274 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lymphotoxin alpha2:beta1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lymphotoxin alpha2:beta1 measurement http://www.ebi.ac.uk/efo/EFO_0020543 GCST90101275 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lymphotoxin-alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lymphotoxin-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020544 GCST90101276 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lysosomal protective protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90101277 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lysosome membrane protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 lysosome membrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020545 GCST90101278 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Lysozyme C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90101279 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage colony-stimulating factor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 macrophage colony-stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020546 GCST90101280 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage colony-stimulating factor 1 receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 macrophage colony-stimulating factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020547 GCST90101281 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage mannose receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 macrophage mannose receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020548 GCST90101282 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage metalloelastase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 macrophage metalloelastase measurement http://www.ebi.ac.uk/efo/EFO_0008220 GCST90101283 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage Migration Inhibitory Factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST90101284 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage scavenger receptor types I and II levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90101285 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage-capping protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 macrophage-capping protein measurement http://www.ebi.ac.uk/efo/EFO_0020549 GCST90101286 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Macrophage-stimulating protein receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 macrophage-stimulating protein receptor measurement http://www.ebi.ac.uk/efo/EFO_0020550 GCST90101287 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Malate dehydrogenase, cytoplasmic levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 malate dehydrogenase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020551 GCST90101288 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mammaglobin-B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mammaglobin-b measurement http://www.ebi.ac.uk/efo/EFO_0020552 GCST90101289 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mannan-binding lectin serine protease 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90101290 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mannose-binding protein C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 mannose-binding protein C measurement http://www.ebi.ac.uk/efo/EFO_0008224 GCST90101291 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. MAP kinase-activated protein kinase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 MAP kinase-activated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008225 GCST90101292 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. MAP kinase-activated protein kinase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90101293 Genome-wide genotyping array 2021-12-23 32439431 Simard M 2020-05-19 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/32439431 Polygenic risk score for atopic dermatitis in the Canadian population. Atopic dermatitis (moderate to severe) 222 South East Asian ancestry, East Asian ancestry, South Asian ancestry, African American or Afro-Caribbean, European ancestry, Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 2,466 Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, NR moderate to severe atopic dermatitis cases, 2,466 South East Asian ancestry, East Asian ancestry, South Asian ancestry, African American or Afro-Caribbean, European ancestry, Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 2,466 Greater Middle Eastern (Middle Eastern, North African or Persian), Hispanic or Latin American, NR controls without moderate to severe atopic dermatitis NA Illumina [5894709] (imputed) 25 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90086172 Genome-wide genotyping array 2022-02-24 34728798 Sanchez-Roige S 2021-11-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34728798 Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry. Problematic opioid prescription use 27,805 European ancestry cases, 104,308 European ancestry controls NA Illumina [11311983] (imputed) 2 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90094988 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Natural cytotoxicity triggering receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90101343 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Natural cytotoxicity triggering receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 natural cytotoxicity triggering receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020589 GCST90101344 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Natural cytotoxicity triggering receptor 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 natural cytotoxicity triggering receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008243 GCST90101345 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Netrin receptor UNC5C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 netrin receptor UNC5C measurement http://www.ebi.ac.uk/efo/EFO_0020590 GCST90101346 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Netrin receptor UNC5D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90101347 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurexin-1-beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neurexin-1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020596 GCST90101352 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurexin-3-beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neurexin-3-beta measurement http://www.ebi.ac.uk/efo/EFO_0020597 GCST90101353 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurexophilin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90101354 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurogenic locus notch homolog protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 neurogenic locus notch homolog protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008246 GCST90101356 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neuropilin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neuropilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020603 GCST90101361 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neutrophil elastase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neutrophil elastase measurement http://www.ebi.ac.uk/efo/EFO_0020605 GCST90101366 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Microtubule-associated protein tau levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 microtubule-associated protein tau measurement http://www.ebi.ac.uk/efo/EFO_0020570 GCST90101318 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Midkine levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 midkine measurement http://www.ebi.ac.uk/efo/EFO_0020571 GCST90101319 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitochondrial glutamate carrier 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitochondrial glutamate carrier 2 measurement http://www.ebi.ac.uk/efo/EFO_0020572 GCST90101320 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitochondrial import inner membrane translocase subunit TIM14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitochondrial import inner membrane translocase subunit tim14 measurement http://www.ebi.ac.uk/efo/EFO_0020573 GCST90101321 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020574 GCST90101322 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 11 measurement http://www.ebi.ac.uk/efo/EFO_0020575 GCST90101323 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 12 measurement http://www.ebi.ac.uk/efo/EFO_0020576 GCST90101324 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 13 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 13 measurement http://www.ebi.ac.uk/efo/EFO_0020577 GCST90101325 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 14 measurement http://www.ebi.ac.uk/efo/EFO_0020578 GCST90101326 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020579 GCST90101327 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020580 GCST90101328 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020581 GCST90101329 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Mitogen-activated protein kinase kinase kinase 7:TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 fusion levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 mitogen-activated protein kinase kinase kinase 7:tgf-beta-activated kinase 1 and map3k7-binding protein 1 fusion measurement http://www.ebi.ac.uk/efo/EFO_0020582 GCST90101330 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Moesin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 moesin measurement http://www.ebi.ac.uk/efo/EFO_0020583 GCST90101331 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Muellerian-inhibiting factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 muellerian-inhibiting factor measurement http://www.ebi.ac.uk/efo/EFO_0020584 GCST90101332 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Myeloblastin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90101333 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Myeloid cell surface antigen CD33 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90101334 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Myeloperoxidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90101335 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Myoglobin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 myoglobin measurement http://www.ebi.ac.uk/efo/EFO_0005057 GCST90101336 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. N-acetyl-D-glucosamine kinase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 N-acetyl-D-glucosamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0008239 GCST90101337 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. N-acetylglucosamine-6-sulfatase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90101338 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. N-acylethanolamine-hydrolyzing acid amidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90101339 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NAD-dependent protein deacetylase sirtuin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 NAD-dependent protein deacetylase sirtuin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008241 GCST90101340 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NADPH--cytochrome P450 reductase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 NADPH--cytochrome P450 reductase measurement http://www.ebi.ac.uk/efo/EFO_0008242 GCST90101341 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Nascent polypeptide-associated complex subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 nascent polypeptide-associated complex subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020587 GCST90101342 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Netrin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 netrin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020592 GCST90101348 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neural cell adhesion molecule 1, 120 kDa isoform levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neural cell adhesion molecule 1, 120 kda isoform measurement http://www.ebi.ac.uk/efo/EFO_0020593 GCST90101349 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neural cell adhesion molecule L1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neural cell adhesion molecule L1 measurement http://www.ebi.ac.uk/efo/EFO_0020594 GCST90101350 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neural cell adhesion molecule L1-like protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neural cell adhesion molecule l1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020595 GCST90101351 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neuroblastoma suppressor of tumorigenicity 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neuroblastoma suppressor of tumorigenicity 1 measurement http://www.ebi.ac.uk/efo/EFO_0020598 GCST90101355 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurogenic locus notch homolog protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90101357 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurogenic locus notch homolog protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neurogenic locus notch homolog protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020600 GCST90101358 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neuroligin-4, X-linked levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neuroligin-4, x-linked measurement http://www.ebi.ac.uk/efo/EFO_0020601 GCST90101359 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neuronal cell adhesion molecule levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neuronal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020602 GCST90101360 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurotrophin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neurotrophin-3 measurement http://www.ebi.ac.uk/efo/EFO_0010791 GCST90101362 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neurotrophin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neurotrophin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020604 GCST90101363 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neutral ceramidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90101364 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neutrophil collagenase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 neutrophil collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008248 GCST90101365 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Neutrophil-activating peptide 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 neutrophil-activating peptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020606 GCST90101367 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. VPS10 domain-containing receptor SorCS2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 vps10 domain-containing receptor sorcs2 measurement http://www.ebi.ac.uk/efo/EFO_0020851 GCST90101707 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. WAP, kazal, immunoglobulin, kunitz and NTR domain-containing protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 wap, kazal, immunoglobulin, kunitz and ntr domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020852 GCST90101708 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90101709 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Wnt inhibitory factor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 wnt inhibitory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020853 GCST90101710 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. WNT1-inducible-signaling pathway protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 WNT1-inducible-signaling pathway protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008321 GCST90101711 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. X-linked interleukin-1 receptor accessory protein-like 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 x-linked interleukin-1 receptor accessory protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0020854 GCST90101712 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. X-ray repair cross-complementing protein 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 x-ray repair cross-complementing protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020855 GCST90101713 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Xaa-Pro aminopeptidase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 xaa-pro aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020856 GCST90101714 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 22 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90100727 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 23 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90100728 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 24 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-C motif chemokine 24 measurement http://www.ebi.ac.uk/efo/EFO_0020197 GCST90100729 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 25 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90100730 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 27 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-C motif chemokine 27 measurement http://www.ebi.ac.uk/efo/EFO_0020198 GCST90100731 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 28 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-C motif chemokine 28 measurement http://www.ebi.ac.uk/efo/EFO_0020199 GCST90100732 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 C-C motif chemokine 3 measurement http://www.ebi.ac.uk/efo/EFO_0008051 GCST90100733 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 3-like 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-C motif chemokine 3-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008052 GCST90100734 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 4-like levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90100735 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008053 GCST90100736 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST90100737 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-C motif chemokine 8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 C-C motif chemokine 8 measurement http://www.ebi.ac.uk/efo/EFO_0008055 GCST90100738 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-reactive protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90100739 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-type lectin domain family 1 member B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-type lectin domain family 1 member B measurement http://www.ebi.ac.uk/efo/EFO_0020200 GCST90100740 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-type lectin domain family 4 member K levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-type lectin domain family 4 member K measurement http://www.ebi.ac.uk/efo/EFO_0020201 GCST90100741 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-type lectin domain family 4 member M levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-type lectin domain family 4 member M measurement http://www.ebi.ac.uk/efo/EFO_0020202 GCST90100742 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-type lectin domain family 7 member A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-type lectin domain family 4 member K measurement http://www.ebi.ac.uk/efo/EFO_0020201 GCST90100743 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-type mannose receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-type mannose receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020204 GCST90100744 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-X-C motif chemokine 10 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST90100745 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-X-C motif chemokine 11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90100746 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-X-C motif chemokine 13 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-X-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020205 GCST90100747 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-X-C motif chemokine 16 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90100748 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-X-C motif chemokine 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 C-X-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008058 GCST90100749 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C-X-C motif chemokine 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90100750 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C3a anaphylatoxin des Arginine levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C3a anaphylatoxin des arginine measurement http://www.ebi.ac.uk/efo/EFO_0020206 GCST90100751 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C3a anaphylatoxin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C3a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020207 GCST90100752 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. C5a anaphylatoxin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 C5a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020208 GCST90100753 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cadherin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90100754 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cadherin-12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cadherin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020210 GCST90100755 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cadherin-15 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0020211 GCST90100756 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cadherin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cadherin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020212 GCST90100757 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cadherin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cadherin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020213 GCST90100758 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cadherin-5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 cadherin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008060 GCST90100759 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cadherin-6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cadherin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020214 GCST90100760 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcineurin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 calcineurin measurement http://www.ebi.ac.uk/efo/EFO_0008061 GCST90100761 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcineurin subunit B type 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 calcineurin subunit B type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020215 GCST90100762 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcium-dependent phospholipase A2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 calcium-dependent phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020216 GCST90100763 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcium/calmodulin-dependent protein kinase kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 calcium/calmodulin-dependent protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020217 GCST90100764 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcium/calmodulin-dependent protein kinase type 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 calcium/calmodulin-dependent protein kinase type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008062 GCST90100765 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcium/calmodulin-dependent protein kinase type 1D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90100766 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcium/calmodulin-dependent protein kinase type II subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 calcium/calmodulin-dependent protein kinase type II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020218 GCST90100767 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcium/calmodulin-dependent protein kinase type II subunit beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 calcium/calmodulin-dependent protein kinase type II subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020219 GCST90100768 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calcium/calmodulin-dependent protein kinase type II subunit delta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 calcium/calmodulin-dependent protein kinase type II subunit delta measurement http://www.ebi.ac.uk/efo/EFO_0020220 GCST90100769 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calpain I levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 calpain I measurement http://www.ebi.ac.uk/efo/EFO_0008064 GCST90100770 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calpastatin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 calpastatin measurement http://www.ebi.ac.uk/efo/EFO_0008065 GCST90100771 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Calreticulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 calreticulin measurement http://www.ebi.ac.uk/efo/EFO_0020221 GCST90100772 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. cAMP-dependent protein kinase catalytic subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cAMP-dependent protein kinase catalytic subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020222 GCST90100773 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. cAMP-regulated phosphoprotein 19 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cAMP-regulated phosphoprotein 19 measurement http://www.ebi.ac.uk/efo/EFO_0020223 GCST90100774 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. cAMP-specific 3',5'-cyclic phosphodiesterase 4D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cAMP-specific 3',5'-cyclic phosphodiesterase 4D measurement http://www.ebi.ac.uk/efo/EFO_0020224 GCST90100775 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbohydrate sulfotransferase 15 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90100776 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbohydrate sulfotransferase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbohydrate sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020225 GCST90100777 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbohydrate sulfotransferase 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbohydrate sulfotransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020226 GCST90100778 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbonic anhydrase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020227 GCST90100779 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 13 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 carbonic anhydrase 13 measurement http://www.ebi.ac.uk/efo/EFO_0008067 GCST90100780 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbonic anhydrase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020228 GCST90100781 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbonic anhydrase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020229 GCST90100782 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbonic anhydrase 4 measurement http://www.ebi.ac.uk/efo/EFO_0020230 GCST90100783 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 carbonic anhydrase 6 measurement http://www.ebi.ac.uk/efo/EFO_0008068 GCST90100784 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbonic anhydrase 7 measurement http://www.ebi.ac.uk/efo/EFO_0020231 GCST90100785 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbonic anhydrase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020232 GCST90100786 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carbonic anhydrase-related protein 10 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carbonic anhydrase-related protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020233 GCST90100787 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carboxypeptidase B2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 carboxypeptidase B2 measurement http://www.ebi.ac.uk/efo/EFO_0008069 GCST90100788 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Carboxypeptidase E levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 carboxypeptidase e measurement http://www.ebi.ac.uk/efo/EFO_0020234 GCST90100789 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cardiotrophin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cardiotrophin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020235 GCST90100790 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Casein kinase II 2-alpha:2-beta heterotetramer levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 casein kinase II 2-alpha:2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020236 GCST90100791 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Casein kinase II 2-alpha':2-beta heterotetramer levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 casein kinase II 2-alpha':2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020237 GCST90100792 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Casein kinase II subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 casein kinase II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020238 GCST90100793 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Caspase-10 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 caspase-10 measurement http://www.ebi.ac.uk/efo/EFO_0020239 GCST90100794 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Caspase-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 caspase-2 measurement http://www.ebi.ac.uk/efo/EFO_0020240 GCST90100795 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Caspase-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 caspase-3 measurement http://www.ebi.ac.uk/efo/EFO_0008070 GCST90100796 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Catalase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 catalase measurement http://www.ebi.ac.uk/efo/EFO_0008071 GCST90100797 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90100798 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cathepsin D measurement http://www.ebi.ac.uk/efo/EFO_0010611 GCST90100799 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin E levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cathepsin E measurement http://www.ebi.ac.uk/efo/EFO_0020241 GCST90100800 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin G levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cathepsin G measurement http://www.ebi.ac.uk/efo/EFO_0020242 GCST90100801 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin H levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90100802 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin L2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cathepsin L2 measurement http://www.ebi.ac.uk/efo/EFO_0020244 GCST90100803 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin S levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90100804 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cathepsin Z levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 cathepsin Z measurement http://www.ebi.ac.uk/efo/EFO_0008074 GCST90100805 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cation-independent mannose-6-phosphate receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90100806 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD109 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 CD109 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008076 GCST90100807 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD166 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 CD166 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020245 GCST90100808 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD209 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90100809 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD226 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 CD226 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020246 GCST90100810 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD27 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 CD27 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008078 GCST90100811 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD40 ligand levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST90100812 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD48 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 CD48 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020247 GCST90100813 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD5 antigen-like levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 CD5 antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0020248 GCST90100814 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD70 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 CD70 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020249 GCST90100815 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CD97 antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 CD97 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020250 GCST90100816 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cell adhesion molecule 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0020251 GCST90100817 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cell adhesion molecule 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cell adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020252 GCST90100818 Genome-wide genotyping array 2022-02-22 35047847 Miao Z 2021-08-24 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35047847 Identification of 90 NAFLD GWAS loci and establishment of NAFLD PRS and causal role of NAFLD in coronary artery disease. Nonalcoholic fatty liver disease (imputed) 28,396 European ancestry cases, 108,652 European ancestry controls NA NR [NR] 94 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90094908 Genome-wide genotyping array 2022-02-22 35047847 Miao Z 2021-08-24 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35047847 Identification of 90 NAFLD GWAS loci and establishment of NAFLD PRS and causal role of NAFLD in coronary artery disease. Coronary artery disease 17,188 European ancestry cases, 110,447 European ancestry controls NA NR [NR] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90094909 Genome-wide genotyping array 2022-02-22 35047847 Miao Z 2021-08-24 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35047847 Identification of 90 NAFLD GWAS loci and establishment of NAFLD PRS and causal role of NAFLD in coronary artery disease. Nonalcoholic fatty liver disease 2,181 European ancestry cases, 2,444 European ancestry controls NA NR [NR] 2 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90094907 Genome-wide genotyping array 2022-02-24 34626176 Malik R 2021-10-01 Brain www.ncbi.nlm.nih.gov/pubmed/34626176 Whole-exome sequencing reveals a role of HTRA1 and EGFL8 in brain white matter hyperintensities. White matter hyperintensity volume 17,830 individuals NA NR [NR] 4 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST90094986 Exome-wide sequencing 2022-02-22 35132056 Mitchell BL 2022-02-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35132056 Genome-wide association meta-analysis identifies 29 new acne susceptibility loci. acne vulgaris 20,165 European ancestry cases, 595,231 European ancestry controls NA Affymetrix, Illumina [7072771] (imputed) 46 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST90092000 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serum amyloid A-1 protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90101543 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serum amyloid P-component levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 serum amyloid P-component measurement http://www.ebi.ac.uk/efo/EFO_0008283 GCST90101544 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serum paraoxonase/arylesterase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serum paraoxonase/arylesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020736 GCST90101545 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sex hormone-binding globulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90101546 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SH2 domain-containing protein 1A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sh2 domain-containing protein 1a measurement http://www.ebi.ac.uk/efo/EFO_0020737 GCST90101547 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SHC-transforming protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 shc-transforming protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020738 GCST90101548 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sialic acid-binding Ig-like lectin 14 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90101549 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sialic acid-binding Ig-like lectin 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 sialic acid-binding Ig-like lectin 6 measurement http://www.ebi.ac.uk/efo/EFO_0008285 GCST90101550 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sialic acid-binding Ig-like lectin 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90101551 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sialic acid-binding Ig-like lectin 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 sialic acid-binding Ig-like lectin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008286 GCST90101552 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sialoadhesin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sialoadhesin measurement http://www.ebi.ac.uk/efo/EFO_0020740 GCST90101553 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SLAM family member 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90101554 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SLAM family member 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 SLAM family member 6 measurement http://www.ebi.ac.uk/efo/EFO_0020742 GCST90101555 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SLAM family member 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90101556 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C4b levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 complement C4b measurement http://www.ebi.ac.uk/efo/EFO_0008092 GCST004365 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 [Pyruvate dehydrogenase acetyl-transferring] kinase isozyme 1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008010 GCST90100592 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 measurement http://www.ebi.ac.uk/efo/EFO_0020108 GCST90100593 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 14-3-3 protein family levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 14-3-3 protein family measurement http://www.ebi.ac.uk/efo/EFO_0020109 GCST90100594 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 14-3-3 protein sigma levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 14-3-3 protein sigma measurement http://www.ebi.ac.uk/efo/EFO_0020110 GCST90100595 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 15-hydroxyprostaglandin dehydrogenase [NAD(+)] levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 15-hydroxyprostaglandin dehydrogenase [NAD(+)] measurement http://www.ebi.ac.uk/efo/EFO_0020111 GCST90100596 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 26S proteasome non-ATPase regulatory subunit 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 26s proteasome non-atpase regulatory subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0020112 GCST90100597 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 3-hydroxy-3-methylglutaryl-coenzyme A reductase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 3-hydroxy-3-methylglutaryl-coenzymeAreductase measurement http://www.ebi.ac.uk/efo/EFO_0020113 GCST90100598 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 3-hydroxyacyl-CoA dehydrogenase type-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 3-hydroxyacyl-coa dehydrogenase type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020114 GCST90100599 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 3-hydroxyisobutyrate dehydrogenase, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 3-hydroxyisobutyrate dehydrogenase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020115 GCST90100600 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 3-phosphoinositide-dependent protein kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 3-phosphoinositide-dependent protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020116 GCST90100601 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 40S ribosomal protein S3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 40s ribosomal protein S3 measurement http://www.ebi.ac.uk/efo/EFO_0020117 GCST90100602 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 40S ribosomal protein S7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 40s ribosomal protein S7 measurement http://www.ebi.ac.uk/efo/EFO_0020118 GCST90100603 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 40S ribosomal protein SA levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 40s ribosomal protein SA measurement http://www.ebi.ac.uk/efo/EFO_0020119 GCST90100604 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 6-phosphogluconate dehydrogenase, decarboxylating levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 6-phosphogluconate dehydrogenase, decarboxylating measurement http://www.ebi.ac.uk/efo/EFO_0020120 GCST90100605 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 60 kDa heat shock protein, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 60 kda heat shock protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020121 GCST90100606 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. 72 kDa type IV collagenase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 72 kda type IV collagenase measurement http://www.ebi.ac.uk/efo/EFO_0020122 GCST90100607 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90100608 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. A disintegrin and metalloproteinase with thrombospondin motifs 13 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90100609 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SLIT and NTRK-like protein 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 slit and ntrk-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020743 GCST90101557 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Small glutamine-rich tetratricopeptide repeat-containing protein alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 small glutamine-rich tetratricopeptide repeat-containing protein alpha measurement http://www.ebi.ac.uk/efo/EFO_0020744 GCST90101558 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Small nuclear ribonucleoprotein F levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 small nuclear ribonucleoprotein F measurement http://www.ebi.ac.uk/efo/EFO_0008288 GCST90101559 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Somatostatin-28 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 somatostatin-28 measurement http://www.ebi.ac.uk/efo/EFO_0020745 GCST90101560 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sonic hedgehog protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sonic hedgehog protein measurement http://www.ebi.ac.uk/efo/EFO_0020746 GCST90101561 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sorting nexin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sorting nexin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020747 GCST90101562 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SPARC levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90101563 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SPARC-like protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90101564 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Spectrin alpha chain, non-erythrocytic 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 spectrin alpha chain, non-erythrocytic 1 measurement http://www.ebi.ac.uk/efo/EFO_0020749 GCST90101565 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sphingosine kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sphingosine kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020750 GCST90101566 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Sphingosine kinase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sphingosine kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020751 GCST90101567 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Spondin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90101568 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stabilin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stabilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020752 GCST90101569 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stanniocalcin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stanniocalcin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020753 GCST90101570 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stem Cell Growth Factor-alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stem cell growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020754 GCST90101571 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stem Cell Growth Factor-beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stem Cell Growth Factor beta measurement http://www.ebi.ac.uk/efo/EFO_0008292 GCST90101572 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stress-induced-phosphoprotein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stress-induced-phosphoprotein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020755 GCST90101573 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet factor 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020644 GCST90101426 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet glycoprotein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 platelet glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008262 GCST90101427 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet glycoprotein Ib alpha chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet glycoprotein ib alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0020645 GCST90101428 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet glycoprotein VI levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 platelet glycoprotein VI measurement http://www.ebi.ac.uk/efo/EFO_0008263 GCST90101429 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet-activating factor acetylhydrolase IB subunit beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet-activating factor acetylhydrolase ib subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020646 GCST90101430 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet-activating factor acetylhydrolase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet-activating factor acetylhydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020647 GCST90101431 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet-derived growth factor C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet-derived growth factor c measurement http://www.ebi.ac.uk/efo/EFO_0020648 GCST90101432 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet-derived growth factor receptor beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90101433 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Resistin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90101501 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Reticulon-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 reticulon-4 measurement http://www.ebi.ac.uk/efo/EFO_0020704 GCST90101502 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Reticulon-4 receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90101503 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Retinoblastoma-associated protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 retinoblastoma-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0020706 GCST90101504 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Retinoic acid receptor responder protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 retinoic acid receptor responder protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008274 GCST90101505 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Retinol-binding protein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 retinol-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020707 GCST90101506 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. RGM domain family member B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 rgm domain family member b measurement http://www.ebi.ac.uk/efo/EFO_0020708 GCST90101507 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ribosomal protein S6 kinase alpha-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ribosomal protein s6 kinase alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020709 GCST90101508 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ribosomal protein S6 kinase alpha-5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ribosomal protein s6 kinase alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0020710 GCST90101509 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ribosome maturation protein SBDS levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ribosome maturation protein sbds measurement http://www.ebi.ac.uk/efo/EFO_0020711 GCST90101510 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. RNA-binding protein 39 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 rna-binding protein 39 measurement http://www.ebi.ac.uk/efo/EFO_0020712 GCST90101511 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Roundabout homolog 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 roundabout homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0020713 GCST90101512 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Roundabout homolog 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 roundabout homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0020714 GCST90101513 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. S-formylglutathione hydrolase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 S-formylglutathione hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0008275 GCST90101514 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. S-phase kinase-associated protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 s-phase kinase-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020715 GCST90101515 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Scavenger receptor class F member 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90101516 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Scavenger receptor class F member 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90101517 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stromal cell-derived factor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stromal cell-derived factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020756 GCST90101574 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stromelysin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stromelysin‐1 measurement http://www.ebi.ac.uk/efo/EFO_0010608 GCST90101575 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Stromelysin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 stromelysin‐2 measurement http://www.ebi.ac.uk/efo/EFO_0010621 GCST90101576 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. SUMO-conjugating enzyme UBC9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 sumo-conjugating enzyme UBC9 measurement http://www.ebi.ac.uk/efo/EFO_0020757 GCST90101577 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Superoxide dismutase [Cu-Zn] levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 superoxide dismutase [Cu-Zn] measurement http://www.ebi.ac.uk/efo/EFO_0020758 GCST90101578 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Superoxide dismutase [Mn], mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 superoxide dismutase [Mn], mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008294 GCST90101579 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Syntaxin-1A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 syntaxin-1a measurement http://www.ebi.ac.uk/efo/EFO_0020759 GCST90101580 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. T-cell surface glycoprotein CD4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 t-cell surface glycoprotein CD4 measurement http://www.ebi.ac.uk/efo/EFO_0020760 GCST90101581 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. T-lymphocyte activation antigen CD80 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 t-lymphocyte activation antigen CD80 measurement http://www.ebi.ac.uk/efo/EFO_0020761 GCST90101582 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. T-lymphocyte activation antigen CD86 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 t-lymphocyte activation antigen CD86 measurement http://www.ebi.ac.uk/efo/EFO_0020762 GCST90101583 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. T-lymphocyte surface antigen Ly-9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 T-lymphocyte surface antigen Ly-9 measurement http://www.ebi.ac.uk/efo/EFO_0008295 GCST90101584 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tartrate-resistant acid phosphatase type 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90101585 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. TATA-box-binding protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tata-box-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020764 GCST90101586 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Tenascin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90101587 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Teratocarcinoma-derived growth factor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90101588 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Testican-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 testican-1 measurement http://www.ebi.ac.uk/efo/EFO_0020765 GCST90101589 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Testican-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 testican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020766 GCST90101590 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. TGF-beta receptor type-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 tgf-beta receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020767 GCST90101591 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thioredoxin domain-containing protein 12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90101592 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thrombin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thrombin measurement http://www.ebi.ac.uk/efo/EFO_0020768 GCST90101593 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thrombopoietin Receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thrombopoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020769 GCST90101594 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thrombospondin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thrombospondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020770 GCST90101595 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thrombospondin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90101596 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thrombospondin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thrombospondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020771 GCST90101597 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Thymic stromal lymphopoietin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 thymic stromal lymphopoietin measurement http://www.ebi.ac.uk/efo/EFO_0020772 GCST90101598 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Scavenger receptor cysteine-rich type 1 protein M130 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 scavenger receptor cysteine-rich type 1 protein m130 measurement http://www.ebi.ac.uk/efo/EFO_0020717 GCST90101518 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Secreted frizzled-related protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 secreted frizzled-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020718 GCST90101519 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Secreted frizzled-related protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90101520 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Secretin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 secretin measurement http://www.ebi.ac.uk/efo/EFO_0020719 GCST90101521 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Seizure 6-like protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 seizure 6-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020720 GCST90101522 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Semaphorin-3A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90101523 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Semaphorin-3E levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90101524 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Semaphorin-6A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90101525 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Seprase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 seprase measurement http://www.ebi.ac.uk/efo/EFO_0020722 GCST90101526 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine protease 27 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 serine protease 27 measurement http://www.ebi.ac.uk/efo/EFO_0008280 GCST90101527 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine protease HTRA2, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine protease HTRA2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020723 GCST90101528 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase 16 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase 16 measurement http://www.ebi.ac.uk/efo/EFO_0020724 GCST90101529 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase 17B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 serine/threonine-protein kinase 17B measurement http://www.ebi.ac.uk/efo/EFO_0008281 GCST90101530 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase Chk1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90101531 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase Chk2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase CHK2 measurement http://www.ebi.ac.uk/efo/EFO_0020726 GCST90101532 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase MRCK beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase MRCK beta measurement http://www.ebi.ac.uk/efo/EFO_0020727 GCST90101533 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase PAK 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase PAK 3 measurement http://www.ebi.ac.uk/efo/EFO_0020728 GCST90101534 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase PAK 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase PAK 6 measurement http://www.ebi.ac.uk/efo/EFO_0020729 GCST90101535 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase PAK 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase PAK 7 measurement http://www.ebi.ac.uk/efo/EFO_0020730 GCST90101536 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase pim-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase PIM-1 measurement http://www.ebi.ac.uk/efo/EFO_0020731 GCST90101537 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase PLK1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase PLK1 measurement http://www.ebi.ac.uk/efo/EFO_0020732 GCST90101538 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase receptor R3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase receptor R3 measurement http://www.ebi.ac.uk/efo/EFO_0020733 GCST90101539 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serine/threonine-protein kinase TBK1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serine/threonine-protein kinase TBK1 measurement http://www.ebi.ac.uk/efo/EFO_0020734 GCST90101540 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serotransferrin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020735 GCST90101541 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Serum albumin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90101542 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibronectin Fragment 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 fibronectin fragment 3 measurement http://www.ebi.ac.uk/efo/EFO_0008131 GCST90101019 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibronectin Fragment 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 fibronectin fragment 4 measurement http://www.ebi.ac.uk/efo/EFO_0008132 GCST90101020 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibronectin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 fibronectin measurement http://www.ebi.ac.uk/efo/EFO_0008133 GCST90101021 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ficolin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90101022 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ficolin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 ficolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008135 GCST90101023 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ficolin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ficolin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020392 GCST90101024 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fms-related tyrosine kinase 3 ligand levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90101025 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Focal adhesion kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 focal adhesion kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020393 GCST90101026 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Follicle stimulating hormone levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90101027 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Follistatin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 follistatin measurement http://www.ebi.ac.uk/efo/EFO_0010614 GCST90101028 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Follistatin-related protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 follistatin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020394 GCST90101029 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fractalkine levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fractalkine measurement http://www.ebi.ac.uk/efo/EFO_0020395 GCST90101030 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. G2/mitotic-specific cyclin-B1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 g2/mitotic-specific cyclin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020396 GCST90101031 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Galactoside 3(4)-L-fucosyltransferase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 galactoside 34-L-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0008136 GCST90101032 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Galectin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 galectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020397 GCST90101033 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Galectin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90101034 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Galectin-3-binding protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 galectin-3-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010241 GCST90101035 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Galectin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 galectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020398 GCST90101036 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Galectin-8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 galectin-8 measurement http://www.ebi.ac.uk/efo/EFO_0020399 GCST90101037 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. GDNF family receptor alpha-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 gdnf family receptor alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020400 GCST90101038 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. GDNF family receptor alpha-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 GDNF family receptor alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0008138 GCST90101039 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. GDNF family receptor alpha-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 gdnf family receptor alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020401 GCST90101040 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Gelsolin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 gelsolin measurement http://www.ebi.ac.uk/efo/EFO_0020402 GCST90101041 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glia-derived nexin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glia-derived nexin measurement http://www.ebi.ac.uk/efo/EFO_0020403 GCST90101042 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glial fibrillary acidic protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90101043 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hepatocyte growth factor receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 hepatocyte growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0008153 GCST90101094 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hepatocyte growth factor-like protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90101095 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hepatoma-derived growth factor-related protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 hepatoma-derived growth factor-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020439 GCST90101096 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hepcidin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 hepcidin measurement http://www.ebi.ac.uk/efo/EFO_0020440 GCST90101097 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heterogeneous nuclear ribonucleoprotein A/B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heterogeneous nuclear ribonucleoprotein a/b measurement http://www.ebi.ac.uk/efo/EFO_0020441 GCST90101098 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heterogeneous nuclear ribonucleoprotein K levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heterogeneous nuclear ribonucleoprotein k measurement http://www.ebi.ac.uk/efo/EFO_0020442 GCST90101099 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heterogeneous nuclear ribonucleoprotein Q levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heterogeneous nuclear ribonucleoprotein q measurement http://www.ebi.ac.uk/efo/EFO_0020443 GCST90101100 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heterogeneous nuclear ribonucleoproteins A2/B1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heterogeneous nuclear ribonucleoproteins A2/B1 measurement http://www.ebi.ac.uk/efo/EFO_0020444 GCST90101101 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7a measurement http://www.ebi.ac.uk/efo/EFO_0020445 GCST90101102 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 high affinity cgmp-specific 3',5'-cyclic phosphodiesterase 9a measurement http://www.ebi.ac.uk/efo/EFO_0020446 GCST90101103 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. High affinity immunoglobulin gamma Fc receptor I levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 high affinity immunoglobulin gamma fc receptor i measurement http://www.ebi.ac.uk/efo/EFO_0020447 GCST90101104 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. High affinity nerve growth factor receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 high affinity nerve growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020448 GCST90101105 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. High mobility group protein B1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 high mobility group protein B1 measurement http://www.ebi.ac.uk/efo/EFO_0020449 GCST90101106 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histidine triad nucleotide-binding protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 histidine triad nucleotide-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020450 GCST90101107 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histidine-rich glycoprotein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 histidine-rich glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008155 GCST90101108 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histone acetyltransferase KAT6A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 histone acetyltransferase kat6a measurement http://www.ebi.ac.uk/efo/EFO_0020451 GCST90101109 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histone acetyltransferase type B catalytic subunit levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 histone acetyltransferase type b catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0020452 GCST90101110 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histone deacetylase 8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 histone deacetylase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020453 GCST90101111 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histone H1.2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90101112 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histone H2A.z levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 histone H2A.Z measurement http://www.ebi.ac.uk/efo/EFO_0020454 GCST90101113 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Histone-lysine N-methyltransferase EHMT2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 histone-lysine n-methyltransferase EHMT2 measurement http://www.ebi.ac.uk/efo/EFO_0020455 GCST90101114 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Homeobox protein NANOG levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 homeobox protein nanog measurement http://www.ebi.ac.uk/efo/EFO_0020456 GCST90101115 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Homeodomain-interacting protein kinase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 homeodomain-interacting protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020457 GCST90101116 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hsp90 co-chaperone Cdc37 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 hsp90 co-chaperone CDC37 measurement http://www.ebi.ac.uk/efo/EFO_0020458 GCST90101117 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Human Chorionic Gonadotropin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90101118 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Group 10 secretory phospholipase A2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 group 10 secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020423 GCST90101069 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Group IIE secretory phospholipase A2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 group IIe secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020424 GCST90101070 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Growth arrest-specific protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 growth arrest-specific protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020425 GCST90101071 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Growth hormone receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 growth hormone receptor measurement http://www.ebi.ac.uk/efo/EFO_0020426 GCST90101072 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Growth-regulated alpha protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST90101073 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Growth/differentiation factor 11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90101074 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Growth/differentiation factor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 growth/differentiation factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020428 GCST90101075 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Growth/differentiation factor 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 growth/differentiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020429 GCST90101076 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Growth/differentiation factor 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 growth/differentiation factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020430 GCST90101077 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. GTP-binding nuclear protein Ran levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 GTP-binding nuclear protein ran measurement http://www.ebi.ac.uk/efo/EFO_0020431 GCST90101078 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. GTPase KRas levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 GTPase kras measurement http://www.ebi.ac.uk/efo/EFO_0020432 GCST90101079 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Haptoglobin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 7 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90101080 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heat shock 70 kDa protein 1A/1B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heat shock 70 kda protein 1a/1b measurement http://www.ebi.ac.uk/efo/EFO_0020433 GCST90101081 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heat shock cognate 71 kDa protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heat shock cognate 71 kda protein measurement http://www.ebi.ac.uk/efo/EFO_0020434 GCST90101082 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heat shock protein HSP 90-alpha/beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heat shock protein hsp 90-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020435 GCST90101083 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heme oxygenase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heme oxygenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020436 GCST90101084 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hemoglobin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90101085 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hemojuvelin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 hemojuvelin measurement http://www.ebi.ac.uk/efo/EFO_0008148 GCST90101086 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hemopexin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90101087 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heparan-sulfate 6-O-sulfotransferase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heparan-sulfate 6-o-sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020437 GCST90101088 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heparin cofactor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 heparin cofactor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008150 GCST90101089 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Heparin-binding EGF-like growth factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 heparin-binding egf-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020438 GCST90101090 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hepatitis A virus cellular receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90101091 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hepatocyte growth factor activator levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 hepatocyte growth factor activator measurement http://www.ebi.ac.uk/efo/EFO_0008152 GCST90101092 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hepatocyte growth factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90101093 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glucagon levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90101044 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glucocorticoid receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glucocorticoid receptor measurement http://www.ebi.ac.uk/efo/EFO_0020405 GCST90101045 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glucokinase regulatory protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glucokinase regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0020406 GCST90101046 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glucose-6-phosphate isomerase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glucose-6-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020407 GCST90101047 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glutamate carboxypeptidase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90101048 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glutathione S-transferase A3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glutathione s-transferase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020409 GCST90101049 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glutathione S-transferase P levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90101050 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glyceraldehyde-3-phosphate dehydrogenase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glyceraldehyde-3-phosphate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0020411 GCST90101051 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glycogen synthase kinase-3 alpha/beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glycogen synthase kinase-3 alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020412 GCST90101052 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glycylpeptide N-tetradecanoyltransferase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glycylpeptide n-tetradecanoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020413 GCST90101053 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glypican-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glypican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020414 GCST90101054 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glypican-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 glypican-3 measurement http://www.ebi.ac.uk/efo/EFO_0020415 GCST90101055 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Glypican-5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 glypican-5 measurement http://www.ebi.ac.uk/efo/EFO_0008139 GCST90101056 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. gp41 C34 peptide, HIV levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 gp41 C34 peptide, HIV measurement http://www.ebi.ac.uk/efo/EFO_0008140 GCST90101057 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granulins levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90101058 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granulocyte colony-stimulating factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90101059 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granulocyte colony-stimulating factor receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 granulocyte colony-stimulating factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020416 GCST90101060 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granulocyte-macrophage colony-stimulating factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 granulocyte-macrophage colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0020417 GCST90101061 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granulysin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90101062 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granzyme A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90101063 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granzyme B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 granzyme b measurement http://www.ebi.ac.uk/efo/EFO_0020418 GCST90101064 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Granzyme H levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 granzyme h measurement http://www.ebi.ac.uk/efo/EFO_0020419 GCST90101065 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. GRB2-related adapter protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90101066 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Gremlin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 gremlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020421 GCST90101067 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Gro-beta/gamma levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 gro-beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0020422 GCST90101068 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Hyaluronan and proteoglycan link protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 hyaluronan and proteoglycan link protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020459 GCST90101119 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. ICOS ligand levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90101120 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Iduronate 2-sulfatase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 iduronate 2-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020461 GCST90101121 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Immunoglobulin alpha Fc receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 immunoglobulin alpha fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0020462 GCST90101122 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Immunoglobulin D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 immunoglobulin D measurement http://www.ebi.ac.uk/efo/EFO_0020463 GCST90101123 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Immunoglobulin E levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 immunoglobulin E measurement http://www.ebi.ac.uk/efo/EFO_0020464 GCST90101124 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Immunoglobulin G levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 immunoglobulin G measurement http://www.ebi.ac.uk/efo/EFO_0020465 GCST90101125 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Immunoglobulin M levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 immunoglobulin M measurement http://www.ebi.ac.uk/efo/EFO_0020466 GCST90101126 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Importin subunit alpha-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 importin subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020467 GCST90101127 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Importin subunit beta-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 importin subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020468 GCST90101128 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Inhibin beta A chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 inhibin beta A chain measurement http://www.ebi.ac.uk/efo/EFO_0020469 GCST90101129 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Inhibin beta A chain:Inhibin beta B chain heterodimer levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 inhibin beta A chain:inhibin beta B chain heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020470 GCST90101130 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Inhibitor of growth protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 inhibitor of growth protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020471 GCST90101131 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Inorganic pyrophosphatase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 inorganic pyrophosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008157 GCST90101132 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Inosine-5'-monophosphate dehydrogenase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 inosine-5'-monophosphate dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008158 GCST90101133 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Inosine-5'-monophosphate dehydrogenase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 inosine-5'-monophosphate dehydrogenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008159 GCST90101134 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90101135 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 insulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008160 GCST90101136 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-degrading enzyme levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin-degrading enzyme measurement http://www.ebi.ac.uk/efo/EFO_0020472 GCST90101137 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor 1 receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin-like growth factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020473 GCST90101138 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor I levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST90101139 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor-binding protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90101140 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor-binding protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90101141 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor-binding protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 IGFBP-3 measurement http://www.ebi.ac.uk/efo/EFO_0004626 GCST90101142 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Insulin-like growth factor-binding protein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 insulin-like growth factor-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020476 GCST90101143 Genome-wide genotyping array 2022-01-18 34536413 Daya M 2021-09-15 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34536413 Multi-ethnic genome-wide and HLA association study of total serum IgE. IgE levels 5,008 African American individuals, 12,908 European ancestry individuals, 3,985 Hispanic individuals NA Affymetrix, Illumina [NR] (imputed) 6 serum IgE measurement http://www.ebi.ac.uk/efo/EFO_0004579 GCST90091054 Genome-wide genotyping array, Genome-wide sequencing 2022-02-28 34941638 Avasthi KK 2021-12-08 Pediatr Rep www.ncbi.nlm.nih.gov/pubmed/34941638 Identification of Novel Genomic Variations in Susceptibility to Nonsyndromic Cleft Lip and Palate Patients. Nonsyndromic cleft lip with or without cleft palate 86 Indian ancestry cases, 10 Indian ancestry controls NA Affymetrix [810906] 14 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST90095043 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cell adhesion molecule-related/down-regulated by oncogenes levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 cell adhesion molecule-related/down-regulated by oncogenes measurement http://www.ebi.ac.uk/efo/EFO_0008079 GCST90100819 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cell surface glycoprotein CD200 receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cell surface glycoprotein CD200 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020253 GCST90100820 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cerebral dopamine neurotrophic factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90100821 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. cGMP-dependent 3',5'-cyclic phosphodiesterase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cGMP-specific 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0008081 GCST90100822 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. cGMP-inhibited 3',5'-cyclic phosphodiesterase A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cGMP-inhibited 3',5'-cyclic phosphodiesterase A measurement http://www.ebi.ac.uk/efo/EFO_0020255 GCST90100823 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. cGMP-specific 3',5'-cyclic phosphodiesterase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 cGMP-specific 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0008081 GCST90100824 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Chitotriosidase-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90100825 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Chloride intracellular channel protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 chloride intracellular channel protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020256 GCST90100826 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Chordin-like protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 chordin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020257 GCST90100827 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Chromobox protein homolog 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 chromobox protein homolog 5 measurement http://www.ebi.ac.uk/efo/EFO_0020258 GCST90100828 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Chymase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 chymase measurement http://www.ebi.ac.uk/efo/EFO_0020259 GCST90100829 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ciliary Neurotrophic Factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ciliary neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020260 GCST90100830 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ciliary neurotrophic factor receptor subunit alpha levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ciliary neurotrophic factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020261 GCST90100831 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ck-beta-8-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 Ck-beta-8-1 measurement http://www.ebi.ac.uk/efo/EFO_0008085 GCST90100832 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Clusterin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007655 GCST90100833 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. CMRF35-like molecule 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90100834 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coactosin-like protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 coactosin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020262 GCST90100835 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coagulation factor IX levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 coagulation factor IX measurement http://www.ebi.ac.uk/efo/EFO_0020263 GCST90100836 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coagulation factor IXab levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 coagulation factor IXAB measurement http://www.ebi.ac.uk/efo/EFO_0020264 GCST90100837 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coagulation Factor V levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST90100838 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coagulation Factor VII levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST90100839 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coagulation Factor X levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 coagulation factor X measurement http://www.ebi.ac.uk/efo/EFO_0020265 GCST90100840 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coagulation factor Xa levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 coagulation factor XA measurement http://www.ebi.ac.uk/efo/EFO_0020266 GCST90100841 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coagulation Factor XI levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 factor XI measurement http://www.ebi.ac.uk/efo/EFO_0004694 GCST90100842 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cofilin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cofilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020267 GCST90100843 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cystatin-M levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90100894 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cystatin-S levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cystatin-S measurement http://www.ebi.ac.uk/efo/EFO_0020300 GCST90100895 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cystatin-SA levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 cystatin-SA measurement http://www.ebi.ac.uk/efo/EFO_0008105 GCST90100896 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cystatin-SN levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 cystatin-SN measurement http://www.ebi.ac.uk/efo/EFO_0008106 GCST90100897 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cysteine-rich secretory protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cysteine-rich secretory protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020301 GCST90100898 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytochrome c levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytochrome C measurement http://www.ebi.ac.uk/efo/EFO_0020302 GCST90100899 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytochrome P450 3A4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytochrome p450 3a4 measurement http://www.ebi.ac.uk/efo/EFO_0020303 GCST90100900 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytokine receptor common subunit gamma levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytokine receptor common subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0020304 GCST90100901 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytokine receptor-like factor 1:Cardiotrophin-like cytokine factor 1 Complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytokine receptor-like factor 1:cardiotrophin-like cytokine factor 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020305 GCST90100902 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytokine receptor-like factor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytokine receptor-like factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020306 GCST90100903 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytoplasmic protein NCK1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytoplasmic protein NCK1 measurement http://www.ebi.ac.uk/efo/EFO_0020307 GCST90100904 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytoplasmic tyrosine-protein kinase BMX levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytoplasmic tyrosine-protein kinase BMX measurement http://www.ebi.ac.uk/efo/EFO_0020308 GCST90100905 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytoskeleton-associated protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytoskeleton-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020309 GCST90100906 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytosolic non-specific dipeptidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytosolic non-specific dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020310 GCST90100907 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytotoxic and regulatory T-cell molecule levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytotoxic and regulatory t-cell molecule measurement http://www.ebi.ac.uk/efo/EFO_0020311 GCST90100908 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cytotoxic T-lymphocyte protein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cytotoxic t-lymphocyte protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020312 GCST90100909 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. D-dimer levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 D dimer measurement http://www.ebi.ac.uk/efo/EFO_0004507 GCST90100910 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. dCTP pyrophosphatase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 DCTP pyrophosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020314 GCST90100911 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Death-associated protein kinase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 death-associated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008107 GCST90100912 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Decorin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 decorin measurement http://www.ebi.ac.uk/efo/EFO_0020315 GCST90100913 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Delta-like protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90100914 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Delta-like protein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 delta-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020317 GCST90100915 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dentin matrix acidic phosphoprotein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dentin matrix acidic phosphoprotein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020318 GCST90100916 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dermatopontin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90100917 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Desert hedgehog protein N-product levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 desert hedgehog protein n-product measurement http://www.ebi.ac.uk/efo/EFO_0020319 GCST90100918 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement factor D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90100869 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement factor H levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 5 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90100870 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement factor H-related protein 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90100871 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement factor I levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 complement factor I measurement http://www.ebi.ac.uk/efo/EFO_0008099 GCST90100872 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Connective tissue growth factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 connective tissue growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020284 GCST90100873 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Connective tissue-activating peptide III levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 connective tissue-activating peptide III measurement http://www.ebi.ac.uk/efo/EFO_0020285 GCST90100874 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Contactin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 contactin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020286 GCST90100875 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Contactin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90100876 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Contactin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 contactin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020287 GCST90100877 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Contactin-5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 contactin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008101 GCST90100878 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Copine-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90100879 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Corticosteroid-binding globulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 corticosteroid-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0020288 GCST90100880 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Corticotropin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 corticotropin measurement http://www.ebi.ac.uk/efo/EFO_0020289 GCST90100881 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Creatine kinase B-type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 creatine kinase b-type measurement http://www.ebi.ac.uk/efo/EFO_0020290 GCST90100882 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Creatine kinase M-type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 creatine kinase m-type measurement http://www.ebi.ac.uk/efo/EFO_0020291 GCST90100883 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Creatine kinase M-type:Creatine kinase B-type heterodimer levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 creatine kinase m-type:creatine kinase b-type heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020292 GCST90100884 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cryptic protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cryptic protein measurement http://www.ebi.ac.uk/efo/EFO_0020293 GCST90100885 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cyclin-dependent kinase 1:G2/mitotic-specific cyclin-B1 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cyclin-dependent kinase 1:g2/mitotic-specific cyclin-B1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020294 GCST90100886 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cyclin-dependent kinase 2:Cyclin-A2 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cyclin-dependent kinase 2:cyclin-A2 complex measurement http://www.ebi.ac.uk/efo/EFO_0020295 GCST90100887 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cyclin-dependent kinase 5:Cyclin-dependent kinase 5 activator 1 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cyclin-dependent kinase 5:cyclin-dependent kinase 5 activator 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020296 GCST90100888 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cyclin-dependent kinase 8:Cyclin-C complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cyclin-dependent kinase 8:cyclin-c complex measurement http://www.ebi.ac.uk/efo/EFO_0020297 GCST90100889 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cyclin-dependent kinase inhibitor 1B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 cyclin-dependent kinase inhibitor 1b measurement http://www.ebi.ac.uk/efo/EFO_0020298 GCST90100890 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cystatin-C levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90100891 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cystatin-D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90100892 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Cystatin-F levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90100893 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Coiled-coil domain-containing protein 80 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 coiled-coil domain-containing protein 80 measurement http://www.ebi.ac.uk/efo/EFO_0020268 GCST90100844 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Collagen alpha-1(VIII) chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 collagen alpha-1(VIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020269 GCST90100845 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Collagen alpha-1(XXIII) chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 collagen alpha-1(XXIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020270 GCST90100846 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Collagenase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 collagenase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020271 GCST90100847 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Collectin-11 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90100848 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Collectin-12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90100849 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. COMM domain-containing protein 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 COMM domain-containing protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020273 GCST90100850 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C1q subcomponent levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90100851 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C1r subcomponent levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 complement C1r subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008090 GCST90100852 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C1s subcomponent levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 complement C1s subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008091 GCST90100853 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement C2 measurement http://www.ebi.ac.uk/efo/EFO_0020274 GCST90100854 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90100855 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C3b levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement C3B measurement http://www.ebi.ac.uk/efo/EFO_0020275 GCST90100856 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C3b, inactivated levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement C3B, inactivated measurement http://www.ebi.ac.uk/efo/EFO_0020276 GCST90100857 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C3d fragment levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement C3D fragment measurement http://www.ebi.ac.uk/efo/EFO_0020277 GCST90100858 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST90100859 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement C5 measurement http://www.ebi.ac.uk/efo/EFO_0020278 GCST90100860 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement C5b-C6 complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement C5B-C6 complex measurement http://www.ebi.ac.uk/efo/EFO_0020279 GCST90100861 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement component 1 Q subcomponent-binding protein, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement component 1 q subcomponent-binding protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020280 GCST90100862 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement component C6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement component C6 measurement http://www.ebi.ac.uk/efo/EFO_0020281 GCST90100863 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement component C7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 4 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90100864 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement component C8 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 complement component C8 measurement http://www.ebi.ac.uk/efo/EFO_0008094 GCST90100865 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement component C9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90100866 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement decay-accelerating factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 complement decay-accelerating factor measurement http://www.ebi.ac.uk/efo/EFO_0008095 GCST90100867 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Complement factor B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 complement factor B measurement http://www.ebi.ac.uk/efo/EFO_0008096 GCST90100868 Genome-wide genotyping array 2022-02-16 34553764 Little A 2021-09-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34553764 Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative. Platelet count 14,392 African American individuals, 13,985 Hispanic or Latin American individuals, 32,129 European ancestry individuals, 681 East Asian ancestry individuals, 13 individuals 10,664 individuals, 10,694 African American individuals, 7,287 Hispanic or Latin American individuals, 7,857 African ancestry individuals NR [NR] 19 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90094627 Genome-wide sequencing 2022-02-16 34553764 Little A 2021-09-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34553764 Whole genome sequence analysis of platelet traits in the NHLBI trans-omics for precision medicine initiative. Mean platelet volume 7,440 African American individuals, 5,466 Hispanic or Latin American individuals, 10,120 European ancestry individuals, 447 East Asian ancestry individuals, 12 individuals 7,857 African ancestry individuals NR [NR] 5 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90094628 Genome-wide sequencing 2022-01-24 33637690 He L 2021-02-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33637690 Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer's disease. Alzheimer's disease (age of onset) 10,216 European ancestry individuals 9,261 European ancestry individuals NR [110450] 4 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST90093287 Exome-wide sequencing 2022-01-24 33637690 He L 2021-02-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33637690 Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer's disease. Alzheimer's disease (age of onset) (adjusted for APOE e4 carrier status) 10,216 European ancestry individuals 9,261 European ancestry individuals NR [110450] 3 APOE carrier status, age of onset of Alzheimer disease http://www.ebi.ac.uk/efo/EFO_0007659, http://purl.obolibrary.org/obo/OBA_2001000 GCST90093288 Exome-wide sequencing 2022-01-24 33637690 He L 2021-02-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33637690 Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer's disease. Alzheimer's disease (age of onset) in APOE e4 non-carriers 7,185 European ancestry individuals 5,416 European ancestry individuals NR [98334] 9 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST90093289 Exome-wide sequencing 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Apolipoprotein A1 levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 85 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90092808 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of apolipoprotein B to apolipoprotein A1 levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 78 apolipoprotein A 1 measurement, apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004614, http://www.ebi.ac.uk/efo/EFO_0004615 GCST90092810 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total cholines levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 69 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90092812 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of docosahexaenoic acid to total fatty acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 27 docosahexaenoic acid measurement, fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0007761, http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092817 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 111 cholesteryl ester measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092823 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 91 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092824 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 94 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092825 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of HDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 73 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092826 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 89 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092827 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Average diameter for HDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 115 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90092828 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 74 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092829 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 73 total cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092831 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 97 cholesterol:total lipids ratio, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092832 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 70 cholesteryl ester measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092833 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 83 cholesteryl esters:total lipids ratio, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020944, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092834 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 74 free cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092835 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 59 free cholesterol:total lipids ratio, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020945, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092836 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 71 lipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092837 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of IDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 59 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092838 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 73 phospholipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092839 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 53 phospholipids:total lipids ratio, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020946, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092840 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 87 triglyceride measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092841 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in IDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 100 triglycerides:total lipids ratio, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90092842 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 129 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092844 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 107 cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092845 Genome-wide genotyping array 2022-02-23 34716350 Lin WY 2021-10-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34716350 Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Acute myeloid leukemia (all cytogenetic sub-types) 3,041 European ancestry cases, 6,760 European ancestry controls 977 European ancestry cases, 3,728 European ancestry controls Affymetrix, Illumina [6661818] (imputed) 2 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST90094652 Genome-wide genotyping array 2022-02-23 34716350 Lin WY 2021-10-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34716350 Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Acute myeloid leukemia (normal cytogenetics) 3,041 European ancestry cases, 6,760 European ancestry controls 977 European ancestry cases, 3,728 European ancestry controls Affymetrix, Illumina [6496414] (imputed) 2 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST90094653 Genome-wide genotyping array 2022-04-06 35048876 Kalman JL 2021-12-01 Br J Psychiatry www.ncbi.nlm.nih.gov/pubmed/35048876 Characterisation of age and polarity at onset in bipolar disorder. Bipolar disorder (age of onset) 12,977 European ancestry individuals 2,237 European and unknown ancestry individuals NR [7576712] (imputed) 0 age of onset of bipolar disorder http://purl.obolibrary.org/obo/OBA_2001019 GCST90101734 Genome-wide genotyping array 2022-04-06 35048876 Kalman JL 2021-12-01 Br J Psychiatry www.ncbi.nlm.nih.gov/pubmed/35048876 Characterisation of age and polarity at onset in bipolar disorder. Polarity at onset of bipolar disorder (depression-first vs mania-first/mixed) 3,885 European ancestry cases, 2,888 European ancestry controls 2,237 European and unknown ancestry individuals NR [7586624] (imputed) 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90101735 Genome-wide genotyping array 2022-05-12 35162374 Yang CC 2022-01-26 Int J Environ Res Public Health www.ncbi.nlm.nih.gov/pubmed/35162374 Single Nucleotide Polymorphism of TWIST2 May Be a Modifier for the Association between High-Density Lipoprotein Cholesterol and Blood Lead (Pb) Level. Lead levels in blood 511 Han Chinese ancestry individuals NA Affymetrix [714431] 0 blood lead measurement http://www.ebi.ac.uk/efo/EFO_0007040 GCST90102512 Genome-wide genotyping array 2022-03-16 34214102 Sarnowski C 2021-07-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/34214102 Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Hand grip strength 13,552 European, African American or Afro-Caribbean, Hispanic or Latin American, Asian, Native American, Other ancestry individuals NA NR [638486] 5 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90095048 Genome-wide sequencing 2022-03-16 34214102 Sarnowski C 2021-07-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/34214102 Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Hand grip strength 4878 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Native American ancestry, Other ancestry men NA NR [638486] 3 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90095049 Genome-wide sequencing 2022-03-16 34214102 Sarnowski C 2021-07-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/34214102 Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Hand grip strength 8674 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Native American ancestry, Other ancestry women NA NR [638486] 5 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90095050 Genome-wide sequencing 2022-03-16 34214102 Sarnowski C 2021-07-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/34214102 Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Hand grip strength 3145 African American or Afro-Caribbean individuals NA NR [638486] 5 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90095051 Genome-wide sequencing 2022-03-16 34214102 Sarnowski C 2021-07-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/34214102 Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Hand grip strength 987 African American or Afro-Caribbean men NA NR [638486] 3 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90095052 Genome-wide sequencing 2022-03-07 34214102 Sarnowski C 2021-07-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/34214102 Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program. Hand grip strength 2158 African American or Afro-Caribbean women NA NR [638486] 4 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90095053 Genome-wide sequencing 2022-04-11 35347114 Harder A 2022-03-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35347114 Genetics of age-at-onset in major depression. Depression (age of onset) 94,154 European ancestry individuals NA Affymetrix [NR] (imputed) 0 unipolar depression, age at onset http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90101808 Genome-wide genotyping array 2022-05-12 35154085 Connell WT 2022-01-27 Front Immunol www.ncbi.nlm.nih.gov/pubmed/35154085 Genome-Wide Association Study of Ustekinumab Response in Psoriasis. Response to ustekinumab in psoriasis (improvement) 310 European ancestry individuals 129 European ancestry individuals Illumina [6799417] (imputed) 1 response to ustekinumab http://www.ebi.ac.uk/efo/EFO_0020986 GCST90102543 Genome-wide genotyping array 2022-05-12 35154085 Connell WT 2022-01-27 Front Immunol www.ncbi.nlm.nih.gov/pubmed/35154085 Genome-Wide Association Study of Ustekinumab Response in Psoriasis. Response to ustekinumab in psoriasis (improvement) 439 European ancestry individuals NA Illumina [NR] (imputed) 2 response to ustekinumab http://www.ebi.ac.uk/efo/EFO_0020986 GCST90102544 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin T levels 18,590 European ancestry individuals, 3,806 African American individuals, 774 Chinese ancestry individuals, 1,446 Hispanics ancestry individuals NA Affymetrix, Illumina [10661418] (imputed) 14 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90095172 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin I concentration 12,730 European ancestry individuals, 1,606 African American individuals NA Affymetrix, Illumina [6937320] (imputed) 3 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST90095173 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin T levels 18,590 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 36 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90095174 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin I concentration 12,730 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 18 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST90095175 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin T levels 3,806 African American individuals NA Affymetrix, Illumina [NR] (imputed) 50 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90095176 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin I concentration 1,606 African American individuals NA Affymetrix, Illumina [NR] (imputed) 66 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST90095177 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin T levels 774 Chinese ancestry individuals NA Affymetrix [NR] (imputed) 11 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90095178 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin T levels 1,446 Hispanics ancestry individuals NA Affymetrix [NR] (imputed) 4 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90095179 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin T levels (MTAG) 18,590 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 19 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90095180 Genome-wide genotyping array 2022-03-10 34732054 Yang Y 2021-11-04 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34732054 Identification of Functional Genetic Determinants of Cardiac Troponin T and I in a Multiethnic Population and Causal Associations With Atrial Fibrillation. High-sensitivity cardiac troponin I concentration (MTAG) 12,730 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 19 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST90095181 Genome-wide genotyping array 2022-05-13 35151124 Bae JH 2022-01-29 Clin Nutr www.ncbi.nlm.nih.gov/pubmed/35151124 Effect of dietary calcium on the gender-specific association between polymorphisms in the PTPRD locus and osteoporosis. Osteoporosis 8,842 Korean ancestry individuals NA NR [352228] 1 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90102600 Genome-wide genotyping array 2021-12-02 34782693 Yamada M 2021-11-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34782693 Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. Lung function (forced expiratory volume in 1 second) 14,061 Japanese ancestry individuals 5,661 Japanese ancestry individuals Affymetrix [8587571] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90044841 Genome-wide genotyping array 2021-12-02 34782693 Yamada M 2021-11-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34782693 Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. Lung function (FEV1/FVC) 14,061 Japanese ancestry individuals 5,661 Japanese ancestry individuals Affymetrix [8587571] (imputed) 2 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90044842 Genome-wide genotyping array 2021-12-02 34782693 Yamada M 2021-11-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34782693 Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. Exhaled nitric oxide levels 14,061 Japanese ancestry individuals 5,661 Japanese ancestry individuals Affymetrix [8587571] (imputed) 2 nitric oxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0005536 GCST90044843 Genome-wide genotyping array 2021-12-02 34782693 Yamada M 2021-11-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34782693 Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. Lung function (forced expiratory volume in 1 second) 5,661 Japanese ancestry individuals NA Affymetrix [8595665] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90044844 Genome-wide genotyping array 2021-12-02 34782693 Yamada M 2021-11-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34782693 Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. Lung function (FEV1/FVC) 5,661 Japanese ancestry individuals NA Affymetrix [8595665] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90044845 Genome-wide genotyping array 2021-12-02 34782693 Yamada M 2021-11-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34782693 Genetic loci for lung function in Japanese adults with adjustment for exhaled nitric oxide levels as airway inflammation indicator. Exhaled nitric oxide levels 5,661 Japanese ancestry individuals NA Affymetrix [8595665] (imputed) 0 nitric oxide exhalation measurement http://www.ebi.ac.uk/efo/EFO_0005536 GCST90044846 Genome-wide genotyping array 2022-03-09 34758156 Liu W 2021-11-10 Mol Carcinog www.ncbi.nlm.nih.gov/pubmed/34758156 Colorectal cancer risk susceptibility loci in a Swedish population. Colorectal cancer 2,663 cases, 1,642 controls NA Illumina [342359] 2 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90095126 Genome-wide genotyping array 2022-03-09 34758156 Liu W 2021-11-10 Mol Carcinog www.ncbi.nlm.nih.gov/pubmed/34758156 Colorectal cancer risk susceptibility loci in a Swedish population. Familial colorectal cancer 2,663 cases, 1,642 controls NA Illumina [342359] 6 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90095127 Genome-wide genotyping array 2022-03-09 34758156 Liu W 2021-11-10 Mol Carcinog www.ncbi.nlm.nih.gov/pubmed/34758156 Colorectal cancer risk susceptibility loci in a Swedish population. Non-familial colorectal cancer 2,663 cases, 1,642 controls NA Illumina [342359] 2 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90095128 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fusobacteriaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032405 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Fusobacterium A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032406 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. GCA-900066135 sp900066135 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032407 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. GCA-900066755 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032412 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Gemmatimonadaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032415 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Geobacteraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032416 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Geobacter C abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032417 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Gillisia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032418 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Gluconobacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032419 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Dialister sp000434475 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032345 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Dokdonella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032346 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Dorea phocaeense abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032347 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Dorea abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032348 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. DTU024 sp002411105 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032349 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Dysgonomonadaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032350 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eisenbergiella sp900066775 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032351 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Elusimicrobiaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032352 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Elusimicrobia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032353 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Elusimicrobiota abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 8 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032354 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Emergencia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032355 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Endozoicomonadaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032356 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enorma massiliensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032357 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Ensifer abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032358 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enterobacteriaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032359 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enterococcaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032360 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enterococcus A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032361 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enterococcus B abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032362 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enterococcus faecalis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032363 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enterococcus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032364 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Enteroscipio abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032365 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. ER4 sp002437735 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032366 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Eremiobacterota abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032367 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Erysipelatoclostridiaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032368 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Escherichia flexneri abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032369 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Gordonibacter pamelaeae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032420 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Gordonibacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032421 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Gramella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032422 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Haemophilus D sp001679485 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032423 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Halarcobacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032424 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Halomonadaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032425 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Haloplasmatales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032426 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Helicobacter abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032427 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Herbidospora abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032428 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Herbinix abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032429 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Holdemania massiliensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032430 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Holdemania sp900120005 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032431 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Holdemania abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032432 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Hungatella sp900155545 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032433 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Hydrogenophaga abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032434 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Hyphomonas abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032435 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Intestinimonas massiliensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032436 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Jiangellaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032437 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Johnsonella ignava abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032438 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. K10 sp001941205 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032439 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. K10 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032440 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Kandleria vitulina abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032441 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Kineothrix abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032442 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. KLE1615 sp900066985 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032443 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. KLE1615 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032444 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Massiliomicrobiota abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032470 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Megamonas funiformis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032471 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Megamonas abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032472 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Megasphaera elsdenii abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032473 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Megasphaera sp900066485 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032474 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Megasphaera abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032475 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Merdibacter massiliensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032476 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Methanobacterium B abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032477 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Methanobrevibacter B abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032478 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Microvirga abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032479 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Monoglobaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032480 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Monoglobus pectinilyticus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032481 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Monoglobus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032482 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Morganella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032483 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Mycobacteriaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032484 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Mycoplasmataceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032485 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Mycoplasmatales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032486 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Mycoplasmoidaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032487 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Negativibacillus massiliensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032488 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Negativibacillus sp000435195 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032489 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Negativibacillus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032490 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. NK4A144 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032491 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Odoribacter laneus abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032492 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Olsenella C abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032493 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Omnitrophota abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032494 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Klebsiella A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032445 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Klebsiella pneumoniae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032446 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Klebsiella abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032447 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. koll11 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032448 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lachnoanaerobaculum saburreum abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032449 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lachnospiraceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032450 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lachnospirales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032451 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lachnospira rogosae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032452 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lachnospira sp000437735 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032453 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lactobacillus B ruminis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032454 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lactobacillus B salivarius abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032455 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lactobacillus B abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032456 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lactococcus lactis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032457 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lawsonibacter sp000492175 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032458 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lawsonibacter sp002161175 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032459 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lawsonibacter sp900066645 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032460 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Leclercia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032461 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Lentimicrobiaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032462 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Leptospirae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032463 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Leptospirales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032464 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Leuconostoc mesenteroides abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032465 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Leuconostoc abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032466 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Magnetospirillum A abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032467 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Marinilabiliaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032468 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Massiliomicrobiota sp002160815 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032469 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Paceibacteria abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032495 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Paenibacillales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032496 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Paenibacillus J abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032497 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Pandoraea abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032498 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Parabacteroides johnsonii abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032499 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Parabacteroides sp000436495 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032500 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Parabacteroides abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032501 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Parachlamydiales abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032502 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Paraglaciecola abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032503 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Paramuribaculum sp001689565 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032504 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Pararhizobium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032505 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Pauljensenia sp000411415 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032506 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Peptococcia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032507 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Phascolarctobacterium sp003150755 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032508 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Phocea massiliensis abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032509 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Phocea abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032510 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Photobacterium abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032511 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Planococcaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032512 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Poseidoniaceae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032513 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella bivia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032514 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotella buccae abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032515 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotellamassilia sp000437675 abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032516 Genome-wide genotyping array 2022-02-24 35115689 Qin Y 2022-02-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35115689 Combined effects of host genetics and diet on human gut microbiota and incident disease in a single population cohort. Prevotellamassilia abundance in stool 5,959 Finnish ancestry individuals NA Illumina [7980478] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90032517 Genome-wide genotyping array 2022-02-23 34719679 Hu SH 2021-10-31 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34719679 Discovery of new genetic loci for male sexual orientation in Han population. Male sexual orientation 521 Han Chinese ancestry homosexual men, 1,270 Han Chinese ancestry heterosexual men 957 Han Chinese ancestry homosexual men, 2,043 Han Chinese ancestry heterosexual men Illumina [724550] (imputed) 2 male homosexuality http://www.ebi.ac.uk/efo/EFO_0008486 GCST90094930 Genome-wide genotyping array 2022-02-23 34719679 Hu SH 2021-10-31 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34719679 Discovery of new genetic loci for male sexual orientation in Han population. Male sexual orientation 188,825 European ancestry individuals, 4,791 Han Chinese ancestry individuals NA Illumina [NR] (imputed) 2 male homosexuality http://www.ebi.ac.uk/efo/EFO_0008486 GCST90094931 Genome-wide genotyping array 2022-02-23 34719679 Hu SH 2021-10-31 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34719679 Discovery of new genetic loci for male sexual orientation in Han population. Sexual orientation 408,995 European ancestry individuals, 4,791 Han Chinese ancestry individuals NA Illumina [NR] (imputed) 1 homosexuality http://www.ebi.ac.uk/efo/EFO_0008485 GCST90094932 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Nicotinamide phosphoribosyltransferase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 nicotinamide phosphoribosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0020607 GCST90101368 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Nidogen-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 nidogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008249 GCST90101369 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Nidogen-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90101370 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NKG2-D type II integral membrane protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 NKG2-D type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0008250 GCST90101371 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NKG2D ligand 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 NKG2-D ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020609 GCST90101372 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NKG2D ligand 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 NKG2-D ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0020610 GCST90101373 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NKG2D ligand 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 NKG2-D ligand 3 measurement http://www.ebi.ac.uk/efo/EFO_0020611 GCST90101374 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Non-receptor tyrosine-protein kinase TYK2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 non-receptor tyrosine-protein kinase TYK2 measurement http://www.ebi.ac.uk/efo/EFO_0008251 GCST90101375 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet-derived growth factor subunit A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet-derived growth factor subunitAmeasurement http://www.ebi.ac.uk/efo/EFO_0020649 GCST90101434 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet-derived growth factor subunit B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet-derived growth factor subunit b measurement http://www.ebi.ac.uk/efo/EFO_0020650 GCST90101435 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pleiotrophin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pleiotrophin measurement http://www.ebi.ac.uk/efo/EFO_0020651 GCST90101436 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Plexin-C1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 plexin-C1 measurement http://www.ebi.ac.uk/efo/EFO_0008266 GCST90101437 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Polymeric immunoglobulin receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90101438 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Prefoldin subunit 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 prefoldin subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0020652 GCST90101439 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Probable G-protein coupled receptor 114 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 probable g-protein coupled receptor 114 measurement http://www.ebi.ac.uk/efo/EFO_0020653 GCST90101440 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Programmed cell death 1 ligand 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90101441 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Programmed cell death 1 ligand 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 programmed cell death 1 ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0008268 GCST90101442 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Prokineticin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 prokineticin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020655 GCST90101443 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Prolactin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 prolactin measurement http://www.ebi.ac.uk/efo/EFO_0007003 GCST90101444 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Prolactin receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 prolactin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020656 GCST90101445 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proliferating cell nuclear antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proliferating cell nuclear antigen measurement http://www.ebi.ac.uk/efo/EFO_0020657 GCST90101446 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proliferation-associated protein 2G4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proliferation-associated protein 2g4 measurement http://www.ebi.ac.uk/efo/EFO_0020658 GCST90101447 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Properdin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 properdin measurement http://www.ebi.ac.uk/efo/EFO_0008269 GCST90101448 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proprotein convertase subtilisin/kexin type 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90101449 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proprotein convertase subtilisin/kexin type 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90101450 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Prostaglandin G/H synthase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 prostaglandin g/h synthase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020659 GCST90101451 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Prostate-specific antigen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 prostate-specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0020660 GCST90101452 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proteasome activator complex subunit 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90101453 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proteasome activator complex subunit 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proteasome activator complex subunit 3 measurement http://www.ebi.ac.uk/efo/EFO_0020662 GCST90101454 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proteasome subunit alpha type-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proteasome subunit alpha type-1 measurement http://www.ebi.ac.uk/efo/EFO_0020663 GCST90101455 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proteasome subunit alpha type-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proteasome subunit alpha type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020664 GCST90101456 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proteasome subunit alpha type-6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proteasome subunit alpha type-6 measurement http://www.ebi.ac.uk/efo/EFO_0020665 GCST90101457 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein 4.1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein 4.1 measurement http://www.ebi.ac.uk/efo/EFO_0020666 GCST90101458 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein amnionless levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein amnionless measurement http://www.ebi.ac.uk/efo/EFO_0020667 GCST90101459 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein disulfide-isomerase A3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein disulfide-isomerase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020668 GCST90101460 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein disulfide-isomerase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein disulfide-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020669 GCST90101461 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein DJ-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein dj-1 measurement http://www.ebi.ac.uk/efo/EFO_0020670 GCST90101462 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein E7_HPV16 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein e7_hpv16 measurement http://www.ebi.ac.uk/efo/EFO_0020671 GCST90101463 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein E7_HPV18 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein e7_hpv18 measurement http://www.ebi.ac.uk/efo/EFO_0020672 GCST90101464 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein FAM107A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein fam107a measurement http://www.ebi.ac.uk/efo/EFO_0020673 GCST90101465 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein FAM107B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein fam107b measurement http://www.ebi.ac.uk/efo/EFO_0020674 GCST90101466 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein jagged-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 protein jagged-1 measurement http://www.ebi.ac.uk/efo/EFO_0008271 GCST90101467 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein jagged-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein jagged-2 measurement http://www.ebi.ac.uk/efo/EFO_0020675 GCST90101468 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase B alpha/beta/gamma levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase b alpha/beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0020676 GCST90101469 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase C alpha type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase c alpha type measurement http://www.ebi.ac.uk/efo/EFO_0020677 GCST90101470 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase C beta type (splice variant beta-II) levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase c beta type (splice variant beta-II) measurement http://www.ebi.ac.uk/efo/EFO_0020678 GCST90101471 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase C delta type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase c delta type measurement http://www.ebi.ac.uk/efo/EFO_0020679 GCST90101472 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase C gamma type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase c gamma type measurement http://www.ebi.ac.uk/efo/EFO_0020680 GCST90101473 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase C iota type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase c iota type measurement http://www.ebi.ac.uk/efo/EFO_0020681 GCST90101474 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase C theta type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase c theta type measurement http://www.ebi.ac.uk/efo/EFO_0020682 GCST90101475 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Periostin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90101401 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peroxiredoxin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peroxiredoxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020629 GCST90101402 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peroxiredoxin-5, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peroxiredoxin-5, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020630 GCST90101403 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peroxiredoxin-6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peroxiredoxin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020631 GCST90101404 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Persephin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 persephin measurement http://www.ebi.ac.uk/efo/EFO_0020632 GCST90101405 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Persulfide dioxygenase ETHE1, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 persulfide dioxygenase ETHE1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008258 GCST90101406 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pescadillo homolog levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pescadillo homolog measurement http://www.ebi.ac.uk/efo/EFO_0020633 GCST90101407 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phosphatidylethanolamine-binding protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 phosphatidylethanolamine-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020634 GCST90101408 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase pten measurement http://www.ebi.ac.uk/efo/EFO_0020635 GCST90101409 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform:Phosphatidylinositol 3-kinase regulatory subunit alpha complex levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform:phosphatidylinositol 3-kinase regulatory subunit alpha complex measurement http://www.ebi.ac.uk/efo/EFO_0020636 GCST90101410 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform measurement http://www.ebi.ac.uk/efo/EFO_0020637 GCST90101411 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phosphoglycerate kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 phosphoglycerate kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020638 GCST90101412 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phosphoglycerate mutase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 phosphoglycerate mutase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020639 GCST90101413 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phospholipase A2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90101414 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Phospholipase A2, membrane associated levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90101415 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pituitary adenylate cyclase-activating polypeptide 27 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pituitary adenylate cyclase-activating polypeptide 27 measurement http://www.ebi.ac.uk/efo/EFO_0020640 GCST90101416 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pituitary adenylate cyclase-activating polypeptide 38 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pituitary adenylate cyclase-activating polypeptide 38 measurement http://www.ebi.ac.uk/efo/EFO_0020641 GCST90101417 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Placenta growth factor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 placenta growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010626 GCST90101418 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Plasma kallikrein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 plasma kallikrein measurement http://www.ebi.ac.uk/efo/EFO_0008260 GCST90101419 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Plasma protease C1 inhibitor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90101420 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Plasma serine protease inhibitor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 plasma serine protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0020642 GCST90101421 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Plasmin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 plasmin measurement http://www.ebi.ac.uk/efo/EFO_0020643 GCST90101422 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Plasminogen activator inhibitor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90101423 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Plasminogen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 plasma plasminogen measurement http://www.ebi.ac.uk/efo/EFO_0006309 GCST90101424 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Platelet endothelial cell adhesion molecule levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90101425 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NSFL1 cofactor p47 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 NFSL1 cofactor p47 measurement http://www.ebi.ac.uk/efo/EFO_0020612 GCST90101376 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NT-3 growth factor receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 nt-3 growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020613 GCST90101377 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Nuclear receptor subfamily 1 group D member 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 nuclear receptor subfamily 1 group d member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020614 GCST90101378 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Nucleoside diphosphate kinase A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 nucleoside diphosphate kinase A measurement http://www.ebi.ac.uk/efo/EFO_0009947 GCST90101379 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Nucleoside diphosphate kinase B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 nucleoside diphosphate kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020615 GCST90101380 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. NudC domain-containing protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 NudC domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020616 GCST90101381 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. OCIA domain-containing protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 OCIA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008252 GCST90101382 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Olfactomedin-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 olfactomedin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020617 GCST90101383 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Oncostatin-M levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90101384 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Opioid-binding protein/cell adhesion molecule levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 opioid-binding protein/cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020618 GCST90101385 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Osteomodulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 osteomodulin measurement http://www.ebi.ac.uk/efo/EFO_0020619 GCST90101386 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. OX-2 membrane glycoprotein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 OX-2 membrane glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008253 GCST90101387 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Oxidized low-density lipoprotein receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 oxidized low-density lipoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020620 GCST90101388 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. P-selectin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90101389 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pancreatic hormone levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pancreatic hormone measurement http://www.ebi.ac.uk/efo/EFO_0020621 GCST90101390 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pappalysin-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pappalysin‐1 measurement http://www.ebi.ac.uk/efo/EFO_0010618 GCST90101391 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Parathyroid hormone levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST90101392 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Parathyroid hormone-related protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 parathyroid hormone-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020622 GCST90101393 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peptide YY levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peptide yy measurement http://www.ebi.ac.uk/efo/EFO_0020623 GCST90101394 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peptidoglycan recognition protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90101395 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peptidyl-prolyl cis-trans isomerase A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peptidyl-prolyl cis-trans isomerase A measurement http://www.ebi.ac.uk/efo/EFO_0020625 GCST90101396 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peptidyl-prolyl cis-trans isomerase B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peptidyl-prolyl cis-trans isomerase B measurement http://www.ebi.ac.uk/efo/EFO_0020626 GCST90101397 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peptidyl-prolyl cis-trans isomerase D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 peptidyl-prolyl cis-trans isomerase D measurement http://www.ebi.ac.uk/efo/EFO_0008256 GCST90101398 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peptidyl-prolyl cis-trans isomerase E levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 peptidyl-prolyl cis-trans isomerase E measurement http://www.ebi.ac.uk/efo/EFO_0008257 GCST90101399 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Peptidyl-prolyl cis-trans isomerase F, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 peptidyl-prolyl cis-trans isomerase F, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020627 GCST90101400 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein kinase C zeta type levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein kinase c zeta type measurement http://www.ebi.ac.uk/efo/EFO_0020683 GCST90101476 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein lin-7 homolog B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90101477 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein NOV homolog levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein nov homolog measurement http://www.ebi.ac.uk/efo/EFO_0020685 GCST90101478 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein Rev_HV2BE levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein rev_hv2be measurement http://www.ebi.ac.uk/efo/EFO_0020686 GCST90101479 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein S100-A9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein s100-a9 measurement http://www.ebi.ac.uk/efo/EFO_0020687 GCST90101480 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein SET levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein set measurement http://www.ebi.ac.uk/efo/EFO_0020688 GCST90101481 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein Wnt-7a levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein wnt-7a measurement http://www.ebi.ac.uk/efo/EFO_0020689 GCST90101482 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein-glutamine gamma-glutamyltransferase E levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein-glutamine gamma-glutamyltransferase e measurement http://www.ebi.ac.uk/efo/EFO_0020690 GCST90101483 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Protein-tyrosine kinase 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 protein-tyrosine kinase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020691 GCST90101484 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Prothrombin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 prothrombin measurement http://www.ebi.ac.uk/efo/EFO_0020692 GCST90101485 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proto-oncogene tyrosine-protein kinase receptor Ret levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 proto-oncogene tyrosine-protein kinase receptor Ret measurement http://www.ebi.ac.uk/efo/EFO_0008272 GCST90101486 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Proto-oncogene tyrosine-protein kinase Src levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 proto-oncogene tyrosine-protein kinase Src measurement http://www.ebi.ac.uk/efo/EFO_0010927 GCST90101487 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pulmonary surfactant-associated protein D levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90101488 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pyridoxal phosphate phosphatase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pyridoxal phosphate phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0020694 GCST90101489 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Pyruvate kinase PKM levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 pyruvate kinase pkm measurement http://www.ebi.ac.uk/efo/EFO_0020695 GCST90101490 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. R-spondin-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 r-spondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020696 GCST90101491 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Rab GDP dissociation inhibitor beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 rab gdp dissociation inhibitor beta measurement http://www.ebi.ac.uk/efo/EFO_0020697 GCST90101492 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ras GTPase-activating protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ras GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020698 GCST90101493 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ras-related C3 botulinum toxin substrate 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ras-related c3 botulinum toxin substrate 1 measurement http://www.ebi.ac.uk/efo/EFO_0020699 GCST90101494 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Receptor tyrosine-protein kinase erbB-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 receptor tyrosine-protein kinase erbb-2 measurement http://www.ebi.ac.uk/efo/EFO_0020700 GCST90101495 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Receptor tyrosine-protein kinase erbB-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 receptor tyrosine-protein kinase erbb-3 measurement http://www.ebi.ac.uk/efo/EFO_0020701 GCST90101496 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Receptor tyrosine-protein kinase erbB-4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 receptor tyrosine-protein kinase erbb-4 measurement http://www.ebi.ac.uk/efo/EFO_0020702 GCST90101497 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Receptor-type tyrosine-protein kinase FLT3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 receptor-type tyrosine-protein kinase flt3 measurement http://www.ebi.ac.uk/efo/EFO_0020703 GCST90101498 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Renin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 renin measurement http://www.ebi.ac.uk/efo/EFO_0010616 GCST90101499 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Repulsive guidance molecule A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 repulsive guidance molecule A measurement http://www.ebi.ac.uk/efo/EFO_0008273 GCST90101500 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dynein light chain roadblock-type 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 dynein light chain roadblock-type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008114 GCST90100944 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. E-selectin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90100945 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. E3 ubiquitin-protein ligase Mdm2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 e3 ubiquitin-protein ligase mdm2 measurement http://www.ebi.ac.uk/efo/EFO_0020340 GCST90100946 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ectodysplasin-A, secreted form levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ectodysplasin-a, secreted form measurement http://www.ebi.ac.uk/efo/EFO_0020341 GCST90100947 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90100948 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ectonucleoside triphosphate diphosphohydrolase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020343 GCST90100949 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ectonucleoside triphosphate diphosphohydrolase 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90100950 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0020344 GCST90100951 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. EGF-like module-containing mucin-like hormone receptor-like 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 EGF-like module-containing mucin-like hormone receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0008116 GCST90100952 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Elafin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90100953 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Elongation factor 1-beta levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 elongation factor 1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020345 GCST90100954 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endoglin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 endoglin measurement http://www.ebi.ac.uk/efo/EFO_0008118 GCST90100955 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endoplasmic reticulum aminopeptidase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 6 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90100956 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endoplasmic reticulum resident protein 29 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 endoplasmic reticulum resident protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0020346 GCST90100957 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endostatin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 endostatin measurement http://www.ebi.ac.uk/efo/EFO_0020347 GCST90100958 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endothelial cell-selective adhesion molecule levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90100959 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endothelial cell-specific molecule 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 endothelial cell-specific molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010912 GCST90100960 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endothelial monocyte-activating polypeptide 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 endothelial monocyte-activating polypeptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020348 GCST90100961 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Endothelin-converting enzyme 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90100962 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Enteropeptidase levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 enteropeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020349 GCST90100963 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Eotaxin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90100964 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-A receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 ephrin type-A receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008123 GCST90100965 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-A receptor 10 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin type-a receptor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020350 GCST90100966 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-A receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin type-a receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020351 GCST90100967 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-A receptor 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin type-a receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020352 GCST90100968 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Desmocollin-3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 desmocollin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020320 GCST90100919 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Desmoglein-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 desmoglein-1 measurement http://www.ebi.ac.uk/efo/EFO_0020321 GCST90100920 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Desmoglein-2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 desmoglein-2 measurement http://www.ebi.ac.uk/efo/EFO_0020322 GCST90100921 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Diablo homolog, mitochondrial levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 diablo homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020323 GCST90100922 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dickkopf-like protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dickkopf-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020324 GCST90100923 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dickkopf-related protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90100924 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dickkopf-related protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90100925 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dickkopf-related protein 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 Dickkopf-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008110 GCST90100926 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dipeptidyl peptidase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dipeptidyl peptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020325 GCST90100927 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dipeptidyl peptidase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90100928 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Discoidin domain-containing receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 discoidin domain-containing receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020327 GCST90100929 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Disintegrin and metalloproteinase domain-containing protein 12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 disintegrin and metalloproteinase domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0020328 GCST90100930 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Disintegrin and metalloproteinase domain-containing protein 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 disintegrin and metalloproteinase domain-containing protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0020329 GCST90100931 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. DNA repair protein RAD51 homolog 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 DNA repair protein rad51 homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0020330 GCST90100932 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. DNA topoisomerase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 DNA topoisomerase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020331 GCST90100933 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. DnaJ homolog subfamily B member 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 DNAj homolog subfamily b member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020332 GCST90100934 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Drebrin-like protein levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 drebrin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020333 GCST90100935 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90100936 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dual specificity mitogen-activated protein kinase kinase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dual specificity mitogen-activated protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020335 GCST90100937 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dual specificity mitogen-activated protein kinase kinase 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 dual specificity mitogen-activated protein kinase kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008112 GCST90100938 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dual specificity mitogen-activated protein kinase kinase 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 3 dual specificity mitogen-activated protein kinase kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0008113 GCST90100939 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dual specificity protein phosphatase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dual specificity protein phosphatase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020336 GCST90100940 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dual specificity tyrosine-phosphorylation-regulated kinase 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dual specificity tyrosine-phosphorylation-regulated kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020337 GCST90100941 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dynactin subunit 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dynactin subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0020338 GCST90100942 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Dynein light chain 1, cytoplasmic levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 dynein light chain 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020339 GCST90100943 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-A receptor 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin type-a receptor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020353 GCST90100969 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-B receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90100970 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-B receptor 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin type-b receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020354 GCST90100971 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin type-B receptor 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90100972 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin-A4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin-A4 measurement http://www.ebi.ac.uk/efo/EFO_0020356 GCST90100973 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin-A5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin-A5 measurement http://www.ebi.ac.uk/efo/EFO_0020357 GCST90100974 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ephrin-B3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90100975 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Epidermal growth factor receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90100976 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Epidermal growth factor receptor substrate 15-like 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 epidermal growth factor receptor substrate 15-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020360 GCST90100977 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Epiregulin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 epiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020361 GCST90100978 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Epithelial discoidin domain-containing receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 epithelial discoidin domain-containing receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020362 GCST90100979 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Erythropoietin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 erythropoietin measurement http://www.ebi.ac.uk/efo/EFO_0020363 GCST90100980 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Erythropoietin receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 erythropoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020364 GCST90100981 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Estradiol 17-beta-dehydrogenase 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 estradiol 17-beta-dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020365 GCST90100982 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Estrogen receptor levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 estrogen receptor measurement http://www.ebi.ac.uk/efo/EFO_0008125 GCST90100983 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Eukaryotic initiation factor 4A-III levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 eukaryotic initiation factor 4a-III measurement http://www.ebi.ac.uk/efo/EFO_0020366 GCST90100984 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Eukaryotic translation initiation factor 4 gamma 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 eukaryotic translation initiation factor 4 gamma 2 measurement http://www.ebi.ac.uk/efo/EFO_0020367 GCST90100985 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Eukaryotic translation initiation factor 4E-binding protein 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 eukaryotic translation initiation factor 4E-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020368 GCST90100986 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Eukaryotic translation initiation factor 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 eukaryotic translation initiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020369 GCST90100987 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Eukaryotic translation initiation factor 5A-1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 eukaryotic translation initiation factor 5A-1 measurement http://www.ebi.ac.uk/efo/EFO_0020370 GCST90100988 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Extracellular matrix protein 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008126 GCST90100989 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. FACT complex subunit SSRP1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fact complex subunit ssrp1 measurement http://www.ebi.ac.uk/efo/EFO_0020371 GCST90100990 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fatty acid-binding protein, epidermal levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fatty acid-binding protein, epidermal measurement http://www.ebi.ac.uk/efo/EFO_0020372 GCST90100991 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fatty acid-binding protein, heart levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fatty acid-binding protein, heart measurement http://www.ebi.ac.uk/efo/EFO_0020373 GCST90100992 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fc receptor-like protein 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 Fc receptor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008127 GCST90100993 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Ferritin levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 2 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90100994 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fetuin-B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 fetuin-B measurement http://www.ebi.ac.uk/efo/EFO_0008128 GCST90100995 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibrinogen gamma chain levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibrinogen gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0020374 GCST90100996 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibrinogen levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90100997 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020375 GCST90100998 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 10 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020376 GCST90100999 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 12 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 12 measurement http://www.ebi.ac.uk/efo/EFO_0020377 GCST90101000 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 16 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90101001 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 17 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 17 measurement http://www.ebi.ac.uk/efo/EFO_0020379 GCST90101002 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 18 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 18 measurement http://www.ebi.ac.uk/efo/EFO_0020380 GCST90101003 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 19 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90101004 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 1 fibroblast growth factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008129 GCST90101005 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 20 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 20 measurement http://www.ebi.ac.uk/efo/EFO_0020381 GCST90101006 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 23 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90101007 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020382 GCST90101008 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 5 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90101009 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 6 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020383 GCST90101010 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 7 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90101011 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 8 isoform A levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor basic measurement http://www.ebi.ac.uk/efo/EFO_0008130 GCST90101012 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 8 isoform B levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 8 isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020386 GCST90101013 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor 9 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020387 GCST90101014 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor receptor 1 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020388 GCST90101015 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor receptor 2 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020389 GCST90101016 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor receptor 3 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90101017 Genome-wide genotyping array 2022-04-11 28240269 Suhre K 2017-02-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28240269 Connecting genetic risk to disease end points through the human blood plasma proteome. Fibroblast growth factor receptor 4 levels 997 European ancestry individuals 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals Affymetrix [509946] 0 fibroblast growth factor receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020391 GCST90101018 Genome-wide genotyping array 2022-04-28 35017462 Meng P 2022-01-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35017462 Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data. Mental disorders (time to event) 56,863 British ancestry cases, 319,943 British ancestry controls NA Affymetrix [NR] (imputed) 1 age at diagnosis, mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0004918, http://www.ebi.ac.uk/efo/EFO_0000677 GCST90102280 Genome-wide genotyping array 2022-04-28 35017462 Meng P 2022-01-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35017462 Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data. Anxiety (time to event) 13,463 British ancestry cases, 363,343 British ancestry controls NA Affymetrix [NR] (imputed) 0 age at diagnosis, anxiety http://www.ebi.ac.uk/efo/EFO_0004918, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90102281 Genome-wide genotyping array 2022-04-28 35017462 Meng P 2022-01-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35017462 Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data. Depression (time to event) 31,414 British ancestry cases, 345,392 British ancestry controls NA Affymetrix [NR] (imputed) 3 age at diagnosis, unipolar depression http://www.ebi.ac.uk/efo/EFO_0004918, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90102282 Genome-wide genotyping array 2022-04-28 35017462 Meng P 2022-01-11 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35017462 Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data. Substance use disorders (time to event) 17,604 British ancestry cases, 359,202 British ancestry controls NA Affymetrix [NR] (imputed) 12 age at diagnosis, substance-related disorder http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0002494 GCST90102283 Genome-wide genotyping array 2022-07-19 35448080 Lee SB 2022-03-30 J Cardiovasc Dev Dis www.ncbi.nlm.nih.gov/pubmed/35448080 Genome-Wide Association of New-Onset Hypertension According to Renin Concentration: The Korean Genome and Epidemiology Cohort Study. New onset hypertension 1,704 Korean ancestry cases, 3,507 Korean ancestry controls NA Affymetrix [NR] (imputed) 3 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90128468 Genome-wide genotyping array 2022-07-19 35448080 Lee SB 2022-03-30 J Cardiovasc Dev Dis www.ncbi.nlm.nih.gov/pubmed/35448080 Genome-Wide Association of New-Onset Hypertension According to Renin Concentration: The Korean Genome and Epidemiology Cohort Study. New onset hypertension (low renin group) 1,294 Korean ancestry cases, 2,372 Korean ancestry controls NA Affymetrix [NR] (imputed) 4 renin measurement, hypertension http://www.ebi.ac.uk/efo/EFO_0010616, http://www.ebi.ac.uk/efo/EFO_0000537 GCST90128469 Genome-wide genotyping array 2022-07-19 35448080 Lee SB 2022-03-30 J Cardiovasc Dev Dis www.ncbi.nlm.nih.gov/pubmed/35448080 Genome-Wide Association of New-Onset Hypertension According to Renin Concentration: The Korean Genome and Epidemiology Cohort Study. New onset hypertension (high renin group) 410 Korean ancestry cases, 1,135 Korean ancestry controls NA Affymetrix [NR] (imputed) 2 renin measurement, hypertension http://www.ebi.ac.uk/efo/EFO_0010616, http://www.ebi.ac.uk/efo/EFO_0000537 GCST90128470 Genome-wide genotyping array 2022-05-24 35223824 Carlson JC 2022-02-10 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/35223824 Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk. Orofacial cleft x maternal alcohol consumption interaction (2df) 119 European ancestry exposed cases, 225 European ancestry unexposed cases, 66 European ancestry exposed controls, 128 European ancestry unexposed controls NA Illumina [5165675] (imputed) 0 orofacial cleft, alcohol exposure measurement http://purl.obolibrary.org/obo/MONDO_0000358, http://www.ebi.ac.uk/efo/EFO_0009113 GCST90103788 Genome-wide genotyping array 2022-05-24 35223824 Carlson JC 2022-02-10 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/35223824 Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk. Orofacial cleft x maternal smoking interaction (2df) 89 European ancestry exposed cases, 255 European ancestry unexposed cases, 59 European ancestry exposed controls, 135 European ancestry unexposed controls NA Illumina [5165675] (imputed) 0 orofacial cleft, tobacco smoke exposure measurement http://purl.obolibrary.org/obo/MONDO_0000358, http://www.ebi.ac.uk/efo/EFO_0009115 GCST90103789 Genome-wide genotyping array 2022-05-24 35223824 Carlson JC 2022-02-10 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/35223824 Genome-wide Interaction Study Implicates VGLL2 and Alcohol Exposure and PRL and Smoking in Orofacial Cleft Risk. Orofacial cleft x maternal vitamin supplementation interaction (2df) 292 European ancestry exposed cases, 52 European ancestry unexposed cases, 128 European ancestry exposed controls, 66 European ancestry unexposed controls NA Illumina [5165675] (imputed) 1 orofacial cleft, vitamin supplement exposure measurement http://purl.obolibrary.org/obo/MONDO_0000358, http://www.ebi.ac.uk/efo/EFO_0009116 GCST90103790 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum aluminum levels 1,775 East Asian ancestry individuals NA Illumina [6148846] (imputed) 7 blood aluminium measurement http://www.ebi.ac.uk/efo/EFO_0007575 GCST90100517 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum arsenic levels 1,773 East Asian ancestry individuals NA Illumina [6148846] (imputed) 7 blood arsenic measurement http://www.ebi.ac.uk/efo/EFO_0021527 GCST90100518 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum barium levels 1,792 East Asian ancestry individuals NA Illumina [6148846] (imputed) 11 blood barium measurement http://www.ebi.ac.uk/efo/EFO_0021528 GCST90100519 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum calcium levels 1,740 East Asian ancestry individuals NA Illumina [6148846] (imputed) 16 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90100520 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum cadmium levels 1,775 East Asian ancestry individuals NA Illumina [6148846] (imputed) 9 blood cadmium measurement http://www.ebi.ac.uk/efo/EFO_0007576 GCST90100521 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum cobalt levels 1,758 East Asian ancestry individuals NA Illumina [6148846] (imputed) 11 blood cobalt measurement http://www.ebi.ac.uk/efo/EFO_0007577 GCST90100522 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum chromium levels 1,758 East Asian ancestry individuals NA Illumina [6148846] (imputed) 15 blood chromium measurement http://www.ebi.ac.uk/efo/EFO_0007579 GCST90100523 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum copper levels 1,798 East Asian ancestry individuals NA Illumina [6148846] (imputed) 22 blood copper measurement http://www.ebi.ac.uk/efo/EFO_0007578 GCST90100524 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum iron levels 1,794 East Asian ancestry individuals NA Illumina [6148846] (imputed) 11 serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006332 GCST90100525 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum magnesium levels 1,791 East Asian ancestry individuals NA Illumina [6148846] (imputed) 4 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST90100526 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum manganese levels 1,674 East Asian ancestry individuals NA Illumina [6148846] (imputed) 8 blood manganese measurement http://www.ebi.ac.uk/efo/EFO_0007581 GCST90100527 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum molybdenum levels 1,752 East Asian ancestry individuals NA Illumina [6148846] (imputed) 21 blood molybdenum measurement http://www.ebi.ac.uk/efo/EFO_0007582 GCST90100528 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum nickel levels 1,756 East Asian ancestry individuals NA Illumina [6148846] (imputed) 20 blood nickel measurement http://www.ebi.ac.uk/efo/EFO_0007583 GCST90100529 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum lead levels 1,765 East Asian ancestry individuals NA Illumina [6148846] (imputed) 15 blood lead measurement http://www.ebi.ac.uk/efo/EFO_0007040 GCST90100530 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum rubidium levels 1,795 East Asian ancestry individuals NA Illumina [6148846] (imputed) 11 blood rubidium measurement http://www.ebi.ac.uk/efo/EFO_0021529 GCST90100531 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum selenium levels 1,799 East Asian ancestry individuals NA Illumina [6148846] (imputed) 13 serum selenium measurement http://www.ebi.ac.uk/efo/EFO_0005266 GCST90100532 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum tin levels 1,793 East Asian ancestry individuals NA Illumina [6148846] (imputed) 9 blood tin measurement http://www.ebi.ac.uk/efo/EFO_0021530 GCST90100533 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum strontium levels 1,797 East Asian ancestry individuals NA Illumina [6148846] (imputed) 14 blood strontium measurement http://www.ebi.ac.uk/efo/EFO_0021531 GCST90100534 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum titanium levels 1,796 East Asian ancestry individuals NA Illumina [6148846] (imputed) 10 blood titanium measurement http://www.ebi.ac.uk/efo/EFO_0021532 GCST90100535 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum vanadium levels 1,800 East Asian ancestry individuals NA Illumina [6148846] (imputed) 13 blood vanadium measurement http://www.ebi.ac.uk/efo/EFO_0021533 GCST90100536 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Serum zinc levels 1,798 East Asian ancestry individuals NA Illumina [6148846] (imputed) 11 blood zinc measurement http://www.ebi.ac.uk/efo/EFO_0007584 GCST90100537 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma aluminum levels 678 East Asian ancestry individuals NA Illumina [4338913] (imputed) 3 blood aluminium measurement http://www.ebi.ac.uk/efo/EFO_0007575 GCST90100538 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma arsenic levels 676 East Asian ancestry individuals NA Illumina [4338913] (imputed) 6 blood arsenic measurement http://www.ebi.ac.uk/efo/EFO_0021527 GCST90100539 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma barium levels 687 East Asian ancestry individuals NA Illumina [4338913] (imputed) 9 blood barium measurement http://www.ebi.ac.uk/efo/EFO_0021528 GCST90100540 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma calcium levels 688 East Asian ancestry individuals NA Illumina [4338913] (imputed) 8 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90100541 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma cadmium levels 656 East Asian ancestry individuals NA Illumina [4338913] (imputed) 9 blood cadmium measurement http://www.ebi.ac.uk/efo/EFO_0007576 GCST90100542 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma cobalt levels 639 East Asian ancestry individuals NA Illumina [4338913] (imputed) 9 blood cobalt measurement http://www.ebi.ac.uk/efo/EFO_0007577 GCST90100543 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma chromium levels 685 East Asian ancestry individuals NA Illumina [4338913] (imputed) 6 blood chromium measurement http://www.ebi.ac.uk/efo/EFO_0007579 GCST90100544 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma copper levels 685 East Asian ancestry individuals NA Illumina [4338913] (imputed) 12 blood copper measurement http://www.ebi.ac.uk/efo/EFO_0007578 GCST90100545 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma iron levels 687 East Asian ancestry individuals NA Illumina [4338913] (imputed) 8 serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006332 GCST90100546 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma magnesium levels 688 East Asian ancestry individuals NA Illumina [4338913] (imputed) 4 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST90100547 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma manganese levels 681 East Asian ancestry individuals NA Illumina [4338913] (imputed) 11 blood manganese measurement http://www.ebi.ac.uk/efo/EFO_0007581 GCST90100548 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma molybdenum levels 682 East Asian ancestry individuals NA Illumina [4338913] (imputed) 4 blood molybdenum measurement http://www.ebi.ac.uk/efo/EFO_0007582 GCST90100549 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma nickel levels 685 East Asian ancestry individuals NA Illumina [4338913] (imputed) 13 blood nickel measurement http://www.ebi.ac.uk/efo/EFO_0007583 GCST90100550 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma lead levels 676 East Asian ancestry individuals NA Illumina [4338913] (imputed) 8 blood lead measurement http://www.ebi.ac.uk/efo/EFO_0007040 GCST90100551 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma rubidium levels 688 East Asian ancestry individuals NA Illumina [4338913] (imputed) 10 blood rubidium measurement http://www.ebi.ac.uk/efo/EFO_0021529 GCST90100552 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma selenium levels 688 East Asian ancestry individuals NA Illumina [4338913] (imputed) 11 serum selenium measurement http://www.ebi.ac.uk/efo/EFO_0005266 GCST90100553 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma tin levels 667 East Asian ancestry individuals NA Illumina [4338913] (imputed) 3 blood tin measurement http://www.ebi.ac.uk/efo/EFO_0021530 GCST90100554 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma strontium levels 687 East Asian ancestry individuals NA Illumina [4338913] (imputed) 5 blood strontium measurement http://www.ebi.ac.uk/efo/EFO_0021531 GCST90100555 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma titanium levels 688 East Asian ancestry individuals NA Illumina [4338913] (imputed) 12 blood titanium measurement http://www.ebi.ac.uk/efo/EFO_0021532 GCST90100556 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma vanadium levels 688 East Asian ancestry individuals NA Illumina [4338913] (imputed) 7 blood vanadium measurement http://www.ebi.ac.uk/efo/EFO_0021533 GCST90100557 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Plasma zinc levels 684 East Asian ancestry individuals NA Illumina [4338913] (imputed) 5 blood zinc measurement http://www.ebi.ac.uk/efo/EFO_0007584 GCST90100558 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Copper levels 2,483 East Asian ancestry individuals NA Illumina [6148846] (imputed) 4 blood copper measurement http://www.ebi.ac.uk/efo/EFO_0007578 GCST90104088 Genome-wide genotyping array 2022-07-13 35501403 Yang W 2022-05-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35501403 Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans. Manganese levels 2,355 East Asian ancestry individuals NA Illumina [6148846] (imputed) 0 blood manganese measurement http://www.ebi.ac.uk/efo/EFO_0007581 GCST90104089 Genome-wide genotyping array 2022-04-06 35379992 Bellenguez C 2022-04-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35379992 New insights into the genetic etiology of Alzheimer's disease and related dementias. Alzheimer's disease 39,106 European ancestry clinically diagnosed cases, 46,828 European ancestry proxy cases, 401,577 European ancestry controls 25,392 cases, 276,086 controls Affymetrix, Illumina [21101114] (imputed) 89 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90027158 Genome-wide genotyping array 2022-02-24 34718232 Sun ED 2021-10-29 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/34718232 Predicting physiological aging rates from a range of quantitative traits using machine learning. Physiological aging rate up to 6,100 European ancestry individuals NA NR [NR] 2 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90094987 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:3) [NL-18:2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90025797 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:4) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90025798 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:4) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90025799 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (53:2) [NL-17:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90025800 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:0) [NL-18:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 54:0 measurement http://www.ebi.ac.uk/efo/EFO_0021485 GCST90025801 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:1) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 54:1 measurement http://www.ebi.ac.uk/efo/EFO_0010419 GCST90025802 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:2) [NL-18:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 54:2 measurement http://www.ebi.ac.uk/efo/EFO_0010420 GCST90025803 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (24:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90024801 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (24:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90024802 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (26:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 26:0 measurement http://www.ebi.ac.uk/efo/EFO_0021464 GCST90024803 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (26:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 26:0 measurement http://www.ebi.ac.uk/efo/EFO_0021464 GCST90024804 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024805 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024806 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024807 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024808 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-20:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024809 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024810 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-22:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024811 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024812 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024813 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkylphosphatidylcholine (O-24:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024814 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024815 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024816 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024817 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylcholine (P-20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024818 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-16:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025772 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025773 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:3) [NL-16:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90025774 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:3) [NL-18:2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90025775 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-15:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90025776 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90025777 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90025778 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:0) [NL-18:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 50:0 measurement http://www.ebi.ac.uk/efo/EFO_0021480 GCST90025779 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:1) [NL-14:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90025780 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:1) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90025781 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90025782 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90025783 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90025784 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-14:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90025785 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-16:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90025786 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90025787 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:4) [NL-14:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90025788 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:0) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 51:0 measurement http://www.ebi.ac.uk/efo/EFO_0021481 GCST90025789 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:1) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90025790 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-15:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90025791 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90025792 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90025793 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:1) [NL-18:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 52:1 measurement http://www.ebi.ac.uk/efo/EFO_0010413 GCST90025794 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:2) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90025795 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:3) [NL-16:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90025796 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (16:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90024819 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (16:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90024820 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (17:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 lysophosphatidylethanolamine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021465 GCST90024821 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (17:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021465 GCST90024822 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90024823 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90024824 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:1) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90024825 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:1) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90024826 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:2) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90024827 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (18:2) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90024828 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (20:4) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90024829 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (20:4) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90024830 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (22:6) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90024831 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylethanolamine (22:6) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90024832 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024833 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024834 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024835 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysoalkenylphosphatidylethanolamine (P-20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90024836 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024837 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024838 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:1) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024839 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:1) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024840 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:2) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024841 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (18:2) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024842 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (20:4) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024843 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/20:0) levels/Sphingomyelin (d16:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025747 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/22:0) levels/Sphingomyelin (d16:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025748 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/23:0) levels/Sphingomyelin (d17:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025749 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025750 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025751 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025752 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025753 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/17:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025754 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025755 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025756 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025757 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025758 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/23:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025759 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025760 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d19:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025761 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025762 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/16:0(OH) levels) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025763 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025764 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:0(OH) levels) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025765 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025766 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:1(OH) levels) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025767 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:0) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90025768 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:1) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90025769 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-14:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025770 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025771 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:2) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021458 GCST90024782 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:2) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021458 GCST90024783 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:3) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90024784 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:3) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90024785 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:4) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90024786 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:4) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90024787 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:5) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90024788 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (20:5) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90024789 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021459 GCST90024790 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021459 GCST90024791 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:1) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021460 GCST90024792 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:1) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021460 GCST90024793 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:4) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90024794 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:4) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90024795 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn1] (n3) levels/Lysophosphatidylcholine (22:5) [sn2] (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90024796 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn1] (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90024797 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:5) [sn2] (n3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90024798 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:6) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90024799 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (22:6) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90024800 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025741 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025742 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/14:0) levels/Sphingomyelin (d16:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025743 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025744 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/17:0) levels/Sphingomyelin (d17:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025745 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/18:0) levels/Sphingomyelin (d16:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025746 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025620 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025621 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025622 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025623 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025624 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025625 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/22:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025626 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025627 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:1/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025628 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:1/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025629 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-34:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025630 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-36:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025631 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-38:5) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025632 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-38:5) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025633 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025634 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/22:6) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025635 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/22:6) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025636 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025637 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025638 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025639 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025640 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025641 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025642 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025643 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025644 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:5) (n3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025645 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:5) (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025646 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025647 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/20:4) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025648 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/20:4) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025649 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/22:6) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025650 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/22:6) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025651 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025652 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025653 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025654 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025655 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:3) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025656 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025657 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025658 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025659 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:5) (n3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025660 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:5) (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025661 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025662 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025663 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:1) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025664 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:1) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025665 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:2) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025666 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:2) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025667 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025668 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:3) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025669 Genome-wide genotyping array 2022-04-29 35019943 Pardinas AF 2022-01-12 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/35019943 Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia. Treatment-resistant schizophrenia 10,501 European ancestry cases, 24,542 European ancestry controls NA NR [NR] (imputed) 0 treatment refractory schizophrenia http://www.ebi.ac.uk/efo/EFO_0004609 GCST90102461 Genome-wide genotyping array 2022-04-29 35019943 Pardinas AF 2022-01-12 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/35019943 Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia. Non treatment-resistant schizophrenia 20,325 European ancestry cases, 30,122 European ancestry controls NA NR [NR] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90102462 Genome-wide genotyping array 2022-04-29 35019943 Pardinas AF 2022-01-12 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/35019943 Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia. Schizophrenia x treatment resistance interaction 10,501 European ancestry treatment-resistant schizophrenia cases, 20,325 European ancestry non treatment-resistant schizophrenia cases, 54,664 European ancestry controls NA NR [NR] (imputed) 0 schizophrenia, response to xenobiotic stimulus http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/GO_0009410 GCST90102463 Genome-wide genotyping array 2022-04-12 35396452 Sarnowski C 2022-04-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35396452 Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels. Circulating levels of total-tau 14,721 European ancestry individuals NA NR [10082601] (imputed) 6 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST90095138 Genome-wide genotyping array 2022-04-12 35396452 Sarnowski C 2022-04-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35396452 Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels. Circulating levels of total-tau 953 African American individuals NA NR [12161902] (imputed) 14 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST90095139 Genome-wide genotyping array 2022-02-07 33619548 Oldoni F 2021-02-23 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/33619548 Genetic and Metabolic Determinants of Plasma Levels of ANGPTL8. Plasma ANGPTL8 levels 1,779 African American individuals, 1,022 European ancestry individuals, 589 Hispanic or Latin American individuals, 67 individuals NA NR [346167] 3 ANGPTL8 measurement http://www.ebi.ac.uk/efo/EFO_0020861 GCST90093122 Exome-wide sequencing 2022-04-04 34783190 Wang YF 2021-11-15 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/34783190 Multi-ancestral GWAS identifies shared and Asian-specific loci for SLE and links type III interferon signaling and lysosomal function to the disease. Systemic lupus erythematosus 4,734 Chinese ancestry cases, 9,425 Chinese ancestry controls, 835 Thai ancestry cases, 2,995 Thai ancestry controls NA NR [NR] (imputed) 4 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90100585 Genome-wide genotyping array 2022-04-04 34783190 Wang YF 2021-11-15 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/34783190 Multi-ancestral GWAS identifies shared and Asian-specific loci for SLE and links type III interferon signaling and lysosomal function to the disease. Systemic lupus erythematosus 4,734 Chinese ancestry cases, 9,425 Chinese ancestry controls, 835 Thai ancestry cases, 2,995 Thai ancestry controls, 4,576 European ancestry cases, 8,039 European ancestry controls NA NR [NR] (imputed) 6 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90100586 Genome-wide genotyping array 2022-05-09 34815255 Hong W 2021-11-23 Cancer Res www.ncbi.nlm.nih.gov/pubmed/34815255 Clonal Hematopoiesis Mutations in Patients with Lung Cancer Are Associated with Lung Cancer Risk Factors. Number of clonal hematopoiesis mutations 1,958 individuals NA Illumina [150292] 41 clonal hematopoiesis mutation measurement http://www.ebi.ac.uk/efo/EFO_0020949 GCST90100218 Genome-wide genotyping array, Exome-wide sequencing 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 66 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093032 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 65 very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90093033 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 74 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90093034 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of very small VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 70 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093035 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 78 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90093036 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 67 very low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90093037 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 94 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093038 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 96 triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093039 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in chylomicrons and extremely large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 82 chylomicron measurement, total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093040 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in chylomicrons and extremely large VLDL 111,638 European ancestry individuals NA NR [11722792] (imputed) 34 chylomicron measurement, very low density lipoprotein cholesterol measurement, cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020943 GCST90093041 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in chylomicrons and extremely large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 83 cholesteryl ester measurement, chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093042 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in chylomicrons and extremely large VLDL 111,638 European ancestry individuals NA NR [11722792] (imputed) 25 chylomicron measurement, very low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90093043 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in chylomicrons and extremely large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 82 free cholesterol measurement, chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093044 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in chylomicrons and extremely large VLDL 111,638 European ancestry individuals NA NR [11722792] (imputed) 33 chylomicron measurement, very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90093045 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in chylomicrons and extremely large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 77 chylomicron measurement, very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90093046 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of chylomicrons and extremely large VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 81 chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093047 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in chylomicrons and extremely large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 81 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90093048 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in chylomicrons and extremely large VLDL 111,638 European ancestry individuals NA NR [11722792] (imputed) 46 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90093049 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in chylomicrons and extremely large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 77 chylomicron measurement, triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093050 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in chylomicrons and extremely large VLDL 111,638 European ancestry individuals NA NR [11722792] (imputed) 30 chylomicron measurement, triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093051 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Acetate levels 115,050 European ancestry individuals NA NR [11722792] (imputed) 12 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90092803 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Acetoacetate levels 115,079 European ancestry individuals NA NR [11722792] (imputed) 7 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90092804 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Acetone levels 115,079 European ancestry individuals NA NR [11722792] (imputed) 15 acetone measurement http://www.ebi.ac.uk/efo/EFO_0010989 GCST90092805 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Alanine levels 115,078 European ancestry individuals NA NR [11722792] (imputed) 37 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90092806 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Albumin levels 115,064 European ancestry individuals NA NR [11722792] (imputed) 38 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90092807 Genome-wide genotyping array 2022-05-09 35007327 Lopez de Lapuente Portilla A 2022-01-10 Blood www.ncbi.nlm.nih.gov/pubmed/35007327 Genome-wide association study on 13,167 individuals identifies regulators of blood CD34+ cell levels. Peripheral blood CD34+ cell levels 10,949 Swedish ancestry individuals 2,218 Danish ancestry, Norwegian ancestry, Irish ancestry, Dutch ancestry, British ancestry individuals Illumina [18000000] (imputed) 9 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90102460 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 85 triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092979 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Saturated fatty acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 68 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092980 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of saturated fatty acids to total fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 28 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092981 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Sphingomyelin levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 69 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90092982 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of triglycerides to phosphoglycerides 115,006 European ancestry individuals NA NR [11722792] (imputed) 109 triglyceride measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092983 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total concentration of branched-chain amino acids (leucine + isoleucine + valine) 115,051 European ancestry individuals NA NR [11722792] (imputed) 20 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90092984 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total fatty acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 78 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092987 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in lipoprotein particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 73 lipid measurement, lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004732 GCST90092989 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total concentration of lipoprotein particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 68 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90092990 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total phospholipid levels in lipoprotein particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 67 lipoprotein measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004732, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092991 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total triglycerides levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 88 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90092992 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Tyrosine levels 114,913 European ancestry individuals NA NR [11722792] (imputed) 36 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90092993 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Degree of unsaturation 115,006 European ancestry individuals NA NR [11722792] (imputed) 47 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90092994 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Valine levels 115,052 European ancestry individuals NA NR [11722792] (imputed) 20 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90092995 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. VLDL cholesterol levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 72 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092996 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 66 cholesteryl ester measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092997 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 79 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092998 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 86 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092999 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 80 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093000 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 83 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90093001 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Average diameter for VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 94 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90093002 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 91 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093003 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in very large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 111 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093004 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in very large HDL 115,056 European ancestry individuals NA NR [11722792] (imputed) 56 cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093005 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in very large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 117 cholesteryl ester measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093006 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in very large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 82 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093016 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in very large VLDL 114,160 European ancestry individuals NA NR [11722792] (imputed) 87 very low density lipoprotein cholesterol measurement, cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020943 GCST90093017 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in very large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 81 cholesteryl ester measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093018 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in very large VLDL 114,160 European ancestry individuals NA NR [11722792] (imputed) 82 very low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90093019 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in very large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 82 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093020 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in very large VLDL 114,160 European ancestry individuals NA NR [11722792] (imputed) 72 very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90093021 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in very large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 86 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90093022 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of very large VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 88 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093023 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in very large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 83 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90093024 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in very large VLDL 114,160 European ancestry individuals NA NR [11722792] (imputed) 59 very low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90093025 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in very large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 97 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093026 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in very large VLDL 114,160 European ancestry individuals NA NR [11722792] (imputed) 72 triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093027 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 64 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093028 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 93 very low density lipoprotein cholesterol measurement, cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020943 GCST90093029 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 65 cholesteryl ester measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90093030 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in very small VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 100 very low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90093031 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in very large HDL 115,056 European ancestry individuals NA NR [11722792] (imputed) 51 cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020944, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093007 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in very large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 90 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093008 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in very large HDL 115,056 European ancestry individuals NA NR [11722792] (imputed) 104 free cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020945, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093009 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in very large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 103 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093010 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of very large HDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 100 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093011 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in very large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 103 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093012 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in very large HDL 115,056 European ancestry individuals NA NR [11722792] (imputed) 84 phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020946, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093013 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in very large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 72 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093014 Genome-wide genotyping array 2022-05-06 35022648 Skotte L 2022-01-12 Brain www.ncbi.nlm.nih.gov/pubmed/35022648 Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes. Febrile seizures 4,502 Danish ancestry cases, 51,049 Danish ancestry controls 3,133 European ancestry cases, 32,917 European ancestry controls Illumina [6799883] (imputed) 7 Febrile seizure (within the age range of 3 months to 6 years) http://purl.obolibrary.org/obo/HP_0002373 GCST90102486 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in very large HDL 115,056 European ancestry individuals NA NR [11722792] (imputed) 91 triglycerides:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90093015 Genome-wide genotyping array 2022-05-17 35241825 Horowitz JE 2022-03-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35241825 Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. COVID-19 (covid vs negative) 52,630 East Asian ancestry cases, 109,605 East Asian ancestry controls, 52,630 European ancestry cases, 109,605 European ancestry controls, 52,630 Hispanic or Latin American cases, 109,605 Hispanic or Latin American controls, 52,630 South Asian ancestry cases, 109,605 South Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103428 Genome-wide genotyping array 2022-05-17 35241825 Horowitz JE 2022-03-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35241825 Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. COVID-19 (severe vs negative or unknown) 2,184 East Asian ancestry cases, 689,620 East Asian ancestry controls, 2,184 European ancestry cases, 689,620 European ancestry controls, 2,184 Hispanic or Latin American cases, 689,620 Hispanic or Latin American controls, 2,184 South Asian ancestry cases, 689,620 South Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103431 Genome-wide genotyping array 2022-05-17 35241825 Horowitz JE 2022-03-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35241825 Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. COVID-19 (covid vs negative or unknown) 45,006 European ancestry cases, 651,358 European ancestry controls, 2,710 African ancestry cases, 26,106 African ancestry controls, 830 South Asian ancestry cases, 10,143 South Asian ancestry controls, 174 East Asian ancestry cases, 2,779 East Asian ancestry controls, 3,832 Hispanic or Latin American cases, 14,630 Hispanic or Latin American controls NA Affymetrix, Illumina [NR] (imputed) 3 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90096800 Genome-wide genotyping array 2022-05-17 35241825 Horowitz JE 2022-03-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35241825 Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. COVID-19 (not hospitalized vs negative or unknown) 38,865 European ancestry cases, 651,358 European ancestry controls, 2,295 African ancestry cases, 26,106 African ancestry controls, 674 South Asian ancestry cases, 10,143 South Asian ancestry controls, 174 East Asian ancestry cases, 2,779 East Asian ancestry controls, 3,633 Hispanic or Latin American cases, 14,630 Hispanic or Latin American controls NA Affymetrix, Illumina [NR] (imputed) 4 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103429 Genome-wide genotyping array 2022-05-17 35241825 Horowitz JE 2022-03-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35241825 Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease. COVID-19 (hospitalized vs negative or unknown) 6,141 European ancestry cases, 651,358 European ancestry controls, 415 African ancestry cases, 26,106 African ancestry controls, 156 South Asian ancestry cases, 10,143 South Asian ancestry controls, 199 Hispanic or Latin American cases, 14,630 Hispanic or Latin American controls NA Affymetrix, Illumina [NR] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103430 Genome-wide genotyping array 2022-04-29 35414057 He YQ 2022-04-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35414057 A polygenic risk score for nasopharyngeal carcinoma shows potential for risk stratification and personalized screening. Nasopharyngeal carcinoma 4,506 East Asian ancestry cases, 5,384 East Asian ancestry controls NA Illumina [19904290] (imputed) 0 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST90093313 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylethanolamine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025836 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkylphosphatidylethanolamine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025837 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkenylphosphatidylethanolamine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025838 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylglycerol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025839 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylinositol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025840 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylserine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025841 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Sphingomyelin levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025842 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Sulfatide levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025843 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Triacylglycerol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90025844 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkyldiacylglycerol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025845 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Trihexosylcermide levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025846 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Ubiquinone levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90025847 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ubiquinone levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90025848 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024862 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024863 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024864 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024865 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024866 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024867 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:1_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024868 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024869 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024870 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024871 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024872 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (17:1_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024873 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/23:0) levels/Sphingomyelin (d17:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025735 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025736 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025737 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025738 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025739 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025740 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024738 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024739 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024740 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024741 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Trihexosylcermide (d18:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024742 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024743 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024744 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024745 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024746 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024747 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Monohexosylceramide (d18:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90024748 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (14:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90024749 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (14:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90024750 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 3 lysophosphatidylcholine 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0020941 GCST90024751 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 lysophosphatidylcholine 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0020941 GCST90024752 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn1] [104_sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90024753 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn1] levels /Lysophosphatidylcholine (17:0) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90024754 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (15-MHDA) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90024755 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylcholine (16:0) [sn1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90024756 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Lysophosphatidylinositol (20:4) [sn2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90024844 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024845 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024846 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (14:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024847 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024848 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024849 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024850 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024851 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024852 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024853 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (15-MHDA_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024854 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024855 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024856 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024857 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024858 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024859 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_18:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024860 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (16:0_20:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024861 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:3) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90025804 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:4) [NL-18:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90025805 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:4) [NL-18:2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90025806 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:5) [NL-18:1] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90025807 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:6) [NL-18:2] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90025808 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (56:6) [NL-20:4] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 5 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90025809 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (56:8) [NL-20:4] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90025810 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (34:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine 34:5 measurement http://www.ebi.ac.uk/efo/EFO_0021471 GCST90024899 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (35:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 35:5 measurement http://www.ebi.ac.uk/efo/EFO_0021472 GCST90024900 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (36:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine 36:0 measurement http://www.ebi.ac.uk/efo/EFO_0021473 GCST90024901 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (36:6) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 36:6 measurement http://www.ebi.ac.uk/efo/EFO_0021474 GCST90024902 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 38:2 measurement http://www.ebi.ac.uk/efo/EFO_0010384 GCST90024903 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:4) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0010386 GCST90024904 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0010387 GCST90024905 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0010387 GCST90024906 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:6) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine 38:6 measurement http://www.ebi.ac.uk/efo/EFO_0010388 GCST90024907 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (38:7) (c) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 38:7 measurement http://www.ebi.ac.uk/efo/EFO_0021475 GCST90024908 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (39:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 39:5 measurement http://www.ebi.ac.uk/efo/EFO_0021476 GCST90024909 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (39:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 39:5 measurement http://www.ebi.ac.uk/efo/EFO_0021476 GCST90024910 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (40:7) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine 40:7 measurement http://www.ebi.ac.uk/efo/EFO_0021477 GCST90024911 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (40:8) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 40:8 measurement http://www.ebi.ac.uk/efo/EFO_0021478 GCST90024912 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024913 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024914 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024915 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-16:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024916 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024917 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024918 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024919 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024920 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:1/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024921 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-18:1/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024922 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-32:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024923 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024874 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024875 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024876 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 13 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024877 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024878 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:5) (n3) levels/Phosphatidylcholine (20:1_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024879 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:5) (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024880 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024881 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024882 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024883 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024884 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_22:6) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024885 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:1_22:6) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024886 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:2_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024887 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (18:2_20:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024888 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (20:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024889 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (28:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 28:0 measurement http://www.ebi.ac.uk/efo/EFO_0021466 GCST90024890 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (31:0) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 31:0 measurement http://www.ebi.ac.uk/efo/EFO_0021467 GCST90024891 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (31:0) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 31:0 measurement http://www.ebi.ac.uk/efo/EFO_0021467 GCST90024892 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (32:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 32:1 measurement http://www.ebi.ac.uk/efo/EFO_0010373 GCST90024893 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (32:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90024894 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:0) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 33:0 measurement http://www.ebi.ac.uk/efo/EFO_0021468 GCST90024895 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:0) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 33:0 measurement http://www.ebi.ac.uk/efo/EFO_0021468 GCST90024896 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 33:1 measurement http://www.ebi.ac.uk/efo/EFO_0021469 GCST90024897 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylcholine (33:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine 33:2 measurement http://www.ebi.ac.uk/efo/EFO_0021470 GCST90024898 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024974 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024975 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024976 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024977 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024978 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024979 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024980 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024981 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024982 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:5) (n3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024983 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:5) (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024984 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024985 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024986 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024987 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_22:6) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024988 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (18:1_22:6) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024989 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (36:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024990 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (38:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024991 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (38:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024992 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024993 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024994 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024995 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024996 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-16:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024997 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024998 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/20:4) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025024 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/22:6) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025025 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/22:6) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025026 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025027 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025028 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/18:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025029 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025030 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025031 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025032 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/20:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025033 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025034 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:5) (n3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025035 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:5) (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025036 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025037 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025038 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:2) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025039 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:2) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025040 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/18:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025041 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025042 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025043 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:4) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025044 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:4) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025045 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025046 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/20:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025047 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025048 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/22:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024999 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025000 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:1/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025001 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-18:1/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025002 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-34:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025003 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-36:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025004 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-38:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025005 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylethanolamine (O-38:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025006 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025007 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/20:4) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025008 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/20:4) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025009 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/22:6) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025010 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-15:0/22:6) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025011 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025012 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025013 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/18:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025014 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025015 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025016 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025017 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/20:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025018 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025019 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:5) (n3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025020 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:5) (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025021 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-16:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025022 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-17:0/20:4) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025023 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/22:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024949 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024950 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:1/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024951 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:1/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024952 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-20:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024953 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-36:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024954 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-38:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024955 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-38:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024956 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024957 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024958 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024959 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (15-MHDA_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024960 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024961 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_16:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024962 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024963 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024964 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024965 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_18:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024966 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024967 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024968 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_20:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024969 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024970 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:1_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024971 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (16:1_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024972 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylethanolamine (17:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90024973 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-32:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024924 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024925 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024926 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-34:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024927 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-35:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024928 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-36:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024929 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-36:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024930 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-38:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024931 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024932 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:7) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024933 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkylphosphatidylcholine (O-40:7) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024934 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-15:0/20:4) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024935 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-15:0/20:4) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024936 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024937 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/16:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024938 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024939 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024940 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024941 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/18:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024942 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024943 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-16:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024944 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-17:0/20:4) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024945 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-17:0/20:4) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024946 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024947 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylcholine (P-18:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90024948 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (58:8) [NL-22:6] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90025811 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-50:1) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025812 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-52:0) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025813 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-52:2) [NL-16:0] levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025814 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Acylcarnitine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025815 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Cholesteryl ester levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025816 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Ceramide levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025817 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total free cholesterol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90025818 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dehydrocholesteryl ester levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025819 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Diacylglycerol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025820 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dihexosylceramide levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025821 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dihydroceramide levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025822 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total GM1 ganglioside levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM1 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021450 GCST90025823 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total GM3 ganglioside levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025824 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylcholine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025825 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkylphosphatidylcholine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025826 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkenylphosphatidylcholine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025827 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylethanolamine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025828 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkenylphosphatidylethanolamine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025829 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylinositol levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025830 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Monohexosylceramide levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025831 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Oxidized sterol ester levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90025832 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylcholine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025833 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkylphosphatidylcholine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025834 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkenylphosphatidylcholine levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025835 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:1) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 54:1 measurement http://www.ebi.ac.uk/efo/EFO_0010419 GCST90025174 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:2) [NL-18:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 54:2 measurement http://www.ebi.ac.uk/efo/EFO_0010420 GCST90025175 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:3) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90025176 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:4) [NL-18:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90025177 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:4) [NL-18:2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90025178 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:5) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90025179 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:6) [NL-18:2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90025180 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (56:6) [NL-20:4] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90025181 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (56:8) [NL-20:4] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90025182 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (58:8) [NL-22:6] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90025183 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-50:1) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025184 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-52:0) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025185 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkyldiacylglycerol (O-52:2) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025186 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Acylcarnitine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025187 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Cholesteryl ester levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025188 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Ceramide levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025189 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total free cholesterol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90025190 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dehydrocholesteryl ester levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90025191 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Diacylglycerol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025192 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dihexosylceramide levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025193 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Dihydroceramide levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025194 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total GM1 ganglioside levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 GM1 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021450 GCST90025195 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total GM3 ganglioside levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 GM3 ganglioside measurement http://www.ebi.ac.uk/efo/EFO_0021451 GCST90025196 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylcholine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025197 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkylphosphatidylcholine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025198 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkenylphosphatidylcholine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025199 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylethanolamine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025200 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysoalkenylphosphatidylethanolamine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025201 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Lysophosphatidylinositol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025202 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Monohexosylceramide levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025203 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylcholine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025204 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkylphosphatidylcholine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90025205 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkenylphosphatidylcholine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025206 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylethanolamine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025207 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkylphosphatidylethanolamine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025208 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkenylphosphatidylethanolamine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025209 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylglycerol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025210 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylinositol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90025211 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Phosphatidylserine levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025212 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Sphingomyelin levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025213 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Sulfatide levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025214 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Triacylglycerol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90025215 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Alkyldiacylglycerol levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90025216 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Trihexosylcermide levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025217 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Total Ubiquinone levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90025218 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ubiquinone levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90025219 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (12:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025220 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (13:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025221 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025222 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025223 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90025149 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90025150 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:0) [NL-18:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 50:0 measurement http://www.ebi.ac.uk/efo/EFO_0021480 GCST90025151 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:1) [NL-14:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90025152 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:1) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90025153 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90025154 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90025155 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:2) [NL-18:2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90025156 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-14:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90025157 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-16:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90025158 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:3) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90025159 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (50:4) [NL-14:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90025160 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:0) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 51:0 measurement http://www.ebi.ac.uk/efo/EFO_0021481 GCST90025161 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:1) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90025162 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-15:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90025163 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90025164 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (51:2) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90025165 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:1) [NL-18:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 52:1 measurement http://www.ebi.ac.uk/efo/EFO_0010413 GCST90025166 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:2) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90025167 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:3) [NL-16:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90025168 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:3) [NL-18:2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90025169 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:4) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90025170 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (52:4) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90025171 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (53:2) [NL-17:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90025172 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (54:0) [NL-18:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 54:0 measurement http://www.ebi.ac.uk/efo/EFO_0021485 GCST90025173 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/14:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025124 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025125 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/17:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025126 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025127 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025128 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025129 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025130 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/23:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025131 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:2/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025132 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d19:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025133 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 4 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025134 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/16:0(OH) levels) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025135 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025136 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:0(OH) levels) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025137 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025138 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sulfatide (d18:1/24:1(OH) levels) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025139 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:0) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90025140 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:1) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90025141 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-14:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025142 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-16:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025143 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-16:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025144 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:2) [NL-18:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90025145 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:3) [NL-16:1] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90025146 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (48:3) [NL-18:2] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90025147 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Triacylglycerol (49:1) [NL-15:0] levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90025148 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025074 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025075 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025076 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025077 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025078 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:5) (n3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025079 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:5) (n6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025080 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025081 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:1_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025082 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (20:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025083 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (34:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025084 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (36:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025085 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (37:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025086 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025087 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025088 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (38:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025089 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (39:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025090 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (36:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025091 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (36:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025092 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025093 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025094 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (38:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025095 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (40:5) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025096 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylserine (40:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90025097 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (34:3) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025098 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:5) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025049 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:5) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025050 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:6) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025051 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-18:1/22:6) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025052 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-19:0/20:4) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 5 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025053 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-19:0/20:4) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025054 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025055 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025056 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025057 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:0/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025058 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:1/20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025059 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Alkenylphosphatidylethanolamine (P-20:1/22:6) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90025060 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (34:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025061 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (34:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025062 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (36:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025063 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylglycerol (36:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025064 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_20:4) levels/Phosphatidylinositol (17:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025065 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025066 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_16:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025067 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:3) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025068 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:3) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025069 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (16:0_20:4) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025070 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_18:1) levels/Phosphatidylinositol (17:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025071 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (15-MHDA_18:2) levels/Phosphatidylinositol (17:0_18:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025072 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Phosphatidylinositol (18:0_18:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90025073 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (35:2) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025099 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (37:2) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025100 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (41:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025101 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (41:1) (a) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025102 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025103 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:2) (b) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025104 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (43:2) (c) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025105 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/19:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025106 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/23:0) levels/Sphingomyelin (d17:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025107 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d16:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025108 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/14:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025109 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025110 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d17:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025111 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/14:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025112 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025113 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:0/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025114 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/14:0) levels/Sphingomyelin (d16:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025115 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/16:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025116 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/17:0) levels/Sphingomyelin (d17:1/18:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025117 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/18:0) levels/Sphingomyelin (d16:1/20:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025118 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/20:0) levels/Sphingomyelin (d16:1/22:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025119 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/22:0) levels/Sphingomyelin (d16:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025120 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/23:0) levels/Sphingomyelin (d17:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025121 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/24:0) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025122 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Sphingomyelin (d18:1/24:1) levels 6,057 European ancestry individuals NA Illumina [14981503] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90025123 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90025249 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90025250 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0021441 GCST90025251 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0021442 GCST90025252 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021443 GCST90025253 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:5) (n3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90025254 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:5) (n6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90025255 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (22:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90025256 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021445 GCST90025257 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 24:1 measurement http://www.ebi.ac.uk/efo/EFO_0021446 GCST90025258 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:4) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 24:4 measurement http://www.ebi.ac.uk/efo/EFO_0021447 GCST90025259 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:5) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 24:5 measurement http://www.ebi.ac.uk/efo/EFO_0021448 GCST90025260 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (24:6) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 cholesteryl ester 24:6 measurement http://www.ebi.ac.uk/efo/EFO_0021449 GCST90025261 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025262 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025263 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025264 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025265 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025266 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d16:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025267 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025268 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025269 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025270 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025271 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025272 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d17:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025273 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025274 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025275 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025276 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025277 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025278 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Dihydroceramide (d18:0/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025279 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025280 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025281 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025282 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 3 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025283 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/22:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025284 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/24:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025285 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/24:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025286 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:1/26:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025287 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025288 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025289 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/17:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025290 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Ceramide (d18:2/18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90025291 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (14:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025224 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (15:0) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025225 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (15:0) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025226 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025227 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (16:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025228 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (17:0) (a) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025229 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (17:0) (b) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025230 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025231 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025232 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Acylcarnitine (18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90025233 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (14:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010340 GCST90025234 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (15:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021434 GCST90025235 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90025236 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90025237 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (16:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 16:2 measurement http://www.ebi.ac.uk/efo/EFO_0021435 GCST90025238 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (17:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021436 GCST90025239 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (17:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 17:1 measurement http://www.ebi.ac.uk/efo/EFO_0021437 GCST90025240 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90025241 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90025242 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90025243 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (18:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90025244 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:0) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 20:0 measurement http://www.ebi.ac.uk/efo/EFO_0021438 GCST90025245 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:1) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 0 cholesteryl ester 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021439 GCST90025246 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:2) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 1 cholesteryl ester 20:2 measurement http://www.ebi.ac.uk/efo/EFO_0021440 GCST90025247 Genome-wide genotyping array 2022-07-05 35668104 Cadby G 2022-06-06 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35668104 Comprehensive genetic analysis of the human lipidome identifies loci associated with lipid homeostasis with links to coronary artery disease. Cholesteryl ester (20:3) levels 4,492 European ancestry individuals 1,565 European ancestry individuals Illumina [13869437] (imputed) 2 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90025248 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Apolipoprotein B levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 66 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90092809 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. 3-Hydroxybutyrate levels 113,594 European ancestry individuals NA NR [11722792] (imputed) 20 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90092811 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Citrate levels 115,068 European ancestry individuals NA NR [11722792] (imputed) 40 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90092813 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Clinical LDL cholesterol levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 58 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092814 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Creatinine levels 110,051 European ancestry individuals NA NR [11722792] (imputed) 78 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90092815 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Docosahexaenoic acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 49 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90092816 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Glutamine levels 114,751 European ancestry individuals NA NR [11722792] (imputed) 51 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90092818 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Glucose levels 114,870 European ancestry individuals NA NR [11722792] (imputed) 24 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90092819 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Glycine levels 114,978 European ancestry individuals NA NR [11722792] (imputed) 75 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90092820 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Glycoprotein acetyls levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 72 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90092821 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. HDL cholesterol levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 107 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092822 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Histidine levels 114,897 European ancestry individuals NA NR [11722792] (imputed) 24 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90092830 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Isoleucine levels 115,079 European ancestry individuals NA NR [11722792] (imputed) 10 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90092843 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Linoleic acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 74 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90092880 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Lactate levels 114,806 European ancestry individuals NA NR [11722792] (imputed) 11 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90092882 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. LDL cholesterol levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 60 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092883 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Leucine levels 115,078 European ancestry individuals NA NR [11722792] (imputed) 20 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90092891 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 92 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092892 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phenylalanine levels 115,030 European ancestry individuals NA NR [11722792] (imputed) 13 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90092936 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Polyunsaturated fatty acid levels 115,006 European ancestry individuals NA NR [11722792] (imputed) 80 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST90092939 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Pyruvate levels 114,749 European ancestry individuals NA NR [11722792] (imputed) 26 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90092942 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total cholesterol levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 73 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90092985 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total esterified cholesterol levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 78 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90092986 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total free cholesterol levels 115,082 European ancestry individuals NA NR [11722792] (imputed) 75 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90092988 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 40 levels 1,915 individuals NA Illumina [NR] (imputed) 7 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101860 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 42 levels 1,911 individuals NA Illumina [NR] (imputed) 7 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101861 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma neurofilament light levels 1,848 individuals NA Illumina [NR] (imputed) 5 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST90101844 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma glial fibrillary acidic protein levels 1,903 individuals NA Illumina [NR] (imputed) 12 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90101845 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma p-tau181 levels 1,869 individuals NA Illumina [NR] (imputed) 7 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90101846 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 42 to 40 ratio 1,902 individuals NA Illumina [NR] (imputed) 14 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101862 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 40 levels in Alzheimer disease 1,415 individuals NA Illumina [NR] (imputed) 0 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101863 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 42 levels in Alzheimer disease 1,417 individuals NA Illumina [NR] (imputed) 2 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101864 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma neurofilament light levels in Alzheimer disease 1,394 individuals NA Illumina [NR] (imputed) 1 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST90101850 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma glial fibrillary acidic protein levels in Alzheimer disease 1,361 individuals NA Illumina [NR] (imputed) 4 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90101851 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma p-tau181 levels in Alzheimer disease 1,389 individuals NA Illumina [NR] (imputed) 1 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90101852 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 42 to 40 ratio in Alzheimer disease 1,413 individuals NA Illumina [NR] (imputed) 6 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101865 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 40 levels 492 individuals NA Illumina [NR] (imputed) 0 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101866 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 42 levels 486 individuals NA Illumina [NR] (imputed) 0 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101867 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma neurofilament light levels 501 individuals NA Illumina [NR] (imputed) 0 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST90101856 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma glial fibrillary acidic protein levels 478 individuals NA Illumina [NR] (imputed) 0 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90101857 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma p-tau181 levels 472 individuals NA Illumina [NR] (imputed) 0 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90101858 Genome-wide genotyping array 2022-04-22 35383826 Stevenson-Hoare J 2022-04-06 Brain www.ncbi.nlm.nih.gov/pubmed/35383826 Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease. Plasma amyloid beta 42 to 40 ratio 481 individuals NA Illumina [NR] (imputed) 0 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90101868 Genome-wide genotyping array 2022-05-17 27329260 Teumer A 2016-06-21 Aging Cell www.ncbi.nlm.nih.gov/pubmed/27329260 Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits. Serum levels of protein IGF1 27,520 European ancestry individuals 3,364 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 7 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90102623 Genome-wide genotyping array 2022-05-17 27329260 Teumer A 2016-06-21 Aging Cell www.ncbi.nlm.nih.gov/pubmed/27329260 Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits. Serum levels of protein IGFBP3 18,995 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 7 IGFBP-3 measurement http://www.ebi.ac.uk/efo/EFO_0004626 GCST90102624 Genome-wide genotyping array 2022-05-17 27329260 Teumer A 2016-06-21 Aging Cell www.ncbi.nlm.nih.gov/pubmed/27329260 Genomewide meta-analysis identifies loci associated with IGF-I and IGFBP-3 levels with impact on age-related traits. IGF-1 and IGFBP-3 levels (bivariate analysis) 18,995 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 10 IGF-1 measurement, IGFBP-3 measurement http://www.ebi.ac.uk/efo/EFO_0004627, http://www.ebi.ac.uk/efo/EFO_0004626 GCST90102625 Genome-wide genotyping array 2023-06-19 37311799 Hasegawa K 2023-06-13 Hum Genome Var www.ncbi.nlm.nih.gov/pubmed/37311799 Genome-wide association study of preterm birth and gestational age in a Japanese population. Gestational age at birth (maternal effect) 1,028 Japanese ancestry individuals NA Illumina [11171332] (imputed) 0 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST90268005 Genome-wide genotyping array 2023-06-19 37311799 Hasegawa K 2023-06-13 Hum Genome Var www.ncbi.nlm.nih.gov/pubmed/37311799 Genome-wide association study of preterm birth and gestational age in a Japanese population. Preterm birth (maternal effect) 384 Japanese ancestry cases, 644 Japanese ancestry controls NA Illumina [11174343] (imputed) 0 premature birth http://www.ebi.ac.uk/efo/EFO_0003917 GCST90268004 Genome-wide genotyping array 2023-12-11 37280435 Hawkes G 2023-06-06 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37280435 Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. Childhood body mass index 441,761 European ancestry individuals NA NR [NR] (imputed) 350 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90301649 Genome-wide genotyping array 2023-12-11 37280435 Hawkes G 2023-06-06 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37280435 Genetic evidence that high BMI in childhood has a protective effect on intermediate diabetes traits, including measures of insulin sensitivity and secretion, after accounting for BMI in adulthood. Body mass index 441,761 European ancestry individuals NA NR [NR] (imputed) 1150 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90301650 Genome-wide genotyping array 2023-10-31 37844115 Mocci E 2023-10-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37844115 Genome wide association joint analysis reveals 99 risk loci for pain susceptibility and pleiotropic relationships with psychiatric, metabolic, and immunological traits. Pain (pleiotropy) 361,194 European ancestry individuals NA Affymetrix [1187151] (imputed) 99 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90104572 Genome-wide genotyping array 2023-10-31 37844115 Mocci E 2023-10-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37844115 Genome wide association joint analysis reveals 99 risk loci for pain susceptibility and pleiotropic relationships with psychiatric, metabolic, and immunological traits. Pain (pleiotropy) 194,174 European ancestry individuals NA Affymetrix [1187151] (imputed) 57 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90104573 Genome-wide genotyping array 2023-10-31 37844115 Mocci E 2023-10-16 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37844115 Genome wide association joint analysis reveals 99 risk loci for pain susceptibility and pleiotropic relationships with psychiatric, metabolic, and immunological traits. Pain (pleiotropy) 167,020 European ancestry individuals NA Affymetrix [1187151] (imputed) 37 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90104574 Genome-wide genotyping array 2023-10-04 37770635 Kavousi M 2023-09-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37770635 Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. Coronary artery calcification 28,655 European ancestry individuals, 8,065 African American individuals NA Affymetrix, Illumina [8586047] (imputed) 16 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90278455 Genome-wide genotyping array 2023-10-04 37770635 Kavousi M 2023-09-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37770635 Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification. Coronary artery calcification 28,655 European ancestry individuals NA Affymetrix, Illumina [9311825] (imputed) 17 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90278456 Genome-wide genotyping array 2023-12-08 37140068 Strausz T 2023-04-26 Sleep www.ncbi.nlm.nih.gov/pubmed/37140068 Genetic analysis of probable sleep bruxism and its associations with clinical and behavioral traits. Probable sleep bruxism 12,297 Finnish ancestry cases, 364,980 Finnish ancestry controls NA Affymetrix, Illumina [20861210] (imputed) 1 bruxism http://purl.obolibrary.org/obo/MONDO_0002443 GCST90296383 Genome-wide genotyping array 2023-10-20 36870520 Chen SD 2023-03-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36870520 Genome-wide survival study identifies PARL as a novel locus for clinical progression and neurodegeneration in Alzheimer's disease. Time to Alzheimer's disease 1,158 European ancestry individuals 211,817 British ancestry individuals Illumina [1366501] (imputed) 0 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST90296100 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 12,13-dihydroxyoctadec-9-enoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 0 level of 12,13-dihydroxyoctadec-9-enoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050348 GCST90274930 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 13-hydroxyoctadecadienoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 1 level of 13-hydroxyoctadecadienoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050347 GCST90274931 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 9-hydroxylinoleic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 1 level of 9-hydroxylinoleic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050346 GCST90274932 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 9,10-dihydroxyoctadec-12-enoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 0 level of 9,10-dihydroxyoctadec-12-enoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050345 GCST90274933 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 9,10-dihydroxyoctadeca-12,15-dienoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 0 level of 9,10-dihydroxyoctadeca-12,15-dienoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050344 GCST90274934 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 11-hydroxy-arachidonic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 2 level of 11-hydroxy-arachidonic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050343 GCST90274935 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 5-hydroxy-6,8,11,14-eicosatetraenoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 0 level of 5-hydroxy-6,8,11,14-eicosatetraenoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050342 GCST90274936 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 12-hydroxy-5,8,10,14-eicosatetraenoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 0 level of 12-hydroxy-5,8,10,14-eicosatetraenoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050341 GCST90274937 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 11,12-dihydroxyicosa-5,8,14-trienoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 0 level of 11,12-dihydroxyicosa-5,8,14-trienoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050340 GCST90274938 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin 14,15-dihydroxyeicosa-5,8,11-trienoic acid levels 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 0 level of 14,15-dihydroxyeicosa-5,8,11-trienoic acid in blood plasma http://purl.obolibrary.org/obo/OBA_2050339 GCST90274939 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin levels (PC2) 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 2 level of oxylipin in blood plasma http://purl.obolibrary.org/obo/OBA_2050338 GCST90274940 Genome-wide genotyping array 2023-10-11 37057071 Buckner T 2023-03-28 Front Nutr www.ncbi.nlm.nih.gov/pubmed/37057071 Genome-wide analysis of oxylipins and oxylipin profiles in a pediatric population. Plasma oxylipin levels (PC1) 253 European ancestry children at risk of type 1 diabetes, 63 children at risk of type 1 diabetes NA Illumina [6196887] (imputed) 2 level of oxylipin in blood plasma http://purl.obolibrary.org/obo/OBA_2050338 GCST90274941 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (Fla) 158 European ancestry individuals NA Illumina [6217943] (imputed) 4 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093075 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (LPA) 240 European ancestry individuals NA Illumina [6217943] (imputed) 2 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093076 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (LTA) 145 European ancestry individuals NA Illumina [6217943] (imputed) 3 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093077 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (Hin) 268 European ancestry individuals NA Illumina [6217943] (imputed) 1 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093078 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (PAM) 202 European ancestry individuals NA Illumina [6217943] (imputed) 0 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093079 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (PGN) 189 European ancestry individuals NA Illumina [6217943] (imputed) 0 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093080 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (Strpn) 266 European ancestry individuals NA Illumina [6217943] (imputed) 0 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093081 Genome-wide genotyping array 2023-10-05 35931775 Lin L 2022-08-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35931775 A systems immunology approach to investigate cytokine responses to viruses and bacteria and their association with disease. IL-6 response to bacterial stimulus (FSL) 177 European ancestry individuals NA Illumina [6217943] (imputed) 0 interleukin-6 measurement, response to stimulus http://www.ebi.ac.uk/efo/EFO_0004810, http://purl.obolibrary.org/obo/GO_0050896 GCST90093074 Genome-wide genotyping array 2023-12-06 33848412 Lee JW 2021-04-12 Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/33848412 Absolute Neutrophil Count after the First Chemotherapy Cycle as a Surrogate Marker for Treatment Outcomes in Patients with Neuroblastoma. Absolute neutrophil count 313 individuals NA Illumina 29 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90038455 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (fetal genotype, adjusted for sex and gestational age) 65,405 European ancestry individuals NA NR [13311132] (imputed) 36 fetal genotype effect measurement, body weights and measures http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0004324 GCST90275189 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (maternal genotype, adjusted for sex and gestational age) 61,228 European ancestry individuals NA NR [14930692] (imputed) 8 body weights and measures, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004324, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90275190 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (paternal genotype, adjusted for sex and gestational age) 52,392 European ancestry individuals NA NR [13849987] (imputed) 5 body weights and measures, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004324, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90275191 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (fetal effect, conditional on maternal and paternal genotype) 65,405 European ancestry individuals NA NR [11749766] (imputed) 0 fetal genotype effect measurement, body weights and measures http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0004324 GCST90275192 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (maternal effect, conditional on fetal and paternal genotype) 61,228 European ancestry individuals NA NR [11749766] (imputed) 0 body weights and measures, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004324, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90275193 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (paternal effect, conditional on fetal and maternal genotype) 52,392 European ancestry individuals NA NR [11749766] (imputed) 0 body weights and measures, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004324, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90275194 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (fetal effect, conditional on maternal genotype) 65,405 European ancestry individuals NA NR [11749766] (imputed) 0 fetal genotype effect measurement, body weights and measures http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0004324 GCST90275195 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (maternal effect, conditional on fetal genotype) 61,228 European ancestry individuals NA NR [11749766] (imputed) 0 body weights and measures, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004324, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90275196 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (fetal genotype, adjusted for sex) 65,651 European ancestry individuals NA NR [13328667] (imputed) 39 fetal genotype effect measurement, body weights and measures http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0004324 GCST90275197 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (maternal genotype, adjusted for sex) 61,241 European ancestry individuals NA NR [14930167] (imputed) 4 body weights and measures, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004324, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90275198 Genome-wide genotyping array 2023-10-23 37798380 Beaumont RN 2023-10-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37798380 Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth. Placental weight (paternal genotype, adjusted for sex) 52,402 European ancestry individuals NA NR [13851099] (imputed) 2 body weights and measures, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004324, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90275199 Genome-wide genotyping array 2023-11-03 37170954 Yang X 2023-05-12 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/37170954 Genotype-Phenotype Models Predicting VO2max Response to High-Intensity Interval Training in Physically Inactive Chinese. Response to high-intensity interval training in physically inactive (maximal oxygen uptake) 228 Chinese ancestry individuals NA Illumina [NR] (imputed) 10 maximal oxygen uptake measurement, response to exercise http://www.ebi.ac.uk/efo/EFO_0004887, http://www.ebi.ac.uk/efo/EFO_0007768 GCST90296672 Genome-wide genotyping array 2023-10-05 37188768 Villaplana-Velasco A 2023-05-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37188768 Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes. Retinal vascular fractal dimension (right eye) 38,811 British ancestry individuals 4,288 European ancestry individuals, 568 Asian ancestry individuals, 509 African ancestry individuals NR [9275849] (imputed) 0 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90293087 Genome-wide genotyping array 2023-10-05 37188768 Villaplana-Velasco A 2023-05-15 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37188768 Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes. Retinal vascular fractal dimension (left eye) 38,017 British ancestry individuals 4,340 European ancestry individuals, 562 Asian ancestry individuals, 498 African ancestry individuals NR [9275849] (imputed) 0 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90293088 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Arthritis 268 Hispanic or Latin American cases, 5,453 Hispanic or Latin American controls NA Illumina [28315198] 1 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90296592 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. BMI 5,642 Hispanic or Latin American individuals NA Illumina [28126162] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90296593 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Cholesterol levels 4,484 Hispanic or Latin American individuals NA Illumina [25423662] 4 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90296594 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Creatinine levels 4,482 Hispanic or Latin American individuals NA Illumina [25614082] 1 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90296595 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Diastolic blood pressure (adjusted for treatment) 5,737 Hispanic or Latin American individuals NA Illumina [28122199] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90296596 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Diastolic blood pressure 5,737 Hispanic or Latin American individuals NA Illumina [28122199] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90296597 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Diabetes 291 Hispanic or Latin American cases, 5,443 Hispanic or Latin American controls NA Illumina [28343717] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90296598 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Fasting glucose 1,361 Hispanic or Latin American individuals NA Illumina [15727593] 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90296599 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Glucose levels 4,418 Hispanic or Latin American individuals NA Illumina [25454794] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90296600 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Gout 156 Hispanic or Latin American cases, 5,566 Hispanic or Latin American controls NA Illumina [28318280] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90296601 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. HDL cholesterol levels 4,484 Hispanic or Latin American individuals NA Illumina [25423662] 10 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90296602 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Height 5,663 Hispanic or Latin American individuals NA Illumina [28176604] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90296603 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. High cholesterol 345 Hispanic or Latin American cases, 5,363 Hispanic or Latin American controls NA Illumina [28289845] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90296604 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Hypertension 1 748 Hispanic or Latin American cases, 4,035 Hispanic or Latin American controls NA Illumina [26044813] 1 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90296605 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Hypertension 2 1,839 Hispanic or Latin American cases, 3,200 Hispanic or Latin American controls NA Illumina [26622218] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90296606 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. LDL cholesterol levels 4,453 Hispanic or Latin American individuals NA Illumina [25350180] 3 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90296607 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Rheumatoid arthritis 502 Hispanic or Latin American cases, 5,515 Hispanic or Latin American controls NA Illumina [28312801] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90296608 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Systolic blood pressure (adjusted for treatment) 5,737 Hispanic or Latin American individuals NA Illumina [28122199] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90296609 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Systolic blood pressure 5,737 Hispanic or Latin American individuals NA Illumina [28122199] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90296610 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Triglyceride levels 4,483 Hispanic or Latin American individuals NA Illumina [25420360] 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90296611 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Inflammatory disease 677 Hispanic or Latin American cases, 5,046 Hispanic or Latin American controls NA Illumina [28323180] 0 inflammatory disease http://www.ebi.ac.uk/efo/EFO_0009903 GCST90296612 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Weight 5,681 Hispanic or Latin American individuals NA Illumina [28212325] 1 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90296613 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Arthritis up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9469207] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90296614 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. BMI up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9435909] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90296615 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Cholesterol levels up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8398870] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90296616 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Creatinine levels up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8433479] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90296617 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Diastolic blood pressure (adjusted for treatment) up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9433053] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90296618 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Diastolic blood pressure up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9433053] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90296619 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Diabetes up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9481233] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90296620 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Fasting glucose up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [6194469] 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90296621 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Glucose levels up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8387769] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90296622 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Gout up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9469207] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90296623 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. HDL cholesterol levels up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8398870] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90296624 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Height up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9446501] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90296625 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. High cholesterol up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9462649] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90296626 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Hypertension 1 up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8578013] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90296627 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Hypertension 2 up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8771894] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90296628 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. LDL cholesterol levels up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8372090] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90296629 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Rheumatoid arthritis up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9469208] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90296630 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Systolic blood pressure (adjusted for treatment) up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9433053] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90296631 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Systolic blood pressure up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9433053] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90296632 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Triglyceride levels up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [8398870] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90296633 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Inflammatory disease up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9469209] 0 inflammatory disease http://www.ebi.ac.uk/efo/EFO_0009903 GCST90296634 Genome-wide genotyping array 2023-11-01 37821706 Sohail M 2023-10-11 Nature www.ncbi.nlm.nih.gov/pubmed/37821706 Mexican Biobank advances population and medical genomics of diverse ancestries. Weight up to 1,061 Hispanic or Latin American individuals (with >90% Native American ancestry) NA Illumina [9462748] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90296635 Genome-wide genotyping array 2023-10-23 36973108 Nodari Y 2023-03-25 Dig Liver Dis www.ncbi.nlm.nih.gov/pubmed/36973108 Genetic and non-genetic risk factors for early-onset pancreatic cancer. Early-onset pancreatic cancer 603 cases, 6,897 controls 309 European, East Asian, Hispanic/Latino or unknown ancestry cases, 3,325 European, East Asian, Hispanic/Latino or unknown ancestry controls NR [6993629] (imputed) 0 pancreatic ductal adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0002517 GCST90296102 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Concurrent manic symptoms in manic depressive disorder and/or anxiety disorders (sum score) 11,568 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296673 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Concurrent manic symptoms in manic depressive disorder and/or anxiety disorders (energy or activity factor) 11,568 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296674 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Concurrent manic symptoms in manic depressive disorder and/or anxiety disorders (cognitive factor) 11,568 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296675 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Concurrent manic symptoms in manic depressive disorder and/or anxiety disorders (impulsivity factor) 11,568 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296676 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Lifetime manic symptoms in manic depressive disorder and/or anxiety disorders (sum score) 19,859 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296677 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Lifetime manic symptoms in manic depressive disorder and/or anxiety disorders (energy or activity factor) 19,859 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296678 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Lifetime manic symptoms in manic depressive disorder and/or anxiety disorders (cognitive factor) 19,859 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296679 Genome-wide genotyping array 2023-11-03 37178379 Mundy J 2023-05-13 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37178379 Genetic examination of the Mood Disorder Questionnaire and its relationship with bipolar disorder. Lifetime manic symptoms in manic depressive disorder and/or anxiety disorders (impulsivity factor) 19,859 European ancestry individuals NA Affymetrix [NR] (imputed) 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90296680 Genome-wide genotyping array 2023-10-26 37358671 Lin S 2023-06-26 Eur J Epidemiol www.ncbi.nlm.nih.gov/pubmed/37358671 Genome-wide epistasis study highlights genetic interactions influencing severity of COVID-19. Severe COVID-19 infection 2,243 British ancestry cases, 12,612 British ancestry controls NA Affymetrix [7873610] (imputed) 5 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296442 Genome-wide genotyping array 2023-10-20 37784116 Ruth KS 2023-10-02 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/37784116 Insights into the genetics of menopausal vasomotor symptoms: genome-wide analyses of routinely-collected primary care health records. Menopausal vasomotor symptoms 14,261 European ancestry cases, 77,767 European ancestry controls NA NR [17091110] (imputed) 1 menopause http://www.ebi.ac.uk/efo/EFO_0003922 GCST90267381 Genome-wide genotyping array 2023-10-23 36927043 Chakraborty S 2023-03-17 Eur J Ophthalmol www.ncbi.nlm.nih.gov/pubmed/36927043 A quantitative trait GWAS on lens thickness identifies novel risk loci on PTPRM in the narrow angle individuals susceptible to PACG. Lens thickness in narrow iridocorneal angle 240 Indian ancestry individuals 89 individuals Illumina [11907545] (imputed) 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90296101 Genome-wide genotyping array 2023-10-27 37156939 Xu H 2023-05-08 Addiction www.ncbi.nlm.nih.gov/pubmed/37156939 Identifying Genetic Loci and Phenomic Associations of Substance Use Traits: A Multi-trait Analysis of GWAS (MTAG) study. Opioid use disorder (MTAG) 74,635 European ancestry individuals (MTAG effective sample size boosted by cannabis use disorder, alcohol use disorder, smoking samples) NA NR [2888846] 41 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90296425 Genome-wide genotyping array 2023-10-27 37156939 Xu H 2023-05-08 Addiction www.ncbi.nlm.nih.gov/pubmed/37156939 Identifying Genetic Loci and Phenomic Associations of Substance Use Traits: A Multi-trait Analysis of GWAS (MTAG) study. Opioid use disorder (MTAG) 32,240 African ancestry individuals (MTAG effective sample size boosted by cannabis use disorder, alcohol use disorder, smoking samples) NA NR [2648505] 2 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90296426 Genome-wide genotyping array 2023-10-27 37156939 Xu H 2023-05-08 Addiction www.ncbi.nlm.nih.gov/pubmed/37156939 Identifying Genetic Loci and Phenomic Associations of Substance Use Traits: A Multi-trait Analysis of GWAS (MTAG) study. Cannabis use disorder (MTAG) 48,900 European ancestry individuals (MTAG effective sample size boosted by opioid use disorder, alcohol use disorder, smoking samples) NA NR [2888846] 74 cannabis dependence http://www.ebi.ac.uk/efo/EFO_0007191 GCST90296427 Genome-wide genotyping array 2023-10-27 37156939 Xu H 2023-05-08 Addiction www.ncbi.nlm.nih.gov/pubmed/37156939 Identifying Genetic Loci and Phenomic Associations of Substance Use Traits: A Multi-trait Analysis of GWAS (MTAG) study. Alcohol use disorder (MTAG) 171,601 European ancestry individuals (MTAG effective sample size boosted by opioid use disorder, cannabis use disorder, smoking samples) NA NR [2888846] 63 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90296428 Genome-wide genotyping array 2023-10-27 37156939 Xu H 2023-05-08 Addiction www.ncbi.nlm.nih.gov/pubmed/37156939 Identifying Genetic Loci and Phenomic Associations of Substance Use Traits: A Multi-trait Analysis of GWAS (MTAG) study. Alcohol use disorder (MTAG) 67,686 African ancestry individuals (MTAG effective sample size boosted by opioid use disorder, cannabis use disorder, smoking samples) NA NR [2648505] 3 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90296429 Genome-wide genotyping array 2023-10-27 37156939 Xu H 2023-05-08 Addiction www.ncbi.nlm.nih.gov/pubmed/37156939 Identifying Genetic Loci and Phenomic Associations of Substance Use Traits: A Multi-trait Analysis of GWAS (MTAG) study. Smoking initiation (MTAG) 632,802 European ancestry individuals (MTAG effective sample size boosted by opioid use disorder, cannabis use disorder, alcohol use disorder samples) NA NR [2888846] 183 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST90296430 Genome-wide genotyping array 2023-10-27 37156939 Xu H 2023-05-08 Addiction www.ncbi.nlm.nih.gov/pubmed/37156939 Identifying Genetic Loci and Phenomic Associations of Substance Use Traits: A Multi-trait Analysis of GWAS (MTAG) study. Smoking trajectory (MTAG) 40,736 African ancestry individuals (MTAG effective sample size boosted by opioid use disorder, cannabis use disorder, alcohol use disorder samples) NA NR [2648505] 1 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90296431 Genome-wide genotyping array 2023-10-26 37794016 Budu-Aggrey A 2023-10-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37794016 European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Atopic dermatitis 60,653 European ancestry cases, 804,329 European ancestry controls, 368 Latino cases, 3,976 Latino controls, 863 mixed ancestry cases, 1,273 mixed ancestry controls, 2,385 Japanese ancestry cases, 209,651 Japanese ancestry controls, 838 African American cases, 2,058 African American controls 387,407 European ancestry cases, 2,517,257 European ancestry controls, 25,813 African ancestry cases, 148,202 African ancestry controls, 58,909 Latino cases, 466,439 Latino controls NR [8684278] (imputed) 7 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90244788 Genome-wide genotyping array, Exome genotyping array 2023-10-26 37794016 Budu-Aggrey A 2023-10-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37794016 European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Atopic dermatitis 60,653 European ancestry cases, 804,329 European ancestry controls 387,407 European ancestry cases, 2,517,257 European ancestry controls NR [12147822] (imputed) 81 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90244787 Genome-wide genotyping array, Exome genotyping array 2023-10-20 33462486 Atkinson EG 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462486 Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. Total cholesterol levels (joint analysis model with African background) 4,309 admixed African European ancestry individuals NA Affymetrix [7715969] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90012868 Genome-wide genotyping array 2023-10-20 33462486 Atkinson EG 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462486 Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. Total cholesterol levels (joint analysis model with European background) 4,309 admixed African European ancestry individuals NA Affymetrix [7715969] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90012869 Genome-wide genotyping array 2023-10-20 33462486 Atkinson EG 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462486 Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. Total cholesterol levels 4,309 admixed African European ancestry individuals NA Affymetrix [7800773] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90012870 Genome-wide genotyping array 2023-10-20 33462486 Atkinson EG 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462486 Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. LDL cholesterol levels (specific analysis model with African background) 2,831 admixed African European ancestry individuals NA Affymetrix [7800869] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90012871 Genome-wide genotyping array 2023-10-20 33462486 Atkinson EG 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462486 Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. LDL cholesterol levels (specific analysis model with European background) 1,486 admixed African European ancestry individuals NA Affymetrix [7800869] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90012872 Genome-wide genotyping array 2023-10-20 33462486 Atkinson EG 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462486 Tractor uses local ancestry to enable the inclusion of admixed individuals in GWAS and to boost power. LDL cholesterol levels 4,317 admixed African European ancestry individuals NA Affymetrix [7800869] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90012873 Genome-wide genotyping array 2021-03-22 33350037 Cheng CF 2020-12-22 J Gene Med www.ncbi.nlm.nih.gov/pubmed/33350037 Genetic Risk Score Constructed from Common Genetic Variants is Associated with Cardiovascular Disease Risk in Type 2 Diabetes Mellitus. Cardiovascular disease in type 2 diabetes 326 Han Chinese ancestry cases, 1,209 Han Chinese ancestry controls 68 Han Chinese ancestry cases, 317 Han Chinese ancestry controls Affymetrix, Illumina [NR] (imputed) 3 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST011371 Genome-wide genotyping array 2018-09-19 29855589 Chernus J 2018-05-31 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29855589 GWAS reveals loci associated with velopharyngeal dysfunction. Velopharyngeal dysfunction 54 Hispanic or Latin American and unknown ancestry cases, 922 Hispanic or Latin American and unknown ancestry controls NA Illumina [at least 269494] (imputed) 89 velopharyngeal dysfunction http://www.ebi.ac.uk/efo/EFO_0009336 GCST006280 Genome-wide genotyping array 2021-08-13 33649051 Duchen D 2021-03-01 Infect Immun www.ncbi.nlm.nih.gov/pubmed/33649051 Host genome wide association study of infant susceptibility to Shigella-associated diarrhea. Shigella-associated diarrhea 143 Bangladeshi cases, 446 Bangladeshi controls NA Illumina [5729117] (imputed) 12 shigellosis http://www.ebi.ac.uk/efo/EFO_0005585 GCST012207 Genome-wide genotyping array 2021-01-09 32989287 Cuellar-Partida G 2020-09-28 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32989287 Genome-wide association study identifies 48 common genetic variants associated with handedness. Ambidextrousness 47,637 European ancestry cases, 1,422,823 European ancestry controls NA Illumina [12493443] (imputed) 7 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST90013420 Genome-wide genotyping array 2021-01-09 32989287 Cuellar-Partida G 2020-09-28 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32989287 Genome-wide association study identifies 48 common genetic variants associated with handedness. Left-handedness 1,766,671 European ancestry individuals NA Illumina [12493444] (imputed) 41 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST90013421 Genome-wide genotyping array 2019-01-18 30552067 Shrine N 2018-12-11 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/30552067 Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study. Asthma (moderate or severe) 5,135 European ancestry cases, 25,675 European ancestry controls 5,414 European ancestry cases, 21,471 European ancestry controls Affymetrix [33771858] (imputed) 27 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST006911 Genome-wide genotyping array 2021-01-29 33199917 Bakker MK 2020-11-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33199917 Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Intracranial aneurysm 7,495 European ancestry cases, 71,934 European ancestry controls NA Affymetrix, Illumina [4471083] (imputed) 11 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST011020 Genome-wide genotyping array 2021-01-29 33199917 Bakker MK 2020-11-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33199917 Genome-wide association study of intracranial aneurysms identifies 17 risk loci and genetic overlap with clinical risk factors. Intracranial aneurysm 7,495 European ancestry cases, 3,259 East Asian ancestry cases, 71,934 European ancestry controls, 234,948 East Asian ancestry controls NA Affymetrix, Illumina [3527309] (imputed) 17 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST011021 Genome-wide genotyping array 2019-06-26 29459680 Claes P 2018-02-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29459680 Genome-wide mapping of global-to-local genetic effects on human facial shape. Facial morphology traits (63 three-dimensional facial segments) 2,329 European ancestry individuals 1,719 European ancestry individuals Illumina [9478608] (imputed) 10 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST007989 Genome-wide genotyping array 2021-06-18 32804141 Wang RZ 2020-08-10 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/32804141 Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging. Cerebral glucose metabolic decline (left angular gyrus) 67 European ancestry Alzheimer's disease cases, 323 European ancestry mild cognitive impairment cases, 196 European ancestry individuals with normal cognition NA Illumina [278989] 1 glucose metabolism decline measurement http://www.ebi.ac.uk/efo/EFO_0009392 GCST90010428 Genome-wide genotyping array 2021-06-18 32804141 Wang RZ 2020-08-10 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/32804141 Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging. Cerebral glucose metabolic decline (right temporal gyrus) 67 European ancestry Alzheimer's disease cases, 323 European ancestry mild cognitive impairment cases, 196 European ancestry individuals with normal cognition NA Illumina [278989] 1 glucose metabolism decline measurement http://www.ebi.ac.uk/efo/EFO_0009392 GCST90010429 Genome-wide genotyping array 2021-06-18 32804141 Wang RZ 2020-08-10 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/32804141 Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging. Cerebral glucose metabolic decline (left temporal gyrus) 67 European ancestry Alzheimer's disease cases, 323 European ancestry mild cognitive impairment cases, 196 European ancestry individuals with normal cognition NA Illumina [278989] 1 glucose metabolism decline measurement http://www.ebi.ac.uk/efo/EFO_0009392 GCST90010430 Genome-wide genotyping array 2021-06-18 32804141 Wang RZ 2020-08-10 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/32804141 Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging. Cerebral glucose metabolic decline (right angular gyrus) 67 European ancestry Alzheimer's disease cases, 323 European ancestry mild cognitive impairment cases, 196 European ancestry individuals with normal cognition NA Illumina [278989] 1 glucose metabolism decline measurement http://www.ebi.ac.uk/efo/EFO_0009392 GCST90010431 Genome-wide genotyping array 2021-06-18 32804141 Wang RZ 2020-08-10 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/32804141 Genome-Wide Association Study of Brain Alzheimer's Disease-Related Metabolic Decline as Measured by [18F] FDG-PET Imaging. Cerebral glucose metabolic decline (posterior cingulate cortex) 67 European ancestry Alzheimer's disease cases, 323 European ancestry mild cognitive impairment cases, 196 European ancestry individuals with normal cognition NA Illumina [278989] 1 glucose metabolism decline measurement http://www.ebi.ac.uk/efo/EFO_0009392 GCST90010432 Genome-wide genotyping array 2022-05-27 35181757 Wendt FR 2022-02-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35181757 Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder. Generalized anxiety disorder (mental health questionnaire or predicted) 489,579 European ancestry individuals NA Affymetrix [NR] (imputed) 10 generalized anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001892 GCST90103928 Genome-wide genotyping array 2022-05-27 35181757 Wendt FR 2022-02-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35181757 Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder. Post-traumatic stress disorder (mental health questionnaire or predicted) 497,803 European ancestry individuals NA Affymetrix [NR] (imputed) 32 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90103929 Genome-wide genotyping array 2022-05-27 35181757 Wendt FR 2022-02-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35181757 Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder. Generalized anxiety disorder (phenotype risk score) 489,579 European ancestry individuals NA Affymetrix [NR] (imputed) 12 generalized anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001892 GCST90103930 Genome-wide genotyping array 2022-05-27 35181757 Wendt FR 2022-02-18 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35181757 Using phenotype risk scores to enhance gene discovery for generalized anxiety disorder and posttraumatic stress disorder. Post-traumatic stress disorder (phenotype risk score) 497,803 European ancestry individuals NA Affymetrix [NR] (imputed) 26 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90103931 Genome-wide genotyping array 2021-07-30 33510140 Lin WY 2021-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33510140 Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia. Chronic lymphocytic leukemia (time to first treatment) 755 European ancestry individuals 87 individuals Illumina [5199911] (imputed) 2 progression free survival, chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0004920, http://www.ebi.ac.uk/efo/EFO_0000095 GCST012155 Genome-wide genotyping array 2021-08-24 33692100 Simcoe M 2021-03-10 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33692100 Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color. Eye color 157,485 European ancestry individuals 35,501 European ancestry individuals, 959 Han Chinese ancestry individuals, 677 Indian ancestry individuals Illumina [11532091] (imputed) 26 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST012219 Genome-wide genotyping array 2021-02-18 33510174 Jones G 2021-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33510174 Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. Low hand grip strength (60 years and older) (EWGSOP) 48,596 European ancestry cases, 207,927 European ancestry controls NA Affymetrix, Illumina [9457422] (imputed) 15 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90007526 Genome-wide genotyping array 2021-02-18 33510174 Jones G 2021-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33510174 Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. Low hand grip strength (60 years and older) (EWGSOP) 34,589 European ancestry female cases, 100,879 European ancestry female controls NA Affymetrix, Illumina [9449805] (imputed) 8 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90007527 Genome-wide genotyping array 2021-02-18 33510174 Jones G 2021-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33510174 Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. Low hand grip strength (60 years and older) (EWGSOP) 14,007 European ancestry male cases, 107,048 European ancestry male controls NA Affymetrix, Illumina [9464541] (imputed) 3 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90007528 Genome-wide genotyping array 2021-02-18 33510174 Jones G 2021-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33510174 Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. Low hand grip strength (60 years and older) (FNIH) 20,335 European ancestry cases, 236,188 European ancestry controls NA Affymetrix, Illumina [9465622] (imputed) 5 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90007529 Genome-wide genotyping array 2021-02-18 33510174 Jones G 2021-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33510174 Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. Low hand grip strength (60 years and older) (FNIH) 13,601 European ancestry female cases, 121,867 European ancestry female controls NA Affymetrix, Illumina [9431325] (imputed) 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90007530 Genome-wide genotyping array 2021-02-18 33510174 Jones G 2021-01-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33510174 Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women. Low hand grip strength (60 years and older) (FNIH) 6,734 European ancestry male cases, 114,321 European ancestry male controls NA Affymetrix, Illumina [9471905] (imputed) 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90007531 Genome-wide genotyping array 2021-08-13 33669428 Franco LAM 2021-02-16 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/33669428 Pharmacogenomic Profile and Adverse Drug Reactions in a Prospective Therapeutic Cohort of Chagas Disease Patients Treated with Benznidazole. Adverse response to benznidazole in Chagas disease 61 Hispanic/Latino or unknown ancestry cases, 29 Hispanic/Latino or unknown ancestry controls NA Affymetrix [at least 811691] (imputed) 12 response to benznidazole http://www.ebi.ac.uk/efo/EFO_0600031 GCST012184 Genome-wide genotyping array 2021-03-22 33558538 Gebresilase T 2021-02-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33558538 Replication of HLA class II locus association with susceptibility to podoconiosis in three Ethiopian ethnic groups. Podoconiosis 1,137 Ethiopian ancestry cases, 1,152 Ethiopian ancestry controls NA Illumina [2201695] 3 podoconiosis http://www.ebi.ac.uk/efo/EFO_0004712 GCST011363 Genome-wide genotyping array 2020-01-29 31872054 Wei L 2019-11-08 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/31872054 Identification of TYW3/CRYZ and FGD4 as susceptibility genes for amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 666 Han Chinese ancestry cases, 3,988 Han Chinese ancestry controls up to 884 Han Chinese ancestry cases, up to 5,329 Han Chinese ancestry controls Illumina [456414] 7 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST009529 Genome-wide genotyping array 2020-02-18 31872073 Hosoda Y 2019-12-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/31872073 Genome-wide association analyses identify two susceptibility loci for pachychoroid disease central serous chorioretinopathy. Central serous retinopathy 610 Japanese ancestry cases, 2,850 Japanese ancestry controls 415 Japanese ancestry cases, 6,602 Japanese ancestry controls, 521 European ancestry cases, 3,577 European ancestry controls Illumina [2893743] (imputed) 4 central serous retinopathy http://www.ebi.ac.uk/efo/EFO_0009784 GCST009653 Genome-wide genotyping array 2019-05-22 31059154 Chen Z 2019-05-06 Mov Disord www.ncbi.nlm.nih.gov/pubmed/31059154 Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy. Progressive supranuclear palsy 283 European ancestry cases, 4,472 European ancestry controls 1,178 cases, 3,759 controls Illumina [at least 284674] 1 progressive supranuclear palsy http://purl.obolibrary.org/obo/MONDO_0019037 GCST007845 Genome-wide genotyping array 2021-08-04 33562295 Coltell O 2021-02-07 Nutrients www.ncbi.nlm.nih.gov/pubmed/33562295 Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. Adiponectin levels 348 European ancestry high cardiovascular risk elderly men NA Illumina [625127] 9 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST012167 Genome-wide genotyping array 2021-08-04 33562295 Coltell O 2021-02-07 Nutrients www.ncbi.nlm.nih.gov/pubmed/33562295 Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. Adiponectin levels 606 European ancestry high cardiovascular risk elderly women NA Illumina [625127] 8 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST012166 Genome-wide genotyping array 2021-08-04 33562295 Coltell O 2021-02-07 Nutrients www.ncbi.nlm.nih.gov/pubmed/33562295 Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. Adiponectin levels in type 2 diabetes 450 European ancestry high cardiovascular risk elderly individuals NA Illumina [625127] (imputed) 1 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST012165 Genome-wide genotyping array 2021-08-04 33562295 Coltell O 2021-02-07 Nutrients www.ncbi.nlm.nih.gov/pubmed/33562295 Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. Adiponectin levels 504 European ancestry high cardiovascular risk non-diabetic elderly individuals NA Illumina [625127] 4 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST012164 Genome-wide genotyping array 2021-08-04 33562295 Coltell O 2021-02-07 Nutrients www.ncbi.nlm.nih.gov/pubmed/33562295 Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. Adiponectin levels x Mediterranean diet adherence interaction 954 European ancestry high cardiovascular risk elderly individuals NA Illumina [625127] 7 diet measurement, adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0008111, http://www.ebi.ac.uk/efo/EFO_0004502 GCST012163 Genome-wide genotyping array 2021-08-04 33562295 Coltell O 2021-02-07 Nutrients www.ncbi.nlm.nih.gov/pubmed/33562295 Circulating Adiponectin and Its Association with Metabolic Traits and Type 2 Diabetes: Gene-Diet Interactions Focusing on Selected Gene Variants and at the Genome-Wide Level in High-Cardiovascular Risk Mediterranean Subjects. Adiponectin levels 954 European ancestry high cardiovascular risk elderly individuals NA Illumina [625127] 8 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST012168 Genome-wide genotyping array 2020-04-20 31978080 Andersen MK 2020-01-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/31978080 The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders. Body mass index 4,626 Greenlandic individuals 1,529 Greenlandic individuals, 1,058 Yup’ik Alaska Native ancestry individuals Illumina [115182] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009889 Genome-wide genotyping array 2021-10-13 33676726 Ahlstrom S 2021-03-03 Br J Anaesth www.ncbi.nlm.nih.gov/pubmed/33676726 First genome-wide association study on rocuronium dose requirements shows association with SLCO1A2. Rocuronium dose requirement in breast cancer surgery 918 European ancestry individuals NA Illumina [653034] 2 response to neuromuscular blocker http://www.ebi.ac.uk/efo/EFO_0600034 GCST012479 Genome-wide genotyping array 2020-07-07 31972866 Nagel M 2020-01-23 Acta Psychiatr Scand www.ncbi.nlm.nih.gov/pubmed/31972866 Genome-wide association study of the sensitivity to environmental stress and adversity (SESA) neuroticism cluster. Sensitivity to environmental stress and adversity 351,827 European ancestry individuals NA NR [7259579] 47 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST010123 Genome-wide genotyping array 2020-09-07 32460577 Song L 2020-05-28 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/32460577 Association of TIM-1 (T-Cell Immunoglobulin and Mucin Domain 1) With Incidence of Stroke. T-Cell Immunoglobulin and Mucin domain 1 levels 4,505 European ancestry individuals NA Illumina [7328171] (imputed) 8 T-cell immunoglobulin and mucin domain 1 measurement http://www.ebi.ac.uk/efo/EFO_0010812 GCST010500 Genome-wide genotyping array 2020-04-17 29905830 Lee HS 2018-08-01 J Crohns Colitis www.ncbi.nlm.nih.gov/pubmed/29905830 An Intergenic Variant rs9268877 Between HLA-DRA and HLA-DRB Contributes to the Clinical Course and Long-term Outcome of Ulcerative Colitis. Poor prognosis in Crohn's disease 243 Korean ancestry poor prognosis cases, 364 Korean ancestry good prognosis controls 145 Korean ancestry poor prognosis cases, 129 Korean ancestry good prognosis controls Illumina [up to 519662] 1 disease prognosis measurement http://www.ebi.ac.uk/efo/EFO_0007936 GCST009878 Targeted genotyping array [ImmunoChip] 2022-05-27 35170024 Mullan KA 2022-02-16 Epilepsia www.ncbi.nlm.nih.gov/pubmed/35170024 Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications. Aromatic antiseizure medication-induced Stevens-Johnson syndrome or toxic epidermal necrolysis 113 Han Chinese ancestry cases, 84 Han Chinese ancestry controls NA Illumina [6198332] 9 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to anticonvulsant http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://purl.obolibrary.org/obo/GO_0036277 GCST90103802 Genome-wide sequencing 2022-05-27 35170024 Mullan KA 2022-02-16 Epilepsia www.ncbi.nlm.nih.gov/pubmed/35170024 Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications. Carbamazepine-induced Stevens-Johnson syndrome or toxic epidermal necrolysis (SJS/TEN) 85 Han Chinese ancestry cases, 77 Han Chinese ancestry controls NA Illumina [6198332] 1 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://www.ebi.ac.uk/efo/EFO_0008484 GCST90103803 Genome-wide sequencing 2022-05-27 35170024 Mullan KA 2022-02-16 Epilepsia www.ncbi.nlm.nih.gov/pubmed/35170024 Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications. Aromatic antiseizure medication-induced Stevens-Johnson syndrome or toxic epidermal necrolysis in HLA-B*15:02 non-carriers 35 Han Chinese ancestry cases, 53 Han Chinese ancestry controls NA Illumina [6198332] 8 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to anticonvulsant http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://purl.obolibrary.org/obo/GO_0036277 GCST90103804 Genome-wide sequencing 2021-05-14 33661925 Quistrebert J 2021-03-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33661925 Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations. Resistance to Mycobacterium tuberculosis infection 185 Vietnamese ancestry uninfected cases, 353 Vietnamese ancestry infected controls 30 uninfected cases, 127 infected controls, 118 South African Coloured uninfected cases, 136 South African Coloured uninfected controls Illumina [5591951] (imputed) 1 decreased susceptibility to bacterial infection http://www.ebi.ac.uk/efo/EFO_0008322 GCST011663 Genome-wide genotyping array 2021-05-14 33661925 Quistrebert J 2021-03-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33661925 Genome-wide association study of resistance to Mycobacterium tuberculosis infection identifies a locus at 10q26.2 in three distinct populations. Resistance to Mycobacterium tuberculosis infection 185 Vietnamese ancestry uninfected cases, 201 Vietnamese ancestry infected controls NA Illumina [5591951] (imputed) 1 decreased susceptibility to bacterial infection http://www.ebi.ac.uk/efo/EFO_0008322 GCST011664 Genome-wide genotyping array 2020-07-21 32271837 Im SW 2020-04-09 PLoS One www.ncbi.nlm.nih.gov/pubmed/32271837 A population-specific low-frequency variant of SLC22A12 (p.W258*) explains nearby genome-wide association signals for serum uric acid concentrations among Koreans. Serum uric acid levels 1,902 Korean ancestry males 2,912 Korean ancestry individuals Illumina [4414664] (imputed) 2 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST010283 Genome-wide genotyping array 2021-08-20 33667223 Lesseur C 2021-03-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33667223 Genome-wide association meta-analysis identifies pleiotropic risk loci for aerodigestive squamous cell cancers. Aerodigestive squamous cell cancer (pleiotropy) 7,426 European ancestry lung squamous cell carcinoma cases, 5,452 European ancestry oral and oropharynx squamous cell carcinoma cases, 693 European ancestry laryngeal squamous cell carcinoma cases, 316 European ancestry esophageal squamous cell carcinoma cases, 61,961 European ancestry controls NA Illumina [8468885] (imputed) 175 upper aerodigestive tract neoplasm http://www.ebi.ac.uk/efo/EFO_0004284 GCST012213 Genome-wide genotyping array 2019-01-28 30535121 Gao XR 2018-12-07 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30535121 Genome-wide association analyses identify 139 loci associated with macular thickness in the UK Biobank cohort. Macular thickness 59,814 European ancestry individuals 8,609 European ancestry individuals Affymetrix [11100000] (imputed) 139 macula measurement http://www.ebi.ac.uk/efo/EFO_0008375 GCST006976 Genome-wide genotyping array 2019-06-03 31065058 Rongve A 2019-05-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31065058 GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study. Dementia with Lewy bodies 720 European ancestry cases, 6,490 European ancestry controls 108 European ancestry cases, 75,545 European ancestry controls Illumina [6963063] (imputed) 2 Lewy body dementia http://www.ebi.ac.uk/efo/EFO_0006792 GCST007881 Genome-wide genotyping array 2022-05-27 35235886 Song W 2022-02-17 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/35235886 Genome-wide identification of the shared genetic basis of cannabis and cigarette smoking and schizophrenia implicates NCAM1 and neuronal abnormality. Cannabis smoking or cigarette smoking or schizophrenia 780,649 European ancestry individuals NA NR [NR] 20 smoking status measurement, Cannabis use, schizophrenia http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0007585, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90103805 Genome-wide genotyping array 2020-03-23 31900429 Sliz E 2020-01-03 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31900429 A variant near DHCR24 associates with microstructural properties of white matter and peripheral lipid metabolism in adolescents. Visceral fat, circulating phospholipid PC(16:0/2:0) and white matter microstructure (shared variance) 872 French-Canadian (founder/genetic isolate) ancestry adolescents from up to 486 families NA Illumina [8511049] (imputed) 1 visceral adipose tissue measurement, white matter microstructure measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004765, http://www.ebi.ac.uk/efo/EFO_0005674, http://www.ebi.ac.uk/efo/EFO_0004639 GCST009780 Genome-wide genotyping array 2021-08-13 33574088 Mocci E 2021-02-11 Cancer Res www.ncbi.nlm.nih.gov/pubmed/33574088 Smoking modifies pancreatic cancer risk loci on 2q21.3. Pancreatic ductal adenocarcinoma x smoking interaction 7,937 European ancestry cases, 11,774 European ancestry controls NA Illumina [6769447] (imputed) 4 smoking status measurement, pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0002618 GCST012178 Genome-wide genotyping array 2021-02-08 33536424 Wang YF 2021-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33536424 Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups. Systemic lupus erythematosus 4,222 Han Chinese ancestry cases, 8,431 Han Chinese ancestry controls NA Illumina [5719137] (imputed) 22 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90011866 Genome-wide genotyping array 2021-02-08 33536424 Wang YF 2021-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33536424 Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups. Systemic lupus erythematosus 4,576 European ancestry cases, 8,039 European ancestry controls NA NR [NR] (imputed) 8 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST011097 Genome-wide genotyping array 2021-02-08 33536424 Wang YF 2021-02-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33536424 Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups. Systemic lupus erythematosus 4,222 Han Chinese ancestry cases, 8,431 Han Chinese ancestry controls, 4,576 European ancestry cases, 8,039 European ancestry controls NA Illumina [NR] (imputed) 35 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST011096 Genome-wide genotyping array 2021-07-27 33685280 Nishizawa D 2021-01-01 Mol Pain www.ncbi.nlm.nih.gov/pubmed/33685280 Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Chronic pain 191 Japanese ancestry cases, 282 Japanese ancestry controls NA Illumina [445723] 6 Chronic pain http://purl.obolibrary.org/obo/HP_0012532 GCST012125 Genome-wide genotyping array 2021-07-27 33685280 Nishizawa D 2021-01-01 Mol Pain www.ncbi.nlm.nih.gov/pubmed/33685280 Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Postherpetic neuralgia 89 Japanese ancestry cases, 282 Japanese ancestry controls NA Illumina [445723] 5 postherpetic neuralgia http://purl.obolibrary.org/obo/MONDO_0041052 GCST012124 Genome-wide genotyping array 2021-07-27 33685280 Nishizawa D 2021-01-01 Mol Pain www.ncbi.nlm.nih.gov/pubmed/33685280 Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Response to opiods (pain relief efficacy) 50 Japanese ancestry individuals NA Illumina [445723] 1 pain measurement, response to opioid http://www.ebi.ac.uk/efo/EFO_0010639, http://www.ebi.ac.uk/efo/EFO_0008541 GCST012123 Genome-wide genotyping array 2021-07-27 33685280 Nishizawa D 2021-01-01 Mol Pain www.ncbi.nlm.nih.gov/pubmed/33685280 Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Response to antidepressants (pain relief efficacy) 66 Japanese ancestry individuals NA Illumina [445723] 1 pain measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0010639, http://purl.obolibrary.org/obo/GO_0036276 GCST012122 Genome-wide genotyping array 2021-07-27 33685280 Nishizawa D 2021-01-01 Mol Pain www.ncbi.nlm.nih.gov/pubmed/33685280 Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Response to anticonvulsants (pain relief efficacy) 99 Japanese ancestry individuals NA Illumina [445723] 1 pain measurement, response to anticonvulsant http://www.ebi.ac.uk/efo/EFO_0010639, http://purl.obolibrary.org/obo/GO_0036277 GCST012121 Genome-wide genotyping array 2021-07-27 33685280 Nishizawa D 2021-01-01 Mol Pain www.ncbi.nlm.nih.gov/pubmed/33685280 Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Response to non-steroidal anti-inflammatory drugs (pain relief efficacy) 25 Japanese ancestry individuals NA Illumina [445723] 2 pain measurement, response to non-steroidal anti-inflammatory http://www.ebi.ac.uk/efo/EFO_0010639, http://www.ebi.ac.uk/efo/EFO_0005533 GCST012120 Genome-wide genotyping array 2021-07-27 33685280 Nishizawa D 2021-01-01 Mol Pain www.ncbi.nlm.nih.gov/pubmed/33685280 Genome-wide association study identifies candidate loci associated with chronic pain and postherpetic neuralgia. Response to gamma-aminobutyric acid receptor agonists (pain relief efficacy) 58 Japanese ancestry individuals NA Illumina [445723] 1 pain measurement, response to gamma-aminobutyric acid receptor agonists http://www.ebi.ac.uk/efo/EFO_0010639, http://www.ebi.ac.uk/efo/EFO_0600022 GCST012119 Genome-wide genotyping array 2021-04-12 33485957 Patrick MT 2021-01-21 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/33485957 Associations between COVID-19 and skin conditions identified through epidemiology and genomic studies. COVID-19 or psoriasis (trans-disease meta-analysis) 1,678 COVID-19 cases, 11,024 psoriasis cases, 690,971 controls NA NR [NR] 1 psoriasis, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000676, http://purl.obolibrary.org/obo/MONDO_0100096 GCST011477 Genome-wide genotyping array 2021-04-12 33485957 Patrick MT 2021-01-21 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/33485957 Associations between COVID-19 and skin conditions identified through epidemiology and genomic studies. COVID-19 or atopic dermatitis (trans-disease meta-analysis) 30,937 COVID-19 cases, 21,000 atopic dermatitis cases, 1,566,815 controls NA NR [NR] 1 atopic eczema, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000274, http://purl.obolibrary.org/obo/MONDO_0100096 GCST011476 Genome-wide genotyping array 2021-08-23 33704824 Vandebergh M 2021-03-11 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/33704824 Genetic variation in WNT9B increases relapse hazard in multiple sclerosis. Relapse in treatment-naive multiple sclerosis (time to event) 506 European or unknown ancestry individuals 485 individuals Illumina [7344935] (imputed) 1 disease recurrence, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0004952, http://purl.obolibrary.org/obo/MONDO_0005301 GCST012218 Genome-wide genotyping array 2021-07-27 33495597 Harper AR 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495597 Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. Hypertrophic cardiomyopathy 233 African ancestry cases, 122 Hispanic/Latino cases, 70 East Asian ancestry cases, 2,196 European ancestry cases, 138 South Asian ancestry cases, 21 cases, 1,331 African ancestry controls, 170 Hispanic/Latino controls, 333 East Asian ancestry controls, 42,902 European ancestry controls, 1,727 South Asian ancestry controls, 1,023 controls 1,643 European or unknown ancestry cases, 6,628 European or unknown ancestry controls Affymetrix [8590397] (imputed) 12 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST012101 Genome-wide genotyping array, Genome-wide sequencing 2021-07-27 33495597 Harper AR 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495597 Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. Hypertrophic cardiomyopathy (sarcomere positive) 54 African ancestry cases, 28 Hispanic/Latino cases, 18 East Asian ancestry cases, 728 European ancestry cases, 43 South Asian ancestry cases, 593 African ancestry controls, 92 Hispanic/Latino controls, 121 East Asian ancestry controls, 18,791 European ancestry controls, 595 South Asian ancestry controls NA Affymetrix [8590397] (imputed) 20 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST012100 Genome-wide genotyping array 2021-07-27 33495597 Harper AR 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495597 Common genetic variants and modifiable risk factors underpin hypertrophic cardiomyopathy susceptibility and expressivity. Hypertrophic cardiomyopathy (sarcomere negative) 170 African ancestry cases, 93 Hispanic/Latino cases, 52 East Asian ancestry cases, 1,444 European ancestry cases, 94 South Asian ancestry cases, 21 cases, 738 African ancestry controls, 78 Hispanic/Latino controls, 212 East Asian ancestry controls, 24,161 European ancestry controls, 1,132 South Asian ancestry controls, 1,023 controls NA Affymetrix [8590397] (imputed) 25 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST012099 Genome-wide genotyping array, Genome-wide sequencing 2021-08-13 33560138 Dube MP 2021-02-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33560138 Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT. Cardiovascular event in colchicine-treated recent myocardial infarction (time to event) 39 European ancestry cases, 663 European ancestry controls NA Illumina [4462492] (imputed) 1 cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0006919 GCST012188 Genome-wide genotyping array 2021-08-13 33560138 Dube MP 2021-02-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33560138 Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT. Cardiovascular event in colchicine-treated recent myocardial infarction (time to event) 30 European ancestry male cases, 546 European ancestry male controls NA Illumina [4455743] (imputed) 1 cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0006919 GCST012187 Genome-wide genotyping array 2021-08-13 33560138 Dube MP 2021-02-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33560138 Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT. Gastrointestinal event in colchicine-treated recent myocardial infarction (time to event) 187 European ancestry cases, 580 European ancestry controls NA Illumina [4468817] (imputed) 2 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST012186 Genome-wide genotyping array 2021-08-13 33560138 Dube MP 2021-02-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/33560138 Pharmacogenomics of the Efficacy and Safety of Colchicine in COLCOT. Gastrointestinal event in colchicine-treated recent myocardial infarction (time to event) 622 European ancestry men NA Illumina [4468817] (imputed) 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST012185 Genome-wide genotyping array 2021-08-20 33693791 Park S 2021-03-09 J Nutr www.ncbi.nlm.nih.gov/pubmed/33693791 Observational or Genetically Predicted Higher Vegetable Intake and Kidney Function Impairment: An Integrated Population-Scale Cross-Sectional Analysis and Mendelian Randomization Study. Vegetable consumption 337,128 European ancestry individuals NA NR [NR] (imputed) 8 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST012216 Genome-wide genotyping array 2021-03-22 33491310 Warner ET 2021-02-01 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/33491310 A Genome-Wide Association Study of Childhood Body Fatness. Childhood body fatness 34,401 European ancestry individuals NA Affymetrix, Illumina [10031233] (imputed) 14 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST011370 Genome-wide genotyping array 2021-02-11 33357513 Chen HH 2020-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33357513 Host genetic effects in pneumonia. Pneumonia severity 5,774 European ancestry inpatients, 1,043 African ancestry inpatients, 3,115 European ancestry outpatients, 667 African ancestry outpatients 850 European ancestry inpatients, 220 African ancestry inpatients, 274 European ancestry outpatients, 72 African ancestry outpatients Illumina [up to 7594451] (imputed) 0 pneumonia severity measurement http://www.ebi.ac.uk/efo/EFO_0010966 GCST011103 Genome-wide genotyping array 2021-02-11 33357513 Chen HH 2020-12-13 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33357513 Host genetic effects in pneumonia. Pneumonia 8,889 European ancestry cases, 1,710 African ancestry cases, 60,767 European ancestry controls, 13,871 African ancestry controls 8,805 European ancestry cases, 368 African ancestry cases, 447,334 European ancestry controls, 10,417 African ancestry controls Illumina [up to 13633982] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST011104 Genome-wide genotyping array 2021-04-21 33729212 Suri P 2021-02-04 Pain www.ncbi.nlm.nih.gov/pubmed/33729212 Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis. Lumbar spinal stenosis 8,326 European ancestry cases, 97,106 European ancestry controls 3,239 European ancestry cases, 268,755 European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST011523 Genome-wide genotyping array 2021-04-21 33729212 Suri P 2021-02-04 Pain www.ncbi.nlm.nih.gov/pubmed/33729212 Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis. Lumbosacral radicular syndrome or lumbar spinal stenosis 23,411 European ancestry cases, 82,405 European ancestry controls 18,169 European ancestry cases, 267,742 European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 spinal stenosis, Sciatica http://www.ebi.ac.uk/efo/EFO_0007490, http://purl.obolibrary.org/obo/HP_0011868 GCST011522 Genome-wide genotyping array 2021-04-21 33729212 Suri P 2021-02-04 Pain www.ncbi.nlm.nih.gov/pubmed/33729212 Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis. Lumbosacral radicular syndrome 20,838 European ancestry cases, 84,642 European ancestry controls 16,575 European ancestry cases, 267,860 European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST011524 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Corticospinal tract R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003883 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Corticospinal tract L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003884 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Medial lemniscus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003885 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Medial lemniscus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003886 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Inferior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003887 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Inferior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003888 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003889 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003890 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Cerebral peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003891 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Cerebral peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003892 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Anterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003893 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Anterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003894 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Posterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003895 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Posterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003896 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Retrolenticular part of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003897 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Retrolenticular part of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003898 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Anterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003899 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Anterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003900 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003901 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003902 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Posterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003903 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Posterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003904 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Posterior thalamic radiation R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003905 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Posterior thalamic radiation L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003906 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Sagittal stratum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003907 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Sagittal stratum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003908 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA External capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003909 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA External capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003910 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Cingulum cingulate gyrus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003911 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Cingulum cingulate gyrus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003912 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Cingulum hippocampus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003913 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Cingulum hippocampus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003914 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Fornix cres+Stria terminalis R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003915 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Fornix cres+Stria terminalis L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003916 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior longitudinal fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003917 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior longitudinal fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003918 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior fronto-occipital fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003919 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Superior fronto-occipital fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003920 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Uncinate fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003921 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Uncinate fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003922 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Tapetum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003923 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Tapetum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003924 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ar l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003925 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ar r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003926 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA atr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003927 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA atr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003928 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA cgc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003929 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA cgc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003930 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA cgh l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003931 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA cgh r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003932 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA cst l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003933 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA cst r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003934 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA fma 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003935 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA fmi 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 6 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003936 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ifo l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003937 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ifo r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003938 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ilf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003939 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ilf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003940 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA mcp 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003941 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ml l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003942 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ml r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003943 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ptr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003944 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA ptr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003945 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA slf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003946 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA slf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003947 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA str l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003948 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA str r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003949 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA unc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003950 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX FA unc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003951 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Middle cerebellar peduncle 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003952 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 424) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005277 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 425) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005278 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 426) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005279 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 427) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005280 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 428) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005281 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 429) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005282 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 430) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005283 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002806 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002807 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002808 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002809 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002810 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002811 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002812 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002813 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002814 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002815 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002816 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002817 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002818 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002819 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002820 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002821 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002822 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002823 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002824 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002825 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002826 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002827 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002828 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002829 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002830 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002831 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume frontalpole 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002832 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002833 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002834 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002835 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002836 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA3a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002837 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA3b 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002838 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA4a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002839 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA4p 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002840 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA6 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002841 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA44 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002842 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume BA45 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002843 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume V1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002844 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume V2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002845 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume MT 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002846 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume perirhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002847 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh volume entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002848 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Corticospinal tract R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003958 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Corticospinal tract L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003959 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Medial lemniscus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003960 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Medial lemniscus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003961 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Inferior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003962 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Inferior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003963 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003964 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 381) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005234 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 382) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005235 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 383) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005236 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 384) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005237 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 385) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005238 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 386) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005239 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 387) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005240 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 388) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005241 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 389) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005242 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 390) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005243 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 391) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005244 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 392) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005245 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 393) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005246 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 394) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005247 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 395) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005248 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 396) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005249 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 397) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005250 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 398) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005251 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 399) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005252 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 400) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005253 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 401) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005254 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 402) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005255 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 403) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005256 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 404) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005257 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 405) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005258 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 406) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005259 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 407) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005260 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 408) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005261 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 409) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005262 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 410) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005263 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 411) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005264 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 412) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005265 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 413) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005266 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 414) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005267 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 415) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005268 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 416) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005269 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 417) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005270 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 418) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005271 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 419) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005272 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 420) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005273 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 421) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005274 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 422) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005275 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 423) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005276 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Pontine crossing tract 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003953 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Genu of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003954 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Body of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003955 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Splenium of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003956 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Fornix 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003957 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003083 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area lateralorbitofrontal 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003084 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003085 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003086 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003087 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003088 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003089 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003090 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003091 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003092 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003093 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003094 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003095 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003096 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003097 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Cingulum cingulate gyrus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004157 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Cingulum cingulate gyrus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004158 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Cingulum hippocampus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004159 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Cingulum hippocampus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004160 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Fornix cres+Stria terminalis R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004161 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Fornix cres+Stria terminalis L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004162 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior longitudinal fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004163 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior longitudinal fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004164 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior fronto-occipital fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004165 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior fronto-occipital fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004166 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Uncinate fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004167 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Uncinate fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004168 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Tapetum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004169 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Tapetum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004170 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Middle cerebellar peduncle 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004171 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Pontine crossing tract 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004172 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Genu of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004173 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Body of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004174 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Splenium of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004175 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Fornix 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004176 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Corticospinal tract R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004177 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Corticospinal tract L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004178 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Medial lemniscus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004179 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Medial lemniscus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004180 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Inferior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004181 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Inferior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004182 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004183 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004184 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Cerebral peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004185 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Cerebral peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004186 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Anterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004187 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Anterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004188 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Posterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004189 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Posterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004190 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Retrolenticular part of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004191 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Retrolenticular part of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004192 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Anterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004193 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Anterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004194 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004195 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004196 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Posterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004197 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Posterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004198 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Posterior thalamic radiation R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004199 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Posterior thalamic radiation L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004200 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Sagittal stratum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 6 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004201 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Sagittal stratum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004202 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 External capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004203 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 External capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004204 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Cingulum cingulate gyrus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004205 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Cingulum cingulate gyrus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004206 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Cingulum hippocampus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004207 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Cingulum hippocampus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004208 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Fornix cres+Stria terminalis R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004209 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Fornix cres+Stria terminalis L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004210 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior longitudinal fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004211 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior longitudinal fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004212 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior fronto-occipital fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004213 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Superior fronto-occipital fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004214 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Uncinate fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004215 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Uncinate fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004216 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-oc-temp-lat 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003058 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-oc-temp-med+Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003059 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-orbital-lateral 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003060 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-orbital-med-olfact 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003061 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-orbital-H-Shaped 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003062 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-parieto-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003063 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-pericallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003064 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003065 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-precentral-inf-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003066 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-precentral-sup-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003067 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-suborbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003068 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-subparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003069 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003070 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-temporal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003071 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-temporal-transverse 21,280 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003072 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area TotalSurface 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003073 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003074 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003075 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003076 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003077 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003078 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003079 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003080 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003081 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area isthmuscingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003082 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-temp-sup-Plan-polar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003033 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-temp-sup-Plan-tempo 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003034 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003035 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-temporal-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003036 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume Lat-Fis-ant-Horizont 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003037 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume Lat-Fis-ant-Vertical 21,269 British ancestry individuals 10,683 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003038 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume Lat-Fis-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003039 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume Pole-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003040 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume Pole-temporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003041 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-calcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003042 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003043 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-cingul-Marginalis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003044 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-circular-insula-ant 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003045 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-circular-insula-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003046 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-circular-insula-sup 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003047 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-collat-transv-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003048 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-collat-transv-post 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003049 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-front-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003050 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003051 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003052 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-interm-prim-Jensen 21,279 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003053 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-intrapariet+P-trans 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003054 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-oc-middle+Lunatus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003055 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-oc-sup+transversal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003056 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume S-occipital-ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003057 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-1-receptor antagonist levels 532 Sub-Saharan African ancestry men 391 African American men Affymetrix, Illumina [NR] (imputed) 1 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90091149 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-1-receptor antagonist levels in overweight individuals 1,339 Sub-Saharan African ancestry individuals 883 African American individuals Affymetrix, Illumina [NR] (imputed) 0 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90204152 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-1-receptor antagonist levels in type 2 diabetes 559 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90204153 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-1-receptor antagonist levels 807 Sub-Saharan African ancestry women 492 African American women Affymetrix, Illumina [NR] (imputed) 0 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90204150 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Insulin levels 2,061 Sub-Saharan African ancestry individuals, 7,645 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90091146 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Insulin levels in lean individuals 974 Sub-Saharan African ancestry individuals 1,563 African American individuals Affymetrix, Illumina [NR] (imputed) 17 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90091171 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Insulin levels 2,061 Sub-Saharan African ancestry men 2,596 African American men Affymetrix, Illumina [NR] (imputed) 12 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90091152 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Insulin levels in overweight individuals 1,087 Sub-Saharan African ancestry individuals 4,874 African American individuals Affymetrix, Illumina [NR] (imputed) 11 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90091182 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Insulin levels 2,061 Sub-Saharan African ancestry individuals 6,437 African American individuals Affymetrix, Illumina [NR] (imputed) 13 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90091194 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Insulin levels 2,061 Sub-Saharan African ancestry women 3,841 African American women Affymetrix, Illumina [NR] (imputed) 10 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90091161 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Leptin levels 3,745 Sub-Saharan African ancestry individuals, 1,869 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 2 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90091135 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Leptin levels in lean individuals 1,582 Sub-Saharan African ancestry individuals 606 African American individuals Affymetrix, Illumina [NR] (imputed) 5 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90091167 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Leptin levels 1,550 Sub-Saharan African ancestry men 737 African American men Affymetrix, Illumina [NR] (imputed) 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90204147 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Leptin levels in overweight individuals 2,163 Sub-Saharan African ancestry individuals 1,263 African American individuals Affymetrix, Illumina [NR] (imputed) 3 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90091177 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Leptin levels in type 2 diabetes 1,850 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90091200 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Leptin levels 1,895 Sub-Saharan African ancestry individuals 1,869 African American individuals Affymetrix, Illumina [NR] (imputed) 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90204148 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Leptin levels 2,195 Sub-Saharan African ancestry women 1,132 African American women Affymetrix, Illumina [NR] (imputed) 1 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90091158 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Plasminogen activator inhibitor type 1 levels (PAI-1) 3,807 Sub-Saharan African ancestry individuals, 594 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 2 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90091137 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Plasminogen activator inhibitor type 1 levels (PAI-1) in lean individuals 1,572 Sub-Saharan African ancestry individuals 594 African American individuals Affymetrix, Illumina [NR] (imputed) 2 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90091170 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Plasminogen activator inhibitor type 1 levels (PAI-1) 1,544 Sub-Saharan African ancestry men 259 African American men Affymetrix, Illumina [NR] (imputed) 0 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90204149 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Plasminogen activator inhibitor type 1 levels (PAI-1) in overweight individuals 2,235 Sub-Saharan African ancestry individuals 594 African American individuals Affymetrix, Illumina [NR] (imputed) 3 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90091180 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Plasminogen activator inhibitor type 1 levels (PAI-1) in type 2 diabetes 1,871 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 3 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90091202 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Plasminogen activator inhibitor type 1 levels (PAI-1) 1,936 Sub-Saharan African ancestry individuals 469 African American individuals Affymetrix, Illumina [NR] (imputed) 2 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90091190 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Plasminogen activator inhibitor type 1 levels (PAI-1) 2,263 Sub-Saharan African ancestry women 335 African American women Affymetrix, Illumina [NR] (imputed) 5 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90091160 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Resistin levels 3,754 Sub-Saharan African ancestry individuals, 1,867 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90091142 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Resistin levels in lean individuals 1,560 Sub-Saharan African ancestry individuals 603 African American individuals Affymetrix, Illumina [NR] (imputed) 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90091174 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Resistin levels 1,523 Sub-Saharan African ancestry men 733 African American men Affymetrix, Illumina [NR] (imputed) 2 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90091155 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Resistin levels in overweight individuals 2,194 Sub-Saharan African ancestry individuals 1,264 African American individuals Affymetrix, Illumina [NR] (imputed) 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90091185 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Resistin levels in type 2 diabetes 1,831 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90091204 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Resistin levels 1,923 Sub-Saharan African ancestry individuals 1,658 African American individuals Affymetrix, Illumina [NR] (imputed) 2 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90091197 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Resistin levels 2,231 Sub-Saharan African ancestry women 1,134 African American women Affymetrix, Illumina [NR] (imputed) 2 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90091164 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Visfatin levels 3,742 Sub-Saharan African ancestry individuals, 1,857 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 1 visfatin measurement http://www.ebi.ac.uk/efo/EFO_0801230 GCST90091143 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Visfatin levels in lean individuals 1,403 Sub-Saharan African ancestry individuals 1,857 African American individuals Affymetrix, Illumina [NR] (imputed) 1 visfatin measurement http://www.ebi.ac.uk/efo/EFO_0801230 GCST90091175 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Visfatin levels 1,515 Sub-Saharan African ancestry men 719 African American men Affymetrix, Illumina [NR] (imputed) 1 visfatin measurement http://www.ebi.ac.uk/efo/EFO_0801230 GCST90091156 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Visfatin levels in overweight individuals 2,202 Sub-Saharan African ancestry individuals 1,857 African American individuals Affymetrix, Illumina [NR] (imputed) 1 visfatin measurement http://www.ebi.ac.uk/efo/EFO_0801230 GCST90091186 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Visfatin levels in type 2 diabetes 1,844 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 7 visfatin measurement http://www.ebi.ac.uk/efo/EFO_0801230 GCST90091205 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Visfatin levels 1,898 Sub-Saharan African ancestry individuals 1,633 African American individuals Affymetrix, Illumina [NR] (imputed) 1 visfatin measurement http://www.ebi.ac.uk/efo/EFO_0801230 GCST90091198 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Visfatin levels 2,227 Sub-Saharan African ancestry women 1,123 African American women Affymetrix, Illumina [NR] (imputed) 2 visfatin measurement http://www.ebi.ac.uk/efo/EFO_0801230 GCST90091165 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. ghrelin levels in type 2 diabetes 1,860 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST90091203 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. ghrelin levels 1,917 Sub-Saharan African ancestry individuals 1,649 African American individuals Affymetrix, Illumina [NR] (imputed) 2 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST90091196 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. ghrelin levels 2,241 Sub-Saharan African ancestry women 1,129 African American women Affymetrix, Illumina [NR] (imputed) 5 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST90091163 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucose-dependent insulinotropic peptide levels 3,751 Sub-Saharan African ancestry individuals, 1,866 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 1 glucose-dependent insulinotropic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008464 GCST90091136 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucose-dependent insulinotropic peptide levels in lean individuals 1,548 Sub-Saharan African ancestry individuals 610 African American individuals Affymetrix, Illumina [NR] (imputed) 2 glucose-dependent insulinotropic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008464 GCST90091168 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucose-dependent insulinotropic peptide levels 1,522 Sub-Saharan African ancestry men 739 African American men Affymetrix, Illumina [NR] (imputed) 0 glucose-dependent insulinotropic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008464 GCST90204164 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucose-dependent insulinotropic peptide levels in overweight individuals 2,203 Sub-Saharan African ancestry individuals 1,256 African American individuals Affymetrix, Illumina [NR] (imputed) 11 glucose-dependent insulinotropic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008464 GCST90091178 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucose-dependent insulinotropic peptide levels in type 2 diabetes 1,844 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 glucose-dependent insulinotropic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008464 GCST90091201 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucose-dependent insulinotropic peptide levels 1,907 Sub-Saharan African ancestry individuals 1,653 African American individuals Affymetrix, Illumina [NR] (imputed) 15 glucose-dependent insulinotropic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008464 GCST90091188 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucose-dependent insulinotropic peptide levels 2,229 Sub-Saharan African ancestry women 1,127 African American women Affymetrix, Illumina [NR] (imputed) 9 glucose-dependent insulinotropic peptide measurement http://www.ebi.ac.uk/efo/EFO_0008464 GCST90091159 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon-like peptide-1 levels 3,783 Sub-Saharan African ancestry individuals, 1,806 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 0 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90091144 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon-like peptide-1 levels in lean individuals 1,565 Sub-Saharan African ancestry individuals 568 African American individuals Affymetrix, Illumina [NR] (imputed) 2 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90091169 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003266 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003267 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003268 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003269 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003270 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003271 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003272 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Anterior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004349 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Anterior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004350 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004351 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004352 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Posterior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004353 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Posterior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004354 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Posterior thalamic radiation R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 11 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004355 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Posterior thalamic radiation L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004356 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Sagittal stratum R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004357 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Sagittal stratum L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 12 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004358 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF External capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004359 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF External capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004360 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Cingulum cingulate gyrus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004361 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Cingulum cingulate gyrus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004362 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Cingulum hippocampus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004363 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Cingulum hippocampus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004364 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Fornix cres+Stria terminalis R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004365 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Fornix cres+Stria terminalis L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004366 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon-like peptide-1 levels 1,534 Sub-Saharan African ancestry men 1,199 African American men Affymetrix, Illumina [NR] (imputed) 2 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90091148 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon-like peptide-1 levels in overweight individuals 2,218 Sub-Saharan African ancestry individuals 1,230 African American individuals Affymetrix, Illumina [NR] (imputed) 3 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90091179 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon-like peptide-1 levels in type 2 diabetes 1,860 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90204159 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon-like peptide-1 levels 1,923 Sub-Saharan African ancestry individuals 1,806 African American individuals Affymetrix, Illumina [NR] (imputed) 1 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90091189 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Adipsin levels 3,713 Sub-Saharan African ancestry individuals, 1,846 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 2 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90091134 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Adipsin levels in lean individuals 1,547 Sub-Saharan African ancestry individuals 605 African American individuals Affymetrix, Illumina [NR] (imputed) 5 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90091166 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Adipsin levels 1,510 Sub-Saharan African ancestry men 724 African American men Affymetrix, Illumina [NR] (imputed) 24 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90091147 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Adipsin levels in overweight individuals 2,166 Sub-Saharan African ancestry individuals 1,241 African American individuals Affymetrix, Illumina [NR] (imputed) 9 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90091176 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Adipsin levels in type 2 diabetes 1,820 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 19 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90091199 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Adipsin levels 1,893 Sub-Saharan African ancestry individuals 1,643 African American individuals Affymetrix, Illumina [NR] (imputed) 6 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90091187 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Adipsin levels 2,203 Sub-Saharan African ancestry women 1,122 African American women Affymetrix, Illumina [NR] (imputed) 5 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90091157 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. ghrelin levels 3,777 Sub-Saharan African ancestry individuals, 1,858 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 2 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST90091141 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. ghrelin levels in lean individuals 1,557 Sub-Saharan African ancestry individuals 597 African American individuals Affymetrix, Illumina [NR] (imputed) 3 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST90091173 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. ghrelin levels 1,536 Sub-Saharan African ancestry men 729 African American men Affymetrix, Illumina [NR] (imputed) 3 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST90091154 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. ghrelin levels in overweight individuals 2,220 Sub-Saharan African ancestry individuals 1,261 African American individuals Affymetrix, Illumina [NR] (imputed) 4 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST90091184 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003241 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003242 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003243 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003244 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003245 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003246 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003247 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003248 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003249 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003250 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003251 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003252 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003253 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003254 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003255 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003256 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003257 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area rostralanteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003258 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003259 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003260 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003261 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003262 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003263 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003264 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003265 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Coriobacteriaceae id.811) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016933 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Defluviitaleaceae id.1924) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016934 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Desulfovibrionaceae id.3169) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016935 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Enterobacteriaceae id.3469) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016936 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Erysipelotrichaceae id.2149) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016937 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Family XI id.1936) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016938 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Family XIII id.1957) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016939 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Lachnospiraceae id.1987) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016940 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Lactobacillaceae id.1836) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016941 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Methanobacteriaceae id.121) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016942 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Oxalobacteraceae id.2966) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016943 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Pasteurellaceae id.3689) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016944 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Peptococcaceae id.2024) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016945 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Peptostreptococcaceae id.2042) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016946 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Porphyromonadaceae id.943) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016947 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Prevotellaceae id.960) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016948 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Rhodospirillaceae id.2717) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016949 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Rikenellaceae id.967) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016950 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Ruminococcaceae id.2050) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016951 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Streptococcaceae id.1850) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 5 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016952 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG010 id.11367) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017058 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG011 id.11368) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017059 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG013 id.11370) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017060 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG014 id.11371) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017061 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcus1 id.11373) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017062 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Veillonella id.2198) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017088 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Victivallis id.2256) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017089 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Actinomycetales id.420) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017090 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Bacillales id.1674) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017091 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Bacteroidales id.913) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017092 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Bifidobacteriales id.432) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017093 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Burkholderiales id.2874) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017094 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Clostridiales id.1863) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017095 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Coriobacteriales id.810) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017096 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Desulfovibrionales id.3156) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017097 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Enterobacteriales id.3468) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017098 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Erysipelotrichales id.2148) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017099 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Gastranaerophilales id.1591) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017100 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown family id.1000001214) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016953 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown family id.1000005471) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016954 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown family id.1000006161) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016955 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Veillonellaceae id.2172) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016956 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Verrucomicrobiaceae id.4036) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016957 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Victivallaceae id.2255) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016958 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Actinomyces id.423) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016959 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Adlercreutzia id.812) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016960 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Akkermansia id.4037) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016961 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Alistipes id.968) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016962 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Allisonella id.2174) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016963 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Lactobacillales id.1800) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017101 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Methanobrevibacter id.123) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017033 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Odoribacter id.952) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017034 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Olsenella id.822) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017035 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Oscillibacter id.2063) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017036 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Oscillospira id.2064) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017037 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Oxalobacter id.2978) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017038 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Parabacteroides id.954) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017039 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Paraprevotella id.962) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017040 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Parasutterella id.2892) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017041 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Peptococcus id.2037) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 6 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017042 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Phascolarctobacterium id.2168) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017043 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Prevotella7 id.11182) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017044 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Prevotella9 id.11183) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017045 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Rikenellaceae RC9 gut group id.11191) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017046 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Romboutsia id.11347) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017047 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Roseburia id.2012) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017048 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminiclostridium5 id.11355) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017049 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminiclostridium6 id.11356) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017050 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminiclostridium9 id.11357) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017051 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae NK4A214 group id.11358) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017052 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG002 id.11360) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017053 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG003 id.11361) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017054 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG004 id.11362) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017055 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG005 id.11363) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017056 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcaceae UCG009 id.11366) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017057 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcus2 id.11374) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017063 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcus gauvreauii group id.11342) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017064 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcus gnavus group id.14376) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017065 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Ruminococcus torques group id.14377) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017066 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Sellimonas id.14369) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017067 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Senegalimassilia id.11160) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017068 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Slackia id.825) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017069 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Streptococcus id.1853) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017070 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Subdoligranulum id.2070) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017071 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Sutterella id.2896) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017072 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Terrisporobacter id.11348) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017073 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Turicibacter id.2162) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017074 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Tyzzerella3 id.11335) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017075 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.1000000073) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017076 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.1000001215) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017077 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.1000005472) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017078 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.1000005479) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017079 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.1000006162) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017080 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.1868) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017081 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.2001) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017082 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.2041) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017083 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.2071) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017084 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.2755) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017085 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.826) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017086 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (unknown genus id.959) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017087 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Family XIII AD3011 group id.11293) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017008 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Family XIII UCG001 id.11294) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017009 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Flavonifractor id.2059) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017010 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Fusicatenibacter id.11305) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017011 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Gordonibacter id.821) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017012 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Haemophilus id.3698) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017013 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Holdemanella id.11393) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017014 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Holdemania id.2157) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017015 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Howardella id.2000) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017016 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Hungatella id.11306) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017017 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Intestinibacter id.11345) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017018 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Intestinimonas id.2062) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017019 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnoclostridium id.11308) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017020 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae FCS020 group id.11314) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017021 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae NC2004 group id.11316) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017022 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae ND3007 group id.11317) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017023 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae NK4A136 group id.11319) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017024 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae UCG001 id.11321) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017025 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae UCG004 id.11324) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017026 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae UCG008 id.11328) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017027 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospiraceae UCG010 id.11330) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017028 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lachnospira id.2004) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017029 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lactobacillus id.1837) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017030 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Lactococcus id.1851) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017031 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Marvinbryantia id.2005) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017032 Genome-wide genotyping array 2019-04-09 30529582 Lu Y 2018-12-06 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/30529582 Large-scale Genome-wide Association Study of East Asians Identifies Loci Associated With Risk for Colorectal Cancer. Colorectal cancer 22,775 East Asian ancestry cases, 47,731 East Asian ancestry controls NA Affymetrix, Illumina [up to 10700000] (imputed) 40 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST007552 Genome-wide genotyping array, Exome genotyping array 2021-08-26 33706416 Slob EMA 2021-03-11 Pediatr Allergy Immunol www.ncbi.nlm.nih.gov/pubmed/33706416 Genome-wide association studies of exacerbations in children using long-acting beta2-agonists. Childhood asthma exacerbations in long-acting beta2-agonist treatment 642 European, Hispanic, African, Asian or unknown ancestry cases, 783 European, Hispanic, African, Asian or unknown ancestry controls NA Affymetrix, Illumina [82996] (imputed) 8 asthma exacerbation measurement http://www.ebi.ac.uk/efo/EFO_0007614 GCST012244 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and HDL-C (pairwise) 277,811 European ancestry individuals, 10,022 East Asian, South Asian and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 17 body fat percentage, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007800, http://www.ebi.ac.uk/efo/EFO_0004612 GCST011344 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and LDL-C (pairwise) 263,726 European ancestry individuals, 10,061 East Asian, South Asian and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 8 low density lipoprotein cholesterol measurement, body fat percentage http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007800 GCST011343 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and triglycerides (pairwise) 268,505 European ancestry individuals, 10,072 East Asian, South Asian and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 15 triglyceride measurement, body fat percentage http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0007800 GCST011342 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and fasting insulin (pairwise) 142,394 European ancestry individuals, 10,072 East Asian, South Asian and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 4 body fat percentage, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0007800, http://www.ebi.ac.uk/efo/EFO_0004466 GCST011341 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and fasting glucose (pairwise) 148,718 European ancestry individuals, 10,072 East Asian, South Asian and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 3 body fat percentage, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0007800, http://www.ebi.ac.uk/efo/EFO_0004465 GCST011340 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and systolic blood pressure (pairwise) 240,784 European ancestry individuals, 10,072 East Asian, South Asian and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 1 systolic blood pressure, body fat percentage http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0007800 GCST011339 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and coronary artery disease (pairwise) 232,558 European ancestry individuals, 52,463 East Asian, South Asian, Middle Eastern, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 2 body fat percentage, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0007800, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011338 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body fat percentage and type 2 diabetes (pairwise) 200,863 European ancestry individuals, 24,401 East Asian, South Asian and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 11 body fat percentage, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0007800, http://purl.obolibrary.org/obo/MONDO_0005148 GCST011337 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and HDL-C (pairwise) 509,429 European ancestry individuals, 16,962 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 14 body mass index, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004612 GCST011336 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and LDL-C (pairwise) 495,344 European ancestry individuals,16,962 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 5 low density lipoprotein cholesterol measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004340 GCST011335 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and triglycerides (pairwise) 500,123 European ancestry individuals,16,962 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 14 triglyceride measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004340 GCST011334 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and fasting insulin (pairwise) 374,012 European ancestry individuals, 16,962 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 4 body mass index, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004466 GCST011333 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and fasting glucose (pairwise) 380,336 European ancestry individuals, 16,962 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 5 body mass index, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004465 GCST011332 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and systole blood pressure (pairwise) 472,402 European ancestry individuals, 16,962 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 11 systolic blood pressure, body mass index http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004340 GCST011331 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and coronary artery disease (pairwise) 464,176 European ancestry individuals, 59,353 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 6 body mass index, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011330 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Body mass index and type 2 diabetes (pairwise) 418,152 European ancestry individuals, 31,291 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 14 body mass index, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0004340, http://purl.obolibrary.org/obo/MONDO_0005148 GCST011329 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and HDL-C (pairwise) 402,477 European ancestry individuals, 11,333 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 6 waist-hip ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004612 GCST011328 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and LDL-C (pairwise) 388,392 European ancestry individuals, 11,333 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 2 low density lipoprotein cholesterol measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004343 GCST011327 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and triglycerides (pairwise) 393,171 European ancestry individuals, 11,333 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 2 triglyceride measurement, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004343 GCST011326 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and fasting insulin (pairwise) 267,060 European ancestry individuals, 11,333 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 1 waist-hip ratio, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004466 GCST011325 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and fasting glucose (pairwise) 273,384 European ancestry individuals, 11,333 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 1 waist-hip ratio, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004465 GCST011324 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and systolic blood pressure (pairwise) 365,450 European ancestry individuals, 11,333 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 3 systolic blood pressure, waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0004343 GCST011323 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and coronary artery disease (pairwise) 357,224 European ancestry individuals, 53,724 East Asian, South Asian, Middle Eastern, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 1 waist-hip ratio, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0001645 GCST011322 Genome-wide genotyping array 2021-03-22 33619380 Huang LO 2021-02-22 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33619380 Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Waist-hip ratio and type 2 diabetes (pairwise) 311,200 European ancestry individuals, 25,662 East Asian, South Asian, Hispanic and African American ancestry individuals NA Affymetrix, Illumina [2331072] (imputed) 2 waist-hip ratio, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0004343, http://purl.obolibrary.org/obo/MONDO_0005148 GCST011321 Genome-wide genotyping array 2021-02-17 33310728 Ha E 2020-12-11 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33310728 Large-scale meta-analysis across East Asian and European populations updated genetic architecture and variant-driven biology of rheumatoid arthritis, identifying 11 novel susceptibility loci. Rheumatoid arthritis 14,361 European ancestry cases, 43,923 European ancestry controls, 8,267 East Asian ancestry cases, 244,741 East Asian ancestry controls NA NR [13810676] (imputed) 88 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90013534 Genome-wide genotyping array 2021-08-19 33677556 Garnier S 2021-03-03 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/33677556 Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23. Dilated cardiomyopathy 2,651 European ancestry cases, 4,329 European ancestry controls 584 European ancestry cases, 963 European ancestry controls Illumina [9152885] (imputed) 3 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST012211 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T2 FLAIR BIANCA WMH volume 21,381 British ancestry individuals 10,733 British ancestry individuals Affymetrix [17103079] (imputed) 8 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST90003862 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star left thalamus 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003863 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star right thalamus 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003864 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star left caudate 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 17 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003865 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star right caudate 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 18 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003866 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star left putamen 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 20 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003867 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star right putamen 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 20 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003868 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star left pallidum 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 18 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003869 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star right pallidum 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 20 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003870 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star left hippocampus 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003871 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 289) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005142 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 290) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005143 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 291) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005144 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 292) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005145 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 293) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005146 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 294) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005147 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 295) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005148 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 296) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005149 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 297) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005150 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 298) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005151 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 299) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005152 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 300) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005153 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 301) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005154 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 302) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005155 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 303) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005156 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume CA3-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002707 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume HATA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002708 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume Whole-hippocampal-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002709 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume Whole-hippocampal-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002710 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume Whole-hippocampus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002711 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume MGN 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002712 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume LGN 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002713 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume PuI 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002714 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume PuM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002715 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume L-Sg 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002716 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume VPL 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002717 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume CM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002718 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003849 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003850 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003851 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003852 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003853 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003854 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003855 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003856 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003857 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast frontalpole 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003858 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast temporalpole 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003859 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003860 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003861 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002792 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002793 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002794 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002795 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002796 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002797 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002798 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume frontalpole 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002799 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002800 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002801 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002802 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002803 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002804 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh volume cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002805 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star right hippocampus 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003872 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star left amygdala 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003873 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star right amygdala 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003874 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star left accumbens 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003875 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP SWI T2star right accumbens 20,043 British ancestry individuals 10,013 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003876 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Middle cerebellar peduncle 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003877 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Pontine crossing tract 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003878 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Genu of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003879 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Body of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003880 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Splenium of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003881 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS FA Fornix 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90003882 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. Brainstem global volume Midbrain 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002767 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. Brainstem global volume Whole-brainstem 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002768 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002769 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002770 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002771 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002772 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002773 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002774 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002775 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002776 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume isthmuscingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002777 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002778 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume lateralorbitofrontal 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002779 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002780 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002781 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002782 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002783 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002784 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002785 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002786 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002787 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002788 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002789 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002790 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh volume precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002791 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume CM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002742 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume VLa 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002743 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume PuA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002744 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume MDm 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002745 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume Pf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002746 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume VAmc 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002747 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume MDl 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002748 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume VA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002749 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume MV(Re) 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002750 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume CeM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002751 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume VM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002752 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume PuL 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002753 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume CL 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002754 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume VLp 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002755 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume Pc 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002756 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume Pt 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002757 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume AV 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002758 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume LP 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002759 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume LD 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002760 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume LD 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002761 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume Whole-thalamus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002762 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume Whole-thalamus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002763 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. Brainstem global volume Medulla 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002764 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. Brainstem global volume Pons 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 10 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002765 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. Brainstem global volume SCP 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002766 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 379) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005232 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 380) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005233 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume VLa 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002719 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume PuA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002720 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume MDm 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002721 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume Pf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002722 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume VAmc 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002723 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume MDl 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002724 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume CeM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002725 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume VA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002726 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume MV(Re) 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002727 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume VM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002728 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume CL 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002729 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume PuL 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002730 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume Pt 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002731 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume AV 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002732 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume Pc 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002733 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume VLp 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002734 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei lh volume LP 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002735 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume LGN 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002736 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume MGN 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002737 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume PuI 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002738 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume PuM 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002739 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume L-Sg 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002740 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. ThalamNuclei rh volume VPL 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002741 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 304) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005157 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 305) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005158 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 306) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005159 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 307) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005160 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 308) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005161 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 309) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005162 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 310) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005163 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 311) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005164 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 312) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005165 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 313) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005166 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 314) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005167 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 315) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005168 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 316) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005169 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 317) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005170 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 318) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005171 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 319) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005172 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 320) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005173 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 321) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005174 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 322) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005175 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 323) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005176 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 324) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005177 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 325) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005178 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 326) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005179 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 327) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005180 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 328) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005181 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 329) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005182 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 330) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005183 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 331) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005184 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 332) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005185 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 333) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005186 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 334) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005187 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 335) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005188 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 336) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005189 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 337) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005190 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 338) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005191 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 339) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005192 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 340) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005193 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 341) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005194 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 342) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005195 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 343) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005196 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 344) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005197 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 345) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005198 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 346) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005199 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 347) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005200 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 348) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005201 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 349) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005202 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 350) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005203 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 351) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005204 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 352) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005205 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 353) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005206 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 354) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005207 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 355) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005208 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 356) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005209 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 357) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005210 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 358) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005211 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 359) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005212 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 360) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005213 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 361) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005214 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 362) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005215 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 363) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005216 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 364) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005217 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 365) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005218 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 366) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005219 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 367) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005220 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 368) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005221 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 369) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005222 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 370) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005223 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 371) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005224 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 372) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005225 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 373) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005226 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 374) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005227 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 375) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005228 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 376) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005229 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 377) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005230 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 378) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005231 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Fornix cres+Stria terminalis R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004113 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Fornix cres+Stria terminalis L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004114 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior longitudinal fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004115 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior longitudinal fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004116 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior fronto-occipital fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004117 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior fronto-occipital fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004118 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Uncinate fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004119 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Uncinate fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004120 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Tapetum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004121 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Tapetum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004122 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Middle cerebellar peduncle 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004123 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Pontine crossing tract 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004124 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Genu of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004125 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Body of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004126 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Splenium of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004127 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Fornix 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004128 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Corticospinal tract R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004129 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Corticospinal tract L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004130 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Medial lemniscus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004131 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Medial lemniscus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004132 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Inferior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004133 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Inferior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004134 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004135 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004136 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Cerebral peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004137 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004088 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Cerebral peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004089 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Cerebral peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004090 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Anterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004091 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Anterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004092 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Posterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004093 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Posterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004094 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Retrolenticular part of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004095 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Retrolenticular part of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004096 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Anterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004097 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Anterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004098 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004099 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004100 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Posterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004101 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Posterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004102 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Posterior thalamic radiation R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004103 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Posterior thalamic radiation L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004104 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Sagittal stratum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004105 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Sagittal stratum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004106 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 External capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004107 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 External capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004108 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Cingulum cingulate gyrus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004109 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Cingulum cingulate gyrus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004110 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Cingulum hippocampus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004111 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Cingulum hippocampus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004112 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Cerebral peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004138 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Anterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004139 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Anterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004140 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Posterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004141 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Posterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004142 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Retrolenticular part of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004143 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Retrolenticular part of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004144 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Anterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004145 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Anterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004146 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004147 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Superior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004148 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Posterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004149 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Posterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004150 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Posterior thalamic radiation R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004151 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Posterior thalamic radiation L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004152 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Sagittal stratum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004153 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 Sagittal stratum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004154 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 External capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004155 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L2 External capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004156 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-subcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003002 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-transv-frontopol 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003003 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-cingul-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003004 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-cingul-Mid-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003005 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-cingul-Mid-Post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003006 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-cingul-Post-dorsal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003007 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-interm-prim-Jensen 21,259 British ancestry individuals 10,678 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002979 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-intrapariet+P-trans 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002980 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-oc-middle+Lunatus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002981 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-oc-sup+transversal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002982 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-occipital-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002983 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-oc-temp-lat 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002984 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-oc-temp-med+Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002985 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-orbital-lateral 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002986 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-orbital-med-olfact 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002987 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-orbital-H-Shaped 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002988 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-parieto-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002989 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-pericallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002990 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002991 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-precentral-inf-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002992 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-precentral-sup-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002993 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-suborbital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002994 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-subparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002995 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002996 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-temporal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002997 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-temporal-transverse 21,280 British ancestry individuals 10,682 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002998 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-frontomargin 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002999 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-occipital-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003000 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G+S-paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003001 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Cingulum cingulate gyrus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 6 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004061 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Cingulum cingulate gyrus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004062 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Cingulum hippocampus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004063 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Cingulum hippocampus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004064 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Fornix cres+Stria terminalis R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004065 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Fornix cres+Stria terminalis L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004066 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior longitudinal fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004067 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior longitudinal fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004068 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior fronto-occipital fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004069 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior fronto-occipital fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004070 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Uncinate fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004071 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Uncinate fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004072 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Tapetum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004073 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Tapetum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004074 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Middle cerebellar peduncle 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004075 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Pontine crossing tract 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004076 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Genu of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004077 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Body of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004078 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Splenium of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004079 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Fornix 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004080 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Corticospinal tract R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004081 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Corticospinal tract L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004082 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Medial lemniscus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004083 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Medial lemniscus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004084 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Inferior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004085 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Inferior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004086 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L1 Superior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004087 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002904 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002905 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002906 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002907 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002908 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002909 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002910 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume parstriangularis 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002911 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002912 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002913 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002914 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002915 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002916 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002917 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002918 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002919 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002920 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002921 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002922 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002923 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002924 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-frontomargin 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002925 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-occipital-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002926 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002927 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-subcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002928 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-transv-frontopol 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002929 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-cingul-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002930 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-cingul-Mid-Ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002931 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G+S-cingul-Mid-Post 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002932 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-cingul-Post-dorsal 21,280 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002933 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-cingul-Post-ventral 21,279 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002934 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002935 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-front-inf-Opercular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002936 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-front-inf-Orbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002937 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-front-inf-Triangul 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002938 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002939 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002940 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-Ins-lg+S-cent-ins 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002941 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-insular-short 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002942 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-occipital-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002943 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-occipital-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002944 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-oc-temp-lat-fusifor 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002945 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-oc-temp-med-Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002946 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-oc-temp-med-Parahip 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002947 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-orbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002948 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-pariet-inf-Angular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002949 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-pariet-inf-Supramar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002950 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-parietal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002951 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002952 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002953 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-cingul-Post-ventral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003008 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003009 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-front-inf-Opercular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003010 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-front-inf-Orbital 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003011 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-front-inf-Triangul 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003012 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003013 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003014 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-Ins-lg+S-cent-ins 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003015 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-insular-short 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003016 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-occipital-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003017 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-occipital-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003018 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-oc-temp-lat-fusifor 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003019 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-oc-temp-med-Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003020 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-oc-temp-med-Parahip 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003021 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-orbital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003022 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-pariet-inf-Angular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003023 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-pariet-inf-Supramar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003024 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-parietal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003025 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003026 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003027 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003028 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-rectus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003029 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-subcallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003030 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-temp-sup-G-T-transv 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003031 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh volume G-temp-sup-Lateral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90003032 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002954 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-rectus 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002955 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-subcallosal 21,280 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002956 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-temp-sup-G-T-transv 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002957 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-temp-sup-Lateral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002958 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-temp-sup-Plan-polar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002959 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-temp-sup-Plan-tempo 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002960 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002961 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume G-temporal-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002962 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume Lat-Fis-ant-Horizont 21,277 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002963 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume Lat-Fis-ant-Vertical 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002964 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume Lat-Fis-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002965 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume Pole-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002966 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume Pole-temporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002967 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-calcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002968 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002969 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-cingul-Marginalis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002970 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-circular-insula-ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002971 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-circular-insula-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002972 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-circular-insula-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002973 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-collat-transv-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002974 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-collat-transv-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002975 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-front-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002976 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002977 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh volume S-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002978 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 cgh r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004280 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 cst l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004281 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 fma 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004283 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 fmi 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004284 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ifo r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004286 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 mcp 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004289 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ml r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004291 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ptr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004293 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 slf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004294 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 unc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004271 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 unc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004272 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ar l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004273 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ar r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004274 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 atr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004275 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 atr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004276 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 cgc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004277 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 cgc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004278 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 cgh l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004279 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 cst r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004282 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ifo l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004285 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ilf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004287 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ilf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004288 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ml l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004290 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 ptr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004292 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 slf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004295 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003187 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003188 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003189 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003190 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003191 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003192 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003193 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 cgh r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004253 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 cst l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004254 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 cst r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004255 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 fma 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004256 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 fmi 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004257 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ifo l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004258 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ifo r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004259 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ilf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004260 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ilf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004261 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 mcp 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004262 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ml l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004263 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ml r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004264 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ptr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004265 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ptr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004266 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 slf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004267 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 slf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004268 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 str l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004269 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 str r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004270 Genome-wide genotyping array 2021-05-28 33135175 Nicoletti P 2020-11-01 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33135175 Genetic risk factors in drug-induced liver injury due to isoniazid-containing anti-tuberculosis drug regimens. Drug-induced liver injury (isoniazid-containing anti-tuberculosis drugs) 70 European ancestry cases, 10,397 European ancestry controls NA Illumina [at least 4900532] (imputed) 1 response to anti-tuberculosis drug, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007918, http://www.ebi.ac.uk/efo/EFO_0004228 GCST011752 Genome-wide genotyping array 2021-05-28 33135175 Nicoletti P 2020-11-01 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33135175 Genetic risk factors in drug-induced liver injury due to isoniazid-containing anti-tuberculosis drug regimens. Drug-induced liver injury (isoniazid-containing anti-tuberculosis drugs) 55 Indian ancestry cases, 1,199 Indian ancestry controls, 70 European ancestry cases, 10,397 European ancestry controls NA Illumina [4900532] (imputed) 0 response to anti-tuberculosis drug, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007918, http://www.ebi.ac.uk/efo/EFO_0004228 GCST011751 Genome-wide genotyping array 2021-05-28 33135175 Nicoletti P 2020-11-01 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/33135175 Genetic risk factors in drug-induced liver injury due to isoniazid-containing anti-tuberculosis drug regimens. Drug-induced liver injury (isoniazid-containing anti-tuberculosis drugs) 55 Indian ancestry cases, 1,199 Indian ancestry controls NA Illumina [at least 4900532] (imputed) 0 response to anti-tuberculosis drug, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007918, http://www.ebi.ac.uk/efo/EFO_0004228 GCST011753 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior longitudinal fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 11 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004367 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior longitudinal fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 13 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004368 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior fronto-occipital fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004369 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior fronto-occipital fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004370 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Uncinate fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004371 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Uncinate fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004372 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Tapetum R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004373 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Tapetum L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004374 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ar l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004375 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ar r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004376 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF atr l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004377 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF atr r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004378 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF cgc l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004379 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF cgc r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004380 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF cgh l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004381 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF cgh r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004382 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF cst l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004383 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF cst r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004384 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF fma 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004385 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF fmi 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 11 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004386 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ifo l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004387 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ifo r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004388 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ilf l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004389 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ilf r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004390 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF mcp 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004391 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ml l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004392 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ml r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004393 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ptr l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004394 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF ptr r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 12 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004395 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF slf l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 11 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004396 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF slf r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004397 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF str l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004398 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF str r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004399 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF unc l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004400 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ICVF unc r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004401 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Middle cerebellar peduncle 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004402 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Pontine crossing tract 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004403 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Genu of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004404 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Body of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004405 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Splenium of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004406 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Fornix 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004407 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Corticospinal tract R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004408 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Corticospinal tract L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004409 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Medial lemniscus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004410 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Medial lemniscus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004411 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Inferior cerebellar peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004412 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Inferior cerebellar peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004413 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior cerebellar peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004414 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior cerebellar peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004415 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Cerebral peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 6 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004416 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003273 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003274 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003275 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003276 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003277 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003278 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003279 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003280 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003281 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003282 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area parstriangularis 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003283 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003284 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003285 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003286 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003287 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003288 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003289 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003290 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003291 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003292 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003293 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003294 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003295 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh area insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003296 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-frontomargin 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003297 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Cerebral peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004417 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Anterior limb of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004418 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Anterior limb of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004419 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Posterior limb of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004420 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Posterior limb of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004421 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Retrolenticular part of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004422 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Retrolenticular part of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004423 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Anterior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004424 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Anterior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004425 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004426 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004427 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Posterior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004428 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Posterior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004429 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Posterior thalamic radiation R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004430 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Posterior thalamic radiation L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004431 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Sagittal stratum R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004432 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Sagittal stratum L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004433 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD External capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004434 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD External capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004435 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Cingulum cingulate gyrus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004436 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Cingulum cingulate gyrus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004437 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Cingulum hippocampus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004438 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Cingulum hippocampus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004439 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Fornix cres+Stria terminalis R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004440 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Fornix cres+Stria terminalis L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004441 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-occipital-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003298 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003299 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-subcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003300 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-transv-frontopol 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003301 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-cingul-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003302 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-cingul-Mid-Ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003303 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G+S-cingul-Mid-Post 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003304 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-cingul-Post-dorsal 21,280 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003305 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-cingul-Post-ventral 21,279 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003306 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003307 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-front-inf-Opercular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003308 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-front-inf-Orbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003309 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-front-inf-Triangul 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003310 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003311 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003312 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-Ins-lg+S-cent-ins 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003313 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-insular-short 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003314 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-occipital-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003315 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-occipital-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003316 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-oc-temp-lat-fusifor 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003317 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-oc-temp-med-Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003318 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-oc-temp-med-Parahip 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003319 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-orbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003320 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-pariet-inf-Angular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003321 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-pariet-inf-Supramar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003322 Genome-wide genotyping array 2021-03-30 33728380 Fawcett KA 2020-06-01 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/33728380 Variants associated with HHIP expression have sex-differential effects on lung function. FEV1/FVC ratio x sex interaction 168,137 European ancestry women, 135,475 European ancestry men up to 46,911 European and unknown ancestry women, up to 36,258 European and unknown ancestry men Affymetrix [7745864] (imputed) 0 sex interaction measurement, FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004713 GCST90014239 Genome-wide genotyping array 2021-03-30 33728380 Fawcett KA 2020-06-01 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/33728380 Variants associated with HHIP expression have sex-differential effects on lung function. Forced expiratory volume in 1 second x sex interaction 168,137 European ancestry women, 135,475 European ancestry men up to 46,911 European and unknown ancestry women, up to 36,258 European and unknown ancestry men Affymetrix [7745864] (imputed) 0 sex interaction measurement, forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004314 GCST90014240 Genome-wide genotyping array 2021-03-30 33728380 Fawcett KA 2020-06-01 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/33728380 Variants associated with HHIP expression have sex-differential effects on lung function. Forced vital capacity x sex interaction 168,137 European ancestry women, 135,475 European ancestry men up to 46,911 European and unknown ancestry women, up to 36,258 European and unknown ancestry men Affymetrix [7745864] (imputed) 0 sex interaction measurement, vital capacity http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0004312 GCST90014241 Genome-wide genotyping array 2021-03-30 33728380 Fawcett KA 2020-06-01 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/33728380 Variants associated with HHIP expression have sex-differential effects on lung function. Peak expiratory flow x sex interaction 168,137 European ancestry women, 135,475 European ancestry men 24,845 European and unknown ancestry women, 21,208 European and unknown ancestry men Affymetrix [7745864] (imputed) 0 peak expiratory flow, sex interaction measurement http://www.ebi.ac.uk/efo/EFO_0009718, http://www.ebi.ac.uk/efo/EFO_0008343 GCST90014242 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (genus Anaerostipes id.1991) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017127 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (family Bacteroidales S24 7group id.11173) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017128 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (unknown genus id.1000005479) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017129 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota alpha diversity (Inverse Simpson index) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 20 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017130 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota alpha diversity (Shannon index) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 26 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017131 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota alpha diversity (Simpson index) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 23 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017132 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Alloprevotella id.961) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016964 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Anaerofilum id.2053) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016965 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Anaerostipes id.1991) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016966 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Anaerotruncus id.2054) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016967 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Bacteroides id.918) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016968 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Barnesiella id.944) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016969 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Bifidobacterium id.436) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016970 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Bilophila id.3170) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016971 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Blautia id.1992) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016972 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Butyricicoccus id.2055) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016973 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Butyricimonas id.945) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016974 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Butyrivibrio id.1993) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016975 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Candidatus Soleaferrea id.11350) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016976 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Catenibacterium id.2153) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016977 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Christensenellaceae R 7group id.11283) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016978 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Clostridium innocuum group id.14397) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016979 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Clostridium sensustricto1 id.1873) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016980 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Collinsella id.815) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016981 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Coprobacter id.949) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016982 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Methanobacteriales id.120) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017102 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Mollicutes RF9 id.11579) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017103 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order NB1n id.3953) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017104 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Pasteurellales id.3688) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017105 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Rhodospirillales id.2667) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017106 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Selenomonadales id.2165) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017107 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Verrucomicrobiales id.4030) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017108 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (order Victivallales id.2254) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017109 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Actinobacteria id.400) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 13 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017110 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Bacteroidetes id.905) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017111 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Cyanobacteria id.1500) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017112 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Euryarchaeota id.55) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017113 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Firmicutes id.1672) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017114 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Lentisphaerae id.2238) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017115 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Proteobacteria id.2375) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017116 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Tenericutes id.3919) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017117 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (phylum Verrucomicrobia id.3982) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017118 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (genus Turicibacter id.2162) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017119 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (genus Ruminiclostridium6 id.11356) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017120 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (genus Odoribacter id.952) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 15 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017121 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (family Peptococcaceae id.2024) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 19 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017122 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (genus Enterorhabdus id.820) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 18 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017123 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (genus Coprococcus1 id.11301) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 10 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017124 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (family Pseudomonadaceae id.3718) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017125 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota presence (genus Lachnospiraceae UCG 010 id.11330) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 11 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017126 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Actinobacteria id.419) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 14 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016908 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Alphaproteobacteria id.2379) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016909 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Bacilli id.1673) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016910 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Bacteroidia id.912) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016911 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Betaproteobacteria id.2867) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016912 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Clostridia id.1859) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016913 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Coriobacteriia id.809) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016914 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Deltaproteobacteria id.3087) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016915 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Erysipelotrichia id.2147) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016916 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Gammaproteobacteria id.3303) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016917 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Lentisphaeria id.2250) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016918 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Melainabacteria id.1589) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016919 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Methanobacteria id.119) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016920 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Mollicutes id.3920) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016921 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Negativicutes id.2164) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016922 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (class Verrucomicrobiae id.4029) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016923 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Acidaminococcaceae id.2166) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016924 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Actinomycetaceae id.421) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016925 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Alcaligenaceae id.2875) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016926 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Bacteroidaceae id.917) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016927 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Bacteroidales S24 7group id.11173) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016928 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Bifidobacteriaceae id.433) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 16 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016929 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Christensenellaceae id.1866) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016930 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Clostridiaceae1 id.1869) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016931 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (family Clostridiales vadin BB60 group id.11286) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016932 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Coprococcus1 id.11301) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016983 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Coprococcus2 id.11302) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016984 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Coprococcus3 id.11303) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016985 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Defluviitaleaceae UCG011 id.11287) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016986 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Desulfovibrio id.3173) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016987 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Dialister id.2183) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016988 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Dorea id.1997) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016989 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eggerthella id.819) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016990 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eisenbergiella id.11304) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016991 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Enterorhabdus id.820) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016992 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Erysipelatoclostridium id.11381) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 3 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016993 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Erysipelotrichaceae UCG003 id.11384) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016994 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Escherichia Shigella id.3504) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016995 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium brachy group id.11296) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016996 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium coprostanoligenes group id.11375) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016997 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium eligens group id.14372) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016998 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium fissicatena group id.14373) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90016999 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium hallii group id.11338) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017000 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium nodatum group id.11297) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017001 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium oxidoreducens group id.11339) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017002 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium rectale group id.14374) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017003 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium ruminantium group id.11340) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017004 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium ventriosum group id.11341) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017005 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Eubacterium xylanophilum group id.14375) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017006 Genome-wide genotyping array 2021-04-29 33462485 Kurilshikov A 2021-01-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33462485 Large-scale association analyses identify host factors influencing human gut microbiome composition. Gut microbiota abundance (genus Faecalibacterium id.2057) 14,306 European ancestry individuals, 811 Korean ancestry individuals, 1,097 Hispanic individuals, 114 African American individuals, 481 Middle Eastern ancestry individuals, 1,531 unknown and other admixed ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90017007 Genome-wide genotyping array 2018-05-30 29566793 Nicolas A 2018-03-21 Neuron www.ncbi.nlm.nih.gov/pubmed/29566793 Genome-wide Analyses Identify KIF5A as a Novel ALS Gene. Amyotrophic lateral sclerosis 20,806 European ancestry cases, 59,804 European ancestry controls 4,159 cases, 18,650 controls Illumina [10031630] (imputed) 10 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST005647 Genome-wide genotyping array 2020-12-08 32986727 Kalra G 2020-09-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/32986727 Biological insights from multi-omic analysis of 31 genomic risk loci for adult hearing difficulty. Age-related hearing impairment (MTAG) 330,759 European ancestry individuals NA Affymetrix [NR] (imputed) 32 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST90012115 Genome-wide genotyping array 2021-03-30 31150472 Khlebus E 2019-05-31 PLoS One www.ncbi.nlm.nih.gov/pubmed/31150472 Multiple rare and common variants in APOB gene locus associated with oxidatively modified low-density lipoprotein levels. Oxidized LDL cholesterol levels 725 Russian ancestry individuals NA Illumina [101704] 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST011428 Targeted genotyping array [Cardio-MetaboChip] 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 288) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005141 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Lateral-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002633 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Inf-Lat-Vent 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002634 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Cerebellum-White-Matter 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002635 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Cerebellum-Cortex 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002636 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Thalamus-Proper 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002637 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Caudate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002638 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Putamen 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002639 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Pallidum 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002640 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Hippocampus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002641 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Amygdala 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002642 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Accumbens-area 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002643 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume VentralDC 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002644 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume vessel 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002645 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume choroid-plexus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002646 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh number HolesBeforeFixing 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002647 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Lateral-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002648 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Basal-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002649 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Accessory-Basal-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002650 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Anterior-amygdaloid-area-AAA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002651 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Central-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002652 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Medial-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002653 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Cortical-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002654 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Corticoamygdaloid-transitio 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002655 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Paralaminar-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002656 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume CA4-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002682 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume CA4-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002683 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume fimbria 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002684 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume CA3-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002685 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume HATA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002686 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume Whole-hippocampal-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002687 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume Whole-hippocampal-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002688 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume Whole-hippocampus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002689 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume Hippocampal-tail 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002690 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume subiculum-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002691 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume CA1-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002692 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume subiculum-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002693 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume hippocampal-fissure 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002694 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume presubiculum-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002695 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume CA1-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002696 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume presubiculum-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002697 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume parasubiculum 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002698 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume molecular-layer-HP-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002699 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume molecular-layer-HP-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002700 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume GC-ML-DG-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002701 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume CA3-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002702 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume GC-ML-DG-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002703 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume CA4-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002704 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume CA4-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002705 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield rh volume fimbria 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002706 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei lh volume Whole-amygdala 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002657 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Lateral-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002658 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Basal-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002659 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Accessory-Basal-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002660 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Anterior-amygdaloid-area-AAA 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002661 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Central-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002662 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Medial-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002663 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Cortical-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002664 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Corticoamygdaloid-transitio 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002665 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Paralaminar-nucleus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002666 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. AmygNuclei rh volume Whole-amygdala 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002667 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume Hippocampal-tail 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002668 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume subiculum-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002669 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume CA1-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002670 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume subiculum-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002671 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume hippocampal-fissure 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002672 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume presubiculum-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002673 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume CA1-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002674 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume presubiculum-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002675 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume parasubiculum 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002676 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume molecular-layer-HP-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002677 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume molecular-layer-HP-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002678 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume GC-ML-DG-head 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002679 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume CA3-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002680 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. HippSubfield lh volume GC-ML-DG-body 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002681 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 238) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005091 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 239) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005092 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 240) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005093 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 241) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005094 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 242) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005095 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 243) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005096 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 244) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005097 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 245) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005098 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 246) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005099 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 247) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005100 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 248) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005101 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 249) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005102 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 250) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005103 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 251) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005104 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 252) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005105 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 253) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005106 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 254) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005107 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 255) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005108 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 256) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005109 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 257) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005110 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 258) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005111 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 259) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005112 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 260) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005113 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 261) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005114 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 262) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005115 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 263) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005116 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 264) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005117 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 265) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005118 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 266) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005119 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 267) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005120 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 268) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005121 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 269) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005122 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 270) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005123 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 271) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005124 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 272) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005125 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 273) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005126 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 274) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005127 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 275) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005128 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 276) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005129 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 277) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005130 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 278) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005131 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 279) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005132 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 280) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005133 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 281) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005134 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 282) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005135 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 283) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005136 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 284) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005137 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 285) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005138 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 286) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005139 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 287) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005140 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Medial lemniscus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004036 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Inferior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004037 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Inferior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004038 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior cerebellar peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004039 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004040 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Cerebral peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004041 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Cerebral peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004042 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Anterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004043 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Anterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004044 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Posterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004045 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Posterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004046 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Retrolenticular part of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004047 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Retrolenticular part of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004048 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Anterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 6 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004049 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Anterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004050 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004051 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Superior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004052 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Posterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004053 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Posterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004054 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Posterior thalamic radiation R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004055 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Posterior thalamic radiation L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004056 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Sagittal stratum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004057 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Sagittal stratum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004058 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD External capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004059 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD External capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004060 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO fmi 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004011 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ifo l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004012 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ifo r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004013 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ilf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004014 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ilf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004015 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO mcp 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004016 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ml l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004017 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ml r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004018 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ptr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004019 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ptr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004020 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO slf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004021 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO slf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004022 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO str l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004023 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO str r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004024 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO unc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004025 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO unc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004026 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Middle cerebellar peduncle 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004027 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Pontine crossing tract 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004028 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Genu of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004029 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Body of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004030 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Splenium of corpus callosum 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004031 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Fornix 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004032 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Corticospinal tract R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004033 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Corticospinal tract L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004034 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MD Medial lemniscus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004035 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002899 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002900 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002901 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002902 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior cerebellar peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003965 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Cerebral peduncle R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003966 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Cerebral peduncle L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003967 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Anterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003968 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Anterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003969 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Posterior limb of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003970 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Posterior limb of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003971 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Retrolenticular part of internal capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003972 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Retrolenticular part of internal capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003973 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Anterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003974 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Anterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003975 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003976 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003977 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Posterior corona radiata R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003978 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Posterior corona radiata L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003979 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Posterior thalamic radiation R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003980 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Posterior thalamic radiation L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003981 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Sagittal stratum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003982 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Sagittal stratum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003983 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO External capsule R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003984 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO External capsule L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003985 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002874 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002875 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002876 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002877 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002878 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002879 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002880 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002881 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002882 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002883 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002884 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002885 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume rostralanteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002886 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002887 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002888 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002889 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002890 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002891 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002892 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002893 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002894 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002895 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002896 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002897 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002898 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002849 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002850 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA3a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002851 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA3b 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002852 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA4a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002853 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA4p 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002854 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA6 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002855 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA44 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002856 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume BA45 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002857 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume V1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002858 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume V2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002859 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume MT 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002860 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume perirhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002861 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh volume entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002862 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002863 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002864 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002865 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002866 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002867 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002868 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002869 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002870 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002871 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002872 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh volume lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002873 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 481) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005334 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 482) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005335 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 483) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005336 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 484) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005337 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 485) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005338 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 486) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005339 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 487) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005340 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 488) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005341 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 489) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005342 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 490) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005343 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 491) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005344 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 492) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005345 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 493) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005346 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 494) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005347 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 495) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005348 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 496) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005349 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 497) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005350 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 498) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005351 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 499) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005352 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 500) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005353 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 501) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005354 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 502) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005355 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 503) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005356 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 504) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005357 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh volume lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002903 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Cingulum cingulate gyrus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003986 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Cingulum cingulate gyrus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003987 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Cingulum hippocampus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003988 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Cingulum hippocampus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003989 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Fornix cres+Stria terminalis R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003990 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Fornix cres+Stria terminalis L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003991 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior longitudinal fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003992 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior longitudinal fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003993 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior fronto-occipital fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003994 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Superior fronto-occipital fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003995 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Uncinate fasciculus R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003996 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Uncinate fasciculus L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003997 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Tapetum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003998 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS MO Tapetum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003999 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ar l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004000 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO ar r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004001 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO atr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004002 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO atr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004003 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO cgc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004004 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO cgc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004005 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO cgh l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004006 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO cgh r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004007 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO cst l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004008 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO cst r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004009 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MO fma 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004010 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 456) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005309 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 457) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005310 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 458) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005311 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 459) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005312 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 460) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005313 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 461) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005314 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 462) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005315 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 463) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005316 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 464) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005317 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 465) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005318 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 466) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005319 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 467) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005320 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 468) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005321 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 469) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005322 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 470) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005323 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 471) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005324 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 472) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005325 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 473) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005326 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 474) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005327 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 475) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005328 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 476) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005329 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 477) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005330 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 478) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005331 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 479) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005332 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 480) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005333 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 431) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005284 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 432) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005285 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 433) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005286 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 434) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005287 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 435) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005288 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 436) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005289 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 437) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005290 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 438) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005291 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 439) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005292 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 440) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005293 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 441) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005294 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 442) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005295 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 443) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005296 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 444) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005297 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 445) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005298 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 446) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005299 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 447) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005300 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 448) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005301 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 449) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005302 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 450) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005303 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 451) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005304 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 452) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005305 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 453) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005306 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 454) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005307 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 455) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005308 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD str l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004242 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD str r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004243 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD unc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004244 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD unc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004245 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ar l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004246 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 ar r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004247 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 atr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004248 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 atr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004249 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 cgc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004250 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 cgc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004251 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L1 cgh l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004252 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003098 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003099 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003100 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003101 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003102 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003103 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area frontalpole 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003104 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003105 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh area insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003106 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area TotalSurface 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003107 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003108 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003109 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003110 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003111 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003162 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003163 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003164 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003165 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003166 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003167 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003168 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003169 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003170 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003171 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area frontalpole 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003172 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003173 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area TotalSurface 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003174 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003175 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003176 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003177 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003178 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003179 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003180 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003181 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003182 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003183 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003184 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003185 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003186 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003112 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003113 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003114 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003115 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003116 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003117 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003118 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003119 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003120 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003121 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003122 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003123 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003124 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003125 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003126 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003127 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003128 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003129 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003130 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003131 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003132 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003133 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003134 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003135 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003136 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Tapetum R 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004217 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS L3 Tapetum L 20,860 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004218 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ar l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004219 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ar r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004220 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD atr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004221 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD atr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004222 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD cgc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004223 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD cgc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004224 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD cgh l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004225 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD cgh r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004226 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD cst l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004227 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD cst r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004228 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD fma 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004229 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD fmi 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004230 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ifo l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004231 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ifo r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004232 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ilf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004233 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ilf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004234 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD mcp 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004235 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ml l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004236 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ml r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004237 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ptr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004238 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD ptr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004239 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD slf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004240 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX MD slf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004241 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003137 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area frontalpole 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003138 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003139 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh area insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003140 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area TotalSurface 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003141 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003142 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003143 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003144 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003145 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003146 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003147 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003148 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003149 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area isthmuscingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003150 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003151 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area lateralorbitofrontal 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003152 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003153 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003154 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003155 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003156 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003157 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003158 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003159 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003160 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial lh area pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003161 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 slf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004321 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 slf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004322 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 str l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004323 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 str r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004324 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 unc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004325 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 unc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004326 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Middle cerebellar peduncle 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004327 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Pontine crossing tract 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004328 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Genu of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004329 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Body of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004330 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Splenium of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004331 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Fornix 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004332 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Corticospinal tract R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004333 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Corticospinal tract L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004334 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Medial lemniscus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004335 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Medial lemniscus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004336 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Inferior cerebellar peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004337 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Inferior cerebellar peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004338 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior cerebellar peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004339 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Superior cerebellar peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004340 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Cerebral peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 11 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004341 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Cerebral peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004342 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Anterior limb of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004343 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Anterior limb of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004344 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Posterior limb of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004345 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon levels 3,730 Sub-Saharan African ancestry individuals, 1,865 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 1 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90091140 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon levels in lean individuals 1,544 Sub-Saharan African ancestry individuals 601 African American individuals Affymetrix, Illumina [NR] (imputed) 4 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90091172 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon levels 1,510 Sub-Saharan African ancestry men 730 African American men Affymetrix, Illumina [NR] (imputed) 3 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90091153 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon levels in overweight individuals 2,186 Sub-Saharan African ancestry individuals 1,264 African American individuals Affymetrix, Illumina [NR] (imputed) 2 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90091183 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon levels in type 2 diabetes 1,836 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90204157 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon levels 1,894 Sub-Saharan African ancestry individuals 1,658 African American individuals Affymetrix, Illumina [NR] (imputed) 7 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90091195 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon levels 2,220 Sub-Saharan African ancestry women 1,135 African American women Affymetrix, Illumina [NR] (imputed) 1 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90091162 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-10 levels 1,030 Sub-Saharan African ancestry individuals, 886 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 0 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90091145 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-10 levels in lean individuals 1,030 Sub-Saharan African ancestry individuals 886 African American individuals Affymetrix, Illumina [NR] (imputed) 0 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90204161 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-10 levels 381 Sub-Saharan African ancestry men 392 African American men Affymetrix, Illumina [NR] (imputed) 1 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90091151 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-10 levels in overweight individuals 1,030 Sub-Saharan African ancestry individuals 886 African American individuals Affymetrix, Illumina [NR] (imputed) 0 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90204162 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-10 levels in type 2 diabetes 306 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90204163 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-10 levels 724 Sub-Saharan African ancestry individuals 886 African American individuals Affymetrix, Illumina [NR] (imputed) 1 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90091193 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-10 levels 649 Sub-Saharan African ancestry women 494 African American women Affymetrix, Illumina [NR] (imputed) 0 interleukin 10 measurement http://www.ebi.ac.uk/efo/EFO_0004750 GCST90204160 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-1-receptor antagonist levels 780 Sub-Saharan African ancestry individuals 883 African American individuals Affymetrix, Illumina [NR] (imputed) 2 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90091191 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-6 levels 1,263 Sub-Saharan African ancestry individuals, 2,517 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90091139 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-6 levels in lean individuals 520 Sub-Saharan African ancestry individuals 541 African American individuals Affymetrix, Illumina [NR] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90204155 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-6 levels 501 Sub-Saharan African ancestry men 1,146 African American men Affymetrix, Illumina [NR] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90091150 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-6 levels in overweight individuals 743 Sub-Saharan African ancestry individuals 1,976 African American individuals Affymetrix, Illumina [NR] (imputed) 2 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90091181 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-6 levels in type 2 diabetes 564 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90204154 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-6 levels 699 Sub-Saharan African ancestry individuals 2,199 African American individuals Affymetrix, Illumina [NR] (imputed) 1 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90091192 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-6 levels 762 Sub-Saharan African ancestry women 1,371 African American women Affymetrix, Illumina [NR] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90204156 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Glucagon-like peptide-1 levels 2,249 Sub-Saharan African ancestry women 607 African American women Affymetrix, Illumina [NR] (imputed) 0 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90204158 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-1-receptor antagonist levels 1,339 Sub-Saharan African ancestry individuals, 883 African American individuals NA Affymetrix, Illumina [18199418] (imputed) 3 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90091138 Genome-wide genotyping array 2022-12-13 34620218 Meeks KAC 2021-10-07 Genome Med www.ncbi.nlm.nih.gov/pubmed/34620218 Genome-wide analyses of multiple obesity-related cytokines and hormones informs biology of cardiometabolic traits. Interleukin-1-receptor antagonist levels in lean individuals 1,339 Sub-Saharan African ancestry individuals 883 African American individuals Affymetrix, Illumina [NR] (imputed) 0 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90204151 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Posterior limb of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004346 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Retrolenticular part of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 12 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004347 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ICVF Retrolenticular part of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 12 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004348 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003194 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003195 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003196 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003197 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003198 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003199 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003200 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003201 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003202 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003203 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003204 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area frontalpole 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003205 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-pial rh area transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003206 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003207 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003208 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA3a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003209 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA3b 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003210 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA4a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003211 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA4p 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003212 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA6 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003213 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA44 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003214 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area BA45 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003215 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area V1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003216 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area V2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003217 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area MT 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003218 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area perirhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003219 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh area entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003220 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003221 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003222 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA3a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003223 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA3b 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003224 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA4a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003225 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA4p 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003226 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA6 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003227 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA44 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003228 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area BA45 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003229 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area V1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003230 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area V2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003231 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area MT 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003232 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area perirhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003233 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh area entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003234 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003235 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003236 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003237 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003238 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003239 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh area inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003240 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 str l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004296 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 str r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004297 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 unc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004298 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L2 unc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004299 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ar l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004300 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ar r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004301 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 atr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004302 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 atr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004303 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 cgc l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004304 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 cgc r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004305 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 cgh l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004306 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 cgh r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004307 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 cst l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004308 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 cst r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004309 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 fma 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004310 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 fmi 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 8 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004311 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ifo l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 4 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004312 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ifo r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004313 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ilf l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004314 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ilf r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004315 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 mcp 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004316 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ml l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004317 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ml r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004318 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ptr l 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004319 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX L3 ptr r 20,860 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter integrity http://www.ebi.ac.uk/efo/EFO_0004641 GCST90004320 Genome-wide genotyping array 2021-07-23 33499410 Liao YH 2021-01-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/33499410 Functional Haplotype of LIPC Induces Triglyceride-Mediated Suppression of HDL-C Levels According to Genome-Wide Association Studies. High density lipoprotein cholesterol levels 4,000 East Asian ancestry individuals NA Affymetrix [614821] 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST012045 Genome-wide genotyping array 2020-04-17 30572963 Marquez A 2018-12-20 Genome Med www.ncbi.nlm.nih.gov/pubmed/30572963 Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. Autoimmune traits (pleiotropy) 11,489 European ancestry cases with celiac disease, 15,523 European ancestry cases with rheumatoid arthritis, 3,477 European ancestry cases with systemic sclerosis, 6,670 European ancestry cases with type 1 diabetes, 22,308 European ancestry controls NA Illumina [252970] 38 autoimmune disease http://www.ebi.ac.uk/efo/EFO_0005140 GCST009873 Targeted genotyping array [ImmunoChip] 2020-04-17 30572963 Marquez A 2018-12-20 Genome Med www.ncbi.nlm.nih.gov/pubmed/30572963 Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. Celiac disease 11,489 European ancestry cases, 22,308 European ancestry controls NA Illumina [252970] 35 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST009874 Targeted genotyping array [ImmunoChip] 2020-04-17 30572963 Marquez A 2018-12-20 Genome Med www.ncbi.nlm.nih.gov/pubmed/30572963 Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. Type 1 diabetes 6,670 European ancestry cases, 22,308 European ancestry controls NA Illumina [252970] 26 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST009875 Targeted genotyping array [ImmunoChip] 2020-04-17 30572963 Marquez A 2018-12-20 Genome Med www.ncbi.nlm.nih.gov/pubmed/30572963 Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. Rheumatoid arthritis 15,523 European ancestry cases, 22,308 European ancestry controls NA Illumina [252970] 24 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST009877 Targeted genotyping array 2020-04-17 30572963 Marquez A 2018-12-20 Genome Med www.ncbi.nlm.nih.gov/pubmed/30572963 Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations. Systemic sclerosis 3,477 European ancestry cases, 22,308 European ancestry controls NA Illumina [252970] 9 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST009876 Targeted genotyping array [ImmunoChip] 2020-03-30 31959851 Olafsdottir TA 2020-01-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31959851 Eighty-eight variants highlight the role of T cell regulation and airway remodeling in asthma pathogenesis. Asthma 16,247 European ancestry cases, 346,486 European ancestry controls, 52,942 cases, 355,713 controls NA Affymetrix [32463443] (imputed) 88 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST009798 Genome-wide genotyping array 2020-02-20 31886626 Hettema JM 2019-12-30 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/31886626 Genome-wide association study of shared liability to anxiety disorders in Army STARRS. Anxiety disorder (factor score) 28,950 European ancestry individuals, 2,482 African American individuals, 3,264 Latino individuals NA Illumina [up to 10000000] (imputed) 2 anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0007795 GCST009679 Genome-wide genotyping array 2020-03-31 31959275 Micalizzi L 2020-01-21 Dev Psychopathol www.ncbi.nlm.nih.gov/pubmed/31959275 Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth. Attention deficit hyperactivity disorder (inattention symptoms) 3,563 European ancestry children and adolescents NA Illumina [5360405] (imputed) 7 ADHD symptom measurement http://www.ebi.ac.uk/efo/EFO_0007860 GCST009812 Genome-wide genotyping array 2021-05-18 33296963 Brugger SW 2020-10-04 Mult Scler Relat Disord www.ncbi.nlm.nih.gov/pubmed/33296963 Depression in multiple sclerosis patients associated with risk variant near NEGR1. Depression in multiple sclerosis (pre-diagnosis) 27 European ancestry cases, 1,180 European ancestry controls NA Illumina [602644] 4 unipolar depression, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0005301 GCST011679 Genome-wide genotyping array 2021-05-18 33296963 Brugger SW 2020-10-04 Mult Scler Relat Disord www.ncbi.nlm.nih.gov/pubmed/33296963 Depression in multiple sclerosis patients associated with risk variant near NEGR1. Depression in multiple sclerosis (post-diagnosis) 130 European ancestry cases, 1,180 European ancestry controls NA Illumina [602644] 2 unipolar depression, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0005301 GCST011678 Genome-wide genotyping array 2021-05-18 33296963 Brugger SW 2020-10-04 Mult Scler Relat Disord www.ncbi.nlm.nih.gov/pubmed/33296963 Depression in multiple sclerosis patients associated with risk variant near NEGR1. Depression in multiple sclerosis 182 European ancestry cases, 1,180 European ancestry controls NA Illumina [602644] 2 unipolar depression, multiple sclerosis http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0005301 GCST011680 Genome-wide genotyping array 2021-08-20 33654092 Shigemizu D 2021-03-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33654092 Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk. Alzheimer's disease 3,962 Japanese ancestry cases, 4,074 Japanese ancestry controls 1,216 Japanese ancestry cases, 2,446 Japanese ancestry controls Affymetrix [4852957] (imputed) 3 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST012215 Genome-wide genotyping array 2021-08-20 33654092 Shigemizu D 2021-03-03 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33654092 Ethnic and trans-ethnic genome-wide association studies identify new loci influencing Japanese Alzheimer's disease risk. Alzheimer's disease 3,962 Japanese ancestry cases, 4,074 Japanese ancestry controls, 21,982 European ancestry cases, 41,944 European ancestry controls 1,216 Japanese ancestry cases, 2,446 Japanese ancestry controls Affymetrix [2067592] (imputed) 8 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST012214 Genome-wide genotyping array 2018-07-09 28706201 Wei WH 2017-07-13 Sci Rep www.ncbi.nlm.nih.gov/pubmed/28706201 Genotypic variability based association identifies novel non-additive loci DHCR7 and IRF4 in sero-negative rheumatoid arthritis. Sero-negative rheumatoid arthritis 3,323 European ancestry cases, 15,785 European ancestry controls NA Illumina [107144] 2 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST005826 Targeted genotyping array [ImmunoChip] 2022-10-21 33669802 Park S 2021-02-19 Int J Environ Res Public Health www.ncbi.nlm.nih.gov/pubmed/33669802 Menopause, Ultraviolet Exposure, and Low Water Intake Potentially Interact with the Genetic Variants Related to Collagen Metabolism Involved in Skin Wrinkle Risk in Middle-Aged Women. Facial wrinkles 77 Korean ancestry wrinkled cases, 51 Korean ancestry less wrinkled controls NA Affymetrix [NR] (imputed) 0 Facial wrinkling http://purl.obolibrary.org/obo/HP_0009762 GCST013040 Genome-wide genotyping array 2021-08-26 33654266 Bonelli R 2021-03-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33654266 Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder. Macular telangiectasia type 2 1,067 European or unknown ancestry cases, 3,799 European or unknown ancestry controls NA Illumina [7289516] (imputed) 17 macular telangiectasia type 2 http://www.ebi.ac.uk/efo/EFO_1002009 GCST012252 Genome-wide genotyping array 2021-08-26 33654266 Bonelli R 2021-03-02 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33654266 Identification of genetic factors influencing metabolic dysregulation and retinal support for MacTel, a retinal disorder. Macular telangiectasia type 2 931 European ancestry cases, 3,745 European ancestry controls NA Illumina [7289516] (imputed) 17 macular telangiectasia type 2 http://www.ebi.ac.uk/efo/EFO_1002009 GCST012251 Genome-wide genotyping array 2018-07-06 29562276 Venkateswaran S 2018-03-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/29562276 Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis. Childhood onset ulcerative colitis 466 European ancestry cases, 2,099 European ancestry controls NA Affymetrix [3996700] (imputed) 4 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST005815 Genome-wide genotyping array 2021-07-29 33501934 Suzuki K 2021-01-27 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/33501934 Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease. Diarrhea in mesalamine-treated irritable bowel disease 86 Japanese ancestry cases, 1,437 Japanese ancestry controls 23 Japanese ancestry cases, 765 Japanese ancestry controls NR [7215020] (imputed) 2 Diarrhea, response to sulfasalazine http://purl.obolibrary.org/obo/HP_0002014, http://www.ebi.ac.uk/efo/EFO_0008324 GCST012153 Genome-wide genotyping array 2021-07-29 33501934 Suzuki K 2021-01-27 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/33501934 Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease. Fever in mesalamine-treated irritable bowel disease 90 Japanese ancestry cases, 1,433 Japanese ancestry controls 22 Japanese ancestry cases, 766 Japanese ancestry controls NR [7215020] (imputed) 4 Fever, response to sulfasalazine http://purl.obolibrary.org/obo/HP_0001945, http://www.ebi.ac.uk/efo/EFO_0008324 GCST012152 Genome-wide genotyping array 2021-07-29 33501934 Suzuki K 2021-01-27 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/33501934 Genetic Background of Mesalamine-induced Fever and Diarrhea in Japanese Patients with Inflammatory Bowel Disease. Fever and diarrhea in mesalamine-treated irritable bowel disease 49 Japanese ancestry cases, 1,474 Japanese ancestry controls 14 Japanese ancestry cases, 774 Japanese ancestry controls NR [7215020] (imputed) 3 Fever, Diarrhea, response to sulfasalazine http://purl.obolibrary.org/obo/HP_0001945, http://purl.obolibrary.org/obo/HP_0002014, http://www.ebi.ac.uk/efo/EFO_0008324 GCST012154 Genome-wide genotyping array 2018-05-02 29559957 Wang W 2018-03-06 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/29559957 Heritability and Genome-Wide Association Analyses of Serum Uric Acid in Middle and Old-Aged Chinese Twins. Serum uric acid levels 139 Chinese ancestry dizygotic twin pairs NA Illumina [1365181] 7 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST005557 Genome-wide genotyping array 2019-08-05 31123309 Rayner C 2019-05-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31123309 A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders. Response to cognitive-behavioural therapy in anxiety and major depressive disorders 972 European ancestry adult anxiety disorder cases, 832 adult major depressive disorder cases, 920 child anxiety disorder cases NA Illumina [4710000] (imputed) 3 cognitive behavioural therapy http://www.ebi.ac.uk/efo/EFO_0007820 GCST008358 Genome-wide genotyping array 2019-08-05 31123309 Rayner C 2019-05-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31123309 A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders. Response to cognitive-behavioural therapy in anxiety disorder 920 child cases NA Illumina [at least 4710000] (imputed) 10 cognitive behavioural therapy http://www.ebi.ac.uk/efo/EFO_0007820 GCST008359 Genome-wide genotyping array 2019-08-05 31123309 Rayner C 2019-05-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31123309 A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders. Response to cognitive-behavioural therapy in anxiety disorder 972 European ancestry adult cases NA Illumina [at least 4710000] (imputed) 6 cognitive behavioural therapy http://www.ebi.ac.uk/efo/EFO_0007820 GCST008360 Genome-wide genotyping array 2019-08-05 31123309 Rayner C 2019-05-23 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/31123309 A genome-wide association meta-analysis of prognostic outcomes following cognitive behavioural therapy in individuals with anxiety and depressive disorders. Response to cognitive-behavioural therapy in major depressive disorder 832 adult cases NA Illumina [at least 4710000] (imputed) 9 cognitive behavioural therapy http://www.ebi.ac.uk/efo/EFO_0007820 GCST008361 Genome-wide genotyping array 2019-03-27 30552108 Kawabata Y 2018-12-14 Diabetes www.ncbi.nlm.nih.gov/pubmed/30552108 A genome-Wide Association Study Confirming a Strong Effect of HLA and Identifying Variants in CSAD/lnc-ITGB7-1 on Chromosome 12q13.13 Associated with Susceptibility to Fulminant Type 1 Diabetes. Fulminant type 1 diabetes 257 Japanese ancestry cases, 419 Japanese ancestry controls NA Affymetrix [426851] (imputed) 9 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST007433 Genome-wide genotyping array 2021-03-28 31134134 Hollister BM 2019-05-10 Front Genet www.ncbi.nlm.nih.gov/pubmed/31134134 A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population. Systolic blood pressure 2,577 African American Individuals NA Illumina [115834] 3 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011424 Targeted genotyping array [Metabochip] 2021-03-28 31134134 Hollister BM 2019-05-10 Front Genet www.ncbi.nlm.nih.gov/pubmed/31134134 A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population. Diastolic blood pressure 2,577 African American Individuals NA Illumina [115834] 2 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011423 Targeted genotyping array [Metabochip] 2021-03-28 31134134 Hollister BM 2019-05-10 Front Genet www.ncbi.nlm.nih.gov/pubmed/31134134 A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population. Systolic blood pressure (education interaction) 1,518 African American individuals with high school education, 731 African American individuals with college education, 328 African American individuals with less than high school education NA Illumina [115834] 3 educational attainment, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0011015, http://www.ebi.ac.uk/efo/EFO_0006335 GCST011422 Targeted genotyping array [Metabochip] 2021-03-28 31134134 Hollister BM 2019-05-10 Front Genet www.ncbi.nlm.nih.gov/pubmed/31134134 A Social Determinant of Health May Modify Genetic Associations for Blood Pressure: Evidence From a SNP by Education Interaction in an African American Population. Diastolic blood pressure (education interaction) 1,518 African American individuals with high school education, 731 African American individuals with college education, 328 African American individuals with less than high school education NA Illumina [115834] 2 educational attainment, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0011015, http://www.ebi.ac.uk/efo/EFO_0006336 GCST011421 Targeted genotyping array [Metabochip] 2019-10-24 31135556 Wyles CC 2019-05-13 Clin Orthop Relat Res www.ncbi.nlm.nih.gov/pubmed/31135556 CORR® ORS Richard A. Brand Award: Disruption in Peroxisome Proliferator-Activated Receptor-γ (PPARG) Increases Osteonecrosis Risk Through Genetic Variance and Pharmacologic Modulation. Idiopathic osteonecrosis of the femoral head 3 African American cases, 1 Asian ancestry case, 98 European ancestry cases, 6 African American controls, 1 Asian ancestry control, 4,118 European ancestry controls 1 African American case, 1 Asian ancestry case, 36 European ancestry cases, 1 African American control, 2 Asian ancestry controls, 461 European ancestry controls Illumina [NR] (imputed) 1 idiopathic osteonecrosis of the femoral head http://www.ebi.ac.uk/efo/EFO_1001930 GCST008913 Genome-wide genotyping array 2019-07-25 31127053 Tang Y 2019-05-24 Diabetes www.ncbi.nlm.nih.gov/pubmed/31127053 A Genetic Locus on Chromosome 2q24 Predicting Peripheral Neuropathy Risk in Type 2 Diabetes: Results From the ACCORD and BARI 2D Studies. Diabetic peripheral neuropathy in type 2 diabetes 4,384 European ancestry cases, 784 European ancestry controls 791 European ancestry cases, 158 European ancestry controls, 1,345 African American individuals Affymetrix, Illumina [6847206] (imputed) 5 peripheral neuropathy http://www.ebi.ac.uk/efo/EFO_0003100 GCST008223 Genome-wide genotyping array 2019-02-27 30531935 Crowley JJ 2018-12-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30531935 Common-variant associations with fragile X syndrome. Fragile X syndrome 80 European ancestry male cases, 9 male cases, 266 European ancestry male controls NA Illumina [750000] 1 fragile X syndrome http://purl.obolibrary.org/obo/MONDO_0010383 GCST007233 Genome-wide genotyping array 2018-07-05 29559738 Sasayama D 2018-03-20 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29559738 A genome-wide association study on photic sneeze syndrome in a Japanese population. Photic sneeze reflex 360 Japanese ancestry cases, 11,049 Japanese ancestry controls NA Illumina [210086] 3 autosomal dominant compelling helio-ophthalmic outburst syndrome http://www.ebi.ac.uk/efo/EFO_0007887 GCST005809 Genome-wide genotyping array 2019-02-06 30552173 Aterido A 2018-12-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/30552173 Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis. Psoriatic arthritis 744 Spanish ancestry cases, 1,454 Spanish ancestry controls 1,430 cases, 1,417 controls Illumina [1387382] (imputed) 38 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST007043 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (primary open-angle) 16,677 European ancestry cases, 199,580 European ancestry controls 7,286 European ancestry cases, 107,362 European ancestry controls, 6,935 East Asian ancestry cases, 39,588 East Asian ancestry controls, 3,281 Sub-Saharan African ancestry cases, 2,791 Sub-Saharan African ancestry controls Affymetrix, Illumina [14822926] (imputed) 23 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90011766 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (primary open-angle) 15,229 European ancestry cases, 177,473 European ancestry controls NA Affymetrix, Illumina [12971527] (imputed) 0 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90011767 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (primary open-angle) 6,935 East Asian ancestry cases, 39,588 East Asian ancestry controls NA Illumina [11610548] (imputed) 23 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90011768 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (primary open-angle) 3,281 Sub-Saharan African ancestry cases, 2,791 Sub-Saharan African ancestry controls NA Illumina [16121080] (imputed) 1 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90011769 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (primary open-angle) 23,963 European ancestry cases, 306,942 European ancestry controls, 6,935 East Asian ancestry cases, 39,588 East Asian ancestry controls, 3,281 Sub-Saharan African ancestry cases, 2,791 Sub-Saharan African ancestry controls 43,254 European ancestry cases, 1,471,118 European ancestry controls Illumina [15409056] (imputed) 88 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90011770 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (high intraocular pressure) 3,376 European ancestry cases, 15,151 European ancestry controls, 1,516 East Asian ancestry cases, 32,649 East Asian ancestry controls, 252 Sub-Saharan African ancestry cases, 197 Sub-Saharan African ancestry controls NA Illumina [NR] (imputed) 13 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST011441 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (low intraocular pressure) 1,886 European ancestry cases, 15,151 European ancestry controls, 1,315 East Asian ancestry cases, 32,649 East Asian ancestry controls, 46 Sub-Saharan African ancestry cases, 197 Sub-Saharan African ancestry controls NA Illumina [NR] (imputed) 6 low tension glaucoma http://www.ebi.ac.uk/efo/EFO_1001022 GCST011440 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (primary open-angle) 8,758 European ancestry cases, 108,815 European ancestry controls, 1,996 East Asian ancestry cases, 16,559 East Asian ancestry controls, 171 Sub-Saharan African ancestry cases, 94 Sub-Saharan African ancestry controls NA Illumina [NR] (imputed) 30 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST011439 Genome-wide genotyping array 2021-03-31 33627673 Gharahkhani P 2021-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33627673 Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries. Glaucoma (primary open-angle) 9,179 European ancestry cases, 134,471 European ancestry controls, 1,983 East Asian ancestry cases, 13,719 East Asian ancestry controls, 127 Sub-Saharan African ancestry cases, 100 Sub-Saharan African ancestry controls NA Illumina [NR] (imputed) 32 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST011438 Genome-wide genotyping array 2021-07-28 33495599 Johnson N 2021-01-26 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/33495599 CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers. Estrone-3-glucuronide levels 560 European ancestry individuals NA Illumina [8280353] (imputed) 1 estrone conjugate measurement http://www.ebi.ac.uk/efo/EFO_0007971 GCST012151 Genome-wide genotyping array 2021-07-28 33495599 Johnson N 2021-01-26 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/33495599 CYP3A7*1C allele: linking premenopausal oestrone and progesterone levels with risk of hormone receptor-positive breast cancers. Pregnanediol-3-glucuronide levels 560 European ancestry individuals NA Illumina [8280353] (imputed) 0 sex hormone measurement http://www.ebi.ac.uk/efo/EFO_0011008 GCST012150 Genome-wide genotyping array 2021-08-13 33691233 Peterson RE 2021-02-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/33691233 Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium. smoking initiation in schizophrenia 5,255 European ancestry individuals 1,802 East Asian individuals NR [9500000] (imputed) 4 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST012181 Genome-wide genotyping array 2021-08-13 33691233 Peterson RE 2021-02-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/33691233 Genome-wide analyses of smoking behaviors in schizophrenia: Findings from the Psychiatric Genomics Consortium. Cigarettes smoked per day in Schizophrenia 3,370 European ancestry individuals 1,802 East Asian individuals NR [9500000] (imputed) 5 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST012180 Genome-wide genotyping array 2021-03-22 33578652 Adjei AA 2021-02-10 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/33578652 Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach. Mental health related quality of life 1,386 European ancestry individuals, 56 individuals NA Illumina [7254516] (imputed) 5 health-related quality of life measurement http://www.ebi.ac.uk/efo/EFO_0011014 GCST011362 Genome-wide genotyping array 2021-03-22 33578652 Adjei AA 2021-02-10 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/33578652 Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach. Physical health related quality of life 1,386 European ancestry individuals, 56 individuals NA Illumina [7254516] (imputed) 2 health-related quality of life measurement http://www.ebi.ac.uk/efo/EFO_0011014 GCST011361 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Posterior limb of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004495 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Posterior limb of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004496 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Retrolenticular part of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004497 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Retrolenticular part of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004498 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Anterior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004499 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Anterior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004500 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004501 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004502 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Posterior corona radiata R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004503 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Posterior corona radiata L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004504 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Posterior thalamic radiation R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004505 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Posterior thalamic radiation L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004506 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Sagittal stratum R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004507 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Sagittal stratum L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004508 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF External capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004509 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF External capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004510 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Cingulum cingulate gyrus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004511 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Cingulum cingulate gyrus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004512 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Cingulum hippocampus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004513 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Cingulum hippocampus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004514 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Fornix cres+Stria terminalis R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004515 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Fornix cres+Stria terminalis L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004516 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior longitudinal fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004517 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior longitudinal fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004518 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior fronto-occipital fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004519 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-front-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003348 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003349 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003350 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-interm-prim-Jensen 21,259 British ancestry individuals 10,678 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003351 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-intrapariet+P-trans 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003352 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-oc-middle+Lunatus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003353 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-oc-sup+transversal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003354 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-occipital-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003355 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-oc-temp-lat 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003356 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-oc-temp-med+Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003357 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-orbital-lateral 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003358 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-orbital-med-olfact 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003359 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-orbital-H-Shaped 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003360 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-parieto-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003361 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-pericallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003362 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003363 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-precentral-inf-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003364 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-precentral-sup-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003365 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-suborbital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003366 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-subparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003367 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003368 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-temporal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003369 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior longitudinal fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004442 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior longitudinal fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004443 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior fronto-occipital fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004444 Genome-wide genotyping array 2021-11-24 34621292 Sampathkumar A 2021-09-21 Front Genet www.ncbi.nlm.nih.gov/pubmed/34621292 Genetic Link Determining the Maternal-Fetal Circulation of Vitamin D. Neonatal total 25-hydroxyvitamin D levels (cord blood) up to 399 Chinese ancestry neonates, up to 166 Indian ancestry neonates, up to 247 Malay ancestry neonates NA Illumina [6978879] (imputed) 1 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90053840 Genome-wide genotyping array 2021-11-24 34621292 Sampathkumar A 2021-09-21 Front Genet www.ncbi.nlm.nih.gov/pubmed/34621292 Genetic Link Determining the Maternal-Fetal Circulation of Vitamin D. Midgestational total 25-hydroxyvitamin D levels (antenatal blood) up to 520 Chinese ancestry pregnant female individuals, up to 175 Indian ancestry pregnant female individuals, up to 247 Malay ancestry pregnant female individuals NA Illumina [6978879] (imputed) 2 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90053839 Genome-wide genotyping array 2021-10-13 34020725 Reddy JS 2021-05-21 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/34020725 Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease. Cerebral amyloid angiopathy in APOEe4 carrier Alzheimer’s disease 534 European ancestry individuals NA Illumina [1679420] (imputed) 1 cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0006790 GCST012482 Genome-wide genotyping array 2021-10-13 34020725 Reddy JS 2021-05-21 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/34020725 Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease. Cerebral amyloid angiopathy in APOEe4 non-carrier Alzheimer’s disease 287 European ancestry individuals NA Illumina [1679420] (imputed) 5 cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0006790 GCST012483 Genome-wide genotyping array 2021-10-13 34020725 Reddy JS 2021-05-21 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/34020725 Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease. Cerebral amyloid angiopathy x sex interaction in Alzheimer’s disease 370 European ancestry men, 451 European ancestry women NA Illumina [1679420] (imputed) 15 sex interaction measurement, cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0006790 GCST012485 Genome-wide genotyping array 2021-10-13 34020725 Reddy JS 2021-05-21 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/34020725 Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease. Cerebral amyloid angiopathy x APOEe4 status interaction in Alzheimer’s disease 534 European ancestry APOEe4 carriers, 287 European ancestry APOEe4 non-carriers NA Illumina [1679420] (imputed) 25 APOE carrier status, cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0007659, http://www.ebi.ac.uk/efo/EFO_0006790 GCST012484 Genome-wide genotyping array 2021-10-13 34020725 Reddy JS 2021-05-21 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/34020725 Genome-wide analysis identifies a novel LINC-PINT splice variant associated with vascular amyloid pathology in Alzheimer's disease. Cerebral amyloid angiopathy in Alzheimer’s disease 821 European ancestry individuals NA Illumina [1679420] (imputed) 16 cerebral amyloid angiopathy http://www.ebi.ac.uk/efo/EFO_0006790 GCST012481 Genome-wide genotyping array 2021-10-20 34304350 Lim WY 2021-07-25 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34304350 Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome. Insulin levels 4,658 Korean ancestry females NA Affymetrix [NR] (imputed) 13 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90027075 Genome-wide genotyping array 2021-10-20 34304350 Lim WY 2021-07-25 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34304350 Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome. Insulin levels 4,182 Korean ancestry male NA Affymetrix [NR] (imputed) 13 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90027076 Genome-wide genotyping array 2021-10-20 34304350 Lim WY 2021-07-25 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34304350 Identification of genetic variants for blood insulin level in sex-stratified Korean population and evaluation of the causal relationship between blood insulin level and polycystic ovary syndrome. Insulin levels 4,658 Korean ancestry females, 4,182 Korean ancestry males NA Affymetrix [NR] (imputed) 6 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90027077 Genome-wide genotyping array 2021-10-26 34417442 Cheng S 2021-08-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34417442 Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. Alcohol consumption x experiences in childhood (felt loved by family member) interaction 41,648 European ancestry individuals NA Affymetrix [NR] (imputed) 60 wellbeing measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007869, http://www.ebi.ac.uk/efo/EFO_0007878 GCST90032654 Genome-wide genotyping array 2021-10-26 34417442 Cheng S 2021-08-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34417442 Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. Alcohol consumption x traumatic event in childhood (felt hated by family member) interaction 46,394 European ancestry individuals NA Affymetrix [NR] (imputed) 36 childhood trauma measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007979, http://www.ebi.ac.uk/efo/EFO_0007878 GCST90032655 Genome-wide genotyping array 2021-10-26 34417442 Cheng S 2021-08-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34417442 Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. Alcohol consumption x traumatic event in childhood (sexually molested) interaction 47,598 European ancestry individuals NA Affymetrix [NR] (imputed) 0 childhood trauma measurement, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007979, http://www.ebi.ac.uk/efo/EFO_0007878 GCST90032656 Genome-wide genotyping array 2021-10-26 34417442 Cheng S 2021-08-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34417442 Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. Smoking x experiences in childhood (felt loved by family member) interaction 11,465 European ancestry individuals NA Affymetrix [NR] (imputed) 5 wellbeing measurement, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007869, http://www.ebi.ac.uk/efo/EFO_0005671 GCST90032657 Genome-wide genotyping array 2021-10-26 34417442 Cheng S 2021-08-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34417442 Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. Smoking x traumatic event in childhood (felt hated by family member) interaction 124,481 European ancestry individuals NA Affymetrix [NR] (imputed) 4 childhood trauma measurement, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007979, http://www.ebi.ac.uk/efo/EFO_0005671 GCST90032658 Genome-wide genotyping array 2021-10-26 34417442 Cheng S 2021-08-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34417442 Traumatic events during childhood and its risks to substance use in adulthood: an observational and genome-wide by environment interaction study in UK Biobank. Smoking x traumatic event in childhood (sexually molested) interaction 127,766 European ancestry individuals NA Affymetrix [NR] (imputed) 29 childhood trauma measurement, smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0007979, http://www.ebi.ac.uk/efo/EFO_0005671 GCST90032659 Genome-wide genotyping array 2022-02-03 34276655 Wen S 2021-07-01 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34276655 Identification of Two Novel Candidate Genetic Variants Associated With the Responsiveness to Influenza Vaccination. Response to influenza vaccine 34 Chinese ancestry responders, 77 Chinese ancestry non-responders 193 Chinese ancestry responders, 288 Chinese ancestry non-responders NR [13013995] 1 response to vaccine http://www.ebi.ac.uk/efo/EFO_0004645 GCST90093368 Genome-wide sequencing 2021-10-04 34064523 Rodrigo LM 2021-05-04 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34064523 Imputation and Reanalysis of ExomeChip Data Identifies Novel, Conditional and Joint Genetic Effects on Parkinson's Disease Risk. Parkinson's disease 5,167 European ancestry cases, 5,366 European ancestry controls NA Illumina [1465938] (imputed) 14 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST012431 Genome-wide genotyping array 2023-02-23 36800424 Sha Z 2023-02-17 Sci Adv www.ncbi.nlm.nih.gov/pubmed/36800424 Genetic architecture of the white matter connectome of the human brain. Node-level brain connectivity (multivariate analysis) 30,810 British ancestry individuals NA NR [9312361] (imputed) 140 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90165317 Genome-wide genotyping array 2023-02-23 36800424 Sha Z 2023-02-17 Sci Adv www.ncbi.nlm.nih.gov/pubmed/36800424 Genetic architecture of the white matter connectome of the human brain. Edge-level brain connectivity (multivariate analysis) 30,810 British ancestry individuals NA NR [9312361] (imputed) 211 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90165318 Genome-wide genotyping array 2021-10-27 34197731 Li Q 2021-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34197731 Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia. Idiopathic achalasia 280 Chinese Han ancestry cases, 1,121 Chinese Han ancestry controls NA Illumina [476650] (imputed) 2 Achalasia http://purl.obolibrary.org/obo/HP_0002571 GCST90025934 Genome-wide genotyping array 2021-10-27 34197731 Li Q 2021-06-23 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34197731 Whole-exome sequencing reveals common and rare variants in immunologic and neurological genes implicated in achalasia. Idiopathic achalasia 100 Chinese Han ancestry cases, 313 Chinese Han ancestry controls 230 Chinese Han ancestry cases, 1,760 Chinese Han ancestry controls Illumina [192329] 2 Achalasia http://purl.obolibrary.org/obo/HP_0002571 GCST90025935 Genome-wide sequencing 2021-10-25 34220922 Wang J 2021-06-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34220922 Genome-Wide Association Analyses Identify Variants in IRF4 Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility. Acute myeloid leukemia or myelodysplastic syndrome (pleiotropy) 1,769 European ancestry acute myeloid leukemia cases, 540 myelodysplastic syndrome cases, 2,814 European ancestry controls NA Illumina [9000000] (imputed) 1 acute myeloid leukemia, myelodysplastic syndrome http://www.ebi.ac.uk/efo/EFO_0000222, http://www.ebi.ac.uk/efo/EFO_0000198 GCST90020096 Genome-wide genotyping array 2021-10-25 34220922 Wang J 2021-06-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34220922 Genome-Wide Association Analyses Identify Variants in IRF4 Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility. Therapy-related myelodysplastic syndrome 96 European ancestry cases, 2,814 European ancestry controls NA Illumina [9000000] (imputed) 1 myelodysplastic syndrome http://www.ebi.ac.uk/efo/EFO_0000198 GCST90020097 Genome-wide genotyping array 2021-10-25 34220922 Wang J 2021-06-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34220922 Genome-Wide Association Analyses Identify Variants in IRF4 Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility. De novo myelodysplastic syndrome 444 European ancestry cases, 2,814 European ancestry controls NA Illumina [9000000] (imputed) 0 myelodysplastic syndrome http://www.ebi.ac.uk/efo/EFO_0000198 GCST90020098 Genome-wide genotyping array 2021-10-25 34220922 Wang J 2021-06-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34220922 Genome-Wide Association Analyses Identify Variants in IRF4 Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility. Therapy-related acute myeloid leukemia 146 European ancestry cases, 2,814 European ancestry controls NA Illumina [9000000] (imputed) 0 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST90054800 Genome-wide genotyping array 2021-10-25 34220922 Wang J 2021-06-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34220922 Genome-Wide Association Analyses Identify Variants in IRF4 Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility. De novo acute myeloid leukemia (normal cytogenetics) 543 European ancestry cases, 2,814 European ancestry controls NA Illumina [9000000] (imputed) 0 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST90054801 Genome-wide genotyping array 2021-10-25 34220922 Wang J 2021-06-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34220922 Genome-Wide Association Analyses Identify Variants in IRF4 Associated With Acute Myeloid Leukemia and Myelodysplastic Syndrome Susceptibility. De novo acute myeloid leukemia (abnormal cytogenetics) 836 European ancestry cases, 2,814 European ancestry controls NA Illumina [9000000] (imputed) 0 acute myeloid leukemia http://www.ebi.ac.uk/efo/EFO_0000222 GCST90054802 Genome-wide genotyping array 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Height 6,044 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90013304 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Body mass index 6,039 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90013305 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Calcium levels 6,020 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90013306 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Chloride levels 6,018 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 chloride measurement http://www.ebi.ac.uk/efo/EFO_0009284 GCST90013307 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Iron levels 6,010 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006332 GCST90013308 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Magnesium levels 5,996 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST90013309 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Potassium levels 6,017 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 potassium measurement http://www.ebi.ac.uk/efo/EFO_0009283 GCST90013310 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Sodium levels 6,018 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST90013311 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Bicarbonate levels 6,017 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 blood bicarbonate measurement http://www.ebi.ac.uk/efo/EFO_0011012 GCST90013312 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Serum alkaline phosphatase levels 6,012 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90013313 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Alanine aminotransferase levels 6,018 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90013314 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Aspartate aminotransferase levels 6,018 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90013315 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Creatine kinase levels 5,344 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST90013316 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Gamma glutamyl transferase levels 4,650 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90013317 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Activated partial thromboplastin time 5,988 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 partial thromboplastin time http://www.ebi.ac.uk/efo/EFO_0004310 GCST90013318 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Prothrombin time 5,989 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 1 prothrombin time measurement http://www.ebi.ac.uk/efo/EFO_0008390 GCST90013319 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. International normalisation ratio 5,987 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 1 prothrombin time measurement http://www.ebi.ac.uk/efo/EFO_0008390 GCST90013320 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Fibrinogen levels 5,984 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90013321 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. White blood cell count 6,007 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 5 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90013322 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Red blood cell count 6,007 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90013323 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Sitting height 6,034 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 sitting height measurement http://www.ebi.ac.uk/efo/EFO_0011011 GCST90013303 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Mean corpuscular hemoglobin concentration 6,007 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90013324 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Mean corpuscular hemoglobin 6,007 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90013325 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Mean corpuscular volume 6,007 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90013326 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Platelet count 5,935 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90013327 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Mean platelet volume 6,006 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90013328 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Hematocrit 6,007 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90013329 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Hemoglobin 6,006 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90013330 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Total cholesterol levels 6,017 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90013331 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. High density lipoprotein cholesterol levels 6,013 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90013332 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Low density lipoprotein cholesterol levels 5,972 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90013333 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Triglycerides 6,017 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90013334 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Serum total protein levels 6,017 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90013335 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Serum albumin levels 6,018 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90013336 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Ferritin levels 5,947 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90013337 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. C-peptide levels 5,925 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 C-peptide measurement http://www.ebi.ac.uk/efo/EFO_0005187 GCST90013338 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Pro B-type natriuretic peptide 5,516 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90013339 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Iron status biomarkers (total iron binding capacity) 6,010 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 total iron binding capacity http://www.ebi.ac.uk/efo/EFO_0006334 GCST90013340 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Unsaturated iron binding capacity 5,956 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST90013341 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Total bilirubin levels 6,018 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 3 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90013342 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Uric acid levels 6,013 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880615] 1 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90013343 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Serum folate levels 5,944 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 red blood cell folate measurement http://www.ebi.ac.uk/efo/EFO_0009703 GCST90013344 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Serum creatinine levels 6,018 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90013345 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Homocysteine levels 5,727 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 3 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST90013346 Genome-wide sequencing [NA] 2021-12-14 33623009 Thareja G 2021-02-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33623009 Whole genome sequencing in the Middle Eastern Qatari population identifies genetic associations with 45 clinically relevant traits. Vitamin B12 levels 5,865 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Illumina [7880617] 1 vitamin B12 measurement http://www.ebi.ac.uk/efo/EFO_0004620 GCST90013347 Genome-wide sequencing [NA] 2022-10-21 33633223 Park JH 2021-02-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33633223 Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes. Remission after SSRI treatment in major depression 36 Korean ancestry cases, 64 Korean ancestry controls 185 Korean ancestry cases, 368 Korean ancestry controls Illumina [13318214] 0 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST90093291 Genome-wide sequencing 2022-10-21 33633223 Park JH 2021-02-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33633223 Whole-genome sequencing reveals KRTAP1-1 as a novel genetic variant associated with antidepressant treatment outcomes. Response to selective serotonin reuptake inhibitors in depression 60 Korean ancestry cases, 40 Korean ancestry controls 299 Korean ancestry cases, 254 Korean ancestry controls Illumina [13318214] 0 response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0005658 GCST90093292 Genome-wide sequencing 2021-11-03 34523824 Lakshman Kumar P 2021-09-15 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/34523824 Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease. Weight loss in chronic obstructive pulmonary disease 1,380 non-Hispanic White ancestry individuals 2,389 non-Hispanic White ancestry individuals Illumina [5405435] (imputed) 2 body weight loss http://www.ebi.ac.uk/efo/EFO_0005245 GCST90044906 Genome-wide genotyping array 2021-11-03 34523824 Lakshman Kumar P 2021-09-15 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/34523824 Genetic variation in genes regulating skeletal muscle regeneration and tissue remodelling associated with weight loss in chronic obstructive pulmonary disease. Weight loss in chronic obstructive pulmonary disease 401 African American individuals 138 African American individuals Illumina [7629332] (imputed) 7 body weight loss http://www.ebi.ac.uk/efo/EFO_0005245 GCST90044907 Genome-wide genotyping array 2022-01-07 34518958 Sanders AR 2021-09-13 Arch Sex Behav www.ncbi.nlm.nih.gov/pubmed/34518958 Genome-Wide Linkage and Association Study of Childhood Gender Nonconformity in Males. Childhood gender nonconformity 409 European ancestry concordant male sibling pairs NA Affymetrix [6030650] (imputed) 27 childhood gender nonconformity http://www.ebi.ac.uk/efo/EFO_0020103 GCST90044896 Genome-wide genotyping array 2021-11-08 34604815 Polfus LM 2021-03-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34604815 Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Type 2 diabetes 29,832 European ancestry cases, 147,369 European ancestry controls, 8,591 African American, African ancestry cases, 16,887 African American African ancestry controls, 3,124 Asian ancestry cases, 4,313 Asian ancestry controls, 1,642 Oceanian ancestry cases, 2,152 Oceanian ancestry controls, 9,913 Hispanic or Latin American cases, 22,958 Hispanic or Latin American controls 109,274 European ancestry cases, 154,346 European ancestry controls, 20,344 African American, African ancestry cases, 97,933 African American, African ancestry controls, 2,237 East Asian ancestry cases, 72,819 East Asian ancestry controls, 1,171 South Asian ancestry cases, 18,874 South Asian ancestry controls, 77,418 Asian ancestry cases, 356,122 Asian ancestry controls, 20,608 Hispanic or Latin American cases, 246,046 Hispanic or Latin American controls Affymetrix, Illumina [NR] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90053824 Genome-wide genotyping array 2021-11-08 34604815 Polfus LM 2021-03-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34604815 Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Type 2 diabetes 8,591 African American, African ancestry cases, 16,887 African American, African ancestry controls 20,344 African American, African ancestry cases, 97,933 African American, African ancestry controls Affymetrix, Illumina [NR] (imputed) 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90053830 Genome-wide genotyping array 2021-11-08 34604815 Polfus LM 2021-03-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34604815 Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Type 2 diabetes 3,124 Asian ancestry cases, 4,313 Asian ancestry controls 2,237 East Asian ancestry cases, 72,819 East Asian ancestry controls, 1,171 South Asian ancestry cases, 18,874 South Asian ancestry controls, 77,418 Asian ancestry cases, 356,122 Asian ancestry controls Illumina [NR] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90053826 Genome-wide genotyping array 2021-11-08 34604815 Polfus LM 2021-03-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34604815 Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Type 2 diabetes 1,642 Native Hawaiian ancestry cases, 2,152 Native Hawaiian ancestry controls NA Illumina [NR] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90053827 Genome-wide genotyping array 2021-11-08 34604815 Polfus LM 2021-03-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34604815 Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Type 2 diabetes 29,832 European ancestry cases, 147,369 European ancestry controls 109,274 European ancestry cases, 154,346 European ancestry controls Affymetrix, Illumina [NR] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90053828 Genome-wide genotyping array 2021-11-08 34604815 Polfus LM 2021-03-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/34604815 Genetic discovery and risk characterization in type 2 diabetes across diverse populations. Type 2 diabetes 9,913 Hispanic or Latin American cases, 22,958 Hispanic or Latin American controls 20,608 Hispanic or Latin American cases, 246,046 Hispanic or Latin American controls Illumina [NR] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90053829 Genome-wide genotyping array 2021-10-21 34390503 Yang G 2021-08-14 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/34390503 Genome-wide Association Study Identified Chromosome 8 Locus Associated with Medication-related Osteonecrosis of the Jaw. Bisphosphonate-related osteonecrosis of the jaw in cancer (i.v. bisphosphonate) 217 European ancestry cases, 2,208 European ancestry controls 109 European ancestry cases, 1,105 European ancestry controls Illumina [126146] (imputed) 3 response to bisphosphonate, osteonecrosis http://www.ebi.ac.uk/efo/EFO_0009958, http://www.ebi.ac.uk/efo/EFO_0004259 GCST90027893 Genome-wide genotyping array 2021-10-21 34390503 Yang G 2021-08-14 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/34390503 Genome-wide Association Study Identified Chromosome 8 Locus Associated with Medication-related Osteonecrosis of the Jaw. Bisphosphonate-related osteonecrosis of the jaw in osteoporosis (oral bisphosphonate) 118 European ancestry cases, 1,251 European ancestry controls NA Illumina [126146] (imputed) 3 response to bisphosphonate, osteonecrosis http://www.ebi.ac.uk/efo/EFO_0009958, http://www.ebi.ac.uk/efo/EFO_0004259 GCST90027894 Genome-wide genotyping array 2021-10-21 34390503 Yang G 2021-08-14 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/34390503 Genome-wide Association Study Identified Chromosome 8 Locus Associated with Medication-related Osteonecrosis of the Jaw. Bisphosphonate-related osteonecrosis of the jaw 444 European ancestry cases, 4,564 European ancestry controls NA Illumina [126146] (imputed) 2 response to bisphosphonate, osteonecrosis http://www.ebi.ac.uk/efo/EFO_0009958, http://www.ebi.ac.uk/efo/EFO_0004259 GCST90053855 Genome-wide genotyping array 2021-11-05 34518561 Urbanek ME 2021-09-13 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34518561 Genetic predisposition to tinnitus in the UK Biobank population. Tinnitus (chronic, bothersome) 300 female European ancestry cases, 11,732 female European ancestry controls NA IDT xGen Exome Sequencing Research Panel v1.0 8 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90044891 Exome-wide sequencing [IDT xGen Exome Sequencing Research Panel v1.0] 2021-11-05 34518561 Urbanek ME 2021-09-13 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34518561 Genetic predisposition to tinnitus in the UK Biobank population. Tinnitus (chronic, bothersome) 226 male European ancestry cases, 7,315 male European ancestry controls NA IDT xGen Exome Sequencing Research Panel v1.0 10 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90044892 Exome-wide sequencing [IDT xGen Exome Sequencing Research Panel v1.0] 2022-01-31 33910581 Zhuang Z 2021-04-29 BMC Med www.ncbi.nlm.nih.gov/pubmed/33910581 Shared genetic etiology and causality between body fat percentage and cardiovascular diseases: a large-scale genome-wide cross-trait analysis. Body fat percentage or coronary artery disease (MTAG) 89,297 European ancestry individuals with body fat percentage, 11,419 Korean ancestry, Indian ancestry, Jamaican ancestry individuals with body fat percentage, 61,289 European ancestry, East Asian ancestry, South Asian ancestry, African American, Hispanic cases with coronary artery disease, 134,524 European ancestry, East Asian ancestry, South Asian ancestry, African American, Hispanic controls without coronary artery disease NA NR [NR] (imputed) 16 body fat percentage, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0007800, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90085924 Genome-wide genotyping array 2022-02-21 33910581 Zhuang Z 2021-04-29 BMC Med www.ncbi.nlm.nih.gov/pubmed/33910581 Shared genetic etiology and causality between body fat percentage and cardiovascular diseases: a large-scale genome-wide cross-trait analysis. Body fat percentage or heart failure (MTAG) 89,297 European ancestry individuals with body fat percentage, 47,309 European ancestry cases with heart failure, 930,014 European ancestry controls without heart failure, 11,419 Korean ancestry, Indian Asian ancestry, Jamaican ancestry individuals with body fat percentage NA NR [NR] (imputed) 5 heart failure, body fat percentage http://www.ebi.ac.uk/efo/EFO_0003144, http://www.ebi.ac.uk/efo/EFO_0007800 GCST90085925 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Cardiorespiratory fitness (vo2 max) 70,783 European ancestry individuals NA Affymetrix [8918919] (imputed) 12 maximal oxygen uptake measurement http://www.ebi.ac.uk/efo/EFO_0004887 GCST90093316 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Cardiorespiratory fitness (vo2 max) 34,419 European ancestry men NA Affymetrix [8918919] (imputed) 4 maximal oxygen uptake measurement http://www.ebi.ac.uk/efo/EFO_0004887 GCST90093317 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Cardiorespiratory fitness (vo2 max) 36,364 European ancestry women NA Affymetrix [8918919] (imputed) 0 maximal oxygen uptake measurement http://www.ebi.ac.uk/efo/EFO_0004887 GCST90093318 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Cardiorespiratory fitness slope 70,783 European ancestry individuals NA Affymetrix [8918919] (imputed) 8 heart rate response to exercise http://www.ebi.ac.uk/efo/EFO_0009184 GCST90093319 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Cardiorespiratory fitness slope 34,419 European ancestry men NA Affymetrix [8918919] (imputed) 2 heart rate response to exercise http://www.ebi.ac.uk/efo/EFO_0009184 GCST90093320 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Cardiorespiratory fitness slope 36,364 European ancestry women NA Affymetrix [8918919] (imputed) 1 heart rate response to exercise http://www.ebi.ac.uk/efo/EFO_0009184 GCST90093321 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Physical activity 89,683 European ancestry individuals NA Affymetrix [8918919] (imputed) 9 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90093322 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Physical activity 39,352 European ancestry men NA Affymetrix [8918919] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90093323 Genome-wide genotyping array 2022-02-01 34753499 Hanscombe KB 2021-11-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/34753499 The genetic case for cardiorespiratory fitness as a clinical vital sign and the routine prescription of physical activity in healthcare. Physical activity 50,331 European ancestry women NA Affymetrix [8918919] (imputed) 4 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90093324 Genome-wide genotyping array 2022-02-02 34929384 Mekki Y 2021-12-17 Neuroimage www.ncbi.nlm.nih.gov/pubmed/34929384 The genetic architecture of language functional connectivity. Language functional connectivity 32,186 British ancestry individuals NA Affymetrix [9812367] (imputed) 20 functional brain measurement, language measurement http://www.ebi.ac.uk/efo/EFO_0007849, http://www.ebi.ac.uk/efo/EFO_0007797 GCST90093325 Genome-wide genotyping array 2022-02-02 34929384 Mekki Y 2021-12-17 Neuroimage www.ncbi.nlm.nih.gov/pubmed/34929384 The genetic architecture of language functional connectivity. Language functional connectivity 4,754 non British ancestry individuals NA Affymetrix [9812367] (imputed) 0 functional brain measurement, language measurement http://www.ebi.ac.uk/efo/EFO_0007849, http://www.ebi.ac.uk/efo/EFO_0007797 GCST90093326 Genome-wide genotyping array 2022-02-03 35046404 Chou WC 2022-01-19 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/35046404 A common variant in 11q23.3 associated with hyperlipidemia is mediated by the binding and regulation of GATA4. Hyperlipidemia 3,310 Taiwanese ancestry cases, 6,404 Taiwanese ancestry controls 829 Taiwanese ancestry cases, 1,833 Taiwanese ancestry controls Affymetrix [597758] 5 hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0021187 GCST90090994 Genome-wide genotyping array 2021-11-02 34446935 Karlsson Linner R 2021-08-26 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34446935 Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. Externalizing behaviour (multivariate analysis) up to 53,293 European ancestry Attention-deficit/hyperactivity disorder individuals, up to 164,684 European ancestry problematic alcohol use individuals, up to 186,875 European ancestry lifetime cannabis use individuals, up to 357,187 European ancestry individuals measuring reverse-coded age at first sexual intercourse, up to 336,121 European ancestry individuals measuring number of sexual partners, up to 426,379 European ancestry individuals measuring general risk tolerance, up to 1,251,809 European ancestry individuals measuring lifetime smoking initiation NA NR [NR] (imputed) 579 attention deficit hyperactivity disorder, substance abuse, antisocial behaviour measurement http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0002491, http://www.ebi.ac.uk/efo/EFO_0007052 GCST90061435 Genome-wide genotyping array 2023-02-23 36792583 Albinana C 2023-02-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36792583 Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots. 25-Hydroxyvitamin D levels 64,988 European ancestry individuals NA Illumina [6091695] (imputed) 1 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90162562 Genome-wide genotyping array 2023-02-23 36792583 Albinana C 2023-02-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36792583 Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots. Vitamin D-binding protein levels 65,589 European ancestry individuals NA Illumina [6091695] (imputed) 26 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST90162563 Genome-wide genotyping array 2023-02-23 36792583 Albinana C 2023-02-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36792583 Genetic correlates of vitamin D-binding protein and 25-hydroxyvitamin D in neonatal dried blood spots. Vitamin D-binding protein levels (adjusted for GC haplotype) 65,590 European ancestry individuals NA Illumina [6091695] (imputed) 15 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST90162564 Genome-wide genotyping array 2021-12-14 32399468 Melhuish Beaupre LM 2020-01-08 Mol Neuropsychiatry www.ncbi.nlm.nih.gov/pubmed/32399468 Genome-Wide Association Study of Sleep Disturbances in Depressive Disorders. Sleep disturbance (changes in sleep) in depressive disorders 36 European ancestry cases, 329 European ancestry controls NA Illumina [5932083] (imputed) 13 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST90085921 Genome-wide genotyping array 2021-12-14 32399468 Melhuish Beaupre LM 2020-01-08 Mol Neuropsychiatry www.ncbi.nlm.nih.gov/pubmed/32399468 Genome-Wide Association Study of Sleep Disturbances in Depressive Disorders. Sleep disturbance (increased sleep) in depressive disorders 128 European ancestry cases, 223 European ancestry controls NA Illumina [5932083] (imputed) 21 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST90085922 Genome-wide genotyping array 2021-12-14 32399468 Melhuish Beaupre LM 2020-01-08 Mol Neuropsychiatry www.ncbi.nlm.nih.gov/pubmed/32399468 Genome-Wide Association Study of Sleep Disturbances in Depressive Disorders. Sleep disturbance (decreased sleep) in depressive disorders 144 European ancestry cases, 219 European ancestry controls NA Illumina [5932083] (imputed) 10 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST90085923 Genome-wide genotyping array 2021-11-05 33888571 Lee S 2021-04-22 Thorax www.ncbi.nlm.nih.gov/pubmed/33888571 Novel recessive locus for body mass index in childhood asthma. Body mass index in childhood asthma 892 Hispanic or Latin American trios 216 European ancestry trios, 28 African American trios, 19 Latin American trios, 23 trios NR [8689950] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90052899 Genome-wide sequencing 2021-11-05 33888571 Lee S 2021-04-22 Thorax www.ncbi.nlm.nih.gov/pubmed/33888571 Novel recessive locus for body mass index in childhood asthma. Body mass index in childhood asthma 892 Hispanic or Latin American trios 216 European ancestry trios, 28 African American trios, 19 Latin American ancestry trios, 23 trios NR [8689950] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90052900 Genome-wide sequencing 2022-01-06 34753797 Riveros-Mckay F 2021-11-09 Diabetes www.ncbi.nlm.nih.gov/pubmed/34753797 An Expanded Genome-Wide Association Study of Fructosamine Levels Identifies RCN3 as a Replicating Locus and Implicates FCGRT as the Effector Transcript. Fructosamine levels 20,731 European ancestry individuals NA Affymetrix [19100024] (imputed) 2 fructosamine measurement http://www.ebi.ac.uk/efo/EFO_0009303 GCST90017143 Genome-wide genotyping array 2022-01-06 34753797 Riveros-Mckay F 2021-11-09 Diabetes www.ncbi.nlm.nih.gov/pubmed/34753797 An Expanded Genome-Wide Association Study of Fructosamine Levels Identifies RCN3 as a Replicating Locus and Implicates FCGRT as the Effector Transcript. Fructosamine levels 20,731 European ancestry individuals 7,647 European ancestry individuals Affymetrix [19100024] (imputed) 3 fructosamine measurement http://www.ebi.ac.uk/efo/EFO_0009303 GCST012619 Genome-wide genotyping array 2022-01-26 35023831 Chong M 2022-01-13 Elife www.ncbi.nlm.nih.gov/pubmed/35023831 GWAS and ExWAS of blood Mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia. Mitochondrial DNA copy number 395,718 British, Irish, Other White, South Asian, African ancestry individuals NA Affymetrix [23037915] (imputed) 73 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90026371 Genome-wide genotyping array 2022-01-26 35023831 Chong M 2022-01-13 Elife www.ncbi.nlm.nih.gov/pubmed/35023831 GWAS and ExWAS of blood Mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia. Mitochondrial DNA copy number 383,476 British, Irish, Other White ancestry individuals NA Affymetrix [11453766] (imputed) 0 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90026372 Genome-wide genotyping array 2022-01-26 35023831 Chong M 2022-01-13 Elife www.ncbi.nlm.nih.gov/pubmed/35023831 GWAS and ExWAS of blood Mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia. Mitochondrial DNA copy number 6,172 South Asian ancestry individuals NA Affymetrix [11350981] (imputed) 0 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90026373 Genome-wide genotyping array 2022-01-26 35023831 Chong M 2022-01-13 Elife www.ncbi.nlm.nih.gov/pubmed/35023831 GWAS and ExWAS of blood Mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia. Mitochondrial DNA copy number 6,133 African ancestry individuals NA Affymetrix [18981896] (imputed) 0 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90026374 Genome-wide genotyping array 2022-02-01 34671089 Hikino K 2021-10-21 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34671089 Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer. Colorectal cancer 6,845 East Asian ancestry cases, 80,764 East Asian ancestry controls NA Illumina [NR] (imputed) 11 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90093302 Genome-wide genotyping array 2022-02-01 34671089 Hikino K 2021-10-21 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34671089 Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer. Colorectal polyp 4,447 East Asian ancestry cases, 157,226 East Asian ancestry controls NA Illumina [8624880] (imputed) 1 polyp of large intestine http://purl.obolibrary.org/obo/MONDO_0021392 GCST90093301 Genome-wide genotyping array 2022-02-01 34671089 Hikino K 2021-10-21 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34671089 Genome-wide association study of colorectal polyps identified highly overlapping polygenic architecture with colorectal cancer. Colorectal polyp and colorectal cancer (MTAG) 11,292 East Asian ancestry cases, 237,990 East Asian ancestry controls NA Illumina [NR] (imputed) 17 polyp of large intestine, colorectal cancer http://purl.obolibrary.org/obo/MONDO_0021392, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90093303 Genome-wide genotyping array 2022-01-28 34268393 Xu JY 2021-05-01 Ann Transl Med www.ncbi.nlm.nih.gov/pubmed/34268393 Nucleotide polymorphism in ARDS outcome: a whole exome sequencing association study. Survival in acute respiratory distress syndrome 70 cases, 35 controls NA Illumina [471131] 0 survival time, acute respiratory distress syndrome http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000637 GCST90093314 Exome-wide sequencing 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Disease-related mortality after unrelated donor allogeneic hematopoietic cell transplantation (recipient effect) 2,799 European ancestry recipients with acute myeloid leukemia or myelodysplastic syndrome NA Illumina [8515276] (imputed) 0 response to allogeneic hematopoietic stem cell transplant, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092524 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Disease-related mortality after unrelated donor allogeneic hematopoietic cell transplantation (donor effect) 2,799 European ancestry donors NA Illumina [8515276] (imputed) 4 response to allogeneic hematopoietic stem cell transplant, donor genotype effect measurement, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0007892, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092525 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Disease-related mortality after unrelated donor allogeneic hematopoietic cell transplantation (donor-recipient mismatch) 2,799 European ancestry donor-recipient pairs NA Illumina [8515276] (imputed) 0 response to allogeneic hematopoietic stem cell transplant, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092526 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Mortality after unrelated donor allogeneic hematopoietic cell transplantation (recipient effect) 2,799 European ancestry recipients NA Illumina [8515276] (imputed) 1 response to allogeneic hematopoietic stem cell transplant, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092518 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Mortality after unrelated donor allogeneic hematopoietic cell transplantation (donor effect) 2,799 European ancestry donors NA Illumina [8515276] (imputed) 0 response to allogeneic hematopoietic stem cell transplant, donor genotype effect measurement, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0007892, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092519 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Mortality after unrelated donor allogeneic hematopoietic cell transplantation (donor-recipient mismatch) 2,799 European ancestry donor-recipient pairs NA Illumina [8515276] (imputed) 1 response to allogeneic hematopoietic stem cell transplant, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092520 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Transplant-related mortality after unrelated donor allogeneic hematopoietic cell transplantation (recipient effect) 2,799 European ancestry recipients NA Illumina [8515276] (imputed) 1 response to allogeneic hematopoietic stem cell transplant, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092521 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Transplant-related mortality after unrelated donor allogeneic hematopoietic cell transplantation (donor effect) 2,799 European ancestry donors NA Illumina [8515276] (imputed) 0 response to allogeneic hematopoietic stem cell transplant, donor genotype effect measurement, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0007892, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092522 Genome-wide genotyping array 2022-01-10 34746714 Hahn T 2021-08-25 EClinicalMedicine www.ncbi.nlm.nih.gov/pubmed/34746714 Novel genetic variants associated with mortality after unrelated donor allogeneic hematopoietic cell transplantation. Transplant-related mortality after unrelated donor allogeneic hematopoietic cell transplantation (donor-recipient mismatch) 2,799 European ancestry donor-recipient pairs NA Illumina [8515276] (imputed) 1 response to allogeneic hematopoietic stem cell transplant, mortality http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90092523 Genome-wide genotyping array 2021-11-19 34563919 Chiba Y 2021-09-20 J Neurol Sci www.ncbi.nlm.nih.gov/pubmed/34563919 Genetic and demographic predisposing factors associated with pediatric sleepwalking in the Philadelphia Neurodevelopmental Cohort. Sleepwalking 155 African American cases, 2,598 African American controls NA Illumina [NR] (imputed) 5 Somnambulism http://purl.obolibrary.org/obo/HP_0025236 GCST90053831 Genome-wide genotyping array 2021-11-19 34563919 Chiba Y 2021-09-20 J Neurol Sci www.ncbi.nlm.nih.gov/pubmed/34563919 Genetic and demographic predisposing factors associated with pediatric sleepwalking in the Philadelphia Neurodevelopmental Cohort. Sleepwalking 512 European ancestry cases, 4,250 European ancestry controls NA Illumina [NR] (imputed) 2 Somnambulism http://purl.obolibrary.org/obo/HP_0025236 GCST90053832 Genome-wide genotyping array 2021-11-19 34563919 Chiba Y 2021-09-20 J Neurol Sci www.ncbi.nlm.nih.gov/pubmed/34563919 Genetic and demographic predisposing factors associated with pediatric sleepwalking in the Philadelphia Neurodevelopmental Cohort. Sleepwalking 155 African American cases, 2,598 African American controls, 512 European ancestry cases, 4,250 European ancestry controls NA Illumina [NR] (imputed) 2 Somnambulism http://purl.obolibrary.org/obo/HP_0025236 GCST90053833 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER negative treated with chemotherapy) 6,852 European ancestry individuals NA NR [10000000] (imputed) 1 estrogen-receptor negative breast cancer, survival time, breast carcinoma, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305, http://purl.obolibrary.org/obo/GO_0097327 GCST90029046 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER positive, PR positive, and HER2 negative) 35,550 European ancestry individuals NA NR [10000000] (imputed) 1 survival time, estrogen-receptor positive breast cancer, breast carcinoma, HER2 negative breast carcinoma, progesterone-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0009780, http://www.ebi.ac.uk/efo/EFO_0009782 GCST90029047 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER positive or PR positive, and HER2 negative treated with chemotherapy) 10,394 European ancestry individuals NA NR [10000000] (imputed) 1 survival time, estrogen-receptor positive breast cancer, breast carcinoma, HER2 negative breast carcinoma, progesterone-receptor positive breast cancer, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0009780, http://www.ebi.ac.uk/efo/EFO_0009782, http://purl.obolibrary.org/obo/GO_0097327 GCST90029048 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER positive or PR positive, and HER2 negative not treated with chemotherapy) 10,275 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, estrogen-receptor positive breast cancer, breast carcinoma, HER2 negative breast carcinoma, progesterone-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0009780, http://www.ebi.ac.uk/efo/EFO_0009782 GCST90029049 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER positive or PR positive, and HER2 positive) 5,567 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, HER2 Positive Breast Carcinoma, estrogen-receptor positive breast cancer, breast carcinoma, progesterone-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000294, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0009782 GCST90029050 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER negative or PR negative, and HER2 positive) 2,298 European ancestry individuals NA NR [10000000] (imputed) 0 progesterone-receptor negative breast cancer, estrogen-receptor negative breast cancer, survival time, HER2 Positive Breast Carcinoma, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0009781, http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000294, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029051 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER negative or PR negative, and HER2 negative) 5,631 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, breast carcinoma, triple-negative breast cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0005537 GCST90029052 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (treated with tamoxifen) 17,327 European ancestry individuals NA NR [10000000] (imputed) 0 response to tamoxifen, survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0009391, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029053 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (treated with aromatase inhibitor) 9,041 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, response to aromatase inhibitor, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/GO_0061477, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029054 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (treated with Cyclophosphamide Methotrexate Fluorouracil (CMF)-like chemotherapy regimen) 2,663 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, response to combination chemotherapy, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0007965, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029055 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (treated with taxane) 5,545 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, breast carcinoma, response to taxane http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0008580 GCST90029056 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (treated with anthracyclines) 11,183 European ancestry individuals NA NR [10000000] (imputed) 1 survival time, breast carcinoma, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0005257 GCST90029057 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (ER positive treated with endocrine therapy) 27,340 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, estrogen-receptor positive breast cancer, breast carcinoma, response to endocrine therapy http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0007613 GCST90029058 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (ER negative treated with chemotherapy) 6,411 European ancestry individuals NA NR [10000000] (imputed) 2 estrogen-receptor negative breast cancer, survival time, breast carcinoma, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305, http://purl.obolibrary.org/obo/GO_0097327 GCST90029059 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (ER positive or PR positive, and HER2 negative treated with chemotherapy) 10,273 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, estrogen-receptor positive breast cancer, breast carcinoma, HER2 negative breast carcinoma, progesterone-receptor positive breast cancer, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0009780, http://www.ebi.ac.uk/efo/EFO_0009782, http://purl.obolibrary.org/obo/GO_0097327 GCST90029060 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (ER positive or PR positive, and HER2 negative not treated with chemotherapy) 10,156 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, estrogen-receptor positive breast cancer, breast carcinoma, HER2 negative breast carcinoma, progesterone-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0009780, http://www.ebi.ac.uk/efo/EFO_0009782 GCST90029061 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (treated with tamoxifen) 16,279 European ancestry individuals NA NR [10000000] (imputed) 1 response to tamoxifen, survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0009391, http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029062 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (treated with aromatase inhibitor) 8,817 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, response to aromatase inhibitor, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://purl.obolibrary.org/obo/GO_0061477, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029063 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (treated with Cyclophosphamide Methotrexate Fluorouracil (CMF)-like chemotherapy regimen) 2,344 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, response to combination chemotherapy, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0007965, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029064 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (treated with taxane) 5,463 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, breast carcinoma, response to taxane http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0008580 GCST90029065 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 5-year breast cancer-specific survival (treated with anthracyclines) 10,393 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, breast carcinoma, response to anthracycline-based chemotherapy http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0005257 GCST90029066 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival 91,686 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029042 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (<40 years) 7,281 European ancestry individuals NA NR [10000000] (imputed) 0 survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029043 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (grade 3 tumor) 22,737 European ancestry individuals NA NR [10000000] (imputed) 2 survival time, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90029044 Genome-wide genotyping array 2021-10-22 34407845 Morra A 2021-08-18 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/34407845 Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment. 15-year breast cancer-specific survival (ER positive treated with endocrine therapy) 30,137 European ancestry individuals NA NR [10000000] (imputed) 1 survival time, estrogen-receptor positive breast cancer, breast carcinoma, response to endocrine therapy http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1000649, http://www.ebi.ac.uk/efo/EFO_0000305, http://www.ebi.ac.uk/efo/EFO_0007613 GCST90029045 Genome-wide genotyping array 2022-02-07 29758381 Marees AT 2018-04-25 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/29758381 Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use. Alcohol consumption 13,640 individuals 367 cases, 25,141 controls Illumina [247850] 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST012717 Exome genotyping array [Exome array] 2022-02-07 29758381 Marees AT 2018-04-25 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/29758381 Exploring the role of low-frequency and rare exonic variants in alcohol and tobacco use. ICD10 Z72.0: Tobacco use 7,432 individuals 1,927 cases, 25,141 controls Illumina [247850] 2 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST012716 Exome genotyping array [Exome array] 2021-10-12 34184762 Gao C 2021-06-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34184762 Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals. Alanine aminotransferase levels 388,865 European ancestry individuals NA Affymetrix, Illumina [11000000] (imputed) 300 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90025866 Genome-wide genotyping array 2021-10-12 34184762 Gao C 2021-06-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34184762 Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals. Aspartate aminotransferase levels 388,865 European ancestry individuals NA Affymetrix, Illumina [11000000] (imputed) 336 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90025867 Genome-wide genotyping array 2021-10-12 34184762 Gao C 2021-06-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34184762 Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals. Alanine aminotransferase levels x BMI interaction 388,865 European ancestry individuals NA Affymetrix, Illumina [11000000] (imputed) 9 serum alanine aminotransferase measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90025868 Genome-wide genotyping array 2021-10-12 34184762 Gao C 2021-06-29 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34184762 Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals. Aspartate aminotransferase levels x BMI interaction 388,865 European ancestry individuals NA Affymetrix, Illumina [11000000] (imputed) 12 aspartate aminotransferase measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004736, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90025869 Genome-wide genotyping array 2021-10-20 34309201 Yu Y 2021-07-26 Mol Oncol www.ncbi.nlm.nih.gov/pubmed/34309201 A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer. Disease free survival in colorectal cancer 505 European ancestry individuals NA Illumina [4711309] (imputed) 15 disease free survival http://www.ebi.ac.uk/efo/EFO_0000409 GCST90053837 Genome-wide genotyping array 2021-10-20 34309201 Yu Y 2021-07-26 Mol Oncol www.ncbi.nlm.nih.gov/pubmed/34309201 A comprehensive analysis of SNPs and CNVs identifies novel markers associated with disease outcomes in colorectal cancer. Recurrence-free survival in colorectal cancer 505 European ancestry individuals NA Illumina [4711309] (imputed) 0 event free survival time http://www.ebi.ac.uk/efo/EFO_0000482 GCST90053838 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been offered or sought treatment for anxiety (UKB data field 21062) 34,901 European ancestry cases, 119,860 European ancestry controls NA Affymetrix, Illumina [262175] 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90078826 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Kidney stone ureter stone bladder stone (Gene-based burden) 3,697 European ancestry cases, 328,057 European ancestry controls NA Illumina [184201] 0 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90081698 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever been offered or sought treatment for depression (UKB data field 21063) 37,813 European ancestry cases, 116,887 European ancestry controls NA Affymetrix, Illumina [262095] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078827 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20: kidney stone ureter stone bladder stone (Gene-based burden) 3,296 European ancestry cases, 325,756 European ancestry controls NA Illumina [184145] 0 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90081699 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 1 (UKB data field 21040) 25,542 European ancestry cases, 128,881 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078766 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Liver, biliary or pancreas problem (Gene-based burden) 796 European ancestry cases, 330,958 European ancestry controls NA Illumina [184201] 0 biliary tract disease, pancreas disease, liver disease http://www.ebi.ac.uk/efo/EFO_0009534, http://www.ebi.ac.uk/efo/EFO_0009605, http://www.ebi.ac.uk/efo/EFO_0001421 GCST90081675 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 2 (UKB data field 21040) 21,603 European ancestry cases, 132,820 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078767 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K87: Liver, biliary or pancreas problem (Gene-based burden) 753 European ancestry cases, 328,299 European ancestry controls NA Illumina [184145] 0 biliary tract disease, pancreas disease, liver disease http://www.ebi.ac.uk/efo/EFO_0009534, http://www.ebi.ac.uk/efo/EFO_0009605, http://www.ebi.ac.uk/efo/EFO_0001421 GCST90081676 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 3 (UKB data field 21040) 12,583 European ancestry cases, 141,840 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078768 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malabsorption coeliac disease (Gene-based burden) 1,968 European ancestry cases, 329,786 European ancestry controls NA Illumina [184201] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90081845 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 4 (UKB data field 21040) 7,543 European ancestry cases, 146,880 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078769 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K90: malabsorption coeliac disease (Gene-based burden) 1,766 European ancestry cases, 327,286 European ancestry controls NA Illumina [184145] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90081846 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 5 (UKB data field 21040) 18,335 European ancestry cases, 136,088 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078770 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malaria (Gene-based burden) 563 European ancestry cases, 331,191 European ancestry controls NA Illumina [184201] 0 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST90081834 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 6 (UKB data field 21040) 9,480 European ancestry cases, 144,943 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078771 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mania bipolar disorder manic depression (Gene-based burden) 1,240 European ancestry cases, 330,514 European ancestry controls NA Illumina [184201] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90081753 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 7 (UKB data field 21040) 11,287 European ancestry cases, 143,136 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078772 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F31: mania bipolar disorder manic depression (Gene-based burden) 1,129 European ancestry cases, 327,922 European ancestry controls NA Illumina [184145] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90081754 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 8 (UKB data field 21040) 8,837 European ancestry cases, 145,586 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078773 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Measles morbillivirus (Gene-based burden) 6,073 European ancestry cases, 325,681 European ancestry controls NA Illumina [184201] 0 measles http://www.ebi.ac.uk/efo/EFO_1002025 GCST90081927 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 9 (UKB data field 21040) 4,696 European ancestry cases, 149,727 European ancestry controls NA Affymetrix, Illumina [261686] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078774 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B05: measles morbillivirus (Gene-based burden) 5,294 European ancestry cases, 323,758 European ancestry controls NA Illumina [184145] 0 measles http://www.ebi.ac.uk/efo/EFO_1002025 GCST90081928 Exome-wide sequencing 2022-07-18 35577822 Liu PH 2022-05-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35577822 A genome-wide association study for melatonin secretion. Urine 6-hydroxymelatonin sulfate-to-creatinine ratio 2,373 Han Chinese ancestry individuals NA Affymetrix [7897704] (imputed) 5 urinary 6‑hydroxymelatonin sulfate to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0021488 GCST90101875 Genome-wide genotyping array 2020-10-30 33045005 Vogelezang S 2020-10-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33045005 Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits. Childhood body mass index 39,620 European ancestry individuals NA Affymetrix, Illumina [8227808] (imputed) 47 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90002409 Genome-wide genotyping array 2021-06-08 33219367 Li W 2020-11-20 Prostate Cancer Prostatic Dis www.ncbi.nlm.nih.gov/pubmed/33219367 Genome-wide association study identifies a role for the progesterone receptor in benign prostatic hyperplasia risk. Benign prostatic hyperplasia 1,942 cases, 4,730 controls 5,109 cases, 161,911 controls NR [5474821] (imputed) 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST011827 Genome-wide genotyping array 2020-11-12 33106285 Lopez-Isac E 2020-10-26 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33106285 Combined genetic analysis of juvenile idiopathic arthritis clinical subtypes identifies novel risk loci, target genes and key regulatory mechanisms. Arthritis (juvenile idiopathic) 3,305 European ancestry cases, 9,196 European ancestry controls 2,751 European ancestry cases, 15,886 European ancestry controls Illumina [7461261] (imputed) 17 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST90010715 Genome-wide genotyping array 2021-09-08 33817668 Curtis SW 2021-04-01 HGG Adv www.ncbi.nlm.nih.gov/pubmed/33817668 The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Bilateral cleft lip 15 Asian ancestry cases, 13 European ancestry cases, 15 Hispanic cases, 1 case, 161 Asian ancestry controls, 835 European ancestry controls, 626 Hispanic controls, 4 controls NA Illumina [539000] (imputed) 91 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST012352 Genome-wide genotyping array 2021-09-08 33817668 Curtis SW 2021-04-01 HGG Adv www.ncbi.nlm.nih.gov/pubmed/33817668 The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Unilateral cleft lip 184 Asian ancestry cases, 151 European ancestry cases, 167 Hispanic cases, 161 Asian ancestry controls, 835 European ancestry controls, 626 Hispanic controls, 4 controls NA Illumina [539000] (imputed) 23 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST012351 Genome-wide genotyping array 2021-09-08 33817668 Curtis SW 2021-04-01 HGG Adv www.ncbi.nlm.nih.gov/pubmed/33817668 The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Bilateral cleft lip and palate 121 Asian ancestry cases, 159 European ancestry cases, 285 Hispanic cases, 1 case, 161 Asian ancestry controls, 835 European ancestry controls, 626 Hispanic controls, 4 controls NA Illumina [539000] (imputed) 37 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST012350 Genome-wide genotyping array 2021-09-08 33817668 Curtis SW 2021-04-01 HGG Adv www.ncbi.nlm.nih.gov/pubmed/33817668 The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Unilateral cleft lip and palate 205 Asian ancestry cases, 315 European ancestry cases, 692 Hispanic cases, 1 case, 161 Asian ancestry controls, 835 European ancestry controls, 626 Hispanic controls, 4 controls NA Illumina [539000] (imputed) 43 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST012349 Genome-wide genotyping array 2021-09-08 33817668 Curtis SW 2021-04-01 HGG Adv www.ncbi.nlm.nih.gov/pubmed/33817668 The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Cleft lip (bilateral vs unilateral) 15 Asian ancestry bilateral cases, 13 European ancestry bilateral cases, 15 Hispanic bilateral cases, 1 bilateral case, 184 Asian ancestry unilateral cases, 151 European ancestry unilateral cases, 167 Hispanic unilateral cases, 161 Asian ancestry controls, 835 European ancestry controls, 626 Hispanic controls, 4 controls 28 bilateral cases, 329 unilateral cases Illumina [539000] (imputed) 0 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST012348 Genome-wide genotyping array 2021-09-08 33817668 Curtis SW 2021-04-01 HGG Adv www.ncbi.nlm.nih.gov/pubmed/33817668 The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Cleft palate (bilateral vs unilateral) 121 Asian ancestry bilateral cases, 159 European ancestry bilateral cases, 285 Hispanic bilateral cases, 1 bilateral case, 205 Asian ancestry unilateral cases, 315 European ancestry unilateral cases, 692 Hispanic unilateral cases, 1 unilateral case, 161 Asian ancestry controls, 835 European ancestry controls, 626 Hispanic controls, 4 controls 301 bilateral cases, 678 unilateral cases Illumina [539000] (imputed) 0 Cleft palate http://purl.obolibrary.org/obo/HP_0000175 GCST012347 Genome-wide genotyping array 2021-09-08 33817668 Curtis SW 2021-04-01 HGG Adv www.ncbi.nlm.nih.gov/pubmed/33817668 The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip. Cleft lip with or without cleft palate (bilateral vs unilateral) 15 Asian ancestry bilateral cleft lip cases, 184 Asian ancestry unilateral cleft lip cases, 121 Asian ancestry bilateral cleft palate cases, 205 Asian ancestry unilateral cleft palate cases, 13 European ancestry bilateral cleft lip cases, 151 European ancestry unilateral cleft lip cases, 159 European ancestry bilateral cleft palate cases, 315 European ancestry unilateral cleft palate cases, 15 Hispanic bilateral cleft lip cases,167 Hispanic unilateral cleft lip cases, 285 Hispanic bilateral cleft palate cases, 692 Hispanic unilateral cleft palate cases, 1 bilateral cleft lip case, 1 bilateral cleft palate case, 1 unilateral cleft palate case, 161 Asian ancestry controls, 835 European ancestry controls, 626 Hispanic controls, 4 controls NA Illumina [539000] (imputed) 3 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST012346 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAG1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088915 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAG1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089808 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAG2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088916 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAK2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 tyrosine-protein kinase JAK2 measurement http://www.ebi.ac.uk/efo/EFO_0020825 GCST90086866 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAK2 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase JAK2 measurement http://www.ebi.ac.uk/efo/EFO_0020825 GCST90088858 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAKMIP3 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090486 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CENPW 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090346 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEP57 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086654 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEP57 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090485 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEP57 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090900 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CER1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089309 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CERS5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087479 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CES1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089713 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CETN2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087361 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CETP 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 cholesteryl ester transfer protein measurement http://www.ebi.ac.uk/efo/EFO_0009133 GCST90089679 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CETP 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 cholesteryl ester transfer protein measurement http://www.ebi.ac.uk/efo/EFO_0009133 GCST90089680 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFAP45 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089493 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFB 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088587 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFC1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088296 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFD 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087603 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFD 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088142 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFH 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088615 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFHR1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089253 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFHR4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089450 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFHR5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088484 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC7A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088452 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLECL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087861 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLGN 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086359 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLIC1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088870 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLIC4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087022 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLIC5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087010 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLINT1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086842 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLK2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086687 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLMP 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086270 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLMP 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090767 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLN5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090354 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLN5 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090828 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLPB 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086389 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLPB 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086425 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLPB 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086877 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLPS 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089194 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLPSL1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090737 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLPSL2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089818 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLSTN3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089342 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLTC 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087627 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLU 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007655 GCST90088727 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CMA1 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088379 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CMPK1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088773 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CMPK1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090121 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNDP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089039 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIN 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 kin of IRRE-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020521 GCST90087465 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIN 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 kin of IRRE-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020521 GCST90087896 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR2DL2 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089822 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR2DL4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088918 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR2DL4 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090578 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR2DL5A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089840 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR2DL5A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089975 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR2DS2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086264 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR3DL2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088919 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR3DL3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089939 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR3DL3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090011 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIR3DS1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088920 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIRREL2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089950 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIRREL2 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090907 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIRREL3 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088739 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KISS1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089526 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIT 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087948 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KITLG 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090667 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLC1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087129 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLHL12 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087161 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLHL13 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087005 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLHL7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087107 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089429 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089306 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK11 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088091 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CISD1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089801 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CISD2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090047 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CKAP2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089008 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CKAP4 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089745 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CKB;CKM 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088494 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CKB;CKM 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088516 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CKLF 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089281 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CKM 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088012 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CKS1B 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087049 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLC 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086534 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLCA1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086303 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLCA2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090401 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLCF1;CRLF1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087976 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLCNKB 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087607 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC10A 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086513 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC11A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088152 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC11A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088721 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC12A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086597 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC12B 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086469 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC14A 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086283 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC1B 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088666 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAM2 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088175 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAM3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088176 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAML 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088917 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JAML 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090065 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KDELC1 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089528 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KDELC2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090109 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KDR 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088480 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KEAP1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087073 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KEAP1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090219 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KEL 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089643 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KERA 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086440 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA0040 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087880 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA0319 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086184 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA0319L 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087618 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1024 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090490 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1161 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090027 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1161 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090046 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1324 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086382 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1324 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090507 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1324L 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090155 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1549L 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086567 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA1644 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086266 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIAA2013 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089484 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIF16B 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086850 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIF1BP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087319 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIF1C 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090897 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIF22 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087193 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIF23 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 kinesin-like protein KIF23 measurement http://www.ebi.ac.uk/efo/EFO_0020522 GCST90088966 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KIF3A 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087684 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFHR5 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089901 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFI 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087960 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFL1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088626 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFP 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088149 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CFTR 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089789 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CGA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087747 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CGA;CGB3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088810 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CGA;FSHB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088193 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CGA;LHB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088147 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CGA;TSHB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088434 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CGB7 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089298 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CGREF1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089324 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHAD 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087455 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHCHD10 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086651 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHCHD2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089987 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHD7 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087710 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHEK1 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088106 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHEK2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088340 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHFR 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086684 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHGA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086594 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHGA 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090214 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHGB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090067 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHI3L1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086540 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHI3L2 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090672 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHIC2 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086498 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHIT1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086282 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHIT1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088450 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHKB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087385 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHKB 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089813 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHL1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088451 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHL1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090409 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHMP3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087033 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHP1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087000 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHRD 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087443 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHRDL1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088342 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHRDL2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089279 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089844 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST11 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089826 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST12 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089536 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST14 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089769 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST15 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087779 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST15 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088702 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088685 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089719 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089626 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST6 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088686 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CHST9 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086834 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CILP 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089165 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CILP2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090334 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CIRBP 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087186 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JARID2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087106 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JCHAIN 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090154 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JPH1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089584 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JPH3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090501 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JPH4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090515 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JTB 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090464 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein JUN 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086237 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KAT2B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086938 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KAT6A 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 histone acetyltransferase kat6a measurement http://www.ebi.ac.uk/efo/EFO_0020451 GCST90088113 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KAZALD1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089691 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNA10 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087347 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNAB2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086186 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNE2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086263 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNE3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090026 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNE5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090275 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNE5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090377 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNF1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087258 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNG4 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087505 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNIP1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087582 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNIP3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086316 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNIP4 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089619 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNJ11 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089993 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNMB3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090374 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCNN1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087513 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KCTD5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087009 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK11 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089823 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK12 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088264 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK13 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086572 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK13 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088265 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK14 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088486 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK14 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090240 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK15 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089457 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087619 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNDP1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089890 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNDP2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088258 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNEP1R1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087509 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNGA2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087282 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNOT1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087469 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNOT9 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090421 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNP 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089527 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTF 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088417 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTFR 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087783 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTFR 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088030 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTN1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088159 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTN2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088297 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTN4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088298 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTN5 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088299 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTNAP1 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087885 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTNAP2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089595 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CNTNAP5 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090468 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COA3 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089904 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COCH 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089749 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COG8 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090745 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL11A2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086656 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL13A1 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089502 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL15A1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090420 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL18A1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087926 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL1A1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086563 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COMMD7 5,314 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088086 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COMP 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090009 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK6 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088395 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK7 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088351 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK8 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087625 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK8 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088093 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK9 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089202 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLKB1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088608 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRB1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086455 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRC1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089105 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRC3 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086805 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRC3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089837 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRC4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086336 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRF1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088921 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRF1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089810 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRG1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086333 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRG2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086406 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRG2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086443 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRK1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087778 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLRK1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088212 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KMT2C 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086729 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KMT2D 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087568 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KMT5C 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086994 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KNG1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088717 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KNG1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088814 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCORL 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088657 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090797 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCT 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090451 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCTL 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086487 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LDHA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090808 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LDHB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088568 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LDHC 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090841 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LDLR 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087393 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LDLRAD4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090442 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LDOC1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090166 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LEAP2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089160 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LECT1 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090914 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LECT2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089250 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LEMD1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090006 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LEP 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087964 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LEP 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090217 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LEP 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090218 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COPS2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087726 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COPS7B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086947 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COQ8B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090827 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COTL1 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088801 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX4I2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089875 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX5B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089903 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX6A1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086306 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COX6A2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086329 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAG3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088922 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAG3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090928 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAIR1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086662 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAIR2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089678 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LALBA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089996 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAMA1;LAMB1;LAMC1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088035 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAMA4 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089508 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAMC2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090762 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAMP3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090650 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAMTOR3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087021 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LANCL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087700 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LANCL2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087110 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAP3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087682 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LARGE1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089936 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAT 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086335 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAT2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089093 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAYN 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087995 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LBP 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088224 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCK 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90088396 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCK 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90088741 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCMT1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088635 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCN1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086860 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCN10 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087335 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCN2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088095 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LCN8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089116 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KNG1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089829 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KPNA2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088111 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KPNA4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087164 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KPNA6 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087688 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KPNB1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088565 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRAS 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088956 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRBA2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086884 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KREMEN1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089470 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KREMEN2 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088267 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090917 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT17 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087307 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT18 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089016 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT20 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087326 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT23 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087843 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT5 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086590 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT7 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086721 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRT72 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086801 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRTAP2-4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087883 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KRTDAP 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089184 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KYAT3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087148 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KYNU 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088740 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein L1CAM 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088639 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein L3MBTL2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087174 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LACRT 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089704 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LAD1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089404 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL1A1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087470 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL20A1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090308 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL23A1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088728 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL25A1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089614 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL26A1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090743 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL28A1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086412 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL4A3BP 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087511 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL4A3BP 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087678 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL6A1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086571 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL6A2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089280 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL6A2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090494 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL6A3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086314 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL6A3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086602 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL6A5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086574 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL8A1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088775 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL9A1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089539 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COL9A2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090833 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COLEC10 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089497 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COLEC11 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088687 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COLEC12 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089040 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COLEC12 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090823 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COLGALT1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089114 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COLGALT2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089753 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COLQ 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090726 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein COMMD1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087034 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090209 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088092 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087735 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein KLK5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088266 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC2A 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086512 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC2B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089831 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC2D 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089634 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC2L 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090072 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC3B 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089156 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC4A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090341 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC4C 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090504 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC4D 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089806 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC4E 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089647 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC4G 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086447 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC4M 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088191 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC5A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090101 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CLEC6A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089561 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease x ever smoker interaction (2df) 21,077 European ancestry cases, 179,689 European ancestry controls NA Affymetrix [9886854] (imputed) 48 smoking status measurement, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016585 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease x ever smoker interaction (main effect) 21,077 European ancestry cases, 179,689 European ancestry controls NA Affymetrix [9886854] (imputed) 32 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016586 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease x ever smoker interaction (1df) 21,077 European ancestry cases, 179,689 European ancestry controls NA Affymetrix [9886854] (imputed) 1 smoking status measurement, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016587 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease in ever smokers 12,446 European ancestry cases, 59,145 European ancestry controls NA Affymetrix [9886854] (imputed) 33 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016588 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease in never smokers 8,631 European ancestry cases, 120,544 European ancestry controls NA Affymetrix [9886854] (imputed) 32 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016589 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease x current smoker interaction (2df) 21,077 European ancestry cases, 179,689 European ancestry controls NA Affymetrix [9886854] (imputed) 55 smoking status measurement, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016590 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease x current smoker interaction (main effect) 21,077 European ancestry cases, 179,689 European ancestry controls NA Affymetrix [9886854] (imputed) 54 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016591 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease x current smoker interaction (1df) 21,077 European ancestry cases, 179,689 European ancestry controls NA Affymetrix [9886854] (imputed) 1 smoking status measurement, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016592 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease in current smokers 4,589 European ancestry cases, 10,001 European ancestry controls NA Affymetrix [9886854] (imputed) 7 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016593 Genome-wide genotyping array 2021-04-23 33106845 Kim W 2020-10-27 Am J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33106845 Genome-wide Gene-by-smoking Interaction Study of Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease in non-current smokers 16,488 European ancestry cases, 169,688 European ancestry controls NA Affymetrix [9886854] (imputed) 54 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90016594 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z37.0: Single live birth (Gene-based burden) 11,980 European ancestry cases, 199,928 European ancestry controls NA Illumina [179939] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90085235 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - folic acid product 3,838 European ancestry cases, 316,920 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078055 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z37.9: Outcome of delivery, unspecified (Gene-based burden) 863 European ancestry cases, 386,006 European ancestry controls NA Illumina [185331] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90085236 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - food supplement plant herbal extract 1,616 European ancestry cases, 319,142 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078238 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z39: Encounter for maternal postpartum care and examination (Gene-based burden) 1,977 European ancestry cases, 208,474 European ancestry controls NA Illumina [179794] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085238 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fosamax 532 European ancestry cases, 320,226 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078208 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z40: Encounter for prophylactic surgery (Gene-based burden) 40,136 European ancestry cases, 307,162 European ancestry controls NA Illumina [184593] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085240 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - frusemide 776 European ancestry cases, 319,982 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078036 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z40.0: Encounter for prophylactic surgery for risk factors related to malignant neoplasms (Gene-based burden) 796 European ancestry cases, 387,134 European ancestry controls NA Illumina [19298] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085239 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - furosemide 3,399 European ancestry cases, 317,359 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078136 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z41: Encounter for procedures for purposes other than remedying health state (Gene-based burden) 914 European ancestry cases, 386,561 European ancestry controls NA Illumina [185342] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085242 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fybogel mebeverine sachet 665 European ancestry cases, 320,093 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078028 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z41.1: Encounter for cosmetic surgery (Gene-based burden) 852 European ancestry cases, 386,781 European ancestry controls NA Illumina [185342] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085241 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cystitis (Gene-based burden) 661 European ancestry cases, 331,093 European ancestry controls NA Illumina [184201] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90081900 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50.1: Vascular disorders of male genital organs 688 European ancestry cases, 175,465 European ancestry controls NA Affymetrix, Illumina [288783] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90080632 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30: Cystitis (Gene-based burden) 546 European ancestry cases, 328,506 European ancestry controls NA Illumina [184145] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90081901 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N42.8: Other specified disorders of prostate 736 European ancestry cases, 175,360 European ancestry controls NA Affymetrix, Illumina [288715] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90080621 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Deep venous thrombosis (Gene-based burden) 8,947 European ancestry cases, 322,807 European ancestry controls NA Illumina [184201] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90081655 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever highly irritable - argumentative for 2 days (UKB data field 4653) 30,880 European ancestry cases, 143,261 European ancestry controls NA Affymetrix, Illumina [288657] 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90079215 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I80: deep venous thrombosis (Gene-based burden) 8,088 European ancestry cases, 320,964 European ancestry controls NA Illumina [184145] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90081656 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N42: Other and unspecified disorders of prostate 1,670 European ancestry cases, 174,103 European ancestry controls NA Affymetrix, Illumina [288299] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90080622 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression (Gene-based burden) 27,241 European ancestry cases, 304,513 European ancestry controls NA Illumina [184201] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90081747 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N47: Disorders of prepuce 2,528 European ancestry cases, 173,085 European ancestry controls NA Affymetrix, Illumina [288070] 0 phimosis http://www.ebi.ac.uk/efo/EFO_1001104 GCST90080627 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F32: depression (Gene-based burden) 23,026 European ancestry cases, 306,026 European ancestry controls NA Illumina [184145] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90081748 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever manic hyper for 2 days (UKB data field 4642) 9,621 European ancestry cases, 164,125 European ancestry controls NA Affymetrix, Illumina [287952] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079214 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-05-10 33190678 Ho YYW 2020-10-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/33190678 Comparison of Genome-Wide Association Scans for Quantitative and Observational Measures of Human Hair Curvature. Hair curvature (quantitative) 2,225 European ancestry individuals NA Illumina [7533529] (imputed) 33 hair morphology measurement http://www.ebi.ac.uk/efo/EFO_0007821 GCST011641 Genome-wide genotyping array 2021-05-10 33190678 Ho YYW 2020-10-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/33190678 Comparison of Genome-Wide Association Scans for Quantitative and Observational Measures of Human Hair Curvature. Hair curvature (observational) 2,225 European ancestry individuals NA Illumina [7533529] (imputed) 3 hair morphology measurement http://www.ebi.ac.uk/efo/EFO_0007821 GCST011640 Genome-wide genotyping array 2021-09-28 33985508 Williams CJ 2021-05-13 J Biomed Sci www.ncbi.nlm.nih.gov/pubmed/33985508 Genome wide association study of response to interval and continuous exercise training: the Predict-HIIT study. Peak oxygen uptake response following exercise training 507 European ancestry individuals 39 European ancestry individuals Illumina [NR] (imputed) 0 maximal oxygen uptake measurement, response to exercise http://www.ebi.ac.uk/efo/EFO_0004887, http://www.ebi.ac.uk/efo/EFO_0007768 GCST012405 Genome-wide genotyping array 2021-06-08 33941792 Yoshimura K 2021-05-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33941792 A web-based survey on various symptoms of computer vision syndrome and the genetic understanding based on a multi-trait genome-wide association study. Computer vision syndrome 1,966 Japanese ancestry individuals NA Illumina [540916] (imputed) 10 vision disorder http://purl.obolibrary.org/obo/MONDO_0021084 GCST011826 Genome-wide genotyping array 2021-03-01 33096046 Johnson EC 2020-10-20 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/33096046 A large-scale genome-wide association study meta-analysis of cannabis use disorder. Cannabis use disorder 17,068 European ancestry cases, 357,219 European ancestry controls, 3,848 African ancestry cases, 5,897 African ancestry controls NA Illumina [NR] (imputed) 4 cannabis dependence http://www.ebi.ac.uk/efo/EFO_0007191 GCST011179 Genome-wide genotyping array 2021-06-08 33958783 Liu G 2021-05-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33958783 Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease. Parkinson's disease progression (cognitive) 2,650 European and unknown ancestry individuals 1,171 individuals Illumina [11220132] (imputed) 10 disease progression measurement http://www.ebi.ac.uk/efo/EFO_0008336 GCST011823 Genome-wide genotyping array 2021-09-09 33907183 Guo S 2021-04-27 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33907183 Genome wide association study identifies four loci for early onset schizophrenia. Early-onset schizophrenia 1,256 Han Chinese ancestry cases, 2,661 Han Chinese ancestry controls 903 Han Chinese ancestry cases, 3,900 Han Chinese ancestry controls Illumina [4867007] (imputed) 15 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST012368 Genome-wide genotyping array 2021-09-07 33861876 Dao C 2021-04-16 Addiction www.ncbi.nlm.nih.gov/pubmed/33861876 The Impact of Removing Former Drinkers from Genome-wide Association Studies of AUDIT-C. Alcohol use disorder (consumption score) 5,135 European ancestry individuals inluding former drinkers, 126,375 European ancestry individuals excluding former drinkers NR NR [7682250] (imputed) 12 alcohol use disorder measurement, longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0009458, http://www.ebi.ac.uk/efo/EFO_0007645 GCST012336 Genome-wide genotyping array 2021-09-27 33830181 Tideman JWL 2021-04-08 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/33830181 Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia. Low myopia 11,197 European ancestry low myopic cases, 21,416 European ancestry emmetropia controls NA NR [13958389] (imputed) 66 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST012402 Genome-wide genotyping array 2021-09-27 33830181 Tideman JWL 2021-04-08 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/33830181 Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia. Hyperopia 10,828 European ancestry hyperopia cases, 21,416 European ancestry emmetropia controls NA NR [13958389] (imputed) 78 Hypermetropia http://purl.obolibrary.org/obo/HP_0000540 GCST012401 Genome-wide genotyping array 2021-09-27 33830181 Tideman JWL 2021-04-08 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/33830181 Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia. Low myopia vs hyperopia 11,197 European ancestry low myopia cases, 10,828 European ancestry hyperopia cases NA NR [13958389] (imputed) 145 Hypermetropia, Myopia http://purl.obolibrary.org/obo/HP_0000540, http://purl.obolibrary.org/obo/HP_0000545 GCST012400 Genome-wide genotyping array 2021-09-27 33830181 Tideman JWL 2021-04-08 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/33830181 Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia. High myopia 3,164 European ancestry high myopic cases, 21,416 European ancestry emmetropia controls NA NR [13958389] (imputed) 152 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST012403 Genome-wide genotyping array 2022-05-31 35530816 Taub MA 2022-01-13 Cell Genom www.ncbi.nlm.nih.gov/pubmed/35530816 Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Telomere length 51,654 European ancestry individuals, 29,260 African ancestry individuals, 18,091 Hispanic or Latin American individuals, 5,683 Asian ancestry individuals, 4,503 individuals NA NR [163000000] 93 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90103979 Genome-wide sequencing 2021-05-12 31577861 Dai J 2019-10-31 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31577861 Genome-wide association study of INDELs identified four novel susceptibility loci associated with lung cancer risk. Lung cancer 20,871 European ancestry cases, 15,971 European ancestry controls, 2,331 Chinese ancestry cases, 3,077 Chinese ancestry controls NA Illumina [484196] 19 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST011656 Targeted genotyping array [Oncoarray] 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPTN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089724 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPTX1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090587 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPTX2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089474 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPTXR 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090436 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPW 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090948 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NQO1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090849 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NQO2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090801 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR1D1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088970 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR1D2 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087291 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR1H2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090450 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR1H4 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090397 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR3C1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088108 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR3C2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087310 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR4A1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090043 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NR5A2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086987 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRAS 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086326 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRBP1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087099 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRCAM 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 neuronal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020602 GCST90088931 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRG1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090537 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRG2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090020 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRG3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086527 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRG4 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087813 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRN1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090309 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088275 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRP1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089072 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NNMT 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087548 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOG 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 8 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089221 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOG 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 10 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090292 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOTCH1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 neurogenic locus notch homolog protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008246 GCST90088929 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOTCH2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90086671 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOTCH2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90088928 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOTCH2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90090191 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOTCH3 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 neurogenic locus notch homolog protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020600 GCST90088930 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOTUM 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090080 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOV 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 protein nov homolog measurement http://www.ebi.ac.uk/efo/EFO_0020685 GCST90088040 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NOVA1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087067 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPC2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089325 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPDC1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086260 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPFF 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089096 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPHS2 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090741 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPIPB3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090931 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPLOC4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087334 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPM1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090351 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPNT 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089355 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPPA 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089036 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPPB 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086250 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPPB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088496 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPPB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089781 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPPC 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090513 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NPS 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089391 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RFK 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087354 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RFNG 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089734 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RFXAP 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087187 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGMA 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089056 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGMB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088321 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGS10 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086829 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGS18 5,321 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087696 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGS19 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087178 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGS3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087254 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGS7 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087057 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RGS8 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086845 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RHOA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090866 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RHOD 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086986 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RHOG 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087058 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RHPN2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086746 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RIC3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086624 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RIC3 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089675 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RIDA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087895 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RIPK2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090417 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RIPK2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090434 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RIPPLY1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090812 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RLBP1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087313 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RLN1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089347 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RLN2 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089532 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RLN3 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089261 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBP7 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087836 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RCAN1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087458 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RCN1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090630 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RCN2 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086387 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RCVRN 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087870 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RDH16 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087289 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RECQL 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086741 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REG1A 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087370 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REG1B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089151 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REG3A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090601 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REG3G 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090648 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REG4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086538 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RELB 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086760 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RELL1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087420 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RELL2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089521 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RELT 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087794 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RELT 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088936 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REN 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088361 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REPIN1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087524 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RET 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088279 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RETN 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088205 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RETSAT 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090169 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein REXO2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087546 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RFESD 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087555 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RFFL 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087829 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RMDN1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089657 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RMDN3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090610 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RMI1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087660 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089740 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE10 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089085 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE13 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089419 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RNASE2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090180 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NISCH 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087196 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLGN1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090015 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLGN2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090458 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLGN2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090815 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLGN3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090393 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLGN4X 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089019 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLRP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086843 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLRP10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087250 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NLRP4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087231 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NMB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90090629 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NME1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089236 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NME2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088640 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NMRAL1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087701 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NMS 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090722 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NMT1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086990 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NMT1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088957 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NMU 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090273 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NNAT 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090666 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRP2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089516 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRSN1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086839 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRXN1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088932 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRXN1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090418 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRXN2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090355 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRXN3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088933 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRXN3 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089656 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NRXN3 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090830 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NSDHL 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090004 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NSF 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087704 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NSFL1C 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088641 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NSG1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089843 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NT5C 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087069 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NT5C2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086666 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NT5DC3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090525 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NT5E 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089608 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTF3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088602 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTF4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088603 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTM 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086495 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTM 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090196 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTMT1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086996 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTN1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089541 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F7 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088253 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F8 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087484 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F9 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088790 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F9 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088997 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAAH2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090181 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FABP1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086776 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FABP3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088756 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FABP4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090863 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FABP5 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088845 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FABP6 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089433 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAF2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089590 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAF2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090279 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAF2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090790 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAH 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086736 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAIM 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086258 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM107A 5,318 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 protein fam107a measurement http://www.ebi.ac.uk/efo/EFO_0020673 GCST90088054 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM107B 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 protein fam107b measurement http://www.ebi.ac.uk/efo/EFO_0020674 GCST90088770 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM107B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 protein fam107b measurement http://www.ebi.ac.uk/efo/EFO_0020674 GCST90089842 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM134B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090228 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM150B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089338 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM151A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089880 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM159A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087438 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM159B 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086309 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM159B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086380 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM162A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089481 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM162B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086581 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM163A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089326 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FAM163B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086482 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAP1GAP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087648 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAP1GDS1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087788 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAP2A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090886 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAPGEF5 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090479 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RARRES1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090183 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RARRES2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088227 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RARRES3 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086516 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RASA1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089054 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RB1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088880 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBBP5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087573 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBBP6 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090888 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBBP9 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086213 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBFOX2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086759 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBL1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087287 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBL2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087529 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM19 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086762 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM22 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087328 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM23 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086811 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM24 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086718 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM28 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086888 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087201 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM39 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088652 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBM46 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087681 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBP4 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089055 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RBP4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089863 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INSL6 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089198 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INSR 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088393 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INSRR 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089358 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INTS3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086889 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IQCF1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089968 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IQCF3 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087444 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IRF1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086180 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IRF1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086235 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IRF2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087237 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IRF4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090868 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IRF6 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090956 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IRF9 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086985 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISCU 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089732 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISG15 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087818 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISG15 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087821 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086792 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISLR2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087390 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISLR2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090224 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISM1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090148 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISM2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089334 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ISOC1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090837 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IST1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086981 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITCH 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087063 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITFG1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090645 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGA1;ITGB1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088423 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH15 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089030 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088513 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH3 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088001 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088084 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH6 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088446 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH7 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089951 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDHR1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090162 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDHR3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090060 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDHR3 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090703 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDHR5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090937 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDK2;CCNA2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088337 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDK2AP1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090696 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDK5;CDK5R1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088338 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDK8;CCNC 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088339 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDKN1B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088495 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDKN2B 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090878 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDKN2C 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087043 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDKN2D 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086943 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDKN3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087828 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDNF 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087615 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDNF 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088828 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDON 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088726 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDSN 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089652 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDY1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089658 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDYL2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086436 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD86 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089311 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD8A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089255 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD8B 5,327 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090621 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD93 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086604 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD93 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087812 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD96 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090751 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD96 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090789 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD99L2 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086330 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDC25A 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086791 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDC25B 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086975 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDC34 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087051 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDC37 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 hsp90 co-chaperone CDC37 measurement http://www.ebi.ac.uk/efo/EFO_0020458 GCST90088563 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDC42 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090852 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDC42BPA 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087172 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDC42BPB 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088468 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDCP1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089500 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDCP1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090233 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087922 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087951 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH11 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089815 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH11 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090775 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH12 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086411 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH12 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088482 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH12 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090133 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CDH15 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086615 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGA2B;ITGB3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088503 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGA2B;ITGB3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090221 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGA5 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089577 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGAL 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086824 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGAV;ITGB5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088813 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGB2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087203 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGB5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089809 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGB6 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089794 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITGB7 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086609 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITIH1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089947 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITIH2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090631 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITIH3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089692 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITIH4 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088776 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITIH5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090066 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITM2A 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086318 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITM2A 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089816 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITM2A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090323 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITM2B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090040 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITM2C 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086341 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITM2C 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086492 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITM2C 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090734 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITPKA 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087462 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITPKC 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087032 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITPRIPL1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090562 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ITSN1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087758 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL7R 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088912 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL9 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008192 GCST90089218 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL9 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008192 GCST90090167 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ILF2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087137 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ILF3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087209 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ILK 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086208 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IMPA2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087084 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IMPAD1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090568 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IMPDH1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088967 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IMPDH2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088979 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086744 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ING1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088566 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INHBA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087649 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INHBA;INHBB 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088047 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INHBA;INHBB 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088673 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INHBA;INHBB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090208 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INHBB 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087602 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INHBC 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089405 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INPP5B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087118 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INPP5E 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086712 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INS 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088793 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INSIG1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086394 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INSL3 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089169 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INSL4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089407 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein INSL5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086284 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEL 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090829 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CELA1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089284 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CELA2A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089687 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CELA3B 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089362 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CELF2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089760 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEND1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089871 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CENPV 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090317 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL5RA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 interleukin 5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008186 GCST90087608 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL5RA 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 interleukin 5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008186 GCST90088714 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL6 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-6 receptor measurement http://www.ebi.ac.uk/efo/EFO_0004814 GCST90087963 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL6 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-6 receptor measurement http://www.ebi.ac.uk/efo/EFO_0004814 GCST90088753 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL6R 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-6 receptor measurement http://www.ebi.ac.uk/efo/EFO_0004814 GCST90088597 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL6R 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-6 receptor measurement http://www.ebi.ac.uk/efo/EFO_0004814 GCST90090045 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL6ST 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087986 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL7 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin 7 measurement http://www.ebi.ac.uk/efo/EFO_0008189 GCST90087742 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL7 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin 7 measurement http://www.ebi.ac.uk/efo/EFO_0008189 GCST90088598 Genome-wide genotyping array 2021-08-27 33816493 Cai R 2021-03-18 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33816493 Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome. SAPHO syndrome 49 Chinese ancestry cases, 121 Chinese ancestry controls NA Illumina [802276] 24 SAPHO syndrome http://www.ebi.ac.uk/efo/EFO_1001164 GCST012256 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEACAM1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089997 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEACAM19 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089631 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEACAM20 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086278 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEACAM21 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089735 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEACAM3 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090438 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEACAM4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086497 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEACAM7 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089715 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CEBPB 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086230 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CECR1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089276 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GMFG 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087355 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNAI3 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087124 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNAS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089201 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNGT2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086500 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNLY 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087784 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNLY 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088260 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNMT 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087711 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNPDA1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090378 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNPNAT1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087679 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNPTG 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086396 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNRH1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089103 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNRH2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086416 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNS 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088460 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GNS 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090122 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GOLM1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090304 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GOLM1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090427 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GORAB 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089762 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GOSR1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089845 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GOSR2 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086262 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GOT1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088808 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GP1BA 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088850 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GP5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089716 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GP6 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088259 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPA33 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089415 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPC1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090265 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSKIP 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087268 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLIN3 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087906 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLK1 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088360 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLOD2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089571 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLOD3 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086366 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLPP4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087520 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLS1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087195 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLSCR3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086732 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLTP 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089328 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLVAP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090229 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLXDC1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090572 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLXDC2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086351 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLXDC2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086694 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLXNA1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090443 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLXNB2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086476 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLXNB2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090558 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLXNC1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088745 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PMEL 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089451 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PMEPA1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089581 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PMS2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086679 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PMVK 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086992 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PNKP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087588 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PNLIPRP1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089537 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PNLIPRP2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089591 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PNP 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086197 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPR68 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087030 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPT 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088492 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPX5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090709 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GPX7 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090141 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRAMD1C 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090136 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRAMD1C 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090335 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRAP 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90087249 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRAP2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90088990 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRB10 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086704 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRB14 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087571 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRB2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90089045 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRB7 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086659 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GREM1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088692 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GREM2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089082 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRIA4 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086441 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRID1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087478 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRID2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087208 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRK2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088331 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRN 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088852 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRP 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089233 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRP 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090138 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRP 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090185 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GRPEL1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089666 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSK3A;GSK3B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088285 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSK3A;GSK3B 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088388 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein POU2F1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086863 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPA1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088878 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPARA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087318 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPARGC1A 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086868 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPBP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088073 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPBP 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088131 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPBP 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088729 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPCDC 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087707 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPFIA1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087691 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIA 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088542 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088976 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIB 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088764 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPID 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088959 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIE 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088971 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIF 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088977 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIF 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090048 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIH 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086991 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090885 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPIL2 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087863 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPM1A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087102 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPM1D 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086681 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPM1L 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089718 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP1R14B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090369 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP1R3B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087215 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PPP1R8 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087345 Genome-wide genotyping array 2021-04-22 31251335 Turpin W 2019-10-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/31251335 Analysis of Genetic Association of Intestinal Permeability in Healthy First-degree Relatives of Patients with Crohn's Disease. Intestinal permeability measurement 1,075 European ancestry first-degree relatives of Crohn’s disease patients NA Illumina [3700000] (imputed) 16 intestinal permeability measurement http://www.ebi.ac.uk/efo/EFO_0011031 GCST011536 Exome genotyping array [Exome array] 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UST 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090156 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UTS2 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089258 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UTS2B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089341 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UTS2R 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087508 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein UXS1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090085 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAMP3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089913 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAMP4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089791 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAMP5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090107 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAMP8 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089639 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAPA 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089705 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAPB 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089712 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VARS 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087363 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VASN 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089144 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VASP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090809 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAV1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088994 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VAV3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090843 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VCAM1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 vascular cell adhesion molecule-1 measurement http://www.ebi.ac.uk/efo/EFO_0010057 GCST90088153 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VCAN 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090752 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VCL 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090271 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VCY 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089344 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VDR 5,322 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086189 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VEGFA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90087729 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VEGFA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90087970 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VEGFA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90088788 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VEGFB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090698 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VTN 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090100 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VWA1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089386 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VWA2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089677 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VWC2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086551 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VWC2L 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089972 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VWF 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90088207 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WARS 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090875 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WBP1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086508 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WBP1L 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090740 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WDR1 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086424 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090626 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC10A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087436 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC10B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086407 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC11 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089958 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC12 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089264 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC13 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090644 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086723 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089385 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089598 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC6 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087428 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFDC8 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089695 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFIKKN1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088257 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFIKKN2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087425 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WFIKKN2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088284 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WIF1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088103 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VEGFC 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 vascular endothelial growth factor C measurement http://www.ebi.ac.uk/efo/EFO_0020848 GCST90088234 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VEGFD 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90087372 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VEGFD 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90087913 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VIMP 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086664 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VIP 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088435 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VIT 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089312 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VIT 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090780 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VNN2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089620 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VOPP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087886 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VPS29 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087864 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VPS4A 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086763 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VPS4B 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087139 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VRK1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087064 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSIG1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086879 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSIG1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090158 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSIG10 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086463 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSIG2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089990 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSNL1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087503 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSTM2L 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089490 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSTM4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089757 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VSTM5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090095 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VTA1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088627 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VTI1A 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089945 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VTI1B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090413 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein VTN 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087391 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WISP1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087614 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WISP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088213 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WISP2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089393 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WISP3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089240 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WNK3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089064 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WNT10A 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086202 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WNT11 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089534 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WNT3A 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087402 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WNT5A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087406 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WNT7A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088795 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WRNIP1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087047 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WSCD2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089332 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein WWP1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086675 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XCL1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087764 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XCL1 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088600 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XDH 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086647 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XG 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086300 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XG 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090010 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XPNPEP1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088411 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XRCC1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087054 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XRCC4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090887 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XRCC6 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088094 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein XXYLT1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089378 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YBX1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090799 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YBX2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089375 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YES1 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088121 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YIPF6 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090947 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YME1L1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086598 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YTHDC1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090357 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAB 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086966 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087823 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAE 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087824 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAE 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090174 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAG 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090372 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAQ 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089776 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAQ;SFN;YWHAB;YWHAE;YWHAG;YWHAH;YWHAZ 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088620 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAQ;SFN;YWHAB;YWHAE;YWHAG;YWHAH;YWHAZ 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088760 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein YWHAZ 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089224 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZAP70 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088540 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZAP70 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088706 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZAP70 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088707 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZBTB33 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087225 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZDHHC14 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086851 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZFP91 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087583 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZFYVE27 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087439 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZFYVE27 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090510 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZG16 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090057 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZG16B 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090120 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZHX1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087204 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZHX3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086195 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF10 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086802 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF134 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087227 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF174 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086766 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF175 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087181 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF18 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086714 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF180 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087216 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF23 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086800 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF264 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090952 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF275 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090778 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF276 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087909 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF329 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087238 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF334 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087212 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF358 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086324 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF382 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087884 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF41 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086177 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF410 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087262 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF415 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087242 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF526 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087887 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF560 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087059 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF566 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087232 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF75D 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086815 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF774 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087210 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNF843 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090127 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNRF3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086251 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNRF3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087435 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNRF3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087800 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZNRF4 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090705 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZP4 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089817 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZPBP 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090245 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZPBP2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086417 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZPLD1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089078 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ZYX 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087574 Genome-wide genotyping array 2021-11-04 30175238 Jackson VE 2018-01-12 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/30175238 Meta-analysis of exome array data identifies six novel genetic loci for lung function. Lung function (FVC) 60,749 European ancestry individuals, 7,721 African ancestry individuals 111,556 European ancestry individuals Illumina [179215] 6 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST012496 Exome genotyping array [Exome array] 2021-11-04 30175238 Jackson VE 2018-01-12 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/30175238 Meta-analysis of exome array data identifies six novel genetic loci for lung function. Lung function (FEV1/FVC) 60,749 European ancestry individuals, 7,721 African ancestry individuals 111,556 European ancestry individuals Illumina [179215] 5 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST012495 Exome genotyping array [Exome array] 2021-11-04 30175238 Jackson VE 2018-01-12 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/30175238 Meta-analysis of exome array data identifies six novel genetic loci for lung function. Lung function (FEV1) 60,749 European ancestry individuals, 7,721 African ancestry individuals 111,556 European ancestry individuals Illumina [179215] 4 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST012497 Exome genotyping array [Exome array] 2021-04-23 33830302 Inshaw JRJ 2021-04-08 Diabetologia www.ncbi.nlm.nih.gov/pubmed/33830302 Analysis of overlapping genetic association in type 1 and type 2 diabetes. Type 1 diabetes 7,467 European ancestry cases, 10,218 European ancestry controls NA Affymetrix, Illumina [7769284] (imputed) 8 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90000529 Genome-wide genotyping array 2021-04-23 33830302 Inshaw JRJ 2021-04-08 Diabetologia www.ncbi.nlm.nih.gov/pubmed/33830302 Analysis of overlapping genetic association in type 1 and type 2 diabetes. Type 1 or type 2 diabetes (pleiotropy) 81,591 European ancestry cases, 834,224 European ancestry controls NA Affymetrix, Illumina [at least 7769284] (imputed) 0 type 1 diabetes mellitus, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147, http://purl.obolibrary.org/obo/MONDO_0005148 GCST011539 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel broadband ultrasound attenuation left (UKB data field 4101) 166,276 European ancestry individuals NA Affymetrix, Illumina [278770] 1 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90079149 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture upper arm humerus elbow (Gene-based burden) 1,286 European ancestry cases, 330,468 European ancestry controls NA Illumina [184201] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90081954 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density right (UKB data field 4124) 166,266 European ancestry individuals NA Affymetrix, Illumina [278720] 1 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90079158 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42: fracture upper arm humerus elbow (Gene-based burden) 1,059 European ancestry cases, 327,993 European ancestry controls NA Illumina [184145] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90081955 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density left (UKB data field 4105) 166,186 European ancestry individuals NA Affymetrix, Illumina [278646] 1 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90079152 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture wrist colles fracture (Gene-based burden) 1,658 European ancestry cases, 330,096 European ancestry controls NA Illumina [184201] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90081958 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at first live birth (UKB data field 2754) 158,740 European ancestry individuals NA Affymetrix, Illumina [266608] 0 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST90078957 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62: fracture wrist colles fracture (Gene-based burden) 1,406 European ancestry cases, 327,646 European ancestry controls NA Illumina [184145] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90081959 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at last live birth (UKB data field 2764) 158,514 European ancestry individuals NA Affymetrix, Illumina [266266] 0 age at last pregnancy measurement http://www.ebi.ac.uk/efo/EFO_0009440 GCST90078958 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K25: gastric stomach ulcers (Gene-based burden) 3,114 European ancestry cases, 325,938 European ancestry controls NA Illumina [184145] 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90081682 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 5 (UKB data field 4968) 8,230 European ancestry cases, 148,723 European ancestry controls NA Affymetrix, Illumina [265421] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079239 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gastritis gastric erosions (Gene-based burden) 836 European ancestry cases, 330,918 European ancestry controls NA Illumina [184201] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90081683 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 6 (UKB data field 4968) 146,554 European ancestry cases, 10,399 European ancestry controls NA Affymetrix, Illumina [265421] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079240 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29: gastritis gastric erosions (Gene-based burden) 788 European ancestry cases, 328,264 European ancestry controls NA Illumina [184145] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90081684 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 7 (UKB data field 4968) 1,224 European ancestry cases, 155,729 European ancestry controls NA Affymetrix, Illumina [265421] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079241 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gastro oesophageal reflux or gastric reflux (Gene-based burden) 21,143 European ancestry cases, 310,611 European ancestry controls NA Illumina [184201] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90081678 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 8 (UKB data field 4968) 2,396 European ancestry cases, 154,557 European ancestry controls NA Affymetrix, Illumina [265421] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079242 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21: Gastro oesophageal reflux or gastric reflux (Gene-based burden) 18,674 European ancestry cases, 310,377 European ancestry controls NA Illumina [184145] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90081679 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by headaches in the last three months - 600 Not bothered at all (UKB data field 21051) 95,095 European ancestry cases, 60,063 European ancestry controls NA Affymetrix, Illumina [262697] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078794 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gestational hypertension pre eclampsia (Gene-based burden) 1,789 European ancestry cases, 329,965 European ancestry controls NA Illumina [184195] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90081639 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by headaches in the last three months - 601 Bothered a little (UKB data field 21051) 52,979 European ancestry cases, 102,179 European ancestry controls NA Affymetrix, Illumina [262697] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078795 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O13: gestational hypertension pre eclampsia (Gene-based burden) 1,593 European ancestry cases, 176,301 European ancestry controls NA Illumina [177166] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90081640 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by headaches in the last three months - 602 Bothered a lot (UKB data field 21051) 7,084 European ancestry cases, 148,074 European ancestry controls NA Affymetrix, Illumina [262697] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078796 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glaucoma (Gene-based burden) 5,059 European ancestry cases, 326,695 European ancestry controls NA Illumina [184201] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90081740 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by back pain in the past three months - 600 Not bothered at all (UKB data field 21048) 60,787 European ancestry cases, 94,352 European ancestry controls NA Affymetrix, Illumina [262673] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078785 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-10-04 33976257 Yusuf I 2021-05-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33976257 Genetic risk factors for colorectal cancer in multiethnic Indonesians. Colorectal cancer 89 Indonesian cases, 84 Indonesian controls NA Affymetrix [524765] (imputed) 3 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012421 Genome-wide genotyping array 2021-10-01 33948810 Gurinovich A 2021-05-04 Geroscience www.ncbi.nlm.nih.gov/pubmed/33948810 Effect of longevity genetic variants on the molecular aging rate. Longevity (100 years and older) 1,320 European ancestry cases, 2,899 European ancestry controls 312 Ashkenazi Jewish ancestry cases, 638 Ashkenazi Jewish ancestry controls Illumina [9039731] (imputed) 8 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST012419 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSPA1L 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086911 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSPA6 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087600 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSPA8 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089235 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSPA9 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087477 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSPB1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086539 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSPD1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088015 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTATIP2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086378 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTATIP2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089807 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTN1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086364 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTN3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086360 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTR2A 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087525 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTR6 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087527 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTR7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087519 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HTRA2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 serine protease HTRA2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020723 GCST90088311 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HYAL1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090119 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IAPP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089119 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IARS 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087246 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IBSP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087721 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IBSP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088372 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST90088669 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90087920 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90089058 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM3 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 intercellular adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020482 GCST90088005 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089491 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090702 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB14 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087855 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB17 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086549 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB18 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087317 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB22A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086963 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB26 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089610 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB27A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090723 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB27B 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087551 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB31 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087552 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB35 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087497 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB39B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086961 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB3D 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086446 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB5C 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087858 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB6B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087852 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAB7B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086964 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RABEPK 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087553 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAC1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088116 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAC3 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088992 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RACGAP1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087543 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAD1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087141 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAD23A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086211 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAD23B 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087044 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAD51 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 DNA repair protein rad51 homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0020330 GCST90088117 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYZAP 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087659 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYZAP 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090476 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYZAP 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090939 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTH1R 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087460 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTH2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089767 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTHLH 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088151 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTK2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088846 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTK2B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086726 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTK2B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090381 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTK6 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088537 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTK7 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090736 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTN 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088204 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTP4A2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086859 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN1 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90088181 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN11 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90086870 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN11 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90088362 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN13 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087136 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN2 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein phosphatase non-receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0020836 GCST90088365 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN4 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087848 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein phosphatase non-receptor type 6 measurement http://www.ebi.ac.uk/efo/EFO_0020837 GCST90088661 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN7 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087907 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPN9 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087113 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRA 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090604 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRD 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090612 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRH 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086620 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRH 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086897 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRJ 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090079 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRN2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087321 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90088942 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICAM5 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90090075 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICOS 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087769 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICOS 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088169 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICOSLG 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088893 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ICOSLG 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090616 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ID1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090690 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086896 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090321 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD11 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087534 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD4 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087532 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086421 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD7 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088576 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD9 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087663 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSME1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089238 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSME3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088960 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMG3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087189 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSPN 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088023 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTCHD3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087500 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTEN 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088536 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTGDS 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086317 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTGFRN 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087188 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTGR1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087516 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTGS2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088508 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTH 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089246 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MZB1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089827 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MZF1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087899 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MZT1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090031 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein N6AMT1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086535 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAAA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088245 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAALAD2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089966 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAB1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087665 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAB2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087604 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NACA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088548 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NADK 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087569 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAGK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088573 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAGPA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086611 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAGS 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086637 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAMPT 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088868 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NANOG 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 homeobox protein nanog measurement http://www.ebi.ac.uk/efo/EFO_0020456 GCST90088038 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAP1L1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087576 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAP1L2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087507 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAPA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088653 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAPB 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087128 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAT1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087112 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NAT14 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086550 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NBL1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088140 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NBR1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089785 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NBR1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089786 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCAM1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088719 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRR 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089365 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRS 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089268 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTPRU 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090137 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTS 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086903 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PTX3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089431 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PUF60 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086350 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PURA 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087056 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PUS1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086605 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PVR 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090023 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PVRIG 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089444 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PXDN 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087456 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PXDNL 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086685 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PXYLP1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089277 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PYDC1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087259 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PYGL 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086748 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PYY 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088497 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PZP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089510 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QDPR 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086641 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QKI 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089766 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QPCT 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089874 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QPCTL 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090347 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QRFP 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089443 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QSOX1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089274 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QSOX1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089300 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein QSOX2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090182 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMGCS2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087622 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMGN1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090542 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMOX2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087987 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMP19 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087426 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNF1A 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086600 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNF4A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086199 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPA1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087006 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPA2B1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089013 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPAB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088693 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPAB 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090367 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPC 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086739 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPDL 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086474 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPF 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090810 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPH1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087862 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPK 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088854 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPM 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087223 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPR 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087489 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HNRNPR 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087495 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HOGA1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086190 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HOMER2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087151 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HP 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088210 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HP 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089914 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HPGD 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088855 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HPGDS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087062 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HPSE 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089086 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NECTIN1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090307 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NECTIN1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090614 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NECTIN2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089318 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NECTIN3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087526 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NECTIN4 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089179 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEDD9 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087277 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEFH 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090898 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEFL 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086223 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEGR1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087379 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEGR1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089633 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEK7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087169 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NELL1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089486 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NELL2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089259 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NENF 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090560 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEO1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090371 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NET1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087850 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NETO1 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089115 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NETO2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086343 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEU1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089256 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEURL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087556 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NEURL4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087459 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NFASC 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089710 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NFATC1 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087857 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NFATC4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086796 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NFE2L1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086573 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C20orf173 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089630 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C21orf33 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089252 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C22orf15 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089645 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C2orf40 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089366 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C2orf66 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089141 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C2orf82 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090691 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90088016 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90088052 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90088053 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90088709 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90088798 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90089212 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3orf18 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089609 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C3orf52 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089954 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C4A;C4B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087923 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C4A;C4B 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088710 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C4BPA 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090695 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C4BPB 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089700 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C4orf32 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090715 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C5 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087935 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088105 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C5;C6 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088711 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C5orf15 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089369 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C5orf38 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089380 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C5orf46 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090509 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C5orf63 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087410 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C6 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 complement component C6 measurement http://www.ebi.ac.uk/efo/EFO_0020281 GCST90088585 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C6orf226 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090035 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C6orf25 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089640 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C6orf25 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090252 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C6orf25 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090704 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C6orf58 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089699 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C6orf89 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086484 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C7 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90087644 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C7 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90088123 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C7orf69 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090746 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C7orf73 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090387 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C8A;C8B;C8G 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087938 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C8G 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087914 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C8orf33 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090779 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C9 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90087635 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C9 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90087931 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C9 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90088215 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088834 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA10 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087595 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA10 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088291 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA11 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090344 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA13 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088376 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088835 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088515 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf162 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089554 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf185 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086397 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf186 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090053 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf198 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090001 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf210 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090042 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf226 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089967 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf43 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089582 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1orf56 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089189 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QA;C1QB;C1QC 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088051 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QBP 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088832 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QC 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087782 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QL1 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089401 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QL2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089418 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QL4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089681 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QTNF1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089348 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QTNF2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090320 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QTNF3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086435 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QTNF3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089765 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QTNF5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089849 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1QTNF9 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089257 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1R 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 complement C1r subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008090 GCST90088290 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1RL 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090646 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1S 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 complement C1s subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008091 GCST90088445 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C1S 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 complement C1s subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008091 GCST90090333 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein C2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 complement C2 measurement http://www.ebi.ac.uk/efo/EFO_0020274 GCST90088254 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHMT1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086918 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SHMT2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087157 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIAE 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090592 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGIRR 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090130 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088699 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC10 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086409 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC10 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089267 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC11 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090379 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC12 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086196 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC12 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090146 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC14 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088943 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC14 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090077 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC15 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086471 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC6 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088041 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC7 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088042 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC8 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089886 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIGLEC9 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088182 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIRPA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089033 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIRPA 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090497 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIRPB1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089319 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIRPB2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089137 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIRPG 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090574 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIRT2 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088884 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIRT5 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087003 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SIT1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086601 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK9 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090008 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINT1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088089 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINT2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088100 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINT3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089929 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPN 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087283 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPOCK1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086767 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPOCK1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089062 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPOCK2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089063 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPOCK3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090901 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPON1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088655 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPON1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089066 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPON2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090051 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPOP 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087640 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087382 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPR 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090608 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPRED1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090125 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPRN 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087446 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPRY1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090729 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPSB1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087672 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPTAN1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088885 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPTLC1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089902 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPTLC2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089772 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SQSTM1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089784 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SRC 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 proto-oncogene tyrosine-protein kinase Src measurement http://www.ebi.ac.uk/efo/EFO_0010927 GCST90089060 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SRI 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086930 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMDT1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090720 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMIM10 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090669 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMIM13 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087450 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMIM24 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089664 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMIM9 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090361 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMOC1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087386 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMOC1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089152 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMPD1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086460 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMPDL3A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087771 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMPDL3A 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088769 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMR3A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089866 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMR3B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090234 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMTN 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087060 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMURF1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086795 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMURF2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087699 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMYD2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087116 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNAI2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086185 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNAP25 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087377 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNAP29 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086931 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNAPIN 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089602 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNCA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090201 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNCA 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090202 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNN 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089814 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNRPA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087146 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNRPF 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089065 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPAG11A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089172 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPAG11B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089204 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPARC 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90087792 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPARC 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90088202 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPARCL1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087624 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPARCL1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088700 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPAST 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086478 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPAST 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090175 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPATA20 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086548 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPATA31D4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090735 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPATA9 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089848 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPDEF 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086183 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPEF1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087285 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPG20 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086579 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPG21 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086552 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPHK1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088654 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPHK2 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088701 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090073 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK13 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086375 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK14 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090232 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087423 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK5 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089995 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089177 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086521 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPINK8 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089953 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STMN3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089991 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STMN4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089330 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STOM 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090088 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STOML2 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089494 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STOX1 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086885 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STUB1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086229 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STUB1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086697 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX10 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087261 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX12 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086256 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX16 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090272 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX18 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090463 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX1A 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088509 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX1B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089596 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089795 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089717 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086398 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX6 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086509 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX7 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090098 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STX8 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086494 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SUDS3 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086413 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SULF2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090116 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SULT1A3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087674 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SULT1B1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087142 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SULT1E1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090882 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SULT2A1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090842 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNTB1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090493 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNU13 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087554 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNX1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089589 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNX1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090310 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNX17 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087264 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNX4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088578 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNX7 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087844 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SNX8 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089572 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOCS3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086747 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOCS7 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086841 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOD1 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088074 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOD2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088866 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOD3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089130 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOD3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090205 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SORBS3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087327 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SORCS2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088749 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SORT1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086672 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOS1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090910 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOST 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087373 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOST 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089175 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SOSTDC1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090069 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPACA1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089307 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPACA3 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090034 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPACA5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089459 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SPACA7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089445 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SRL 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086507 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SRSF6 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086807 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SRSF7 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087330 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SRXN1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087851 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SSB 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087506 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SSB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087570 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SSMEM1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090111 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SSR1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090055 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SSRP1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088886 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SST 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089247 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SSU72 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087530 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST14 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086502 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST3GAL1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089127 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST3GAL2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089336 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST3GAL5 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086356 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST3GAL6 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089586 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST6GAL1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089262 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST6GALNAC1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089889 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST6GALNAC2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089858 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST6GALNAC3 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086376 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST6GALNAC3 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086415 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST6GALNAC5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089930 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST6GALNAC6 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089750 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST8SIA2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089923 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST8SIA3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089574 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC5A5 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087253 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC5A8 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087613 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC6A14 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087350 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC6A16 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087353 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC6A9 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086838 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLC9B2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090500 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLCO5A1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086847 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLITRK1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086432 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLITRK1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088476 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLITRK3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086345 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLITRK4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089686 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLITRK5 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088748 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLMAP 5,321 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089721 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLPI 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088681 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLTM 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090126 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SLURP1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089399 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMAD1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090850 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMAD2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086242 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMAD2 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086700 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMAD3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086241 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMAD4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086907 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMAP1 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086836 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMARCC1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086593 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMC3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087865 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein SMCO2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089928 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST8SIA4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089628 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ST8SIA6 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089575 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAB1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087879 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAB2 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088363 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAMBPL1 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086960 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087035 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAR 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086224 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAT1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086247 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAT1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086927 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAT3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086234 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAT3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086236 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAT6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086248 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAU1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087008 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STAU2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087325 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STC1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088821 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STC2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089310 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STIM1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090380 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STIM1 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090598 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STIP1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089061 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STK16 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088404 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STK17B 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088978 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STK17B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090152 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STK17B 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090184 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STK24 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087100 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein STMN2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086491 Genome-wide genotyping array 2021-04-30 33724339 Wang MH 2021-03-16 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/33724339 Novel Genetic Variant Predicts Surgical Recurrence Risk in Crohn's Disease Patients. Surgical recurrence in Crohn's disease 132 European ancestry cases, 240 European ancestry controls NA Illumina [213386] 1 response to surgery http://www.ebi.ac.uk/efo/EFO_0009951 GCST011589 Targeted genotyping array [ImmunoChip] 2021-06-04 32970095 Clifford RE 2020-09-24 JAMA Otolaryngol Head Neck Surg www.ncbi.nlm.nih.gov/pubmed/32970095 Novel Risk Loci in Tinnitus and Causal Inference With Neuropsychiatric Disorders Among Adults of European Ancestry. Tinnitus 172,995 European ancestry individuals 94,755 European ancestry cases, 166,077 European ancestry controls Affymetrix [up to 96000000] (imputed) 1 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST011785 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.2: Procedure and treatment not carried out because of patient's decision for other and unspecified reasons (Gene-based burden) 2,380 European ancestry cases, 383,365 European ancestry controls NA Illumina [185292] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085275 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - methotrexate 2,438 European ancestry cases, 318,320 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078051 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.8: Procedure and treatment not carried out for other reasons (Gene-based burden) 20,562 European ancestry cases, 358,695 European ancestry controls NA Illumina [185173] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085276 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - metoclopramide 530 European ancestry cases, 320,228 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078087 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.9: Procedure and treatment not carried out, unspecified reason (Gene-based burden) 12,610 European ancestry cases, 358,984 European ancestry controls NA Illumina [185041] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085277 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - metoprolol 841 European ancestry cases, 319,917 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078097 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56: Problems related to employment and unemployment (Gene-based burden) 7,388 European ancestry cases, 365,832 European ancestry controls NA Illumina [185095] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90085282 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H029: Eye or eyelid problem (Gene-based burden) 3,320 European ancestry cases, 325,732 European ancestry controls NA Illumina [184145] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90081719 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured heel right (UKB data field 4096) 545 European ancestry cases, 169,917 European ancestry controls NA Affymetrix, Illumina [283979] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079147 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye trauma (Gene-based burden) 681 European ancestry cases, 331,073 European ancestry controls NA Illumina [184201] 0 eye injury http://www.ebi.ac.uk/efo/EFO_0009485 GCST90081744 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speech reception threshold estimate left (UKB data field 20019) 170,543 European ancestry individuals NA Affymetrix, Illumina [283930] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90078249 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Female infertility (Gene-based burden) 592 European ancestry cases, 331,162 European ancestry controls NA Illumina [184168] 0 female infertility http://www.ebi.ac.uk/efo/EFO_0008560 GCST90081809 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speech reception threshold estimate right (UKB data field 20021) 170,510 European ancestry individuals NA Affymetrix, Illumina [283903] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90078250 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fibromyalgia (Gene-based burden) 854 European ancestry cases, 330,900 European ancestry controls NA Illumina [184201] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90081917 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N40: Benign prostatic hyperplasia 15,936 European ancestry cases, 156,384 European ancestry controls NA Affymetrix, Illumina [283858] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90080617 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79: fibromyalgia (Gene-based burden) 766 European ancestry cases, 328,286 European ancestry controls NA Illumina [184145] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90081918 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 14 (4935) 1,767 European ancestry cases, 168,407 European ancestry controls NA Affymetrix, Illumina [283288] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079230 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture clavicle collar bone (Gene-based burden) 739 European ancestry cases, 331,015 European ancestry controls NA Illumina [184201] 0 clavicle fracture http://www.ebi.ac.uk/efo/EFO_0009614 GCST90081952 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 15 (4935) 165,470 European ancestry cases, 4,704 European ancestry controls NA Affymetrix, Illumina [283288] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079231 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42: fracture clavicle collar bone (Gene-based burden) 576 European ancestry cases, 328,476 European ancestry controls NA Illumina [184145] 0 clavicle fracture http://www.ebi.ac.uk/efo/EFO_0009614 GCST90081953 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 16 (4935) 2,280 European ancestry cases, 167,894 European ancestry controls NA Affymetrix, Illumina [283288] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079232 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture fibula (Gene-based burden) 661 European ancestry cases, 331,093 European ancestry controls NA Illumina [184201] 0 fibula fracture http://www.ebi.ac.uk/efo/EFO_0009613 GCST90081968 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 17 (4935) 881 European ancestry cases, 169,293 European ancestry controls NA Affymetrix, Illumina [283288] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079233 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S824: fracture fibula (Gene-based burden) 574 European ancestry cases, 328,478 European ancestry controls NA Illumina [184145] 0 fibula fracture http://www.ebi.ac.uk/efo/EFO_0009613 GCST90081969 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 13 (4935) 734 European ancestry cases, 169,393 European ancestry controls NA Affymetrix, Illumina [283225] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079229 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40: Inguinal hernia (Gene-based burden) 2,212 European ancestry cases, 326,840 European ancestry controls NA Illumina [184145] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90081899 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by urinary frequency bladder irritability in the last three months - 600 Not bothered at all (UKB data field 21058) 85,424 European ancestry cases, 69,620 European ancestry controls NA Affymetrix, Illumina [262534] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078814 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Iron deficiency anaemia (Gene-based burden) 2,724 European ancestry cases, 329,030 European ancestry controls NA Illumina [184201] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90081773 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by urinary frequency bladder irritability in the last three months - 601 Bothered a little (UKB data field 21058) 51,192 European ancestry cases, 103,852 European ancestry controls NA Affymetrix, Illumina [262534] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078815 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50: iron deficiency anaemia (Gene-based burden) 2,361 European ancestry cases, 326,691 European ancestry controls NA Illumina [184145] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90081774 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by urinary frequency bladder irritability in the last three months - 602 Bothered a lot (UKB data field 21058) 18,428 European ancestry cases, 136,616 European ancestry controls NA Affymetrix, Illumina [262534] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078816 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Irregular heart beat (Gene-based burden) 1,046 European ancestry cases, 330,708 European ancestry controls NA Illumina [184201] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90081883 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Every day (UKB data field 21025) 3,727 European ancestry cases, 151,293 European ancestry controls NA Affymetrix, Illumina [262498] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078694 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49: irregular heart beat (Gene-based burden) 943 European ancestry cases, 328,109 European ancestry controls NA Illumina [184145] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90081884 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Less than one day a month (UKB data field 21025) 30,431 European ancestry cases, 124,589 European ancestry controls NA Affymetrix, Illumina [262498] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078689 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Irritable bowel syndrome (Gene-based burden) 11,343 European ancestry cases, 320,411 European ancestry controls NA Illumina [184201] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90081685 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - More than one day a week (UKB data field 21025) 13,542 European ancestry cases, 141,478 European ancestry controls NA Affymetrix, Illumina [262498] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078693 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58: Irritable bowel syndrome (Gene-based burden) 9,503 European ancestry cases, 319,549 European ancestry controls NA Illumina [184145] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90081686 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Never (UKB data field 21025) 71,454 European ancestry cases, 83,566 European ancestry controls NA Affymetrix, Illumina [262498] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078688 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Jaundice unknown cause (Gene-based burden) 630 European ancestry cases, 331,124 European ancestry controls NA Illumina [184201] 0 Jaundice http://purl.obolibrary.org/obo/HP_0000952 GCST90081893 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - One day a month (UKB data field 21025) 10,030 European ancestry cases, 144,990 European ancestry controls NA Affymetrix, Illumina [262498] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078690 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R17: jaundice unknown cause (Gene-based burden) 557 European ancestry cases, 328,495 European ancestry controls NA Illumina [184145] 0 Jaundice http://purl.obolibrary.org/obo/HP_0000952 GCST90081894 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - One day a week (UKB data field 21025) 5,396 European ancestry cases, 149,624 European ancestry controls NA Affymetrix, Illumina [262498] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078692 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Joint disorder (Gene-based burden) 2,082 European ancestry cases, 329,672 European ancestry controls NA Illumina [184201] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90081759 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Two to three days a month (UKB data field 21025) 20,440 European ancestry cases, 134,580 European ancestry controls NA Affymetrix, Illumina [262498] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078691 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: joint disorder (Gene-based burden) 1,757 European ancestry cases, 327,295 European ancestry controls NA Illumina [184145] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90081760 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Currently in last three months suffer from abdominal pain (UKB data field 21035) 45,104 European ancestry cases, 109,755 European ancestry controls NA Affymetrix, Illumina [262312] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078732 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Joint pain (Gene-based burden) 2,226 European ancestry cases, 329,528 European ancestry controls NA Illumina [184201] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90081911 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Currently suffer from abdominal distension (UKB data field 21038) 36,054 European ancestry cases, 118,772 European ancestry controls NA Affymetrix, Illumina [262204] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078753 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: joint pain (Gene-based burden) 1,766 European ancestry cases, 327,286 European ancestry controls NA Illumina [184145] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90081912 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49: heart arrhythmia (Gene-based burden) 2,296 European ancestry cases, 326,756 European ancestry controls NA Illumina [184145] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90081646 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain in arms legs joints in the past three months - 602 Bothered a lot (UKB data field 21049) 32,509 European ancestry cases, 122,604 European ancestry controls NA Affymetrix, Illumina [262645] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078790 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart attack myocardial infarction (Gene-based burden) 10,448 European ancestry cases, 321,306 European ancestry controls NA Illumina [184201] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90081643 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by dizziness in the last three months - 600 Not bothered at all (UKB data field 21053) 113,250 European ancestry cases, 41,873 European ancestry controls NA Affymetrix, Illumina [262644] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078800 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21: heart attack myocardial infarction (Gene-based burden) 9,479 European ancestry cases, 319,573 European ancestry controls NA Illumina [184145] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90081644 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by dizziness in the last three months - 601 Bothered a little (UKB data field 21053) 38,621 European ancestry cases, 116,502 European ancestry controls NA Affymetrix, Illumina [262644] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078801 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart cardiac problem (Gene-based burden) 1,496 European ancestry cases, 330,258 European ancestry controls NA Illumina [184201] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90081633 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by dizziness in the last three months - 602 Bothered a lot (UKB data field 21053) 3,252 European ancestry cases, 151,871 European ancestry controls NA Affymetrix, Illumina [262644] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078802 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I52: heart cardiac problem (Gene-based burden) 1,442 European ancestry cases, 327,610 European ancestry controls NA Illumina [184145] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90081634 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling tired all the time in the last three months - 600 Not bothered at all (UKB data field 21060) 53,698 European ancestry cases, 101,431 European ancestry controls NA Affymetrix, Illumina [262637] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078820 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart valve problem or heart murmur (Gene-based burden) 3,129 European ancestry cases, 328,625 European ancestry controls NA Illumina [184201] 0 Abnormal cardiovascular system physiology http://purl.obolibrary.org/obo/HP_0011025 GCST90081647 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling tired all the time in the last three months - 601 Bothered a little (UKB data field 21060) 76,420 European ancestry cases, 78,709 European ancestry controls NA Affymetrix, Illumina [262637] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078821 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R01: heart valve problem or heart murmur (Gene-based burden) 2,752 European ancestry cases, 326,300 European ancestry controls NA Illumina [184145] 0 Abnormal cardiovascular system physiology http://purl.obolibrary.org/obo/HP_0011025 GCST90081648 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling tired all the time in the last three months - 602 Bothered a lot (UKB data field 21060) 25,011 European ancestry cases, 130,118 European ancestry controls NA Affymetrix, Illumina [262637] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078822 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Helicobacter pylori (Gene-based burden) 1,375 European ancestry cases, 330,379 European ancestry controls NA Illumina [184201] 0 Helicobacter pylori http://purl.obolibrary.org/obo/NCBITaxon_210 GCST90081835 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by trouble sleeping in the last three months - 600 Not bothered at all (UKB data field 21061) 52,659 European ancestry cases, 102,465 European ancestry controls NA Affymetrix, Illumina [262634] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078823 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B98: helicobacter pylori (Gene-based burden) 1,318 European ancestry cases, 327,734 European ancestry controls NA Illumina [184145] 0 Helicobacter pylori http://purl.obolibrary.org/obo/NCBITaxon_210 GCST90081836 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by trouble sleeping in the last three months - 601 Bothered a little (UKB data field 21061) 75,649 European ancestry cases, 79,475 European ancestry controls NA Affymetrix, Illumina [262634] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078824 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hepatitis (Gene-based burden) 506 European ancestry cases, 331,248 European ancestry controls NA Illumina [184201] 0 Hepatitis http://purl.obolibrary.org/obo/HP_0012115 GCST90081687 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by trouble sleeping in the last three months - 602 Bothered a lot (UKB data field 21061) 26,816 European ancestry cases, 128,308 European ancestry controls NA Affymetrix, Illumina [262634] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078825 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hiatus hernia (Gene-based burden) 10,744 European ancestry cases, 321,010 European ancestry controls NA Illumina [184201] 0 Hiatus hernia http://purl.obolibrary.org/obo/HP_0002036 GCST90081871 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by chest pain in the last three months - 600 Not bothered at all (UKB data field 21052) 133,883 European ancestry cases, 21,225 European ancestry controls NA Affymetrix, Illumina [262627] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078797 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K44: hiatus hernia (Gene-based burden) 9,911 European ancestry cases, 319,141 European ancestry controls NA Illumina [184145] 0 Hiatus hernia http://purl.obolibrary.org/obo/HP_0002036 GCST90081872 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by chest pain in the last three months - 601 Bothered a little (UKB data field 21052) 19,597 European ancestry cases, 135,511 European ancestry controls NA Affymetrix, Illumina [262627] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078798 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High cholesterol (Gene-based burden) 57,365 European ancestry cases, 274,389 European ancestry controls NA Illumina [184201] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90081869 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40: epilepsy (Gene-based burden) 3,248 European ancestry cases, 325,804 European ancestry controls NA Illumina [184145] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90081730 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - develop (UKB data field 4957) 7,895 European ancestry cases, 163,430 European ancestry controls NA Affymetrix, Illumina [284819] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079237 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Essential hypertension (Gene-based burden) 2,954 European ancestry cases, 328,800 European ancestry controls NA Illumina [184201] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90081637 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - grow (UKB data field 4957) 18,400 European ancestry cases, 152,925 European ancestry controls NA Affymetrix, Illumina [284819] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079236 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I10: essential hypertension (Gene-based burden) 2,588 European ancestry cases, 326,464 European ancestry controls NA Illumina [184145] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90081638 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48: Other disorders of penis 3,394 European ancestry cases, 169,501 European ancestry controls NA Affymetrix, Illumina [284683] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90080631 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye or eyelid problem (Gene-based burden) 3,583 European ancestry cases, 328,171 European ancestry controls NA Illumina [184201] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90081718 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever unenthusiastic/disinterested for a whole week (UKB data field 4631) 63,612 European ancestry cases, 107,337 European ancestry controls NA Affymetrix, Illumina [284368] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90079213 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fybogel orange s/f granules 947 European ancestry cases, 319,811 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078214 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z42: Encounter for plastic and reconstructive surgery following medical procedure or healed injury (Gene-based burden) 2,861 European ancestry cases, 385,069 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085244 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gabapentin 2,240 European ancestry cases, 318,518 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078068 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z42.1: Encounter for breast reconstruction following mastectomy (Gene-based burden) 2,185 European ancestry cases, 385,745 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085243 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - garlic product 5,915 European ancestry cases, 314,843 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078146 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z43: Encounter for attention to artificial openings (Gene-based burden) 2,178 European ancestry cases, 385,749 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085246 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gaviscon liquid 2,498 European ancestry cases, 318,260 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078029 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z43.2: Encounter for attention to ileostomy (Gene-based burden) 1,010 European ancestry cases, 386,920 European ancestry controls NA Illumina [185344] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085245 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ginkgo forte tablet 2,502 European ancestry cases, 318,256 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078147 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45: Encounter for adjustment and management of implanted device (Gene-based burden) 4,136 European ancestry cases, 383,784 European ancestry controls NA Illumina [185344] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90085250 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ginseng product 633 European ancestry cases, 320,125 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078148 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45.0: Encounter for adjustment and management of cardiac device (Gene-based burden) 1,115 European ancestry cases, 386,805 European ancestry controls NA Illumina [185344] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90085247 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gliclazide 3,820 European ancestry cases, 316,938 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078072 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45.2: Encounter for adjustment and management of vascular access device (Gene-based burden) 1,644 European ancestry cases, 386,286 European ancestry controls NA Illumina [185344] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90085248 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - glucosamine product 29,647 European ancestry cases, 291,111 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078223 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45.8: Encounter for adjustment and management of other implanted devices (Gene-based burden) 1,272 European ancestry cases, 386,658 European ancestry controls NA Illumina [185344] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90085249 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - glyceryl trinitrate 1,422 European ancestry cases, 319,336 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078000 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Very unhappy (UKB data field 4570) 792 European ancestry cases, 174,985 European ancestry controls NA Affymetrix, Illumina [290804] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90079204 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32: Chronic sinusitis (Gene-based burden) 2,961 European ancestry cases, 326,091 European ancestry controls NA Illumina [184145] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90081823 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes now most or all of the time (UKB data field 4803) 12,999 European ancestry cases, 161,792 European ancestry controls NA Affymetrix, Illumina [289523] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079220 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Colitis not crohns or ulcerative colitis (Gene-based burden) 1,203 European ancestry cases, 330,551 European ancestry controls NA Illumina [184201] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90081851 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes now a lot of the time (UKB data field 4803) 5,305 European ancestry cases, 169,486 European ancestry controls NA Affymetrix, Illumina [289523] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079221 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52: colitis not crohns or ulcerative colitis (Gene-based burden) 1,104 European ancestry cases, 327,948 European ancestry controls NA Illumina [184145] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90081852 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes now some of the time (UKB data field 4803) 17,452 European ancestry cases, 157,339 European ancestry controls NA Affymetrix, Illumina [289523] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079222 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Constipation (Gene-based burden) 601 European ancestry cases, 331,153 European ancestry controls NA Illumina [184201] 0 Constipation http://purl.obolibrary.org/obo/HP_0002019 GCST90081943 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes but not now but have in the past (UKB data field 4803) 20,407 European ancestry cases, 154,384 European ancestry controls NA Affymetrix, Illumina [289523] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079223 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59: constipation (Gene-based burden) 500 European ancestry cases, 328,552 European ancestry controls NA Illumina [184145] 0 Constipation http://purl.obolibrary.org/obo/HP_0002019 GCST90081944 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Shortness of breath walking on level ground (UKB data field 4717) 18,321 European ancestry cases, 156,558 European ancestry controls NA Affymetrix, Illumina [289433] 0 shortness of breath http://www.ebi.ac.uk/efo/EFO_0009727 GCST90079217 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Crohns disease (Gene-based burden) 1,324 European ancestry cases, 330,430 European ancestry controls NA Illumina [184201] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90081855 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48.8: Other specified disorders of penis 524 European ancestry cases, 175,725 European ancestry controls NA Affymetrix, Illumina [288904] 0 penile disorder http://purl.obolibrary.org/obo/MONDO_0002036 GCST90080630 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50: crohns disease (Gene-based burden) 1,250 European ancestry cases, 327,802 European ancestry controls NA Illumina [184145] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90081856 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever depressed for a whole week (UKB data field 4598) 94,987 European ancestry cases, 79,419 European ancestry controls NA Affymetrix, Illumina [288884] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90079211 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.9: Encounter for screening, unspecified (Gene-based burden) 24,217 European ancestry cases, 317,766 European ancestry controls NA Illumina [184487] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085205 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diclofenac 9,113 European ancestry cases, 311,645 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078117 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z22: Carrier of infectious disease (Gene-based burden) 1,553 European ancestry cases, 386,247 European ancestry controls NA Illumina [185343] 0 carrier status http://www.ebi.ac.uk/efo/EFO_0007658 GCST90085208 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dicloflex 512 European ancestry cases, 320,246 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078155 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z22.3: Carrier of other specified bacterial diseases (Gene-based burden) 1,238 European ancestry cases, 386,591 European ancestry controls NA Illumina [185343] 0 carrier status http://www.ebi.ac.uk/efo/EFO_0007658 GCST90085207 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - digoxin 1,185 European ancestry cases, 319,573 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078240 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z23: Encounter for immunization (Gene-based burden) 20,430 European ancestry cases, 341,925 European ancestry controls NA Illumina [184935] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90085209 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dihydrocodeine 1,534 European ancestry cases, 319,224 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078116 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28: Immunization not carried out and underimmunization status (Gene-based burden) 6,544 European ancestry cases, 366,674 European ancestry controls NA Illumina [185085] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90085214 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diltiazem 909 European ancestry cases, 319,849 European ancestry controls NA Affymetrix, Illumina [447992] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078096 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. C-reactive protein levels 8,318 European ancestry individuals NA Illumina [~ 9000000] (imputed) 2 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011919 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Erythropoietin levels 8,318 European ancestry individuals NA Illumina [~ 9000000] (imputed) 1 erythropoetin measurement http://www.ebi.ac.uk/efo/EFO_0008391 GCST011918 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. IgA levels 8,318 European ancestry individuals NA Illumina [~ 9000000] (imputed) 1 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST011917 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Interleukin-18 levels 8,318 European ancestry individuals (see Ahola-Olli 2017) Illumina [~ 9000000] (imputed) 4 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST011916 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Monocyte chemoattractant protein-1 levels 8,318 European ancestry individuals (see Ahola-Olli 2017) Illumina [~ 9000000] (imputed) 10 CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004749 GCST011915 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. S100 calcium-binding protein levels 8,318 European ancestry individuals 1,141 European ancestry individuals Illumina [~ 9000000] (imputed) 1 S100 calcium-binding protein B measurement http://www.ebi.ac.uk/efo/EFO_0600012 GCST011914 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Thymus and reactivation regulated chemokine levels 8,318 European ancestry individuals NA Illumina [~ 9000000] (imputed) 4 CCL17 measurement http://www.ebi.ac.uk/efo/EFO_0009414 GCST011913 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Vascular endothelial growth factor A levels 8,318 European ancestry individuals (see Ahola-Olli 2017) Illumina [~ 9000000] (imputed) 5 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST011912 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Brain-derived neurotrophic factor levels 8,318 European ancestry individuals 1,141 European ancestry individuals Illumina [~ 9000000] (imputed) 0 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST011911 Genome-wide genotyping array 2021-06-17 33227023 Wang Y 2020-11-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33227023 Genome-wide association study identifies 16 genomic regions associated with circulating cytokines at birth. Interleukin-8 levels 8,318 European ancestry individuals 1,141 European ancestry individuals Illumina [~ 9000000] (imputed) 0 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST011910 Genome-wide genotyping array 2021-04-16 33514863 Nishiguchi KM 2021-01-29 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33514863 A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa. Retinitis pigmentosa 432 Japanese ancestry cases, 603 Japanese ancestry controls NA Illumina [10673864] (imputed) 8 retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0019200 GCST90011892 Genome-wide genotyping array 2021-04-16 33514863 Nishiguchi KM 2021-01-29 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33514863 A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa. Retinitis pigmentosa 208 Japanese ancestry cases, 287 Japanese ancestry controls NA Illumina [10383808] (imputed) 2 retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0019200 GCST90011893 Genome-wide genotyping array 2021-04-16 33514863 Nishiguchi KM 2021-01-29 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33514863 A hypomorphic variant in EYS detected by genome-wide association study contributes toward retinitis pigmentosa. Retinitis pigmentosa 640 Japanese ancestry cases, 890 Japanese ancestry controls NA Illumina [11309118] (imputed) 13 retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0019200 GCST90011894 Genome-wide genotyping array 2022-07-19 35320353 Kulyte A 2022-03-23 Diabetes www.ncbi.nlm.nih.gov/pubmed/35320353 Genome-wide Association Study Identifies Genetic Loci Associated with Fat Cell Number and Overlap with Genetic Risk Loci For Type 2 Diabetes. Abdominal fat cell number 896 individuals NA NR [9714326] 141 abdominal fat cell number http://www.ebi.ac.uk/efo/EFO_0021534 GCST90104785 Genome-wide genotyping array 2020-12-10 32959083 Adewuyi EO 2020-09-21 Hum Genet www.ncbi.nlm.nih.gov/pubmed/32959083 Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality. Endometriosis or depression (pleiotropy) 17,054 endometriosis cases, 170,756 European ancestry depression cases, 191,858 controls, 329,443 European ancestry controls NA NR [6694342] 31 endometriosis, unipolar depression http://www.ebi.ac.uk/efo/EFO_0001065, http://www.ebi.ac.uk/efo/EFO_0003761 GCST010859 Genome-wide genotyping array 2020-12-09 32968195 Nakamura R 2020-09-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32968195 A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis 1,173 Japanese cases, 8.925 Japanese controls, 20,806 European ancestry cases, 53,439 European ancestry controls 1,234 Chinese ancestry cases, 2,850 Chinese ancestry controls, 707Japanese ancestry cases, 971 Japanese ancestry controls Illumina [4249201] (imputed) 1 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST010857 Genome-wide genotyping array 2021-05-18 33979322 Currant H 2021-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33979322 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images. Retinal nerve fibre layer (RNFL) thickness 31,434 European ancestry individuals NA Affymetrix [9231066] (imputed) 32 retinal nerve fibre layer thickness measurement http://www.ebi.ac.uk/efo/EFO_0600004 GCST90014266 Genome-wide genotyping array 2021-05-18 33979322 Currant H 2021-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33979322 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images. Ganglion cell inner plexiform layer (GCIPL) thickness 31,434 European ancestry individuals NA Affymetrix [9231066] (imputed) 23 ganglion cell inner plexiform layer thickness measurement http://www.ebi.ac.uk/efo/EFO_0600005 GCST90014267 Genome-wide genotyping array 2021-05-18 33979322 Currant H 2021-05-12 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33979322 Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography images. Retinal nerve fibre layer thickness or ganglion cell inner plexiform layer thickness (MTAG) 31,434 European ancestry individuals NA Affymetrix [9231066] (imputed) 46 retinal layer thickness measurement http://www.ebi.ac.uk/efo/EFO_0600002 GCST011676 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL11 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-11 measurement http://www.ebi.ac.uk/efo/EFO_0020490 GCST90088715 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL11RA 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-11 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020491 GCST90088526 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP1B3 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090431 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP1B4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090919 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP2A3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087493 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP4B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090953 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP5B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088831 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP5J 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089833 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP5J2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086783 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP5O 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090551 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATRAID 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086462 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AURKA 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088231 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AURKB 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088330 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AXIN2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087308 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AXIN2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090197 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AXL 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086349 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AZGP1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090622 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AZU1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087916 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AZU1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088049 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B2M 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088413 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GALT1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090744 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GALT2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086831 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GALT6 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089963 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GAT3 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089555 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GLCT 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089173 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GNT2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089962 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GNT6 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089649 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B3GNT8 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090613 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GALNT1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090422 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GALT1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087411 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GALT2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090770 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GALT3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089570 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GALT5 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086261 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GALT6 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086466 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein B4GALT7 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089846 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FMOD 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089371 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FMR1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089787 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FMR1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089788 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FMR1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089790 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FN1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088383 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FN1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088384 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FN1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088589 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FNDC4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087449 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FNDC5 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090007 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOLH1 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088278 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOLH1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089052 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOLR3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089101 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOXC2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087744 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOXG1 5,314 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090894 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FOXJ2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087833 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGFLR1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089759 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHA1;IGHA2;JCHAIN;IGL;IGK;PIGR 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086533 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHA1;IGHA2;JCHAIN;IGL;IGK;PIGR 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090220 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHD;IGL;IGK 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088812 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHE;IGL;IGK 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088593 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHG1;IGHG2;IGHG3;IGHG4;IGL;IGK 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088044 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHG1;IGHG2;IGHG3;IGHG4;IGL;IGK 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088489 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHG2 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087400 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHG4 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087401 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGHM;JCHAIN;IGL;IGK 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088220 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGLL1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089456 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGLON5 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089453 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGSF11 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086410 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGSF11 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090603 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGSF3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090783 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGSF8 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089603 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGSF9 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086319 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IGSF9B 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090480 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IK 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089737 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL10 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90087636 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL10 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90088063 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL10RA 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086233 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL10RA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090054 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL10RA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090813 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL10RB 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-10 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0010786 GCST90087991 Genome-wide genotyping array 2021-09-08 33838163 Luo S 2021-04-07 Kidney Int www.ncbi.nlm.nih.gov/pubmed/33838163 Genome-wide association study of serum metabolites in the African American Study of Kidney Disease and Hypertension. Serum metabolite concentrations in chronic kidney disease 619 African American individuals NA Illumina [14760605] (imputed) 42 serum metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005653 GCST012353 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAMP 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088424 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAPLN1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088261 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAPLN4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089437 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAT1 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088109 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAVCR1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090453 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAVCR2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086765 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAVCR2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088950 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAVCR2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089697 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBA1;HBB 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088811 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBD 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089607 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBE1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089683 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBE1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 8 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089684 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBEGF 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087777 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBEGF 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088592 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBG1 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086395 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBQ1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089955 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HBZ 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089568 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HCAR2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087480 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HCK 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase HCK measurement http://www.ebi.ac.uk/efo/EFO_0020824 GCST90088349 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HCN1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087218 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HDAC8 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088110 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HDGF 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090404 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HDGFRP2 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088737 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HDHD2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087461 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HDLBP 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087533 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNER 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 delta/notch like EGF Repeat Containing protein measurement http://www.ebi.ac.uk/efo/EFO_0010781 GCST90086749 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNER 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 delta/notch like EGF Repeat Containing protein measurement http://www.ebi.ac.uk/efo/EFO_0010781 GCST90090814 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNM2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086806 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DOC2B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089973 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DOCK9 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087709 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DOK2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087845 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DOT1L 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087158 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPEP1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086323 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPEP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090302 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPEP2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090131 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPP10 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089905 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPP7 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088456 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPP7 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090142 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPT 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088840 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPY30 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087673 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPYSL2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087531 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPYSL3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087173 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DPYSL5 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087149 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DRAXIN 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089651 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DRGX 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090000 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSC1 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086483 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSC2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087392 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSC3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088841 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSCAM 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090534 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSG1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088161 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTK1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087463 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTM1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089754 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTM3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090796 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTO1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086982 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087538 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTP1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088807 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTT2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086652 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GTF2I 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087558 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GUCA1A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086179 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GUCA2B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089303 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GUCY2C 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086293 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GXYLT1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090063 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GYPA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090678 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GZMA 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087628 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GZMA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088387 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GZMB 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087736 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GZMB 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088591 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GZMH 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088348 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GZMK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090747 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GZMM 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089158 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein H1FX 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087175 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein H2AFZ 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088618 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein H6PD 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089703 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HAAO 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089225 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HABP4 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086457 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HECW1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087140 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HEG1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090398 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HEPACAM 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090312 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HEPACAM2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089501 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HEPACAM2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090518 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HEPHL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089360 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HERC1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087171 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HERC4 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089883 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HERC5 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087312 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HERPUD2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090820 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HEXB 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089275 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HEXIM2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087834 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HFE2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088322 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HGD 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090845 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HGF 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90088014 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HGFAC 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088461 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HGFAC 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090172 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HGS 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087580 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HHIP 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086467 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HHLA2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087808 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIBADH 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088754 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIBCH 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086956 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIF1A 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087366 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIKESHI 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090261 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HINT1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089234 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DMPK 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090445 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAI1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086727 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJA2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086808 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJA4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090793 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB1 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088546 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB11 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089665 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB12 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089980 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB14 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090003 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB14 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090016 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB2 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086745 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086818 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJB9 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086614 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC10 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090110 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC11 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090821 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC15 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089728 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC16 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086279 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC17 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087898 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC18 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089999 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC19 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088730 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC27 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087235 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC30 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089888 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089988 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNAJC4 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090250 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNASE1L2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089351 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DNASE2B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089482 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HINT2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089092 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIPK3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088389 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIST1H1C 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088168 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIST1H3A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087816 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIST2H2BE 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087814 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HIST3H2A 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087815 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HK1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087395 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HK2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087394 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HLA-DMA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086384 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HLA-DPB1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090274 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HLA-DQA2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089811 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HLA-DRB3 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089593 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRDX4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089834 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRDX5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088874 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRDX6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088875 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRELP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089139 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PREP 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087854 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRG2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089768 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRG3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090449 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRH2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086307 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRIM1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087547 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKAA1;PRKAB1;PRKAG1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088955 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKAA2;PRKAB2;PRKAG1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088974 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKACA 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088401 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKAR1B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087014 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088002 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCB 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089050 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCD 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088115 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCG 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089051 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRDX3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090151 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCI 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088352 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCQ 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088528 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCSH 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089145 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKCZ 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088003 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRKG1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087357 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRL 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086519 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRL 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087968 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRLH 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089485 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRLR 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088935 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRLR 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090564 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRMT3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087162 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRNP 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089487 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PROC 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088150 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PROC 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088506 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PROC 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088507 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PROK1 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087911 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PROK1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087929 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PROK2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086438 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PROS1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088025 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRPF6 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090446 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSG2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088901 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSG2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090712 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DSG3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086677 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DTX1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086740 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DTX3L 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086832 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUS2 5,327 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087490 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP13 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089476 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP15 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087260 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP16 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087891 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP26 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090415 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP28 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090923 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP3 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 dual specificity protein phosphatase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020336 GCST90088410 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086194 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUSP6 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086921 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DUT 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090954 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DVL2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087537 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DYNAP 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086405 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DYNLL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088564 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DYNLL2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086769 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DYNLRB1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088543 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DYNLT1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087868 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSN 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088771 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTA1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086989 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTA3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088853 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GSTA4 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087897 Genome-wide genotyping array 2021-04-06 33772158 Hoggart C 2021-03-26 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33772158 Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease. Kawasaki disease 400 European ancestry cases, 6,101 European ancestry controls 346 European ancestry cases, 1,609 European ancestry controls Illumina [5784964] (imputed) 8 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST90013537 Genome-wide genotyping array 2021-04-06 33772158 Hoggart C 2021-03-26 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33772158 Identification of novel locus associated with coronary artery aneurysms and validation of loci for susceptibility to Kawasaki disease. Coronary artery aneurysm in Kawasaki disease 200 European ancestry cases, 276 European ancestry controls NA Illumina [4873589] (imputed) 6 coronary aneurysm http://www.ebi.ac.uk/efo/EFO_1000881 GCST90013538 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Methylsuccinoylcarnitine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026202 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Myo-inositol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026203 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetyl-3-methylhistidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026204 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetyl-aspartyl-glutamate (naag) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026205 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetyl-beta-alanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026206 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetyl-isoputreanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026207 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylalanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026208 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylarginine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026209 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylasparagine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026210 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylaspartate (naa) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026211 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylglucosamine/n-acetylgalactosamine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026212 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylglutamate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026213 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylglutamine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026214 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylglycine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026215 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylhistidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026216 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylisoleucine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026217 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylleucine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026218 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylmethionine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026219 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylneuraminate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026220 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylphenylalanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026221 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylputrescine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026222 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylserine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026223 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetyltaurine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026224 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylthreonine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026225 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-acetylvaline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026226 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-delta-acetylornithine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026227 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-formylanthranilic acid levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026228 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-formylmethionine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026229 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N-trimethyl 5-aminovalerate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026230 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N1-methyl-2-pyridone-5-carboxamide levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026231 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N1-methyladenosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026232 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N1-methylinosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026233 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N2,n2-dimethylguanosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026234 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N6,n6,n6-trimethyllysine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026235 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N6-carbamoylthreonyladenosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026236 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. N6-succinyladenosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026237 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Nicotinamide riboside levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026238 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. O-sulfo-l-tyrosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026239 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Octanoylcarnitine (c8) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026240 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Orotate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026241 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Orotidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026242 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Oxalate (ethanedioate) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026243 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026244 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Palmitoyl sphingomyelin (d18:1/16:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026245 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Pantothenate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026246 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Phenol sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026247 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Phenylacetylglutamine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026248 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Phenylalanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026249 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Phenyllactate (pla) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026250 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Pipecolate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026251 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-(4-hydroxyphenyl)lactate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026077 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026078 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxy-2-ethylpropionate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026079 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxy-3-methylglutarate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026080 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxybutyrate (bhba) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026081 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxyhexanoate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026082 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxyoctanoate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026083 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxypyridine sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026084 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-hydroxystachydrine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026085 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methoxytyramine sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026086 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methoxytyrosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026087 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methyl-2-oxobutyrate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026088 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methyl-2-oxovalerate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026089 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methylglutaconate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026090 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methylglutarylcarnitine (2) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026091 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methylhistidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026092 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-methylxanthine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026093 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 3-ureidopropionate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026094 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 4-acetamidobutanoate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026095 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 4-methyl-2-oxopentanoate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026096 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 4-methylcatechol sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026097 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5,6-dihydrothymine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026098 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5,6-dihydrouridine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026099 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5-acetylamino-6-amino-3-methyluracil levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026100 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5-hydroxyhexanoate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026101 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Dimethylarginine (sdma + adma) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026152 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Dimethylmalonic acid levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026153 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Dopamine 3-o-sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026154 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ergothioneine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026155 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Erythritol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026156 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Erythronate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026157 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ethylmalonate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026158 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Fructose levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026159 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Galactonate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026160 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Galactosylglycerol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026161 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gamma-glutamyl-alpha-lysine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026162 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gamma-glutamylglutamine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026163 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gamma-glutamylleucine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026164 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gamma-glutamylphenylalanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026165 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gamma-glutamylthreonine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026166 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gamma-glutamylvaline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026167 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gluconate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026168 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glutamate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026169 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glutamine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026170 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glutarylcarnitine (c5-dc) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026171 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glycerate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026172 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glycerol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026173 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Glycerophosphoinositol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026174 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Guaiacol sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026175 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Guanosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026176 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Behenoyl sphingomyelin (d18:1/22:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026127 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Benzoate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026128 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Beta-alanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026129 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Beta-citrylglutamate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026130 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Beta-hydroxyisovalerate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026131 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Betaine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026132 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. C-glycosyltryptophan levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026133 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Caffeine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026134 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Carboxyethyl-gaba levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026135 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Carnitine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026136 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Catechol sulfate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026137 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Choline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026138 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Choline phosphate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026139 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Citramalate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026140 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Citrate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026141 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cortisone levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026142 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Creatine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026143 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cys-gly, oxidized levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026144 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cysteine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026145 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cysteinylglycine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026146 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cysteinylglycine disulfide levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026147 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Cytidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026148 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Deoxycarnitine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026149 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Diglycerol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026150 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Dimethyl sulfone levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026151 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Gulonate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026177 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Hippurate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026178 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Histidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026179 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Homoarginine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026180 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Homocarnosine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026181 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Homostachydrine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026182 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Homovanillate (hva) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026183 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Hydroxy-cmpf levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026184 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Hydroxyasparagine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026185 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Indoleacetate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026186 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Isobutyrylcarnitine (c4) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026187 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Isocitrate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026188 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Isoleucine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026189 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Isovalerate (i5:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026190 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Kynurenate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026191 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Leucine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026192 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Maleate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026193 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Mannitol/sorbitol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026194 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Mannose levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026195 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Methionine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026196 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Methionine sulfone levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026197 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Methionine sulfoxide levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026198 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Methyl glucopyranoside (alpha + beta) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026199 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Methylmalonate (mma) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026200 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Methylsuccinate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026201 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5-hydroxyindoleacetate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026102 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5-methylcytidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026103 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5-methylthioadenosine (mta) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026104 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 5-methyluridine (ribothymidine) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026105 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 6-oxopiperidine-2-carboxylate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026106 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026107 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 7-methylguanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026108 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 7-methylxanthine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026109 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Acetylcarnitine (c2) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026110 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Acisoga levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026111 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Adenine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026112 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Adenosine 3',5'-cyclic monophosphate (camp) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026113 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Alanine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026114 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Alpha-hydroxyisocaproate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026115 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Alpha-hydroxyisovalerate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026116 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Alpha-ketoglutaramate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026117 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Alpha-tocopherol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026118 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Arabinose levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026119 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Arabitol/xylitol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026120 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Arabonate/xylonate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026121 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Arachidonate (20:4n6) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026122 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Argininate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026123 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Arginine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026124 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Argininosuccinate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026125 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ascorbate (vitamin c) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026126 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Propionylcarnitine (c3) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026252 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Pseudouridine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026253 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Pyridoxal levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026254 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Pyridoxate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026255 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Pyruvate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026256 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Quinate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026257 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ribitol levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026258 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ribonate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026259 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Ribulonate/xylulonate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026260 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. S-1-pyrroline-5-carboxylate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026261 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. S-methylcysteine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026262 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Salicylate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026263 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Serine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026264 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Spermidine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026265 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Stachydrine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026266 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Stearoyl sphingomyelin (d18:1/18:0) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026267 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Succinimide levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026268 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Succinylcarnitine (c4-dc) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026269 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Tartarate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026270 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Tartronate (hydroxymalonate) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026271 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Theobromine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026272 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Theophylline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026273 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Thioproline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026274 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Threonate levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026275 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Threonine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026276 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Trans-4-hydroxyproline levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026277 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Trigonelline (n'-methylnicotinate) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026278 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Trimethylamine n-oxide levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026279 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Tryptophan levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026280 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Tryptophan betaine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026281 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Uracil levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026282 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Urea levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026283 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. Valine levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026284 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-10457 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026285 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-11261 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026286 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. 2,3-dihydroxy-5-methylthio-4-pentenoate (dmtpa) levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026287 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-11612 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026288 Genome-wide genotyping array 2021-08-24 33437055 Panyard DJ 2021-01-12 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33437055 Cerebrospinal fluid metabolomics identifies 19 brain-related phenotype associations. X-11787 levels 291 European ancestry individuals NA Illumina [7049691] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90026289 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetes (Gene-based burden) 17,927 European ancestry cases, 313,827 European ancestry controls NA Illumina [184201] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90081708 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N43: Hydrocele and spermatocele 1,816 European ancestry cases, 173,556 European ancestry controls NA Affymetrix, Illumina [287765] 0 testicular hydrocele, spermatocele http://www.ebi.ac.uk/efo/EFO_1001859, http://www.ebi.ac.uk/efo/EFO_1001189 GCST90080624 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E14: diabetes (Gene-based burden) 16,961 European ancestry cases, 312,091 European ancestry controls NA Illumina [184145] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90081709 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48.1: Balanitis 591 European ancestry cases, 174,673 European ancestry controls NA Affymetrix, Illumina [287683] 0 balanitis http://www.ebi.ac.uk/efo/EFO_1000833 GCST90080628 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetic eye disease (Gene-based burden) 995 European ancestry cases, 330,759 European ancestry controls NA Illumina [184201] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90081738 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N41: Inflammatory diseases of prostate 2,279 European ancestry cases, 172,873 European ancestry controls NA Affymetrix, Illumina [287541] 0 prostatitis http://www.ebi.ac.uk/efo/EFO_0003830 GCST90080620 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H36: diabetic eye disease (Gene-based burden) 970 European ancestry cases, 328,082 European ancestry controls NA Illumina [184145] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90081739 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse rate (UKB data field 4194) 173,103 European ancestry individuals NA Affymetrix, Illumina [287478] 2 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90079160 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Disc degeneration (Gene-based burden) 1,059 European ancestry cases, 330,695 European ancestry controls NA Illumina [184201] 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST90081907 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse wave reflection index (UKB data field 4195) 173,103 European ancestry individuals NA Affymetrix, Illumina [287478] 0 pulse wave reflection index measurement http://www.ebi.ac.uk/efo/EFO_0009804 GCST90079161 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51: disc degeneration (Gene-based burden) 938 European ancestry cases, 328,114 European ancestry controls NA Illumina [184145] 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST90081908 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse wave peak to peak time (UKB data field 4196) 173,016 European ancestry individuals NA Affymetrix, Illumina [287360] 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90079162 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diverticular disease diverticulitis (Gene-based burden) 5,370 European ancestry cases, 326,384 European ancestry controls NA Illumina [184201] 0 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90081849 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct left - abandon (UKB data field 4232) 2,642 European ancestry cases, 170,293 European ancestry controls NA Affymetrix, Illumina [287070] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90079165 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57: diverticular disease diverticulitis (Gene-based burden) 4,946 European ancestry cases, 324,106 European ancestry controls NA Illumina [184145] 0 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90081850 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct left - no (UKB data field 4232) 171,828 European ancestry cases, 1,107 European ancestry controls NA Affymetrix, Illumina [287070] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90079163 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Dry eyes (Gene-based burden) 1,085 European ancestry cases, 330,669 European ancestry controls NA Illumina [184201] 0 dry eye syndrome http://www.ebi.ac.uk/efo/EFO_1000906 GCST90081904 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct left (UKB data field 4232) 171,673 European ancestry cases, 1,262 European ancestry controls NA Affymetrix, Illumina [287070] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90079164 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04: dry eyes (Gene-based burden) 874 European ancestry cases, 328,178 European ancestry controls NA Illumina [184145] 0 dry eye syndrome http://www.ebi.ac.uk/efo/EFO_1000906 GCST90081905 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct right - abandon (UKB data field 4243) 2,680 European ancestry cases, 170,241 European ancestry controls NA Affymetrix, Illumina [287069] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90079168 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duodenal ulcer (Gene-based burden) 1,872 European ancestry cases, 329,882 European ancestry controls NA Illumina [184201] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90081847 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct right - no (UKB data field 4243) 171,830 European ancestry cases, 1,091 European ancestry controls NA Affymetrix, Illumina [287069] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90079166 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K26: Duodenal ulcer (Gene-based burden) 1,573 European ancestry cases, 327,479 European ancestry controls NA Illumina [184145] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90081848 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct right (UKB data field 4243) 171,634 European ancestry cases, 1,287 European ancestry controls NA Affymetrix, Illumina [287069] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90079167 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Dyspepsia indigestion (Gene-based burden) 836 European ancestry cases, 330,918 European ancestry controls NA Illumina [184201] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90081895 Exome-wide sequencing 2021-09-09 33891562 Hao Q 2021-04-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33891562 Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia. Acute lymphoblastic leukemia 466 Chinese ancestry cases, 1,466 Chinese ancestry controls NR NR [9466286] (imputed) 1 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST012357 Genome-wide genotyping array 2021-09-09 33891562 Hao Q 2021-04-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33891562 Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia. Acute lymphoblastic leukemia (childhood) 381 Chinese ancestry cases, 1,466 Chinese ancestry controls NR NR [9466286] (imputed) 1 childhood acute lymphoblastic leukemia http://purl.obolibrary.org/obo/MONDO_0000870 GCST012360 Genome-wide genotyping array 2021-09-09 33891562 Hao Q 2021-04-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33891562 Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia. Acute lymphoblastic leukemia (adult) 85 Chinese ancestry cases, 1,466 Chinese ancestry controls NR NR [9466286] (imputed) 1 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST012359 Genome-wide genotyping array 2021-09-09 33891562 Hao Q 2021-04-23 Aging (Albany NY) www.ncbi.nlm.nih.gov/pubmed/33891562 Age-related differences of genetic susceptibility to patients with acute lymphoblastic leukemia. Acute lymphoblastic leukemia (adult vs childhood) 85 Chinese ancestry adult cases, 381 Chinese ancestry childhood cases NR NR [9466286] (imputed) 1 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST012358 Genome-wide genotyping array 2021-09-10 33913524 Suzuki T 2021-04-29 Epilepsia www.ncbi.nlm.nih.gov/pubmed/33913524 Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24. Epilepsy 1,823 Japanese ancestry cases, 7,970 Japanese ancestry controls NR Illumina [9899436] (imputed) 7 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST012370 Genome-wide genotyping array 2021-10-20 33891350 Vann CG 2021-05-01 FASEB J www.ncbi.nlm.nih.gov/pubmed/33891350 An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men. Response to resistance training (vastus lateralis fiber area change) 109 men NR NR [315000] 2 muscle fiber cross-sectional area measurement, resistance training http://www.ebi.ac.uk/efo/EFO_0600036, http://www.ebi.ac.uk/efo/EFO_0600037 GCST012493 Genome-wide genotyping array 2021-10-20 33891350 Vann CG 2021-05-01 FASEB J www.ncbi.nlm.nih.gov/pubmed/33891350 An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training-induced muscle fiber hypertrophy in younger men. Response to resistance training (lean soft tissue mass change) 109 men NR NR [315000] 0 resistance training, lean body mass http://www.ebi.ac.uk/efo/EFO_0600037, http://www.ebi.ac.uk/efo/EFO_0004995 GCST012494 Genome-wide genotyping array 2021-05-18 33884653 Li C 2021-04-21 Mov Disord www.ncbi.nlm.nih.gov/pubmed/33884653 Genetic Modifiers of Age at Onset for Parkinson's Disease in Asians: A Genome-Wide Association Study. Parkinson's disease (age of onset) 3,456 Chinese ancestry individuals 1,490 Chinese ancestry individuals Illumina [~ 660000] (imputed) 2 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST011677 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 265) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013144 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 266) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013145 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 1) 19,670 European ancestry individuals NA NR [9705931] (imputed) 143 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012880 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 2) 19,670 European ancestry individuals NA NR [9705931] (imputed) 19 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012881 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 3) 19,670 European ancestry individuals NA NR [9705931] (imputed) 25 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012882 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 4) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012883 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 5) 19,670 European ancestry individuals NA NR [9705931] (imputed) 17 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012884 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 6) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012885 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 7) 19,670 European ancestry individuals NA NR [9705931] (imputed) 25 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012886 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 8) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012887 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 9) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012888 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 10) 19,670 European ancestry individuals NA NR [9705931] (imputed) 12 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012889 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 11) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012890 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 12) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012891 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 13) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012892 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 14) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012893 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 15) 19,670 European ancestry individuals NA NR [9705931] (imputed) 22 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012894 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 16) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012895 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 17) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012896 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 18) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012897 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 19) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012898 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 20) 19,670 European ancestry individuals NA NR [9705931] (imputed) 5 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012899 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 21) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012900 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 22) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012901 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 23) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012902 Genome-wide genotyping array 2021-10-07 33990960 Hong M 2021-05-14 Eur J Clin Invest www.ncbi.nlm.nih.gov/pubmed/33990960 Ethnic similarities in genetic polymorphisms associated with atrial fibrillation: Far East Asian vs European populations. Atrial fibrillation 9,118 East Asian ancestry cases, 33,467 East Asian ancestry controls NA NR [2286360] (imputed) 14 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST012460 Genome-wide genotyping array 2021-05-26 33093117 Yan Q 2020-10-22 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33093117 A genome-wide association study of severe asthma exacerbations in Latino children and adolescents. Severe exacerbations in childhood asthma 2,509 Latino cases, 1,501 Latino controls NA Affymetrix, Illumina [~ 6000000] (imputed) 2 asthma exacerbation measurement http://www.ebi.ac.uk/efo/EFO_0007614 GCST011737 Genome-wide genotyping array 2021-07-20 33080986 Furukawa K 2020-10-18 Nutrients www.ncbi.nlm.nih.gov/pubmed/33080986 A Genome-Wide Association Study Identifies the Association between the 12q24 Locus and Black Tea Consumption in Japanese Populations. Tea consumption 12,140 Japanese ancestry individuals 118 Japanese ancestry individuals Illumina [5256047] (imputed) 6 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST012044 Genome-wide genotyping array 2022-07-19 35148957 Toyoda Y 2022-01-31 Mol Genet Metab www.ncbi.nlm.nih.gov/pubmed/35148957 Genome-wide meta-analysis between renal overload type and renal underexcretion type of clinically defined gout in Japanese populations. Renal overload gout 486 renal overload-type gout male cases, 654 renal underexcretion-type gout male controls NA Illumina [7128846] (imputed) 3 renal overload-type gout http://www.ebi.ac.uk/efo/EFO_0021525 GCST90104597 Genome-wide genotyping array 2021-02-17 33356394 Gill D 2020-12-28 Hypertension www.ncbi.nlm.nih.gov/pubmed/33356394 Urate, Blood Pressure, and Cardiovascular Disease: Evidence From Mendelian Randomization and Meta-Analysis of Clinical Trials. Urate levels 454,183 European ancestry individuals NA NR [NR] 244 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST011119 Genome-wide genotyping array 2022-10-14 33093519 Trevino CE 2020-10-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33093519 Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Atrioventricular septal defects in Down syndrome 245 European ancestry cases, 242 European ancestry controls NA Affymetrix [2351951] (imputed) 0 Atrioventricular canal defect http://purl.obolibrary.org/obo/HP_0006695 GCST013023 Genome-wide genotyping array, Genome-wide sequencing 2022-10-14 33093519 Trevino CE 2020-10-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33093519 Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. Congenital heart malformation 3,000 European ancestry cases, 8,135 European ancestry controls NA Illumina [4684854] (imputed) 0 congenital heart malformation http://www.ebi.ac.uk/efo/EFO_0005269 GCST013022 Genome-wide genotyping array 2021-06-29 33093602 Chen IC 2020-10-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33093602 CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption. Excessive alcohol consumption 1,945 Taiwanese cases, 16,418 Taiwanese controls NA Affymetrix [6410722] (imputed) 3 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST011979 Genome-wide genotyping array 2021-06-29 33093602 Chen IC 2020-10-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33093602 CUX2, BRAP and ALDH2 are associated with metabolic traits in people with excessive alcohol consumption. Gamma glutamyl transferase levels 18,363 Taiwanese individuals NA Affymetrix [6410722] (imputed) 1 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST011978 Genome-wide genotyping array 2021-06-08 33941849 Chang X 2021-05-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33941849 Low frequency variants associated with leukocyte telomere length in the Singapore Chinese population. Telomere length 20,177 Chinese ancestry individuals 5,356 Chinese ancestry individuals Illumina [up to 4756872] (imputed) 4 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST011828 Genome-wide genotyping array 2021-05-10 31393333 Naramore SK 2019-11-01 J Pediatr Gastroenterol Nutr www.ncbi.nlm.nih.gov/pubmed/31393333 Serologic, but Not Genetic, Markers Are Associated With Impaired Anthropometrics at Diagnosis of Pediatric Crohn's Disease. Anthropometric traits in Crohn's disease (age at diagnosis) 637 European ancestry children, 46 African-American children, 29 Asian ancestry children, 60 children NA Illumina [121487] 0 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST011638 Targeted genotyping array [ImmunoChip] 2020-11-10 32600054 Qian H 2020-06-29 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32600054 Genome-Wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos. Estimated glomerular filtration rate 12,207 Hispanic/Latino individuals 8,224 African American individuals, 3,549 Hispanic individuals Illumina [32241096] (imputed) 1 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST010737 Genome-wide genotyping array 2020-11-10 32600054 Qian H 2020-06-29 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/32600054 Genome-Wide Association of Kidney Traits in Hispanics/Latinos Using Dense Imputed Whole-Genome Sequencing Data: The Hispanic Community Health Study/Study of Latinos. Urinary albumin-to-creatinine ratio 11,688 Hispanic/Latino individuals NA Illumina [32241096] (imputed) 13 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST010736 Genome-wide genotyping array 2023-07-25 31729158 Agopian AJ 2019-11-15 Am J Med Genet A www.ncbi.nlm.nih.gov/pubmed/31729158 X-chromosome association studies of congenital heart defects. Conotruncal heart defects (inherited effects) 720 trios NA Illumina [up to 155430] (imputed) 0 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST013177 Targeted genotyping array [X-chromosome] 2023-07-25 31729158 Agopian AJ 2019-11-15 Am J Med Genet A www.ncbi.nlm.nih.gov/pubmed/31729158 X-chromosome association studies of congenital heart defects. Left ventricular outflow tract obstructions 384 trios NA Illumina [up to 155430] (imputed) 0 Ventricular Outflow Obstruction http://www.ebi.ac.uk/efo/EFO_1001448 GCST013178 Targeted genotyping array [X-chromosome] 2023-07-25 31729158 Agopian AJ 2019-11-15 Am J Med Genet A www.ncbi.nlm.nih.gov/pubmed/31729158 X-chromosome association studies of congenital heart defects. Conotruncal heart defects 403 cases, 2,974 controls NA Illumina [114309] (imputed) 3 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST013176 Targeted genotyping array [X-chromosome] 2020-11-07 32996047 Alsubaie LM 2020-09-29 Mol Biol Rep www.ncbi.nlm.nih.gov/pubmed/32996047 Risk Y-haplotypes and pathogenic variants of Arab-ancestry boys with autism by an exome-wide association study. Autism 47 Saudi Arab ancestry young male cases, 43 Saudi Arab ancestry young male controls NA Illumina [243345] 9 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST010733 Exome genotyping array [Exome array] 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCAM1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089802 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCAM2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089466 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCF2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086205 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCF4 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087749 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCK1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088871 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCK2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087563 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCL 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087587 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCMAP 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087882 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCOA2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087739 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCR1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088926 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCR1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090153 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCR2 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088039 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCR3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088179 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NCR3LG1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089879 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDC80 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087190 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDE1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090811 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDNF 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089524 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDRG4 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089935 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDST1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089573 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDUFAF8 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090460 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDUFB11 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089803 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDUFB4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086403 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDUFB8 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090831 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDUFS4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086355 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NDUFV2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089804 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OPALIN 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089793 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OPCML 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088471 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OPHN1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087089 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OPRPN 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089480 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ORC6 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086951 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OSBPL11 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087286 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OSCAR 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089668 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OSCAR 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090268 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OSM 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087751 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OSM 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088021 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OSMR 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086488 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OSTN 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089770 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OTOF 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090522 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OTUB2 5,316 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087023 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OTUD5 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087015 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OXT 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090084 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OXT 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090149 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P2RX2 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090718 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P2RX6 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089752 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P3H1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089331 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P4HA1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086833 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P4HA2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086696 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P4HB 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086753 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P4HB 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088649 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein P4HTM 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086363 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ESRP1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090324 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ESRRA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090877 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ETHE1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 persulfide dioxygenase ETHE1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008258 GCST90088544 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ETNK1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090132 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ETS2 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086926 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ETV5 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087422 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EVA1B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090022 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EVA1C 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089616 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EVA1C 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090356 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EVI2B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087343 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EVL 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086840 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EVPL 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087718 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EWSR1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087331 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EXOSC1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089932 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EXOSC3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087097 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EXTL2 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089479 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EYS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090659 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EZR 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090800 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F10 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088225 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088791 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F11 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087924 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F13B 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089128 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087630 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088613 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089001 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NFKB1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090874 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NFU1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089821 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NGF 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089211 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NGFR 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090163 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NGFR 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090400 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NGRN 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089698 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NHEJ1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086698 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NHLRC3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090499 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NID1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088274 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NID2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088470 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NIP7 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087072 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NIPAL4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087278 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENO1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086541 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENO2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086231 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENO2 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086532 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENOX1 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087311 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENOX2 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087431 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENPP5 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089495 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENPP7 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088688 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENTPD1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088252 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENTPD1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089974 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENTPD3 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088689 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENTPD5 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088690 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENTPD6 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090390 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPB41 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088759 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPB41L1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087705 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPDR1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090466 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088381 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088903 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA10 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089263 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088781 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088382 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089720 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA5 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087773 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088520 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA7 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089725 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHA7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089726 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHB2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088904 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHB2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090061 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHB2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090144 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHB3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090561 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHB4 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088458 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHB6 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088905 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPHB6 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090591 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPO 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089215 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPOR 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088032 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPS15L1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088628 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EPYC 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090602 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EQTN 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086580 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERAP1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088830 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NXPH2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090728 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NXPH3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089269 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NXT1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090925 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OAF 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089411 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OAS1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086239 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OAZ1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090891 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OBP2A 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089477 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OBP2B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089143 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OCIAD1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088472 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OCRL 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086182 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ODC1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087611 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OIT3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089345 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLA1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087132 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLFM1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089157 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLFM2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090108 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLFM3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086386 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLFM3 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086565 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLFM4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088768 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLFML3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090253 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLFML3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090254 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLR1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088473 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OLR1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089908 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OMD 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089020 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OMD 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089171 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein OOSP2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089663 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088822 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein F5 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088802 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ID2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090689 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTN1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089546 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTN1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090447 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTN4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088319 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTNG1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089113 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTRK1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088408 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTRK2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088787 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTRK3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088008 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NTS 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089881 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUCB1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086276 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDC 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090352 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDC 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090360 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDCD3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088642 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDT12 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087676 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDT16L1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087025 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDT3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087233 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDT8 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089892 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUDT9 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090711 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUP210 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090838 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUP210L 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090776 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NUP98 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087217 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NXF1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086995 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein NXPH1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088743 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PA2G4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088643 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PABPC3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086273 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PABPC4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087095 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PABPN1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090382 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PACSIN1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087144 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PACSIN3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087902 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAEP 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090348 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAFAH1B2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088000 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAFAH1B3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086942 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAICS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090853 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAIP1 5,322 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086977 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAK3 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088354 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAK4 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087633 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAK5 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088355 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAK6 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088534 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PAM 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089098 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PANK3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087131 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAD51D 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087065 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAET1E 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089841 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAET1L 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086357 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAF1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086176 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAG1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086678 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RALA 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087869 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RAN 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 GTP-binding nuclear protein ran measurement http://www.ebi.ac.uk/efo/EFO_0020431 GCST90088651 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RANBP3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087733 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERAP2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090411 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERBB2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087982 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERBB3 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087983 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERBB4 5,322 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087984 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERCC1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087086 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERCC4 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090893 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EREG 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088823 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERH 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086821 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERLEC1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090408 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERLIN1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090290 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERMAP 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090242 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERMAP 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090818 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERN1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086625 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERO1A 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089638 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERO1B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089971 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERP27 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090636 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERP29 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087641 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERP29 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088843 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERP44 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089272 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ERVV-1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087050 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ESAM 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088164 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ESAM 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089869 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ESD 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088844 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ESM1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088519 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ESR1 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088141 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL4L1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088068 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 CCL5 measurement http://www.ebi.ac.uk/efo/EFO_0005117 GCST90087956 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL5 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CCL5 measurement http://www.ebi.ac.uk/efo/EFO_0005117 GCST90089053 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088794 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL8 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087658 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL8 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088070 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCM2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086924 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCNB1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089010 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCNB1;CDK1 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088378 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCNB1IP1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090786 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCNC 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089854 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCNH 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090860 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCPG1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090362 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCS 5,315 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087358 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCT5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087074 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCT7 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087601 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCT8 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087165 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD109 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 CD109 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008076 GCST90088292 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD14 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090416 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD163 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088882 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD164L2 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089565 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD177 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 10 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087384 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD1A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086456 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD1D 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090270 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089660 Genome-wide genotyping array 2021-05-05 33888516 Zheng T 2021-04-22 Gut www.ncbi.nlm.nih.gov/pubmed/33888516 Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease. Haemorrhoidal disease 218,920 European ancestry cases, 725,213 European ancestry controls NA Affymetrix, Illumina [8494288] (imputed) 102 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90014033 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAMK2A 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088333 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAMK2B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088334 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAMK2D 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088375 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAMKK1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088562 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAMP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090673 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAND1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087668 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CANT1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089454 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CANX 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090329 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086910 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAPG 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088833 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAPN1;CAPNS1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088011 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAPN2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087904 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAPN3 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086948 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAPSL 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087610 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAPZA1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086752 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CARD19 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089825 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CARD9 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086730 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CARHSP1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087241 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CARS 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087780 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CARTPT 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089188 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CASC4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086367 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CASC4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090331 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CASP10 5,324 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089006 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CASP2 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088800 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CASP3 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088448 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CASQ1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086646 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CASS4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087272 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAST 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088188 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAT 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088416 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAV2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090700 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAV3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090263 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBARP 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090523 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBFB 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086206 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBL 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086904 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBLN1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090623 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBLN4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089146 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBR1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086945 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBR3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087775 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBS 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086225 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBX5 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088725 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CBX7 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087342 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCBE1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086626 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCDC126 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089389 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCDC134 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089077 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCDC167 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089839 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCDC50 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086958 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCDC51 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087229 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCDC80 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088283 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCDC90B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089836 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089567 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA4 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087757 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA4 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088248 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA5A 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090300 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA6 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087657 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA6 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088335 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA7 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088336 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA8 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086724 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CA9 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088514 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CABLES2 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089662 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CABP7 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089661 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CACNA2D3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090359 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CACNB4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086557 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CACYBP 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086979 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CADM1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088318 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CADM3 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088469 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CADM4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090239 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CALB1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090908 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CALCA 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086301 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CALCOCO2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087053 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CALN1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086504 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CALR 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088989 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CALY 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086400 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CALY 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090385 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAMK1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088447 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CAMK1D 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088374 Genome-wide genotyping array 2021-01-22 33311586 Yonova-Doing E 2020-12-11 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33311586 Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract. Age-related nuclear cataracts 7,352 European ancestry individuals, 2,230 Chinese ancestry individuals, 2,369 Malay ancestry individuals, 2,200 Indian ancestry individuals 941 European ancestry cases, 922 European ancestry controls, 769 Chinese ancestry cases, 759 Chinese ancestry controls, 1,097 indian ancestry cases, 811 indian ancestry controls Illumina [8500000] (imputed) 8 Age-related nuclear cataract http://purl.obolibrary.org/obo/HP_0011142 GCST90013423 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087609 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088061 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL11 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 CCL11 measurement http://www.ebi.ac.uk/efo/EFO_0005188 GCST90088996 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL13 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CCL13 measurement http://www.ebi.ac.uk/efo/EFO_0009411 GCST90088601 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL14 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088127 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL15 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CCL15 measurement http://www.ebi.ac.uk/efo/EFO_0009413 GCST90087791 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL15 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CCL15 measurement http://www.ebi.ac.uk/efo/EFO_0009413 GCST90088428 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL16 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088809 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL17 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 8 CCL17 measurement http://www.ebi.ac.uk/efo/EFO_0009414 GCST90088432 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL18 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088203 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL19 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CCL19 measurement http://www.ebi.ac.uk/efo/EFO_0009415 GCST90088816 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004749 GCST90087965 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL20 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 CCL20 measurement http://www.ebi.ac.uk/efo/EFO_0010766 GCST90087946 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL21 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CCL21 measurement http://www.ebi.ac.uk/efo/EFO_0009416 GCST90087955 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL22 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088427 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL23 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 CCL23 measurement http://www.ebi.ac.uk/efo/EFO_0009417 GCST90088130 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL23 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CCL23 measurement http://www.ebi.ac.uk/efo/EFO_0009417 GCST90088189 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL24 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 CCL24 measurement http://www.ebi.ac.uk/efo/EFO_0009418 GCST90088586 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL25 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CCL25 measurement http://www.ebi.ac.uk/efo/EFO_0010768 GCST90087756 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL25 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 CCL25 measurement http://www.ebi.ac.uk/efo/EFO_0010768 GCST90088027 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL26 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090528 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL27 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087925 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL28 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 CCL28 measurement http://www.ebi.ac.uk/efo/EFO_0010769 GCST90088125 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CCL3 measurement http://www.ebi.ac.uk/efo/EFO_0010770 GCST90088199 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CCL3L3 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088069 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL13 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 13 measurement http://www.ebi.ac.uk/efo/EFO_0008171 GCST90088222 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL13RA1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-13 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020493 GCST90087993 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL15 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086450 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL15RA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 interleukin 15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008172 GCST90087746 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL15RA 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin 15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008172 GCST90088390 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL16 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin 16 measurement http://www.ebi.ac.uk/efo/EFO_0008173 GCST90088064 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90087632 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17A 5,327 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90088421 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17A 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90090530 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17B 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90087720 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17B 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90088422 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17C 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90090586 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17D 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90088594 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17F 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90087724 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17F 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST90088065 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17RA 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90088172 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17RB 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin 17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0008176 GCST90088908 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17RB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0008176 GCST90089327 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17RC 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-17 receptor c measurement http://www.ebi.ac.uk/efo/EFO_0020494 GCST90089048 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL17RD 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin 17 receptor D measurement http://www.ebi.ac.uk/efo/EFO_0008177 GCST90088350 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL18 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST90089131 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL18BP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-18-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020495 GCST90088223 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL18R1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90087765 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL18R1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90088391 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL18RAP 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 7 interleukin 18 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008179 GCST90086281 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL18RAP 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 18 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008179 GCST90088173 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL19 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008192 GCST90088196 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1A 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST90088784 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088197 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1R1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90088171 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1R2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087809 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1R2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089134 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1RAP 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087741 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1RAP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087990 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1RAPL2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088907 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1RL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088634 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1RL2 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088174 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL1RN 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089015 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 2 measurement http://www.ebi.ac.uk/efo/EFO_0008331 GCST90088221 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL20 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-20 measurement http://www.ebi.ac.uk/efo/EFO_0020496 GCST90088596 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL20RA 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-20 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020497 GCST90088909 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL20RB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087441 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL21 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089674 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL21R 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090660 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL22 5,331 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90087653 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL22 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90088066 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL22RA1 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90088462 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL22RA1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90090774 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL22RA2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90088910 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL22RA2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90090699 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL23R 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin 23 receptor measurement http://www.ebi.ac.uk/efo/EFO_0008181 GCST90088911 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL24 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-24 measurement http://www.ebi.ac.uk/efo/EFO_0020502 GCST90088313 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL25 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 25 measurement http://www.ebi.ac.uk/efo/EFO_0008182 GCST90088595 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL27RA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin 27 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008183 GCST90088948 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL2RA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0010587 GCST90088237 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL2RB 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090643 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL2RG 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087994 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL3 5,323 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020503 GCST90088763 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL31 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086280 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL31RA 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090097 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL32 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089744 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL32 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090473 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL33 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087298 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL34 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088738 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL36A 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086503 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL36A 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087820 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL36B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087819 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL36G 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090519 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL37 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088034 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL3RA 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90087655 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL3RA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90088713 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL4 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 4 measurement http://www.ebi.ac.uk/efo/EFO_0008184 GCST90087593 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL4 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 4 measurement http://www.ebi.ac.uk/efo/EFO_0008184 GCST90088128 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL4R 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088211 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL5 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 5 measurement http://www.ebi.ac.uk/efo/EFO_0008185 GCST90086530 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD34 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090455 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD36 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088158 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD38 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086771 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD38 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086774 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD38 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089707 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD3E 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090028 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD3G 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089927 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD4 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088235 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD40 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CD40 measurement http://www.ebi.ac.uk/efo/EFO_0010586 GCST90090256 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD40 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 CD40 measurement http://www.ebi.ac.uk/efo/EFO_0010586 GCST90090651 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD40LG 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088436 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD44 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090606 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD47 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089543 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD47 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089549 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD48 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088294 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12A;IL12B 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086246 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12A;IL12B 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087945 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12A;IL12B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086245 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 obsolete_interleukin-12 subunit B measurement http://www.ebi.ac.uk/efo/EFO_0010787 GCST90087646 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12B;IL23A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086243 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12B;IL23A 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088716 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12RB1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90087623 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12RB1 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90087992 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL12RB2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin-12 receptor subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020492 GCST90088527 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL13 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 interleukin 13 measurement http://www.ebi.ac.uk/efo/EFO_0008171 GCST90087770 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD200 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088934 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD200R1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086381 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD200R1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088925 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD200R1 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090671 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD200R1L 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090425 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD207 5,327 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088341 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD209 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90088190 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD22 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 B-cell receptor CD22 measurement http://www.ebi.ac.uk/efo/EFO_0020171 GCST90088126 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD226 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088894 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD226 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089167 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD244 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CD244 measurement http://www.ebi.ac.uk/efo/EFO_0010772 GCST90088895 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD247 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089756 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD27 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 CD27 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008078 GCST90089031 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD274 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088892 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD276 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087303 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300A 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089106 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300C 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087424 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300C 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088897 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300E 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086451 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300E 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090104 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300LB 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086418 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300LF 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089100 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD300LG 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090903 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD33 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088239 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD34 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086663 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein IL5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 interleukin 5 measurement http://www.ebi.ac.uk/efo/EFO_0008185 GCST90088504 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CD5 measurement http://www.ebi.ac.uk/efo/EFO_0010773 GCST90087753 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CD5 measurement http://www.ebi.ac.uk/efo/EFO_0010773 GCST90089081 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD55 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088899 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD58 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086505 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD59 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086295 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD59 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086775 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD5L 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088295 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD63 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090545 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD7 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086901 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD70 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089213 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD70 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090280 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD72 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089617 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD72 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089618 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD74 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089601 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD74 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090269 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD79A 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089838 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD79B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089357 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD80 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087639 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD80 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087974 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD83 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088896 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD84 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088475 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD84 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090032 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD84 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090286 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CD86 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089004 Genome-wide genotyping array 2020-09-28 30535219 Choi SH 2018-12-01 JAMA www.ncbi.nlm.nih.gov/pubmed/30535219 Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation. Early onset atrial fibrillation 2,781 European ancestry cases, 4,959 European ancestry controls NA NR [8248975] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST010636 Genome-wide sequencing 2021-07-27 33385171 Hagg S 2020-12-31 Hum Genet www.ncbi.nlm.nih.gov/pubmed/33385171 Deciphering the genetic and epidemiological landscape of mitochondrial DNA abundance. Mitochondrial DNA levels 295,150 European ancestry individuals NA Affymetrix [3505788] (imputed) 66 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST012072 Genome-wide genotyping array 2020-10-01 32949544 Jones E 2020-09-16 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/32949544 Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study. Creutzfeldt-Jakob disease (sporadic) 4,110 European ancestry cases, 13,569 European ancestry controls 1,098 European ancestry cases, 498 ,016 European ancestry controls Affymetrix, Illumina [6314492] (imputed) 4 sporadic Creutzfeld Jacob disease http://www.ebi.ac.uk/efo/EFO_1000656 GCST90001389 Genome-wide genotyping array 2021-04-21 31748686 Oh JJ 2019-11-20 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31748686 An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer. Prostate cancer 985 Korean ancestry cases and 6,273 Korean ancestry controls NA Illumina [71270] 2 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011535 Exome genotyping array [Exome array] 2021-01-22 33097703 Surakka I 2020-10-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33097703 MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk. Ultradistal forearm bone mineral density 21,907 European ancestry individuals NA Illumina [11603265] (imputed) 32 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90013422 Genome-wide genotyping array, Genome-wide sequencing 2021-11-15 34309184 Kawaratani H 2021-07-26 Liver Int www.ncbi.nlm.nih.gov/pubmed/34309184 A Genome-Wide Association Study Identifying SVEP1 Variant as a Predictor of Response to Tolvaptan for Cirrhotic Ascites. Response to tolvaptan in hepatic ascites (body weight gain) 25 Japanese ancestry non-responder cases with increase of body weight, 156 Japanese ancestry responder controls with >1.5 kg decrease of body weight 55 Japanese ancestry non-responder cases with increase of body weight, 177 Japanese ancestry responder controls with >1.5 kg decrease of body weight Affymetrix [5420892] (imputed) 3 response to tolvaptan, body weight gain http://www.ebi.ac.uk/efo/EFO_0600065, http://www.ebi.ac.uk/efo/EFO_0004566 GCST90027078 Genome-wide genotyping array 2021-11-26 34336000 Li L 2021-07-14 Behav Neurol www.ncbi.nlm.nih.gov/pubmed/34336000 Use of Deep-Learning Genomics to Discriminate Healthy Individuals from Those with Alzheimer's Disease or Mild Cognitive Impairment. Alzheimer's disease 622 cases, 366 controls NA Illumina [NR] 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90026487 Genome-wide genotyping array 2021-07-07 33382404 Sallinen RJ 2020-12-31 J Nutr www.ncbi.nlm.nih.gov/pubmed/33382404 Genetic Risk Score for Serum 25-Hydroxyvitamin D Concentration Helps to Guide Personalized Vitamin D Supplementation in Healthy Finnish Adults. Serum 25-Hydroxyvitamin D levels 3,399 Finnish ancestry individuals NA Illumina [~ 7700000] (imputed) 2 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST012014 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract (Gene-based burden) 8,629 European ancestry cases, 323,125 European ancestry controls NA Illumina [184201] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90081742 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Extremely unhappy (UKB data field 4559) 985 European ancestry cases, 175,103 European ancestry controls NA Affymetrix, Illumina [291128] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90079199 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26: cataract (Gene-based burden) 7,792 European ancestry cases, 321,260 European ancestry controls NA Illumina [184145] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90081743 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Moderately happy (UKB data field 4559) 51,919 European ancestry cases, 124,169 European ancestry controls NA Affymetrix, Illumina [291128] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90079196 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cervical spondylosis (Gene-based burden) 3,241 European ancestry cases, 328,513 European ancestry controls NA Illumina [184201] 0 cervical spondylosis http://www.ebi.ac.uk/efo/EFO_0009610 GCST90081877 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Moderately unhappy (UKB data field 4559) 8,490 European ancestry cases, 167,598 European ancestry controls NA Affymetrix, Illumina [291128] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90079197 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47: cervical spondylosis (Gene-based burden) 2,805 European ancestry cases, 326,247 European ancestry controls NA Illumina [184145] 0 cervical spondylosis http://www.ebi.ac.uk/efo/EFO_0009610 GCST90081878 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Very happy (UKB data field 4559) 84,228 European ancestry cases, 91,860 European ancestry controls NA Affymetrix, Illumina [291128] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90079195 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chickenpox (Gene-based burden) 7,564 European ancestry cases, 324,190 European ancestry controls NA Illumina [184201] 0 chickenpox http://www.ebi.ac.uk/efo/EFO_0007204 GCST90081933 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Very unhappy (UKB data field 4559) 2,347 European ancestry cases, 173,741 European ancestry controls NA Affymetrix, Illumina [291128] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90079198 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B01: chickenpox (Gene-based burden) 6,575 European ancestry cases, 322,477 European ancestry controls NA Illumina [184145] 0 chickenpox http://www.ebi.ac.uk/efo/EFO_0007204 GCST90081934 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - final answer - Grey cross (UKB data field 4293) 3,159 European ancestry cases, 172,724 European ancestry controls NA Affymetrix, Illumina [290993] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90079173 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80: cholelithiasis or gall stones (Gene-based burden) 7,669 European ancestry cases, 324,085 European ancestry controls NA Illumina [184201] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90081690 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - final answer - Orange circle (UKB data field 4293) 169,042 European ancestry cases, 6,841 European ancestry controls NA Affymetrix, Illumina [290993] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90079174 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80: cholelithiasis or gall stones (Gene-based burden) 7,073 European ancestry cases, 321,979 European ancestry controls NA Illumina [184145] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90081691 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - final answer - Pink star (UKB data field 4293) 4,530 European ancestry cases, 171,353 European ancestry controls NA Affymetrix, Illumina [290993] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90079172 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic fatigue syndrome (Gene-based burden) 2,009 European ancestry cases, 329,745 European ancestry controls NA Illumina [184201] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90081881 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Extremely happy (UKB data field 4570) 25,041 European ancestry cases, 150,736 European ancestry controls NA Affymetrix, Illumina [290804] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90079200 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R5382: chronic fatigue syndrome (Gene-based burden) 1,753 European ancestry cases, 327,298 European ancestry controls NA Illumina [184145] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90081882 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Moderately happy (UKB data field 4570) 57,135 European ancestry cases, 118,642 European ancestry controls NA Affymetrix, Illumina [290804] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90079202 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive airways disease copd (Gene-based burden) 1,758 European ancestry cases, 329,996 European ancestry controls NA Illumina [184201] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90081659 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Moderately unhappy (UKB data field 4570) 4,889 European ancestry cases, 170,888 European ancestry controls NA Affymetrix, Illumina [290804] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90079203 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44: chronic obstructive airways disease copd (Gene-based burden) 1,651 European ancestry cases, 327,401 European ancestry controls NA Illumina [184145] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90081660 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Very happy (UKB data field 4570) 96,044 European ancestry cases, 79,733 European ancestry controls NA Affymetrix, Illumina [290804] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90079201 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic sinusitis (Gene-based burden) 3,481 European ancestry cases, 328,273 European ancestry controls NA Illumina [184201] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90081822 Exome-wide sequencing 2021-09-09 33937227 Zhang W 2021-04-16 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33937227 Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft. Orofacial cleft x maternal periconceptional smoking interaction (1df) 321 European ancestry exposed trios, 875 European ancestry unexposed trios, 42 Asian ancestry exposed trios, 1,224 Asian ancestry unexposed trios, 79 Latin American exposed trios, 434 Latin American unexposed trios NA Illumina [up to 6762077] (imputed) 2 smoking status measurement, Orofacial cleft http://www.ebi.ac.uk/efo/EFO_0006527, http://purl.obolibrary.org/obo/HP_0000202 GCST012367 Genome-wide genotyping array 2021-09-09 33937227 Zhang W 2021-04-16 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33937227 Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft. Orofacial cleft x maternal periconceptional alcohol use interaction (1df) 419 European ancestry exposed trios, 681 European ancestry unexposed trios, 40 Asian ancestry exposed trios, 1,213 Asian ancestry unexposed trios, 103 Latin American exposed trios, 407 Latin American unexposed trios NA Illumina [up to 6762077] (imputed) 1 Orofacial cleft, alcohol consumption measurement http://purl.obolibrary.org/obo/HP_0000202, http://www.ebi.ac.uk/efo/EFO_0007878 GCST012366 Genome-wide genotyping array 2021-09-09 33937227 Zhang W 2021-04-16 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33937227 Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft. Orofacial cleft x maternal periconceptional multivitamin use interaction (1df) 661 European ancestry exposed trios, 328 European ancestry unexposed trios, 293 Asian ancestry exposed trios, 805 Asian ancestry unexposed trios, 260 Latin American exposed trios, 140 Latin American unexposed trios NA Illumina [up to 6762077] (imputed) 3 Orofacial cleft, vitamin supplement exposure measurement http://purl.obolibrary.org/obo/HP_0000202, http://www.ebi.ac.uk/efo/EFO_0009116 GCST012365 Genome-wide genotyping array 2021-09-09 33937227 Zhang W 2021-04-16 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33937227 Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft. Orofacial cleft x maternal periconceptional smoking interaction (2df) 321 European ancestry exposed trios, 875 European ancestry unexposed trios, 42 Asian ancestry exposed trios, 1,224 Asian ancestry unexposed trios, 79 Latin American exposed trios, 434 Latin American unexposed trios NA Illumina [up to 6762077] (imputed) 1 smoking status measurement, Orofacial cleft http://www.ebi.ac.uk/efo/EFO_0006527, http://purl.obolibrary.org/obo/HP_0000202 GCST012364 Genome-wide genotyping array 2021-09-09 33937227 Zhang W 2021-04-16 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33937227 Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft. Orofacial cleft x maternal periconceptional alcohol use interaction (2df) 419 European ancestry exposed trios, 681 European ancestry unexposed trios, 40 Asian ancestry exposed trios, 1,213 Asian ancestry unexposed trios, 103 Latin American exposed trios, 407 Latin American unexposed trios NA Illumina [up to 6762077] (imputed) 1 Orofacial cleft, alcohol consumption measurement http://purl.obolibrary.org/obo/HP_0000202, http://www.ebi.ac.uk/efo/EFO_0007878 GCST012363 Genome-wide genotyping array 2021-09-09 33937227 Zhang W 2021-04-16 Front Cell Dev Biol www.ncbi.nlm.nih.gov/pubmed/33937227 Detecting Gene-Environment Interaction for Maternal Exposures Using Case-Parent Trios Ascertained Through a Case With Non-Syndromic Orofacial Cleft. Orofacial cleft x maternal periconceptional multivitamin use interaction (2df) 661 European ancestry exposed trios, 328 European ancestry unexposed trios, 293 Asian ancestry exposed trios, 805 Asian ancestry unexposed trios, 260 Latin American exposed trios, 140 Latin American unexposed trios NA Illumina [up to 6762077] (imputed) 2 Orofacial cleft, vitamin supplement exposure measurement http://purl.obolibrary.org/obo/HP_0000202, http://www.ebi.ac.uk/efo/EFO_0009116 GCST012362 Genome-wide genotyping array 2021-06-11 33941608 Khan A 2021-05-03 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/33941608 Medical Records-Based Genetic Studies of the Complement System. Complement C3 levels 3,210 European ancestry individuals, 589 African ancestry individuals, 150 East Asian ancestry individuals NA NR [NR] (imputed) 4 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST011834 Genome-wide genotyping array 2021-06-11 33941608 Khan A 2021-05-03 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/33941608 Medical Records-Based Genetic Studies of the Complement System. Complement C4 levels 3,247 European ancestry individuals, 600 African ancestry individuals, 151 East Asian ancestry individuals NA NR [NR] (imputed) 14 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST011833 Genome-wide genotyping array 2021-05-05 31511581 Joo J 2019-09-11 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31511581 The association of integration patterns of human papilloma virus and single nucleotide polymorphisms on immune- or DNA repair-related genes in cervical cancer patients. Human papilloma virus infection in cervical cancer 161 Korean ancestry individuals with cervical cancer NA Affymetrix [166505] 0 human papilloma virus infection http://www.ebi.ac.uk/efo/EFO_0001668 GCST011620 Targeted genotyping array [custom array] 2021-05-13 31622379 Best LG 2019-10-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/31622379 Genetic analysis of hsCRP in American Indians: The Strong Heart Family Study. C-reactive protein levels 1,892 American Indian ancestry individuals NA Illumina [120972] 3 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011657 Targeted genotyping array [Cardio-MetaboChip] 2021-06-03 33926923 Rahman MS 2021-04-29 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33926923 Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain. Chronic widespread musculoskeletal pain 6,914 European ancestry cases, 242,929 European ancestry controls 14,177 European ancestry cases, 28,903 European ancestry controls Affymetrix [NR] (imputed) 0 chronic widespread pain http://www.ebi.ac.uk/efo/EFO_0010099 GCST011779 Genome-wide genotyping array 2021-09-08 33859377 Thorp JG 2021-04-15 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33859377 Symptom-level modelling unravels the shared genetic architecture of anxiety and depression. Depression at least 5,919 European ancestry cases, at least 130,691 European ancestry controls 634,037 European ancestry cases, 1,308,690 European ancestry controls NR [9417325] (imputed) 47 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST012355 Genome-wide genotyping array 2021-09-08 33859377 Thorp JG 2021-04-15 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33859377 Symptom-level modelling unravels the shared genetic architecture of anxiety and depression. Anxiety at least 23,606 European ancestry cases, at least 113,351 European ancestry controls 624,615 European ancestry cases, 1,310,854 European ancestry controls NR [9417325] (imputed) 55 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST012354 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 24) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012903 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 25) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012904 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 26) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012905 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 27) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012906 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 28) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012907 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 29) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012908 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 30) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012909 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 31) 19,670 European ancestry individuals NA NR [9705931] (imputed) 7 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012910 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 32) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012911 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 33) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012912 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 34) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012913 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 35) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012914 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 36) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012915 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 37) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012916 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 38) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012917 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 39) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012918 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 40) 19,670 European ancestry individuals NA NR [9705931] (imputed) 7 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012919 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 41) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012920 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 42) 19,670 European ancestry individuals NA NR [9705931] (imputed) 5 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012921 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 43) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012922 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 44) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012923 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 45) 19,670 European ancestry individuals NA NR [9705931] (imputed) 5 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012924 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 46) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012925 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 47) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012926 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 48) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012927 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 74) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012953 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 75) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012954 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 76) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012955 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 77) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012956 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 78) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012957 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 79) 19,670 European ancestry individuals NA NR [9705931] (imputed) 4 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012958 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 80) 19,670 European ancestry individuals NA NR [9705931] (imputed) 4 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012959 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 81) 19,670 European ancestry individuals NA NR [9705931] (imputed) 3 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012960 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 82) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012961 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 83) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012962 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 84) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012963 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 85) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012964 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 86) 19,670 European ancestry individuals NA NR [9705931] (imputed) 8 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012965 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 87) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012966 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 88) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012967 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 89) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012968 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 267) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013146 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 268) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013147 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 269) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013148 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 270) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013149 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 271) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013150 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 272) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013151 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 273) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013152 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 274) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013153 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 275) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013154 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 49) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012928 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 50) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012929 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 51) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012930 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 52) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012931 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 53) 19,670 European ancestry individuals NA NR [9705931] (imputed) 4 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012932 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 54) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012933 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 55) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012934 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 56) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012935 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 57) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012936 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 58) 19,670 European ancestry individuals NA NR [9705931] (imputed) 4 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012937 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 59) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012938 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 60) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012939 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 61) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012940 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 62) 19,670 European ancestry individuals NA NR [9705931] (imputed) 6 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012941 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 63) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012942 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 64) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012943 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 65) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012944 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 66) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012945 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 67) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012946 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 68) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012947 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 69) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012948 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 70) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012949 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 71) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012950 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 72) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012951 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 73) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90012952 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 240) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013119 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 241) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013120 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 242) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013121 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 243) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013122 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 244) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013123 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 245) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013124 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 246) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013125 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 247) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013126 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 248) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013127 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 249) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013128 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 250) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013129 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 251) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013130 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 252) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013131 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 253) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013132 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 254) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013133 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 255) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013134 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 256) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013135 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 257) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013136 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 258) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013137 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 259) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013138 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 260) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013139 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 261) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013140 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 262) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013141 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 263) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013142 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 264) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013143 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 276) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013155 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 277) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013156 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 278) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013157 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 279) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013158 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 280) 19,670 European ancestry individuals NA NR [9705931] (imputed) 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013159 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 281) 19,670 European ancestry individuals NA NR [9705931] (imputed) 4 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013160 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 282) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013161 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 283) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013162 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 284) 19,670 European ancestry individuals NA NR [9705931] (imputed) 0 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013163 Genome-wide genotyping array 2022-03-28 33821002 Naqvi S 2021-04-05 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33821002 Shared heritability of human face and brain shape. Brain shape (segment 285) 19,670 European ancestry individuals NA NR [9705931] (imputed) 1 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90013164 Genome-wide genotyping array 2021-10-22 34413389 Ruggiero D 2021-08-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34413389 Genetics of PlGF plasma levels highlights a role of its receptors and supports the link between angiogenesis and immunity. Placenta growth factor levels 1,600 European ancestry individuals 468 European ancestry individuals Illumina [8281256] (imputed) 5 placenta growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010626 GCST90029072 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APLP2 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089918 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APMAP 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086361 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOA1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088048 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOA2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089676 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOA5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086682 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOA5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087302 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOA5 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090482 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOB 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90088077 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOBEC3G 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087662 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOC2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089356 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOC3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089441 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOD 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90088762 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOD 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90090089 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOE 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90087936 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOE 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90088135 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein A1CF 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086971 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein A2M 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 alpha-2-macroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020138 GCST90088491 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein A4GALT 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090277 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein A4GNT 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086468 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AAGAB 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086887 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AARS 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086920 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABCC6 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090392 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABHD12 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089860 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABHD14A 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089163 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABL1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase ABL1 measurement http://www.ebi.ac.uk/efo/EFO_0020818 GCST90088326 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTS5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90088240 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTS6 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089427 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTSL1 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089506 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTSL2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089381 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADCYAP1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088751 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADCYAP1 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088752 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADCYAP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090102 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADCYAP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090198 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADCYAP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090200 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADGRE2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088731 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADGRE5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088085 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADGRF1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086633 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADGRF5 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089406 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADGRG2 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086444 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADGRG5 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088736 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADH1B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090846 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADH4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090129 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADH5 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086711 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADH7 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086716 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADI1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086999 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADIPOQ 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088439 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADM 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087796 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADM 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089925 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADM 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090222 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADM2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090052 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABL2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088327 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABL2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088987 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABLIM3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087540 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ABO 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090584 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACACB 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087299 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACAD8 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086731 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACAN 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088286 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACAP2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086922 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACBD6 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086218 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACBD7 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087528 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACE 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 angiotensin-converting enzyme measurement http://www.ebi.ac.uk/efo/EFO_0006515 GCST90086419 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACE2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088078 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACHE 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086526 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACLY 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087166 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACOT7 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090349 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACP1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088550 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACP2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090573 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACP5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088282 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACP6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089187 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACP7 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089984 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACRV1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086312 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACTN1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090855 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACTN2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090856 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACVR1B 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088079 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACVR2B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090687 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AIFM1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087433 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AIFM1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090733 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AIMP1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088031 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AIP 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088541 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AK1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088869 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AK2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086710 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AK5 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087561 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKR1A1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088624 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKR1B1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090865 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKR1C1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087101 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKR7A2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088623 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKT1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088114 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKT2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087905 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKT2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089022 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AKT3 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088359 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALB 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90088490 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALCAM 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089037 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALDH1A1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086648 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALDH1A3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090847 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALDH3A1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086764 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALDH3B1 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087315 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALDOA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089226 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALDOC 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090880 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALK 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090078 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALKBH5 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090301 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALOX15B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086970 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALPI 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086285 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALPL 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088075 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALPPL2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089550 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALPPL2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089552 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ALPPL2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089851 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMBN 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089475 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMELX 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090231 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMH 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088817 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMHR2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088891 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMIGO1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090944 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMIGO2 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087810 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMIGO2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089564 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMN 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088662 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMY1A 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089921 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AMY2B 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086269 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANAPC10 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086923 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANAPC7 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086856 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANG 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088789 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPT1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088081 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPT2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087591 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPT2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087973 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPT4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087950 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086564 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL1 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090503 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACVRL1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088155 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACY1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088328 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ACYP2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087243 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM10 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090189 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM10 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090251 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM11 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089514 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM12 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088683 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM15 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090933 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM17 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090358 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM17 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090410 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM19 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090244 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM19 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090399 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM22 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089934 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM23 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089632 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM29 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087521 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM30 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090223 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM32 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089862 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM7 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086437 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAM9 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088511 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMDEC1 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090517 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTS1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088246 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTS13 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 ADAMTS13 measurement http://www.ebi.ac.uk/efo/EFO_0009269 GCST90088247 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTS15 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088722 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTS3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090337 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADAMTS4 5,320 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088080 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HPX 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087760 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HPX 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088060 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HRASLS2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089857 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HRC 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089513 Genome-wide genotyping array 2022-06-07 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HRG 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088856 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HRK 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089982 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HS3ST1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089346 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HS3ST3A1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090093 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HS3ST3B1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089604 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HS3ST4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090437 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HS3ST5 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086426 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HS6ST1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089046 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HS6ST2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087504 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSD17B1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088761 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSD17B10 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088629 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSD17B14 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087689 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSD17B2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090424 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSD17B7 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090096 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSD17B7 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090915 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSF1 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086823 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSP90AA1;HSP90AB1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087988 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSP90AA1;HSP90AB1 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087989 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSP90AB1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089047 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSP90B1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089394 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HSPA1A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088582 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADPGK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089302 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADRM1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090477 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADSL 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088879 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADSS 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087120 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ADSSL1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087708 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AFAP1L1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090889 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AFM 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088767 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AFP 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089209 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGA 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086267 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGAP2 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087859 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGAP3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087683 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGER 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088583 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGFG1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086853 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGGF1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090014 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGO1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086837 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGR2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088825 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGR3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089136 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGRP 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088082 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AGT 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088412 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AHCYL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087126 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AHSA1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086828 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AHSG 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086518 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AHSG 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088441 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AHSP 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090456 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AIF1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088104 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086249 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086252 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL3 5,327 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088287 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL4 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088512 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089374 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANGPTL8 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089714 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANK2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089775 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANKRD1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086254 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANKRD27 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086988 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANKRD46 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089876 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANOS1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089523 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANP32A 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087359 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANP32B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088625 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANTXR1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086286 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088826 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA10 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087557 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ANXA2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087620 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMBS 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086777 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMG20A 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087177 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMG20B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086793 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMGB1 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087957 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMGB2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089563 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMGB3 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087219 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMGCR 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088968 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein HMGCS1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087481 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087369 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090195 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089208 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090206 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSRP1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090472 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RTBDN 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090238 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RTF1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089797 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RTN4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088939 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RTN4R 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088927 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RUFY1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086737 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RUNX3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086561 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RUVBL1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086935 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RXFP1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087811 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RYK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089074 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A11 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087715 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A12 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089222 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A13 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089746 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOE 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90088136 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOH 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090105 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOL1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086772 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086773 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090724 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOM 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086272 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOM 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087803 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APOO 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090665 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATG4B 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087572 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATG5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087093 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATG7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087109 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP13A1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087590 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP1A1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086899 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP1B1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087417 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATP1B2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089742 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCER2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088293 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCGR1A 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088306 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCGR2A 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088303 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCGR2B 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088304 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCGR3B 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088305 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCMR 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089505 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCN1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088459 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCN2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087631 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCN2 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088307 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCN3 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087763 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCN3 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089043 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089174 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089944 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090039 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088691 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090419 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090432 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL5 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089282 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF6 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020383 GCST90088588 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90087728 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF7 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90088712 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF8 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor basic measurement http://www.ebi.ac.uk/efo/EFO_0008130 GCST90087921 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF8 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor basic measurement http://www.ebi.ac.uk/efo/EFO_0008130 GCST90087942 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF8 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor basic measurement http://www.ebi.ac.uk/efo/EFO_0008130 GCST90088677 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF9 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020387 GCST90088058 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFBP1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090725 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFBP3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086618 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFR1 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020388 GCST90089070 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFR2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020389 GCST90088522 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFR3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90087597 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFR3 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90088523 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFR4 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020391 GCST90088848 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFRL1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089283 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGFRL1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089314 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGG 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088849 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGL1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089073 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGR 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase FGR measurement http://www.ebi.ac.uk/efo/EFO_0020822 GCST90088524 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FH 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90087412 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FHIT 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 histidine triad nucleotide-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020450 GCST90090840 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FIBCD1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090668 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FIG4 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089587 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FJX1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089924 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FKBP14 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090641 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FCRL6 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089530 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FDX1L 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086627 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FEN1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087081 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FER 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088630 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FERMT3 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087094 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FETUB 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088347 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FEV 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 FEV change measurement http://www.ebi.ac.uk/efo/EFO_0005921 GCST90087197 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGA;FGB;FGG 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088076 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGA;FGB;FGG 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088803 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF1 5,323 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020375 GCST90088414 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF10 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 fibroblast growth factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020376 GCST90087941 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF12 5,336 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 12 measurement http://www.ebi.ac.uk/efo/EFO_0020377 GCST90088675 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF16 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90087638 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF16 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90088676 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF17 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 17 measurement http://www.ebi.ac.uk/efo/EFO_0020379 GCST90088418 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF18 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 18 measurement http://www.ebi.ac.uk/efo/EFO_0020380 GCST90088055 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF19 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90087637 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF19 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90088056 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008129 GCST90088187 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF20 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 20 measurement http://www.ebi.ac.uk/efo/EFO_0020381 GCST90088057 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF22 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor basic measurement http://www.ebi.ac.uk/efo/EFO_0008130 GCST90090730 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF23 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90088521 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor basic measurement http://www.ebi.ac.uk/efo/EFO_0008130 GCST90089909 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF4 5,328 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020382 GCST90088581 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FGF5 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90088217 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ART3 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089959 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ART4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089507 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARTN 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088137 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASAH1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089193 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASAH2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088273 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASAP2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087501 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASCC1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086388 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASGR1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089038 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASGR2 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090708 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASH1L 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087105 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASH2L 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087257 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASIC4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089588 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASIP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089140 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASL 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086631 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASMTL 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086228 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASNA1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087565 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASPH 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089611 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASPN 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089434 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASPRV1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086493 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASPRV1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087340 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ASTL 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089970 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATAD1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089535 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATAD2 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087348 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATF6 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086655 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ATF6B 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086722 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FKBP1B 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086803 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FKBP2 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090640 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FKBP6 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087048 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FKBP7 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090609 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLII 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087145 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLNA 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086543 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLNA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086553 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLNA 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086585 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLNA 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086586 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLNA 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086635 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLNA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087301 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLRT1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087650 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLRT1 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088732 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLRT2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087388 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLRT3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 receptor-type tyrosine-protein kinase flt3 measurement http://www.ebi.ac.uk/efo/EFO_0020703 GCST90087389 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLRT3 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 receptor-type tyrosine-protein kinase flt3 measurement http://www.ebi.ac.uk/efo/EFO_0020703 GCST90090527 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLT1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090064 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLT3 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088385 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLT3LG 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087776 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLT3LG 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088209 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLT4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087934 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FLVCR1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090488 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDK1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088965 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDK2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087125 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PDLIM1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086738 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APP 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088243 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APPL1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087252 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein APRT 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086227 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AQP4 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086707 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARAF 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087085 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein AREG 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088156 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARF3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087082 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARF6 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086973 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARFGAP1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086794 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARFGAP2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086844 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARFIP1 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087474 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARFIP2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087111 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARG1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089227 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGAP1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086893 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGAP1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090836 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGAP25 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086690 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGAP30 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087240 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGAP36 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089340 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGAP45 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087517 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGAP5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087918 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGDIA 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089436 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGDIB 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090858 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGEF1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087692 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGEF10 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090481 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGEF2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087267 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGEF25 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087502 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARHGEF7 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087664 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARID1A 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090896 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARID3A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088561 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARL1 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086953 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARL11 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086980 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARL2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087087 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARL3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087075 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARL6IP5 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087488 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARL8B 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090230 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARMC10 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090512 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARMC5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090296 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARMC5 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090316 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARMC5 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090926 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARPC1B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087155 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARPC3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087535 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARPP19 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088829 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARPP21 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087275 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARRB1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087119 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARRDC3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086928 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARSA 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088442 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARSA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090299 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARSB 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088244 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ARSK 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090094 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ART3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086520 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS27A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088102 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS27A 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088705 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088881 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS3A 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089057 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS4X 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090805 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS6KA1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086915 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS6KA3 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088402 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS6KA5 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088554 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS6KA6 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087154 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS6KB1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086867 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS6KB1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090412 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPS7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088553 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RPSA 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088824 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RRAGC 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087061 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RRAS2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086933 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RRBP1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090717 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RRBP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090905 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RRM1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086705 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RRM2B 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090342 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RRM2B 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090386 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RS1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089462 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089316 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO1 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089317 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO2 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088746 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein RSPO2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090192 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL10 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 CXCL10 measurement http://www.ebi.ac.uk/efo/EFO_0010778 GCST90088599 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL11 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 CXCL11 measurement http://www.ebi.ac.uk/efo/EFO_0010779 GCST90088198 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL12 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CXCL12 measurement http://www.ebi.ac.uk/efo/EFO_0009420 GCST90087932 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL12 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CXCL12 measurement http://www.ebi.ac.uk/efo/EFO_0009420 GCST90088430 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL13 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 CXCL13 measurement http://www.ebi.ac.uk/efo/EFO_0009421 GCST90087621 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL13 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 CXCL13 measurement http://www.ebi.ac.uk/efo/EFO_0009421 GCST90088415 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL14 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089176 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL16 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087940 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL17 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090719 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL2;CXCL3 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088167 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL2;CXCL3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088236 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL5 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 CXCL5 measurement http://www.ebi.ac.uk/efo/EFO_0009422 GCST90088163 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL6 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 CXCL6 measurement http://www.ebi.ac.uk/efo/EFO_0009423 GCST90088419 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL8 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088392 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL9 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CXCL9 measurement http://www.ebi.ac.uk/efo/EFO_0010780 GCST90086814 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL9 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 CXCL9 measurement http://www.ebi.ac.uk/efo/EFO_0010780 GCST90090543 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYB561D1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087409 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYB5A 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086665 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYB5D2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086501 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYB5R3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089741 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYCS 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088138 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYGB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086789 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYP3A4 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088139 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CYP3A4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089896 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FTCD 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090556 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FTH1;FTL 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088192 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FTH1;FTL 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089242 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FTMT 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090013 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FURIN 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089333 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FUT10 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089701 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FUT2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090521 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FUT3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088733 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FUT5 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088734 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FUT8 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090074 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FUT9 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089606 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FXN 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086871 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FXR1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087360 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FXYD4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086302 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FXYD5 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086373 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FYN 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase FYN measurement http://www.ebi.ac.uk/efo/EFO_0020823 GCST90088525 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FYN 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 tyrosine-protein kinase FYN measurement http://www.ebi.ac.uk/efo/EFO_0020823 GCST90088735 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein FZD10 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086835 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein G0S2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090389 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein G3BP2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090844 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAA 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090674 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GABARAPL1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087133 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GABARAPL2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087024 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GABBR1 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086657 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GABBR2 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087677 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GABBR2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090916 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSE 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088449 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSF 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090179 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSF 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090555 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSG 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087939 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSH 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088501 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSH 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090207 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSH 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090246 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSH 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090247 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090692 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSL 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090599 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSO 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090593 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088251 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSV 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088344 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSZ 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088836 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTXN3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086287 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CUBN 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087300 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CUEDC2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089390 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CUL3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086203 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CUL4B 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087654 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CUL9 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087333 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CUZD1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089938 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CX3CL1 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 CX3CL1 measurement http://www.ebi.ac.uk/efo/EFO_0009419 GCST90088088 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXADR 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086608 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXADR 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090589 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CXCL1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 CXCL1 measurement http://www.ebi.ac.uk/efo/EFO_0010777 GCST90088166 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCK 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087322 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCKR 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088961 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCNT1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089623 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCNT2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089690 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCNT4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086470 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCNT4 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086475 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCSH 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086514 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087138 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF10 5,332 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089471 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF11 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90086913 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF11 5,333 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90087873 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF11 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90087874 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF11 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90087876 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF11 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 growth/differentiation factor 11 measurement http://www.ebi.ac.uk/efo/EFO_0020427 GCST90088059 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF15 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90088672 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF2 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 growth/differentiation factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020428 GCST90088792 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF5 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 growth/differentiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020429 GCST90088050 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDF9 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 growth/differentiation factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020430 GCST90088219 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDI2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088004 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GDNF 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089216 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GEM 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087247 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GFAP 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90088195 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GFRA1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088308 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GFRA2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087954 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GFRA3 5,325 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087952 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAD1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086658 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GADD45GIP1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090615 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAL 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087416 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAL3ST1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090264 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAL3ST2 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086427 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALE 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086756 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALK1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086751 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT1 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089654 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT10 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089613 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT11 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090267 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT13 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086496 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT16 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090384 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089206 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT3 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089517 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALNT7 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086485 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GALP 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090682 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAN 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086209 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAPDH 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 glyceraldehyde-3-phosphate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0020411 GCST90088545 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAPDHS 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089978 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GAS1 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089044 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GBP6 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089855 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GC 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089511 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087091 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCG 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088797 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GCH1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086595 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CSTL1 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089372 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CT55 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090658 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTAG1A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089576 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTBP1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086616 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTBS 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089286 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTCF 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087889 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTF1 5,329 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087645 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTF1 5,327 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088124 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTGF 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088160 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTHRC1 5,335 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089313 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTLA4 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088185 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTNNA2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090876 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTNNB1 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090193 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTNNB1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090194 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTNNB1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090854 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTRB1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089120 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTRB2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089138 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTRC 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089102 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTRL 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090567 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSA 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088250 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSB 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088216 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSB 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089981 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSC 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087643 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSC 5,330 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088249 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein CTSD 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089067 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GFRAL 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089569 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GGA1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087549 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GGA3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086855 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GGH 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090663 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GGT2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089353 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GH1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090204 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GH2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086525 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GHDC 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090787 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GHR 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088143 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GHRH 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090714 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GHRL 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089472 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GHRL 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090199 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GHRL 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090544 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein GIP 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089199 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLG 5,338 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088606 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLAU 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088614 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLAUR 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088006 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLBD1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089349 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLBD2 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089483 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLCB1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086701 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLCG1 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088744 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLCG2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086215 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLD3 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086510 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLD5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090038 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLEK 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089894 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLEKHA1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087001 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLEKHA4 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086506 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLEKHA7 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087191 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLG 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088493 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PLG 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088607 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRN1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086669 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRN1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086809 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRN3 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086289 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRTM1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088694 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRTM2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089558 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRTM3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088695 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRTM4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089504 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRRTM4 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090249 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRTM1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090661 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LRTM2 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090375 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LSAMP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088177 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LST1 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090739 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTA;LTB 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088425 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTA;LTB 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088426 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTA;LTB 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088758 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTA4H 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088268 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTB4R 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087466 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTBP4 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086634 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTBP4 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087397 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein LTBR 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087996 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG11 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089872 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089402 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089430 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG4 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089121 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090624 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG6 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089438 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG7 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089123 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG8 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089315 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSG9 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090637 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMA1 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088551 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMA1 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089897 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMA2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088650 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMA4 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087781 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMA6 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088552 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMA7 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087002 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMB1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087098 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMB5 5,344 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087083 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMB6 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086325 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSMD1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086428 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP7 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088072 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP7 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090213 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP8 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088148 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP8 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090532 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMP9 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087966 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMRN2 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086880 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRPF6 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090763 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRPS1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086719 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRPSAP1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090710 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRR16 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086372 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRR27 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090777 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRRG1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090117 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRRG1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090444 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRRG4 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090311 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRRG4 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090761 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088206 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088888 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS22 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088723 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS27 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088465 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS3 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088409 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS35 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090946 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS37 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089124 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS57 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090145 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRSS8 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089304 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRTN3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087634 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PRTN3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088429 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSAP 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089295 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSAPL1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090315 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSCA 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086358 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSD 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087352 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein PSD2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090520 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MMRN2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090785 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MNX1 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090758 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MOB1A 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086974 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MOCS3 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087842 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPDZ 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087732 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPG 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086984 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPL 5,326 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088406 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPO 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 myeloperoxidase (MPO)-DNA complex measurement http://www.ebi.ac.uk/efo/EFO_0011039 GCST90087967 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPP6 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087475 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPP7 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087192 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPST 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087152 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPZ 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086368 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MPZL2 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090664 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRAP 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089910 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRAP2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086486 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRC1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087997 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRC2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088200 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRE11A 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086683 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRM3 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090766 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL14 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089992 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL21 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090394 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL32 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089964 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL33 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087451 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL34 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089578 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL52 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089673 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL55 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086559 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRPL58 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089382 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRRF 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086929 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MRVI1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090082 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSH2 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090791 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSLN 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088571 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSLN 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088572 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSMB 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086371 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSMP 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090037 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSN 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088867 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSR1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086610 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSR1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086660 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSR1 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088487 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSRA 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089685 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSRB3 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089859 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MST1 5,368 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088680 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MST1R 5,341 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087999 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSTN 5,350 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086914 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MSTN 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087875 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MT1F 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086255 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTAP 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090904 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTCP1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087305 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTFR1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090505 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTHFD1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087079 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTHFS 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087789 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNB3 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90089830 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFS 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087076 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EGF 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006900 GCST90086891 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EGF 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006900 GCST90089068 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EGFLAM 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086919 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EGFR 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90088013 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EGFR 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90089002 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EGLN1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090899 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EHBP1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087244 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EHD4 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086734 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EHF 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087414 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EHMT2 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089220 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EID3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090036 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF1AD 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087518 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF1AX 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090862 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF1B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087167 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF2AK4 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087856 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF2B1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086221 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF3G 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086754 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF3J 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087482 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF4A3 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088857 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF4B 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087903 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF4E2 5,352 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090794 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF4EBP2 5,337 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088621 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF4G2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088632 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDDM3B 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089828 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDF1 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086967 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDIL3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090655 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDN1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089460 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDN2 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087078 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDN3 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089285 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EEA1 5,348 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087738 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EEF1B2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089230 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EEF2K 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086916 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFCAB14 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086465 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFCAB14 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090731 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFEMP1 5,346 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090216 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNA2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086453 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNA2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087802 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNA3 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087822 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNA3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089203 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNA4 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ephrin-A4 measurement http://www.ebi.ac.uk/efo/EFO_0020356 GCST90087743 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNA4 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ephrin-A4 measurement http://www.ebi.ac.uk/efo/EFO_0020356 GCST90087980 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNA5 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ephrin-A5 measurement http://www.ebi.ac.uk/efo/EFO_0020357 GCST90087981 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNB1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087376 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNB1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089191 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNB2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90087807 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNB2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90090281 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNB2 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90090287 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EFNB3 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90087953 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF4G3 5,342 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087703 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF4H 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089231 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF5 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087979 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF5A 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089232 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EIF5A2 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086702 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELANE 5,349 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087599 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELANE 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088998 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELAVL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086813 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELF5 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087453 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELK1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086178 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELK3 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089159 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELL 5,339 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086758 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELL2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086770 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ELMO1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087213 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EMC1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086898 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EMC4 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087499 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EMID1 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087338 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EMID1 5,356 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090748 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EMILIN3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090288 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EMILIN3 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090414 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EMILIN3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090951 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENAH 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090804 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENDOU 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089126 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ENG 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088804 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein S100A2 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086895 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYCT1 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087515 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYDGF 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090580 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYL6B 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087840 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYNN 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086997 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYO6 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090892 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYOM2 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087510 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYOM3 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087686 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYRF 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090336 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYSM1 5,345 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086780 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DYNLT3 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087279 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein DYRK3 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088671 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EBI3 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086473 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EBI3;IL27 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088090 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ECE1 5,355 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088457 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ECE1 5,347 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090283 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ECEL1 5,320 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089646 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ECH1 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087134 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ECI2 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087274 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein ECM1 5,334 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088346 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087722 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDA 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088087 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDA2R 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088230 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDAR 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90088162 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDC4 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087356 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein EDDM3A 5,340 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090742 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTIF3 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089877 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTMR1 5,364 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086583 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTMR6 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90087055 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTPAP 5,343 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090459 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTRF1L 5,362 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086558 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MTX2 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090332 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUC1 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086374 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUC1 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086523 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUC1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086650 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUC1 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090535 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUC15 5,359 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089414 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUC4 5,357 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086391 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUCL1 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086522 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUL1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086577 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUL1 5,367 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090625 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUSK 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086790 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MUTYH 5,365 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086192 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MVK 5,354 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086725 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MXI1 5,353 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90090462 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MXRA7 5,366 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089979 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MXRA8 5,361 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086320 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MXRA8 5,358 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089612 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYB 5,363 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086825 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYBPC1 5,360 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90089780 Genome-wide genotyping array 2022-02-15 35078996 Gudjonsson A 2022-01-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35078996 A genome-wide association study of serum proteins reveals shared loci with common diseases. Serum levels of protein MYC 5,351 Icelandic ancestry individuals NA Illumina [7506463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90086240 Genome-wide genotyping array 2021-07-01 33713608 Graff M 2021-03-05 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33713608 Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. Height 41,389 African ancestry individuals 11,364 African ancestry individuals, 253,288 European ancestry individuals Affymetrix, Illumina [17972582] (imputed) 74 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90013466 Genome-wide genotyping array 2021-07-01 33713608 Graff M 2021-03-05 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33713608 Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. Height 16,021 African ancestry men 2,915 African ancestry men, up to 253,288 European ancestry men Affymetrix, Illumina [16055004] (imputed) 18 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90013467 Genome-wide genotyping array 2021-07-01 33713608 Graff M 2021-03-05 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33713608 Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry. Height 25,369 African ancestry women 8,449 African ancestry women, up to 253,288 European ancestry women Affymetrix, Illumina [19885954] (imputed) 30 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90013468 Genome-wide genotyping array 2021-07-01 33201861 Lahm H 2020-11-17 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/33201861 Congenital heart disease risk loci identified by genome-wide association study in European patients. Congenital heart disease 4,034 European ancestry cases, 8,486 European ancestry controls NA Affymetrix, Illumina [9216527] (imputed) 1 congenital heart disease http://www.ebi.ac.uk/efo/EFO_0005207 GCST011989 Genome-wide genotyping array 2021-07-01 33201861 Lahm H 2020-11-17 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/33201861 Congenital heart disease risk loci identified by genome-wide association study in European patients. Congenital heart disease (transposition of the great arteries) 399 European ancestry cases, 8,486 European ancestry controls NA Affymetrix, Illumina [9216527] (imputed) 2 transposition of the great arteries http://purl.obolibrary.org/obo/MONDO_0000153 GCST011988 Genome-wide genotyping array 2021-07-01 33201861 Lahm H 2020-11-17 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/33201861 Congenital heart disease risk loci identified by genome-wide association study in European patients. Congenital right-sided heart lesions 1,296 European ancestry cases, 8,486 European ancestry controls NA Affymetrix, Illumina [9216527] (imputed) 1 congenital right-sided heart lesions http://www.ebi.ac.uk/efo/EFO_0600032 GCST011987 Genome-wide genotyping array 2021-07-01 33201861 Lahm H 2020-11-17 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/33201861 Congenital heart disease risk loci identified by genome-wide association study in European patients. Congenital left-sided heart lesions 326 European ancestry cases, 8,486 European ancestry controls NA Affymetrix, Illumina [9216527] (imputed) 3 congenital left-sided heart lesions http://www.ebi.ac.uk/efo/EFO_0005938 GCST011986 Genome-wide genotyping array 2021-07-01 33201861 Lahm H 2020-11-17 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/33201861 Congenital heart disease risk loci identified by genome-wide association study in European patients. Congenital heart disease (septal defects) 1,074 European ancestry cases, 8,486 European ancestry controls NA Affymetrix, Illumina [9216527] (imputed) 5 heart septal defect http://purl.obolibrary.org/obo/MONDO_0002078 GCST011985 Genome-wide genotyping array 2021-07-01 33201861 Lahm H 2020-11-17 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/33201861 Congenital heart disease risk loci identified by genome-wide association study in European patients. Congenital heart disease (anomalies of thoracic arteries and veins) 486 European ancestry cases, 8,486 European ancestry controls NA Affymetrix, Illumina [9216527] (imputed) 2 Abnormal cardiovascular system morphology http://purl.obolibrary.org/obo/HP_0030680 GCST011984 Genome-wide genotyping array 2021-08-27 33751636 Wei Y 2021-03-09 Biom J www.ncbi.nlm.nih.gov/pubmed/33751636 Confident identification of subgroups from SNP testing in RCTs with binary outcomes. Response to antioxidants and zinc in age-related macular degeneration (disease progression) 450 European ancestry AREDS formula treated cases, 677 European ancestry placebo treated cases NA Illumina [3895495] 2 disease progression measurement, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0008336, http://purl.obolibrary.org/obo/GO_0009410 GCST012255 Genome-wide genotyping array 2021-08-27 33757599 Ramanan VK 2021-03-23 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/33757599 Coping with brain amyloid: genetic heterogeneity and cognitive resilience to Alzheimer's pathophysiology. Cognitive resilience in amyloidosis 546 individuals 545 individuals Illumina [4456454] (imputed) 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST012254 Genome-wide genotyping array 2021-02-20 33589841 Chia R 2021-02-15 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33589841 Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture. Dementia with Lewy bodies 2,591 European ancestry cases, 4,027 European ancestry controls 970 European ancestry cases, 8,928 European ancestry controls NR [20137051] 5 Lewy body dementia http://www.ebi.ac.uk/efo/EFO_0006792 GCST90001390 Genome-wide sequencing 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(34:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060639 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(34:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 22 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060638 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(38:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060684 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(38:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060679 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(39:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060706 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(39:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 67 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060699 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(40:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060722 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(40:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060716 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(40:5)_[M+OAc]1-/Phosphatidylglycerol(39:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 32 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060824 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(41:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 50 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060745 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(41:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060737 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(42:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060775 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(42:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060769 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(42:3)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060763 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(43:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 63 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060793 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(43:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060788 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(43:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060781 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(43:6)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060895 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(44:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060826 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(44:5)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060820 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(44:6)_[M+OAc]1-/Phosphatidylglycerol(43:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 11 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060917 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(45:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060853 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(45:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060848 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(45:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 6 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060843 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(45:6)_[M+OAc]1-/Phosphatidylglycerol(44:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060938 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(20:3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 18 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060117 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(20:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 5 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060581 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(20:4)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 41 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060116 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(20:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 69 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060580 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(20:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060579 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(21:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060582 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:0)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060131 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060586 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060130 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:4)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060129 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 61 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060585 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:5)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060127 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 49 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060584 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:6)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 13 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060125 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(22:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060583 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(23:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060587 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(24:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060590 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(24:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060588 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Hydroxycholesterol_[M+H-2H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 sterol measurement http://www.ebi.ac.uk/efo/EFO_0010231 GCST90060132 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Hydroxycholesterol_[M+H-2H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sterol measurement http://www.ebi.ac.uk/efo/EFO_0010231 GCST90060589 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_15:0_[M+H]1+/Lysophosphatidylethanolamine_18:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060145 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_15:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060165 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_16:0_[M+H]1+/Lysophosphatidylethanolamine_19:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 7 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060150 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_16:1_[M+H]1+/Lysophosphatidylethanolamine_19:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060148 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_17:0_[M+H]1+/Lysophosphatidylethanolamine_20:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060157 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060774 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:3)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060768 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(37:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 65 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060674 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(37:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 136 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060700 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(37:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060817 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(38:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 27 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060728 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(38:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060849 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(38:1)_[M+CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 8 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060695 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(38:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 60 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060723 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(38:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060844 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(39:0)_[M+H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060753 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(39:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 64 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060717 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(39:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 113 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060752 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(39:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060863 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(39:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060860 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(39:6)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060731 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(39:7)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060726 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:0)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060754 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060783 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060891 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060746 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060776 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060887 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:2)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060742 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060770 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060884 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:3)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060764 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:3)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060881 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:6)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060873 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(40:7)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060758 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:0)_[M+H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060814 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060913 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060771 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 17 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060813 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060909 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:2)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060765 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:2)_[M+H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060803 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 31 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060808 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(41:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060904 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060935 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060809 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060840 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060933 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060835 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060928 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:3)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 71 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060830 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:3)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060924 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 59 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060827 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:8)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060812 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:8)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060908 Genome-wide genotyping array 2021-10-21 34404834 Sin S 2021-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34404834 A genome-wide association study of quantitative computed tomographic emphysema in Korean populations. Emphysema 514 Korean ancestry COPD individuals, 34 Korean ancestry non COPD individuals NA NR [599248] (imputed) 11 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90027902 Genome-wide genotyping array 2021-10-21 34404834 Sin S 2021-08-17 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34404834 A genome-wide association study of quantitative computed tomographic emphysema in Korean populations. Emphysema in chronic obstructive pulmonary disease 514 Korean ancestry individuals NA NR [599248] (imputed) 5 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90027903 Genome-wide genotyping array 2022-01-19 34737962 Lin X 2021-10-19 Front Oncol www.ncbi.nlm.nih.gov/pubmed/34737962 A Germline Variant at 8q24 Contributes to the Serum p2PSA Level in a Chinese Prostate Biopsy Cohort. Serum p2 prostate specific antigen levels 886 Chinese ancestry individuals 1,128 Chinese ancestry individuals Illumina [17098949] (imputed) 1 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST90091825 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_50:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060477 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_50:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060473 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_50:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060468 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_50:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060466 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_50:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060463 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_51:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060500 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_51:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060497 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_51:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060494 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_51:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060491 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_52:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060517 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_52:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060515 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_52:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060511 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_52:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 17 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060509 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_52:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060508 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_52:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060506 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_52:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060504 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_53:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060531 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_53:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 13 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060528 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_53:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060524 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_53:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060520 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_54:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060547 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_54:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060544 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_54:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060541 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_54:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060540 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_54:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060539 Genome-wide genotyping array 2021-06-01 33169155 Bigdeli TB 2020-11-10 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/33169155 Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans. Schizophrenia 44,794 European ancestry cases, 7,509 African American cases, 1,234 Latino cases, 112,777 European ancestry controls, 8,337 African American controls, 3,090 Latino controls NA Affymetrix [up to 49134253] (imputed) 24 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST011769 Genome-wide genotyping array 2021-06-01 33169155 Bigdeli TB 2020-11-10 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/33169155 Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans. Schizophrenia 37,759 European ancestry cases, 7,509 African American cases, 1,234 Latino cases, 22,778 East Asian ancestry cases, 91,590 European ancestry controls, 8,337 African American controls, 3,090 Latino controls, 35,362 East Asian ancestry controls NA Affymetrix [up to 49134253] (imputed) 20 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST011768 Genome-wide genotyping array 2021-06-01 33169155 Bigdeli TB 2020-11-10 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/33169155 Genome-Wide Association Studies of Schizophrenia and Bipolar Disorder in a Diverse Cohort of US Veterans. Bipolar disorder 24,267 European ancestry cases, 3,027 African American cases, 1,032 Latino cases, 79,492 European ancestry controls, 8,097 African American controls, 3,090 Latino controls NA Affymetrix [up to 49134253] (imputed) 10 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST011767 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Progesterone levels 4,097 individuals NA Affymetrix [10900000] (imputed) 6 progesterone measurement http://www.ebi.ac.uk/efo/EFO_0007004 GCST90094671 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Progesterone levels 2,220 men NA Affymetrix [10900000] (imputed) 1 progesterone measurement http://www.ebi.ac.uk/efo/EFO_0007004 GCST90094672 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Progesterone levels 1,877 women NA Affymetrix [10900000] (imputed) 5 progesterone measurement http://www.ebi.ac.uk/efo/EFO_0007004 GCST90094673 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. 17-hydroxyprogesterone (17-OHP) levels 3,549 individuals NA Affymetrix [10900000] (imputed) 3 17-hydroxyprogesterone measurement http://www.ebi.ac.uk/efo/EFO_0010220 GCST90094674 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. 17-hydroxyprogesterone (17-OHP) levels 2,220 men NA Affymetrix [10900000] (imputed) 4 17-hydroxyprogesterone measurement http://www.ebi.ac.uk/efo/EFO_0010220 GCST90094675 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. 17-hydroxyprogesterone (17-OHP) levels 1,329 women NA Affymetrix [10900000] (imputed) 2 17-hydroxyprogesterone measurement http://www.ebi.ac.uk/efo/EFO_0010220 GCST90094676 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Androstenedione levels 3,549 individuals NA Affymetrix [10900000] (imputed) 1 androstenedione measurement http://www.ebi.ac.uk/efo/EFO_0007972 GCST90094677 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Androstenedione levels 2,220 men NA Affymetrix [10900000] (imputed) 2 androstenedione measurement http://www.ebi.ac.uk/efo/EFO_0007972 GCST90094678 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Androstenedione levels 1,329 women NA Affymetrix [10900000] (imputed) 1 androstenedione measurement http://www.ebi.ac.uk/efo/EFO_0007972 GCST90094679 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Aldosterone levels 3,549 individuals NA Affymetrix [10900000] (imputed) 1 aldosterone measurement http://www.ebi.ac.uk/efo/EFO_0010219 GCST90094680 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Aldosterone levels 2,220 men NA Affymetrix [10900000] (imputed) 1 aldosterone measurement http://www.ebi.ac.uk/efo/EFO_0010219 GCST90094681 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Aldosterone levels 1,329 women NA Affymetrix [10900000] (imputed) 1 aldosterone measurement http://www.ebi.ac.uk/efo/EFO_0010219 GCST90094682 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Testosterone to estradiol ratio 5,696 individuals NA Affymetrix [10900000] (imputed) 2 estradiol measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004697, http://www.ebi.ac.uk/efo/EFO_0004908 GCST90094683 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Testosterone to estradiol ratio 3,413 men NA Affymetrix [10900000] (imputed) 1 estradiol measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004697, http://www.ebi.ac.uk/efo/EFO_0004908 GCST90094684 Genome-wide genotyping array 2022-02-18 34822396 Pott J 2021-10-28 Metabolites www.ncbi.nlm.nih.gov/pubmed/34822396 Sex-Specific Causal Relations between Steroid Hormones and Obesity-A Mendelian Randomization Study. Testosterone to estradiol ratio 2,283 women NA Affymetrix [10900000] (imputed) 0 estradiol measurement, testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004697, http://www.ebi.ac.uk/efo/EFO_0004908 GCST90094685 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation factor Xa measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019430 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Galectin-3-binding protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 galectin-3-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010241 GCST90019456 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-7 receptor subunit alpha measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 7 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008190 GCST90019457 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation factor IXab measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019458 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Prothrombin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019459 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement C2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019433 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. GDP-fucose protein O-fucosyltransferase 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019461 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement C1r subcomponent measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 complement C1r subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008090 GCST90019435 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation factor XIII B chain measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019463 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Angiostatin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 angiostatin measurement http://www.ebi.ac.uk/efo/EFO_0008024 GCST90019437 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Creatine kinase M-type:Creatine kinase B-type heterodimer measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019438 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement factor B measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 complement factor B measurement http://www.ebi.ac.uk/efo/EFO_0008096 GCST90019439 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Plasminogen measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 plasma plasminogen measurement http://www.ebi.ac.uk/efo/EFO_0006309 GCST90019440 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Thrombin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019441 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement factor H measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019442 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Serotransferrin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019443 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-1 receptor-like 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008168 GCST90019444 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. ERO1-like protein beta measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019471 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. C-reactive protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90019446 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement C1s subcomponent measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 complement C1s subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008091 GCST90019474 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Lactadherin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 lactadherin measurement http://www.ebi.ac.uk/efo/EFO_0008203 GCST90019448 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Monocyte differentiation antigen CD14 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019476 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Inter-alpha-trypsin inhibitor heavy chain H4 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019450 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Neuronal pentraxin-1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019478 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation Factor X measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019452 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Scavenger receptor class A member 5 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019380 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Heme oxygenase 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019406 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019382 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Catechol O-methyltransferase measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019408 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. SPARC-related modular calcium-binding protein 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019384 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Protein Z-dependent protease inhibitor measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019385 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation Factor VIII measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019386 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Ras-related protein Rab-1A measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019412 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation Factor XI measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019413 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Plakophilin-2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019389 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement component C8 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 complement component C8 measurement http://www.ebi.ac.uk/efo/EFO_0008094 GCST90019415 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-6 receptor subunit beta measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 6 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0008188 GCST90019416 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Vitamin K-dependent protein S measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019417 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. NADPH--cytochrome P450 reductase measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 NADPH--cytochrome P450 reductase measurement http://www.ebi.ac.uk/efo/EFO_0008242 GCST90019418 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Immunoglobulin G measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019419 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Alpha-galactosidase A measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019396 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Fibrinogen measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90019421 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-6 receptor subunit alpha measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90019398 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Gelsolin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019399 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Collagen alpha-1(VI) chain measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019400 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-1 receptor type 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019424 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-17 receptor A measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90019425 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation factor XIII measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019403 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. von Willebrand factor measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90019427 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Haptoglobin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90019428 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Lipopolysaccharide-binding protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019429 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Fibrinogen gamma chain measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90019455 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-2 receptor subunit alpha measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0010587 GCST90019431 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation factor VII measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019432 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-1 receptor antagonist protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90019460 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Insulin-degrading enzyme measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019434 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Procollagen galactosyltransferase 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019462 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Antithrombin-III measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019436 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. von Willebrand factor A domain-containing protein 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90019464 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Protein FAM162A measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019465 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019466 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. GrpE protein homolog 1, mitochondrial measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019467 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. von Willebrand factor A domain-containing protein 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90019468 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Inter-alpha-trypsin inhibitor heavy chain H3 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019469 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Haptoglobin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90019470 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. dCTP pyrophosphatase 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019445 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. KDEL motif-containing protein 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019472 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Sulfhydryl oxidase 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019473 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Growth/differentiation factor 15 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019447 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Endoplasmic reticulum lectin 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019475 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Gelsolin measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019449 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Palmitoyl-protein thioesterase 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019477 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation factor IX measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90019451 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Peptidyl-prolyl cis-trans isomerase FKBP7 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019479 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Coagulation Factor V measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST90019453 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. D-dimer measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019454 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. O-phosphoseryl-tRNA(Sec) selenium transferase measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019405 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Phospholipase D3 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019381 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Electron transfer flavoprotein subunit alpha, mitochondrial measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019407 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019383 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Amino-terminal enhancer of split measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019409 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Prostaglandin E synthase 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019410 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Serum amyloid A-2 protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019411 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. AP-2 complex subunit alpha-2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019387 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-1 Receptor accessory protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 1 Receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008167 GCST90019388 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Tissue-type plasminogen activator measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019414 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Rap1 GTPase-GDP dissociation stimulator 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019390 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-1 receptor type 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019391 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement component C8 gamma chain measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019392 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Stromal cell-derived factor 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019393 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Serum amyloid A-1 protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90019394 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Fibulin-5 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019395 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Apolipoprotein A-I measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019420 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Glutathione peroxidase 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019397 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Plasminogen activator inhibitor 1 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90019422 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Vitamin K-dependent protein C measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90019423 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Ras-related protein Rab-2A measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019401 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Monocyte differentiation antigen CD14, soluble measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019402 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-1 receptor-like 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 interleukin 1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0008169 GCST90019426 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Medium-chain specific acyl-CoA dehydrogenase, mitochondrial measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019404 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Interleukin-2 receptor subunit beta measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019480 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Complement C1r subcomponent-like protein measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019481 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Gamma-glutamyl hydrolase measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019482 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Vesicular integral-membrane protein VIP36 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019483 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. Eukaryotic translation initiation factor 4E type 2 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90019484 Genome-wide genotyping array 2021-06-25 33328453 Pietzner M 2020-12-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33328453 Genetic architecture of host proteins involved in SARS-CoV-2 infection. MAP/microtubule affinity-regulating kinase 3 measurement 10,708 European ancestry individuals NA Affymetrix, Illumina [17652797] (imputed) 0 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90019485 Genome-wide genotyping array 2021-10-04 34073884 Sasaki T 2021-05-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34073884 ALDH2 p.E504K Variation and Sex Are Major Factors Associated with Current and Quitting Alcohol Drinking in Japanese Oldest Old. Alcohol drinking status (current drinker vs non-current drinker) 408 Japanese ancestry current drinking cases, 607 Japanese ancestry non-current drinking controls NA Illumina [6380000] (imputed) 1 alcohol drinking http://www.ebi.ac.uk/efo/EFO_0004329 GCST012430 Genome-wide genotyping array 2021-06-23 34103634 Valette K 2021-06-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34103634 Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank. Asthma 56,167 White-British ancestry cases, 352,255 White-British ancestry controls NA Affymetrix [35186738] (imputed) 73 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90014325 Genome-wide genotyping array 2021-10-06 30255811 Restrepo NA 2018-09-14 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/30255811 Local genetic ancestry in CDKN2B-AS1 is associated with primary open-angle glaucoma in an African American cohort extracted from de-identified electronic health records. Glaucoma (primary open-angle) 138 African American cases, 1,376 African American controls NA Illumina [Metabochip] 0 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST012451 Targeted genotyping array [Metabochip] 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Cancer 56,634 White British ancestry cases, 218,196 White British ancestry controls NA NR [688737] 79 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90027051 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Breast cancer 10,682 White British ancestry cases, 138,504 White British ancestry controls NA NR [682398] 58 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90027052 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Chronic lymphocytic leukemia 764 White British ancestry cases, 272,079 White British ancestry controls NA NR [663083] 34 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90027053 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Colorectal cancer 3,351 White British ancestry cases, 271,479 White British ancestry controls NA NR [675173] 17 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90027054 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Epithelial ovarian cancer 1,112 White British ancestry cases, 147,944 White British ancestry controls NA NR [666300] 25 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90027055 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Lung cancer 2,479 White British ancestry cases, 272,351 White British ancestry controls NA NR [673172] 21 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90027056 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Melanoma 3,122 White British ancestry cases, 271,708 White British ancestry controls NA NR [674885] 56 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90027057 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Non-melanoma skin cancer 18,944 White British ancestry cases, 255,886 White British ancestry controls NA NR [685523] 157 non-melanoma skin carcinoma http://www.ebi.ac.uk/efo/EFO_0009260 GCST90027058 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Pancreatic cancer 768 White British ancestry cases, 264,559 White British ancestry controls NA NR [663102] 35 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90027059 Genome-wide genotyping array 2021-10-19 34290314 Brandes N 2021-07-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34290314 Genetic association studies of alterations in protein function expose recessive effects on cancer predisposition. Prostate cancer 7,438 White British ancestry cases, 118,206 White British ancestry controls NA NR [680312] 82 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90027060 Genome-wide genotyping array 2021-11-12 33713409 Chenoweth MJ 2021-03-13 Nicotine Tob Res www.ncbi.nlm.nih.gov/pubmed/33713409 A genome-wide association study of nausea incidence in varenicline-treated cigarette smokers. Nausea incidence in varenicline-treated smokers 57 European ancestry cases, 132 European ancestry controls NA Illumina [NR] (imputed) 11 response to varenicline, Nausea http://www.ebi.ac.uk/efo/EFO_0600052, http://purl.obolibrary.org/obo/HP_0002018 GCST90027236 Genome-wide genotyping array 2021-10-07 34117260 Chen G 2021-06-11 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/34117260 A UGT1A1 variant is associated with serum total bilirubin levels, which are causal for hypertension in African-ancestry individuals. Total bilirubin levels 1,127 West African individuals NA Affymetrix, Illumina [NR] (imputed) 2 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST012461 Genome-wide genotyping array 2021-06-01 33909500 Moll M 2021-04-28 Am J Physiol Lung Cell Mol Physiol www.ncbi.nlm.nih.gov/pubmed/33909500 A Systematic Analysis of Protein-altering Exonic Variants in Chronic Obstructive Pulmonary Disease. Chronic obstructive pulmonary disease up to 31,465 European ancestry cases, up to 203,688 European ancestry controls, up to 1,413 African ancestry cases, up to 6,080 African ancestry controls, up to 287 East Asian ancestry cases, up to 7,484 East Asian ancestry controls, up to 61 Hispanic cases, up to 613 Hispanic controls NA Illumina [at least 109036] 35 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST011766 Exome genotyping array [Exome array] 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Curly vs straight hair 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 1 hair shape measurement http://www.ebi.ac.uk/efo/EFO_0007824 GCST90026488 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Iris color 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 1 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST90026489 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Sunburn type 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 2 sunburn http://www.ebi.ac.uk/efo/EFO_0003958 GCST90026490 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Pigment spots (darkness) 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 1 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90026491 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Skin flushing frequency 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 3 Flushing http://purl.obolibrary.org/obo/HP_0031284 GCST90026492 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Rough skin frequency 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 1 skin roughness measurement http://www.ebi.ac.uk/efo/EFO_0600094 GCST90026493 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Response to cosmetics (uncomfortable frequency) 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 1 response to cosmetics http://www.ebi.ac.uk/efo/EFO_0600093 GCST90026494 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Pigment spots (number) 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 0 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90090981 Genome-wide genotyping array 2022-01-05 34265127 Inoue Y 2021-07-15 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/34265127 Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Pigment spots (size) 1,108 Japanese ancestry individuals NA Illumina [6258233] (imputed) 0 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90090982 Genome-wide genotyping array 2021-10-04 34022066 Kim KW 2021-05-22 Allergy www.ncbi.nlm.nih.gov/pubmed/34022066 Genome-wide association study identifies TNFSF15associated with childhood asthma. Asthma (childhood onset) 741 Korean ancestry cases, 1,140 Korean ancestry controls NA Affymetrix, Illumina [4559629] (imputed) 3 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST012429 Genome-wide genotyping array 2021-08-24 33542050 Namkoong H 2021-02-04 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33542050 Genome-wide association study in patients with pulmonary Mycobacterium avium complex disease. Pulmonary mycobacterium avium complex disease 475 Japanese ancestry cases, 417 Japanese ancestry controls 1,313 East Asian ancestry cases, 2,440 East Asian ancestry controls, 276 European ancestry cases, 206 European ancestry controls Affymetrix [5876247] (imputed) 1 Mycobacterium avium complex disease http://www.ebi.ac.uk/efo/EFO_0007386 GCST90026449 Genome-wide genotyping array 2021-10-01 34119372 Lord J 2021-05-04 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/34119372 A genome-wide association study of plasma phosphorylated tau181. Plasma p-tau181 levels 1,153 European ancestry individuals NA Illumina [5688385] (imputed) 2 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90027237 Genome-wide genotyping array 2022-03-09 35157032 Ramachandran D 2022-02-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35157032 Genome-wide association study and functional follow-up identifies 14q12 as a candidate risk locus for cervical cancer. Cervical cancer 363 German ancestry cases, 861 German ancestry controls NA Illumina [10000612] (imputed) 22 cervical cancer http://purl.obolibrary.org/obo/MONDO_0002974 GCST012776 Targeted genotyping array [Oncoarray] 2021-10-20 34112972 DeMichele-Sweet MAA 2021-06-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34112972 Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease. Psychosis in Alzheimer's disease 4,551 European ancestry cases, 5,796 European ancestry controls, 894 African American or unknown ancestry cases, 1,076 African American or unknown ancestry controls NA Illumina [7105229] (imputed) 31 psychotic symptoms http://www.ebi.ac.uk/efo/EFO_0005940 GCST90020050 Genome-wide genotyping array 2021-06-17 31784582 Chittoor G 2019-11-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31784582 Fine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study. Serum urate levels 2,000 American Indian individuals NA Illumina [162718] 2 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST011923 Targeted genotyping array [Metabochip] 2021-06-17 33955455 Beck JJ 2021-05-06 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33955455 Genetic Meta-Analysis of Twin Birth Weight Shows High Genetic Correlation with Singleton Birth Weight. Birth weight 42,212 European ancestry individuals NA Affymetrix, Illumina [7692335] (imputed) 2 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90000030 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (global efficiency) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026613 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (characteristic path length) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026614 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (louvain modularity) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026615 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (transitivity) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026616 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (local efficiency default) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026617 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (local efficiency dorsal attention) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026618 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (local efficiency frontoparietal) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026619 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (local efficiency limbic) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026620 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (local efficiency salience) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026621 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (local efficiency somatomotor) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026622 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (local effieiency visual) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026623 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (strength default) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026624 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (strength dorsal attention) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026625 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (strength frontoparietal) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026626 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (strength limbic) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026627 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (strength salience) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026628 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (strength somatomotor) 18,445 British ancestry individuals NA Affymetrix [9926107] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026629 Genome-wide genotyping array 2021-10-18 34272439 Foo H 2021-07-16 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34272439 Novel genetic variants associated with brain functional networks in 18,445 adults from the UK Biobank. Brain functional connectivity measurement (strength visual) 18,445 British ancestry individuals NA Affymetrix [9926108] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90026630 Genome-wide genotyping array 2021-07-27 34211149 Mills MC 2021-07-01 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34211149 Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Age at first sexual intercourse 214,547 European ancestry individuals NA NR [16567047] (imputed) 2 age at first sexual intercourse measurement http://www.ebi.ac.uk/efo/EFO_0009749 GCST90000045 Genome-wide genotyping array 2021-07-27 34211149 Mills MC 2021-07-01 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34211149 Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Age at first sexual intercourse 182,791 European ancestry individuals NA NR [16426330] (imputed) 8 age at first sexual intercourse measurement http://www.ebi.ac.uk/efo/EFO_0009749 GCST90000046 Genome-wide genotyping array 2021-07-27 34211149 Mills MC 2021-07-01 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34211149 Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Age at first sexual intercourse 397,338 European ancestry individuals NA NR [16516521] (imputed) 272 age at first sexual intercourse measurement http://www.ebi.ac.uk/efo/EFO_0009749 GCST90000047 Genome-wide genotyping array 2021-07-27 34211149 Mills MC 2021-07-01 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34211149 Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Age at first birth 418,758 European ancestry individuals NA NR [10813835] (imputed) 1 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST90000048 Genome-wide genotyping array 2021-07-27 34211149 Mills MC 2021-07-01 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34211149 Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Age at first birth 124,088 European ancestry individuals NA NR [9467402] (imputed) 1 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST90000049 Genome-wide genotyping array 2021-07-27 34211149 Mills MC 2021-07-01 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/34211149 Identification of 371 genetic variants for age at first sex and birth linked to externalising behaviour. Age at first birth 542,901 European ancestry individuals NA NR [9744772] (imputed) 88 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST90000050 Genome-wide genotyping array 2021-10-22 34216462 Pistoni L 2021-07-03 Carcinogenesis www.ncbi.nlm.nih.gov/pubmed/34216462 Associations between pancreatic expression quantitative traits and risk of pancreatic ductal adenocarcinoma. Pancreatic ductal adenocarcinoma 7,207 European ancestry cases, 7,062 European ancestry controls 2,039 Japanese ancestry cases, 32,592 Japanese ancestry controls, 4,467 cases, 4,130 controls Illumina [7509345] (imputed) 2 pancreatic ductal adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0002517 GCST90026648 Genome-wide genotyping array 2021-09-02 34018994 Xu JK 2021-03-22 Chin Med J (Engl) www.ncbi.nlm.nih.gov/pubmed/34018994 Genome-wide long non-coding RNA association study on Han Chinese women identifies lncHSAT164 as a novel susceptibility gene for breast cancer. Breast cancer 1,496 Han Chinese ancestry cases, 1,257 Han Chinese ancestry controls 4,138 Han Chinese ancestry cases, 5,051 Han Chinese ancestry controls Illumina [up to 800000] 4 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST012281 Targeted genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (2'-fucosyllactose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 2 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027203 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (3'-fucosyllactose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027219 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (3'-fucosyllactose) in secretors 305 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027222 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (3'-sialyllactose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027214 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (6'-sialyllactose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027215 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (difucosyllacto-N-hexaose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027221 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (difucosyllacto-N-hexaose) in non-secretors 90 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027227 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (difucosyllacto-N-tetrose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027205 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (difucosyllacto-N-tetrose) in secretors 305 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027223 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (difucosyllactose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027204 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (disialyllacto-N-hexaose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027216 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (disialyllacto-N-tetraose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027217 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (fucodisialyllacto-N-hexaose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027206 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (fucosyllacto-N-hexaose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 2 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027207 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-fucopentaose I) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027208 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-fucopentaose I) in secretors 305 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027224 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-fucopentaose II) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 2 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027209 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-fucopentaose II) in secretors 305 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027225 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-fucopentaose III) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 11 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027210 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-fucopentaose III) in non-secretors 90 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 44 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027228 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-fucopentaose III) in secretors 305 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 11 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027226 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-hexaose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 2 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027211 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-neotetraose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027218 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (lacto-N-tetrose) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027212 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (sialyl-lacto-N-tetraose b) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027213 Genome-wide genotyping array 2023-03-21 35535691 Narumi S 2022-05-10 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35535691 GWAS of thyroid dysgenesis identifies a risk locus at 2q33.3 linked to regulation of Wnt signaling. Thyroid dysgenesis 142 Japanese ancestry cases, 8,380 Japanese ancestry controls 80 German ancestry cases, 4,339 German ancestry controls NR [3445548] (imputed) 1 Congenital hypothyroidism due to developmental anomaly http://www.orpha.net/ORDO/Orphanet_95711 GCST90257013 Genome-wide genotyping array 2021-07-07 34035401 Dube MP 2021-05-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34035401 Genetics of symptom remission in outpatients with COVID-19. Symptoms in placebo-treated COVID-19 outpatients at risk of severe disease (time to remission) 851 European ancestry individuals NA Illumina [6392715] (imputed) 2 time to remission of COVID-19 symptoms, COVID-19, response to placebo http://www.ebi.ac.uk/efo/EFO_0600020, http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0008344 GCST012001 Genome-wide genotyping array 2021-07-07 34035401 Dube MP 2021-05-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34035401 Genetics of symptom remission in outpatients with COVID-19. COVID-19 (hospitalized vs not hospitalized) 58 European ancestry cases, 1,797 European ancestry controls NA Illumina [6393360] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST012000 Genome-wide genotyping array 2021-07-07 34035401 Dube MP 2021-05-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34035401 Genetics of symptom remission in outpatients with COVID-19. Symptoms in COVID-19 outpatients at risk of severe disease (time to remission) 1,723 European ancestry individuals NA Illumina [6392715] (imputed) 1 time to remission of COVID-19 symptoms, COVID-19 http://www.ebi.ac.uk/efo/EFO_0600020, http://purl.obolibrary.org/obo/MONDO_0100096 GCST012002 Genome-wide genotyping array 2021-09-20 34286861 Trendowski MR 2021-07-19 Cancer www.ncbi.nlm.nih.gov/pubmed/34286861 Clinical and genetic risk factors for radiation-associated ototoxicity: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort. Tinnitus in cranial radiation therapy-treated pediatric cancer survivors 146 European ancestry cases, 1,845 European ancestry controls 106 European ancestry cases, 846 European ancestry controls NR [9643440] (imputed) 0 Tinnitus, response to cranial radiation therapy http://purl.obolibrary.org/obo/HP_0000360, http://www.ebi.ac.uk/efo/EFO_0010950 GCST90027272 Genome-wide genotyping array 2021-09-20 34286861 Trendowski MR 2021-07-19 Cancer www.ncbi.nlm.nih.gov/pubmed/34286861 Clinical and genetic risk factors for radiation-associated ototoxicity: A report from the Childhood Cancer Survivor Study and the St. Jude Lifetime Cohort. Hearing loss in cranial radiation therapy-treated pediatric cancer survivors 270 European ancestry cases, 1,928 European ancestry controls 156 European ancestry cases, 175 European ancestry controls NR [9696169] (imputed) 0 hearing loss, response to cranial radiation therapy http://www.ebi.ac.uk/efo/EFO_0004238, http://www.ebi.ac.uk/efo/EFO_0010950 GCST90027273 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid vs negative) 9,913 European ancestry cases, 85,072 European ancestry controls, 2,553 Hispanic or Latin American cases, 13,086 Hispanic or Latin American controls, 506 Black or African American cases, 3,110 Black or African American controls NA Illumina [9939936] (imputed) 40 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027245 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (hospitalized covid vs population) 613 European ancestry cases, 680,416 European ancestry controls, 140 Hispanic or Latin American cases, 94,327 Hispanic or Latin American controls, 49 Black or African American cases, 22,410 Black or African American controls NA Illumina [9875426] (imputed) 98 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027246 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid pneumonia vs population) 1,004 European ancestry cases, 680,354 European ancestry controls, 218 Hispanic or Latin American cases, 94,318 Hispanic or Latin American controls, 64 Black or African American cases, 22,412 Black or African American controls NA Illumina [9901720] (imputed) 72 pneumonia, COVID-19 http://www.ebi.ac.uk/efo/EFO_0003106, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027247 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid respiratory support vs population) 495 European ancestry cases, 680,440 European ancestry controls, 102 Hispanic or Latin American cases, 94,330 Hispanic or Latin American controls, 39 Black or African American cases, 22,410 Black or African American controls NA Illumina [9842460] (imputed) 82 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027248 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (severe respiratory symptoms vs population) 1,128 European ancestry cases, 679,531 European ancestry controls, 245 Hispanic or Latin American cases, 94,237 Hispanic or Latin American controls, 74 Black or African American cases, 22,383 Black or African American controls NA Illumina [9906551] (imputed) 52 respiratory symptom measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0007939, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027249 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid vs negative) 9,913 European ancestry cases, 85,072 European ancestry controls NA Illumina [31704722] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027250 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (hospitalized covid vs population) 613 European ancestry cases, 680,416 European ancestry controls NA Illumina [21433846] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027251 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid pneumonia vs population) 1,004 European ancestry cases, 680,354 European ancestry controls NA Illumina [23640711] (imputed) 1 pneumonia, COVID-19 http://www.ebi.ac.uk/efo/EFO_0003106, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027252 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid respiratory support vs population) 495 European ancestry cases, 680,440 European ancestry controls NA Illumina [20506675] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027253 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (severe respiratory symptoms vs population) 1,128 European ancestry cases, 679,531 European ancestry controls NA Illumina [2412076] (imputed) 1 respiratory symptom measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0007939, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027254 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid vs negative) 2,553 Hispanic or Latin American cases, 13,086 Hispanic or Latin American controls NA Illumina [35218582] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027255 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (hospitalized covid vs population) 140 Hispanic or Latin American cases, 94,327 Hispanic or Latin American controls NA Illumina [20840951] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027256 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid pneumonia vs population) 218 Hispanic or Latin American cases, 94,318 Hispanic or Latin American controls NA Illumina [23268376] (imputed) 0 pneumonia, COVID-19 http://www.ebi.ac.uk/efo/EFO_0003106, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027257 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid respiratory support vs population) 102 Hispanic or Latin American cases, 94,330 Hispanic or Latin American controls NA Illumina [19031602] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027258 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (severe respiratory symptoms vs population) 245 Hispanic or Latin American cases, 94,237 Hispanic or Latin American controls NA Illumina [2397628] (imputed) 0 respiratory symptom measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0007939, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027259 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid vs negative) 506 Black or African American cases, 3,110 Black or African American controls NA Illumina [31623562] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027260 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (hospitalized covid vs population) 49 Black or African American cases, 22,410 Black or African American controls NA Illumina [21980587] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027261 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid pneumonia vs population) 64 Black or African American cases, 22,412 Black or African American controls NA Illumina [23342614] (imputed) 0 pneumonia, COVID-19 http://www.ebi.ac.uk/efo/EFO_0003106, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027262 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (covid respiratory support vs population) 39 Black or African American cases, 22,410 Black or African American controls NA Illumina [20847880] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027263 Genome-wide genotyping array 2021-09-09 33888907 Shelton JF 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888907 Trans-ancestry analysis reveals genetic and nongenetic associations with COVID-19 susceptibility and severity. COVID-19 (severe respiratory symptoms vs population) 74 Black or African American cases, 22,383 Black or African American controls NA Illumina [24042173] (imputed) 0 respiratory symptom measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0007939, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90027264 Genome-wide genotyping array 2021-10-04 34047840 Vicuna L 2021-05-28 Hum Genet www.ncbi.nlm.nih.gov/pubmed/34047840 Novel loci and mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys. Age at peak height velocity 440 Chilean boys, 464 Chilean girls NA Illumina [774433] (imputed) 1 growth rate measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0010572, http://www.ebi.ac.uk/efo/EFO_0008007 GCST012433 Genome-wide genotyping array 2021-10-04 34047840 Vicuna L 2021-05-28 Hum Genet www.ncbi.nlm.nih.gov/pubmed/34047840 Novel loci and mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys. Height at time of age with peak height velocity 440 Chilean boys, 464 Chilean girls NA Illumina [774433] (imputed) 0 growth rate measurement, age at assessment, body height http://www.ebi.ac.uk/efo/EFO_0010572, http://www.ebi.ac.uk/efo/EFO_0008007, http://www.ebi.ac.uk/efo/EFO_0004339 GCST012432 Genome-wide genotyping array 2021-10-04 34047840 Vicuna L 2021-05-28 Hum Genet www.ncbi.nlm.nih.gov/pubmed/34047840 Novel loci and mapuche genetic ancestry are associated with pubertal growth traits in Chilean boys. Peak height velocity 440 Chilean boys, 464 Chilean girls NA Illumina [774433] (imputed) 7 growth rate measurement http://www.ebi.ac.uk/efo/EFO_0010572 GCST012434 Genome-wide genotyping array 2022-08-15 34382107 Wei J 2021-08-11 Hernia www.ncbi.nlm.nih.gov/pubmed/34382107 Identification of fifty-seven novel loci for abdominal wall hernia development and their biological and clinical implications: results from the UK Biobank. Inguinal hernia 13,047 European ancestry cases, 262,499 European ancestry controls 4,450 European ancestry cases, 87,398 European ancestry controls Affymetrix [8568156] (imputed) 2113 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90027168 Genome-wide genotyping array 2022-08-15 34382107 Wei J 2021-08-11 Hernia www.ncbi.nlm.nih.gov/pubmed/34382107 Identification of fifty-seven novel loci for abdominal wall hernia development and their biological and clinical implications: results from the UK Biobank. Femoral hernia 590 European ancestry cases, 274,956 European ancestry controls 218 European ancestry cases, 91,630 European ancestry controls Affymetrix [8568156] (imputed) 23 femoral hernia http://www.ebi.ac.uk/efo/EFO_1001791 GCST90027169 Genome-wide genotyping array 2022-08-15 34382107 Wei J 2021-08-11 Hernia www.ncbi.nlm.nih.gov/pubmed/34382107 Identification of fifty-seven novel loci for abdominal wall hernia development and their biological and clinical implications: results from the UK Biobank. Umbilical hernia 3,211 European ancestry cases, 272,335 European ancestry controls 1,078 European ancestry cases, 90,770 European ancestry controls Affymetrix [8568156] (imputed) 311 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90027170 Genome-wide genotyping array 2022-08-15 34382107 Wei J 2021-08-11 Hernia www.ncbi.nlm.nih.gov/pubmed/34382107 Identification of fifty-seven novel loci for abdominal wall hernia development and their biological and clinical implications: results from the UK Biobank. Ventral hernia 2,704 European ancestry cases, 272,842 European ancestry controls 955 European ancestry cases, 90,893 European ancestry controls Affymetrix [8568156] (imputed) 36 ventral hernia http://www.ebi.ac.uk/efo/EFO_1001866 GCST90027171 Genome-wide genotyping array 2021-10-21 34159505 Wang H 2021-06-16 Sci China Life Sci www.ncbi.nlm.nih.gov/pubmed/34159505 Novel loci and potential mechanisms of major depressive disorder, bipolar disorder, and schizophrenia. Major depressive disorder (MTAG) 119,754 European ancestry individuals NA NR [2625067] 11 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90020093 Genome-wide genotyping array 2021-10-21 34159505 Wang H 2021-06-16 Sci China Life Sci www.ncbi.nlm.nih.gov/pubmed/34159505 Novel loci and potential mechanisms of major depressive disorder, bipolar disorder, and schizophrenia. Bipolar disorder (MTAG) 1,450,972 European ancestry individuals NA NR [2625067] 49 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90020094 Genome-wide genotyping array 2021-10-21 34159505 Wang H 2021-06-16 Sci China Life Sci www.ncbi.nlm.nih.gov/pubmed/34159505 Novel loci and potential mechanisms of major depressive disorder, bipolar disorder, and schizophrenia. Schizophrenia (MTAG) 940,613 European ancestry individuals NA NR [2625067] 90 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90020095 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombin generation parameter (lagtime) 327 European ancestry individuals NA Illumina [7000000] (imputed) 1 thrombin generation potential measurement http://www.ebi.ac.uk/efo/EFO_0005538 GCST90052889 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombomodulin modified thrombin generation parameter (lagtime) 327 European ancestry individuals NA Illumina [7000000] (imputed) 1 thrombin generation potential measurement, thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0005538, http://www.ebi.ac.uk/efo/EFO_0007774 GCST90052890 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombin generation parameter (time to peak thrombin generation) 327 European ancestry individuals NA Illumina [7000000] (imputed) 1 thrombin generation potential measurement http://www.ebi.ac.uk/efo/EFO_0005538 GCST90052891 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombomodulin modified thrombin generation parameter (time to peak thrombin generation) 327 European ancestry individuals NA Illumina [7000000] (imputed) 0 thrombin generation potential measurement, thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0005538, http://www.ebi.ac.uk/efo/EFO_0007774 GCST90052892 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombin generation parameter (peak thrombin generation) 327 European ancestry individuals NA Illumina [7000000] (imputed) 1 thrombin generation potential measurement http://www.ebi.ac.uk/efo/EFO_0005538 GCST90052893 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombomodulin modified thrombin generation parameter (peak thrombin generation) 327 European ancestry individuals NA Illumina [7000000] (imputed) 0 thrombin generation potential measurement, thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0005538, http://www.ebi.ac.uk/efo/EFO_0007774 GCST90052894 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombin generation parameter (endogenous thrombin potential) 327 European ancestry individuals NA Illumina [7000000] (imputed) 2 thrombin generation potential measurement http://www.ebi.ac.uk/efo/EFO_0005538 GCST90052895 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombomodulin modified thrombin generation parameter (endogenous thrombin potential) 327 European ancestry individuals NA Illumina [7000000] (imputed) 2 thrombin generation potential measurement, thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0005538, http://www.ebi.ac.uk/efo/EFO_0007774 GCST90052896 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombomodulin sensitivity ratio (normalized endogenous thrombin potential to thrombomodulin) 327 European ancestry individuals NA Illumina [7000000] (imputed) 2 thrombin generation potential measurement, thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0005538, http://www.ebi.ac.uk/efo/EFO_0007774 GCST90052897 Genome-wide genotyping array 2021-11-03 34532976 Wan J 2021-09-17 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/34532976 Kallikrein augments the anticoagulant function of the protein C system in thrombin generation. Thrombomodulin sensitivity ratio (normalized peak thrombin generation to thrombomodulin) 327 European ancestry individuals NA Illumina [7000000] (imputed) 1 thrombin generation potential measurement, thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0005538, http://www.ebi.ac.uk/efo/EFO_0007774 GCST90052898 Genome-wide genotyping array 2021-12-03 34274964 Duijvenboden S 2021-07-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34274964 Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders. QT interval 52,107 European ancestry individuals 48,997 individuals Affymetrix [9800000] 11 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90026650 Genome-wide genotyping array 2021-12-03 34274964 Duijvenboden S 2021-07-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34274964 Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders. QT interval 24,495 European ancestry men NA Affymetrix [NR] 29 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90026651 Genome-wide genotyping array 2021-12-03 34274964 Duijvenboden S 2021-07-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34274964 Genomic and pleiotropic analyses of resting QT interval identifies novel loci and overlap with atrial electrical disorders. QT interval 27,612 European ancestry women NA Affymetrix [NR] 28 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90026652 Genome-wide genotyping array 2021-06-21 34011352 Schwarm C 2021-05-19 Orphanet J Rare Dis www.ncbi.nlm.nih.gov/pubmed/34011352 Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in Germans. Bullous pemphigoid 438 German cases, 417 German controls NA Affymetrix [up to 386296] (imputed) 13 bullous pemphigoid http://www.ebi.ac.uk/efo/EFO_0007187 GCST011940 Genome-wide genotyping array 2021-07-29 34247186 Wendel B 2021-07-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34247186 A genome-wide association study of the longitudinal course of executive functions. Executive function (trail making test B) x time interaction 1,272 European ancestry individuals NA Illumina [8241560] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90020165 Genome-wide genotyping array 2021-07-29 34247186 Wendel B 2021-07-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34247186 A genome-wide association study of the longitudinal course of executive functions. Executive function (trail making test B) 1,272 European ancestry individuals NA Illumina [8235300] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90020166 Genome-wide genotyping array 2021-07-29 34247186 Wendel B 2021-07-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34247186 A genome-wide association study of the longitudinal course of executive functions. Executive function (verbal digit span backwards test) x time interaction 1,297 European ancestry individuals NA Illumina [8241300] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90020167 Genome-wide genotyping array 2021-07-29 34247186 Wendel B 2021-07-10 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34247186 A genome-wide association study of the longitudinal course of executive functions. Executive function (verbal digit span backwards test) 1,297 European ancestry individuals NA Illumina [8241300] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90020168 Genome-wide genotyping array 2021-10-15 34343768 Chu X 2021-07-01 Sleep Med www.ncbi.nlm.nih.gov/pubmed/34343768 Insomnia affects the levels of plasma bilirubin and protein metabolism: an observational study and GWGEIS in UK Biobank cohort. Direct bilirubin levels x insomnia interaction 85,121 cases with insomnia, 74,733 controls without insomnia NA Affymetrix [NR] (imputed) 82 insomnia, bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004698, http://www.ebi.ac.uk/efo/EFO_0004570 GCST90026656 Genome-wide genotyping array 2021-10-15 34343768 Chu X 2021-07-01 Sleep Med www.ncbi.nlm.nih.gov/pubmed/34343768 Insomnia affects the levels of plasma bilirubin and protein metabolism: an observational study and GWGEIS in UK Biobank cohort. Total bilirubin levels x insomnia interaction 101,922 cases with insomnia, 84,871 controls with insomnia NA Affymetrix [NR] (imputed) 85 insomnia, bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004698, http://www.ebi.ac.uk/efo/EFO_0004570 GCST90026657 Genome-wide genotyping array 2021-10-15 34343768 Chu X 2021-07-01 Sleep Med www.ncbi.nlm.nih.gov/pubmed/34343768 Insomnia affects the levels of plasma bilirubin and protein metabolism: an observational study and GWGEIS in UK Biobank cohort. Total protein levels x insomnia interaction 93,452 cases with insomnia, 78,122 controls without insomnia NA Affymetrix [NR] (imputed) 266 insomnia, total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004698, http://www.ebi.ac.uk/efo/EFO_0004536 GCST90026658 Genome-wide genotyping array 2021-12-14 34260948 Cipriani V 2021-07-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260948 Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations. Complement factor H measurement 252 European ancestry individuals NA Illumina [NR] (imputed) 21 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90026527 Genome-wide genotyping array 2021-12-14 34260948 Cipriani V 2021-07-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260948 Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations. Complement factor H-like 1 protein levels 252 European ancestry individuals NA Illumina [NR] (imputed) 15 complement factor H-like 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0600092 GCST90026528 Genome-wide genotyping array 2021-12-14 34260948 Cipriani V 2021-07-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260948 Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations. Complement factor H-related protein 1 levels 252 European ancestry individuals NA Illumina [NR] (imputed) 36 complement factor H-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600054 GCST90026529 Genome-wide genotyping array 2021-12-14 34260948 Cipriani V 2021-07-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260948 Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations. Complement factor H-related protein 2 levels 252 European ancestry individuals NA Illumina [NR] (imputed) 23 complement factor H-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0600055 GCST90026530 Genome-wide genotyping array 2021-12-14 34260948 Cipriani V 2021-07-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260948 Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations. Complement factor H-related protein 3 levels 252 European ancestry individuals NA Illumina [NR] (imputed) 125 complement factor H-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0600056 GCST90026531 Genome-wide genotyping array 2021-12-14 34260948 Cipriani V 2021-07-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260948 Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations. Complement factor H-related protein 4 levels 252 European ancestry individuals NA Illumina [NR] (imputed) 31 complement factor H-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0600091 GCST90026532 Genome-wide genotyping array 2021-12-14 34260948 Cipriani V 2021-07-12 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34260948 Beyond factor H: The impact of genetic-risk variants for age-related macular degeneration on circulating factor-H-like 1 and factor-H-related protein concentrations. Complement factor H-related protein 5 levels 252 European ancestry individuals NA Illumina [NR] (imputed) 27 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90026533 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(15:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060570 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(16:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060572 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(16:0)-OH_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060106 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(16:1)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060102 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(16:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060571 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(16:1)-OH_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060104 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(16:2)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060101 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(16:3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060100 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(17:0)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060105 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(17:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060574 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(17:1)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060103 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(17:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060573 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060578 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:0)-OH_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060115 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:1)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060108 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060577 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:1)-OH_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060113 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060576 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:2)-OH_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060111 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060575 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(18:4)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060107 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(19:0)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060114 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(19:1)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060112 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(20:1)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060120 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(20:2)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060118 Genome-wide genotyping array 2021-10-27 34417961 Guo D 2021-08-21 Biol Trace Elem Res www.ncbi.nlm.nih.gov/pubmed/34417961 Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population. Copper levels 587 Han Chinese ancestry individuals NA Affymetrix [6423076] (imputed) 6 serum copper measurement http://www.ebi.ac.uk/efo/EFO_0005267 GCST90032165 Genome-wide genotyping array 2021-10-27 34417961 Guo D 2021-08-21 Biol Trace Elem Res www.ncbi.nlm.nih.gov/pubmed/34417961 Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population. Zinc levels 587 Han Chinese ancestry individuals NA Affymetrix [6423076] (imputed) 1 serum zinc measurement http://www.ebi.ac.uk/efo/EFO_0005268 GCST90032166 Genome-wide genotyping array 2021-10-27 34417961 Guo D 2021-08-21 Biol Trace Elem Res www.ncbi.nlm.nih.gov/pubmed/34417961 Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population. Calcium levels 587 Han Chinese ancestry individuals NA Affymetrix [6423076] (imputed) 4 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90032167 Genome-wide genotyping array 2021-10-27 34417961 Guo D 2021-08-21 Biol Trace Elem Res www.ncbi.nlm.nih.gov/pubmed/34417961 Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population. Serum magnesium levels 587 Han Chinese ancestry individuals NA Affymetrix [6423076] (imputed) 3 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST90032168 Genome-wide genotyping array 2021-10-27 34417961 Guo D 2021-08-21 Biol Trace Elem Res www.ncbi.nlm.nih.gov/pubmed/34417961 Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population. Iron levels 587 Han Chinese ancestry individuals NA Affymetrix [6423076] (imputed) 3 serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006332 GCST90032169 Genome-wide genotyping array 2021-10-27 34417961 Guo D 2021-08-21 Biol Trace Elem Res www.ncbi.nlm.nih.gov/pubmed/34417961 Preliminary study of genome-wide association identifies novel susceptibility genes for serum mineral elements in the Chinese Han population. Lead levels 587 Han Chinese ancestry individuals NA Affymetrix [6423076] (imputed) 2 blood lead measurement http://www.ebi.ac.uk/efo/EFO_0007040 GCST90032170 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(42:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060993 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(42:5)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 43 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060989 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(42:7)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 49 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060985 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(42:8)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060905 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(42:8)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060984 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(44:6)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 67 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90061008 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(44:9)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060944 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_32:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 41 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060225 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_32:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060268 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_32:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060224 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_33:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060229 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_33:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060286 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_34:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 37 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060241 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_34:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 33 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060239 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_34:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060309 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_34:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 33 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060235 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_34:2_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060305 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_35:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060252 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_35:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060335 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_36:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 29 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060269 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_36:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 35 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060266 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_36:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060363 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_36:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 37 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060263 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_36:2_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060357 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_36:3_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060351 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_37:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 14 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060281 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_38:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 64 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060306 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_38:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060413 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_38:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060302 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_38:2_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060409 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_39:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 35 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060328 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_39:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060441 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_39:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060323 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_40:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060364 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_40:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060358 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_40:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060467 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_40:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 19 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060352 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_40:2_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060464 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_40:3_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060348 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_40:3_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060460 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_41:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060386 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_41:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060383 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_41:2_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060489 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_42:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060410 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_42:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 10 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060403 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_42:2_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060507 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_42:3_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060399 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_42:3_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060505 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_43_2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 7 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060435 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin_43_2_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060522 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(35:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 19 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060890 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(36:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060920 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(36:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 44 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060992 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(36:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060916 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(36:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 68 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060988 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(36:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 369 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060912 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(36:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 10 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060907 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(36:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 50 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060903 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060958 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90061009 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060956 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060949 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:3)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90061007 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 104 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060946 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060943 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(38:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 7 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060942 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(40:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 19 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060979 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(40:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 67 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060976 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(40:7)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90061012 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(42:8)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90061002 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine_27:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060219 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine_36:1_[M+H]1+/Phosphatidylglycerol_36:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060366 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine_38:3_[M+H]1+/Phosphatidylglycerol_38:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060405 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine_40:3_[M+H]1+/Phosphatidylglycerol_40:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 17 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060461 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine_40:5_[M+H]1+/Phosphatidylglycerol_40:7_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060455 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:2_[M+H]1+/Phosphatidylethanolamine_38:2_[M+H]1+/Phosphatidate_40:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 28 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060325 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:2_[M+OAc]1-/Phosphatidylserine_39:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060439 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:3_[M+H]1+/Phosphatidylethanolamine_38:3_[M+H]1+/Phosphatidate_40:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 42 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060319 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:3_[M+OAc]1-/Phosphatidylserine_39:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060436 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:4_[M+H]1+/Phosphatidylethanolamine_38:4_[M+H]1+/Phosphatidate_40:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 54 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060316 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:4_[M+OAc]1-/Phosphatidylserine_39:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060432 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:5_[M+OAc]1-/Phosphatidylserine_39:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060427 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:6_[M+H]1+/Phosphatidylethanolamine_38:6_[M+H]1+/Phosphatidate_40:7_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 27 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060312 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:6_[M+OAc]1-/Phosphatidylserine_39:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060422 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:0_[M+H]1+/Phosphatidylethanolamine_39:0_[M+H]1+/Phosphatidate_41:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060368 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_36:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060472 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O_33:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060397 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O_33:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060394 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O_34:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060431 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O_34:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060426 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O_35:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060454 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O_36:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 22 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060480 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O_36:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060479 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O(33:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 39 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060825 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol-O(36:0)_[M-H]1-/Phosphatidylglycerol(37:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 63 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060898 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(32:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 7 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060819 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(33:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060857 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(34:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 12 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060877 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(34:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 19 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060872 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol(34:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 91 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060867 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine_44:7_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060529 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-O_36:2_[M+H]1+/Phosphatidylglycerol-O_36:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060330 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-O_38:2_[M+H]1+/Phosphatidylglycerol-O_38:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060388 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-O_38:4_[M+H]1+/Phosphatidylglycerol-O_38:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060381 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-O_38:5_[M+H]1+/Phosphatidylglycerol-P_38:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060377 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-O_40:4_[M+H]1+/Phosphatidylglycerol-O_40:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060433 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-O_40:5_[M+H]1+/Phosphatidylglycerol-P_40:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060428 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-O_42:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060475 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-P_42:1_[M+H]1+/Phosphatidylglycerol-P_42:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060482 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine-P_42:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060471 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(33:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060821 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(35:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 44 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060864 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(36:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060892 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(38:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060936 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(38:3)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060930 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(38:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060925 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(39:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060945 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(40:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060971 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(40:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060969 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(40:3)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060966 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(40:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060964 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(40:5)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060961 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(41:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060980 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(41:5)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060978 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylserine(42:3)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90060995 Genome-wide genotyping array 2021-11-10 29483669 Appel EVR 2018-02-26 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/29483669 Genetic determinants of glycated hemoglobin levels in the Greenlandic Inuit population. Glycated hemoglobin levels 4,049 individuals 6,006 European ancestry individuals Illumina [112277] 3 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST012499 Targeted genotyping array [Cardio-MetaboChip] 2021-09-14 34465887 Wu P 2021-08-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34465887 Trans-ethnic genome-wide association study of severe COVID-19. Severe COVID-19 infection 65 Chinese ancestry cases, 138 Chinese ancestry controls NA NR [5056041] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90014052 Genome-wide sequencing 2021-09-14 34465887 Wu P 2021-08-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34465887 Trans-ethnic genome-wide association study of severe COVID-19. Asymptomatic COVID-19 infection 63 Chinese ancestry cases, 140 Chinese ancestry controls NA NR [5056041] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90014053 Genome-wide sequencing 2022-10-06 34461747 Yu M 2021-08-31 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34461747 Genome-Wide Association Meta-Analysis Supports Genes Involved in Valve and Cardiac Development to Associate With Mitral Valve Prolapse. Mitral valve prolapse 1,920 European ancestry cases, 6,858 European ancestry controls NA Affymetrix, Illumina [8021974] (imputed) 10 Mitral valve prolapse http://purl.obolibrary.org/obo/HP_0001634 GCST90038453 Genome-wide genotyping array 2021-06-02 33937362 Moller PL 2021-04-16 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/33937362 Sortilin as a Biomarker for Cardiovascular Disease Revisited. Sortilin levels (ELISA) 1,173 European ancestry individuals NA Illumina [4658994] (imputed) 1 sortilin measurement http://www.ebi.ac.uk/efo/EFO_0600000 GCST90019034 Genome-wide genotyping array 2021-06-02 33937362 Moller PL 2021-04-16 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/33937362 Sortilin as a Biomarker for Cardiovascular Disease Revisited. Sortilin levels (OLINK) 1,173 European ancestry individuals NA Illumina [4658994] (imputed) 1 sortilin measurement http://www.ebi.ac.uk/efo/EFO_0600000 GCST90019035 Genome-wide genotyping array 2021-06-02 33937362 Moller PL 2021-04-16 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/33937362 Sortilin as a Biomarker for Cardiovascular Disease Revisited. Sortilin levels (ELISA) 1,173 European ancestry individuals NA Illumina [44377997] 0 sortilin measurement http://www.ebi.ac.uk/efo/EFO_0600000 GCST90019036 Genome-wide sequencing 2021-06-02 33937362 Moller PL 2021-04-16 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/33937362 Sortilin as a Biomarker for Cardiovascular Disease Revisited. Sortilin levels (OLINK) 1,173 European ancestry individuals NA Illumina [44377997] 0 sortilin measurement http://www.ebi.ac.uk/efo/EFO_0600000 GCST90019037 Genome-wide sequencing 2021-12-15 34861974 Mullins N 2021-09-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34861974 Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Suicide attempt 26,590 European ancestry cases, 492,022 European ancestry controls, 1,298 African American cases, 7,375 African American controls, 1,894 Asian American ancestry cases, 20,564 Asian American ancestry controls 14,089 European, Asian American, African American or Hispanic/Latino cases, 395,359 European, Asian American, African American or Hispanic/Latino controls Affymetrix, Illumina [7700000] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90091212 Genome-wide genotyping array, Genome-wide sequencing 2021-12-15 34861974 Mullins N 2021-09-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34861974 Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors. Suicide attempt 26,590 European ancestry cases, 492,022 European ancestry controls NA Affymetrix, Illumina [7700000] (imputed) 2 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90091213 Genome-wide genotyping array 2021-08-16 32675224 Thorball CW 2020-07-16 Haematologica www.ncbi.nlm.nih.gov/pubmed/32675224 Genetic variation near CXCL12 is associated with susceptibility to HIV-related non-Hodgkin lymphoma. Non-hodgkin's lymphoma in HIV infection 278 European ancestry cases, 1,924 European ancestry controls NA Illumina [6200000] (imputed) 1 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90025870 Genome-wide genotyping array 2021-06-17 34016946 Wu LS 2021-05-20 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34016946 Genome-wide association study of early-onset bipolar I disorder in the Han Taiwanese population. Bipolar disorder (early vs late onset) 516 Han Taiwanese ancestry cases, 790 Han Taiwanese ancestry controls 153 Han Taiwanese ancestry cases, 320 Han Taiwanese ancestry controls Illumina [4750978] (imputed) 4 bipolar I disorder http://www.ebi.ac.uk/efo/EFO_0009963 GCST011908 Genome-wide genotyping array 2021-06-09 33972514 Pazoki R 2021-05-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33972514 Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes. Liver enzyme levels (alanine transaminase) 437,267 European ancestry individuals 315,572 European ancestry individuals Affymetrix [13995440] (imputed) 150 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90013405 Genome-wide genotyping array 2021-06-09 33972514 Pazoki R 2021-05-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33972514 Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes. Liver enzyme levels (alkaline phosphatase) 437,438 European ancestry individuals 315,572 European ancestry individuals Affymetrix [13995440] (imputed) 290 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90013406 Genome-wide genotyping array 2021-06-09 33972514 Pazoki R 2021-05-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33972514 Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes. Liver enzyme levels (gamma-glutamyl transferase) 437,194 European ancestry individuals 315,572 European ancestry individuals Affymetrix [13995440] (imputed) 200 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90013407 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Depression 65,075 European ancestry cases, 232,552 European ancestry controls NA NR [1198241] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014436 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Systemic lupus erythematosus 624 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90014462 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Ankylosing spondylitis 413 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90014439 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Autoimmune thyroid disease 859 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 autoimmune thyroid disease http://www.ebi.ac.uk/efo/EFO_0006812 GCST90014440 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Autoimmune thyroid disease 607 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 autoimmune thyroid disease http://www.ebi.ac.uk/efo/EFO_0006812 GCST90014441 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Celiac disease 2,364 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90014442 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Celiac disease 1,260 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90014443 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Inflammatory bowel disease 5,105 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90014444 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Inflammatory bowel disease 3,538 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90014445 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Myasthenia gravis 234 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST90014446 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Myasthenia gravis 147 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST90014447 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Multiple sclerosis 1,683 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90014448 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Multiple sclerosis 1,154 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90014449 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Pernicious anemia 1,555 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 pernicious anemia http://www.ebi.ac.uk/efo/EFO_0005576 GCST90014450 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Pernicious anemia 423 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 pernicious anemia http://www.ebi.ac.uk/efo/EFO_0005576 GCST90014451 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Polymyalgia rheumatica 1,627 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90014452 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Polymyalgia rheumatica 898 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90014453 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Psoriatic arthritis 1,107 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90014454 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Psoriatic arthritis 779 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 psoriatic arthritis http://www.ebi.ac.uk/efo/EFO_0003778 GCST90014455 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Psoriasis 5,459 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90014456 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Psoriasis 2,759 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90014457 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Rheumatoid arthritis 6,360 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90014458 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Rheumatoid arthritis 3,451 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90014459 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Sjögren's syndrome 647 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90014460 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Sjögren's syndrome 389 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90014461 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Depression 14,625 European ancestry cases, 232,552 European ancestry controls NA NR [1198241] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014437 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Ankylosing spondylitis 1,344 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90014438 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Systemic lupus erythematosus 362 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90014463 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Type 1 diabetes 2,751 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90014464 Genome-wide genotyping array 2021-07-26 34278373 Glanville KP 2021-06-01 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/34278373 Investigating Pleiotropy Between Depression and Autoimmune Diseases Using the UK Biobank. Type 1 diabetes 2,292 European ancestry cases, 324,074 European ancestry controls NA NR [9940918] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90014465 Genome-wide genotyping array 2021-10-05 34025683 Kanoni S 2021-05-07 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34025683 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD. Hemoglobin levels in non-alcoholic fatty liver disease x mastiha supplementation interaction 35 European or unknown ancestry mastiha exposed individuals, 52 European or unknown ancestry unexposed individuals NA Illumina [10307610] (imputed) 2 hemoglobin measurement, mastiha supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0004509, http://www.ebi.ac.uk/efo/EFO_0600067 GCST012440 Genome-wide genotyping array 2021-10-05 34025683 Kanoni S 2021-05-07 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34025683 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD. Total antioxidant status in non-alcoholic fatty liver disease x mastiha supplementation interaction 35 European or unknown ancestry mastiha exposed individuals, 52 European or unknown ancestry unexposed individuals NA Illumina [10307610] (imputed) 1 antioxidant measurement, mastiha supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0005119, http://www.ebi.ac.uk/efo/EFO_0600067 GCST012439 Genome-wide genotyping array 2021-10-05 34025683 Kanoni S 2021-05-07 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34025683 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD. Interleukin-6 levels in non-alcoholic fatty liver disease x mastiha supplementation interaction 35 European or unknown ancestry mastiha exposed individuals, 52 European or unknown ancestry unexposed individuals NA Illumina [10307610] (imputed) 2 mastiha supplement exposure measurement, interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0600067, http://www.ebi.ac.uk/efo/EFO_0004810 GCST012438 Genome-wide genotyping array 2021-10-05 34025683 Kanoni S 2021-05-07 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34025683 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD. Interleukin-6 gene expression levels in non-alcoholic fatty liver disease x mastiha supplementation interaction 35 European or unknown ancestry mastiha exposed individuals, 52 European or unknown ancestry unexposed individuals NA Illumina [10307610] (imputed) 1 mastiha supplement exposure measurement, interleukin-6 gene expression measurement http://www.ebi.ac.uk/efo/EFO_0600067, http://www.ebi.ac.uk/efo/EFO_0600070 GCST012437 Genome-wide genotyping array 2021-10-05 34025683 Kanoni S 2021-05-07 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34025683 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD. TNF-alpha gene expression levels in non-alcoholic fatty liver disease x mastiha supplementation interaction 35 European or unknown ancestry mastiha exposed individuals, 52 European or unknown ancestry unexposed individuals NA Illumina [10307610] (imputed) 2 mastiha supplement exposure measurement, tumor necrosis factor alpha gene expression measurement http://www.ebi.ac.uk/efo/EFO_0600067, http://www.ebi.ac.uk/efo/EFO_0600069 GCST012436 Genome-wide genotyping array 2021-10-05 34025683 Kanoni S 2021-05-07 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34025683 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD. Interleukin-10 levels in non-alcoholic fatty liver disease x mastiha supplementation interaction 35 European or unknown ancestry mastiha exposed individuals, 51 European or unknown ancestry unexposed individuals NA Illumina [10307610] (imputed) 2 interleukin 10 measurement, mastiha supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0004750, http://www.ebi.ac.uk/efo/EFO_0600067 GCST012435 Genome-wide genotyping array 2021-10-05 34025683 Kanoni S 2021-05-07 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34025683 Nutrigenetic Interactions Might Modulate the Antioxidant and Anti-Inflammatory Status in Mastiha-Supplemented Patients With NAFLD. Glutathione peroxidase in non-alcoholic fatty liver disease x mastiha supplementation interaction 35 European or unknown ancestry mastiha exposed individuals, 52 European or unknown ancestry unexposed individuals NA Illumina [10307610] (imputed) 2 mastiha supplement exposure measurement, blood glutathione peroxidase measurement http://www.ebi.ac.uk/efo/EFO_0600067, http://www.ebi.ac.uk/efo/EFO_0600071 GCST012441 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (sialyl-lacto-N-tetraose c) 395 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 0 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027220 Genome-wide genotyping array 2021-09-10 33831438 Williams JE 2021-04-05 Genomics www.ncbi.nlm.nih.gov/pubmed/33831438 Key genetic variants associated with variation of milk oligosaccharides from diverse human populations. Human milk oligosaccharide concentration (sialyl-lacto-N-tetraose c) in non-secretors 90 European, Sub-Saharan African, Hispanic or unknown ancestry individuals NA Illumina [1128286] 1 breast milk measurement http://www.ebi.ac.uk/efo/EFO_0009092 GCST90027229 Genome-wide genotyping array 2023-03-21 35754308 Kim IY 2022-06-26 J Cosmet Dermatol www.ncbi.nlm.nih.gov/pubmed/35754308 The first broad replication study of SNPs and a pilot genome-wide association study for androgenetic alopecia in Asian populations. Androgenetic alopecia 275 East Asian ancestry cases, 146 East Asian ancestry controls NA Affymetrix [4984245] (imputed) 13 androgenetic alopecia http://www.ebi.ac.uk/efo/EFO_0004191 GCST90257014 Genome-wide genotyping array 2021-10-27 34648798 Seo JY 2021-10-11 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34648798 Genome-wide association study identifies multiple genetic loci for skin color in Korean women. Facial skin colour (CIELAB index L* value) 11,079 Korean ancestry individuals 5,940 Korean ancestry individuals Illumina [5032876] (imputed) 3 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST90020054 Genome-wide genotyping array 2021-10-27 34648798 Seo JY 2021-10-11 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34648798 Genome-wide association study identifies multiple genetic loci for skin color in Korean women. Facial skin colour (CIELAB index a* value) 11,079 Korean ancestry individuals 5,940 Korean ancestry individuals Illumina [5032876] (imputed) 0 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST90020055 Genome-wide genotyping array 2021-10-27 34648798 Seo JY 2021-10-11 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34648798 Genome-wide association study identifies multiple genetic loci for skin color in Korean women. Facial skin colour (CIELAB index b* value) 11,079 Korean ancestry individuals 5,940 Korean ancestry individuals Illumina [5032876] (imputed) 5 facial pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0006942 GCST90020056 Genome-wide genotyping array 2021-10-18 34337532 Fantus RJ 2021-05-25 Eur Urol Open Sci www.ncbi.nlm.nih.gov/pubmed/34337532 Genetic Susceptibility for Low Testosterone in Men and Its Implications in Biology and Screening: Data from the UK Biobank. Low testosterone levels 13,409 European ancestry male cases, 98,267 European ancestry male controls 4,426 European ancestry male cases, 32,800 European ancestry male controls NR [8853336] (imputed) 42 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90026655 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003455 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness lateralorbitofrontal 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003456 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003457 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003458 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003459 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003460 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003461 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003462 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003463 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003464 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003465 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003466 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF atr l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004527 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF atr r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004528 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF cgc l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004529 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF cgc r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004530 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF cgh l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004531 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF cgh r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004532 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF cst l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004533 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF cst r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004534 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF fma 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004535 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF fmi 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004536 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ifo l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004537 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ifo r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004538 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ilf l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004539 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-cingul-Post-ventral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003380 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003381 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-front-inf-Opercular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003382 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-front-inf-Orbital 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003383 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-front-inf-Triangul 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003384 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003385 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003386 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-Ins-lg+S-cent-ins 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003387 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-insular-short 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003388 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-occipital-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003389 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-occipital-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003390 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-oc-temp-lat-fusifor 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003391 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-oc-temp-med-Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003392 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-oc-temp-med-Parahip 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003393 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-orbital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003394 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-pariet-inf-Angular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003395 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-pariet-inf-Supramar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003396 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-parietal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003397 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003398 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003399 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003400 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-rectus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003401 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-subcallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003402 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-temp-sup-G-T-transv 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003403 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-temp-sup-Lateral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003404 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-parietal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003323 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003324 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003325 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003326 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-rectus 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003327 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-subcallosal 21,280 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003328 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-temp-sup-G-T-transv 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003329 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-temp-sup-Lateral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003330 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-temp-sup-Plan-polar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003331 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-temp-sup-Plan-tempo 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003332 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003333 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area G-temporal-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003334 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area Lat-Fis-ant-Horizont 21,277 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003335 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area Lat-Fis-ant-Vertical 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003336 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area Lat-Fis-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003337 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area Pole-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003338 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area Pole-temporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003339 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-calcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003340 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003341 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-cingul-Marginalis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003342 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-circular-insula-ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003343 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-circular-insula-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003344 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-circular-insula-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003345 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-collat-transv-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003346 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-collat-transv-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003347 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ptr r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004470 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD slf l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004471 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD slf r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004472 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD str l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004473 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD str r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004474 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD unc l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004475 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD unc r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004476 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Middle cerebellar peduncle 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004477 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Pontine crossing tract 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004478 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Genu of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004479 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Body of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004480 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Splenium of corpus callosum 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004481 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Fornix 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004482 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Corticospinal tract R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004483 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Corticospinal tract L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004484 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Medial lemniscus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004485 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Medial lemniscus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004486 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Inferior cerebellar peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004487 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Inferior cerebellar peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004488 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior cerebellar peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004489 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior cerebellar peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004490 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Cerebral peduncle R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004491 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Cerebral peduncle L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004492 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Anterior limb of internal capsule R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004493 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Anterior limb of internal capsule L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004494 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-temp-sup-Plan-polar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003405 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-temp-sup-Plan-tempo 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003406 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003407 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-temporal-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003408 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area Lat-Fis-ant-Horizont 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003409 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area Lat-Fis-ant-Vertical 21,269 British ancestry individuals 10,683 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003410 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area Lat-Fis-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003411 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area Pole-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003412 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area Pole-temporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003413 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-calcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003414 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003415 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-cingul-Marginalis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003416 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-circular-insula-ant 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003417 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-circular-insula-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003418 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-circular-insula-sup 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003419 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-collat-transv-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003420 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-collat-transv-post 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003421 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-front-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003422 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003423 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003424 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-interm-prim-Jensen 21,279 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003425 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-intrapariet+P-trans 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003426 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-oc-middle+Lunatus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003427 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-oc-sup+transversal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003428 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-occipital-ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003429 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Superior fronto-occipital fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004445 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Uncinate fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004446 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Uncinate fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004447 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Tapetum R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 1 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004448 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS OD Tapetum L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90004449 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ar l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004450 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ar r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004451 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD atr l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004452 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD atr r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004453 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD cgc l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004454 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD cgc r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004455 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD cgh l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004456 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD cgh r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004457 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD cst l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004458 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD cst r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004459 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD fma 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004460 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD fmi 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004461 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ifo l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004462 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ifo r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004463 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ilf l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004464 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ilf r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004465 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD mcp 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004466 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ml l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004467 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ml r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004468 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX OD ptr l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004469 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile BOLD faces-shapes amygdala 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004565 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median zstat faces-shapes amygdala 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004566 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile zstat faces-shapes amygdala 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004567 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 1) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004568 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 2) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004569 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 3) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004570 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 4) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004571 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 5) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004572 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 6) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004573 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 7) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004574 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 8) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004575 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 9) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004576 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 10) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004577 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 11) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004578 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 12) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004579 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 13) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004580 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 14) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004581 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 15) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004582 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 16) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004583 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 17) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004584 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 18) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004585 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 19) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004586 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 20) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004587 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA25 node 21) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004588 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 1) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004589 Genome-wide genotyping array 2021-03-22 33649486 Hardcastle AJ 2021-03-01 Commun Biol www.ncbi.nlm.nih.gov/pubmed/33649486 A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus. Keratoconus 2,116 European ancestry cases, 24,626 European ancestry controls 1, 389 European ancestry cases, 79,727 European ancestry controls, 759 South Asian ancestry cases, 8,009 South Asian ancestry controls, 405 African ancestry cases, 4,185 African ancestry controls Affymetrix [7701190] (imputed) 36 keratoconus http://purl.obolibrary.org/obo/MONDO_0015486 GCST90013442 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L sup temp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002469 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R sup temp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002470 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L mid temp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002471 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R mid temp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002472 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L mid temp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002473 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R mid temp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002474 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L mid temp gyrus tempocc 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002475 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R mid temp gyrus tempocc 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002476 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L inf temp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002477 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R inf temp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002478 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L inf temp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002479 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R inf temp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002480 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L inf temp gyrus tempocc 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002481 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R inf temp gyrus tempocc 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002482 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L postcent gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002483 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh area S-temporal-transverse 21,280 British ancestry individuals 10,682 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003370 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-frontomargin 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003371 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-occipital-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003372 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003373 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-subcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003374 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-transv-frontopol 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003375 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-cingul-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003376 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-cingul-Mid-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003377 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G+S-cingul-Mid-Post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003378 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area G-cingul-Post-dorsal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003379 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST left hippocampus volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002444 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST right hippocampus volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002445 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST left amygdala volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002446 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST right amygdala volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002447 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST left accumbens volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002448 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST right accumbens volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002449 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST brain stem+4th ventricle volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002450 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L frontal pole 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002451 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R frontal pole 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002452 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L insular cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002453 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R insular cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002454 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L sup front gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002455 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R sup front gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002456 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L mid front gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002457 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R mid front gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002458 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L inf front gyrus parstri 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002459 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R inf front gyrus parstri 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002460 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L inf front gyrus parsop 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002461 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R inf front gyrus parsop 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002462 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L precentral gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002463 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R precentral gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002464 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L temporal pole 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002465 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R temporal pole 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002466 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L sup temp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002467 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R sup temp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002468 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast lateralorbitofrontal 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003803 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003804 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003805 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003806 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003807 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003808 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003809 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003810 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003811 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003812 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003813 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003814 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003815 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003816 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003817 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003818 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003819 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003820 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003821 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003822 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast frontalpole 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003823 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast temporalpole 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003824 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003825 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003826 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast unknown 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003827 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 155) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005008 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 156) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005009 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 157) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005010 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 158) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005011 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 159) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005012 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 160) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005013 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 161) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005014 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 162) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005015 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 163) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005016 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 164) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005017 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 165) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005018 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 166) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005019 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 167) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005020 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 168) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005021 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 169) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005022 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 170) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005023 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 171) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005024 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 172) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005025 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 173) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005026 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 174) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005027 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 175) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005028 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 176) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005029 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 177) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005030 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 178) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005031 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 179) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005032 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 130) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004983 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 131) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004984 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 132) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004985 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 133) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004986 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 134) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004987 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 135) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004988 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 136) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004989 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 137) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004990 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 138) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004991 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 139) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004992 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 140) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004993 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 141) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004994 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 142) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004995 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 143) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004996 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 144) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004997 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 145) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004998 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 146) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004999 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 147) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005000 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 148) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005001 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 149) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005002 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 150) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005003 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 151) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005004 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 152) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005005 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 153) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005006 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 154) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005007 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 544) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005397 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 545) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005398 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 546) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005399 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 547) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005400 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 548) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005401 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 549) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005402 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 550) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005403 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 551) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005404 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 552) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005405 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 553) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005406 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 554) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005407 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 555) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005408 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 556) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005409 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 557) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005410 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 558) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005411 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 559) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005412 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 560) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005413 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 561) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005414 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 562) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005415 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 563) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005416 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 564) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005417 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 565) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005418 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 566) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005419 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 567) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005420 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 667) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005520 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Accumbens-area 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002626 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume VentralDC 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002627 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume vessel 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002628 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume choroid-plexus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002629 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh number HolesBeforeFixing 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002630 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume Cortex 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002631 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh volume CerebralWhiteMatter 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002632 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity ICA-features 2 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006340 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity ICA-features 3 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006341 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity ICA-features 4 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006342 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity ICA-features 5 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006343 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity ICA-features 6 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006344 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC T1-to-standard linear alignment discrepancy 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006345 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC T1-to-standard nonlinear alignment discrepancy 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006346 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC T1-to-standard nonlinear alignment warping 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006347 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC T1 inverse SNR 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006348 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC T1 inverse CNR 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006349 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC T2 FLAIR-to-T1 linear alignment discrepancy 21,386 British ancestry individuals 10,733 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006350 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC dMRI-to-T1 linear alignment discrepancy 21,163 British ancestry individuals 10,640 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006351 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC SWI-to-T1 linear alignment discrepancy 19,545 British ancestry individuals 9,801 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006352 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC rfMRI-to-T1 linear alignment discrepancy 21,091 British ancestry individuals 10,610 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006353 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC tfMRI-to-T1 linear alignment discrepancy 18,420 British ancestry individuals 9,252 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006354 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC rfMRI head motion 21,091 British ancestry individuals 10,610 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006355 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC tfMRI head motion 18,420 British ancestry individuals 9,252 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006356 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC rfMRI inverse tSNR 21,091 British ancestry individuals 10,610 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006357 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC rfMRI cleaned inverse tSNR 21,090 British ancestry individuals 10,609 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006358 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC tfMRI inverse tSNR 18,420 British ancestry individuals 9,252 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006359 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. QC dMRI eddy outlier slices 20,866 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90006360 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 609) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005462 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 610) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005463 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 611) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005464 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 612) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005465 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 613) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005466 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 614) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005467 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 615) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005468 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 616) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005469 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 617) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005470 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 618) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005471 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 619) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005472 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 620) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005473 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 621) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005474 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 622) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005475 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 623) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005476 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 624) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005477 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 625) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005478 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 626) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005479 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 627) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005480 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 628) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005481 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 629) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005482 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 630) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005483 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 656) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005509 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 657) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005510 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 658) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005511 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 659) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005512 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 660) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005513 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 661) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005514 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 662) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005515 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 663) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005516 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 664) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005517 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 665) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005518 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 666) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005519 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 505) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005358 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 506) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005359 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 507) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005360 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 508) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005361 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 509) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005362 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 510) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005363 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 511) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005364 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 512) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005365 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 513) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005366 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 514) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005367 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 515) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005368 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 516) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005369 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 517) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005370 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 518) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005371 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 631) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005484 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 632) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005485 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 633) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005486 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 634) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005487 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 635) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005488 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 636) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005489 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 637) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005490 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 638) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005491 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 639) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005492 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 640) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005493 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 641) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005494 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 642) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005495 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 643) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005496 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 644) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005497 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 645) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005498 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 646) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005499 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 647) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005500 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 648) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005501 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 649) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005502 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 650) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005503 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 651) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005504 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 652) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005505 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 653) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005506 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 654) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005507 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 655) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005508 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 668) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005521 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 669) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005522 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 670) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005523 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 671) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005524 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 672) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005525 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 673) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005526 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 674) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005527 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 675) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005528 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 676) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005529 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 677) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005530 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 678) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005531 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 679) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005532 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 680) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005533 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 681) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005534 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 682) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005535 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 683) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005536 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 684) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005537 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 685) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005538 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 686) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005539 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 687) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005540 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 688) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005541 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 689) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005542 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 690) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005543 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 691) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005544 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 692) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005545 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 519) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005372 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 520) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005373 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 521) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005374 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 522) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005375 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 523) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005376 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 524) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005377 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 525) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005378 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 526) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005379 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 527) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005380 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 528) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005381 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 529) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005382 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 530) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005383 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 531) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005384 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 532) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005385 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 533) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005386 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 534) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005387 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 535) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005388 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 536) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005389 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 537) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005390 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 538) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005391 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 539) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005392 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 540) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005393 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 541) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005394 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 542) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005395 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 543) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005396 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 943) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005796 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 944) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005797 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 945) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005798 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 946) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005799 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 947) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005800 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 948) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005801 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 949) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005802 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 950) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005803 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 951) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005804 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 952) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005805 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 953) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005806 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 954) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005807 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 955) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005808 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 956) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005809 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 957) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005810 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 958) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005811 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 959) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005812 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 960) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005813 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 961) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005814 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 962) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005815 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 963) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005816 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 964) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005817 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 965) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005818 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 966) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005819 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 967) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005820 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 993) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005846 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 994) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005847 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 995) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005848 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 996) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005849 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 997) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005850 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 998) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005851 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 999) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005852 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1000) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005853 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1001) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005854 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 568) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005421 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 569) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005422 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 570) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005423 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 571) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005424 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 572) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005425 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 573) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005426 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 574) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005427 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 575) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005428 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 576) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005429 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 577) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005430 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 578) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005431 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 579) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005432 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 580) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005433 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 581) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005434 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 582) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005435 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 583) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005436 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 968) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005821 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 969) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005822 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 970) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005823 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 971) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005824 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 972) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005825 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 973) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005826 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 974) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005827 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 975) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005828 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 976) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005829 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 977) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005830 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 978) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005831 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 979) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005832 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 980) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005833 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 981) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005834 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 982) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005835 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 983) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005836 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 984) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005837 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 985) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005838 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 986) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005839 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 987) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005840 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 988) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005841 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 989) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005842 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 990) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005843 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 991) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005844 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 992) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005845 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 918) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005771 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 919) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005772 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 920) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005773 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 921) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005774 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 922) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005775 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 923) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005776 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 924) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005777 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 925) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005778 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 926) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005779 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 927) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005780 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 928) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005781 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 929) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005782 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 930) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005783 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 931) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005784 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 932) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005785 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 933) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005786 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 934) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005787 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 935) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005788 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 936) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005789 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 937) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005790 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 938) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005791 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 939) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005792 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 940) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005793 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 941) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005794 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 942) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005795 Genome-wide genotyping array 2021-04-14 33493351 Song Q 2021-01-25 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/33493351 Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus. Systemic lupus erythematosus 512 Han Chinese ancestry cases, 994 Han Chinese ancestry controls NA Illumina [6832025] (imputed) 1 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90014238 Genome-wide genotyping array 2021-04-14 33493351 Song Q 2021-01-25 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/33493351 Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus. Systemic lupus erythematosus 4,734 Chinese ancestry cases, 9,425 Chinese ancestry controls, 4,576 European ancestry cases, 8,039 European ancestry controls NA Illumina [3860730] (imputed) 6 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST011493 Genome-wide genotyping array 2021-04-14 33493351 Song Q 2021-01-25 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/33493351 Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus. Systemic lupus erythematosus 4,576 European ancestry cases, 8,039 European ancestry controls NA Illumina [at least 3860730] 3 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST011492 Genome-wide genotyping array 2021-04-14 33493351 Song Q 2021-01-25 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/33493351 Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus. Systemic lupus erythematosus 4,734 Chinese ancestry cases, 9,425 Chinese ancestry controls NA Illumina [at least 3860730] (imputed) 4 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST011491 Genome-wide genotyping array 2021-06-01 33209044 Ahn Y 2020-11-12 Diabetes Metab Syndr Obes www.ncbi.nlm.nih.gov/pubmed/33209044 Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome. Waist-hip ratio 4,658 Korean ancestry females 5,295 Korean ancestry females Affymetrix [NR] (imputed) 6 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST011775 Genome-wide genotyping array 2021-06-01 33209044 Ahn Y 2020-11-12 Diabetes Metab Syndr Obes www.ncbi.nlm.nih.gov/pubmed/33209044 Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome. Waist circumference 4,658 Korean ancestry females 5,295 Korean ancestry females Affymetrix [NR] (imputed) 2 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST011774 Genome-wide genotyping array 2021-06-01 33209044 Ahn Y 2020-11-12 Diabetes Metab Syndr Obes www.ncbi.nlm.nih.gov/pubmed/33209044 Identification of Genetic Variants for Female Obesity and Evaluation of the Causal Role of Genetically Defined Obesity in Polycystic Ovarian Syndrome. Body mass index 4,658 Korean ancestry females 5,295 Korean ancestry females Affymetrix [NR] (imputed) 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST011776 Genome-wide genotyping array 2021-05-07 33035477 Gisladottir RS 2020-09-25 Curr Biol www.ncbi.nlm.nih.gov/pubmed/33035477 Sequence Variants in TAAR5 and Other Loci Affect Human Odor Perception and Naming. Odorant perception 9,122 Icelandic ancestry individuals 2,204 Icelandic ancestry individuals Illumina [36500000] (imputed) 4 sensory perception of smell http://purl.obolibrary.org/obo/GO_0007608 GCST011623 Genome-wide genotyping array 2021-02-11 33138277 Cismaru AL 2020-10-29 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/33138277 Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations. Metamizole-induced agranulocytosis or neutropenia 45 European ancestry cases, 191 European ancestry controls 41 European ancestry cases, 273 European ancestry controls Illumina [~ 7000000] (imputed) 4 neutropenia, response to metamizole, Drug-induced agranulocytosis http://purl.obolibrary.org/obo/MONDO_0001475, http://www.ebi.ac.uk/efo/EFO_0010971, http://purl.obolibrary.org/obo/HP_0012235 GCST011105 Genome-wide genotyping array 2021-02-11 33138277 Cismaru AL 2020-10-29 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/33138277 Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations. Metamizole-induced agranulocytosis 30 European ancestry cases, 191 European ancestry controls 41 European ancestry cases, 273 European ancestry controls Illumina [~ 7000000] (imputed) 2 response to metamizole, Drug-induced agranulocytosis http://www.ebi.ac.uk/efo/EFO_0010971, http://purl.obolibrary.org/obo/HP_0012235 GCST011106 Genome-wide genotyping array 2021-08-06 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell calcification in response to osteogenic stimuli 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 3 aortic vascular smooth muscle cell calcification measurement http://www.ebi.ac.uk/efo/EFO_0600025 GCST012171 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell migration (difference in area under the curve between PDGF-BB and control media) 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012745 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell migration (difference in rate of initial migration between PDGF-BB and control media) 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012744 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell migration (difference in time to reach maximum migration between PDGF-BB and control media) 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012743 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell proliferation in response to IL-1 beta 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 1 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012746 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell proliferation in response to PDGF-BB 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012742 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell proliferation in response to TGF-beta 1 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012741 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Relative aortic vascular smooth muscle cell proliferation in control medium 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012740 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Relative aortic vascular smooth muscle cell proliferation in response to IL-1 beta 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012739 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Relative aortic vascular smooth muscle cell proliferation in response to PDGF-BB 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012738 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Relative aortic vascular smooth muscle cell proliferation in response to TGF-beta 1 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell proliferation measurement http://www.ebi.ac.uk/efo/EFO_0600026 GCST012737 Genome-wide genotyping array 2022-02-11 33040646 Aherrahrou R 2020-10-12 Circ Res www.ncbi.nlm.nih.gov/pubmed/33040646 Genetic Regulation of Atherosclerosis-Relevant Phenotypes in Human Vascular Smooth Muscle Cells. Aortic vascular smooth muscle cell calcification in response to high inorganic phosphate 69 European ancestry individuals, 64 Hispanic/Latin American individuals, 12 African ancestry individuals, 6 East Asian ancestry individuals NA Illumina [6315002] (imputed) 0 aortic vascular smooth muscle cell calcification measurement http://www.ebi.ac.uk/efo/EFO_0600025 GCST012736 Genome-wide genotyping array 2022-06-01 34096894 Hertz DL 2021-07-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/34096894 Genome-wide association study of letrozole plasma concentrations identifies non-exonic variants that may affect CYP2A6 metabolic activity. Plasma letrozole concentrations in letrozole treated hormone-receptor-positive breast cancer 228 European ancestry individuals NA Illumina [NR] (imputed) 109 response to aromatase inhibitor http://purl.obolibrary.org/obo/GO_0061477 GCST90044900 Genome-wide genotyping array 2021-01-07 33012170 Lanfear DE 2020-10-04 Circ Heart Fail www.ncbi.nlm.nih.gov/pubmed/33012170 Polygenic Score for Beta-Blocker Survival Benefit in European Ancestry Patients with Reduced Ejection Fraction Heart Failure. Beta blocker survival benefit in heart failure with reduced ejection fraction (time to all cause mortality x beta blocker interaction) 248 European ancestry individuals Affymetrix [7000000] (imputed) 12 response to beta blocker, mortality http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0004352 GCST010923 Genome-wide genotyping array 2022-12-01 33201886 Kolin DA 2020-11-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/33201886 Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. COVID-19 846 European ancestry cases, 375,921 European ancestry controls NA Affymetrix [9250219] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST013096 Genome-wide genotyping array 2022-12-01 33201886 Kolin DA 2020-11-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/33201886 Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. COVID-19 66 African ancestry cases, 8,214 African ancestry controls NA Affymetrix [5074382] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST013097 Genome-wide genotyping array 2022-12-01 33201886 Kolin DA 2020-11-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/33201886 Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. COVID-19 56 Asian ancestry cases, 11,960 Asian ancestry controls NA Affymetrix [6029896] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST013098 Genome-wide genotyping array 2022-12-01 33201886 Kolin DA 2020-11-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/33201886 Clinical, regional, and genetic characteristics of Covid-19 patients from UK Biobank. COVID-19 846 European ancestry cases, 375,921 European ancestry controls, 66 African ancestry cases, 8,214 African ancestry controls, 56 Asian ancestry cases, 11,960 Asian ancestry controls NA Affymetrix [9303138] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST013099 Genome-wide genotyping array 2021-03-22 33602968 Skuladottir AT 2021-02-18 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33602968 A meta-analysis uncovers the first sequence variant conferring risk of Bell's palsy. Bell's palsy 4,714 European ancestry cases, 1,011,520 European ancestry controls NA Affymetrix, Illumina [30341632] (imputed) 63 Bell's palsy http://www.ebi.ac.uk/efo/EFO_0007167 GCST011354 Genome-wide genotyping array 2021-06-10 33226468 Foss-Skiftesvik J 2020-11-23 Childs Nerv Syst www.ncbi.nlm.nih.gov/pubmed/33226468 Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci. Pediatric central nervous system tumors (early onset)(pleiotropy) 326 European ancestry cases, 4,320 European ancestry controls NA Illumina [959859] (imputed) 5 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST011831 Genome-wide genotyping array 2021-06-10 33226468 Foss-Skiftesvik J 2020-11-23 Childs Nerv Syst www.ncbi.nlm.nih.gov/pubmed/33226468 Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci. Pediatric central nervous system tumors (late onset)(pleiotropy) 618 European ancestry cases, 4,320 European ancestry controls NA Illumina [959859] (imputed) 2 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST011830 Genome-wide genotyping array 2021-06-10 33226468 Foss-Skiftesvik J 2020-11-23 Childs Nerv Syst www.ncbi.nlm.nih.gov/pubmed/33226468 Genome-wide association study across pediatric central nervous system tumors implicates shared predisposition and points to 1q25.2 (PAPPA2) and 11p12 (LRRC4C) as novel candidate susceptibility loci. Pediatric central nervous system tumors (pleiotropy) 944 European ancestry cases, 4,320 European ancestry controls NA Illumina [959859] (imputed) 4 central nervous system cancer http://www.ebi.ac.uk/efo/EFO_0000326 GCST011832 Genome-wide genotyping array 2021-05-17 33197388 Duckworth A 2020-11-13 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/33197388 Telomere length and risk of idiopathic pulmonary fibrosis and chronic obstructive pulmonary disease: a mendelian randomisation study. Idiopathic pulmonary fibrosis 1,369 European ancestry cases, 435,866 European ancestry controls NA Affymetrix [805426] (imputed) 0 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST90018120 Genome-wide genotyping array 2021-08-24 33730874 Said MA 2021-03-18 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/33730874 Genome-Wide Association Study and Identification of a Protective Missense Variant on Lipoprotein(a) Concentration: Protective Missense Variant on Lipoprotein(a) Concentration. Lipoprotein (a) levels 348,591 European ancestry individuals, 6,000 African ancestry individuals, 9,116 Asian ancestry individuals, 7,505 individuals NR [19000000] (imputed) 39 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST012232 Genome-wide genotyping array 2021-06-04 32964493 Palmer MR 2020-09-22 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32964493 Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network. Carotid artery stenosis 934 British ancestry cases, 408,027 British ancestry controls NA Affymetrix [17981292] (imputed) 2 coronary atherosclerosis measurement http://www.ebi.ac.uk/efo/EFO_0007938 GCST011783 Genome-wide genotyping array 2021-06-04 32964493 Palmer MR 2020-09-22 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/32964493 Loci identified by a genome-wide association study of carotid artery stenosis in the eMERGE network. Carotid artery stenosis 1,705 European ancestry cases, 70 African American cases, 18 cases, 13,198 European ancestry controls, 4,760 African American, Asian, Native Hawaiian or Pacific Islander and unknown ancestry controls 934 British ancestry cases, 408,027 British ancestry controls NR [NR] (imputed) 1 coronary atherosclerosis measurement http://www.ebi.ac.uk/efo/EFO_0007938 GCST011782 Genome-wide genotyping array 2021-01-08 30389748 Emdin CA 2018-11-02 Diabetes www.ncbi.nlm.nih.gov/pubmed/30389748 DNA Sequence Variation in ACVR1C Encoding the Activin Receptor-Like Kinase 7 Influences Body Fat Distribution and Protects Against Type 2 Diabetes. Waist-to-hip ratio adjusted for BMI 335,660 European ancestry individuals, 69,909 individuals 210,088 European ancestry individuals, 14,371 individuals Illumina [614042] 5 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST010926 Exome genotyping array 2021-03-22 33600456 Batai K 2021-02-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33600456 Genetic loci associated with skin pigmentation in African Americans and their effects on vitamin D deficiency. Skin reflectance (Melanin index) 395 African American individuals 681 African American individuals Affymetrix, Illumina [7169107] (imputed) 3 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST011355 Genome-wide genotyping array 2021-04-20 33692975 Buda P 2021-02-22 Front Pediatr www.ncbi.nlm.nih.gov/pubmed/33692975 Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children. Kawasaki disease 119 European ancestry cases, 6,071 European ancestry controls NA Illumina [164395] 16 mucocutaneous lymph node syndrome http://www.ebi.ac.uk/efo/EFO_0004246 GCST90014243 Genome-wide genotyping array 2021-08-27 33740410 Warrier V 2021-03-16 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/33740410 Gene-environment correlations and causal effects of childhood maltreatment on physical and mental health: a genetically informed approach. Childhood maltreatment 185,414 European ancestry individuals NA Affymetrix, Illumina [at least 500527] (imputed) 14 childhood trauma measurement http://www.ebi.ac.uk/efo/EFO_0007979 GCST012253 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Daytime dozing sleeping narcolepsy - Sometimes (UKB data field 1220) 94,586 European ancestry cases, 334,559 European ancestry controls NA Affymetrix, Illumina [546599] 0 narcolepsy without cataplexy, excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0005855, http://www.ebi.ac.uk/efo/EFO_0007875 GCST90077582 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - Need hospital treatment e.g. A&E (UKB data field 20554) (Gene-based burden) 2,509 European ancestry cases, 1,271 European ancestry controls NA Illumina [41575] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90082653 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Contraindications for spirometry (UKB data field 3088) 36,852 European ancestry cases, 392,068 European ancestry controls NA Affymetrix, Illumina [546559] 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90079046 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - Receive help from friends family neighbours (UKB data field 20554) (Gene-based burden) 1,737 European ancestry cases, 2,043 European ancestry controls NA Illumina [41575] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90082656 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seen psychiatrist for nerves anxiety tension or depression (UKB data field 2100) 51,158 European ancestry cases, 377,832 European ancestry controls NA Affymetrix, Illumina [546505] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90078686 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - See anyone from psychiatric or mental health services including liaison services (UKB data field 20554) (Gene-based burden) 2,002 European ancestry cases, 1,778 European ancestry controls NA Illumina [41575] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90082652 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bones in last 5 years (UKB data field 2463) 45,242 European ancestry cases, 383,540 European ancestry controls NA Affymetrix, Illumina [546477] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90078951 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - See own GP (UKB data field 20554) (Gene-based burden) 1,446 European ancestry cases, 2,334 European ancestry controls NA Illumina [41575] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90082655 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Usual walking pace - Brisk pace (UKB data field 924) 176,054 European ancestry cases, 252,201 European ancestry controls NA Affymetrix, Illumina [546001] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079511 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - Use a helpline voluntary organization (UKB data field 20554) (Gene-based burden) 588 European ancestry cases, 3,192 European ancestry controls NA Illumina [41575] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90082654 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Usual walking pace - Slow pace (UKB data field 924) 34,629 European ancestry cases, 393,626 European ancestry controls NA Affymetrix, Illumina [546001] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079509 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat anxiety - Other therapeutic activities such as mindfulness yoga or art classes (UKB data field 20550) (Gene-based burden) 7,965 European ancestry cases, 13,491 European ancestry controls NA Illumina [110085] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90082650 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Usual walking pace - Steady average pace (UKB data field 924) 231,500 European ancestry cases, 196,755 European ancestry controls NA Affymetrix, Illumina [546001] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079510 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat anxiety - Talking therapies such as psychotherapy counselling group therapy or CBT (UKB data field 20550) (Gene-based burden) 17,885 European ancestry cases, 3,571 European ancestry controls NA Illumina [110085] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90082649 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reaction time - Duration to first press of snap button in each round (UKB data field 404) 428,085 European ancestry individuals NA Affymetrix, Illumina [545758] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079143 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat depression - Other therapeutic activities such as mindfulness yoga or art classes (UKB data field 20547) (Gene-based burden) 11,102 European ancestry cases, 24,529 European ancestry controls NA Illumina [130840] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90082637 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seen doctor for nerves anxiety tension or depression (UKB data field 2090) 150,752 European ancestry cases, 277,276 European ancestry controls NA Affymetrix, Illumina [545686] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90078683 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat depression - Talking therapies such as psychotherapy counselling group therapy or CBT (UKB data field 20547) (Gene-based burden) 31,036 European ancestry cases, 4,595 European ancestry controls NA Illumina [130840] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90082636 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean time to correctly identify matches (UKB data field 20023) 427,920 European ancestry individuals NA Affymetrix, Illumina [545597] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078252 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adopted father still alive (UKB data field 3912) (Gene-based burden) 690 European ancestry cases, 3,711 European ancestry controls NA Illumina [47029] 0 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST90083061 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 11 to 15 times a day (UKB data field 943) 87,890 European ancestry cases, 339,312 European ancestry controls NA Affymetrix, Illumina [545053] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079515 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adopted mother still alive (UKB data field 3942) (Gene-based burden) 1,313 European ancestry cases, 3,386 European ancestry controls NA Illumina [49471] 0 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST90083062 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 16 to 20 times a day (UKB data field 943) 41,655 European ancestry cases, 385,547 European ancestry controls NA Affymetrix, Illumina [545053] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079516 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adult asthma (Gene-based burden) 16,937 European ancestry cases, 26,201 European ancestry controls NA Illumina [138029] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90085434 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - More than 20 times a day (UKB data field 943) 31,850 European ancestry cases, 395,352 European ancestry controls NA Affymetrix, Illumina [545053] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079517 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adult asthma vs allergic disease (Gene-based burden) 26,201 European ancestry cases, 280,679 European ancestry controls NA Illumina [183560] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90085435 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - None (UKB data field 943) 40,865 European ancestry cases, 386,337 European ancestry controls NA Affymetrix, Illumina [545053] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079512 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at cancer diagnosis (UKB data field 40008) (Gene-based burden) 78,689 European ancestry individuals NA Illumina [157528] 0 age at diagnosis, cancer http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0004992 GCST90083123 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 1 to 5 times a day (UKB data field 943) 89,153 European ancestry cases, 338,049 European ancestry controls NA Affymetrix, Illumina [545053] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079513 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cancer (UKB data field 2453) 36,403 European ancestry cases, 393,153 European ancestry controls NA Affymetrix, Illumina [547099] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90078950 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severe bleeding 39,650 European ancestry cases, 391,348 European ancestry controls NA Affymetrix, Illumina [548379] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90081527 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry angle left (UKB data field 5111) (Gene-based burden) 101,303 European ancestry individuals NA Illumina [166049] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083275 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time since interview start at which blood pressure screens shown (UKB data field 96) 430,929 European ancestry individuals NA Affymetrix, Illumina [548327] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90079518 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry angle right (UKB data field 5108) (Gene-based burden) 101,582 European ancestry individuals NA Illumina [166161] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083272 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Verbal interview duration (UKB data field 3) 430,929 European ancestry individuals NA Affymetrix, Illumina [548327] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90079078 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level left - doubtful (UKB data field 5155) (Gene-based burden) 2,071 European ancestry cases, 99,232 European ancestry controls NA Illumina [166049] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083295 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching - Number of incorrect matches in round (UKB data field 399) 430,751 European ancestry individuals NA Affymetrix, Illumina [548126] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079077 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level left - high possibility abnormality (UKB data field 5155) (Gene-based burden) 1,659 European ancestry cases, 99,644 European ancestry controls NA Illumina [166049] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083296 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Touchscreen duration (UKB data field 630) 430,751 European ancestry individuals NA Affymetrix, Illumina [548126] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90079491 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level left - normal (UKB data field 5155) (Gene-based burden) 99,415 European ancestry cases, 1,888 European ancestry controls NA Illumina [166049] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083294 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Biometrics duration (UKB data field 4) 430,604 European ancestry individuals NA Affymetrix, Illumina [548039] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90079254 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level right - doubtful (UKB data field 5152) (Gene-based burden) 2,431 European ancestry cases, 99,151 European ancestry controls NA Illumina [166161] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083292 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pace maker (UKB data field 3079) 1,415 European ancestry cases, 429,190 European ancestry controls NA Affymetrix, Illumina [548039] 0 artificial cardiac pacemaker http://www.ebi.ac.uk/efo/EFO_0009719 GCST90079035 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level right - high possibility abnormality (UKB data field 5152) (Gene-based burden) 1,808 European ancestry cases, 99,774 European ancestry controls NA Illumina [166161] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083293 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Handedness chirality laterality - Left handed (UKB data field 1707) 41,056 European ancestry cases, 389,556 European ancestry controls NA Affymetrix, Illumina [548001] 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90077595 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level right - normal (UKB data field 5152) (Gene-based burden) 99,565 European ancestry cases, 2,017 European ancestry controls NA Illumina [166161] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083291 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Handedness chirality laterality - Right handed (UKB data field 1707) 382,514 European ancestry cases, 48,098 European ancestry controls NA Affymetrix, Illumina [548001] 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90077594 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index left (UKB data field 5156) (Gene-based burden) 101,303 European ancestry individuals NA Illumina [166049] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083297 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Handedness chirality laterality - Use both right and left hands equally (UKB data field 1707) 7,455 European ancestry cases, 423,157 European ancestry controls NA Affymetrix, Illumina [548001] 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90077596 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index right (UKB data field 5159) (Gene-based burden) 101,582 European ancestry individuals NA Illumina [166161] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083300 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian left (UKB data field 5097) (Gene-based burden) 89,735 European ancestry individuals NA Illumina [162980] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083260 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hand grip strength right (UKB data field 47) 429,337 European ancestry individuals NA Affymetrix, Illumina [546957] 2 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90079219 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian right (UKB data field 5098) (Gene-based burden) 90,887 European ancestry individuals NA Illumina [163277] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083261 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hand grip strength left (UKB data field 46) 429,288 European ancestry individuals NA Affymetrix, Illumina [546912] 1 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90079216 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Abdominal discomfort pain for 6 months or longer (UKB data field 21027) (Gene-based burden) 43,558 European ancestry cases, 39,720 European ancestry controls NA Illumina [159690] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082682 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever smoked (UKB data field 20160) 263,214 European ancestry cases, 166,087 European ancestry controls NA Affymetrix, Illumina [546860] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90078324 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - About once a month (UKB data field 2110) (Gene-based burden) 24,709 European ancestry cases, 394,103 European ancestry controls NA Illumina [185736] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90082828 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking status - Current (UKB data field 20116) 45,239 European ancestry cases, 384,016 European ancestry controls NA Affymetrix, Illumina [546824] 1 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90078302 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - About once a week (UKB data field 2110) (Gene-based burden) 50,348 European ancestry cases, 368,464 European ancestry controls NA Illumina [185736] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90082829 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking status - Never (UKB data field 20116) 232,790 European ancestry cases, 196,465 European ancestry controls NA Affymetrix, Illumina [546824] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90078300 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - Almost daily (UKB data field 2110) (Gene-based burden) 232,393 European ancestry cases, 186,419 European ancestry controls NA Illumina [185736] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90082831 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking status - Previous (UKB data field 20116) 155,124 European ancestry cases, 274,131 European ancestry controls NA Affymetrix, Illumina [546824] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90078301 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - Never or almost never (UKB data field 2110) (Gene-based burden) 64,936 European ancestry cases, 353,876 European ancestry controls NA Illumina [185736] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90082826 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Excellent (UKB data field 2178) 75,468 European ancestry cases, 353,648 European ancestry controls NA Affymetrix, Illumina [546683] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078846 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - Once every few months (UKB data field 2110) (Gene-based burden) 25,583 European ancestry cases, 393,229 European ancestry controls NA Illumina [185736] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90082827 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Fair (UKB data field 2178) 93,192 European ancestry cases, 335,924 European ancestry controls NA Affymetrix, Illumina [546683] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078848 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to confide - 2 to 4 times a week (UKB data field 2110) (Gene-based burden) 44,658 European ancestry cases, 374,154 European ancestry controls NA Illumina [185736] 0 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST90082830 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Good (UKB data field 2178) 258,685 European ancestry cases, 170,431 European ancestry controls NA Affymetrix, Illumina [546683] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078847 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to walk or cycle unaided for 10 minutes (UKB data field 6017) (Gene-based burden) 77,338 European ancestry cases, 2,894 European ancestry controls NA Illumina [159717] 0 ability to walk or cycle unaided for 10 minutes, self-reported http://www.ebi.ac.uk/efo/EFO_0009822 GCST90083394 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Poor (UKB data field 2178) 19,322 European ancestry cases, 409,794 European ancestry controls NA Affymetrix, Illumina [546683] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078849 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - Above moderate/vigorous recommendation (UKB data field 22035) (Gene-based burden) 190,022 European ancestry cases, 159,371 European ancestry controls NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082841 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Daytime dozing sleeping narcolepsy - Never rarely (UKB data field 1220) 333,750 European ancestry cases, 95,395 European ancestry controls NA Affymetrix, Illumina [546599] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90077581 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - Above moderate/vigorous walking recommendation (UKB data field 22036) (Gene-based burden) 285,477 European ancestry cases, 63,838 European ancestry controls NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082842 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Daytime dozing sleeping narcolepsy - Often (UKB data field 1220) 12,346 European ancestry cases, 416,799 European ancestry controls NA Affymetrix, Illumina [546599] 0 narcolepsy without cataplexy, excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0005855, http://www.ebi.ac.uk/efo/EFO_0007875 GCST90077583 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma-COPD overlap syndrome (Gene-based burden) 14,114 European ancestry cases, 330,697 European ancestry controls NA Illumina [184487] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90085432 Exome-wide sequencing 2021-05-26 34012112 Chiou J 2021-05-19 Nature www.ncbi.nlm.nih.gov/pubmed/34012112 Interpreting type 1 diabetes risk with genetics and single-cell epigenomics. Type 1 diabetes 18,942 European ancestry cases, 501,638 European ancestry controls NA Affymetrix, Illumina [62116689] (imputed) 33 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90014023 Genome-wide genotyping array, Targeted genotyping array [Illumina HumanHap 550 | Illumina Human 1.2M | Illumina Omni1 | Illumina Omni2.5 | Affymetrix 500K | Affymetrix 6.0 | Illumina Human 660W | Illumina Infinium ImmunoArray | Affymetrix UK Biobank Axiom | ThermoFisher Axiom custom] 2021-04-13 31214251 Liu Y 2019-05-31 Front Genet www.ncbi.nlm.nih.gov/pubmed/31214251 Genome-Wide Association Study of Tacrolimus Pharmacokinetics Identifies Novel Single Nucleotide Polymorphisms in the Convalescence and Stabilization Periods of Post-transplant Liver Function. Tacrolimus trough concentration in liver transplant patients 115 Chinese ancestry donors, 115 Chinese ancestry recipients NA Illumina [240000] 0 tacrolimus measurement http://www.ebi.ac.uk/efo/EFO_0008458 GCST011486 Exome genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-oc-temp-lat 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003430 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-oc-temp-med+Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003431 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-orbital-lateral 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003432 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-orbital-med-olfact 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003433 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-orbital-H-Shaped 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003434 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-parieto-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003435 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-pericallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003436 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003437 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-precentral-inf-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003438 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-precentral-sup-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003439 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-suborbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003440 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-subparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003441 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003442 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-temporal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003443 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh area S-temporal-transverse 21,280 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 total cortical area measurement http://www.ebi.ac.uk/efo/EFO_0008381 GCST90003444 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness GlobalMeanThickness 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003445 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003446 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003447 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003448 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003449 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003450 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003451 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003452 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003453 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness isthmuscingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003454 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 47) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004690 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 48) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004691 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 49) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004692 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 50) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004693 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 51) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004694 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 52) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004695 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 53) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004696 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 54) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004697 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 55) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004698 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 56) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004699 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 57) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004700 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 58) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004701 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 59) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004702 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 60) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004703 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 61) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004704 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 62) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004705 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 63) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004706 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 64) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004707 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 65) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004708 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003542 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003543 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003544 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003545 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003546 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003547 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-oc-temp-med-Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003624 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-oc-temp-med-Parahip 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003625 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-orbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003626 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-pariet-inf-Angular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003627 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-pariet-inf-Supramar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003628 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-parietal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003629 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003630 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003631 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003632 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-rectus 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003633 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-subcallosal 21,280 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003634 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-temp-sup-G-T-transv 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003635 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-temp-sup-Lateral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003636 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-temp-sup-Plan-polar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003637 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-temp-sup-Plan-tempo 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003638 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003639 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-temporal-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003640 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness Lat-Fis-ant-Horizont 21,277 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003641 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness Lat-Fis-ant-Vertical 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003642 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 66) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004709 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 67) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004710 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 68) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004711 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 69) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004712 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 70) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004713 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003548 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003549 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003550 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003551 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003552 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003553 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003554 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003555 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003556 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness parsorbitalis 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003557 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003558 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003559 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003560 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003561 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003562 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003563 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness rostralanteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003564 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003565 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003566 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003567 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003568 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003569 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003570 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003571 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003572 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003598 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003599 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003600 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003601 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003602 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-frontomargin 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003603 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-occipital-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003604 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003605 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-subcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003606 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-transv-frontopol 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003607 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-cingul-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003608 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-cingul-Mid-Ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003609 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G+S-cingul-Mid-Post 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003610 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-cingul-Post-dorsal 21,280 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003611 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-cingul-Post-ventral 21,279 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003612 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003613 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-front-inf-Opercular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003614 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-front-inf-Orbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003615 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-front-inf-Triangul 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003616 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003617 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003618 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-Ins-lg+S-cent-ins 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003619 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-insular-short 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003620 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-occipital-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003621 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-occipital-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003622 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003573 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003574 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003575 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003576 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003577 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003578 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003579 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003580 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003581 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003582 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003583 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003584 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003585 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003586 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003587 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003588 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness parstriangularis 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003589 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003590 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003591 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003592 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003593 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003594 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003595 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003596 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas rh thickness superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003597 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 71) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004714 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 72) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004715 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 73) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004716 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 74) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004717 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 75) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004718 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 76) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004719 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 77) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004720 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 78) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004721 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 79) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004722 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 80) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004723 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 81) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004724 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 82) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004725 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 83) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004726 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 84) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004727 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 85) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004728 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 86) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004729 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 87) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004730 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 88) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004731 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 89) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004732 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 90) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004733 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 91) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004734 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 92) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004735 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 93) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004736 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 94) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004737 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 95) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004738 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness G-oc-temp-lat-fusifor 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003623 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels 417,580 European ancestry individuals 80,998 European ancestry individuals, 1,632 individuals NR [8806780] (imputed) 3 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000614 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels 417,580 European ancestry individuals NA NR [8806780] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000615 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels 417,580 European ancestry individuals NA NR [7250403] (imputed) 111 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000616 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels 417,580 European ancestry individuals NA NR [8806780] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000617 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels 496,946 European ancestry individuals NA NR [6912294] (imputed) 150 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000618 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels 177,082 European ancestry individuals NA NR [8806780] (imputed) 24 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000619 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels 162,591 European ancestry individuals NA NR [8806780] (imputed) 10 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000620 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D level variance 318,851 European ancestry individuals NA NR [6098063] (imputed) 25 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000621 Genome-wide genotyping array 2020-10-28 32242144 Revez JA 2020-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32242144 Genome-wide association study identifies 143 loci associated with 25 hydroxyvitamin D concentration. Serum 25-Hydroxyvitamin D levels x season interaction 339,673 European ancestry individuals NA NR [6098063] (imputed) 5 seasonality measurement, vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0006876, http://www.ebi.ac.uk/efo/EFO_0004631 GCST90000622 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Lateral-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003778 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Inf-Lat-Vent 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003779 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Cerebellum-White-Matter 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003780 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Cerebellum-Cortex 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003781 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Thalamus-Proper 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003782 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Caudate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003783 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Putamen 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 13 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003784 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Pallidum 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003785 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Hippocampus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003786 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Amygdala 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003787 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity Accumbens-area 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003788 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity VentralDC 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003789 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity vessel 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003790 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg rh intensity choroid-plexus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003791 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast unknown 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003792 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003793 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003794 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003795 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003796 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003797 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003798 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 10 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003799 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 11 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003800 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast isthmuscingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003801 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg lh intensity-contrast lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003802 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 893) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005746 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 894) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005747 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 895) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005748 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 896) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005749 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 897) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005750 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 898) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005751 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 899) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005752 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 900) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005753 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 901) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005754 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 902) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005755 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 903) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005756 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 904) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005757 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 905) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005758 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 906) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005759 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 907) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005760 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 908) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005761 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 909) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005762 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 910) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005763 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 911) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005764 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 912) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005765 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 913) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005766 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 914) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005767 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 915) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005768 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 916) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005769 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 917) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005770 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 843) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005696 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 844) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005697 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 845) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005698 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 846) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005699 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 847) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005700 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 848) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005701 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 849) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005702 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 850) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005703 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 851) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005704 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 852) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005705 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 853) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005706 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 854) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005707 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 855) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005708 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 856) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005709 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 857) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005710 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 858) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005711 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 859) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005712 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 860) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005713 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 861) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005714 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 862) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005715 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 863) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005716 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 864) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005717 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 865) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005718 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 866) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005719 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 867) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005720 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 868) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005721 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 869) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005722 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 870) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005723 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 871) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005724 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 872) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005725 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 873) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005726 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 874) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005727 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 875) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005728 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 876) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005729 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 877) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005730 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 878) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005731 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 879) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005732 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 880) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005733 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 881) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005734 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 882) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005735 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 883) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005736 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 884) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005737 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 885) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005738 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 886) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005739 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 887) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005740 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 888) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005741 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 889) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005742 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 890) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005743 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 891) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005744 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 892) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005745 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 818) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005671 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 819) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005672 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 820) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005673 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 821) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005674 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 822) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005675 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 823) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005676 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 824) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005677 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 825) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005678 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 826) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005679 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 827) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005680 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 828) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005681 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 829) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005682 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 830) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005683 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 831) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005684 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 832) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005685 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 833) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005686 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 834) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005687 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 835) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005688 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 836) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005689 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 837) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005690 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 838) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005691 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 839) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005692 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 840) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005693 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 841) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005694 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 842) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005695 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD4-CD8- T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001574 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD4+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001575 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Transitional B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001576 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Transitional B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001577 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Transitional B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001578 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD4-CD8- T cell %CD4-CD8- T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001653 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD4-CD8- T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 5 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001654 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD4-CD8- T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001655 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD4-CD8- T cell %CD4-CD8- T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001656 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD4-CD8- T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001657 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ CD4+ T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001658 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ CD4+ T cell %CD4+ T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001659 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ CD4+ T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001660 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD8dim T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001661 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD8dim T cell %CD8dim T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001662 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD8dim T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001663 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA+ CD8dim T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001664 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA+ CD8dim T cell %CD8dim T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001665 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA+ CD8dim T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001666 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA- CD8dim T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001667 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA- CD8dim T cell %CD8dim T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001668 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA- CD8dim T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001669 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ CD8+ T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001670 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ CD8+ T cell %CD8+ T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001671 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ CD8+ T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001672 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD8+ T cell %CD8+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001549 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD8+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001550 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD8+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001551 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD8+ T cell %CD8+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001552 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD8+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001553 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD8+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001554 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD8+ T cell %CD8+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001555 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD8+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001556 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD8+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001557 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD8+ T cell %CD8+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001558 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD8+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001559 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA+ CD8+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001560 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA+ CD8+ T cell %CD8+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001561 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA+ CD8+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001562 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD4-CD8- T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001563 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD4-CD8- T cell %CD4-CD8- T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001564 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD4-CD8- T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001565 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD4-CD8- T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001566 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD4-CD8- T cell %CD4-CD8- T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001567 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD4-CD8- T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001568 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD4-CD8- T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 5 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001569 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD4-CD8- T cell %CD4-CD8- T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001570 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD4-CD8- T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001571 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD4-CD8- T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001572 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD4-CD8- T cell %CD4-CD8- T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001573 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD4+ T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001504 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD4+ T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001505 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD4+ T cell %T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001506 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD45RA+ CD4 not regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001507 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD45RA+ CD4 not regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001508 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD45RA+ CD4 not regulatory T cell %T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001509 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD45RA- CD4 not regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001510 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD45RA- CD4 not regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001511 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD45RA- CD4 not regulatory T cell %T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001512 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001513 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA- CD4+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001534 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA- CD4+ T cell %CD4+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001535 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA- CD4+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001536 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD4+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001537 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD4+ T cell %CD4+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001538 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD4+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001539 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD4+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001540 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive CD4+ T cell %CD4+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001541 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD4+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001542 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD4+ T cell %CD4+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001543 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Effector Memory CD4+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001544 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD4+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001545 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD4+ T cell %CD4+ T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001546 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Terminally Differentiated CD4+ T cell %T cell 3,427 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18349913] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001547 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Central Memory CD8+ T cell Absolute Count 3,395 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332267] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001548 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 regulatory T cell %T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001479 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Resting CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 5 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001480 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Resting CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 5 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001481 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Resting CD4 regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001482 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ resting CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001483 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ resting CD4 regulatory T cell %resting CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001484 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ resting CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001485 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001486 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001487 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated CD4 regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001488 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ activated CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001489 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ activated CD4 regulatory T cell %activated CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001490 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ activated CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001491 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Secreting CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001492 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Secreting CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001493 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Secreting CD4 regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001494 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ secreting CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001495 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ secreting CD4 regulatory T cell %secreting CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001496 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39+ secreting CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001497 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated & resting CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001498 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated & resting CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001499 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated & resting CD4 regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001500 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated & secreting CD4 regulatory T cell Absolute Count 3,405 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18335935] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001501 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated & secreting CD4 regulatory T cell %CD4 regulatory T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 5 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001502 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Activated & secreting CD4 regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001503 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1377) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006230 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1378) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006231 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1379) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006232 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1380) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006233 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1381) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006234 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1382) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006235 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1383) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006236 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1384) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006237 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1385) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006238 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1386) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006239 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1387) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006240 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1388) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006241 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1389) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006242 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1390) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006243 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1391) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006244 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1392) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006245 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1393) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006246 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1394) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006247 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1395) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006248 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1396) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006249 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1397) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006250 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1398) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006251 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1399) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006252 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1400) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006253 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1401) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006254 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1427) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006280 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1428) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006281 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1429) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006282 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1430) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006283 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1431) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006284 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1432) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006285 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1433) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006286 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1434) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006287 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1435) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006288 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1436) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006289 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1437) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006290 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1438) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006291 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1439) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006292 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1440) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006293 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1441) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006294 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1442) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006295 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1443) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006296 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1444) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006297 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1445) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006298 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1446) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006299 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1447) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006300 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1448) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006301 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1449) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006302 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1450) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006303 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1451) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006304 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1402) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006255 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1403) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006256 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1404) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006257 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1405) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006258 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1406) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006259 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1407) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006260 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1408) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006261 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1409) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006262 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1410) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006263 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1411) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006264 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1412) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006265 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1413) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006266 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1414) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006267 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1415) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006268 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1416) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006269 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1417) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006270 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1418) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006271 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1419) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006272 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1420) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006273 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1421) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006274 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1422) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006275 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1423) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006276 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1424) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006277 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1425) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006278 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1426) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006279 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1452) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006305 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1453) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006306 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1454) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006307 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1455) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006308 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1456) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006309 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1457) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006310 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1458) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006311 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1459) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006312 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1460) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006313 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1461) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006314 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1462) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006315 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1463) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006316 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1464) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006317 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1465) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006318 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1466) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006319 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1467) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006320 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1468) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006321 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1469) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006322 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1470) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006323 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1471) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006324 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1472) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006325 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1473) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006326 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1474) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006327 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1475) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006328 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1476) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006329 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1477) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006330 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1478) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006331 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1479) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006332 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1480) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006333 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1481) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006334 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1482) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006335 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1483) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006336 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1484) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006337 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1485) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006338 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity ICA-features 1 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006339 Genome-wide genotyping array 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (apnea hypopnea index) 1,942 African American individuals NA Affymetrix, Illumina [22105437] (imputed) 2 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091014 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (apnea hypopnea index) 8,341 European ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091015 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (apnea hypopnea index) 10,545 European, African American, Hispanic/Latino or East Asian ancestry male individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091016 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin desaturation per event) 10,060 European, African American, Hispanic/Latino or East Asian ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 2 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091017 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin desaturation per event) 7,832 European ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091018 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin desaturation per event) 4,985 European male ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091019 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin desaturation per event) 5,943 European, African American, Hispanic/Latino or East Asian ancestry male individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091020 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin saturation across sleep episode) 21,126 European, African American, Hispanic/Latino or East Asian ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 2 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091021 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin saturation across sleep episode) 8,225 European ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091022 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin saturation across sleep episode) 10,759 Hispanic/Latino individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091023 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (average oxyhemoglobin saturation across sleep episode) 4,167 Hispanic/Latino male ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091024 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (minimum oxyhemoglobin saturation across sleep episode) 21,128 European, African American, Hispanic/Latino or East Asian ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091025 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (minimum oxyhemoglobin saturation across sleep episode) 5,173 European male ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 2 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091026 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (minimum oxyhemoglobin saturation across sleep episode) 10,652 European, African American, Hispanic/Latino or East Asian ancestry female individuals NA Affymetrix, Illumina [22105437] (imputed) 2 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091027 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (minimum oxyhemoglobin saturation across sleep episode) 9,977 Hispanic/Latino individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091028 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (minimum oxyhemoglobin saturation across sleep episode) 10,476 European, African American, Hispanic/Latino or East Asian ancestry male individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091029 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (percentage sleep with oxyhemoglobin saturation less than 90%) 21,244 European, African American, Hispanic/Latino or East Asian ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091030 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (percentage sleep with oxyhemoglobin saturation less than 90%) 1,727 European male ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091031 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (percentage sleep with oxyhemoglobin saturation less than 90%) 10,759 Hispanic/Latino individuals NA Affymetrix, Illumina [22105437] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091032 Genome-wide genotyping array, Genome-wide sequencing 2021-12-13 34446064 Cade BE 2021-08-26 Genome Med www.ncbi.nlm.nih.gov/pubmed/34446064 Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program. Obstructive sleep apnea trait (apnea hypopnea index) 21,244 European, African American, Hispanic/Latino or East Asian ancestry individuals NA Affymetrix, Illumina [22105437] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90091013 Genome-wide genotyping array, Genome-wide sequencing 2022-01-19 34775353 Mousa M 2021-11-11 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/34775353 Genome-wide association study of hospitalized COVID-19 patients in the United Arab Emirates. COVID-19 severity 72 East Asian ancestry cases, 35 East Asian ancestry controls, 81 South Asian ancestry cases, 18 South Asian ancestry controls, 210 European ancestry cases, 92 European ancestry controls, 90 American ancestry cases, 12 American ancestry controls NA Illumina [9175654] (imputed) 8 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90093112 Genome-wide genotyping array 2018-11-12 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Educational attainment (MTAG) 1,311,438 European ancestry individuals NA Affymetrix, Illumina [7100000] (imputed) 1343 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST006571 Genome-wide genotyping array 2018-11-12 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Cognitive performance 257,841 European ancestry individuals NA Affymetrix, Illumina [10100000] (imputed) 217 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST006572 Genome-wide genotyping array 2018-11-12 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Cognitive performance (MTAG) 402,382 European ancestry individuals NA Affymetrix, Illumina [7100000] (imputed) 592 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST006570 Genome-wide genotyping array 2018-11-12 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Self-reported math ability 564,698 European ancestry individuals NA Affymetrix, Illumina [10000000] (imputed) 544 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST006573 Genome-wide genotyping array 2018-11-12 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Self-reported math ability (MTAG) 670,471 European ancestry individuals NA Affymetrix, Illumina [7100000] (imputed) 751 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST006569 Genome-wide genotyping array 2018-11-12 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Highest math class taken 430,445 European ancestry individuals NA Affymetrix, Illumina [10000000] (imputed) 335 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST006574 Genome-wide genotyping array 2018-11-12 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Highest math class taken (MTAG) 811,539 European ancestry individuals NA Affymetrix, Illumina [7100000] (imputed) 1108 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST006568 Genome-wide genotyping array 2018-10-19 30038396 Lee JJ 2018-07-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30038396 Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. Educational attainment (years of education) up to 1,131,881 European ancestry individuals NA Affymetrix, Illumina [10000000] (imputed) 1640 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST006442 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Waist-to-hip ratio adjusted for body mass index 7,272 Hispanic or Latin American females, 5,200 Hispanic or Latin American males up to 12,341 Hispanic or Latin American individuals, 8,913 African American females, 758 African American males, 4,795 European ancestry females, 4,281 European ancestry males Illumina [NR] (imputed) 1 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90086159 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Waist-to-hip ratio adjusted for body mass index 7,272 Hispanic or Latin American females up to 12,341 Hispanic or Latin American females, 8,913 African American females, 4,795 European ancestry females Illumina [NR] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90086160 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Waist-to-hip ratio adjusted for body mass index 5,200 Hispanic or Latin American males up to 12,341 Hispanic or Latin American males, 758 African American males, 4,281 European ancestry males Illumina [NR] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90086161 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Waist circumference adjusted for body mass index 7,272 Hispanic or Latin American females, 5,200 Hispanic or Latin American males up to 12,341 Hispanic or Latin American individuals, 8,913 African American females, 758 African American males, 4,795 European ancestry females, 4,281 European ancestry males Illumina [NR] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90086162 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Waist circumference adjusted for body mass index 7,272 Hispanic or Latin American females up to 12,341 Hispanic or Latin American females, 8,913 African American females 4,795 European ancestry females Illumina [NR] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90086163 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Waist circumference adjusted for body mass index 5,200 Hispanic or Latin American males up to 12,341 Hispanic or Latin American males, 758 African American males, 4,281 European ancestry males Illumina [NR] (imputed) 2 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90086164 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Hip circumference adjusted for BMI 7,272 Hispanic or Latin American females, 5,200 Hispanic or Latin American males up to 12,341 Hispanic or Latin American individuals, 8,913 African American females, 758 African American males, 4,795 European ancestry females, 4,281 European ancestry males Illumina [NR] (imputed) 2 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST90086165 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Hip circumference adjusted for BMI 7,272 Hispanic or Latin American females up to 12,341 Hispanic or Latin American females, 8,913 African American females, 4,795 European ancestry females Illumina [NR] (imputed) 0 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST90086166 Genome-wide genotyping array 2022-01-05 34165540 Justice AE 2021-06-24 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34165540 Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL. Hip circumference adjusted for BMI 5,200 Hispanic or Latin American males up to 12,341 Hispanic or Latin American males, 758 African American males, 4,281 European ancestry males Illumina [NR] (imputed) 3 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST90086167 Genome-wide genotyping array 2022-10-21 33303529 Hernandez-Pacheco N 2020-12-10 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33303529 Genome-wide association study of asthma exacerbations despite inhaled corticosteroids use. Asthma exacerbations in inhaled corticosteroid treatment 2,681 European ancestry individuals 538 European ancestry individuals Affymetrix, Illumina [8100000] (imputed) 0 asthma exacerbation measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0007614, http://purl.obolibrary.org/obo/GO_0031960 GCST013036 Genome-wide genotyping array 2022-10-21 33303529 Hernandez-Pacheco N 2020-12-10 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33303529 Genome-wide association study of asthma exacerbations despite inhaled corticosteroids use. Asthma exacerbations in inhaled corticosteroid treatment 2,681 European ancestry individuals 854 Hispanic individuals Affymetrix, Illumina [8100000] (imputed) 0 asthma exacerbation measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0007614, http://purl.obolibrary.org/obo/GO_0031960 GCST013037 Genome-wide genotyping array 2022-10-21 33303529 Hernandez-Pacheco N 2020-12-10 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33303529 Genome-wide association study of asthma exacerbations despite inhaled corticosteroids use. Asthma exacerbations in inhaled corticosteroid treatment 2,681 European ancestry individuals 493 African American individuals Affymetrix, Illumina [8100000] (imputed) 0 asthma exacerbation measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0007614, http://purl.obolibrary.org/obo/GO_0031960 GCST013038 Genome-wide genotyping array 2022-10-21 33303529 Hernandez-Pacheco N 2020-12-10 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33303529 Genome-wide association study of asthma exacerbations despite inhaled corticosteroids use. Asthma exacerbations in inhaled corticosteroid treatment 2,681 European ancestry individuals 426 Asian ancestry individuals Affymetrix, Illumina [8100000] (imputed) 0 asthma exacerbation measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0007614, http://purl.obolibrary.org/obo/GO_0031960 GCST013039 Genome-wide genotyping array 2022-01-13 34023362 Li B 2021-05-20 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34023362 A Genome-Wide Association Study Finds Variants at 2p21 Associated with Self-Reported Sensitive Skin in the Han Chinese population. Sensitive skin 1,872 Han Chinese ancestry individuals 817 Han Chinese ancestry individuals Affymetrix [530088] (imputed) 1 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90091828 Genome-wide genotyping array 2022-01-13 34023362 Li B 2021-05-20 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34023362 A Genome-Wide Association Study Finds Variants at 2p21 Associated with Self-Reported Sensitive Skin in the Han Chinese population. Sensitive skin 1,192 Han Chinese ancestry females 509 Han Chinese ancestry females Affymetrix [NR] (imputed) 1 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90093095 Genome-wide genotyping array 2022-01-13 34023362 Li B 2021-05-20 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34023362 A Genome-Wide Association Study Finds Variants at 2p21 Associated with Self-Reported Sensitive Skin in the Han Chinese population. Sensitive skin 680 Han Chinese ancestry males 308 Han Chinese ancestry males Affymetrix [NR] (imputed) 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90093096 Genome-wide genotyping array 2022-05-31 35149390 Drogemoller BI 2022-02-08 Biomed Pharmacother www.ncbi.nlm.nih.gov/pubmed/35149390 A pharmacogenomic investigation of the cardiac safety profile of ondansetron in children and pregnant women. Response to ondansetron (change in QTc) 62 Admixed, Admixed American, African, East Asian, European, First Nations, Middle Eastern, South Asian, South East Asian or unknown ancestry cases, 195 Admixed, Admixed American, African, East Asian, European, First Nations, Middle Eastern, South Asian, South East Asian or unknown ancestry controls NA Illumina [NR] (imputed) 4 response to ondansetron, QT interval http://www.ebi.ac.uk/efo/EFO_0020997, http://www.ebi.ac.uk/efo/EFO_0004682 GCST90103785 Genome-wide genotyping array 2022-05-31 35149390 Drogemoller BI 2022-02-08 Biomed Pharmacother www.ncbi.nlm.nih.gov/pubmed/35149390 A pharmacogenomic investigation of the cardiac safety profile of ondansetron in children and pregnant women. Ondansetron-induced QT prolongation 244 Admixed, Admixed American, African, East Asian, European, First Nations, Middle Eastern, South Asian, South East Asian or unknown ancestry individuals NA Illumina [NR] (imputed) 2 response to ondansetron, QT interval http://www.ebi.ac.uk/efo/EFO_0020997, http://www.ebi.ac.uk/efo/EFO_0004682 GCST90103786 Genome-wide genotyping array 2022-01-21 34836030 Park S 2021-10-25 Nutrients www.ncbi.nlm.nih.gov/pubmed/34836030 Interactions between Polygenic Risk Scores, Dietary Pattern, and Menarche Age with the Obesity Risk in a Large Hospital-Based Cohort. Obesity 17,545 Korean ancestry cases, 36,283 Korean ancestry controls 2,756 East Asian ancestry cases, 5,395 East Asian ancestry controls Affymetrix [NR] 1 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90093121 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 27) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004880 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 28) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004881 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 29) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004882 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 30) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004883 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 31) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004884 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 32) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004885 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 33) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004886 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 34) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004887 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 35) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004888 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 36) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004889 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 37) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004890 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 38) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004891 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 39) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004892 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-collat-transv-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003652 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-collat-transv-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003653 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-front-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003654 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003655 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003656 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-interm-prim-Jensen 21,259 British ancestry individuals 10,678 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003657 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-intrapariet+P-trans 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003658 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-oc-middle+Lunatus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003659 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-oc-sup+transversal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003660 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-occipital-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003661 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-oc-temp-lat 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003662 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-oc-temp-med+Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003663 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-orbital-lateral 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003664 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-orbital-med-olfact 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003665 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-orbital-H-Shaped 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 2 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003666 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-parieto-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003667 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-pericallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003668 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003669 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-precentral-inf-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003670 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-precentral-sup-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003671 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-suborbital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003672 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-subparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003673 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003674 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-temporal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003675 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-temporal-transverse 21,280 British ancestry individuals 10,682 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003676 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-frontomargin 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003677 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-occipital-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003678 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003679 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-subcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003680 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-transv-frontopol 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003681 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-cingul-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003682 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-cingul-Mid-Ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003683 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G+S-cingul-Mid-Post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003684 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-cingul-Post-dorsal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003685 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-cingul-Post-ventral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003686 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003687 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-front-inf-Opercular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003688 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-front-inf-Orbital 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003689 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-front-inf-Triangul 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003690 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003691 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003692 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-Ins-lg+S-cent-ins 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003693 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-insular-short 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003694 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-occipital-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003695 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-occipital-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003696 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-oc-temp-lat-fusifor 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003697 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-oc-temp-med-Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003698 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-oc-temp-med-Parahip 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003699 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-orbital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003700 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-pariet-inf-Angular 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003701 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-pariet-inf-Supramar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003702 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-parietal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003703 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003704 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003705 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003706 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-rectus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003707 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-subcallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003708 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-temp-sup-G-T-transv 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003709 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-temp-sup-Lateral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003710 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-temp-sup-Plan-polar 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003711 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-temp-sup-Plan-tempo 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003712 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003713 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness G-temporal-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003714 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness Lat-Fis-ant-Horizont 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003715 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness Lat-Fis-ant-Vertical 21,269 British ancestry individuals 10,683 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003716 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness Lat-Fis-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003717 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness Pole-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003718 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness Pole-temporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003719 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-calcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003720 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003721 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-cingul-Marginalis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003722 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-circular-insula-ant 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003723 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-circular-insula-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003724 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-circular-insula-sup 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003725 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-collat-transv-ant 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003726 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-collat-transv-post 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003727 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-front-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003728 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-front-middle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003729 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-front-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003730 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-interm-prim-Jensen 21,279 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003731 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-intrapariet+P-trans 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003732 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-oc-middle+Lunatus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003733 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-oc-sup+transversal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003734 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-occipital-ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003735 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-oc-temp-lat 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003736 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-oc-temp-med+Lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003737 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-orbital-lateral 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003738 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003828 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003829 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003830 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003831 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003832 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003833 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003834 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 9 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003835 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003836 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003837 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003838 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003839 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003840 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 8 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003841 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003842 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003843 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003844 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003845 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003846 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003847 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. wg rh intensity-contrast postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003848 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 126) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004979 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 127) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004980 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 128) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004981 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 129) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004982 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 205) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005058 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 206) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005059 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R postcent gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002484 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L sup parietal lobule 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002485 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R sup parietal lobule 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002486 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L supramarg gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002487 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R supramarg gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002488 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L supramarg gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002489 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R supramarg gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002490 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L angular gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002491 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R angular gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002492 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L latocc cortex sup 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002493 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R latocc cortex sup 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002494 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L latocc cortex inf 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002495 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R latocc cortex inf 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002496 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L intracalc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002497 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R intracalc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002498 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L front med cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002499 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R front med cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002500 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L juxtapos lobule cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002501 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R juxtapos lobule cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002502 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L subcallosal cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002503 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R subcallosal cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002504 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L paracing gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002505 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R paracing gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002506 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R front operc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002532 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cent operc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002533 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cent operc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002534 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L parietal operc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002535 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R parietal operc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002536 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L planum polare 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002537 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R planum polare 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002538 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L heschl gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002539 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R heschl gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002540 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L planum temporale 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002541 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 207) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005060 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 208) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005061 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 209) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005062 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 210) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005063 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 211) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005064 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 212) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005065 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 213) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005066 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 214) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005067 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 215) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005068 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 216) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005069 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 217) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005070 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 218) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005071 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 219) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005072 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 220) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005073 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 221) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005074 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cing gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002507 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cing gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002508 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cing gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002509 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cing gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002510 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L precun cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002511 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R precun cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002512 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cuneal cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002513 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cuneal cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002514 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L front orb cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002515 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R front orb cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002516 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L parahipp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002517 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R parahipp gyrus ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002518 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L parahipp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002519 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R parahipp gyrus post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002520 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L lingual gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002521 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R lingual gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002522 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L temp fusif cortex ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002523 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R temp fusif cortex ant 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002524 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L temp fusif cortex post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002525 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R temp fusif cortex post 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002526 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L temp occ fusif cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002527 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R temp occ fusif cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002528 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L occ fusif gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002529 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R occ fusif gyrus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002530 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L front operc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002531 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 180) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005033 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 181) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005034 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 182) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005035 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 183) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005036 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 184) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005037 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 185) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005038 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 186) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005039 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 187) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005040 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 188) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005041 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 189) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005042 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 190) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005043 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 191) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005044 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 192) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005045 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 193) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005046 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 194) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005047 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 195) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005048 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 196) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005049 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 197) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005050 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 198) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005051 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 199) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005052 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 200) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005053 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 201) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005054 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 202) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005055 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 203) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005056 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 204) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005057 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 743) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005596 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 744) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005597 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 745) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005598 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 746) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005599 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 747) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005600 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 748) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005601 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 749) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005602 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 750) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005603 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 751) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005604 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 752) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005605 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 753) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005606 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 754) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005607 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 755) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005608 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 756) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005609 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 757) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005610 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 758) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005611 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 759) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005612 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 760) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005613 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 761) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005614 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 762) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005615 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 763) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005616 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 764) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005617 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 765) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005618 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 768) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005621 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 769) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005622 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 770) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005623 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 771) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005624 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 767) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005620 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 793) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005646 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 794) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005647 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 795) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005648 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 796) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005649 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 797) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005650 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 798) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005651 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 799) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005652 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 800) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005653 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 801) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005654 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 802) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005655 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 803) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005656 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 804) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005657 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 805) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005658 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 806) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005659 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 807) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005660 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 808) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005661 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 809) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005662 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 810) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005663 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 811) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005664 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 812) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005665 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 813) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005666 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 814) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005667 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 815) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005668 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 816) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005669 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 817) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005670 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 693) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005546 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 694) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005547 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 695) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005548 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 696) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005549 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 697) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005550 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 698) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005551 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 699) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005552 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 700) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005553 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 701) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005554 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 702) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005555 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 703) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005556 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 704) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005557 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 705) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005558 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 706) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005559 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 707) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005560 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 708) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005561 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 709) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005562 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 710) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005563 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 711) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005564 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 712) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005565 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 713) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005566 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 714) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005567 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 715) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005568 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 716) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005569 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 717) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005570 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 766) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005619 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 772) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005625 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 773) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005626 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 774) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005627 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 775) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005628 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 776) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005629 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 777) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005630 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 778) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005631 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 779) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005632 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 780) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005633 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 781) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005634 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 782) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005635 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 783) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005636 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 784) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005637 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 785) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005638 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 786) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005639 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 787) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005640 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 788) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005641 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 789) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005642 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 790) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005643 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 791) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005644 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 792) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005645 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 718) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005571 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 719) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005572 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 720) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005573 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 721) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005574 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 722) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005575 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 723) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005576 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 724) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005577 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 725) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005578 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 726) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005579 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 727) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005580 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 728) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005581 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 729) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005582 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 730) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005583 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 731) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005584 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 732) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005585 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 733) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005586 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 734) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005587 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 735) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005588 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 736) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005589 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 737) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005590 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 738) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005591 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 739) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005592 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 740) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005593 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 741) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005594 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 742) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005595 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on monocyte 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030638] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001958 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on HLA DR+ CD4+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001959 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001960 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD39+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001961 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD28+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001962 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on myeloid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926605] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001963 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on plasmacytoid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926607] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001964 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on monocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001965 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on granulocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001966 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on CD14+ monocyte 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030638] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001967 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on B cell 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030716] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001968 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on Natural Killer 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001969 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on HLA DR+ Natural Killer 2,971 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17967059] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001970 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on lymphocyte 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001971 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001972 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on CD4+ T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001973 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on CD8+ T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001974 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on HLA DR+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001975 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on Natural Killer T 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001976 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on HLA DR+ CD4+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001977 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. FSC-A on HLA DR+ CD8+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001978 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD16 on CD14- CD16+ monocyte 3,620 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18212540] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001979 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c+ monocyte Absolute Count 3,020 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18122616] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001448 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c+ monocyte %monocyte 3,043 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18133189] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001449 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- monocyte Absolute Count 3,019 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18121986] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001450 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD45RA- CD4 not regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001933 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD45RA+ CD4 not regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001934 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD39+ CD4 regulatory T cell 3,434 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18356566] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001935 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD4 regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001936 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on resting CD4 regulatory T cell 3,434 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357007] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001937 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD39+ resting CD4 regulatory T cell 3,118 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18240965] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001938 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on activated CD4 regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001939 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD39+ activated CD4 regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001940 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on secreting CD4 regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001941 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD39+ secreting CD4 regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001942 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on activated & secreting CD4 regulatory T cell 3,435 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357036] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001943 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD123 on plasmacytoid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926607] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001944 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD123 on CD62L+ plasmacytoid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926607] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001945 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD14+ monocyte 1,634 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999172] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001946 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD33+ HLA DR+ CD14dim 1,577 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16958230] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001947 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD33dim HLA DR+ CD11b+ 1,633 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16998601] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001948 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD33dim HLA DR+ CD11b- 1,634 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999172] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001949 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on Granulocytic Myeloid-Derived Suppressor Cells 1,244 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16551140] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001950 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD66b++ myeloid cell 1,464 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16829425] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001951 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on Monocytic Myeloid-Derived Suppressor Cells 1,569 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16949488] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001952 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD33dim HLA DR- 1,558 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16943119] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001953 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on basophil 1,555 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16937736] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001954 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on Immature Myeloid-Derived Suppressor Cells 1,554 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16934262] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001955 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD33+ HLA DR+ 1,579 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16961928] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001956 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33 on CD33+ HLA DR+ CD14- 1,578 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16961830] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001957 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR7 on naive CD8+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001908 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD14+ monocyte 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030638] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001909 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on B cell 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030716] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001910 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on Natural Killer 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001911 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on HLA DR+ Natural Killer 2,971 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17967059] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001912 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on granulocyte 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030748] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001913 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on lymphocyte 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001914 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001915 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD4+ T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001916 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD8+ T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001917 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on HLA DR+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001918 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on Natural Killer T 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001919 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on HLA DR+ CD4+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001920 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on HLA DR+ CD8+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001921 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001922 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD45RA- CD4 not regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001923 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD28+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001924 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD28+ CD4-CD8- T cell 2,918 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954416] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001925 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on granulocyte 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001926 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001927 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD28+ CD45RA- CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001928 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD28+ CD45RA+ CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001929 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD28- CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001930 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001931 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127 on CD45RA+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001932 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1078) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005931 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1079) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005932 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1080) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005933 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1081) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005934 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1082) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005935 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1083) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005936 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1084) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005937 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1085) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005938 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1086) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005939 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1087) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005940 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1088) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005941 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1089) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005942 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1090) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005943 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1091) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005944 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1092) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005945 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1093) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005946 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1094) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005947 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1095) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005948 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1096) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005949 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1097) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005950 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1098) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005951 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1099) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005952 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1100) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005953 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1101) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005954 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1102) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005955 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1055) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005908 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1056) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005909 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1057) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005910 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1058) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005911 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1059) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005912 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1060) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005913 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1061) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005914 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1062) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005915 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1063) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005916 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1064) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005917 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1065) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005918 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1066) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005919 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 606) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005459 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 607) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005460 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1067) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005920 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1068) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005921 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1069) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005922 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1070) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005923 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1071) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005924 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1072) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005925 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1073) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005926 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1074) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005927 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1075) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005928 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1076) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005929 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1077) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005930 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 584) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005437 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 585) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005438 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 586) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005439 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 587) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005440 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 588) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005441 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 589) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005442 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 590) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005443 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 591) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005444 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 592) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005445 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 593) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005446 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 594) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005447 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 595) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005448 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 596) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005449 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 597) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005450 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 598) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005451 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 599) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005452 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 600) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005453 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 601) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005454 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 602) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005455 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 603) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005456 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 604) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005457 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 605) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005458 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1002) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005855 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1003) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005856 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1004) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005857 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1005) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005858 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1006) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005859 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1007) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005860 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1008) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005861 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1009) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005862 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1010) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005863 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1011) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005864 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1012) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005865 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1013) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005866 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1014) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005867 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1015) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005868 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1016) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005869 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1017) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005870 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1018) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005871 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1019) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005872 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1020) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005873 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1021) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005874 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1022) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005875 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1023) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005876 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1024) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005877 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1025) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005878 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1026) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005879 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1027) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005880 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1028) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005881 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1029) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005882 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1030) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005883 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1031) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005884 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1032) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005885 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1033) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005886 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1034) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005887 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1035) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005888 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1036) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005889 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1037) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005890 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1038) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005891 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1039) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005892 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1040) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005893 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1041) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005894 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1042) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005895 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1043) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005896 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1044) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005897 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1045) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005898 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1046) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005899 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1047) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005900 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1048) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005901 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1049) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005902 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1050) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005903 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1051) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005904 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1052) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005905 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1053) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005906 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1054) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005907 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1103) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005956 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1104) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005957 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1105) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005958 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1106) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005959 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1107) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005960 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1108) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005961 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1109) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005962 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1110) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005963 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1111) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005964 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1112) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005965 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1113) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005966 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1114) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005967 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1115) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005968 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1116) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005969 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1117) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005970 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1118) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005971 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1119) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005972 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1120) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005973 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1121) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005974 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1122) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005975 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1123) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005976 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1124) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005977 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1125) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005978 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1126) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005979 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1127) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005980 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on activated CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002066 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD39+ activated CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002067 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on secreting CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002068 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD39+ secreting CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002069 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on activated & secreting CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002070 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on myeloid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926605] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002071 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on plasmacytoid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926607] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002072 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on monocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002073 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on CD14+ monocyte 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030638] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002074 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on B cell 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030716] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002075 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on Natural Killer 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002076 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on HLA DR+ Natural Killer 2,971 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17967059] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002077 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on granulocyte 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030748] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002078 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on lymphocyte 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002079 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002080 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on CD4+ T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002081 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on CD8+ T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002082 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on HLA DR+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002083 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on Natural Killer T 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002084 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on HLA DR+ CD4+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002085 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. SSC-A on HLA DR+ CD8+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002086 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c on myeloid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926605] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002087 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c on CD62L+ myeloid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926605] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002088 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c on monocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002089 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c on granulocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002090 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11b on CD14+ monocyte 1,635 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999305] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002091 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11b on Granulocytic Myeloid-Derived Suppressor Cells 1,244 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16551140] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002092 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11b on CD66b++ myeloid cell 1,465 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16829575] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002093 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11b on Monocytic Myeloid-Derived Suppressor Cells 1,570 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16949631] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002094 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11b on CD33dim HLA DR- 1,559 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16943254] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002095 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11b on basophil 1,556 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16937871] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002096 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11b on CD33+ HLA DR+ CD14dim 1,578 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16958370] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002097 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA on naive CD4+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002098 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4RA on Terminally Differentiated CD4+ T cell 2,903 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17944758] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002099 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA on naive CD8+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002100 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA on Terminally Differentiated CD8+ T cell 2,911 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945853] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002101 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA on resting CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954460] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002102 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA on CD39+ resting CD4 regulatory T cell 2,650 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17852597] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002103 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on myeloid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926605] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002104 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on plasmacytoid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926607] (imputed) 8 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002105 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926566] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002106 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on Hematopoietic Stem Cell 1,634 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999215] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002107 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD33+ HLA DR+ CD14- 1,579 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16961968] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002108 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD33+ HLA DR+ CD14dim 1,578 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16958370] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002109 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD33dim HLA DR+ CD11b+ 1,634 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16998734] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002110 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD33dim HLA DR+ CD11b- 1,635 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999305] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002111 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD33- HLA DR+ 1,635 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999305] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002112 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on HLA DR+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002113 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on HLA DR+ CD4+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002114 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on HLA DR+ CD8+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002115 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD14+ monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001991 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on CD14+ CD16+ monocyte 3,618 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18213821] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001992 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. PDL-1 on CD14+ CD16- monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001993 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CX3CR1 on CD14- CD16- 3,590 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18203344] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001994 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CX3CR1 on monocyte 3,590 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18203344] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001995 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD66b++ myelod cell 1,465 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16829575] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002048 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CX3CR1 on CD14+ CD16+ monocyte 3,579 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18198165] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001996 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CX3CR1 on CD14+ CD16- monocyte 3,590 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18203344] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001997 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. PDL-1 on CD14+ CD16+ monocyte 3,618 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18213821] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001998 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. PDL-1 on CD14- CD16+ monocyte 3,621 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18212658] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001999 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. PDL-1 on CD14- CD16- 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002000 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD64 on CD14- CD16- 3,622 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18215199] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002001 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. PDL-1 on monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002002 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on CD14- CD16- 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002003 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on CD14+ CD16- monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002004 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD16 on CD14+ CD16+ monocyte 3,617 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18213702] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002005 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD64 on monocyte 3,622 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18215199] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002006 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD14+ CD16+ monocyte 3,618 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18213821] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002007 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002008 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD14- CD16- 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002009 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002010 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD64 on CD14+ CD16+ monocyte 3,611 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18210047] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002011 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CX3CR1 on CD14- CD16+ monocyte 3,582 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18196992] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002012 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on myeloid Dendritic Cell 2,870 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17919786] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002013 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on CD62L+ myeloid Dendritic Cell 2,870 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17919786] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002014 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD80 on granulocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002040 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on lymphocyte 1,635 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999305] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002041 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD33+ HLA DR+ CD14- 1,579 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16961968] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002042 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD33+ HLA DR+ CD14dim 1,578 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16958370] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002043 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD33dim HLA DR+ CD11b- 1,635 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999305] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002044 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD33- HLA DR- 1,635 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999305] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002045 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD33- HLA DR+ 1,635 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999305] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002046 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on Granulocytic Myeloid-Derived Suppressor Cells 1,244 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16551140] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002047 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on Monocytic Myeloid-Derived Suppressor Cells 1,570 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16949631] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002049 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD33dim HLA DR- 1,559 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16943254] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002050 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on basophil 1,556 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16937871] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002051 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on Immature Myeloid-Derived Suppressor Cells 1,555 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16934399] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002052 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45 on CD33+ HLA DR+ 1,580 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16962065] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002053 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on Central Memory CD8+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945467] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002054 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on naive CD8+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002055 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on Effector Memory CD8+ T cell 2,912 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945888] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002056 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on Terminally Differentiated CD8+ T cell 2,911 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945853] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002057 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on CD8+ T cell 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002058 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on Natural Killer T 3,103 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18027570] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002059 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on HLA DR+ CD8+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002060 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD39+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002061 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD28+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002062 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002063 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on resting CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954460] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002064 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD39+ resting CD4 regulatory T cell 2,650 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17852597] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002065 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD28+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001894 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD28+ CD4-CD8- T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954441] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001895 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD28+ CD45RA+ CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001896 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD39+ CD8+ T cell 2,914 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17951426] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001897 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001898 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001899 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on resting CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954460] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001900 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD39+ resting CD4 regulatory T cell 2,650 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17852597] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001901 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on activated CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001902 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86 on myeloid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17923763] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001903 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86 on CD62L+ myeloid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17923763] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001904 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86 on monocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001905 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86 on granulocyte 2,848 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914327] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001906 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR7 on naive CD4+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001907 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD40 on CD14+ CD16- monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001980 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD40 on CD14+ CD16+ monocyte 3,618 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18213821] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001981 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on CD14- CD16+ monocyte 3,621 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18212658] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001982 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14 on CD14+ CD16+ monocyte 3,618 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18213821] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001983 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD14- CD16+ monocyte 3,621 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18212658] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001984 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD40 on monocytes 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001985 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14 on CD14+ CD16- monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001986 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD64 on CD14+ CD16- monocyte 3,622 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18215199] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001987 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on CD14+ CD16- monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18218967] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001988 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD40 on CD14- CD16+ monocyte 3,621 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18212658] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001989 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD64 on CD14- CD16+ monocyte 3,614 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18208887] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001990 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on plasmacytoid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17922630] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002015 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on CD62L+ plasmacytoid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17922630] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002016 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on monocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002017 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CCR2 on granulocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002018 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14 on Monocytic Myeloid-Derived Suppressor Cells 1,570 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16949631] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002019 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14 on CD33+ HLA DR+ CD14dim 1,578 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16958370] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002020 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14 on CD33dim HLA DR+ CD11b+ 1,634 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16998734] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002021 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD4+ T cell 2,912 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945888] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002022 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on Central Memory CD4+ T cell 2,912 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945888] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002023 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on naive CD4+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002024 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on Effector Memory CD4+ T cell 2,912 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945888] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002025 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on Terminally Differentiated CD4+ T cell 2,903 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17944758] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002026 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 on CD45RA+ CD4+ T cell 2,911 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945546] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002027 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on B cell 3,112 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030716] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002028 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39 on CD39+ CD8+ T cell 2,915 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17951463] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002029 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39 on CD39+ activated CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002030 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39 on CD39+ secreting CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002031 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39 on CD39+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002032 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39 on granulocyte 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002033 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD39 on monocyte 2,909 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17952944] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002034 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD80 on myeloid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926466] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002035 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD80 on CD62L+ myeloid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926466] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002036 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD80 on plasmacytoid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926466] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002037 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD80 on CD62L+ plasmacytoid Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926466] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002038 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD80 on monocyte 2,850 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914520] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002039 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on resting CD4 regulatory T cell 2,918 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954415] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001869 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD34 on Hematopoietic Stem Cell 1,634 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16999215] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001870 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001871 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on naive CD8+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001872 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on Effector Memory CD8+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001873 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on Terminally Differentiated CD8+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001874 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on CD4+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001875 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on Central Memory CD4+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001876 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on naive CD4+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001877 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on Effector Memory CD4+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001878 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on Terminally Differentiated CD4+ T cell 1,245 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16405275] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001879 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on CD45RA- CD4+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001880 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on CD8+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001881 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HVEM on Central Memory CD8+ T cell 1,247 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16410374] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001882 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD16-CD56 on Natural Killer T 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001883 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD16-CD56 on Natural Killer 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001884 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD16-CD56 on HLA DR+ Natural Killer 2,971 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17967059] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001885 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD39+ activated CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001886 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on secreting CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001887 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD39+ secreting CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001888 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on activated & secreting CD4 regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001889 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD45RA+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001890 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD45RA- CD4 not regulatory T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001891 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD39+ CD4+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001892 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28 on CD28+ CD45RA- CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001893 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on B cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012789] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002116 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR on HLA DR+ Natural Killer 2,971 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17967059] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002117 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on CD28+ CD45RA- CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002118 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on CD28+ CD45RA+ CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002119 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on CD28- CD8+ T cell 2,920 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954496] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002120 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8 on CD39+ CD8+ T cell 2,915 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17951463] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90002121 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Interleukin-8 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 1 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST90011994 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Vascular endothelial growth factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 5 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST90011995 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Adrenomedullin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 5 adrenomedullin measurement http://www.ebi.ac.uk/efo/EFO_0010909 GCST90011996 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. CD40 ligand levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST90011997 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Growth differentiation factor-15 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90011998 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Placenta growth factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 placenta growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010626 GCST90011999 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. E-selectin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 11 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90012000 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Epidermal growth factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 1 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90012001 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Osteoprotegerin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 9 osteoprotegerin measurement http://www.ebi.ac.uk/efo/EFO_0005918 GCST90012002 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Proto-oncogene tyrosine-protein kinase Src levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 0 proto-oncogene tyrosine-protein kinase Src measurement http://www.ebi.ac.uk/efo/EFO_0010927 GCST90012003 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Interleukin-1-receptor antagonist levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90012004 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Interleukin-6 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90012005 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Cystatin-B levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 cystatin B measurement http://www.ebi.ac.uk/efo/EFO_0010593 GCST90012006 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Monocyte chemoattractant protein-1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 7 monocyte chemotactic protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010596 GCST90012007 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Kallikrein-6 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 kallikrein‐6 measurement http://www.ebi.ac.uk/efo/EFO_0010622 GCST90012008 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Galectin-3 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 12 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90012009 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Proteinase-activated receptor 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 proteinase-activated receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010926 GCST90012010 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. TNF-related apoptosis-inducing ligand levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 TNF-related apoptosis-inducing ligand measurement http://www.ebi.ac.uk/efo/EFO_0008300 GCST90012011 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. kallikrein-11 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90012012 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Angiopoietin-1 receptor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 11 angiopoietin-1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0010600 GCST90012013 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Tissue factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 9 tissue factor measurement http://www.ebi.ac.uk/efo/EFO_0010623 GCST90012014 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Tumor necrosis factor receptor 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 tumor necrosis factor receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010931 GCST90012015 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Platelet-derived growth factor subunit B levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 platelet-derived growth factor BB measurement http://www.ebi.ac.uk/efo/EFO_0008264 GCST90012016 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Interleukin-27 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 15 interleukin-27 measurement http://www.ebi.ac.uk/efo/EFO_0010916 GCST90012017 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Macrophage colony-stimulating factor 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 macrophage colony stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008217 GCST90012018 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Cognitive traits (MTAG) 331,679 British ancestry individuals NA NR [7857346] (imputed) 30 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90011293 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Reaction time 330,024 British ancestry individuals NA NR [7857346] (imputed) 39 reaction time measurement http://www.ebi.ac.uk/efo/EFO_0008393 GCST90011294 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Episodic memory (pairs-matching) 331,679 British ancestry individuals NA NR [7857346] (imputed) 10 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90011295 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Executive function (trail making test B) 78,547 British ancestry individuals NA NR [7857346] (imputed) 7 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90011296 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Information processing speed (symbol digit substitution) 87,741 British ancestry individuals NA NR [7857346] (imputed) 1 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST90011297 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Verbal-numerical reasoning 171,304 British ancestry individuals NA NR [7857346] (imputed) 89 verbal-numerical reasoning measurement http://www.ebi.ac.uk/efo/EFO_0008394 GCST90011298 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Non-verbal reasoning (matrix pattern recognition) 11,356 British ancestry individuals NA NR [7857346] (imputed) 0 reasoning http://www.ebi.ac.uk/efo/EFO_0004350 GCST90011299 Genome-wide genotyping array 2021-06-29 32895543 de la Fuente J 2020-09-07 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/32895543 A general dimension of genetic sharing across diverse cognitive traits inferred from molecular data. Executive function (tower rearranging) 11,263 British ancestry individuals NA NR [7857346] (imputed) 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90011300 Genome-wide genotyping array 2021-02-01 33144438 Kamimura S 2020-11-01 In Vivo www.ncbi.nlm.nih.gov/pubmed/33144438 Association of Genetic Polymorphisms With Hepatitis C Virus-related Liver Cirrhosis in Japan. Cirrhosis 195 Japanese ancestry cases, 1,553 Japanese ancestry controls 753 Japanese ancestry cases, 1,358 Japanese ancestry controls Perlegen [233820] 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST011036 Genome-wide genotyping array 2021-03-24 26942285 Sobota RS 2016-03-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/26942285 A Locus at 5q33.3 Confers Resistance to Tuberculosis in Highly Susceptible Individuals. Tuberculosis susceptibility in HIV infection 267 Sub-Saharan African cases, 314 Sub-Saharan African controls NA Illumina [NR] (imputed) 3 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST011395 Genome-wide genotyping array 2021-01-18 33281188 Suzuki H 2020-12-06 Eur J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/33281188 A genome-wide association study in Japanese identified one variant associated with a preference for a Japanese dietary pattern. Adherence to a Japanese dietary pattern 14,079 Japanese ancestry individuals NA Illumina [7915996] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST010977 Genome-wide genotyping array 2021-06-23 33293427 Emami NC 2020-12-08 Cancer Res www.ncbi.nlm.nih.gov/pubmed/33293427 A large-scale association study detects novel rare variants, risk genes, functional elements, and polygenic architecture of prostate cancer susceptibility. Prostate cancer 14,113 European ancestry cases, 194,140 European ancestry controls NA Affymetrix [at least 232408] (imputed) 48 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011957 Genome-wide genotyping array 2021-04-23 33742053 Wells HRR 2021-03-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33742053 Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank. Tinnitus 91,424 British ancestry individuals NA Affymetrix [9740198] (imputed) 12 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST011541 Genome-wide genotyping array 2021-04-23 33742053 Wells HRR 2021-03-19 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33742053 Genome-wide association study suggests that variation at the RCOR1 locus is associated with tinnitus in UK Biobank. Tinnitus (severest) 87,314 British ancestry individuals NA Affymetrix [9740198] (imputed) 12 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST011540 Genome-wide genotyping array 2021-06-14 33731350 Nandakumar P 2021-03-17 Sci Adv www.ncbi.nlm.nih.gov/pubmed/33731350 Nuclear genome-wide associations with mitochondrial heteroplasmy. Mitochondrial heteroplasmy measurement 982,072 European ancestry individuals NA NR [57525634] (imputed) 20 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST011878 Genome-wide genotyping array 2021-08-25 33756427 Li S 2021-03-20 Environ Int www.ncbi.nlm.nih.gov/pubmed/33756427 Identification of common genetic variants associated with serum concentrations of p, p'-DDE in non-occupational populations in eastern China. DDT metabolite (p,p'-DDE levels) 511 Han Chinese ancestry individuals 1,842 Han Chinese ancestry individuals Illumina [712154] 1 DDT metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007886 GCST012233 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. HDL levels x fish oil supplementation interaction (2df) 67,544 European ancestry individuals 7,284 European ancestry individuals Affymetrix [7954107] (imputed) 5 fish oil supplement exposure measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004612 GCST011927 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. Total cholesterol levels x fish oil supplementation interaction (2df) 73,962 European ancestry individuals 7,283 European ancestry individuals Affymetrix [7953515] (imputed) 2 fish oil supplement exposure measurement, total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004574 GCST011926 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. HDL levels x fish oil supplementation interaction (1df) 67,544 European ancestry individuals 7,284 European ancestry individuals Affymetrix [7954107] (imputed) 1 fish oil supplement exposure measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004612 GCST011930 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. Total cholesterol levels x fish oil supplementation interaction (1df) 73,962 European ancestry individuals 7,283 European ancestry individuals Affymetrix [7953515] (imputed) 1 fish oil supplement exposure measurement, total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004574 GCST011929 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. Triglyceride levels x fish oil supplementation interaction (1df) 73,908 European ancestry individuals 7,284 European ancestry individuals Affymetrix [7953600] (imputed) 2 fish oil supplement exposure measurement, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004530 GCST011928 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. LDL levels x fish oil supplementation interaction (1df) 73,832 European ancestry individuals 7,180 European ancestry individuals Affymetrix [7953137] (imputed) 2 fish oil supplement exposure measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004611 GCST011931 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. Triglyceride levels x fish oil supplementation interaction (2df) 73,908 European ancestry individuals 7,284 European ancestry individuals Affymetrix [7953600] (imputed) 5 fish oil supplement exposure measurement, triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004530 GCST011925 Genome-wide genotyping array 2021-06-17 33760818 Francis M 2021-03-24 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33760818 Genome-wide association study of fish oil supplementation on lipid traits in 81,246 individuals reveals new gene-diet interaction loci. LDL levels x fish oil supplementation interaction (2df) 73,832 European ancestry individuals 7,180 European ancestry individuals Affymetrix [7953137] (imputed) 4 fish oil supplement exposure measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0600007, http://www.ebi.ac.uk/efo/EFO_0004611 GCST011924 Genome-wide genotyping array 2020-10-30 30369944 Balakrishnan P 2018-10-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/30369944 Genetic Variants Related to Cardiometabolic Traits Are Associated to B Cell Function, Insulin Resistance, and Diabetes Among AmeriCan Indians: The Strong Heart Family Study. HOMA-B (corrected for HOMA-IR) 1,892 American Indian ancestry individuals NA Illumina [120975] (imputed) 28 HOMA-B http://www.ebi.ac.uk/efo/EFO_0004469 GCST010724 Targeted genotyping array [Cardio-MetaboChip] 2020-10-09 32869539 de Denus S 2020-09-01 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/32869539 A genetic association study of heart failure: more evidence for the role of BAG3 in idiopathic dilated cardiomyopathy. Heart failure 799 cases, 1,529 controls NA Illumina [Exome array, Agena MassArray] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST010663 Exome genotyping array [Exome array, Agena MassArray] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other eye problems (UKB data field 2227) 68,925 European ancestry cases, 360,799 European ancestry controls NA Affymetrix, Illumina [547154] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90078870 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian angle right (UKB data field 5101) (Gene-based burden) 90,887 European ancestry individuals NA Illumina [163277] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083265 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol drinker status - Previous (UKB data field 20117) 15,969 European ancestry cases, 414,357 European ancestry controls NA Affymetrix, Illumina [547730] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078304 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at menopause - last menstrual period (UKB data field 3581) (Gene-based burden) 140,172 European ancestry individuals NA Illumina [172521] 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90083050 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Brown (UKB data field 1717) 2,065 European ancestry cases, 423,296 European ancestry controls NA Affymetrix, Illumina [543310] 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90077601 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hay fever rhinitis or eczema (age of onset) (UKB data field 3761) (Gene-based burden) 88,602 European ancestry individuals NA Illumina [161367] 0 atopic eczema, age of onset of allergic disease http://www.ebi.ac.uk/efo/EFO_0000274, http://purl.obolibrary.org/obo/OBA_2001017 GCST90083058 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Dark olive (UKB data field 1717) 7,210 European ancestry cases, 418,151 European ancestry controls NA Affymetrix, Illumina [543310] 1 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90077600 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High blood pressure (age of onset) (UKB data field 2966) (Gene-based burden) 108,174 European ancestry individuals NA Illumina [166483] 0 hypertension, age at onset http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90082962 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Fair (UKB data field 1717) 304,034 European ancestry cases, 121,327 European ancestry controls NA Affymetrix, Illumina [543310] 1 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90077598 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hormone replacement therapy last use (age of onset) (UKB data field 3546) (Gene-based burden) 70,090 European ancestry individuals NA Illumina [154213] 0 hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0003961 GCST90083048 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Light olive (UKB data field 1717) 80,996 European ancestry cases, 344,365 European ancestry controls NA Affymetrix, Illumina [543310] 10 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90077599 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hormone replacement therapy use (age of onset) (UKB data field 3536) (Gene-based burden) 83,509 European ancestry individuals NA Illumina [159449] 0 age at onset, hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90083047 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Very fair (UKB data field 1717) 35,374 European ancestry cases, 389,987 European ancestry controls NA Affymetrix, Illumina [543310] 6 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90077597 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oral contraceptive pill use (age of onset) (UKB data field 2794) (Gene-based burden) 184,979 European ancestry individuals NA Illumina [177744] 0 age at onset, contraception http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0009520 GCST90082946 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had bowel cancer screening (UKB data field 2345) 156,242 European ancestry cases, 268,165 European ancestry controls NA Affymetrix, Illumina [542644] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90078936 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking in former smokers (age of onset) (UKB data field 2867) (Gene-based burden) 108,465 European ancestry individuals NA Illumina [166537] 0 smoking status measurement, age at onset http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90082951 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of leg right (UKB data field 23107) 424,024 European ancestry individuals NA Affymetrix, Illumina [542632] 3 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90078910 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses or contact lenses use (age of onset) (UKB data field 2217) (Gene-based burden) 374,837 European ancestry individuals NA Illumina [185092] 0 age at onset, eye measurement http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0004731 GCST90082855 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of leg left (UKB data field 23108) 424,020 European ancestry individuals NA Affymetrix, Illumina [542628] 3 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90078911 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking cessation (age of onset) (UKB data field 2897) (Gene-based burden) 108,447 European ancestry individuals NA Illumina [166515] 0 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST90082955 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of whole body (UKB data field 23106) 424,003 European ancestry individuals NA Affymetrix, Illumina [542627] 2 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90078909 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oral contraceptive pill last use (age of onset) (UKB data field 2804) (Gene-based burden) 169,064 European ancestry individuals NA Illumina [176195] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082947 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of arm left (UKB data field 23110) 424,014 European ancestry individuals NA Affymetrix, Illumina [542624] 2 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90078913 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Airways medication use (Gene-based burden) 36,115 European ancestry cases, 284,643 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90085436 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Impedance of arm right (UKB data field 23109) 423,992 European ancestry individuals NA Affymetrix, Illumina [542602] 2 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90078912 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian angle left (UKB data field 5104) (Gene-based burden) 103,531 European ancestry individuals NA Illumina [166559] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083268 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at first episode of depression (UKB data field 20433) (Gene-based burden) 72,485 European ancestry individuals NA Illumina [155397] 0 unipolar depression, age at onset http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90082435 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 6 to 10 times a day (UKB data field 943) 165,029 European ancestry cases, 262,173 European ancestry controls NA Affymetrix, Illumina [545053] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079514 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at first live birth (UKB data field 2754) (Gene-based burden) 158,740 European ancestry individuals NA Illumina [175025] 0 age at first birth measurement http://www.ebi.ac.uk/efo/EFO_0009101 GCST90082943 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain or discomfort (UKB data field 2335) 71,172 European ancestry cases, 355,555 European ancestry controls NA Affymetrix, Illumina [544531] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90078935 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at last live birth (UKB data field 2764) (Gene-based burden) 158,514 European ancestry individuals NA Illumina [174999] 0 age at last pregnancy measurement http://www.ebi.ac.uk/efo/EFO_0009440 GCST90082944 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Probable type 2 diabetes 17,719 European ancestry cases, 408,623 European ancestry controls NA Affymetrix, Illumina [544298] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90081526 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian angle right (UKB data field 5107) (Gene-based burden) 103,540 European ancestry individuals NA Illumina [166614] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083271 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Wears glasses or contact lenses (UKB data field 2207) 386,786 European ancestry cases, 43,548 European ancestry controls NA Affymetrix, Illumina [547728] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90078860 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian left (UKB data field 5135) (Gene-based burden) 103,531 European ancestry individuals NA Illumina [166559] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083287 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hip circumference (UKB data field 49) 430,214 European ancestry individuals NA Affymetrix, Illumina [547722] 1 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90079253 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian right (UKB data field 5132) (Gene-based burden) 103,540 European ancestry individuals NA Illumina [166614] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083284 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Fairly easy (UKB data field 1170) 222,439 European ancestry cases, 207,750 European ancestry controls NA Affymetrix, Illumina [547618] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90077571 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian angle left (UKB data field 5103) (Gene-based burden) 103,531 European ancestry individuals NA Illumina [166559] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083267 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Not at all easy (UKB data field 1170) 17,267 European ancestry cases, 412,922 European ancestry controls NA Affymetrix, Illumina [547618] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90077569 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian angle right (UKB data field 5100) (Gene-based burden) 103,540 European ancestry individuals NA Illumina [166614] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083264 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Not very easy (UKB data field 1170) 62,083 European ancestry cases, 368,106 European ancestry controls NA Affymetrix, Illumina [547618] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90077570 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian left (UKB data field 5096) (Gene-based burden) 103,531 European ancestry individuals NA Illumina [166559] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083259 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Very easy (UKB data field 1170) 147,370 European ancestry cases, 282,819 European ancestry controls NA Affymetrix, Illumina [547618] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90077572 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian right (UKB data field 5099) (Gene-based burden) 103,540 European ancestry individuals NA Illumina [166614] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083262 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Standing height (UKB data field 50) 430,070 European ancestry individuals NA Affymetrix, Illumina [547612] 26 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90079277 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry angle left (UKB data field 5110) (Gene-based burden) 55,503 European ancestry individuals NA Illumina [148301] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083274 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seated height (UKB data field 51) 430,080 European ancestry individuals NA Affymetrix, Illumina [547605] 4 sitting height measurement http://www.ebi.ac.uk/efo/EFO_0011011 GCST90079330 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry angle right (UKB data field 5109) (Gene-based burden) 56,612 European ancestry individuals NA Illumina [148987] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083273 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sitting height (UKB data field 20015) 430,080 European ancestry individuals NA Affymetrix, Illumina [547605] 7 sitting height measurement http://www.ebi.ac.uk/efo/EFO_0011011 GCST90078245 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alanine aminotransferase levels (UKB data field 30620) (Gene-based burden) 411,932 European ancestry individuals NA Illumina [185667] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90083000 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Loneliness (UKB data field 2020) 79,904 European ancestry cases, 344,503 European ancestry controls NA Affymetrix, Illumina [542464] 0 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST90078372 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Albumin levels (UKB data field 30600) (Gene-based burden) 378,401 European ancestry individuals NA Illumina [185102] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90082998 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change compared with 1 year ago - No, weigh about the same (UKB data field 2306) 249,402 European ancestry cases, 174,786 European ancestry controls NA Affymetrix, Illumina [542415] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078896 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol consumed (UKB data field 100580) (Gene-based burden) 118,267 European ancestry cases, 67,377 European ancestry controls NA Illumina [177616] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90081545 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change compared with 1 year ago - gained weight (UKB data field 2306) 126,122 European ancestry cases, 298,066 European ancestry controls NA Affymetrix, Illumina [542415] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078897 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol drinker status - Current (UKB data field 20117) (Gene-based burden) 401,599 European ancestry cases, 28,727 European ancestry controls NA Illumina [185925] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082291 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change compared with 1 year ago - lost weight (UKB data field 2306) 73,207 European ancestry cases, 350,981 European ancestry controls NA Affymetrix, Illumina [542415] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078898 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol drinker status - Never (UKB data field 20117) (Gene-based burden) 14,617 European ancestry cases, 415,709 European ancestry controls NA Illumina [185925] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082289 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Part of a multiple birth (UKB data field 1777) 9,475 European ancestry cases, 414,637 European ancestry controls NA Affymetrix, Illumina [542402] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90077612 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol drinker status - Previous (UKB data field 20117) (Gene-based burden) 15,969 European ancestry cases, 414,357 European ancestry controls NA Illumina [185925] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082290 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight (UKB data field 23098) 423,702 European ancestry individuals NA Affymetrix, Illumina [542375] 4 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078902 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol liver disease - composite (Gene-based burden) 1,120 European ancestry cases, 376,493 European ancestry controls NA Illumina [185143] 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90085433 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whole body water mass (UKB data field 23102) 423,698 European ancestry individuals 121,642 European ancestry individuals Affymetrix, Illumina [542367] 0 whole body water mass http://www.ebi.ac.uk/efo/EFO_0009805 GCST90078906 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alkaline phosphatase levels (UKB data field 30610) (Gene-based burden) 412,086 European ancestry individuals NA Illumina [185666] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90082999 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Body mass index (UKB data field 23104) 423,694 European ancestry individuals NA Affymetrix, Illumina [542364] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90078907 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergic disease (Gene-based burden) 73,382 European ancestry cases, 280,642 European ancestry controls NA Illumina [184732] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90085437 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Basal metabolic rate (UKB data field 23105) 423,685 European ancestry individuals NA Affymetrix, Illumina [542362] 6 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST90078908 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 10 or more (UKB data field 20403) (Gene-based burden) 3,660 European ancestry cases, 124,233 European ancestry controls NA Illumina [170151] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082387 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whole body fat free mass (UKB data field 23101) 423,664 European ancestry individuals 121,642 European ancestry individuals Affymetrix, Illumina [542347] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90078905 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 1 or 2 (UKB data field 20403) (Gene-based burden) 65,330 European ancestry cases, 62,563 European ancestry controls NA Illumina [170151] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082383 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat percentage right (UKB data field 23111) 423,666 European ancestry individuals NA Affymetrix, Illumina [542342] 1 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90078914 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 3 or 4 (UKB data field 20403) (Gene-based burden) 35,084 European ancestry cases, 92,809 European ancestry controls NA Illumina [170151] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082384 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat mass right (UKB data field 23112) 423,659 European ancestry individuals NA Affymetrix, Illumina [542338] 1 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90078915 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 5 or 6 (UKB data field 20403) (Gene-based burden) 15,507 European ancestry cases, 112,386 European ancestry controls NA Illumina [170151] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082385 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 9 days with pain (UKB data field 21037) (Gene-based burden) 929 European ancestry cases, 43,765 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082738 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had period of mania excitability (UKB data field 20501) 5,876 European ancestry cases, 130,604 European ancestry controls NA Affymetrix, Illumina [236774] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078556 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching - Number of incorrect matches in round (UKB data field 399) (Gene-based burden) 430,751 European ancestry individuals NA Illumina [185946] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083063 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - A little (UKB data field 20460) 8,105 European ancestry cases, 128,310 European ancestry controls NA Affymetrix, Illumina [236678] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078493 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - Number of letters correct in round left (UKB data field 5077) (Gene-based burden) 110,230 European ancestry individuals NA Illumina [168226] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90083252 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - A moderate amount (UKB data field 20460) 36,602 European ancestry cases, 99,813 European ancestry controls NA Affymetrix, Illumina [236678] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078494 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - Number of letters correct in round right (UKB data field 5076) (Gene-based burden) 110,269 European ancestry individuals NA Illumina [168248] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90083251 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - An extreme amount (UKB data field 20460) 17,406 European ancestry cases, 119,009 European ancestry controls NA Affymetrix, Illumina [236678] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078496 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of things worried about during worst period of anxiety - More than one thing (UKB data field 20543) (Gene-based burden) 23,769 European ancestry cases, 18,409 European ancestry controls NA Illumina [136991] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082621 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - Not at all (UKB data field 20460) 2,279 European ancestry cases, 134,136 European ancestry controls NA Affymetrix, Illumina [236678] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078492 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of things worried about during worst period of anxiety - One thing (UKB data field 20543) (Gene-based burden) 18,409 European ancestry cases, 23,769 European ancestry controls NA Illumina [136991] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082620 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - Very much (UKB data field 20460) 72,023 European ancestry cases, 64,392 European ancestry controls NA Affymetrix, Illumina [236678] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078495 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of times self harmed - 1 (UKB data field 20482) (Gene-based burden) 2,892 European ancestry cases, 3,047 European ancestry controls NA Illumina [57310] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90082500 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had period extreme irritability (UKB data field 20502) 35,638 European ancestry cases, 99,747 European ancestry controls NA Affymetrix, Illumina [235211] 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90078557 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of times self harmed - 2 (UKB data field 20482) (Gene-based burden) 1,083 European ancestry cases, 4,856 European ancestry controls NA Illumina [57310] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90082501 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pack years adult smoking as proportion of life span exposed to smoking (UKB data field 20162) 134,156 European ancestry individuals NA Affymetrix, Illumina [232764] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078326 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of times self harmed - 3 or more (UKB data field 20482) (Gene-based burden) 1,964 European ancestry cases, 3,975 European ancestry controls NA Illumina [57310] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90082502 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pack years of smoking (UKB data field 20161) 134,156 European ancestry individuals NA Affymetrix, Illumina [232764] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90078325 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Number of trend entries (UKB data field 6038) (Gene-based burden) 80,512 European ancestry individuals NA Illumina [159836] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083407 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Microalbumin in urine (UKB data field 30500) 133,436 European ancestry individuals NA Affymetrix, Illumina [232072] 2 urinary microalbumin measurement http://www.ebi.ac.uk/efo/EFO_0010967 GCST90079007 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oestradiol levels (UKB data field 30800) (Gene-based burden) 66,773 European ancestry individuals NA Illumina [153771] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90083022 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family history of IBS (UKB data field 21065) 21,959 European ancestry cases, 110,628 European ancestry controls NA Affymetrix, Illumina [231444] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078829 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ongoing addiction to alcohol (UKB data field 20415) (Gene-based burden) 1,387 European ancestry cases, 1,755 European ancestry controls NA Illumina [35092] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90082417 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever felt worried tense or anxious for most of a month or longer (UKB data field 20421) 34,789 European ancestry cases, 95,747 European ancestry controls NA Affymetrix, Illumina [228201] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078439 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ongoing behavioural or miscellanous addiction (UKB data field 20432) (Gene-based burden) 916 European ancestry cases, 1,005 European ancestry controls NA Illumina [23488] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90082434 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - furosemide (Gene-based burden) 3,399 European ancestry cases, 317,359 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082122 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm left started wearing glasses contacts before 40 47,125 European ancestry individuals NA Affymetrix, Illumina [95216] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081479 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fybogel mebeverine sachet (Gene-based burden) 665 European ancestry cases, 320,093 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082014 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm right started wearing glasses contacts before 40 47,122 European ancestry individuals NA Affymetrix, Illumina [95141] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081481 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fybogel orange s/f granules (Gene-based burden) 947 European ancestry cases, 319,811 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082200 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time since last menstrual period (UKB data field 3700) 46,881 European ancestry individuals NA Affymetrix, Illumina [94045] 0 menstrual cycle measurement http://www.ebi.ac.uk/efo/EFO_0007786 GCST90079068 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gabapentin (Gene-based burden) 2,240 European ancestry cases, 318,518 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082054 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H71: Cholesteatoma of middle ear 502 European ancestry cases, 387,301 European ancestry controls NA Affymetrix, Illumina [91086] 0 cholesteatoma of middle ear http://www.ebi.ac.uk/efo/EFO_1000678 GCST90079937 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - garlic product (Gene-based burden) 5,915 European ancestry cases, 314,843 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082132 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Ankle (UKB data field 6151) 6,598 European ancestry cases, 38,595 European ancestry controls NA Affymetrix, Illumina [91068] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079446 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gaviscon liquid (Gene-based burden) 2,498 European ancestry cases, 318,260 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082015 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Arm (UKB data field 6151) 4,818 European ancestry cases, 40,375 European ancestry controls NA Affymetrix, Illumina [91068] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079451 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ginkgo forte tablet (Gene-based burden) 2,502 European ancestry cases, 318,256 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082133 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Hip (UKB data field 6151) 823 European ancestry cases, 44,370 European ancestry controls NA Affymetrix, Illumina [91068] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079448 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ginseng product (Gene-based burden) 633 European ancestry cases, 320,125 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082134 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Leg (UKB data field 6151) 3,016 European ancestry cases, 42,177 European ancestry controls NA Affymetrix, Illumina [91068] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079447 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gliclazide (Gene-based burden) 3,820 European ancestry cases, 316,938 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082058 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Other bones (UKB data field 6151) 24,623 European ancestry cases, 20,570 European ancestry controls NA Affymetrix, Illumina [91068] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079452 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - glucosamine product (Gene-based burden) 29,647 European ancestry cases, 291,111 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082209 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Spine (UKB data field 6151) 1,130 European ancestry cases, 44,063 European ancestry controls NA Affymetrix, Illumina [91068] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079449 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 70 (UKB data field 4990) 31,252 European ancestry cases, 105,139 European ancestry controls NA Affymetrix, Illumina [236885] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079250 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 7 days with pain (UKB data field 21037) (Gene-based burden) 1,828 European ancestry cases, 42,866 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082736 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 71 (UKB data field 4990) 739 European ancestry cases, 135,652 European ancestry controls NA Affymetrix, Illumina [236885] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079251 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 8 days with pain (UKB data field 21037) (Gene-based burden) 1,632 European ancestry cases, 43,062 European ancestry controls NA Illumina [139300] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082737 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 72 (UKB data field 4990) 885 European ancestry cases, 135,506 European ancestry controls NA Affymetrix, Illumina [236885] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079252 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Townsend deprivation index at recruitment (UKB data field 189) 430,494 European ancestry individuals NA Affymetrix, Illumina [547908] 0 Townsend deprivation index http://www.ebi.ac.uk/efo/EFO_0009711 GCST90077617 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power angle left (UKB data field 5112) (Gene-based burden) 103,515 European ancestry individuals NA Illumina [166557] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083276 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Current tobacco smoking on most or all days (UKB data field 1239) 33,523 European ancestry cases, 396,975 European ancestry controls NA Affymetrix, Illumina [547903] 1 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90077584 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power angle right (UKB data field 5115) (Gene-based burden) 103,530 European ancestry individuals NA Illumina [166611] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083279 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeplessness insomnia - Never rarely (UKB data field 1200) 107,304 European ancestry cases, 323,123 European ancestry controls NA Affymetrix, Illumina [547818] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90077577 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power left (UKB data field 5119) (Gene-based burden) 103,531 European ancestry individuals NA Illumina [166559] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083283 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeplessness insomnia - Sometimes (UKB data field 1200) 213,925 European ancestry cases, 216,502 European ancestry controls NA Affymetrix, Illumina [547818] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90077578 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power right (UKB data field 5116) (Gene-based burden) 103,540 European ancestry individuals NA Illumina [166614] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083280 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeplessness insomnia - Usually (UKB data field 1200) 130,457 European ancestry cases, 299,970 European ancestry controls NA Affymetrix, Illumina [547818] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90077579 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index for irregular astigmatism level right - doubtful (UKB data field 5164) (Gene-based burden) 4,583 European ancestry cases, 97,024 European ancestry controls NA Illumina [166173] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083306 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Waist circumference (UKB data field 48) 430,261 European ancestry individuals NA Affymetrix, Illumina [547767] 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90079228 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index for irregular astigmatism level right - high possibility abnormality (UKB data field 5164) (Gene-based burden) 4,456 European ancestry cases, 97,151 European ancestry controls NA Illumina [166173] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083307 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Always (UKB data field 2267) 96,475 European ancestry cases, 333,934 European ancestry controls NA Affymetrix, Illumina [547745] 2 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90078882 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index for irregular astigmatism level right - normal (UKB data field 5164) (Gene-based burden) 97,932 European ancestry cases, 3,675 European ancestry controls NA Illumina [166173] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083305 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Do not go out in sunshine (UKB data field 2267) 2,503 European ancestry cases, 427,906 European ancestry controls NA Affymetrix, Illumina [547745] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90078883 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index irregular astigmatism level left - doubtful (UKB data field 5149) (Gene-based burden) 4,465 European ancestry cases, 96,853 European ancestry controls NA Illumina [166055] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083289 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Most of the time (UKB data field 2267) 166,473 European ancestry cases, 263,936 European ancestry controls NA Affymetrix, Illumina [547745] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90078881 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index irregular astigmatism level left - high possibility abnormality (UKB data field 5149) (Gene-based burden) 4,393 European ancestry cases, 96,925 European ancestry controls NA Illumina [166055] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083290 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Never rarely (UKB data field 2267) 38,347 European ancestry cases, 392,062 European ancestry controls NA Affymetrix, Illumina [547745] 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90078879 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index irregular astigmatism level left - normal (UKB data field 5149) (Gene-based burden) 97,566 European ancestry cases, 3,752 European ancestry controls NA Illumina [166055] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083288 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Use of sun UV protection - Sometimes (UKB data field 2267) 150,448 European ancestry cases, 279,961 European ancestry controls NA Affymetrix, Illumina [547745] 1 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90078880 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index left (UKB data field 5163) (Gene-based burden) 101,318 European ancestry individuals NA Illumina [166055] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083304 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol drinker status - Current (UKB data field 20117) 401,599 European ancestry cases, 28,727 European ancestry controls NA Affymetrix, Illumina [547730] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078305 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index right (UKB data field 5160) (Gene-based burden) 101,607 European ancestry individuals NA Illumina [166173] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083301 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol drinker status - Never (UKB data field 20117) 14,617 European ancestry cases, 415,709 European ancestry controls NA Affymetrix, Illumina [547730] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078303 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry index left (UKB data field 5157) (Gene-based burden) 55,503 European ancestry individuals NA Illumina [148301] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083298 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Blonde (UKB data field 1747) 48,595 European ancestry cases, 381,384 European ancestry controls NA Affymetrix, Illumina [547490] 7 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90077606 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry index right (UKB data field 5158) (Gene-based burden) 56,612 European ancestry individuals NA Illumina [148987] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083299 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Dark brown (UKB data field 1747) 164,398 European ancestry cases, 265,581 European ancestry controls NA Affymetrix, Illumina [547490] 11 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90077609 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power angle left (UKB data field 5113) (Gene-based burden) 89,706 European ancestry individuals NA Illumina [162967] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083277 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Light brown (UKB data field 1747) 175,455 European ancestry cases, 254,524 European ancestry controls NA Affymetrix, Illumina [547490] 1 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90077608 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power angle right (UKB data field 5114) (Gene-based burden) 90,862 European ancestry individuals NA Illumina [163273] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083278 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Other (UKB data field 1747) 5,564 European ancestry cases, 424,415 European ancestry controls NA Affymetrix, Illumina [547490] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90077611 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power left (UKB data field 5118) (Gene-based burden) 89,735 European ancestry individuals NA Illumina [162980] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083282 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Red (UKB data field 1747) 19,553 European ancestry cases, 410,426 European ancestry controls NA Affymetrix, Illumina [547490] 7 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90077607 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power right (UKB data field 5117) (Gene-based burden) 90,887 European ancestry individuals NA Illumina [163277] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083281 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Black (UKB data field 1747) 20,623 European ancestry cases, 409,356 European ancestry controls NA Affymetrix, Illumina [547480] 3 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90077610 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm regularity index left (UKB data field 5162) (Gene-based burden) 55,532 European ancestry individuals NA Illumina [148320] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083303 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight (UKB data field 21002) 429,785 European ancestry individuals NA Affymetrix, Illumina [547405] 4 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078685 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm regularity index right (UKB data field 5161) (Gene-based burden) 56,694 European ancestry individuals NA Illumina [149030] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083302 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Body mass index (UKB data field 21001) 429,633 European ancestry individuals 121,642 European ancestry individuals Affymetrix, Illumina [547270] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90078684 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian angle left (UKB data field 5105) (Gene-based burden) 89,735 European ancestry individuals NA Illumina [162980] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083269 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Falls in the last year - More than one fall (UKB data field 2296) 30,374 European ancestry cases, 399,492 European ancestry controls NA Affymetrix, Illumina [547266] 0 fall http://www.ebi.ac.uk/efo/EFO_0009631 GCST90078885 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian angle right (UKB data field 5106) (Gene-based burden) 90,887 European ancestry individuals NA Illumina [163277] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083270 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Falls in the last year - Only one fall (UKB data field 2296) 62,653 European ancestry cases, 367,213 European ancestry controls NA Affymetrix, Illumina [547266] 0 fall http://www.ebi.ac.uk/efo/EFO_0009631 GCST90078884 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian left (UKB data field 5134) (Gene-based burden) 89,735 European ancestry individuals NA Illumina [162980] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083286 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetes mellitus (UKB data field 2443) 22,058 European ancestry cases, 407,681 European ancestry controls NA Affymetrix, Illumina [547219] 1 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90078949 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian right (UKB data field 5133) (Gene-based burden) 90,887 European ancestry individuals NA Illumina [163277] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083285 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overweight 287,014 European ancestry cases, 142,553 European ancestry controls NA Affymetrix, Illumina [547214] 0 overweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005935 GCST90081523 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian angle left (UKB data field 5102) (Gene-based burden) 89,735 European ancestry individuals NA Illumina [162980] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083266 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat percentage left (UKB data field 23115) 423,643 European ancestry individuals NA Affymetrix, Illumina [542318] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90078918 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anisometropia - started wearing glasses or contacts before 40 (Gene-based burden) 48,482 European ancestry individuals NA Illumina [143543] 0 Anisometropia http://purl.obolibrary.org/obo/HP_0012803 GCST90085440 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat mass left (UKB data field 23116) 423,640 European ancestry individuals NA Affymetrix, Illumina [542312] 1 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90078919 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankle spacing width (UKB data field 3143) (Gene-based burden) 246,319 European ancestry individuals NA Illumina [181011] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90083034 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat free mass left (UKB data field 23117) 423,624 European ancestry individuals NA Affymetrix, Illumina [542295] 5 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90078920 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankle spacing width left (UKB data field 4100) (Gene-based burden) 166,283 European ancestry individuals NA Illumina [176191] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90083134 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg predicted mass left (UKB data field 23118) 423,618 European ancestry individuals NA Affymetrix, Illumina [542292] 5 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90078921 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fluoxetine (Gene-based burden) 5,309 European ancestry cases, 315,449 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082074 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent right - started wearing glasses contacts before 40 48,976 European ancestry individuals NA Affymetrix, Illumina [98459] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081513 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fluticasone (Gene-based burden) 2,123 European ancestry cases, 318,635 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082107 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent left - started wearing glasses contacts before 40 48,821 European ancestry individuals NA Affymetrix, Illumina [98207] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081511 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - folic acid product (Gene-based burden) 3,838 European ancestry cases, 316,920 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082041 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anisometropia - started wearing glasses or contacts before 40 48,482 European ancestry individuals NA Affymetrix, Illumina [97567] 0 Anisometropia http://purl.obolibrary.org/obo/HP_0012803 GCST90081454 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - food supplement plant herbal extract (Gene-based burden) 1,616 European ancestry cases, 319,142 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082224 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean spherical equivalent - started wearing glasses or contacts before 40 48,482 European ancestry individuals NA Affymetrix, Illumina [97567] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081498 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fosamax (Gene-based burden) 532 European ancestry cases, 320,226 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082194 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Refractive astigmatism - started wearing glasses contacts before 40 48,482 European ancestry individuals NA Affymetrix, Illumina [97567] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90081507 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - frusemide (Gene-based burden) 776 European ancestry cases, 319,982 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082022 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal power - started wearing glasses or contacts before 40 47,125 European ancestry individuals NA Affymetrix, Illumina [95216] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081538 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Miserableness (UKB data field 1930) 186,446 European ancestry cases, 237,632 European ancestry controls NA Affymetrix, Illumina [542325] 0 feeling miserable measurement http://www.ebi.ac.uk/efo/EFO_0009598 GCST90077619 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 7, 8 or 9 (UKB data field 20403) (Gene-based burden) 8,312 European ancestry cases, 119,581 European ancestry controls NA Illumina [170151] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082386 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg fat free mass right (UKB data field 23113) 423,650 European ancestry individuals NA Affymetrix, Illumina [542324] 4 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90078916 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anisometropia (Gene-based burden) 106,495 European ancestry individuals NA Illumina [167325] 0 Anisometropia http://purl.obolibrary.org/obo/HP_0012803 GCST90085439 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg predicted mass right (UKB data field 23114) 423,649 European ancestry individuals NA Affymetrix, Illumina [542323] 4 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90078917 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anisometropia (first instance) (Gene-based burden) 93,186 European ancestry individuals NA Illumina [164300] 0 Anisometropia http://purl.obolibrary.org/obo/HP_0012803 GCST90085438 Exome-wide sequencing 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Superior fronto-occipital fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004520 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Uncinate fasciculus R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004521 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Uncinate fasciculus L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004522 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Tapetum R 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004523 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI TBSS ISOVF Tapetum L 20,859 British ancestry individuals 10,496 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004524 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ar l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004525 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ar r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004526 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX peripheral grey normalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002426 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX peripheral grey unnormalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002427 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX CSF normalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002428 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX CSF unnormalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002429 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX grey normalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002430 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX grey unnormalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002431 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX white normalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002432 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX white unnormalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002433 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX brain-normalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002434 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 SIENAX brain-unnormalised volume 22,138 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002435 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST left thalamus volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002436 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST right thalamus volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002437 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST left caudate volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002438 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST right caudate volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002439 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST left putamen volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002440 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST right putamen volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002441 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST left pallidum volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002442 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FIRST right pallidum volume 22,128 British ancestry individuals 11,083 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002443 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ilf r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004540 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF mcp 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004541 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ml l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004542 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ml r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004543 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ptr l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004544 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF ptr r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004545 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF slf l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 6 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004546 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF slf r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004547 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF str l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004548 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF str r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004549 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF unc l 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004550 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP dMRI ProbtrackX ISOVF unc r 20,859 British ancestry individuals 10,495 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004551 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median BOLD shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004552 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile BOLD shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004553 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median zstat shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004554 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile zstat shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004555 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median BOLD faces 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004556 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile BOLD faces 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004557 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median zstat faces 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004558 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile zstat faces 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004559 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median BOLD faces-shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004560 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile BOLD faces-shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004561 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median zstat faces-shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004562 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI 90th-percentile zstat faces-shapes 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004563 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP tfMRI median BOLD faces-shapes amygdala 18,412 British ancestry individuals 9,251 British ancestry individuals Affymetrix [17103079] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90004564 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-DKTatlas lh thickness caudalanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003541 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 28) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004616 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 29) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004617 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 30) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004618 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 31) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004619 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 32) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004620 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 33) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004621 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 34) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004622 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 35) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004623 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 36) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004624 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 37) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004625 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 38) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004626 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 39) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004627 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 40) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004628 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 41) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004629 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 42) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004630 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 43) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004631 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 44) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004632 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 45) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004633 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 46) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004634 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 47) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004635 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 48) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004636 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 49) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004637 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 50) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004638 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 51) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004639 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 2) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004590 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 3) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004591 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 4) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004592 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 5) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004593 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 6) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004594 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 7) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004595 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 8) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004596 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 9) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004597 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 10) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004598 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 11) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004599 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 12) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004600 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 13) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004601 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 14) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004602 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 15) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004603 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 16) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004604 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 17) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004605 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 18) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004606 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 19) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004607 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 20) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004608 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 21) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004609 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 22) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004610 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 23) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004611 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 24) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004612 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 25) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004613 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 26) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004614 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 52) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004640 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 53) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004641 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 54) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004642 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 55) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004643 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 1) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004644 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 2) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004645 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 3) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004646 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 4) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004647 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 5) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004648 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 6) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004649 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 7) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004650 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 8) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004651 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 9) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004652 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 10) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004653 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 11) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004654 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 12) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004655 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 13) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004656 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 14) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004657 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 15) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004658 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 16) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004659 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 17) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004660 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 18) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004661 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 19) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004662 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 20) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004663 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 21) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004664 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness lingual 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003491 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness medialorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003492 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness middletemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003493 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness parahippocampal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003494 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness paracentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003495 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness parsopercularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003496 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness parsorbitalis 21,281 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003497 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness parstriangularis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003498 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness pericalcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003499 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003500 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness posteriorcingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003501 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003502 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003503 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003504 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003505 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003506 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003507 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003508 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003509 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness frontalpole 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003510 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness transversetemporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003511 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003512 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003513 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003514 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA3a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003515 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness posteriorcingulate 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003467 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness precentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003468 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness precuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003469 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness rostralanteriorcingulate 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003470 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness rostralmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003471 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness superiorfrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003472 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness superiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003473 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness superiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003474 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness supramarginal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003475 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness frontalpole 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003476 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness transversetemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003477 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan lh thickness insula 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003478 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness GlobalMeanThickness 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003479 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness bankssts 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003480 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness caudalanteriorcingulate 21,282 British ancestry individuals 10,684 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003481 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness caudalmiddlefrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003482 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness cuneus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003483 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness entorhinal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003484 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness fusiform 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003485 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness inferiorparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003486 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness inferiortemporal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003487 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness isthmuscingulate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003488 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness lateraloccipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003489 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-Desikan rh thickness lateralorbitofrontal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003490 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA3b 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003516 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA4a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003517 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA4p 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003518 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA6 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003519 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA44 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003520 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness BA45 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003521 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness V1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003522 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness V2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003523 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness MT 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003524 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness perirhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003525 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo lh thickness entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003526 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003527 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003528 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA3a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003529 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA3b 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003530 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA4a 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003531 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA4p 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003532 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA6 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003533 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA44 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003534 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness BA45 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003535 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness V1 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003536 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness V2 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003537 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness MT 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003538 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness perirhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003539 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. BA-exvivo rh thickness entorhinal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003540 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 22) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004665 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 23) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004666 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 24) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004667 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 25) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004668 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 26) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004669 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 27) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004670 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 28) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004671 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 29) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004672 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 30) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004673 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 31) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004674 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 32) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004675 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 33) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004676 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 34) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004677 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 35) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004678 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 36) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004679 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 37) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004680 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 38) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004681 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 39) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004682 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 40) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004683 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 41) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004684 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 42) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004685 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 43) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004686 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 44) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004687 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 45) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004688 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 46) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004689 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI amplitudes (ICA100 node 27) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90004615 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-orbital-med-olfact 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003739 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-orbital-H-Shaped 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003740 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-parieto-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003741 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-pericallosal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003742 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-postcentral 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003743 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-precentral-inf-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003744 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-precentral-sup-part 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003745 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-suborbital 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003746 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-subparietal 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003747 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-temporal-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003748 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-temporal-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003749 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s rh thickness S-temporal-transverse 21,280 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003750 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity 3rd-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003751 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity 4th-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003752 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 40) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004893 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 41) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004894 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 42) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004895 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 43) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004896 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 44) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004897 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 45) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004898 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 46) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004899 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 47) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004900 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 48) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004901 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 49) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004902 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 50) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004903 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 51) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004904 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 52) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004905 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 53) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004906 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 54) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004907 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 55) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004908 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 56) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004909 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 57) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004910 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 58) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004911 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 59) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004912 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 60) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004913 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 61) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004914 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 62) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004915 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 63) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004916 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 64) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004917 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 65) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004918 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 66) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004919 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 67) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004920 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 68) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004921 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 69) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004922 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 70) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004923 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 71) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004924 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 72) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004925 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 73) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004926 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 74) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004927 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 75) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004928 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 76) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004929 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 77) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004930 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 78) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004931 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 79) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004932 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 80) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004933 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 81) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004934 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 82) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004935 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 83) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004936 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 84) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004937 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 85) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004938 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 86) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004939 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 87) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004940 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 88) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004941 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 89) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004942 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 90) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004943 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 91) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004944 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 92) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004945 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 93) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004946 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 94) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004947 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 95) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004948 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 96) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004949 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 97) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004950 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 98) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004951 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 99) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004952 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 100) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004953 Genome-wide genotyping array 2020-10-15 30157304 Vergara C 2018-09-11 Hum Mutat www.ncbi.nlm.nih.gov/pubmed/30157304 Association analysis of exome variants and refraction, axial length, and corneal curvature in a European-American population. Axial length 874 European ancestry individuals NA Illumina [1024985] (imputed) 0 axial length measurement http://www.ebi.ac.uk/efo/EFO_0005318 GCST010684 Exome genotyping array [Exome array] 2020-10-15 30157304 Vergara C 2018-09-11 Hum Mutat www.ncbi.nlm.nih.gov/pubmed/30157304 Association analysis of exome variants and refraction, axial length, and corneal curvature in a European-American population. Corneal curvature 883 European ancestry individuals NA Illumina [1024985] (imputed) 0 corneal topography http://www.ebi.ac.uk/efo/EFO_0004345 GCST010685 Exome genotyping array [Exome array] 2020-10-15 30157304 Vergara C 2018-09-11 Hum Mutat www.ncbi.nlm.nih.gov/pubmed/30157304 Association analysis of exome variants and refraction, axial length, and corneal curvature in a European-American population. Spherical equivalent 1,552 European ancestry individuals NA Illumina [1024985] (imputed) 0 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST010686 Exome genotyping array [Exome array] 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 222) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005075 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 223) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005076 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 224) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005077 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 225) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005078 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 226) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005079 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 227) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005080 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 228) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005081 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 229) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005082 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 230) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005083 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 231) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005084 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 232) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005085 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 233) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005086 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 234) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005087 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 235) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005088 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 236) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005089 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 237) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005090 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R planum temporale 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002542 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L supracalc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002543 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R supracalc cortex 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002544 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L occ pole 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002545 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R occ pole 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002546 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L thalamus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002547 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R thalamus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002548 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L caudate 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002549 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R caudate 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002550 Genome-wide genotyping array 2021-06-01 33168928 Wenric S 2020-11-10 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33168928 Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry. Rapid response to perioperative phenylephrine (change in mean arterial pressure) 1,082 African American individuals, 1,112 European ancestry individuals, 1,505 Hispanic individuals NA Illumina [42246687] (imputed) 2 blood pressure change measurement, response to phenylephrine http://www.ebi.ac.uk/efo/EFO_0006943, http://www.ebi.ac.uk/efo/EFO_0010152 GCST011771 Genome-wide genotyping array 2021-06-01 33168928 Wenric S 2020-11-10 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33168928 Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry. Rapid response to perioperative phenylephrine (change in diastolic blood pressure) 1,082 African American individuals, 1,112 European ancestry individuals, 1,505 Hispanic individuals NA Illumina [42246687] (imputed) 2 response to phenylephrine, diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0010152, http://www.ebi.ac.uk/efo/EFO_0006945 GCST011770 Genome-wide genotyping array 2021-06-01 33168928 Wenric S 2020-11-10 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33168928 Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry. Rapid response to perioperative phenylephrine (change in systolic blood pressure) 1,082 African American individuals, 1,112 European ancestry individuals, 1,505 Hispanic individuals NA Illumina [42246687] (imputed) 4 response to phenylephrine, systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0010152, http://www.ebi.ac.uk/efo/EFO_0006944 GCST011772 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- monocyte %monocyte 3,042 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18132558] (imputed) 6 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001451 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c+ CD62L- monocyte Absolute Count 3,017 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18121744] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001452 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c+ CD62L- monocyte %monocyte 3,040 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18132322] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001453 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- HLA DR++ monocyte Absolute Count 3,018 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18121877] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001454 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- HLA DR++ monocyte %monocyte 3,041 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18132452] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001455 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c+ HLA DR++ monocyte Absolute Count 3,019 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18122507] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001456 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD11c+ HLA DR++ monocyte %monocyte 3,042 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18133084] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001457 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Myeloid Dendritic Cell Absolute Count 3,387 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18342043] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001458 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Myeloid Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001459 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Plasmacytoid Dendritic Cell Absolute Count 3,374 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332528] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001460 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Dendritic Cell Absolute Count 3,374 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332528] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001461 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- Dendritic Cell Absolute Count 3,387 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18342043] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001462 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001463 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86+ myeloid Dendritic Cell Absolute Count 3,387 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18342043] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001464 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86+ myeloid Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001465 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86+ plasmacytoid Dendritic Cell Absolute Count 3,374 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332528] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001466 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD86+ plasmacytoid Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001467 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- myeloid Dendritic Cell Absolute Count 3,387 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18342043] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001468 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- myeloid Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001469 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- plasmacytoid Dendritic Cell Absolute Count 3,374 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18332528] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001470 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- plasmacytoid Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001471 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- CD86+ myeloid Dendritic Cell Absolute Count 3,387 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18342043] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001472 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L- CD86+ myeloid Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001473 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Plasmacytoid Dendritic Cell %Dendritic Cell 3,410 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18351549] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001474 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR++ monocyte %monocyte 3,595 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380843] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001475 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR++ monocyte %leukocyte 3,595 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380843] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001476 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR++ monocyte Absolute Count 3,579 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18377365] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001477 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. T/B cell 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001588 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+/CD8+ T cell 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001589 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+ T cell Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001590 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+ T cell %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001591 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8+ T cell Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001592 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8+ T cell %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001593 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+CD8+ T cell Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001594 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+CD8+ T cell %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001595 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8dim T cell Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001596 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8dim T cell %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001597 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4-CD8- T cell Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001598 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4-CD8- T cell %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001599 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Leukocyte Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001600 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Lymphocyte Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001601 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Lymphocyte %leukocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001602 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. T cell Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001603 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. T cell %lymphocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001604 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. T cell %leukocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001605 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+ T cell %leukocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001606 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8+ T cell %leukocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001607 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+CD8+ T cell %leukocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001608 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+ CD8dim T cell Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001609 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+ CD8dim T cell %lymphocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001610 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1203) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006056 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1204) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006057 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1205) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006058 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1206) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006059 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1207) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006060 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1208) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006061 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1209) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006062 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1210) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006063 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1211) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006064 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1212) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006065 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1213) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006066 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1214) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006067 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1215) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006068 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 608) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005461 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1216) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006069 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1217) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006070 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1218) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006071 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1219) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006072 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1220) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006073 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1221) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006074 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1222) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006075 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1223) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006076 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1224) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006077 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1225) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006078 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1226) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006079 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1128) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005981 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1129) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005982 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1130) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005983 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1131) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005984 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1132) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005985 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1133) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005986 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1134) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005987 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1135) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005988 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1136) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005989 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1137) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005990 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1138) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005991 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1139) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005992 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1140) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005993 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1141) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005994 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1142) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005995 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1143) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005996 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1144) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005997 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1145) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005998 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1146) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90005999 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1147) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006000 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1148) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006001 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1149) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006002 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1150) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006003 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1151) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006004 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1152) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006005 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1178) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006031 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1179) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006032 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1180) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006033 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1181) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006034 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1182) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006035 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1183) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006036 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1184) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006037 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1185) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006038 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1186) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006039 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1187) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006040 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1188) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006041 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1189) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006042 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1190) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006043 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1191) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006044 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1192) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006045 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1193) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006046 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1194) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006047 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1195) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006048 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1196) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006049 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1197) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006050 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1198) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006051 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1199) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006052 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1200) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006053 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1201) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006054 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1202) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006055 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1227) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006080 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1228) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006081 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1229) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006082 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1230) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006083 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1231) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006084 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1232) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006085 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1233) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006086 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1234) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006087 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1235) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006088 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1236) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006089 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1237) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006090 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1238) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006091 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1239) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006092 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1240) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006093 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1241) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006094 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1242) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006095 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1243) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006096 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1244) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006097 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1245) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006098 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1246) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006099 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1247) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006100 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1248) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006101 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1249) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006102 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1250) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006103 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1251) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006104 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1252) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006105 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1253) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006106 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1254) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006107 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1255) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006108 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1256) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006109 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1257) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006110 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1258) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006111 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1259) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006112 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1260) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006113 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1261) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006114 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1262) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006115 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1263) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006116 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1264) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006117 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1265) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006118 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1266) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006119 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1267) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006120 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1268) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006121 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1269) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006122 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1270) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006123 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1271) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006124 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1272) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006125 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1273) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006126 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1274) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006127 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1275) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006128 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1276) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006129 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1153) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006006 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1154) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006007 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1155) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006008 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1156) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006009 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1157) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006010 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1158) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006011 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1159) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006012 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1160) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006013 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1161) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006014 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1162) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006015 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1163) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006016 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1164) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006017 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1165) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006018 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1166) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006019 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1167) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006020 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1168) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006021 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1169) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006022 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1170) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006023 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1171) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006024 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1172) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006025 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1173) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006026 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1174) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006027 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1175) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006028 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1176) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006029 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1177) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006030 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on transitional B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001819 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on IgD+ CD24+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238197] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001820 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on IgD+ CD24- B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238174] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001821 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on IgD+ CD38- B cell 3,642 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18233905] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001822 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on IgD+ CD38- unswitched memory B cell 1,834 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17042369] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001823 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on IgD+ CD38+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238289] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001824 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on IgD+ CD38dim B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238174] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001825 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on unswitched memory B cell 3,636 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18230756] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001826 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on IgD+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238203] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001827 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD on transitional B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001828 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on B cell 3,660 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238700] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001829 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on CD20- B cell 3,648 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18233862] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001830 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L on CD62L+ myeloid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926605] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001831 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L on CD62L+ plasmacytoid Dendritic Cell 2,872 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926607] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001832 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L on CD62L+ Dendritic Cell 2,871 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17926566] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001833 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L on monocyte 2,848 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914264] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001834 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD62L on granulocyte 2,849 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17914380] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001835 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD66b on CD66b++ myeloid cell 1,465 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16829575] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001836 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD66b on Granulocytic Myeloid-Derived Suppressor Cells 1,244 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [16551140] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001837 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on naive CD8+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 8 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001838 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Effector Memory CD8+ T cell 2,912 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945888] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001839 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Terminally Differentiated CD8+ T cell 2,911 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945853] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001840 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Central Memory CD4+ T cell 2,912 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945888] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001841 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Naive CD4+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945511] (imputed) 8 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001842 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Effector Memory CD4+ T cell 2,912 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945888] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001843 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on CD20- CD38- B cell 3,606 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18223593] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001744 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on CD24+ CD27+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001745 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ CD24+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001746 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ CD24- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001747 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ CD38- B cell 3,645 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18234152] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001748 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ CD38- naive B cell 1,834 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17042256] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001749 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ CD38- unswitched memory B cell 1,836 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17043078] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001750 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ CD38+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001751 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 7 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001752 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD- CD24- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001753 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD- CD27- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001754 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD- CD38- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001755 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD- CD38+ B cell 3,659 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238670] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001756 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD- CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001757 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001758 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on naive-mature B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001759 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on unswitched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001760 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on switched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001761 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on IgD+ B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238340] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001762 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on transitional B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001763 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on CD24+ CD27+ B cell 3,654 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237589] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001764 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on IgD+ CD24+ B cell 3,655 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237790] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001765 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on IgD+ CD38- B cell 3,638 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18229172] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001766 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on IgD+ CD38- unswitched memory B cell 1,832 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17033107] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001767 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on IgD+ CD38+ B cell 3,655 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237787] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001768 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD127- CD25++ CD8+ T cell %T cell 3,162 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18208347] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001673 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD127- CD25++ CD8+ T cell %CD8+ T cell 3,162 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18208347] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001674 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD127- CD25++ CD8+ T cell Absolute Count 3,130 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18189521] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001675 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD25++ CD8+ T cell %T cell 3,162 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18208347] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001676 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD25++ CD8+ T cell %CD8+ T cell 3,162 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18208347] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001677 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD25++ CD8+ T cell Absolute Count 3,130 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18189521] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001678 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD8+ T cell %T cell 3,162 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18208347] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001679 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD8+ T cell %CD8+ T cell 3,162 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18208347] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001680 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25++ CD8+ T cell Absolute Count 3,130 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18189521] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001681 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127- CD8+ T cell %T cell 3,403 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18339725] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001682 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127- CD8+ T cell %CD8+ T cell 3,403 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18339725] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001683 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD127- CD8+ T cell Absolute Count 3,371 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18321960] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001684 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD8+ T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001685 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD8+ T cell %CD8+ T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001686 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD8+ T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001687 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA+ CD8+ T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001688 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA+ CD8+ T cell %CD8+ T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001689 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA+ CD8+ T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001690 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA- CD8+ T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001691 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA- CD8+ T cell %CD8+ T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001692 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28+ CD45RA- CD8+ T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340221] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001693 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD28- CD4-CD8- T cell %T cell 3,440 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18357815] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001694 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA- CD28- CD8+ T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340681] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001695 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA- CD28- CD8+ T cell %CD8+ T cell 3,425 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18344370] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001696 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA- CD28- CD8+ T cell %T cell 3,425 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18344370] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001697 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238340] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001794 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on transitional B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001795 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on CD20- B cell 3,634 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224904] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001796 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on CD20- CD38- B cell 3,592 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18211856] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001797 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on CD24+ CD27+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001798 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on T cell 1,838 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17043468] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001799 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on IgD+ CD24+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238284] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001800 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on IgD+ CD38- unswitched memory B cell 1,836 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17043294] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001801 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on IgD- CD38- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001802 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on IgD- CD38+ B cell 3,642 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18233708] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001803 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on IgD- CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001804 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001805 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on unswitched memory B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238284] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001806 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on Plasma Blast-Plasma Cell 3,651 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18236544] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001807 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD27 on switched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001808 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on CD20- B cell 3,630 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18230217] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001809 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on CD3- CD19- 1,834 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17037779] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001810 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on IgD+ CD24- B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238281] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001811 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on IgD+ CD38+ B cell 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238137] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001812 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on IgD+ CD38dim B cell 3,654 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238118] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001813 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on IgD- CD38+ B cell 3,644 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18236636] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001814 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on IgD- CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001815 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on naive-mature B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238281] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001816 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on Plasma Blast-Plasma Cell 3,655 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238244] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001817 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD38 on IgD+ B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238556] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001818 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA+ CD28- CD8+ T cell Absolute Count 3,408 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18340681] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001698 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA+ CD28- CD8+ T cell %CD8+ T cell 3,425 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18344370] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001699 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD45RA+ CD28- CD8+ T cell %T cell 3,425 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18344370] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001700 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14- CD16+ monocyte Absolute Count 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001579 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14+ CD16+ monocyte Absolute Count 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001580 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14- CD16- Absolute Count 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 4 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001581 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14+ CD16- monocyte Absolute Count 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 3 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001582 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Monocyte Absolute Count 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001583 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14- CD16+ monocyte %monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 2 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001584 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14+ CD16+ monocyte %monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 2 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001585 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD14+ CD16- monocyte %monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001586 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD16+ monocyte %monocyte 3,629 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18224179] (imputed) 1 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90001587 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Hematopoietic Stem Cell Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001514 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Immature Myeloid-Derived Suppressor Cells Absolute Count 1,857 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203507] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001515 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Immature Myeloid-Derived Suppressor Cells %CD33dim HLA DR- CD66b- 1,857 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203507] (imputed) 2 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001516 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33+ HLA DR+ Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001517 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33+ HLA DR+ CD14- Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001518 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33+ HLA DR+ CD14- %CD33+ HLA DR+ 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001519 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33+ HLA DR+ CD14dim Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 2 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001520 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33+ HLA DR+ CD14dim %CD33+ HLA DR+ 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001521 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33- HLA DR- Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001522 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33- HLA DR+ Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 2 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001523 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Granulocytic Myeloid-Derived Suppressor Cells Absolute Count 1,856 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17202429] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001524 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33dim HLA DR+ CD11b+ Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001525 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33dim HLA DR+ CD11b+ %CD33dim HLA DR+ 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 2 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001526 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33dim HLA DR+ CD11b- Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 3 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001527 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33dim HLA DR+ CD11b- %CD33dim HLA DR+ 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 2 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001528 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD66b++ myeloid cell Absolute Count 1,858 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203588] (imputed) 0 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001529 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Monocytic Myeloid-Derived Suppressor Cells Absolute Count 1,855 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17197940] (imputed) 2 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001530 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD33dim HLA DR- Absolute Count 1,856 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203446] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001531 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Basophil Absolute Count 1,857 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203507] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001532 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Basophil %CD33dim HLA DR- CD66b- 1,857 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17203507] (imputed) 1 myeloid white cell count http://www.ebi.ac.uk/efo/EFO_0007988 GCST90001533 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on CD20- CD38- B cell 3,592 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18217315] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001701 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on CD24+ CD27+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001702 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ CD24+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001703 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ CD24- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001704 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ CD38- B cell 3,645 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18234152] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001705 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ CD38- naive B cell 1,837 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17043358] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001706 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ CD38- unswitched memory B cell 1,837 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17043358] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001707 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ CD38+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238081] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001708 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001709 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD- CD24- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001710 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD- CD27- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001711 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD- CD38- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001712 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD- CD38+ B cell 3,659 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238670] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001713 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD- CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001714 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001715 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on naive-mature B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001716 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on unswitched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001717 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on switched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001718 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on IgD- CD38- B cell 3,648 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18233041] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001769 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on IgD- CD38dim B cell 3,649 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18231767] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001770 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on memory B cell 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237721] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001771 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on unswitched memory B cell 3,655 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237790] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001772 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on switched memory B cell 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237700] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001773 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24 on transitional B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238267] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001774 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on B cell 3,660 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238700] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001775 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD20- CD38- B cell 3,505 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18188611] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001776 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on CD24+ CD27+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001777 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ CD24+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001778 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ CD24- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001779 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ CD38- B cell 3,642 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18233845] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001780 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ CD38- naive B cell 1,835 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17043071] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001781 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ CD38- unswitched memory B cell 1,837 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17043358] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001782 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ CD38+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238289] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001783 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD+ CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001784 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD- CD24- B cell 3,649 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18236139] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001785 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD- CD27- B cell 3,651 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18236953] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001786 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD- CD38- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001787 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD- CD38+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238567] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001788 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on IgD- CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001789 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001790 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on naive-mature B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001791 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on unswitched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001792 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD25 on switched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001793 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Terminally Differentiated CD4+ T cell 2,903 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17944758] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001844 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD45RA- CD4+ T cell 2,911 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945546] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001845 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Central Memory CD8+ T cell 2,910 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17945467] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001846 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on HLA DR+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001847 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on Natural Killer T 3,113 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18030777] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001848 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on HLA DR+ CD4+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001849 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on HLA DR+ CD8+ T cell 3,060 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18012714] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001850 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001851 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD39+ resting CD4 regulatory T cell 2,649 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17852537] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001852 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on activated CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001853 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD39+ activated CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001854 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on secreting CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001855 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD39+ secreting CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001856 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on activated & secreting CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 5 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001857 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD45RA+ CD4+ T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 9 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001858 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD8+ T cell 2,918 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17947121] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001859 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD39+ CD4+ T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001860 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD28+ CD4+ T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001861 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD28+ CD4-CD8- T cell 2,918 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954394] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001862 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD28+ CD45RA- CD8+ T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001863 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD28+ CD45RA+ CD8+ T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001864 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD28- CD8+ T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001865 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD39+ CD8+ T cell 2,914 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17951421] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001866 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD4+ T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001867 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3 on CD4 regulatory T cell 2,919 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17954450] (imputed) 6 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001868 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on IgD+ B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238340] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001719 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. BAFF-R on transitional B cell 3,655 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237486] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001720 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on CD20- B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238022] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001721 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on CD20- CD38- B cell 3,595 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18220019] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001722 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on CD24+ CD27+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238264] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001723 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ CD24+ B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238264] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001724 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ CD24- B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18234782] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001725 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ CD38- B cell 3,645 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18234152] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001726 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ CD38- naive B cell 1,830 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17034416] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001727 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ CD38- unswitched memory B cell 1,833 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [17042652] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001728 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ CD38+ B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001729 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001730 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD- CD24- B cell 3,655 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18234272] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001731 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD- CD27- B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18237800] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001732 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD- CD38- B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001733 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD- CD38+ B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238609] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001734 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD- CD38dim B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001735 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001736 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on naive-mature B cell 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18234616] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001737 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on unswitched memory B cell 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238264] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001738 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on Plasma Blast-Plasma Cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238621] (imputed) 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001739 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on switched memory B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001740 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on IgD+ B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238340] (imputed) 1 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001741 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD19 on transitional B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001742 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20 on B cell 3,660 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238700] (imputed) 4 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90001743 Genome-wide genotyping array 2021-05-07 33134509 Tang ME 2020-09-10 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/33134509 Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia. Serum type 1 collagen metabolite levels 4,891 Danish ancestry individuals NA Illumina [7672338] (imputed) 4 matrix metalloproteinase–degraded type I collagen measurement http://www.ebi.ac.uk/efo/EFO_0011036 GCST011622 Genome-wide genotyping array 2021-05-07 33134509 Tang ME 2020-09-10 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/33134509 Matrix metalloproteinase-degraded type I collagen is associated with APOE/TOMM40 variants and preclinical dementia. Serum total cholesterol levels 4,891 Danish ancestry individuals NA NR [NR] 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST011621 Genome-wide genotyping array 2021-03-30 33723403 Sha Z 2021-03-15 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33723403 The genetic architecture of structural left-right asymmetry of the human brain. Left–right brain asymmetry 32,256 European ancestry individuals NA NR [9312144] (imputed) 27 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90010427 Genome-wide genotyping array 2022-01-19 34964454 Gentiluomo M 2021-11-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34964454 Genome-wide association study of mitochondrial copy number. Mitochondrial DNA copy number 6,836 European ancestry individuals NA Illumina [6374524] (imputed) 9 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90019040 Genome-wide genotyping array 2022-01-19 34964454 Gentiluomo M 2021-11-23 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34964454 Genome-wide association study of mitochondrial copy number. Mitochondrial DNA copy number 6,836 European ancestry individuals, 295,150 individuals NA Illumina [2775252] (imputed) 2 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST012656 Genome-wide genotyping array 2021-02-05 33137956 Yang Y 2020-10-29 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/33137956 Secondary Genome-Wide Association Study Using Novel Analytical Strategies Disentangle Genetic Components of Cleft Lip and/or Cleft Palate in 1q32.2. Orofacial clefts 160 African ancestry cases, 584 Asian ancestry cases, 1,068 European ancestry cases, 37 Native American ancestry cases, 849 admixed ancestry cases, 5 cases, 219 African ancestry controls, 1,433 Asian ancestry controls, 3,563 European ancestry controls, 152 Native American ancestry controls, 2,420 admixed ancestry controls, 52 controls NA Illumina [at least 589945] (imputed) 10 Orofacial cleft http://purl.obolibrary.org/obo/HP_0000202 GCST011088 Genome-wide genotyping array 2022-01-14 33418499 Lin BM 2021-01-06 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/33418499 Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium. Estimated glomerular filtration rate 8,459 African American individuals, 1,182 Hispanic/Latino individuals, 2,208 East Asian ancestry individuals, 11,837 European ancestry individuals, 46 Native American ancestry individuals 2,637 East Asian ancestry individuals, 6,767 Hispanic/Latino individuals, 3,031 Native American ancestry individuals NR [43622178] 13 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90093093 Genome-wide sequencing 2021-06-01 33179336 Syreeni A 2020-11-11 J Intern Med www.ncbi.nlm.nih.gov/pubmed/33179336 Genome-wide search for genes affecting the age at diagnosis of type 1 diabetes. Type 1 diabetes (age at diagnosis) 12,539 European ancestry individuals NA Affymetrix, Illumina [7374092] (imputed) 39 age at diagnosis, type 1 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0005147 GCST011773 Genome-wide genotyping array 2022-01-20 33600772 Somineni HK 2021-02-17 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33600772 Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Inflammatory bowel disease 1,774 African American cases, 1,644 African American controls NA NR [93400000] 1 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90093115 Genome-wide sequencing 2022-01-20 33600772 Somineni HK 2021-02-17 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33600772 Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Crohn's disease 1,335 African American cases, 1,644 African American controls NA NR [93400000] 1 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90093116 Genome-wide sequencing 2022-01-20 33600772 Somineni HK 2021-02-17 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33600772 Whole-genome sequencing of African Americans implicates differential genetic architecture in inflammatory bowel disease. Ulcerative colitis 407 African American cases, 1,644 African American controls NA NR [93400000] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90093117 Genome-wide sequencing 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Eye morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 3 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST012063 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Upper cheek morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST012062 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Chin morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 1 chin morphology measurement http://www.ebi.ac.uk/efo/EFO_0007842 GCST012061 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Nose morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 5 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST012060 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Cheekbone morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST012059 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Lower cheek morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST012058 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Forehead morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 0 forehead morphology measurement http://www.ebi.ac.uk/efo/EFO_0007844 GCST012057 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Jaw morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST012056 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Mouth morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 1 mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007955 GCST012055 Genome-wide genotyping array 2021-07-27 33593615 Huang Y 2020-11-09 J Genet Genomics www.ncbi.nlm.nih.gov/pubmed/33593615 A genome-wide association study of facial morphology identifies novel genetic loci in Han Chinese. Profile morphology 2,659 Han Chinese ancestry individuals NA Illumina [4757938] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST012054 Genome-wide genotyping array 2021-01-14 30189721 Park B 2018-09-05 Cancer Res Treat www.ncbi.nlm.nih.gov/pubmed/30189721 Genome-Wide Association of Genetic Variation in the PSCA Gene with Gastric Cancer Susceptibility in a Korean Population. Gastric cancer 297 East Asian ancestry male cases, 153 East Asian ancestry female cases, 539 East Asian ancestry male controls, 595 East Asian ancestry female controls 533 East Asian ancestry male cases, 270 East Asian ancestry female cases, 1,648 East Asian ancestry male controls, 2,045 East Asian ancestry female controls Affymetrix [713348] (imputed) 1 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST010956 Exome genotyping array [Exome array] 2020-10-15 32953199 Liu Z 2019-03-01 J BioX Res www.ncbi.nlm.nih.gov/pubmed/32953199 Integrative omics analysis identifies macrophage migration inhibitory factor signaling pathways underlying human hepatic fibrogenesis and fibrosis. Liver fibrogenesis (alpha smooth muscle actin levels) 102 European ancestry individuals, 19 African ancestry individuals NA Illumina [533687] 8 liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0010576 GCST010677 Genome-wide genotyping array 2020-10-15 32953199 Liu Z 2019-03-01 J BioX Res www.ncbi.nlm.nih.gov/pubmed/32953199 Integrative omics analysis identifies macrophage migration inhibitory factor signaling pathways underlying human hepatic fibrogenesis and fibrosis. Liver fibrosis (total hepatic collagen content) 102 European ancestry individuals, 19 African ancestry individuals NA Illumina [533687] 6 liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0010576 GCST010678 Genome-wide genotyping array 2022-01-20 34871226 Kim SY 2021-11-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/34871226 Genome-wide association study identifies BTNL2 associated with atopic asthma in children. Atopic asthma 243 East Asian ancestry child cases, 134 East Asian ancestry child controls NA Affymetrix [423461] 1 atopic asthma http://www.ebi.ac.uk/efo/EFO_0010638 GCST90093123 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or body fat percentage (pleiotropy) 100,716 individuals with body fat percentage measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] 1 Alzheimer disease, body fat percentage http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0007800 GCST90013832 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or BMI (pleiotropy) 681,275 individuals with BMI measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] 0 Alzheimer disease, body mass index http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90013833 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or coronary heart disease (pleiotropy) 34,541 coronary heart disease cases, 71,880 Alzheimer's disease cases, 645,362 controls NA NR [NR] 0 Alzheimer disease, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90013834 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or diastolic blood pressure (pleiotropy) 1,006,863 individuals with diastolic blood pressure measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] 3 Alzheimer disease, diastolic blood pressure http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0006336 GCST90013835 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or HDL levels (pleiotropy) 404,128 European ancestry individuals with HDL-C measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] (imputed) 1 Alzheimer disease, high density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90013836 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or LDL levels (pleiotropy) 404,128 European ancestry individuals with LDL-C measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] (imputed) 1 Alzheimer disease, low density lipoprotein cholesterol measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90013837 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or systolic blood pressure (pleiotropy) 1,006,863 individuals with systolic blood pressure measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] 1 Alzheimer disease, systolic blood pressure http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0006335 GCST90013838 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or total cholesterol levels (pleiotropy) 404,128 European ancestry individuals with total cholesterol measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] (imputed) 0 Alzheimer disease, total cholesterol measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004574 GCST90013839 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or triglycerides levels (pleiotropy) 404,128 European ancestry individuals with triglyceride measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] (imputed) 0 Alzheimer disease, triglyceride measurement http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004530 GCST90013840 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or type 2 diabetes (pleiotropy) 80,831 type 2 diabetes cases, 71,880 Alzheimer's disease cases, 1,200,677 controls NA NR [NR] 0 Alzheimer disease, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90013841 Genome-wide genotyping array 2021-03-22 33541420 Bone WP 2021-02-04 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/33541420 Multi-trait association studies discover pleiotropic loci between Alzheimer's disease and cardiometabolic traits. Alzheimer's disease or waist-hip ratio (pleiotropy) 649,649 individuals with waist-hip ratio measurements, 71,880 Alzheimer's disease cases, 383,378 controls NA NR [NR] 1 Alzheimer disease, waist-hip ratio http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0004343 GCST90013842 Genome-wide genotyping array 2021-03-01 33549134 Adolphe C 2021-02-06 Genome Med www.ncbi.nlm.nih.gov/pubmed/33549134 Genetic and functional interaction network analysis reveals global enrichment of regulatory T cell genes influencing basal cell carcinoma susceptibility. Basal cell carcinoma 17,416 European ancestry cases, 375,455 European ancestry controls NA Affymetrix [7260263] (imputed) 71 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90013410 Genome-wide genotyping array 2021-08-19 33737391 Ambati A 2021-03-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/33737391 Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci. Kleine-Levin syndrome 136 Asian ancestry cases, 3,123 Asian ancestry controls, 299 European ancestry cases, 9,373 European ancestry controls, 16 Latino cases, 1,980 Latino controls, 41 Ashkenazi Jewish ancestry cases, 183 Ashkenazi Jewish ancestry controls, 181 non-Ashkenazi Jewish ancestry cases, 680 non-Ashkenazi Jewish ancestry controls 171 cases, 1,956 controls Affymetrix [104626] (imputed) 1 Kleine-Levin Syndrome http://www.ebi.ac.uk/efo/EFO_1001354 GCST012212 Genome-wide genotyping array 2021-08-10 33727749 Hishida A 2021-02-01 Nagoya J Med Sci www.ncbi.nlm.nih.gov/pubmed/33727749 Genome-wide association study of serum prostate-specific antigen levels based on 1000 Genomes imputed data in Japanese: the Japan Multi-Institutional Collaborative Cohort Study. Prostate-specific antigen levels 1,216 Japanese ancestry men 2,447 Japanese ancestry men Illumina [6288024] (imputed) 0 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST012175 Genome-wide genotyping array 2021-11-12 33606446 Kim SK 2021-02-18 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/33606446 Identification of Three Loci Associated with Achilles Tendon Injury Risk from a Genome-wide Association Study. Achilles tendon injury 12,354 European ancestry cases, 483,080 European ancestry controls NA Affymetrix [10183576] (imputed) 5 Achilles tendon injury http://www.ebi.ac.uk/efo/EFO_0600078 GCST012501 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. HDL levels x SSRI levels interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 1 response to selective serotonin reuptake inhibitor, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0004612 GCST012330 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. LDL levels x SSRI levels interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 1 low density lipoprotein cholesterol measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0005658 GCST012329 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. Total cholesterol levels x SSRI levels interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 1 total cholesterol measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0005658 GCST012328 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. Triglyceride levels x SSRI levels interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 0 triglyceride measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0005658 GCST012327 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. BMI x SSRI defined daily dose interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 4 response to selective serotonin reuptake inhibitor, body mass index http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0004340 GCST012326 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. HDL levels x SSRI defined daily dose interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 3 response to selective serotonin reuptake inhibitor, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0004612 GCST012325 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. LDL levels x SSRI defined daily dose interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 14 low density lipoprotein cholesterol measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0005658 GCST012324 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. Total cholesterol levels x SSRI defined daily dose interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 3 total cholesterol measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0005658 GCST012323 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. Triglyceride levels x SSRI defined daily dose interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 52 triglyceride measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0005658 GCST012322 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. BMI x SSRI levels (escitalopram or citalopram) interaction in schizophrenia or bipolar disorder 181 European ancestry individuals NA Illumina [NR] (imputed) 0 response to escitalopram, response to citalopram, body mass index http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329, http://www.ebi.ac.uk/efo/EFO_0004340 GCST012321 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. HDL levels x SSRI levels (escitalopram or citalopram) interaction in schizophrenia or bipolar disorder 181 European ancestry individuals NA Illumina [NR] (imputed) 2 response to escitalopram, response to citalopram, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329, http://www.ebi.ac.uk/efo/EFO_0004612 GCST012320 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. LDL levels x SSRI levels (escitalopram or citalopram) interaction in schizophrenia or bipolar disorder 181 European ancestry individuals NA Illumina [NR] (imputed) 18 low density lipoprotein cholesterol measurement, response to escitalopram, response to citalopram http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329 GCST012319 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. Total cholesterol levels x SSRI levels (escitalopram or citalopram) interaction in schizophrenia or bipolar disorder 181 European ancestry individuals NA Illumina [NR] (imputed) 5 total cholesterol measurement, response to escitalopram, response to citalopram http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329 GCST012318 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. Triglyceride levels x SSRI levels (escitalopram or citalopram) interaction in schizophrenia or bipolar disorder 181 European ancestry individuals NA Illumina [NR] (imputed) 16 triglyceride measurement, response to escitalopram, response to citalopram http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0007871, http://www.ebi.ac.uk/efo/EFO_0006329 GCST012317 Genome-wide genotyping array 2021-09-06 33824429 Fjukstad KK 2021-04-06 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/33824429 Genetic variants associated with cardiometabolic abnormalities during treatment with selective serotonin reuptake inhibitors: a genome-wide association study. BMI x SSRI levels interaction in schizophrenia or bipolar disorder 1,180 European ancestry individuals NA Illumina [NR] (imputed) 2 response to selective serotonin reuptake inhibitor, body mass index http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0004340 GCST012331 Genome-wide genotyping array 2021-09-03 33736632 Zeng Z 2021-03-18 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33736632 Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. Persistent hepatitis B virus infection 587 Chinese ancestry persistent cases, 275 Chinese ancestry clearance controls NA Affymetrix [607153] 4 susceptibility to hepatitis B infection measurement http://www.ebi.ac.uk/efo/EFO_0008405 GCST012289 Genome-wide genotyping array 2021-09-03 33736632 Zeng Z 2021-03-18 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33736632 Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. Chronic hepatitis B infection vs asymptomatic persistence 93 Chinese ancestry chronic hepatitis B cases, 92 Chinese ancestry asymptomatic persistence infection controls NA Affymetrix [607153] 1 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST012288 Genome-wide genotyping array 2021-09-03 33736632 Zeng Z 2021-03-18 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33736632 Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. Hepatitis B virus-related hepatocellular carcinoma vs chronic hepatitis B infection 214 Chinese ancestry hepatocellular carcinoma cases, 93 Chinese ancestry chronic hepatitis B controls NA Affymetrix [607153] 1 hepatitis virus-related hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0008505 GCST012287 Genome-wide genotyping array 2021-09-03 33736632 Zeng Z 2021-03-18 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33736632 Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. Hepatitis B virus-related hepatocellular carcinoma vs hepatitis B virus-related decompensated cirrhosis 214 Chinese ancestry hepatocellular carcinoma cases, 188 Chinese ancestry decompensated cirrhosis controls NA Affymetrix [607153] 1 hepatitis virus-related hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0008505 GCST012286 Genome-wide genotyping array 2021-09-03 33736632 Zeng Z 2021-03-18 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33736632 Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. Hepatitis B 460 Chinese ancestry cases, 169 Chinese ancestry controls NA Affymetrix [607153] 4 hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004197 GCST012285 Genome-wide genotyping array 2021-09-03 33736632 Zeng Z 2021-03-18 BMC Med Genomics www.ncbi.nlm.nih.gov/pubmed/33736632 Genome-wide association study identifies new loci associated with risk of HBV infection and disease progression. Development of chronic hepatitis B up to 495 Chinese ancestry cases, up to 367 Chinese ancestry controls NA Affymetrix [607153] 1 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST012284 Genome-wide genotyping array 2021-04-27 33514426 Tan LK 2021-01-30 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/33514426 The spectrum of association in HLA region with rheumatoid arthritis in a diverse Asian population: evidence from the MyEIRA case-control study. Rheumatoid arthritis 530 Malay ancestry cases, 259 Chinese ancestry cases, 412 Asian Indian ancestry cases, 59 cases, 981 Malay ancestry controls, 205 Chinese ancestry controls, 297 Asian Indian controls, 87 controls NA Illumina [113576] 1 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST011558 Targeted genotyping array [ImmunoChip] 2021-04-27 33514426 Tan LK 2021-01-30 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/33514426 The spectrum of association in HLA region with rheumatoid arthritis in a diverse Asian population: evidence from the MyEIRA case-control study. Rheumatoid arthritis (ACPA-positive) 530 Malay ancestry cases, 259 Chinese ancestry cases, 412 Asian Indian ancestry cases, 59 cases, 981 Malay ancestry controls, 205 Chinese ancestry controls, 297 Asian Indian controls, 87 controls NA Illumina [113576] 1 ACPA-positive rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0009459 GCST011557 Targeted genotyping array [ImmunoChip] 2021-04-27 33514426 Tan LK 2021-01-30 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/33514426 The spectrum of association in HLA region with rheumatoid arthritis in a diverse Asian population: evidence from the MyEIRA case-control study. Rheumatoid arthritis (ACPA-negative) 530 Malay ancestry cases, 259 Chinese ancestry cases, 412 Asian Indian ancestry cases, 59 cases, 981 Malay ancestry controls, 205 Chinese ancestry controls, 297 Asian Indian controls, 87 controls NA Illumina [113576] 1 ACPA-negative rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0009460 GCST011556 Targeted genotyping array [ImmunoChip] 2021-04-30 33842983 Chung RH 2021-04-12 Diabetologia www.ncbi.nlm.nih.gov/pubmed/33842983 Multi-omics analysis identifies CpGs near G6PC2 mediating the effects of genetic variants on fasting glucose. Fasting blood glucose 18,122 Han Chinese ancestry individuals 1,989 Han Chinese ancestry individuals Affymetrix [774398] (imputed) 18 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST011587 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (four or five) 4,887 European ancestry cases, 232,552 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014426 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (four or five) vs mental health questionnaire controls 4,887 European ancestry cases, 57,805 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014427 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Lifetime depression (mental health questionnaire) 28,982 European ancestry cases, 232,552 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014428 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Lifetime depression (mental health questionnaire) vs mental health questionnaire controls 28,982 European ancestry cases, 57,805 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014429 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (one) 57,321 European ancestry cases, 232,552 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014430 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (one) vs mental health questionnaire controls 57,321 European ancestry cases, 57,805 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014431 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (three) 9,738 European ancestry cases, 232,552 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014432 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (three) vs mental health questionnaire controls 9,738 European ancestry cases, 57,805 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014433 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (two) 21,468 European ancestry cases, 232,552 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014434 Genome-wide genotyping array 2021-04-19 33541459 Glanville KP 2021-02-05 BJPsych Open www.ncbi.nlm.nih.gov/pubmed/33541459 Multiple measures of depression to enhance validity of major depressive disorder in the UK Biobank. Endorsed measures of depression (two) vs mental health questionnaire controls 21,468 European ancestry cases, 57,805 European ancestry controls NA NR [9940918] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90014435 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 121) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004764 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 122) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004765 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 123) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004766 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 124) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004767 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 125) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004768 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 126) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004769 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 127) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004770 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 128) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004771 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 129) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004772 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 130) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004773 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 131) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004774 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 132) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004775 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 133) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004776 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 134) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004777 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 135) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004778 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 136) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004779 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 137) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004780 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness Lat-Fis-post 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003643 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness Pole-occipital 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003644 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness Pole-temporal 21,281 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003645 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-calcarine 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003646 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003647 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-cingul-Marginalis 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003648 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-circular-insula-ant 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003649 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-circular-insula-inf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003650 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aparc-a2009s lh thickness S-circular-insula-sup 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90003651 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 138) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004781 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 139) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004782 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 140) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004783 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 141) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004784 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 142) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004785 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 143) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004786 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 144) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004787 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 145) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004788 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 146) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004789 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 147) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004790 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 148) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004791 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 149) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004792 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 150) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004793 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 151) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004794 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 152) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004795 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 153) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004796 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 154) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004797 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 155) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004798 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 156) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004799 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 157) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004800 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 158) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004801 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 159) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004802 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 160) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004803 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 161) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004804 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 96) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004739 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 97) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004740 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 98) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004741 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 99) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004742 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 100) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004743 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 101) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004744 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 102) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004745 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 103) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004746 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 104) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004747 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 105) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004748 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 106) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004749 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 107) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004750 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 108) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004751 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 109) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004752 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 110) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004753 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 111) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004754 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 112) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004755 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 113) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004756 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 114) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004757 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 115) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004758 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 116) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004759 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 117) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004760 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 118) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004761 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 119) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004762 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 120) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004763 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 187) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004830 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 188) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004831 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 189) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004832 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 190) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004833 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 191) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004834 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 192) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004835 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 193) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004836 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 194) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004837 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 195) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004838 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 196) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004839 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 197) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004840 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 198) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004841 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 199) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004842 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 200) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004843 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 201) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004844 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 202) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004845 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 203) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004846 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 204) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004847 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 205) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004848 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 206) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004849 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 207) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004850 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 208) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004851 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 209) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004852 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 210) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004853 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004854 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 162) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004805 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 163) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004806 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 164) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004807 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 165) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004808 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 166) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004809 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 167) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004810 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 168) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004811 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 169) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004812 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 170) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004813 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 171) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004814 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 172) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004815 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 173) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004816 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 174) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004817 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 175) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004818 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 176) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004819 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 177) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004820 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 178) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004821 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 179) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004822 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 180) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004823 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 181) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004824 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 182) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004825 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 183) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004826 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 184) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004827 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 185) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004828 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA25 edge 186) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004829 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 2) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004855 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 3) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004856 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 4) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004857 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 5) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004858 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 6) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004859 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 7) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004860 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 8) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004861 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 9) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004862 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 10) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004863 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 11) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004864 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 12) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004865 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 13) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004866 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 14) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004867 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 15) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004868 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 16) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004869 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 17) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004870 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 18) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004871 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 19) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004872 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 20) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004873 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 21) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004874 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 22) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004875 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 23) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004876 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 24) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004877 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 25) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004878 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 26) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004879 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 101) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004954 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 102) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004955 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 103) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004956 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 104) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004957 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 105) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004958 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 106) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004959 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 107) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004960 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 108) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004961 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 109) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004962 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 110) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004963 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 111) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004964 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 112) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004965 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 113) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004966 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 114) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004967 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 115) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004968 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 116) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004969 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 117) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004970 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 118) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004971 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 119) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004972 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 120) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004973 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 121) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004974 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 122) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004975 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 123) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004976 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 124) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004977 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 125) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90004978 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity 5th-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003753 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity Brain-Stem 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003754 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity CSF 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003755 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity WM-hypointensities 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003756 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity non-WM-hypointensities 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003757 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity Optic-Chiasm 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003758 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity CC-Posterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003759 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity CC-Mid-Posterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003760 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity CC-Central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003761 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity CC-Mid-Anterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003762 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global intensity CC-Anterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003763 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Lateral-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003764 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Inf-Lat-Vent 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003765 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Cerebellum-White-Matter 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003766 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Cerebellum-Cortex 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003767 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Thalamus-Proper 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 2 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003768 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Caudate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003769 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Putamen 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 7 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003770 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Pallidum 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003771 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Hippocampus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003772 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Amygdala 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003773 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity Accumbens-area 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003774 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity VentralDC 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003775 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity vessel 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003776 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh intensity choroid-plexus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90003777 Genome-wide genotyping array 2021-03-22 33580673 Thorolfsdottir RB 2021-02-13 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/33580673 Genetic insight into sick sinus syndrome. Sick sinus syndrome 6,189 European ancestry cases, 931,046 European ancestry controls 280 Norwegian ancestry cases, 69,141 Norwegian ancestry controls Affymetrix, Illumina [NR] (imputed) 6 familial sick sinus syndrome http://purl.obolibrary.org/obo/MONDO_0012061 GCST011360 Genome-wide genotyping array 2021-03-31 33717105 Donkel SJ 2021-02-24 Front Immunol www.ncbi.nlm.nih.gov/pubmed/33717105 Common and Rare Variants Genetic Association Analysis of Circulating Neutrophil Extracellular Traps. Myeloperoxidase-DNA complexes 5,590 European ancestry individuals NA Illumina [11789982] (imputed) 9 myeloperoxidase (MPO)-DNA complex measurement http://www.ebi.ac.uk/efo/EFO_0011039 GCST90013658 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum VIIb 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002576 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum VIIb 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002577 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum VIIIa 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002578 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum VIIIa 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002579 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum VIIIa 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002580 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum VIIIb 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002581 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum VIIIb 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002582 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum VIIIb 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002583 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum IX 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002584 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum IX 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002585 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum IX 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002586 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum X 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002587 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum X 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002588 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum X 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002589 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume BrainSeg 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002590 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume BrainSegNotVent 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002591 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume BrainSegNotVentSurf 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002592 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume SubCortGray 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002593 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume TotalGray 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002594 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume SupraTentorial 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002595 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume SupraTentorialNotVent 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002596 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume EstimatedTotalIntraCranial 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002597 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume VentricleChoroid 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002598 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume 3rd-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002599 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume 4th-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002600 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L putamen 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002551 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R putamen 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002552 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L pallidum 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002553 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R pallidum 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002554 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L hippocampus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002555 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R hippocampus 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002556 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L amygdala 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002557 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R amygdala 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002558 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L ventral striatum 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002559 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R ventral striatum 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002560 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs brain stem 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002561 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum I-IV 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002562 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum I-IV 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002563 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum V 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002564 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum V 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002565 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum VI 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002566 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum VI 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002567 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum VI 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002568 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum crus I 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002569 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum crus I 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002570 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum crus I 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 7 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002571 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum crus II 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002572 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs V cerebellum crus II 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002573 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs R cerebellum crus II 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 6 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002574 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. IDP T1 FAST ROIs L cerebellum VIIb 22,133 British ancestry individuals 11,086 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002575 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume 5th-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002601 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume Brain-Stem 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002602 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume CSF 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002603 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume WM-hypointensities 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002604 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume non-WM-hypointensities 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002605 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume Optic-Chiasm 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002606 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume CC-Posterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002607 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume CC-Mid-Posterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002608 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume CC-Central 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002609 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume CC-Mid-Anterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002610 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume CC-Anterior 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002611 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume-ratio BrainSegVol-to-eTIV 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002612 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg global volume-ratio MaskVol-to-eTIV 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002613 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Cortex 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002614 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume CerebralWhiteMatter 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002615 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Lateral-Ventricle 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002616 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Inf-Lat-Vent 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 2 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002617 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Cerebellum-White-Matter 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002618 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Cerebellum-Cortex 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 5 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002619 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Thalamus-Proper 21,282 British ancestry individuals 10,685 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002620 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Caudate 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002621 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Putamen 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 3 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002622 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Pallidum 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 1 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002623 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Hippocampus 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 4 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002624 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. aseg lh volume Amygdala 21,282 British ancestry individuals 10,686 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006930 GCST90002625 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4+ CD8dim T cell %leukocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001611 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8dim T cell %leukocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001612 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4-CD8- T cell %leukocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001613 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8+ and CD8dim T cell %leukocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001614 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. TCRgd T cell Absolute Count 3,650 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427099] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001615 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. TCRgd T cell %T cell 3,666 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430537] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001616 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. TCRgd T cell %lymphocyte 3,666 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430537] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001617 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ T cell Absolute Count 3,580 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18377392] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001618 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ T cell%T cell 3,596 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380873] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001619 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ T cell%lymphocyte 3,596 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380873] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001620 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Natural Killer T Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001621 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Natural Killer T %T cell 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001622 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Natural Killer T %lymphocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001623 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ CD4+ T cell Absolute Count 3,579 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18377359] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001624 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ CD4+ T cell %T cell 3,595 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380839] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001625 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ CD4+ T cell %lymphocyte 3,595 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380839] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001626 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ CD8+ T cell Absolute Count 3,579 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18377359] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001627 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ CD8+ T cell %T cell 3,595 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380839] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001628 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ CD8+ T cell %lymphocyte 3,595 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380839] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001629 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8+ Natural Killer T Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001630 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8+ Natural Killer T %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001631 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8+ Natural Killer T %lymphocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001632 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8dim Natural Killer T Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001633 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8dim Natural Killer T %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001634 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD8dim Natural Killer T %lymphocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001635 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4-CD8- Natural Killer T Absolute Count 3,652 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427348] (imputed) 6 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001636 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4-CD8- Natural Killer T %T cell 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001637 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4-CD8- Natural Killer T %lymphocyte 3,668 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430788] (imputed) 6 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001638 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3- lymphocyte Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001639 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3- lymphocyte %lymphocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001640 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD3- lymphocyte %leukocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001641 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. B cell Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001642 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. B cell %CD3- lymphocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001643 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. B cell %lymphocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001644 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Natural Killer Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001645 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Natural Killer %CD3- lymphocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001646 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Natural Killer %lymphocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001647 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ Natural Killer Absolute Count 3,580 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18377392] (imputed) 3 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001648 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ Natural Killer %Natural Killer 3,596 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380873] (imputed) 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001649 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. HLA DR+ Natural Killer %CD3- lymphocyte 3,596 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18380873] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001650 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Granulocyte Absolute Count 3,653 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18427377] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001651 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Granulocyte %leukocyte 3,669 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18430820] (imputed) 2 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90001652 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ B cell %B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238340] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001391 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38+ B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001392 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38dim B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001393 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38dim B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001394 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38- B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001395 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38- B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001396 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Unswitched memory B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001397 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Unswitched memory B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001398 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD27- B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001399 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ B cell Absolute Count 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238316] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001400 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD27- B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001401 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Switched memory B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001402 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Switched memory B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001403 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Plasma Blast-Plasma Cell %B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238642] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001404 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Plasma Blast-Plasma Cell Absolute Count 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238619] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001405 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Memory B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001406 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Memory B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001407 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive-mature B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001408 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive-mature B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001409 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38+ B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001410 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD24+ B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001411 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD24+ B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001412 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD24- B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001413 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD24- B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001414 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD24- B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001415 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD24- B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001416 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24+ CD27+ B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001417 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24+ CD27+ B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001418 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20- B cell %B cell 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238340] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001419 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38+ B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001420 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20- B cell Absolute Count 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238316] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001421 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20- CD38- B cell %B cell 3,659 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238368] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001422 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20- CD38- B cell Absolute Count 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238344] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001423 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ B cell %Lymphocyte 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238316] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001424 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38+ B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001425 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38dim B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001426 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38- B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001427 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38dim B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001428 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38+ B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001429 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38dim B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001430 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38- B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001431 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Unswitched memory B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001432 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD27- B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 2 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001433 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Switched memory B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001434 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Plasma Blast-Plasma Cell %lymphocyte 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238619] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001435 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Memory B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001436 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. Naive-mature B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001437 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38dim B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001438 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD24+ B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001439 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD24- B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001440 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD24- B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001441 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD24+ CD27+ B cell %lymphocyte 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001442 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20- B cell %lymphocyte 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238316] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001443 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1277) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006130 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1278) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006131 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1279) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006132 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1280) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006133 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1281) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006134 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1282) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006135 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1283) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006136 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1284) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006137 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1285) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006138 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1286) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006139 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1287) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006140 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1288) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006141 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1289) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006142 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1290) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006143 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1291) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006144 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1292) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006145 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1293) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006146 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1294) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006147 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1295) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006148 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1296) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006149 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1297) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006150 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1298) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006151 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1299) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006152 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1300) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006153 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1301) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006154 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1302) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006155 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1303) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006156 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1304) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006157 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1305) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006158 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1306) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006159 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1307) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006160 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1308) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006161 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1309) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006162 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1310) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006163 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1311) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006164 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1312) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006165 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1313) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006166 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1314) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006167 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1315) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006168 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1316) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006169 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1317) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006170 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1318) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006171 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1319) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006172 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1320) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006173 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1321) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006174 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1322) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006175 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1323) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006176 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1324) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006177 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1325) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006178 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1326) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006179 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1327) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006180 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1328) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006181 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1329) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006182 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1330) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006183 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1331) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006184 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1332) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006185 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1333) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006186 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1334) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006187 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1335) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006188 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1336) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006189 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1337) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006190 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1338) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006191 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1339) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006192 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1340) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006193 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1341) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006194 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1342) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006195 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1343) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006196 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1344) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006197 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1345) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006198 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1346) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006199 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1347) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006200 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1348) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006201 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1349) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006202 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1350) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006203 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1351) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006204 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1352) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006205 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1353) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006206 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1354) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006207 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1355) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006208 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1356) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006209 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1357) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006210 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1358) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006211 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1359) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006212 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1360) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006213 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1361) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006214 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1362) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006215 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1363) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006216 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1364) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006217 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1365) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006218 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1366) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006219 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1367) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006220 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1368) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006221 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1369) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006222 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1370) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006223 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1371) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006224 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1372) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006225 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1373) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006226 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1374) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006227 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1375) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006228 Genome-wide genotyping array 2022-05-31 33875891 Smith SM 2021-04-19 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/33875891 An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank. rfMRI connectivity (ICA100 edge 1376) 21,081 British ancestry individuals 10,607 British ancestry individuals Affymetrix [17103079] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90006229 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD20- CD38- B cell %lymphocyte 3,658 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238344] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001444 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38- B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001445 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD- CD38- B cell Absolute Count 3,656 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238287] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001446 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. IgD+ CD38+ B cell %B cell 3,657 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18238311] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001447 Genome-wide genotyping array 2022-02-14 32929287 Orru V 2020-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/32929287 Complex genetic signatures in immune cells underlie autoimmunity and inform therapy. CD4 regulatory T cell %CD4+ T cell 3,437 Sardinian (founder/genetic isolate) ancestry individuals NA Illumina [18353565] (imputed) 1 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90001478 Genome-wide genotyping array 2020-11-26 32561361 Innes H 2020-06-16 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/32561361 Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. Forns index in high alcohol intake 33,437 British ancestry individuals NA NR [6200000] (imputed) 46 liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0010576 GCST90011734 Genome-wide genotyping array 2020-11-26 32561361 Innes H 2020-06-16 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/32561361 Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. Aspartate aminotransferase platelet ratio index in high alcohol intake 33,330 British ancestry individuals NA NR [6200000] (imputed) 46 liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0010576 GCST90011735 Genome-wide genotyping array 2020-11-26 32561361 Innes H 2020-06-16 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/32561361 Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. Fibrosis-4 index in high alcohol intake 33,324 British ancestry individuals NA NR [6200000] (imputed) 43 liver fibrosis measurement http://www.ebi.ac.uk/efo/EFO_0010576 GCST90011736 Genome-wide genotyping array 2020-11-26 32561361 Innes H 2020-06-16 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/32561361 Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. Aspartate transaminase levels in high alcohol intake 34,101 British ancestry individuals NA NR [6200000] (imputed) 12 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90011737 Genome-wide genotyping array 2020-11-26 32561361 Innes H 2020-06-16 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/32561361 Genome-wide Association Study for Alcohol-related Cirrhosis Identifies Risk Loci in MARC1 and HNRNPUL1. Alanine transaminase levels in high alcohol intake 34,238 British ancestry individuals NA NR [6200000] (imputed) 17 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90011738 Genome-wide genotyping array 2022-01-19 33574277 Kawai Y 2021-02-11 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/33574277 Mapping of susceptible variants for cold medicine-related Stevens-Johnson syndrome by whole-genome resequencing. Cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis (SJS/TEN) with severe ocular complications 133 Japanese ancestry cases, 418 Japanese ancestry controls NA Illumina [7608150] 25 Stevens-Johnson syndrome, toxic epidermal necrolysis, response to cold medicine http://www.ebi.ac.uk/efo/EFO_0004276, http://www.ebi.ac.uk/efo/EFO_0004775, http://www.ebi.ac.uk/efo/EFO_0006997 GCST90093113 Genome-wide sequencing 2021-03-22 29228018 Roos TR 2017-12-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/29228018 Genome-wide association study identifies a locus associated with rotator cuff injury. Rotator cuff injury 6,993 European ancestry cases, 669 Latin American cases, 394 East Asian ancestry cases, 269 African American cases, 32 South Asian ancestry cases, 76,271 European ancestry controls, 7,891 Latin American controls, 7,124 East Asian ancestry controls, 2,892 African American controls, 444 South Asian ancestry controls NA Affymetrix [10582947] (imputed) 1 rotator cuff tear http://www.ebi.ac.uk/efo/EFO_1001250 GCST011374 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. C-X-C motif chemokine 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 chemokine (C-X-C motif) ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0008083 GCST90012019 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Lectin-like oxidized LDL receptor 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 lectin-like oxidized LDL receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010918 GCST90012020 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. TNF-related apoptosis-inducing ligand receptor 2 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 6 TNF-related apoptosis-inducing ligand receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0010930 GCST90012021 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Fibroblast growth factor 23 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 7 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90012022 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Stem cell factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 17 stem Cell Factor measurement http://www.ebi.ac.uk/efo/EFO_0008291 GCST90012023 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Interleukin-18 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 10 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST90012024 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Interleukin-6 receptor subunit alpha levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90012025 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Tumor necrosis factor receptor 2 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 7 tumor necrosis factor receptor II measurement http://www.ebi.ac.uk/efo/EFO_0008384 GCST90012026 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Matrix metalloproteinase-3 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 7 matrix metalloproteinase measurement http://www.ebi.ac.uk/efo/EFO_0004744 GCST90012027 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Heat shock 27 kDa protein levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 heat shock 27 kDa protein measurement http://www.ebi.ac.uk/efo/EFO_0010915 GCST90012028 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Tumor necrosis factor ligand superfamily member 14 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90012029 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Prolactin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 0 prolactin measurement http://www.ebi.ac.uk/efo/EFO_0007003 GCST90012030 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Myeloperoxidase levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 11 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90012031 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Growth hormone levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 0 growth hormone measurement http://www.ebi.ac.uk/efo/EFO_0008438 GCST90012032 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Matrix metalloproteinase-1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 9 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90012033 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Resistin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 15 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90012034 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Tumor necrosis factor receptor superfamily member 6 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90012035 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Pappalysin-1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 13 pappalysin‐1 measurement http://www.ebi.ac.uk/efo/EFO_0010618 GCST90012036 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Pentraxin-related protein PTX3 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 6 pentraxin-related protein PTX3 measurement http://www.ebi.ac.uk/efo/EFO_0010923 GCST90012037 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Renin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 5 renin measurement http://www.ebi.ac.uk/efo/EFO_0010616 GCST90012038 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Chitinase-3-like protein 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 5 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90012039 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. ST2 protein levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 10 ST2 protein measurement http://www.ebi.ac.uk/efo/EFO_0010599 GCST90012040 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Kidney injury molecule 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 10 kidney injury molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010917 GCST90012041 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. beta-nerve growth factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 0 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST90012042 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Membrane-bound aminopeptidase P levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 membrane-bound aminopeptidase P measurement http://www.ebi.ac.uk/efo/EFO_0010920 GCST90012043 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. TNF-related activation-induced cytokine levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 7 TNF-related activation-induced cytokine measurement http://www.ebi.ac.uk/efo/EFO_0010929 GCST90012044 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Hepatocyte growth factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90012045 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. P-selectin glycoprotein ligand 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 P-selectin glycoprotein ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0010922 GCST90012046 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Myoglobin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 myoglobin measurement http://www.ebi.ac.uk/efo/EFO_0005057 GCST90012047 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Thrombomodulin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 5 thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0007774 GCST90012048 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Pro-interleukin-16 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 10 pro‐interleukin‐16 measurement http://www.ebi.ac.uk/efo/EFO_0010629 GCST90012049 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Matrix metalloproteinase-10 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 6 matrix metalloproteinase 10 measurement http://www.ebi.ac.uk/efo/EFO_0010589 GCST90012050 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Urokinase plasminogen activator surface receptor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90012051 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. C-C motif chemokine 4 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 CCL4 measurement http://www.ebi.ac.uk/efo/EFO_0004751 GCST90012052 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Cathepsin D levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 cathepsin D measurement http://www.ebi.ac.uk/efo/EFO_0010611 GCST90012053 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Receptor for advanced glycosylation end products levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 14 advanced glycosylation end product-specific receptor ligand measurement http://www.ebi.ac.uk/efo/EFO_0010762 GCST90012054 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. C-C motif chemokine 3 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 6 C-C motif chemokine 3 measurement http://www.ebi.ac.uk/efo/EFO_0008051 GCST90012055 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Matrix metalloproteinase-7 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 6 matrix metalloproteinase 7 measurement http://www.ebi.ac.uk/efo/EFO_0010591 GCST90012056 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. C-X-C motif chemokine 6 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90012057 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Melusin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 1 melusin measurement http://www.ebi.ac.uk/efo/EFO_0010919 GCST90012058 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. C-X-C motif chemokine 16 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 14 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90012059 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Dickkopf-related protein 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 9 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90012060 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. SIR2-like protein 2 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 SIR2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0010928 GCST90012061 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Galanin peptide levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 galanin peptides measurement http://www.ebi.ac.uk/efo/EFO_0010615 GCST90012062 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Agouti-related protein levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 5 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90012063 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Protein S100-A12 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 0 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90012064 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Tumor necrosis factor receptor superfamily member 5 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 tumor necrosis factor, receptor superfamily, member 5 measurement http://www.ebi.ac.uk/efo/EFO_0010607 GCST90012065 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Tissue-type plasminogen activator levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 tissue plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0004791 GCST90012066 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Proheparin-binding EGF-like growth factor levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 7 proheparin-binding EGF-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010924 GCST90012067 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Endothelial cell-specific molecule 1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 endothelial cell-specific molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010912 GCST90012068 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. vascular endothelial growth factor D levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90012069 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Matrix metalloproteinase-12 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 6 matrix metalloproteinase 12 measurement http://www.ebi.ac.uk/efo/EFO_0010590 GCST90012070 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Spondin-1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 3 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90012071 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Caspase 8 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 caspase-8 measurement http://www.ebi.ac.uk/efo/EFO_0010764 GCST90012072 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Cathepsin L1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 12 cathepsin L1 measurement http://www.ebi.ac.uk/efo/EFO_0010619 GCST90012073 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. CX3CL1 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 5 CX3CL1 measurement http://www.ebi.ac.uk/efo/EFO_0009419 GCST90012074 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Fatty acid-binding protein, adipocyte levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 4 fatty acid-binding protein, adipocyte measurement http://www.ebi.ac.uk/efo/EFO_0010914 GCST90012075 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. circulating leptin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90012076 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. C-C motif chemokine 20 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 C-C motif chemokine 20 measurement http://www.ebi.ac.uk/efo/EFO_0010910 GCST90012077 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Ovarian cancer-related tumor marker CA 125 levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 8 cancer antigen 125 measurement http://www.ebi.ac.uk/efo/EFO_0010603 GCST90012078 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. NF-kappa-B essential modulator levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 0 NF-kappa-B essential modulator measurement http://www.ebi.ac.uk/efo/EFO_0010597 GCST90012079 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Follistatin levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 6 follistatin measurement http://www.ebi.ac.uk/efo/EFO_0010614 GCST90012080 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Platelet endothelial cell adhesion molecule levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 2 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90012081 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. N-terminal prohormone brain natriuretic peptide levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 1 N-terminal prohormone brain natriuretic peptide measurement http://www.ebi.ac.uk/efo/EFO_0010921 GCST90012082 Genome-wide genotyping array 2020-11-24 33067605 Folkersen L 2020-10-16 Nat Metab www.ncbi.nlm.nih.gov/pubmed/33067605 Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals. Eosinophil cationic protein levels 21,758 European ancestry individuals 9,173 individuals Affymetrix, Illumina [20300000] (imputed) 1 eosinophil cationic protein measurement http://www.ebi.ac.uk/efo/EFO_0010913 GCST90012083 Genome-wide genotyping array 2022-01-14 34957435 Bonfiglio F 2021-12-08 Cell Genom www.ncbi.nlm.nih.gov/pubmed/34957435 GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome. Stool frequency 167,875 European ancestry individuals NA Affymetrix, Illumina [8817117] (imputed) 14 bowel opening frequency http://www.ebi.ac.uk/efo/EFO_0600084 GCST90002250 Genome-wide genotyping array 2022-01-14 34957435 Bonfiglio F 2021-12-08 Cell Genom www.ncbi.nlm.nih.gov/pubmed/34957435 GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome. Stool frequency 70,998 European ancestry men NA Affymetrix [8817117] (imputed) 1 bowel opening frequency http://www.ebi.ac.uk/efo/EFO_0600084 GCST012638 Genome-wide genotyping array 2022-01-14 34957435 Bonfiglio F 2021-12-08 Cell Genom www.ncbi.nlm.nih.gov/pubmed/34957435 GWAS of stool frequency provides insights into gastrointestinal motility and irritable bowel syndrome. Stool frequency 92,618 European ancestry women NA Affymetrix [8817117] (imputed) 2 bowel opening frequency http://www.ebi.ac.uk/efo/EFO_0600084 GCST012637 Genome-wide genotyping array 2021-05-28 33144568 Quach BC 2020-11-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33144568 Expanding the genetic architecture of nicotine dependence and its shared genetics with multiple traits. Nicotine dependence 46,213 European ancestry individuals, 11,787 African American individuals 31,854 European ancestry individuals, 1,937 individuals Affymetrix, Illumina [NR] (imputed) 7 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST011754 Genome-wide genotyping array 2021-02-03 33218114 Rebelo MA 2020-11-18 Brain Sci www.ncbi.nlm.nih.gov/pubmed/33218114 Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band. Beta 1 electroencephalogram power 191 European ancestry individuals NA Affymetrix [388620] 4 beta wave measurement http://www.ebi.ac.uk/efo/EFO_0006871 GCST011043 Genome-wide genotyping array 2021-02-03 33218114 Rebelo MA 2020-11-18 Brain Sci www.ncbi.nlm.nih.gov/pubmed/33218114 Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band. Beta 2 electroencephalogram power 191 European ancestry individuals NA Affymetrix [388620] 4 beta wave measurement http://www.ebi.ac.uk/efo/EFO_0006871 GCST011042 Genome-wide genotyping array 2021-02-03 33218114 Rebelo MA 2020-11-18 Brain Sci www.ncbi.nlm.nih.gov/pubmed/33218114 Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band. Delta electroencephalogram power 191 European ancestry individuals NA Affymetrix [388620] 1 delta wave measurement http://www.ebi.ac.uk/efo/EFO_0006872 GCST011041 Genome-wide genotyping array 2021-02-03 33218114 Rebelo MA 2020-11-18 Brain Sci www.ncbi.nlm.nih.gov/pubmed/33218114 Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band. Theta electroencephalogram power 191 European ancestry individuals NA Affymetrix [388620] 7 theta wave measurement http://www.ebi.ac.uk/efo/EFO_0006873 GCST011040 Genome-wide genotyping array 2021-02-03 33218114 Rebelo MA 2020-11-18 Brain Sci www.ncbi.nlm.nih.gov/pubmed/33218114 Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band. Alpha electroencephalogram power 191 European ancestry individuals NA Affymetrix [388620] 2 alpha wave measurement http://www.ebi.ac.uk/efo/EFO_0006870 GCST011044 Genome-wide genotyping array 2021-07-27 33409738 Abdel-Wahab N 2021-01-07 Cancer Immunol Immunother www.ncbi.nlm.nih.gov/pubmed/33409738 Genetic determinants of immune-related adverse events in patients with melanoma receiving immune checkpoint inhibitors. Response to immune checkpoint inhibitors in melanoma (immune-related adverse events) 43 European ancestry cases, 1 case, 42 European ancestry controls, 1 African ancestry control, 2 controls NA Illumina [599931] 4 response to immune checkpoint inhibitor, immune system toxicity http://www.ebi.ac.uk/efo/EFO_0600023, http://www.ebi.ac.uk/efo/EFO_0011053 GCST012118 Genome-wide genotyping array 2021-03-22 33290408 Ray D 2020-12-08 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33290408 A powerful method for pleiotropic analysis under composite null hypothesis identifies novel shared loci between Type 2 Diabetes and Prostate Cancer. Type 2 diabetes or prostate cancer (pleiotropy) 62,892 European ancestry T2D cases, 79,194 European ancestry PrCa cases, 659,536 European ancestry controls NA Illumina [5041948] (imputed) 43 prostate carcinoma, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0001663, http://purl.obolibrary.org/obo/MONDO_0005148 GCST011320 Genome-wide genotyping array 2021-09-08 33832965 Sandoval-Plata G 2021-04-08 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33832965 Variants in urate transporters, ADH1B, GCKR and MEPE genes associate with transition from asymptomatic hyperuricaemia to gout: results of the first gout versus asymptomatic hyperuricaemia GWAS in Caucasians using data from the UK Biobank. Gout 7,049 European ancestry cases, 64,424 European ancestry controls NA Affymetrix [710030] 34 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST012338 Genome-wide genotyping array 2021-09-08 33832965 Sandoval-Plata G 2021-04-08 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33832965 Variants in urate transporters, ADH1B, GCKR and MEPE genes associate with transition from asymptomatic hyperuricaemia to gout: results of the first gout versus asymptomatic hyperuricaemia GWAS in Caucasians using data from the UK Biobank. Gout vs asymptomatic hyperuricemia 4,934 European ancestry cases, 56,948 European ancestry controls 2,115 European ancestry cases, 24,406 European ancestry controls Affymetrix [710030] 13 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST012339 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Angina (UKB data field 6150) 14,103 European ancestry cases, 115,540 European ancestry controls NA Affymetrix, Illumina [226621] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90079443 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oral diabetes medication use (Gene-based burden) 13,132 European ancestry cases, 307,626 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90085489 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart attack (UKB data field 6150) 10,286 European ancestry cases, 119,357 European ancestry controls NA Affymetrix, Illumina [226621] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90079442 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other eye problems (UKB data field 2227) (Gene-based burden) 68,925 European ancestry cases, 360,799 European ancestry controls NA Illumina [185934] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90082856 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High blood pressure (UKB data field 6150) 117,747 European ancestry cases, 11,896 European ancestry controls NA Affymetrix, Illumina [226621] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90079445 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall acceleration average (UKB data field 90012) (Gene-based burden) 91,770 European ancestry individuals NA Illumina [161846] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083492 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stroke (UKB data field 6150) 6,774 European ancestry cases, 122,869 European ancestry controls NA Affymetrix, Illumina [226621] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90079444 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Excellent (UKB data field 2178) (Gene-based burden) 75,468 European ancestry cases, 353,648 European ancestry controls NA Illumina [185926] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082832 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Daily or almost daily (UKB data field 20416) 4,457 European ancestry cases, 123,692 European ancestry controls NA Affymetrix, Illumina [224880] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078436 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Fair (UKB data field 2178) (Gene-based burden) 93,192 European ancestry cases, 335,924 European ancestry controls NA Illumina [185926] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082834 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Less than monthly (UKB data field 20416) 31,416 European ancestry cases, 96,733 European ancestry controls NA Affymetrix, Illumina [224880] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078433 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Good (UKB data field 2178) (Gene-based burden) 258,685 European ancestry cases, 170,431 European ancestry controls NA Illumina [185926] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082833 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Monthly (UKB data field 20416) 11,334 European ancestry cases, 116,815 European ancestry controls NA Affymetrix, Illumina [224880] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078434 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall health rating - Poor (UKB data field 2178) (Gene-based burden) 19,322 European ancestry cases, 409,794 European ancestry controls NA Illumina [185926] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082835 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Never (UKB data field 20416) 64,157 European ancestry cases, 63,992 European ancestry controls NA Affymetrix, Illumina [224880] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078432 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pace maker (UKB data field 3079) (Gene-based burden) 1,415 European ancestry cases, 429,190 European ancestry controls NA Illumina [185945] 0 artificial cardiac pacemaker http://www.ebi.ac.uk/efo/EFO_0009719 GCST90083021 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Weekly (UKB data field 20416) 16,785 European ancestry cases, 111,364 European ancestry controls NA Affymetrix, Illumina [224880] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078435 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pack years adult smoking as proportion of life span exposed to smoking (UKB data field 20162) (Gene-based burden) 134,156 European ancestry individuals NA Illumina [171773] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082312 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 10 or more (UKB data field 20403) 3,660 European ancestry cases, 124,233 European ancestry controls NA Affymetrix, Illumina [224469] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078401 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pack years of smoking (UKB data field 20161) (Gene-based burden) 134,156 European ancestry individuals NA Illumina [171773] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082311 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 1 or 2 (UKB data field 20403) 65,330 European ancestry cases, 62,563 European ancestry controls NA Affymetrix, Illumina [224469] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078397 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Back pain (UKB data field 6159) (Gene-based burden) 116,024 European ancestry cases, 149,919 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083467 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 3 or 4 (UKB data field 20403) 35,084 European ancestry cases, 92,809 European ancestry controls NA Affymetrix, Illumina [224469] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078398 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Facial pain (UKB data field 6159) (Gene-based burden) 8,530 European ancestry cases, 257,413 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083465 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 5 or 6 (UKB data field 20403) 15,507 European ancestry cases, 112,386 European ancestry controls NA Affymetrix, Illumina [224469] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078399 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent changes in speed amount of moving or speaking - Several days (UKB data field 20518) (Gene-based burden) 5,978 European ancestry cases, 133,494 European ancestry controls NA Illumina [172116] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90082588 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cough on most days (UKB data field 22502) 14,729 European ancestry cases, 93,520 European ancestry controls NA Affymetrix, Illumina [195823] 0 Cough http://purl.obolibrary.org/obo/HP_0012735 GCST90078872 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent easy annoyance or irritability - More than half the days (UKB data field 20505) (Gene-based burden) 2,811 European ancestry cases, 136,216 European ancestry controls NA Illumina [172018] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90082546 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma (UKB data field 22127) 13,735 European ancestry cases, 94,514 European ancestry controls NA Affymetrix, Illumina [195823] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90078862 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent easy annoyance or irritability - Nearly every day (UKB data field 20505) (Gene-based burden) 2,044 European ancestry cases, 136,983 European ancestry controls NA Illumina [172018] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90082547 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bronchiectasis (UKB data field 22134) 947 European ancestry cases, 107,302 European ancestry controls NA Affymetrix, Illumina [195823] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90078865 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent easy annoyance or irritability - Several days (UKB data field 20505) (Gene-based burden) 33,713 European ancestry cases, 105,314 European ancestry controls NA Illumina [172018] 0 behavior or behavioral disorder measurement http://www.ebi.ac.uk/efo/EFO_0004782 GCST90082545 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic bronchitis (UKB data field 22129) 1,225 European ancestry cases, 107,024 European ancestry controls NA Affymetrix, Illumina [195823] 0 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST90078863 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of depression - More than half the days (UKB data field 20510) (Gene-based burden) 2,823 European ancestry cases, 136,410 European ancestry controls NA Illumina [172077] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082564 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease (UKB data field 22130) 1,566 European ancestry cases, 106,683 European ancestry controls NA Affymetrix, Illumina [195823] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90078864 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of depression - Nearly every day (UKB data field 20510) (Gene-based burden) 1,965 European ancestry cases, 137,268 European ancestry controls NA Illumina [172077] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082565 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hayfever or rhinitis (UKB data field 22126) 24,550 European ancestry cases, 83,699 European ancestry controls NA Affymetrix, Illumina [195823] 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90078861 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of depression - Several days (UKB data field 20510) (Gene-based burden) 26,550 European ancestry cases, 112,683 European ancestry controls NA Illumina [172077] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082563 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tuberculosis (UKB data field 22137) 574 European ancestry cases, 107,675 European ancestry controls NA Affymetrix, Illumina [195822] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90078866 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of foreboding - More than half the days (UKB data field 20512) (Gene-based burden) 2,372 European ancestry cases, 136,661 European ancestry controls NA Illumina [172012] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082570 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism angle right (UKB data field 5088) 107,475 European ancestry individuals NA Affymetrix, Illumina [195236] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90079271 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of foreboding - Nearly every day (UKB data field 20512) (Gene-based burden) 2,447 European ancestry cases, 136,586 European ancestry controls NA Illumina [172012] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082571 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - Cylindrical power right (UKB data field 5087) 107,475 European ancestry individuals NA Affymetrix, Illumina [195236] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079270 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of foreboding - Several days (UKB data field 20512) (Gene-based burden) 18,747 European ancestry cases, 120,286 European ancestry controls NA Illumina [172012] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082569 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical power right (UKB data field 5084) 107,475 European ancestry individuals NA Affymetrix, Illumina [195236] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079267 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of inadequacy - More than half the days (UKB data field 20507) (Gene-based burden) 3,036 European ancestry cases, 136,011 European ancestry controls NA Illumina [172067] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082552 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent right 107,475 European ancestry individuals NA Affymetrix, Illumina [195236] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081512 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of inadequacy - Nearly every day (UKB data field 20507) (Gene-based burden) 2,929 European ancestry cases, 136,118 European ancestry controls NA Illumina [172067] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082553 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking in former smokers (age of onset) (UKB data field 2867) 108,465 European ancestry individuals NA Affymetrix, Illumina [195188] 0 smoking status measurement, age at onset http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90078965 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of inadequacy - Several days (UKB data field 20507) (Gene-based burden) 21,459 European ancestry cases, 117,588 European ancestry controls NA Illumina [172067] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082551 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Headache (UKB data field 6159) (Gene-based burden) 89,640 European ancestry cases, 176,303 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083464 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amount of alcoholic units drunk on a typical drinking day - 7, 8 or 9 (UKB data field 20403) 8,312 European ancestry cases, 119,581 European ancestry controls NA Affymetrix, Illumina [224469] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90078400 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Hip pain (UKB data field 6159) (Gene-based burden) 52,712 European ancestry cases, 213,231 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083469 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - break (UKB data field 5001) 1,234 European ancestry cases, 125,748 European ancestry controls NA Affymetrix, Illumina [223837] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079258 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Knee pain (UKB data field 6159) (Gene-based burden) 98,206 European ancestry cases, 167,737 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083470 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - cease (UKB data field 5001) 112,537 European ancestry cases, 14,445 European ancestry controls NA Affymetrix, Illumina [223837] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079257 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Neck or shoulder pain (UKB data field 6159) (Gene-based burden) 104,510 European ancestry cases, 161,433 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083466 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - close (UKB data field 5001) 2,049 European ancestry cases, 124,933 European ancestry controls NA Affymetrix, Illumina [223837] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079256 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Pain all over the body (UKB data field 6159) (Gene-based burden) 7,206 European ancestry cases, 258,737 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083471 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - pause (UKB data field 5001) 11,287 European ancestry cases, 115,695 European ancestry controls NA Affymetrix, Illumina [223837] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079255 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pain types experienced in last month - Stomach or abdominal pain (UKB data field 6159) (Gene-based burden) 38,802 European ancestry cases, 227,141 European ancestry controls NA Illumina [182279] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083468 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - rest (UKB data field 5001) 1,461 European ancestry cases, 125,521 European ancestry controls NA Affymetrix, Illumina [223837] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079259 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching completion status - Abandoned (UKB data field 20244) (Gene-based burden) 3,284 European ancestry cases, 102,117 European ancestry controls NA Illumina [165792] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082365 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - glyceryl trinitrate (Gene-based burden) 1,422 European ancestry cases, 319,336 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081986 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Wrist (UKB data field 6151) 9,426 European ancestry cases, 35,767 European ancestry controls NA Affymetrix, Illumina [91068] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90079450 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gtn spray (Gene-based burden) 1,101 European ancestry cases, 319,657 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081980 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression possibly related to childbirth (UKB data field 20445) 5,752 European ancestry cases, 39,705 European ancestry controls NA Affymetrix, Illumina [91033] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078466 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - gtn glyceryl trinitrate (Gene-based burden) 776 European ancestry cases, 319,982 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082149 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 1 (UKB data field 21036) 4,633 European ancestry cases, 40,308 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078733 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - hydrocortisone (Gene-based burden) 842 European ancestry cases, 319,916 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082061 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 2 (UKB data field 21036) 8,224 European ancestry cases, 36,717 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078734 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - hydroxychloroquine (Gene-based burden) 691 European ancestry cases, 320,067 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082099 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 3 (UKB data field 21036) 7,955 European ancestry cases, 36,986 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078735 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - hypromellose (Gene-based burden) 808 European ancestry cases, 319,950 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082064 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 4 (UKB data field 21036) 4,900 European ancestry cases, 40,041 European ancestry controls NA Affymetrix, Illumina [90486] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078736 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lercanidipine (Gene-based burden) 1,219 European ancestry cases, 319,539 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082171 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 7 days with pain (UKB data field 21037) 1,828 European ancestry cases, 42,866 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078750 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - levothyroxine sodium (Gene-based burden) 19,017 European ancestry cases, 301,741 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082210 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 8 days with pain (UKB data field 21037) 1,632 European ancestry cases, 43,062 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078751 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lipitor (Gene-based burden) 3,244 European ancestry cases, 317,514 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082161 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of days out of 10 with abdominal pain - 9 days with pain (UKB data field 21037) 929 European ancestry cases, 43,765 European ancestry controls NA Affymetrix, Illumina [90006] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078752 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - lisinopril (Gene-based burden) 12,532 European ancestry cases, 308,226 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081984 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression (UKB data field 20544) 29,907 European ancestry cases, 14,440 European ancestry controls NA Affymetrix, Illumina [89370] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078637 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - livial (Gene-based burden) 594 European ancestry cases, 320,164 European ancestry controls NA Illumina [183953] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082091 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anxiety, nerves or generalized anxiety disorder (UKB data field 20544) 19,743 European ancestry cases, 24,570 European ancestry controls NA Affymetrix, Illumina [89302] 0 generalized anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001892 GCST90078639 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - loperamide (Gene-based burden) 1,496 European ancestry cases, 319,262 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082072 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Panic attacks (UKB data field 20544) 7,804 European ancestry cases, 36,479 European ancestry controls NA Affymetrix, Illumina [89251] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90078645 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - loratadine (Gene-based burden) 3,386 European ancestry cases, 317,372 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082006 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Social anxiety or social phobia (UKB data field 20544) 1,734 European ancestry cases, 42,543 European ancestry controls NA Affymetrix, Illumina [89235] 0 social anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001917 GCST90078642 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - losartan (Gene-based burden) 4,692 European ancestry cases, 316,066 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082136 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Obsessive compulsive disorder (UKB data field 20544) 866 European ancestry cases, 43,403 European ancestry controls NA Affymetrix, Illumina [89224] 0 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST90078646 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mebeverine (Gene-based burden) 2,282 European ancestry cases, 318,476 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082070 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mania, hypomania, bipolar or manic depression (UKB data field 20544) 733 European ancestry cases, 43,534 European ancestry controls NA Affymetrix, Illumina [89219] 0 mood disorder http://www.ebi.ac.uk/efo/EFO_0004247 GCST90078636 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - meloxicam (Gene-based burden) 1,254 European ancestry cases, 319,504 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082154 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Any other phobia e.g. disabling fear of heights or spiders (UKB data field 20544) 1,902 European ancestry cases, 42,366 European ancestry controls NA Affymetrix, Illumina [89217] 0 specific phobia http://www.ebi.ac.uk/efo/EFO_1001918 GCST90078644 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - mesalazine (Gene-based burden) 645 European ancestry cases, 320,113 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082016 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anorexia nervosa (UKB data field 20544) 781 European ancestry cases, 43,483 European ancestry controls NA Affymetrix, Illumina [89214] 0 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST90078640 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - metformin (Gene-based burden) 11,579 European ancestry cases, 309,179 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082105 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Any other type of psychosis or psychotic illness (UKB data field 20544) 526 European ancestry cases, 43,738 European ancestry controls NA Affymetrix, Illumina [89213] 0 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST90078643 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bring up phlegm sputum mucus on most days (UKB data field 22504) 9,287 European ancestry cases, 98,962 European ancestry controls NA Affymetrix, Illumina [195823] 0 bringing up phlegm, sputum or mucus on most days, self-reported http://www.ebi.ac.uk/efo/EFO_0009824 GCST90078873 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - final answer - Orange circle (UKB data field 4293) (Gene-based burden) 169,042 European ancestry cases, 6,841 European ancestry controls NA Illumina [176981] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90083160 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - Number of letters correct in round left (UKB data field 5077) 110,230 European ancestry individuals NA Affymetrix, Illumina [199357] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90079266 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - final answer - Pink star (UKB data field 4293) (Gene-based burden) 4,530 European ancestry cases, 171,353 European ancestry controls NA Illumina [176981] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90083158 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fluid intelligence completion status - Abandoned (UKB data field 20242) 3,187 European ancestry cases, 106,707 European ancestry controls NA Affymetrix, Illumina [198388] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078376 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - initial answer - Blue square (UKB data field 4292) (Gene-based burden) 36,948 European ancestry cases, 139,119 European ancestry controls NA Illumina [177002] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90083156 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fluid intelligence completion status - Completed (UKB data field 20242) 96,202 European ancestry cases, 13,692 European ancestry controls NA Affymetrix, Illumina [198388] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078375 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - initial answer - Orange circle (UKB data field 4292) (Gene-based burden) 141,954 European ancestry cases, 34,113 European ancestry controls NA Illumina [177002] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90083157 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fluid intelligence completion status - Completed with pause (UKB data field 20242) 10,505 European ancestry cases, 99,389 European ancestry controls NA Affymetrix, Illumina [198388] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078377 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Potassium in urine (UKB data field 30520) (Gene-based burden) 418,307 European ancestry individuals NA Illumina [185810] 0 urinary potassium measurement http://www.ebi.ac.uk/efo/EFO_0010952 GCST90082995 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Autorefraction - Duration at which refractometer first shown right (UKB data field 5190) 109,455 European ancestry individuals NA Affymetrix, Illumina [198269] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079327 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Previously smoked cigarettes on most/all days (UKB data field 5959) (Gene-based burden) 1,607 European ancestry cases, 779 European ancestry controls NA Illumina [28117] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90083389 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Autorefraction - Duration at which refractometer first shown left (UKB data field 5193) 109,455 European ancestry individuals NA Affymetrix, Illumina [198259] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079328 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Professional informed about anxiety (UKB data field 20428) (Gene-based burden) 26,395 European ancestry cases, 16,765 European ancestry controls NA Illumina [137917] 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90082431 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - logMAR final left (UKB data field 5208) 109,433 European ancestry individuals NA Affymetrix, Illumina [198215] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90079332 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Professional informed about depression (UKB data field 20448) (Gene-based burden) 50,878 European ancestry cases, 27,908 European ancestry controls NA Illumina [158015] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082455 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - logMAR final right (UKB data field 5201) 109,473 European ancestry individuals NA Affymetrix, Illumina [198153] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90079331 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - cycle rising to 50 level (UKB data field 6024) (Gene-based burden) 61,060 European ancestry cases, 20,643 European ancestry controls NA Illumina [160268] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083399 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 714 (UKB data field 20167) 828 European ancestry cases, 108,657 European ancestry controls NA Affymetrix, Illumina [197782] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078331 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - cycle rising to 35 level (UKB data field 6024) (Gene-based burden) 9,643 European ancestry cases, 72,060 European ancestry controls NA Illumina [160268] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083400 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 987 (UKB data field 20167) 108,555 European ancestry cases, 930 European ancestry controls NA Affymetrix, Illumina [197782] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078330 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - cycle at constant level (UKB data field 6024) (Gene-based burden) 2,320 European ancestry cases, 79,383 European ancestry controls NA Illumina [160268] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083401 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 14 (20165) 797 European ancestry cases, 108,689 European ancestry controls NA Affymetrix, Illumina [197769] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078327 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - at rest measurement (UKB data field 6024) (Gene-based burden) 8,201 European ancestry cases, 73,502 European ancestry controls NA Illumina [160268] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083402 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 15 (20165) 106,700 European ancestry cases, 2,786 European ancestry controls NA Affymetrix, Illumina [197769] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078328 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - No category, ECG not to be done (UKB data field 6024) (Gene-based burden) 1,253 European ancestry cases, 80,450 European ancestry controls NA Illumina [160268] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083403 Exome-wide sequencing 2018-06-11 29608535 Kuehn MH 2018-03-30 J Neuroophthalmol www.ncbi.nlm.nih.gov/pubmed/29608535 Genetic Survey of Adult-Onset Idiopathic Intracranial Hypertension. Idiopathic intracranial hypertension 63 European ancestry cases, 21 African American cases, 4 Native American cases, 1 Asian cases, 6 cases, 61 European ancestry controls, 21 African American controls, 3 Native American controls, 1 Asian controls, 9 controls NA Illumina [301908] 15 pseudotumor cerebri http://www.ebi.ac.uk/efo/EFO_1001132 GCST005688 Genome-wide genotyping array 2019-03-11 30760885 Mbarek H 2019-02-13 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30760885 Biological insights into multiple birth: genetic findings from UK Biobank. Number of twin births 8,962 European ancestry cases, 409,591 European ancestry controls NA Affymetrix [8532721] (imputed) 2 multiple births measurement http://www.ebi.ac.uk/efo/EFO_0009439 GCST007280 Genome-wide genotyping array 2018-12-03 30348214 Zhang Q 2018-10-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/30348214 Genotype effects contribute to variation in longitudinal methylome patterns in older people. DNA methylation variation (age effect) Up to 954 individuals NA Illumina [7760689] (imputed) 436 DNA methylation http://purl.obolibrary.org/obo/GO_0006306 GCST006660 Genome-wide genotyping array 2018-08-22 29860282 Scelsi MA 2018-05-30 Brain www.ncbi.nlm.nih.gov/pubmed/29860282 Genetic study of multimodal imaging Alzheimer's disease progression score implicates novel loci. Hippocampal volume 926 European ancestry individuals NA Illumina [5137218] (imputed) 13 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST006134 Genome-wide genotyping array 2018-08-22 29860282 Scelsi MA 2018-05-30 Brain www.ncbi.nlm.nih.gov/pubmed/29860282 Genetic study of multimodal imaging Alzheimer's disease progression score implicates novel loci. Cortical amyloid beta load 936 European ancestry individuals NA Illumina [5137218] (imputed) 15 cerebral amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0007707 GCST006135 Genome-wide genotyping array 2018-08-22 29860282 Scelsi MA 2018-05-30 Brain www.ncbi.nlm.nih.gov/pubmed/29860282 Genetic study of multimodal imaging Alzheimer's disease progression score implicates novel loci. Alzheimer's disease progression score 944 European ancestry individuals NA Illumina [5137218] (imputed) 13 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST006136 Genome-wide genotyping array 2018-10-17 29868124 Wu Y 2018-05-16 Front Genet www.ncbi.nlm.nih.gov/pubmed/29868124 Genetics of Obesity Traits: A Bivariate Genome-Wide Association Analysis. Body mass index and waist-hip ratio (pleiotropy) 139 Han Chinese ancestry dizygotic twin pairs NA Illumina [1365181] 8 waist-hip ratio, body mass index http://www.ebi.ac.uk/efo/EFO_0004343, http://www.ebi.ac.uk/efo/EFO_0004340 GCST006430 Genome-wide genotyping array 2019-07-30 30999091 Wang Y 2019-04-09 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/30999091 Post-traumatic stress following military deployment: Genetic associations and cross-disorder genetic correlations. Post-traumatic stress disorder symptoms in trauma-exposed soldiers 462 Danish ancestry cases, 2,019 Danish ancestry controls NA Illumina [NR] (imputed) 3 response to trauma exposure, post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008483, http://www.ebi.ac.uk/efo/EFO_0008535 GCST008270 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (drugs for peptic ulcer and gastro-oesophageal reflux disease) 53,137 European ancestry cases, 79,230 European ancestry controls NA Affymetrix [7288503] (imputed) 5 Peptic ulcer and gastro-oesophageal reflux disease (GORD) drug use measurement http://www.ebi.ac.uk/efo/EFO_0009923 GCST007922 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (drugs used in diabetes) 15,272 European ancestry cases, 29,0641 European ancestry controls NA Affymetrix [7288503] (imputed) 57 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST007923 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (antithrombotic agents) 67,653 European ancestry cases, 85,986 European ancestry controls NA Affymetrix [7288503] (imputed) 13 Antithrombotic agent use measurement http://www.ebi.ac.uk/efo/EFO_0009925 GCST007924 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (vasodilators used in cardiac diseases) 5,546 European ancestry cases, 237,113 European ancestry controls NA Affymetrix [7288503] (imputed) 3 Vasodilators used in cardiac diseases use measurement http://www.ebi.ac.uk/efo/EFO_0009926 GCST007925 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (antihypertensives) 6,431 European ancestry cases, 145,949 European ancestry controls NA Affymetrix [7288503] (imputed) 4 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST007926 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (diuretics) 34,453 European ancestry cases, 194,633 European ancestry controls NA Affymetrix [7288503] (imputed) 102 Diuretic use measurement http://www.ebi.ac.uk/efo/EFO_0009928 GCST007928 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (beta blocking agents) 31,700 European ancestry cases, 192,324 European ancestry controls NA Affymetrix [7288503] (imputed) 59 Beta blocking agent use measurement http://www.ebi.ac.uk/efo/EFO_0009929 GCST007927 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (calcium channel blockers) 31,904 European ancestry cases, 172,474 European ancestry controls NA Affymetrix [7288503] (imputed) 104 Calcium channel blocker use measurement http://www.ebi.ac.uk/efo/EFO_0009930 GCST007929 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (agents acting on the renin-angiotensin system) 62,752 European ancestry cases, 174,778 European ancestry controls NA Affymetrix [7288503] (imputed) 184 Agents acting on the renin-angiotensin system use measurement http://www.ebi.ac.uk/efo/EFO_0009931 GCST007930 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (HMG CoA reductase inhibitors) 73,475 European ancestry cases, 216,910 European ancestry controls NA Affymetrix [7288503] (imputed) 97 HMG CoA reductase inhibitor use measurement http://www.ebi.ac.uk/efo/EFO_0009932 GCST007931 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (thyroid preparations) 24,832 European ancestry cases, 280,750 European ancestry controls NA Affymetrix [7288503] (imputed) 132 Thyroid preparation use measurement http://www.ebi.ac.uk/efo/EFO_0009933 GCST007932 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (immunosuppressants) 3,954 European ancestry cases, 268,648 European ancestry controls NA Affymetrix [7288503] (imputed) 2 Immunosuppressant use measurement http://www.ebi.ac.uk/efo/EFO_0009934 GCST007933 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (anti-inflammatory and antirheumatic products, non-steroids) 74,150 European ancestry cases, 90,370 European ancestry controls NA Affymetrix [7288503] (imputed) 6 Non-steroidal anti-inflammatory and antirheumatic product use measurement http://www.ebi.ac.uk/efo/EFO_0009935 GCST007934 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (drugs affecting bone structure and mineralization) 7,870 European ancestry cases, 207,798 European ancestry controls NA Affymetrix [7288503] (imputed) 11 Drugs affecting bone structure and mineralization use measurement http://www.ebi.ac.uk/efo/EFO_0009936 GCST007935 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (opioids) 22,982 European ancestry cases, 55,826 European ancestry controls NA Affymetrix [7288503] (imputed) 3 Opioid use measurement http://www.ebi.ac.uk/efo/EFO_0009937 GCST007936 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (salicylic acid and derivatives) 61,583 European ancestry cases, 50,427 European ancestry controls NA Affymetrix [7288503] (imputed) 10 aspirin use measurement http://www.ebi.ac.uk/efo/EFO_0007013 GCST007937 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (anilides) 83,218 European ancestry cases, 96,592 European ancestry controls NA Affymetrix [7288503] (imputed) 7 Anilide use measurement http://www.ebi.ac.uk/efo/EFO_0009938 GCST007938 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (antimigraine preparations) 5,521 European ancestry cases, 114,323 European ancestry controls NA Affymetrix [7288503] (imputed) 13 Antimigraine preparation use measurement http://www.ebi.ac.uk/efo/EFO_0009939 GCST007939 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (antidepressants) 33,757 European ancestry cases, 270,405 European ancestry controls NA Affymetrix [7288503] (imputed) 1 Antidepressant use measurement http://www.ebi.ac.uk/efo/EFO_0009940 GCST007940 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (adrenergics, inhalants) 28,880 European ancestry cases, 147,565 European ancestry controls NA Affymetrix [7288503] (imputed) 56 Inhalant adrenergic use measurement http://www.ebi.ac.uk/efo/EFO_0009941 GCST007941 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (glucocorticoids) 17,352 European ancestry cases, 188,348 European ancestry controls NA Affymetrix [7288503] (imputed) 19 Glucocorticoid use measurement http://www.ebi.ac.uk/efo/EFO_0009942 GCST007942 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (antihistamines for systemic use) 13,984 European ancestry cases, 137,652 European ancestry controls NA Affymetrix [7288503] (imputed) 8 Antihistamine use measurement http://www.ebi.ac.uk/efo/EFO_0009943 GCST007943 Genome-wide genotyping array 2019-06-21 31015401 Wu Y 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015401 Genome-wide association study of medication-use and associated disease in the UK Biobank. Medication use (antiglaucoma preparations and miotics) 5,215 European ancestry cases, 95,653 European ancestry controls NA Affymetrix [7288503] (imputed) 14 Antiglaucoma preparations and miotics use measurement http://www.ebi.ac.uk/efo/EFO_0009944 GCST007944 Genome-wide genotyping array 2019-08-12 31235810 Fung K 2019-06-24 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31235810 Genome-wide association study identifies loci for arterial stiffness index in 127,121 UK Biobank participants. Arterial stiffness index 127,121 European ancestry individuals NA Affymetrix [~ 10446505] (imputed) 45 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST008403 Genome-wide genotyping array 2019-08-07 31206164 Richards AL 2019-06-17 Schizophr Bull (Bp) www.ncbi.nlm.nih.gov/pubmed/31206164 The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia. Cognitive ability in schizophrenia 3,034 European ancestry individuals NA Illumina [NR] (imputed) 3 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST008387 Genome-wide genotyping array 2019-08-10 31039275 Park SH 2019-04-30 J Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/31039275 Association of TRAP1 with Infliximab-Induced Mucosal Healing in Crohn's disease. Infliximab-induced mucosal healing in Crohn's disease 15 Korean ancestry responders, 43 Korean ancestry non-responders 27 Korean ancestry responders, 27 Korean ancestry non-responders NR [522285] 1 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST008397 Genome-wide genotyping array 2019-04-03 30373671 Hayden LP 2018-10-29 Respir Res www.ncbi.nlm.nih.gov/pubmed/30373671 Childhood asthma is associated with COPD and known asthma variants in COPDGene: a genome-wide association study. Self-reported childhood asthma in adult smokers 385 European ancestry cases, 4979 European ancestry controls, 325 African American cases, 2342 African American controls NA Illumina [up to 15374350] (imputed) 5 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST007508 Genome-wide genotyping array 2019-07-04 30998689 Shadrina AS 2019-04-18 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30998689 Varicose veins of lower extremities: Insights from the first large-scale genetic study. Varicose veins 10,861 British ancestry cases, 397,594 British ancestry controls NA Affymetrix [10829469] (imputed) 14 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST008057 Genome-wide genotyping array 2019-07-18 30929638 Matana A 2019-03-30 Thyroid www.ncbi.nlm.nih.gov/pubmed/30929638 Genetic variants in the ST6GAL1 gene are associated with thyroglobulin plasma level in healthy individuals. Thyroglobulin plasma levels 1,094 Croatian ancestry individuals NA Illumina [7597379] (imputed) 8 thyroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010050 GCST008170 Genome-wide genotyping array 2018-05-11 29596498 Charles BA 2018-03-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/29596498 Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia. Low white blood cell count 783 African American individuals with low white blood cell count, 1,214 African American individuals with high white blood cell count NA Affymetrix, Illumina [NR] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST005579 Genome-wide genotyping array 2018-05-11 29596498 Charles BA 2018-03-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/29596498 Analyses of genome wide association data, cytokines, and gene expression in African-Americans with benign ethnic neutropenia. Low white blood cell count (conditioned on rs2814778) 592 African American individuals with low white blood cell count, 586 African American individuals with high white blood cell count NA Illumina [at least 656747] (imputed) 16 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST005578 Genome-wide genotyping array 2020-01-23 31204042 Hou XH 2019-05-21 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/31204042 Genome-wide association study identifies Alzheimer's risk variant in MS4A6A influencing cerebrospinal fluid sTREM2 levels. Cerebrospinal fluid sTREM-2 levels 449 European ancestry individuals 377 Han Chinese ancestry individuals Illumina [3263912] (imputed) 1 soluble triggering receptor expressed on myeloid cells 2 measurement http://www.ebi.ac.uk/efo/EFO_0010151 GCST009476 Genome-wide genotyping array 2019-07-30 31043678 Aterido A 2019-05-02 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/31043678 Genetic association between CD96 locus and immunogenicity to anti-TNF therapy in Crohn's disease. Anti-adalimumab antibody production in response to treatment in Crohn's disease 9 European ancestry cases, 53 European ancestry controls 3 European ancestry cases, 85 European ancestry controls Illumina [540221] 1 response to TNF antagonist http://www.ebi.ac.uk/efo/EFO_0004653 GCST008271 Genome-wide genotyping array 2018-07-20 29884837 Reyes-Gibby CC 2018-06-08 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29884837 Genome-wide association study identifies genes associated with neuropathy in patients with head and neck cancer. Neuropathic pain in head and neck cancer 130 European ancestry cases, 913 European ancestry controls NA Illumina [714494] 4 neuropathic pain http://www.ebi.ac.uk/efo/EFO_0005762 GCST005934 Genome-wide genotyping array 2018-07-20 29563502 Fejzo MS 2018-03-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29563502 Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum. Severity of nausea and vomiting of pregnancy 14,988 European ancestry individuals with no NVP, 14,292 European ancestry individuals with slight NVP, 17,786 European individuals with moderate NVP, 5,445 European ancestry individuals with severe NVP, 1,220 European ancestry individuals with very severe NVP NA Illumina [11956931] (imputed) 7 nausea and vomiting of pregnancy severity measurement http://www.ebi.ac.uk/efo/EFO_0009265 GCST005929 Genome-wide genotyping array 2018-07-20 29563502 Fejzo MS 2018-03-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29563502 Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum. Hyperemesis gravidarum 1,306 European ancestry cases, 15,756 European ancestry controls without nausea and vomiting of pregnancy (NVP) 899 European ancestry cases, 749 European ancestry controls with and without nausea and vomiting of pregnancy (NVP) Illumina [12687884] (imputed) 2 hyperemesis gravidarum http://www.ebi.ac.uk/efo/EFO_1000971 GCST005930 Genome-wide genotyping array 2019-08-16 31207883 Rivera-Paredez B 2019-06-14 Nutrients www.ncbi.nlm.nih.gov/pubmed/31207883 Influence of Genetic and Non-Genetic Risk Factors for Serum Uric Acid Levels and Hyperuricemia in Mexicans. Serum uric acid levels 396 Mexican ancestry individuals 3,693 Mexican ancestry individuals Illumina [7200000] (imputed) 3 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST008445 Genome-wide genotyping array 2019-10-24 31040135 Dahlin AM 2019-04-30 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/31040135 Genetic Variants in the 9p21.3 Locus Associated with Glioma Risk in Children, Adolescents, and Young Adults: a Case-control Study. Glioma (pediatric/youth onset) 854 European ancestry cases, 3,689 European ancestry controls NA Illumina [8831628] (imputed) 0 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST008912 Genome-wide genotyping array 2021-12-06 31049583 Hadji-Turdeghal K 2019-05-03 Cardiovasc Res www.ncbi.nlm.nih.gov/pubmed/31049583 Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse. ICD10 R55: Syncope and collapse 9,163 British ancestry cases, 399,798 British ancestry controls 2,352 European ancestry cases, 51,929 European ancestry controls NR [805426] 1 Syncope http://purl.obolibrary.org/obo/HP_0001279 GCST012579 Genome-wide genotyping array 2019-06-17 25631608 Wessel J 2015-01-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25631608 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Fasting blood insulin 35,380 European ancestry non-diabetic individuals, 12,738 African American non-diabetic individuals NA Illumina [197481] 7 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST007898 Exome genotyping array [Exome array] 2019-06-17 25631608 Wessel J 2015-01-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25631608 Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility. Fasting blood glucose 50,900 European ancestry non-diabetic individuals, 9,664 African American non-diabetic individuals NA Illumina [197481] 22 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST007899 Exome genotyping array [Exome array] 2018-06-06 29674289 Cheon EJ 2018-04-12 Atherosclerosis www.ncbi.nlm.nih.gov/pubmed/29674289 Novel association between CDKAL1 and cholesterol efflux capacity: Replication after GWAS-based discovery. Cholesterol efflux capacity 607 East Asian ancestry individuals 158 East Asian ancestry individuals Affymetrix [~ 5800000] (imputed) 3 cholesterol efflux capacity measurement http://www.ebi.ac.uk/efo/EFO_0009132 GCST005671 Genome-wide genotyping array 2018-12-17 29483656 Pardinas AF 2018-02-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29483656 Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. Schizophrenia 40,675 European ancestry cases, 64,643 European ancestry controls 1,651 European ancestry cases, 4,111 cases, 142,717 European ancestry controls, 11,507 controls Illumina [8000000] (imputed) 108 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST006803 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Age of smoking initiation up to 341,427 European ancestry individuals NA NR [~ 10000000] (imputed) 10 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST007458 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Smoking behaviour (cigarettes smoked per day) up to 377,334 European ancestry individuals NA NR [~ 10000000] (imputed) 55 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST007459 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Smoking cessation up to 547,219 European ancestry individuals NA NR [~ 10000000] (imputed) 24 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST007460 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Smoking initiation (ever regular vs never regular) up to 1,232,091 European ancestry individuals NA NR [~ 10000000] (imputed) 378 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST007474 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Alcohol consumption (drinks per week) up to 941,280 European ancestry individuals NA NR [~ 10000000] (imputed) 99 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST007461 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Age of smoking initiation (MTAG) up to 931,815 European ancestry individuals NA NR [9732723] (imputed) 173 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST007462 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Cigarettes smoked per day (MTAG) up to 403,928 European ancestry individuals NA NR [9732723] (imputed) 88 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST007463 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Smoking cessation (MTAG) up to 820,192 European ancestry individuals NA NR [9732723] (imputed) 82 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST007464 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Smoking initiation (ever regular vs never regular) (MTAG) up to 1,359,002 European ancestry individuals NA NR [9732723] (imputed) 685 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST007468 Genome-wide genotyping array 2019-03-28 30643251 Liu M 2019-01-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30643251 Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use. Alcohol consumption (drinks per week) (MTAG) up to 1,039,210 European ancestry individuals NA NR [~ 9732723] (imputed) 155 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST007472 Genome-wide genotyping array 2019-09-16 31021400 Masotti M 2019-04-25 Biometrics www.ncbi.nlm.nih.gov/pubmed/31021400 Pleiotropy informed adaptive association test of multiple traits using GWAS summary data. Glycemic traits (pleiotropy) 46,186 European ancestry individuals NA NR [NR] 16 fasting blood glucose measurement, HOMA-B, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004465, http://www.ebi.ac.uk/efo/EFO_0004469, http://www.ebi.ac.uk/efo/EFO_0004466 GCST008674 Genome-wide genotyping array 2019-05-07 30368896 Niazi Y 2018-10-03 Environ Mol Mutagen www.ncbi.nlm.nih.gov/pubmed/30368896 Genetic variation associated with chromosomal aberration frequency: A genome-wide association study. Chromosomal aberration frequency (total) 576 European ancestry individuals 1,770 European ancestry individuals Illumina [10258281] (imputed) 0 chromosomal aberration frequency http://www.ebi.ac.uk/efo/EFO_0009860 GCST007722 Genome-wide genotyping array 2019-05-07 30368896 Niazi Y 2018-10-03 Environ Mol Mutagen www.ncbi.nlm.nih.gov/pubmed/30368896 Genetic variation associated with chromosomal aberration frequency: A genome-wide association study. Chromosomal aberration frequency (chromatid type) 576 European ancestry individuals 1,770 European ancestry individuals Illumina [10258281] (imputed) 0 chromatid-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009862 GCST007723 Genome-wide genotyping array 2019-05-07 30368896 Niazi Y 2018-10-03 Environ Mol Mutagen www.ncbi.nlm.nih.gov/pubmed/30368896 Genetic variation associated with chromosomal aberration frequency: A genome-wide association study. Chromosomal aberration frequency (chromosome type) 576 European ancestry individuals 1,770 European ancestry individuals Illumina [10258281] (imputed) 0 chromosome-type aberration frequency http://www.ebi.ac.uk/efo/EFO_0009861 GCST007724 Genome-wide genotyping array 2019-06-27 31036433 Pividori M 2019-04-26 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31036433 Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. Asthma (adult onset) 21,564 British ancestry cases, 318,237 British ancestry controls NA Affymetrix [10894596] (imputed) 28 adult onset asthma http://www.ebi.ac.uk/efo/EFO_1002011 GCST007993 Genome-wide genotyping array 2019-06-27 31036433 Pividori M 2019-04-26 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31036433 Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. Asthma (childhood onset) 9,433 British ancestry cases, 318,237 British ancestry controls NA Affymetrix [10894596] (imputed) 64 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST007995 Genome-wide genotyping array 2019-06-27 31036433 Pividori M 2019-04-26 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31036433 Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. Asthma (age of onset) 37,846 British ancestry individuals NA Affymetrix [10894596] (imputed) 31 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007994 Genome-wide genotyping array 2019-06-27 31036433 Pividori M 2019-04-26 Lancet Respir Med www.ncbi.nlm.nih.gov/pubmed/31036433 Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies. Chronic obstructive pulmonary disease 9,876 British ancestry cases, 318,237 British ancestry controls NA Affymetrix [10894596] (imputed) 1 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST007996 Genome-wide genotyping array 2019-07-12 31049640 Chen J 2019-05-02 Diabetologia www.ncbi.nlm.nih.gov/pubmed/31049640 Genome-wide association study of type 2 diabetes in Africa. Type 2 diabetes 2,633 African ancestry cases, 1,714 African ancestry controls NA Affymetrix, Illumina [12148595] (imputed) 40 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST008114 Genome-wide genotyping array 2019-10-23 31564434 Wells HRR 2019-09-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31564434 GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank. Adult hearing difficulty 87,056 British ancestry cases, 163,333 British ancestry controls 30,765 European ancestry individuals Affymetrix [9740198] (imputed) 3 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST008899 Genome-wide genotyping array 2019-10-23 31564434 Wells HRR 2019-09-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31564434 GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank. Adult hearing aid use 13,178 British ancestry cases, 240,740 British ancestry controls 35,004 European ancestry individuals Affymetrix [9740198] (imputed) 1 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST008898 Genome-wide genotyping array 2019-04-09 30767168 Shin JH 2019-02-14 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/30767168 Genetic risk score combining six genetic variants associated with the cellular NRF2 expression levels correlates with Type 2 diabetes in the human population. Cellular nuclear factor (erythroid-derived 2)-like 2 levels 74 East Asian ancestry lymphoblastoid cell lines NA Affymetrix [352228] (imputed) 6 NRF2 measurement http://www.ebi.ac.uk/efo/EFO_0009794 GCST007538 Genome-wide genotyping array 2020-07-21 32277175 Han X 2020-04-10 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/32277175 Genome-wide meta-analysis identifies novel loci associated with age-related macular degeneration. Age-related macular degeneration (MTAG) 37,342 European ancestry cases, 92,890 European ancestry controls 7,126 European ancestry cases, 174,286 European ancestry controls NR [NR] (imputed) 4 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST010284 Genome-wide genotyping array 2020-02-27 31888951 Schlauch KA 2019-12-30 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31888951 A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort. Body mass index 5,994 non-diabetic individuals, 651 diabetic individuals NA Illumina [500508] 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009701 Genome-wide genotyping array 2020-02-27 31888951 Schlauch KA 2019-12-30 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31888951 A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort. Obesity (extreme) 984 cases, 2,012 controls NA Illumina [500508] 9 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST009700 Genome-wide genotyping array 2020-02-27 31888951 Schlauch KA 2019-12-30 G3 (Bethesda) www.ncbi.nlm.nih.gov/pubmed/31888951 A Comprehensive Genome-Wide and Phenome-Wide Examination of BMI and Obesity in a Northern Nevadan Cohort. Body mass index 5,994 non-diabetic individuals NA Illumina [500508] 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009702 Genome-wide genotyping array 2019-08-15 31243853 Chung S 2019-06-27 J Viral Hepat www.ncbi.nlm.nih.gov/pubmed/31243853 GWAS identifying HLA-DPB1 gene variants associated with responsiveness to hepatitis B virus vaccination in Koreans: Independent association of HLA-DPB1*04:02 possessing rs1042169 G - rs9277355 C - rs9277356 A. Response to hepatitis B vaccine 1,760 Korean ancestry non-responder adults, 5,107 Korean ancestry responder adults 2,327 Korean ancestry adults, 49 Korean ancestry non-responder infants, 234 Korean ancestry responder infants Affymetrix [345072] 1 Anti-hepatitis B virus surface antigen IgG measurement, response to vaccine http://www.ebi.ac.uk/efo/EFO_0009358, http://www.ebi.ac.uk/efo/EFO_0004645 GCST008435 Genome-wide genotyping array 2021-03-30 32778093 He B 2020-08-10 BMC Biol www.ncbi.nlm.nih.gov/pubmed/32778093 Genome-wide pQTL analysis of protein expression regulatory networks in the human liver. Protein quantitative trait loci (liver) 172 European ancestry individuals, 29 Black individuals, 86 individuals NA Illumina [1671387] (imputed) 2897 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST011427 Genome-wide genotyping array 2019-05-08 30382898 Moon S 2018-11-01 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/30382898 Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population. Metabolic syndrome 1,328 Korean ancestry cases, 5,870 Korean ancestry controls 309 Korean ancestry cases, 2,529 Korean ancestry controls Affymetrix [351983] 24 metabolic syndrome http://www.ebi.ac.uk/efo/EFO_0000195 GCST007738 Genome-wide genotyping array 2019-04-11 30353303 Seo M 2018-10-23 J Mol Med (Berl) www.ncbi.nlm.nih.gov/pubmed/30353303 Genomics and response to long-term oxygen therapy in chronic obstructive pulmonary disease. Response to long-term oxygen therapy in chronic obstructive pulmonary disease 290 European ancestry individuals NA Illumina [5946283] (imputed) 14 response to supplemental oxygen http://www.ebi.ac.uk/efo/EFO_0009796 GCST007558 Genome-wide genotyping array 2019-10-24 31009096 Meda SA 2019-04-22 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/31009096 Multivariate analyses reveal biological components related to neuronal signaling and immunity mediating EEG abnormalities in alcohol-dependent individuals from the COGA cohort. Alcohol use disorder 432 European American cases, 367 European American controls NA Illumina [473846] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST008911 Genome-wide genotyping array 2019-05-23 24507774 Peloso GM 2014-02-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24507774 Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. HDL cholesterol up to 42,208 European ancestry individuals, up to 14,330 African ancestry individuals NA Illumina [247644] 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007850 Targeted genotyping array [Exome array] 2019-05-23 24507774 Peloso GM 2014-02-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24507774 Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. LDL cholesterol up to 42,208 European ancestry individuals, up to 14,330 African ancestry individuals NA Illumina [247644] 5 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST007848 Targeted genotyping array [Exome array] 2019-05-23 24507774 Peloso GM 2014-02-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/24507774 Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks. Triglycerides up to 42,208 European ancestry individuals, up to 14,330 African ancestry individuals NA Illumina [247644] 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST007849 Targeted genotyping array [Exome array] 2019-06-27 31089142 Law PJ 2019-05-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31089142 Association analyses identify 31 new risk loci for colorectal cancer susceptibility. Colorectal cancer 31,197 European ancestry cases, 61,770 European ancestry controls NA Affymetrix, Illumina [> 10000000] (imputed) 87 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST007992 Genome-wide genotyping array 2018-08-01 29698419 Pande M 2018-04-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/29698419 Genetic susceptibility markers for a breast-colorectal cancer phenotype: Exploratory results from genome-wide association studies. Breast cancer and/or colorectal cancer 589 European ancestry colorectal cancer with a family history of breast cancer cases, 378 European ancestry breast cancer cases with a family history of colorectal cancer cases, 18 European ancestry breast and colorectal cancer cases, 1,769 European ancestry controls NA Illumina [6220060] (imputed) 18 colorectal cancer, breast carcinoma http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0000305 GCST006035 Genome-wide genotyping array 2019-06-03 31085060 Gisbert L 2019-05-10 Eur Neuropsychopharmacol www.ncbi.nlm.nih.gov/pubmed/31085060 Genome-wide analysis of emotional lability in adult attention deficit hyperactivity disorder (ADHD). Emotional lability in attention deficit hyperactivity disorder 563 European ancestry individuals NA Illumina [2777520] (imputed) 8 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST007880 Genome-wide genotyping array 2019-08-01 31014085 Welsh P 2019-04-24 Circulation www.ncbi.nlm.nih.gov/pubmed/31014085 Cardiac Troponin T and Troponin I in the General Population: Comparing and Contrasting their Genetic Determinants and Associations with Outcomes. Cardiac Troponin-T levels 10,395 European ancestry individuals NA Illumina [24111857] (imputed) 13 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST008310 Genome-wide genotyping array 2019-08-01 31014085 Welsh P 2019-04-24 Circulation www.ncbi.nlm.nih.gov/pubmed/31014085 Cardiac Troponin T and Troponin I in the General Population: Comparing and Contrasting their Genetic Determinants and Associations with Outcomes. Cardiac troponin-I levels 14,579 European ancestry individuals NA Illumina [24111857] (imputed) 14 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST008309 Genome-wide genotyping array 2020-03-10 31879220 Lin GW 2019-12-23 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/31879220 Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study in multiple populations. Extranodal natural killer T-cell lymphoma (nasal type) 700 Han Chinese ancestry cases, 7,752 Han Chinese ancestry controls 717 East Asian ancestry cases, 12,650 East Asian ancestry controls Illumina [3892410] (imputed) 2 extranodal nasal NK/T cell lymphoma http://purl.obolibrary.org/obo/MONDO_0019472 GCST009759 Genome-wide genotyping array 2020-10-08 27470079 Li Z 2016-07-25 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/27470079 Genetic risk of extranodal natural killer T-cell lymphoma: a genome-wide association study. Extranodal natural killer T-cell lymphoma (nasal type) 189 East Asian ancestry cases, 957 East Asian ancestry controls 514 East Asian ancestry cases, 5,822 East Asian ancestry controls Illumina [477644] (imputed) 1 extranodal nasal NK/T cell lymphoma http://purl.obolibrary.org/obo/MONDO_0019472 GCST010657 Genome-wide genotyping array 2020-07-23 32277301 Okuda H 2020-04-10 Clin Exp Nephrol www.ncbi.nlm.nih.gov/pubmed/32277301 Genome-wide association study identifies new loci for albuminuria in the Japanese population. Urinary albumin excretion 7,805 Japanese ancestry individuals NA Illumina [4962728] (imputed) 15 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST010307 Genome-wide genotyping array 2021-06-25 33341150 Jabbari E 2020-12-17 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/33341150 Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study. Survival in progressive supranuclear palsy 1,001 European ancestry individuals 415 European ancestry individuals Illumina [4817946] (imputed) 1 overall survival, progressive supranuclear palsy http://www.ebi.ac.uk/efo/EFO_0000638, http://purl.obolibrary.org/obo/MONDO_0019037 GCST011977 Genome-wide genotyping array 2021-03-22 33345186 Li S 2020-10-28 Brain Commun www.ncbi.nlm.nih.gov/pubmed/33345186 The genetics of circulating BDNF: towards understanding the role of BDNF in brain structure and function in middle and old ages. Brain-derived neurotrophic factor levels 11,785 European ancestry individuals NA Affymetrix, Illumina [9950208] (imputed) 7 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST011378 Genome-wide genotyping array 2019-04-18 30388399 Ligthart S 2018-11-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30388399 Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. C-reactive protein levels up to 92,771 European ancestry males, up to 113,387 European ancestry females NA Affymetrix, Illumina, Perlegen [2437193] (imputed) 56 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST007614 Genome-wide genotyping array 2019-04-18 30388399 Ligthart S 2018-11-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30388399 Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. C-reactive protein levels 148,164 European ancestry individuals NA Affymetrix, Illumina, Perlegen [10019203] (imputed) 80 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST007615 Genome-wide genotyping array 2019-07-25 31231134 Laskar RS 2019-06-23 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31231134 Sex specific associations in genome wide association analysis of renal cell carcinoma. Renal cell carcinoma 1,992 European ancestry female cases, 3,095 European ancestry female controls 1,399 European ancestry female cases, 1,575 European ancestry female controls Illumina [~ 6000000] (imputed) 3 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST008225 Genome-wide genotyping array 2019-07-25 31231134 Laskar RS 2019-06-23 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31231134 Sex specific associations in genome wide association analysis of renal cell carcinoma. Renal cell carcinoma x sex interaction 3,227 European ancestry male cases, 1,992 European ancestry female cases, 4,916 European ancestry male controls, 3,095 European ancestry female controls 2,261 European ancestry male cases, 5,852 European ancestry male controls, 1,399 European ancestry female cases, 1,575 European ancestry female controls Illumina [~ 6000000] (imputed) 1 sex interaction measurement, renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0000681 GCST008224 Genome-wide genotyping array 2019-07-25 31231134 Laskar RS 2019-06-23 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/31231134 Sex specific associations in genome wide association analysis of renal cell carcinoma. Renal cell carcinoma 3,227 European ancestry male cases, 4,916 European ancestry male controls 2,261 European ancestry male cases, 5,852 European ancestry male controls Illumina [~ 6000000] (imputed) 8 renal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000681 GCST008226 Genome-wide genotyping array 2019-08-01 31000673 Kim W 2019-04-18 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/31000673 A Genome-Wide Association Study implicates NR2F2 in Lymphangioleiomyomatosis Pathogenesis. Lymphangioleiomyomatosis (sporadic) 426 European ancestry cases, 852 European ancestry controls 196 European ancestry cases, up to 226,140 European ancestry controls, up to 1,121 Hispanic white controls Illumina [5426936] (imputed) 1 lymphangioleiomyomatosis http://purl.obolibrary.org/obo/MONDO_0011705 GCST008311 Genome-wide genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence 2,411 European ancestry cases, 880 African American cases, 2,438 European ancestry controls, 951 African American controls 2,280 European ancestry cases, 1,911 African American cases, 1,964 European ancestry controls, 815 African American controls Illumina [up to 8021023] (imputed) 1 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST008284 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence symptom count 7,418 European ancestry individuals, 3,175 African American individuals 5,053 European ancestry individuals, 2,940 African American individuals Illumina [up to 8021023] (imputed) 1 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST008283 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence (tolerance) 3,348 European ancestry cases, 1,110 African American cases, 3,958 European ancestry controls, 2,024 African American controls 3,051 European ancestry cases, 1,545 African American cases, 2,001 European ancestry controls, 1,395 African American controls Illumina [up to 8021023] (imputed) 1 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST008285 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence (withdrawal) 1,259 European ancestry cases, 514 African American cases, 6,046 European ancestry controls, 2,616 African American controls 735 European ancestry cases, 894 African American cases, 4,318 European ancestry controls, 2,046 African American controls Illumina [up to 8021023] (imputed) 0 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST008286 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence (drinking more than intended) 3,826 European ancestry cases, 1,317 African American cases, 3,480 European ancestry controls, 1,817 African American controls 3,129 European ancestry cases, 2,032 African American cases, 1,921 European ancestry controls, 906 African American controls Illumina [up to 8021023] (imputed) 1 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST008287 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence (desire to cut drinking) 2,896 European ancestry cases, 1,436 African American cases, 4,413 European ancestry controls, 1,701 African American controls 2,021 European ancestry cases, 1,836 African American cases, 3,032 European ancestry controls, 1,104 African American controls Illumina [up to 8021023] (imputed) 1 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST008288 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence (giving up activities) 1,437 European ancestry cases, 578 African American cases, 5,871 European ancestry controls, 2,558 African American controls 520 European ancestry cases, 1,416 African American cases, 4,533 European ancestry controls, 1,524 African American controls Illumina [up to 8021023] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST008289 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence (time spent drinking) 1,533 European ancestry cases, 546 African American cases, 5,776 European ancestry controls, 2,590 African American controls 1,022 European ancestry cases, 1,255 African American cases, 4,031 European ancestry controls, 1,685 African American controls Illumina [up to 8021023] (imputed) 1 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST008290 Genome-wide genotyping array, Targeted genotyping array 2019-08-01 31090166 Lai D 2019-05-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31090166 Genome-wide association studies of alcohol dependence, DSM-IV criterion count, and individual criteria. Alcohol dependence (drinking despite problems) 2,163 European ancestry cases, 784 African American cases, 5,144 European ancestry controls, 2,351 African American controls 1,921 European ancestry cases, 1,299 African American cases, 3,131 European ancestry controls, 1,640 African American controls Illumina [up to 8021023] (imputed) 0 alcohol dependence measurement http://www.ebi.ac.uk/efo/EFO_0007835 GCST008291 Genome-wide genotyping array, Targeted genotyping array 2018-11-09 29673008 Bonfiglio F 2018-04-19 Neurogastroenterol Motil www.ncbi.nlm.nih.gov/pubmed/29673008 A GWAS meta-analysis from 5 population-based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome. Irritable bowel syndrome 1,335 European ancestry cases, 9,768 European ancestry controls NA Illumina [2483385] (imputed) 7 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST006535 Genome-wide genotyping array 2019-06-21 31092297 Guan M 2019-05-15 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/31092297 Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans. Type 2 diabetes and end-stage kidney disease 3,432 African-American cases, 6,977 African-American controls NA Affymetrix, Illumina [NR] (imputed) 25 diabetic nephropathy, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000401, http://purl.obolibrary.org/obo/MONDO_0005148 GCST007949 Genome-wide genotyping array 2019-06-21 31092297 Guan M 2019-05-15 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/31092297 Genome-wide association study identifies novel loci for type 2 diabetes-attributed end-stage kidney disease in African Americans. Type 2 diabetes and end-stage kidney disease in APOL1 risk genotype negative individuals 2,768 African-American cases, 6,059 African-American controls NA Affymetrix, Illumina [NR] (imputed) 13 diabetic nephropathy, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000401, http://purl.obolibrary.org/obo/MONDO_0005148 GCST007950 Genome-wide genotyping array 2018-08-13 29844195 Hosoda Y 2018-05-29 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/29844195 CFH and VIPR2 as susceptibility loci in choroidal thickness and pachychoroid disease central serous chorioretinopathy. Sub-foveal choroidal thickness 3,418 Japanese ancestry individuals 2,692 Japanese ancestry individuals Illumina [4710779] (imputed) 2 choroidal thickness measurement http://www.ebi.ac.uk/efo/EFO_0009281 GCST006068 Genome-wide genotyping array, Targeted genotyping array 2020-12-15 32981178 Masuda T 2020-09-27 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/32981178 A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese. Ovarian cancer 647 Japanese ancestry cases, 39,556 Japanese ancestry controls NA NR [> 7000000] (imputed) 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST010880 Genome-wide genotyping array 2020-12-15 32981178 Masuda T 2020-09-27 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/32981178 A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese. Endometrial cancer 909 Japanese ancestry cases, 39,556 Japanese ancestry controls NA NR [> 7000000] (imputed) 0 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST010879 Genome-wide genotyping array 2020-12-15 32981178 Masuda T 2020-09-27 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/32981178 A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese. Cervical cancer 538 Japanese ancestry cases, 39,556 Japanese ancestry controls NA NR [> 7000000] (imputed) 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST010878 Genome-wide genotyping array 2020-12-15 32981178 Masuda T 2020-09-27 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/32981178 A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese. Endometriosis 645 Japanese ancestry cases, 39,556 Japanese ancestry controls NA NR [> 7000000] (imputed) 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST010877 Genome-wide genotyping array 2020-12-15 32981178 Masuda T 2020-09-27 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/32981178 A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese. Uterine fibroids 5,236 Japanese ancestry cases, 39,556 Japanese ancestry controls NA NR [> 7000000] (imputed) 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST010876 Genome-wide genotyping array 2020-12-15 32981178 Masuda T 2020-09-27 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/32981178 A Mendelian randomization study identified obesity as a causal risk factor of uterine endometrial cancer in Japanese. Body mass index 105,534 Japanese ancestry individuals NA NR [> 7000000] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST010881 Genome-wide genotyping array 2019-05-20 31070104 Jia Q 2019-05-09 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/31070104 Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease. Glycine levels 19,112 European ancestry male individuals NA Affymetrix, Illumina [7487927] (imputed) 10 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST007838 Genome-wide genotyping array 2019-05-20 31070104 Jia Q 2019-05-09 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/31070104 Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease. Glycine levels 11,006 European ancestry female individuals NA Affymetrix, Illumina [7487927] (imputed) 7 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST007837 Genome-wide genotyping array 2019-05-20 31070104 Jia Q 2019-05-09 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/31070104 Genetic Determinants of Circulating Glycine Levels and Risk of Coronary Artery Disease. Glycine levels 30,118 European ancestry individuals NA Affymetrix, Illumina [7487927] (imputed) 12 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST007836 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_17:1_[M+OAc]1-/Lysophosphatidylserine_21:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060174 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_17:2_[M+H]1+/Lysophosphatidylethanolamine_20:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060153 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_18:2_[M+OAc]1-/Lysophosphatidylserine_22:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060180 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_20:3_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060192 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_20:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 54 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060167 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_20:4_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060190 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine_22:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060175 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine-2O_16:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060146 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine-2O_16:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060166 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine-2O_18:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060158 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine-O_16:1_[M+H]1+/Lysophosphatidylcholine-P_16:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060144 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine-O_18:2_[M+H]1+/Lysophosphatidylcholine-P_18:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060155 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(15:0)_[M+H]1+/Lysophosphatidylethanolamine(18:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060592 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(16:0)_[M+H]1+/Lysophosphatidylethanolamine(19:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060594 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(16:1)_[M+H]1+/Lysophosphatidylethanolamine(19:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060593 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(17:0)_[M+H]1+/Lysophosphatidylethanolamine(20:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060595 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(18:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060600 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(18:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060598 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(18:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060596 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylcholine(20:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 68 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90060602 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_16:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 13 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060137 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_18:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060143 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_18:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060141 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_18:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 26 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060139 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_18:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060140 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_19:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060149 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_20:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060156 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_20:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060154 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_20:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060152 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_20:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 40 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060151 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_22:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 52 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060164 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine_22:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060162 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine-O_16:1_[M-H]1-/Lysophosphatidylethanolamine-P_16:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060136 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine-O_18:1_[M-H]1-/Lysophosphatidylethanolamine-P_18:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060138 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine-P_19:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060142 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylethanolamine-P_20:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90060147 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Lysophosphatidylserine_20:0_[M+H]1+/Lysohosphatidylglycerols_20:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 lysophosphatidylserine measurement http://www.ebi.ac.uk/efo/EFO_0020048 GCST90060170 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C12H18O3)_jasmonic acid_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060093 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C12H18O4)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060096 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C12H20O3)_dihydrojasmonic_acid_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060094 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C13H20O3)_methyl_jasmonate_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060095 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C18H26O3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060109 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C18H30O3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060110 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C18H30O4)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060119 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C18H32O4)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060121 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Octadecanoid(C18H34O5)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 octadecanoids measurement http://www.ebi.ac.uk/efo/EFO_0020043 GCST90060126 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Oxocholesterol_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060134 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate_34:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 12 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060223 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate_36:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060233 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(34:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060687 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(32:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 59 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060633 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(32:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 336 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060641 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(32:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060683 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(32:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060678 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(33:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060708 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(33:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060640 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(33:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060705 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:0)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 15 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060647 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 31 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060657 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060732 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 6 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060644 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 30 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060655 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060727 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:2)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060643 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 20 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060652 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(34:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060721 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(35:2)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060751 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:0)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 16 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060668 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:0)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 28 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060685 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:0)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060789 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:1)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 16 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060664 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 28 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060680 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060782 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:2)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060662 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(36:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 19 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060673 Genome-wide genotyping array 2022-01-11 34620984 Skuladottir AT 2021-10-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34620984 A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo. Vertigo 48,072 European ancestry cases, 894,541 European ancestry controls NA Affymetrix, Illumina [62056310] (imputed) 100 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90085927 Genome-wide genotyping array, Genome-wide sequencing 2021-11-03 34521259 Sundbaum JK 2021-09-15 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/34521259 Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate. Alanine aminotransferase level after methotrexate initiation in rheumatoid arthritis 194 individuals 160 individuals Illumina [7585873] (imputed) 1 response to methotrexate, serum alanine aminotransferase measurement http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004735 GCST90044897 Genome-wide genotyping array 2021-11-03 34521259 Sundbaum JK 2021-09-15 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/34521259 Genome-wide association study of liver enzyme elevation in rheumatoid arthritis patients starting methotrexate. Alanine aminotransferase elevation after methotrexate initiation in rheumatoid arthritis (>1.5 × ULN) 18 cases, 180 controls NA Illumina [7585873] (imputed) 0 response to methotrexate, serum alanine aminotransferase measurement http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004735 GCST90061439 Genome-wide genotyping array 2021-08-13 34099642 de Rojas I 2021-06-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34099642 Common variants in Alzheimer's disease and risk stratification by polygenic risk scores. Alzheimer's disease 36,675 European ancestry cases, up to 42,034 European ancestry maternal or paternal cases, up to 372,760 European ancestry controls 19,087 European ancestry cases, 39,101 European ancestry controls Affymetrix, Illumina [up to 14542816] (imputed) 14 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST012182 Genome-wide genotyping array 2021-10-19 34616010 Quintanilha JCF 2021-10-06 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/34616010 Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients. Bevacizumab-induced hypertension 1,039 European ancestry individuals NA Illumina [833710] 2 response to bevacizumab, hypertension http://www.ebi.ac.uk/efo/EFO_0005943, http://www.ebi.ac.uk/efo/EFO_0000537 GCST90026609 Genome-wide genotyping array 2021-10-20 34616010 Quintanilha JCF 2021-10-06 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/34616010 Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients. Bevacizumab-induced proteinuria 1,039 European ancestry individuals NA Illumina [828141] 4 response to bevacizumab, Proteinuria http://www.ebi.ac.uk/efo/EFO_0005943, http://purl.obolibrary.org/obo/HP_0000093 GCST90026610 Genome-wide genotyping array 2021-10-20 34616010 Quintanilha JCF 2021-10-06 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/34616010 Bevacizumab-induced hypertension and proteinuria: a genome-wide study of more than 1000 patients. Bevacizumab-induced composite toxicity (either hypertension or proteinuria) 1,039 European ancestry individuals NA Illumina [828141] 6 response to bevacizumab, hypertension, Proteinuria http://www.ebi.ac.uk/efo/EFO_0005943, http://www.ebi.ac.uk/efo/EFO_0000537, http://purl.obolibrary.org/obo/HP_0000093 GCST90026611 Genome-wide genotyping array 2021-10-06 34108613 Ivarsdottir EV 2021-06-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34108613 The genetic architecture of age-related hearing impairment revealed by genome-wide association analysis. Age-related hearing impairment 121,934 European ancestry cases, 591,699 European ancestry controls NA Affymetrix, Illumina [46900000] (imputed) 51 age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0005782 GCST012442 Genome-wide genotyping array, Genome-wide sequencing, Exome-wide sequencing 2022-03-04 34353775 Galesloot TE 2021-08-02 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/34353775 Genome-wide Meta-analysis Identifies Novel Genes Associated with Recurrence and Progression in Non-muscle-invasive Bladder Cancer. Recurrence-free survival in non-muscle-invasive bladder cancer 3,400 European ancestry individuals NA Illumina [7591411] (imputed) 13 event free survival time, urinary bladder cancer http://www.ebi.ac.uk/efo/EFO_0000482, http://purl.obolibrary.org/obo/MONDO_0001187 GCST90095079 Genome-wide genotyping array 2022-03-04 34353775 Galesloot TE 2021-08-02 Eur Urol Oncol www.ncbi.nlm.nih.gov/pubmed/34353775 Genome-wide Meta-analysis Identifies Novel Genes Associated with Recurrence and Progression in Non-muscle-invasive Bladder Cancer. Progression-free survival in non-muscle-invasive bladder cancer 3,400 European ancestry individuals NA Illumina [7582931] (imputed) 8 progression free survival, urinary bladder cancer http://www.ebi.ac.uk/efo/EFO_0004920, http://purl.obolibrary.org/obo/MONDO_0001187 GCST90095080 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android fat mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90026418 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid fat mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90026419 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm fat mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90026420 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg fat mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90026421 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk fat mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90026422 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Visceral adipose tissue mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90026423 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Visceral adipose tissue volume 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90026424 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android lean mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026425 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid lean mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026426 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm lean mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026427 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg lean mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026428 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk lean mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026429 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android bone mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST90026430 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid bone mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST90026431 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm bone mineral content 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90026432 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg bone mineral content 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90026433 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk bone mineral content 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90026434 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (arm fat ratio) 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90026435 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (leg fat ratio) 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90026436 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (trunk fat ratio) 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90026437 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android fat/gynoid fat ratio 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90026438 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk fat/peripheral fat ratio 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90026439 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android total mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026440 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid total mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026441 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm total mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026442 Genome-wide genotyping array 2022-03-14 34237774 COVID-19 Host Genetics Initiative 2021-07-08 Nature www.ncbi.nlm.nih.gov/pubmed/34237774 Mapping the human genetic architecture of COVID-19. COVID-19 (critical illness vs population) 133 African ancestry cases, 2,610 African ancestry controls, 304 East Asian ancestry cases, 2,450 East Asian ancestry controls, 5,101 European ancestry cases, 1,383,241 European ancestry controls, 641 Hispanic or Latin American cases, 95,479 Hispanic or Latin American controls NA Illumina [NR] (imputed) 7 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90095123 Genome-wide genotyping array 2022-03-14 34237774 COVID-19 Host Genetics Initiative 2021-07-08 Nature www.ncbi.nlm.nih.gov/pubmed/34237774 Mapping the human genetic architecture of COVID-19. COVID-19 (hospitalized vs population) 790 African ancestry cases, 20,582 African ancestry controls, 60 Middle Eastern ancestry cases, 13,360 Middle Eastern ancestry controls, 1,414 East Asian ancestry cases, 15,499 East Asian ancestry controls, 9,986 European ancestry cases, 1,877,672 European ancestry controls, 186 South Asian ancestry cases, 43,280 South Asian ancestry controls, 1,678 Hispanic or Latin American cases, 100,316 Hispanic or Latin American controls NA Affymetrix, Illumina [NR] (imputed) 10 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90095124 Genome-wide genotyping array, Genome-wide sequencing 2022-03-14 34237774 COVID-19 Host Genetics Initiative 2021-07-08 Nature www.ncbi.nlm.nih.gov/pubmed/34237774 Mapping the human genetic architecture of COVID-19. SARS-CoV-2 infection 2,544 African ancestry cases, 31,176 African ancestry controls, 700 Middle Eastern ancestry cases, 13,360 Middle Eastern ancestry controls, 1,495 East Asian ancestry cases, 15,499 East Asian ancestry controls, 38,984 European ancestry cases, 1,644,784 European ancestry controls, 1,688 South Asian ancestry cases, 42,016 South Asian ancestry controls, 4,151 Hispanic or Latin American cases, 23,371 Hispanic or Latin American controls NA Affymetrix, Illumina, Perlegen [NR] (imputed) 9 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90095125 Genome-wide genotyping array, Genome-wide sequencing 2021-10-28 33133133 Lee KY 2020-08-28 Front Genet www.ncbi.nlm.nih.gov/pubmed/33133133 Genome-Wide Search for SNP Interactions in GWAS Data: Algorithm, Feasibility, Replication Using Schizophrenia Datasets. Schizophrenia (SNP x SNP interaction) 1,051 European ancestry cases, 1,214 European ancestry controls 829 African American or Afro-Caribbean cases, 874 African American or Afro-Caribbean controls, 1,176 European ancestry, African American or Afro-Caribbean cases, 1,325 European ancestry, African American or Afro-Caribbean controls NR [729454] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90058030 Genome-wide genotyping array 2021-06-07 33975060 Zhu Y 2021-05-07 Eur J Cancer www.ncbi.nlm.nih.gov/pubmed/33975060 A genetic variant conferred high expression of CAV2 promotes pancreatic cancer progression and associates with poor prognosis. Pancreatic ductal adenocarcinoma 518 Han Chinese ancestry cases 552 Han Chinese ancestry cases Illumina [Exome array] 1 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST011817 Exome genotyping array [Exome array] 2021-07-02 34038024 Kuo CL 2021-05-26 Aging Cell www.ncbi.nlm.nih.gov/pubmed/34038024 Genetic associations for two biological age measures point to distinct aging phenotypes. Biological age (BioAge) 98,446 European ancestry individuals 1,782 European ancestry individuals Affymetrix [16446666] (imputed) 0 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST011992 Genome-wide genotyping array 2021-07-02 34038024 Kuo CL 2021-05-26 Aging Cell www.ncbi.nlm.nih.gov/pubmed/34038024 Genetic associations for two biological age measures point to distinct aging phenotypes. Biological age (PhenoAge) 107,460 European ancestry individuals 5,572 European ancestry individuals Affymetrix [16446666] (imputed) 0 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST011993 Genome-wide genotyping array 2021-11-24 34246321 Fukunaga K 2021-07-10 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34246321 Genome-wide association study reveals an association between the HLA-DPB1∗02:01:02 allele and wheat-dependent exercise-induced anaphylaxis. Wheat-dependent exercise-induced anaphylaxis 77 Japanese ancestry cases, 924 Japanese ancestry controls 91 Japanese ancestry cases, 435 Japanese ancestry controls Illumina [3891096] (imputed) 5 wheat allergic reaction http://www.ebi.ac.uk/efo/EFO_1001243 GCST90026483 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer 9,241 African ancestry cases, 10,193 African ancestry controls, 122,977 European ancestry cases, 105,974 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 6 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90026461 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer (estrogen-receptor positive) 4,299 African ancestry cases, 10,193 African ancestry controls, 69,501 European ancestry cases, 105,974 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_1000649 GCST90026462 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer (estrogen-receptor negative) 2,636 African ancestry cases, 10,193 African ancestry controls, 21,468 European ancestry cases, 105,974 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 estrogen-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_1000650 GCST90026463 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer 9,241 African ancestry cases, 10,193 African ancestry controls NA Illumina [NR] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90026464 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer (estrogen-receptor positive) 4,299 African ancestry cases, 10,193 African ancestry controls NA Illumina [NR] (imputed) 0 estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_1000649 GCST90026465 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer (estrogen-receptor negative) 2,636 African ancestry cases, 10,193 African ancestry controls NA Illumina [NR] (imputed) 0 estrogen-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_1000650 GCST90026466 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer 122,977 European ancestry cases, 105,974 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 6 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90026467 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer (estrogen-receptor positive) 69,501 European ancestry cases, 105,974 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_1000649 GCST90026468 Genome-wide genotyping array 2021-11-19 34234117 Adedokun B 2021-07-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34234117 Cross-ancestry GWAS meta-analysis identifies six breast cancer loci in African and European ancestry women. Breast cancer (estrogen-receptor negative) 21,468 European ancestry cases, 105,974 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 2 estrogen-receptor negative breast cancer http://www.ebi.ac.uk/efo/EFO_1000650 GCST90026469 Genome-wide genotyping array 2021-06-08 34050153 Laabs BH 2021-05-28 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34050153 Identifying genetic modifiers of age-associated penetrance in X-linked dystonia-parkinsonism. X-linked dystonia-parkinsonism 353 Filipino ancestry individuals NA Illumina [4990999] (imputed) 0 X-linked dystonia-parkinsonism http://purl.obolibrary.org/obo/MONDO_0010747 GCST90014263 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Acute lymphoblastic leukemia 2,666 European ancestry cases, 60,272 European ancestry controls NA Affymetrix [8488517] (imputed) 0 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST90056175 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Lymphocyte count 234,778 European ancestry individuals 100,554 European ancestry individuals Affymetrix [10369434] (imputed) 196 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90085815 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Monocyte count 234,690 European ancestry individuals 100,494 European ancestry individuals Affymetrix [10369434] (imputed) 242 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90056177 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Neutrophil count 234,802 European ancestry individuals 100,556 European ancestry individuals Affymetrix [10369434] (imputed) 154 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90056178 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Basophil count 234,678 European ancestry individuals 100,513 European ancestry individuals Affymetrix [10369434] (imputed) 94 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90056179 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Eosinophil counts 234,763 European ancestry individuals 100,553 European ancestry individuals Affymetrix [10369434] (imputed) 189 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90056180 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Lymphocyte-to-monocyte ratio 234,184 European ancestry individuals 100,284 European ancestry individuals Affymetrix [10369434] (imputed) 218 lymphocyte:monocyte ratio http://www.ebi.ac.uk/efo/EFO_0600088 GCST90056181 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Neutrophil-to-lymphocyte ratio 234,502 European ancestry individuals 100,442 European ancestry individuals Affymetrix [10369434] (imputed) 108 neutrophil-to-lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0008447 GCST90056182 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Platelet count 235,256 European ancestry individuals 100,764 European ancestry individuals Affymetrix [10369434] (imputed) 359 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90056183 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Platelet-to-lymphocyte ratio 234,552 European ancestry individuals 100,478 European ancestry individuals Affymetrix [10369434] (imputed) 242 platelet-to-lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0008446 GCST90056184 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Lymphocyte-to-monocyte ratio 334,468 European ancestry, NR ancestry individuals NA Affymetrix [NR] (imputed) 104 lymphocyte:monocyte ratio http://www.ebi.ac.uk/efo/EFO_0600088 GCST90085816 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Neutrophil-to-lymphocyte ratio 334,944 European ancestry, NR ancestry individuals NA Affymetrix [NR] (imputed) 43 neutrophil-to-lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0008447 GCST90085817 Genome-wide genotyping array 2021-12-13 34469753 Kachuri L 2021-08-26 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34469753 Genetic determinants of blood-cell traits influence susceptibility to childhood acute lymphoblastic leukemia. Platelet-to-lymphocyte ratio 335,030 European ancestry, NR ancestry individuals NA Affymetrix [NR] (imputed) 92 platelet-to-lymphocyte ratio http://www.ebi.ac.uk/efo/EFO_0008446 GCST90085818 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Cranial base width 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90027862 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Upper facial depth 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90027863 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Middle facial depth 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90027864 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Lower facial depth 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90027865 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Morphological facial height 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90027866 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Upper facial height 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90027867 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Lower facial height 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90027868 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Intercanthal width 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90027869 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Outercanthal width 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90027870 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Palpebral fissure length 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 eye morphology measurement http://www.ebi.ac.uk/efo/EFO_0007858 GCST90027871 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Nasal width 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90027872 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Subnasal width 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90027873 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Nasal protrusion 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90027874 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Nasal ala length 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90027875 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Nasal height 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90027876 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Nasal bridge length 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90027877 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Labial fissure width 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007955 GCST90027878 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Philtrum length 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 mouth morphology measurement http://www.ebi.ac.uk/efo/EFO_0007955 GCST90027879 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Upper lip height 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 0 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90027880 Genome-wide genotyping array 2022-10-05 34434215 Liu D 2021-08-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/34434215 PRICKLE1 × FOCAD Interaction Revealed by Genome-Wide vQTL Analysis of Human Facial Traits. Lower lip height 2,447 European ancestry individuals 5,128 Korean ancestry individuals Illumina [3104639] (imputed) 1 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST90027881 Genome-wide genotyping array 2021-11-02 34475377 Reus LM 2021-09-02 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34475377 Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions. Frontotemporal dementia 354 Dutch ancestry cases, 4,209 Dutch ancestry controls 281 Dutch ancestry cases, 618 Dutch ancestry controls Illumina [39131578] (imputed) 2 frontotemporal dementia http://purl.obolibrary.org/obo/MONDO_0017276 GCST90038470 Genome-wide genotyping array 2022-01-07 34680877 Lybech LKM 2021-09-23 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34680877 Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings. Suicide related phenotype (previous attempted suicide) in bipolar disorder 25 Asian ancestry, Pacific Islander individuals, 53 Black ancestry, African American individuals, 5 Native American, Eskimo, Aleut individuals, 1,060 White ancestry individuals, 31 individuals NA Affymetrix [NR] (imputed) 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90085902 Genome-wide genotyping array 2022-01-07 34680877 Lybech LKM 2021-09-23 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34680877 Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings. Suicide related phenotype (fantasies about committing a violent suicide) in bipolar disorder 25 Asian ancestry, Pacific Islander individuals, 53 Black ancestry, African American individuals, 5 Native American, Eskimo, Aleut individuals, 1,060 White ancestry individuals, 31 individuals NA Affymetrix [NR] (imputed) 0 suicide ideation measurement http://www.ebi.ac.uk/efo/EFO_0007619 GCST90085903 Genome-wide genotyping array 2022-01-07 34680877 Lybech LKM 2021-09-23 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34680877 Suicide Related Phenotypes in a Bipolar Sample: Genetic Underpinnings. Suicide related phenotype (feeling that the life was not worth living) in bipolar disorder 25 Asian ancestry, Pacific Islander individuals, 53 Black ancestry, African American individuals, 5 Native American, Eskimo, Aleut individuals, 1,060 White ancestry individuals, 31 individuals NA Affymetrix [NR] (imputed) 1 suicide ideation measurement http://www.ebi.ac.uk/efo/EFO_0007619 GCST90085904 Genome-wide genotyping array 2021-10-14 34288885 Lin WD 2021-07-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/34288885 Genetic factors of idiopathic central precocious puberty and their polygenic risk in early puberty. Idiopathic central precocious puberty 256 Han Chinese ancestry cases, 118 Han Chinese ancestry controls 65 Han Chinese ancestry cases, 30 Han Chinese ancestry controls Affymetrix [NR] (imputed) 14 Central precocious puberty http://www.ebi.ac.uk/efo/EFO_0009029 GCST90027238 Genome-wide genotyping array 2021-06-21 34002480 Damotte V 2021-05-18 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/34002480 Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants. Plasma amyloid beta peptide concentrations (ABx-40) 12,369 European ancestry non-demented individuals NA Affymetrix, Illumina [NR] (imputed) 1 plasma beta-amyloid 1-40 measurement http://www.ebi.ac.uk/efo/EFO_0005659 GCST011942 Genome-wide genotyping array 2021-06-21 34002480 Damotte V 2021-05-18 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/34002480 Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants. Plasma amyloid beta peptide concentrations (ABx-42) 12,369 European ancestry non-demented individuals NA Affymetrix, Illumina [NR] (imputed) 1 plasma beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0005660 GCST011941 Genome-wide genotyping array 2021-06-21 34002480 Damotte V 2021-05-18 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/34002480 Plasma amyloid β levels are driven by genetic variants near APOE, BACE1, APP, PSEN2: A genome-wide association study in over 12,000 non-demented participants. Plasma amyloid beta peptide concentration (ABx-40/ABx-42 ratio) 12,369 European ancestry non-demented individuals NA Affymetrix, Illumina [NR] (imputed) 1 plasma beta-amyloid 1-40:1-42 ratio measurement http://www.ebi.ac.uk/efo/EFO_0600016 GCST011943 Genome-wide genotyping array 2021-09-23 34241624 Simpson CL 2021-07-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/34241624 Myopia in African Americans Is Significantly Linked to Chromosome 7p15.2-14.2. Myopia 295 African American cases, 100 African American controls, 132 African American individuals NA Illumina [98631] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST012379 Exome genotyping array [Exome array] 2021-10-06 34130359 Curtis SW 2021-06-15 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34130359 FAT4 identified as a potential modifier of orofacial cleft laterality. Unilateral cleft lip (left vs right) 68 Asian ancestry LCL cases, 78 European ancestry LCL cases, 70 Hispanic LCL cases, 43 Asian ancestry RCL cases, 40 European ancestry RCL cases, 47 Hispanic RCL cases 219 LCL cases, 107 RCL cases Illumina [539473] (imputed) 0 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST012453 Genome-wide genotyping array 2021-10-06 34130359 Curtis SW 2021-06-15 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34130359 FAT4 identified as a potential modifier of orofacial cleft laterality. Unilateral cleft lip and palate (left vs right) 98 Asian ancestry LCLP cases, 199 European ancestry LCLP cases, 340 Hispanic LCLP cases, 1 LCLP case, 59 Asian ancestry RCLP cases, 94 European ancestry RCLP cases, 263 Hispanic RCLP cases 428 LCLP cases, 250 RCLP cases Illumina [539473] (imputed) 0 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST012452 Genome-wide genotyping array 2021-10-06 34130359 Curtis SW 2021-06-15 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34130359 FAT4 identified as a potential modifier of orofacial cleft laterality. Right unilateral cleft lip 43 Asian ancestry cases, 40 European ancestry cases, 47 Hispanic cases, 1,626 controls NA Illumina [539473] (imputed) 21 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST012458 Genome-wide genotyping array 2021-10-06 34130359 Curtis SW 2021-06-15 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34130359 FAT4 identified as a potential modifier of orofacial cleft laterality. Left unilateral cleft lip and palate 98 Asian ancestry cases, 199 European ancestry cases, 340 Hispanic cases, 1 case, 1,626 controls NA Illumina [539473] (imputed) 22 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST012457 Genome-wide genotyping array 2021-10-06 34130359 Curtis SW 2021-06-15 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34130359 FAT4 identified as a potential modifier of orofacial cleft laterality. Left unilateral cleft lip 68 Asian ancestry cases, 78 European ancestry cases, 70 Hispanic cases, 1,626 controls NA Illumina [539473] (imputed) 32 cleft lip http://www.ebi.ac.uk/efo/EFO_0003959 GCST012456 Genome-wide genotyping array 2021-10-06 34130359 Curtis SW 2021-06-15 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34130359 FAT4 identified as a potential modifier of orofacial cleft laterality. Right unilateral cleft lip and palate 59 Asian ancestry cases, 94 European ancestry cases, 263 Hispanic cases, 1,626 controls NA Illumina [539473] (imputed) 22 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST012455 Genome-wide genotyping array 2021-10-06 34130359 Curtis SW 2021-06-15 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/34130359 FAT4 identified as a potential modifier of orofacial cleft laterality. Cleft lip with or without cleft palate (bilateral vs unilateral) 98 Asian ancestry LCLP cases, 199 European ancestry LCLP cases, 340 Hispanic LCLP cases, 1 LCLP case, 59 Asian ancestry RCLP cases, 94 European ancestry RCLP cases, 263 Hispanic RCLP cases, 68 Asian ancestry LCL cases, 78 European ancestry LCL cases, 70 Hispanic LCL cases, 43 Asian ancestry RCL cases, 40 European ancestry RCL cases, 47 Hispanic RCL cases 428 LCLP cases, 250 RCLP cases, 219 LCL cases, 107 RCL cases Illumina [539473] (imputed) 0 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST012454 Genome-wide genotyping array 2021-11-01 34469433 Ashvetiya T 2021-09-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/34469433 Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort. Abdominal aortic aneurysm 1,363 European, Indian, Caribbean, African ancestry cases, 27,260 European, Indian, Caribbean, African ancestry controls NA NR [NR] (imputed) 19 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST90038468 Genome-wide genotyping array 2021-11-01 34469433 Ashvetiya T 2021-09-01 PLoS One www.ncbi.nlm.nih.gov/pubmed/34469433 Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort. Thoracic aortic aneurysms 435 European, Indian, Caribbean, African ancestry cases, 8,700 European, Indian, Caribbean, African ancestry ancestry controls NA NR [NR] (imputed) 16 thoracic aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0004282 GCST90038469 Genome-wide genotyping array 2021-09-08 34431594 Atkins JL 2021-08-25 Aging Cell www.ncbi.nlm.nih.gov/pubmed/34431594 A genome-wide association study of the frailty index highlights brain pathways in ageing. Frailty index 175,226 European ancestry individuals NA Affymetrix, Illumina [7666890] (imputed) 14 frailty measurement http://www.ebi.ac.uk/efo/EFO_0009885 GCST90020053 Genome-wide genotyping array 2021-06-17 34067580 Kim HR 2021-05-17 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34067580 A Genome-Wide Association Study for Hypertensive Kidney Disease in Korean Men. Hypertensive renal disease 310 Korean ancestry male cases, 2,294 Korean ancestry male controls 43 Korean ancestry male cases, 636 Korean ancestry male controls Affymetrix [NR] (imputed) 4 hypertensive nephropathy http://purl.obolibrary.org/obo/MONDO_0024633 GCST011909 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Neuroticism conditioned on cognitive performance (multi-trait conditioning and joint analysis) 170,911 European ancestry individuals NA NR [NR] 93 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027239 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Neuroticism conditioned on Townsend deprivation index (multi-trait conditioning and joint analysis) 170,911 European ancestry individuals NA NR [NR] 100 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027240 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Neuroticism conditioned on educational attainment (multi-trait conditioning and joint analysis) 170,911 European ancestry individuals NA NR [NR] 81 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027241 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Neuroticism conditioned on highest math class (multi-trait conditioning and joint analysis) 170,911 European ancestry individuals NA NR [NR] 82 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027242 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Neuroticism conditioned on average household income before tax (multi-trait conditioning and joint analysis) 170,911 European ancestry individuals NA NR [NR] 59 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027243 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Neuroticism conditioned on self-rated math ability (multi-trait conditioning and joint analysis) 170,911 European ancestry individuals NA NR [NR] 70 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027244 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Subjective wellbeing conditioned on cognitive performance (multi-trait conditioning and joint analysis) 298,420 European ancestry individuals NA NR [NR] 2 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90032159 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Subjective wellbeing conditioned on Townsend deprivation index (multi-trait conditioning and joint analysis) 298,420 European ancestry individuals NA NR [NR] 3 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90032160 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Subjective wellbeing conditioned on educational attainment (multi-trait conditioning and joint analysis) 298,420 European ancestry individuals NA NR [NR] 2 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90032161 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Subjective wellbeing conditioned on highest math class (multi-trait conditioning and joint analysis) 298,420 European ancestry individuals NA NR [NR] 2 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90032162 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Subjective wellbeing conditioned on average household income before tax (multi-trait conditioning and joint analysis) 298,420 European ancestry individuals NA NR [NR] 3 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90032163 Genome-wide genotyping array 2021-09-24 33349686 Wendt FR 2020-12-21 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/33349686 Multivariate genome-wide analysis of education, socioeconomic status and brain phenome. Subjective wellbeing conditioned on self-rated math ability (multi-trait conditioning and joint analysis) 298,420 European ancestry individuals NA NR [NR] 2 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90032164 Genome-wide genotyping array 2021-08-24 34124712 Sherva R 2021-02-28 Explor Med www.ncbi.nlm.nih.gov/pubmed/34124712 Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Cocaine dependence (time to event) 3,554 African American cases, 478 African American controls, 2,712 European ancestry cases, 915 European ancestry controls 572 African American cases, 416 African American controls, 759 European ancestry cases, 1,620 European ancestry controls Illumina [NR] (imputed) 5 cocaine dependence http://www.ebi.ac.uk/efo/EFO_0002610 GCST012225 Genome-wide genotyping array 2021-08-24 34124712 Sherva R 2021-02-28 Explor Med www.ncbi.nlm.nih.gov/pubmed/34124712 Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Cocaine dependence (time to event) 3,554 African American cases, 478 African American controls 572 African American cases, 416 African American controls Illumina [NR] (imputed) 1 cocaine dependence http://www.ebi.ac.uk/efo/EFO_0002610 GCST012224 Genome-wide genotyping array 2021-08-24 34124712 Sherva R 2021-02-28 Explor Med www.ncbi.nlm.nih.gov/pubmed/34124712 Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Cocaine dependence (time to event) 2,712 European ancestry cases, 915 European ancestry controls 759 European ancestry cases, 1,620 European ancestry controls Illumina [NR] (imputed) 0 cocaine dependence http://www.ebi.ac.uk/efo/EFO_0002610 GCST012223 Genome-wide genotyping array 2021-08-24 34124712 Sherva R 2021-02-28 Explor Med www.ncbi.nlm.nih.gov/pubmed/34124712 Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Opioid dependence (time to event) 1,307 African American cases, 974 African American controls 144 African American cases, 354 African American controls Illumina [NR] (imputed) 7 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST012222 Genome-wide genotyping array 2021-08-24 34124712 Sherva R 2021-02-28 Explor Med www.ncbi.nlm.nih.gov/pubmed/34124712 Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Opioid dependence (time to event) 1,307 African American cases, 974 African American controls, 2,340 European ancestry cases, 768 European ancestry controls 144 African American cases, 354 African American controls, up to 1,551 European ancestry cases, up to 1,393 European ancestry controls Illumina [NR] (imputed) 3 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST012221 Genome-wide genotyping array 2021-08-24 34124712 Sherva R 2021-02-28 Explor Med www.ncbi.nlm.nih.gov/pubmed/34124712 Genome-wide association study of phenotypes measuring progression from first cocaine or opioid use to dependence reveals novel risk genes. Opioid dependence (time to event) 2,340 European ancestry cases, 768 European ancestry controls up to 1,551 European ancestry cases, up to 1,393 European ancestry controls Illumina [NR] (imputed) 0 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST012220 Genome-wide genotyping array 2022-03-09 34834492 Espuela-Ortiz A 2021-11-03 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834492 Role of Sex on the Genetic Susceptibility to Childhood Asthma in Latinos and African Americans. Childhood asthma x sex interaction 3,371 African ancestry, European ancestry, Native American ancestry cases, 2,650 African ancestry, European ancestry, Native American ancestry controls NA Affymetrix [6680224] (imputed) 4 childhood onset asthma, sex interaction measurement http://purl.obolibrary.org/obo/MONDO_0005405, http://www.ebi.ac.uk/efo/EFO_0008343 GCST90095141 Genome-wide genotyping array 2022-03-09 34834492 Espuela-Ortiz A 2021-11-03 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834492 Role of Sex on the Genetic Susceptibility to Childhood Asthma in Latinos and African Americans. Childhood asthma 3,075 African ancestry, European ancestry, Native American ancestry females NA Affymetrix [6680224] (imputed) 3 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90095142 Genome-wide genotyping array 2022-03-09 34834492 Espuela-Ortiz A 2021-11-03 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34834492 Role of Sex on the Genetic Susceptibility to Childhood Asthma in Latinos and African Americans. Childhood asthma 2,946 African ancestry, European ancestry, Native American ancestry individuals NA Affymetrix [6680224] (imputed) 0 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90095143 Genome-wide genotyping array 2021-11-02 34476894 Schmitz J 2021-09-03 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/34476894 Genome-wide association study and polygenic risk score analysis for hearing measures in children. Hearing function 5,344 European ancestry children NA Illumina [5305352] (imputed) 10 hearing threshold measurement http://www.ebi.ac.uk/efo/EFO_0007618 GCST90029040 Genome-wide genotyping array 2021-11-02 34476894 Schmitz J 2021-09-03 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/34476894 Genome-wide association study and polygenic risk score analysis for hearing measures in children. Hearing function (left/right asymmetry) 5,344 European ancestry children NA Illumina [5305352] (imputed) 9 hearing threshold measurement http://www.ebi.ac.uk/efo/EFO_0007618 GCST90029041 Genome-wide genotyping array 2021-11-02 34231218 McDonough CW 2021-07-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/34231218 Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS). Adverse cardiovascular outcome x beta blockers interaction in hypertension 9,195 European ancestry individuals NA Affymetrix, Illumina [6400000] (imputed) 10 response to beta blocker, cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0007766, http://www.ebi.ac.uk/efo/EFO_0006919 GCST90026457 Genome-wide genotyping array 2021-11-02 34231218 McDonough CW 2021-07-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/34231218 Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS). Adverse cardiovascular outcome x calcium channel blockers interaction in hypertension 10,511 European ancestry individuals NA Affymetrix, Illumina [6400000] (imputed) 3 response to calcium channel blocker, cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0007767, http://www.ebi.ac.uk/efo/EFO_0006919 GCST90026458 Genome-wide genotyping array 2021-11-02 34231218 McDonough CW 2021-07-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/34231218 Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS). Adverse cardiovascular outcome x ACE inhibitors/ARBs interaction in hypertension 2,559 European ancestry individuals NA Affymetrix, Illumina [6400000] (imputed) 3 response to angiotensin-converting enzyme inhibitor, cardiovascular event measurement, response to angiotensin receptor blocker http://www.ebi.ac.uk/efo/EFO_0005325, http://www.ebi.ac.uk/efo/EFO_0006919, http://www.ebi.ac.uk/efo/EFO_0010735 GCST90026459 Genome-wide genotyping array 2021-11-02 34231218 McDonough CW 2021-07-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/34231218 Adverse Cardiovascular Outcomes and Antihypertensive treatment: A Genome-Wide Interaction Meta-Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies (ICAPS). Adverse cardiovascular outcome x thiazide/thiazide-like diuretics interaction in hypertension 3,516 European ancestry individuals NA Affymetrix, Illumina [6400000] (imputed) 1 response to diuretic, cardiovascular event measurement http://purl.obolibrary.org/obo/GO_0036270, http://www.ebi.ac.uk/efo/EFO_0006919 GCST90026460 Genome-wide genotyping array 2021-08-25 33539531 Casares-Marfil D 2021-02-04 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/33539531 A genome-wide association study identifies novel susceptibility loci in chronic Chagas cardiomyopathy. Trypanosoma cruzi infection 1,019 Colombian ancestry cases, 1,104 Colombian ancestry controls NA Illumina [7846902] (imputed) 4 Trypanosoma cruzi seropositivity http://www.ebi.ac.uk/efo/EFO_0005530 GCST90026452 Genome-wide genotyping array 2021-08-25 33539531 Casares-Marfil D 2021-02-04 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/33539531 A genome-wide association study identifies novel susceptibility loci in chronic Chagas cardiomyopathy. Trypanosoma cruzi infection up to 213 Argentinian ancestry individuals NA Illumina [8408292] (imputed) 0 Trypanosoma cruzi seropositivity http://www.ebi.ac.uk/efo/EFO_0005530 GCST90026453 Genome-wide genotyping array 2021-08-25 33539531 Casares-Marfil D 2021-02-04 Clin Infect Dis www.ncbi.nlm.nih.gov/pubmed/33539531 A genome-wide association study identifies novel susceptibility loci in chronic Chagas cardiomyopathy. Chagas cardiomyopathy in Tripanosoma cruzi seropositivity 981 Latin American cases, 1,328 Latin American controls NA Illumina [8218190] (imputed) 3 Chagas cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0005529 GCST90026454 Genome-wide genotyping array 2021-10-22 34227697 Loesch DP 2021-07-06 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/34227697 Characterizing the Genetic Architecture of Parkinson's Disease in Latinos. Parkinson's disease 807 Latino cases, 690 Latino controls 1,234 Latino cases, 439,522 Latino controls Illumina [1240909] (imputed) 1 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90026456 Genome-wide genotyping array 2021-07-07 34006833 Elvsashagen T 2021-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34006833 The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Thalamus volume 30,114 white British ancestry individuals Affymetrix [8165723] (imputed) 7 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST012009 Genome-wide genotyping array 2021-07-07 34006833 Elvsashagen T 2021-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34006833 The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Anterior thalamic nuclei volume 30,114 white British ancestry individuals Affymetrix [8165723] (imputed) 3 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST012005 Genome-wide genotyping array 2021-07-07 34006833 Elvsashagen T 2021-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34006833 The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Lateral thalamic nuclei volume 30,114 white British ancestry individuals Affymetrix [8165723] (imputed) 11 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST012008 Genome-wide genotyping array 2021-07-07 34006833 Elvsashagen T 2021-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34006833 The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Ventral thalamic nuclei volume 30,114 white British ancestry individuals Affymetrix [8165723] (imputed) 5 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST012011 Genome-wide genotyping array 2021-07-07 34006833 Elvsashagen T 2021-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34006833 The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Intralaminar thalamic nuclei volume 30,114 white British ancestry individuals Affymetrix [8165723] (imputed) 12 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST012006 Genome-wide genotyping array 2021-07-07 34006833 Elvsashagen T 2021-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34006833 The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Medial thalamic nuclei volume 30,114 white British ancestry individuals Affymetrix [8165723] (imputed) 6 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST012010 Genome-wide genotyping array 2021-07-07 34006833 Elvsashagen T 2021-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34006833 The genetic architecture of the human thalamus and its overlap with ten common brain disorders. Posterior thalamic nuclei volume 30,114 white British ancestry individuals Affymetrix [8165723] (imputed) 6 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST012004 Genome-wide genotyping array 2021-08-27 33649182 Penova M 2021-03-01 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/33649182 Genome wide association study of HTLV-1-associated myelopathy/tropical spastic paraparesis in the Japanese population. HTLV-1 associated myelopathy 731 Japanese ancestry cases, 846 Japanese ancestry controls NA Illumina [126394] 8 tropical spastic paraparesis http://www.ebi.ac.uk/efo/EFO_0007527 GCST90026455 Genome-wide genotyping array 2021-11-17 33723576 Carrera C 2021-03-16 Brain www.ncbi.nlm.nih.gov/pubmed/33723576 Single nucleotide variations in ZBTB46 are associated with post-thrombolytic parenchymal haematoma. Parenchymal hematoma in thrombolytic-treated acute ischaemic stroke 71 European ancestry cases, 1,253 European ancestry controls 70 European ancestry cases, 510 European ancestry controls Illumina [7989272] (imputed) 6 parenchymal hematoma, response to recombinant tissue-plasminogen activator http://www.ebi.ac.uk/efo/EFO_0020101, http://www.ebi.ac.uk/efo/EFO_0600080 GCST90027882 Genome-wide genotyping array 2021-11-12 34154395 Brikell I 2021-06-22 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/34154395 Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD. Stimulant treatment initiation in ADHD 7,427 European ancestry cases, 1,706 European ancestry controls NA Illumina [6361597] (imputed) 0 stimulant use measurement http://www.ebi.ac.uk/efo/EFO_0600076 GCST90020214 Genome-wide genotyping array 2021-11-12 34154395 Brikell I 2021-06-22 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/34154395 Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD. Stimulant treatment discontinuation in ADHD 3,370 European ancestry cases, 3,854 European ancestry controls NA Illumina [6361597] (imputed) 0 stimulant use measurement http://www.ebi.ac.uk/efo/EFO_0600076 GCST90020215 Genome-wide genotyping array 2021-11-12 34154395 Brikell I 2021-06-22 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/34154395 Genetic, Clinical, and Sociodemographic Factors Associated With Stimulant Treatment Outcomes in ADHD. Switch to non-stimulant treatment in ADHD 1,137 European ancestry cases, 3,854 European ancestry controls NA Illumina [6361597] (imputed) 18 stimulant use measurement http://www.ebi.ac.uk/efo/EFO_0600076 GCST90020216 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (osmotic) Up to 7,586 non-Hispanic White ancestry individuals, Up to 1,049 East Asian ancestry individuals, Up to 257 South Asian ancestry individuals, Up to 1,046 African Americans individuals, Up to 456 Mexican and Central American Hispanics individuals, Up to 489 Caribbean Island Hispanics, Up to 1,336 individuals NA NR [14100000] (imputed) 14 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012135 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (oxidative) Up to 7,586 non-Hispanic White ancestry individuals, Up to 1,049 East Asian ancestry individuals, Up to 257 South Asian ancestry individuals, Up to 1,046 African Americans individuals, Up to 456 Mexican and Central American Hispanics individuals, Up to 489 Caribbean Island Hispanics, Up to 1,336 individuals NA NR [14100000] (imputed) 4 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012134 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (cold-storage) Up to 7,586 non-Hispanic White ancestry individuals, Up to 1,049 East Asian ancestry individuals, Up to 257 South Asian ancestry individuals, Up to 1,046 African Americans individuals, Up to 456 Mexican and Central American Hispanics individuals, Up to 489 Caribbean Island Hispanics, Up to 1,336 individuals NA NR [14100000] (imputed) 2 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012133 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (osmotic) Up to 456 Mexican and Central American Hispanics individuals, Up to 489 Caribbean Island Hispanics individuals NA NR [14100000] (imputed) 3 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012132 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (osmotic) Up to 1,049 East Asian ancestry individuals NA NR [14100000] (imputed) 2 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012131 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (osmotic) Up to 1,046 African Americans individuals NA NR [14100000] (imputed) 3 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012130 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (oxidative) Up to 1,046 African Americans individuals NA NR [14100000] (imputed) 1 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012129 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (cold-storage) Up to 7,586 non-Hispanic White ancestry individuals NA NR [14100000] (imputed) 1 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012128 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (oxidative) Up to 7,586 non-Hispanic White ancestry individuals NA NR [14100000] (imputed) 1 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012127 Genome-wide genotyping array 2021-07-27 34014839 Page GP 2021-05-20 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/34014839 Multi-ancestry genome-wide association study identifies 27 loci associated with measures of hemolysis following blood storage. hemolysis of donated blood (osmotic) Up to 7,586 non-Hispanic White ancestry individuals NA NR [14100000] (imputed) 14 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST012126 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_36:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060339 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_36:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060327 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol_36:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060322 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol-O_34:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060271 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol-O_38:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 6 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060370 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol-O_38:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060398 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol-O_40:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060419 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol-O_40:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060452 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol-O_42:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 6 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060470 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(32:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 273 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060760 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(34:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 55 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060707 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(34:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060704 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(35:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060720 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(35:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 24 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060715 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(36:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 59 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060759 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(36:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060757 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(36:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060750 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylglycerol(37:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90060767 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_33:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060425 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_34:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060458 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_34:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 6 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060449 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_34:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 36 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060444 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_35:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060478 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_35:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 10 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060469 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_36:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060501 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_36:0_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060502 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_36:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 42 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060495 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_36:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 28 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060498 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_36:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060516 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_36:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 35 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060492 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_36:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 23 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060488 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_38:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060535 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_38:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060533 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_38:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060532 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_38:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 34 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060521 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_38:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060525 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_38:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060542 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_38:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060518 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylinositol_40:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 12 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060548 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(44:6)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 20 diacylglycerol 44:6 measurement http://www.ebi.ac.uk/efo/EFO_0020070 GCST90060660 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Eicosanoid(C20H28O4)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90060128 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Eicosanoid(C20H30O3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90060122 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Eicosanoid(C20H32O3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90060123 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Eicosanoid(C20H33O3)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90060124 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(12:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060568 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(12:1)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060092 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(14:0)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060098 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(14:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060569 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(14:1)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060097 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Fatty acid(15:0)_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90060099 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidate(46:5_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidate measurement http://www.ebi.ac.uk/efo/EFO_0020047 GCST90060868 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_30:0_[M+H]1+/Phosphatidylethanolamine_33:0_[M+H]1+/Phosphatidate_35:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060242 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_30:1_[M-H]-/Phosphatidylethanolamine_33:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060236 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_31:2_[M+H]1+/Phosphatidylethanolamine_34:2_[M+H]1+/Phosphatidate_36:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 51 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060249 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_32:0_[M+H]1+/Phosphatidylethanolamine_35:0_[M+H]1+/Phosphatidate_37:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 40 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060270 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_32:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 19 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060372 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_32:1_[M+H]1+/Phosphatidylethanolamine_35:1_[M+H]1+/Phosphatidate_37:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060267 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_32:2_[M+H]1+/Phosphatidylethanolamine_35:2_[M+H]1+/Phosphatidate_37:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 32 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060264 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_32:2_[M+OAc]1-/Phosphatidylserine_36:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060359 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_33:1_[M+H]1+/Phosphatidylethanolamine_36:1_[M+H]1+/Phosphatidate_38:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060283 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_33:2_[M+H]1+/Phosphatidylethanolamine_36:2_[M+H]1+/Phosphatidate_38:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060278 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_33:2_[M+OAc]1-/Phosphatidylserine_37:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 9 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060387 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_33:3_[M+H]1+/Phosphatidylethanolamine_36:3_[M+H]1+/Phosphatidate_38:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060275 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_33:4_[M+H]1+/Phosphatidylethanolamine_36:4_[M+H]1+/Phosphatidate_38:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 34 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060273 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:0_[M+H]1+/Phosphatidylethanolamine_37:0_[M+H]1+/Phosphatidate_39:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 18 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060311 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:1_[M+H]1+/Phosphatidylethanolamine_37:1_[M+H]1+/Phosphatidate_39:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 17 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060307 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:1_[M+OAc]1-/Phosphatidylserine_38:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060415 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:2_[M+H]1+/Phosphatidylethanolamine_37:2_[M+H]1+/Phosphatidate_39:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 40 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060303 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:2_[M+OAc]1-/Phosphatidylserine_38:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 32 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060411 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:3_[M+H]1+/Phosphatidylethanolamine_37:3_[M+H]1+/Phosphatidate_39:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 29 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060298 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:3_[M+OAc]1-/Phosphatidylserine_38:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060406 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:4_[M+H]1+/Phosphatidylethanolamine_37:4_[M+H]1+/Phosphatidate_39:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060295 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_34:4_[M+OAc]1-/Phosphatidylserine_38:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060400 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:0_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060447 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine_35:1_[M+H]1+/Phosphatidylethanolamine_38:1_[M+H]1+/Phosphatidate_40:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060331 Genome-wide genotyping array 2022-05-10 35446358 He W 2022-04-21 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/35446358 Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging. Corneal resistance factor (MTAG) 123,734 European ancestry individuals NA NR [NR] (imputed) 369 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST90102517 Genome-wide genotyping array 2022-05-10 35446358 He W 2022-04-21 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/35446358 Association of Novel Loci With Keratoconus Susceptibility in a Multitrait Genome-Wide Association Study of the UK Biobank Database and Canadian Longitudinal Study on Aging. Central corneal thickness (MTAG) 17,803 European ancestry individuals NA NR [NR] (imputed) 233 central corneal thickness http://www.ebi.ac.uk/efo/EFO_0005213 GCST90102518 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(54:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 52 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060970 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(54:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 31 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060968 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(54:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 18 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060965 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(54:6)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060963 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(54:7)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060960 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(55:8)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060975 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(55:9)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060972 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(56:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90061001 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(56:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060999 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(56:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 48 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060997 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(56:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 58 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060994 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(56:6)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 120 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060991 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(56:7)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 51 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060987 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(57:10)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060998 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(57:11)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060996 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(57:9)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90061000 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(58:9)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 59 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90061006 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(59:11)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90061011 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(59:12)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90061010 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglyceroloxid(52:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060954 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglyceroloxid(53:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060973 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglyceroloxid(56:8)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90061003 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(48:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060852 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(48:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060847 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(49:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060876 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(49:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060871 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(49:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060866 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(50:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060900 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(50:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060897 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(50:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 16 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060894 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(50:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 23 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060889 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(50:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 18 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060886 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(51:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060919 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(51:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060915 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(51:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 18 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060911 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(51:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 14 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060906 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(52:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060941 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(52:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 25 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060940 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(52:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 20 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060937 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(52:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 44 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060934 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(52:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 23 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060932 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(52:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 12 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060927 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(52:6)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060923 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(53:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060955 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(53:3)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 48 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060952 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(53:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 19 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060948 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(54:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 7 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060974 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_54:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060538 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_54:7_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 13 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060536 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_55:8_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060546 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_55:9_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060543 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_56:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060556 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_56:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 26 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060554 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_56:6_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 39 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060553 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_56:7_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060551 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_56:8_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 19 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060550 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_57:11_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060555 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_58:10_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 27 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060559 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_58:7_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060564 Genome-wide genotyping array 2021-07-27 34054130 Bralten J 2021-05-30 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/34054130 Genetic underpinnings of sociability in the general population. Sociability score 342,461 European ancestry individuals NA Affymetrix [9327396] (imputed) 19 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST012114 Genome-wide genotyping array 2021-07-27 34054130 Bralten J 2021-05-30 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/34054130 Genetic underpinnings of sociability in the general population. Frequency of friend / family visits 342,461 European ancestry individuals NA Affymetrix [up to 9327396] (imputed) 1 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST012113 Genome-wide genotyping array 2021-07-27 34054130 Bralten J 2021-05-30 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/34054130 Genetic underpinnings of sociability in the general population. Attending social / leisure activities 342,461 European ancestry individuals NA Affymetrix [up to 9327396] (imputed) 1 social interaction measurement http://www.ebi.ac.uk/efo/EFO_0009592 GCST012112 Genome-wide genotyping array 2021-07-27 34054130 Bralten J 2021-05-30 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/34054130 Genetic underpinnings of sociability in the general population. Worry too long after an embarrassing experience 342,461 European ancestry individuals NA Affymetrix [up to 9327396] (imputed) 9 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST012111 Genome-wide genotyping array 2021-07-27 34054130 Bralten J 2021-05-30 Neuropsychopharmacology www.ncbi.nlm.nih.gov/pubmed/34054130 Genetic underpinnings of sociability in the general population. Loneliness 342,461 European ancestry individuals NA Affymetrix [up to 9327396] (imputed) 4 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST012110 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. Weight 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 12 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST012053 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. Waist circumference 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 9 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST012052 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. Systolic blood pressure 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 7 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST012051 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. Diastolic blood pressure 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 3 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST012050 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. High density lipoprotein cholesterol levels 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 6 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST012049 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. Triglyceride levels 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 33 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST012048 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. Fasting glucose 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 22 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST012047 Genome-wide genotyping array 2021-07-27 34074324 Wan JY 2021-06-01 Diabetol Metab Syndr www.ncbi.nlm.nih.gov/pubmed/34074324 Genome-wide association analysis of metabolic syndrome quantitative traits in the GENNID multiethnic family study. Fasting insulin 281 African American individuals from 73 families, 516 European ancestry individuals from 75 families, 125 Japanese American individuals from 15 families, 598 Mexican American individuals from 96 families NA Illumina [up to 13042663] (imputed) 7 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST012046 Genome-wide genotyping array 2021-06-24 34062886 Nazarian A 2021-05-01 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34062886 Genome-Wide Analysis of Sex Disparities in the Genetic Architecture of Lung and Colorectal Cancers. Lung cancer 237 European ancestry female cases, 220 European ancestry male cases, 8,354 European ancestry female controls, 6,278 European ancestry male controls NA NR [up to 1668434] (imputed) 12 lung cancer http://purl.obolibrary.org/obo/MONDO_0008903 GCST011974 Genome-wide genotyping array 2021-06-24 34062886 Nazarian A 2021-05-01 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34062886 Genome-Wide Analysis of Sex Disparities in the Genetic Architecture of Lung and Colorectal Cancers. Colorectal cancer 211 European ancestry female cases, 186 European ancestry male cases, 8,382 European ancestry female controls, 6,312 European ancestry male controls NA NR [up to 1668415] (imputed) 7 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST011973 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_58:8_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 14 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060562 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_58:9_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060561 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_59:11_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060566 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_59:12_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060565 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(39:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060651 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(44:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060741 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(44:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060736 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(46:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060802 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(46:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060797 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(46:2)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060792 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(47:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060823 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(48:0)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060858 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol(48:1)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060856 Genome-wide genotyping array 2021-06-30 34052317 Li M 2021-05-28 Genomics www.ncbi.nlm.nih.gov/pubmed/34052317 A next generation sequencing combined genome-wide association study identifies novel tuberculosis susceptibility loci in Chinese population. Tuberculosis 29 Chinese ancestry cases, 77 Chinese ancestry controls 569 Chinese ancestry cases, 534 Chinese ancestry controls Illumina [152523] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST011980 Genome-wide genotyping array 2021-08-13 34302048 Qu HQ 2021-07-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34302048 Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci. Type 1 diabetes with low genetic risk score 957 European ancestry cases, 12,323 European ancestry controls NA Illumina [104689647] (imputed) 149 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90000181 Genome-wide genotyping array 2021-08-13 34302048 Qu HQ 2021-07-23 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34302048 Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci. Type 1 diabetes 6,599 European ancestry cases, 12,323 European ancestry controls NA Illumina [104689647] (imputed) 113 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST012179 Genome-wide genotyping array 2021-12-02 34593835 Takahashi Y 2021-09-30 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34593835 A genome-wide association study identifies a novel candidate locus at the DLGAP1 gene with susceptibility to resistant hypertension in the Japanese population. Resistant hypertension 2,705 Japanese ancestry cases, 21,296 Japanese ancestry controls NA Illumina [7199488] (imputed) 18 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST90058972 Genome-wide genotyping array 2021-12-07 34639784 Chen TH 2021-10-06 Int J Environ Res Public Health www.ncbi.nlm.nih.gov/pubmed/34639784 The Mediation Effects of Aluminum in Plasma and Dipeptidyl Peptidase Like Protein 6 (DPP6) Polymorphism on Renal Function via Genome-Wide Typing Association. Aluminium levels 494 Han Chinese ancestry individuals NA NR [615681] 3 blood aluminium measurement http://www.ebi.ac.uk/efo/EFO_0007575 GCST90061020 Genome-wide genotyping array 2021-10-08 34002096 Mullins N 2021-05-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34002096 Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Bipolar disorder 41,917 European ancestry cases, 371,549 European ancestry controls NA Affymetrix, Illumina [7549318] (imputed) 64 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST012465 Genome-wide genotyping array 2021-10-08 34002096 Mullins N 2021-05-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34002096 Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Bipolar I disorder 25,060 European ancestry cases, 449,978 European ancestry controls NA Affymetrix, Illumina [7549318] (imputed) 44 bipolar I disorder http://www.ebi.ac.uk/efo/EFO_0009963 GCST012464 Genome-wide genotyping array 2021-10-08 34002096 Mullins N 2021-05-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34002096 Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. Bipolar II disorder 6,781 European ancestry cases, 364,075 European ancestry controls NA Affymetrix, Illumina [7549318] (imputed) 1 bipolar II disorder http://www.ebi.ac.uk/efo/EFO_0009964 GCST012463 Genome-wide genotyping array 2021-06-09 34012061 Sipeky C 2021-05-19 Prostate Cancer Prostatic Dis www.ncbi.nlm.nih.gov/pubmed/34012061 Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease. Prostate cancer 2,738 Finnish ancestry cases, 2,400 Finnish ancestry controls NA Illumina [185478] 21 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST011829 Genome-wide genotyping array 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Two-hour glucose 1,431 African American individuals NA Affymetrix, Illumina [22935934] (imputed) 0 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST90002225 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Two-hour glucose 8,509 East Asian ancestry individuals NA Affymetrix [9187953] (imputed) 1 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST90002226 Genome-wide genotyping array 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Two-hour glucose 63,396 European ancestry individuals NA Affymetrix, Illumina [30098705] (imputed) 17 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST90002227 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Two-hour glucose 12,578 Hispanic individuals NA Illumina [24662309] (imputed) 4 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST90002228 Genome-wide genotyping array 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Two-hour glucose 1,431 African American individuals, 8,509 East Asian ancestry individuals, 63,396 European ancestry individuals, 12,578 Hispanic individuals NA Affymetrix, Illumina [38654120] (imputed) 0 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST90002229 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting glucose 16,579 African American individuals NA Affymetrix, Illumina [27843817] (imputed) 11 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90002230 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting glucose 35,619 East Asian ancestry individuals NA Affymetrix, Illumina [15438438] (imputed) 15 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90002231 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting glucose 200,622 European ancestry individuals NA Affymetrix, Illumina [34064007] (imputed) 92 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90002232 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting glucose 19,247 Hispanic individuals NA Affymetrix, Illumina [28177426] (imputed) 13 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90002233 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting glucose 9,343 South Asian ancestry individuals NA Illumina, Perlegen [20274841] (imputed) 9 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90002234 Genome-wide genotyping array 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting glucose 16,579 African American individuals, 35,619 East Asian ancestry individuals, 20,0622 European ancestry individuals, 19,247 Hispanic individuals, 9,343 South Asian ancestry individuals NA Affymetrix, Illumina, Perlegen [42673998] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90002235 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting insulin 8,101 African American individuals NA Affymetrix, Illumina [26320006] (imputed) 2 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90002236 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting insulin 29,792 East Asian ancestry individuals NA Affymetrix, Illumina [14733249] (imputed) 1 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90002237 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting insulin 151,013 European ancestry individuals NA Affymetrix, Illumina [32635793] (imputed) 54 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90002238 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting insulin 16,386 Hispanic individuals NA Affymetrix, Illumina [26195808] (imputed) 8 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90002239 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting insulin 8,353 South Asian ancestry individuals NA Illumina, Perlegen [20092343] (imputed) 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90002240 Genome-wide genotyping array 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Fasting insulin 8,101 African American individuals, 29,792 East Asian ancestry individuals, 151,013 European ancestry individuals, 16,386 Hispanic individuals, 8,353 South Asian ancestry individuals NA Affymetrix, Illumina, Perlegen [41471552] (imputed) 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90002241 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Glycated hemoglobin levels 6,647 African American individuals NA Affymetrix, Illumina [26614666] (imputed) 5 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90002242 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Glycated hemoglobin levels 33,307 East Asian ancestry individuals NA Affymetrix, Illumina [15728197] (imputed) 27 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90002243 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Glycated hemoglobin levels 146,806 European ancestry individuals NA Affymetrix, Illumina [33811881] (imputed) 113 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90002244 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Glycated hemoglobin levels 15,248 Hispanic individuals NA Affymetrix, Illumina [29199641] (imputed) 13 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90002245 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Glycated hemoglobin levels 9,525 South Asian ancestry individuals NA Illumina, Perlegen [19922415] (imputed) 3 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90002246 Genome-wide genotyping array 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Glycated hemoglobin levels 6,647 African American individuals, 33,307 East Asian ancestry individuals, 146,806 European ancestry individuals, 15,248 Hispanic individuals, 9,525 South Asian ancestry individuals, 4,441 Sub-Saharan African ancestry individuals NA Affymetrix, Illumina, Perlegen [43540446] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90002247 Genome-wide genotyping array, Targeted genotyping array [Genome-wide genotyping array|Metabochip] 2021-06-10 34059833 Chen J 2021-05-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34059833 The trans-ancestral genomic architecture of glycemic traits. Glycated hemoglobin levels 4,441 Sub-Saharan African ancestry individuals NA NR [19426848] (imputed) 2 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90002248 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(42:9)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060807 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(43:2)_[M-CH3]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 58 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060831 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(44:9)_[M+H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 147 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060859 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Sphingomyelin(46:1)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90060929 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_44:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060314 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_45:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 37 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060333 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_46:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060380 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_46:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060376 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_46:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060373 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_46:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060369 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_46:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 10 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060362 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_46:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 20 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060356 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_47:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060396 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_47:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060391 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_48:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060430 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_48:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060424 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_48:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060421 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_48:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060418 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_48:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060412 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_49:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060453 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_49:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060448 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_49:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060443 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_49:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060440 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_49:5_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060438 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Triacylglycerol_50:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90060484 Genome-wide genotyping array 2022-03-04 33993232 Carmona EG 2021-05-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/33993232 Identification of a shared genetic risk locus for Kawasaki disease and IgA vasculitis by a cross-phenotype meta-analysis. Kawasaki disease or immunoglobulin A vasculitis (pleiotropy) 402 European ancestry Kawasaki disease cases, 215 European ancestry IgAV cases, 7,538 European ancestry controls 186 East Asian ancestry Kawasaki disease cases, 600 East Asian ancestry controls, 384 IgAV European or unknown ancestry cases, 3,126 European or unknown ancestry controls Illumina [5690841] (imputed) 3 mucocutaneous lymph node syndrome, vasculitis http://www.ebi.ac.uk/efo/EFO_0004246, http://www.ebi.ac.uk/efo/EFO_0006803 GCST90095078 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Height 2,603 Korean ancestry males, 2,869 Korean ancestry females 19,571 Korean ancestry males, 37,321 Korean ancestry females NR [8056211] (imputed) 67 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST011972 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Weight 2,603 Korean ancestry males, 2,869 Korean ancestry females 19,571 Korean ancestry males, 37,321 Korean ancestry females NR [8056211] (imputed) 21 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST011971 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Body mass index 5,472 Korean ancestry individuals 56,892 Korean ancestry individuals NR [8056211] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST011970 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Waist circumference 5,472 Korean ancestry individuals 56,892 Korean ancestry individuals NR [8056211] (imputed) 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST011969 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Hip circumference 5,472 Korean ancestry individuals 56,892 Korean ancestry individuals NR [8056211] (imputed) 0 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST011968 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Waist-hip ratio 2,603 Korean ancestry males, 2,869 Korean ancestry females 19,571 Korean ancestry males, 37,321 Korean ancestry females NR [8056211] (imputed) 1 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST011967 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Waist circumference adjusted for body mass index 5,472 Korean ancestry individuals 56,892 Korean ancestry individuals NR [8056211] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST011966 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Hip circumference adjusted for BMI 5,472 Korean ancestry individuals 56,892 Korean ancestry individuals NR [8056211] (imputed) 0 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST011965 Genome-wide genotyping array 2021-06-24 34054925 Cho HW 2021-05-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/34054925 A Genome-Wide Association Study of Novel Genetic Variants Associated With Anthropometric Traits in Koreans. Waist-to-hip ratio adjusted for BMI 2,603 Korean ancestry males, 2,869 Korean ancestry females 19,571 Korean ancestry males, 37,321 Korean ancestry females NR [8056211] (imputed) 5 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST011964 Genome-wide genotyping array 2021-10-07 34512620 Matzaraki V 2021-08-26 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34512620 Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. Candida albicans stimulated MCP-2 levels 378 European ancestry individuals NA Illumina [NR] (imputed) 1 monocyte chemotactic protein-2 measurement http://www.ebi.ac.uk/efo/EFO_0010789 GCST90038445 Genome-wide genotyping array 2021-10-07 34512620 Matzaraki V 2021-08-26 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34512620 Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. Candida albicans stimulated CCL3 levels 378 European ancestry individuals NA Illumina [NR] (imputed) 2 CCL3 measurement http://www.ebi.ac.uk/efo/EFO_0010770 GCST90038446 Genome-wide genotyping array 2021-10-07 34512620 Matzaraki V 2021-08-26 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34512620 Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. Candida albicans stimulated MMP-1 levels 378 European ancestry individuals NA Illumina [NR] (imputed) 1 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90038447 Genome-wide genotyping array 2021-10-07 34512620 Matzaraki V 2021-08-26 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34512620 Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. Candida albicans stimulated IL-8 levels 378 European ancestry individuals NA Illumina [NR] (imputed) 1 interleukin 8 measurement http://www.ebi.ac.uk/efo/EFO_0008191 GCST90038448 Genome-wide genotyping array 2021-10-07 34512620 Matzaraki V 2021-08-26 Front Immunol www.ncbi.nlm.nih.gov/pubmed/34512620 Inflammatory Protein Profiles in Plasma of Candidaemia Patients and the Contribution of Host Genetics to Their Variability. Survival in candidemia 52 European ancestry cases, 104 European ancestry controls NA Illumina [5450489] (imputed) 0 survival time, Candidemia http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_1001282 GCST90038449 Genome-wide genotyping array 2021-10-08 34069769 Al-Sarraj Y 2021-05-18 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34069769 Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families. Autism spectrum disorder 487 Middle Eastern ancestry individuals from 171 families NA Illumina [516320] 7 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST012466 Genome-wide genotyping array 2021-10-07 34122051 Wang H 2021-05-28 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/34122051 Similar Genetic Architecture of Alzheimer's Disease and Differential APOE Effect Between Sexes. Alzheimer's disease 4,010 European ancestry cases, 4,672 European ancestry controls NA NR [38043082] (imputed) 8 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90038451 Genome-wide genotyping array 2021-10-07 34122051 Wang H 2021-05-28 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/34122051 Similar Genetic Architecture of Alzheimer's Disease and Differential APOE Effect Between Sexes. Alzheimer's disease 5,705 European ancestry cases, 7,067 European ancestry controls NA NR [38043082] (imputed) 19 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90038452 Genome-wide genotyping array 2022-01-31 34011927 Park JH 2021-05-19 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34011927 Novel Alzheimer's disease risk variants identified based on whole-genome sequencing of APOE ε4 carriers. Alzheimer's disease in APOE e4+ carriers 331 Korean ancestry cases, 169 Korean ancestry controls 190 Korean ancestry cases, 97 Korean ancestry controls Illumina [22526987] 2 Alzheimer disease, APOE carrier status http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0007659 GCST90093315 Genome-wide sequencing 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (trunk fat ratio) 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044720 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android fat/gynoid fat ratio 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044721 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk fat/peripheral fat ratio 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044722 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android total mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044723 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid total mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044724 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm total mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 2 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044725 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg total mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 2 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044726 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk total mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044727 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total bone mineral content 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044728 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total fat mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044729 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total lean mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044730 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044731 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android fat mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044732 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid fat mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 2 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044733 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm fat mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044734 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg fat mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 3 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044735 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk fat mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044736 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Visceral adipose tissue mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90044737 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Visceral adipose tissue volume 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90044738 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android lean mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044739 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid lean mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044740 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm lean mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044741 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg lean mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044742 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk lean mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044743 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android bone mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST90044744 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg total mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026443 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk total mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026444 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total bone mineral content 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90026445 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total fat mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90026446 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total lean mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026447 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total mass 2,294 White British ancestry female individuals, 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90026448 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android fat mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044701 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid fat mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044702 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm fat mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 1 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044703 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg fat mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044704 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk fat mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044705 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Visceral adipose tissue mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90044706 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Visceral adipose tissue volume 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90044707 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android lean mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044708 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid lean mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044709 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm lean mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044710 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg lean mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044711 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk lean mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044712 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android bone mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST90044713 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid bone mass 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 1 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST90044714 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm bone mineral content 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044715 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg bone mineral content 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044716 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk bone mineral content 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 1 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044717 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (arm fat ratio) 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044718 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (leg fat ratio) 2,294 White British ancestry female individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044719 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid bone mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 bone measurement http://www.ebi.ac.uk/efo/EFO_0004512 GCST90044745 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm bone mineral content 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044746 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg bone mineral content 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044747 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk bone mineral content 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044748 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (arm fat ratio) 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044749 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (leg fat ratio) 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044750 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Body fat distribution (trunk fat ratio) 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044751 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android fat/gynoid fat ratio 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 1 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044752 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk fat/peripheral fat ratio 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 body fat distribution http://www.ebi.ac.uk/efo/EFO_0004341 GCST90044753 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Android total mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044754 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Gynoid total mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044755 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Arm total mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044756 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Leg total mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044757 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Trunk total mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044758 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total bone mineral content 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone mineral content measurement http://www.ebi.ac.uk/efo/EFO_0007621 GCST90044759 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total fat mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90044760 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total lean mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044761 Genome-wide genotyping array 2021-10-08 34239500 Livingstone KM 2021-06-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/34239500 Discovery Genome-Wide Association Study of Body Composition in 4,386 Adults From the UK Biobank's Pilot Imaging Enhancement Study. Total mass 2,109 White British ancestry male individuals NA NR [6137607] (imputed) 0 bone measurement, fat body mass, lean body mass http://www.ebi.ac.uk/efo/EFO_0004512, http://www.ebi.ac.uk/efo/EFO_0005409, http://www.ebi.ac.uk/efo/EFO_0004995 GCST90044762 Genome-wide genotyping array 2021-10-18 34021356 Sarnowski C 2021-05-22 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/34021356 Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche. Menarche (age at onset) 19,028 African ancestry individuals 5,148 African ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST012491 Genome-wide genotyping array 2021-10-18 34021356 Sarnowski C 2021-05-22 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/34021356 Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche. Menarche (age at onset) 19,028 African ancestry individuals, 3,205 South Asian ancestry individuals, 2,095 East Asian ancestry individuals, 10,661 Hispanic/Latina individuals, 3,557 individuals NA Affymetrix, Illumina [NR] (imputed) 7 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST012492 Genome-wide genotyping array 2021-08-13 34319593 Li N 2021-07-28 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34319593 Genetic variants of CYP4F12 gene are associated with glioma susceptibility. Glioma 485 Han Chinese ancestry cases, 485 Han Chinese ancestry controls NA Affymetrix [4635191] (imputed) 2 glioma http://www.ebi.ac.uk/efo/EFO_0005543 GCST90020047 Genome-wide genotyping array 2021-07-07 34127860 Robertson CC 2021-06-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34127860 Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes. Type 1 diabetes 20,065 European ancestry cases, 33,065 European ancestry controls, 1,045 other-admixed ancestry cases, 1,103 other-admixed ancestry controls, 1,043 African ancestry cases, 3,206 African ancestry controls NA Illumina [715631] (imputed) 72 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90013445 Targeted genotyping array [ImmunoChip] 2021-07-07 34127860 Robertson CC 2021-06-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34127860 Fine-mapping, trans-ancestral and genomic analyses identify causal variants, cells, genes and drug targets for type 1 diabetes. Type 1 diabetes 13,458 non-Finnish Europeans ancestry cases, 20,143 non-Finnish Europeans ancestry controls NA Illumina [715631] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90013446 Targeted genotyping array [ImmunoChip] 2021-10-04 34014961 Palmer ND 2021-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/34014961 Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study. Serum 25-Hydroxyvitamin D levels in type 2 diabetes 697 African American individuals 554 African American individuals Illumina [3436913] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST012428 Genome-wide genotyping array 2021-10-04 34014961 Palmer ND 2021-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/34014961 Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study. 1,25-dihydroxycholecalciferol levels in type 2 diabetes 697 African American individuals 554 African American individuals Illumina [3436913] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST012427 Genome-wide genotyping array 2021-10-04 34014961 Palmer ND 2021-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/34014961 Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study. Serum vitamin D-binding protein levels in type 2 diabetes 697 African American individuals NA Illumina [3436913] (imputed) 3 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST012426 Genome-wide genotyping array 2021-10-04 34014961 Palmer ND 2021-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/34014961 Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study. Bioavailable vitamin D levels in type 2 diabetes 697 African American individuals NA Illumina [3436913] (imputed) 1 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST012425 Genome-wide genotyping array 2021-10-04 34014961 Palmer ND 2021-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/34014961 Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study. Intact parathyroid hormone levels in type 2 diabetes 697 African American individuals NA Illumina [3436913] (imputed) 0 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST012424 Genome-wide genotyping array 2021-10-04 34014961 Palmer ND 2021-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/34014961 Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study. Thoracic volumetric BMD in type 2 diabetes 697 African American individuals NA Illumina [3436913] (imputed) 0 volumetric bone mineral density http://www.ebi.ac.uk/efo/EFO_0007620 GCST012423 Genome-wide genotyping array 2021-10-04 34014961 Palmer ND 2021-05-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/34014961 Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study. Lumbar volumetric BMD in type 2 diabetes 697 African American individuals NA Illumina [3436913] (imputed) 0 volumetric bone mineral density http://www.ebi.ac.uk/efo/EFO_0007620 GCST012422 Genome-wide genotyping array 2021-10-22 34151794 Kang S 2021-06-18 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/34151794 Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study. Late-onset Alzheimer's disease 1,119 Korean ancestry cases, 1,172 Korean ancestry controls 980 Japanese ancestry cases, 976 Japanese ancestry controls NR [35685761] (imputed) 1 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST90026599 Genome-wide genotyping array 2021-10-22 34151794 Kang S 2021-06-18 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/34151794 Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study. Late-onset Alzheimer’s disease in APOEe4 carriers 498 Korean ancestry cases, 196 Korean ancestry controls 545 Japanese ancestry cases, 161 Japanese ancestry controls NR [NR] (imputed) 0 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST90026600 Genome-wide genotyping array 2021-10-22 34151794 Kang S 2021-06-18 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/34151794 Potential Novel Genes for Late-Onset Alzheimer's Disease in East-Asian Descent Identified by APOE-Stratified Genome-Wide Association Study. Late-onset Alzheimer’s disease in APOEe4 non-carriers 621 Korean ancestry cases, 976 Korean ancestry controls 435 Japanese ancestry cases, 815 Japanese ancestry controls NR [NR] (imputed) 2 late-onset Alzheimers disease http://www.ebi.ac.uk/efo/EFO_1001870 GCST90026601 Genome-wide genotyping array 2021-10-06 34154648 Kim HR 2021-06-21 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/34154648 Identifying novel genetic variants for brain amyloid deposition: a genome-wide association study in the Korean population. Amyloid beta positivity 629 Korean ancestry cases, 561 Korean ancestry controls 104 Korean ancestry cases, 180 Korean ancestry controls Illumina [4906407] (imputed) 4 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST012459 Genome-wide genotyping array 2022-01-05 34311721 Alotaibi RN 2021-07-26 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/34311721 Genome-Wide Association Study (GWAS) of dental caries in diverse populations. Primary dental caries (decayed and filled teeth) 1,116 children NA Illumina [8859951] (imputed) 6 primary dental caries http://www.ebi.ac.uk/efo/EFO_0600095 GCST90027027 Genome-wide genotyping array 2022-01-05 34311721 Alotaibi RN 2021-07-26 BMC Oral Health www.ncbi.nlm.nih.gov/pubmed/34311721 Genome-Wide Association Study (GWAS) of dental caries in diverse populations. Permanent dental caries (decayed and filled teeth) 2,570 adults NA Illumina [8859951] (imputed) 6 permanent dental caries http://www.ebi.ac.uk/efo/EFO_0600096 GCST90027028 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to phenytoin in focal epilepsy 71 European ancestry cases, 218 European ancestry controls NA Illumina [NR] (imputed) 4 response to phenytoin http://www.ebi.ac.uk/efo/EFO_0006345 GCST90020117 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to calcium-channel-Active anticonvulsants in focal epilepsy 214 European ancestry cases, 410 European ancestry controls NA Illumina [NR] (imputed) 3 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020118 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to valproic acid in focal epilepsy 202 European ancestry cases, 528 European ancestry controls NA Illumina [NR] (imputed) 3 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020119 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to levetiracetam in epilepsy 343 European ancestry cases, 895 European ancestry controls NA Illumina [NR] (imputed) 2 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020120 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to lamotrigine in epilepsy 471 European ancestry cases, 929 European ancestry controls NA Illumina [NR] (imputed) 4 response to lamotrigine http://www.ebi.ac.uk/efo/EFO_0007661 GCST90020121 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to calcium-channel-Active anticonvulsants in epilepsy 690 European ancestry cases, 848 European ancestry controls NA Illumina [NR] (imputed) 1 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020122 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to valproic acid in epilepsy 612 European ancestry cases, 690 European ancestry controls NA Illumina [NR] (imputed) 1 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020123 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to sodium channel-Active anticonvulsants in focal epilepsy 636 European ancestry cases, 890 European ancestry controls NA Illumina [NR] (imputed) 0 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020124 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to levetiracetam in focal epilepsy 258 European ancestry cases, 678 European ancestry controls NA Illumina [NR] (imputed) 3 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020112 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to sodium channel-Active anticonvulsant in focal epilepsy 910 European ancestry cases, 1,286 European ancestry controls NA Illumina [NR] (imputed) 2 response to anticonvulsant http://purl.obolibrary.org/obo/GO_0036277 GCST90020113 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to lamotrigine in focal epilepsy 334 European ancestry cases, 680 European ancestry controls NA Illumina [NR] (imputed) 3 response to lamotrigine http://www.ebi.ac.uk/efo/EFO_0007661 GCST90020114 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to carbamazepine in focal epilepsy 424 European ancestry cases, 591 European ancestry controls NA Illumina [NR] (imputed) 3 response to carbamazepine http://www.ebi.ac.uk/efo/EFO_0008484 GCST90020115 Genome-wide genotyping array 2021-07-29 34177598 Wolking S 2021-06-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/34177598 Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications. Response to oxcarbazepine in focal epilepsy 98 European ancestry cases, 296 European ancestry controls NA Illumina [NR] (imputed) 4 response to oxcarbazepine http://www.ebi.ac.uk/efo/EFO_0009893 GCST90020116 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Progression free survival in epithelial ovarian cancer treated with carboplatin and paclitaxel 2,352 European ancestry individuals NA Illumina [12764477] (imputed) 34 progression free survival, response to carboplatin, methylcobalamin deficiency type cblE, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0004920, http://purl.obolibrary.org/obo/GO_0097328, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0001075 GCST012474 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Progression free survival in epithelial ovarian cancer 5,596 European ancestry individuals NA Illumina [12770451] (imputed) 19 progression free survival, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0004920, http://www.ebi.ac.uk/efo/EFO_0001075 GCST012473 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Progression free survival in serous epithelial ovarian cancer treated with carboplatin and paclitaxel 1,751 European ancestry individuals NA Illumina [12759548] (imputed) 36 progression free survival, response to carboplatin, methylcobalamin deficiency type cblE, ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_0004920, http://purl.obolibrary.org/obo/GO_0097328, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_1001516 GCST012472 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Progression free survival in serous epithelial ovarian cancer 4,037 European ancestry individuals NA Illumina [12770451] (imputed) 23 progression free survival, ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_0004920, http://www.ebi.ac.uk/efo/EFO_1001516 GCST012471 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Overall survival in epithelial ovarian cancer treated with carboplatin and paclitaxel 2,620 European ancestry individuals NA Illumina [12765645] (imputed) 0 response to carboplatin, methylcobalamin deficiency type cblE, overall survival, ovarian carcinoma http://purl.obolibrary.org/obo/GO_0097328, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0001075 GCST012470 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Overall survival in epithelial ovarian cancer 6,160 European ancestry individuals NA Illumina [12770750] (imputed) 0 overall survival, ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0001075 GCST012469 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Overall survival in serous epithelial ovarian cancer treated with paclitaxel and cisplatin 1,901 European ancestry individuals NA Illumina [12761635] (imputed) 0 response to carboplatin, methylcobalamin deficiency type cblE, overall survival, ovarian serous carcinoma http://purl.obolibrary.org/obo/GO_0097328, http://purl.obolibrary.org/obo/MONDO_0009354, http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1001516 GCST012468 Genome-wide genotyping array 2021-10-08 34162658 Quinn MC 2021-06-23 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/34162658 Identification of a locus near ULK1 associated with progression-free survival in ovarian cancer. Overall survival in serous epithelial ovarian cancer 4,391 European ancestry individuals NA Illumina [12769717] (imputed) 0 overall survival, ovarian serous carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1001516 GCST012467 Genome-wide genotyping array 2021-10-20 34076728 Zhang YM 2021-06-02 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/34076728 Shared genetic study gives insights into the shared and distinct pathogenic immunity components of IgA nephropathy and SLE. IgA nephropathy 1,180 East Asian ancestry cases, 899 East Asian ancestry controls NA Illumina [NR] (imputed) 7 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST90020041 Genome-wide genotyping array 2021-10-20 34076728 Zhang YM 2021-06-02 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/34076728 Shared genetic study gives insights into the shared and distinct pathogenic immunity components of IgA nephropathy and SLE. Systemic lupus erythematosus 1,639 East Asian ancestry cases, 2,410 East Asian ancestry controls NA Illumina [NR] (imputed) 39 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90020042 Genome-wide genotyping array 2021-07-27 34106200 Machipisa T 2021-06-09 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/34106200 Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study. Rheumatic heart disease 601 European ancestry, South East Asian ancestry, South Asian ancestry, African ancestry and South African ancestry cases, 454 European ancestry, South East Asian ancestry, South Asian ancestry, African ancestry and South African ancestry controls NA Illumina [7605010] (imputed) 6 rheumatic heart disease http://www.ebi.ac.uk/efo/EFO_1001161 GCST012116 Genome-wide genotyping array 2021-07-27 34106200 Machipisa T 2021-06-09 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/34106200 Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study. Rheumatic heart disease 1,687 Sub-Saharan African ancestry and African ancestry cases, 1,492 Sub-Saharan African ancestry and African ancestry controls, 601 European ancestry, South East Asian ancestry, South Asian ancestry, African ancestry and South African ancestry cases, 454 European ancestry, South East Asian ancestry, South Asian ancestry, African ancestry and South African ancestry controls NA Illumina [7605010] (imputed) 6 rheumatic heart disease http://www.ebi.ac.uk/efo/EFO_1001161 GCST012115 Genome-wide genotyping array 2021-07-27 34106200 Machipisa T 2021-06-09 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/34106200 Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study. Rheumatic heart disease 1,687 Sub-Saharan African ancestry and African ancestry cases, 1,492 Sub-Saharan African ancestry and African ancestry controls NA Illumina [7605010] (imputed) 6 rheumatic heart disease http://www.ebi.ac.uk/efo/EFO_1001161 GCST012117 Genome-wide genotyping array 2022-06-15 35275946 Engoren M 2022-03-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/35275946 Genetic variants associated with sepsis. Sepsis-2 2,040 European or unknown ancestry individuals NA Illumina [14000000] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90104583 Genome-wide genotyping array 2022-06-15 35275946 Engoren M 2022-03-11 PLoS One www.ncbi.nlm.nih.gov/pubmed/35275946 Genetic variants associated with sepsis. Sepsis-3 1,295 European or unknown ancestry individuals NA Illumina [14000000] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90104584 Genome-wide genotyping array 2021-06-11 33987465 Alfradique-Dunham I 2021-01-28 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/33987465 Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes. Parkinson's disease motor subtype (tremor dominant vs postural instability/gait difficulty) 1,570 European ancestry tremor dominant cases, 1,259 European ancestry postural instability/gait difficulty cases NA Illumina [12910578] (imputed) 7 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90000014 Genome-wide genotyping array 2021-06-11 33987465 Alfradique-Dunham I 2021-01-28 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/33987465 Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes. Parkinson's disease motor subtype (tremor to postural instability/gait difficulty score ratio) 3,212 European ancestry individuals NA Illumina [14638245] (imputed) 31 Parkinson's disease symptom measurement http://www.ebi.ac.uk/efo/EFO_0600011 GCST90000015 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Esterified brassicasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 esterified brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0020960 GCST90101765 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free brassicasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0020959 GCST90101766 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free to esterified brassicasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free brassicasterol measurement, esterified brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0020959, http://www.ebi.ac.uk/efo/EFO_0020960 GCST90101767 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free brassicasterol to free cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free cholesterol measurement, free brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0020959 GCST90101768 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free brassicasterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 1 free lanosterol measurement, free brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020959 GCST90101769 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total brassicasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 total brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0020958 GCST90101770 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total brassicasterol to total cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 total cholesterol measurement, total brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0020958 GCST90101771 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total brassicasterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free lanosterol measurement, total brassicasterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020958 GCST90101772 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Esterified campesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 esterified campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020964 GCST90101773 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free campesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020963 GCST90101774 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free campesterol to esterified campesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 esterified campesterol measurement, free campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020964, http://www.ebi.ac.uk/efo/EFO_0020963 GCST90101775 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free campesterol to free cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free cholesterol measurement, free campesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0020963 GCST90101776 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free campesterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free lanosterol measurement, free campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020963 GCST90101777 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total campesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 2 total campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020962 GCST90101778 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total campesterol to total cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 total cholesterol measurement, total campesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0020962 GCST90101779 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total campesterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free lanosterol measurement, total campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020962 GCST90101780 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Esterified sitosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 esterified sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0020967 GCST90101781 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free sitosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0020966 GCST90101782 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free sitosterol to free cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free cholesterol measurement, free sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0020966 GCST90101783 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free sitosterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free lanosterol measurement, free sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020966 GCST90101784 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free sitosterol to esterified sitosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free sitosterol measurement, esterified sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0020966, http://www.ebi.ac.uk/efo/EFO_0020967 GCST90101785 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total sitosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 3 total sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0020965 GCST90101786 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total sitosterol to total cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 total cholesterol measurement, total sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0020965 GCST90101787 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total sitosterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free lanosterol measurement, total sitosterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020965 GCST90101788 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Esterified stigmasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 1 esterified stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0020970 GCST90101789 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free stigmasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0020969 GCST90101790 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free stigmasterol to free cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free cholesterol measurement, free stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0020969 GCST90101791 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free stigmasterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free lanosterol measurement, free stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020969 GCST90101792 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Free stigmasterol to esterified stigmasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free stigmasterol measurement, esterified stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0020969, http://www.ebi.ac.uk/efo/EFO_0020970 GCST90101793 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total stigmasterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 total stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0020968 GCST90101794 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total stigmasterol to total cholesterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 total cholesterol measurement, total stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0020968 GCST90101795 Genome-wide genotyping array 2022-04-22 35013273 Scholz M 2022-01-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35013273 Genome-wide meta-analysis of phytosterols reveals five novel loci and a detrimental effect on coronary atherosclerosis. Total stigmasterol to free lanosterol 9,758 European ancestry individuals NA Affymetrix, Illumina [8000000] (imputed) 0 free lanosterol measurement, total stigmasterol measurement http://www.ebi.ac.uk/efo/EFO_0020961, http://www.ebi.ac.uk/efo/EFO_0020968 GCST90101796 Genome-wide genotyping array 2021-07-27 34187846 Ong JS 2021-06-29 Gut www.ncbi.nlm.nih.gov/pubmed/34187846 Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis. Gastroesophageal reflux disease 129,080 European ancestry cases, 473,524 European ancestry controls 462,753 cases, 1,127,474 controls NR [2324712] (imputed) 37 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90000514 Genome-wide genotyping array 2021-07-27 34187846 Ong JS 2021-06-29 Gut www.ncbi.nlm.nih.gov/pubmed/34187846 Multitrait genetic association analysis identifies 50 new risk loci for gastro-oesophageal reflux, seven new loci for Barrett's oesophagus and provides insights into clinical heterogeneity in reflux diagnosis. Barrett's esophagus 13,358 European ancestry cases, 43,071 European ancestry controls 24,099 cases, 1,484,025 controls NR [2324712] (imputed) 8 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90000515 Genome-wide genotyping array 2021-07-28 34177493 Mountford HS 2021-06-09 Front Hum Neurosci www.ncbi.nlm.nih.gov/pubmed/34177493 Genome-Wide Association Study of Motor Coordination. Motor coordination 4,542 European ancestry children NA Illumina [4774020] (imputed) 7 motor function measurement http://www.ebi.ac.uk/efo/EFO_0010749 GCST012137 Genome-wide genotyping array 2021-11-15 34202464 Wang M 2021-06-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34202464 Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ABO blood group (O vs non-O) up to 356 Han Chinese ancestry individuals with O blood group, up to 622 Han Chinese ancestry individuals with non-O blood group NA Affymetrix [733907] 2 blood group O http://www.ebi.ac.uk/efo/EFO_0600063 GCST012522 Genome-wide genotyping array 2021-11-15 34202464 Wang M 2021-06-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34202464 Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ABO blood group (A vs non-A) up to 322 Han Chinese ancestry individuals with A blood group, up to 686 Han Chinese ancestry individuals with non-A blood group NA Affymetrix [733907] 2 blood group A http://www.ebi.ac.uk/efo/EFO_0600060 GCST012521 Genome-wide genotyping array 2021-11-15 34202464 Wang M 2021-06-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34202464 Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ABO blood group (B vs non-B) up to 253 Han Chinese ancestry individuals with B blood group, up to 755 Han Chinese ancestry individuals with non-B blood group NA Affymetrix [733907] 2 blood group B http://www.ebi.ac.uk/efo/EFO_0600061 GCST012520 Genome-wide genotyping array 2021-11-15 34202464 Wang M 2021-06-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34202464 Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ABO blood group (AB vs non-AB) up to 77 Han Chinese ancestry individuals with AB blood group, up to 931 Han Chinese ancestry individuals with non-AB blood group NA Affymetrix [733907] 2 blood group AB http://www.ebi.ac.uk/efo/EFO_0600062 GCST012519 Genome-wide genotyping array 2021-11-15 34202464 Wang M 2021-06-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34202464 Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ABO blood group (A vs O) up to 322 Han Chinese ancestry individuals with A blood group, up to 356 Han Chinese ancestry individuals with A blood group NA Affymetrix [733907] 2 blood group O, blood group A http://www.ebi.ac.uk/efo/EFO_0600063, http://www.ebi.ac.uk/efo/EFO_0600060 GCST012518 Genome-wide genotyping array 2021-11-15 34202464 Wang M 2021-06-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34202464 Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ABO blood group (B vs O) up to 235 Han Chinese ancestry individuals with B blood group, up to 356 Han Chinese ancestry individuals with O blood group NA Affymetrix [733907] 2 blood group B, blood group O http://www.ebi.ac.uk/efo/EFO_0600061, http://www.ebi.ac.uk/efo/EFO_0600063 GCST012517 Genome-wide genotyping array 2021-11-15 34202464 Wang M 2021-06-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34202464 Genomic Association vs. Serological Determination of ABO Blood Types in a Chinese Cohort, with Application in Mendelian Randomization. ABO blood group (AB vs O) up to 77 Han Chinese ancestry individuals with AB blood group, up to 356 individuals with O blood group NA Affymetrix [733907] 2 blood group AB, blood group O http://www.ebi.ac.uk/efo/EFO_0600062, http://www.ebi.ac.uk/efo/EFO_0600063 GCST012516 Genome-wide genotyping array 2021-10-05 33979311 Yanik EL 2021-05-12 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/33979311 Identification of a Novel Genetic Marker for Risk of Degenerative Rotator Cuff Disease Surgery in the UK Biobank. Degenerative rotator cuff disease surgery 2,917 British ancestry cases, 14,158 British ancestry controls NA Affymetrix [10815322] (imputed) 1 rotator cuff tear http://www.ebi.ac.uk/efo/EFO_1001250 GCST90020231 Genome-wide genotyping array 2021-09-29 33904754 Cartwright R 2021-04-27 J Urol www.ncbi.nlm.nih.gov/pubmed/33904754 Genome Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence. Urinary incontinence 2,942 European ancestry cases, 6,037 European ancestry controls 2,065 European ancestry cases, 2,004 European ancestry controls Illumina [9700000] (imputed) 2 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90025928 Genome-wide genotyping array 2021-09-29 33904754 Cartwright R 2021-04-27 J Urol www.ncbi.nlm.nih.gov/pubmed/33904754 Genome Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence. Stress urinary incontinence 2,072 European ancestry cases, 6,907 European ancestry controls 1,321 European ancestry cases, 2,748 European ancestry controls Illumina [9700000] (imputed) 2 Stress urinary incontinence http://purl.obolibrary.org/obo/HP_0010992 GCST90025929 Genome-wide genotyping array 2021-09-29 33904754 Cartwright R 2021-04-27 J Urol www.ncbi.nlm.nih.gov/pubmed/33904754 Genome Wide Association Study Identifies Two Novel Loci Associated with Female Stress and Urgency Urinary Incontinence. Urgency urinary incontinence 870 European ancestry cases, 8,109 European ancestry controls 744 European ancestry cases, 3,325 European ancestry controls Illumina [9700000] (imputed) 2 urgency urinary incontinence http://www.ebi.ac.uk/efo/EFO_0006865 GCST90025930 Genome-wide genotyping array 2021-10-08 34548389 Yu Z 2021-09-21 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/34548389 Polygenic Risk Scores for Kidney Function and Their Associations with Circulating Proteome, and Incident Kidney Diseases. Estimated glomerular filtration rate (creatinine) 949,116 European ancestry individuals, 166,997 East Asian ancestry individuals, 21,338 South Asian ancestry individuals, 17,459 African American individuals, 4,961 Hispanic individuals NA Affymetrix, Illumina [8439544] (imputed) 0 creatinine measurement, glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0004518, http://www.ebi.ac.uk/efo/EFO_0005208 GCST90026654 Genome-wide genotyping array 2021-10-22 34212547 An J 2021-07-01 Allergy Asthma Immunol Res www.ncbi.nlm.nih.gov/pubmed/34212547 Genome-Wide Association Study of Korean Asthmatics: A Comparison With UK Asthmatics. Adult asthma 1,386 Korean ancestry cases, 5,205 Korean ancestry controls NA Affymetrix [4922160] (imputed) 10 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90025849 Genome-wide genotyping array 2021-10-15 34560606 Park S 2021-09-09 Clin Nutr www.ncbi.nlm.nih.gov/pubmed/34560606 Association between polygenetic risk scores related to sarcopenia risk and their interactions with regular exercise in a large cohort of Korean adults. sarcopenia 1,368 Korean ancestry cases, 15,742 Korean ancestry controls NA Affymetrix [NR] 2 sarcopenia http://www.ebi.ac.uk/efo/EFO_1000653 GCST90044764 Genome-wide genotyping array 2021-10-29 34356046 Oluwafemi OO 2021-07-01 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34356046 Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Conotruncal heart defects with normally related great vessels in 22q.11.2 deletion syndrome 913 cases, 559 controls NA Affymetrix [3311160] (imputed) 5 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST90026409 Genome-wide genotyping array 2021-10-29 34356046 Oluwafemi OO 2021-07-01 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34356046 Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Conotruncal heart defects with normally related great vessels (without 22q.11.2 deletion syndrome) 294 European ancestry cases, 2,976 European ancestry controls, 641 trios NA Illumina [3311160] (imputed) 25 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST90026410 Genome-wide genotyping array 2021-10-29 34356046 Oluwafemi OO 2021-07-01 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/34356046 Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Conotruncal heart defects with normally related great vessels 294 European ancestry cases, 2,976 European ancestry controls, 913 cases, 559 controls, 641 trios NA Affymetrix, Illumina [3311160] (imputed) 16 conotruncal heart malformations http://purl.obolibrary.org/obo/MONDO_0016581 GCST90026411 Genome-wide genotyping array 2021-07-29 34262104 Meijer AJM 2021-07-14 NPJ Precis Oncol www.ncbi.nlm.nih.gov/pubmed/34262104 TCERG1L allelic variation is associated with cisplatin-induced hearing loss in childhood cancer, a PanCareLIFE study. Cisplatin-induced hearing loss in childhood cancer 168 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American child cases, 222 European, African American or Afro-Caribbean, Hispanic or Latin American ancestry child controls 209 child cases, 171 child controls Illumina [673489] (imputed) 1 ototoxicity, hearing loss, response to cisplatin http://www.ebi.ac.uk/efo/EFO_0006951, http://www.ebi.ac.uk/efo/EFO_0004238, http://purl.obolibrary.org/obo/GO_0072718 GCST90013831 Genome-wide genotyping array 2022-03-22 34868232 Feng S 2021-11-18 Front Genet www.ncbi.nlm.nih.gov/pubmed/34868232 Regulatory SNP of RREB1 is Associated With Bone Mineral Density in Chinese Postmenopausal Osteoporosis Patients. Bone mineral density T score in postmenopausal osteoporosis 150 Han Chinese ancestry individuals 191 Han Chinese ancestry individuals Illumina [311319] 1 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90096797 Genome-wide genotyping array 2022-03-28 34590679 Pott J 2021-09-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34590679 Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2. PCSK9 levels 12,721 European ancestry individuals NA Affymetrix, Illumina [8700000] (imputed) 18 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90096812 Genome-wide genotyping array 2022-03-28 34590679 Pott J 2021-09-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34590679 Meta-GWAS of PCSK9 levels detects two novel loci at APOB and TM6SF2. PCSK9 levels 10,186 European ancestry statin-free individuals 300 African American statin-free individuals Affymetrix, Illumina [8700000] (imputed) 21 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90096813 Genome-wide genotyping array 2021-08-13 34308111 Amin HA 2021-01-07 BMJ Nutr Prev Health www.ncbi.nlm.nih.gov/pubmed/34308111 No evidence that vitamin D is able to prevent or affect the severity of COVID-19 in individuals with European ancestry: a Mendelian randomisation study of open data. Vitamin D insufficiency 35,079 European ancestry cases, 140,898 European ancestry controls NA Affymetrix [812428] 17 vitamin D deficiency http://www.ebi.ac.uk/efo/EFO_0003762 GCST90020244 Genome-wide genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation-estimated granulocyte proportions 34,470 European ancestry individuals NA Affymetrix, Illumina [7568298] (imputed) 2 granulocyte count http://www.ebi.ac.uk/efo/EFO_0007987 GCST90014287 Genome-wide genotyping array, Genome-wide sequencing, Exome genotyping array, Targeted genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation GrimAge acceleration 34,467 European ancestry individuals NA Affymetrix, Illumina [7568149] (imputed) 4 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014288 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation Hannum age acceleration 34,449 European ancestry individuals NA Affymetrix, Illumina [7565493] (imputed) 9 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014289 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. Intrinsic epigenetic age acceleration 34,461 European ancestry individuals NA Affymetrix, Illumina [7567980] (imputed) 24 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014290 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation-estimated plasminogen activator inhibitor-1 levels 34,448 European ancestry individuals NA Affymetrix, Illumina [7567618] (imputed) 5 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90014291 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation PhenoAge acceleration 34,463 European ancestry individuals NA Affymetrix, Illumina [7568033] (imputed) 12 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014292 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation-estimated granulocyte proportions 6,152 African American individuals NA Affymetrix, Illumina [12990599] (imputed) 27 granulocyte count http://www.ebi.ac.uk/efo/EFO_0007987 GCST90014293 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation GrimAge acceleration 6,148 African American individuals NA Affymetrix, Illumina [12989440] (imputed) 11 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014294 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation Hannum age acceleration 6,148 African American individuals NA Affymetrix, Illumina [12989706] (imputed) 11 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014295 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. Intrinsic epigenetic age acceleration 6,148 African American individuals NA Affymetrix, Illumina [12989965] (imputed) 9 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014296 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation-estimated plasminogen activator inhibitor-1 levels 6,149 African American individuals NA Affymetrix, Illumina [12990252] (imputed) 11 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90014297 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation PhenoAge acceleration 6,148 African American individuals NA Affymetrix, Illumina [12989038] (imputed) 12 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014298 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation-estimated granulocyte proportions 34,470 European ancestry individuals, 6,152 African American individuals NA Affymetrix, Illumina [6210527] (imputed) 8 granulocyte count http://www.ebi.ac.uk/efo/EFO_0007987 GCST90014299 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation GrimAge acceleration 34,467 European ancestry individuals, 6,148 African American individuals NA Affymetrix, Illumina [6210740] (imputed) 6 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014300 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation Hannum age acceleration 34,449 European ancestry individuals, 6,148 African American individuals NA Affymetrix, Illumina [6210504] (imputed) 10 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014301 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. Intrinsic epigenetic age acceleration 34,461 European ancestry individuals, 6,148 African American individuals NA Affymetrix, Illumina [6211246] (imputed) 22 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014302 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation-estimated plasminogen activator inhibitor-1 levels 34,448 European ancestry individuals, 6,149 African American individuals NA Affymetrix, Illumina [6211016] (imputed) 10 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90014303 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-07-27 34187551 McCartney DL 2021-06-29 Genome Biol www.ncbi.nlm.nih.gov/pubmed/34187551 Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging. DNA methylation PhenoAge acceleration 34,463 European ancestry individuals, 6,148 African American individuals NA Affymetrix, Illumina [6210360] (imputed) 10 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90014304 Genome-wide genotyping array, Targeted genotyping array, Exome genotyping array, Genome-wide sequencing 2021-10-15 34337005 Duan H 2021-07-17 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/34337005 A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins. Hearing function (0.5 kHz) 131 Chinese ancestry dizygotic twin pairs NA Illumina [1365315] 7 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST90027021 Genome-wide genotyping array 2021-10-15 34337005 Duan H 2021-07-17 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/34337005 A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins. Hearing function (1 kHz) 131 Chinese ancestry dizygotic twin pairs NA Illumina [1365315] 5 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST90027022 Genome-wide genotyping array 2021-10-15 34337005 Duan H 2021-07-17 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/34337005 A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins. Hearing function (2 kHz) 131 Chinese ancestry dizygotic twin pairs NA Illumina [1365315] 14 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST90027023 Genome-wide genotyping array 2021-10-15 34337005 Duan H 2021-07-17 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/34337005 A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins. Hearing function (4 kHz) 131 Chinese ancestry dizygotic twin pairs NA Illumina [1365315] 5 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST90027024 Genome-wide genotyping array 2021-10-15 34337005 Duan H 2021-07-17 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/34337005 A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins. Hearing function (8 kHz) 131 Chinese ancestry dizygotic twin pairs NA Illumina [1365315] 9 hearing threshold measurement, hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007616 GCST90027025 Genome-wide genotyping array 2021-10-15 34337005 Duan H 2021-07-17 Biomed Res Int www.ncbi.nlm.nih.gov/pubmed/34337005 A Genome-Wide Association Study of Age-Related Hearing Impairment in Middle- and Old-Aged Chinese Twins. Hearing function 131 Chinese ancestry dizygotic twin pairs NA Illumina [1365315] 4 hearing threshold measurement, pure tone hearing measurement http://www.ebi.ac.uk/efo/EFO_0007618, http://www.ebi.ac.uk/efo/EFO_0007617 GCST90027026 Genome-wide genotyping array 2021-11-12 33889958 Gurung RL 2021-04-23 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/33889958 Association of genetic variants for plasma LRG1 with rapid decline in kidney function in patients with type 2 diabetes. Leucine-rich alpha-2-glycoprotein 1 levels in type 2 diabetes 983 Chinese ancestry individuals, 420 Malay ancestry individuals, 478 Indian ancestry individuals 1,813 Chinese ancestry individuals Illumina [705416] 1 plasma leucine rich alpha-2-glycoprotein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600050 GCST90020073 Genome-wide genotyping array 2021-09-09 34159637 Otomo N 2021-06-22 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/34159637 Polygenic Risk Score of Adolescent Idiopathic Scoliosis for Potential Clinical Use. Adolescent idiopathic scoliosis (Cobb angle) 4,465 Japanese ancestry individuals NA NR [NR] 0 adolescent idiopathic scoliosis http://www.ebi.ac.uk/efo/EFO_0005423 GCST012369 Genome-wide genotyping array 2021-11-02 34224794 Wang K 2021-07-02 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34224794 Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes. Perceptual and visual search speed (trail making test A) 684 European ancestry individuals, 17 Hispanic individuals, 36 African American individuals, 18 individuals NA NR [534934] 5 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST90025850 Genome-wide genotyping array 2021-11-02 34224794 Wang K 2021-07-02 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34224794 Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes. Executive function (trail making test B) 684 European ancestry individuals, 17 Hispanic individuals, 36 African American individuals, 18 individuals NA NR [534934] 3 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90025851 Genome-wide genotyping array 2021-11-02 34224794 Wang K 2021-07-02 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34224794 Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes. Disability level (impaired activities of daily living) 684 European ancestry individuals, 17 Hispanic individuals, 36 African American individuals, 18 individuals NA NR [534934] 12 activities of daily living score measurement http://www.ebi.ac.uk/efo/EFO_0008451 GCST90025852 Genome-wide genotyping array 2021-11-02 34224794 Wang K 2021-07-02 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34224794 Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) 684 European ancestry individuals, 17 Hispanic individuals, 36 African American individuals, 18 individuals NA NR [534934] 8 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90025853 Genome-wide genotyping array 2021-11-02 34224794 Wang K 2021-07-02 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34224794 Genome-wide association study identified INSC gene associated with Trail Making Test Part A and Alzheimer's disease related cognitive phenotypes. Cognitive impairment level 684 European ancestry individuals, 17 Hispanic individuals, 36 African American individuals, 18 individuals NA NR [534934] 7 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90025854 Genome-wide genotyping array 2021-10-19 34075027 Gonda X 2021-06-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34075027 Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. Anxious temperament 775 European ancestry individuals NA Illumina [2550710] (imputed) 6 TEMPS-A questionnaire http://www.ebi.ac.uk/efo/EFO_0004783 GCST90020036 Genome-wide genotyping array 2021-10-19 34075027 Gonda X 2021-06-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34075027 Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. Cyclothymic temperament 775 European ancestry individuals NA Illumina [2550710] (imputed) 5 TEMPS-A questionnaire http://www.ebi.ac.uk/efo/EFO_0004783 GCST90020037 Genome-wide genotyping array 2021-10-19 34075027 Gonda X 2021-06-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34075027 Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. Depressive temperament 775 European ancestry individuals NA Illumina [2550710] (imputed) 3 TEMPS-A questionnaire http://www.ebi.ac.uk/efo/EFO_0004783 GCST90020038 Genome-wide genotyping array 2021-10-19 34075027 Gonda X 2021-06-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34075027 Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. Irritable temperament 775 European ancestry individuals NA Illumina [2550710] (imputed) 2 TEMPS-A questionnaire http://www.ebi.ac.uk/efo/EFO_0004783 GCST90020039 Genome-wide genotyping array 2021-10-19 34075027 Gonda X 2021-06-01 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34075027 Genetic underpinnings of affective temperaments: a pilot GWAS investigation identifies a new genome-wide significant SNP for anxious temperament in ADGRB3 gene. Hyperthymic temperament 775 European ancestry individuals NA Illumina [2550710] (imputed) 4 TEMPS-A questionnaire http://www.ebi.ac.uk/efo/EFO_0004783 GCST90020040 Genome-wide genotyping array 2022-11-24 34442380 Hernandez-Pacheco N 2021-07-28 J Pers Med www.ncbi.nlm.nih.gov/pubmed/34442380 Identification of ROBO2 as a Potential Locus Associated with Inhaled Corticosteroid Response in Childhood Asthma. Response to inhaled corticosteroid treatment in asthma (change in FEV1) 94 Slovenian ancestry cases, 72 Slovenian ancestry controls 93 European ancestry cases, 80 European ancestry controls Illumina [7500000] (imputed) 0 FEV change measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0005921, http://purl.obolibrary.org/obo/GO_0031960 GCST90027445 Genome-wide genotyping array 2021-07-07 34050200 Choi JW 2021-05-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34050200 Genetically determined hypoalbuminemia as a risk factor for hypertension: instrumental variable analysis. Hypoalbuminemia 1,168 East Asian ancestry cases, 3,157 East Asian ancestry controls NA Affymetrix [519364] 4 Hypoalbuminemia http://purl.obolibrary.org/obo/HP_0003073 GCST012007 Genome-wide genotyping array 2021-10-11 34184781 O'Connor E 2021-06-29 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/34184781 Genome Wide Association Study Identifies Risk Loci For Cluster Headache. Cluster headache 1,443 European ancestry cases, 6,748 European ancestry controls NA Illumina [NR] (imputed) 4 Cluster headache http://purl.obolibrary.org/obo/HP_0012199 GCST012478 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Peripheral Neuropathy) 707 European ancestry individuals NA NR [4178855] (imputed) 0 peripheral neuropathy, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017191 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Peripheral Neuropathy) 348 European ancestry individuals NA NR [4176489] (imputed) 0 peripheral neuropathy, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017192 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Peripheral Neuropathy) 385 European ancestry individuals NA NR [4176743] (imputed) 0 peripheral neuropathy, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017193 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Peripheral Neuropathy) 360 European ancestry individuals NA NR [4164603] (imputed) 0 peripheral neuropathy, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017194 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Stomatitis) 707 European ancestry individuals NA NR [4167969] (imputed) 0 chemotherapy-induced cytotoxicity measurement, stomatitis http://www.ebi.ac.uk/efo/EFO_0010978, http://www.ebi.ac.uk/efo/EFO_0009688 GCST90017195 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Stomatitis) 348 European ancestry individuals NA NR [4161930] (imputed) 0 chemotherapy-induced cytotoxicity measurement, stomatitis http://www.ebi.ac.uk/efo/EFO_0010978, http://www.ebi.ac.uk/efo/EFO_0009688 GCST90017196 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Stomatitis) 385 European ancestry individuals NA NR [4177511] (imputed) 0 chemotherapy-induced cytotoxicity measurement, stomatitis http://www.ebi.ac.uk/efo/EFO_0010978, http://www.ebi.ac.uk/efo/EFO_0009688 GCST90017197 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Stomatitis) 360 European ancestry individuals NA NR [4178858] (imputed) 0 chemotherapy-induced cytotoxicity measurement, stomatitis http://www.ebi.ac.uk/efo/EFO_0010978, http://www.ebi.ac.uk/efo/EFO_0009688 GCST90017198 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Nausea) 707 European ancestry individuals NA NR [4178858] (imputed) 0 chemotherapy-induced cytotoxicity measurement, Nausea http://www.ebi.ac.uk/efo/EFO_0010978, http://purl.obolibrary.org/obo/HP_0002018 GCST90017199 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Nausea) 348 European ancestry individuals NA NR [4178713] (imputed) 0 chemotherapy-induced cytotoxicity measurement, Nausea http://www.ebi.ac.uk/efo/EFO_0010978, http://purl.obolibrary.org/obo/HP_0002018 GCST90017200 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Nausea) 385 European ancestry individuals NA NR [4175233] (imputed) 0 chemotherapy-induced cytotoxicity measurement, Nausea http://www.ebi.ac.uk/efo/EFO_0010978, http://purl.obolibrary.org/obo/HP_0002018 GCST90017201 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Nausea) 360 European ancestry individuals NA NR [4176780] (imputed) 1 chemotherapy-induced cytotoxicity measurement, Nausea http://www.ebi.ac.uk/efo/EFO_0010978, http://purl.obolibrary.org/obo/HP_0002018 GCST90017202 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Vomiting) 707 European ancestry individuals NA NR [4178857] (imputed) 0 Vomiting, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002013, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017203 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Vomiting) 348 European ancestry individuals NA NR [4171342] (imputed) 0 Vomiting, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002013, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017204 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Vomiting) 385 European ancestry individuals NA NR [4150631] (imputed) 0 Vomiting, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002013, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017205 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Vomiting) 360 European ancestry individuals NA NR [4169348] (imputed) 0 Vomiting, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002013, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017206 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Diarrhoea) 707 European ancestry individuals NA NR [4178858] (imputed) 0 Diarrhea, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002014, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017207 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Diarrhoea) 348 European ancestry individuals NA NR [4178858] (imputed) 1 Diarrhea, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002014, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017208 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Diarrhoea) 385 European ancestry individuals NA NR [4178775] (imputed) 0 Diarrhea, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002014, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017209 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Diarrhoea) 360 European ancestry individuals NA NR [4178855] (imputed) 0 Diarrhea, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/HP_0002014, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017210 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Lethargy) 707 European ancestry individuals NA NR [4178858] (imputed) 1 sleepiness, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/NCIT_C95746, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017211 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Lethargy) 348 European ancestry individuals NA NR [4178857] (imputed) 0 sleepiness, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/NCIT_C95746, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017212 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Lethargy) 385 European ancestry individuals NA NR [4178858] (imputed) 0 sleepiness, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/NCIT_C95746, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017213 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Lethargy) 360 European ancestry individuals NA NR [4178858] (imputed) 0 sleepiness, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/NCIT_C95746, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017214 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Neutropenia) 707 European ancestry individuals NA NR [4172253] (imputed) 0 neutropenia, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/MONDO_0001475, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017215 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Neutropenia) 348 European ancestry individuals NA NR [3560566] (imputed) 0 neutropenia, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/MONDO_0001475, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017216 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Neutropenia) 385 European ancestry individuals NA NR [4178853] (imputed) 0 neutropenia, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/MONDO_0001475, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017217 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Neutropenia) 360 European ancestry individuals NA NR [4178858] (imputed) 1 neutropenia, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/MONDO_0001475, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017218 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Hand foot syndrome) 707 European ancestry individuals NA NR [4178084] (imputed) 0 Hand-foot syndrome, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_1001893, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017219 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) (Hand foot syndrome) 348 European ancestry individuals NA NR [4178292] (imputed) 0 Hand-foot syndrome, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_1001893, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017220 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Hand foot syndrome) 385 European ancestry individuals NA NR [3841701] (imputed) 1 Hand-foot syndrome, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_1001893, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017221 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Hand foot syndrome) 360 European ancestry individuals NA NR [4178072] (imputed) 0 Hand-foot syndrome, chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_1001893, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017222 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) 707 European ancestry individuals NA NR [4986536] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017223 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX,Cetuximab) 348 European ancestry individuals NA NR [4986536] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017224 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) 385 European ancestry individuals NA NR [4986536] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017225 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX, Cetuximab) 360 European ancestry individuals NA NR [4986536] (imputed) 0 chemotherapy-induced cytotoxicity measurement http://www.ebi.ac.uk/efo/EFO_0010978 GCST90017226 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX) (Sepsis) 385 European ancestry individuals NA NR [4145880] (imputed) 0 chemotherapy-induced cytotoxicity measurement, Sepsis http://www.ebi.ac.uk/efo/EFO_0010978, http://purl.obolibrary.org/obo/HP_0100806 GCST90017227 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Sepsis) 360 European ancestry individuals NA NR [4174431] (imputed) 0 chemotherapy-induced cytotoxicity measurement, Sepsis http://www.ebi.ac.uk/efo/EFO_0010978, http://purl.obolibrary.org/obo/HP_0100806 GCST90017228 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX) (Rash) 707 European ancestry individuals NA NR [3948970] (imputed) 0 chemotherapy-induced cytotoxicity measurement, exanthem http://www.ebi.ac.uk/efo/EFO_0010978, http://www.ebi.ac.uk/efo/EFO_1000697 GCST90017229 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (XELOX, Cetuximab) (Rash) 348 European ancestry individuals NA NR [4178858] (imputed) 0 chemotherapy-induced cytotoxicity measurement, exanthem http://www.ebi.ac.uk/efo/EFO_0010978, http://www.ebi.ac.uk/efo/EFO_1000697 GCST90017230 Genome-wide genotyping array 2021-07-27 34270794 Watts K 2021-07-16 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/34270794 Genome-wide association studies of toxicity to oxaliplatin and fluoropyrimidine chemotherapy with or without cetuximab in 1800 patients with advanced colorectal cancer. Adverse response to chemotherapy in colorectal cancer (FOLFOX,Cetuximab) (Rash) 360 European ancestry individuals NA NR [4178858] (imputed) 0 chemotherapy-induced cytotoxicity measurement, exanthem http://www.ebi.ac.uk/efo/EFO_0010978, http://www.ebi.ac.uk/efo/EFO_1000697 GCST90017231 Genome-wide genotyping array 2021-09-03 34338756 Ahlberg G 2021-07-29 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/34338756 Genome-wide association study identifies 18 novel loci associated with left atrial volume and function. Left atrial maximum volume 35,658 British ancestry individuals NA Affymetrix [10600000] (imputed) 2 left atrial volume measurement http://www.ebi.ac.uk/efo/EFO_0600035 GCST90025936 Genome-wide genotyping array 2021-09-03 34338756 Ahlberg G 2021-07-29 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/34338756 Genome-wide association study identifies 18 novel loci associated with left atrial volume and function. Left atrial minimum volume 35,658 British ancestry individuals NA Affymetrix [10600000] (imputed) 3 left atrial volume measurement http://www.ebi.ac.uk/efo/EFO_0600035 GCST90025937 Genome-wide genotyping array 2021-09-03 34338756 Ahlberg G 2021-07-29 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/34338756 Genome-wide association study identifies 18 novel loci associated with left atrial volume and function. Left atrial active emptying fraction 35,658 British ancestry individuals NA Affymetrix [10600000] (imputed) 6 left atrial function http://www.ebi.ac.uk/efo/EFO_0004294 GCST90025938 Genome-wide genotyping array 2021-09-03 34338756 Ahlberg G 2021-07-29 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/34338756 Genome-wide association study identifies 18 novel loci associated with left atrial volume and function. Left atrial passive emptying fraction 35,658 British ancestry individuals NA Affymetrix [10600000] (imputed) 2 left atrial function http://www.ebi.ac.uk/efo/EFO_0004294 GCST90025939 Genome-wide genotyping array 2021-09-03 34338756 Ahlberg G 2021-07-29 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/34338756 Genome-wide association study identifies 18 novel loci associated with left atrial volume and function. Left atrial total emptying fraction 35,658 British ancestry individuals NA Affymetrix [10600000] (imputed) 5 left atrial function http://www.ebi.ac.uk/efo/EFO_0004294 GCST90025940 Genome-wide genotyping array 2021-09-29 34031191 Kumar A 2021-05-24 Neurology www.ncbi.nlm.nih.gov/pubmed/34031191 Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India. Stroke 1,255 Indian ancestry cases, 2,154 Indian ancestry controls 211 South Asian ancestry cases, 7,417 South Asian ancestry controls Illumina [7827597] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90020238 Genome-wide genotyping array 2021-09-29 34031191 Kumar A 2021-05-24 Neurology www.ncbi.nlm.nih.gov/pubmed/34031191 Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India. Stroke (ischemic) 1,077 Indian ancestry cases, 2,154 Indian ancestry controls 98 South Asian ancestry cases, 7,421 South Asian ancestry controls Illumina [up to 7827597] (imputed) 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90020239 Genome-wide genotyping array 2021-09-29 34031191 Kumar A 2021-05-24 Neurology www.ncbi.nlm.nih.gov/pubmed/34031191 Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India. Large artery stroke 350 Indian ancestry cases, 2,154 Indian ancestry controls NA Illumina [up to 7827597] (imputed) 31 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90020240 Genome-wide genotyping array 2021-09-29 34031191 Kumar A 2021-05-24 Neurology www.ncbi.nlm.nih.gov/pubmed/34031191 Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India. Small vessel stroke 333 Indian ancestry cases, 2,154 Indian ancestry controls NA Illumina [7827597] (imputed) 43 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90020241 Genome-wide genotyping array 2021-09-29 34031191 Kumar A 2021-05-24 Neurology www.ncbi.nlm.nih.gov/pubmed/34031191 Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India. Ischemic stroke (cardioembolic) 174 Indian ancestry cases, 2,154 Indian ancestry controls NA Illumina [up to 7827597] (imputed) 61 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90020242 Genome-wide genotyping array 2021-09-29 34031191 Kumar A 2021-05-24 Neurology www.ncbi.nlm.nih.gov/pubmed/34031191 Association of SUMOlation Pathway Genes With Stroke in a Genome-wide Association Study in India. Stroke (hemorhagic) 178 Indian ancestry cases, 2,154 Indian ancestry controls 25 South Asian ancestry cases, 7,424 South Asian ancestry controls Illumina [up to 7827597] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90020243 Genome-wide genotyping array 2021-09-06 33783510 Fatumo S 2021-03-30 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33783510 Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Estimated glomerular filtration rate 3,288 Ugandan ancestry individuals 8,224 African American individuals Illumina [20594556] (imputed) 4 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90025873 Genome-wide genotyping array, Genome-wide sequencing 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Alanine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90104955 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Glutamine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90104956 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Glycine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90104957 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Histidine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90104958 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Isoleucine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90104959 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Leucine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90104960 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Phenylalanine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90104961 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Tyrosine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90104962 Genome-wide genotyping array 2022-07-01 29481666 Teslovich TM 2018-05-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29481666 Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study. Valine levels 8,545 Finnish ancestry males 2,591 Finnish ancestry individuals Illumina [16607533] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90104963 Genome-wide genotyping array 2021-11-19 34242216 Ray D 2021-07-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34242216 Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. Cleft lip with or without cleft palate or cleft palate (pleiotropy) 300 Asian ancestry cleft lip trios, 299 European ancestry cleft lip trios, 89 Latin American cleft lip trios, 6 cleft lip trios, 875 Asian ancestry cleft lip with cleft palate trios, 679 European ancestry cleft lip with cleft palate trios, 508 Latin American cleft lip with cleft palate trios, 15 cleft lip with cleft palate trios, 273 Asian ancestry cleft palate trios, 296 European ancestry cleft palate trios, 28 Latin American cleft palate trios, 14 cleft palate trios NA Illumina [6761961] (imputed) 9 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST90026473 Genome-wide genotyping array 2021-11-19 34242216 Ray D 2021-07-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34242216 Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. Cleft lip or cleft palate (pleiotropy) 300 Asian ancestry cleft lip trios, 299 European ancestry cleft lip trios, 89 Latin American cleft lip trios, 6 cleft lip trios, 273 Asian ancestry cleft palate trios, 296 European ancestry cleft palate trios, 28 Latin American cleft palate trios, 14 cleft palate trios NA Illumina [6761961] (imputed) 1 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST90026474 Genome-wide genotyping array 2021-11-19 34242216 Ray D 2021-07-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34242216 Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. Cleft lip with cleft palate or cleft palate (pleiotropy) 875 Asian ancestry cleft lip with cleft palate trios, 679 European ancestry cleft lip with cleft palate trios, 508 Latin American cleft lip with cleft palate trios, 15 cleft lip with cleft palate trios, 273 Asian ancestry cleft palate trios, 296 European ancestry cleft palate trios, 28 Latin American cleft palate trios, 14 cleft palate trios NA Illumina [6761961] (imputed) 1 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST90026475 Genome-wide genotyping array 2021-11-19 34242216 Ray D 2021-07-09 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34242216 Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios. Cleft lip or cleft lip with cleft palate (pleiotropy) 300 Asian ancestry cleft lip trios, 299 European ancestry cleft lip trios, 89 Latin American cleft lip trios, 6 cleft lip trios, 875 Asian ancestry cleft lip with cleft palate trios, 679 European ancestry cleft lip with cleft palate trios, 508 Latin American cleft lip with cleft palate trios, 15 cleft lip with cleft palate trios NA Illumina [6761961] (imputed) 1 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST90026476 Genome-wide genotyping array 2022-06-20 35304435 Jamshidi J 2022-03-19 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35304435 Phenotypic and genetic analysis of a wellbeing factor score in the UK Biobank and the impact of childhood maltreatment and psychiatric illness. Wellbeing index 129,237 British ancestry individuals NA Affymetrix [8068119] (imputed) 5 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90104627 Genome-wide genotyping array 2022-06-20 35304435 Jamshidi J 2022-03-19 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35304435 Phenotypic and genetic analysis of a wellbeing factor score in the UK Biobank and the impact of childhood maltreatment and psychiatric illness. Childhood maltreatment 45,723 British ancestry individuals NA Affymetrix [8068119] (imputed) 3 childhood trauma measurement http://www.ebi.ac.uk/efo/EFO_0007979 GCST90104628 Genome-wide genotyping array 2022-01-06 34902334 Trepo E 2021-12-11 Lancet Oncol www.ncbi.nlm.nih.gov/pubmed/34902334 Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study. Alcohol-related hepatocellular carcinoma 775 European ancestry cases, 1,332 European ancestry controls NA Illumina [7962325] (imputed) 3 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90092003 Genome-wide genotyping array 2022-01-27 34026292 Juang JJ 2020-12-07 J Adv Res www.ncbi.nlm.nih.gov/pubmed/34026292 Rare variants discovery by extensive whole-genome sequencing of the Han Chinese population in Taiwan: Applications to cardiovascular medicine. Hypertension 2,936 Han Chinese ancestry cases, 7,742 Han Chinese ancestry controls NA NR [577656] 8 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90086157 Genome-wide genotyping array 2021-07-27 34101054 Nikopensius T 2021-06-08 Clin Rheumatol www.ncbi.nlm.nih.gov/pubmed/34101054 Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients. Arthritis (juvenile idiopathic) 263 Estonian ancestry cases, 6,956 Estonian ancestry controls NA Illumina [16583468] (imputed) 2 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST012103 Genome-wide genotyping array 2021-07-27 34101054 Nikopensius T 2021-06-08 Clin Rheumatol www.ncbi.nlm.nih.gov/pubmed/34101054 Association analysis of juvenile idiopathic arthritis genetic susceptibility factors in Estonian patients. Arthritis (oligoarticular juvenile idiopathic) Up to 263 Estonian ancestry cases, up to 6,956 Estonian ancestry controls NA Illumina [up to 16583468] (imputed) 1 oligoarticular juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_1002019 GCST012102 Genome-wide genotyping array 2022-01-06 34542150 Gergei I 2021-09-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34542150 GWAS META-analysis followed by MENDELIAN randomisation revealed potential control mechanisms for circulating α-klotho levels. Circulating plasma alpha-Klotho levels 4,376 European ancestry individuals NA Affymetrix, Illumina [6439450] (imputed) 6 circulating alpha-Klotho measurement http://www.ebi.ac.uk/efo/EFO_0020102 GCST90091246 Genome-wide genotyping array 2022-01-06 34542150 Gergei I 2021-09-20 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34542150 GWAS META-analysis followed by MENDELIAN randomisation revealed potential control mechanisms for circulating α-klotho levels. Circulating plasma alpha-Klotho levels 4,675 European ancestry individuals NA Affymetrix, Illumina [6439450] (imputed) 0 circulating alpha-Klotho measurement http://www.ebi.ac.uk/efo/EFO_0020102 GCST90091247 Genome-wide genotyping array 2021-07-15 31819081 Rivera NV 2019-12-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31819081 A Gene-Environment Interaction Between Smoking and Gene polymorphisms Provides a High Risk of Two Subgroups of Sarcoidosis. Sarcoidosis (non-Lofgren's syndrome) (smoking status interaction) 230 European ancestry never smoker cases, 225 European ancestry ever smoker cases, 1,349 European ancestry never smoker controls, 1,617 European ancestry ever smoker controls NA Illumina [186000] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST012029 Targeted genotyping array [ImmunoChip] 2021-07-15 31819081 Rivera NV 2019-12-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31819081 A Gene-Environment Interaction Between Smoking and Gene polymorphisms Provides a High Risk of Two Subgroups of Sarcoidosis. Sarcoidosis (Lofgren's syndrome) (smoking status interaction) 155 European ancestry never smoker cases, 137 European ancestry ever smoker cases, 1,349 European ancestry never smoker controls, 1,617 European ancestry ever smoker controls NA Illumina [186000] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST012030 Targeted genotyping array [ImmunoChip] 2022-06-20 35366586 Kim J 2022-03-07 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/35366586 Ethnic differences in the frequency of β-amyloid deposition in cognitively normal individuals. Amyloid beta positivity in normal cognition 175 Korean ancestry individuals 69 Korean ancestry individuals Illumina [4906407] (imputed) 2 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90104611 Genome-wide genotyping array 2022-06-20 35366586 Kim J 2022-03-07 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/35366586 Ethnic differences in the frequency of β-amyloid deposition in cognitively normal individuals. Amyloid beta positivity in normal cognition 196 European ancestry individuals NA Illumina [7117161] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90104612 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Major depressive disorder 83,810 European ancestry cases, 166,405 European ancestry controls NA NR [NR] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90020222 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Depression 55,228 European ancestry cases, 155,103 European ancestry controls NA NR [NR] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90020223 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Depressive symptoms 169,546 European ancestry individuals NA NR [NR] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90020224 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Depressive symptoms 111,268 European ancestry individuals NA NR [NR] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90020225 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Major depressive disorder 25,843 African American cases, 33,757 African American controls NA NR [NR] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90020226 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Major depressive disorder 340,591 European ancestry cases, 813,676 European ancestry controls 455,350 cases, 887,428 controls NR [NR] 117 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90020227 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Depression 312,009 European ancestry cases, 802,374 European ancestry controls NA NR [NR] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90020228 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Depressive symptoms 286,821 European ancestry individuals NA NR [NR] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90020229 Genome-wide genotyping array 2021-09-30 34045744 Levey DF 2021-05-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/34045744 Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. Major depressive disorder 340,591 European ancestry cases, 813,676 European ancestry controls, 25,843 African American cases, 33,757 African American controls NA NR [NR] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90020230 Genome-wide genotyping array 2022-09-08 35841873 Xue Z 2022-07-13 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/35841873 Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. Age-related macular degeneration 5,873 European ancestry cases, 60,514 European ancestry controls NA Affymetrix [8935901] (imputed) 2 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90134545 Genome-wide genotyping array 2022-09-08 35841873 Xue Z 2022-07-13 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/35841873 Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. Diabetic retinopathy 1,652 European ancestry cases, 60,577 European ancestry controls NA Affymetrix [8935901] (imputed) 3 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST90134546 Genome-wide genotyping array 2022-09-08 35841873 Xue Z 2022-07-13 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/35841873 Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. Glaucoma 7,873 European ancestry cases, 60,517 European ancestry controls NA Affymetrix [8935901] (imputed) 18 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90134547 Genome-wide genotyping array 2022-09-08 35841873 Xue Z 2022-07-13 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/35841873 Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. Retinal detachment 3,449 European ancestry cases, 60,562 European ancestry controls NA Affymetrix [8935901] (imputed) 2 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90134548 Genome-wide genotyping array 2022-09-08 35841873 Xue Z 2022-07-13 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/35841873 Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. Myopia 27,993 European ancestry cases, 36,275 European ancestry controls NA Affymetrix [8935901] (imputed) 61 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90134549 Genome-wide genotyping array 2022-09-08 35841873 Xue Z 2022-07-13 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/35841873 Genome-wide association meta-analysis of 88,250 individuals highlights pleiotropic mechanisms of five ocular diseases in UK Biobank. Ocular disease 43,877 European ancestry cases, 44,373 European ancestry controls NA Affymetrix [8935901] (imputed) 37 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90134550 Genome-wide genotyping array 2022-10-21 34047475 Tan C 2021-05-01 Clin Transl Med www.ncbi.nlm.nih.gov/pubmed/34047475 A genome-wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertension. Hypertension 353 Chinese ancestry cases, 332 Chinese ancestry controls 1,592 Chinese ancestry cases, 1,302 Chinese ancestry controls Affymetrix [3956088] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST013041 Genome-wide genotyping array 2022-01-06 34873335 van Rheenen W 2021-12-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34873335 Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Amyotrophic lateral sclerosis 27,205 European ancestry cases, 110,881 European ancestry controls, 2,407 East Asian ancestry cases, 11,775 East Asian ancestry controls NA Illumina [10461755] (imputed) 12 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST90027163 Genome-wide genotyping array 2022-01-06 34873335 van Rheenen W 2021-12-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34873335 Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. Amyotrophic lateral sclerosis 27,205 European ancestry cases, 110,881 European ancestry controls NA Illumina [10461755] (imputed) 16 amyotrophic lateral sclerosis http://purl.obolibrary.org/obo/MONDO_0004976 GCST90027164 Genome-wide genotyping array 2022-01-17 34733494 Nakamura Y 2021-10-11 J Nutr Sci www.ncbi.nlm.nih.gov/pubmed/34733494 A genome-wide association study on meat consumption in a Japanese population: the Japan Multi-Institutional Collaborative Cohort study. Meat consumption 14,076 Japanese ancestry individuals NA Illumina [8503383] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90090964 Genome-wide genotyping array 2022-01-17 34733494 Nakamura Y 2021-10-11 J Nutr Sci www.ncbi.nlm.nih.gov/pubmed/34733494 A genome-wide association study on meat consumption in a Japanese population: the Japan Multi-Institutional Collaborative Cohort study. Meat consumption 6,332 Japanese ancestry males NA Illumina [8503383] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90090965 Genome-wide genotyping array 2022-01-17 34733494 Nakamura Y 2021-10-11 J Nutr Sci www.ncbi.nlm.nih.gov/pubmed/34733494 A genome-wide association study on meat consumption in a Japanese population: the Japan Multi-Institutional Collaborative Cohort study. Meat consumption 7,744 Japanese ancestry females NA Illumina [8503383] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90090966 Genome-wide genotyping array 2022-01-13 29374629 Ortiz-Fernandez L 2018-01-27 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/29374629 Cross-phenotype analysis of Immunochip data identifies KDM4C as a relevant locus for the development of systemic vasculitis. Systemic vasculitis 2,425 European ancestry cases, 4,526 European ancestry controls NA Illumina [191948] 2 vasculitis http://www.ebi.ac.uk/efo/EFO_0006803 GCST012636 Targeted genotyping array [ImmunoChip] 2021-11-25 34624637 Zainul Abidin FN 2021-09-21 Neuroimage Clin www.ncbi.nlm.nih.gov/pubmed/34624637 Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort. Age related hearing loss-related regional glucose metabolism (Bilateral Heschl’s gyrus) 228 European ancestry cases, 587 European ancestry controls NA Illumina [5082878] (imputed) 10 glucose metabolism measurement, age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0009367, http://www.ebi.ac.uk/efo/EFO_0005782 GCST90053841 Genome-wide genotyping array 2021-11-25 34624637 Zainul Abidin FN 2021-09-21 Neuroimage Clin www.ncbi.nlm.nih.gov/pubmed/34624637 Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort. Age related hearing loss-related regional glucose metabolism (Inferior colliculus) 228 European ancestry cases, 587 European ancestry controls NA Illumina [5082878] (imputed) 15 glucose metabolism measurement, age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0009367, http://www.ebi.ac.uk/efo/EFO_0005782 GCST90053842 Genome-wide genotyping array 2021-11-25 34624637 Zainul Abidin FN 2021-09-21 Neuroimage Clin www.ncbi.nlm.nih.gov/pubmed/34624637 Glucose hypometabolism in the Auditory Pathway in Age Related Hearing Loss in the ADNI cohort. Age related hearing loss-related regional glucose metabolism (Cochlear nucleus) 228 European ancestry cases, 587 European ancestry controls NA Illumina [5082878] (imputed) 13 glucose metabolism measurement, age-related hearing impairment http://www.ebi.ac.uk/efo/EFO_0009367, http://www.ebi.ac.uk/efo/EFO_0005782 GCST90053843 Genome-wide genotyping array 2022-06-22 35356681 Fontana V 2022-03-22 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35356681 Chromosomal Region 11p14.1 is Associated with Pharmacokinetics and Pharmacodynamics of Bisoprolol. Bisoprolol clearance in non-ST elevation acute coronary syndrome 622 European ancestry individuals NA Illumina [NR] (imputed) 23 response to beta blocker http://www.ebi.ac.uk/efo/EFO_0007766 GCST90104710 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129851 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair14_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129852 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair15_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129853 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair16_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129854 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair17_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129855 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair18_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129856 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair19_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129857 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair20_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129858 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130163 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130164 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130165 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130166 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130167 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130168 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130169 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130170 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130171 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130172 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130173 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130174 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130175 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130176 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130177 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130178 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130179 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130143 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130144 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130145 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130146 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130147 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130148 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130149 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130150 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130151 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130152 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130153 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130154 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130155 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130156 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130157 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130158 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130159 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130160 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130161 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130162 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129821 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129822 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129823 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129824 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129825 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130180 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130181 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130182 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_26) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130183 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130184 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130185 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130186 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130187 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130188 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130189 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130190 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130191 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130192 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130193 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130194 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130195 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130196 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130197 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130198 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130199 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130200 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130201 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130202 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130203 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_2) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129859 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129826 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129827 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129828 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129829 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129830 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129831 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129832 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair14_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129833 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair15_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129834 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair16_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129835 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair17_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129836 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair18_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129837 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair19_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129838 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129839 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129840 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129841 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129842 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129843 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129844 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129845 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129846 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129847 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129848 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129849 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129850 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_3) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129860 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_3) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129861 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129862 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129863 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_4) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129864 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129865 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129866 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129867 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_5) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129868 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129869 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129870 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129871 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129872 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_6) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129873 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129874 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129875 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129876 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129877 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129878 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_7) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129879 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129880 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129881 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129882 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129883 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129884 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Carotid artery intima-media thickness in type 2 diabetes 838 African American individuals NA Affymetrix, Illumina [19600000] (imputed) 7 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90026645 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Carotid artery intima-media thickness in type 2 diabetes 3,608 European ancestry individuals NA Affymetrix, Illumina [19600000] (imputed) 1 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90026646 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Carotid artery intima-media thickness in type 2 diabetes 3,608 European ancestry individuals, 838 African American individuals NA Affymetrix, Illumina [19600000] (imputed) 3 carotid artery intima media thickness http://www.ebi.ac.uk/efo/EFO_0007117 GCST90026647 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Coronary artery calcification in type 2 diabetes 2,500 European ancestry individuals NA Affymetrix, Illumina [19600000] (imputed) 1 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90026640 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Coronary artery calcification in type 2 diabetes 1,590 African American individuals NA Affymetrix, Illumina [19600000] (imputed) 1 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90026642 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Coronary artery calcification in type 2 diabetes 1,590 African American individuals, 2,500 European ancestry individuals NA Affymetrix, Illumina [19600000] (imputed) 0 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90090961 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Coronary artery calcification in type 2 diabetes (excluding prevalent cardiovascular disease) 1,420 European ancestry individuals NA Affymetrix, Illumina [19600000] (imputed) 3 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90026641 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Coronary artery calcification in type 2 diabetes (excluding prevalent cardiovascular disease) 1,248 African American individuals NA Affymetrix, Illumina [19600000] (imputed) 7 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90026643 Genome-wide genotyping array 2021-11-23 34241534 Lu Y 2021-07-09 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/34241534 Multiethnic Genome-wide Association Study of Subclinical Atherosclerosis in Individuals with Type 2 Diabetes. Coronary artery calcification in type 2 diabetes (excluding prevalent cardiovascular disease) 1,248 African American individuals, 1,420 European ancestry individuals NA Affymetrix, Illumina [19600000] (imputed) 2 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST90026644 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130781 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130782 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130783 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130784 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130785 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130786 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130787 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130788 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130789 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130790 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130791 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130792 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130793 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130794 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130795 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130796 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130797 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130798 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130799 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130800 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130801 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130802 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130803 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130804 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130805 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129910 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129911 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129912 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129913 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129914 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129915 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129916 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129917 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129918 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129919 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129920 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129921 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129922 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129923 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_12) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129924 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129925 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129926 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130286 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130399 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130528 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130529 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130530 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130531 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130532 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130533 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130534 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130535 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130536 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130537 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130538 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130539 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130540 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130541 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130542 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130543 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130544 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130545 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130546 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130547 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130548 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130549 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130550 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130551 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130552 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130553 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130554 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130555 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130556 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130557 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130558 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129944 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130287 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130288 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130289 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130290 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130291 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130292 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130293 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130294 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130295 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130766 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130767 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130768 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130769 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130770 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130771 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130772 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130773 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130774 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130775 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130776 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130777 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130778 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130779 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130780 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130559 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130560 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130561 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130562 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130563 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130564 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130565 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130566 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129927 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129928 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129929 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129930 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129931 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129932 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129933 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129934 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129935 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_13) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129936 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129937 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129938 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129939 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129940 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129941 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129942 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129943 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130806 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130807 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130808 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130809 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130810 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130296 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130297 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130298 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130299 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130300 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130301 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130302 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130303 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130304 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130305 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130306 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130307 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130400 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130401 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130402 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130403 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130404 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130405 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130406 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130407 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130838 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130839 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130840 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130841 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130842 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130843 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130844 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130845 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130846 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair43_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130847 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair44_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130848 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130849 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130850 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130851 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130852 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130853 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130854 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_46) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130855 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129995 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129997 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129999 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130813 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130814 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130815 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130816 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130817 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130818 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130819 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130820 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130821 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130822 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130823 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130824 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130825 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130826 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130827 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130828 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130829 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130830 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130831 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130832 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130833 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130834 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130835 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130836 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130837 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130473 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130474 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130475 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130476 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130477 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130478 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130479 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130480 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130481 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130482 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130483 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130484 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130485 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130486 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130487 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130488 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130489 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130043 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130044 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130045 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130046 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130047 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130048 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130049 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130050 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130026 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130027 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130028 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130029 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130030 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130031 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130032 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130033 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130034 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130035 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130036 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130037 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130038 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130325 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130326 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130327 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130328 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130329 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130330 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130331 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130332 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130333 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130445 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130446 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130447 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130001 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130002 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130003 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130004 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130005 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130006 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130007 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130008 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130009 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130010 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130011 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130012 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130013 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130014 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130015 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130016 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130017 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130018 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130019 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130020 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130021 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130022 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130023 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130024 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130025 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130448 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130449 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130450 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130451 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130452 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130453 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130454 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130455 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130456 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130457 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130458 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130459 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130460 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130461 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130462 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130463 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130464 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130465 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130466 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130467 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130468 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130469 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130470 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130471 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_36) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130472 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129994 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129996 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129998 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130000 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130505 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130506 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130507 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130508 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130509 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130510 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130511 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130512 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130513 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130514 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130515 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130516 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130517 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130518 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130519 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130520 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130521 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130522 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130523 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130524 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130525 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130526 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_38) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130527 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130072 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130073 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130074 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130075 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130076 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130077 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130078 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130079 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130080 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130081 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130082 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130083 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130084 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130085 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130086 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130087 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130088 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130362 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130363 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130364 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130365 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130366 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130367 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130368 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130369 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130370 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130371 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130639 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130640 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130641 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130642 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130643 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130644 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130089 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130090 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130091 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130092 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130093 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130094 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130095 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130096 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130097 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130098 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130099 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130100 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130101 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130102 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130103 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130104 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130105 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130106 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130107 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130372 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130373 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130374 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130375 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130376 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130377 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130378 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130379 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130380 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130381 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130731 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130732 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130733 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130734 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130735 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130736 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130737 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130738 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130739 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130740 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130741 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130742 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130743 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130744 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130745 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130746 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130747 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130748 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130749 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130750 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130751 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130752 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130753 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130754 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130755 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130756 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130757 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130758 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130759 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130760 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair42_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130761 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130762 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130763 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130764 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_44) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130765 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130609 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130610 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130611 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130612 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130613 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130614 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130615 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130616 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130617 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130618 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130619 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130620 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130621 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130622 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130623 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130624 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130625 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130626 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130627 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130628 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130629 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130630 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130631 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130632 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130633 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130634 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130635 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130636 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130637 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130638 Genome-wide genotyping array 2022-07-27 35838494 Hale AT 2022-07-19 Neurosurgery www.ncbi.nlm.nih.gov/pubmed/35838494 Multinational Genome-Wide Association Study and Functional Genomics Analysis Implicates Decreased SIRT3 Expression Underlying Intracranial Aneurysm Risk. Intracranial aneurysm 3,132 European ancestry, East Asian ancestry cases, 152,022 European ancestry, East Asian ancestry controls NA Illumina [NR] (imputed) 4 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90129639 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Direct bilirubin levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90134510 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Aspartate aminotransferase levels 1,988 East Asian ancestry individuals NA NR [9487345] (imputed) 1 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90134511 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Albumin levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 1 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90134512 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Liver enzyme levels (gamma-glutamyl transferase) 5,694 African ancestry individuals NA NR [9487345] (imputed) 1 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90134513 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Total bilirubin levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 2 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90134514 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Glycated hemoglobin levels 1,988 East Asian ancestry individuals NA NR [9487345] (imputed) 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90134515 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Cystatin C levels 1,988 East Asian ancestry individuals NA NR [9487345] (imputed) 1 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90134516 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Urea levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 1 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90134517 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Alanine aminotransferase levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 17 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90134472 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Albumin levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90134473 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Alkaline phosphatase (UKB data field 30610) 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 6 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90134474 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Apolipoprotein A levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90134475 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Apolipoprotein B levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 1 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90134476 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Aspartate aminotransferase levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 8 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90134477 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. High-sensitivity C-reactive protein levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90134478 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Total cholesterol levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90134479 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Creatinine levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90134480 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Cystatin C levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 11 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90134481 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Direct bilirubin levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 6 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90134482 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Liver enzyme levels (gamma-glutamyl transferase) 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 58 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90134483 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Random glucose levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 8 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90134484 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Glycated hemoglobin levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90134485 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. High density lipoprotein cholesterol levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90134486 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Low density lipoprotein cholesterol levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90134487 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Lipoprotein A levels (UKB data field 30790) 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 2 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90134488 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Total bilirubin levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 5 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90134489 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Triglyceride levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals 23,294 European ancestry women NR [9487345] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90134490 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Urea levels 5,694 African ancestry individuals, 1,988 East Asian ancestry individuals, 336,298 European ancestry individuals, 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 1 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90134491 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Glycated hemoglobin levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 9 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90134492 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Cystatin C levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 1 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90134493 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Random glucose levels 1,988 East Asian ancestry individuals NA NR [9487345] (imputed) 1 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90134494 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Glycated hemoglobin levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 5 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90134495 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Aspartate aminotransferase levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 1 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90134496 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Total cholesterol levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 4 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90134497 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Creatinine levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 3 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90134498 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Random glucose levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 4 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90134499 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Total cholesterol levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90134500 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Low density lipoprotein cholesterol levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90134501 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Alanine aminotransferase levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 3 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90134502 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. High density lipoprotein cholesterol levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90134503 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Low density lipoprotein cholesterol levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 3 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90134504 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Random glucose levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 10 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90134505 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Cystatin C levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 1 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90134506 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. High density lipoprotein cholesterol levels 5,694 African ancestry individuals NA NR [9487345] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90134507 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. Aspartate aminotransferase levels 6,036 South Asian ancestry individuals NA NR [9487345] (imputed) 2 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90134508 Genome-wide genotyping array 2022-09-08 35810165 Westerman KE 2022-07-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35810165 Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers. High-sensitivity C-reactive protein levels 1,988 East Asian ancestry individuals NA NR [9487345] (imputed) 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90134509 Genome-wide genotyping array 2022-07-29 35460232 Krupenko SA 2022-04-23 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/35460232 Genetic variants in ALDH1L1 and GLDC influence serine to glycine ratio in Hispanic children. Serine levels 803 Hispanic individuals NA Illumina [889892] 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90129636 Genome-wide genotyping array 2022-07-29 35460232 Krupenko SA 2022-04-23 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/35460232 Genetic variants in ALDH1L1 and GLDC influence serine to glycine ratio in Hispanic children. Glycine levels 803 Hispanic individuals NA Illumina [889892] 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90129637 Genome-wide genotyping array 2022-07-29 35460232 Krupenko SA 2022-04-23 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/35460232 Genetic variants in ALDH1L1 and GLDC influence serine to glycine ratio in Hispanic children. Serine to glycine ratio 803 Hispanic individuals NA Illumina [889892] 14 serine:glycine ratio http://www.ebi.ac.uk/efo/EFO_0021777 GCST90129638 Genome-wide genotyping array 2022-05-13 35136033 Lu Z 2022-02-08 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35136033 ATAD3B and SKIL polymorphisms associated with antipsychotic-induced QTc interval change in patients with schizophrenia: a genome-wide association study. Antipsychotic drug-induced QTc interval change in schizophrenia 2,040 Chinese Han ancestry individuals NA Illumina [7077929] (imputed) 2 heart rate variability measurement, response to antipsychotic drug http://www.ebi.ac.uk/efo/EFO_0008003, http://purl.obolibrary.org/obo/GO_0097332 GCST90102614 Genome-wide genotyping array 2022-09-08 35793696 Kim HK 2022-07-06 Pharmacopsychiatry www.ncbi.nlm.nih.gov/pubmed/35793696 Identification of Endocannabinoid Predictors of Treatment Outcomes in Major Depressive Disorder: A Secondary Analysis of the First Canadian Biomarker Integration Network in Depression (CAN-BIND 1) Study. Response to escitalopram in major depressive disorder 180 European ancestry individuals NA NR [1629536] 0 response to escitalopram http://www.ebi.ac.uk/efo/EFO_0007871 GCST90134434 Genome-wide genotyping array 2022-09-08 35793696 Kim HK 2022-07-06 Pharmacopsychiatry www.ncbi.nlm.nih.gov/pubmed/35793696 Identification of Endocannabinoid Predictors of Treatment Outcomes in Major Depressive Disorder: A Secondary Analysis of the First Canadian Biomarker Integration Network in Depression (CAN-BIND 1) Study. Remission after escitalopram treatment in major depressive disorder 180 European ancestry individuals NA NR [1629536] 0 response to escitalopram http://www.ebi.ac.uk/efo/EFO_0007871 GCST90134435 Genome-wide genotyping array 2022-09-08 35793696 Kim HK 2022-07-06 Pharmacopsychiatry www.ncbi.nlm.nih.gov/pubmed/35793696 Identification of Endocannabinoid Predictors of Treatment Outcomes in Major Depressive Disorder: A Secondary Analysis of the First Canadian Biomarker Integration Network in Depression (CAN-BIND 1) Study. Response to antidepressant treatment in major depressive disorder 166 European ancestry individuals NA NR [1629536] 0 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST90134436 Genome-wide genotyping array 2022-09-08 35793696 Kim HK 2022-07-06 Pharmacopsychiatry www.ncbi.nlm.nih.gov/pubmed/35793696 Identification of Endocannabinoid Predictors of Treatment Outcomes in Major Depressive Disorder: A Secondary Analysis of the First Canadian Biomarker Integration Network in Depression (CAN-BIND 1) Study. Remission after antidepressant treatment in major depressive disorder 166 European ancestry individuals NA NR [1629536] 0 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST90134437 Genome-wide genotyping array 2022-06-20 35637384 Tcheandjieu C 2022-05-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35637384 High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease. Ascending aorta diameter 133 East Asian ancestry individuals NA Illumina [7355269] (imputed) 0 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90091053 Genome-wide genotyping array 2022-06-20 35637384 Tcheandjieu C 2022-05-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35637384 High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease. Ascending aorta diameter 32,215 European ancestry individuals, 262 African American or Afro-Caribbean, Sub-Saharan African ancestry individuals, 421 South Asian ancestry individuals, 133 East Asian ancestry individuals NA Illumina [30943887] (imputed) 3 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90091049 Genome-wide genotyping array 2022-06-20 35637384 Tcheandjieu C 2022-05-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35637384 High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease. Ascending aorta diameter 32,215 European ancestry individuals NA Illumina [9573185] (imputed) 38 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90091050 Genome-wide genotyping array 2022-06-20 35637384 Tcheandjieu C 2022-05-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35637384 High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease. Ascending aorta diameter 262 African American or Afro-Caribbean, Sub-Saharan African ancestry individuals NA Illumina [7650106] (imputed) 13 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90091051 Genome-wide genotyping array 2022-06-20 35637384 Tcheandjieu C 2022-05-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35637384 High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease. Ascending aorta diameter 421 South Asian ancestry individuals NA Illumina [9928046] (imputed) 2 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90091052 Genome-wide genotyping array 2021-11-29 30044860 Fernandez-Rhodes L 2018-07-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/30044860 The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis. Age at menopause 7,928 African American, 5,271 Hispanic, 4,347 Asian American, 184 Native American ancestry women NA Illumina [196483] 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST012557 Targeted genotyping array [Metabochip] 2021-11-29 30044860 Fernandez-Rhodes L 2018-07-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/30044860 The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis. Age at menarche 20,209 African American, 15,347 Hispanic, 8,273 Asian American, 538 Native American ancestry women NA Illumina [196483] 1 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST012556 Targeted genotyping array [Metabochip] 2022-05-06 35079012 Kasai M 2022-01-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35079012 GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion. Acute encephalopathy with biphasic seizures and late reduced diffusion 252 Japanese ancestry cases, 792 Japanese ancestry controls 22 Japanese ancestry cases, 4,773 Japanese ancestry controls Affymetrix [3289568] (imputed) 2 encephalopathy, acute, infection-induced http://purl.obolibrary.org/obo/MONDO_0000166 GCST90102509 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130118 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130119 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130120 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130121 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130122 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130123 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130124 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130125 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130126 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130127 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130128 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130129 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130130 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130131 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130132 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130133 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130134 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130135 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130136 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130137 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130138 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130139 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130140 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130141 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_25) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130142 Genome-wide genotyping array 2022-04-06 34904537 Mone F 2021-12-14 Platelets www.ncbi.nlm.nih.gov/pubmed/34904537 Platelet response to aspirin in UK and Irish pregnancy cohorts: a genome-wide approach. Platelet response to aspirin 182 individuals NA Affymetrix [1283354] (imputed) 12 response to acetylsalicylate http://purl.obolibrary.org/obo/GO_1903492 GCST90101715 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130242 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130243 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129897 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129898 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129899 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129900 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129901 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130244 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130245 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130246 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130247 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130248 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130249 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130250 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130251 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130252 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130253 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130254 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130255 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130256 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130257 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130258 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130259 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130260 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130261 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130217 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130218 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130219 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130220 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130221 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130222 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130223 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130224 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130225 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130226 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130227 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130228 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130229 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130230 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130231 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130232 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130233 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130234 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130235 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130236 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130237 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130238 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130239 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130240 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130241 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130382 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130383 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130384 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130385 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130386 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130387 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130388 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130389 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130390 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130391 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130392 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130393 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130394 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130395 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130396 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130397 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130398 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129902 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129903 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129904 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129905 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129906 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129907 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129908 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_11) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129909 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129885 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_8) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129886 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129887 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129888 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129889 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129890 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129891 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129892 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129893 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_9) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129894 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129895 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_10) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129896 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130204 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130205 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130206 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130207 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130208 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_27) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130209 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130210 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130211 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130212 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130213 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130214 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130215 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_28) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130216 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130262 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130263 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_29) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130264 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130265 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130266 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130267 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130268 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130269 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130270 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130271 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130272 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130273 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130274 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130275 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130276 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130277 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130278 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130279 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130280 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130281 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130282 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130283 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130284 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_30) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130285 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130361 Genome-wide genotyping array 2021-06-01 34002017 Shen S 2021-05-17 NPJ Precis Oncol www.ncbi.nlm.nih.gov/pubmed/34002017 A multi-omics study links TNS3 and SEPT7 to long-term former smoking NSCLC survival. Lung cancer prognosis in former smokers 1,299 European ancestry long-term former smokers NA Illumina [100680] 2 non-small cell lung carcinoma, disease prognosis measurement http://www.ebi.ac.uk/efo/EFO_0003060, http://www.ebi.ac.uk/efo/EFO_0007936 GCST90014045 Targeted genotyping array [Oncoarray] 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130433 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130434 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130435 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130436 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130437 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130438 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130439 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130440 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130441 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130442 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130443 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130444 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129945 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129946 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129947 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129948 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_14) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129949 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129950 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129951 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129952 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129953 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129954 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129955 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129956 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129957 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130656 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130657 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130658 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130659 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130660 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130661 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130662 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130663 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130664 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130665 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130666 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130667 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130668 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130669 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130670 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130671 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130672 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130673 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130674 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130675 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130676 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130677 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130678 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130679 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130680 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130681 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130682 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130683 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130684 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130685 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130686 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130687 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130688 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129987 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129988 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129989 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129990 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129991 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129992 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129993 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130317 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130318 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130319 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130320 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130321 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130322 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130323 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130324 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130811 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_45) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130812 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129983 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129984 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129985 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129986 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130308 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130309 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130310 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130311 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130312 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130313 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130314 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130315 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_31) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130316 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130567 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130645 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130646 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130647 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130648 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130649 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130650 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130651 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130652 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130653 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130654 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_41) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130655 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129958 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129959 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129960 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129961 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129962 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_15) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129963 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129964 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129965 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129966 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129967 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129968 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129969 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129970 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129971 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129972 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129973 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129974 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129975 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129976 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129977 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_16) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129978 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129979 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129980 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129981 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129982 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130408 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130409 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130410 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130411 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130412 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130413 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130414 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130415 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130416 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130417 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130418 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_34) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130419 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130420 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130421 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130422 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130423 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130424 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130425 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130426 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130427 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130428 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130429 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130430 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130431 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_35) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130432 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130051 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130052 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130053 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130054 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130055 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130056 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130057 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130058 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130059 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130060 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130061 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130062 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130063 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130064 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130065 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130039 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130040 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130041 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130042 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130334 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130335 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130336 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130337 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130338 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130339 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130340 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130341 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130342 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130343 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130344 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130345 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130346 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 1 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130689 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130690 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130691 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130692 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130693 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130694 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130695 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130696 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130697 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130698 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130699 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130700 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130701 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130702 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130703 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130704 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130705 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130706 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130605 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130606 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130607 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130608 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130066 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130067 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_21) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130068 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130069 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130070 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_22) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130071 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130490 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130491 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130492 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130493 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130494 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130495 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130496 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130497 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130498 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130499 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130500 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130501 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130502 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130503 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_37) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130504 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130348 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130349 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130350 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130351 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130352 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130353 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130354 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130355 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130356 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130357 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130358 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130359 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_33) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130360 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130568 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130569 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130570 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130571 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130572 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130573 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130574 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130575 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130576 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130577 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130578 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130579 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130580 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130581 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130582 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130583 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130584 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130585 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130586 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130587 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130588 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130589 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130590 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130591 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130592 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130593 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130594 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130595 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130596 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130597 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130598 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_39) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130599 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130600 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130601 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130602 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130603 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_40) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130604 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130707 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130708 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130709 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130710 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130711 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130712 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130713 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130714 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130715 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130716 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair39_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130717 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair40_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130718 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair41_42) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130719 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130720 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130721 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130722 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130723 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130724 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130725 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130726 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130727 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130728 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130729 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_43) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130730 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_32) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130347 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130108 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130109 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130110 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_23) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130111 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130112 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130113 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130114 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130115 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130116 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_24) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130117 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair15_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129783 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair16_17) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129784 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129785 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129786 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129787 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129788 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129789 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129790 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129791 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129792 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129793 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129794 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129795 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129796 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129797 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair14_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129798 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair15_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129799 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair16_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129800 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair17_18) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129801 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129802 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair2_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129803 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair3_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129804 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair4_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129805 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair5_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129806 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair6_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129807 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair7_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129808 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair8_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129809 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair9_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129810 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair10_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129811 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair11_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129812 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair12_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129813 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair13_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129814 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair14_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129815 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair15_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129816 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair16_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129817 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair17_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129818 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair18_19) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129819 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net25_Pair1_20) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90129820 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair46_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131080 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair47_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131081 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair48_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131082 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair49_50) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131083 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair1_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131084 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair2_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131085 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair3_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131086 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair4_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131087 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair5_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131088 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair6_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131089 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair7_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131090 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair8_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131091 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130931 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130922 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130923 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130924 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130925 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130926 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130927 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130928 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130929 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_47) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90130930 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair9_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131092 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair10_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131093 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair11_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131094 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair12_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131095 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair13_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131096 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair14_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131097 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair15_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131098 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair16_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131099 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair17_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131100 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair18_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131101 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair19_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131102 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair20_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131103 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair21_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131104 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair22_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131105 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair23_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131106 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair24_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131107 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair25_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131108 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair26_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131109 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair27_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131110 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair28_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131111 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair29_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131112 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair30_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131113 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair31_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131114 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair32_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131115 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair33_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131116 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair34_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131117 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair35_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131118 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair36_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131119 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair37_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131120 Genome-wide genotyping array 2022-07-29 35393594 Zhao B 2022-04-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35393594 Common variants contribute to intrinsic human brain functional networks. Brain rsFMRI measurement (functional connectivity) (Net100_Pair38_51) 34,691 British ancestry individuals 9,882 European ancestry individuals, 1,489 Caribbean, African American ancestry individuals, 768 Hispanic or Latin American individuals, 446 Indian, Pakistani,Bangladeshi, Chinese ancestry individuals NR [9026427] (imputed) 0 functional brain measurement http://www.ebi.ac.uk/efo/EFO_0007849 GCST90131121 Genome-wide genotyping array 2021-07-07 34111113 Green HD 2021-06-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34111113 A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor. Frozen shoulder 451,099 European ancestry individuals NA NR [8274682] (imputed) 0 frozen shoulder http://www.ebi.ac.uk/efo/EFO_1000941 GCST90000512 Genome-wide genotyping array 2021-07-07 34111113 Green HD 2021-06-10 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/34111113 A genome-wide association study identifies 5 loci associated with frozen shoulder and implicates diabetes as a causal risk factor. Frozen shoulder 627,998 European ancestry individuals NA NR [16689279] (imputed) 5 frozen shoulder http://www.ebi.ac.uk/efo/EFO_1000941 GCST90000513 Genome-wide genotyping array 2022-07-27 35459784 Aggarwal P 2022-04-22 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35459784 Genetic susceptibility to patient-reported xerostomia among long-term oropharyngeal cancer survivors. Xerostomia (moderate to severe) in oropharyngeal cancer 138 moderate to severe xerostomia cases, 214 none to mild xerostomia controls NA Illumina [579956] 5 xerostomia http://www.ebi.ac.uk/efo/EFO_0009869 GCST90129633 Genome-wide genotyping array 2021-08-13 34315874 Ward LD 2021-07-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34315874 GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms. Extrahepatic cholangiocarcinoma 148 British ancestry cases, 408,035 British ancestry controls NA Affymetrix [11811438] (imputed) 2 extrahepatic bile duct carcinoma http://purl.obolibrary.org/obo/MONDO_0003090 GCST90013662 Genome-wide genotyping array 2021-08-13 34315874 Ward LD 2021-07-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34315874 GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms. Alanine aminotransferase levels 387,859 British ancestry individuals, 10,635 Asian or Asian British individuals, 7,468 Black or Black British individuals, 2,338 Chinese ancestry individuals NA Affymetrix [21347608] (imputed) 104 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90013663 Genome-wide genotyping array 2021-08-13 34315874 Ward LD 2021-07-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34315874 GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms. Aspartate aminotransferase levels 386,570 British ancestry individuals, 10,617 Asian or Asian British individuals, 7,426 Black or Black British individuals, 2,321 Chinese ancestry individuals NA Affymetrix [21347608] (imputed) 103 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90013664 Genome-wide genotyping array 2022-11-01 34083597 Kolifarhood G 2021-06-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34083597 Genome-wide association study on blood pressure traits in the Iranian population suggests ZBED9 as a new locus for hypertension. Systolic blood pressure 4,567 Iranian ancestry individuals 1,618 Iranian ancestry individuals Illumina [616263] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90020043 Genome-wide genotyping array 2022-11-01 34083597 Kolifarhood G 2021-06-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34083597 Genome-wide association study on blood pressure traits in the Iranian population suggests ZBED9 as a new locus for hypertension. Diastolic blood pressure 4,567 Iranian ancestry individuals 1,618 Iranian ancestry individuals Illumina [616263] (imputed) 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90020044 Genome-wide genotyping array 2022-11-01 34083597 Kolifarhood G 2021-06-03 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34083597 Genome-wide association study on blood pressure traits in the Iranian population suggests ZBED9 as a new locus for hypertension. Hypertension 4,214 Iranian ancestry individuals 1,618 Iranian ancestry individuals Illumina [616308] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90020045 Genome-wide genotyping array 2021-07-27 32882024 Lee SHR 2020-09-03 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/32882024 Genome-wide association study of susceptibility loci for TCF3-PBX1 acute lymphoblastic leukemia in children. Childhood acute lymphoblastic leukemia (TCF3-PBX1 fusion) 40 European ancestry cases, 2,057 European ancestry controls 28 African American cases, 1,380 African American controls, 30 Hispanic cases, 682 Hispanic controls, 24 cases, 1,399 controls Affymetrix [7528340] (imputed) 1 B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) http://purl.obolibrary.org/obo/MONDO_0600030 GCST90020048 Genome-wide genotyping array 2021-07-27 32882024 Lee SHR 2020-09-03 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/32882024 Genome-wide association study of susceptibility loci for TCF3-PBX1 acute lymphoblastic leukemia in children. TCF3-PBX1 fusion in childhood acute lymphoblastic leukemia 40 European ancestry cases, 1,454 European ancestry controls 28 African American cases, 186 African American controls, 30 Hispanic cases, 424 Hispanic controls, 24 cases, 343 controls Affymetrix [7550069] (imputed) 1 B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) http://purl.obolibrary.org/obo/MONDO_0600030 GCST90020049 Genome-wide genotyping array 2022-11-18 34234248 Razzaq M 2021-07-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34234248 An artificial neural network approach integrating plasma proteomics and genetic data identifies PLXNA4 as a new susceptibility locus for pulmonary embolism. Venous thrombosis or pulmonary embolism 481 deep vein thrombosis cases, 93 pulmonary embolism cases 1,414 deep vein thrombosis cases, 467 pulmonary embolism cases Illumina [NR] (imputed) 0 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST013056 Genome-wide genotyping array 2021-10-08 34155719 Margaritte-Jeannin P 2021-06-22 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/34155719 Identification of OCA2 as a novel locus for the co-morbidity of asthma-plus-eczema. Asthma and eczema 1,208 European ancestry cases with both asthma and eczema, 7,599 European ancestry controls with neither asthma nor eczema NA Illumina [NR] (imputed) 4 asthma, Eczema http://purl.obolibrary.org/obo/MONDO_0004979, http://purl.obolibrary.org/obo/HP_0000964 GCST012462 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. Anti-BK polyomavirus IgG seropositivity 14,249 European ancestry antibody-positive cases, up to 1,154 European ancestry antibody-negative controls NA Affymetrix [NR] (imputed) 0 BK polyomavirus seropositivity http://www.ebi.ac.uk/efo/EFO_0010905 GCST90032662 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. BK polyomavirus VP1 antibody levels 14,249 European ancestry individuals NA Affymetrix [NR] (imputed) 1 anti-BK polyomavirus antibody measurement http://www.ebi.ac.uk/efo/EFO_0010904 GCST90032663 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. Anti-human polyomavirus 6 IgG seropositivity 5,094 European ancestry antibody-positive cases, up to 958 European ancestry antibody-negative controls NA Affymetrix [NR] (imputed) 0 human polyomavirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0600072 GCST90032664 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. Human polyomavirus 6 VP1 antibody levels 5,094 European ancestry individuals NA Affymetrix [NR] (imputed) 5 anti-human polyomavirus 6 antibody measurement http://www.ebi.ac.uk/efo/EFO_0600074 GCST90032665 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. Anti-JC polyomavirus IgG seropositivity 8,567 European ancestry antibody-positive cases cases, up to 6,836 European ancestry antibody-negative controls NA Affymetrix [NR] (imputed) 19 polyomavirus 2 seropositivity http://www.ebi.ac.uk/efo/EFO_0010907 GCST90032666 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. JC polyomavirus VP1 antibody levels 8,567 European ancestry individuals NA Affymetrix [NR] (imputed) 7 anti-polyomavirus 2 antibody measurement http://www.ebi.ac.uk/efo/EFO_0010900 GCST90032667 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. Anti-Merkel cell polyomavirus IgG seropositivity 8,091 European ancestry antibody-positive cases, up to 3,623 European ancestry antibody-negative controls NA Affymetrix [NR] (imputed) 14 merkel cell virus seropositivity http://www.ebi.ac.uk/efo/EFO_0010906 GCST90032668 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. Merkel cell polyomavirus VP1 antibody levels 8,091 European ancestry individuals NA Affymetrix [NR] (imputed) 15 anti-merkel cell virus antibody measurement http://www.ebi.ac.uk/efo/EFO_0010899 GCST90032669 Genome-wide genotyping array 2021-10-21 34532061 Hodel F 2021-06-11 Virus Evol www.ncbi.nlm.nih.gov/pubmed/34532061 Human genomics of the humoral immune response against polyomaviruses. WU polyomavirus VP1 antibody levels 5,791 European ancestry individuals NA Affymetrix [NR] (imputed) 1 anti-WU polyomavirus antibody measurement http://www.ebi.ac.uk/efo/EFO_0600073 GCST90032670 Genome-wide genotyping array 2021-08-13 34319380 Gaitanidis A 2021-07-28 JAMA Surg www.ncbi.nlm.nih.gov/pubmed/34319380 Association Between NEDD4L Variation and the Genetic Risk of Acute Appendicitis: A Multi-institutional Genome-Wide Association Study. Acute appendicitis 1,743 European or unknown ancestry cases, 27,963 European or unknown ancestry controls NA Illumina [5676600] (imputed) 1 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90013428 Genome-wide genotyping array 2021-07-07 34127828 Bolin K 2021-06-14 Genes Immun www.ncbi.nlm.nih.gov/pubmed/34127828 Variants in BANK1 are associated with lupus nephritis of European ancestry. Lupus nephritis in systemic lupus erythematosus 377 European ancestry cases, 714 European ancestry controls 570 Europen ancestry cases, 1,225 European ancestry controls Illumina [112815] 1 lupus nephritis http://www.ebi.ac.uk/efo/EFO_0005761 GCST012003 Targeted genotyping array [ImmunoChip] 2021-10-18 34050765 Zhang L 2021-05-29 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/34050765 Joint genome-wide association analyses identified 49 novel loci for age at natural menopause. Age at menopause 181,219 European ancestry individuals NA Illumina [2398641] (imputed) 51 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90026597 Genome-wide genotyping array 2021-10-18 34050765 Zhang L 2021-05-29 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/34050765 Joint genome-wide association analyses identified 49 novel loci for age at natural menopause. Age at menopause 181,219 European ancestry individuals, 43,861 East Asian ancestry individuals NA Illumina [2093892] (imputed) 46 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90026598 Genome-wide genotyping array 2022-06-22 35313970 Dong Q 2022-03-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/35313970 Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer. Epigenetic age acceleration (Hannum) in childhood cancer survivors 2,640 European ancestry individuals NA Illumina [8300000] 1 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104781 Genome-wide sequencing 2022-06-22 35313970 Dong Q 2022-03-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/35313970 Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer. Epigenetic age acceleration (Horvath) in childhood cancer survivors 2,640 European ancestry individuals NA Illumina [8300000] 1 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104782 Genome-wide sequencing 2022-06-22 35313970 Dong Q 2022-03-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/35313970 Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer. Epigenetic age acceleration (PhenoAge) in childhood cancer survivors 2,640 European ancestry individuals NA Illumina [8300000] 0 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104783 Genome-wide sequencing 2022-06-22 35313970 Dong Q 2022-03-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/35313970 Genome-wide association studies identify novel genetic loci for epigenetic age acceleration among survivors of childhood cancer. Epigenetic age acceleration (GrimAge) in childhood cancer survivors 2,640 European ancestry individuals NA Illumina [8300000] 0 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104784 Genome-wide sequencing 2021-11-01 34488071 Crist RC 2021-08-28 Drug Alcohol Depend www.ncbi.nlm.nih.gov/pubmed/34488071 Analysis of genetic and clinical factors associated with buprenorphine response. Response to buprenorphine in opioid use disorder 1,609 European ancestry individuals NA Affymetrix [NR] (imputed) 6 response to opioid http://www.ebi.ac.uk/efo/EFO_0008541 GCST90044777 Genome-wide genotyping array 2021-09-30 34032881 Du M 2021-05-25 Intensive Care Med www.ncbi.nlm.nih.gov/pubmed/34032881 Integrative omics provide biological and clinical insights into acute respiratory distress syndrome. Acute respiratory distress syndrome 1,250 European ancestry cases, 1,583 European ancestry controls, 387 African American cases, 387 African American controls NA Illumina [3817416] (imputed) 3 acute respiratory distress syndrome http://www.ebi.ac.uk/efo/EFO_1000637 GCST012418 Genome-wide genotyping array 2021-09-29 34337522 van der Zanden LFM 2021-04-24 Eur Urol Open Sci www.ncbi.nlm.nih.gov/pubmed/34337522 CDH12 as a Candidate Gene for Kidney Injury in Posterior Urethral Valve Cases: A Genome-wide Association Study Among Patients with Obstructive Uropathies. Kidney injury 5 years post-surgery in obstructive uropathies 141 European ancestry cases, 216 European ancestry controls NA Illumina [622697] (imputed) 3 kidney injury http://www.ebi.ac.uk/efo/EFO_0009833 GCST90025931 Genome-wide genotyping array 2021-08-23 33640202 Kim BH 2021-02-03 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/33640202 Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease. Left inferior frontal gyrus (orbital part) cortical thickness 919 European ancestry individuals 629 individuals Illumina [3041429] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90025855 Genome-wide genotyping array 2021-08-23 33640202 Kim BH 2021-02-03 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/33640202 Genome-wide association study identifies susceptibility loci of brain atrophy to NFIA and ST18 in Alzheimer's disease. Left parahippocampal gyrus cortical thickness 919 European ancestry individuals 629 individuals Illumina [3041429] (imputed) 1 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90025856 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Liver volume 32,860 European ancestry individuals NA Affymetrix [9390170] (imputed) 12 liver volume http://www.ebi.ac.uk/efo/EFO_0600048 GCST90016666 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Spleen volume 32,860 European ancestry individuals NA Affymetrix [9390170] (imputed) 40 spleen volume http://www.ebi.ac.uk/efo/EFO_0600047 GCST90016667 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Lung volume 32,860 European ancestry individuals NA Affymetrix [9390170] (imputed) 7 lung volume http://www.ebi.ac.uk/efo/EFO_0600046 GCST90016668 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Pancreas volume 31,758 European ancestry individuals NA Affymetrix [9390170] (imputed) 17 pancreas volume http://www.ebi.ac.uk/efo/EFO_0600045 GCST90016669 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Kidney volume 32,860 European ancestry individuals NA Affymetrix [9390170] (imputed) 12 kidney volume http://www.ebi.ac.uk/efo/EFO_0600044 GCST90016670 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Visceral adipose tissue volume 32,860 European ancestry individuals NA Affymetrix [9390170] (imputed) 6 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90016671 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Abdominal subcutaneous adipose tissue volume 32,860 European ancestry individuals NA Affymetrix [9390170] (imputed) 2 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST90016672 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Percent liver fat 32,858 European ancestry individuals NA Affymetrix [9390170] (imputed) 12 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90016673 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Liver iron content 32,858 European ancestry individuals NA Affymetrix [9390170] (imputed) 23 liver iron measurement http://www.ebi.ac.uk/efo/EFO_0010056 GCST90016674 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Pancreas fat 25,617 European ancestry individuals NA Affymetrix [9390170] (imputed) 10 pancreas fat measurement http://www.ebi.ac.uk/efo/EFO_0600049 GCST90016675 Genome-wide genotyping array 2021-08-13 34128465 Liu Y 2021-06-15 Elife www.ncbi.nlm.nih.gov/pubmed/34128465 Genetic architecture of 11 organ traits derived from abdominal MRI using deep learning. Pancreas iron content 25,617 European ancestry individuals NA Affymetrix [9390170] (imputed) 1 iron biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004461 GCST90016676 Genome-wide genotyping array 2021-07-07 34127677 Choquet H 2021-06-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34127677 A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects. Cataracts 28,092 non-Hispanic White ancestry cases, 50,487 non-Hispanic White ancestry controls, 2,233 East Asian ancestry cases, 7,023 East Asian ancestry controls, 2,149 Hispanic/Latino cases, 6,620 Hispanic/Latino controls, 815 African American cases, 2,368 African American controls, 31,852 European ancestry cases, 428,084 European ancestry controls, 757 African ancestry cases, 7,897 African ancestry controls, 1,278 South Asian ancestry cases, 8,571 South Asian ancestry controls, 668 other admixed cases, 7,349 other admixed controls 313,278 European ancestry cases, 2,210,509 European ancestry controls, 7,715 African American cases, 120,390 African American controls, 3,934 East Asian ancestry cases, 104,766 East Asian ancestry controls, 21,408 Latino cases, 425,544 Latino controls, 874 South Asian ancestry cases, 26,037 South Asian ancestry controls Affymetrix [9869154] (imputed) 43 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90014268 Genome-wide genotyping array 2021-07-07 34127677 Choquet H 2021-06-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34127677 A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects. Cataracts 28,092 non-Hispanic White ancestry cases, 50,487 non-Hispanic White ancestry controls, 31,852 European ancestry cases, 428,084 European ancestry controls NA Affymetrix [9869154] (imputed) 49 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST012012 Genome-wide genotyping array 2021-07-07 34127677 Choquet H 2021-06-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34127677 A large multiethnic GWAS meta-analysis of cataract identifies new risk loci and sex-specific effects. Cataracts 38,996 female cases, 283,185 female controls, 28,848 male cases, 234,414 male controls 211,030 female cases, 1,623,785 female controls, 136,179 male cases, 1,263,461 male controls Affymetrix [9869154] (imputed) 26 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST012013 Genome-wide genotyping array 2021-08-24 33331911 Freidin MB 2020-12-17 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/33331911 An association between chronic widespread pain and the gut microbiome. Coprococcus comes 3,521 European or unknown ancestry individuals NA NR [4841651] (imputed) 9 gut microbiome measurement http://www.ebi.ac.uk/efo/EFO_0007874 GCST90025871 Genome-wide genotyping array 2021-08-24 33331911 Freidin MB 2020-12-17 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/33331911 An association between chronic widespread pain and the gut microbiome. Chronic widespread musculoskeletal pain up to 531 European or unknown ancestry cases, up to 2,742 European or unknown ancestry controls NA NR [4841651] (imputed) 15 chronic widespread pain http://www.ebi.ac.uk/efo/EFO_0010099 GCST90025872 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Number of natural teeth 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 number of teeth measurement http://www.ebi.ac.uk/efo/EFO_0010073 GCST011877 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Body mass index 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST011876 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Height 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST011875 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Hip circumference adjusted for BMI 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST011874 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Waist circumference adjusted for body mass index 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST011873 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Waist-hip ratio 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST011872 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Diastolic blood pressure 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST011871 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Systolic blood pressure 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST011870 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Ferritin levels 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST011869 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Iron status biomarkers (transferrin levels) 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 transferrin measurement http://www.ebi.ac.uk/efo/EFO_0006341 GCST011868 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Iron status biomarkers (total iron binding capacity) 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 total iron binding capacity http://www.ebi.ac.uk/efo/EFO_0006334 GCST011867 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Glycated hemoglobin levels 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST011866 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. High density lipoprotein cholesterol levels 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST011865 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Low density lipoprotein cholesterol levels 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST011864 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Triglycerides 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011863 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Total cholesterol levels 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST011862 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Heart rate 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST011861 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. QT interval 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST011860 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. PR interval 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST011859 Genome-wide genotyping array 2021-06-14 30653739 Sofer T 2019-01-17 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30653739 A fully adjusted two-stage procedure for rank-normalization in genetic association studies. Mean corpuscular hemoglobin concentration 12,595 Hispanic individuals NA Illumina [at least 2232944] (imputed) 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST011858 Genome-wide genotyping array 2021-10-21 34177453 Swart PC 2021-06-10 Front Neurosci www.ncbi.nlm.nih.gov/pubmed/34177453 A Genome-Wide Association Study and Polygenic Risk Score Analysis of Posttraumatic Stress Disorder and Metabolic Syndrome in a South African Population. Post-traumatic stress disorder 260 South African Colored cases, 343 South African Colored controls NA Illumina [11927194] (imputed) 7 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90020063 Genome-wide genotyping array 2022-11-17 34217363 Horimoto ARVR 2021-07-03 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/34217363 Admixture mapping reveals the association between Native American ancestry at 3q13.11 and reduced risk of Alzheimer's disease in Caribbean Hispanics. Alzheimer's disease 1,174 Caribbean Hispanics ancestry cases, 1,391 Caribbean Hispanics ancestry controls NA NR [931670] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90025857 Genome-wide genotyping array 2021-08-13 33055079 Boer CG 2020-10-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33055079 Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene. Hand osteoarthritis severity (hand Klsum) 4,829 Dutch ancestry individuals 1,203 individuals Illumina [10500000] (imputed) 2 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90010716 Genome-wide genotyping array 2021-08-13 33055079 Boer CG 2020-10-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33055079 Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene. Finger osteoarthritis severity (hand Klsum) 1,791 Dutch ancestry individuals 1,203 individuals Illumina [10500000] (imputed) 4 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90010717 Genome-wide genotyping array 2021-08-13 33055079 Boer CG 2020-10-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/33055079 Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene. Thumb osteoarthritis severity (hand Klsum) 2,071 Dutch ancestry individuals 1,203 individuals Illumina [10500000] (imputed) 3 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90010718 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Body fat percentage 442,278 European ancestry individuals NA NR [NR] (imputed) 254 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90020232 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. High density lipoprotein cholesterol levels 392,965 European ancestry individuals NA NR [NR] (imputed) 94 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90020233 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Sex hormone-binding globulin levels 389,354 European ancestry individuals NA NR [NR] (imputed) 71 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90020234 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Triglycerides 429,011 European ancestry individuals NA NR [NR] (imputed) 77 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90020235 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Alanine aminotransferase levels 429,203 European ancestry individuals NA NR [NR] (imputed) 55 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90020236 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Aspartate aminotransferase levels 424,778 European ancestry individuals NA NR [NR] (imputed) 36 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90020237 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Visceral adipose tissue 32,859 European ancestry individuals NA NR [NR] (imputed) 0 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90038587 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Subcutaneous adipose tissue 32,859 European ancestry individuals NA NR [NR] (imputed) 0 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST90038588 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Visceral adipose tissue/subcutaneous adipose tissue ratio 32,859 European ancestry individuals NA NR [NR] (imputed) 0 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST90038589 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Pancreas fat 24,673 European ancestry individuals NA NR [NR] (imputed) 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90038590 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Percent liver fat 32,655 European ancestry individuals NA NR [NR] (imputed) 0 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90038591 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Pancreas volume 31,758 European ancestry individuals NA NR [NR] (imputed) 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90038592 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Liver volume 32,859 European ancestry individuals NA NR [NR] (imputed) 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90038593 Genome-wide genotyping array 2021-10-18 33980691 Martin S 2021-05-12 Diabetes www.ncbi.nlm.nih.gov/pubmed/33980691 Genetic evidence for different adiposity phenotypes and their opposing influence on ectopic fat and risk of cardiometabolic disease. Metabolic biomarkers (multivariate analysis) 389,354 European ancestry individuals NA NR [NR] (imputed) 254 aspartate aminotransferase measurement, serum alanine aminotransferase measurement, low density lipoprotein triglyceride measurement, body fat percentage, high density lipoprotein cholesterol measurement, sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004736, http://www.ebi.ac.uk/efo/EFO_0004735, http://www.ebi.ac.uk/efo/EFO_0009946, http://www.ebi.ac.uk/efo/EFO_0007800, http://www.ebi.ac.uk/efo/EFO_0004612, http://www.ebi.ac.uk/efo/EFO_0004696 GCST90038594 Genome-wide genotyping array 2021-10-18 34046847 Yao Y 2021-05-27 Endocrine www.ncbi.nlm.nih.gov/pubmed/34046847 Evaluate the effects of serum urate level on bone mineral density: a genome-wide gene-environment interaction analysis in UK Biobank cohort. Heel bone mineral density x serum urate levels interaction 110,465 men, 127,334 women NA Affymetrix [NR] (imputed) 161 heel bone mineral density, urate measurement http://www.ebi.ac.uk/efo/EFO_0009270, http://www.ebi.ac.uk/efo/EFO_0004531 GCST012489 Genome-wide genotyping array 2021-10-18 34046847 Yao Y 2021-05-27 Endocrine www.ncbi.nlm.nih.gov/pubmed/34046847 Evaluate the effects of serum urate level on bone mineral density: a genome-wide gene-environment interaction analysis in UK Biobank cohort. L1-L4 bone mineral density x serum urate levels interaction 2,207 men, 2,354 women NA Affymetrix [NR] (imputed) 46 urate measurement, spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0004531, http://www.ebi.ac.uk/efo/EFO_0007701 GCST012488 Genome-wide genotyping array 2021-10-18 34046847 Yao Y 2021-05-27 Endocrine www.ncbi.nlm.nih.gov/pubmed/34046847 Evaluate the effects of serum urate level on bone mineral density: a genome-wide gene-environment interaction analysis in UK Biobank cohort. Femur bone mineral density x serum urate levels interaction 2,225 men, 2,350 women NA Affymetrix [NR] (imputed) 653 urate measurement, bone density http://www.ebi.ac.uk/efo/EFO_0004531, http://www.ebi.ac.uk/efo/EFO_0003923 GCST012490 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Body mass index 21,930 Taiwanese ancestry individuals NA Affymetrix [6546460] (imputed) 44 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90103751 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Body fat percentage 21,304 Taiwanese ancestry individuals NA Affymetrix [6546460] (imputed) 17 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90103752 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Waist circumference 21,949 Taiwanese ancestry individuals NA Affymetrix [6546460] (imputed) 30 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90103753 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Waist-hip ratio 21,972 Taiwanese ancestry individuals NA Affymetrix [6546460] (imputed) 25 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90103754 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Body mass index 195,070 Taiwanese ancestry, Japanese ancestry individuals, 334,487 European ancestry, Latino, East Asian ancestry, African American, South Asian ancestry individuals, 361,194 individuals NA Affymetrix [NR] (imputed) 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90103755 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Body fat percentage 21,304 Taiwanese ancestry individuals, 361,194 individuals, 155,961 European ancestry individuals NA Affymetrix [NR] (imputed) 3 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90103756 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Waist circumference 21,949 Taiwanese ancestry individuals, 361,194 individuals, 224,459 European ancestry individuals NA Affymetrix [NR] (imputed) 2 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90103757 Genome-wide genotyping array 2022-05-20 35051171 Wong HS 2022-01-20 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35051171 Genome-wide association study identifies genetic risk loci for adiposity in a Taiwanese population. Waist-hip ratio 21,972 Taiwanese ancestry individuals, 361,194 individuals, 224,459 European ancestry individuals NA Affymetrix [NR] (imputed) 1 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90103758 Genome-wide genotyping array 2022-06-20 33188205 Cai L 2020-11-13 Sci Data www.ncbi.nlm.nih.gov/pubmed/33188205 Genome-wide association analysis of type 2 diabetes in the EPIC-InterAct study. Type 2 diabetes 9,978 European ancestry cases, 12,348 European ancestry controls NA Illumina [8919079] (imputed) 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90006934 Genome-wide genotyping array, Exome genotyping array [Illumina660W-Quad BeadChip | Illumina core-exome 12v1 and 24v1] 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Salad dressing liking 159,310 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094822 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Salad leaves liking 159,482 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094823 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-salad vegetables liking (derived food-liking factor) 159,432 European ancestry individuals NA Affymetrix [9600849] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094824 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Salami liking 154,673 European ancestry individuals NA Affymetrix [11353280] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094825 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Salmon liking 158,673 European ancestry individuals NA Affymetrix [11353280] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094826 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-salty food liking (derived food-liking factor) 156,509 European ancestry individuals NA Affymetrix [9614419] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094827 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Salty food liking 159,571 European ancestry individuals NA Affymetrix [11353280] (imputed) 14 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094828 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Salty pretzels liking 150,683 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094829 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Sardines liking 157,340 European ancestry individuals NA Affymetrix [11353280] (imputed) 16 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094830 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-sauces liking (derived food-liking factor) 158,928 European ancestry individuals NA Affymetrix [9614119] (imputed) 7 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094831 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Sausages liking 158,603 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094832 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-savoury food liking (derived food-liking factor) 157,915 European ancestry individuals NA Affymetrix [9551341] (imputed) 17 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094833 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Savoury biscuit liking 159,272 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094834 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-savour/caloric food liking (derived food-liking factor) 158,684 European ancestry individuals NA Affymetrix [9538018] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094835 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-seafood liking (derived food-liking factor) 156,740 European ancestry individuals NA Affymetrix [9618964] (imputed) 27 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094836 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-sharp flavour liking (derived food-liking factor) 152,547 European ancestry individuals NA Affymetrix [9605914] (imputed) 31 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094837 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Shellfish liking 155,491 European ancestry individuals NA Affymetrix [11353280] (imputed) 28 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094838 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Skimmed milk liking 158,613 European ancestry individuals NA Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094839 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-small fish liking (derived food-liking factor) 150,746 European ancestry individuals NA Affymetrix [9605657] (imputed) 21 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094840 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Smoked fish liking 158,149 European ancestry individuals NA Affymetrix [11353280] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094841 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-sodas liking (derived food-liking factor) 157,911 European ancestry individuals NA Affymetrix [9618746] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094842 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Soft cheese liking 159,253 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094843 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Soy sauce liking 157,246 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094844 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Soya milk liking 113,425 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094845 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Spicy food liking 159,503 European ancestry individuals NA Affymetrix [11353280] (imputed) 14 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094846 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-glutamate liking (derived food-liking factor) 159,473 European ancestry individuals NA Affymetrix [9613983] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094772 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Goat cheese liking 150,875 European ancestry individuals NA Affymetrix [11353280] (imputed) 6 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094773 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Grapefruit liking 157,662 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094774 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Green olives liking 156,731 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094775 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Haddock liking 158,385 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094776 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Ham liking 158,550 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094777 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Hard cheese liking 159,351 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094778 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-healthy food liking (derived food-liking factor) 150,899 European ancestry individuals NA Affymetrix [9599928] (imputed) 7 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094779 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-healthy breakfast food liking (derived food-liking factor) 143,879 European ancestry individuals NA Affymetrix [9613993] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094780 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Herring liking 150,609 European ancestry individuals NA Affymetrix [11353280] (imputed) 20 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094781 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Honey liking 159,091 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094782 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Horseradish liking 152,847 European ancestry individuals NA Affymetrix [11353280] (imputed) 18 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094783 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Ice cream liking 159,498 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094784 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-highly palatable foods liking (derived food-liking factor) 158,666 European ancestry individuals NA Affymetrix [9404854] (imputed) 16 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094785 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Jam liking 159,573 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094786 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Ketchup liking 159,380 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094787 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Kiwi liking 157,218 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094788 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Lager liking 156,958 European ancestry individuals NA Affymetrix [11353280] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094789 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Lamb liking 158,453 European ancestry individuals NA Affymetrix [11353280] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094790 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-acquired taste liking (derived food-liking factor) 156,639 European ancestry individuals NA Affymetrix [9389114] (imputed) 32 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094791 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Lemon liking 159,451 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094792 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-lentils/beans liking (derived food-liking factor) 159,108 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094793 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Liver liking 158,306 European ancestry individuals NA Affymetrix [11353280] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094794 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-low caloric food liking (derived food-liking factor) 154,998 European ancestry individuals NA Affymetrix [9506023] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094795 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Mackerel liking 156,695 European ancestry individuals NA Affymetrix [11353280] (imputed) 14 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094796 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Spinach liking 157,978 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094847 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Spirits liking 157,793 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094848 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Strawberries liking 159,446 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094849 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-strong alcohol liking (derived food-liking factor) 157,348 European ancestry individuals NA Affymetrix [9618688] (imputed) 6 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094850 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-strong flavour liking (derived food-liking factor) 153,924 European ancestry individuals NA Affymetrix [9535166] (imputed) 32 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094851 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-strong vegetable liking (derived food-liking factor) 147,344 European ancestry individuals NA Affymetrix [9601173] (imputed) 22 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094852 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-sweetened coffee drink liking (derived food-liking factor) 148,801 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094853 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-sweet food liking (derived food-liking factor) 159,527 European ancestry individuals NA Affymetrix [11353280] (imputed) 13 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094854 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Tea difference liking 157,305 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094855 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Tea max liking 158,918 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094856 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Tea with sugar liking 158,151 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094857 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Tea without sugar liking 158,072 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094858 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Tinned tuna liking 158,261 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094859 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Tomatoes liking 159,419 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094860 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Turnip liking 155,376 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094861 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Vegetables liking 159,475 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094862 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-vegetarian liking (derived food-liking factor) 159,098 European ancestry individuals NA Affymetrix [9533556] (imputed) 13 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094863 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Vinegar liking 159,565 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094864 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. White bread liking 159,491 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094865 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. White rice liking 159,499 European ancestry individuals NA Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094866 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. White wine liking 158,532 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 white wine liking measurement http://www.ebi.ac.uk/efo/EFO_0006948 GCST90094867 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-whole food liking (derived food-liking factor) 157,918 European ancestry individuals NA Affymetrix [9613644] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094868 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Whole grain cereal liking 157,610 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094869 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Whole milk liking 159,170 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094870 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Wholemeal bread liking 159,342 European ancestry individuals NA Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094871 Genome-wide genotyping array 2022-10-11 35974141 Lahti J 2022-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35974141 Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Verbal short term memory 44,874 European ancestry individuals 8,763 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 32 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST90162631 Genome-wide genotyping array 2022-10-11 35974141 Lahti J 2022-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35974141 Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Verbal learning 28,909 European ancestry individuals 3,853 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 131 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90162632 Genome-wide genotyping array 2022-10-11 35974141 Lahti J 2022-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35974141 Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Verbal short term memory (paragraph recall test) 19,662 European ancestry individuals 4,293 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 93 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST90162633 Genome-wide genotyping array 2022-10-11 35974141 Lahti J 2022-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35974141 Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Verbal short term memory (work list recall test) 25,316 European ancestry individuals 4,293 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST90162634 Genome-wide genotyping array 2022-10-11 35974141 Lahti J 2022-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35974141 Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Verbal learning (oral presentation) 12,593 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 5 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90162635 Genome-wide genotyping array 2022-10-11 35974141 Lahti J 2022-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/35974141 Genome-wide meta-analyses reveal novel loci for verbal short-term memory and learning. Verbal learning (visual presentation) 16,191 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 13 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90162636 Genome-wide genotyping array 2022-07-26 35449187 Kim Y 2022-04-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35449187 Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways. Actinic keratosis 21,462 European ancestry cases, 70,778 European ancestry controls NA Affymetrix, Illumina [6920000] (imputed) 11 actinic keratosis http://www.ebi.ac.uk/efo/EFO_0002496 GCST90095184 Genome-wide genotyping array 2022-07-26 35449187 Kim Y 2022-04-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35449187 Genome-wide association study of actinic keratosis identifies new susceptibility loci implicated in pigmentation and immune regulation pathways. Actinic keratosis 16,352 European ancestry cases, 46,758 European ancestry controls 5,110 European ancestry cases, 24,020 European ancestry controls Affymetrix [NR] (imputed) 6 actinic keratosis http://www.ebi.ac.uk/efo/EFO_0002496 GCST90129628 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2 to 4) (donor effect) 2,355 European ancestry donors 1,570 European ancestry donors Affymetrix, Illumina [NR] (imputed) 1 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102555 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2 to 4) (recipient effect) 2,285 European ancestry recipients 1,523 European ancestry recipients Affymetrix, Illumina [NR] (imputed) 2 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102573 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2 to 4) (donor effect) 1,096 European ancestry sibling donors 684 European ancestry sibling donors Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102561 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2 to 4) (recipient effect) 993 European ancestry sibling recipients 662 European ancestry sibling recipients Affymetrix, Illumina [NR] (imputed) 3 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102579 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2 to 4) (donor effect) 799 European ancestry unrelated donors 533 European ancestry unrelated donors Affymetrix, Illumina [NR] (imputed) 2 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102567 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2 to 4) (recipient effect) 789 European ancestry unrelated recipients 526 European ancestry unrelated recipients Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102585 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2b to 4) (donor effect) 2,386 European ancestry donors 1,591 European ancestry donors Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102556 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2b to 4) (recipient effect) 2,560 European ancestry recipients 1,290 European ancestry recipients Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102574 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2b to 4) (donor effect) 781 European ancestry sibling donors 521 European ancestry sibling donors Affymetrix, Illumina [NR] (imputed) 1 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102562 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2b to 4) (recipient effect) 710 European ancestry sibling recipients 473 European ancestry sibling recipients Affymetrix, Illumina [NR] (imputed) 1 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102580 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2b to 4) (donor effect) 884 European ancestry unrelated donors 454 European ancestry unrelated donors Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102568 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 2b to 4) (recipient effect) 784 European ancestry unrelated recipients 522 European ancestry unrelated recipients Affymetrix, Illumina [NR] (imputed) 2 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102586 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 3 to 4) (donor effect) 1,655 European ancestry donors 1,103 European ancestry donors Affymetrix, Illumina [NR] (imputed) 1 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102557 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 3 to 4) (recipient effect) 2,288 European ancestry recipients 1,526 European ancestry recipients Affymetrix, Illumina [NR] (imputed) 5 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102575 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 3 to 4) (donor effect) 1,096 European ancestry sibling donors 684 European ancestry sibling donors Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102563 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 3 to 4) (recipient effect) 1,006 European ancestry sibling recipients 670 European ancestry sibling recipients Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102581 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 3 to 4) (donor effect) 884 European ancestry unrelated donors 454 European ancestry unrelated donors Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102569 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (stage 3 to 4) (recipient effect) 789 European ancestry unrelated recipients 526 European ancestry unrelated recipients Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102587 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (gut) (donor effect) 2,342 European ancestry donors 1,562 European ancestry donors Affymetrix, Illumina [NR] (imputed) 2 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102558 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (gut) (recipient effect) 2,279 European ancestry recipients 1,519 European ancestry recipients Affymetrix, Illumina [NR] (imputed) 1 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102576 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (gut) (donor effect) 782 European ancestry sibling donors 521 European ancestry sibling donors Affymetrix, Illumina [NR] (imputed) 2 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102564 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (gut) (recipient effect) 1,006 European ancestry sibling recipients 670 European ancestry sibling recipients Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102582 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (gut) (donor effect) 884 European ancestry unrelated donors 454 European ancestry unrelated donors Affymetrix, Illumina [NR] (imputed) 0 acute graft vs. host disease, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004599, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102570 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Acute graft-versus-host disease (gut) (recipient effect) 575 European ancestry unrelated recipients 384 European ancestry unrelated recipients Affymetrix, Illumina [NR] (imputed) 3 acute graft vs. host disease http://www.ebi.ac.uk/efo/EFO_0004599 GCST90102588 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Chronic graft-versus-host disease (donor effect) 2,341 European ancestry donors 1,561 European ancestry donors Affymetrix, Illumina [NR] (imputed) 2 donor genotype effect measurement, chronic graft versus host disease http://www.ebi.ac.uk/efo/EFO_0007892, http://purl.obolibrary.org/obo/MONDO_0020547 GCST90102559 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Chronic graft-versus-host disease (recipient effect) 2,205 European ancestry recipients 1,470 European ancestry recipients Affymetrix, Illumina [NR] (imputed) 1 chronic graft versus host disease http://purl.obolibrary.org/obo/MONDO_0020547 GCST90102577 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Chronic graft-versus-host disease (donor effect) 1,066 European ancestry sibling donors 711 European ancestry sibling donors Affymetrix, Illumina [NR] (imputed) 1 donor genotype effect measurement, chronic graft versus host disease http://www.ebi.ac.uk/efo/EFO_0007892, http://purl.obolibrary.org/obo/MONDO_0020547 GCST90102565 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Chronic graft-versus-host disease (recipient effect) 717 European ancestry sibling recipients 1,271 European ancestry sibling recipients Affymetrix, Illumina [NR] (imputed) 0 chronic graft versus host disease http://purl.obolibrary.org/obo/MONDO_0020547 GCST90102583 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Chronic graft-versus-host disease (donor effect) 802 European ancestry unrelated donors 535 European ancestry unrelated donors Affymetrix, Illumina [NR] (imputed) 2 donor genotype effect measurement, chronic graft versus host disease http://www.ebi.ac.uk/efo/EFO_0007892, http://purl.obolibrary.org/obo/MONDO_0020547 GCST90102571 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Chronic graft-versus-host disease (recipient effect) 574 European ancestry unrelated recipients 383 European ancestry unrelated recipients Affymetrix, Illumina [NR] (imputed) 2 chronic graft versus host disease http://purl.obolibrary.org/obo/MONDO_0020547 GCST90102589 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Relapse after allogeneic hematopoietic cell transplantation (donor effect) 1,682 European ancestry donors 1,122 European ancestry donors Affymetrix, Illumina [NR] (imputed) 1 disease recurrence, response to allogeneic hematopoietic stem cell transplant, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102560 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Relapse after allogeneic hematopoietic cell transplantation (recipient effect) 2,560 European ancestry recipients 1,290 European ancestry recipients Affymetrix, Illumina [NR] (imputed) 0 disease recurrence, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90102578 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Relapse after allogeneic hematopoietic cell transplantation (donor effect) 1,096 European ancestry sibling donors 684 European ancestry sibling donors Affymetrix, Illumina [NR] (imputed) 0 disease recurrence, response to allogeneic hematopoietic stem cell transplant, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102566 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Relapse after allogeneic hematopoietic cell transplantation (recipient effect) 1,006 European ancestry sibling recipients 670 European ancestry sibling recipients Affymetrix, Illumina [NR] (imputed) 0 disease recurrence, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90102584 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Relapse after allogeneic hematopoietic cell transplantation (donor effect) 802 European ancestry unrelated donors 535 European ancestry unrelated donors Affymetrix, Illumina [NR] (imputed) 3 disease recurrence, response to allogeneic hematopoietic stem cell transplant, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0007044, http://www.ebi.ac.uk/efo/EFO_0007892 GCST90102572 Genome-wide genotyping array 2022-07-20 34996099 Martin PJ 2022-01-07 Blood Adv www.ncbi.nlm.nih.gov/pubmed/34996099 Genetic Associations with Immune-mediated Outcomes after Allogeneic Hematopoietic Cell Transplantation. Relapse after allogeneic hematopoietic cell transplantation (recipient effect) 789 European ancestry unrelated recipients 526 European ancestry unrelated recipients Affymetrix, Illumina [NR] (imputed) 2 disease recurrence, response to allogeneic hematopoietic stem cell transplant http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0007044 GCST90102590 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 11,778 European ancestry cases, 357,198 European ancestry controls, 4,893 Black cases, 94,556 Black controls, 2,497 Hispanic cases, 41,100 Hispanic controls NA Affymetrix [NR] (imputed) 3 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103486 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 11,778 European ancestry cases, 357,198 European ancestry controls NA Affymetrix [NR] (imputed) 3 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103487 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 4,893 Black cases, 94,556 Black controls NA Affymetrix [NR] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103488 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 2,497 Hispanic cases, 41,100 Hispanic controls NA Affymetrix [NR] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103489 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs population) 2,417 European ancestry cases, 366,449 European ancestry controls, 1,300 Black cases, 98,129 Black controls, 517 Hispanic cases, 43,062 Hispanic controls NA Affymetrix [NR] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103490 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs population) 2,417 European ancestry cases, 366,449 European ancestry controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103491 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs population) 1,300 Black cases, 98,129 Black controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103492 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs population) 517 Hispanic cases, 43,062 Hispanic controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103493 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs not hospitalized) 2,417 European ancestry cases, 9,361 European ancestry controls, 1,300 Black cases, 3,593 Black controls, 517 Hispanic cases, 1,980 Hispanic controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103494 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs not hospitalized) 2,417 European ancestry cases, 9,361 European ancestry controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103495 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs not hospitalized) 1,300 Black cases, 3,593 Black controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103496 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (hospitalized vs not hospitalized) 517 Hispanic cases, 1,980 Hispanic controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103497 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (severe vs population) 543 European ancestry cases, 368,433 European ancestry controls, 284 Black cases, 99,165 Black controls, 120 Hispanic cases, 43,477 Hispanic controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103498 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (severe vs population) 543 European ancestry cases, 368,433 European ancestry controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103499 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (severe vs population) 284 Black cases, 99,165 Black controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103500 Genome-wide genotyping array 2022-05-17 35222515 Peloso GM 2022-02-03 Front Genet www.ncbi.nlm.nih.gov/pubmed/35222515 Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program. COVID-19 (severe vs population) 120 Hispanic cases, 43,477 Hispanic controls NA Affymetrix [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90103501 Genome-wide genotyping array 2023-06-20 36747015 Kopylov AT 2023-02-06 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36747015 Consolidation of metabolomic, proteomic, and GWAS data in connective model of schizophrenia. Schizophrenia 49 European ancestry cases, 50 European ancestry controls 28 European ancestry cases, 11 European ancestry controls Illumina [652297] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90270906 Genome-wide genotyping array 2022-12-13 34320236 Sun YV 2021-07-28 Mov Disord www.ncbi.nlm.nih.gov/pubmed/34320236 A Multi-center Genome-wide Association Study of Cervical Dystonia. Cervical dystonia 919 European ancestry cases, 1,491 European ancestry controls 473 cases, 481 controls Illumina [8053795] (imputed) 0 cervical dystonia http://purl.obolibrary.org/obo/MONDO_0000481 GCST90027049 Genome-wide genotyping array 2022-12-13 34320236 Sun YV 2021-07-28 Mov Disord www.ncbi.nlm.nih.gov/pubmed/34320236 A Multi-center Genome-wide Association Study of Cervical Dystonia. Cervical dystonia (age at onset) 919 European ancestry individuals NA Illumina [8053795] (imputed) 1 age of onset of cervical dystonia http://purl.obolibrary.org/obo/OBA_2040167 GCST90027050 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 126 cholesteryl ester measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092846 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 92 cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020944, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092847 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 116 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092848 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 88 free cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020945, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092849 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 113 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092850 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of large HDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 122 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092851 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 104 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092852 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 87 phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020946, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092853 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 76 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092854 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in large HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 93 triglycerides:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092855 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 63 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092856 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 76 cholesterol:total lipids ratio, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092857 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 61 cholesteryl ester measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092858 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 48 low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90092859 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 72 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092860 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 102 low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90092861 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 62 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092862 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of large LDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 67 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092863 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 61 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092864 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 56 low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90092865 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 80 triglyceride measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092866 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in large LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 85 triglycerides:total lipids ratio, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092867 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 82 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092868 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in large VLDL 115,071 European ancestry individuals NA NR [11722792] (imputed) 61 very low density lipoprotein cholesterol measurement, cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020943 GCST90092869 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 80 cholesteryl ester measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092870 Genome-wide genotyping array 2022-03-04 34754074 Grgic O 2021-11-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/34754074 CYP11B1 variants influence skeletal maturation via alternative splicing. Skeletal age 4,557 European, African, Asian and unknown ancestry individuals NA Illumina [9806907] (imputed) 6 skeletal age http://www.ebi.ac.uk/efo/EFO_0020898 GCST90095044 Genome-wide genotyping array 2022-04-29 34982741 Bruggemann A 2022-01-04 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/34982741 Risk of Revision After Arthroplasty Associated with Specific Gene Loci: A Genomewide Association Study of Single-Nucleotide Polymorphisms in 1,130 Twins Treated with Arthroplasty. Revision surgery due to aseptic loosening after total joint arthroplasty 75 cases from twins, 1,036 controls from twins NA Illumina [14548648] (imputed) 11 revision of total joint arthroplasty, aseptic loosening http://www.ebi.ac.uk/efo/EFO_0020974, http://www.ebi.ac.uk/efo/EFO_0010725 GCST90102256 Genome-wide genotyping array 2022-04-29 34982741 Bruggemann A 2022-01-04 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/34982741 Risk of Revision After Arthroplasty Associated with Specific Gene Loci: A Genomewide Association Study of Single-Nucleotide Polymorphisms in 1,130 Twins Treated with Arthroplasty. Revision surgery after total joint arthroplasty 94 cases from twins, 1,036 controls from twins NA Illumina [14548648] (imputed) 20 revision of total joint arthroplasty http://www.ebi.ac.uk/efo/EFO_0020974 GCST90102257 Genome-wide genotyping array 2022-04-29 34982741 Bruggemann A 2022-01-04 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/34982741 Risk of Revision After Arthroplasty Associated with Specific Gene Loci: A Genomewide Association Study of Single-Nucleotide Polymorphisms in 1,130 Twins Treated with Arthroplasty. Revision surgery due to aseptic loosening after total hip arthroplasty 51 cases from twins, 621 controls from twins NA Illumina [14548648] (imputed) 24 revision of total hip arthroplasty, aseptic loosening http://www.ebi.ac.uk/efo/EFO_0020973, http://www.ebi.ac.uk/efo/EFO_0010725 GCST90102258 Genome-wide genotyping array 2022-04-29 34982741 Bruggemann A 2022-01-04 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/34982741 Risk of Revision After Arthroplasty Associated with Specific Gene Loci: A Genomewide Association Study of Single-Nucleotide Polymorphisms in 1,130 Twins Treated with Arthroplasty. Revision surgery after total hip arthroplasty 64 cases from twins, 621 controls from twins NA Illumina [14548648] (imputed) 9 revision of total hip arthroplasty http://www.ebi.ac.uk/efo/EFO_0020973 GCST90102259 Genome-wide genotyping array 2022-04-29 34982741 Bruggemann A 2022-01-04 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/34982741 Risk of Revision After Arthroplasty Associated with Specific Gene Loci: A Genomewide Association Study of Single-Nucleotide Polymorphisms in 1,130 Twins Treated with Arthroplasty. Revision surgery due to aseptic loosening after total knee arthroplasty 25 cases from twins, 487 controls from twins NA Illumina [14548648] (imputed) 29 aseptic loosening, revision of total knee arthroplasty http://www.ebi.ac.uk/efo/EFO_0010725, http://www.ebi.ac.uk/efo/EFO_0020972 GCST90102260 Genome-wide genotyping array 2022-04-29 34982741 Bruggemann A 2022-01-04 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/34982741 Risk of Revision After Arthroplasty Associated with Specific Gene Loci: A Genomewide Association Study of Single-Nucleotide Polymorphisms in 1,130 Twins Treated with Arthroplasty. Revision surgery after total knee arthroplasty 32 cases from twins, 487 controls from twins NA Illumina [14548648] (imputed) 20 revision of total knee arthroplasty http://www.ebi.ac.uk/efo/EFO_0020972 GCST90102261 Genome-wide genotyping array 2022-03-08 34592243 Nusinovici S 2021-09-27 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/34592243 High-density lipoprotein 3 cholesterol and primary open-angle glaucoma: metabolomics and mendelian randomization analyses. High-density lipoprotein 3 cholesterol levels 2,308 Chinese ancestry individuals, 2,528 Indian ancestry individuals, 2,521 Malays ancestry individuals, 10,984 Finnish ancestry individuals NA Illumina [NR] (imputed) 11 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90095140 Genome-wide genotyping array, Exome-wide sequencing 2022-05-06 35074609 Shen Y 2022-01-19 Thromb Res www.ncbi.nlm.nih.gov/pubmed/35074609 Whole exome sequencing identifies genetic variants in Chinese Han pregnant women with venous thromboembolism. Venous thromboembolism in pregnancy 24 Han Chinese ancestry cases, 24 Han Chinese ancestry controls NA Illumina [344571] 4 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90102508 Exome-wide sequencing 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in large VLDL 115,071 European ancestry individuals NA NR [11722792] (imputed) 71 very low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90092871 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 86 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092872 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in large VLDL 115,071 European ancestry individuals NA NR [11722792] (imputed) 54 very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90092873 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 89 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092874 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of large VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 90 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092875 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 89 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092876 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in large VLDL 115,071 European ancestry individuals NA NR [11722792] (imputed) 92 very low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90092877 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in large VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 87 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092878 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in large VLDL 115,071 European ancestry individuals NA NR [11722792] (imputed) 62 triglycerides:total lipids ratio, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092879 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Ratio of linoleic acid to total fatty acids 115,006 European ancestry individuals NA NR [11722792] (imputed) 42 fatty acid measurement, linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0005110, http://www.ebi.ac.uk/efo/EFO_0006807 GCST90092881 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 62 cholesteryl ester measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092884 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 62 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092885 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 63 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092886 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of LDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 66 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092887 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 61 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092888 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Average diameter for LDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 38 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90092889 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 90 triglyceride measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092890 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 101 cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092893 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 89 cholesteryl ester measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092894 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 98 cholesteryl esters:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020944, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092895 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 90 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092896 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 112 free cholesterol:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020945, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092897 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 80 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092898 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 78 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092900 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 102 phospholipids:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020946, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092901 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 77 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092902 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in medium HDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 96 triglycerides:total lipids ratio, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90092903 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 57 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092904 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 43 cholesterol:total lipids ratio, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020943, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092905 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 53 cholesteryl ester measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092906 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 49 low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90092907 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 62 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092908 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 94 low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90092909 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 58 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092910 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of medium LDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 51 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092911 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 58 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092912 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 47 low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90092913 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 93 triglyceride measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092914 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglycerides to total lipids ratio in medium LDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 81 triglycerides:total lipids ratio, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0020947, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90092915 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol levels in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 63 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092916 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesterol to total lipids ratio in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 98 very low density lipoprotein cholesterol measurement, cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020943 GCST90092917 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl ester levels in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 61 cholesteryl ester measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010351, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092918 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Cholesteryl esters to total lipids ratio in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 92 very low density lipoprotein cholesterol measurement, cholesteryl esters:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020944 GCST90092919 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol levels in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 67 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092920 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Free cholesterol to total lipids ratio in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 82 very low density lipoprotein cholesterol measurement, free cholesterol:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020945 GCST90092921 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Total lipid levels in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 76 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90092922 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Concentration of medium VLDL particles 115,082 European ancestry individuals NA NR [11722792] (imputed) 71 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092923 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipid levels in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 68 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90092924 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Phospholipids to total lipids ratio in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 75 very low density lipoprotein cholesterol measurement, phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0020946 GCST90092925 Genome-wide genotyping array 2022-04-27 35213538 Richardson TG 2022-02-25 PLoS Biol www.ncbi.nlm.nih.gov/pubmed/35213538 Characterising metabolomic signatures of lipid-modifying therapies through drug target mendelian randomisation. Triglyceride levels in medium VLDL 115,082 European ancestry individuals NA NR [11722792] (imputed) 86 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90092926 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2593) 2,466 Black/admixed ancestry individuals NA Illumina [149527] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177537 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2599) 2,466 Black/admixed ancestry individuals NA Illumina [149648] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177538 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2599) 2,466 Black/admixed ancestry individuals NA Illumina [153209] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178842 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI261) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152481] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177539 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2612) 2,466 Black/admixed ancestry individuals NA Illumina [152792] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177540 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI262) 2,466 Black/admixed ancestry individuals NA Illumina [155077] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177541 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2626) 2,466 Black/admixed ancestry individuals NA Illumina [149609] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177542 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI263) 2,466 Black/admixed ancestry individuals NA Illumina [154930] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177543 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2639) 2,466 Black/admixed ancestry individuals NA Illumina [155602] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177544 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2648) 2,466 Black/admixed ancestry individuals NA Illumina [163958] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177545 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI265) 2,466 Black/admixed ancestry individuals NA Illumina [159384] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177546 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2408) 2,466 Black/admixed ancestry individuals NA Illumina [161334] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177502 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI241) 2,466 Black/admixed ancestry individuals NA Illumina [154491] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177503 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2418) 2,466 Black/admixed ancestry individuals NA Illumina [150491] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177504 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2418) 2,466 Black/admixed ancestry individuals NA Illumina [153759] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178838 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI243) 2,466 Black/admixed ancestry individuals NA Illumina [152406] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177505 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2432) 2,466 Black/admixed ancestry individuals NA Illumina [149929] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177506 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2435) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155415] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177507 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI244) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153888] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177508 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2451) 2,466 Black/admixed ancestry individuals NA Illumina [152801] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177509 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2457) 2,466 Black/admixed ancestry individuals NA Illumina [173208] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177510 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2468) 2,466 Black/admixed ancestry individuals NA Illumina [173508] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177511 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2471) 2,466 Black/admixed ancestry individuals NA Illumina [143503] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179041 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. SDMA levels 2,466 Black/admixed ancestry individuals NA Illumina [155212] 0 symmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006523 GCST90178693 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Serine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152847] 3 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90178694 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Serotonin levels 2,466 Black/admixed ancestry individuals NA Illumina [155096] 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90178695 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Simvastatin levels 2,466 Black/admixed ancestry individuals NA Illumina [149577] 0 simvastatin measurement http://www.ebi.ac.uk/efo/EFO_0801219 GCST90176128 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Sphinganine levels 2,466 Black/admixed ancestry individuals NA Illumina [161048] 0 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90178696 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Stearic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157359] 1 stearic acid measurement http://www.ebi.ac.uk/efo/EFO_0801220 GCST90176104 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Succinic acid/Methylmalonic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156545] 1 Succinic acid measurement, Methylmalonic acid measurement http://www.ebi.ac.uk/efo/EFO_0021669, http://www.ebi.ac.uk/efo/EFO_0021651 GCST90176075 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. T4 levels 2,466 Black/admixed ancestry individuals NA Illumina [144981] 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90176105 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Taurine levels 2,466 Black/admixed ancestry individuals NA Illumina [151918] 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90176076 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Taurine levels 2,466 Black/admixed ancestry individuals NA Illumina [152995] 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90178697 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Taurocholic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [190614] 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90176077 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Taurodeoxycholic acid/Taurochenodeoxycholic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [159359] 0 taurochenodeoxycholate measurement, taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537, http://www.ebi.ac.uk/efo/EFO_0010539 GCST90176078 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Thiamine levels 2,466 Black/admixed ancestry individuals NA Illumina [146329] 0 thiamine measurement http://www.ebi.ac.uk/efo/EFO_0010540 GCST90178698 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2183) 2,466 Black/admixed ancestry individuals NA Illumina [150064] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177459 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2187) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156343] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177460 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2188) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159159] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177461 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2190) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160652] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177462 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI220) 2,466 Black/admixed ancestry individuals NA Illumina [150284] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177463 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2202) 2,466 Black/admixed ancestry individuals NA Illumina [151664] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177464 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2217) 2,466 Black/admixed ancestry individuals NA Illumina [171054] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177465 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2220) 2,466 Black/admixed ancestry individuals NA Illumina [150635] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177466 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2222) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [166862] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177467 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2223) 2,466 Black/admixed ancestry individuals NA Illumina [153383] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177468 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2235) 2,466 Black/admixed ancestry individuals NA Illumina [167407] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177469 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2236) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149504] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177470 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2239) 2,466 Black/admixed ancestry individuals NA Illumina [161007] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177471 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI224) 2,466 Black/admixed ancestry individuals NA Illumina [171231] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177472 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2240) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148989] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177473 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2241) 2,466 Black/admixed ancestry individuals NA Illumina [154172] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177474 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2242) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159710] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177475 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2243) 2,466 Black/admixed ancestry individuals NA Illumina [164665] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177476 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2243) 2,466 Black/admixed ancestry individuals NA Illumina [158950] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179037 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2254) 2,466 Black/admixed ancestry individuals NA Illumina [160151] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177477 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2256) 2,466 Black/admixed ancestry individuals NA Illumina [149483] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177478 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2258) 2,466 Black/admixed ancestry individuals NA Illumina [146110] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177479 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI226) 2,466 Black/admixed ancestry individuals NA Illumina [163897] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177480 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2269) 2,466 Black/admixed ancestry individuals NA Illumina [167322] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177481 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI228) 2,466 Black/admixed ancestry individuals NA Illumina [156320] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177482 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2033) 2,466 Black/admixed ancestry individuals NA Illumina [157673] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177440 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2036) 2,466 Black/admixed ancestry individuals NA Illumina [174023] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177441 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI204) 2,466 Black/admixed ancestry individuals NA Illumina [157498] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177442 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI204) 2,466 Black/admixed ancestry individuals NA Illumina [155912] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178832 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2044) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150760] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177443 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2046) 2,466 Black/admixed ancestry individuals NA Illumina [149772] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177444 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2049) 2,466 Black/admixed ancestry individuals NA Illumina [149230] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177445 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2067) 2,466 Black/admixed ancestry individuals NA Illumina [155694] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177446 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2067) 2,466 Black/admixed ancestry individuals NA Illumina [162567] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178833 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2072) 2,466 Black/admixed ancestry individuals NA Illumina [143462] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177447 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2082) 2,466 Black/admixed ancestry individuals NA Illumina [157106] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177448 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2082) 2,466 Black/admixed ancestry individuals NA Illumina [147552] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179034 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2089) 2,466 Black/admixed ancestry individuals NA Illumina [150927] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177449 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2098) 2,466 Black/admixed ancestry individuals NA Illumina [151521] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177450 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2099) 2,466 Black/admixed ancestry individuals NA Illumina [150317] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177451 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2106) 2,466 Black/admixed ancestry individuals NA Illumina [156148] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177452 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2106) 2,466 Black/admixed ancestry individuals NA Illumina [156954] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178834 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI212) 2,466 Black/admixed ancestry individuals NA Illumina [155021] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177453 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2146) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151143] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177454 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2159) 2,466 Black/admixed ancestry individuals NA Illumina [169766] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177455 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2160) 2,466 Black/admixed ancestry individuals NA Illumina [166755] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177456 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2163) 2,466 Black/admixed ancestry individuals NA Illumina [320227] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179035 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2166) 2,466 Black/admixed ancestry individuals NA Illumina [175569] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179036 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2179) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155186] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177457 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2180) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153371] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177458 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2281) 2,466 Black/admixed ancestry individuals NA Illumina [133127] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177483 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2282) 2,466 Black/admixed ancestry individuals NA Illumina [173398] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177484 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI229) 2,466 Black/admixed ancestry individuals NA Illumina [152247] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177485 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2291) 2,466 Black/admixed ancestry individuals NA Illumina [155416] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177486 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2291) 2,466 Black/admixed ancestry individuals NA Illumina [160996] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179038 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2297) 2,466 Black/admixed ancestry individuals NA Illumina [165266] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177487 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI230) 2,466 Black/admixed ancestry individuals NA Illumina [162114] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177488 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2306) 2,466 Black/admixed ancestry individuals NA Illumina [140933] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177489 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI232) 2,466 Black/admixed ancestry individuals NA Illumina [174866] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177490 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2320) 2,466 Black/admixed ancestry individuals NA Illumina [157298] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177491 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2320) 2,466 Black/admixed ancestry individuals NA Illumina [149938] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178835 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2322) 2,466 Black/admixed ancestry individuals NA Illumina [145147] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177492 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2334) 2,466 Black/admixed ancestry individuals NA Illumina [145179] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177493 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2334) 2,466 Black/admixed ancestry individuals NA Illumina [162925] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179039 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2341) 2,466 Black/admixed ancestry individuals NA Illumina [145744] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177494 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2351) 2,466 Black/admixed ancestry individuals NA Illumina [172909] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177495 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2351) 2,466 Black/admixed ancestry individuals NA Illumina [146431] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178836 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2364) 2,466 Black/admixed ancestry individuals NA Illumina [146009] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177496 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI237) 2,466 Black/admixed ancestry individuals NA Illumina [162385] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177497 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2379) 2,466 Black/admixed ancestry individuals NA Illumina [137571] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177498 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2379) 2,466 Black/admixed ancestry individuals NA Illumina [138609] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179040 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI238) 2,466 Black/admixed ancestry individuals NA Illumina [160919] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177499 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2384) 2,466 Black/admixed ancestry individuals NA Illumina [148017] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177500 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2384) 2,466 Black/admixed ancestry individuals NA Illumina [149168] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178837 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI24) 2,466 Black/admixed ancestry individuals NA Illumina [152147] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177501 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15853) 2,466 Black/admixed ancestry individuals NA Illumina [144282] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177294 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15854) 2,466 Black/admixed ancestry individuals NA Illumina [155923] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177295 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15855) 2,466 Black/admixed ancestry individuals NA Illumina [150647] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177296 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1586) 2,466 Black/admixed ancestry individuals NA Illumina [154408] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177297 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15860) 2,466 Black/admixed ancestry individuals NA Illumina [150030] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177298 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15861) 2,466 Black/admixed ancestry individuals NA Illumina [171525] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179014 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15867) 2,466 Black/admixed ancestry individuals NA Illumina [153557] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177299 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15869) 2,466 Black/admixed ancestry individuals NA Illumina [152033] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177300 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15873) 2,466 Black/admixed ancestry individuals NA Illumina [152231] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177301 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15875) 2,466 Black/admixed ancestry individuals NA Illumina [153947] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177302 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1588) 2,466 Black/admixed ancestry individuals NA Illumina [160672] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179015 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15885) 2,466 Black/admixed ancestry individuals NA Illumina [143580] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177303 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15886) 2,466 Black/admixed ancestry individuals NA Illumina [157118] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177304 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15887) 2,466 Black/admixed ancestry individuals NA Illumina [151769] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177305 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15888) 2,466 Black/admixed ancestry individuals NA Illumina [160989] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177306 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15891) 2,466 Black/admixed ancestry individuals NA Illumina [148521] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177307 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15895) 2,466 Black/admixed ancestry individuals NA Illumina [150953] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177308 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15899) 2,466 Black/admixed ancestry individuals NA Illumina [155643] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177309 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15901) 2,466 Black/admixed ancestry individuals NA Illumina [153618] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177310 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15902) 2,466 Black/admixed ancestry individuals NA Illumina [156737] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177311 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15904) 2,466 Black/admixed ancestry individuals NA Illumina [145266] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177312 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15914) 2,466 Black/admixed ancestry individuals NA Illumina [155755] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177313 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15919) 2,466 Black/admixed ancestry individuals NA Illumina [160357] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177314 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15920) 2,466 Black/admixed ancestry individuals NA Illumina [150155] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177315 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15925) 2,466 Black/admixed ancestry individuals NA Illumina [149684] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177316 Genome-wide sequencing 2022-08-16 34534736 Care AG 2021-08-18 Eur J Obstet Gynecol Reprod Biol www.ncbi.nlm.nih.gov/pubmed/34534736 Maternal selenium levels and whole genome screen in recurrent spontaneous preterm birth population: A nested case control study. Midgestational selenium levels 301 European ancestry individuals NA Affymetrix [NR] (imputed) 1 selenium measurement http://www.ebi.ac.uk/efo/EFO_0006331 GCST90032671 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI256) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155255] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177531 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2565) 2,466 Black/admixed ancestry individuals NA Illumina [144747] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177532 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2569) 2,466 Black/admixed ancestry individuals NA Illumina [152366] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177533 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI257) 2,466 Black/admixed ancestry individuals NA Illumina [141374] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177534 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2577) 2,466 Black/admixed ancestry individuals NA Illumina [160864] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177535 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2586) 2,466 Black/admixed ancestry individuals NA Illumina [154067] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177536 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2586) 2,466 Black/admixed ancestry individuals NA Illumina [151907] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179043 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2657) 2,466 Black/admixed ancestry individuals NA Illumina [152223] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177547 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2657) 2,466 Black/admixed ancestry individuals NA Illumina [155535] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178843 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2662) 2,466 Black/admixed ancestry individuals NA Illumina [156481] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177548 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2668) 2,466 Black/admixed ancestry individuals NA Illumina [156144] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177549 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2689) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154997] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177550 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI269) 2,466 Black/admixed ancestry individuals NA Illumina [152474] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177551 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2691) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161930] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177552 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2482) 2,466 Black/admixed ancestry individuals NA Illumina [153546] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177516 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI250) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156827] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177519 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2511) 2,466 Black/admixed ancestry individuals NA Illumina [154966] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177523 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2522) 2,466 Black/admixed ancestry individuals NA Illumina [152036] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177525 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2526) 2,466 Black/admixed ancestry individuals NA Illumina [151989] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177526 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI254) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159313] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177528 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Xanthosine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151360] 1 xanthosine measurement http://www.ebi.ac.uk/efo/EFO_0010549 GCST90176084 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Xanthurenic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [164290] 0 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90176085 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2474) 2,466 Black/admixed ancestry individuals NA Illumina [144683] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177512 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2474) 2,466 Black/admixed ancestry individuals NA Illumina [169015] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179042 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2477) 2,466 Black/admixed ancestry individuals NA Illumina [141357] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177513 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2477) 2,466 Black/admixed ancestry individuals NA Illumina [156679] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178839 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2479) 2,466 Black/admixed ancestry individuals NA Illumina [149488] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177514 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI248) 2,466 Black/admixed ancestry individuals NA Illumina [147548] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177515 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI249) 2,466 Black/admixed ancestry individuals NA Illumina [159698] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177517 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI249) 2,466 Black/admixed ancestry individuals NA Illumina [160157] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178840 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2492) 2,466 Black/admixed ancestry individuals NA Illumina [154779] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177518 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2508) 2,466 Black/admixed ancestry individuals NA Illumina [147223] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177520 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2509) 2,466 Black/admixed ancestry individuals NA Illumina [154989] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177521 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI251) 2,466 Black/admixed ancestry individuals NA Illumina [148778] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177522 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2514) 2,466 Black/admixed ancestry individuals NA Illumina [151734] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177524 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2532) 2,466 Black/admixed ancestry individuals NA Illumina [154869] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177527 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2542) 2,466 Black/admixed ancestry individuals NA Illumina [151025] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177529 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2542) 2,466 Black/admixed ancestry individuals NA Illumina [153141] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178841 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2551) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163820] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177530 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Threonine levels 2,466 Black/admixed ancestry individuals NA Illumina [155404] 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90178699 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Thyroxine levels 2,466 Black/admixed ancestry individuals NA Illumina [154398] 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90178700 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Trigonelline levels 2,466 Black/admixed ancestry individuals NA Illumina [149872] 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90178701 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Trimethylamine n-oxide levels 2,466 Black/admixed ancestry individuals NA Illumina [167539] 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90178702 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Trimethylbenzene levels 2,466 Black/admixed ancestry individuals NA Illumina [158550] 0 trimethylbenzene measurement http://www.ebi.ac.uk/efo/EFO_0801221 GCST90178703 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Tryptophan levels 2,466 Black/admixed ancestry individuals NA Illumina [151437] 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90178704 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Tyrosine levels 2,466 Black/admixed ancestry individuals NA Illumina [152084] 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90178705 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. UDP-GlcNAc levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150132] 1 UDP-GlcNAc measurement http://www.ebi.ac.uk/efo/EFO_0801222 GCST90176079 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Uracil levels 2,466 Black/admixed ancestry individuals NA Illumina [146590] 0 uracil measurement http://www.ebi.ac.uk/efo/EFO_0800644 GCST90176080 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Urate levels 2,466 Black/admixed ancestry individuals NA Illumina [161669] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90178706 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Uric acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161234] 2 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90176081 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Uridine levels 2,466 Black/admixed ancestry individuals NA Illumina [157370] 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90176082 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Urobilinogen levels 2,466 Black/admixed ancestry individuals NA Illumina [150128] 0 I-urobilinogen measurement http://www.ebi.ac.uk/efo/EFO_0800155 GCST90178707 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Urobilinogen levels 2,466 Black/admixed ancestry individuals NA Illumina [147937] 0 I-urobilinogen measurement http://www.ebi.ac.uk/efo/EFO_0800155 GCST90178916 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Urocanic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162954] 1 Urocanic acid (RG) measurement http://www.ebi.ac.uk/efo/EFO_0021676 GCST90178708 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Valine levels 2,466 Black/admixed ancestry individuals NA Illumina [150703] 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90178709 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Valine-d8 levels 2,466 Black/admixed ancestry individuals NA Illumina [154031] 0 valine-d8 measurement http://www.ebi.ac.uk/efo/EFO_0801223 GCST90178710 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Valsartan levels 2,466 Black/admixed ancestry individuals NA Illumina [155785] 0 valsartan measurement http://www.ebi.ac.uk/efo/EFO_0801224 GCST90178711 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Valsartan levels 2,466 Black/admixed ancestry individuals NA Illumina [139880] 0 valsartan measurement http://www.ebi.ac.uk/efo/EFO_0801224 GCST90179104 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Verapamil levels 2,466 Black/admixed ancestry individuals NA Illumina [174290] 0 verapamil measurement http://www.ebi.ac.uk/efo/EFO_0801225 GCST90179105 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI176) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157275] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178712 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Warfarin levels 2,466 Black/admixed ancestry individuals NA Illumina [152226] 0 warfarin measurement http://www.ebi.ac.uk/efo/EFO_0801226 GCST90176106 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Warfarin levels 2,466 Black/admixed ancestry individuals NA Illumina [217252] 0 warfarin measurement http://www.ebi.ac.uk/efo/EFO_0801226 GCST90179106 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Xanthine levels 2,466 Black/admixed ancestry individuals NA Illumina [166359] 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90176083 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Xanthine levels 2,466 Black/admixed ancestry individuals NA Illumina [158371] 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90178713 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2694) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154080] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177553 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2698) 2,466 Black/admixed ancestry individuals NA Illumina [160763] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177554 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2698) 2,466 Black/admixed ancestry individuals NA Illumina [158259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179044 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI27) 2,466 Black/admixed ancestry individuals NA Illumina [157804] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177555 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI270) 2,466 Black/admixed ancestry individuals NA Illumina [151588] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177556 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2714) 2,466 Black/admixed ancestry individuals NA Illumina [141320] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177557 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2718) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162018] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177558 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2727) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155493] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177559 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI273) 2,466 Black/admixed ancestry individuals NA Illumina [166787] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177560 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI273) 2,466 Black/admixed ancestry individuals NA Illumina [149113] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178844 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2735) 2,466 Black/admixed ancestry individuals NA Illumina [150142] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177561 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2753) 2,466 Black/admixed ancestry individuals NA Illumina [147508] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177562 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2757) 2,466 Black/admixed ancestry individuals NA Illumina [168632] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177563 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2757) 2,466 Black/admixed ancestry individuals NA Illumina [153090] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178845 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2760) 2,466 Black/admixed ancestry individuals NA Illumina [158633] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177564 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2760) 2,466 Black/admixed ancestry individuals NA Illumina [168706] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178846 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2790) 2,466 Black/admixed ancestry individuals NA Illumina [149335] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177565 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2792) 2,466 Black/admixed ancestry individuals NA Illumina [158388] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177566 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2796) 2,466 Black/admixed ancestry individuals NA Illumina [160315] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177567 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2799) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160317] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177568 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI280) 2,466 Black/admixed ancestry individuals NA Illumina [156907] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177569 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2815) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158822] 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177570 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2827) 2,466 Black/admixed ancestry individuals NA Illumina [156909] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177571 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2845) 2,466 Black/admixed ancestry individuals NA Illumina [152033] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177572 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2847) 2,466 Black/admixed ancestry individuals NA Illumina [167184] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177573 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2847) 2,466 Black/admixed ancestry individuals NA Illumina [166101] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178847 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2877) 2,466 Black/admixed ancestry individuals NA Illumina [161425] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177574 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2885) 2,466 Black/admixed ancestry individuals NA Illumina [149177] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177575 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2899) 2,466 Black/admixed ancestry individuals NA Illumina [152818] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177576 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2914) 2,466 Black/admixed ancestry individuals NA Illumina [150042] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177577 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI292) 2,466 Black/admixed ancestry individuals NA Illumina [145022] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177578 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2923) 2,466 Black/admixed ancestry individuals NA Illumina [148763] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177579 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2923) 2,466 Black/admixed ancestry individuals NA Illumina [168562] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178848 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI293) 2,466 Black/admixed ancestry individuals NA Illumina [153444] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177580 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2940) 2,466 Black/admixed ancestry individuals NA Illumina [151165] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177581 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI296) 2,466 Black/admixed ancestry individuals NA Illumina [169585] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177582 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI296) 2,466 Black/admixed ancestry individuals NA Illumina [153698] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178849 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2974) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152676] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177583 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI298) 2,466 Black/admixed ancestry individuals NA Illumina [154046] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177584 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI299) 2,466 Black/admixed ancestry individuals NA Illumina [158612] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177585 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI300) 2,466 Black/admixed ancestry individuals NA Illumina [152435] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177586 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3018) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153703] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177587 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3021) 2,466 Black/admixed ancestry individuals NA Illumina [155685] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177588 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3038) 2,466 Black/admixed ancestry individuals NA Illumina [197632] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179045 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI305) 2,466 Black/admixed ancestry individuals NA Illumina [163469] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177589 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI306) 2,466 Black/admixed ancestry individuals NA Illumina [151526] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177590 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3060) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160332] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177591 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3067) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154951] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177592 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI307) 2,466 Black/admixed ancestry individuals NA Illumina [157224] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177593 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI307) 2,466 Black/admixed ancestry individuals NA Illumina [162921] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178850 Genome-wide sequencing 2022-10-07 34465742 Li Y 2021-08-31 Cell Discov www.ncbi.nlm.nih.gov/pubmed/34465742 Genome-wide association study of COVID-19 severity among the Chinese population. Severe COVID-19 disease 863 Chinese ancestry severe/critical cases, 529 Chinese ancestry mild/moderate controls 43 East Asian ancestry severe/critical cases, 127 East Asian ancestry mild/moderate controls, 862 East Asian ancestry naïve controls, 386 East Asian or South Asian critically ill cases, 1,930 East Asian or South Asian naïve controls Affymetrix [8227125] (imputed) 2 COVID-19 symptoms measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0600019, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90038450 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Hip circumference 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 3 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90134425 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Body mass index 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90134424 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Waist circumference 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 1 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90134426 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Waist-hip ratio 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 8 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90134427 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Longitudinal body mass index 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 2 longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0005937 GCST90134428 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Longitudinal hip circumference 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 0 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90134429 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Longitudinal waist circumference 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90134430 Genome-wide genotyping array 2022-09-07 35794696 Chung W 2022-06-30 Genomics Inform www.ncbi.nlm.nih.gov/pubmed/35794696 Bayesian analysis of longitudinal traits in the Korea Association Resource (KARE) cohort. Longitudinal waist-hip ratio 4,621 East Asian ancestry individuals NA Affymetrix [3848960] (imputed) 2 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90134431 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3074) 2,466 Black/admixed ancestry individuals NA Illumina [152418] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177594 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI308) 2,466 Black/admixed ancestry individuals NA Illumina [156059] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177595 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3105) 2,466 Black/admixed ancestry individuals NA Illumina [166787] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177596 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3105) 2,466 Black/admixed ancestry individuals NA Illumina [164942] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178851 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3107) 2,466 Black/admixed ancestry individuals NA Illumina [148642] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177597 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3125) 2,466 Black/admixed ancestry individuals NA Illumina [143975] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177598 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3125) 2,466 Black/admixed ancestry individuals NA Illumina [144751] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179046 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3127) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154933] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177599 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3131) 2,466 Black/admixed ancestry individuals NA Illumina [155473] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177600 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3139) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159640] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177601 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3143) 2,466 Black/admixed ancestry individuals NA Illumina [156136] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177602 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI315) 2,466 Black/admixed ancestry individuals NA Illumina [153770] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179047 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI317) 2,466 Black/admixed ancestry individuals NA Illumina [154984] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177603 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI317) 2,466 Black/admixed ancestry individuals NA Illumina [154682] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178852 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3172) 2,466 Black/admixed ancestry individuals NA Illumina [151811] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177604 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3172) 2,466 Black/admixed ancestry individuals NA Illumina [150855] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178853 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3176) 2,466 Black/admixed ancestry individuals NA Illumina [156150] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177605 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3179) 2,466 Black/admixed ancestry individuals NA Illumina [152456] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177606 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3190) 2,466 Black/admixed ancestry individuals NA Illumina [158983] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177607 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3204) 2,466 Black/admixed ancestry individuals NA Illumina [135341] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177608 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3223) 2,466 Black/admixed ancestry individuals NA Illumina [144190] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177609 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI324) 2,466 Black/admixed ancestry individuals NA Illumina [166023] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179048 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3247) 2,466 Black/admixed ancestry individuals NA Illumina [159100] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177610 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI325) 2,466 Black/admixed ancestry individuals NA Illumina [148485] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177611 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3251) 2,466 Black/admixed ancestry individuals NA Illumina [164965] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177612 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3426) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151606] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177634 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3436) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152906] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177635 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3442) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151249] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177636 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3451) 2,466 Black/admixed ancestry individuals NA Illumina [149644] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177637 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3453) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152014] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177638 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI348) 2,466 Black/admixed ancestry individuals NA Illumina [149722] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177639 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3485) 2,466 Black/admixed ancestry individuals NA Illumina [154393] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177640 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3492) 2,466 Black/admixed ancestry individuals NA Illumina [153887] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177642 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3500) 2,466 Black/admixed ancestry individuals NA Illumina [169428] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177644 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3513) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161346] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177646 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3529) 2,466 Black/admixed ancestry individuals NA Illumina [155606] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177647 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI353) 2,466 Black/admixed ancestry individuals NA Illumina [148165] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177648 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3530) 2,466 Black/admixed ancestry individuals NA Illumina [160449] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177649 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3530) 2,466 Black/admixed ancestry individuals NA Illumina [145592] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179050 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI354) 2,466 Black/admixed ancestry individuals NA Illumina [152770] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177650 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3557) 2,466 Black/admixed ancestry individuals NA Illumina [170506] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177651 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3586) 2,466 Black/admixed ancestry individuals NA Illumina [159005] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177652 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3586) 2,466 Black/admixed ancestry individuals NA Illumina [151451] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179051 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI349) 2,466 Black/admixed ancestry individuals NA Illumina [151861] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177641 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI350) 2,466 Black/admixed ancestry individuals NA Illumina [155025] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177643 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3504) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162202] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177645 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3592) 2,466 Black/admixed ancestry individuals NA Illumina [163242] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177653 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3599) 2,466 Black/admixed ancestry individuals NA Illumina [164161] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177654 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3603) 2,466 Black/admixed ancestry individuals NA Illumina [171183] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177655 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI362) 2,466 Black/admixed ancestry individuals NA Illumina [154030] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177656 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3628) 2,466 Black/admixed ancestry individuals NA Illumina [167960] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177657 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3643) 2,466 Black/admixed ancestry individuals NA Illumina [151249] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177658 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3643) 2,466 Black/admixed ancestry individuals NA Illumina [157108] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178857 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3684) 2,466 Black/admixed ancestry individuals NA Illumina [156342] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177659 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3685) 2,466 Black/admixed ancestry individuals NA Illumina [163626] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177660 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3688) 2,466 Black/admixed ancestry individuals NA Illumina [168029] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177661 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3697) 2,466 Black/admixed ancestry individuals NA Illumina [148697] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177662 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3697) 2,466 Black/admixed ancestry individuals NA Illumina [135976] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179052 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI370) 2,466 Black/admixed ancestry individuals NA Illumina [156822] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177663 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3704) 2,466 Black/admixed ancestry individuals NA Illumina [156059] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177664 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI371) 2,466 Black/admixed ancestry individuals NA Illumina [156758] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177665 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3710) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149916] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177666 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI372) 2,466 Black/admixed ancestry individuals NA Illumina [153809] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177667 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3722) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152477] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177668 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3723) 2,466 Black/admixed ancestry individuals NA Illumina [151246] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177669 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3724) 2,466 Black/admixed ancestry individuals NA Illumina [167964] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177670 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3725) 2,466 Black/admixed ancestry individuals NA Illumina [151436] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177671 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3726) 2,466 Black/admixed ancestry individuals NA Illumina [162715] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177672 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3727) 2,466 Black/admixed ancestry individuals NA Illumina [150865] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177673 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3727) 2,466 Black/admixed ancestry individuals NA Illumina [150554] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178858 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI373) 2,466 Black/admixed ancestry individuals NA Illumina [157243] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177674 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI374) 2,466 Black/admixed ancestry individuals NA Illumina [154807] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177675 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3745) 2,466 Black/admixed ancestry individuals NA Illumina [145105] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177676 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI375) 2,466 Black/admixed ancestry individuals NA Illumina [170259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177677 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3754) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [164105] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177678 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3251) 2,466 Black/admixed ancestry individuals NA Illumina [168493] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178854 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI326) 2,466 Black/admixed ancestry individuals NA Illumina [145328] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177613 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3263) 2,466 Black/admixed ancestry individuals NA Illumina [153302] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177614 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3267) 2,466 Black/admixed ancestry individuals NA Illumina [140516] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177615 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3269) 2,466 Black/admixed ancestry individuals NA Illumina [157728] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177616 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3269) 2,466 Black/admixed ancestry individuals NA Illumina [149725] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179049 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI327) 2,466 Black/admixed ancestry individuals NA Illumina [157019] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177617 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3274) 2,466 Black/admixed ancestry individuals NA Illumina [166045] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177618 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3282) 2,466 Black/admixed ancestry individuals NA Illumina [144642] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177619 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3283) 2,466 Black/admixed ancestry individuals NA Illumina [146466] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177620 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI329) 2,466 Black/admixed ancestry individuals NA Illumina [153160] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177621 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI329) 2,466 Black/admixed ancestry individuals NA Illumina [162823] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178855 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3303) 2,466 Black/admixed ancestry individuals NA Illumina [150255] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177622 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3303) 2,466 Black/admixed ancestry individuals NA Illumina [150714] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178856 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI332) 2,466 Black/admixed ancestry individuals NA Illumina [153766] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177623 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI333) 2,466 Black/admixed ancestry individuals NA Illumina [154737] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177624 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3334) 2,466 Black/admixed ancestry individuals NA Illumina [142442] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177625 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3344) 2,466 Black/admixed ancestry individuals NA Illumina [152825] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177626 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3348) 2,466 Black/admixed ancestry individuals NA Illumina [152564] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177627 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3368) 2,466 Black/admixed ancestry individuals NA Illumina [162552] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177628 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3369) 2,466 Black/admixed ancestry individuals NA Illumina [170452] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177629 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3370) 2,466 Black/admixed ancestry individuals NA Illumina [167361] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177630 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI338) 2,466 Black/admixed ancestry individuals NA Illumina [155529] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177631 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI339) 2,466 Black/admixed ancestry individuals NA Illumina [156992] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177632 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3403) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155206] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177633 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI376) 2,466 Black/admixed ancestry individuals NA Illumina [152946] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177679 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3769) 2,466 Black/admixed ancestry individuals NA Illumina [157343] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177680 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI377) 2,466 Black/admixed ancestry individuals NA Illumina [155593] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177681 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3770) 2,466 Black/admixed ancestry individuals NA Illumina [160912] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177682 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3774) 2,466 Black/admixed ancestry individuals NA Illumina [159385] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177683 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3776) 2,466 Black/admixed ancestry individuals NA Illumina [159371] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177684 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3778) 2,466 Black/admixed ancestry individuals NA Illumina [152615] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179053 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI378) 2,466 Black/admixed ancestry individuals NA Illumina [152690] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177685 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3783) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160163] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177686 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3784) 2,466 Black/admixed ancestry individuals NA Illumina [159157] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177687 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3785) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159814] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177688 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3788) 2,466 Black/admixed ancestry individuals NA Illumina [148812] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177689 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3788) 2,466 Black/admixed ancestry individuals NA Illumina [159328] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179054 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3792) 2,466 Black/admixed ancestry individuals NA Illumina [160916] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177690 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3800) 2,466 Black/admixed ancestry individuals NA Illumina [163513] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177691 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3801) 2,466 Black/admixed ancestry individuals NA Illumina [157628] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177692 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3808) 2,466 Black/admixed ancestry individuals NA Illumina [151838] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177693 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3810) 2,466 Black/admixed ancestry individuals NA Illumina [160605] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177694 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3819) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161911] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177695 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3869) 2,466 Black/admixed ancestry individuals NA Illumina [170129] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177696 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3870) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150652] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177697 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3876) 2,466 Black/admixed ancestry individuals NA Illumina [152583] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177698 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3877) 2,466 Black/admixed ancestry individuals NA Illumina [152493] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177699 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3888) 2,466 Black/admixed ancestry individuals NA Illumina [158256] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177700 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI389) 2,466 Black/admixed ancestry individuals NA Illumina [155109] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177701 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI404) 2,466 Black/admixed ancestry individuals NA Illumina [157506] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177725 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4043) 2,466 Black/admixed ancestry individuals NA Illumina [153431] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177726 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4060) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154214] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177727 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4065) 2,466 Black/admixed ancestry individuals NA Illumina [155492] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177728 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4066) 2,466 Black/admixed ancestry individuals NA Illumina [147927] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177729 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4067) 2,466 Black/admixed ancestry individuals NA Illumina [151129] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177730 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4068) 2,466 Black/admixed ancestry individuals NA Illumina [155048] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177731 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4070) 2,466 Black/admixed ancestry individuals NA Illumina [151974] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177732 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4076) 2,466 Black/admixed ancestry individuals NA Illumina [152423] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177733 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4077) 2,466 Black/admixed ancestry individuals NA Illumina [176418] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177734 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI408) 2,466 Black/admixed ancestry individuals NA Illumina [153330] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177735 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4080) 2,466 Black/admixed ancestry individuals NA Illumina [152570] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177736 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI409) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157290] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177737 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI411) 2,466 Black/admixed ancestry individuals NA Illumina [152328] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177738 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4123) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157662] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177739 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI413) 2,466 Black/admixed ancestry individuals NA Illumina [167722] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177740 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4130) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150444] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177741 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI414) 2,466 Black/admixed ancestry individuals NA Illumina [163841] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177742 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4144) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155264] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177743 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI415) 2,466 Black/admixed ancestry individuals NA Illumina [153676] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177744 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI416) 2,466 Black/admixed ancestry individuals NA Illumina [154000] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177745 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4169) 2,466 Black/admixed ancestry individuals NA Illumina [157524] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177746 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4169) 2,466 Black/admixed ancestry individuals NA Illumina [160865] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179056 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4175) 2,466 Black/admixed ancestry individuals NA Illumina [157367] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177747 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4201) 2,466 Black/admixed ancestry individuals NA Illumina [149487] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177748 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3893) 2,466 Black/admixed ancestry individuals NA Illumina [153829] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177702 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3893) 2,466 Black/admixed ancestry individuals NA Illumina [154158] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178859 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI390) 2,466 Black/admixed ancestry individuals NA Illumina [153736] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177703 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI391) 2,466 Black/admixed ancestry individuals NA Illumina [158018] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177704 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI392) 2,466 Black/admixed ancestry individuals NA Illumina [156626] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177705 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI393) 2,466 Black/admixed ancestry individuals NA Illumina [156995] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177706 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI394) 2,466 Black/admixed ancestry individuals NA Illumina [158039] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177707 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3948) 2,466 Black/admixed ancestry individuals NA Illumina [157955] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177708 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI395) 2,466 Black/admixed ancestry individuals NA Illumina [154420] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177709 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3977) 2,466 Black/admixed ancestry individuals NA Illumina [157668] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177710 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI398) 2,466 Black/admixed ancestry individuals NA Illumina [156249] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177711 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3998) 2,466 Black/admixed ancestry individuals NA Illumina [155024] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177712 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3999) 2,466 Black/admixed ancestry individuals NA Illumina [152735] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177713 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4) 2,466 Black/admixed ancestry individuals NA Illumina [146954] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177714 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4) 2,466 Black/admixed ancestry individuals NA Illumina [157291] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179055 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI400) 2,466 Black/admixed ancestry individuals NA Illumina [156733] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177715 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4001) 2,466 Black/admixed ancestry individuals NA Illumina [155702] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177716 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4005) 2,466 Black/admixed ancestry individuals NA Illumina [158526] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177717 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4009) 2,466 Black/admixed ancestry individuals NA Illumina [158404] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177718 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI401) 2,466 Black/admixed ancestry individuals NA Illumina [154529] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177719 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI402) 2,466 Black/admixed ancestry individuals NA Illumina [152894] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177720 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4024) 2,466 Black/admixed ancestry individuals NA Illumina [169497] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177721 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4027) 2,466 Black/admixed ancestry individuals NA Illumina [173099] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177722 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4032) 2,466 Black/admixed ancestry individuals NA Illumina [155869] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177723 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4039) 2,466 Black/admixed ancestry individuals NA Illumina [167909] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177724 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4201) 2,466 Black/admixed ancestry individuals NA Illumina [150672] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178860 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4204) 2,466 Black/admixed ancestry individuals NA Illumina [156885] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177749 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4204) 2,466 Black/admixed ancestry individuals NA Illumina [141474] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179057 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI422) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151555] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177750 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI423) 2,466 Black/admixed ancestry individuals NA Illumina [159335] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177751 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI424) 2,466 Black/admixed ancestry individuals NA Illumina [155557] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177752 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4246) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157526] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177753 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4247) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157280] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177754 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI425) 2,466 Black/admixed ancestry individuals NA Illumina [153472] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177755 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4251) 2,466 Black/admixed ancestry individuals NA Illumina [168053] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177756 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4251) 2,466 Black/admixed ancestry individuals NA Illumina [179831] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178861 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI426) 2,466 Black/admixed ancestry individuals NA Illumina [158268] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177757 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI427) 2,466 Black/admixed ancestry individuals NA Illumina [149809] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177758 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4272) 2,466 Black/admixed ancestry individuals NA Illumina [142523] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177759 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4272) 2,466 Black/admixed ancestry individuals NA Illumina [154882] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178862 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI428) 2,466 Black/admixed ancestry individuals NA Illumina [151425] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177760 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4288) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154661] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177761 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI429) 2,466 Black/admixed ancestry individuals NA Illumina [159809] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177762 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4296) 2,466 Black/admixed ancestry individuals NA Illumina [155223] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177763 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI430) 2,466 Black/admixed ancestry individuals NA Illumina [152871] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177764 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4307) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153710] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177765 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI431) 2,466 Black/admixed ancestry individuals NA Illumina [144183] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177766 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4319) 2,466 Black/admixed ancestry individuals NA Illumina [154504] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177767 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4320) 2,466 Black/admixed ancestry individuals NA Illumina [154107] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177768 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI433) 2,466 Black/admixed ancestry individuals NA Illumina [146769] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177769 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4550) 2,466 Black/admixed ancestry individuals NA Illumina [154317] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177791 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI456) 2,466 Black/admixed ancestry individuals NA Illumina [159432] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177792 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4560) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [146886] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177793 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4567) 2,466 Black/admixed ancestry individuals NA Illumina [151081] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177794 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4567) 2,466 Black/admixed ancestry individuals NA Illumina [142852] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179058 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4569) 2,466 Black/admixed ancestry individuals NA Illumina [151328] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177795 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI457) 2,466 Black/admixed ancestry individuals NA Illumina [151691] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177796 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4574) 2,466 Black/admixed ancestry individuals NA Illumina [158664] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177797 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI458) 2,466 Black/admixed ancestry individuals NA Illumina [142653] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177798 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4583) 2,466 Black/admixed ancestry individuals NA Illumina [184537] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179059 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4584) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [170306] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177799 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4587) 2,466 Black/admixed ancestry individuals NA Illumina [156028] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177800 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4587) 2,466 Black/admixed ancestry individuals NA Illumina [151483] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179060 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4596) 2,466 Black/admixed ancestry individuals NA Illumina [166733] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177801 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4598) 2,466 Black/admixed ancestry individuals NA Illumina [164300] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177802 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4604) 2,466 Black/admixed ancestry individuals NA Illumina [153534] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177803 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4604) 2,466 Black/admixed ancestry individuals NA Illumina [159033] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179061 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4605) 2,466 Black/admixed ancestry individuals NA Illumina [164080] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177804 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4606) 2,466 Black/admixed ancestry individuals NA Illumina [149908] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177805 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4617) 2,466 Black/admixed ancestry individuals NA Illumina [152928] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177806 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4629) 2,466 Black/admixed ancestry individuals NA Illumina [152946] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177807 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4631) 2,466 Black/admixed ancestry individuals NA Illumina [161757] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177808 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4635) 2,466 Black/admixed ancestry individuals NA Illumina [158493] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177809 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4643) 2,466 Black/admixed ancestry individuals NA Illumina [151613] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179062 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4647) 2,466 Black/admixed ancestry individuals NA Illumina [150842] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177810 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4350) 2,466 Black/admixed ancestry individuals NA Illumina [165209] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177770 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4350) 2,466 Black/admixed ancestry individuals NA Illumina [149756] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178863 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4353) 2,466 Black/admixed ancestry individuals NA Illumina [156021] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177771 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4368) 2,466 Black/admixed ancestry individuals NA Illumina [157139] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177772 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4368) 2,466 Black/admixed ancestry individuals NA Illumina [148043] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178864 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4378) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149843] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177773 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4391) 2,466 Black/admixed ancestry individuals NA Illumina [171621] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177774 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4393) 2,466 Black/admixed ancestry individuals NA Illumina [157734] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177775 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4393) 2,466 Black/admixed ancestry individuals NA Illumina [159197] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178865 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI443) 2,466 Black/admixed ancestry individuals NA Illumina [159667] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177776 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4438) 2,466 Black/admixed ancestry individuals NA Illumina [181478] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177777 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4439) 2,466 Black/admixed ancestry individuals NA Illumina [149442] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177778 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI444) 2,466 Black/admixed ancestry individuals NA Illumina [141438] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177779 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4444) 2,466 Black/admixed ancestry individuals NA Illumina [165183] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177780 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI445) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156475] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177781 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI446) 2,466 Black/admixed ancestry individuals NA Illumina [150003] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177782 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4473) 2,466 Black/admixed ancestry individuals NA Illumina [150295] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177783 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4474) 2,466 Black/admixed ancestry individuals NA Illumina [164974] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177784 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI448) 2,466 Black/admixed ancestry individuals NA Illumina [153423] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177785 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI450) 2,466 Black/admixed ancestry individuals NA Illumina [147750] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177786 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4508) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154048] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177787 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4545) 2,466 Black/admixed ancestry individuals NA Illumina [170173] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177788 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4546) 2,466 Black/admixed ancestry individuals NA Illumina [167643] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177789 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4546) 2,466 Black/admixed ancestry individuals NA Illumina [154579] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178866 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI455) 2,466 Black/admixed ancestry individuals NA Illumina [154682] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177790 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4657) 2,466 Black/admixed ancestry individuals NA Illumina [160889] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177811 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4657) 2,466 Black/admixed ancestry individuals NA Illumina [146761] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178867 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4658) 2,466 Black/admixed ancestry individuals NA Illumina [146760] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177812 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4666) 2,466 Black/admixed ancestry individuals NA Illumina [158971] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177813 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4666) 2,466 Black/admixed ancestry individuals NA Illumina [154914] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178868 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4667) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153253] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177814 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI467) 2,466 Black/admixed ancestry individuals NA Illumina [151278] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177815 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4678) 2,466 Black/admixed ancestry individuals NA Illumina [148744] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177816 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4680) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152113] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177817 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4683) 2,466 Black/admixed ancestry individuals NA Illumina [146818] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177818 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4687) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154907] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177819 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4689) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163837] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177820 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4690) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150681] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177821 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4708) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153114] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177822 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4755) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156726] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177823 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI477) 2,466 Black/admixed ancestry individuals NA Illumina [158321] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177824 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4773) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155628] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177825 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4775) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155469] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177826 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI478) 2,466 Black/admixed ancestry individuals NA Illumina [150132] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177827 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4784) 2,466 Black/admixed ancestry individuals NA Illumina [239793] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179063 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI479) 2,466 Black/admixed ancestry individuals NA Illumina [155185] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177828 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI480) 2,466 Black/admixed ancestry individuals NA Illumina [158820] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177829 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI480) 2,466 Black/admixed ancestry individuals NA Illumina [153715] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178869 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4800) 2,466 Black/admixed ancestry individuals NA Illumina [161318] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177830 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4805) 2,466 Black/admixed ancestry individuals NA Illumina [155690] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177831 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5024) 2,466 Black/admixed ancestry individuals NA Illumina [151608] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177852 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI503) 2,466 Black/admixed ancestry individuals NA Illumina [149259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177853 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI503) 2,466 Black/admixed ancestry individuals NA Illumina [147937] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178874 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5054) 2,466 Black/admixed ancestry individuals NA Illumina [152634] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177854 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5056) 2,466 Black/admixed ancestry individuals NA Illumina [149360] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177855 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5072) 2,466 Black/admixed ancestry individuals NA Illumina [150403] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177856 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5072) 2,466 Black/admixed ancestry individuals NA Illumina [149211] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178875 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5083) 2,466 Black/admixed ancestry individuals NA Illumina [163592] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177857 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI509) 2,466 Black/admixed ancestry individuals NA Illumina [156519] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177858 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5099) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158602] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177859 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI510) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152055] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177860 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5101) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150357] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177861 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI511) 2,466 Black/admixed ancestry individuals NA Illumina [145995] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177862 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI512) 2,466 Black/admixed ancestry individuals NA Illumina [158958] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177863 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI513) 2,466 Black/admixed ancestry individuals NA Illumina [158864] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177864 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5153) 2,466 Black/admixed ancestry individuals NA Illumina [143829] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177865 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5165) 2,466 Black/admixed ancestry individuals NA Illumina [163257] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177866 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5169) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161248] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177867 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5171) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [171156] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177868 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5202) 2,466 Black/admixed ancestry individuals NA Illumina [152290] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177869 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5224) 2,466 Black/admixed ancestry individuals NA Illumina [164280] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177870 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5228) 2,466 Black/admixed ancestry individuals NA Illumina [164970] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177871 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5229) 2,466 Black/admixed ancestry individuals NA Illumina [154220] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177872 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI523) 2,466 Black/admixed ancestry individuals NA Illumina [166044] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177873 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5230) 2,466 Black/admixed ancestry individuals NA Illumina [144646] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177874 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI481) 2,466 Black/admixed ancestry individuals NA Illumina [147208] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177832 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4811) 2,466 Black/admixed ancestry individuals NA Illumina [152485] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177833 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4811) 2,466 Black/admixed ancestry individuals NA Illumina [146579] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179064 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4849) 2,466 Black/admixed ancestry individuals NA Illumina [152249] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177834 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4851) 2,466 Black/admixed ancestry individuals NA Illumina [152452] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177835 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4851) 2,466 Black/admixed ancestry individuals NA Illumina [152770] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178870 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI488) 2,466 Black/admixed ancestry individuals NA Illumina [149025] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177836 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4887) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154859] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177837 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI489) 2,466 Black/admixed ancestry individuals NA Illumina [153444] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177838 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI490) 2,466 Black/admixed ancestry individuals NA Illumina [155007] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177839 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4907) 2,466 Black/admixed ancestry individuals NA Illumina [153084] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177840 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4921) 2,466 Black/admixed ancestry individuals NA Illumina [154953] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177841 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4949) 2,466 Black/admixed ancestry individuals NA Illumina [149435] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177842 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4952) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150067] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177843 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4953) 2,466 Black/admixed ancestry individuals NA Illumina [150835] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177844 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4953) 2,466 Black/admixed ancestry individuals NA Illumina [150229] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178871 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4955) 2,466 Black/admixed ancestry individuals NA Illumina [152296] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177845 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4955) 2,466 Black/admixed ancestry individuals NA Illumina [149798] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178872 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4968) 2,466 Black/admixed ancestry individuals NA Illumina [150441] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177846 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4970) 2,466 Black/admixed ancestry individuals NA Illumina [152038] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177847 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4974) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153626] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177848 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4979) 2,466 Black/admixed ancestry individuals NA Illumina [165979] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177849 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI4982) 2,466 Black/admixed ancestry individuals NA Illumina [153928] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177850 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5019) 2,466 Black/admixed ancestry individuals NA Illumina [152042] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177851 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5019) 2,466 Black/admixed ancestry individuals NA Illumina [151837] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178873 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5230) 2,466 Black/admixed ancestry individuals NA Illumina [151792] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179065 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5235) 2,466 Black/admixed ancestry individuals NA Illumina [146206] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177875 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5236) 2,466 Black/admixed ancestry individuals NA Illumina [174189] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177876 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5236) 2,466 Black/admixed ancestry individuals NA Illumina [152286] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179066 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI524) 2,466 Black/admixed ancestry individuals NA Illumina [152521] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177877 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5241) 2,466 Black/admixed ancestry individuals NA Illumina [134235] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177878 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5250) 2,466 Black/admixed ancestry individuals NA Illumina [153706] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177879 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5250) 2,466 Black/admixed ancestry individuals NA Illumina [174827] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178876 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI526) 2,466 Black/admixed ancestry individuals NA Illumina [165217] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177880 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5294) 2,466 Black/admixed ancestry individuals NA Illumina [140863] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177881 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI530) 2,466 Black/admixed ancestry individuals NA Illumina [158233] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177882 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5321) 2,466 Black/admixed ancestry individuals NA Illumina [152175] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177883 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5321) 2,466 Black/admixed ancestry individuals NA Illumina [137381] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179067 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5325) 2,466 Black/admixed ancestry individuals NA Illumina [159539] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177884 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI534) 2,466 Black/admixed ancestry individuals NA Illumina [154552] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177885 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI536) 2,466 Black/admixed ancestry individuals NA Illumina [153525] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177886 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5365) 2,466 Black/admixed ancestry individuals NA Illumina [133751] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177887 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5380) 2,466 Black/admixed ancestry individuals NA Illumina [165127] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177888 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5380) 2,466 Black/admixed ancestry individuals NA Illumina [176173] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179068 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5386) 2,466 Black/admixed ancestry individuals NA Illumina [177508] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177889 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI539) 2,466 Black/admixed ancestry individuals NA Illumina [144003] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177890 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5420) 2,466 Black/admixed ancestry individuals NA Illumina [162891] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177891 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5420) 2,466 Black/admixed ancestry individuals NA Illumina [148827] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179069 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5430) 2,466 Black/admixed ancestry individuals NA Illumina [137348] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177892 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI546) 2,466 Black/admixed ancestry individuals NA Illumina [165006] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177893 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5604) 2,466 Black/admixed ancestry individuals NA Illumina [152976] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178877 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5607) 2,466 Black/admixed ancestry individuals NA Illumina [152170] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177916 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI561) 2,466 Black/admixed ancestry individuals NA Illumina [160838] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177917 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5616) 2,466 Black/admixed ancestry individuals NA Illumina [146416] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177918 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5616) 2,466 Black/admixed ancestry individuals NA Illumina [152769] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179073 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI562) 2,466 Black/admixed ancestry individuals NA Illumina [152415] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177919 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5622) 2,466 Black/admixed ancestry individuals NA Illumina [162577] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177920 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI563) 2,466 Black/admixed ancestry individuals NA Illumina [156395] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177921 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5631) 2,466 Black/admixed ancestry individuals NA Illumina [157903] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177922 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI564) 2,466 Black/admixed ancestry individuals NA Illumina [153410] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177923 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5641) 2,466 Black/admixed ancestry individuals NA Illumina [159670] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177924 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5648) 2,466 Black/admixed ancestry individuals NA Illumina [161206] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177925 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI565) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156979] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177926 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI566) 2,466 Black/admixed ancestry individuals NA Illumina [153715] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177927 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5664) 2,466 Black/admixed ancestry individuals NA Illumina [162517] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177928 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5665) 2,466 Black/admixed ancestry individuals NA Illumina [151670] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177929 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5666) 2,466 Black/admixed ancestry individuals NA Illumina [139287] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179074 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI567) 2,466 Black/admixed ancestry individuals NA Illumina [153432] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177930 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5672) 2,466 Black/admixed ancestry individuals NA Illumina [162603] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177931 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5672) 2,466 Black/admixed ancestry individuals NA Illumina [146259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179075 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI568) 2,466 Black/admixed ancestry individuals NA Illumina [158100] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177932 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5681) 2,466 Black/admixed ancestry individuals NA Illumina [207852] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179076 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5684) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162438] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177933 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI569) 2,466 Black/admixed ancestry individuals NA Illumina [150144] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177934 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5705) 2,466 Black/admixed ancestry individuals NA Illumina [140993] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177935 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI584) 2,466 Black/admixed ancestry individuals NA Illumina [153144] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177956 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5840) 2,466 Black/admixed ancestry individuals NA Illumina [159607] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177957 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5842) 2,466 Black/admixed ancestry individuals NA Illumina [155693] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177958 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5843) 2,466 Black/admixed ancestry individuals NA Illumina [153202] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177959 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5843) 2,466 Black/admixed ancestry individuals NA Illumina [145234] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178881 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI585) 2,466 Black/admixed ancestry individuals NA Illumina [154111] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177960 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI586) 2,466 Black/admixed ancestry individuals NA Illumina [154370] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177961 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5868) 2,466 Black/admixed ancestry individuals NA Illumina [148144] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177962 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5868) 2,466 Black/admixed ancestry individuals NA Illumina [146216] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178882 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI587) 2,466 Black/admixed ancestry individuals NA Illumina [153190] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177963 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI588) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152877] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177964 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5884) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159166] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177965 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5888) 2,466 Black/admixed ancestry individuals NA Illumina [166989] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177966 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI589) 2,466 Black/admixed ancestry individuals NA Illumina [154722] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177967 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI590) 2,466 Black/admixed ancestry individuals NA Illumina [152078] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177968 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5900) 2,466 Black/admixed ancestry individuals NA Illumina [165213] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177969 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5900) 2,466 Black/admixed ancestry individuals NA Illumina [144086] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179079 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5904) 2,466 Black/admixed ancestry individuals NA Illumina [153572] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177970 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5908) 2,466 Black/admixed ancestry individuals NA Illumina [154375] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177971 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI591) 2,466 Black/admixed ancestry individuals NA Illumina [155804] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177972 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5917) 2,466 Black/admixed ancestry individuals NA Illumina [163170] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177973 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5917) 2,466 Black/admixed ancestry individuals NA Illumina [161391] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178883 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5920) 2,466 Black/admixed ancestry individuals NA Illumina [165286] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177974 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI593) 2,466 Black/admixed ancestry individuals NA Illumina [154541] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177975 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI594) 2,466 Black/admixed ancestry individuals NA Illumina [154404] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177976 Genome-wide sequencing 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute glomerulonephritis 274 European ancestry cases, 475,255 European ancestry controls, 443 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Affymetrix, Illumina [25844004] (imputed) 1 glomerulonephritis http://purl.obolibrary.org/obo/MONDO_0002462 GCST90018788 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute pancreatitis 3,798 European ancestry cases, 476,104 European ancestry controls, 827 East Asian ancestry cases, 177,471 East Asian ancestry controls NA Affymetrix, Illumina [25843473] (imputed) 3 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90018789 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute renal failure 7,695 European ancestry cases, 474,571 European ancestry controls, 465 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Affymetrix, Illumina [25844422] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90018790 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Allergic conjunctivitis 613 European ancestry cases, 474,657 European ancestry controls, 3,900 East Asian ancestry cases, 174,719 East Asian ancestry controls NA Affymetrix, Illumina [25843839] (imputed) 0 conjunctivitis http://www.ebi.ac.uk/efo/EFO_0009450 GCST90018791 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Allergic rhinitis 4,387 European ancestry cases, 471,273 European ancestry controls, 7,897 East Asian ancestry cases, 153,666 East Asian ancestry controls NA Affymetrix, Illumina [25843170] (imputed) 1 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90018792 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Angina pectoris 30,025 European ancestry cases, 440,906 European ancestry controls, 14,007 East Asian ancestry cases, 145,158 East Asian ancestry controls NA Affymetrix, Illumina [25842036] (imputed) 55 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90018793 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Aplastic anemia 4,128 European ancestry cases, 469,372 European ancestry controls, 53 East Asian ancestry cases, 174,057 East Asian ancestry controls NA Affymetrix, Illumina [25844082] (imputed) 1 Aplastic anemia http://purl.obolibrary.org/obo/HP_0001915 GCST90018794 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Asthma 38,369 European ancestry cases, 411,131 European ancestry controls, 13,015 East Asian ancestry cases, 162,933 East Asian ancestry controls NA Affymetrix, Illumina [25837673] (imputed) 60 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90018795 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Atrial fibrillation/atrial flutter 29,212 European ancestry cases, 400,539 European ancestry controls, 4,150 East Asian ancestry cases, 155,540 East Asian ancestry controls NA Affymetrix, Illumina [25830072] (imputed) 77 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90018796 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Back pain 22,413 European ancestry cases, 445,856 European ancestry controls, 1,732 East Asian ancestry cases, 176,994 East Asian ancestry controls NA Affymetrix, Illumina [25841286] (imputed) 3 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90018797 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Behcet's disease 27 European ancestry cases, 317,225 European ancestry controls, 78 East Asian ancestry cases, 171,966 East Asian ancestry controls NA Affymetrix, Illumina [20455535] (imputed) 0 Behcet's syndrome http://www.ebi.ac.uk/efo/EFO_0003780 GCST90018798 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Breast cancer 17,389 European ancestry cases, 240,341 European ancestry controls, 6,325 East Asian ancestry cases, 73,225 East Asian ancestry controls NA Affymetrix, Illumina [25794640] (imputed) 46 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90018799 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Brain tumor 833 European ancestry cases, 490,709 European ancestry controls, 405 East Asian ancestry cases, 178,321 East Asian ancestry controls NA Affymetrix, Illumina [25845383] (imputed) 2 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90018800 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Bronchiectasis 2,888 European ancestry cases, 440,263 European ancestry controls, 241 East Asian ancestry cases, 161,803 East Asian ancestry controls NA Affymetrix, Illumina [25839694] (imputed) 2 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90018801 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Bronchitis 4,483 European ancestry cases, 474,818 European ancestry controls, 1,465 East Asian ancestry cases, 170,000 East Asian ancestry controls NA Affymetrix, Illumina [25844193] (imputed) 3 bronchitis http://www.ebi.ac.uk/efo/EFO_0009661 GCST90018802 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hepatic bile duct cancer 832 European ancestry cases, 475,259 European ancestry controls, 418 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Affymetrix, Illumina [25843020] (imputed) 1 cholangiocarcinoma http://www.ebi.ac.uk/efo/EFO_0005221 GCST90018803 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic hepatitis B infection 145 European ancestry cases, 351,740 European ancestry controls, 2,234 East Asian ancestry cases, 169,588 East Asian ancestry controls NA Affymetrix, Illumina [20457334] (imputed) 1 chronic hepatitis B virus infection http://www.ebi.ac.uk/efo/EFO_0004239 GCST90018804 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic hepatitis C infection 273 European ancestry cases, 351,740 European ancestry controls, 7,110 East Asian ancestry cases, 169,588 East Asian ancestry controls NA Affymetrix, Illumina [20457788] (imputed) 4 chronic hepatitis C virus infection http://www.ebi.ac.uk/efo/EFO_0004220 GCST90018805 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic heart failure 14,262 European ancestry cases, 471,898 European ancestry controls, 10,540 East Asian ancestry cases, 168,186 East Asian ancestry controls NA Affymetrix, Illumina [25844553] (imputed) 9 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90018806 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic obstructive pulmonary disease 13,530 European ancestry cases, 454,945 European ancestry controls, 4,017 East Asian ancestry cases, 162,653 East Asian ancestry controls NA Affymetrix, Illumina [25843162] (imputed) 13 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90018807 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Colorectal cancer 6,581 European ancestry cases, 463,421 European ancestry controls, 8,305 East Asian ancestry cases, 159,386 East Asian ancestry controls NA Affymetrix, Illumina [25843452] (imputed) 34 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90018808 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic suppurative otitis media 1,108 European ancestry cases, 483,037 European ancestry controls, 2,206 East Asian ancestry cases, 176,520 East Asian ancestry controls NA Affymetrix, Illumina [25844637] (imputed) 0 suppurative otitis media http://www.ebi.ac.uk/efo/EFO_0007503 GCST90018809 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cesarian section 5,336 European ancestry cases, 237,735 European ancestry controls, 451 East Asian ancestry cases, 82,310 East Asian ancestry controls NA Affymetrix, Illumina [25770781] (imputed) 0 cesarean section http://www.ebi.ac.uk/efo/EFO_0009636 GCST90018810 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cardiac valvular disease 25,070 European ancestry cases, 440,457 European ancestry controls, 1,995 East Asian ancestry cases, 176,731 East Asian ancestry controls NA Affymetrix, Illumina [25842568] (imputed) 2 heart valve disease http://www.ebi.ac.uk/efo/EFO_0009551 GCST90018811 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cardiomegaly 3,233 European ancestry cases, 349,893 European ancestry controls, 743 East Asian ancestry cases, 177,983 East Asian ancestry controls NA Affymetrix, Illumina [20458035] (imputed) 0 cardiac hypertrophy http://www.ebi.ac.uk/efo/EFO_0002503 GCST90018812 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (vasodilators used in cardiac diseases) 17,050 East Asian ancestry cases, 161,676 East Asian ancestry controls NA Illumina [13429980] (imputed) 17 Vasodilators used in cardiac diseases use measurement http://www.ebi.ac.uk/efo/EFO_0009926 GCST90018763 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antihypertensives) 5,688 East Asian ancestry cases, 173,038 East Asian ancestry controls NA Illumina [13134967] (imputed) 2 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90018764 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (diuretics) 22,356 East Asian ancestry cases, 156,370 East Asian ancestry controls NA Illumina [13134967] (imputed) 1 Diuretic use measurement http://www.ebi.ac.uk/efo/EFO_0009928 GCST90018765 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (beta blocking agents) 20,367 East Asian ancestry cases, 158,359 East Asian ancestry controls NA Illumina [13134967] (imputed) 8 Beta blocking agent use measurement http://www.ebi.ac.uk/efo/EFO_0009929 GCST90018766 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (calcium channel blockers) 49,327 East Asian ancestry cases, 129,399 East Asian ancestry controls NA Illumina [13134967] (imputed) 22 Calcium channel blocker use measurement http://www.ebi.ac.uk/efo/EFO_0009930 GCST90018767 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (agents acting on the renin-angiotensin system) 45,820 East Asian ancestry cases, 132,906 East Asian ancestry controls NA Illumina [13134967] (imputed) 12 Agents acting on the renin-angiotensin system use measurement http://www.ebi.ac.uk/efo/EFO_0009931 GCST90018768 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (HMG CoA reductase inhibitors) 33,295 East Asian ancestry cases, 145,431 East Asian ancestry controls NA Illumina [13429980] (imputed) 30 HMG CoA reductase inhibitor use measurement http://www.ebi.ac.uk/efo/EFO_0009932 GCST90018769 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (thyroid preparations) 3,103 East Asian ancestry cases, 175,623 East Asian ancestry controls NA Illumina [13429980] (imputed) 2 Thyroid preparation use measurement http://www.ebi.ac.uk/efo/EFO_0009933 GCST90018770 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (immunosuppressants) 3,483 East Asian ancestry cases, 175,243 East Asian ancestry controls NA Illumina [13134967] (imputed) 7 Immunosuppressant use measurement http://www.ebi.ac.uk/efo/EFO_0009934 GCST90018771 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (anti-inflammatory and antirheumatic products, non-steroids) 29,694 East Asian ancestry cases, 149,032 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Non-steroidal anti-inflammatory and antirheumatic product use measurement http://www.ebi.ac.uk/efo/EFO_0009935 GCST90018772 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (drugs affecting bone structure and mineralization) 6,143 East Asian ancestry cases, 172,583 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Drugs affecting bone structure and mineralization use measurement http://www.ebi.ac.uk/efo/EFO_0009936 GCST90018773 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (opioids) 3,566 East Asian ancestry cases, 175,160 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 Opioid use measurement http://www.ebi.ac.uk/efo/EFO_0009937 GCST90018774 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (salicylic acid and derivatives) 41,461 East Asian ancestry cases, 137,265 East Asian ancestry controls NA Illumina [13429980] (imputed) 18 aspirin use measurement http://www.ebi.ac.uk/efo/EFO_0007013 GCST90018775 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (anilides) 4,421 East Asian ancestry cases, 174,305 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 Anilide use measurement http://www.ebi.ac.uk/efo/EFO_0009938 GCST90018776 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antimigraine preparations) 387 East Asian ancestry cases, 178,339 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Antimigraine preparation use measurement http://www.ebi.ac.uk/efo/EFO_0009939 GCST90018777 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antidepressants) 3,288 East Asian ancestry cases, 175,438 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 Antidepressant use measurement http://www.ebi.ac.uk/efo/EFO_0009940 GCST90018778 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (adrenergics, inhalants) 5,880 East Asian ancestry cases, 172,846 East Asian ancestry controls NA Illumina [13429980] (imputed) 2 Inhalant adrenergic use measurement http://www.ebi.ac.uk/efo/EFO_0009941 GCST90018779 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (glucocorticoids) 13,102 East Asian ancestry cases, 165,624 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Glucocorticoid use measurement http://www.ebi.ac.uk/efo/EFO_0009942 GCST90018780 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antihistamines for systemic use) 10,163 East Asian ancestry cases, 168,563 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Antihistamine use measurement http://www.ebi.ac.uk/efo/EFO_0009943 GCST90018781 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antiglaucoma preparations and miotics) 5,911 East Asian ancestry cases, 172,815 East Asian ancestry controls NA Illumina [13429980] (imputed) 3 Antiglaucoma preparations and miotics use measurement http://www.ebi.ac.uk/efo/EFO_0009944 GCST90018782 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Aortic aneurysm 3,230 European ancestry cases, 475,964 European ancestry controls, 1,155 East Asian ancestry cases, 173,601 East Asian ancestry controls NA Affymetrix, Illumina [25843950] (imputed) 7 aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0001666 GCST90018783 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Atopic dermatitis 6,224 European ancestry cases, 475,075 European ancestry controls, 4,296 East Asian ancestry cases, 163,807 East Asian ancestry controls NA Affymetrix, Illumina [25843389] (imputed) 23 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90018784 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Autoimmune hepatitis 821 European ancestry cases, 484,413 European ancestry controls, 85 East Asian ancestry cases, 166,529 East Asian ancestry controls NA Affymetrix, Illumina [25843756] (imputed) 1 Autoimmune Hepatitis http://www.ebi.ac.uk/efo/EFO_0005676 GCST90018785 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Abortion 7,069 European ancestry cases, 250,492 European ancestry controls, 136 East Asian ancestry cases, 82,625 East Asian ancestry controls NA Affymetrix, Illumina [25789421] (imputed) 0 abortion http://www.ebi.ac.uk/efo/EFO_1001491 GCST90018786 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Achilles tendon injury 7,746 European ancestry cases, 349,912 European ancestry controls, 312 East Asian ancestry cases, 175,979 East Asian ancestry controls NA Affymetrix, Illumina [20458085] (imputed) 0 Tendinopathy http://www.ebi.ac.uk/efo/EFO_1001434 GCST90018787 Genome-wide genotyping array 2022-10-19 36143338 Upadhyai P 2022-08-24 Life (Basel) www.ncbi.nlm.nih.gov/pubmed/36143338 Exome-Wide Association Study Reveals Host Genetic Variants Likely Associated with the Severity of COVID-19 in Patients of European Ancestry. COVID-19 (hospitalized vs not hospitalized) 2,199 European ancestry cases, 493 European ancestry controls NA NR [1432135] 3 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90179107 Exome-wide sequencing 2022-10-19 36143338 Upadhyai P 2022-08-24 Life (Basel) www.ncbi.nlm.nih.gov/pubmed/36143338 Exome-Wide Association Study Reveals Host Genetic Variants Likely Associated with the Severity of COVID-19 in Patients of European Ancestry. COVID-19 (covid respiratory support vs without respiratory support) 1,877 European ancestry cases, 815 European ancestry controls NA NR [1432135] 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90179108 Exome-wide sequencing 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1001; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016514 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1002; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016515 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1003; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016516 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1004; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016517 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1005; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016518 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1006; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016519 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1007; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016520 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1008; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016521 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1009; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016522 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1010; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016523 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1011; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016524 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1012; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016525 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1013; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016526 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1014; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016527 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1015; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016528 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1016; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016529 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1017; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016530 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1018; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016531 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1019; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016532 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1020; Facial segment 61; 3D morphology of the under eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016533 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1021; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016534 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1022; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016535 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1023; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016536 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1024; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016537 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1025; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016538 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1026; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016539 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1027; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016540 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1028; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016541 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1029; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016542 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1030; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016543 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1031; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016544 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1032; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016545 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1033; Facial segment 62; 3D morphology of the temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016546 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1034; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016547 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1035; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016548 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1036; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016549 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1037; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016550 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1038; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016551 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1039; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016552 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1040; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016553 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1041; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016554 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1042; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016555 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1043; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016556 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1044; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016557 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1045; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016558 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1046; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016559 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1047; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016560 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1048; Facial segment 63; 3D morphology of the cheekbones 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 cheekbone morphology measurement http://www.ebi.ac.uk/efo/EFO_0007847 GCST90016561 Genome-wide genotyping array 2023-11-14 37731612 Breno M 2023-08-16 iScience www.ncbi.nlm.nih.gov/pubmed/37731612 A GWAS in the pandemic epicenter highlights the severe COVID-19 risk locus introgressed by Neanderthals. Severe COVID-19 infection 397 European or unknown ancestry cases, 798 European or unknown ancestry controls NA NR [8910189] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90297537 Genome-wide genotyping array 2023-11-14 37731612 Breno M 2023-08-16 iScience www.ncbi.nlm.nih.gov/pubmed/37731612 A GWAS in the pandemic epicenter highlights the severe COVID-19 risk locus introgressed by Neanderthals. COVID-19 susceptibility 796 European or unknown ancestry cases, 399 European or unknown ancestry controls NA NR [8910189] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90297538 Genome-wide genotyping array 2022-10-18 34565479 Yang S 2021-09-26 Cancer Metab www.ncbi.nlm.nih.gov/pubmed/34565479 mGWAS identification of six novel single nucleotide polymorphism loci with strong correlation to gastric cancer. Dihydrobiopterin levels 466 East Asian ancestry individuals NA NR [258544] 1 dihydrobiopterin measurement http://www.ebi.ac.uk/efo/EFO_0801076 GCST90054804 Genome-wide genotyping array 2022-10-18 34565479 Yang S 2021-09-26 Cancer Metab www.ncbi.nlm.nih.gov/pubmed/34565479 mGWAS identification of six novel single nucleotide polymorphism loci with strong correlation to gastric cancer. Platelet-activating factor levels 466 East Asian ancestry individuals NA NR [258544] 4 platelet-activating factor measurement http://www.ebi.ac.uk/efo/EFO_0801075 GCST90054805 Genome-wide genotyping array 2022-10-18 34565479 Yang S 2021-09-26 Cancer Metab www.ncbi.nlm.nih.gov/pubmed/34565479 mGWAS identification of six novel single nucleotide polymorphism loci with strong correlation to gastric cancer. Ceramide (d18:0/12:0) levels 466 East Asian ancestry individuals NA NR [258544] 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90054806 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (18:0_20:3) levels 6,784 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylinositol (18:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045157 GCST90277363 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (18:0_20:4) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 7 level of Phosphatidylinositol (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045158 GCST90277364 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (18:1_18:1) levels 7,164 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylinositol (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045159 GCST90277365 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (18:1_18:2) levels 6,489 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylinositol (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045160 GCST90277366 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylinositol (18:1_20:4) levels 5,882 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylinositol (18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045161 GCST90277367 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d32:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Sphingomyelin (d32:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045173 GCST90277368 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d34:0) levels 6,207 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Sphingomyelin (d34:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045176 GCST90277369 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d34:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Sphingomyelin (d34:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045175 GCST90277370 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d34:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Sphingomyelin (d34:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045174 GCST90277371 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d36:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Sphingomyelin (d36:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045178 GCST90277372 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d36:2) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Sphingomyelin (d36:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045177 GCST90277373 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d38:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Sphingomyelin (d38:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045180 GCST90277374 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d38:2) levels 7,150 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Sphingomyelin (d38:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045179 GCST90277375 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d40:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Sphingomyelin (d40:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045182 GCST90277376 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d40:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Sphingomyelin (d40:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045181 GCST90277377 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Sphingomyelin (d42:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Sphingomyelin (d42:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045183 GCST90277378 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (46:1) levels 6,070 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 triacylglycerol 46:1 measurement http://www.ebi.ac.uk/efo/EFO_0010401 GCST90277379 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (46:2) levels 5,448 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 triacylglycerol 46:2 measurement http://www.ebi.ac.uk/efo/EFO_0010402 GCST90277380 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (48:0) levels 5,463 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90277381 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (48:1) levels 7,019 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90277382 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (48:2) levels 7,071 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90277383 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (48:3) levels 6,855 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90277384 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (49:1) levels 5,843 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90277385 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (49:2) levels 6,076 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Triacylglycerol (49:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045162 GCST90277386 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (50:1) levels 7,143 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90277387 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (50:2) levels 7,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90277388 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (50:3) levels 7,161 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90277389 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (50:4) levels 7,166 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90277390 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (50:5) levels 5,491 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 triacylglycerol 50:5 measurement http://www.ebi.ac.uk/efo/EFO_0010412 GCST90277391 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (51:1) levels 5,495 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90277392 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (51:2) levels 7,149 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90277393 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (51:3) levels 7,119 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Triacylglycerol (51:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045163 GCST90277394 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (51:4) levels 5,237 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Triacylglycerol (51:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045164 GCST90277395 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (52:2) levels 7,168 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90277396 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (52:3) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90277397 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (52:4) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 7 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90277398 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (52:5) levels 7,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 52:5 measurement http://www.ebi.ac.uk/efo/EFO_0010417 GCST90277399 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (52:6) levels 6,554 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 52:6 measurement http://www.ebi.ac.uk/efo/EFO_0010418 GCST90277400 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (53:2) levels 6,996 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90277401 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (53:3) levels 7,113 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Triacylglycerol (53:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045165 GCST90277402 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (53:4) levels 6,479 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Triacylglycerol (53:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045166 GCST90277403 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (54:3) levels 7,162 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90277404 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (54:4) levels 7,165 Finnish ancestry individuals NA Illumina [11318730] (imputed) 7 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90277405 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (54:5) levels 7,146 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90277406 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (54:6) levels 7,066 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90277407 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (54:7) levels 6,828 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 54:7 measurement http://www.ebi.ac.uk/efo/EFO_0010425 GCST90277408 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (56:3) levels 6,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 56:3 measurement http://www.ebi.ac.uk/efo/EFO_0010430 GCST90277409 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (56:4) levels 5,820 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 triacylglycerol 56:4 measurement http://www.ebi.ac.uk/efo/EFO_0010431 GCST90277410 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (56:5) levels 5,490 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 triacylglycerol 56:5 measurement http://www.ebi.ac.uk/efo/EFO_0010432 GCST90277411 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (56:6) levels 7,151 Finnish ancestry individuals NA Illumina [11318730] (imputed) 7 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90277412 Genome-wide genotyping array 2022-09-14 35902621 Bae JS 2022-07-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35902621 Clinical significance of germline telomere length and associated genetic factors in patients with neuroblastoma. Germline telomere length in neuroblastoma 186 individuals NA Illumina [248399] 11 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90134644 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (56:7) levels 7,148 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 triacylglycerol 56:7 measurement http://www.ebi.ac.uk/efo/EFO_0010434 GCST90277413 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (56:8) levels 6,800 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90277414 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (58:7) levels 5,403 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 triacylglycerol 58:7 measurement http://www.ebi.ac.uk/efo/EFO_0010441 GCST90277415 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Triacylglycerol (58:8) levels 6,384 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90277416 Genome-wide genotyping array 2022-09-21 35927536 Fan J 2022-08-04 Eur J Clin Microbiol Infect Dis www.ncbi.nlm.nih.gov/pubmed/35927536 Genome-wide association study of SARS-CoV-2 infection in Chinese population. COVID-19 87 Han Chinese ancestry symptomatic cases, 85 Han Chinese ancestry close contact controls NA Illumina [194883] 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90137496 Exome-wide sequencing 2022-09-21 35927536 Fan J 2022-08-04 Eur J Clin Microbiol Infect Dis www.ncbi.nlm.nih.gov/pubmed/35927536 Genome-wide association study of SARS-CoV-2 infection in Chinese population. COVID-19 severity 87 Han Chinese ancestry symptomatic cases, 84 Han Chinese ancestry asymptomatic cases NA Illumina [194805] 0 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90137497 Exome-wide sequencing 2022-09-21 35927536 Fan J 2022-08-04 Eur J Clin Microbiol Infect Dis www.ncbi.nlm.nih.gov/pubmed/35927536 Genome-wide association study of SARS-CoV-2 infection in Chinese population. Asymptomatic COVID-19 infection 84 Han Chinese ancestry asymptomatic cases, 85 Han Chinese ancestry close contact controls NA Illumina [194805] 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90137498 Exome-wide sequencing 2022-04-08 34861174 Shaw DM 2021-12-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34861174 Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. Predicted developmental stuttering 6,339 European ancestry cases, 33,172 European ancestry controls NA Illumina [7751954] (imputed) 12 Stuttering http://purl.obolibrary.org/obo/HP_0025268 GCST90100563 Genome-wide genotyping array 2022-04-08 34861174 Shaw DM 2021-12-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34861174 Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. Predicted developmental stuttering 1,853 African ancestry cases, 8,372 African ancestry controls NA Illumina [13643593] (imputed) 53 Stuttering http://purl.obolibrary.org/obo/HP_0025268 GCST90100564 Genome-wide genotyping array 2022-04-08 34861174 Shaw DM 2021-12-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34861174 Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. Predicted developmental stuttering 124 East Asian ancestry cases, 592 East Asian ancestry controls NA Illumina [6922517] (imputed) 7 Stuttering http://purl.obolibrary.org/obo/HP_0025268 GCST90100565 Genome-wide genotyping array 2022-04-08 34861174 Shaw DM 2021-12-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34861174 Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. Predicted developmental stuttering 51 South Asian ancestry cases, 228 South Asian ancestry controls NA Illumina [7058354] (imputed) 1 Stuttering http://purl.obolibrary.org/obo/HP_0025268 GCST90100566 Genome-wide genotyping array 2022-04-08 34861174 Shaw DM 2021-12-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34861174 Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. Predicted developmental stuttering 397 Hispanic cases, 1,395 Hispanic controls NA Illumina [8147169] (imputed) 13 Stuttering http://purl.obolibrary.org/obo/HP_0025268 GCST90100567 Genome-wide genotyping array 2022-04-08 34861174 Shaw DM 2021-12-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34861174 Phenome risk classification enables phenotypic imputation and gene discovery in developmental stuttering. Developmental stuttering 1,132 European ancestry cases, 6,111 European ancestry controls, 68 African ancestry cases, 400 African ancestry controls, 42 East Asian ancestry cases, 116 East Asian ancestry controls, 44 South Asian ancestry cases, 148 South Asian ancestry controls, 38 Hispanic cases, 132 Hispanic controls, 21 Mixed or unknown ancestry cases, 112 Mixed or unknown ancestry controls NA NR [7570420] (imputed) 0 Stuttering http://purl.obolibrary.org/obo/HP_0025268 GCST90101764 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1297|superpathway of purine deoxyribonucleosides degradation) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026943 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1298|superpathway of pyrimidine deoxyribonucleosides degradation) 315 Chinese ancestry individuals NA Illumina [492582] 22 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026944 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1319|CDP-diacylglycerol biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026945 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1415|superpathway of heme biosynthesis from uroporphyrinogen-III) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026946 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1479|tRNA processing) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026947 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1533|methylphosphonate degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 22 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026948 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1586|peptidoglycan maturation (meso-diaminopimelate containing)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026949 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-162|superpathway of pyrimidine ribonucleotides de novo biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026950 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-166|superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis (E. coli)) 315 Chinese ancestry individuals NA Illumina [492582] 19 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026951 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-321|phenylacetate degradation I (aerobic)) 315 Chinese ancestry individuals NA Illumina [492582] 36 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026952 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-42|2-methylcitrate cycle I) 315 Chinese ancestry individuals NA Illumina [492582] 22 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026953 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-781|aspartate superpathway) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026954 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-845|superpathway of pyridoxal 5'-phosphate biosynthesis and salvage) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026955 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-862|(5Z)-dodec-5-enoate biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026956 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY1G-0|mycothiol biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 26 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026957 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY490-3|nitrate reduction VI (assimilatory)) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026958 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY4FS-7|phosphatidylglycerol biosynthesis I (plastidic)) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026959 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY4FS-8|phosphatidylglycerol biosynthesis II (non-plastidic)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026960 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWYG-321|mycolate biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026961 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PYRIDNUCSAL-PWY|NAD salvage pathway I) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026962 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PYRIDNUCSYN-PWY|NAD biosynthesis I (from aspartate)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026963 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PYRIDOXSYN-PWY|pyridoxal 5'-phosphate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026964 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (REDCITCYC|TCA cycle VIII (helicobacter)) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026965 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (RHAMCAT-PWY|L-rhamnose degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026966 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (RIBOSYN2-PWY|flavin biosynthesis I (bacteria and plants)) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026967 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7237|myo-, chiro- and scillo-inositol degradation) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026918 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7242|D-fructuronate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026919 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7254|TCA cycle VII (acetate-producers)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026920 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7315|dTDP-N-acetylthomosamine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 16 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026921 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7323|superpathway of GDP-mannose-derived O-antigen building blocks biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026922 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7328|superpathway of UDP-glucose-derived O-antigen building blocks biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026923 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7332|superpathway of UDP-N-acetylglucosamine-derived O-antigen building blocks biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 14 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026924 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7371|1,4-dihydroxy-6-naphthoate biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 22 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026925 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7373|superpathway of demethylmenaquinol-6 biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 27 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026926 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7376|cob(II)yrinate a,c-diamide biosynthesis II (late cobalt incorporation)) 315 Chinese ancestry individuals NA Illumina [492582] 17 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026927 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7377|cob(II)yrinate a,c-diamide biosynthesis I (early cobalt insertion)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026928 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7392|taxadiene biosynthesis (engineered)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026929 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7400|L-arginine biosynthesis IV (archaebacteria)) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026930 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7431|aromatic biogenic amine degradation (bacteria)) 315 Chinese ancestry individuals NA Illumina [492582] 11 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026931 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7456|mannan degradation) 315 Chinese ancestry individuals NA Illumina [492582] 15 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026932 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7539|6-hydroxymethyl-dihydropterin diphosphate biosynthesis III (Chlamydia)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026933 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7560|methylerythritol phosphate pathway II) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026934 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7663|gondoate biosynthesis (anaerobic)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026935 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7664|oleate biosynthesis IV (anaerobic)) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026936 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-841|superpathway of purine nucleotides de novo biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026937 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-922|mevalonate pathway I) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026938 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1061|superpathway of L-alanine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026939 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1241|ADP-L-glycero-β-D-manno-heptose biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026940 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1261|anhydromuropeptides recycling) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026941 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY0-1296|purine ribonucleosides degradation) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026942 Genome-wide genotyping array 2022-08-19 35551307 Mahajan A 2022-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35551307 Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Type 2 diabetes 251,740 European ancestry individuals, 139,705 East Asian ancestry individuals, 40,737 South Asian ancestry individuals, 27,417 Hispanic individuals, 30,167 African American individuals, 2,426 Zulu ancestry individuals NA Affymetrix, Illumina [10454876] (imputed) 338 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90132183 Genome-wide genotyping array, Exome-wide sequencing 2022-08-19 35551307 Mahajan A 2022-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35551307 Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Type 2 diabetes 251,740 European ancestry individuals NA Affymetrix, Illumina [10454876] (imputed) 283 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90132184 Genome-wide genotyping array 2022-08-19 35551307 Mahajan A 2022-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35551307 Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Type 2 diabetes 139,705 East Asian ancestry individuals NA Affymetrix, Illumina [9106251] (imputed) 143 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90132185 Genome-wide genotyping array 2022-08-19 35551307 Mahajan A 2022-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35551307 Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Type 2 diabetes 40,737 South Asian ancestry individuals NA Affymetrix, Illumina [10401622] (imputed) 26 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90132186 Genome-wide genotyping array 2022-08-19 35551307 Mahajan A 2022-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35551307 Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Type 2 diabetes 27,417 Hispanic individuals NA Affymetrix, Illumina [NR] (imputed) 31 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90132187 Genome-wide genotyping array, Exome-wide sequencing 2022-08-19 35551307 Mahajan A 2022-05-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35551307 Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Type 2 diabetes 30,167 African American individuals, 2,426 Zulu ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 6 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90132188 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (f_Aerococcaceae) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026991 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (f_Bifidobacteriaceae) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026992 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (f_Lachnospiraceae) 315 Chinese ancestry individuals NA Illumina [492582] 14 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026993 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (f_Mycoplasmataceae) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026994 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (f_Peptostreptococcales-Tissierellales) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026995 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (f_Veillonellaceae) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026996 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Anaerococcus) 315 Chinese ancestry individuals NA Illumina [492582] 17 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026997 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Atopobium) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026998 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Dialister) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026999 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Lactobacillus) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027000 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Megasphaera) 315 Chinese ancestry individuals NA Illumina [492582] 11 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027001 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Peptoniphilus) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027002 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Prevotella) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027003 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (g_Streptococcus) 315 Chinese ancestry individuals NA Illumina [492582] 21 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027004 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (o_Bacteroidales) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026988 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (o_Campylobacterales) 315 Chinese ancestry individuals NA Illumina [492582] 21 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026989 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (o_Fusobacteriales) 315 Chinese ancestry individuals NA Illumina [492582] 28 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026666 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (o_Peptostreptococcales-Tissierellales) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026990 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (p_Actinobacteriota) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026983 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (p_Firmicutes) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026984 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (p_Proteobacteria) 315 Chinese ancestry individuals NA Illumina [492582] 17 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026985 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Aerococcus christensenii) 315 Chinese ancestry individuals NA Illumina [492582] 29 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027005 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Atopobium vaginae) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027006 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Dialister micraerophilus) 315 Chinese ancestry individuals NA Illumina [492582] 19 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027007 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Dialister propionicifaciens) 315 Chinese ancestry individuals NA Illumina [492582] 44 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027008 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Peptoniphilus vaginalis) 315 Chinese ancestry individuals NA Illumina [492582] 30 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027018 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Prevotella bivia) 315 Chinese ancestry individuals NA Illumina [492582] 13 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027019 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Prevotella timonensis) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027020 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (Lactobacillus crispatus or Lactobacillus iners or Gardnerella vaginalis) (pleiotropy) 315 Chinese ancestry individuals NA Illumina [492582] 20 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90132230 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (pleiotropy) 315 Chinese ancestry individuals NA Illumina [492582] 14 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90132231 Genome-wide genotyping array 2023-06-21 36737517 Akiyama M 2023-02-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36737517 Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals. Lifespan 78,029 Japanese ancestry males NA Illumina [6108833] (imputed) 1 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST90270907 Genome-wide genotyping array 2023-06-21 36737517 Akiyama M 2023-02-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36737517 Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals. Lifespan 59,664 Japanese ancestry females NA Illumina [6108833] (imputed) 0 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST90270908 Genome-wide genotyping array 2023-06-21 36737517 Akiyama M 2023-02-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36737517 Genome-wide association study reveals BET1L associated with survival time in the 137,693 Japanese individuals. Lifespan 137,693 Japanese ancestry individuals NA Illumina [6108833] (imputed) 1 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST90270909 Genome-wide genotyping array 2022-04-28 35132194 Nakamura Y 2022-02-07 Eur J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/35132194 A genome-wide association study on adherence to low-carbohydrate diets in Japanese. Low-carbohydrate diet (LCD) score 14,076 East Asian ancestry individuals NA Illumina [7067967] (imputed) 17 carbohydrate intake measurement http://www.ebi.ac.uk/efo/EFO_0010811 GCST90102254 Genome-wide genotyping array 2022-04-28 35132194 Nakamura Y 2022-02-07 Eur J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/35132194 A genome-wide association study on adherence to low-carbohydrate diets in Japanese. Low-carbohydrate diet (LCD) score 6,332 East Asian ancestry male individuals NA Illumina [7067967] (imputed) 12 carbohydrate intake measurement http://www.ebi.ac.uk/efo/EFO_0010811 GCST90102255 Genome-wide genotyping array 2022-06-08 35542997 Schneider LS 2022-01-01 J Prev Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35542997 A Polymorphism Cluster at the 2q12 locus May Predict Response to Piromelatine in Patients with Mild Alzheimer's Disease. Response to piromelatine in mild Alzheimer's disease 107 individuals NA NR [NR] 0 response to piromelatine http://www.ebi.ac.uk/efo/EFO_0021422 GCST90103800 Genome-wide sequencing, Exome-wide sequencing 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5659|GDP-mannose biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026818 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5667|CDP-diacylglycerol biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026819 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5676|acetyl-CoA fermentation to butanoate II) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026820 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5677|succinate fermentation to butanoate) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026821 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5686|UMP biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026822 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5695|urate biosynthesis/inosine 5'-phosphate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 26 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026823 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5705|allantoin degradation to glyoxylate III) 315 Chinese ancestry individuals NA Illumina [492582] 33 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026824 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5741|ethylmalonyl-CoA pathway) 315 Chinese ancestry individuals NA Illumina [492582] 49 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026825 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5747|2-methylcitrate cycle II) 315 Chinese ancestry individuals NA Illumina [492582] 35 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026826 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5837|1,4-dihydroxy-2-naphthoate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026827 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5838|superpathway of menaquinol-8 biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026828 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5840|superpathway of menaquinol-7 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026829 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5845|superpathway of menaquinol-9 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 25 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026830 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5850|superpathway of menaquinol-6 biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 25 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026831 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5855|ubiquinol-7 biosynthesis (prokaryotic)) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026832 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5856|ubiquinol-9 biosynthesis (prokaryotic)) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026833 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5857|ubiquinol-10 biosynthesis (prokaryotic)) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026834 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5860|superpathway of demethylmenaquinol-6 biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 20 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026835 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5861|superpathway of demethylmenaquinol-8 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 13 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026836 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5862|superpathway of demethylmenaquinol-9 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 27 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026837 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5863|superpathway of phylloquinol biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 23 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026838 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5896|superpathway of menaquinol-10 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 27 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026839 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5897|superpathway of menaquinol-11 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026840 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5898|superpathway of menaquinol-12 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026841 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5899|superpathway of menaquinol-13 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026842 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5910|superpathway of geranylgeranyldiphosphate biosynthesis I (via mevalonate)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026843 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5913|TCA cycle VI (obligate autotrophs)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026844 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5918|superpathay of heme biosynthesis from glutamate) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026845 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5920|superpathway of heme biosynthesis from glycine) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026846 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5971|palmitate biosynthesis II (bacteria and plants)) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026847 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5973|cis-vaccenate biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026848 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5989|stearate biosynthesis II (bacteria and plants)) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026849 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6121|5-aminoimidazole ribonucleotide biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026850 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6122|5-aminoimidazole ribonucleotide biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026851 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6123|inosine-5'-phosphate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026852 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6125|superpathway of guanosine nucleotides de novo biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026853 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6700|queuosine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026886 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6126|superpathway of adenosine nucleotides de novo biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026854 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6147|6-hydroxymethyl-dihydropterin diphosphate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026855 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6151|S-adenosyl-L-methionine cycle I) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026856 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6163|chorismate biosynthesis from 3-dehydroquinate) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026857 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-621|sucrose degradation III (sucrose invertase)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026858 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6263|superpathway of menaquinol-8 biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026859 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6269|adenosylcobalamin salvage from cobinamide II) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026860 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6277|superpathway of 5-aminoimidazole ribonucleotide biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026861 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6282|palmitoleate biosynthesis I (from (5Z)-dodec-5-enoate)) 315 Chinese ancestry individuals NA Illumina [492582] 14 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026862 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6317|galactose degradation I (Leloir pathway)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026863 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6353|purine nucleotides degradation II (aerobic)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026864 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6383|mono-trans, poly-cis decaprenyl phosphate biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026865 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6385|peptidoglycan biosynthesis III (mycobacteria)) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026866 Genome-wide genotyping array 2022-05-24 35228297 Joseph CB 2022-03-01 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/35228297 Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin. Urinary uromodulin levels (raw) 29,315 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 26 urinary uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0005663 GCST90103502 Genome-wide genotyping array 2022-05-24 35228297 Joseph CB 2022-03-01 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/35228297 Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin. Urinary uromodulin levels (indexed to creatinine) 29,315 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 43 urinary uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0005663 GCST90103503 Genome-wide genotyping array 2022-04-27 35168826 Wood AC 2022-01-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35168826 Identification of genetic loci simultaneously associated with multiple cardiometabolic traits. Diastolic blood pressure 453,413 European ancestry individuals NA Affymetrix [NR] (imputed) 4 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90102270 Genome-wide genotyping array 2022-04-27 35168826 Wood AC 2022-01-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35168826 Identification of genetic loci simultaneously associated with multiple cardiometabolic traits. Hemoglobin A1c levels 417,018 European ancestry individuals NA Affymetrix [NR] (imputed) 4 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90102271 Genome-wide genotyping array 2022-04-27 35168826 Wood AC 2022-01-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35168826 Identification of genetic loci simultaneously associated with multiple cardiometabolic traits. Systolic blood pressure 453,413 European ancestry individuals NA Affymetrix [NR] (imputed) 4 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90102269 Genome-wide genotyping array 2022-04-27 35168826 Wood AC 2022-01-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35168826 Identification of genetic loci simultaneously associated with multiple cardiometabolic traits. Low density lipoprotein cholesterol levels 431,167 European ancestry individuals NA Affymetrix [NR] (imputed) 4 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90102272 Genome-wide genotyping array 2022-04-27 35168826 Wood AC 2022-01-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35168826 Identification of genetic loci simultaneously associated with multiple cardiometabolic traits. High density lipoprotein cholesterol levels 397,721 European ancestry individuals NA Affymetrix [NR] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90102273 Genome-wide genotyping array 2022-04-27 35168826 Wood AC 2022-01-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35168826 Identification of genetic loci simultaneously associated with multiple cardiometabolic traits. Waist-to-hip ratio adjusted for BMI 456,823 European ancestry individuals NA Affymetrix [NR] (imputed) 4 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90102274 Genome-wide genotyping array 2022-04-27 35168826 Wood AC 2022-01-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35168826 Identification of genetic loci simultaneously associated with multiple cardiometabolic traits. Triglyceride levels 356,574 European ancestry individuals NA Affymetrix [NR] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102275 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d43:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917403] (imputed) 8 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101942 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d44:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917404] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101943 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cis androsterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917405] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101944 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cortexolone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917406] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101945 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cortexone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917407] (imputed) 1 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101946 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Corticosterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917408] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101947 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cortisol levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917409] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90101948 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cortisol sulfate levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917410] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90101949 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cortisone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917411] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101950 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Diglycerides (32:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917412] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90101951 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Diglycerides (34:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917413] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90101952 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Diglycerides (34:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917414] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90101953 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Diglycerides (36:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917415] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90101954 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Diglycerides (36:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917416] (imputed) 1 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90101955 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Diglycerides (36:4)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917417] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90101956 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Diglycerides (38:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917418] (imputed) 2 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90101957 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Dehydroepiandrosterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917419] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101958 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Dehydroepiandrosterone sulfate levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917420] (imputed) 0 dehydroepiandrosterone measurement http://www.ebi.ac.uk/efo/EFO_0010240 GCST90101959 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Dihydroprogesterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917421] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101960 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Dihydrotestosterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917422] (imputed) 0 dihydrotestosterone measurement http://www.ebi.ac.uk/efo/EFO_0004909 GCST90101961 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Estradiol levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917423] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90101962 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Estriol levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917424] (imputed) 8 estrogen measurement http://www.ebi.ac.uk/efo/EFO_0011007 GCST90101963 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Estrone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917425] (imputed) 0 estrone measurement http://www.ebi.ac.uk/efo/EFO_0007970 GCST90101964 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (10:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917426] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101965 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (11:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917427] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101966 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (RUMP-PWY|formaldehyde oxidation I) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026968 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (SALVADEHYPOX-PWY|adenosine nucleotides degradation II) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026969 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (SER-GLYSYN-PWY|superpathway of L-serine and glycine biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026970 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (SO4ASSIM-PWY|sulfate reduction I (assimilatory)) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026971 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (SULFATE-CYS-PWY|superpathway of sulfate assimilation and cysteine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026972 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (TCA|TCA cycle I (prokaryotic)) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026973 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (TCA-GLYOX-BYPASS|superpathway of glyoxylate bypass and TCA) 315 Chinese ancestry individuals NA Illumina [492582] 13 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026664 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (TEICHOICACID-PWY|teichoic acid (poly-glycerol) biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026974 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (THISYN-PWY|superpathway of thiamin diphosphate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026975 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (THRESYN-PWY|superpathway of L-threonine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026976 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (TRNA-CHARGING-PWY|tRNA charging) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026977 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (TRPSYN-PWY|L-tryptophan biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026978 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (TYRFUMCAT-PWY|L-tyrosine degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 20 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026979 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (UBISYN-PWY|superpathway of ubiquinol-8 biosynthesis (prokaryotic)) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026980 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (UDPNAGSYN-PWY|UDP-N-acetyl-D-glucosamine biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026981 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (VALSYN-PWY|L-valine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026982 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (c_Actinobacteria) 315 Chinese ancestry individuals NA Illumina [492582] 13 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026672 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (c_Clostridia) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026673 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (c_Gammaproteobacteria) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026674 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (f_Aerococcaceae) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026678 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (f_Bifidobacteriaceae) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026679 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (f_Lachnospiraceae) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026680 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (f_Mycoplasmataceae) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026681 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (f_Peptostreptococcales-Tissierellales) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026682 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (f_Veillonellaceae) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026683 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Glycosphingolipids (d42:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917357] (imputed) 37 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90094887 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (36:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917357] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90094888 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d34:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917357] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90094886 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d32:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917357] (imputed) 26 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90094889 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d40:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917357] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90094890 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. 17-hydroxyprogesterone (17-OHP) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917358] (imputed) 0 17-hydroxyprogesterone measurement http://www.ebi.ac.uk/efo/EFO_0010220 GCST90101897 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. 17 hydroxypregnenolone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917359] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101898 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. 2 methoxyestradiol levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917360] (imputed) 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90101899 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. 20 hydroxyprogesterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917361] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101900 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (10:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917362] (imputed) 1 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101901 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (10:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917363] (imputed) 1 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101902 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (12:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917364] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101903 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (12:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917365] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101904 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (14:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917366] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101905 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (14:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917367] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101906 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (16:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917368] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101907 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (18:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917369] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101908 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (18:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917370] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101909 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Acylcarnitine (18:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917371] (imputed) 0 acylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0005059 GCST90101910 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Aldosterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917372] (imputed) 1 aldosterone measurement http://www.ebi.ac.uk/efo/EFO_0010219 GCST90101911 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Allo pregnolone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917373] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101912 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Androstanediol levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917374] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101913 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Androstenediol levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917375] (imputed) 3 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101914 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Androstenedione levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917376] (imputed) 0 androstenedione measurement http://www.ebi.ac.uk/efo/EFO_0007972 GCST90101915 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Beta pregnolone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917377] (imputed) 1 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90101916 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (16:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917378] (imputed) 0 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90101917 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (16:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917379] (imputed) 0 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90101918 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (18:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917380] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90101919 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (18:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917381] (imputed) 2 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90101920 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (18:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917382] (imputed) 1 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90101921 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (20:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917383] (imputed) 1 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90101922 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (20:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917384] (imputed) 3 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90101923 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (20:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917385] (imputed) 2 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90101924 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Cholesteryl ester (22:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917386] (imputed) 0 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90101925 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d32:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917387] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101926 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d33:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917388] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101927 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d34:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917389] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101928 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d34:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917390] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101929 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d34:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917391] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101930 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d36:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917392] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101931 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d38:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917393] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101932 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d39:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917394] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101933 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d40:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917395] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101934 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d40:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917396] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101935 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d40:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917397] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101936 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d41:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917398] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101937 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d42:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917399] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101938 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d42:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917400] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101939 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d42:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917401] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101940 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Ceramide (d42:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917402] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90101941 Genome-wide genotyping array 2022-06-14 35330412 Grant CW 2022-03-06 J Pers Med www.ncbi.nlm.nih.gov/pubmed/35330412 Multi-Omics Characterization of Early- and Adult-Onset Major Depressive Disorder. Depression (age of onset) 486 European ancestry individuals NA Illumina [7017931] (imputed) 11 unipolar depression, age at onset http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90104443 Genome-wide genotyping array 2022-06-14 35330412 Grant CW 2022-03-06 J Pers Med www.ncbi.nlm.nih.gov/pubmed/35330412 Multi-Omics Characterization of Early- and Adult-Onset Major Depressive Disorder. Depression (age of onset) 295 European ancestry individuals NA Illumina [8286413] (imputed) 18 unipolar depression, age at onset http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90104444 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (12:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917428] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101967 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (13:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917429] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101968 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (14:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917430] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101969 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (14:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917431] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101970 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (15:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917432] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101971 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (15:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917433] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101972 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (16:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917434] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101973 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (17:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917435] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101974 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (18:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917436] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101975 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (18:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917437] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101976 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (18:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917438] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101977 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (20:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917439] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101978 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (20:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917440] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101979 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (20:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917441] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101980 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (20:3)W3 levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917442] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101981 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (20:3)W6 levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917443] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101982 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (20:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917444] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101983 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (20:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917445] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101984 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (22:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917446] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101985 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (22:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917447] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101986 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (22:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917448] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101987 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (24:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917449] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101988 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (24:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917450] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101989 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (26:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917451] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101990 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (28:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917452] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101991 Genome-wide genotyping array 2023-05-16 36707530 Kim J 2023-01-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36707530 Investigation of genetic variants and causal biomarkers associated with brain aging. Lower thalamus volume 34,129 British ancestry individuals NA NR [38000000] (imputed) 6 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST90269831 Genome-wide genotyping array 2023-05-16 36707530 Kim J 2023-01-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36707530 Investigation of genetic variants and causal biomarkers associated with brain aging. Fornix volume 34,129 British ancestry individuals NA NR [38000000] (imputed) 6 fornix volume measurement http://www.ebi.ac.uk/efo/EFO_0803381 GCST90269832 Genome-wide genotyping array 2023-05-16 36707530 Kim J 2023-01-27 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36707530 Investigation of genetic variants and causal biomarkers associated with brain aging. Brain age (difference between predicted and chronological age) 34,129 British ancestry individuals NA NR [38000000] (imputed) 6 brain age measurement http://www.ebi.ac.uk/efo/EFO_0010602 GCST90269833 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer adjusted for industrial classification factors 350 Japanese ancestry cases, 434 Japanese ancestry controls NA Illumina [11175945] (imputed) 0 urinary bladder cancer, employment status http://purl.obolibrary.org/obo/MONDO_0001187, http://www.ebi.ac.uk/efo/EFO_0005241 GCST90104599 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer in selected industrial classification factors (Information and communications, Scientific research, professional and technical services, Government, except elsewhere classified) 350 Japanese ancestry cases, 434 Japanese ancestry controls NA Illumina [11175945] (imputed) 0 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90104600 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer adjusted for occupational classification factors 350 Japanese ancestry cases, 434 Japanese ancestry controls NA Illumina [11175945] (imputed) 0 urinary bladder cancer, employment status http://purl.obolibrary.org/obo/MONDO_0001187, http://www.ebi.ac.uk/efo/EFO_0005241 GCST90104601 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer in selected occupational classification factor (security workers) 350 Japanese ancestry cases, 434 Japanese ancestry controls NA Illumina [11175945] (imputed) 0 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90104602 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer in selected industrial classification factors within Construction, Manufacturing, and Transport and Postal Services 350 Japanese ancestry cases, 434 Japanese ancestry controls NA Illumina [11175945] (imputed) 0 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90104603 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer adjusted for occupation (Zaitsu classification) 350 Japanese ancestry cases, 434 Japanese ancestry controls NA Illumina [11175945] (imputed) 0 urinary bladder cancer, employment status http://purl.obolibrary.org/obo/MONDO_0001187, http://www.ebi.ac.uk/efo/EFO_0005241 GCST90104604 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer adjusted for industrial classification factors 300 Japanese ancestry male cases, 395 Japanese ancestry male controls NA Illumina [11175945] (imputed) 1 urinary bladder cancer, employment status http://purl.obolibrary.org/obo/MONDO_0001187, http://www.ebi.ac.uk/efo/EFO_0005241 GCST90104605 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer in selected industrial classification factors (Information and communications, Scientific research, professional and technical services, Government, except elsewhere classified) 300 Japanese ancestry male cases, 395 Japanese ancestry male controls NA Illumina [11175945] (imputed) 1 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90104606 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer adjusted for occupational classification factors 300 Japanese ancestry male cases, 395 Japanese ancestry male controls NA Illumina [11175945] (imputed) 1 urinary bladder cancer, employment status http://purl.obolibrary.org/obo/MONDO_0001187, http://www.ebi.ac.uk/efo/EFO_0005241 GCST90104607 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer in selected occupational classification factor (security workers) 300 Japanese ancestry male cases, 395 Japanese ancestry male controls NA Illumina [11175945] (imputed) 1 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90104608 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer in selected industrial classification factors within Construction, Manufacturing, and Transport and Postal Services 300 Japanese ancestry male cases, 395 Japanese ancestry male controls NA Illumina [11175945] (imputed) 1 urinary bladder cancer http://purl.obolibrary.org/obo/MONDO_0001187 GCST90104609 Genome-wide genotyping array 2022-06-17 35328002 Takeuchi T 2022-02-28 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35328002 Genome-Wide Association Study Adjusted for Occupational and Environmental Factors for Bladder Cancer Susceptibility. Bladder cancer adjusted for occupation (Zaitsu classification) 300 Japanese ancestry male cases, 395 Japanese ancestry male controls NA Illumina [11175945] (imputed) 0 urinary bladder cancer, employment status http://purl.obolibrary.org/obo/MONDO_0001187, http://www.ebi.ac.uk/efo/EFO_0005241 GCST90104610 Genome-wide genotyping array 2022-06-08 35202912 Wei Y 2022-02-21 Biomed Pharmacother www.ncbi.nlm.nih.gov/pubmed/35202912 Whole-exome sequencing reveals genetic variations in humans with differential sensitivity to sevoflurane：A prospective observational study. End-tidal sevoflurane concentration 500 East Asian ancestry individuals NA Illumina [NR] 0 response to sevoflurane http://www.ebi.ac.uk/efo/EFO_0021424 GCST90103981 Exome-wide sequencing 2022-06-14 35022715 Guggenheim JA 2022-01-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35022715 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia. Refractive error 51,624 European ancestry individuals NA NR [524442] 19 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST90104407 Exome-wide sequencing 2022-06-14 35264422 Ament Z 2022-03-09 Neurology www.ncbi.nlm.nih.gov/pubmed/35264422 Nucleosides Associated With Incident Ischemic Stroke in the REGARDS and JHS Cohorts. Pseudouridine levels 2,043 European or African American individuals NA Illumina [NR] (imputed) 2 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90104473 Genome-wide genotyping array 2022-06-14 35264422 Ament Z 2022-03-09 Neurology www.ncbi.nlm.nih.gov/pubmed/35264422 Nucleosides Associated With Incident Ischemic Stroke in the REGARDS and JHS Cohorts. Guanosine levels 2,043 European or African American individuals NA Illumina [NR] (imputed) 0 guanosine measurement http://www.ebi.ac.uk/efo/EFO_0021124 GCST90104474 Genome-wide genotyping array 2022-06-20 35318112 Hajdarevic R 2022-03-19 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/35318112 Genetic association study in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) identifies several potential risk loci. Myalgic encephalomyelitis / chronic fatigue syndrome 427 European ancestry cases, 972 European ancestry controls 2,565 European ancestry cases, 6,751 European ancestry controls Illumina [1462996] (imputed) 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90104622 Genome-wide genotyping array 2022-06-20 35318112 Hajdarevic R 2022-03-19 Brain Behav Immun www.ncbi.nlm.nih.gov/pubmed/35318112 Genetic association study in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) identifies several potential risk loci. Myalgic encephalomyelitis / chronic fatigue syndrome 2,532 European ancestry cases, 5,758 European ancestry controls NA Illumina [NR] (imputed) 5 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90104623 Genome-wide genotyping array 2022-06-14 35031440 Simcoe MJ 2022-01-11 Ophthalmology www.ncbi.nlm.nih.gov/pubmed/35031440 GWAS identifies two common loci associated with pigment dispersion syndrome/pigmentary glaucoma and implicate myopia in its development. Pigment dispersion syndrome or pigmentary glaucoma 179 Pigment dispersion syndrome European ancestry cases, 395 pigmentary glaucoma European ancestry cases, 52,627 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 2 pigment dispersion syndrome, pigmentary glaucoma http://purl.obolibrary.org/obo/MONDO_0010896, http://www.ebi.ac.uk/efo/EFO_0021425 GCST90104349 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Alcohol consumption 141,145 European ancestry individuals 32,779 individuals NR [5745836] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90096892 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Overall healthy diet 258,758 European ancestry individuals up to 32,779 individuals NR [5745834] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096893 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Coffee consumption 105,037 European ancestry individuals up to 32,779 individuals NR [5745847] (imputed) 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90096894 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Fish consumption 308,008 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST90096895 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Fruit consumption 421,155 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096896 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Healthy food consumption 386,047 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096897 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Meat consumption 266,042 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096898 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Psychoactive drinks consumption 127,604 European ancestry individuals up to 32,779 individuals NR [5745834] (imputed) 0 beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010088 GCST90096899 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Vegetables consumption 428,979 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096900 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Beef consumption 241,092 European ancestry individuals 22,697 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096901 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Beer or cider consumption 168,237 European ancestry individuals 24,462 individuals NR [5745855] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90096902 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Spread on bread consumption 445,506 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096903 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Bread consumption 438,853 European ancestry individuals 24,685 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096904 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Champagne or white wine consumption 175,549 European ancestry individuals 16,480 individuals NR [5745855] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90096905 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Cheese consumption 365,842 European ancestry individuals 17,196 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096906 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Cooked vegetables consumption 435,417 European ancestry individuals 33,286 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096907 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Decaffeinated coffee consumption 62,072 European ancestry individuals 6,970 individuals NR [5745849] (imputed) 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90096908 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Dried fruit consumption 409,125 European ancestry individuals 27,137 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096909 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Drink temperature 444,097 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010088 GCST90096910 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Fortified wine consumption 31,836 European ancestry individuals up to 32,779 individuals NR [5747497] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90096911 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Fresh fruit consumption 433,186 European ancestry individuals 35,003 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096912 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Ground coffee consumption 72,276 European ancestry individuals 20,537 individuals NR [5745853] (imputed) 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90096913 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Instant coffee consumption 180,764 European ancestry individuals 20,537 individuals NR [5745855] (imputed) 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90096914 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Lamb consumption 189,984 European ancestry individuals 26,747 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096915 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Percentage fat in milk consumption 411,503 European ancestry individuals 28,740 individuals NR [5745855] (imputed) 0 beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010088 GCST90096916 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Body mass index 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 6 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90140945 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. HDL cholesterol levels 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 29 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90140946 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. LDL cholesterol levels 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 9 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90140947 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Total cholesterol levels 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 25 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90140948 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Triacylglyceride levels 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 23 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90140949 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Systolic blood pressure 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 2 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90140950 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Diastolic blood pressure 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90140951 Genome-wide genotyping array 2022-09-29 35945198 Huang QQ 2022-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35945198 Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals. Coronary artery disease 22,000 Pakistani and Bangladeshi ancestry individuals NA Illumina [9527863] (imputed) 1 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90140952 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Non-oily fish consumption 318,136 European ancestry individuals 35,562 individuals NR [5745855] (imputed) 0 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST90096917 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Oily fish consumption 297,881 European ancestry individuals 39,094 individuals NR [5745855] (imputed) 0 fish consumption measurement http://www.ebi.ac.uk/efo/EFO_0010139 GCST90096918 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Pork consumption 187,202 European ancestry individuals 31,242 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096919 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Poultry consumption 399,716 European ancestry individuals 24,085 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096920 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Processed meat consumption 312,220 European ancestry individuals 31,853 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096921 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Red wine consumption 211,628 European ancestry individuals 16,480 individuals NR [5745855] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90096922 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Salad consumption 422,542 European ancestry individuals 31,310 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096923 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Added salt consumption 323,995 European ancestry individuals 29,397 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096924 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Spirits consumption 118,477 European ancestry individuals 23,009 individuals NR [5745853] (imputed) 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90096925 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Tea consumption 434,171 European ancestry individuals 27,659 individuals NR [5745855] (imputed) 2 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST90096926 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Vegetarianism 442,589 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90096927 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Water consumption corrected for coffee 400,642 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010088 GCST90096928 Genome-wide genotyping array 2022-06-16 35653391 Pirastu N 2022-06-02 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35653391 Using genetic variation to disentangle the complex relationship between food intake and health outcomes. Water consumption 445,799 European ancestry individuals up to 32,779 individuals NR [5745855] (imputed) 0 beverage consumption measurement http://www.ebi.ac.uk/efo/EFO_0010088 GCST90096929 Genome-wide genotyping array 2022-06-23 34427645 Lin WY 2021-08-24 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/34427645 Lifestyle factors and genetic variants on two biological age measures: evidence from 94,443 Taiwan Biobank participants. Biological age (BioAge) 25,460 Taiwanese ancestry individuals 68,983 Taiwanese ancestry individuals Affymetrix [7433014] (imputed) 4 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90104396 Genome-wide genotyping array 2022-06-23 34427645 Lin WY 2021-08-24 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/34427645 Lifestyle factors and genetic variants on two biological age measures: evidence from 94,443 Taiwan Biobank participants. Biological age (PhenoAge) 25,460 Taiwanese ancestry individuals 68,983 Taiwanese ancestry individuals Affymetrix [7433014] (imputed) 11 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90104395 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (HOMOSER-METSYN-PWY|L-methionine biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026748 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (HSERMETANA-PWY|L-methionine biosynthesis III) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026749 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ILEUSYN-PWY|L-isoleucine biosynthesis I (from threonine)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026750 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (KDO-NAGLIPASYN-PWY|superpathway of (Kdo)2-lipid A biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 31 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026751 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (LACTOSECAT-PWY|lactose and galactose degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026752 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (LEU-DEG2-PWY|L-leucine degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 18 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026753 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (MET-SAM-PWY|superpathway of S-adenosyl-L-methionine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026754 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (METH-ACETATE-PWY|methanogenesis from acetate) 315 Chinese ancestry individuals NA Illumina [492582] 51 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026755 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P105-PWY|TCA cycle IV (2-oxoglutarate decarboxylase)) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026663 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (HEXITOLDEGSUPER-PWY|superpathway of hexitol degradation (bacteria)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026745 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (HISDEG-PWY|L-histidine degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026746 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (HISTSYN-PWY|L-histidine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026747 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (NAD-BIOSYNTHESIS-II|NAD salvage pathway II) 315 Chinese ancestry individuals NA Illumina [492582] 31 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026662 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (NAGLIPASYN-PWY|lipid IVA biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026756 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (NONMEVIPP-PWY|methylerythritol phosphate pathway I) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026757 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (NONOXIPENT-PWY|pentose phosphate pathway (non-oxidative branch)) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026758 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (OANTIGEN-PWY|O-antigen building blocks biosynthesis (E. coli)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026759 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P108-PWY|pyruvate fermentation to propanoate I) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026760 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P122-PWY|heterolactic fermentation) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026761 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P124-PWY|Bifidobacterium shunt) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026762 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P125-PWY|superpathway of (R,R)-butanediol biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 27 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026763 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P161-PWY|acetylene degradation) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026764 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P162-PWY|L-glutamate degradation V (via hydroxyglutarate)) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026765 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P163-PWY|L-lysine fermentation to acetate and butanoate) 315 Chinese ancestry individuals NA Illumina [492582] 18 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026766 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P164-PWY|purine nucleobases degradation I (anaerobic)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026767 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (COMPLETE-ARO-PWY|superpathway of aromatic amino acid biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026722 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (DENOVOPURINE2-PWY|superpathway of purine nucleotides de novo biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026723 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (DTDPRHAMSYN-PWY|dTDP-L-rhamnose biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026724 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ENTBACSYN-PWY|enterobactin biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 32 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026725 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (FAO-PWY|fatty acid β-oxidation I) 315 Chinese ancestry individuals NA Illumina [492582] 17 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026726 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (FASYN-ELONG-PWY|fatty acid elongation -- saturated) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026727 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (FASYN-INITIAL-PWY|superpathway of fatty acid biosynthesis initiation (E. coli)) 315 Chinese ancestry individuals NA Illumina [492582] 15 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026728 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (FERMENTATION-PWY|mixed acid fermentation) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026729 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (FOLSYN-PWY|superpathway of tetrahydrofolate biosynthesis and salvage) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026730 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (FUC-RHAMCAT-PWY|superpathway of fucose and rhamnose degradation) 315 Chinese ancestry individuals NA Illumina [492582] 29 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026731 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (FUCCAT-PWY|fucose degradation) 315 Chinese ancestry individuals NA Illumina [492582] 35 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026732 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GALACT-GLUCUROCAT-PWY|superpathway of hexuronide and hexuronate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026733 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GALACTUROCAT-PWY|D-galacturonate degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026734 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLCMANNANAUT-PWY|superpathway of N-acetylglucosamine, N-acetylmannosamine and N-acetylneuraminate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026735 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLUCOSE1PMETAB-PWY|glucose and glucose-1-phosphate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 11 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026736 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLUCUROCAT-PWY|superpathway of β-D-glucuronide and D-glucuronate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026737 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLUTORN-PWY|L-ornithine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026738 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLYCOGENSYNTH-PWY|glycogen biosynthesis I (from ADP-D-Glucose)) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026739 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLYCOLYSIS|glycolysis I (from glucose 6-phosphate)) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026740 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLYCOLYSIS-E-D|superpathway of glycolysis and Entner-Doudoroff) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026741 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLYCOLYSIS-TCA-GLYOX-BYPASS|superpathway of glycolysis, pyruvate dehydrogenase, TCA, and glyoxylate bypass) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026660 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GLYOXYLATE-BYPASS|glyoxylate cycle) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026661 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (GOLPDLCAT-PWY|superpathway of glycerol degradation to 1,3-propanediol) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026742 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (HEME-BIOSYNTHESIS-II|heme biosynthesis I (aerobic)) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026743 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (HEMESYN2-PWY|heme biosynthesis II (anaerobic)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026744 Genome-wide genotyping array 2023-06-14 36603154 Donoghue LJ 2023-01-05 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/36603154 Identification of a Genetic Susceptibility Locus for Idiopathic Pulmonary Fibrosis in the 16p Subtelomere Using Whole Genome Sequencing. Idiopathic pulmonary fibrosis 1,638 cases, 7,947 controls NA NR [5900000] 2 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST90270267 Genome-wide sequencing 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Finegoldia magna) 315 Chinese ancestry individuals NA Illumina [492582] 16 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027009 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Gardnerella vaginalis) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027010 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Lactobacillus crispatus) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027011 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Lactobacillus iners) 315 Chinese ancestry individuals NA Illumina [492582] 11 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027012 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Lactobacillus jensenii) 315 Chinese ancestry individuals NA Illumina [492582] 26 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027013 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Lactobacillus mulieris) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027014 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Lactobacillus paragasseri/gasseri) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027015 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Lactobacillus reuteri) 315 Chinese ancestry individuals NA Illumina [492582] 15 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027016 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (s_Megasphaera genomosp type 1) 315 Chinese ancestry individuals NA Illumina [492582] 22 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90027017 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:8) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917553] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102092 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (42:10) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917554] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102093 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (42:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917555] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102094 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (42:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917556] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102095 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (o-32:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917557] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102096 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (o-34:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917558] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102097 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (34:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917559] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102098 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (34:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917560] (imputed) 5 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102099 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (36:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917561] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102100 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (36:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917562] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102101 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (36:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917563] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102102 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (38:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917564] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102103 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (38:4)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917565] (imputed) 4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102104 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (38:4)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917566] (imputed) 2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102105 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (38:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917567] (imputed) 8 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102106 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylethanolamine (40:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917568] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90102107 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylinositol (36:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917569] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90102108 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylinositol (36:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917570] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90102109 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylinositol (38:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917571] (imputed) 1 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90102110 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylinositol (38:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917572] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90102111 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Pregnenolone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917573] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90102112 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Progesterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917574] (imputed) 0 progesterone measurement http://www.ebi.ac.uk/efo/EFO_0007004 GCST90102113 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d30:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917575] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102114 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d32:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917576] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102115 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d32:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917577] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102116 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d42:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917603] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102142 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d43:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917604] (imputed) 11 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102143 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d43:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917605] (imputed) 14 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102144 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d44:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917606] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102145 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (40:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917607] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102146 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (40:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917608] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102147 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (42:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917609] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102148 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (42:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917610] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102149 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (42:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917611] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102150 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (44:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917612] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102151 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (44:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917613] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102152 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (44:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917614] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102153 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (46:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917615] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102154 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (46:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917616] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102155 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (46:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917617] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102156 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (46:3)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917618] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102157 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (46:3)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917619] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102158 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (46:4)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917620] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102159 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (48:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917621] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102160 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (48:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917622] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102161 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (48:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917623] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102162 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (48:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917624] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102163 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (48:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917625] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102164 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (48:4)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917626] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102165 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (48:4)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917627] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102166 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917678] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102217 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917679] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102218 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917680] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102219 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917681] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102220 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:5)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917682] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102221 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:5)C levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917683] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102222 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:6)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917684] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102223 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:6)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917685] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102224 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:7)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917686] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102225 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:7)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917687] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102226 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:8)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917688] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102227 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:8)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917689] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102228 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:9) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917690] (imputed) 2 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102229 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (57:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917691] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102230 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917692] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102231 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917693] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102232 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:10) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917694] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102233 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917695] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102234 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917696] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102235 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917697] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102236 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917698] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102237 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:8) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917699] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102238 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (58:9) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917700] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102239 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (59:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917701] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102240 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (60:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917702] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102241 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (49:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917628] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102167 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (49:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917629] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102168 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (49:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917630] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102169 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (49:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917631] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102170 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917632] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102171 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917633] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102172 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917634] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102173 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:3)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917635] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102174 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:3)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917636] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102175 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917637] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102176 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:5)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917638] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102177 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (50:5)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917639] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102178 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (51:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917640] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102179 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (51:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917641] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102180 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (51:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917642] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102181 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (51:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917643] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102182 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (51:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917644] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102183 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:0)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917645] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102184 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:0)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917646] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102185 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917647] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102186 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917648] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102187 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917649] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102188 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917650] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102189 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:5)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917651] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102190 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:5)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917652] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102191 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (52:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917653] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102192 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (53:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917654] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102193 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (53:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917655] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102194 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (53:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917656] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102195 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (53:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917657] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102196 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (53:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917658] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102197 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (53:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917659] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102198 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (53:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917660] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102199 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917661] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102200 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917662] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102201 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917663] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102202 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917664] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102203 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917665] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102204 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917666] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102205 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:5)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917667] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102206 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:5)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917668] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102207 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:6)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917669] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102208 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:6)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917670] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102209 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:6)C levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917671] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102210 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:7)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917672] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102211 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (54:7)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917673] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102212 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (55:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917674] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102213 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (55:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917675] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102214 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (55:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917676] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102215 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (56:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917677] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102216 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d33:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917578] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102117 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d34:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917579] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102118 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d34:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917580] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102119 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d36:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917581] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102120 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d36:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917582] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102121 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d36:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917583] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102122 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d36:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917584] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102123 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d37:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917585] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102124 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d38:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917586] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102125 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d38:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917587] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102126 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d38:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917588] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102127 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d39:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917589] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102128 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d39:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917590] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102129 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d40:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917591] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102130 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d40:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917592] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102131 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d40:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917593] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102132 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d40:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917594] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102133 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d41:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917595] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102134 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d41:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917596] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102135 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d41:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917597] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102136 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d42:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917598] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102137 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d42:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917599] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102138 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d42:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917600] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102139 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d42:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917601] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102140 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Sphingomyelin (d42:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917602] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90102141 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (60:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917703] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102242 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Triglycerides (60:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917704] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90102243 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Testosterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917705] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90102244 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Testosterone glucuronide levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917706] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90102245 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Trans androsterone levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917707] (imputed) 0 hormone measurement http://www.ebi.ac.uk/efo/EFO_0004730 GCST90102246 Genome-wide genotyping array 2022-06-22 35316565 Helenius M 2022-03-22 Pediatr Blood Cancer www.ncbi.nlm.nih.gov/pubmed/35316565 Characteristics of white blood cell count in acute lymphoblastic leukemia: A COST LEGEND phenotype-genotype study. Log white blood cell count in acute lymphoblastic leukemia 1,698 European ancestry individuals NA Illumina [2146366] 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90104779 Genome-wide genotyping array 2022-06-22 35316565 Helenius M 2022-03-22 Pediatr Blood Cancer www.ncbi.nlm.nih.gov/pubmed/35316565 Characteristics of white blood cell count in acute lymphoblastic leukemia: A COST LEGEND phenotype-genotype study. Spline residuals of log white blood cell count in acute lymphoblastic leukemia 1,698 European ancestry individuals NA Illumina [2146366] 7 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90104780 Genome-wide genotyping array 2022-04-06 34794066 Wills C 2021-11-15 Eur J Cancer www.ncbi.nlm.nih.gov/pubmed/34794066 A genome-wide search for determinants of survival in 1926 patients with advanced colorectal cancer with follow-up in over 22,000 patients. Overall survival in advanced colorectal cancer 1,926 unknown and European ancestry individuals 22,639 unknown and European ancestry individuals Affymetrix [2900000] (imputed) 17 colorectal cancer, overall survival http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90101725 Genome-wide genotyping array 2022-06-14 34962275 Lin WY 2021-12-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34962275 Genome-wide association study for four measures of epigenetic age acceleration and two epigenetic surrogate markers using DNA methylation data from Taiwan biobank. DNA methylation PhenoAge acceleration 2,309 East Asian ancestry individuals NA Affymetrix [7433014] (imputed) 0 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104401 Genome-wide genotyping array 2022-06-14 34962275 Lin WY 2021-12-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34962275 Genome-wide association study for four measures of epigenetic age acceleration and two epigenetic surrogate markers using DNA methylation data from Taiwan biobank. DNA methylation-estimated granulocyte proportions 2,309 East Asian ancestry individuals NA Affymetrix [7433014] (imputed) 1 obsolete aging, granulocyte count http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0007987 GCST90104402 Genome-wide genotyping array 2022-06-14 34962275 Lin WY 2021-12-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34962275 Genome-wide association study for four measures of epigenetic age acceleration and two epigenetic surrogate markers using DNA methylation data from Taiwan biobank. DNA methylation GrimAge acceleration 2,309 East Asian ancestry individuals NA Affymetrix [7433014] (imputed) 1 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104403 Genome-wide genotyping array 2022-06-14 34962275 Lin WY 2021-12-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34962275 Genome-wide association study for four measures of epigenetic age acceleration and two epigenetic surrogate markers using DNA methylation data from Taiwan biobank. Intrinsic epigenetic age acceleration 2,309 East Asian ancestry individuals NA Affymetrix [7433014] (imputed) 2 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104404 Genome-wide genotyping array 2022-06-14 34962275 Lin WY 2021-12-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34962275 Genome-wide association study for four measures of epigenetic age acceleration and two epigenetic surrogate markers using DNA methylation data from Taiwan biobank. DNA methylation Hannum age acceleration 2,309 East Asian ancestry individuals NA Affymetrix [7433014] (imputed) 3 obsolete aging, epigenetic status http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0000473 GCST90104405 Genome-wide genotyping array 2022-06-14 34962275 Lin WY 2021-12-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/34962275 Genome-wide association study for four measures of epigenetic age acceleration and two epigenetic surrogate markers using DNA methylation data from Taiwan biobank. DNA methylation-estimated plasminogen activator inhibitor-1 levels 2,309 East Asian ancestry individuals NA Affymetrix [7433014] (imputed) 1 obsolete aging, plasminogen activator inhibitor 1 measurement http://purl.obolibrary.org/obo/GO_0007568, http://www.ebi.ac.uk/efo/EFO_0004792 GCST90104406 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-3781|aerobic respiration I (cytochrome c)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026793 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-4984|urea cycle) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026794 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5005|biotin biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 31 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026795 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5022|4-aminobutanoate degradation V) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026796 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5100|pyruvate fermentation to acetate and lactate II) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026797 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5101|L-isoleucine biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026798 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5103|L-isoleucine biosynthesis III) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026799 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5104|L-isoleucine biosynthesis IV) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026800 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5121|superpathway of geranylgeranyl diphosphate biosynthesis II (via MEP)) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026801 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5154|L-arginine biosynthesis III (via N-acetyl-L-citrulline)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026802 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5177|glutaryl-CoA degradation) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026803 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5180|toluene degradation I (aerobic) (via o-cresol)) 315 Chinese ancestry individuals NA Illumina [492582] 49 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026804 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5182|toluene degradation II (aerobic) (via 4-methylcatechol)) 315 Chinese ancestry individuals NA Illumina [492582] 31 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026805 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5188|tetrapyrrole biosynthesis I (from glutamate)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026806 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5189|tetrapyrrole biosynthesis II (from glycine)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026807 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5265|peptidoglycan biosynthesis II (staphylococci)) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026808 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5304|superpathway of sulfur oxidation (Acidianus ambivalens)) 315 Chinese ancestry individuals NA Illumina [492582] 15 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026809 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5345|superpathway of L-methionine biosynthesis (by sulfhydrylation)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026810 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5347|superpathway of L-methionine biosynthesis (transsulfuration)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026811 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5384|sucrose degradation IV (sucrose phosphorylase)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026812 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5415|catechol degradation I (meta-cleavage pathway)) 315 Chinese ancestry individuals NA Illumina [492582] 39 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026813 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5484|glycolysis II (from fructose 6-phosphate)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026814 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5505|L-glutamate and L-glutamine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026815 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5507|adenosylcobalamin biosynthesis I (early cobalt insertion)) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026816 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-5509|adenosylcobalamin biosynthesis from cobyrinate a,c-diamide I) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026817 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P221-PWY|octane oxidation) 315 Chinese ancestry individuals NA Illumina [492582] 23 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026768 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P23-PWY|reductive TCA cycle I) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026769 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P381-PWY|adenosylcobalamin biosynthesis II (late cobalt incorporation)) 315 Chinese ancestry individuals NA Illumina [492582] 15 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026770 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P42-PWY|incomplete reductive TCA cycle) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026771 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P441-PWY|superpathway of N-acetylneuraminate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026772 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P461-PWY|hexitol fermentation to lactate, formate, ethanol and acetate) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026773 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (P562-PWY|myo-inositol degradation I) 315 Chinese ancestry individuals NA Illumina [492582] 21 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026774 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PANTO-PWY|phosphopantothenate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026775 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PANTOSYN-PWY|pantothenate and coenzyme A biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026776 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PENTOSE-P-PWY|pentose phosphate pathway) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026777 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PEPTIDOGLYCANSYN-PWY|peptidoglycan biosynthesis I (meso-diaminopimelate containing)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026778 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PHOSLIPSYN-PWY|superpathway of phospholipid biosynthesis I (bacteria)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026779 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (POLYAMINSYN3-PWY|superpathway of polyamine biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026780 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (POLYAMSYN-PWY|superpathway of polyamine biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026781 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (POLYISOPRENSYN-PWY|polyisoprenoid biosynthesis (E. coli)) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026782 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PPGPPMET-PWY|ppGpp biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026783 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PROTOCATECHUATE-ORTHO-CLEAVAGE-PWY|protocatechuate degradation II (ortho-cleavage pathway)) 315 Chinese ancestry individuals NA Illumina [492582] 27 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026784 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PRPP-PWY|superpathway of histidine, purine, and pyrimidine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026785 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-1269|CMP-3-deoxy-D-manno-octulosonate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026786 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-1622|formaldehyde assimilation I (serine pathway)) 315 Chinese ancestry individuals NA Illumina [492582] 40 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026787 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-181|photorespiration) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026788 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-1861|formaldehyde assimilation II (RuMP Cycle)) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026789 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-2941|L-lysine biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026790 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-2942|L-lysine biosynthesis III) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026791 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-3001|superpathway of L-isoleucine biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026792 Genome-wide genotyping array 2022-06-07 33583074 Le Guen Y 2021-03-06 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/33583074 Common X-Chromosome Variants Are Associated with Parkinson Disease Risk. Parkinson's disease 3,500 European ancestry female cases, 1,828 European ancestry female proxy cases, 297,580 European ancestry controls 535 European ancestry cases, 1,317 European ancestry controls Affymetrix, Illumina [1376254] (imputed) 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90104085 Genome-wide genotyping array, Exome genotyping array [NeuroX Array | HumanHap550 | HumanOmni1-Quad | 610 k Quad | 1.2 M | Axiom Array | NeuroX | 660 W | Infinium OmniExpress-24 | HiSeq XTen], Genome-wide sequencing [NeuroX Array | HumanHap550 | HumanOmni1-Quad | 610 k Quad | 1.2 M | Axiom Array | NeuroX | 660 W | Infinium OmniExpress-24 | HiSeq XTen] 2022-06-07 33583074 Le Guen Y 2021-03-06 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/33583074 Common X-Chromosome Variants Are Associated with Parkinson Disease Risk. Parkinson's disease 6,451 European ancestry male cases, 3,551 European ancestry male proxy cases, 251,229 European ancestry controls 1,027 European ancestry cases, 1,147 European ancestry controls Affymetrix, Illumina [1376254] (imputed) 2 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90104086 Genome-wide genotyping array, Exome genotyping array [NeuroX Array | HumanHap550 | HumanOmni1-Quad | 610 k Quad | 1.2 M | Axiom Array | NeuroX | 660 W | Infinium OmniExpress-24 | HiSeq XTen], Genome-wide sequencing [NeuroX Array | HumanHap550 | HumanOmni1-Quad | 610 k Quad | 1.2 M | Axiom Array | NeuroX | 660 W | Infinium OmniExpress-24 | HiSeq XTen] 2022-06-07 33583074 Le Guen Y 2021-03-06 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/33583074 Common X-Chromosome Variants Are Associated with Parkinson Disease Risk. Parkinson's disease 11,142 European ancestry cases, 5,379 European ancestry proxy cases, 547,618 European ancestry controls 1,561 European ancestry cases, 2,465 European ancestry controls Affymetrix, Illumina [1376254] (imputed) 4 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90104087 Genome-wide genotyping array, Exome genotyping array [NeuroX Array | HumanHap550 | HumanOmni1-Quad | 610 k Quad | 1.2 M | Axiom Array | NeuroX | 660 W | Infinium OmniExpress-24 | HiSeq XTen], Genome-wide sequencing [NeuroX Array | HumanHap550 | HumanOmni1-Quad | 610 k Quad | 1.2 M | Axiom Array | NeuroX | 660 W | Infinium OmniExpress-24 | HiSeq XTen] 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Colorectal cancer 835 Basque ancestry cases, 940 Basque ancestry controls NA Illumina [5399385] (imputed) 5 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90162552 Genome-wide genotyping array 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Right colon cancer 170 Basque ancestry cases, 940 Basque ancestry controls NA Illumina [5390111] (imputed) 16 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90162553 Genome-wide genotyping array 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Left colon cancer 219 Basque ancestry cases, 940 Basque ancestry controls NA Illumina [5394955] (imputed) 7 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90162554 Genome-wide genotyping array 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Rectal cancer 235 Basque ancestry cases, 940 Basque ancestry controls NA Illumina [5394721] (imputed) 10 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90162555 Genome-wide genotyping array 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Left colon cancer vs right colon cancer 219 Basque ancestry cases, 170 Basque ancestry controls NA Illumina [5399981] (imputed) 2 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90179121 Genome-wide genotyping array 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Rectal cancer vs colon cancer 235 Basque ancestry cases, 389 Basque ancestry controls NA Illumina [5399981] (imputed) 3 rectum cancer, colonic neoplasm http://www.ebi.ac.uk/efo/EFO_1000657, http://www.ebi.ac.uk/efo/EFO_0004288 GCST90179122 Genome-wide genotyping array 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Colorectal cancer vs inflammatory bowel disease 835 Basque ancestry cases, 492 Basque ancestry controls NA Illumina [5399981] (imputed) 11 colorectal cancer, inflammatory bowel disease http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90179123 Genome-wide genotyping array 2022-10-18 36077729 Garcia-Etxebarria K 2022-08-29 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/36077729 Performance of the Use of Genetic Information to Assess the Risk of Colorectal Cancer in the Basque Population. Colorectal cancer vs inflammatory bowel disease or controls 835 Basque ancestry cases, 1,432 Basque ancestry controls NA Illumina [5399981] (imputed) 9 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90179124 Genome-wide genotyping array 2022-06-23 35321643 Fang F 2022-03-23 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35321643 Sex-specific genetic modifiers identified susceptibility of cold stored red blood cells to osmotic hemolysis. Osmotic hemolysis of cold stored red blood cells 3,975 European ancestry men, 694 African American men, 807 Asian ancestry men, 378 Hispanic men, 274 men NA NR [NR] (imputed) 4 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST90104789 Genome-wide genotyping array 2022-06-23 35321643 Fang F 2022-03-23 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35321643 Sex-specific genetic modifiers identified susceptibility of cold stored red blood cells to osmotic hemolysis. Osmotic hemolysis of cold stored red blood cells 3,789 European ancestry women, 773 African American women, 654 Asian ancestry women, 568 Hispanic women, 319 women NA NR [NR] (imputed) 3 hemolysis http://www.ebi.ac.uk/efo/EFO_0009473 GCST90104790 Genome-wide genotyping array 2022-06-23 35321643 Fang F 2022-03-23 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35321643 Sex-specific genetic modifiers identified susceptibility of cold stored red blood cells to osmotic hemolysis. Osmotic hemolysis of cold stored red blood cells x sex interaction (2df) 7,764 European ancestry individuals, 1,467 African American individuals, 1,461 Asian ancestry individuals, 946 Hispanic individuals, 593 individuals NA NR [NR] (imputed) 0 sex interaction measurement, hemolysis http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0009473 GCST90104791 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ulcerative colitis 314 East Asian ancestry cases, 178,375 East Asian ancestry controls NA Illumina [13429945] (imputed) 1 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90018713 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Uterine fibroids 14,475 East Asian ancestry cases, 65,733 East Asian ancestry controls NA Illumina [13401454] (imputed) 20 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90018714 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Urolithiasis 11,699 East Asian ancestry cases, 167,027 East Asian ancestry controls NA Illumina [13429980] (imputed) 19 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90018715 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Urticaria 9,893 East Asian ancestry cases, 162,190 East Asian ancestry controls NA Illumina [13429081] (imputed) 2 urticaria http://www.ebi.ac.uk/efo/EFO_0005531 GCST90018716 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Uterine prolapse 423 East Asian ancestry cases, 82,338 East Asian ancestry controls NA Illumina [13403071] (imputed) 0 uterine prolapse http://www.ebi.ac.uk/efo/EFO_1001864 GCST90018717 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Uveitis 125 East Asian ancestry cases, 174,600 East Asian ancestry controls NA Illumina [13429518] (imputed) 0 uveitis http://www.ebi.ac.uk/efo/EFO_1001231 GCST90018718 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Varicose veins 474 East Asian ancestry cases, 178,252 East Asian ancestry controls NA Illumina [13429980] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90018719 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ventricular arrhythmia 1,673 East Asian ancestry cases, 155,540 East Asian ancestry controls NA Illumina [13426630] (imputed) 1 Ventricular arrhythmia http://purl.obolibrary.org/obo/HP_0004308 GCST90018720 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Zoster infection 2,209 East Asian ancestry cases, 166,603 East Asian ancestry controls NA Illumina [13428120] (imputed) 1 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST90018721 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum alkaline phosphatase levels 118,886 East Asian ancestry individuals NA Illumina [13474352] (imputed) 37 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90018722 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Alanine aminotransferase levels 150,545 East Asian ancestry individuals NA Illumina [13478866] (imputed) 32 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90018723 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Aspartate aminotransferase levels 150,068 East Asian ancestry individuals NA Illumina [13478956] (imputed) 32 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90018724 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum albumin levels 120,539 East Asian ancestry individuals NA Illumina [13474682] (imputed) 26 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90018725 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Basophil count 91,908 East Asian ancestry individuals NA Illumina [13469940] (imputed) 37 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90018726 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Body mass index 163,835 East Asian ancestry individuals NA Illumina [13479178] (imputed) 89 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90018727 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Blood urea nitrogen levels 148,767 East Asian ancestry individuals NA Illumina [13478792] (imputed) 44 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST90018728 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Weight 165,419 East Asian ancestry individuals NA Illumina [13479924] (imputed) 157 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90018729 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. C-reactive protein 83,025 East Asian ancestry individuals NA Illumina [13470202] (imputed) 5 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90018730 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Calcium levels 83,980 East Asian ancestry individuals NA Illumina [13468899] (imputed) 15 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90018731 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Diastolic blood pressure 145,515 East Asian ancestry individuals NA Illumina [13477770] (imputed) 24 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90018732 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Eosinophil counts 93,063 East Asian ancestry individuals NA Illumina [13470073] (imputed) 38 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90018733 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gamma glutamyl transpeptidase 133,471 East Asian ancestry individuals NA Illumina [13476165] (imputed) 52 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90018734 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Glucose levels 133,336 East Asian ancestry individuals NA Illumina [13476509] (imputed) 17 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90018735 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. HDL cholesterol 74,970 East Asian ancestry individuals NA Illumina [13465896] (imputed) 41 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90018736 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hemoglobin 152,447 East Asian ancestry individuals NA Illumina [13478948] (imputed) 45 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90018737 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at birth 28,681 European ancestry individuals NA Illumina [9200000] (imputed) 9 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104629 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 6 weeks old 18,333 European ancestry individuals NA Illumina [9200000] (imputed) 5 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104630 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 3 months old 14,064 European ancestry individuals NA Illumina [9200000] (imputed) 20 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104631 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 6 months old 11,095 European ancestry individuals NA Illumina [9200000] (imputed) 21 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104632 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 8 months old 24,302 European ancestry individuals NA Illumina [9200000] (imputed) 23 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104633 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 1 year old 24,551 European ancestry individuals NA Illumina [9200000] (imputed) 24 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104634 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 1.5 years old 21,871 European ancestry individuals NA Illumina [9200000] (imputed) 16 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104635 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 2 years old 21,831 European ancestry individuals NA Illumina [9200000] (imputed) 13 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104636 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 3 years old 21,514 European ancestry individuals NA Illumina [9200000] (imputed) 6 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104637 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 5 years old 16,902 European ancestry individuals NA Illumina [9200000] (imputed) 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104638 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 7 years old 17,212 European ancestry individuals NA Illumina [9200000] (imputed) 7 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104639 Genome-wide genotyping array 2022-06-20 35315439 Helgeland O 2022-03-21 Nat Metab www.ncbi.nlm.nih.gov/pubmed/35315439 Characterization of the genetic architecture of infant and early childhood body mass index. BMI at 8 years old 14,280 European ancestry individuals NA Illumina [9200000] (imputed) 6 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90104640 Genome-wide genotyping array 2022-10-14 35942816 Lehtisalo M 2022-08-09 Br J Clin Pharmacol www.ncbi.nlm.nih.gov/pubmed/35942816 A Comprehensive Pharmacogenomic Study Indicates Roles for SLCO1B1, ABCG2, and SLCO2B1 in Rosuvastatin Pharmacokinetics. Peak plasma concentration of rosuvastatin 159 Finnish ancestry individuals NA Illumina [NR] 0 response to rosuvastatin http://www.ebi.ac.uk/efo/EFO_0021896 GCST90140956 Genome-wide genotyping array 2022-10-14 35942816 Lehtisalo M 2022-08-09 Br J Clin Pharmacol www.ncbi.nlm.nih.gov/pubmed/35942816 A Comprehensive Pharmacogenomic Study Indicates Roles for SLCO1B1, ABCG2, and SLCO2B1 in Rosuvastatin Pharmacokinetics. Plasma concentration-time curve of rosuvastatin 159 Finnish ancestry individuals NA Illumina [NR] 0 response to rosuvastatin http://www.ebi.ac.uk/efo/EFO_0021896 GCST90140957 Genome-wide genotyping array 2022-10-14 35942816 Lehtisalo M 2022-08-09 Br J Clin Pharmacol www.ncbi.nlm.nih.gov/pubmed/35942816 A Comprehensive Pharmacogenomic Study Indicates Roles for SLCO1B1, ABCG2, and SLCO2B1 in Rosuvastatin Pharmacokinetics. Elimination half-life of rosuvastatin 159 Finnish ancestry individuals NA Illumina [NR] 0 response to rosuvastatin http://www.ebi.ac.uk/efo/EFO_0021896 GCST90140958 Genome-wide genotyping array 2022-10-14 35942816 Lehtisalo M 2022-08-09 Br J Clin Pharmacol www.ncbi.nlm.nih.gov/pubmed/35942816 A Comprehensive Pharmacogenomic Study Indicates Roles for SLCO1B1, ABCG2, and SLCO2B1 in Rosuvastatin Pharmacokinetics. Peak plasma concentration of rosuvastatin 247 Finnish ancestry individuals NA Illumina [NR] 1 response to rosuvastatin http://www.ebi.ac.uk/efo/EFO_0021896 GCST90140959 Genome-wide genotyping array 2022-10-14 35942816 Lehtisalo M 2022-08-09 Br J Clin Pharmacol www.ncbi.nlm.nih.gov/pubmed/35942816 A Comprehensive Pharmacogenomic Study Indicates Roles for SLCO1B1, ABCG2, and SLCO2B1 in Rosuvastatin Pharmacokinetics. Plasma concentration-time curve of rosuvastatin 247 Finnish ancestry individuals NA Illumina [NR] 1 response to rosuvastatin http://www.ebi.ac.uk/efo/EFO_0021896 GCST90140960 Genome-wide genotyping array 2022-10-14 35942816 Lehtisalo M 2022-08-09 Br J Clin Pharmacol www.ncbi.nlm.nih.gov/pubmed/35942816 A Comprehensive Pharmacogenomic Study Indicates Roles for SLCO1B1, ABCG2, and SLCO2B1 in Rosuvastatin Pharmacokinetics. Elimination half-life of rosuvastatin 247 Finnish ancestry individuals NA Illumina [NR] 0 response to rosuvastatin http://www.ebi.ac.uk/efo/EFO_0021896 GCST90140961 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hemoglobin A1c levels 71,221 East Asian ancestry individuals NA Illumina [13466143] (imputed) 25 hemoglobin A1 measurement http://www.ebi.ac.uk/efo/EFO_0007629 GCST90018738 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Height 165,056 East Asian ancestry individuals NA Illumina [13479295] (imputed) 388 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90018739 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hematocrit 153,015 East Asian ancestry individuals NA Illumina [13478961] (imputed) 51 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90018740 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. LDL cholesterol 72,866 East Asian ancestry individuals NA Illumina [13461863] (imputed) 29 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90018741 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Lymphocyte count 95,717 East Asian ancestry individuals NA Illumina [13471431] (imputed) 29 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90018742 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean arterial pressure 145,502 East Asian ancestry individuals NA Illumina [13477767] (imputed) 35 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST90018743 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean corpuscular hemoglobin 128,028 East Asian ancestry individuals NA Illumina [13476299] (imputed) 122 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90018744 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean corpuscular hemoglobin concentration 135,482 East Asian ancestry individuals NA Illumina [13477028] (imputed) 48 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90018745 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean corpuscular volume 129,832 East Asian ancestry individuals NA Illumina [13476266] (imputed) 134 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90018746 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Monocyte count 95,119 East Asian ancestry individuals NA Illumina [13471440] (imputed) 53 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90018747 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Neutrophil count 82,810 East Asian ancestry individuals NA Illumina [13467171] (imputed) 29 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90018748 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Platelet count 148,623 East Asian ancestry individuals NA Illumina [13478928] (imputed) 136 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90018749 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pulse pressure 145,445 East Asian ancestry individuals NA Illumina [13477769] (imputed) 21 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90018750 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Red blood cell count 153,512 East Asian ancestry individuals NA Illumina [13479135] (imputed) 97 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90018751 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Systolic blood pressure 145,505 East Asian ancestry individuals NA Illumina [13477770] (imputed) 37 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90018752 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Total bilirubin levels 124,341 East Asian ancestry individuals NA Illumina [13476323] (imputed) 15 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90018753 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Total cholesterol levels 135,808 East Asian ancestry individuals NA Illumina [13476599] (imputed) 41 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90018754 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Triglycerides 111,667 East Asian ancestry individuals NA Illumina [13471903] (imputed) 28 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90018755 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum total protein levels 133,321 East Asian ancestry individuals NA Illumina [13477433] (imputed) 38 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90018756 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum uric acid levels 129,405 East Asian ancestry individuals NA Illumina [13475706] (imputed) 40 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90018757 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. White blood cell count 154,355 East Asian ancestry individuals NA Illumina [13479091] (imputed) 75 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90018758 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum creatinine levels 150,266 East Asian ancestry individuals NA Illumina [13478778] (imputed) 87 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90018759 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (drugs for peptic ulcer and gastro-oesophageal reflux disease) 53,363 East Asian ancestry cases, 125,363 East Asian ancestry controls NA Illumina [13429980] (imputed) 1 Peptic ulcer and gastro-oesophageal reflux disease (GORD) drug use measurement http://www.ebi.ac.uk/efo/EFO_0009923 GCST90018760 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (drugs used in diabetes) 30,515 East Asian ancestry cases, 148,211 East Asian ancestry controls NA Illumina [13134967] (imputed) 65 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90018761 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antithrombotic agents) 54,220 East Asian ancestry cases, 124,506 East Asian ancestry controls NA Illumina [13429980] (imputed) 20 Antithrombotic agent use measurement http://www.ebi.ac.uk/efo/EFO_0009925 GCST90018762 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Endometrial cancer 2,188 European ancestry cases, 237,839 European ancestry controls, 1,200 East Asian ancestry cases, 60,614 East Asian ancestry controls NA Affymetrix, Illumina [25777865] (imputed) 2 endometrial carcinoma http://www.ebi.ac.uk/efo/EFO_1001512 GCST90018838 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Endometriosis 4,511 European ancestry cases, 227,260 European ancestry controls, 1,786 East Asian ancestry cases, 80,975 East Asian ancestry controls NA Affymetrix, Illumina [25734875] (imputed) 7 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90018839 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Epilepsy 4,382 European ancestry cases, 453,928 European ancestry controls, 2,466 East Asian ancestry cases, 175,788 East Asian ancestry controls NA Affymetrix, Illumina [25841675] (imputed) 2 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90018840 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Esophageal cancer 998 European ancestry cases, 475,308 European ancestry controls, 1,388 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Affymetrix, Illumina [25843129] (imputed) 4 esophageal carcinoma http://www.ebi.ac.uk/efo/EFO_0002916 GCST90018841 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Esophageal varix 2,135 European ancestry cases, 434,019 European ancestry controls, 264 East Asian ancestry cases, 177,516 East Asian ancestry controls NA Affymetrix, Illumina [25840700] (imputed) 2 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90018842 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Bell's palsy 1,894 European ancestry cases, 461,346 European ancestry controls, 343 East Asian ancestry cases, 178,191 East Asian ancestry controls NA Affymetrix, Illumina [25842617] (imputed) 1 Bell's palsy http://www.ebi.ac.uk/efo/EFO_0007167 GCST90018843 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Febrile seizures 2,366 European ancestry cases, 342,965 European ancestry controls, 574 East Asian ancestry cases, 175,272 East Asian ancestry controls NA Affymetrix, Illumina [20457414] (imputed) 0 Seizure http://purl.obolibrary.org/obo/HP_0001250 GCST90018844 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Food allergy 182 European ancestry cases, 350,904 European ancestry controls, 3,777 East Asian ancestry cases, 165,939 East Asian ancestry controls NA Affymetrix, Illumina [20457211] (imputed) 0 food allergy measurement http://www.ebi.ac.uk/efo/EFO_0007016 GCST90018845 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gallbladder polyp 458 European ancestry cases, 340,083 European ancestry controls, 843 East Asian ancestry cases, 167,459 East Asian ancestry controls NA Affymetrix, Illumina [20456458] (imputed) 3 polyp of gallbladder http://purl.obolibrary.org/obo/MONDO_0021416 GCST90018846 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Graves' disease 1,678 European ancestry cases, 456,942 European ancestry controls, 2,809 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Affymetrix, Illumina [25841587] (imputed) 25 Graves disease http://www.ebi.ac.uk/efo/EFO_0004237 GCST90018847 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastroesophageal reflux disease 32,957 European ancestry cases, 434,296 European ancestry controls, 948 East Asian ancestry cases, 177,516 East Asian ancestry controls NA Affymetrix, Illumina [25843127] (imputed) 2 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90018848 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastric cancer 1,029 European ancestry cases, 475,087 European ancestry controls, 7,921 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Affymetrix, Illumina [25843697] (imputed) 7 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90018849 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastric polyp 6,155 European ancestry cases, 341,871 European ancestry controls, 1,337 East Asian ancestry cases, 158,249 East Asian ancestry controls NA Affymetrix, Illumina [20456140] (imputed) 5 stomach polyp http://purl.obolibrary.org/obo/MONDO_0008277 GCST90018850 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gastric ulcer 6,293 European ancestry cases, 467,985 European ancestry controls, 12,650 East Asian ancestry cases, 161,227 East Asian ancestry controls NA Affymetrix, Illumina [25842546] (imputed) 5 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90018851 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Glaucoma 10,411 European ancestry cases, 474,568 European ancestry controls, 8,448 East Asian ancestry cases, 168,903 East Asian ancestry controls NA Affymetrix, Illumina [25844939] (imputed) 37 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90018852 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Goiter 2,711 European ancestry cases, 456,942 European ancestry controls, 1,127 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Affymetrix, Illumina [25841617] (imputed) 16 goiter http://www.ebi.ac.uk/efo/EFO_0004283 GCST90018853 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Acute hepatitis A infection 69 European ancestry cases, 351,740 European ancestry controls, 261 East Asian ancestry cases, 166,603 East Asian ancestry controls NA Affymetrix, Illumina [20456890] (imputed) 0 hepatitis A virus infection http://www.ebi.ac.uk/efo/EFO_0007305 GCST90018854 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hashimoto thyroiditis 15,654 European ancestry cases, 379,986 European ancestry controls, 537 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Affymetrix, Illumina [25797652] (imputed) 14 Hashimoto's thyroiditis http://www.ebi.ac.uk/efo/EFO_0003779 GCST90018855 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Head injury 7,746 European ancestry cases, 349,912 European ancestry controls, 2,440 East Asian ancestry cases, 176,286 East Asian ancestry controls NA Affymetrix, Illumina [20458276] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90018856 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hearing loss, difficulty in hearing 14,654 European ancestry cases, 474,839 European ancestry controls, 3,400 East Asian ancestry cases, 175,326 East Asian ancestry controls NA Affymetrix, Illumina [25845022] (imputed) 4 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90018857 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hepatic cancer 379 European ancestry cases, 475,259 European ancestry controls, 2,122 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Affymetrix, Illumina [25843189] (imputed) 4 liver neoplasm http://www.ebi.ac.uk/efo/EFO_1001513 GCST90018858 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Herpes infection 313 European ancestry cases, 351,740 European ancestry controls, 772 East Asian ancestry cases, 166,603 East Asian ancestry controls NA Affymetrix, Illumina [20456945] (imputed) 0 Herpes simplex infection http://www.ebi.ac.uk/efo/EFO_1002022 GCST90018859 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hyperthyroidism 3,557 European ancestry cases, 456,942 European ancestry controls, 994 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Affymetrix, Illumina [25841580] (imputed) 11 hyperthyroidism http://www.ebi.ac.uk/efo/EFO_0009189 GCST90018860 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hypertrophic cardiomyopathy 507 European ancestry cases, 489,220 European ancestry controls, 383 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Affymetrix, Illumina [25845237] (imputed) 6 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST90018861 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hypothyroidism 30,155 European ancestry cases, 379,986 European ancestry controls, 1,114 East Asian ancestry cases, 172,656 East Asian ancestry controls NA Affymetrix, Illumina [25801083] (imputed) 77 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90018862 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ovarian cancer 1,588 European ancestry cases, 244,932 European ancestry controls, 843 East Asian ancestry cases, 60,614 East Asian ancestry controls NA Affymetrix, Illumina [25778302] (imputed) 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90018888 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ovarian cyst 10,847 European ancestry cases, 207,622 European ancestry controls, 2,896 East Asian ancestry cases, 79,865 East Asian ancestry controls NA Affymetrix, Illumina [25752875] (imputed) 5 Ovarian cyst http://purl.obolibrary.org/obo/HP_0000138 GCST90018889 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Peripheral artery disease 7,114 European ancestry cases, 475,964 European ancestry controls, 4,112 East Asian ancestry cases, 173,601 East Asian ancestry controls NA Affymetrix, Illumina [25844651] (imputed) 7 peripheral arterial disease http://www.ebi.ac.uk/efo/EFO_0004265 GCST90018890 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Polymyositis 44 European ancestry cases, 350,228 European ancestry controls, 58 East Asian ancestry cases, 175,599 East Asian ancestry controls NA Affymetrix, Illumina [20457706] (imputed) 1 polymyositis http://www.ebi.ac.uk/efo/EFO_0003063 GCST90018891 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pulmonary tuberculosis 895 European ancestry cases, 476,491 European ancestry controls, 7,800 East Asian ancestry cases, 170,871 East Asian ancestry controls NA Affymetrix, Illumina [25844658] (imputed) 1 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90018892 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pancreatic cancer 1,196 European ancestry cases, 475,049 European ancestry controls, 499 East Asian ancestry cases, 159,201 East Asian ancestry controls NA Affymetrix, Illumina [25843042] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90018893 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Parkinson's disease 2,638 European ancestry cases, 477,380 European ancestry controls, 340 East Asian ancestry cases, 175,788 East Asian ancestry controls NA Affymetrix, Illumina [25844586] (imputed) 2 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90018894 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pediatric asthma 27,712 European ancestry cases, 411,131 European ancestry controls, 547 East Asian ancestry cases, 161,803 East Asian ancestry controls NA Affymetrix, Illumina [25832605] (imputed) 35 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST90018895 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pericarditis 1,795 European ancestry cases, 453,370 European ancestry controls, 89 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Affymetrix, Illumina [25837988] (imputed) 0 pericarditis http://www.ebi.ac.uk/efo/EFO_0007427 GCST90018896 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Periodontal disease 1,740 European ancestry cases, 347,186 European ancestry controls, 9,560 East Asian ancestry cases, 169,166 East Asian ancestry controls NA Affymetrix, Illumina [20457829] (imputed) 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90018897 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pharyngeal and laryngeal cancer 329 European ancestry cases, 355,235 European ancestry controls, 300 East Asian ancestry cases, 178,426 East Asian ancestry controls NA Affymetrix, Illumina [20458189] (imputed) 0 pharynx cancer, laryngeal carcinoma http://www.ebi.ac.uk/efo/EFO_0005577, http://purl.obolibrary.org/obo/MONDO_0002358 GCST90018898 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pleurisy 8,528 European ancestry cases, 475,987 European ancestry controls, 541 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Affymetrix, Illumina [25844732] (imputed) 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90018899 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pneumoconiosis 433 European ancestry cases, 478,607 European ancestry controls, 85 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Affymetrix, Illumina [25844546] (imputed) 0 pneumoconiosis http://purl.obolibrary.org/obo/MONDO_0015926 GCST90018900 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pneumonia 16,887 European ancestry cases, 463,412 European ancestry controls, 7,423 East Asian ancestry cases, 171,303 East Asian ancestry controls NA Affymetrix, Illumina [25843326] (imputed) 1 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90018901 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pneumothorax 1,747 European ancestry cases, 475,987 European ancestry controls, 692 East Asian ancestry cases, 176,298 East Asian ancestry controls NA Affymetrix, Illumina [25844290] (imputed) 2 pneumothorax http://purl.obolibrary.org/obo/MONDO_0002076 GCST90018902 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pollinosis 2,894 European ancestry cases, 472,484 European ancestry controls, 18,593 East Asian ancestry cases, 153,666 East Asian ancestry controls NA Affymetrix, Illumina [25844049] (imputed) 5 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90018903 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Polycystic kidney disease 424 European ancestry cases, 355,431 European ancestry controls, 510 East Asian ancestry cases, 178,216 East Asian ancestry controls NA Affymetrix, Illumina [20458172] (imputed) 0 Polycystic Kidney Disease http://www.ebi.ac.uk/efo/EFO_0008620 GCST90018904 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Prostate cancer 11,599 European ancestry cases, 199,628 European ancestry controls, 5,672 East Asian ancestry cases, 84,660 East Asian ancestry controls NA Affymetrix, Illumina [25775424] (imputed) 59 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90018905 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Preeclampsia 2,355 European ancestry cases, 264,887 European ancestry controls, 123 East Asian ancestry cases, 81,962 East Asian ancestry controls NA Affymetrix, Illumina [25813232] (imputed) 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90018906 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Psoriasis vulgaris 5,072 European ancestry cases, 478,102 European ancestry controls, 206 East Asian ancestry cases, 172,289 East Asian ancestry controls NA Affymetrix, Illumina [25844455] (imputed) 10 psoriasis vulgaris http://www.ebi.ac.uk/efo/EFO_1001494 GCST90018907 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pulmonary fibrosis 1,566 European ancestry cases, 467,560 European ancestry controls, 126 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Affymetrix, Illumina [25843031] (imputed) 6 pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0009448 GCST90018908 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pyelonephritis 7,992 European ancestry cases, 454,495 European ancestry controls, 1,811 East Asian ancestry cases, 175,288 East Asian ancestry controls NA Affymetrix, Illumina [25843519] (imputed) 0 pyelonephritis http://www.ebi.ac.uk/efo/EFO_1001141 GCST90018909 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Rheumatoid arthritis 8,255 European ancestry cases, 409,001 European ancestry controls, 5,348 East Asian ancestry cases, 173,268 East Asian ancestry controls NA Affymetrix, Illumina [25835038] (imputed) 21 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90018910 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Retinal detachment 6,591 European ancestry cases, 470,440 European ancestry controls, 1,389 East Asian ancestry cases, 168,903 East Asian ancestry controls NA Affymetrix, Illumina [25843609] (imputed) 4 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90018911 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Retinitis pigmentosa 121 European ancestry cases, 126,333 European ancestry controls, 155 East Asian ancestry cases, 168,903 East Asian ancestry controls NA Illumina [23539365] (imputed) 5 retinitis pigmentosa http://purl.obolibrary.org/obo/MONDO_0019200 GCST90018912 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Carpal tunnel syndrome 18,855 European ancestry cases, 461,346 European ancestry controls, 192 East Asian ancestry cases, 178,534 East Asian ancestry controls NA Affymetrix, Illumina [25844227] (imputed) 16 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90018813 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cataracts 39,519 European ancestry cases, 452,358 European ancestry controls, 38,194 East Asian ancestry cases, 140,532 East Asian ancestry controls NA Affymetrix, Illumina [25845331] (imputed) 32 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90018814 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cerebral aneurysm 945 European ancestry cases, 472,738 European ancestry controls, 3,132 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Affymetrix, Illumina [25841674] (imputed) 6 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90018815 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Unruptured cerebral aneurysm 945 European ancestry cases, 472,738 European ancestry controls, 91 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Affymetrix, Illumina [25841390] (imputed) 2 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST90018816 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cervical cancer 909 European ancestry cases, 238,249 European ancestry controls, 967 East Asian ancestry cases, 60,614 East Asian ancestry controls NA Affymetrix, Illumina [25777760] (imputed) 1 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90018817 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cholecystitis 9,820 European ancestry cases, 461,431 European ancestry controls, 1,860 East Asian ancestry cases, 168,253 East Asian ancestry controls NA Affymetrix, Illumina [25842273] (imputed) 13 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90018818 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cholelithiasis 26,122 European ancestry cases, 461,431 European ancestry controls, 9,305 East Asian ancestry cases, 168,253 East Asian ancestry controls NA Affymetrix, Illumina [25844936] (imputed) 51 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90018819 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic glomerulonephritis 566 European ancestry cases, 475,255 European ancestry controls, 210 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Affymetrix, Illumina [25844108] (imputed) 2 glomerulonephritis http://purl.obolibrary.org/obo/MONDO_0002462 GCST90018820 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic pancreatitis 1,424 European ancestry cases, 476,104 European ancestry controls, 457 East Asian ancestry cases, 177,471 East Asian ancestry controls NA Affymetrix, Illumina [25843262] (imputed) 4 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90018821 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic renal failure 8,287 European ancestry cases, 474,571 European ancestry controls, 2,117 East Asian ancestry cases, 174,345 East Asian ancestry controls NA Affymetrix, Illumina [25844740] (imputed) 2 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90018822 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic sinusitis 7,529 European ancestry cases, 444,966 European ancestry controls, 4,617 East Asian ancestry cases, 152,226 East Asian ancestry controls NA Affymetrix, Illumina [25838895] (imputed) 6 chronic rhinosinusitis http://www.ebi.ac.uk/efo/EFO_1000024 GCST90018823 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic bronchitis 10,159 European ancestry cases, 440,263 European ancestry controls, 271 East Asian ancestry cases, 161,803 East Asian ancestry controls NA Affymetrix, Illumina [25840074] (imputed) 4 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST90018824 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Chronic gastritis 3,645 European ancestry cases, 441,451 European ancestry controls, 744 East Asian ancestry cases, 177,982 East Asian ancestry controls NA Affymetrix, Illumina [25841562] (imputed) 0 chronic gastritis http://www.ebi.ac.uk/efo/EFO_0000337 GCST90018825 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cirrhosis 122 European ancestry cases, 347,284 European ancestry controls, 2,551 East Asian ancestry cases, 176,175 East Asian ancestry controls NA Affymetrix, Illumina [20457790] (imputed) 4 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90018826 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Colon polyp 22,049 European ancestry cases, 332,368 European ancestry controls, 4,768 East Asian ancestry cases, 166,052 East Asian ancestry controls NA Affymetrix, Illumina [20457468] (imputed) 37 polyp of colon http://purl.obolibrary.org/obo/MONDO_0021400 GCST90018827 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Compression fracture 1,796 European ancestry cases, 335,983 European ancestry controls, 2,856 East Asian ancestry cases, 175,870 East Asian ancestry controls NA Affymetrix, Illumina [20457262] (imputed) 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90018828 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Constipation 15,902 European ancestry cases, 395,721 European ancestry controls, 397 East Asian ancestry cases, 176,232 East Asian ancestry controls NA Affymetrix, Illumina [25839155] (imputed) 2 Constipation http://purl.obolibrary.org/obo/HP_0002019 GCST90018829 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Contact dermatitis 3,691 European ancestry cases, 475,075 European ancestry controls, 247 East Asian ancestry cases, 161,777 East Asian ancestry controls NA Affymetrix, Illumina [25842533] (imputed) 1 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90018830 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Cystitis 4,921 European ancestry cases, 450,694 European ancestry controls, 1,665 East Asian ancestry cases, 175,288 East Asian ancestry controls NA Affymetrix, Illumina [25842667] (imputed) 2 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90018831 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Diabetic nephropathy 1,032 European ancestry cases, 451,248 European ancestry controls, 220 East Asian ancestry cases, 132,764 East Asian ancestry controls NA Affymetrix, Illumina [25836444] (imputed) 1 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90018832 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Depression 13,559 European ancestry cases, 435,855 European ancestry controls, 836 East Asian ancestry cases, 177,794 East Asian ancestry controls NA Affymetrix, Illumina [25842841] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90018833 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Dilated cardiomyopathy 1,444 European ancestry cases, 353,937 European ancestry controls, 417 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Affymetrix, Illumina [20458130] (imputed) 0 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST90018834 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Diphtheria 12,431 European ancestry cases, 341,584 European ancestry controls, 541 East Asian ancestry cases, 170,247 East Asian ancestry controls NA Affymetrix, Illumina [20457312] (imputed) 0 diphtheria http://www.ebi.ac.uk/efo/EFO_0005549 GCST90018835 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Dysentery 2,733 European ancestry cases, 346,689 European ancestry controls, 411 East Asian ancestry cases, 178,071 East Asian ancestry controls NA Affymetrix, Illumina [20457834] (imputed) 2 dysentery http://www.ebi.ac.uk/efo/EFO_1001869 GCST90018836 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ectopic pregnancy 1,514 European ancestry cases, 250,492 European ancestry controls, 605 East Asian ancestry cases, 82,156 East Asian ancestry controls NA Affymetrix, Illumina [25786799] (imputed) 0 Ectopic pregnancy http://purl.obolibrary.org/obo/HP_0031456 GCST90018837 Genome-wide genotyping array 2022-10-19 36042491 Xiu X 2022-08-31 BMC Med www.ncbi.nlm.nih.gov/pubmed/36042491 Genetic evidence for a causal relationship between type 2 diabetes and peripheral artery disease in both Europeans and East Asians. Type 2 diabetes or peripheral artery disease (MTAG) 21,926 European ancestry type 2 diabetes cases, 5,673 European ancestry peripheral artery disease cases, 702,298 European ancestry controls NA NR [8540000] (imputed) 2 type 2 diabetes mellitus, peripheral arterial disease http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0004265 GCST90179113 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Interstitial lung disease 2,267 European ancestry cases, 467,560 European ancestry controls, 1,046 East Asian ancestry cases, 176,974 East Asian ancestry controls NA Affymetrix, Illumina [25843170] (imputed) 8 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90018863 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ischemic stroke 11,929 European ancestry cases, 472,192 European ancestry controls, 22,664 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Affymetrix, Illumina [25844498] (imputed) 15 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90018864 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Idiopathic thrombocytopenic purpura 675 European ancestry cases, 488,749 European ancestry controls, 168 East Asian ancestry cases, 178,558 East Asian ancestry controls NA Affymetrix, Illumina [25845163] (imputed) 0 autoimmune thrombocytopenic purpura http://www.ebi.ac.uk/efo/EFO_0007160 GCST90018865 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. IgA nephropathy 15,587 European ancestry cases, 462,197 European ancestry controls, 71 East Asian ancestry cases, 175,288 East Asian ancestry controls NA Affymetrix, Illumina [25844273] (imputed) 8 IGA glomerulonephritis http://www.ebi.ac.uk/efo/EFO_0004194 GCST90018866 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ileus 2,911 European ancestry cases, 395,721 European ancestry controls, 1,771 East Asian ancestry cases, 176,232 East Asian ancestry controls NA Affymetrix, Illumina [25838128] (imputed) 0 ileus http://purl.obolibrary.org/obo/MONDO_0004567 GCST90018867 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Inguinal hernia 16,725 European ancestry cases, 428,356 European ancestry controls, 1,664 East Asian ancestry cases, 177,062 East Asian ancestry controls NA Affymetrix, Illumina [25841416] (imputed) 23 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90018868 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Insomnia 1,402 European ancestry cases, 485,225 European ancestry controls, 389 East Asian ancestry cases, 177,864 East Asian ancestry controls NA Affymetrix, Illumina [25845016] (imputed) 1 insomnia measurement http://www.ebi.ac.uk/efo/EFO_0007876 GCST90018869 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Intracerebral hemorrhage 1,935 European ancestry cases, 471,578 European ancestry controls, 1,456 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Affymetrix, Illumina [25841532] (imputed) 3 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90018870 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Iritis 2,616 European ancestry cases, 478,126 European ancestry controls, 110 East Asian ancestry cases, 175,543 East Asian ancestry controls NA Affymetrix, Illumina [25844196] (imputed) 6 iritis http://www.ebi.ac.uk/efo/EFO_1000997 GCST90018871 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Iron deficiency anemia 12,317 European ancestry cases, 468,624 European ancestry controls, 4,618 East Asian ancestry cases, 174,057 East Asian ancestry controls NA Affymetrix, Illumina [25844780] (imputed) 4 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90018872 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Juvenile rheumatoid arthritis 216 European ancestry cases, 409,001 European ancestry controls, 110 East Asian ancestry cases, 173,268 East Asian ancestry controls NA Affymetrix, Illumina [25833140] (imputed) 1 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST90018873 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Keloid 668 European ancestry cases, 481,244 European ancestry controls, 1,055 East Asian ancestry cases, 177,671 East Asian ancestry controls NA Affymetrix, Illumina [25844469] (imputed) 5 Keloid http://www.ebi.ac.uk/efo/EFO_0004212 GCST90018874 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Lung cancer 3,791 European ancestry cases, 489,012 European ancestry controls, 4,444 East Asian ancestry cases, 174,282 East Asian ancestry controls NA Affymetrix, Illumina [25845450] (imputed) 11 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90018875 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Myasthenia gravis 197 European ancestry cases, 354,945 European ancestry controls, 81 East Asian ancestry cases, 178,630 East Asian ancestry controls NA Affymetrix, Illumina [20458161] (imputed) 0 Myasthenia gravis http://www.ebi.ac.uk/efo/EFO_0004991 GCST90018876 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Myocardial infarction 20,917 European ancestry cases, 440,906 European ancestry controls, 14,992 East Asian ancestry cases, 146,214 East Asian ancestry controls NA Affymetrix, Illumina [25841367] (imputed) 71 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90018877 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Malignant lymphoma 3,546 European ancestry cases, 487,257 European ancestry controls, 335 East Asian ancestry cases, 177,342 East Asian ancestry controls NA Affymetrix, Illumina [25845276] (imputed) 7 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90018878 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mastopathy 2,541 European ancestry cases, 257,308 European ancestry controls, 575 East Asian ancestry cases, 82,186 East Asian ancestry controls NA Affymetrix, Illumina [25793968] (imputed) 1 breast fibrocystic disease http://www.ebi.ac.uk/efo/EFO_0003014 GCST90018879 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Meniere's disease 1,526 European ancestry cases, 481,248 European ancestry controls, 1,290 East Asian ancestry cases, 177,436 East Asian ancestry controls NA Affymetrix, Illumina [25844443] (imputed) 3 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90018880 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Metal allergy 2,409 European ancestry cases, 350,904 European ancestry controls, 278 East Asian ancestry cases, 161,777 East Asian ancestry controls NA Affymetrix, Illumina [20456616] (imputed) 1 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90018881 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Myocarditis 633 European ancestry cases, 427,278 European ancestry controls, 102 East Asian ancestry cases, 177,745 East Asian ancestry controls NA Affymetrix, Illumina [25823913] (imputed) 0 myocarditis http://www.ebi.ac.uk/efo/EFO_0009609 GCST90018882 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Nasal polyps 5,093 European ancestry cases, 444,966 European ancestry controls, 160 East Asian ancestry cases, 151,846 East Asian ancestry controls NA Affymetrix, Illumina [25837843] (imputed) 22 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90018883 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Nephrotic syndrome 775 European ancestry cases, 475,255 European ancestry controls, 1,314 East Asian ancestry cases, 177,412 East Asian ancestry controls NA Affymetrix, Illumina [25844401] (imputed) 2 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90018884 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Neuropathic bladder 2,237 European ancestry cases, 464,793 European ancestry controls, 308 East Asian ancestry cases, 178,418 East Asian ancestry controls NA Affymetrix, Illumina [25842983] (imputed) 2 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90018885 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Non-tuberculous mycobacterial infection 26 European ancestry cases, 341,584 European ancestry controls, 64 East Asian ancestry cases, 172,320 East Asian ancestry controls NA Affymetrix, Illumina [20456798] (imputed) 0 Mycobacterium infection http://www.ebi.ac.uk/efo/EFO_0009429 GCST90018886 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Osteoporosis 8,520 European ancestry cases, 479,981 European ancestry controls, 9,794 East Asian ancestry cases, 168,932 East Asian ancestry controls NA Affymetrix, Illumina [25844994] (imputed) 21 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90018887 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Rheumatic fever 390 European ancestry cases, 476,850 European ancestry controls, 152 East Asian ancestry cases, 170,247 East Asian ancestry controls NA Affymetrix, Illumina [25843898] (imputed) 0 susceptibility to rheumatic fever measurement http://www.ebi.ac.uk/efo/EFO_0008416 GCST90018913 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ringworm 46 European ancestry cases, 354,498 European ancestry controls, 692 East Asian ancestry cases, 178,034 East Asian ancestry controls NA Affymetrix, Illumina [20458126] (imputed) 1 tinea http://www.ebi.ac.uk/efo/EFO_0007510 GCST90018914 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Stable angina pectoris 17,894 European ancestry cases, 325,132 European ancestry controls, 18,833 East Asian ancestry cases, 146,214 East Asian ancestry controls NA Affymetrix, Illumina [20456336] (imputed) 50 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90018915 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Sleep apnea syndrome 13,818 European ancestry cases, 463,035 European ancestry controls, 473 East Asian ancestry cases, 177,864 East Asian ancestry controls NA Affymetrix, Illumina [25843213] (imputed) 2 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90018916 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Systemic lupus erythematosus 647 European ancestry cases, 482,264 European ancestry controls, 317 East Asian ancestry cases, 175,937 East Asian ancestry controls NA Affymetrix, Illumina [25844568] (imputed) 4 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90018917 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Sarcoidosis 1,718 European ancestry cases, 484,955 European ancestry controls, 220 East Asian ancestry cases, 177,667 East Asian ancestry controls NA Affymetrix, Illumina [25845061] (imputed) 5 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90018918 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Schizophrenia 6,334 European ancestry cases, 445,120 European ancestry controls, 99 East Asian ancestry cases, 177,794 East Asian ancestry controls NA Affymetrix, Illumina [25843027] (imputed) 1 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90018919 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Sjögren's syndrome 1,296 European ancestry cases, 482,717 European ancestry controls, 303 East Asian ancestry cases, 175,599 East Asian ancestry controls NA Affymetrix, Illumina [25844664] (imputed) 3 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90018920 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Skin cancer 25,928 European ancestry cases, 466,275 European ancestry controls, 154 East Asian ancestry cases, 178,572 East Asian ancestry controls NA Affymetrix, Illumina [25845421] (imputed) 50 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90018921 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Spinal canal stenosis 9,660 European ancestry cases, 445,127 European ancestry controls, 661 East Asian ancestry cases, 178,065 East Asian ancestry controls NA Affymetrix, Illumina [25840105] (imputed) 11 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90018922 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Subarachnoid hemorrhage 1,693 European ancestry cases, 471,562 European ancestry controls, 1,203 East Asian ancestry cases, 152,022 East Asian ancestry controls NA Affymetrix, Illumina [25841499] (imputed) 1 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90018923 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Substance dependence 868 European ancestry cases, 482,988 European ancestry controls, 118 East Asian ancestry cases, 178,608 East Asian ancestry controls NA Affymetrix, Illumina [25844850] (imputed) 1 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST90018924 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Type 1 diabetes 6,447 European ancestry cases, 451,248 European ancestry controls, 1,219 East Asian ancestry cases, 132,032 East Asian ancestry controls NA Affymetrix, Illumina [25837106] (imputed) 14 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90018925 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Type 2 diabetes 38,841 European ancestry cases, 451,248 European ancestry controls, 45,383 East Asian ancestry cases, 132,032 East Asian ancestry controls NA Affymetrix, Illumina [25845091] (imputed) 209 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90018926 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Stevens-Johnson syndrome 312 European ancestry cases, 483,011 European ancestry controls, 93 East Asian ancestry cases, 171,753 East Asian ancestry controls NA Affymetrix, Illumina [25844251] (imputed) 2 Stevens-Johnson syndrome http://www.ebi.ac.uk/efo/EFO_0004276 GCST90018927 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Tatto pigmentation 810 European ancestry cases, 351,023 European ancestry controls, 224 East Asian ancestry cases, 178,502 East Asian ancestry controls NA Affymetrix, Illumina [20457982] (imputed) 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90018928 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Thyroid cancer 1,054 European ancestry cases, 490,920 European ancestry controls, 361 East Asian ancestry cases, 178,362 East Asian ancestry controls NA Affymetrix, Illumina [25845394] (imputed) 3 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90018929 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Tonsillitis 4,712 European ancestry cases, 454,117 European ancestry controls, 420 East Asian ancestry cases, 151,846 East Asian ancestry controls NA Affymetrix, Illumina [25839836] (imputed) 0 pharyngitis http://purl.obolibrary.org/obo/MONDO_0002258 GCST90018930 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Typhoid fever 2,733 European ancestry cases, 346,689 European ancestry controls, 257 East Asian ancestry cases, 178,071 East Asian ancestry controls NA Affymetrix, Illumina [20457818] (imputed) 1 typhoid fever http://www.ebi.ac.uk/efo/EFO_0006789 GCST90018931 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Unstable angina pectoris 9,481 European ancestry cases, 446,987 European ancestry controls, 5,891 East Asian ancestry cases, 146,214 East Asian ancestry controls NA Affymetrix, Illumina [25840389] (imputed) 22 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90018932 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ulcerative colitis 5,371 European ancestry cases, 412,561 European ancestry controls, 314 East Asian ancestry cases, 178,375 East Asian ancestry controls NA Affymetrix, Illumina [25840981] (imputed) 19 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90018933 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Uterine fibroids 21,024 European ancestry cases, 237,694 European ancestry controls, 14,475 East Asian ancestry cases, 65,733 East Asian ancestry controls NA Affymetrix, Illumina [25795146] (imputed) 53 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90018934 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Urolithiasis 6,223 European ancestry cases, 482,123 European ancestry controls, 11,699 East Asian ancestry cases, 167,027 East Asian ancestry controls NA Affymetrix, Illumina [25845211] (imputed) 35 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST90018935 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Urticaria 1,057 European ancestry cases, 482,892 European ancestry controls, 9,893 East Asian ancestry cases, 162,190 East Asian ancestry controls NA Affymetrix, Illumina [25844326] (imputed) 3 urticaria http://www.ebi.ac.uk/efo/EFO_0005531 GCST90018936 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Uterine prolapse 10,647 European ancestry cases, 224,175 European ancestry controls, 423 East Asian ancestry cases, 82,338 East Asian ancestry controls NA Affymetrix, Illumina [25752093] (imputed) 11 uterine prolapse http://www.ebi.ac.uk/efo/EFO_1001864 GCST90018937 Genome-wide genotyping array 2023-02-27 36543808 Do AR 2022-12-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36543808 A genome-wide association study implicates the pleiotropic effect of NMUR2 on asthma and COPD. Asthma or chronic obstructive pulmonary disease (pleiotropy) 1,391 Korean ancestry asthma cases, 1,091 Korean ancestry COPD cases, 5,346 Korean ancestry controls 13,475 European ancestry asthma cases, 7,822 European ancestry COPD cases, 109,871 European ancestry controls NR [4933459] (imputed) 6 asthma, chronic obstructive pulmonary disease http://purl.obolibrary.org/obo/MONDO_0004979, http://www.ebi.ac.uk/efo/EFO_0000341 GCST90255359 Genome-wide genotyping array 2023-02-27 36543808 Do AR 2022-12-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36543808 A genome-wide association study implicates the pleiotropic effect of NMUR2 on asthma and COPD. Asthma 1,391 Korean ancestry cases, 5,346 Korean ancestry controls 13,475 European ancestry cases, 109,871 European ancestry controls NR [4933459] (imputed) 4 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90255360 Genome-wide genotyping array 2023-02-27 36543808 Do AR 2022-12-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36543808 A genome-wide association study implicates the pleiotropic effect of NMUR2 on asthma and COPD. Chronic obstructive pulmonary disease 1,091 Korean ancestry cases, 5,346 Korean ancestry controls 7,822 European ancestry cases, 109,871 European ancestry controls NR [4933459] (imputed) 4 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90255361 Genome-wide genotyping array 2022-09-21 36068934 Kim SK 2022-07-01 Cartilage www.ncbi.nlm.nih.gov/pubmed/36068934 A Genome-Wide Association Study Reveals Two Genetic Markers for Chondromalacia. Chondromalacia 3,872 European ancestry cases, 518,212 European ancestry controls NA Affymetrix [9161987] (imputed) 2 chondromalacia http://purl.obolibrary.org/obo/MONDO_0002342 GCST90137415 Genome-wide genotyping array 2022-07-29 35451555 Rashkin SR 2022-04-22 Am J Med Genet A www.ncbi.nlm.nih.gov/pubmed/35451555 A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study. Obstructive heart defect 715 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Oceanian ancestry, NR ancestry case-parental trios NA Illumina [3335624] 4 congenital heart disease http://www.ebi.ac.uk/efo/EFO_0005207 GCST90131426 Genome-wide genotyping array 2022-07-29 35451555 Rashkin SR 2022-04-22 Am J Med Genet A www.ncbi.nlm.nih.gov/pubmed/35451555 A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study. Obstructive heart defect 1,137 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Oceanian ancestry, NR ancestry infant cases, 1,488 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Oceanian ancestry, NR ancestry infant controls NA Illumina [3335624] 1 congenital heart disease http://www.ebi.ac.uk/efo/EFO_0005207 GCST90131427 Genome-wide genotyping array 2022-07-29 35451555 Rashkin SR 2022-04-22 Am J Med Genet A www.ncbi.nlm.nih.gov/pubmed/35451555 A genome-wide association study of obstructive heart defects among participants in the National Birth Defects Prevention Study. Obstructive heart defect (maternal genotype effect) 1,266 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Oceanian ancestry, NR ancestry mothers of cases, 1,515 European ancestry, African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, Oceanian ancestry, NR ancestry mother of controls NA Illumina [3335624] 1 congenital heart disease, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005207, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90131428 Genome-wide genotyping array 2022-04-20 34537190 Yousaf A 2021-09-16 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34537190 Genome-wide association study identifies three susceptibility loci for trichilemmal cysts. Trichilemmal cysts 2,711 British ancestry cases, 201,078 British ancestry controls 2,620 British ancestry cases, 202,173 British ancestry controls Affymetrix [10644239] (imputed) 1 Trichilemmal cyst http://purl.obolibrary.org/obo/HP_0025246 GCST90101833 Genome-wide genotyping array 2022-04-20 34537190 Yousaf A 2021-09-16 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34537190 Genome-wide association study identifies three susceptibility loci for trichilemmal cysts. Trichilemmal cysts 5,331 British ancestry cases, 403,251 British ancestry controls NA Affymetrix [10644239] (imputed) 3 Trichilemmal cyst http://purl.obolibrary.org/obo/HP_0025246 GCST90101834 Genome-wide genotyping array 2022-04-20 34537190 Yousaf A 2021-09-16 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34537190 Genome-wide association study identifies three susceptibility loci for trichilemmal cysts. Epidermal inclusion cysts 2,806 British ancestry cases, 405,776 British ancestry controls NA Affymetrix [10644239] (imputed) 0 Epidermal Inclusion Cyst http://www.ebi.ac.uk/efo/EFO_1000243 GCST90101835 Genome-wide genotyping array 2022-10-03 34568709 Santoro N 2021-08-18 J Endocr Soc www.ncbi.nlm.nih.gov/pubmed/34568709 Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes. HDL cholesterol levels in type 2 diabetes 1,037 youth cases NA Illumina [17642824] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90044894 Genome-wide genotyping array 2022-10-03 34568709 Santoro N 2021-08-18 J Endocr Soc www.ncbi.nlm.nih.gov/pubmed/34568709 Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes. Triglyceride levels in type 2 diabetes 1,037 youth cases NA Illumina [17642824] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90044895 Genome-wide genotyping array 2022-10-03 34568709 Santoro N 2021-08-18 J Endocr Soc www.ncbi.nlm.nih.gov/pubmed/34568709 Genome-wide Association Study of Lipid Traits in Youth With Type 2 Diabetes. LDL cholesterol levels in type 2 diabetes 1,037 youth cases NA Illumina [17642824] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90158478 Genome-wide genotyping array 2023-06-08 36530128 Gibson KM 2022-12-18 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36530128 HLA-DPB1 is associated with ANCA-associated vasculitis in children. Antineutrophil cytoplasmic antibody-associated vasculitis 63 European ancestry pediatric cases, 315 European ancestry pediatric controls NA Illumina [4747947] (imputed) 4 anti-neutrophil antibody associated vasculitis http://www.ebi.ac.uk/efo/EFO_0004826 GCST90270213 Genome-wide genotyping array 2023-06-08 36530128 Gibson KM 2022-12-18 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36530128 HLA-DPB1 is associated with ANCA-associated vasculitis in children. Antineutrophil cytoplasmic antibody-associated vasculitis 56 European ancestry adult cases, 280 European ancestry adult controls NA Illumina [4747947] (imputed) 0 anti-neutrophil antibody associated vasculitis http://www.ebi.ac.uk/efo/EFO_0004826 GCST90270214 Genome-wide genotyping array 2023-06-08 36530128 Gibson KM 2022-12-18 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36530128 HLA-DPB1 is associated with ANCA-associated vasculitis in children. Antineutrophil cytoplasmic antibody-associated vasculitis 119 European ancestry cases, 595 European ancestry controls NA Illumina [4747947] (imputed) 3 anti-neutrophil antibody associated vasculitis http://www.ebi.ac.uk/efo/EFO_0004826 GCST90270215 Genome-wide genotyping array 2022-12-12 34925446 Soremekun O 2021-12-02 Front Genet www.ncbi.nlm.nih.gov/pubmed/34925446 Genome-Wide Association and Mendelian Randomization Analysis Reveal the Causal Relationship Between White Blood Cell Subtypes and Asthma in Africans. Monocyte count 16,152 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 34 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90101728 Genome-wide genotyping array 2022-12-12 34925446 Soremekun O 2021-12-02 Front Genet www.ncbi.nlm.nih.gov/pubmed/34925446 Genome-Wide Association and Mendelian Randomization Analysis Reveal the Causal Relationship Between White Blood Cell Subtypes and Asthma in Africans. Eosinophil counts 14,286 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90101729 Genome-wide genotyping array 2022-12-12 34925446 Soremekun O 2021-12-02 Front Genet www.ncbi.nlm.nih.gov/pubmed/34925446 Genome-Wide Association and Mendelian Randomization Analysis Reveal the Causal Relationship Between White Blood Cell Subtypes and Asthma in Africans. Basophil count 14,183 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90101730 Genome-wide genotyping array 2022-12-12 34925446 Soremekun O 2021-12-02 Front Genet www.ncbi.nlm.nih.gov/pubmed/34925446 Genome-Wide Association and Mendelian Randomization Analysis Reveal the Causal Relationship Between White Blood Cell Subtypes and Asthma in Africans. Neutrophil count 16,147 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 124 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90101731 Genome-wide genotyping array 2022-12-12 34925446 Soremekun O 2021-12-02 Front Genet www.ncbi.nlm.nih.gov/pubmed/34925446 Genome-Wide Association and Mendelian Randomization Analysis Reveal the Causal Relationship Between White Blood Cell Subtypes and Asthma in Africans. Lymphocyte count 16,158 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90101727 Genome-wide genotyping array 2022-12-12 34925446 Soremekun O 2021-12-02 Front Genet www.ncbi.nlm.nih.gov/pubmed/34925446 Genome-Wide Association and Mendelian Randomization Analysis Reveal the Causal Relationship Between White Blood Cell Subtypes and Asthma in Africans. White blood cell count 17,802 African ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 107 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90101726 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6386|UDP-N-acetylmuramoyl-pentapeptide biosynthesis II (lysine-containing)) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026867 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6387|UDP-N-acetylmuramoyl-pentapeptide biosynthesis I (meso-diaminopimelate containing)) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026868 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6396|superpathway of 2,3-butanediol biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 17 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026869 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6397|mycolyl-arabinogalactan-peptidoglycan complex biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 30 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026870 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6467|Kdo transfer to lipid IVA III (Chlamydia)) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026871 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6470|peptidoglycan biosynthesis V (β-lactam resistance)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026872 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6471|peptidoglycan biosynthesis IV (Enterococcus faecium)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026873 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6478|GDP-D-glycero-α-D-manno-heptose biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026874 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6507|4-deoxy-L-threo-hex-4-enopyranuronate degradation) 315 Chinese ancestry individuals NA Illumina [492582] 11 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026875 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6519|8-amino-7-oxononanoate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026876 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6545|pyrimidine deoxyribonucleotides de novo biosynthesis III) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026877 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6562|norspermidine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 35 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026878 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6588|pyruvate fermentation to acetone) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026879 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6590|superpathway of Clostridium acetobutylicum acidogenic fermentation) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026880 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6608|guanosine nucleotides degradation III) 315 Chinese ancestry individuals NA Illumina [492582] 22 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026881 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6609|adenine and adenosine salvage III) 315 Chinese ancestry individuals NA Illumina [492582] 21 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026882 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6612|superpathway of tetrahydrofolate biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026883 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6628|superpathway of L-phenylalanine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026884 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6630|superpathway of L-tyrosine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026885 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6703|preQ0 biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026887 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6708|ubiquinol-8 biosynthesis (prokaryotic)) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026888 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6737|starch degradation V) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026889 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6749|CMP-legionaminate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 24 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026890 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6876|isopropanol biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026891 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6891|thiazole biosynthesis II (Bacillus)) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026892 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6892|thiazole biosynthesis I (E. coli)) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026893 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6895|superpathway of thiamin diphosphate biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026894 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6897|thiamin salvage II) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026895 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6901|superpathway of glucose and xylose degradation) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026896 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-6969|TCA cycle V (2-oxoglutarate:ferredoxin oxidoreductase)) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026897 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7007|methyl ketone biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 30 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026898 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7013|L-1,2-propanediol degradation) 315 Chinese ancestry individuals NA Illumina [492582] 29 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026899 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7094|fatty acid salvage) 315 Chinese ancestry individuals NA Illumina [492582] 9 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026900 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7111|pyruvate fermentation to isobutanol (engineered)) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026901 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7159|chlorophyllide a biosynthesis III (aerobic, light independent)) 315 Chinese ancestry individuals NA Illumina [492582] 40 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026902 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7184|pyrimidine deoxyribonucleotides de novo biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026903 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7187|pyrimidine deoxyribonucleotides de novo biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026904 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7196|superpathway of pyrimidine ribonucleosides salvage) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026905 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7197|pyrimidine deoxyribonucleotide phosphorylation) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026906 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7199|pyrimidine deoxyribonucleosides salvage) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026907 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7200|superpathway of pyrimidine deoxyribonucleoside salvage) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026908 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7208|superpathway of pyrimidine nucleobases salvage) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026909 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7211|superpathway of pyrimidine deoxyribonucleotides de novo biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026910 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7219|adenosine ribonucleotides de novo biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026911 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7220|adenosine deoxyribonucleotides de novo biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 11 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026912 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7221|guanosine ribonucleotides de novo biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026913 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7222|guanosine deoxyribonucleotides de novo biosynthesis II) 315 Chinese ancestry individuals NA Illumina [492582] 12 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026914 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7228|superpathway of guanosine nucleotides de novo biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026915 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7229|superpathway of adenosine nucleotides de novo biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026916 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (PWY-7234|inosine-5'-phosphate biosynthesis III) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026917 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise sulcal depth 33,748 European ancestry individuals NA Affymetrix [9061022] (imputed) 854 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90095129 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise cortical surface area 33,748 European ancestry individuals NA Affymetrix [9061022] (imputed) 659 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90095130 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise cortical thickness 33,748 European ancestry individuals NA Affymetrix [9061022] (imputed) 589 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90095131 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise sulcal depth 5,199 individuals NA Affymetrix [9061022] (imputed) 15 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90095132 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise cortical surface area 5,199 individuals NA Affymetrix [9061022] (imputed) 10 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90095133 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise cortical thickness 5,199 individuals NA Affymetrix [9061022] (imputed) 4 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90095134 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise sulcal depth 8,072 individuals NA NR [13131314] (imputed) 36 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST90095135 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise cortical surface area 8,072 individuals NA NR [13131314] (imputed) 23 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90095136 Genome-wide genotyping array 2022-03-07 34910505 van der Meer D 2021-12-15 Sci Adv www.ncbi.nlm.nih.gov/pubmed/34910505 The genetic architecture of human cortical folding. Vertex-wise cortical thickness 8,072 individuals NA NR [13131314] (imputed) 8 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90095137 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (g_Anaerococcus) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026684 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (g_Dialister) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026685 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (g_Megasphaera) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026687 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (g_Prevotella) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026688 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (g_Streptococcus) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026689 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (o_Bacteroidales) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026675 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (o_Campylobacterales) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026676 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (o_Fusobacteriales) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026659 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (o_Peptostreptococcales-Tissierellales) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026677 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (p_Actinobacteriota) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026670 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (p_Proteobacteria) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026671 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Aerococcus christensenii) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026690 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Dialister micraerophilus) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026691 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Dialister propionicifaciens) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026692 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Finegoldia magna) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026693 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Gardnerella vaginalis) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026694 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Lactobacillus jensenii) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026696 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Lactobacillus mulieris) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026697 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Lactobacillus paragasseri/gasseri) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026698 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Peptoniphilus vaginalis) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026699 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Prevotella bivia) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026700 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome presence (s_Prevotella timonensis) 315 Chinese ancestry individuals NA Illumina [492582] 4 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026701 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (c_Actinobacteria) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026986 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (c_Clostridia) 315 Chinese ancestry individuals NA Illumina [492582] 11 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026987 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome relative abundance (c_Gammaproteobacteria) 315 Chinese ancestry individuals NA Illumina [492582] 24 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026665 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Fatty acids (8:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917453] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90101992 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Glycosphingolipids (d34:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917454] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90101993 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Glycosphingolipids (d38:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917455] (imputed) 20 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90101994 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Glycosphingolipids (d40:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917456] (imputed) 38 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90101995 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Glycosphingolipids (d41:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917457] (imputed) 25 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90101996 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Glycosphingolipids (d42:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917458] (imputed) 35 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90101997 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (14:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917459] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90101998 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (15:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917460] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90101999 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (16:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917461] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102000 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (16:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917462] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102001 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (17:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917463] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102002 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (18:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917464] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102003 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (18:0)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917465] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102004 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (18:0)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917466] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102005 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (18:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917467] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102006 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (18:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917468] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102007 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (18:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917469] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102008 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (20:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917470] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102009 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (20:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917471] (imputed) 1 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102010 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (20:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917472] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102011 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (20:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917473] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102012 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (20:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917474] (imputed) 2 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102013 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (20:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917475] (imputed) 3 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102014 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (22:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917476] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102015 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (22:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917477] (imputed) 2 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102016 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (35:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917503] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102042 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (35:2)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917504] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102043 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (35:2)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917505] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102044 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (35:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917506] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102045 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (35:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917507] (imputed) 3 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102046 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917508] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102047 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917509] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102048 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:3)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917510] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102049 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:3)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917511] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102050 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:3E) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917512] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102051 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:3E)1 levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917513] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102052 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:4)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917514] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102053 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:4)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917515] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102054 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:4)C levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917516] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102055 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:5)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917517] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102056 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:5)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917518] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102057 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:5)C levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917519] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102058 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:5)D levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917520] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102059 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (36:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917521] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102060 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (37:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917522] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102061 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (37:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917523] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102062 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (37:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917524] (imputed) 12 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102063 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (37:5) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917525] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102064 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (37:5E) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917526] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102065 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (37:5E)1 levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917527] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102066 Genome-wide genotyping array 2022-05-31 34813871 Liyanage U 2021-11-20 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34813871 Multi-trait genetic analysis identifies auto-immune loci associated with cutaneous melanoma. Cutaneous melanoma (MTAG) 380,287 European ancestry individuals 4,089 European ancestry cases, 11,901 European ancestry controls, 44,848 cases, 1,571,864 controls Affymetrix, Illumina [NR] (imputed) 47 cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0000389 GCST90103971 Genome-wide genotyping array 2022-05-31 34813871 Liyanage U 2021-11-20 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/34813871 Multi-trait genetic analysis identifies auto-immune loci associated with cutaneous melanoma. Melanoma 4,089 European ancestry cases, 11,901 European ancestry controls NA Illumina [NR] (imputed) 9 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90103972 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (37:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917528] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102067 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917529] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102068 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:3) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917530] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102069 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:4)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917531] (imputed) 6 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102070 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:4)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917532] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102071 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:4)C levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917533] (imputed) 5 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102072 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:5)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917534] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102073 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:5)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917535] (imputed) 4 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102074 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:6)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917536] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102075 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:6)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917537] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102076 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:6)C levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917538] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102077 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:6E) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917539] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102078 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:7) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917540] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102079 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (38:7E) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917541] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102080 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (39:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917542] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102081 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (39:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917543] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102082 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917544] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102083 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:5)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917545] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102084 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:5)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917546] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102085 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:6)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917547] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102086 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:6)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917548] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102087 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:6E) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917549] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102088 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:6E)1 levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917550] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102089 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:7)A levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917551] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102090 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (40:7)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917552] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102091 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (o-16:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917479] (imputed) 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102018 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylethanolamines (16:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917480] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90102019 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylethanolamines (18:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917481] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90102020 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylethanolamines (18:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917482] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90102021 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylethanolamines (20:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917483] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90102022 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylethanolamines (22:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917484] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90102023 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (28:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917485] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102024 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (30:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917486] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102025 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (31:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917487] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102026 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (31:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917488] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102027 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (32:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917489] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102028 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (32:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917490] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102029 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (32:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917491] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102030 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (33:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917492] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102031 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (33:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917493] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102032 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (33:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917494] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102033 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:0) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917495] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102034 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:1) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917496] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102035 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:1E) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917497] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102036 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:1E)1 levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917498] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102037 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:2) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917499] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102038 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:3)B levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917500] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102039 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:3)C levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917501] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102040 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Phosphatidylcholines (34:4) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917502] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90102041 Genome-wide genotyping array 2022-04-25 35393526 Montasser ME 2022-04-07 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35393526 An Amish founder population reveals rare-population genetic determinants of the human lipidome. Lysophosphatidylcholines (22:6) levels 650 Amish individuals 847 European American ancestry individuals Affymetrix [7917478] (imputed) 2 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90102017 Genome-wide genotyping array 2022-08-16 35626014 Pflugfelder A 2022-05-13 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/35626014 Genome-Wide Association Study Suggests the Variant rs7551288*A within the DHCR24 Gene Is Associated with Poor Overall Survival in Melanoma Patients. Survival in melanoma 556 European ancestry individuals NA Illumina [356384] 1 survival time, melanoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0000756 GCST90132200 Genome-wide genotyping array 2022-05-26 34272381 Stanzick KJ 2021-07-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34272381 Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Blood urea nitrogen levels 679,531 European ancestry individuals, 173,149 individuals NA NR [13623018] (imputed) 107 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST90103632 Genome-wide genotyping array 2022-05-26 34272381 Stanzick KJ 2021-07-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34272381 Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Estimated glomerular filtration rate (creatinine) 1,004,040 European ancestry individuals, 165,726 East Asian ancestry individuals, 13,842 African American individuals, 13,359 South Asian ancestry individuals, 4,961 Hispanic individuals, 2 individuals 417,288 European ancestry individuals NR [13633840] (imputed) 483 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90103633 Genome-wide genotyping array 2022-05-26 34272381 Stanzick KJ 2021-07-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34272381 Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Estimated glomerular filtration rate (creatinine) 1,004,040 European ancestry individuals 417,288 European ancestry individuals NR [13635145] (imputed) 178 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90103634 Genome-wide genotyping array 2022-05-26 34272381 Stanzick KJ 2021-07-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/34272381 Discovery and prioritization of variants and genes for kidney function in >1.2 million individuals. Estimated glomerular filtration rate (cystatin c) 460,826 European or unknown ancestry individuals NA NR [13621211] (imputed) 159 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90103635 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome alpha diversity (Faith phylogenetic diversity) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026703 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome alpha diversity (Pielou Evenness) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026704 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome alpha diversity (Shannon Index) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026702 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome beta diversity (Bray-curtis Dissimilarity) 315 Chinese ancestry individuals NA Illumina [492582] 10 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026667 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome beta diversity (Unweighted Unifrac) 315 Chinese ancestry individuals NA Illumina [492582] 16 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026668 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome beta diversity (Weighted Unifrac) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026669 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome dominance (g_Lactobacillus) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026686 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome dominance (s_Lactobacillus iners) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026695 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (1CMET2-PWY|N10-formyl-tetrahydrofolate biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026705 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ALL-CHORISMATE-PWY|superpathway of chorismate metabolism) 315 Chinese ancestry individuals NA Illumina [492582] 29 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026706 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ANAEROFRUCAT-PWY|homolactic fermentation) 315 Chinese ancestry individuals NA Illumina [492582] 8 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026707 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ANAGLYCOLYSIS-PWY|glycolysis III (from glucose)) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026708 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ARG+POLYAMINE-SYN|superpathway of arginine and polyamine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026709 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ARGORNPROST-PWY|arginine, ornithine and proline interconversion) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026710 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ARGSYN-PWY|L-arginine biosynthesis I (via L-ornithine)) 315 Chinese ancestry individuals NA Illumina [492582] 1 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026711 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ARO-PWY|chorismate biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026712 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (ASPASN-PWY|superpathway of L-aspartate and L-asparagine biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 5 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026713 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (BIOTIN-BIOSYNTHESIS-PWY|biotin biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026714 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (BRANCHED-CHAIN-AA-SYN-PWY|superpathway of branched amino acid biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026715 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (CALVIN-PWY|Calvin-Benson-Bassham cycle) 315 Chinese ancestry individuals NA Illumina [492582] 3 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026716 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (CATECHOL-ORTHO-CLEAVAGE-PWY|catechol degradation to β-ketoadipate) 315 Chinese ancestry individuals NA Illumina [492582] 48 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026717 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (CENTFERM-PWY|pyruvate fermentation to butanoate) 315 Chinese ancestry individuals NA Illumina [492582] 6 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026718 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (COA-PWY|coenzyme A biosynthesis I) 315 Chinese ancestry individuals NA Illumina [492582] 2 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026719 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (CODH-PWY|reductive acetyl coenzyme A pathway) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026720 Genome-wide genotyping array 2022-09-28 34282934 Fan W 2021-07-20 mSystems www.ncbi.nlm.nih.gov/pubmed/34282934 Association between Human Genetic Variants and the Vaginal Bacteriome of Pregnant Women. Vaginal microbiome MetaCyc pathway (COLANSYN-PWY|colanic acid building blocks biosynthesis) 315 Chinese ancestry individuals NA Illumina [492582] 7 vaginal microbiome measurement http://www.ebi.ac.uk/efo/EFO_0011013 GCST90026721 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive performance (attention) (longitudinal) 402 European ancestry individuals NA Illumina [7464105] (imputed) 25 attention function measurement http://www.ebi.ac.uk/efo/EFO_0007636 GCST90104685 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive performance (attention) 806 European ancestry individuals NA Illumina [7464105] (imputed) 17 attention function measurement http://www.ebi.ac.uk/efo/EFO_0007636 GCST90104686 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Executive function 686 European ancestry individuals NA Illumina [7464105] (imputed) 17 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90104687 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Executive function (longitudinal) 234 European ancestry individuals NA Illumina [7464105] (imputed) 35 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90104688 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive performance (visuoconstruction) 429 European ancestry individuals NA Illumina [7464105] (imputed) 29 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90104689 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive performance (visuoconstruction) (longitudinal) 149 European ancestry individuals NA Illumina [7464105] (imputed) 34 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90104690 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive performance (language ability) 849 European ancestry individuals NA Illumina [7464105] (imputed) 20 language measurement http://www.ebi.ac.uk/efo/EFO_0007797 GCST90104691 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive performance (language ability) (longitudinal) 409 European ancestry individuals NA Illumina [7464105] (imputed) 33 language measurement http://www.ebi.ac.uk/efo/EFO_0007797 GCST90104692 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive function (delayed memory) (longitudinal) 337 European ancestry individuals NA Illumina [7464105] (imputed) 20 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90104693 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive function (delayed memory) 729 European ancestry individuals NA Illumina [7464105] (imputed) 27 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90104694 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive function (immediate memory) 797 European ancestry individuals NA Illumina [7464105] (imputed) 20 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90104695 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cognitive function (immediate memory) (longitudinal) 345 European ancestry individuals NA Illumina [7464105] (imputed) 49 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90104696 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Global cognition (Mini Mental State Examination) 867 European ancestry individuals NA Illumina [7464105] (imputed) 49 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90104697 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Global cognition (Mini Mental State Examination) (longitudinal) 520 European ancestry individuals NA Illumina [7464105] (imputed) 42 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90104698 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Right hippocampal volume 605 European ancestry individuals NA Illumina [7464105] (imputed) 20 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90104699 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Hippocampal volume 605 European ancestry individuals NA Illumina [7464105] (imputed) 17 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90104700 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Left hippocampal volume 605 European ancestry individuals NA Illumina [7464105] (imputed) 17 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90104701 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. White matter lesions (Fazekas score) 606 European ancestry individuals NA Illumina [7464105] (imputed) 33 white matter lesion progression measurement http://www.ebi.ac.uk/efo/EFO_0007746 GCST90104707 Genome-wide genotyping array 2022-06-20 35386118 Homann J 2022-03-21 Front Aging Neurosci www.ncbi.nlm.nih.gov/pubmed/35386118 Genome-Wide Association Study of Alzheimer's Disease Brain Imaging Biomarkers and Neuropsychological Phenotypes in the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery Dataset. Cortical thickness 560 European ancestry individuals NA Illumina [7464105] (imputed) 34 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90104703 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Piperine levels 2,466 Black/admixed ancestry individuals NA Illumina [153810] 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90176330 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pravastatin levels 2,466 Black/admixed ancestry individuals NA Illumina [150053] 0 pravastatin measurement http://www.ebi.ac.uk/efo/EFO_0801215 GCST90176126 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pro-gly levels 2,466 Black/admixed ancestry individuals NA Illumina [152972] 0 pro-gly measurement http://www.ebi.ac.uk/efo/EFO_0801216 GCST90176331 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Proline levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157711] 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90176332 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Proline betaine levels 2,466 Black/admixed ancestry individuals NA Illumina [155700] 0 proline betaine measurement http://www.ebi.ac.uk/efo/EFO_0011000 GCST90176333 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pseudouridine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152624] 1 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90176070 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pseudouridine levels 2,466 Black/admixed ancestry individuals NA Illumina [153349] 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90176334 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pyroglutamic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [193105] 1 L-Pyroglutamic acid measurement http://www.ebi.ac.uk/efo/EFO_0021628 GCST90176071 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pyruvic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [164147] 0 pyruvic acid measurement http://www.ebi.ac.uk/efo/EFO_0801217 GCST90176072 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10) 2,466 Black/admixed ancestry individuals NA Illumina [156571] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176335 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10006) 2,466 Black/admixed ancestry individuals NA Illumina [150907] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176336 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1001) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153780] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176337 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10010) 2,466 Black/admixed ancestry individuals NA Illumina [152305] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176338 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10015) 2,466 Black/admixed ancestry individuals NA Illumina [158425] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176339 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10023) 2,466 Black/admixed ancestry individuals NA Illumina [155053] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176340 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1004) 2,466 Black/admixed ancestry individuals NA Illumina [152574] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176341 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10049) 2,466 Black/admixed ancestry individuals NA Illumina [149977] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176342 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1005) 2,466 Black/admixed ancestry individuals NA Illumina [151549] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176343 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10050) 2,466 Black/admixed ancestry individuals NA Illumina [151675] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176344 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10052) 2,466 Black/admixed ancestry individuals NA Illumina [155342] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176345 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10052) 2,466 Black/admixed ancestry individuals NA Illumina [150677] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178717 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10054) 2,466 Black/admixed ancestry individuals NA Illumina [157403] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176346 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10057) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153696] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176347 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10058) 2,466 Black/admixed ancestry individuals NA Illumina [154452] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176348 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10060) 2,466 Black/admixed ancestry individuals NA Illumina [160248] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176349 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1071) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151783] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176442 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10710) 2,466 Black/admixed ancestry individuals NA Illumina [168213] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176443 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10710) 2,466 Black/admixed ancestry individuals NA Illumina [151294] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178949 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10719) 2,466 Black/admixed ancestry individuals NA Illumina [148643] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176444 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10724) 2,466 Black/admixed ancestry individuals NA Illumina [160373] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176445 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10729) 2,466 Black/admixed ancestry individuals NA Illumina [152113] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176446 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10754) 2,466 Black/admixed ancestry individuals NA Illumina [174911] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178950 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10761) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153351] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176447 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10763) 2,466 Black/admixed ancestry individuals NA Illumina [152340] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176448 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10769) 2,466 Black/admixed ancestry individuals NA Illumina [136277] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176449 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10773) 2,466 Black/admixed ancestry individuals NA Illumina [155799] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176450 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10833) 2,466 Black/admixed ancestry individuals NA Illumina [162141] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176451 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10833) 2,466 Black/admixed ancestry individuals NA Illumina [160358] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178951 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10834) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158254] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176452 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10839) 2,466 Black/admixed ancestry individuals NA Illumina [161560] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176453 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10852) 2,466 Black/admixed ancestry individuals NA Illumina [158800] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176454 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10852) 2,466 Black/admixed ancestry individuals NA Illumina [152283] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178952 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10855) 2,466 Black/admixed ancestry individuals NA Illumina [162158] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176455 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10869) 2,466 Black/admixed ancestry individuals NA Illumina [147899] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176456 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1087) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154597] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176457 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10874) 2,466 Black/admixed ancestry individuals NA Illumina [153940] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176458 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10889) 2,466 Black/admixed ancestry individuals NA Illumina [157430] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176459 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1093) 2,466 Black/admixed ancestry individuals NA Illumina [154428] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176460 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1093) 2,466 Black/admixed ancestry individuals NA Illumina [152980] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178727 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1094) 2,466 Black/admixed ancestry individuals NA Illumina [176954] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178953 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10584) 2,466 Black/admixed ancestry individuals NA Illumina [152472] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176426 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10591) 2,466 Black/admixed ancestry individuals NA Illumina [160641] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176427 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10591) 2,466 Black/admixed ancestry individuals NA Illumina [165663] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178724 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10598) 2,466 Black/admixed ancestry individuals NA Illumina [153623] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178943 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10601) 2,466 Black/admixed ancestry individuals NA Illumina [141274] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176428 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10607) 2,466 Black/admixed ancestry individuals NA Illumina [169511] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176429 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10609) 2,466 Black/admixed ancestry individuals NA Illumina [138417] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176430 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10618) 2,466 Black/admixed ancestry individuals NA Illumina [171097] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176431 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10623) 2,466 Black/admixed ancestry individuals NA Illumina [158736] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176432 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10623) 2,466 Black/admixed ancestry individuals NA Illumina [148944] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178725 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10627) 2,466 Black/admixed ancestry individuals NA Illumina [148456] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176433 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10627) 2,466 Black/admixed ancestry individuals NA Illumina [161048] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178944 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10629) 2,466 Black/admixed ancestry individuals NA Illumina [156269] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176434 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10629) 2,466 Black/admixed ancestry individuals NA Illumina [150199] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178726 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1063) 2,466 Black/admixed ancestry individuals NA Illumina [156198] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176435 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10664) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155183] 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176436 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10673) 2,466 Black/admixed ancestry individuals NA Illumina [160822] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176437 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10673) 2,466 Black/admixed ancestry individuals NA Illumina [159243] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178945 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10677) 2,466 Black/admixed ancestry individuals NA Illumina [154346] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176438 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10677) 2,466 Black/admixed ancestry individuals NA Illumina [159866] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178946 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10682) 2,466 Black/admixed ancestry individuals NA Illumina [151421] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176439 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10682) 2,466 Black/admixed ancestry individuals NA Illumina [137221] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178947 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10685) 2,466 Black/admixed ancestry individuals NA Illumina [153159] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178948 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1070) 2,466 Black/admixed ancestry individuals NA Illumina [151332] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176440 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10705) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156240] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176441 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10274) 2,466 Black/admixed ancestry individuals NA Illumina [151739] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176393 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10277) 2,466 Black/admixed ancestry individuals NA Illumina [158437] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176394 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10277) 2,466 Black/admixed ancestry individuals NA Illumina [145564] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178928 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10291) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149667] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176395 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10293) 2,466 Black/admixed ancestry individuals NA Illumina [165335] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176396 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10293) 2,466 Black/admixed ancestry individuals NA Illumina [143757] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178929 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10305) 2,466 Black/admixed ancestry individuals NA Illumina [150645] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176397 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10309) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160725] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176398 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10313) 2,466 Black/admixed ancestry individuals NA Illumina [152210] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176399 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10313) 2,466 Black/admixed ancestry individuals NA Illumina [146743] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178930 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10325) 2,466 Black/admixed ancestry individuals NA Illumina [150662] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176400 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10330) 2,466 Black/admixed ancestry individuals NA Illumina [150344] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176401 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10333) 2,466 Black/admixed ancestry individuals NA Illumina [163851] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176402 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10333) 2,466 Black/admixed ancestry individuals NA Illumina [144016] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178931 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10336) 2,466 Black/admixed ancestry individuals NA Illumina [159455] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178932 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10337) 2,466 Black/admixed ancestry individuals NA Illumina [152612] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176403 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10342) 2,466 Black/admixed ancestry individuals NA Illumina [159358] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176404 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10342) 2,466 Black/admixed ancestry individuals NA Illumina [164681] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178933 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10352) 2,466 Black/admixed ancestry individuals NA Illumina [147602] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178934 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10356) 2,466 Black/admixed ancestry individuals NA Illumina [159968] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176405 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10356) 2,466 Black/admixed ancestry individuals NA Illumina [145773] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178935 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10359) 2,466 Black/admixed ancestry individuals NA Illumina [153189] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176406 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1037) 2,466 Black/admixed ancestry individuals NA Illumina [152982] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176407 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10390) 2,466 Black/admixed ancestry individuals NA Illumina [202040] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178936 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10401) 2,466 Black/admixed ancestry individuals NA Illumina [162438] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176408 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10401) 2,466 Black/admixed ancestry individuals NA Illumina [207796] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178937 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10408) 2,466 Black/admixed ancestry individuals NA Illumina [151258] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176409 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10409) 2,466 Black/admixed ancestry individuals NA Illumina [161454] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176410 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10409) 2,466 Black/admixed ancestry individuals NA Illumina [174062] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178722 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10425) 2,466 Black/admixed ancestry individuals NA Illumina [158096] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176411 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10430) 2,466 Black/admixed ancestry individuals NA Illumina [148546] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176412 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10440) 2,466 Black/admixed ancestry individuals NA Illumina [150475] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176413 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10443) 2,466 Black/admixed ancestry individuals NA Illumina [154944] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176414 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10443) 2,466 Black/admixed ancestry individuals NA Illumina [142618] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178938 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10448) 2,466 Black/admixed ancestry individuals NA Illumina [154712] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176415 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10481) 2,466 Black/admixed ancestry individuals NA Illumina [158405] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176416 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10481) 2,466 Black/admixed ancestry individuals NA Illumina [150838] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178939 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10487) 2,466 Black/admixed ancestry individuals NA Illumina [159461] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176417 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10488) 2,466 Black/admixed ancestry individuals NA Illumina [168520] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176418 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10488) 2,466 Black/admixed ancestry individuals NA Illumina [162656] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178940 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10502) 2,466 Black/admixed ancestry individuals NA Illumina [236988] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178941 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10523) 2,466 Black/admixed ancestry individuals NA Illumina [157175] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176419 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10523) 2,466 Black/admixed ancestry individuals NA Illumina [150462] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178723 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10524) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160414] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176420 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10536) 2,466 Black/admixed ancestry individuals NA Illumina [166208] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176421 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10537) 2,466 Black/admixed ancestry individuals NA Illumina [166055] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178942 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10546) 2,466 Black/admixed ancestry individuals NA Illumina [161380] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176422 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1056) 2,466 Black/admixed ancestry individuals NA Illumina [152491] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176423 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10574) 2,466 Black/admixed ancestry individuals NA Illumina [152303] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176424 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10575) 2,466 Black/admixed ancestry individuals NA Illumina [156081] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176425 Genome-wide sequencing 2023-11-10 37673066 Chen WC 2023-08-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37673066 Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations. Esophageal squamous cell carcinoma 1,686 Sub-Saharan African ancestry cases, 3,217 Sub-Saharan African ancestry controls NA Illumina [13256833] (imputed) 31 esophageal squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0005922 GCST90271955 Genome-wide genotyping array 2023-11-10 37673066 Chen WC 2023-08-29 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37673066 Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations. Esophageal squamous cell carcinoma 1,686 Sub-Saharan African ancestry cases, 3,217 Sub-Saharan African ancestry controls, 2,013 East Asian ancestry cases, 2,701 East Asian ancestry controls NA Illumina [4850895] (imputed) 4 esophageal squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0005922 GCST90271956 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Diacylglycerol (18:1_18:3) levels 6,572 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Diacylglycerol (18:1_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045172 GCST90277263 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_0:0) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (16:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045066 GCST90277264 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:0_0:0) levels 7,173 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (18:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045088 GCST90277265 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:1_0:0) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (18:1_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045098 GCST90277266 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (18:2_0:0) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (18:2_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045105 GCST90277267 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (20:4_0:0) levels 6,235 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (20:4_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045110 GCST90277268 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (18:0_0:0) levels 6,258 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylethanolamine (18:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045138 GCST90277269 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (18:1_0:0) levels 5,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylethanolamine (18:1_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045141 GCST90277270 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylethanolamine (18:2_0:0) levels 6,905 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylethanolamine (18:2_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045143 GCST90277271 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (14:0_16:0) levels 5,497 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (14:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045061 GCST90277272 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (14:0_18:1) levels 7,064 Finnish ancestry individuals NA Illumina [11318730] (imputed) 4 level of Phosphatidylcholine (14:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045062 GCST90277273 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (14:0_18:2) levels 6,866 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylcholine (14:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045063 GCST90277274 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (15:0_18:1) levels 6,468 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of Phosphatidylcholine (15:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045064 GCST90277275 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (15:0_18:2) levels 6,639 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Phosphatidylcholine (15:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045065 GCST90277276 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_16:0) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylcholine (16:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045067 GCST90277277 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_16:1) levels 7,172 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (16:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045068 GCST90277278 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_17:1) levels 7,076 Finnish ancestry individuals NA Illumina [11318730] (imputed) 0 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90277279 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_18:0) levels 7,154 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (16:0_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045069 GCST90277280 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_18:1) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045070 GCST90277281 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_18:2) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 6 level of Phosphatidylcholine (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045071 GCST90277282 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_18:3) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 3 level of Phosphatidylcholine (16:0_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045072 GCST90277283 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_20:1) levels 6,882 Finnish ancestry individuals NA Illumina [11318730] (imputed) 1 level of Phosphatidylcholine (16:0_20:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045073 GCST90277284 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_20:2) levels 7,135 Finnish ancestry individuals NA Illumina [11318730] (imputed) 5 level of Phosphatidylcholine (16:0_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045074 GCST90277285 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_20:3) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (16:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045075 GCST90277286 Genome-wide genotyping array 2023-11-15 37907536 Ottensmann L 2023-10-31 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37907536 Genome-wide association analysis of plasma lipidome identifies 495 genetic associations. Phosphatidylcholine (16:0_20:4) levels 7,174 Finnish ancestry individuals NA Illumina [11318730] (imputed) 2 level of Phosphatidylcholine (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045076 GCST90277287 Genome-wide genotyping array 2022-10-12 35918310 Sonehara K 2022-08-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35918310 A common deletion at BAK1 reduces enhancer activity and confers risk of intracranial germ cell tumors. Intracranial germ cell tumors 138 Japanese ancestry cases, 808 Japanese ancestry controls NA Illumina [NR] (imputed) 1 intracranial germ cell tumor http://www.ebi.ac.uk/efo/EFO_0800001 GCST90134667 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Palmitoylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90129034 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Stearoylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90129035 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-oleoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-oleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021096 GCST90129036 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-arachidonoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-arachidonoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021076 GCST90128856 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Arachidonate (20:4n6) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90128870 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Asparagine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90128871 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Aspartylphenylalanine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 aspartylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021127 GCST90128872 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Bilirubin (E,E) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90128873 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Bilirubin (E,Z or Z,E) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90128874 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Bilirubin (z,z) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90128875 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Biliverdin levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90128876 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Butyrylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 butyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020010 GCST90128877 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Carnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90128878 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Decanoylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90128879 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Acetylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90128880 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Propionylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90128881 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Isovalerylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 isovalerylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020019 GCST90128882 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hexanoylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90128883 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Octanoylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90128884 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Nonanoylcarnitine (C9) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-13431--nonanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021349 GCST90128885 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Epiandrosterone sulfate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90128886 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Gamma-glutamylglutamine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90128887 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glutamine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90128888 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glycine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90128889 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glycochenodeoxycholate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90128890 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glucose levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90128891 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hexadecanedioate (C16) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90128892 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Histidine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90128893 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Inosine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90128894 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. High density lipoprotein cholesterol levels (UKB data field 30760) (CNV mirror model) 290,940 white British ancestry individuals NA NR [28257] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90027299 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Pulse rate automated reading (UKB data field 102) (CNV mirror model) 313,183 white British ancestry individuals NA NR [28257] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90027300 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Standing height (UKB data field 50) (CNV mirror model) 330,837 white British ancestry individuals NA NR [28257] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90027301 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Apolipoprotein A levels (UKB data field 30630) (CNV mirror model) 289,352 white British ancestry individuals NA NR [28257] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90027277 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Direct low density lipoprotein levels (UKB data field 30780) (CNV mirror model) 316,377 white British ancestry individuals NA NR [28257] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90027303 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Lipoprotein A levels (UKB data field 30790) (CNV mirror model) 252,704 white British ancestry individuals NA NR [28257] 0 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90027304 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Birth weight (UKB data field 20022) (CNV mirror model) 192,408 white British ancestry individuals NA NR [28257] 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90027281 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Heel bone mineral density (UKB data field 3148) (CNV mirror model) 191,028 white British ancestry individuals NA NR [28257] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90027282 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Mean corpuscular haemoglobin (UKB data field 30050) (CNV mirror model) 322,496 white British ancestry individuals NA NR [28257] 0 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90027306 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Basal metabolic rate (UKB data field 23105) (CNV mirror model) 325,954 white British ancestry individuals NA NR [28257] 0 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST90027284 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Whole body fat mass (UKB data field 23100) (CNV mirror model) 325,438 white British ancestry individuals NA NR [28257] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90027285 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Neutrophill count (UKB data field 30140) (CNV mirror model) 321,953 white British ancestry individuals NA NR [28257] 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90027309 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Creatinine levels (UKB data field 30700) (CNV mirror model) 316,786 white British ancestry individuals NA NR [28257] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90027288 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Platelet count (UKB data field 30080) (CNV mirror model) 322,499 white British ancestry individuals NA NR [28257] 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90027311 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Red blood cell erythrocyte count (UKB data field 30010) (CNV mirror model) 322,500 white British ancestry individuals NA NR [28257] 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90027312 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Reticulocyte count (UKB data field 30250) (CNV mirror model) 317,487 white British ancestry individuals NA NR [28257] 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90027313 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Fluid intelligence score (UKB data field 20016) (CNV mirror model) 124,129 white British ancestry individuals NA NR [28257] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST90027293 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Systolic blood pressure automated reading (UKB data field 4080) (CNV mirror model) 313,181 white British ancestry individuals NA NR [28257] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90027315 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Testosterone levels (UKB data field 30850) (CNV mirror model) 287,926 white British ancestry individuals NA NR [28257] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027316 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Glucose levels (UKB data field 30740) (CNV mirror model) 290,770 white British ancestry individuals NA NR [28257] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90027296 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Hand grip strength (UKB data field 46/47) (CNV mirror model) 329,630 white British ancestry individuals NA NR [28257] 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90027297 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Glycated haemoglobin HbA1c levels (UKB data field 30750) (CNV mirror model) 316,928 white British ancestry individuals NA NR [28257] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90027298 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Urate levels (UKB data field 30880) (CNV mirror model) 316,545 white British ancestry individuals NA NR [28257] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90027319 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Urea levels (UKB data field 30670) (CNV mirror model) 316,737 white British ancestry individuals NA NR [28257] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90027320 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Vitamin D levels (UKB data field 30890) (CNV mirror model) 303,212 white British ancestry individuals NA NR [28257] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90027321 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. White blood cell leukocyte count (UKB data field 30000) (CNV mirror model) 322,497 white British ancestry individuals NA NR [28257] 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90027322 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Weight (UKB data field 21002) (CNV mirror model) 330,607 white British ancestry individuals NA NR [28257] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90027323 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Whole body fat mass (UKB data field 23100) (CNV deletion-only model) 325,438 white British ancestry individuals NA NR [9936] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90027399 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Calcium levels (UKB data field 30680) (CNV deletion-only model) 290,951 white British ancestry individuals NA NR [9936] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90027400 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Cholesterol levels (UKB data field 30690) (CNV deletion-only model) 316,939 white British ancestry individuals NA NR [9936] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90027401 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Creatinine levels (UKB data field 30700) (CNV deletion-only model) 316,786 white British ancestry individuals NA NR [9936] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90027402 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. C reactive protein levels (UKB data field 30710) (CNV deletion-only model) 316,278 white British ancestry individuals NA NR [9936] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90027403 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Cystatin C levels (UKB data field 30720) (CNV deletion-only model) 316,915 white British ancestry individuals NA NR [9936] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90027404 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Diastolic blood pressure automated reading (UKB data field 4079) (CNV deletion-only model) 313,183 white British ancestry individuals NA NR [9936] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90027405 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Eosinophill count (UKB data field 30150) (CNV deletion-only model) 321,953 white British ancestry individuals NA NR [9936] 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90027406 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Fluid intelligence score (UKB data field 20016) (CNV deletion-only model) 124,129 white British ancestry individuals NA NR [9936] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST90027407 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Forced vital capacity FVC (UKB data field 3062) (CNV deletion-only model) 304,605 white British ancestry individuals NA NR [9936] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90027408 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Gamma glutamyltransferase levels (UKB data field 30730) (CNV deletion-only model) 316,781 white British ancestry individuals NA NR [9936] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90027409 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Glucose levels (UKB data field 30740) (CNV deletion-only model) 290,770 white British ancestry individuals NA NR [9936] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90027410 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Hand grip strength (UKB data field 46/47) (CNV deletion-only model) 329,630 white British ancestry individuals NA NR [9936] 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90027411 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Glycated haemoglobin HbA1c levels (UKB data field 30750) (CNV deletion-only model) 316,928 white British ancestry individuals NA NR [9936] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90027412 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. High density lipoprotein cholesterol levels (UKB data field 30760) (CNV deletion-only model) 290,940 white British ancestry individuals NA NR [9936] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90027413 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Pulse rate automated reading (UKB data field 102) (CNV deletion-only model) 313,183 white British ancestry individuals NA NR [9936] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90027414 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Standing height (UKB data field 50) (CNV deletion-only model) 330,837 white British ancestry individuals NA NR [9936] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90027415 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. IGF 1 (UKB data field 30770) (CNV deletion-only model) 315,299 white British ancestry individuals NA NR [9936] 0 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST90027416 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Direct low density lipoprotein levels (UKB data field 30780) (CNV deletion-only model) 316,377 white British ancestry individuals NA NR [9936] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90027417 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Lipoprotein A levels (UKB data field 30790) (CNV deletion-only model) 252,704 white British ancestry individuals NA NR [9936] 0 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90027418 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Lymphocyte count (UKB data field 30120) (CNV deletion-only model) 321,953 white British ancestry individuals NA NR [9936] 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90027419 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Mean corpuscular haemoglobin (UKB data field 30050) (CNV deletion-only model) 322,496 white British ancestry individuals NA NR [9936] 0 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90027420 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Monocyte count (UKB data field 30130) (CNV deletion-only model) 321,953 white British ancestry individuals NA NR [9936] 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90027421 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Neuroticism (UKB data field 20127) (CNV deletion-only model) 269,539 white British ancestry individuals NA NR [9936] 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027422 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Neutrophill count (UKB data field 30140) (CNV deletion-only model) 321,953 white British ancestry individuals NA NR [9936] 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90027423 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Eosinophill count (UKB data field 30150) (CNV duplication-only model) 321,953 white British ancestry individuals NA NR [14070] 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90027349 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Fluid intelligence score (UKB data field 20016) (CNV duplication-only model) 124,129 white British ancestry individuals NA NR [14070] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST90027350 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Forced vital capacity FVC (UKB data field 3062) (CNV duplication-only model) 304,605 white British ancestry individuals NA NR [14070] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90027351 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Gamma glutamyltransferase levels (UKB data field 30730) (CNV duplication-only model) 316,781 white British ancestry individuals NA NR [14070] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90027352 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Glucose levels (UKB data field 30740) (CNV duplication-only model) 290,770 white British ancestry individuals NA NR [14070] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90027353 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Hand grip strength (UKB data field 46/47) (CNV duplication-only model) 329,630 white British ancestry individuals NA NR [14070] 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90027354 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Glycated haemoglobin HbA1c levels (UKB data field 30750) (CNV duplication-only model) 316,928 white British ancestry individuals NA NR [14070] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90027355 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Relative age of first facial hair (UKB data field 2375) (CNV mirror model) 148,371 white British ancestry males NA NR [28257] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90027327 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Pulse rate automated reading (UKB data field 102) (CNV duplication-only model) 313,183 white British ancestry individuals NA NR [14070] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90027357 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Standing height (UKB data field 50) (CNV duplication-only model) 330,837 white British ancestry individuals NA NR [14070] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90027358 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. IGF 1 (UKB data field 30770) (CNV duplication-only model) 315,299 white British ancestry individuals NA NR [14070] 0 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST90027359 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Direct low density lipoprotein levels (UKB data field 30780) (CNV duplication-only model) 316,377 white British ancestry individuals NA NR [14070] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90027360 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Lipoprotein A levels (UKB data field 30790) (CNV duplication-only model) 252,704 white British ancestry individuals NA NR [14070] 0 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90027361 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Lymphocyte count (UKB data field 30120) (CNV duplication-only model) 321,953 white British ancestry individuals NA NR [14070] 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90027362 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Alkaline phosphatase levels (UKB data field 30610) (CNV duplication-only model) 316,951 white British ancestry individuals NA NR [14070] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90027332 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Alanine aminotransferase levels (UKB data field 30620) (CNV duplication-only model) 316,815 white British ancestry individuals NA NR [14070] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90027333 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Apolipoprotein A levels (UKB data field 30630) (CNV duplication-only model) 289,352 white British ancestry individuals NA NR [14070] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90027334 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Apolipoprotein B levels (UKB data field 30640) (CNV duplication-only model) 315,444 white British ancestry individuals NA NR [14070] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90027335 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Sex hormone binding globulin levels (UKB data field 30830) (CNV duplication-only model) 288,310 white British ancestry individuals NA NR [14070] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90027371 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Systolic blood pressure automated reading (UKB data field 4080) (CNV duplication-only model) 313,181 white British ancestry individuals NA NR [14070] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90027372 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Testosterone levels (UKB data field 30850) (CNV duplication-only model) 287,926 white British ancestry individuals NA NR [14070] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027373 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Albumin levels (UKB data field 30600) (CNV mirror model) 291,060 white British ancestry individuals NA NR [28257] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90027274 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Alkaline phosphatase levels (UKB data field 30610) (CNV mirror model) 316,951 white British ancestry individuals NA NR [28257] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90027275 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Alanine aminotransferase levels (UKB data field 30620) (CNV mirror model) 316,815 white British ancestry individuals NA NR [28257] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90027276 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. IGF 1 (UKB data field 30770) (CNV mirror model) 315,299 white British ancestry individuals NA NR [28257] 0 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST90027302 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Apolipoprotein B levels (UKB data field 30640) (CNV mirror model) 315,444 white British ancestry individuals NA NR [28257] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90027278 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Aspartate aminotransferase levels (UKB data field 30650) (CNV mirror model) 315,807 white British ancestry individuals NA NR [28257] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90027279 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Total bilirubin levels (UKB data field 30840) (CNV mirror model) 315,664 white British ancestry individuals NA NR [28257] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90027280 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Lymphocyte count (UKB data field 30120) (CNV mirror model) 321,953 white British ancestry individuals NA NR [28257] 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90027305 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Body mass index (UKB data field 21001) (CNV mirror model) 330,497 white British ancestry individuals NA NR [28257] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90027283 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Monocyte count (UKB data field 30130) (CNV mirror model) 321,953 white British ancestry individuals NA NR [28257] 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90027307 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Neuroticism (UKB data field 20127) (CNV mirror model) 269,539 white British ancestry individuals NA NR [28257] 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027308 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Calcium levels (UKB data field 30680) (CNV mirror model) 290,951 white British ancestry individuals NA NR [28257] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90027286 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Cholesterol levels (UKB data field 30690) (CNV mirror model) 316,939 white British ancestry individuals NA NR [28257] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90027287 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Phosphate levels (UKB data field 30810) (CNV mirror model) 290,512 white British ancestry individuals NA NR [28257] 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90027310 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. C reactive protein levels (UKB data field 30710) (CNV mirror model) 316,278 white British ancestry individuals NA NR [28257] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90027289 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Cystatin C levels (UKB data field 30720) (CNV mirror model) 316,915 white British ancestry individuals NA NR [28257] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90027290 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Diastolic blood pressure automated reading (UKB data field 4079) (CNV mirror model) 313,183 white British ancestry individuals NA NR [28257] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90027291 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Eosinophill count (UKB data field 30150) (CNV mirror model) 321,953 white British ancestry individuals NA NR [28257] 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90027292 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Sex hormone binding globulin levels (UKB data field 30830) (CNV mirror model) 288,310 white British ancestry individuals NA NR [28257] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90027314 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Forced vital capacity FVC (UKB data field 3062) (CNV mirror model) 304,605 white British ancestry individuals NA NR [28257] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90027294 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Gamma glutamyltransferase levels (UKB data field 30730) (CNV mirror model) 316,781 white British ancestry individuals NA NR [28257] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90027295 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Triglyceride levels (UKB data field 30870) (CNV mirror model) 316,681 white British ancestry individuals NA NR [28257] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90027317 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Total protein levels (UKB data field 30860) (CNV mirror model) 290,746 white British ancestry individuals NA NR [28257] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90027318 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Waist-hip ratio (UKB data field 49/48) (CNV mirror model) 330,926 white British ancestry individuals NA NR [28257] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90027324 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Waist-to-hip ratio adjusted for BMI (UKB data field 49/48) (CNV mirror model) 330,414 white British ancestry individuals NA NR [28257] 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90027325 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Balding (UKB data field 2395) (CNV mirror model) 152,044 white British ancestry males NA NR [28257] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90027326 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. High density lipoprotein cholesterol levels (UKB data field 30760) (CNV duplication-only model) 290,940 white British ancestry individuals NA NR [14070] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90027356 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Birth weight of first child (UKB data field 2744) (CNV mirror model) 143,630 white British ancestry females NA NR [28257] 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90027328 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Age at menarche (UKB data field 2714) (CNV mirror model) 173,725 white British ancestry females NA NR [28257] 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90027329 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Age at menopause (UKB data field 3581) (CNV mirror model) 105,469 white British ancestry females NA NR [28257] 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90027330 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Albumin levels (UKB data field 30600) (CNV duplication-only model) 291,060 white British ancestry individuals NA NR [14070] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90027331 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Mean corpuscular haemoglobin (UKB data field 30050) (CNV duplication-only model) 322,496 white British ancestry individuals NA NR [14070] 0 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90027363 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Monocyte count (UKB data field 30130) (CNV duplication-only model) 321,953 white British ancestry individuals NA NR [14070] 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90027364 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Neuroticism (UKB data field 20127) (CNV duplication-only model) 269,539 white British ancestry individuals NA NR [14070] 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90027365 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Neutrophill count (UKB data field 30140) (CNV duplication-only model) 321,953 white British ancestry individuals NA NR [14070] 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90027366 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Phosphate levels (UKB data field 30810) (CNV duplication-only model) 290,512 white British ancestry individuals NA NR [14070] 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90027367 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Platelet count (UKB data field 30080) (CNV duplication-only model) 322,499 white British ancestry individuals NA NR [14070] 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90027368 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Red blood cell erythrocyte count (UKB data field 30010) (CNV duplication-only model) 322,500 white British ancestry individuals NA NR [14070] 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90027369 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Reticulocyte count (UKB data field 30250) (CNV duplication-only model) 317,487 white British ancestry individuals NA NR [14070] 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90027370 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Aspartate aminotransferase levels (UKB data field 30650) (CNV duplication-only model) 315,807 white British ancestry individuals NA NR [14070] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90027336 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Total bilirubin levels (UKB data field 30840) (CNV duplication-only model) 315,664 white British ancestry individuals NA NR [14070] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90027337 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Birth weight (UKB data field 20022) (CNV duplication-only model) 192,408 white British ancestry individuals NA NR [14070] 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90027338 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Heel bone mineral density (UKB data field 3148) (CNV duplication-only model) 191,028 white British ancestry individuals NA NR [14070] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90027339 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Body mass index (UKB data field 21001) (CNV duplication-only model) 330,497 white British ancestry individuals NA NR [14070] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90027340 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Basal metabolic rate (UKB data field 23105) (CNV duplication-only model) 325,954 white British ancestry individuals NA NR [14070] 0 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST90027341 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Whole body fat mass (UKB data field 23100) (CNV duplication-only model) 325,438 white British ancestry individuals NA NR [14070] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90027342 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Calcium levels (UKB data field 30680) (CNV duplication-only model) 290,951 white British ancestry individuals NA NR [14070] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90027343 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Cholesterol levels (UKB data field 30690) (CNV duplication-only model) 316,939 white British ancestry individuals NA NR [14070] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90027344 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Triglyceride levels (UKB data field 30870) (CNV duplication-only model) 316,681 white British ancestry individuals NA NR [14070] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90027374 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Total protein levels (UKB data field 30860) (CNV duplication-only model) 290,746 white British ancestry individuals NA NR [14070] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90027375 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Urate levels (UKB data field 30880) (CNV duplication-only model) 316,545 white British ancestry individuals NA NR [14070] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90027376 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Urea levels (UKB data field 30670) (CNV duplication-only model) 316,737 white British ancestry individuals NA NR [14070] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90027377 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Vitamin D levels (UKB data field 30890) (CNV duplication-only model) 303,212 white British ancestry individuals NA NR [14070] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90027378 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. White blood cell leukocyte count (UKB data field 30000) (CNV duplication-only model) 322,497 white British ancestry individuals NA NR [14070] 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90027379 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Weight (UKB data field 21002) (CNV duplication-only model) 330,607 white British ancestry individuals NA NR [14070] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90027380 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Waist-hip ratio (UKB data field 49/48) (CNV duplication-only model) 330,926 white British ancestry individuals NA NR [14070] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90027381 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Waist-to-hip ratio adjusted for BMI (UKB data field 49/48) (CNV duplication-only model) 330,414 white British ancestry individuals NA NR [14070] 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90027382 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Balding (UKB data field 2395) (CNV duplication-only model) 152,044 white British ancestry males NA NR [14070] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90027383 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Relative age of first facial hair (UKB data field 2375) (CNV duplication-only model) 148,371 white British ancestry males NA NR [14070] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90027384 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Birth weight of first child (UKB data field 2744) (CNV duplication-only model) 143,630 white British ancestry females NA NR [14070] 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90027385 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Age at menarche (UKB data field 2714) (CNV duplication-only model) 173,725 white British ancestry females NA NR [14070] 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90027386 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Age at menopause (UKB data field 3581) (CNV duplication-only model) 105,469 white British ancestry females NA NR [14070] 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90027387 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Albumin levels (UKB data field 30600) (CNV deletion-only model) 291,060 white British ancestry individuals NA NR [9936] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90027388 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Alkaline phosphatase levels (UKB data field 30610) (CNV deletion-only model) 316,951 white British ancestry individuals NA NR [9936] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90027389 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Alanine aminotransferase levels (UKB data field 30620) (CNV deletion-only model) 316,815 white British ancestry individuals NA NR [9936] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90027390 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Apolipoprotein A levels (UKB data field 30630) (CNV deletion-only model) 289,352 white British ancestry individuals NA NR [9936] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90027391 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Apolipoprotein B levels (UKB data field 30640) (CNV deletion-only model) 315,444 white British ancestry individuals NA NR [9936] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90027392 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Aspartate aminotransferase levels (UKB data field 30650) (CNV deletion-only model) 315,807 white British ancestry individuals NA NR [9936] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90027393 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Total bilirubin levels (UKB data field 30840) (CNV deletion-only model) 315,664 white British ancestry individuals NA NR [9936] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90027394 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Birth weight (UKB data field 20022) (CNV deletion-only model) 192,408 white British ancestry individuals NA NR [9936] 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90027395 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Heel bone mineral density (UKB data field 3148) (CNV deletion-only model) 191,028 white British ancestry individuals NA NR [9936] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90027396 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Body mass index (UKB data field 21001) (CNV deletion-only model) 330,497 white British ancestry individuals NA NR [9936] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90027397 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Basal metabolic rate (UKB data field 23105) (CNV deletion-only model) 325,954 white British ancestry individuals NA NR [9936] 0 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST90027398 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Creatinine levels (UKB data field 30700) (CNV duplication-only model) 316,786 white British ancestry individuals NA NR [14070] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90027345 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. C reactive protein levels (UKB data field 30710) (CNV duplication-only model) 316,278 white British ancestry individuals NA NR [14070] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90027346 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Cystatin C levels (UKB data field 30720) (CNV duplication-only model) 316,915 white British ancestry individuals NA NR [14070] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90027347 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Diastolic blood pressure automated reading (UKB data field 4079) (CNV duplication-only model) 313,183 white British ancestry individuals NA NR [14070] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90027348 Genome-wide genotyping array 2022-08-04 34837083 Pirruccello JP 2021-11-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34837083 Deep learning enables genetic analysis of the human thoracic aorta. Ascending thoracic aortic diameter 33,637 European ancestry individuals, 5,057 individuals NA Affymetrix [16646699] (imputed) 82 ascending aortic diameter http://www.ebi.ac.uk/efo/EFO_0021787 GCST90094400 Genome-wide genotyping array 2022-08-04 34837083 Pirruccello JP 2021-11-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34837083 Deep learning enables genetic analysis of the human thoracic aorta. Descending thoracic aortic diameter 34,532 European ancestry individuals, 5,156 individuals NA Affymetrix [16646699] (imputed) 47 descending aortic diameter http://www.ebi.ac.uk/efo/EFO_0021788 GCST90094401 Genome-wide genotyping array 2022-08-04 34837083 Pirruccello JP 2021-11-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34837083 Deep learning enables genetic analysis of the human thoracic aorta. Ascending thoracic aortic diameter 33,637 European ancestry individuals NA Affymetrix [NR] (imputed) 67 ascending aortic diameter http://www.ebi.ac.uk/efo/EFO_0021787 GCST90094402 Genome-wide genotyping array 2022-08-04 34837083 Pirruccello JP 2021-11-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34837083 Deep learning enables genetic analysis of the human thoracic aorta. Descending thoracic aortic diameter 34,532 European ancestry individuals NA Affymetrix [NR] (imputed) 37 descending aortic diameter http://www.ebi.ac.uk/efo/EFO_0021788 GCST90094403 Genome-wide genotyping array 2022-09-14 35999565 Chen W 2022-08-23 BMC Med www.ncbi.nlm.nih.gov/pubmed/35999565 Genetic predispositions to psychiatric disorders and the risk of COVID-19. Depression 6,854 White ancestry individuals NA Affymetrix [NR] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90134640 Genome-wide genotyping array 2022-09-14 35999565 Chen W 2022-08-23 BMC Med www.ncbi.nlm.nih.gov/pubmed/35999565 Genetic predispositions to psychiatric disorders and the risk of COVID-19. Anxiety 5,166 White ancestry individuals NA Affymetrix [NR] (imputed) 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90134641 Genome-wide genotyping array 2022-09-14 35999565 Chen W 2022-08-23 BMC Med www.ncbi.nlm.nih.gov/pubmed/35999565 Genetic predispositions to psychiatric disorders and the risk of COVID-19. Psychotic disorder 384 White ancestry individuals NA Affymetrix [NR] (imputed) 0 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST90134642 Genome-wide genotyping array 2022-09-14 35999565 Chen W 2022-08-23 BMC Med www.ncbi.nlm.nih.gov/pubmed/35999565 Genetic predispositions to psychiatric disorders and the risk of COVID-19. Stress-related disorders 268 White ancestry individuals NA Affymetrix [NR] (imputed) 0 stress-related disorder http://www.ebi.ac.uk/efo/EFO_0010098 GCST90134643 Genome-wide genotyping array 2022-09-14 35999565 Chen W 2022-08-23 BMC Med www.ncbi.nlm.nih.gov/pubmed/35999565 Genetic predispositions to psychiatric disorders and the risk of COVID-19. Substance misuse 7,118 White ancestry individuals NA Affymetrix [NR] (imputed) 0 substance abuse http://purl.obolibrary.org/obo/MONDO_0002491 GCST90134639 Genome-wide genotyping array 2022-08-05 35831902 Chiou JS 2022-07-13 BMC Med www.ncbi.nlm.nih.gov/pubmed/35831902 Your height affects your health: genetic determinants and health-related outcomes in Taiwan. Height 67,452 Han Chinese ancestry individuals NA Affymetrix [NR] (imputed) 433 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90131910 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Cardiovascular death or hospitalisation in heart failure 2,727 European ancestry individuals NA Illumina [5140623] (imputed) 0 cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0006919 GCST90134309 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Cardiovascular death or hospitalisation in heart failure 1,698 European ancestry individuals NA Illumina [5140623] (imputed) 0 cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0006919 GCST90134310 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Cardiovascular death or hospitalisation in heart failure 1,029 European ancestry individuals NA Illumina [5140623] (imputed) 1 cardiovascular event measurement http://www.ebi.ac.uk/efo/EFO_0006919 GCST90134311 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Cardiovascular death or hospitalisation in heart failure treated with candesartan 1,371 European ancestry individuals NA Illumina [5140623] (imputed) 1 response to candesartan, cardiovascular event measurement http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0006919 GCST90134312 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Cardiovascular death or hospitalisation in heart failure treated with candesartan 860 European ancestry individuals NA Illumina [5140623] (imputed) 1 response to candesartan, cardiovascular event measurement http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0006919 GCST90134313 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Cardiovascular death or hospitalisation in heart failure treated with candesartan 511 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, cardiovascular event measurement http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0006919 GCST90134314 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Hyperkalemia in heart failure treated with candesartan 1,371 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, Hyperkalemia http://purl.obolibrary.org/obo/GO_1901556, http://purl.obolibrary.org/obo/HP_0002153 GCST90134315 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Hyperkalemia in heart failure treated with candesartan 860 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, Hyperkalemia http://purl.obolibrary.org/obo/GO_1901556, http://purl.obolibrary.org/obo/HP_0002153 GCST90134316 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Hyperkalemia in heart failure treated with candesartan 511 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, Hyperkalemia http://purl.obolibrary.org/obo/GO_1901556, http://purl.obolibrary.org/obo/HP_0002153 GCST90134317 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Renal dysfunction in heart failure treated with candesartan 1,371 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, impaired renal function disease http://purl.obolibrary.org/obo/GO_1901556, http://purl.obolibrary.org/obo/MONDO_0001343 GCST90134318 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Renal dysfunction in heart failure treated with candesartan 860 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, impaired renal function disease http://purl.obolibrary.org/obo/GO_1901556, http://purl.obolibrary.org/obo/MONDO_0001343 GCST90134319 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Renal dysfunction in heart failure treated with candesartan 511 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, impaired renal function disease http://purl.obolibrary.org/obo/GO_1901556, http://purl.obolibrary.org/obo/MONDO_0001343 GCST90134320 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Hypotension in heart failure treated with candesartan 1,371 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, hypotension http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0005251 GCST90134321 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Hypotension in heart failure treated with candesartan 860 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, hypotension http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0005251 GCST90134322 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Hypotension in heart failure treated with candesartan 511 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, hypotension http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0005251 GCST90134323 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Change in SBP after 6 weeks in heart failure treated with candesartan 1,285 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0006944 GCST90134324 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Change in SBP after 6 weeks in heart failure treated with candesartan 805 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0006944 GCST90134325 Genome-wide genotyping array 2022-09-02 35736394 Dube MP 2022-06-23 ESC Heart Fail www.ncbi.nlm.nih.gov/pubmed/35736394 Pharmacogenomic study of heart failure and candesartan response from the CHARM programme. Change in SBP after 6 weeks in heart failure treated with candesartan 480 European ancestry individuals NA Illumina [5140623] (imputed) 0 response to candesartan, systolic blood pressure change measurement http://purl.obolibrary.org/obo/GO_1901556, http://www.ebi.ac.uk/efo/EFO_0006944 GCST90134326 Genome-wide genotyping array 2022-09-20 35939300 Chen C 2022-08-01 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/35939300 Association of Single-Nucleotide Variants in the Human Leukocyte Antigen and Other Loci With Childhood Hodgkin Lymphoma. Hodgkin's lymphoma 1,286 European ancestry cases, 6,193 European ancestry non-Hodgkin lymphoma childhood cancer cases, 369 European ancestry non-cancer controls NA Illumina [6880000] (imputed) 8 Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183 GCST90134660 Genome-wide genotyping array, Genome-wide sequencing 2023-01-05 35671886 Vernet R 2022-06-04 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/35671886 Identification of novel genes influencing eosinophil-specific protein levels in asthma families. Eosinophil cationic protein levels 1,018 European ancestry individuals 153 French-Canadian founder ancestry individuals Illumina [7035638] (imputed) 1 eosinophil cationic protein measurement http://www.ebi.ac.uk/efo/EFO_0010913 GCST90244022 Genome-wide genotyping array 2023-01-05 35671886 Vernet R 2022-06-04 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/35671886 Identification of novel genes influencing eosinophil-specific protein levels in asthma families. Eosinophil-derived neurotoxin levels 1,018 European ancestry individuals 153 French-Canadian founder ancestry individuals Illumina [7035638] (imputed) 3 eosinophil-derived neurotoxin measurement http://www.ebi.ac.uk/efo/EFO_0022048 GCST90244023 Genome-wide genotyping array 2023-01-05 35671886 Vernet R 2022-06-04 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/35671886 Identification of novel genes influencing eosinophil-specific protein levels in asthma families. Eosinophil cationic protein levels and Eosinophil-derived neurotoxin levels 1,018 European ancestry individuals 153 French-Canadian founder ancestry individuals Illumina [7035638] (imputed) 2 eosinophil cationic protein measurement, eosinophil-derived neurotoxin measurement http://www.ebi.ac.uk/efo/EFO_0010913, http://www.ebi.ac.uk/efo/EFO_0022048 GCST90244024 Genome-wide genotyping array 2022-09-06 35837121 Gloor Y 2022-06-28 Front Neurosci www.ncbi.nlm.nih.gov/pubmed/35837121 Uncovering a Genetic Polymorphism Located in Huntingtin Associated Protein 1 in Modulation of Central Pain Sensitization Signaling Pathways. Nociceptive flexion reflex threshold 212 European ancestry fibromyalgia syndrome patients, 72 European ancestry healthy controls NA Illumina [258756] 1 nociceptive flexion reflex threshold http://www.ebi.ac.uk/efo/EFO_0021813 GCST90134341 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Aspartic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [166626] 0 aspartic acid measurement http://www.ebi.ac.uk/efo/EFO_0801113 GCST90176088 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Atenolol levels 2,466 Black/admixed ancestry individuals NA Illumina [169492] 0 atenolol measurement http://www.ebi.ac.uk/efo/EFO_0801114 GCST90178919 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Atorvastatin levels 2,466 Black/admixed ancestry individuals NA Illumina [178075] 0 atorvastatin measurement http://www.ebi.ac.uk/efo/EFO_0801115 GCST90176123 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. ATP levels 2,466 Black/admixed ancestry individuals NA Illumina [151932] 0 ATP measurement http://www.ebi.ac.uk/efo/EFO_0801116 GCST90176036 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Betaine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153327] 1 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90176157 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Bilirubin levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158624] 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90176037 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Bilirubin levels 2,466 Black/admixed ancestry individuals NA Illumina [151271] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90176158 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Biliverdin levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153465] 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90176159 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Butyric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [166697] 0 butyric acid measurement http://www.ebi.ac.uk/efo/EFO_0801117 GCST90176114 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Butyrobetaine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156417] 2 butyrobetaine measurement http://www.ebi.ac.uk/efo/EFO_0801118 GCST90176160 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C10 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156693] 2 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90176161 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C10:2 levels 2,466 Black/admixed ancestry individuals NA Illumina [168296] 0 C10:2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801119 GCST90176162 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C12 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152442] 2 dodecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021804 GCST90176163 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C12:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [152185] 0 dodecenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021808 GCST90176164 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C14 levels 2,466 Black/admixed ancestry individuals NA Illumina [152666] 0 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90176165 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (14:0) levels 2,466 Black/admixed ancestry individuals NA Illumina [155847] 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90176166 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Sphingomyelin C14:0 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152421] 1 C14:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801120 GCST90176167 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C14:1 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152448] 1 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90176168 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C14:2 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154114] 1 C14:2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801121 GCST90176169 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C16 levels 2,466 Black/admixed ancestry individuals NA Illumina [153784] 0 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90176170 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Ceramide (d18:1/16:0) levels 2,466 Black/admixed ancestry individuals NA Illumina [150634] 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90176171 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamines (16:0) levels 2,466 Black/admixed ancestry individuals NA Illumina [153434] 0 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90176172 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Sphingomyeline C16:0 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152261] 1 sphingomyelin 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010391 GCST90176173 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (16:1) levels 2,466 Black/admixed ancestry individuals NA Illumina [158796] 0 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90176174 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholine plasmalogen C16:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [157897] 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90176175 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 1,7-dimethyluric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [159051] 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90176134 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 1,7-dimethyluric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [150508] 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90178714 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 11(12)-EET levels 2,466 Black/admixed ancestry individuals NA Illumina [153926] 0 11(12)-EET measurement http://www.ebi.ac.uk/efo/EFO_0801096 GCST90176107 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 12-Oxo-ETE levels 2,466 Black/admixed ancestry individuals NA Illumina [148311] 0 12-oxo-ETE measurement http://www.ebi.ac.uk/efo/EFO_0801097 GCST90176108 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 14(15)-EET levels 2,466 Black/admixed ancestry individuals NA Illumina [158379] 0 14(15)-EET measurement http://www.ebi.ac.uk/efo/EFO_0801098 GCST90176109 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 15-Oxo-ETE levels 2,466 Black/admixed ancestry individuals NA Illumina [156471] 0 15-oxo-ETE measurement http://www.ebi.ac.uk/efo/EFO_0801099 GCST90176110 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-aminoadipic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [153438] 0 aminoadipic acid measurement http://www.ebi.ac.uk/efo/EFO_0010459 GCST90176023 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-aminoisobutyric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [156768] 0 2-aminoisobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0801100 GCST90176135 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-aminooctanoate levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154538] 1 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90176136 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI3127) 2,466 Black/admixed ancestry individuals NA Illumina [143578] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176024 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2'-deoxyuridine levels 2,466 Black/admixed ancestry individuals NA Illumina [150149] 0 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90176137 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-hydroxybutyric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [155667] 0 alpha-hydroxybutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0010458 GCST90176025 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-hydroxyglutaric acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160831] 2 2-hydroxyglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0010446 GCST90176026 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-hydroxyhippurate levels 2,466 Black/admixed ancestry individuals NA Illumina [153328] 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90176138 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-hydroxyhippurate levels 2,466 Black/admixed ancestry individuals NA Illumina [160730] 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90178715 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 2-ketoisovaleric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [161135] 0 2-ketoisovaleric acid measurement http://www.ebi.ac.uk/efo/EFO_0801101 GCST90176086 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 20-hydroxy-N-arachidonoyl taurine levels 2,466 Black/admixed ancestry individuals NA Illumina [161752] 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90176111 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 3-(N-acetyl-L-cystein-S-yl) acetaminophen levels 2,466 Black/admixed ancestry individuals NA Illumina [149270] 0 3-cystein-S-ylacetaminophen measurement http://www.ebi.ac.uk/efo/EFO_0021155 GCST90176139 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 3-(N-acetyl-L-cystein-S-yl) acetaminophen levels 2,466 Black/admixed ancestry individuals NA Illumina [148371] 0 3-cystein-S-ylacetaminophen measurement http://www.ebi.ac.uk/efo/EFO_0021155 GCST90178917 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 3-hydroxybutyric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [155114] 0 3-hydroxybutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0010113 GCST90176027 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 3-hydroxyhippurate levels 2,466 Black/admixed ancestry individuals NA Illumina [160361] 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90176140 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 4-acetamidobutanoate levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155120] 1 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90176141 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 4-aminohippuric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [151944] 0 4-aminohippuric acid measurement http://www.ebi.ac.uk/efo/EFO_0801102 GCST90176142 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 4-hydroxy-3-methylacetophenone levels 2,466 Black/admixed ancestry individuals NA Illumina [155210] 0 4-hydroxy-3-methylacetophenone measurement http://www.ebi.ac.uk/efo/EFO_0801103 GCST90176143 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 5-hydroxytryptophol levels 2,466 Black/admixed ancestry individuals NA Illumina [155772] 0 5-hydroxytryptophol measurement http://www.ebi.ac.uk/efo/EFO_0801104 GCST90176144 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (22:4) levels 2,466 Black/admixed ancestry individuals NA Illumina [151782] 0 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90176201 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (22:5) levels 2,466 Black/admixed ancestry individuals NA Illumina [152941] 0 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90176202 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (22:6) levels 2,466 Black/admixed ancestry individuals NA Illumina [154135] 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90176203 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamines (22:6) levels 2,466 Black/admixed ancestry individuals NA Illumina [153329] 0 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90176204 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholine C24:0 levels 2,466 Black/admixed ancestry individuals NA Illumina [149594] 0 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90176205 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Ceramide (d18:1/24:1) levels 2,466 Black/admixed ancestry individuals NA Illumina [150401] 0 lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800517 GCST90176206 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Cerotoylcarnitine (C26) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156681] 1 cerotoylcarnitine (C26) measurement http://www.ebi.ac.uk/efo/EFO_0800542 GCST90176207 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Propionylcarnitine (c3) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152249] 1 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90176209 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. CAR DC3:0;2Me levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157881] 1 C3-DC-CH3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801128 GCST90176208 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholines (30:0) levels 2,466 Black/admixed ancestry individuals NA Illumina [152047] 0 C30:0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0801129 GCST90176210 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine (32:2) levels 2,466 Black/admixed ancestry individuals NA Illumina [151173] 0 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90176211 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine C34:0 levels 2,466 Black/admixed ancestry individuals NA Illumina [149783] 0 C34:0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801130 GCST90176212 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. DAG NH4 C34:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [148655] 0 C34:1 DAG NH4 measurement http://www.ebi.ac.uk/efo/EFO_0801131 GCST90176213 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine (34:2) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159902] 1 C34:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801132 GCST90176214 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine plasmalogen C34:2 levels 2,466 Black/admixed ancestry individuals NA Illumina [154196] 0 C34:2 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801133 GCST90176215 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine C34:3 levels 2,466 Black/admixed ancestry individuals NA Illumina [151638] 0 phosphatidylcholine 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0010377 GCST90176216 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine plasmalogen C34:3 levels 2,466 Black/admixed ancestry individuals NA Illumina [153097] 0 C34:3 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801134 GCST90176217 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine plasmalogen C34:3 levels 2,466 Black/admixed ancestry individuals NA Illumina [151886] 0 C34:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801135 GCST90176218 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine 34:4 levels 2,466 Black/admixed ancestry individuals NA Illumina [152542] 0 phosphatidylcholine 34:4 measurement http://www.ebi.ac.uk/efo/EFO_0010378 GCST90176219 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine C36:2 levels 2,466 Black/admixed ancestry individuals NA Illumina [151304] 0 phosphatidylcholine 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010380 GCST90176220 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine (36:2) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157720] 1 C36:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801136 GCST90176221 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylserine plasmalogen C36:2 levels 2,466 Black/admixed ancestry individuals NA Illumina [152096] 0 C36:2 phosphatidylserine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801137 GCST90176222 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine (36:3) levels 2,466 Black/admixed ancestry individuals NA Illumina [149906] 0 C36:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801138 GCST90176223 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylserine plasmalogen C36:3 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155460] 1 C36:3 phosphatidylserine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801139 GCST90176224 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine 36:4 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160396] 1 C36:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801140 GCST90176225 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 5-MTHF levels 2,466 Black/admixed ancestry individuals NA Illumina [142960] 0 5-MTHF measurement http://www.ebi.ac.uk/efo/EFO_0801105 GCST90176112 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 5-Oxo-ETE levels 2,466 Black/admixed ancestry individuals NA Illumina [146593] 0 5-oxo-ETE measurement http://www.ebi.ac.uk/efo/EFO_0801106 GCST90176113 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 7-methylguanine levels 2,466 Black/admixed ancestry individuals NA Illumina [159171] 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90176145 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. A-Ketoglutaric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [163801] 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90176032 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Acetaminophen glucuronide levels 2,466 Black/admixed ancestry individuals NA Illumina [156857] 0 acetaminophen glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801107 GCST90176147 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Acetaminophen glucuronide levels 2,466 Black/admixed ancestry individuals NA Illumina [154092] 0 acetaminophen glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801107 GCST90178918 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Acetaminophen levels 2,466 Black/admixed ancestry individuals NA Illumina [176815] 0 acetaminophen measurement http://www.ebi.ac.uk/efo/EFO_0801108 GCST90176146 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Acetoacetic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [166470] 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90176028 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Acetylglutamic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [160081] 0 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90176148 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Acisoga levels 2,466 Black/admixed ancestry individuals NA Illumina [153654] 0 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90176149 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Aconitic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [158245] 0 aconitic acid measurement http://www.ebi.ac.uk/efo/EFO_0801109 GCST90176029 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Adipic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [142786] 0 Adipic acid measurement http://www.ebi.ac.uk/efo/EFO_0021575 GCST90176030 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. ADMA levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163521] 1 asymmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006522 GCST90176150 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. ADP levels 2,466 Black/admixed ancestry individuals NA Illumina [148856] 0 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90176031 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Alanine levels 2,466 Black/admixed ancestry individuals NA Illumina [156279] 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90176151 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Allantoin levels 2,466 Black/admixed ancestry individuals NA Illumina [153830] 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90176033 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Allantoin levels 2,466 Black/admixed ancestry individuals NA Illumina [152373] 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90176152 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Alpha-glycerophosphocholine levels 2,466 Black/admixed ancestry individuals NA Illumina [154983] 0 alpha-glycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0801110 GCST90176153 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. AMP levels 2,466 Black/admixed ancestry individuals NA Illumina [155027] 0 Cyclic AMP measurement http://www.ebi.ac.uk/efo/EFO_0021580 GCST90176034 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Anthranilic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [153953] 0 anthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0010460 GCST90176035 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Arachidonic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [160847] 0 arachidonic acid measurement http://www.ebi.ac.uk/efo/EFO_0006808 GCST90176099 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Arachindonoyl phenylalanine levels 2,466 Black/admixed ancestry individuals NA Illumina [161604] 0 arachindonoyl phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0801111 GCST90176087 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Arecaidine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [168262] 4 arecaidine measurement http://www.ebi.ac.uk/efo/EFO_0801112 GCST90176154 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Arginine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152820] 1 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90176155 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Asparagine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153063] 2 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90176156 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Sphingomyeline C16:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [147566] 0 sphingomyelin 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010392 GCST90176176 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C18 levels 2,466 Black/admixed ancestry individuals NA Illumina [153251] 0 C18 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801122 GCST90176177 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (18:0) levels 2,466 Black/admixed ancestry individuals NA Illumina [156534] 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90176178 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamines (18:0) levels 2,466 Black/admixed ancestry individuals NA Illumina [154669] 0 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90176179 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamines (18:0) levels 2,466 Black/admixed ancestry individuals NA Illumina [152582] 0 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90176180 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Sphingomyeline C18:0 levels 2,466 Black/admixed ancestry individuals NA Illumina [151766] 0 sphingomyelin 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010393 GCST90176181 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C18:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [155454] 0 C18:1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801123 GCST90176182 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (18:1) levels 2,466 Black/admixed ancestry individuals NA Illumina [155127] 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90176183 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholine plasmalogen C18:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [161915] 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90176184 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholine plasmalogen minor C18:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [170040] 0 lysophosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010224 GCST90176185 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamine C18:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [167556] 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90176186 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Sphingomyeline C18:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [150659] 0 sphingomyelin 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010394 GCST90176187 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C18:2 levels 2,466 Black/admixed ancestry individuals NA Illumina [152317] 0 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90176188 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (18:2) levels 2,466 Black/admixed ancestry individuals NA Illumina [152904] 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90176189 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamines (18:2) levels 2,466 Black/admixed ancestry individuals NA Illumina [150476] 0 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90176190 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (18:3) levels 2,466 Black/admixed ancestry individuals NA Illumina [156632] 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90176191 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamine C18:3 levels 2,466 Black/admixed ancestry individuals NA Illumina [163704] 0 C18:3 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801124 GCST90176192 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Acetylcarnitine (c2) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [147995] 1 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90176193 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamine C20:0 levels 2,466 Black/admixed ancestry individuals NA Illumina [152675] 0 C20:0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801125 GCST90176194 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Sphingomyelin C20:0 levels 2,466 Black/admixed ancestry individuals NA Illumina [154873] 0 C20:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801126 GCST90176195 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (20:1) levels 2,466 Black/admixed ancestry individuals NA Illumina [153362] 0 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90176196 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamine C20:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [152087] 0 C20:1 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801127 GCST90176197 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholine 20:4 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160106] 1 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90176198 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylethanolamines (20:4) levels 2,466 Black/admixed ancestry individuals NA Illumina [155514] 0 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90176199 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysophosphatidylcholines (20:5) levels 2,466 Black/admixed ancestry individuals NA Illumina [153006] 0 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90176200 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11942) 2,466 Black/admixed ancestry individuals NA Illumina [167072] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176577 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11942) 2,466 Black/admixed ancestry individuals NA Illumina [152621] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178745 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11944) 2,466 Black/admixed ancestry individuals NA Illumina [158291] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176578 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11949) 2,466 Black/admixed ancestry individuals NA Illumina [150367] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176579 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1195) 2,466 Black/admixed ancestry individuals NA Illumina [150868] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176580 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11967) 2,466 Black/admixed ancestry individuals NA Illumina [152415] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176581 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1197) 2,466 Black/admixed ancestry individuals NA Illumina [175053] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176582 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11976) 2,466 Black/admixed ancestry individuals NA Illumina [153377] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176583 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11989) 2,466 Black/admixed ancestry individuals NA Illumina [156013] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176584 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11992) 2,466 Black/admixed ancestry individuals NA Illumina [155857] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176585 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11992) 2,466 Black/admixed ancestry individuals NA Illumina [147136] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178971 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1200) 2,466 Black/admixed ancestry individuals NA Illumina [151988] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176586 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12000) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155911] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176587 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12018) 2,466 Black/admixed ancestry individuals NA Illumina [157533] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176588 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1202) 2,466 Black/admixed ancestry individuals NA Illumina [157691] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176589 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12025) 2,466 Black/admixed ancestry individuals NA Illumina [152381] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176590 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12025) 2,466 Black/admixed ancestry individuals NA Illumina [153107] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178746 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12033) 2,466 Black/admixed ancestry individuals NA Illumina [150068] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176591 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1204) 2,466 Black/admixed ancestry individuals NA Illumina [157145] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176592 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N1-methyladenosine levels 2,466 Black/admixed ancestry individuals NA Illumina [156752] 0 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90176129 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 1-methylguanidine levels 2,466 Black/admixed ancestry individuals NA Illumina [150877] 0 1-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0801093 GCST90176130 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 1-methylguanosine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154662] 1 1-methylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0801094 GCST90176131 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 1-methylhistamine levels 2,466 Black/admixed ancestry individuals NA Illumina [149837] 0 1-methylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0801095 GCST90176132 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 1-methylnicotinamide levels 2,466 Black/admixed ancestry individuals NA Illumina [157741] 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90176133 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. 1,5-AG / 1-deoxyglucose levels 2,466 Black/admixed ancestry individuals NA Illumina [170320] 0 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90104476 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11745) 2,466 Black/admixed ancestry individuals NA Illumina [152693] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178742 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11749) 2,466 Black/admixed ancestry individuals NA Illumina [163545] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176557 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11754) 2,466 Black/admixed ancestry individuals NA Illumina [160136] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176558 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11754) 2,466 Black/admixed ancestry individuals NA Illumina [150485] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178743 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11756) 2,466 Black/admixed ancestry individuals NA Illumina [154715] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176559 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11775) 2,466 Black/admixed ancestry individuals NA Illumina [165528] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176560 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI118) 2,466 Black/admixed ancestry individuals NA Illumina [150077] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176561 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI118) 2,466 Black/admixed ancestry individuals NA Illumina [151571] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178969 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11802) 2,466 Black/admixed ancestry individuals NA Illumina [150869] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176562 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11811) 2,466 Black/admixed ancestry individuals NA Illumina [157007] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176563 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11811) 2,466 Black/admixed ancestry individuals NA Illumina [159286] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178744 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1183) 2,466 Black/admixed ancestry individuals NA Illumina [149165] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176564 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11833) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149251] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176565 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11886) 2,466 Black/admixed ancestry individuals NA Illumina [153016] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176566 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1189) 2,466 Black/admixed ancestry individuals NA Illumina [164499] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176567 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11890) 2,466 Black/admixed ancestry individuals NA Illumina [151560] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176568 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1190) 2,466 Black/admixed ancestry individuals NA Illumina [157121] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176569 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11906) 2,466 Black/admixed ancestry individuals NA Illumina [171130] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176570 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1191) 2,466 Black/admixed ancestry individuals NA Illumina [149181] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176571 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1192) 2,466 Black/admixed ancestry individuals NA Illumina [154174] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176572 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11924) 2,466 Black/admixed ancestry individuals NA Illumina [155067] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176573 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11927) 2,466 Black/admixed ancestry individuals NA Illumina [149912] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176574 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11927) 2,466 Black/admixed ancestry individuals NA Illumina [140653] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178970 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11936) 2,466 Black/admixed ancestry individuals NA Illumina [153906] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176575 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1194) 2,466 Black/admixed ancestry individuals NA Illumina [157983] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176576 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1308) 2,466 Black/admixed ancestry individuals NA Illumina [149064] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176701 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13145) 2,466 Black/admixed ancestry individuals NA Illumina [150303] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176702 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13147) 2,466 Black/admixed ancestry individuals NA Illumina [161789] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176703 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1322) 2,466 Black/admixed ancestry individuals NA Illumina [145601] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176704 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13235) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162710] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176705 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13252) 2,466 Black/admixed ancestry individuals NA Illumina [160230] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176706 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13299) 2,466 Black/admixed ancestry individuals NA Illumina [148398] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176707 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13322) 2,466 Black/admixed ancestry individuals NA Illumina [172798] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176708 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13322) 2,466 Black/admixed ancestry individuals NA Illumina [152677] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178755 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13326) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152703] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176709 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13343) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159905] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176710 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13355) 2,466 Black/admixed ancestry individuals NA Illumina [161969] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176711 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13355) 2,466 Black/admixed ancestry individuals NA Illumina [169481] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178756 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13360) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163642] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176712 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13371) 2,466 Black/admixed ancestry individuals NA Illumina [157220] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176713 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13371) 2,466 Black/admixed ancestry individuals NA Illumina [162879] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178757 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13374) 2,466 Black/admixed ancestry individuals NA Illumina [155195] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176714 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13374) 2,466 Black/admixed ancestry individuals NA Illumina [151834] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178980 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13375) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160771] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176715 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1338) 2,466 Black/admixed ancestry individuals NA Illumina [167640] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176716 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13382) 2,466 Black/admixed ancestry individuals NA Illumina [166110] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176717 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13385) 2,466 Black/admixed ancestry individuals NA Illumina [156661] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176718 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13389) 2,466 Black/admixed ancestry individuals NA Illumina [175259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176719 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1339) 2,466 Black/admixed ancestry individuals NA Illumina [152919] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176720 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13392) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154037] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176721 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6440) 2,466 Black/admixed ancestry individuals NA Illumina [167691] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178103 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6441) 2,466 Black/admixed ancestry individuals NA Illumina [172701] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178104 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6442) 2,466 Black/admixed ancestry individuals NA Illumina [155827] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178105 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6443) 2,466 Black/admixed ancestry individuals NA Illumina [160373] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178106 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6446) 2,466 Black/admixed ancestry individuals NA Illumina [148887] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178107 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6447) 2,466 Black/admixed ancestry individuals NA Illumina [161232] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178108 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6455) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153699] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178109 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6460) 2,466 Black/admixed ancestry individuals NA Illumina [153495] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178110 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6462) 2,466 Black/admixed ancestry individuals NA Illumina [171231] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178111 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6462) 2,466 Black/admixed ancestry individuals NA Illumina [152269] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179084 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6468) 2,466 Black/admixed ancestry individuals NA Illumina [151406] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178112 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6469) 2,466 Black/admixed ancestry individuals NA Illumina [159723] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178113 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6469) 2,466 Black/admixed ancestry individuals NA Illumina [166963] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178887 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12693) 2,466 Black/admixed ancestry individuals NA Illumina [154700] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176669 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12706) 2,466 Black/admixed ancestry individuals NA Illumina [154109] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176670 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12720) 2,466 Black/admixed ancestry individuals NA Illumina [154953] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176671 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12720) 2,466 Black/admixed ancestry individuals NA Illumina [164457] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178753 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12731) 2,466 Black/admixed ancestry individuals NA Illumina [149826] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176672 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12743) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151435] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176673 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12750) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [175266] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176674 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1276) 2,466 Black/admixed ancestry individuals NA Illumina [148901] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176675 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12764) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150320] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176676 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12768) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161726] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176677 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12778) 2,466 Black/admixed ancestry individuals NA Illumina [155048] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176678 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12791) 2,466 Black/admixed ancestry individuals NA Illumina [162935] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176679 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13618) 2,466 Black/admixed ancestry individuals NA Illumina [154221] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176740 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1362) 2,466 Black/admixed ancestry individuals NA Illumina [155125] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176741 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13633) 2,466 Black/admixed ancestry individuals NA Illumina [160229] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176742 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13633) 2,466 Black/admixed ancestry individuals NA Illumina [157902] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178762 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13644) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [167638] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176743 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13661) 2,466 Black/admixed ancestry individuals NA Illumina [154832] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176744 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1367) 2,466 Black/admixed ancestry individuals NA Illumina [152964] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176745 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI647) 2,466 Black/admixed ancestry individuals NA Illumina [151454] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178114 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6471) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158006] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178115 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI648) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153199] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178116 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6488) 2,466 Black/admixed ancestry individuals NA Illumina [165188] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178117 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6489) 2,466 Black/admixed ancestry individuals NA Illumina [154782] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178118 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI649) 2,466 Black/admixed ancestry individuals NA Illumina [148907] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178119 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6491) 2,466 Black/admixed ancestry individuals NA Illumina [149919] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178120 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6494) 2,466 Black/admixed ancestry individuals NA Illumina [149754] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178121 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6495) 2,466 Black/admixed ancestry individuals NA Illumina [150133] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178122 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6496) 2,466 Black/admixed ancestry individuals NA Illumina [149159] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178123 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6498) 2,466 Black/admixed ancestry individuals NA Illumina [160084] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178124 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI650) 2,466 Black/admixed ancestry individuals NA Illumina [170639] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178125 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6500) 2,466 Black/admixed ancestry individuals NA Illumina [150484] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178126 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6501) 2,466 Black/admixed ancestry individuals NA Illumina [150210] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178127 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6502) 2,466 Black/admixed ancestry individuals NA Illumina [151817] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178128 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6505) 2,466 Black/admixed ancestry individuals NA Illumina [158286] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178129 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6509) 2,466 Black/admixed ancestry individuals NA Illumina [168443] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178130 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI651) 2,466 Black/admixed ancestry individuals NA Illumina [152492] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178131 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12809) 2,466 Black/admixed ancestry individuals NA Illumina [156212] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176680 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12819) 2,466 Black/admixed ancestry individuals NA Illumina [153859] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176681 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12823) 2,466 Black/admixed ancestry individuals NA Illumina [172365] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178977 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12824) 2,466 Black/admixed ancestry individuals NA Illumina [171671] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176682 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12849) 2,466 Black/admixed ancestry individuals NA Illumina [151397] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176683 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12855) 2,466 Black/admixed ancestry individuals NA Illumina [154631] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176684 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12855) 2,466 Black/admixed ancestry individuals NA Illumina [157455] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178978 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12860) 2,466 Black/admixed ancestry individuals NA Illumina [151950] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176685 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12888) 2,466 Black/admixed ancestry individuals NA Illumina [138646] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176686 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1289) 2,466 Black/admixed ancestry individuals NA Illumina [155248] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176687 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1289) 2,466 Black/admixed ancestry individuals NA Illumina [148054] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178754 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12890) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158321] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176688 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12911) 2,466 Black/admixed ancestry individuals NA Illumina [147096] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176689 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12912) 2,466 Black/admixed ancestry individuals NA Illumina [146285] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176690 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12942) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157960] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176691 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12971) 2,466 Black/admixed ancestry individuals NA Illumina [150558] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176692 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12988) 2,466 Black/admixed ancestry individuals NA Illumina [151820] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176693 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13020) 2,466 Black/admixed ancestry individuals NA Illumina [180349] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176694 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13037) 2,466 Black/admixed ancestry individuals NA Illumina [150317] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176695 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13051) 2,466 Black/admixed ancestry individuals NA Illumina [157339] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176696 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13055) 2,466 Black/admixed ancestry individuals NA Illumina [159385] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178979 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13062) 2,466 Black/admixed ancestry individuals NA Illumina [143960] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176697 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13063) 2,466 Black/admixed ancestry individuals NA Illumina [152812] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176698 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13066) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153594] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176699 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13076) 2,466 Black/admixed ancestry individuals NA Illumina [153463] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176700 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13401) 2,466 Black/admixed ancestry individuals NA Illumina [152606] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176722 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13412) 2,466 Black/admixed ancestry individuals NA Illumina [149194] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176723 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13416) 2,466 Black/admixed ancestry individuals NA Illumina [155201] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176724 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13436) 2,466 Black/admixed ancestry individuals NA Illumina [154343] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176725 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13437) 2,466 Black/admixed ancestry individuals NA Illumina [151872] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176726 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13448) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150646] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176727 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13480) 2,466 Black/admixed ancestry individuals NA Illumina [192971] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178981 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1349) 2,466 Black/admixed ancestry individuals NA Illumina [157939] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176728 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13496) 2,466 Black/admixed ancestry individuals NA Illumina [164334] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176729 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13496) 2,466 Black/admixed ancestry individuals NA Illumina [166221] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178758 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13528) 2,466 Black/admixed ancestry individuals NA Illumina [161473] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178982 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13530) 2,466 Black/admixed ancestry individuals NA Illumina [171019] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176730 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13530) 2,466 Black/admixed ancestry individuals NA Illumina [159725] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178759 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1355) 2,466 Black/admixed ancestry individuals NA Illumina [153944] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176731 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1355) 2,466 Black/admixed ancestry individuals NA Illumina [156232] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178760 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13553) 2,466 Black/admixed ancestry individuals NA Illumina [149394] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176732 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13553) 2,466 Black/admixed ancestry individuals NA Illumina [150721] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178983 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13564) 2,466 Black/admixed ancestry individuals NA Illumina [161052] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176733 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1357) 2,466 Black/admixed ancestry individuals NA Illumina [155822] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176734 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13578) 2,466 Black/admixed ancestry individuals NA Illumina [154357] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176735 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13584) 2,466 Black/admixed ancestry individuals NA Illumina [151782] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176736 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13584) 2,466 Black/admixed ancestry individuals NA Illumina [146974] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178761 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13602) 2,466 Black/admixed ancestry individuals NA Illumina [154696] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176737 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13606) 2,466 Black/admixed ancestry individuals NA Illumina [154351] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176738 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13613) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157693] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176739 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6348) 2,466 Black/admixed ancestry individuals NA Illumina [149752] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178078 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI635) 2,466 Black/admixed ancestry individuals NA Illumina [150090] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178079 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6351) 2,466 Black/admixed ancestry individuals NA Illumina [152164] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178080 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6355) 2,466 Black/admixed ancestry individuals NA Illumina [156915] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178081 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6357) 2,466 Black/admixed ancestry individuals NA Illumina [151051] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178082 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6362) 2,466 Black/admixed ancestry individuals NA Illumina [170354] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178083 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6365) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154447] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178084 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6369) 2,466 Black/admixed ancestry individuals NA Illumina [159351] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178085 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6372) 2,466 Black/admixed ancestry individuals NA Illumina [152132] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178086 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6374) 2,466 Black/admixed ancestry individuals NA Illumina [155346] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178087 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6377) 2,466 Black/admixed ancestry individuals NA Illumina [149764] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178088 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6381) 2,466 Black/admixed ancestry individuals NA Illumina [147129] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178089 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6383) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155302] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178090 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6384) 2,466 Black/admixed ancestry individuals NA Illumina [150230] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178091 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6390) 2,466 Black/admixed ancestry individuals NA Illumina [155187] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178092 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6404) 2,466 Black/admixed ancestry individuals NA Illumina [146708] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178093 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6407) 2,466 Black/admixed ancestry individuals NA Illumina [148897] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178094 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6426) 2,466 Black/admixed ancestry individuals NA Illumina [155525] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178095 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI643) 2,466 Black/admixed ancestry individuals NA Illumina [156345] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178096 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6433) 2,466 Black/admixed ancestry individuals NA Illumina [173792] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178097 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6434) 2,466 Black/admixed ancestry individuals NA Illumina [169647] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178098 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6435) 2,466 Black/admixed ancestry individuals NA Illumina [158714] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178099 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6436) 2,466 Black/admixed ancestry individuals NA Illumina [174559] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178100 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6437) 2,466 Black/admixed ancestry individuals NA Illumina [137557] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178101 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6439) 2,466 Black/admixed ancestry individuals NA Illumina [171049] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178102 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7019) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159917] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178276 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7029) 2,466 Black/admixed ancestry individuals NA Illumina [156697] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178277 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI703) 2,466 Black/admixed ancestry individuals NA Illumina [156959] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178278 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7072) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157893] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178279 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7079) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163736] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178280 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7080) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [164263] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178281 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7082) 2,466 Black/admixed ancestry individuals NA Illumina [149091] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178282 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7085) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161438] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178283 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7086) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161453] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178284 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7089) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162200] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178285 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7090) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [176895] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178286 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7098) 2,466 Black/admixed ancestry individuals NA Illumina [143558] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178287 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI710) 2,466 Black/admixed ancestry individuals NA Illumina [154627] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178288 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7101) 2,466 Black/admixed ancestry individuals NA Illumina [165047] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178289 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7103) 2,466 Black/admixed ancestry individuals NA Illumina [151884] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178290 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7106) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156850] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178291 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7107) 2,466 Black/admixed ancestry individuals NA Illumina [160492] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178292 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7118) 2,466 Black/admixed ancestry individuals NA Illumina [169659] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178293 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI712) 2,466 Black/admixed ancestry individuals NA Illumina [166607] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178294 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14111) 2,466 Black/admixed ancestry individuals NA Illumina [150752] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176830 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14111) 2,466 Black/admixed ancestry individuals NA Illumina [151515] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178767 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14127) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155885] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176831 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14130) 2,466 Black/admixed ancestry individuals NA Illumina [148939] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176832 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14140) 2,466 Black/admixed ancestry individuals NA Illumina [150423] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176833 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14144) 2,466 Black/admixed ancestry individuals NA Illumina [156629] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176834 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6917) 2,466 Black/admixed ancestry individuals NA Illumina [162526] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178893 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI692) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155848] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178255 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6923) 2,466 Black/admixed ancestry individuals NA Illumina [149971] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178256 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6928) 2,466 Black/admixed ancestry individuals NA Illumina [152277] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178257 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6932) 2,466 Black/admixed ancestry individuals NA Illumina [165056] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178258 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6934) 2,466 Black/admixed ancestry individuals NA Illumina [165698] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178259 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6934) 2,466 Black/admixed ancestry individuals NA Illumina [150811] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179086 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI694) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161559] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178260 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI695) 2,466 Black/admixed ancestry individuals NA Illumina [152048] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178261 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6951) 2,466 Black/admixed ancestry individuals NA Illumina [186406] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178262 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6951) 2,466 Black/admixed ancestry individuals NA Illumina [187792] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178894 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6955) 2,466 Black/admixed ancestry individuals NA Illumina [162274] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178263 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI696) 2,466 Black/admixed ancestry individuals NA Illumina [166389] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178264 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6965) 2,466 Black/admixed ancestry individuals NA Illumina [152607] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178265 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6971) 2,466 Black/admixed ancestry individuals NA Illumina [150018] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178266 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6976) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158132] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178267 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI698) 2,466 Black/admixed ancestry individuals NA Illumina [131442] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178268 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6983) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155367] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178269 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6984) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157770] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178270 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6985) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158015] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178271 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI699) 2,466 Black/admixed ancestry individuals NA Illumina [153496] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178272 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6991) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161217] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178273 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI700) 2,466 Black/admixed ancestry individuals NA Illumina [166971] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178274 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI700) 2,466 Black/admixed ancestry individuals NA Illumina [164307] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178895 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7003) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153539] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178275 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1415) 2,466 Black/admixed ancestry individuals NA Illumina [164093] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176835 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1416) 2,466 Black/admixed ancestry individuals NA Illumina [145637] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176836 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1417) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157468] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176837 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14176) 2,466 Black/admixed ancestry individuals NA Illumina [166760] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176838 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1418) 2,466 Black/admixed ancestry individuals NA Illumina [151597] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176839 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14180) 2,466 Black/admixed ancestry individuals NA Illumina [217980] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178992 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14198) 2,466 Black/admixed ancestry individuals NA Illumina [214373] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178993 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14201) 2,466 Black/admixed ancestry individuals NA Illumina [147848] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176840 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14209) 2,466 Black/admixed ancestry individuals NA Illumina [164259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176841 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1421) 2,466 Black/admixed ancestry individuals NA Illumina [153642] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176842 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14216) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156076] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176843 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14244) 2,466 Black/admixed ancestry individuals NA Illumina [141924] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176844 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14244) 2,466 Black/admixed ancestry individuals NA Illumina [162112] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178768 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14245) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152961] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176845 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14263) 2,466 Black/admixed ancestry individuals NA Illumina [163459] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176846 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14275) 2,466 Black/admixed ancestry individuals NA Illumina [160774] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176847 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14277) 2,466 Black/admixed ancestry individuals NA Illumina [168035] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176848 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14282) 2,466 Black/admixed ancestry individuals NA Illumina [151655] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176849 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14283) 2,466 Black/admixed ancestry individuals NA Illumina [153703] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176850 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14288) 2,466 Black/admixed ancestry individuals NA Illumina [154220] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176851 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14289) 2,466 Black/admixed ancestry individuals NA Illumina [150376] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176852 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14294) 2,466 Black/admixed ancestry individuals NA Illumina [155579] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176853 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14295) 2,466 Black/admixed ancestry individuals NA Illumina [154416] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176854 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14296) 2,466 Black/admixed ancestry individuals NA Illumina [158979] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176855 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14297) 2,466 Black/admixed ancestry individuals NA Illumina [162445] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176856 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14108) 2,466 Black/admixed ancestry individuals NA Illumina [160553] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176828 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14109) 2,466 Black/admixed ancestry individuals NA Illumina [154664] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176829 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6750) 2,466 Black/admixed ancestry individuals NA Illumina [154642] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178210 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI676) 2,466 Black/admixed ancestry individuals NA Illumina [154602] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178211 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6762) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159117] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178212 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6770) 2,466 Black/admixed ancestry individuals NA Illumina [153572] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178213 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6777) 2,466 Black/admixed ancestry individuals NA Illumina [156648] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178214 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6778) 2,466 Black/admixed ancestry individuals NA Illumina [159750] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178215 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6778) 2,466 Black/admixed ancestry individuals NA Illumina [162058] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178890 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI678) 2,466 Black/admixed ancestry individuals NA Illumina [148453] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178216 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6780) 2,466 Black/admixed ancestry individuals NA Illumina [164129] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178217 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6785) 2,466 Black/admixed ancestry individuals NA Illumina [149457] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178218 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6785) 2,466 Black/admixed ancestry individuals NA Illumina [151228] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178891 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6788) 2,466 Black/admixed ancestry individuals NA Illumina [158123] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178219 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6789) 2,466 Black/admixed ancestry individuals NA Illumina [158062] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178220 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6795) 2,466 Black/admixed ancestry individuals NA Illumina [162860] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178221 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI68) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159277] 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178222 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI680) 2,466 Black/admixed ancestry individuals NA Illumina [153359] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178223 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6808) 2,466 Black/admixed ancestry individuals NA Illumina [156789] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178224 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6815) 2,466 Black/admixed ancestry individuals NA Illumina [166984] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178225 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6816) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152147] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178226 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI682) 2,466 Black/admixed ancestry individuals NA Illumina [150679] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178227 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6820) 2,466 Black/admixed ancestry individuals NA Illumina [152394] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178228 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6821) 2,466 Black/admixed ancestry individuals NA Illumina [153085] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178229 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6823) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151117] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178230 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6825) 2,466 Black/admixed ancestry individuals NA Illumina [160888] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178231 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6826) 2,466 Black/admixed ancestry individuals NA Illumina [161841] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178232 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6827) 2,466 Black/admixed ancestry individuals NA Illumina [164684] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178233 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6840) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [176107] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178234 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI685) 2,466 Black/admixed ancestry individuals NA Illumina [168700] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178235 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6854) 2,466 Black/admixed ancestry individuals NA Illumina [154484] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178236 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6854) 2,466 Black/admixed ancestry individuals NA Illumina [154104] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178892 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI686) 2,466 Black/admixed ancestry individuals NA Illumina [149376] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178237 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6867) 2,466 Black/admixed ancestry individuals NA Illumina [151966] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178238 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6871) 2,466 Black/admixed ancestry individuals NA Illumina [157154] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178239 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6879) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160279] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178240 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6882) 2,466 Black/admixed ancestry individuals NA Illumina [162544] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178241 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6887) 2,466 Black/admixed ancestry individuals NA Illumina [152276] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178242 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6891) 2,466 Black/admixed ancestry individuals NA Illumina [159408] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178243 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6892) 2,466 Black/admixed ancestry individuals NA Illumina [161505] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178244 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6896) 2,466 Black/admixed ancestry individuals NA Illumina [156464] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178245 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6901) 2,466 Black/admixed ancestry individuals NA Illumina [151149] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178246 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6902) 2,466 Black/admixed ancestry individuals NA Illumina [152751] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178247 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6903) 2,466 Black/admixed ancestry individuals NA Illumina [153025] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178248 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6904) 2,466 Black/admixed ancestry individuals NA Illumina [152461] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178249 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6905) 2,466 Black/admixed ancestry individuals NA Illumina [151312] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178250 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6906) 2,466 Black/admixed ancestry individuals NA Illumina [152493] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178251 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6907) 2,466 Black/admixed ancestry individuals NA Illumina [150851] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178252 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6914) 2,466 Black/admixed ancestry individuals NA Illumina [170600] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178253 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6917) 2,466 Black/admixed ancestry individuals NA Illumina [162392] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178254 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14298) 2,466 Black/admixed ancestry individuals NA Illumina [160226] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176857 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14299) 2,466 Black/admixed ancestry individuals NA Illumina [155629] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176858 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14300) 2,466 Black/admixed ancestry individuals NA Illumina [153616] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176859 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14301) 2,466 Black/admixed ancestry individuals NA Illumina [152175] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176860 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1431) 2,466 Black/admixed ancestry individuals NA Illumina [150244] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176861 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14316) 2,466 Black/admixed ancestry individuals NA Illumina [159900] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176862 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14329) 2,466 Black/admixed ancestry individuals NA Illumina [164266] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176863 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1433) 2,466 Black/admixed ancestry individuals NA Illumina [167914] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176864 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14354) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158726] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176865 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14357) 2,466 Black/admixed ancestry individuals NA Illumina [151520] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176866 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1436) 2,466 Black/admixed ancestry individuals NA Illumina [182527] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176867 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1436) 2,466 Black/admixed ancestry individuals NA Illumina [153970] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178769 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1437) 2,466 Black/admixed ancestry individuals NA Illumina [148176] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176868 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14383) 2,466 Black/admixed ancestry individuals NA Illumina [137905] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176869 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14420) 2,466 Black/admixed ancestry individuals NA Illumina [154419] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176870 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14421) 2,466 Black/admixed ancestry individuals NA Illumina [154347] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176871 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14425) 2,466 Black/admixed ancestry individuals NA Illumina [162982] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176872 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1443) 2,466 Black/admixed ancestry individuals NA Illumina [150795] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176873 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1444) 2,466 Black/admixed ancestry individuals NA Illumina [161864] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176874 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14455) 2,466 Black/admixed ancestry individuals NA Illumina [163506] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176875 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14455) 2,466 Black/admixed ancestry individuals NA Illumina [168865] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178770 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1446) 2,466 Black/admixed ancestry individuals NA Illumina [154232] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176876 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14476) 2,466 Black/admixed ancestry individuals NA Illumina [158207] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176877 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14484) 2,466 Black/admixed ancestry individuals NA Illumina [158871] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176878 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14484) 2,466 Black/admixed ancestry individuals NA Illumina [156655] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178994 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14487) 2,466 Black/admixed ancestry individuals NA Illumina [153163] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176879 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1449) 2,466 Black/admixed ancestry individuals NA Illumina [164184] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176880 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1449) 2,466 Black/admixed ancestry individuals NA Illumina [150044] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178771 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14490) 2,466 Black/admixed ancestry individuals NA Illumina [158051] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176881 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14492) 2,466 Black/admixed ancestry individuals NA Illumina [157575] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176882 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14492) 2,466 Black/admixed ancestry individuals NA Illumina [151601] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178772 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14494) 2,466 Black/admixed ancestry individuals NA Illumina [283929] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178995 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14497) 2,466 Black/admixed ancestry individuals NA Illumina [153930] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176883 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1451) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156114] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176884 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14511) 2,466 Black/admixed ancestry individuals NA Illumina [151577] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176885 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14515) 2,466 Black/admixed ancestry individuals NA Illumina [164152] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176886 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14515) 2,466 Black/admixed ancestry individuals NA Illumina [168975] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178773 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14517) 2,466 Black/admixed ancestry individuals NA Illumina [152000] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176887 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14517) 2,466 Black/admixed ancestry individuals NA Illumina [149134] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178774 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14522) 2,466 Black/admixed ancestry individuals NA Illumina [166018] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176888 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14523) 2,466 Black/admixed ancestry individuals NA Illumina [175544] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176889 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14523) 2,466 Black/admixed ancestry individuals NA Illumina [172054] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178775 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14525) 2,466 Black/admixed ancestry individuals NA Illumina [144368] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176890 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14526) 2,466 Black/admixed ancestry individuals NA Illumina [332429] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178996 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14527) 2,466 Black/admixed ancestry individuals NA Illumina [145788] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176891 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14547) 2,466 Black/admixed ancestry individuals NA Illumina [159587] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176892 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14547) 2,466 Black/admixed ancestry individuals NA Illumina [157620] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178776 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14549) 2,466 Black/admixed ancestry individuals NA Illumina [157616] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176893 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1455) 2,466 Black/admixed ancestry individuals NA Illumina [158802] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176894 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1455) 2,466 Black/admixed ancestry individuals NA Illumina [148655] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178777 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14854) 2,466 Black/admixed ancestry individuals NA Illumina [158725] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176984 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14855) 2,466 Black/admixed ancestry individuals NA Illumina [148472] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176985 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14863) 2,466 Black/admixed ancestry individuals NA Illumina [163839] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176986 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14863) 2,466 Black/admixed ancestry individuals NA Illumina [145874] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179002 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14865) 2,466 Black/admixed ancestry individuals NA Illumina [155200] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176987 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14865) 2,466 Black/admixed ancestry individuals NA Illumina [154473] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179003 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14866) 2,466 Black/admixed ancestry individuals NA Illumina [159191] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176988 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI806) 2,466 Black/admixed ancestry individuals NA Illumina [152204] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178377 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI807) 2,466 Black/admixed ancestry individuals NA Illumina [154043] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178378 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI810) 2,466 Black/admixed ancestry individuals NA Illumina [154802] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178379 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI815) 2,466 Black/admixed ancestry individuals NA Illumina [148040] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178380 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI82) 2,466 Black/admixed ancestry individuals NA Illumina [173210] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179091 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI830) 2,466 Black/admixed ancestry individuals NA Illumina [177422] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178381 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI830) 2,466 Black/admixed ancestry individuals NA Illumina [153674] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178904 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI839) 2,466 Black/admixed ancestry individuals NA Illumina [146763] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178382 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8421) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163348] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178383 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8422) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [178996] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178384 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI843) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159438] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178385 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI844) 2,466 Black/admixed ancestry individuals NA Illumina [168297] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178386 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8492) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [168893] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178387 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8540) 2,466 Black/admixed ancestry individuals NA Illumina [155304] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178388 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8556) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153832] 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178389 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8557) 2,466 Black/admixed ancestry individuals NA Illumina [156028] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178390 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8560) 2,466 Black/admixed ancestry individuals NA Illumina [163985] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178391 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI858) 2,466 Black/admixed ancestry individuals NA Illumina [149243] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178392 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14771) 2,466 Black/admixed ancestry individuals NA Illumina [154596] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178787 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14776) 2,466 Black/admixed ancestry individuals NA Illumina [161309] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176964 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14777) 2,466 Black/admixed ancestry individuals NA Illumina [153455] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176965 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14778) 2,466 Black/admixed ancestry individuals NA Illumina [143463] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176966 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1478) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [166139] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176967 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1479) 2,466 Black/admixed ancestry individuals NA Illumina [166124] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176968 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14793) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159296] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176969 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14796) 2,466 Black/admixed ancestry individuals NA Illumina [154083] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176970 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14796) 2,466 Black/admixed ancestry individuals NA Illumina [148873] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178788 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14798) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155419] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176971 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1480) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152729] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176972 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1481) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148083] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176973 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14814) 2,466 Black/admixed ancestry individuals NA Illumina [149385] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176974 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14815) 2,466 Black/admixed ancestry individuals NA Illumina [150274] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176975 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14816) 2,466 Black/admixed ancestry individuals NA Illumina [136977] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176976 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14818) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161181] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176977 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14825) 2,466 Black/admixed ancestry individuals NA Illumina [168031] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176978 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14825) 2,466 Black/admixed ancestry individuals NA Illumina [170479] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178789 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1483) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148010] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176979 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14832) 2,466 Black/admixed ancestry individuals NA Illumina [154012] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176980 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14846) 2,466 Black/admixed ancestry individuals NA Illumina [154865] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176981 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14846) 2,466 Black/admixed ancestry individuals NA Illumina [145931] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179000 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1485) 2,466 Black/admixed ancestry individuals NA Illumina [154457] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176982 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1485) 2,466 Black/admixed ancestry individuals NA Illumina [143008] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179001 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14853) 2,466 Black/admixed ancestry individuals NA Illumina [156706] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176983 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8930) 2,466 Black/admixed ancestry individuals NA Illumina [151637] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178909 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8931) 2,466 Black/admixed ancestry individuals NA Illumina [145629] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178437 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8941) 2,466 Black/admixed ancestry individuals NA Illumina [166333] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178438 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8944) 2,466 Black/admixed ancestry individuals NA Illumina [157100] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178439 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8944) 2,466 Black/admixed ancestry individuals NA Illumina [148076] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178910 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8946) 2,466 Black/admixed ancestry individuals NA Illumina [163851] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178440 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8948) 2,466 Black/admixed ancestry individuals NA Illumina [152204] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178441 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8963) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [164211] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178442 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8965) 2,466 Black/admixed ancestry individuals NA Illumina [168028] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178443 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8972) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [185923] 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178444 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8977) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158277] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178445 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8979) 2,466 Black/admixed ancestry individuals NA Illumina [161061] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178446 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8984) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158499] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178447 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI899) 2,466 Black/admixed ancestry individuals NA Illumina [153725] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178448 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8997) 2,466 Black/admixed ancestry individuals NA Illumina [162737] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178449 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9) 2,466 Black/admixed ancestry individuals NA Illumina [153234] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178450 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI900) 2,466 Black/admixed ancestry individuals NA Illumina [161882] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178451 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9038) 2,466 Black/admixed ancestry individuals NA Illumina [166654] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178452 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI904) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150627] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178453 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9050) 2,466 Black/admixed ancestry individuals NA Illumina [152110] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178454 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9055) 2,466 Black/admixed ancestry individuals NA Illumina [151310] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178455 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI906) 2,466 Black/admixed ancestry individuals NA Illumina [182534] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178456 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9071) 2,466 Black/admixed ancestry individuals NA Illumina [160694] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178457 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9072) 2,466 Black/admixed ancestry individuals NA Illumina [153790] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178458 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9090) 2,466 Black/admixed ancestry individuals NA Illumina [167340] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178459 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8787) 2,466 Black/admixed ancestry individuals NA Illumina [155100] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178416 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8792) 2,466 Black/admixed ancestry individuals NA Illumina [170678] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178417 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8793) 2,466 Black/admixed ancestry individuals NA Illumina [171773] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178418 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8798) 2,466 Black/admixed ancestry individuals NA Illumina [162000] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178419 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI881) 2,466 Black/admixed ancestry individuals NA Illumina [150725] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178420 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI881) 2,466 Black/admixed ancestry individuals NA Illumina [161502] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179092 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8810) 2,466 Black/admixed ancestry individuals NA Illumina [152016] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178421 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8814) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153354] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178422 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8826) 2,466 Black/admixed ancestry individuals NA Illumina [163347] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178423 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8826) 2,466 Black/admixed ancestry individuals NA Illumina [147778] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179093 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8853) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153475] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178424 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8855) 2,466 Black/admixed ancestry individuals NA Illumina [147613] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178425 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8856) 2,466 Black/admixed ancestry individuals NA Illumina [156931] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178426 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8858) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [170248] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178427 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8875) 2,466 Black/admixed ancestry individuals NA Illumina [156905] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178428 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8875) 2,466 Black/admixed ancestry individuals NA Illumina [156959] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178907 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI888) 2,466 Black/admixed ancestry individuals NA Illumina [147994] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178429 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8888) 2,466 Black/admixed ancestry individuals NA Illumina [157939] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178430 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI889) 2,466 Black/admixed ancestry individuals NA Illumina [161953] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178431 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8894) 2,466 Black/admixed ancestry individuals NA Illumina [174791] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178432 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI890) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152974] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178433 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8919) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155219] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178434 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8921) 2,466 Black/admixed ancestry individuals NA Illumina [148633] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178435 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8921) 2,466 Black/admixed ancestry individuals NA Illumina [155903] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178908 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8930) 2,466 Black/admixed ancestry individuals NA Illumina [155891] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178436 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14715) 2,466 Black/admixed ancestry individuals NA Illumina [147704] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176943 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14715) 2,466 Black/admixed ancestry individuals NA Illumina [151294] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178783 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14717) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149804] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176944 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14718) 2,466 Black/admixed ancestry individuals NA Illumina [152924] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176945 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14719) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154074] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176946 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14723) 2,466 Black/admixed ancestry individuals NA Illumina [151290] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176947 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14730) 2,466 Black/admixed ancestry individuals NA Illumina [163452] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176948 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14730) 2,466 Black/admixed ancestry individuals NA Illumina [153598] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178784 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14731) 2,466 Black/admixed ancestry individuals NA Illumina [151774] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176949 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14733) 2,466 Black/admixed ancestry individuals NA Illumina [170204] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176950 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14734) 2,466 Black/admixed ancestry individuals NA Illumina [163129] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176951 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14736) 2,466 Black/admixed ancestry individuals NA Illumina [152143] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176952 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14737) 2,466 Black/admixed ancestry individuals NA Illumina [154003] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176953 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14740) 2,466 Black/admixed ancestry individuals NA Illumina [155974] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176954 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14741) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151510] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176955 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14744) 2,466 Black/admixed ancestry individuals NA Illumina [149887] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176956 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14744) 2,466 Black/admixed ancestry individuals NA Illumina [153853] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178785 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14748) 2,466 Black/admixed ancestry individuals NA Illumina [147182] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176957 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14750) 2,466 Black/admixed ancestry individuals NA Illumina [148727] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176958 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14755) 2,466 Black/admixed ancestry individuals NA Illumina [158263] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176959 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14758) 2,466 Black/admixed ancestry individuals NA Illumina [158331] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176960 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14761) 2,466 Black/admixed ancestry individuals NA Illumina [148087] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176961 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14761) 2,466 Black/admixed ancestry individuals NA Illumina [152987] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178786 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14769) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151748] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176962 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14771) 2,466 Black/admixed ancestry individuals NA Illumina [151766] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176963 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8596) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153555] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178393 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8596) 2,466 Black/admixed ancestry individuals NA Illumina [153586] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178905 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI860) 2,466 Black/admixed ancestry individuals NA Illumina [153562] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178394 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8614) 2,466 Black/admixed ancestry individuals NA Illumina [151626] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178395 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8618) 2,466 Black/admixed ancestry individuals NA Illumina [159093] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178396 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI862) 2,466 Black/admixed ancestry individuals NA Illumina [159373] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178397 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8638) 2,466 Black/admixed ancestry individuals NA Illumina [157378] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178398 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8638) 2,466 Black/admixed ancestry individuals NA Illumina [165364] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178906 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8650) 2,466 Black/admixed ancestry individuals NA Illumina [154641] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178399 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8671) 2,466 Black/admixed ancestry individuals NA Illumina [152530] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178400 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8699) 2,466 Black/admixed ancestry individuals NA Illumina [152087] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178401 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8703) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162333] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178402 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8711) 2,466 Black/admixed ancestry individuals NA Illumina [153839] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178403 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8712) 2,466 Black/admixed ancestry individuals NA Illumina [153970] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178404 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8729) 2,466 Black/admixed ancestry individuals NA Illumina [149158] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178405 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8742) 2,466 Black/admixed ancestry individuals NA Illumina [162395] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178406 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8747) 2,466 Black/admixed ancestry individuals NA Illumina [154191] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178407 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8748) 2,466 Black/admixed ancestry individuals NA Illumina [151233] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178408 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8749) 2,466 Black/admixed ancestry individuals NA Illumina [153265] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178409 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8750) 2,466 Black/admixed ancestry individuals NA Illumina [152172] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178410 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8764) 2,466 Black/admixed ancestry individuals NA Illumina [152417] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178411 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8768) 2,466 Black/admixed ancestry individuals NA Illumina [153128] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178412 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8774) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151263] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178413 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8775) 2,466 Black/admixed ancestry individuals NA Illumina [152209] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178414 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8785) 2,466 Black/admixed ancestry individuals NA Illumina [151023] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178415 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9093) 2,466 Black/admixed ancestry individuals NA Illumina [154366] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178460 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9096) 2,466 Black/admixed ancestry individuals NA Illumina [141674] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178461 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14866) 2,466 Black/admixed ancestry individuals NA Illumina [153956] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178790 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14869) 2,466 Black/admixed ancestry individuals NA Illumina [149437] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176989 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14871) 2,466 Black/admixed ancestry individuals NA Illumina [153171] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176990 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1489) 2,466 Black/admixed ancestry individuals NA Illumina [151713] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176991 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14891) 2,466 Black/admixed ancestry individuals NA Illumina [176910] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176992 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14891) 2,466 Black/admixed ancestry individuals NA Illumina [154972] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178791 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14892) 2,466 Black/admixed ancestry individuals NA Illumina [147760] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176993 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14909) 2,466 Black/admixed ancestry individuals NA Illumina [145219] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176994 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14909) 2,466 Black/admixed ancestry individuals NA Illumina [152629] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178792 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14928) 2,466 Black/admixed ancestry individuals NA Illumina [154899] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176995 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14931) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154581] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176996 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14944) 2,466 Black/admixed ancestry individuals NA Illumina [148917] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176997 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14947) 2,466 Black/admixed ancestry individuals NA Illumina [173543] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176998 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14958) 2,466 Black/admixed ancestry individuals NA Illumina [144912] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176999 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14960) 2,466 Black/admixed ancestry individuals NA Illumina [158614] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177000 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14961) 2,466 Black/admixed ancestry individuals NA Illumina [155056] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177001 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14970) 2,466 Black/admixed ancestry individuals NA Illumina [132661] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177002 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14988) 2,466 Black/admixed ancestry individuals NA Illumina [149314] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177003 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14990) 2,466 Black/admixed ancestry individuals NA Illumina [154402] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177004 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14991) 2,466 Black/admixed ancestry individuals NA Illumina [156279] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177005 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14992) 2,466 Black/admixed ancestry individuals NA Illumina [157384] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177006 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14997) 2,466 Black/admixed ancestry individuals NA Illumina [149181] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177007 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14999) 2,466 Black/admixed ancestry individuals NA Illumina [160085] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177008 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15517) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160612] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177132 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15519) 2,466 Black/admixed ancestry individuals NA Illumina [151294] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177133 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15520) 2,466 Black/admixed ancestry individuals NA Illumina [155244] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177134 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15521) 2,466 Black/admixed ancestry individuals NA Illumina [155026] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177135 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15522) 2,466 Black/admixed ancestry individuals NA Illumina [156209] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177136 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1553) 2,466 Black/admixed ancestry individuals NA Illumina [152697] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177137 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15530) 2,466 Black/admixed ancestry individuals NA Illumina [162086] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177138 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15530) 2,466 Black/admixed ancestry individuals NA Illumina [151301] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178805 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15533) 2,466 Black/admixed ancestry individuals NA Illumina [149011] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177139 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15535) 2,466 Black/admixed ancestry individuals NA Illumina [154060] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177140 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15536) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154548] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177141 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15537) 2,466 Black/admixed ancestry individuals NA Illumina [152361] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177142 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15539) 2,466 Black/admixed ancestry individuals NA Illumina [156686] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177143 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15540) 2,466 Black/admixed ancestry individuals NA Illumina [151632] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177144 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15541) 2,466 Black/admixed ancestry individuals NA Illumina [153353] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177145 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15542) 2,466 Black/admixed ancestry individuals NA Illumina [156815] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177146 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15544) 2,466 Black/admixed ancestry individuals NA Illumina [150381] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177147 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15545) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157820] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177148 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15546) 2,466 Black/admixed ancestry individuals NA Illumina [155168] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177149 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15549) 2,466 Black/admixed ancestry individuals NA Illumina [154171] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177150 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15550) 2,466 Black/admixed ancestry individuals NA Illumina [153751] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177151 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15557) 2,466 Black/admixed ancestry individuals NA Illumina [151381] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177152 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15558) 2,466 Black/admixed ancestry individuals NA Illumina [156836] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177153 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15562) 2,466 Black/admixed ancestry individuals NA Illumina [153910] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177154 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15563) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [169272] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177155 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15437) 2,466 Black/admixed ancestry individuals NA Illumina [169524] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178803 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15450) 2,466 Black/admixed ancestry individuals NA Illumina [154608] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177110 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15454) 2,466 Black/admixed ancestry individuals NA Illumina [152264] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177111 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15457) 2,466 Black/admixed ancestry individuals NA Illumina [149774] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177112 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15458) 2,466 Black/admixed ancestry individuals NA Illumina [150956] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177113 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15459) 2,466 Black/admixed ancestry individuals NA Illumina [153476] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177114 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15464) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152819] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177115 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15464) 2,466 Black/admixed ancestry individuals NA Illumina [155296] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178804 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15469) 2,466 Black/admixed ancestry individuals NA Illumina [148991] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177116 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15470) 2,466 Black/admixed ancestry individuals NA Illumina [160135] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177117 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15472) 2,466 Black/admixed ancestry individuals NA Illumina [162897] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177118 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15473) 2,466 Black/admixed ancestry individuals NA Illumina [156750] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177119 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15484) 2,466 Black/admixed ancestry individuals NA Illumina [154601] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177120 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15488) 2,466 Black/admixed ancestry individuals NA Illumina [165408] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177121 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15493) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153424] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177122 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15498) 2,466 Black/admixed ancestry individuals NA Illumina [152624] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177123 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15501) 2,466 Black/admixed ancestry individuals NA Illumina [153607] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177124 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15502) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155794] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177125 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15503) 2,466 Black/admixed ancestry individuals NA Illumina [164215] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177126 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15504) 2,466 Black/admixed ancestry individuals NA Illumina [145768] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179012 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15505) 2,466 Black/admixed ancestry individuals NA Illumina [155766] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177127 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15512) 2,466 Black/admixed ancestry individuals NA Illumina [158935] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177128 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15513) 2,466 Black/admixed ancestry individuals NA Illumina [151590] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177129 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15514) 2,466 Black/admixed ancestry individuals NA Illumina [158186] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177130 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15516) 2,466 Black/admixed ancestry individuals NA Illumina [173399] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177131 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15348) 2,466 Black/admixed ancestry individuals NA Illumina [150902] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177089 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1535) 2,466 Black/admixed ancestry individuals NA Illumina [142807] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177090 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15350) 2,466 Black/admixed ancestry individuals NA Illumina [157565] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177091 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15350) 2,466 Black/admixed ancestry individuals NA Illumina [160313] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178799 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15366) 2,466 Black/admixed ancestry individuals NA Illumina [164211] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177092 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15369) 2,466 Black/admixed ancestry individuals NA Illumina [147319] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177093 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15372) 2,466 Black/admixed ancestry individuals NA Illumina [162003] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177094 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15372) 2,466 Black/admixed ancestry individuals NA Illumina [148664] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178800 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15375) 2,466 Black/admixed ancestry individuals NA Illumina [151206] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177095 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15377) 2,466 Black/admixed ancestry individuals NA Illumina [163751] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177096 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15381) 2,466 Black/admixed ancestry individuals NA Illumina [151983] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177097 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15385) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155303] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177098 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15385) 2,466 Black/admixed ancestry individuals NA Illumina [152631] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178801 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15388) 2,466 Black/admixed ancestry individuals NA Illumina [146720] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177099 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15390) 2,466 Black/admixed ancestry individuals NA Illumina [167701] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177100 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15399) 2,466 Black/admixed ancestry individuals NA Illumina [150166] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177101 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15399) 2,466 Black/admixed ancestry individuals NA Illumina [152708] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178802 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15402) 2,466 Black/admixed ancestry individuals NA Illumina [156935] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177102 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15403) 2,466 Black/admixed ancestry individuals NA Illumina [150914] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177103 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15404) 2,466 Black/admixed ancestry individuals NA Illumina [155556] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177104 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15422) 2,466 Black/admixed ancestry individuals NA Illumina [153778] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177105 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15432) 2,466 Black/admixed ancestry individuals NA Illumina [163272] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177106 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15434) 2,466 Black/admixed ancestry individuals NA Illumina [152564] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177107 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15436) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157219] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177108 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15437) 2,466 Black/admixed ancestry individuals NA Illumina [175868] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177109 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15567) 2,466 Black/admixed ancestry individuals NA Illumina [151908] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177156 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15568) 2,466 Black/admixed ancestry individuals NA Illumina [162323] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177157 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15571) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153595] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177158 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15572) 2,466 Black/admixed ancestry individuals NA Illumina [153258] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177159 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15573) 2,466 Black/admixed ancestry individuals NA Illumina [160332] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177160 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15574) 2,466 Black/admixed ancestry individuals NA Illumina [152448] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177161 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15575) 2,466 Black/admixed ancestry individuals NA Illumina [152301] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177162 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15576) 2,466 Black/admixed ancestry individuals NA Illumina [156214] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177163 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16006) 2,466 Black/admixed ancestry individuals NA Illumina [160435] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177344 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16015) 2,466 Black/admixed ancestry individuals NA Illumina [146607] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177345 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16015) 2,466 Black/admixed ancestry individuals NA Illumina [145819] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179018 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16024) 2,466 Black/admixed ancestry individuals NA Illumina [159106] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177346 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16027) 2,466 Black/admixed ancestry individuals NA Illumina [176682] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177347 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16027) 2,466 Black/admixed ancestry individuals NA Illumina [151856] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178819 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16030) 2,466 Black/admixed ancestry individuals NA Illumina [146710] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177348 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16036) 2,466 Black/admixed ancestry individuals NA Illumina [153305] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177349 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1604) 2,466 Black/admixed ancestry individuals NA Illumina [141351] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177350 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16063) 2,466 Black/admixed ancestry individuals NA Illumina [148844] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177351 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16069) 2,466 Black/admixed ancestry individuals NA Illumina [164470] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177352 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16069) 2,466 Black/admixed ancestry individuals NA Illumina [162608] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178820 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16079) 2,466 Black/admixed ancestry individuals NA Illumina [168068] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177353 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16079) 2,466 Black/admixed ancestry individuals NA Illumina [161026] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178821 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16124) 2,466 Black/admixed ancestry individuals NA Illumina [149778] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177354 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16131) 2,466 Black/admixed ancestry individuals NA Illumina [144875] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179019 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16149) 2,466 Black/admixed ancestry individuals NA Illumina [148508] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177355 Genome-wide sequencing 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. White blood cell count 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90134668 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Percent lymphocyte 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90134669 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Percent mononuclear cells 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90134670 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Percent neutrophils 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90134671 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Percent eosinophils 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90134672 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Percent basophils 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90134673 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Absolute monocyte count 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90134674 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Absolute neutrophil count 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90134675 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Absolute eosinophil count 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90134676 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Absolute basophil count 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90134677 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Platelet count 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90134678 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Platelet distribution width 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 platelet component distribution width http://www.ebi.ac.uk/efo/EFO_0007984 GCST90134679 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Mean platelet volume 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90134680 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Red blood cell count 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90134681 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Hemoglobin 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 1 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90134682 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Mean corpuscular volume 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90134683 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Mean corpuscular hemoglobin 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90134684 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Mean corpuscular hemoglobin concentration 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90134685 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Percent red cell distribution width 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 Red cell distribution width http://www.ebi.ac.uk/efo/EFO_0009188 GCST90134686 Genome-wide genotyping array 2022-09-20 35945964 Yang W 2022-08-03 Pharmgenomics Pers Med www.ncbi.nlm.nih.gov/pubmed/35945964 Genome-Wide Association Study on the Hematological Phenotypic Characteristics of the Han Population from Northwest China. Red cell distribution width 1,005 Han Chinese ancestry individuals 2,047 Han Chinese ancestry individuals Affymetrix [9336679] (imputed) 0 Red cell distribution width http://www.ebi.ac.uk/efo/EFO_0009188 GCST90134687 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1917) 2,466 Black/admixed ancestry individuals NA Illumina [159636] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177423 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI194) 2,466 Black/admixed ancestry individuals NA Illumina [156160] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177425 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1971) 2,466 Black/admixed ancestry individuals NA Illumina [162794] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177430 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9757) 2,466 Black/admixed ancestry individuals NA Illumina [161950] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178629 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI976) 2,466 Black/admixed ancestry individuals NA Illumina [154366] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178632 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9767) 2,466 Black/admixed ancestry individuals NA Illumina [157205] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179099 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI977) 2,466 Black/admixed ancestry individuals NA Illumina [140466] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178634 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9774) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148487] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178635 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9777) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153324] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178636 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9778) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155860] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178637 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9779) 2,466 Black/admixed ancestry individuals NA Illumina [155852] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178638 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9782) 2,466 Black/admixed ancestry individuals NA Illumina [143355] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178639 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9783) 2,466 Black/admixed ancestry individuals NA Illumina [152830] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178640 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9786) 2,466 Black/admixed ancestry individuals NA Illumina [156582] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178641 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9789) 2,466 Black/admixed ancestry individuals NA Illumina [153069] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178642 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9795) 2,466 Black/admixed ancestry individuals NA Illumina [136871] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178643 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9795) 2,466 Black/admixed ancestry individuals NA Illumina [145822] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178913 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9798) 2,466 Black/admixed ancestry individuals NA Illumina [151238] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178644 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9806) 2,466 Black/admixed ancestry individuals NA Illumina [153895] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178645 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9806) 2,466 Black/admixed ancestry individuals NA Illumina [149051] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178914 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9807) 2,466 Black/admixed ancestry individuals NA Illumina [148639] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178646 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9808) 2,466 Black/admixed ancestry individuals NA Illumina [148163] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178647 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9809) 2,466 Black/admixed ancestry individuals NA Illumina [145805] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178648 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9810) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150966] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178649 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9811) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150130] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178650 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI982) 2,466 Black/admixed ancestry individuals NA Illumina [155546] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178651 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9828) 2,466 Black/admixed ancestry individuals NA Illumina [150788] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178652 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9832) 2,466 Black/admixed ancestry individuals NA Illumina [152601] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178653 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9833) 2,466 Black/admixed ancestry individuals NA Illumina [151148] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178654 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9834) 2,466 Black/admixed ancestry individuals NA Illumina [153696] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178655 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9844) 2,466 Black/admixed ancestry individuals NA Illumina [157415] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178656 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9845) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155042] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178657 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9849) 2,466 Black/admixed ancestry individuals NA Illumina [152568] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178658 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9856) 2,466 Black/admixed ancestry individuals NA Illumina [151322] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178659 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9858) 2,466 Black/admixed ancestry individuals NA Illumina [166959] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178660 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9862) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156613] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178661 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9871) 2,466 Black/admixed ancestry individuals NA Illumina [148561] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178662 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI180) 2,466 Black/admixed ancestry individuals NA Illumina [154296] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177396 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1811) 2,466 Black/admixed ancestry individuals NA Illumina [162617] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177397 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1821) 2,466 Black/admixed ancestry individuals NA Illumina [146909] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177398 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1822) 2,466 Black/admixed ancestry individuals NA Illumina [145551] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177399 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1839) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160217] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177400 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI184) 2,466 Black/admixed ancestry individuals NA Illumina [147606] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177401 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1840) 2,466 Black/admixed ancestry individuals NA Illumina [156236] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177402 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1841) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159678] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177403 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1857) 2,466 Black/admixed ancestry individuals NA Illumina [141699] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177404 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI188) 2,466 Black/admixed ancestry individuals NA Illumina [161002] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177405 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1883) 2,466 Black/admixed ancestry individuals NA Illumina [150440] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177406 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1885) 2,466 Black/admixed ancestry individuals NA Illumina [145826] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177407 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1886) 2,466 Black/admixed ancestry individuals NA Illumina [147255] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177408 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1887) 2,466 Black/admixed ancestry individuals NA Illumina [139514] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177409 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI189) 2,466 Black/admixed ancestry individuals NA Illumina [160262] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177410 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI189) 2,466 Black/admixed ancestry individuals NA Illumina [162923] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178829 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1890) 2,466 Black/admixed ancestry individuals NA Illumina [142655] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177411 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1893) 2,466 Black/admixed ancestry individuals NA Illumina [156152] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177412 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1894) 2,466 Black/admixed ancestry individuals NA Illumina [157135] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177413 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1895) 2,466 Black/admixed ancestry individuals NA Illumina [158630] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177414 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1896) 2,466 Black/admixed ancestry individuals NA Illumina [149593] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177415 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1897) 2,466 Black/admixed ancestry individuals NA Illumina [166312] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177416 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1898) 2,466 Black/admixed ancestry individuals NA Illumina [160019] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177417 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1899) 2,466 Black/admixed ancestry individuals NA Illumina [158363] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177418 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI190) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153521] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177419 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15763) 2,466 Black/admixed ancestry individuals NA Illumina [152444] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177243 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15764) 2,466 Black/admixed ancestry individuals NA Illumina [175264] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177244 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15766) 2,466 Black/admixed ancestry individuals NA Illumina [157983] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177245 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15767) 2,466 Black/admixed ancestry individuals NA Illumina [152080] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177246 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15768) 2,466 Black/admixed ancestry individuals NA Illumina [151816] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177247 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15770) 2,466 Black/admixed ancestry individuals NA Illumina [156537] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177248 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15771) 2,466 Black/admixed ancestry individuals NA Illumina [158221] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177249 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15775) 2,466 Black/admixed ancestry individuals NA Illumina [153187] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177250 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15779) 2,466 Black/admixed ancestry individuals NA Illumina [151298] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177251 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1578) 2,466 Black/admixed ancestry individuals NA Illumina [141430] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177252 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15780) 2,466 Black/admixed ancestry individuals NA Illumina [135865] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177253 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15781) 2,466 Black/admixed ancestry individuals NA Illumina [154512] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177254 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15782) 2,466 Black/admixed ancestry individuals NA Illumina [154553] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177255 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15783) 2,466 Black/admixed ancestry individuals NA Illumina [151665] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177256 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15784) 2,466 Black/admixed ancestry individuals NA Illumina [156841] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177257 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15785) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159340] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177258 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15786) 2,466 Black/admixed ancestry individuals NA Illumina [157003] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177259 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1719) 2,466 Black/admixed ancestry individuals NA Illumina [155497] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177390 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1723) 2,466 Black/admixed ancestry individuals NA Illumina [164749] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177391 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1723) 2,466 Black/admixed ancestry individuals NA Illumina [167575] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178828 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1727) 2,466 Black/admixed ancestry individuals NA Illumina [154134] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177392 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI175) 2,466 Black/admixed ancestry individuals NA Illumina [158255] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177393 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI175) 2,466 Black/admixed ancestry individuals NA Illumina [143069] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179032 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1783) 2,466 Black/admixed ancestry individuals NA Illumina [164096] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177394 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI179) 2,466 Black/admixed ancestry individuals NA Illumina [153055] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177395 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1902) 2,466 Black/admixed ancestry individuals NA Illumina [156877] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177420 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1905) 2,466 Black/admixed ancestry individuals NA Illumina [159423] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177421 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1915) 2,466 Black/admixed ancestry individuals NA Illumina [152398] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177422 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI193) 2,466 Black/admixed ancestry individuals NA Illumina [156931] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177424 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1942) 2,466 Black/admixed ancestry individuals NA Illumina [151967] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177426 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1942) 2,466 Black/admixed ancestry individuals NA Illumina [147817] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178830 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI195) 2,466 Black/admixed ancestry individuals NA Illumina [157009] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177427 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1965) 2,466 Black/admixed ancestry individuals NA Illumina [148440] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177428 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI197) 2,466 Black/admixed ancestry individuals NA Illumina [153385] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177429 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9754) 2,466 Black/admixed ancestry individuals NA Illumina [168082] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178628 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9758) 2,466 Black/admixed ancestry individuals NA Illumina [152831] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178630 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9759) 2,466 Black/admixed ancestry individuals NA Illumina [173233] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178631 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9760) 2,466 Black/admixed ancestry individuals NA Illumina [164773] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178633 Genome-wide sequencing 2022-09-14 35922517 COVID-19 Host Genetics Initiative 2022-08-03 Nature www.ncbi.nlm.nih.gov/pubmed/35922517 A first update on mapping the human genetic architecture of COVID-19. COVID-19 (critical illness vs population) 188 African ancestry cases, 11,232 African ancestry controls, 641 Hispanic or Latin American cases, 95,479 Hispanic or Latin American controls, 441 East Asian ancestry cases, 2,776 East Asian ancestry controls, 7,641 European ancestry cases, 1,632,197 European ancestry controls, 314 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 948 Greater Middle Eastern (Middle Eastern, North African or Persian) controls, 151 South Asian ancestry cases, 34,013 South Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90134596 Genome-wide genotyping array 2022-09-14 35922517 COVID-19 Host Genetics Initiative 2022-08-03 Nature www.ncbi.nlm.nih.gov/pubmed/35922517 A first update on mapping the human genetic architecture of COVID-19. COVID-19 (hospitalized vs population) 2,113 African ancestry cases, 121,925 African ancestry controls, 1,709 Hispanic or Latin American cases, 150,547 Hispanic or Latin American controls, 1,551 East Asian ancestry cases, 15,825 East Asian ancestry controls, 18,605 European ancestry cases, 2,490,909 European ancestry controls, 584 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 14,491 Greater Middle Eastern (Middle Eastern, North African or Persian) controls, 465 South Asian ancestry cases, 42,575 South Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90134597 Genome-wide genotyping array 2022-09-14 35922517 COVID-19 Host Genetics Initiative 2022-08-03 Nature www.ncbi.nlm.nih.gov/pubmed/35922517 A first update on mapping the human genetic architecture of COVID-19. SARS-CoV-2 infection 8,461 African ancestry cases, 127,310 African ancestry controls, 10,109 Hispanic or Latin American cases, 75,831 Hispanic or Latin American controls, 2,047 East Asian ancestry cases, 19,113 East Asian ancestry controls, 97,783 European ancestry cases, 2,295,876 European ancestry controls, 1,103 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 15,818 Greater Middle Eastern (Middle Eastern, North African or Persian) controls, 6,081 South Asian ancestry cases, 41,399 South Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 14 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90134598 Genome-wide genotyping array 2022-09-14 35922517 COVID-19 Host Genetics Initiative 2022-08-03 Nature www.ncbi.nlm.nih.gov/pubmed/35922517 A first update on mapping the human genetic architecture of COVID-19. COVID-19 (critical illness vs population) 188 African ancestry cases, 11,232 African ancestry controls, 539 Hispanic or Latin American cases, 1,149 Hispanic or Latin American controls, 441 East Asian ancestry cases, 2,776 East Asian ancestry controls, 7,146 European ancestry cases, 951,757 European ancestry controls, 314 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 948 Greater Middle Eastern (Middle Eastern, North African or Persian) controls, 151 South Asian ancestry cases, 34,013 South Asian ancestry controls NA Affymetrix, Illumina [8141177] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90134599 Genome-wide genotyping array 2022-09-14 35922517 COVID-19 Host Genetics Initiative 2022-08-03 Nature www.ncbi.nlm.nih.gov/pubmed/35922517 A first update on mapping the human genetic architecture of COVID-19. COVID-19 (hospitalized vs population) 2,113 African ancestry cases, 121,925 African ancestry controls, 1,569 Hispanic or Latin American cases, 56,220 Hispanic or Latin American controls, 1,551 East Asian ancestry cases, 15,825 East Asian ancestry controls, 17,992 European ancestry cases, 1,810,493 European ancestry controls, 584 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 14,491 Greater Middle Eastern (Middle Eastern, North African or Persian) controls, 465 South Asian ancestry cases, 42,575 South Asian ancestry controls NA Affymetrix, Illumina [11811540] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90134600 Genome-wide genotyping array 2022-09-14 35922517 COVID-19 Host Genetics Initiative 2022-08-03 Nature www.ncbi.nlm.nih.gov/pubmed/35922517 A first update on mapping the human genetic architecture of COVID-19. SARS-CoV-2 infection 7,955 African ancestry cases, 124,200 African ancestry controls, 7,556 Hispanic or Latin American cases, 62,745 Hispanic or Latin American controls, 2,047 East Asian ancestry cases, 19,113 East Asian ancestry controls, 87,870 European ancestry cases, 2,210,804 European ancestry controls, 1,103 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 15,818 Greater Middle Eastern (Middle Eastern, North African or Persian) controls, 6,081 South Asian ancestry cases, 41,399 South Asian ancestry controls NA Affymetrix, Illumina [12223592] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90134601 Genome-wide genotyping array 2022-09-14 35922517 COVID-19 Host Genetics Initiative 2022-08-03 Nature www.ncbi.nlm.nih.gov/pubmed/35922517 A first update on mapping the human genetic architecture of COVID-19. COVID-19 (hospitalized vs not hospitalized) 1,749 African ancestry cases, 5,870 African ancestry controls, 716 Hispanic or Latin American cases, 5,515 Hispanic or Latin American controls, 11,280 European ancestry cases, 55,682 European ancestry controls, 270 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 823 Greater Middle Eastern (Middle Eastern, North African or Persian) controls, 465 South Asian ancestry cases, 5,301 South Asian ancestry controls NA Affymetrix, Illumina [13498844] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90134602 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9950) 2,466 Black/admixed ancestry individuals NA Illumina [141153] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179102 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9953) 2,466 Black/admixed ancestry individuals NA Illumina [148116] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178686 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9963) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161205] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178687 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9989) 2,466 Black/admixed ancestry individuals NA Illumina [162824] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178688 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9989) 2,466 Black/admixed ancestry individuals NA Illumina [155858] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178915 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9993) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156860] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178689 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9994) 2,466 Black/admixed ancestry individuals NA Illumina [152033] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178690 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9998) 2,466 Black/admixed ancestry individuals NA Illumina [163440] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178691 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QIna_MP1921) 2,466 Black/admixed ancestry individuals NA Illumina [173706] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177022 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QIna_MP2946) 2,466 Black/admixed ancestry individuals NA Illumina [173836] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178022 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Quinine levels 2,466 Black/admixed ancestry individuals NA Illumina [164743] 0 quinine measurement http://www.ebi.ac.uk/efo/EFO_0801218 GCST90179103 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Quinolinic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [152340] 0 quinolinic acid measurement http://www.ebi.ac.uk/efo/EFO_0010528 GCST90176073 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Ribothymidine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155533] 1 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90178692 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. S-adenosyl-L-homocysteine levels 2,466 Black/admixed ancestry individuals NA Illumina [155020] 0 S-(5-Adenosy)-L-homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0021666 GCST90176074 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Salicylic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [162827] 0 salicylic acid measurement http://www.ebi.ac.uk/efo/EFO_0020948 GCST90176127 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1579) 2,466 Black/admixed ancestry individuals NA Illumina [173066] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177260 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15791) 2,466 Black/admixed ancestry individuals NA Illumina [144047] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177261 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15794) 2,466 Black/admixed ancestry individuals NA Illumina [156734] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177262 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15795) 2,466 Black/admixed ancestry individuals NA Illumina [157575] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177263 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15796) 2,466 Black/admixed ancestry individuals NA Illumina [155197] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177264 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15798) 2,466 Black/admixed ancestry individuals NA Illumina [157199] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177265 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15799) 2,466 Black/admixed ancestry individuals NA Illumina [159578] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177266 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1580) 2,466 Black/admixed ancestry individuals NA Illumina [153589] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177267 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15800) 2,466 Black/admixed ancestry individuals NA Illumina [150177] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177268 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15801) 2,466 Black/admixed ancestry individuals NA Illumina [154880] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177269 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15925) 2,466 Black/admixed ancestry individuals NA Illumina [162898] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178809 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15928) 2,466 Black/admixed ancestry individuals NA Illumina [155402] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177317 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1593) 2,466 Black/admixed ancestry individuals NA Illumina [153652] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177318 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1593) 2,466 Black/admixed ancestry individuals NA Illumina [149519] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178810 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15931) 2,466 Black/admixed ancestry individuals NA Illumina [155161] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177319 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15931) 2,466 Black/admixed ancestry individuals NA Illumina [155936] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178811 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15932) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160984] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177320 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15940) 2,466 Black/admixed ancestry individuals NA Illumina [154254] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177321 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15940) 2,466 Black/admixed ancestry individuals NA Illumina [156635] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178812 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15944) 2,466 Black/admixed ancestry individuals NA Illumina [156550] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177322 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15944) 2,466 Black/admixed ancestry individuals NA Illumina [159772] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178813 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15945) 2,466 Black/admixed ancestry individuals NA Illumina [154399] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177323 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15945) 2,466 Black/admixed ancestry individuals NA Illumina [167097] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178814 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15951) 2,466 Black/admixed ancestry individuals NA Illumina [152526] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177324 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15951) 2,466 Black/admixed ancestry individuals NA Illumina [142076] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179016 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15952) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156485] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177325 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15953) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149021] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177326 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15955) 2,466 Black/admixed ancestry individuals NA Illumina [162725] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177327 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15955) 2,466 Black/admixed ancestry individuals NA Illumina [160045] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178815 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15960) 2,466 Black/admixed ancestry individuals NA Illumina [163305] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177328 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15961) 2,466 Black/admixed ancestry individuals NA Illumina [163586] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177329 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15961) 2,466 Black/admixed ancestry individuals NA Illumina [152146] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178816 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15962) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153967] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177330 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15965) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155771] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177331 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15966) 2,466 Black/admixed ancestry individuals NA Illumina [155851] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177332 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9873) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152069] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178663 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9878) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151077] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178664 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9880) 2,466 Black/admixed ancestry individuals NA Illumina [150546] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178665 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9882) 2,466 Black/admixed ancestry individuals NA Illumina [153467] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178666 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9885) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153807] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178667 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9886) 2,466 Black/admixed ancestry individuals NA Illumina [180628] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178668 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9886) 2,466 Black/admixed ancestry individuals NA Illumina [140044] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179100 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9888) 2,466 Black/admixed ancestry individuals NA Illumina [152550] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178669 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI989) 2,466 Black/admixed ancestry individuals NA Illumina [160817] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178670 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI989) 2,466 Black/admixed ancestry individuals NA Illumina [140702] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179101 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9892) 2,466 Black/admixed ancestry individuals NA Illumina [154399] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178671 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9896) 2,466 Black/admixed ancestry individuals NA Illumina [154944] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178672 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9897) 2,466 Black/admixed ancestry individuals NA Illumina [150448] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178673 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9900) 2,466 Black/admixed ancestry individuals NA Illumina [162494] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178674 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9905) 2,466 Black/admixed ancestry individuals NA Illumina [154642] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178675 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9907) 2,466 Black/admixed ancestry individuals NA Illumina [149972] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178676 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9912) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152111] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178677 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9913) 2,466 Black/admixed ancestry individuals NA Illumina [146661] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178678 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9917) 2,466 Black/admixed ancestry individuals NA Illumina [148661] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178679 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9920) 2,466 Black/admixed ancestry individuals NA Illumina [141964] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178680 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9936) 2,466 Black/admixed ancestry individuals NA Illumina [167932] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178681 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9938) 2,466 Black/admixed ancestry individuals NA Illumina [145250] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178682 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9947) 2,466 Black/admixed ancestry individuals NA Illumina [143690] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178683 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI995) 2,466 Black/admixed ancestry individuals NA Illumina [157870] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178684 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9950) 2,466 Black/admixed ancestry individuals NA Illumina [149596] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178685 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15802) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161926] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177270 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15803) 2,466 Black/admixed ancestry individuals NA Illumina [153020] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177271 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15804) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150996] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177272 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15805) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152961] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177273 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1581) 2,466 Black/admixed ancestry individuals NA Illumina [153094] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177274 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15814) 2,466 Black/admixed ancestry individuals NA Illumina [156028] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177275 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15816) 2,466 Black/admixed ancestry individuals NA Illumina [157185] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177276 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15817) 2,466 Black/admixed ancestry individuals NA Illumina [156541] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177277 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15818) 2,466 Black/admixed ancestry individuals NA Illumina [157108] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177278 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15820) 2,466 Black/admixed ancestry individuals NA Illumina [156732] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177279 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15821) 2,466 Black/admixed ancestry individuals NA Illumina [153582] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177280 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15822) 2,466 Black/admixed ancestry individuals NA Illumina [155510] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177281 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15823) 2,466 Black/admixed ancestry individuals NA Illumina [155212] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177282 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15827) 2,466 Black/admixed ancestry individuals NA Illumina [158580] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177283 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15829) 2,466 Black/admixed ancestry individuals NA Illumina [153851] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177284 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15831) 2,466 Black/admixed ancestry individuals NA Illumina [156544] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177285 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15832) 2,466 Black/admixed ancestry individuals NA Illumina [155826] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177286 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15842) 2,466 Black/admixed ancestry individuals NA Illumina [159668] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177287 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15843) 2,466 Black/admixed ancestry individuals NA Illumina [156496] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177288 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15844) 2,466 Black/admixed ancestry individuals NA Illumina [152496] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177289 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15845) 2,466 Black/admixed ancestry individuals NA Illumina [154797] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177290 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15846) 2,466 Black/admixed ancestry individuals NA Illumina [161995] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177291 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1585) 2,466 Black/admixed ancestry individuals NA Illumina [151994] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177292 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15850) 2,466 Black/admixed ancestry individuals NA Illumina [157809] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177293 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15850) 2,466 Black/admixed ancestry individuals NA Illumina [155990] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178808 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15972) 2,466 Black/admixed ancestry individuals NA Illumina [152010] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177333 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15973) 2,466 Black/admixed ancestry individuals NA Illumina [149227] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177334 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15975) 2,466 Black/admixed ancestry individuals NA Illumina [151761] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177335 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15979) 2,466 Black/admixed ancestry individuals NA Illumina [154369] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177336 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15979) 2,466 Black/admixed ancestry individuals NA Illumina [156463] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179017 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15981) 2,466 Black/admixed ancestry individuals NA Illumina [147717] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177337 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15981) 2,466 Black/admixed ancestry individuals NA Illumina [143678] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178817 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15983) 2,466 Black/admixed ancestry individuals NA Illumina [153428] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177338 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15993) 2,466 Black/admixed ancestry individuals NA Illumina [149868] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177339 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15995) 2,466 Black/admixed ancestry individuals NA Illumina [144322] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177340 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15998) 2,466 Black/admixed ancestry individuals NA Illumina [160301] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177341 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15998) 2,466 Black/admixed ancestry individuals NA Illumina [157208] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178818 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16) 2,466 Black/admixed ancestry individuals NA Illumina [157415] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177342 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16000) 2,466 Black/admixed ancestry individuals NA Illumina [156536] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177343 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1974) 2,466 Black/admixed ancestry individuals NA Illumina [140254] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177431 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI198) 2,466 Black/admixed ancestry individuals NA Illumina [162216] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177432 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI198) 2,466 Black/admixed ancestry individuals NA Illumina [150928] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178831 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1985) 2,466 Black/admixed ancestry individuals NA Illumina [333743] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179033 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI199) 2,466 Black/admixed ancestry individuals NA Illumina [163391] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177433 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1994) 2,466 Black/admixed ancestry individuals NA Illumina [162957] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177434 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2) 2,466 Black/admixed ancestry individuals NA Illumina [161523] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177435 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI200) 2,466 Black/admixed ancestry individuals NA Illumina [160671] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177436 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI2008) 2,466 Black/admixed ancestry individuals NA Illumina [149319] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177437 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI201) 2,466 Black/admixed ancestry individuals NA Illumina [149233] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177438 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI203) 2,466 Black/admixed ancestry individuals NA Illumina [152643] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177439 Genome-wide sequencing 2022-08-23 35671649 Cui J 2022-05-28 Semin Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/35671649 Genetics are not likely to offer clinically useful predictions for elevated liver enzyme levels in patients using low dose methotrexate. Alanine aminotransferase levels in low dose methotrexate treatment 1,429 European ancestry individuals NA Illumina [8800000] (imputed) 6 response to methotrexate, serum alanine aminotransferase measurement http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004735 GCST90132619 Genome-wide genotyping array 2022-08-23 35671649 Cui J 2022-05-28 Semin Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/35671649 Genetics are not likely to offer clinically useful predictions for elevated liver enzyme levels in patients using low dose methotrexate. Aspartate aminotransferase levels in low dose methotrexate treatment 1,429 European ancestry individuals NA Illumina [8800000] (imputed) 9 response to methotrexate, aspartate aminotransferase measurement http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004736 GCST90132620 Genome-wide genotyping array 2022-08-23 35671649 Cui J 2022-05-28 Semin Arthritis Rheum www.ncbi.nlm.nih.gov/pubmed/35671649 Genetics are not likely to offer clinically useful predictions for elevated liver enzyme levels in patients using low dose methotrexate. High aspartate aminotransferase or alanine aminotransferase levels in low dose methotrexate treatment 129 European ancestry cases, 1,300 European ancestry controls NA Illumina [8800000] (imputed) 3 response to methotrexate, aspartate aminotransferase measurement, serum alanine aminotransferase measurement http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004736, http://www.ebi.ac.uk/efo/EFO_0004735 GCST90132621 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 327; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015840 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 328; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015841 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 329; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015842 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 330; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015843 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 331; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015844 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 332; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015845 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 333; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015846 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 334; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015847 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 335; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015848 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 336; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015849 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 337; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015850 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 338; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015851 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 339; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015852 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 340; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015853 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 341; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015854 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 342; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015855 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 343; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015856 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 344; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015857 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 345; Facial segment 8; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015858 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 346; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015859 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 347; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015860 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 348; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015861 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 349; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015862 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 350; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015863 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 351; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015864 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 377; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015890 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 378; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015891 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 379; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015892 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 380; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015893 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 381; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015894 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 382; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015895 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 383; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015896 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 384; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015897 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 385; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015898 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 386; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015899 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 387; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015900 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 388; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015901 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 389; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015902 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 390; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015903 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 391; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015904 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 392; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015905 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 393; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015906 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 394; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015907 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 395; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015908 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 396; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015909 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 397; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015910 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 398; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015911 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 399; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015912 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 400; Facial segment 11; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015913 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 401; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015914 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 427; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015940 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 428; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015941 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 429; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015942 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 430; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015943 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 431; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015944 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 432; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015945 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 433; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015946 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 434; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015947 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 435; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015948 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 436; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015949 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 437; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015950 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 438; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015951 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 439; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015952 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 440; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015953 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 441; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015954 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 442; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015955 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 443; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015956 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 444; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015957 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 445; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015958 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 446; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015959 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 447; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015960 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 448; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015961 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 449; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015962 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 450; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015963 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 451; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015964 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 452; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015965 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 453; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015966 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 454; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015967 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 455; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015968 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 456; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015969 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 457; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015970 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 458; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015971 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 459; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015972 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 460; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015973 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 461; Facial segment 14; 3D morphology of the forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015974 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 462; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015975 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 463; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015976 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 464; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015977 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 465; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015978 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 466; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015979 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 467; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015980 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 468; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015981 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 469; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015982 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 470; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015983 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 471; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015984 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 472; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015985 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 473; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015986 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 474; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015987 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 475; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015988 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 476; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015989 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 402; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015915 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 403; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015916 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 404; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015917 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 405; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015918 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 406; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015919 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 407; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015920 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 408; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015921 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 409; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015922 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 410; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015923 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 411; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015924 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 412; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015925 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 413; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015926 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 414; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015927 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 415; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015928 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 416; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015929 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 417; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015930 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 418; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015931 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 419; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015932 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 420; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015933 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 421; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015934 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 422; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015935 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 423; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015936 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 424; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015937 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 425; Facial segment 12; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015938 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 426; Facial segment 13; 3D morphology of the chin and jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015939 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 302; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015815 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 303; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015816 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 304; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015817 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 305; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015818 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 306; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015819 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 307; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015820 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 308; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015821 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 309; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015822 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 310; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015823 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 311; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015824 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 312; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015825 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 313; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015826 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 314; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015827 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 315; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015828 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 316; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015829 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 317; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015830 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 318; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015831 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 319; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015832 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 320; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015833 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 321; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015834 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 322; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015835 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 323; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015836 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 324; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015837 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 325; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015838 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 326; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015839 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 352; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015865 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 353; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015866 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 354; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015867 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 355; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015868 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 356; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015869 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 357; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015870 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 358; Facial segment 9; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015871 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 359; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015872 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 360; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015873 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 361; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015874 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 362; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015875 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 363; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015876 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 364; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015877 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 365; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015878 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 366; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015879 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 367; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015880 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 368; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015881 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 369; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015882 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 370; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015883 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 371; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015884 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 372; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015885 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 373; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015886 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 374; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015887 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 375; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015888 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 376; Facial segment 10; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015889 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 477; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015990 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 478; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015991 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 479; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015992 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 480; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015993 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 481; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015994 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 482; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015995 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 483; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015996 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 484; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015997 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 485; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015998 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 486; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015999 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 487; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016000 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 488; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016001 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 489; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016002 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 490; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016003 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 491; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016004 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 492; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016005 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 493; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016006 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 494; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016007 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 495; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016008 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 496; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016009 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 497; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016010 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 498; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016011 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 499; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016012 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 500; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016013 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 501; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016014 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 527; Facial segment 18; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016040 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 528; Facial segment 18; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016041 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 529; Facial segment 18; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016042 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 530; Facial segment 18; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016043 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 531; Facial segment 19; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016044 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 532; Facial segment 19; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016045 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 533; Facial segment 19; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016046 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 534; Facial segment 19; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016047 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 535; Facial segment 20; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016048 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 536; Facial segment 20; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016049 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 537; Facial segment 20; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016050 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 538; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016051 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 539; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016052 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 540; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016053 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 541; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016054 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 542; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016055 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 543; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016056 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 544; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016057 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 545; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016058 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 546; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016059 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 547; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016060 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 548; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016061 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 549; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016062 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 550; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016063 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 551; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016064 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 502; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016015 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 503; Facial segment 15; 3D morphology of the eyes and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016016 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 504; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016017 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 505; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016018 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 506; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016019 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 507; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016020 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 508; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016021 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 509; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016022 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 510; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016023 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 511; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016024 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 512; Facial segment 16; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016025 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 513; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016026 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 514; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016027 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 515; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016028 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 516; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016029 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 517; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016030 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 518; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016031 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 519; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016032 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 520; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016033 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 521; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016034 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 522; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016035 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 523; Facial segment 17; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016036 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 524; Facial segment 18; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016037 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 525; Facial segment 18; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016038 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 526; Facial segment 18; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016039 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 552; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016065 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 553; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016066 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 554; Facial segment 21; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016067 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 555; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016068 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 556; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016069 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 557; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016070 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 558; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016071 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 559; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016072 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 560; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016073 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 561; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016074 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 562; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016075 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 563; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016076 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 564; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016077 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 565; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016078 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 566; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016079 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 567; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016080 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 568; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016081 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 569; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016082 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 570; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016083 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 571; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016084 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 572; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016085 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 573; Facial segment 22; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016086 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 574; Facial segment 23; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016087 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 575; Facial segment 23; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016088 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 576; Facial segment 23; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016089 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 577; Facial segment 23; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016090 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 578; Facial segment 23; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016091 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 579; Facial segment 23; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016092 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 580; Facial segment 23; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016093 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 581; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016094 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 582; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016095 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 583; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016096 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 584; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016097 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 585; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016098 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 586; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016099 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 587; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016100 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 588; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016101 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 589; Facial segment 24; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016102 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 590; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016103 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 591; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016104 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 592; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016105 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 593; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016106 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 594; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016107 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 595; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016108 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 596; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016109 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 597; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016110 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 598; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016111 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 599; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016112 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 600; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016113 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 601; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016114 Genome-wide genotyping array 2022-08-18 35685441 Gyftopoulos A 2022-05-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/35685441 Identification of Novel Genetic Variants and Comorbidities Associated With ICD-10-Based Diagnosis of Hypertrophic Cardiomyopathy Using the UK Biobank Cohort. Hypertrophic cardiomyopathy (ICD-10 coded) 305 European ancestry cases, 11 African ancestry cases, 7 Caribbean ancestry cases, 40 cases, 7,260 European, African, Asian or unknown ancestry controls NA NR [12421579] (imputed) 2 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST90132261 Genome-wide genotyping array 2022-10-13 35842455 Tissink E 2022-07-16 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35842455 Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health. Total cerebellar volume 27,486 European ancestry individuals 3,906 European ancestry individuals Affymetrix [9380224] (imputed) 9 cerebellar volume measurement http://www.ebi.ac.uk/efo/EFO_0020864 GCST90105075 Genome-wide genotyping array 2022-10-13 35842455 Tissink E 2022-07-16 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35842455 Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health. Total cerebral volume 27,486 European ancestry individuals 3,906 European ancestry individuals Affymetrix [9380224] (imputed) 0 cerebral volume measurement http://www.ebi.ac.uk/efo/EFO_0021789 GCST90105076 Genome-wide genotyping array 2022-10-13 35842455 Tissink E 2022-07-16 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35842455 Genome-wide association study of cerebellar volume provides insights into heritable mechanisms underlying brain development and mental health. Total subcortical volume 27,486 European ancestry individuals 3,906 European ancestry individuals Affymetrix [9380224] (imputed) 0 subcortical volume measurement http://www.ebi.ac.uk/efo/EFO_0021790 GCST90105077 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 2; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015515 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 3; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015516 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 4; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015517 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 5; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015518 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 6; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015519 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 7; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015520 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 8; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015521 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 9; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015522 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 10; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015523 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 11; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015524 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 12; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015525 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 13; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015526 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 14; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015527 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 15; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015528 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 16; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015529 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 17; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015530 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 18; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015531 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 19; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015532 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 20; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015533 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 21; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015534 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 22; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015535 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 23; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015536 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 24; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015537 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 25; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015538 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 26; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015539 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 27; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015540 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 28; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015541 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 29; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015542 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 30; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015543 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 31; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015544 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 32; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015545 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 33; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015546 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 34; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015547 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 35; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015548 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 36; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015549 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 37; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015550 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 38; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015551 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 39; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015552 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 40; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015553 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 41; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015554 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 42; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015555 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 43; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015556 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 44; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015557 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 45; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015558 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 46; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015559 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 47; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015560 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 48; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015561 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 49; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015562 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 50; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015563 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 51; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015564 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 52; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015565 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 53; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015566 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 54; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015567 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 55; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015568 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 56; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015569 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 57; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015570 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 58; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015571 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 59; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015572 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 60; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015573 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 61; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015574 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 62; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015575 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 63; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015576 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 64; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015577 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 65; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015578 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 66; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015579 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 67; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015580 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 68; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015581 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 69; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015582 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 70; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015583 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 71; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015584 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 72; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015585 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 73; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015586 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 74; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015587 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 75; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015588 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 76; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015589 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 152; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015665 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 153; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015666 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 154; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015667 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 155; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015668 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 156; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015669 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 157; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015670 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 158; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015671 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 159; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015672 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 160; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015673 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 161; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015674 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 162; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015675 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 163; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015676 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 164; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015677 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 165; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015678 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 166; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015679 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 167; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015680 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 168; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015681 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 169; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015682 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 170; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015683 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 171; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015684 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 172; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015685 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 173; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015686 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 174; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015687 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 175; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015688 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 176; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015689 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 127; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015640 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 128; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015641 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 129; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015642 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 130; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015643 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 131; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015644 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 132; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015645 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 133; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015646 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 134; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015647 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 135; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015648 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 136; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015649 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 137; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015650 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 138; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015651 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 139; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015652 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 140; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015653 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 141; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015654 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 142; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015655 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 143; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015656 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 144; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015657 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 145; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015658 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 146; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015659 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 147; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015660 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 148; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015661 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 149; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015662 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 150; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015663 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 151; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015664 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 77; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015590 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 78; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015591 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 79; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015592 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 80; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015593 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 81; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015594 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 82; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015595 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 83; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015596 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 84; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015597 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 85; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015598 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 86; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015599 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 87; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015600 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 88; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015601 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 89; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015602 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 90; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015603 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 91; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015604 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 92; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015605 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 93; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015606 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 94; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015607 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 95; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015608 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 96; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015609 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 97; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015610 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 98; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015611 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 99; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015612 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 100; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015613 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 101; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015614 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 102; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015615 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 103; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015616 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 104; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015617 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 105; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015618 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 106; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015619 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 107; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015620 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 108; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015621 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 109; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015622 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 110; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015623 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 111; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015624 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 112; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015625 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 113; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015626 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 114; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015627 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 115; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015628 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 116; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015629 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 117; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015630 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 118; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015631 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 119; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015632 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 120; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015633 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 121; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015634 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 122; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015635 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 123; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015636 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 124; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015637 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 125; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015638 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 126; Facial segment 2; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90015639 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 188; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015701 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 189; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015702 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 190; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015703 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 191; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015704 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 192; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015705 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 193; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015706 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 232; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015745 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 233; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015746 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 234; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015747 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 235; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015748 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 236; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015749 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 237; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015750 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 238; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015751 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 239; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015752 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 177; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015690 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 178; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015691 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 179; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015692 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 180; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015693 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 181; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015694 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 182; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015695 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 183; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015696 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 184; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015697 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 185; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015698 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 186; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015699 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 187; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015700 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 277; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015790 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 278; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015791 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 279; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015792 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 280; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015793 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 281; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015794 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 282; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015795 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 240; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015753 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 241; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015754 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 242; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015755 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 243; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015756 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 244; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015757 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 245; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015758 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 246; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015759 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 247; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015760 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 248; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015761 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 249; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015762 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 250; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015763 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 251; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015764 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 252; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015765 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 253; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015766 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 254; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015767 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 255; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015768 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 256; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015769 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 257; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015770 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 258; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015771 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 194; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015707 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 195; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015708 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 196; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015709 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 197; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015710 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 198; Facial segment 3; 3D morphology of the upper and lower face, excluding the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015711 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 199; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015712 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 225; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015738 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 226; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015739 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 227; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015740 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 228; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015741 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 229; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015742 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 230; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015743 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 231; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015744 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 259; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015772 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 260; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015773 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 261; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015774 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 262; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015775 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 263; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015776 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 264; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015777 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 265; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015778 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 266; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015779 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 267; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015780 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 268; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015781 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 269; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015782 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 270; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015783 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 271; Facial segment 6; 3D morphology of the lower face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015784 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 272; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015785 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 273; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015786 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 274; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015787 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 275; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015788 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 276; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015789 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 200; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015713 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 201; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015714 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 202; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015715 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 203; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015716 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 204; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015717 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 205; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015718 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 206; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015719 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 207; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015720 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 208; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015721 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 209; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015722 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 210; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015723 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 211; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015724 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 212; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015725 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 213; Facial segment 4; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90015726 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 214; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015727 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 215; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015728 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 216; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015729 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 217; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015730 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 218; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015731 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 219; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015732 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 220; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015733 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 221; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015734 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 222; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015735 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 223; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015736 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 224; Facial segment 5; 3D morphology of the nose 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015737 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 283; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015796 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 284; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015797 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 285; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015798 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 286; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015799 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 287; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015800 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 288; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015801 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 289; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015802 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 290; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015803 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 291; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015804 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 292; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015805 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 293; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015806 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 294; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015807 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 295; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015808 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 296; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015809 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 297; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015810 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 298; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015811 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 299; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015812 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 300; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015813 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 301; Facial segment 7; 3D morphology of the upper face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90015814 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 702; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016215 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 703; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016216 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 704; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016217 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 705; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016218 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 706; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016219 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 707; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016220 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 708; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016221 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 709; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016222 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 710; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016223 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 711; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016224 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 712; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016225 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 713; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016226 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 714; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016227 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 715; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016228 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 716; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016229 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 717; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016230 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 718; Facial segment 31; 3D morphology of the cheekbones and temples 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016231 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 719; Facial segment 32; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016232 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 720; Facial segment 32; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016233 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 721; Facial segment 32; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016234 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 722; Facial segment 32; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016235 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 723; Facial segment 32; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016236 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 724; Facial segment 32; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016237 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 725; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016238 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 726; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016239 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 627; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016140 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 628; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016141 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 629; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016142 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 630; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016143 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 631; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016144 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 632; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016145 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 633; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016146 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 634; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016147 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 635; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016148 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 636; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016149 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 637; Facial segment 27; 3D morphology of the chin and inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016150 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 638; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016151 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 639; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016152 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 640; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016153 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 641; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016154 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 642; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016155 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 643; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016156 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 644; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016157 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 645; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016158 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 646; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016159 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 647; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016160 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 648; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016161 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 649; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016162 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 650; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016163 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 651; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016164 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 602; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016115 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 603; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016116 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 604; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016117 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 605; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016118 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 606; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016119 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 607; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016120 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 608; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016121 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 609; Facial segment 25; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016122 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 610; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016123 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 611; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016124 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 612; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016125 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 613; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016126 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 614; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016127 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 615; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016128 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 616; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016129 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 617; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016130 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 618; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016131 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 619; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016132 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 620; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016133 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 621; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016134 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 622; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016135 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 623; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016136 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 624; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016137 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 625; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016138 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 626; Facial segment 26; 3D morphology of the chin and outer jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016139 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 652; Facial segment 28; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016165 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 653; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016166 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 654; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016167 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 655; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016168 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 656; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016169 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 657; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016170 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 658; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016171 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 659; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016172 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 660; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016173 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 661; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016174 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 662; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016175 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 663; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016176 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 664; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016177 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 665; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016178 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 666; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016179 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 667; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016180 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 668; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016181 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 669; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016182 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 670; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016183 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 671; Facial segment 29; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016184 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 672; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016185 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 673; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016186 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 674; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016187 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 675; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016188 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 676; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016189 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 677; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016190 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 678; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016191 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 679; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016192 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 680; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016193 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 681; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016194 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 682; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016195 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 683; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016196 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 684; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016197 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 685; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016198 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 686; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016199 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 687; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016200 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 688; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016201 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 689; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016202 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 690; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016203 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 691; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016204 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 692; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016205 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 693; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016206 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 694; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016207 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 695; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016208 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 696; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016209 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 697; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016210 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 698; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016211 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 699; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016212 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 700; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016213 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 701; Facial segment 30; 3D morphology of the eyes 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016214 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 752; Facial segment 36; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016265 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 753; Facial segment 37; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016266 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 754; Facial segment 37; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016267 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 755; Facial segment 37; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016268 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 756; Facial segment 37; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016269 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 757; Facial segment 37; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016270 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 758; Facial segment 37; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016271 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 759; Facial segment 37; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016272 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 760; Facial segment 38; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016273 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 761; Facial segment 38; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016274 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 762; Facial segment 38; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016275 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 763; Facial segment 38; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016276 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 764; Facial segment 38; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016277 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 765; Facial segment 38; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016278 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 766; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016279 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 767; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016280 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 768; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016281 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 769; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016282 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 770; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016283 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 771; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016284 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 772; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016285 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 773; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016286 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 774; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016287 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 775; Facial segment 39; 3D morphology of the upper vermillion 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016288 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 776; Facial segment 40; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016289 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 827; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016340 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 828; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016341 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 829; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016342 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 830; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016343 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 831; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016344 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 832; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016345 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 833; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016346 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 834; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016347 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 835; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016348 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 836; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016349 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 837; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016350 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 838; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016351 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 839; Facial segment 45; 3D morphology of the nose alae 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016352 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 840; Facial segment 46; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016353 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 841; Facial segment 46; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016354 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 842; Facial segment 46; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016355 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 843; Facial segment 46; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016356 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 844; Facial segment 46; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016357 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 845; Facial segment 47; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016358 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 846; Facial segment 47; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016359 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 847; Facial segment 47; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016360 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 848; Facial segment 47; 3D morphology of the nose bridge 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016361 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 849; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016362 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 850; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016363 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 851; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016364 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 802; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016315 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 803; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016316 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 804; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016317 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 805; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016318 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 806; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016319 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 807; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016320 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 808; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016321 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 809; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016322 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 810; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016323 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 811; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016324 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 812; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016325 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 813; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016326 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 814; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016327 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 815; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016328 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 816; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016329 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 817; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016330 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 818; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016331 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 819; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016332 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 820; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016333 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 821; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016334 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 822; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 3 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016335 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 823; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016336 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 824; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016337 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 825; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016338 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 826; Facial segment 44; 3D morphology of the nose apex 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016339 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 727; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016240 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 728; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016241 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 729; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016242 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 730; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016243 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 731; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016244 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 732; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016245 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 733; Facial segment 33; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016246 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 734; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016247 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 735; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016248 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 736; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016249 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 737; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016250 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 738; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016251 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 739; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016252 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 740; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016253 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 741; Facial segment 34; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016254 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 742; Facial segment 35; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016255 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 743; Facial segment 35; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016256 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 744; Facial segment 35; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016257 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 745; Facial segment 35; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016258 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 746; Facial segment 35; 3D morphology of the upper lip 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016259 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 747; Facial segment 36; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016260 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 748; Facial segment 36; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016261 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 749; Facial segment 36; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016262 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 750; Facial segment 36; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016263 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 751; Facial segment 36; 3D morphology of the philtrium 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016264 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 852; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016365 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 853; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016366 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 854; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016367 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 855; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016368 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 856; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016369 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 857; Facial segment 48; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016370 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 858; Facial segment 49; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016371 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 859; Facial segment 49; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016372 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 860; Facial segment 49; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016373 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 861; Facial segment 49; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016374 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 862; Facial segment 49; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016375 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 863; Facial segment 49; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016376 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 864; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016377 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 865; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016378 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 866; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016379 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 867; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016380 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 868; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016381 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 869; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016382 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 870; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016383 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 871; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016384 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 872; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016385 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 873; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016386 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 874; Facial segment 50; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016387 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 875; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016388 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 876; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016389 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 777; Facial segment 40; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016290 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 778; Facial segment 40; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016291 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 779; Facial segment 40; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016292 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 780; Facial segment 40; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016293 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 781; Facial segment 40; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016294 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 782; Facial segment 40; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016295 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 783; Facial segment 41; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016296 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 784; Facial segment 41; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016297 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 785; Facial segment 41; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016298 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 786; Facial segment 41; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016299 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 787; Facial segment 41; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016300 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 788; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016301 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 789; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016302 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 790; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016303 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 791; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016304 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 792; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016305 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 793; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016306 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 794; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016307 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 795; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016308 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 796; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016309 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 797; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016310 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 798; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016311 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 799; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016312 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 800; Facial segment 42; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016313 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 801; Facial segment 43; 3D morphology of the nose sides 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 nose morphology measurement http://www.ebi.ac.uk/efo/EFO_0007843 GCST90016314 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 902; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016415 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 903; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016416 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 904; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016417 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 905; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016418 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 906; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016419 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 907; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016420 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 908; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016421 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 909; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016422 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 910; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016423 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 911; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016424 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 912; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016425 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 913; Facial segment 54; 3D morphology of the lower chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016426 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 914; Facial segment 55; 3D morphology of the inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016427 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 915; Facial segment 55; 3D morphology of the inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016428 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 916; Facial segment 55; 3D morphology of the inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016429 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 917; Facial segment 55; 3D morphology of the inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016430 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 918; Facial segment 55; 3D morphology of the inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016431 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 919; Facial segment 55; 3D morphology of the inner jaw 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 lower face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010948 GCST90016432 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 920; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016433 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 921; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016434 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 922; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016435 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 923; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016436 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 924; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016437 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 925; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016438 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 926; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016439 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 951; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016464 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 952; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016465 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 953; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016466 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 954; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016467 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 955; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016468 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 956; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016469 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 957; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016470 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 958; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016471 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 959; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016472 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 960; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016473 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 961; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016474 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 962; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016475 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 963; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016476 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 964; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016477 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 965; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016478 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 966; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016479 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 967; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016480 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 968; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016481 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 969; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016482 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 970; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016483 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 971; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016484 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 972; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016485 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 973; Facial segment 59; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016486 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 974; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016487 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 975; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016488 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 976; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016489 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 977; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016490 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 978; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016491 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 979; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016492 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 980; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016493 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 981; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016494 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 982; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016495 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 983; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016496 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 984; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016497 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 985; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016498 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 986; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016499 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 987; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016500 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 988; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016501 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 989; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016502 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 990; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016503 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 991; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016504 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 992; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016505 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 993; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016506 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 994; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016507 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 995; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016508 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 996; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016509 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 997; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016510 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 998; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016511 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 999; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016512 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1000; Facial segment 60; 3D morphology of the eye sockets 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016513 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 927; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016440 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 928; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016441 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 929; Facial segment 56; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016442 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 930; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016443 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 1; Facial segment 1; 3D morphology of the full face 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90015514 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 931; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016444 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 932; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016445 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 933; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016446 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 934; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016447 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 935; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016448 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 936; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016449 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 937; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016450 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 938; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016451 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 939; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016452 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 940; Facial segment 57; 3D morphology of the middle forehead 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016453 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 941; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016454 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 942; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016455 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 943; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016456 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 944; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016457 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 945; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016458 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 946; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016459 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 947; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016460 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 948; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016461 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 949; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016462 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 950; Facial segment 58; 3D morphology of the temple lines 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 upper face morphology measurement http://www.ebi.ac.uk/efo/EFO_0010949 GCST90016463 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 877; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016390 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 878; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016391 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 879; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016392 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 880; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016393 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 881; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016394 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 882; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016395 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 883; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016396 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 884; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016397 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 885; Facial segment 51; 3D morphology of the cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016398 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 886; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016399 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 887; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016400 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 888; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016401 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 889; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016402 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 890; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016403 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 891; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 2 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016404 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 892; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016405 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 893; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016406 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 894; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016407 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 895; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016408 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 896; Facial segment 52; 3D morphology of the outer cheeks 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016409 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 897; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016410 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 898; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016411 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 899; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016412 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 900; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016413 Genome-wide genotyping array 2022-07-18 33983923 Hoskens H 2021-05-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/33983923 3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies. Sib-shared facial trait 901; Facial segment 53; 3D morphology of the chin 8,246 European ancestry individuals NA Illumina [7417619] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90016414 Genome-wide genotyping array 2022-08-31 35959094 Dungan JR 2022-06-14 Am Heart J Plus www.ncbi.nlm.nih.gov/pubmed/35959094 Sex-dimorphic gene effects on survival outcomes in people with coronary artery disease. Survival in coronary artery disease 510 European ancestry males NA Illumina [785945] 8 survival time, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90133369 Genome-wide genotyping array 2022-08-31 35959094 Dungan JR 2022-06-14 Am Heart J Plus www.ncbi.nlm.nih.gov/pubmed/35959094 Sex-dimorphic gene effects on survival outcomes in people with coronary artery disease. Survival in coronary artery disease 174 European ancestry females NA Illumina [785945] 15 survival time, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90133370 Genome-wide genotyping array 2022-09-27 35942506 Jia P 2022-08-08 J Clin Hypertens (Greenwich) www.ncbi.nlm.nih.gov/pubmed/35942506 The genetic architecture of blood pressure variability: A genome-wide association study of 9370 participants from UK Biobank. Systolic blood pressure variability 9,370 European ancestry individuals NA Affymetrix [6884260] (imputed) 7 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90139385 Genome-wide genotyping array 2022-09-27 35942506 Jia P 2022-08-08 J Clin Hypertens (Greenwich) www.ncbi.nlm.nih.gov/pubmed/35942506 The genetic architecture of blood pressure variability: A genome-wide association study of 9370 participants from UK Biobank. Diastolic blood pressure variability 9,370 European ancestry individuals NA Affymetrix [6884260] (imputed) 8 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90139386 Genome-wide genotyping array 2022-09-30 36051697 Glessner JT 2022-08-16 Front Genet www.ncbi.nlm.nih.gov/pubmed/36051697 COVID-19 in pediatrics: Genetic susceptibility. COVID-19 498 African American cases, 1,533 African American controls NA Illumina [367556] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90128539 Genome-wide genotyping array 2022-09-30 36051697 Glessner JT 2022-08-16 Front Genet www.ncbi.nlm.nih.gov/pubmed/36051697 COVID-19 in pediatrics: Genetic susceptibility. COVID-19 271 European ancestry cases, 855 European ancestry controls NA Illumina [486109] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90128540 Genome-wide genotyping array 2022-09-30 36051697 Glessner JT 2022-08-16 Front Genet www.ncbi.nlm.nih.gov/pubmed/36051697 COVID-19 in pediatrics: Genetic susceptibility. COVID-19 498 African American cases, 1,533 African American controls, 271 European ancestry cases, 855 European ancestry controls NA Illumina [3854317] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90151687 Genome-wide genotyping array 2022-10-14 34562771 Lin JJ 2021-09-22 Biomed Pharmacother www.ncbi.nlm.nih.gov/pubmed/34562771 Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatment. Ribavirin-induced anemia in chronic hepatitis C 104 cases, 84 controls NA Illumina [291728] 8 anemia (phenotype), response to ribavirin http://www.ebi.ac.uk/efo/EFO_0004272, http://purl.obolibrary.org/obo/GO_1901559 GCST90053853 Genome-wide genotyping array 2022-08-24 35569502 Millischer V 2022-06-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/35569502 Improving lithium dose prediction using population pharmacokinetics and pharmacogenomics: a cohort genome-wide association study in Sweden. Lithium clearance 2,190 European or unknown individuals NA Affymetrix, Illumina [NR] (imputed) 8 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST90132628 Genome-wide genotyping array 2022-08-24 35569502 Millischer V 2022-06-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/35569502 Improving lithium dose prediction using population pharmacokinetics and pharmacogenomics: a cohort genome-wide association study in Sweden. Lithium clearance (adjusted for clinical predictors) 2,190 European or unknown individuals NA Affymetrix, Illumina [NR] (imputed) 11 response to lithium ion http://purl.obolibrary.org/obo/GO_0010226 GCST90132629 Genome-wide genotyping array 2022-08-26 35743677 Klumpers MJ 2022-05-28 J Pers Med www.ncbi.nlm.nih.gov/pubmed/35743677 Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury. eGFR decline after treatment with platinum based chemotherapy 195 European ancestry individuals NA Illumina [9799032] (imputed) 21 glomerular filtration rate, response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0004647 GCST90132622 Genome-wide genotyping array 2022-08-26 35743677 Klumpers MJ 2022-05-28 J Pers Med www.ncbi.nlm.nih.gov/pubmed/35743677 Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury. Acute kidney injury after treatment with platinum based chemotherapy 26 European ancestry cases, 169 European ancestry controls NA Illumina [9799032] (imputed) 3 response to platinum based chemotherapy, Acute kidney injury http://www.ebi.ac.uk/efo/EFO_0004647, http://purl.obolibrary.org/obo/HP_0001919 GCST90132623 Genome-wide genotyping array 2022-08-26 35743677 Klumpers MJ 2022-05-28 J Pers Med www.ncbi.nlm.nih.gov/pubmed/35743677 Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury. Lowest magnesium plasma levels after treatment with platinum based chemotherapy 163 European ancestry individuals NA Illumina [9799032] (imputed) 12 response to platinum based chemotherapy, magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004647, http://www.ebi.ac.uk/efo/EFO_0004845 GCST90132624 Genome-wide genotyping array 2022-08-26 35743677 Klumpers MJ 2022-05-28 J Pers Med www.ncbi.nlm.nih.gov/pubmed/35743677 Genome-Wide Analyses of Nephrotoxicity in Platinum-Treated Cancer Patients Identify Association with Genetic Variant in RBMS3 and Acute Kidney Injury. Hypomagnesemia after treatment with platinum based chemotherapy 38 European ancestry cases, 125 European ancestry controls NA Illumina [9799032] (imputed) 1 response to platinum based chemotherapy, Hypomagnesemia http://www.ebi.ac.uk/efo/EFO_0004647, http://purl.obolibrary.org/obo/HP_0002917 GCST90132626 Genome-wide genotyping array 2022-11-14 34985809 Kiewa J 2022-01-05 Depress Anxiety www.ncbi.nlm.nih.gov/pubmed/34985809 Perinatal depression is associated with a higher polygenic risk for major depressive disorder than non-perinatal depression. Perinatal depression 3,804 European ancestry cases, 6,134 European ancestry controls NA Illumina [7613370] (imputed) 23 asphyxia neonatorum http://www.ebi.ac.uk/efo/EFO_1000824 GCST90102433 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Mercuric chloride levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 mercuric chloride measurement http://www.ebi.ac.uk/efo/EFO_0022068 GCST90165243 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Mercuric chloride-2 levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 mercuric chloride measurement http://www.ebi.ac.uk/efo/EFO_0022068 GCST90165244 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Methoxychlor levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 methoxychlor measurement http://www.ebi.ac.uk/efo/EFO_0022069 GCST90165245 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Nickel levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 blood nickel measurement http://www.ebi.ac.uk/efo/EFO_0007583 GCST90165246 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Parathion levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 parathion measurement http://www.ebi.ac.uk/efo/EFO_0022070 GCST90165247 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Pentachlorophenol levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 pentachlorophenol measurement http://www.ebi.ac.uk/efo/EFO_0022071 GCST90165248 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (POD high) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165249 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (POD low) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165250 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Potassium chromate levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 potassium chromate measurement http://www.ebi.ac.uk/efo/EFO_0022072 GCST90165251 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (RfD high) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165252 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (RfD low) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165253 Genome-wide genotyping array 2022-08-26 35970579 Grover S 2022-05-26 Neurology www.ncbi.nlm.nih.gov/pubmed/35970579 Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium. Age of onset of parkinson disease 7,847 European ancestry individuals, 688 East Asian ancestry individuals NA Illumina [NR] (imputed) 2 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST90133315 Genome-wide genotyping array 2022-08-26 35970579 Grover S 2022-05-26 Neurology www.ncbi.nlm.nih.gov/pubmed/35970579 Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium. Age of onset of parkinson disease 7,847 European ancestry individuals, 688 East Asian ancestry individuals, 17,415 individuals NA Illumina [NR] (imputed) 5 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST90133316 Genome-wide genotyping array 2019-01-31 27476799 Nielson CM 2016-09-06 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/27476799 Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2. Lumbar spine bone mineral density (trabecular) 12,287 European ancestry individuals 2,987 individuals Affymetrix, Illumina [up to 37790451] (imputed) 12 volumetric bone mineral density http://www.ebi.ac.uk/efo/EFO_0007620 GCST007014 Genome-wide genotyping array 2019-01-31 27476799 Nielson CM 2016-09-06 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/27476799 Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2. Lumbar spine bone mineral density (integral) 11,080 European ancestry individuals NA Affymetrix, Illumina [up to 2659730] (imputed) 20 volumetric bone mineral density http://www.ebi.ac.uk/efo/EFO_0007620 GCST007015 Genome-wide genotyping array 2019-02-19 30363675 Cha EDK 2018-09-27 J Obes www.ncbi.nlm.nih.gov/pubmed/30363675 Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery. Subcutaneous adipose tissue 2,545 European ancestry individuals NA Illumina [629675] 1 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST007190 Genome-wide genotyping array 2019-02-19 30363675 Cha EDK 2018-09-27 J Obes www.ncbi.nlm.nih.gov/pubmed/30363675 Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery. Visceral adipose tissue 2,545 European ancestry individuals NA Illumina [629675] 1 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST007187 Genome-wide genotyping array 2019-02-19 30363675 Cha EDK 2018-09-27 J Obes www.ncbi.nlm.nih.gov/pubmed/30363675 Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery. Visceral adipose tissue/subcutaneous adipose tissue ratio 2,545 European ancestry individuals NA Illumina [629675] 1 visceral:subcutaneous adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0004767 GCST007188 Genome-wide genotyping array 2019-02-19 30363675 Cha EDK 2018-09-27 J Obes www.ncbi.nlm.nih.gov/pubmed/30363675 Using Adipose Measures from Health Care Provider-Based Imaging Data for Discovery. visceral adipose tissue/total adipose tissue ratio 2,545 European ancestry individuals NA Illumina [629675] 1 visceral:total adipose tissue ratio http://www.ebi.ac.uk/efo/EFO_0009701 GCST007189 Genome-wide genotyping array 2019-07-12 29273807 Turcot V 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273807 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Body mass index up to 449,889 European ancestry individuals, up to 29,398 South Asian ancestry individuals, up to 27,610 African American individuals, up to 8,839 East Asian individuals, up to 10,772 Hispanic ancestry individuals up to 196,766 European ancestry individuals Illumina [246328] 92 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008129 Genome-wide genotyping array, Targeted genotyping array [Exome array] 2019-07-12 29273807 Turcot V 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273807 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Body mass index up to 449,889 European ancestry individuals up to 192,226 European ancestry individuals Illumina [246328] 5 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008128 Genome-wide genotyping array, Targeted genotyping array [Exome array] 2019-07-12 29273807 Turcot V 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273807 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Body mass index up to 27,610 African American individuals up to 192,226 European ancestry individuals Illumina [246328] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008124 Genome-wide genotyping array, Targeted genotyping array [Exome array] 2019-07-12 29273807 Turcot V 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273807 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Body mass index up to 8,839 East Asian ancestry individuals NA Illumina [246328] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008126 Genome-wide genotyping array, Targeted genotyping array [Exome array] 2019-07-12 29273807 Turcot V 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273807 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Body mass index up to 29,398 South Asian ancestry individuals NA Illumina [246328] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008127 Genome-wide genotyping array, Targeted genotyping array [Exome array] 2019-07-12 29273807 Turcot V 2017-12-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29273807 Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity. Body mass index up to 10,772 Hispanic individuals NA Illumina [246328] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST008125 Genome-wide genotyping array, Targeted genotyping array [Exome array] 2018-10-17 30070759 Olsson M 2018-08-02 J Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/30070759 Genome-wide analysis of genetic determinants of circulating factor VII activating protease (FSAP) activity. Plasma factor VII activating protease levels 3,126 Swedish ancestry individuals NA Illumina [~ 10000000] (imputed) 43 factor VII activating protease measurement http://www.ebi.ac.uk/efo/EFO_0009368 GCST006417 Genome-wide genotyping array 2019-04-25 30920136 Stapleton CP 2019-02-27 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/30920136 The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population. Estimated glomerular filtration rate after 1 year in renal transplantation (donor effect) Up to 4,475 European ancestry individuals NA Illumina [up to 3791089] (imputed) 6 glomerular filtration rate, renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST007644 Genome-wide genotyping array 2019-04-25 30920136 Stapleton CP 2019-02-27 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/30920136 The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population. Estimated glomerular filtration rate after 5 years in renal transplantation (recipient effect) Up to 2,921 European ancestry individuals NA Illumina [up to 3935887] (imputed) 10 glomerular filtration rate, renal transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0005199 GCST007649 Genome-wide genotyping array 2019-04-25 30920136 Stapleton CP 2019-02-27 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/30920136 The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population. Estimated glomerular filtration rate after 5 years in renal transplantation (donor effect) Up to 2,921 European ancestry individuals NA Illumina [up to 3951530] (imputed) 7 glomerular filtration rate, renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST007648 Genome-wide genotyping array 2019-04-25 30920136 Stapleton CP 2019-02-27 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/30920136 The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population. Estimated glomerular filtration rate change in renal transplantation (recipient effect) Up to 2,298 European ancestry individuals NA Illumina [up to 3923932] (imputed) 6 glomerular filtration rate, renal transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0005199 GCST007647 Genome-wide genotyping array 2019-04-25 30920136 Stapleton CP 2019-02-27 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/30920136 The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population. Estimated glomerular filtration rate change in renal transplantation (donor effect) Up to 2,298 European ancestry individuals NA Illumina [up to 3936786] (imputed) 2 glomerular filtration rate, renal transplant outcome measurement, donor genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0005199, http://www.ebi.ac.uk/efo/EFO_0007892 GCST007646 Genome-wide genotyping array 2019-04-25 30920136 Stapleton CP 2019-02-27 Am J Transplant www.ncbi.nlm.nih.gov/pubmed/30920136 The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population. Estimated glomerular filtration rate after 1 year in renal transplantation (recipient effect) Up to 5,935 European ancestry individuals NA Illumina [up to 3803121] (imputed) 7 glomerular filtration rate, renal transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0005199 GCST007645 Genome-wide genotyping array 2019-02-11 30242241 Hachiya T 2018-09-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30242241 Genome-wide analysis of polymorphism × sodium interaction effect on blood pressure identifies a novel 3'-BCL11B gene desert locus. Systolic blood pressure x sodium interaction (1df test) 4,527 Japanese ancestry individuals 4,241 Japanese ancestry individuals Illumina [7135436] (imputed) 1 sodium measurement, systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006335 GCST007108 Genome-wide genotyping array 2019-02-11 30242241 Hachiya T 2018-09-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30242241 Genome-wide analysis of polymorphism × sodium interaction effect on blood pressure identifies a novel 3'-BCL11B gene desert locus. Diastolic blood pressure x sodium interaction (1df test) 4,527 Japanese ancestry individuals 4,241 Japanese ancestry individuals Illumina [7135436] (imputed) 3 sodium measurement, diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0009282, http://www.ebi.ac.uk/efo/EFO_0006336 GCST007107 Genome-wide genotyping array 2020-11-24 30938820 Qian M 2019-04-02 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/30938820 Genome-wide association study of susceptibility loci for T-cell acute lymphoblastic leukemia in children. T-cell acute lymphoblastic leukaemia 157 African American child cases, 699 European ancestry child cases, 126 Hispanic child cases, 209 child cases, 12,178 European, African American and unknown ancestry controls 26 African American child cases, 75 European ancestry child cases, 9 Hispanic child cases, 7 child cases, 5,518 European, African American and unknown ancestry controls Affymetrix, Illumina [7967910] (imputed) 0 childhood T acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_1001947 GCST010756 Genome-wide genotyping array 2018-10-18 30134803 Matana A 2018-04-11 Mol Med www.ncbi.nlm.nih.gov/pubmed/30134803 Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level. Plasma parathyroid hormone levels 806 Korculan (founder/genetic isolate) individuals, 831 Vis (founder/genetic isolate) individuals, 959 Croatian ancestry individuals NA Illumina [7411206] (imputed) 30 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST006431 Genome-wide genotyping array 2019-04-30 30899065 Wang M 2019-03-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30899065 A genome-wide association study on photic sneeze reflex in the Chinese population. Photic sneeze reflex 874 Chinese ancestry cases, 2,543 Chinese ancestry controls NA Affymetrix [419093] 3 autosomal dominant compelling helio-ophthalmic outburst syndrome http://www.ebi.ac.uk/efo/EFO_0007887 GCST007687 Genome-wide genotyping array 2019-07-16 30899057 Lee MG 2019-03-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30899057 Integrative Genome-Wide Association Studies of eQTL and GWAS Data for Gout Disease Susceptibility. Gout 373 Han Chinese ancestry cases, 6,721 Han Chinese ancestry controls 385 Han Chinese ancestry cases, 7,445 Han Chinese ancestry controls Affymetrix [607675] 3 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST008139 Genome-wide genotyping array 2019-01-08 30132804 Kim M 2018-08-22 Clin Genet www.ncbi.nlm.nih.gov/pubmed/30132804 APOA5 Variants are Associated with Decreased Adiponectin Levels and Increased Arterial Stiffness in Subjects with Low HDL-cholesterol Levels. Low HDL-cholesterol levels 612 Korean ancestry cases, 1,536 Korean ancestry controls NA Affymetrix [394411] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST006860 Genome-wide genotyping array 2021-06-08 33213513 Ibanez L 2020-11-19 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/33213513 Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease. Cerebrospinal fluid t-tau levels 1,338 European ancestry individuals NA Illumina [NR] (imputed) 15 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST011821 Genome-wide genotyping array, Genome-wide sequencing 2021-06-08 33213513 Ibanez L 2020-11-19 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/33213513 Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease. Cerebrospinal P-tau181p levels 1,338 European ancestry individuals NA Illumina [NR] (imputed) 10 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST011820 Genome-wide genotyping array, Genome-wide sequencing 2021-06-08 33213513 Ibanez L 2020-11-19 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/33213513 Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease. Cerebrospinal fluid AB1-42 levels 1,338 European ancestry individuals NA Illumina [NR] (imputed) 23 beta-amyloid 1-42 measurement http://www.ebi.ac.uk/efo/EFO_0004670 GCST011819 Genome-wide genotyping array, Genome-wide sequencing 2021-06-08 33213513 Ibanez L 2020-11-19 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/33213513 Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease. Alpha synuclein levels (MTAG) 1744 European ancestry individuals NA Illumina [NR] (imputed) 11 alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0009323 GCST011818 Genome-wide genotyping array 2021-06-08 33213513 Ibanez L 2020-11-19 Acta Neuropathol Commun www.ncbi.nlm.nih.gov/pubmed/33213513 Functional genomic analyses uncover APOE-mediated regulation of brain and cerebrospinal fluid beta-amyloid levels in Parkinson disease. Cerebrospinal fluid α-synuclein levels 1,960 European ancestry individuals NA Illumina [NR] (imputed) 4 alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0009323 GCST011822 Genome-wide genotyping array, Genome-wide sequencing 2018-09-28 30045251 Lee MR 2018-07-01 Medicine (Baltimore) www.ncbi.nlm.nih.gov/pubmed/30045251 Causal association of body mass index with hypertension using a Mendelian randomization design. Body mass index 8,832 Korean ancestry individuals NA Affymetrix [1590162] (imputed) 10 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST006369 Genome-wide genotyping array 2021-04-21 33589590 Marshe VS 2021-02-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33589590 Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response. Remission after antidepressant treatment in major depression 161 European ancestry remitters, 11 African ancestry remitters, 2 other or admixed ancestry remitters, 146 European ancestry non-remitters, 11 African ancestry non-remitters, 4 other or admixed ancestry non-remitters 443 European ancestry remitters, 34 remitters, 492 European ancestry non-remitters, 77 non-remitters Illumina [4471676] (imputed) 0 remission, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0009785, http://purl.obolibrary.org/obo/GO_0036276 GCST011533 Genome-wide genotyping array 2021-04-21 33589590 Marshe VS 2021-02-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33589590 Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response. Response to antidepressants (symptom improvement) 307 European ancestry individuals NA Illumina [4471676] (imputed) 7 depressive symptom measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007006, http://purl.obolibrary.org/obo/GO_0036276 GCST011528 Genome-wide genotyping array 2021-04-21 33589590 Marshe VS 2021-02-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33589590 Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response. Response to antidepressants (symptom improvement) 22 African ancestry individuals NA Illumina [4471676] (imputed) 0 depressive symptom measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007006, http://purl.obolibrary.org/obo/GO_0036276 GCST011529 Genome-wide genotyping array 2021-04-21 33589590 Marshe VS 2021-02-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33589590 Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response. Response to antidepressants (symptom improvement) 307 European ancestry individuals, 22 African ancestry individuals, 6 other or admixed ancestry individuals 935 European ancestry individuals, 111 individuals Illumina [4471676] (imputed) 0 depressive symptom measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007006, http://purl.obolibrary.org/obo/GO_0036276 GCST011530 Genome-wide genotyping array 2021-04-21 33589590 Marshe VS 2021-02-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33589590 Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response. Remission after antidepressant treatment in major depression 161 European ancestry remitters, 146 European ancestry non-remitters NA Illumina [4471676] (imputed) 3 remission, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0009785, http://purl.obolibrary.org/obo/GO_0036276 GCST011531 Genome-wide genotyping array 2021-04-21 33589590 Marshe VS 2021-02-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33589590 Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response. Remission after antidepressant treatment in major depression 11 African ancestry remitters, 11 African ancestry non-remitters NA Illumina [4471676] (imputed) 0 remission, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0009785, http://purl.obolibrary.org/obo/GO_0036276 GCST011532 Genome-wide genotyping array 2018-09-19 30066433 Jabbari E 2018-07-31 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/30066433 Variation at the TRIM11 locus modifies Progressive Supranuclear Palsy phenotype. Non-Richardson's syndrome vs Richardson's syndrome in progressive supranuclear palsy 130 European ancestry non-Richardson's syndrome cases, 367 European ancestry Richardson's syndrome controls NA Illumina [6215948] (imputed) 2 progressive supranuclear palsy http://purl.obolibrary.org/obo/MONDO_0019037 GCST006276 Genome-wide genotyping array 2019-03-11 30659475 Arias-Vasquez A 2019-01-18 Behav Genet www.ncbi.nlm.nih.gov/pubmed/30659475 A Potential Role for the STXBP5-AS1 Gene in Adult ADHD Symptoms. Attention deficit hyperactivity disorder symptom score 14,689 European ancestry adults, 14,776 children NA Affymetrix, Illumina, Perlegen [2804754] (imputed) 1 ADHD symptom measurement http://www.ebi.ac.uk/efo/EFO_0007860 GCST007279 Genome-wide genotyping array 2018-10-17 30061737 Nielsen JB 2018-07-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30061737 Biobank-driven genomic discovery yields new insight into atrial fibrillation biology. Atrial fibrillation 60,620 European ancestry cases, 970,216 European ancestry controls NA Illumina [34740186] (imputed) 142 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST006414 Genome-wide genotyping array 2019-01-29 30642363 Hoffman J 2019-01-14 Breast Cancer Res www.ncbi.nlm.nih.gov/pubmed/30642363 Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas. Breast cancer 2,385 Latina cases, 6,416 Latina controls 2,412 Latina cases, 1,580 Latina controls, 3,153 African American cases, 2,831 African American controls, 1,657 African, African American and West Indian cases, 2,029 African, African American and West Indian controls, 4,525 East Asian ancestry cases, 4,194 East Asian ancestry controls, European ancestry cases, European ancestry controls Affymetrix, Illumina [at least 192795] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST006985 Genome-wide genotyping array 2019-05-08 30895295 Jonnalagadda M 2019-03-21 Genome Biol Evol www.ncbi.nlm.nih.gov/pubmed/30895295 A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry. Skin reflectance (Melanin index) 720 South Asian ancestry individuals Affymetrix, Illumina [at least 398118] (imputed) 63 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST007739 Genome-wide genotyping array 2019-05-08 30895295 Jonnalagadda M 2019-03-21 Genome Biol Evol www.ncbi.nlm.nih.gov/pubmed/30895295 A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry. Iris color (a* coordinate) 329 South Asian ancestry individuals Illumina [640625] (imputed) 34 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007740 Genome-wide genotyping array 2019-05-08 30895295 Jonnalagadda M 2019-03-21 Genome Biol Evol www.ncbi.nlm.nih.gov/pubmed/30895295 A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry. Iris color (b* coordinate) 329 South Asian ancestry individuals Illumina [640625] (imputed) 45 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007741 Genome-wide genotyping array 2019-05-08 30895295 Jonnalagadda M 2019-03-21 Genome Biol Evol www.ncbi.nlm.nih.gov/pubmed/30895295 A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry. Iris color (L* coordinate) 329 South Asian ancestry individuals Illumina [640625] (imputed) 42 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007743 Genome-wide genotyping array 2019-05-08 30895295 Jonnalagadda M 2019-03-21 Genome Biol Evol www.ncbi.nlm.nih.gov/pubmed/30895295 A genome-wide association study of skin and iris pigmentation among individuals of South Asian ancestry. Iris heterochromicity 329 South Asian ancestry individuals Illumina [640625] (imputed) 37 eye colour measurement http://www.ebi.ac.uk/efo/EFO_0009764 GCST007742 Genome-wide genotyping array 2019-05-14 30929738 Ferreira MAR 2019-03-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30929738 Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. Asthma (childhood onset) 13,962 European ancestry cases, 300,671 European ancestry controls 31,759 European ancestry cases, 214,890 European ancestry controls Affymetrix [9000000] (imputed) 105 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST007800 Genome-wide genotyping array 2019-05-14 30929738 Ferreira MAR 2019-03-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30929738 Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. Asthma (adult onset) 26,582 European ancestry cases, 300,671 European ancestry controls 16,297 European ancestry cases, 217,711 European ancestry controls Affymetrix [9000000] (imputed) 46 adult onset asthma http://www.ebi.ac.uk/efo/EFO_1002011 GCST007799 Genome-wide genotyping array 2019-05-14 30929738 Ferreira MAR 2019-03-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30929738 Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. Asthma 40,544 European ancestry cases, 300,671 European ancestry controls NA Affymetrix [9000000] (imputed) 160 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007798 Genome-wide genotyping array 2019-05-14 30929738 Ferreira MAR 2019-03-28 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30929738 Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. Asthma onset (childhood vs adult) 13,962 European ancestry childhood onset cases, 14,873 European ancestry adult onset cases 31,002 European ancestry childhood onset cases, 16,297 European ancestry adult onset cases Affymetrix [9000000] (imputed) 55 age of onset of asthma http://purl.obolibrary.org/obo/OBA_2001001 GCST007797 Genome-wide genotyping array 2019-03-06 30787307 Daya M 2019-02-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30787307 Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations. Adult asthma 4,235 African American Afro-Caribbean cases, 5,283 African American Afro-Caribbean controls, 2774 Hispanic cases, 2,362 Hispanic controls NA Affymetrix, Illumina [23328733] (imputed) 11 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST007266 Genome-wide genotyping array 2018-07-19 29608257 Painter JN 2018-04-02 Cancer Med www.ncbi.nlm.nih.gov/pubmed/29608257 Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses. Endometriosis or endometrial cancer (pleiotropy) 3,194 endometriosis cases, 5,330 non-endometriosis controls, 2,057 endometrial cancer cases, 3,866 non-endometrial cancer controls NA Illumina [462430] 8 endometrial carcinoma, endometriosis http://www.ebi.ac.uk/efo/EFO_1001512, http://www.ebi.ac.uk/efo/EFO_0001065 GCST005906 Genome-wide genotyping array 2019-05-01 24629169 Ising M 2014-04-08 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24629169 Genetic effects on information processing speed are moderated by age--converging results from three samples. Executive function (trail making test B) 890 European ancestry individuals NA Illumina [~ 290000] 1 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST007694 Genome-wide genotyping array 2019-05-01 24629169 Ising M 2014-04-08 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24629169 Genetic effects on information processing speed are moderated by age--converging results from three samples. Perceptual and visual search speed and executive function (trail making test BA) 890 European ancestry individuals NA Illumina [~ 290000] 0 executive function measurement, information processing speed http://www.ebi.ac.uk/efo/EFO_0009332, http://www.ebi.ac.uk/efo/EFO_0004363 GCST007695 Genome-wide genotyping array 2019-05-01 24629169 Ising M 2014-04-08 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24629169 Genetic effects on information processing speed are moderated by age--converging results from three samples. perceptual and visual search speed (trail making test A) (age interaction) 890 European ancestry individuals NA Illumina [~ 290000] 1 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST007696 Genome-wide genotyping array 2019-05-01 24629169 Ising M 2014-04-08 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24629169 Genetic effects on information processing speed are moderated by age--converging results from three samples. Executive function (trail making test B) (age interaction) 890 European ancestry individuals NA Illumina [~ 290000] 0 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST007697 Genome-wide genotyping array 2019-05-01 24629169 Ising M 2014-04-08 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24629169 Genetic effects on information processing speed are moderated by age--converging results from three samples. Perceptual and visual search speed and executive function (trail making test BA) (age interaction) 890 European ancestry individuals NA Illumina [~ 290000] 0 executive function measurement, information processing speed http://www.ebi.ac.uk/efo/EFO_0009332, http://www.ebi.ac.uk/efo/EFO_0004363 GCST007698 Genome-wide genotyping array 2019-05-01 24629169 Ising M 2014-04-08 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/24629169 Genetic effects on information processing speed are moderated by age--converging results from three samples. Perceptual and visual search speed (trail making test A) 890 European ancestry individuals NA Illumina [~ 290000] 2 information processing speed http://www.ebi.ac.uk/efo/EFO_0004363 GCST007693 Genome-wide genotyping array 2019-04-25 30945673 Prasad G 2019-03-01 J Genet www.ncbi.nlm.nih.gov/pubmed/30945673 Genomewide association study for C-reactive protein in Indians replicates known associations of common variants. Postoperative survival time in hepatocellular carcinoma 367 East Asian ancestry individuals 758 East Asian ancestry individuals Affymetrix [630573] 5 overall survival http://www.ebi.ac.uk/efo/EFO_0000638 GCST007650 Genome-wide genotyping array 2019-08-28 30972912 Wei L 2019-04-10 J Viral Hepat www.ncbi.nlm.nih.gov/pubmed/30972912 Genetic variation in FCER1A predicts peginterferon alfa-2a-induced hepatitis B surface antigen clearance in East Asian patients with chronic hepatitis B. Peginterferon alfa-2a treatment response in chronic hepatitis B infection up to 1,108 East Asian cases, up to 465 European ancestry cases, up to 63 cases NA Illumina [> 750000] 27 response to peginterferon alfa-2a http://www.ebi.ac.uk/efo/EFO_0010103 GCST008514 Genome-wide genotyping array 2019-05-17 30975718 Tanikawa C 2019-04-11 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/30975718 Novel Risk Loci Identified in a Genome-Wide Association Study of Urolithiasis in a Japanese Population. Urolithiasis 11,130 Japanese ancestry cases, 187,639 Japanese ancestry controls 2,289 Japanese ancestry cases, 3,817 Japanese ancestry controls Illumina [6603247] (imputed) 17 urolithiasis http://purl.obolibrary.org/obo/MONDO_0024647 GCST007833 Genome-wide genotyping array 2019-08-01 30971808 Kim JJ 2019-04-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30971808 Identification of SAMD9L as a susceptibility locus for intravenous immunoglobulin resistance in Kawasaki disease by genome-wide association analysis. Response to intravenous immunoglobulin treatment in Kawasaki disease 101 Korean ancestry non-responder cases, 195 Korean ancestry responder cases 216 East Asian ancestry non-responder cases, 1,026 East Asian responder cases Illumina [721341] 1 response to intravenous immunoglobulin therapy http://www.ebi.ac.uk/efo/EFO_0010065 GCST008314 Genome-wide genotyping array 2019-04-30 30911093 Bandesh K 2019-03-25 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30911093 Genome-wide association study of blood lipids in Indians confirms universality of established variants. Low density lipoprotein cholesterol levels 1,036 Indian ancestry individuals 4,235 Indian ancestry individuals, 188,577 European ancestry individuals, 7,898 East Asian, South Asian and African ancestry individuals Illumina [551825] 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST007689 Genome-wide genotyping array 2019-05-02 30911093 Bandesh K 2019-03-25 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30911093 Genome-wide association study of blood lipids in Indians confirms universality of established variants. High density lipoprotein cholesterol levels 1,036 Indian ancestry individuals 4,235 Indian ancestry individuals, 188,577 European ancestry individuals, 7,898 East Asian, South Asian and African ancestry individuals Illumina [551825] 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007701 Genome-wide genotyping array 2019-05-02 30911093 Bandesh K 2019-03-25 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30911093 Genome-wide association study of blood lipids in Indians confirms universality of established variants. Triglyceride levels 1,036 Indian ancestry individuals 4,235 Indian ancestry individuals, 188,577 European ancestry individuals, 7,898 East Asian, South Asian and African ancestry individuals Illumina [551825] 10 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST007702 Genome-wide genotyping array 2019-04-30 30911093 Bandesh K 2019-03-25 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30911093 Genome-wide association study of blood lipids in Indians confirms universality of established variants. Total cholesterol levels 1,036 Indian ancestry individuals 4,235 Indian ancestry individuals, 188,577 European ancestry individuals, 7,898 East Asian, South Asian and African ancestry individuals Illumina [551825] 2 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST007688 Genome-wide genotyping array 2019-05-16 28234671 Nandakumar P 2017-07-01 J Hypertens www.ncbi.nlm.nih.gov/pubmed/28234671 Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry. Systolic blood pressure 11,156 African American individuals, 4,758 African ancestry individuals NA Illumina [105487] 7 systolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006944 GCST007829 Targeted genotyping array [Exome array] 2019-05-16 28234671 Nandakumar P 2017-07-01 J Hypertens www.ncbi.nlm.nih.gov/pubmed/28234671 Rare coding variants associated with blood pressure variation in 15 914 individuals of African ancestry. Diastolic blood pressure 11,156 African American individuals, 4,758 African ancestry individuals NA Illumina [105487] 2 diastolic blood pressure change measurement http://www.ebi.ac.uk/efo/EFO_0006945 GCST007828 Targeted genotyping array [Exome array] 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Serum alkaline phosphatase levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 55 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST011353 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Total cholesterol levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 69 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST011346 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Alanine aminotransferase levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 40 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST011352 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Aspartate aminotransferase levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 25 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST011351 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. C-reactive protein levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 18 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST011350 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Gamma glutamyl transferase levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 50 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST011349 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. High density lipoprotein cholesterol levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 72 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST011348 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Low density lipoprotein cholesterol levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 63 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST011347 Genome-wide genotyping array 2021-03-22 33339817 Nielsen JB 2020-12-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33339817 Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease. Triglyceride levels 76,081 European ancestry individuals, 127,395 Japanese ancestry individuals NA Illumina [31500000] (imputed) 37 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011345 Genome-wide genotyping array 2021-07-27 33455090 Bing N 2021-01-17 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/33455090 Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses. Response to tofacitinib treatment in rheumatoid arthritis (herpes zoster)(time to event) 165 European ancestry cases, 2,023 European ancestry controls, 56 East Asian ancestry cases, 237 East Asian ancestry controls, 23 Hispanic cases, 399 Hispanic controls NA Illumina [up to 8000000] (imputed) 4 Herpes Zoster, response to tofacitinib http://www.ebi.ac.uk/efo/EFO_0006510, http://www.ebi.ac.uk/efo/EFO_0600024 GCST012086 Genome-wide genotyping array 2021-07-27 33455090 Bing N 2021-01-17 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/33455090 Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses. Response to tofacitinib treatment in psoriasis (herpes zoster)(time to event) 56 European ancestry cases, 1,543 European ancestry controls, 10 East Asian ancestry cases, 80 East Asian ancestry controls, 4 Hispanic cases, 245 Hispanic controls NA Illumina [up to 8000000] (imputed) 4 Herpes Zoster, response to tofacitinib http://www.ebi.ac.uk/efo/EFO_0006510, http://www.ebi.ac.uk/efo/EFO_0600024 GCST012085 Genome-wide genotyping array 2021-07-27 33455090 Bing N 2021-01-17 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/33455090 Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses. Response to tofacitinib treatment in rheumatoid arthritis (herpes zoster) 165 European ancestry cases, 2,023 European ancestry controls, 56 East Asian ancestry cases, 237 East Asian ancestry controls, 23 Hispanic cases, 399 Hispanic controls NA Illumina [up to 8000000] (imputed) 4 Herpes Zoster, response to tofacitinib http://www.ebi.ac.uk/efo/EFO_0006510, http://www.ebi.ac.uk/efo/EFO_0600024 GCST012084 Genome-wide genotyping array 2021-07-27 33455090 Bing N 2021-01-17 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/33455090 Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses. Response to tofacitinib treatment in psoriasis (herpes zoster) 56 European ancestry cases, 1,543 European ancestry controls, 10 East Asian ancestry cases, 80 East Asian ancestry controls, 4 Hispanic cases, 245 Hispanic controls NA Illumina [up to 8000000] (imputed) 3 Herpes Zoster, response to tofacitinib http://www.ebi.ac.uk/efo/EFO_0006510, http://www.ebi.ac.uk/efo/EFO_0600024 GCST012083 Genome-wide genotyping array 2021-07-27 33455090 Bing N 2021-01-17 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/33455090 Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses. Response to tofacitinib treatment (herpes zoster)(time to event) 165 European ancestry rheumatoid arthritis cases, 56 East Asian ancestry rheumatoid arthritis cases, 23 Hispanic rheumatoid arthritis cases, 56 European ancestry psoriasis cases, 10 East Asian ancestry psoriasis cases, 4 Hispanic psoriasis cases, 3,566 European ancestry controls, 317 East Asian ancestry controls, 644 Hispanic controls NA Illumina [up to 8000000] (imputed) 5 Herpes Zoster, response to tofacitinib http://www.ebi.ac.uk/efo/EFO_0006510, http://www.ebi.ac.uk/efo/EFO_0600024 GCST012082 Genome-wide genotyping array 2021-07-27 33455090 Bing N 2021-01-17 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/33455090 Contribution of a European-Prevalent Variant near CD83 and an East Asian-Prevalent Variant near IL17RB to Herpes Zoster Risk in Tofacitinib Treatment: Results of Genome-Wide Association Study Meta-Analyses. Response to tofacitinib treatment (herpes zoster) 165 European ancestry rheumatoid arthritis cases, 56 East Asian ancestry rheumatoid arthritis cases, 23 Hispanic rheumatoid arthritis cases, 56 European ancestry psoriasis cases, 10 East Asian ancestry psoriasis cases, 4 Hispanic psoriasis cases, 3,566 European ancestry controls, 317 East Asian ancestry controls, 644 Hispanic controls NA Illumina [up to 8000000] (imputed) 5 Herpes Zoster, response to tofacitinib http://www.ebi.ac.uk/efo/EFO_0006510, http://www.ebi.ac.uk/efo/EFO_0600024 GCST012081 Genome-wide genotyping array 2019-02-20 30317457 Bonnemaijer PWM 2018-10-13 Hum Genet www.ncbi.nlm.nih.gov/pubmed/30317457 Genome-wide association study of primary open-angle glaucoma in continental and admixed African populations. Glaucoma (primary open-angle) 484 Sub-Saharan African ancestry cases, 179 South African Coloured ancestry cases, 450 African American cases, 380 Sub-Saharan African ancestry controls, 96 South African Coloured ancestry controls, 1350 African American controls 1,993 Sub-Saharan African ancestry cases, 2,595 African American cases, 1,730 Sub-Saharan African ancestry controls, 2,813 African American controls Illumina [~ 13800000] (imputed) 1 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST007199 Genome-wide genotyping array 2022-07-07 35368043 Chang D 2022-04-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35368043 A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk. Asthma (moderate or severe) 3,181 European ancestry cases, 3,590 European ancestry controls NA Illumina [10766565] 10 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90105078 Genome-wide sequencing 2021-07-27 33479212 Yao X 2021-01-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33479212 Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Attention deficit hyperactivity disorder (MTAG) at least 19,099 European ancestry cases, at least 34,194 European ancestry controls 2,726 European ancestry cases, 16,299 European ancestry controls NR [NR] 9 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST012093 Genome-wide genotyping array 2021-07-27 33479212 Yao X 2021-01-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33479212 Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Autism spectrum disorder (MTAG) at least 18,381 European ancestry cases, at least 27,969 European ancestry controls NA NR [NR] 9 autism spectrum disorder http://www.ebi.ac.uk/efo/EFO_0003756 GCST012092 Genome-wide genotyping array 2021-07-27 33479212 Yao X 2021-01-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33479212 Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Bipolar disorder (MTAG) at least 20,352 European ancestry cases, at least 31,358 European ancestry controls NA NR [NR] 54 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST012091 Genome-wide genotyping array 2021-07-27 33479212 Yao X 2021-01-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33479212 Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Major depressive disorder (MTAG) at least 170,756 European ancestry cases, at least 329,443 European ancestry controls NA NR [NR] 74 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST012090 Genome-wide genotyping array 2021-07-27 33479212 Yao X 2021-01-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33479212 Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Schizophrenia (MTAG) at least 33,640 European ancestry cases, at least 43,456 European ancestry controls NA NR [NR] 90 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST012089 Genome-wide genotyping array 2021-07-27 33479212 Yao X 2021-01-21 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/33479212 Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders. Neuropsychiatric disorders 19,099 European ancestry attention deficit hyperactivity disorder cases, 18,381 European ancestry autism spectrum disorder cases, 20,352 European ancestry bipolar disorder cases, 170,756 European ancestry major depressive disorder cases, 33,640 European ancestry schizophrenia cases, 466,420 European ancestry controls NA NR [NR] 43 attention deficit hyperactivity disorder, bipolar disorder, autism spectrum disorder, schizophrenia, major depressive disorder http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0002009 GCST012088 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort Fasting glucose in pregnancy (gestational week 14-16) 517 Scandinavian ancestry individuals NA Illumina [8717487] (imputed) 1 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007179 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort Fasting glucose in pregnancy (gestational week 30-32) 521 Scandinavian ancestry individuals NA Illumina [8709903] (imputed) 0 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007180 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort Two-hour glucose in pregnancy (gestational week 14-16) 506 Scandinavian ancestry individuals NA Illumina [8717487] (imputed) 0 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007181 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort Two-hour glucose in pregnancy (gestational week 30-32) 512 Scandinavian ancestry individuals NA Illumina [8709903] (imputed) 2 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007182 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort General glucose level in pregnancy (gestational week 14-16) 497 Scandinavian ancestry individuals NA Illumina [8717487] (imputed) 0 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007183 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort General glucose level in pregnancy (gestational week 30-32) 506 Scandinavian ancestry individuals NA Illumina [8709903] (imputed) 1 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007184 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort Timing of glucose curve peak in pregnancy (gestational week 14-16) 497 Scandinavian ancestry individuals NA Illumina [8717487] (imputed) 0 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007185 Genome-wide genotyping array 2019-02-19 30324795 Moen GH 2018-09-18 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/30324795 Genetic determinants of glucose levels in pregnancy: genetic risk scores analysis and GWAS in the Norwegian STORK cohort Timing of glucose curve peak in pregnancy (gestational week 30-32) 506 Scandinavian ancestry individuals NA Illumina [8709903] (imputed) 0 gestational blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0009698 GCST007186 Genome-wide genotyping array 2019-03-21 30325047 Gellert-Kristensen H 2018-10-16 Hepatology www.ncbi.nlm.nih.gov/pubmed/30325047 Identification and replication of six new loci associated with gallstone disease. Gallstone disease 14,940 British ancestry cases, 322,268 British ancestry controls 1,522 Danish ancestry cases, 18,266 Danish ancestry controls Affymetrix [784257] 1 cholelithiasis, gallstones http://www.ebi.ac.uk/efo/EFO_0004799, http://www.ebi.ac.uk/efo/EFO_0004210 GCST007364 Genome-wide genotyping array 2019-01-08 30172742 Hu Y 2018-08-30 Bone www.ncbi.nlm.nih.gov/pubmed/30172742 Identification of novel variants associated with osteoporosis, type 2 diabetes and potentially pleiotropic loci using pleiotropic cFDR method. Femoral neck bone mineral density or type 2 diabetes (pleiotropy) 53,236 European ancestry individuals with bone mineral density data, 26,676 European ancestry type 2 diabetes cases, 132,532 European ancestry controls NA NR [132735] 0 type 2 diabetes mellitus, femoral neck bone mineral density http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0007785 GCST006861 Genome-wide genotyping array 2019-07-31 31028280 Ierodiakonou D 2019-04-26 J Expo Sci Environ Epidemiol www.ncbi.nlm.nih.gov/pubmed/31028280 Pathway analysis of a genome-wide gene by air pollution interaction study in asthmatic children. Post-bronchodilator FEV1 x air pollution (CO) interaction in childhood asthma 522 European ancestry children NA Illumina [474792] 6 forced expiratory volume, traffic air pollution measurement http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0007908 GCST008272 Genome-wide genotyping array 2019-07-31 31028280 Ierodiakonou D 2019-04-26 J Expo Sci Environ Epidemiol www.ncbi.nlm.nih.gov/pubmed/31028280 Pathway analysis of a genome-wide gene by air pollution interaction study in asthmatic children. Post-bronchodilator FEV1 x air pollution (NO2) interaction in childhood asthma 522 European ancestry children 88 African-American children Illumina [474792] 6 forced expiratory volume, traffic air pollution measurement http://www.ebi.ac.uk/efo/EFO_0004314, http://www.ebi.ac.uk/efo/EFO_0007908 GCST008273 Genome-wide genotyping array 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. IgA levels 16,883 Icelandic ancestry individuals 2,151 Swedish ancestry individuals Illumina [21568490] (imputed) 15 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST008568 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. Composite immunoglobulin trait (IgA x IgG x IgM) 14,183 Icelandic ancestry individuals 2,146 Swedish ancestry individuals Illumina [21568490] (imputed) 2 serum immunoglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010127 GCST008569 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. Composite immunoglobulin trait (IgA x IgG/IgM) 14,183 Icelandic ancestry individuals 2,146 Swedish ancestry individuals Illumina [21568490] (imputed) 8 immunoglobulin isotype switching measurement http://www.ebi.ac.uk/efo/EFO_0010128 GCST008570 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. Composite immunoglobulin trait (IgA x IgG) 14,183 Icelandic ancestry individuals 2,146 Swedish ancestry individuals Illumina [21568490] (imputed) 1 immunoglobulin isotype switching measurement http://www.ebi.ac.uk/efo/EFO_0010128 GCST008571 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. Composite immunoglobulin trait (IgA/IgG) 14,183 Icelandic ancestry individuals 2,146 Swedish ancestry individuals Illumina [21568490] (imputed) 12 immunoglobulin isotype switching measurement http://www.ebi.ac.uk/efo/EFO_0010128 GCST008572 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. Composite immunoglobulin trait (IgA/IgM) 14,183 Icelandic ancestry individuals 2,146 Swedish ancestry individuals Illumina [21568490] (imputed) 9 immunoglobulin isotype switching measurement http://www.ebi.ac.uk/efo/EFO_0010128 GCST008573 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. Composite immunoglobulin trait (IgG/IgM) 14,183 Icelandic ancestry individuals 2,146 Swedish ancestry individuals Illumina [21568490] (imputed) 4 immunoglobulin isotype switching measurement http://www.ebi.ac.uk/efo/EFO_0010128 GCST008574 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. IgM levels 14,442 Icelandic ancestry individuals 2,157 Swedish ancestry individuals Illumina [21568490] (imputed) 13 serum IgM measurement http://www.ebi.ac.uk/efo/EFO_0004993 GCST008575 Genome-wide genotyping array, Genome-wide sequencing 2019-09-02 28628107 Jonsson S 2017-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/28628107 Identification of sequence variants influencing immunoglobulin levels. IgG levels 15,536 Icelandic ancestry individuals 2,158 Swedish ancestry individuals Illumina [21568490] (imputed) 8 serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0004565 GCST008576 Genome-wide genotyping array, Genome-wide sequencing 2018-10-19 30194396 Rafnar T 2018-09-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30194396 Variants associating with uterine leiomyoma highlight genetic background shared by various cancers and hormone-related traits. Uterine fibroids 16,595 European ancestry cases, 523,330 European ancestry controls NA Affymetrix, Illumina [43421991] (imputed) 53 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST006462 Genome-wide genotyping array 2019-08-07 31009812 Hung RJ 2019-04-19 J Thorac Oncol www.ncbi.nlm.nih.gov/pubmed/31009812 Lung Cancer Risk in Never Smokers of European Descent is Associated with Genetic Variation in the 5P15.33 TERT-CLPTM1L Region. Adenocarcinoma in never smokers 1,837 European ancestry cases, 5,355 European ancestry controls 672 European ancestry cases, 940 European ancestry controls Illumina [at least 517482] (imputed) 1 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST008375 Genome-wide genotyping array 2019-08-07 31009812 Hung RJ 2019-04-19 J Thorac Oncol www.ncbi.nlm.nih.gov/pubmed/31009812 Lung Cancer Risk in Never Smokers of European Descent is Associated with Genetic Variation in the 5P15.33 TERT-CLPTM1L Region. Lung cancer in never smokers 2,676 European ancestry cases, 5,355 European ancestry controls 960 European ancestry cases, 940 European ancestry controls Illumina [at least 517482] (imputed) 2 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST008376 Genome-wide genotyping array 2019-12-09 31379025 Sugier PE 2019-08-04 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/31379025 Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood. Asthma (time to childhood onset) in early life tobacco smoke exposure 3,187 European ancestry individuals NA Illumina [2110000] (imputed) 1 age of onset of childhood onset asthma http://purl.obolibrary.org/obo/OBA_2001015 GCST009236 Genome-wide genotyping array 2019-12-09 31379025 Sugier PE 2019-08-04 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/31379025 Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood. Asthma (childhood onset) 5,086 European ancestry individuals NA Illumina [2110000] (imputed) 1 childhood onset asthma http://purl.obolibrary.org/obo/MONDO_0005405 GCST009237 Genome-wide genotyping array 2019-12-09 31379025 Sugier PE 2019-08-04 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/31379025 Genome-wide interaction study of early-life smoking exposure on time-to-asthma onset in childhood. Asthma (time to childhood onset) x early life tobacco smoke interaction 3,187 European ancestry exposed individuals, 5,086 European ancestry unexposed individuals NA Illumina [2110000] (imputed) 4 age of onset of childhood onset asthma, environmental tobacco smoke exposure measurement http://purl.obolibrary.org/obo/OBA_2001015, http://www.ebi.ac.uk/efo/EFO_0008361 GCST009238 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Bioavailable testosterone levels 188,507 European ancestry women NA Affymetrix [16585745] (imputed) 180 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90012102 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Bioavailable testosterone levels 178,782 European ancestry men NA Affymetrix [16577424] (imputed) 125 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90012103 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Bioavailable testosterone levels 382,988 European ancestry individuals NA Affymetrix [16583148] (imputed) 147 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90012104 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Estradiol levels 206,927 European ancestry men NA Affymetrix [16582268] (imputed) 22 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90012105 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Sex hormone-binding globulin levels adjusted for BMI 188,908 European ancestry women NA Affymetrix [16585854] (imputed) 359 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90012106 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Sex hormone-binding globulin levels 189,473 European ancestry women NA Affymetrix [16585866] (imputed) 332 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90012107 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Sex hormone-binding globulin levels adjusted for BMI 180,094 European ancestry men NA Affymetrix [16582621] (imputed) 357 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90012108 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Sex hormone-binding globulin levels 180,726 European ancestry men NA Affymetrix [16582614] (imputed) 347 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90012109 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Sex hormone-binding globulin levels adjusted for BMI 368,929 European ancestry individuals NA Affymetrix [16582909] (imputed) 658 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90012110 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Sex hormone-binding globulin levels 370,125 European ancestry individuals NA Affymetrix [16582965] (imputed) 620 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90012111 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Total testosterone levels 230,454 European ancestry women NA Affymetrix [16580851] (imputed) 254 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90012112 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Total testosterone levels 194,453 European ancestry men NA Affymetrix [16577313] (imputed) 231 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90012113 Genome-wide genotyping array 2020-12-14 32042192 Ruth KS 2020-02-10 Nat Med www.ncbi.nlm.nih.gov/pubmed/32042192 Using human genetics to understand the disease impacts of testosterone in men and women. Total testosterone levels 425,097 European ancestry individuals NA Affymetrix [16578495] (imputed) 238 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90012114 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Dilated cardiomyopathy 5,521 cases, 397,323 controls NA Affymetrix, Illumina [up to 7736182] (imputed) 6 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST011210 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular ejection fraction 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 5 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST011209 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular mass to end-diastolic volume ratio 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 8 Left ventricular mass to end-diastolic volume ratio http://www.ebi.ac.uk/efo/EFO_0010556 GCST011208 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular mass 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 4 left ventricular mass http://www.ebi.ac.uk/efo/EFO_0009289 GCST011207 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular end-diastolic volume 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 4 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST011206 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular end-systolic volume 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 9 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST011198 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular global circumferential strain 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 10 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST011217 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular global radial strain 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 7 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST011216 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular global longitudinal strain 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 1 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST011215 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricle wall thickness 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 9 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST011214 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Hypertrophic cardiomyopathy (MTAG) 1,733 European ancestry cases, 6,628 European ancestry controls NA Illumina [6530233] (imputed) 16 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST011205 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Dilated cardiomyopathy (MTAG) 5,521 cases, 397,323 controls NA Affymetrix, Illumina [up to 7736182] (imputed) 13 dilated cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000407 GCST011202 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular ejection fraction (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 1 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST011204 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular mass to end-diastolic volume ratio (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 1 Left ventricular mass to end-diastolic volume ratio http://www.ebi.ac.uk/efo/EFO_0010556 GCST011213 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular mass (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 1 left ventricular mass http://www.ebi.ac.uk/efo/EFO_0009289 GCST011212 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular end-diastolic volume (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 3 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST011203 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular end-systolic volume (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 3 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST011197 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular global circumferential strain (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 1 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST011201 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular global radial strain (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 1 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST011200 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricular global longitudinal strain (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 1 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST011199 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Left ventricle wall thickness (MTAG) 19,260 European ancestry individuals NA Affymetrix [~ 9500000] (imputed) 0 heart function measurement http://www.ebi.ac.uk/efo/EFO_0004311 GCST011196 Genome-wide genotyping array 2021-03-05 33495596 Tadros R 2021-01-25 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33495596 Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect. Hypertrophic cardiomyopathy 1,733 European ancestry cases, 6,628 European ancestry controls 2,694 European ancestry cases, 47,486 European ancestry controls Illumina [6530233] (imputed) 15 hypertrophic cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000538 GCST011211 Genome-wide genotyping array 2021-03-22 33592630 Herrera-Rivero M 2021-02-16 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/33592630 Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism. Venous thromboembolism 964 European ancestry cases, 899 European ancestry controls NA Illumina [484621] 20 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST011359 Genome-wide genotyping array 2019-05-07 30993211 Nakatochi M 2019-04-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30993211 Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals. Serum uric acid levels 121,745 Japanese ancestry individuals at least 101,293 European ancestry individuals Illumina [5864938] (imputed) 42 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST007725 Genome-wide genotyping array 2019-05-08 30993211 Nakatochi M 2019-04-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30993211 Genome-wide meta-analysis identifies multiple novel loci associated with serum uric acid levels in Japanese individuals. Serum uric acid levels 121,745 Japanese ancestry individuals, at least 88,461 European ancestry individuals NA Illumina [1986983] (imputed) 71 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST007733 Genome-wide genotyping array 2019-08-01 31053729 Styrkarsdottir U 2019-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31053729 GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Femoral neck size 28,954 European ancestry individuals 9,383 European ancestry individuals, 6,351 East Asian ancestry individuals Illumina [33400000] (imputed) 2 femoral neck size http://www.ebi.ac.uk/efo/EFO_0010076 GCST008278 Genome-wide genotyping array, Genome-wide sequencing 2019-08-01 31053729 Styrkarsdottir U 2019-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31053729 GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Trochanter size 28,944 European ancestry individuals 8,065 European ancestry individuals, 5,711 East Asian ancestry individuals Illumina [33400000] (imputed) 4 trochanter size http://www.ebi.ac.uk/efo/EFO_0010074 GCST008279 Genome-wide genotyping array, Genome-wide sequencing 2019-08-01 31053729 Styrkarsdottir U 2019-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31053729 GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Intertrochanteric region size 28,936 European ancestry individuals 7,912 European ancestry individuals, 5,696 East Asian ancestry individuals Illumina [33400000] (imputed) 7 intertrochanteric region size http://www.ebi.ac.uk/efo/EFO_0010075 GCST008280 Genome-wide genotyping array, Genome-wide sequencing 2019-08-01 31053729 Styrkarsdottir U 2019-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31053729 GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Spine bone size 29,059 European ancestry individuals 14,932 European ancestry individuals, 6,345 East Asian ancestry individuals Illumina [33400000] (imputed) 9 spine bone size http://www.ebi.ac.uk/efo/EFO_0004508 GCST008282 Genome-wide genotyping array, Genome-wide sequencing 2019-08-01 31053729 Styrkarsdottir U 2019-05-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31053729 GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures. Hip bone size 28,900 European ancestry individuals 7,912 European ancestry individuals, 5,699 East Asian ancestry individuals Illumina [33400000] (imputed) 8 hip bone size http://www.ebi.ac.uk/efo/EFO_0004844 GCST008281 Genome-wide genotyping array, Genome-wide sequencing 2018-12-05 30289880 Qi G 2018-10-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30289880 Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. Lipid traits (pleiotropy) (HIPO component 1) 188,577 European ancestry individuals NA NR [1800000] 24 total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004612 GCST006666 Genome-wide genotyping array 2018-12-05 30289880 Qi G 2018-10-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30289880 Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. Lipid traits (pleiotropy) (HIPO component 2) 188,577 European ancestry individuals NA NR [1800000] 10 total cholesterol measurement, triglyceride measurement, low density lipoprotein cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004612 GCST006667 Genome-wide genotyping array 2018-12-05 30289880 Qi G 2018-10-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30289880 Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. Social science traits (pleiotropy) (HIPO component 1) up to 630,791 European ancestry individuals NA NR [2100000] 14 neuroticism measurement, wellbeing measurement, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0007869, http://www.ebi.ac.uk/efo/EFO_0007006 GCST006665 Genome-wide genotyping array 2018-12-05 30289880 Qi G 2018-10-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30289880 Heritability informed power optimization (HIPO) leads to enhanced detection of genetic associations across multiple traits. Psychiatric diseases (pleiotropy) (HIPO component 1) 4,949 autism cases, 2787 ADHD cases, 6,990 bipolar disorder cases, 9,227 depression cases, 9,379 schizophrenia cases, 27,888 controls NA NR [1050000] 1 attention deficit hyperactivity disorder, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090 GCST006668 Genome-wide genotyping array 2019-03-21 30649302 Ruth KS 2019-01-14 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30649302 Genome-wide association study of anti-Müllerian hormone levels in pre-menopausal women of late reproductive age and relationship with genetic determinants of reproductive lifespan. Anti-Mullerian hormone levels in pre-menopausal women of late reproductive age 3,344 European ancestry women NA Illumina [~ 8400000] (imputed) 10 anti-Mullerian hormone measurement http://www.ebi.ac.uk/efo/EFO_0004769 GCST007363 Genome-wide genotyping array 2019-03-19 30700811 Wigmore EM 2019-01-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30700811 Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP. Antidepressant treatment resistance (> 2 drugs prescribed) 250 European ancestry cases, 3,202 European ancestry controls, 109 cases, 668 controls NA NR [7120598] (imputed) 4 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST007355 Genome-wide genotyping array 2019-03-19 30700811 Wigmore EM 2019-01-31 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30700811 Genome-wide association study of antidepressant treatment resistance in a population-based cohort using health service prescription data and meta-analysis with GENDEP. Antidepressant treatment resistance (number of drugs prescribed) 3,452 European ancestry individuals NA NR [7395460] (imputed) 4 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST007356 Genome-wide genotyping array 2019-07-25 30367910 Levin AM 2018-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/30367910 Integrative approach identifies corticosteroid response variant in diverse populations with asthma. Asthma control x inhaled corticosteroid treatment interaction (2df) 244 African American individuals up to 1,366 African American individuals, up to 1,461 Latino ancestry individuals, up to 98 European ancestry individuals Affymetrix [574370] 1 asthma symptoms measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0010049, http://purl.obolibrary.org/obo/GO_0031960 GCST008230 Genome-wide genotyping array 2019-07-25 30367910 Levin AM 2018-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/30367910 Integrative approach identifies corticosteroid response variant in diverse populations with asthma. Asthma control x inhaled corticosteroid treatment interaction (1df) 244 African American individuals up to 1,366 African American individuals, up to 1,461 Latino ancestry individuals, up to 98 European ancestry individuals Affymetrix [574370] 0 asthma symptoms measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0010049, http://purl.obolibrary.org/obo/GO_0031960 GCST008229 Genome-wide genotyping array 2019-07-25 30367910 Levin AM 2018-10-24 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/30367910 Integrative approach identifies corticosteroid response variant in diverse populations with asthma. Asthma control 244 African American individuals up to 1,366 African American individuals, up to 1,461 Latino ancestry individuals, up to 98 European ancestry individuals Affymetrix [574370] 0 asthma symptoms measurement http://www.ebi.ac.uk/efo/EFO_0010049 GCST008228 Genome-wide genotyping array 2018-12-19 29852030 Lores-Motta L 2018-05-31 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/29852030 Association of Genetic Variants With Response to Anti-Vascular Endothelial Growth Factor Therapy in Age-Related Macular Degeneration. Response to anti-VEGF treatment in neovascular age-related macular degeneration (visual acuity) 678 European ancestry cases 1,380 European and unknown ancestry cases Illumina [6089769] (imputed) 0 visual acuity measurement, response to anti-vascular endothelial growth factor drug http://www.ebi.ac.uk/efo/EFO_0008385, http://www.ebi.ac.uk/efo/EFO_0009467 GCST006808 Genome-wide genotyping array 2019-03-05 30377885 Fujimori S 2018-10-30 Dig Dis Sci www.ncbi.nlm.nih.gov/pubmed/30377885 Bactericidal/Permeability-Increasing Fold-Containing Family B Member 4 May Be Associated with NSAID-Induced Enteropathy. Non-steroidal anti-inflammatory drug-induced enteropathy 16 Japanese ancestry severe injury cases, 123 Japanese ancestry mild and no injury treated controls NA Illumina [580461] 1 response to non-steroidal anti-inflammatory, small intestine enteropathy http://www.ebi.ac.uk/efo/EFO_0005533, http://www.ebi.ac.uk/efo/EFO_0009705 GCST007258 Genome-wide genotyping array 2018-07-11 29700475 Wray NR 2018-04-26 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29700475 Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. Depression 135,458 European ancestry cases, 344,901 European ancestry controls NA NR [9622763] (imputed) 44 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST005839 Genome-wide genotyping array 2018-08-10 29844224 Loomis SJ 2018-05-29 Diabetes www.ncbi.nlm.nih.gov/pubmed/29844224 Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study. Percent glycated albumin 7,647 European ancestry individuals, 2,104 Black individuals 1,304 European ancestry individuals, 608 Black individuals Affymetrix [NR] (imputed) 2 percent glycated albumin http://www.ebi.ac.uk/efo/EFO_0009304 GCST006057 Genome-wide genotyping array 2018-08-10 29844224 Loomis SJ 2018-05-29 Diabetes www.ncbi.nlm.nih.gov/pubmed/29844224 Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study. Total glycated albumin levels 7,647 European ancestry individuals, 2,104 Black individuals NA Affymetrix [NR] (imputed) 3 total glycated albumin http://www.ebi.ac.uk/efo/EFO_0009305 GCST006058 Genome-wide genotyping array 2018-08-10 29844224 Loomis SJ 2018-05-29 Diabetes www.ncbi.nlm.nih.gov/pubmed/29844224 Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study. Fasting blood glucose 7,647 European ancestry individuals, 2,104 Black individuals NA Affymetrix [NR] (imputed) 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST006059 Genome-wide genotyping array 2018-08-10 29844224 Loomis SJ 2018-05-29 Diabetes www.ncbi.nlm.nih.gov/pubmed/29844224 Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study. Hemoglobin A1c levels 7,647 European ancestry individuals, 2,104 Black individuals NA Affymetrix [NR] (imputed) 3 hemoglobin A1 measurement http://www.ebi.ac.uk/efo/EFO_0007629 GCST006060 Genome-wide genotyping array 2018-08-10 29844224 Loomis SJ 2018-05-29 Diabetes www.ncbi.nlm.nih.gov/pubmed/29844224 Genome-Wide Association Study of Serum Fructosamine and Glycated Albumin in Adults Without Diagnosed Diabetes: Results from the Atherosclerosis Risk in Communities Study. Fructosamine levels 7,647 European ancestry individuals, 2,104 Black individuals 1,304 European ancestry individuals, 608 Black individuals Affymetrix [NR] (imputed) 2 fructosamine measurement http://www.ebi.ac.uk/efo/EFO_0009303 GCST006056 Genome-wide genotyping array 2019-10-24 31099175 Wetherill L 2019-05-17 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/31099175 Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans. Alcohol or illicit drug dependence 2,927 European ancestry cases, 4,364 European ancestry controls, 1,315 African American cases, 1,817 African American controls 630 European ancestry cases, 1,020 European ancestry controls, 1,912 African American cases, 900 African American controls Illumina [NR] (imputed) 0 drug dependence http://www.ebi.ac.uk/efo/EFO_0003890 GCST008914 Genome-wide genotyping array 2019-05-17 31040861 Thomson RJ 2019-04-16 Front Genet www.ncbi.nlm.nih.gov/pubmed/31040861 New Genetic Loci Associated With Chronic Kidney Disease in an Indigenous Australian Population. Urinary albumin-to-creatinine ratio 249 Tiwi Islander (founder/genetic isolate) individuals 497 Tiwi Islander (founder/genetic isolate) individuals Affymetrix [NR] 0 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST007832 Genome-wide genotyping array 2019-09-24 31219150 Ekenberg C 2019-06-13 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/31219150 Single nucleotide polymorphisms in HLA alleles are associated with HIV-1 viral load in demographically diverse, ART-naïve participants from the START trial. Pre-treatment viral load in HIV-1 infection 1,398 European ancestry individuals, 572 Black individuals, 418 Hispanic individuals, 13 Asian ancestry individuals, 39 individuals NA Affymetrix [339439] 93 viral load http://www.ebi.ac.uk/efo/EFO_0010125 GCST008758 Genome-wide genotyping array 2019-05-20 31006500 Liu M 2019-04-04 Clin Nutr www.ncbi.nlm.nih.gov/pubmed/31006500 Protein and fat intake interacts with the haplotype of PTPN11_rs11066325, RPH3A_rs886477, and OAS3_rs2072134 to modulate serum HDL concentrations in middle-aged people. Low HDL-cholesterol levels 2,873 Korean ancestry cases, 5,966 Korean ancestry controls NA Affymetrix [NR] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007840 Genome-wide genotyping array 2019-08-05 31120506 Grassmann F 2019-05-23 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/31120506 Assessment of Novel Genome-Wide Significant Gene Loci and Lesion Growth in Geographic Atrophy Secondary to Age-Related Macular Degeneration. Geographic atrophy lesion growth rate in age-related macular degeneration 935 European ancestry individuals NA Affymetrix [7596219] (imputed) 3 geographic atrophy lesion growth http://www.ebi.ac.uk/efo/EFO_0010080 GCST008356 Genome-wide genotyping array 2019-06-13 31102405 Labreche K 2019-05-17 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/31102405 A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC network study. Primary central nervous system lymphoma 475 European ancestry cases, 1,134 European ancestry controls NA Illumina [> 10000000] (imputed) 7 central nervous system non-hodgkin lymphoma http://purl.obolibrary.org/obo/MONDO_0044887 GCST007896 Genome-wide genotyping array 2019-12-03 31387361 Fulmer D 2019-08-07 Circulation www.ncbi.nlm.nih.gov/pubmed/31387361 Defects in the Exocyst-Cilia Machinery Cause Bicuspid Aortic Valve Disease and Aortic Stenosis. Bicuspid aortic valve 452 European ancestry cases, 1,834 European ancestry controls 1,679 cases, 894 controls Illumina [1355128] 1 Bicuspid aortic valve http://purl.obolibrary.org/obo/HP_0001647 GCST009155 Genome-wide genotyping array 2020-02-20 31872970 Harvey PD 2019-12-24 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/31872970 Genome-wide association study of cognitive performance in U.S. veterans with schizophrenia or bipolar disorder. Cognitive performance in schizophrenia or bipolar disorder 1,095 European ancestry individuals with schizophrenia, 2,864 European ancestry individuals with bipolar disorder, 1,594 African Americans with schizophrenia, 1,007 African Americans with bipolar disorder NA Affymetrix [up to 6007810] (imputed) 1 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST009678 Genome-wide genotyping array 2020-03-06 31584380 Sun W 2019-10-04 Med Chem www.ncbi.nlm.nih.gov/pubmed/31584380 The Assessment of Interleukin-18 on the Risk of Coronary Heart Disease. Interleukin-18 levels 4,433 European ancestry individuals NA Illumina [up to 2543887] (imputed) 3 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST009736 Genome-wide genotyping array 2019-07-18 29185836 Chen MH 2017-11-29 Platelets www.ncbi.nlm.nih.gov/pubmed/29185836 Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation. Platelet aggregation 3,664 European ancestry individuals, 549 Old Order Amish (founder/genetic isolate) individuals 1,184 European ancestry individuals, 613 African American individuals Illumina [129094] 33 platelet aggregation http://purl.obolibrary.org/obo/GO_0070527 GCST008171 Exome genotyping array [Exome array] 2020-04-22 31932740 Bonomi A 2020-01-14 Genes Immun www.ncbi.nlm.nih.gov/pubmed/31932740 Analysis of the genetic variants associated with circulating levels of sgp130. Results from the IMPROVE study. Soluble gp130 levels 3,439 European ancestry individuals NA Illumina [360842] 2 soluble gp130 measurement http://www.ebi.ac.uk/efo/EFO_0010696 GCST009894 Targeted genotyping array [Cardio-MetaboChip, Immunochip] 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Apolipoprotein A1 levels 382,867 British ancestry individuals NA NR [NR] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90013843 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Apolipoprotein B levels 417,522 British ancestry individuals NA NR [NR] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90013844 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Total cholesterol levels 419,516 British ancestry individuals NA NR [NR] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90013845 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. High density lipoprotein cholesterol levels 384,986 British ancestry individuals NA NR [NR] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90013846 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Direct low density lipoprotein cholesterol levels 418,780 British ancestry individuals NA NR [NR] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90013847 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Lipoprotein (a) levels 334,646 British ancestry individuals NA NR [NR] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90013848 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Triglyceride levels 419,185 British ancestry individuals NA NR [NR] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90013849 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Non-HDL cholesterol levels 384,915 British ancestry individuals NA NR [NR] 0 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90013850 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Intermediate age-related macular degeneration 5,336 European ancestry cases, 14,590 European ancestry controls NA NR [NR] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90013851 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Age-related macular degeneration (choroidal neovascularisation) 8,544 European ancestry cases, 14,590 European ancestry controls NA NR [NR] (imputed) 0 wet macular degeneration http://www.ebi.ac.uk/efo/EFO_0004683 GCST90013852 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Age-related macular degeneration (geographic atrophy) 2,656 European ancestry cases, 14,590 European ancestry controls NA NR [NR] (imputed) 0 atrophic macular degeneration http://www.ebi.ac.uk/efo/EFO_1001492 GCST90013853 Genome-wide genotyping array 2021-03-09 33211829 Han X 2020-11-19 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/33211829 The effects of eight serum lipid biomarkers on age-related macular degeneration risk: a Mendelian randomization study. Advanced age-related macular degeneration 12,711 European ancestry cases, 14,590 European ancestry controls NA NR [NR] (imputed) 0 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90013854 Genome-wide genotyping array 2021-04-08 33665242 Wendt FR 2021-02-18 Neurobiol Stress www.ncbi.nlm.nih.gov/pubmed/33665242 Sex-stratified gene-by-environment genome-wide interaction study of trauma, posttraumatic-stress, and suicidality. Suicidality x trauma related phenotype interaction 123,633 European ancestry individuals 3,099 European ancestry individuals NR [7284651] (imputed) 0 suicide behaviour measurement, post-traumatic stress disorder, response to trauma exposure http://www.ebi.ac.uk/efo/EFO_0006882, http://www.ebi.ac.uk/efo/EFO_0001358, http://www.ebi.ac.uk/efo/EFO_0008483 GCST011459 Genome-wide genotyping array 2021-04-08 33665242 Wendt FR 2021-02-18 Neurobiol Stress www.ncbi.nlm.nih.gov/pubmed/33665242 Sex-stratified gene-by-environment genome-wide interaction study of trauma, posttraumatic-stress, and suicidality. Suicidality 123,633 European ancestry individuals 3,099 European ancestry individuals NR [7284651] (imputed) 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST011460 Genome-wide genotyping array 2020-11-24 31173346 Wang S 2019-06-27 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31173346 Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria. Breast cancer somatic mutation signature APOBEC C>T or C>G 974 European, African American and Asian ancestry individuals 170 Nigerian ancestry individuals Affymetrix [7177790] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010761 Genome-wide genotyping array 2020-11-24 31173346 Wang S 2019-06-27 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31173346 Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria. Breast cancer somatic mutation signature APOBEC C>T 974 European, African American and Asian ancestry individuals NA Affymetrix [7177790] (imputed) 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010760 Genome-wide genotyping array 2020-11-24 31173346 Wang S 2019-06-27 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31173346 Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria. Breast cancer somatic mutation signature APOBEC C>G 974 European, African American and Asian ancestry individuals NA Affymetrix [7177790] (imputed) 1 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010759 Genome-wide genotyping array 2020-11-24 31173346 Wang S 2019-06-27 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31173346 Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria. Breast cancer somatic mutation signature Aging 974 European, African American and Asian ancestry individuals NA Affymetrix [7177790] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010758 Genome-wide genotyping array 2020-11-24 31173346 Wang S 2019-06-27 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31173346 Germline variants and somatic mutation signatures of breast cancer across populations of African and European ancestry in the US and Nigeria. Breast cancer somatic mutation signature Homologous Recombination Deficiency 974 European, African American and Asian ancestry individuals NA Affymetrix [7177790] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST010757 Genome-wide genotyping array 2019-12-11 31073882 Plotnikov D 2019-05-09 Hum Genet www.ncbi.nlm.nih.gov/pubmed/31073882 A commonly occurring genetic variant within the NPLOC4-TSPAN10-PDE6G gene cluster is associated with the risk of strabismus. Strabismus 1,345 British ancestry cases, 65,349 British ancestry controls 116 cases, 5,084 controls Affymetrix [7469170] (imputed) 22 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST009247 Genome-wide genotyping array 2021-08-18 33657282 Liu X 2021-03-03 Aging Cell www.ncbi.nlm.nih.gov/pubmed/33657282 Integrated genetic analyses revealed novel human longevity loci and reduced risks of multiple diseases in a cohort study of 15,651 Chinese individuals. Longevity 11,045 Chinese ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 10 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST012210 Genome-wide genotyping array 2021-08-23 33674626 Yoon KJ 2021-03-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33674626 Variants in NEB and RIF1 genes on chr2q23 are associated with skeletal muscle index in Koreans: genome-wide association study. Skeletal muscle index 2,046 Korean ancestry individuals NA Illumina [6391983] (imputed) 1 muscle measurement http://www.ebi.ac.uk/efo/EFO_0004515 GCST012217 Genome-wide genotyping array 2021-04-22 33591409 Koskela M 2021-02-16 Pediatr Nephrol www.ncbi.nlm.nih.gov/pubmed/33591409 HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study. Inflammatory bowel disease 49 Finnish ancestry cases, 18,757 Finnish ancestry controls NA Illumina [NR] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST011538 Genome-wide genotyping array 2021-04-22 33591409 Koskela M 2021-02-16 Pediatr Nephrol www.ncbi.nlm.nih.gov/pubmed/33591409 HLA-DQ and HLA-DRB1 alleles associated with Henoch-Schönlein purpura nephritis in Finnish pediatric population: a genome-wide association study. Immunoglobulin A vasculitis 46 Finnish ancestry cases, 18,757 Finnish ancestry controls NA Illumina [NR] (imputed) 51 Henoch-Schoenlein purpura http://www.ebi.ac.uk/efo/EFO_1000965 GCST011537 Genome-wide genotyping array 2020-09-12 32469969 Pott J 2020-05-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/32469969 Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. Carotid plaque maximum area 727 European ancestry men, 550 European ancestry women NA Affymetrix [532676] (imputed) 14 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST010536 Genome-wide genotyping array 2020-09-12 32469969 Pott J 2020-05-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/32469969 Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. Sum of carotid plaque area 727 European ancestry men, 550 European ancestry women NA Affymetrix [532676] (imputed) 13 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST010538 Genome-wide genotyping array 2020-09-12 32469969 Pott J 2020-05-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/32469969 Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. Mean area of carotid plaque 727 European ancestry men, 550 European ancestry women NA Affymetrix [532676] (imputed) 9 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST010537 Genome-wide genotyping array 2020-09-12 32469969 Pott J 2020-05-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/32469969 Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. Maximum stenosis 727 European ancestry men, 550 European ancestry women NA Affymetrix [532676] (imputed) 13 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST010541 Genome-wide genotyping array 2020-09-12 32469969 Pott J 2020-05-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/32469969 Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. Mean degree of stenosis 727 European ancestry men, 550 European ancestry women NA Affymetrix [532676] (imputed) 11 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST010540 Genome-wide genotyping array 2020-09-12 32469969 Pott J 2020-05-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/32469969 Genome-wide analysis of carotid plaque burden suggests a role of IL5 in men. Sum of stenosis 727 European ancestry men, 550 European ancestry women NA Affymetrix [532676] (imputed) 11 carotid plaque build http://www.ebi.ac.uk/efo/EFO_0006501 GCST010539 Genome-wide genotyping array 2019-03-14 23544012 Gaudet MM 2013-03-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23544012 Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk. Breast cancer in BRCA2 mutation carriers 4,330 European ancestry affected women, 3,881 European ancestry unaffected women NA Illumina [at least 200908] (imputed) 5 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST007302 Targeted genotyping array [iCOGS] 2020-04-17 31958309 Hsieh AR 2020-01-01 BMJ Open Diabetes Res Care www.ncbi.nlm.nih.gov/pubmed/31958309 Lack of association of genetic variants for diabetic retinopathy in Taiwanese patients with diabetic nephropathy. Diabetic retinopathy in type 2 diabetes 206 East Asian ancestry cases, 206 East Asian ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST009840 Genome-wide genotyping array 2022-05-30 35184318 Li Y 2022-02-19 Hepatology www.ncbi.nlm.nih.gov/pubmed/35184318 Genome-wide Meta-analysis Identifies Novel Susceptibility Loci for Autoimmune Hepatitis Type 1. Autoimmune hepatitis type-1 1,622 Han Chinese ancestry cases, 10,466 Han Chinese ancestry controls NA Illumina [660000] (imputed) 8 Autoimmune Hepatitis http://www.ebi.ac.uk/efo/EFO_0005676 GCST90103934 Genome-wide genotyping array 2021-09-02 33654129 Jung HU 2021-03-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33654129 Identification of genetic loci affecting body mass index through interaction with multiple environmental factors using structured linear mixed model. BMI x environmental factors (including physical activity) interaction 8,155 Korean ancestry individuals NA Affymetrix [5908111] (imputed) 7 household income, smoking status measurement, educational attainment, protein intake measurement, carbohydrate intake measurement, alcohol consumption measurement, physical activity measurement, body mass index, energy intake measurement http://www.ebi.ac.uk/efo/EFO_0009695, http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0011015, http://www.ebi.ac.uk/efo/EFO_0010810, http://www.ebi.ac.uk/efo/EFO_0010811, http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0008002, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0009374 GCST012283 Genome-wide genotyping array 2021-09-02 33654129 Jung HU 2021-03-02 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33654129 Identification of genetic loci affecting body mass index through interaction with multiple environmental factors using structured linear mixed model. BMI x environmental factors (excluding physical activity) interaction 8,155 Korean ancestry individuals NA Affymetrix [5908111] (imputed) 11 household income, smoking status measurement, educational attainment, protein intake measurement, carbohydrate intake measurement, alcohol consumption measurement, body mass index, energy intake measurement http://www.ebi.ac.uk/efo/EFO_0009695, http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0011015, http://www.ebi.ac.uk/efo/EFO_0010810, http://www.ebi.ac.uk/efo/EFO_0010811, http://www.ebi.ac.uk/efo/EFO_0007878, http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0009374 GCST012282 Genome-wide genotyping array 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. LDL cholesterol levels 13,890 Korean ancestry individuals NA Illumina [240075] 6 LDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007804 GCST011018 Exome genotyping array [Exome array] 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. Triglyceride levels 13,890 Korean ancestry individuals NA Illumina [240075] 6 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST011017 Exome genotyping array [Exome array] 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. Total cholesterol levels 13,890 Korean ancestry individuals NA Illumina [240075] 8 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST011016 Exome genotyping array [Exome array] 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. Hypertriglyceridemia 13,890 Korean ancestry individuals NA Illumina [240075] 1 Hypertriglyceridemia http://www.ebi.ac.uk/efo/EFO_0004211 GCST011015 Exome genotyping array [Exome array] 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. Hyper-LDL-cholesterolemia 13,890 Korean ancestry individuals NA Illumina [240075] 0 familial hypercholesterolemia http://www.ebi.ac.uk/efo/EFO_0004911 GCST011014 Exome genotyping array [Exome array] 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. Hypo-HDL-cholesterolemia 13,890 Korean ancestry individuals NA Illumina [240075] 1 Hypocholesterolemia http://purl.obolibrary.org/obo/HP_0003146 GCST011013 Exome genotyping array [Exome array] 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. Dyslipidemia 13,890 Korean ancestry individuals NA Illumina [240075] 0 Rare dyslipidemia http://www.orpha.net/ORDO/Orphanet_101953 GCST011012 Exome genotyping array [Exome array] 2021-01-28 31087446 Han S 2019-05-13 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/31087446 Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups. HDL cholesterol levels 13,890 Korean ancestry individuals NA Illumina [240075] 7 HDL cholesterol change measurement http://www.ebi.ac.uk/efo/EFO_0007805 GCST011019 Exome genotyping array [Exome array] 2022-01-24 30026463 Sahibdeen V 2018-07-19 Nutr Diabetes www.ncbi.nlm.nih.gov/pubmed/30026463 Genetic variants in SEC16B are associated with body composition in black South Africans. Body composition traits 1,421 South African ancestry females, 505 South African ancestry males NA Illumina [125878] 10 body composition measurement http://www.ebi.ac.uk/efo/EFO_0005106 GCST012676 Targeted genotyping array [Metabochip] 2021-04-15 33568662 Dashti HS 2021-02-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/33568662 Genetic determinants of daytime napping and effects on cardiometabolic health. Daytime nap 452,633 European ancestry individuals 541,333 European ancestry individuals Affymetrix [13304133] (imputed) 106 daytime rest measurement http://www.ebi.ac.uk/efo/EFO_0007828 GCST011494 Genome-wide genotyping array 2021-05-27 33137338 Gorski M 2020-10-30 Kidney Int www.ncbi.nlm.nih.gov/pubmed/33137338 Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Estimated glomerular filtration rate (creatinine, Rapid3) 34,874 European, African American, Hispanic or South Asian cases, 107,090 European, African American, Hispanic or South Asian controls NA Affymetrix, Illumina [> 8000000] (imputed) 2 glomerular filtration rate, creatine measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0010472 GCST011749 Genome-wide genotyping array 2021-05-27 33137338 Gorski M 2020-10-30 Kidney Int www.ncbi.nlm.nih.gov/pubmed/33137338 Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Estimated glomerular filtration rate (creatinine, CKDi25) 19,901 European, African American or Hispanic cases, 175,244 European, African American or Hispanic controls NA Affymetrix, Illumina [> 8000000] (imputed) 4 glomerular filtration rate, creatine measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0010472 GCST011748 Genome-wide genotyping array 2021-05-27 33137338 Gorski M 2020-10-30 Kidney Int www.ncbi.nlm.nih.gov/pubmed/33137338 Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Estimated glomerular filtration rate (creatinine, Rapid3) 31,101 European ancestry cases, 102,485 European ancestry controls NA Affymetrix, Illumina [> 8000000] (imputed) 2 glomerular filtration rate, creatine measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0010472 GCST011747 Genome-wide genotyping array 2021-05-27 33137338 Gorski M 2020-10-30 Kidney Int www.ncbi.nlm.nih.gov/pubmed/33137338 Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Estimated glomerular filtration rate (creatinine, CKDi25) 19,419 European ancestry cases, 169,087 European ancestry controls NA Affymetrix, Illumina [> 8000000] (imputed) 3 glomerular filtration rate, creatine measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0010472 GCST011746 Genome-wide genotyping array 2021-05-27 33137338 Gorski M 2020-10-30 Kidney Int www.ncbi.nlm.nih.gov/pubmed/33137338 Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Estimated glomerular filtration rate (creatinine, Rapid3) 2,356 African American ancestry cases, 2,375 African American ancestry controls NA Affymetrix, Illumina [> 8000000] (imputed) 0 glomerular filtration rate, creatine measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0010472 GCST011745 Genome-wide genotyping array 2021-05-27 33137338 Gorski M 2020-10-30 Kidney Int www.ncbi.nlm.nih.gov/pubmed/33137338 Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Estimated glomerular filtration rate (creatinine, CKDi25) 374 African American ancestry cases, 4,183 African American ancestry controls NA Affymetrix, Illumina [> 8000000] (imputed) 0 glomerular filtration rate, creatine measurement http://www.ebi.ac.uk/efo/EFO_0005208, http://www.ebi.ac.uk/efo/EFO_0010472 GCST011744 Genome-wide genotyping array 2021-06-11 33225922 Adebamowo SN 2020-11-23 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/33225922 Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection. Cervical high-risk human papilloma virus infection (persistent) 51 Nigerian ancestry cases, 355 Nigerian ancestry controls NA Illumina [~ 18000000] (imputed) 8 human papilloma virus infection http://www.ebi.ac.uk/efo/EFO_0001668 GCST011836 Genome-wide genotyping array 2021-06-11 33225922 Adebamowo SN 2020-11-23 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/33225922 Genome-wide association study of prevalent and persistent cervical high-risk human papillomavirus (HPV) infection. Cervical high-risk human papilloma virus infection 125 Nigerian ancestry cases, 392 Nigerian ancestry controls NA Illumina [~ 18000000] (imputed) 11 human papilloma virus infection http://www.ebi.ac.uk/efo/EFO_0001668 GCST011837 Genome-wide genotyping array 2021-02-12 31376382 Yang C 2019-07-31 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/31376382 Exome-Wide Rare Loss-of-Function Variant Enrichment Study of 21,347 Han Chinese Individuals Identifies Four Susceptibility Genes for Psoriasis. Psoriasis 10,668 Chinese ancestry cases, 10,679 Chinese ancestry controls NA NR [66000] 6 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST011109 Exome genotyping array [Exome array] 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. B cell lymphocyte profile difference (1 day post influenza vaccination) 298 individuals NA NR [1665663] 1 lymphocyte count, response to vaccine http://www.ebi.ac.uk/efo/EFO_0004587, http://www.ebi.ac.uk/efo/EFO_0004645 GCST011885 Genome-wide genotyping array 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. B cell lymphocyte profile difference (7 days post influenza vaccination) 298 individuals NA NR [1665663] 5 lymphocyte count, response to vaccine http://www.ebi.ac.uk/efo/EFO_0004587, http://www.ebi.ac.uk/efo/EFO_0004645 GCST011884 Genome-wide genotyping array 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. B cell lymphocyte profile difference (90 days post influenza vaccination) 298 individuals NA NR [1665663] 2 lymphocyte count, response to vaccine http://www.ebi.ac.uk/efo/EFO_0004587, http://www.ebi.ac.uk/efo/EFO_0004645 GCST011883 Genome-wide genotyping array 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. T cell lymphocyte profile difference 298 individuals NA NR [1665663] 16 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST011882 Genome-wide genotyping array 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. T cell lymphocyte profile difference (1 day post influenza vaccination) 298 individuals NA NR [1665663] 1 lymphocyte count, response to vaccine http://www.ebi.ac.uk/efo/EFO_0004587, http://www.ebi.ac.uk/efo/EFO_0004645 GCST011881 Genome-wide genotyping array 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. T cell lymphocyte profile difference (7 days post influenza vaccination) 298 individuals NA NR [1665663] 1 lymphocyte count, response to vaccine http://www.ebi.ac.uk/efo/EFO_0004587, http://www.ebi.ac.uk/efo/EFO_0004645 GCST011880 Genome-wide genotyping array 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. T cell lymphocyte profile difference (90 days post influenza vaccination) 298 individuals NA NR [1665663] 3 lymphocyte count, response to vaccine http://www.ebi.ac.uk/efo/EFO_0004587, http://www.ebi.ac.uk/efo/EFO_0004645 GCST011879 Genome-wide genotyping array 2021-06-14 33230199 Okada D 2020-11-23 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/33230199 Genome-wide association study of individual differences of human lymphocyte profiles using large-scale cytometry data. B cell lymphocyte profile difference 298 individuals NA NR [1665663] 3 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST011886 Genome-wide genotyping array 2021-08-26 33710309 Shadrina AS 2021-03-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33710309 Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function. IgG galactosylation phenotypes (multivariate analysis) 8,090 European ancestry individuals 3,147 European ancestry individuals NR [NR] (imputed) 0 IgG galactosylation measurement http://www.ebi.ac.uk/efo/EFO_0008425 GCST012250 Genome-wide genotyping array 2021-08-26 33710309 Shadrina AS 2021-03-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33710309 Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function. IgG bisecting N-acetyl glucosamine phenotypes (multivariate analysis) 8,090 European ancestry individuals 3,147 European ancestry individuals NR [NR] (imputed) 1 IgG bisecting N-acetyl glucosamine measurement http://www.ebi.ac.uk/efo/EFO_0008426 GCST012249 Genome-wide genotyping array 2021-08-26 33710309 Shadrina AS 2021-03-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33710309 Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function. IgG N-glycosylation phenotypes (multivariate analysis) 8,090 European ancestry individuals 3,147 European ancestry individuals NR [NR] (imputed) 2 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST012248 Genome-wide genotyping array 2021-08-26 33710309 Shadrina AS 2021-03-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33710309 Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function. IgG fucosylation phenotypes (multivariate analysis) 8,090 European ancestry individuals 3,147 European ancestry individuals NR [NR] (imputed) 0 IgG fucosylation measurement http://www.ebi.ac.uk/efo/EFO_0008427 GCST012247 Genome-wide genotyping array 2021-08-26 33710309 Shadrina AS 2021-03-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/33710309 Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function. IgG sialylation phenotypes (multivariate analysis) 8,090 European ancestry individuals 3,147 European ancestry individuals NR [NR] (imputed) 0 IgG sialylation measurement http://www.ebi.ac.uk/efo/EFO_0008428 GCST012246 Genome-wide genotyping array 2021-04-30 32258092 Xu Y 2020-03-11 Int J Genomics www.ncbi.nlm.nih.gov/pubmed/32258092 A Pooling Genome-Wide Association Study Identifies Susceptibility Loci and Signaling Pathways of Immune Thrombocytopenia in Chinese Han Population. Immune thrombocytopenia 200 Han Chinese ancestry cases, 200 Han Chinese ancestry controls 250 Han Chinese ancestry cases, 250 Han Chinese ancestry controls Illumina [862620] 0 autoimmune thrombocytopenic purpura http://www.ebi.ac.uk/efo/EFO_0007160 GCST011588 Genome-wide genotyping array 2021-08-02 33126880 Chang X 2020-10-30 Nutr J www.ncbi.nlm.nih.gov/pubmed/33126880 Effect of plasma polyunsaturated fatty acid levels on leukocyte telomere lengths in the Singaporean Chinese population. Telomere length x n-3 polyunsaturated fatty acid level interaction 1,349 Chinese ancestry individuals NA Illumina [NR] (imputed) 1 polyunsaturated fatty acid measurement, telomere length http://www.ebi.ac.uk/efo/EFO_0010733, http://www.ebi.ac.uk/efo/EFO_0004505 GCST90013430 Genome-wide genotyping array 2019-07-30 31003110 Kim S 2019-04-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/31003110 Heritability estimates of individual psychological distress symptoms from genetic variation. Psychological wellbeing index 1 (lack of subjective wellbeing and health) up to 12,680 Korean ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 13 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST008262 Genome-wide genotyping array 2019-07-30 31003110 Kim S 2019-04-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/31003110 Heritability estimates of individual psychological distress symptoms from genetic variation. Psychological wellbeing index 3 (fatigue and loss of appetite) up to 12,680 Korean ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 27 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST008263 Genome-wide genotyping array 2019-07-30 31003110 Kim S 2019-04-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/31003110 Heritability estimates of individual psychological distress symptoms from genetic variation. Psychological wellbeing index 12 (lack of enjoying daily life) up to 12,680 Korean ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 6 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST008264 Genome-wide genotyping array 2019-07-30 31003110 Kim S 2019-04-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/31003110 Heritability estimates of individual psychological distress symptoms from genetic variation. Psychological wellbeing (social role performance and self-confidence) up to 12,680 Korean ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 9 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST008265 Genome-wide genotyping array 2019-07-30 31003110 Kim S 2019-04-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/31003110 Heritability estimates of individual psychological distress symptoms from genetic variation. Psychological wellbeing (depressiveness) up to 12,680 Korean ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 11 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST008261 Genome-wide genotyping array 2019-07-30 31003110 Kim S 2019-04-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/31003110 Heritability estimates of individual psychological distress symptoms from genetic variation. Psychological wellbeing (health and vitality) up to 12,680 Korean ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 24 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST008266 Genome-wide genotyping array 2019-07-30 31003110 Kim S 2019-04-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/31003110 Heritability estimates of individual psychological distress symptoms from genetic variation. Psychological wellbeing index (total score) up to 12,680 Korean ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 17 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST008267 Genome-wide genotyping array 2019-08-01 30992453 Bjornsdottir G 2019-04-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30992453 A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy. Sural nerve amplitude potential 6,879 Icelandic ancestry individuals NA Illumina [at least 37600000] (imputed) 1 nerve conduction amplitude http://www.ebi.ac.uk/efo/EFO_0010070 GCST008312 Genome-wide genotyping array, Genome-wide sequencing 2019-08-01 30992453 Bjornsdottir G 2019-04-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30992453 A PRPH splice-donor variant associates with reduced sural nerve amplitude and risk of peripheral neuropathy. Sural nerve conduction velocity 6,979 Icelandic ancestry individuals NA Illumina [37600000] (imputed) 0 nerve conduction velocity http://www.ebi.ac.uk/efo/EFO_0010069 GCST008313 Genome-wide genotyping array, Genome-wide sequencing 2019-08-12 31213470 Moon JY 2019-06-18 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/31213470 A Genome-Wide Association Study Identifies Blood Disorder-Related Variants Influencing Hemoglobin A1c With Implications for Glycemic Status in U.S. Hispanics/Latinos. Glycated hemoglobin levels 9,636 Hispanic/Latino individuals 4,777 Hispanic/Latino individuals Illumina [11510031] (imputed) 16 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST008398 Genome-wide genotyping array 2019-08-28 31206233 Real LM 2019-06-17 Liver Int www.ncbi.nlm.nih.gov/pubmed/31206233 A genome-wide association study in low susceptibility to hepatitis C virus infection (GEHEP012 Study). Low susceptibility to hepatitis C infection 27 Spanish ancestry uninfected high-risk individuals, 804 Spanish ancestry infected individuals NA Affymetrix [7675561] (imputed) 13 decreased susceptibility to hepatitis C infection http://www.ebi.ac.uk/efo/EFO_0010101 GCST008502 Genome-wide genotyping array 2018-05-11 29617998 Gao XR 2018-03-28 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/29617998 Genome-Wide Association Analyses Identify New Loci Influencing Intraocular Pressure. Intraocular pressure 115,486 European ancestry individuals NA Affymetrix [~ 11900000] (imputed) 320 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST005580 Genome-wide genotyping array 2018-09-19 29695241 Charmet R 2018-04-25 Cardiovasc Diabetol www.ncbi.nlm.nih.gov/pubmed/29695241 Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes. Coronary artery disease in type 1 diabetes 434 European ancestry cases with coronary artery disease, 3,123 European ancestry cases without coronary artery disease 585 cases with coronary artery disease, 2,612 cases without coronary artery disease Illumina [6728637] (imputed) 21 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST006281 Genome-wide genotyping array 2019-10-17 28989979 Howard DM 2017-08-10 Wellcome Open Res www.ncbi.nlm.nih.gov/pubmed/28989979 Haplotype-based association analysis of general cognitive ability in Generation Scotland, the English Longitudinal Study of Ageing, and UK Biobank. General cognitive ability 19,326 European ancestry individuals from up to 4,933 families 28,676 European ancestry individuals Illumina [at least 561125] (imputed) 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST008861 Genome-wide genotyping array 2019-05-10 30692689 Schork AJ 2019-01-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/30692689 A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment. Mental disorder 46,008 Danish ancestry cases, 19,526 Danish ancestry controls 4,481 cases, 2,682 controls Illumina [8018013] (imputed) 0 attention deficit hyperactivity disorder, bipolar disorder, autism spectrum disorder, mental or behavioural disorder, schizophrenia, mood disorder, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756, http://www.ebi.ac.uk/efo/EFO_0000677, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0004247, http://purl.obolibrary.org/obo/MONDO_0005351 GCST007777 Genome-wide genotyping array 2019-06-03 31015462 Graham SE 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015462 Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Estimated glomerular filtration rate 206,856 European ancestry individuals, 143,658 East Asian ancestry individuals NA Illumina [26237160] (imputed) 147 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST007876 Genome-wide genotyping array 2019-06-03 31015462 Graham SE 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015462 Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Creatinine levels 69,591 European ancestry individuals NA Illumina [24961484] (imputed) 25 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST007877 Genome-wide genotyping array 2019-06-03 31015462 Graham SE 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015462 Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Urea levels 20,700 European ancestry individuals NA Illumina [24961484] (imputed) 4 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST007878 Genome-wide genotyping array 2019-06-03 31015462 Graham SE 2019-04-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31015462 Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. Chronic kidney disease 2,044 European ancestry cases, 65,575 European ancestry controls NA Illumina [24961484] (imputed) 3 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST007879 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at birth 9,286 Norwegian ancestry individuals 5,235 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009282 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 6 weeks old 6,450 Norwegian ancestry individuals 3,444 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009288 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 3 months old 7,970 Norwegian ancestry individuals 4,454 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009290 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 6 months old 8,017 Norwegian ancestry individuals 4,516 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009291 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 8 months old 7,197 Norwegian ancestry individuals 3,966 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009293 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 1 year old 6,970 Norwegian ancestry individuals 3,839 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 3 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009294 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 1.5 years old 6,800 Norwegian ancestry individuals 3,780 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009295 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 2 years old 4,631 Norwegian ancestry individuals 2,501 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009296 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 3 years old 5,069 Norwegian ancestry individuals 2,833 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009297 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 5 years old 4,245 Norwegian ancestry individuals 2,209 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009298 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 7 years old 4,629 Norwegian ancestry individuals 2,638 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009299 Genome-wide genotyping array 2019-12-16 31575865 Helgeland O 2019-10-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/31575865 Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth. BMI at 8 years old 3,862 Norwegian ancestry individuals 2,087 Norwegian ancestry individuals Illumina [~ 8500000] (imputed) 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST009300 Genome-wide genotyping array 2019-08-12 31212010 Cabana-Dominguez J 2019-06-15 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/31212010 Genome-wide association meta-analysis of cocaine dependence: Shared genetics with comorbid conditions. Cocaine dependence 2,085 European ancestry cases, 4,293 European ancestry controls NA Illumina [9290362] (imputed) 21 cocaine dependence http://www.ebi.ac.uk/efo/EFO_0002610 GCST008399 Genome-wide genotyping array 2019-03-28 30738427 Penney ME 2019-02-09 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/30738427 A genome-wide association study identifies single nucleotide polymorphisms associated with time-to-metastasis in colorectal cancer. Metastasis in stage I-III microsatellite instability low/stable colorectal cancer (time to event) 379 European ancestry cases NA Illumina [810622] 26 metastasis measurement, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0007675, http://www.ebi.ac.uk/efo/EFO_0008336 GCST007434 Genome-wide genotyping array 2019-08-16 31211820 Deek R 2019-06-18 PLoS One www.ncbi.nlm.nih.gov/pubmed/31211820 Genome-wide association analysis of HDL-C in a Lebanese cohort. High density lipoprotein cholesterol levels 2,700 Lebanese ancestry individuals NA Illumina [307238] 10 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST008444 Genome-wide genotyping array 2019-10-29 31578528 Tin A 2019-10-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31578528 Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Urate levels 288,649 European ancestry individuals, 125,725 East Asian ancestry individuals, 33,671 African American individuals, 9,037 South Asian ancestry individuals, 608 Hispanic individuals NA Affymetrix, Illumina [8249849] (imputed) 267 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST008972 Genome-wide genotyping array 2019-10-29 31578528 Tin A 2019-10-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31578528 Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Urate levels 288,649 European ancestry individuals NA Affymetrix, Illumina [8217339] (imputed) 154 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST008971 Genome-wide genotyping array 2019-10-29 31578528 Tin A 2019-10-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31578528 Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Urate levels 174,111 European, East Asian, African American, South Asian and Hispanic ancestry men, 172,102 European, East Asian, African American, South Asian and Hispanic ancestry women NA Affymetrix, Illumina [8249849] (imputed) 176 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST008973 Genome-wide genotyping array 2019-10-29 31578528 Tin A 2019-10-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/31578528 Target genes, variants, tissues and transcriptional pathways influencing human serum urate levels. Gout 13,179 European, African American and unknown ancestry cases, 750,634 European, African American and unknown ancestry controls NA Affymetrix, Illumina [8249849] (imputed) 7 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST008970 Genome-wide genotyping array 2019-09-12 31383772 Yan C 2019-08-05 Gut www.ncbi.nlm.nih.gov/pubmed/31383772 Meta-analysis of genome-wide association studies and functional assays decipher susceptibility genes for gastric cancer in Chinese populations. Gastric cancer 3,771 Chinese ancestry cases, 5,426 Chinese ancestry controls 7,035 Chinese ancestry cases, 8,323 Chinese ancestry controls Affymetrix, Illumina [6192596] (imputed) 6 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST008646 Genome-wide genotyping array 2019-06-14 31109976 Suvichapanich S 2019-05-20 Antimicrob Agents Chemother www.ncbi.nlm.nih.gov/pubmed/31109976 Genome-Wide Association Study Confirming the Association of NAT2 with Susceptibility to Anti-tuberculosis Drug-Induced Liver Injury in Thai Patients. Liver injury in anti-tuberculosis drug treatment 79 Thai ancestry cases, 239 Thai ancestry controls NA Illumina [545492] 2 response to anti-tuberculosis drug, tuberculosis, drug-induced liver injury http://www.ebi.ac.uk/efo/EFO_0007918, http://purl.obolibrary.org/obo/MONDO_0018076, http://www.ebi.ac.uk/efo/EFO_0004228 GCST007897 Genome-wide genotyping array 2019-06-27 31118946 Jiao H 2019-05-01 Front Genet www.ncbi.nlm.nih.gov/pubmed/31118946 Genome-Wide Interaction and Pathway Association Studies for Body Mass Index. Obesity (extreme) (SNP x SNP interaction) 493 European ancestry female cases, 537 European ancestry female controls NA Illumina [497174] 39 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST007997 Genome-wide genotyping array 2020-06-16 23394302 Pechlivanis S 2013-02-08 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/23394302 Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study. Coronary artery calcification 2,158 Europen ancestry males, 2,171 European ancestry females NA Illumina [up to 196725] 4 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST010078 Targeted genotyping array [Metabochip] 2018-11-02 30218097 Munz M 2018-09-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30218097 Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci. Periodontitis 4,102 European ancestry cases, 8,489 European ancestry controls 993 European ancestry cases, 1,419 European ancestry controls Affymetrix, Illumina [1722107] (imputed) 12 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST006486 Genome-wide genotyping array 2018-12-06 30277614 Carlson JC 2018-09-11 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30277614 Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts. Nonsyndromic cleft lip with or without cleft palate x sex interaction (2df test) 1,293 male cases, 849 female cases, 713 male controls, 987 female controls NA Illumina [up to 34985077] (imputed) 3 Cleft palate, sex interaction measurement, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0003959 GCST006680 Genome-wide genotyping array 2018-11-12 30273415 Hatzikotoulas K 2018-05-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30273415 Genome-wide association study of developmental dysplasia of the hip identifies an association with GDF5. Developmental dysplasia of the hip 770 European ancestry cases, 3,364 European ancestry controls 1,129 European ancestry cases, 4,652 European ancestry controls Illumina [256867] 3 developmental dysplasia of the hip http://www.ebi.ac.uk/efo/EFO_1000648 GCST006566 Genome-wide genotyping array 2019-01-25 30087447 Aubart M 2018-08-07 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30087447 Association of modifiers and other genetic factors explain Marfan syndrome clinical variability. Severe aortic features in Marfan syndrome 51 European ancestry cases, 47 European ancestry controls NA Illumina [at least 701570] (imputed) 4 thoracic aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0004282 GCST006957 Genome-wide genotyping array 2018-09-19 30079052 Rujescu D 2018-07-20 Front Neurol www.ncbi.nlm.nih.gov/pubmed/30079052 Genome-Wide Association Study in Vestibular Neuritis: Involvement of the Host Factor for HSV-1 Replication. Vestibular neuritis 131 European ancestry cases, 2,609 German ancestry controls NA Affymetrix, Illumina [7813927] (imputed) 4 vestibular neuronitis http://www.ebi.ac.uk/efo/EFO_0007537 GCST006275 Genome-wide genotyping array 2018-10-17 30116032 Erlangsen A 2018-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30116032 Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study. Affective disorder and suicide attempts 4,302 European ancestry cases, 13,294 European ancestry population controls NA Illumina [11601089] (imputed) 7 attempted suicide, mood disorder http://www.ebi.ac.uk/efo/EFO_0004321, http://www.ebi.ac.uk/efo/EFO_0004247 GCST006420 Genome-wide genotyping array 2018-10-17 30116032 Erlangsen A 2018-08-16 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30116032 Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study. Suicide attempts 6,024 European ancestry cases, 44,240 European ancestry controls NA Illumina [11601089] (imputed) 10 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST006419 Genome-wide genotyping array 2018-10-17 30089514 Chen JA 2018-08-08 Mol Neurodegener www.ncbi.nlm.nih.gov/pubmed/30089514 Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases. Progressive supranuclear palsy 1,646 European ancestry cases, 10,662 European ancestry controls NA Illumina [6419662] (imputed) 13 progressive supranuclear palsy http://purl.obolibrary.org/obo/MONDO_0019037 GCST006418 Genome-wide genotyping array 2019-01-30 30647433 Legge SE 2019-01-15 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30647433 A genome-wide association study in individuals of African ancestry reveals the importance of the Duffy-null genotype in the assessment of clozapine-related neutropenia. Neutrophil level response to clozapine in treatment-resistant schizophrenia 552 Sub-Saharan African ancestry individuals NA Illumina [~ 13500000] (imputed) 2 neutrophil count, response to clozapine http://www.ebi.ac.uk/efo/EFO_0004833, http://purl.obolibrary.org/obo/GO_0097338 GCST006987 Genome-wide genotyping array 2018-11-09 30271932 Oskarsson GR 2018-05-17 Commun Biol www.ncbi.nlm.nih.gov/pubmed/30271932 A truncating mutation in EPOR leads to hypo-responsiveness to erythropoietin with normal haemoglobin. Serum erythropoietin levels 2,994 Icelandic ancestry individuals, 1,193 non-array typed, familial imputed Icelandic ancestry individuals 68 Icelandic ancestry individuals Illumina [32554515] (imputed) 1 erythropoetin measurement http://www.ebi.ac.uk/efo/EFO_0008391 GCST006536 Genome-wide genotyping array 2018-10-05 30099483 Hwangbo Y 2018-08-06 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/30099483 Genome-wide Association Study Reveals Distinct Genetic Susceptibility of Thyroid Nodules from Thyroid Cancer. Thyroid nodules 811 Korean ancestry cases, 691 Korean ancestry controls 1,981 Korean ancestry cases, 3,100 Korean ancestry controls Affymetrix [3996558] (imputed) 2 thyroid nodule http://www.ebi.ac.uk/efo/EFO_1001436 GCST006387 Genome-wide genotyping array 2018-10-18 30103242 Karhausen JA 2018-08-13 Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/30103242 Genome-Wide Association Study Links Receptor Tyrosine Kinase Inhibitor Sprouty 2 to Thrombocytopenia after Coronary Artery Bypass Surgery. Thrombocytopenia in coronary artery bypass surgery 176 European ancestry cases, 268 European ancestry cases 76 European ancestry cases, 70 European ancestry cases Illumina [525066] 1 Thrombocytopenia http://purl.obolibrary.org/obo/HP_0001873 GCST006435 Genome-wide genotyping array 2018-11-29 30134952 Traglia M 2018-08-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/30134952 Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. Midgestational cytokine/chemokine levels (maternal genetic effect) 790 Hispanic, European, Asian, South Asian or African American individuals NA Affymetrix [629686] 3 gestational serum measurement, protein measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0007964, http://www.ebi.ac.uk/efo/EFO_0004747, http://www.ebi.ac.uk/efo/EFO_0005939 GCST006621 Genome-wide genotyping array 2018-11-29 30134952 Traglia M 2018-08-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/30134952 Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. Neonatal cytokine/chemokine levels (maternal genetic effect) 790 Hispanic, European, Asian, South Asian or African American individuals NA Affymetrix [629686] 3 protein measurement, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0004747, http://www.ebi.ac.uk/efo/EFO_0005939 GCST006625 Genome-wide genotyping array 2018-11-29 30134952 Traglia M 2018-08-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/30134952 Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. Midgestational cytokine/chemokine levels (fetal genetic effect) 764 Hispanic, European, Asian, South Asian or African American individuals NA Affymetrix [622716] 1 gestational serum measurement, fetal genotype effect measurement, protein measurement http://www.ebi.ac.uk/efo/EFO_0007964, http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0004747 GCST006623 Genome-wide genotyping array 2018-11-29 30134952 Traglia M 2018-08-22 Genome Med www.ncbi.nlm.nih.gov/pubmed/30134952 Cross-genetic determination of maternal and neonatal immune mediators during pregnancy. Neonatal cytokine/chemokine levels (fetal genetic effect) 764 Hispanic, European, Asian, South Asian or African American individuals NA Affymetrix [622716] 23 fetal genotype effect measurement, protein measurement http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0004747 GCST006622 Genome-wide genotyping array 2018-10-19 30113228 Torgerson DG 2018-08-16 Am J Physiol Lung Cell Mol Physiol www.ncbi.nlm.nih.gov/pubmed/30113228 Ancestry and Genetic Associations with Bronchopulmonary Dysplasia in Preterm Infants. Bronchopulmonary dysplasia in preterm infants 136 European ancestry cases, 82 African American cases, 28 Hispanic cases, 41 European ancestry controls, 51 African American controls, 14 Hispanic controls NA Affymetrix [8800000] (imputed) 12 bronchopulmonary dysplasia http://purl.obolibrary.org/obo/MONDO_0019091 GCST006460 Genome-wide genotyping array 2019-01-07 30102679 Hara M 2018-08-10 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/30102679 Genome-wide Association Study of Leisure-Time Exercise Behavior in Japanese Adults. Leisure-time exercise behaviour 1,789 Japanese ancestry physically active cases, 12,191 Japanese ancestry physically inactive controls 250 Japanese ancestry physically active cases, 1,786 Japanese ancestry physically inactive controls Illumina [up to 7094228] (imputed) 2 exercise http://www.ebi.ac.uk/efo/EFO_0000483 GCST006857 Genome-wide genotyping array 2019-01-07 30102679 Hara M 2018-08-10 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/30102679 Genome-wide Association Study of Leisure-Time Exercise Behavior in Japanese Adults. Leisure-time exercise behaviour (age-stratified) 6,749 Japanese ancestry active and inactive individuals aged over 56, 7,231 Japanese ancestry active and inactive individuals aged under 56 1,129 Japanese ancestry active and inactive individuals aged over 56, 907 Japanese ancestry active and inactive individuals aged under 56 Illumina [up to 7094228] (imputed) 3 exercise http://www.ebi.ac.uk/efo/EFO_0000483 GCST006858 Genome-wide genotyping array 2018-10-09 30108209 Ganjgahi H 2018-08-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30108209 Fast and powerful genome wide association of dense genetic data with high dimensional imaging phenotypes. Brain imaging measurements 175 European ancestry schizophrenia cases, 155 European ancestry controls NA NR [1376877] 0 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST006389 Genome-wide genotyping array 2018-11-05 30120429 Schlauch KA 2018-08-17 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/30120429 Single-nucleotide polymorphisms in a cohort of significantly obese women without cardiometabolic diseases. Obesity without metabolic disease 38 European ancestry cases, 32 European ancestry non-obese controls NA Affymetrix [710007] 14 metabolically healthy obesity http://www.ebi.ac.uk/efo/EFO_0009382 GCST006492 Genome-wide genotyping array 2018-12-11 30281874 Tanikawa C 2018-10-03 Cancer Sci www.ncbi.nlm.nih.gov/pubmed/30281874 A GWAS identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21. Gastric cancer 6,171 Japanese ancestry cases, 27,178 Japanese ancestry controls 5,336 Japanese ancestry cases, 11,726 Japanese ancestry controls Illumina [6573681] (imputed) 6 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST006707 Genome-wide genotyping array 2018-12-11 30281099 Fadista J 2018-10-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/30281099 Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis. Infantile hypertrophic pyloric stenosis 1,395 Danish ancestry cases, 4,438 Danish ancestry controls 1,794 European ancestry cases, 633 Hispanic ancestry cases, 1,875 European ancestry controls, 633 Hispanic ancestry controls Illumina [6576307] (imputed) 13 infantile hypertrophic pyloric stenosis http://www.ebi.ac.uk/efo/EFO_0004707 GCST006705 Genome-wide genotyping array 2018-09-28 30108127 Hoffmann TJ 2018-08-14 Genetics www.ncbi.nlm.nih.gov/pubmed/30108127 A Large Multi-ethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. Body mass index 315,347 European ancestry individuals, 8,322 Hispanic/Latino individuals, 7,290 East Asian ancestry individuals, 3,069 African American individuals, 459 South Asian ancestry individuals 431,743 European ancestry individuals, 9,275 South Asian ancestry individuals, 8,261 African British individuals, 1,822 East Asian ancestry individuals, 7,620 individuals Affymetrix [at least 28613428] (imputed) 289 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST006368 Genome-wide genotyping array 2018-11-29 30287806 Zhou H 2018-10-04 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30287806 Genome-wide association study identifies glutamate ionotropic receptor GRIA4 as a risk gene for comorbid nicotine dependence and major depression. Nicotine dependence and major depression (severity of comorbidity) 3,724 African American individuals NA Illumina [9520174] (imputed) 52 nicotine dependence symptom count, depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0009262, http://www.ebi.ac.uk/efo/EFO_0007006 GCST006631 Genome-wide genotyping array 2018-07-10 29632299 Vijayakrishnan J 2018-04-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/29632299 Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. Acute lymphoblastic leukemia in childhood (B cell precursor) 2,442 European ancestry cases, 14,609 European ancestry controls NA Illumina [6755715] (imputed) 11 B-cell acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000094 GCST005832 Genome-wide genotyping array 2018-10-09 30102696 Chen Y 2018-08-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30102696 A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. Biliary atresia 343 European ancestry cases, 1,716 European ancestry controls 156 European ancestry cases, 212 European ancestry controls Illumina [1171073] (imputed) 3 biliary atresia http://purl.obolibrary.org/obo/MONDO_0008867 GCST006390 Genome-wide genotyping array 2018-10-17 30150663 Pasman JA 2018-08-27 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/30150663 GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia. Cannabis use 184,765 European ancestry individuals NA Affymetrix, Illumina [11733371] (imputed) 8 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST006421 Genome-wide genotyping array 2019-01-21 30104601 Ren H 2018-08-13 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30104601 Genes associated with anhedonia: a new analysis in a large clinical trial (GENDEP). Anhedonia in major depressive disorder 759 European ancestry individuals 1,351 individuals Illumina [1313315] (imputed) 0 anhedonia measurement http://www.ebi.ac.uk/efo/EFO_0009587 GCST006927 Genome-wide genotyping array 2019-10-28 30971809 Wendt FR 2019-04-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30971809 A genome-wide association study of tramadol metabolism from post-mortem samples. Tramadol metabolism (O-desmethyltramadol to tramadol ratio) 37 Finnish ancestry deceased individuals 99 Finnish ancestry individuals Illumina [1499150] 0 response to opioid http://www.ebi.ac.uk/efo/EFO_0008541 GCST008967 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Total hippocampal volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 8 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST006871 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Presubiculum volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST006872 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Subiculum volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST006873 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal subfield CA1 volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 2 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST006874 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal subfield CA3 volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST006875 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal subfield CA4 volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST006876 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Dentate gyrus granule cell layer volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 granule cell layer dentate gyrus volume http://www.ebi.ac.uk/efo/EFO_0009403 GCST006877 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Dentate gyrus molecular layer volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST006878 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal fissure volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 hippocampal fissure volume http://www.ebi.ac.uk/efo/EFO_0009404 GCST006880 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal tail volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 7 hippocampal tail volume http://www.ebi.ac.uk/efo/EFO_0009398 GCST006881 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Fimbria volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST006882 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. HATA volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST006883 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Parasubiculum volume (corrected for total hippocampal volume) 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 parasubiculum volume http://www.ebi.ac.uk/efo/EFO_0009405 GCST006884 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Presubiculum volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST006885 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Subiculum volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 4 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST006886 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal subfield CA1 volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 3 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST006887 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal subfield CA3 volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 3 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST006888 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal subfield CA4 volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 5 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST006889 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Dentate gyrus granule cell layer volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 5 granule cell layer dentate gyrus volume http://www.ebi.ac.uk/efo/EFO_0009403 GCST006890 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Dentate gyrus molecular layer volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 5 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST006891 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal fissure volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 hippocampal fissure volume http://www.ebi.ac.uk/efo/EFO_0009404 GCST006892 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Hippocampal tail volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 7 hippocampal tail volume http://www.ebi.ac.uk/efo/EFO_0009398 GCST006870 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Fimbria volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST006893 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. HATA volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST006894 Genome-wide genotyping array 2019-01-11 30279459 van der Meer D 2018-10-02 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30279459 Brain scans from 21,297 individuals reveal the genetic architecture of hippocampal subfield volumes. Parasubiculum volume 21,297 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 parasubiculum volume http://www.ebi.ac.uk/efo/EFO_0009405 GCST006895 Genome-wide genotyping array 2019-03-20 30270018 Zhang Q 2018-09-09 J Diabetes Complications www.ncbi.nlm.nih.gov/pubmed/30270018 Additional common variants associated with type 2 diabetes and coronary artery disease detected using a pleiotropic cFDR method. Type 2 diabetes or coronary artery disease (pleiotropy) 12,171 European ancestry type 2 diabetes cases, 22,233 European ancestry coronary artery disease cases, 121,624 European ancestry controls NA NR [NR] 0 type 2 diabetes mellitus, coronary artery disease http://purl.obolibrary.org/obo/MONDO_0005148, http://www.ebi.ac.uk/efo/EFO_0001645 GCST007359 Genome-wide genotyping array 2018-11-30 30276832 Edwards AC 2018-10-01 Alcohol Clin Exp Res www.ncbi.nlm.nih.gov/pubmed/30276832 Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. Initial alcohol sensitivity 6,039 European ancestry individuals, 892 African ancestry individuals, 408 American ancestry individuals NA Affymetrix, Illumina [15642250] (imputed) 34 response to alcohol http://www.ebi.ac.uk/efo/EFO_0005526 GCST006633 Genome-wide genotyping array 2019-02-13 30284222 Brcic L 2018-10-03 J Endocrinol Invest www.ncbi.nlm.nih.gov/pubmed/30284222 Genome-wide association analysis suggests novel loci for Hashimoto's thyroiditis. Hashimoto thyroiditis 405 Croatian ancestry cases, 433 Croatian ancestry controls 303 Croatian ancestry cases, 302 Croatian ancestry controls Illumina [8621046] (imputed) 1 Hashimoto's thyroiditis http://www.ebi.ac.uk/efo/EFO_0003779 GCST007138 Genome-wide genotyping array 2019-03-20 30206298 Spear ML 2018-09-12 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/30206298 A genome-wide association and admixture mapping study of bronchodilator drug response in African Americans with asthma. Bronchodilator response in asthma 949 African American cases, 1,830 Latino cases 1,615 African American cases, 416 Latino cases Affymetrix [up to 9605653] (imputed) 0 response to bronchodilator http://purl.obolibrary.org/obo/GO_0097366 GCST007360 Genome-wide genotyping array 2019-08-23 30289108 Li W 2018-07-07 Eur Urol www.ncbi.nlm.nih.gov/pubmed/30289108 Genome-wide Scan Identifies Role for AOX1 in Prostate Cancer Survival. Prostate cancer mortality 245 European ancestry lethal cases, 808 European ancestry long-term survivor cases 172 European ancestry lethal cases, 1380 European ancestry long-term survivor cases Illumina [6126633] (imputed) 0 survival time, prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0000714, http://www.ebi.ac.uk/efo/EFO_0001663 GCST008493 Genome-wide genotyping array 2019-04-09 30206230 Offenbacher S 2018-09-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30206230 GWAS for Interleukin-1β levels in gingival crevicular fluid identifies IL37 variants in periodontal inflammation. High IL-1beta levels in gingival crevicular fluid 4,910 European American individuals NA Affymetrix [656292] (imputed) 178 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST007542 Genome-wide genotyping array 2018-09-19 30054556 Akiyama M 2018-07-27 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30054556 Genome-wide association study suggests four variants influencing outcomes with ranibizumab therapy in exudative age-related macular degeneration. Response to ranibizumab in age-related macular degeneration (exudative) 361 Japanese ancestry responder cases, 73 Japanese ancestry non-responder controls 363 Japanese ancestry responder cases, 122 Japanese ancestry non-responder controls Illumina [6826359] (imputed) 4 response to ranibizumab http://www.ebi.ac.uk/efo/EFO_0008348 GCST006277 Genome-wide genotyping array 2018-10-22 30093639 Machiela MJ 2018-08-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30093639 Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility. Ewing sarcoma 733 European ancestry cases, 1,346 European ancestry controls 657 European ancestry cases, 4,078 European ancestry controls Illumina [6876682] (imputed) 4 Ewing sarcoma http://www.ebi.ac.uk/efo/EFO_0000174 GCST006467 Genome-wide genotyping array 2018-11-28 30287856 Zheng R 2018-10-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30287856 Genome-wide association study identifies two risk loci for tuberculosis in Han Chinese. Tuberculosis 833 Han Chinese ancestry cases, 1,220 Han Chinese ancestry controls 2,116 Han Chinese ancestry cases, 3,870 Han Chinese ancestry controls Affymetrix [5374021] (imputed) 2 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST006619 Genome-wide genotyping array 2019-04-12 30696823 Jones SE 2019-01-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30696823 Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms. Morning person 252,287 European ancestry cases, 150,908 European ancestry controls 120,478 European ancestry cases, 127,622 European ancestry controls Affymetrix [11880941] (imputed) 213 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST007565 Genome-wide genotyping array 2019-04-15 30696823 Jones SE 2019-01-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30696823 Genome-wide association analyses of chronotype in 697,828 individuals provides insights into circadian rhythms. Chronotype 449,734 European ancestry individuals 248,098 European ancestry individuals Affymetrix [11880941] (imputed) 440 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST007576 Genome-wide genotyping array 2019-03-19 30649180 Luo Q 2019-01-16 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/30649180 Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study. Voxel-wise structural brain imaging measurements 1,721 European ancestry adolescent individuals 6,932 British ancestry individuals Illumina [466114] 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST007357 Genome-wide genotyping array 2019-02-01 30655502 Levey DF 2019-01-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30655502 Genetic associations with suicide attempt severity and genetic overlap with major depression. Suicide attempt severity 2,439 European ancestry individuals, 3,881 African American individuals 9,382 European ancestry individuals, 1,488 African American individuals, 2,963 Latino individuals Illumina [at least 550601] (imputed) 2 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST007019 Genome-wide genotyping array 2019-08-23 30088374 Park HW 2018-09-01 Allergy Asthma Immunol Res www.ncbi.nlm.nih.gov/pubmed/30088374 The Fas Signaling Pathway Is a Common Genetic Risk Factor for Severe Cutaneous Drug Adverse Reactions Across Diverse Drugs. Severe cutaneous adverse drug reactions 68 Korean ancestry cases, 272 Korean ancestry controls 38 Korean ancestry cases, 152 Korean ancestry controls Affymetrix [NR] 0 severe cutaneous adverse reaction http://www.ebi.ac.uk/efo/EFO_0006346 GCST008492 Genome-wide genotyping array 2019-08-07 30104761 Zhou W 2018-08-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30104761 Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. Thyroid cancer 358 European ancestry cases, 407,399 European ancestry controls NA Affymetrix [28000000] (imputed) 1 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST008371 Genome-wide genotyping array 2019-08-07 30104761 Zhou W 2018-08-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30104761 Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. Coronary artery disease 31,355 European ancestry cases, 377,103 European ancestry controls NA Affymetrix [28000000] (imputed) 40 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST008370 Genome-wide genotyping array 2019-08-07 30104761 Zhou W 2018-08-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30104761 Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. Glaucoma 4,462 European ancestry cases, 397,761 European ancestry controls NA Affymetrix [28000000] (imputed) 11 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST008373 Genome-wide genotyping array 2019-08-07 30104761 Zhou W 2018-08-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30104761 Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. Colorectal cancer 4,562 European ancestry cases, 382,756 European ancestry controls NA Affymetrix [28000000] (imputed) 3 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST008372 Genome-wide genotyping array 2018-10-16 30134085 Zhang H 2018-07-01 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/30134085 Genome-wide association study of cognitive flexibility assessed by the Wisconsin Card Sorting Test. Cognitive flexibility 2,589 African American individuals, 2,284 European ancestry individuals NA Illumina [9722417] (imputed) 5 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST006406 Genome-wide genotyping array 2019-01-11 30054458 Xue A 2018-07-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30054458 Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Type 2 diabetes 61,714 European ancestry cases, 1,178 Pakistani ancestry cases, 593,952 European ancestry controls, 2,472 Pakistani ancestry controls NA NR [5035015] (imputed) 139 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST006867 Genome-wide genotyping array 2019-01-11 30054458 Xue A 2018-07-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30054458 Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes. Type 2 diabetes 21,147 European ancestry cases, 434,460 European ancestry controls NA NR [10849711] (imputed) 11 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST006868 Genome-wide genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (recessive genetic model) 288,492 European ancestry individuals, up to 15,687 African American individuals, up to 29,315 South Asian ancestry individuals, up to 6,800 East Asian ancestry individuals, up to 4,075 Hispanic ancestry individuals 132,177 European ancestry individuals Affymetrix, Illumina [at least 228985] 1 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007484 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (additive genetic model) 288,492 European ancestry individuals 132,177 European ancestry individuals Affymetrix, Illumina [at least 228985] 56 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007487 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (additive genetic model) 288,492 European ancestry individuals, up to 15,687 African American individuals, up to 29,315 South Asian ancestry individuals, up to 6,800 East Asian ancestry individuals, up to 4,075 Hispanic ancestry individuals 132,177 European ancestry individuals Affymetrix, Illumina [at least 228985] 57 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007483 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (recessive genetic model) 288,492 European ancestry individuals 132,177 European ancestry individuals Affymetrix, Illumina [at least 228985] 2 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007491 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (additive genetic model) up to 130,976 European ancestry men, up to 164,238 African American, South Asian, East Asian and Hispanic ancestry men up to 62,500 European ancestry men Affymetrix, Illumina [at least 228985] 18 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007492 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (recessive genetic model) up to 130,976 European ancestry men, up to 164,238 African American, South Asian, East Asian and Hispanic ancestry men up to 62,500 European ancestry men Affymetrix, Illumina [at least 228985] 1 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007493 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (additive genetic model) up to 130,976 European ancestry men up to 62,500 European ancestry men Affymetrix, Illumina [at least 228985] 17 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007494 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (recessive genetic model) up to 130,976 European ancestry men up to 62,500 European ancestry men Affymetrix, Illumina [at least 228985] 1 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007496 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (additive genetic model) up to 157,516 European ancestry women, up to 180,131 African American, South Asian, East Asian and Hispanic ancestry women up to 62,368 European ancestry women Affymetrix, Illumina [at least 228985] 47 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007500 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (recessive genetic model) up to 157,516 European ancestry women, up to 180,131 African American, South Asian, East Asian and Hispanic ancestry women up to 62,368 European ancestry women Affymetrix, Illumina [~ 228985] 2 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007501 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (additive genetic model) up to 157,516 European ancestry women up to 62,368 European ancestry women Affymetrix, Illumina [at least 228985] 43 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007502 Genome-wide genotyping array, Exome genotyping array 2019-04-03 30778226 Justice AE 2019-02-18 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30778226 Protein-coding variants implicate novel genes related to lipid homeostasis contributing to body-fat distribution. Waist-to-hip ratio adjusted for BMI (recessive genetic model) up to 157,516 European ancestry women up to 62,368 European ancestry women Affymetrix, Illumina [at least 228985] 2 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST007503 Genome-wide genotyping array, Exome genotyping array 2018-11-26 30275531 Klarin D 2018-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30275531 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. HDL cholesterol 215,551 European ancestry individuals, 57,332 African American individuals, 24,743 Hispanic individuals Up to 319,677 individuals Affymetrix [up to 31400000] (imputed) 158 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST006611 Genome-wide genotyping array 2018-11-26 30275531 Klarin D 2018-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30275531 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. LDL cholesterol 215,551 European ancestry individuals, 57,332 African American individuals, 24,743 Hispanic individuals Up to 319,677 individuals Affymetrix [up to 31400000] (imputed) 125 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST006612 Genome-wide genotyping array 2018-11-26 30275531 Klarin D 2018-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30275531 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. Triglycerides 215,551 European ancestry individuals, 57,332 African American individuals, 24,743 Hispanic individuals Up to 319,677 individuals Affymetrix [up to 31400000] (imputed) 151 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST006613 Genome-wide genotyping array 2018-11-26 30275531 Klarin D 2018-10-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30275531 Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. Total cholesterol levels 215,551 European ancestry individuals, 57,332 African American individuals, 24,743 Hispanic individuals Up to 319,677 individuals Affymetrix [up to 31400000] (imputed) 140 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST006614 Genome-wide genotyping array 2019-02-21 30285260 Ikeda M 2018-10-03 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/30285260 Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. Schizophrenia 1,940 Japanese ancestry cases, 7,408 Japanese ancestry controls 4,071 Japanese ancestry cases, 54,470 Japanese ancestry controls Illumina [6627481] (imputed) 13 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST007205 Genome-wide genotyping array 2019-02-21 30285260 Ikeda M 2018-10-03 Schizophr Bull www.ncbi.nlm.nih.gov/pubmed/30285260 Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. Schizophrenia 14,023 East Asian ancestry cases, 33,640 European ancestry cases, 31,505 East Asian ancestry controls, 43,456 European ancestry controls NA Illumina [6627481] (imputed) 472 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST007201 Genome-wide genotyping array 2018-09-20 30068317 Li X 2018-08-01 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/30068317 Genome-wide association study of lung function and clinical implication in heavy smokers. Post bronchodilator percent predicted FEV1 in smoking 1,086 European ancestry COPD cases, 559 European ancestry controls NA Illumina [635970] 8 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST006309 Genome-wide genotyping array 2018-09-20 30068317 Li X 2018-08-01 BMC Med Genet www.ncbi.nlm.nih.gov/pubmed/30068317 Genome-wide association study of lung function and clinical implication in heavy smokers. Post bronchodilator FEV1/FVC ratio in smoking 1,086 European ancestry COPD cases, 559 European ancestry controls NA Illumina [635970] 8 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST006310 Genome-wide genotyping array 2018-11-13 30087453 Yilmaz Z 2018-08-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30087453 Examination of the shared genetic basis of anorexia nervosa and obsessive-compulsive disorder. Anorexia nervosa or obsessive-compulsive disorder 3,495 European ancestry anorexia nervosa cases, 2,688 European ancestry obsessive-compulsive disorder cases, 18,013 European ancestry controls NA NR [7461827] (imputed) 3 obsessive-compulsive disorder, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0004242, http://purl.obolibrary.org/obo/MONDO_0005351 GCST006576 Genome-wide genotyping array 2018-10-16 30067744 Howe LJ 2018-08-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30067744 Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology. Philtrum width 6,136 European ancestry individuals NA Illumina [at least 968515] (imputed) 2 lip morphology measurement http://www.ebi.ac.uk/efo/EFO_0007845 GCST006407 Genome-wide genotyping array 2018-10-17 30067744 Howe LJ 2018-08-01 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30067744 Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphology. Nonsyndromic cleft lip with or without cleft palate 638 European ancestry trios, 178 European ancestry duos, 399 cases, 1,318 controls NA Illumina [NR] 6 Cleft palate, cleft lip http://purl.obolibrary.org/obo/HP_0000175, http://www.ebi.ac.uk/efo/EFO_0003959 GCST006415 Genome-wide genotyping array 2018-10-15 30169657 Ashar FN 2018-08-28 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/30169657 A comprehensive evaluation of the genetic architecture of sudden cardiac arrest. Sudden cardiac arrest up to 3,939 European ancestry cases, up to 25,989 European ancestry controls up to 4,751 European ancestry cases, up to 35,582 European ancestry controls, 152 African American cases, 176 African American controls, 225 Asian American cases, 199 Asian American controls Affymetrix, Illumina [at least 306655] (imputed) 2 sudden cardiac arrest http://www.ebi.ac.uk/efo/EFO_0004278 GCST006401 Genome-wide genotyping array 2018-11-27 30161160 Onishi H 2018-08-30 PLoS One www.ncbi.nlm.nih.gov/pubmed/30161160 A genome-wide association study identifies three novel genetic markers for response to tamoxifen: A prospective multicenter study. Response to tamoxifen in oestrogen receptor positive/HER2 negative breast cancer 275 East Asian ancestry individuals 72 East Asian or Asian ancestry individuals Illumina [519335] (imputed) 2 response to tamoxifen http://www.ebi.ac.uk/efo/EFO_0009391 GCST006615 Genome-wide genotyping array 2018-10-17 30158200 Trajanoska K 2018-08-29 BMJ www.ncbi.nlm.nih.gov/pubmed/30158200 Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study. Fractures 37,857 European or East Asian cases, 227,116 European or East Asian controls 147,200 European ancestry cases, 150,085 European ancestry controls Affymetrix, Illumina [2539801] (imputed) 17 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST006423 Genome-wide genotyping array 2018-10-17 30158200 Trajanoska K 2018-08-29 BMJ www.ncbi.nlm.nih.gov/pubmed/30158200 Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study. Fractures 37,857 European or East Asian ancestry cases, 227,116 European or East Asian ancestry controls 18,779 European, East Asian or other ancestry cases, 32,078 European, East Asian or other ancestry controls Affymetrix, Illumina [2539801] (imputed) 5 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST006422 Genome-wide genotyping array 2018-10-18 30048462 Kim SK 2018-07-26 PLoS One www.ncbi.nlm.nih.gov/pubmed/30048462 Identification of 613 new loci associated with heel bone mineral density and a polygenic risk score for bone mineral density, osteoporosis and fracture. Heel bone mineral density 394,929 European ancestry individuals NA Affymetrix [20259828] (imputed) 1587 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST006433 Genome-wide genotyping array 2018-11-29 30224653 Evangelou E 2018-09-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30224653 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Systolic blood pressure 757,601 European ancestry individuals 249,262 European ancestry individuals Affymetrix, Illumina [~ 7100000] (imputed) 130 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST006624 Genome-wide genotyping array 2018-11-29 30224653 Evangelou E 2018-09-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30224653 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Diastolic blood pressure 757,601 European ancestry individuals 249,262 European ancestry individuals Affymetrix, Illumina [~ 7100000] (imputed) 91 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST006630 Genome-wide genotyping array 2018-11-29 30224653 Evangelou E 2018-09-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30224653 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Pulse pressure 757,601 European ancestry individuals 249,262 European ancestry individuals Affymetrix, Illumina [~ 7100000] (imputed) 104 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST006629 Genome-wide genotyping array 2018-11-29 30224653 Evangelou E 2018-09-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30224653 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Systolic blood pressure 757,601 European ancestry individuals NA Affymetrix, Illumina [~ 7100000] (imputed) 60 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST006628 Genome-wide genotyping array 2018-11-29 30224653 Evangelou E 2018-09-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30224653 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Diastolic blood pressure 757,601 European ancestry individuals NA Affymetrix, Illumina [~ 7100000] (imputed) 103 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST006627 Genome-wide genotyping array 2018-11-29 30224653 Evangelou E 2018-09-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/30224653 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. Pulse pressure 757,601 European ancestry individuals NA Affymetrix, Illumina [~ 7100000] (imputed) 47 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST006626 Genome-wide genotyping array 2018-10-17 30219690 Heinzman JT 2018-09-07 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/30219690 GWAS and systems biology analysis of depressive symptoms among smokers from the COPDGene cohort. Depression in smokers 1,622 European ancestry cases, 391 African American cases, 4,954 European ancestry controls, 2,749 African American controls NA Illumina [NR] (imputed) 54 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST006427 Genome-wide genotyping array 2019-04-18 30219835 Lin WY 2018-09-13 Brief Bioinform www.ncbi.nlm.nih.gov/pubmed/30219835 Polygenic approaches to detect gene-environment interactions when external information is unavailable. Blood pressure x alcohol consumption interaction 1,764 East Asian ancestry alcohol-drinking individuals, 14,779 East Asian ancestry non-alcohol-drinking individuals NA NR [601531] 0 blood pressure, alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0004325, http://www.ebi.ac.uk/efo/EFO_0007878 GCST007617 Genome-wide genotyping array 2019-04-18 30219835 Lin WY 2018-09-13 Brief Bioinform www.ncbi.nlm.nih.gov/pubmed/30219835 Polygenic approaches to detect gene-environment interactions when external information is unavailable. Blood pressure (smoking interaction) 4,104 East Asian ancestry smoking individuals, 12,429 East Asian ancestry non-smoking individuals NA NR [601531] 0 smoking status measurement, blood pressure http://www.ebi.ac.uk/efo/EFO_0006527, http://www.ebi.ac.uk/efo/EFO_0004325 GCST007618 Genome-wide genotyping array 2019-05-22 30946743 Li Z 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946743 Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis. Ankylosing spondylitis 921 Turkish ancestry cases, 907 Turkish ancestry controls, 422 Iranian ancestry cases, 754 Iranian ancestry controls NA Illumina [up to 294091] 23 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST007844 Genome-wide genotyping array 2019-04-09 30226466 Valimaki N 2018-09-18 Elife www.ncbi.nlm.nih.gov/pubmed/30226466 Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability. Uterine fibroids 15,910 European ancestry cases, 408,571 European ancestry controls 1,504 European ancestry cases, 296 Black African ancestry cases, 668 Afro-Caribbean ancestry cases, 203 Indian ancestry cases, 20,133 European ancestry controls, 1,256 Black African ancestry controls, 2,041 Afro-Caribbean ancestry controls, 2,567 Indian ancestry controls Affymetrix [8300000] (imputed) 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST007548 Genome-wide genotyping array 2019-04-30 30922102 Pardinas AF 2019-03-29 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30922102 Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism. Plasma norclozapine levels in treatment-resistant schizophrenia 2,989 European ancestry individuals NA Illumina [~ 7500000] (imputed) 2 plasma N-desmethylclozapine measurement http://www.ebi.ac.uk/efo/EFO_0600039 GCST007686 Genome-wide genotyping array 2019-04-30 30922102 Pardinas AF 2019-03-29 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30922102 Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism. Plasma clozapine-norclozapine ratio in treatment-resistant schizophrenia 2,989 European ancestry individuals NA Illumina [~ 7500000] (imputed) 3 plasma clozapine-to-N-desmethylclozapine ratio measurement http://www.ebi.ac.uk/efo/EFO_0600040 GCST007684 Genome-wide genotyping array 2019-04-30 30922102 Pardinas AF 2019-03-29 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/30922102 Pharmacogenomic Variants and Drug Interactions Identified Through the Genetic Analysis of Clozapine Metabolism. Plasma clozapine levels in treatment-resistant schizophrenia 2,989 European ancestry individuals NA Illumina [~ 7500000] (imputed) 1 plasma clozapine measurement http://www.ebi.ac.uk/efo/EFO_0600038 GCST007685 Genome-wide genotyping array 2019-03-15 30659137 Traylor M 2019-01-18 Neurology www.ncbi.nlm.nih.gov/pubmed/30659137 Genetic variation in PLEKHG1 is associated with white matter hyperintensities (n = 11,226). White matter hyperintensity volume 8,429 European ancestry individuals, 2,797 European ancestry individuals with ischemic stroke 1,202 European ancestry individuals Affymetrix, Illumina [at least 39131578] (imputed) 3 white matter hyperintensity measurement http://www.ebi.ac.uk/efo/EFO_0005665 GCST007305 Genome-wide genotyping array 2018-11-05 29691896 Keaton JM 2018-04-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29691896 Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans. Type 2 diabetes (SNP x SNP interaction, 2df) 2,452 African American cases, 3,772 African American controls NA Affymetrix [9085034] (imputed) 22 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST006495 Genome-wide genotyping array 2018-11-05 29691896 Keaton JM 2018-04-24 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/29691896 Genome-wide interaction with the insulin secretion locus MTNR1B reveals CMIP as a novel type 2 diabetes susceptibility gene in African Americans. Type 2 diabetes (SNP x SNP interaction, 1df) 2,452 African American cases, 3,772 African American controls NA Affymetrix [9085034] (imputed) 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST006494 Genome-wide genotyping array 2019-05-16 30926877 Brcic L 2019-03-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30926877 Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis. Anti-thyroid peroxidase (TPOAb) levels in Hashimoto's thyroiditis 405 European ancestry cases NA Illumina [6007542] (imputed) 11 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST007830 Genome-wide genotyping array 2019-05-16 30926877 Brcic L 2019-03-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30926877 Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis. Anti-thyroglobulin (TgAb) levels in Hashimoto's thyroiditis 405 European ancestry cases NA Illumina [6007542] (imputed) 9 anti-thyroglobulin antibody measurement http://www.ebi.ac.uk/efo/EFO_0009896 GCST007831 Genome-wide genotyping array 2019-05-23 30926877 Brcic L 2019-03-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30926877 Genome-wide association analysis suggests novel loci underlying thyroid antibodies in Hashimoto's thyroiditis. Anti-thyroid peroxidase (TPOAb) and anti-thyroglobulin (TgAb) levels in Hashimoto's thyroiditis 405 European ancestry cases NA Illumina [6007542] (imputed) 10 thyroid peroxidase antibody measurement, anti-thyroglobulin antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666, http://www.ebi.ac.uk/efo/EFO_0009896 GCST007851 Genome-wide genotyping array 2018-11-07 22997280 Ho JE 2012-09-20 Clin Chem www.ncbi.nlm.nih.gov/pubmed/22997280 Clinical and genetic correlates of growth differentiation factor 15 in the community. Growth differentiation factor-15 levels 3,889 European ancestry individuals NA Affymetrix [NR] (imputed) 2 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST006519 Genome-wide genotyping array 2019-10-23 30920090 Trochet H 2019-03-28 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30920090 Bayesian meta-analysis across genome-wide association studies of diverse phenotypes. Multiple traits (pleiotropy) 1,787 European ancestry ankylosing spondylitis cases, 9,772 European ancestry multiple sclerosis cases, 2,178 European ancestry psoriasis cases, 2,361 European ancestry ulcerative colitis cases, 844 European ancestry large vessel ischemic stroke cases, 580 European ancestry small vessel ischemic stroke cases, 790 European ancestry cardioembolic ischemic stroke cases, 2,794 European ancestry individuals with reading score and mathematics score measurements, 1,606 European ancestry schizophrenia cases, 1,239 European ancestry psychosis cases, 1,705 European ancestry Parkinson's disease cases, 1,852 European ancestry Barrett's esophagus cases, 1,024 European ancestry individuals with metformin response measurements, 2,302 European ancestry glaucoma cases, 429 Kenyan ancestry pneumococcal bacteremia cases, 1,107 Kenyan ancestry other bacteremia cases, 357 Brazilian ancestry visceral leishmaniasis cases, 989 Indian ancestry visceral leishmaniasis cases, 23,008 European ancestry controls, 2,677 Kenyan ancestry controls, 1,613 Brazilian ancestry controls, 1,089 Indian ancestry controls NA Affymetrix, Illumina [2058911] (imputed) 0 Barrett's esophagus, cardioembolic stroke, ankylosing spondylitis, psoriasis, pneumococcal bacteremia, mathematical ability, Parkinson disease, multiple sclerosis, bacteriemia, small vessel stroke, reading, schizophrenia, psychosis, large artery stroke, visceral Leishmaniasis, ulcerative colitis, glaucoma, response to metformin http://www.ebi.ac.uk/efo/EFO_0000280, http://www.ebi.ac.uk/efo/EFO_1001976, http://www.ebi.ac.uk/efo/EFO_0003898, http://www.ebi.ac.uk/efo/EFO_0000676, http://www.ebi.ac.uk/efo/EFO_1001925, http://www.ebi.ac.uk/efo/EFO_0004875, http://purl.obolibrary.org/obo/MONDO_0005180, http://purl.obolibrary.org/obo/MONDO_0005301, http://www.ebi.ac.uk/efo/EFO_0003033, http://www.ebi.ac.uk/efo/EFO_1001504, http://www.ebi.ac.uk/efo/EFO_0005229, http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0005407, http://www.ebi.ac.uk/efo/EFO_0005524, http://www.ebi.ac.uk/efo/EFO_0005045, http://www.ebi.ac.uk/efo/EFO_0000729, http://purl.obolibrary.org/obo/MONDO_0005041, http://purl.obolibrary.org/obo/GO_1901558 GCST008910 Genome-wide genotyping array 2019-07-08 30921485 Bejaoui Y 2019-03-28 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/30921485 Genome-wide association study of psoriasis in an Egyptian population. Psoriasis 215 Egyptian ancestry cases, 416 Egyptian ancestry controls 321 Egyptian ancestry cases, 253 Egyptian ancestry controls Illumina [312245] 6 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST008096 Genome-wide genotyping array 2019-04-17 30980028 de Kovel CGF 2019-04-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30980028 The molecular genetics of hand preference revisited. Handedness (Left-handed vs. non-left-handed) 31,856 British ancestry cases, 299,181 British ancestry controls NA Affymetrix [~ 15000000] (imputed) 3 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST007592 Genome-wide genotyping array 2019-04-17 30980028 de Kovel CGF 2019-04-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30980028 The molecular genetics of hand preference revisited. Handedness (Right-handed vs. non-right-handed) 293,857 British ancestry cases, 37,180 British ancestry controls NA Affymetrix [~ 15000000] (imputed) 3 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST007594 Genome-wide genotyping array 2019-04-17 30980028 de Kovel CGF 2019-04-12 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30980028 The molecular genetics of hand preference revisited. Ambidextrousness 5,324 British ancestry cases, 325,713 British ancestry controls NA Affymetrix [~ 15000000] (imputed) 0 handedness http://www.ebi.ac.uk/efo/EFO_0009902 GCST007593 Genome-wide genotyping array 2018-09-06 29703846 Wei WQ 2018-04-27 Circulation www.ncbi.nlm.nih.gov/pubmed/29703846 LPA Variants are Associated with Residual Cardiovascular Risk in Patients Receiving Statins. Coronary heart disease events during statin therapy 3,088 European ancestry cases, 11 cases, 7,587 European ancestry controls, 94 controls 139 European ancestry cases, 21 cases, 990 European ancestry controls, 122 controls Illumina [~ 10000000] (imputed) 0 response to statin, cardiovascular event measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0006919 GCST006217 Genome-wide genotyping array 2019-08-06 31050781 Zhao SX 2019-05-03 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/31050781 Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study. Thyrotoxic hypokalemic periodic paralysis in Graves disease 171 Han Chinese ancestry cases with TPP, 1,404 Han Chinese ancestry cases without TPP NA Illumina [2752055] (imputed) 5 thyrotoxic periodic paralysis http://purl.obolibrary.org/obo/MONDO_0019201 GCST008364 Genome-wide genotyping array 2019-08-06 31050781 Zhao SX 2019-05-03 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/31050781 Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study. Thyrotoxic hypokalemic periodic paralysis and Graves disease 171 Han Chinese ancestry cases, 2,160 Han Chinese ancestry controls 362 Han Chinese ancestry cases, 1,089 Han Chinese ancestry controls Illumina [2752055] (imputed) 18 Graves disease, thyrotoxic periodic paralysis http://www.ebi.ac.uk/efo/EFO_0004237, http://purl.obolibrary.org/obo/MONDO_0019201 GCST008365 Genome-wide genotyping array 2019-02-19 30242048 Chen B 2018-09-21 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30242048 Genomic analyses of visual cognition: perceptual rivalry and top-down control. Perceptual rivalry (Necker cube stimulus) 1,880 Han Chinese ancestry individuals 748 Han Chinese ancestry individuals Illumina [7990224] (imputed) 0 visual perception measurement http://www.ebi.ac.uk/efo/EFO_0009700 GCST007176 Genome-wide genotyping array 2019-02-19 30242048 Chen B 2018-09-21 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30242048 Genomic analyses of visual cognition: perceptual rivalry and top-down control. Perceptual rivalry (voluntary modulation strength) 1,876 Han Chinese ancestry individuals 744 Han Chinese ancestry individuals Illumina [7989184] (imputed) 1 visual perception measurement http://www.ebi.ac.uk/efo/EFO_0009700 GCST007178 Genome-wide genotyping array 2019-02-19 30242048 Chen B 2018-09-21 J Neurosci www.ncbi.nlm.nih.gov/pubmed/30242048 Genomic analyses of visual cognition: perceptual rivalry and top-down control. Perceptual rivalry (binocular rivalry task) 2,097 Han Chinese ancestry individuals 870 Han Chinese ancestry individuals Illumina [7992300] (imputed) 0 visual perception measurement http://www.ebi.ac.uk/efo/EFO_0009700 GCST007177 Genome-wide genotyping array 2018-08-13 29662168 Hysi PG 2018-04-16 Nat Genet www.ncbi.nlm.nih.gov/pubmed/29662168 Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability. Hair color 290,891 European ancestry individuals 27,865 European ancestry individuals Affymetrix, Illumina [at least 560000] (imputed) 24 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST006075 Genome-wide genotyping array 2018-09-25 29654602 Laville V 2018-04-13 Exp Dermatol www.ncbi.nlm.nih.gov/pubmed/29654602 A Genome-Wide Association Study identifies new genes potentially associated with eyelid sagging. Upper eyelid sagging severity 29 French ancestry individuals with grade 0-I sagging, 107 French ancestry individuals with grade II sagging, 192 French ancestry individuals with grade III sagging, 174 French ancestry individuals with grade IV-V sagging NA Illumina [795063] 4 eyelid sagging measurement http://www.ebi.ac.uk/efo/EFO_0009360 GCST006365 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty stopping worrying during worst period of anxiety (UKB data field 20541) 39,704 European ancestry cases, 2,474 European ancestry controls NA Affymetrix, Illumina [85324] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078632 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nicorandil (Gene-based burden) 1,420 European ancestry cases, 319,338 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082127 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Worried most days during period of worst anxiety (UKB data field 20538) 36,918 European ancestry cases, 4,895 European ancestry controls NA Affymetrix, Illumina [84623] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078626 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - nifedipine (Gene-based burden) 1,016 European ancestry cases, 319,742 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081988 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple worries during worst period of anxiety (UKB data field 20540) 31,523 European ancestry cases, 10,086 European ancestry controls NA Affymetrix, Illumina [84266] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078631 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - olanzapine (Gene-based burden) 501 European ancestry cases, 320,257 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082157 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty concentrating during worst period of anxiety (UKB data field 20419) 31,317 European ancestry cases, 10,080 European ancestry controls NA Affymetrix, Illumina [83878] 0 decreased concentration http://purl.obolibrary.org/obo/PATO_0001163 GCST90078438 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - olmesartan (Gene-based burden) 532 European ancestry cases, 320,226 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082215 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Keyed up or on edge during worst period of anxiety (UKB data field 20423) 32,732 European ancestry cases, 8,568 European ancestry controls NA Affymetrix, Illumina [83761] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90078441 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - omacor (Gene-based burden) 566 European ancestry cases, 320,192 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082203 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of breast (UKB data field 40006) 2,316 European ancestry cases, 38,689 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90079129 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - omega 3 fish oil supplement (Gene-based burden) 17,260 European ancestry cases, 303,498 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082221 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of cervix uteri (UKB data field 40006) 3,495 European ancestry cases, 37,510 European ancestry controls NA Affymetrix, Illumina [83254] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90079131 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - omeprazole (Gene-based burden) 28,675 European ancestry cases, 292,083 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082018 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of cervix, unspecified (UKB data field 40006) 2,999 European ancestry cases, 38,006 European ancestry controls NA Affymetrix, Illumina [83254] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90079130 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - orlistat (Gene-based burden) 512 European ancestry cases, 320,246 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082187 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraductal carcinoma in situ of breast (UKB data field 40006) 1,947 European ancestry cases, 39,058 European ancestry controls NA Affymetrix, Illumina [83254] 0 Ductal Breast Carcinoma In Situ and Lobular Carcinoma In Situ http://www.ebi.ac.uk/efo/EFO_1000221 GCST90079128 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - oxybutynin (Gene-based burden) 1,071 European ancestry cases, 319,687 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082096 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of breast (UKB data field 40006) 12,472 European ancestry cases, 28,533 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90079108 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - oxytetracycline (Gene-based burden) 1,287 European ancestry cases, 319,471 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082056 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of breast of unspecified site (UKB data field 40006) 5,931 European ancestry cases, 35,074 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90079107 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pantoprazole (Gene-based burden) 843 European ancestry cases, 319,915 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082158 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of corpus uteri (UKB data field 40006) 1,612 European ancestry cases, 39,393 European ancestry controls 1,141 European ancestry cases, 122,694 European ancestry controls Affymetrix, Illumina [83254] 0 uterine corpus cancer http://www.ebi.ac.uk/efo/EFO_0007532 GCST90079110 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - paracetamol (Gene-based burden) 83,776 European ancestry cases, 236,982 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082227 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of endometrium (UKB data field 40006) 1,536 European ancestry cases, 39,469 European ancestry controls NA Affymetrix, Illumina [83254] 0 endometrial cancer http://purl.obolibrary.org/obo/MONDO_0011962 GCST90079109 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian right (UKB data field 5098) 90,887 European ancestry individuals NA Affymetrix, Illumina [169291] 2 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079275 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeplessness insomnia - Sometimes (UKB data field 1200) (Gene-based burden) 213,925 European ancestry cases, 216,502 European ancestry controls NA Illumina [185942] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90081564 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm right 90,887 European ancestry individuals NA Affymetrix, Illumina [169291] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081483 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeplessness insomnia - Usually (UKB data field 1200) (Gene-based burden) 130,457 European ancestry cases, 299,970 European ancestry controls NA Illumina [185942] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90081565 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power angle right (UKB data field 5114) 90,862 European ancestry individuals NA Affymetrix, Illumina [169256] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079292 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking status - Current (UKB data field 20116) (Gene-based burden) 45,239 European ancestry cases, 384,016 European ancestry controls NA Illumina [185928] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90082288 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power left (UKB data field 5118) 89,735 European ancestry individuals NA Affymetrix, Illumina [167455] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079296 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking status - Never (UKB data field 20116) (Gene-based burden) 232,790 European ancestry cases, 196,465 European ancestry controls NA Illumina [185928] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90082286 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian angle left (UKB data field 5105) 89,735 European ancestry individuals NA Affymetrix, Illumina [167455] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079283 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Smoking status - Previous (UKB data field 20116) (Gene-based burden) 155,124 European ancestry cases, 274,131 European ancestry controls NA Illumina [185928] 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90082287 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian left (UKB data field 5134) 89,735 European ancestry individuals NA Affymetrix, Illumina [167455] 2 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079300 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Snoring (UKB data field 1210) (Gene-based burden) 154,235 European ancestry cases, 248,326 European ancestry controls NA Illumina [185502] 0 Snoring http://purl.obolibrary.org/obo/HP_0025267 GCST90081566 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian angle left (UKB data field 5102) 89,735 European ancestry individuals NA Affymetrix, Illumina [167455] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079280 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Shortness of breath walking on level ground (UKB data field 4717) (Gene-based burden) 18,321 European ancestry cases, 156,558 European ancestry controls NA Illumina [176899] 0 shortness of breath http://www.ebi.ac.uk/efo/EFO_0009727 GCST90083203 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian left (UKB data field 5097) 89,735 European ancestry individuals NA Affymetrix, Illumina [167455] 3 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079274 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sodium in urine (UKB data field 30530) (Gene-based burden) 418,293 European ancestry individuals NA Illumina [185792] 0 sodium measurement http://www.ebi.ac.uk/efo/EFO_0009282 GCST90082996 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm left 89,735 European ancestry individuals NA Affymetrix, Illumina [167455] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081482 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speech reception threshold estimate left (UKB data field 20019) (Gene-based burden) 170,543 European ancestry individuals NA Illumina [176396] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90082235 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power angle left (UKB data field 5113) 89,706 European ancestry individuals NA Affymetrix, Illumina [167414] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079291 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speech reception threshold estimate right (UKB data field 20021) (Gene-based burden) 170,510 European ancestry individuals NA Illumina [176412] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90082236 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hay fever rhinitis or eczema (age of onset) (UKB data field 3761) 88,602 European ancestry individuals NA Affymetrix, Illumina [165193] 1 atopic eczema, age of onset of allergic disease http://www.ebi.ac.uk/efo/EFO_0000274, http://purl.obolibrary.org/obo/OBA_2001017 GCST90079072 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of onset of IBS symptoms - 801 Started suddenly (UKB data field 21070) (Gene-based burden) 4,336 European ancestry cases, 9,842 European ancestry controls NA Illumina [92007] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90082819 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Headaches for three months (UKB data field 3799) 40,144 European ancestry cases, 47,613 European ancestry controls NA Affymetrix, Illumina [164284] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90079074 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of onset of IBS symptoms - 802 Came on gradually (UKB data field 21070) (Gene-based burden) 9,842 European ancestry cases, 4,336 European ancestry controls NA Illumina [92007] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90082820 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Abdominal discomfort pain for 6 months or longer (UKB data field 21027) 43,558 European ancestry cases, 39,720 European ancestry controls NA Affymetrix, Illumina [156499] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90078696 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rodent ulcer (UKB data field 20001) (Gene-based burden) 956 European ancestry cases, 38,658 European ancestry controls NA Illumina [134284] 0 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90081629 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level left - normal (UKB data field 5155) 99,415 European ancestry cases, 1,888 European ancestry controls NA Affymetrix, Illumina [185823] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079308 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin cancer (UKB data field 20001) (Gene-based burden) 1,556 European ancestry cases, 38,058 European ancestry controls NA Illumina [134284] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90081613 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index left (UKB data field 5156) 101,303 European ancestry individuals NA Affymetrix, Illumina [185823] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079311 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Squamous cell carcinoma (UKB data field 20001) (Gene-based burden) 638 European ancestry cases, 38,976 European ancestry controls NA Illumina [134284] 0 squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707 GCST90081627 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain problems during intercourse in the last three months - 600 Not bothered at all (UKB data field 21057) 81,222 European ancestry cases, 19,703 European ancestry controls NA Affymetrix, Illumina [184440] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078811 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Testicular cancer (UKB data field 20001) (Gene-based burden) 769 European ancestry cases, 38,845 European ancestry controls NA Illumina [134263] 0 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST90081622 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain problems during intercourse in the last three months - 601 Bothered a little (UKB data field 21057) 14,178 European ancestry cases, 86,747 European ancestry controls NA Affymetrix, Illumina [184440] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078812 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Uterine endometrial cancer (UKB data field 20001) (Gene-based burden) 1,131 European ancestry cases, 38,483 European ancestry controls NA Illumina [134284] 0 uterine carcinoma http://www.ebi.ac.uk/efo/EFO_0002919 GCST90081619 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain problems during intercourse in the last three months - 602 Bothered a lot (UKB data field 21057) 5,525 European ancestry cases, 95,400 European ancestry controls NA Affymetrix, Illumina [184440] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078813 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sensitive stomach (UKB data field 21064) (Gene-based burden) 32,677 European ancestry cases, 109,193 European ancestry controls NA Illumina [172201] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90082814 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interval between previous point and current one in alphanumeric path trail 2 (UKB data field 20155) 98,260 European ancestry individuals NA Affymetrix, Illumina [180604] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078321 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sensitivity hurt feelings (UKB data field 1950) (Gene-based burden) 236,796 European ancestry cases, 182,655 European ancestry controls NA Illumina [185779] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90081607 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 25 (UKB data field 5012) 12,040 European ancestry cases, 86,030 European ancestry controls NA Affymetrix, Illumina [180063] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079260 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 1 (UKB data field 21039) (Gene-based burden) 2,871 European ancestry cases, 33,070 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082741 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 26 (UKB data field 5012) 76,054 European ancestry cases, 22,016 European ancestry controls NA Affymetrix, Illumina [180063] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079261 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 2 (UKB data field 21039) (Gene-based burden) 5,695 European ancestry cases, 30,246 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082742 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 27 (UKB data field 5012) 5,087 European ancestry cases, 92,983 European ancestry controls NA Affymetrix, Illumina [180063] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079262 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 3 (UKB data field 21039) (Gene-based burden) 5,965 European ancestry cases, 29,976 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082743 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 28 (UKB data field 5012) 2,954 European ancestry cases, 95,116 European ancestry controls NA Affymetrix, Illumina [180063] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079263 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 4 (UKB data field 21039) (Gene-based burden) 4,032 European ancestry cases, 31,909 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082744 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 29 (UKB data field 5012) 4,869 European ancestry cases, 93,201 European ancestry controls NA Affymetrix, Illumina [180063] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079264 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 5 (UKB data field 21039) (Gene-based burden) 5,472 European ancestry cases, 30,469 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082745 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Knee pain for three months (UKB data field 3773) 76,543 European ancestry cases, 20,879 European ancestry controls NA Affymetrix, Illumina [178309] 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90079073 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 6 (UKB data field 21039) (Gene-based burden) 3,970 European ancestry cases, 31,971 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082746 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 502 Often (UKB data field 21032) 5,831 European ancestry cases, 77,315 European ancestry controls NA Affymetrix, Illumina [156301] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078719 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD SR: Ankylosing spondylitis - B27 negative (Gene-based burden) 761 European ancestry cases, 355,581 European ancestry controls NA Illumina [184799] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90083519 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 503 Most of the time (UKB data field 21032) 4,007 European ancestry cases, 79,139 European ancestry controls NA Affymetrix, Illumina [156301] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078720 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD SR: Ankylosing spondylitis - B27 positive (Gene-based burden) 715 European ancestry cases, 30,652 European ancestry controls NA Illumina [125055] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90083520 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 504 Always (UKB data field 21032) 1,280 European ancestry cases, 81,866 European ancestry controls NA Affymetrix, Illumina [156301] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078721 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD M45: Ankylosing spondylitis (Gene-based burden) 848 European ancestry cases, 386,233 European ancestry controls NA Illumina [185325] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90083522 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 500 Never (UKB data field 21028) 12,998 European ancestry cases, 70,103 European ancestry controls NA Affymetrix, Illumina [156270] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078697 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Standard deviation of acceleration (UKB data field 90013) (Gene-based burden) 91,770 European ancestry individuals NA Illumina [161846] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083493 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 501 Sometimes (UKB data field 21028) 22,792 European ancestry cases, 60,309 European ancestry controls NA Affymetrix, Illumina [156270] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078698 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Standing height (UKB data field 50) (Gene-based burden) 430,070 European ancestry individuals NA Illumina [185930] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90083263 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 502 Often (UKB data field 21028) 9,192 European ancestry cases, 73,909 European ancestry controls NA Affymetrix, Illumina [156270] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078699 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Started insulin within one year diabetes mellitis diagnosis (UKB data field 2986) (Gene-based burden) 2,491 European ancestry cases, 18,545 European ancestry controls NA Illumina [109435] 0 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90082963 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 503 Most of the time (UKB data field 21028) 22,017 European ancestry cases, 61,084 European ancestry controls NA Affymetrix, Illumina [156270] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078700 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Started wearing glasses or contacts after 40 (Gene-based burden) 182,074 European ancestry individuals NA Illumina [176741] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085527 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 504 Always (UKB data field 21028) 16,102 European ancestry cases, 66,999 European ancestry controls NA Affymetrix, Illumina [156270] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90078701 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Started wearing glasses or contacts before 40 (Gene-based burden) 192,090 European ancestry individuals NA Illumina [178208] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085528 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 500 Never (UKB data field 21030) 49,036 European ancestry cases, 34,033 European ancestry controls NA Affymetrix, Illumina [156155] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078707 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stomach abdominal pain for three months (UKB data field 3741) (Gene-based burden) 21,293 European ancestry cases, 16,808 European ancestry controls NA Illumina [134210] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90083056 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 501 Sometimes (UKB data field 21030) 24,863 European ancestry cases, 58,206 European ancestry controls NA Affymetrix, Illumina [156155] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078708 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 500 Never (UKB data field 21031) (Gene-based burden) 28,122 European ancestry cases, 55,054 European ancestry controls NA Illumina [159654] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082698 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 502 Often (UKB data field 21030) 3,613 European ancestry cases, 79,456 European ancestry controls NA Affymetrix, Illumina [156155] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078709 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 501 Sometimes (UKB data field 21031) (Gene-based burden) 31,226 European ancestry cases, 51,950 European ancestry controls NA Illumina [159654] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082699 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 503 Most of the time (UKB data field 21030) 4,053 European ancestry cases, 79,016 European ancestry controls NA Affymetrix, Illumina [156155] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078710 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 502 Often (UKB data field 21031) (Gene-based burden) 9,184 European ancestry cases, 73,992 European ancestry controls NA Illumina [159654] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082700 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Less frequent bowel movements when abdominal discomfort pain started - 504 Always (UKB data field 21030) 1,504 European ancestry cases, 81,565 European ancestry controls NA Affymetrix, Illumina [156155] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078711 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - No category, ECG not to be done (UKB data field 6024) 1,253 European ancestry cases, 80,450 European ancestry controls NA Affymetrix, Illumina [154752] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079417 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Surgery on leg arteries other than for varicose veins (UKB data field 5529) (Gene-based burden) 1,424 European ancestry cases, 38,914 European ancestry controls NA Illumina [136290] 0 surgery on leg artery http://www.ebi.ac.uk/efo/EFO_0009729 GCST90083346 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Retinal optical coherence tomography - duration at which OCT screen shown left (UKB data field 6073) 81,113 European ancestry individuals NA Affymetrix, Illumina [153728] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079422 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit completion status - Abandoned (UKB data field 20245) (Gene-based burden) 2,095 European ancestry cases, 104,769 European ancestry controls NA Illumina [166140] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082368 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Doctor restricts physical activity due to heart condition (UKB data field 6014) 3,441 European ancestry cases, 77,630 European ancestry controls NA Affymetrix, Illumina [153701] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079405 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit completion status - Completed (UKB data field 20245) (Gene-based burden) 102,495 European ancestry cases, 4,369 European ancestry controls NA Illumina [166140] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082367 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain felt outside physical activity (UKB data field 6016) 2,532 European ancestry cases, 78,491 European ancestry controls NA Affymetrix, Illumina [153619] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90079407 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit completion status - Completed with pause (UKB data field 20245) (Gene-based burden) 2,274 European ancestry cases, 104,590 European ancestry controls NA Illumina [166140] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082369 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Completion status of test - Fully completed (UKB data field 6020) 74,782 European ancestry cases, 5,739 European ancestry controls NA Affymetrix, Illumina [152780] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079409 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Systolic blood pressure automated reading (UKB data field 4080) (Gene-based burden) 408,211 European ancestry individuals NA Illumina [185723] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90083132 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Completion status of test - Participant wanted to stop early (UKB data field 6020) 814 European ancestry cases, 79,707 European ancestry controls NA Affymetrix, Illumina [152780] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079410 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Toxoplasma gondii (UKB data field 23062) (Gene-based burden) 2,347 European ancestry cases, 6,194 European ancestry controls NA Illumina [70714] 0 Toxoplasma gondii seropositivity http://www.ebi.ac.uk/efo/EFO_0007047 GCST90082879 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Completion status of test - Heart rate reached safety level (UKB data field 6020) 4,620 European ancestry cases, 75,901 European ancestry controls NA Affymetrix, Illumina [152780] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079411 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes Nephropathy Loose (Gene-based burden) 2,067 European ancestry cases, 23,543 European ancestry controls NA Illumina [117999] 0 type 2 diabetes nephropathy http://www.ebi.ac.uk/efo/EFO_0004997 GCST90085500 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - Number of trend entries (UKB data field 6038) 80,512 European ancestry individuals NA Affymetrix, Illumina [152764] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079421 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes Neuropathy (Gene-based burden) 751 European ancestry cases, 25,077 European ancestry controls NA Illumina [118296] 0 type 2 diabetes nephropathy http://www.ebi.ac.uk/efo/EFO_0004997 GCST90085501 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Target heart rate achieved (UKB data field 6034) 8,718 European ancestry cases, 71,794 European ancestry controls NA Affymetrix, Illumina [152764] 0 achievement of target heart rate, self-reported http://www.ebi.ac.uk/efo/EFO_0009823 GCST90079420 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes New (Gene-based burden) 30,259 European ancestry cases, 355,886 European ancestry controls NA Illumina [185319] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90085502 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum workload during fitness test (UKB data field 6032) 80,511 European ancestry individuals NA Affymetrix, Illumina [152762] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079418 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes New Strict (Gene-based burden) 11,970 European ancestry cases, 340,301 European ancestry controls NA Illumina [184718] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90085503 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum heart rate during fitness test (UKB data field 6033) 80,492 European ancestry individuals NA Affymetrix, Illumina [152731] 0 heart rate response to exercise http://www.ebi.ac.uk/efo/EFO_0009184 GCST90079419 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes Ophthalmopathy (Gene-based burden) 4,180 European ancestry cases, 21,737 European ancestry controls NA Illumina [118476] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90085504 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain felt during physical activity (UKB data field 6015) 2,964 European ancestry cases, 77,501 European ancestry controls NA Affymetrix, Illumina [152702] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90079406 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bleed (Gene-based burden) 49,682 European ancestry cases, 178,676 European ancestry controls NA Illumina [180923] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90085505 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG heart rate (UKB data field 5983) 80,260 European ancestry individuals NA Affymetrix, Illumina [152339] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90079404 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of sound through heel (UKB data field 3146) (Gene-based burden) 246,319 European ancestry individuals NA Illumina [181011] 0 velocity of sound measurement http://www.ebi.ac.uk/efo/EFO_0005654 GCST90083036 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 500 Never (UKB data field 21031) 28,122 European ancestry cases, 55,054 European ancestry controls NA Affymetrix, Illumina [156329] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078712 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of sound through heel left (UKB data field 4103) (Gene-based burden) 166,283 European ancestry individuals NA Illumina [176191] 0 velocity of sound measurement http://www.ebi.ac.uk/efo/EFO_0005654 GCST90083136 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 501 Sometimes (UKB data field 21031) 31,226 European ancestry cases, 51,950 European ancestry controls NA Affymetrix, Illumina [156329] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078713 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Speed of sound through heel right (UKB data field 4122) (Gene-based burden) 166,358 European ancestry individuals NA Illumina [176168] 0 velocity of sound measurement http://www.ebi.ac.uk/efo/EFO_0005654 GCST90083142 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 502 Often (UKB data field 21031) 9,184 European ancestry cases, 73,992 European ancestry controls NA Affymetrix, Illumina [156329] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078714 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical power left (UKB data field 5085) (Gene-based burden) 107,117 European ancestry individuals NA Illumina [167449] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083254 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 503 Most of the time (UKB data field 21031) 8,883 European ancestry cases, 74,293 European ancestry controls NA Affymetrix, Illumina [156329] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078715 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical power right (UKB data field 5084) (Gene-based burden) 107,475 European ancestry individuals NA Illumina [167589] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083253 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 504 Always (UKB data field 21031) 5,761 European ancestry cases, 77,415 European ancestry controls NA Affymetrix, Illumina [156329] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078716 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent left (first instance) (Gene-based burden) 93,665 European ancestry individuals NA Illumina [164426] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085494 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 500 Never (UKB data field 21029) 34,465 European ancestry cases, 48,678 European ancestry controls NA Affymetrix, Illumina [156306] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078702 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent right (first instance) (Gene-based burden) 93,958 European ancestry individuals NA Illumina [164523] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085495 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 501 Sometimes (UKB data field 21029) 29,974 European ancestry cases, 53,169 European ancestry controls NA Affymetrix, Illumina [156306] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078703 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent left (Gene-based burden) 107,117 European ancestry individuals NA Illumina [167449] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085496 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 502 Often (UKB data field 21029) 6,273 European ancestry cases, 76,870 European ancestry controls NA Affymetrix, Illumina [156306] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078704 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent left - started wearing glasses contacts before 40 (Gene-based burden) 48,821 European ancestry individuals NA Illumina [143799] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085497 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 503 Most of the time (UKB data field 21029) 8,200 European ancestry cases, 74,943 European ancestry controls NA Affymetrix, Illumina [156306] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078705 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent right (Gene-based burden) 107,475 European ancestry individuals NA Illumina [167589] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085498 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More frequent bowel movements when abdominal discomfort pain started - 504 Always (UKB data field 21029) 4,231 European ancestry cases, 78,912 European ancestry controls NA Affymetrix, Illumina [156306] 0 bowel dysfunction http://purl.obolibrary.org/obo/MONDO_0004880 GCST90078706 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent right - started wearing glasses contacts before 40 (Gene-based burden) 48,976 European ancestry individuals NA Illumina [143890] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90085499 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 500 Never (UKB data field 21032) 41,782 European ancestry cases, 41,364 European ancestry controls NA Affymetrix, Illumina [156301] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078717 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD M45: Ankylosing spondylitis - B27 positive (Gene-based burden) 526 European ancestry cases, 30,652 European ancestry controls NA Illumina [124840] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90083518 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 501 Sometimes (UKB data field 21032) 30,246 European ancestry cases, 52,900 European ancestry controls NA Affymetrix, Illumina [156301] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90078718 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD SR: Ankylosing spondylitis (Gene-based burden) 1,476 European ancestry cases, 386,233 European ancestry controls NA Illumina [185336] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90083521 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 9 (UKB data field 21036) (Gene-based burden) 792 European ancestry cases, 44,149 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082727 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean spherical equivalent (first instance) 93,186 European ancestry individuals NA Affymetrix, Illumina [174239] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081496 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of manic irritable episodes - No problems (UKB data field 5674) (Gene-based burden) 22,910 European ancestry cases, 8,213 European ancestry controls NA Illumina [126878] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083356 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Refractive astigmatism (first instance) 93,186 European ancestry individuals NA Affymetrix, Illumina [174239] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90081505 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of manic irritable episodes - Needed treatment or caused problems with work relationships finances the law or other aspects of life (UKB data field 5674) (Gene-based burden) 8,512 European ancestry cases, 22,611 European ancestry controls NA Illumina [126878] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90083357 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration to complete numeric path trail 1 (UKB data field 20156) 92,687 European ancestry individuals NA Affymetrix, Illumina [171767] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078322 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of problems due to mania or irritability - Needed treatment or caused problems with work relationships finances the law or other aspects of life (UKB data field 20493) (Gene-based burden) 9,482 European ancestry cases, 22,464 European ancestry controls NA Illumina [126797] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90082520 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration to complete alphanumeric path trail 2 (UKB data field 20157) 92,685 European ancestry individuals NA Affymetrix, Illumina [171763] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078323 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sex hormone binding globulin levels (UKB data field 30830) (Gene-based burden) 374,810 European ancestry individuals NA Illumina [185052] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90083026 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm left (first instance) 90,788 European ancestry individuals NA Affymetrix, Illumina [170397] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081474 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sitting height (UKB data field 20015) (Gene-based burden) 430,080 European ancestry individuals NA Illumina [185928] 0 sitting height measurement http://www.ebi.ac.uk/efo/EFO_0011011 GCST90082231 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm right (first instance) 90,792 European ancestry individuals NA Affymetrix, Illumina [170358] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081475 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Brown (UKB data field 1717) (Gene-based burden) 2,065 European ancestry cases, 423,296 European ancestry controls NA Illumina [185861] 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90081587 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overall acceleration average (UKB data field 90012) 91,770 European ancestry individuals NA Affymetrix, Illumina [170065] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079506 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Dark olive (UKB data field 1717) (Gene-based burden) 7,210 European ancestry cases, 418,151 European ancestry controls NA Illumina [185861] 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90081586 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Standard deviation of acceleration (UKB data field 90013) 91,770 European ancestry individuals NA Affymetrix, Illumina [170065] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079507 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Fair (UKB data field 1717) (Gene-based burden) 304,034 European ancestry cases, 121,327 European ancestry controls NA Illumina [185861] 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90081584 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm cylindrical power right (UKB data field 5117) 90,887 European ancestry individuals NA Affymetrix, Illumina [169291] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079295 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Light olive (UKB data field 1717) (Gene-based burden) 80,996 European ancestry cases, 344,365 European ancestry controls NA Illumina [185861] 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90081585 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian angle right (UKB data field 5106) 90,887 European ancestry individuals NA Affymetrix, Illumina [169291] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079284 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin colour - Very fair (UKB data field 1717) (Gene-based burden) 35,374 European ancestry cases, 389,987 European ancestry controls NA Illumina [185861] 0 skin pigmentation http://www.ebi.ac.uk/efo/EFO_0003784 GCST90081583 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm strong meridian right (UKB data field 5133) 90,887 European ancestry individuals NA Affymetrix, Illumina [169291] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079299 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeping too much (UKB data field 20534) (Gene-based burden) 11,243 European ancestry cases, 42,867 European ancestry controls NA Illumina [146002] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90082602 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm weak meridian angle right (UKB data field 5101) 90,887 European ancestry individuals NA Affymetrix, Illumina [169291] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079279 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeplessness insomnia - Never rarely (UKB data field 1200) (Gene-based burden) 107,304 European ancestry cases, 323,123 European ancestry controls NA Illumina [185942] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90081563 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 503 Most of the time (UKB data field 21031) (Gene-based burden) 8,883 European ancestry cases, 74,293 European ancestry controls NA Illumina [159654] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082701 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hormone replacement therapy use (age of onset) (UKB data field 3536) 83,509 European ancestry individuals NA Affymetrix, Illumina [156014] 0 age at onset, hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90079061 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stools looser when abdominal discomfort pain started - 504 Always (UKB data field 21031) (Gene-based burden) 5,761 European ancestry cases, 77,415 European ancestry controls NA Illumina [159654] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082702 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required right - elsewhere (UKB data field 6074) 4,185 European ancestry cases, 77,665 European ancestry controls NA Affymetrix, Illumina [154921] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079425 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stronger worrying than other people during period of worst anxiety (UKB data field 20542) (Gene-based burden) 24,579 European ancestry cases, 5,218 European ancestry controls NA Illumina [123339] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082619 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required right - none (UKB data field 6074) 32,052 European ancestry cases, 49,798 European ancestry controls NA Affymetrix, Illumina [154921] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079423 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substance of prescription or over the counter medication addiction - A sedative benzodiazepine or sleeping tablet (UKB data field 20551) (Gene-based burden) 526 European ancestry cases, 631 European ancestry controls NA Illumina [13674] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082651 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required right - wearing (UKB data field 6074) 46,020 European ancestry cases, 35,830 European ancestry controls NA Affymetrix, Illumina [154921] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079424 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for anxiety - Drugs or alcohol more than once (UKB data field 20549) (Gene-based burden) 7,444 European ancestry cases, 16,129 European ancestry controls NA Illumina [113352] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082648 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required left - elsewhere (UKB data field 6075) 4,188 European ancestry cases, 77,628 European ancestry controls NA Affymetrix, Illumina [154846] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079428 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for anxiety - Medication prescribed to you for at least two weeks (UKB data field 20549) (Gene-based burden) 17,819 European ancestry cases, 5,754 European ancestry controls NA Illumina [113352] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082647 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required left - none (UKB data field 6075) 32,050 European ancestry cases, 49,766 European ancestry controls NA Affymetrix, Illumina [154846] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079426 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for anxiety - Unprescribed medication more than once (UKB data field 20549) (Gene-based burden) 3,611 European ancestry cases, 19,962 European ancestry controls NA Illumina [113352] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082646 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required left - wearing (UKB data field 6075) 45,986 European ancestry cases, 35,830 European ancestry controls NA Affymetrix, Illumina [154846] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079427 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for depression - Drugs or alcohol more than once (UKB data field 20546) (Gene-based burden) 10,129 European ancestry cases, 30,541 European ancestry controls NA Illumina [135346] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082635 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise duration (UKB data field 6022) 81,703 European ancestry individuals NA Affymetrix, Illumina [154752] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079412 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for depression - Medication prescribed to you for at least two weeks (UKB data field 20546) (Gene-based burden) 33,619 European ancestry cases, 7,051 European ancestry controls NA Illumina [135346] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082634 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - cycle rising to 50 level (UKB data field 6024) 61,060 European ancestry cases, 20,643 European ancestry controls NA Affymetrix, Illumina [154752] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079413 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for depression - Unprescribed medication more than once (UKB data field 20546) (Gene-based burden) 4,881 European ancestry cases, 35,789 European ancestry controls NA Illumina [135346] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082633 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - cycle rising to 35 level (UKB data field 6024) 9,643 European ancestry cases, 72,060 European ancestry controls NA Affymetrix, Illumina [154752] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079414 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Suffer from nerves (UKB data field 2010) (Gene-based burden) 91,369 European ancestry cases, 324,851 European ancestry controls NA Illumina [185754] 0 feeling nervous measurement http://www.ebi.ac.uk/efo/EFO_0009597 GCST90082254 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - cycle at constant level (UKB data field 6024) 2,320 European ancestry cases, 79,383 European ancestry controls NA Affymetrix, Illumina [154752] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079415 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Summed Metabolic Equivalent Task - minutes per week for all activity (UKB data field 22040) (Gene-based burden) 349,393 European ancestry individuals NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082845 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise - at rest measurement (UKB data field 6024) 8,201 European ancestry cases, 73,502 European ancestry controls NA Affymetrix, Illumina [154752] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90079416 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - Summed minutes activity (UKB data field 22034) (Gene-based burden) 349,393 European ancestry individuals NA Illumina [184553] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90082840 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Paternal age (UKB data field 2946) 96,287 European ancestry individuals NA Affymetrix, Illumina [178308] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90078974 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 7 (UKB data field 21039) (Gene-based burden) 3,790 European ancestry cases, 32,151 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082747 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 68 (UKB data field 20175) 646 European ancestry cases, 95,556 European ancestry controls NA Affymetrix, Illumina [177071] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078345 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 8 (UKB data field 21039) (Gene-based burden) 2,410 European ancestry cases, 33,531 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082748 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 69 (UKB data field 20175) 72,471 European ancestry cases, 23,731 European ancestry controls NA Affymetrix, Illumina [177071] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078346 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 9 (UKB data field 21039) (Gene-based burden) 896 European ancestry cases, 35,045 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082749 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 70 (UKB data field 20175) 20,903 European ancestry cases, 75,299 European ancestry controls NA Affymetrix, Illumina [177071] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078347 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 10 - Very severe distension (UKB data field 21039) (Gene-based burden) 572 European ancestry cases, 35,369 European ancestry controls NA Illumina [130824] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90082740 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 71 (UKB data field 20175) 1,122 European ancestry cases, 95,080 European ancestry controls NA Affymetrix, Illumina [177071] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078348 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 1 (UKB data field 21036) (Gene-based burden) 4,633 European ancestry cases, 40,308 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082719 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 72 (UKB data field 20175) 1,060 European ancestry cases, 95,142 European ancestry controls NA Affymetrix, Illumina [177071] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078349 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 2 (UKB data field 21036) (Gene-based burden) 8,224 European ancestry cases, 36,717 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082720 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - mean spherical equivalent (UKB data field 20261) 94,332 European ancestry individuals NA Affymetrix, Illumina [176054] 1 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90078391 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 3 (UKB data field 21036) (Gene-based burden) 7,955 European ancestry cases, 36,986 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082721 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia diagnosis - highly myopic (UKB data field 20262) 3,753 European ancestry cases, 90,579 European ancestry controls NA Affymetrix, Illumina [176054] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90078394 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 4 (UKB data field 21036) (Gene-based burden) 4,900 European ancestry cases, 40,041 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082722 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia diagnosis - moderate low myopia (UKB data field 20262) 24,937 European ancestry cases, 69,395 European ancestry controls NA Affymetrix, Illumina [176054] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90078393 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 5 (UKB data field 21036) (Gene-based burden) 5,756 European ancestry cases, 39,185 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082723 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia diagnosis - non myopic (UKB data field 20262) 65,642 European ancestry cases, 28,690 European ancestry controls NA Affymetrix, Illumina [176054] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078392 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 6 (UKB data field 21036) (Gene-based burden) 4,639 European ancestry cases, 40,302 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082724 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent right (first instance) 93,958 European ancestry individuals NA Affymetrix, Illumina [175455] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081509 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 7 (UKB data field 21036) (Gene-based burden) 4,551 European ancestry cases, 40,390 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082725 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spherical equivalent left (first instance) 93,665 European ancestry individuals NA Affymetrix, Illumina [175002] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081508 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal pain - 8 (UKB data field 21036) (Gene-based burden) 2,679 European ancestry cases, 42,262 European ancestry controls NA Illumina [139515] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90082726 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anisometropia (first instance) 93,186 European ancestry individuals NA Affymetrix, Illumina [174239] 0 Anisometropia http://purl.obolibrary.org/obo/HP_0012803 GCST90081452 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Basal cell carcinoma (UKB data field 20001) 4,723 European ancestry cases, 34,891 European ancestry controls NA Affymetrix, Illumina [80688] 0 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90077640 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - risedronate sodium (Gene-based burden) 928 European ancestry cases, 319,830 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082193 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bladder cancer (UKB data field 20001) 1,128 European ancestry cases, 38,486 European ancestry controls NA Affymetrix, Illumina [80688] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90077631 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rosiglitazone (Gene-based burden) 601 European ancestry cases, 320,157 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082198 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cervical cancer (UKB data field 20001) 1,786 European ancestry cases, 37,828 European ancestry controls NA Affymetrix, Illumina [80688] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90077634 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rosuvastatin (Gene-based burden) 2,905 European ancestry cases, 317,853 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082211 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. CIN pre cancer cells cervix (UKB data field 20001) 1,872 European ancestry cases, 37,742 European ancestry controls NA Affymetrix, Illumina [80688] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90077642 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salamol inhaler (Gene-based burden) 1,374 European ancestry cases, 319,384 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081997 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Colon cancer / sigmoid cancer (UKB data field 20001) 1,445 European ancestry cases, 38,169 European ancestry controls NA Affymetrix, Illumina [80688] 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90077629 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salbutamol (Gene-based burden) 5,488 European ancestry cases, 315,270 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082087 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Kidney / renal cell cancer (UKB data field 20001) 600 European ancestry cases, 39,014 European ancestry controls NA Affymetrix, Illumina [80688] 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90077630 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salbutamol spacehaler (Gene-based burden) 2,981 European ancestry cases, 317,777 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082153 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Large bowel cancer / colorectal cancer (UKB data field 20001) 662 European ancestry cases, 38,952 European ancestry controls NA Affymetrix, Illumina [80688] 0 colorectal carcinoma http://www.ebi.ac.uk/efo/EFO_1001951 GCST90077628 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salbutamol product (Gene-based burden) 692 European ancestry cases, 320,066 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082175 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma (UKB data field 20001) 3,595 European ancestry cases, 36,019 European ancestry controls NA Affymetrix, Illumina [80688] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90077638 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salmeterol (Gene-based burden) 1,161 European ancestry cases, 319,597 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081998 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non hodgkins lymphoma (UKB data field 20001) 885 European ancestry cases, 38,729 European ancestry controls NA Affymetrix, Illumina [80688] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90077637 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - salmeterol fluticasone propionate (Gene-based burden) 814 European ancestry cases, 319,944 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082178 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non melanoma skin cancer (UKB data field 20001) 717 European ancestry cases, 38,897 European ancestry controls NA Affymetrix, Illumina [80688] 0 non-melanoma skin carcinoma http://www.ebi.ac.uk/efo/EFO_0009260 GCST90077639 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - selenium ace tablet (Gene-based burden) 581 European ancestry cases, 320,177 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082130 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ovarian cancer (UKB data field 20001) 769 European ancestry cases, 38,845 European ancestry controls NA Affymetrix, Illumina [80688] 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90077632 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - selenium product (Gene-based burden) 1,390 European ancestry cases, 319,368 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082098 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rodent ulcer (UKB data field 20001) 956 European ancestry cases, 38,658 European ancestry controls NA Affymetrix, Illumina [80688] 0 basal cell carcinoma http://www.ebi.ac.uk/efo/EFO_0004193 GCST90077643 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - senna (Gene-based burden) 874 European ancestry cases, 319,884 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082019 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Skin cancer (UKB data field 20001) 1,556 European ancestry cases, 38,058 European ancestry controls NA Affymetrix, Illumina [80688] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90077627 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of ovary (UKB data field 40006) 1,106 European ancestry cases, 39,899 European ancestry controls NA Affymetrix, Illumina [83254] 0 ovarian neoplasm http://www.ebi.ac.uk/efo/EFO_0003893 GCST90079111 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - piriton (Gene-based burden) 684 European ancestry cases, 320,074 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082005 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of overlapping sites of breast (UKB data field 40006) 878 European ancestry cases, 40,127 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079106 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pizotifen (Gene-based burden) 662 European ancestry cases, 320,096 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082097 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of upper-inner quadrant of breast (UKB data field 40006) 1,025 European ancestry cases, 39,980 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079102 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pravastatin (Gene-based burden) 2,500 European ancestry cases, 318,258 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082118 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of upper-outer quadrant of breast (UKB data field 40006) 3,434 European ancestry cases, 37,571 European ancestry controls NA Affymetrix, Illumina [83254] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90079104 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prednisolone (Gene-based burden) 2,671 European ancestry cases, 318,087 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082062 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to illicit or recreational drugs (UKB data field 20456) 654 European ancestry cases, 7,551 European ancestry controls NA Affymetrix, Illumina [21175] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90078480 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Waist circumference (UKB data field 48) (Gene-based burden) 430,261 European ancestry individuals NA Illumina [185938] 0 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90083214 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to prescription or over the counter medication (UKB data field 20503) 1,162 European ancestry cases, 7,018 European ancestry controls NA Affymetrix, Illumina [21132] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90078558 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Waking too early (UKB data field 20535) (Gene-based burden) 41,019 European ancestry cases, 13,091 European ancestry controls NA Illumina [146002] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90082603 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to a behaviour or miscellanous (UKB data field 20431) 1,959 European ancestry cases, 6,226 European ancestry controls NA Affymetrix, Illumina [21130] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90078447 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Wears glasses or contact lenses (UKB data field 2207) (Gene-based burden) 386,786 European ancestry cases, 43,548 European ancestry controls NA Illumina [185933] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90082846 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gestational diabetes only (UKB data field 4041) 845 European ancestry cases, 7,001 European ancestry controls NA Affymetrix, Illumina [20507] 0 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST90079142 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight (UKB data field 21002) (Gene-based burden) 429,785 European ancestry individuals NA Illumina [185930] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082671 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever addicted to alcohol (UKB data field 20406) 3,191 European ancestry cases, 4,505 European ancestry controls NA Affymetrix, Illumina [20169] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90078405 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight (UKB data field 23098) (Gene-based burden) 423,702 European ancestry individuals NA Illumina [185869] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082888 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General pain for three months (UKB data field 2956) 5,909 European ancestry cases, 1,218 European ancestry controls NA Affymetrix, Illumina [19082] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90078975 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change compared with 1 year ago - No, weigh about the same (UKB data field 2306) (Gene-based burden) 249,402 European ancestry cases, 174,786 European ancestry controls NA Illumina [185837] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082882 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unusual or psychotic experiences in past year - Not at all (UKB data field 20467) 4,948 European ancestry cases, 1,913 European ancestry controls NA Affymetrix, Illumina [18473] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078504 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change compared with 1 year ago - gained weight (UKB data field 2306) (Gene-based burden) 126,122 European ancestry cases, 298,066 European ancestry controls NA Illumina [185837] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082883 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unusual or psychotic experiences in past year - Once or twice (UKB data field 20467) 1,216 European ancestry cases, 5,645 European ancestry controls NA Affymetrix, Illumina [18473] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078505 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change compared with 1 year ago - lost weight (UKB data field 2306) (Gene-based burden) 73,207 European ancestry cases, 350,981 European ancestry controls NA Illumina [185837] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082884 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever talked to a health professional about unusual or psychotic experiences (UKB data field 20477) 1,463 European ancestry cases, 5,384 European ancestry controls NA Affymetrix, Illumina [18438] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078509 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. HHV 6B seropositivity for Human Herpesvirus 6 (UKB data field 23057) 6,755 European ancestry cases, 1,786 European ancestry controls NA Affymetrix, Illumina [21784] 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90078892 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Multivitamins minerals (UKB data field 6155) (Gene-based burden) 97,313 European ancestry cases, 45,512 European ancestry controls NA Illumina [173046] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90083457 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Herpes Simplex virus 1 (UKB data field 23050) 5,907 European ancestry cases, 2,634 European ancestry controls NA Affymetrix, Illumina [21784] 0 herpes virus seropositivity http://www.ebi.ac.uk/efo/EFO_0007036 GCST90078886 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin A (UKB data field 6155) (Gene-based burden) 8,781 European ancestry cases, 134,044 European ancestry controls NA Illumina [173046] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90083451 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Herpes Simplex virus 2 (UKB data field 23051) 1,331 European ancestry cases, 7,210 European ancestry controls NA Affymetrix, Illumina [21784] 0 herpes virus seropositivity http://www.ebi.ac.uk/efo/EFO_0007036 GCST90078887 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin B (UKB data field 6155) (Gene-based burden) 19,958 European ancestry cases, 122,867 European ancestry controls NA Illumina [173046] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90083452 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Human Polyomavirus JCV (UKB data field 23066) 4,863 European ancestry cases, 3,678 European ancestry controls NA Affymetrix, Illumina [21784] 0 polyomavirus 2 seropositivity http://www.ebi.ac.uk/efo/EFO_0010907 GCST90078894 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin C (UKB data field 6155) (Gene-based burden) 39,394 European ancestry cases, 103,431 European ancestry controls NA Illumina [173046] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90083453 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Merkel Cell Polyomavirus (UKB data field 23067) 5,638 European ancestry cases, 2,903 European ancestry controls NA Affymetrix, Illumina [21784] 0 merkel cell virus seropositivity http://www.ebi.ac.uk/efo/EFO_0010906 GCST90078895 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin D (UKB data field 6155) (Gene-based burden) 22,734 European ancestry cases, 120,091 European ancestry controls NA Illumina [173046] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90083454 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Toxoplasma gondii (UKB data field 23062) 2,347 European ancestry cases, 6,194 European ancestry controls NA Affymetrix, Illumina [21784] 0 Toxoplasma gondii seropositivity http://www.ebi.ac.uk/efo/EFO_0007047 GCST90078893 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin and mineral supplements use - Vitamin E (UKB data field 6155) (Gene-based burden) 13,167 European ancestry cases, 129,658 European ancestry controls NA Illumina [173046] 0 vitamin supplement exposure measurement http://www.ebi.ac.uk/efo/EFO_0009116 GCST90083455 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Varicella Zoster Virus (UKB data field 23052) 7,901 European ancestry cases, 640 European ancestry controls NA Affymetrix, Illumina [21784] 0 Varicella zoster virus seropositivity http://www.ebi.ac.uk/efo/EFO_0009340 GCST90078888 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin D levels (UKB data field 30890) (Gene-based burden) 394,382 European ancestry individuals NA Illumina [185419] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90083033 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 45 (UKB data field 5790) 3,466 European ancestry cases, 4,946 European ancestry controls NA Affymetrix, Illumina [21620] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079381 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vomiting when IBS symptoms first began (UKB data field 21076) (Gene-based burden) 1,251 European ancestry cases, 17,399 European ancestry controls NA Illumina [103530] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90082825 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 48 (UKB data field 5790) 895 European ancestry cases, 7,517 European ancestry controls NA Affymetrix, Illumina [21620] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079382 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism - composite (Gene-based burden) 5,702 European ancestry cases, 220,211 European ancestry controls NA Illumina [180656] 0 venous thromboembolism, deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0003907 GCST90085520 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 49 (UKB data field 5790) 1,344 European ancestry cases, 7,068 European ancestry controls NA Affymetrix, Illumina [21620] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079383 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism / Deep vein thrombosis (Gene-based burden) 591 European ancestry cases, 220,210 European ancestry controls NA Illumina [180346] 0 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90085521 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 50 (UKB data field 5790) 2,051 European ancestry cases, 6,361 European ancestry controls NA Affymetrix, Illumina [21620] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079384 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism / Pulmonary embolism (Gene-based burden) 5,226 European ancestry cases, 371,230 European ancestry controls NA Illumina [185160] 0 venous thromboembolism, pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0003827 GCST90085522 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Facial pains for three months (UKB data field 4067) 4,032 European ancestry cases, 4,388 European ancestry controls NA Affymetrix, Illumina [21594] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90079144 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Varicella Zoster Virus (UKB data field 23052) (Gene-based burden) 7,901 European ancestry cases, 640 European ancestry controls NA Illumina [70714] 0 Varicella zoster virus seropositivity http://www.ebi.ac.uk/efo/EFO_0009340 GCST90082874 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pioglitazone (Gene-based burden) 917 European ancestry cases, 319,841 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082189 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - seretide 50 evohaler (Gene-based burden) 5,267 European ancestry cases, 315,491 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082195 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Squamous cell carcinoma (UKB data field 20001) 638 European ancestry cases, 38,976 European ancestry controls NA Affymetrix, Illumina [80688] 0 squamous cell carcinoma http://www.ebi.ac.uk/efo/EFO_0000707 GCST90077641 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - serevent inhaler (Gene-based burden) 1,172 European ancestry cases, 319,586 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081999 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Uterine endometrial cancer (UKB data field 20001) 1,131 European ancestry cases, 38,483 European ancestry controls NA Affymetrix, Illumina [80688] 0 uterine carcinoma http://www.ebi.ac.uk/efo/EFO_0002919 GCST90077633 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - seroxat (Gene-based burden) 589 European ancestry cases, 320,169 European ancestry controls NA Illumina [166537] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082088 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Breast cancer (UKB data field 20001) 10,070 European ancestry cases, 29,544 European ancestry controls NA Affymetrix, Illumina [80687] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90077626 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sertraline (Gene-based burden) 2,205 European ancestry cases, 318,553 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082027 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prostate cancer (UKB data field 20001) 3,622 European ancestry cases, 35,992 European ancestry controls NA Affymetrix, Illumina [80686] 1 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90077635 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - See own GP (UKB data field 20554) 1,446 European ancestry cases, 2,334 European ancestry controls NA Affymetrix, Illumina [12352] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90078669 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia - both eyes (UKB data field 5843) (Gene-based burden) 45,679 European ancestry cases, 5,456 European ancestry controls NA Illumina [144752] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90083376 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - Use a helpline voluntary organization (UKB data field 20554) 588 European ancestry cases, 3,192 European ancestry controls NA Affymetrix, Illumina [12352] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90078668 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia - left eye (UKB data field 5843) (Gene-based burden) 2,871 European ancestry cases, 48,264 European ancestry controls NA Illumina [144752] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90083375 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition - both eyes (UKB data field 5934) 1,274 European ancestry cases, 1,935 European ancestry controls NA Affymetrix, Illumina [11189] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079402 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia - right eye (UKB data field 5843) (Gene-based burden) 3,062 European ancestry cases, 48,073 European ancestry controls NA Illumina [144752] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90083374 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition - left eye (UKB data field 5934) 942 European ancestry cases, 2,267 European ancestry controls NA Affymetrix, Illumina [11189] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079401 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other eye condition - both eyes (UKB data field 5877) (Gene-based burden) 1,450 European ancestry cases, 723 European ancestry controls NA Illumina [26077] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083383 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition - right eye (UKB data field 5934) 1,019 European ancestry cases, 2,190 European ancestry controls NA Affymetrix, Illumina [11189] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079400 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Presbyopia - both eyes (UKB data field 5610) (Gene-based burden) 49,647 European ancestry cases, 5,658 European ancestry controls NA Illumina [146713] 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90083352 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI13 subset inclusion logic - False (UKB data field 5866) 1,119 European ancestry cases, 2,084 European ancestry controls NA Affymetrix, Illumina [11184] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079394 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Presbyopia - left eye (UKB data field 5610) (Gene-based burden) 3,048 European ancestry cases, 52,257 European ancestry controls NA Illumina [146713] 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90083351 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI13 subset inclusion logic - Neither true nor false (UKB data field 5866) 868 European ancestry cases, 2,335 European ancestry controls NA Affymetrix, Illumina [11184] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079396 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Presbyopia - right eye (UKB data field 5610) (Gene-based burden) 3,113 European ancestry cases, 52,192 European ancestry controls NA Illumina [146713] 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90083350 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI13 subset inclusion logic (UKB data field 5866) 1,283 European ancestry cases, 1,920 European ancestry controls NA Affymetrix, Illumina [11184] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079395 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. White blood cell leukocyte count (UKB data field 30000) (Gene-based burden) 419,188 European ancestry individuals NA Illumina [185803] 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90082964 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ongoing addiction to alcohol (UKB data field 20415) 1,387 European ancestry cases, 1,755 European ancestry controls NA Affymetrix, Illumina [10985] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90078431 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whole body fat free mass (UKB data field 23101) (Gene-based burden) 423,664 European ancestry individuals NA Illumina [185868] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90082891 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever physically dependent on alcohol (UKB data field 20404) 840 European ancestry cases, 2,203 European ancestry controls NA Affymetrix, Illumina [10768] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90078402 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whole body fat mass (UKB data field 23100) (Gene-based burden) 423,023 European ancestry individuals NA Illumina [185858] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90082890 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glaucoma - both eyes (UKB data field 6119) 2,128 European ancestry cases, 702 European ancestry controls NA Affymetrix, Illumina [10447] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90079429 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whole body water mass (UKB data field 23102) (Gene-based burden) 423,698 European ancestry individuals NA Illumina [185869] 0 whole body water mass http://www.ebi.ac.uk/efo/EFO_0009805 GCST90082892 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Strabismus squint - left eye (UKB data field 6205) 1,396 European ancestry cases, 1,270 European ancestry controls NA Affymetrix, Illumina [9963] 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90079490 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Extremely happy (UKB data field 4537) (Gene-based burden) 11,089 European ancestry cases, 165,801 European ancestry controls NA Illumina [177087] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90083167 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Strabismus squint - right eye (UKB data field 6205) 897 European ancestry cases, 1,769 European ancestry controls NA Affymetrix, Illumina [9963] 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90079489 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Extremely unhappy (UKB data field 4537) (Gene-based burden) 1,039 European ancestry cases, 175,851 European ancestry controls NA Illumina [177087] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90083172 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Previously smoked cigarettes on most/all days (UKB data field 5959) 1,607 European ancestry cases, 779 European ancestry controls NA Affymetrix, Illumina [9301] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90079403 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - I am not employed (UKB data field 4537) (Gene-based burden) 63,199 European ancestry cases, 113,691 European ancestry controls NA Illumina [177087] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90083173 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other eye condition - both eyes (UKB data field 5877) 1,450 European ancestry cases, 723 European ancestry controls NA Affymetrix, Illumina [8812] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079397 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Moderately happy (UKB data field 4537) (Gene-based burden) 55,486 European ancestry cases, 121,404 European ancestry controls NA Illumina [177087] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90083169 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Macular degeneration - both eyes (UKB data field 5912) 1,165 European ancestry cases, 913 European ancestry controls NA Affymetrix, Illumina [8457] 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90079399 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Moderately unhappy (UKB data field 4537) (Gene-based burden) 8,984 European ancestry cases, 167,906 European ancestry controls NA Illumina [177087] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90083170 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Macular degeneration - right eye (UKB data field 5912) 504 European ancestry cases, 1,574 European ancestry controls NA Affymetrix, Illumina [8457] 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90079398 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Very happy (UKB data field 4537) (Gene-based burden) 46,094 European ancestry cases, 130,796 European ancestry controls NA Illumina [177087] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90083168 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ongoing behavioural or miscellanous addiction (UKB data field 20432) 916 European ancestry cases, 1,005 European ancestry controls NA Affymetrix, Illumina [8241] 0 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90078448 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Work job satisfaction - Very unhappy (UKB data field 4537) (Gene-based burden) 2,223 European ancestry cases, 174,667 European ancestry controls NA Illumina [177087] 0 job satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009723 GCST90083171 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar disorder status - Bipolar Type I Mania (UKB data field 20122) 673 European ancestry cases, 623 European ancestry controls NA Affymetrix, Illumina [6574] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90078306 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Worried most days during period of worst anxiety (UKB data field 20538) (Gene-based burden) 36,918 European ancestry cases, 4,895 European ancestry controls NA Illumina [136566] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082612 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar disorder status - Bipolar Type II Hypomania (UKB data field 20122) 623 European ancestry cases, 673 European ancestry controls NA Affymetrix, Illumina [6574] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90078307 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Worrier / anxious feelings (UKB data field 1980) (Gene-based burden) 242,417 European ancestry cases, 178,089 European ancestry controls NA Illumina [185804] 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90081610 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substance of prescription or over the counter medication addiction - A sedative benzodiazepine or sleeping tablet (UKB data field 20551) 526 European ancestry cases, 631 European ancestry controls NA Affymetrix, Illumina [6110] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078665 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Worry too long after embarrassment (UKB data field 2000) (Gene-based burden) 203,159 European ancestry cases, 211,521 European ancestry controls NA Illumina [185699] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082229 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sildenafil (Gene-based burden) 914 European ancestry cases, 319,844 European ancestry controls NA Illumina [183957] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082188 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Testicular cancer (UKB data field 20001) 769 European ancestry cases, 38,845 European ancestry controls NA Affymetrix, Illumina [80685] 0 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST90077636 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - simvador (Gene-based burden) 595 European ancestry cases, 320,163 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082208 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tense, sore or aching muscles during worst period of anxiety (UKB data field 20417) 15,553 European ancestry cases, 23,994 European ancestry controls NA Affymetrix, Illumina [80585] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90078437 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - simvastatin (Gene-based burden) 51,781 European ancestry cases, 268,977 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081995 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when walking uphill or hurrying (UKB data field 5474) 26,456 European ancestry cases, 12,452 European ancestry controls NA Affymetrix, Illumina [80218] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079352 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - solifenacin (Gene-based burden) 833 European ancestry cases, 319,925 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082218 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stomach abdominal pain for three months (UKB data field 3741) 21,293 European ancestry cases, 16,808 European ancestry controls NA Affymetrix, Illumina [78347] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90079070 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sotalol (Gene-based burden) 675 European ancestry cases, 320,083 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082085 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract (UKB data field 6148) 18,309 European ancestry cases, 19,489 European ancestry controls NA Affymetrix, Illumina [77634] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079433 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - spiriva (Gene-based burden) 672 European ancestry cases, 320,086 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082205 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetes related eye disease (UKB data field 6148) 3,093 European ancestry cases, 34,705 European ancestry controls NA Affymetrix, Illumina [77634] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90079430 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - spironolactone (Gene-based burden) 859 European ancestry cases, 319,899 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082024 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glaucoma (UKB data field 6148) 6,848 European ancestry cases, 30,950 European ancestry controls NA Affymetrix, Illumina [77634] 1 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90079431 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - st johns wort/hypericum (Gene-based burden) 773 European ancestry cases, 319,985 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082225 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Injury loss of vision (UKB data field 6148) 2,794 European ancestry cases, 35,004 European ancestry controls NA Affymetrix, Illumina [77634] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90079432 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - starflower oil (Gene-based burden) 668 European ancestry cases, 320,090 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082129 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Macular degeneration (UKB data field 6148) 4,185 European ancestry cases, 33,613 European ancestry controls 2,171 European ancestry cases, 10,323 European ancestry controls Affymetrix, Illumina [77634] 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90079434 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sulfasalazine (Gene-based burden) 862 European ancestry cases, 319,896 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082121 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition (UKB data field 6148) 8,734 European ancestry cases, 29,064 European ancestry controls NA Affymetrix, Illumina [77634] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079435 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - sumatriptan (Gene-based burden) 1,299 European ancestry cases, 319,459 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082100 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 1 (UKB data field 21039) 2,871 European ancestry cases, 33,070 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078755 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - symbicort turbohaler (Gene-based burden) 2,812 European ancestry cases, 317,946 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082192 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 2 (UKB data field 21039) 5,695 European ancestry cases, 30,246 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078756 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tadalafil (Gene-based burden) 574 European ancestry cases, 320,184 European ancestry controls NA Illumina [183951] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082207 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 47 (UKB data field 20187) 561 European ancestry cases, 5,267 European ancestry controls NA Affymetrix, Illumina [16600] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078370 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition - both eyes (UKB data field 5934) (Gene-based burden) 1,274 European ancestry cases, 1,935 European ancestry controls NA Illumina [36523] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083388 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 49 (UKB data field 20187) 981 European ancestry cases, 4,847 European ancestry controls NA Affymetrix, Illumina [16600] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078369 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition - left eye (UKB data field 5934) (Gene-based burden) 942 European ancestry cases, 2,267 European ancestry controls NA Illumina [36523] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083387 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 50 (UKB data field 20187) 1,353 European ancestry cases, 4,475 European ancestry controls NA Affymetrix, Illumina [16600] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078368 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition - right eye (UKB data field 5934) (Gene-based burden) 1,019 European ancestry cases, 2,190 European ancestry controls NA Illumina [36523] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083386 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amblyopia - left eye (UKB data field 5408) 2,930 European ancestry cases, 2,167 European ancestry controls NA Affymetrix, Illumina [15194] 0 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST90079346 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Strabismus squint - left eye (UKB data field 6205) (Gene-based burden) 1,396 European ancestry cases, 1,270 European ancestry controls NA Illumina [31288] 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90083476 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amblyopia - right eye (UKB data field 5408) 1,965 European ancestry cases, 3,132 European ancestry controls NA Affymetrix, Illumina [15194] 0 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST90079345 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Strabismus squint - right eye (UKB data field 6205) (Gene-based burden) 897 European ancestry cases, 1,769 European ancestry controls NA Illumina [31288] 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90083475 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adopted mother still alive (UKB data field 3942) 1,313 European ancestry cases, 3,386 European ancestry controls NA Affymetrix, Illumina [14250] 0 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST90079076 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Farsightedness - both eyes (UKB data field 5832) (Gene-based burden) 23,800 European ancestry cases, 3,778 European ancestry controls NA Illumina [120084] 0 hyperopia http://purl.obolibrary.org/obo/MONDO_0004891 GCST90083373 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Adopted father still alive (UKB data field 3912) 690 European ancestry cases, 3,711 European ancestry controls NA Affymetrix, Illumina [13649] 0 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST90079075 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Farsightedness - left eye (UKB data field 5832) (Gene-based burden) 1,912 European ancestry cases, 25,666 European ancestry controls NA Illumina [120084] 0 hyperopia http://purl.obolibrary.org/obo/MONDO_0004891 GCST90083372 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Helicobacter pylori - definition 1 (UKB data field 23073) 1,472 European ancestry cases, 2,832 European ancestry controls NA Affymetrix, Illumina [13357] 0 Helicobacter pylori seropositivity http://www.ebi.ac.uk/efo/EFO_0009341 GCST90078900 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Farsightedness - right eye (UKB data field 5832) (Gene-based burden) 2,102 European ancestry cases, 25,476 European ancestry controls NA Illumina [120084] 0 hyperopia http://purl.obolibrary.org/obo/MONDO_0004891 GCST90083371 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - Need hospital treatment e.g. A&E (UKB data field 20554) 2,509 European ancestry cases, 1,271 European ancestry controls NA Affymetrix, Illumina [12352] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90078667 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glaucoma - both eyes (UKB data field 6119) (Gene-based burden) 2,128 European ancestry cases, 702 European ancestry controls NA Illumina [33134] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90083415 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - Receive help from friends family neighbours (UKB data field 20554) 1,737 European ancestry cases, 2,043 European ancestry controls NA Affymetrix, Illumina [12352] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90078670 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Macular degeneration - both eyes (UKB data field 5912) (Gene-based burden) 1,165 European ancestry cases, 913 European ancestry controls NA Illumina [24725] 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90083385 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Actions taken following self harm - See anyone from psychiatric or mental health services including liaison services (UKB data field 20554) 2,002 European ancestry cases, 1,778 European ancestry controls NA Affymetrix, Illumina [12352] 0 suicide behaviour measurement http://www.ebi.ac.uk/efo/EFO_0006882 GCST90078666 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Macular degeneration - right eye (UKB data field 5912) (Gene-based burden) 504 European ancestry cases, 1,574 European ancestry controls NA Illumina [24725] 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90083384 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Surgery on leg arteries other than for varicose veins (UKB data field 5529) 1,424 European ancestry cases, 38,914 European ancestry controls NA Affymetrix, Illumina [82832] 0 surgery on leg artery http://www.ebi.ac.uk/efo/EFO_0009729 GCST90079360 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pregabalin (Gene-based burden) 1,076 European ancestry cases, 319,682 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082217 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for depression - Drugs or alcohol more than once (UKB data field 20546) 10,129 European ancestry cases, 30,541 European ancestry controls NA Affymetrix, Illumina [82545] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078649 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Both gained and lost some weight during the episode (UKB data field 20536) (Gene-based burden) 4,299 European ancestry cases, 62,954 European ancestry controls NA Illumina [153099] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082607 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever prescribed a medication for unusual or psychotic experiences (UKB data field 20466) 768 European ancestry cases, 6,064 European ancestry controls NA Affymetrix, Illumina [18426] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078503 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Gained weight (UKB data field 20536) (Gene-based burden) 11,709 European ancestry cases, 55,544 European ancestry controls NA Illumina [153099] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082605 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - A bit distressing (UKB data field 20462) 1,214 European ancestry cases, 5,497 European ancestry controls NA Affymetrix, Illumina [18146] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078499 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Lost weight (UKB data field 20536) (Gene-based burden) 24,070 European ancestry cases, 43,183 European ancestry controls NA Illumina [153099] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082606 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Not distressing a neutral experience (UKB data field 20462) 2,103 European ancestry cases, 4,608 European ancestry controls NA Affymetrix, Illumina [18146] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078498 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Stayed about the same or was on a diet (UKB data field 20536) (Gene-based burden) 27,175 European ancestry cases, 40,078 European ancestry controls NA Illumina [153099] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90082604 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Not distressing at all it was a positive experience (UKB data field 20462) 1,955 European ancestry cases, 4,756 European ancestry controls NA Affymetrix, Illumina [18146] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078497 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Wheeze or whistling in the chest in last year (UKB data field 2316) (Gene-based burden) 92,570 European ancestry cases, 330,651 European ancestry controls NA Illumina [185825] 0 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90082920 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Quite distressing (UKB data field 20462) 636 European ancestry cases, 6,075 European ancestry controls NA Affymetrix, Illumina [18146] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078500 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism - both eyes (UKB data field 5855) (Gene-based burden) 12,485 European ancestry cases, 5,160 European ancestry controls NA Illumina [102619] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90083379 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Very distressing (UKB data field 20462) 803 European ancestry cases, 5,908 European ancestry controls NA Affymetrix, Illumina [18146] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078501 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism - left eye (UKB data field 5855) (Gene-based burden) 2,864 European ancestry cases, 14,781 European ancestry controls NA Illumina [102619] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90083378 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Self harmed in past year (UKB data field 20481) 523 European ancestry cases, 5,507 European ancestry controls NA Affymetrix, Illumina [16944] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90078513 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism - right eye (UKB data field 5855) (Gene-based burden) 2,590 European ancestry cases, 15,055 European ancestry controls NA Illumina [102619] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90083377 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of times self harmed - 1 (UKB data field 20482) 2,892 European ancestry cases, 3,047 European ancestry controls NA Affymetrix, Illumina [16757] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90078514 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amblyopia - left eye (UKB data field 5408) (Gene-based burden) 2,930 European ancestry cases, 2,167 European ancestry controls NA Illumina [51633] 0 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST90083332 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of times self harmed - 2 (UKB data field 20482) 1,083 European ancestry cases, 4,856 European ancestry controls NA Affymetrix, Illumina [16757] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90078515 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Amblyopia - right eye (UKB data field 5408) (Gene-based burden) 1,965 European ancestry cases, 3,132 European ancestry controls NA Illumina [51633] 0 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST90083331 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Number of times self harmed - 3 or more (UKB data field 20482) 1,964 European ancestry cases, 3,975 European ancestry controls NA Affymetrix, Illumina [16757] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90078516 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract - both eyes (UKB data field 5441) (Gene-based burden) 6,814 European ancestry cases, 3,778 European ancestry controls NA Illumina [79582] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083335 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever attempted suicide (UKB data field 20483) 3,119 European ancestry cases, 2,743 European ancestry controls NA Affymetrix, Illumina [16615] 0 attempted suicide http://www.ebi.ac.uk/efo/EFO_0004321 GCST90078517 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract - left eye (UKB data field 5441) (Gene-based burden) 1,817 European ancestry cases, 8,775 European ancestry controls NA Illumina [79582] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083334 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 45 (UKB data field 20187) 2,481 European ancestry cases, 3,347 European ancestry controls NA Affymetrix, Illumina [16600] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078371 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract - right eye (UKB data field 5441) (Gene-based burden) 2,144 European ancestry cases, 8,448 European ancestry controls NA Illumina [79582] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083333 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - premarin (Gene-based burden) 1,836 European ancestry cases, 318,922 European ancestry controls NA Illumina [183963] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082031 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for depression - Medication prescribed to you for at least two weeks (UKB data field 20546) 33,619 European ancestry cases, 7,051 European ancestry controls NA Affymetrix, Illumina [82545] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078648 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - premique (Gene-based burden) 866 European ancestry cases, 319,892 European ancestry controls NA Illumina [183931] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082144 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Substances taken for depression - Unprescribed medication more than once (UKB data field 20546) 4,881 European ancestry cases, 35,789 European ancestry controls NA Affymetrix, Illumina [82545] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078647 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prempak (Gene-based burden) 647 European ancestry cases, 320,111 European ancestry controls NA Illumina [183956] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081983 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Easily tired during worst period of anxiety (UKB data field 20429) 29,114 European ancestry cases, 11,403 European ancestry controls NA Affymetrix, Illumina [82327] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90078446 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prochlorperazine (Gene-based burden) 621 European ancestry cases, 320,137 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082029 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - action taken - Continue at same pace (UKB data field 5507) 13,792 European ancestry cases, 26,027 European ancestry controls NA Affymetrix, Illumina [81930] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079357 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - propranolol (Gene-based burden) 3,052 European ancestry cases, 317,706 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082084 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - action taken - Slow down (UKB data field 5507) 20,708 European ancestry cases, 19,111 European ancestry controls NA Affymetrix, Illumina [81930] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079356 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - prozac (Gene-based burden) 597 European ancestry cases, 320,161 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082026 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - action taken - Stop (UKB data field 5507) 6,007 European ancestry cases, 33,812 European ancestry controls NA Affymetrix, Illumina [81930] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079355 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - pulmicort ls inhaler (Gene-based burden) 675 European ancestry cases, 320,083 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082004 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain in calf/calves (UKB data field 5463) 12,782 European ancestry cases, 27,015 European ancestry controls NA Affymetrix, Illumina [81858] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079351 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - quinine (Gene-based burden) 3,027 European ancestry cases, 317,731 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082057 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Restless during period of worst anxiety (UKB data field 20426) 24,179 European ancestry cases, 16,027 European ancestry controls NA Affymetrix, Illumina [81824] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90078443 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - qvar 50 inhaler (Gene-based burden) 1,741 European ancestry cases, 319,017 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082182 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when walking normally (UKB data field 5485) 22,256 European ancestry cases, 17,177 European ancestry controls NA Affymetrix, Illumina [81168] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079353 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rabeprazole sodium (Gene-based burden) 792 European ancestry cases, 319,966 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082186 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. More irritable than usual during worst period of anxiety (UKB data field 20422) 28,540 European ancestry cases, 11,134 European ancestry controls NA Affymetrix, Illumina [80751] 0 irritability measurement http://www.ebi.ac.uk/efo/EFO_0009594 GCST90078440 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ramipril (Gene-based burden) 21,735 European ancestry cases, 299,023 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081985 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain when standing still or sitting (UKB data field 5452) 24,490 European ancestry cases, 14,717 European ancestry controls NA Affymetrix, Illumina [80748] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079350 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ranitidine (Gene-based burden) 7,746 European ancestry cases, 313,012 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082069 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cancer (UKB data field 20001) 613 European ancestry cases, 39,001 European ancestry controls NA Affymetrix, Illumina [80688] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90077644 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - rino clenil nasal spray (Gene-based burden) 901 European ancestry cases, 319,857 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082214 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.6: Presence of orthopedic joint implants 14,119 European ancestry cases, 373,799 European ancestry controls NA Affymetrix, Illumina [510681] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081428 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Very unhappy (UKB data field 4548) (Gene-based burden) 4,566 European ancestry cases, 172,508 European ancestry controls NA Illumina [177120] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90083178 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C85.9: Non-Hodgkin lymphoma, unspecified 1,233 European ancestry cases, 386,688 European ancestry controls NA Affymetrix, Illumina [510680] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90079637 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing aid user (UKB data field 3393) (Gene-based burden) 15,741 European ancestry cases, 266,238 European ancestry controls NA Illumina [182878] 0 able to hear with hearing aids http://www.ebi.ac.uk/efo/EFO_0009720 GCST90083039 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J96.9: Respiratory failure, unspecified 2,652 European ancestry cases, 385,269 European ancestry controls NA Affymetrix, Illumina [510680] 0 respiratory failure http://www.ebi.ac.uk/efo/EFO_0009686 GCST90080156 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing difficulty problems (UKB data field 2247) (Gene-based burden) 114,857 European ancestry cases, 300,307 European ancestry controls NA Illumina [185729] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90082857 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.2: Diverticulitis of large intestine with perforation and abscess 623 European ancestry cases, 387,299 European ancestry controls NA Affymetrix, Illumina [510680] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080246 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing difficulty problems background noise (UKB data field 2257) (Gene-based burden) 167,296 European ancestry cases, 255,576 European ancestry controls NA Illumina [185818] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90082864 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10.9: Gout, unspecified 4,531 European ancestry cases, 383,393 European ancestry controls NA Affymetrix, Illumina [510680] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90080395 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing loss (Gene-based burden) 98,675 European ancestry cases, 196,355 European ancestry controls NA Illumina [183168] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90085525 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M89.9: Disorder of bone, unspecified 942 European ancestry cases, 386,978 European ancestry controls NA Affymetrix, Illumina [510680] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90080566 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing loss noise exposure strict (Gene-based burden) 16,069 European ancestry cases, 13,961 European ancestry controls NA Illumina [122728] 0 noise-induced hearing loss http://www.ebi.ac.uk/efo/EFO_1001254 GCST90085526 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K91.8: Other intraoperative and postprocedural complications and disorders of digestive system 962 European ancestry cases, 386,959 European ancestry controls NA Affymetrix, Illumina [510679] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080317 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density (UKB data field 3148) (Gene-based burden) 246,206 European ancestry individuals NA Illumina [181002] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90083038 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.1: Hallux valgus (acquired) 7,729 European ancestry cases, 380,193 European ancestry controls NA Affymetrix, Illumina [510679] 0 Hallux valgus http://purl.obolibrary.org/obo/HP_0001822 GCST90080428 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density left (UKB data field 4105) (Gene-based burden) 166,186 European ancestry individuals NA Illumina [176178] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90083138 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30.9: Cystitis, unspecified 1,711 European ancestry cases, 386,207 European ancestry controls NA Affymetrix, Illumina [510679] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90080598 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density right (UKB data field 4124) (Gene-based burden) 166,266 European ancestry individuals NA Illumina [176159] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90083144 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.5: Presence of coronary angioplasty implant and graft 7,744 European ancestry cases, 380,175 European ancestry controls NA Affymetrix, Illumina [510679] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081423 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density T score automated (UKB data field 78) (Gene-based burden) 246,319 European ancestry individuals NA Illumina [181011] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90083488 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D61.9: Aplastic anemia, unspecified 572 European ancestry cases, 387,353 European ancestry controls NA Affymetrix, Illumina [510678] 0 Aplastic anemia http://purl.obolibrary.org/obo/HP_0001915 GCST90079707 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density T score automated left (UKB data field 4106) (Gene-based burden) 166,283 European ancestry individuals NA Illumina [176191] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90083139 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J43.9: Emphysema, unspecified 2,379 European ancestry cases, 385,541 European ancestry controls NA Affymetrix, Illumina [510678] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90080127 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel bone mineral density T score automated right (UKB data field 4125) (Gene-based burden) 166,358 European ancestry individuals NA Illumina [176168] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90083145 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G99: Other disorders of nervous system in diseases classified elsewhere 1,401 European ancestry cases, 386,517 European ancestry controls NA Affymetrix, Illumina [510677] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90079861 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bring up phlegm sputum mucus on most days (UKB data field 22504) (Gene-based burden) 9,287 European ancestry cases, 98,962 European ancestry controls NA Illumina [166035] 0 bringing up phlegm, sputum or mucus on most days, self-reported http://www.ebi.ac.uk/efo/EFO_0009824 GCST90082859 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean corpuscular haemoglobin concentration (UKB data field 30060) 419,186 European ancestry individuals NA Affymetrix, Illumina [538536] 5 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90078985 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. C reactive protein levels (UKB data field 30710) (Gene-based burden) 411,229 European ancestry individuals NA Illumina [185650] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90083012 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. White blood cell leukocyte count (UKB data field 30000) 419,188 European ancestry individuals 115,482 European ancestry individuals Affymetrix, Illumina [538532] 4 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90078978 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08.7: Follow-up examination after combined treatment for malignant neoplasm 1,255 European ancestry cases, 386,675 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081198 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 502 Often (UKB data field 21028) (Gene-based burden) 9,192 European ancestry cases, 73,909 European ancestry controls NA Illumina [159594] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082685 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08.9: Follow-up examination after unspecified treatment for malignant neoplasm 985 European ancestry cases, 386,945 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081199 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R57: Shock, not elsewhere classified 541 European ancestry cases, 387,377 European ancestry controls NA Affymetrix, Illumina [510676] 0 Shock http://purl.obolibrary.org/obo/HP_0031273 GCST90080884 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High light scatter reticulocyte percentage (UKB data field 30290) (Gene-based burden) 412,334 European ancestry individuals NA Illumina [185680] 0 reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0010700 GCST90082991 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S06.5: Traumatic subdural hemorrhage 540 European ancestry cases, 387,371 European ancestry controls NA Affymetrix, Illumina [510676] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080951 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hip circumference (UKB data field 49) (Gene-based burden) 430,214 European ancestry individuals NA Illumina [185937] 0 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90083239 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83: Surgical operation and other surgical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 22,401 European ancestry cases, 365,517 European ancestry controls NA Affymetrix, Illumina [510676] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081165 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hip pain for three months (UKB data field 3414) (Gene-based burden) 40,643 European ancestry cases, 11,498 European ancestry controls NA Illumina [144514] 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90083041 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.5: Acquired absence of kidney 1,507 European ancestry cases, 386,407 European ancestry controls NA Affymetrix, Illumina [510676] 0 organ extraction http://www.ebi.ac.uk/efo/EFO_0009124 GCST90081393 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Herpes Simplex virus 1 (UKB data field 23050) (Gene-based burden) 5,907 European ancestry cases, 2,634 European ancestry controls NA Illumina [70714] 0 herpes virus seropositivity http://www.ebi.ac.uk/efo/EFO_0007036 GCST90082872 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L27.0: Generalized skin eruption due to drugs and medicaments taken internally 514 European ancestry cases, 387,400 European ancestry controls NA Affymetrix, Illumina [510675] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080340 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Herpes Simplex virus 2 (UKB data field 23051) (Gene-based burden) 1,331 European ancestry cases, 7,210 European ancestry controls NA Illumina [70714] 0 herpes virus seropositivity http://www.ebi.ac.uk/efo/EFO_0007036 GCST90082873 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y95: Nosocomial condition 2,043 European ancestry cases, 385,876 European ancestry controls NA Affymetrix, Illumina [510675] 0 nosocomial infection http://purl.obolibrary.org/obo/MONDO_0043544 GCST90081177 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hypertension nephropathy (no type 2 diabetes) (Gene-based burden) 3,668 European ancestry cases, 328,410 European ancestry controls NA Illumina [184231] 0 Nephropathy http://purl.obolibrary.org/obo/HP_0000112 GCST90085472 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D73: Diseases of spleen 692 European ancestry cases, 387,204 European ancestry controls 290 European ancestry cases, 114,699 European ancestry controls Affymetrix, Illumina [510674] 0 splenic disease http://www.ebi.ac.uk/efo/EFO_0009002 GCST90079718 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inflammatory bowel disease (Gene-based burden) 5,650 European ancestry cases, 298,738 European ancestry controls NA Illumina [183558] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90085477 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.1: Atherosclerotic heart disease of native coronary artery 23,129 European ancestry cases, 364,782 European ancestry controls 21,146 European ancestry cases, 96,213 European ancestry controls Affymetrix, Illumina [510674] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90079978 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inflammatory bowel disease - loose composite (Gene-based burden) 5,509 European ancestry cases, 358,527 European ancestry controls NA Illumina [184978] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90085473 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21.0: Gastro-esophageal reflux disease with esophagitis 12,871 European ancestry cases, 375,044 European ancestry controls NA Affymetrix, Illumina [510674] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90080186 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Crohn's disease (Gene-based burden) 2,106 European ancestry cases, 321,797 European ancestry controls NA Illumina [184058] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90085474 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel Broadband ultrasound attenuation direct entry (UKB data field 3144) (Gene-based burden) 246,304 European ancestry individuals NA Illumina [181011] 0 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90083035 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I78.1: Nevus, non-neoplastic 696 European ancestry cases, 387,219 European ancestry controls NA Affymetrix, Illumina [510677] 0 nevus http://www.ebi.ac.uk/efo/EFO_0000625 GCST90080056 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel broadband ultrasound attenuation left (UKB data field 4101) (Gene-based burden) 166,276 European ancestry individuals NA Illumina [176191] 0 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90083135 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.2: Volvulus 828 European ancestry cases, 387,086 European ancestry controls NA Affymetrix, Illumina [510677] 0 Gastrointestinal obstruction http://purl.obolibrary.org/obo/HP_0004796 GCST90080240 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel broadband ultrasound attenuation right (UKB data field 4120) (Gene-based burden) 166,349 European ancestry individuals NA Illumina [176168] 0 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90083141 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20.1: Calculus of ureter 2,766 European ancestry cases, 385,149 European ancestry controls NA Affymetrix, Illumina [510677] 0 ureterolithiasis http://www.ebi.ac.uk/efo/EFO_1001228 GCST90080587 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel quantitative ultrasound index direct entry (UKB data field 3147) (Gene-based burden) 246,319 European ancestry individuals NA Illumina [181011] 0 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90083037 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.3: Personal history of malignant neoplasm of breast 8,566 European ancestry cases, 379,356 European ancestry controls 2,963 European ancestry cases, 33,898 European ancestry controls Affymetrix, Illumina [510677] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90081349 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel quantitative ultrasound index direct entry left (UKB data field 4104) (Gene-based burden) 166,283 European ancestry individuals NA Illumina [176191] 0 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90083137 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I47.1: Supraventricular tachycardia 2,953 European ancestry cases, 384,965 European ancestry controls NA Affymetrix, Illumina [510676] 0 Supraventricular tachycardia http://purl.obolibrary.org/obo/HP_0004755 GCST90080011 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heel quantitative ultrasound index direct entry right (UKB data field 4123) (Gene-based burden) 166,358 European ancestry individuals NA Illumina [176168] 0 bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0004514 GCST90083143 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.4: Other disorders of lung 1,268 European ancestry cases, 386,643 European ancestry controls NA Affymetrix, Illumina [510676] 0 lung disease http://www.ebi.ac.uk/efo/EFO_0003818 GCST90080160 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart Failure (Gene-based burden) 8,159 European ancestry cases, 378,891 European ancestry controls NA Illumina [185336] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90085471 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.7: Barrett's esophagus 3,950 European ancestry cases, 383,962 European ancestry controls NA Affymetrix, Illumina [510676] 0 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90080192 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. HHV 6 overall seropositivity for Human Herpesvirus 6 (UKB data field 23055) (Gene-based burden) 7,769 European ancestry cases, 772 European ancestry controls NA Illumina [70714] 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90082876 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.3: Diverticular disease of large intestine without perforation or abscess 31,734 European ancestry cases, 356,184 European ancestry controls NA Affymetrix, Illumina [510676] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080247 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. HHV 6A seropositivity for Human Herpesvirus 6 (UKB data field 23056) (Gene-based burden) 6,648 European ancestry cases, 1,893 European ancestry controls NA Illumina [70714] 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90082877 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M24.1: Other articular cartilage disorders 1,157 European ancestry cases, 386,756 European ancestry controls NA Affymetrix, Illumina [510676] 0 articular cartilage of joint http://purl.obolibrary.org/obo/UBERON_0010996 GCST90080449 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. HHV 6B seropositivity for Human Herpesvirus 6 (UKB data field 23057) (Gene-based burden) 6,755 European ancestry cases, 1,786 European ancestry controls NA Illumina [70714] 0 human herpesvirus 6 seropositivity http://www.ebi.ac.uk/efo/EFO_0007048 GCST90082878 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30.2: Other chronic cystitis 763 European ancestry cases, 387,152 European ancestry controls NA Affymetrix, Illumina [510676] 0 chronic cystitis http://www.ebi.ac.uk/efo/EFO_1000023 GCST90080596 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High light scatter reticulocyte count (UKB data field 30300) (Gene-based burden) 412,333 European ancestry individuals NA Illumina [185680] 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90082992 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Basophill percentage (UKB data field 30220) (Gene-based burden) 418,454 European ancestry individuals NA Illumina [185795] 0 basophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007992 GCST90082985 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Severe depression (UKB data field 20110) 26,963 European ancestry cases, 396,723 European ancestry controls NA Affymetrix, Illumina [542059] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078271 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Behaviour of cancer tumour - Benign (UKB data field 40012) (Gene-based burden) 1,132 European ancestry cases, 75,236 European ancestry controls NA Illumina [156616] 0 benign http://www.ebi.ac.uk/efo/EFO_0002751 GCST90083124 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk predicted mass (UKB data field 23130) 423,325 European ancestry individuals NA Affymetrix, Illumina [542051] 5 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90078933 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Behaviour of cancer tumour - Carcinoma in situ (UKB data field 40012) (Gene-based burden) 12,102 European ancestry cases, 64,267 European ancestry controls NA Illumina [156617] 0 in situ carcinoma http://purl.obolibrary.org/obo/MONDO_0004647 GCST90083125 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative body size at age 10 - About average (UKB data field 1687) 219,264 European ancestry cases, 204,348 European ancestry controls NA Affymetrix, Illumina [541831] 0 comparative body size at age 10, self-reported http://www.ebi.ac.uk/efo/EFO_0009819 GCST90077590 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Behaviour of cancer tumour - Malignant primary site (UKB data field 40012) (Gene-based burden) 66,204 European ancestry cases, 10,165 European ancestry controls NA Illumina [156617] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90083126 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative body size at age 10 - Plumper (UKB data field 1687) 68,629 European ancestry cases, 354,983 European ancestry controls 53,276 European ancestry cases, 55,571 European ancestry controls Affymetrix, Illumina [541831] 0 comparative body size at age 10, self-reported http://www.ebi.ac.uk/efo/EFO_0009819 GCST90077589 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - A little (UKB data field 20460) (Gene-based burden) 8,105 European ancestry cases, 128,310 European ancestry controls NA Illumina [171588] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082479 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative body size at age 10 - Thinner (UKB data field 1687) 141,504 European ancestry cases, 282,108 European ancestry controls NA Affymetrix, Illumina [541831] 0 comparative body size at age 10, self-reported http://www.ebi.ac.uk/efo/EFO_0009819 GCST90077588 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - A moderate amount (UKB data field 20460) (Gene-based burden) 36,602 European ancestry cases, 99,813 European ancestry controls NA Illumina [171588] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082480 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whole body fat mass (UKB data field 23100) 423,023 European ancestry individuals NA Affymetrix, Illumina [541784] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90078904 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - An extreme amount (UKB data field 20460) (Gene-based burden) 17,406 European ancestry cases, 119,009 European ancestry controls NA Illumina [171588] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082482 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching - Time to complete round (UKB data field 400) 423,480 European ancestry individuals NA Affymetrix, Illumina [541586] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079141 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - Not at all (UKB data field 20460) (Gene-based burden) 2,279 European ancestry cases, 134,136 European ancestry controls NA Illumina [171588] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082478 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myocardial infarction 17,896 European ancestry cases, 404,595 European ancestry controls 8,975 European ancestry cases, 98,228 European ancestry controls Affymetrix, Illumina [541387] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90081495 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Belief that own life is meaningful - Very much (UKB data field 20460) (Gene-based burden) 72,023 European ancestry cases, 64,392 European ancestry controls NA Illumina [171588] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082481 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Wheeze or whistling in the chest in last year (UKB data field 2316) 92,570 European ancestry cases, 330,651 European ancestry controls NA Affymetrix, Illumina [541354] 0 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90078934 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bilateral oophorectomy (UKB data field 2834) (Gene-based burden) 19,323 European ancestry cases, 211,189 European ancestry controls NA Illumina [181002] 0 bilateral oophorectomy http://www.ebi.ac.uk/efo/EFO_0009717 GCST90082949 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing difficulty problems background noise (UKB data field 2257) 167,296 European ancestry cases, 255,576 European ancestry controls NA Affymetrix, Illumina [541349] 1 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90078878 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Biometrics duration (UKB data field 4) (Gene-based burden) 430,604 European ancestry individuals NA Illumina [185945] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90083240 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Get mildly or occasionally tanned (UKB data field 1727) 93,163 European ancestry cases, 329,407 European ancestry controls NA Affymetrix, Illumina [540939] 4 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90077604 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Bipolar I Disorder (UKB data field 20126) (Gene-based burden) 673 European ancestry cases, 103,157 European ancestry controls NA Illumina [166400] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90082295 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Get moderately tanned (UKB data field 1727) 173,164 European ancestry cases, 249,406 European ancestry controls NA Affymetrix, Illumina [540939] 4 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90077603 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Bipolar II Disorder (UKB data field 20126) (Gene-based burden) 623 European ancestry cases, 103,207 European ancestry controls NA Illumina [166400] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90082296 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Get very tanned (UKB data field 1727) 89,584 European ancestry cases, 332,986 European ancestry controls NA Affymetrix, Illumina [540939] 6 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90077602 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - No Bipolar or Depression (UKB data field 20126) (Gene-based burden) 74,867 European ancestry cases, 28,963 European ancestry controls NA Illumina [166400] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082294 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Never tan only burn (UKB data field 1727) 75,919 European ancestry cases, 346,651 European ancestry controls NA Affymetrix, Illumina [540939] 11 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90077605 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Probable Recurrent major depression moderate (UKB data field 20126) (Gene-based burden) 13,120 European ancestry cases, 90,710 European ancestry controls NA Illumina [166400] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082298 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fed up feelings (UKB data field 1960) 176,598 European ancestry cases, 245,905 European ancestry controls NA Affymetrix, Illumina [540819] 0 feeling "fed-up" measurement http://www.ebi.ac.uk/efo/EFO_0009588 GCST90077622 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Probable Recurrent major depression severe (UKB data field 20126) (Gene-based burden) 7,594 European ancestry cases, 96,236 European ancestry controls NA Illumina [166400] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082297 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Long standing illness disability or infirmity (UKB data field 2188) 142,834 European ancestry cases, 278,602 European ancestry controls NA Affymetrix, Illumina [540102] 1 chronic disease http://www.ebi.ac.uk/efo/EFO_0009714 GCST90078850 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Single Probable major depression episode (UKB data field 20126) (Gene-based burden) 6,953 European ancestry cases, 96,877 European ancestry controls NA Illumina [166400] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082299 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mood swings (UKB data field 1920) 195,051 European ancestry cases, 226,165 European ancestry controls NA Affymetrix, Illumina [539881] 0 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST90077618 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar disorder status - Bipolar Type I Mania (UKB data field 20122) (Gene-based burden) 673 European ancestry cases, 623 European ancestry controls NA Illumina [15797] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90082292 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Worrier / anxious feelings (UKB data field 1980) 242,417 European ancestry cases, 178,089 European ancestry controls NA Affymetrix, Illumina [539374] 0 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90077624 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar disorder status - Bipolar Type II Hypomania (UKB data field 20122) (Gene-based burden) 623 European ancestry cases, 673 European ancestry controls NA Illumina [15797] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90082293 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nervous feelings (UKB data field 1970) 102,281 European ancestry cases, 318,122 European ancestry controls NA Affymetrix, Illumina [539355] 0 feeling nervous measurement http://www.ebi.ac.uk/efo/EFO_0009597 GCST90077623 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Birth weight (UKB data field 20022) (Gene-based burden) 247,016 European ancestry individuals NA Illumina [181342] 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90082237 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Guilty feelings (UKB data field 2030) 125,294 European ancestry cases, 295,085 European ancestry controls NA Affymetrix, Illumina [539185] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078395 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood pressure medication (UKB data field 6177) (Gene-based burden) 51,432 European ancestry cases, 18,041 European ancestry controls NA Illumina [153090] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90083473 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Haematocrit percentage (UKB data field 30030) 419,193 European ancestry individuals 115,971 European ancestry individuals Affymetrix, Illumina [538541] 2 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90078981 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bloody diarrhoea when IBS symptoms first began (UKB data field 21075) (Gene-based burden) 1,061 European ancestry cases, 8,491 European ancestry controls NA Illumina [75481] 0 Hematochezia http://purl.obolibrary.org/obo/HP_0002573 GCST90082824 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Red blood cell erythrocyte count (UKB data field 30010) 419,193 European ancestry individuals 115,334 European ancestry individuals Affymetrix, Illumina [538541] 4 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90078979 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Body fat percentage (UKB data field 23099) (Gene-based burden) 423,464 European ancestry individuals NA Illumina [185868] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90082889 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Haemoglobin concentration (UKB data field 30020) 419,192 European ancestry individuals 116,149 European ancestry individuals Affymetrix, Illumina [538540] 2 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90078980 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Body mass index (UKB data field 21001) (Gene-based burden) 429,633 European ancestry individuals NA Illumina [185928] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90082670 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean corpuscular haemoglobin (UKB data field 30050) 419,189 European ancestry individuals 114,860 European ancestry individuals Affymetrix, Illumina [538539] 6 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90078983 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Body mass index (UKB data field 23104) (Gene-based burden) 423,694 European ancestry individuals NA Illumina [185869] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90082893 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean corpuscular volume (UKB data field 30040) 419,192 European ancestry individuals 115,408 European ancestry individuals Affymetrix, Illumina [538539] 6 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90078982 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Born by caesarian section (UKB data field 21066) (Gene-based burden) 3,960 European ancestry cases, 142,538 European ancestry controls NA Illumina [172914] 0 cesarean section http://www.ebi.ac.uk/efo/EFO_0009636 GCST90082816 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Red blood cell erythrocyte distribution width (UKB data field 30070) 419,192 European ancestry individuals 115,121 European ancestry individuals Affymetrix, Illumina [538539] 7 Red cell distribution width http://www.ebi.ac.uk/efo/EFO_0009188 GCST90078986 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood pressure medication use (Gene-based burden) 99,813 European ancestry cases, 220,945 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90085450 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Platelet count (UKB data field 30080) 419,189 European ancestry individuals 115,119 European ancestry individuals Affymetrix, Illumina [538537] 7 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90078987 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Sometimes (UKB data field 20537) (Gene-based burden) 18,955 European ancestry cases, 23,963 European ancestry controls NA Illumina [137733] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082610 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.9: Observation for suspected disease or condition, unspecified 658 European ancestry cases, 387,272 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081192 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 500 Never (UKB data field 21028) (Gene-based burden) 12,998 European ancestry cases, 70,103 European ancestry controls NA Illumina [159594] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082683 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z08.0: Follow-up examination after surgery for malignant neoplasm 4,711 European ancestry cases, 383,219 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081197 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 501 Sometimes (UKB data field 21028) (Gene-based burden) 22,792 European ancestry cases, 60,309 European ancestry controls NA Illumina [159594] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082684 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K66.0: Peritoneal adhesions (postprocedural) (postinfection) 4,073 European ancestry cases, 383,849 European ancestry controls NA Affymetrix, Illumina [510682] 0 disease of peritoneum http://www.ebi.ac.uk/efo/EFO_0009541 GCST90080280 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Moderately unhappy (UKB data field 4526) (Gene-based burden) 6,747 European ancestry cases, 170,269 European ancestry controls NA Illumina [177117] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90083165 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T82.7: Infection and inflammatory reaction due to other cardiac and vascular devices, implants and grafts 1,068 European ancestry cases, 386,860 European ancestry controls NA Affymetrix, Illumina [510682] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081074 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Very happy (UKB data field 4526) (Gene-based burden) 73,036 European ancestry cases, 103,980 European ancestry controls NA Illumina [177117] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90083163 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.0: Mechanical complication of internal joint prosthesis 2,223 European ancestry cases, 385,699 European ancestry controls NA Affymetrix, Illumina [510682] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081078 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Very unhappy (UKB data field 4526) (Gene-based burden) 1,144 European ancestry cases, 175,872 European ancestry controls NA Illumina [177117] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90083166 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.1: Presence of aortocoronary bypass graft 5,314 European ancestry cases, 382,605 European ancestry controls 5,334 European ancestry cases, 34,104 European ancestry controls Affymetrix, Illumina [510682] 0 coronary artery bypass http://www.ebi.ac.uk/efo/EFO_0003776 GCST90081420 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High density lipoprotein cholesterol levels (UKB data field 30760) (Gene-based burden) 378,217 European ancestry individuals NA Illumina [185107] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90083017 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C19: Malignant neoplasm of rectosigmoid junction 1,074 European ancestry cases, 386,842 European ancestry controls NA Affymetrix, Illumina [510681] 0 rectosigmoid junction neoplasm http://purl.obolibrary.org/obo/MONDO_0002423 GCST90079582 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Headaches for three months (UKB data field 3799) (Gene-based burden) 40,144 European ancestry cases, 47,613 European ancestry controls NA Illumina [161836] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90083060 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.6: Hypokalemia 2,299 European ancestry cases, 385,620 European ancestry controls NA Affymetrix, Illumina [510681] 0 Hypokalemia http://purl.obolibrary.org/obo/HP_0002900 GCST90079777 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Extremely happy (UKB data field 4548) (Gene-based burden) 9,960 European ancestry cases, 167,114 European ancestry controls NA Illumina [177120] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90083174 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.8: Other forms of chronic ischemic heart disease 7,721 European ancestry cases, 380,198 European ancestry controls NA Affymetrix, Illumina [510681] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90079980 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Extremely unhappy (UKB data field 4548) (Gene-based burden) 1,794 European ancestry cases, 175,280 European ancestry controls NA Illumina [177120] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90083179 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40.9: Unilateral inguinal hernia, without obstruction or gangrene 16,831 European ancestry cases, 371,091 European ancestry controls NA Affymetrix, Illumina [510681] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90080219 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Moderately happy (UKB data field 4548) (Gene-based burden) 90,073 European ancestry cases, 87,001 European ancestry controls NA Illumina [177120] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90083176 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.1: Open wound of thumb with damage to nail 563 European ancestry cases, 387,356 European ancestry controls NA Affymetrix, Illumina [510681] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080994 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Moderately unhappy (UKB data field 4548) (Gene-based burden) 17,175 European ancestry cases, 159,899 European ancestry controls NA Illumina [177120] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90083177 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.0: Haemorrhage and haematoma complicating a procedure, not elsewhere classified (T81.0) 6,401 European ancestry cases, 381,515 European ancestry controls NA Affymetrix, Illumina [510681] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081068 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Health satisfaction - Very happy (UKB data field 4548) (Gene-based burden) 62,558 European ancestry cases, 114,516 European ancestry controls NA Illumina [177120] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90083175 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism angle right (UKB data field 5088) (Gene-based burden) 107,475 European ancestry individuals NA Illumina [167589] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90083257 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Heart disease (UKB data field 20110) 82,755 European ancestry cases, 340,932 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078272 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Atopic dermatitis (Gene-based burden) 15,131 European ancestry cases, 261,539 European ancestry controls NA Illumina [182652] 0 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90085448 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - None of the above group 1 (UKB data field 20110) 167,918 European ancestry cases, 255,769 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078281 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Atopy (Gene-based burden) 46,691 European ancestry cases, 313,235 European ancestry controls NA Illumina [184869] 0 atopy http://www.ebi.ac.uk/efo/EFO_0002686 GCST90085449 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Stroke (UKB data field 20110) 58,930 European ancestry cases, 364,757 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078273 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Visual acuity - mean spherical equivalent (UKB data field 20261) (Gene-based burden) 94,332 European ancestry individuals NA Illumina [164624] 0 visual acuity measurement http://www.ebi.ac.uk/efo/EFO_0008385 GCST90082377 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mother still alive (UKB data field 1835) 167,942 European ancestry cases, 255,745 European ancestry controls NA Affymetrix, Illumina [542060] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90077615 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - A little bit (UKB data field 20495) (Gene-based burden) 20,913 European ancestry cases, 118,564 European ancestry controls NA Illumina [172102] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90082524 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Bowel cancer (UKB data field 20110) 20,783 European ancestry cases, 402,903 European ancestry controls NA Affymetrix, Illumina [542059] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078275 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - Extremely (UKB data field 20495) (Gene-based burden) 876 European ancestry cases, 138,601 European ancestry controls NA Illumina [172102] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90082527 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Breast cancer (UKB data field 20110) 33,019 European ancestry cases, 390,667 European ancestry controls NA Affymetrix, Illumina [542059] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078276 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - Moderately (UKB data field 20495) (Gene-based burden) 4,057 European ancestry cases, 135,420 European ancestry controls NA Illumina [172102] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90082525 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - cancer (UKB data field 20110) 16,650 European ancestry cases, 407,036 European ancestry controls NA Affymetrix, Illumina [542059] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078274 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Avoided activities or situations because of previous stressful experience in past month - Quite a bit (UKB data field 20495) (Gene-based burden) 2,952 European ancestry cases, 136,525 European ancestry controls NA Illumina [172102] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90082526 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Do not know group 2 (UKB data field 20110) 21,332 European ancestry cases, 402,354 European ancestry controls NA Affymetrix, Illumina [542059] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078282 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Back pain for three months (UKB data field 3571) (Gene-based burden) 79,056 European ancestry cases, 35,975 European ancestry controls NA Illumina [168422] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90083049 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - None of the above group 2 (UKB data field 20110) 308,506 European ancestry cases, 115,180 European ancestry controls NA Affymetrix, Illumina [542059] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078283 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Basal metabolic rate (UKB data field 23105) (Gene-based burden) 423,685 European ancestry individuals NA Illumina [185869] 0 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST90082894 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Parkinsons disease (UKB data field 20110) 6,625 European ancestry cases, 417,061 European ancestry controls 1,327 European ancestry cases, 115,197 European ancestry controls Affymetrix, Illumina [542059] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078270 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractures (Gene-based burden) 27,850 European ancestry cases, 328,502 European ancestry controls NA Illumina [184796] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90085470 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.1: Surgical operation with implant of artificial internal device as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 7,633 European ancestry cases, 380,297 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081158 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Daily or almost daily (UKB data field 20416) (Gene-based burden) 4,457 European ancestry cases, 123,692 European ancestry controls NA Illumina [170195] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082422 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.2: Surgical operation with anastomosis, bypass or graft as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 2,578 European ancestry cases, 385,352 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081159 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Less than monthly (UKB data field 20416) (Gene-based burden) 31,416 European ancestry cases, 96,733 European ancestry controls NA Illumina [170195] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082419 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm predicted mass left (UKB data field 23126) 423,485 European ancestry individuals NA Affymetrix, Illumina [542169] 3 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90078929 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat free mass right (UKB data field 23121) (Gene-based burden) 423,573 European ancestry individuals NA Illumina [185869] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90082910 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Body fat percentage (UKB data field 23099) 423,464 European ancestry individuals NA Affymetrix, Illumina [542158] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90078903 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat mass left (UKB data field 23124) (Gene-based burden) 423,512 European ancestry individuals NA Illumina [185866] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90082913 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk fat percentage (UKB data field 23127) 423,451 European ancestry individuals NA Affymetrix, Illumina [542146] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90078930 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat mass right (UKB data field 23120) (Gene-based burden) 423,576 European ancestry individuals NA Illumina [185867] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90082909 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative height size at age 10 - About average (UKB data field 1697) 231,189 European ancestry cases, 192,786 European ancestry controls NA Affymetrix, Illumina [542137] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90077593 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat percentage left (UKB data field 23123) (Gene-based burden) 423,545 European ancestry individuals NA Illumina [185866] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90082912 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative height size at age 10 - Shorter (UKB data field 1697) 87,597 European ancestry cases, 336,378 European ancestry controls NA Affymetrix, Illumina [542137] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90077591 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat percentage right (UKB data field 23119) (Gene-based burden) 423,608 European ancestry individuals NA Illumina [185869] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90082908 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Comparative height size at age 10 - Taller (UKB data field 1697) 109,627 European ancestry cases, 314,348 European ancestry controls NA Affymetrix, Illumina [542137] 2 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90077592 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm predicted mass left (UKB data field 23126) (Gene-based burden) 423,485 European ancestry individuals NA Illumina [185858] 0 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90082915 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk fat mass (UKB data field 23128) 423,433 European ancestry individuals NA Affymetrix, Illumina [542129] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90078931 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm predicted mass right (UKB data field 23122) (Gene-based burden) 423,566 European ancestry individuals NA Illumina [185869] 0 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90082911 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk fat free mass (UKB data field 23129) 423,364 European ancestry individuals NA Affymetrix, Illumina [542079] 5 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90078932 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Aspartate aminotransferase levels (UKB data field 30650) (Gene-based burden) 410,630 European ancestry individuals NA Illumina [185658] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90083006 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Alzheimers disease dementia (UKB data field 20110) 38,659 European ancestry cases, 385,028 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90078269 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma (Gene-based burden) 61,807 European ancestry cases, 313,658 European ancestry controls NA Illumina [185066] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90085447 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - blood pressure (UKB data field 20110) 125,109 European ancestry cases, 298,578 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078278 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma strict (Gene-based burden) 39,436 European ancestry cases, 336,853 European ancestry controls NA Illumina [185123] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90085446 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Chronic bronchitis emphysema (UKB data field 20110) 24,686 European ancestry cases, 399,001 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078277 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma vs allergic disease (Gene-based burden) 47,628 European ancestry cases, 280,686 European ancestry controls NA Illumina [184133] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90085445 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Diabetes (UKB data field 20110) 38,129 European ancestry cases, 385,558 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078279 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Astigmatism angle left (UKB data field 5089) (Gene-based burden) 107,117 European ancestry individuals NA Illumina [167449] 0 Astigmatism http://purl.obolibrary.org/obo/HP_0000483 GCST90083258 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of mother - Do not know group 1 (UKB data field 20110) 17,882 European ancestry cases, 405,805 European ancestry controls NA Affymetrix, Illumina [542060] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078280 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.3: Surgical operation with formation of external stoma as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 544 European ancestry cases, 387,386 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081160 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Monthly (UKB data field 20416) (Gene-based burden) 11,334 European ancestry cases, 116,815 European ancestry controls NA Illumina [170195] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082420 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.4: Other reconstructive surgery as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 1,108 European ancestry cases, 386,822 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081161 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Never (UKB data field 20416) (Gene-based burden) 64,157 European ancestry cases, 63,992 European ancestry controls NA Illumina [170195] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082418 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.6: Removal of other organ (partial) (total) as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 5,438 European ancestry cases, 382,492 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081162 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of consuming six or more units of alcohol - Weekly (UKB data field 20416) (Gene-based burden) 16,785 European ancestry cases, 111,364 European ancestry controls NA Illumina [170195] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082421 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y83.8: Other surgical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 6,743 European ancestry cases, 381,187 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081163 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed days during worst episode of depression - Almost every day (UKB data field 20439) (Gene-based burden) 39,262 European ancestry cases, 37,398 European ancestry controls NA Illumina [157121] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082449 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84: Other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 3,036 European ancestry cases, 384,894 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081169 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed days during worst episode of depression - Every day (UKB data field 20439) (Gene-based burden) 29,547 European ancestry cases, 47,113 European ancestry controls NA Illumina [157121] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082450 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84.2: Radiological procedure and radiotherapy as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 654 European ancestry cases, 387,276 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081166 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed days during worst episode of depression - Less often (UKB data field 20439) (Gene-based burden) 7,851 European ancestry cases, 68,809 European ancestry controls NA Illumina [157121] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082448 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84.6: Urinary catheterization as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 534 European ancestry cases, 387,396 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081167 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed mood in last 2 weeks - More than half the days (UKB data field 2050) (Gene-based burden) 12,239 European ancestry cases, 401,330 European ancestry controls NA Illumina [185661] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082561 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y84.8: Other medical procedures as the cause of abnormal reaction of the patient, or of later complication, without mention of misadventure at the time of the procedure 1,150 European ancestry cases, 386,780 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081168 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed mood in last 2 weeks - Nearly every day (UKB data field 2050) (Gene-based burden) 7,997 European ancestry cases, 405,572 European ancestry controls NA Illumina [185661] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082562 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y86: Sequelae of other accidents 1,101 European ancestry cases, 386,829 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081170 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed mood in last 2 weeks - Several days (UKB data field 2050) (Gene-based burden) 81,404 European ancestry cases, 332,165 European ancestry controls NA Illumina [185661] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082560 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z00: Encounter for general examination without complaint, suspected or reported diagnosis 929 European ancestry cases, 387,001 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081179 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Never (UKB data field 20537) (Gene-based burden) 608 European ancestry cases, 42,310 European ancestry controls NA Illumina [137733] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082608 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.1: Observation for suspected malignant neoplasm 868 European ancestry cases, 387,062 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081188 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Often (UKB data field 20537) (Gene-based burden) 18,917 European ancestry cases, 24,001 European ancestry controls NA Illumina [137733] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082611 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.4: Observation for suspected myocardial infarction 2,726 European ancestry cases, 385,204 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081189 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of difficulty controlling worry during worst period of anxiety - Rarely (UKB data field 20537) (Gene-based burden) 4,438 European ancestry cases, 38,480 European ancestry controls NA Illumina [137733] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082609 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.8: Encounter for observation for other suspected diseases and conditions ruled out 7,113 European ancestry cases, 380,817 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081191 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95: Streptococcus, Staphylococcus, and Enterococcus as the cause of diseases classified elsewhere 5,108 European ancestry cases, 382,689 European ancestry controls NA Affymetrix, Illumina [510564] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079564 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.31: Type 2 diabetes mellitus with unspecified diabetic retinopathy (Gene-based burden) 2,622 European ancestry cases, 383,255 European ancestry controls NA Illumina [185320] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083721 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K86: Other diseases of pancreas 1,601 European ancestry cases, 386,179 European ancestry controls NA Affymetrix, Illumina [510564] 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90080313 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.319.: Type 2 diabetes mellitus with unspecified diabetic retinopathy without macular edema (Gene-based burden) 2,563 European ancestry cases, 383,369 European ancestry controls NA Illumina [185321] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083720 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.9: Malignant neoplasm of colon, unspecified 1,360 European ancestry cases, 386,429 European ancestry controls 1,070 European ancestry cases, 122,068 European ancestry controls Affymetrix, Illumina [510563] 0 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90079580 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.32: Type 2 diabetes mellitus with mild nonproliferative diabetic retinopathy (Gene-based burden) 926 European ancestry cases, 385,625 European ancestry controls NA Illumina [185318] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083724 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35.0: Sicca syndrome 711 European ancestry cases, 387,080 European ancestry controls NA Affymetrix, Illumina [510561] 0 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90080468 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.329.: Type 2 diabetes mellitus with mild nonproliferative diabetic retinopathy without macular edema (Gene-based burden) 926 European ancestry cases, 385,625 European ancestry controls NA Illumina [185318] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083723 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33.3: Retinal breaks without detachment 1,191 European ancestry cases, 386,593 European ancestry controls NA Affymetrix, Illumina [510558] 0 retinal break http://www.ebi.ac.uk/efo/EFO_0010698 GCST90079896 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.329.9: Type 2 diabetes mellitus with mild nonproliferative diabetic retinopathy without macular edema, unspecified eye (Gene-based burden) 926 European ancestry cases, 385,625 European ancestry controls NA Illumina [185318] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083722 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K02: Dental caries 3,818 European ancestry cases, 383,967 European ancestry controls NA Affymetrix, Illumina [510556] 0 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST90080165 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.4: Type 2 diabetes mellitus with neurological complications (Gene-based burden) 751 European ancestry cases, 386,815 European ancestry controls NA Illumina [185341] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083726 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E89: Postprocedural endocrine and metabolic complications and disorders, not elsewhere classified 1,804 European ancestry cases, 385,989 European ancestry controls NA Affymetrix, Illumina [510555] 0 metabolic disease http://www.ebi.ac.uk/efo/EFO_0000589 GCST90079782 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.9: Type 2 diabetes mellitus without complications (Gene-based burden) 26,590 European ancestry cases, 359,248 European ancestry controls NA Illumina [185312] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083727 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.1: Fracture of upper end of tibia 762 European ancestry cases, 387,022 European ancestry controls NA Affymetrix, Illumina [510555] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081019 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13: Other specified diabetes mellitus (Gene-based burden) 8,836 European ancestry cases, 377,872 European ancestry controls NA Illumina [185332] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90083732 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L02.2: Cutaneous abscess, furuncle and carbuncle of trunk 1,025 European ancestry cases, 386,749 European ancestry controls NA Affymetrix, Illumina [510554] 0 Cutaneous abscess http://purl.obolibrary.org/obo/HP_0031292 GCST90080324 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13.6: Other specified diabetes mellitus with other specified complications (Gene-based burden) 8,624 European ancestry cases, 378,107 European ancestry controls NA Illumina [185332] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90083731 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.3: Trigger finger 3,155 European ancestry cases, 384,623 European ancestry controls NA Affymetrix, Illumina [510553] 0 stenosing tenosynovitis http://www.ebi.ac.uk/efo/EFO_0010822 GCST90080517 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13.62: Other specified diabetes mellitus with skin complications (Gene-based burden) 8,622 European ancestry cases, 378,109 European ancestry controls NA Illumina [185332] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90083730 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I65: Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction 1,329 European ancestry cases, 386,456 European ancestry controls NA Affymetrix, Illumina [510552] 0 occlusion precerebral artery http://www.ebi.ac.uk/efo/EFO_0009677 GCST90080038 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13.621.: Other specified diabetes mellitus with foot ulcer (Gene-based burden) 8,622 European ancestry cases, 378,109 European ancestry controls NA Illumina [185332] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90083729 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.8: Other symptoms and signs involving the genitourinary system 3,897 European ancestry cases, 383,861 European ancestry controls NA Affymetrix, Illumina [510552] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90080850 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E14: Unspecified diabetes mellitus (Gene-based burden) 3,469 European ancestry cases, 384,252 European ancestry controls NA Illumina [185344] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90083734 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D35: Benign neoplasm of other and unspecified endocrine glands 1,177 European ancestry cases, 386,605 European ancestry controls NA Affymetrix, Illumina [510550] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079693 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C67: Malignant neoplasm of bladder 2,670 European ancestry cases, 385,138 European ancestry controls NA Affymetrix, Illumina [510582] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90079612 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D64: Other anemias (Gene-based burden) 15,647 European ancestry cases, 369,231 European ancestry controls NA Illumina [185295] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90083698 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I31: Other diseases of pericardium 1,596 European ancestry cases, 386,216 European ancestry controls NA Affymetrix, Illumina [510582] 0 pericarditis http://www.ebi.ac.uk/efo/EFO_0007427 GCST90079990 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D64.9: Anemia, unspecified (Gene-based burden) 14,923 European ancestry cases, 372,152 European ancestry controls NA Illumina [185340] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90083697 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E21.3: Hyperparathyroidism, unspecified 512 European ancestry cases, 387,308 European ancestry controls 1,146 European ancestry cases, 112,967 European ancestry controls Affymetrix, Illumina [510581] 0 hyperparathyroidism http://www.ebi.ac.uk/efo/EFO_0008506 GCST90079752 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D68: Other coagulation defects (Gene-based burden) 1,286 European ancestry cases, 386,192 European ancestry controls NA Illumina [185338] 0 blood coagulation disease http://www.ebi.ac.uk/efo/EFO_0009314 GCST90083699 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.5: Fracture of pubis 662 European ancestry cases, 387,126 European ancestry controls NA Affymetrix, Illumina [510581] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080969 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D69: Purpura and other hemorrhagic conditions (Gene-based burden) 2,456 European ancestry cases, 384,489 European ancestry controls NA Illumina [185324] 0 hemorrhagic disease http://purl.obolibrary.org/obo/MONDO_0002243 GCST90083701 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E86: Volume depletion 4,194 European ancestry cases, 383,606 European ancestry controls NA Affymetrix, Illumina [510580] 0 Hypovolemia http://purl.obolibrary.org/obo/HP_0011106 GCST90079773 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D69.6: Thrombocytopenia, unspecified (Gene-based burden) 1,788 European ancestry cases, 385,791 European ancestry controls NA Illumina [185337] 0 Thrombocytopenia http://purl.obolibrary.org/obo/HP_0001873 GCST90083700 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M87: Osteonecrosis 669 European ancestry cases, 387,134 European ancestry controls NA Affymetrix, Illumina [510580] 0 osteonecrosis http://www.ebi.ac.uk/efo/EFO_0004259 GCST90080565 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D70: Neutropenia (Gene-based burden) 4,407 European ancestry cases, 382,668 European ancestry controls NA Illumina [185330] 0 neutropenia http://purl.obolibrary.org/obo/MONDO_0001475 GCST90083702 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y04: Assault by bodily force 809 European ancestry cases, 386,995 European ancestry controls NA Affymetrix, Illumina [510579] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081147 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D72: Other disorders of white blood cells (Gene-based burden) 691 European ancestry cases, 386,364 European ancestry controls NA Illumina [185324] 0 leukocyte disorder http://purl.obolibrary.org/obo/MONDO_0004805 GCST90083703 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M05: Rheumatoid arthritis with rheumatoid factor 769 European ancestry cases, 387,034 European ancestry controls NA Affymetrix, Illumina [510578] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90080387 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D73: Diseases of spleen (Gene-based burden) 692 European ancestry cases, 387,204 European ancestry controls NA Illumina [185344] 0 splenic disease http://www.ebi.ac.uk/efo/EFO_0009002 GCST90083704 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.0: Presence of cardiac pacemaker 3,224 European ancestry cases, 384,575 European ancestry controls NA Affymetrix, Illumina [510578] 0 artificial cardiac pacemaker http://www.ebi.ac.uk/efo/EFO_0009719 GCST90081419 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D75: Other and unspecified diseases of blood and blood-forming organs (Gene-based burden) 993 European ancestry cases, 386,043 European ancestry controls NA Illumina [185330] 0 hematologic disease http://www.ebi.ac.uk/efo/EFO_0005803 GCST90083705 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04.5: Stenosis and insufficiency of lacrimal passages 1,351 European ancestry cases, 386,444 European ancestry controls NA Affymetrix, Illumina [510577] 0 lacrimal apparatus disease http://www.ebi.ac.uk/efo/EFO_0009455 GCST90079877 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D86: sarcoidosis (Gene-based burden) 782 European ancestry cases, 386,780 European ancestry controls NA Illumina [185339] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90083706 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25: Age-related cataract 12,614 European ancestry cases, 375,168 European ancestry controls 14,357 European ancestry cases, 100,935 European ancestry controls Affymetrix, Illumina [510577] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90079889 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E03: Other hypothyroidism (Gene-based burden) 21,010 European ancestry cases, 362,055 European ancestry controls NA Illumina [185246] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90083708 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T43.2: Poisoning by, adverse effect of and underdosing of other and unspecified antidepressants 774 European ancestry cases, 387,027 European ancestry controls NA Affymetrix, Illumina [510577] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081055 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E03.9: Hypothyroidism, unspecified (Gene-based burden) 19,694 European ancestry cases, 365,664 European ancestry controls NA Illumina [185290] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90083707 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R03.1: Nonspecific low blood-pressure reading 1,483 European ancestry cases, 386,299 European ancestry controls NA Affymetrix, Illumina [510575] 0 Abnormal systemic blood pressure http://purl.obolibrary.org/obo/HP_0030972 GCST90080759 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E14.9: Unspecified diabetes mellitus without complications (Gene-based burden) 3,071 European ancestry cases, 384,859 European ancestry controls NA Illumina [185344] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90083733 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49.9: Cardiac arrhythmia, unspecified 1,299 European ancestry cases, 386,472 European ancestry controls NA Affymetrix, Illumina [510550] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90080018 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E16: Other disorders of pancreatic internal secretion (Gene-based burden) 1,620 European ancestry cases, 385,084 European ancestry controls NA Illumina [185329] 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90083736 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I61: Nontraumatic intracerebral hemorrhage 1,085 European ancestry cases, 386,689 European ancestry controls NA Affymetrix, Illumina [510550] 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90080031 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E16.2: Hypoglycemia, unspecified (Gene-based burden) 1,319 European ancestry cases, 386,316 European ancestry controls NA Illumina [185335] 0 Hypoglycemia http://purl.obolibrary.org/obo/HP_0001943 GCST90083735 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I38: Endocarditis, valve unspecified 572 European ancestry cases, 387,181 European ancestry controls NA Affymetrix, Illumina [510549] 0 endocarditis http://www.ebi.ac.uk/efo/EFO_0000465 GCST90079997 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E21: Hyperparathyroidism and other disorders of parathyroid gland (Gene-based burden) 1,168 European ancestry cases, 386,457 European ancestry controls NA Illumina [185341] 0 hyperparathyroidism http://www.ebi.ac.uk/efo/EFO_0008506 GCST90083739 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M00: Pyogenic arthritis 508 European ancestry cases, 387,264 European ancestry controls NA Affymetrix, Illumina [510548] 0 infectious arthritis http://www.ebi.ac.uk/efo/EFO_1001351 GCST90080385 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E21.0: Primary hyperparathyroidism (Gene-based burden) 643 European ancestry cases, 387,287 European ancestry controls NA Illumina [185344] 0 primary hyperparathyroidism http://www.ebi.ac.uk/efo/EFO_0008519 GCST90083737 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D03: Melanoma in situ 969 European ancestry cases, 386,791 European ancestry controls NA Affymetrix, Illumina [510547] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079644 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E21.3: Hyperparathyroidism, unspecified (Gene-based burden) 512 European ancestry cases, 387,308 European ancestry controls NA Illumina [185344] 0 hyperparathyroidism http://www.ebi.ac.uk/efo/EFO_0008506 GCST90083738 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G35: Multiple sclerosis 1,634 European ancestry cases, 386,134 European ancestry controls NA Affymetrix, Illumina [510547] 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90079822 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E23: Hypofunction and other disorders of the pituitary gland (Gene-based burden) 566 European ancestry cases, 387,112 European ancestry controls NA Illumina [185342] 0 pituitary gland disease http://www.ebi.ac.uk/efo/EFO_0009607 GCST90083740 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M31: Other necrotizing vasculopathies 855 European ancestry cases, 386,913 European ancestry controls NA Affymetrix, Illumina [510547] 0 vasculitis http://www.ebi.ac.uk/efo/EFO_0006803 GCST90080467 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E27: Other disorders of adrenal gland (Gene-based burden) 649 European ancestry cases, 387,197 European ancestry controls NA Illumina [185344] 0 adrenal gland disease http://www.ebi.ac.uk/efo/EFO_0005539 GCST90083741 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.9: Disorder of urinary system, unspecified 688 European ancestry cases, 387,084 European ancestry controls NA Affymetrix, Illumina [510547] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90080615 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E28: Ovarian dysfunction (Gene-based burden) 500 European ancestry cases, 210,556 European ancestry controls NA Illumina [179878] 0 ovarian dysfunction http://www.ebi.ac.uk/efo/EFO_0009003 GCST90083742 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K74: Fibrosis and cirrhosis of liver 1,292 European ancestry cases, 386,463 European ancestry controls NA Affymetrix, Illumina [510546] 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90080286 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E53: Deficiency of other B group vitamins (Gene-based burden) 1,552 European ancestry cases, 384,821 European ancestry controls NA Illumina [185328] 0 disorder of other vitamins and cofactors metabolism and transport http://purl.obolibrary.org/obo/MONDO_0017760 GCST90083744 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M18: Osteoarthritis of first carpometacarpal joint 1,788 European ancestry cases, 385,989 European ancestry controls NA Affymetrix, Illumina [510546] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080418 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E53.8: Deficiency of other specified B group vitamins (Gene-based burden) 1,075 European ancestry cases, 386,854 European ancestry controls NA Illumina [185344] 0 disorder of other vitamins and cofactors metabolism and transport http://purl.obolibrary.org/obo/MONDO_0017760 GCST90083743 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.4: Other hammer toe(s) (acquired) 2,366 European ancestry cases, 385,393 European ancestry controls NA Affymetrix, Illumina [510546] 0 Hammer Toe Syndrome http://www.ebi.ac.uk/efo/EFO_1001336 GCST90080430 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Less than 15 minutes (UKB data field 981) (Gene-based burden) 5,397 European ancestry cases, 307,380 European ancestry controls NA Illumina [183664] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083511 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G57.6: Lesion of plantar nerve 1,560 European ancestry cases, 386,370 European ancestry controls NA Affymetrix, Illumina [510688] 0 peripheral nerve lesion http://purl.obolibrary.org/obo/MONDO_0024334 GCST90079847 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 30 minutes and 1 hour (UKB data field 981) (Gene-based burden) 121,322 European ancestry cases, 191,455 European ancestry controls NA Illumina [183664] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083513 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Never (UKB data field 20409) (Gene-based burden) 61,509 European ancestry cases, 15,078 European ancestry controls NA Illumina [156091] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082399 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.3: Blood transfusion without reported diagnosis 1,195 European ancestry cases, 386,735 European ancestry controls NA Affymetrix, Illumina [510688] 1 blood transfusion http://www.ebi.ac.uk/efo/EFO_0020988 GCST90081281 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Weekly (UKB data field 20409) (Gene-based burden) 1,670 European ancestry cases, 74,917 European ancestry controls NA Illumina [156091] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082402 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.4: Preparatory care for subsequent treatment, not elsewhere classified 1,733 European ancestry cases, 386,197 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081282 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04.2: Nontoxic multinodular goiter (Gene-based burden) 815 European ancestry cases, 387,115 European ancestry controls NA Illumina [185344] 0 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90083710 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.7: Left bundle-branch block, unspecified 2,509 European ancestry cases, 385,261 European ancestry controls NA Affymetrix, Illumina [510570] 0 Left bundle branch block http://purl.obolibrary.org/obo/HP_0011713 GCST90080004 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04.9: Nontoxic goiter, unspecified (Gene-based burden) 651 European ancestry cases, 387,279 European ancestry controls NA Illumina [185344] 0 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90083711 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31.7: Polyp of stomach and duodenum 6,198 European ancestry cases, 381,584 European ancestry controls 343 European ancestry cases, 97,677 European ancestry controls Affymetrix, Illumina [510570] 0 stomach polyp http://purl.obolibrary.org/obo/MONDO_0008277 GCST90080210 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05: Thyrotoxicosis [hyperthyroidism] (Gene-based burden) 3,102 European ancestry cases, 383,241 European ancestry controls NA Illumina [185325] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90083716 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z22: Carrier of infectious disease 1,553 European ancestry cases, 386,247 European ancestry controls NA Affymetrix, Illumina [510570] 0 carrier status http://www.ebi.ac.uk/efo/EFO_0007658 GCST90081222 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05.0: Thyrotoxicosis with diffuse goiter (Gene-based burden) 565 European ancestry cases, 387,358 European ancestry controls NA Illumina [185343] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90083713 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M15.9: Polyosteoarthritis, unspecified 5,066 European ancestry cases, 382,725 European ancestry controls NA Affymetrix, Illumina [510569] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080407 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05.9: Thyrotoxicosis, unspecified (Gene-based burden) 2,203 European ancestry cases, 384,824 European ancestry controls NA Illumina [185334] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90083715 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W18: Other slipping, tripping and stumbling and falls 2,627 European ancestry cases, 385,170 European ancestry controls NA Affymetrix, Illumina [510568] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081115 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05.90: Thyrotoxicosis, unspecified without thyrotoxic crisis or storm (Gene-based burden) 529 European ancestry cases, 386,362 European ancestry controls NA Illumina [185326] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90083714 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.9: Disease of esophagus, unspecified 690 European ancestry cases, 387,136 European ancestry controls NA Affymetrix, Illumina [510567] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90080194 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E10: Type 1 diabetes mellitus (Gene-based burden) 3,971 European ancestry cases, 383,232 European ancestry controls NA Illumina [185330] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90083719 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R16.1: Splenomegaly, not elsewhere classified 515 European ancestry cases, 387,283 European ancestry controls 746 European ancestry cases, 75,109 European ancestry controls Affymetrix, Illumina [510567] 1 Splenomegaly http://purl.obolibrary.org/obo/HP_0001744 GCST90080804 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E10.3: Type 1 diabetes mellitus with ophthalmic complications (Gene-based burden) 587 European ancestry cases, 387,305 European ancestry controls NA Illumina [185344] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90083717 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50.9: Iron deficiency anemia, unspecified 7,982 European ancestry cases, 379,813 European ancestry controls NA Affymetrix, Illumina [510566] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90079703 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E10.9: Type 1 diabetes mellitus without complications (Gene-based burden) 3,628 European ancestry cases, 383,813 European ancestry controls NA Illumina [185338] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90083718 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N21: Calculus of lower urinary tract 979 European ancestry cases, 386,821 European ancestry controls NA Affymetrix, Illumina [510566] 0 ureterolithiasis http://www.ebi.ac.uk/efo/EFO_1001228 GCST90080590 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11: Type 2 diabetes mellitus (Gene-based burden) 27,324 European ancestry cases, 357,976 European ancestry controls NA Illumina [185306] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083728 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K66: Other disorders of peritoneum 4,357 European ancestry cases, 383,442 European ancestry controls NA Affymetrix, Illumina [510565] 0 disease of peritoneum http://www.ebi.ac.uk/efo/EFO_0009541 GCST90080281 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.3: Type 2 diabetes mellitus with ophthalmic complications (Gene-based burden) 4,180 European ancestry cases, 381,289 European ancestry controls NA Illumina [185310] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90083725 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Over six months but less than 12 months (UKB data field 20438) (Gene-based burden) 11,994 European ancestry cases, 67,181 European ancestry controls NA Illumina [158132] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90082445 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.0: Mental and behavioural disorders due to use of alcohol, acute intoxication 2,064 European ancestry cases, 385,866 European ancestry controls NA Affymetrix, Illumina [510688] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90079787 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Over three months but less than six months (UKB data field 20438) (Gene-based burden) 14,051 European ancestry cases, 65,124 European ancestry controls NA Illumina [158132] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90082444 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.3: Mental and behavioural disorders due to use of alcohol, withdrawal state 847 European ancestry cases, 387,083 European ancestry controls NA Affymetrix, Illumina [510688] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90079791 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Over two years (UKB data field 20438) (Gene-based burden) 7,396 European ancestry cases, 71,779 European ancestry controls NA Illumina [158132] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90082447 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.1: Mental and behavioural disorders due to use of tobacco, harmful use 14,902 European ancestry cases, 373,028 European ancestry controls NA Affymetrix, Illumina [510688] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90079794 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration to complete alphanumeric path trail 2 (UKB data field 20157) (Gene-based burden) 92,685 European ancestry individuals NA Illumina [162392] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082309 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.2: Mixed anxiety and depressive disorder 2,046 European ancestry cases, 385,884 European ancestry controls NA Affymetrix, Illumina [510688] 0 mixed anxiety and depressive disorder http://purl.obolibrary.org/obo/MONDO_0041086 GCST90079810 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration to complete numeric path trail 1 (UKB data field 20156) (Gene-based burden) 92,687 European ancestry individuals NA Illumina [162392] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082308 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40.3: Generalized idiopathic epilepsy and epileptic syndromes 510 European ancestry cases, 387,420 European ancestry controls NA Affymetrix, Illumina [510688] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90079823 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Symbol digit substitution - Duration to entering value (UKB data field 20230) (Gene-based burden) 105,636 European ancestry individuals NA Illumina [165850] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082360 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G50.0: Trigeminal neuralgia 502 European ancestry cases, 387,428 European ancestry controls NA Affymetrix, Illumina [510688] 0 trigeminal neuralgia http://www.ebi.ac.uk/efo/EFO_1001219 GCST90079836 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reaction time - Duration to first press of snap button in each round (UKB data field 404) (Gene-based burden) 428,085 European ancestry individuals NA Illumina [185922] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083129 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55.1: Nerve root and plexus compressions in intervertebral disc disorders 4,336 European ancestry cases, 383,594 European ancestry controls NA Affymetrix, Illumina [510688] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90079841 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration visual acuity screen displayed left (UKB data field 5188) (Gene-based burden) 110,648 European ancestry individuals NA Illumina [168349] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90083312 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55.2: Nerve root and plexus compressions in spondylosis 662 European ancestry cases, 387,268 European ancestry controls NA Affymetrix, Illumina [510688] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90079842 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration visual acuity screen displayed right (UKB data field 5186) (Gene-based burden) 110,647 European ancestry individuals NA Illumina [168347] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90083311 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56.0: Carpal tunnel syndrome 11,271 European ancestry cases, 376,659 European ancestry controls NA Affymetrix, Illumina [510688] 0 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90079844 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 15 and 30 minutes (UKB data field 981) (Gene-based burden) 69,233 European ancestry cases, 243,544 European ancestry controls NA Illumina [183664] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083512 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56.2: Lesion of ulnar nerve 1,388 European ancestry cases, 386,542 European ancestry controls NA Affymetrix, Illumina [510688] 0 ulnar nerve lesion http://purl.obolibrary.org/obo/MONDO_0001458 GCST90079845 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.9: Care involving use of rehabilitation procedure, unspecified 906 European ancestry cases, 387,024 European ancestry controls NA Affymetrix, Illumina [510688] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081276 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Less than monthly (UKB data field 20409) (Gene-based burden) 10,792 European ancestry cases, 65,795 European ancestry controls NA Illumina [156091] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082400 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.0: Encounter for antineoplastic radiation therapy 2,775 European ancestry cases, 385,155 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081278 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Monthly (UKB data field 20409) (Gene-based burden) 2,026 European ancestry cases, 74,561 European ancestry controls NA Illumina [156091] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082401 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.2: Other chemotherapy 12,384 European ancestry cases, 375,546 European ancestry controls NA Affymetrix, Illumina [510688] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081280 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D41.4: Neoplasm of uncertain behavior of bladder (Gene-based burden) 751 European ancestry cases, 387,179 European ancestry controls NA Illumina [185324] 0 GCST90083683 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85: Complications of other internal prosthetic devices, implants and grafts 2,918 European ancestry cases, 384,896 European ancestry controls NA Affymetrix, Illumina [510592] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081087 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D47: Other neoplasms of uncertain behavior of lymphoid, hematopoietic and related tissue (Gene-based burden) 987 European ancestry cases, 386,440 European ancestry controls NA Illumina [185336] 0 GCST90083685 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.5: Personal history of self-harm 1,490 European ancestry cases, 386,331 European ancestry controls NA Affymetrix, Illumina [510591] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081399 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D48: Neoplasm of uncertain behavior of other and unspecified sites (Gene-based burden) 988 European ancestry cases, 386,500 European ancestry controls NA Illumina [185340] 0 GCST90083686 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.10: Unspecified fracture of upper end of tibia 612 European ancestry cases, 387,202 European ancestry controls NA Affymetrix, Illumina [510590] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081018 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50: Iron deficiency anemia (Gene-based burden) 12,317 European ancestry cases, 370,728 European ancestry controls NA Illumina [185267] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90083690 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S80.9: Unspecified superficial injury of knee and lower leg 532 European ancestry cases, 387,297 European ancestry controls NA Affymetrix, Illumina [510589] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081015 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50.0: Iron deficiency anemia secondary to blood loss (chronic) (Gene-based burden) 600 European ancestry cases, 387,139 European ancestry controls NA Illumina [185330] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90083687 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03: Encounter for medical observation for suspected diseases and conditions ruled out 12,954 European ancestry cases, 374,871 European ancestry controls NA Affymetrix, Illumina [510589] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081193 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50.8: Other iron deficiency anemias (Gene-based burden) 3,248 European ancestry cases, 384,682 European ancestry controls NA Illumina [185344] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90083688 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F20: Schizophrenia 741 European ancestry cases, 387,059 European ancestry controls NA Affymetrix, Illumina [510588] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90079800 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50.9: Iron deficiency anemia, unspecified (Gene-based burden) 7,982 European ancestry cases, 379,813 European ancestry controls NA Illumina [185342] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90083689 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I46: Cardiac arrest 1,488 European ancestry cases, 386,316 European ancestry controls NA Affymetrix, Illumina [510586] 0 GCST90080010 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D51: Vitamin B12 deficiency anemia (Gene-based burden) 1,370 European ancestry cases, 385,838 European ancestry controls NA Illumina [185339] 0 vitamin B12 deficiency http://www.ebi.ac.uk/efo/EFO_0000734 GCST90083692 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z89: Acquired absence of limb 626 European ancestry cases, 387,200 European ancestry controls NA Affymetrix, Illumina [510586] 0 amputation http://www.ebi.ac.uk/efo/EFO_0009632 GCST90081389 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D51.0: Vitamin B12 deficiency anemia due to intrinsic factor deficiency (Gene-based burden) 963 European ancestry cases, 386,967 European ancestry controls NA Illumina [185344] 0 vitamin B12 deficiency http://www.ebi.ac.uk/efo/EFO_0000734 GCST90083691 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C20: Malignant neoplasm of rectum 1,884 European ancestry cases, 385,913 European ancestry controls NA Affymetrix, Illumina [510585] 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90079583 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D61: Other aplastic anemias and other bone marrow failure syndromes (Gene-based burden) 645 European ancestry cases, 387,116 European ancestry controls NA Illumina [185343] 0 bone marrow failure syndrome, anemia (phenotype) http://purl.obolibrary.org/obo/MONDO_0000159, http://www.ebi.ac.uk/efo/EFO_0004272 GCST90083694 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83.9: Asymptomatic varicose veins of lower extremities 11,767 European ancestry cases, 376,048 European ancestry controls 2,486 European ancestry cases, 107,805 European ancestry controls Affymetrix, Illumina [510584] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90080065 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D61.9: Aplastic anemia, unspecified (Gene-based burden) 572 European ancestry cases, 387,353 European ancestry controls NA Illumina [185343] 0 Aplastic anemia http://purl.obolibrary.org/obo/HP_0001915 GCST90083693 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30.1: Allergic rhinitis due to pollen 1,201 European ancestry cases, 386,622 European ancestry controls NA Affymetrix, Illumina [510583] 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90080102 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D63.0: Anemia in neoplastic disease (Gene-based burden) 535 European ancestry cases, 387,395 European ancestry controls NA Illumina [185344] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90083695 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T42: Poisoning by, adverse effect of and underdosing of antiepileptic, sedative- hypnotic and antiparkinsonism drugs 1,043 European ancestry cases, 386,755 European ancestry controls NA Affymetrix, Illumina [510583] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081054 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D63.165.8: Anemia in chronic kidney disease (Gene-based burden) 936 European ancestry cases, 386,949 European ancestry controls NA Illumina [185344] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90083696 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50.8: Other iron deficiency anemias 3,248 European ancestry cases, 384,682 European ancestry controls NA Affymetrix, Illumina [510688] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90079702 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Quite distressing (UKB data field 20462) (Gene-based burden) 636 European ancestry cases, 6,075 European ancestry controls NA Illumina [61877] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082486 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D51.0: Vitamin B12 deficiency anemia due to intrinsic factor deficiency 963 European ancestry cases, 386,967 European ancestry controls NA Affymetrix, Illumina [510688] 0 vitamin B12 deficiency http://www.ebi.ac.uk/efo/EFO_0000734 GCST90079705 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Very distressing (UKB data field 20462) (Gene-based burden) 803 European ancestry cases, 5,908 European ancestry controls NA Illumina [61877] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082487 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D63.0: Anemia in neoplastic disease 535 European ancestry cases, 387,395 European ancestry controls NA Affymetrix, Illumina [510688] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90079709 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Doctor restricts physical activity due to heart condition (UKB data field 6014) (Gene-based burden) 3,441 European ancestry cases, 77,630 European ancestry controls NA Illumina [160009] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083391 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04.2: Nontoxic multinodular goiter 815 European ancestry cases, 387,115 European ancestry controls NA Affymetrix, Illumina [510688] 0 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90079724 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Retinal optical coherence tomography - duration at which OCT screen shown left (UKB data field 6073) (Gene-based burden) 81,113 European ancestry individuals NA Illumina [159963] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083408 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04.9: Nontoxic goiter, unspecified 651 European ancestry cases, 387,279 European ancestry controls NA Affymetrix, Illumina [510688] 0 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90079725 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Autorefraction - Duration at which refractometer first shown left (UKB data field 5193) (Gene-based burden) 109,455 European ancestry individuals NA Illumina [168079] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083314 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E14.9: Unspecified diabetes mellitus without complications 3,071 European ancestry cases, 384,859 European ancestry controls NA Affymetrix, Illumina [510688] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90079747 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Autorefraction - Duration at which refractometer first shown right (UKB data field 5190) (Gene-based burden) 109,455 European ancestry individuals NA Illumina [168073] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083313 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E21.0: Primary hyperparathyroidism 643 European ancestry cases, 387,287 European ancestry controls 933 European ancestry cases, 112,967 European ancestry controls Affymetrix, Illumina [510688] 0 primary hyperparathyroidism http://www.ebi.ac.uk/efo/EFO_0008519 GCST90079751 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of moderate activity (UKB data field 894) (Gene-based burden) 327,407 European ancestry individuals NA Illumina [184052] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083491 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E53.8: Deficiency of other specified B group vitamins 1,075 European ancestry cases, 386,854 European ancestry controls NA Affymetrix, Illumina [510688] 0 disorder of other vitamins and cofactors metabolism and transport http://purl.obolibrary.org/obo/MONDO_0017760 GCST90079757 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of vigorous activity (UKB data field 914) (Gene-based burden) 242,729 European ancestry individuals NA Illumina [180979] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083494 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E66.8: Other obesity 2,009 European ancestry cases, 385,921 European ancestry controls NA Affymetrix, Illumina [510688] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90079762 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of walks (UKB data field 874) (Gene-based burden) 372,854 European ancestry individuals NA Illumina [185080] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083489 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78.5: Hyperlipidemia, unspecified 6,517 European ancestry cases, 381,413 European ancestry controls NA Affymetrix, Illumina [510688] 0 hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0021187 GCST90079767 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Between one and three months (UKB data field 20438) (Gene-based burden) 24,189 European ancestry cases, 54,986 European ancestry controls NA Illumina [158132] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90082443 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E83.4: Disorders of magnesium metabolism 684 European ancestry cases, 387,246 European ancestry controls NA Affymetrix, Illumina [510688] 0 mineral metabolism disease http://www.ebi.ac.uk/efo/EFO_0009556 GCST90079770 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Less than a month (UKB data field 20438) (Gene-based burden) 11,829 European ancestry cases, 67,346 European ancestry controls NA Illumina [158132] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90082442 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.7: Fluid overload 804 European ancestry cases, 387,126 European ancestry controls NA Affymetrix, Illumina [510688] 0 Hypervolemia http://purl.obolibrary.org/obo/HP_0011105 GCST90079778 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - One to two years (UKB data field 20438) (Gene-based burden) 8,427 European ancestry cases, 70,748 European ancestry controls NA Illumina [158132] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90082446 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E89.0: Postprocedural hypothyroidism 1,439 European ancestry cases, 386,491 European ancestry controls NA Affymetrix, Illumina [510688] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90079781 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G63.2: Diabetic polyneuropathy 538 European ancestry cases, 387,392 European ancestry controls NA Affymetrix, Illumina [510688] 0 diabetic polyneuropathy http://purl.obolibrary.org/obo/MONDO_0001583 GCST90079851 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 1 and 1.5 hours (UKB data field 981) (Gene-based burden) 62,226 European ancestry cases, 250,551 European ancestry controls NA Illumina [183664] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083514 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G99.2: Myelopathy in diseases classified elsewhere 1,259 European ancestry cases, 386,671 European ancestry controls NA Affymetrix, Illumina [510688] 0 Myelopathy http://purl.obolibrary.org/obo/HP_0002196 GCST90079860 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 1 5 and 2 hours (UKB data field 981) (Gene-based burden) 31,911 European ancestry cases, 280,866 European ancestry controls NA Illumina [183664] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083515 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H00.1: Chalazion 1,924 European ancestry cases, 386,006 European ancestry controls NA Affymetrix, Illumina [510688] 0 meibomian cyst http://www.ebi.ac.uk/efo/EFO_0007363 GCST90079862 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Between 2 and 3 hours (UKB data field 981) (Gene-based burden) 23,530 European ancestry cases, 289,247 European ancestry controls NA Illumina [183664] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083516 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.1: Ectropion of eyelid 581 European ancestry cases, 387,349 European ancestry controls NA Affymetrix, Illumina [510688] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90079869 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration walking for pleasure - Over 3 hours (UKB data field 981) (Gene-based burden) 23,324 European ancestry cases, 289,453 European ancestry controls NA Illumina [183664] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083517 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.0: Age-related incipient cataract 2,535 European ancestry cases, 385,395 European ancestry controls NA Affymetrix, Illumina [510688] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90079885 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Get mildly or occasionally tanned (UKB data field 1727) (Gene-based burden) 93,163 European ancestry cases, 329,407 European ancestry controls NA Illumina [185823] 0 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90081590 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.1: Age-related nuclear cataract 7,306 European ancestry cases, 380,624 European ancestry controls NA Affymetrix, Illumina [510688] 0 Age-related nuclear cataract http://purl.obolibrary.org/obo/HP_0011142 GCST90079886 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Get moderately tanned (UKB data field 1727) (Gene-based burden) 173,164 European ancestry cases, 249,406 European ancestry controls NA Illumina [185823] 0 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90081589 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26.4: Secondary cataract 1,813 European ancestry cases, 386,117 European ancestry controls NA Affymetrix, Illumina [510688] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079890 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Get very tanned (UKB data field 1727) (Gene-based burden) 89,584 European ancestry cases, 332,986 European ancestry controls NA Illumina [185823] 0 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90081588 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26.8: Other specified cataract 787 European ancestry cases, 387,143 European ancestry controls NA Affymetrix, Illumina [510688] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079891 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ease of skin tanning - Never tan only burn (UKB data field 1727) (Gene-based burden) 75,919 European ancestry cases, 346,651 European ancestry controls NA Illumina [185823] 0 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90081591 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33.0: Retinal detachment with retinal break 1,738 European ancestry cases, 386,192 European ancestry controls NA Affymetrix, Illumina [510688] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90079894 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Easily tired during worst period of anxiety (UKB data field 20429) (Gene-based burden) 29,114 European ancestry cases, 11,403 European ancestry controls NA Illumina [135487] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90082432 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35.3: Degeneration of macula and posterior pole 3,347 European ancestry cases, 384,583 European ancestry controls NA Affymetrix, Illumina [510688] 0 degeneration of macula and posterior pole http://purl.obolibrary.org/obo/MONDO_0002175 GCST90079900 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG during exercise duration (UKB data field 6022) (Gene-based burden) 81,703 European ancestry individuals NA Illumina [160268] 0 exercise test http://www.ebi.ac.uk/efo/EFO_0004328 GCST90083398 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H36: Retinal disorders in diseases classified elsewhere 1,750 European ancestry cases, 386,178 European ancestry controls NA Affymetrix, Illumina [510688] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90079904 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ECG heart rate (UKB data field 5983) (Gene-based burden) 80,260 European ancestry individuals NA Illumina [159727] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90083390 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H36.0: Diabetic retinopathy 1,748 European ancestry cases, 386,182 European ancestry controls NA Affymetrix, Illumina [510688] 0 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST90079903 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Education score England (UKB data field 26414) (Gene-based burden) 369,491 European ancestry individuals NA Illumina [185054] 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90082939 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.1: Open-angle glaucoma 1,520 European ancestry cases, 386,410 European ancestry controls NA Affymetrix, Illumina [510688] 0 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90079906 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04: Other nontoxic goiter (Gene-based burden) 2,457 European ancestry cases, 384,010 European ancestry controls NA Illumina [185320] 0 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90083712 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95: Presence of cardiac and vascular implants and grafts 16,113 European ancestry cases, 371,682 European ancestry controls 14,924 European ancestry cases, 34,104 European ancestry controls Affymetrix, Illumina [510575] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081425 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04.1: Nontoxic single thyroid nodule (Gene-based burden) 680 European ancestry cases, 386,990 European ancestry controls NA Illumina [185341] 0 thyroid nodule http://www.ebi.ac.uk/efo/EFO_1001436 GCST90083709 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N35.9: Urethral stricture, unspecified 3,859 European ancestry cases, 383,951 European ancestry controls NA Affymetrix, Illumina [510571] 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90080608 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty concentrating during worst period of anxiety (UKB data field 20419) (Gene-based burden) 31,317 European ancestry cases, 10,080 European ancestry controls NA Illumina [136334] 0 decreased concentration http://purl.obolibrary.org/obo/PATO_0001163 GCST90082424 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.2: Benign lipomatous neoplasm of skin and subcutaneous tissue of limb 1,978 European ancestry cases, 385,952 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90079667 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Fairly difficult (UKB data field 3476) (Gene-based burden) 11,135 European ancestry cases, 19,862 European ancestry controls NA Illumina [126327] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90083044 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.3: Melanocytic nevi of other and unspecified parts of face 1,928 European ancestry cases, 386,001 European ancestry controls NA Affymetrix, Illumina [510688] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90079673 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Fairly easy (UKB data field 3476) (Gene-based burden) 6,721 European ancestry cases, 24,276 European ancestry controls NA Illumina [126327] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90083043 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.5: Melanocytic nevi of trunk 1,702 European ancestry cases, 386,228 European ancestry controls NA Affymetrix, Illumina [510688] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90079674 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Very difficult (UKB data field 3476) (Gene-based burden) 11,547 European ancestry cases, 19,450 European ancestry controls NA Illumina [126327] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90083045 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.6: Melanocytic nevi of upper limb, including shoulder 592 European ancestry cases, 387,338 European ancestry controls NA Affymetrix, Illumina [510688] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90079675 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Very easy (UKB data field 3476) (Gene-based burden) 1,994 European ancestry cases, 29,003 European ancestry controls NA Illumina [126327] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90083042 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.7: Melanocytic nevi of lower limb, including hip 729 European ancestry cases, 387,201 European ancestry controls NA Affymetrix, Illumina [510688] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90079676 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty stopping worrying during worst period of anxiety (UKB data field 20541) (Gene-based burden) 39,704 European ancestry cases, 2,474 European ancestry controls NA Illumina [137068] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082618 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.3: Other benign neoplasm of skin of other and unspecified parts of face 824 European ancestry cases, 387,106 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079679 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Direct bilirubin levels (UKB data field 30660) (Gene-based burden) 351,671 European ancestry individuals NA Illumina [184593] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90083007 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.5: Other benign neoplasm of skin of trunk 765 European ancestry cases, 387,165 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079680 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Discomfort pain occurring only during menstrual bleed (UKB data field 21026) (Gene-based burden) 954 European ancestry cases, 19,437 European ancestry controls NA Illumina [107676] 0 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90082681 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.6: Other benign neoplasm of skin of upper limb, including shoulder 601 European ancestry cases, 387,329 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079681 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - A bit distressing (UKB data field 20462) (Gene-based burden) 1,214 European ancestry cases, 5,497 European ancestry controls NA Illumina [61877] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082485 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.7: Other benign neoplasm of skin of lower limb, including hip 689 European ancestry cases, 387,241 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079682 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Not distressing a neutral experience (UKB data field 20462) (Gene-based burden) 2,103 European ancestry cases, 4,608 European ancestry controls NA Illumina [61877] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082484 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D36.1: Benign neoplasm of peripheral nerves and autonomic nervous system 616 European ancestry cases, 387,313 European ancestry controls 202 European ancestry cases, 102,157 European ancestry controls Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079694 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Distress caused by unusual or psychotic experiences - Not distressing at all it was a positive experience (UKB data field 20462) (Gene-based burden) 1,955 European ancestry cases, 4,756 European ancestry controls NA Illumina [61877] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082483 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R13.1: Dysphagia 843 European ancestry cases, 383,673 European ancestry controls NA Affymetrix, Illumina [507566] 0 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST90080799 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L65: Other nonscarring hair loss (Gene-based burden) 834 European ancestry cases, 384,476 European ancestry controls NA Illumina [185288] 0 alopecia http://purl.obolibrary.org/obo/MONDO_0004907 GCST90084344 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.4: Candidiasis of other urogenital sites 676 European ancestry cases, 383,576 European ancestry controls NA Affymetrix, Illumina [507553] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90079558 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L70: Acne (Gene-based burden) 1,390 European ancestry cases, 382,295 European ancestry controls NA Illumina [185276] 0 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST90084345 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.42: Personal history of other diseases of the female genital tract 837 European ancestry cases, 383,615 European ancestry controls NA Affymetrix, Illumina [507535] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90081372 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L71: Rosacea (Gene-based burden) 4,002 European ancestry cases, 378,283 European ancestry controls NA Illumina [185267] 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90084346 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I80: Phlebitis and thrombophlebitis 6,000 European ancestry cases, 378,260 European ancestry controls NA Affymetrix, Illumina [507531] 0 Phlebitis, Thrombophlebitis http://www.ebi.ac.uk/efo/EFO_1001395, http://purl.obolibrary.org/obo/HP_0004418 GCST90080059 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72: Follicular cysts of skin and subcutaneous tissue (Gene-based burden) 12,083 European ancestry cases, 364,969 European ancestry controls NA Illumina [185187] 0 Follicular Cyst http://www.ebi.ac.uk/efo/EFO_1001329 GCST90084350 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72.9: Follicular cyst of the skin and subcutaneous tissue, unspecified 1,860 European ancestry cases, 382,500 European ancestry controls NA Affymetrix, Illumina [507529] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080363 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72.0: Epidermal cyst (Gene-based burden) 4,196 European ancestry cases, 378,535 European ancestry controls NA Illumina [185287] 0 Epidermal Inclusion Cyst http://www.ebi.ac.uk/efo/EFO_1000243 GCST90084347 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.1: Vomiting 656 European ancestry cases, 383,646 European ancestry controls NA Affymetrix, Illumina [507520] 0 Vomiting http://purl.obolibrary.org/obo/HP_0002013 GCST90080796 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72.1: Pilar and trichodermal cyst (Gene-based burden) 5,572 European ancestry cases, 382,358 European ancestry controls NA Illumina [185344] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084348 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.20: Immunization not carried out because of patient decision for unspecified reason 2,143 European ancestry cases, 382,081 European ancestry controls NA Affymetrix, Illumina [507517] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081224 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72.9: Follicular cyst of the skin and subcutaneous tissue, unspecified (Gene-based burden) 1,860 European ancestry cases, 382,500 European ancestry controls NA Illumina [185307] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084349 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R89.9: Unspecified abnormal finding in specimens from other organs, systems and tissues 2,049 European ancestry cases, 382,289 European ancestry controls NA Affymetrix, Illumina [507514] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080925 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L73: Other follicular disorders (Gene-based burden) 1,494 European ancestry cases, 381,939 European ancestry controls NA Illumina [185277] 0 folliculitis http://www.ebi.ac.uk/efo/EFO_1000702 GCST90084352 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R89.5: Abnormal microbiological findings in specimens from other organs, systems and tissues 831 European ancestry cases, 383,408 European ancestry controls NA Affymetrix, Illumina [507501] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080924 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L73.9: Follicular disorder, unspecified (Gene-based burden) 680 European ancestry cases, 384,976 European ancestry controls NA Illumina [185300] 0 folliculitis http://www.ebi.ac.uk/efo/EFO_1000702 GCST90084351 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.70: Gastritis, unspecified, without bleeding 747 European ancestry cases, 383,610 European ancestry controls NA Affymetrix, Illumina [507475] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90080205 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L81: Other disorders of pigmentation (Gene-based burden) 1,269 European ancestry cases, 384,250 European ancestry controls NA Illumina [185315] 0 pigmentation disease http://www.ebi.ac.uk/efo/EFO_1000755 GCST90084354 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.84: Encounter for antibody response examination 1,714 European ancestry cases, 382,724 European ancestry controls NA Affymetrix, Illumina [507444] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081181 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L81.4: Other melanin hyperpigmentation (Gene-based burden) 629 European ancestry cases, 387,299 European ancestry controls NA Illumina [185344] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084353 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Liverfc 2,899 European ancestry cases, 381,358 European ancestry controls NA Affymetrix, Illumina [507444] 1 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90081531 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L82: Seborrheic keratosis (Gene-based burden) 10,168 European ancestry cases, 361,048 European ancestry controls NA Illumina [185052] 0 seborrheic keratosis http://www.ebi.ac.uk/efo/EFO_0005584 GCST90084355 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R59: Enlarged lymph nodes 3,668 European ancestry cases, 380,619 European ancestry controls NA Affymetrix, Illumina [507436] 0 Lymphadenopathy http://purl.obolibrary.org/obo/HP_0002716 GCST90080887 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L30: Other and unspecified dermatitis (Gene-based burden) 11,384 European ancestry cases, 355,935 European ancestry controls NA Illumina [185015] 0 dermatitis http://purl.obolibrary.org/obo/MONDO_0002406 GCST90084332 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40: Glaucoma 8,122 European ancestry cases, 376,438 European ancestry controls 8,012 European ancestry cases, 113,883 European ancestry controls Affymetrix, Illumina [507698] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90079909 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L30.9: Dermatitis, unspecified (Gene-based burden) 1,998 European ancestry cases, 385,119 European ancestry controls NA Illumina [185334] 0 dermatitis http://purl.obolibrary.org/obo/MONDO_0002406 GCST90084331 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R32: Unspecified urinary incontinence 4,119 European ancestry cases, 380,440 European ancestry controls NA Affymetrix, Illumina [507689] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90080843 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40: Psoriasis (Gene-based burden) 5,629 European ancestry cases, 377,623 European ancestry controls NA Illumina [185263] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90084335 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H65: Nonsuppurative otitis media 1,877 European ancestry cases, 382,674 European ancestry controls NA Affymetrix, Illumina [507683] 0 otitis media with effusion http://www.ebi.ac.uk/efo/EFO_0007415 GCST90079932 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40.5: Arthropathic psoriasis (Gene-based burden) 1,104 European ancestry cases, 386,481 European ancestry controls NA Illumina [185338] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90084333 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.81: Other malaise 670 European ancestry cases, 383,920 European ancestry controls NA Affymetrix, Illumina [507658] 0 malaise http://www.ebi.ac.uk/efo/EFO_0009641 GCST90080874 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40.9: Psoriasis, unspecified (Gene-based burden) 2,364 European ancestry cases, 384,617 European ancestry controls NA Illumina [185319] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90084334 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26: Other cataract 20,291 European ancestry cases, 364,151 European ancestry controls 10,824 European ancestry cases, 103,681 European ancestry controls Affymetrix, Illumina [507653] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079893 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L43: Lichen planus (Gene-based burden) 1,295 European ancestry cases, 385,047 European ancestry controls NA Illumina [185306] 0 lichen planus http://www.ebi.ac.uk/efo/EFO_1000726 GCST90084337 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35: Other retinal disorders 5,808 European ancestry cases, 378,620 European ancestry controls 7,142 European ancestry cases, 112,683 European ancestry controls Affymetrix, Illumina [507646] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90079902 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L43.9: Lichen planus, unspecified (Gene-based burden) 612 European ancestry cases, 387,316 European ancestry controls NA Illumina [185344] 0 lichen planus http://www.ebi.ac.uk/efo/EFO_1000726 GCST90084336 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R49.8: Other voice and resonance disorders 1,104 European ancestry cases, 383,346 European ancestry controls NA Affymetrix, Illumina [507640] 0 voice disorders http://www.ebi.ac.uk/efo/EFO_0009692 GCST90080866 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L50: Urticaria (Gene-based burden) 2,279 European ancestry cases, 378,852 European ancestry controls NA Illumina [185228] 0 urticaria http://www.ebi.ac.uk/efo/EFO_0005531 GCST90084338 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.1: Other difficulties with micturition 2,813 European ancestry cases, 381,615 European ancestry controls NA Affymetrix, Illumina [507626] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90080849 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L53.9: Erythematous condition, unspecified (Gene-based burden) 647 European ancestry cases, 386,732 European ancestry controls NA Illumina [185336] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084339 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R13.10: Dysphagia, unspecified 840 European ancestry cases, 383,714 European ancestry controls NA Affymetrix, Illumina [507606] 0 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST90080798 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L57: Skin changes due to chronic exposure to nonionizing radiation (Gene-based burden) 7,797 European ancestry cases, 370,171 European ancestry controls NA Illumina [185185] 0 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90084341 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K04: Diseases of pulp and periapical tissues 3,161 European ancestry cases, 381,325 European ancestry controls NA Affymetrix, Illumina [507592] 0 dental pulp disease http://www.ebi.ac.uk/efo/EFO_0009540 GCST90080168 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L57.0: Actinic keratosis (Gene-based burden) 3,010 European ancestry cases, 384,062 European ancestry controls NA Illumina [185337] 0 actinic keratosis http://www.ebi.ac.uk/efo/EFO_0002496 GCST90084340 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L29.9: Pruritus, unspecified 1,139 European ancestry cases, 383,369 European ancestry controls NA Affymetrix, Illumina [507588] 0 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST90080343 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L60: Nail disorders (Gene-based burden) 3,890 European ancestry cases, 374,676 European ancestry controls NA Illumina [185210] 0 nail anomaly http://purl.obolibrary.org/obo/MONDO_0019283 GCST90084343 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J31.0: Chronic rhinitis 1,949 European ancestry cases, 382,383 European ancestry controls NA Affymetrix, Illumina [507577] 0 rhinitis http://www.ebi.ac.uk/efo/EFO_0008521 GCST90080105 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L60.0: Ingrowing nail (Gene-based burden) 928 European ancestry cases, 387,002 European ancestry controls NA Illumina [185344] 0 nail anomaly http://purl.obolibrary.org/obo/MONDO_0019283 GCST90084342 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z04.8: Encounter for examination and observation for other specified reasons 923 European ancestry cases, 387,005 European ancestry controls NA Affymetrix, Illumina [510687] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081195 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - Not at all (UKB data field 2070) (Gene-based burden) 311,760 European ancestry cases, 103,751 European ancestry controls NA Illumina [185718] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082661 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.8: Care involving use of other rehabilitation procedures 669 European ancestry cases, 387,261 European ancestry controls NA Affymetrix, Illumina [510687] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081275 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - Several days (UKB data field 2070) (Gene-based burden) 96,739 European ancestry cases, 318,772 European ancestry controls NA Illumina [185718] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082662 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.2: Acquired absence of lung [part of] 757 European ancestry cases, 387,171 European ancestry controls NA Affymetrix, Illumina [510687] 0 lung transplantation http://www.ebi.ac.uk/efo/EFO_0010721 GCST90081391 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - More than half the days (UKB data field 2080) (Gene-based burden) 26,703 European ancestry cases, 392,133 European ancestry controls NA Illumina [185780] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90082667 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.2: Presence of prosthetic heart valve 1,244 European ancestry cases, 386,684 European ancestry controls NA Affymetrix, Illumina [510687] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081421 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - Nearly every day (UKB data field 2080) (Gene-based burden) 27,214 European ancestry cases, 391,622 European ancestry controls NA Illumina [185780] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90082668 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.0: Intestinal bypass and anastomosis status 2,891 European ancestry cases, 385,037 European ancestry controls 775 European ancestry cases, 31,530 European ancestry controls Affymetrix, Illumina [510687] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081435 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - Not at all (UKB data field 2080) (Gene-based burden) 204,460 European ancestry cases, 214,376 European ancestry controls NA Illumina [185780] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082665 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.5: Pseudomonas (aeruginosa) (mallei) (pseudomallei) as the cause of diseases classified elsewhere 1,140 European ancestry cases, 386,786 European ancestry controls NA Affymetrix, Illumina [510686] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079567 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tiredness lethargy in last 2 weeks - Several days (UKB data field 2080) (Gene-based burden) 180,228 European ancestry cases, 238,608 European ancestry controls NA Illumina [185780] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90082666 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34.9: Malignant neoplasm of unspecified part of bronchus or lung 2,548 European ancestry cases, 385,381 European ancestry controls NA Affymetrix, Illumina [510686] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90079589 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - More than half the days (UKB data field 2060) (Gene-based burden) 11,544 European ancestry cases, 405,923 European ancestry controls NA Illumina [185726] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082659 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.5: Other and unspecified malignant neoplasm of skin of trunk 2,526 European ancestry cases, 385,397 European ancestry controls NA Affymetrix, Illumina [510686] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079598 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - Nearly every day (UKB data field 2060) (Gene-based burden) 8,385 European ancestry cases, 409,082 European ancestry controls NA Illumina [185726] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082660 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.6: Other and unspecified malignant neoplasm of skin of upper limb, including shoulder 1,542 European ancestry cases, 386,385 European ancestry controls NA Affymetrix, Illumina [510686] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079599 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - Not at all (UKB data field 2060) (Gene-based burden) 335,869 European ancestry cases, 81,598 European ancestry controls NA Illumina [185726] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082657 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G45.9: Transient cerebral ischemic attack, unspecified 2,495 European ancestry cases, 385,423 European ancestry controls NA Affymetrix, Illumina [510686] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90079829 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - Several days (UKB data field 2060) (Gene-based burden) 71,590 European ancestry cases, 345,877 European ancestry controls NA Illumina [185726] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082658 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.9: Unspecified age-related cataract 1,887 European ancestry cases, 386,041 European ancestry controls NA Affymetrix, Illumina [510686] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90079888 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unusual or psychotic experiences in past year - Not at all (UKB data field 20467) (Gene-based burden) 4,948 European ancestry cases, 1,913 European ancestry controls NA Illumina [62672] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082490 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I24.9: Acute ischemic heart disease, unspecified 1,039 European ancestry cases, 386,891 European ancestry controls NA Affymetrix, Illumina [510686] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90079976 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unusual or psychotic experiences in past year - Once or twice (UKB data field 20467) (Gene-based burden) 1,216 European ancestry cases, 5,645 European ancestry controls NA Illumina [62672] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90082491 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.1: Atrioventricular block, second degree 650 European ancestry cases, 387,280 European ancestry controls NA Affymetrix, Illumina [510686] 0 Second degree atrioventricular block http://purl.obolibrary.org/obo/HP_0011706 GCST90080002 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L84: Corns and callosities (Gene-based burden) 706 European ancestry cases, 384,517 European ancestry controls NA Illumina [185290] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084356 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A09: Infectious gastroenteritis and colitis, unspecified 9,743 European ancestry cases, 374,480 European ancestry controls NA Affymetrix, Illumina [507421] 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90079543 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L85: Other epidermal thickening (Gene-based burden) 2,073 European ancestry cases, 378,173 European ancestry controls NA Illumina [185226] 0 Epidermal thickening http://purl.obolibrary.org/obo/HP_0011368 GCST90084358 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44: Other and unspecified malignant neoplasm of skin 15,858 European ancestry cases, 368,260 European ancestry controls NA Affymetrix, Illumina [507410] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079601 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R04.2: Hemoptysis (Gene-based burden) 2,545 European ancestry cases, 384,924 European ancestry controls NA Illumina [185343] 0 Hemoptysis http://purl.obolibrary.org/obo/HP_0002105 GCST90084748 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.89: Other specified postprocedural states 10,483 European ancestry cases, 355,404 European ancestry controls NA Affymetrix, Illumina [491137] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081438 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R05: Cough (Gene-based burden) 19,858 European ancestry cases, 346,074 European ancestry controls NA Illumina [184998] 0 Cough http://purl.obolibrary.org/obo/HP_0012735 GCST90084750 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R05: Cough 19,858 European ancestry cases, 346,074 European ancestry controls NA Affymetrix, Illumina [490976] 0 Cough http://purl.obolibrary.org/obo/HP_0012735 GCST90080764 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06: Abnormalities of breathing (Gene-based burden) 20,491 European ancestry cases, 352,838 European ancestry controls NA Illumina [185079] 0 irregular respiration http://www.ebi.ac.uk/efo/EFO_0009841 GCST90084758 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R21: Rash and other nonspecific skin eruption 13,788 European ancestry cases, 351,645 European ancestry controls NA Affymetrix, Illumina [490673] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080818 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.0: Dyspnea (Gene-based burden) 15,391 European ancestry cases, 362,721 European ancestry controls NA Illumina [185165] 0 Dyspnea http://purl.obolibrary.org/obo/HP_0002094 GCST90084753 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00: Abnormalities of heart beat 30,622 European ancestry cases, 334,318 European ancestry controls NA Affymetrix, Illumina [490301] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90080754 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.00: Dyspnea, unspecified (Gene-based burden) 4,013 European ancestry cases, 375,874 European ancestry controls NA Illumina [185211] 0 Dyspnea http://purl.obolibrary.org/obo/HP_0002094 GCST90084751 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98: Other postprocedural states 15,101 European ancestry cases, 349,629 European ancestry controls NA Affymetrix, Illumina [490089] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081440 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.09: Other forms of dyspnea (Gene-based burden) 4,927 European ancestry cases, 378,978 European ancestry controls NA Illumina [185269] 0 Dyspnea http://purl.obolibrary.org/obo/HP_0002094 GCST90084752 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.5: Low back pain 22,734 European ancestry cases, 341,460 European ancestry controls NA Affymetrix, Illumina [489276] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90080510 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.2: Wheezing (Gene-based burden) 1,393 European ancestry cases, 383,622 European ancestry controls NA Illumina [185300] 0 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90084754 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53: Persons encountering health services for specific procedures and treatment, not carried out 42,753 European ancestry cases, 320,965 European ancestry controls NA Affymetrix, Illumina [489252] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081292 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.5: Mouth breathing (Gene-based burden) 2,287 European ancestry cases, 385,623 European ancestry controls NA Illumina [185344] 0 Abnormal pattern of respiration http://purl.obolibrary.org/obo/HP_0002793 GCST90084755 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inflammatory bowel disease - loose composite 5,509 European ancestry cases, 358,527 European ancestry controls NA Affymetrix, Illumina [489186] 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90081487 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I12: Hypertensive chronic kidney disease (Gene-based burden) 1,660 European ancestry cases, 386,252 European ancestry controls NA Illumina [185344] 0 hypertensive nephropathy http://purl.obolibrary.org/obo/MONDO_0024633 GCST90083950 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R33: Retention of urine 9,413 European ancestry cases, 377,878 European ancestry controls NA Affymetrix, Illumina [510128] 0 Urinary retention http://purl.obolibrary.org/obo/HP_0000016 GCST90080844 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I12.0: Hypertensive chronic kidney disease with stage 5 chronic kidney disease or end stage renal disease (Gene-based burden) 1,504 European ancestry cases, 386,426 European ancestry controls NA Illumina [185344] 0 hypertensive nephropathy http://purl.obolibrary.org/obo/MONDO_0024633 GCST90083949 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R47: Speech disturbances, not elsewhere classified 2,139 European ancestry cases, 385,206 European ancestry controls NA Affymetrix, Illumina [510128] 0 Speech apraxia http://purl.obolibrary.org/obo/HP_0011098 GCST90080864 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20: Angina pectoris (Gene-based burden) 22,332 European ancestry cases, 364,233 European ancestry controls NA Illumina [185323] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90083954 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 504 Always (UKB data field 21034) (Gene-based burden) 1,097 European ancestry cases, 153,989 European ancestry controls NA Illumina [174051] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082717 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K25.9: Gastric ulcer, unspecified as acute or chronic, without hemorrhage or perforation 4,625 European ancestry cases, 383,304 European ancestry controls NA Affymetrix, Illumina [510687] 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90080196 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Less than monthly (UKB data field 20408) (Gene-based burden) 8,452 European ancestry cases, 68,159 European ancestry controls NA Illumina [156101] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082396 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.7: Ileus, unspecified 590 European ancestry cases, 387,340 European ancestry controls NA Affymetrix, Illumina [510687] 0 ileus http://purl.obolibrary.org/obo/MONDO_0004567 GCST90080243 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Monthly (UKB data field 20408) (Gene-based burden) 1,315 European ancestry cases, 75,296 European ancestry controls NA Illumina [156101] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082397 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K65.0: Generalized (acute) peritonitis 598 European ancestry cases, 387,332 European ancestry controls NA Affymetrix, Illumina [510687] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90080278 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Never (UKB data field 20408) (Gene-based burden) 66,108 European ancestry cases, 10,503 European ancestry controls NA Illumina [156101] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082395 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83.1: Obstruction of bile duct 1,070 European ancestry cases, 386,859 European ancestry controls NA Affymetrix, Illumina [510687] 0 cholestasis http://purl.obolibrary.org/obo/MONDO_0001751 GCST90080306 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Weekly (UKB data field 20408) (Gene-based burden) 608 European ancestry cases, 76,003 European ancestry controls NA Illumina [156101] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082398 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K90.0: Celiac disease 2,213 European ancestry cases, 385,716 European ancestry controls 813 European ancestry cases, 111,270 European ancestry controls Affymetrix, Illumina [510687] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90080314 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 11 to 15 times a day (UKB data field 943) (Gene-based burden) 87,890 European ancestry cases, 339,312 European ancestry controls NA Illumina [185892] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083501 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L43.9: Lichen planus, unspecified 612 European ancestry cases, 387,316 European ancestry controls NA Affymetrix, Illumina [510687] 0 lichen planus http://www.ebi.ac.uk/efo/EFO_1000726 GCST90080350 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 16 to 20 times a day (UKB data field 943) (Gene-based burden) 41,655 European ancestry cases, 385,547 European ancestry controls NA Illumina [185892] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083502 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L81.4: Other melanin hyperpigmentation 629 European ancestry cases, 387,299 European ancestry controls NA Affymetrix, Illumina [510687] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080367 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - More than 20 times a day (UKB data field 943) (Gene-based burden) 31,850 European ancestry cases, 395,352 European ancestry controls NA Illumina [185892] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083503 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10.99: Gout, unspecified 1,845 European ancestry cases, 386,085 European ancestry controls NA Affymetrix, Illumina [510687] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90080394 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - None (UKB data field 943) (Gene-based burden) 40,865 European ancestry cases, 386,337 European ancestry controls NA Illumina [185892] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083498 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M24.16: Other articular cartilage disorders 605 European ancestry cases, 387,325 European ancestry controls NA Affymetrix, Illumina [510687] 0 articular cartilage of joint http://purl.obolibrary.org/obo/UBERON_0010996 GCST90080448 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 1 to 5 times a day (UKB data field 943) (Gene-based burden) 89,153 European ancestry cases, 338,049 European ancestry controls NA Illumina [185892] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083499 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N31.9: Neuromuscular dysfunction of bladder, unspecified 816 European ancestry cases, 387,114 European ancestry controls NA Affymetrix, Illumina [510687] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90080601 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of stair climbing in last 4 weeks - 6 to 10 times a day (UKB data field 943) (Gene-based burden) 165,029 European ancestry cases, 262,173 European ancestry controls NA Illumina [185892] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083500 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.8: Other specified place 998 European ancestry cases, 386,932 European ancestry controls NA Affymetrix, Illumina [510687] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081103 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - More than half the days (UKB data field 2070) (Gene-based burden) 11,135 European ancestry cases, 404,376 European ancestry controls NA Illumina [185718] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082663 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W44: Foreign body entering into or through eye or natural orifice causing accidental injury 690 European ancestry cases, 387,240 European ancestry controls NA Affymetrix, Illumina [510687] 0 eye foreign body http://www.ebi.ac.uk/efo/EFO_1001322 GCST90081128 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - Nearly every day (UKB data field 2070) (Gene-based burden) 7,849 European ancestry cases, 407,662 European ancestry controls NA Illumina [185718] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082664 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - Every day (UKB data field 971) (Gene-based burden) 40,526 European ancestry cases, 272,358 European ancestry controls NA Illumina [183670] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083510 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40.2: Bilateral inguinal hernia, without obstruction or gangrene 1,780 European ancestry cases, 386,150 European ancestry controls NA Affymetrix, Illumina [510686] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90080218 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.8: Other abdominal pain 604 European ancestry cases, 384,099 European ancestry controls NA Affymetrix, Illumina [507820] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90080790 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08.8: Other specified local infections of the skin and subcutaneous tissue (Gene-based burden) 973 European ancestry cases, 384,549 European ancestry controls NA Illumina [185301] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084320 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R44: Other symptoms and signs involving general sensations and perceptions 1,374 European ancestry cases, 383,396 European ancestry controls NA Affymetrix, Illumina [507818] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90080859 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08.89: Other specified local infections of the skin and subcutaneous tissue (Gene-based burden) 716 European ancestry cases, 385,049 European ancestry controls NA Illumina [185305] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084319 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.57: Pain in ankle and joints of foot 1,961 European ancestry cases, 382,634 European ancestry controls NA Affymetrix, Illumina [507815] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90080459 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08.9: Local infection of the skin and subcutaneous tissue, unspecified (Gene-based burden) 3,110 European ancestry cases, 376,282 European ancestry controls NA Illumina [185186] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084321 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L01: Impetigo 591 European ancestry cases, 384,013 European ancestry controls NA Affymetrix, Illumina [507810] 0 impetigo http://www.ebi.ac.uk/efo/EFO_1000714 GCST90080323 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L20: Atopic dermatitis (Gene-based burden) 2,972 European ancestry cases, 375,981 European ancestry controls NA Illumina [185204] 0 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90084323 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.898.: Other symptoms and signs involving the musculoskeletal system 585 European ancestry cases, 384,066 European ancestry controls NA Affymetrix, Illumina [507800] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90080833 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L21: Seborrheic dermatitis (Gene-based burden) 2,156 European ancestry cases, 379,083 European ancestry controls NA Illumina [185248] 0 seborrheic dermatitis http://www.ebi.ac.uk/efo/EFO_1000764 GCST90084324 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.89: Other symptoms and signs involving the musculoskeletal system 585 European ancestry cases, 384,062 European ancestry controls NA Affymetrix, Illumina [507797] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90080834 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L25: Unspecified contact dermatitis (Gene-based burden) 799 European ancestry cases, 382,796 European ancestry controls NA Illumina [185290] 0 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90084325 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.50: Pain in unspecified joint 1,272 European ancestry cases, 383,393 European ancestry controls NA Affymetrix, Illumina [507777] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90080453 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L27: Dermatitis due to substances taken internally (Gene-based burden) 633 European ancestry cases, 387,042 European ancestry controls NA Illumina [185329] 0 dermatitis http://purl.obolibrary.org/obo/MONDO_0002406 GCST90084327 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.4: Encounter for surveillance of contraceptives 1,670 European ancestry cases, 382,887 European ancestry controls NA Affymetrix, Illumina [507750] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081238 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L27.0: Generalized skin eruption due to drugs and medicaments taken internally (Gene-based burden) 514 European ancestry cases, 387,400 European ancestry controls NA Illumina [185344] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084326 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G44: Other headache syndromes 1,382 European ancestry cases, 383,155 European ancestry controls NA Affymetrix, Illumina [507737] 0 headache disorder http://www.ebi.ac.uk/efo/EFO_0009550 GCST90079828 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L29: Pruritus (Gene-based burden) 5,379 European ancestry cases, 369,164 European ancestry controls NA Illumina [185136] 0 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST90084330 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.0: Nausea 827 European ancestry cases, 383,789 European ancestry controls NA Affymetrix, Illumina [507723] 0 Nausea http://purl.obolibrary.org/obo/HP_0002018 GCST90080793 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L29.0: Pruritus ani (Gene-based burden) 1,392 European ancestry cases, 383,825 European ancestry controls NA Illumina [185309] 0 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST90084328 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R35.1: Nocturia 931 European ancestry cases, 383,625 European ancestry controls NA Affymetrix, Illumina [507721] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90080846 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L29.9: Pruritus, unspecified (Gene-based burden) 1,139 European ancestry cases, 383,369 European ancestry controls NA Illumina [185295] 0 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST90084329 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.5: Hemorrhage of anus and rectum 15,430 European ancestry cases, 369,154 European ancestry controls NA Affymetrix, Illumina [507708] 0 Gastrointestinal hemorrhage http://purl.obolibrary.org/obo/HP_0002239 GCST90080265 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H57: Other disorders of eye and adnexa (Gene-based burden) 4,926 European ancestry cases, 365,834 European ancestry controls NA Illumina [185056] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083912 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.0: Encounter for screening for diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism 3,572 European ancestry cases, 383,893 European ancestry controls NA Affymetrix, Illumina [510252] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081212 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H57.9: Unspecified disorder of eye and adnexa (Gene-based burden) 3,361 European ancestry cases, 372,277 European ancestry controls NA Illumina [185131] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083911 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00.0: Superficial injury of scalp 537 European ancestry cases, 386,906 European ancestry controls NA Affymetrix, Illumina [510251] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080938 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H60: Otitis externa (Gene-based burden) 10,706 European ancestry cases, 361,578 European ancestry controls NA Illumina [185079] 0 otitis externa http://www.ebi.ac.uk/efo/EFO_0009560 GCST90083915 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.34: Trigger finger, ring finger 1,114 European ancestry cases, 386,816 European ancestry controls NA Affymetrix, Illumina [510688] 0 stenosing tenosynovitis http://www.ebi.ac.uk/efo/EFO_0010822 GCST90080516 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 6 (UKB data field 4968) (Gene-based burden) 146,554 European ancestry cases, 10,399 European ancestry controls NA Illumina [174673] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083226 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.96: Synovitis and tenosynovitis, unspecified 944 European ancestry cases, 386,986 European ancestry controls NA Affymetrix, Illumina [510688] 0 pigmented villonodular synovitis http://www.ebi.ac.uk/efo/EFO_1001106 GCST90080518 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 7 (UKB data field 20171) (Gene-based burden) 781 European ancestry cases, 108,156 European ancestry controls NA Illumina [166662] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082323 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M67.8: Other specified disorders of synovium and tendon 697 European ancestry cases, 387,233 European ancestry controls NA Affymetrix, Illumina [510688] 0 synovium disorder http://purl.obolibrary.org/obo/MONDO_0056799 GCST90080523 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 7 (UKB data field 4968) (Gene-based burden) 1,224 European ancestry cases, 155,729 European ancestry controls NA Illumina [174673] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083227 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M70.6: Trochanteric bursitis 904 European ancestry cases, 387,026 European ancestry controls NA Affymetrix, Illumina [510688] 0 bursitis http://purl.obolibrary.org/obo/MONDO_0002471 GCST90080525 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 8 (UKB data field 20171) (Gene-based burden) 1,587 European ancestry cases, 107,350 European ancestry controls NA Illumina [166662] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082324 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M71.2: Synovial cyst of popliteal space [Baker] 560 European ancestry cases, 387,370 European ancestry controls NA Affymetrix, Illumina [510688] 0 synovium disorder http://purl.obolibrary.org/obo/MONDO_0056799 GCST90080527 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 8 (UKB data field 4968) (Gene-based burden) 2,396 European ancestry cases, 154,557 European ancestry controls NA Illumina [174673] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083228 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M72.0: Palmar fascial fibromatosis [Dupuytren] 4,263 European ancestry cases, 383,667 European ancestry controls NA Affymetrix, Illumina [510688] 0 Palmar Fibromatosis http://www.ebi.ac.uk/efo/EFO_1000438 GCST90080530 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 9 (UKB data field 20171) (Gene-based burden) 3,716 European ancestry cases, 105,221 European ancestry controls NA Illumina [166662] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082325 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.0: Adhesive capsulitis of shoulder 1,966 European ancestry cases, 385,964 European ancestry controls NA Affymetrix, Illumina [510688] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080532 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - aunt (UKB data field 20173) (Gene-based burden) 10,201 European ancestry cases, 96,638 European ancestry controls NA Illumina [166122] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082326 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.4: Impingement syndrome of shoulder 6,024 European ancestry cases, 381,906 European ancestry controls NA Affymetrix, Illumina [510688] 0 shoulder impingement syndrome http://www.ebi.ac.uk/efo/EFO_1001178 GCST90080534 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - aunt (UKB data field 4979) (Gene-based burden) 17,526 European ancestry cases, 121,844 European ancestry controls NA Illumina [172330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083229 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.5: Bursitis of shoulder 895 European ancestry cases, 387,035 European ancestry controls NA Affymetrix, Illumina [510688] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080535 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - cousin (UKB data field 20173) (Gene-based burden) 59,485 European ancestry cases, 47,354 European ancestry controls NA Illumina [166122] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082329 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M77.1: Lateral epicondylitis 768 European ancestry cases, 387,162 European ancestry controls NA Affymetrix, Illumina [510688] 0 lateral epicondylitis http://www.ebi.ac.uk/efo/EFO_1001896 GCST90080539 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - cousin (UKB data field 4979) (Gene-based burden) 86,002 European ancestry cases, 53,368 European ancestry controls NA Illumina [172330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083232 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.09: Rheumatism, unspecified 657 European ancestry cases, 387,273 European ancestry controls NA Affymetrix, Illumina [510688] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90080542 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - niece (UKB data field 20173) (Gene-based burden) 12,210 European ancestry cases, 94,629 European ancestry controls NA Illumina [166122] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082328 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.65: Pain in thigh 909 European ancestry cases, 387,021 European ancestry controls NA Affymetrix, Illumina [510688] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90080546 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - niece (UKB data field 4979) (Gene-based burden) 21,550 European ancestry cases, 117,820 European ancestry controls NA Illumina [172330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083231 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.66: Pain in lower leg 3,465 European ancestry cases, 384,465 European ancestry controls NA Affymetrix, Illumina [510688] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90080547 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - no relation (UKB data field 20173) (Gene-based burden) 14,557 European ancestry cases, 92,282 European ancestry controls NA Illumina [166122] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082330 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.7: Fibromyalgia 1,545 European ancestry cases, 386,385 European ancestry controls NA Affymetrix, Illumina [510688] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90080551 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - no relation (UKB data field 4979) (Gene-based burden) 8,036 European ancestry cases, 131,334 European ancestry controls NA Illumina [172330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083233 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.79: Fibromyalgia 539 European ancestry cases, 387,391 European ancestry controls NA Affymetrix, Illumina [510688] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90080550 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - sister (UKB data field 20173) (Gene-based burden) 10,386 European ancestry cases, 96,453 European ancestry controls NA Illumina [166122] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082327 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.86: Other specified soft tissue disorders 3,840 European ancestry cases, 384,090 European ancestry controls NA Affymetrix, Illumina [510688] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080552 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI5 family relationship calculation - sister (UKB data field 4979) (Gene-based burden) 13,858 European ancestry cases, 125,512 European ancestry controls NA Illumina [172330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083230 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M80.9: Unspecified osteoporosis with pathological fracture 815 European ancestry cases, 387,115 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90080555 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 68 (UKB data field 20175) (Gene-based burden) 646 European ancestry cases, 95,556 European ancestry controls NA Illumina [163252] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082331 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81.9: Osteoporosis, unspecified 8,206 European ancestry cases, 379,724 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90080558 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 69 (UKB data field 20175) (Gene-based burden) 72,471 European ancestry cases, 23,731 European ancestry controls NA Illumina [163252] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082332 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81.99: Osteoporosis, unspecified 3,895 European ancestry cases, 384,035 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90080557 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 70 (UKB data field 20175) (Gene-based burden) 20,903 European ancestry cases, 75,299 European ancestry controls NA Illumina [163252] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082333 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M84.1: Nonunion of fracture [pseudarthrosis] 1,026 European ancestry cases, 386,904 European ancestry controls NA Affymetrix, Illumina [510688] 0 fractures, ununited http://www.ebi.ac.uk/efo/EFO_0009707 GCST90080560 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 71 (UKB data field 20175) (Gene-based burden) 1,122 European ancestry cases, 95,080 European ancestry controls NA Illumina [163252] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082334 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13.2: Hydronephrosis with renal and ureteral calculous obstruction 892 European ancestry cases, 387,038 European ancestry controls NA Affymetrix, Illumina [510688] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90080575 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 72 (UKB data field 20175) (Gene-based burden) 1,060 European ancestry cases, 95,142 European ancestry controls NA Illumina [163252] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082335 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13.3: Other and unspecified hydronephrosis 1,654 European ancestry cases, 386,276 European ancestry controls NA Affymetrix, Illumina [510688] 0 hydronephrosis http://www.ebi.ac.uk/efo/EFO_0005562 GCST90080576 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 68 (UKB data field 4990) (Gene-based burden) 723 European ancestry cases, 135,668 European ancestry controls NA Illumina [171491] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083234 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13.5: Crossing vessel and stricture of ureter without hydronephrosis 597 European ancestry cases, 387,333 European ancestry controls NA Affymetrix, Illumina [510688] 0 stricture or kinking of ureter http://purl.obolibrary.org/obo/MONDO_0002674 GCST90080577 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 69 (UKB data field 4990) (Gene-based burden) 106,949 European ancestry cases, 29,442 European ancestry controls NA Illumina [171491] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083235 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18.3: Chronic kidney disease, stage 3 (moderate) 3,948 European ancestry cases, 383,982 European ancestry controls NA Affymetrix, Illumina [510688] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90080581 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 70 (UKB data field 4990) (Gene-based burden) 31,252 European ancestry cases, 105,139 European ancestry controls NA Illumina [171491] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083236 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18.4: Chronic kidney disease, stage 4 (severe) 545 European ancestry cases, 387,385 European ancestry controls NA Affymetrix, Illumina [510688] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90080582 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 71 (UKB data field 4990) (Gene-based burden) 739 European ancestry cases, 135,652 European ancestry controls NA Illumina [171491] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083237 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18.9: Chronic kidney disease, unspecified 3,916 European ancestry cases, 384,014 European ancestry controls 5,101 European ancestry cases, 99,375 European ancestry controls Affymetrix, Illumina [510688] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90080583 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI6 conditional arithmetic - 72 (UKB data field 4990) (Gene-based burden) 885 European ancestry cases, 135,506 European ancestry controls NA Illumina [171491] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083238 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N31.8: Other neuromuscular dysfunction of bladder 866 European ancestry cases, 387,064 European ancestry controls NA Affymetrix, Illumina [510688] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90080600 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - break (UKB data field 5001) (Gene-based burden) 1,234 European ancestry cases, 125,748 European ancestry controls NA Illumina [170038] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083244 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.3: Diverticulum of bladder 1,020 European ancestry cases, 386,910 European ancestry controls NA Affymetrix, Illumina [510688] 0 bladder diverticulum http://purl.obolibrary.org/obo/MONDO_0007197 GCST90080604 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - cease (UKB data field 20177) (Gene-based burden) 73,454 European ancestry cases, 5,148 European ancestry controls NA Illumina [157134] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082338 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R02: Gangrene, not elsewhere classified 821 European ancestry cases, 387,109 European ancestry controls NA Affymetrix, Illumina [510688] 0 gangrene http://www.ebi.ac.uk/efo/EFO_0008574 GCST90080757 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - cease (UKB data field 5001) (Gene-based burden) 112,537 European ancestry cases, 14,445 European ancestry controls NA Illumina [170038] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083243 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.3: Other chest pain 10,838 European ancestry cases, 377,092 European ancestry controls NA Affymetrix, Illumina [510688] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90080774 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - close (UKB data field 20177) (Gene-based burden) 720 European ancestry cases, 77,882 European ancestry controls NA Illumina [157134] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082337 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.4: Chest pain, unspecified 26,118 European ancestry cases, 361,812 European ancestry controls NA Affymetrix, Illumina [510688] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90080775 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - close (UKB data field 5001) (Gene-based burden) 2,049 European ancestry cases, 124,933 European ancestry controls NA Illumina [170038] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083242 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.4: Other and unspecified abdominal pain 20,448 European ancestry cases, 367,482 European ancestry controls NA Affymetrix, Illumina [510688] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90080789 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - pause (UKB data field 20177) (Gene-based burden) 3,504 European ancestry cases, 75,098 European ancestry controls NA Illumina [157134] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082336 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R52.1: Chronic intractable pain 868 European ancestry cases, 387,062 European ancestry controls NA Affymetrix, Illumina [510688] 0 Chronic pain http://purl.obolibrary.org/obo/HP_0012532 GCST90080871 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - pause (UKB data field 5001) (Gene-based burden) 11,287 European ancestry cases, 115,695 European ancestry controls NA Illumina [170038] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083241 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R52.2: Other chronic pain 509 European ancestry cases, 387,421 European ancestry controls NA Affymetrix, Illumina [510688] 0 Chronic pain http://purl.obolibrary.org/obo/HP_0012532 GCST90080872 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - rest (UKB data field 5001) (Gene-based burden) 1,461 European ancestry cases, 125,521 European ancestry controls NA Illumina [170038] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083245 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 503 Most of the time (UKB data field 21034) (Gene-based burden) 6,888 European ancestry cases, 148,198 European ancestry controls NA Illumina [174051] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082716 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J96.0: Acute respiratory failure 503 European ancestry cases, 387,427 European ancestry controls NA Affymetrix, Illumina [510687] 0 acute respiratory failure http://purl.obolibrary.org/obo/MONDO_0001208 GCST90080155 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F52: Sexual dysfunction not due to a substance or known physiological condition 682 European ancestry cases, 385,926 European ancestry controls NA Affymetrix, Illumina [509497] 0 physiological sexual disorder http://purl.obolibrary.org/obo/MONDO_0002134 GCST90079815 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34.2: Deviated nasal septum (Gene-based burden) 4,524 European ancestry cases, 382,965 European ancestry controls NA Illumina [185333] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084100 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.1: Personal history of diseases of the digestive system 20,497 European ancestry cases, 366,069 European ancestry controls 3,373 European ancestry cases, 30,055 European ancestry controls Affymetrix, Illumina [509497] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90081368 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34.3: Hypertrophy of nasal turbinates (Gene-based burden) 1,949 European ancestry cases, 385,981 European ancestry controls NA Illumina [185344] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084101 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.6: Pain in limb, hand, foot, fingers and toes 7,907 European ancestry cases, 378,626 European ancestry controls NA Affymetrix, Illumina [509490] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90080549 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34.8: Other specified disorders of nose and nasal sinuses (Gene-based burden) 3,165 European ancestry cases, 383,525 European ancestry controls NA Illumina [185326] 0 nasal disorder http://purl.obolibrary.org/obo/MONDO_0002436 GCST90084102 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G93: Other disorders of brain 2,591 European ancestry cases, 383,973 European ancestry controls NA Affymetrix, Illumina [509480] 0 brain disease http://www.ebi.ac.uk/efo/EFO_0005774 GCST90079858 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J35: Chronic diseases of tonsils and adenoids (Gene-based burden) 1,191 European ancestry cases, 385,993 European ancestry controls NA Illumina [185332] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084104 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G50: Disorders of trigeminal nerve 1,034 European ancestry cases, 385,495 European ancestry controls NA Affymetrix, Illumina [509476] 0 trigeminal nerve disease http://www.ebi.ac.uk/efo/EFO_0009569 GCST90079837 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J36: Peritonsillar abscess (Gene-based burden) 507 European ancestry cases, 387,145 European ancestry controls NA Illumina [185336] 0 peritonsillar abscess http://www.ebi.ac.uk/efo/EFO_0007429 GCST90084105 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.32: Type 2 diabetes mellitus with mild nonproliferative diabetic retinopathy 926 European ancestry cases, 385,625 European ancestry controls NA Affymetrix, Illumina [509472] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079738 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J38: Diseases of vocal cords and larynx, not elsewhere classified (Gene-based burden) 2,136 European ancestry cases, 385,278 European ancestry controls NA Illumina [185332] 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90084108 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.329.: Type 2 diabetes mellitus with mild nonproliferative diabetic retinopathy without macular edema 926 European ancestry cases, 385,625 European ancestry controls NA Affymetrix, Illumina [509472] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079737 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J38.3: Other diseases of vocal cords (Gene-based burden) 730 European ancestry cases, 387,195 European ancestry controls NA Illumina [185344] 0 Vocal cord dysfunction http://purl.obolibrary.org/obo/HP_0031801 GCST90084106 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.329.9: Type 2 diabetes mellitus with mild nonproliferative diabetic retinopathy without macular edema, unspecified eye 926 European ancestry cases, 385,625 European ancestry controls NA Affymetrix, Illumina [509472] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079736 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J38.7: Other diseases of larynx (Gene-based burden) 594 European ancestry cases, 387,336 European ancestry controls NA Illumina [185344] 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90084107 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.8: Other abnormalities of heart beat 672 European ancestry cases, 385,774 European ancestry controls NA Affymetrix, Illumina [509467] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90080753 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J39: Other diseases of upper respiratory tract (Gene-based burden) 1,109 European ancestry cases, 384,982 European ancestry controls NA Illumina [185319] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084110 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R69: Illness, unspecified 17,480 European ancestry cases, 369,056 European ancestry controls NA Affymetrix, Illumina [509461] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90080900 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J39.2: Other diseases of pharynx (Gene-based burden) 682 European ancestry cases, 386,581 European ancestry controls NA Illumina [185335] 0 disorder of pharynx http://purl.obolibrary.org/obo/MONDO_0020592 GCST90084109 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M66: Spontaneous rupture of synovium and tendon 802 European ancestry cases, 385,763 European ancestry controls NA Affymetrix, Illumina [509457] 0 Tendon rupture http://purl.obolibrary.org/obo/HP_0100550 GCST90080521 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J40: Bronchitis, not specified as acute or chronic (Gene-based burden) 1,447 European ancestry cases, 383,299 European ancestry controls NA Illumina [185284] 0 bronchitis http://www.ebi.ac.uk/efo/EFO_0009661 GCST90084111 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H72: Perforation of tympanic membrane 1,469 European ancestry cases, 385,072 European ancestry controls NA Affymetrix, Illumina [509447] 0 tympanic membrane perforation http://www.ebi.ac.uk/efo/EFO_0009472 GCST90079939 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J42: Unspecified chronic bronchitis (Gene-based burden) 575 European ancestry cases, 385,813 European ancestry controls NA Illumina [185313] 0 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST90084112 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I78: Diseases of capillaries 934 European ancestry cases, 385,558 European ancestry controls 1,261 European ancestry cases, 104,448 European ancestry controls Affymetrix, Illumina [509438] 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90080057 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34.8: Other specified disorders of nose and nasal sinuses 3,165 European ancestry cases, 383,525 European ancestry controls NA Affymetrix, Illumina [509599] 0 nasal disorder http://purl.obolibrary.org/obo/MONDO_0002436 GCST90080116 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J04: Acute laryngitis and tracheitis (Gene-based burden) 2,322 European ancestry cases, 377,480 European ancestry controls NA Illumina [185225] 0 acute laryngitis http://purl.obolibrary.org/obo/MONDO_0004777 GCST90084076 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13: Other specified diabetes mellitus 8,836 European ancestry cases, 377,872 European ancestry controls NA Affymetrix, Illumina [509594] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90079746 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J06: Acute upper respiratory infections of multiple and unspecified sites (Gene-based burden) 17,526 European ancestry cases, 335,507 European ancestry controls NA Illumina [184746] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084078 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.6: Fracture of lateral malleolus 1,103 European ancestry cases, 385,515 European ancestry controls NA Affymetrix, Illumina [509580] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081024 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J06.9: Acute upper respiratory infection, unspecified (Gene-based burden) 3,503 European ancestry cases, 374,275 European ancestry controls NA Illumina [185177] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084077 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21.9: Acute myocardial infarction, unspecified 5,398 European ancestry cases, 381,223 European ancestry controls NA Affymetrix, Illumina [509568] 0 acute myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008583 GCST90079972 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J11: Influenza due to unidentified influenza virus (Gene-based burden) 1,922 European ancestry cases, 377,148 European ancestry controls NA Illumina [185169] 0 influenza http://www.ebi.ac.uk/efo/EFO_0007328 GCST90084079 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N02: Recurrent and persistent hematuria 1,003 European ancestry cases, 385,638 European ancestry controls NA Affymetrix, Illumina [509562] 0 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST90080571 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J15: Bacterial pneumonia, not elsewhere classified (Gene-based burden) 715 European ancestry cases, 386,722 European ancestry controls NA Illumina [185341] 0 bacterial pneumonia http://www.ebi.ac.uk/efo/EFO_1001272 GCST90084080 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82.4: Acute embolism and thrombosis of deep veins of lower extremity 574 European ancestry cases, 386,116 European ancestry controls NA Affymetrix, Illumina [509556] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90080062 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18: Pneumonia, unspecified organism (Gene-based burden) 13,681 European ancestry cases, 371,904 European ancestry controls NA Illumina [185324] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90084084 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82.40: Acute embolism and thrombosis of unspecified deep veins of lower extremity 574 European ancestry cases, 386,116 European ancestry controls NA Affymetrix, Illumina [509556] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90080061 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18.0: Bronchopneumonia, unspecified organism (Gene-based burden) 1,056 European ancestry cases, 386,874 European ancestry controls NA Illumina [185344] 0 bronchopneumonia http://www.ebi.ac.uk/efo/EFO_0007184 GCST90084081 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82.409.: Acute embolism and thrombosis of unspecified deep veins of unspecified lower extremity 574 European ancestry cases, 386,116 European ancestry controls NA Affymetrix, Illumina [509556] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90080060 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18.1: Lobar pneumonia, unspecified organism (Gene-based burden) 8,262 European ancestry cases, 379,453 European ancestry controls NA Illumina [185343] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90084082 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.2: Fracture of nasal bones 800 European ancestry cases, 385,730 European ancestry controls NA Affymetrix, Illumina [509555] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080946 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18.9: Pneumonia, unspecified organism (Gene-based burden) 6,141 European ancestry cases, 380,836 European ancestry controls NA Illumina [185326] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90084083 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T39: Poisoning by, adverse effect of and underdosing of nonopioid analgesics, antipyretics and antirheumatics 2,026 European ancestry cases, 384,627 European ancestry controls NA Affymetrix, Illumina [509555] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081050 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J20: Acute bronchitis (Gene-based burden) 4,076 European ancestry cases, 373,308 European ancestry controls NA Illumina [185202] 0 Acute bronchitis http://purl.obolibrary.org/obo/HP_0012388 GCST90084086 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.3: Fracture of one rib 756 European ancestry cases, 385,854 European ancestry controls NA Affymetrix, Illumina [509547] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90080961 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J20.9: Acute bronchitis, unspecified (Gene-based burden) 3,052 European ancestry cases, 377,596 European ancestry controls NA Illumina [185247] 0 Acute bronchitis http://purl.obolibrary.org/obo/HP_0012388 GCST90084085 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50: Cervical disc disorders 2,103 European ancestry cases, 384,499 European ancestry controls 8,681 European ancestry cases, 87,769 European ancestry controls Affymetrix, Illumina [509538] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90080494 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J22: Unspecified acute lower respiratory infection (Gene-based burden) 31,920 European ancestry cases, 328,167 European ancestry controls NA Illumina [184905] 0 lower respiratory tract disease http://www.ebi.ac.uk/efo/EFO_0009433 GCST90084087 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M95: Other acquired deformities of musculoskeletal system and connective tissue 635 European ancestry cases, 386,003 European ancestry controls NA Affymetrix, Illumina [509533] 0 musculoskeletal system disease, connective tissue disease http://www.ebi.ac.uk/efo/EFO_0009676, http://www.ebi.ac.uk/efo/EFO_1001986 GCST90080569 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J43: Emphysema (Gene-based burden) 2,522 European ancestry cases, 385,122 European ancestry controls NA Illumina [185341] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90084114 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R59.0: Localized enlarged lymph nodes 2,468 European ancestry cases, 384,030 European ancestry controls NA Affymetrix, Illumina [509432] 0 Lymphadenopathy http://purl.obolibrary.org/obo/HP_0002716 GCST90080885 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J43.9: Emphysema, unspecified (Gene-based burden) 2,379 European ancestry cases, 385,541 European ancestry controls NA Illumina [185343] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90084113 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.1: Pleurisy 798 European ancestry cases, 385,742 European ancestry controls NA Affymetrix, Illumina [509430] 0 pleurisy http://www.ebi.ac.uk/efo/EFO_1001825 GCST90080780 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44: Other chronic obstructive pulmonary disease (Gene-based burden) 12,856 European ancestry cases, 373,496 European ancestry controls NA Illumina [185299] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90084119 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.6: Repeated falls 3,229 European ancestry cases, 383,252 European ancestry controls NA Affymetrix, Illumina [509418] 0 Abnormality of movement http://purl.obolibrary.org/obo/HP_0100022 GCST90080832 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.0: Chronic obstructive pulmonary disease with acute lower respiratory infection (Gene-based burden) 3,295 European ancestry cases, 384,635 European ancestry controls NA Illumina [185344] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90084115 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82: Other venous embolism and thrombosis 1,106 European ancestry cases, 385,404 European ancestry controls NA Affymetrix, Illumina [509407] 0 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90080063 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.1: Chronic obstructive pulmonary disease with (acute) exacerbation (Gene-based burden) 1,520 European ancestry cases, 386,410 European ancestry controls NA Illumina [185344] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90084116 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K14: Diseases of tongue 1,808 European ancestry cases, 384,676 European ancestry controls NA Affymetrix, Illumina [509403] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90080184 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.8: Other specified chronic obstructive pulmonary disease (Gene-based burden) 878 European ancestry cases, 387,052 European ancestry controls NA Illumina [185344] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90084117 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R26: Abnormalities of gait and mobility 3,394 European ancestry cases, 382,985 European ancestry controls NA Affymetrix, Illumina [509400] 0 Gait disturbance http://purl.obolibrary.org/obo/HP_0001288 GCST90080830 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.9: Chronic obstructive pulmonary disease, unspecified (Gene-based burden) 11,079 European ancestry cases, 375,462 European ancestry controls NA Illumina [185290] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90084118 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.8: Other specified bacterial agents as the cause of diseases classified elsewhere 6,173 European ancestry cases, 380,226 European ancestry controls NA Affymetrix, Illumina [509392] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079568 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45: Asthma (Gene-based burden) 39,436 European ancestry cases, 344,538 European ancestry controls NA Illumina [185285] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90084127 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20: Calculus of kidney and ureter 5,992 European ancestry cases, 380,427 European ancestry controls NA Affymetrix, Illumina [509389] 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90080588 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.0: Predominantly allergic asthma (Gene-based burden) 815 European ancestry cases, 387,115 European ancestry controls NA Illumina [185344] 0 atopic asthma http://www.ebi.ac.uk/efo/EFO_0010638 GCST90084120 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44.9: Chronic obstructive pulmonary disease, unspecified 11,079 European ancestry cases, 375,462 European ancestry controls NA Affymetrix, Illumina [509387] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90080132 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.9: Other and unspecified asthma (Gene-based burden) 38,114 European ancestry cases, 347,640 European ancestry controls NA Illumina [185317] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90084126 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81: Cholecystitis 3,403 European ancestry cases, 383,083 European ancestry controls NA Affymetrix, Illumina [509375] 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90080301 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.90: Unspecified asthma (Gene-based burden) 16,105 European ancestry cases, 368,789 European ancestry controls NA Illumina [185295] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90084123 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R25.1: Tremor, unspecified 1,055 European ancestry cases, 385,301 European ancestry controls NA Affymetrix, Illumina [509373] 0 Tremor http://purl.obolibrary.org/obo/HP_0001337 GCST90080826 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.901.: Unspecified asthma with (acute) exacerbation (Gene-based burden) 1,337 European ancestry cases, 384,644 European ancestry controls NA Illumina [185318] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90084121 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92.4: Street, highway and other paved roadways as the place of occurrence of the external cause 908 European ancestry cases, 385,483 European ancestry controls NA Affymetrix, Illumina [509365] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081173 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.909.: Unspecified asthma, uncomplicated (Gene-based burden) 16,035 European ancestry cases, 369,001 European ancestry controls NA Illumina [185287] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90084122 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J20.9: Acute bronchitis, unspecified 3,052 European ancestry cases, 377,596 European ancestry controls NA Affymetrix, Illumina [504325] 0 Acute bronchitis http://purl.obolibrary.org/obo/HP_0012388 GCST90080099 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.8: Other shoulder lesions (Gene-based burden) 1,778 European ancestry cases, 385,821 European ancestry controls NA Illumina [185343] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084522 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20.2: Paresthesia of skin 3,860 European ancestry cases, 376,820 European ancestry controls NA Affymetrix, Illumina [504325] 0 Paresthesia http://purl.obolibrary.org/obo/HP_0003401 GCST90080815 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M76: Enthesopathies, lower limb, excluding foot (Gene-based burden) 1,873 European ancestry cases, 380,906 European ancestry controls NA Illumina [185279] 0 enthesopathy http://www.ebi.ac.uk/efo/EFO_0009666 GCST90084524 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K30: Functional dyspepsia 17,044 European ancestry cases, 363,628 European ancestry controls NA Affymetrix, Illumina [504303] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90080209 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M77: Other enthesopathies (Gene-based burden) 9,756 European ancestry cases, 358,940 European ancestry controls NA Illumina [185022] 0 enthesopathy http://www.ebi.ac.uk/efo/EFO_0009666 GCST90084527 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32.9: Chronic sinusitis, unspecified 4,805 European ancestry cases, 375,925 European ancestry controls NA Affymetrix, Illumina [504292] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90080108 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M77.1: Lateral epicondylitis (Gene-based burden) 768 European ancestry cases, 387,162 European ancestry controls NA Illumina [185344] 0 lateral epicondylitis http://www.ebi.ac.uk/efo/EFO_1001896 GCST90084525 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.83: Encounter for screening for respiratory disorder NEC 3,410 European ancestry cases, 377,130 European ancestry controls NA Affymetrix, Illumina [504267] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081216 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M77.4: Metatarsalgia (Gene-based burden) 552 European ancestry cases, 386,812 European ancestry controls NA Illumina [185333] 0 metatarsalgia http://www.ebi.ac.uk/efo/EFO_1001370 GCST90084526 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93: Dislocation and sprain of joints and ligaments at ankle, foot and toe level 1,344 European ancestry cases, 379,230 European ancestry controls NA Affymetrix, Illumina [504223] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081043 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79: Other and unspecified soft tissue disorders, not elsewhere classified (Gene-based burden) 40,514 European ancestry cases, 312,278 European ancestry controls NA Illumina [184782] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084540 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.0: Personal history of diseases of the respiratory system 4,223 European ancestry cases, 376,238 European ancestry controls NA Affymetrix, Illumina [504140] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90081367 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.0: Rheumatism, unspecified (Gene-based burden) 1,093 European ancestry cases, 386,775 European ancestry controls NA Illumina [185344] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90084529 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R30: Pain associated with micturition 3,783 European ancestry cases, 376,929 European ancestry controls NA Affymetrix, Illumina [504134] 0 dysuria http://www.ebi.ac.uk/efo/EFO_0003901 GCST90080838 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.09: Rheumatism, unspecified (Gene-based burden) 657 European ancestry cases, 387,273 European ancestry controls NA Illumina [185344] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90084528 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R30.0: Dysuria 3,624 European ancestry cases, 377,076 European ancestry controls NA Affymetrix, Illumina [504122] 0 dysuria http://www.ebi.ac.uk/efo/EFO_0003901 GCST90080837 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.1: Myalgia (Gene-based burden) 1,350 European ancestry cases, 382,684 European ancestry controls NA Illumina [185292] 0 Myalgia http://purl.obolibrary.org/obo/HP_0003326 GCST90084530 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H83: Other diseases of inner ear 2,745 European ancestry cases, 377,741 European ancestry controls NA Affymetrix, Illumina [504067] 0 inner ear disease http://www.ebi.ac.uk/efo/EFO_0009672 GCST90079945 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.2: Neuralgia and neuritis, unspecified (Gene-based burden) 585 European ancestry cases, 386,972 European ancestry controls NA Illumina [185340] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90084531 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cerebrovascular disease - ischemic composite 9,143 European ancestry cases, 371,403 European ancestry controls NA Affymetrix, Illumina [504040] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90081470 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.6: Pain in limb, hand, foot, fingers and toes (Gene-based burden) 7,907 European ancestry cases, 378,626 European ancestry controls NA Illumina [185315] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90084535 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L02: Cutaneous abscess, furuncle and carbuncle 4,703 European ancestry cases, 375,791 European ancestry controls NA Affymetrix, Illumina [504015] 0 Cutaneous abscess http://purl.obolibrary.org/obo/HP_0031292 GCST90080326 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.65: Pain in thigh (Gene-based burden) 909 European ancestry cases, 387,021 European ancestry controls NA Illumina [185344] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90084532 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65: Synovitis and tenosynovitis 8,632 European ancestry cases, 371,813 European ancestry controls NA Affymetrix, Illumina [504008] 0 tenosynovitis http://www.ebi.ac.uk/efo/EFO_1001435 GCST90080520 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30: Vasomotor and allergic rhinitis (Gene-based burden) 7,482 European ancestry cases, 364,690 European ancestry controls NA Illumina [185084] 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90084090 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41.8: Other symptoms and signs involving cognitive functions and awareness 929 European ancestry cases, 385,683 European ancestry controls NA Affymetrix, Illumina [509529] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90080856 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30.1: Allergic rhinitis due to pollen (Gene-based burden) 1,201 European ancestry cases, 386,622 European ancestry controls NA Illumina [185344] 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90084088 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20: Angina pectoris 22,332 European ancestry cases, 364,233 European ancestry controls 6,645 European ancestry cases, 104,775 European ancestry controls Affymetrix, Illumina [509526] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90079968 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30.9: Allergic rhinitis, unspecified (Gene-based burden) 715 European ancestry cases, 383,607 European ancestry controls NA Illumina [185280] 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90084089 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S01: Open wound of head 4,083 European ancestry cases, 382,522 European ancestry controls NA Affymetrix, Illumina [509522] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90080944 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J31: Chronic rhinitis, nasopharyngitis and pharyngitis (Gene-based burden) 3,154 European ancestry cases, 376,940 European ancestry controls NA Illumina [185192] 0 rhinitis http://www.ebi.ac.uk/efo/EFO_0008521 GCST90084092 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H50: Other strabismus 1,194 European ancestry cases, 385,387 European ancestry controls NA Affymetrix, Illumina [509519] 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90079915 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J31.0: Chronic rhinitis (Gene-based burden) 1,949 European ancestry cases, 382,383 European ancestry controls NA Illumina [185292] 0 rhinitis http://www.ebi.ac.uk/efo/EFO_0008521 GCST90084091 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.0: Rheumatoid arthritis without rheumatoid factor 706 European ancestry cases, 385,886 European ancestry controls NA Affymetrix, Illumina [509518] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90080388 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32: Chronic sinusitis (Gene-based burden) 6,974 European ancestry cases, 369,561 European ancestry controls NA Illumina [185196] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90084095 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.1: Tinnitus 963 European ancestry cases, 385,606 European ancestry controls NA Affymetrix, Illumina [509516] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079953 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32.0: Chronic maxillary sinusitis (Gene-based burden) 666 European ancestry cases, 386,725 European ancestry controls NA Illumina [185333] 0 maxillary sinusitis http://www.ebi.ac.uk/efo/EFO_0007361 GCST90084093 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.9: Unspecified visual disturbance 667 European ancestry cases, 385,885 European ancestry controls NA Affymetrix, Illumina [509509] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90079922 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32.9: Chronic sinusitis, unspecified (Gene-based burden) 4,805 European ancestry cases, 375,925 European ancestry controls NA Illumina [185260] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90084094 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H18: Other disorders of cornea 1,087 European ancestry cases, 385,500 European ancestry controls NA Affymetrix, Illumina [509508] 0 corneal disease http://www.ebi.ac.uk/efo/EFO_0009464 GCST90079883 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33: Nasal polyp (Gene-based burden) 4,168 European ancestry cases, 382,509 European ancestry controls NA Illumina [185330] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90084099 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z11: Encounter for screening for infectious and parasitic diseases 923 European ancestry cases, 385,624 European ancestry controls NA Affymetrix, Illumina [509508] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081206 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33.0: Polyp of nasal cavity (Gene-based burden) 1,256 European ancestry cases, 386,674 European ancestry controls NA Illumina [185344] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90084096 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.84: Long term (current) use of oral hypoglycemic drugs 3,574 European ancestry cases, 383,035 European ancestry controls NA Affymetrix, Illumina [509506] 0 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90081324 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33.8: Other polyp of sinus (Gene-based burden) 740 European ancestry cases, 387,190 European ancestry controls NA Illumina [185344] 0 polyp http://www.ebi.ac.uk/efo/EFO_0000662 GCST90084097 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H20: Iridocyclitis 1,094 European ancestry cases, 385,475 European ancestry controls NA Affymetrix, Illumina [509505] 0 Iridocyclitis http://purl.obolibrary.org/obo/HP_0001094 GCST90079884 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33.9: Nasal polyp, unspecified (Gene-based burden) 2,073 European ancestry cases, 385,857 European ancestry controls NA Illumina [185344] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90084098 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.01: Encounter for initial prescription of contraceptives 1,304 European ancestry cases, 385,278 European ancestry controls NA Affymetrix, Illumina [509498] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081231 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34: Other and unspecified disorders of nose and nasal sinuses (Gene-based burden) 8,558 European ancestry cases, 373,094 European ancestry controls NA Illumina [185251] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084103 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59.0: Constipation 16,745 European ancestry cases, 363,304 European ancestry controls NA Affymetrix, Illumina [503683] 0 constipation disorder http://purl.obolibrary.org/obo/MONDO_0002203 GCST90080254 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M85: Other disorders of bone density and structure (Gene-based burden) 4,030 European ancestry cases, 377,290 European ancestry controls NA Illumina [185256] 0 Abnormality of bone mineral density http://purl.obolibrary.org/obo/HP_0004348 GCST90084549 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.00: Dyspnea, unspecified 4,013 European ancestry cases, 375,874 European ancestry controls NA Affymetrix, Illumina [503674] 0 Dyspnea http://purl.obolibrary.org/obo/HP_0002094 GCST90080765 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M85.8: Other specified disorders of bone density and structure (Gene-based burden) 1,471 European ancestry cases, 385,681 European ancestry controls NA Illumina [185335] 0 Abnormality of bone mineral density http://purl.obolibrary.org/obo/HP_0004348 GCST90084548 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.2: Immunization not carried out because of patient decision for other and unspecified reason 3,919 European ancestry cases, 376,013 European ancestry controls NA Affymetrix, Illumina [503637] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081226 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M86: Osteomyelitis (Gene-based burden) 763 European ancestry cases, 386,454 European ancestry controls NA Illumina [185333] 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90084550 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z76: Persons encountering health services in other circumstances 5,561 European ancestry cases, 374,354 European ancestry controls NA Affymetrix, Illumina [503635] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081323 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M87: Osteonecrosis (Gene-based burden) 669 European ancestry cases, 387,134 European ancestry controls NA Illumina [185332] 0 osteonecrosis http://www.ebi.ac.uk/efo/EFO_0004259 GCST90084551 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R03: Abnormal blood-pressure reading, without diagnosis 7,318 European ancestry cases, 372,605 European ancestry controls NA Affymetrix, Illumina [503628] 0 Abnormal systemic blood pressure http://purl.obolibrary.org/obo/HP_0030972 GCST90080760 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M89: Other disorders of bone (Gene-based burden) 1,953 European ancestry cases, 385,201 European ancestry controls NA Illumina [185334] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90084553 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.8: Other specified complications of internal orthopedic prosthetic devices, implants and grafts 6,289 European ancestry cases, 373,482 European ancestry controls NA Affymetrix, Illumina [503598] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081082 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M89.9: Disorder of bone, unspecified (Gene-based burden) 942 European ancestry cases, 386,978 European ancestry controls NA Illumina [185344] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90084552 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.89: Other specified symptoms and signs involving the circulatory and respiratory systems 2,494 European ancestry cases, 377,527 European ancestry controls NA Affymetrix, Illumina [503594] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90080782 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M94: Other disorders of cartilage (Gene-based burden) 1,122 European ancestry cases, 384,496 European ancestry controls NA Illumina [185291] 0 cartilage disease http://www.ebi.ac.uk/efo/EFO_0005802 GCST90084554 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52: Fracture of forearm 8,168 European ancestry cases, 371,727 European ancestry controls NA Affymetrix, Illumina [503585] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080991 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M95: Other acquired deformities of musculoskeletal system and connective tissue (Gene-based burden) 635 European ancestry cases, 386,003 European ancestry controls NA Illumina [185329] 0 musculoskeletal system disease, connective tissue disease http://www.ebi.ac.uk/efo/EFO_0009676, http://www.ebi.ac.uk/efo/EFO_1001986 GCST90084555 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30: Cystitis 7,658 European ancestry cases, 372,291 European ancestry controls NA Affymetrix, Illumina [503581] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90080599 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M96: Intraoperative and postprocedural complications and disorders of musculoskeletal system, not elsewhere classified (Gene-based burden) 588 European ancestry cases, 387,322 European ancestry controls NA Illumina [185344] 0 musculoskeletal system disease http://www.ebi.ac.uk/efo/EFO_0009676 GCST90084556 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.0: Abnormal glucose 3,431 European ancestry cases, 376,474 European ancestry controls NA Affymetrix, Illumina [503551] 0 Abnormal glucose homeostasis http://purl.obolibrary.org/obo/HP_0011014 GCST90080904 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N02: Recurrent and persistent hematuria (Gene-based burden) 1,003 European ancestry cases, 385,638 European ancestry controls NA Illumina [185328] 0 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST90084557 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J04: Acute laryngitis and tracheitis 2,322 European ancestry cases, 377,480 European ancestry controls NA Affymetrix, Illumina [503527] 0 acute laryngitis http://purl.obolibrary.org/obo/MONDO_0004777 GCST90080090 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N03: Chronic nephritic syndrome (Gene-based burden) 978 European ancestry cases, 386,890 European ancestry controls NA Illumina [185344] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90084559 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.84: Pain due to internal orthopedic prosthetic devices, implants and grafts 4,278 European ancestry cases, 375,391 European ancestry controls NA Affymetrix, Illumina [503504] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081081 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N03.9: Chronic nephritic syndrome with unspecified morphologic changes (Gene-based burden) 918 European ancestry cases, 387,010 European ancestry controls NA Illumina [185344] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90084558 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V89.2: Person injured in unspecified motor-vehicle accident, traffic 1,485 European ancestry cases, 378,407 European ancestry controls NA Affymetrix, Illumina [503489] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081097 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13.5: Crossing vessel and stricture of ureter without hydronephrosis (Gene-based burden) 597 European ancestry cases, 387,333 European ancestry controls NA Illumina [185344] 0 stricture or kinking of ureter http://purl.obolibrary.org/obo/MONDO_0002674 GCST90084563 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.6: Encounter for screening for cardiovascular disorders 5,026 European ancestry cases, 374,645 European ancestry controls NA Affymetrix, Illumina [503352] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081215 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N17: Acute kidney failure (Gene-based burden) 7,925 European ancestry cases, 379,873 European ancestry controls NA Illumina [185344] 0 acute kidney failure http://purl.obolibrary.org/obo/MONDO_0002492 GCST90084566 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J00: Acute nasopharyngitis [common cold] 2,558 European ancestry cases, 377,078 European ancestry controls NA Affymetrix, Illumina [503347] 0 common cold http://www.ebi.ac.uk/efo/EFO_0007214 GCST90080084 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N17.9: Acute kidney failure, unspecified (Gene-based burden) 7,852 European ancestry cases, 380,074 European ancestry controls NA Illumina [185344] 0 acute kidney failure http://purl.obolibrary.org/obo/MONDO_0002492 GCST90084565 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78: Adverse effects, not elsewhere classified 2,437 European ancestry cases, 377,187 European ancestry controls NA Affymetrix, Illumina [503347] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081066 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18: Chronic kidney disease (Gene-based burden) 10,144 European ancestry cases, 372,699 European ancestry controls NA Illumina [185242] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90084570 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-alcoholic fatty liver disease - Composite 3,220 European ancestry cases, 376,493 European ancestry controls NA Affymetrix, Illumina [503334] 0 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90081501 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18.3: Chronic kidney disease, stage 3 (moderate) (Gene-based burden) 3,948 European ancestry cases, 383,982 European ancestry controls NA Illumina [185344] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90084567 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22: Melanocytic nevi 7,622 European ancestry cases, 371,925 European ancestry controls NA Affymetrix, Illumina [503285] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90079677 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18.4: Chronic kidney disease, stage 4 (severe) (Gene-based burden) 545 European ancestry cases, 387,385 European ancestry controls NA Illumina [185344] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90084568 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J03: Acute tonsillitis 2,733 European ancestry cases, 376,762 European ancestry controls NA Affymetrix, Illumina [503214] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90080089 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18.9: Chronic kidney disease, unspecified (Gene-based burden) 3,916 European ancestry cases, 384,014 European ancestry controls NA Illumina [185344] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90084569 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.8: Procedure and treatment not carried out for other reasons 20,562 European ancestry cases, 358,695 European ancestry controls NA Affymetrix, Illumina [503143] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081290 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N19: Unspecified kidney failure (Gene-based burden) 1,792 European ancestry cases, 385,939 European ancestry controls NA Illumina [185343] 0 kidney failure http://www.ebi.ac.uk/efo/EFO_1002048 GCST90084571 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92: Personal history of medical treatment 42,783 European ancestry cases, 336,594 European ancestry controls 1,839 European ancestry cases, 34,686 European ancestry controls Affymetrix, Illumina [503139] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081411 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20: Calculus of kidney and ureter (Gene-based burden) 5,992 European ancestry cases, 380,427 European ancestry controls NA Illumina [185322] 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90084574 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93: Abnormal findings on diagnostic imaging of other body structures 5,929 European ancestry cases, 373,345 European ancestry controls NA Affymetrix, Illumina [503129] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90080933 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20.0: Calculus of kidney (Gene-based burden) 3,998 European ancestry cases, 383,150 European ancestry controls NA Illumina [185327] 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90084572 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.3: Sciatica 5,711 European ancestry cases, 373,607 European ancestry controls NA Affymetrix, Illumina [503093] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90080505 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N20.1: Calculus of ureter (Gene-based burden) 2,766 European ancestry cases, 385,149 European ancestry controls NA Illumina [185344] 0 ureterolithiasis http://www.ebi.ac.uk/efo/EFO_1001228 GCST90084573 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N52.9: Male erectile dysfunction, unspecified 6,768 European ancestry cases, 372,700 European ancestry controls NA Affymetrix, Illumina [503053] 0 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST90080636 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N21: Calculus of lower urinary tract (Gene-based burden) 979 European ancestry cases, 386,821 European ancestry controls NA Illumina [185343] 0 ureterolithiasis http://www.ebi.ac.uk/efo/EFO_1001228 GCST90084576 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F43: Reaction to severe stress, and adjustment disorders 4,612 European ancestry cases, 374,861 European ancestry controls NA Affymetrix, Illumina [503048] 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90079813 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N21.0: Calculus in bladder (Gene-based burden) 886 European ancestry cases, 387,039 European ancestry controls NA Illumina [185344] 0 bladder calculus http://www.ebi.ac.uk/efo/EFO_1000839 GCST90084575 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.66: Pain in lower leg (Gene-based burden) 3,465 European ancestry cases, 384,465 European ancestry controls NA Illumina [185344] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90084533 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01: Other inflammation of eyelid 2,724 European ancestry cases, 377,649 European ancestry controls NA Affymetrix, Illumina [503985] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90079867 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.67: Pain in foot and toes (Gene-based burden) 724 European ancestry cases, 386,976 European ancestry controls NA Illumina [185340] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90084534 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R50: Fever of other and unknown origin 6,970 European ancestry cases, 373,504 European ancestry controls NA Affymetrix, Illumina [503951] 0 fever of unknown origin http://www.ebi.ac.uk/efo/EFO_0003952 GCST90080869 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.7: Fibromyalgia (Gene-based burden) 1,545 European ancestry cases, 386,385 European ancestry controls NA Illumina [185344] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90084537 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R50.9: Fever, unspecified 6,471 European ancestry cases, 373,978 European ancestry controls NA Affymetrix, Illumina [503927] 0 fever of unknown origin http://www.ebi.ac.uk/efo/EFO_0003952 GCST90080868 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.79: Fibromyalgia (Gene-based burden) 539 European ancestry cases, 387,391 European ancestry controls NA Illumina [185344] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90084536 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L85: Other epidermal thickening 2,073 European ancestry cases, 378,173 European ancestry controls NA Affymetrix, Illumina [503901] 0 Epidermal thickening http://purl.obolibrary.org/obo/HP_0011368 GCST90080372 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.8: Other specified soft tissue disorders (Gene-based burden) 6,170 European ancestry cases, 380,041 European ancestry controls NA Illumina [185319] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084539 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J31: Chronic rhinitis, nasopharyngitis and pharyngitis 3,154 European ancestry cases, 376,940 European ancestry controls NA Affymetrix, Illumina [503886] 0 rhinitis http://www.ebi.ac.uk/efo/EFO_0008521 GCST90080106 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.86: Other specified soft tissue disorders (Gene-based burden) 3,840 European ancestry cases, 384,090 European ancestry controls NA Illumina [185344] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084538 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z84: Family history of other conditions 1,226 European ancestry cases, 379,055 European ancestry controls NA Affymetrix, Illumina [503858] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081346 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M80: Osteoporosis with current pathological fracture (Gene-based burden) 1,190 European ancestry cases, 386,550 European ancestry controls NA Illumina [185343] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90084542 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R89: Abnormal findings in specimens from other organs, systems and tissues 3,179 European ancestry cases, 376,895 European ancestry controls NA Affymetrix, Illumina [503770] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080926 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M80.9: Unspecified osteoporosis with pathological fracture (Gene-based burden) 815 European ancestry cases, 387,115 European ancestry controls NA Illumina [185344] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90084541 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.9: Unspecified hearing loss 6,065 European ancestry cases, 374,041 European ancestry controls NA Affymetrix, Illumina [503757] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90079950 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81: Osteoporosis without current pathological fracture (Gene-based burden) 10,456 European ancestry cases, 373,627 European ancestry controls NA Illumina [185291] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90084545 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62: Fracture at wrist and hand level 3,764 European ancestry cases, 376,129 European ancestry controls NA Affymetrix, Illumina [503751] 0 wrist fracture http://www.ebi.ac.uk/efo/EFO_0009515 GCST90081002 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81.9: Osteoporosis, unspecified (Gene-based burden) 8,206 European ancestry cases, 379,724 European ancestry controls NA Illumina [185344] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90084544 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84: Complications of internal orthopedic prosthetic devices, implants and grafts 10,104 European ancestry cases, 369,829 European ancestry controls NA Affymetrix, Illumina [503750] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081083 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M81.99: Osteoporosis, unspecified (Gene-based burden) 3,895 European ancestry cases, 384,035 European ancestry controls NA Illumina [185344] 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90084543 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L91: Hypertrophic disorders of skin 3,255 European ancestry cases, 376,796 European ancestry controls NA Affymetrix, Illumina [503742] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080379 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M84: Disorder of continuity of bone (Gene-based burden) 2,120 European ancestry cases, 383,442 European ancestry controls NA Illumina [185305] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90084547 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R03.0: Elevated blood-pressure reading, without diagnosis of hypertension 5,889 European ancestry cases, 374,125 European ancestry controls NA Affymetrix, Illumina [503697] 0 Abnormal systemic blood pressure http://purl.obolibrary.org/obo/HP_0030972 GCST90080758 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M84.1: Nonunion of fracture [pseudarthrosis] (Gene-based burden) 1,026 European ancestry cases, 386,904 European ancestry controls NA Illumina [185344] 0 fractures, ununited http://www.ebi.ac.uk/efo/EFO_0009707 GCST90084546 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92.41: Street and highway as the place of occurrence of the external cause 908 European ancestry cases, 385,483 European ancestry controls NA Affymetrix, Illumina [509365] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081172 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.99: Other asthma (Gene-based burden) 1,983 European ancestry cases, 384,056 European ancestry controls NA Illumina [185318] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90084125 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92.410.: Unspecified street and highway as the place of occurrence of the external cause 908 European ancestry cases, 385,483 European ancestry controls NA Affymetrix, Illumina [509365] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081171 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.998.: Other asthma (Gene-based burden) 1,983 European ancestry cases, 384,056 European ancestry controls NA Illumina [185318] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90084124 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96: Other bacterial agents as the cause of diseases classified elsewhere 11,084 European ancestry cases, 375,265 European ancestry controls NA Affymetrix, Illumina [509357] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079569 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J47: Bronchiectasis (Gene-based burden) 3,053 European ancestry cases, 384,169 European ancestry controls NA Illumina [185334] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90084128 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.1: Hypo-osmolality and hyponatremia 3,625 European ancestry cases, 382,688 European ancestry controls NA Affymetrix, Illumina [509342] 0 Abnormality of metabolism/homeostasis http://purl.obolibrary.org/obo/HP_0001939 GCST90079774 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J69: Pneumonitis due to solids and liquids (Gene-based burden) 1,140 European ancestry cases, 386,749 European ancestry controls NA Illumina [185344] 0 pneumonitis http://www.ebi.ac.uk/efo/EFO_1001991 GCST90084130 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.43: Encounter for surveillance of intrauterine contraceptive device 656 European ancestry cases, 385,702 European ancestry controls NA Affymetrix, Illumina [509341] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081237 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J69.0: Pneumonitis due to inhalation of food and vomit (Gene-based burden) 1,101 European ancestry cases, 386,829 European ancestry controls NA Illumina [185344] 0 pneumonitis http://www.ebi.ac.uk/efo/EFO_1001991 GCST90084129 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L91.8: Other hypertrophic disorders of the skin 1,196 European ancestry cases, 385,192 European ancestry controls NA Affymetrix, Illumina [509331] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080378 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J81: Pulmonary edema (Gene-based burden) 688 European ancestry cases, 387,127 European ancestry controls NA Illumina [185339] 0 pulmonary edema http://www.ebi.ac.uk/efo/EFO_1001134 GCST90084131 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J42: Unspecified chronic bronchitis 575 European ancestry cases, 385,813 European ancestry controls NA Affymetrix, Illumina [509328] 0 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST90080126 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J84: Other interstitial pulmonary diseases (Gene-based burden) 1,577 European ancestry cases, 386,114 European ancestry controls NA Illumina [185344] 0 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90084133 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04: Other nontoxic goiter 2,457 European ancestry cases, 384,010 European ancestry controls NA Affymetrix, Illumina [509325] 0 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90079726 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J84.1: Other interstitial pulmonary diseases with fibrosis (Gene-based burden) 1,304 European ancestry cases, 386,553 European ancestry controls NA Illumina [185344] 0 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90084132 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R27: Other lack of coordination 775 European ancestry cases, 385,556 European ancestry controls NA Affymetrix, Illumina [509311] 0 Abnormality of movement http://purl.obolibrary.org/obo/HP_0100022 GCST90080831 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N12: Tubulo-interstitial nephritis, not specified as acute or chronic (Gene-based burden) 1,223 European ancestry cases, 386,282 European ancestry controls NA Illumina [185342] 0 nephritis http://www.ebi.ac.uk/efo/EFO_1002050 GCST90084560 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R60: Edema, not elsewhere classified 5,259 European ancestry cases, 374,500 European ancestry controls NA Affymetrix, Illumina [503471] 0 edema http://www.ebi.ac.uk/efo/EFO_0009373 GCST90080890 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13: Obstructive and reflux uropathy (Gene-based burden) 3,650 European ancestry cases, 383,346 European ancestry controls NA Illumina [185337] 0 urinary tract obstruction http://www.ebi.ac.uk/efo/EFO_0009571 GCST90084564 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V89: Motor- or nonmotor-vehicle accident, type of vehicle unspecified 1,541 European ancestry cases, 378,330 European ancestry controls NA Affymetrix, Illumina [503469] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081098 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13.2: Hydronephrosis with renal and ureteral calculous obstruction (Gene-based burden) 892 European ancestry cases, 387,038 European ancestry controls NA Illumina [185344] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90084561 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.90: Unspecified hearing loss, unspecified ear 2,026 European ancestry cases, 377,733 European ancestry controls NA Affymetrix, Illumina [503396] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90079949 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13.3: Other and unspecified hydronephrosis (Gene-based burden) 1,654 European ancestry cases, 386,276 European ancestry controls NA Illumina [185344] 0 hydronephrosis http://www.ebi.ac.uk/efo/EFO_0005562 GCST90084562 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.0: Urinary tract infection, site not specified 19,361 European ancestry cases, 360,258 European ancestry controls NA Affymetrix, Illumina [503379] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90080611 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K11: Diseases of salivary glands 1,546 European ancestry cases, 384,408 European ancestry controls NA Affymetrix, Illumina [508940] 0 salivary gland disease http://www.ebi.ac.uk/efo/EFO_0008581 GCST90080177 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.1: Other acute gastritis (Gene-based burden) 943 European ancestry cases, 386,987 European ancestry controls NA Illumina [185344] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90084188 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R80: Proteinuria 1,218 European ancestry cases, 384,665 European ancestry controls NA Affymetrix, Illumina [508937] 0 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90080913 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.5: Unspecified chronic gastritis (Gene-based burden) 3,998 European ancestry cases, 383,932 European ancestry controls NA Illumina [185344] 0 chronic gastritis http://www.ebi.ac.uk/efo/EFO_0000337 GCST90084189 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22: Other diseases of esophagus 12,840 European ancestry cases, 373,098 European ancestry controls NA Affymetrix, Illumina [508936] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90080195 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.6: Other gastritis (Gene-based burden) 6,987 European ancestry cases, 380,943 European ancestry controls NA Illumina [185344] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90084190 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G57: Mononeuropathies of lower limb 2,301 European ancestry cases, 383,611 European ancestry controls NA Affymetrix, Illumina [508931] 0 mononeuropathy http://www.ebi.ac.uk/efo/EFO_0009558 GCST90079848 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.7: Gastritis, unspecified (Gene-based burden) 19,439 European ancestry cases, 366,238 European ancestry controls NA Illumina [185311] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90084192 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.0: Procedure and treatment not carried out because of contraindication 11,131 European ancestry cases, 374,692 European ancestry controls NA Affymetrix, Illumina [508929] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081288 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.70: Gastritis, unspecified, without bleeding (Gene-based burden) 747 European ancestry cases, 383,610 European ancestry controls NA Illumina [185301] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90084191 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M71: Other bursopathies 1,374 European ancestry cases, 384,525 European ancestry controls NA Affymetrix, Illumina [508918] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90080528 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.8: Duodenitis (Gene-based burden) 9,283 European ancestry cases, 378,647 European ancestry controls NA Illumina [185344] 0 duodenitis http://purl.obolibrary.org/obo/MONDO_0004627 GCST90084193 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K26: Duodenal ulcer 4,256 European ancestry cases, 381,602 European ancestry controls NA Affymetrix, Illumina [508916] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90080199 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K30: Functional dyspepsia (Gene-based burden) 17,044 European ancestry cases, 363,628 European ancestry controls NA Illumina [185258] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90084195 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93.1: Abnormal findings on diagnostic imaging of heart and coronary circulation 917 European ancestry cases, 385,023 European ancestry controls NA Affymetrix, Illumina [508914] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90080930 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31: Other diseases of stomach and duodenum (Gene-based burden) 10,072 European ancestry cases, 377,247 European ancestry controls NA Illumina [185320] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084199 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S92.30: Fracture of unspecified metatarsal bone(s) 635 European ancestry cases, 385,120 European ancestry controls NA Affymetrix, Illumina [508908] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90081037 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31.7: Polyp of stomach and duodenum (Gene-based burden) 6,198 European ancestry cases, 381,584 European ancestry controls NA Illumina [185335] 0 stomach polyp http://purl.obolibrary.org/obo/MONDO_0008277 GCST90084196 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z73: Problems related to life management difficulty 1,198 European ancestry cases, 384,766 European ancestry controls NA Affymetrix, Illumina [508896] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081316 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31.8: Other specified diseases of stomach and duodenum (Gene-based burden) 3,075 European ancestry cases, 384,823 European ancestry controls NA Illumina [185341] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90084197 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.1: Personal history of infectious and parasitic diseases 2,974 European ancestry cases, 382,859 European ancestry controls NA Affymetrix, Illumina [508877] 0 parasitic infection http://www.ebi.ac.uk/efo/EFO_0001067 GCST90081356 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31.9: Disease of stomach and duodenum, unspecified (Gene-based burden) 883 European ancestry cases, 386,985 European ancestry controls NA Illumina [185342] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90084198 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J03.9: Acute tonsillitis, unspecified 942 European ancestry cases, 384,892 European ancestry controls NA Affymetrix, Illumina [508869] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90080088 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K35: Acute appendicitis (Gene-based burden) 3,368 European ancestry cases, 384,092 European ancestry controls NA Illumina [185342] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90084202 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.319.: Type 2 diabetes mellitus with unspecified diabetic retinopathy without macular edema 2,563 European ancestry cases, 383,369 European ancestry controls NA Affymetrix, Illumina [508868] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079734 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22: Other diseases of esophagus (Gene-based burden) 12,840 European ancestry cases, 373,098 European ancestry controls NA Illumina [185318] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90084181 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J06.9: Acute upper respiratory infection, unspecified 3,503 European ancestry cases, 374,275 European ancestry controls NA Affymetrix, Illumina [501590] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080091 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N45: Orchitis and epididymitis (Gene-based burden) 1,983 European ancestry cases, 171,102 European ancestry controls NA Illumina [175341] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90084612 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59: Other functional intestinal disorders 18,263 European ancestry cases, 359,286 European ancestry controls NA Affymetrix, Illumina [501513] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080255 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N45.9: Orchitis, epididymitis and epididymo-orchitis without abscess (Gene-based burden) 931 European ancestry cases, 193,674 European ancestry controls NA Illumina [177570] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90084611 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.9: Unspecified abdominal pain 4,176 European ancestry cases, 373,650 European ancestry controls NA Affymetrix, Illumina [501512] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90080791 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N47: Disorders of prepuce (Gene-based burden) 2,528 European ancestry cases, 173,085 European ancestry controls NA Illumina [175580] 0 phimosis http://www.ebi.ac.uk/efo/EFO_1001104 GCST90084613 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.90: Unspecified osteoarthritis, unspecified site 4,544 European ancestry cases, 372,887 European ancestry controls NA Affymetrix, Illumina [501428] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080421 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48: Other disorders of penis (Gene-based burden) 3,394 European ancestry cases, 169,501 European ancestry controls NA Illumina [175259] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90084617 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56.8: Other problems related to employment 5,671 European ancestry cases, 371,701 European ancestry controls NA Affymetrix, Illumina [501426] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081295 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48.1: Balanitis (Gene-based burden) 591 European ancestry cases, 174,673 European ancestry controls NA Illumina [175521] 0 balanitis http://www.ebi.ac.uk/efo/EFO_1000833 GCST90084614 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56.89: Other problems related to employment 5,671 European ancestry cases, 371,702 European ancestry controls NA Affymetrix, Illumina [501426] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081294 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48.6: Induration penis plastica (Gene-based burden) 937 European ancestry cases, 193,668 European ancestry controls NA Illumina [177570] 0 Penile Fibromatosis http://www.ebi.ac.uk/efo/EFO_1000466 GCST90084615 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J20: Acute bronchitis 4,076 European ancestry cases, 373,308 European ancestry controls NA Affymetrix, Illumina [501398] 0 Acute bronchitis http://purl.obolibrary.org/obo/HP_0012388 GCST90080100 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N48.8: Other specified disorders of penis (Gene-based burden) 524 European ancestry cases, 175,725 European ancestry controls NA Illumina [175627] 0 penile disorder http://purl.obolibrary.org/obo/MONDO_0002036 GCST90084616 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R35: Polyuria 7,550 European ancestry cases, 369,997 European ancestry controls NA Affymetrix, Illumina [501374] 0 Polyuria http://purl.obolibrary.org/obo/HP_0000103 GCST90080847 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50: Other and unspecified disorders of male genital organs (Gene-based burden) 5,205 European ancestry cases, 164,191 European ancestry controls NA Illumina [175022] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90084621 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.8: Other specified symptoms and signs involving the circulatory and respiratory systems 3,641 European ancestry cases, 373,833 European ancestry controls NA Affymetrix, Illumina [501363] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90080783 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50.1: Vascular disorders of male genital organs (Gene-based burden) 688 European ancestry cases, 175,465 European ancestry controls NA Illumina [175621] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90084618 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62: Other diseases of anus and rectum 30,248 European ancestry cases, 347,295 European ancestry controls NA Affymetrix, Illumina [501354] 0 anus disease, rectal disease http://www.ebi.ac.uk/efo/EFO_0009660, http://www.ebi.ac.uk/efo/EFO_0009685 GCST90080268 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50.8: Other specified disorders of male genital organs (Gene-based burden) 3,016 European ancestry cases, 171,235 European ancestry controls NA Illumina [175487] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90084620 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol liver disease - composite 1,120 European ancestry cases, 376,493 European ancestry controls NA Affymetrix, Illumina [501324] 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90081447 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N50.89: Other specified disorders of the male genital organs (Gene-based burden) 585 European ancestry cases, 385,274 European ancestry controls NA Illumina [185287] 0 male reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009555 GCST90084619 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.82: Chronic fatigue, unspecified 4,932 European ancestry cases, 372,337 European ancestry controls NA Affymetrix, Illumina [501313] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90080875 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N52: Male erectile dysfunction (Gene-based burden) 6,768 European ancestry cases, 372,688 European ancestry controls NA Illumina [185190] 0 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST90084623 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.1: Ulcer of esophagus (Gene-based burden) 5,969 European ancestry cases, 381,961 European ancestry controls NA Illumina [185344] 0 esophageal ulcer http://purl.obolibrary.org/obo/MONDO_0044782 GCST90084175 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.901.: Unspecified asthma with (acute) exacerbation 1,337 European ancestry cases, 384,644 European ancestry controls NA Affymetrix, Illumina [509015] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90080135 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.2: Esophageal obstruction (Gene-based burden) 2,458 European ancestry cases, 385,407 European ancestry controls NA Illumina [185344] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90084176 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.50: Unspecified fracture of the lower end of radius 4,489 European ancestry cases, 381,436 European ancestry controls NA Affymetrix, Illumina [509013] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080987 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.4: Dyskinesia of esophagus (Gene-based burden) 629 European ancestry cases, 387,219 European ancestry controls NA Illumina [185344] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90084177 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F40: Phobic anxiety disorders 1,328 European ancestry cases, 384,738 European ancestry controls NA Affymetrix, Illumina [509012] 0 phobic disorder http://www.ebi.ac.uk/efo/EFO_1001908 GCST90079807 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.7: Barrett's esophagus (Gene-based burden) 3,950 European ancestry cases, 383,962 European ancestry controls NA Illumina [185343] 0 Barrett's esophagus http://www.ebi.ac.uk/efo/EFO_0000280 GCST90084178 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y92: Place of occurrence of the external cause 942 European ancestry cases, 385,084 European ancestry controls NA Affymetrix, Illumina [509011] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081174 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.8: Other specified diseases of esophagus (Gene-based burden) 1,480 European ancestry cases, 386,448 European ancestry controls NA Illumina [185344] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90084179 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.3: Family history of malignant neoplasm of breast 2,022 European ancestry cases, 384,012 European ancestry controls 2,873 European ancestry cases, 33,532 European ancestry controls Affymetrix, Illumina [509007] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90081331 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.9: Disease of esophagus, unspecified (Gene-based burden) 690 European ancestry cases, 387,136 European ancestry controls NA Illumina [185342] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90084180 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H54: Blindness and low vision 1,725 European ancestry cases, 384,291 European ancestry controls NA Affymetrix, Illumina [508991] 0 Visual impairment http://purl.obolibrary.org/obo/HP_0000505 GCST90079924 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K25: Gastric ulcer (Gene-based burden) 5,549 European ancestry cases, 381,689 European ancestry controls NA Illumina [185343] 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90084183 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R80.9: Proteinuria, unspecified 847 European ancestry cases, 385,062 European ancestry controls NA Affymetrix, Illumina [508973] 0 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90080912 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K25.9: Gastric ulcer, unspecified as acute or chronic, without hemorrhage or perforation (Gene-based burden) 4,625 European ancestry cases, 383,304 European ancestry controls NA Illumina [185344] 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90084182 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.00: Fracture of unspecified part of clavicle 1,037 European ancestry cases, 384,849 European ancestry controls NA Affymetrix, Illumina [508957] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080974 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K26: Duodenal ulcer (Gene-based burden) 4,256 European ancestry cases, 381,602 European ancestry controls NA Illumina [185327] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90084185 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.99: Other asthma 1,983 European ancestry cases, 384,056 European ancestry controls NA Affymetrix, Illumina [508950] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90080139 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K26.9: Duodenal ulcer, unspecified as acute or chronic, without hemorrhage or perforation (Gene-based burden) 2,705 European ancestry cases, 385,225 European ancestry controls NA Illumina [185344] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90084184 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.998.: Other asthma 1,983 European ancestry cases, 384,056 European ancestry controls NA Affymetrix, Illumina [508950] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90080138 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K27: Peptic ulcer, site unspecified (Gene-based burden) 583 European ancestry cases, 386,834 European ancestry controls NA Illumina [185342] 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90084186 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51: Complications and ill-defined descriptions of heart disease 6,712 European ancestry cases, 379,168 European ancestry controls 4,044 European ancestry cases, 93,286 European ancestry controls Affymetrix, Illumina [508948] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90080027 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29: Gastritis and duodenitis (Gene-based burden) 37,321 European ancestry cases, 345,285 European ancestry controls NA Illumina [185265] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90084194 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.01: Impaired fasting glucose 587 European ancestry cases, 385,372 European ancestry controls NA Affymetrix, Illumina [508944] 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90080901 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.0: Acute gastritis (Gene-based burden) 526 European ancestry cases, 387,388 European ancestry controls NA Illumina [185344] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90084187 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N76: Other inflammation of vagina and vulva (Gene-based burden) 1,782 European ancestry cases, 206,704 European ancestry controls NA Illumina [179740] 0 vaginal inflammation http://www.ebi.ac.uk/efo/EFO_0005757 GCST90084633 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21: Gastro-esophageal reflux disease 34,552 European ancestry cases, 342,096 European ancestry controls NA Affymetrix, Illumina [500618] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90080188 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80: Endometriosis (Gene-based burden) 4,475 European ancestry cases, 205,856 European ancestry controls NA Illumina [179840] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90084638 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D18: Hemangioma and lymphangioma, any site 2,097 European ancestry cases, 384,010 European ancestry controls NA Affymetrix, Illumina [509020] 0 lymphangioma, hemangioma http://purl.obolibrary.org/obo/MONDO_0002013, http://www.ebi.ac.uk/efo/EFO_1000635 GCST90079671 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K35.0: Acute appendicitis with generalized peritonitis (Gene-based burden) 729 European ancestry cases, 387,201 European ancestry controls NA Illumina [185344] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90084200 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z74.1: Need for assistance with personal care 584 European ancestry cases, 385,416 European ancestry controls NA Affymetrix, Illumina [508862] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081318 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K35.9: Acute appendicitis, unspecified (Gene-based burden) 1,587 European ancestry cases, 386,343 European ancestry controls NA Illumina [185344] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90084201 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63.8: Other symptoms and signs concerning food and fluid intake 896 European ancestry cases, 385,040 European ancestry controls NA Affymetrix, Illumina [508860] 0 sign or symptom concerning food and fluid intake http://www.ebi.ac.uk/efo/EFO_0009825 GCST90080895 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K37: Unspecified appendicitis (Gene-based burden) 543 European ancestry cases, 387,117 European ancestry controls NA Illumina [185342] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90084203 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.60: Fracture of unspecified phalanx of finger 1,048 European ancestry cases, 384,698 European ancestry controls NA Affymetrix, Illumina [508849] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081000 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40: Inguinal hernia (Gene-based burden) 19,501 European ancestry cases, 365,524 European ancestry controls NA Illumina [185299] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90084206 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.9: Type 2 diabetes mellitus without complications 26,590 European ancestry cases, 359,248 European ancestry controls 29,149 European ancestry cases, 91,572 European ancestry controls Affymetrix, Illumina [508845] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079741 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40.2: Bilateral inguinal hernia, without obstruction or gangrene (Gene-based burden) 1,780 European ancestry cases, 386,150 European ancestry controls NA Illumina [185344] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90084204 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31.2: Other microscopic hematuria 541 European ancestry cases, 385,315 European ancestry controls NA Affymetrix, Illumina [508844] 0 Microscopic hematuria http://purl.obolibrary.org/obo/HP_0002907 GCST90080840 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40.9: Unilateral inguinal hernia, without obstruction or gangrene (Gene-based burden) 16,831 European ancestry cases, 371,091 European ancestry controls NA Illumina [185344] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90084205 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31.29: Other microscopic hematuria 541 European ancestry cases, 385,315 European ancestry controls NA Affymetrix, Illumina [508844] 0 Microscopic hematuria http://purl.obolibrary.org/obo/HP_0002907 GCST90080839 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K41: Femoral hernia (Gene-based burden) 806 European ancestry cases, 386,955 European ancestry controls NA Illumina [185343] 0 femoral hernia http://www.ebi.ac.uk/efo/EFO_1001791 GCST90084208 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W54: Contact with dog 892 European ancestry cases, 385,017 European ancestry controls NA Affymetrix, Illumina [508842] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081130 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K41.9: Unilateral femoral hernia, without obstruction or gangrene (Gene-based burden) 629 European ancestry cases, 387,301 European ancestry controls NA Illumina [185344] 0 femoral hernia http://www.ebi.ac.uk/efo/EFO_1001791 GCST90084207 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.31: Type 2 diabetes mellitus with unspecified diabetic retinopathy 2,622 European ancestry cases, 383,255 European ancestry controls NA Affymetrix, Illumina [508828] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079735 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K42: Umbilical hernia (Gene-based burden) 4,830 European ancestry cases, 382,071 European ancestry controls NA Illumina [185318] 0 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90084210 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63: Other diseases of intestine 19,547 European ancestry cases, 366,223 European ancestry controls NA Affymetrix, Illumina [508822] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080274 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K42.9: Umbilical hernia without obstruction or gangrene (Gene-based burden) 4,355 European ancestry cases, 383,572 European ancestry controls NA Illumina [185344] 0 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90084209 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G25: Other extrapyramidal and movement disorders 1,721 European ancestry cases, 384,069 European ancestry controls NA Affymetrix, Illumina [508821] 0 movement disorder http://www.ebi.ac.uk/efo/EFO_0004280 GCST90079818 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K43: Ventral hernia (Gene-based burden) 4,359 European ancestry cases, 382,701 European ancestry controls NA Illumina [185329] 0 ventral hernia http://www.ebi.ac.uk/efo/EFO_1001866 GCST90084212 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20.8: Other disturbances of skin sensation 3,285 European ancestry cases, 382,547 European ancestry controls NA Affymetrix, Illumina [508818] 0 disturbance of skin sensation http://www.ebi.ac.uk/efo/EFO_0009522 GCST90080816 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K43.9: Ventral hernia without obstruction or gangrene (Gene-based burden) 3,779 European ancestry cases, 384,151 European ancestry controls NA Illumina [185344] 0 ventral hernia http://www.ebi.ac.uk/efo/EFO_1001866 GCST90084211 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G45: Transient cerebral ischemic attacks and related syndromes 4,034 European ancestry cases, 381,709 European ancestry controls NA Affymetrix, Illumina [508812] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90079830 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K44: Diaphragmatic hernia (Gene-based burden) 34,622 European ancestry cases, 350,249 European ancestry controls NA Illumina [185299] 0 diaphragmatic hernia http://www.ebi.ac.uk/efo/EFO_0008561 GCST90084214 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08.89: Other specified local infections of the skin and subcutaneous tissue 716 European ancestry cases, 385,049 European ancestry controls NA Affymetrix, Illumina [508812] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080333 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83: Family history of other specific disorders 4,125 European ancestry cases, 372,628 European ancestry controls 8,889 European ancestry cases, 33,304 European ancestry controls Affymetrix, Illumina [500600] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081343 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.0: Endometriosis of uterus (Gene-based burden) 2,024 European ancestry cases, 227,110 European ancestry controls NA Illumina [180826] 0 adenomyosis http://purl.obolibrary.org/obo/MONDO_0010888 GCST90084634 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B34: Viral infection of unspecified site 4,826 European ancestry cases, 371,590 European ancestry controls NA Affymetrix, Illumina [500532] 0 viral disease http://www.ebi.ac.uk/efo/EFO_0000763 GCST90079552 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.1: Endometriosis of ovary (Gene-based burden) 1,042 European ancestry cases, 228,092 European ancestry controls NA Illumina [180826] 0 Ovarian Endometriosis http://www.ebi.ac.uk/efo/EFO_1000418 GCST90084635 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism / Pulmonary embolism 5,226 European ancestry cases, 371,230 European ancestry controls 3,467 European ancestry cases, 117,976 European ancestry controls Affymetrix, Illumina [500506] 0 venous thromboembolism, pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0004286, http://www.ebi.ac.uk/efo/EFO_0003827 GCST90081536 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.3: Endometriosis of pelvic peritoneum (Gene-based burden) 811 European ancestry cases, 228,323 European ancestry controls NA Illumina [180825] 0 endometriosis of pelvic peritoneum http://purl.obolibrary.org/obo/MONDO_0001285 GCST90084636 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma strict 39,436 European ancestry cases, 336,853 European ancestry controls NA Affymetrix, Illumina [500428] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081460 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N80.9: Endometriosis, unspecified (Gene-based burden) 840 European ancestry cases, 210,931 European ancestry controls NA Illumina [179932] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90084637 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Apolipoprotein A levels (UKB data field 30630) 376,129 European ancestry individuals NA Affymetrix, Illumina [500358] 14 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90079016 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81: Female genital prolapse (Gene-based burden) 14,361 European ancestry cases, 194,168 European ancestry controls NA Illumina [179696] 0 uterine prolapse http://www.ebi.ac.uk/efo/EFO_1001864 GCST90084644 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94: Abnormal results of function studies 8,623 European ancestry cases, 367,496 European ancestry controls NA Affymetrix, Illumina [500349] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90080937 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.1: Cystocele (Gene-based burden) 5,753 European ancestry cases, 205,179 European ancestry controls NA Illumina [179871] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084639 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M72: Fibroblastic disorders 8,539 European ancestry cases, 367,694 European ancestry controls NA Affymetrix, Illumina [500286] 0 fibroblastic disorder http://www.ebi.ac.uk/efo/EFO_0009432 GCST90080531 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.2: Incomplete uterovaginal prolapse (Gene-based burden) 4,359 European ancestry cases, 207,635 European ancestry controls NA Illumina [179941] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084640 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88: Allergy status to drugs, medicaments and biological substances 36,339 European ancestry cases, 339,428 European ancestry controls NA Affymetrix, Illumina [500110] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081388 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.4: Uterovaginal prolapse, unspecified (Gene-based burden) 1,373 European ancestry cases, 227,761 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084641 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H57.9: Unspecified disorder of eye and adnexa 3,361 European ancestry cases, 372,277 European ancestry controls NA Affymetrix, Illumina [499935] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079925 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.5: Vaginal enterocele (Gene-based burden) 789 European ancestry cases, 228,345 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084642 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.618.: Other abnormal cytological findings on specimens from cervix uteri 6,536 European ancestry cases, 369,132 European ancestry controls NA Affymetrix, Illumina [499894] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080920 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N81.6: Rectocele (Gene-based burden) 5,126 European ancestry cases, 206,385 European ancestry controls NA Illumina [179915] 0 rectocele http://www.ebi.ac.uk/efo/EFO_1001837 GCST90084643 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B02: Zoster [herpes zoster] 2,991 European ancestry cases, 372,592 European ancestry controls NA Affymetrix, Illumina [499853] 0 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST90079549 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83: Noninflammatory disorders of ovary, fallopian tube and broad ligament (Gene-based burden) 6,167 European ancestry cases, 203,364 European ancestry controls NA Illumina [179792] 0 fallopian tube disease http://www.ebi.ac.uk/efo/EFO_0009548 GCST90084649 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.2: Person consulting for explanation of examination or test findings 11,120 European ancestry cases, 364,626 European ancestry controls NA Affymetrix, Illumina [499848] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081305 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.0: Follicular cyst of ovary (Gene-based burden) 574 European ancestry cases, 228,560 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084645 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01: Encounter for other special examination without complaint, suspected or reported diagnosis 157,424 European ancestry cases, 220,162 European ancestry controls NA Affymetrix, Illumina [501307] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081184 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N52.9: Male erectile dysfunction, unspecified (Gene-based burden) 6,768 European ancestry cases, 372,700 European ancestry controls NA Illumina [185190] 0 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST90084622 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B07: Viral warts 4,761 European ancestry cases, 372,404 European ancestry controls NA Affymetrix, Illumina [501171] 0 common wart http://www.ebi.ac.uk/efo/EFO_0009662 GCST90079550 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N60: Benign mammary dysplasia (Gene-based burden) 3,431 European ancestry cases, 203,229 European ancestry controls NA Illumina [179594] 0 breast fibrocystic disease http://www.ebi.ac.uk/efo/EFO_0003014 GCST90084624 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-alcoholic fatty liver disease - Cirrhosis 852 European ancestry cases, 376,493 European ancestry controls NA Affymetrix, Illumina [501170] 0 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90081500 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N61: Inflammatory disorders of breast (Gene-based burden) 987 European ancestry cases, 208,795 European ancestry controls NA Illumina [179811] 0 mastitis http://www.ebi.ac.uk/efo/EFO_1001034 GCST90084625 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72: Follicular cysts of skin and subcutaneous tissue 12,083 European ancestry cases, 364,969 European ancestry controls 5,880 European ancestry cases, 93,588 European ancestry controls Affymetrix, Illumina [501130] 0 Follicular Cyst http://www.ebi.ac.uk/efo/EFO_1001329 GCST90080364 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N62: Hypertrophy of breast (Gene-based burden) 707 European ancestry cases, 211,231 European ancestry controls NA Illumina [179938] 0 Breast hypertrophy http://purl.obolibrary.org/obo/HP_0010313 GCST90084626 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.2: Cervicalgia 6,608 European ancestry cases, 370,716 European ancestry controls NA Affymetrix, Illumina [501125] 0 Neck pain http://purl.obolibrary.org/obo/HP_0030833 GCST90080502 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N63: Unspecified lump in breast (Gene-based burden) 6,317 European ancestry cases, 195,686 European ancestry controls NA Illumina [179300] 0 breast cyst http://www.ebi.ac.uk/efo/EFO_1000848 GCST90084627 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23: Other benign neoplasms of skin 7,862 European ancestry cases, 369,330 European ancestry controls NA Affymetrix, Illumina [501107] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079683 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N70: Salpingitis and oophoritis (Gene-based burden) 618 European ancestry cases, 211,035 European ancestry controls NA Illumina [179913] 0 Pelvic Inflammatory Disease http://www.ebi.ac.uk/efo/EFO_1001388 GCST90084628 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.0: Tobacco use 21,842 European ancestry cases, 355,170 European ancestry controls 4,963 European ancestry cases, 96,913 European ancestry controls Affymetrix, Illumina [501011] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90081310 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N72: Inflammatory disease of cervix uteri (Gene-based burden) 1,272 European ancestry cases, 210,139 European ancestry controls NA Illumina [179912] 0 Cervicitis http://purl.obolibrary.org/obo/HP_0030160 GCST90084629 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.89: Other chest pain 2,521 European ancestry cases, 374,512 European ancestry controls NA Affymetrix, Illumina [500977] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90080776 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N73: Other female pelvic inflammatory diseases (Gene-based burden) 3,315 European ancestry cases, 207,461 European ancestry controls NA Illumina [179853] 0 Pelvic Inflammatory Disease http://www.ebi.ac.uk/efo/EFO_1001388 GCST90084631 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39: Other and unspecified symptoms and signs involving the genitourinary system 9,404 European ancestry cases, 367,195 European ancestry controls NA Affymetrix, Illumina [500741] 0 Abnormality of the urinary system http://purl.obolibrary.org/obo/HP_0000079 GCST90080852 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N73.6: Female pelvic peritoneal adhesions (postinfective) (Gene-based burden) 2,865 European ancestry cases, 226,269 European ancestry controls NA Illumina [180826] 0 disease of peritoneum http://www.ebi.ac.uk/efo/EFO_0009541 GCST90084630 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.9: Allergy status to unspecified drugs, medicaments and biological substances status 4,483 European ancestry cases, 372,028 European ancestry controls NA Affymetrix, Illumina [500662] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081387 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N75: Diseases of Bartholin's gland (Gene-based burden) 988 European ancestry cases, 209,981 European ancestry controls NA Illumina [179894] 0 Bartholin gland disease http://www.ebi.ac.uk/efo/EFO_0009469 GCST90084632 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32: Chronic sinusitis 6,974 European ancestry cases, 369,561 European ancestry controls NA Affymetrix, Illumina [500626] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90080109 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-06-17 33243845 Strausz S 2020-11-26 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33243845 Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health. Obstructive sleep apnea 16,761 Finnish ancestry cases, 201,194 Finnish ancestry controls 10,348 European or unknown ancestry cases, 474,608 European or unknown ancestry controls Affymetrix, Illumina [NR] (imputed) 1 obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0003918 GCST011922 Genome-wide genotyping array 2021-06-17 33243845 Strausz S 2020-11-26 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/33243845 Genetic analysis of obstructive sleep apnoea discovers a strong association with cardiometabolic health. Obstructive sleep apnea (BMI adjusted) 12,759 Finnish ancestry cases, 146,972 Finnish ancestry controls NR Affymetrix, Illumina [NR] (imputed) 2 obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0003918 GCST011921 Genome-wide genotyping array 2021-09-06 33852427 Wittekind DA 2021-04-01 Eur J Endocrinol www.ncbi.nlm.nih.gov/pubmed/33852427 Genome-wide association and transcriptome analysis suggests total serum ghrelin to be linked with GFRAL. ghrelin levels 1,501 individuals NA Affymetrix [9868623] (imputed) 13 ghrelin measurement http://www.ebi.ac.uk/efo/EFO_0600001 GCST012316 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.3: Fracture of other and unspecified metacarpal bone 736 European ancestry cases, 384,858 European ancestry controls NA Affymetrix, Illumina [508712] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080999 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.2: Volvulus (Gene-based burden) 828 European ancestry cases, 387,086 European ancestry controls NA Illumina [185344] 0 Gastrointestinal obstruction http://purl.obolibrary.org/obo/HP_0004796 GCST90084226 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S92.3: Fracture of metatarsal bone(s) 710 European ancestry cases, 384,817 European ancestry controls NA Affymetrix, Illumina [508698] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90081038 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.5: Intestinal adhesions [bands] with obstruction (postinfection) (Gene-based burden) 1,110 European ancestry cases, 386,820 European ancestry controls NA Illumina [185344] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084227 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K13: Other diseases of lip and oral mucosa 3,921 European ancestry cases, 381,774 European ancestry controls NA Affymetrix, Illumina [508694] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90080182 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.6: Other and unspecified intestinal obstruction (Gene-based burden) 2,586 European ancestry cases, 385,172 European ancestry controls NA Illumina [185344] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084228 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S39: Other and unspecified injuries of abdomen, lower back, pelvis and external genitals 574 European ancestry cases, 385,098 European ancestry controls NA Affymetrix, Illumina [508682] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080973 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.7: Ileus, unspecified (Gene-based burden) 590 European ancestry cases, 387,340 European ancestry controls NA Illumina [185344] 0 ileus http://purl.obolibrary.org/obo/MONDO_0004567 GCST90084229 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R23.8: Other skin changes 598 European ancestry cases, 385,129 European ancestry controls NA Affymetrix, Illumina [508673] 0 Abnormality of the skin http://purl.obolibrary.org/obo/HP_0000951 GCST90080824 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57: Diverticular disease of intestine (Gene-based burden) 37,004 European ancestry cases, 347,630 European ancestry controls NA Illumina [185289] 0 diverticulitis http://www.ebi.ac.uk/efo/EFO_1001460 GCST90084235 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.7: Acquired absence of genital organ(s) 7,830 European ancestry cases, 377,764 European ancestry controls NA Affymetrix, Illumina [508628] 0 organ extraction http://www.ebi.ac.uk/efo/EFO_0009124 GCST90081394 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.1: Diverticular disease of small intestine without perforation or abscess (Gene-based burden) 510 European ancestry cases, 387,411 European ancestry controls NA Illumina [185344] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084231 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76: Other diseases of liver 5,337 European ancestry cases, 380,284 European ancestry controls NA Affymetrix, Illumina [508617] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90080292 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.2: Diverticulitis of large intestine with perforation and abscess (Gene-based burden) 623 European ancestry cases, 387,299 European ancestry controls NA Illumina [185344] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084232 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90: Acquired absence of organs, not elsewhere classified 20,599 European ancestry cases, 364,959 European ancestry controls 8,986 European ancestry cases, 33,208 European ancestry controls Affymetrix, Illumina [508614] 0 organ extraction http://www.ebi.ac.uk/efo/EFO_0009124 GCST90081395 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.3: Diverticular disease of large intestine without perforation or abscess (Gene-based burden) 31,734 European ancestry cases, 356,184 European ancestry controls NA Illumina [185344] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084233 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M94: Other disorders of cartilage 1,122 European ancestry cases, 384,496 European ancestry controls NA Affymetrix, Illumina [508607] 0 cartilage disease http://www.ebi.ac.uk/efo/EFO_0005802 GCST90080568 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.9: Diverticular disease of intestine, part unspecified, without perforation or abscess (Gene-based burden) 8,627 European ancestry cases, 378,304 European ancestry controls NA Illumina [185323] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084234 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.0: Family history of malignant neoplasm of digestive organs 9,455 European ancestry cases, 376,016 European ancestry controls 5,370 European ancestry cases, 33,532 European ancestry controls Affymetrix, Illumina [508605] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90081329 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58: Irritable bowel syndrome (Gene-based burden) 11,224 European ancestry cases, 366,402 European ancestry controls NA Illumina [185187] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90084238 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.02: Impaired glucose tolerance (oral) 712 European ancestry cases, 384,821 European ancestry controls NA Affymetrix, Illumina [508595] 0 abnormal glucose tolerance http://www.ebi.ac.uk/efo/EFO_0002546 GCST90080902 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58.0: Irritable bowel syndrome with diarrhea (Gene-based burden) 543 European ancestry cases, 387,387 European ancestry controls NA Illumina [185344] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90084236 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08.8: Other specified local infections of the skin and subcutaneous tissue 973 European ancestry cases, 384,549 European ancestry controls NA Affymetrix, Illumina [508578] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080334 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58.9: Irritable bowel syndrome without diarrhea (Gene-based burden) 6,678 European ancestry cases, 381,252 European ancestry controls NA Illumina [185344] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90084237 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M67.4: Ganglion 3,644 European ancestry cases, 381,796 European ancestry controls NA Affymetrix, Illumina [508571] 0 ganglion http://purl.obolibrary.org/obo/UBERON_0000045 GCST90080522 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.8: Other chest pain 2,766 European ancestry cases, 372,667 European ancestry controls NA Affymetrix, Illumina [499626] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90080777 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84.1: Polyp of cervix uteri (Gene-based burden) 3,637 European ancestry cases, 207,539 European ancestry controls NA Illumina [179898] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90084651 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma 61,807 European ancestry cases, 313,658 European ancestry controls NA Affymetrix, Illumina [499603] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081461 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.0: Endometrial hyperplasia (Gene-based burden) 1,071 European ancestry cases, 210,928 European ancestry controls NA Illumina [179937] 0 obsolete endometrial hyperplasia http://purl.obolibrary.org/obo/MONDO_0041161 GCST90084653 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.2: Nicotine dependence 5,766 European ancestry cases, 369,408 European ancestry controls NA Affymetrix, Illumina [499540] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90079797 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.2: Hypertrophy of uterus (Gene-based burden) 1,253 European ancestry cases, 227,881 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084654 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.20: Nicotine dependence, unspecified 4,932 European ancestry cases, 370,207 European ancestry controls NA Affymetrix, Illumina [499505] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90079796 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.4: Malposition of uterus (Gene-based burden) 872 European ancestry cases, 211,111 European ancestry controls NA Illumina [179940] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084655 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17.201.: Nicotine dependence, unspecified, in remission 4,932 European ancestry cases, 370,207 European ancestry controls NA Affymetrix, Illumina [499505] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90079795 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N85.8: Other specified noninflammatory disorders of uterus (Gene-based burden) 2,734 European ancestry cases, 209,232 European ancestry controls NA Illumina [179939] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084656 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R68.8: Other general symptoms and signs 4,834 European ancestry cases, 370,577 European ancestry controls NA Affymetrix, Illumina [499395] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90080898 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N86: Erosion and ectropion of cervix uteri (Gene-based burden) 1,108 European ancestry cases, 209,282 European ancestry controls NA Illumina [179818] 0 cervix erosion http://www.ebi.ac.uk/efo/EFO_1000862 GCST90084657 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.8: Encounter for screening for other specified diseases and disorders 8,520 European ancestry cases, 366,567 European ancestry controls NA Affymetrix, Illumina [499385] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081218 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N87: Dysplasia of cervix uteri (Gene-based burden) 3,148 European ancestry cases, 205,857 European ancestry controls NA Illumina [179741] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90084660 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R68.89: Other general symptoms and signs 4,075 European ancestry cases, 371,328 European ancestry controls NA Affymetrix, Illumina [499382] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90080897 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N87.0: Mild cervical dysplasia (Gene-based burden) 665 European ancestry cases, 211,333 European ancestry controls NA Illumina [179941] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90084658 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R68: Other general symptoms and signs 5,024 European ancestry cases, 370,295 European ancestry controls NA Affymetrix, Illumina [499318] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90080899 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N87.9: Dysplasia of cervix uteri, unspecified (Gene-based burden) 527 European ancestry cases, 211,441 European ancestry controls NA Illumina [179941] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90084659 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sex hormone binding globulin levels (UKB data field 30830) 374,810 European ancestry individuals 5,908 European ancestry individuals Affymetrix, Illumina [499310] 1 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90079040 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N88: Other noninflammatory disorders of cervix uteri (Gene-based burden) 2,098 European ancestry cases, 209,410 European ancestry controls NA Illumina [179905] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084663 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47: Sleep disorders 11,129 European ancestry cases, 364,046 European ancestry controls NA Affymetrix, Illumina [499175] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90079835 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N88.2: Stricture and stenosis of cervix uteri (Gene-based burden) 789 European ancestry cases, 228,345 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084661 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.89: Personal history of other specified conditions 48,740 European ancestry cases, 326,162 European ancestry controls NA Affymetrix, Illumina [499141] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081378 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N88.8: Other specified noninflammatory disorders of cervix uteri (Gene-based burden) 1,130 European ancestry cases, 210,838 European ancestry controls NA Illumina [179938] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084662 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75: Shoulder lesions 16,150 European ancestry cases, 358,370 European ancestry controls NA Affymetrix, Illumina [498905] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080537 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59: Other functional intestinal disorders (Gene-based burden) 18,263 European ancestry cases, 359,286 European ancestry controls NA Illumina [185162] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084241 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18: Pneumonia, unspecified organism 13,681 European ancestry cases, 371,904 European ancestry controls NA Affymetrix, Illumina [508569] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90080098 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59.0: Constipation (Gene-based burden) 16,745 European ancestry cases, 363,304 European ancestry controls NA Illumina [185208] 0 constipation disorder http://purl.obolibrary.org/obo/MONDO_0002203 GCST90084240 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M84: Disorder of continuity of bone 2,120 European ancestry cases, 383,442 European ancestry controls NA Affymetrix, Illumina [508568] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90080561 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59.00: Constipation, unspecified (Gene-based burden) 3,370 European ancestry cases, 375,690 European ancestry controls NA Illumina [185183] 0 constipation disorder http://purl.obolibrary.org/obo/MONDO_0002203 GCST90084239 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.2: Dependence on renal dialysis 1,868 European ancestry cases, 383,685 European ancestry controls 917 European ancestry cases, 34,705 European ancestry controls Affymetrix, Illumina [508562] 0 renal dialysis http://www.ebi.ac.uk/efo/EFO_0010690 GCST90081442 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60: Fissure and fistula of anal and rectal regions (Gene-based burden) 4,446 European ancestry cases, 379,680 European ancestry controls NA Illumina [185288] 0 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90084245 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E55.9: Vitamin D deficiency, unspecified 1,372 European ancestry cases, 384,186 European ancestry controls NA Affymetrix, Illumina [508558] 0 vitamin D deficiency http://www.ebi.ac.uk/efo/EFO_0003762 GCST90079759 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60.1: Chronic anal fissure (Gene-based burden) 577 European ancestry cases, 387,353 European ancestry controls NA Illumina [185344] 0 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90084242 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92: Other diseases of digestive system 12,732 European ancestry cases, 372,840 European ancestry controls NA Affymetrix, Illumina [508556] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080322 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60.2: Anal fissure, unspecified (Gene-based burden) 1,863 European ancestry cases, 386,067 European ancestry controls NA Illumina [185344] 0 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90084243 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N23: Unspecified renal colic 2,723 European ancestry cases, 382,722 European ancestry controls NA Affymetrix, Illumina [508546] 0 renal colic http://www.ebi.ac.uk/efo/EFO_1001412 GCST90080591 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60.3: Anal fistula (Gene-based burden) 1,370 European ancestry cases, 386,560 European ancestry controls NA Illumina [185344] 0 Anal fistula http://purl.obolibrary.org/obo/HP_0010447 GCST90084244 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.1: Alcohol abuse 4,296 European ancestry cases, 381,055 European ancestry controls NA Affymetrix, Illumina [508536] 0 alcohol abuse http://purl.obolibrary.org/obo/MONDO_0002046 GCST90079789 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K61: Abscess of anal and rectal regions (Gene-based burden) 1,733 European ancestry cases, 385,413 European ancestry controls NA Illumina [185331] 0 Rectal abscess http://purl.obolibrary.org/obo/HP_0005224 GCST90084247 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78.00: Pure hypercholesterolemia, unspecified 5,498 European ancestry cases, 369,901 European ancestry controls NA Affymetrix, Illumina [499742] 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90079765 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.1: Corpus luteum cyst (Gene-based burden) 540 European ancestry cases, 228,594 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084646 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N31: Neuromuscular dysfunction of bladder, not elsewhere classified 2,404 European ancestry cases, 383,356 European ancestry controls NA Affymetrix, Illumina [508791] 0 Neurogenic bladder http://purl.obolibrary.org/obo/HP_0000011 GCST90080602 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K51: Ulcerative colitis (Gene-based burden) 3,928 European ancestry cases, 383,552 European ancestry controls NA Illumina [185340] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90084220 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.2: Procedure and treatment not carried out because of patient's decision for other and unspecified reasons 2,380 European ancestry cases, 383,365 European ancestry controls NA Affymetrix, Illumina [508781] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081289 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K51.9: Ulcerative colitis, unspecified (Gene-based burden) 3,242 European ancestry cases, 384,687 European ancestry controls NA Illumina [185344] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90084219 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.3: Abnormal sputum 578 European ancestry cases, 385,258 European ancestry controls NA Affymetrix, Illumina [508778] 0 Abnormal sputum http://purl.obolibrary.org/obo/HP_0032016 GCST90080781 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52: Other and unspecified noninfective gastroenteritis and colitis (Gene-based burden) 19,104 European ancestry cases, 362,399 European ancestry controls NA Illumina [185263] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90084223 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I49: Other cardiac arrhythmias 4,054 European ancestry cases, 381,711 European ancestry controls NA Affymetrix, Illumina [508760] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90080019 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52.8: Other specified noninfective gastroenteritis and colitis (Gene-based burden) 650 European ancestry cases, 387,279 European ancestry controls NA Illumina [185344] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90084221 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.9: Other and unspecified asthma 38,114 European ancestry cases, 347,640 European ancestry controls 17,224 European ancestry cases, 90,352 European ancestry controls Affymetrix, Illumina [508756] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90080140 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52.9: Noninfective gastroenteritis and colitis, unspecified (Gene-based burden) 17,883 European ancestry cases, 365,747 European ancestry controls NA Illumina [185291] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90084222 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L73.9: Follicular disorder, unspecified 680 European ancestry cases, 384,976 European ancestry controls NA Affymetrix, Illumina [508748] 0 folliculitis http://www.ebi.ac.uk/efo/EFO_1000702 GCST90080365 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K55: Vascular disorders of intestine (Gene-based burden) 1,491 European ancestry cases, 386,337 European ancestry controls NA Illumina [185344] 0 vascular disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0004264, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084225 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F45: Somatoform disorders 844 European ancestry cases, 384,989 European ancestry controls NA Affymetrix, Illumina [508737] 0 somatoform disorder http://www.ebi.ac.uk/efo/EFO_0009687 GCST90079814 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K55.2: Angiodysplasia of colon (Gene-based burden) 619 European ancestry cases, 387,311 European ancestry controls NA Illumina [185344] 0 Gastrointestinal angiodysplasia http://purl.obolibrary.org/obo/HP_0000471 GCST90084224 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.7: Gastritis, unspecified 19,439 European ancestry cases, 366,238 European ancestry controls NA Affymetrix, Illumina [508721] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90080206 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56: Paralytic ileus and intestinal obstruction without hernia (Gene-based burden) 5,258 European ancestry cases, 382,088 European ancestry controls NA Illumina [185340] 0 Gastrointestinal obstruction http://purl.obolibrary.org/obo/HP_0004796 GCST90084230 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.891.: Personal history of nicotine dependence 48,661 European ancestry cases, 326,806 European ancestry controls NA Affymetrix, Illumina [499676] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90081377 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.2: Other and unspecified ovarian cysts (Gene-based burden) 4,400 European ancestry cases, 206,584 European ancestry controls NA Illumina [179876] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084647 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20: Disturbances of skin sensation 7,669 European ancestry cases, 367,888 European ancestry controls NA Affymetrix, Illumina [499669] 0 disturbance of skin sensation http://www.ebi.ac.uk/efo/EFO_0009522 GCST90080817 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N83.8: Other noninflammatory disorders of ovary, fallopian tube and broad ligament (Gene-based burden) 611 European ancestry cases, 211,393 European ancestry controls NA Illumina [179941] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084648 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R52: Pain, unspecified 6,438 European ancestry cases, 369,102 European ancestry controls NA Affymetrix, Illumina [499653] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90080873 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84: Polyp of female genital tract (Gene-based burden) 12,343 European ancestry cases, 197,217 European ancestry controls NA Illumina [179807] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90084652 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H92: Otalgia and effusion of ear 4,717 European ancestry cases, 370,723 European ancestry controls NA Affymetrix, Illumina [499628] 0 Ear pain, otitis media with effusion http://purl.obolibrary.org/obo/HP_0030766, http://www.ebi.ac.uk/efo/EFO_0007415 GCST90079952 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N84.0: Polyp of corpus uteri (Gene-based burden) 8,912 European ancestry cases, 203,081 European ancestry controls NA Illumina [179940] 0 female genital tract polyp http://www.ebi.ac.uk/efo/EFO_0008622 GCST90084650 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K44.9: Diaphragmatic hernia without obstruction or gangrene (Gene-based burden) 34,283 European ancestry cases, 352,048 European ancestry controls NA Illumina [185333] 0 diaphragmatic hernia http://www.ebi.ac.uk/efo/EFO_0008561 GCST90084213 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.30: Unspecified fracture of other metacarpal bone 613 European ancestry cases, 385,091 European ancestry controls NA Affymetrix, Illumina [508806] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080998 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K46: Unspecified abdominal hernia (Gene-based burden) 730 European ancestry cases, 385,509 European ancestry controls NA Illumina [185324] 0 Hernia of the abdominal wall http://purl.obolibrary.org/obo/HP_0004299 GCST90084215 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z02.9: Encounter for administrative examinations, unspecified 2,204 European ancestry cases, 383,513 European ancestry controls NA Affymetrix, Illumina [508804] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081186 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50: Crohn's disease [regional enteritis] (Gene-based burden) 2,106 European ancestry cases, 385,486 European ancestry controls NA Illumina [185338] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90084218 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.09: Procedure and treatment not carried out because of other contraindication 1,754 European ancestry cases, 383,927 European ancestry controls NA Affymetrix, Illumina [508803] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081287 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50.1: Crohn's disease of large intestine (Gene-based burden) 591 European ancestry cases, 387,339 European ancestry controls NA Illumina [185344] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90084216 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.0: Fracture of clavicle 1,184 European ancestry cases, 384,507 European ancestry controls NA Affymetrix, Illumina [508799] 0 clavicle fracture http://www.ebi.ac.uk/efo/EFO_0009614 GCST90080975 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50.9: Crohn's disease, unspecified (Gene-based burden) 1,697 European ancestry cases, 386,228 European ancestry controls NA Illumina [185344] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90084217 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K40: Inguinal hernia 19,501 European ancestry cases, 365,524 European ancestry controls NA Affymetrix, Illumina [508134] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90080220 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83: Other diseases of biliary tract (Gene-based burden) 2,749 European ancestry cases, 384,669 European ancestry controls NA Illumina [185335] 0 biliary tract disease http://www.ebi.ac.uk/efo/EFO_0009534 GCST90084294 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73: Other peripheral vascular diseases 5,786 European ancestry cases, 379,242 European ancestry controls NA Affymetrix, Illumina [508128] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90080051 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83.0: Cholangitis (Gene-based burden) 750 European ancestry cases, 387,180 European ancestry controls NA Illumina [185344] 0 Cholangitis http://purl.obolibrary.org/obo/HP_0030151 GCST90084291 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S09.92: Unspecified injury of nose 657 European ancestry cases, 384,430 European ancestry controls NA Affymetrix, Illumina [508126] 0 nose injury http://www.ebi.ac.uk/efo/EFO_0009623 GCST90080953 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83.1: Obstruction of bile duct (Gene-based burden) 1,070 European ancestry cases, 386,859 European ancestry controls NA Illumina [185344] 0 cholestasis http://purl.obolibrary.org/obo/MONDO_0001751 GCST90084292 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A08: Viral and other specified intestinal infections 1,306 European ancestry cases, 383,755 European ancestry controls NA Affymetrix, Illumina [508123] 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90079541 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83.8: Other specified diseases of biliary tract (Gene-based burden) 1,262 European ancestry cases, 386,668 European ancestry controls NA Illumina [185344] 0 biliary tract disease http://www.ebi.ac.uk/efo/EFO_0009534 GCST90084293 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S43: Dislocation and sprain of joints and ligaments of shoulder girdle 962 European ancestry cases, 384,037 European ancestry controls NA Affymetrix, Illumina [508122] 0 dislocation, sprain http://www.ebi.ac.uk/efo/EFO_0009521, http://www.ebi.ac.uk/efo/EFO_0009582 GCST90080982 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K85: Acute pancreatitis (Gene-based burden) 2,460 European ancestry cases, 385,091 European ancestry controls NA Illumina [185339] 0 acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1000652 GCST90084296 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.2: Wheezing 1,393 European ancestry cases, 383,622 European ancestry controls NA Affymetrix, Illumina [508112] 0 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90080768 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K85.9: Acute pancreatitis, unspecified (Gene-based burden) 708 European ancestry cases, 387,020 European ancestry controls NA Illumina [185341] 0 acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1000652 GCST90084295 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.2: Personal history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism 866 European ancestry cases, 384,120 European ancestry controls NA Affymetrix, Illumina [508109] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081357 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K86: Other diseases of pancreas (Gene-based burden) 1,601 European ancestry cases, 386,179 European ancestry controls NA Illumina [185343] 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90084299 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M15: Polyosteoarthritis 6,260 European ancestry cases, 378,716 European ancestry controls NA Affymetrix, Illumina [508093] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080408 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K86.1: Other chronic pancreatitis (Gene-based burden) 535 European ancestry cases, 387,394 European ancestry controls NA Illumina [185344] 0 chronic pancreatitis http://www.ebi.ac.uk/efo/EFO_0000342 GCST90084297 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17.9: Osteoarthritis of knee, unspecified 20,719 European ancestry cases, 364,237 European ancestry controls NA Affymetrix, Illumina [508071] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90080415 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K86.8: Other specified diseases of pancreas (Gene-based burden) 582 European ancestry cases, 387,348 European ancestry controls NA Illumina [185344] 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90084298 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R61: Generalized hyperhidrosis 1,491 European ancestry cases, 383,413 European ancestry controls NA Affymetrix, Illumina [508059] 0 Hyperhidrosis http://purl.obolibrary.org/obo/HP_0000975 GCST90080892 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K90: Intestinal malabsorption (Gene-based burden) 2,759 European ancestry cases, 384,510 European ancestry controls NA Illumina [185338] 0 malabsorption syndrome http://www.ebi.ac.uk/efo/EFO_0009554 GCST90084301 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.149.88: Postprocedural shock 16,135 European ancestry cases, 368,843 European ancestry controls NA Affymetrix, Illumina [508046] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081069 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K90.0: Celiac disease (Gene-based burden) 2,213 European ancestry cases, 385,716 European ancestry controls NA Illumina [185344] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90084300 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E55: Vitamin D deficiency 1,437 European ancestry cases, 383,546 European ancestry controls NA Affymetrix, Illumina [508016] 0 vitamin D deficiency http://www.ebi.ac.uk/efo/EFO_0003762 GCST90079760 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K91: Intraoperative and postprocedural complications and disorders of digestive system, not elsewhere classified (Gene-based burden) 2,050 European ancestry cases, 385,784 European ancestry controls NA Illumina [185340] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084304 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.90: Unspecified asthma 16,105 European ancestry cases, 368,789 European ancestry controls NA Affymetrix, Illumina [508012] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90080137 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K91.4: Colostomy and enterostomy malfunction (Gene-based burden) 635 European ancestry cases, 387,295 European ancestry controls NA Illumina [185344] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084302 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R14.0: Abdominal distension (gaseous) 782 European ancestry cases, 384,049 European ancestry controls NA Affymetrix, Illumina [508010] 0 flatulence http://www.ebi.ac.uk/efo/EFO_0009669 GCST90080801 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K91.8: Other intraoperative and postprocedural complications and disorders of digestive system (Gene-based burden) 962 European ancestry cases, 386,959 European ancestry controls NA Illumina [185343] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084303 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56.6: Other physical and mental strain related to work 1,484 European ancestry cases, 383,319 European ancestry controls NA Affymetrix, Illumina [507997] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081293 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92: Other diseases of digestive system (Gene-based burden) 12,732 European ancestry cases, 372,840 European ancestry controls NA Illumina [185296] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084308 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02: Other disorders of eyelid 7,325 European ancestry cases, 377,441 European ancestry controls NA Affymetrix, Illumina [507979] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90079874 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92.0: Hematemesis (Gene-based burden) 2,304 European ancestry cases, 385,588 European ancestry controls NA Illumina [185339] 0 Hematemesis http://purl.obolibrary.org/obo/HP_0002248 GCST90084305 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K44: Diaphragmatic hernia 34,622 European ancestry cases, 350,249 European ancestry controls NA Affymetrix, Illumina [507978] 0 diaphragmatic hernia http://www.ebi.ac.uk/efo/EFO_0008561 GCST90080228 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92.1: Melena (Gene-based burden) 3,226 European ancestry cases, 384,649 European ancestry controls NA Illumina [185344] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084306 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.49: Other urogenital candidiasis 512 European ancestry cases, 384,170 European ancestry controls NA Affymetrix, Illumina [507939] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90079557 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92.2: Gastrointestinal hemorrhage, unspecified (Gene-based burden) 7,799 European ancestry cases, 380,066 European ancestry controls NA Illumina [185342] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084307 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D64: Other anemias 15,647 European ancestry cases, 369,231 European ancestry controls 24,194 European ancestry cases, 87,619 European ancestry controls Affymetrix, Illumina [507936] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90079712 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L01: Impetigo (Gene-based burden) 591 European ancestry cases, 384,013 European ancestry controls NA Illumina [185266] 0 impetigo http://www.ebi.ac.uk/efo/EFO_1000714 GCST90084309 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94.5: Abnormal results of liver function studies 5,893 European ancestry cases, 378,855 European ancestry controls NA Affymetrix, Illumina [507918] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90080936 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L02: Cutaneous abscess, furuncle and carbuncle (Gene-based burden) 4,703 European ancestry cases, 375,791 European ancestry controls NA Illumina [185238] 0 Cutaneous abscess http://purl.obolibrary.org/obo/HP_0031292 GCST90084312 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.5: Fracture of lower end of radius 5,267 European ancestry cases, 379,424 European ancestry controls NA Affymetrix, Illumina [507890] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080988 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L02.2: Cutaneous abscess, furuncle and carbuncle of trunk (Gene-based burden) 1,025 European ancestry cases, 386,749 European ancestry controls NA Illumina [185344] 0 Cutaneous abscess http://purl.obolibrary.org/obo/HP_0031292 GCST90084310 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S63: Dislocation and sprain of joints and ligaments at wrist and hand level 980 European ancestry cases, 383,792 European ancestry controls NA Affymetrix, Illumina [507877] 0 dislocation, sprain http://www.ebi.ac.uk/efo/EFO_0009521, http://www.ebi.ac.uk/efo/EFO_0009582 GCST90081003 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L02.4: Cutaneous abscess, furuncle and carbuncle of limb (Gene-based burden) 1,320 European ancestry cases, 385,927 European ancestry controls NA Illumina [185336] 0 Cutaneous abscess http://purl.obolibrary.org/obo/HP_0031292 GCST90084311 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J40: Bronchitis, not specified as acute or chronic 1,447 European ancestry cases, 383,299 European ancestry controls NA Affymetrix, Illumina [507873] 0 bronchitis http://www.ebi.ac.uk/efo/EFO_0009661 GCST90080125 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03: Cellulitis and acute lymphangitis (Gene-based burden) 12,973 European ancestry cases, 361,040 European ancestry controls NA Illumina [185133] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90084317 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.10: Vomiting, unspecified 595 European ancestry cases, 384,080 European ancestry controls NA Affymetrix, Illumina [507873] 0 Vomiting http://purl.obolibrary.org/obo/HP_0002013 GCST90080795 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.0: Cellulitis and acute lymphangitis of finger and toe (Gene-based burden) 692 European ancestry cases, 387,237 European ancestry controls NA Illumina [185344] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90084313 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R92.8: Other abnormal and inconclusive findings on diagnostic imaging of breast 870 European ancestry cases, 383,723 European ancestry controls NA Affymetrix, Illumina [507873] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080928 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.1: Cellulitis and acute lymphangitis of other parts of limb (Gene-based burden) 7,078 European ancestry cases, 380,220 European ancestry controls NA Illumina [185335] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90084314 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K65.0: Generalized (acute) peritonitis (Gene-based burden) 598 European ancestry cases, 387,332 European ancestry controls NA Illumina [185344] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90084264 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H66.90: Otitis media, unspecified, unspecified ear 553 European ancestry cases, 384,666 European ancestry controls NA Affymetrix, Illumina [508360] 0 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST90079933 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K66: Other disorders of peritoneum (Gene-based burden) 4,357 European ancestry cases, 383,442 European ancestry controls NA Illumina [185343] 0 disease of peritoneum http://www.ebi.ac.uk/efo/EFO_0009541 GCST90084267 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11: Type 2 diabetes mellitus 27,324 European ancestry cases, 357,976 European ancestry controls 29,639 European ancestry cases, 91,572 European ancestry controls Affymetrix, Illumina [508347] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079742 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K66.0: Peritoneal adhesions (postprocedural) (postinfection) (Gene-based burden) 4,073 European ancestry cases, 383,849 European ancestry controls NA Illumina [185344] 0 disease of peritoneum http://www.ebi.ac.uk/efo/EFO_0009541 GCST90084266 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.2: Personal history of diseases of the skin and subcutaneous tissue 1,460 European ancestry cases, 383,809 European ancestry controls NA Affymetrix, Illumina [508343] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90081369 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K70: Alcoholic liver disease (Gene-based burden) 1,120 European ancestry cases, 386,551 European ancestry controls NA Illumina [185343] 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90084269 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A04: Other bacterial intestinal infections 3,566 European ancestry cases, 381,664 European ancestry controls NA Affymetrix, Illumina [508332] 0 intestinal disease, bacterial disease http://www.ebi.ac.uk/efo/EFO_0009431, http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079539 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K70.9: Alcoholic liver disease, unspecified (Gene-based burden) 709 European ancestry cases, 387,221 European ancestry controls NA Illumina [19298] 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90084268 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L29.0: Pruritus ani 1,392 European ancestry cases, 383,825 European ancestry controls NA Affymetrix, Illumina [508320] 0 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST90080342 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K72: Hepatic failure, not elsewhere classified (Gene-based burden) 566 European ancestry cases, 387,314 European ancestry controls NA Illumina [185344] 0 Hepatic failure http://purl.obolibrary.org/obo/HP_0001399 GCST90084270 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.6: Fracture of other and unspecified finger(s) 1,681 European ancestry cases, 383,442 European ancestry controls NA Affymetrix, Illumina [508319] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081001 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K74: Fibrosis and cirrhosis of liver (Gene-based burden) 1,292 European ancestry cases, 386,463 European ancestry controls NA Illumina [185339] 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90084272 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.79: Other stressful life events affecting family and household 890 European ancestry cases, 384,338 European ancestry controls NA Affymetrix, Illumina [508317] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081301 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K74.6: Other and unspecified cirrhosis of liver (Gene-based burden) 852 European ancestry cases, 387,041 European ancestry controls NA Illumina [185344] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90084271 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K07: Dentofacial anomalies [including malocclusion] 1,054 European ancestry cases, 384,162 European ancestry controls NA Affymetrix, Illumina [508313] 0 Abnormality of the mouth http://purl.obolibrary.org/obo/HP_0000153 GCST90080171 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K75: Other inflammatory liver diseases (Gene-based burden) 965 European ancestry cases, 386,663 European ancestry controls NA Illumina [185341] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90084273 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.83: Snoring 879 European ancestry cases, 384,413 European ancestry controls NA Affymetrix, Illumina [508312] 0 Snoring http://purl.obolibrary.org/obo/HP_0025267 GCST90080770 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76: Other diseases of liver (Gene-based burden) 5,337 European ancestry cases, 380,284 European ancestry controls NA Illumina [185298] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90084278 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.7: Other stressful life events affecting family and household 984 European ancestry cases, 384,233 European ancestry controls NA Affymetrix, Illumina [508304] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081302 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.0: Fatty (change of) liver, not elsewhere classified (Gene-based burden) 2,432 European ancestry cases, 385,498 European ancestry controls NA Illumina [185344] 0 fatty liver disease http://purl.obolibrary.org/obo/MONDO_0004790 GCST90084274 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.30: Lower abdominal pain, unspecified 919 European ancestry cases, 384,254 European ancestry controls NA Affymetrix, Illumina [508303] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90080787 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.6: Portal hypertension (Gene-based burden) 753 European ancestry cases, 387,177 European ancestry controls NA Illumina [185344] 0 portal hypertension http://www.ebi.ac.uk/efo/EFO_0000666 GCST90084275 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94.2: Abnormal results of pulmonary function studies 938 European ancestry cases, 384,331 European ancestry controls NA Affymetrix, Illumina [508289] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90080934 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.8: Other specified diseases of liver (Gene-based burden) 1,267 European ancestry cases, 386,661 European ancestry controls NA Illumina [185344] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90084276 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O02.1: Missed abortion (Gene-based burden) 1,327 European ancestry cases, 210,010 European ancestry controls NA Illumina [179918] 0 abortion http://www.ebi.ac.uk/efo/EFO_1001491 GCST90084689 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Severe depression (UKB data field 20111) 26,143 European ancestry cases, 345,589 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078286 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O03: Spontaneous abortion (Gene-based burden) 2,640 European ancestry cases, 203,668 European ancestry controls NA Illumina [179566] 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90084693 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Prostate cancer (UKB data field 20111) 6,385 European ancestry cases, 365,347 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078287 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O03.4: Incomplete spontaneous abortion without complication (Gene-based burden) 797 European ancestry cases, 211,109 European ancestry controls NA Illumina [179939] 0 incomplete abortion http://www.ebi.ac.uk/efo/EFO_1001799 GCST90084691 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 11 Do not know group 1 (UKB data field 20111) 27,293 European ancestry cases, 344,439 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078296 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O03.9: Complete or unspecified spontaneous abortion without complication (Gene-based burden) 664 European ancestry cases, 211,333 European ancestry controls NA Illumina [179940] 0 abortion http://www.ebi.ac.uk/efo/EFO_1001491 GCST90084692 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 17 None of the above group 1 (UKB data field 20111) 231,453 European ancestry cases, 140,279 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078297 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O13: Gestational [pregnancy-induced] hypertension without significant proteinuria (Gene-based burden) 501 European ancestry cases, 211,311 European ancestry controls NA Illumina [179932] 0 preeclampsia, Proteinuria http://www.ebi.ac.uk/efo/EFO_0000668, http://purl.obolibrary.org/obo/HP_0000093 GCST90084694 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 21 Do not know group 2 (UKB data field 20111) 27,290 European ancestry cases, 344,442 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078298 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O16: Unspecified maternal hypertension (Gene-based burden) 638 European ancestry cases, 211,224 European ancestry controls NA Illumina [179805] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90084695 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - 27 None of the above group 2 (UKB data field 20111) 290,729 European ancestry cases, 81,003 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078299 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O20: Hemorrhage in early pregnancy (Gene-based burden) 1,083 European ancestry cases, 210,227 European ancestry controls NA Illumina [179910] 0 hemorrhage http://purl.obolibrary.org/obo/MP_0001914 GCST90084696 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.56: Pain in knee 11,057 European ancestry cases, 361,984 European ancestry controls NA Affymetrix, Illumina [497392] 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90080457 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O26: Maternal care for other conditions predominantly related to pregnancy (Gene-based burden) 1,939 European ancestry cases, 209,902 European ancestry controls NA Illumina [179932] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084697 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.569.: Pain in unspecified knee 8,703 European ancestry cases, 364,189 European ancestry controls NA Affymetrix, Illumina [497253] 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90080456 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O32: Maternal care for malpresentation of fetus (Gene-based burden) 1,201 European ancestry cases, 210,543 European ancestry controls NA Illumina [179930] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084698 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71.3: Dietary counseling and surveillance 7,443 European ancestry cases, 365,535 European ancestry controls NA Affymetrix, Illumina [497244] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081306 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O34: Maternal care for abnormality of pelvic organs (Gene-based burden) 1,615 European ancestry cases, 210,342 European ancestry controls NA Illumina [179931] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084700 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78: Disorders of lipoprotein metabolism and other lipidemias 51,365 European ancestry cases, 320,834 European ancestry controls 73,057 European ancestry cases, 38,459 European ancestry controls Affymetrix, Illumina [496860] 1 Disorder of amino acid and other organic acid metabolism http://www.orpha.net/ORDO/Orphanet_79062 GCST90079768 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O34.2: Maternal care due to uterine scar from previous surgery (Gene-based burden) 1,286 European ancestry cases, 227,848 European ancestry controls NA Illumina [180640] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084699 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T14.8: Other injury of unspecified body region 3,537 European ancestry cases, 368,536 European ancestry controls NA Affymetrix, Illumina [496802] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081046 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O36: Maternal care for other fetal problems (Gene-based burden) 2,007 European ancestry cases, 209,824 European ancestry controls NA Illumina [179930] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084702 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H60: Otitis externa 10,706 European ancestry cases, 361,578 European ancestry controls NA Affymetrix, Illumina [496745] 0 otitis externa http://www.ebi.ac.uk/efo/EFO_0009560 GCST90079929 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O36.8: Maternal care for other specified fetal problems (Gene-based burden) 1,084 European ancestry cases, 210,917 European ancestry controls NA Illumina [179940] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084701 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93.3: Abnormal findings on diagnostic imaging of other parts of digestive tract 2,213 European ancestry cases, 383,145 European ancestry controls NA Affymetrix, Illumina [508495] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90080931 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.6: Ulcer of anus and rectum (Gene-based burden) 528 European ancestry cases, 387,402 European ancestry controls NA Illumina [185344] 0 anus disease http://www.ebi.ac.uk/efo/EFO_0009660 GCST90084252 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80: Cholelithiasis 17,665 European ancestry cases, 367,776 European ancestry controls 7,076 European ancestry cases, 108,108 European ancestry controls Affymetrix, Illumina [508493] 0 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90080297 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.8: Other specified diseases of anus and rectum (Gene-based burden) 3,323 European ancestry cases, 384,403 European ancestry controls NA Illumina [185343] 0 anus disease http://www.ebi.ac.uk/efo/EFO_0009660 GCST90084253 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.0: Panic disorder [episodic paroxysmal anxiety] 1,685 European ancestry cases, 383,717 European ancestry controls NA Affymetrix, Illumina [508463] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90079808 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63: Other diseases of intestine (Gene-based burden) 19,547 European ancestry cases, 366,223 European ancestry controls NA Illumina [185302] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084260 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.3: Type 2 diabetes mellitus with ophthalmic complications 4,180 European ancestry cases, 381,289 European ancestry controls NA Affymetrix, Illumina [508461] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079739 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.1: Perforation of intestine (nontraumatic) (Gene-based burden) 528 European ancestry cases, 387,395 European ancestry controls NA Illumina [185344] 0 intestinal perforation http://www.ebi.ac.uk/efo/EFO_1000987 GCST90084255 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.15: Urgency of urination 588 European ancestry cases, 384,738 European ancestry controls NA Affymetrix, Illumina [508441] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90080848 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.3: Ulcer of intestine (Gene-based burden) 930 European ancestry cases, 386,975 European ancestry controls NA Illumina [185344] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084256 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.10: Alcohol abuse, uncomplicated 624 European ancestry cases, 384,617 European ancestry controls NA Affymetrix, Illumina [508438] 0 alcohol abuse http://purl.obolibrary.org/obo/MONDO_0002046 GCST90079788 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.5: Polyp of colon (Gene-based burden) 15,366 European ancestry cases, 372,559 European ancestry controls NA Illumina [185344] 0 polyp of colon http://purl.obolibrary.org/obo/MONDO_0021400 GCST90084257 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z74: Problems related to care provider dependency 1,224 European ancestry cases, 384,269 European ancestry controls NA Affymetrix, Illumina [508425] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081319 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.8: Other specified diseases of intestine (Gene-based burden) 2,030 European ancestry cases, 385,889 European ancestry controls NA Illumina [185344] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084258 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02: Fracture of skull and facial bones 2,601 European ancestry cases, 382,658 European ancestry controls NA Affymetrix, Illumina [508420] 0 Skull Fractures http://www.ebi.ac.uk/efo/EFO_1001425 GCST90080949 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.9: Disease of intestine, unspecified (Gene-based burden) 1,019 European ancestry cases, 386,507 European ancestry controls NA Illumina [185325] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90084259 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16: Osteoarthritis of hip 15,772 European ancestry cases, 369,426 European ancestry controls NA Affymetrix, Illumina [508408] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90080412 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64: Hemorrhoids and perianal venous thrombosis (Gene-based burden) 10,256 European ancestry cases, 359,834 European ancestry controls NA Illumina [185058] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084263 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L65: Other nonscarring hair loss 834 European ancestry cases, 384,476 European ancestry controls NA Affymetrix, Illumina [508405] 0 alopecia http://purl.obolibrary.org/obo/MONDO_0004907 GCST90080358 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64.0: First degree hemorrhoids (Gene-based burden) 577 European ancestry cases, 387,353 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084261 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R60.0: Localized edema 2,631 European ancestry cases, 382,554 European ancestry controls NA Affymetrix, Illumina [508384] 0 edema http://www.ebi.ac.uk/efo/EFO_0009373 GCST90080888 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64.9: Unspecified hemorrhoids (Gene-based burden) 1,717 European ancestry cases, 386,213 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084262 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E03.9: Hypothyroidism, unspecified 19,694 European ancestry cases, 365,664 European ancestry controls 24,442 European ancestry cases, 90,108 European ancestry controls Affymetrix, Illumina [508382] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90079721 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K65: Peritonitis (Gene-based burden) 1,102 European ancestry cases, 386,626 European ancestry controls NA Illumina [185342] 0 peritonitis http://www.ebi.ac.uk/efo/EFO_0008588 GCST90084265 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H66.9: Otitis media, unspecified 1,110 European ancestry cases, 384,127 European ancestry controls NA Affymetrix, Illumina [508368] 0 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST90079934 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61: Open wound of wrist, hand and fingers 4,118 European ancestry cases, 381,007 European ancestry controls NA Affymetrix, Illumina [508279] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080997 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.9: Liver disease, unspecified (Gene-based burden) 928 European ancestry cases, 386,964 European ancestry controls NA Illumina [185343] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90084277 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R13: Aphagia and dysphagia 9,014 European ancestry cases, 376,259 European ancestry controls NA Affymetrix, Illumina [508272] 0 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST90080800 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80: Cholelithiasis (Gene-based burden) 17,665 European ancestry cases, 367,776 European ancestry controls NA Illumina [185298] 0 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90084283 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.3: Pain localized to other parts of lower abdomen 9,616 European ancestry cases, 375,446 European ancestry controls NA Affymetrix, Illumina [508216] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90080788 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.0: Calculus of gallbladder with acute cholecystitis (Gene-based burden) 1,911 European ancestry cases, 386,019 European ancestry controls NA Illumina [185344] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90084279 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41.3: Other amnesia 1,813 European ancestry cases, 383,312 European ancestry controls NA Affymetrix, Illumina [508216] 0 amnesia http://www.ebi.ac.uk/efo/EFO_1001454 GCST90080855 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.1: Calculus of gallbladder with other cholecystitis (Gene-based burden) 6,359 European ancestry cases, 381,571 European ancestry controls NA Illumina [185344] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90084280 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.1: Pain localized to upper abdomen 11,534 European ancestry cases, 373,596 European ancestry controls NA Affymetrix, Illumina [508213] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90080785 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.2: Calculus of gallbladder without cholecystitis (Gene-based burden) 10,288 European ancestry cases, 377,616 European ancestry controls NA Illumina [185344] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90084281 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R04.0: Epistaxis 3,559 European ancestry cases, 381,522 European ancestry controls 2,650 European ancestry cases, 75,486 European ancestry controls Affymetrix, Illumina [508209] 0 epistaxis http://www.ebi.ac.uk/efo/EFO_0003895 GCST90080761 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95.1: Menopausal and female climacteric states (Gene-based burden) 772 European ancestry cases, 209,359 European ancestry controls NA Illumina [179822] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084682 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Diabetes (UKB data field 20111) 30,682 European ancestry cases, 341,050 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078295 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95.2: Postmenopausal atrophic vaginitis (Gene-based burden) 1,317 European ancestry cases, 227,817 European ancestry controls NA Illumina [180826] 0 postmenopausal atrophic vaginitis http://purl.obolibrary.org/obo/MONDO_0001410 GCST90084683 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Heart disease (UKB data field 20111) 37,595 European ancestry cases, 334,137 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078288 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N97: Female infertility (Gene-based burden) 1,483 European ancestry cases, 207,556 European ancestry controls NA Illumina [179748] 0 female infertility http://www.ebi.ac.uk/efo/EFO_0008560 GCST90084686 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - High blood pressure (UKB data field 20111) 75,991 European ancestry cases, 295,741 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078294 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N97.9: Female infertility, unspecified (Gene-based burden) 1,163 European ancestry cases, 209,395 European ancestry controls NA Illumina [179846] 0 female infertility http://www.ebi.ac.uk/efo/EFO_0008560 GCST90084685 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Lung cancer (UKB data field 20111) 8,284 European ancestry cases, 363,448 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078290 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N99: Intraoperative and postprocedural complications and disorders of genitourinary system, not elsewhere classified (Gene-based burden) 1,366 European ancestry cases, 386,465 European ancestry controls NA Illumina [185343] 0 disease of genitourinary system http://www.ebi.ac.uk/efo/EFO_0009663 GCST90084688 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Stroke (UKB data field 20111) 12,254 European ancestry cases, 359,478 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078289 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N99.3: Prolapse of vaginal vault after hysterectomy (Gene-based burden) 565 European ancestry cases, 228,569 European ancestry controls NA Illumina [180826] 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90084687 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Alzheimers disease dementia (UKB data field 20111) 2,512 European ancestry cases, 369,220 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history of Alzheimer’s disease http://www.ebi.ac.uk/efo/EFO_0009268 GCST90078284 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O02: Other abnormal products of conception (Gene-based burden) 1,470 European ancestry cases, 209,448 European ancestry controls NA Illumina [179873] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084690 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Parkinsons disease (UKB data field 20111) 2,119 European ancestry cases, 369,613 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078285 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37: Candidiasis 8,778 European ancestry cases, 363,381 European ancestry controls NA Affymetrix, Illumina [496742] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90079560 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O42: Premature rupture of membranes (Gene-based burden) 1,136 European ancestry cases, 210,861 European ancestry controls NA Illumina [179940] 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90084704 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F32: Major depressive disorder, single episode 25,879 European ancestry cases, 346,278 European ancestry controls NA Affymetrix, Illumina [496720] 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90079804 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O42.9: Premature rupture of membranes, unspecified as to length of time between rupture and onset of labor (Gene-based burden) 566 European ancestry cases, 211,437 European ancestry controls NA Illumina [179915] 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90084703 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J30: Vasomotor and allergic rhinitis 7,482 European ancestry cases, 364,690 European ancestry controls NA Affymetrix, Illumina [496718] 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90080104 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O46: Antepartum hemorrhage, not elsewhere classified (Gene-based burden) 680 European ancestry cases, 211,264 European ancestry controls NA Illumina [179941] 0 Antepartum hemorrhage http://purl.obolibrary.org/obo/HP_0025328 GCST90084706 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Education score England (UKB data field 26414) 369,491 European ancestry individuals NA Affymetrix, Illumina [496701] 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90078953 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O46.9: Antepartum hemorrhage, unspecified (Gene-based burden) 639 European ancestry cases, 211,333 European ancestry controls NA Illumina [179941] 0 Antepartum hemorrhage http://purl.obolibrary.org/obo/HP_0025328 GCST90084705 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Index of Multiple Deprivation England (UKB data field 26410) 369,491 European ancestry individuals NA Affymetrix, Illumina [496701] 0 Townsend deprivation index http://www.ebi.ac.uk/efo/EFO_0009711 GCST90078952 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O47: False labor (Gene-based burden) 1,135 European ancestry cases, 210,857 European ancestry controls NA Illumina [179934] 0 Braxton-Hicks contractions http://www.ebi.ac.uk/efo/EFO_0009639 GCST90084708 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.5: Calculus of bile duct without cholangitis or cholecystitis (Gene-based burden) 2,940 European ancestry cases, 384,990 European ancestry controls NA Illumina [185344] 0 acalculous cholecystitis http://www.ebi.ac.uk/efo/EFO_1000790 GCST90084282 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83.5: Family history of eye and ear disorders 1,666 European ancestry cases, 383,607 European ancestry controls NA Affymetrix, Illumina [508206] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081341 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81: Cholecystitis (Gene-based burden) 3,403 European ancestry cases, 383,083 European ancestry controls NA Illumina [185323] 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90084287 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T46: Poisoning by, adverse effect of and underdosing of agents primarily affecting the cardiovascular system 621 European ancestry cases, 384,441 European ancestry controls NA Affymetrix, Illumina [508192] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081057 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81.0: Acute cholecystitis (Gene-based burden) 1,074 European ancestry cases, 386,294 European ancestry controls NA Illumina [185333] 0 Cholecystitis, Acute http://www.ebi.ac.uk/efo/EFO_1001289 GCST90084284 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S05: Injury of eye and orbit 662 European ancestry cases, 384,363 European ancestry controls NA Affymetrix, Illumina [508178] 0 eye injury http://www.ebi.ac.uk/efo/EFO_0009485 GCST90080950 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81.1: Chronic cholecystitis (Gene-based burden) 1,530 European ancestry cases, 386,400 European ancestry controls NA Illumina [185344] 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90084285 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L84: Corns and callosities 706 European ancestry cases, 384,517 European ancestry controls NA Affymetrix, Illumina [508155] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080370 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81.9: Cholecystitis, unspecified (Gene-based burden) 940 European ancestry cases, 386,668 European ancestry controls NA Illumina [185344] 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90084286 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.8: Other abnormalities of breathing 2,031 European ancestry cases, 383,067 European ancestry controls NA Affymetrix, Illumina [508147] 0 Abnormal pattern of respiration http://purl.obolibrary.org/obo/HP_0002793 GCST90080771 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K82: Other diseases of gallbladder (Gene-based burden) 2,278 European ancestry cases, 385,325 European ancestry controls NA Illumina [185339] 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90084290 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J45.909.: Unspecified asthma, uncomplicated 16,035 European ancestry cases, 369,001 European ancestry controls NA Affymetrix, Illumina [508146] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90080136 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K82.4: Cholesterolosis of gallbladder (Gene-based burden) 558 European ancestry cases, 387,372 European ancestry controls NA Illumina [185344] 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90084288 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M62: Other disorders of muscle 1,503 European ancestry cases, 383,520 European ancestry controls NA Affymetrix, Illumina [508144] 0 muscular disease http://www.ebi.ac.uk/efo/EFO_0002970 GCST90080515 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K82.8: Other specified diseases of gallbladder (Gene-based burden) 1,358 European ancestry cases, 386,568 European ancestry controls NA Illumina [185344] 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90084289 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N89: Other noninflammatory disorders of vagina (Gene-based burden) 5,496 European ancestry cases, 197,997 European ancestry controls NA Illumina [179401] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084665 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I10: Essential (primary) hypertension 105,117 European ancestry cases, 269,090 European ancestry controls 65,295 European ancestry cases, 53,444 European ancestry controls Affymetrix, Illumina [498884] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90079962 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N89.8: Other specified noninflammatory disorders of vagina (Gene-based burden) 1,410 European ancestry cases, 209,913 European ancestry controls NA Illumina [179903] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084664 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Testosterone levels (UKB data field 30850) 373,826 European ancestry individuals 5,319 European ancestry individuals Affymetrix, Illumina [498762] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90079042 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N90: Other noninflammatory disorders of vulva and perineum (Gene-based burden) 3,237 European ancestry cases, 205,577 European ancestry controls NA Illumina [179733] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084668 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09: Other symptoms and signs involving the circulatory and respiratory system 5,437 European ancestry cases, 369,196 European ancestry controls NA Affymetrix, Illumina [498761] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90080784 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N90.7: Vulvar cyst (Gene-based burden) 572 European ancestry cases, 228,562 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084666 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L29: Pruritus 5,379 European ancestry cases, 369,164 European ancestry controls NA Affymetrix, Illumina [498752] 0 Pruritus http://purl.obolibrary.org/obo/HP_0000989 GCST90080344 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N90.8: Other specified noninflammatory disorders of vulva and perineum (Gene-based burden) 706 European ancestry cases, 211,293 European ancestry controls NA Illumina [179941] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084667 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses or contact lenses use (age of onset) (UKB data field 2217) 374,837 European ancestry individuals NA Affymetrix, Illumina [498635] 1 age at onset, eye measurement http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0004731 GCST90078869 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N91: Absent, scanty and rare menstruation (Gene-based burden) 743 European ancestry cases, 208,695 European ancestry controls NA Illumina [179799] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084669 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.99: Other abnormal findings in urine 7,200 European ancestry cases, 366,949 European ancestry controls NA Affymetrix, Illumina [498527] 0 Abnormality of urine homeostasis http://purl.obolibrary.org/obo/HP_0003110 GCST90080916 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92: Excessive, frequent and irregular menstruation (Gene-based burden) 19,747 European ancestry cases, 181,191 European ancestry controls NA Illumina [179221] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90084674 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.615.: Unsatisfactory cytologic smear of cervix 5,620 European ancestry cases, 368,302 European ancestry controls NA Affymetrix, Illumina [498477] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080919 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.0: Excessive and frequent menstruation with regular cycle (Gene-based burden) 9,262 European ancestry cases, 202,718 European ancestry controls NA Illumina [179941] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90084670 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93: Other disorders of ear, not elsewhere classified 4,651 European ancestry cases, 369,518 European ancestry controls NA Affymetrix, Illumina [498469] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90079957 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.1: Excessive and frequent menstruation with irregular cycle (Gene-based burden) 2,965 European ancestry cases, 208,899 European ancestry controls NA Illumina [179930] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90084671 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03: Cellulitis and acute lymphangitis 12,973 European ancestry cases, 361,040 European ancestry controls NA Affymetrix, Illumina [498425] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90080331 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.3: Ovulation bleeding (Gene-based burden) 997 European ancestry cases, 228,137 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084672 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.9: Other and unspecified abnormal findings in urine 7,472 European ancestry cases, 366,444 European ancestry controls NA Affymetrix, Illumina [498326] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080917 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N92.6: Irregular menstruation, unspecified (Gene-based burden) 2,204 European ancestry cases, 208,273 European ancestry controls NA Illumina [179839] 0 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90084673 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J01: Acute sinusitis 7,767 European ancestry cases, 366,131 European ancestry controls NA Affymetrix, Illumina [498272] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90080085 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N93: Other abnormal uterine and vaginal bleeding (Gene-based burden) 5,757 European ancestry cases, 201,193 European ancestry controls NA Illumina [179623] 0 Metrorrhagia http://purl.obolibrary.org/obo/HP_0100608 GCST90084677 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12: Encounter for screening for malignant neoplasms 63,956 European ancestry cases, 309,749 European ancestry controls NA Affymetrix, Illumina [498169] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081211 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N93.0: Postcoital and contact bleeding (Gene-based burden) 1,256 European ancestry cases, 210,631 European ancestry controls NA Illumina [179929] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90084675 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of walks (UKB data field 874) 372,854 European ancestry individuals NA Affymetrix, Illumina [498092] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90079503 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N93.8: Other specified abnormal uterine and vaginal bleeding (Gene-based burden) 1,858 European ancestry cases, 209,539 European ancestry controls NA Illumina [179890] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084676 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z56: Problems related to employment and unemployment 7,388 European ancestry cases, 365,832 European ancestry controls NA Affymetrix, Illumina [497816] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081296 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94.1: Dyspareunia (Gene-based burden) 1,397 European ancestry cases, 209,321 European ancestry controls NA Illumina [179885] 0 Dyspareunia http://purl.obolibrary.org/obo/HP_0030016 GCST90084678 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06: Abnormalities of breathing 20,491 European ancestry cases, 352,838 European ancestry controls NA Affymetrix, Illumina [497782] 0 irregular respiration http://www.ebi.ac.uk/efo/EFO_0009841 GCST90080772 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94.6: Dysmenorrhea, unspecified (Gene-based burden) 1,843 European ancestry cases, 208,612 European ancestry controls NA Illumina [179852] 0 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90084679 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28: Immunization not carried out and underimmunization status 6,544 European ancestry cases, 366,674 European ancestry controls NA Affymetrix, Illumina [497670] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081228 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N94.8: Other specified conditions associated with female genital organs and menstrual cycle (Gene-based burden) 1,042 European ancestry cases, 209,765 European ancestry controls NA Illumina [179869] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084680 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Bowel cancer (UKB data field 20111) 9,037 European ancestry cases, 362,695 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078291 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95: Menopausal and other perimenopausal disorders (Gene-based burden) 19,021 European ancestry cases, 178,957 European ancestry controls NA Illumina [179007] 0 menopause http://www.ebi.ac.uk/efo/EFO_0003922 GCST90084684 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Breast cancer (UKB data field 20111) 16,443 European ancestry cases, 355,289 European ancestry controls 3,449 European ancestry cases, 120,979 European ancestry controls Affymetrix, Illumina [497474] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90078292 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N95.0: Postmenopausal bleeding (Gene-based burden) 10,065 European ancestry cases, 219,069 European ancestry controls NA Illumina [180826] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90084681 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Illnesses of siblings - Chronic bronchitis emphysema (UKB data field 20111) 10,430 European ancestry cases, 361,302 European ancestry controls NA Affymetrix, Illumina [497474] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90078293 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L81: Other disorders of pigmentation 1,269 European ancestry cases, 384,250 European ancestry controls NA Affymetrix, Illumina [508528] 0 pigmentation disease http://www.ebi.ac.uk/efo/EFO_1000755 GCST90080368 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K61.0: Anal abscess (Gene-based burden) 1,292 European ancestry cases, 386,634 European ancestry controls NA Illumina [185344] 0 Rectal abscess http://purl.obolibrary.org/obo/HP_0005224 GCST90084246 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.8: Abnormal findings on cytological and histological examination of urine 2,479 European ancestry cases, 382,756 European ancestry controls NA Affymetrix, Illumina [508512] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080914 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62: Other diseases of anus and rectum (Gene-based burden) 30,248 European ancestry cases, 347,295 European ancestry controls NA Illumina [185197] 0 anus disease, rectal disease http://www.ebi.ac.uk/efo/EFO_0009660, http://www.ebi.ac.uk/efo/EFO_0009685 GCST90084254 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S83.2: Tear of meniscus, current injury 813 European ancestry cases, 384,622 European ancestry controls NA Affymetrix, Illumina [508506] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081030 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.0: Anal polyp (Gene-based burden) 1,480 European ancestry cases, 386,450 European ancestry controls NA Illumina [185344] 0 anal polyp http://purl.obolibrary.org/obo/MONDO_0060766 GCST90084248 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.4: Infection following a procedure 5,665 European ancestry cases, 379,815 European ancestry controls NA Affymetrix, Illumina [508502] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081072 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.1: Rectal polyp (Gene-based burden) 8,321 European ancestry cases, 379,602 European ancestry controls NA Illumina [185344] 0 polyp of rectum http://purl.obolibrary.org/obo/MONDO_0021398 GCST90084249 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99: Dependence on enabling machines and devices, not elsewhere classified 3,699 European ancestry cases, 381,774 European ancestry controls 2,324 European ancestry cases, 34,705 European ancestry controls Affymetrix, Illumina [508502] 0 dependence on enabling machines and devices http://www.ebi.ac.uk/efo/EFO_0020981 GCST90081445 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.3: Rectal prolapse (Gene-based burden) 1,292 European ancestry cases, 386,638 European ancestry controls NA Illumina [185344] 0 Rectal prolapse http://purl.obolibrary.org/obo/HP_0002035 GCST90084250 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R59.1: Generalized enlarged lymph nodes 998 European ancestry cases, 384,487 European ancestry controls NA Affymetrix, Illumina [508495] 0 Lymphadenopathy http://purl.obolibrary.org/obo/HP_0002716 GCST90080886 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.5: Hemorrhage of anus and rectum (Gene-based burden) 15,430 European ancestry cases, 369,154 European ancestry controls NA Illumina [185283] 0 Gastrointestinal hemorrhage http://purl.obolibrary.org/obo/HP_0002239 GCST90084251 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X65: Intentional self-poisoning by and exposure to alcohol (Gene-based burden) 896 European ancestry cases, 387,034 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085132 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10: alcohol dependency 611 European ancestry cases, 328,441 European ancestry controls NA Affymetrix, Illumina [456274] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90077829 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y04: Assault by bodily force (Gene-based burden) 809 European ancestry cases, 386,995 European ancestry controls NA Illumina [185334] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085133 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R5382: chronic fatigue syndrome 1,753 European ancestry cases, 327,298 European ancestry controls NA Affymetrix, Illumina [456274] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90077896 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y93.9: Activity, unspecified 22,561 European ancestry cases, 335,235 European ancestry controls NA Affymetrix, Illumina [483966] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081175 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.8: Other specified symptoms and signs involving the circulatory and respiratory systems (Gene-based burden) 3,641 European ancestry cases, 373,833 European ancestry controls NA Illumina [185180] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90084769 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y93: Activity codes 22,575 European ancestry cases, 335,156 European ancestry controls NA Affymetrix, Illumina [483918] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081176 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R09.89: Other specified symptoms and signs involving the circulatory and respiratory systems (Gene-based burden) 2,494 European ancestry cases, 377,527 European ancestry controls NA Illumina [185238] 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90084768 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72: Problems related to lifestyle 41,581 European ancestry cases, 316,106 European ancestry controls NA Affymetrix, Illumina [483243] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081315 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10: Abdominal and pelvic pain (Gene-based burden) 42,433 European ancestry cases, 327,961 European ancestry controls NA Illumina [185001] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90084778 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractures 27,850 European ancestry cases, 328,502 European ancestry controls NA Affymetrix, Illumina [482745] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90081484 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.1: Pain localized to upper abdomen (Gene-based burden) 11,534 European ancestry cases, 373,596 European ancestry controls NA Illumina [185293] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90084771 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD SR: Ankylosing spondylitis - B27 negative 761 European ancestry cases, 355,581 European ancestry controls NA Affymetrix, Illumina [482262] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90079533 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.2: Pelvic and perineal pain (Gene-based burden) 3,323 European ancestry cases, 378,082 European ancestry controls NA Illumina [185227] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90084772 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergic disease 73,382 European ancestry cases, 280,642 European ancestry controls NA Affymetrix, Illumina [480928] 1 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081451 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.3: Pain localized to other parts of lower abdomen (Gene-based burden) 9,616 European ancestry cases, 375,446 European ancestry controls NA Illumina [185284] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90084774 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79: Other and unspecified soft tissue disorders, not elsewhere classified 40,514 European ancestry cases, 312,278 European ancestry controls NA Affymetrix, Illumina [479229] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080554 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.30: Lower abdominal pain, unspecified (Gene-based burden) 919 European ancestry cases, 384,254 European ancestry controls NA Illumina [185292] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90084773 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J06: Acute upper respiratory infections of multiple and unspecified sites 17,526 European ancestry cases, 335,507 European ancestry controls NA Affymetrix, Illumina [479061] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080092 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.4: Other and unspecified abdominal pain (Gene-based burden) 20,448 European ancestry cases, 367,482 European ancestry controls NA Illumina [185344] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90084775 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Direct bilirubin levels (UKB data field 30660) 351,671 European ancestry individuals 108,358 European ancestry individuals Affymetrix, Illumina [478148] 6 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90079021 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.8: Other abdominal pain (Gene-based burden) 604 European ancestry cases, 384,099 European ancestry controls NA Illumina [185276] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90084776 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes New Strict 11,970 European ancestry cases, 340,301 European ancestry controls NA Affymetrix, Illumina [477589] 1 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90081517 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.9: Unspecified abdominal pain (Gene-based burden) 4,176 European ancestry cases, 373,650 European ancestry controls NA Illumina [185157] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90084777 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - Above moderate/vigorous recommendation (UKB data field 22035) 190,022 European ancestry cases, 159,371 European ancestry controls NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078855 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I64: stroke 5,459 European ancestry cases, 323,593 European ancestry controls NA Affymetrix, Illumina [456275] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90077664 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X50: Overexertion and strenuous or repetitive movements (Gene-based burden) 1,283 European ancestry cases, 386,647 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085121 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E07: thyroid problem (not cancer) 1,135 European ancestry cases, 327,917 European ancestry controls NA Affymetrix, Illumina [456275] 0 thyroid disease http://www.ebi.ac.uk/efo/EFO_1000627 GCST90077727 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X50.9: Other and unspecified overexertion or strenuous movements or postures (Gene-based burden) 509 European ancestry cases, 387,421 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085120 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93: tinnitus tiniitis 1,297 European ancestry cases, 327,755 European ancestry controls NA Affymetrix, Illumina [456275] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90077954 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X59: Exposure to unspecified factor as an external cause of morbidity and mortality (Gene-based burden) 4,394 European ancestry cases, 383,536 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085123 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J03: tonsiltis 4,551 European ancestry cases, 324,501 European ancestry controls NA Affymetrix, Illumina [456275] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90077956 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X59.9: Exposure to unspecified factor - Unspecified place (Gene-based burden) 4,008 European ancestry cases, 383,922 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085122 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G45: transient ischaemic attack tia 1,611 European ancestry cases, 327,441 European ancestry controls NA Affymetrix, Illumina [456275] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90077666 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X60: Intentional self-poisoning by and exposure to nonopioid analgesics, antipyretics and antirheumatics (Gene-based burden) 1,572 European ancestry cases, 386,358 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085126 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55: trapped nerve compressed nerve 1,460 European ancestry cases, 327,592 European ancestry controls NA Affymetrix, Illumina [456275] 0 nerve compression syndrome http://www.ebi.ac.uk/efo/EFO_0009487 GCST90077738 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X60.0: Intentional self-poisoning by and exposure to nonopioid analgesics, antipyretics and antirheumatics - Home (Gene-based burden) 761 European ancestry cases, 387,169 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085124 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A15: tuberculosis tb 2,076 European ancestry cases, 326,976 European ancestry controls NA Affymetrix, Illumina [456275] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90077847 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X60.9: Intentional self-poisoning by and exposure to nonopioid analgesics, antipyretics and antirheumatics - Unspecified place (Gene-based burden) 930 European ancestry cases, 387,000 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085125 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11: type 2 diabetes 3,203 European ancestry cases, 325,849 European ancestry controls NA Affymetrix, Illumina [456275] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90077725 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X61: Intentional self-poisoning by and exposure to antiepileptic, sedative-hypnotic, antiparkinsonism and psychotropic drugs, not elsewhere classified (Gene-based burden) 1,591 European ancestry cases, 386,339 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085129 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K51: Ulcerative colitis 2,210 European ancestry cases, 326,842 European ancestry controls NA Affymetrix, Illumina [456275] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90077872 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X61.0: Intentional self-poisoning by and exposure to antiepileptic, sedative-hypnotic, antiparkinsonism and psychotropic drugs, not elsewhere classified - Home (Gene-based burden) 814 European ancestry cases, 387,116 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085127 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R15: urinary frequency incontinence 2,477 European ancestry cases, 326,575 European ancestry controls NA Affymetrix, Illumina [456275] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90077717 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X61.9: Intentional self-poisoning by and exposure to antiepileptic, sedative-hypnotic, antiparkinsonism and psychotropic drugs, not elsewhere classified - Unspecified place (Gene-based burden) 920 European ancestry cases, 387,010 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085128 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N390: Urinary tract infection or kidney infection 2,144 European ancestry cases, 326,908 European ancestry controls NA Affymetrix, Illumina [456275] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90077711 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X62: Intentional self-poisoning by and exposure to narcotics and psychodysleptics [hallucinogens], not elsewhere classified (Gene-based burden) 559 European ancestry cases, 387,371 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085130 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83: varicose veins 1,821 European ancestry cases, 327,231 European ancestry controls NA Affymetrix, Illumina [456275] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90077900 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X64: Intentional self-poisoning by and exposure to other and unspecified drugs, medicaments and biological substances (Gene-based burden) 659 European ancestry cases, 387,271 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085131 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A37: whooping cough pertussis 1,179 European ancestry cases, 327,873 European ancestry controls NA Affymetrix, Illumina [456275] 0 whooping cough http://www.ebi.ac.uk/efo/EFO_0000650 GCST90077950 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.3: Family history of stroke 7,178 European ancestry cases, 362,654 European ancestry controls NA Affymetrix, Illumina [494646] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081335 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O99.8: Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium (Gene-based burden) 803 European ancestry cases, 210,681 European ancestry controls NA Illumina [179907] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90084728 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64: Hemorrhoids and perianal venous thrombosis 10,256 European ancestry cases, 359,834 European ancestry controls NA Affymetrix, Illumina [494630] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080277 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 P29: Cardiovascular disorders originating in the perinatal period (Gene-based burden) 1,855 European ancestry cases, 384,135 European ancestry controls NA Illumina [185318] 0 cardiovascular disease, pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0009682 GCST90084732 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07.9: Chest pain, unspecified 9,797 European ancestry cases, 359,753 European ancestry controls NA Affymetrix, Illumina [494490] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90080778 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 P29.1: Neonatal cardiac dysrhythmia (Gene-based burden) 1,784 European ancestry cases, 384,880 European ancestry controls NA Illumina [185328] 0 perinatal disease http://www.ebi.ac.uk/efo/EFO_0010238 GCST90084731 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B35: Dermatophytosis 10,336 European ancestry cases, 359,321 European ancestry controls NA Affymetrix, Illumina [494327] 0 dermatophytosis http://purl.obolibrary.org/obo/MONDO_0004678 GCST90079553 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 P29.12: Neonatal bradycardia (Gene-based burden) 1,784 European ancestry cases, 384,880 European ancestry controls NA Illumina [185328] 0 perinatal disease http://www.ebi.ac.uk/efo/EFO_0010238 GCST90084730 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08: Other local infections of skin and subcutaneous tissue 6,404 European ancestry cases, 363,062 European ancestry controls NA Affymetrix, Illumina [494096] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080336 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Q21: Congenital malformations of cardiac septa (Gene-based burden) 724 European ancestry cases, 386,970 European ancestry controls NA Illumina [185340] 0 Abnormal cardiac septum morphology http://purl.obolibrary.org/obo/HP_0001671 GCST90084734 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19: Other and unspecified osteoarthritis 29,459 European ancestry cases, 339,413 European ancestry controls NA Affymetrix, Illumina [493896] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080427 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Q21.1: Atrial septal defect (Gene-based burden) 554 European ancestry cases, 387,345 European ancestry controls NA Illumina [185344] 0 atrial heart septal defect http://www.ebi.ac.uk/efo/EFO_1000825 GCST90084733 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53: Malaise and fatigue 11,044 European ancestry cases, 358,086 European ancestry controls NA Affymetrix, Illumina [493858] 0 malaise, Fatigue http://www.ebi.ac.uk/efo/EFO_0009641, http://purl.obolibrary.org/obo/HP_0012378 GCST90080878 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Q61: Cystic kidney disease (Gene-based burden) 578 European ancestry cases, 387,104 European ancestry controls NA Illumina [185332] 0 Cystic Kidney Disease http://www.ebi.ac.uk/efo/EFO_0008615 GCST90084735 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.89: Other problems related to lifestyle 11,281 European ancestry cases, 358,061 European ancestry controls NA Affymetrix, Illumina [493822] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081313 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00: Abnormalities of heart beat (Gene-based burden) 30,622 European ancestry cases, 334,318 European ancestry controls NA Illumina [184972] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90084740 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H10: Conjunctivitis 6,700 European ancestry cases, 362,087 European ancestry controls NA Affymetrix, Illumina [493802] 0 conjunctivitis http://www.ebi.ac.uk/efo/EFO_0009450 GCST90079880 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.0: Tachycardia, unspecified (Gene-based burden) 3,250 European ancestry cases, 383,673 European ancestry controls NA Illumina [185319] 0 Tachycardia http://purl.obolibrary.org/obo/HP_0001649 GCST90084736 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z72.8: Other problems related to lifestyle 11,329 European ancestry cases, 357,964 European ancestry controls NA Affymetrix, Illumina [493780] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081314 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.1: Bradycardia, unspecified (Gene-based burden) 19,591 European ancestry cases, 352,604 European ancestry controls NA Illumina [185103] 0 Bradycardia http://purl.obolibrary.org/obo/HP_0001662 GCST90084737 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T14: Injury of unspecified body region 4,277 European ancestry cases, 364,018 European ancestry controls NA Affymetrix, Illumina [493474] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081047 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.2: Palpitations (Gene-based burden) 9,306 European ancestry cases, 369,733 European ancestry controls NA Illumina [185191] 0 Palpitations http://purl.obolibrary.org/obo/HP_0001962 GCST90084738 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M77: Other enthesopathies 9,756 European ancestry cases, 358,940 European ancestry controls NA Affymetrix, Illumina [493466] 0 enthesopathy http://www.ebi.ac.uk/efo/EFO_0009666 GCST90080541 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.8: Other abnormalities of heart beat (Gene-based burden) 672 European ancestry cases, 385,774 European ancestry controls NA Illumina [185340] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90084739 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.5: Pain in joint 19,559 European ancestry cases, 348,462 European ancestry controls NA Affymetrix, Illumina [492966] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90080460 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R01: Cardiac murmurs and other cardiac sounds (Gene-based burden) 1,620 European ancestry cases, 384,413 European ancestry controls NA Illumina [185321] 0 Heart murmur http://purl.obolibrary.org/obo/HP_0030148 GCST90084742 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L30: Other and unspecified dermatitis 11,384 European ancestry cases, 355,935 European ancestry controls 25,551 European ancestry cases, 76,635 European ancestry controls Affymetrix, Illumina [492586] 0 dermatitis http://purl.obolibrary.org/obo/MONDO_0002406 GCST90080346 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R01.1: Cardiac murmur, unspecified (Gene-based burden) 1,507 European ancestry cases, 384,754 European ancestry controls NA Illumina [185323] 0 Heart murmur http://purl.obolibrary.org/obo/HP_0030148 GCST90084741 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19: Other symptoms and signs involving the digestive system and abdomen 26,789 European ancestry cases, 340,046 European ancestry controls NA Affymetrix, Illumina [492005] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080813 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R02: Gangrene, not elsewhere classified (Gene-based burden) 821 European ancestry cases, 387,109 European ancestry controls NA Illumina [185344] 0 gangrene http://www.ebi.ac.uk/efo/EFO_0008574 GCST90084743 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E66.9: Obesity, unspecified 170,856 European ancestry cases, 195,879 European ancestry controls NA Affymetrix, Illumina [492001] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90079763 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R03: Abnormal blood-pressure reading, without diagnosis (Gene-based burden) 7,318 European ancestry cases, 372,605 European ancestry controls NA Illumina [185240] 0 Abnormal systemic blood pressure http://purl.obolibrary.org/obo/HP_0030972 GCST90084746 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E66: Overweight and obesity 171,670 European ancestry cases, 194,798 European ancestry controls NA Affymetrix, Illumina [491745] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90079764 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R03.0: Elevated blood-pressure reading, without diagnosis of hypertension (Gene-based burden) 5,889 European ancestry cases, 374,125 European ancestry controls NA Illumina [185241] 0 Abnormal systemic blood pressure http://purl.obolibrary.org/obo/HP_0030972 GCST90084744 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R07: Pain in throat and chest 44,606 European ancestry cases, 321,826 European ancestry controls NA Affymetrix, Illumina [491693] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90080779 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R03.1: Nonspecific low blood-pressure reading (Gene-based burden) 1,483 European ancestry cases, 386,299 European ancestry controls NA Illumina [185343] 0 Abnormal systemic blood pressure http://purl.obolibrary.org/obo/HP_0030972 GCST90084745 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R87.61: Abnormal cytological findings in specimens from cervix uteri 11,386 European ancestry cases, 354,659 European ancestry controls NA Affymetrix, Illumina [491282] 0 Abnormal morphology of female internal genitalia http://purl.obolibrary.org/obo/HP_0000008 GCST90080921 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R04: Hemorrhage from respiratory passages (Gene-based burden) 6,031 European ancestry cases, 378,656 European ancestry controls NA Illumina [185298] 0 hemorrhage http://purl.obolibrary.org/obo/MP_0001914 GCST90084749 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.8: Other specified postprocedural states 11,319 European ancestry cases, 354,570 European ancestry controls NA Affymetrix, Illumina [491154] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081439 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R04.0: Epistaxis (Gene-based burden) 3,559 European ancestry cases, 381,522 European ancestry controls NA Illumina [185297] 0 epistaxis http://www.ebi.ac.uk/efo/EFO_0003895 GCST90084747 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.890.: Other specified postprocedural states 10,483 European ancestry cases, 355,405 European ancestry controls NA Affymetrix, Illumina [491138] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081437 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73: raynauds phenomenon disease 532 European ancestry cases, 328,520 European ancestry controls NA Affymetrix, Illumina [456275] 0 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90077938 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.0: Unspecified fall - Home (Gene-based burden) 2,010 European ancestry cases, 385,920 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085102 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12: rectal or colon adenoma polyps 1,492 European ancestry cases, 327,560 European ancestry controls NA Affymetrix, Illumina [456275] 0 adenomatous colon polyp http://www.ebi.ac.uk/efo/EFO_1000633 GCST90077868 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.2: Unspecified fall - School, other institution and public administrative area (Gene-based burden) 518 European ancestry cases, 387,412 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085103 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33: retinal detachment 1,460 European ancestry cases, 327,592 European ancestry controls NA Affymetrix, Illumina [456275] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90077760 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.4: Unspecified fall - Street and highway (Gene-based burden) 635 European ancestry cases, 387,295 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085104 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35: retinal problem 678 European ancestry cases, 328,374 European ancestry controls NA Affymetrix, Illumina [456275] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90077751 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.9: Unspecified fall - Unspecified place (Gene-based burden) 3,891 European ancestry cases, 384,039 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085105 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I00: rheumatic fever 1,208 European ancestry cases, 327,844 European ancestry controls NA Affymetrix, Illumina [456275] 0 rheumatic fever http://www.ebi.ac.uk/efo/EFO_1001160 GCST90077894 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.571.: Pain in right ankle and joints of right foot 988 European ancestry cases, 383,652 European ancestry controls NA Affymetrix, Illumina [507851] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90080458 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.3: Cellulitis and acute lymphangitis of trunk (Gene-based burden) 764 European ancestry cases, 387,073 European ancestry controls NA Illumina [185343] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90084315 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87: Other disorders of fluid, electrolyte and acid-base balance 9,393 European ancestry cases, 375,084 European ancestry controls NA Affymetrix, Illumina [507835] 0 Abnormality of metabolism/homeostasis http://purl.obolibrary.org/obo/HP_0001939 GCST90079779 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.9: Cellulitis and acute lymphangitis, unspecified (Gene-based burden) 742 European ancestry cases, 385,471 European ancestry controls NA Illumina [185328] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90084316 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R04: Hemorrhage from respiratory passages 6,031 European ancestry cases, 378,656 European ancestry controls NA Affymetrix, Illumina [507825] 0 hemorrhage http://purl.obolibrary.org/obo/MP_0001914 GCST90080763 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L05: Pilonidal cyst and sinus (Gene-based burden) 658 European ancestry cases, 386,608 European ancestry controls NA Illumina [185331] 0 Pilonidal sinus http://purl.obolibrary.org/obo/HP_0010769 GCST90084318 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57: Diverticular disease of intestine 37,004 European ancestry cases, 347,630 European ancestry controls NA Affymetrix, Illumina [507822] 0 diverticulitis http://www.ebi.ac.uk/efo/EFO_1001460 GCST90080249 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08: Other local infections of skin and subcutaneous tissue (Gene-based burden) 6,404 European ancestry cases, 363,062 European ancestry controls NA Illumina [185042] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084322 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.1: Bradycardia, unspecified 19,591 European ancestry cases, 352,604 European ancestry controls NA Affymetrix, Illumina [496670] 0 Bradycardia http://purl.obolibrary.org/obo/HP_0001662 GCST90080751 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O47.1: False labor at or after 37 completed weeks of gestation (Gene-based burden) 703 European ancestry cases, 228,431 European ancestry controls NA Illumina [180820] 0 Braxton-Hicks contractions http://www.ebi.ac.uk/efo/EFO_0009639 GCST90084707 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91: Other and unspecified hearing loss 8,261 European ancestry cases, 363,853 European ancestry controls NA Affymetrix, Illumina [496646] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90079951 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O48: Late pregnancy (Gene-based burden) 1,268 European ancestry cases, 210,715 European ancestry controls NA Illumina [179879] 0 post term pregnancy http://www.ebi.ac.uk/efo/EFO_0009681 GCST90084709 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.7: Diarrhea, unspecified 6,369 European ancestry cases, 365,632 European ancestry controls NA Affymetrix, Illumina [496625] 0 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST90080811 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O60: Preterm labor (Gene-based burden) 690 European ancestry cases, 211,192 European ancestry controls NA Illumina [179938] 0 premature birth http://www.ebi.ac.uk/efo/EFO_0003917 GCST90084710 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.9: Dorsalgia, unspecified 13,158 European ancestry cases, 358,552 European ancestry controls NA Affymetrix, Illumina [496470] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90080512 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O63: Long labor (Gene-based burden) 2,057 European ancestry cases, 209,943 European ancestry controls NA Illumina [179937] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90084712 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82: Other and unspecified abnormal findings in urine 9,916 European ancestry cases, 361,639 European ancestry controls NA Affymetrix, Illumina [496391] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080918 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O63.1: Prolonged second stage (of labor) (Gene-based burden) 1,487 European ancestry cases, 227,647 European ancestry controls NA Illumina [180823] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90084711 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J02.9: Acute pharyngitis, unspecified 6,744 European ancestry cases, 365,218 European ancestry controls NA Affymetrix, Illumina [496354] 0 acute pharyngitis http://www.ebi.ac.uk/efo/EFO_0009657 GCST90080086 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68: Labor and delivery complicated by abnormality of fetal acid-base balance (Gene-based burden) 3,526 European ancestry cases, 225,608 European ancestry controls NA Illumina [180826] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084717 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.8: Personal history of other specified conditions 50,319 European ancestry cases, 321,392 European ancestry controls NA Affymetrix, Illumina [496308] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081379 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.0: Labour and delivery complicated by fetal heart rate anomaly (Gene-based burden) 1,408 European ancestry cases, 227,726 European ancestry controls NA Illumina [180825] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084713 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41: Other anxiety disorders 17,585 European ancestry cases, 353,730 European ancestry controls NA Affymetrix, Illumina [496217] 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90079812 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.1: Labour and delivery complicated by meconium in amniotic fluid (Gene-based burden) 962 European ancestry cases, 228,172 European ancestry controls NA Illumina [180826] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084714 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z53.9: Procedure and treatment not carried out, unspecified reason 12,610 European ancestry cases, 358,984 European ancestry controls NA Affymetrix, Illumina [496175] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081291 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.2: Labour and delivery complicated by fetal heart rate anomaly with meconium in amniotic fluid (Gene-based burden) 504 European ancestry cases, 228,630 European ancestry controls NA Illumina [180825] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084715 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.8: Other malaise and fatigue 6,340 European ancestry cases, 365,215 European ancestry controls NA Affymetrix, Illumina [496130] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90080877 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O68.8: Labour and delivery complicated by other evidence of fetal stress (Gene-based burden) 539 European ancestry cases, 228,595 European ancestry controls NA Illumina [180826] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084716 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L82: Seborrheic keratosis 10,168 European ancestry cases, 361,048 European ancestry controls NA Affymetrix, Illumina [495971] 0 seborrheic keratosis http://www.ebi.ac.uk/efo/EFO_0005584 GCST90080369 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O69: Labor and delivery complicated by umbilical cord complications (Gene-based burden) 664 European ancestry cases, 211,335 European ancestry controls NA Illumina [179729] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084718 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R51: Headache 17,773 European ancestry cases, 353,610 European ancestry controls NA Affymetrix, Illumina [495949] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90080870 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O70: Perineal laceration during delivery (Gene-based burden) 5,700 European ancestry cases, 206,171 European ancestry controls NA Illumina [179932] 0 perineal laceration during delivery http://www.ebi.ac.uk/efo/EFO_0009816 GCST90084721 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R42: Dizziness and giddiness 14,711 European ancestry cases, 356,152 European ancestry controls NA Affymetrix, Illumina [495724] 0 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90080858 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O70.0: First degree perineal laceration during delivery (Gene-based burden) 2,364 European ancestry cases, 209,629 European ancestry controls NA Illumina [179937] 0 perineal laceration during delivery http://www.ebi.ac.uk/efo/EFO_0009816 GCST90084719 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H57: Other disorders of eye and adnexa 4,926 European ancestry cases, 365,834 European ancestry controls NA Affymetrix, Illumina [495517] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079926 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O70.1: Second degree perineal laceration during delivery (Gene-based burden) 3,499 European ancestry cases, 225,635 European ancestry controls NA Illumina [180825] 0 perineal laceration during delivery http://www.ebi.ac.uk/efo/EFO_0009816 GCST90084720 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F17: Nicotine dependence 32,828 European ancestry cases, 337,667 European ancestry controls 28,112 European ancestry cases, 87,083 European ancestry controls Affymetrix, Illumina [495261] 0 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90079798 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O72: Postpartum hemorrhage (Gene-based burden) 1,418 European ancestry cases, 210,220 European ancestry controls NA Illumina [179930] 0 postpartum hemorrhage http://www.ebi.ac.uk/efo/EFO_0009579 GCST90084723 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H61: Other disorders of external ear 14,555 European ancestry cases, 355,834 European ancestry controls NA Affymetrix, Illumina [495135] 0 external ear disease http://www.ebi.ac.uk/efo/EFO_0009668 GCST90079930 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O72.1: Other immediate postpartum hemorrhage (Gene-based burden) 1,046 European ancestry cases, 228,088 European ancestry controls NA Illumina [180825] 0 postpartum hemorrhage http://www.ebi.ac.uk/efo/EFO_0009579 GCST90084722 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10: Abdominal and pelvic pain 42,433 European ancestry cases, 327,961 European ancestry controls NA Affymetrix, Illumina [494994] 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90080792 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O75: Other complications of labor and delivery, not elsewhere classified (Gene-based burden) 848 European ancestry cases, 210,661 European ancestry controls NA Illumina [179913] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084724 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.8: Other specified personal risk factors, not elsewhere classified 5,202 European ancestry cases, 364,578 European ancestry controls NA Affymetrix, Illumina [494984] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90081402 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O80: Encounter for full-term uncomplicated delivery (Gene-based burden) 9,148 European ancestry cases, 196,653 European ancestry controls NA Illumina [179580] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90084726 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.89: Other specified personal risk factors, not elsewhere classified 5,122 European ancestry cases, 364,657 European ancestry controls NA Affymetrix, Illumina [494982] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90081401 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O80.0: Spontaneous vertex delivery (Gene-based burden) 1,665 European ancestry cases, 227,469 European ancestry controls NA Illumina [180825] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90084725 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63: Other problems related to primary support group, including family circumstances 4,579 European ancestry cases, 365,694 European ancestry controls NA Affymetrix, Illumina [494900] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081304 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O99: Other maternal diseases classifiable elsewhere but complicating pregnancy, childbirth and the puerperium (Gene-based burden) 2,035 European ancestry cases, 209,171 European ancestry controls NA Illumina [179893] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90084729 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39: Other disorders of urinary system 31,925 European ancestry cases, 337,879 European ancestry controls NA Affymetrix, Illumina [494647] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90080616 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 O99.0: Anemia complicating pregnancy, childbirth and the puerperium (Gene-based burden) 922 European ancestry cases, 228,212 European ancestry controls NA Illumina [180441] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90084727 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W22: Striking against or struck by other objects (Gene-based burden) 959 European ancestry cases, 386,954 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085107 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06: rheumatoid arthritis 4,752 European ancestry cases, 324,300 European ancestry controls NA Affymetrix, Illumina [456275] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90077874 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W23: Caught, crushed, jammed or pinched in or between objects (Gene-based burden) 975 European ancestry cases, 386,952 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085108 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L71: Rosacea 754 European ancestry cases, 328,298 European ancestry controls NA Affymetrix, Illumina [456275] 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90077986 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W25: Contact with sharp glass (Gene-based burden) 610 European ancestry cases, 387,268 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085109 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B06: rubella german measles 1,961 European ancestry cases, 327,091 European ancestry controls NA Affymetrix, Illumina [456275] 0 rubella http://www.ebi.ac.uk/efo/EFO_1002026 GCST90077946 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W26: Contact with other sharp objects (Gene-based burden) 568 European ancestry cases, 387,347 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085110 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D86: Sarcoidosis 746 European ancestry cases, 328,306 European ancestry controls NA Affymetrix, Illumina [456275] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90077805 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W29: Contact with other powered hand tools and household machinery (Gene-based burden) 552 European ancestry cases, 387,377 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085111 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A38: scarlet fever scarlatina 936 European ancestry cases, 328,116 European ancestry controls NA Affymetrix, Illumina [456275] 0 scarlet fever http://www.ebi.ac.uk/efo/EFO_0007477 GCST90077993 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W31: Contact with other and unspecified machinery (Gene-based burden) 564 European ancestry cases, 387,285 European ancestry controls NA Illumina [185342] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085112 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: sciatica 4,079 European ancestry cases, 324,973 European ancestry controls NA Affymetrix, Illumina [456275] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90077888 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W44: Foreign body entering into or through eye or natural orifice causing accidental injury (Gene-based burden) 690 European ancestry cases, 387,240 European ancestry controls NA Illumina [185344] 0 eye foreign body http://www.ebi.ac.uk/efo/EFO_1001322 GCST90085114 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B02: shingles 880 European ancestry cases, 328,172 European ancestry controls NA Affymetrix, Illumina [456275] 0 susceptibility to shingles measurement http://www.ebi.ac.uk/efo/EFO_0008401 GCST90077952 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W44.9: Foreign body entering into or through eye or natural orifice causing accidental injury - Unspecified place (Gene-based burden) 509 European ancestry cases, 387,421 European ancestry controls NA Illumina [185344] 0 eye foreign body http://www.ebi.ac.uk/efo/EFO_1001322 GCST90085113 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47: sleep apnoea 1,429 European ancestry cases, 327,623 European ancestry controls NA Affymetrix, Illumina [456275] 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90077682 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W45: Foreign body or object entering through skin (Gene-based burden) 648 European ancestry cases, 386,768 European ancestry controls NA Illumina [185340] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085115 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48: Spine arthritis or spondylitis 3,855 European ancestry cases, 325,197 European ancestry controls NA Affymetrix, Illumina [456275] 0 spondylitis http://purl.obolibrary.org/obo/MONDO_0003937 GCST90077782 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W54: Contact with dog (Gene-based burden) 892 European ancestry cases, 385,017 European ancestry controls NA Illumina [185305] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085116 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J93: spontaneous pneumothorax recurrent pneumothorax 839 European ancestry cases, 328,212 European ancestry controls NA Affymetrix, Illumina [456275] 0 Spontaneous pneumothorax http://purl.obolibrary.org/obo/HP_0002108 GCST90077686 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W55: Contact with other mammals (Gene-based burden) 553 European ancestry cases, 386,361 European ancestry controls NA Illumina [185324] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085117 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31: stomach disorder 924 European ancestry cases, 328,128 European ancestry controls NA Affymetrix, Illumina [456275] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90077688 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W57: Bitten or stung by nonvenomous insect and other nonvenomous arthropods (Gene-based burden) 549 European ancestry cases, 386,401 European ancestry controls NA Illumina [185330] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085118 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F43: stress 840 European ancestry cases, 328,212 European ancestry controls NA Affymetrix, Illumina [456275] 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90077960 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W64: Exposure to other animate mechanical forces (Gene-based burden) 748 European ancestry cases, 382,877 European ancestry controls NA Illumina [185274] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085119 Exome-wide sequencing 2021-05-06 33888908 Pirastu N 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888908 Genetic analyses identify widespread sex-differential participation bias. Biological sex 1,301,549 European ancestry cases, 1,160,583 European ancestry controls NA Illumina [13288253] (imputed) 158 biological sex http://purl.obolibrary.org/obo/PATO_0000047 GCST90013473 Genome-wide genotyping array 2021-05-06 33888908 Pirastu N 2021-04-22 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33888908 Genetic analyses identify widespread sex-differential participation bias. Biological sex (age adjusted) 245,351 European ancestry cases, 206,951 European ancestry controls NA Affymetrix [25647815] (imputed) 0 biological sex http://purl.obolibrary.org/obo/PATO_0000047 GCST90013474 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10.9: Alcohol use, unspecified 109,309 European ancestry cases, 235,868 European ancestry controls NA Affymetrix, Illumina [471725] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90079792 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R17: Unspecified jaundice (Gene-based burden) 1,179 European ancestry cases, 386,397 European ancestry controls NA Illumina [185341] 0 Jaundice http://purl.obolibrary.org/obo/HP_0000952 GCST90084792 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F10: Alcohol related disorders 114,302 European ancestry cases, 230,584 European ancestry controls NA Affymetrix, Illumina [471419] 0 alcohol-related disorders http://purl.obolibrary.org/obo/MONDO_0021698 GCST90079793 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R18: Ascites (Gene-based burden) 2,103 European ancestry cases, 385,762 European ancestry controls NA Illumina [185344] 0 Ascites http://purl.obolibrary.org/obo/HP_0001541 GCST90084793 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma-COPD overlap syndrome 14,114 European ancestry cases, 330,697 European ancestry controls NA Affymetrix, Illumina [471303] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081446 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19: Other symptoms and signs involving the digestive system and abdomen (Gene-based burden) 26,789 European ancestry cases, 340,046 European ancestry controls NA Illumina [184960] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90084799 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease - composite 14,114 European ancestry cases, 330,697 European ancestry controls NA Affymetrix, Illumina [471303] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90081468 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.0: Intra-abdominal and pelvic swelling, mass and lump (Gene-based burden) 1,552 European ancestry cases, 384,513 European ancestry controls NA Illumina [185311] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90084794 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. FEV1 FVC ratio Z score (UKB data field 20258) 343,302 European ancestry individuals 25,467 European ancestry individuals Affymetrix, Illumina [469352] 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90078390 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.4: Change in bowel habit (Gene-based burden) 15,857 European ancestry cases, 366,696 European ancestry controls NA Illumina [185276] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90084795 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 Z score (UKB data field 20256) 343,302 European ancestry individuals 25,470 European ancestry individuals Affymetrix, Illumina [469352] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90078388 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.5: Other fecal abnormalities (Gene-based burden) 2,737 European ancestry cases, 383,417 European ancestry controls NA Illumina [185329] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90084796 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced vital capacity FVC Z score (UKB data field 20257) 343,302 European ancestry individuals 25,470 European ancestry individuals Affymetrix, Illumina [469352] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90078389 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.7: Diarrhea, unspecified (Gene-based burden) 6,369 European ancestry cases, 365,632 European ancestry controls NA Illumina [185062] 0 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST90084797 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.9: Encounter for screening, unspecified 24,217 European ancestry cases, 317,766 European ancestry controls NA Affymetrix, Illumina [468923] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081219 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.8: Other specified symptoms and signs involving the digestive system and abdomen (Gene-based burden) 2,178 European ancestry cases, 384,747 European ancestry controls NA Illumina [185324] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90084798 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.4: Family history of ischemic heart disease and other diseases of the circulatory system 43,852 European ancestry cases, 296,393 European ancestry controls 8,696 European ancestry cases, 33,306 European ancestry controls Affymetrix, Illumina [467871] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081337 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20: Disturbances of skin sensation (Gene-based burden) 7,669 European ancestry cases, 367,888 European ancestry controls NA Illumina [185188] 0 disturbance of skin sensation http://www.ebi.ac.uk/efo/EFO_0009522 GCST90084803 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.49: Family history of ischemic heart disease and other diseases of the circulatory system 29,712 European ancestry cases, 309,459 European ancestry controls NA Affymetrix, Illumina [466915] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081336 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20.0: Anesthesia of skin (Gene-based burden) 887 European ancestry cases, 383,058 European ancestry controls NA Illumina [185292] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084800 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: Dorsalgia 50,434 European ancestry cases, 288,924 European ancestry controls NA Affymetrix, Illumina [466650] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90080513 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20.2: Paresthesia of skin (Gene-based burden) 3,860 European ancestry cases, 376,820 European ancestry controls NA Illumina [185241] 0 Paresthesia http://purl.obolibrary.org/obo/HP_0003401 GCST90084801 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82: Family history of certain disabilities and chronic diseases (leading to disablement) 48,407 European ancestry cases, 284,122 European ancestry controls NA Affymetrix, Illumina [460529] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081339 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R20.8: Other disturbances of skin sensation (Gene-based burden) 3,285 European ancestry cases, 382,547 European ancestry controls NA Illumina [185323] 0 disturbance of skin sensation http://www.ebi.ac.uk/efo/EFO_0009522 GCST90084802 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13: Encounter for screening for other diseases and disorders 40,310 European ancestry cases, 291,703 European ancestry controls NA Affymetrix, Illumina [459652] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081220 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R21: Rash and other nonspecific skin eruption (Gene-based burden) 13,788 European ancestry cases, 351,645 European ancestry controls NA Illumina [184989] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90084804 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hypertension nephropathy (no type 2 diabetes) 3,668 European ancestry cases, 328,410 European ancestry controls NA Affymetrix, Illumina [459131] 0 Nephropathy http://purl.obolibrary.org/obo/HP_0000112 GCST90081486 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22: Localized swelling, mass and lump of skin and subcutaneous tissue (Gene-based burden) 3,876 European ancestry cases, 374,735 European ancestry controls NA Illumina [185175] 0 primary lymphedema http://purl.obolibrary.org/obo/MONDO_0019175 GCST90084809 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy hypersensitivity anaphylaxis 3,277 European ancestry cases, 328,477 European ancestry controls NA Affymetrix, Illumina [458873] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90077806 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.0: Localized swelling, mass and lump, head (Gene-based burden) 528 European ancestry cases, 386,502 European ancestry controls NA Illumina [185335] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90084805 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy or anaphylactic reaction to drug 4,757 European ancestry cases, 326,997 European ancestry controls NA Affymetrix, Illumina [458873] 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90077813 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.1: Localized swelling, mass and lump, neck (Gene-based burden) 676 European ancestry cases, 386,074 European ancestry controls NA Illumina [185336] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90084806 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy or anaphylactic reaction to food 2,207 European ancestry cases, 329,547 European ancestry controls NA Affymetrix, Illumina [458873] 0 food allergy http://www.ebi.ac.uk/efo/EFO_1001890 GCST90077811 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.4: Localized swelling, mass and lump, lower limb (Gene-based burden) 681 European ancestry cases, 387,076 European ancestry controls NA Illumina [185341] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90084807 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Allergy to house dust mite 533 European ancestry cases, 331,221 European ancestry controls NA Affymetrix, Illumina [458873] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90077991 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.9: Localized swelling, mass and lump, unspecified (Gene-based burden) 1,032 European ancestry cases, 381,474 European ancestry controls NA Illumina [185235] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90084808 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anaemia 987 European ancestry cases, 330,767 European ancestry controls NA Affymetrix, Illumina [458873] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90077851 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R23: Other skin changes (Gene-based burden) 1,606 European ancestry cases, 381,328 European ancestry controls NA Illumina [185241] 0 Abnormality of the skin http://purl.obolibrary.org/obo/HP_0000951 GCST90084811 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Angina 14,285 European ancestry cases, 317,469 European ancestry controls NA Affymetrix, Illumina [458873] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90077655 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R23.8: Other skin changes (Gene-based burden) 598 European ancestry cases, 385,129 European ancestry controls NA Illumina [185307] 0 Abnormality of the skin http://purl.obolibrary.org/obo/HP_0000951 GCST90084810 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankylosing spondylitis 1,239 European ancestry cases, 330,515 European ancestry controls NA Affymetrix, Illumina [458873] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90077785 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R25: Abnormal involuntary movements (Gene-based burden) 2,585 European ancestry cases, 379,959 European ancestry controls NA Illumina [185227] 0 Abnormality of movement http://purl.obolibrary.org/obo/HP_0100022 GCST90084814 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anxiety or panic attacks 7,097 European ancestry cases, 324,657 European ancestry controls NA Affymetrix, Illumina [458873] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90077763 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R25.1: Tremor, unspecified (Gene-based burden) 1,055 European ancestry cases, 385,301 European ancestry controls NA Illumina [185310] 0 Tremor http://purl.obolibrary.org/obo/HP_0001337 GCST90084812 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Appendicitis 4,527 European ancestry cases, 327,227 European ancestry controls NA Affymetrix, Illumina [458873] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90077903 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R25.2: Cramp and spasm (Gene-based burden) 1,279 European ancestry cases, 382,797 European ancestry controls NA Illumina [185259] 0 muscle cramp http://www.ebi.ac.uk/efo/EFO_0009846 GCST90084813 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arthritis nos 4,982 European ancestry cases, 326,772 European ancestry controls NA Affymetrix, Illumina [458873] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90077927 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R26: Abnormalities of gait and mobility (Gene-based burden) 3,394 European ancestry cases, 382,985 European ancestry controls NA Illumina [185319] 0 Gait disturbance http://purl.obolibrary.org/obo/HP_0001288 GCST90084816 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma 50,973 European ancestry cases, 280,781 European ancestry controls NA Affymetrix, Illumina [458873] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90077671 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R26.8: Other abnormalities of gait and mobility (Gene-based burden) 2,708 European ancestry cases, 384,407 European ancestry controls NA Illumina [185334] 0 Gait disturbance http://purl.obolibrary.org/obo/HP_0001288 GCST90084815 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Atrial fibrillation 3,921 European ancestry cases, 327,833 European ancestry controls NA Affymetrix, Illumina [458873] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90077881 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R27: Other lack of coordination (Gene-based burden) 775 European ancestry cases, 385,556 European ancestry controls NA Illumina [185327] 0 Abnormality of movement http://purl.obolibrary.org/obo/HP_0100022 GCST90084817 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Back pain 3,955 European ancestry cases, 327,799 European ancestry controls NA Affymetrix, Illumina [458873] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90077923 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29: Other symptoms and signs involving the nervous and musculoskeletal systems (Gene-based burden) 6,035 European ancestry cases, 375,445 European ancestry controls NA Illumina [185253] 0 Abnormality of the nervous system, Abnormality of the musculature, Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000707, http://purl.obolibrary.org/obo/HP_0003011, http://purl.obolibrary.org/obo/HP_0000924 GCST90084822 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Back problem 7,766 European ancestry cases, 323,988 European ancestry controls NA Affymetrix, Illumina [458873] 0 Abnormality of the cervical spine http://purl.obolibrary.org/obo/HP_0003319 GCST90077771 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.6: Repeated falls (Gene-based burden) 3,229 European ancestry cases, 383,252 European ancestry controls NA Illumina [185315] 0 Abnormality of movement http://purl.obolibrary.org/obo/HP_0100022 GCST90084818 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Benign breast lump 1,671 European ancestry cases, 330,083 European ancestry controls NA Affymetrix, Illumina [458873] 0 breast benign neoplasm http://purl.obolibrary.org/obo/MONDO_0000620 GCST90077989 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.8: Other symptoms and signs involving the nervous and musculoskeletal systems (Gene-based burden) 2,856 European ancestry cases, 380,793 European ancestry controls NA Illumina [185304] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90084821 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bladder problem (not cancer) 2,768 European ancestry cases, 328,986 European ancestry controls NA Affymetrix, Illumina [458873] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90077714 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.89: Other symptoms and signs involving the musculoskeletal system (Gene-based burden) 585 European ancestry cases, 384,062 European ancestry controls NA Illumina [185315] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90084820 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blistering desquamating skin disorder 708 European ancestry cases, 331,046 European ancestry controls NA Affymetrix, Illumina [458873] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90077857 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.898.: Other symptoms and signs involving the musculoskeletal system (Gene-based burden) 585 European ancestry cases, 384,066 European ancestry controls NA Illumina [185315] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90084819 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bone disorder 988 European ancestry cases, 330,766 European ancestry controls 2,787 European ancestry cases, 116,004 European ancestry controls Affymetrix, Illumina [458873] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90077769 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R30: Pain associated with micturition (Gene-based burden) 3,783 European ancestry cases, 376,929 European ancestry controls NA Illumina [185225] 0 dysuria http://www.ebi.ac.uk/efo/EFO_0003901 GCST90084824 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Breast cysts 1,900 European ancestry cases, 329,854 European ancestry controls NA Affymetrix, Illumina [458873] 0 breast cyst http://www.ebi.ac.uk/efo/EFO_1000848 GCST90077802 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R30.0: Dysuria (Gene-based burden) 3,624 European ancestry cases, 377,076 European ancestry controls NA Illumina [185225] 0 dysuria http://www.ebi.ac.uk/efo/EFO_0003901 GCST90084823 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bronchiectasis 1,129 European ancestry cases, 330,625 European ancestry controls NA Affymetrix, Illumina [458873] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90077677 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31: Hematuria (Gene-based burden) 19,710 European ancestry cases, 363,299 European ancestry controls NA Illumina [185275] 0 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST90084828 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bronchitis 3,807 European ancestry cases, 327,947 European ancestry controls NA Affymetrix, Illumina [458873] 0 bronchial disease http://www.ebi.ac.uk/efo/EFO_1002018 GCST90077830 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31.2: Other microscopic hematuria (Gene-based burden) 541 European ancestry cases, 385,315 European ancestry controls NA Illumina [185321] 0 Microscopic hematuria http://purl.obolibrary.org/obo/HP_0002907 GCST90084826 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carpal tunnel syndrome 928 European ancestry cases, 330,826 European ancestry controls NA Affymetrix, Illumina [458873] 0 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90077929 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31.29: Other microscopic hematuria (Gene-based burden) 541 European ancestry cases, 385,315 European ancestry controls NA Illumina [185321] 0 Microscopic hematuria http://purl.obolibrary.org/obo/HP_0002907 GCST90084825 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract 8,629 European ancestry cases, 323,125 European ancestry controls 14,357 European ancestry cases, 100,935 European ancestry controls Affymetrix, Illumina [458873] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90077756 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31.9: Hematuria, unspecified (Gene-based burden) 2,270 European ancestry cases, 380,420 European ancestry controls NA Illumina [185259] 0 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST90084827 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cervical spondylosis 3,241 European ancestry cases, 328,513 European ancestry controls NA Affymetrix, Illumina [458873] 0 cervical spondylosis http://www.ebi.ac.uk/efo/EFO_0009610 GCST90077891 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-06-17 33242228 Niu Y 2020-11-26 J Cell Mol Med www.ncbi.nlm.nih.gov/pubmed/33242228 Genome-wide association study identifies 7q11.22 and 7q36.3 associated with noise-induced hearing loss among Chinese population. Hearing loss in noise exposure 89 Chinese ancestry cases, 209 Chinese ancestry controls 53 Chinese ancestry cases, 360 Chinese ancestry controls Illumina [3830431] (imputed) 2 noise-induced hearing loss http://www.ebi.ac.uk/efo/EFO_1001254 GCST011920 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.0: Nausea (Gene-based burden) 827 European ancestry cases, 383,789 European ancestry controls NA Illumina [185284] 0 Nausea http://purl.obolibrary.org/obo/HP_0002018 GCST90084779 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Physical activity group - high (UKB data field 22032) 141,453 European ancestry cases, 207,940 European ancestry controls NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078853 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.1: Vomiting (Gene-based burden) 656 European ancestry cases, 383,646 European ancestry controls NA Illumina [185266] 0 Vomiting http://purl.obolibrary.org/obo/HP_0002013 GCST90084782 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Physical activity group - low (UKB data field 22032) 65,285 European ancestry cases, 284,108 European ancestry controls NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078851 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.10: Vomiting, unspecified (Gene-based burden) 595 European ancestry cases, 384,080 European ancestry controls NA Illumina [185269] 0 Vomiting http://purl.obolibrary.org/obo/HP_0002013 GCST90084781 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Physical activity group - moderate (UKB data field 22032) 142,655 European ancestry cases, 206,738 European ancestry controls NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078852 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.103.11: Vomiting (Gene-based burden) 15,689 European ancestry cases, 366,456 European ancestry controls NA Illumina [185225] 0 Vomiting http://purl.obolibrary.org/obo/HP_0002013 GCST90084780 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - minutes per week for moderate activity (UKB data field 22038) 349,393 European ancestry individuals NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078858 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R12: Heartburn (Gene-based burden) 2,559 European ancestry cases, 384,798 European ancestry controls NA Illumina [185336] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90084783 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - minutes per week for walking (UKB data field 22037) 349,393 European ancestry individuals NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078857 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R13: Aphagia and dysphagia (Gene-based burden) 9,014 European ancestry cases, 376,259 European ancestry controls NA Illumina [185284] 0 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST90084786 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Summed Metabolic Equivalent Task - minutes per week for all activity (UKB data field 22040) 349,393 European ancestry individuals NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078859 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R13.1: Dysphagia (Gene-based burden) 843 European ancestry cases, 383,673 European ancestry controls NA Illumina [185265] 0 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST90084785 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - Summed minutes activity (UKB data field 22034) 349,393 European ancestry individuals NA Affymetrix, Illumina [476405] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078854 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R13.10: Dysphagia, unspecified (Gene-based burden) 840 European ancestry cases, 383,714 European ancestry controls NA Illumina [185266] 0 Dysphagia http://purl.obolibrary.org/obo/HP_0002015 GCST90084784 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Metabolic Equivalent Task - Above moderate/vigorous walking recommendation (UKB data field 22036) 285,477 European ancestry cases, 63,838 European ancestry controls NA Affymetrix, Illumina [476331] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90078856 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R14: Flatulence and related conditions (Gene-based burden) 3,601 European ancestry cases, 378,807 European ancestry controls NA Illumina [185245] 0 flatulence http://www.ebi.ac.uk/efo/EFO_0009669 GCST90084788 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z71: Persons encountering health services for other counseling and medical advice, not elsewhere classified 58,197 European ancestry cases, 290,856 European ancestry controls NA Affymetrix, Illumina [475583] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081309 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R14.0: Abdominal distension (gaseous) (Gene-based burden) 782 European ancestry cases, 384,049 European ancestry controls NA Illumina [185273] 0 flatulence http://www.ebi.ac.uk/efo/EFO_0009669 GCST90084787 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: Other joint disorder, not elsewhere classified 46,051 European ancestry cases, 302,113 European ancestry controls NA Affymetrix, Illumina [474871] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90080466 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R15: Fecal incontinence (Gene-based burden) 2,597 European ancestry cases, 384,604 European ancestry controls NA Illumina [185336] 0 fecal incontinence http://www.ebi.ac.uk/efo/EFO_0009523 GCST90084789 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z40: Encounter for prophylactic surgery 40,136 European ancestry cases, 307,162 European ancestry controls NA Affymetrix, Illumina [474306] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081254 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R16: Hepatomegaly and splenomegaly, not elsewhere classified (Gene-based burden) 864 European ancestry cases, 386,770 European ancestry controls NA Illumina [185341] 0 Hepatomegaly, Splenomegaly http://purl.obolibrary.org/obo/HP_0002240, http://purl.obolibrary.org/obo/HP_0001744 GCST90084791 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interpolated Age of participant when operation took place (UKB data field 20011) 346,023 European ancestry individuals NA Affymetrix, Illumina [472996] 1 medical procedure, age at onset http://www.ebi.ac.uk/efo/EFO_0002571, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90078244 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R16.1: Splenomegaly, not elsewhere classified (Gene-based burden) 515 European ancestry cases, 387,283 European ancestry controls NA Illumina [185343] 0 Splenomegaly http://purl.obolibrary.org/obo/HP_0001744 GCST90084790 Exome-wide sequencing 2021-08-26 33740106 Liu YQ 2021-03-19 Calcif Tissue Int www.ncbi.nlm.nih.gov/pubmed/33740106 Identification of Novel Pleiotropic SNPs Associated with Osteoporosis and Rheumatoid Arthritis. Total body bone mineral density or rheumatoid arthritis (pleiotropy) 66,628 European ancestry individuals with bone mineral density measurement, 58,284 European ancestry individuals with rheumatoid arthritis NA NR [464637] 0 rheumatoid arthritis, bone density http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0003923 GCST012243 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Disc degeneration 1,059 European ancestry cases, 330,695 European ancestry controls NA Affymetrix, Illumina [458873] 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST90077921 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41.3: Other amnesia (Gene-based burden) 1,813 European ancestry cases, 383,312 European ancestry controls NA Illumina [185305] 0 amnesia http://www.ebi.ac.uk/efo/EFO_1001454 GCST90084841 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diverticular disease diverticulitis 5,370 European ancestry cases, 326,384 European ancestry controls NA Affymetrix, Illumina [458873] 0 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90077863 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41.8: Other symptoms and signs involving cognitive functions and awareness (Gene-based burden) 929 European ancestry cases, 385,683 European ancestry controls NA Illumina [185324] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90084842 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Dry eyes 1,085 European ancestry cases, 330,669 European ancestry controls NA Affymetrix, Illumina [458873] 0 dry eye syndrome http://www.ebi.ac.uk/efo/EFO_1000906 GCST90077918 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R42: Dizziness and giddiness (Gene-based burden) 14,711 European ancestry cases, 356,152 European ancestry controls NA Illumina [185123] 0 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90084844 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duodenal ulcer 1,872 European ancestry cases, 329,882 European ancestry controls NA Affymetrix, Illumina [458873] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90077861 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R44: Other symptoms and signs involving general sensations and perceptions (Gene-based burden) 1,374 European ancestry cases, 383,396 European ancestry controls NA Illumina [185293] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90084845 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Dyspepsia indigestion 836 European ancestry cases, 330,918 European ancestry controls NA Affymetrix, Illumina [458873] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90077909 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R45: Symptoms and signs involving emotional state (Gene-based burden) 2,300 European ancestry cases, 380,293 European ancestry controls NA Illumina [185249] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90084847 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ear vestibular disorder 3,950 European ancestry cases, 327,804 European ancestry controls NA Affymetrix, Illumina [458873] 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90077834 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R45.8: Other symptoms and signs involving emotional state (Gene-based burden) 1,457 European ancestry cases, 382,413 European ancestry controls NA Illumina [185279] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90084846 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eczema or dermatitis 12,790 European ancestry cases, 318,964 European ancestry controls NA Affymetrix, Illumina [458873] 1 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90077853 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R47: Speech disturbances, not elsewhere classified (Gene-based burden) 2,139 European ancestry cases, 385,206 European ancestry controls NA Illumina [185330] 0 Speech apraxia http://purl.obolibrary.org/obo/HP_0011098 GCST90084850 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Emphysema chronic bronchitis 6,252 European ancestry cases, 325,502 European ancestry controls NA Affymetrix, Illumina [458873] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90077675 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R47.0: Dysphasia and aphasia (Gene-based burden) 948 European ancestry cases, 386,838 European ancestry controls NA Illumina [185341] 0 specific language disorder http://purl.obolibrary.org/obo/MONDO_0016226 GCST90084848 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Epilepsy 3,591 European ancestry cases, 328,163 European ancestry controls NA Affymetrix, Illumina [458873] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90077743 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R47.8: Other speech disturbances (Gene-based burden) 999 European ancestry cases, 386,616 European ancestry controls NA Illumina [185334] 0 specific language disorder http://purl.obolibrary.org/obo/MONDO_0016226 GCST90084849 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Essential hypertension 2,954 European ancestry cases, 328,800 European ancestry controls NA Affymetrix, Illumina [458873] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90077651 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R49: Voice and resonance disorders (Gene-based burden) 2,270 European ancestry cases, 381,451 European ancestry controls NA Illumina [185286] 0 voice disorders http://www.ebi.ac.uk/efo/EFO_0009692 GCST90084853 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye or eyelid problem 3,583 European ancestry cases, 328,171 European ancestry controls NA Affymetrix, Illumina [458873] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90077732 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R49.0: Dysphonia (Gene-based burden) 1,188 European ancestry cases, 385,932 European ancestry controls NA Illumina [185331] 0 voice disorders http://www.ebi.ac.uk/efo/EFO_0009692 GCST90084851 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fibromyalgia 854 European ancestry cases, 330,900 European ancestry controls NA Affymetrix, Illumina [458873] 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90077931 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R49.8: Other voice and resonance disorders (Gene-based burden) 1,104 European ancestry cases, 383,346 European ancestry controls NA Illumina [185296] 0 voice disorders http://www.ebi.ac.uk/efo/EFO_0009692 GCST90084852 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture clavicle collar bone 739 European ancestry cases, 331,015 European ancestry controls NA Affymetrix, Illumina [458873] 0 clavicle fracture http://www.ebi.ac.uk/efo/EFO_0009614 GCST90077966 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R32: Unspecified urinary incontinence (Gene-based burden) 4,119 European ancestry cases, 380,440 European ancestry controls NA Illumina [185255] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90084829 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chickenpox 7,564 European ancestry cases, 324,190 European ancestry controls NA Affymetrix, Illumina [458873] 0 chickenpox http://www.ebi.ac.uk/efo/EFO_0007204 GCST90077947 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R33: Retention of urine (Gene-based burden) 9,413 European ancestry cases, 377,878 European ancestry controls NA Illumina [185335] 0 Urinary retention http://purl.obolibrary.org/obo/HP_0000016 GCST90084830 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cholelithiasis or gall stones 7,669 European ancestry cases, 324,085 European ancestry controls 7,076 European ancestry cases, 108,108 European ancestry controls Affymetrix, Illumina [458873] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90077704 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R35: Polyuria (Gene-based burden) 7,550 European ancestry cases, 369,997 European ancestry controls NA Illumina [185179] 0 Polyuria http://purl.obolibrary.org/obo/HP_0000103 GCST90084833 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic fatigue syndrome 2,009 European ancestry cases, 329,745 European ancestry controls NA Affymetrix, Illumina [458873] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90077895 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R35.0: Frequency of micturition (Gene-based burden) 1,384 European ancestry cases, 381,947 European ancestry controls NA Illumina [185263] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90084831 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive airways disease copd 1,758 European ancestry cases, 329,996 European ancestry controls NA Affymetrix, Illumina [458873] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90077673 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R35.1: Nocturia (Gene-based burden) 931 European ancestry cases, 383,625 European ancestry controls NA Illumina [185301] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90084832 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic sinusitis 3,481 European ancestry cases, 328,273 European ancestry controls NA Affymetrix, Illumina [458873] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90077836 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39: Other and unspecified symptoms and signs involving the genitourinary system (Gene-based burden) 9,404 European ancestry cases, 367,195 European ancestry controls NA Illumina [185174] 0 Abnormality of the urinary system http://purl.obolibrary.org/obo/HP_0000079 GCST90084838 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Colitis not crohns or ulcerative colitis 1,203 European ancestry cases, 330,551 European ancestry controls NA Affymetrix, Illumina [458873] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90077865 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.1: Other difficulties with micturition (Gene-based burden) 2,813 European ancestry cases, 381,615 European ancestry controls NA Illumina [185280] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90084835 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Constipation 601 European ancestry cases, 331,153 European ancestry controls NA Affymetrix, Illumina [458873] 0 Constipation http://purl.obolibrary.org/obo/HP_0002019 GCST90077957 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.15: Urgency of urination (Gene-based burden) 588 European ancestry cases, 384,738 European ancestry controls NA Illumina [185293] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90084834 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Crohns disease 1,324 European ancestry cases, 330,430 European ancestry controls NA Affymetrix, Illumina [458873] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90077869 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.8: Other symptoms and signs involving the genitourinary system (Gene-based burden) 3,897 European ancestry cases, 383,861 European ancestry controls NA Illumina [185343] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90084836 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Deep venous thrombosis 8,947 European ancestry cases, 322,807 European ancestry controls NA Affymetrix, Illumina [458873] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90077669 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.9: Unspecified symptoms and signs involving the genitourinary system (Gene-based burden) 2,149 European ancestry cases, 379,294 European ancestry controls NA Illumina [185253] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90084837 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression 27,241 European ancestry cases, 304,513 European ancestry controls NA Affymetrix, Illumina [458873] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90077761 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R40: Somnolence, stupor and coma (Gene-based burden) 1,017 European ancestry cases, 386,284 European ancestry controls NA Illumina [185340] 0 Coma http://purl.obolibrary.org/obo/HP_0001259 GCST90084839 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetes 17,927 European ancestry cases, 313,827 European ancestry controls NA Affymetrix, Illumina [458873] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90077722 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41: Other symptoms and signs involving cognitive functions and awareness (Gene-based burden) 5,710 European ancestry cases, 378,069 European ancestry controls NA Illumina [185282] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90084843 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetic eye disease 995 European ancestry cases, 330,759 European ancestry controls NA Affymetrix, Illumina [458873] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90077752 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41.0: Disorientation, unspecified (Gene-based burden) 3,254 European ancestry cases, 384,332 European ancestry controls NA Illumina [185339] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90084840 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R50: Fever of other and unknown origin (Gene-based burden) 6,970 European ancestry cases, 373,504 European ancestry controls NA Illumina [185223] 0 fever of unknown origin http://www.ebi.ac.uk/efo/EFO_0003952 GCST90084855 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture fibula 661 European ancestry cases, 331,093 European ancestry controls NA Affymetrix, Illumina [458873] 0 fibula fracture http://www.ebi.ac.uk/efo/EFO_0009613 GCST90077982 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R50.9: Fever, unspecified (Gene-based burden) 6,471 European ancestry cases, 373,978 European ancestry controls NA Illumina [185223] 0 fever of unknown origin http://www.ebi.ac.uk/efo/EFO_0003952 GCST90084854 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture finger 798 European ancestry cases, 330,956 European ancestry controls NA Affymetrix, Illumina [458873] 0 finger fracture http://www.ebi.ac.uk/efo/EFO_0009616 GCST90077974 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R51: Headache (Gene-based burden) 17,773 European ancestry cases, 353,610 European ancestry controls NA Illumina [185094] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90084856 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture of forearm or wrist 1,206 European ancestry cases, 330,548 European ancestry controls NA Affymetrix, Illumina [458873] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90077970 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R52: Pain, unspecified (Gene-based burden) 6,438 European ancestry cases, 369,102 European ancestry controls NA Illumina [185109] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90084859 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture lower leg ankle 2,253 European ancestry cases, 329,501 European ancestry controls NA Affymetrix, Illumina [458873] 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90077978 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R52.1: Chronic intractable pain (Gene-based burden) 868 European ancestry cases, 387,062 European ancestry controls NA Illumina [185344] 0 Chronic pain http://purl.obolibrary.org/obo/HP_0012532 GCST90084857 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture nose 744 European ancestry cases, 331,010 European ancestry controls NA Affymetrix, Illumina [458873] 0 nose injury http://www.ebi.ac.uk/efo/EFO_0009623 GCST90077964 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R52.2: Other chronic pain (Gene-based burden) 509 European ancestry cases, 387,421 European ancestry controls NA Illumina [185344] 0 Chronic pain http://purl.obolibrary.org/obo/HP_0012532 GCST90084858 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture rib 651 European ancestry cases, 331,103 European ancestry controls NA Affymetrix, Illumina [458873] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90077976 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53: Malaise and fatigue (Gene-based burden) 11,044 European ancestry cases, 358,086 European ancestry controls NA Illumina [185060] 0 malaise, Fatigue http://www.ebi.ac.uk/efo/EFO_0009641, http://purl.obolibrary.org/obo/HP_0012378 GCST90084864 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture tibia 693 European ancestry cases, 331,061 European ancestry controls NA Affymetrix, Illumina [458873] 0 tibia fracture http://www.ebi.ac.uk/efo/EFO_0003944 GCST90077980 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.8: Other malaise and fatigue (Gene-based burden) 6,340 European ancestry cases, 365,215 European ancestry controls NA Illumina [185106] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90084863 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture toe 557 European ancestry cases, 331,197 European ancestry controls NA Affymetrix, Illumina [458873] 0 foot fracture http://www.ebi.ac.uk/efo/EFO_0009618 GCST90077984 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.81: Other malaise (Gene-based burden) 670 European ancestry cases, 383,920 European ancestry controls NA Illumina [185298] 0 malaise http://www.ebi.ac.uk/efo/EFO_0009641 GCST90084860 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture upper arm humerus elbow 1,286 European ancestry cases, 330,468 European ancestry controls NA Affymetrix, Illumina [458873] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90077968 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.82: Chronic fatigue, unspecified (Gene-based burden) 4,932 European ancestry cases, 372,337 European ancestry controls NA Illumina [185180] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90084861 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture wrist colles fracture 1,658 European ancestry cases, 330,096 European ancestry controls NA Affymetrix, Illumina [458873] 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90077972 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.83: Other fatigue (Gene-based burden) 938 European ancestry cases, 382,816 European ancestry controls NA Illumina [185279] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90084862 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gastritis gastric erosions 836 European ancestry cases, 330,918 European ancestry controls NA Affymetrix, Illumina [458873] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90077697 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R54: Age-related physical debility (Gene-based burden) 756 European ancestry cases, 386,430 European ancestry controls NA Illumina [185314] 0 functional decline measurement http://www.ebi.ac.uk/efo/EFO_0007784 GCST90084865 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gastro oesophageal reflux or gastric reflux 21,143 European ancestry cases, 310,611 European ancestry controls NA Affymetrix, Illumina [458873] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90077692 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R55: Syncope and collapse (Gene-based burden) 12,288 European ancestry cases, 370,934 European ancestry controls NA Illumina [185288] 0 Syncope http://purl.obolibrary.org/obo/HP_0001279 GCST90084866 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glaucoma 5,059 European ancestry cases, 326,695 European ancestry controls 8,012 European ancestry cases, 113,883 European ancestry controls Affymetrix, Illumina [458873] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90077754 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R56: Convulsions, not elsewhere classified (Gene-based burden) 2,932 European ancestry cases, 384,060 European ancestry controls NA Illumina [185332] 0 Seizure http://purl.obolibrary.org/obo/HP_0001250 GCST90084869 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gout 6,554 European ancestry cases, 325,200 European ancestry controls NA Affymetrix, Illumina [458873] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90077877 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R56.8: Other and unspecified convulsions (Gene-based burden) 2,538 European ancestry cases, 385,392 European ancestry controls NA Illumina [185344] 0 Seizure http://purl.obolibrary.org/obo/HP_0001250 GCST90084867 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Haemorrhoids piles 1,601 European ancestry cases, 330,153 European ancestry controls NA Affymetrix, Illumina [458873] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90077905 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R56.9: Unspecified convulsions (Gene-based burden) 543 European ancestry cases, 386,355 European ancestry controls NA Illumina [185333] 0 convulsion http://www.ebi.ac.uk/efo/EFO_0009853 GCST90084868 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hayfever allergic rhinitis 27,391 European ancestry cases, 304,363 European ancestry controls NA Affymetrix, Illumina [458873] 0 allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0005854 GCST90077815 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R57: Shock, not elsewhere classified (Gene-based burden) 541 European ancestry cases, 387,377 European ancestry controls NA Illumina [185344] 0 Shock http://purl.obolibrary.org/obo/HP_0031273 GCST90084870 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Head injury 1,488 European ancestry cases, 330,266 European ancestry controls NA Affymetrix, Illumina [458873] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90077747 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R59: Enlarged lymph nodes (Gene-based burden) 3,668 European ancestry cases, 380,619 European ancestry controls NA Illumina [185280] 0 Lymphadenopathy http://purl.obolibrary.org/obo/HP_0002716 GCST90084873 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Headaches (not migraine) 3,962 European ancestry cases, 327,792 European ancestry controls NA Affymetrix, Illumina [458873] 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90077844 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R59.0: Localized enlarged lymph nodes (Gene-based burden) 2,468 European ancestry cases, 384,030 European ancestry controls NA Illumina [185309] 0 Lymphadenopathy http://purl.obolibrary.org/obo/HP_0002716 GCST90084871 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart arrhythmia 2,496 European ancestry cases, 329,258 European ancestry controls NA Affymetrix, Illumina [458873] 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90077659 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R59.1: Generalized enlarged lymph nodes (Gene-based burden) 998 European ancestry cases, 384,487 European ancestry controls NA Illumina [185308] 0 Lymphadenopathy http://purl.obolibrary.org/obo/HP_0002716 GCST90084872 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart attack myocardial infarction 10,448 European ancestry cases, 321,306 European ancestry controls NA Affymetrix, Illumina [458873] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90077657 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R60: Edema, not elsewhere classified (Gene-based burden) 5,259 European ancestry cases, 374,500 European ancestry controls NA Illumina [185207] 0 edema http://www.ebi.ac.uk/efo/EFO_0009373 GCST90084876 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart cardiac problem 1,496 European ancestry cases, 330,258 European ancestry controls NA Affymetrix, Illumina [458873] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90077647 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R60.0: Localized edema (Gene-based burden) 2,631 European ancestry cases, 382,554 European ancestry controls NA Illumina [185301] 0 edema http://www.ebi.ac.uk/efo/EFO_0009373 GCST90084874 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart valve problem or heart murmur 3,129 European ancestry cases, 328,625 European ancestry controls NA Affymetrix, Illumina [458873] 0 Abnormal cardiovascular system physiology http://purl.obolibrary.org/obo/HP_0011025 GCST90077661 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R60.9: Edema, unspecified (Gene-based burden) 2,772 European ancestry cases, 378,986 European ancestry controls NA Illumina [185239] 0 edema http://www.ebi.ac.uk/efo/EFO_0009373 GCST90084875 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Helicobacter pylori 1,375 European ancestry cases, 330,379 European ancestry controls NA Affymetrix, Illumina [458873] 0 Helicobacter pylori http://purl.obolibrary.org/obo/NCBITaxon_210 GCST90077849 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R61: Generalized hyperhidrosis (Gene-based burden) 1,491 European ancestry cases, 383,413 European ancestry controls NA Illumina [185315] 0 Hyperhidrosis http://purl.obolibrary.org/obo/HP_0000975 GCST90084878 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hepatitis 506 European ancestry cases, 331,248 European ancestry controls NA Affymetrix, Illumina [458873] 0 Hepatitis http://purl.obolibrary.org/obo/HP_0012115 GCST90077701 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R61.9: Hyperhidrosis, unspecified (Gene-based burden) 713 European ancestry cases, 387,217 European ancestry controls NA Illumina [185344] 0 Hyperhidrosis http://purl.obolibrary.org/obo/HP_0000975 GCST90084877 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hiatus hernia 10,744 European ancestry cases, 321,010 European ancestry controls NA Affymetrix, Illumina [458873] 0 Hiatus hernia http://purl.obolibrary.org/obo/HP_0002036 GCST90077885 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2021-07-13 33232597 Kong SH 2020-11-24 Endocrinol Metab (Seoul) www.ncbi.nlm.nih.gov/pubmed/33232597 Identification of Novel Genetic Variants Related to Trabecular Bone Score in Community-Dwelling Older Adults. trabecular bone score 2,451 Korean ancestry individuals 2,733 Korean ancestry individuals Affymetrix [1418709] (imputed) 0 trabecular bone score http://www.ebi.ac.uk/efo/EFO_0600018 GCST012025 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61: Open wound of wrist, hand and fingers (Gene-based burden) 4,118 European ancestry cases, 381,007 European ancestry controls NA Illumina [185306] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084983 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Uterine fibroids 7,143 European ancestry cases, 324,611 European ancestry controls NA Affymetrix, Illumina [458855] 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90077796 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.0: Open wound of thumb without damage to nail (Gene-based burden) 2,186 European ancestry cases, 385,319 European ancestry controls NA Illumina [185329] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084979 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Enlarged prostate 7,026 European ancestry cases, 324,728 European ancestry controls NA Affymetrix, Illumina [458827] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90077817 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.1: Open wound of thumb with damage to nail (Gene-based burden) 563 European ancestry cases, 387,356 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084980 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gestational hypertension pre eclampsia 1,789 European ancestry cases, 329,965 European ancestry controls NA Affymetrix, Illumina [458672] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90077653 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.8: Open wound of other parts of wrist and hand (S61.8) (Gene-based burden) 645 European ancestry cases, 387,285 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084981 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Abnormal smear cervix 735 European ancestry cases, 331,019 European ancestry controls NA Affymetrix, Illumina [458564] 0 abnormal PAP smear http://www.ebi.ac.uk/efo/EFO_0009511 GCST90077987 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.9: Open wound of wrist and hand part, part unspecified (S61.9) (Gene-based burden) 543 European ancestry cases, 387,387 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084982 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gynaecological disorder (not cancer) 748 European ancestry cases, 331,006 European ancestry controls NA Affymetrix, Illumina [458432] 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90077791 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62: Fracture at wrist and hand level (Gene-based burden) 3,764 European ancestry cases, 376,129 European ancestry controls NA Illumina [185235] 0 wrist fracture http://www.ebi.ac.uk/efo/EFO_0009515 GCST90084988 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Female infertility 592 European ancestry cases, 331,162 European ancestry controls NA Affymetrix, Illumina [458106] 0 female infertility http://www.ebi.ac.uk/efo/EFO_0008560 GCST90077823 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.3: Fracture of other and unspecified metacarpal bone (Gene-based burden) 736 European ancestry cases, 384,858 European ancestry controls NA Illumina [185319] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084985 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prostate problem (not cancer) 774 European ancestry cases, 330,980 European ancestry controls NA Affymetrix, Illumina [458057] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90077718 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.30: Unspecified fracture of other metacarpal bone (Gene-based burden) 613 European ancestry cases, 385,091 European ancestry controls NA Illumina [185321] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084984 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lipoprotein A levels (UKB data field 30790) 329,317 European ancestry individuals NA Affymetrix, Illumina [457460] 6 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90079034 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.6: Fracture of other and unspecified finger(s) (Gene-based burden) 1,681 European ancestry cases, 383,442 European ancestry controls NA Illumina [185309] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084987 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Polycystic ovaries polycystic ovarian syndrome 573 European ancestry cases, 331,181 European ancestry controls NA Affymetrix, Illumina [456851] 0 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST90077795 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S62.60: Fracture of unspecified phalanx of finger (Gene-based burden) 1,048 European ancestry cases, 384,698 European ancestry controls NA Illumina [185311] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084986 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease 14,114 European ancestry cases, 315,430 European ancestry controls NA Affymetrix, Illumina [456481] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90081469 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S63: Dislocation and sprain of joints and ligaments at wrist and hand level (Gene-based burden) 980 European ancestry cases, 383,792 European ancestry controls NA Illumina [185297] 0 dislocation, sprain http://www.ebi.ac.uk/efo/EFO_0009521, http://www.ebi.ac.uk/efo/EFO_0009582 GCST90084989 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma vs allergic disease 47,628 European ancestry cases, 280,686 European ancestry controls NA Affymetrix, Illumina [456404] 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90081459 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S64: Injury of nerves at wrist and hand level (Gene-based burden) 797 European ancestry cases, 387,028 European ancestry controls NA Illumina [185342] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084990 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spinal injury 730 European ancestry cases, 328,322 European ancestry controls NA Affymetrix, Illumina [456275] 0 Spinal cord injury http://www.ebi.ac.uk/efo/EFO_1001919 GCST90077749 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S66: Injury of muscle, fascia and tendon at wrist and hand level (Gene-based burden) 1,424 European ancestry cases, 386,327 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084992 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye trauma 681 European ancestry cases, 331,073 European ancestry controls NA Affymetrix, Illumina [458872] 0 eye injury http://www.ebi.ac.uk/efo/EFO_0009485 GCST90077758 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S43: Dislocation and sprain of joints and ligaments of shoulder girdle (Gene-based burden) 962 European ancestry cases, 384,037 European ancestry controls NA Illumina [185300] 0 dislocation, sprain http://www.ebi.ac.uk/efo/EFO_0009521, http://www.ebi.ac.uk/efo/EFO_0009582 GCST90084968 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Inguinal hernia 2,528 European ancestry cases, 329,226 European ancestry controls NA Affymetrix, Illumina [458872] 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90077912 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S43.0: Subluxation and dislocation of shoulder joint (Gene-based burden) 584 European ancestry cases, 386,546 European ancestry controls NA Illumina [185333] 0 dislocation, sprain http://www.ebi.ac.uk/efo/EFO_0009521, http://www.ebi.ac.uk/efo/EFO_0009582 GCST90084967 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other abdominal problem 528 European ancestry cases, 331,226 European ancestry controls NA Affymetrix, Illumina [458872] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90077691 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S51: Open wound of elbow and forearm (Gene-based burden) 609 European ancestry cases, 387,015 European ancestry controls NA Illumina [185340] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084969 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other respiratory problems 759 European ancestry cases, 330,995 European ancestry controls NA Affymetrix, Illumina [458872] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90077679 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52: Fracture of forearm (Gene-based burden) 8,168 European ancestry cases, 371,727 European ancestry controls NA Illumina [185196] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084977 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Interpolated Age of participant when non cancer illness first diagnosed (UKB data field 20009) 331,753 European ancestry individuals NA Affymetrix, Illumina [458871] 0 age at onset, disease http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0000408 GCST90078242 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.0: Fracture of upper end of ulna (Gene-based burden) 953 European ancestry cases, 386,775 European ancestry controls NA Illumina [185342] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084971 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Testicular problems (not cancer) 628 European ancestry cases, 331,126 European ancestry controls NA Affymetrix, Illumina [458871] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90077720 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.00: Unspecified fracture of upper end of ulna (Gene-based burden) 758 European ancestry cases, 387,122 European ancestry controls NA Illumina [185344] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084970 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malaria 563 European ancestry cases, 331,191 European ancestry controls NA Affymetrix, Illumina [458870] 0 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST90077848 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.1: Fracture of upper end of radius (Gene-based burden) 529 European ancestry cases, 386,599 European ancestry controls NA Illumina [185327] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084972 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Endometriosis 3,711 European ancestry cases, 328,043 European ancestry controls NA Affymetrix, Illumina [458869] 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90077821 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.5: Fracture of lower end of radius (Gene-based burden) 5,267 European ancestry cases, 379,424 European ancestry controls NA Illumina [185272] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084974 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Miscarriage 1,373 European ancestry cases, 330,381 European ancestry controls NA Affymetrix, Illumina [458869] 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90077935 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.50: Unspecified fracture of the lower end of radius (Gene-based burden) 4,489 European ancestry cases, 381,436 European ancestry controls NA Illumina [185311] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084973 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Menorrhagia unknown cause 1,559 European ancestry cases, 330,195 European ancestry controls NA Affymetrix, Illumina [458867] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90077933 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.6: Fracture of lower end of ulna (Gene-based burden) 1,019 European ancestry cases, 385,988 European ancestry controls NA Illumina [185333] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084976 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Transient ischaemic attack tia 1,877 European ancestry cases, 329,877 European ancestry controls NA Affymetrix, Illumina [458867] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90077665 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.60: Unspecified fracture of lower end of ulna (Gene-based burden) 862 European ancestry cases, 386,222 European ancestry controls NA Illumina [185333] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084975 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Benign prostatic hypertrophy 1,075 European ancestry cases, 330,679 European ancestry controls NA Affymetrix, Illumina [458860] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90077916 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S60: Superficial injury of wrist, hand and fingers (Gene-based burden) 652 European ancestry cases, 385,604 European ancestry controls NA Illumina [185322] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084978 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vaginal prolapse uterine prolapse 2,758 European ancestry cases, 328,996 European ancestry controls NA Affymetrix, Illumina [458859] 0 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90077800 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleep apnoea 1,594 European ancestry cases, 330,160 European ancestry controls NA Affymetrix, Illumina [458873] 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90077681 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S13: Dislocation and sprain of joints and ligaments at neck level (Gene-based burden) 1,078 European ancestry cases, 381,603 European ancestry controls NA Illumina [185274] 0 neck injury http://www.ebi.ac.uk/efo/EFO_0009476 GCST90084943 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spinal injury 730 European ancestry cases, 331,024 European ancestry controls NA Affymetrix, Illumina [458873] 0 Spinal cord injury http://www.ebi.ac.uk/efo/EFO_1001919 GCST90077748 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S13.4: Sprain of ligaments of cervical spine (Gene-based burden) 993 European ancestry cases, 381,714 European ancestry controls NA Illumina [185274] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084942 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spine arthritis or spondylitis 4,039 European ancestry cases, 327,715 European ancestry controls NA Affymetrix, Illumina [458873] 0 spondylitis http://purl.obolibrary.org/obo/MONDO_0003937 GCST90077781 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S20: Superficial injury of thorax (Gene-based burden) 541 European ancestry cases, 386,810 European ancestry controls NA Illumina [185322] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084944 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spontaneous pneumothorax recurrent pneumothorax 1,058 European ancestry cases, 330,696 European ancestry controls 547 European ancestry cases, 121,171 European ancestry controls Affymetrix, Illumina [458873] 0 Spontaneous pneumothorax http://purl.obolibrary.org/obo/HP_0002108 GCST90077685 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22: Fracture of rib(s), sternum and thoracic spine (Gene-based burden) 2,628 European ancestry cases, 383,401 European ancestry controls NA Illumina [185278] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90084949 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stomach disorder 974 European ancestry cases, 330,780 European ancestry controls NA Affymetrix, Illumina [458873] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90077687 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.0: Fracture of thoracic vertebra (Gene-based burden) 568 European ancestry cases, 387,032 European ancestry controls NA Illumina [185324] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084945 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stress 977 European ancestry cases, 330,777 European ancestry controls NA Affymetrix, Illumina [458873] 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90077959 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.3: Fracture of one rib (Gene-based burden) 756 European ancestry cases, 385,854 European ancestry controls NA Illumina [185306] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90084947 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stroke 6,014 European ancestry cases, 325,740 European ancestry controls NA Affymetrix, Illumina [458873] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90077663 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.30: Fracture of one rib (Gene-based burden) 512 European ancestry cases, 387,418 European ancestry controls NA Illumina [185344] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90084946 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Systemic lupus erythematosis sle 523 European ancestry cases, 331,231 European ancestry controls NA Affymetrix, Illumina [458873] 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90077810 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.4: Multiple fractures of ribs (Gene-based burden) 1,087 European ancestry cases, 386,549 European ancestry controls NA Illumina [19298] 0 multiple bone fractures http://www.ebi.ac.uk/efo/EFO_0009513 GCST90084948 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tendonitis tendinitis tenosynovitis 539 European ancestry cases, 331,215 European ancestry controls NA Affymetrix, Illumina [458873] 0 tendinitis http://purl.obolibrary.org/obo/MONDO_0004857 GCST90077963 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S27: Injury of other and unspecified intrathoracic organs (Gene-based burden) 881 European ancestry cases, 386,963 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084950 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Thyroid problem (not cancer) 1,214 European ancestry cases, 330,540 European ancestry controls NA Affymetrix, Illumina [458873] 0 thyroid disease http://www.ebi.ac.uk/efo/EFO_1000627 GCST90077726 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S30: Superficial injury of abdomen, lower back, pelvis and external genitals (Gene-based burden) 786 European ancestry cases, 386,864 European ancestry controls NA Illumina [185340] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084951 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus tiniitis 1,618 European ancestry cases, 330,136 European ancestry controls NA Affymetrix, Illumina [458873] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90077953 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32: Fracture of lumbar spine and pelvis (Gene-based burden) 1,842 European ancestry cases, 385,220 European ancestry controls NA Illumina [185330] 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90084956 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tonsiltis 5,112 European ancestry cases, 326,642 European ancestry controls NA Affymetrix, Illumina [458873] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90077955 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.0: Fracture of lumbar vertebra (Gene-based burden) 745 European ancestry cases, 386,833 European ancestry controls NA Illumina [185337] 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90084953 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trapped nerve compressed nerve 1,550 European ancestry cases, 330,204 European ancestry controls NA Affymetrix, Illumina [458873] 0 nerve compression syndrome http://www.ebi.ac.uk/efo/EFO_0009487 GCST90077737 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78: allergy hypersensitivity anaphylaxis 2,818 European ancestry cases, 326,234 European ancestry controls NA Affymetrix, Illumina [456275] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90077807 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S66.3: Injury of extensor muscle, fascia and tendon of other and unspecified finger at wrist and hand level (Gene-based burden) 531 European ancestry cases, 387,384 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084991 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T887: allergy or anaphylactic reaction to drug 4,381 European ancestry cases, 324,671 European ancestry controls NA Affymetrix, Illumina [456275] 0 drug allergy http://www.ebi.ac.uk/efo/EFO_0009482 GCST90077814 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S69: Other and unspecified injuries of wrist, hand and finger(s) (Gene-based burden) 1,200 European ancestry cases, 381,238 European ancestry controls NA Illumina [185270] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084995 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T780: allergy or anaphylactic reaction to food 2,000 European ancestry cases, 327,052 European ancestry controls NA Affymetrix, Illumina [456275] 0 food allergy http://www.ebi.ac.uk/efo/EFO_1001890 GCST90077812 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S69.9: Unspecified injury of wrist, hand and finger(s) (Gene-based burden) 1,134 European ancestry cases, 381,363 European ancestry controls NA Illumina [185275] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084994 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D64: anaemia 900 European ancestry cases, 328,152 European ancestry controls NA Affymetrix, Illumina [456275] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90077852 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S69.90: Unspecified injury of unspecified wrist, hand and finger(s) (Gene-based burden) 937 European ancestry cases, 381,550 European ancestry controls NA Illumina [185275] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084993 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20: angina 13,585 European ancestry cases, 315,467 European ancestry controls NA Affymetrix, Illumina [456275] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90077656 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72: Fracture of femur (Gene-based burden) 3,054 European ancestry cases, 384,117 European ancestry controls NA Illumina [185333] 0 femur fracture http://www.ebi.ac.uk/efo/EFO_0008553 GCST90084999 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M45: ankylosing spondylitis 1,113 European ancestry cases, 327,939 European ancestry controls NA Affymetrix, Illumina [456275] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90077786 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72.0: Fracture of head and neck of femur (Gene-based burden) 1,990 European ancestry cases, 385,682 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084997 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41: Anxiety or panic attacks 5,864 European ancestry cases, 323,188 European ancestry controls NA Affymetrix, Illumina [456275] 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90077764 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72.00: Fracture of unspecified part of neck of femur (Gene-based burden) 1,793 European ancestry cases, 385,858 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084996 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K37: appendicitis 4,175 European ancestry cases, 324,877 European ancestry controls NA Affymetrix, Illumina [456275] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90077904 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72.1: Pertrochanteric fracture (Gene-based burden) 535 European ancestry cases, 387,361 European ancestry controls NA Illumina [185342] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084998 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13: arthritis nos 4,546 European ancestry cases, 324,506 European ancestry controls NA Affymetrix, Illumina [456275] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90077928 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S76: Injury of muscle, fascia and tendon at hip and thigh level (Gene-based burden) 547 European ancestry cases, 386,228 European ancestry controls NA Illumina [185312] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085000 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I48: atrial fibrillation 3,763 European ancestry cases, 325,289 European ancestry controls NA Affymetrix, Illumina [456275] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90077882 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S80: Superficial injury of knee and lower leg (Gene-based burden) 1,159 European ancestry cases, 385,152 European ancestry controls NA Illumina [185322] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085002 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: back pain 3,099 European ancestry cases, 325,953 European ancestry controls NA Affymetrix, Illumina [456275] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90077924 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S80.9: Unspecified superficial injury of knee and lower leg (Gene-based burden) 532 European ancestry cases, 387,297 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085001 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: back problem 6,409 European ancestry cases, 322,643 European ancestry controls NA Affymetrix, Illumina [456275] 0 Abnormality of the cervical spine http://purl.obolibrary.org/obo/HP_0003319 GCST90077772 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S81: Open wound of knee and lower leg (Gene-based burden) 894 European ancestry cases, 386,190 European ancestry controls NA Illumina [185332] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90085003 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32: bladder problem (not cancer) 2,606 European ancestry cases, 326,446 European ancestry controls NA Affymetrix, Illumina [456275] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90077715 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.00: Fracture of unspecified lumbar vertebra (Gene-based burden) 643 European ancestry cases, 386,917 European ancestry controls NA Illumina [185337] 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90084952 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tuberculosis tb 2,209 European ancestry cases, 329,545 European ancestry controls NA Affymetrix, Illumina [458873] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90077846 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.5: Fracture of pubis (Gene-based burden) 662 European ancestry cases, 387,126 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084955 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes 3,497 European ancestry cases, 328,257 European ancestry controls NA Affymetrix, Illumina [458873] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90077724 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.50: Unspecified fracture of pubis (Gene-based burden) 578 European ancestry cases, 387,277 European ancestry controls NA Illumina [185343] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084954 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ulcerative colitis 2,363 European ancestry cases, 329,391 European ancestry controls NA Affymetrix, Illumina [458873] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90077871 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S33: Dislocation and sprain of joints and ligaments of lumbar spine and pelvis (Gene-based burden) 1,020 European ancestry cases, 380,769 European ancestry controls NA Illumina [185245] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084958 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Umbilical hernia 521 European ancestry cases, 331,233 European ancestry controls NA Affymetrix, Illumina [458873] 0 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90077911 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S33.5: Sprain of ligaments of lumbar spine (Gene-based burden) 701 European ancestry cases, 383,115 European ancestry controls NA Illumina [185288] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084957 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urinary frequency incontinence 2,619 European ancestry cases, 329,135 European ancestry controls NA Affymetrix, Illumina [458873] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90077716 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S39: Other and unspecified injuries of abdomen, lower back, pelvis and external genitals (Gene-based burden) 574 European ancestry cases, 385,098 European ancestry controls NA Illumina [185311] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084959 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urinary tract infection or kidney infection 2,380 European ancestry cases, 329,374 European ancestry controls NA Affymetrix, Illumina [458873] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90077710 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42: Fracture of shoulder and upper arm (Gene-based burden) 3,861 European ancestry cases, 378,909 European ancestry controls NA Illumina [185269] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084966 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Uterine polyps 1,439 European ancestry cases, 330,315 European ancestry controls NA Affymetrix, Illumina [458873] 0 uterine polyp http://www.ebi.ac.uk/efo/EFO_0009484 GCST90077798 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.0: Fracture of clavicle (Gene-based burden) 1,184 European ancestry cases, 384,507 European ancestry controls NA Illumina [185309] 0 clavicle fracture http://www.ebi.ac.uk/efo/EFO_0009614 GCST90084961 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Varicose veins 2,152 European ancestry cases, 329,602 European ancestry controls NA Affymetrix, Illumina [458873] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90077899 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.00: Fracture of unspecified part of clavicle (Gene-based burden) 1,037 European ancestry cases, 384,849 European ancestry controls NA Illumina [185310] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084960 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vertigo 818 European ancestry cases, 330,936 European ancestry controls NA Affymetrix, Illumina [458873] 0 Vertigo http://purl.obolibrary.org/obo/HP_0002321 GCST90077901 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.2: Fracture of upper end of humerus (Gene-based burden) 1,432 European ancestry cases, 385,935 European ancestry controls NA Illumina [185338] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084963 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Whooping cough pertussis 1,336 European ancestry cases, 330,418 European ancestry controls NA Affymetrix, Illumina [458873] 0 whooping cough http://www.ebi.ac.uk/efo/EFO_0000650 GCST90077949 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.20: Unspecified fracture of upper end of humerus (Gene-based burden) 1,247 European ancestry cases, 386,325 European ancestry controls NA Illumina [185336] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084962 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alcohol dependency 671 European ancestry cases, 331,083 European ancestry controls NA Affymetrix, Illumina [458872] 0 alcohol dependence http://purl.obolibrary.org/obo/MONDO_0007079 GCST90077828 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.3: Fracture of shaft of humerus (Gene-based burden) 637 European ancestry cases, 385,560 European ancestry controls NA Illumina [185311] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084965 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cystitis 661 European ancestry cases, 331,093 European ancestry controls NA Affymetrix, Illumina [458872] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90077914 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.30: Unspecified fracture of shaft of humerus (Gene-based burden) 575 European ancestry cases, 385,607 European ancestry controls NA Illumina [185311] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084964 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S01.0: Open wound of scalp (Gene-based burden) 1,032 European ancestry cases, 386,667 European ancestry controls NA Illumina [185341] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084928 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Raynauds phenomenon disease 628 European ancestry cases, 331,126 European ancestry controls NA Affymetrix, Illumina [458873] 0 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90077937 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S01.8: Open wound of other parts of head (Gene-based burden) 1,527 European ancestry cases, 386,076 European ancestry controls NA Illumina [185341] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084929 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rectal or colon adenoma polyps 1,530 European ancestry cases, 330,224 European ancestry controls NA Affymetrix, Illumina [458873] 0 adenomatous colon polyp http://www.ebi.ac.uk/efo/EFO_1000633 GCST90077867 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02: Fracture of skull and facial bones (Gene-based burden) 2,601 European ancestry cases, 382,658 European ancestry controls NA Illumina [185298] 0 Skull Fractures http://www.ebi.ac.uk/efo/EFO_1001425 GCST90084935 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Retinal detachment 1,666 European ancestry cases, 330,088 European ancestry controls NA Affymetrix, Illumina [458873] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90077759 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.2: Fracture of nasal bones (Gene-based burden) 800 European ancestry cases, 385,730 European ancestry controls NA Illumina [185318] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084932 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Retinal problem 798 European ancestry cases, 330,956 European ancestry controls NA Affymetrix, Illumina [458873] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90077750 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.20: Fracture of nasal bones (Gene-based burden) 560 European ancestry cases, 387,370 European ancestry controls NA Illumina [185344] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90084931 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rheumatic fever 1,372 European ancestry cases, 330,382 European ancestry controls NA Affymetrix, Illumina [458873] 0 rheumatic fever http://www.ebi.ac.uk/efo/EFO_1001160 GCST90077893 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.4: Fracture of malar, maxillary and zygoma bones (Gene-based burden) 619 European ancestry cases, 386,946 European ancestry controls NA Illumina [185340] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084934 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rheumatoid arthritis 5,095 European ancestry cases, 326,659 European ancestry controls NA Affymetrix, Illumina [458873] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90077873 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.40: Fracture of malar, maxillary and zygoma bones, unspecified (Gene-based burden) 505 European ancestry cases, 387,096 European ancestry controls NA Illumina [185340] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084933 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rosacea 984 European ancestry cases, 330,770 European ancestry controls NA Affymetrix, Illumina [458873] 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90077985 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S05: Injury of eye and orbit (Gene-based burden) 662 European ancestry cases, 384,363 European ancestry controls NA Illumina [185310] 0 eye injury http://www.ebi.ac.uk/efo/EFO_0009485 GCST90084936 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Rubella german measles 2,248 European ancestry cases, 329,506 European ancestry controls NA Affymetrix, Illumina [458873] 0 rubella http://www.ebi.ac.uk/efo/EFO_1002026 GCST90077945 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S06: Intracranial injury (Gene-based burden) 1,553 European ancestry cases, 385,423 European ancestry controls NA Illumina [185337] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90084938 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sarcoidosis 898 European ancestry cases, 330,856 European ancestry controls NA Affymetrix, Illumina [458873] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90077804 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S06.5: Traumatic subdural hemorrhage (Gene-based burden) 540 European ancestry cases, 387,371 European ancestry controls NA Illumina [185344] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084937 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Scarlet fever scarlatina 1,058 European ancestry cases, 330,696 European ancestry controls NA Affymetrix, Illumina [458873] 0 scarlet fever http://www.ebi.ac.uk/efo/EFO_0007477 GCST90077992 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S09: Other and unspecified injuries of head (Gene-based burden) 3,584 European ancestry cases, 377,427 European ancestry controls NA Illumina [185228] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90084941 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sciatica 4,982 European ancestry cases, 326,772 European ancestry controls NA Affymetrix, Illumina [458873] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90077887 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S09.9: Unspecified injury of face and head (Gene-based burden) 3,457 European ancestry cases, 377,561 European ancestry controls NA Illumina [185228] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90084940 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Shingles 1,180 European ancestry cases, 330,574 European ancestry controls NA Affymetrix, Illumina [458873] 0 susceptibility to shingles measurement http://www.ebi.ac.uk/efo/EFO_0008401 GCST90077951 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S09.92: Unspecified injury of nose (Gene-based burden) 657 European ancestry cases, 384,430 European ancestry controls NA Illumina [185315] 0 nose injury http://www.ebi.ac.uk/efo/EFO_0009623 GCST90084939 Exome-wide sequencing 2019-03-28 30718733 Moon S 2019-02-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30718733 The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. Triglyceride levels 6,949 Korean ancestry individuals 6,000 Korean ancestry individuals Affymetrix [at least 805769] (imputed) 11 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST007437 Genome-wide genotyping array 2019-03-28 30718733 Moon S 2019-02-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30718733 The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. Low density lipoprotein cholesterol levels 6,949 Korean ancestry individuals 6,000 Korean ancestry individuals Affymetrix [at least 805769] (imputed) 8 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST007442 Genome-wide genotyping array 2019-03-28 30718733 Moon S 2019-02-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30718733 The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. High density lipoprotein cholesterol levels 6,949 Korean ancestry individuals 6,000 Korean ancestry individuals Affymetrix [at least 805769] (imputed) 17 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST007438 Genome-wide genotyping array 2019-03-28 30718733 Moon S 2019-02-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30718733 The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. Total cholesterol levels 6,949 Korean ancestry individuals 6,000 Korean ancestry individuals Affymetrix [at least 805769] (imputed) 10 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST007441 Genome-wide genotyping array 2019-03-28 30718733 Moon S 2019-02-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30718733 The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. Aspartate aminotransferase levels 6,949 Korean ancestry individuals 6,000 Korean ancestry individuals Affymetrix [at least 805769] (imputed) 4 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST007439 Genome-wide genotyping array 2019-03-28 30718733 Moon S 2019-02-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30718733 The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits. Alanine aminotransferase levels 6,949 Korean ancestry individuals 6,000 Korean ancestry individuals Affymetrix [at least 805769] (imputed) 5 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST007440 Genome-wide genotyping array 2021-08-13 33632354 Suzuki T 2021-02-26 Br J Nutr www.ncbi.nlm.nih.gov/pubmed/33632354 A Genome-wide Association Study on Confection Consumption in a Japanese Population- The Japan Multi-Institutional Collaborative Cohort study. Confectionary intake 14,073 Japanese ancestry individuals NA Illumina [8504983] (imputed) 3 energy intake http://www.ebi.ac.uk/efo/EFO_0003939 GCST012177 Genome-wide genotyping array 2021-06-23 33625064 Cindi Z 2021-02-17 J Acquir Immune Defic Syndr www.ncbi.nlm.nih.gov/pubmed/33625064 Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens. Response to dolutegravir (body weight gain) 314 Black South African individuals NA Illumina [NR] (imputed) 2 response to reverse transcriptase inhibitor, response to dolutegravir, body weight gain http://purl.obolibrary.org/obo/GO_0061479, http://www.ebi.ac.uk/efo/EFO_0600017, http://www.ebi.ac.uk/efo/EFO_0004566 GCST011960 Genome-wide genotyping array 2021-06-23 33625064 Cindi Z 2021-02-17 J Acquir Immune Defic Syndr www.ncbi.nlm.nih.gov/pubmed/33625064 Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens. Response to tenofovir alafenamide (body weight gain) 160 Black South African individuals NA Illumina [NR] (imputed) 2 response to tenofovir, body weight gain http://www.ebi.ac.uk/efo/EFO_0009279, http://www.ebi.ac.uk/efo/EFO_0004566 GCST011959 Genome-wide genotyping array 2021-06-23 33625064 Cindi Z 2021-02-17 J Acquir Immune Defic Syndr www.ncbi.nlm.nih.gov/pubmed/33625064 Genetic Associations with Weight Gain among South Africans who Initiated Dolutegravir- and Tenofovir-containing Regimens. Response to tenofovir disoproxil fumarate (body weight gain) 154 Black South African individuals NA Illumina [NR] (imputed) 1 response to tenofovir, body weight gain http://www.ebi.ac.uk/efo/EFO_0009279, http://www.ebi.ac.uk/efo/EFO_0004566 GCST011958 Genome-wide genotyping array 2018-10-17 30073298 Schellevis RL 2018-08-02 JAMA Ophthalmol www.ncbi.nlm.nih.gov/pubmed/30073298 Role of the Complement System in Chronic Central Serous Chorioretinopathy: A Genome-Wide Association Study. Chronic central serous retinopathy 521 European ancestry cases, 3,577 European ancestry controls Illumina [11526719] (imputed) 7 chronic central serous retinopathy http://www.ebi.ac.uk/efo/EFO_0009363 GCST006416 Genome-wide genotyping array 2018-10-16 30071075 Jiang L 2018-08-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/30071075 A genome-wide association study of energy intake and expenditure. Energy expenditure 5,461 European ancestry lean females, 2,726 European ancestry lean males, 6,563 European ancestry overweight or obese females, 4,020 European ancestry overweight or obese males. NA Affymetrix, Illumina [NR] (imputed) 11 energy expenditure measurement http://www.ebi.ac.uk/efo/EFO_0008005 GCST006403 Genome-wide genotyping array 2018-10-16 30071075 Jiang L 2018-08-02 PLoS One www.ncbi.nlm.nih.gov/pubmed/30071075 A genome-wide association study of energy intake and expenditure. Energy intake 5,461 European ancestry lean females, 2,726 European ancestry lean males, 6,563 European ancestry overweight or obese females, 4,020 European ancestry overweight or obese males. NA Affymetrix, Illumina [NR] (imputed) 4 energy intake measurement http://www.ebi.ac.uk/efo/EFO_0009374 GCST006402 Genome-wide genotyping array 2019-08-01 30092369 Mainali B 2018-08-06 Papillomavirus Res www.ncbi.nlm.nih.gov/pubmed/30092369 Variants in Immune-related Genes and Genital HPV 16 Persistence in Men. Infection persistence (>18 months) in genital human papillomavirus 16 infection 21 European ancestry male cases, 15 Brazilian ancestry male cases, 4 African-American male cases, 62 European ancestry male controls, 69 Brazilian ancestry male controls, 20 African-American male controls NA Affymetrix [605885] 2 chronic human papillomavirus infection http://www.ebi.ac.uk/efo/EFO_0010060 GCST008308 Genome-wide genotyping array 2021-04-16 32981348 Klarin D 2020-09-28 Circulation www.ncbi.nlm.nih.gov/pubmed/32981348 Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Abdominal aortic aneurysm 7,642 European ancestry cases, 172,172 European ancestry controls 2,835 European ancestry cases, 107,469 European ancestry controls Affymetrix [18689289] (imputed) 4 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST011495 Genome-wide genotyping array 2021-04-16 32981348 Klarin D 2020-09-28 Circulation www.ncbi.nlm.nih.gov/pubmed/32981348 Genetic Architecture of Abdominal Aortic Aneurysm in the Million Veteran Program. Abdominal aortic aneurysm 7,642 European ancestry cases, 172,172 European ancestry controls 4,972 European ancestry cases, 99,858 European ancestry controls Affymetrix [18689289] (imputed) 10 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST011496 Genome-wide genotyping array 2019-08-07 28686080 Liu N 2017-07-07 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/28686080 Influence of common and rare genetic variation on warfarin dose among African-Americans and European-Americans using the exome array. Warfarin maintenance dose (adjusted for clinical factors) 701 European ancestry individuals, 539 African American individuals 137 European Ancestry individuals, 330 African American individuals Illumina [247870] 3 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST008374 Exome genotyping array [Exome array] 2021-08-16 33633301 Wang M 2021-02-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33633301 A genome-wide association and polygenic risk score study on abnormal electrocardiogram in a Chinese population. Abnormal ECG 324 Chinese ancestry cases, 682 Chinese ancestry controls Chinese ancestry cases, Chinese ancestry controls Affymetrix [243487] 0 Abnormal EKG http://purl.obolibrary.org/obo/HP_0003115 GCST012208 Genome-wide genotyping array 2021-10-04 33610756 Gao H 2021-02-18 Mitochondrion www.ncbi.nlm.nih.gov/pubmed/33610756 A Genome-Wide Association Study in Human Lymphoblastoid Cells Supports Safety of Mitochondrial Complex I Inhibitor. tricyclic pyrone compound response (IC50) 36 African American lymphoblastoid cell lines, 84 European ancestry lymphoblastoid cell lines, 76 Han Chinese ancestry lymphoblastoid cell lines NA Affymetrix, Illumina [1184972] 13 response to mitochondrial complex I inhibitor http://www.ebi.ac.uk/efo/EFO_0600033 GCST012420 Genome-wide genotyping array 2018-11-05 30160337 Asleh R 2018-08-30 Clin Transplant www.ncbi.nlm.nih.gov/pubmed/30160337 Genome Wide Association Study Reveals Novel Genetic Loci Associated With Change in Renal Function in Heart Transplant Recipients. Glomerular filtration rate change in heart transplantation 243 European ancestry individuals, 1 American Indian ancestry individual, 7 individuals NA Illumina [314903] (imputed) 5 response to transplant, GFR change measurement http://www.ebi.ac.uk/efo/EFO_0007043, http://www.ebi.ac.uk/efo/EFO_0006829 GCST006496 Genome-wide genotyping array 2021-03-15 33491046 Torres GG 2021-01-25 J Gerontol A Biol Sci Med Sci www.ncbi.nlm.nih.gov/pubmed/33491046 Exome-wide association study identifies FN3KRP and PGP as new candidate longevity genes. Longevity 1,248 European ancestry cases, 6,941 European ancestry controls 2,266 European ancestry cases, 2,568 European ancestry controls Illumina [62488] 0 longevity http://www.ebi.ac.uk/efo/EFO_0004300 GCST011276 Exome genotyping array [Exome array] 2019-02-27 30679814 van Setten J 2019-01-24 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30679814 Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. PR interval 2,370 Erasmus Rucphen Family (founder/genetic isolate) individuals, 29,325 European ancestry individuals 391 Carlantino (founder/genetic isolate) individuals, 981 Friuli Venezia Giulia (founder/genetic isolate) individuals, 31,033 European ancestry individuals, 2,070 African American individuals Affymetrix, Illumina [at least 19000000] (imputed) 15 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST007226 Genome-wide genotyping array 2019-02-27 30679814 van Setten J 2019-01-24 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30679814 Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. QRS duration 2,177 Erasmus Rucphen Family (founder/genetic isolate) individuals, 23,332 European ancestry individuals 391 Carlantino (founder/genetic isolate) individuals, 981 Friuli Venezia Giulia (founder/genetic isolate) individuals, 30,760 European ancestry individuals, 2,048 African American individuals Affymetrix, Illumina [at least 19000000] (imputed) 12 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST007227 Genome-wide genotyping array 2019-02-26 30679814 van Setten J 2019-01-24 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30679814 Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. QT interval 2,332 Erasmus Rucphen Family (founder/genetic isolate) individuals, 24,462 European ancestry individuals 391 Carlantino (founder/genetic isolate) individuals, 981 Friuli Venezia Giulia (founder/genetic isolate) individuals, 31,225 European ancestry individuals, 2,048 African American individuals Affymetrix, Illumina [at least 19000000] (imputed) 13 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST007218 Genome-wide genotyping array 2019-02-26 30679814 van Setten J 2019-01-24 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/30679814 Genome-wide association meta-analysis of 30,000 samples identifies seven novel loci for quantitative ECG traits. RR interval (heart rate) 2,006 Erasmus Rucphen Family (founder/genetic isolate) individuals, 26,692 European ancestry individuals NA Affymetrix, Illumina [at least 19000000] (imputed) 8 RR interval http://www.ebi.ac.uk/efo/EFO_0004831 GCST007217 Genome-wide genotyping array 2019-02-06 30643196 Hitomi Y 2019-01-14 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30643196 POGLUT1, the putative effector gene driven by rs2293370 in primary biliary cholangitis susceptibility locus chromosome 3q13.33. Primary biliary cholangitis 1,855 Japanese ancestry cases, 1,719 Japanese ancestry controls NA Affymetrix [NR] (imputed) 5 primary biliary cirrhosis http://www.ebi.ac.uk/efo/EFO_1001486 GCST007036 Genome-wide genotyping array 2019-05-10 30957308 Blauwendraat C 2019-04-07 Mov Disord www.ncbi.nlm.nih.gov/pubmed/30957308 Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms. Parkinson's disease (age of onset) 17,996 cases 10,572 cases Illumina [6850647] (imputed) 4 age of onset of Parkinson disease http://purl.obolibrary.org/obo/OBA_2001009 GCST007780 Genome-wide genotyping array 2019-04-18 30779856 Lu HF 2019-02-19 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30779856 A meta-analysis of genome-wide association studies identifies three loci associated with stiffness index of the calcaneus. Calcaneus stiffness index 7,742 Taiwanese ancestry individuals 2,955 Korean ancestry individuals Affymetrix [~ 6100000] (imputed) 3 calcaneal bone quantitative ultrasound measurement http://www.ebi.ac.uk/efo/EFO_0007772 GCST007616 Genome-wide genotyping array 2019-04-17 30636644 Nazarian A 2019-01-12 Alzheimers Res Ther www.ncbi.nlm.nih.gov/pubmed/30636644 Genome-wide analysis of genetic predisposition to Alzheimer's disease and related sex disparities. Alzheimer's disease 952 European ancestry male cases, 1,789 European ancestry female cases, 6,337 European ancestry male controls, 8,402 European ancestry female controls NA Affymetrix, Illumina [2928658] (imputed) 91 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST007600 Genome-wide genotyping array 2019-05-13 30952644 El Charif O 2019-04-05 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/30952644 Clinical and Genome-Wide Analysis of Cisplatin-Induced Tinnitus Implicates Novel Ototoxic Mechanisms. Tinnitus in cisplatin-treated testicular cancer 154 European ancestry cases, 608 European ancestry controls NA Illumina [7225561] (imputed) 10 Tinnitus, response to cisplatin http://purl.obolibrary.org/obo/HP_0000360, http://purl.obolibrary.org/obo/GO_0072718 GCST007796 Genome-wide genotyping array 2019-05-15 30944420 Liu L 2019-04-03 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/30944420 Identification of a 1p21 independent functional variant for abdominal obesity. Trunk fat mass adjusted for trunk lean mass 8,736 European ancestry individuals, 1,541 East Asian ancestry individuals, 445 Hispanic ancestry individuals, 847 African-American ancestry individuals NA Affymetrix, Illumina [12061510] (imputed) 5 lean mass-adjusted fat body mass http://www.ebi.ac.uk/efo/EFO_0009890 GCST007816 Genome-wide genotyping array 2019-09-10 30945665 Bandesh K 2019-03-01 J Genet www.ncbi.nlm.nih.gov/pubmed/30945665 Genomewide association study of C-peptide surfaces key regulatory genes in Indians. C-peptide levels 877 Indo-European ancestry individuals 1,829 Indo-European ancestry individuals, 773 Hispanic individuals Illumina [552011] 1 C-peptide measurement http://www.ebi.ac.uk/efo/EFO_0005187 GCST008641 Genome-wide genotyping array 2019-07-29 30940813 Kranzler HR 2019-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30940813 Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. Alcohol use disorder (consumption score) 200,680 European American individuals, 56,495 African American individuals, 14,112 Latino American individuals, 1,366 East Asian American individuals, 189 South Asian American individuals NA Affymetrix [up to 12500000] (imputed) 32 alcohol use disorder measurement, longitudinal alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0009458, http://www.ebi.ac.uk/efo/EFO_0007645 GCST008258 Genome-wide genotyping array 2019-07-29 30940813 Kranzler HR 2019-04-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30940813 Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. Alcohol use disorder 34,658 European American cases, 167,346 European American controls, 17,267 African American cases, 39,381 African American controls, 3,449 Latino American cases, 10,726 Latino American controls, 164 East Asian American cases, 1,210 East Asian American controls, 46 South Asian American cases, 144 South Asian American controls NA Affymetrix [up to 12500000] (imputed) 25 alcohol use disorder measurement, alcohol dependence http://www.ebi.ac.uk/efo/EFO_0009458, http://purl.obolibrary.org/obo/MONDO_0007079 GCST008259 Genome-wide genotyping array 2021-08-04 33613413 Park KW 2021-02-04 Front Neurol www.ncbi.nlm.nih.gov/pubmed/33613413 Genomic Association Study for Cognitive Impairment in Parkinson's Disease. cognitive impairment (MMSE score) in Parkinson’s disease 347 Korean ancestry MMSE score <26 individuals, 682 Korean ancestry MMSE score >=26 individuals NA NR [563715] 1 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST012162 Genome-wide genotyping array 2021-08-04 33613413 Park KW 2021-02-04 Front Neurol www.ncbi.nlm.nih.gov/pubmed/33613413 Genomic Association Study for Cognitive Impairment in Parkinson's Disease. cognitive impairment (MoCA score) in Parkinson’s disease 222 Korean ancestry MoCA score <24 individuals, 272 Korean ancestry MoCA score >=24 individuals NA NR [523758] 1 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST012161 Genome-wide genotyping array 2018-11-01 30152087 Ostrom QT 2018-08-27 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/30152087 Age-specific genome-wide association study in glioblastoma identifies increased proportion of 'lower grade glioma'-like features associated with younger age. Glioblastoma (age-stratified) 1,533 cases diagnosed below median age, 1,476 cases diagnosed at median age, 1,503 cases diagnosed above median age, 10,582 controls, NA NR [NR] (imputed) 20 age at onset, glioblastoma multiforme http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0000519 GCST006480 Genome-wide genotyping array 2020-04-27 30659077 Onengut-Gumuscu S 2019-01-18 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/30659077 Type 1 Diabetes Risk in African-Ancestry Participants and Utility of an Ancestry-Specific Genetic Risk Score. Type 1 diabetes 1,021 African American cases, 2,928 African American controls NA Illumina [114874] 6 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST009916 Targeted genotyping array [ImmunoChip] 2019-04-25 30888730 Hsu YH 2019-03-19 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30888730 Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry. Femoral neck length 18,719 individuals 8,334 individuals Affymetrix, Illumina [up to 2622085] (imputed) 2 femoral neck bone geometry http://www.ebi.ac.uk/efo/EFO_0004511 GCST007639 Genome-wide genotyping array 2019-04-25 30888730 Hsu YH 2019-03-19 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30888730 Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry. Narrowest width of the femoral neck 18,719 individuals 8,334 individuals Affymetrix, Illumina [up to 2622085] (imputed) 2 femoral neck bone geometry http://www.ebi.ac.uk/efo/EFO_0004511 GCST007640 Genome-wide genotyping array 2019-04-25 30888730 Hsu YH 2019-03-19 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30888730 Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry. Femoral neck section modulus 18,719 individuals 8,334 individuals Affymetrix, Illumina [up to 2622085] (imputed) 1 femoral neck bone geometry http://www.ebi.ac.uk/efo/EFO_0004511 GCST007641 Genome-wide genotyping array 2019-04-25 30888730 Hsu YH 2019-03-19 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/30888730 Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry. Femoral neck-shaft angle 18,719 individuals 8,334 individuals Affymetrix, Illumina [up to 2622085] (imputed) 0 femoral neck bone geometry http://www.ebi.ac.uk/efo/EFO_0004511 GCST007642 Genome-wide genotyping array 2018-11-07 30169916 Sun Y 2018-08-31 J Eur Acad Dermatol Venereol www.ncbi.nlm.nih.gov/pubmed/30169916 Investigation of the Predisposing Factor of Pemphigus and its clinical subtype through a Genome-wide association and next generation sequence analysis. Pemphigus vulgaris 101 Chinese ancestry cases, 844 Chinese ancestry controls at least 56 Chinese ancestry cases, up to 996 Chinese ancestry controls Illumina [5546030] (imputed) 4 pemphigus vulgaris http://www.ebi.ac.uk/efo/EFO_0004719 GCST006521 Genome-wide genotyping array 2018-11-07 30169916 Sun Y 2018-08-31 J Eur Acad Dermatol Venereol www.ncbi.nlm.nih.gov/pubmed/30169916 Investigation of the Predisposing Factor of Pemphigus and its clinical subtype through a Genome-wide association and next generation sequence analysis. Pemphigus foliaceus 65 Chinese ancestry cases, 844 Chinese ancestry controls at least 49 Chinese ancestry cases, up to 996 Chinese ancestry controls Illumina [5546030] (imputed) 2 pemphigus foliaceus http://www.ebi.ac.uk/efo/EFO_0008601 GCST006520 Genome-wide genotyping array 2019-02-13 30111768 Yao C 2018-08-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30111768 Genome-wide mapping of plasma protein QTLs identifies putatively causal genes and pathways for cardiovascular disease. Blood protein levels 6861 European ancestry individuals 4298 European ancestry individuals Affymetrix, Illumina [8509364] (imputed) 8 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST007128 Genome-wide genotyping array 2019-05-07 30898391 Lawrenson K 2019-03-19 Gynecol Oncol www.ncbi.nlm.nih.gov/pubmed/30898391 Genome-wide association studies identify susceptibility loci for epithelial ovarian cancer in east Asian women. Epithelial ovarian cancer 3,238 East Asian ancestry cases, 4,083 East Asian ancestry controls NA Illumina [11595112] (imputed) 126 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST007728 Genome-wide genotyping array 2021-08-10 33627384 Matejcic M 2021-02-24 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/33627384 Rare variants in the DNA repair pathway and the risk of colorectal cancer. Colorectal cancer 2,327 European ancestry cases, 2,966 European ancestry controls NA Illumina [142390] 2 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST012176 Genome-wide genotyping array 2019-05-21 30891314 Saad MN 2019-01-18 J Adv Res www.ncbi.nlm.nih.gov/pubmed/30891314 Studying the effects of haplotype partitioning methods on the RA-associated genomic results from the North American Rheumatoid Arthritis Consortium (NARAC) dataset. Rheumatoid arthritis 868 European ancestry cases, 1,194 European ancestry controls NA NR [509413] 31 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST007843 Genome-wide genotyping array 2019-04-30 30886212 Eszlari N 2019-03-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30886212 Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination. Rumination (response to stress) 1,758 European ancestry individuals NA Illumina [3474641] (imputed) 3 ruminative stress response http://www.ebi.ac.uk/efo/EFO_0009857 GCST007677 Genome-wide genotyping array 2019-04-30 30886212 Eszlari N 2019-03-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30886212 Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination. Brooding (response to stress) 1,758 European ancestry individuals NA Illumina [3474641] (imputed) 3 brooding stress response http://www.ebi.ac.uk/efo/EFO_0009858 GCST007678 Genome-wide genotyping array 2019-04-30 30886212 Eszlari N 2019-03-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30886212 Genome-wide association analysis reveals KCTD12 and miR-383-binding genes in the background of rumination. Reflection (response to stress) 1,758 European ancestry individuals NA Illumina [3474641] (imputed) 4 reflective stress response http://www.ebi.ac.uk/efo/EFO_0009859 GCST007679 Genome-wide genotyping array 2019-05-02 30867560 Hill WD 2019-03-13 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30867560 Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life. Worry/vulnerability (special factor of neuroticism) 270,059 British ancestry individuals NA Affymetrix [18485882] (imputed) 14 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST007708 Genome-wide genotyping array 2019-05-02 30867560 Hill WD 2019-03-13 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30867560 Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life. Anxiety/tension (special factor of neuroticism) 270,059 British ancestry individuals NA Affymetrix [18485882] (imputed) 20 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST007710 Genome-wide genotyping array 2019-05-02 30867560 Hill WD 2019-03-13 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30867560 Genetic contributions to two special factors of neuroticism are associated with affluence, higher intelligence, better health, and longer life. General factor of neuroticism 270,059 British ancestry individuals NA Affymetrix [18485882] (imputed) 308 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST007709 Genome-wide genotyping array 2019-01-21 30134812 Chattopadhyay S 2018-06-11 Mol Med www.ncbi.nlm.nih.gov/pubmed/30134812 Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study. Monoclonal gammopathy of undetermined significance 243 German ancestry cases, 1,285 German ancestry controls NA Illumina [489555] 15 monoclonal gammopathy http://www.ebi.ac.uk/efo/EFO_0000203 GCST006917 Genome-wide genotyping array 2021-03-07 32424139 Alemany-Navarro M 2020-05-18 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/32424139 Looking into the genetic bases of OCD dimensions: a pilot genome-wide association study. Sexual/religious dimension in obsessive compulsive disorder 95 European ancestry cases, 280 European ancestry controls NA Illumina [258937] 0 obsessive-compulsive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007802 GCST011236 Targeted genotyping array [PsychArray] 2019-02-07 30046033 van Setten J 2018-07-25 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30046033 PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity. PR interval 92,340 European ancestry individuals NA Affymetrix, Illumina [2712613] (imputed) 44 PR interval http://www.ebi.ac.uk/efo/EFO_0004462 GCST007045 Genome-wide genotyping array 2018-08-23 29703947 Jawinski P 2018-04-27 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29703947 Human brain arousal in the resting state: a genome-wide association study. Resting-state electroencephalogram vigilance 1,877 European ancestry individuals NA Affymetrix [8042262] (imputed) 45 electroencephalogram measurement http://www.ebi.ac.uk/efo/EFO_0004357 GCST006138 Genome-wide genotyping array 2021-03-22 33482370 Kim SK 2021-01-19 J Shoulder Elbow Surg www.ncbi.nlm.nih.gov/pubmed/33482370 A Genome Wide Association Study For Shoulder Impingement and Rotator Cuff Disease. Shoulder impingement or rotator cuff tear 3,864 European ancestry shoulder impingement cases, 5,701 European ancestry rotator cuff tear cases, up to 614,568 European ancestry controls NA Affymetrix [up to 17556449] (imputed) 9 rotator cuff tear, shoulder impingement syndrome http://www.ebi.ac.uk/efo/EFO_1001250, http://www.ebi.ac.uk/efo/EFO_1001178 GCST011377 Genome-wide genotyping array 2021-03-22 33482370 Kim SK 2021-01-19 J Shoulder Elbow Surg www.ncbi.nlm.nih.gov/pubmed/33482370 A Genome Wide Association Study For Shoulder Impingement and Rotator Cuff Disease. Shoulder impingement 3,864 European ancestry cases, 208,258 European ancestry controls NA Affymetrix [17556449] (imputed) 4 shoulder impingement syndrome http://www.ebi.ac.uk/efo/EFO_1001178 GCST90014054 Genome-wide genotyping array 2019-04-25 30889042 Innocenti F 2019-03-18 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/30889042 An initial genetic analysis of gemcitabine-induced high-grade neutropenia in pancreatic cancer patients CALGB 80303 (Alliance). Gemcitabine-induced early high-grade neutropenia in pancreatic cancer 294 European ancestry cases NA Illumina [457310] 6 neutropenia, response to gemcitabine http://purl.obolibrary.org/obo/MONDO_0001475, http://purl.obolibrary.org/obo/GO_0036272 GCST007643 Genome-wide genotyping array 2021-08-17 33635380 Kouri N 2021-02-26 Acta Neuropathol www.ncbi.nlm.nih.gov/pubmed/33635380 Latent trait modeling of tau neuropathology in progressive supranuclear palsy. Progressive supranuclear palsy 481 individuals 401 individuals Illumina [NR] (imputed) 6 progressive supranuclear palsy http://purl.obolibrary.org/obo/MONDO_0019037 GCST012209 Genome-wide genotyping array 2018-09-19 30067105 Chang LC 2018-08-01 Expert Opin Drug Saf www.ncbi.nlm.nih.gov/pubmed/30067105 Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions. Adverse response to antithyroid drugs in Graves disease 24 East Asian ancestry cases, 423 East Asian ancestry controls 45 East Asian ancestry cases, 137 East Asian ancestry controls Affymetrix [574162] 2 response to anti-thyroid drug http://www.ebi.ac.uk/efo/EFO_0007838 GCST006278 Genome-wide genotyping array 2019-01-07 30060048 Wang SC 2018-07-27 Int J Neuropsychopharmacol www.ncbi.nlm.nih.gov/pubmed/30060048 GRK5 is associated with the regulation of methadone dosage in heroin dependence. Methadone dose in opioid dependence 344 Taiwanese ancestry cases NA Affymetrix [615216] 2 methadone dose measurement http://www.ebi.ac.uk/efo/EFO_0007907 GCST006856 Genome-wide genotyping array 2019-01-22 30065583 Choi MR 2018-06-28 Ann Dermatol www.ncbi.nlm.nih.gov/pubmed/30065583 Possible Role of Single Stranded DNA Binding Protein 3 on Skin Hydration by Regulating Epidermal Differentiation. Skin hydration 100 Korean ancestry individuals NA Affymetrix [501262] 0 skin hydration measurement http://www.ebi.ac.uk/efo/EFO_0009586 GCST006939 Genome-wide genotyping array 2019-04-29 30648747 Dudenkov TM 2019-01-16 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/30648747 Anastrozole Aromatase Inhibitor Plasma Drug Concentration Genome-Wide Association Study: Functional Epistatic Interaction between SLC38A7 and ALPPL2. Plasma anastrozole concentration in anastrozole-treated estrogen receptor positive breast cancer 634 European ancestry individuals, 40 African ancestry individuals, 13 Asian ancestry individuals NA Illumina [~ 600000] (imputed) 47 response to aromatase inhibitor http://purl.obolibrary.org/obo/GO_0061477 GCST007664 Genome-wide genotyping array 2019-04-09 30794219 MacInnes SJ 2019-02-01 Clin Orthop Relat Res www.ncbi.nlm.nih.gov/pubmed/30794219 The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? Osteolysis in total hip arthroplasty 1,096 European ancestry cases, 2,418 European ancestry controls NA Illumina [5411522] (imputed) 5 periprosthetic osteolysis http://www.ebi.ac.uk/efo/EFO_0009761 GCST007549 Genome-wide genotyping array 2019-04-09 30794219 MacInnes SJ 2019-02-01 Clin Orthop Relat Res www.ncbi.nlm.nih.gov/pubmed/30794219 The 2018 Otto Aufranc Award: How Does Genome-wide Variation Affect Osteolysis Risk After THA? Osteolysis in total hip arthroplasty (time to prosthesis revision) 1,096 European ancestry cases NA Illumina [5418572] (imputed) 11 periprosthetic osteolysis, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0009761, http://www.ebi.ac.uk/efo/EFO_0008336 GCST007550 Genome-wide genotyping array 2019-07-11 30654714 Hurst Z 2019-01-18 Thyroid www.ncbi.nlm.nih.gov/pubmed/30654714 Risk Haplotypes Uniquely Associated with Radioiodine Refractory Thyroid Cancer Patients of High African Ancestry. Radioiodine-refractory disease in thyroid cancer 244 European ancestry cases, 901 European ancestry controls, 9 African American cases, 46 African American controls NA Illumina [NR] (imputed) 0 response to radioiodine http://www.ebi.ac.uk/efo/EFO_0009962 GCST008107 Genome-wide genotyping array 2019-05-07 30945699 Wei J 2019-04-04 Med Sci Monit www.ncbi.nlm.nih.gov/pubmed/30945699 Genome-Wide Association Study Identifies a Genetic Prediction Model for Postoperative Survival in Patients with Hepatocellular Carcinoma. Postoperative survival time in hepatocellular carcinoma 367 East Asian ancestry cases 758 East Asian ancestry cases Affymetrix [630573] 5 overall survival http://www.ebi.ac.uk/efo/EFO_0000638 GCST007731 Genome-wide genotyping array 2019-05-03 30941828 Bi X 2019-04-03 Genet Epidemiol www.ncbi.nlm.nih.gov/pubmed/30941828 Common genetic variants have associations with human cortical brain regions and risk of schizophrenia. Cortical brain region measurements (area, volume and thickness) 901 children and adolescents 812 children and adolescents Affymetrix, Illumina [260781] 2 brain measurement http://www.ebi.ac.uk/efo/EFO_0004464 GCST007712 Genome-wide genotyping array 2019-04-30 30796134 Soderholm M 2019-02-22 Neurology www.ncbi.nlm.nih.gov/pubmed/30796134 Genome-wide association meta-analysis of functional outcome after ischemic stroke. 3-month functional outcome in ischaemic stroke (modified Rankin score) 1,832 European and unknown ancestry modified Rankin score 0-1 cases, 2,620 European and unknown ancestry modified Rankin score 2-6 cases NA Affymetrix, Illumina [~ 8500000] (imputed) 17 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST007672 Genome-wide genotyping array 2019-04-30 30796134 Soderholm M 2019-02-22 Neurology www.ncbi.nlm.nih.gov/pubmed/30796134 Genome-wide association meta-analysis of functional outcome after ischemic stroke. 3-month functional outcome in ischaemic stroke (modified Rankin score) 6,165 European and unknown ancestry individuals NA Affymetrix, Illumina [~ 8500000] (imputed) 19 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST007673 Genome-wide genotyping array 2019-04-30 30796134 Soderholm M 2019-02-22 Neurology www.ncbi.nlm.nih.gov/pubmed/30796134 Genome-wide association meta-analysis of functional outcome after ischemic stroke. 3-month functional outcome in lacunar ischaemic stroke (modified Rankin score) 992 European and unknown ancestry individuals NA Affymetrix, Illumina [~ 8500000] (imputed) 2 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST007674 Genome-wide genotyping array 2019-04-30 30796134 Soderholm M 2019-02-22 Neurology www.ncbi.nlm.nih.gov/pubmed/30796134 Genome-wide association meta-analysis of functional outcome after ischemic stroke. 3-month functional outcome in non-lacunar ischaemic stroke (modified Rankin score) 3,991 European and unknown ancestry individuals NA Affymetrix, Illumina [~ 8500000] (imputed) 5 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST007675 Genome-wide genotyping array 2019-04-30 30796134 Soderholm M 2019-02-22 Neurology www.ncbi.nlm.nih.gov/pubmed/30796134 Genome-wide association meta-analysis of functional outcome after ischemic stroke. 3-month functional outcome in ischaemic stroke (modified Rankin score) 3,830 European and unknown ancestry modified Rankin score 0-2 cases, 2,335 European and unknown ancestry modified Rankin score 3-6 cases NA Affymetrix, Illumina [~ 8500000] (imputed) 18 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST007676 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Sleep duration 85,449 European ancestry individuals 5,819 European ancestry individuals Affymetrix [11977111] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST007801 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Sleep duration (variability) 84,441 European ancestry individuals 5,819 European ancestry individuals Affymetrix [11977111] (imputed) 0 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST007802 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Sleep efficiency 84,810 European ancestry individuals 5,819 European ancestry individuals Affymetrix [11977111] (imputed) 0 sleep quality http://www.ebi.ac.uk/efo/EFO_0005272 GCST007803 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Sleep (number of episodes) 84,810 European ancestry individuals 4,401 European ancestry individuals Affymetrix [11977111] (imputed) 1 sleep quality http://www.ebi.ac.uk/efo/EFO_0005272 GCST007804 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Sleep (time to least active 5 hours) 85,205 European ancestry individuals 5,819 European ancestry individuals Affymetrix [11977111] (imputed) 0 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST007805 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Time to most active 10 hours 85,670 European ancestry individuals 5,819 European ancestry individuals Affymetrix [11977111] (imputed) 0 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST007806 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Sleep (time to midpoint) 84,810 European ancestry individuals 5,819 European ancestry individuals Affymetrix [11977111] (imputed) 0 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST007807 Genome-wide genotyping array 2019-05-15 30952852 Jones SE 2019-04-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30952852 Genetic studies of accelerometer-based sleep measures yield new insights into human sleep behaviour. Diurnal inactivity 84,757 European ancestry individuals 4,401 European ancestry individuals Affymetrix [11977111] (imputed) 0 daytime rest measurement http://www.ebi.ac.uk/efo/EFO_0007828 GCST007808 Genome-wide genotyping array 2019-02-11 30228239 Wojcik GL 2018-09-18 MBio www.ncbi.nlm.nih.gov/pubmed/30228239 Genome-Wide Association Study Reveals Genetic Link between Diarrhea-Associated Entamoeba histolytica Infection and Inflammatory Bowel Disease. Diarrhoea-associated Entamoeba histolytica infection 170 Bangladeshi ancestry cases, 574 Bangladeshi ancestry controls NA Illumina [6703908] (imputed) 1 amebiasis http://www.ebi.ac.uk/efo/EFO_0007144 GCST007109 Genome-wide genotyping array 2019-04-18 30940143 Zhu Z 2019-04-02 Respir Res www.ncbi.nlm.nih.gov/pubmed/30940143 Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. Resting heart rate 458,969 European ancestry individuals NA Affymetrix [5264922] (imputed) 0 resting heart rate http://www.ebi.ac.uk/efo/EFO_0004351 GCST007609 Genome-wide genotyping array 2019-04-18 30940143 Zhu Z 2019-04-02 Respir Res www.ncbi.nlm.nih.gov/pubmed/30940143 Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. Hypertension 144,793 European ancestry cases, 313,761 European ancestry controls NA Affymetrix [5265189] (imputed) 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST007610 Genome-wide genotyping array 2019-04-18 30940143 Zhu Z 2019-04-02 Respir Res www.ncbi.nlm.nih.gov/pubmed/30940143 Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. Chronic obstructive pulmonary disease or high blood pressure (pleiotropy) 12,550 European and unknown ancestry chronic obstructive pulmonary disease cases, 46,368 European and unknown ancestry controls, 144,793 European ancestry high blood pressure cases, 313,761 European ancestry controls NA Affymetrix [up to 7325140] (imputed) 22 hypertension, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0000341 GCST007611 Genome-wide genotyping array 2019-04-18 30940143 Zhu Z 2019-04-02 Respir Res www.ncbi.nlm.nih.gov/pubmed/30940143 Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. Chronic obstructive pulmonary disease or coronary artery disease (pleiotropy) 12,550 European and unknown ancestry chronic pulmonary obstructive disease cases, 60,801 European and unknown ancestry coronary artery disease cases, 169,872 European and unknown ancestry controls NA NR [up to 8619474] (imputed) 3 chronic obstructive pulmonary disease, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0000341, http://www.ebi.ac.uk/efo/EFO_0001645 GCST007612 Genome-wide genotyping array 2019-04-18 30940143 Zhu Z 2019-04-02 Respir Res www.ncbi.nlm.nih.gov/pubmed/30940143 Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. Chronic obstructive pulmonary disease or stroke (pleiotropy) 12,550 European and unknown ancestry chronic obstructive pulmonary disease cases, 46,368 European and unknown ancestry controls, 40,585 European ancestry stroke cases, 406,111 European ancestry controls NA NR [up to 8255860] (imputed) 0 stroke, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000712, http://www.ebi.ac.uk/efo/EFO_0000341 GCST007613 Genome-wide genotyping array 2019-04-29 30940143 Zhu Z 2019-04-02 Respir Res www.ncbi.nlm.nih.gov/pubmed/30940143 Genetic overlap of chronic obstructive pulmonary disease and cardiovascular disease-related traits: a large-scale genome-wide cross-trait analysis. Chronic obstructive pulmonary disease or resting heart rate (pleiotropy) 12,550 European and unknown ancestry chronic obstructive pulmonary disease cases, 46,368 European and unknown ancestry controls, 458,969 European ancestry individuals NA Affymetrix [up to 7325140] (imputed) 21 resting heart rate, chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0004351, http://www.ebi.ac.uk/efo/EFO_0000341 GCST007656 Genome-wide genotyping array 2019-08-21 30942860 Shin J 2019-04-03 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/30942860 Novel genetic locus of visceral fat and systemic inflammation. Visceral fat 1589 French-Canadian ancestry individuals NA Illumina [8511049] (imputed) 52 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST008473 Genome-wide genotyping array 2019-03-28 30787463 Escala-Garcia M 2019-02-21 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/30787463 Genome-wide association study of germline variants and breast cancer-specific mortality. Breast cancer specific mortality in breast cancer 7,697 European ancestry cases, 88,964 European ancestry controls NA Affymetrix, Illumina [~ 10400000] (imputed) 47 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST007477 Genome-wide genotyping array 2019-03-28 30787463 Escala-Garcia M 2019-02-21 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/30787463 Genome-wide association study of germline variants and breast cancer-specific mortality. Breast cancer specific mortality in estrogen receptor negative breast cancer 2,125 European ancestry cases, 14,047 European ancestry controls NA Affymetrix, Illumina [~ 10400000] (imputed) 28 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST007476 Genome-wide genotyping array 2019-03-28 30787463 Escala-Garcia M 2019-02-21 Br J Cancer www.ncbi.nlm.nih.gov/pubmed/30787463 Genome-wide association study of germline variants and breast cancer-specific mortality. Breast cancer specific mortality in estrogen receptor positive breast cancer 4,116 European ancestry cases, 60,055 European ancestry controls NA Affymetrix, Illumina [~ 10400000] (imputed) 22 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST007475 Genome-wide genotyping array 2019-05-15 30946739 Hu B 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946739 Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Facial attractiveness (female raters) 3,928 European ancestry individuals 455 European ancestry individuals Illumina [7251583] (imputed) 1 facial attractiveness measurement http://www.ebi.ac.uk/efo/EFO_0009892 GCST007818 Genome-wide genotyping array 2019-05-15 30946739 Hu B 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946739 Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Facial attractiveness (male raters) 3,928 European ancestry individuals NA Illumina [7251583] (imputed) 2 facial attractiveness measurement http://www.ebi.ac.uk/efo/EFO_0009892 GCST007817 Genome-wide genotyping array 2019-05-15 30946739 Hu B 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946739 Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Facial attractiveness (male raters) 1,792 European ancestry male individuals NA Illumina [7251583] (imputed) 1 facial attractiveness measurement http://www.ebi.ac.uk/efo/EFO_0009892 GCST007823 Genome-wide genotyping array 2019-05-15 30946739 Hu B 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946739 Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Facial attractiveness (male raters) 2,062 European ancestry female individuals 213 European ancestry female individuals Illumina [7251583] (imputed) 1 facial attractiveness measurement http://www.ebi.ac.uk/efo/EFO_0009892 GCST007822 Genome-wide genotyping array 2019-05-15 30946739 Hu B 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946739 Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Facial attractiveness (female raters) 1,792 European ancestry male individuals NA Illumina [7251583] (imputed) 3 facial attractiveness measurement http://www.ebi.ac.uk/efo/EFO_0009892 GCST007821 Genome-wide genotyping array 2019-05-15 30946739 Hu B 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946739 Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Facial attractiveness (female raters) 2,062 European ancestry female individuals NA Illumina [7251583] (imputed) 2 facial attractiveness measurement http://www.ebi.ac.uk/efo/EFO_0009892 GCST007820 Genome-wide genotyping array 2019-05-15 30946739 Hu B 2019-04-04 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/30946739 Genome-wide association study reveals sex-specific genetic architecture of facial attractiveness. Facial attractiveness (male raters) 3,921 European ancestry individuals NA Illumina [156615] (imputed) 1 facial attractiveness measurement http://www.ebi.ac.uk/efo/EFO_0009892 GCST007819 Targeted genotyping array [X chromosome] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cirrhosis (Gene-based burden) 1,995 European ancestry cases, 381,355 European ancestry controls NA Illumina [185247] 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90085506 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Able to walk or cycle unaided for 10 minutes (UKB data field 6017) 77,338 European ancestry cases, 2,894 European ancestry controls NA Affymetrix, Illumina [152324] 0 ability to walk or cycle unaided for 10 minutes, self-reported http://www.ebi.ac.uk/efo/EFO_0009822 GCST90079408 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Liverfc (Gene-based burden) 2,899 European ancestry cases, 381,358 European ancestry controls NA Illumina [185267] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90085517 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm right (first instance) 79,752 European ancestry individuals NA Affymetrix, Illumina [152236] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081477 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Liverp (Gene-based burden) 6,098 European ancestry cases, 381,358 European ancestry controls NA Illumina [185341] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90085507 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm left (first instance) 78,888 European ancestry individuals NA Affymetrix, Illumina [150823] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081476 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Major bleeding (Gene-based burden) 7,582 European ancestry cases, 379,910 European ancestry controls NA Illumina [185331] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90085518 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Between one and three months (UKB data field 20438) 24,189 European ancestry cases, 54,986 European ancestry controls NA Affymetrix, Illumina [149668] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90078457 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Obesity (Gene-based burden) 104,086 European ancestry cases, 142,553 European ancestry controls NA Illumina [181622] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90085508 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Less than a month (UKB data field 20438) 11,829 European ancestry cases, 67,346 European ancestry controls NA Affymetrix, Illumina [149668] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90078456 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Overweight (Gene-based burden) 287,014 European ancestry cases, 142,553 European ancestry controls NA Illumina [185928] 0 overweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005935 GCST90085509 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - One to two years (UKB data field 20438) 8,427 European ancestry cases, 70,748 European ancestry controls NA Affymetrix, Illumina [149668] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90078460 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Possible type 2 diabetes (Gene-based burden) 2,316 European ancestry cases, 408,623 European ancestry controls NA Illumina [185701] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90085510 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Over six months but less than 12 months (UKB data field 20438) 11,994 European ancestry cases, 67,181 European ancestry controls NA Affymetrix, Illumina [149668] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90078459 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Probable type 1 diabetes (Gene-based burden) 1,290 European ancestry cases, 408,623 European ancestry controls NA Illumina [185676] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90085511 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Over three months but less than six months (UKB data field 20438) 14,051 European ancestry cases, 65,124 European ancestry controls NA Affymetrix, Illumina [149668] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90078458 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Probable type 2 diabetes (Gene-based burden) 17,719 European ancestry cases, 408,623 European ancestry controls NA Illumina [185888] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90085512 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Duration of worst depression - Over two years (UKB data field 20438) 7,396 European ancestry cases, 71,779 European ancestry controls NA Affymetrix, Illumina [149668] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90078461 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severe obesity (Gene-based burden) 7,973 European ancestry cases, 142,553 European ancestry controls NA Illumina [174212] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90085514 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression possibly related to stressful or traumatic event (UKB data field 20447) 57,607 European ancestry cases, 21,243 European ancestry controls NA Affymetrix, Illumina [149143] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078468 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severe bleeding (Gene-based burden) 39,650 European ancestry cases, 391,348 European ancestry controls NA Illumina [185951] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90085513 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Professional informed about depression (UKB data field 20448) 50,878 European ancestry cases, 27,908 European ancestry controls NA Affymetrix, Illumina [148991] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078469 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Underweight (Gene-based burden) 2,095 European ancestry cases, 140,458 European ancestry controls NA Illumina [173067] 0 underweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005936 GCST90085515 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - cease (UKB data field 20177) 73,454 European ancestry cases, 5,148 European ancestry controls NA Affymetrix, Illumina [148769] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078352 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Venous thromboembolism (Gene-based burden) 10,941 European ancestry cases, 220,601 European ancestry controls NA Illumina [180932] 0 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90085516 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble relaxing - Nearly every day (UKB data field 20515) 4,293 European ancestry cases, 134,993 European ancestry controls NA Affymetrix, Illumina [240761] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078594 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48: Spine arthritis or spondylitis (Gene-based burden) 3,855 European ancestry cases, 325,197 European ancestry controls NA Illumina [184145] 0 spondylitis http://purl.obolibrary.org/obo/MONDO_0003937 GCST90081768 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble relaxing - Several days (UKB data field 20515) 32,017 European ancestry cases, 107,269 European ancestry controls NA Affymetrix, Illumina [240761] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078592 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spontaneous pneumothorax recurrent pneumothorax (Gene-based burden) 1,058 European ancestry cases, 330,696 European ancestry controls NA Illumina [184201] 0 Spontaneous pneumothorax http://purl.obolibrary.org/obo/HP_0002108 GCST90081671 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever self harmed (UKB data field 20480) 6,056 European ancestry cases, 133,254 European ancestry controls NA Affymetrix, Illumina [240757] 0 Self-injurious behavior http://purl.obolibrary.org/obo/HP_0100716 GCST90078512 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J93: spontaneous pneumothorax recurrent pneumothorax (Gene-based burden) 839 European ancestry cases, 328,212 European ancestry controls NA Illumina [184145] 0 Spontaneous pneumothorax http://purl.obolibrary.org/obo/HP_0002108 GCST90081672 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever sought or received professional help for mental distress (UKB data field 20499) 54,821 European ancestry cases, 84,434 European ancestry controls NA Affymetrix, Illumina [240700] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90078554 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stomach disorder (Gene-based burden) 974 European ancestry cases, 330,780 European ancestry controls NA Illumina [184201] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90081673 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of depression - More than half the days (UKB data field 20510) 2,823 European ancestry cases, 136,410 European ancestry controls NA Affymetrix, Illumina [240639] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078578 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31: stomach disorder (Gene-based burden) 924 European ancestry cases, 328,128 European ancestry controls NA Illumina [184145] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90081674 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of depression - Nearly every day (UKB data field 20510) 1,965 European ancestry cases, 137,268 European ancestry controls NA Affymetrix, Illumina [240639] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078579 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stress (Gene-based burden) 977 European ancestry cases, 330,777 European ancestry controls NA Illumina [184201] 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90081945 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent feelings of depression - Several days (UKB data field 20510) 26,550 European ancestry cases, 112,683 European ancestry controls NA Affymetrix, Illumina [240639] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078577 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F43: stress (Gene-based burden) 840 European ancestry cases, 328,212 European ancestry controls NA Illumina [184145] 0 psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006783 GCST90081946 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Never true (UKB data field 20489) 1,919 European ancestry cases, 137,277 European ancestry controls NA Affymetrix, Illumina [240621] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078526 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stroke (Gene-based burden) 6,014 European ancestry cases, 325,740 European ancestry controls NA Illumina [184201] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90081649 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Often (UKB data field 20489) 35,479 European ancestry cases, 103,717 European ancestry controls NA Affymetrix, Illumina [240621] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078529 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I64: stroke (Gene-based burden) 5,459 European ancestry cases, 323,593 European ancestry controls NA Illumina [184145] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90081650 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Rarely true (UKB data field 20489) 6,336 European ancestry cases, 132,860 European ancestry controls NA Affymetrix, Illumina [240621] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078527 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Systemic lupus erythematosis (Gene-based burden) 523 European ancestry cases, 331,231 European ancestry controls NA Illumina [184201] 0 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90081796 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Sometimes true (UKB data field 20489) 22,598 European ancestry cases, 116,598 European ancestry controls NA Affymetrix, Illumina [240621] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078528 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tendonitis tendinitis tenosynovitis (Gene-based burden) 539 European ancestry cases, 331,215 European ancestry controls NA Illumina [184201] 0 tendinitis http://purl.obolibrary.org/obo/MONDO_0004857 GCST90081949 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Very often true (UKB data field 20489) 72,864 European ancestry cases, 66,332 European ancestry controls NA Affymetrix, Illumina [240621] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078530 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Testicular problems (not cancer) (Gene-based burden) 628 European ancestry cases, 331,126 European ancestry controls NA Illumina [184200] 0 testicular disease http://www.ebi.ac.uk/efo/EFO_0009601 GCST90081706 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent inability to stop or control worrying - More than half the days (UKB data field 20509) 3,165 European ancestry cases, 135,984 European ancestry controls NA Affymetrix, Illumina [240581] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078572 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcium carbonate cholecalciferol (Gene-based burden) 750 European ancestry cases, 320,008 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082166 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic lymphocytic leukemia of B-cell type (UKB data field 40006) 571 European ancestry cases, 73,659 European ancestry controls 353 European ancestry cases, 122,673 European ancestry controls Affymetrix, Illumina [141235] 1 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90079124 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Ex smoker (UKB data field 22506) (Gene-based burden) 39,575 European ancestry cases, 68,133 European ancestry controls NA Illumina [165911] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082862 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - Most of the day (UKB data field 20436) 35,771 European ancestry cases, 38,421 European ancestry controls NA Affymetrix, Illumina [141393] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078453 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Never smoked (UKB data field 22506) (Gene-based burden) 63,909 European ancestry cases, 43,799 European ancestry controls NA Illumina [165911] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082863 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of bladder (UKB data field 40006) 721 European ancestry cases, 73,509 European ancestry controls NA Affymetrix, Illumina [141236] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90079133 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Total bilirubin levels (UKB data field 30840) (Gene-based burden) 410,431 European ancestry individuals NA Illumina [185654] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90083027 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of other and unspecified genital organs (UKB data field 40006) 593 European ancestry cases, 73,637 European ancestry controls NA Affymetrix, Illumina [141236] 0 urogenital neoplasm http://www.ebi.ac.uk/efo/EFO_0003863 GCST90079132 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Total protein levels (UKB data field 30860) (Gene-based burden) 377,964 European ancestry individuals NA Illumina [185104] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90083029 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of other and unspecified sites (UKB data field 40006) 776 European ancestry cases, 73,454 European ancestry controls NA Affymetrix, Illumina [141236] 0 carcinoma http://www.ebi.ac.uk/efo/EFO_0000313 GCST90079134 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Touchscreen duration (UKB data field 630) (Gene-based burden) 430,751 European ancestry individuals NA Illumina [185946] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90083477 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of skin (UKB data field 40006) 1,322 European ancestry cases, 72,908 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079127 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Townsend deprivation index at recruitment (UKB data field 189) (Gene-based burden) 430,494 European ancestry individuals NA Illumina [185950] 0 Townsend deprivation index http://www.ebi.ac.uk/efo/EFO_0009711 GCST90081603 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diffuse large B-cell lymphoma (UKB data field 40006) 672 European ancestry cases, 73,558 European ancestry controls NA Affymetrix, Illumina [141236] 0 diffuse large B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000403 GCST90079119 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Abandoned (UKB data field 20246) (Gene-based burden) 4,329 European ancestry cases, 102,771 European ancestry controls NA Illumina [166242] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082371 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of lower limb, including hip (UKB data field 40006) 1,075 European ancestry cases, 73,155 European ancestry controls NA Affymetrix, Illumina [141236] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079091 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Completed (UKB data field 20246) (Gene-based burden) 92,699 European ancestry cases, 14,401 European ancestry controls NA Illumina [166242] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082370 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of skin (UKB data field 40006) 3,349 European ancestry cases, 70,881 European ancestry controls NA Affymetrix, Illumina [141236] 1 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079092 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Completed with pause (UKB data field 20246) (Gene-based burden) 2,821 European ancestry cases, 104,279 European ancestry controls NA Illumina [166242] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082372 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of trunk (UKB data field 40006) 1,039 European ancestry cases, 73,191 European ancestry controls NA Affymetrix, Illumina [141236] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079089 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcium salts (Gene-based burden) 2,735 European ancestry cases, 318,023 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082043 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lymphoid leukemia (UKB data field 40006) 699 European ancestry cases, 73,531 European ancestry controls 457 European ancestry cases, 122,673 European ancestry controls Affymetrix, Illumina [141235] 1 lymphoid leukemia http://www.ebi.ac.uk/efo/EFO_0004289 GCST90079125 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcium vitamin d (Gene-based burden) 2,081 European ancestry cases, 318,677 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081981 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Feelings of worthlessness during worst period of depression (UKB data field 20450) 37,621 European ancestry cases, 36,176 European ancestry controls NA Affymetrix, Illumina [140718] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078471 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - candesartan cilexetil (Gene-based burden) 5,111 European ancestry cases, 315,647 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082173 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia - left eye (UKB data field 5843) 2,871 European ancestry cases, 48,264 European ancestry controls NA Affymetrix, Illumina [102346] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90079389 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flixonase aqueous nasal spray (Gene-based burden) 1,837 European ancestry cases, 318,921 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082065 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia - right eye (UKB data field 5843) 3,062 European ancestry cases, 48,073 European ancestry controls NA Affymetrix, Illumina [102346] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90079388 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flixotide inhaler (Gene-based burden) 747 European ancestry cases, 320,011 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082010 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of unenthusiasm/disinterest (UKB data field 5375) 49,039 European ancestry individuals NA Affymetrix, Illumina [98525] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90079344 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Scarlet fever scarlatina (Gene-based burden) 1,058 European ancestry cases, 330,696 European ancestry controls NA Illumina [184201] 0 scarlet fever http://www.ebi.ac.uk/efo/EFO_0007477 GCST90081978 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ankle spacing width right (UKB data field 4119) (Gene-based burden) 166,358 European ancestry individuals NA Illumina [176168] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90083140 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had prolonged feelings of sadness or depression (UKB data field 20446) 76,460 European ancestry cases, 62,905 European ancestry controls NA Affymetrix, Illumina [240812] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078467 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A38: scarlet fever scarlatina (Gene-based burden) 936 European ancestry cases, 328,116 European ancestry controls NA Illumina [184145] 0 scarlet fever http://www.ebi.ac.uk/efo/EFO_0007477 GCST90081979 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever had prolonged loss of interest in normal activities (UKB data field 20441) 55,126 European ancestry cases, 84,200 European ancestry controls NA Affymetrix, Illumina [240792] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078465 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sciatica (Gene-based burden) 4,982 European ancestry cases, 326,772 European ancestry controls NA Illumina [184201] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90081873 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Never true (UKB data field 20487) 118,008 European ancestry cases, 21,317 European ancestry controls NA Affymetrix, Illumina [240775] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078521 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: sciatica (Gene-based burden) 4,079 European ancestry cases, 324,973 European ancestry controls NA Illumina [184145] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90081874 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Often (UKB data field 20487) 2,135 European ancestry cases, 137,190 European ancestry controls NA Affymetrix, Illumina [240775] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078524 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Shingles (Gene-based burden) 1,180 European ancestry cases, 330,574 European ancestry controls NA Illumina [184201] 0 susceptibility to shingles measurement http://www.ebi.ac.uk/efo/EFO_0008401 GCST90081937 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Rarely true (UKB data field 20487) 8,351 European ancestry cases, 130,974 European ancestry controls NA Affymetrix, Illumina [240775] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078522 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B02: shingles (Gene-based burden) 880 European ancestry cases, 328,172 European ancestry controls NA Illumina [184145] 0 susceptibility to shingles measurement http://www.ebi.ac.uk/efo/EFO_0008401 GCST90081938 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Sometimes true (UKB data field 20487) 9,087 European ancestry cases, 130,238 European ancestry controls NA Affymetrix, Illumina [240775] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078523 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleep apnoea (Gene-based burden) 1,594 European ancestry cases, 330,160 European ancestry controls NA Illumina [184201] 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90081667 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Very often true (UKB data field 20487) 1,744 European ancestry cases, 137,581 European ancestry controls NA Affymetrix, Illumina [240775] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078525 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47: sleep apnoea (Gene-based burden) 1,429 European ancestry cases, 327,623 European ancestry controls NA Illumina [184145] 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90081668 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever believed in unreal communications or signs (UKB data field 20474) 982 European ancestry cases, 138,332 European ancestry controls NA Affymetrix, Illumina [240767] 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST90078508 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spinal injury (Gene-based burden) 730 European ancestry cases, 331,024 European ancestry controls NA Illumina [184201] 0 Spinal cord injury http://www.ebi.ac.uk/efo/EFO_1001919 GCST90081734 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Recent trouble relaxing - More than half the days (UKB data field 20515) 4,031 European ancestry cases, 135,255 European ancestry controls NA Affymetrix, Illumina [240761] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078593 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Spine arthritis or spondylitis (Gene-based burden) 4,039 European ancestry cases, 327,715 European ancestry controls NA Illumina [184201] 0 spondylitis http://purl.obolibrary.org/obo/MONDO_0003937 GCST90081767 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at first episode of depression (UKB data field 20433) 72,485 European ancestry individuals NA Affymetrix, Illumina [138470] 0 unipolar depression, age at onset http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90078449 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - cerazette (Gene-based burden) 1,103 European ancestry cases, 319,655 European ancestry controls NA Illumina [183962] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082206 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 25 (UKB data field 20179) 8,154 European ancestry cases, 63,427 European ancestry controls NA Affymetrix, Illumina [136932] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078353 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - cetirizine (Gene-based burden) 5,250 European ancestry cases, 315,508 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082094 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 26 (UKB data field 20179) 54,304 European ancestry cases, 17,277 European ancestry controls NA Affymetrix, Illumina [136932] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078354 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - chondroitin product (Gene-based burden) 5,753 European ancestry cases, 315,005 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082219 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 27 (UKB data field 20179) 4,127 European ancestry cases, 67,454 European ancestry controls NA Affymetrix, Illumina [136932] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078355 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - citalopram (Gene-based burden) 7,990 European ancestry cases, 312,768 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082139 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 28 (UKB data field 20179) 1,989 European ancestry cases, 69,592 European ancestry controls NA Affymetrix, Illumina [136932] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078356 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - clonidine (Gene-based burden) 589 European ancestry cases, 320,169 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082093 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 29 (UKB data field 20179) 3,007 European ancestry cases, 68,574 European ancestry controls NA Affymetrix, Illumina [136932] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078357 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - clopidogrel (Gene-based burden) 3,279 European ancestry cases, 317,479 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082183 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Feelings of tiredness during worst episode of depression (UKB data field 20449) 58,240 European ancestry cases, 12,695 European ancestry controls NA Affymetrix, Illumina [135991] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90078470 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - co-codamol (Gene-based burden) 10,402 European ancestry cases, 310,356 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082147 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain or discomfort walking normally (UKB data field 3606) 12,469 European ancestry cases, 58,080 European ancestry controls NA Affymetrix, Illumina [135631] 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90079066 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - co-dydramol (Gene-based burden) 2,752 European ancestry cases, 318,006 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082148 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hormone replacement therapy last use (age of onset) (UKB data field 3546) 70,090 European ancestry individuals NA Affymetrix, Illumina [134117] 0 age at onset, hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0004847, http://www.ebi.ac.uk/efo/EFO_0003961 GCST90079062 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - coenzyme q10/ubiquinone bio-quinone/coenzyme q10 (Gene-based burden) 1,629 European ancestry cases, 319,129 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082220 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood pressure medication (UKB data field 6177) 51,432 European ancestry cases, 18,041 European ancestry controls NA Affymetrix, Illumina [133985] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079487 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - co-tenidone (Gene-based burden) 615 European ancestry cases, 320,143 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082146 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cholesterol lowering medication use (UKB data field 6177) 49,091 European ancestry cases, 20,382 European ancestry controls NA Affymetrix, Illumina [133985] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90079486 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - cod liver oil (Gene-based burden) 25,871 European ancestry cases, 294,887 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082120 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Insulin levels (UKB data field 6177) 2,807 European ancestry cases, 66,666 European ancestry controls NA Affymetrix, Illumina [133985] 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90079488 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - codeine (Gene-based burden) 2,430 European ancestry cases, 318,328 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082101 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty concentrating during worst depression (UKB data field 20435) 54,939 European ancestry cases, 14,785 European ancestry controls NA Affymetrix, Illumina [133944] 0 decreased concentration http://purl.obolibrary.org/obo/PATO_0001163 GCST90078450 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evening primrose oil product (Gene-based burden) 992 European ancestry cases, 319,766 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082223 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - long (UKB data field 5556) 1,542 European ancestry cases, 53,298 European ancestry controls NA Affymetrix, Illumina [108508] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079361 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evorel 25 patch (Gene-based burden) 696 European ancestry cases, 320,062 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082138 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - metres (UKB data field 5556) 32,325 European ancestry cases, 22,515 European ancestry controls NA Affymetrix, Illumina [108508] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079362 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evorel conti patch (Gene-based burden) 528 European ancestry cases, 320,230 European ancestry controls NA Illumina [183959] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082168 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - tall (UKB data field 5556) 21,880 European ancestry cases, 32,960 European ancestry controls NA Affymetrix, Illumina [108508] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079363 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ezetimibe (Gene-based burden) 2,675 European ancestry cases, 318,083 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082212 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Not at all (UKB data field 4814) 18,338 European ancestry cases, 35,357 European ancestry controls NA Affymetrix, Illumina [106901] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079227 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ezetrol (Gene-based burden) 843 European ancestry cases, 319,915 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082213 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Severely (UKB data field 4814) 1,664 European ancestry cases, 52,031 European ancestry controls NA Affymetrix, Illumina [106901] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079224 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - felodipine (Gene-based burden) 3,832 European ancestry cases, 316,926 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082117 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Moderately (UKB data field 4814) 8,948 European ancestry cases, 44,747 European ancestry controls NA Affymetrix, Illumina [106901] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079225 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - femoston (Gene-based burden) 712 European ancestry cases, 320,046 European ancestry controls NA Illumina [183937] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082143 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Slightly (UKB data field 4814) 26,815 European ancestry cases, 26,880 European ancestry controls NA Affymetrix, Illumina [106901] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90079226 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fenofibrate (Gene-based burden) 614 European ancestry cases, 320,144 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081994 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleeping too much (UKB data field 20534) 11,243 European ancestry cases, 42,867 European ancestry controls NA Affymetrix, Illumina [106788] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90078616 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ferrous sulphate (Gene-based burden) 2,261 European ancestry cases, 318,497 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082040 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling asleep (UKB data field 20533) 41,090 European ancestry cases, 13,020 European ancestry controls NA Affymetrix, Illumina [106788] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90078615 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - fexofenadine (Gene-based burden) 1,530 European ancestry cases, 319,228 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082165 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Waking too early (UKB data field 20535) 41,019 European ancestry cases, 13,091 European ancestry controls NA Affymetrix, Illumina [106788] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90078617 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - finasteride (Gene-based burden) 1,878 European ancestry cases, 318,880 European ancestry controls NA Illumina [183958] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082034 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hip pain for three months (UKB data field 3414) 40,643 European ancestry cases, 11,498 European ancestry controls NA Affymetrix, Illumina [103650] 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90079055 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flax oil (Gene-based burden) 731 European ancestry cases, 320,027 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082131 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Myopia - both eyes (UKB data field 5843) 45,679 European ancestry cases, 5,456 European ancestry controls NA Affymetrix, Illumina [102346] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90079390 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - flecainide (Gene-based burden) 755 European ancestry cases, 320,003 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082116 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - colofac (Gene-based burden) 554 European ancestry cases, 320,204 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082181 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Numeric memory - Time to complete test (UKB data field 4285) 67,473 European ancestry individuals NA Affymetrix, Illumina [131071] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079169 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dermovate cream (Gene-based burden) 697 European ancestry cases, 320,061 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082090 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleep change (UKB data field 20532) 54,110 European ancestry cases, 13,718 European ancestry controls NA Affymetrix, Illumina [130645] 0 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST90078614 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - desloratadine (Gene-based burden) 579 European ancestry cases, 320,179 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082191 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Both gained and lost some weight during the episode (UKB data field 20536) 4,299 European ancestry cases, 62,954 European ancestry controls NA Affymetrix, Illumina [129542] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078621 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - detrusitol (Gene-based burden) 685 European ancestry cases, 320,073 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082177 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Gained weight (UKB data field 20536) 11,709 European ancestry cases, 55,544 European ancestry controls NA Affymetrix, Illumina [129542] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078619 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diazepam (Gene-based burden) 1,211 European ancestry cases, 319,547 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082008 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Lost weight (UKB data field 20536) 24,070 European ancestry cases, 43,183 European ancestry controls NA Affymetrix, Illumina [129542] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078620 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diclofenac (Gene-based burden) 9,113 European ancestry cases, 311,645 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082103 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Weight change during worst episode of depression - Stayed about the same or was on a diet (UKB data field 20536) 27,175 European ancestry cases, 40,078 European ancestry controls NA Affymetrix, Illumina [129542] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90078618 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dicloflex (Gene-based burden) 512 European ancestry cases, 320,246 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082141 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Oestradiol levels (UKB data field 30800) 66,773 European ancestry individuals NA Affymetrix, Illumina [128746] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90079036 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - digoxin (Gene-based burden) 1,185 European ancestry cases, 319,573 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082226 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - micronor tablet 612 European ancestry cases, 320,146 European ancestry controls NA Affymetrix, Illumina [126939] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90078050 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dihydrocodeine (Gene-based burden) 1,534 European ancestry cases, 319,224 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082102 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - A little bit (UKB data field 20496) 18,130 European ancestry cases, 44,686 European ancestry controls NA Affymetrix, Illumina [122263] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078542 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diltiazem (Gene-based burden) 909 European ancestry cases, 319,849 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082082 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - Extremely (UKB data field 20496) 1,009 European ancestry cases, 61,807 European ancestry controls NA Affymetrix, Illumina [122263] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078545 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - diprobase cream (Gene-based burden) 742 European ancestry cases, 320,016 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082068 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - Moderately (UKB data field 20496) 4,193 European ancestry cases, 58,623 European ancestry controls NA Affymetrix, Illumina [122263] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078543 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dipyridamole (Gene-based burden) 814 European ancestry cases, 319,944 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081991 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - Quite a bit (UKB data field 20496) 3,396 European ancestry cases, 59,420 European ancestry controls NA Affymetrix, Illumina [122263] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90078544 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - domperidone (Gene-based burden) 908 European ancestry cases, 319,850 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082071 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt irritable or had angry outbursts in past month - A little bit (UKB data field 20494) 20,254 European ancestry cases, 42,559 European ancestry controls NA Affymetrix, Illumina [122258] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078535 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dosulepin (Gene-based burden) 1,535 European ancestry cases, 319,223 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082125 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt irritable or had angry outbursts in past month - Moderately (UKB data field 20494) 3,089 European ancestry cases, 59,724 European ancestry controls NA Affymetrix, Illumina [122258] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078536 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - dovobet ointment (Gene-based burden) 536 European ancestry cases, 320,222 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082199 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt irritable or had angry outbursts in past month - Quite a bit (UKB data field 20494) 1,761 European ancestry cases, 61,052 European ancestry controls NA Affymetrix, Illumina [122258] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078537 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - doxazosin (Gene-based burden) 5,111 European ancestry cases, 315,647 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082079 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain or discomfort when walking uphill or hurrying (UKB data field 3751) 15,414 European ancestry cases, 41,575 European ancestry controls NA Affymetrix, Illumina [112283] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90079071 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - elleste duet conti (Gene-based burden) 927 European ancestry cases, 319,831 European ancestry controls NA Illumina [183959] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082172 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm regularity index right (UKB data field 5161) 56,694 European ancestry individuals NA Affymetrix, Illumina [112104] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079316 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - elleste solo (Gene-based burden) 783 European ancestry cases, 319,975 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082150 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry angle right (UKB data field 5109) 56,612 European ancestry individuals NA Affymetrix, Illumina [111961] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079287 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - enalapril (Gene-based burden) 3,349 European ancestry cases, 317,409 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082114 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry index right (UKB data field 5158) 56,612 European ancestry individuals NA Affymetrix, Illumina [111961] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079313 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - epilim (Gene-based burden) 701 European ancestry cases, 320,057 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082053 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm regularity index left (UKB data field 5162) 55,532 European ancestry individuals NA Affymetrix, Illumina [110268] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079317 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - escitalopram (Gene-based burden) 807 European ancestry cases, 319,951 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082201 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry angle left (UKB data field 5110) 55,503 European ancestry individuals NA Affymetrix, Illumina [110219] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079288 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - esomeprazole (Gene-based burden) 1,565 European ancestry cases, 319,193 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082196 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 6mm asymmetry index left (UKB data field 5157) 55,503 European ancestry individuals NA Affymetrix, Illumina [110219] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079312 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - estraderm mx 25 patch (Gene-based burden) 666 European ancestry cases, 320,092 European ancestry controls NA Illumina [183957] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082152 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Presbyopia - both eyes (UKB data field 5610) 49,647 European ancestry cases, 5,658 European ancestry controls NA Affymetrix, Illumina [108903] 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90079366 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - estradiol product (Gene-based burden) 888 European ancestry cases, 319,870 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082202 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Presbyopia - left eye (UKB data field 5610) 3,048 European ancestry cases, 52,257 European ancestry controls NA Affymetrix, Illumina [108903] 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90079365 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - evening primrose oil (Gene-based burden) 6,997 European ancestry cases, 313,761 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082137 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Presbyopia - right eye (UKB data field 5610) 3,113 European ancestry cases, 52,192 European ancestry controls NA Affymetrix, Illumina [108903] 0 presbyopia http://purl.obolibrary.org/obo/MONDO_0001330 GCST90079364 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79.8: Secondary malignant neoplasm of other specified sites 1,374 European ancestry cases, 386,553 European ancestry controls NA Affymetrix, Illumina [510683] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079628 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Haemoglobin concentration (UKB data field 30020) (Gene-based burden) 419,192 European ancestry individuals NA Illumina [185803] 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90082966 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C91.1: Chronic lymphocytic leukemia of B-cell type 669 European ancestry cases, 387,257 European ancestry controls 353 European ancestry cases, 122,673 European ancestry controls Affymetrix, Illumina [510683] 1 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90079641 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 1 (UKB data field 2395) (Gene-based burden) 63,607 European ancestry cases, 132,262 European ancestry controls NA Illumina [177396] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90082930 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.1: Other benign neoplasm of skin of eyelid, including canthus 1,342 European ancestry cases, 386,579 European ancestry controls NA Affymetrix, Illumina [510683] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079678 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 2 (UKB data field 2395) (Gene-based burden) 46,649 European ancestry cases, 149,220 European ancestry controls NA Illumina [177396] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90082931 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05.0: Thyrotoxicosis with diffuse goiter 565 European ancestry cases, 387,358 European ancestry controls NA Affymetrix, Illumina [510683] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90079727 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 3 (UKB data field 2395) (Gene-based burden) 54,082 European ancestry cases, 141,787 European ancestry controls NA Illumina [177396] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90082932 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04.1: Other disorders of lacrimal gland 520 European ancestry cases, 387,404 European ancestry controls NA Affymetrix, Illumina [510683] 0 disorder of lacrimal gland http://purl.obolibrary.org/obo/MONDO_0024625 GCST90079875 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair balding pattern - Pattern 4 (UKB data field 2395) (Gene-based burden) 37,404 European ancestry cases, 158,465 European ancestry controls NA Illumina [177396] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90082933 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I77.1: Stricture of artery 1,043 European ancestry cases, 386,876 European ancestry controls NA Affymetrix, Illumina [510683] 0 stricture http://www.ebi.ac.uk/efo/EFO_0006818 GCST90080054 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Black (UKB data field 1747) (Gene-based burden) 20,623 European ancestry cases, 409,356 European ancestry controls NA Illumina [185934] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90081596 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J38.3: Other diseases of vocal cords 730 European ancestry cases, 387,195 European ancestry controls NA Affymetrix, Illumina [510683] 0 Vocal cord dysfunction http://purl.obolibrary.org/obo/HP_0031801 GCST90080120 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Blonde (UKB data field 1747) (Gene-based burden) 48,595 European ancestry cases, 381,384 European ancestry controls NA Illumina [185935] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90081592 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J95: Intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified 523 European ancestry cases, 387,401 European ancestry controls NA Affymetrix, Illumina [510683] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080154 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Dark brown (UKB data field 1747) (Gene-based burden) 164,398 European ancestry cases, 265,581 European ancestry controls NA Illumina [185935] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90081595 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.5: Polyp of colon 15,366 European ancestry cases, 372,559 European ancestry controls NA Affymetrix, Illumina [510683] 0 polyp of colon http://purl.obolibrary.org/obo/MONDO_0021400 GCST90080271 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Light brown (UKB data field 1747) (Gene-based burden) 175,455 European ancestry cases, 254,524 European ancestry controls NA Illumina [185935] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90081594 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N21.0: Calculus in bladder 886 European ancestry cases, 387,039 European ancestry controls NA Affymetrix, Illumina [510683] 0 bladder calculus http://www.ebi.ac.uk/efo/EFO_1000839 GCST90080589 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Other (UKB data field 1747) (Gene-based burden) 5,564 European ancestry cases, 424,415 European ancestry controls NA Illumina [185935] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90081597 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30.8: Other cystitis 753 European ancestry cases, 387,172 European ancestry controls NA Affymetrix, Illumina [510683] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90080597 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hair colour natural before greying - Red (UKB data field 1747) (Gene-based burden) 19,553 European ancestry cases, 410,426 European ancestry controls NA Illumina [185935] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90081593 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z04.3: Encounter for examination and observation following other accident 524 European ancestry cases, 387,401 European ancestry controls NA Affymetrix, Illumina [510683] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081194 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hand grip strength left (UKB data field 46) (Gene-based burden) 429,288 European ancestry individuals NA Illumina [185926] 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90083202 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G63: Polyneuropathy in diseases classified elsewhere 586 European ancestry cases, 387,338 European ancestry controls NA Affymetrix, Illumina [510682] 0 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90079852 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hand grip strength right (UKB data field 47) (Gene-based burden) 429,337 European ancestry individuals NA Illumina [185919] 0 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90083205 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I70.20: Unspecified atherosclerosis of native arteries of extremities 509 European ancestry cases, 387,414 European ancestry controls NA Affymetrix, Illumina [510682] 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90080044 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Handedness chirality laterality - Left handed (UKB data field 1707) (Gene-based burden) 41,056 European ancestry cases, 389,556 European ancestry controls NA Illumina [185943] 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90081581 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K05.3: Chronic periodontitis 652 European ancestry cases, 387,269 European ancestry controls NA Affymetrix, Illumina [510682] 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90080169 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Handedness chirality laterality - Right handed (UKB data field 1707) (Gene-based burden) 382,514 European ancestry cases, 48,098 European ancestry controls NA Illumina [185943] 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90081580 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50.9: Crohn's disease, unspecified 1,697 European ancestry cases, 386,228 European ancestry controls NA Affymetrix, Illumina [510682] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90080231 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Handedness chirality laterality - Use both right and left hands equally (UKB data field 1707) (Gene-based burden) 7,455 European ancestry cases, 423,157 European ancestry controls NA Illumina [185943] 0 functional laterality http://www.ebi.ac.uk/efo/EFO_0003889 GCST90081582 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.1: Rectal polyp 8,321 European ancestry cases, 379,602 European ancestry controls NA Affymetrix, Illumina [510682] 0 polyp of rectum http://purl.obolibrary.org/obo/MONDO_0021398 GCST90080263 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Extremely happy (UKB data field 4526) (Gene-based burden) 10,779 European ancestry cases, 166,237 European ancestry controls NA Illumina [177117] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90083162 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.1: Perforation of intestine (nontraumatic) 528 European ancestry cases, 387,395 European ancestry controls NA Affymetrix, Illumina [510682] 0 intestinal perforation http://www.ebi.ac.uk/efo/EFO_1000987 GCST90080269 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Happiness - Moderately happy (UKB data field 4526) (Gene-based burden) 92,186 European ancestry cases, 84,830 European ancestry controls NA Illumina [177117] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90083164 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat percentage right (UKB data field 23119) 423,608 European ancestry individuals NA Affymetrix, Illumina [542282] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90078922 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Anticoagulant medicine use (Gene-based burden) 9,858 European ancestry cases, 310,900 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90085441 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat mass right (UKB data field 23120) 423,576 European ancestry individuals NA Affymetrix, Illumina [542252] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90078923 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ischemic stroke (Gene-based burden) 6,260 European ancestry cases, 270,409 European ancestry controls NA Illumina [182653] 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90085442 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat free mass right (UKB data field 23121) 423,573 European ancestry individuals NA Affymetrix, Illumina [542247] 3 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90078924 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stroke (Gene-based burden) 18,075 European ancestry cases, 272,229 European ancestry controls NA Illumina [183101] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90085443 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm predicted mass right (UKB data field 23122) 423,566 European ancestry individuals NA Affymetrix, Illumina [542238] 3 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90078925 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Aortic stenosis (Gene-based burden) 3,900 European ancestry cases, 300,255 European ancestry controls NA Illumina [183543] 0 aortic stenosis http://www.ebi.ac.uk/efo/EFO_0000266 GCST90085444 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat percentage left (UKB data field 23123) 423,545 European ancestry individuals NA Affymetrix, Illumina [542222] 0 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90078926 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Apolipoprotein A levels (UKB data field 30630) (Gene-based burden) 376,129 European ancestry individuals NA Illumina [185060] 0 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90083002 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat mass left (UKB data field 23124) 423,512 European ancestry individuals NA Affymetrix, Illumina [542194] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90078927 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Apolipoprotein B levels (UKB data field 30640) (Gene-based burden) 410,113 European ancestry individuals NA Illumina [185647] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90083004 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat free mass left (UKB data field 23125) 423,502 European ancestry individuals NA Affymetrix, Illumina [542186] 3 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90078928 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Arm fat free mass left (UKB data field 23125) (Gene-based burden) 423,502 European ancestry individuals NA Illumina [185858] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90082914 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X59: Exposure to unspecified factor as an external cause of morbidity and mortality 4,394 European ancestry cases, 383,536 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081137 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 Z score (UKB data field 20256) (Gene-based burden) 343,302 European ancestry individuals NA Illumina [184375] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90082374 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - Once a week (UKB data field 971) (Gene-based burden) 59,744 European ancestry cases, 253,140 European ancestry controls NA Illumina [183670] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083507 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K42.9: Umbilical hernia without obstruction or gangrene 4,355 European ancestry cases, 383,572 European ancestry controls NA Affymetrix, Illumina [510686] 0 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90080223 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - Once in the last 4 weeks (UKB data field 971) (Gene-based burden) 25,277 European ancestry cases, 287,607 European ancestry controls NA Illumina [183670] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083505 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K55.2: Angiodysplasia of colon 619 European ancestry cases, 387,311 European ancestry controls NA Affymetrix, Illumina [510686] 0 Gastrointestinal angiodysplasia http://purl.obolibrary.org/obo/HP_0000471 GCST90080238 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - 2 to 3 times in the last 4 weeks (UKB data field 971) (Gene-based burden) 95,935 European ancestry cases, 216,949 European ancestry controls NA Illumina [183670] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083506 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K61.0: Anal abscess 1,292 European ancestry cases, 386,634 European ancestry controls NA Affymetrix, Illumina [510686] 0 Rectal abscess http://purl.obolibrary.org/obo/HP_0005224 GCST90080260 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - 2 to 3 times a week (UKB data field 971) (Gene-based burden) 77,785 European ancestry cases, 235,099 European ancestry controls NA Illumina [183670] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083508 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K86.1: Other chronic pancreatitis 535 European ancestry cases, 387,394 European ancestry controls NA Affymetrix, Illumina [510686] 0 chronic pancreatitis http://www.ebi.ac.uk/efo/EFO_0000342 GCST90080311 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of walking for pleasure in last 4 weeks - 4 to 5 times a week (UKB data field 971) (Gene-based burden) 38,670 European ancestry cases, 274,214 European ancestry controls NA Illumina [183670] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90083509 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.8: Other internal derangements of knee 2,303 European ancestry cases, 385,622 European ancestry controls NA Affymetrix, Illumina [510686] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080446 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequent trouble falling or staying asleep during worst period of anxiety (UKB data field 20427) (Gene-based burden) 34,560 European ancestry cases, 7,692 European ancestry controls NA Illumina [137133] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90082430 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.7: Osteophyte 3,804 European ancestry cases, 384,122 European ancestry controls NA Affymetrix, Illumina [510686] 0 exostosis http://purl.obolibrary.org/obo/MONDO_0002181 GCST90080464 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Extremely happy (UKB data field 4570) (Gene-based burden) 25,041 European ancestry cases, 150,736 European ancestry controls NA Illumina [177003] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90083186 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51.3: Other thoracic, thoracolumbar and lumbosacral intervertebral disc degeneration 3,288 European ancestry cases, 384,639 European ancestry controls NA Affymetrix, Illumina [510686] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90080497 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Moderately happy (UKB data field 4570) (Gene-based burden) 57,135 European ancestry cases, 118,642 European ancestry controls NA Illumina [177003] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90083188 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M72.04: Palmar fascial fibromatosis [Dupuytren] 1,695 European ancestry cases, 386,235 European ancestry controls NA Affymetrix, Illumina [510686] 0 Palmar Fibromatosis http://www.ebi.ac.uk/efo/EFO_1000438 GCST90080529 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Moderately unhappy (UKB data field 4570) (Gene-based burden) 4,889 European ancestry cases, 170,888 European ancestry controls NA Illumina [177003] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90083189 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N03.9: Chronic nephritic syndrome with unspecified morphologic changes 918 European ancestry cases, 387,010 European ancestry controls NA Affymetrix, Illumina [510686] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90080572 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Very happy (UKB data field 4570) (Gene-based burden) 96,044 European ancestry cases, 79,733 European ancestry controls NA Illumina [177003] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90083187 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N17.9: Acute kidney failure, unspecified 7,852 European ancestry cases, 380,074 European ancestry controls NA Affymetrix, Illumina [510686] 0 acute kidney failure http://purl.obolibrary.org/obo/MONDO_0002492 GCST90080579 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Friendships satisfaction - Very unhappy (UKB data field 4570) (Gene-based burden) 792 European ancestry cases, 174,985 European ancestry controls NA Illumina [177003] 0 friendship satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009725 GCST90083190 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.8: Other specified disorders of urinary system 580 European ancestry cases, 387,349 European ancestry controls NA Affymetrix, Illumina [510686] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90080614 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gamma glutamyltransferase levels (UKB data field 30730) (Gene-based burden) 411,861 European ancestry individuals NA Illumina [185663] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90083014 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required left - none (UKB data field 6075) (Gene-based burden) 32,050 European ancestry cases, 49,766 European ancestry controls NA Illumina [160243] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083412 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.6: Other artificial openings of urinary tract status 543 European ancestry cases, 387,384 European ancestry controls NA Affymetrix, Illumina [510685] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081415 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required left - wearing (UKB data field 6075) (Gene-based burden) 45,986 European ancestry cases, 35,830 European ancestry controls NA Illumina [160243] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083413 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z95.4: Presence of other heart-valve replacement 1,277 European ancestry cases, 386,650 European ancestry controls NA Affymetrix, Illumina [510685] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081422 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required right - elsewhere (UKB data field 6074) (Gene-based burden) 4,185 European ancestry cases, 77,665 European ancestry controls NA Illumina [160258] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083411 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C71.9: Malignant neoplasm of brain, unspecified 550 European ancestry cases, 387,380 European ancestry controls NA Affymetrix, Illumina [510684] 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90079613 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required right - none (UKB data field 6074) (Gene-based burden) 32,052 European ancestry cases, 49,798 European ancestry controls NA Illumina [160258] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083409 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I69: Sequelae of cerebrovascular disease 1,714 European ancestry cases, 386,210 European ancestry controls NA Affymetrix, Illumina [510684] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90080043 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required right - wearing (UKB data field 6074) (Gene-based burden) 46,020 European ancestry cases, 35,830 European ancestry controls NA Illumina [160258] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083410 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.8: Other specified diseases of intestine 2,030 European ancestry cases, 385,889 European ancestry controls NA Affymetrix, Illumina [510684] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080272 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glucose levels (UKB data field 30740) (Gene-based burden) 377,948 European ancestry individuals NA Illumina [185096] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90083015 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K82.8: Other specified diseases of gallbladder 1,358 European ancestry cases, 386,568 European ancestry controls NA Affymetrix, Illumina [510684] 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90080303 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glycated haemoglobin HbA1c levels (UKB data field 30750) (Gene-based burden) 412,234 European ancestry individuals NA Illumina [185695] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90083016 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.32: Other meniscus derangements, posterior horn of medial meniscus 881 European ancestry cases, 387,049 European ancestry controls NA Affymetrix, Illumina [510684] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080440 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Guilty feelings (UKB data field 2030) (Gene-based burden) 125,294 European ancestry cases, 295,085 European ancestry controls NA Illumina [185826] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082381 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W23: Caught, crushed, jammed or pinched in or between objects 975 European ancestry cases, 386,952 European ancestry controls NA Affymetrix, Illumina [510684] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081122 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Helicobacter pylori - definition 1 (UKB data field 23073) (Gene-based burden) 1,472 European ancestry cases, 2,832 European ancestry controls NA Illumina [45424] 0 Helicobacter pylori seropositivity http://www.ebi.ac.uk/efo/EFO_0009341 GCST90082886 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z00.0: Encounter for general adult medical examination 561 European ancestry cases, 387,369 European ancestry controls NA Affymetrix, Illumina [510684] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081178 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Seropositivity for Helicobacter pylori - definition 2 (UKB data field 23074) (Gene-based burden) 2,568 European ancestry cases, 5,973 European ancestry controls NA Illumina [70714] 0 Helicobacter pylori seropositivity http://www.ebi.ac.uk/efo/EFO_0009341 GCST90082887 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45: Encounter for adjustment and management of implanted device 4,136 European ancestry cases, 383,784 European ancestry controls 1,691 European ancestry cases, 105,359 European ancestry controls Affymetrix, Illumina [510684] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90081264 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Had major operations (UKB data field 2415) (Gene-based burden) 127,607 European ancestry cases, 68,219 European ancestry controls NA Illumina [177400] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90082934 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45.0: Encounter for adjustment and management of cardiac device 1,115 European ancestry cases, 386,805 European ancestry controls NA Affymetrix, Illumina [510684] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90081261 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Had other major operations (UKB data field 2844) (Gene-based burden) 157,226 European ancestry cases, 74,569 European ancestry controls NA Illumina [181061] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90082950 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C67.9: Malignant neoplasm of bladder, unspecified 2,407 European ancestry cases, 385,519 European ancestry controls NA Affymetrix, Illumina [510683] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90079611 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Haematocrit percentage (UKB data field 30030) (Gene-based burden) 419,193 European ancestry individuals NA Illumina [185803] 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90082967 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.60: Fracture of lateral malleolus 832 European ancestry cases, 387,098 European ancestry controls NA Affymetrix, Illumina [510686] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081023 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Extremely happy (UKB data field 20458) (Gene-based burden) 13,968 European ancestry cases, 124,983 European ancestry controls NA Illumina [172045] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082467 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T51.0: Toxic effect of ethanol 952 European ancestry cases, 386,976 European ancestry controls NA Affymetrix, Illumina [510686] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081062 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Moderately happy (UKB data field 20458) (Gene-based burden) 55,476 European ancestry cases, 83,475 European ancestry controls NA Illumina [172045] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082469 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T90: Sequelae of injuries of head 649 European ancestry cases, 387,281 European ancestry controls NA Affymetrix, Illumina [510686] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90081089 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Moderately unhappy (UKB data field 20458) (Gene-based burden) 6,122 European ancestry cases, 132,829 European ancestry controls NA Illumina [172045] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082470 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.0: Personal history of in-situ and benign neoplasms and neoplasms of uncertain behavior 6,926 European ancestry cases, 381,003 European ancestry controls 8,930 European ancestry cases, 32,200 European ancestry controls Affymetrix, Illumina [510686] 0 GCST90081355 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Very happy (UKB data field 20458) (Gene-based burden) 61,849 European ancestry cases, 77,102 European ancestry controls NA Illumina [172045] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082468 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.1: Acquired absence of breast and nipple 3,153 European ancestry cases, 384,776 European ancestry controls 449 European ancestry cases, 33,208 European ancestry controls Affymetrix, Illumina [510686] 0 mastectomy http://www.ebi.ac.uk/efo/EFO_0020987 GCST90081390 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness - Very unhappy (UKB data field 20458) (Gene-based burden) 1,178 European ancestry cases, 137,773 European ancestry controls NA Illumina [172045] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082471 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.3: Personal history of irradiation 4,774 European ancestry cases, 383,155 European ancestry controls 843 European ancestry cases, 34,688 European ancestry controls Affymetrix, Illumina [510686] 0 radiation exposure http://www.ebi.ac.uk/efo/EFO_0020980 GCST90081407 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Extremely happy (UKB data field 20459) (Gene-based burden) 12,364 European ancestry cases, 126,997 European ancestry controls NA Illumina [172114] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082472 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z94.8: Other transplanted organ and tissue status 513 European ancestry cases, 387,414 European ancestry controls NA Affymetrix, Illumina [510686] 0 transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005198 GCST90081417 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Extremely unhappy (UKB data field 20459) (Gene-based burden) 1,675 European ancestry cases, 137,686 European ancestry controls NA Illumina [172114] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082477 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.1: Dependence on respirator 567 European ancestry cases, 387,362 European ancestry controls NA Affymetrix, Illumina [510686] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081441 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Moderately happy (UKB data field 20459) (Gene-based burden) 57,988 European ancestry cases, 81,373 European ancestry controls NA Illumina [172114] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082474 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A04.7: Enterocolitis due to Clostridium difficile 881 European ancestry cases, 387,046 European ancestry controls NA Affymetrix, Illumina [510685] 0 clostridium difficile infection http://www.ebi.ac.uk/efo/EFO_0009130 GCST90079537 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Moderately unhappy (UKB data field 20459) (Gene-based burden) 12,672 European ancestry cases, 126,689 European ancestry controls NA Illumina [172114] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082475 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I22: Subsequent ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction 760 European ancestry cases, 387,165 European ancestry controls NA Affymetrix, Illumina [510685] 0 Subsequent ST elevation (STEMI) and non-ST elevation (NSTEMI) myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008584 GCST90079974 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Very happy (UKB data field 20459) (Gene-based burden) 51,255 European ancestry cases, 88,106 European ancestry controls NA Illumina [172114] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082473 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.1: Diverticular disease of small intestine without perforation or abscess 510 European ancestry cases, 387,411 European ancestry controls NA Affymetrix, Illumina [510685] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080245 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General happiness with own health - Very unhappy (UKB data field 20459) (Gene-based burden) 3,407 European ancestry cases, 135,954 European ancestry controls NA Illumina [172114] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082476 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28.1: Cyst of kidney, acquired 1,824 European ancestry cases, 386,102 European ancestry controls 3,347 European ancestry cases, 110,159 European ancestry controls Affymetrix, Illumina [510685] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90080592 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. General pain for three months (UKB data field 2956) (Gene-based burden) 5,909 European ancestry cases, 1,218 European ancestry controls NA Illumina [64154] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90082961 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T83.0: Mechanical complication of urinary catheter 575 European ancestry cases, 387,352 European ancestry controls NA Affymetrix, Illumina [510685] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081076 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - Most of the day (UKB data field 20436) (Gene-based burden) 35,771 European ancestry cases, 38,421 European ancestry controls NA Illumina [156064] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082439 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X64: Intentional self-poisoning by and exposure to other and unspecified drugs, medicaments and biological substances 659 European ancestry cases, 387,271 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081145 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fracture resulting from simple fall (UKB data field 3005) (Gene-based burden) 26,807 European ancestry cases, 17,827 European ancestry controls NA Illumina [139135] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90082970 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X65: Intentional self-poisoning by and exposure to alcohol 896 European ancestry cases, 387,034 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081146 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Ankle (UKB data field 6151) (Gene-based burden) 6,598 European ancestry cases, 38,595 European ancestry controls NA Illumina [139603] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083432 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y40: Adverse effects in the therapeutic use of systemic antibiotics 943 European ancestry cases, 386,987 European ancestry controls NA Affymetrix, Illumina [510688] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90081148 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Arm (UKB data field 6151) (Gene-based burden) 4,818 European ancestry cases, 40,375 European ancestry controls NA Illumina [139603] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083437 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y42: Adverse effects in the therapeutic use of hormones and their synthetic substitutes and antagonists, not elsewhere classified 1,110 European ancestry cases, 386,820 European ancestry controls NA Affymetrix, Illumina [510688] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90081149 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Hip (UKB data field 6151) (Gene-based burden) 823 European ancestry cases, 44,370 European ancestry controls NA Illumina [139603] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083434 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y43: Adverse effects in the therapeutic use of primarily systemic agents 3,135 European ancestry cases, 384,795 European ancestry controls NA Affymetrix, Illumina [510688] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90081151 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Leg (UKB data field 6151) (Gene-based burden) 3,016 European ancestry cases, 42,177 European ancestry controls NA Illumina [139603] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083433 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y43.3: Adverse effects in the therapeutic use of other antineoplastic drugs 2,845 European ancestry cases, 385,085 European ancestry controls NA Affymetrix, Illumina [510688] 0 response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0097327 GCST90081150 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Other bones (UKB data field 6151) (Gene-based burden) 24,623 European ancestry cases, 20,570 European ancestry controls NA Illumina [139603] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083438 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y45.0: Adverse effects in the therapeutic use of opioids and related analgesics 588 European ancestry cases, 387,342 European ancestry controls NA Affymetrix, Illumina [510688] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90081152 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Spine (UKB data field 6151) (Gene-based burden) 1,130 European ancestry cases, 44,063 European ancestry controls NA Illumina [139603] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083435 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y52: Adverse effects in the therapeutic use of agents primarily affecting the cardiovascular system 862 European ancestry cases, 387,068 European ancestry controls NA Affymetrix, Illumina [510688] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90081154 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bone sites - Wrist (UKB data field 6151) (Gene-based burden) 9,426 European ancestry cases, 35,767 European ancestry controls NA Illumina [139603] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083436 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y57: Adverse effects in the therapeutic use of other and unspecified drugs and medicaments 523 European ancestry cases, 387,407 European ancestry controls NA Affymetrix, Illumina [510688] 0 response to xenobiotic stimulus http://purl.obolibrary.org/obo/GO_0009410 GCST90081155 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured bones in last 5 years (UKB data field 2463) (Gene-based burden) 45,242 European ancestry cases, 383,540 European ancestry controls NA Illumina [185921] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90082937 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y60: Injury due to unintentional cut, puncture, perforation or haemorrhage during surgical and medical care 781 European ancestry cases, 387,149 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081157 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fractured heel right (UKB data field 4096) (Gene-based burden) 545 European ancestry cases, 169,917 European ancestry controls NA Illumina [176518] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90083133 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Y60.0: Injury due to unintentional cut, puncture, perforation or haemorrhage during surgical operation 628 European ancestry cases, 387,302 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081156 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.1: Encounter for antineoplastic chemotherapy and immunotherapy 12,171 European ancestry cases, 375,755 European ancestry controls 4,221 European ancestry cases, 98,179 European ancestry controls Affymetrix, Illumina [510685] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081279 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glasses worn required left - elsewhere (UKB data field 6075) (Gene-based burden) 4,188 European ancestry cases, 77,628 European ancestry controls NA Illumina [160243] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083414 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.1: Gastrostomy status 583 European ancestry cases, 387,340 European ancestry controls NA Affymetrix, Illumina [510685] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081412 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gestational diabetes only (UKB data field 4041) (Gene-based burden) 845 European ancestry cases, 7,001 European ancestry controls NA Illumina [68070] 0 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST90083128 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85.5: Mechanical complication of gastrointestinal prosthetic devices, implants and grafts 519 European ancestry cases, 387,408 European ancestry controls NA Affymetrix, Illumina [510685] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081084 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Fairly easy (UKB data field 1170) (Gene-based burden) 222,439 European ancestry cases, 207,750 European ancestry controls NA Illumina [185939] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90081557 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85.7: Infection and inflammatory reaction due to other internal prosthetic devices, implants and grafts 680 European ancestry cases, 387,244 European ancestry controls NA Affymetrix, Illumina [510685] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081085 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Not at all easy (UKB data field 1170) (Gene-based burden) 17,267 European ancestry cases, 412,922 European ancestry controls NA Illumina [185939] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90081555 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W29: Contact with other powered hand tools and household machinery 552 European ancestry cases, 387,377 European ancestry controls NA Affymetrix, Illumina [510685] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081125 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Not very easy (UKB data field 1170) (Gene-based burden) 62,083 European ancestry cases, 368,106 European ancestry controls NA Illumina [185939] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90081556 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z43: Encounter for attention to artificial openings 2,178 European ancestry cases, 385,749 European ancestry controls NA Affymetrix, Illumina [510685] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081260 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Getting up in morning - Very easy (UKB data field 1170) (Gene-based burden) 147,370 European ancestry cases, 282,819 European ancestry controls NA Illumina [185939] 0 ease of getting up in the morning, self-reported http://www.ebi.ac.uk/efo/EFO_0009817 GCST90081558 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L05: Pilonidal cyst and sinus 658 European ancestry cases, 386,608 European ancestry controls NA Affymetrix, Illumina [510128] 0 Pilonidal sinus http://purl.obolibrary.org/obo/HP_0010769 GCST90080332 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X59.9: Exposure to unspecified factor - Unspecified place 4,008 European ancestry cases, 383,922 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081136 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced vital capacity FVC (UKB data field 3062) (Gene-based burden) 395,451 European ancestry individuals NA Illumina [185485] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90083001 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X60: Intentional self-poisoning by and exposure to nonopioid analgesics, antipyretics and antirheumatics 1,572 European ancestry cases, 386,358 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081140 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced vital capacity FVC Best measure (UKB data field 20151) (Gene-based burden) 322,002 European ancestry individuals NA Illumina [183724] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90082303 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X60.0: Intentional self-poisoning by and exposure to nonopioid analgesics, antipyretics and antirheumatics - Home 761 European ancestry cases, 387,169 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081138 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced vital capacity FVC Z score (UKB data field 20257) (Gene-based burden) 343,302 European ancestry individuals NA Illumina [184375] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90082375 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X60.9: Intentional self-poisoning by and exposure to nonopioid analgesics, antipyretics and antirheumatics - Unspecified place 930 European ancestry cases, 387,000 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081139 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Former alcohol drinker (UKB data field 3731) (Gene-based burden) 15,969 European ancestry cases, 14,408 European ancestry controls NA Illumina [126522] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90083055 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X61: Intentional self-poisoning by and exposure to antiepileptic, sedative-hypnotic, antiparkinsonism and psychotropic drugs, not elsewhere classified 1,591 European ancestry cases, 386,339 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081143 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - About half of the day (UKB data field 20436) (Gene-based burden) 10,425 European ancestry cases, 63,767 European ancestry controls NA Illumina [156064] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082438 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X61.0: Intentional self-poisoning by and exposure to antiepileptic, sedative-hypnotic, antiparkinsonism and psychotropic drugs, not elsewhere classified - Home 814 European ancestry cases, 387,116 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081141 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - All day long (UKB data field 20436) (Gene-based burden) 18,434 European ancestry cases, 55,758 European ancestry controls NA Illumina [156064] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082440 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X61.9: Intentional self-poisoning by and exposure to antiepileptic, sedative-hypnotic, antiparkinsonism and psychotropic drugs, not elsewhere classified - Unspecified place 920 European ancestry cases, 387,010 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081142 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - Less than half of the day (UKB data field 20436) (Gene-based burden) 9,562 European ancestry cases, 64,630 European ancestry controls NA Illumina [156064] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082437 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X62: Intentional self-poisoning by and exposure to narcotics and psychodysleptics [hallucinogens], not elsewhere classified 559 European ancestry cases, 387,371 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081144 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Moderately happy (UKB data field 4581) (Gene-based burden) 80,442 European ancestry cases, 96,381 European ancestry controls NA Illumina [177071] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90083193 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W10.0: Fall on/from escalator 2,038 European ancestry cases, 385,891 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081106 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Moderately unhappy (UKB data field 4581) (Gene-based burden) 14,573 European ancestry cases, 162,250 European ancestry controls NA Illumina [177071] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90083194 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W11.0: Fall on/from ladder - Home 728 European ancestry cases, 387,202 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081109 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Very happy (UKB data field 4581) (Gene-based burden) 66,645 European ancestry cases, 110,178 European ancestry controls NA Illumina [177071] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90083192 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W11.9: Fall on/from ladder - Unspecified place 745 European ancestry cases, 387,185 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081110 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Very unhappy (UKB data field 4581) (Gene-based burden) 5,019 European ancestry cases, 171,804 European ancestry controls NA Illumina [177071] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90083195 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W18.0: Fall due to bumping against object 1,046 European ancestry cases, 386,883 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081113 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fluid intelligence completion status - Abandoned (UKB data field 20242) (Gene-based burden) 3,187 European ancestry cases, 106,707 European ancestry controls NA Illumina [166883] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082362 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W18.9: Unspecified place 638 European ancestry cases, 387,292 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081114 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fluid intelligence completion status - Completed (UKB data field 20242) (Gene-based burden) 96,202 European ancestry cases, 13,692 European ancestry controls NA Illumina [166883] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082361 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.0: Unspecified fall - Home 2,010 European ancestry cases, 385,920 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081116 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fluid intelligence completion status - Completed with pause (UKB data field 20242) (Gene-based burden) 10,505 European ancestry cases, 99,389 European ancestry controls NA Illumina [166883] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082363 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.2: Unspecified fall - School, other institution and public administrative area 518 European ancestry cases, 387,412 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081117 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Foot measured for bone density - left (UKB data field 3081) (Gene-based burden) 280,489 European ancestry cases, 3,638 European ancestry controls NA Illumina [182487] 0 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90083024 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.4: Unspecified fall - Street and highway 635 European ancestry cases, 387,295 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081118 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Foot measured for bone density - right (UKB data field 3081) (Gene-based burden) 3,638 European ancestry cases, 280,489 European ancestry controls NA Illumina [182487] 0 bone density http://www.ebi.ac.uk/efo/EFO_0003923 GCST90083025 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19.9: Unspecified fall - Unspecified place 3,891 European ancestry cases, 384,039 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081119 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 (UKB data field 3063) (Gene-based burden) 395,451 European ancestry individuals NA Illumina [185485] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90083003 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W44.9: Foreign body entering into or through eye or natural orifice causing accidental injury - Unspecified place 509 European ancestry cases, 387,421 European ancestry controls NA Affymetrix, Illumina [510688] 0 eye foreign body http://www.ebi.ac.uk/efo/EFO_1001322 GCST90081127 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 Best measure (UKB data field 20150) (Gene-based burden) 322,002 European ancestry individuals NA Illumina [183724] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90082302 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X50: Overexertion and strenuous or repetitive movements 1,283 European ancestry cases, 386,647 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081135 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 predicted (UKB data field 20153) (Gene-based burden) 136,823 European ancestry individuals NA Illumina [171456] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90082305 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 X50.9: Other and unspecified overexertion or strenuous movements or postures 509 European ancestry cases, 387,421 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081134 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 predicted percentage (UKB data field 20154) (Gene-based burden) 136,823 European ancestry individuals NA Illumina [171456] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90082306 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.2: Accidental puncture and laceration during a procedure, not elsewhere classified (T81.2) 1,820 European ancestry cases, 386,110 European ancestry controls NA Affymetrix, Illumina [510688] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081070 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 27 (UKB data field 5012) (Gene-based burden) 5,087 European ancestry cases, 92,983 European ancestry controls NA Illumina [163501] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083248 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.1: Mechanical complication of internal fixation device of bones of limb 1,002 European ancestry cases, 386,928 European ancestry controls NA Affymetrix, Illumina [510688] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081079 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 28 (UKB data field 5012) (Gene-based burden) 2,954 European ancestry cases, 95,116 European ancestry controls NA Illumina [163501] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083249 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T84.5: Infection and inflammatory reaction due to internal joint prosthesis 652 European ancestry cases, 387,277 European ancestry controls NA Affymetrix, Illumina [510688] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081080 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 29 (UKB data field 5012) (Gene-based burden) 4,869 European ancestry cases, 93,201 European ancestry controls NA Illumina [163501] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083250 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T85.8: Other specified complications of internal prosthetic devices, implants and grafts, not elsewhere classified 589 European ancestry cases, 387,341 European ancestry controls NA Affymetrix, Illumina [510688] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081086 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - long (UKB data field 20181) (Gene-based burden) 546 European ancestry cases, 28,784 European ancestry controls NA Illumina [121786] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082344 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T92: Sequelae of injuries of upper limb 835 European ancestry cases, 387,095 European ancestry controls NA Affymetrix, Illumina [510688] 0 limb injury http://www.ebi.ac.uk/efo/EFO_0009509 GCST90081090 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - long (UKB data field 5556) (Gene-based burden) 1,542 European ancestry cases, 53,298 European ancestry controls NA Illumina [145702] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083347 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T93: Sequelae of injuries of lower limb 975 European ancestry cases, 386,955 European ancestry controls NA Affymetrix, Illumina [510688] 0 limb injury http://www.ebi.ac.uk/efo/EFO_0009509 GCST90081091 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - metres (UKB data field 20181) (Gene-based burden) 19,284 European ancestry cases, 10,046 European ancestry controls NA Illumina [121786] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082345 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 U80: Agent resistant to penicillin and related antibiotics 876 European ancestry cases, 387,054 European ancestry controls NA Affymetrix, Illumina [510688] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081092 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - metres (UKB data field 5556) (Gene-based burden) 32,325 European ancestry cases, 22,515 European ancestry controls NA Illumina [145702] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083348 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V18.4: Pedal cycle driver injured in noncollision transport accident in traffic accident 591 European ancestry cases, 387,339 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081093 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - tall (UKB data field 20181) (Gene-based burden) 9,336 European ancestry cases, 19,994 European ancestry controls NA Illumina [121786] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082346 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V43: Car occupant injured in collision with car, pick-up truck or van 726 European ancestry cases, 387,204 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081096 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - tall (UKB data field 5556) (Gene-based burden) 21,880 European ancestry cases, 32,960 European ancestry controls NA Illumina [145702] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083349 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 V43.5: Car driver injured in collision with car, pick-up truck or van in traffic accident 520 European ancestry cases, 387,410 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081095 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prospective memory - Final attempt correct (UKB data field 4294) (Gene-based burden) 169,042 European ancestry cases, 7,158 European ancestry controls NA Illumina [177015] 0 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90083161 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W00.9: Unspecified fall due to ice and snow 617 European ancestry cases, 387,313 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081099 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Extremely happy (UKB data field 4581) (Gene-based burden) 17,249 European ancestry cases, 159,574 European ancestry controls NA Illumina [177071] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90083191 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.4: Street and highway 1,708 European ancestry cases, 386,222 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081102 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Financial situation satisfaction - Extremely unhappy (UKB data field 4581) (Gene-based burden) 2,657 European ancestry cases, 174,166 European ancestry controls NA Illumina [177071] 0 financial situation satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009726 GCST90083196 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W01.9: Unspecified place 2,111 European ancestry cases, 385,819 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081104 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N03: Chronic nephritic syndrome 978 European ancestry cases, 386,890 European ancestry controls NA Affymetrix, Illumina [510637] 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90080573 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C85: Other specified and unspecified types of non-Hodgkin lymphoma (Gene-based burden) 1,579 European ancestry cases, 386,126 European ancestry controls NA Illumina [185340] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90083624 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.2: Esophageal obstruction 2,458 European ancestry cases, 385,407 European ancestry controls NA Affymetrix, Illumina [510636] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90080190 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C85.1: Unspecified B-cell lymphoma (Gene-based burden) 521 European ancestry cases, 387,409 European ancestry controls NA Illumina [185344] 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90083622 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92.1: Melena 3,226 European ancestry cases, 384,649 European ancestry controls NA Affymetrix, Illumina [510636] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080320 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C85.9: Non-Hodgkin lymphoma, unspecified (Gene-based burden) 1,233 European ancestry cases, 386,688 European ancestry controls NA Illumina [185344] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90083623 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77: Secondary and unspecified malignant neoplasm of lymph nodes 7,019 European ancestry cases, 380,863 European ancestry controls 596 European ancestry cases, 121,325 European ancestry controls Affymetrix, Illumina [510635] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079620 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C90: Multiple myeloma and malignant plasma cell neoplasms (Gene-based burden) 772 European ancestry cases, 387,101 European ancestry controls NA Illumina [185343] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90083626 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R18: Ascites 2,103 European ancestry cases, 385,762 European ancestry controls NA Affymetrix, Illumina [510635] 0 Ascites http://purl.obolibrary.org/obo/HP_0001541 GCST90080807 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C90.0: Multiple myeloma (Gene-based burden) 739 European ancestry cases, 387,155 European ancestry controls NA Illumina [185343] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90083625 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I51.9: Heart disease, unspecified 909 European ancestry cases, 386,964 European ancestry controls NA Affymetrix, Illumina [510634] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90080026 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C91: Lymphoid leukemia (Gene-based burden) 878 European ancestry cases, 386,951 European ancestry controls NA Illumina [185327] 0 lymphoid leukemia http://www.ebi.ac.uk/efo/EFO_0004289 GCST90083628 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34: Malignant neoplasm of bronchus and lung 3,122 European ancestry cases, 384,752 European ancestry controls NA Affymetrix, Illumina [510633] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90079590 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C91.1: Chronic lymphocytic leukemia of B-cell type (Gene-based burden) 669 European ancestry cases, 387,257 European ancestry controls NA Illumina [185344] 0 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90083627 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D11: Benign neoplasm of major salivary glands 567 European ancestry cases, 387,293 European ancestry controls NA Affymetrix, Illumina [510633] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079653 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C92: Myeloid leukemia (Gene-based burden) 572 European ancestry cases, 387,341 European ancestry controls NA Illumina [185330] 0 myeloid neoplasm http://www.ebi.ac.uk/efo/EFO_0002427 GCST90083629 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.50: Unspecified fracture of pubis 578 European ancestry cases, 387,277 European ancestry controls NA Affymetrix, Illumina [510630] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080968 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D03: Melanoma in situ (Gene-based burden) 969 European ancestry cases, 386,791 European ancestry controls NA Illumina [185341] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083630 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z03.5: Observation for other suspected cardiovascular diseases 1,523 European ancestry cases, 386,346 European ancestry controls NA Affymetrix, Illumina [510630] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081190 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D04: Carcinoma in situ of skin (Gene-based burden) 973 European ancestry cases, 386,773 European ancestry controls NA Illumina [185341] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083631 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95.6: Staphylococcus aureus as the cause of diseases classified elsewhere 2,837 European ancestry cases, 385,030 European ancestry controls NA Affymetrix, Illumina [510629] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079562 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D05: Carcinoma in situ of breast (Gene-based burden) 2,611 European ancestry cases, 209,012 European ancestry controls NA Illumina [179918] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90083634 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31.9: Disease of stomach and duodenum, unspecified 883 European ancestry cases, 386,985 European ancestry controls NA Affymetrix, Illumina [510629] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90080212 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D05.1: Intraductal carcinoma in situ of breast (Gene-based burden) 1,447 European ancestry cases, 227,687 European ancestry controls NA Illumina [180826] 0 intraductal breast neoplasm http://purl.obolibrary.org/obo/MONDO_0002488 GCST90083632 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D32: Benign neoplasm of meninges 651 European ancestry cases, 387,220 European ancestry controls NA Affymetrix, Illumina [510628] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079692 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hayfever, allergic rhinitis or eczema (UKB data field 6152) (Gene-based burden) 101,576 European ancestry cases, 39,385 European ancestry controls NA Illumina [172802] 0 seasonal allergic rhinitis, Eczema http://www.ebi.ac.uk/efo/EFO_0003956, http://purl.obolibrary.org/obo/HP_0000964 GCST90083443 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glycated haemoglobin HbA1c levels (UKB data field 30750) 412,234 European ancestry individuals 68,967 European ancestry individuals Affymetrix, Illumina [532206] 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90079030 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg deep vein thrombosis (UKB data field 6152) (Gene-based burden) 9,223 European ancestry cases, 131,738 European ancestry controls NA Illumina [172802] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90083439 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alanine aminotransferase levels (UKB data field 30620) 411,932 European ancestry individuals 109,909 European ancestry individuals Affymetrix, Illumina [532198] 2 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90079014 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bronchiectasis (UKB data field 22134) (Gene-based burden) 947 European ancestry cases, 107,302 European ancestry controls NA Illumina [166035] 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90082851 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Creatinine levels (UKB data field 30700) 411,881 European ancestry individuals 115,985 European ancestry individuals Affymetrix, Illumina [532181] 2 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90079025 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cancer (UKB data field 2453) (Gene-based burden) 36,403 European ancestry cases, 393,153 European ancestry controls NA Illumina [185932] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90082936 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Gamma glutamyltransferase levels (UKB data field 30730) 411,861 European ancestry individuals 7,238 European ancestry individuals Affymetrix, Illumina [532147] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90079028 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic bronchitis (UKB data field 22129) (Gene-based burden) 1,225 European ancestry cases, 107,024 European ancestry controls NA Illumina [166035] 0 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST90082849 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urea levels (UKB data field 30670) 411,808 European ancestry individuals 116,216 European ancestry individuals Affymetrix, Illumina [532124] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90079022 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease (UKB data field 22130) (Gene-based burden) 1,566 European ancestry cases, 106,683 European ancestry controls NA Illumina [166035] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90082850 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Triglyceride levels (UKB data field 30870) 411,757 European ancestry individuals 93,219 European ancestry individuals Affymetrix, Illumina [532067] 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90079044 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetes mellitus (UKB data field 2443) (Gene-based burden) 22,058 European ancestry cases, 407,681 European ancestry controls NA Illumina [185922] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90082935 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Urate levels (UKB data field 30880) 411,604 European ancestry individuals 26,348 European ancestry individuals Affymetrix, Illumina [531905] 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90079045 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hayfever or rhinitis (UKB data field 22126) (Gene-based burden) 24,550 European ancestry cases, 83,699 European ancestry controls NA Illumina [166035] 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST90082847 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Direct low density lipoprotein levels (UKB data field 30780) 411,351 European ancestry individuals 92,395 European ancestry individuals Affymetrix, Illumina [531723] 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90079033 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tuberculosis (UKB data field 22137) (Gene-based burden) 574 European ancestry cases, 107,675 European ancestry controls NA Illumina [166035] 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90082852 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. C reactive protein levels (UKB data field 30710) 411,229 European ancestry individuals 21,098 European ancestry individuals Affymetrix, Illumina [531587] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90079026 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Angina (UKB data field 6150) (Gene-based burden) 14,103 European ancestry cases, 115,540 European ancestry controls NA Illumina [170818] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90083429 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Aspartate aminotransferase levels (UKB data field 30650) 410,630 European ancestry individuals 108,635 European ancestry individuals Affymetrix, Illumina [531161] 2 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90079020 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Heart attack (UKB data field 6150) (Gene-based burden) 10,286 European ancestry cases, 119,357 European ancestry controls NA Illumina [170818] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90083428 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Possible type 2 diabetes 2,316 European ancestry cases, 408,623 European ancestry controls NA Affymetrix, Illumina [531156] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90081524 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High blood pressure (UKB data field 6150) (Gene-based burden) 117,747 European ancestry cases, 11,896 European ancestry controls NA Illumina [170818] 0 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90083431 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Total bilirubin levels (UKB data field 30840) 410,431 European ancestry individuals 108,358 European ancestry individuals Affymetrix, Illumina [530989] 6 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90079041 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stroke (UKB data field 6150) (Gene-based burden) 6,774 European ancestry cases, 122,869 European ancestry controls NA Illumina [170818] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90083430 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.3: Other and unspecified malignant neoplasm of skin of other and unspecified parts of face (Gene-based burden) 7,572 European ancestry cases, 380,358 European ancestry controls NA Illumina [185344] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083582 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50.0: Cervical disc disorder with myelopathy 505 European ancestry cases, 387,385 European ancestry controls NA Affymetrix, Illumina [510657] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90080491 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.4: Other and unspecified malignant neoplasm of skin of scalp and neck (Gene-based burden) 1,835 European ancestry cases, 386,072 European ancestry controls NA Illumina [185344] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083583 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T82: Complications of cardiac and vascular prosthetic devices, implants and grafts 3,110 European ancestry cases, 384,779 European ancestry controls NA Affymetrix, Illumina [510657] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081075 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.5: Other and unspecified malignant neoplasm of skin of trunk (Gene-based burden) 2,526 European ancestry cases, 385,397 European ancestry controls NA Illumina [185344] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083584 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C15: Malignant neoplasm of esophagus 992 European ancestry cases, 386,907 European ancestry controls NA Affymetrix, Illumina [510656] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90079575 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.6: Other and unspecified malignant neoplasm of skin of upper limb, including shoulder (Gene-based burden) 1,542 European ancestry cases, 386,385 European ancestry controls NA Illumina [185344] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083585 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55: Nerve root and plexus compressions in diseases classified elsewhere 5,243 European ancestry cases, 382,644 European ancestry controls NA Affymetrix, Illumina [510656] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90079843 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.7: Other and unspecified malignant neoplasm of skin of lower limb, including hip (Gene-based burden) 1,262 European ancestry cases, 386,666 European ancestry controls NA Illumina [185344] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083586 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72.1: Pertrochanteric fracture 535 European ancestry cases, 387,361 European ancestry controls NA Affymetrix, Illumina [510656] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081012 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50: Malignant neoplasm of breast (Gene-based burden) 12,346 European ancestry cases, 198,242 European ancestry controls NA Illumina [179866] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90083592 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z48: Encounter for other postprocedural aftercare 1,761 European ancestry cases, 386,128 European ancestry controls NA Affymetrix, Illumina [510656] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081271 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.2: Malignant neoplasm of upper-inner quadrant of breast (Gene-based burden) 775 European ancestry cases, 228,359 European ancestry controls NA Illumina [180826] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083588 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H65.3: Chronic mucoid otitis media 732 European ancestry cases, 387,162 European ancestry controls NA Affymetrix, Illumina [510655] 0 chronic otitis media http://purl.obolibrary.org/obo/MONDO_0021204 GCST90079931 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.4: Malignant neoplasm of upper-outer quadrant of breast (Gene-based burden) 2,461 European ancestry cases, 226,673 European ancestry controls NA Illumina [180826] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083589 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I74.3: Embolism and thrombosis of arteries of the lower extremities 686 European ancestry cases, 387,213 European ancestry controls NA Affymetrix, Illumina [510655] 0 arterial embolism, Arterial thrombosis http://www.ebi.ac.uk/efo/EFO_0010671, http://purl.obolibrary.org/obo/HP_0004420 GCST90080052 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.8: Malignant neoplasm of overlapping sites of breast (Gene-based burden) 600 European ancestry cases, 228,534 European ancestry controls NA Illumina [180826] 0 breast neoplasm http://www.ebi.ac.uk/efo/EFO_0003869 GCST90083590 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92.0: Hematemesis 2,304 European ancestry cases, 385,588 European ancestry controls NA Affymetrix, Illumina [510655] 0 Hematemesis http://purl.obolibrary.org/obo/HP_0002248 GCST90080319 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C50.9: Malignant neoplasm of breast of unspecified site (Gene-based burden) 8,909 European ancestry cases, 202,443 European ancestry controls NA Illumina [179894] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90083591 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I62: Other and unspecified nontraumatic intracranial hemorrhage 590 European ancestry cases, 387,284 European ancestry controls NA Affymetrix, Illumina [510654] 0 intracranial hemorrhage http://www.ebi.ac.uk/efo/EFO_0000551 GCST90080032 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C54: Malignant neoplasm of corpus uteri (Gene-based burden) 1,515 European ancestry cases, 210,164 European ancestry controls NA Illumina [179929] 0 uterine corpus cancer http://www.ebi.ac.uk/efo/EFO_0007532 GCST90083594 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.9: Rheumatoid arthritis, unspecified 5,220 European ancestry cases, 382,668 European ancestry controls NA Affymetrix, Illumina [510654] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90080391 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C54.1: Malignant neoplasm of endometrium (Gene-based burden) 1,469 European ancestry cases, 227,317 European ancestry controls NA Illumina [180818] 0 endometrial cancer http://purl.obolibrary.org/obo/MONDO_0011962 GCST90083593 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85.5: Personal history of malignant neoplasm of urinary tract 3,617 European ancestry cases, 384,280 European ancestry controls NA Affymetrix, Illumina [510654] 0 Malignant Urinary System Neoplasm http://www.ebi.ac.uk/efo/EFO_1000363 GCST90081351 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C56: Malignant neoplasm of ovary (Gene-based burden) 1,188 European ancestry cases, 210,464 European ancestry controls NA Illumina [179926] 0 ovarian neoplasm http://www.ebi.ac.uk/efo/EFO_0003893 GCST90083595 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cerebrovascular disease - ischemic composite (Gene-based burden) 9,143 European ancestry cases, 371,403 European ancestry controls NA Illumina [185201] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90085456 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 503 Most of the time (UKB data field 21028) (Gene-based burden) 22,017 European ancestry cases, 61,084 European ancestry controls NA Illumina [159594] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082686 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.0: Follow-up examination after surgery for other conditions 5,895 European ancestry cases, 382,035 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081201 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain getting better or stopping after a bowel movement - 504 Always (UKB data field 21028) (Gene-based burden) 16,102 European ancestry cases, 66,999 European ancestry controls NA Illumina [159594] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082687 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.2: Follow-up examination after chemotherapy for other conditions 1,891 European ancestry cases, 386,039 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081202 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Every day (UKB data field 21025) (Gene-based burden) 3,727 European ancestry cases, 151,293 European ancestry controls NA Illumina [174055] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082680 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.8: Follow-up examination after other treatment for other conditions 3,238 European ancestry cases, 384,692 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081203 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Less than one day a month (UKB data field 21025) (Gene-based burden) 30,431 European ancestry cases, 124,589 European ancestry controls NA Illumina [174055] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082675 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09.9: Follow-up examination after unspecified treatment for other conditions 3,011 European ancestry cases, 384,919 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081204 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34.3: Malignant neoplasm of lower lobe, bronchus or lung (Gene-based burden) 695 European ancestry cases, 387,235 European ancestry controls NA Illumina [185344] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90083574 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.9: Liver disease, unspecified 928 European ancestry cases, 386,964 European ancestry controls NA Affymetrix, Illumina [510660] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90080291 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34.9: Malignant neoplasm of unspecified part of bronchus or lung (Gene-based burden) 2,548 European ancestry cases, 385,381 European ancestry controls NA Illumina [185344] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90083575 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.2: Calculus of gallbladder without cholecystitis 10,288 European ancestry cases, 377,616 European ancestry controls 6,041 European ancestry cases, 108,108 European ancestry controls Affymetrix, Illumina [510660] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90080295 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C43: Malignant melanoma of skin (Gene-based burden) 2,807 European ancestry cases, 384,475 European ancestry controls NA Illumina [185331] 0 cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0000389 GCST90083579 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.5: Other deformities of toe(s) (acquired) 2,079 European ancestry cases, 385,807 European ancestry controls NA Affymetrix, Illumina [510660] 0 Abnormal foot morphology http://purl.obolibrary.org/obo/HP_0001760 GCST90080431 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C43.6: Malignant melanoma of upper limb, including shoulder (Gene-based burden) 614 European ancestry cases, 387,316 European ancestry controls NA Illumina [185344] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083577 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z94: Transplanted organ and tissue status 1,305 European ancestry cases, 386,601 European ancestry controls 1,087 European ancestry cases, 34,876 European ancestry controls Affymetrix, Illumina [510660] 0 transplant outcome measurement http://www.ebi.ac.uk/efo/EFO_0005198 GCST90081418 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C43.7: Malignant melanoma of lower limb, including hip (Gene-based burden) 793 European ancestry cases, 387,137 European ancestry controls NA Illumina [19298] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083578 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G91: Hydrocephalus 595 European ancestry cases, 387,290 European ancestry controls NA Affymetrix, Illumina [510659] 0 Hydrocephalus http://purl.obolibrary.org/obo/HP_0000238 GCST90079856 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44: Other and unspecified malignant neoplasm of skin (Gene-based burden) 15,858 European ancestry cases, 368,260 European ancestry controls NA Illumina [185269] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083587 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F05: Delirium due to known physiological condition 1,350 European ancestry cases, 386,554 European ancestry controls NA Affymetrix, Illumina [510658] 0 alcohol withdrawal delirium http://www.ebi.ac.uk/efo/EFO_1000800 GCST90079786 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.1: Other and unspecified malignant neoplasm of skin of eyelid, including canthus (Gene-based burden) 1,565 European ancestry cases, 386,363 European ancestry controls NA Illumina [185344] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083580 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.8: Other specified disorders of bladder 7,761 European ancestry cases, 380,142 European ancestry controls NA Affymetrix, Illumina [510658] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90080605 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.2: Other and unspecified malignant neoplasm of skin of ear and external auricular canal (Gene-based burden) 1,075 European ancestry cases, 386,855 European ancestry controls NA Illumina [185344] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083581 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31.8: Other specified diseases of stomach and duodenum 3,075 European ancestry cases, 384,823 European ancestry controls NA Affymetrix, Illumina [510657] 0 stomach disease http://www.ebi.ac.uk/efo/EFO_0009608 GCST90080211 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.0: Secondary malignant neoplasm of lung (Gene-based burden) 2,742 European ancestry cases, 385,188 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083607 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I95.9: Hypotension, unspecified 5,127 European ancestry cases, 382,771 European ancestry controls NA Affymetrix, Illumina [510646] 0 hypotension http://www.ebi.ac.uk/efo/EFO_0005251 GCST90080082 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed mood in last 2 weeks - Several days (UKB data field 2050) 81,404 European ancestry cases, 332,165 European ancestry controls NA Affymetrix, Illumina [533338] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078574 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cerebrovascular disease - ischemic composite (no atrial fibrillation) (Gene-based burden) 6,889 European ancestry cases, 353,545 European ancestry controls NA Illumina [184858] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90085457 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Irritability (UKB data field 1940) 120,504 European ancestry cases, 292,618 European ancestry controls NA Affymetrix, Illumina [532927] 0 Irritability http://purl.obolibrary.org/obo/HP_0000737 GCST90077620 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - Cylindrical power left (UKB data field 5086) (Gene-based burden) 107,117 European ancestry individuals NA Illumina [167449] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083255 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reticulocyte count (UKB data field 30250) 412,501 European ancestry individuals 7,696 European ancestry individuals Affymetrix, Illumina [532687] 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90079001 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - Cylindrical power right (UKB data field 5087) (Gene-based burden) 107,475 European ancestry individuals NA Illumina [167589] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90083256 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean reticulocyte volume (UKB data field 30260) 412,501 European ancestry individuals NA Affymetrix, Illumina [532686] 12 mean reticulocyte volume http://www.ebi.ac.uk/efo/EFO_0010701 GCST90079002 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cystatin C levels (UKB data field 30720) (Gene-based burden) 412,047 European ancestry individuals NA Illumina [185666] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90083013 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reticulocyte percentage (UKB data field 30240) 412,501 European ancestry individuals 7,696 European ancestry individuals Affymetrix, Illumina [532686] 0 reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0010700 GCST90079000 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Daytime dozing sleeping narcolepsy - Never rarely (UKB data field 1220) (Gene-based burden) 333,750 European ancestry cases, 95,395 European ancestry controls NA Illumina [185913] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90081567 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High light scatter reticulocyte count (UKB data field 30300) 412,333 European ancestry individuals NA Affymetrix, Illumina [532548] 17 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90079006 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Daytime dozing sleeping narcolepsy - Often (UKB data field 1220) (Gene-based burden) 12,346 European ancestry cases, 416,799 European ancestry controls NA Illumina [185913] 0 narcolepsy without cataplexy, excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0005855, http://www.ebi.ac.uk/efo/EFO_0007875 GCST90081569 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High light scatter reticulocyte percentage (UKB data field 30290) 412,334 European ancestry individuals NA Affymetrix, Illumina [532548] 14 reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0010700 GCST90079005 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Daytime dozing sleeping narcolepsy - Sometimes (UKB data field 1220) (Gene-based burden) 94,586 European ancestry cases, 334,559 European ancestry controls NA Illumina [185913] 0 narcolepsy without cataplexy, excessive daytime sleepiness measurement http://www.ebi.ac.uk/efo/EFO_0005855, http://www.ebi.ac.uk/efo/EFO_0007875 GCST90081568 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Mean sphered cell volume (UKB data field 30270) 412,334 European ancestry individuals NA Affymetrix, Illumina [532548] 12 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90079003 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma (UKB data field 22127) (Gene-based burden) 13,735 European ancestry cases, 94,514 European ancestry controls NA Illumina [166035] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90082848 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Immature reticulocyte fraction (UKB data field 30280) 412,333 European ancestry individuals NA Affymetrix, Illumina [532547] 6 reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0010700 GCST90079004 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Asthma (UKB data field 6152) (Gene-based burden) 50,805 European ancestry cases, 90,156 European ancestry controls NA Illumina [172802] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90083442 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cholesterol levels (UKB data field 30690) 412,075 European ancestry individuals 92,936 European ancestry individuals Affymetrix, Illumina [532346] 4 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90079024 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Blood clot in the lung (UKB data field 6152) (Gene-based burden) 3,718 European ancestry cases, 137,243 European ancestry controls NA Illumina [172802] 0 Abnormal thrombosis http://purl.obolibrary.org/obo/HP_0001977 GCST90083441 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Alkaline phosphatase levels (UKB data field 30610) 412,086 European ancestry individuals 108,268 European ancestry individuals Affymetrix, Illumina [532338] 5 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90079013 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic obstructive pulmonary disease (UKB data field 6152) (Gene-based burden) 7,705 European ancestry cases, 133,256 European ancestry controls NA Illumina [172802] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90083440 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cystatin C levels (UKB data field 30720) 412,047 European ancestry individuals NA Affymetrix, Illumina [532315] 8 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90079027 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H34.8: Other retinal vascular occlusions 539 European ancestry cases, 387,344 European ancestry controls NA Affymetrix, Illumina [510653] 0 retinal vein occlusion http://www.ebi.ac.uk/efo/EFO_1001157 GCST90079898 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C64: Malignant neoplasm of kidney, except renal pelvis (Gene-based burden) 1,355 European ancestry cases, 386,525 European ancestry controls NA Illumina [185344] 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90083596 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Q21.1: Atrial septal defect 554 European ancestry cases, 387,345 European ancestry controls NA Affymetrix, Illumina [510653] 0 atrial heart septal defect http://www.ebi.ac.uk/efo/EFO_1000825 GCST90080747 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C67: Malignant neoplasm of bladder (Gene-based burden) 2,670 European ancestry cases, 385,138 European ancestry controls NA Illumina [185342] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90083598 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I31.9: Disease of pericardium, unspecified 578 European ancestry cases, 387,309 European ancestry controls NA Affymetrix, Illumina [510652] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90079989 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C67.9: Malignant neoplasm of bladder, unspecified (Gene-based burden) 2,407 European ancestry cases, 385,519 European ancestry controls NA Illumina [185344] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90083597 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93.2: Ileostomy status 1,429 European ancestry cases, 386,458 European ancestry controls 434 European ancestry cases, 34,847 European ancestry controls Affymetrix, Illumina [510652] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081413 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C71: Malignant neoplasm of brain (Gene-based burden) 678 European ancestry cases, 387,224 European ancestry controls NA Illumina [185344] 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90083600 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.5: Encounter for palliative care 5,496 European ancestry cases, 382,396 European ancestry controls 2,064 European ancestry cases, 97,679 European ancestry controls Affymetrix, Illumina [510651] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081283 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C71.9: Malignant neoplasm of brain, unspecified (Gene-based burden) 550 European ancestry cases, 387,380 European ancestry controls NA Illumina [185344] 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90083599 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D63.165.8: Anemia in chronic kidney disease 936 European ancestry cases, 386,949 European ancestry controls NA Affymetrix, Illumina [510648] 1 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90079710 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77: Secondary and unspecified malignant neoplasm of lymph nodes (Gene-based burden) 7,019 European ancestry cases, 380,863 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083606 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I85.9: Oesophageal varices without bleeding 643 European ancestry cases, 387,287 European ancestry controls NA Affymetrix, Illumina [510648] 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90080075 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.0: Secondary and unspecified malignant neoplasm of lymph nodes of head, face and neck (Gene-based burden) 933 European ancestry cases, 386,997 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083601 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.8: Candidiasis of other sites 1,130 European ancestry cases, 386,725 European ancestry controls NA Affymetrix, Illumina [510647] 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90079559 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.1: Secondary and unspecified malignant neoplasm of intrathoracic lymph nodes (Gene-based burden) 1,267 European ancestry cases, 386,663 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083602 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44.2: Atrioventricular block, complete 841 European ancestry cases, 387,048 European ancestry controls NA Affymetrix, Illumina [510647] 0 atrioventricular block http://purl.obolibrary.org/obo/MONDO_0000465 GCST90080003 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.2: Secondary and unspecified malignant neoplasm of intra-abdominal lymph nodes (Gene-based burden) 1,880 European ancestry cases, 386,050 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083603 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J69: Pneumonitis due to solids and liquids 1,140 European ancestry cases, 386,749 European ancestry controls NA Affymetrix, Illumina [510647] 0 pneumonitis http://www.ebi.ac.uk/efo/EFO_1001991 GCST90080144 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.3: Secondary and unspecified malignant neoplasm of axilla and upper limb lymph nodes (Gene-based burden) 2,725 European ancestry cases, 385,205 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083604 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K72: Hepatic failure, not elsewhere classified 566 European ancestry cases, 387,314 European ancestry controls NA Affymetrix, Illumina [510647] 0 Hepatic failure http://purl.obolibrary.org/obo/HP_0001399 GCST90080284 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.9: Secondary and unspecified malignant neoplasm of lymph node, unspecified (Gene-based burden) 650 European ancestry cases, 387,279 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083605 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.20: Derangement of unspecified meniscus due to old tear or injury 1,283 European ancestry cases, 386,609 European ancestry controls NA Affymetrix, Illumina [510647] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080434 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78: Secondary malignant neoplasm of respiratory and digestive organs (Gene-based burden) 6,526 European ancestry cases, 381,309 European ancestry controls NA Illumina [185342] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083611 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C92: Myeloid leukemia 572 European ancestry cases, 387,341 European ancestry controls 207 European ancestry cases, 122,669 European ancestry controls Affymetrix, Illumina [510646] 3 myeloid neoplasm http://www.ebi.ac.uk/efo/EFO_0002427 GCST90079643 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.2: Secondary malignant neoplasm of pleura (Gene-based burden) 815 European ancestry cases, 387,115 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083608 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I61.9: Nontraumatic intracerebral hemorrhage, unspecified 698 European ancestry cases, 387,165 European ancestry controls NA Affymetrix, Illumina [510645] 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90080030 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.6: Secondary malignant neoplasm of retroperitoneum and peritoneum (Gene-based burden) 1,833 European ancestry cases, 386,097 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083609 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I65.2: Occlusion and stenosis of carotid artery 1,229 European ancestry cases, 386,700 European ancestry controls NA Affymetrix, Illumina [510645] 0 carotid artery thrombosis http://www.ebi.ac.uk/efo/EFO_1000853 GCST90080037 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.7: Secondary malignant neoplasm of liver and intrahepatic bile duct (Gene-based burden) 3,748 European ancestry cases, 384,182 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083610 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E10.3: Type 1 diabetes mellitus with ophthalmic complications 587 European ancestry cases, 387,305 European ancestry controls NA Affymetrix, Illumina [510644] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90079731 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79: Secondary malignant neoplasm of other and unspecified sites (Gene-based burden) 5,376 European ancestry cases, 382,352 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083615 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20.9: Angina pectoris, unspecified 18,859 European ancestry cases, 369,024 European ancestry controls 3,323 European ancestry cases, 104,775 European ancestry controls Affymetrix, Illumina [510643] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90079967 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79.3: Secondary malignant neoplasm of brain and cerebral meninges (Gene-based burden) 1,145 European ancestry cases, 386,785 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083612 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.2: Escherichia coli [E. coli ] as the cause of diseases classified elsewhere 3,844 European ancestry cases, 384,028 European ancestry controls NA Affymetrix, Illumina [510641] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079566 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79.5: Secondary malignant neoplasm of bone and bone marrow (Gene-based burden) 3,104 European ancestry cases, 384,826 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083613 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C90: Multiple myeloma and malignant plasma cell neoplasms 772 European ancestry cases, 387,101 European ancestry controls NA Affymetrix, Illumina [510641] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90079640 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79.8: Secondary malignant neoplasm of other specified sites (Gene-based burden) 1,374 European ancestry cases, 386,553 European ancestry controls NA Illumina [185344] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90083614 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W25: Contact with sharp glass 610 European ancestry cases, 387,268 European ancestry controls NA Affymetrix, Illumina [510641] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081123 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C80: Malignant neoplasm without specification of site (Gene-based burden) 2,342 European ancestry cases, 384,910 European ancestry controls NA Illumina [185340] 0 GCST90083618 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S52.00: Unspecified fracture of upper end of ulna 758 European ancestry cases, 387,122 European ancestry controls NA Affymetrix, Illumina [510640] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080984 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C80.0: Disseminated malignant neoplasm, unspecified (Gene-based burden) 570 European ancestry cases, 387,360 European ancestry controls NA Illumina [185344] 0 GCST90083616 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z57: Occupational exposure to risk factors 734 European ancestry cases, 387,125 European ancestry controls NA Affymetrix, Illumina [510640] 0 risk factor http://www.ebi.ac.uk/efo/EFO_0003919 GCST90081297 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C80.9: Malignant neoplasm, unspecified (Gene-based burden) 572 European ancestry cases, 387,358 European ancestry controls NA Illumina [185344] 0 GCST90083617 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C64: Malignant neoplasm of kidney, except renal pelvis 1,355 European ancestry cases, 386,525 European ancestry controls NA Affymetrix, Illumina [510639] 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90079610 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C82: Follicular lymphoma (Gene-based burden) 538 European ancestry cases, 387,366 European ancestry controls NA Illumina [185339] 0 follicular lymphoma http://purl.obolibrary.org/obo/MONDO_0018906 GCST90083619 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83.1: Varicose veins of lower extremities with inflammation 594 European ancestry cases, 387,285 European ancestry controls NA Affymetrix, Illumina [510638] 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90080064 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C83: Non-follicular lymphoma (Gene-based burden) 1,109 European ancestry cases, 386,801 European ancestry controls NA Illumina [185344] 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90083621 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z29: Encounter for other prophylactic measures 916 European ancestry cases, 386,945 European ancestry controls NA Affymetrix, Illumina [510638] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081229 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C83.3: Diffuse large B-cell lymphoma (Gene-based burden) 768 European ancestry cases, 387,162 European ancestry controls NA Illumina [185344] 0 diffuse large B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000403 GCST90083620 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diastolic blood pressure automated reading (UKB data field 4079) 408,215 European ancestry individuals 121,665 European ancestry individuals Affymetrix, Illumina [530785] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90079145 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by back pain in the past three months - 600 Not bothered at all (UKB data field 21048) (Gene-based burden) 60,787 European ancestry cases, 94,352 European ancestry controls NA Illumina [174060] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082771 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pulse rate automated reading (UKB data field 102) 408,215 European ancestry individuals 121,418 European ancestry individuals Affymetrix, Illumina [530785] 1 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90077560 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by back pain in the past three months - 601 Bothered a little (UKB data field 21048) (Gene-based burden) 72,655 European ancestry cases, 82,484 European ancestry controls NA Illumina [174060] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082772 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Systolic blood pressure automated reading (UKB data field 4080) 408,211 European ancestry individuals 121,966 European ancestry individuals Affymetrix, Illumina [530783] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90079146 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by back pain in the past three months - 602 Bothered a lot (UKB data field 21048) (Gene-based burden) 21,697 European ancestry cases, 133,442 European ancestry controls NA Illumina [174060] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082773 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Apolipoprotein B levels (UKB data field 30640) 410,113 European ancestry individuals NA Affymetrix, Illumina [530598] 9 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90079018 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by chest pain in the last three months - 600 Not bothered at all (UKB data field 21052) (Gene-based burden) 133,883 European ancestry cases, 21,225 European ancestry controls NA Illumina [174057] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082783 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. IGF 1 (UKB data field 30770) 409,926 European ancestry individuals NA Affymetrix, Illumina [530454] 9 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90079032 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by chest pain in the last three months - 601 Bothered a little (UKB data field 21052) (Gene-based burden) 19,597 European ancestry cases, 135,511 European ancestry controls NA Illumina [174057] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082784 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Probable type 1 diabetes 1,290 European ancestry cases, 408,623 European ancestry controls NA Affymetrix, Illumina [530213] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90081525 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by chest pain in the last three months - 602 Bothered a lot (UKB data field 21052) (Gene-based burden) 1,628 European ancestry cases, 153,480 European ancestry controls NA Illumina [174057] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082785 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - More than one day a week (UKB data field 21025) (Gene-based burden) 13,542 European ancestry cases, 141,478 European ancestry controls NA Illumina [174055] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082679 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z42: Encounter for plastic and reconstructive surgery following medical procedure or healed injury 2,861 European ancestry cases, 385,069 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081258 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Never (UKB data field 21025) (Gene-based burden) 71,454 European ancestry cases, 83,566 European ancestry controls NA Illumina [174055] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082674 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z42.1: Encounter for breast reconstruction following mastectomy 2,185 European ancestry cases, 385,745 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081257 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - One day a month (UKB data field 21025) (Gene-based burden) 10,030 European ancestry cases, 144,990 European ancestry controls NA Illumina [174055] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082676 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z43.2: Encounter for attention to ileostomy 1,010 European ancestry cases, 386,920 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081259 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - One day a week (UKB data field 21025) (Gene-based burden) 5,396 European ancestry cases, 149,624 European ancestry controls NA Illumina [174055] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082678 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45.2: Encounter for adjustment and management of vascular access device 1,644 European ancestry cases, 386,286 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90081262 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of discomfort pain in abdomen in last three months - Two to three days a month (UKB data field 21025) (Gene-based burden) 20,440 European ancestry cases, 134,580 European ancestry controls NA Illumina [174055] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90082677 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z45.8: Encounter for adjustment and management of other implanted devices 1,272 European ancestry cases, 386,658 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service for adjustment and management of implanted device http://www.ebi.ac.uk/efo/EFO_0020982 GCST90081263 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - Monthly or less (UKB data field 20414) (Gene-based burden) 17,982 European ancestry cases, 121,560 European ancestry controls NA Illumina [172128] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082413 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z46: Encounter for fitting and adjustment of other devices 6,157 European ancestry cases, 381,771 European ancestry controls 1,095 European ancestry cases, 105,489 European ancestry controls Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081266 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - Never (UKB data field 20414) (Gene-based burden) 11,380 European ancestry cases, 128,162 European ancestry controls NA Illumina [172128] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082412 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - Nearly every day (UKB data field 2060) 8,385 European ancestry cases, 409,082 European ancestry controls NA Affymetrix, Illumina [536502] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078674 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm left - started wearing glasses or contacts before 40 (Gene-based burden) 47,125 European ancestry individuals NA Illumina [142420] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085465 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - Not at all (UKB data field 2060) 335,869 European ancestry cases, 81,598 European ancestry controls NA Affymetrix, Illumina [536502] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078671 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm right (Gene-based burden) 103,540 European ancestry individuals NA Illumina [166614] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085466 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of unenthusiasm disinterest in last 2 weeks - Several days (UKB data field 2060) 71,590 European ancestry cases, 345,877 European ancestry controls NA Affymetrix, Illumina [536502] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078672 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm right - started wearing glasses or contacts before 40 (Gene-based burden) 47,122 European ancestry individuals NA Illumina [142404] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085467 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Risk taking (UKB data field 2040) 113,078 European ancestry cases, 303,726 European ancestry controls NA Affymetrix, Illumina [535989] 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90078418 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm left (Gene-based burden) 89,735 European ancestry individuals NA Illumina [162980] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085468 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Suffer from nerves (UKB data field 2010) 91,369 European ancestry cases, 324,851 European ancestry controls NA Affymetrix, Illumina [535663] 0 feeling nervous measurement http://www.ebi.ac.uk/efo/EFO_0009597 GCST90078268 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 6mm right (Gene-based burden) 90,887 European ancestry individuals NA Illumina [163277] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90085469 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - More than half the days (UKB data field 2070) 11,135 European ancestry cases, 404,376 European ancestry controls NA Affymetrix, Illumina [534856] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078677 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cough on most days (UKB data field 22502) (Gene-based burden) 14,729 European ancestry cases, 93,520 European ancestry controls NA Illumina [166035] 0 Cough http://purl.obolibrary.org/obo/HP_0012735 GCST90082858 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - Nearly every day (UKB data field 2070) 7,849 European ancestry cases, 407,662 European ancestry controls NA Affymetrix, Illumina [534856] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078678 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Creatinine levels (UKB data field 30700) (Gene-based burden) 411,881 European ancestry individuals NA Illumina [185664] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90083011 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - Not at all (UKB data field 2070) 311,760 European ancestry cases, 103,751 European ancestry controls NA Affymetrix, Illumina [534856] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078675 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Creatinine enzymatic in urine (UKB data field 30510) (Gene-based burden) 419,176 European ancestry individuals NA Illumina [185813] 0 creatinine clearance measurement http://www.ebi.ac.uk/efo/EFO_0007934 GCST90082994 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of tenseness restlessness in last 2 weeks - Several days (UKB data field 2070) 96,739 European ancestry cases, 318,772 European ancestry controls NA Affymetrix, Illumina [534856] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078676 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Current eye infection (UKB data field 5183) (Gene-based burden) 1,271 European ancestry cases, 109,604 European ancestry controls NA Illumina [168390] 0 eye infectious disorder http://purl.obolibrary.org/obo/MONDO_0043885 GCST90083310 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing difficulty problems (UKB data field 2247) 114,857 European ancestry cases, 300,307 European ancestry controls NA Affymetrix, Illumina [534563] 4 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90078871 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Current tobacco smoking on most or all days (UKB data field 1239) (Gene-based burden) 33,523 European ancestry cases, 396,975 European ancestry controls NA Illumina [185942] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90081570 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Worry too long after embarrassment (UKB data field 2000) 203,159 European ancestry cases, 211,521 European ancestry controls NA Affymetrix, Illumina [534396] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078243 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Currently in last three months suffer from abdominal pain (UKB data field 21035) (Gene-based burden) 45,104 European ancestry cases, 109,755 European ancestry controls NA Illumina [174021] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082718 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed mood in last 2 weeks - More than half the days (UKB data field 2050) 12,239 European ancestry cases, 401,330 European ancestry controls NA Affymetrix, Illumina [533338] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078575 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Currently suffer from abdominal distension (UKB data field 21038) (Gene-based burden) 36,054 European ancestry cases, 118,772 European ancestry controls NA Illumina [174029] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082739 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed mood in last 2 weeks - Nearly every day (UKB data field 2050) 7,997 European ancestry cases, 405,572 European ancestry controls NA Affymetrix, Illumina [533338] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078576 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35: Other retinal disorders (Gene-based burden) 5,808 European ancestry cases, 378,620 European ancestry controls NA Illumina [185289] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90083888 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Liverp 6,098 European ancestry cases, 381,358 European ancestry controls NA Affymetrix, Illumina [510313] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90081521 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35.3: Degeneration of macula and posterior pole (Gene-based burden) 3,347 European ancestry cases, 384,583 European ancestry controls NA Illumina [185344] 0 degeneration of macula and posterior pole http://purl.obolibrary.org/obo/MONDO_0002175 GCST90083886 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N12: Tubulo-interstitial nephritis, not specified as acute or chronic 1,223 European ancestry cases, 386,282 European ancestry controls NA Affymetrix, Illumina [510303] 0 nephritis http://www.ebi.ac.uk/efo/EFO_1002050 GCST90080574 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35.8: Other specified retinal disorders (Gene-based burden) 1,101 European ancestry cases, 386,738 European ancestry controls NA Illumina [185344] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90083887 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K63.9: Disease of intestine, unspecified 1,019 European ancestry cases, 386,507 European ancestry controls NA Affymetrix, Illumina [510302] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080273 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H36: Retinal disorders in diseases classified elsewhere (Gene-based burden) 1,750 European ancestry cases, 386,178 European ancestry controls NA Illumina [185344] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90083890 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I26.9: Pulmonary embolism without acute cor pulmonale 5,096 European ancestry cases, 382,414 European ancestry controls 3,410 European ancestry cases, 117,976 European ancestry controls Affymetrix, Illumina [510299] 0 cor pulmonale http://purl.obolibrary.org/obo/MONDO_0004596 GCST90079983 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H36.0: Diabetic retinopathy (Gene-based burden) 1,748 European ancestry cases, 386,182 European ancestry controls NA Illumina [185344] 0 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST90083889 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D48: Neoplasm of uncertain behavior of other and unspecified sites 988 European ancestry cases, 386,500 European ancestry controls NA Affymetrix, Illumina [510298] 0 GCST90079700 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40: Glaucoma (Gene-based burden) 8,122 European ancestry cases, 376,438 European ancestry controls NA Illumina [185308] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90083895 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.0: Open wound of thumb without damage to nail 2,186 European ancestry cases, 385,319 European ancestry controls NA Affymetrix, Illumina [510297] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080993 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.0: Glaucoma suspect (Gene-based burden) 1,355 European ancestry cases, 386,553 European ancestry controls NA Illumina [185344] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90083891 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34.2: Deviated nasal septum 4,524 European ancestry cases, 382,965 European ancestry controls NA Affymetrix, Illumina [510296] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080114 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.1: Open-angle glaucoma (Gene-based burden) 1,520 European ancestry cases, 386,410 European ancestry controls NA Illumina [185344] 0 open-angle glaucoma http://www.ebi.ac.uk/efo/EFO_0004190 GCST90083892 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K51: Ulcerative colitis 3,928 European ancestry cases, 383,552 European ancestry controls NA Affymetrix, Illumina [510296] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90080234 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.2: Primary angle-closure glaucoma (Gene-based burden) 926 European ancestry cases, 387,004 European ancestry controls NA Illumina [185344] 0 primary angle closure glaucoma http://www.ebi.ac.uk/efo/EFO_1001506 GCST90083893 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z04: Encounter for examination and observation for other reasons 2,344 European ancestry cases, 385,137 European ancestry controls NA Affymetrix, Illumina [510294] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081196 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H40.9: Unspecified glaucoma (Gene-based burden) 3,672 European ancestry cases, 384,258 European ancestry controls NA Illumina [185344] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90083894 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D68: Other coagulation defects 1,286 European ancestry cases, 386,192 European ancestry controls NA Affymetrix, Illumina [510290] 0 blood coagulation disease http://www.ebi.ac.uk/efo/EFO_0009314 GCST90079713 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H43: Disorders of vitreous body (Gene-based burden) 3,002 European ancestry cases, 378,726 European ancestry controls NA Illumina [185231] 0 vitreous body disease http://www.ebi.ac.uk/efo/EFO_0008624 GCST90083898 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K35: Acute appendicitis 3,368 European ancestry cases, 384,092 European ancestry controls NA Affymetrix, Illumina [510285] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90080216 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H43.1: Vitreous hemorrhage (Gene-based burden) 620 European ancestry cases, 387,305 European ancestry controls NA Illumina [185340] 0 vitreous hemorrhage http://www.ebi.ac.uk/efo/EFO_0008626 GCST90083896 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Major bleeding 7,582 European ancestry cases, 379,910 European ancestry controls NA Affymetrix, Illumina [510282] 0 Abnormal bleeding http://purl.obolibrary.org/obo/HP_0001892 GCST90081532 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H43.8: Other disorders of vitreous body (Gene-based burden) 881 European ancestry cases, 387,028 European ancestry controls NA Illumina [185344] 0 vitreous body disease http://www.ebi.ac.uk/efo/EFO_0008624 GCST90083897 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.40: Fracture of malar, maxillary and zygoma bones, unspecified 505 European ancestry cases, 387,096 European ancestry controls NA Affymetrix, Illumina [510406] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080947 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H00: Hordeolum and chalazion (Gene-based burden) 4,139 European ancestry cases, 377,132 European ancestry controls NA Illumina [185241] 0 hordeolum, meibomian cyst http://www.ebi.ac.uk/efo/EFO_0007315, http://www.ebi.ac.uk/efo/EFO_0007363 GCST90083849 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.8: Other shoulder lesions 1,778 European ancestry cases, 385,821 European ancestry controls NA Affymetrix, Illumina [510404] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080536 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H00.1: Chalazion (Gene-based burden) 1,924 European ancestry cases, 386,006 European ancestry controls NA Illumina [185344] 0 meibomian cyst http://www.ebi.ac.uk/efo/EFO_0007363 GCST90083848 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.1: Rotator cuff tear or rupture, not specified as traumatic 4,628 European ancestry cases, 382,991 European ancestry controls NA Affymetrix, Illumina [510397] 0 rotator cuff tear http://www.ebi.ac.uk/efo/EFO_1001250 GCST90080533 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01: Other inflammation of eyelid (Gene-based burden) 2,724 European ancestry cases, 377,649 European ancestry controls NA Illumina [185211] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90083853 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S01.8: Open wound of other parts of head 1,527 European ancestry cases, 386,076 European ancestry controls NA Affymetrix, Illumina [510395] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080943 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01.0: Blepharitis (Gene-based burden) 1,881 European ancestry cases, 381,491 European ancestry controls NA Illumina [185271] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90083852 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W10: Fall on and from stairs and steps 3,736 European ancestry cases, 383,879 European ancestry controls NA Affymetrix, Illumina [510395] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081108 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01.00: Unspecified blepharitis (Gene-based burden) 1,280 European ancestry cases, 382,049 European ancestry controls NA Illumina [185271] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90083851 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E21: Hyperparathyroidism and other disorders of parathyroid gland 1,168 European ancestry cases, 386,457 European ancestry controls 2,417 European ancestry cases, 112,967 European ancestry controls Affymetrix, Illumina [510394] 0 hyperparathyroidism http://www.ebi.ac.uk/efo/EFO_0008506 GCST90079753 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01.009.: Unspecified blepharitis unspecified eye, unspecified eyelid (Gene-based burden) 1,280 European ancestry cases, 382,049 European ancestry controls NA Illumina [185271] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90083850 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G81: Hemiplegia and hemiparesis 2,070 European ancestry cases, 385,551 European ancestry controls NA Affymetrix, Illumina [510392] 0 hemiplegia, Hemiparesis http://www.ebi.ac.uk/efo/EFO_0009453, http://purl.obolibrary.org/obo/HP_0001269 GCST90079854 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02: Other disorders of eyelid (Gene-based burden) 7,325 European ancestry cases, 377,441 European ancestry controls NA Illumina [185300] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90083860 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04.2: Epiphora 1,139 European ancestry cases, 386,435 European ancestry controls NA Affymetrix, Illumina [510391] 0 Epiphora http://purl.obolibrary.org/obo/HP_0009926 GCST90079876 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.0: Entropion and trichiasis of eyelid (Gene-based burden) 838 European ancestry cases, 387,070 European ancestry controls NA Illumina [185344] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90083854 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E88: Other and unspecified metabolic disorders 580 European ancestry cases, 387,006 European ancestry controls NA Affymetrix, Illumina [510390] 0 metabolic disease http://www.ebi.ac.uk/efo/EFO_0000589 GCST90079780 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.1: Ectropion of eyelid (Gene-based burden) 581 European ancestry cases, 387,349 European ancestry controls NA Illumina [185344] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90083855 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40.5: Arthropathic psoriasis 1,104 European ancestry cases, 386,481 European ancestry controls NA Affymetrix, Illumina [510390] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90080347 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.3: Blepharochalasis (Gene-based burden) 883 European ancestry cases, 387,020 European ancestry controls NA Illumina [185344] 0 Ascher syndrome http://purl.obolibrary.org/obo/MONDO_0007198 GCST90083856 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E11.4: Type 2 diabetes mellitus with neurological complications 751 European ancestry cases, 386,815 European ancestry controls NA Affymetrix, Illumina [510389] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90079740 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.4: Ptosis of eyelid (Gene-based burden) 1,655 European ancestry cases, 386,181 European ancestry controls NA Illumina [185342] 0 ptosis http://purl.obolibrary.org/obo/MONDO_0000728 GCST90083857 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50: Crohn's disease [regional enteritis] 2,106 European ancestry cases, 385,486 European ancestry controls NA Affymetrix, Illumina [510389] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90080232 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.8: Other specified disorders of eyelid (Gene-based burden) 2,358 European ancestry cases, 385,294 European ancestry controls NA Illumina [185342] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90083858 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R47.8: Other speech disturbances 999 European ancestry cases, 386,616 European ancestry controls NA Affymetrix, Illumina [510387] 0 specific language disorder http://purl.obolibrary.org/obo/MONDO_0016226 GCST90080863 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.9: Unspecified disorder of eyelid (Gene-based burden) 856 European ancestry cases, 386,977 European ancestry controls NA Illumina [185334] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90083859 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I89.0: Lymphedema, not elsewhere classified 766 European ancestry cases, 386,832 European ancestry controls NA Affymetrix, Illumina [510386] 0 primary lymphedema http://purl.obolibrary.org/obo/MONDO_0019175 GCST90080079 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04: Disorders of lacrimal system (Gene-based burden) 5,367 European ancestry cases, 373,770 European ancestry controls NA Illumina [185172] 0 lacrimal apparatus disease http://www.ebi.ac.uk/efo/EFO_0009455 GCST90083864 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D69.6: Thrombocytopenia, unspecified 1,788 European ancestry cases, 385,791 European ancestry controls 3,725 European ancestry cases, 114,492 European ancestry controls Affymetrix, Illumina [510382] 0 Thrombocytopenia http://purl.obolibrary.org/obo/HP_0001873 GCST90079714 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04.1: Other disorders of lacrimal gland (Gene-based burden) 520 European ancestry cases, 387,404 European ancestry controls NA Illumina [185344] 0 disorder of lacrimal gland http://purl.obolibrary.org/obo/MONDO_0024625 GCST90083861 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W10.9: Fall on/from unspecified stairs and steps 1,246 European ancestry cases, 386,345 European ancestry controls NA Affymetrix, Illumina [510381] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081107 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04.2: Epiphora (Gene-based burden) 1,139 European ancestry cases, 386,435 European ancestry controls NA Illumina [185340] 0 Epiphora http://purl.obolibrary.org/obo/HP_0009926 GCST90083862 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.4: Fracture of malar, maxillary and zygoma bones 619 European ancestry cases, 386,946 European ancestry controls NA Affymetrix, Illumina [510379] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080948 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04.5: Stenosis and insufficiency of lacrimal passages (Gene-based burden) 1,351 European ancestry cases, 386,444 European ancestry controls NA Illumina [185344] 0 lacrimal apparatus disease http://www.ebi.ac.uk/efo/EFO_0009455 GCST90083863 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N36: Other disorders of urethra 964 European ancestry cases, 386,607 European ancestry controls NA Affymetrix, Illumina [510377] 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90080610 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H10: Conjunctivitis (Gene-based burden) 6,700 European ancestry cases, 362,087 European ancestry controls NA Illumina [184995] 0 conjunctivitis http://www.ebi.ac.uk/efo/EFO_0009450 GCST90083866 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R17: Unspecified jaundice 1,179 European ancestry cases, 386,397 European ancestry controls NA Affymetrix, Illumina [510377] 0 Jaundice http://purl.obolibrary.org/obo/HP_0000952 GCST90080806 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H10.9: Unspecified conjunctivitis (Gene-based burden) 1,400 European ancestry cases, 380,794 European ancestry controls NA Illumina [185245] 0 conjunctivitis http://www.ebi.ac.uk/efo/EFO_0009450 GCST90083865 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.20: Unspecified fracture of upper end of humerus 1,247 European ancestry cases, 386,325 European ancestry controls NA Affymetrix, Illumina [510377] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080976 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H11: Other disorders of conjunctiva (Gene-based burden) 1,714 European ancestry cases, 380,389 European ancestry controls NA Illumina [185253] 0 Conjunctival Disorder http://www.ebi.ac.uk/efo/EFO_1000203 GCST90083867 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D86: Sarcoidosis 782 European ancestry cases, 386,780 European ancestry controls NA Affymetrix, Illumina [510372] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90079720 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H16: Keratitis (Gene-based burden) 704 European ancestry cases, 385,576 European ancestry controls NA Illumina [185321] 0 keratitis http://www.ebi.ac.uk/efo/EFO_0009449 GCST90083868 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28.9: Disorder of kidney and ureter, unspecified 742 European ancestry cases, 386,838 European ancestry controls NA Affymetrix, Illumina [510365] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90080594 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H18: Other disorders of cornea (Gene-based burden) 1,087 European ancestry cases, 385,500 European ancestry controls NA Illumina [185327] 0 corneal disease http://www.ebi.ac.uk/efo/EFO_0009464 GCST90083869 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D07: Carcinoma in situ of other and unspecified genital organs 669 European ancestry cases, 386,937 European ancestry controls NA Affymetrix, Illumina [510364] 0 urogenital neoplasm http://www.ebi.ac.uk/efo/EFO_0003863 GCST90079651 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H20: Iridocyclitis (Gene-based burden) 1,094 European ancestry cases, 385,475 European ancestry controls NA Illumina [185329] 0 Iridocyclitis http://purl.obolibrary.org/obo/HP_0001094 GCST90083870 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I71: Aortic aneurysm and dissection 2,104 European ancestry cases, 385,413 European ancestry controls 4,254 European ancestry cases, 107,013 European ancestry controls Affymetrix, Illumina [510361] 0 aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0001666 GCST90080048 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25: Age-related cataract (Gene-based burden) 12,614 European ancestry cases, 375,168 European ancestry controls NA Illumina [185342] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90083875 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.0: Fracture of lumbar vertebra 745 European ancestry cases, 386,833 European ancestry controls NA Affymetrix, Illumina [510360] 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90080967 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.0: Age-related incipient cataract (Gene-based burden) 2,535 European ancestry cases, 385,395 European ancestry controls NA Illumina [185344] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90083871 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Rarely (UKB data field 20539) (Gene-based burden) 5,015 European ancestry cases, 38,023 European ancestry controls NA Illumina [137820] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082614 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08.3: Combined rheumatic disorders of mitral, aortic and tricuspid valves 608 European ancestry cases, 387,322 European ancestry controls NA Affymetrix, Illumina [510687] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90079960 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Sometimes (UKB data field 20539) (Gene-based burden) 19,262 European ancestry cases, 23,776 European ancestry controls NA Illumina [137820] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082615 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I27.2: Other secondary pulmonary hypertension 649 European ancestry cases, 387,279 European ancestry controls NA Affymetrix, Illumina [510687] 0 secondary hypertension http://www.ebi.ac.uk/efo/EFO_1002034 GCST90079986 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 500 Never (UKB data field 21034) (Gene-based burden) 56,841 European ancestry cases, 98,245 European ancestry controls NA Illumina [174051] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082713 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I67.9: Cerebrovascular disease, unspecified 1,469 European ancestry cases, 386,459 European ancestry controls NA Affymetrix, Illumina [510687] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90080040 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 501 Sometimes (UKB data field 21034) (Gene-based burden) 72,063 European ancestry cases, 83,023 European ancestry controls NA Illumina [174051] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082714 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I71.4: Abdominal aortic aneurysm, without rupture 1,184 European ancestry cases, 386,746 European ancestry controls NA Affymetrix, Illumina [510687] 0 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST90080047 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of loose mushy watery stools in the last three months - 502 Often (UKB data field 21034) (Gene-based burden) 18,197 European ancestry cases, 136,889 European ancestry controls NA Illumina [174051] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082715 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J38.7: Other diseases of larynx 594 European ancestry cases, 387,336 European ancestry controls NA Affymetrix, Illumina [510687] 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90080121 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73.9: Peripheral vascular disease, unspecified 3,601 European ancestry cases, 383,913 European ancestry controls NA Affymetrix, Illumina [510332] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90080050 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26.9: Unspecified cataract (Gene-based burden) 17,761 European ancestry cases, 369,666 European ancestry controls NA Illumina [185330] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083878 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M62.8: Other specified disorders of muscle 783 European ancestry cases, 386,702 European ancestry controls NA Affymetrix, Illumina [510329] 0 muscular disease http://www.ebi.ac.uk/efo/EFO_0002970 GCST90080514 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33: Retinal detachments and breaks (Gene-based burden) 4,015 European ancestry cases, 382,918 European ancestry controls NA Illumina [185337] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90083883 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A41.9: Sepsis, unspecified organism 4,673 European ancestry cases, 382,844 European ancestry controls 5,196 European ancestry cases, 114,497 European ancestry controls Affymetrix, Illumina [510328] 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90079545 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33.0: Retinal detachment with retinal break (Gene-based burden) 1,738 European ancestry cases, 386,192 European ancestry controls NA Illumina [185344] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90083880 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35.3: Polymyalgia rheumatica 2,040 European ancestry cases, 385,420 European ancestry controls NA Affymetrix, Illumina [510324] 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90080469 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33.2: Serous retinal detachment (Gene-based burden) 1,160 European ancestry cases, 386,573 European ancestry controls NA Illumina [185342] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90083881 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I63.9: Cerebral infarction, unspecified 3,386 European ancestry cases, 384,117 European ancestry controls NA Affymetrix, Illumina [510322] 0 cerebral infarction http://purl.obolibrary.org/obo/MONDO_0002679 GCST90080034 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33.3: Retinal breaks without detachment (Gene-based burden) 1,191 European ancestry cases, 386,593 European ancestry controls NA Illumina [185342] 0 retinal break http://www.ebi.ac.uk/efo/EFO_0010698 GCST90083882 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97.4: Presence of external hearing-aid 533 European ancestry cases, 386,972 European ancestry controls NA Affymetrix, Illumina [510317] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081431 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H34: Retinal vascular occlusions (Gene-based burden) 972 European ancestry cases, 386,217 European ancestry controls NA Illumina [185332] 0 retinal vein occlusion http://www.ebi.ac.uk/efo/EFO_1001157 GCST90083885 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.0: Bladder-neck obstruction 2,303 European ancestry cases, 385,191 European ancestry controls NA Affymetrix, Illumina [510315] 0 bladder neck obstruction http://www.ebi.ac.uk/efo/EFO_1000840 GCST90080603 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H34.8: Other retinal vascular occlusions (Gene-based burden) 539 European ancestry cases, 387,344 European ancestry controls NA Illumina [185344] 0 retinal vein occlusion http://www.ebi.ac.uk/efo/EFO_1001157 GCST90083884 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G83: Other paralytic syndromes 539 European ancestry cases, 386,953 European ancestry controls NA Affymetrix, Illumina [510313] 0 paralytic strabismus http://www.ebi.ac.uk/efo/EFO_0009678 GCST90079855 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L97: Non-pressure chronic ulcer of lower limb, not elsewhere classified 1,708 European ancestry cases, 385,756 European ancestry controls NA Affymetrix, Illumina [510281] 0 ulcer of lower limb http://www.ebi.ac.uk/efo/EFO_0007068 GCST90080381 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H44: Disorders of globe (Gene-based burden) 646 European ancestry cases, 386,049 European ancestry controls NA Illumina [185328] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083899 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A41: Other sepsis 5,918 European ancestry cases, 381,545 European ancestry controls 5,534 European ancestry cases, 114,497 European ancestry controls Affymetrix, Illumina [510280] 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90079546 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H47: Other disorders of optic [2nd] nerve and visual pathways (Gene-based burden) 511 European ancestry cases, 386,640 European ancestry controls NA Illumina [185333] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083900 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G93.3: Postviral fatigue syndrome 817 European ancestry cases, 386,637 European ancestry controls NA Affymetrix, Illumina [510280] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90079857 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H50: Other strabismus (Gene-based burden) 1,194 European ancestry cases, 385,387 European ancestry controls NA Illumina [185325] 0 Strabismus http://purl.obolibrary.org/obo/HP_0000486 GCST90083901 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.4: Other specified urinary incontinence 2,037 European ancestry cases, 385,439 European ancestry controls NA Affymetrix, Illumina [510280] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90080613 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H52: Disorders of refraction and accommodation (Gene-based burden) 2,691 European ancestry cases, 383,414 European ancestry controls NA Illumina [185308] 0 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST90083903 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G62.9: Polyneuropathy, unspecified 1,543 European ancestry cases, 385,937 European ancestry controls NA Affymetrix, Illumina [510279] 0 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90079849 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H52.1: Myopia (Gene-based burden) 1,781 European ancestry cases, 386,149 European ancestry controls NA Illumina [185344] 0 Myopia http://purl.obolibrary.org/obo/HP_0000545 GCST90083902 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D47: Other neoplasms of uncertain behavior of lymphoid, hematopoietic and related tissue 987 European ancestry cases, 386,440 European ancestry controls 1,752 European ancestry cases, 114,182 European ancestry controls Affymetrix, Illumina [510272] 2 GCST90079699 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53: Visual disturbances (Gene-based burden) 5,174 European ancestry cases, 375,749 European ancestry controls NA Illumina [185244] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90083909 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z41: Encounter for procedures for purposes other than remedying health state 914 European ancestry cases, 386,561 European ancestry controls NA Affymetrix, Illumina [510270] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081256 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.0: Amblyopia ex anopsia (Gene-based burden) 794 European ancestry cases, 386,946 European ancestry controls NA Illumina [185343] 0 amblyopia http://purl.obolibrary.org/obo/MONDO_0001020 GCST90083904 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.8: Allergy status to other drugs, medicaments and biological substances status 7,086 European ancestry cases, 380,334 European ancestry controls NA Affymetrix, Illumina [510266] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081386 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.1: Subjective visual disturbances (Gene-based burden) 609 European ancestry cases, 386,755 European ancestry controls NA Illumina [185340] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90083905 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83.7: Family history of diseases of the digestive system 947 European ancestry cases, 386,486 European ancestry controls 464 European ancestry cases, 33,304 European ancestry controls Affymetrix, Illumina [510265] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081342 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.2: Diplopia (Gene-based burden) 923 European ancestry cases, 387,007 European ancestry controls NA Illumina [185344] 0 Diplopia http://purl.obolibrary.org/obo/HP_0000651 GCST90083906 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26.9: Unspecified cataract 17,761 European ancestry cases, 369,666 European ancestry controls 7,390 European ancestry cases, 103,681 European ancestry controls Affymetrix, Illumina [510261] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90079892 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.8: Other visual disturbances (Gene-based burden) 934 European ancestry cases, 386,978 European ancestry controls NA Illumina [185344] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90083907 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J15: Bacterial pneumonia, not elsewhere classified 715 European ancestry cases, 386,722 European ancestry controls NA Affymetrix, Illumina [510261] 0 bacterial pneumonia http://www.ebi.ac.uk/efo/EFO_1001272 GCST90080094 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.9: Unspecified visual disturbance (Gene-based burden) 667 European ancestry cases, 385,885 European ancestry controls NA Illumina [185311] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90083908 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K27: Peptic ulcer, site unspecified 583 European ancestry cases, 386,834 European ancestry controls NA Affymetrix, Illumina [510261] 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90080200 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H54: Blindness and low vision (Gene-based burden) 1,725 European ancestry cases, 384,291 European ancestry controls NA Illumina [185313] 0 Visual impairment http://purl.obolibrary.org/obo/HP_0000505 GCST90083910 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R04.2: Hemoptysis 2,545 European ancestry cases, 384,924 European ancestry controls NA Affymetrix, Illumina [510255] 0 Hemoptysis http://purl.obolibrary.org/obo/HP_0002105 GCST90080762 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.2: Neuralgia and neuritis, unspecified 585 European ancestry cases, 386,972 European ancestry controls NA Affymetrix, Illumina [510358] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90080545 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.1: Age-related nuclear cataract (Gene-based burden) 7,306 European ancestry cases, 380,624 European ancestry controls NA Illumina [185344] 0 Age-related nuclear cataract http://purl.obolibrary.org/obo/HP_0011142 GCST90083872 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T40: Poisoning by, adverse effect of and underdosing of narcotics and psychodysleptics [hallucinogens] 860 European ancestry cases, 386,651 European ancestry controls NA Affymetrix, Illumina [510356] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081052 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.8: Other age-related cataract (Gene-based burden) 2,425 European ancestry cases, 385,472 European ancestry controls NA Illumina [185343] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90083873 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I20.0: Unstable angina 6,110 European ancestry cases, 381,435 European ancestry controls NA Affymetrix, Illumina [510353] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90079965 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H25.9: Unspecified age-related cataract (Gene-based burden) 1,887 European ancestry cases, 386,041 European ancestry controls NA Illumina [185344] 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90083874 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S32.00: Fracture of unspecified lumbar vertebra 643 European ancestry cases, 386,917 European ancestry controls NA Affymetrix, Illumina [510348] 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90080966 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26: Other cataract (Gene-based burden) 20,291 European ancestry cases, 364,151 European ancestry controls NA Illumina [185284] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083879 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K85: Acute pancreatitis 2,460 European ancestry cases, 385,091 European ancestry controls NA Affymetrix, Illumina [510338] 0 acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1000652 GCST90080310 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26.4: Secondary cataract (Gene-based burden) 1,813 European ancestry cases, 386,117 European ancestry controls NA Illumina [185344] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083876 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.3: Sleep apnea 5,862 European ancestry cases, 381,677 European ancestry controls NA Affymetrix, Illumina [510336] 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90079833 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H26.8: Other specified cataract (Gene-based burden) 787 European ancestry cases, 387,143 European ancestry controls NA Illumina [185344] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083877 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 92 (UKB data field 5699) (Gene-based burden) 1,112 European ancestry cases, 32,967 European ancestry controls NA Illumina [127586] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083358 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.94: Osteoarthritis, unspecified site 1,597 European ancestry cases, 386,333 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080423 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 93 (UKB data field 5699) (Gene-based burden) 2,325 European ancestry cases, 31,754 European ancestry controls NA Illumina [127586] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083359 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.97: Osteoarthritis, unspecified site 3,143 European ancestry cases, 384,787 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080424 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 94 (UKB data field 5699) (Gene-based burden) 1,838 European ancestry cases, 32,241 European ancestry controls NA Illumina [127586] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083360 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.99: Osteoarthritis, unspecified site 5,421 European ancestry cases, 382,509 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080425 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 95 (UKB data field 5699) (Gene-based burden) 27,553 European ancestry cases, 6,526 European ancestry controls NA Illumina [127586] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083361 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.2: Hallux rigidus 1,822 European ancestry cases, 386,108 European ancestry controls NA Affymetrix, Illumina [510688] 0 Hallux rigidus http://purl.obolibrary.org/obo/HP_0025004 GCST90080429 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 96 (UKB data field 5699) (Gene-based burden) 1,723 European ancestry cases, 32,356 European ancestry controls NA Illumina [127586] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083362 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.22: Derangement of posterior horn of medial meniscus due to old tear or injury 3,389 European ancestry cases, 384,541 European ancestry controls NA Affymetrix, Illumina [510688] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080435 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - anxious (UKB data field 20185) (Gene-based burden) 1,927 European ancestry cases, 7,137 European ancestry controls NA Illumina [72407] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082352 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.23: Derangement of other medial meniscus due to old tear or injury 4,501 European ancestry cases, 383,429 European ancestry controls NA Affymetrix, Illumina [510688] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080436 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - anxious (UKB data field 5779) (Gene-based burden) 4,436 European ancestry cases, 15,928 European ancestry controls NA Illumina [106737] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083364 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.57: Low back pain 1,038 European ancestry cases, 386,892 European ancestry controls NA Affymetrix, Illumina [510688] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90080508 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 5 (UKB data field 20171) (Gene-based burden) 5,923 European ancestry cases, 103,014 European ancestry controls NA Illumina [166662] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082321 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.59: Low back pain 2,457 European ancestry cases, 385,473 European ancestry controls NA Affymetrix, Illumina [510688] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90080509 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 5 (UKB data field 4968) (Gene-based burden) 8,230 European ancestry cases, 148,723 European ancestry controls NA Illumina [174673] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083225 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.99: Dorsalgia, unspecified 2,029 European ancestry cases, 385,901 European ancestry controls NA Affymetrix, Illumina [510688] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90080511 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI4 positional arithmetic - 6 (UKB data field 20171) (Gene-based burden) 96,930 European ancestry cases, 12,007 European ancestry controls NA Illumina [166662] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082322 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.4: Personal history of major surgery, not elsewhere classified 1,702 European ancestry cases, 386,228 European ancestry controls NA Affymetrix, Illumina [510688] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081408 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 503 Most of the time (UKB data field 21032) (Gene-based burden) 4,007 European ancestry cases, 79,139 European ancestry controls NA Illumina [159641] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082706 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.6: Personal history of chemotherapy for neoplastic disease 4,641 European ancestry cases, 383,289 European ancestry controls NA Affymetrix, Illumina [510688] 0 neoplastic disease or syndrome http://purl.obolibrary.org/obo/MONDO_0023370 GCST90081409 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 504 Always (UKB data field 21032) (Gene-based burden) 1,280 European ancestry cases, 81,866 European ancestry controls NA Illumina [159641] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082707 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.8: Presence of other specified functional implants 1,112 European ancestry cases, 386,818 European ancestry controls NA Affymetrix, Illumina [510688] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081429 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Daily or almost daily (UKB data field 20413) (Gene-based burden) 653 European ancestry cases, 75,890 European ancestry controls NA Illumina [156061] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082411 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B96.1: Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified elsewhere 525 European ancestry cases, 387,405 European ancestry controls NA Affymetrix, Illumina [510687] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079565 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Less than monthly (UKB data field 20413) (Gene-based burden) 5,368 European ancestry cases, 71,175 European ancestry controls NA Illumina [156085] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082408 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.7: Other and unspecified malignant neoplasm of skin of lower limb, including hip 1,262 European ancestry cases, 386,666 European ancestry controls NA Affymetrix, Illumina [510687] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079600 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Monthly (UKB data field 20413) (Gene-based burden) 1,374 European ancestry cases, 75,169 European ancestry controls NA Illumina [156085] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082409 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.9: Secondary and unspecified malignant neoplasm of lymph node, unspecified 650 European ancestry cases, 387,279 European ancestry controls NA Affymetrix, Illumina [510687] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079619 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Never (UKB data field 20413) (Gene-based burden) 67,661 European ancestry cases, 8,882 European ancestry controls NA Illumina [156085] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082407 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C80.9: Malignant neoplasm, unspecified 572 European ancestry cases, 387,358 European ancestry controls NA Affymetrix, Illumina [510687] 0 GCST90079631 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Weekly (UKB data field 20413) (Gene-based burden) 1,487 European ancestry cases, 75,056 European ancestry controls NA Illumina [156085] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082410 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C85.1: Unspecified B-cell lymphoma 521 European ancestry cases, 387,409 European ancestry controls NA Affymetrix, Illumina [510687] 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90079636 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Never (UKB data field 20539) (Gene-based burden) 665 European ancestry cases, 42,373 European ancestry controls NA Illumina [137820] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082613 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F05.9: Delirium, unspecified 1,083 European ancestry cases, 386,847 European ancestry controls NA Affymetrix, Illumina [510687] 0 delirium http://www.ebi.ac.uk/efo/EFO_0009267 GCST90079785 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to stop worrying during worst period of anxiety - Often (UKB data field 20539) (Gene-based burden) 18,096 European ancestry cases, 24,942 European ancestry controls NA Illumina [137820] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082616 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G51.0: Bell's palsy 878 European ancestry cases, 387,048 European ancestry controls NA Affymetrix, Illumina [510687] 0 Bell's palsy http://www.ebi.ac.uk/efo/EFO_0007167 GCST90079838 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI13 subset inclusion logic - False (UKB data field 5866) (Gene-based burden) 1,119 European ancestry cases, 2,084 European ancestry controls NA Illumina [36508] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083380 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.82: Other spondylosis 2,593 European ancestry cases, 385,337 European ancestry controls NA Affymetrix, Illumina [510688] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080480 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI13 subset inclusion logic - Neither true nor false (UKB data field 5866) (Gene-based burden) 868 European ancestry cases, 2,335 European ancestry controls NA Illumina [36508] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083382 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.86: Other spondylosis 1,930 European ancestry cases, 386,000 European ancestry controls NA Affymetrix, Illumina [510688] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080481 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI13 subset inclusion logic (UKB data field 5866) (Gene-based burden) 1,283 European ancestry cases, 1,920 European ancestry controls NA Illumina [36508] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083381 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.92: Spondylosis, unspecified 893 European ancestry cases, 387,037 European ancestry controls NA Affymetrix, Illumina [510688] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080483 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 714 (UKB data field 20167) (Gene-based burden) 828 European ancestry cases, 108,657 European ancestry controls NA Illumina [166796] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082317 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.96: Spondylosis, unspecified 955 European ancestry cases, 386,975 European ancestry controls NA Affymetrix, Illumina [510688] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080484 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 987 (UKB data field 20167) (Gene-based burden) 108,555 European ancestry cases, 930 European ancestry controls NA Illumina [166796] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082316 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48.02: Spinal stenosis, cervical region 607 European ancestry cases, 387,323 European ancestry controls NA Affymetrix, Illumina [510688] 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90080487 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 714 (UKB data field 4946) (Gene-based burden) 1,083 European ancestry cases, 170,999 European ancestry controls NA Illumina [176541] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083220 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48.06: Spinal stenosis, lumbar region 3,396 European ancestry cases, 384,534 European ancestry controls NA Affymetrix, Illumina [510688] 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90080488 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI2 identify largest number - 987 (UKB data field 4946) (Gene-based burden) 170,897 European ancestry cases, 1,185 European ancestry controls NA Illumina [176541] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083221 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50.3: Other cervical disc degeneration 516 European ancestry cases, 387,414 European ancestry controls NA Affymetrix, Illumina [510688] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90080493 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - adult (UKB data field 20169) (Gene-based burden) 91,437 European ancestry cases, 18,036 European ancestry controls NA Illumina [166794] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082320 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51.2: Other thoracic, thoracolumbar and lumbosacral intervertebral disc displacement 3,205 European ancestry cases, 384,725 European ancestry controls NA Affymetrix, Illumina [510688] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90080496 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - adult (UKB data field 4957) (Gene-based burden) 147,135 European ancestry cases, 24,190 European ancestry controls NA Illumina [176437] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083224 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.1: Radiculopathy 1,154 European ancestry cases, 386,776 European ancestry controls NA Affymetrix, Illumina [510688] 0 radiculopathy http://purl.obolibrary.org/obo/MONDO_0002959 GCST90080500 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - develop (UKB data field 20169) (Gene-based burden) 7,762 European ancestry cases, 101,711 European ancestry controls NA Illumina [166794] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082319 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.22: Cervicalgia 1,083 European ancestry cases, 386,847 European ancestry controls NA Affymetrix, Illumina [510688] 0 Neck pain http://purl.obolibrary.org/obo/HP_0030833 GCST90080501 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - develop (UKB data field 4957) (Gene-based burden) 7,895 European ancestry cases, 163,430 European ancestry controls NA Illumina [176437] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083223 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.39: Sciatica 681 European ancestry cases, 387,249 European ancestry controls NA Affymetrix, Illumina [510688] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90080504 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - grow (UKB data field 20169) (Gene-based burden) 10,072 European ancestry cases, 99,401 European ancestry controls NA Illumina [166794] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082318 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.56: Low back pain 2,859 European ancestry cases, 385,071 European ancestry controls NA Affymetrix, Illumina [510688] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90080507 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI3 word interpolation - grow (UKB data field 4957) (Gene-based burden) 18,400 European ancestry cases, 152,925 European ancestry controls NA Illumina [176437] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083222 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.26: Derangement of other lateral meniscus due to old tear or injury 1,311 European ancestry cases, 386,619 European ancestry controls NA Affymetrix, Illumina [510688] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080437 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - calm (UKB data field 5779) (Gene-based burden) 717 European ancestry cases, 19,647 European ancestry controls NA Illumina [106737] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083363 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.33: Other meniscus derangements, other medial meniscus 1,491 European ancestry cases, 386,439 European ancestry controls NA Affymetrix, Illumina [510688] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080441 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - tense (UKB data field 20185) (Gene-based burden) 6,747 European ancestry cases, 2,317 European ancestry controls NA Illumina [72407] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082353 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.36: Other meniscus derangements, other lateral meniscus 671 European ancestry cases, 387,259 European ancestry controls NA Affymetrix, Illumina [510688] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080442 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - tense (UKB data field 5779) (Gene-based burden) 14,752 European ancestry cases, 5,612 European ancestry controls NA Illumina [106737] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083366 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.4: Loose body in knee 1,046 European ancestry cases, 386,884 European ancestry controls NA Affymetrix, Illumina [510688] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080444 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI11 antonym - worried (UKB data field 5779) (Gene-based burden) 869 European ancestry cases, 19,495 European ancestry controls NA Illumina [106737] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083365 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.46: Effusion, knee 969 European ancestry cases, 386,961 European ancestry controls NA Affymetrix, Illumina [510688] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080451 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 45 (UKB data field 20187) (Gene-based burden) 2,481 European ancestry cases, 3,347 European ancestry controls NA Illumina [55700] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082357 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.51: Pain in shoulder 1,380 European ancestry cases, 386,550 European ancestry controls NA Affymetrix, Illumina [510688] 0 Shoulder pain http://purl.obolibrary.org/obo/HP_0030834 GCST90080454 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 47 (UKB data field 20187) (Gene-based burden) 561 European ancestry cases, 5,267 European ancestry controls NA Illumina [55700] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082356 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.55: Pain in hip 2,188 European ancestry cases, 385,742 European ancestry controls NA Affymetrix, Illumina [510688] 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90080455 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 49 (UKB data field 20187) (Gene-based burden) 981 European ancestry cases, 4,847 European ancestry controls NA Illumina [55700] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082355 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.76: Osteophyte, knee 874 European ancestry cases, 387,056 European ancestry controls NA Affymetrix, Illumina [510688] 0 exostosis http://purl.obolibrary.org/obo/MONDO_0002181 GCST90080462 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 50 (UKB data field 20187) (Gene-based burden) 1,353 European ancestry cases, 4,475 European ancestry controls NA Illumina [55700] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082354 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.77: Osteophyte, ankle and foot 1,044 European ancestry cases, 386,886 European ancestry controls NA Affymetrix, Illumina [510688] 0 exostosis http://purl.obolibrary.org/obo/MONDO_0002181 GCST90080463 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 45 (UKB data field 5790) (Gene-based burden) 3,466 European ancestry cases, 4,946 European ancestry controls NA Illumina [69977] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083367 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M43.16: Spondylolisthesis, lumbar region 1,184 European ancestry cases, 386,746 European ancestry controls NA Affymetrix, Illumina [510688] 0 spondylolisthesis http://www.ebi.ac.uk/efo/EFO_0007493 GCST90080473 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 48 (UKB data field 5790) (Gene-based burden) 895 European ancestry cases, 7,517 European ancestry controls NA Illumina [69977] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083368 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M46.9: Unspecified inflammatory spondylopathy 1,437 European ancestry cases, 386,493 European ancestry controls NA Affymetrix, Illumina [510688] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90080476 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 49 (UKB data field 5790) (Gene-based burden) 1,344 European ancestry cases, 7,068 European ancestry controls NA Illumina [69977] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083369 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.2: Other spondylosis with radiculopathy 761 European ancestry cases, 387,169 European ancestry controls NA Affymetrix, Illumina [510688] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080478 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI12 square sequence recognition - 50 (UKB data field 5790) (Gene-based burden) 2,051 European ancestry cases, 6,361 European ancestry controls NA Illumina [69977] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083370 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.80: Other spondylosis 503 European ancestry cases, 387,427 European ancestry controls NA Affymetrix, Illumina [510688] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080479 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D75: Other and unspecified diseases of blood and blood-forming organs 993 European ancestry cases, 386,043 European ancestry controls 2,694 European ancestry cases, 113,782 European ancestry controls Affymetrix, Illumina [509884] 1 hematologic disease http://www.ebi.ac.uk/efo/EFO_0005803 GCST90079719 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I64: Stroke, not specified as haemorrhage or infarction (Gene-based burden) 1,987 European ancestry cases, 384,940 European ancestry controls NA Illumina [185321] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90084022 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28: Other disorders of kidney and ureter, not elsewhere classified 3,413 European ancestry cases, 383,589 European ancestry controls 7,614 European ancestry cases, 110,159 European ancestry controls Affymetrix, Illumina [509878] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90080595 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I65: Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction (Gene-based burden) 1,329 European ancestry cases, 386,456 European ancestry controls NA Illumina [185342] 0 occlusion precerebral artery http://www.ebi.ac.uk/efo/EFO_0009677 GCST90084024 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D21: Other benign neoplasms of connective and other soft tissue 729 European ancestry cases, 386,265 European ancestry controls NA Affymetrix, Illumina [509874] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079672 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I65.2: Occlusion and stenosis of carotid artery (Gene-based burden) 1,229 European ancestry cases, 386,700 European ancestry controls NA Illumina [185327] 0 carotid artery thrombosis http://www.ebi.ac.uk/efo/EFO_1000853 GCST90084023 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N13: Obstructive and reflux uropathy 3,650 European ancestry cases, 383,346 European ancestry controls NA Affymetrix, Illumina [509870] 0 urinary tract obstruction http://www.ebi.ac.uk/efo/EFO_0009571 GCST90080578 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.96: Arthritis, unspecified (Gene-based burden) 1,141 European ancestry cases, 386,789 European ancestry controls NA Illumina [185344] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90084387 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.7: Personal history of diseases of the circulatory system 22,886 European ancestry cases, 360,766 European ancestry controls NA Affymetrix, Illumina [507051] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90081364 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.97: Arthritis, unspecified (Gene-based burden) 774 European ancestry cases, 387,156 European ancestry controls NA Illumina [185344] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90084388 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R53.83: Other fatigue 938 European ancestry cases, 382,816 European ancestry controls NA Affymetrix, Illumina [507048] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90080876 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.99: Arthritis, unspecified (Gene-based burden) 4,690 European ancestry cases, 383,240 European ancestry controls NA Illumina [185344] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90084389 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R45.8: Other symptoms and signs involving emotional state 1,457 European ancestry cases, 382,413 European ancestry controls NA Affymetrix, Illumina [507028] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90080860 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M15: Polyosteoarthritis (Gene-based burden) 6,260 European ancestry cases, 378,716 European ancestry controls NA Illumina [185307] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084394 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R49: Voice and resonance disorders 2,270 European ancestry cases, 381,451 European ancestry controls NA Affymetrix, Illumina [506992] 0 voice disorders http://www.ebi.ac.uk/efo/EFO_0009692 GCST90080867 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M15.0: Primary generalized (osteo)arthritis (Gene-based burden) 550 European ancestry cases, 387,380 European ancestry controls NA Illumina [185344] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084392 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W64: Exposure to other animate mechanical forces 748 European ancestry cases, 382,877 European ancestry controls NA Affymetrix, Illumina [506982] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081133 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M15.9: Polyosteoarthritis, unspecified (Gene-based burden) 5,066 European ancestry cases, 382,725 European ancestry controls NA Illumina [185344] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084393 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29.8: Other symptoms and signs involving the nervous and musculoskeletal systems 2,856 European ancestry cases, 380,793 European ancestry controls NA Affymetrix, Illumina [506981] 0 Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000924 GCST90080835 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16: Osteoarthritis of hip (Gene-based burden) 15,772 European ancestry cases, 369,426 European ancestry controls NA Illumina [185286] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90084398 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.39: Encounter for other screening for malignant neoplasm of breast 1,943 European ancestry cases, 381,627 European ancestry controls NA Affymetrix, Illumina [506971] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081208 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16.0: Bilateral primary osteoarthritis of hip (Gene-based burden) 884 European ancestry cases, 387,046 European ancestry controls NA Illumina [185344] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90084395 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L70: Acne 1,390 European ancestry cases, 382,295 European ancestry controls NA Affymetrix, Illumina [506970] 0 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST90080359 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16.1: Unilateral primary osteoarthritis of hip (Gene-based burden) 3,961 European ancestry cases, 383,969 European ancestry controls NA Illumina [185344] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90084396 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52.9: Noninfective gastroenteritis and colitis, unspecified 17,883 European ancestry cases, 365,747 European ancestry controls NA Affymetrix, Illumina [506966] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90080236 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.22: Derangement of posterior horn of medial meniscus due to old tear or injury (Gene-based burden) 3,389 European ancestry cases, 384,541 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084421 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R55: Syncope and collapse 12,288 European ancestry cases, 370,934 European ancestry controls NA Affymetrix, Illumina [506522] 0 Syncope http://purl.obolibrary.org/obo/HP_0001279 GCST90080880 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.23: Derangement of other medial meniscus due to old tear or injury (Gene-based burden) 4,501 European ancestry cases, 383,429 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084422 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51: Thoracic, thoracolumbar, and lumbosacral intervertebral disc disorders 10,022 European ancestry cases, 373,202 European ancestry controls NA Affymetrix, Illumina [506521] 0 discitis http://www.ebi.ac.uk/efo/EFO_1000900 GCST90080498 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.26: Derangement of other lateral meniscus due to old tear or injury (Gene-based burden) 1,311 European ancestry cases, 386,619 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084423 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.3: Personal history of diseases of the musculoskeletal system and connective tissue 3,459 European ancestry cases, 379,603 European ancestry controls NA Affymetrix, Illumina [506474] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081371 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.3: Other meniscus derangements (Gene-based burden) 4,543 European ancestry cases, 383,357 European ancestry controls NA Illumina [185343] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084429 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R94.3: Abnormal results of cardiovascular function studies 1,315 European ancestry cases, 381,670 European ancestry controls NA Affymetrix, Illumina [506463] 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90080935 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.30: Other meniscus derangements, unspecified meniscus (Gene-based burden) 591 European ancestry cases, 387,307 European ancestry controls NA Illumina [185340] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084425 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I67: Other cerebrovascular diseases (Gene-based burden) 3,818 European ancestry cases, 383,266 European ancestry controls NA Illumina [185316] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90084027 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D69: Purpura and other hemorrhagic conditions 2,456 European ancestry cases, 384,489 European ancestry controls 4,743 European ancestry cases, 114,492 European ancestry controls Affymetrix, Illumina [509861] 1 hemorrhagic disease http://purl.obolibrary.org/obo/MONDO_0002243 GCST90079715 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I67.8: Other specified cerebrovascular diseases (Gene-based burden) 1,481 European ancestry cases, 386,449 European ancestry controls NA Illumina [185344] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90084025 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.8: Other specified symptoms and signs involving the digestive system and abdomen 2,178 European ancestry cases, 384,747 European ancestry controls NA Affymetrix, Illumina [509858] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90080812 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I67.9: Cerebrovascular disease, unspecified (Gene-based burden) 1,469 European ancestry cases, 386,459 European ancestry controls NA Illumina [185344] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90084026 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R56: Convulsions, not elsewhere classified 2,932 European ancestry cases, 384,060 European ancestry controls NA Affymetrix, Illumina [509857] 0 Seizure http://purl.obolibrary.org/obo/HP_0001250 GCST90080883 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I69: Sequelae of cerebrovascular disease (Gene-based burden) 1,714 European ancestry cases, 386,210 European ancestry controls NA Illumina [185344] 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90084029 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A49: Bacterial infection of unspecified site 1,117 European ancestry cases, 385,841 European ancestry controls NA Affymetrix, Illumina [509849] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079547 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I69.4: Sequelae of stroke, not specified as haemorrhage or infarction (Gene-based burden) 1,221 European ancestry cases, 386,709 European ancestry controls NA Illumina [185344] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90084028 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I86: Varicose veins of other sites 766 European ancestry cases, 386,186 European ancestry controls NA Affymetrix, Illumina [509847] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90080077 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I70: Atherosclerosis (Gene-based burden) 1,790 European ancestry cases, 385,917 European ancestry controls NA Illumina [185340] 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90084032 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J18.9: Pneumonia, unspecified organism 6,141 European ancestry cases, 380,836 European ancestry controls NA Affymetrix, Illumina [509846] 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90080097 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I70.2: Atherosclerosis of native arteries of the extremities (Gene-based burden) 1,065 European ancestry cases, 386,835 European ancestry controls NA Illumina [185342] 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90084031 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48: Other spondylopathies 5,848 European ancestry cases, 381,138 European ancestry controls NA Affymetrix, Illumina [509845] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90080490 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I70.20: Unspecified atherosclerosis of native arteries of extremities (Gene-based burden) 509 European ancestry cases, 387,414 European ancestry controls NA Illumina [185342] 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90084030 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I64: Stroke, not specified as haemorrhage or infarction 1,987 European ancestry cases, 384,940 European ancestry controls NA Affymetrix, Illumina [509844] 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90080036 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S89.90: Unspecified injury of unspecified lower leg 915 European ancestry cases, 381,599 European ancestry controls NA Affymetrix, Illumina [506088] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081034 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.6: Stiffness of joint, not elsewhere classified (Gene-based burden) 803 European ancestry cases, 386,439 European ancestry controls NA Illumina [185312] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90084447 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29: Gastritis and duodenitis 37,321 European ancestry cases, 345,285 European ancestry controls NA Affymetrix, Illumina [506086] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90080208 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.7: Osteophyte (Gene-based burden) 3,804 European ancestry cases, 384,122 European ancestry controls NA Illumina [185344] 0 exostosis http://purl.obolibrary.org/obo/MONDO_0002181 GCST90084450 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R25: Abnormal involuntary movements 2,585 European ancestry cases, 379,959 European ancestry controls NA Affymetrix, Illumina [506081] 0 Abnormality of movement http://purl.obolibrary.org/obo/HP_0100022 GCST90080828 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.76: Osteophyte, knee (Gene-based burden) 874 European ancestry cases, 387,056 European ancestry controls NA Illumina [185344] 0 exostosis http://purl.obolibrary.org/obo/MONDO_0002181 GCST90084448 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.8: Other long term (current) drug therapy 5,294 European ancestry cases, 377,396 European ancestry controls NA Affymetrix, Illumina [506076] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081327 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.77: Osteophyte, ankle and foot (Gene-based burden) 1,044 European ancestry cases, 386,886 European ancestry controls NA Illumina [185344] 0 exostosis http://purl.obolibrary.org/obo/MONDO_0002181 GCST90084449 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72.0: Epidermal cyst 4,196 European ancestry cases, 378,535 European ancestry controls NA Affymetrix, Illumina [506065] 0 Epidermal Inclusion Cyst http://www.ebi.ac.uk/efo/EFO_1000243 GCST90080361 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.8: Other specified joint disorders (Gene-based burden) 1,019 European ancestry cases, 385,981 European ancestry controls NA Illumina [185309] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90084451 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S69.9: Unspecified injury of wrist, hand and finger(s) 1,134 European ancestry cases, 381,363 European ancestry controls NA Affymetrix, Illumina [506013] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081008 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M31: Other necrotizing vasculopathies (Gene-based burden) 855 European ancestry cases, 386,913 European ancestry controls NA Illumina [185341] 0 vasculitis http://www.ebi.ac.uk/efo/EFO_0006803 GCST90084453 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S69.90: Unspecified injury of unspecified wrist, hand and finger(s) 937 European ancestry cases, 381,550 European ancestry controls NA Affymetrix, Illumina [506004] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081007 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35: Other systemic involvement of connective tissue (Gene-based burden) 3,379 European ancestry cases, 383,362 European ancestry controls NA Illumina [185312] 0 connective tissue disease http://www.ebi.ac.uk/efo/EFO_1001986 GCST90084456 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B34.9: Viral infection, unspecified 3,710 European ancestry cases, 378,790 European ancestry controls NA Affymetrix, Illumina [506002] 0 viral disease http://www.ebi.ac.uk/efo/EFO_0000763 GCST90079551 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35.0: Sicca syndrome (Gene-based burden) 711 European ancestry cases, 387,080 European ancestry controls NA Illumina [185333] 0 Sjogren syndrome http://www.ebi.ac.uk/efo/EFO_0000699 GCST90084454 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S89: Other and unspecified injuries of lower leg 1,229 European ancestry cases, 381,176 European ancestry controls NA Affymetrix, Illumina [505997] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081036 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35.3: Polymyalgia rheumatica (Gene-based burden) 2,040 European ancestry cases, 385,420 European ancestry controls NA Illumina [185333] 0 polymyalgia rheumatica http://www.ebi.ac.uk/efo/EFO_0008518 GCST90084455 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.9: Respiratory disorder, unspecified 14,771 European ancestry cases, 367,671 European ancestry controls NA Affymetrix, Illumina [505980] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080161 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M41: Scoliosis (Gene-based burden) 1,582 European ancestry cases, 385,435 European ancestry controls NA Illumina [185331] 0 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST90084458 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S69: Other and unspecified injuries of wrist, hand and finger(s) 1,200 European ancestry cases, 381,238 European ancestry controls NA Affymetrix, Illumina [505950] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081009 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M41.9: Scoliosis, unspecified (Gene-based burden) 1,360 European ancestry cases, 386,551 European ancestry controls NA Illumina [185344] 0 scoliosis http://www.ebi.ac.uk/efo/EFO_0004273 GCST90084457 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.4: Change in bowel habit 15,857 European ancestry cases, 366,696 European ancestry controls NA Affymetrix, Illumina [505940] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90080809 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M43: Other deforming dorsopathies (Gene-based burden) 2,743 European ancestry cases, 381,483 European ancestry controls NA Illumina [185272] 0 skeletal system disease http://www.ebi.ac.uk/efo/EFO_0002461 GCST90084461 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R79.8: Other specified abnormal findings of blood chemistry 11,085 European ancestry cases, 371,365 European ancestry controls NA Affymetrix, Illumina [505902] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080910 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I71: Aortic aneurysm and dissection (Gene-based burden) 2,104 European ancestry cases, 385,413 European ancestry controls NA Illumina [185340] 0 aortic aneurysm http://www.ebi.ac.uk/efo/EFO_0001666 GCST90084034 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.8: Other specified joint disorders 1,019 European ancestry cases, 385,981 European ancestry controls NA Affymetrix, Illumina [509834] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90080465 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I71.4: Abdominal aortic aneurysm, without rupture (Gene-based burden) 1,184 European ancestry cases, 386,746 European ancestry controls NA Illumina [185344] 0 Abdominal Aortic Aneurysm http://www.ebi.ac.uk/efo/EFO_0004214 GCST90084033 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G62: Other and unspecified polyneuropathies 1,972 European ancestry cases, 384,992 European ancestry controls NA Affymetrix, Illumina [509833] 0 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90079850 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73: Other peripheral vascular diseases (Gene-based burden) 5,786 European ancestry cases, 379,242 European ancestry controls NA Illumina [185301] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90084037 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W57: Bitten or stung by nonvenomous insect and other nonvenomous arthropods 549 European ancestry cases, 386,401 European ancestry controls NA Affymetrix, Illumina [509823] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081132 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73.0: Raynaud's syndrome (Gene-based burden) 1,538 European ancestry cases, 386,392 European ancestry controls NA Illumina [185344] 0 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90084035 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Nasal polyps 5,381 European ancestry cases, 381,522 European ancestry controls NA Affymetrix, Illumina [509820] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90081502 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I73.9: Peripheral vascular disease, unspecified (Gene-based burden) 3,601 European ancestry cases, 383,913 European ancestry controls NA Illumina [185341] 0 peripheral vascular disease http://www.ebi.ac.uk/efo/EFO_0003875 GCST90084036 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K57.9: Diverticular disease of intestine, part unspecified, without perforation or abscess 8,627 European ancestry cases, 378,304 European ancestry controls NA Affymetrix, Illumina [509817] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080248 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I74: Arterial embolism and thrombosis (Gene-based burden) 1,162 European ancestry cases, 386,633 European ancestry controls NA Illumina [185342] 0 arterial embolism, Arterial thrombosis http://www.ebi.ac.uk/efo/EFO_0010671, http://purl.obolibrary.org/obo/HP_0004420 GCST90084039 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R74.8: Abnormal levels of other serum enzymes 527 European ancestry cases, 386,424 European ancestry controls NA Affymetrix, Illumina [509816] 0 abnormality of serum enzyme levels http://www.ebi.ac.uk/efo/EFO_0009826 GCST90080907 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I74.3: Embolism and thrombosis of arteries of the lower extremities (Gene-based burden) 686 European ancestry cases, 387,213 European ancestry controls NA Illumina [185344] 0 arterial embolism, Arterial thrombosis http://www.ebi.ac.uk/efo/EFO_0010671, http://purl.obolibrary.org/obo/HP_0004420 GCST90084038 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H33: Retinal detachments and breaks 4,015 European ancestry cases, 382,918 European ancestry controls NA Affymetrix, Illumina [509810] 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90079897 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I77: Other disorders of arteries and arterioles (Gene-based burden) 1,882 European ancestry cases, 385,525 European ancestry controls NA Illumina [185338] 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90084041 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.0: Tachycardia, unspecified 3,250 European ancestry cases, 383,673 European ancestry controls NA Affymetrix, Illumina [509809] 0 Tachycardia http://purl.obolibrary.org/obo/HP_0001649 GCST90080750 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I77.1: Stricture of artery (Gene-based burden) 1,043 European ancestry cases, 386,876 European ancestry controls NA Illumina [185344] 0 stricture http://www.ebi.ac.uk/efo/EFO_0006818 GCST90084040 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S06: Intracranial injury 1,553 European ancestry cases, 385,423 European ancestry controls NA Affymetrix, Illumina [509809] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90080952 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I78: Diseases of capillaries (Gene-based burden) 934 European ancestry cases, 385,558 European ancestry controls NA Illumina [185322] 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90084043 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z37.9: Outcome of delivery, unspecified 863 European ancestry cases, 386,006 European ancestry controls NA Affymetrix, Illumina [509808] 0 birth measurement http://www.ebi.ac.uk/efo/EFO_0006921 GCST90081250 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I78.1: Nevus, non-neoplastic (Gene-based burden) 696 European ancestry cases, 387,219 European ancestry controls NA Illumina [185344] 0 nevus http://www.ebi.ac.uk/efo/EFO_0000625 GCST90084042 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S86: Injury of muscle, fascia and tendon at lower leg level 1,044 European ancestry cases, 385,884 European ancestry controls NA Affymetrix, Illumina [509807] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081033 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I80: Phlebitis and thrombophlebitis (Gene-based burden) 6,000 European ancestry cases, 378,260 European ancestry controls NA Illumina [185298] 0 Phlebitis, Thrombophlebitis http://www.ebi.ac.uk/efo/EFO_1001395, http://purl.obolibrary.org/obo/HP_0004418 GCST90084045 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G51: Facial nerve disorders 1,369 European ancestry cases, 385,508 European ancestry controls NA Affymetrix, Illumina [509793] 0 facial nerve disease http://www.ebi.ac.uk/efo/EFO_1002051 GCST90079839 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I80.2: Phlebitis and thrombophlebitis of other and unspecified deep vessels of lower extremities (Gene-based burden) 3,776 European ancestry cases, 383,943 European ancestry controls NA Illumina [185343] 0 Phlebitis, Thrombophlebitis http://www.ebi.ac.uk/efo/EFO_1001395, http://purl.obolibrary.org/obo/HP_0004418 GCST90084044 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M46: Other inflammatory spondylopathies 1,991 European ancestry cases, 384,956 European ancestry controls NA Affymetrix, Illumina [509781] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90080477 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82: Other venous embolism and thrombosis (Gene-based burden) 1,106 European ancestry cases, 385,404 European ancestry controls NA Illumina [185319] 0 venous thromboembolism http://www.ebi.ac.uk/efo/EFO_0004286 GCST90084049 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05.90: Thyrotoxicosis, unspecified without thyrotoxic crisis or storm 529 European ancestry cases, 386,362 European ancestry controls NA Affymetrix, Illumina [509776] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90079728 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82.4: Acute embolism and thrombosis of deep veins of lower extremity (Gene-based burden) 574 European ancestry cases, 386,116 European ancestry controls NA Illumina [185321] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90084048 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I34: Nonrheumatic mitral valve disorders 3,369 European ancestry cases, 383,491 European ancestry controls 4,769 European ancestry cases, 94,410 European ancestry controls Affymetrix, Illumina [509764] 0 mitral valve disease http://www.ebi.ac.uk/efo/EFO_0009557 GCST90079993 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82.40: Acute embolism and thrombosis of unspecified deep veins of lower extremity (Gene-based burden) 574 European ancestry cases, 386,116 European ancestry controls NA Illumina [185321] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90084047 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K42: Umbilical hernia 4,830 European ancestry cases, 382,071 European ancestry controls NA Affymetrix, Illumina [509764] 0 Umbilical hernia http://purl.obolibrary.org/obo/HP_0001537 GCST90080224 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I82.409.: Acute embolism and thrombosis of unspecified deep veins of unspecified lower extremity (Gene-based burden) 574 European ancestry cases, 386,116 European ancestry controls NA Illumina [185321] 0 deep vein thrombosis http://www.ebi.ac.uk/efo/EFO_0003907 GCST90084046 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.3: Stress incontinence (female) (male) 6,784 European ancestry cases, 380,112 European ancestry controls NA Affymetrix, Illumina [509762] 0 Stress urinary incontinence http://purl.obolibrary.org/obo/HP_0010992 GCST90080612 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83: Varicose veins of lower extremities (Gene-based burden) 15,125 European ancestry cases, 365,783 European ancestry controls NA Illumina [185231] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90084052 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.8: Other specified problems related to primary support group 610 European ancestry cases, 382,523 European ancestry controls NA Affymetrix, Illumina [506439] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081303 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.32: Other meniscus derangements, posterior horn of medial meniscus (Gene-based burden) 881 European ancestry cases, 387,049 European ancestry controls NA Illumina [185343] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084426 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17: Benign lipomatous neoplasm 8,433 European ancestry cases, 374,536 European ancestry controls NA Affymetrix, Illumina [506401] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90079669 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.33: Other meniscus derangements, other medial meniscus (Gene-based burden) 1,491 European ancestry cases, 386,439 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084427 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S99.9: Unspecified injury of ankle and foot 699 European ancestry cases, 382,202 European ancestry controls NA Affymetrix, Illumina [506380] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081044 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.36: Other meniscus derangements, other lateral meniscus (Gene-based burden) 671 European ancestry cases, 387,259 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084428 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E03: Other hypothyroidism 21,010 European ancestry cases, 362,055 European ancestry controls 25,043 European ancestry cases, 90,108 European ancestry controls Affymetrix, Illumina [506373] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90079722 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.4: Loose body in knee (Gene-based burden) 1,046 European ancestry cases, 386,884 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084430 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D50: Iron deficiency anemia 12,317 European ancestry cases, 370,728 European ancestry controls NA Affymetrix, Illumina [506358] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90079704 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.8: Other internal derangements of knee (Gene-based burden) 2,303 European ancestry cases, 385,622 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084432 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31: Hematuria 19,710 European ancestry cases, 363,299 European ancestry controls 13,283 European ancestry cases, 87,670 European ancestry controls Affymetrix, Illumina [506352] 1 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST90080842 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.81: Other internal derangements of knee (Gene-based burden) 600 European ancestry cases, 387,330 European ancestry controls NA Illumina [185341] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084431 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13: Other arthritis 17,422 European ancestry cases, 365,539 European ancestry controls NA Affymetrix, Illumina [506323] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90080405 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M24: Other specific joint derangements (Gene-based burden) 3,202 European ancestry cases, 383,964 European ancestry controls NA Illumina [185332] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90084436 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N18: Chronic kidney disease 10,144 European ancestry cases, 372,699 European ancestry controls 20,191 European ancestry cases, 99,375 European ancestry controls Affymetrix, Illumina [506308] 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90080584 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z83.3: Family history of diabetes mellitus 873 European ancestry cases, 382,547 European ancestry controls NA Affymetrix, Illumina [506680] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081340 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.94: Osteoarthritis, unspecified site (Gene-based burden) 1,597 European ancestry cases, 386,333 European ancestry controls NA Illumina [185344] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084409 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M53: Other and unspecified dorsopathies, not elsewhere classified 1,469 European ancestry cases, 382,067 European ancestry controls NA Affymetrix, Illumina [506679] 0 vertebral disorder http://purl.obolibrary.org/obo/MONDO_0045002 GCST90080499 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.97: Osteoarthritis, unspecified site (Gene-based burden) 3,143 European ancestry cases, 384,787 European ancestry controls NA Illumina [185344] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084410 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cirrhosis 1,995 European ancestry cases, 381,355 European ancestry controls NA Affymetrix, Illumina [506678] 1 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90081520 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.99: Osteoarthritis, unspecified site (Gene-based burden) 5,421 European ancestry cases, 382,509 European ancestry controls NA Illumina [185344] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084411 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.00: Insomnia, unspecified 1,539 European ancestry cases, 381,987 European ancestry controls NA Affymetrix, Illumina [506672] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90079831 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20: Acquired deformities of fingers and toes (Gene-based burden) 12,930 European ancestry cases, 368,891 European ancestry controls NA Illumina [185230] 0 congenital deformities of fingers http://purl.obolibrary.org/obo/MONDO_0017428 GCST90084418 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01.00: Unspecified blepharitis 1,280 European ancestry cases, 382,049 European ancestry controls NA Affymetrix, Illumina [506659] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90079865 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.1: Hallux valgus (acquired) (Gene-based burden) 7,729 European ancestry cases, 380,193 European ancestry controls NA Illumina [185344] 0 Hallux valgus http://purl.obolibrary.org/obo/HP_0001822 GCST90084414 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01.009.: Unspecified blepharitis unspecified eye, unspecified eyelid 1,280 European ancestry cases, 382,049 European ancestry controls NA Affymetrix, Illumina [506659] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90079864 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.2: Hallux rigidus (Gene-based burden) 1,822 European ancestry cases, 386,108 European ancestry controls NA Illumina [185344] 0 Hallux rigidus http://purl.obolibrary.org/obo/HP_0025004 GCST90084415 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L40: Psoriasis 5,629 European ancestry cases, 377,623 European ancestry controls 4,001 European ancestry cases, 118,929 European ancestry controls Affymetrix, Illumina [506651] 1 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90080349 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.4: Other hammer toe(s) (acquired) (Gene-based burden) 2,366 European ancestry cases, 385,393 European ancestry controls NA Illumina [185340] 0 Hammer Toe Syndrome http://www.ebi.ac.uk/efo/EFO_1001336 GCST90084416 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z09: Encounter for follow-up examination after completed treatment for conditions other than malignant neoplasm 18,227 European ancestry cases, 364,940 European ancestry controls NA Affymetrix, Illumina [506580] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081205 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20.5: Other deformities of toe(s) (acquired) (Gene-based burden) 2,079 European ancestry cases, 385,807 European ancestry controls NA Illumina [185344] 0 Abnormal foot morphology http://purl.obolibrary.org/obo/HP_0001760 GCST90084417 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.39: Personal history of other diseases of the musculoskeletal system and connective tissue 896 European ancestry cases, 382,287 European ancestry controls NA Affymetrix, Illumina [506580] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081370 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M22: Disorder of patella (Gene-based burden) 1,228 European ancestry cases, 384,932 European ancestry controls NA Illumina [185313] 0 disorder of patella http://www.ebi.ac.uk/efo/EFO_0009665 GCST90084419 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.21: Immunization not carried out because of patient refusal 1,818 European ancestry cases, 381,550 European ancestry controls NA Affymetrix, Illumina [506574] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081225 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23: Internal derangement of knee (Gene-based burden) 17,668 European ancestry cases, 368,598 European ancestry controls NA Illumina [185323] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084433 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L98.9: Disorder of the skin and subcutaneous tissue, unspecified 5,937 European ancestry cases, 377,141 European ancestry controls NA Affymetrix, Illumina [506560] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080383 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.2: Derangement of meniscus due to old tear or injury (Gene-based burden) 12,372 European ancestry cases, 375,533 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084424 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R35.0: Frequency of micturition 1,384 European ancestry cases, 381,947 European ancestry controls NA Affymetrix, Illumina [506546] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90080845 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23.20: Derangement of unspecified meniscus due to old tear or injury (Gene-based burden) 1,283 European ancestry cases, 386,609 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084420 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H90: Conductive and sensorineural hearing loss 1,841 European ancestry cases, 381,354 European ancestry controls NA Affymetrix, Illumina [506543] 0 sensorineural hearing loss http://www.ebi.ac.uk/efo/EFO_1001176 GCST90079946 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16.9: Osteoarthritis of hip, unspecified (Gene-based burden) 11,093 European ancestry cases, 376,837 European ancestry controls NA Illumina [185344] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90084397 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z91.0: Allergy status, other than to drugs and biological substances 5,096 European ancestry cases, 378,727 European ancestry controls NA Affymetrix, Illumina [506957] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081396 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17: Osteoarthritis of knee (Gene-based burden) 26,780 European ancestry cases, 354,384 European ancestry controls NA Illumina [185250] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90084402 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.2: Other abnormal auditory perceptions 1,176 European ancestry cases, 382,446 European ancestry controls NA Affymetrix, Illumina [506884] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90079956 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17.0: Bilateral primary osteoarthritis of knee (Gene-based burden) 1,430 European ancestry cases, 386,500 European ancestry controls NA Illumina [185344] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90084399 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.29: Other abnormal auditory perceptions 1,160 European ancestry cases, 382,463 European ancestry controls NA Affymetrix, Illumina [506884] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90079955 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17.1: Unilateral primary osteoarthritis of knee (Gene-based burden) 5,694 European ancestry cases, 381,977 European ancestry controls NA Illumina [185335] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90084400 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.299.: Other abnormal auditory perceptions, unspecified ear 1,160 European ancestry cases, 382,463 European ancestry controls NA Affymetrix, Illumina [506884] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90079954 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17.9: Osteoarthritis of knee, unspecified (Gene-based burden) 20,719 European ancestry cases, 364,237 European ancestry controls NA Illumina [185304] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90084401 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.09: Other abnormal glucose 1,839 European ancestry cases, 381,747 European ancestry controls NA Affymetrix, Illumina [506851] 0 Abnormal blood glucose concentration http://purl.obolibrary.org/obo/HP_0011015 GCST90080903 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M18: Osteoarthritis of first carpometacarpal joint (Gene-based burden) 1,788 European ancestry cases, 385,989 European ancestry controls NA Illumina [185340] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084404 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.81: Encounter for therapeutic drug level monitoring 6,041 European ancestry cases, 377,379 European ancestry controls NA Affymetrix, Illumina [506820] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081284 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M18.9: Osteoarthritis of first carpometacarpal joint, unspecified (Gene-based burden) 1,352 European ancestry cases, 386,578 European ancestry controls NA Illumina [185344] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084403 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M10: Gout 7,961 European ancestry cases, 375,561 European ancestry controls NA Affymetrix, Illumina [506814] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90080396 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19: Other and unspecified osteoarthritis (Gene-based burden) 29,459 European ancestry cases, 339,413 European ancestry controls NA Illumina [185075] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084413 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z51.8: Encounter for other specified aftercare 7,356 European ancestry cases, 376,032 European ancestry controls NA Affymetrix, Illumina [506784] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081285 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.0: Primary osteoarthritis of other joints (Gene-based burden) 1,787 European ancestry cases, 384,414 European ancestry controls NA Illumina [185317] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084406 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L73: Other follicular disorders 1,494 European ancestry cases, 381,939 European ancestry controls NA Affymetrix, Illumina [506780] 0 folliculitis http://www.ebi.ac.uk/efo/EFO_1000702 GCST90080366 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.07: Primary osteoarthritis ankle and foot (Gene-based burden) 604 European ancestry cases, 386,732 European ancestry controls NA Illumina [185333] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084405 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L25: Unspecified contact dermatitis 799 European ancestry cases, 382,796 European ancestry controls NA Affymetrix, Illumina [506739] 0 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90080339 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.9: Osteoarthritis, unspecified site (Gene-based burden) 23,959 European ancestry cases, 354,957 European ancestry controls NA Illumina [185223] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084412 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.09: Encounter for other general counseling and advice on contraception 3,230 European ancestry cases, 380,302 European ancestry controls NA Affymetrix, Illumina [506704] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081232 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.90: Unspecified osteoarthritis, unspecified site (Gene-based burden) 4,544 European ancestry cases, 372,887 European ancestry controls NA Illumina [185188] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084407 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H01.0: Blepharitis 1,881 European ancestry cases, 381,491 European ancestry controls NA Affymetrix, Illumina [506694] 0 blepharitis http://www.ebi.ac.uk/efo/EFO_0009536 GCST90079866 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.91: Primary osteoarthritis, unspecified site (Gene-based burden) 2,523 European ancestry cases, 385,407 European ancestry controls NA Illumina [185344] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90084408 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M24.1: Other articular cartilage disorders (Gene-based burden) 1,157 European ancestry cases, 386,756 European ancestry controls NA Illumina [185344] 0 articular cartilage of joint http://purl.obolibrary.org/obo/UBERON_0010996 GCST90084435 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R23: Other skin changes 1,606 European ancestry cases, 381,328 European ancestry controls NA Affymetrix, Illumina [506294] 0 Abnormality of the skin http://purl.obolibrary.org/obo/HP_0000951 GCST90080825 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M24.16: Other articular cartilage disorders (Gene-based burden) 605 European ancestry cases, 387,325 European ancestry controls NA Illumina [185344] 0 articular cartilage of joint http://purl.obolibrary.org/obo/UBERON_0010996 GCST90084434 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S99: Other and unspecified injuries of ankle and foot 737 European ancestry cases, 382,054 European ancestry controls NA Affymetrix, Illumina [506276] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081045 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25: Other joint disorder, not elsewhere classified (Gene-based burden) 46,051 European ancestry cases, 302,113 European ancestry controls NA Illumina [184626] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90084452 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.4: Personal history of diseases of genitourinary system 9,978 European ancestry cases, 373,090 European ancestry controls NA Affymetrix, Illumina [506275] 0 disease of genitourinary system http://www.ebi.ac.uk/efo/EFO_0009663 GCST90081373 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.4: Effusion of joint (Gene-based burden) 1,797 European ancestry cases, 385,607 European ancestry controls NA Illumina [185330] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90084438 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.82: Personal history of other (healed) physical injury and trauma 1,098 European ancestry cases, 381,734 European ancestry controls NA Affymetrix, Illumina [506225] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081376 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.46: Effusion, knee (Gene-based burden) 969 European ancestry cases, 386,961 European ancestry controls NA Illumina [185344] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90084437 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.828.: Personal history of other (healed) physical injury and trauma 1,098 European ancestry cases, 381,734 European ancestry controls NA Affymetrix, Illumina [506225] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081375 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.5: Pain in joint (Gene-based burden) 19,559 European ancestry cases, 348,462 European ancestry controls NA Illumina [184969] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90084446 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42: Fracture of shoulder and upper arm 3,861 European ancestry cases, 378,909 European ancestry controls NA Affymetrix, Illumina [506192] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080980 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.50: Pain in unspecified joint (Gene-based burden) 1,272 European ancestry cases, 383,393 European ancestry controls NA Illumina [185283] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90084439 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M76: Enthesopathies, lower limb, excluding foot 1,873 European ancestry cases, 380,906 European ancestry controls NA Affymetrix, Illumina [506186] 0 enthesopathy http://www.ebi.ac.uk/efo/EFO_0009666 GCST90080538 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.51: Pain in shoulder (Gene-based burden) 1,380 European ancestry cases, 386,550 European ancestry controls NA Illumina [185344] 0 Shoulder pain http://purl.obolibrary.org/obo/HP_0030834 GCST90084440 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R31.9: Hematuria, unspecified 2,270 European ancestry cases, 380,420 European ancestry controls NA Affymetrix, Illumina [506144] 0 Hematuria http://purl.obolibrary.org/obo/HP_0000790 GCST90080841 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.55: Pain in hip (Gene-based burden) 2,188 European ancestry cases, 385,742 European ancestry controls NA Illumina [185344] 0 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90084441 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80.9: Family history of malignant neoplasm, unspecified 740 European ancestry cases, 382,058 European ancestry controls NA Affymetrix, Illumina [506141] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90081333 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.56: Pain in knee (Gene-based burden) 11,057 European ancestry cases, 361,984 European ancestry controls NA Illumina [185054] 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90084443 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S13.4: Sprain of ligaments of cervical spine 993 European ancestry cases, 381,714 European ancestry controls NA Affymetrix, Illumina [506139] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080956 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.569.: Pain in unspecified knee (Gene-based burden) 8,703 European ancestry cases, 364,189 European ancestry controls NA Illumina [185051] 0 Knee pain http://purl.obolibrary.org/obo/HP_0030839 GCST90084442 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S13: Dislocation and sprain of joints and ligaments at neck level 1,078 European ancestry cases, 381,603 European ancestry controls NA Affymetrix, Illumina [506115] 0 neck injury http://www.ebi.ac.uk/efo/EFO_0009476 GCST90080957 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.57: Pain in ankle and joints of foot (Gene-based burden) 1,961 European ancestry cases, 382,634 European ancestry controls NA Illumina [185294] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90084445 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S89.9: Unspecified injury of lower leg 1,155 European ancestry cases, 381,371 European ancestry controls NA Affymetrix, Illumina [506096] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081035 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.571.: Pain in right ankle and joints of right foot (Gene-based burden) 988 European ancestry cases, 383,652 European ancestry controls NA Illumina [185298] 0 Arthralgia http://purl.obolibrary.org/obo/HP_0002829 GCST90084444 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - No Bipolar or Depression (UKB data field 20126) 74,867 European ancestry cases, 28,963 European ancestry controls NA Affymetrix, Illumina [191544] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90078308 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - Extremely (UKB data field 20497) (Gene-based burden) 914 European ancestry cases, 138,598 European ancestry controls NA Illumina [172118] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90082535 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Probable Recurrent major depression moderate (UKB data field 20126) 13,120 European ancestry cases, 90,710 European ancestry controls NA Affymetrix, Illumina [191544] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078312 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - Moderately (UKB data field 20497) (Gene-based burden) 5,330 European ancestry cases, 134,182 European ancestry controls NA Illumina [172118] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90082533 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Probable Recurrent major depression severe (UKB data field 20126) 7,594 European ancestry cases, 96,236 European ancestry controls NA Affymetrix, Illumina [191544] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078311 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Repeated disturbing thoughts of stressful experience in past month - Quite a bit (UKB data field 20497) (Gene-based burden) 3,952 European ancestry cases, 135,560 European ancestry controls NA Illumina [172118] 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90082534 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bipolar and major depression status - Single Probable major depression episode (UKB data field 20126) 6,953 European ancestry cases, 96,877 European ancestry controls NA Affymetrix, Illumina [191544] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90078313 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reproduciblity of spirometry measurement using ERS ATS criteria (UKB data field 20152) (Gene-based burden) 250,677 European ancestry cases, 71,325 European ancestry controls NA Illumina [183724] 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90082304 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power left (UKB data field 5119) 103,531 European ancestry individuals NA Affymetrix, Illumina [189272] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079297 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Restless during period of worst anxiety (UKB data field 20426) (Gene-based burden) 24,179 European ancestry cases, 16,027 European ancestry controls NA Illumina [135111] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90082429 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian angle left (UKB data field 5104) 103,531 European ancestry individuals NA Affymetrix, Illumina [189272] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079282 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Result ranking - third best i.e. worst (UKB data field 3059) (Gene-based burden) 298,624 European ancestry cases, 96,827 European ancestry controls NA Illumina [185485] 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90082997 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm strong meridian left (UKB data field 5135) 103,531 European ancestry individuals NA Affymetrix, Illumina [189272] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079301 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reticulocyte count (UKB data field 30250) (Gene-based burden) 412,501 European ancestry individuals NA Illumina [185680] 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90082987 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian angle left (UKB data field 5103) 103,531 European ancestry individuals NA Affymetrix, Illumina [189272] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079281 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Reticulocyte percentage (UKB data field 30240) (Gene-based burden) 412,501 European ancestry individuals NA Illumina [185680] 0 reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0010700 GCST90082986 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm weak meridian left (UKB data field 5096) 103,531 European ancestry individuals NA Affymetrix, Illumina [189272] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079273 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Risk taking (UKB data field 2040) (Gene-based burden) 113,078 European ancestry cases, 303,726 European ancestry controls NA Illumina [185730] 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90082404 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal power 103,531 European ancestry individuals NA Affymetrix, Illumina [189272] 1 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90081537 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 1 (UKB data field 21040) (Gene-based burden) 25,542 European ancestry cases, 128,881 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082752 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Corneal astigmatism 3mm left 103,531 European ancestry individuals NA Affymetrix, Illumina [189272] 0 Corneal astigmatism http://www.ebi.ac.uk/efo/EFO_1002040 GCST90081478 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 2 (UKB data field 21040) (Gene-based burden) 21,603 European ancestry cases, 132,820 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082753 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power angle left (UKB data field 5112) 103,515 European ancestry individuals NA Affymetrix, Illumina [189250] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079290 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Satisfaction with bowel habits - 3 (UKB data field 21040) (Gene-based burden) 12,583 European ancestry cases, 141,840 European ancestry controls NA Illumina [173973] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082754 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm cylindrical power right (UKB data field 5116) 103,540 European ancestry individuals NA Affymetrix, Illumina [189235] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079294 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index right (UKB data field 5160) 101,607 European ancestry individuals NA Affymetrix, Illumina [186196] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079315 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Bladder cancer (UKB data field 20001) (Gene-based burden) 1,128 European ancestry cases, 38,486 European ancestry controls NA Illumina [134284] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90081617 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry angle right (UKB data field 5108) 101,582 European ancestry individuals NA Affymetrix, Illumina [186160] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079286 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Breast cancer (UKB data field 20001) (Gene-based burden) 10,070 European ancestry cases, 29,544 European ancestry controls NA Illumina [134284] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90081612 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level right - doubtful (UKB data field 5152) 2,431 European ancestry cases, 99,151 European ancestry controls NA Affymetrix, Illumina [186160] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079306 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cervical cancer (UKB data field 20001) (Gene-based burden) 1,786 European ancestry cases, 37,828 European ancestry controls NA Illumina [134284] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90081620 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level right - high possibility abnormality (UKB data field 5152) 1,808 European ancestry cases, 99,774 European ancestry controls NA Affymetrix, Illumina [186160] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079307 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. CIN pre cancer cells cervix (UKB data field 20001) (Gene-based burden) 1,872 European ancestry cases, 37,742 European ancestry controls NA Illumina [134284] 0 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90081628 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level right - normal (UKB data field 5152) 99,565 European ancestry cases, 2,017 European ancestry controls NA Affymetrix, Illumina [186160] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079305 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Colon cancer / sigmoid cancer (UKB data field 20001) (Gene-based burden) 1,445 European ancestry cases, 38,169 European ancestry controls NA Illumina [134284] 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90081615 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index right (UKB data field 5159) 101,582 European ancestry individuals NA Affymetrix, Illumina [186160] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079314 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Kidney / renal cell cancer (UKB data field 20001) (Gene-based burden) 600 European ancestry cases, 39,014 European ancestry controls NA Illumina [134284] 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90081616 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index irregular astigmatism level left - doubtful (UKB data field 5149) 4,465 European ancestry cases, 96,853 European ancestry controls NA Affymetrix, Illumina [185843] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079303 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Large bowel cancer / colorectal cancer (UKB data field 20001) (Gene-based burden) 662 European ancestry cases, 38,952 European ancestry controls NA Illumina [134284] 0 colorectal carcinoma http://www.ebi.ac.uk/efo/EFO_1001951 GCST90081614 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index irregular astigmatism level left - high possibility abnormality (UKB data field 5149) 4,393 European ancestry cases, 96,925 European ancestry controls NA Affymetrix, Illumina [185843] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079304 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma (UKB data field 20001) (Gene-based burden) 3,595 European ancestry cases, 36,019 European ancestry controls NA Illumina [134284] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90081624 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index irregular astigmatism level left - normal (UKB data field 5149) 97,566 European ancestry cases, 3,752 European ancestry controls NA Affymetrix, Illumina [185843] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079302 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non hodgkins lymphoma (UKB data field 20001) (Gene-based burden) 885 European ancestry cases, 38,729 European ancestry controls NA Illumina [134284] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90081623 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm regularity index left (UKB data field 5163) 101,318 European ancestry individuals NA Affymetrix, Illumina [185843] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079318 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non melanoma skin cancer (UKB data field 20001) (Gene-based burden) 717 European ancestry cases, 38,897 European ancestry controls NA Illumina [134284] 0 non-melanoma skin carcinoma http://www.ebi.ac.uk/efo/EFO_0009260 GCST90081625 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry angle left (UKB data field 5111) 101,303 European ancestry individuals NA Affymetrix, Illumina [185823] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079289 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ovarian cancer (UKB data field 20001) (Gene-based burden) 769 European ancestry cases, 38,845 European ancestry controls NA Illumina [134284] 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90081618 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level left - doubtful (UKB data field 5155) 2,071 European ancestry cases, 99,232 European ancestry controls NA Affymetrix, Illumina [185823] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079309 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Prostate cancer (UKB data field 20001) (Gene-based burden) 3,622 European ancestry cases, 35,992 European ancestry controls NA Illumina [134265] 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90081621 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measure - 3mm asymmetry index irregular astigmatism level left - high possibility abnormality (UKB data field 5155) 1,659 European ancestry cases, 99,644 European ancestry controls NA Affymetrix, Illumina [185823] 0 eye measurement http://www.ebi.ac.uk/efo/EFO_0004731 GCST90079310 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - amitriptyline (Gene-based burden) 8,712 European ancestry cases, 312,046 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082075 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of esophagus (UKB data field 40006) 696 European ancestry cases, 73,534 European ancestry controls NA Affymetrix, Illumina [141236] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90079079 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - amlodipine (Gene-based burden) 19,689 European ancestry cases, 301,069 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082081 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of kidney, except renal pelvis (UKB data field 40006) 1,214 European ancestry cases, 73,016 European ancestry controls NA Affymetrix, Illumina [141236] 0 kidney neoplasm http://www.ebi.ac.uk/efo/EFO_0003865 GCST90079114 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - arimidex (Gene-based burden) 764 European ancestry cases, 319,994 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082145 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of lower lobe, bronchus or lung (UKB data field 40006) 626 European ancestry cases, 73,604 European ancestry controls NA Affymetrix, Illumina [141236] 0 lung neoplasm http://purl.obolibrary.org/obo/MONDO_0021117 GCST90079086 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - arthrotec (Gene-based burden) 612 European ancestry cases, 320,146 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082049 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of pancreas (UKB data field 40006) 682 European ancestry cases, 73,548 European ancestry controls NA Affymetrix, Illumina [141236] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90079084 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - asacol (Gene-based burden) 638 European ancestry cases, 320,120 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082017 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of rectum (UKB data field 40006) 1,566 European ancestry cases, 72,664 European ancestry controls NA Affymetrix, Illumina [141236] 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90079083 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - aspirin (Gene-based burden) 59,606 European ancestry cases, 261,152 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082030 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of sigmoid colon (UKB data field 40006) 1,290 European ancestry cases, 72,940 European ancestry controls NA Affymetrix, Illumina [141236] 0 sigmoid neoplasm http://www.ebi.ac.uk/efo/EFO_1001181 GCST90079081 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - aspirin (Gene-based burden) 2,789 European ancestry cases, 317,969 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081992 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of thyroid gland (UKB data field 40006) 546 European ancestry cases, 73,684 European ancestry controls NA Affymetrix, Illumina [141236] 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90079118 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - atenolol (Gene-based burden) 16,805 European ancestry cases, 303,953 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082025 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of unspecified part of bronchus or lung (UKB data field 40006) 558 European ancestry cases, 73,672 European ancestry controls NA Affymetrix, Illumina [141236] 0 lung neoplasm http://purl.obolibrary.org/obo/MONDO_0021117 GCST90079087 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - atorvastatin (Gene-based burden) 16,654 European ancestry cases, 304,104 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082164 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of upper lobe, bronchus or lung (UKB data field 40006) 1,142 European ancestry cases, 73,088 European ancestry controls NA Affymetrix, Illumina [141236] 0 lung neoplasm http://purl.obolibrary.org/obo/MONDO_0021117 GCST90079085 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - azathioprine (Gene-based burden) 928 European ancestry cases, 319,830 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082038 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Melanoma in situ (UKB data field 40006) 1,343 European ancestry cases, 72,887 European ancestry controls NA Affymetrix, Illumina [141236] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079126 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beclazone inhaler (Gene-based burden) 1,240 European ancestry cases, 319,518 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082002 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple myeloma (UKB data field 40006) 554 European ancestry cases, 73,676 European ancestry controls NA Affymetrix, Illumina [141236] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90079122 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beclometasone (Gene-based burden) 4,114 European ancestry cases, 316,644 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082124 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Multiple myeloma and malignant plasma cell neoplasms (UKB data field 40006) 609 European ancestry cases, 73,621 European ancestry controls NA Affymetrix, Illumina [141236] 0 multiple myeloma http://www.ebi.ac.uk/efo/EFO_0001378 GCST90079123 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beclomethasone (Gene-based burden) 1,802 European ancestry cases, 318,956 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082106 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neoplasm of uncertain behavior of bladder (UKB data field 40006) 799 European ancestry cases, 73,431 European ancestry controls NA Affymetrix, Illumina [141236] 0 bladder tumor http://www.ebi.ac.uk/efo/EFO_0000294 GCST90079135 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - beconase nasal spray (Gene-based burden) 3,080 European ancestry cases, 317,678 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082066 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Neoplasm of uncertain behavior of urinary organs (UKB data field 40006) 842 European ancestry cases, 73,388 European ancestry controls NA Affymetrix, Illumina [141236] 0 urinary system neoplasm http://purl.obolibrary.org/obo/MONDO_0021066 GCST90079136 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - becotide inhaler (Gene-based burden) 2,769 European ancestry cases, 317,989 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082001 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-follicular lymphoma (UKB data field 40006) 965 European ancestry cases, 73,265 European ancestry controls NA Affymetrix, Illumina [141236] 0 lymphoma http://www.ebi.ac.uk/efo/EFO_0000574 GCST90079120 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bendrofluazide (Gene-based burden) 2,528 European ancestry cases, 318,230 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082023 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin (UKB data field 40006) 21,805 European ancestry cases, 52,425 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079101 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bendroflumethiazide (Gene-based burden) 24,581 European ancestry cases, 296,177 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082216 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of ear and external auricular canal (UKB data field 40006) 667 European ancestry cases, 73,563 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079094 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - betahistine (Gene-based burden) 1,383 European ancestry cases, 319,375 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082119 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of eyelid, including canthus (UKB data field 40006) 887 European ancestry cases, 73,343 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079093 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - betamethasone (Gene-based burden) 727 European ancestry cases, 320,031 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082059 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of lower limb, including hip (UKB data field 40006) 1,080 European ancestry cases, 73,150 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079099 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - betnovate cream (Gene-based burden) 1,563 European ancestry cases, 319,195 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082089 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of parts of face (UKB data field 40006) 5,918 European ancestry cases, 68,312 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079095 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bisoprolol (Gene-based burden) 7,618 European ancestry cases, 313,140 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082077 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of scalp and neck (UKB data field 40006) 1,246 European ancestry cases, 72,984 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079096 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - bricanyl inhaler (Gene-based burden) 1,019 European ancestry cases, 319,739 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082000 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of trunk (UKB data field 40006) 2,568 European ancestry cases, 71,662 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079097 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - budesonide (Gene-based burden) 961 European ancestry cases, 319,797 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082003 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin of upper limb, including shoulder (UKB data field 40006) 1,381 European ancestry cases, 72,849 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079098 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcichew (Gene-based burden) 1,095 European ancestry cases, 319,663 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082044 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of skin, unspecified (UKB data field 40006) 8,504 European ancestry cases, 65,726 European ancestry controls NA Affymetrix, Illumina [141236] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079100 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - calcichew (Gene-based burden) 4,553 European ancestry cases, 316,205 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082047 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Non-Hodgkin lymphoma (UKB data field 40006) 504 European ancestry cases, 73,726 European ancestry controls NA Affymetrix, Illumina [141236] 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90079121 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Weekly (UKB data field 20413) 1,487 European ancestry cases, 75,056 European ancestry controls NA Affymetrix, Illumina [144451] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078424 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Severely (UKB data field 4814) (Gene-based burden) 1,664 European ancestry cases, 52,031 European ancestry controls NA Illumina [146068] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083210 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Daily or almost daily (UKB data field 20413) 653 European ancestry cases, 75,890 European ancestry controls NA Affymetrix, Illumina [144443] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078425 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Moderately (UKB data field 4814) (Gene-based burden) 8,948 European ancestry cases, 44,747 European ancestry controls NA Illumina [146068] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083211 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Thoughts of death during worst depression (UKB data field 20437) 38,829 European ancestry cases, 35,649 European ancestry controls NA Affymetrix, Illumina [141724] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078455 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Slightly (UKB data field 4814) (Gene-based burden) 26,815 European ancestry cases, 26,880 European ancestry controls NA Illumina [146068] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083212 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - About half of the day (UKB data field 20436) 10,425 European ancestry cases, 63,767 European ancestry controls NA Affymetrix, Illumina [141393] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078452 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Smokes on most or all days (UKB data field 22506) (Gene-based burden) 2,527 European ancestry cases, 105,181 European ancestry controls NA Illumina [165911] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082860 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - All day long (UKB data field 20436) 18,434 European ancestry cases, 55,758 European ancestry controls NA Affymetrix, Illumina [141393] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078454 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tobacco smoking - Occasionally (UKB data field 22506) (Gene-based burden) 1,697 European ancestry cases, 106,011 European ancestry controls NA Illumina [165911] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90082861 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fraction of day affected during worst episode of depression - Less than half of the day (UKB data field 20436) 9,562 European ancestry cases, 64,630 European ancestry controls NA Affymetrix, Illumina [141393] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078451 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trail making completion status - Timed out due to inactivity (UKB data field 20246) (Gene-based burden) 7,251 European ancestry cases, 99,849 European ancestry controls NA Illumina [166242] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082373 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of upper limb, including shoulder (UKB data field 40006) 825 European ancestry cases, 73,405 European ancestry controls NA Affymetrix, Illumina [141236] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079090 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - adalat (Gene-based burden) 1,019 European ancestry cases, 319,739 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081989 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of bladder (UKB data field 40006) 1,156 European ancestry cases, 73,074 European ancestry controls NA Affymetrix, Illumina [141236] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90079116 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - adcal (Gene-based burden) 1,512 European ancestry cases, 319,246 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082190 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of bladder, unspecified (UKB data field 40006) 965 European ancestry cases, 73,265 European ancestry controls NA Affymetrix, Illumina [141236] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90079115 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - adcal (Gene-based burden) 3,444 European ancestry cases, 317,314 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082179 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of brain (UKB data field 40006) 549 European ancestry cases, 73,681 European ancestry controls NA Affymetrix, Illumina [141236] 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90079117 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - alendronate sodium (Gene-based burden) 5,527 European ancestry cases, 315,231 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082142 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of bronchus and lung (UKB data field 40006) 2,464 European ancestry cases, 71,766 European ancestry controls NA Affymetrix, Illumina [141236] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90079088 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - alfuzosin (Gene-based burden) 1,052 European ancestry cases, 319,706 European ancestry controls NA Illumina [183807] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082078 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of cecum (UKB data field 40006) 648 European ancestry cases, 73,582 European ancestry controls NA Affymetrix, Illumina [141236] 0 cecal neoplasm http://www.ebi.ac.uk/efo/EFO_0009255 GCST90079080 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - allopurinol (Gene-based burden) 5,255 European ancestry cases, 315,503 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082063 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of colon (UKB data field 40006) 3,309 European ancestry cases, 70,921 European ancestry controls NA Affymetrix, Illumina [141236] 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90079082 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - close (UKB data field 20177) 720 European ancestry cases, 77,882 European ancestry controls NA Affymetrix, Illumina [148769] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078351 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Target heart rate achieved (UKB data field 6034) (Gene-based burden) 8,718 European ancestry cases, 71,794 European ancestry controls NA Illumina [159836] 0 achievement of target heart rate, self-reported http://www.ebi.ac.uk/efo/EFO_0009823 GCST90083406 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI7 synonym - pause (UKB data field 20177) 3,504 European ancestry cases, 75,098 European ancestry controls NA Affymetrix, Illumina [148769] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078350 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tea consumed (UKB data field 100390) (Gene-based burden) 155,356 European ancestry cases, 30,288 European ancestry controls NA Illumina [177616] 0 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST90081544 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Age at cancer diagnosis (UKB data field 40008) 78,689 European ancestry individuals NA Affymetrix, Illumina [148505] 0 age at diagnosis, cancer http://www.ebi.ac.uk/efo/EFO_0004918, http://purl.obolibrary.org/obo/MONDO_0004992 GCST90079137 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tea intake (UKB data field 1488) (Gene-based burden) 417,958 European ancestry individuals NA Illumina [185734] 0 tea consumption measurement http://www.ebi.ac.uk/efo/EFO_0010091 GCST90081573 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of depression (UKB data field 4609) 77,110 European ancestry individuals NA Affymetrix, Illumina [147062] 0 depressive episode measurement http://www.ebi.ac.uk/efo/EFO_0007704 GCST90079212 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tense / highly strung (UKB data field 1990) (Gene-based burden) 75,379 European ancestry cases, 342,726 European ancestry controls NA Illumina [185748] 0 feeling tense measurement http://www.ebi.ac.uk/efo/EFO_0009596 GCST90081611 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed days during worst episode of depression - Almost every day (UKB data field 20439) 39,262 European ancestry cases, 37,398 European ancestry controls NA Affymetrix, Illumina [145527] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078463 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tense, sore or aching muscles during worst period of anxiety (UKB data field 20417) (Gene-based burden) 15,553 European ancestry cases, 23,994 European ancestry controls NA Illumina [134527] 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90082423 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed days during worst episode of depression - Every day (UKB data field 20439) 29,547 European ancestry cases, 47,113 European ancestry controls NA Affymetrix, Illumina [145527] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078464 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Testosterone levels (UKB data field 30850) (Gene-based burden) 373,826 European ancestry individuals NA Illumina [185029] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90083028 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of depressed days during worst episode of depression - Less often (UKB data field 20439) 7,851 European ancestry cases, 68,809 European ancestry controls NA Affymetrix, Illumina [145527] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90078462 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Thoughts of death during worst depression (UKB data field 20437) (Gene-based burden) 38,829 European ancestry cases, 35,649 European ancestry controls NA Illumina [156243] 0 depressive symptom measurement http://www.ebi.ac.uk/efo/EFO_0007006 GCST90082441 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Behaviour of cancer tumour - Carcinoma in situ (UKB data field 40012) 12,102 European ancestry cases, 64,267 European ancestry controls NA Affymetrix, Illumina [144646] 0 in situ carcinoma http://purl.obolibrary.org/obo/MONDO_0004647 GCST90079139 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time since interview start at which blood pressure screens shown (UKB data field 96) (Gene-based burden) 430,929 European ancestry individuals NA Illumina [185950] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90083504 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Behaviour of cancer tumour - Malignant primary site (UKB data field 40012) 66,204 European ancestry cases, 10,165 European ancestry controls NA Affymetrix, Illumina [144646] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90079140 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time since last menstrual period (UKB data field 3700) (Gene-based burden) 46,881 European ancestry individuals NA Illumina [142611] 0 menstrual cycle measurement http://www.ebi.ac.uk/efo/EFO_0007786 GCST90083054 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Behaviour of cancer tumour - Benign (UKB data field 40012) 1,132 European ancestry cases, 75,236 European ancestry controls NA Affymetrix, Illumina [144645] 0 benign http://www.ebi.ac.uk/efo/EFO_0002751 GCST90079138 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - None (UKB data field 104900) (Gene-based burden) 132,094 European ancestry cases, 53,550 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081547 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of failure to fulfil normal expectations due to drinking alcohol in last year - Less than monthly (UKB data field 20407) 4,757 European ancestry cases, 71,885 European ancestry controls NA Affymetrix, Illumina [144627] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078407 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - Under 10 minutes (UKB data field 104900) (Gene-based burden) 49,933 European ancestry cases, 135,711 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081549 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of failure to fulfil normal expectations due to drinking alcohol in last year - Monthly (UKB data field 20407) 515 European ancestry cases, 76,127 European ancestry controls NA Affymetrix, Illumina [144627] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078408 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 10 to 30 minutes (UKB data field 104900) (Gene-based burden) 36,848 European ancestry cases, 148,796 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081548 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of failure to fulfil normal expectations due to drinking alcohol in last year - Never (UKB data field 20407) 71,066 European ancestry cases, 5,576 European ancestry controls NA Affymetrix, Illumina [144627] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078406 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 1 to 2 hours (UKB data field 104900) (Gene-based burden) 17,017 European ancestry cases, 168,627 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081550 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Less than monthly (UKB data field 20408) 8,452 European ancestry cases, 68,159 European ancestry controls NA Affymetrix, Illumina [144588] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078410 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 2 to 4 hours (UKB data field 104900) (Gene-based burden) 5,667 European ancestry cases, 179,977 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081551 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Monthly (UKB data field 20408) 1,315 European ancestry cases, 75,296 European ancestry controls NA Affymetrix, Illumina [144588] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078411 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 30 to 60 minutes (UKB data field 104900) (Gene-based burden) 31,516 European ancestry cases, 154,128 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081552 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Never (UKB data field 20408) 66,108 European ancestry cases, 10,503 European ancestry controls NA Affymetrix, Illumina [144588] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078409 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 4 to 6 hours (UKB data field 104900) (Gene-based burden) 1,470 European ancestry cases, 184,174 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081553 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of memory loss due to drinking alcohol in last year - Weekly (UKB data field 20408) 608 European ancestry cases, 76,003 European ancestry controls NA Affymetrix, Illumina [144588] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078412 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Time spent doing vigorous physical activity - 6+ hours (UKB data field 104900) (Gene-based burden) 543 European ancestry cases, 185,101 European ancestry controls NA Illumina [177616] 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90081554 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Daily or almost daily (UKB data field 20409) 590 European ancestry cases, 75,997 European ancestry controls NA Affymetrix, Illumina [144558] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078417 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching - Time to complete round (UKB data field 20133) (Gene-based burden) 102,772 European ancestry individuals NA Illumina [165118] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082300 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Less than monthly (UKB data field 20409) 10,792 European ancestry cases, 65,795 European ancestry controls NA Affymetrix, Illumina [144558] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078414 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Pairs matching - Time to complete round (UKB data field 400) (Gene-based burden) 423,480 European ancestry individuals NA Illumina [185828] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083127 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Monthly (UKB data field 20409) 2,026 European ancestry cases, 74,561 European ancestry controls NA Affymetrix, Illumina [144558] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078415 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Numeric memory - Time to complete test (UKB data field 4285) (Gene-based burden) 67,473 European ancestry individuals NA Illumina [152401] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083155 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Never (UKB data field 20409) 61,509 European ancestry cases, 15,078 European ancestry controls NA Affymetrix, Illumina [144558] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078413 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes now most or all of the time (UKB data field 4803) (Gene-based burden) 12,999 European ancestry cases, 161,792 European ancestry controls NA Illumina [176880] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083206 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Weekly (UKB data field 20409) 1,670 European ancestry cases, 74,917 European ancestry controls NA Affymetrix, Illumina [144558] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078416 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes now a lot of the time (UKB data field 4803) (Gene-based burden) 5,305 European ancestry cases, 169,486 European ancestry controls NA Illumina [176880] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083207 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Less than monthly (UKB data field 20413) 5,368 European ancestry cases, 71,175 European ancestry controls NA Affymetrix, Illumina [144451] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078422 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes now some of the time (UKB data field 4803) (Gene-based burden) 17,452 European ancestry cases, 157,339 European ancestry controls NA Illumina [176880] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083208 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Monthly (UKB data field 20413) 1,374 European ancestry cases, 75,169 European ancestry controls NA Affymetrix, Illumina [144451] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078423 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus - Yes but not now but have in the past (UKB data field 4803) (Gene-based burden) 20,407 European ancestry cases, 154,384 European ancestry controls NA Illumina [176880] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083209 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of inability to cease drinking in last year - Never (UKB data field 20413) 67,661 European ancestry cases, 8,882 European ancestry controls NA Affymetrix, Illumina [144451] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90078421 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Tinnitus severity nuisance - Not at all (UKB data field 4814) (Gene-based burden) 18,338 European ancestry cases, 35,357 European ancestry controls NA Illumina [146068] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083213 Exome-wide sequencing 2021-04-16 33773637 Traylor M 2021-03-25 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/33773637 Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies. Lacunar stroke 6,030 European ancestry cases, 248,929 European ancestry controls NA Illumina [6932927] (imputed) 5 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90014122 Genome-wide genotyping array 2021-04-16 33773637 Traylor M 2021-03-25 Lancet Neurol www.ncbi.nlm.nih.gov/pubmed/33773637 Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies. Lacunar stroke 7,338 European, African American, South Asian and Hispanic ancestry cases, 225,258 European, African American, South Asian and Hispanic ancestry controls NA Illumina [6922875] (imputed) 5 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90014123 Genome-wide genotyping array 2021-05-13 33836062 Kong XZ 2021-04-09 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/33836062 Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew. Brain asymmetrical skew (horizontal) 33,996 European ancestry individuals NA Affymetrix [9904141] (imputed) 1 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90017147 Genome-wide genotyping array 2021-05-13 33836062 Kong XZ 2021-04-09 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/33836062 Large-Scale Phenomic and Genomic Analysis of Brain Asymmetrical Skew. Brain asymmetrical skew (vertical) 33,996 European ancestry individuals NA Affymetrix [9904141] (imputed) 4 neuroimaging measurement http://www.ebi.ac.uk/efo/EFO_0004346 GCST90017148 Genome-wide genotyping array 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S20: Superficial injury of thorax 541 European ancestry cases, 386,810 European ancestry controls NA Affymetrix, Illumina [510195] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080958 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H83.0: Labyrinthitis (Gene-based burden) 897 European ancestry cases, 387,033 European ancestry controls NA Illumina [185344] 0 labyrinthitis http://www.ebi.ac.uk/efo/EFO_0009604 GCST90083930 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L98.8: Other specified disorders of the skin and subcutaneous tissue 1,157 European ancestry cases, 386,212 European ancestry controls NA Affymetrix, Illumina [510194] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080382 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H90: Conductive and sensorineural hearing loss (Gene-based burden) 1,841 European ancestry cases, 381,354 European ancestry controls NA Illumina [185289] 0 sensorineural hearing loss http://www.ebi.ac.uk/efo/EFO_1001176 GCST90083932 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z85: Personal history of malignant neoplasm 30,873 European ancestry cases, 356,515 European ancestry controls 15,719 European ancestry cases, 33,898 European ancestry controls Affymetrix, Illumina [510188] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90081354 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91: Other and unspecified hearing loss (Gene-based burden) 8,261 European ancestry cases, 363,853 European ancestry controls NA Illumina [185102] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90083937 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z74.0: Reduced mobility 500 European ancestry cases, 386,867 European ancestry controls NA Affymetrix, Illumina [510186] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081317 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.8: Other specified hearing loss (Gene-based burden) 1,017 European ancestry cases, 382,861 European ancestry controls NA Illumina [185290] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90083934 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96: Presence of other functional implants 24,749 European ancestry cases, 362,524 European ancestry controls NA Affymetrix, Illumina [510184] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081430 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.8X9.: Other specified hearing loss, unspecified ear (Gene-based burden) 940 European ancestry cases, 382,934 European ancestry controls NA Illumina [185290] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90083933 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81.0: Acute cholecystitis 1,074 European ancestry cases, 386,294 European ancestry controls NA Affymetrix, Illumina [510179] 0 Cholecystitis, Acute http://www.ebi.ac.uk/efo/EFO_1001289 GCST90080298 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.9: Unspecified hearing loss (Gene-based burden) 6,065 European ancestry cases, 374,041 European ancestry controls NA Illumina [185214] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90083936 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L53.9: Erythematous condition, unspecified 647 European ancestry cases, 386,732 European ancestry controls NA Affymetrix, Illumina [510178] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080353 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H91.90: Unspecified hearing loss, unspecified ear (Gene-based burden) 2,026 European ancestry cases, 377,733 European ancestry controls NA Illumina [185205] 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90083935 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R12: Heartburn 2,559 European ancestry cases, 384,798 European ancestry controls NA Affymetrix, Illumina [510177] 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90080797 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H92: Otalgia and effusion of ear (Gene-based burden) 4,717 European ancestry cases, 370,723 European ancestry controls NA Illumina [185135] 0 Ear pain, otitis media with effusion http://purl.obolibrary.org/obo/HP_0030766, http://www.ebi.ac.uk/efo/EFO_0007415 GCST90083938 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z96.1: Presence of intraocular lens 8,165 European ancestry cases, 379,112 European ancestry controls NA Affymetrix, Illumina [510174] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081427 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93: Other disorders of ear, not elsewhere classified (Gene-based burden) 4,651 European ancestry cases, 369,518 European ancestry controls NA Illumina [185100] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90083943 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56: Paralytic ileus and intestinal obstruction without hernia 5,258 European ancestry cases, 382,088 European ancestry controls NA Affymetrix, Illumina [510168] 0 Gastrointestinal obstruction http://purl.obolibrary.org/obo/HP_0004796 GCST90080244 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.1: Tinnitus (Gene-based burden) 963 European ancestry cases, 385,606 European ancestry controls NA Illumina [185328] 0 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90083939 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.07: Primary osteoarthritis ankle and foot 604 European ancestry cases, 386,732 European ancestry controls NA Affymetrix, Illumina [510168] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080419 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.2: Other abnormal auditory perceptions (Gene-based burden) 1,176 European ancestry cases, 382,446 European ancestry controls NA Illumina [185241] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90083942 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R40: Somnolence, stupor and coma 1,017 European ancestry cases, 386,284 European ancestry controls NA Affymetrix, Illumina [510161] 0 Coma http://purl.obolibrary.org/obo/HP_0001259 GCST90080853 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.29: Other abnormal auditory perceptions (Gene-based burden) 1,160 European ancestry cases, 382,463 European ancestry controls NA Illumina [185241] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90083941 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K31: Other diseases of stomach and duodenum 10,072 European ancestry cases, 377,247 European ancestry controls NA Affymetrix, Illumina [510154] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080213 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H65.3: Chronic mucoid otitis media (Gene-based burden) 732 European ancestry cases, 387,162 European ancestry controls NA Illumina [185342] 0 chronic otitis media http://purl.obolibrary.org/obo/MONDO_0021204 GCST90083917 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I87: Other disorders of veins 687 European ancestry cases, 386,724 European ancestry controls NA Affymetrix, Illumina [510239] 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90080078 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H66: Suppurative and unspecified otitis media (Gene-based burden) 3,333 European ancestry cases, 375,772 European ancestry controls NA Illumina [185197] 0 suppurative otitis media http://www.ebi.ac.uk/efo/EFO_0007503 GCST90083921 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J93: Pneumothorax and air leak 1,190 European ancestry cases, 386,185 European ancestry controls 547 European ancestry cases, 121,171 European ancestry controls Affymetrix, Illumina [510236] 0 pneumothorax http://purl.obolibrary.org/obo/MONDO_0002076 GCST90080153 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H66.9: Otitis media, unspecified (Gene-based burden) 1,110 European ancestry cases, 384,127 European ancestry controls NA Illumina [185303] 0 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST90083920 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W45: Foreign body or object entering through skin 648 European ancestry cases, 386,768 European ancestry controls NA Affymetrix, Illumina [510226] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081129 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H66.90: Otitis media, unspecified, unspecified ear (Gene-based burden) 553 European ancestry cases, 384,666 European ancestry controls NA Illumina [185303] 0 Otitis media http://www.ebi.ac.uk/efo/EFO_0004992 GCST90083919 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M25.4: Effusion of joint 1,797 European ancestry cases, 385,607 European ancestry controls NA Affymetrix, Illumina [510225] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90080452 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H69: Other and unspecified disorders of Eustachian tube (Gene-based burden) 1,569 European ancestry cases, 379,457 European ancestry controls NA Illumina [185200] 0 eustachian tube disease http://www.ebi.ac.uk/efo/EFO_0009667 GCST90083922 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J32.0: Chronic maxillary sinusitis 666 European ancestry cases, 386,725 European ancestry controls NA Affymetrix, Illumina [510222] 0 maxillary sinusitis http://www.ebi.ac.uk/efo/EFO_0007361 GCST90080107 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H71: Cholesteatoma of middle ear (Gene-based burden) 502 European ancestry cases, 387,301 European ancestry controls NA Illumina [31153] 0 cholesteatoma of middle ear http://www.ebi.ac.uk/efo/EFO_1000678 GCST90083923 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E10.9: Type 1 diabetes mellitus without complications 3,628 European ancestry cases, 383,813 European ancestry controls NA Affymetrix, Illumina [510215] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90079732 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H72: Perforation of tympanic membrane (Gene-based burden) 1,469 European ancestry cases, 385,072 European ancestry controls NA Illumina [185322] 0 tympanic membrane perforation http://www.ebi.ac.uk/efo/EFO_0009472 GCST90083925 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.1: Allergy status to other antibiotic agents status 4,694 European ancestry cases, 382,684 European ancestry controls NA Affymetrix, Illumina [510215] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081382 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H72.9: Unspecified perforation of tympanic membrane (Gene-based burden) 797 European ancestry cases, 387,027 European ancestry controls NA Illumina [185340] 0 tympanic membrane perforation http://www.ebi.ac.uk/efo/EFO_0009472 GCST90083924 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I77: Other disorders of arteries and arterioles 1,882 European ancestry cases, 385,525 European ancestry controls NA Affymetrix, Illumina [510214] 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90080055 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H73: Other disorders of tympanic membrane (Gene-based burden) 786 European ancestry cases, 385,979 European ancestry controls NA Illumina [185314] 0 tympanic membrane disease http://www.ebi.ac.uk/efo/EFO_0009570 GCST90083926 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I24: Other acute ischemic heart diseases 2,133 European ancestry cases, 385,287 European ancestry controls NA Affymetrix, Illumina [510212] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90079977 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H74: Other disorders of middle ear mastoid (Gene-based burden) 526 European ancestry cases, 387,108 European ancestry controls NA Illumina [185340] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90083927 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.2: Fracture of upper end of humerus 1,432 European ancestry cases, 385,935 European ancestry controls NA Affymetrix, Illumina [510211] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080977 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81: Disorders of vestibular function (Gene-based burden) 3,343 European ancestry cases, 378,017 European ancestry controls NA Illumina [185254] 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90083929 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53.1: Subjective visual disturbances 609 European ancestry cases, 386,755 European ancestry controls NA Affymetrix, Illumina [510206] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90079919 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81.0: Meniere's disease (Gene-based burden) 714 European ancestry cases, 387,216 European ancestry controls NA Illumina [185344] 0 Meniere disease http://www.ebi.ac.uk/efo/EFO_0006862 GCST90083928 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M77.4: Metatarsalgia 552 European ancestry cases, 386,812 European ancestry controls NA Affymetrix, Illumina [510204] 0 metatarsalgia http://www.ebi.ac.uk/efo/EFO_1001370 GCST90080540 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H83: Other diseases of inner ear (Gene-based burden) 2,745 European ancestry cases, 377,741 European ancestry controls NA Illumina [185231] 0 inner ear disease http://www.ebi.ac.uk/efo/EFO_0009672 GCST90083931 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Farsightedness - both eyes (UKB data field 5832) 23,800 European ancestry cases, 3,778 European ancestry controls NA Affymetrix, Illumina [58953] 0 hyperopia http://purl.obolibrary.org/obo/MONDO_0004891 GCST90079387 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of breast (UKB data field 40006) (Gene-based burden) 2,316 European ancestry cases, 38,689 European ancestry controls NA Illumina [135851] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90083115 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Farsightedness - left eye (UKB data field 5832) 1,912 European ancestry cases, 25,666 European ancestry controls NA Affymetrix, Illumina [58953] 0 hyperopia http://purl.obolibrary.org/obo/MONDO_0004891 GCST90079386 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of cervix uteri (UKB data field 40006) (Gene-based burden) 3,495 European ancestry cases, 37,510 European ancestry controls NA Illumina [135851] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90083117 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Farsightedness - right eye (UKB data field 5832) 2,102 European ancestry cases, 25,476 European ancestry controls NA Affymetrix, Illumina [58953] 0 hyperopia http://purl.obolibrary.org/obo/MONDO_0004891 GCST90079385 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of cervix, unspecified (UKB data field 40006) (Gene-based burden) 2,999 European ancestry cases, 38,006 European ancestry controls NA Illumina [135851] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90083116 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by menstrual cramps or other problems with period in the last three months - 602 Bothered a lot (UKB data field 21050) 905 European ancestry cases, 26,202 European ancestry controls NA Affymetrix, Illumina [57252] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078793 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of other and unspecified genital organs (UKB data field 40006) (Gene-based burden) 593 European ancestry cases, 73,637 European ancestry controls NA Illumina [155857] 0 urogenital neoplasm http://www.ebi.ac.uk/efo/EFO_0003863 GCST90083118 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by menstrual cramps or other problems with period in the last three months - Not bothered at all (UKB data field 21050) 22,936 European ancestry cases, 4,171 European ancestry controls NA Affymetrix, Illumina [57242] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078791 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of other and unspecified sites (UKB data field 40006) (Gene-based burden) 776 European ancestry cases, 73,454 European ancestry controls NA Illumina [155857] 0 carcinoma http://www.ebi.ac.uk/efo/EFO_0000313 GCST90083120 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by menstrual cramps or other problems with period in the last three months - 601 Bothered a little (UKB data field 21050) 3,266 European ancestry cases, 23,841 European ancestry controls NA Affymetrix, Illumina [57240] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90078792 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of skin (UKB data field 40006) (Gene-based burden) 1,322 European ancestry cases, 72,908 European ancestry controls NA Illumina [155857] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90083113 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes Neuropathy 751 European ancestry cases, 25,077 European ancestry controls NA Affymetrix, Illumina [55991] 0 type 2 diabetes nephropathy http://www.ebi.ac.uk/efo/EFO_0004997 GCST90081515 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronic lymphocytic leukemia of B-cell type (UKB data field 40006) (Gene-based burden) 571 European ancestry cases, 73,659 European ancestry controls NA Illumina [155857] 0 chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000095 GCST90083110 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes Ophthalmopathy 4,180 European ancestry cases, 21,737 European ancestry controls NA Affymetrix, Illumina [55965] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90081518 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diffuse large B-cell lymphoma (UKB data field 40006) (Gene-based burden) 672 European ancestry cases, 73,558 European ancestry controls NA Illumina [155857] 0 diffuse large B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000403 GCST90083105 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chest pain due to walking ceases when standing still (UKB data field 3616) 21,127 European ancestry cases, 4,846 European ancestry controls NA Affymetrix, Illumina [55886] 0 pain measurement http://www.ebi.ac.uk/efo/EFO_0010639 GCST90079067 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Intraductal carcinoma in situ of breast (UKB data field 40006) (Gene-based burden) 1,947 European ancestry cases, 39,058 European ancestry controls NA Illumina [135851] 0 Ductal Breast Carcinoma In Situ and Lobular Carcinoma In Situ http://www.ebi.ac.uk/efo/EFO_1000221 GCST90083114 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes Nephropathy Loose 2,067 European ancestry cases, 23,543 European ancestry controls NA Affymetrix, Illumina [55350] 0 type 2 diabetes nephropathy http://www.ebi.ac.uk/efo/EFO_0004997 GCST90081514 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Lymphoid leukemia (UKB data field 40006) (Gene-based burden) 699 European ancestry cases, 73,531 European ancestry controls NA Illumina [155857] 0 lymphoid leukemia http://www.ebi.ac.uk/efo/EFO_0004289 GCST90083111 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I needed less sleep than usual (UKB data field 20548) 4,681 European ancestry cases, 20,639 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078655 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of lower limb, including hip (UKB data field 40006) (Gene-based burden) 1,075 European ancestry cases, 73,155 European ancestry controls NA Illumina [155857] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083077 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was easily distracted (UKB data field 20548) 11,129 European ancestry cases, 14,191 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078657 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of skin (UKB data field 40006) (Gene-based burden) 3,349 European ancestry cases, 70,881 European ancestry controls NA Illumina [155857] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083078 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more active than usual (UKB data field 20548) 6,975 European ancestry cases, 18,345 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078659 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H93.299.: Other abnormal auditory perceptions, unspecified ear (Gene-based burden) 1,160 European ancestry cases, 382,463 European ancestry controls NA Illumina [185241] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90083940 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I34.0: Nonrheumatic mitral (valve) insufficiency 2,987 European ancestry cases, 384,345 European ancestry controls 4,104 European ancestry cases, 94,410 European ancestry controls Affymetrix, Illumina [510147] 0 mitral valve disease http://www.ebi.ac.uk/efo/EFO_0009557 GCST90079991 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08: Multiple valve diseases (Gene-based burden) 2,600 European ancestry cases, 385,228 European ancestry controls NA Illumina [185342] 0 heart valve disease http://www.ebi.ac.uk/efo/EFO_0009551 GCST90083947 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I45: Other conduction disorders 3,184 European ancestry cases, 384,091 European ancestry controls NA Affymetrix, Illumina [510141] 0 conduction system disorder http://www.ebi.ac.uk/efo/EFO_0005137 GCST90080007 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08.0: Rheumatic disorders of both mitral and aortic valves (Gene-based burden) 732 European ancestry cases, 387,198 European ancestry controls NA Illumina [185344] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90083944 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C43: Malignant melanoma of skin 2,807 European ancestry cases, 384,475 European ancestry controls 1,309 European ancestry cases, 117,531 European ancestry controls Affymetrix, Illumina [510134] 0 cutaneous melanoma http://www.ebi.ac.uk/efo/EFO_0000389 GCST90079593 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08.1: Rheumatic disorders of both mitral and tricuspid valves (Gene-based burden) 1,144 European ancestry cases, 386,786 European ancestry controls NA Illumina [185344] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90083945 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z60.2: Problems related to living alone 4,286 European ancestry cases, 383,078 European ancestry controls NA Affymetrix, Illumina [510134] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081298 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08.3: Combined rheumatic disorders of mitral, aortic and tricuspid valves (Gene-based burden) 608 European ancestry cases, 387,322 European ancestry controls NA Illumina [185344] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90083946 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.1: Cellulitis and acute lymphangitis of other parts of limb 7,078 European ancestry cases, 380,220 European ancestry controls NA Affymetrix, Illumina [510129] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90080328 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I10: Essential (primary) hypertension (Gene-based burden) 105,117 European ancestry cases, 269,090 European ancestry controls NA Illumina [185165] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90083948 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R56.8: Other and unspecified convulsions 2,538 European ancestry cases, 385,392 European ancestry controls NA Affymetrix, Illumina [510688] 0 Seizure http://purl.obolibrary.org/obo/HP_0001250 GCST90080881 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 25 (UKB data field 20179) (Gene-based burden) 8,154 European ancestry cases, 63,427 European ancestry controls NA Illumina [154207] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082339 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R61.9: Hyperhidrosis, unspecified 713 European ancestry cases, 387,217 European ancestry controls NA Affymetrix, Illumina [510688] 0 Hyperhidrosis http://purl.obolibrary.org/obo/HP_0000975 GCST90080891 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 26 (UKB data field 20179) (Gene-based burden) 54,304 European ancestry cases, 17,277 European ancestry controls NA Illumina [154207] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082340 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S02.20: Fracture of nasal bones 560 European ancestry cases, 387,370 European ancestry controls NA Affymetrix, Illumina [510688] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080945 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 27 (UKB data field 20179) (Gene-based burden) 4,127 European ancestry cases, 67,454 European ancestry controls NA Illumina [154207] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082341 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.30: Fracture of one rib 512 European ancestry cases, 387,418 European ancestry controls NA Affymetrix, Illumina [510688] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90080960 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 28 (UKB data field 20179) (Gene-based burden) 1,989 European ancestry cases, 69,592 European ancestry controls NA Illumina [154207] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082342 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.8: Open wound of other parts of wrist and hand (S61.8) 645 European ancestry cases, 387,285 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080995 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 29 (UKB data field 20179) (Gene-based burden) 3,007 European ancestry cases, 68,574 European ancestry controls NA Illumina [154207] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082343 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S61.9: Open wound of wrist and hand part, part unspecified (S61.9) 543 European ancestry cases, 387,387 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080996 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 25 (UKB data field 5012) (Gene-based burden) 12,040 European ancestry cases, 86,030 European ancestry controls NA Illumina [163501] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083246 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.80: Other fractures of lower leg 2,182 European ancestry cases, 385,748 European ancestry controls NA Affymetrix, Illumina [510688] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081025 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI8 chained arithmetic - 26 (UKB data field 5012) (Gene-based burden) 76,054 European ancestry cases, 22,016 European ancestry controls NA Illumina [163501] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083247 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of trunk (UKB data field 40006) (Gene-based burden) 1,039 European ancestry cases, 73,191 European ancestry controls NA Illumina [155857] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083075 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more confident than usual (UKB data field 20548) 4,064 European ancestry cases, 21,256 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078658 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant melanoma of upper limb, including shoulder (UKB data field 40006) (Gene-based burden) 825 European ancestry cases, 73,405 European ancestry controls NA Illumina [155857] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90083076 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more creative or had more ideas than usual (UKB data field 20548) 3,827 European ancestry cases, 21,493 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078656 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of bladder (UKB data field 40006) (Gene-based burden) 1,156 European ancestry cases, 73,074 European ancestry controls NA Illumina [155857] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90083102 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more restless than usual (UKB data field 20548) 15,465 European ancestry cases, 9,855 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078653 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of bladder, unspecified (UKB data field 40006) (Gene-based burden) 965 European ancestry cases, 73,265 European ancestry controls NA Illumina [155857] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90083101 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - I was more talkative than usual (UKB data field 20548) 6,709 European ancestry cases, 18,611 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078652 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of brain (UKB data field 40006) (Gene-based burden) 549 European ancestry cases, 73,681 European ancestry controls NA Illumina [155857] 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90083103 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manifestations of mania or irritability - My thoughts were racing (UKB data field 20548) 12,782 European ancestry cases, 12,538 European ancestry controls NA Affymetrix, Illumina [54031] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078654 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of breast (UKB data field 40006) (Gene-based burden) 12,472 European ancestry cases, 28,533 European ancestry controls NA Illumina [135851] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90083094 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 1 (UKB data field 6332) 8,910 European ancestry cases, 15,529 European ancestry controls NA Affymetrix, Illumina [53263] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079497 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of breast of unspecified site (UKB data field 40006) (Gene-based burden) 5,931 European ancestry cases, 35,074 European ancestry controls NA Illumina [135851] 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90083093 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 2 (UKB data field 6332) 23,214 European ancestry cases, 1,225 European ancestry controls NA Affymetrix, Illumina [53263] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079498 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of bronchus and lung (UKB data field 40006) (Gene-based burden) 2,464 European ancestry cases, 71,766 European ancestry controls NA Illumina [155857] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90083074 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Matrix pattern completion - Item selected for each puzzle - 4 (UKB data field 6332) 8,674 European ancestry cases, 15,765 European ancestry controls NA Affymetrix, Illumina [53263] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079499 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.3: Personal history of endocrine, nutritional and metabolic diseases 576 European ancestry cases, 386,857 European ancestry controls NA Affymetrix, Illumina [510249] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081358 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H60.9: Unspecified otitis externa (Gene-based burden) 1,675 European ancestry cases, 382,290 European ancestry controls NA Illumina [185287] 0 otitis externa http://www.ebi.ac.uk/efo/EFO_0009560 GCST90083914 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83: Other diseases of biliary tract 2,749 European ancestry cases, 384,669 European ancestry controls NA Affymetrix, Illumina [510246] 0 biliary tract disease http://www.ebi.ac.uk/efo/EFO_0009534 GCST90080308 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H60.90: Unspecified otitis externa, unspecified ear (Gene-based burden) 1,369 European ancestry cases, 382,576 European ancestry controls NA Illumina [185287] 0 otitis externa http://www.ebi.ac.uk/efo/EFO_0009560 GCST90083913 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82.8: Other fractures of lower leg 2,701 European ancestry cases, 384,726 European ancestry controls NA Affymetrix, Illumina [510246] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081026 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H61: Other disorders of external ear (Gene-based burden) 14,555 European ancestry cases, 355,834 European ancestry controls NA Illumina [185056] 0 external ear disease http://www.ebi.ac.uk/efo/EFO_0009668 GCST90083916 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I44: Atrioventricular and left bundle-branch block 5,320 European ancestry cases, 382,051 European ancestry controls NA Affymetrix, Illumina [510244] 0 bundle branch block http://www.ebi.ac.uk/efo/EFO_0004138 GCST90080005 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H65: Nonsuppurative otitis media (Gene-based burden) 1,877 European ancestry cases, 382,674 European ancestry controls NA Illumina [185287] 0 otitis media with effusion http://www.ebi.ac.uk/efo/EFO_0007415 GCST90083918 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J38: Diseases of vocal cords and larynx, not elsewhere classified 2,136 European ancestry cases, 385,278 European ancestry controls NA Affymetrix, Illumina [510241] 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90080122 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of mania or irritability - A week or more (UKB data field 20492) 7,805 European ancestry cases, 25,470 European ancestry controls NA Affymetrix, Illumina [69076] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078533 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin b6 preparation (Gene-based burden) 517 European ancestry cases, 320,241 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082126 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of mania or irritability - At least a day but less than a week (UKB data field 20492) 13,147 European ancestry cases, 20,128 European ancestry controls NA Affymetrix, Illumina [69076] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078532 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Longest period of mania or irritability - Less than 24 hours (UKB data field 20492) 12,323 European ancestry cases, 20,952 European ancestry controls NA Affymetrix, Illumina [69076] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90078531 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin c product (Gene-based burden) 5,639 European ancestry cases, 315,119 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082123 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin c product (Gene-based burden) 1,280 European ancestry cases, 319,478 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082222 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of problems due to mania or irritability - Needed treatment or caused problems with work relationships finances the law or other aspects of life (UKB data field 20493) 9,482 European ancestry cases, 22,464 European ancestry controls NA Affymetrix, Illumina [66494] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90078534 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin d product (Gene-based burden) 2,010 European ancestry cases, 318,748 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082045 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of manic irritable episodes - No problems (UKB data field 5674) 22,910 European ancestry cases, 8,213 European ancestry controls NA Affymetrix, Illumina [65578] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079370 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin e product (Gene-based burden) 1,685 European ancestry cases, 319,073 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082048 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of manic irritable episodes - Needed treatment or caused problems with work relationships finances the law or other aspects of life (UKB data field 5674) 8,512 European ancestry cases, 22,611 European ancestry controls NA Affymetrix, Illumina [65578] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079371 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - warfarin (Gene-based burden) 4,740 European ancestry cases, 316,018 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082109 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD SR: Ankylosing spondylitis - B27 positive 715 European ancestry cases, 30,652 European ancestry controls NA Affymetrix, Illumina [65540] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90079534 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - xalatan eye drops (Gene-based burden) 1,232 European ancestry cases, 319,526 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082163 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Fairly difficult (UKB data field 3476) 11,135 European ancestry cases, 19,862 European ancestry controls NA Affymetrix, Illumina [65407] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90079058 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - zinc product (Gene-based burden) 3,068 European ancestry cases, 317,690 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082113 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Fairly easy (UKB data field 3476) 6,721 European ancestry cases, 24,276 European ancestry controls NA Affymetrix, Illumina [65407] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90079057 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - zopiclone (Gene-based burden) 1,528 European ancestry cases, 319,230 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082007 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Very difficult (UKB data field 3476) 11,547 European ancestry cases, 19,450 European ancestry controls NA Affymetrix, Illumina [65407] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90079059 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Triglyceride levels (UKB data field 30870) (Gene-based burden) 411,757 European ancestry individuals NA Illumina [185663] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90083030 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty not smoking for 1 day - Very easy (UKB data field 3476) 1,994 European ancestry cases, 29,003 European ancestry controls NA Affymetrix, Illumina [65407] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90079056 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct left - abandon (UKB data field 4232) (Gene-based burden) 2,642 European ancestry cases, 170,293 European ancestry controls NA Illumina [176649] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90083151 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD M45: Ankylosing spondylitis - B27 positive 526 European ancestry cases, 30,652 European ancestry controls NA Affymetrix, Illumina [65200] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90079532 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct left - no (UKB data field 4232) (Gene-based burden) 171,828 European ancestry cases, 1,107 European ancestry controls NA Illumina [176649] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90083149 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Former alcohol drinker (UKB data field 3731) 15,969 European ancestry cases, 14,408 European ancestry controls NA Affymetrix, Illumina [64666] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90079069 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct left (UKB data field 4232) (Gene-based burden) 171,673 European ancestry cases, 1,262 European ancestry controls NA Illumina [176649] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90083150 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing loss noise exposure strict 16,069 European ancestry cases, 13,961 European ancestry controls NA Affymetrix, Illumina [63371] 0 noise-induced hearing loss http://www.ebi.ac.uk/efo/EFO_1001254 GCST90081540 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct right - abandon (UKB data field 4243) (Gene-based burden) 2,680 European ancestry cases, 170,241 European ancestry controls NA Illumina [176655] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90083154 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Every day (UKB data field 20454) 2,042 European ancestry cases, 27,933 European ancestry controls NA Affymetrix, Illumina [62608] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90078479 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct right - no (UKB data field 4243) (Gene-based burden) 171,830 European ancestry cases, 1,091 European ancestry controls NA Illumina [176655] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90083152 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Less than once a month (UKB data field 20454) 19,420 European ancestry cases, 10,555 European ancestry controls NA Affymetrix, Illumina [62608] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90078476 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Hearing test - Triplet correct right (UKB data field 4243) (Gene-based burden) 171,634 European ancestry cases, 1,287 European ancestry controls NA Illumina [176655] 0 hearing measurement http://www.ebi.ac.uk/efo/EFO_0007616 GCST90083153 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Once a month or more but not every week (UKB data field 20454) 3,579 European ancestry cases, 26,396 European ancestry controls NA Affymetrix, Illumina [62608] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90078477 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling asleep (UKB data field 20533) (Gene-based burden) 41,090 European ancestry cases, 13,020 European ancestry controls NA Illumina [146002] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90082601 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Maximum frequency of taking cannabis - Once a week or more but not every day (UKB data field 20454) 4,934 European ancestry cases, 25,041 European ancestry controls NA Affymetrix, Illumina [62608] 0 cannabis dependence measurement http://www.ebi.ac.uk/efo/EFO_0008457 GCST90078478 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling or staying asleep or sleeping too much - More than half the days (UKB data field 20517) (Gene-based burden) 10,002 European ancestry cases, 129,417 European ancestry controls NA Illumina [172110] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90082585 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Stronger worrying than other people during period of worst anxiety (UKB data field 20542) 24,579 European ancestry cases, 5,218 European ancestry controls NA Affymetrix, Illumina [62353] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90078633 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling or staying asleep or sleeping too much - Nearly every day (UKB data field 20517) (Gene-based burden) 11,208 European ancestry cases, 128,211 European ancestry controls NA Illumina [172110] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90082586 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - long (UKB data field 20181) 546 European ancestry cases, 28,784 European ancestry controls NA Affymetrix, Illumina [61668] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078358 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trouble falling or staying asleep or sleeping too much - Several days (UKB data field 20517) (Gene-based burden) 47,737 European ancestry cases, 91,682 European ancestry controls NA Illumina [172110] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90082584 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - metres (UKB data field 20181) 19,284 European ancestry cases, 10,046 European ancestry controls NA Affymetrix, Illumina [61668] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078359 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk fat free mass (UKB data field 23129) (Gene-based burden) 423,364 European ancestry individuals NA Illumina [185857] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90082918 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI9 concept interpolation - tall (UKB data field 20181) 9,336 European ancestry cases, 19,994 European ancestry controls NA Affymetrix, Illumina [61668] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90078360 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk fat mass (UKB data field 23128) (Gene-based burden) 423,433 European ancestry individuals NA Illumina [185858] 0 fat body mass http://www.ebi.ac.uk/efo/EFO_0005409 GCST90082917 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Length of longest manic irritable episode - At least two days but less than a week (UKB data field 5663) 17,754 European ancestry cases, 11,089 European ancestry controls NA Affymetrix, Illumina [61031] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079367 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk fat percentage (UKB data field 23127) (Gene-based burden) 423,451 European ancestry individuals NA Illumina [185858] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90082916 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Length of longest manic irritable episode - Less than a week (UKB data field 5663) 5,617 European ancestry cases, 23,226 European ancestry controls NA Affymetrix, Illumina [61031] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079368 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Trunk predicted mass (UKB data field 23130) (Gene-based burden) 423,325 European ancestry individuals NA Illumina [185857] 0 body weights and measures http://www.ebi.ac.uk/efo/EFO_0004324 GCST90082919 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Length of longest manic irritable episode - A week or more (UKB data field 5663) 6,072 European ancestry cases, 22,771 European ancestry controls NA Affymetrix, Illumina [61031] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079369 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Carcinoma in situ of bladder (UKB data field 40006) (Gene-based burden) 721 European ancestry cases, 73,509 European ancestry controls NA Illumina [155857] 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90083119 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tiotropium (Gene-based burden) 1,157 European ancestry cases, 319,601 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082204 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - None of the above (UKB data field 6156) 13,437 European ancestry cases, 21,996 European ancestry controls NA Affymetrix, Illumina [73806] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079477 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tolterodine left tartrate (Gene-based burden) 902 European ancestry cases, 319,856 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082176 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat depression - Other therapeutic activities such as mindfulness yoga or art classes (UKB data field 20547) 11,102 European ancestry cases, 24,529 European ancestry controls NA Affymetrix, Illumina [73282] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90078651 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tramadol (Gene-based burden) 4,956 European ancestry cases, 315,802 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082012 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Activities undertaken to treat depression - Talking therapies such as psychotherapy counselling group therapy or CBT (UKB data field 20547) 31,036 European ancestry cases, 4,595 European ancestry controls NA Affymetrix, Illumina [73282] 0 clinical treatment http://www.ebi.ac.uk/efo/EFO_0007056 GCST90078650 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tranexamic acid (Gene-based burden) 568 European ancestry cases, 320,190 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081993 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - effect of standing still - Pain usually continues for more than 10 minutes (UKB data field 5518) 13,520 European ancestry cases, 21,601 European ancestry controls NA Affymetrix, Illumina [73085] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079358 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - trazodone (Gene-based burden) 633 European ancestry cases, 320,125 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082076 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Leg pain on walking - effect of standing still - Pain usually disappears in less than 10 minutes (UKB data field 5518) 22,075 European ancestry cases, 13,046 European ancestry controls NA Affymetrix, Illumina [73085] 0 Lower limb pain http://purl.obolibrary.org/obo/HP_0012514 GCST90079359 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vagifem pessary (Gene-based burden) 1,431 European ancestry cases, 319,327 European ancestry controls NA Illumina [183952] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082032 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 92 (UKB data field 5699) 1,112 European ancestry cases, 32,967 European ancestry controls NA Affymetrix, Illumina [70927] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079372 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - valsartan (Gene-based burden) 2,102 European ancestry cases, 318,656 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082159 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 93 (UKB data field 5699) 2,325 European ancestry cases, 31,754 European ancestry controls NA Affymetrix, Illumina [70927] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079373 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - venlafaxine (Gene-based burden) 1,845 European ancestry cases, 318,913 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082135 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 94 (UKB data field 5699) 1,838 European ancestry cases, 32,241 European ancestry controls NA Affymetrix, Illumina [70927] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079374 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - ventolin inhaler (Gene-based burden) 13,099 European ancestry cases, 307,659 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081996 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 95 (UKB data field 5699) 27,553 European ancestry cases, 6,526 European ancestry controls NA Affymetrix, Illumina [70927] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079375 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - verapamil (Gene-based burden) 764 European ancestry cases, 319,994 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082112 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 96 (UKB data field 5699) 1,723 European ancestry cases, 32,356 European ancestry controls NA Affymetrix, Illumina [70927] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90079376 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - viscotears liquid eye gel (Gene-based burden) 1,058 European ancestry cases, 319,700 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082013 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of prostate (UKB data field 40006) 8,498 European ancestry cases, 24,727 European ancestry controls 3,139 European ancestry cases, 121,254 European ancestry controls Affymetrix, Illumina [69213] 1 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90079112 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin b compound (Gene-based burden) 3,325 European ancestry cases, 317,433 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082046 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Malignant neoplasm of testis (UKB data field 40006) 512 European ancestry cases, 32,713 European ancestry controls NA Affymetrix, Illumina [69213] 0 testicular carcinoma http://www.ebi.ac.uk/efo/EFO_0005088 GCST90079113 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - vitamin b12 preparation (Gene-based burden) 1,484 European ancestry cases, 319,274 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082042 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 3 (UKB data field 21039) 5,965 European ancestry cases, 29,976 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078757 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tamoxifen (Gene-based burden) 1,471 European ancestry cases, 319,287 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082039 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 4 (UKB data field 21039) 4,032 European ancestry cases, 31,909 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078758 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tamsulosin (Gene-based burden) 4,522 European ancestry cases, 316,236 European ancestry controls NA Illumina [183959] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082155 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 5 (UKB data field 21039) 5,472 European ancestry cases, 30,469 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078759 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tegretol (Gene-based burden) 952 European ancestry cases, 319,806 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082052 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 6 (UKB data field 21039) 3,970 European ancestry cases, 31,971 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078760 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - telmisartan (Gene-based burden) 698 European ancestry cases, 320,060 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082180 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 7 (UKB data field 21039) 3,790 European ancestry cases, 32,151 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078761 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - temazepam (Gene-based burden) 901 European ancestry cases, 319,857 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082009 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 8 (UKB data field 21039) 2,410 European ancestry cases, 33,531 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078762 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - terbinafine (Gene-based burden) 923 European ancestry cases, 319,835 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082156 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 9 (UKB data field 21039) 896 European ancestry cases, 35,045 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078763 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - terbutaline (Gene-based burden) 664 European ancestry cases, 320,094 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082080 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Severity of current abdominal distension tightness - 10 - Very severe distension (UKB data field 21039) 572 European ancestry cases, 35,369 European ancestry controls NA Affymetrix, Illumina [74146] 0 Abdominal distention http://purl.obolibrary.org/obo/HP_0003270 GCST90078754 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - thiamine preparation (Gene-based burden) 621 European ancestry cases, 320,137 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082110 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I was more active than usual (UKB data field 6156) 9,009 European ancestry cases, 26,424 European ancestry controls NA Affymetrix, Illumina [73806] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079472 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - thyroxine product (Gene-based burden) 5,384 European ancestry cases, 315,374 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082104 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I was more talkative than usual (UKB data field 6156) 7,538 European ancestry cases, 27,895 European ancestry controls NA Affymetrix, Illumina [73806] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079473 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - thyroxine sodium (Gene-based burden) 1,240 European ancestry cases, 319,518 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082060 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I needed less sleep than usual (UKB data field 6156) 4,907 European ancestry cases, 30,526 European ancestry controls NA Affymetrix, Illumina [73806] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079474 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tibolone (Gene-based burden) 768 European ancestry cases, 319,990 European ancestry controls NA Illumina [183964] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90082033 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - I was more creative or had more ideas than usual (UKB data field 6156) 4,295 European ancestry cases, 31,138 European ancestry controls NA Affymetrix, Illumina [73806] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079475 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Treatment or medication use - tildiem m/right tablet (Gene-based burden) 866 European ancestry cases, 319,892 European ancestry controls NA Illumina [183965] 0 drug use measurement http://www.ebi.ac.uk/efo/EFO_0007010 GCST90081990 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Manic hyper symptoms - All of the above (UKB data field 6156) 3,520 European ancestry cases, 31,913 European ancestry controls NA Affymetrix, Illumina [73806] 0 manic episode measurement http://www.ebi.ac.uk/efo/EFO_0007705 GCST90079476 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D13.1: Benign neoplasm of stomach (Gene-based burden) 1,028 European ancestry cases, 386,902 European ancestry controls NA Illumina [185344] 0 benign neoplasm of stomach http://purl.obolibrary.org/obo/MONDO_0021449 GCST90083649 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D41.4: Neoplasm of uncertain behavior of bladder 751 European ancestry cases, 387,179 European ancestry controls NA Affymetrix, Illumina [510619] 0 GCST90079697 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17: Benign lipomatous neoplasm (Gene-based burden) 8,433 European ancestry cases, 374,536 European ancestry controls NA Illumina [185291] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90083655 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K92.2: Gastrointestinal hemorrhage, unspecified 7,799 European ancestry cases, 380,066 European ancestry controls NA Affymetrix, Illumina [510617] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080321 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.0: Benign lipomatous neoplasm of skin and subcutaneous tissue of head, face and neck (Gene-based burden) 1,059 European ancestry cases, 386,871 European ancestry controls NA Illumina [185344] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90083651 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D10: Benign neoplasm of mouth and pharynx 554 European ancestry cases, 387,290 European ancestry controls NA Affymetrix, Illumina [510616] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079652 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.1: Benign lipomatous neoplasm of skin and subcutaneous tissue of trunk (Gene-based burden) 2,486 European ancestry cases, 385,444 European ancestry controls NA Illumina [185344] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90083652 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.9: Unspecified disorder of eyelid 856 European ancestry cases, 386,977 European ancestry controls NA Affymetrix, Illumina [510616] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90079873 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.2: Benign lipomatous neoplasm of skin and subcutaneous tissue of limb (Gene-based burden) 1,978 European ancestry cases, 385,952 European ancestry controls NA Illumina [185344] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90083653 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W31: Contact with other and unspecified machinery 564 European ancestry cases, 387,285 European ancestry controls NA Affymetrix, Illumina [510614] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081126 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.6: Benign lipomatous neoplasm of spermatic cord (Gene-based burden) 954 European ancestry cases, 193,651 European ancestry controls NA Illumina [177570] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90083654 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50.1: Cervical disc disorder with radiculopathy 642 European ancestry cases, 387,203 European ancestry controls NA Affymetrix, Illumina [510611] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90080492 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D18: Hemangioma and lymphangioma, any site (Gene-based burden) 2,097 European ancestry cases, 384,010 European ancestry controls NA Illumina [185316] 0 lymphangioma, hemangioma http://purl.obolibrary.org/obo/MONDO_0002013, http://www.ebi.ac.uk/efo/EFO_1000635 GCST90083657 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S27: Injury of other and unspecified intrathoracic organs 881 European ancestry cases, 386,963 European ancestry controls NA Affymetrix, Illumina [510610] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080964 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D18.0: Hemangioma (Gene-based burden) 1,813 European ancestry cases, 386,087 European ancestry controls NA Illumina [185344] 0 hemangioma http://www.ebi.ac.uk/efo/EFO_1000635 GCST90083656 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F00: Dementia in Alzheimer's disease 508 European ancestry cases, 387,422 European ancestry controls NA Affymetrix, Illumina [510609] 0 dementia http://purl.obolibrary.org/obo/MONDO_0001627 GCST90079783 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D21: Other benign neoplasms of connective and other soft tissue (Gene-based burden) 729 European ancestry cases, 386,265 European ancestry controls NA Illumina [185336] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083658 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.1: Pulmonary collapse 3,065 European ancestry cases, 384,755 European ancestry controls NA Affymetrix, Illumina [510609] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080158 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22: Melanocytic nevi (Gene-based burden) 7,622 European ancestry cases, 371,925 European ancestry controls NA Illumina [185206] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90083663 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K13.0: Diseases of lips 824 European ancestry cases, 387,005 European ancestry controls NA Affymetrix, Illumina [510608] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90080180 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.3: Melanocytic nevi of other and unspecified parts of face (Gene-based burden) 1,928 European ancestry cases, 386,001 European ancestry controls NA Illumina [185344] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90083659 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z98.1: Arthrodesis status 786 European ancestry cases, 387,058 European ancestry controls NA Affymetrix, Illumina [510608] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081436 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.5: Melanocytic nevi of trunk (Gene-based burden) 1,702 European ancestry cases, 386,228 European ancestry controls NA Illumina [185344] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90083660 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.3: Cellulitis and acute lymphangitis of trunk 764 European ancestry cases, 387,073 European ancestry controls NA Affymetrix, Illumina [510606] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90080329 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.6: Melanocytic nevi of upper limb, including shoulder (Gene-based burden) 592 European ancestry cases, 387,338 European ancestry controls NA Illumina [185344] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90083661 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78: Secondary malignant neoplasm of respiratory and digestive organs 6,526 European ancestry cases, 381,309 European ancestry controls 1,102 European ancestry cases, 121,574 European ancestry controls Affymetrix, Illumina [510604] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079625 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D22.7: Melanocytic nevi of lower limb, including hip (Gene-based burden) 729 European ancestry cases, 387,201 European ancestry controls NA Illumina [185344] 0 melanocytic nevus http://www.ebi.ac.uk/efo/EFO_0009675 GCST90083662 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H35.8: Other specified retinal disorders 1,101 European ancestry cases, 386,738 European ancestry controls NA Affymetrix, Illumina [510604] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90079901 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23: Other benign neoplasms of skin (Gene-based burden) 7,862 European ancestry cases, 369,330 European ancestry controls NA Illumina [185181] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083669 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.4: Dyskinesia of esophagus 629 European ancestry cases, 387,219 European ancestry controls NA Affymetrix, Illumina [510603] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90080191 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.1: Other benign neoplasm of skin of eyelid, including canthus (Gene-based burden) 1,342 European ancestry cases, 386,579 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083664 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N99: Intraoperative and postprocedural complications and disorders of genitourinary system, not elsewhere classified 1,366 European ancestry cases, 386,465 European ancestry controls NA Affymetrix, Illumina [510603] 0 disease of genitourinary system http://www.ebi.ac.uk/efo/EFO_0009663 GCST90080702 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.3: Other benign neoplasm of skin of other and unspecified parts of face (Gene-based burden) 824 European ancestry cases, 387,106 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083665 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.4: Ptosis of eyelid 1,655 European ancestry cases, 386,181 European ancestry controls NA Affymetrix, Illumina [510602] 0 ptosis http://purl.obolibrary.org/obo/MONDO_0000728 GCST90079871 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.5: Other benign neoplasm of skin of trunk (Gene-based burden) 765 European ancestry cases, 387,165 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083666 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I08: Multiple valve diseases 2,600 European ancestry cases, 385,228 European ancestry controls NA Affymetrix, Illumina [510600] 0 heart valve disease http://www.ebi.ac.uk/efo/EFO_0009551 GCST90079961 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.6: Other benign neoplasm of skin of upper limb, including shoulder (Gene-based burden) 601 European ancestry cases, 387,329 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083667 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I27: Other pulmonary heart diseases 1,249 European ancestry cases, 386,560 European ancestry controls NA Affymetrix, Illumina [510600] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90079987 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D23.7: Other benign neoplasm of skin of lower limb, including hip (Gene-based burden) 689 European ancestry cases, 387,241 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083668 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J81: Pulmonary edema 688 European ancestry cases, 387,127 European ancestry controls NA Affymetrix, Illumina [510600] 0 pulmonary edema http://www.ebi.ac.uk/efo/EFO_1001134 GCST90080145 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D24: Benign neoplasm of breast (Gene-based burden) 1,779 European ancestry cases, 208,433 European ancestry controls NA Illumina [179829] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083670 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K91: Intraoperative and postprocedural complications and disorders of digestive system, not elsewhere classified 2,050 European ancestry cases, 385,784 European ancestry controls 5,440 European ancestry cases, 110,222 European ancestry controls Affymetrix, Illumina [510600] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080318 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25: Leiomyoma of uterus (Gene-based burden) 11,770 European ancestry cases, 196,439 European ancestry controls NA Illumina [179695] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90083675 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F31.9: Bipolar disorder, unspecified 1,108 European ancestry cases, 386,721 European ancestry controls NA Affymetrix, Illumina [510599] 0 bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004985 GCST90079801 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.0: Submucous leiomyoma of uterus (Gene-based burden) 1,413 European ancestry cases, 227,721 European ancestry controls NA Illumina [180826] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90083671 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K55: Vascular disorders of intestine 1,491 European ancestry cases, 386,337 European ancestry controls NA Affymetrix, Illumina [510599] 0 vascular disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0004264, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080239 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.1: Intramural leiomyoma of uterus (Gene-based burden) 1,064 European ancestry cases, 228,070 European ancestry controls NA Illumina [180826] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90083672 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N17: Acute kidney failure 7,925 European ancestry cases, 379,873 European ancestry controls NA Affymetrix, Illumina [510598] 0 acute kidney failure http://purl.obolibrary.org/obo/MONDO_0002492 GCST90080580 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.2: Subserosal leiomyoma of uterus (Gene-based burden) 755 European ancestry cases, 228,379 European ancestry controls NA Illumina [180826] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90083673 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E87.2: Acidosis 1,660 European ancestry cases, 386,169 European ancestry controls NA Affymetrix, Illumina [510597] 0 acidosis http://www.ebi.ac.uk/efo/EFO_1000014 GCST90079775 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D05.9: Unspecified type of carcinoma in situ of breast (Gene-based burden) 1,072 European ancestry cases, 228,062 European ancestry controls NA Illumina [180826] 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90083633 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W17: Other fall from one level to another 757 European ancestry cases, 387,116 European ancestry controls NA Affymetrix, Illumina [510628] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081112 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D06: Carcinoma in situ of cervix uteri (Gene-based burden) 665 European ancestry cases, 210,614 European ancestry controls NA Illumina [179902] 0 uterine cervix carcinoma in situ http://purl.obolibrary.org/obo/MONDO_0042487 GCST90083636 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G31.9: Degenerative disease of nervous system, unspecified 569 European ancestry cases, 387,296 European ancestry controls NA Affymetrix, Illumina [510627] 0 neurodegenerative disease http://www.ebi.ac.uk/efo/EFO_0005772 GCST90079820 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D06.9: Carcinoma in situ of cervix, unspecified (Gene-based burden) 569 European ancestry cases, 228,565 European ancestry controls NA Illumina [180826] 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90083635 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z93: Artificial opening status 3,783 European ancestry cases, 384,080 European ancestry controls 1,670 European ancestry cases, 34,847 European ancestry controls Affymetrix, Illumina [510627] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081416 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D07: Carcinoma in situ of other and unspecified genital organs (Gene-based burden) 669 European ancestry cases, 386,937 European ancestry controls NA Illumina [185340] 0 urogenital neoplasm http://www.ebi.ac.uk/efo/EFO_0003863 GCST90083637 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z99.8: Dependence on other enabling machines and devices 635 European ancestry cases, 387,219 European ancestry controls NA Affymetrix, Illumina [510626] 0 dependence on enabling machines and devices http://www.ebi.ac.uk/efo/EFO_0020981 GCST90081444 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D10: Benign neoplasm of mouth and pharynx (Gene-based burden) 554 European ancestry cases, 387,290 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083638 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J84.1: Other interstitial pulmonary diseases with fibrosis 1,304 European ancestry cases, 386,553 European ancestry controls NA Affymetrix, Illumina [510625] 0 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90080146 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D11: Benign neoplasm of major salivary glands (Gene-based burden) 567 European ancestry cases, 387,293 European ancestry controls NA Illumina [185339] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083639 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M05.9: Rheumatoid arthritis with rheumatoid factor, unspecified 654 European ancestry cases, 387,206 European ancestry controls NA Affymetrix, Illumina [510624] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90080386 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12: Benign neoplasm of colon, rectum, anus and anal canal (Gene-based burden) 16,948 European ancestry cases, 370,732 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083648 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T39.1: Poisoning by, adverse effect of and underdosing of 4-Aminophenol derivatives 1,576 European ancestry cases, 386,288 European ancestry controls NA Affymetrix, Illumina [510624] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081048 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.0: Benign neoplasm of cecum (Gene-based burden) 2,533 European ancestry cases, 385,397 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083640 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z12.1: Encounter for screening for malignant neoplasm of intestinal tract 8,319 European ancestry cases, 379,548 European ancestry controls 43,337 European ancestry cases, 21,925 European ancestry controls Affymetrix, Illumina [510624] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081207 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.2: Benign neoplasm of ascending colon (Gene-based burden) 2,707 European ancestry cases, 385,223 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083641 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z90.4: Acquired absence of other specified parts of digestive tract 8,508 European ancestry cases, 379,347 European ancestry controls 5,168 European ancestry cases, 33,208 European ancestry controls Affymetrix, Illumina [510624] 0 digestive system surgery http://www.ebi.ac.uk/efo/EFO_0020979 GCST90081392 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Snoring (UKB data field 1210) 154,235 European ancestry cases, 248,326 European ancestry controls NA Affymetrix, Illumina [523486] 0 Snoring http://purl.obolibrary.org/obo/HP_0025267 GCST90077580 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by dizziness in the last three months - 600 Not bothered at all (UKB data field 21053) (Gene-based burden) 113,250 European ancestry cases, 41,873 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082786 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Past tobacco smoking - I have never smoked (UKB data field 1249) 171,084 European ancestry cases, 226,005 European ancestry controls NA Affymetrix, Illumina [518783] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90077586 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by dizziness in the last three months - 601 Bothered a little (UKB data field 21053) (Gene-based burden) 38,621 European ancestry cases, 116,502 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082787 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Past tobacco smoking - Smoked on most or all days (UKB data field 1249) 109,016 European ancestry cases, 288,073 European ancestry controls NA Affymetrix, Illumina [518783] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90077585 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by dizziness in the last three months - 602 Bothered a lot (UKB data field 21053) (Gene-based burden) 3,252 European ancestry cases, 151,871 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082788 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced expiratory volume in 1 second FEV1 (UKB data field 3063) 395,451 European ancestry individuals 25,470 European ancestry individuals Affymetrix, Illumina [518130] 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90079017 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.6: Secondary malignant neoplasm of retroperitoneum and peritoneum 1,833 European ancestry cases, 386,097 European ancestry controls 166 European ancestry cases, 121,574 European ancestry controls Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079623 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 5 (UKB data field 21041) (Gene-based burden) 9,405 European ancestry cases, 145,035 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082766 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.7: Secondary malignant neoplasm of liver and intrahepatic bile duct 3,748 European ancestry cases, 384,182 European ancestry controls 586 European ancestry cases, 121,574 European ancestry controls Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079624 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 6 (UKB data field 21041) (Gene-based burden) 5,517 European ancestry cases, 148,923 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082767 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79.3: Secondary malignant neoplasm of brain and cerebral meninges 1,145 European ancestry cases, 386,785 European ancestry controls NA Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079626 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 7 (UKB data field 21041) (Gene-based burden) 5,316 European ancestry cases, 149,124 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082768 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C79.5: Secondary malignant neoplasm of bone and bone marrow 3,104 European ancestry cases, 384,826 European ancestry controls 735 European ancestry cases, 121,433 European ancestry controls Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079627 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 8 (UKB data field 21041) (Gene-based burden) 3,520 European ancestry cases, 150,920 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082769 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C80.0: Disseminated malignant neoplasm, unspecified 570 European ancestry cases, 387,360 European ancestry controls NA Affymetrix, Illumina [510688] 0 GCST90079630 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 9 (UKB data field 21041) (Gene-based burden) 1,521 European ancestry cases, 152,919 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082770 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C83.3: Diffuse large B-cell lymphoma 768 European ancestry cases, 387,162 European ancestry controls NA Affymetrix, Illumina [510688] 0 diffuse large B-cell lymphoma http://www.ebi.ac.uk/efo/EFO_0000403 GCST90079634 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 10 - Completely (UKB data field 21041) (Gene-based burden) 1,399 European ancestry cases, 153,041 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082761 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.0: Benign neoplasm of cecum 2,533 European ancestry cases, 385,397 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079654 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression possibly related to childbirth (UKB data field 20445) (Gene-based burden) 5,752 European ancestry cases, 39,705 European ancestry controls NA Illumina [139723] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082452 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.2: Benign neoplasm of ascending colon 2,707 European ancestry cases, 385,223 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079655 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Depression possibly related to stressful or traumatic event (UKB data field 20447) (Gene-based burden) 57,607 European ancestry cases, 21,243 European ancestry controls NA Illumina [157986] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90082454 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.3: Benign neoplasm of transverse colon 3,544 European ancestry cases, 384,386 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079656 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Coeliac disease or gluten sensitivity (UKB data field 21068) (Gene-based burden) 2,911 European ancestry cases, 151,167 European ancestry controls NA Illumina [173913] 0 celiac disease http://www.ebi.ac.uk/efo/EFO_0001060 GCST90082818 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.4: Benign neoplasm of descending colon 2,107 European ancestry cases, 385,823 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079657 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diagnosed with life threatening illness - Never (UKB data field 20528) (Gene-based burden) 116,449 European ancestry cases, 22,727 European ancestry controls NA Illumina [172063] 0 normal http://purl.obolibrary.org/obo/PATO_0000461 GCST90082597 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.5: Benign neoplasm of sigmoid colon 6,667 European ancestry cases, 381,263 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079658 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diagnosed with life threatening illness but not in the last 12 months (UKB data field 20528) (Gene-based burden) 19,704 European ancestry cases, 119,472 European ancestry controls NA Illumina [172063] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90082598 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.6: Benign neoplasm of colon, unspecified 2,672 European ancestry cases, 385,258 European ancestry controls 10,585 European ancestry cases, 84,953 European ancestry controls Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079659 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diagnosed with life threatening illness within the last 12 months (UKB data field 20528) (Gene-based burden) 3,023 European ancestry cases, 136,153 European ancestry controls NA Illumina [172063] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90082599 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.7: Benign neoplasm of rectosigmoid junction 515 European ancestry cases, 387,415 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079660 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B37.0: Candidal stomatitis 1,312 European ancestry cases, 386,618 European ancestry controls NA Affymetrix, Illumina [510688] 0 stomatitis http://www.ebi.ac.uk/efo/EFO_0009688 GCST90079555 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by menstrual cramps or other problems with period in the last three months - 602 Bothered a lot (UKB data field 21050) (Gene-based burden) 905 European ancestry cases, 26,202 European ancestry controls NA Illumina [119632] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082779 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95.4: Other streptococcus as the cause of diseases classified elsewhere 830 European ancestry cases, 387,100 European ancestry controls NA Affymetrix, Illumina [510688] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079561 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by nausea in the last three months - 600 Not bothered at all (UKB data field 21059) (Gene-based burden) 131,651 European ancestry cases, 23,472 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082803 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B95.7: Other staphylococcus as the cause of diseases classified elsewhere 618 European ancestry cases, 387,312 European ancestry controls NA Affymetrix, Illumina [510688] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079563 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by nausea in the last three months - 601 Bothered a little (UKB data field 21059) (Gene-based burden) 21,760 European ancestry cases, 133,363 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082804 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B98: Other specified infectious agents as the cause of diseases classified to other chapters 1,560 European ancestry cases, 386,369 European ancestry controls NA Affymetrix, Illumina [510688] 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90079572 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by nausea in the last three months - 602 Bothered a lot (UKB data field 21059) (Gene-based burden) 1,712 European ancestry cases, 153,411 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082805 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 B98.0: Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters 1,559 European ancestry cases, 386,371 European ancestry controls NA Affymetrix, Illumina [510688] 0 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90079571 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain in arms legs joints in the past three months - 600 Not bothered at all (UKB data field 21049) (Gene-based burden) 42,914 European ancestry cases, 112,199 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082774 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C15.5: Malignant neoplasm of lower third of esophagus 556 European ancestry cases, 387,374 European ancestry controls NA Affymetrix, Illumina [510688] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90079573 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain in arms legs joints in the past three months - 601 Bothered a little (UKB data field 21049) (Gene-based burden) 79,690 European ancestry cases, 75,423 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082775 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C15.9: Malignant neoplasm of esophagus, unspecified 864 European ancestry cases, 387,066 European ancestry controls NA Affymetrix, Illumina [510688] 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90079574 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain in arms legs joints in the past three months - 602 Bothered a lot (UKB data field 21049) (Gene-based burden) 32,509 European ancestry cases, 122,604 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082776 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.0: Malignant neoplasm of cecum 774 European ancestry cases, 387,155 European ancestry controls 137 European ancestry cases, 122,068 European ancestry controls Affymetrix, Illumina [510688] 0 cecum cancer http://purl.obolibrary.org/obo/MONDO_0002033 GCST90079577 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain problems during intercourse in the last three months - 600 Not bothered at all (UKB data field 21057) (Gene-based burden) 81,222 European ancestry cases, 19,703 European ancestry controls NA Illumina [164190] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082797 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.2: Malignant neoplasm of ascending colon 549 European ancestry cases, 387,381 European ancestry controls NA Affymetrix, Illumina [510688] 0 colonic neoplasm http://www.ebi.ac.uk/efo/EFO_0004288 GCST90079578 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain problems during intercourse in the last three months - 601 Bothered a little (UKB data field 21057) (Gene-based burden) 14,178 European ancestry cases, 86,747 European ancestry controls NA Illumina [164190] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082798 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18.7: Malignant neoplasm of sigmoid colon 1,470 European ancestry cases, 386,460 European ancestry controls NA Affymetrix, Illumina [510688] 0 sigmoid neoplasm http://www.ebi.ac.uk/efo/EFO_1001181 GCST90079579 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by pain problems during intercourse in the last three months - 602 Bothered a lot (UKB data field 21057) (Gene-based burden) 5,525 European ancestry cases, 95,400 European ancestry controls NA Illumina [164190] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082799 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C25.9: Malignant neoplasm of pancreas, unspecified 872 European ancestry cases, 387,058 European ancestry controls NA Affymetrix, Illumina [510688] 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90079585 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by shortness of breath in the last three months - 600 Not bothered at all (UKB data field 21056) (Gene-based burden) 106,502 European ancestry cases, 48,638 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082794 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z46.6: Encounter for fitting and adjustment of urinary device 5,605 European ancestry cases, 382,323 European ancestry controls NA Affymetrix, Illumina [510688] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081265 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - 2 to 4 times a month (UKB data field 20414) (Gene-based burden) 25,530 European ancestry cases, 114,012 European ancestry controls NA Illumina [172128] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082414 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z47: Orthopedic aftercare 3,988 European ancestry cases, 383,942 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081268 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - 2 to 3 times a week (UKB data field 20414) (Gene-based burden) 41,974 European ancestry cases, 97,568 European ancestry controls NA Illumina [172128] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082415 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z47.0: Follow-up care involving removal of fracture plate and other internal fixation device 3,640 European ancestry cases, 384,290 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081267 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of drinking alcohol - 4 or more times a week (UKB data field 20414) (Gene-based burden) 42,676 European ancestry cases, 96,866 European ancestry controls NA Illumina [172128] 0 alcohol exposure measurement http://www.ebi.ac.uk/efo/EFO_0009113 GCST90082416 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50: Care involving use of rehabilitation procedures 5,250 European ancestry cases, 382,680 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081277 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of failure to fulfil normal expectations due to drinking alcohol in last year - Less than monthly (UKB data field 20407) (Gene-based burden) 4,757 European ancestry cases, 71,885 European ancestry controls NA Illumina [156129] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082393 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.0: Cardiac rehabilitation 686 European ancestry cases, 387,244 European ancestry controls NA Affymetrix, Illumina [510688] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081272 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of failure to fulfil normal expectations due to drinking alcohol in last year - Monthly (UKB data field 20407) (Gene-based burden) 515 European ancestry cases, 76,127 European ancestry controls NA Illumina [156129] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082394 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.1: Other physical therapy 2,855 European ancestry cases, 385,075 European ancestry controls NA Affymetrix, Illumina [510688] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081273 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of failure to fulfil normal expectations due to drinking alcohol in last year - Never (UKB data field 20407) (Gene-based burden) 71,066 European ancestry cases, 5,576 European ancestry controls NA Illumina [156129] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082392 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z50.7: Occupational therapy and vocational rehabilitation, not elsewhere classified 1,235 European ancestry cases, 386,695 European ancestry controls NA Affymetrix, Illumina [510688] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081274 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of feeling guilt or remorse after drinking alcohol in last year - Daily or almost daily (UKB data field 20409) (Gene-based burden) 590 European ancestry cases, 75,997 European ancestry controls NA Illumina [156091] 0 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90082403 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.3: Benign neoplasm of transverse colon (Gene-based burden) 3,544 European ancestry cases, 384,386 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083642 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.8: Other spondylosis 6,258 European ancestry cases, 381,603 European ancestry controls NA Affymetrix, Illumina [510622] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080482 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.4: Benign neoplasm of descending colon (Gene-based burden) 2,107 European ancestry cases, 385,823 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083643 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.0: Rheumatism, unspecified 1,093 European ancestry cases, 386,775 European ancestry controls NA Affymetrix, Illumina [510622] 0 rheumatic disease http://www.ebi.ac.uk/efo/EFO_0005755 GCST90080543 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.5: Benign neoplasm of sigmoid colon (Gene-based burden) 6,667 European ancestry cases, 381,263 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083644 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F20.9: Schizophrenia, unspecified 564 European ancestry cases, 387,292 European ancestry controls NA Affymetrix, Illumina [510621] 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90079799 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.6: Benign neoplasm of colon, unspecified (Gene-based burden) 2,672 European ancestry cases, 385,258 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083645 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W00: Fall due to ice and snow 1,315 European ancestry cases, 386,539 European ancestry controls NA Affymetrix, Illumina [510621] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081100 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.7: Benign neoplasm of rectosigmoid junction (Gene-based burden) 515 European ancestry cases, 387,415 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083646 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E27: Other disorders of adrenal gland 649 European ancestry cases, 387,197 European ancestry controls NA Affymetrix, Illumina [510620] 0 adrenal gland disease http://www.ebi.ac.uk/efo/EFO_0005539 GCST90079755 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.8: Benign neoplasm of rectum (Gene-based burden) 4,111 European ancestry cases, 383,819 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083647 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40.9: Epilepsy, unspecified 4,074 European ancestry cases, 383,779 European ancestry controls NA Affymetrix, Illumina [510620] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90079824 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D13: Benign neoplasm of other and ill-defined parts of digestive system (Gene-based burden) 1,532 European ancestry cases, 386,164 European ancestry controls NA Illumina [185342] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083650 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L90.5: Scar conditions and fibrosis of skin 2,723 European ancestry cases, 385,128 European ancestry controls NA Affymetrix, Illumina [510620] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080376 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diarrhoea when IBS symptoms first began (UKB data field 21074) (Gene-based burden) 9,581 European ancestry cases, 8,922 European ancestry controls NA Illumina [103177] 0 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST90082823 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12.8: Benign neoplasm of rectum 4,111 European ancestry cases, 383,819 European ancestry controls 420 European ancestry cases, 84,953 European ancestry controls Affymetrix, Illumina [510688] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079661 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diastolic blood pressure automated reading (UKB data field 4079) (Gene-based burden) 408,215 European ancestry individuals NA Illumina [185723] 0 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90083131 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D13.1: Benign neoplasm of stomach 1,028 European ancestry cases, 386,902 European ancestry controls 416 European ancestry cases, 101,962 European ancestry controls Affymetrix, Illumina [510688] 0 benign neoplasm of stomach http://purl.obolibrary.org/obo/MONDO_0021449 GCST90079663 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Sleep change (UKB data field 20532) (Gene-based burden) 54,110 European ancestry cases, 13,718 European ancestry controls NA Illumina [153551] 0 sleep measurement http://www.ebi.ac.uk/efo/EFO_0004870 GCST90082600 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.0: Benign lipomatous neoplasm of skin and subcutaneous tissue of head, face and neck 1,059 European ancestry cases, 386,871 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90079665 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Difficulty concentrating during worst depression (UKB data field 20435) (Gene-based burden) 54,939 European ancestry cases, 14,785 European ancestry controls NA Illumina [154219] 0 decreased concentration http://purl.obolibrary.org/obo/PATO_0001163 GCST90082436 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D17.1: Benign lipomatous neoplasm of skin and subcutaneous tissue of trunk 2,486 European ancestry cases, 385,444 European ancestry controls NA Affymetrix, Illumina [510688] 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90079666 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H72.9: Unspecified perforation of tympanic membrane 797 European ancestry cases, 387,027 European ancestry controls NA Affymetrix, Illumina [510597] 0 tympanic membrane perforation http://www.ebi.ac.uk/efo/EFO_0009472 GCST90079938 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D27: Benign neoplasm of ovary (Gene-based burden) 1,704 European ancestry cases, 210,162 European ancestry controls NA Illumina [179928] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083676 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z22.3: Carrier of other specified bacterial diseases 1,238 European ancestry cases, 386,591 European ancestry controls NA Affymetrix, Illumina [510597] 0 carrier status http://www.ebi.ac.uk/efo/EFO_0007658 GCST90081221 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D29: Benign neoplasm of male genital organs (Gene-based burden) 1,184 European ancestry cases, 172,279 European ancestry controls NA Illumina [175369] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083677 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I46.9: Cardiac arrest, cause unspecified 695 European ancestry cases, 387,131 European ancestry controls NA Affymetrix, Illumina [510595] 0 GCST90080009 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D32: Benign neoplasm of meninges (Gene-based burden) 651 European ancestry cases, 387,220 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083678 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S64: Injury of nerves at wrist and hand level 797 European ancestry cases, 387,028 European ancestry controls NA Affymetrix, Illumina [510595] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081004 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D35: Benign neoplasm of other and unspecified endocrine glands (Gene-based burden) 1,177 European ancestry cases, 386,605 European ancestry controls NA Illumina [185343] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083679 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W11: Fall on/from ladder 1,585 European ancestry cases, 386,260 European ancestry controls NA Affymetrix, Illumina [510595] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081111 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D36: Benign neoplasm of other and unspecified sites (Gene-based burden) 899 European ancestry cases, 386,761 European ancestry controls NA Illumina [185339] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083681 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.2: Allergy status to sulfonamides status 1,038 European ancestry cases, 386,819 European ancestry controls NA Affymetrix, Illumina [510595] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081383 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D36.1: Benign neoplasm of peripheral nerves and autonomic nervous system (Gene-based burden) 616 European ancestry cases, 387,313 European ancestry controls NA Illumina [185344] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90083680 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C91: Lymphoid leukemia 878 European ancestry cases, 386,951 European ancestry controls 457 European ancestry cases, 122,673 European ancestry controls Affymetrix, Illumina [510594] 1 lymphoid leukemia http://www.ebi.ac.uk/efo/EFO_0004289 GCST90079642 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D37: Neoplasm of uncertain behavior of oral cavity and digestive organs (Gene-based burden) 1,467 European ancestry cases, 386,363 European ancestry controls NA Illumina [185343] 0 GCST90083682 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T81.3: Disruption of wound, not elsewhere classified 1,668 European ancestry cases, 386,164 European ancestry controls NA Affymetrix, Illumina [510594] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081071 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D41: Neoplasm of uncertain behavior of urinary organs (Gene-based burden) 970 European ancestry cases, 386,931 European ancestry controls NA Illumina [185344] 0 GCST90083684 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D37: Neoplasm of uncertain behavior of oral cavity and digestive organs 1,467 European ancestry cases, 386,363 European ancestry controls NA Affymetrix, Illumina [510593] 0 GCST90079696 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by fainting spells in the last three months - 600 Not bothered at all (UKB data field 21054) (Gene-based burden) 150,281 European ancestry cases, 4,808 European ancestry controls NA Illumina [174057] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082789 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Forced vital capacity FVC (UKB data field 3062) 395,451 European ancestry individuals 25,470 European ancestry individuals Affymetrix, Illumina [518130] 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90079015 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by fainting spells in the last three months - 601 Bothered a little (UKB data field 21054) (Gene-based burden) 4,538 European ancestry cases, 150,551 European ancestry controls NA Illumina [174057] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082790 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Peak expiratory flow (UKB data field 3064) 395,451 European ancestry individuals NA Affymetrix, Illumina [518130] 1 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90079019 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling heart pound race in the last three months - 600 Not bothered at all (UKB data field 21055) (Gene-based burden) 107,650 European ancestry cases, 47,487 European ancestry controls NA Illumina [174059] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082791 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Result ranking - third best i.e. worst (UKB data field 3059) 298,624 European ancestry cases, 96,827 European ancestry controls NA Affymetrix, Illumina [518130] 0 pulmonary function measurement http://www.ebi.ac.uk/efo/EFO_0003892 GCST90079011 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling heart pound race in the last three months - 601 Bothered a little (UKB data field 21055) (Gene-based burden) 42,543 European ancestry cases, 112,594 European ancestry controls NA Illumina [174059] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082792 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Vitamin D levels (UKB data field 30890) 394,382 European ancestry individuals 56,282 European ancestry individuals Affymetrix, Illumina [516992] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90079047 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling heart pound race in the last three months - 602 Bothered a lot (UKB data field 21055) (Gene-based burden) 4,944 European ancestry cases, 150,193 European ancestry controls NA Illumina [174059] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082793 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - Definitely a morning person (UKB data field 1180) 107,453 European ancestry cases, 280,877 European ancestry controls NA Affymetrix, Illumina [511394] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90077573 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling tired all the time in the last three months - 600 Not bothered at all (UKB data field 21060) (Gene-based burden) 53,698 European ancestry cases, 101,431 European ancestry controls NA Illumina [174056] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082806 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - Definitely an evening person (UKB data field 1180) 36,316 European ancestry cases, 352,014 European ancestry controls NA Affymetrix, Illumina [511394] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90077576 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling tired all the time in the last three months - 601 Bothered a little (UKB data field 21060) (Gene-based burden) 76,420 European ancestry cases, 78,709 European ancestry controls NA Illumina [174056] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082807 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - More a morning than evening person (UKB data field 1180) 145,271 European ancestry cases, 243,059 European ancestry controls NA Affymetrix, Illumina [511394] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90077574 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by feeling tired all the time in the last three months - 602 Bothered a lot (UKB data field 21060) (Gene-based burden) 25,011 European ancestry cases, 130,118 European ancestry controls NA Illumina [174056] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082808 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Chronotype - More an evening than a morning person (UKB data field 1180) 114,330 European ancestry cases, 274,000 European ancestry controls NA Affymetrix, Illumina [511394] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90077575 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by headaches in the last three months - 600 Not bothered at all (UKB data field 21051) (Gene-based burden) 95,095 European ancestry cases, 60,063 European ancestry controls NA Illumina [174064] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082780 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A04.8: Other specified bacterial intestinal infections 1,799 European ancestry cases, 386,131 European ancestry controls NA Affymetrix, Illumina [510688] 0 intestinal infectious disease http://purl.obolibrary.org/obo/MONDO_0000916 GCST90079538 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by headaches in the last three months - 601 Bothered a little (UKB data field 21051) (Gene-based burden) 52,979 European ancestry cases, 102,179 European ancestry controls NA Illumina [174064] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082781 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A08.4: Viral intestinal infection, unspecified 910 European ancestry cases, 387,020 European ancestry controls NA Affymetrix, Illumina [510688] 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90079540 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by headaches in the last three months - 602 Bothered a lot (UKB data field 21051) (Gene-based burden) 7,084 European ancestry cases, 148,074 European ancestry controls NA Illumina [174064] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082782 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A09.9: Gastroenteritis and colitis of unspecified origin 8,538 European ancestry cases, 379,392 European ancestry controls NA Affymetrix, Illumina [510688] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90079542 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by menstrual cramps or other problems with period in the last three months - Not bothered at all (UKB data field 21050) (Gene-based burden) 22,936 European ancestry cases, 4,171 European ancestry controls NA Illumina [119612] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082777 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 A41.5: Sepsis due to other Gram-negative organisms 895 European ancestry cases, 387,035 European ancestry controls NA Affymetrix, Illumina [510688] 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90079544 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by menstrual cramps or other problems with period in the last three months - 601 Bothered a little (UKB data field 21050) (Gene-based burden) 3,266 European ancestry cases, 23,841 European ancestry controls NA Illumina [119630] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082778 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D25.9: Leiomyoma of uterus, unspecified (Gene-based burden) 8,919 European ancestry cases, 202,851 European ancestry controls NA Illumina [179932] 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90083674 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34.1: Malignant neoplasm of upper lobe, bronchus or lung 1,228 European ancestry cases, 386,702 European ancestry controls NA Affymetrix, Illumina [510688] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90079587 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by shortness of breath in the last three months - 601 Bothered a little (UKB data field 21056) (Gene-based burden) 42,621 European ancestry cases, 112,519 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082795 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C34.3: Malignant neoplasm of lower lobe, bronchus or lung 695 European ancestry cases, 387,235 European ancestry controls NA Affymetrix, Illumina [510688] 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90079588 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by shortness of breath in the last three months - 602 Bothered a lot (UKB data field 21056) (Gene-based burden) 6,017 European ancestry cases, 149,123 European ancestry controls NA Illumina [174061] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082796 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C43.6: Malignant melanoma of upper limb, including shoulder 614 European ancestry cases, 387,316 European ancestry controls NA Affymetrix, Illumina [510688] 0 melanoma http://www.ebi.ac.uk/efo/EFO_0000756 GCST90079591 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by trouble sleeping in the last three months - 600 Not bothered at all (UKB data field 21061) (Gene-based burden) 52,659 European ancestry cases, 102,465 European ancestry controls NA Illumina [174051] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082809 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.1: Other and unspecified malignant neoplasm of skin of eyelid, including canthus 1,565 European ancestry cases, 386,363 European ancestry controls NA Affymetrix, Illumina [510688] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079594 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by trouble sleeping in the last three months - 601 Bothered a little (UKB data field 21061) (Gene-based burden) 75,649 European ancestry cases, 79,475 European ancestry controls NA Illumina [174051] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082810 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.2: Other and unspecified malignant neoplasm of skin of ear and external auricular canal 1,075 European ancestry cases, 386,855 European ancestry controls NA Affymetrix, Illumina [510688] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079595 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by trouble sleeping in the last three months - 602 Bothered a lot (UKB data field 21061) (Gene-based burden) 26,816 European ancestry cases, 128,308 European ancestry controls NA Illumina [174051] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082811 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C44.3: Other and unspecified malignant neoplasm of skin of other and unspecified parts of face 7,572 European ancestry cases, 380,358 European ancestry controls 3,111 European ancestry cases, 113,204 European ancestry controls Affymetrix, Illumina [510688] 0 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90079596 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by urinary frequency bladder irritability in the last three months - 600 Not bothered at all (UKB data field 21058) (Gene-based burden) 85,424 European ancestry cases, 69,620 European ancestry controls NA Illumina [174046] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082800 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.0: Secondary and unspecified malignant neoplasm of lymph nodes of head, face and neck 933 European ancestry cases, 386,997 European ancestry controls NA Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079615 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by urinary frequency bladder irritability in the last three months - 601 Bothered a little (UKB data field 21058) (Gene-based burden) 51,192 European ancestry cases, 103,852 European ancestry controls NA Illumina [174046] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082801 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.1: Secondary and unspecified malignant neoplasm of intrathoracic lymph nodes 1,267 European ancestry cases, 386,663 European ancestry controls NA Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079616 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree bothered by urinary frequency bladder irritability in the last three months - 602 Bothered a lot (UKB data field 21058) (Gene-based burden) 18,428 European ancestry cases, 136,616 European ancestry controls NA Illumina [174046] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082802 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.2: Secondary and unspecified malignant neoplasm of intra-abdominal lymph nodes 1,880 European ancestry cases, 386,050 European ancestry controls NA Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079617 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 1 (UKB data field 21041) (Gene-based burden) 25,550 European ancestry cases, 128,890 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082762 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C77.3: Secondary and unspecified malignant neoplasm of axilla and upper limb lymph nodes 2,725 European ancestry cases, 385,205 European ancestry controls 177 European ancestry cases, 121,325 European ancestry controls Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079618 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 2 (UKB data field 21041) (Gene-based burden) 14,163 European ancestry cases, 140,277 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082763 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.0: Secondary malignant neoplasm of lung 2,742 European ancestry cases, 385,188 European ancestry controls NA Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079621 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 3 (UKB data field 21041) (Gene-based burden) 8,434 European ancestry cases, 146,006 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082764 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C78.2: Secondary malignant neoplasm of pleura 815 European ancestry cases, 387,115 European ancestry controls NA Affymetrix, Illumina [510688] 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90079622 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Degree to which abdominal pain discomfort altered bowel habits affect interfere with life in general - 4 (UKB data field 21041) (Gene-based burden) 4,573 European ancestry cases, 149,867 European ancestry controls NA Illumina [173965] 0 health satisfaction measurement http://www.ebi.ac.uk/efo/EFO_0009724 GCST90082765 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.0: Anal polyp 1,480 European ancestry cases, 386,450 European ancestry controls NA Affymetrix, Illumina [510688] 0 anal polyp http://purl.obolibrary.org/obo/MONDO_0060766 GCST90080262 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - A little bit (UKB data field 20496) (Gene-based burden) 18,130 European ancestry cases, 44,686 European ancestry controls NA Illumina [151343] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082528 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.3: Rectal prolapse 1,292 European ancestry cases, 386,638 European ancestry controls NA Affymetrix, Illumina [510688] 0 Rectal prolapse http://purl.obolibrary.org/obo/HP_0002035 GCST90080264 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - Extremely (UKB data field 20496) (Gene-based burden) 1,009 European ancestry cases, 61,807 European ancestry controls NA Illumina [151343] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082531 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K62.6: Ulcer of anus and rectum 528 European ancestry cases, 387,402 European ancestry controls NA Affymetrix, Illumina [510688] 0 anus disease http://www.ebi.ac.uk/efo/EFO_0009660 GCST90080266 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - Moderately (UKB data field 20496) (Gene-based burden) 4,193 European ancestry cases, 58,623 European ancestry controls NA Illumina [151343] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082529 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64.0: First degree hemorrhoids 577 European ancestry cases, 387,353 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080275 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt distant from other people in past month - Quite a bit (UKB data field 20496) (Gene-based burden) 3,396 European ancestry cases, 59,420 European ancestry controls NA Illumina [151343] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082530 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 501 Sometimes (UKB data field 21032) (Gene-based burden) 30,246 European ancestry cases, 52,900 European ancestry controls NA Illumina [159641] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082704 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.1: Personal history of long-term (current) use of anticoagulants 15,024 European ancestry cases, 372,906 European ancestry controls NA Affymetrix, Illumina [510688] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081404 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Frequency of harder stools when abdominal discomfort pain started - 502 Often (UKB data field 21032) (Gene-based burden) 5,831 European ancestry cases, 77,315 European ancestry controls NA Illumina [159641] 0 Abnormal stool composition http://purl.obolibrary.org/obo/HP_0031685 GCST90082705 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K37: Unspecified appendicitis 543 European ancestry cases, 387,117 European ancestry controls NA Affymetrix, Illumina [510471] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90080217 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40.9: Epilepsy, unspecified (Gene-based burden) 4,074 European ancestry cases, 383,779 European ancestry controls NA Illumina [185333] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90083810 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.5: Personal history of mental and behavioral disorders 1,209 European ancestry cases, 386,498 European ancestry controls NA Affymetrix, Illumina [510471] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90081360 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G43: Migraine (Gene-based burden) 8,426 European ancestry cases, 369,746 European ancestry controls NA Illumina [185182] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90083813 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J43: Emphysema 2,522 European ancestry cases, 385,122 European ancestry controls NA Affymetrix, Illumina [510470] 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90080128 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G43.9: Migraine, unspecified (Gene-based burden) 3,383 European ancestry cases, 384,515 European ancestry controls NA Illumina [185344] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90083812 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 C18: Malignant neoplasm of colon 3,899 European ancestry cases, 383,758 European ancestry controls 1,314 European ancestry cases, 122,068 European ancestry controls Affymetrix, Illumina [510466] 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90079581 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G44: Other headache syndromes (Gene-based burden) 1,382 European ancestry cases, 383,155 European ancestry controls NA Illumina [185261] 0 headache disorder http://www.ebi.ac.uk/efo/EFO_0009550 GCST90083814 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17.1: Unilateral primary osteoarthritis of knee 5,694 European ancestry cases, 381,977 European ancestry controls NA Affymetrix, Illumina [510463] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90080414 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G45: Transient cerebral ischemic attacks and related syndromes (Gene-based burden) 4,034 European ancestry cases, 381,709 European ancestry controls NA Illumina [185311] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90083816 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H74: Other disorders of middle ear mastoid 526 European ancestry cases, 387,108 European ancestry controls NA Affymetrix, Illumina [510461] 0 auditory system disease http://www.ebi.ac.uk/efo/EFO_1001455 GCST90079941 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G45.9: Transient cerebral ischemic attack, unspecified (Gene-based burden) 2,495 European ancestry cases, 385,423 European ancestry controls NA Illumina [185344] 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90083815 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72.00: Fracture of unspecified part of neck of femur 1,793 European ancestry cases, 385,858 European ancestry controls NA Affymetrix, Illumina [510456] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081010 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47: Sleep disorders (Gene-based burden) 11,129 European ancestry cases, 364,046 European ancestry controls NA Illumina [185173] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90083821 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K02.9: Dental caries, unspecified 3,669 European ancestry cases, 384,261 European ancestry controls NA Affymetrix, Illumina [510688] 0 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST90080164 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye measures duration (UKB data field 5198) (Gene-based burden) 110,881 European ancestry individuals NA Illumina [168394] 0 sampling time http://www.ebi.ac.uk/efo/EFO_0000689 GCST90083315 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K04.5: Chronic apical periodontitis 601 European ancestry cases, 387,329 European ancestry controls NA Affymetrix, Illumina [510688] 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90080166 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cataract (UKB data field 6148) (Gene-based burden) 18,309 European ancestry cases, 19,489 European ancestry controls NA Illumina [133065] 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90083419 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K04.7: Periapical abscess without sinus 1,228 European ancestry cases, 386,702 European ancestry controls NA Affymetrix, Illumina [510688] 0 periapical tissue disease http://www.ebi.ac.uk/efo/EFO_0010688 GCST90080167 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Diabetes related eye disease (UKB data field 6148) (Gene-based burden) 3,093 European ancestry cases, 34,705 European ancestry controls NA Illumina [133065] 0 diabetic eye disease http://www.ebi.ac.uk/efo/EFO_0009486 GCST90083416 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K08.3: Retained dental root 1,946 European ancestry cases, 385,984 European ancestry controls NA Affymetrix, Illumina [510688] 0 Abnormality of the dentition http://purl.obolibrary.org/obo/HP_0000164 GCST90080172 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glaucoma (UKB data field 6148) (Gene-based burden) 6,848 European ancestry cases, 30,950 European ancestry controls NA Illumina [133065] 0 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90083417 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K08.8: Other specified disorders of teeth and supporting structures 897 European ancestry cases, 387,033 European ancestry controls NA Affymetrix, Illumina [510688] 0 Abnormality of the dentition http://purl.obolibrary.org/obo/HP_0000164 GCST90080173 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Injury loss of vision (UKB data field 6148) (Gene-based burden) 2,794 European ancestry cases, 35,004 European ancestry controls NA Illumina [133065] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90083418 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.1: Ulcer of esophagus 5,969 European ancestry cases, 381,961 European ancestry controls NA Affymetrix, Illumina [510688] 0 esophageal ulcer http://purl.obolibrary.org/obo/MONDO_0044782 GCST90080189 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Macular degeneration (UKB data field 6148) (Gene-based burden) 4,185 European ancestry cases, 33,613 European ancestry controls NA Illumina [133065] 0 macular degeneration http://www.ebi.ac.uk/efo/EFO_0009606 GCST90083420 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K22.8: Other specified diseases of esophagus 1,480 European ancestry cases, 386,448 European ancestry controls NA Affymetrix, Illumina [510688] 0 esophageal disease http://www.ebi.ac.uk/efo/EFO_0009544 GCST90080193 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Other serious eye condition (UKB data field 6148) (Gene-based burden) 8,734 European ancestry cases, 29,064 European ancestry controls NA Illumina [133065] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90083421 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K26.9: Duodenal ulcer, unspecified as acute or chronic, without hemorrhage or perforation 2,705 European ancestry cases, 385,225 European ancestry controls NA Affymetrix, Illumina [510688] 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90080198 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye surgery ever - Yes but more than 4 weeks ago (UKB data field 5181) (Gene-based burden) 8,594 European ancestry cases, 102,287 European ancestry controls NA Illumina [168394] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90083308 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.1: Other acute gastritis 943 European ancestry cases, 386,987 European ancestry controls NA Affymetrix, Illumina [510688] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90080202 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Eye surgery ever - Possibly but more than 4 weeks ago (UKB data field 5181) (Gene-based burden) 651 European ancestry cases, 110,230 European ancestry controls NA Illumina [168394] 0 ophthalmic procedure http://www.ebi.ac.uk/efo/EFO_0010722 GCST90083309 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.5: Unspecified chronic gastritis 3,998 European ancestry cases, 383,932 European ancestry controls NA Affymetrix, Illumina [510688] 0 chronic gastritis http://www.ebi.ac.uk/efo/EFO_0000337 GCST90080203 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Facial pains for three months (UKB data field 4067) (Gene-based burden) 4,032 European ancestry cases, 4,388 European ancestry controls NA Illumina [69962] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90083130 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.6: Other gastritis 6,987 European ancestry cases, 380,943 European ancestry controls NA Affymetrix, Illumina [510688] 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90080204 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Falls in the last year - More than one fall (UKB data field 2296) (Gene-based burden) 30,374 European ancestry cases, 399,492 European ancestry controls NA Illumina [185921] 0 fall http://www.ebi.ac.uk/efo/EFO_0009631 GCST90082871 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K29.8: Duodenitis 9,283 European ancestry cases, 378,647 European ancestry controls NA Affymetrix, Illumina [510688] 0 duodenitis http://purl.obolibrary.org/obo/MONDO_0004627 GCST90080207 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Falls in the last year - Only one fall (UKB data field 2296) (Gene-based burden) 62,653 European ancestry cases, 367,213 European ancestry controls NA Illumina [185921] 0 fall http://www.ebi.ac.uk/efo/EFO_0009631 GCST90082870 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K35.0: Acute appendicitis with generalized peritonitis 729 European ancestry cases, 387,201 European ancestry controls NA Affymetrix, Illumina [510688] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90080214 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Q61: Cystic kidney disease 578 European ancestry cases, 387,104 European ancestry controls NA Affymetrix, Illumina [510455] 2 Cystic Kidney Disease http://www.ebi.ac.uk/efo/EFO_0008615 GCST90080749 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.0: Insomnia (Gene-based burden) 2,507 European ancestry cases, 379,245 European ancestry controls NA Illumina [185277] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90083818 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S30: Superficial injury of abdomen, lower back, pelvis and external genitals 786 European ancestry cases, 386,864 European ancestry controls NA Affymetrix, Illumina [510455] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080965 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.00: Insomnia, unspecified (Gene-based burden) 1,539 European ancestry cases, 381,987 European ancestry controls NA Illumina [185296] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90083817 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E23: Hypofunction and other disorders of the pituitary gland 566 European ancestry cases, 387,112 European ancestry controls NA Affymetrix, Illumina [510454] 0 pituitary gland disease http://www.ebi.ac.uk/efo/EFO_0009607 GCST90079754 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.3: Sleep apnea (Gene-based burden) 5,862 European ancestry cases, 381,677 European ancestry controls NA Illumina [185341] 0 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90083819 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T88: Other complications of surgical and medical care, not elsewhere classified 976 European ancestry cases, 386,677 European ancestry controls NA Affymetrix, Illumina [510454] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081088 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.9: Sleep disorder, unspecified (Gene-based burden) 1,314 European ancestry cases, 385,409 European ancestry controls NA Illumina [185325] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90083820 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J36: Peritonsillar abscess 507 European ancestry cases, 387,145 European ancestry controls NA Affymetrix, Illumina [510453] 0 peritonsillar abscess http://www.ebi.ac.uk/efo/EFO_0007429 GCST90080119 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G50: Disorders of trigeminal nerve (Gene-based burden) 1,034 European ancestry cases, 385,495 European ancestry controls NA Illumina [185317] 0 trigeminal nerve disease http://www.ebi.ac.uk/efo/EFO_0009569 GCST90083823 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M43.1: Spondylolisthesis 1,786 European ancestry cases, 385,893 European ancestry controls NA Affymetrix, Illumina [510453] 0 spondylolisthesis http://www.ebi.ac.uk/efo/EFO_0007493 GCST90080474 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G50.0: Trigeminal neuralgia (Gene-based burden) 502 European ancestry cases, 387,428 European ancestry controls NA Illumina [185344] 0 trigeminal neuralgia http://www.ebi.ac.uk/efo/EFO_1001219 GCST90083822 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D36: Benign neoplasm of other and unspecified sites 899 European ancestry cases, 386,761 European ancestry controls 648 European ancestry cases, 102,157 European ancestry controls Affymetrix, Illumina [510450] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079695 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G51: Facial nerve disorders (Gene-based burden) 1,369 European ancestry cases, 385,508 European ancestry controls NA Illumina [185340] 0 facial nerve disease http://www.ebi.ac.uk/efo/EFO_1002051 GCST90083825 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E04.1: Nontoxic single thyroid nodule 680 European ancestry cases, 386,990 European ancestry controls NA Affymetrix, Illumina [510450] 0 thyroid nodule http://www.ebi.ac.uk/efo/EFO_1001436 GCST90079723 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G51.0: Bell's palsy (Gene-based burden) 878 European ancestry cases, 387,048 European ancestry controls NA Illumina [185344] 0 Bell's palsy http://www.ebi.ac.uk/efo/EFO_0007167 GCST90083824 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J92.9: Pleural plaque without asbestos 668 European ancestry cases, 387,262 European ancestry controls NA Affymetrix, Illumina [510450] 0 pleural disorder http://purl.obolibrary.org/obo/MONDO_0002037 GCST90080150 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G54: Nerve root and plexus disorders (Gene-based burden) 572 European ancestry cases, 386,268 European ancestry controls NA Illumina [185317] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90083826 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.0: Polyarthritis, unspecified 784 European ancestry cases, 386,900 European ancestry controls NA Affymetrix, Illumina [510450] 0 polyarticular arthritis http://purl.obolibrary.org/obo/MONDO_0024280 GCST90080398 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55: Nerve root and plexus compressions in diseases classified elsewhere (Gene-based burden) 5,243 European ancestry cases, 382,644 European ancestry controls NA Illumina [185342] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90083829 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K01: Embedded and impacted teeth 2,066 European ancestry cases, 385,580 European ancestry controls NA Affymetrix, Illumina [510445] 0 Impacted tooth http://purl.obolibrary.org/obo/HP_0011079 GCST90080163 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55.1: Nerve root and plexus compressions in intervertebral disc disorders (Gene-based burden) 4,336 European ancestry cases, 383,594 European ancestry controls NA Illumina [185344] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90083827 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T43: Poisoning by, adverse effect of and underdosing of psychotropic drugs, not elsewhere classified 1,325 European ancestry cases, 386,321 European ancestry controls NA Affymetrix, Illumina [510445] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081056 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G55.2: Nerve root and plexus compressions in spondylosis (Gene-based burden) 662 European ancestry cases, 387,268 European ancestry controls NA Illumina [185344] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90083828 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I60: Nontraumatic subarachnoid hemorrhage 1,067 European ancestry cases, 386,623 European ancestry controls NA Affymetrix, Illumina [510440] 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90080029 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83.0: Cholangitis 750 European ancestry cases, 387,180 European ancestry controls NA Affymetrix, Illumina [510688] 0 Cholangitis http://purl.obolibrary.org/obo/HP_0030151 GCST90080305 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Often (UKB data field 20489) (Gene-based burden) 35,479 European ancestry cases, 103,717 European ancestry controls NA Illumina [172064] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082515 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K83.8: Other specified diseases of biliary tract 1,262 European ancestry cases, 386,668 European ancestry controls NA Affymetrix, Illumina [510688] 0 biliary tract disease http://www.ebi.ac.uk/efo/EFO_0009534 GCST90080307 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Rarely true (UKB data field 20489) (Gene-based burden) 6,336 European ancestry cases, 132,860 European ancestry controls NA Illumina [172064] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082513 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K86.8: Other specified diseases of pancreas 582 European ancestry cases, 387,348 European ancestry controls NA Affymetrix, Illumina [510688] 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90080312 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Sometimes true (UKB data field 20489) (Gene-based burden) 22,598 European ancestry cases, 116,598 European ancestry controls NA Illumina [172064] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082514 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K91.4: Colostomy and enterostomy malfunction 635 European ancestry cases, 387,295 European ancestry controls NA Affymetrix, Illumina [510688] 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90080316 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Very often true (UKB data field 20489) (Gene-based burden) 72,864 European ancestry cases, 66,332 European ancestry controls NA Illumina [172064] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082516 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.0: Cellulitis and acute lymphangitis of finger and toe 692 European ancestry cases, 387,237 European ancestry controls NA Affymetrix, Illumina [510688] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90080327 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - A little bit (UKB data field 20498) (Gene-based burden) 39,340 European ancestry cases, 100,162 European ancestry controls NA Illumina [172106] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082536 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L60.0: Ingrowing nail 928 European ancestry cases, 387,002 European ancestry controls NA Affymetrix, Illumina [510688] 0 nail anomaly http://purl.obolibrary.org/obo/MONDO_0019283 GCST90080356 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - Extremely (UKB data field 20498) (Gene-based burden) 1,284 European ancestry cases, 138,218 European ancestry controls NA Illumina [172106] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082539 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L72.1: Pilar and trichodermal cyst 5,572 European ancestry cases, 382,358 European ancestry controls 201 European ancestry cases, 93,588 European ancestry controls Affymetrix, Illumina [510688] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080362 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - Moderately (UKB data field 20498) (Gene-based burden) 7,409 European ancestry cases, 132,093 European ancestry controls NA Illumina [172106] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082537 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L89.1: Pressure ulcer of back 604 European ancestry cases, 387,326 European ancestry controls NA Affymetrix, Illumina [510688] 0 chronic ulcer of skin http://www.ebi.ac.uk/efo/EFO_0007066 GCST90080373 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt very upset when reminded of stressful experience in past month - Quite a bit (UKB data field 20498) (Gene-based burden) 4,459 European ancestry cases, 135,043 European ancestry controls NA Illumina [172106] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082538 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L90.0: Lichen sclerosus et atrophicus 555 European ancestry cases, 387,375 European ancestry controls NA Affymetrix, Illumina [510688] 0 lichen sclerosus et atrophicus http://purl.obolibrary.org/obo/MONDO_0007899 GCST90080375 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. FEV1 FVC ratio Z score (UKB data field 20258) (Gene-based burden) 343,302 European ancestry individuals NA Illumina [184375] 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90082376 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.90: Rheumatoid arthritis, unspecified 1,306 European ancestry cases, 386,624 European ancestry controls NA Affymetrix, Illumina [510688] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90080389 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fever when IBS symptoms first began (UKB data field 21073) (Gene-based burden) 1,303 European ancestry cases, 17,177 European ancestry controls NA Illumina [103107] 0 Fever http://purl.obolibrary.org/obo/HP_0001945 GCST90082822 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06.99: Rheumatoid arthritis, unspecified 2,622 European ancestry cases, 385,308 European ancestry controls NA Affymetrix, Illumina [510688] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90080390 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 14 (20165) (Gene-based burden) 797 European ancestry cases, 108,689 European ancestry controls NA Illumina [166792] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082313 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.9: Arthritis, unspecified 15,502 European ancestry cases, 372,428 European ancestry controls NA Affymetrix, Illumina [510688] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90080404 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 15 (20165) (Gene-based burden) 106,700 European ancestry cases, 2,786 European ancestry controls NA Illumina [166792] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082314 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.90: Arthritis, unspecified 1,283 European ancestry cases, 386,647 European ancestry controls NA Affymetrix, Illumina [510688] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90080399 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S01.0: Open wound of scalp 1,032 European ancestry cases, 386,667 European ancestry controls NA Affymetrix, Illumina [510481] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080942 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F53: Puerperal psychosis (Gene-based burden) 2,567 European ancestry cases, 204,976 European ancestry controls NA Illumina [179678] 0 psychosis http://www.ebi.ac.uk/efo/EFO_0005407 GCST90083802 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G30: Alzheimer's disease 890 European ancestry cases, 386,784 European ancestry controls NA Affymetrix, Illumina [510480] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90079819 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G20: Parkinson's disease (Gene-based burden) 1,827 European ancestry cases, 385,837 European ancestry controls NA Illumina [185339] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90083803 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K09: Cysts of oral region, not elsewhere classified 514 European ancestry cases, 387,207 European ancestry controls NA Affymetrix, Illumina [510480] 0 Mediastinal Cyst http://www.ebi.ac.uk/efo/EFO_1001368 GCST90080175 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G25: Other extrapyramidal and movement disorders (Gene-based burden) 1,721 European ancestry cases, 384,069 European ancestry controls NA Illumina [185308] 0 movement disorder http://www.ebi.ac.uk/efo/EFO_0004280 GCST90083804 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S72.0: Fracture of head and neck of femur 1,990 European ancestry cases, 385,682 European ancestry controls NA Affymetrix, Illumina [510480] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081011 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G30: Alzheimer's disease (Gene-based burden) 890 European ancestry cases, 386,784 European ancestry controls NA Illumina [185340] 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90083805 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R91: Abnormal findings on diagnostic imaging of lung 3,443 European ancestry cases, 384,244 European ancestry controls NA Affymetrix, Illumina [510479] 0 Abnormal lung morphology http://purl.obolibrary.org/obo/HP_0002088 GCST90080927 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G31: Other degenerative diseases of nervous system, not elsewhere classified (Gene-based burden) 1,010 European ancestry cases, 386,604 European ancestry controls NA Illumina [185344] 0 neurodegenerative disease http://www.ebi.ac.uk/efo/EFO_0005772 GCST90083807 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H02.8: Other specified disorders of eyelid 2,358 European ancestry cases, 385,294 European ancestry controls NA Affymetrix, Illumina [510477] 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90079872 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G31.9: Degenerative disease of nervous system, unspecified (Gene-based burden) 569 European ancestry cases, 387,296 European ancestry controls NA Illumina [185344] 0 neurodegenerative disease http://www.ebi.ac.uk/efo/EFO_0005772 GCST90083806 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51.1: Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy 4,203 European ancestry cases, 383,475 European ancestry controls NA Affymetrix, Illumina [510475] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90080495 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G35: Multiple sclerosis (Gene-based burden) 1,634 European ancestry cases, 386,134 European ancestry controls NA Illumina [185342] 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90083808 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 D12: Benign neoplasm of colon, rectum, anus and anal canal 16,948 European ancestry cases, 370,732 European ancestry controls 10,988 European ancestry cases, 84,953 European ancestry controls Affymetrix, Illumina [510472] 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90079662 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40: Epilepsy and recurrent seizures (Gene-based burden) 4,885 European ancestry cases, 382,224 European ancestry controls NA Illumina [185330] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90083811 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T83: Complications of genitourinary prosthetic devices, implants and grafts 1,621 European ancestry cases, 386,046 European ancestry controls NA Affymetrix, Illumina [510472] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081077 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G40.3: Generalized idiopathic epilepsy and epileptic syndromes (Gene-based burden) 510 European ancestry cases, 387,420 European ancestry controls NA Illumina [185344] 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90083809 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever thought that life not worth living once (UKB data field 20479) (Gene-based burden) 19,030 European ancestry cases, 119,752 European ancestry controls NA Illumina [171997] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082496 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J92.0: Pleural plaque with presence of asbestos 573 European ancestry cases, 387,357 European ancestry controls NA Affymetrix, Illumina [510688] 0 pleural disorder http://purl.obolibrary.org/obo/MONDO_0002037 GCST90080149 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever unenthusiastic/disinterested for a whole week (UKB data field 4631) (Gene-based burden) 63,612 European ancestry cases, 107,337 European ancestry controls NA Illumina [176452] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90083199 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J93.9: Pneumothorax, unspecified 837 European ancestry cases, 387,093 European ancestry controls NA Affymetrix, Illumina [510688] 0 pneumothorax http://purl.obolibrary.org/obo/MONDO_0002076 GCST90080152 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever used hormone replacement therapy (UKB data field 2814) (Gene-based burden) 92,655 European ancestry cases, 140,348 European ancestry controls NA Illumina [181122] 0 hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0003961 GCST90082948 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K01.1: Impacted teeth 1,967 European ancestry cases, 385,963 European ancestry controls NA Affymetrix, Illumina [510688] 0 Impacted tooth http://purl.obolibrary.org/obo/HP_0011079 GCST90080162 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Ever worried more than most people would in similar situation (UKB data field 20425) (Gene-based burden) 30,487 European ancestry cases, 86,633 European ancestry controls NA Illumina [168225] 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90082428 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G31: Other degenerative diseases of nervous system, not elsewhere classified 1,010 European ancestry cases, 386,604 European ancestry controls NA Affymetrix, Illumina [510415] 0 neurodegenerative disease http://www.ebi.ac.uk/efo/EFO_0005772 GCST90079821 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G93: Other disorders of brain (Gene-based burden) 2,591 European ancestry cases, 383,973 European ancestry controls NA Illumina [185325] 0 brain disease http://www.ebi.ac.uk/efo/EFO_0005774 GCST90083844 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K82: Other diseases of gallbladder 2,278 European ancestry cases, 385,325 European ancestry controls NA Affymetrix, Illumina [510415] 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90080304 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G93.3: Postviral fatigue syndrome (Gene-based burden) 817 European ancestry cases, 386,637 European ancestry controls NA Illumina [185336] 0 chronic fatigue syndrome http://www.ebi.ac.uk/efo/EFO_0004540 GCST90083843 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22.0: Fracture of thoracic vertebra 568 European ancestry cases, 387,032 European ancestry controls NA Affymetrix, Illumina [510415] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080959 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G95: Other and unspecified diseases of spinal cord (Gene-based burden) 815 European ancestry cases, 386,806 European ancestry controls NA Illumina [185331] 0 spinal cord disease http://www.ebi.ac.uk/efo/EFO_0009488 GCST90083845 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K75: Other inflammatory liver diseases 965 European ancestry cases, 386,663 European ancestry controls NA Affymetrix, Illumina [510414] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90080287 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K64.9: Unspecified hemorrhoids 1,717 European ancestry cases, 386,213 European ancestry controls NA Affymetrix, Illumina [510688] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90080276 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Never true (UKB data field 20487) (Gene-based burden) 118,008 European ancestry cases, 21,317 European ancestry controls NA Illumina [172091] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082507 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.0: Fatty (change of) liver, not elsewhere classified 2,432 European ancestry cases, 385,498 European ancestry controls NA Affymetrix, Illumina [510688] 0 fatty liver disease http://purl.obolibrary.org/obo/MONDO_0004790 GCST90080288 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Often (UKB data field 20487) (Gene-based burden) 2,135 European ancestry cases, 137,190 European ancestry controls NA Illumina [172091] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082510 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.6: Portal hypertension 753 European ancestry cases, 387,177 European ancestry controls 671 European ancestry cases, 106,200 European ancestry controls Affymetrix, Illumina [510688] 0 portal hypertension http://www.ebi.ac.uk/efo/EFO_0000666 GCST90080289 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Rarely true (UKB data field 20487) (Gene-based burden) 8,351 European ancestry cases, 130,974 European ancestry controls NA Illumina [172091] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082508 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K76.8: Other specified diseases of liver 1,267 European ancestry cases, 386,661 European ancestry controls NA Affymetrix, Illumina [510688] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90080290 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Sometimes true (UKB data field 20487) (Gene-based burden) 9,087 European ancestry cases, 130,238 European ancestry controls NA Illumina [172091] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082509 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.0: Calculus of gallbladder with acute cholecystitis 1,911 European ancestry cases, 386,019 European ancestry controls NA Affymetrix, Illumina [510688] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90080293 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt hated by family member as a child - Very often true (UKB data field 20487) (Gene-based burden) 1,744 European ancestry cases, 137,581 European ancestry controls NA Illumina [172091] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082511 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.1: Calculus of gallbladder with other cholecystitis 6,359 European ancestry cases, 381,571 European ancestry controls NA Affymetrix, Illumina [510688] 0 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90080294 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt irritable or had angry outbursts in past month - A little bit (UKB data field 20494) (Gene-based burden) 20,254 European ancestry cases, 42,559 European ancestry controls NA Illumina [151326] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082521 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K80.5: Calculus of bile duct without cholangitis or cholecystitis 2,940 European ancestry cases, 384,990 European ancestry controls NA Affymetrix, Illumina [510688] 0 acalculous cholecystitis http://www.ebi.ac.uk/efo/EFO_1000790 GCST90080296 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt irritable or had angry outbursts in past month - Moderately (UKB data field 20494) (Gene-based burden) 3,089 European ancestry cases, 59,724 European ancestry controls NA Illumina [151326] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082522 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81.1: Chronic cholecystitis 1,530 European ancestry cases, 386,400 European ancestry controls NA Affymetrix, Illumina [510688] 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90080299 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt irritable or had angry outbursts in past month - Quite a bit (UKB data field 20494) (Gene-based burden) 1,761 European ancestry cases, 61,052 European ancestry controls NA Illumina [151326] 0 emotional symptom measurement http://www.ebi.ac.uk/efo/EFO_0007803 GCST90082523 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K82.4: Cholesterolosis of gallbladder 558 European ancestry cases, 387,372 European ancestry controls NA Affymetrix, Illumina [510688] 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90080302 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Felt loved as a child - Never true (UKB data field 20489) (Gene-based burden) 1,919 European ancestry cases, 137,277 European ancestry controls NA Illumina [172064] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082512 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family history of IBS (UKB data field 21065) (Gene-based burden) 21,959 European ancestry cases, 110,628 European ancestry controls NA Illumina [170642] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90082815 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K35.9: Acute appendicitis, unspecified 1,587 European ancestry cases, 386,343 European ancestry controls NA Affymetrix, Illumina [510688] 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90080215 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Extremely happy (UKB data field 4559) (Gene-based burden) 37,735 European ancestry cases, 138,353 European ancestry controls NA Illumina [177025] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90083180 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K41.9: Unilateral femoral hernia, without obstruction or gangrene 629 European ancestry cases, 387,301 European ancestry controls NA Affymetrix, Illumina [510688] 0 femoral hernia http://www.ebi.ac.uk/efo/EFO_1001791 GCST90080221 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Extremely unhappy (UKB data field 4559) (Gene-based burden) 985 European ancestry cases, 175,103 European ancestry controls NA Illumina [177025] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90083185 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K43.9: Ventral hernia without obstruction or gangrene 3,779 European ancestry cases, 384,151 European ancestry controls NA Affymetrix, Illumina [510688] 0 ventral hernia http://www.ebi.ac.uk/efo/EFO_1001866 GCST90080225 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Moderately happy (UKB data field 4559) (Gene-based burden) 51,919 European ancestry cases, 124,169 European ancestry controls NA Illumina [177025] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90083182 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K50.1: Crohn's disease of large intestine 591 European ancestry cases, 387,339 European ancestry controls NA Affymetrix, Illumina [510688] 0 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90080230 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Moderately unhappy (UKB data field 4559) (Gene-based burden) 8,490 European ancestry cases, 167,598 European ancestry controls NA Illumina [177025] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90083183 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K51.9: Ulcerative colitis, unspecified 3,242 European ancestry cases, 384,687 European ancestry controls NA Affymetrix, Illumina [510688] 0 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90080233 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Very happy (UKB data field 4559) (Gene-based burden) 84,228 European ancestry cases, 91,860 European ancestry controls NA Illumina [177025] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90083181 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52.8: Other specified noninfective gastroenteritis and colitis 650 European ancestry cases, 387,279 European ancestry controls NA Affymetrix, Illumina [510688] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90080235 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Family relationship satisfaction - Very unhappy (UKB data field 4559) (Gene-based burden) 2,347 European ancestry cases, 173,741 European ancestry controls NA Illumina [177025] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90083184 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K56.5: Intestinal adhesions [bands] with obstruction (postinfection) 1,110 European ancestry cases, 386,820 European ancestry controls NA Affymetrix, Illumina [510688] 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90080241 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Father still alive (UKB data field 1797) (Gene-based burden) 96,906 European ancestry cases, 322,692 European ancestry controls NA Illumina [185792] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90081599 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58.0: Irritable bowel syndrome with diarrhea 543 European ancestry cases, 387,387 European ancestry controls NA Affymetrix, Illumina [510688] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90080250 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Paternal age (UKB data field 2946) (Gene-based burden) 96,287 European ancestry individuals NA Illumina [164175] 0 parental longevity http://www.ebi.ac.uk/efo/EFO_0007796 GCST90082960 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58.9: Irritable bowel syndrome without diarrhea 6,678 European ancestry cases, 381,252 European ancestry controls NA Affymetrix, Illumina [510688] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90080251 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Paternal age at death (UKB data field 1807) (Gene-based burden) 324,038 European ancestry individuals NA Illumina [183984] 0 father's age at death http://www.ebi.ac.uk/efo/EFO_0009712 GCST90081600 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60.1: Chronic anal fissure 577 European ancestry cases, 387,353 European ancestry controls NA Affymetrix, Illumina [510688] 0 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90080256 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Fed up feelings (UKB data field 1960) (Gene-based burden) 176,598 European ancestry cases, 245,905 European ancestry controls NA Illumina [185813] 0 feeling "fed-up" measurement http://www.ebi.ac.uk/efo/EFO_0009588 GCST90081608 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60.2: Anal fissure, unspecified 1,863 European ancestry cases, 386,067 European ancestry controls NA Affymetrix, Illumina [510688] 0 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90080257 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Feelings of tiredness during worst episode of depression (UKB data field 20449) (Gene-based burden) 58,240 European ancestry cases, 12,695 European ancestry controls NA Illumina [154848] 0 Fatigue http://purl.obolibrary.org/obo/HP_0012378 GCST90082456 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K60.3: Anal fistula 1,370 European ancestry cases, 386,560 European ancestry controls NA Affymetrix, Illumina [510688] 0 Anal fistula http://purl.obolibrary.org/obo/HP_0010447 GCST90080258 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Feelings of worthlessness during worst period of depression (UKB data field 20450) (Gene-based burden) 37,621 European ancestry cases, 36,176 European ancestry controls NA Illumina [156049] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90082457 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56: Mononeuropathies of upper limb (Gene-based burden) 13,929 European ancestry cases, 368,599 European ancestry controls NA Illumina [185264] 0 mononeuropathy http://www.ebi.ac.uk/efo/EFO_0009558 GCST90083832 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.6: Allergy status to analgesic agent status 5,809 European ancestry cases, 381,836 European ancestry controls NA Affymetrix, Illumina [510439] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081385 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56.0: Carpal tunnel syndrome (Gene-based burden) 11,271 European ancestry cases, 376,659 European ancestry controls NA Illumina [185344] 0 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90083830 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J90: Pleural effusion, not elsewhere classified 7,231 European ancestry cases, 380,404 European ancestry controls NA Affymetrix, Illumina [510437] 0 pleural effusion http://www.ebi.ac.uk/efo/EFO_0009637 GCST90080148 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56.2: Lesion of ulnar nerve (Gene-based burden) 1,388 European ancestry cases, 386,542 European ancestry controls NA Illumina [185344] 0 ulnar nerve lesion http://purl.obolibrary.org/obo/MONDO_0001458 GCST90083831 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K81.9: Cholecystitis, unspecified 940 European ancestry cases, 386,668 European ancestry controls NA Affymetrix, Illumina [510437] 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90080300 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G57: Mononeuropathies of lower limb (Gene-based burden) 2,301 European ancestry cases, 383,611 European ancestry controls NA Illumina [185312] 0 mononeuropathy http://www.ebi.ac.uk/efo/EFO_0009558 GCST90083834 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z02.8: Encounter for other administrative examinations 3,011 European ancestry cases, 384,651 European ancestry controls NA Affymetrix, Illumina [510434] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081185 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G57.6: Lesion of plantar nerve (Gene-based burden) 1,560 European ancestry cases, 386,370 European ancestry controls NA Illumina [185344] 0 peripheral nerve lesion http://purl.obolibrary.org/obo/MONDO_0024334 GCST90083833 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R16: Hepatomegaly and splenomegaly, not elsewhere classified 864 European ancestry cases, 386,770 European ancestry controls 1,795 European ancestry cases, 75,109 European ancestry controls Affymetrix, Illumina [510433] 1 Hepatomegaly, Splenomegaly http://purl.obolibrary.org/obo/HP_0002240, http://purl.obolibrary.org/obo/HP_0001744 GCST90080805 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G62: Other and unspecified polyneuropathies (Gene-based burden) 1,972 European ancestry cases, 384,992 European ancestry controls NA Illumina [185335] 0 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90083836 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E16.2: Hypoglycemia, unspecified 1,319 European ancestry cases, 386,316 European ancestry controls NA Affymetrix, Illumina [510431] 0 Hypoglycemia http://purl.obolibrary.org/obo/HP_0001943 GCST90079749 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G62.9: Polyneuropathy, unspecified (Gene-based burden) 1,543 European ancestry cases, 385,937 European ancestry controls NA Illumina [185340] 0 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90083835 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T79: Certain early complications of trauma, not elsewhere classified 625 European ancestry cases, 387,014 European ancestry controls NA Affymetrix, Illumina [510431] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081067 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G63: Polyneuropathy in diseases classified elsewhere (Gene-based burden) 586 European ancestry cases, 387,338 European ancestry controls NA Illumina [185343] 0 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90083838 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G95: Other and unspecified diseases of spinal cord 815 European ancestry cases, 386,806 European ancestry controls NA Affymetrix, Illumina [510429] 0 spinal cord disease http://www.ebi.ac.uk/efo/EFO_0009488 GCST90079859 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G63.2: Diabetic polyneuropathy (Gene-based burden) 538 European ancestry cases, 387,392 European ancestry controls NA Illumina [185344] 0 diabetic polyneuropathy http://purl.obolibrary.org/obo/MONDO_0001583 GCST90083837 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J92: Pleural plaque 1,162 European ancestry cases, 386,480 European ancestry controls NA Affymetrix, Illumina [510428] 0 pleural disorder http://purl.obolibrary.org/obo/MONDO_0002037 GCST90080151 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G81: Hemiplegia and hemiparesis (Gene-based burden) 2,070 European ancestry cases, 385,551 European ancestry controls NA Illumina [185341] 0 hemiplegia, Hemiparesis http://www.ebi.ac.uk/efo/EFO_0009453, http://purl.obolibrary.org/obo/HP_0001269 GCST90083840 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G20: Parkinson's disease 1,827 European ancestry cases, 385,837 European ancestry controls NA Affymetrix, Illumina [510427] 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90079817 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G81.9: Hemiplegia, unspecified (Gene-based burden) 2,024 European ancestry cases, 385,757 European ancestry controls NA Illumina [185342] 0 hemiplegia http://www.ebi.ac.uk/efo/EFO_0009453 GCST90083839 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S51: Open wound of elbow and forearm 609 European ancestry cases, 387,015 European ancestry controls NA Affymetrix, Illumina [510424] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080983 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G83: Other paralytic syndromes (Gene-based burden) 539 European ancestry cases, 386,953 European ancestry controls NA Illumina [185324] 0 paralytic strabismus http://www.ebi.ac.uk/efo/EFO_0009678 GCST90083841 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z41.1: Encounter for cosmetic surgery 852 European ancestry cases, 386,781 European ancestry controls NA Affymetrix, Illumina [510419] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081255 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G91: Hydrocephalus (Gene-based burden) 595 European ancestry cases, 387,290 European ancestry controls NA Illumina [185344] 0 Hydrocephalus http://purl.obolibrary.org/obo/HP_0000238 GCST90083842 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 16 (20165) (Gene-based burden) 1,166 European ancestry cases, 108,320 European ancestry controls NA Illumina [166792] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082315 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.94: Arthritis, unspecified 1,004 European ancestry cases, 386,926 European ancestry controls NA Affymetrix, Illumina [510688] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90080400 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 13 (4935) (Gene-based burden) 734 European ancestry cases, 169,393 European ancestry controls NA Illumina [176325] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083215 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.96: Arthritis, unspecified 1,141 European ancestry cases, 386,789 European ancestry controls NA Affymetrix, Illumina [510688] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90080401 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 14 (4935) (Gene-based burden) 1,767 European ancestry cases, 168,407 European ancestry controls NA Illumina [176330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083216 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.97: Arthritis, unspecified 774 European ancestry cases, 387,156 European ancestry controls NA Affymetrix, Illumina [510688] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90080402 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 15 (4935) (Gene-based burden) 165,470 European ancestry cases, 4,704 European ancestry controls NA Illumina [176330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083217 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M13.99: Arthritis, unspecified 4,690 European ancestry cases, 383,240 European ancestry controls NA Affymetrix, Illumina [510688] 0 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90080403 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 16 (4935) (Gene-based burden) 2,280 European ancestry cases, 167,894 European ancestry controls NA Illumina [176330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083218 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M15.0: Primary generalized (osteo)arthritis 550 European ancestry cases, 387,380 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080406 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI1 numeric addition test - 17 (4935) (Gene-based burden) 881 European ancestry cases, 169,293 European ancestry controls NA Illumina [176330] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90083219 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16.0: Bilateral primary osteoarthritis of hip 884 European ancestry cases, 387,046 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90080409 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 92 (UKB data field 20183) (Gene-based burden) 571 European ancestry cases, 18,959 European ancestry controls NA Illumina [104855] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082351 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16.1: Unilateral primary osteoarthritis of hip 3,961 European ancestry cases, 383,969 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90080410 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 93 (UKB data field 20183) (Gene-based burden) 1,095 European ancestry cases, 18,435 European ancestry controls NA Illumina [104855] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082350 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M16.9: Osteoarthritis of hip, unspecified 11,093 European ancestry cases, 376,837 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90080411 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 94 (UKB data field 20183) (Gene-based burden) 917 European ancestry cases, 18,613 European ancestry controls NA Illumina [104855] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082349 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17.0: Bilateral primary osteoarthritis of knee 1,430 European ancestry cases, 386,500 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90080413 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 95 (UKB data field 20183) (Gene-based burden) 16,244 European ancestry cases, 3,286 European ancestry controls NA Illumina [104855] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082348 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M18.9: Osteoarthritis of first carpometacarpal joint, unspecified 1,352 European ancestry cases, 386,578 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080417 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Cognitive function - FI10 arithmetic sequence recognition - 96 (UKB data field 20183) (Gene-based burden) 703 European ancestry cases, 18,827 European ancestry controls NA Illumina [104855] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90082347 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.91: Primary osteoarthritis, unspecified site 2,523 European ancestry cases, 385,407 European ancestry controls NA Affymetrix, Illumina [510688] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080422 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G99: Other disorders of nervous system in diseases classified elsewhere (Gene-based burden) 1,401 European ancestry cases, 386,517 European ancestry controls NA Illumina [185344] 0 nervous system disease http://www.ebi.ac.uk/efo/EFO_0000618 GCST90083847 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R41.0: Disorientation, unspecified 3,254 European ancestry cases, 384,332 European ancestry controls NA Affymetrix, Illumina [510410] 0 Cognitive impairment http://purl.obolibrary.org/obo/HP_0100543 GCST90080854 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G99.2: Myelopathy in diseases classified elsewhere (Gene-based burden) 1,259 European ancestry cases, 386,671 European ancestry controls NA Illumina [185344] 0 Myelopathy http://purl.obolibrary.org/obo/HP_0002196 GCST90083846 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M71.2: Synovial cyst of popliteal space [Baker] (Gene-based burden) 560 European ancestry cases, 387,370 European ancestry controls NA Illumina [185344] 0 synovium disorder http://purl.obolibrary.org/obo/MONDO_0056799 GCST90084513 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M67: Other disorders of synovium and tendon 5,503 European ancestry cases, 375,456 European ancestry controls NA Affymetrix, Illumina [504587] 0 tenosynovitis http://www.ebi.ac.uk/efo/EFO_1001435 GCST90080524 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M72: Fibroblastic disorders (Gene-based burden) 8,539 European ancestry cases, 367,694 European ancestry controls NA Illumina [185179] 0 fibroblastic disorder http://www.ebi.ac.uk/efo/EFO_0009432 GCST90084517 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83: Varicose veins of lower extremities 15,125 European ancestry cases, 365,783 European ancestry controls 3,968 European ancestry cases, 107,805 European ancestry controls Affymetrix, Illumina [504565] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90080066 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M72.0: Palmar fascial fibromatosis [Dupuytren] (Gene-based burden) 4,263 European ancestry cases, 383,667 European ancestry controls NA Illumina [185344] 0 Palmar Fibromatosis http://www.ebi.ac.uk/efo/EFO_1000438 GCST90084516 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z87.09: Personal history of other diseases of the respiratory system 2,125 European ancestry cases, 378,842 European ancestry controls NA Affymetrix, Illumina [504548] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90081366 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M72.04: Palmar fascial fibromatosis [Dupuytren] (Gene-based burden) 1,695 European ancestry cases, 386,235 European ancestry controls NA Illumina [185344] 0 Palmar Fibromatosis http://www.ebi.ac.uk/efo/EFO_1000438 GCST90084515 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W19: Unspecified fall 8,510 European ancestry cases, 372,626 European ancestry controls NA Affymetrix, Illumina [504524] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081120 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75: Shoulder lesions (Gene-based burden) 16,150 European ancestry cases, 358,370 European ancestry controls NA Illumina [185147] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084523 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H69: Other and unspecified disorders of Eustachian tube 1,569 European ancestry cases, 379,457 European ancestry controls NA Affymetrix, Illumina [504523] 0 eustachian tube disease http://www.ebi.ac.uk/efo/EFO_0009667 GCST90079936 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.0: Adhesive capsulitis of shoulder (Gene-based burden) 1,966 European ancestry cases, 385,964 European ancestry controls NA Illumina [185344] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084518 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.29: Personal history of other drug therapy 1,706 European ancestry cases, 379,051 European ancestry controls NA Affymetrix, Illumina [504437] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081405 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.1: Rotator cuff tear or rupture, not specified as traumatic (Gene-based burden) 4,628 European ancestry cases, 382,991 European ancestry controls NA Illumina [185339] 0 rotator cuff tear http://www.ebi.ac.uk/efo/EFO_1001250 GCST90084519 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z28.3: Underimmunization status 2,689 European ancestry cases, 378,103 European ancestry controls NA Affymetrix, Illumina [504383] 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90081227 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.4: Impingement syndrome of shoulder (Gene-based burden) 6,024 European ancestry cases, 381,906 European ancestry controls NA Illumina [185344] 0 shoulder impingement syndrome http://www.ebi.ac.uk/efo/EFO_1001178 GCST90084520 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.2: Personal history of drug therapy 23,381 European ancestry cases, 357,348 European ancestry controls 422 European ancestry cases, 34,686 European ancestry controls Affymetrix, Illumina [504374] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081406 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M75.5: Bursitis of shoulder (Gene-based burden) 895 European ancestry cases, 387,035 European ancestry controls NA Illumina [185344] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084521 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.8: Unspecified haemorrhoids with other complications (Gene-based burden) 3,859 European ancestry cases, 384,071 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084058 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 P29.1: Neonatal cardiac dysrhythmia 1,784 European ancestry cases, 384,880 European ancestry controls NA Affymetrix, Illumina [509668] 0 perinatal disease http://www.ebi.ac.uk/efo/EFO_0010238 GCST90080745 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.9: Unspecified haemorrhoids without complication (Gene-based burden) 14,954 European ancestry cases, 372,976 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084059 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 P29.12: Neonatal bradycardia 1,784 European ancestry cases, 384,880 European ancestry controls NA Affymetrix, Illumina [509668] 0 perinatal disease http://www.ebi.ac.uk/efo/EFO_0010238 GCST90080744 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I85: Esophageal varices (Gene-based burden) 684 European ancestry cases, 387,221 European ancestry controls NA Illumina [185344] 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90084062 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R74: Abnormal serum enzyme levels 652 European ancestry cases, 386,128 European ancestry controls NA Affymetrix, Illumina [509663] 0 abnormality of serum enzyme levels http://www.ebi.ac.uk/efo/EFO_0009826 GCST90080908 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I85.9: Oesophageal varices without bleeding (Gene-based burden) 643 European ancestry cases, 387,287 European ancestry controls NA Illumina [185329] 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90084061 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.4: Lumbago with sciatica 1,022 European ancestry cases, 385,719 European ancestry controls NA Affymetrix, Illumina [509659] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90080506 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M53: Other and unspecified dorsopathies, not elsewhere classified (Gene-based burden) 1,469 European ancestry cases, 382,067 European ancestry controls NA Illumina [185244] 0 vertebral disorder http://purl.obolibrary.org/obo/MONDO_0045002 GCST90084485 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M20: Acquired deformities of fingers and toes 12,930 European ancestry cases, 368,891 European ancestry controls NA Affymetrix, Illumina [505221] 0 congenital deformities of fingers http://purl.obolibrary.org/obo/MONDO_0017428 GCST90080432 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54: Dorsalgia (Gene-based burden) 50,434 European ancestry cases, 288,924 European ancestry controls NA Illumina [184499] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90084499 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63: Symptoms and signs concerning food and fluid intake 9,824 European ancestry cases, 372,091 European ancestry controls NA Affymetrix, Illumina [505211] 0 sign or symptom concerning food and fluid intake http://www.ebi.ac.uk/efo/EFO_0009825 GCST90080896 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.1: Radiculopathy (Gene-based burden) 1,154 European ancestry cases, 386,776 European ancestry controls NA Illumina [185344] 0 radiculopathy http://purl.obolibrary.org/obo/MONDO_0002959 GCST90084486 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R60.9: Edema, unspecified 2,772 European ancestry cases, 378,986 European ancestry controls NA Affymetrix, Illumina [505168] 0 edema http://www.ebi.ac.uk/efo/EFO_0009373 GCST90080889 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.2: Cervicalgia (Gene-based burden) 6,608 European ancestry cases, 370,716 European ancestry controls NA Illumina [185163] 0 Neck pain http://purl.obolibrary.org/obo/HP_0030833 GCST90084488 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J34: Other and unspecified disorders of nose and nasal sinuses 8,558 European ancestry cases, 373,094 European ancestry controls NA Affymetrix, Illumina [505166] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080117 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.22: Cervicalgia (Gene-based burden) 1,083 European ancestry cases, 386,847 European ancestry controls NA Illumina [185344] 0 Neck pain http://purl.obolibrary.org/obo/HP_0030833 GCST90084487 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S83: Dislocation and sprain of joints and ligaments of knee 1,620 European ancestry cases, 379,952 European ancestry controls NA Affymetrix, Illumina [505155] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90081031 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.3: Sciatica (Gene-based burden) 5,711 European ancestry cases, 373,607 European ancestry controls NA Illumina [185227] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90084491 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z76.0: Encounter for issue of repeat prescription 4,934 European ancestry cases, 376,664 European ancestry controls NA Affymetrix, Illumina [505116] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081322 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.30: Sciatica, unspecified side (Gene-based burden) 3,519 European ancestry cases, 375,578 European ancestry controls NA Illumina [185218] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90084489 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M85: Other disorders of bone density and structure 4,030 European ancestry cases, 377,290 European ancestry controls NA Affymetrix, Illumina [505097] 0 Abnormality of bone mineral density http://purl.obolibrary.org/obo/HP_0004348 GCST90080563 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.39: Sciatica (Gene-based burden) 681 European ancestry cases, 387,249 European ancestry controls NA Illumina [185344] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90084490 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K52: Other and unspecified noninfective gastroenteritis and colitis 19,104 European ancestry cases, 362,399 European ancestry controls NA Affymetrix, Illumina [505086] 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90080237 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.4: Lumbago with sciatica (Gene-based burden) 1,022 European ancestry cases, 385,719 European ancestry controls NA Illumina [185303] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90084492 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R29: Other symptoms and signs involving the nervous and musculoskeletal systems 6,035 European ancestry cases, 375,445 European ancestry controls NA Affymetrix, Illumina [505078] 0 Abnormality of the nervous system, Abnormality of the musculature, Abnormality of the skeletal system http://purl.obolibrary.org/obo/HP_0000707, http://purl.obolibrary.org/obo/HP_0003011, http://purl.obolibrary.org/obo/HP_0000924 GCST90080836 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.5: Low back pain (Gene-based burden) 22,734 European ancestry cases, 341,460 European ancestry controls NA Illumina [184955] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90084496 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L21: Seborrheic dermatitis 2,156 European ancestry cases, 379,083 European ancestry controls NA Affymetrix, Illumina [505041] 0 seborrheic dermatitis http://www.ebi.ac.uk/efo/EFO_1000764 GCST90080338 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.56: Low back pain (Gene-based burden) 2,859 European ancestry cases, 385,071 European ancestry controls NA Illumina [185344] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90084493 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z84.89: Family history of other specified conditions 920 European ancestry cases, 380,626 European ancestry controls NA Affymetrix, Illumina [505033] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081344 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.57: Low back pain (Gene-based burden) 1,038 European ancestry cases, 386,892 European ancestry controls NA Illumina [185344] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90084494 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z84.8: Family history of other specified conditions 1,025 European ancestry cases, 380,498 European ancestry controls NA Affymetrix, Illumina [505009] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081345 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.59: Low back pain (Gene-based burden) 2,457 European ancestry cases, 385,473 European ancestry controls NA Illumina [185344] 0 Low back pain http://purl.obolibrary.org/obo/HP_0003419 GCST90084495 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.0: Insomnia 2,507 European ancestry cases, 379,245 European ancestry controls NA Affymetrix, Illumina [505008] 0 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90079832 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.9: Dorsalgia, unspecified (Gene-based burden) 13,158 European ancestry cases, 358,552 European ancestry controls NA Illumina [185072] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90084498 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21.9: Gastro-esophageal reflux disease without esophagitis 22,340 European ancestry cases, 359,319 European ancestry controls NA Affymetrix, Illumina [504997] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90080187 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.99: Dorsalgia, unspecified (Gene-based burden) 2,029 European ancestry cases, 385,901 European ancestry controls NA Illumina [185344] 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90084497 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S82: Fracture of lower leg, including ankle 7,211 European ancestry cases, 374,121 European ancestry controls NA Affymetrix, Illumina [504964] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081029 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M62: Other disorders of muscle (Gene-based burden) 1,503 European ancestry cases, 383,520 European ancestry controls NA Illumina [185301] 0 muscular disease http://www.ebi.ac.uk/efo/EFO_0002970 GCST90084501 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R10.2: Pelvic and perineal pain 3,323 European ancestry cases, 378,082 European ancestry controls NA Affymetrix, Illumina [504929] 0 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90080786 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M62.8: Other specified disorders of muscle (Gene-based burden) 783 European ancestry cases, 386,702 European ancestry controls NA Illumina [185334] 0 muscular disease http://www.ebi.ac.uk/efo/EFO_0002970 GCST90084500 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79.890.: Hormone replacement therapy 1,698 European ancestry cases, 382,280 European ancestry controls NA Affymetrix, Illumina [504925] 0 hormone replacement therapy http://www.ebi.ac.uk/efo/EFO_0003961 GCST90081325 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65: Synovitis and tenosynovitis (Gene-based burden) 8,632 European ancestry cases, 371,813 European ancestry controls NA Illumina [185243] 0 tenosynovitis http://www.ebi.ac.uk/efo/EFO_1001435 GCST90084506 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R39.9: Unspecified symptoms and signs involving the genitourinary system 2,149 European ancestry cases, 379,294 European ancestry controls NA Affymetrix, Illumina [504915] 0 lower urinary tract symptom http://www.ebi.ac.uk/efo/EFO_0008008 GCST90080851 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 W55: Contact with other mammals 553 European ancestry cases, 386,361 European ancestry controls NA Affymetrix, Illumina [509758] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081131 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83.1: Varicose veins of lower extremities with inflammation (Gene-based burden) 594 European ancestry cases, 387,285 European ancestry controls NA Illumina [185344] 0 esophageal varices http://www.ebi.ac.uk/efo/EFO_0009545 GCST90084050 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E61: Deficiency of other nutrient elements 542 European ancestry cases, 386,428 European ancestry controls NA Affymetrix, Illumina [509752] 0 disorder of metabolite absorption and transport http://purl.obolibrary.org/obo/MONDO_0017757 GCST90079761 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I83.9: Asymptomatic varicose veins of lower extremities (Gene-based burden) 11,767 European ancestry cases, 376,048 European ancestry controls NA Illumina [185342] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90084051 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G54: Nerve root and plexus disorders 572 European ancestry cases, 386,268 European ancestry controls NA Affymetrix, Illumina [509752] 0 nerve plexus disease http://www.ebi.ac.uk/efo/EFO_0009559 GCST90079840 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84: Haemorrhoids (Gene-based burden) 27,106 European ancestry cases, 360,824 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084060 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R56.9: Unspecified convulsions 543 European ancestry cases, 386,355 European ancestry controls NA Affymetrix, Illumina [509749] 0 convulsion http://www.ebi.ac.uk/efo/EFO_0009853 GCST90080882 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.1: Internal haemorrhoids with other complications (Gene-based burden) 2,850 European ancestry cases, 385,080 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084053 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z75: Problems related to medical facilities and other health care 1,492 European ancestry cases, 385,407 European ancestry controls NA Affymetrix, Illumina [509749] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081321 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.2: Internal haemorrhoids without complication (Gene-based burden) 4,833 European ancestry cases, 383,097 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084054 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I48: Atrial fibrillation and flutter 20,107 European ancestry cases, 366,749 European ancestry controls 12,367 European ancestry cases, 93,153 European ancestry controls Affymetrix, Illumina [509720] 0 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90080015 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.4: External haemorrhoids with other complications (Gene-based burden) 534 European ancestry cases, 387,396 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084055 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M35: Other systemic involvement of connective tissue 3,379 European ancestry cases, 383,362 European ancestry controls NA Affymetrix, Illumina [509684] 0 connective tissue disease http://www.ebi.ac.uk/efo/EFO_1001986 GCST90080470 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.5: External haemorrhoids without complication (Gene-based burden) 1,062 European ancestry cases, 386,868 European ancestry controls NA Illumina [185344] 0 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90084056 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H44: Disorders of globe 646 European ancestry cases, 386,049 European ancestry controls NA Affymetrix, Illumina [509673] 0 eye disease http://www.ebi.ac.uk/efo/EFO_0003966 GCST90079913 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I84.6: Residual haemorrhoidal skin tags (Gene-based burden) 4,208 European ancestry cases, 383,722 European ancestry controls NA Illumina [185344] 0 Skin tags http://purl.obolibrary.org/obo/HP_0010609 GCST90084057 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.1: Localized swelling, mass and lump, neck 676 European ancestry cases, 386,074 European ancestry controls NA Affymetrix, Illumina [509669] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90080820 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.3: Trigger finger (Gene-based burden) 3,155 European ancestry cases, 384,623 European ancestry controls NA Illumina [185341] 0 stenosing tenosynovitis http://www.ebi.ac.uk/efo/EFO_0010822 GCST90084503 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.89: Encounter for other specified special examinations 2,191 European ancestry cases, 379,100 European ancestry controls NA Affymetrix, Illumina [504876] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081182 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.34: Trigger finger, ring finger (Gene-based burden) 1,114 European ancestry cases, 386,816 European ancestry controls NA Illumina [185344] 0 stenosing tenosynovitis http://www.ebi.ac.uk/efo/EFO_0010822 GCST90084502 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M17: Osteoarthritis of knee 26,780 European ancestry cases, 354,384 European ancestry controls NA Affymetrix, Illumina [504842] 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90080416 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.9: Synovitis and tenosynovitis, unspecified (Gene-based burden) 2,614 European ancestry cases, 385,133 European ancestry controls NA Illumina [185344] 0 pigmented villonodular synovitis http://www.ebi.ac.uk/efo/EFO_1001106 GCST90084505 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H00: Hordeolum and chalazion 4,139 European ancestry cases, 377,132 European ancestry controls NA Affymetrix, Illumina [504820] 0 hordeolum, meibomian cyst http://www.ebi.ac.uk/efo/EFO_0007315, http://www.ebi.ac.uk/efo/EFO_0007363 GCST90079863 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M65.96: Synovitis and tenosynovitis, unspecified (Gene-based burden) 944 European ancestry cases, 386,986 European ancestry controls NA Illumina [185344] 0 pigmented villonodular synovitis http://www.ebi.ac.uk/efo/EFO_1001106 GCST90084504 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H81: Disorders of vestibular function 3,343 European ancestry cases, 378,017 European ancestry controls NA Affymetrix, Illumina [504802] 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90079943 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M66: Spontaneous rupture of synovium and tendon (Gene-based burden) 802 European ancestry cases, 385,763 European ancestry controls NA Illumina [185320] 0 Tendon rupture http://purl.obolibrary.org/obo/HP_0100550 GCST90084507 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50: Poisoning by, adverse effect of and underdosing of diuretics and other and unspecified drugs, medicaments and biological substances 1,778 European ancestry cases, 379,361 European ancestry controls NA Affymetrix, Illumina [504711] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081061 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M67: Other disorders of synovium and tendon (Gene-based burden) 5,503 European ancestry cases, 375,456 European ancestry controls NA Illumina [185249] 0 tenosynovitis http://www.ebi.ac.uk/efo/EFO_1001435 GCST90084510 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S09.9: Unspecified injury of face and head 3,457 European ancestry cases, 377,561 European ancestry controls NA Affymetrix, Illumina [504660] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080954 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M67.4: Ganglion (Gene-based burden) 3,644 European ancestry cases, 381,796 European ancestry controls NA Illumina [185308] 0 ganglion http://purl.obolibrary.org/obo/UBERON_0000045 GCST90084508 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S09: Other and unspecified injuries of head 3,584 European ancestry cases, 377,427 European ancestry controls NA Affymetrix, Illumina [504658] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90080955 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M67.8: Other specified disorders of synovium and tendon (Gene-based burden) 697 European ancestry cases, 387,233 European ancestry controls NA Illumina [185344] 0 synovium disorder http://purl.obolibrary.org/obo/MONDO_0056799 GCST90084509 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78.4: Other and unspecified allergy 1,497 European ancestry cases, 379,554 European ancestry controls NA Affymetrix, Illumina [504638] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081065 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M70: Soft tissue disorders related to use, overuse and pressure (Gene-based burden) 5,010 European ancestry cases, 373,615 European ancestry controls NA Illumina [185183] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90084512 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H53: Visual disturbances 5,174 European ancestry cases, 375,749 European ancestry controls NA Affymetrix, Illumina [504624] 0 Abnormality of vision http://purl.obolibrary.org/obo/HP_0000504 GCST90079923 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M70.6: Trochanteric bursitis (Gene-based burden) 904 European ancestry cases, 387,026 European ancestry controls NA Illumina [185344] 0 bursitis http://purl.obolibrary.org/obo/MONDO_0002471 GCST90084511 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L50: Urticaria 2,279 European ancestry cases, 378,852 European ancestry controls NA Affymetrix, Illumina [504606] 0 urticaria http://www.ebi.ac.uk/efo/EFO_0005531 GCST90080352 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M71: Other bursopathies (Gene-based burden) 1,374 European ancestry cases, 384,525 European ancestry controls NA Illumina [185306] 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90084514 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T78.40: Allergy, unspecified 1,044 European ancestry cases, 379,975 European ancestry controls NA Affymetrix, Illumina [504595] 0 adverse effect http://www.ebi.ac.uk/efo/EFO_0009658 GCST90081064 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I86: Varicose veins of other sites (Gene-based burden) 766 European ancestry cases, 386,186 European ancestry controls NA Illumina [185325] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90084063 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G47.9: Sleep disorder, unspecified 1,314 European ancestry cases, 385,409 European ancestry controls NA Affymetrix, Illumina [509653] 0 Sleep Disorder http://www.ebi.ac.uk/efo/EFO_0008568 GCST90079834 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I87: Other disorders of veins (Gene-based burden) 687 European ancestry cases, 386,724 European ancestry controls NA Illumina [185335] 0 vascular disease http://www.ebi.ac.uk/efo/EFO_0004264 GCST90084064 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H73: Other disorders of tympanic membrane 786 European ancestry cases, 385,979 European ancestry controls NA Affymetrix, Illumina [509652] 0 tympanic membrane disease http://www.ebi.ac.uk/efo/EFO_0009570 GCST90079940 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I89: Other noninfective disorders of lymphatic vessels and lymph nodes (Gene-based burden) 1,174 European ancestry cases, 385,860 European ancestry controls NA Illumina [185332] 0 lymphatic system disease http://www.ebi.ac.uk/efo/EFO_0007352 GCST90084066 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73.9: Hyperglycemia, unspecified 899 European ancestry cases, 385,804 European ancestry controls NA Affymetrix, Illumina [509646] 0 Hyperglycemia http://purl.obolibrary.org/obo/HP_0003074 GCST90080905 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I89.0: Lymphedema, not elsewhere classified (Gene-based burden) 766 European ancestry cases, 386,832 European ancestry controls NA Illumina [185343] 0 primary lymphedema http://purl.obolibrary.org/obo/MONDO_0019175 GCST90084065 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R93.8: Abnormal findings on diagnostic imaging of other specified body structures 687 European ancestry cases, 386,003 European ancestry controls NA Affymetrix, Illumina [509634] 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90080932 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I95: Hypotension (Gene-based burden) 7,547 European ancestry cases, 378,733 European ancestry controls NA Illumina [185316] 0 hypotension http://www.ebi.ac.uk/efo/EFO_0005251 GCST90084069 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S76: Injury of muscle, fascia and tendon at hip and thigh level 547 European ancestry cases, 386,228 European ancestry controls NA Affymetrix, Illumina [509627] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081014 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I95.1: Orthostatic hypotension (Gene-based burden) 2,084 European ancestry cases, 385,821 European ancestry controls NA Illumina [185343] 0 orthostatic hypotension http://www.ebi.ac.uk/efo/EFO_0005252 GCST90084067 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E16: Other disorders of pancreatic internal secretion 1,620 European ancestry cases, 385,084 European ancestry controls NA Affymetrix, Illumina [509624] 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90079750 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I95.9: Hypotension, unspecified (Gene-based burden) 5,127 European ancestry cases, 382,771 European ancestry controls NA Illumina [185343] 0 hypotension http://www.ebi.ac.uk/efo/EFO_0005251 GCST90084068 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I21: Acute myocardial infarction 10,907 European ancestry cases, 375,797 European ancestry controls NA Affymetrix, Illumina [509622] 0 acute myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008583 GCST90079973 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J00: Acute nasopharyngitis [common cold] (Gene-based burden) 2,558 European ancestry cases, 377,078 European ancestry controls NA Illumina [185209] 0 common cold http://www.ebi.ac.uk/efo/EFO_0007214 GCST90084070 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J33: Nasal polyp 4,168 European ancestry cases, 382,509 European ancestry controls NA Affymetrix, Illumina [509622] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90080113 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J01: Acute sinusitis (Gene-based burden) 7,767 European ancestry cases, 366,131 European ancestry controls NA Illumina [185104] 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90084071 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z97.8: Presence of other specified devices 1,814 European ancestry cases, 384,875 European ancestry controls NA Affymetrix, Illumina [509621] 0 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90081433 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J02: Acute pharyngitis (Gene-based burden) 10,891 European ancestry cases, 351,064 European ancestry controls NA Illumina [184891] 0 acute pharyngitis http://www.ebi.ac.uk/efo/EFO_0009657 GCST90084073 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13.6: Other specified diabetes mellitus with other specified complications 8,624 European ancestry cases, 378,107 European ancestry controls 134 European ancestry cases, 108,331 European ancestry controls Affymetrix, Illumina [509614] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90079745 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J02.9: Acute pharyngitis, unspecified (Gene-based burden) 6,744 European ancestry cases, 365,218 European ancestry controls NA Illumina [185076] 0 acute pharyngitis http://www.ebi.ac.uk/efo/EFO_0009657 GCST90084072 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13.62: Other specified diabetes mellitus with skin complications 8,622 European ancestry cases, 378,109 European ancestry controls NA Affymetrix, Illumina [509614] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90079744 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J03: Acute tonsillitis (Gene-based burden) 2,733 European ancestry cases, 376,762 European ancestry controls NA Illumina [185167] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90084075 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E13.621.: Other specified diabetes mellitus with foot ulcer 8,622 European ancestry cases, 378,109 European ancestry controls NA Affymetrix, Illumina [509614] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90079743 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J03.9: Acute tonsillitis, unspecified (Gene-based burden) 942 European ancestry cases, 384,892 European ancestry controls NA Illumina [185302] 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90084074 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H11: Other disorders of conjunctiva 1,714 European ancestry cases, 380,389 European ancestry controls NA Affymetrix, Illumina [505596] 0 Conjunctival Disorder http://www.ebi.ac.uk/efo/EFO_1000203 GCST90079881 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48: Other spondylopathies (Gene-based burden) 5,848 European ancestry cases, 381,138 European ancestry controls NA Illumina [185328] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90084476 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R11.103.11: Vomiting 15,689 European ancestry cases, 366,456 European ancestry controls NA Affymetrix, Illumina [505581] 0 Vomiting http://purl.obolibrary.org/obo/HP_0002013 GCST90080794 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48.0: Spinal stenosis (Gene-based burden) 5,125 European ancestry cases, 382,789 European ancestry controls NA Illumina [185344] 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90084475 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R79: Other abnormal findings of blood chemistry 11,799 European ancestry cases, 370,234 European ancestry controls NA Affymetrix, Illumina [505546] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080911 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48.02: Spinal stenosis, cervical region (Gene-based burden) 607 European ancestry cases, 387,323 European ancestry controls NA Illumina [185344] 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90084473 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L85.3: Xerosis cutis 964 European ancestry cases, 381,055 European ancestry controls NA Affymetrix, Illumina [505442] 0 Dry skin http://purl.obolibrary.org/obo/HP_0000958 GCST90080371 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M48.06: Spinal stenosis, lumbar region (Gene-based burden) 3,396 European ancestry cases, 384,534 European ancestry controls NA Illumina [185344] 0 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90084474 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93.4: Sprain of ankle 1,060 European ancestry cases, 380,874 European ancestry controls NA Affymetrix, Illumina [505437] 0 sprain http://www.ebi.ac.uk/efo/EFO_0009582 GCST90081042 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50: Cervical disc disorders (Gene-based burden) 2,103 European ancestry cases, 384,499 European ancestry controls NA Illumina [185308] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90084480 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.1: Generalized anxiety disorder 2,967 European ancestry cases, 378,840 European ancestry controls NA Affymetrix, Illumina [505403] 0 generalized anxiety disorder http://www.ebi.ac.uk/efo/EFO_1001892 GCST90079809 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50.0: Cervical disc disorder with myelopathy (Gene-based burden) 505 European ancestry cases, 387,385 European ancestry controls NA Illumina [185343] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90084477 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z30.41: Encounter for surveillance of contraceptive pills 616 European ancestry cases, 386,850 European ancestry controls NA Affymetrix, Illumina [505400] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081236 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50.1: Cervical disc disorder with radiculopathy (Gene-based burden) 642 European ancestry cases, 387,203 European ancestry controls NA Illumina [185343] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90084478 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S33: Dislocation and sprain of joints and ligaments of lumbar spine and pelvis 1,020 European ancestry cases, 380,769 European ancestry controls NA Affymetrix, Illumina [505392] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080972 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M50.3: Other cervical disc degeneration (Gene-based burden) 516 European ancestry cases, 387,414 European ancestry controls NA Illumina [185344] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90084479 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z79: Long term (current) drug therapy 5,865 European ancestry cases, 375,980 European ancestry controls NA Affymetrix, Illumina [505384] 0 treatment http://www.ebi.ac.uk/efo/EFO_0000727 GCST90081328 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51: Thoracic, thoracolumbar, and lumbosacral intervertebral disc disorders (Gene-based burden) 10,022 European ancestry cases, 373,202 European ancestry controls NA Illumina [185270] 0 discitis http://www.ebi.ac.uk/efo/EFO_1000900 GCST90084484 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.3: Encounter for examination of blood pressure 152,936 European ancestry cases, 228,996 European ancestry controls NA Affymetrix, Illumina [505381] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081180 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51.1: Thoracic, thoracolumbar and lumbosacral intervertebral disc disorders with radiculopathy (Gene-based burden) 4,203 European ancestry cases, 383,475 European ancestry controls NA Illumina [185331] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90084481 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50.9: Poisoning by, adverse effect of and underdosing of other and unspecified drugs, medicaments and biological substances 1,659 European ancestry cases, 380,109 European ancestry controls NA Affymetrix, Illumina [505311] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081060 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51.2: Other thoracic, thoracolumbar and lumbosacral intervertebral disc displacement (Gene-based burden) 3,205 European ancestry cases, 384,725 European ancestry controls NA Illumina [185344] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90084482 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 T50.90: Poisoning by, adverse effect of and underdosing of unspecified drugs, medicaments and biological substances 1,366 European ancestry cases, 380,369 European ancestry controls NA Affymetrix, Illumina [505267] 0 poisoning http://www.ebi.ac.uk/efo/EFO_0008546 GCST90081059 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M51.3: Other thoracic, thoracolumbar and lumbosacral intervertebral disc degeneration (Gene-based burden) 3,288 European ancestry cases, 384,639 European ancestry controls NA Illumina [185344] 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90084483 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H43: Disorders of vitreous body 3,002 European ancestry cases, 378,726 European ancestry controls NA Affymetrix, Illumina [505256] 0 vitreous body disease http://www.ebi.ac.uk/efo/EFO_0008624 GCST90079912 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M43.1: Spondylolisthesis (Gene-based burden) 1,786 European ancestry cases, 385,893 European ancestry controls NA Illumina [185339] 0 spondylolisthesis http://www.ebi.ac.uk/efo/EFO_0007493 GCST90084460 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R45: Symptoms and signs involving emotional state 2,300 European ancestry cases, 380,293 European ancestry controls NA Affymetrix, Illumina [505895] 0 sign or symptom http://www.ebi.ac.uk/efo/EFO_0003765 GCST90080861 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M43.16: Spondylolisthesis, lumbar region (Gene-based burden) 1,184 European ancestry cases, 386,746 European ancestry controls NA Illumina [185344] 0 spondylolisthesis http://www.ebi.ac.uk/efo/EFO_0007493 GCST90084459 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R14: Flatulence and related conditions 3,601 European ancestry cases, 378,807 European ancestry controls NA Affymetrix, Illumina [505835] 0 flatulence http://www.ebi.ac.uk/efo/EFO_0009669 GCST90080802 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M46: Other inflammatory spondylopathies (Gene-based burden) 1,991 European ancestry cases, 384,956 European ancestry controls NA Illumina [185326] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90084463 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L71: Rosacea 4,002 European ancestry cases, 378,283 European ancestry controls NA Affymetrix, Illumina [505833] 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90080360 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M46.9: Unspecified inflammatory spondylopathy (Gene-based burden) 1,437 European ancestry cases, 386,493 European ancestry controls NA Illumina [185344] 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90084462 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R79.89: Other specified abnormal findings of blood chemistry 3,082 European ancestry cases, 379,295 European ancestry controls NA Affymetrix, Illumina [505812] 0 test result http://www.ebi.ac.uk/efo/EFO_0000720 GCST90080909 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47: Spondylosis (Gene-based burden) 13,192 European ancestry cases, 364,110 European ancestry controls NA Illumina [185186] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084472 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G56: Mononeuropathies of upper limb 13,929 European ancestry cases, 368,599 European ancestry controls NA Affymetrix, Illumina [505810] 0 mononeuropathy http://www.ebi.ac.uk/efo/EFO_0009558 GCST90079846 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.2: Other spondylosis with radiculopathy (Gene-based burden) 761 European ancestry cases, 387,169 European ancestry controls NA Illumina [185344] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084464 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F41.9: Anxiety disorder, unspecified 9,404 European ancestry cases, 372,895 European ancestry controls NA Affymetrix, Illumina [505789] 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90079811 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.8: Other spondylosis (Gene-based burden) 6,258 European ancestry cases, 381,603 European ancestry controls NA Illumina [185343] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084468 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22.9: Localized swelling, mass and lump, unspecified 1,032 European ancestry cases, 381,474 European ancestry controls NA Affymetrix, Illumina [505772] 0 localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0010683 GCST90080822 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.80: Other spondylosis (Gene-based burden) 503 European ancestry cases, 387,427 European ancestry controls NA Illumina [185344] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084465 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H10.9: Unspecified conjunctivitis 1,400 European ancestry cases, 380,794 European ancestry controls NA Affymetrix, Illumina [505712] 0 conjunctivitis http://www.ebi.ac.uk/efo/EFO_0009450 GCST90079879 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.82: Other spondylosis (Gene-based burden) 2,593 European ancestry cases, 385,337 European ancestry controls NA Illumina [185344] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084466 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S92: Fracture of foot and toe, except ankle 1,806 European ancestry cases, 380,162 European ancestry controls NA Affymetrix, Illumina [505641] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90081039 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.86: Other spondylosis (Gene-based burden) 1,930 European ancestry cases, 386,000 European ancestry controls NA Illumina [185344] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084467 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.89: Encounter for screening for other disorder 1,891 European ancestry cases, 380,370 European ancestry controls NA Affymetrix, Illumina [505618] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081217 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.9: Spondylosis, unspecified (Gene-based burden) 4,418 European ancestry cases, 382,756 European ancestry controls NA Illumina [185326] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084471 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93.40: Sprain of unspecified ligament of ankle 900 European ancestry cases, 381,230 European ancestry controls NA Affymetrix, Illumina [505605] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081041 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.92: Spondylosis, unspecified (Gene-based burden) 893 European ancestry cases, 387,037 European ancestry controls NA Illumina [185344] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084469 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S93.409.: Sprain of unspecified ligament of unspecified ankle 899 European ancestry cases, 381,231 European ancestry controls NA Affymetrix, Illumina [505605] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081040 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47.96: Spondylosis, unspecified (Gene-based burden) 955 European ancestry cases, 386,975 European ancestry controls NA Illumina [185344] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90084470 Exome-wide sequencing 2021-05-20 33069728 Pu W 2020-10-15 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/33069728 Exome-wide association analysis suggests LRP2BP as a susceptibility gene for endothelial injury in systemic sclerosis in Han Chinese population. Systemic sclerosis 527 Han Chinese ancestry cases, 5,024 Han Chinese ancestry controls 479 Han Chinese ancestry cases, 1,096 Han Chinese ancestry controls Illumina [84228] 4 systemic scleroderma http://www.ebi.ac.uk/efo/EFO_0000717 GCST011709 Exome genotyping array [Exome array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K08: Other disorders of teeth and supporting structures 3,287 European ancestry cases, 382,909 European ancestry controls NA Affymetrix, Illumina [509118] 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90080174 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K11: Diseases of salivary glands (Gene-based burden) 1,546 European ancestry cases, 384,408 European ancestry controls NA Illumina [185312] 0 salivary gland disease http://www.ebi.ac.uk/efo/EFO_0008581 GCST90084163 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 P29: Cardiovascular disorders originating in the perinatal period 1,855 European ancestry cases, 384,135 European ancestry controls NA Affymetrix, Illumina [509114] 0 cardiovascular disease, pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0000319, http://www.ebi.ac.uk/efo/EFO_0009682 GCST90080746 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K12: Stomatitis and related lesions (Gene-based burden) 1,778 European ancestry cases, 382,114 European ancestry controls NA Illumina [185280] 0 stomatitis http://www.ebi.ac.uk/efo/EFO_0009688 GCST90084165 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.69: Personal history of other diseases of the nervous system and sense organs 1,115 European ancestry cases, 385,013 European ancestry controls NA Affymetrix, Illumina [509087] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081361 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K12.1: Other forms of stomatitis (Gene-based burden) 770 European ancestry cases, 385,531 European ancestry controls NA Illumina [185318] 0 stomatitis http://www.ebi.ac.uk/efo/EFO_0009688 GCST90084164 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R01: Cardiac murmurs and other cardiac sounds 1,620 European ancestry cases, 384,413 European ancestry controls NA Affymetrix, Illumina [509083] 0 Heart murmur http://purl.obolibrary.org/obo/HP_0030148 GCST90080756 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K13: Other diseases of lip and oral mucosa (Gene-based burden) 3,921 European ancestry cases, 381,774 European ancestry controls NA Illumina [185304] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90084168 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J39: Other diseases of upper respiratory tract 1,109 European ancestry cases, 384,982 European ancestry controls NA Affymetrix, Illumina [509082] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90080124 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K13.0: Diseases of lips (Gene-based burden) 824 European ancestry cases, 387,005 European ancestry controls NA Illumina [185340] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90084166 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Type 2 diabetes New 30,259 European ancestry cases, 355,886 European ancestry controls 29,639 European ancestry cases, 91,572 European ancestry controls Affymetrix, Illumina [509075] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90081516 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K13.7: Other and unspecified lesions of oral mucosa (Gene-based burden) 2,223 European ancestry cases, 385,531 European ancestry controls NA Illumina [185343] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90084167 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.0: Intra-abdominal and pelvic swelling, mass and lump 1,552 European ancestry cases, 384,513 European ancestry controls NA Affymetrix, Illumina [509056] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90080808 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K14: Diseases of tongue (Gene-based burden) 1,808 European ancestry cases, 384,676 European ancestry controls NA Illumina [185307] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90084170 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z88.0: Allergy status to penicillin 20,233 European ancestry cases, 365,807 European ancestry controls 605 European ancestry cases, 33,940 European ancestry controls Affymetrix, Illumina [509056] 0 allergic disease http://purl.obolibrary.org/obo/MONDO_0005271 GCST90081381 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K14.8: Other diseases of tongue (Gene-based burden) 866 European ancestry cases, 387,037 European ancestry controls NA Illumina [185342] 0 mouth disease http://www.ebi.ac.uk/efo/EFO_1001047 GCST90084169 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M06: Other rheumatoid arthritis 6,100 European ancestry cases, 379,952 European ancestry controls NA Affymetrix, Illumina [509054] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90080392 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K20: Esophagitis (Gene-based burden) 12,056 European ancestry cases, 371,916 European ancestry controls NA Illumina [185296] 0 Esophagitis http://purl.obolibrary.org/obo/HP_0100633 GCST90084171 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S22: Fracture of rib(s), sternum and thoracic spine 2,628 European ancestry cases, 383,401 European ancestry controls NA Affymetrix, Illumina [509050] 0 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90080963 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21: Gastro-esophageal reflux disease (Gene-based burden) 34,552 European ancestry cases, 342,096 European ancestry controls NA Illumina [185198] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90084174 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L90: Atrophic disorders of skin 3,987 European ancestry cases, 382,110 European ancestry controls NA Affymetrix, Illumina [509047] 0 skin atrophy http://www.ebi.ac.uk/efo/EFO_1000766 GCST90080377 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21.0: Gastro-esophageal reflux disease with esophagitis (Gene-based burden) 12,871 European ancestry cases, 375,044 European ancestry controls NA Illumina [185344] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90084172 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H52: Disorders of refraction and accommodation 2,691 European ancestry cases, 383,414 European ancestry controls NA Affymetrix, Illumina [509026] 0 Abnormality of refraction http://purl.obolibrary.org/obo/HP_0000539 GCST90079917 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K21.9: Gastro-esophageal reflux disease without esophagitis (Gene-based burden) 22,340 European ancestry cases, 359,319 European ancestry controls NA Illumina [185271] 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90084173 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R63.4: Abnormal weight loss 7,833 European ancestry cases, 378,297 European ancestry controls NA Affymetrix, Illumina [509022] 0 body weight loss http://www.ebi.ac.uk/efo/EFO_0005245 GCST90080894 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N52: Male erectile dysfunction 6,768 European ancestry cases, 372,688 European ancestry controls NA Affymetrix, Illumina [503036] 0 erectile dysfunction http://www.ebi.ac.uk/efo/EFO_0004234 GCST90080637 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N23: Unspecified renal colic (Gene-based burden) 2,723 European ancestry cases, 382,722 European ancestry controls NA Illumina [185323] 0 renal colic http://www.ebi.ac.uk/efo/EFO_1001412 GCST90084577 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H04: Disorders of lacrimal system 5,367 European ancestry cases, 373,770 European ancestry controls NA Affymetrix, Illumina [503013] 0 lacrimal apparatus disease http://www.ebi.ac.uk/efo/EFO_0009455 GCST90079878 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28: Other disorders of kidney and ureter, not elsewhere classified (Gene-based burden) 3,413 European ancestry cases, 383,589 European ancestry controls NA Illumina [185328] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90084581 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L08.9: Local infection of the skin and subcutaneous tissue, unspecified 3,110 European ancestry cases, 376,282 European ancestry controls NA Affymetrix, Illumina [502997] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90080335 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28.1: Cyst of kidney, acquired (Gene-based burden) 1,824 European ancestry cases, 386,102 European ancestry controls NA Illumina [185344] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90084578 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z82.5: Family history of asthma and other chronic lower respiratory diseases 2,054 European ancestry cases, 377,121 European ancestry controls NA Affymetrix, Illumina [502932] 0 family history http://www.ebi.ac.uk/efo/EFO_0000493 GCST90081338 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28.8: Other specified disorders of kidney and ureter (Gene-based burden) 830 European ancestry cases, 387,074 European ancestry controls NA Illumina [185344] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90084579 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H66: Suppurative and unspecified otitis media 3,333 European ancestry cases, 375,772 European ancestry controls NA Affymetrix, Illumina [502921] 0 suppurative otitis media http://www.ebi.ac.uk/efo/EFO_0007503 GCST90079935 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N28.9: Disorder of kidney and ureter, unspecified (Gene-based burden) 742 European ancestry cases, 386,838 European ancestry controls NA Illumina [185339] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90084580 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z63.4: Disappearance and death of family member 2,457 European ancestry cases, 376,692 European ancestry controls NA Affymetrix, Illumina [502910] 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90081300 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30: Cystitis (Gene-based burden) 7,658 European ancestry cases, 372,291 European ancestry controls NA Illumina [185209] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90084585 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M54.30: Sciatica, unspecified side 3,519 European ancestry cases, 375,578 European ancestry controls NA Affymetrix, Illumina [502908] 0 Sciatica http://purl.obolibrary.org/obo/HP_0011868 GCST90080503 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30.2: Other chronic cystitis (Gene-based burden) 763 European ancestry cases, 387,152 European ancestry controls NA Illumina [185344] 0 chronic cystitis http://www.ebi.ac.uk/efo/EFO_1000023 GCST90084582 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R00.2: Palpitations 9,306 European ancestry cases, 369,733 European ancestry controls NA Affymetrix, Illumina [502897] 0 Palpitations http://purl.obolibrary.org/obo/HP_0001962 GCST90080752 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30.8: Other cystitis (Gene-based burden) 753 European ancestry cases, 387,172 European ancestry controls NA Illumina [185344] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90084583 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K59.00: Constipation, unspecified 3,370 European ancestry cases, 375,690 European ancestry controls NA Affymetrix, Illumina [502862] 0 constipation disorder http://purl.obolibrary.org/obo/MONDO_0002203 GCST90080253 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N30.9: Cystitis, unspecified (Gene-based burden) 1,711 European ancestry cases, 386,207 European ancestry controls NA Illumina [185344] 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90084584 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86: Personal history of certain other diseases 68,491 European ancestry cases, 310,419 European ancestry controls NA Affymetrix, Illumina [502846] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081365 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N31: Neuromuscular dysfunction of bladder, not elsewhere classified (Gene-based burden) 2,404 European ancestry cases, 383,356 European ancestry controls NA Illumina [185321] 0 Neurogenic bladder http://purl.obolibrary.org/obo/HP_0000011 GCST90084588 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.9: Osteoarthritis, unspecified site 23,959 European ancestry cases, 354,957 European ancestry controls NA Affymetrix, Illumina [502770] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080426 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N31.8: Other neuromuscular dysfunction of bladder (Gene-based burden) 866 European ancestry cases, 387,064 European ancestry controls NA Illumina [185344] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90084586 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J11: Influenza due to unidentified influenza virus 1,922 European ancestry cases, 377,148 European ancestry controls NA Affymetrix, Illumina [502728] 0 influenza http://www.ebi.ac.uk/efo/EFO_0007328 GCST90080093 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N31.9: Neuromuscular dysfunction of bladder, unspecified (Gene-based burden) 816 European ancestry cases, 387,114 European ancestry controls NA Illumina [185344] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90084587 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R73: Elevated blood glucose level 4,283 European ancestry cases, 374,702 European ancestry controls NA Affymetrix, Illumina [502720] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90080906 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S60: Superficial injury of wrist, hand and fingers 652 European ancestry cases, 385,604 European ancestry controls NA Affymetrix, Illumina [509260] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90080992 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J93: Pneumothorax and air leak (Gene-based burden) 1,190 European ancestry cases, 386,185 European ancestry controls NA Illumina [185328] 0 pneumothorax http://purl.obolibrary.org/obo/MONDO_0002076 GCST90084139 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J44: Other chronic obstructive pulmonary disease 12,856 European ancestry cases, 373,496 European ancestry controls NA Affymetrix, Illumina [509259] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90080133 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J93.9: Pneumothorax, unspecified (Gene-based burden) 837 European ancestry cases, 387,093 European ancestry controls NA Illumina [185344] 0 pneumothorax http://purl.obolibrary.org/obo/MONDO_0002076 GCST90084138 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I25.9: Chronic ischemic heart disease, unspecified 17,106 European ancestry cases, 369,135 European ancestry controls 5,879 European ancestry cases, 96,213 European ancestry controls Affymetrix, Illumina [509258] 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90079981 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J95: Intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified (Gene-based burden) 523 European ancestry cases, 387,401 European ancestry controls NA Illumina [185344] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084140 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 I95: Hypotension 7,547 European ancestry cases, 378,733 European ancestry controls NA Affymetrix, Illumina [509256] 0 hypotension http://www.ebi.ac.uk/efo/EFO_0005251 GCST90080083 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J96: Respiratory failure, not elsewhere classified (Gene-based burden) 3,157 European ancestry cases, 384,744 European ancestry controls NA Illumina [185344] 0 respiratory failure http://www.ebi.ac.uk/efo/EFO_0009686 GCST90084143 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L43: Lichen planus 1,295 European ancestry cases, 385,047 European ancestry controls NA Affymetrix, Illumina [509247] 0 lichen planus http://www.ebi.ac.uk/efo/EFO_1000726 GCST90080351 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J96.0: Acute respiratory failure (Gene-based burden) 503 European ancestry cases, 387,427 European ancestry controls NA Illumina [185344] 0 acute respiratory failure http://purl.obolibrary.org/obo/MONDO_0001208 GCST90084141 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32: Other disorders of bladder 10,863 European ancestry cases, 375,390 European ancestry controls NA Affymetrix, Illumina [509236] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90080607 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J96.9: Respiratory failure, unspecified (Gene-based burden) 2,652 European ancestry cases, 385,269 European ancestry controls NA Illumina [185344] 0 respiratory failure http://www.ebi.ac.uk/efo/EFO_0009686 GCST90084142 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K44.9: Diaphragmatic hernia without obstruction or gangrene 34,283 European ancestry cases, 352,048 European ancestry controls NA Affymetrix, Illumina [509228] 0 diaphragmatic hernia http://www.ebi.ac.uk/efo/EFO_0008561 GCST90080227 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.1: Pulmonary collapse (Gene-based burden) 3,065 European ancestry cases, 384,755 European ancestry controls NA Illumina [185337] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084144 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 H16: Keratitis 704 European ancestry cases, 385,576 European ancestry controls NA Affymetrix, Illumina [509226] 0 keratitis http://www.ebi.ac.uk/efo/EFO_0009449 GCST90079882 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.4: Other disorders of lung (Gene-based burden) 1,268 European ancestry cases, 386,643 European ancestry controls NA Illumina [185344] 0 lung disease http://www.ebi.ac.uk/efo/EFO_0003818 GCST90084146 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M79.8: Other specified soft tissue disorders 6,170 European ancestry cases, 380,041 European ancestry controls NA Affymetrix, Illumina [509224] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080553 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.457.6: Other disorders of lung (Gene-based burden) 20,378 European ancestry cases, 357,232 European ancestry controls NA Illumina [185160] 0 lung disease http://www.ebi.ac.uk/efo/EFO_0003818 GCST90084145 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K12.1: Other forms of stomatitis 770 European ancestry cases, 385,531 European ancestry controls NA Affymetrix, Illumina [509219] 0 stomatitis http://www.ebi.ac.uk/efo/EFO_0009688 GCST90080178 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.9: Respiratory disorder, unspecified (Gene-based burden) 14,771 European ancestry cases, 367,671 European ancestry controls NA Illumina [185225] 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90084147 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M23: Internal derangement of knee 17,668 European ancestry cases, 368,598 European ancestry controls NA Affymetrix, Illumina [509216] 0 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90080447 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K01: Embedded and impacted teeth (Gene-based burden) 2,066 European ancestry cases, 385,580 European ancestry controls NA Illumina [185341] 0 Impacted tooth http://purl.obolibrary.org/obo/HP_0011079 GCST90084149 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F33: Major depressive disorder, recurrent 1,721 European ancestry cases, 384,459 European ancestry controls NA Affymetrix, Illumina [509212] 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90079805 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K01.1: Impacted teeth (Gene-based burden) 1,967 European ancestry cases, 385,963 European ancestry controls NA Illumina [185344] 0 Impacted tooth http://purl.obolibrary.org/obo/HP_0011079 GCST90084148 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S80: Superficial injury of knee and lower leg 1,159 European ancestry cases, 385,152 European ancestry controls NA Affymetrix, Illumina [509203] 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90081016 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J92: Pleural plaque (Gene-based burden) 1,162 European ancestry cases, 386,480 European ancestry controls NA Illumina [185342] 0 pleural disorder http://purl.obolibrary.org/obo/MONDO_0002037 GCST90084137 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E53: Deficiency of other B group vitamins 1,552 European ancestry cases, 384,821 European ancestry controls NA Affymetrix, Illumina [509288] 0 disorder of other vitamins and cofactors metabolism and transport http://purl.obolibrary.org/obo/MONDO_0017760 GCST90079758 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J92.0: Pleural plaque with presence of asbestos (Gene-based burden) 573 European ancestry cases, 387,357 European ancestry controls NA Illumina [185343] 0 pleural disorder http://purl.obolibrary.org/obo/MONDO_0002037 GCST90084135 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R01.1: Cardiac murmur, unspecified 1,507 European ancestry cases, 384,754 European ancestry controls NA Affymetrix, Illumina [509268] 0 Heart murmur http://purl.obolibrary.org/obo/HP_0030148 GCST90080755 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R06.0: Dyspnea 15,391 European ancestry cases, 362,721 European ancestry controls NA Affymetrix, Illumina [502129] 0 Dyspnea http://purl.obolibrary.org/obo/HP_0002094 GCST90080767 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.8: Other specified disorders of urinary system (Gene-based burden) 580 European ancestry cases, 387,349 European ancestry controls NA Illumina [185344] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90084600 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L57: Skin changes due to chronic exposure to nonionizing radiation 7,797 European ancestry cases, 370,171 European ancestry controls NA Affymetrix, Illumina [502075] 0 radiation-induced disorder http://www.ebi.ac.uk/efo/EFO_0009565 GCST90080355 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.9: Disorder of urinary system, unspecified (Gene-based burden) 688 European ancestry cases, 387,084 European ancestry controls NA Illumina [185342] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90084601 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z80: Family history of primary malignant neoplasm 13,831 European ancestry cases, 364,232 European ancestry controls 10,044 European ancestry cases, 33,532 European ancestry controls Affymetrix, Illumina [501971] 0 family history of cancer http://www.ebi.ac.uk/efo/EFO_0009640 GCST90081334 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N40: Benign prostatic hyperplasia (Gene-based burden) 15,936 European ancestry cases, 156,384 European ancestry controls NA Illumina [175258] 0 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90084603 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 F32.9: Major depressive disorder, single episode, unspecified 22,358 European ancestry cases, 355,688 European ancestry controls NA Affymetrix, Illumina [501950] 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90079803 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N41: Inflammatory diseases of prostate (Gene-based burden) 2,279 European ancestry cases, 172,873 European ancestry controls NA Illumina [175517] 0 prostatitis http://www.ebi.ac.uk/efo/EFO_0003830 GCST90084606 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Phosphate levels (UKB data field 30810) 377,669 European ancestry individuals 30,361 European ancestry individuals Affymetrix, Illumina [501882] 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90079037 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N41.1: Chronic prostatitis (Gene-based burden) 1,070 European ancestry cases, 193,535 European ancestry controls NA Illumina [177570] 0 prostatitis http://www.ebi.ac.uk/efo/EFO_0003830 GCST90084604 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z01.8: Encounter for other specified special examinations 5,418 European ancestry cases, 372,494 European ancestry controls NA Affymetrix, Illumina [501727] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081183 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N41.9: Inflammatory disease of prostate, unspecified (Gene-based burden) 712 European ancestry cases, 193,893 European ancestry controls NA Illumina [177570] 0 inflammatory disease http://www.ebi.ac.uk/efo/EFO_0009903 GCST90084605 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J98.457.6: Other disorders of lung 20,378 European ancestry cases, 357,232 European ancestry controls NA Affymetrix, Illumina [501683] 0 lung disease http://www.ebi.ac.uk/efo/EFO_0003818 GCST90080159 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N42: Other and unspecified disorders of prostate (Gene-based burden) 1,670 European ancestry cases, 174,103 European ancestry controls NA Illumina [175574] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90084608 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R82.998.: Other and unspecified abnormal findings in urine 5,824 European ancestry cases, 371,752 European ancestry controls NA Affymetrix, Illumina [501634] 0 Abnormality of urine homeostasis http://purl.obolibrary.org/obo/HP_0003110 GCST90080915 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N42.8: Other specified disorders of prostate (Gene-based burden) 736 European ancestry cases, 175,360 European ancestry controls NA Illumina [175602] 0 prostate disease http://www.ebi.ac.uk/efo/EFO_0009602 GCST90084607 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M47: Spondylosis 13,192 European ancestry cases, 364,110 European ancestry controls NA Affymetrix, Illumina [501622] 0 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90080486 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N43: Hydrocele and spermatocele (Gene-based burden) 1,816 European ancestry cases, 173,556 European ancestry controls NA Illumina [175555] 0 testicular hydrocele, spermatocele http://www.ebi.ac.uk/efo/EFO_1001859, http://www.ebi.ac.uk/efo/EFO_1001189 GCST90084610 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K58: Irritable bowel syndrome 11,224 European ancestry cases, 366,402 European ancestry controls NA Affymetrix, Illumina [501618] 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90080252 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N43.3: Hydrocele, unspecified (Gene-based burden) 1,572 European ancestry cases, 193,033 European ancestry controls NA Illumina [177570] 0 testicular hydrocele http://www.ebi.ac.uk/efo/EFO_1001859 GCST90084609 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J92.9: Pleural plaque without asbestos (Gene-based burden) 668 European ancestry cases, 387,262 European ancestry controls NA Illumina [185208] 0 pleural disorder http://purl.obolibrary.org/obo/MONDO_0002037 GCST90084136 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32: Other disorders of bladder (Gene-based burden) 10,863 European ancestry cases, 375,390 European ancestry controls NA Illumina [185324] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90084593 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L20: Atopic dermatitis 2,972 European ancestry cases, 375,981 European ancestry controls 1,810 European ancestry cases, 108,305 European ancestry controls Affymetrix, Illumina [502637] 0 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90080337 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.0: Bladder-neck obstruction (Gene-based burden) 2,303 European ancestry cases, 385,191 European ancestry controls NA Illumina [185339] 0 bladder neck obstruction http://www.ebi.ac.uk/efo/EFO_1000840 GCST90084589 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Albumin levels (UKB data field 30600) 378,401 European ancestry individuals 108,913 European ancestry individuals Affymetrix, Illumina [502523] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90079012 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.3: Diverticulum of bladder (Gene-based burden) 1,020 European ancestry cases, 386,910 European ancestry controls NA Illumina [185344] 0 bladder diverticulum http://purl.obolibrary.org/obo/MONDO_0007197 GCST90084590 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M70: Soft tissue disorders related to use, overuse and pressure 5,010 European ancestry cases, 373,615 European ancestry controls NA Affymetrix, Illumina [502447] 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90080526 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.8: Other specified disorders of bladder (Gene-based burden) 7,761 European ancestry cases, 380,142 European ancestry controls NA Illumina [185344] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90084591 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R22: Localized swelling, mass and lump of skin and subcutaneous tissue 3,876 European ancestry cases, 374,735 European ancestry controls NA Affymetrix, Illumina [502404] 0 primary lymphedema http://purl.obolibrary.org/obo/MONDO_0019175 GCST90080823 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N32.9: Bladder disorder, unspecified (Gene-based burden) 964 European ancestry cases, 386,803 European ancestry controls NA Illumina [185344] 0 bladder disease http://www.ebi.ac.uk/efo/EFO_1000018 GCST90084592 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Calcium levels (UKB data field 30680) 378,246 European ancestry individuals 115,616 European ancestry individuals Affymetrix, Illumina [502369] 1 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90079023 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N35: Urethral stricture (Gene-based burden) 3,910 European ancestry cases, 383,819 European ancestry controls NA Illumina [185343] 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90084595 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. High density lipoprotein cholesterol levels (UKB data field 30760) 378,217 European ancestry individuals 93,238 European ancestry individuals Affymetrix, Illumina [502349] 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90079031 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N35.9: Urethral stricture, unspecified (Gene-based burden) 3,859 European ancestry cases, 383,951 European ancestry controls NA Illumina [185343] 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90084594 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E78.0: Pure hypercholesterolemia 45,730 European ancestry cases, 332,541 European ancestry controls 6,694 European ancestry cases, 75,390 European ancestry controls Affymetrix, Illumina [502240] 1 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90079766 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N36: Other disorders of urethra (Gene-based burden) 964 European ancestry cases, 386,607 European ancestry controls NA Illumina [185336] 0 urethral disease http://www.ebi.ac.uk/efo/EFO_0009689 GCST90084596 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L60: Nail disorders 3,890 European ancestry cases, 374,676 European ancestry controls NA Affymetrix, Illumina [502221] 0 nail anomaly http://purl.obolibrary.org/obo/MONDO_0019283 GCST90080357 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39: Other disorders of urinary system (Gene-based burden) 31,925 European ancestry cases, 337,879 European ancestry controls NA Illumina [185053] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90084602 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 G43: Migraine 8,426 European ancestry cases, 369,746 European ancestry controls NA Affymetrix, Illumina [502151] 0 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90079827 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.0: Urinary tract infection, site not specified (Gene-based burden) 19,361 European ancestry cases, 360,258 European ancestry controls NA Illumina [185202] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90084597 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Total protein levels (UKB data field 30860) 377,964 European ancestry individuals 107,967 European ancestry individuals Affymetrix, Illumina [502143] 1 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90079043 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.3: Stress incontinence (female) (male) (Gene-based burden) 6,784 European ancestry cases, 380,112 European ancestry controls NA Illumina [185333] 0 Stress urinary incontinence http://purl.obolibrary.org/obo/HP_0010992 GCST90084598 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. Glucose levels (UKB data field 30740) 377,948 European ancestry individuals 87,333 European ancestry individuals Affymetrix, Illumina [502130] 1 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90079029 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 N39.4: Other specified urinary incontinence (Gene-based burden) 2,037 European ancestry cases, 385,439 European ancestry controls NA Illumina [185343] 0 Urinary incontinence http://purl.obolibrary.org/obo/HP_0000020 GCST90084599 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 J90: Pleural effusion, not elsewhere classified (Gene-based burden) 7,231 European ancestry cases, 380,404 European ancestry controls NA Illumina [185342] 0 pleural effusion http://www.ebi.ac.uk/efo/EFO_0009637 GCST90084134 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 E05: Thyrotoxicosis [hyperthyroidism] 3,102 European ancestry cases, 383,241 European ancestry controls NA Affymetrix, Illumina [509296] 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90079730 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K02: Dental caries (Gene-based burden) 3,818 European ancestry cases, 383,967 European ancestry controls NA Illumina [185339] 0 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST90084151 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S00: Superficial injury of head 3,216 European ancestry cases, 383,001 European ancestry controls NA Affymetrix, Illumina [509182] 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90080941 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K02.9: Dental caries, unspecified (Gene-based burden) 3,669 European ancestry cases, 384,261 European ancestry controls NA Illumina [185344] 0 dental caries http://www.ebi.ac.uk/efo/EFO_0003819 GCST90084150 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K46: Unspecified abdominal hernia 730 European ancestry cases, 385,509 European ancestry controls NA Affymetrix, Illumina [509170] 0 Hernia of the abdominal wall http://purl.obolibrary.org/obo/HP_0004299 GCST90080229 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K04: Diseases of pulp and periapical tissues (Gene-based burden) 3,161 European ancestry cases, 381,325 European ancestry controls NA Illumina [185295] 0 dental pulp disease http://www.ebi.ac.uk/efo/EFO_0009540 GCST90084154 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 L03.9: Cellulitis and acute lymphangitis, unspecified 742 European ancestry cases, 385,471 European ancestry controls NA Affymetrix, Illumina [509167] 0 cellulitis, lymphangitis http://www.ebi.ac.uk/efo/EFO_0003035, http://www.ebi.ac.uk/efo/EFO_0007351 GCST90080330 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K04.5: Chronic apical periodontitis (Gene-based burden) 601 European ancestry cases, 387,329 European ancestry controls NA Illumina [185344] 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90084152 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M19.0: Primary osteoarthritis of other joints 1,787 European ancestry cases, 384,414 European ancestry controls NA Affymetrix, Illumina [509165] 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90080420 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K04.7: Periapical abscess without sinus (Gene-based burden) 1,228 European ancestry cases, 386,702 European ancestry controls NA Illumina [185344] 0 periapical tissue disease http://www.ebi.ac.uk/efo/EFO_0010688 GCST90084153 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 M22: Disorder of patella 1,228 European ancestry cases, 384,932 European ancestry controls NA Affymetrix, Illumina [509162] 0 disorder of patella http://www.ebi.ac.uk/efo/EFO_0009665 GCST90080433 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K05: Gingivitis and periodontal diseases (Gene-based burden) 1,081 European ancestry cases, 386,036 European ancestry controls NA Illumina [185327] 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90084156 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.3: Fracture of shaft of humerus 637 European ancestry cases, 385,560 European ancestry controls NA Affymetrix, Illumina [509152] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080979 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K05.3: Chronic periodontitis (Gene-based burden) 652 European ancestry cases, 387,269 European ancestry controls NA Illumina [185340] 0 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90084155 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 R19.5: Other fecal abnormalities 2,737 European ancestry cases, 383,417 European ancestry controls NA Affymetrix, Illumina [509137] 0 Abdominal symptom http://purl.obolibrary.org/obo/HP_0011458 GCST90080810 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K07: Dentofacial anomalies [including malocclusion] (Gene-based burden) 1,054 European ancestry cases, 384,162 European ancestry controls NA Illumina [185303] 0 Abnormality of the mouth http://purl.obolibrary.org/obo/HP_0000153 GCST90084157 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 S42.30: Unspecified fracture of shaft of humerus 575 European ancestry cases, 385,607 European ancestry controls NA Affymetrix, Illumina [509137] 0 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90080978 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K08: Other disorders of teeth and supporting structures (Gene-based burden) 3,287 European ancestry cases, 382,909 European ancestry controls NA Illumina [185319] 0 tooth disease http://www.ebi.ac.uk/efo/EFO_1001216 GCST90084160 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.1: Encounter for screening for diabetes mellitus 1,161 European ancestry cases, 384,967 European ancestry controls NA Affymetrix, Illumina [509129] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081214 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K08.3: Retained dental root (Gene-based burden) 1,946 European ancestry cases, 385,984 European ancestry controls NA Illumina [185344] 0 Abnormality of the dentition http://purl.obolibrary.org/obo/HP_0000164 GCST90084158 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z86.6: Personal history of diseases of the nervous system and sense organs 10,198 European ancestry cases, 376,004 European ancestry controls NA Affymetrix, Illumina [509128] 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90081362 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K08.8: Other specified disorders of teeth and supporting structures (Gene-based burden) 897 European ancestry cases, 387,033 European ancestry controls NA Illumina [185344] 0 Abnormality of the dentition http://purl.obolibrary.org/obo/HP_0000164 GCST90084159 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z92.8: Personal history of other medical treatment 722 European ancestry cases, 385,465 European ancestry controls NA Affymetrix, Illumina [509127] 0 clinical history http://www.ebi.ac.uk/efo/EFO_0000352 GCST90081410 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K09: Cysts of oral region, not elsewhere classified (Gene-based burden) 514 European ancestry cases, 387,207 European ancestry controls NA Illumina [185340] 0 Mediastinal Cyst http://www.ebi.ac.uk/efo/EFO_1001368 GCST90084161 Exome-wide sequencing 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 Z13.10: Encounter for screening for diabetes mellitus 902 European ancestry cases, 385,224 European ancestry controls NA Affymetrix, Illumina [509126] 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90081213 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2022-07-20 34662886 Backman JD 2021-10-18 Nature www.ncbi.nlm.nih.gov/pubmed/34662886 Exome sequencing and analysis of 454,787 UK Biobank participants. ICD10 K10: Other diseases of jaws (Gene-based burden) 537 European ancestry cases, 386,441 European ancestry controls NA Illumina [185332] 0 jaw disease http://www.ebi.ac.uk/efo/EFO_0009468 GCST90084162 Exome-wide sequencing 2019-04-24 30694715 Sakornsakolpat P 2019-01-29 Am J Respir Cell Mol Biol www.ncbi.nlm.nih.gov/pubmed/30694715 Genome-Wide Association Analysis of Single Breath Diffusing Capacity of Carbon Monoxide (DLCO). Diffusing capacity of carbon monoxide 2,584 European ancestry individuals with chronic obstructive pulmonary disease, 3,002 European ancestry healthy individuals, 343 African American individuals with chronic obstructive pulmonary disease, 1,006 African American healthy individuals NA Illumina [NR] (imputed) 55 diffusing capacity of the lung for carbon monoxide http://www.ebi.ac.uk/efo/EFO_0009369 GCST007637 Genome-wide genotyping array 2019-02-11 30697902 Hernandez-Pacheco N 2019-01-29 Clin Exp Allergy www.ncbi.nlm.nih.gov/pubmed/30697902 Genome-wide association study of inhaled corticosteroid response in admixed children with asthma. Asthma exacerbations in inhaled corticosteroid treatment 854 Hispanic/Latino cases, 493 African American cases 1,697 European ancestry cases Affymetrix [~ 8700000] (imputed) 16 asthma exacerbation measurement, response to corticosteroid http://www.ebi.ac.uk/efo/EFO_0007614, http://purl.obolibrary.org/obo/GO_0031960 GCST007100 Genome-wide genotyping array 2018-12-03 30343302 Kim SH 2018-10-19 Gynecol Obstet Invest www.ncbi.nlm.nih.gov/pubmed/30343302 High Genetic Risk Scores of ASIC2, MACROD2, CHRM3, and C2orf83 Genetic Variants Associated with Polycystic Ovary Syndrome Impair Insulin Sensitivity and Interact with Energy Intake in Korean Women. Polycystic ovary syndrome 182 Korean ancestry cases, 240 Korean ancestry controls NA Affymetrix [NR] 3 polycystic ovary syndrome http://www.ebi.ac.uk/efo/EFO_0000660 GCST006659 Genome-wide genotyping array 2018-07-19 29622589 Tereshchenko LG 2018-04-05 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/29622589 Genome-Wide Associations of Global Electrical Heterogeneity ECG Phenotype: The ARIC (Atherosclerosis Risk in Communities) Study and CHS (Cardiovascular Health Study). Global electrical heterogeneity phenotypes 3,057 Black individuals, 10,769 European ancestry individuals NA Affymetrix, Illumina [at least 9117794] (imputed) 15 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST005905 Genome-wide genotyping array 2018-07-11 29884306 Workalemahu T 2018-04-16 Placenta www.ncbi.nlm.nih.gov/pubmed/29884306 Genetic variations and risk of placental abruption: A genome-wide association study and meta-analysis of genome-wide association studies. Placental abruption 959 cases, 1553 controls NA Illumina [up to 4983952] (imputed) 9 Abruptio Placentae http://www.ebi.ac.uk/efo/EFO_1001754 GCST005844 Genome-wide genotyping array 2019-02-07 30692554 Bustos BI 2019-01-28 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30692554 Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry. Gallstone disease 529 Chilean Latino cases, 566 Chilean Latino controls 626 Chilean Latino cases, 1,017 Chilean Latino controls, 1,909 European ancestry cases, 4,183 European ancestry controls Affymetrix [9433911] (imputed) 2 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST007050 Genome-wide genotyping array 2018-06-11 29590334 Bjornsson T 2018-03-24 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/29590334 A rare missense mutation in MYH6 associates with non-syndromic coarctation of the aorta. Aortic coarctation 39 Icelandic ancestry cases, 140,661 Icelandic ancestry controls 81 Icelandic ancestry cases, 214,412 Icelandic ancestry controls Illumina [32500000] (imputed) 1 Aortic Coarctation http://www.ebi.ac.uk/efo/EFO_1001267 GCST005687 Genome-wide genotyping array 2018-05-29 29580174 Ala-Mutka EM 2018-03-27 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/29580174 Effect of hydrochlorothiazide on serum uric acid concentration: a genome-wide association study. Change in serum uric acid levels in response to thiazide diuretic treatment (hydrochlorothiazide) in hypertension 214 Finnish cases 465 Finnish cases Illumina [NR] (imputed) 0 response to hydrochlorothiazide, uric acid measurement http://www.ebi.ac.uk/efo/EFO_0005202, http://www.ebi.ac.uk/efo/EFO_0004761 GCST005646 Genome-wide genotyping array 2019-01-16 30361487 Yan Q 2018-10-25 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30361487 Genome-wide association study of brain amyloid deposition as measured by Pittsburgh Compound-B (PiB)-PET imaging. Cerebral amyloid deposition (PET imaging) 983 European ancestry individuals NR Illumina [at least 7000000] (imputed) 41 cerebral amyloid deposition measurement http://www.ebi.ac.uk/efo/EFO_0007707 GCST006904 Genome-wide genotyping array 2019-02-12 30369316 Low-Kam C 2018-08-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30369316 Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol. Cholesterol efflux capacity 3,487 French-Canadian ancestry cases, 1,806 French-Canadian ancestry controls NA Illumina [at least 9000000] (imputed) 4 cholesterol efflux capacity measurement http://www.ebi.ac.uk/efo/EFO_0009132 GCST007114 Genome-wide genotyping array 2019-02-12 30369316 Low-Kam C 2018-08-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30369316 Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol. Cholesterol efflux capacity (cAMP stimulated assay) 3,487 French-Canadian ancestry cases, 1,806 French-Canadian ancestry controls NA Illumina [at least 9000000] (imputed) 2 cholesterol efflux capacity measurement http://www.ebi.ac.uk/efo/EFO_0009132 GCST007115 Genome-wide genotyping array 2019-02-12 30369316 Low-Kam C 2018-08-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30369316 Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol. Cholesterol efflux capacity (ABCA-1 dependent assay) 3,487 French-Canadian ancestry cases, 1,806 French-Canadian ancestry controls NA Illumina [at least 9000000] (imputed) 3 cholesterol efflux capacity measurement http://www.ebi.ac.uk/efo/EFO_0009132 GCST007116 Genome-wide genotyping array 2019-02-12 30369316 Low-Kam C 2018-08-01 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/30369316 Variants at the APOE /C1/C2/C4 Locus Modulate Cholesterol Efflux Capacity Independently of High-Density Lipoprotein Cholesterol. Cholesterol efflux capacity (BHK stimulated assay) 3,487 French-Canadian ancestry cases, 1,806 French-Canadian ancestry controls NA Illumina [at least 9000000] (imputed) 1 cholesterol efflux capacity measurement http://www.ebi.ac.uk/efo/EFO_0009132 GCST007117 Genome-wide genotyping array 2019-07-16 29981864 Mohammadnejad A 2018-07-05 Ann Allergy Asthma Immunol www.ncbi.nlm.nih.gov/pubmed/29981864 A case-only genome-wide association study on gene-sex interaction in allergic rhinitis. Allergic rhinitis x sex interaction 184 Danish ancestry male cases, 250 Danish ancestry female cases NA Affymetrix [1348667] (imputed) 1 sex interaction measurement, allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0005854 GCST008138 Genome-wide genotyping array 2018-08-30 29875475 Montalvo-Ortiz JL 2018-06-06 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/29875475 Translational studies support a role for serotonin 2B receptor (HTR2B) gene in aggression-related cannabis response. Cannabis-related aggression 3,269 African American individuals, 2,546 European ancestry individuals 89 African American individuals Illumina [at least 8365931] (imputed) 0 aggressive behavior http://www.ebi.ac.uk/efo/EFO_0003015 GCST006175 Genome-wide genotyping array 2019-07-18 30988330 Hellwege JN 2019-04-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/30988330 Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE network. Benign prostatic hyperplasia 2,258 European ancestry cases, 398 African and unknown ancestry cases, 6,599 European ancestry controls, 1,164 African and unknown ancestry controls NA Affymetrix, Illumina [10973920] (imputed) 13 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST008169 Genome-wide genotyping array 2018-06-11 29594489 Apewokin S 2018-03-28 Support Care Cancer www.ncbi.nlm.nih.gov/pubmed/29594489 Host genetic susceptibility to Clostridium difficile infections in patients undergoing autologous stem cell transplantation: a genome-wide association study. Clostridium difficile infection in multiple myeloma 57 European ancestry cases, 589 European ancestry controls NA Illumina [892589] 59 clostridium difficile infection http://www.ebi.ac.uk/efo/EFO_0009130 GCST005686 Genome-wide genotyping array 2019-07-08 31006051 Kharazmi M 2019-04-20 Calcif Tissue Int www.ncbi.nlm.nih.gov/pubmed/31006051 A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture. Bisphosphonate-associated atypical femoral fracture 50 European ancestry cases, 1 Chilean ancestry case, 4,891 European ancestry controls NA Illumina [7585874] (imputed) 37 atypical femoral fracture, response to bisphosphonate http://www.ebi.ac.uk/efo/EFO_0009960, http://www.ebi.ac.uk/efo/EFO_0009958 GCST008097 Genome-wide genotyping array 2019-07-08 31006051 Kharazmi M 2019-04-20 Calcif Tissue Int www.ncbi.nlm.nih.gov/pubmed/31006051 A Genome-Wide Association Study of Bisphosphonate-Associated Atypical Femoral Fracture. Atypical femoral fracture in phosphonate treatment 50 European ancestry cases, 1 Chilean ancestry case, 324 European ancestry controls NA Illumina [7585874] (imputed) 14 atypical femoral fracture, response to bisphosphonate http://www.ebi.ac.uk/efo/EFO_0009960, http://www.ebi.ac.uk/efo/EFO_0009958 GCST008098 Genome-wide genotyping array 2019-07-26 31226226 Du Z 2019-06-21 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/31226226 A Genome-wide Association Study of Prostate Cancer in Latinos. Prostate cancer 2,714 Hispanic or Latin American cases, 5,239 Hispanic or Latin American controls NA Affymetrix, Illumina [10330976] (imputed) 3 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST008231 Genome-wide genotyping array 2019-06-21 31020675 Omae Y 2019-04-24 Transfusion www.ncbi.nlm.nih.gov/pubmed/31020675 Integrative genome analysis identified the KANNO blood group antigen as prion protein. KANNO antigen negativity 4 Japanese ancestry cases, 415 Japanese ancestry controls NA Affymetrix [642203] 1 KANNO antigen measurement http://www.ebi.ac.uk/efo/EFO_0009949 GCST007948 Genome-wide genotyping array 2019-07-18 31226389 Wilman HR 2019-06-18 J Hepatol www.ncbi.nlm.nih.gov/pubmed/31226389 Genetic studies of abdominal MRI data identify genes regulating hepcidin as major determinants of liver iron concentration. Liver iron content 8,289 European ancestry individuals 1,513 European ancestry individuals Affymetrix [NR] (imputed) 0 liver iron measurement http://www.ebi.ac.uk/efo/EFO_0010056 GCST008172 Genome-wide genotyping array 2018-06-29 28584286 Warrier V 2017-06-06 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/28584286 Genome-wide meta-analysis of cognitive empathy: heritability, and correlates with sex, neuropsychiatric conditions and cognition. Cognitive empathy 45,465 European ancestry females, 44,088 European ancestry males NA Illumina [11133794] (imputed) 125 empathy measurement http://www.ebi.ac.uk/efo/EFO_0009183 GCST005755 Genome-wide genotyping array 2020-02-11 31835028 Cross-Disorder Group of the Psychiatric Genomics Consortium 2019-12-01 Cell www.ncbi.nlm.nih.gov/pubmed/31835028 Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders. Anorexia nervosa, attention-deficit/hyperactivity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, or Tourette syndrome (pleiotropy) 19,009 European ancestry ADHD cases, 3,495 European ancestry anorexia cases, 18,381 European ancestry autism cases, 20,352 European ancestry bipolar disorder cases, 130,664 European ancestry major depression cases, 2,688 European ancestry OCD cases, 33,640 European ancestry schizophrenia cases, 4,645 European ancestry Tourette's cases, 494,162 European ancestry controls NA NR [6786993] (imputed) 146 obsessive-compulsive disorder, attention deficit hyperactivity disorder, Tourette syndrome, unipolar depression, bipolar disorder, autism spectrum disorder, schizophrenia, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0004242, http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0004895, http://www.ebi.ac.uk/efo/EFO_0003761, http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003756, http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005351 GCST009600 Genome-wide genotyping array 2019-07-19 31219225 Young KA 2019-06-20 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/31219225 Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium. Alanine aminotransferase levels 3,595 Mexican American ancestry individuals NA Illumina [659211] 9 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST008173 Genome-wide genotyping array 2019-07-19 31219225 Young KA 2019-06-20 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/31219225 Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium. Gamma glutamyl transferase levels 1,577 Mexican American ancestry individuals NA Illumina [655023] 8 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST008175 Genome-wide genotyping array 2019-07-19 31219225 Young KA 2019-06-20 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/31219225 Genome-Wide Association Study Identifies Loci for Liver Enzyme Concentrations in Mexican Americans: The GUARDIAN Consortium. Aspartate aminotransferase levels 3,644 Mexican American ancestry individuals NA Illumina [659222] 6 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST008174 Genome-wide genotyping array 2019-05-07 30910378 Zanetti D 2019-03-12 Kidney Int www.ncbi.nlm.nih.gov/pubmed/30910378 Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion. Urinary albumin-to-creatinine ratio 218,759 European ancestry individuals 109,530 European ancestry individuals Affymetrix [19420026] (imputed) 12 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST007718 Genome-wide genotyping array 2019-05-07 30910378 Zanetti D 2019-03-12 Kidney Int www.ncbi.nlm.nih.gov/pubmed/30910378 Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion. Urinary potassium to creatinine ratio 218,435 European ancestry individuals 109,178 European ancestry individuals Affymetrix [19420026] (imputed) 4 urinary potassium to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0009882 GCST007721 Genome-wide genotyping array 2019-05-10 30910378 Zanetti D 2019-03-12 Kidney Int www.ncbi.nlm.nih.gov/pubmed/30910378 Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion. Urinary sodium to creatinine ratio 218,450 European ancestry individuals 109,166 European ancestry individuals Affymetrix [19420026] (imputed) 2 urinary sodium to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0009883 GCST007778 Genome-wide genotyping array 2019-05-07 30910378 Zanetti D 2019-03-12 Kidney Int www.ncbi.nlm.nih.gov/pubmed/30910378 Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion. Urinary sodium to potassium ratio 217,996 European ancestry individuals 108,942 European ancestry individuals Affymetrix [19420026] (imputed) 1 urinary sodium to potassium ratio http://www.ebi.ac.uk/efo/EFO_0009884 GCST007717 Genome-wide genotyping array 2019-05-07 30910378 Zanetti D 2019-03-12 Kidney Int www.ncbi.nlm.nih.gov/pubmed/30910378 Identification of 22 novel loci associated with urinary biomarkers of albumin, sodium, and potassium excretion. Albuminuria 217,634 European ancestry individuals 108,800 European ancestry individuals Affymetrix [19420026] (imputed) 8 albuminuria http://www.ebi.ac.uk/efo/EFO_0004285 GCST007719 Genome-wide genotyping array 2018-06-22 29603866 Pain O 2018-03-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/29603866 Genome-wide analysis of adolescent psychotic-like experiences shows genetic overlap with psychiatric disorders. Anhedonia 4,937 European ancestry individuals, 821 European ancestry sibling pairs 1,089 European ancestry individuals, 635 European ancestry monozygotic twin pairs Affymetrix, Illumina [4487870] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST005718 Genome-wide genotyping array 2018-06-22 29603866 Pain O 2018-03-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/29603866 Genome-wide analysis of adolescent psychotic-like experiences shows genetic overlap with psychiatric disorders. Cognitive disorganisation 1,981 European ancestry individuals, 2,158 European ancestry sibling pairs NA Affymetrix, Illumina [4487870] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST005719 Genome-wide genotyping array 2018-06-22 29603866 Pain O 2018-03-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/29603866 Genome-wide analysis of adolescent psychotic-like experiences shows genetic overlap with psychiatric disorders. Parent-rated negative symptoms 5,642 European ancestry individuals, 2,228 European ancestry sibling pairs NA Affymetrix, Illumina [4487870] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST005720 Genome-wide genotyping array 2018-06-22 29603866 Pain O 2018-03-31 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/29603866 Genome-wide analysis of adolescent psychotic-like experiences shows genetic overlap with psychiatric disorders. Paranoia and hallucinations 5,313 European ancestry individuals, 1,676 European ancestry sibling pairs NA Affymetrix, Illumina [4487870] (imputed) 0 psychotic symptom measurement http://www.ebi.ac.uk/efo/EFO_0009182 GCST005717 Genome-wide genotyping array 2019-06-20 29124443 Yasukochi Y 2017-11-09 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/29124443 Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. Chronic kidney disease 606 Japanese ancestry cases, 1,040 Japanese ancestry controls 2,517 Japanese ancestry cases, 885 Japanese ancestry controls Illumina [~ 244000] 16 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST007920 Exome genotyping array [Exome array] 2019-06-20 29124443 Yasukochi Y 2017-11-09 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/29124443 Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. Hyperuricemia 847 Japanese ancestry cases, 4,640 Japanese ancestry controls 972 Japanese ancestry cases, 4,584 Japanese ancestry controls Illumina [~ 244000] 23 hyperuricemia http://www.ebi.ac.uk/efo/EFO_0009104 GCST007916 Exome genotyping array [Exome array] 2019-06-20 29124443 Yasukochi Y 2017-11-09 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/29124443 Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. Serum uric acid levels 5,847 Japanese ancestry individuals NA Illumina [~ 244000] 28 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST007918 Exome genotyping array [Exome array] 2019-06-20 29124443 Yasukochi Y 2017-11-09 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/29124443 Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. Estimated glomerular filtration rate 5,636 Japanese ancestry individuals NA Illumina [~ 244000] 20 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST007917 Exome genotyping array [Exome array] 2019-06-20 29124443 Yasukochi Y 2017-11-09 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/29124443 Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. Creatinine levels 5,636 Japanese ancestry individuals NA Illumina [~ 244000] 21 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST007919 Exome genotyping array [Exome array] 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety and stress-related disorders 12,655 European ancestry cases, 19,225 European ancestry controls NA Illumina [8933939] (imputed) 10 anxiety disorder, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0010098 GCST008559 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Stress-related disorders 9,831 European ancestry cases, 19,225 European ancestry controls NA Illumina [8933939] (imputed) 1 stress-related disorder http://www.ebi.ac.uk/efo/EFO_0010098 GCST008567 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety disorders 4,584 European ancestry cases, 19,225 European ancestry controls NA Illumina [8933939] (imputed) 1 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST008566 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety and stress-related disorders (excluding adjustment disorder) 8,517 European ancestry cases, 19,225 European ancestry controls NA Illumina [8933939] (imputed) 1 anxiety disorder, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0010098 GCST008565 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety and stress-related disorders (excluding co-morbid schizophrenia) 11,560 European ancestry cases, 19,225 European ancestry controls NA Illumina [8933939] (imputed) 1 anxiety disorder, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0010098 GCST008564 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety and stress-related disorders (including obsessive-compulsive disorder) 13,533 European ancestry cases, 19,225 European ancestry controls NA Illumina [8933939] (imputed) 1 anxiety disorder, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0010098 GCST008563 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety and stress-related disorders (psychiatric co-morbidity weighting design) 10,311 European ancestry cases, 19,225 European ancestry controls NA Illumina [8933939] (imputed) 1 anxiety disorder, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0010098 GCST008562 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety and stress-related disorders (psychiatric co-morbidity covariate model) 12,096 European ancestry cases, 42,215 European ancestry controls NA Illumina [8933939] (imputed) 1 anxiety disorder, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0010098 GCST008561 Genome-wide genotyping array 2019-09-02 31116379 Meier SM 2019-05-22 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/31116379 Genetic Variants Associated With Anxiety and Stress-Related Disorders: A Genome-Wide Association Study and Mouse-Model Study. Anxiety and stress-related disorders (propensity-score-matching design) 11,599 European ancestry cases, 11,599 European ancestry controls NA Illumina [8933939] (imputed) 0 anxiety disorder, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0010098 GCST008560 Genome-wide genotyping array 2019-03-26 28714469 Langefeld CD 2017-07-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28714469 Transancestral mapping and genetic load in systemic lupus erythematosus. Systemic lupus erythematosus 6,748 European ancestry cases, 11,516 European ancestry controls NA Illumina [at least 5000000] (imputed) 71 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST007400 Targeted genotyping array [ImmunoChip] 2018-06-29 28714469 Langefeld CD 2017-07-17 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28714469 Transancestral mapping and genetic load in systemic lupus erythematosus. Systemic lupus erythematosus 6,748 European ancestry cases, 11,516 European ancestry controls, 2,970 African American cases, 2,452 African American controls, 1,872 Hispanic cases, 2,016 Hispanic controls NA Illumina [at least 5000000] (imputed) 183 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST005752 Targeted genotyping array [ImmunoChip] 2018-06-21 29628937 Jiang J 2018-03-23 Front Genet www.ncbi.nlm.nih.gov/pubmed/29628937 A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood. Growth differentiation factor-15 levels (conditioned on rs888663) 4,633 European ancestry individuals 807 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 2 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST005712 Genome-wide genotyping array 2018-06-21 29628937 Jiang J 2018-03-23 Front Genet www.ncbi.nlm.nih.gov/pubmed/29628937 A Meta-Analysis of Genome-Wide Association Studies of Growth Differentiation Factor-15 Concentration in Blood. Growth differentiation factor-15 levels 4,633 European ancestry individuals 807 European ancestry individuals Affymetrix, Illumina [~ 2500000] (imputed) 1 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST005711 Genome-wide genotyping array 2018-05-01 29581620 Fujii R 2018-02-01 Nagoya J Med Sci www.ncbi.nlm.nih.gov/pubmed/29581620 Genome-wide association study for pollinosis identified two novel loci in interleukin (IL)-1B in a Japanese population. Pollinosis 731 Japanese ancestry individuals 560 Japanese ancestry individuals Illumina [570398] 0 seasonal allergic rhinitis http://www.ebi.ac.uk/efo/EFO_0003956 GCST005556 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Soluble E-selectin levels 5,284 Finnish ancestry individuals NA Illumina [NR] (imputed) 2 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST008202 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Soluble ICAM-1 5,284 Finnish ancestry individuals NA Illumina [NR] (imputed) 3 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST008210 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Soluble VCAM-1 levels 5,284 Finnish ancestry individuals NA Illumina [NR] (imputed) 3 vascular cell adhesion molecule-1 measurement http://www.ebi.ac.uk/efo/EFO_0010057 GCST008196 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interleukin-1-alpha levels 5,284 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST008207 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Soluble CD40 ligand levels 5,284 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST008208 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Plasminogen activator inhibitor-1 (PAI-1) levels 5,284 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST008206 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Vascular endothelial growth factor levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 3 vascular endothelial growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004762 GCST008198 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interleukin-17 levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 interleukin 17 measurement http://www.ebi.ac.uk/efo/EFO_0008174 GCST008205 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Monocyte chemoattractant protein-1 levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 1 CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004749 GCST008204 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interleukin-1-beta levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 2 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST008209 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interleukin-1-receptor antagonist levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST008203 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interleukin-4 levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 interleukin 4 measurement http://www.ebi.ac.uk/efo/EFO_0008184 GCST008201 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interleukin-6 levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST008200 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interleukin-8 levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 0 interleukin 8 measurement http://www.ebi.ac.uk/efo/EFO_0008191 GCST008197 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Interferon gamma-induced protein 10 levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 1 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST008199 Genome-wide genotyping array 2019-07-22 31217265 Sliz E 2019-06-19 J Med Genet www.ncbi.nlm.nih.gov/pubmed/31217265 Genome-wide association study identifies seven novel loci associating with circulating cytokines and cell adhesion molecules in Finns. Tumor necrosis factor alpha levels 13,577 Finnish ancestry individuals NA Illumina [NR] (imputed) 1 tumor necrosis factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0004684 GCST008211 Genome-wide genotyping array 2018-09-20 29626450 Bonfiglio F 2018-04-04 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/29626450 Female-specific Association Between Variants on Chromosome 9 and Self-reported Diagnosis of Irritable Bowel Syndrome. Irritable bowel syndrome 7,130 British ancestry women cases, 2,446 British ancestry men cases, 178,076 British ancestry women controls, 158,423 British ancestry men controls NA Affymetrix [7287191] (imputed) 15 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST006304 Genome-wide genotyping array 2019-05-28 25625282 Mahajan A 2015-01-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25625282 Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. Fasting blood insulin adjusted for BMI up to 30,825 non-diabetic individuals NA Illumina [106489] 6 BMI-adjusted fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0008037 GCST007857 Targeted genotyping array [Exome array] 2019-05-28 25625282 Mahajan A 2015-01-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25625282 Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. Fasting blood glucose adjusted for BMI up to 33,231 non-diabetic individuals NA Illumina [106489] 10 BMI-adjusted fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0008036 GCST007858 Targeted genotyping array [Exome array] 2018-07-19 29621232 Spracklen CN 2018-04-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29621232 Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey. Fasting blood glucose 5,786 Chinese ancestry individuals NA Illumina [8045193] (imputed) 5 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST005913 Genome-wide genotyping array 2018-07-19 29621232 Spracklen CN 2018-04-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29621232 Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey. Fasting blood insulin 5,786 Chinese ancestry individuals NA Illumina [8045193] (imputed) 1 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST005915 Genome-wide genotyping array 2018-07-19 29621232 Spracklen CN 2018-04-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29621232 Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey. Glycated hemoglobin levels 6,943 Chinese ancestry individuals NA Illumina [8045193] (imputed) 1 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST005914 Genome-wide genotyping array 2018-07-19 29621232 Spracklen CN 2018-04-05 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/29621232 Identification and functional analysis of glycemic trait loci in the China Health and Nutrition Survey. Type 2 diabetes 748 Chinese ancestry cases, 4,983 Chinese ancestry controls NA Illumina [8045193] (imputed) 3 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST005912 Genome-wide genotyping array 2018-07-20 29618737 Napier MD 2018-04-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29618737 Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy. Ventricular ectopy or supraventricular ectopy (pleiotropy) 1,618 European ancestry supraventricular ectopy cases, 652 African ancestry supraventricular ectopy cases, 354 Hispanic/Latino ancestry supraventricular ectopy cases, 2,468 European ancestry ventricular ectopy cases, 481 African ancestry ventricular ectopy cases, 168 Hispanic/Latino ancestry ventricular ectopy cases, at least 19,586 European ancestry controls, at least 8,141 African ancestry controls, at least 10,663 Hispanic/Latino ancestry controls. NA Affymetrix, Illumina [NR] (imputed) 2 premature cardiac contractions, supraventricular ectopy, ventricular ectopy http://www.ebi.ac.uk/efo/EFO_0009275, http://www.ebi.ac.uk/efo/EFO_0009277, http://www.ebi.ac.uk/efo/EFO_0009276 GCST005935 Genome-wide genotyping array 2018-07-20 29618737 Napier MD 2018-04-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29618737 Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy. Ventricular ectopy 2,468 European ancestry cases, 21,204 European ancestry controls, 481 African ancestry cases, 8,793 African ancestry controls, 168 Hispanic/Latino ancestry cases, 11,017 Hispanic/Latino ancestry controls NA Affymetrix, Illumina [NR] (imputed) 4 ventricular ectopy http://www.ebi.ac.uk/efo/EFO_0009276 GCST005937 Genome-wide genotyping array 2018-07-20 29618737 Napier MD 2018-04-04 Sci Rep www.ncbi.nlm.nih.gov/pubmed/29618737 Genome-wide association study and meta-analysis identify loci associated with ventricular and supraventricular ectopy. Supraventricular ectopy 1,618 European ancestry cases, 20,899 European ancestry controls, 652 African ancestry cases, 8,622 African ancestry controls, 354 Hispanic/Latino ancestry cases, 10,831 Hispanic/Latino ancestry controls NA Affymetrix, Illumina [NR] (imputed) 6 supraventricular ectopy http://www.ebi.ac.uk/efo/EFO_0009277 GCST005936 Genome-wide genotyping array 2019-10-23 30902966 Mufford M 2019-03-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30902966 Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Tourette syndrome or brain region volumes (pleiotropy) 4,644 European ancestry Tourette syndrome cases, 8,695 European ancestry Tourette syndrome controls, 30,717 European ancestry individuals with subcortical brain volume measurements NA NR [7682991] 0 Tourette syndrome, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0004895, http://www.ebi.ac.uk/efo/EFO_0006930 GCST008907 Genome-wide genotyping array 2019-10-23 30902966 Mufford M 2019-03-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30902966 Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Social disinhibition in Tourette syndrome or subcortical volume measurements (pleiotropy) 1,414 European ancestry Tourette syndrome cases with social disinhibition measurements, 30,717 European ancestry individuals with subcortical brain volume measurements NA NR [7682991] 0 behavioural disinhibition measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006946, http://www.ebi.ac.uk/efo/EFO_0006930 GCST008908 Genome-wide genotyping array 2019-10-23 30902966 Mufford M 2019-03-22 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/30902966 Concordance of genetic variation that increases risk for tourette syndrome and that influences its underlying neurocircuitry. Symmetry behaviour in Tourette syndrome or subcortical volume measurements (pleiotropy) 1,419 European ancestry Tourette syndrome cases with symmetry behaviour measurements, 30,717 European ancestry individuals with subcortical brain volume measurements NA NR [7682991] (imputed) 0 obsessive-compulsive symptom measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0007802, http://www.ebi.ac.uk/efo/EFO_0006930 GCST008909 Genome-wide genotyping array 2018-07-10 29559929 Amare AT 2018-03-06 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/29559929 Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder. Response to SSRI in MDD or conscientiousness 865 individuals with SSRI response data, 260,861 individuals with personality trait data NA NR [NR] (imputed) 1 conscientiousness measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0007912, http://www.ebi.ac.uk/efo/EFO_0005658 GCST005836 Genome-wide genotyping array 2018-07-10 29559929 Amare AT 2018-03-06 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/29559929 Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder. Remission after SSRI treatment in MDD or neuroticism 865 individuals with SSRI response data, 170,911 individuals with personality trait data NA NR [NR] (imputed) 7 neuroticism measurement, response to selective serotonin reuptake inhibitor http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0005658 GCST005835 Genome-wide genotyping array 2018-07-10 29559929 Amare AT 2018-03-06 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/29559929 Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder. Remission after SSRI treatment in MDD or openness 865 individuals with SSRI response data, 260,861 individuals with personality trait data NA NR [NR] (imputed) 6 response to selective serotonin reuptake inhibitor, openness measurement http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0007914 GCST005833 Genome-wide genotyping array 2018-07-10 29559929 Amare AT 2018-03-06 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/29559929 Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder. Response to SSRI in MDD or openness 865 individuals with SSRI response data, 260,861 individuals with personality trait data NA NR [NR] (imputed) 6 response to selective serotonin reuptake inhibitor, openness measurement http://www.ebi.ac.uk/efo/EFO_0005658, http://www.ebi.ac.uk/efo/EFO_0007914 GCST005834 Genome-wide genotyping array 2018-05-18 29625478 Papakostas TD 2018-03-01 Invest Ophthalmol Vis Sci www.ncbi.nlm.nih.gov/pubmed/29625478 Genetic Risk Factors for Radiation Vasculopathy. Vision loss in proton beam irradiation treatment of choroidal melanoma 50 treated cases, 76 treated controls NA Illumina [1569667] 0 response to radiation, visual acuity measurement http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0008385 GCST005589 Genome-wide genotyping array 2019-02-13 30357299 De T 2018-10-01 JAMA www.ncbi.nlm.nih.gov/pubmed/30357299 Association of Genetic Variants With Warfarin-Associated Bleeding Among Patients of African Descent. Warfarin-associated bleeding 31 African American cases, 184 African American controls 40 African American cases, 148 African American controls Illumina [8152232] (imputed) 1 response to anticoagulant http://purl.obolibrary.org/obo/GO_0061476 GCST007137 Genome-wide genotyping array 2019-05-02 30921371 Choi SY 2019-03-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/30921371 Genome-wide association study of coronary artery calcification in asymptomatic Korean populations. Severe coronary artery calcification 100 Korean ancestry cases, 300 Korean ancestry controls 227 Korean ancestry cases, 1,061 Korean ancestry controls Affymetrix [550779] 0 coronary artery calcification http://www.ebi.ac.uk/efo/EFO_0004723 GCST007711 Genome-wide genotyping array 2019-05-10 30699873 van der Merwe C 2018-11-13 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/30699873 Concordance of genetic variation that increases risk for anxiety disorders and posttraumatic stress disorders and that influences their underlying neurocircuitry. Anxiety disorder or brain volume (pleiotropy) 7,016 European ancestry anxiety disorder cases, 14,745 European ancestry controls, 13,171 European ancestry individuals NA NR [up to 5661273] (imputed) 0 anxiety disorder, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006788, http://www.ebi.ac.uk/efo/EFO_0006930 GCST007775 Genome-wide genotyping array 2019-05-10 30699873 van der Merwe C 2018-11-13 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/30699873 Concordance of genetic variation that increases risk for anxiety disorders and posttraumatic stress disorders and that influences their underlying neurocircuitry. Post-traumatic stress disorder or brain volume (pleiotropy) 2,424 European ancestry post-traumatic stress disorder cases, 7,113 European ancestry controls, 13,171 European ancestry individuals NA NR [8156675] (imputed) 0 post-traumatic stress disorder, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0001358, http://www.ebi.ac.uk/efo/EFO_0006930 GCST007776 Genome-wide genotyping array 2019-05-15 30737484 Thomsen H 2019-02-08 Leukemia www.ncbi.nlm.nih.gov/pubmed/30737484 Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma. Monoclonal gammopathy of undetermined significance 992 European ancestry cases, 2,910 European ancestry controls NA Illumina [10258281] (imputed) 10 monoclonal gammopathy http://www.ebi.ac.uk/efo/EFO_0000203 GCST007824 Genome-wide genotyping array 2019-02-21 30504769 Ferkingstad E 2018-11-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30504769 Genome-wide association meta-analysis yields 20 loci associated with gallstone disease. Gallstone disease 27,174 European ancestry cases, 736,838 European ancestry controls NA Affymetrix, Illumina [43000000] (imputed) 28 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST007209 Genome-wide genotyping array 2019-03-10 30510082 Qian M 2018-12-03 Blood www.ncbi.nlm.nih.gov/pubmed/30510082 Novel susceptibility variants at the ERG locus for childhood acute lymphoblastic leukemia in Hispanics. Acute lymphoblastic leukemia (B-cell precursor) 940 Hispanic children cases, 681 Hispanic controls 144 Hispanic cases, 441 Hispanic controls, 2,317 European ancestry cases, 2,050 European ancestry controls, 227 African American cases, 1,380 African American controls Affymetrix [572556] (imputed) 0 acute lymphoblastic leukemia http://www.ebi.ac.uk/efo/EFO_0000220 GCST007276 Genome-wide genotyping array 2018-11-16 29857070 Gao J 2018-05-29 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/29857070 Association study and fine-mapping major histocompatibility complex analysis of pemphigus vulgaris in a Han Chinese population. Pemphigus vulgaris 240 Han Chinese ancestry cases, 1,031 Han Chinese ancestry controls 252 Han Chinese ancestry cases, 1,852 Han Chinese ancestry controls Illumina [802980] 5 pemphigus vulgaris http://www.ebi.ac.uk/efo/EFO_0004719 GCST006584 Genome-wide genotyping array 2019-06-20 31089239 Choe EK 2019-05-14 Sci Rep www.ncbi.nlm.nih.gov/pubmed/31089239 Genome-wide association study of right-sided colonic diverticulosis in a Korean population. Right-sided colonic diverticulosis 893 Korean ancestry cases, 1,075 Korean ancestry controls 346 Korean ancestry cases, 305 Korean ancestry controls Affymetrix [up to 755820] 2 Colonic diverticula http://purl.obolibrary.org/obo/HP_0002253 GCST007921 Genome-wide genotyping array 2019-05-22 31070453 Zekavat SM 2019-04-11 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31070453 Genetic Association of Finger Photoplethysmography-Derived Arterial Stiffness Index With Blood Pressure and Coronary Artery Disease. Arterial stiffness 131,686 British ancestry individuals NA Affymetrix [13995214] (imputed) 6 arterial stiffness measurement http://www.ebi.ac.uk/efo/EFO_0004517 GCST007846 Genome-wide genotyping array 2019-05-02 30511388 Yan W 2018-12-03 Clin Genet www.ncbi.nlm.nih.gov/pubmed/30511388 A genome-wide association study identifies new genes associated with developmental dysplasia of the hip. Developmental dysplasia of the hip 386 Han Chinese ancestry cases, 500 Han Chinese ancestry controls 574 Han Chinese ancestry cases, 569 Han Chinese ancestry controls Illumina [689141] 0 developmental dysplasia of the hip http://www.ebi.ac.uk/efo/EFO_1000648 GCST007699 Genome-wide genotyping array 2019-07-29 31070471 Akinkuolie AO 2019-04-11 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/31070471 Group IIA Secretory Phospholipase A2 and Incident Cardiovascular Disease. Group IIA secretory phospholipase A2 levels in individuals with elevated hsCRP 6,692 European ancestry individuals NA Illumina [796141] 14 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST008260 Genome-wide genotyping array 2019-08-13 31250797 Brick LA 2019-05-01 J Stud Alcohol Drugs www.ncbi.nlm.nih.gov/pubmed/31250797 Characterization of DSM-IV Opioid Dependence Among Individuals of European Ancestry. Opioid dependence 2,120 European ancestry cases, 1,944 European ancestry controls NA Illumina [6200495] (imputed) 7 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST008424 Genome-wide genotyping array 2019-06-28 31113495 Evans KL 2019-05-21 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/31113495 Genetics of heart rate in heart failure patients (GenHRate). Heart rate in heart failure with reduced ejection fraction 523 European ancestry individuals, 520 African American individuals NA Affymetrix [at least 600000] (imputed) 170 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST007999 Genome-wide genotyping array 2019-05-15 28272467 Heilmann-Heimbach S 2017-03-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/28272467 Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness. Male-pattern baldness 10,846 European ancestry cases, 11,672 European ancestry controls NA Affymetrix, Illumina [8004650] (imputed) 63 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST007815 Genome-wide genotyping array, Targeted genotyping array 2019-08-28 31250787 Fawns-Ritchie C 2019-06-01 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/31250787 Genetic Contributions to Health Literacy. Health literacy 1,771 English ancestry cases, 4,012 English ancestry controls NA Illumina [NR] (imputed) 38 health literacy measurement http://www.ebi.ac.uk/efo/EFO_0010104 GCST008513 Genome-wide genotyping array 2019-08-13 31249589 Edwards TL 2019-06-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/31249589 A Trans-Ethnic Genome-Wide Association Study of Uterine Fibroids. Uterine fibroids 8,168 European ancestry cases, 65,134 European ancestry controls, 1,278 African ancestry cases, 1,914 African ancestry controls 12,111 European ancestry cases, 138,477 European ancestry controls, 247 African ancestry cases, 713 African ancestry controls Affymetrix, Illumina [NR] (imputed) 11 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST008423 Genome-wide genotyping array 2019-08-13 31251759 Swenson BR 2019-06-28 PLoS One www.ncbi.nlm.nih.gov/pubmed/31251759 GWAS of QRS duration identifies new loci specific to Hispanic/Latino populations. QRS duration 15,124 Hispanic or Latin American individuals NA Affymetrix, Illumina [~ 21000000] (imputed) 10 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST008422 Genome-wide genotyping array 2019-03-28 30510157 Franceschini N 2018-12-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30510157 GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes. Carotid intima media thickness Up to 71,128 European ancestry individuals NA Affymetrix, Illumina [9574088] (imputed) 13 common carotid intimal medial thickness http://www.ebi.ac.uk/efo/EFO_0004860 GCST007436 Genome-wide genotyping array 2019-03-28 30510157 Franceschini N 2018-12-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30510157 GWAS and colocalization analyses implicate carotid intima-media thickness and carotid plaque loci in cardiovascular outcomes. Carotid plaque Up to 21,540 European ancestry cases, up to 26,894 European ancestry controls NA Affymetrix, Illumina [8578107] (imputed) 7 carotid atherosclerosis http://www.ebi.ac.uk/efo/EFO_0009783 GCST007435 Genome-wide genotyping array 2020-04-22 30206226 Chang J 2018-09-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/30206226 Exome-wide analysis identifies three low-frequency missense variants associated with pancreatic cancer risk in Chinese populations. Pancreatic cancer 943 Chinese ancestry cases, 3,908 Chinese ancestry controls 2,142 Chinese ancestry cases, 4,697 Chinese ancestry controls Illumina [174391] 3 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST009895 Exome genotyping array [Exome array] 2019-03-18 30514930 Mukherjee S 2018-12-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30514930 Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Alzheimer's disease with memory domain impairment Up to 1,107 European ancestry cases, 3,447 European ancestry controls NA NR [up to 6398204] (imputed) 2 Alzheimer disease, memory impairment http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0001072 GCST007330 Genome-wide genotyping array 2019-03-18 30514930 Mukherjee S 2018-12-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30514930 Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Alzheimer's disease with language domain impairment Up to 510 European ancestry cases, 3,447 European ancestry controls NA NR [up to 6398204] (imputed) 6 Alzheimer disease, language impairment http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0005425 GCST007334 Genome-wide genotyping array 2019-03-17 30514930 Mukherjee S 2018-12-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30514930 Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Alzheimer's disease with visuospatial domain impairment Up to 497 European ancestry cases, 3,447 European ancestry controls NA NR [up to 6398204] (imputed) 9 Alzheimer disease, visuospatial impairment http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0009752 GCST007318 Genome-wide genotyping array 2019-03-18 30514930 Mukherjee S 2018-12-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30514930 Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Alzheimer's disease with multiple cognitive domain impairments Up to 248 European ancestry cases, 3,447 European ancestry controls NA NR [up to 6398204] (imputed) 9 Alzheimer disease, Cognitive impairment http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/HP_0100543 GCST007332 Genome-wide genotyping array 2019-03-18 30514930 Mukherjee S 2018-12-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30514930 Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Alzheimer's disease with no specific cognitive domain impairment Up to 1,584 European ancestry cases, 3,447 European ancestry controls NA NR [up to 6398204] (imputed) 7 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST007333 Genome-wide genotyping array 2019-03-18 30514930 Mukherjee S 2018-12-04 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/30514930 Genetic data and cognitively defined late-onset Alzheimer's disease subgroups. Alzheimer's disease 2,431 European ancestry cases, 3,447 European ancestry controls NA NR [up to 6398204] (imputed) 0 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST007331 Genome-wide genotyping array 2018-07-09 29848360 Julia A 2018-05-30 Arthritis Res Ther www.ncbi.nlm.nih.gov/pubmed/29848360 Genome-wide association study meta-analysis identifies five new loci for systemic lupus erythematosus. Systemic lupus erythematosus 4,943 European ancestry cases, 8,483 European ancestry controls NA Illumina [7110321] (imputed) 5 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST005831 Genome-wide genotyping array 2019-07-11 31241743 Jaeger M 2019-04-24 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/31241743 A Genome-Wide Functional Genomics Approach Identifies Susceptibility Pathways to Fungal Bloodstream Infection in Humans. Candidemia 161 European ancestry cases, 152 European ancestry controls NA Illumina [5326313] (imputed) 8 Candidemia http://www.ebi.ac.uk/efo/EFO_1001282 GCST008106 Genome-wide genotyping array 2019-08-01 31058715 St Jean PL 2019-05-01 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/31058715 Pharmacogenetic analysis of belimumab fails to identify robust genetic predictors of efficacy in lupus. Response to belimumab (SLE response index) in systemic lupus erythematosus 443 European, Asian, American Indian or Alaskan Native, African American or unknown ancestry responders, 373 European, Asian, American Indian or Alaskan Native, African American or unknown ancestry non-responders 101 Northeast Asian ancestry responders, 103 Northeast Asian ancestry non-responders Affymetrix, Illumina [10900000] (imputed) 0 response to belimumab http://www.ebi.ac.uk/efo/EFO_0010077 GCST008307 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein disulfide-isomerase A4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248918 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein disulfide-isomerase A5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein disulfide-isomerase A5 measurement http://www.ebi.ac.uk/efo/EFO_0801941 GCST90248919 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein disulfide-isomerase A6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248920 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein DJ-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein dj-1 measurement http://www.ebi.ac.uk/efo/EFO_0020670 GCST90248921 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248922 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248923 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolow-density lipoprotein receptor-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 prolow-density lipoprotein receptor-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801929 GCST90248924 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Dos levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248925 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-phosphoinositide-dependent protein kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 3-phosphoinositide-dependent protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020116 GCST90248926 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyruvate dehydrogenase protein X component, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248927 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Putative D-tyrosyl-tRNA(Tyr) deacylase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248928 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyridoxal kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 pyridoxal kinase measurement http://www.ebi.ac.uk/efo/EFO_0021919 GCST90248929 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PDZ domain-containing protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 PDZ domain-containing protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0802850 GCST90248930 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PDZ domain-containing protein GIPC1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248931 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PDZ and LIM domain protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248932 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PDZ and LIM domain protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 PDZ and LIM domain protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802849 GCST90248933 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein eva-1 homolog B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248934 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein eva-1 homolog C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein eva-1 homolog C measurement http://www.ebi.ac.uk/efo/EFO_0801942 GCST90248935 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet endothelial aggregation receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 platelet endothelial aggregation receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801886 GCST90248936 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet endothelial cell adhesion molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90248937 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxisomal trans-2-enoyl-CoA reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248938 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pigment epithelium-derived factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 pigment epithelium-derived factor measurement http://www.ebi.ac.uk/efo/EFO_0021847 GCST90248939 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peflin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248940 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolyl endopeptidase FAP levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 prolyl endopeptidase FAP measurement http://www.ebi.ac.uk/efo/EFO_0021856 GCST90248941 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase pellino homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 e3 ubiquitin-protein ligase pellino homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0802507 GCST90248942 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proenkephalin-A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 proenkephalin-A measurement http://www.ebi.ac.uk/efo/EFO_0801923 GCST90248943 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase FKBP14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 peptidyl-prolyl cis-trans isomerase FKBP14 measurement http://www.ebi.ac.uk/efo/EFO_0801872 GCST90248944 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase FKBP1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248945 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase FKBP2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 peptidyl-prolyl cis-trans isomerase FKBP2 measurement http://www.ebi.ac.uk/efo/EFO_0802852 GCST90248946 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase FKBP3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248947 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase FKBP4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248948 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase FKBP7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 peptidyl-prolyl cis-trans isomerase FKBP7 measurement http://www.ebi.ac.uk/efo/EFO_0801873 GCST90248949 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248950 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 peptidyl-prolyl cis-trans isomerase H measurement http://www.ebi.ac.uk/efo/EFO_0801874 GCST90248951 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-tRNA hydrolase ICT1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248952 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 peptidyl-prolyl cis-trans isomerase-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801876 GCST90248953 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 peptidyl-prolyl cis-trans isomerase-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801877 GCST90248954 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248955 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase NIMA-interacting 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peptidyl-prolyl cis-trans isomerase NIMA-interacting 4 measurement http://www.ebi.ac.uk/efo/EFO_0801875 GCST90248956 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxisomal 2,4-dienoyl-CoA reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248957 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peregrin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 peregrin measurement http://www.ebi.ac.uk/efo/EFO_0802853 GCST90248958 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Perilipin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248959 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Periostin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90248960 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxiredoxin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 peroxiredoxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020629 GCST90248961 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxiredoxin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 peroxiredoxin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802855 GCST90248962 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PEST proteolytic signal-containing nuclear protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248963 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxisome assembly protein 26 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248964 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostaglandin F2 receptor negative regulator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 prostaglandin F2 receptor negative regulator measurement http://www.ebi.ac.uk/efo/EFO_0801931 GCST90248965 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet factor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248966 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet factor 4 variant levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 platelet factor 4 variant measurement http://www.ebi.ac.uk/efo/EFO_0801887 GCST90248967 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Citrate 243 individuals NA NR [811782] (imputed) 2 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90267462 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of CMP-N-acetylneuraminate 243 individuals NA NR [811782] (imputed) 1 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90267463 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of D-Arabitol 243 individuals NA NR [811782] (imputed) 2 arabitol measurement http://www.ebi.ac.uk/efo/EFO_0800148 GCST90267464 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of D-glucono-1,5-lactone 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267465 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of D-Glucose (mM) (uM) 243 individuals NA NR [811782] (imputed) 1 D-Glucose measurement http://www.ebi.ac.uk/efo/EFO_0021586 GCST90267466 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of D-Glucose 6-phosphate 243 individuals NA NR [811782] (imputed) 3 glucose-6-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010485 GCST90267467 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of D-Rhamnose 243 individuals NA NR [811782] (imputed) 6 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267468 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Dehydroascorbate 243 individuals NA NR [811782] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267469 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Dihomo-g-Linolenic Acid 243 individuals NA NR [811782] (imputed) 1 dihomo-gamma-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007763 GCST90267470 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Diphosphate 243 individuals NA NR [811782] (imputed) 5 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267471 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Docosahexaenoic Acid 243 individuals NA NR [811782] (imputed) 1 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90267472 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Dopamine 243 individuals NA NR [811782] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267473 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of DPA(FA22:5) 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267474 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of ERGOTHIONEINE 243 individuals NA NR [811782] (imputed) 2 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90267475 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Ethyl-Glucoronide 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267476 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of FA 16:1n7 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267477 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of FA18:1 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267478 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of FA18:3-GLA 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267479 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Fructose 1-6-bisphosphate (uM) 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267480 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Fumarate 243 individuals NA NR [811782] (imputed) 13 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90267481 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Gln (uM) 243 individuals NA NR [811782] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90267482 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Glu (uM) 243 individuals NA NR [811782] (imputed) 1 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90267483 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Glutamate 243 individuals NA NR [811782] (imputed) 1 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90267484 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Glycerol 3-phosphate 243 individuals NA NR [811782] (imputed) 1 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90267485 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Glycocholate.1 243 individuals NA NR [811782] (imputed) 1 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90267486 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Hexose phosphate (uM) 243 individuals NA NR [811782] (imputed) 1 hexose measurement http://www.ebi.ac.uk/efo/EFO_0007631 GCST90267487 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Hypoxanthine 243 individuals NA NR [811782] (imputed) 1 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90267488 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Hypoxanthine (uM) 243 individuals NA NR [811782] (imputed) 5 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90267489 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Indole-3-acetate 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267490 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Indole-3-acetate.1 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267491 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Indole.1 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267492 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Indoxyl 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267493 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Inosine 243 individuals NA NR [811782] (imputed) 1 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90267494 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of L-Carnitine 243 individuals NA NR [811782] (imputed) 1 L-Carnitine measurement http://www.ebi.ac.uk/efo/EFO_0021612 GCST90267495 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of L-Carnitine.1 243 individuals NA NR [811782] (imputed) 1 L-Carnitine measurement http://www.ebi.ac.uk/efo/EFO_0021612 GCST90267496 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of L-Noradrenaline 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267497 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of L-Palmitoylcarnitine 243 individuals NA NR [811782] (imputed) 2 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90267498 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Lactate 243 individuals NA NR [811782] (imputed) 2 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90267499 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Lactate (mM) (uM) 243 individuals NA NR [811782] (imputed) 1 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90267500 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Leucine 243 individuals NA NR [811782] (imputed) 1 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90267501 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Linoleic Acid 243 individuals NA NR [811782] (imputed) 1 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90267502 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPC18:2 243 individuals NA NR [811782] (imputed) 1 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90267503 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPI18:1 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267504 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPI20:4 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267505 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPS16:0 243 individuals NA NR [811782] (imputed) 1 lysophosphatidylserine measurement http://www.ebi.ac.uk/efo/EFO_0020048 GCST90267506 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPS18:0 243 individuals NA NR [811782] (imputed) 3 lysophosphatidylserine measurement http://www.ebi.ac.uk/efo/EFO_0020048 GCST90267507 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPS18:1 243 individuals NA NR [811782] (imputed) 1 lysophosphatidylserine measurement http://www.ebi.ac.uk/efo/EFO_0020048 GCST90267508 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPS18:2 243 individuals NA NR [811782] (imputed) 1 lysophosphatidylserine measurement http://www.ebi.ac.uk/efo/EFO_0020048 GCST90267509 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of N-Amidino-L-aspartate 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267510 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of N6-Methyl-L-lysine 243 individuals NA NR [811782] (imputed) 1 N6-Acetyl-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0021656 GCST90267511 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Malate 243 individuals NA NR [811782] (imputed) 1 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90267537 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Malate (uM) 243 individuals NA NR [811782] (imputed) 3 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90267538 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Met (uM) 243 individuals NA NR [811782] (imputed) 2 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90267539 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Methionine 243 individuals NA NR [811782] (imputed) 2 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90267540 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Octadecenoic acid 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267541 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Octanoic acid (caprylate) 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267542 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801956 GCST90249061 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Poliovirus receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 poliovirus receptor measurement http://www.ebi.ac.uk/efo/EFO_0802875 GCST90249062 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PolyUbiquitin K48-linked levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 polyUbiquitin K48-linked measurement http://www.ebi.ac.uk/efo/EFO_0022007 GCST90249063 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PolyUbiquitin K63-linked levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 polyUbiquitin K63-linked measurement http://www.ebi.ac.uk/efo/EFO_0022008 GCST90249064 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Poly(A) polymerase gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 poly(A) polymerase gamma measurement http://www.ebi.ac.uk/efo/EFO_0802878 GCST90249065 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Poly(A) RNA polymerase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 poly(A) RNA polymerase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801893 GCST90249066 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Poly(ADP-ribose) glycohydrolase ARH3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249067 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Poly(rC)-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 poly(rC)-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801894 GCST90249068 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Poly(U)-specific endoribonuclease levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 poly(U)-specific endoribonuclease measurement http://www.ebi.ac.uk/efo/EFO_0802879 GCST90249069 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Poly(U)-binding-splicing factor PUF60 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 poly(U)-binding-splicing factor PUF60 measurement http://www.ebi.ac.uk/efo/EFO_0801895 GCST90249070 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein O-mannose kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249071 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxisomal carnitine O-octanoyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peroxisomal carnitine O-octanoyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802856 GCST90249072 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proto-oncogene tyrosine-protein kinase receptor Ret levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 proto-oncogene tyrosine-protein kinase receptor Ret measurement http://www.ebi.ac.uk/efo/EFO_0008272 GCST90249073 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proto-oncogene tyrosine-protein kinase ROS levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249074 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proto-oncogene tyrosine-protein kinase Src levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 proto-oncogene tyrosine-protein kinase Src measurement http://www.ebi.ac.uk/efo/EFO_0010927 GCST90249075 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. POTE ankyrin domain family member G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249076 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein phosphatase 1 regulatory subunit 14A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249077 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein phosphatase 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein phosphatase 1A measurement http://www.ebi.ac.uk/efo/EFO_0802957 GCST90249078 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein phosphatase 1D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249079 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein phosphatase 1L levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein phosphatase 1L measurement http://www.ebi.ac.uk/efo/EFO_0802958 GCST90249080 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxisome proliferator-activated receptor alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 peroxisome proliferator-activated receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0802858 GCST90249081 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoserine aminotransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249082 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Putative phospholipase B-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 putative phospholipase B-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0802982 GCST90249083 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alkaline phosphatase, placental-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249084 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidate phosphatase PPAPDC1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 phosphatidate phosphatase PPAPDC1A measurement http://www.ebi.ac.uk/efo/EFO_0802860 GCST90249085 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phospholipid transfer protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249036 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin-A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 plexin-A1 measurement http://www.ebi.ac.uk/efo/EFO_0801892 GCST90249037 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin-A4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249038 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin-B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 plexin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0021867 GCST90249039 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin-B3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249040 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin-C1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 plexin-C1 measurement http://www.ebi.ac.uk/efo/EFO_0008266 GCST90249041 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin-D1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249042 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein max levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249043 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanocyte protein PMEL levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 melanocyte protein PMEL measurement http://www.ebi.ac.uk/efo/EFO_0801792 GCST90249044 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphomannomutase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249045 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphomannomutase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249046 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mismatch repair endonuclease PMS2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 mismatch repair endonuclease PMS2 measurement http://www.ebi.ac.uk/efo/EFO_0802748 GCST90249047 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphomevalonate kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 phosphomevalonate kinase measurement http://www.ebi.ac.uk/efo/EFO_0801883 GCST90249048 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polypeptide N-acetylgalactosaminyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 polypeptide N-acetylgalactosaminyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801899 GCST90249049 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polypeptide N-acetylgalactosaminyltransferase 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 polypeptide N-acetylgalactosaminyltransferase 11 measurement http://www.ebi.ac.uk/efo/EFO_0802883 GCST90249050 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polypeptide N-acetylgalactosaminyltransferase 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 polypeptide N-acetylgalactosaminyltransferase 16 measurement http://www.ebi.ac.uk/efo/EFO_0801900 GCST90249051 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polypeptide N-acetylgalactosaminyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 polypeptide N-acetylgalactosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802884 GCST90249052 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polypeptide N-acetylgalactosaminyltransferase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 polypeptide N-acetylgalactosaminyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802885 GCST90249053 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bifunctional polynucleotide phosphatase/kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 bifunctional polynucleotide phosphatase/kinase measurement http://www.ebi.ac.uk/efo/EFO_0801424 GCST90249054 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prepronociceptin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249055 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Palmitoleoyl-protein carboxylesterase NOTUM levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 palmitoleoyl-protein carboxylesterase NOTUM measurement http://www.ebi.ac.uk/efo/EFO_0802842 GCST90249056 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Purine nucleoside phosphorylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249057 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pro-neuregulin-2, membrane-bound isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pro-neuregulin-2, membrane-bound isoform measurement http://www.ebi.ac.uk/efo/EFO_0802900 GCST90249058 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein O-glucosyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein O-glucosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801955 GCST90249059 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polycystin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 polycystin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802881 GCST90249060 Genome-wide genotyping array 2023-07-10 35589828 Kim S 2022-05-19 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/35589828 Shared genetic architectures of subjective well-being in East Asian and European ancestry populations. Subjective well-being 311,126 European ancestry individuals NA NR [4507044] (imputed) 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90104898 Genome-wide genotyping array 2023-07-10 35589828 Kim S 2022-05-19 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/35589828 Shared genetic architectures of subjective well-being in East Asian and European ancestry populations. Subjective well-being 110,919 Korean ancestry individuals, 563,176 European ancestry individuals NA NR [NR] (imputed) 40 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90128421 Genome-wide genotyping array 2023-07-10 35589828 Kim S 2022-05-19 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/35589828 Shared genetic architectures of subjective well-being in East Asian and European ancestry populations. Subjective well-being 563,176 European ancestry individuals NA NR [NR] (imputed) 14 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90128422 Genome-wide genotyping array 2023-07-10 35589828 Kim S 2022-05-19 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/35589828 Shared genetic architectures of subjective well-being in East Asian and European ancestry populations. Subjective well-being 110,919 Korean ancestry individuals, 311,126 European ancestry individuals NA NR [2223649] (imputed) 0 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90271789 Genome-wide genotyping array 2023-07-10 35589828 Kim S 2022-05-19 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/35589828 Shared genetic architectures of subjective well-being in East Asian and European ancestry populations. Subjective well-being 110,919 Korean ancestry individuals NA NR [6825852] (imputed) 3 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90104897 Genome-wide genotyping array 2023-06-28 37116407 Park S 2023-02-18 Nutrition www.ncbi.nlm.nih.gov/pubmed/37116407 Association of polygenic risk scores for insulin resistance risk and their interaction with a plant-based diet, especially fruits, vitamin C, and flavonoid intake, in Asian adults. Insulin resistance 58,701 East Asian ancestry individuals NA NR [NR] 10 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90271574 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Butyrophilin subfamily 2 member A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246749 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Butyrophilin subfamily 3 member A3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246750 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Betacellulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 betacellulin measurement http://www.ebi.ac.uk/efo/EFO_0021883 GCST90246751 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein BTG2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246752 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-thromboglobulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246753 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B- and T-lymphocyte attenuator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246754 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Butyrophilin-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246755 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Butyrophilin-like protein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246756 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Butyrophilin-like protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 butyrophilin-like protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0802341 GCST90246757 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitotic checkpoint serine/threonine-protein kinase BUB1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 mitotic checkpoint serine/threonine-protein kinase BUB1 measurement http://www.ebi.ac.uk/efo/EFO_0801806 GCST90246758 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C1GALT1-specific chaperone 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 C1GALT1-specific chaperone 1 measurement http://www.ebi.ac.uk/efo/EFO_0801437 GCST90246759 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1q subcomponent levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90246760 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement component 1 Q subcomponent-binding protein, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement component 1 q subcomponent-binding protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020280 GCST90246761 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1q subcomponent subunit C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 complement C1q subcomponent subunit C measurement http://www.ebi.ac.uk/efo/EFO_0801492 GCST90246762 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1q-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246763 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement component C1q receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 complement component C1q receptor measurement http://www.ebi.ac.uk/efo/EFO_0802427 GCST90246764 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C1q-related factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246765 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1q tumor necrosis factor-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 complement C1q tumor necrosis factor-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801493 GCST90246766 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1q tumor necrosis factor-related protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 complement C1q tumor necrosis factor-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802425 GCST90246767 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1q tumor necrosis factor-related protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 complement C1q tumor necrosis factor-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801494 GCST90246768 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1q and tumor necrosis factor-related protein 9A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement C1q and tumor necrosis factor-related protein 9A measurement http://www.ebi.ac.uk/efo/EFO_0803293 GCST90246769 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1r subcomponent levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement C1r subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008090 GCST90246770 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1r subcomponent-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 complement C1r subcomponent-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801495 GCST90246771 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C1s subcomponent levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 complement C1s subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008091 GCST90246772 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-1-tetrahydrofolate synthase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246773 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gastric intrinsic factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247731 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gigaxonin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 gigaxonin measurement http://www.ebi.ac.uk/efo/EFO_0802566 GCST90247732 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gastric inhibitory polypeptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247733 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycosyltransferase 8 domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glycosyltransferase 8 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801648 GCST90247734 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glia-derived nexin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glia-derived nexin measurement http://www.ebi.ac.uk/efo/EFO_0020403 GCST90247735 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glioma pathogenesis-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glioma pathogenesis-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802567 GCST90247736 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutamine synthetase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247737 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucagon-like peptide 1 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glucagon-like peptide 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0802568 GCST90247738 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycolipid transfer protein domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 glycolipid transfer protein domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801643 GCST90247739 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucosidase 2 subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glucosidase 2 subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801628 GCST90247740 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucose-6-phosphate isomerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glucose-6-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020407 GCST90247741 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutamyl aminopeptidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247742 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucokinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247743 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutaredoxin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247744 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutaredoxin-2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glutaredoxin-2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801633 GCST90247745 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutaredoxin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247746 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase Mu 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 glutathione S-transferase Mu 1 measurement http://www.ebi.ac.uk/efo/EFO_0801638 GCST90247747 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase Mu 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247748 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase Mu 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247749 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase P levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90247750 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione reductase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247751 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase theta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247752 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247753 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glyceraldehyde-3-phosphate dehydrogenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glyceraldehyde-3-phosphate dehydrogenase measurement http://www.ebi.ac.uk/efo/EFO_0020411 GCST90247754 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glypican-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glypican-1 measurement http://www.ebi.ac.uk/efo/EFO_0801649 GCST90247755 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247706 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 11/8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 growth/differentiation factor 11/8 measurement http://www.ebi.ac.uk/efo/EFO_0021962 GCST90247707 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247708 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 growth/differentiation factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020428 GCST90247709 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247710 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 growth/differentiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020429 GCST90247711 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247712 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth/differentiation factor 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 growth/differentiation factor 8 measurement http://www.ebi.ac.uk/efo/EFO_0021960 GCST90247713 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GDH/6PGL endoplasmic bifunctional protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 10 GDH/6PGL endoplasmic bifunctional protein measurement http://www.ebi.ac.uk/efo/EFO_0801619 GCST90247714 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GDP-fucose protein O-fucosyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 GDP-fucose protein O-fucosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801621 GCST90247715 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gelsolin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 gelsolin measurement http://www.ebi.ac.uk/efo/EFO_0020402 GCST90247716 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycoprotein endo-alpha-1,2-mannosidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glycoprotein endo-alpha-1,2-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801644 GCST90247717 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glial fibrillary acidic protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90247718 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GDNF family receptor alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 gdnf family receptor alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020400 GCST90247719 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GDNF family receptor alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 GDNF family receptor alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0008138 GCST90247720 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GDNF family receptor alpha-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 gdnf family receptor alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020401 GCST90247721 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GDNF family receptor alpha-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 GDNF family receptor alpha-like measurement http://www.ebi.ac.uk/efo/EFO_0801620 GCST90247722 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-binding protein GGA1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ADP-ribosylation factor-binding protein GGA1 measurement http://www.ebi.ac.uk/efo/EFO_0801352 GCST90247723 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-binding protein GGA3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ADP-ribosylation factor-binding protein GGA3 measurement http://www.ebi.ac.uk/efo/EFO_0801353 GCST90247724 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. G antigen 2D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247725 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-glutamyl hydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 gamma-glutamyl hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0801616 GCST90247726 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ganglioside GM2 activator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247727 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Geranylgeranyl pyrophosphate synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247728 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth hormone receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247729 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTPase HRas levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247730 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinol-binding protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249257 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoid-binding protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 retinoid-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802006 GCST90249258 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribosome biogenesis protein TSR3 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ribosome biogenesis protein TSR3 homolog measurement http://www.ebi.ac.uk/efo/EFO_0803025 GCST90249259 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RAC-beta serine/threonine-protein kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 RAC-beta serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021989 GCST90249260 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribokinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249261 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retina-specific copper amine oxidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 retina-specific copper amine oxidase measurement http://www.ebi.ac.uk/efo/EFO_0803011 GCST90249262 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-binding cancer antigen expressed on SiSo cells levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249263 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell differentiation protein RCD1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cell differentiation protein RCD1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0802383 GCST90249264 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 2-deoxynucleoside 5-phosphate N-hydrolase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249265 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Reticulocalbin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249266 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rieske domain-containing protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 rieske domain-containing protein measurement http://www.ebi.ac.uk/efo/EFO_0802026 GCST90249267 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinal dehydrogenase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249268 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinol dehydrogenase 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 retinol dehydrogenase 16 measurement http://www.ebi.ac.uk/efo/EFO_0802007 GCST90249269 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonucleoside-diphosphate reductase large subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ribonucleoside-diphosphate reductase large subunit measurement http://www.ebi.ac.uk/efo/EFO_0802021 GCST90249270 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonucleoside-diphosphate reductase subunit M2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249271 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonucleoside-diphosphate reductase subunit M2 B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ribonucleoside-diphosphate reductase subunit M2 B measurement http://www.ebi.ac.uk/efo/EFO_0802022 GCST90249272 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Recoverin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 recoverin measurement http://www.ebi.ac.uk/efo/EFO_0803003 GCST90249273 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Red levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249274 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regenerating islet-derived protein 3-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 regenerating islet-derived protein 3-alpha measurement http://www.ebi.ac.uk/efo/EFO_0803004 GCST90249275 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regenerating islet-derived protein 3-gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249276 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regenerating islet-derived protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 regenerating islet-derived protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021921 GCST90249277 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Relaxin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249278 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RELT-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 RELT-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802000 GCST90249279 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RELT-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 RELT-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803008 GCST90249280 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Renin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 renin measurement http://www.ebi.ac.uk/efo/EFO_0010616 GCST90249281 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249207 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ras-related protein Rab-14 measurement http://www.ebi.ac.uk/efo/EFO_0801988 GCST90249208 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249209 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249210 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249211 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-26 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 ras-related protein Rab-26 measurement http://www.ebi.ac.uk/efo/EFO_0801989 GCST90249212 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249213 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-2B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249214 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-31 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249215 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-35 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ras-related protein Rab-35 measurement http://www.ebi.ac.uk/efo/EFO_0801990 GCST90249216 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-39B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ras-related protein Rab-39B measurement http://www.ebi.ac.uk/efo/EFO_0802994 GCST90249217 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249218 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-4A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249219 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-5A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249220 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-5B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249221 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-5C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249222 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-6B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249223 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RAB6-interacting golgin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RAB6-interacting Golgin measurement http://www.ebi.ac.uk/efo/EFO_0801983 GCST90249224 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-7b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ras-related protein Rab-7b measurement http://www.ebi.ac.uk/efo/EFO_0802995 GCST90249225 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rab9 effector protein with kelch motifs levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 rab9 effector protein with kelch motifs measurement http://www.ebi.ac.uk/efo/EFO_0801984 GCST90249226 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rab GDP dissociation inhibitor beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 rab gdp dissociation inhibitor beta measurement http://www.ebi.ac.uk/efo/EFO_0020697 GCST90249227 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cellular retinoic acid-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 cellular retinoic acid-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801463 GCST90249228 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cellular retinoic acid-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cellular retinoic acid-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802386 GCST90249229 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related C3 botulinum toxin substrate 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ras-related C3 botulinum toxin substrate 3 measurement http://www.ebi.ac.uk/efo/EFO_0021987 GCST90249230 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA repair protein RAD51 homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 DNA repair protein rad51 homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0020330 GCST90249231 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA repair protein RAD51 homolog 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 DNA repair protein RAD51 homolog 4 measurement http://www.ebi.ac.uk/efo/EFO_0801531 GCST90249232 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Radixin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249233 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Ral-A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249234 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Ral-B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249235 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor activity-modifying protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249236 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ran-binding protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ran-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802988 GCST90249237 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ran-specific GTPase-activating protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249238 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. alpha-2-macroglobulin receptor-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90249239 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rap-2a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ras-related protein Rap-2a measurement http://www.ebi.ac.uk/efo/EFO_0802996 GCST90249240 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RAC-alpha serine/threonine-protein kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249241 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein M-Ras levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249242 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-11A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249243 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-22A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ras-related protein Rab-22A measurement http://www.ebi.ac.uk/efo/EFO_0802991 GCST90249244 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-27A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ras-related protein Rab-27A measurement http://www.ebi.ac.uk/efo/EFO_0802992 GCST90249245 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein Rab-27B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ras-related protein Rab-27B measurement http://www.ebi.ac.uk/efo/EFO_0802993 GCST90249246 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-binding protein RBBP4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249247 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA binding protein fox-1 homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RNA binding protein fox-1 homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0803033 GCST90249248 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoblastoma-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 retinoblastoma-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803013 GCST90249249 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoblastoma-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249250 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pre-mRNA-splicing factor RBM22 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249251 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA-binding protein 24 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 RNA-binding protein 24 measurement http://www.ebi.ac.uk/efo/EFO_0802030 GCST90249252 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA-binding protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 RNA-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802031 GCST90249253 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA-binding protein 40 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RNA-binding protein 40 measurement http://www.ebi.ac.uk/efo/EFO_0803037 GCST90249254 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinol-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249255 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinol-binding protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 retinol-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020707 GCST90249256 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 regulator of G-protein signaling 3 measurement http://www.ebi.ac.uk/efo/EFO_0803006 GCST90249305 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249306 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249307 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249308 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 regulator of G-protein signaling 8 measurement http://www.ebi.ac.uk/efo/EFO_0801997 GCST90249309 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rac GTPase-activating protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 rac GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801985 GCST90249310 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho GTPase-activating protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 rho GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803015 GCST90249311 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho GTPase-activating protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 rho GTPase-activating protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803017 GCST90249312 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho GTPase-activating protein 25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 rho GTPase-activating protein 25 measurement http://www.ebi.ac.uk/efo/EFO_0802011 GCST90249313 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho GTPase-activating protein 30 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 rho GTPase-activating protein 30 measurement http://www.ebi.ac.uk/efo/EFO_0802012 GCST90249314 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho GTPase-activating protein 36 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 rho GTPase-activating protein 36 measurement http://www.ebi.ac.uk/efo/EFO_0803016 GCST90249315 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho-related GTP-binding protein Rho6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 rho-related GTP-binding protein Rho6 measurement http://www.ebi.ac.uk/efo/EFO_0803022 GCST90249316 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho-related GTP-binding protein RhoB levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249317 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho-related GTP-binding protein RhoC levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249318 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho-related GTP-binding protein RhoD levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 rho-related GTP-binding protein RhoD measurement http://www.ebi.ac.uk/efo/EFO_0803023 GCST90249319 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rhophilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 rhophilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802015 GCST90249320 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein RIC-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein RIC-3 measurement http://www.ebi.ac.uk/efo/EFO_0801957 GCST90249321 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Radiation-inducible immediate-early gene IEX-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 radiation-inducible immediate-early gene IEX-1 measurement http://www.ebi.ac.uk/efo/EFO_0802987 GCST90249322 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Riboflavin kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 riboflavin kinase measurement http://www.ebi.ac.uk/efo/EFO_0802016 GCST90249323 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-interacting serine/threonine-protein kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 receptor-interacting serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802997 GCST90249324 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RISC-loading complex subunit TARBP2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249325 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 60S ribosomal protein L12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249326 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 60S ribosomal protein L30 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 60S ribosomal protein L30 measurement http://www.ebi.ac.uk/efo/EFO_0801337 GCST90249327 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retroviral-like aspartic protease 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 retroviral-like aspartic protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0802008 GCST90249328 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinaldehyde-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 retinaldehyde-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802003 GCST90249329 Genome-wide genotyping array 2023-08-03 37015192 Men X 2023-04-04 Neuropsychobiology www.ncbi.nlm.nih.gov/pubmed/37015192 Genomic Investigation of Remission and Relapse of Psychotic Depression Treated with Sertraline plus Olanzapine: The STOP-PD II Study. Remission after sertraline plus olanzapine treatment in psychotic depression 94 European ancestry remission cases, 49 European ancestry non-remission controls, 14 African ancestry remission cases, 3 African ancestry non-remission controls, 7 remission cases, 4 non-remission controls NA Illumina [4261750] (imputed) 5 response to sertraline, psychotic symptom measurement, response to olanzapine http://www.ebi.ac.uk/efo/EFO_0006327, http://www.ebi.ac.uk/efo/EFO_0009182, http://purl.obolibrary.org/obo/GO_0097333 GCST90275121 Genome-wide genotyping array 2023-08-03 37015192 Men X 2023-04-04 Neuropsychobiology www.ncbi.nlm.nih.gov/pubmed/37015192 Genomic Investigation of Remission and Relapse of Psychotic Depression Treated with Sertraline plus Olanzapine: The STOP-PD II Study. Relapse of psychotic depression after sertraline plus olanzapine treatment 27 European ancestry relapse cases, 46 European ancestry non-relapse controls, 6 African ancestry relapse cases, 2 African ancestry non-relapse controls, 1 relapse case, 5 non-relapse controls NA Illumina [4261750] (imputed) 0 major depressive episode, response to sertraline, psychotic symptom measurement, response to olanzapine http://www.ebi.ac.uk/efo/EFO_0007634, http://www.ebi.ac.uk/efo/EFO_0006327, http://www.ebi.ac.uk/efo/EFO_0009182, http://purl.obolibrary.org/obo/GO_0097333 GCST90275122 Genome-wide genotyping array 2023-08-03 37015192 Men X 2023-04-04 Neuropsychobiology www.ncbi.nlm.nih.gov/pubmed/37015192 Genomic Investigation of Remission and Relapse of Psychotic Depression Treated with Sertraline plus Olanzapine: The STOP-PD II Study. Remission after sertraline plus olanzapine treatment in psychotic depression 94 European ancestry remission cases, 49 European ancestry non-remission controls NA Illumina [4261750] (imputed) 1 response to sertraline, psychotic symptom measurement, response to olanzapine http://www.ebi.ac.uk/efo/EFO_0006327, http://www.ebi.ac.uk/efo/EFO_0009182, http://purl.obolibrary.org/obo/GO_0097333 GCST90275123 Genome-wide genotyping array 2023-08-03 37015192 Men X 2023-04-04 Neuropsychobiology www.ncbi.nlm.nih.gov/pubmed/37015192 Genomic Investigation of Remission and Relapse of Psychotic Depression Treated with Sertraline plus Olanzapine: The STOP-PD II Study. Relapse of psychotic depression after sertraline plus olanzapine treatment 27 European ancestry relapse cases, 46 European ancestry non-relapse controls NA Illumina [4261750] (imputed) 0 major depressive episode, response to sertraline, psychotic symptom measurement, response to olanzapine http://www.ebi.ac.uk/efo/EFO_0007634, http://www.ebi.ac.uk/efo/EFO_0006327, http://www.ebi.ac.uk/efo/EFO_0009182, http://purl.obolibrary.org/obo/GO_0097333 GCST90275124 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 receptor antagonist protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-1 receptor antagonist protein measurement http://www.ebi.ac.uk/efo/EFO_0801712 GCST90248050 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 receptor-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 interleukin-1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801713 GCST90248051 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 receptor-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interleukin-1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801714 GCST90248052 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 receptor type 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90248053 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 receptor type 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90248054 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-20 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-20 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020497 GCST90248055 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-20 receptor subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248056 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-21 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-21 measurement http://www.ebi.ac.uk/efo/EFO_0801724 GCST90248057 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-22 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90248058 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-22 receptor subunit alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90248059 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-22 receptor subunit alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90248060 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90248061 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-23 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interleukin-23 receptor measurement http://www.ebi.ac.uk/efo/EFO_0801725 GCST90248062 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-25 measurement http://www.ebi.ac.uk/efo/EFO_0801726 GCST90248063 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-26 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248064 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-27 measurement http://www.ebi.ac.uk/efo/EFO_0010916 GCST90248065 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-27 subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248066 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-27 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-27 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801727 GCST90248067 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-2 receptor subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interleukin-2 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0802657 GCST90248068 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-31 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-31 measurement http://www.ebi.ac.uk/efo/EFO_0801728 GCST90248069 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-34 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 interleukin-34 measurement http://www.ebi.ac.uk/efo/EFO_0020505 GCST90248070 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-36 alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-36 alpha measurement http://www.ebi.ac.uk/efo/EFO_0021851 GCST90248071 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-36 receptor antagonist protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248072 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-37 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 interleukin-37 measurement http://www.ebi.ac.uk/efo/EFO_0020506 GCST90248073 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-3 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90248074 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-5 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 interleukin-5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801730 GCST90248075 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-6 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801731 GCST90248076 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-6 receptor subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 interleukin-6 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801732 GCST90248077 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-7 measurement http://www.ebi.ac.uk/efo/EFO_0802662 GCST90248078 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-7 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-7 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020508 GCST90248079 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST90248080 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interleukin-9 measurement http://www.ebi.ac.uk/efo/EFO_0802663 GCST90248081 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin enhancer-binding factor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin enhancer-binding factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802652 GCST90248082 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integrin-linked protein kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248083 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Importin subunit alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 importin subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020467 GCST90248084 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Importin subunit alpha-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 importin subunit alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0802623 GCST90248085 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Importin subunit alpha-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248086 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating measurement http://www.ebi.ac.uk/efo/EFO_0802092 GCST90249415 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serum amyloid A-1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90249416 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serum amyloid A-2 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249417 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serum amyloid A-4 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249418 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sperm acrosome-associated protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249419 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sperm acrosome membrane-associated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249420 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sperm acrosome membrane-associated protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sperm acrosome membrane-associated protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802081 GCST90249421 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SUMO-activating enzyme subunit 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249422 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenosylhomocysteinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249423 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serum albumin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90249424 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Deoxynucleoside triphosphate triphosphohydrolase SAMHD1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 deoxynucleoside triphosphate triphosphohydrolase SAMHD1 measurement http://www.ebi.ac.uk/efo/EFO_0802459 GCST90249425 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serum amyloid P-component levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serum amyloid P-component measurement http://www.ebi.ac.uk/efo/EFO_0008283 GCST90249426 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone deacetylase complex subunit SAP18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histone deacetylase complex subunit SAP18 measurement http://www.ebi.ac.uk/efo/EFO_0801680 GCST90249427 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-induced gene 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 insulin-induced gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802629 GCST90248025 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-10 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 interleukin-10 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0021890 GCST90248026 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-10 receptor subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interleukin-10 receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020489 GCST90248027 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-11 measurement http://www.ebi.ac.uk/efo/EFO_0020490 GCST90248028 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-11 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-11 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020491 GCST90248029 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-12 subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248030 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-12 receptor subunit beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0801715 GCST90248031 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-13 measurement http://www.ebi.ac.uk/efo/EFO_0802655 GCST90248032 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-13 receptor subunit alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-13 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020493 GCST90248033 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248034 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-15 receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 interleukin-15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801716 GCST90248035 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-16 measurement http://www.ebi.ac.uk/efo/EFO_0801717 GCST90248036 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-17A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90248037 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-17B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-17B measurement http://www.ebi.ac.uk/efo/EFO_0021973 GCST90248038 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-17C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-17C measurement http://www.ebi.ac.uk/efo/EFO_0802656 GCST90248039 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-17F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interleukin-17F measurement http://www.ebi.ac.uk/efo/EFO_0021963 GCST90248040 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-17 receptor A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 interleukin-17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0801718 GCST90248041 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. interleukin-17 receptor B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 interleukin-17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0801719 GCST90248042 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-17 receptor D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interleukin-17 receptor D measurement http://www.ebi.ac.uk/efo/EFO_0801720 GCST90248043 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. interleukin-18 receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 interleukin-18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801721 GCST90248044 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-18 receptor accessory protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248045 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 interleukin-19 measurement http://www.ebi.ac.uk/efo/EFO_0801722 GCST90248046 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST90248047 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST90248048 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 Receptor accessory protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 interleukin-1 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0801711 GCST90248049 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interleukin-1 receptor-associated kinase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248122 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon regulatory factor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248123 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon regulatory factor 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interferon regulatory factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0802650 GCST90248124 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive ribonuclease-like protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 inactive ribonuclease-like protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0802626 GCST90248125 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kin of IRRE-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 kin of IRRE-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802678 GCST90248126 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kin of IRRE-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 kin of IRRE-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020521 GCST90248127 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Iron-sulfur cluster assembly enzyme ISCU, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 iron-sulfur cluster assembly enzyme ISCU, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802665 GCST90248128 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin superfamily containing leucine-rich repeat protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 immunoglobulin superfamily containing leucine-rich repeat protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021879 GCST90248129 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isthmin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 isthmin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801737 GCST90248130 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isochorismatase domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 isochorismatase domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801735 GCST90248131 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive serine protease 35 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248132 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integrin alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248133 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integrin alpha-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 integrin alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802637 GCST90248134 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase Itchy homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248135 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intestinal-type alkaline phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 intestinal-type alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0801734 GCST90248136 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integral membrane protein 2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 integral membrane protein 2A measurement http://www.ebi.ac.uk/efo/EFO_0801704 GCST90248137 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integral membrane protein 2B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 integral membrane protein 2B measurement http://www.ebi.ac.uk/efo/EFO_0802634 GCST90248138 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inosine triphosphate pyrophosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248139 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive tyrosine-protein kinase 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248140 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intersectin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 intersectin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801733 GCST90248141 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein jagged-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein jagged-1 measurement http://www.ebi.ac.uk/efo/EFO_0008271 GCST90248142 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Junctional adhesion molecule C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 junctional adhesion molecule C measurement http://www.ebi.ac.uk/efo/EFO_0020510 GCST90248143 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Junctional adhesion molecule-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 junctional adhesion molecule-like measurement http://www.ebi.ac.uk/efo/EFO_0020511 GCST90248144 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Janus kinase and microtubule-interacting protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 janus kinase and microtubule-interacting protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801738 GCST90248145 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bifunctional arginine demethylase and lysyl-hydroxylase JMJD6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248146 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 72 kDa inositol polyphosphate 5-phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 72 kDa inositol polyphosphate 5-phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0802244 GCST90248097 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like peptide INSL5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 insulin-like peptide INSL5 measurement http://www.ebi.ac.uk/efo/EFO_0802632 GCST90248098 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like peptide INSL6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 insulin-like peptide INSL6 measurement http://www.ebi.ac.uk/efo/EFO_0802633 GCST90248099 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 insulin-like 3 measurement http://www.ebi.ac.uk/efo/EFO_0802630 GCST90248100 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integrin alpha-I: beta-1 complex levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 integrin alpha-I: beta-1 complex measurement http://www.ebi.ac.uk/efo/EFO_0008162 GCST90248101 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integrin alpha-IIb: beta-3 complex levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 integrin alpha-IIb: beta-3 complex measurement http://www.ebi.ac.uk/efo/EFO_0020479 GCST90248102 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intercellular adhesion molecule 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 intercellular adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0801707 GCST90248103 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intercellular adhesion molecule 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90248104 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intercellular adhesion molecule 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 intercellular adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020482 GCST90248105 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intercellular adhesion molecule 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 intercellular adhesion molecule 4 measurement http://www.ebi.ac.uk/efo/EFO_0801708 GCST90248106 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intercellular adhesion molecule 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 11 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90248107 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integrin beta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248108 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Integrin beta-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248109 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interstitial collagenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 interstitial collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008193 GCST90248110 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intelectin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248111 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol oxygenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248112 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol-trisphosphate 3-kinase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 inositol-trisphosphate 3-kinase A measurement http://www.ebi.ac.uk/efo/EFO_0802627 GCST90248113 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol-trisphosphate 3-kinase C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248114 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive phospholipase D5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 inactive phospholipase D5 measurement http://www.ebi.ac.uk/efo/EFO_0802625 GCST90248115 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive pancreatic lipase-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 inactive pancreatic lipase-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801693 GCST90248116 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inorganic pyrophosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 inorganic pyrophosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008157 GCST90248117 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inorganic pyrophosphatase 2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248118 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. IQ domain-containing protein F1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 IQ domain-containing protein F1 measurement http://www.ebi.ac.uk/efo/EFO_0802664 GCST90248119 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. IQ domain-containing protein F3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248120 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 insulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008160 GCST90248121 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kynureninase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 kynureninase measurement http://www.ebi.ac.uk/efo/EFO_0008201 GCST90248219 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kynurenine--oxoglutarate transaminase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248220 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kynurenine--oxoglutarate transaminase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 kynurenine--oxoglutarate transaminase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801752 GCST90248221 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Left-right determination factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248222 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Extracellular glycoprotein lacritin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248223 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactosylceramide 4-alpha-galactosyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 lactosylceramide 4-alpha-galactosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802683 GCST90248224 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactosylceramide alpha-2,3-sialyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248225 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactadherin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 lactadherin measurement http://www.ebi.ac.uk/efo/EFO_0008203 GCST90248226 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactoylglutathione lyase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 lactoylglutathione lyase measurement http://www.ebi.ac.uk/efo/EFO_0802684 GCST90248227 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactoperoxidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 lactoperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0020525 GCST90248228 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactotransferrin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 lactotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020526 GCST90248229 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Long-chain specific acyl-CoA dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248230 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ladinin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ladinin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802685 GCST90248231 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low affinity immunoglobulin epsilon Fc receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 low affinity immunoglobulin epsilon Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0008210 GCST90248232 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphocyte activation gene 3 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 lymphocyte activation gene 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0020540 GCST90248233 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte-associated immunoglobulin-like receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leukocyte-associated immunoglobulin-like receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802706 GCST90248234 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte-associated immunoglobulin-like receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248235 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Laminin subunit alpha-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 laminin subunit alpha-4 measurement http://www.ebi.ac.uk/efo/EFO_0801755 GCST90248236 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Laminin subunit gamma-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 laminin subunit gamma-2 measurement http://www.ebi.ac.uk/efo/EFO_0801756 GCST90248237 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Laminin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248238 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248239 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ragulator complex protein LAMTOR2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248240 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ragulator complex protein LAMTOR3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ragulator complex protein LAMTOR3 measurement http://www.ebi.ac.uk/efo/EFO_0801986 GCST90248241 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. LanC-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248242 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lamina-associated polypeptide 2, isoforms beta/gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lamina-associated polypeptide 2, isoforms beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0801754 GCST90248243 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin H1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249626 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sphingosine kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 sphingosine kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020750 GCST90249627 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sphingosine kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sphingosine kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020751 GCST90249628 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin I2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serpin I2 measurement http://www.ebi.ac.uk/efo/EFO_0803068 GCST90249629 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249630 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine protease inhibitor Kazal-type 13 measurement http://www.ebi.ac.uk/efo/EFO_0803057 GCST90249631 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249632 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 serine protease inhibitor Kazal-type 2 measurement http://www.ebi.ac.uk/efo/EFO_0802054 GCST90249633 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249634 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine protease inhibitor Kazal-type 5 measurement http://www.ebi.ac.uk/efo/EFO_0803058 GCST90249635 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine protease inhibitor Kazal-type 6 measurement http://www.ebi.ac.uk/efo/EFO_0802055 GCST90249636 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249637 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease inhibitor Kazal-type 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine protease inhibitor Kazal-type 9 measurement http://www.ebi.ac.uk/efo/EFO_0803060 GCST90249638 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Spindlin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249639 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Snurportin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249640 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Spondin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90249641 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Spondin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249642 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sprouty-related, EVH1 domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sprouty-related, EVH1 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803102 GCST90249643 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Shadow of prion protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249644 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Selenide, water dikinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 selenide, water dikinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802045 GCST90249645 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SPRY domain-containing SOCS box protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 SPRY domain-containing SOCS box protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803103 GCST90249646 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Spermine synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249647 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Spermatogenesis-associated protein 20 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 spermatogenesis-associated protein 20 measurement http://www.ebi.ac.uk/efo/EFO_0802083 GCST90249648 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine palmitoyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine palmitoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803055 GCST90249649 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine palmitoyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine palmitoyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0803056 GCST90249650 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Steroid receptor RNA activator 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249651 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein SERAC1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein SERAC1 measurement http://www.ebi.ac.uk/efo/EFO_0801963 GCST90249652 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sarcalumenin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249653 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sarcoplasmic reticulum histidine-rich calcium-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249654 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine-rich single-pass membrane protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine-rich single-pass membrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802056 GCST90249655 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal recognition particle 19 kDa protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249656 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfiredoxin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sulfiredoxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802101 GCST90249657 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Somatostatin-28 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 somatostatin-28 measurement http://www.ebi.ac.uk/efo/EFO_0020745 GCST90249658 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Succinate-semialdehyde dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249659 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. FACT complex subunit SSRP1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fact complex subunit ssrp1 measurement http://www.ebi.ac.uk/efo/EFO_0020371 GCST90249660 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sperm surface protein Sp17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249661 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA polymerase II subunit A C-terminal domain phosphatase SSU72 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RNA polymerase II subunit A C-terminal domain phosphatase SSU72 measurement http://www.ebi.ac.uk/efo/EFO_0802029 GCST90249662 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfotransferase 1A3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249663 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfotransferase family cytosolic 1B member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249664 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfotransferase 1C2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249665 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfotransferase family cytosolic 2B member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249666 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfotransferase 4A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sulfotransferase 4A1 measurement http://www.ebi.ac.uk/efo/EFO_0803108 GCST90249667 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal transducer and activator of transcription 5B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249668 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stabilin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 stabilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802086 GCST90249669 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stabilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 stabilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020752 GCST90249670 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratinocyte differentiation-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 keratinocyte differentiation-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801743 GCST90248214 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kunitz-type protease inhibitor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 Kunitz-type protease inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008199 GCST90248215 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kunitz-type protease inhibitor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 Kunitz-type protease inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008200 GCST90248216 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kunitz-type protease inhibitor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 kunitz-type protease inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0801750 GCST90248217 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kv channel-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 kv channel-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801751 GCST90248218 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium/calmodulin-dependent protein kinase type II subunit delta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calcium/calmodulin-dependent protein kinase type II subunit delta measurement http://www.ebi.ac.uk/efo/EFO_0020220 GCST90246827 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium/calmodulin-dependent protein kinase kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 calcium/calmodulin-dependent protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020217 GCST90246828 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathelicidin antimicrobial peptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246829 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calpain-2 catalytic subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calpain-2 catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0801445 GCST90246830 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcineurin subunit B type 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calcineurin subunit B type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020215 GCST90246831 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcineurin subunit B type 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246832 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-dependent phospholipase A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calcium-dependent phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020216 GCST90246833 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Caspase recruitment domain-containing protein 18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246834 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Caspase recruitment domain-containing protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246835 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cardiotrophin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cardiotrophin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020235 GCST90246836 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cocaine- and amphetamine-regulated transcript protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cocaine- and amphetamine-regulated transcript protein measurement http://www.ebi.ac.uk/efo/EFO_0802409 GCST90246837 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein CASC4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein CASC4 measurement http://www.ebi.ac.uk/efo/EFO_0802927 GCST90246838 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Caspase-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 caspase-2 measurement http://www.ebi.ac.uk/efo/EFO_0020240 GCST90246839 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Caspase-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 caspase-3 measurement http://www.ebi.ac.uk/efo/EFO_0008070 GCST90246840 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Caspase-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 caspase-8 measurement http://www.ebi.ac.uk/efo/EFO_0010764 GCST90246841 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Catalase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246842 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90246843 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cathepsin D measurement http://www.ebi.ac.uk/efo/EFO_0010611 GCST90246844 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cathepsin E measurement http://www.ebi.ac.uk/efo/EFO_0020241 GCST90246845 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Catenin alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 catenin alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0802374 GCST90246846 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Catenin beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246847 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cathepsin F measurement http://www.ebi.ac.uk/efo/EFO_0022038 GCST90246848 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cathepsin G measurement http://www.ebi.ac.uk/efo/EFO_0020242 GCST90246849 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90246850 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin K levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246851 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin L2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cathepsin L2 measurement http://www.ebi.ac.uk/efo/EFO_0020244 GCST90246852 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin O levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cathepsin O measurement http://www.ebi.ac.uk/efo/EFO_0802375 GCST90246853 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin S levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90246854 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cathepsin Z levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cathepsin Z measurement http://www.ebi.ac.uk/efo/EFO_0008074 GCST90246855 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Caveolin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 caveolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802376 GCST90246856 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Caveolin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246857 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metalloprotease TIKI1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246858 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 carbonic anhydrase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020227 GCST90246859 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246860 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 carbonic anhydrase 13 measurement http://www.ebi.ac.uk/efo/EFO_0008067 GCST90246861 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 carbonic anhydrase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020228 GCST90246862 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 carbonic anhydrase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020229 GCST90246863 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 carbonic anhydrase 4 measurement http://www.ebi.ac.uk/efo/EFO_0020230 GCST90246864 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 5A, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 carbonic anhydrase 5A, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801450 GCST90246865 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 5B, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246866 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 carbonic anhydrase 6 measurement http://www.ebi.ac.uk/efo/EFO_0008068 GCST90246867 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 carbonic anhydrase 7 measurement http://www.ebi.ac.uk/efo/EFO_0020231 GCST90246868 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 carbonic anhydrase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020232 GCST90246869 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase CBL levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 E3 ubiquitin-protein ligase CBL measurement http://www.ebi.ac.uk/efo/EFO_0801552 GCST90246870 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cerebellin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cerebellin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801466 GCST90246871 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cerebellin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 cerebellin-4 measurement http://www.ebi.ac.uk/efo/EFO_0801467 GCST90246872 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 carboxypeptidase A2 measurement http://www.ebi.ac.uk/efo/EFO_0801451 GCST90246873 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase A4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 carboxypeptidase A4 measurement http://www.ebi.ac.uk/efo/EFO_0801452 GCST90246874 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 carboxypeptidase B measurement http://www.ebi.ac.uk/efo/EFO_0801453 GCST90246875 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 carboxypeptidase B2 measurement http://www.ebi.ac.uk/efo/EFO_0008069 GCST90246876 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidase inhibitor 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peptidase inhibitor 15 measurement http://www.ebi.ac.uk/efo/EFO_0802851 GCST90248993 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 phosphatidylinositol 5-phosphate 4-kinase type-2 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802861 GCST90248994 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol 5-phosphate 4-kinase type-2 beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248995 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 SUMO-protein ligase PIAS3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248996 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polymeric immunoglobulin receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90248997 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PIK3CA/PIK3R1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 PIK3CA/PIK3R1 measurement http://www.ebi.ac.uk/efo/EFO_0021971 GCST90248998 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pikachurin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248999 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Paired immunoglobulin-like type 2 receptor alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 paired immunoglobulin-like type 2 receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0801866 GCST90249000 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PILR alpha-associated neural protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 PILR alpha-associated neural protein measurement http://www.ebi.ac.uk/efo/EFO_0021941 GCST90249001 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein-L-isoaspartate(D-aspartate) O-methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249002 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolactin-inducible protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249003 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol transfer protein alpha isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 phosphatidylinositol transfer protein alpha isoform measurement http://www.ebi.ac.uk/efo/EFO_0802862 GCST90249004 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol transfer protein beta isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 phosphatidylinositol transfer protein beta isoform measurement http://www.ebi.ac.uk/efo/EFO_0802863 GCST90249005 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Activating signal cointegrator 1 complex subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 activating signal cointegrator 1 complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0801340 GCST90246594 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone chaperone ASF1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246595 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Asialoglycoprotein receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 asialoglycoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020164 GCST90246596 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase ASH1L levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histone-lysine N-methyltransferase ASH1L measurement http://www.ebi.ac.uk/efo/EFO_0802603 GCST90246597 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acid-sensing ion channel 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 acid-sensing ion channel 4 measurement http://www.ebi.ac.uk/efo/EFO_0802249 GCST90246598 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Agouti-signaling protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 Agouti-signaling protein measurement http://www.ebi.ac.uk/efo/EFO_0801357 GCST90246599 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sphingomyelin phosphodiesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246600 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acid sphingomyelinase-like phosphodiesterase 3a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90246601 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATPase ASNA1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ATPase ASNA1 measurement http://www.ebi.ac.uk/efo/EFO_0802296 GCST90246602 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aspartyl/asparaginyl beta-hydroxylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 aspartyl/asparaginyl beta-hydroxylase measurement http://www.ebi.ac.uk/efo/EFO_0801396 GCST90246603 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Asporin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 asporin measurement http://www.ebi.ac.uk/efo/EFO_0801397 GCST90246604 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arginine/serine-rich protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 arginine/serine-rich protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802286 GCST90246605 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-synuclein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246606 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Manganese-transporting ATPase 13A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246607 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sarcoplasmic/endoplasmic reticulum calcium ATPase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 sarcoplasmic/endoplasmic reticulum calcium ATPase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802036 GCST90246608 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATPase family AAA domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ATPase family AAA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802297 GCST90246609 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclic AMP-dependent transcription factor ATF-6 alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 cyclic AMP-dependent transcription factor ATF-6 alpha measurement http://www.ebi.ac.uk/efo/EFO_0801505 GCST90246610 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclic AMP-dependent transcription factor ATF-6 beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246611 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADAMTS-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ADAMTS-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802254 GCST90246612 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADAMTS-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246613 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Copper transport protein ATOX1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246614 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP synthase subunit beta, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ATP synthase subunit beta, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020166 GCST90246615 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP synthase subunit f, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246616 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent DNA helicase Q1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ATP-dependent DNA helicase Q1 measurement http://www.ebi.ac.uk/efo/EFO_0802293 GCST90246617 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent RNA helicase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ATP-dependent RNA helicase A measurement http://www.ebi.ac.uk/efo/EFO_0802294 GCST90246618 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Extracellular tyrosine-protein kinase PKDCC levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249018 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pleckstrin homology domain-containing family A member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 pleckstrin homology domain-containing family A member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802873 GCST90249019 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pleckstrin homology domain-containing family A member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249020 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pleckstrin homology domain-containing family A member 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 pleckstrin homology domain-containing family A member 7 measurement http://www.ebi.ac.uk/efo/EFO_0801891 GCST90249021 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyruvate kinase PKLR levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pyruvate kinase PKLR measurement http://www.ebi.ac.uk/efo/EFO_0801982 GCST90249022 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plakophilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249023 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plastin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 plastin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801885 GCST90249024 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plasmin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249025 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plasminogen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249026 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phospholipase B-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 phospholipase B-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0802865 GCST90249027 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 measurement http://www.ebi.ac.uk/efo/EFO_0020108 GCST90249028 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249029 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phospholipase D3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 phospholipase D3 measurement http://www.ebi.ac.uk/efo/EFO_0802866 GCST90249030 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Armadillo repeat-containing protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246582 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Armadillo repeat-containing protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 armadillo repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802288 GCST90246583 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arylsulfatase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90246584 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arylsulfatase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 arylsulfatase B measurement http://www.ebi.ac.uk/efo/EFO_0008030 GCST90246585 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arylsulfatase K levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 arylsulfatase K measurement http://www.ebi.ac.uk/efo/EFO_0801395 GCST90246586 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Agouti-related protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90246587 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ecto-ADP-ribosyltransferase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ecto-ADP-ribosyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801558 GCST90246588 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ecto-ADP-ribosyltransferase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ecto-ADP-ribosyltransferase 4 measurement http://www.ebi.ac.uk/efo/EFO_0801559 GCST90246589 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arylamine N-acetyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 arylamine N-acetyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801394 GCST90246590 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arsenite methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246591 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803306 GCST90246592 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ankyrin repeat and SOCS box protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246593 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prefoldin subunit 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248968 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prefoldin subunit 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248969 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prefoldin subunit 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 prefoldin subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0020652 GCST90248970 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet glycoprotein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 platelet glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008262 GCST90248971 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-glycine alpha-amidating monooxygenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 peptidyl-glycine alpha-amidating monooxygenase measurement http://www.ebi.ac.uk/efo/EFO_0801871 GCST90248972 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostaglandin E synthase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248973 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostaglandin E synthase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248974 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-derived growth factor receptor-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 platelet-derived growth factor receptor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801889 GCST90248975 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein-glutamine gamma-glutamyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248976 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein-glutamine gamma-glutamyltransferase E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein-glutamine gamma-glutamyltransferase e measurement http://www.ebi.ac.uk/efo/EFO_0020690 GCST90248977 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoglycerate kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 phosphoglycerate kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802864 GCST90248978 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet glycoprotein Ib alpha chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 platelet glycoprotein ib alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0020645 GCST90248979 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoglycerate mutase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 phosphoglycerate mutase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020639 GCST90248980 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoglucomutase-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 phosphoglucomutase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021859 GCST90248981 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoglucomutase-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248982 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Progonadoliberin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 progonadoliberin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801924 GCST90248983 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Progonadoliberin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 progonadoliberin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801925 GCST90248984 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidoglycan recognition protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90248985 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidoglycan recognition protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248986 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Procollagen galactosyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 procollagen galactosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801922 GCST90248987 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prorelaxin H2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248988 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostaglandin-H2 D-isomerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 prostaglandin-H2 D-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0801933 GCST90248989 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphate-regulating neutral endopeptidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248990 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PHD finger protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 PHD finger protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802859 GCST90248991 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 14 kDa phosphohistidine phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248992 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pirin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 pirin measurement http://www.ebi.ac.uk/efo/EFO_0801884 GCST90249006 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable inactive ribonuclease-like protein 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 probable inactive ribonuclease-like protein 13 measurement http://www.ebi.ac.uk/efo/EFO_0802906 GCST90249007 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Piwi-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 piwi-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802870 GCST90249008 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform measurement http://www.ebi.ac.uk/efo/EFO_0020637 GCST90249009 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plasma kallikrein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 plasma kallikrein measurement http://www.ebi.ac.uk/efo/EFO_0008260 GCST90249010 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C alpha type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein kinase c alpha type measurement http://www.ebi.ac.uk/efo/EFO_0020677 GCST90249011 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C beta type (splice variant beta-II) levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein kinase c beta type (splice variant beta-II) measurement http://www.ebi.ac.uk/efo/EFO_0020678 GCST90249012 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C gamma type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein kinase c gamma type measurement http://www.ebi.ac.uk/efo/EFO_0020680 GCST90249013 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C iota type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein kinase c iota type measurement http://www.ebi.ac.uk/efo/EFO_0020681 GCST90249014 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C and casein kinase substrate in neurons protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249015 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C and casein kinase substrate in neurons protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249016 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C theta type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein kinase c theta type measurement http://www.ebi.ac.uk/efo/EFO_0020682 GCST90249017 Genome-wide genotyping array 2023-06-28 34197840 Mehrotra R 2021-06-28 Kidney Int www.ncbi.nlm.nih.gov/pubmed/34197840 A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis. Peritoneal solute transfer rates in kidney failure treated with peritoneal dialysis 2,212 European ancestry individuals NA Illumina [7066544] (imputed) 5 response to peritoneal dialysis, peritoneal solute transfer rate http://www.ebi.ac.uk/efo/EFO_0600090, http://www.ebi.ac.uk/efo/EFO_0600089 GCST90058966 Genome-wide genotyping array 2023-06-28 34197840 Mehrotra R 2021-06-28 Kidney Int www.ncbi.nlm.nih.gov/pubmed/34197840 A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis. Peritoneal solute transfer rates in kidney failure treated with peritoneal dialysis 181 Black individuals NA Illumina [NR] (imputed) 0 response to peritoneal dialysis, peritoneal solute transfer rate http://www.ebi.ac.uk/efo/EFO_0600090, http://www.ebi.ac.uk/efo/EFO_0600089 GCST90058967 Genome-wide genotyping array 2023-06-28 34197840 Mehrotra R 2021-06-28 Kidney Int www.ncbi.nlm.nih.gov/pubmed/34197840 A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis. Peritoneal solute transfer rates in kidney failure treated with peritoneal dialysis 109 Asian ancestry individuals NA Illumina [NR] (imputed) 0 response to peritoneal dialysis, peritoneal solute transfer rate http://www.ebi.ac.uk/efo/EFO_0600090, http://www.ebi.ac.uk/efo/EFO_0600089 GCST90058968 Genome-wide genotyping array 2023-06-28 34197840 Mehrotra R 2021-06-28 Kidney Int www.ncbi.nlm.nih.gov/pubmed/34197840 A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis. Peritoneal solute transfer rates in kidney failure treated with peritoneal dialysis 81 European ancestry individuals, 8 Black individuals, 85 Asian ancestry individuals, 29 Native American ancestry individuals, 145 individuals NA Illumina [NR] (imputed) 0 response to peritoneal dialysis, peritoneal solute transfer rate http://www.ebi.ac.uk/efo/EFO_0600090, http://www.ebi.ac.uk/efo/EFO_0600089 GCST90058969 Genome-wide genotyping array 2023-06-28 34197840 Mehrotra R 2021-06-28 Kidney Int www.ncbi.nlm.nih.gov/pubmed/34197840 A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis. Peritoneal solute transfer rates in kidney failure treated with peritoneal dialysis 2,293 European ancestry individuals, 189 Black individuals, 194 Asian ancestry individuals, 29 Native American ancestry individuals, 145 individuals NA Illumina [7066534] (imputed) 7 response to peritoneal dialysis, peritoneal solute transfer rate http://www.ebi.ac.uk/efo/EFO_0600090, http://www.ebi.ac.uk/efo/EFO_0600089 GCST90058970 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plasma protease C1 inhibitor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90249086 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphopantothenoylcysteine decarboxylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 phosphopantothenoylcysteine decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0802867 GCST90249087 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolyl endopeptidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249088 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphopantothenate--cysteine ligase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249089 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein phosphatase inhibitor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249090 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 peptidyl-prolyl cis-trans isomerase B measurement http://www.ebi.ac.uk/efo/EFO_0020626 GCST90249091 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249092 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peptidyl-prolyl cis-trans isomerase D measurement http://www.ebi.ac.uk/efo/EFO_0008256 GCST90249093 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 peptidyl-prolyl cis-trans isomerase E measurement http://www.ebi.ac.uk/efo/EFO_0008257 GCST90249094 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptidyl-prolyl cis-trans isomerase F, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 peptidyl-prolyl cis-trans isomerase F, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020627 GCST90249095 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proline-serine-threonine phosphatase-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249096 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein phosphatase 1 regulatory subunit 3B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein phosphatase 1 regulatory subunit 3B measurement http://www.ebi.ac.uk/efo/EFO_0802956 GCST90249097 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoribosyl pyrophosphate synthase-associated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 phosphoribosyl pyrophosphate synthase-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802868 GCST90249098 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoribosyl pyrophosphate synthase-associated protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249099 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Palmitoyl-protein thioesterase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 palmitoyl-protein thioesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801867 GCST90249100 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein quaking levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249101 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PRA1 family protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249102 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PR domain zinc finger protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 PR domain zinc finger protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801904 GCST90249103 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PR domain zinc finger protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 PR domain zinc finger protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802893 GCST90249104 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteoglycan 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 proteoglycan 3 measurement http://www.ebi.ac.uk/efo/EFO_0802970 GCST90249105 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxisome proliferator-activated receptor gamma coactivator 1-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249106 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Major prion protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 major prion protein measurement http://www.ebi.ac.uk/efo/EFO_0802725 GCST90249107 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase parkin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 e3 ubiquitin-protein ligase parkin measurement http://www.ebi.ac.uk/efo/EFO_0802506 GCST90249108 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prion-like protein doppel levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249109 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prokineticin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 prokineticin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020655 GCST90249110 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prokineticin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249111 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Promotilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 promotilin measurement http://www.ebi.ac.uk/efo/EFO_0801930 GCST90249112 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pro-opiomelanocortin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249113 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolactin receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 prolactin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020656 GCST90249114 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Properdin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 properdin measurement http://www.ebi.ac.uk/efo/EFO_0008269 GCST90249115 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ProSAAS levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249116 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prosaposin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249117 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostasin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249118 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein 4.1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249119 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prothrombin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 prothrombin measurement http://www.ebi.ac.uk/efo/EFO_0020692 GCST90249120 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protrudin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protrudin measurement http://www.ebi.ac.uk/efo/EFO_0802976 GCST90249121 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 measurement http://www.ebi.ac.uk/efo/EFO_0801905 GCST90249122 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proline-rich protein 27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249123 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pre-mRNA-processing factor 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 pre-mRNA-processing factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0802894 GCST90249124 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolactin-releasing peptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 prolactin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0802915 GCST90249125 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein shisa-2 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249126 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostate-specific antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 prostate-specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0020660 GCST90249127 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit alpha type-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 proteasome subunit alpha type-1 measurement http://www.ebi.ac.uk/efo/EFO_0020663 GCST90249128 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit alpha type-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 proteasome subunit alpha type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020664 GCST90249129 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit alpha type-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249130 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit alpha type-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 proteasome subunit alpha type-4 measurement http://www.ebi.ac.uk/efo/EFO_0802922 GCST90249131 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit alpha type-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249132 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit alpha type-6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 proteasome subunit alpha type-6 measurement http://www.ebi.ac.uk/efo/EFO_0020665 GCST90249133 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit alpha type-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249134 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit beta type-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249135 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (anti-SARS-CoV-2 Spike antibody levels at two months after first dose) 873 Italian ancestry individuals NA Illumina [4989554] (imputed) 10 SARS-CoV-2 antibody measurement, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803360, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90256681 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (anti-SARS-CoV-2 Spike antibody levels at four months after first dose) 868 Italian ancestry individuals NA Illumina [4989554] (imputed) 10 SARS-CoV-2 antibody measurement, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803360, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90256682 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (percentage decrease of anti-SARS-CoV-2 Spike antibody levels from two to four months after first dose) 868 Italian ancestry individuals NA Illumina [4989554] (imputed) 10 SARS-CoV-2 antibody measurement, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803360, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90256683 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (asthenia) 386 Italian ancestry cases, 487 Italian ancestry controls NA Illumina [4989554] (imputed) 0 asthenia, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0007625, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90256684 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (joint pain) 320 Italian ancestry cases, 553 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine, Arthralgia http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0002829 GCST90256685 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (chills) 233 Italian ancestry cases, 640 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803362 GCST90256686 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (diarrhea) 39 Italian ancestry cases, 834 Italian ancestry controls NA Illumina [4985724] (imputed) 0 response to COVID-19 vaccine, Diarrhea http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0002014 GCST90256687 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (fatigues) 538 Italian ancestry cases, 335 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine, Fatigue http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0012378 GCST90256688 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (fever) 169 Italian ancestry cases, 704 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine, Fever http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0001945 GCST90256689 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (headache) 241 Italian ancestry cases, 632 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine, Headache http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0002315 GCST90256690 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (lymphadenopathy) 61 Italian ancestry cases, 812 Italian ancestry controls NA Illumina [4989346] (imputed) 1 response to COVID-19 vaccine, Lymphadenopathy http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0002716 GCST90256691 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (myalgia) 266 Italian ancestry cases, 607 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine, Myalgia http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0003326 GCST90256692 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (nausea) 87 Italian ancestry cases, 786 Italian ancestry controls NA Illumina [4989553] (imputed) 0 response to COVID-19 vaccine, Nausea http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0002018 GCST90256693 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (pain at injection site) 703 Italian ancestry cases, 170 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine, pain http://www.ebi.ac.uk/efo/EFO_0803362, http://www.ebi.ac.uk/efo/EFO_0003843 GCST90256694 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (rush) 14 Italian ancestry cases, 859 Italian ancestry controls NA Illumina [4844682] (imputed) 0 response to COVID-19 vaccine, Purpura http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0000979 GCST90256695 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (swelling) 117 Italian ancestry cases, 756 Italian ancestry controls NA Illumina [4989554] (imputed) 0 response to COVID-19 vaccine, localized superficial swelling, mass, or lump http://www.ebi.ac.uk/efo/EFO_0803362, http://www.ebi.ac.uk/efo/EFO_0010683 GCST90256696 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (tachycardia) 31 Italian ancestry cases, 842 Italian ancestry controls NA Illumina [4976919] (imputed) 0 response to COVID-19 vaccine, Tachycardia http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0001649 GCST90256697 Genome-wide genotyping array 2023-08-03 37469131 Magri C 2023-07-19 HLA www.ncbi.nlm.nih.gov/pubmed/37469131 Genome-wide association studies of response and side effects to the BNT162b2 vaccine in Italian healthcare workers: Increased antibody levels and side effects in carriers of the HLA-A*03:01 allele. Response to BNT162b2 vaccine (vomiting) 15 Italian ancestry cases, 858 Italian ancestry controls NA Illumina [4868696] (imputed) 0 response to COVID-19 vaccine, Vomiting http://www.ebi.ac.uk/efo/EFO_0803362, http://purl.obolibrary.org/obo/HP_0002013 GCST90256698 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Golgi SNAP receptor complex member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 Golgi SNAP receptor complex member 1 measurement http://www.ebi.ac.uk/efo/EFO_0801651 GCST90247781 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Golgi SNAP receptor complex member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247782 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable G-protein coupled receptor 101 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 probable G-protein coupled receptor 101 measurement http://www.ebi.ac.uk/efo/EFO_0802905 GCST90247783 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein GPR107 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein GPR107 measurement http://www.ebi.ac.uk/efo/EFO_0802946 GCST90247784 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adhesion G-protein coupled receptor G5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 adhesion G-protein coupled receptor G5 measurement http://www.ebi.ac.uk/efo/EFO_0021980 GCST90247785 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adhesion G protein-coupled receptor F5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 adhesion G protein-coupled receptor F5 measurement http://www.ebi.ac.uk/efo/EFO_0801346 GCST90247786 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable G-protein coupled receptor 135 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 probable G-protein coupled receptor 135 measurement http://www.ebi.ac.uk/efo/EFO_0801916 GCST90247787 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycerophosphocholine phosphodiesterase GPCPD1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glycerophosphocholine phosphodiesterase GPCPD1 measurement http://www.ebi.ac.uk/efo/EFO_0802574 GCST90247788 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutaminyl-peptide cyclotransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 glutaminyl-peptide cyclotransferase measurement http://www.ebi.ac.uk/efo/EFO_0802570 GCST90247789 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutaminyl-peptide cyclotransferase-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glutaminyl-peptide cyclotransferase-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801632 GCST90247790 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycoprotein hormone alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glycoprotein hormone alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0801645 GCST90247791 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GPN-loop GTPase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247792 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adhesion G-protein coupled receptor F1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 adhesion G-protein coupled receptor F1 measurement http://www.ebi.ac.uk/efo/EFO_0801347 GCST90247793 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. G-protein coupled receptor 26 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 g-protein coupled receptor 26 measurement http://www.ebi.ac.uk/efo/EFO_0802558 GCST90247794 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adhesion G-protein coupled receptor G1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247795 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet glycoprotein V levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 platelet glycoprotein V measurement http://www.ebi.ac.uk/efo/EFO_0802872 GCST90247796 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet glycoprotein VI levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 platelet glycoprotein VI measurement http://www.ebi.ac.uk/efo/EFO_0008263 GCST90247797 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione peroxidase 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glutathione peroxidase 7 measurement http://www.ebi.ac.uk/efo/EFO_0801635 GCST90247798 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutamate receptor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glutamate receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0801630 GCST90247799 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Grancalcin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 grancalcin measurement http://www.ebi.ac.uk/efo/EFO_0801653 GCST90247800 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granulins levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90247801 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granulysin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90247802 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granzyme A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90247803 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granzyme B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 granzyme b measurement http://www.ebi.ac.uk/efo/EFO_0020418 GCST90247804 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granzyme K levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 granzyme K measurement http://www.ebi.ac.uk/efo/EFO_0801654 GCST90247805 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glypican-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 glypican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020414 GCST90247756 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glypican-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glypican-3 measurement http://www.ebi.ac.uk/efo/EFO_0020415 GCST90247757 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glypican-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247758 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glypican-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 glypican-5 measurement http://www.ebi.ac.uk/efo/EFO_0008139 GCST90247759 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glypican-6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glypican-6 measurement http://www.ebi.ac.uk/efo/EFO_0021871 GCST90247760 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycoprotein hormones alpha chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glycoprotein hormones alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0802577 GCST90247761 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycosyltransferase-like protein LARGE1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glycosyltransferase-like protein LARGE1 measurement http://www.ebi.ac.uk/efo/EFO_0802578 GCST90247762 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycine N-acyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247763 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycine N-methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247764 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycylpeptide N-tetradecanoyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glycylpeptide n-tetradecanoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020413 GCST90247765 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycylpeptide N-tetradecanoyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247766 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycogen phosphorylase, liver form levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glycogen phosphorylase, liver form measurement http://www.ebi.ac.uk/efo/EFO_0801642 GCST90247767 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycoprotein Xg levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glycoprotein Xg measurement http://www.ebi.ac.uk/efo/EFO_0801646 GCST90247768 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glyoxylate reductase/hydroxypyruvate reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247769 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granulocyte-macrophage colony-stimulating factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 granulocyte-macrophage colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0020417 GCST90247770 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granulocyte-macrophage colony-stimulating factor receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 granulocyte-macrophage colony-stimulating factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0802579 GCST90247771 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GMP reductase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247772 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GMP reductase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247773 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GMP synthase [glutamine-hydrolyzing] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247774 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanine nucleotide-binding protein G(k) subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 guanine nucleotide-binding protein G(k) subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801661 GCST90247775 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucosamine-6-phosphate isomerase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glucosamine-6-phosphate isomerase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801627 GCST90247776 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTPase NRas levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247777 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-soluble NSF attachment protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247778 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Golgin subfamily A member 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247779 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Golgi membrane protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 Golgi membrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801650 GCST90247780 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related and estrogen-regulated growth inhibitor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249283 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Resistin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90249284 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoic acid early transcript 1G protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249285 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoblastoma-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 retinoblastoma-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0020706 GCST90249286 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanine nucleotide exchange factor MSS4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247833 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanylyl cyclase-activating protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 guanylyl cyclase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801663 GCST90247834 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanylate kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247835 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanine nucleotide exchange factor VAV3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 guanine nucleotide exchange factor VAV3 measurement http://www.ebi.ac.uk/efo/EFO_0802587 GCST90247836 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanylate cyclase activator 2B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 guanylate cyclase activator 2B measurement http://www.ebi.ac.uk/efo/EFO_0802589 GCST90247837 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Group XIIB secretory phospholipase A2-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 group XIIB secretory phospholipase A2-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801657 GCST90247838 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucoside xylosyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glucoside xylosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801629 GCST90247839 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone H2A type 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histone H2A type 3 measurement http://www.ebi.ac.uk/efo/EFO_0021953 GCST90247840 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone H2B type 2-E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histone H2B type 2-E measurement http://www.ebi.ac.uk/efo/EFO_0021952 GCST90247841 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone H2B type 3-B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247842 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High affinity immunoglobulin alpha and immunoglobulin mu Fc receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 high affinity immunoglobulin alpha and immunoglobulin mu Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0802598 GCST90247843 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High affinity immunoglobulin epsilon receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247844 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High affinity immunoglobulin gamma Fc receptor I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 high affinity immunoglobulin gamma fc receptor i measurement http://www.ebi.ac.uk/efo/EFO_0020447 GCST90247845 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High affinity nerve growth factor receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 high affinity nerve growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020448 GCST90247846 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 28 kDa heat- and acid-stable phosphoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247847 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Harmonin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247848 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hemoglobin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90247849 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hemoglobin subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247850 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hemoglobin subunit delta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247851 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparin-binding EGF-like growth factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 heparin-binding egf-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020438 GCST90247852 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hemoglobin subunit theta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 hemoglobin subunit theta-1 measurement http://www.ebi.ac.uk/efo/EFO_0801669 GCST90247853 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hemoglobin subunit zeta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 hemoglobin subunit zeta measurement http://www.ebi.ac.uk/efo/EFO_0801670 GCST90247854 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparin cofactor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247855 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Human Chorionic Gonadotropin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90247856 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone deacetylase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247857 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone deacetylase 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 histone deacetylase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020453 GCST90247858 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatoma-derived growth factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247859 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatoma-derived growth factor-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247860 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatoma-derived growth factor-related protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247861 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Haloacid dehalogenase-like hydrolase domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 haloacid dehalogenase-like hydrolase domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801664 GCST90247862 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Haloacid dehalogenase-like hydrolase domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247863 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heme-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247864 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase HECW1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 E3 ubiquitin-protein ligase HECW1 measurement http://www.ebi.ac.uk/efo/EFO_0802505 GCST90247865 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hemojuvelin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 hemojuvelin measurement http://www.ebi.ac.uk/efo/EFO_0008148 GCST90247866 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. HEPACAM family member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 HEPACAM family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802591 GCST90247867 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatitis A virus cellular receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 hepatitis A virus cellular receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010601 GCST90247868 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatitis A virus cellular receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90247869 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable E3 ubiquitin-protein ligase HERC4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 probable E3 ubiquitin-protein ligase HERC4 measurement http://www.ebi.ac.uk/efo/EFO_0802903 GCST90247870 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ISG15--protein ligase HERC5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 E3 ISG15--protein ligase HERC5 measurement http://www.ebi.ac.uk/efo/EFO_0802501 GCST90247871 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein HEXIM1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247872 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein HEXIM2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247873 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homogentisate 1,2-dioxygenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 homogentisate 1,2-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0802609 GCST90247874 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatocyte growth factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90247875 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatocyte growth factor activator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 hepatocyte growth factor activator measurement http://www.ebi.ac.uk/efo/EFO_0008152 GCST90247876 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatocyte growth factor-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90247877 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Replication initiator 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 replication initiator 1 measurement http://www.ebi.ac.uk/efo/EFO_0802001 GCST90249282 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Roundabout homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 roundabout homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0803039 GCST90249355 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Roundabout homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 roundabout homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0020713 GCST90249356 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Roundabout homolog 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 roundabout homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0020714 GCST90249357 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho-associated protein kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 rho-associated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0803021 GCST90249358 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive tyrosine-protein kinase transmembrane receptor ROR1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249359 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Replication protein A 32 kDa subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249360 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-directed RNA polymerases I, II, and III subunit RPABC4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249361 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-directed RNA polymerases I and III subunit RPAC1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 DNA-directed RNA polymerases I and III subunit RPAC1 measurement http://www.ebi.ac.uk/efo/EFO_0801535 GCST90249362 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-directed RNA polymerase II subunit RPB11-a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249363 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-directed RNA polymerase III subunit RPC6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249364 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-directed RNA polymerase III subunit RPC9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249365 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribulose-phosphate 3-epimerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ribulose-phosphate 3-epimerase measurement http://www.ebi.ac.uk/efo/EFO_0802025 GCST90249366 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rap guanine nucleotide exchange factor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 rap guanine nucleotide exchange factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0802989 GCST90249367 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribose-5-phosphate isomerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249368 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA polymerase II elongation factor ELL levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 RNA polymerase II elongation factor ELL measurement http://www.ebi.ac.uk/efo/EFO_0802028 GCST90249369 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA polymerase II elongation factor ELL2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RNA polymerase II elongation factor ELL2 measurement http://www.ebi.ac.uk/efo/EFO_0803035 GCST90249370 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RAF proto-oncogene serine/threonine-protein kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249371 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonuclease P protein subunit p30 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249372 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulation of nuclear pre-mRNA domain-containing protein 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 regulation of nuclear pre-mRNA domain-containing protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0801994 GCST90249373 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulation of nuclear pre-mRNA domain-containing protein 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249374 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related GTP-binding protein C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249375 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein R-Ras levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249376 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras-related protein R-Ras2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249377 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribosome-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ribosome-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803026 GCST90249378 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Exosome complex component RRP40 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 exosome complex component RRP40 measurement http://www.ebi.ac.uk/efo/EFO_0801594 GCST90249379 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 39S ribosomal protein L2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249330 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 39S ribosomal protein L21, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249331 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 39S ribosomal protein L32, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249332 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 39S ribosomal protein L33, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 39S ribosomal protein L33, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801332 GCST90249333 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 39S ribosomal protein L55, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249334 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of microtubule dynamics protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 regulator of microtubule dynamics protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801998 GCST90249335 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RecQ-mediated genome instability protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 recQ-mediated genome instability protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801992 GCST90249336 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF114 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 E3 ubiquitin-protein ligase RNF114 measurement http://www.ebi.ac.uk/efo/EFO_0802510 GCST90249337 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RING finger protein 122 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 RING finger protein 122 measurement http://www.ebi.ac.uk/efo/EFO_0803028 GCST90249338 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF128 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 E3 ubiquitin-protein ligase RNF128 measurement http://www.ebi.ac.uk/efo/EFO_0801555 GCST90249339 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF146 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249340 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF149 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 E3 ubiquitin-protein ligase RNF149 measurement http://www.ebi.ac.uk/efo/EFO_0802511 GCST90249341 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RING finger protein 150 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RING finger protein 150 measurement http://www.ebi.ac.uk/efo/EFO_0803030 GCST90249342 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RING finger protein 215 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RING finger protein 215 measurement http://www.ebi.ac.uk/efo/EFO_0803031 GCST90249343 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonuclease 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ribonuclease 4 measurement http://www.ebi.ac.uk/efo/EFO_0802017 GCST90249344 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonuclease K6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ribonuclease K6 measurement http://www.ebi.ac.uk/efo/EFO_0802018 GCST90249345 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonuclease H1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ribonuclease H1 measurement http://www.ebi.ac.uk/efo/EFO_0022020 GCST90249346 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho-related GTP-binding protein RhoE levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249347 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 E3 ubiquitin-protein ligase RNF13 measurement http://www.ebi.ac.uk/efo/EFO_0801556 GCST90249348 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RING finger protein 24 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249349 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF34 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 E3 ubiquitin-protein ligase RNF34 measurement http://www.ebi.ac.uk/efo/EFO_0802512 GCST90249350 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF43 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 e3 ubiquitin-protein ligase RNF43 measurement http://www.ebi.ac.uk/efo/EFO_0021886 GCST90249351 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase RNF8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 E3 ubiquitin-protein ligase RNF8 measurement http://www.ebi.ac.uk/efo/EFO_0801557 GCST90249352 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonuclease pancreatic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ribonuclease pancreatic measurement http://www.ebi.ac.uk/efo/EFO_0802019 GCST90249353 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonuclease T2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249354 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Insulin area under the curve) 730 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12198141] (imputed) 0 insulin measurement, response to metformin http://www.ebi.ac.uk/efo/EFO_0004467, http://purl.obolibrary.org/obo/GO_1901558 GCST90269867 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Fasting glucose levels adjusted for baseline glucose levels) 807 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12657451] (imputed) 3 fasting blood glucose measurement, response to metformin http://www.ebi.ac.uk/efo/EFO_0004465, http://purl.obolibrary.org/obo/GO_1901558 GCST90269868 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Glucose levels at 120 minutes adjusted for baseline glucose levels) 790 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12521399] (imputed) 0 response to metformin, glucose tolerance test http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269869 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Glucose levels at 30 minutes adjusted for baseline glucose levels) 789 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12540911] (imputed) 0 response to metformin, glucose tolerance test http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269870 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Glucose levels at 60 minutes adjusted for baseline glucose levels) 794 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12547822] (imputed) 1 response to metformin, glucose tolerance test http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269871 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Fasting glucose 851 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12901357] (imputed) 1 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90269872 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Glucose levels at 120 minutes adjusted for baseline glucose levels) 643 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [11326460] (imputed) 0 response to sulfonylurea, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269873 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Glucose levels at 180 minutes adjusted for baseline glucose levels) 568 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10887848] (imputed) 0 response to sulfonylurea, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269874 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Glucose levels at 240 minutes adjusted for baseline glucose levels) 546 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10708292] (imputed) 0 response to sulfonylurea, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269875 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Glucose levels at 30 minutes adjusted for baseline glucose levels) 832 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12722186] (imputed) 0 response to sulfonylurea, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269876 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Glucose levels at 60 minutes adjusted for baseline glucose levels) 830 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12705251] (imputed) 1 response to sulfonylurea, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269877 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Glucose levels at 90 minutes adjusted for baseline glucose levels) 743 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12023140] (imputed) 0 response to sulfonylurea, glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269878 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Change in fasting glucose levels adjusted for baseline glucose levels) 805 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12653767] (imputed) 0 fasting blood glucose change measurement, response to metformin http://www.ebi.ac.uk/efo/EFO_0010120, http://purl.obolibrary.org/obo/GO_1901558 GCST90269879 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Change in fasting insulin levels adjusted for baseline insulin levels) 778 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12453441] (imputed) 0 response to metformin, fasting blood insulin measurement http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004466 GCST90269880 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Slope to glucose trough adjusted for baseline glucose levels) 549 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10773724] (imputed) 0 response to sulfonylurea, glucose change measurement http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0020881 GCST90269881 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Slope to glucose recovery adjusted for baseline glucose levels) 464 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [9989986] (imputed) 0 response to sulfonylurea, glucose change measurement http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0020881 GCST90269882 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Fasting insulin levels) 776 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12516558] (imputed) 0 response to metformin, fasting blood insulin measurement http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004466 GCST90269883 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Insulin levels at 120 minutes) 774 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12443117] (imputed) 0 response to metformin, glucose tolerance test http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269884 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Insulin levels at 30 minutes) 769 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12447720] (imputed) 0 response to metformin, glucose tolerance test http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269885 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Insulin levels at 60 minutes) 776 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12483998] (imputed) 1 response to metformin, glucose tolerance test http://purl.obolibrary.org/obo/GO_1901558, http://www.ebi.ac.uk/efo/EFO_0004307 GCST90269886 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Fasting insulin 828 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12708558] (imputed) 0 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST90269887 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Insulin levels at 120 minutes) 627 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [11223850] (imputed) 0 insulin metabolic clearance rate measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0006830, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269888 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Insulin levels at 180 minutes) 556 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10768148] (imputed) 0 insulin metabolic clearance rate measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0006830, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269889 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Insulin levels at 240 minutes) 535 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10560048] (imputed) 0 insulin metabolic clearance rate measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0006830, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269890 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Insulin levels at 30 minutes) 807 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12534687] (imputed) 1 insulin metabolic clearance rate measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0006830, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269891 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Insulin levels at 60 minutes) 808 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12551193] (imputed) 0 insulin metabolic clearance rate measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0006830, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269892 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Insulin levels at 90 minutes) 728 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [11945771] (imputed) 0 insulin metabolic clearance rate measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0006830, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269893 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Peak insulin levels adjusted for baseline insulin levels) 531 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10540859] (imputed) 0 insulin measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0004467, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269894 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Change in HOMA B) 760 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12371656] (imputed) 0 HOMA-B, response to metformin http://www.ebi.ac.uk/efo/EFO_0004469, http://purl.obolibrary.org/obo/GO_1901558 GCST90269895 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to metfomin (Change in HOMA IR) 796 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [12600931] (imputed) 0 HOMA-IR, response to metformin http://www.ebi.ac.uk/efo/EFO_0004501, http://purl.obolibrary.org/obo/GO_1901558 GCST90269896 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Glucose trough adjusted for baseline glucose) 550 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10786001] (imputed) 0 glucose measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0004468, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269897 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Time to peak insulin) 550 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10786001] (imputed) 0 peak insulin response measurement, response to sulfonylurea http://www.ebi.ac.uk/efo/EFO_0008000, http://www.ebi.ac.uk/efo/EFO_0007922 GCST90269898 Genome-wide genotyping array 2023-05-31 37233759 Li JH 2023-05-26 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37233759 Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH. Response to glipizide (Time to glucose trough) 550 Black, European, Hispanic, Asian or unknown ancestry individuals at risk of type 2 diabetes NA Illumina [10786001] (imputed) 2 response to sulfonylurea, glucose change measurement http://www.ebi.ac.uk/efo/EFO_0007922, http://www.ebi.ac.uk/efo/EFO_0020881 GCST90269899 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone deacetylase complex subunit SAP30 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histone deacetylase complex subunit SAP30 measurement http://www.ebi.ac.uk/efo/EFO_0802601 GCST90249428 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proactivator polypeptide-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 proactivator polypeptide-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801912 GCST90249429 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-binding protein SATB1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DNA-binding protein SATB1 measurement http://www.ebi.ac.uk/efo/EFO_0802483 GCST90249430 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-binding protein SATB2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 DNA-binding protein SATB2 measurement http://www.ebi.ac.uk/efo/EFO_0802484 GCST90249431 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribosome maturation protein SBDS levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ribosome maturation protein sbds measurement http://www.ebi.ac.uk/efo/EFO_0020711 GCST90249432 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein transport protein Sec61 subunit gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein transport protein Sec61 subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0802965 GCST90249433 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Short-chain specific acyl-CoA dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249434 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secretory carrier-associated membrane protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 secretory carrier-associated membrane protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803049 GCST90249435 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Soluble calcium-activated nucleotidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 soluble calcium-activated nucleotidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803089 GCST90249436 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Scavenger receptor class A member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 scavenger receptor class A member 3 measurement http://www.ebi.ac.uk/efo/EFO_0803044 GCST90249437 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Scavenger receptor class A member 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 scavenger receptor class A member 5 measurement http://www.ebi.ac.uk/efo/EFO_0802037 GCST90249438 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small conductance calcium-activated potassium channel protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 small conductance calcium-activated potassium channel protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803081 GCST90249439 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Monocyte differentiation antigen CD14, soluble levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249440 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium- and chloride-dependent glycine transporter 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sodium- and chloride-dependent glycine transporter 1 measurement http://www.ebi.ac.uk/efo/EFO_0803086 GCST90249441 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium- and chloride-dependent neutral and basic amino acid transporter B(0+) levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 sodium- and chloride-dependent neutral and basic amino acid transporter B(0+) measurement http://www.ebi.ac.uk/efo/EFO_0803304 GCST90249442 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SUMO-conjugating enzyme UBC9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sumo-conjugating enzyme UBC9 measurement http://www.ebi.ac.uk/efo/EFO_0020757 GCST90249443 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Scavenger receptor class F member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90249444 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Scavenger receptor class F member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90249445 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secretogranin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 secretogranin-1 measurement http://www.ebi.ac.uk/efo/EFO_0803047 GCST90249446 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secretogranin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 secretogranin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802042 GCST90249447 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stem Cell Growth Factor-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 stem cell growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020754 GCST90249448 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stem Cell Growth Factor-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 stem Cell Growth Factor-beta measurement http://www.ebi.ac.uk/efo/EFO_0802090 GCST90249449 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Scavenger receptor cysteine-rich type 1 protein M130 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 scavenger receptor cysteine-rich type 1 protein m130 measurement http://www.ebi.ac.uk/efo/EFO_0020717 GCST90249450 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytokine SCM-1 beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249451 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polycomb protein SCMH1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 polycomb protein SCMH1 measurement http://www.ebi.ac.uk/efo/EFO_0801898 GCST90249452 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium-coupled monocarboxylate transporter 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 12 sodium-coupled monocarboxylate transporter 1 measurement http://www.ebi.ac.uk/efo/EFO_0802076 GCST90249453 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium channel subunit beta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sodium channel subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0803085 GCST90249454 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium channel subunit beta-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249455 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein SCO1 homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein SCO1 homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802962 GCST90249456 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein SCO2 homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249457 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SCP2 sterol-binding domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 SCP2 sterol-binding domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802038 GCST90249458 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal peptide, CUB and EGF-like domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 signal peptide, CUB and EGF-like domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803074 GCST90249459 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal peptide, CUB and EGF-like domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249460 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syndecan-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249461 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntenin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249462 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntenin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249463 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Spliceosome RNA helicase DDX39B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 spliceosome RNA helicase DDX39B measurement http://www.ebi.ac.uk/efo/EFO_0802084 GCST90249464 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stromal cell-derived factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 stromal cell-derived factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020756 GCST90249465 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stromal cell-derived factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249466 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stromal cell-derived factor 2-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 stromal cell-derived factor 2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803105 GCST90249467 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorbitol dehydrogenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249468 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Superoxide dismutase [Mn], mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249469 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sin3 histone deacetylase corepressor complex component SDS3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249470 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine dehydratase-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249471 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein sel-1 homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein sel-1 homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0801962 GCST90249472 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Seizure 6-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249473 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Seizure 6-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 seizure 6-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020720 GCST90249474 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein SEC13 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein SEC13 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801961 GCST90249475 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secretagogin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 secretagogin measurement http://www.ebi.ac.uk/efo/EFO_0803045 GCST90249476 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secretin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 secretin measurement http://www.ebi.ac.uk/efo/EFO_0020719 GCST90249477 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Junctophilin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 junctophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802667 GCST90248147 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Junctophilin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 junctophilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802668 GCST90248148 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Junctophilin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248149 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein JTB levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein JTB measurement http://www.ebi.ac.uk/efo/EFO_0802948 GCST90248150 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Jumonji levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248151 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kidney-associated antigen 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248152 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenylate kinase 4, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248153 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallistatin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90248154 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248155 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. kallikrein-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90248156 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 kallikrein-12 measurement http://www.ebi.ac.uk/efo/EFO_0008194 GCST90248157 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 kallikrein-13 measurement http://www.ebi.ac.uk/efo/EFO_0020512 GCST90248158 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90248159 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 kallikrein-15 measurement http://www.ebi.ac.uk/efo/EFO_0802669 GCST90248160 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90248161 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 kallikrein-6 measurement http://www.ebi.ac.uk/efo/EFO_0801739 GCST90248162 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 kallikrein-7 measurement http://www.ebi.ac.uk/efo/EFO_0008195 GCST90248163 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kallikrein-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90248164 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase kappa 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glutathione S-transferase kappa 1 measurement http://www.ebi.ac.uk/efo/EFO_0802571 GCST90248165 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kazal-type serine protease inhibitor domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248166 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 2DL1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248167 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 2DL2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 killer cell immunoglobulin-like receptor 2DL2 measurement http://www.ebi.ac.uk/efo/EFO_0801744 GCST90248168 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 2DL3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248169 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 2DL4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90248170 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 2DL5A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 killer cell immunoglobulin-like receptor 2DL5A measurement http://www.ebi.ac.uk/efo/EFO_0801745 GCST90248171 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90249551 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sialic acid-binding Ig-like lectin 8 measurement http://www.ebi.ac.uk/efo/EFO_0802067 GCST90249552 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 sialic acid-binding Ig-like lectin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008286 GCST90249553 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Single Ig IL-1-related receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 single Ig IL-1-related receptor measurement http://www.ebi.ac.uk/efo/EFO_0802072 GCST90249554 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small integral membrane protein 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249555 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small integral membrane protein 24 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249556 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small integral membrane protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 small integral membrane protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0802075 GCST90249557 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stress-induced-phosphoprotein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 stress-induced-phosphoprotein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020755 GCST90249558 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal-regulatory protein beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 signal-regulatory protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0802069 GCST90249559 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal-regulatory protein gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 signal-regulatory protein gamma measurement http://www.ebi.ac.uk/efo/EFO_0802071 GCST90249560 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium-independent sulfate anion transporter levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sodium-independent sulfate anion transporter measurement http://www.ebi.ac.uk/efo/EFO_0803087 GCST90249561 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. S-phase kinase-associated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 s-phase kinase-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020715 GCST90249562 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signaling lymphocytic activation molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 signaling lymphocytic activation molecule measurement http://www.ebi.ac.uk/efo/EFO_0803076 GCST90249563 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SLAM family member 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 SLAM family member 6 measurement http://www.ebi.ac.uk/efo/EFO_0020742 GCST90249564 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SLAM family member 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90249565 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SLAM family member 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 SLAM family member 8 measurement http://www.ebi.ac.uk/efo/EFO_0803079 GCST90249566 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SLIT and NTRK-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 SLIT and NTRK-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802074 GCST90249567 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SLIT and NTRK-like protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 SLIT and NTRK-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803080 GCST90249568 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SLIT and NTRK-like protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 slit and ntrk-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020743 GCST90249569 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SLIT and NTRK-like protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249570 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Somatoliberin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249571 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Slit homolog 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249572 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Slit homolog 2 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249573 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Slit homolog 3 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249574 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SAFB-like transcription modulator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249575 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kinesin-like protein KIF3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248197 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA/RNA-binding protein KIN17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DNA/RNA-binding protein KIN17 measurement http://www.ebi.ac.uk/efo/EFO_0801536 GCST90248198 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kininogen-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248199 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kininostatin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248200 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kish-A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein kish-A measurement http://www.ebi.ac.uk/efo/EFO_0802950 GCST90248201 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kish-B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein kish-B measurement http://www.ebi.ac.uk/efo/EFO_0802951 GCST90248202 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metastasis-suppressor KiSS-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248203 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kit ligand levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 kit ligand measurement http://www.ebi.ac.uk/efo/EFO_0010612 GCST90248204 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kinesin light chain 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248205 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kelch-like protein 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 kelch-like protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0802670 GCST90248206 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kelch-like protein 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 kelch-like protein 13 measurement http://www.ebi.ac.uk/efo/EFO_0801741 GCST90248207 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Klotho levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248208 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell lectin-like receptor subfamily B member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248209 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell lectin-like receptor subfamily G member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248210 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kremen protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 kremen protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801749 GCST90248211 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribosomal protein S6 kinase alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248212 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribosomal protein S6 kinase beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248213 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialoadhesin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sialoadhesin measurement http://www.ebi.ac.uk/efo/EFO_0020740 GCST90249543 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249544 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sialic acid-binding Ig-like lectin 11 measurement http://www.ebi.ac.uk/efo/EFO_0802065 GCST90249545 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 sialic acid-binding Ig-like lectin 12 measurement http://www.ebi.ac.uk/efo/EFO_0802066 GCST90249546 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90249547 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249548 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 15 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249549 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialic acid-binding Ig-like lectin 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sialic acid-binding Ig-like lectin 6 measurement http://www.ebi.ac.uk/efo/EFO_0008285 GCST90249550 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 2DS2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 killer cell immunoglobulin-like receptor 2DS2 measurement http://www.ebi.ac.uk/efo/EFO_0801746 GCST90248172 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 2DS4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248173 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 3DL1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248174 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 3DL2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 killer cell immunoglobulin-like receptor 3DL2 measurement http://www.ebi.ac.uk/efo/EFO_0020518 GCST90248175 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Killer cell immunoglobulin-like receptor 3DS1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 killer cell immunoglobulin-like receptor 3DS1 measurement http://www.ebi.ac.uk/efo/EFO_0020519 GCST90248176 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BTB/POZ domain-containing protein KCTD5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 BTB/POZ domain-containing protein KCTD5 measurement http://www.ebi.ac.uk/efo/EFO_0802340 GCST90248177 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. KDEL motif-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248178 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. KDEL motif-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 KDEL motif-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801740 GCST90248179 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-ketodihydrosphingosine reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248180 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kelch-like ECH-associated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 kelch-like ECH-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0022023 GCST90248181 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kell blood group glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 kell blood group glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0802671 GCST90248182 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratocan levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248183 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratin, type I cytoskeletal 17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 keratin, type I cytoskeletal 17 measurement http://www.ebi.ac.uk/efo/EFO_0802672 GCST90248184 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratin, type I cytoskeletal 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248185 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratin, type II cytoskeletal 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248186 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratin, type I cytoskeletal 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248187 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratin, type II cytoskeletal 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 keratin, type II cytoskeletal 5 measurement http://www.ebi.ac.uk/efo/EFO_0802674 GCST90248188 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratin, type II cytoskeletal 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 keratin, type II cytoskeletal 7 measurement http://www.ebi.ac.uk/efo/EFO_0802675 GCST90248189 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Keratin, type II cytoskeletal 72 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248190 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. cGMP-dependent protein kinase 1, beta isozyme levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cGMP-dependent protein kinase 1, beta isozyme measurement http://www.ebi.ac.uk/efo/EFO_0801468 GCST90248191 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kinesin-like protein KIF16B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 kinesin-like protein KIF16B measurement http://www.ebi.ac.uk/efo/EFO_0801747 GCST90248192 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dyslexia-associated protein KIAA0319-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dyslexia-associated protein KIAA0319-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802499 GCST90248193 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. KIF1-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248194 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kinesin-like protein KIF22 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248195 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kinesin-like protein KIF23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 kinesin-like protein KIF23 measurement http://www.ebi.ac.uk/efo/EFO_0020522 GCST90248196 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 32 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248319 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 4B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 leucine-rich repeat-containing protein 4B measurement http://www.ebi.ac.uk/efo/EFO_0802700 GCST90248320 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 4C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine-rich repeat-containing protein 4C measurement http://www.ebi.ac.uk/efo/EFO_0802701 GCST90248321 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 52 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248322 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 59 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248323 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 74A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 leucine-rich repeat-containing protein 74A measurement http://www.ebi.ac.uk/efo/EFO_0801763 GCST90248324 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and calponin homology domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine-rich repeat and calponin homology domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802688 GCST90248325 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and fibronectin type III domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 leucine-rich repeat and fibronectin type III domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802689 GCST90248326 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and fibronectin type-III domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine-rich repeat and fibronectin type-III domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802690 GCST90248327 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and fibronectin type-III domain-containing protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248328 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeats and immunoglobulin-like domains protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248329 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeats and immunoglobulin-like domains protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 leucine-rich repeats and immunoglobulin-like domains protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020534 GCST90248330 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802702 GCST90248331 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802703 GCST90248332 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat serine/threonine-protein kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 leucine-rich repeat serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0021876 GCST90248333 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat neuronal protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 leucine-rich repeat neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801760 GCST90248334 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat transmembrane neuronal protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 leucine-rich repeat transmembrane neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020531 GCST90248335 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat transmembrane neuronal protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine-rich repeat transmembrane neuronal protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020532 GCST90248336 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat transmembrane neuronal protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 leucine-rich repeat transmembrane neuronal protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802697 GCST90248337 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and transmembrane domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine-rich repeat and transmembrane domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802693 GCST90248338 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and transmembrane domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 leucine-rich repeat and transmembrane domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801759 GCST90248339 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Limbic system-associated membrane protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 limbic system-associated membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0020537 GCST90248340 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-binding and coiled-coil domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 calcium-binding and coiled-coil domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802356 GCST90246799 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carnitine O-acetyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246800 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90246801 Genome-wide genotyping array 2023-08-08 37029353 Jia Y 2023-04-07 BMC Psychiatry www.ncbi.nlm.nih.gov/pubmed/37029353 Association between birth by caesarian section and anxiety, self-harm: a gene-environment interaction study using UK Biobank data. Anxiety x Caesarean-section interaction 472 British ancestry cases born by C-section, 14,094 British ancestry cases not born by C-section, 1,788 British ancestry controls born by C-section, 67,261 British ancestry controls not born by C-section NA Affymetrix [NR] (imputed) 7 cesarean section, anxiety http://www.ebi.ac.uk/efo/EFO_0009636, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90275370 Genome-wide genotyping array 2023-08-08 37029353 Jia Y 2023-04-07 BMC Psychiatry www.ncbi.nlm.nih.gov/pubmed/37029353 Association between birth by caesarian section and anxiety, self-harm: a gene-environment interaction study using UK Biobank data. Self-harm x Caesarean-section interaction 471 British ancestry cases born by C-section, 13,974 British ancestry cases not born by C-section, 2,167 British ancestry controls born by C-section, 79,850 British ancestry controls not born by C-section NA Affymetrix [NR] (imputed) 19 cesarean section, Self-injurious behavior http://www.ebi.ac.uk/efo/EFO_0009636, http://purl.obolibrary.org/obo/HP_0100716 GCST90275371 Genome-wide genotyping array 2023-10-12 37768647 Zheng T 2023-09-28 J Crohns Colitis www.ncbi.nlm.nih.gov/pubmed/37768647 HLA signatures as pathophysiological discriminants of microscopic colitis subtypes. Microscopic colitis 2,599 European ancestry cases, 552,343 European ancestry controls NA Illumina [8662703] (imputed) 2 microscopic colitis http://www.ebi.ac.uk/efo/EFO_1001295 GCST90204144 Genome-wide genotyping array 2023-10-12 37768647 Zheng T 2023-09-28 J Crohns Colitis www.ncbi.nlm.nih.gov/pubmed/37768647 HLA signatures as pathophysiological discriminants of microscopic colitis subtypes. Collagenous colitis 1,498 European ancestry cases, 13,487 European ancestry controls NA Illumina [7486967] (imputed) 1 collagenous colitis http://www.ebi.ac.uk/efo/EFO_1001293 GCST90204145 Genome-wide genotyping array 2023-10-12 37768647 Zheng T 2023-09-28 J Crohns Colitis www.ncbi.nlm.nih.gov/pubmed/37768647 HLA signatures as pathophysiological discriminants of microscopic colitis subtypes. Lymphocytic colitis 373 European ancestry cases, 4,653 European ancestry controls NA Illumina [7460065] (imputed) 0 lymphocytic colitis http://www.ebi.ac.uk/efo/EFO_1001294 GCST90204146 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein NDNF levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein NDNF measurement http://www.ebi.ac.uk/efo/EFO_0802953 GCST90246927 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD109 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 CD109 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008076 GCST90246928 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Monocyte differentiation antigen CD14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246929 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD164 sialomucin-like 2 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246930 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD166 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 CD166 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020245 GCST90246931 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD177 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 13 cD177 antigen measurement http://www.ebi.ac.uk/efo/EFO_0021866 GCST90246932 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell surface glycoprotein CD200 receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cell surface glycoprotein CD200 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020253 GCST90246933 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell surface glycoprotein CD200 receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cell surface glycoprotein CD200 receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0801462 GCST90246934 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD209 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90246935 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD226 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 CD226 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020246 GCST90246936 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD27 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 CD27 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008078 GCST90246937 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD320 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246938 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte antigen CD37 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246939 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021923 GCST90246940 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD40 ligand levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST90246941 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD44 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CD44 antigen measurement http://www.ebi.ac.uk/efo/EFO_0802378 GCST90246942 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte surface antigen CD47 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leukocyte surface antigen CD47 measurement http://www.ebi.ac.uk/efo/EFO_0022010 GCST90246943 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD48 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 CD48 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020247 GCST90246944 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD59 glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CD59 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0021924 GCST90246945 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD5 antigen-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 CD5 antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0020248 GCST90246946 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD63 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 CD63 antigen measurement http://www.ebi.ac.uk/efo/EFO_0022033 GCST90246947 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Early activation antigen CD69 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246948 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B-cell differentiation antigen CD72 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246949 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD9 antigen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246950 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement decay-accelerating factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 complement decay-accelerating factor measurement http://www.ebi.ac.uk/efo/EFO_0008095 GCST90246951 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CUB domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 CUB domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802432 GCST90246952 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-related family member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cadherin-related family member 1 measurement http://www.ebi.ac.uk/efo/EFO_0801439 GCST90246953 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-related family member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cadherin-related family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802352 GCST90246954 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-related family member 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 cadherin-related family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801440 GCST90246955 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CDK5 and ABL1 enzyme substrate 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246956 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase 5:Cyclin-dependent kinase 5 activator 1 complex levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cyclin-dependent kinase 5:cyclin-dependent kinase 5 activator 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020296 GCST90246957 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase 8:Cyclin-C complex levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cyclin-dependent kinase 8:cyclin-c complex measurement http://www.ebi.ac.uk/efo/EFO_0020297 GCST90246958 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase 2-associated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cyclin-dependent kinase 2-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802440 GCST90246959 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase 2-associated protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246960 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase inhibitor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246961 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase inhibitor 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cyclin-dependent kinase inhibitor 1b measurement http://www.ebi.ac.uk/efo/EFO_0020298 GCST90246962 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase inhibitor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cyclin-dependent kinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802442 GCST90246963 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase 4 inhibitor B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cyclin-dependent kinase 4 inhibitor B measurement http://www.ebi.ac.uk/efo/EFO_0802441 GCST90246964 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase 4 inhibitor C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246965 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinase 4 inhibitor D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246966 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cerebral dopamine neurotrophic factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90246967 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell adhesion molecule-related/down-regulated by oncogenes levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cell adhesion molecule-related/down-regulated by oncogenes measurement http://www.ebi.ac.uk/efo/EFO_0008079 GCST90246968 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chromodomain Y-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246969 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carcinoembryonic antigen-related cell adhesion molecule 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246970 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carcinoembryonic antigen-related cell adhesion molecule 20 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246971 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carcinoembryonic antigen-related cell adhesion molecule 21 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 carcinoembryonic antigen-related cell adhesion molecule 21 measurement http://www.ebi.ac.uk/efo/EFO_0802369 GCST90246972 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carcinoembryonic antigen-related cell adhesion molecule 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246973 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carcinoembryonic antigen-related cell adhesion molecule 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246974 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carcinoembryonic antigen-related cell adhesion molecule 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246975 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytosolic endo-beta-N-acetylglucosaminidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246976 Genome-wide genotyping array 2023-04-26 36652833 David FS 2023-01-16 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/36652833 Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Paranoid-hallucinatory syndrome in major depressive disorder, bipolar disorder or schizophrenia spectrum disorders 1,042 individuals 816 individuals Illumina [8565143] (imputed) 0 schizophrenia symptom severity measurement http://www.ebi.ac.uk/efo/EFO_0007927 GCST90267999 Genome-wide genotyping array 2023-04-26 36652833 David FS 2023-01-16 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/36652833 Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Negative syndrome in major depressive disorder, bipolar disorder or schizophrenia spectrum disorders 1,042 individuals 816 individuals Illumina [8565143] (imputed) 0 schizophrenia symptom severity measurement http://www.ebi.ac.uk/efo/EFO_0007927 GCST90268000 Genome-wide genotyping array 2023-04-26 36652833 David FS 2023-01-16 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/36652833 Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Depression in major depressive disorder, bipolar disorder or schizophrenia spectrum disorders 1,042 individuals 816 individuals Illumina [8565143] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90268001 Genome-wide genotyping array 2023-04-26 36652833 David FS 2023-01-16 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/36652833 Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Positive formal thought disorder in major depressive disorder, bipolar disorder or schizophrenia spectrum disorders 1,042 individuals 816 individuals Illumina [8565143] (imputed) 0 formal thought disorder http://www.ebi.ac.uk/efo/EFO_0004805 GCST90268002 Genome-wide genotyping array 2023-04-26 36652833 David FS 2023-01-16 Schizophr Res www.ncbi.nlm.nih.gov/pubmed/36652833 Genetic contributions to transdiagnostic symptom dimensions in patients with major depressive disorder, bipolar disorder, and schizophrenia spectrum disorders. Increased appetite in major depressive disorder, bipolar disorder or schizophrenia spectrum disorders 1,042 individuals 816 individuals Illumina [8565143] (imputed) 0 eating behaviour http://www.ebi.ac.uk/efo/EFO_0007829 GCST90268003 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptic vesicle glycoprotein 2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 synaptic vesicle glycoprotein 2A measurement http://www.ebi.ac.uk/efo/EFO_0803115 GCST90249741 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptic vesicle membrane protein VAT-1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249742 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803113 GCST90249743 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small VCP/p97-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249744 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Switch-associated protein 70 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 switch-associated protein 70 measurement http://www.ebi.ac.uk/efo/EFO_0802107 GCST90249745 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptotagmin-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 synaptotagmin-11 measurement http://www.ebi.ac.uk/efo/EFO_0802108 GCST90249746 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptotagmin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249747 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptotagmin-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 synaptotagmin-5 measurement http://www.ebi.ac.uk/efo/EFO_0803120 GCST90249748 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptotagmin-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 synaptotagmin-7 measurement http://www.ebi.ac.uk/efo/EFO_0803121 GCST90249749 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptotagmin-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 synaptotagmin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803123 GCST90249750 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptotagmin-like protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 synaptotagmin-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802109 GCST90249751 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 106A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249752 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 106B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249753 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Type 2 lactosamine alpha-2,3-sialyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 type 2 lactosamine alpha-2,3-sialyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802170 GCST90249754 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transformer-2 protein homolog beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transformer-2 protein homolog beta measurement http://www.ebi.ac.uk/efo/EFO_0802143 GCST90249755 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tropomyosin alpha-1 chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tropomyosin alpha-1 chain measurement http://www.ebi.ac.uk/efo/EFO_0020786 GCST90249756 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Translational activator of cytochrome c oxidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249757 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell surface protein tactile levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 T-cell surface protein tactile measurement http://www.ebi.ac.uk/efo/EFO_0802115 GCST90249758 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TAR DNA-binding protein 43 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249759 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription initiation factor TFIID subunit 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249760 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transgelin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transgelin measurement http://www.ebi.ac.uk/efo/EFO_0803171 GCST90249761 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transgelin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 transgelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021884 GCST90249762 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcriptional activator protein Pur-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transcriptional activator protein Pur-alpha measurement http://www.ebi.ac.uk/efo/EFO_0803165 GCST90249763 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcriptional activator protein Pur-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249764 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Translocon-associated protein subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 translocon-associated protein subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0803173 GCST90249765 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tax1-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tax1-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803138 GCST90249766 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TATA-binding protein-associated factor 2N levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249767 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tropomyosin beta chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tropomyosin beta chain measurement http://www.ebi.ac.uk/efo/EFO_0020787 GCST90249768 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tubulin-specific chaperone A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tubulin-specific chaperone A measurement http://www.ebi.ac.uk/efo/EFO_0802166 GCST90249769 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tubulin-folding cofactor B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249770 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tubulin-specific chaperone E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tubulin-specific chaperone E measurement http://www.ebi.ac.uk/efo/EFO_0802167 GCST90249771 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thyroxine-Binding Globulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 thyroxine-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0009172 GCST90249772 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transducin beta-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249773 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TATA-box-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tata-box-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020764 GCST90249774 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TATA box-binding protein-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249775 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TGF-beta receptor type-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tgf-beta receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020767 GCST90249776 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-box transcription factor TBX5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 t-box transcription factor TBX5 measurement http://www.ebi.ac.uk/efo/EFO_0803129 GCST90249777 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell surface glycoprotein CD1a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249778 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell surface glycoprotein CD3 epsilon chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 10 T-cell surface glycoprotein CD3 epsilon chain measurement http://www.ebi.ac.uk/efo/EFO_0802114 GCST90249779 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell surface glycoprotein CD3 gamma chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 t-cell surface glycoprotein CD3 gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0803133 GCST90249780 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell surface glycoprotein CD5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 t-cell surface glycoprotein CD5 measurement http://www.ebi.ac.uk/efo/EFO_0803134 GCST90249781 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell antigen CD7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249782 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-lymphocyte activation antigen CD86 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 t-lymphocyte activation antigen CD86 measurement http://www.ebi.ac.uk/efo/EFO_0020762 GCST90249783 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell surface glycoprotein CD8 alpha chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249784 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell surface glycoprotein CD8 beta chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 t-cell surface glycoprotein CD8 beta chain measurement http://www.ebi.ac.uk/efo/EFO_0803135 GCST90249785 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell leukemia/lymphoma protein 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249786 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-complex protein 11 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249787 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-complex protein 1 subunit epsilon levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249788 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-complex protein 1 subunit theta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249789 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-complex protein 1 subunit eta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249790 Genome-wide genotyping array 2023-10-17 37803156 Tegegne BS 2023-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37803156 Phenotypic but not genetically predicted heart rate variability associated with all-cause mortality. Heart rate variability (corrected root mean square of successive differences) 46,075 European ancestry individuals NA Affymetrix [19376764] (imputed) 13 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST90281264 Genome-wide genotyping array 2023-10-17 37803156 Tegegne BS 2023-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37803156 Phenotypic but not genetically predicted heart rate variability associated with all-cause mortality. Heart rate variability (standard deviation of normal-to-normal intervals) 46,075 European ancestry individuals NA Affymetrix [19376764] (imputed) 9 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST90281265 Genome-wide genotyping array 2023-10-17 37803156 Tegegne BS 2023-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37803156 Phenotypic but not genetically predicted heart rate variability associated with all-cause mortality. Heart rate variability (corrected standard deviation of normal-to-normal intervals) 46,075 European ancestry individuals NA Affymetrix [19376764] (imputed) 7 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST90281266 Genome-wide genotyping array 2023-10-17 37803156 Tegegne BS 2023-10-06 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37803156 Phenotypic but not genetically predicted heart rate variability associated with all-cause mortality. Heart rate variability (root mean square of successive differences) 46,075 European ancestry individuals NA Affymetrix [19376764] (imputed) 16 heart rate variability measurement http://www.ebi.ac.uk/efo/EFO_0008003 GCST90281263 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription factor IIIB 90 kDa subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 transcription factor IIIb 90 kda subunit measurement http://www.ebi.ac.uk/efo/EFO_0020778 GCST90249811 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription factor AP-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 transcription factor AP-1 measurement http://www.ebi.ac.uk/efo/EFO_0021909 GCST90249812 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trefoil factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 trefoil factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021865 GCST90249813 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trefoil factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 trefoil factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0021846 GCST90249814 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trefoil factor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90249815 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor alpha-induced protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor necrosis factor alpha-induced protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803200 GCST90249816 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor alpha-induced protein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249817 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription factor jun-D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249818 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90249819 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tumor necrosis factor ligand superfamily member 12 measurement http://www.ebi.ac.uk/efo/EFO_0010801 GCST90249820 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 13B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor necrosis factor ligand superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020793 GCST90249821 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90249822 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90249823 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tumor necrosis factor ligand superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020795 GCST90249824 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 6, soluble form levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor ligand superfamily member 6, soluble form measurement http://www.ebi.ac.uk/efo/EFO_0020797 GCST90249825 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor ligand superfamily member 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90249826 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tuftelin-interacting protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tuftelin-interacting protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0803199 GCST90249827 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tissue factor pathway inhibitor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90249828 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tissue factor pathway inhibitor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tissue factor pathway inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0803156 GCST90249829 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription factor RelB levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 transcription factor RelB measurement http://www.ebi.ac.uk/efo/EFO_0802140 GCST90249830 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 10B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 10B measurement http://www.ebi.ac.uk/efo/EFO_0021993 GCST90249831 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 10D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor necrosis factor receptor superfamily member 10D measurement http://www.ebi.ac.uk/efo/EFO_0021942 GCST90249832 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 11B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 11B measurement http://www.ebi.ac.uk/efo/EFO_0020801 GCST90249833 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 13B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020803 GCST90249834 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 17 measurement http://www.ebi.ac.uk/efo/EFO_0020806 GCST90249835 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitochondrial ubiquitin ligase activator of NFKB 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 mitochondrial ubiquitin ligase activator of NFKB 1 measurement http://www.ebi.ac.uk/efo/EFO_0801804 GCST90248670 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear factor NF-kappa-B p105 subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248671 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NF-kappa-B inhibitor delta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248672 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurofilament light polypeptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248673 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NFU1 iron-sulfur cluster scaffold homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 NFU1 iron-sulfur cluster scaffold homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802810 GCST90248674 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NHP2-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 NHP2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801840 GCST90248675 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Non-homologous end-joining factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 non-homologous end-joining factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802817 GCST90248676 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NHL repeat-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 NHL repeat-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801839 GCST90248677 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nidogen-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 nidogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008249 GCST90248678 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nidogen-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90248679 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Magnesium transporter NIPA4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 magnesium transporter NIPA4 measurement http://www.ebi.ac.uk/efo/EFO_0802723 GCST90248680 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tomoregulin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249797 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tenascin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 27 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249798 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Teneurin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249799 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Teneurin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 teneurin-3 measurement http://www.ebi.ac.uk/efo/EFO_0803140 GCST90249800 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Teneurin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 teneurin-4 measurement http://www.ebi.ac.uk/efo/EFO_0803141 GCST90249801 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tenascin-R levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tenascin-R measurement http://www.ebi.ac.uk/efo/EFO_0803139 GCST90249802 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tenascin-X levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249803 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Telomeric repeat-binding factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249804 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Testin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249805 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcriptional enhancer factor TEF-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transcriptional enhancer factor TEF-3 measurement http://www.ebi.ac.uk/efo/EFO_0803166 GCST90249806 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcriptional enhancer factor TEF-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transcriptional enhancer factor TEF-5 measurement http://www.ebi.ac.uk/efo/EFO_0803167 GCST90249807 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tetranectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tetranectin measurement http://www.ebi.ac.uk/efo/EFO_0020957 GCST90249808 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Testis-expressed sequence 29 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 testis-expressed sequence 29 protein measurement http://www.ebi.ac.uk/efo/EFO_0802125 GCST90249809 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tissue factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tissue factor measurement http://www.ebi.ac.uk/efo/EFO_0010623 GCST90249810 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ornithine decarboxylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ornithine decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0802835 GCST90248790 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ornithine decarboxylase antizyme 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ornithine decarboxylase antizyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0802834 GCST90248791 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oligoribonuclease, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 oligoribonuclease, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802831 GCST90248792 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Orphan sodium- and chloride-dependent neurotransmitter transporter NTT5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 orphan sodium- and chloride-dependent neurotransmitter transporter NTT5 measurement http://www.ebi.ac.uk/efo/EFO_0802836 GCST90248793 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Orexigenic neuropeptide QRFP levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 orexigenic neuropeptide QRFP measurement http://www.ebi.ac.uk/efo/EFO_0802832 GCST90248794 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oncostatin-M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90248795 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oncostatin-M-specific receptor subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 oncostatin-M-specific receptor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801860 GCST90248796 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Osteocalcin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90248797 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Osteopontin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 osteopontin measurement http://www.ebi.ac.uk/efo/EFO_0021776 GCST90248798 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Osteoclast-stimulating factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248799 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ornithine carbamoyltransferase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248800 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Otoraplin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248801 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. OTU domain-containing protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248802 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ovarian cancer G-protein coupled receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248803 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Esterase OVCA2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248804 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. OX-2 membrane glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 OX-2 membrane glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008253 GCST90248805 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oxidized Protein deglycase DJ-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248806 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oxidoreductase HTATIP2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 oxidoreductase HTATIP2 measurement http://www.ebi.ac.uk/efo/EFO_0801863 GCST90248807 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248808 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 14-3-3 protein family levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 14-3-3 protein family measurement http://www.ebi.ac.uk/efo/EFO_0020109 GCST90246374 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 14-3-3 protein beta/alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 14-3-3 protein beta/alpha measurement http://www.ebi.ac.uk/efo/EFO_0021957 GCST90246375 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 14-3-3 protein sigma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 14-3-3 protein sigma measurement http://www.ebi.ac.uk/efo/EFO_0020110 GCST90246376 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 15-hydroxyprostaglandin dehydrogenase [NAD(+)] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 15-hydroxyprostaglandin dehydrogenase [NAD(+)] measurement http://www.ebi.ac.uk/efo/EFO_0020111 GCST90246377 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-hydroxyanthranilate 3,4-dioxygenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 3-hydroxyanthranilate 3,4-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0021862 GCST90246378 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5-hydroxytryptamine receptor 2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246379 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexophilin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90248765 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexophilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248766 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexophilin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neurexophilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802798 GCST90248767 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Out at first protein homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 out at first protein homolog measurement http://www.ebi.ac.uk/efo/EFO_0801862 GCST90248768 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 2-5-oligoadenylate synthase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 2'-5'-oligoadenylate synthase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021911 GCST90248769 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Opioid-binding protein/cell adhesion molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 opioid-binding protein/cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020618 GCST90248770 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Obg-like ATPase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 obg-like ATPase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801858 GCST90248771 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Odorant-binding protein 2a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 odorant-binding protein 2a measurement http://www.ebi.ac.uk/efo/EFO_0802828 GCST90248772 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Odorant-binding protein 2b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 odorant-binding protein 2b measurement http://www.ebi.ac.uk/efo/EFO_0801859 GCST90248773 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. OCIA domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 OCIA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008252 GCST90248774 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol polyphosphate 5-phosphatase OCRL-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 inositol polyphosphate 5-phosphatase OCRL-1 measurement http://www.ebi.ac.uk/efo/EFO_0801699 GCST90248775 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oncoprotein-induced transcript 3 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248776 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Olfactomedin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 olfactomedin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020617 GCST90248777 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Olfactomedin-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 olfactomedin-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802829 GCST90248778 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oligophrenin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 oligophrenin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802830 GCST90248779 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Osteomodulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 osteomodulin measurement http://www.ebi.ac.uk/efo/EFO_0020619 GCST90248780 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase omega-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glutathione S-transferase omega-1 measurement http://www.ebi.ac.uk/efo/EFO_0801639 GCST90248781 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oligodendrocyte-myelin glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248782 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Olfactory marker protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248783 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oocyte-secreted protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248784 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Opalin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 opalin measurement http://www.ebi.ac.uk/efo/EFO_0801861 GCST90248785 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Opiorphin prepropeptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248786 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Opticin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248787 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. O-phosphoseryl-tRNA(Sec) selenium transferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248788 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oral cancer-overexpressed protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248789 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pro-FMRFamide-related neuropeptide FF levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pro-FMRFamide-related neuropeptide FF measurement http://www.ebi.ac.uk/efo/EFO_0801911 GCST90248715 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear protein localization protein 4 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear protein localization protein 4 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801851 GCST90248716 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleophosmin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248717 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear pore complex-interacting protein family member B3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 nuclear pore complex-interacting protein family member B3 measurement http://www.ebi.ac.uk/efo/EFO_0801850 GCST90248718 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroplastin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248719 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuronal pentraxin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 neuronal pentraxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801833 GCST90248720 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuronal pentraxin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 neuronal pentraxin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801834 GCST90248721 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuronal pentraxin receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248722 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear receptor subfamily 1 group D member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear receptor subfamily 1 group d member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020614 GCST90248723 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear receptor subfamily 1 group D member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear receptor subfamily 1 group D member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801853 GCST90248724 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Natural cytotoxicity triggering receptor 3 ligand 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 natural cytotoxicity triggering receptor 3 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0802787 GCST90248725 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear receptor subfamily 5 group A member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear receptor subfamily 5 group A member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802825 GCST90248726 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nutritionally-regulated adipose and cardiac enriched protein homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 nutritionally-regulated adipose and cardiac enriched protein homolog measurement http://www.ebi.ac.uk/efo/EFO_0803300 GCST90248727 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutral and basic amino acid transport protein rBAT levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248728 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear receptor-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 nuclear receptor-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801854 GCST90248729 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuronal cell adhesion molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neuronal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020602 GCST90248730 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nicotinamide riboside kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248731 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuropilin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 neuropilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020603 GCST90248732 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuropilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neuropilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801836 GCST90248733 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 neurexin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801829 GCST90248734 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexin-1-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neurexin-1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020596 GCST90248735 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexin-2-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neurexin-2-beta measurement http://www.ebi.ac.uk/efo/EFO_0802797 GCST90248736 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248737 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurexin-3-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neurexin-3-beta measurement http://www.ebi.ac.uk/efo/EFO_0020597 GCST90248738 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclease-sensitive element-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248739 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NSFL1 cofactor p47 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248740 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NT-3 growth factor receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 nt-3 growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020613 GCST90248741 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5(3)-deoxyribonucleotidase, cytosolic type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248742 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5-nucleotidase domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248743 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5(3)-deoxyribonucleotidase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248744 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-terminal pro-BNP levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 N-terminal pro-BNP measurement http://www.ebi.ac.uk/efo/EFO_0022014 GCST90248745 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NTF2-related export protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 NTF2-related export protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801847 GCST90248746 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NTF2-related export protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248747 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-terminal Xaa-Pro-Lys N-methyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 n-terminal Xaa-Pro-Lys N-methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801820 GCST90248748 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Netrin-G1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 netrin-G1 measurement http://www.ebi.ac.uk/efo/EFO_0801825 GCST90248749 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Natural cytotoxicity triggering receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90248750 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Natural cytotoxicity triggering receptor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 natural cytotoxicity triggering receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008243 GCST90248751 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurotrimin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248752 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleosome-remodeling factor subunit BPTF levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248753 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleobindin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248754 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxisomal NADH pyrophosphatase NUDT12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peroxisomal NADH pyrophosphatase NUDT12 measurement http://www.ebi.ac.uk/efo/EFO_0801878 GCST90248755 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NudC domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 NudC domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020616 GCST90248756 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribose pyrophosphatase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ADP-ribose pyrophosphatase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801349 GCST90248757 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Netrin receptor UNC5B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 netrin receptor UNC5B measurement http://www.ebi.ac.uk/efo/EFO_0802792 GCST90248758 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Netrin receptor UNC5C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 netrin receptor UNC5C measurement http://www.ebi.ac.uk/efo/EFO_0020590 GCST90248759 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Netrin receptor UNC5D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90248760 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear pore complex protein Nup98-Nup96 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248761 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleolysin TIAR levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248762 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NEDD4-like E3 ubiquitin-protein ligase WWP1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248763 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear RNA export factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear RNA export factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801855 GCST90248764 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amyloid beta A4 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 amyloid beta A4 protein measurement http://www.ebi.ac.uk/efo/EFO_0020145 GCST90246497 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acidic leucine-rich nuclear phosphoprotein 32 family member A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 acidic leucine-rich nuclear phosphoprotein 32 family member A measurement http://www.ebi.ac.uk/efo/EFO_0802250 GCST90246498 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acidic leucine-rich nuclear phosphoprotein 32 family member B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 acidic leucine-rich nuclear phosphoprotein 32 family member b measurement http://www.ebi.ac.uk/efo/EFO_0020125 GCST90246499 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Atrial natriuretic factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 atrial natriuretic factor measurement http://www.ebi.ac.uk/efo/EFO_0004789 GCST90246500 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiogenin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90246501 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiopoietin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 angiopoietin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020146 GCST90246502 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiopoietin-1 receptor, soluble levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 angiopoietin-1 receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008023 GCST90246503 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiopoietin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90246504 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiostatin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 angiostatin measurement http://www.ebi.ac.uk/efo/EFO_0008024 GCST90246505 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiotensinogen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 angiotensinogen measurement http://www.ebi.ac.uk/efo/EFO_0008025 GCST90246506 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiopoietin-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 angiopoietin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801382 GCST90246507 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiopoietin-related protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 angiopoietin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020148 GCST90246508 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiopoietin-related protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 angiopoietin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020149 GCST90246509 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiopoietin-related protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 angiopoietin-related protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802280 GCST90246510 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ankyrin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246511 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ankyrin repeat domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246512 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Anosmin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 anosmin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802284 GCST90246513 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ankyrin repeat domain-containing protein 27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ankyrin repeat domain-containing protein 27 measurement http://www.ebi.ac.uk/efo/EFO_0802281 GCST90246514 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ankyrin repeat domain-containing protein 54 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246515 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Anthrax toxin receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246516 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Anthrax toxin receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246517 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 annexin A10 measurement http://www.ebi.ac.uk/efo/EFO_0801383 GCST90246518 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246519 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246520 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 annexin A1 measurement http://www.ebi.ac.uk/efo/EFO_0008026 GCST90246521 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldo-keto reductase family 1 member C4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246472 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenylate kinase isoenzyme 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246473 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A-kinase anchor protein 7 isoforms alpha and beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246474 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Antileukoproteinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 antileukoproteinase measurement http://www.ebi.ac.uk/efo/EFO_0020154 GCST90246475 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldehyde dehydrogenase family 1 member A3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246476 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldehyde dehydrogenase family 3 member B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 aldehyde dehydrogenase family 3 member B1 measurement http://www.ebi.ac.uk/efo/EFO_0801361 GCST90246477 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aromatic-L-amino-acid decarboxylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246478 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alanine--tRNA ligase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alanine--tRNA ligase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0801359 GCST90246479 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aspartate--tRNA ligase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246480 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldehyde dehydrogenase, dimeric NADP-preferring levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 aldehyde dehydrogenase, dimeric NADP-preferring measurement http://www.ebi.ac.uk/efo/EFO_0801362 GCST90246481 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldehyde dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246482 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldose reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 aldose reductase measurement http://www.ebi.ac.uk/efo/EFO_0801364 GCST90246483 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldo-keto reductase family 1 member B10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246484 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246485 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aspartate--tRNA ligase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246486 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alkaline phosphatase, tissue-nonspecific isozyme levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246487 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alkaline phosphatase, placental type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246488 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alanine aminotransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 alanine aminotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802260 GCST90246489 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amphoterin-induced protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 amphoterin-induced protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021949 GCST90246490 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aminoacylase-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246491 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aminopeptidase N levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246492 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aminopeptidase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246493 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AMP Kinase (alpha1beta1gamma1) levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 amp kinase (alpha1beta1gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020142 GCST90246494 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AMP Kinase (alpha2beta2gamma1) levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 amp kinase (alpha2beta2gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020143 GCST90246495 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aspartate aminotransferase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 aspartate aminotransferase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0008031 GCST90246496 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Nonanoic acid (pelargonate) 243 individuals NA NR [811782] (imputed) 5 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267512 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Phe (uM) 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267513 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Putrescine (uM) 243 individuals NA NR [811782] (imputed) 1 putrescine measurement http://www.ebi.ac.uk/efo/EFO_0021810 GCST90267514 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Pyridoxal 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267515 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Pyridoxamine 243 individuals NA NR [811782] (imputed) 1 pyridoxamine measurement http://www.ebi.ac.uk/efo/EFO_0021837 GCST90267516 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Pyridoxamine 5'-phosphate 243 individuals NA NR [811782] (imputed) 1 pyridoxamine measurement http://www.ebi.ac.uk/efo/EFO_0021837 GCST90267517 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Pyruvate 243 individuals NA NR [811782] (imputed) 4 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90267518 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Pyruvate (uM) 243 individuals NA NR [811782] (imputed) 128 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90267519 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of S-Adenosyl-L-homocysteine 243 individuals NA NR [811782] (imputed) 1 S-(5-Adenosy)-L-homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0021666 GCST90267520 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of S-Adenosyl-L-methionine 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267521 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Sorbitol 243 individuals NA NR [811782] (imputed) 7 sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0010533 GCST90267522 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Spermidine 243 individuals NA NR [811782] (imputed) 1 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90267523 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Spermidine (uM) 243 individuals NA NR [811782] (imputed) 1 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90267524 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Spermine 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267525 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Spermine (uM) 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267526 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Sphingosine 1-phosphate 243 individuals NA NR [811782] (imputed) 11 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90267527 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Taurine 243 individuals NA NR [811782] (imputed) 1 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90267528 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Tetradecanoic acid 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267529 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Threonine 243 individuals NA NR [811782] (imputed) 1 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90267530 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of UDP 243 individuals NA NR [811782] (imputed) 1 uridine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010545 GCST90267531 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of UDP-N-acetyl-D-glucosamine 243 individuals NA NR [811782] (imputed) 6 uridine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010545 GCST90267532 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Undecanoyl carnitine 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267533 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Urate (uM) 243 individuals NA NR [811782] (imputed) 11 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90267534 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPAF18:0 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267535 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of LPS20:4 243 individuals NA NR [811782] (imputed) 1 lysophosphatidylserine measurement http://www.ebi.ac.uk/efo/EFO_0020048 GCST90267536 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Attractin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246619 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ataxin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246620 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Augurin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 augurin measurement http://www.ebi.ac.uk/efo/EFO_0801399 GCST90246621 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aurora kinase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 aurora kinase A measurement http://www.ebi.ac.uk/efo/EFO_0020168 GCST90246622 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aurora kinase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 aurora kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020169 GCST90246623 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Axin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 axin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801400 GCST90246624 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Azurocidin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 azurocidin measurement http://www.ebi.ac.uk/efo/EFO_0020170 GCST90246625 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-2-glycoprotein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246626 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bcl-2-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 BCL-2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020177 GCST90246627 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bcl-2-like protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246628 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bcl-2-like protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246629 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bcl-2-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 bcl-2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021928 GCST90246630 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-2-microglobulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 11 beta-2-microglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020180 GCST90246631 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,3-glucosyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-1,3-glucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802310 GCST90246632 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0803220 GCST90246633 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 measurement http://www.ebi.ac.uk/efo/EFO_0802184 GCST90246634 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,3-galactosyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246635 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,3-galactosyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246636 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,3-galactosyltransferase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-1,3-galactosyltransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0802309 GCST90246637 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bifunctional 3-phosphoadenosine 5-phosphosulfate synthase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246638 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,4-galactosyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 beta-1,4-galactosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801409 GCST90246639 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,4-galactosyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 beta-1,4-galactosyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801410 GCST90246640 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,4-galactosyltransferase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 beta-1,4-galactosyltransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0801411 GCST90246641 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,4-galactosyltransferase 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 beta-1,4-galactosyltransferase 7 measurement http://www.ebi.ac.uk/efo/EFO_0802314 GCST90246642 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-arrestin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-arrestin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801413 GCST90246643 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bcl2-associated agonist of cell death levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 bcl2-associated agonist of cell death measurement http://www.ebi.ac.uk/efo/EFO_0021998 GCST90246644 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BAG family molecular chaperone regulator 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246645 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BAG family molecular chaperone regulator 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 BAG family molecular chaperone regulator 3 measurement http://www.ebi.ac.uk/efo/EFO_0802302 GCST90246646 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BAG family molecular chaperone regulator 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 BAG family molecular chaperone regulator 4 measurement http://www.ebi.ac.uk/efo/EFO_0802303 GCST90246647 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BAG family molecular chaperone regulator 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246648 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adhesion G protein-coupled receptor B3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246649 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Brain-specific angiogenesis inhibitor 1-associated protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246650 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-Ala-His dipeptidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 beta-Ala-His dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0008033 GCST90246651 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BMP and activin membrane-bound inhibitor homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246652 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B-cell receptor-associated protein 29 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 B-cell receptor-associated protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0802301 GCST90246653 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B-cell antigen receptor complex-associated protein alpha chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 B-cell antigen receptor complex-associated protein alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0801402 GCST90246654 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BRCA1-associated RING domain protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 BRCA1-associated RING domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802337 GCST90246655 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. beta-adrenergic receptor kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-adrenergic receptor kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020181 GCST90246656 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Basic leucine zipper transcriptional factor ATF-like 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 basic leucine zipper transcriptional factor ATF-like 3 measurement http://www.ebi.ac.uk/efo/EFO_0801404 GCST90246657 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Basal Cell Adhesion Molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 basal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008032 GCST90246658 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Breast cancer anti-estrogen resistance protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 breast cancer anti-estrogen resistance protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008040 GCST90246659 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Branched-chain-amino-acid aminotransferase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246660 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-crystallin B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246661 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-crystallin B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-crystallin B2 measurement http://www.ebi.ac.uk/efo/EFO_0801414 GCST90246662 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B-cell lymphoma/leukemia 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 B-cell lymphoma/leukemia 10 measurement http://www.ebi.ac.uk/efo/EFO_0801403 GCST90246663 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B-cell lymphoma 6 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 B-cell lymphoma 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0021933 GCST90246664 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-crystallin S levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246665 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 beta-defensin 1 measurement http://www.ebi.ac.uk/efo/EFO_0801415 GCST90246666 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 104 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 104 measurement http://www.ebi.ac.uk/efo/EFO_0801416 GCST90246667 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 106 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-defensin 106 measurement http://www.ebi.ac.uk/efo/EFO_0802316 GCST90246668 Genome-wide genotyping array 2023-05-31 36641522 Sinkala M 2023-01-14 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36641522 A genome-wide association study identifies distinct variants associated with pulmonary function among European and African ancestries from the UK Biobank. FEV1 5,978 African ancestry individuals NA NR [NR] (imputed) 1 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90270080 Genome-wide genotyping array 2023-05-31 36641522 Sinkala M 2023-01-14 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36641522 A genome-wide association study identifies distinct variants associated with pulmonary function among European and African ancestries from the UK Biobank. FEV1 383,471 European ancestry individuals NA NR [NR] (imputed) 200 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90270081 Genome-wide genotyping array 2023-05-31 36641522 Sinkala M 2023-01-14 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36641522 A genome-wide association study identifies distinct variants associated with pulmonary function among European and African ancestries from the UK Biobank. FVC 5,978 African ancestry individuals NA NR [NR] (imputed) 2 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90270082 Genome-wide genotyping array 2023-05-31 36641522 Sinkala M 2023-01-14 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36641522 A genome-wide association study identifies distinct variants associated with pulmonary function among European and African ancestries from the UK Biobank. FVC 383,471 European ancestry individuals NA NR [NR] (imputed) 218 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90270083 Genome-wide genotyping array 2023-05-31 36641522 Sinkala M 2023-01-14 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36641522 A genome-wide association study identifies distinct variants associated with pulmonary function among European and African ancestries from the UK Biobank. Peak expiratory flow 5,978 African ancestry individuals NA NR [NR] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90270084 Genome-wide genotyping array 2023-05-31 36641522 Sinkala M 2023-01-14 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36641522 A genome-wide association study identifies distinct variants associated with pulmonary function among European and African ancestries from the UK Biobank. Peak expiratory flow 383,471 European ancestry individuals NA NR [NR] (imputed) 199 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90270085 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit beta type-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249136 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit beta type-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249137 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit beta type-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249138 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit beta type-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 proteasome subunit beta type-5 measurement http://www.ebi.ac.uk/efo/EFO_0802923 GCST90249139 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome subunit beta type-9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249140 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PH and SEC7 domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 PH and SEC7 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803302 GCST90249141 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 26S proteasome non-ATPase regulatory subunit 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249142 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PH and SEC7 domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 PH and SEC7 domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803295 GCST90249143 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 26S proteasome non-ATPase regulatory subunit 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 26s proteasome non-atpase regulatory subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0020112 GCST90249144 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. P-selectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90249145 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249146 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pregnancy-specific beta-1-glycoprotein 11 measurement http://www.ebi.ac.uk/efo/EFO_0802895 GCST90249147 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pregnancy-specific beta-1-glycoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802896 GCST90249148 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 pregnancy-specific beta-1-glycoprotein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801906 GCST90249149 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pregnancy-specific beta-1-glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801907 GCST90249150 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 pregnancy-specific beta-1-glycoprotein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801908 GCST90249151 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Putative pregnancy-specific beta-1-glycoprotein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 putative pregnancy-specific beta-1-glycoprotein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802983 GCST90249152 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pregnancy-specific beta-1-glycoprotein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802898 GCST90249153 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy-specific beta-1-glycoprotein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pregnancy-specific beta-1-glycoprotein 9 measurement http://www.ebi.ac.uk/efo/EFO_0801909 GCST90249154 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. P-selectin glycoprotein ligand 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 P-selectin glycoprotein ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0010922 GCST90249155 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 26S proteasome non-ATPase regulatory subunit 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 26S proteasome non-ATPase regulatory subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0802235 GCST90249156 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 26S proteasome non-ATPase regulatory subunit 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 26S proteasome non-ATPase regulatory subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0801331 GCST90249157 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 26S proteasome non-ATPase regulatory subunit 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249158 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 112 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 112 measurement http://www.ebi.ac.uk/efo/EFO_0801418 GCST90246672 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 113 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 113 measurement http://www.ebi.ac.uk/efo/EFO_0802320 GCST90246673 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 116 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-defensin 116 measurement http://www.ebi.ac.uk/efo/EFO_0802322 GCST90246674 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 119 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-defensin 119 measurement http://www.ebi.ac.uk/efo/EFO_0801419 GCST90246675 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 121 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-defensin 121 measurement http://www.ebi.ac.uk/efo/EFO_0802324 GCST90246676 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 128 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 128 measurement http://www.ebi.ac.uk/efo/EFO_0801420 GCST90246677 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 129 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246678 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 132 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246679 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 135 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 135 measurement http://www.ebi.ac.uk/efo/EFO_0802328 GCST90246680 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 136 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-defensin 136 measurement http://www.ebi.ac.uk/efo/EFO_0802329 GCST90246681 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 4A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246682 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-hydroxybutyrate dehydrogenase type 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246683 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Brain-derived neurotrophic factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST90246684 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BDNF/NT-3 growth factors receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 bdnf/nt-3 growth factors receptor measurement http://www.ebi.ac.uk/efo/EFO_0020179 GCST90246685 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beclin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beclin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802306 GCST90246686 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-endorphin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90246687 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-enolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246688 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BET1-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 BET1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802307 GCST90246689 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-casein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246690 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-galactoside alpha-2,6-sialyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-galactoside alpha-2,6-sialyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802330 GCST90246691 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bcl-2-related protein A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 BCL-2-related protein A1 measurement http://www.ebi.ac.uk/efo/EFO_0020178 GCST90246692 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-glucuronidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246693 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Biglycan levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 biglycan measurement http://www.ebi.ac.uk/efo/EFO_0020182 GCST90246694 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BH3-interacting domain death agonist levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 BH3-interacting domain death agonist measurement http://www.ebi.ac.uk/efo/EFO_0021994 GCST90246695 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-hexosaminidase subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246696 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. S-methylmethionine--homocysteine S-methyltransferase BHMT2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246697 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Baculoviral IAP repeat-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246698 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatocyte growth factor receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 hepatocyte growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0008153 GCST90247878 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hedgehog-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247879 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-hydroxyisobutyryl-CoA hydrolase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247880 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hypoxia-inducible factor 1-alpha inhibitor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247881 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Hikeshi levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247882 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homeodomain-interacting protein kinase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 homeodomain-interacting protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020457 GCST90247883 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histatin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histatin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801678 GCST90247884 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histatin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247885 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histo-blood group ABO system transferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 histo-blood group ABO system transferase measurement http://www.ebi.ac.uk/efo/EFO_0801679 GCST90247886 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone acetyltransferase KAT2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247887 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone acetyltransferase type B catalytic subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 histone acetyltransferase type b catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0020452 GCST90247888 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histidine-rich glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 histidine-rich glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008155 GCST90247889 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone acetyltransferase KAT2B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247890 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone H1.2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histone H1.2 measurement http://www.ebi.ac.uk/efo/EFO_0021966 GCST90247891 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase 2C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 histone-lysine N-methyltransferase 2C measurement http://www.ebi.ac.uk/efo/EFO_0801682 GCST90247892 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase 2D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 histone-lysine N-methyltransferase 2D measurement http://www.ebi.ac.uk/efo/EFO_0801683 GCST90247893 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histidine triad nucleotide-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 histidine triad nucleotide-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020450 GCST90247894 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histidine--tRNA ligase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247895 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. HLA class I histocompatibility antigen, alpha chain G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247896 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. HLA class II histocompatibility antigen gamma chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 HLA class II histocompatibility antigen gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0802607 GCST90247897 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. HLA class II histocompatibility antigen, DQ alpha 2 chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 HLA class II histocompatibility antigen, DQ alpha 2 chain measurement http://www.ebi.ac.uk/efo/EFO_0801686 GCST90247898 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. HLA class II histocompatibility antigen, DR beta 3 chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247899 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High mobility group protein 20A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 high mobility group protein 20A measurement http://www.ebi.ac.uk/efo/EFO_0802599 GCST90247900 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High mobility group protein B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 high mobility group protein B1 measurement http://www.ebi.ac.uk/efo/EFO_0020449 GCST90247901 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High mobility group protein B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 high mobility group protein B2 measurement http://www.ebi.ac.uk/efo/EFO_0801676 GCST90247902 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249405 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein S100-A2 measurement http://www.ebi.ac.uk/efo/EFO_0802961 GCST90249406 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249407 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein S100-A5 measurement http://www.ebi.ac.uk/efo/EFO_0801960 GCST90249408 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein S100-A7 measurement http://www.ebi.ac.uk/efo/EFO_0022002 GCST90249409 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-P levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249410 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-Z levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249411 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Solute carrier family 22 member 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 solute carrier family 22 member 16 measurement http://www.ebi.ac.uk/efo/EFO_0802079 GCST90249412 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Solute carrier family 35 member G2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 solute carrier family 35 member G2 measurement http://www.ebi.ac.uk/efo/EFO_0802080 GCST90249413 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Solute carrier family 41 member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 solute carrier family 41 member 2 measurement http://www.ebi.ac.uk/efo/EFO_0803090 GCST90249414 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hydroxyacylglutathione hydrolase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247960 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hydroxyacid oxidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247961 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801697 GCST90247962 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Iduronate 2-sulfatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 iduronate 2-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020461 GCST90247963 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inosine-5-monophosphate dehydrogenase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247964 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inosine-5-monophosphate dehydrogenase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247965 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isoaspartyl peptidase/L-asparaginase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247966 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Islet amyloid polypeptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247967 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inter-alpha-trypsin inhibitor heavy chain H1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 inter-alpha-trypsin inhibitor heavy chain H1 measurement http://www.ebi.ac.uk/efo/EFO_0801705 GCST90247968 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inter-alpha-trypsin inhibitor heavy chain H2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247969 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inter-alpha-trypsin inhibitor heavy chain H3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247970 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inter-alpha-trypsin inhibitor heavy chain H4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 inter-alpha-trypsin inhibitor heavy chain h4 measurement http://www.ebi.ac.uk/efo/EFO_0020481 GCST90247971 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inter-alpha-trypsin inhibitor heavy chain H5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 inter-alpha-trypsin inhibitor heavy chain H5 measurement http://www.ebi.ac.uk/efo/EFO_0801706 GCST90247972 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibin beta A chain:Inhibin beta B chain heterodimer levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 inhibin beta A chain:inhibin beta B chain heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020470 GCST90247973 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibin beta A chain:Inhibin beta C chain heterodimer levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247974 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Exosome complex component RRP43 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249380 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoic acid receptor responder protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 retinoic acid receptor responder protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802004 GCST90249381 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoic acid receptor responder protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 retinoic acid receptor responder protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008274 GCST90249382 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoic acid receptor responder protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 retinoic acid receptor responder protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802005 GCST90249383 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 40S ribosomal protein S10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249384 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 40S ribosomal protein S19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249385 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 40S ribosomal protein S3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 40s ribosomal protein S3 measurement http://www.ebi.ac.uk/efo/EFO_0020117 GCST90249386 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 40S ribosomal protein S3a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 40S ribosomal protein S3a measurement http://www.ebi.ac.uk/efo/EFO_0801333 GCST90249387 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 40S ribosomal protein S4, X isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 40S ribosomal protein S4, X isoform measurement http://www.ebi.ac.uk/efo/EFO_0801334 GCST90249388 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 40S ribosomal protein S5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249389 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 40S ribosomal protein S7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 40s ribosomal protein S7 measurement http://www.ebi.ac.uk/efo/EFO_0020118 GCST90249390 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribosyldihydronicotinamide dehydrogenase [quinone] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249391 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. R-spondin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249392 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. R-spondin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 r-spondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0021878 GCST90249393 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. R-spondin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 R-spondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0022019 GCST90249394 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RNA polymerase-associated protein RTF1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249395 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-transporting protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249396 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RUN and FYVE domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 RUN and FYVE domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803040 GCST90249397 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ribonuclease UK114 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ribonuclease UK114 measurement http://www.ebi.ac.uk/efo/EFO_0802020 GCST90249398 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Relaxin receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 relaxin receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021950 GCST90249399 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249400 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein S100-A11 measurement http://www.ebi.ac.uk/efo/EFO_0801958 GCST90249401 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90249402 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein S100-A13 measurement http://www.ebi.ac.uk/efo/EFO_0801959 GCST90249403 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein S100-A14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249404 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH3 domain-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 SH3 domain-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802063 GCST90249528 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH3 domain-binding glutamic acid-rich-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249529 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH3 domain-binding glutamic acid-rich-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249530 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH3 domain-binding glutamic acid-rich-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249531 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH3 and multiple ankyrin repeat domains protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249532 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sex hormone-binding globulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90249533 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SHC-transforming protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 shc-transforming protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020738 GCST90249534 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine hydroxymethyltransferase, cytosolic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249535 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Short/branched chain specific acyl-CoA dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249536 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sonic hedgehog protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sonic hedgehog protein measurement http://www.ebi.ac.uk/efo/EFO_0020746 GCST90249537 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801372 GCST90249538 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801373 GCST90249539 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801374 GCST90249540 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialate O-acetylesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 sialate O-acetylesterase measurement http://www.ebi.ac.uk/efo/EFO_0803073 GCST90249541 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sialidase-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249542 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Importin subunit alpha-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248087 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Importin subunit beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 importin subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020468 GCST90248088 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol monophosphatase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248089 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol monophosphatase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248090 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inositol monophosphatase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 inositol monophosphatase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801698 GCST90248091 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibitor of growth protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 inhibitor of growth protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020471 GCST90248092 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibitor of growth protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248093 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibin beta B chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248094 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibin beta C chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 inhibin beta C chain measurement http://www.ebi.ac.uk/efo/EFO_0801696 GCST90248095 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibin beta A chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 inhibin beta A chain measurement http://www.ebi.ac.uk/efo/EFO_0020469 GCST90248096 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysophosphatidic acid phosphatase type 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248244 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysosomal acid phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 lysosomal acid phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0801776 GCST90248245 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Largen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein Largen measurement http://www.ebi.ac.uk/efo/EFO_0802952 GCST90248246 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysophosphatidylcholine acyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 lysophosphatidylcholine acyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801775 GCST90248247 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Linker for activation of T-cells family member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 linker for activation of T-cells family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802710 GCST90248248 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Layilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 layilin measurement http://www.ebi.ac.uk/efo/EFO_0020529 GCST90248249 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lipopolysaccharide-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 lipopolysaccharide-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0021894 GCST90248250 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lutropin-choriogonadotropic hormone receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248251 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine carboxyl methyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine carboxyl methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008207 GCST90248252 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lipocalin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lipocalin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802712 GCST90248253 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactase-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lactase-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802681 GCST90248254 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. L-lactate dehydrogenase A chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248255 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. L-lactate dehydrogenase B chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 L-lactate dehydrogenase B chain measurement http://www.ebi.ac.uk/efo/EFO_0020524 GCST90248256 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. L-lactate dehydrogenase C chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 l-lactate dehydrogenase C chain measurement http://www.ebi.ac.uk/efo/EFO_0802680 GCST90248257 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low density lipoprotein receptor adapter protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248258 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 low-density lipoprotein receptor measurement http://www.ebi.ac.uk/efo/EFO_0021937 GCST90248259 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor-related protein 1, soluble levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 low-density lipoprotein receptor-related protein 1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0801772 GCST90248260 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor-related protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248261 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor-related protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248262 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor-related protein 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248263 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor-related protein 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 low-density lipoprotein receptor-related protein 1B measurement http://www.ebi.ac.uk/efo/EFO_0021873 GCST90248264 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor-related protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248265 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor-related protein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 low-density lipoprotein receptor-related protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0020538 GCST90248266 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low-density lipoprotein receptor class A domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248267 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein LDOC1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein LDOC1 measurement http://www.ebi.ac.uk/efo/EFO_0801951 GCST90248268 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Liver-expressed antimicrobial peptide 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248269 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte cell-derived chemotaxin 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leukocyte cell-derived chemotaxin 1 measurement http://www.ebi.ac.uk/efo/EFO_0802704 GCST90248270 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte cell-derived chemotaxin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248271 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein LEG1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248272 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leptin receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90248273 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. LETM1 domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248274 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukosialin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248275 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukotriene A-4 hydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leukotriene a-4 hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020535 GCST90248276 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukotriene B4 receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248277 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte elastase inhibitor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248278 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphocyte function-associated antigen 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 lymphocyte function-associated antigen 3 measurement http://www.ebi.ac.uk/efo/EFO_0802715 GCST90248279 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat LGI family member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine-rich repeat LGI family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802694 GCST90248280 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Legumain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 legumain measurement http://www.ebi.ac.uk/efo/EFO_0020530 GCST90248281 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing G-protein coupled receptor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248282 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing G-protein coupled receptor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248283 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukemia inhibitory factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leukemia inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0801764 GCST90248284 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukemia inhibitory factor receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90248285 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802691 GCST90248286 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802692 GCST90248287 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Four and a half LIM domains protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248288 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. LIM domain and actin-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248289 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein lin-7 homolog A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248290 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein lin-7 homolog B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein lin-7 homolog B measurement http://www.ebi.ac.uk/efo/EFO_0021978 GCST90248291 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein lin-7 homolog C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248292 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Liprin-alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248293 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246877 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 carboxypeptidase e measurement http://www.ebi.ac.uk/efo/EFO_0020234 GCST90246878 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 carboxypeptidase M measurement http://www.ebi.ac.uk/efo/EFO_0801454 GCST90246879 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase N catalytic chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246880 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase N subunit 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246881 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase Q levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246882 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxypeptidase Z levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 carboxypeptidase Z measurement http://www.ebi.ac.uk/efo/EFO_0801455 GCST90246883 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonyl reductase [NADPH] 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246884 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonyl reductase [NADPH] 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246885 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystathionine beta-synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cystathionine beta-synthase measurement http://www.ebi.ac.uk/efo/EFO_0802443 GCST90246886 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chromobox protein homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246887 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chromobox protein homolog 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 chromobox protein homolog 5 measurement http://www.ebi.ac.uk/efo/EFO_0020258 GCST90246888 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome b-c1 complex subunit 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cytochrome b-c1 complex subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0802447 GCST90246889 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement component C8 gamma chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246890 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil domain-containing protein 126 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 coiled-coil domain-containing protein 126 measurement http://www.ebi.ac.uk/efo/EFO_0801482 GCST90246891 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil domain-containing protein 134 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 coiled-coil domain-containing protein 134 measurement http://www.ebi.ac.uk/efo/EFO_0802410 GCST90246892 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil domain-containing protein 167 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 coiled-coil domain-containing protein 167 measurement http://www.ebi.ac.uk/efo/EFO_0802411 GCST90246893 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil domain-containing protein 25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246894 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil domain-containing protein 50 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246895 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil domain-containing protein 51 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 coiled-coil domain-containing protein 51 measurement http://www.ebi.ac.uk/efo/EFO_0802412 GCST90246896 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil domain-containing protein 80 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 coiled-coil domain-containing protein 80 measurement http://www.ebi.ac.uk/efo/EFO_0020268 GCST90246897 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cholecystokinin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246898 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cerebral cavernous malformations 2 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cerebral cavernous malformations 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0802389 GCST90246899 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 C-C motif chemokine 1 measurement http://www.ebi.ac.uk/efo/EFO_0008041 GCST90246900 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020195 GCST90246901 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 C-C motif chemokine 14 measurement http://www.ebi.ac.uk/efo/EFO_0008042 GCST90246902 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90246903 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90246904 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 C-C motif chemokine 17 measurement http://www.ebi.ac.uk/efo/EFO_0008045 GCST90246905 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 C-C motif chemokine 18 measurement http://www.ebi.ac.uk/efo/EFO_0008046 GCST90246906 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 C-C motif chemokine 19 measurement http://www.ebi.ac.uk/efo/EFO_0008047 GCST90246907 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-C motif chemokine 2 measurement http://www.ebi.ac.uk/efo/EFO_0021961 GCST90246908 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 20 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-C motif chemokine 20 measurement http://www.ebi.ac.uk/efo/EFO_0010910 GCST90246909 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 21 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-C motif chemokine 21 measurement http://www.ebi.ac.uk/efo/EFO_0008048 GCST90246910 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 22 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90246911 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90246912 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 24 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 C-C motif chemokine 24 measurement http://www.ebi.ac.uk/efo/EFO_0020197 GCST90246913 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90246914 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-C motif chemokine 27 measurement http://www.ebi.ac.uk/efo/EFO_0020198 GCST90246915 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 28 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 C-C motif chemokine 28 measurement http://www.ebi.ac.uk/efo/EFO_0020199 GCST90246916 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 C-C motif chemokine 3 measurement http://www.ebi.ac.uk/efo/EFO_0008051 GCST90246917 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 3-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 C-C motif chemokine 3-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008052 GCST90246918 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 4-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 C-C motif chemokine 4-like measurement http://www.ebi.ac.uk/efo/EFO_0021848 GCST90246919 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 C-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008053 GCST90246920 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST90246921 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-C motif chemokine 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 C-C motif chemokine 8 measurement http://www.ebi.ac.uk/efo/EFO_0008055 GCST90246922 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase CCNB1IP1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 E3 ubiquitin-protein ligase CCNB1IP1 measurement http://www.ebi.ac.uk/efo/EFO_0802502 GCST90246923 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcipressin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 calcipressin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801442 GCST90246924 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell cycle progression protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cell cycle progression protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802382 GCST90246925 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Copper chaperone for superoxide dismutase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246926 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Procollagen C-endopeptidase enhancer 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 procollagen C-endopeptidase enhancer 2 measurement http://www.ebi.ac.uk/efo/EFO_0801921 GCST90248895 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptide chain release factor 1-like, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peptide chain release factor 1-like, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801870 GCST90248896 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proprotein convertase subtilisin/kexin type 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90248897 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proprotein convertase subtilisin/kexin type 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90248898 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable carboxypeptidase X1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 probable carboxypeptidase X1 measurement http://www.ebi.ac.uk/efo/EFO_0801914 GCST90248899 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prenylcysteine oxidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248900 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prenylcysteine oxidase-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 prenylcysteine oxidase-like measurement http://www.ebi.ac.uk/efo/EFO_0801910 GCST90248901 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Programmed cell death 6-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248902 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Advanced glycosylation end product-specific receptor, soluble levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 advanced glycosylation end product-specific receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0020131 GCST90246455 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arf-GAP domain and FG repeat-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 arf-GAP domain and FG repeat-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803312 GCST90246456 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiogenic factor with G patch and FHA domains 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 angiogenic factor with G patch and FHA domains 1 measurement http://www.ebi.ac.uk/efo/EFO_0802278 GCST90246457 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aggrecan core protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 aggrecan core protein measurement http://www.ebi.ac.uk/efo/EFO_0020133 GCST90246458 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Anterior gradient protein 2 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 anterior gradient protein 2 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020152 GCST90246459 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Anterior gradient protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246460 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Agrin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246461 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Activator of 90 kDa heat shock protein ATPase homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 activator of 90 kDa heat shock protein ATPase homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0801341 GCST90246462 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-hemoglobin-stabilizing protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246463 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Axin interactor, dorsalization-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246464 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apoptosis-inducing factor 1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 apoptosis-inducing factor 1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801389 GCST90246465 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Allograft inflammatory factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 allograft inflammatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020135 GCST90246466 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Allograft inflammatory factor 1-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246467 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-internexin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-internexin measurement http://www.ebi.ac.uk/efo/EFO_0802268 GCST90246468 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AH receptor-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 AH receptor-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0020134 GCST90246469 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldo-keto reductase family 1 member C1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 aldo-keto reductase family 1 member C1 measurement http://www.ebi.ac.uk/efo/EFO_0801363 GCST90246470 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aldo-keto reductase family 1 member C3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246471 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein C-II levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90246547 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein C-III levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246548 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90246549 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90246550 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 apolipoprotein F measurement http://www.ebi.ac.uk/efo/EFO_0801388 GCST90246551 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein L1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90246552 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA dC->dU-editing enzyme APOBEC-3G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DNA dC->dU-editing enzyme APOBEC-3G measurement http://www.ebi.ac.uk/efo/EFO_0802473 GCST90246553 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein L3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246554 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 apolipoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0021945 GCST90246555 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aprataxin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246556 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 2-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246557 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Actin-related protein 2/3 complex subunit 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246558 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amphiregulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 amphiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020144 GCST90246559 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246560 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ADP-ribosylation factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802259 GCST90246561 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246562 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246563 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor GTPase-activating protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246564 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor GTPase-activating protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ADP-ribosylation factor GTPase-activating protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801351 GCST90246565 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arfaptin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 arfaptin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801392 GCST90246566 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arfaptin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 arfaptin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801393 GCST90246567 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arginase-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246568 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arginase-2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246569 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Appetite-regulating hormone levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 appetite-regulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0022016 GCST90246570 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AT-rich interactive domain-containing protein 3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 AT-rich interactive domain-containing protein 3A measurement http://www.ebi.ac.uk/efo/EFO_0020165 GCST90246571 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 annexin A2 measurement http://www.ebi.ac.uk/efo/EFO_0008027 GCST90246522 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246523 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 annexin A5 measurement http://www.ebi.ac.uk/efo/EFO_0021959 GCST90246524 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 annexin A6 measurement http://www.ebi.ac.uk/efo/EFO_0020151 GCST90246525 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246526 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Annexin A8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246527 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AP-1 complex subunit gamma-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246528 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AP-2 complex subunit alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246529 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bis(5-nucleosyl)-tetraphosphatase [asymmetrical] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246530 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AP-4 complex accessory subunit tepsin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 AP-4 complex accessory subunit tepsin measurement http://www.ebi.ac.uk/efo/EFO_0801384 GCST90246531 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amyloid beta A4 precursor protein-binding family B member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 amyloid beta A4 precursor protein-binding family B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802275 GCST90246532 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amyloid beta A4 precursor protein-binding family B member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 amyloid beta A4 precursor protein-binding family B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801379 GCST90246533 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amyloid beta A4 precursor protein-binding family B member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 amyloid beta A4 precursor protein-binding family B member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802276 GCST90246534 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Anaphase-promoting complex subunit 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 anaphase-promoting complex subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0801381 GCST90246535 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein APCDD1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein APCDD1 measurement http://www.ebi.ac.uk/efo/EFO_0802924 GCST90246536 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apelin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246537 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amyloid-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246538 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amyloid-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 amyloid-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801380 GCST90246539 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adipocyte plasma membrane-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 adipocyte plasma membrane-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801348 GCST90246540 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein A-I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246541 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein A-II levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246542 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein A-IV levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 apolipoprotein A-IV measurement http://www.ebi.ac.uk/efo/EFO_0007848 GCST90246543 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein A-V levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 apolipoprotein A-V measurement http://www.ebi.ac.uk/efo/EFO_0801387 GCST90246544 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 10 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90246545 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Apolipoprotein C-I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246546 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of (7Z-10Z-13Z-16Z-19Z)-Docosa-7-10-13-16-19-pentaenoic acid 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267412 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of (R)-S-Lactoylglutathione.1 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267413 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione (reduced); deltaMass: -0.0338 Da] 243 individuals NA NR [811782] (imputed) 2 reduced glutathione measurement http://www.ebi.ac.uk/efo/EFO_0801162 GCST90267414 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione (reduced); deltaMass: -348.1329 Da] 243 individuals NA NR [811782] (imputed) 1 reduced glutathione measurement http://www.ebi.ac.uk/efo/EFO_0801162 GCST90267415 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione (reduced); deltaMass: 0.9383 Da] 243 individuals NA NR [811782] (imputed) 1 reduced glutathione measurement http://www.ebi.ac.uk/efo/EFO_0801162 GCST90267416 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: -0.1044 Da] 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267417 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: -0.1063 Da] 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267418 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: -1.0187 Da] 243 individuals NA NR [811782] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267419 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: 0.7140 Da] 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267420 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: 0.9791 Da] 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267421 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: 130.8002 Da] 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267422 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: 308.8754 Da] 243 individuals NA NR [811782] (imputed) 5 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267423 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: L-Glutathione oxidized; deltaMass: 308.8758 Da] 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267424 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of [Similar to: gamma-Glutamylcysteine; deltaMass: -146.3080 Da] 243 individuals NA NR [811782] (imputed) 7 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267425 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 1-Methylxanthine 243 individuals NA NR [811782] (imputed) 1 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90267426 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 11-HETE.1 243 individuals NA NR [811782] (imputed) 22 HETE measurement http://www.ebi.ac.uk/efo/EFO_0801166 GCST90267427 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 12(13)-DiHOME 243 individuals NA NR [811782] (imputed) 2 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90267428 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 12(13)-EpOME 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267429 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 14-HDoHE.1 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267430 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 15-HETE 243 individuals NA NR [811782] (imputed) 17 HETE measurement http://www.ebi.ac.uk/efo/EFO_0801166 GCST90267431 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 2-Deoxy-alpha-D-glucoside 243 individuals NA NR [811782] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267432 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 2-Hydroxyglutarate (uM) 243 individuals NA NR [811782] (imputed) 1 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90267433 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 2-Hydroxyglutarate/Citramalate 243 individuals NA NR [811782] (imputed) 2 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90267434 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 2-Oxoglutaramate 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267435 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 2S-5S-Methionine sulfoximine 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267436 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ADP-ribosylation factor-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801354 GCST90246572 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ADP-ribosylation factor-like protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0801355 GCST90246573 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246574 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ADP-ribosylation factor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801356 GCST90246575 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 4D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246576 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 5B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246577 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246578 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 8B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246579 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosylation factor-like protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246580 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Argininosuccinate lyase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246581 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Programmed cell death protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248903 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Programmed cell death protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 programmed cell death protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801927 GCST90248904 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Programmed cell death protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248905 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. cGMP-inhibited 3,5-cyclic phosphodiesterase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248906 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. cGMP-specific 3,5-cyclic phosphodiesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248907 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-derived growth factor subunit A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 platelet-derived growth factor subunit A measurement http://www.ebi.ac.uk/efo/EFO_0801890 GCST90248908 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-derived growth factor subunit B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 platelet-derived growth factor subunit b measurement http://www.ebi.ac.uk/efo/EFO_0020650 GCST90248909 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-derived growth factor C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 platelet-derived growth factor c measurement http://www.ebi.ac.uk/efo/EFO_0020648 GCST90248910 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-derived growth factor D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 platelet-derived growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0801888 GCST90248911 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-derived growth factor receptor alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 platelet-derived growth factor receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0021844 GCST90248912 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-derived growth factor receptor beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90248913 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein delta homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein delta homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0801938 GCST90248914 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein delta homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein delta homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0802930 GCST90248915 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein disulfide-isomerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein disulfide-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020669 GCST90248916 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein disulfide-isomerase A3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein disulfide-isomerase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020668 GCST90248917 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 3-Dehydrocarnitine 243 individuals NA NR [811782] (imputed) 1 3-dehydrocarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021037 GCST90267437 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 4-Aminobenzoate 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267438 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 5-6-Dihydrothymine 243 individuals NA NR [811782] (imputed) 4 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90267439 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 5-Deoxyribose-1-phosphate 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267440 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 5(S)-HETE 243 individuals NA NR [811782] (imputed) 3 HETE measurement http://www.ebi.ac.uk/efo/EFO_0801166 GCST90267441 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 8-HETE.1 243 individuals NA NR [811782] (imputed) 1 HETE measurement http://www.ebi.ac.uk/efo/EFO_0801166 GCST90267442 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 9-HETE.1 243 individuals NA NR [811782] (imputed) 1 HETE measurement http://www.ebi.ac.uk/efo/EFO_0801166 GCST90267443 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 9,10-diHOME 243 individuals NA NR [811782] (imputed) 5 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90267444 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of 9,10,EpOME 243 individuals NA NR [811782] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267445 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of AA 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267446 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of acetyl-carnitine 243 individuals NA NR [811782] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90267447 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of acyl-C18:2 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267448 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of ADP 243 individuals NA NR [811782] (imputed) 3 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90267449 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of ADP-D-ribose 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267450 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Allantoate 243 individuals NA NR [811782] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267451 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Arachidonic Acid 243 individuals NA NR [811782] (imputed) 2 arachidonic acid measurement http://www.ebi.ac.uk/efo/EFO_0006808 GCST90267452 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Arg (uM) 243 individuals NA NR [811782] (imputed) 2 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90267453 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Asp (uM) 243 individuals NA NR [811782] (imputed) 1 aspartic acid measurement http://www.ebi.ac.uk/efo/EFO_0801113 GCST90267454 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of ATP (consider breakdown) (uM) 243 individuals NA NR [811782] (imputed) 1 ATP measurement http://www.ebi.ac.uk/efo/EFO_0801116 GCST90267455 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Biliverdin 243 individuals NA NR [811782] (imputed) 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90267456 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Biliverdin.1 243 individuals NA NR [811782] (imputed) 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90267457 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Bisphenol A 243 individuals NA NR [811782] (imputed) 1 bisphenol A measurement http://www.ebi.ac.uk/efo/EFO_0801079 GCST90267458 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Butanoic acid 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267459 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of Choline 243 individuals NA NR [811782] (imputed) 1 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90267460 Genome-wide genotyping array 2023-04-14 36395887 Moore A 2022-11-14 J Biol Chem www.ncbi.nlm.nih.gov/pubmed/36395887 Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. RBC levels of cis-p-Coumarate 243 individuals NA NR [811782] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90267461 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth arrest-specific protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 growth arrest-specific protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020425 GCST90247686 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth arrest-specific protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247687 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gastrin-releasing peptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 gastrin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0022000 GCST90247688 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gastrokine-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247689 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gastrokine-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247690 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gastrotropin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247691 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycine amidinotransferase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247692 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247693 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-T2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-T2 measurement http://www.ebi.ac.uk/efo/EFO_0802588 GCST90247694 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanylate-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247695 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanylate-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247696 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanylate-binding protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 guanylate-binding protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801662 GCST90247697 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTP cyclohydrolase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247698 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucokinase regulatory protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glucokinase regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0020406 GCST90247699 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutamate--cysteine ligase regulatory subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247700 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 measurement http://www.ebi.ac.uk/efo/EFO_0801407 GCST90247701 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutamate carboxypeptidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90247702 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granulocyte colony-stimulating factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90247703 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granulocyte colony-stimulating factor receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 granulocyte colony-stimulating factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020416 GCST90247704 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycine cleavage system H protein, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247705 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pleckstrin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249031 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802912 GCST90249032 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802913 GCST90249033 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Patatin-like phospholipase domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249034 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyridoxal phosphate phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pyridoxal phosphate phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0020694 GCST90249035 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 107 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 107 measurement http://www.ebi.ac.uk/efo/EFO_0802317 GCST90246669 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 108B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 108B measurement http://www.ebi.ac.uk/efo/EFO_0802318 GCST90246670 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-defensin 110 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-defensin 110 measurement http://www.ebi.ac.uk/efo/EFO_0802319 GCST90246671 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. G antigen 2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247664 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycosaminoglycan xylosylkinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 glycosaminoglycan xylosylkinase measurement http://www.ebi.ac.uk/efo/EFO_0801647 GCST90247665 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galactoside 3(4)-L-fucosyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247666 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galanin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247667 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 galectin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020932 GCST90247668 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 galectin-10 measurement http://www.ebi.ac.uk/efo/EFO_0021918 GCST90247669 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 galectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020397 GCST90247670 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90247671 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-3-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 galectin-3-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010241 GCST90247672 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 galectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020398 GCST90247673 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 galectin-7 measurement http://www.ebi.ac.uk/efo/EFO_0022034 GCST90247674 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 galectin-8 measurement http://www.ebi.ac.uk/efo/EFO_0020399 GCST90247675 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 galectin-9 measurement http://www.ebi.ac.uk/efo/EFO_0021863 GCST90247676 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galectin-related protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247677 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0801611 GCST90247678 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galactokinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247679 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galactoside-binding soluble lectin 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247680 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galactosylceramide sulfotransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247681 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-crystallin D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 gamma-crystallin D measurement http://www.ebi.ac.uk/efo/EFO_0802560 GCST90247682 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-enolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 gamma-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021845 GCST90247683 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gap junction delta-2 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 gap junction delta-2 protein measurement http://www.ebi.ac.uk/efo/EFO_0802562 GCST90247684 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Golgi-associated plant pathogenesis-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247685 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246774 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C3b, inactivated levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 complement C3B, inactivated measurement http://www.ebi.ac.uk/efo/EFO_0020276 GCST90246778 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C3d fragment levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement C3D fragment measurement http://www.ebi.ac.uk/efo/EFO_0020277 GCST90246779 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C4b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 complement C4b measurement http://www.ebi.ac.uk/efo/EFO_0008092 GCST90246783 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C4b-binding protein beta chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246785 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C5a anaphylatoxin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 C5a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020208 GCST90246788 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C5b-C6 complex levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 complement C5B-C6 complex measurement http://www.ebi.ac.uk/efo/EFO_0020279 GCST90246789 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytosolic 5-nucleotidase 3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246790 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement component C6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 complement component C6 measurement http://www.ebi.ac.uk/efo/EFO_0020281 GCST90246792 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement component C8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 complement component C8 measurement http://www.ebi.ac.uk/efo/EFO_0008094 GCST90246794 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement component C9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90246795 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CD99 antigen-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246796 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-binding protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246797 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-binding protein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 calcium-binding protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802357 GCST90246798 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytoplasmic tyrosine-protein kinase BMX levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cytoplasmic tyrosine-protein kinase BMX measurement http://www.ebi.ac.uk/efo/EFO_0020308 GCST90246724 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802304 GCST90246725 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Brain natriuretic peptide 32 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 brain natriuretic peptide 32 measurement http://www.ebi.ac.uk/efo/EFO_0020191 GCST90246726 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Brother of CDO levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 brother of CDO measurement http://www.ebi.ac.uk/efo/EFO_0020194 GCST90246727 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BolA-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246728 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BolA-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 bolA-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802335 GCST90246729 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BolA-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246730 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bactericidal permeability-increasing protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 bactericidal permeability-increasing protein measurement http://www.ebi.ac.uk/efo/EFO_0020172 GCST90246731 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BPI fold-containing family A member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 BPI fold-containing family A member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802336 GCST90246732 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BPI fold-containing family A member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246733 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BPI fold-containing family B member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 BPI fold-containing family B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0801429 GCST90246734 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3(2),5-bisphosphate nucleotidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246735 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BRCA1-A complex subunit Abraxas levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246736 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BRCA2 and CDKN1A-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246737 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bromodomain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 bromodomain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801431 GCST90246738 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bromodomain testis-specific protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 bromodomain testis-specific protein measurement http://www.ebi.ac.uk/efo/EFO_0802339 GCST90246739 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Brevican core protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 brevican core protein measurement http://www.ebi.ac.uk/efo/EFO_0020193 GCST90246740 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BRICHOS domain-containing protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 BRICHOS domain-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801430 GCST90246741 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BRISC complex subunit Abro1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 BRISC complex subunit Abro1 measurement http://www.ebi.ac.uk/efo/EFO_0802338 GCST90246742 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Brorin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 brorin measurement http://www.ebi.ac.uk/efo/EFO_0801432 GCST90246743 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-soluble NSF attachment protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-soluble NSF attachment protein measurement http://www.ebi.ac.uk/efo/EFO_0801423 GCST90246744 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone sialoprotein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 bone sialoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020190 GCST90246745 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Brain-specific serine protease 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 brain-specific serine protease 4 measurement http://www.ebi.ac.uk/efo/EFO_0020192 GCST90246746 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90246747 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone marrow stromal antigen 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246748 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Baculoviral IAP repeat-containing protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 baculoviral IAP repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020174 GCST90246699 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Baculoviral IAP repeat-containing protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246700 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Baculoviral IAP repeat-containing protein 7 Isoform beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 baculoviral IAP repeat-containing protein 7 isoform beta measurement http://www.ebi.ac.uk/efo/EFO_0020175 GCST90246701 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bile acid receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246702 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bile salt-activated lipase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 bile salt-activated lipase measurement http://www.ebi.ac.uk/efo/EFO_0801425 GCST90246703 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bile salt sulfotransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 bile salt sulfotransferase measurement http://www.ebi.ac.uk/efo/EFO_0802333 GCST90246704 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Biotinidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246705 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-klotho levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246706 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bleomycin hydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246707 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Biogenesis of lysosome-related organelles complex 1 subunit 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246708 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-mannosidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 beta-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801421 GCST90246709 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B melanoma antigen 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 B melanoma antigen 2 measurement http://www.ebi.ac.uk/efo/EFO_0801401 GCST90246710 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. B melanoma antigen 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 b melanoma antigen 3 measurement http://www.ebi.ac.uk/efo/EFO_0802299 GCST90246711 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-microseminoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 beta-microseminoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020955 GCST90246712 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone marrow proteoglycan levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246713 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein receptor type-1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246714 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 bone morphogenetic protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020185 GCST90246715 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246716 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246717 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246718 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246719 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90246720 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 bone morphogenetic protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020187 GCST90246721 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bone morphogenetic protein 8B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246722 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. BMP-binding endothelial regulator protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 BMP-binding endothelial regulator protein measurement http://www.ebi.ac.uk/efo/EFO_0020183 GCST90246723 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90246775 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C3a anaphylatoxin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C3a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020207 GCST90246776 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C3b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement C3B measurement http://www.ebi.ac.uk/efo/EFO_0020275 GCST90246777 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST90246780 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen type IV alpha-3-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246781 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C4a anaphylatoxin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246782 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C4b-binding protein alpha chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246784 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement C5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246786 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome b561 domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246787 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutaredoxin-like protein C5orf63 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glutaredoxin-like protein C5orf63 measurement http://www.ebi.ac.uk/efo/EFO_0801634 GCST90246791 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement component C7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90246793 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-type tyrosine-protein phosphatase U levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 receptor-type tyrosine-protein phosphatase U measurement http://www.ebi.ac.uk/efo/EFO_0803002 GCST90249182 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phenylalanine--tRNA ligase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 phenylalanine--tRNA ligase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801879 GCST90249183 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pro-Thyrotropin-releasing hormone levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249184 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein-tyrosine sulfotransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein-tyrosine sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801970 GCST90249185 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein-tyrosine sulfotransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein-tyrosine sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801971 GCST90249186 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pentraxin-related protein PTX3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 pentraxin-related protein PTX3 measurement http://www.ebi.ac.uk/efo/EFO_0010923 GCST90249187 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenylosuccinate synthetase isozyme 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 adenylosuccinate synthetase isozyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0802256 GCST90249188 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenylosuccinate synthetase isozyme 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 adenylosuccinate synthetase isozyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0801345 GCST90249189 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Potassium voltage-gated channel subfamily A member 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 potassium voltage-gated channel subfamily A member 10 measurement http://www.ebi.ac.uk/efo/EFO_0802888 GCST90249190 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Potassium voltage-gated channel subfamily E regulatory beta subunit 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 potassium voltage-gated channel subfamily E regulatory beta subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0801902 GCST90249191 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Potassium voltage-gated channel subfamily F member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 potassium voltage-gated channel subfamily F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0802890 GCST90249192 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Potassium voltage-gated channel subfamily G member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 potassium voltage-gated channel subfamily G member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802891 GCST90249193 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249194 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plexin domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249195 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peroxidasin homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249196 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Peptide YY levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 peptide yy measurement http://www.ebi.ac.uk/efo/EFO_0020623 GCST90249197 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Z-dependent protease inhibitor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90249198 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pregnancy zone protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249199 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Quinone oxidoreductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249200 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Quinone oxidoreductase-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 quinone oxidoreductase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021880 GCST90249201 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Quinone oxidoreductase PIG3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249202 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rap1 GTPase-GDP dissociation stimulator 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 rap1 GTPase-GDP dissociation stimulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0802990 GCST90249203 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. rRNA 2-O-methyltransferase fibrillarin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249204 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Reticulon-4-interacting protein 1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249205 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Reticulon-4 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90249206 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Granzyme M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 granzyme M measurement http://www.ebi.ac.uk/efo/EFO_0801655 GCST90247806 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GRB2-related adapter protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 GRB2-related adapter protein measurement http://www.ebi.ac.uk/efo/EFO_0802580 GCST90247807 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GRB2-related adapter protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90247808 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth factor receptor-bound protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247809 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth factor receptor-bound protein 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 growth factor receptor-bound protein 14 measurement http://www.ebi.ac.uk/efo/EFO_0801658 GCST90247810 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth factor receptor-bound protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 growth factor receptor-bound protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0801659 GCST90247811 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gremlin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 gremlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020421 GCST90247812 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gremlin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 gremlin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801656 GCST90247813 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutamate receptor ionotropic, delta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glutamate receptor ionotropic, delta-2 measurement http://www.ebi.ac.uk/efo/EFO_0801631 GCST90247814 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GRAM domain-containing protein 1C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 GRAM domain-containing protein 1C measurement http://www.ebi.ac.uk/efo/EFO_0801652 GCST90247815 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth-regulated alpha protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST90247816 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gro-beta/gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 gro-beta/gamma measurement http://www.ebi.ac.uk/efo/EFO_0020422 GCST90247817 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GrpE protein homolog 1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 grpE protein homolog 1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802581 GCST90247818 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione synthetase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247819 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycogen synthase kinase-3 alpha/beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glycogen synthase kinase-3 alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020412 GCST90247820 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GSK3-beta interaction protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 GSK3-beta interaction protein measurement http://www.ebi.ac.uk/efo/EFO_0802582 GCST90247821 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 glutathione S-transferase A1 measurement http://www.ebi.ac.uk/efo/EFO_0801636 GCST90247822 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase A4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glutathione S-transferase A4 measurement http://www.ebi.ac.uk/efo/EFO_0801637 GCST90247823 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutathione S-transferase theta-2B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 glutathione S-transferase theta-2B measurement http://www.ebi.ac.uk/efo/EFO_0802572 GCST90247824 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. General transcription factor II-I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 general transcription factor II-I measurement http://www.ebi.ac.uk/efo/EFO_0801623 GCST90247825 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTP-binding protein Di-Ras1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247826 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTP-binding protein Di-Ras3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 GTP-binding protein Di-Ras3 measurement http://www.ebi.ac.uk/efo/EFO_0802584 GCST90247827 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTP-binding protein GEM levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 GTP-binding protein GEM measurement http://www.ebi.ac.uk/efo/EFO_0801660 GCST90247828 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTP-binding nuclear protein Ran levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 GTP-binding nuclear protein ran measurement http://www.ebi.ac.uk/efo/EFO_0020431 GCST90247829 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. GTP-binding protein SAR1a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247830 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanine deaminase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 guanine deaminase measurement http://www.ebi.ac.uk/efo/EFO_0802585 GCST90247831 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Guanine nucleotide exchange factor DBS levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 guanine nucleotide exchange factor DBS measurement http://www.ebi.ac.uk/efo/EFO_0802586 GCST90247832 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome activator complex subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90249159 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome activator complex subunit 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 proteasome activator complex subunit 3 measurement http://www.ebi.ac.uk/efo/EFO_0020662 GCST90249160 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasome assembly chaperone 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 proteasome assembly chaperone 3 measurement http://www.ebi.ac.uk/efo/EFO_0802921 GCST90249161 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostate-associated microseminoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 prostate-associated microseminoprotein measurement http://www.ebi.ac.uk/efo/EFO_0802920 GCST90249162 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pulmonary surfactant-associated protein B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249163 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pulmonary surfactant-associated protein D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90249164 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylcholine-sterol acyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249165 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein PET117 homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249166 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PTB domain-containing engulfment adapter protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249167 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase pten measurement http://www.ebi.ac.uk/efo/EFO_0020635 GCST90249168 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostaglandin reductase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 prostaglandin reductase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801932 GCST90249169 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostaglandin reductase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249170 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostaglandin reductase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249171 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Parathyroid hormone levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST90249172 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Parathyroid hormone-related protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 parathyroid hormone-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020622 GCST90249173 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protachykinin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protachykinin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801934 GCST90249174 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein-tyrosine kinase 2-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein-tyrosine kinase 2-beta measurement http://www.ebi.ac.uk/efo/EFO_0801969 GCST90249175 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein-tyrosine kinase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein-tyrosine kinase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020691 GCST90249176 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pleiotrophin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pleiotrophin measurement http://www.ebi.ac.uk/efo/EFO_0020651 GCST90249177 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-type tyrosine-protein phosphatase eta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 receptor-type tyrosine-protein phosphatase eta measurement http://www.ebi.ac.uk/efo/EFO_0802999 GCST90249178 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-type tyrosine-protein phosphatase H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 receptor-type tyrosine-protein phosphatase H measurement http://www.ebi.ac.uk/efo/EFO_0801991 GCST90249179 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-type tyrosine-protein phosphatase R levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 receptor-type tyrosine-protein phosphatase R measurement http://www.ebi.ac.uk/efo/EFO_0803000 GCST90249180 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-type tyrosine-protein phosphatase S levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 receptor-type tyrosine-protein phosphatase S measurement http://www.ebi.ac.uk/efo/EFO_0803001 GCST90249181 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. High mobility group protein B3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 high mobility group protein B3 measurement http://www.ebi.ac.uk/efo/EFO_0801677 GCST90247903 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho GTPase-activating protein 45 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247904 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kininogen, HMW, Two Chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247905 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hematological and neurological expressed 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247906 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hepatocyte nuclear factor 4-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 hepatocyte nuclear factor 4-alpha measurement http://www.ebi.ac.uk/efo/EFO_0801672 GCST90247907 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein A/B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 heterogeneous nuclear ribonucleoprotein a/b measurement http://www.ebi.ac.uk/efo/EFO_0020441 GCST90247908 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoproteins A2/B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 heterogeneous nuclear ribonucleoproteins A2/B1 measurement http://www.ebi.ac.uk/efo/EFO_0020444 GCST90247909 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoproteins C1/C2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 heterogeneous nuclear ribonucleoproteins C1/C2 measurement http://www.ebi.ac.uk/efo/EFO_0801675 GCST90247910 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247911 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein D0 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247912 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein D-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 heterogeneous nuclear ribonucleoprotein D-like measurement http://www.ebi.ac.uk/efo/EFO_0801673 GCST90247913 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247914 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247915 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 heterogeneous nuclear ribonucleoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0801674 GCST90247916 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein Q levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 heterogeneous nuclear ribonucleoprotein q measurement http://www.ebi.ac.uk/efo/EFO_0020443 GCST90247917 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heterogeneous nuclear ribonucleoprotein R levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247918 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heme oxygenase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247919 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 4-hydroxy-2-oxoglutarate aldolase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 4-hydroxy-2-oxoglutarate aldolase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802240 GCST90247920 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Holo-Transcobalamin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247921 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homeodomain-only protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247922 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hippocalcin-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247923 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hematopoietic prostaglandin D synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 hematopoietic prostaglandin D synthase measurement http://www.ebi.ac.uk/efo/EFO_0801668 GCST90247924 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hephaestin-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 hephaestin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802597 GCST90247925 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hyaluronan and proteoglycan link protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 hyaluronan and proteoglycan link protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020459 GCST90247926 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hyaluronan and proteoglycan link protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247927 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Basement membrane-specific heparan sulfate proteoglycan core protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247953 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease HTRA1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247954 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hexokinase-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247955 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hexokinase-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247956 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hexokinase-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247957 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hyaluronidase-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 hyaluronidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0802612 GCST90247958 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247959 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Retinoschisin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 retinoschisin measurement http://www.ebi.ac.uk/efo/EFO_0803014 GCST90249287 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,3-N-acetylglucosaminyltransferase radical fringe levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 beta-1,3-N-acetylglucosaminyltransferase radical fringe measurement http://www.ebi.ac.uk/efo/EFO_0801408 GCST90249288 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulatory factor X-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 regulatory factor X-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801999 GCST90249289 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras GTPase-activating protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ras GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020698 GCST90249290 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras GTPase-activating protein-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249291 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ras GTPase-activating protein-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249292 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Repulsive guidance molecule A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 repulsive guidance molecule A measurement http://www.ebi.ac.uk/efo/EFO_0008273 GCST90249293 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. RGM domain family member B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 rgm domain family member b measurement http://www.ebi.ac.uk/efo/EFO_0020708 GCST90249294 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho guanine nucleotide exchange factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 rho guanine nucleotide exchange factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802013 GCST90249295 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho guanine nucleotide exchange factor 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 rho guanine nucleotide exchange factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0802014 GCST90249296 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho guanine nucleotide exchange factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 rho guanine nucleotide exchange factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0803018 GCST90249297 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho guanine nucleotide exchange factor 25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 rho guanine nucleotide exchange factor 25 measurement http://www.ebi.ac.uk/efo/EFO_0803019 GCST90249298 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Rho guanine nucleotide exchange factor 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 rho guanine nucleotide exchange factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0803020 GCST90249299 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Redox-regulatory protein FAM213A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 redox-regulatory protein FAM213A measurement http://www.ebi.ac.uk/efo/EFO_0801993 GCST90249300 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249301 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 regulator of G-protein signaling 18 measurement http://www.ebi.ac.uk/efo/EFO_0801995 GCST90249302 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 regulator of G-protein signaling 19 measurement http://www.ebi.ac.uk/efo/EFO_0801996 GCST90249303 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Regulator of G-protein signaling 21 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249304 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homer protein homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247928 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homer protein homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247929 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparanase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247930 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Haptoglobin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90247931 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. HRAS-like suppressor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 HRAS-like suppressor 3 measurement http://www.ebi.ac.uk/efo/EFO_0802611 GCST90247932 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Activator of apoptosis harakiri levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 activator of apoptosis harakiri measurement http://www.ebi.ac.uk/efo/EFO_0802253 GCST90247933 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparan-sulfate 6-O-sulfotransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 heparan-sulfate 6-o-sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020437 GCST90247934 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparan-sulfate 6-O-sulfotransferase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247935 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock 70 kDa protein 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247936 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock 70 kDa protein 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90247937 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock 70 kDa protein 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247938 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock 70 kDa protein 1-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 heat shock 70 kDa protein 1-like measurement http://www.ebi.ac.uk/efo/EFO_0801665 GCST90247939 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock 70 kDa protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 heat shock 70 kDa protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801666 GCST90247940 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock protein HSP 90-alpha/beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 heat shock protein hsp 90-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020435 GCST90247941 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock protein HSP 90-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 heat shock protein HSP 90-beta measurement http://www.ebi.ac.uk/efo/EFO_0021991 GCST90247942 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock protein beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 heat shock protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0010595 GCST90247943 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Hsc70-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247944 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock cognate 71 kDa protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 heat shock cognate 71 kda protein measurement http://www.ebi.ac.uk/efo/EFO_0020434 GCST90247945 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heat shock factor protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247946 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparan sulfate glucosamine 3-O-sulfotransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247947 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparan sulfate glucosamine 3-O-sulfotransferase 3A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 heparan sulfate glucosamine 3-O-sulfotransferase 3A1 measurement http://www.ebi.ac.uk/efo/EFO_0801671 GCST90247948 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparan sulfate glucosamine 3-O-sulfotransferase 3B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 heparan sulfate glucosamine 3-O-sulfotransferase 3B1 measurement http://www.ebi.ac.uk/efo/EFO_0802592 GCST90247949 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparan sulfate glucosamine 3-O-sulfotransferase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 heparan sulfate glucosamine 3-O-sulfotransferase 4 measurement http://www.ebi.ac.uk/efo/EFO_0802593 GCST90247950 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Heparan sulfate glucosamine 3-O-sulfotransferase 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247951 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. HSP 70 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 11 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247952 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon lambda receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interferon lambda receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802646 GCST90248000 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248001 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 immunoglobulin-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801691 GCST90248002 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 immunoglobulin D measurement http://www.ebi.ac.uk/efo/EFO_0020463 GCST90248003 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin superfamily DCC subclass member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 immunoglobulin superfamily DCC subclass member 3 measurement http://www.ebi.ac.uk/efo/EFO_0801689 GCST90248004 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin superfamily DCC subclass member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 immunoglobulin superfamily DCC subclass member 4 measurement http://www.ebi.ac.uk/efo/EFO_0801690 GCST90248005 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 immunoglobulin E measurement http://www.ebi.ac.uk/efo/EFO_0020464 GCST90248006 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like growth factor I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 insulin-like growth factor I measurement http://www.ebi.ac.uk/efo/EFO_0801702 GCST90248007 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like growth factor 1 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 insulin-like growth factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020473 GCST90248008 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like growth factor-binding protein complex acid labile subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248009 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like growth factor-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90248010 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like growth factor-binding protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 insulin-like growth factor-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801703 GCST90248011 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like growth factor-binding protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90248012 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. IGF-like family receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 IGF-like family receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801687 GCST90248013 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin growth factor-like family member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 insulin growth factor-like family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0801700 GCST90248014 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 immunoglobulin G measurement http://www.ebi.ac.uk/efo/EFO_0020465 GCST90248015 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ig gamma-2, Kappa levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ig gamma-2, Kappa measurement http://www.ebi.ac.uk/efo/EFO_0802616 GCST90248016 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive gamma-glutamyltranspeptidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 inactive gamma-glutamyltranspeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801692 GCST90248017 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ig Kappa chain V-I region HK102- like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 ig Kappa chain V-I region HK102- like measurement http://www.ebi.ac.uk/efo/EFO_0802617 GCST90248018 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin lambda-like polypeptide 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 12 immunoglobulin lambda-like polypeptide 1 measurement http://www.ebi.ac.uk/efo/EFO_0801688 GCST90248019 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 immunoglobulin M measurement http://www.ebi.ac.uk/efo/EFO_0020466 GCST90248020 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin superfamily member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248021 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-like growth factor-binding protein-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 insulin-like growth factor-binding protein-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0802631 GCST90247975 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isovaleryl-CoA dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247976 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ICOS ligand levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90247977 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Indoleamine 2,3-dioxygenase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 indoleamine 2,3-dioxygenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801695 GCST90247978 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Insulin-degrading enzyme levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 insulin-degrading enzyme measurement http://www.ebi.ac.uk/efo/EFO_0020472 GCST90247979 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isocitrate dehydrogenase [NADP] cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247980 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247981 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isopentenyl-diphosphate Delta-isomerase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247982 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isopentenyl-diphosphate delta-isomerase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247983 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive dipeptidyl peptidase 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 inactive dipeptidyl peptidase 10 measurement http://www.ebi.ac.uk/efo/EFO_0802624 GCST90247984 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-L-iduronidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90247985 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon-induced protein with tetratricopeptide repeats 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interferon-induced protein with tetratricopeptide repeats 2 measurement http://www.ebi.ac.uk/efo/EFO_0802651 GCST90247986 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon-induced protein with tetratricopeptide repeats 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interferon-induced protein with tetratricopeptide repeats 3 measurement http://www.ebi.ac.uk/efo/EFO_0801710 GCST90247987 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon lambda-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interferon lambda-1 measurement http://www.ebi.ac.uk/efo/EFO_0020485 GCST90247988 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon lambda-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interferon lambda-2 measurement http://www.ebi.ac.uk/efo/EFO_0020486 GCST90247989 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon lambda-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247990 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon alpha/beta receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interferon alpha/beta receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021850 GCST90247991 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon alpha-16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247992 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interferon alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020483 GCST90247993 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon alpha-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interferon alpha-4 measurement http://www.ebi.ac.uk/efo/EFO_0802641 GCST90247994 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon alpha-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interferon alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802642 GCST90247995 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon alpha-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 interferon alpha-7 measurement http://www.ebi.ac.uk/efo/EFO_0021947 GCST90247996 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90247997 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon gamma receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 interferon gamma receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020484 GCST90247998 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon gamma receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90247999 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Immunoglobulin superfamily member 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 immunoglobulin superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0802622 GCST90248022 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Intracellular hyaluronan-binding protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248023 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Indian hedgehog protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248024 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serglycin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249503 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serotransferrin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020735 GCST90249504 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein SET levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein set measurement http://www.ebi.ac.uk/efo/EFO_0020688 GCST90249505 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Set1/Ash2 histone methyltransferase complex subunit ASH2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 set1/Ash2 histone methyltransferase complex subunit ASH2 measurement http://www.ebi.ac.uk/efo/EFO_0803069 GCST90249506 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase SETD2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 histone-lysine N-methyltransferase SETD2 measurement http://www.ebi.ac.uk/efo/EFO_0802604 GCST90249507 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase SETMAR levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 histone-lysine N-methyltransferase SETMAR measurement http://www.ebi.ac.uk/efo/EFO_0802605 GCST90249508 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Splicing factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 splicing factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802085 GCST90249509 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secretoglobin family 3A member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249510 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Splicing factor 3B subunit 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 splicing factor 3B subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0803100 GCST90249511 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Splicing factor 45 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249512 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. S-formylglutathione hydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 S-formylglutathione hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0008275 GCST90249513 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secreted frizzled-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 secreted frizzled-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020718 GCST90249514 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secreted frizzled-related protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 secreted frizzled-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802039 GCST90249515 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secreted frizzled-related protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90249516 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secreted frizzled-related protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249517 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Surfactant-associated protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249518 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sideroflexin-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249519 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sperm-associated antigen 11A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sperm-associated antigen 11A measurement http://www.ebi.ac.uk/efo/EFO_0802082 GCST90249520 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sperm-associated antigen 11B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sperm-associated antigen 11B measurement http://www.ebi.ac.uk/efo/EFO_0803098 GCST90249521 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SAGA-associated factor 29 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 SAGA-associated factor 29 homolog measurement http://www.ebi.ac.uk/efo/EFO_0803042 GCST90249522 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small glutamine-rich tetratricopeptide repeat-containing protein alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 small glutamine-rich tetratricopeptide repeat-containing protein alpha measurement http://www.ebi.ac.uk/efo/EFO_0020744 GCST90249523 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small glutamine-rich tetratricopeptide repeat-containing protein beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249524 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH2 domain-containing protein 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 sh2 domain-containing protein 1a measurement http://www.ebi.ac.uk/efo/EFO_0020737 GCST90249525 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH2 domain-containing protein 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249526 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SH2 domain-containing protein 3C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249527 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secreted and transmembrane protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 secreted and transmembrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021852 GCST90249478 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Selenoprotein H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249479 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Selenoprotein M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249480 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Selenoprotein S levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 selenoprotein S measurement http://www.ebi.ac.uk/efo/EFO_0802046 GCST90249481 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Selenoprotein W levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249482 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related measurement http://www.ebi.ac.uk/efo/EFO_0803114 GCST90249483 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90249484 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-3C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 semaphorin-3C measurement http://www.ebi.ac.uk/efo/EFO_0802048 GCST90249485 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-3E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90249486 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-3G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 semaphorin-3G measurement http://www.ebi.ac.uk/efo/EFO_0802049 GCST90249487 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-4A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249488 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-4C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 semaphorin-4C measurement http://www.ebi.ac.uk/efo/EFO_0803050 GCST90249489 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-4D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 semaphorin-4D measurement http://www.ebi.ac.uk/efo/EFO_0802050 GCST90249490 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-4F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249491 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-5A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 semaphorin-5A measurement http://www.ebi.ac.uk/efo/EFO_0021864 GCST90249492 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-6A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90249493 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-6B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 semaphorin-6B measurement http://www.ebi.ac.uk/efo/EFO_0021885 GCST90249494 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-6C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 semaphorin-6C measurement http://www.ebi.ac.uk/efo/EFO_0803051 GCST90249495 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semaphorin-7A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 semaphorin-7A measurement http://www.ebi.ac.uk/efo/EFO_0803052 GCST90249496 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Semenogelin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 semenogelin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802051 GCST90249497 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sentrin-specific protease 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sentrin-specific protease 7 measurement http://www.ebi.ac.uk/efo/EFO_0803053 GCST90249498 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Septin-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 septin-10 measurement http://www.ebi.ac.uk/efo/EFO_0802053 GCST90249499 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Septin-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249500 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Septin-6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249501 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small EDRK-rich factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249502 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorting nexin-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sorting nexin-7 measurement http://www.ebi.ac.uk/efo/EFO_0803094 GCST90249601 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorting nexin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 sorting nexin-8 measurement http://www.ebi.ac.uk/efo/EFO_0803095 GCST90249602 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Suppressor of cytokine signaling 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 suppressor of cytokine signaling 3 measurement http://www.ebi.ac.uk/efo/EFO_0802104 GCST90249603 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Suppressor of cytokine signaling 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 suppressor of cytokine signaling 7 measurement http://www.ebi.ac.uk/efo/EFO_0803109 GCST90249604 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorcin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249605 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sclerostin domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249606 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sclerostin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 sclerostin measurement http://www.ebi.ac.uk/efo/EFO_0010606 GCST90249607 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin A11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249608 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin A12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 serpin A12 measurement http://www.ebi.ac.uk/efo/EFO_0802061 GCST90249609 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Secretory phospholipase A2 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 secretory phospholipase A2 receptor measurement http://www.ebi.ac.uk/efo/EFO_0802043 GCST90249610 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin A9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 serpin A9 measurement http://www.ebi.ac.uk/efo/EFO_0802062 GCST90249611 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serum paraoxonase/arylesterase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serum paraoxonase/arylesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020736 GCST90249612 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SPARC-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90249613 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium/potassium-transporting ATPase subunit beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249614 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium/potassium-transporting ATPase subunit beta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sodium/potassium-transporting ATPase subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0802078 GCST90249615 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sodium/potassium-transporting ATPase subunit beta-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249616 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Spermatogenesis-associated protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 spermatogenesis-associated protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0803099 GCST90249617 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin B13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249618 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin B5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249619 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serpin B8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249620 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SAM pointed domain-containing Ets transcription factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249621 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease 27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 serine protease 27 measurement http://www.ebi.ac.uk/efo/EFO_0008280 GCST90249622 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine protease 57 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249623 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sperm flagellar protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249624 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acrosomal protein SP-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249625 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. S-methyl-5-thioadenosine phosphorylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249576 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stromal membrane-associated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 stromal membrane-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802094 GCST90249577 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Structural maintenance of chromosomes protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 structural maintenance of chromosomes protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802096 GCST90249578 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small nuclear ribonucleoprotein Sm D2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249579 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small nuclear ribonucleoprotein Sm D3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249580 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SAYSvFN domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 SAYSvFN domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803043 GCST90249581 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SPARC-related modular calcium-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 sPARC-related modular calcium-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021868 GCST90249582 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SPARC-related modular calcium-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249583 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SWI/SNF complex subunit SMARCC1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249584 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Smoothelin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249585 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase SMURF1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249586 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase SMURF2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249587 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-soluble NSF attachment protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-soluble NSF attachment protein measurement http://www.ebi.ac.uk/efo/EFO_0020140 GCST90249588 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptogyrin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249589 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stannin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249590 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stanniocalcin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 stanniocalcin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020753 GCST90249591 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptosomal-associated protein 25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 synaptosomal-associated protein 25 measurement http://www.ebi.ac.uk/efo/EFO_0021858 GCST90249592 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Synaptosomal-associated protein 29 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 synaptosomal-associated protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0803116 GCST90249593 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaphilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249594 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small nuclear ribonucleoprotein F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 small nuclear ribonucleoprotein F measurement http://www.ebi.ac.uk/efo/EFO_0008288 GCST90249595 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorting nexin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 sorting nexin-1 measurement http://www.ebi.ac.uk/efo/EFO_0803092 GCST90249596 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorting nexin-17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 sorting nexin-17 measurement http://www.ebi.ac.uk/efo/EFO_0803093 GCST90249597 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorting nexin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249598 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorting nexin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 sorting nexin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020747 GCST90249599 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sorting nexin-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249600 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lipase member K levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 lipase member K measurement http://www.ebi.ac.uk/efo/EFO_0802711 GCST90248294 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lipase member N levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 lipase member N measurement http://www.ebi.ac.uk/efo/EFO_0801770 GCST90248295 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily A member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248296 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily A member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248297 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily A member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 leukocyte immunoglobulin-like receptor subfamily A member 4 measurement http://www.ebi.ac.uk/efo/EFO_0801765 GCST90248298 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily A member 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 leukocyte immunoglobulin-like receptor subfamily A member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801766 GCST90248299 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily A member 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 leukocyte immunoglobulin-like receptor subfamily A member 6 measurement http://www.ebi.ac.uk/efo/EFO_0801767 GCST90248300 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily B member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90248301 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily B member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90248302 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily B member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 leukocyte immunoglobulin-like receptor subfamily B member 3 measurement http://www.ebi.ac.uk/efo/EFO_0802705 GCST90248303 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily B member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 leukocyte immunoglobulin-like receptor subfamily B member 4 measurement http://www.ebi.ac.uk/efo/EFO_0801768 GCST90248304 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte immunoglobulin-like receptor subfamily B member 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leukocyte immunoglobulin-like receptor subfamily B member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801769 GCST90248305 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lithostathine-1-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 lithostathine-1-alpha measurement http://www.ebi.ac.uk/efo/EFO_0801083 GCST90248306 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lithostathine-1-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248307 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Liver carboxylesterase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248308 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Antibacterial protein LL-37 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248309 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lethal(3)malignant brain tumor-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248310 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leiomodin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leiomodin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802687 GCST90248311 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low molecular weight phosphotyrosine protein phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90248312 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase LNX levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248313 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lon protease homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 lon protease homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801771 GCST90248314 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lactase-phlorizin hydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 lactase-phlorizin hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0801753 GCST90248315 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 leucine-rich repeat-containing protein 15 measurement http://www.ebi.ac.uk/efo/EFO_0801761 GCST90248316 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 24 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248317 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat-containing protein 25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248318 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246802 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0020211 GCST90246803 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246804 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 cadherin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020213 GCST90246805 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cadherin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008060 GCST90246806 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cadherin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020214 GCST90246807 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 cadherin-7 measurement http://www.ebi.ac.uk/efo/EFO_0801438 GCST90246808 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cadherin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246809 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase-related protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246810 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase-related protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 carbonic anhydrase-related protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020233 GCST90246811 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbonic anhydrase-related protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246812 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calbindin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 calbindin measurement http://www.ebi.ac.uk/efo/EFO_0801441 GCST90246813 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcitonin gene-related peptide 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246814 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcineurin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 calcineurin measurement http://www.ebi.ac.uk/efo/EFO_0008061 GCST90246815 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calnexin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calnexin measurement http://www.ebi.ac.uk/efo/EFO_0801444 GCST90246816 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calpain I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calpain I measurement http://www.ebi.ac.uk/efo/EFO_0008064 GCST90246817 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calpastatin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 calpastatin measurement http://www.ebi.ac.uk/efo/EFO_0008065 GCST90246818 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calponin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246819 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calponin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246820 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calsequestrin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246821 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calsyntenin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246822 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calsyntenin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246823 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium/calmodulin-dependent 3,5-cyclic nucleotide phosphodiesterase 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246824 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium/calmodulin-dependent protein kinase type 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 calcium/calmodulin-dependent protein kinase type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008062 GCST90246825 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium/calmodulin-dependent protein kinase type 1D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90246826 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CCAAT/enhancer-binding protein alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246977 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CCAAT/enhancer-binding protein beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 CCAAT/enhancer-binding protein beta measurement http://www.ebi.ac.uk/efo/EFO_0021905 GCST90246978 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenosine deaminase CECR1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246979 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein CEI levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein CEI measurement http://www.ebi.ac.uk/efo/EFO_0801936 GCST90246980 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell adhesion molecule 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0020251 GCST90246981 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell adhesion molecule 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246982 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell adhesion molecule 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cell adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020252 GCST90246983 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Centromere protein V levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246984 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Centromere protein W levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 centromere protein W measurement http://www.ebi.ac.uk/efo/EFO_0802387 GCST90246985 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Centrin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246986 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cerberus levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246987 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ceruloplasmin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246988 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bombesin receptor-activated protein C6orf89 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 bombesin receptor-activated protein C6orf89 measurement http://www.ebi.ac.uk/efo/EFO_0801428 GCST90246989 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246990 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90246991 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90246992 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor H-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 complement factor H-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600054 GCST90246993 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor H-related protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 complement factor H-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0600055 GCST90246994 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor H-related protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 complement factor H-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0600091 GCST90246995 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor H-related protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90246996 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement factor I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 complement factor I measurement http://www.ebi.ac.uk/efo/EFO_0008099 GCST90246997 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chromogranin-A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 chromogranin-A measurement http://www.ebi.ac.uk/efo/EFO_0022021 GCST90246998 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chondroitin sulfate N-acetylgalactosaminyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 chondroitin sulfate N-acetylgalactosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801473 GCST90246999 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Choriogonadotropin subunit beta variant 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 choriogonadotropin subunit beta variant 2 measurement http://www.ebi.ac.uk/efo/EFO_0802396 GCST90247000 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. cGMP-dependent 3,5-cyclic phosphodiesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247001 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cell growth regulator with EF hand domain protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cell growth regulator with EF hand domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801461 GCST90247002 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801483 GCST90247003 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chromodomain-helicase-DNA-binding protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 chromodomain-helicase-DNA-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0802397 GCST90247004 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase CHFR levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247005 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chitinase-3-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 chitinase-3-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801470 GCST90247006 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chitinase-3-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 chitinase-3-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801471 GCST90247007 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acidic mammalian chitinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247008 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase CHIP levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 E3 ubiquitin-protein ligase CHIP measurement http://www.ebi.ac.uk/efo/EFO_0021904 GCST90247009 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chitotriosidase-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247010 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Choline/ethanolamine kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 choline/ethanolamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0021935 GCST90247011 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Charged multivesicular body protein 2a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247012 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Charged multivesicular body protein 2b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247013 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Charged multivesicular body protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 charged multivesicular body protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801469 GCST90247014 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cholinesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247015 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chondroadherin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 chondroadherin measurement http://www.ebi.ac.uk/efo/EFO_0802393 GCST90247016 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chondrocalcin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247017 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcineurin B homologous protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 calcineurin B homologous protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802353 GCST90247018 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcineurin B homologous protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 calcineurin B homologous protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802354 GCST90247019 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chordin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 chordin measurement http://www.ebi.ac.uk/efo/EFO_0802395 GCST90247020 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-regulated heat-stable protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247021 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbohydrate sulfotransferase 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 carbohydrate sulfotransferase 11 measurement http://www.ebi.ac.uk/efo/EFO_0801448 GCST90247022 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbohydrate sulfotransferase 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247023 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbohydrate sulfotransferase 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 carbohydrate sulfotransferase 14 measurement http://www.ebi.ac.uk/efo/EFO_0802366 GCST90247024 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbohydrate sulfotransferase 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90247025 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbohydrate sulfotransferase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247026 Genome-wide genotyping array 2023-05-19 36718908 Pike MM 2023-01-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36718908 Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Childhood median systolic blood pressure percentile 7,393 European ancestry individuals, 2,385 Black individuals NA Illumina [NR] (imputed) 8 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90269916 Genome-wide genotyping array 2023-05-19 36718908 Pike MM 2023-01-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36718908 Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Childhood median systolic blood pressure percentile (0-3 years old) 2,859 Black or European ancestry individuals NA Illumina [NR] (imputed) 11 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90269917 Genome-wide genotyping array 2023-05-19 36718908 Pike MM 2023-01-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36718908 Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Childhood median systolic blood pressure percentile (4-7 years old) 3,142 Black or European ancestry individuals NA Illumina [NR] (imputed) 7 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90269918 Genome-wide genotyping array 2023-05-19 36718908 Pike MM 2023-01-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36718908 Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Childhood median systolic blood pressure percentile (8-12 years old) 4,283 Black or European ancestry individuals NA Illumina [NR] (imputed) 8 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90269919 Genome-wide genotyping array 2023-05-19 36718908 Pike MM 2023-01-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36718908 Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Childhood median systolic blood pressure percentile (13-18 years old) 5,133 Black or European ancestry individuals NA Illumina [NR] (imputed) 10 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90269920 Genome-wide genotyping array 2023-05-19 36718908 Pike MM 2023-01-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36718908 Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Childhood median systolic blood pressure percentile 6,936 European ancestry individuals NA Illumina [NR] (imputed) 7 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90269921 Genome-wide genotyping array 2023-05-19 36718908 Pike MM 2023-01-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36718908 Genetic Variants Associated With Systolic Blood Pressure in Children and Adolescents. Childhood median systolic blood pressure percentile 2,242 Black individuals NA Illumina [NR] (imputed) 14 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90269922 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Migraine (MTAG) 59,674 European ancestry migraine cases, 1,393 European ancestry extracranial cerebral artery dissection cases, 330,494 European ancestry controls NA NR [NR] (imputed) 8 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90103792 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Cervical artery dissection (MTAG) 59,674 European ancestry migraine cases, 1,393 European ancestry extracranial cerebral artery dissection cases, 330,494 European ancestry controls NA NR [NR] (imputed) 8 cervical artery dissection http://www.ebi.ac.uk/efo/EFO_1000059 GCST90103794 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Migraine (MTAG) 5,386 European ancestry small vessel stroke cases, 59,674 European ancestry migraine cases, 659,638 European ancestry controls NA NR [NR] (imputed) 1 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90269766 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Small vessel stroke (MTAG) 5,386 European ancestry small vessel stroke cases, 59,674 European ancestry migraine cases, 659,638 European ancestry controls NA NR [NR] (imputed) 1 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90103795 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Migraine without aura (MTAG) 8,348 European ancestry migraine without aura cases, 1,393 European ancestry extracranial cerebral artery dissection cases, 154,038 European ancestry controls NA NR [NR] (imputed) 3 migraine without aura http://purl.obolibrary.org/obo/MONDO_0100431 GCST90103793 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Cervical artery dissection (MTAG) 8,348 European ancestry migraine without aura cases, 1,393 European ancestry extracranial cerebral artery dissection cases, 154,038 European ancestry controls NA NR [NR] (imputed) 3 cervical artery dissection http://www.ebi.ac.uk/efo/EFO_1000059 GCST90269767 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Large artery stroke (MTAG) 4,373 European ancestry large vessel stroke cases, 59,674 European ancestry migraine cases, 613,368 European ancestry controls NA NR [NR] (imputed) 1 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90103796 Genome-wide genotyping array 2023-05-10 35128049 Daghals I 2022-02-01 Neurol Genet www.ncbi.nlm.nih.gov/pubmed/35128049 Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement. Migraine (MTAG) 4,373 European ancestry large vessel stroke cases, 59,674 European ancestry migraine cases, 613,368 European ancestry controls NA NR [NR] (imputed) 1 migraine disorder http://purl.obolibrary.org/obo/MONDO_0005277 GCST90269768 Genome-wide genotyping array 2023-11-24 37945903 Wang A 2023-11-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37945903 Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Prostate cancer 122,188 European ancestry cases, 604,640 European ancestry controls NA Affymetrix, Illumina [27244980] (imputed) 406 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90274714 Genome-wide genotyping array 2023-11-24 37945903 Wang A 2023-11-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37945903 Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Prostate cancer 19,391 African American or Afro-Caribbean cases, 61,608 African American or Afro-Caribbean controls NA Affymetrix, Illumina [27753840] (imputed) 66 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90274715 Genome-wide genotyping array 2023-11-24 37945903 Wang A 2023-11-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37945903 Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Prostate cancer 10,809 East Asian ancestry cases, 95,790 East Asian ancestry controls NA Affymetrix, Illumina [11465277] (imputed) 62 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90274716 Genome-wide genotyping array 2023-11-24 37945903 Wang A 2023-11-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37945903 Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Prostate cancer 3,931 Hispanic or Latin American cases, 26,405 Hispanic or Latin American controls NA Affymetrix, Illumina [26567548] (imputed) 19 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90274717 Genome-wide genotyping array 2023-11-24 37945903 Wang A 2023-11-09 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37945903 Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants. Prostate cancer 122,188 European ancestry cases, 604,640 European ancestry controls, 19,391 African American or Afro-Caribbean cases, 61,608 African American or Afro-Caribbean controls, 10,809 East Asian ancestry cases, 95,790 East Asian ancestry controls, 3,931 Hispanic or Latin American cases, 26,405 Hispanic or Latin American controls NA Affymetrix, Illumina [42428922] (imputed) 449 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90274713 Genome-wide genotyping array 2023-06-05 35971929 Lin L 2022-08-16 Endokrynol Pol www.ncbi.nlm.nih.gov/pubmed/35971929 Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people. Fasting proinsulin levels in prediabetes 451 Han Chinese ancestry individuals NA NR [NR] (imputed) 3 proinsulin measurement http://www.ebi.ac.uk/efo/EFO_0010814 GCST90270123 Genome-wide genotyping array 2023-06-05 35971929 Lin L 2022-08-16 Endokrynol Pol www.ncbi.nlm.nih.gov/pubmed/35971929 Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people. Fasting insulin levels in prediabetes 451 Han Chinese ancestry individuals NA NR [NR] (imputed) 1 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST90270124 Genome-wide genotyping array 2023-06-05 35971929 Lin L 2022-08-16 Endokrynol Pol www.ncbi.nlm.nih.gov/pubmed/35971929 Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people. 2-hour postprandial proinsulin levels in prediabetes 451 Han Chinese ancestry individuals NA NR [NR] (imputed) 2 proinsulin measurement http://www.ebi.ac.uk/efo/EFO_0010814 GCST90270125 Genome-wide genotyping array 2023-06-05 35971929 Lin L 2022-08-16 Endokrynol Pol www.ncbi.nlm.nih.gov/pubmed/35971929 Genome-wide association study of fasting proinsulin, fasting insulin, 2-hour postprandial proinsulin, and 2-hour postprandial insulin in Chinese Han people. 2-hour postprandial insulin levels in prediabetes 451 Han Chinese ancestry individuals NA NR [NR] (imputed) 3 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90270126 Genome-wide genotyping array 2023-03-01 36672800 Orlova E 2022-12-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672800 Association of Early Childhood Caries with Bitter Taste Receptors: A Meta-Analysis of Genome-Wide Association Studies and Transcriptome-Wide Association Study. Early childhood caries 2,974 European ancestry individuals NA NR [3988879] (imputed) 7 primary dental caries http://www.ebi.ac.uk/efo/EFO_0600095 GCST90255389 Genome-wide genotyping array 2023-11-08 35172313 Alotaibi RN 2022-02-16 Hum Hered www.ncbi.nlm.nih.gov/pubmed/35172313 Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts. Enamel hypoplasia 7,159 European and unknown ancestry individuals NA Illumina [5375488] (imputed) 10 Dental enamel hypoplasia http://www.ebi.ac.uk/efo/EFO_1001304 GCST90103973 Genome-wide genotyping array 2023-03-01 32587327 Tsepilov YA 2020-06-25 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32587327 Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. Genetically independent pain phenotypes (GIP2) 265,000 European ancestry individuals 174,831 European ancestry individuals, 7,541 African ancestry individuals, 9,208 South Asian ancestry individuals Affymetrix [NR] (imputed) 3 chronic musculoskeletal pain http://www.ebi.ac.uk/efo/EFO_0022195 GCST90245880 Genome-wide genotyping array 2023-03-01 32587327 Tsepilov YA 2020-06-25 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32587327 Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. Genetically independent pain phenotypes (GIP3) 265,000 European ancestry individuals 174,831 European ancestry individuals, 7,541 African ancestry individuals, 9,208 South Asian ancestry individuals Affymetrix [NR] (imputed) 0 chronic musculoskeletal pain http://www.ebi.ac.uk/efo/EFO_0022195 GCST90245881 Genome-wide genotyping array 2023-03-01 32587327 Tsepilov YA 2020-06-25 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32587327 Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. Genetically independent pain phenotypes (GIP4) 265,000 European ancestry individuals 174,831 European ancestry individuals, 7,541 African ancestry individuals, 9,208 South Asian ancestry individuals Affymetrix [NR] (imputed) 0 chronic musculoskeletal pain http://www.ebi.ac.uk/efo/EFO_0022195 GCST90245882 Genome-wide genotyping array 2023-03-01 32587327 Tsepilov YA 2020-06-25 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32587327 Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. Neck pain or shoulder pain 439,831 European ancestry individuals NA Affymetrix [NR] (imputed) 1 Neck pain http://purl.obolibrary.org/obo/HP_0030833 GCST90245883 Genome-wide genotyping array 2023-03-01 32587327 Tsepilov YA 2020-06-25 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32587327 Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. Hip pain 439,831 European ancestry individuals NA Affymetrix [NR] (imputed) 1 Hip pain http://purl.obolibrary.org/obo/HP_0030838 GCST90245884 Genome-wide genotyping array 2023-03-01 32587327 Tsepilov YA 2020-06-25 Commun Biol www.ncbi.nlm.nih.gov/pubmed/32587327 Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions. Genetically independent pain phenotypes (GIP1) 265,000 European ancestry individuals 174,831 European ancestry individuals, 7,541 African ancestry individuals, 9,208 South Asian ancestry individuals Affymetrix [NR] (imputed) 6 chronic musculoskeletal pain http://www.ebi.ac.uk/efo/EFO_0022195 GCST90245879 Genome-wide genotyping array 2023-03-10 36778051 Tsuo K 2022-11-08 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36778051 Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity. Asthma 5,051 African ancestry cases, 27,607 African ancestry controls, 4,069 Hispanic or Latin American cases, 14,104 Hispanic or Latin American controls, 4,015 Central Asian ancestry cases, 27,091 Central Asian ancestry controls, 4,015 South Asian ancestry cases, 27,091 South Asian ancestry controls, 18,549 East Asian ancestry cases, 322,655 East Asian ancestry controls, 121,940 European ancestry cases, 1,254,131 European ancestry controls, 139 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 1,434 Greater Middle Eastern (Middle Eastern, North African or Persian) controls 2,455 African ancestry cases, 7,542 African ancestry controls, 180 Hispanic or Latin American cases, 1,325 Hispanic or Latin American controls, 5,981 European ancestry cases, 42,054 European ancestry controls, 1,375 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 12,684 Greater Middle Eastern (Middle Eastern, North African or Persian) controls NR [70800000] 4 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90255667 Genome-wide genotyping array 2023-03-10 36778051 Tsuo K 2022-11-08 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36778051 Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity. Age of onset of adult onset asthma 56,744 European ancestry cases, 674,014 European ancestry controls NA NR [NR] 70 age of onset of asthma http://purl.obolibrary.org/obo/OBA_2001001 GCST90255668 Genome-wide genotyping array 2023-03-10 36778051 Tsuo K 2022-11-08 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36778051 Multi-ancestry meta-analysis of asthma identifies novel associations and highlights the value of increased power and diversity. Age of onset of childhood onset asthma 20,964 European ancestry cases, 674,014 European ancestry controls NA NR [NR] 90 age of onset of childhood onset asthma http://purl.obolibrary.org/obo/OBA_2001015 GCST90255669 Genome-wide genotyping array 2023-03-01 36656851 Hui D 2023-01-19 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36656851 Gene burden analysis identifies genes associated with increased risk and severity of adult-onset hearing loss in a diverse hospital-based cohort. Hearing loss 859 European ancestry cases, 26,292 European ancestry controls, 251 African American or Afro-Caribbean cases, 9,105 African American or Afro-Caribbean controls NA Illumina [11977860] (imputed) 1 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90244103 Genome-wide genotyping array 2023-11-23 37245863 Vasavda C 2023-05-26 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37245863 A polygenic risk score for predicting racial and genetic susceptibility to prurigo nodularis. Prurigo nodularis 309 Finnish ancestry cases, 198,740 Finnish ancestry controls NA Affymetrix, Illumina [16380425] (imputed) 2 prurigo nodularis http://purl.obolibrary.org/obo/MONDO_0026045 GCST90297844 Genome-wide genotyping array 2023-11-23 37245863 Vasavda C 2023-05-26 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37245863 A polygenic risk score for predicting racial and genetic susceptibility to prurigo nodularis. Prurigo nodularis 171 European ancestry cases, 36,328 European ancestry controls NA Illumina [6874147] (imputed) 1 prurigo nodularis http://purl.obolibrary.org/obo/MONDO_0026045 GCST90297845 Genome-wide genotyping array 2023-11-23 37245863 Vasavda C 2023-05-26 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37245863 A polygenic risk score for predicting racial and genetic susceptibility to prurigo nodularis. Prurigo nodularis 480 European ancestry cases, 235,068 European ancestry controls NA Affymetrix, Illumina [6572020] (imputed) 0 prurigo nodularis http://purl.obolibrary.org/obo/MONDO_0026045 GCST90297846 Genome-wide genotyping array 2023-02-27 36662838 Slomian D 2023-01-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/36662838 Better safe than sorry-Whole-genome sequencing indicates that missense variants are significant in susceptibility to COVID-19. Severe COVID-19 infection 235 severe cases, up to 841 resistant, benign or mild controls NA Illumina [15489173] 603 severe acute respiratory syndrome, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000694, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255357 Genome-wide sequencing 2023-02-27 36662838 Slomian D 2023-01-20 PLoS One www.ncbi.nlm.nih.gov/pubmed/36662838 Better safe than sorry-Whole-genome sequencing indicates that missense variants are significant in susceptibility to COVID-19. Resistance to COVID-19 infection (Exposed negative vs positive) 306 resistant cases, up to 770 benign, mild or severe controls NA Illumina [15489173] 522 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255358 Genome-wide sequencing 2023-03-21 36672180 Tirozzi A 2023-01-06 Cells www.ncbi.nlm.nih.gov/pubmed/36672180 A Multi-Trait Association Analysis of Brain Disorders and Platelet Traits Identifies Novel Susceptibility Loci for Major Depression, Alzheimer's and Parkinson's Disease. Alzheimer disease (MTAG) at least 71,880 European ancestry cases, at least 383,378 European ancestry controls NA NR [4540326] 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90256603 Genome-wide genotyping array 2023-03-21 36672180 Tirozzi A 2023-01-06 Cells www.ncbi.nlm.nih.gov/pubmed/36672180 A Multi-Trait Association Analysis of Brain Disorders and Platelet Traits Identifies Novel Susceptibility Loci for Major Depression, Alzheimer's and Parkinson's Disease. Parkinson disease (MTAG) at least 37,688 European ancestry cases, at least 18,618 European ancestry controls NA NR [4540326] 2 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90256604 Genome-wide genotyping array 2023-04-14 36576985 Carreras-Torres R 2022-12-28 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/36576985 Genome-wide interaction study with smoking for colorectal cancer risk identifies novel genetic loci related to tumor suppression, inflammation and immune response. Colorectal cancer x smoking status interaction (1df) 18,781 European ancestry ever-smoker cases, 14,975 European ancestry never-smoker cases, 22,370 European ancestry ever-smoker controls, 21,976 European ancestry never-smoker controls NA Affymetrix, Illumina [7200000] (imputed) 0 smoking status measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0006527, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90267392 Genome-wide genotyping array 2023-04-14 36576985 Carreras-Torres R 2022-12-28 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/36576985 Genome-wide interaction study with smoking for colorectal cancer risk identifies novel genetic loci related to tumor suppression, inflammation and immune response. Colorectal cancer x smoking status interaction (3df) 18,781 European ancestry ever-smoker cases, 14,975 European ancestry never-smoker cases, 22,370 European ancestry ever-smoker controls, 21,976 European ancestry never-smoker controls NA Affymetrix, Illumina [7200000] (imputed) 1 smoking status measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0006527, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90267393 Genome-wide genotyping array 2023-04-14 36576985 Carreras-Torres R 2022-12-28 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/36576985 Genome-wide interaction study with smoking for colorectal cancer risk identifies novel genetic loci related to tumor suppression, inflammation and immune response. Colorectal cancer x cigarettes per day interaction (1df) 13,320 European ancestry cases, 16,176 European ancestry controls NA Affymetrix, Illumina [7200000] (imputed) 2 colorectal cancer, cigarettes per day measurement http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0006525 GCST90267394 Genome-wide genotyping array 2023-04-14 36576985 Carreras-Torres R 2022-12-28 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/36576985 Genome-wide interaction study with smoking for colorectal cancer risk identifies novel genetic loci related to tumor suppression, inflammation and immune response. Colorectal cancer x cigarettes per day interaction (3df) 13,320 European ancestry cases, 16,176 European ancestry controls NA Affymetrix, Illumina [7200000] (imputed) 2 colorectal cancer, cigarettes per day measurement http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0006525 GCST90267395 Genome-wide genotyping array 2023-04-14 36576985 Carreras-Torres R 2022-12-28 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/36576985 Genome-wide interaction study with smoking for colorectal cancer risk identifies novel genetic loci related to tumor suppression, inflammation and immune response. Colorectal cancer x pack-years of smoking interaction (1df) 12,531 European ancestry cases, 15,271 European ancestry controls NA Affymetrix, Illumina [7200000] (imputed) 0 pack-years measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0006526, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90267396 Genome-wide genotyping array 2023-04-14 36576985 Carreras-Torres R 2022-12-28 Cancer Epidemiol Biomarkers Prev www.ncbi.nlm.nih.gov/pubmed/36576985 Genome-wide interaction study with smoking for colorectal cancer risk identifies novel genetic loci related to tumor suppression, inflammation and immune response. Colorectal cancer x pack-years of smoking interaction (3df) 12,531 European ancestry cases, 15,271 European ancestry controls NA Affymetrix, Illumina [7200000] (imputed) 0 pack-years measurement, colorectal cancer http://www.ebi.ac.uk/efo/EFO_0006526, http://purl.obolibrary.org/obo/MONDO_0005575 GCST90267397 Genome-wide genotyping array 2023-06-27 36828809 Han Y 2023-02-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36828809 Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis. Primary sclerosing cholangitis (MTAG) at least 2,871 European ancestry cases, at least 12,019 European ancestry controls (MTAG boosted by autoimmune-related disease samples) at least 952 cases, 231,644 controls (MTAG boosted by autoimmune-related disease samples) NR [8412578] (imputed) 21 sclerosing cholangitis http://www.ebi.ac.uk/efo/EFO_0004268 GCST90271580 Genome-wide genotyping array 2023-05-30 36817429 Cardinale CJ 2023-02-01 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36817429 Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulator. Type 1 diabetes (age at diagnosis) 4,014 European ancestry cases 493 European ancestry cases Illumina [6988016] (imputed) 1 age of onset of type 1 diabetes mellitus http://purl.obolibrary.org/obo/OBA_2001012 GCST90270077 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Translationally-controlled tumor protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 translationally-controlled tumor protein measurement http://www.ebi.ac.uk/efo/EFO_0020784 GCST90249791 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor type 1-associated DEATH domain protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249792 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Teratocarcinoma-derived growth factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90249793 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tectonic-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249794 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription elongation factor A protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249795 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription elongation factor A protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249796 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM3B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90247536 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protease serine 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249925 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein PVRIG levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane protein PVRIG measurement http://www.ebi.ac.uk/efo/EFO_0803192 GCST90249926 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane and ubiquitin-like domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane and ubiquitin-like domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803175 GCST90249927 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin-related transmembrane protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249928 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein disulfide-isomerase TMX3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249929 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90249930 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tenomodulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tenomodulin measurement http://www.ebi.ac.uk/efo/EFO_0803142 GCST90249931 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Troponin I, fast skeletal muscle levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 troponin i, fast skeletal muscle measurement http://www.ebi.ac.uk/efo/EFO_0020789 GCST90249932 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Troponin I, cardiac muscle levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 troponin i, cardiac muscle measurement http://www.ebi.ac.uk/efo/EFO_0020788 GCST90249933 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Troponin T, fast skeletal muscle levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249934 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trinucleotide repeat-containing gene 6B protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249935 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TOM1-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 TOM1-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802136 GCST90249936 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TOM1-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249937 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TOMM20-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249938 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Torsin-1A-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 torsin-1A-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802137 GCST90249939 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Torsin-4A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249940 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TOX high mobility group box family member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 TOX high mobility group box family member 3 measurement http://www.ebi.ac.uk/efo/EFO_0803161 GCST90249941 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thymidine phosphorylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249942 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tryptophan 2,3-dioxygenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249943 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TP53-regulated inhibitor of apoptosis 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249944 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tissue-type plasminogen activator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tissue-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0020776 GCST90249945 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thiopurine S-methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249946 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombopoietin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 thrombopoietin measurement http://www.ebi.ac.uk/efo/EFO_0022004 GCST90249947 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombopoietin Receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thrombopoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020769 GCST90249948 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tripeptidyl-peptidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249949 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trafficking protein particle complex subunit 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249950 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trafficking protein particle complex subunit 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249951 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trafficking protein particle complex subunit 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249952 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tubulin polymerization-promoting protein family member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tubulin polymerization-promoting protein family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0802164 GCST90249953 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EKC/KEOPS complex subunit TPRKB levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249954 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tryptase beta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90249955 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tapasin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tapasin measurement http://www.ebi.ac.uk/efo/EFO_0802118 GCST90249956 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tapasin-related protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tapasin-related protein measurement http://www.ebi.ac.uk/efo/EFO_0802119 GCST90249957 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tryptophan--tRNA ligase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249958 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transaldolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249959 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TNF receptor-associated factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249960 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TNF receptor-associated factor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 TNF receptor-associated factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0803158 GCST90249961 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TRAF family member-associated NF-kappa-B activator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249962 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell receptor-associated transmembrane adapter 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 t-cell receptor-associated transmembrane adapter 1 measurement http://www.ebi.ac.uk/efo/EFO_0803131 GCST90249963 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tartrate-resistant acid phosphatase type 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90249964 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription regulator protein BACH1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 transcription regulator protein BACH1 measurement http://www.ebi.ac.uk/efo/EFO_0802141 GCST90249965 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription regulator protein BACH2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 transcription regulator protein BACH2 measurement http://www.ebi.ac.uk/efo/EFO_0803164 GCST90249966 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcobalamin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249967 Genome-wide genotyping array 2023-04-25 36629403 Khor CC 2023-01-11 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36629403 Cross-ancestry GWAS defines the extended CYP2D6 locus as the principal genetic determinant of endoxifen plasma concentrations. Endoxifen levels in tamoxifen-treated hormone-receptor-positive breast cancer 148 Singaporean Chinese ancestry individuals, 69 Lebanese ancestry individuals, 280 German ancestry individuals NA Illumina [4673513] (imputed) 5 response to tamoxifen http://www.ebi.ac.uk/efo/EFO_0009391 GCST90267629 Genome-wide genotyping array 2023-04-25 36629403 Khor CC 2023-01-11 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36629403 Cross-ancestry GWAS defines the extended CYP2D6 locus as the principal genetic determinant of endoxifen plasma concentrations. (Z)-4-hydroxytamoxifen levels in tamoxifen-treated hormone-receptor-positive breast cancer 148 Singaporean Chinese ancestry individuals, 69 Lebanese ancestry individuals, 280 German ancestry individuals NA Illumina [4673513] (imputed) 2 response to tamoxifen http://www.ebi.ac.uk/efo/EFO_0009391 GCST90267630 Genome-wide genotyping array 2023-04-25 36629403 Khor CC 2023-01-11 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36629403 Cross-ancestry GWAS defines the extended CYP2D6 locus as the principal genetic determinant of endoxifen plasma concentrations. N-desmethyl tamoxifen levels in tamoxifen-treated hormone-receptor-positive breast cancer 148 Singaporean Chinese ancestry individuals, 69 Lebanese ancestry individuals, 280 German ancestry individuals NA Illumina [4673513] (imputed) 5 response to tamoxifen http://www.ebi.ac.uk/efo/EFO_0009391 GCST90267631 Genome-wide genotyping array 2023-04-25 36629403 Khor CC 2023-01-11 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36629403 Cross-ancestry GWAS defines the extended CYP2D6 locus as the principal genetic determinant of endoxifen plasma concentrations. Tamoxifen levels in tamoxifen-treated hormone-receptor-positive breast cancer 148 Singaporean Chinese ancestry individuals, 69 Lebanese ancestry individuals, 280 German ancestry individuals NA Illumina [4673513] (imputed) 0 response to tamoxifen http://www.ebi.ac.uk/efo/EFO_0009391 GCST90267632 Genome-wide genotyping array 2023-04-25 36629403 Khor CC 2023-01-11 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36629403 Cross-ancestry GWAS defines the extended CYP2D6 locus as the principal genetic determinant of endoxifen plasma concentrations. (Z)-4-hydroxytamoxifen to tamoxifen ratio in tamoxifen-treated hormone-receptor-positive breast cancer 148 Singaporean Chinese ancestry individuals, 69 Lebanese ancestry individuals, 280 German ancestry individuals NA Illumina [4673513] (imputed) 6 response to tamoxifen http://www.ebi.ac.uk/efo/EFO_0009391 GCST90267634 Genome-wide genotyping array 2023-04-25 36629403 Khor CC 2023-01-11 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36629403 Cross-ancestry GWAS defines the extended CYP2D6 locus as the principal genetic determinant of endoxifen plasma concentrations. Endoxifen to N-desmethyl tamoxifen ratio in tamoxifen-treated hormone-receptor-positive breast cancer 148 Singaporean Chinese ancestry individuals, 69 Lebanese ancestry individuals, 280 German ancestry individuals NA Illumina [4673513] (imputed) 4 response to tamoxifen http://www.ebi.ac.uk/efo/EFO_0009391 GCST90267633 Genome-wide genotyping array 2023-08-08 37492417 Bhattacharjee E 2023-04-18 Lancet Reg Health Southeast Asia www.ncbi.nlm.nih.gov/pubmed/37492417 Genetic variants associated with spontaneous preterm birth in women from India: a prospective cohort study. Spontaneous preterm birth (maternal effect) 521 Indian ancestry preterm birth mothers, 1,042 Indian ancestry term birth mothers NA Illumina [233748] (imputed) 3 spontaneous preterm birth, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0006917, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90179179 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor necrosis factor receptor superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020807 GCST90249836 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 19 measurement http://www.ebi.ac.uk/efo/EFO_0020808 GCST90249837 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 19L levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90249838 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor necrosis factor receptor superfamily member 1A measurement http://www.ebi.ac.uk/efo/EFO_0803201 GCST90249839 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90249840 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 21 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tumor necrosis factor receptor superfamily member 21 measurement http://www.ebi.ac.uk/efo/EFO_0020810 GCST90249841 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 27 measurement http://www.ebi.ac.uk/efo/EFO_0020812 GCST90249842 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tumor necrosis factor receptor superfamily member 3 measurement http://www.ebi.ac.uk/efo/EFO_0020813 GCST90249843 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020814 GCST90249844 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90249845 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 6B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 6B measurement http://www.ebi.ac.uk/efo/EFO_0020815 GCST90249846 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor necrosis factor receptor superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0020816 GCST90249847 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90249848 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor receptor superfamily member EDAR levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 tumor necrosis factor receptor superfamily member EDAR measurement http://www.ebi.ac.uk/efo/EFO_0008310 GCST90249849 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription factor SOX-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249850 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcription factor TFIIIB component B homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249851 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transforming growth factor beta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transforming growth factor beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020781 GCST90249852 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transforming growth factor beta-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transforming growth factor beta-3 measurement http://www.ebi.ac.uk/efo/EFO_0020782 GCST90249853 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transforming growth factor-beta-induced protein ig-h3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 transforming growth factor-beta-induced protein ig-h3 measurement http://www.ebi.ac.uk/efo/EFO_0008302 GCST90249854 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transforming growth factor beta receptor type 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 transforming growth factor beta receptor type 3 measurement http://www.ebi.ac.uk/efo/EFO_0020779 GCST90249855 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane glycoprotein NMB levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90249856 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thromboxane-A synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 thromboxane-A synthase measurement http://www.ebi.ac.uk/efo/EFO_0803152 GCST90249857 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable tRNA(His) guanylyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249858 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acetyl-CoA acetyltransferase, cytosolic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249859 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-ketoacyl-CoA thiolase, peroxisomal levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249860 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acetyl-CoA acetyltransferase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249861 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. THO complex subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249862 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 thrombin measurement http://www.ebi.ac.uk/efo/EFO_0020768 GCST90249863 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249864 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombospondin type-1 domain-containing protein 7A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thrombospondin type-1 domain-containing protein 7A measurement http://www.ebi.ac.uk/efo/EFO_0803150 GCST90249865 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombospondin type-1 domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 thrombospondin type-1 domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802131 GCST90249866 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thiosulfate sulfurtransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 thiosulfate sulfurtransferase measurement http://www.ebi.ac.uk/efo/EFO_0802130 GCST90249867 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thymocyte nuclear protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 thymocyte nuclear protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802132 GCST90249868 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thyroglobulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 thyroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010050 GCST90249869 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-lymphoma invasion and metastasis-inducing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249870 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trimeric intracellular cation channel type B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249871 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Testican-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 testican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020766 GCST90249872 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Testican-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 testican-3 measurement http://www.ebi.ac.uk/efo/EFO_0802124 GCST90249873 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Translation initiation factor IF-3, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249874 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell immunoreceptor with Ig and ITIM domains levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249875 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Type II inositol 1,4,5-trisphosphate 5-phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249876 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitochondrial import inner membrane translocase subunit TIM14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 mitochondrial import inner membrane translocase subunit tim14 measurement http://www.ebi.ac.uk/efo/EFO_0020573 GCST90249877 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitochondrial import inner membrane translocase subunit Tim21 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249878 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-cell immunoglobulin and mucin domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249879 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tubulointerstitial nephritis antigen-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tubulointerstitial nephritis antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0803197 GCST90249880 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Toll-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 toll-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0802133 GCST90249881 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Toll/interleukin-1 receptor domain-containing adapter protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 toll/interleukin-1 receptor domain-containing adapter protein measurement http://www.ebi.ac.uk/efo/EFO_0802134 GCST90249882 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TIR domain-containing adapter molecule 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249883 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Titin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 titin measurement http://www.ebi.ac.uk/efo/EFO_0803157 GCST90249884 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thymidylate kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249885 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Impulsive action factor 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270100 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Impulsive choice factor 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270101 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Impulsive personality factor 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270102 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Impulsive action (No-Go trial accuracy) 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270103 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Impulsive action (Go trial accuracy) 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270104 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Delayed reward discounting 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 delayed reward discounting measurement http://www.ebi.ac.uk/efo/EFO_0008476 GCST90270105 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Delayed reward discounting (small magnitude rewards) 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 delayed reward discounting measurement http://www.ebi.ac.uk/efo/EFO_0008476 GCST90270106 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Delayed reward discounting (medium magnitude rewards) 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 delayed reward discounting measurement http://www.ebi.ac.uk/efo/EFO_0008476 GCST90270107 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Delayed reward discounting (large magnitude rewards) 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 delayed reward discounting measurement http://www.ebi.ac.uk/efo/EFO_0008476 GCST90270108 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Negative urgency 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270109 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Lack of perseverance 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270110 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Lack of premeditation 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270111 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Positive urgency 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270112 Genome-wide genotyping array 2023-06-06 37060189 Deng WQ 2023-04-14 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37060189 Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults. Sensation seeking 1,534 European ancestry individuals NA Illumina [5748667] (imputed) 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90270113 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Very long-chain specific acyl-CoA dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250179 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Very long-chain acyl-CoA synthetase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 very long-chain acyl-CoA synthetase measurement http://www.ebi.ac.uk/efo/EFO_0802211 GCST90250180 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Very low-density lipoprotein receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250181 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular non-inflammatory molecule 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250182 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vacuolar protein sorting-associated protein 26A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250183 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicular, overexpressed in cancer, prosurvival protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250184 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. VPS10 domain-containing receptor SorCS1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250185 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vacuolar protein sorting-associated protein 28 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250186 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vacuolar protein sorting-associated protein 29 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 vacuolar protein sorting-associated protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0802207 GCST90250187 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vacuolar protein sorting-associated protein 4B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vacuolar protein sorting-associated protein 4B measurement http://www.ebi.ac.uk/efo/EFO_0802209 GCST90250188 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vacuolar protein sorting-associated protein VTA1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vacuolar protein sorting-associated protein VTA1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020845 GCST90250189 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. V(D)J recombination-activating protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250190 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle-trafficking protein SEC22a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vesicle-trafficking protein SEC22a measurement http://www.ebi.ac.uk/efo/EFO_0803256 GCST90250191 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. V-set and immunoglobulin domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 v-set and immunoglobulin domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803245 GCST90250192 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. V-set and immunoglobulin domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 v-set and immunoglobulin domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803308 GCST90250193 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. V-set and transmembrane domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 v-set and transmembrane domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803247 GCST90250194 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle transport through interaction with t-SNAREs homolog 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vesicle transport through interaction with t-SNAREs homolog 1A measurement http://www.ebi.ac.uk/efo/EFO_0803250 GCST90250195 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle transport through interaction with t-SNAREs homolog 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vesicle transport through interaction with t-SNAREs homolog 1B measurement http://www.ebi.ac.uk/efo/EFO_0802212 GCST90250196 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicular integral-membrane protein VIP36 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 vesicular integral-membrane protein VIP36 measurement http://www.ebi.ac.uk/efo/EFO_0022012 GCST90250197 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. von Willebrand factor A domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250198 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. von Willebrand factor A domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250199 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. von Willebrand factor C domain-containing protein 2-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 von Willebrand factor C domain-containing protein 2-like measurement http://www.ebi.ac.uk/efo/EFO_0803259 GCST90250200 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. von Willebrand factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90250201 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP four-disulfide core domain protein 10A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 WAP four-disulfide core domain protein 10A measurement http://www.ebi.ac.uk/efo/EFO_0803260 GCST90250202 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein WFDC10B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250203 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein ABHD14A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246405 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Abelson tyrosine-protein kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 Abelson tyrosine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008012 GCST90246406 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Actin-binding LIM protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 actin-binding LIM protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802251 GCST90246407 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amiloride-sensitive amine oxidase [copper-containing] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246408 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arachidonate 15-lipoxygenase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 arachidonate 15-lipoxygenase B measurement http://www.ebi.ac.uk/efo/EFO_0801391 GCST90246409 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acyl-CoA-binding domain-containing protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 acyl-CoA-binding domain-containing protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801342 GCST90246410 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acyl-CoA-binding domain-containing protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 acyl-CoA-binding domain-containing protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0801343 GCST90246411 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acyl-CoA-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246412 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiotensin-converting enzyme levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 angiotensin-converting enzyme measurement http://www.ebi.ac.uk/efo/EFO_0006515 GCST90246413 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Angiotensin-converting enzyme 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 angiotensin-converting enzyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0020150 GCST90246414 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acetylcholinesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246415 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acid ceramidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 acid ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0801339 GCST90246416 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent Clp protease proteolytic subunit, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246417 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acyl-coenzyme A thioesterase 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246418 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acyl-coenzyme A thioesterase 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246419 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 2-phosphoxylose phosphatase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 2-phosphoxylose phosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803305 GCST90246420 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Activin receptor type-2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246421 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-actinin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246422 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-actinin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246423 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aspartoacylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246424 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acylphosphatase-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 acylphosphatase-2 measurement http://www.ebi.ac.uk/efo/EFO_0801344 GCST90246425 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A disintegrin and metalloproteinase with thrombospondin motifs 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 1 measurement http://www.ebi.ac.uk/efo/EFO_0021968 GCST90246426 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A disintegrin and metalloproteinase with thrombospondin motifs 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90246427 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A disintegrin and metalloproteinase with thrombospondin motifs 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 15 measurement http://www.ebi.ac.uk/efo/EFO_0020123 GCST90246428 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A disintegrin and metalloproteinase with thrombospondin motifs 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 a disintegrin and metalloproteinase with thrombospondin motifs 3 measurement http://www.ebi.ac.uk/efo/EFO_0802245 GCST90246429 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A disintegrin and metalloproteinase with thrombospondin motifs 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 4 measurement http://www.ebi.ac.uk/efo/EFO_0020124 GCST90246430 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A disintegrin and metalloproteinase with thrombospondin motifs 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90246431 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. A disintegrin and metalloproteinase with thrombospondin motifs 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 6 measurement http://www.ebi.ac.uk/efo/EFO_0801338 GCST90246432 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alcohol dehydrogenase 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246433 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alcohol dehydrogenase 1C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246434 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alcohol dehydrogenase class-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246435 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alcohol dehydrogenase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 alcohol dehydrogenase 4 measurement http://www.ebi.ac.uk/efo/EFO_0802261 GCST90246436 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alcohol dehydrogenase class 4 mu/sigma chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246437 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alcohol dehydrogenase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246438 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adiponectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90246439 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenosine kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246440 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADM2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246441 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. [Protein ADP-ribosylarginine] hydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246442 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ADP-sugar pyrophosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246443 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adrenomedullin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 adrenomedullin measurement http://www.ebi.ac.uk/efo/EFO_0010909 GCST90246444 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proteasomal ubiquitin receptor ADRM1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246445 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adseverin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 adseverin measurement http://www.ebi.ac.uk/efo/EFO_0801358 GCST90246446 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-endosulfine levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246447 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Amino-terminal enhancer of split levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246448 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Actin filament-associated protein 1-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246449 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Afamin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 afamin measurement http://www.ebi.ac.uk/efo/EFO_0008015 GCST90246450 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. alpha-Fetoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246451 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-galactosidase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246452 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246453 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246454 Genome-wide genotyping array 2023-07-18 37429843 Rasooly D 2023-07-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37429843 Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure. Heart failure 90,653 European ancestry cases, 1,188,957 European ancestry controls NA Affymetrix [10227138] (imputed) 39 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90274223 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. FAD-dependent oxidoreductase domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247650 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fragile X mental retardation syndrome-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fragile X mental retardation syndrome-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802555 GCST90247651 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. G0/G1 switch protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 G0/G1 switch protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802559 GCST90247652 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. G2/mitotic-specific cyclin-B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247653 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Galactose-3-O-sulfotransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247654 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycerol-3-phosphate dehydrogenase 1-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 glycerol-3-phosphate dehydrogenase 1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801640 GCST90247655 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glycerol-3-phosphate phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247656 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glucosamine 6-phosphate N-acetyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 glucosamine 6-phosphate N-acetyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0801626 GCST90247657 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-aminobutyric acid receptor-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247658 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-aminobutyric acid receptor-associated protein-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 gamma-aminobutyric acid receptor-associated protein-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0801613 GCST90247659 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-aminobutyric acid receptor-associated protein-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 gamma-aminobutyric acid receptor-associated protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801614 GCST90247660 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-aminobutyric acid type B receptor subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247661 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Gamma-aminobutyric acid type B receptor subunit 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 gamma-aminobutyric acid type B receptor subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0801615 GCST90247662 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Growth arrest and DNA damage-inducible proteins-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 growth arrest and DNA damage-inducible proteins-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803291 GCST90247663 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein argonaute-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248846 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plasminogen activator inhibitor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90248847 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pancreatic hormone levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pancreatic hormone measurement http://www.ebi.ac.uk/efo/EFO_0020621 GCST90248848 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein arginine N-methyltransferase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein arginine N-methyltransferase 3 measurement http://www.ebi.ac.uk/efo/EFO_0802925 GCST90248849 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oxysterols receptor LXR-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 oxysterols receptor LXR-beta measurement http://www.ebi.ac.uk/efo/EFO_0801865 GCST90248809 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Oxytocin-neurophysin 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 oxytocin-neurophysin 1 measurement http://www.ebi.ac.uk/efo/EFO_0802839 GCST90248810 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Paired immunoglobulin-like type 2 receptor alpha isoform FDF03-deltaTM levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248811 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Paired immunoglobulin-like type 2 receptor alpha isoform FDF03-M14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248812 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. General vesicular transport factor p115 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248813 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Actin-related protein 2/3 complex subunit 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248814 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear pore membrane glycoprotein 210-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 nuclear pore membrane glycoprotein 210-like measurement http://www.ebi.ac.uk/efo/EFO_0802821 GCST90248815 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fragile X mental retardation protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247625 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fms-related tyrosine kinase 3 ligand levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90247626 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibronectin type III domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibronectin type III domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802549 GCST90247627 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Folate receptor beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247628 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Folate receptor gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247629 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Forkhead box protein C2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 forkhead box protein C2 measurement http://www.ebi.ac.uk/efo/EFO_0802553 GCST90247630 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Forkhead box protein G1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247631 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Forkhead box protein J2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 forkhead box protein J2 measurement http://www.ebi.ac.uk/efo/EFO_0801604 GCST90247632 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Forkhead box protein M1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247633 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Forkhead box protein O3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247634 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fractalkine levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 fractalkine measurement http://www.ebi.ac.uk/efo/EFO_0020395 GCST90247635 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Frizzled-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247636 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Follicle stimulating hormone levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90247637 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Follistatin-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 follistatin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021934 GCST90247638 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Follistatin-related protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 follistatin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020394 GCST90247639 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Follistatin-related protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 follistatin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801603 GCST90247640 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibronectin type 3 and ankyrin repeat domains protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247641 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Formimidoyltransferase-cyclodeaminase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 formimidoyltransferase-cyclodeaminase measurement http://www.ebi.ac.uk/efo/EFO_0021895 GCST90247642 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ferritin, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247643 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fumarate hydratase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247644 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Furin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 furin measurement http://www.ebi.ac.uk/efo/EFO_0801610 GCST90247645 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-(1,3)-fucosyltransferase 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 alpha-(1,3)-fucosyltransferase 10 measurement http://www.ebi.ac.uk/efo/EFO_0801366 GCST90247646 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-(1,3)-fucosyltransferase 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 alpha-(1,3)-fucosyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020136 GCST90247647 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-(1,6)-fucosyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-(1,6)-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0801368 GCST90247648 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-(1,3)-fucosyltransferase 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-(1,3)-fucosyltransferase 9 measurement http://www.ebi.ac.uk/efo/EFO_0801367 GCST90247649 Genome-wide genotyping array 2023-05-23 37165452 Zhu C 2023-05-10 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/37165452 Genetic basis of STEM occupational choice and regional economic performance: a UK biobank genome-wide association study. Science, technology, engineering or mathematics occupational choice 9,273 British ancestry cases, 169,703 British ancestry controls NA Affymetrix [7677418] (imputed) 2 employment status http://www.ebi.ac.uk/efo/EFO_0005241 GCST90269769 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5-hydroxytryptamine receptor 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246380 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5-hydroxytryptamine receptor 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246381 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5-Nucleotidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246382 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 6-phosphogluconolactonase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246383 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 6-phosphogluconate dehydrogenase, decarboxylating levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 6-phosphogluconate dehydrogenase, decarboxylating measurement http://www.ebi.ac.uk/efo/EFO_0020120 GCST90246384 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 7-methylguanosine phosphate-specific 5-nucleotidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246385 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 7,8-dihydro-8-oxoguanine triphosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246386 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-crystallin A chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-crystallin A chain measurement http://www.ebi.ac.uk/efo/EFO_0802267 GCST90246387 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1-antichymotrypsin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-1-antichymotrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008019 GCST90246388 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. alpha-1-antichymotrypsin complex levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 alpha-1-antichymotrypsin complex measurement http://www.ebi.ac.uk/efo/EFO_0008018 GCST90246389 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1-antitrypsin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008327 GCST90246390 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1B-glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246391 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. APOBEC1 complementation factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 APOBEC1 complementation factor measurement http://www.ebi.ac.uk/efo/EFO_0801386 GCST90246392 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1-microglobulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246393 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1-syntrophin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246394 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-2-antiplasmin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 alpha-2-antiplasmin measurement http://www.ebi.ac.uk/efo/EFO_0020137 GCST90246395 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-2-HS-glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90246396 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-2-macroglobulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 alpha-2-macroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020138 GCST90246397 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-2-macroglobulin-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246398 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1,4-N-acetylglucosaminyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246399 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent 6-phosphofructokinase, muscle type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246400 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-amylase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 alpha-amylase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801371 GCST90246401 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-amylase 2B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246402 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aflatoxin B1 aldehyde reductase member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 aflatoxin B1 aldehyde reductase member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020132 GCST90246403 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Aflatoxin B1 aldehyde reductase member 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90246404 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor receptor substrate 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247600 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibrinogen-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247601 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor receptor-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247602 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bis(5-adenosyl)-triphosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247603 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibronectin Fragment 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibronectin fragment 3 measurement http://www.ebi.ac.uk/efo/EFO_0008131 GCST90247604 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acidic fibroblast growth factor intracellular-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247605 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibrinogen levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90247606 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibrinogen beta chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247607 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibrinogen C domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibrinogen C domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802548 GCST90247608 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibrinogen gamma chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibrinogen gamma chain measurement http://www.ebi.ac.uk/efo/EFO_0020374 GCST90247609 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroleukin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247610 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. fibromodulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247611 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibulin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fibulin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802550 GCST90247612 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibulin-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247613 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ficolin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90247614 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ficolin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 ficolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008135 GCST90247615 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ficolin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 ficolin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020392 GCST90247616 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Four-jointed box protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 four-jointed box protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801605 GCST90247617 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inactive peptidyl-prolyl cis-trans isomerase FKBP6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 inactive peptidyl-prolyl cis-trans isomerase FKBP6 measurement http://www.ebi.ac.uk/efo/EFO_0801694 GCST90247618 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein flightless-1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247619 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ferritin light chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247620 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat transmembrane protein FLRT1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 leucine-rich repeat transmembrane protein FLRT1 measurement http://www.ebi.ac.uk/efo/EFO_0020533 GCST90247621 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat transmembrane protein FLRT2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 leucine-rich repeat transmembrane protein FLRT2 measurement http://www.ebi.ac.uk/efo/EFO_0021860 GCST90247622 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leucine-rich repeat transmembrane protein FLRT3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90247623 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor-type tyrosine-protein kinase FLT3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 receptor-type tyrosine-protein kinase flt3 measurement http://www.ebi.ac.uk/efo/EFO_0020703 GCST90247624 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chymotrypsin-like elastase family member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247434 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chymotrypsin-like elastase family member 2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 chymotrypsin-like elastase family member 2A measurement http://www.ebi.ac.uk/efo/EFO_0802399 GCST90247435 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Elafin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90247436 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ELAV-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ELAV-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801562 GCST90247437 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ETS-related transcription factor Elf-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ETS-related transcription factor Elf-5 measurement http://www.ebi.ac.uk/efo/EFO_0802534 GCST90247438 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ETS domain-containing protein Elk-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ETS domain-containing protein Elk-1 measurement http://www.ebi.ac.uk/efo/EFO_0801587 GCST90247439 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ETS domain-containing protein Elk-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ETS domain-containing protein Elk-3 measurement http://www.ebi.ac.uk/efo/EFO_0801588 GCST90247440 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Engulfment and cell motility protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 engulfment and cell motility protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802522 GCST90247441 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelial monocyte-activating polypeptide 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 endothelial monocyte-activating polypeptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020348 GCST90247442 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ER membrane protein complex subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ER membrane protein complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0801579 GCST90247443 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ER membrane protein complex subunit 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ER membrane protein complex subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0801580 GCST90247444 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ER membrane protein complex subunit 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247445 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EMILIN-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 EMILIN-3 measurement http://www.ebi.ac.uk/efo/EFO_0801563 GCST90247446 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adhesion G protein-coupled receptor E2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 adhesion G protein-coupled receptor E2 measurement http://www.ebi.ac.uk/efo/EFO_0021892 GCST90247447 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelial cell-specific molecule 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 endothelial cell-specific molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010912 GCST90247448 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoglin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 endoglin measurement http://www.ebi.ac.uk/efo/EFO_0008118 GCST90247449 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endophilin-A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247450 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endophilin-A3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247451 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endophilin-B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247452 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endophilin-B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247453 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoplasmin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 endoplasmin measurement http://www.ebi.ac.uk/efo/EFO_0801570 GCST90247454 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endosialin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247455 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endostatin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 endostatin measurement http://www.ebi.ac.uk/efo/EFO_0020347 GCST90247456 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247457 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 endothelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801572 GCST90247458 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247459 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ecto-NOX disulfide-thiol exchanger 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247460 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ecto-NOX disulfide-thiol exchanger 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ecto-NOX disulfide-thiol exchanger 2 measurement http://www.ebi.ac.uk/efo/EFO_0802516 GCST90247461 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247462 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleotide pyrophosphatase/phosphodiesterase family member 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ectonucleotide pyrophosphatase/phosphodiesterase family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0801560 GCST90247463 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleotide pyrophosphatase/phosphodiesterase family member 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247464 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0020344 GCST90247465 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleoside triphosphate diphosphohydrolase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90247466 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleoside triphosphate diphosphohydrolase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ectonucleoside triphosphate diphosphohydrolase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020343 GCST90247467 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleoside triphosphate diphosphohydrolase 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90247468 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectonucleoside triphosphate diphosphohydrolase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ectonucleoside triphosphate diphosphohydrolase 6 measurement http://www.ebi.ac.uk/efo/EFO_0802517 GCST90247469 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eotaxin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90247470 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-A receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ephrin type-A receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008123 GCST90247471 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-A receptor 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ephrin type-a receptor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020350 GCST90247472 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-A receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ephrin type-a receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020351 GCST90247473 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-A receptor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ephrin type-a receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020352 GCST90247474 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-A receptor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247475 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-A receptor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ephrin type-a receptor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020353 GCST90247476 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-A receptor 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247477 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-B receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247478 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-B receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90247479 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-B receptor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ephrin type-B receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0801574 GCST90247480 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-B receptor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ephrin type-b receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020354 GCST90247481 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin type-B receptor 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90247482 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epiregulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 epiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020361 GCST90247483 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epidermal growth factor receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90247409 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epidermal growth factor receptor substrate 15-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 epidermal growth factor receptor substrate 15-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020360 GCST90247410 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epidermal growth factor receptor variant III levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247411 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Egl nine homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247412 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EH domain-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 EH domain-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801561 GCST90247413 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EH domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 EH domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802519 GCST90247414 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase EHMT2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 histone-lysine n-methyltransferase EHMT2 measurement http://www.ebi.ac.uk/efo/EFO_0020455 GCST90247415 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic initiation factor 4A-I levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247416 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic initiation factor 4A-II levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247417 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic initiation factor 4A-III levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 eukaryotic initiation factor 4a-III measurement http://www.ebi.ac.uk/efo/EFO_0020366 GCST90247418 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable RNA-binding protein EIF1AD levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 probable RNA-binding protein EIF1AD measurement http://www.ebi.ac.uk/efo/EFO_0801918 GCST90247419 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 1b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247420 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 2 subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247421 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 3 subunit G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 eukaryotic translation initiation factor 3 subunit G measurement http://www.ebi.ac.uk/efo/EFO_0801590 GCST90247422 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 3 subunit J levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 eukaryotic translation initiation factor 3 subunit J measurement http://www.ebi.ac.uk/efo/EFO_0801591 GCST90247423 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 4B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 eukaryotic translation initiation factor 4B measurement http://www.ebi.ac.uk/efo/EFO_0801592 GCST90247424 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 4E levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247425 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 4E-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 eukaryotic translation initiation factor 4E-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020368 GCST90247426 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 4E type 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 eukaryotic translation initiation factor 4E type 2 measurement http://www.ebi.ac.uk/efo/EFO_0801593 GCST90247427 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 4 gamma 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 eukaryotic translation initiation factor 4 gamma 2 measurement http://www.ebi.ac.uk/efo/EFO_0020367 GCST90247428 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 4 gamma 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 eukaryotic translation initiation factor 4 gamma 3 measurement http://www.ebi.ac.uk/efo/EFO_0802535 GCST90247429 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 4H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 eukaryotic translation initiation factor 4H measurement http://www.ebi.ac.uk/efo/EFO_0021999 GCST90247430 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 eukaryotic translation initiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020369 GCST90247431 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 5A-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 eukaryotic translation initiation factor 5A-1 measurement http://www.ebi.ac.uk/efo/EFO_0020370 GCST90247432 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 5A-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247433 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoplasmic reticulum lectin 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 endoplasmic reticulum lectin 1 measurement http://www.ebi.ac.uk/efo/EFO_0801567 GCST90247484 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-hydroxyacyl-CoA dehydrogenase type-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 3-hydroxyacyl-coa dehydrogenase type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020114 GCST90247485 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoplasmic reticulum aminopeptidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90247486 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoplasmic reticulum aminopeptidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 endoplasmic reticulum aminopeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801566 GCST90247487 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor tyrosine-protein kinase erbB-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 receptor tyrosine-protein kinase erbb-3 measurement http://www.ebi.ac.uk/efo/EFO_0020701 GCST90247488 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Receptor tyrosine-protein kinase erbB-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 receptor tyrosine-protein kinase erbb-4 measurement http://www.ebi.ac.uk/efo/EFO_0020702 GCST90247489 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA excision repair protein ERCC-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DNA excision repair protein ERCC-1 measurement http://www.ebi.ac.uk/efo/EFO_0802474 GCST90247490 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein ERGIC-53 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247491 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Erlin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 erlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801581 GCST90247492 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ERO1-like protein alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ERO1-like protein alpha measurement http://www.ebi.ac.uk/efo/EFO_0801582 GCST90247493 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ERO1-like protein beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ERO1-like protein beta measurement http://www.ebi.ac.uk/efo/EFO_0801583 GCST90247494 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoplasmic reticulum resident protein 29 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 endoplasmic reticulum resident protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0020346 GCST90247495 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoplasmic reticulum resident protein 44 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 endoplasmic reticulum resident protein 44 measurement http://www.ebi.ac.uk/efo/EFO_0801569 GCST90247496 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endogenous retrovirus group V member 1 Env polyprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 endogenous retrovirus group V member 1 Env polyprotein measurement http://www.ebi.ac.uk/efo/EFO_0801565 GCST90247497 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Erythrocyte band 7 integral membrane protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 erythrocyte band 7 integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801584 GCST90247498 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Erythroid membrane-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 erythroid membrane-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801585 GCST90247499 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Erythropoietin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 erythropoietin measurement http://www.ebi.ac.uk/efo/EFO_0020363 GCST90247500 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ES1 protein homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ES1 protein homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802529 GCST90247501 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epididymis-specific alpha-mannosidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 epididymis-specific alpha-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801577 GCST90247502 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Electroneutral sodium bicarbonate exchanger 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 electroneutral sodium bicarbonate exchanger 1 measurement http://www.ebi.ac.uk/efo/EFO_0802520 GCST90247503 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E-selectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90247504 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epididymal-specific lipocalin-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 epididymal-specific lipocalin-10 measurement http://www.ebi.ac.uk/efo/EFO_0801576 GCST90247505 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epididymal-specific lipocalin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 epididymal-specific lipocalin-8 measurement http://www.ebi.ac.uk/efo/EFO_0802528 GCST90247506 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epididymal secretory protein E3-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 epididymal secretory protein E3-beta measurement http://www.ebi.ac.uk/efo/EFO_0802527 GCST90247507 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epithelial splicing regulatory protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247508 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM24B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein FAM24B measurement http://www.ebi.ac.uk/efo/EFO_0802944 GCST90247534 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247535 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAX gene-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 MAX gene-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0801790 GCST90248426 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAX-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 MAX-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802732 GCST90248427 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myc-associated zinc finger protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 myc-associated zinc finger protein measurement http://www.ebi.ac.uk/efo/EFO_0802766 GCST90248428 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mannan-binding lectin serine protease 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90248429 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Membrane-bound transcription factor site-1 protease levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248430 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myeloid cell surface antigen CD33 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90248431 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mast cell-expressed membrane protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 mast cell-expressed membrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801787 GCST90248432 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Induced myeloid leukemia cell differentiation protein Mcl-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 induced myeloid leukemia cell differentiation protein Mcl-1 measurement http://www.ebi.ac.uk/efo/EFO_0021910 GCST90248433 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Malonyl-CoA decarboxylase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 malonyl-CoA decarboxylase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802727 GCST90248434 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methylmalonyl-CoA epimerase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 methylmalonyl-CoA epimerase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802742 GCST90248435 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Membrane cofactor protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248436 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mineralocorticoid receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 mineralocorticoid receptor measurement http://www.ebi.ac.uk/efo/EFO_0801802 GCST90248437 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage colony-stimulating factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 macrophage colony-stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020546 GCST90248438 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage colony-stimulating factor 1 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 macrophage colony-stimulating factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020547 GCST90248439 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAM domain-containing glycosylphosphatidylinositol anchor protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248440 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAM domain-containing glycosylphosphatidylinositol anchor protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248441 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myeloid-derived growth factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248442 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. melanoma-derived growth regulatory protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90248443 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Mdm4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248444 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myocyte-specific enhancer factor 2C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 myocyte-specific enhancer factor 2C measurement http://www.ebi.ac.uk/efo/EFO_0802770 GCST90248445 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Multiple epidermal growth factor-like domains protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 multiple epidermal growth factor-like domains protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0802762 GCST90248446 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein MEMO1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248447 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein MENT levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein MENT measurement http://www.ebi.ac.uk/efo/EFO_0801952 GCST90248448 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Estradiol 17-beta-dehydrogenase 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247509 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Estradiol 17-beta-dehydrogenase 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247510 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Estrogen sulfotransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 estrogen sulfotransferase measurement http://www.ebi.ac.uk/efo/EFO_0801586 GCST90247511 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 1A, X-chromosomal levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 eukaryotic translation initiation factor 1A, X-chromosomal measurement http://www.ebi.ac.uk/efo/EFO_0801589 GCST90247512 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic translation initiation factor 1A, Y-chromosomal levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247513 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Electron transfer flavoprotein subunit alpha, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247514 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Persulfide dioxygenase ETHE1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 persulfide dioxygenase ETHE1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008258 GCST90247515 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein C-ets-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein C-ets-2 measurement http://www.ebi.ac.uk/efo/EFO_0801935 GCST90247516 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ETS translocation variant 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247517 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ena/VASP-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 Ena/VASP-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801564 GCST90247518 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Exostosin-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 exostosin-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801595 GCST90247519 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ezrin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ezrin measurement http://www.ebi.ac.uk/efo/EFO_0801597 GCST90247520 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM107A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein fam107a measurement http://www.ebi.ac.uk/efo/EFO_0020673 GCST90247521 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM134B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein FAM134B measurement http://www.ebi.ac.uk/efo/EFO_0802935 GCST90247522 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM151A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein FAM151A measurement http://www.ebi.ac.uk/efo/EFO_0801945 GCST90247523 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM162A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247524 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM163B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein FAM163B measurement http://www.ebi.ac.uk/efo/EFO_0802936 GCST90247525 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fructose-1,6-bisphosphatase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fructose-1,6-bisphosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801606 GCST90247526 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fructose-1,6-bisphosphatase isozyme 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 fructose-1,6-bisphosphatase isozyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0802556 GCST90247527 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM171B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein FAM171B measurement http://www.ebi.ac.uk/efo/EFO_0801947 GCST90247528 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM172A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein FAM172A measurement http://www.ebi.ac.uk/efo/EFO_0802937 GCST90247529 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM177A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein FAM177A1 measurement http://www.ebi.ac.uk/efo/EFO_0801948 GCST90247530 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM19A5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein FAM19A5 measurement http://www.ebi.ac.uk/efo/EFO_0802942 GCST90247531 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM209B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein FAM209B measurement http://www.ebi.ac.uk/efo/EFO_0802943 GCST90247532 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM234B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247533 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Muellerian-inhibiting factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 muellerian-inhibiting factor measurement http://www.ebi.ac.uk/efo/EFO_0020584 GCST90248474 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Allergin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 allergin-1 measurement http://www.ebi.ac.uk/efo/EFO_0801365 GCST90248475 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mimecan levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248476 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Multiple inositol polyphosphate phosphatase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 multiple inositol polyphosphate phosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801811 GCST90248477 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAP kinase-activated protein kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 MAP kinase-activated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008225 GCST90248478 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAP kinase-activated protein kinase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90248479 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAP kinase-activated protein kinase 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 MAP kinase-activated protein kinase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020553 GCST90248480 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myeloid leukemia factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248481 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myosin regulatory light chain 2, atrial isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248482 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248483 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitotic spindle assembly checkpoint protein MAD1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 mitotic spindle assembly checkpoint protein MAD1 measurement http://www.ebi.ac.uk/efo/EFO_0801807 GCST90248484 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitotic spindle assembly checkpoint protein MAD2A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248485 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Membrane magnesium transporter 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 membrane magnesium transporter 1 measurement http://www.ebi.ac.uk/efo/EFO_0802736 GCST90248486 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage Migration Inhibitory Factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST90248487 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix metalloproteinase-14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 matrix metalloproteinase-14 measurement http://www.ebi.ac.uk/efo/EFO_0020558 GCST90248488 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix metalloproteinase-16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 matrix metalloproteinase-16 measurement http://www.ebi.ac.uk/efo/EFO_0020559 GCST90248489 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix metalloproteinase-17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 matrix metalloproteinase-17 measurement http://www.ebi.ac.uk/efo/EFO_0020560 GCST90248490 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix metalloproteinase-19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248491 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 72 kDa type IV collagenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248492 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix metalloproteinase-20 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248493 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix metalloproteinase-9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 matrix metalloproteinase-9 measurement http://www.ebi.ac.uk/efo/EFO_0020561 GCST90248494 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage mannose receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 macrophage mannose receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020548 GCST90248495 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248496 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage metalloelastase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 macrophage metalloelastase measurement http://www.ebi.ac.uk/efo/EFO_0008220 GCST90248497 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mortality factor 4-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248498 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homeobox protein MOX-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248449 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix extracellular phosphoglycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 matrix extracellular phosphoglycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020557 GCST90248450 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. LDLR chaperone MESD levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 LDLR chaperone MESD measurement http://www.ebi.ac.uk/efo/EFO_0802686 GCST90248451 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methyltransferase-like protein 24 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248452 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metaxin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248453 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methyl-CpG-binding domain protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248454 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitochondrial fission 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248455 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microfibril-associated glycoprotein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 microfibril-associated glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802744 GCST90248456 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Membrane protein FAM174A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 membrane protein FAM174A measurement http://www.ebi.ac.uk/efo/EFO_0801795 GCST90248457 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microfibrillar-associated protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 microfibrillar-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801801 GCST90248458 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microfibrillar-associated protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 microfibrillar-associated protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802746 GCST90248459 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Beta-1,3-N-acetylglucosaminyltransferase manic fringe levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 beta-1,3-N-acetylglucosaminyltransferase manic fringe measurement http://www.ebi.ac.uk/efo/EFO_0802311 GCST90248460 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802263 GCST90248461 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0801370 GCST90248462 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix Gla protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248463 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein mago nashi homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248464 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248465 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B measurement http://www.ebi.ac.uk/efo/EFO_0801369 GCST90248466 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C measurement http://www.ebi.ac.uk/efo/EFO_0802264 GCST90248467 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MHC class I polypeptide-related sequence A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST90248468 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MHC class I polypeptide-related sequence B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 MHC class I polypeptide-related sequence B measurement http://www.ebi.ac.uk/efo/EFO_0008234 GCST90248469 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MICOS complex subunit MIC10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 MICOS complex subunit MIC10 measurement http://www.ebi.ac.uk/efo/EFO_0801800 GCST90248470 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MICAL-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 MICAL-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801799 GCST90248471 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable E3 ubiquitin-protein ligase MID2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 probable E3 ubiquitin-protein ligase MID2 measurement http://www.ebi.ac.uk/efo/EFO_0802904 GCST90248472 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Midkine levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 midkine measurement http://www.ebi.ac.uk/efo/EFO_0020571 GCST90248473 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myeloperoxidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90248549 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myeloblastin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90248550 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myosin light chain 6B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248551 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myosin light chain 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248552 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myosin light chain 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248553 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AMSH-like protease levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 AMSH-like protease measurement http://www.ebi.ac.uk/efo/EFO_0802274 GCST90249671 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal-transducing adaptor protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 signal-transducing adaptor protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803075 GCST90249672 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. StAR-related lipid transfer protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249673 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Statherin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249674 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal transducer and activator of transcription 1-alpha/beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 signal transducer and activator of transcription 1-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0021915 GCST90249675 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal transducer and activator of transcription 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 signal transducer and activator of transcription 3 measurement http://www.ebi.ac.uk/efo/EFO_0021907 GCST90249676 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Signal transducer and activator of transcription 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 signal transducer and activator of transcription 6 measurement http://www.ebi.ac.uk/efo/EFO_0021916 GCST90249677 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stromal interaction molecule 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 stromal interaction molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0802093 GCST90249678 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 serine/threonine-protein kinase 16 measurement http://www.ebi.ac.uk/efo/EFO_0020724 GCST90249679 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase 17B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine/threonine-protein kinase 17B measurement http://www.ebi.ac.uk/efo/EFO_0008281 GCST90249680 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase A-Raf levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249681 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase BRSK2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 serine/threonine-protein kinase BRSK2 measurement http://www.ebi.ac.uk/efo/EFO_0803063 GCST90249682 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase B-raf levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249683 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase Chk1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 serine/threonine-protein kinase Chk1 measurement http://www.ebi.ac.uk/efo/EFO_0021965 GCST90249684 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase Chk2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein kinase CHK2 measurement http://www.ebi.ac.uk/efo/EFO_0020726 GCST90249685 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase DCLK1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249686 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase DCLK3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein kinase DCLK3 measurement http://www.ebi.ac.uk/efo/EFO_0803064 GCST90249687 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase/endoribonuclease IRE1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249688 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase N1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249689 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase Nek7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249690 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MOB-like protein phocein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248499 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adenylyltransferase and sulfurtransferase MOCS3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 adenylyltransferase and sulfurtransferase MOCS3 measurement http://www.ebi.ac.uk/efo/EFO_0802257 GCST90248500 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Moesin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248501 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myelin-oligodendrocyte glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248502 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Monocarboxylate transporter 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248503 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAGUK p55 subfamily member 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 MAGUK p55 subfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0801781 GCST90248504 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAGUK p55 subfamily member 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 MAGUK p55 subfamily member 7 measurement http://www.ebi.ac.uk/efo/EFO_0802724 GCST90248505 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mannose-binding protein C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 mannose-binding protein C measurement http://www.ebi.ac.uk/efo/EFO_0008224 GCST90248506 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Multiple PDZ domain protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 multiple PDZ domain protein measurement http://www.ebi.ac.uk/efo/EFO_0802763 GCST90248507 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metalloproteinase inhibitor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 metalloproteinase inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020566 GCST90248508 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metalloproteinase inhibitor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 metalloproteinase inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020567 GCST90248509 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metalloproteinase inhibitor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 metalloproteinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008231 GCST90248510 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metalloproteinase inhibitor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 metalloproteinase inhibitor 4 measurement http://www.ebi.ac.uk/efo/EFO_0801797 GCST90248511 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. M-phase inducer phosphatase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 m-phase inducer phosphatase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801780 GCST90248512 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Metallophosphoesterase MPPED2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248513 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myelin protein zero-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248514 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myelin protein zero-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248515 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type mannose receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 C-type mannose receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020204 GCST90248516 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Double-strand break repair protein MRE11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248517 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanoregulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248518 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myelin regulatory factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 myelin regulatory factor measurement http://www.ebi.ac.uk/efo/EFO_0802767 GCST90248519 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. mRNA-capping enzyme levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 MRNA-capping enzyme measurement http://www.ebi.ac.uk/efo/EFO_0802756 GCST90248520 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. mRNA-decapping enzyme 1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 MRNA-decapping enzyme 1A measurement http://www.ebi.ac.uk/efo/EFO_0802757 GCST90248521 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. mRNA-decapping enzyme 1B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248522 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mediator of RNA polymerase II transcription subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90248523 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mediator of RNA polymerase II transcription subunit 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 mediator of RNA polymerase II transcription subunit 4 measurement http://www.ebi.ac.uk/efo/EFO_0801791 GCST90248524 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Multidrug resistance-associated protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 multidrug resistance-associated protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0802760 GCST90248525 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methionine-R-sulfoxide reductase B2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248526 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methionine-R-sulfoxide reductase B3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 methionine-R-sulfoxide reductase B3 measurement http://www.ebi.ac.uk/efo/EFO_0802741 GCST90248527 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein MRVI1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein MRVI1 measurement http://www.ebi.ac.uk/efo/EFO_0801953 GCST90248528 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA mismatch repair protein Msh2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248529 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Malignant T-cell-amplified sequence 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 malignant T-cell-amplified sequence 1 measurement http://www.ebi.ac.uk/efo/EFO_0801782 GCST90248530 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein p13 MTCP-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein p13 MTCP-1 measurement http://www.ebi.ac.uk/efo/EFO_0802955 GCST90248531 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248532 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitochondrial fission regulator 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 mitochondrial fission regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0802749 GCST90248533 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 5-formyltetrahydrofolate cyclo-ligase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 5-formyltetrahydrofolate cyclo-ligase measurement http://www.ebi.ac.uk/efo/EFO_0801335 GCST90248534 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248535 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myotubularin-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 myotubularin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802773 GCST90248536 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myotubularin-related protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248537 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methenyltetrahydrofolate synthase domain-containing protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248538 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mucin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90248539 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mucin-16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248540 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mucin-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248541 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Multimerin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 multimerin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801809 GCST90248542 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mevalonate kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248543 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Interferon-induced GTP-binding protein Mx1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248544 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix-remodeling-associated protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 matrix-remodeling-associated protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0801789 GCST90248545 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrix-remodeling-associated protein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 matrix-remodeling-associated protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0802731 GCST90248546 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myc box-dependent-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 myc box-dependent-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802765 GCST90248547 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myc target protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 myc target protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801812 GCST90248548 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stromelysin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 stromelysin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802095 GCST90249716 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 syntaxin-10 measurement http://www.ebi.ac.uk/efo/EFO_0802110 GCST90249717 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249718 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-1A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 syntaxin-1a measurement http://www.ebi.ac.uk/efo/EFO_0020759 GCST90249719 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 syntaxin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802111 GCST90249720 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249721 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249722 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 syntaxin-7 measurement http://www.ebi.ac.uk/efo/EFO_0802112 GCST90249723 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 syntaxin-8 measurement http://www.ebi.ac.uk/efo/EFO_0802113 GCST90249724 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Syntaxin-binding protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249725 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Suppressor of fused homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249726 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein SGT1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249727 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Extracellular sulfatase Sulf-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 extracellular sulfatase Sulf-2 measurement http://www.ebi.ac.uk/efo/EFO_0801596 GCST90249728 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfhydryl oxidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 sulfhydryl oxidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802100 GCST90249729 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfatase-modifying factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 sulfatase-modifying factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802098 GCST90249730 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfatase-modifying factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249731 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small ubiquitin-related modifier 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249732 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Small ubiquitin-related modifier 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 small ubiquitin-related modifier 3 measurement http://www.ebi.ac.uk/efo/EFO_0022025 GCST90249733 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SUN domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 SUN domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802102 GCST90249734 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. SUN domain-containing protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 SUN domain-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802103 GCST90249735 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sulfite oxidase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249736 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Surfeit locus protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 surfeit locus protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802105 GCST90249737 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sushi domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 Sushi domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803111 GCST90249738 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Sushi domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 Sushi domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803112 GCST90249739 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase SUV420H2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 histone-lysine N-methyltransferase SUV420H2 measurement http://www.ebi.ac.uk/efo/EFO_0802606 GCST90249740 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase PAK 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 serine/threonine-protein kinase PAK 3 measurement http://www.ebi.ac.uk/efo/EFO_0020728 GCST90249691 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase PAK 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249692 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase PAK 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 serine/threonine-protein kinase PAK 6 measurement http://www.ebi.ac.uk/efo/EFO_0020729 GCST90249693 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase pim-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein kinase PIM-1 measurement http://www.ebi.ac.uk/efo/EFO_0020731 GCST90249694 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase PLK1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein kinase PLK1 measurement http://www.ebi.ac.uk/efo/EFO_0020732 GCST90249695 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase receptor R3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine/threonine-protein kinase receptor R3 measurement http://www.ebi.ac.uk/efo/EFO_0020733 GCST90249696 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase Sgk3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249697 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase TBK1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein kinase TBK1 measurement http://www.ebi.ac.uk/efo/EFO_0020734 GCST90249698 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase ULK3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 serine/threonine-protein kinase ULK3 measurement http://www.ebi.ac.uk/efo/EFO_0803065 GCST90249699 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase VRK1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein kinase VRK1 measurement http://www.ebi.ac.uk/efo/EFO_0803066 GCST90249700 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase WNK3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine/threonine-protein kinase WNK3 measurement http://www.ebi.ac.uk/efo/EFO_0021992 GCST90249701 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stomatin-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249702 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stomatin-like protein 2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249703 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stathmin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249704 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stathmin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 stathmin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802087 GCST90249705 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stathmin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 stathmin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802088 GCST90249706 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase MRCK alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 serine/threonine-protein kinase MRCK alpha measurement http://www.ebi.ac.uk/efo/EFO_0802058 GCST90249707 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein kinase MRCK beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein kinase MRCK beta measurement http://www.ebi.ac.uk/efo/EFO_0020727 GCST90249708 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein phosphatase 4 regulatory subunit 3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249709 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform measurement http://www.ebi.ac.uk/efo/EFO_0803067 GCST90249710 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein phosphatase 2A regulatory subunit B subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249711 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine/threonine-protein phosphatase PP1-gamma catalytic subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249712 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Serine--tRNA ligase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 serine--tRNA ligase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0803061 GCST90249713 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Somatotropin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249714 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Stromelysin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249715 Genome-wide genotyping array 2023-09-28 37709864 Chen Y 2023-09-14 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37709864 Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease. Nonalcoholic fatty liver disease 691,479 European ancestry, African American or Afro-Caribbean, East Asian ancestry, Hispanic or Latin American, South Asian ancestry individuals NA NR [10696387] (imputed) 17 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90271622 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Erythrocyte sedimentation rate x secukinumab treatment interaction in ankylosing spondylitis 117 admixed American ancestry individuals, 632 European ancestry individuals, 5 East Asian ancestry, South Asian ancestry, African ancestry individuals NA Illumina [4248237] (imputed) 0 blood sedimentation, response to secukinumab http://www.ebi.ac.uk/efo/EFO_0004304, http://www.ebi.ac.uk/efo/EFO_0022378 GCST90274736 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. C-reactive protein levels x secukinumab treatment interaction in inflammatory disease 739 admixed American ancestry individuals, 4,106 European ancestry individuals, 373 East Asian ancestry, South Asian ancestry, African ancestry individuals NA Illumina [4972932] (imputed) 0 response to secukinumab, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0004458 GCST90274737 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Ankylosing spondylitis disease activity score with CRP x secukinumab treatment interaction in ankylosing spondylitis 117 admixed American ancestry individuals, 632 European ancestry individuals, 5 East Asian ancestry, South Asian ancestry, African ancestry individuals NA Illumina [4247422] (imputed) 0 response to secukinumab, ankylosing spondylitis disease activity score, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0022377, http://www.ebi.ac.uk/efo/EFO_0004458 GCST90274734 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Disease activity-28 score with CRP x secukinumab treatment interaction in psoriatic arthritis 200 admixed American ancestry individuals, 1,741 European ancestry individuals, 17 East Asian ancestry individuals, 48 South Asian ancestry individuals NA Illumina [4488859] (imputed) 0 response to secukinumab, C-reactive protein measurement, arthritis disease activity score measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0009435 GCST90274739 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. C-reactive protein levels x secukinumab treatment interaction in ankylosing spondylitis 117 admixed American ancestry individuals, 632 European ancestry individuals, 5 East Asian ancestry, South Asian ancestry, African ancestry individuals NA Illumina [4250425] (imputed) 0 response to secukinumab, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0004458 GCST90274735 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Erythrocyte sedimentation rate x secukinumab treatment interaction in inflammatory disease 739 admixed American ancestry individuals, 4,106 European ancestry individuals, 373 East Asian ancestry, South Asian ancestry, African ancestry individuals NA Illumina [4934518] (imputed) 0 blood sedimentation, response to secukinumab http://www.ebi.ac.uk/efo/EFO_0004304, http://www.ebi.ac.uk/efo/EFO_0022378 GCST90274738 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. American College of Rheumatology Improvement Criteria x secukinumab treatment interaction in psoriatic arthritis 200 admixed American ancestry individuals, 1,741 European ancestry individuals, 17 East Asian ancestry individuals, 48 South Asian ancestry individuals NA Illumina [4496106] (imputed) 0 American College of Rheumatology Improvement Criteria, response to secukinumab http://www.ebi.ac.uk/efo/EFO_0022379, http://www.ebi.ac.uk/efo/EFO_0022378 GCST90274740 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. C-reactive protein levels x secukinumab treatment interaction in psoriatic arthritis 200 admixed American ancestry individuals, 1,741 European ancestry individuals, 17 East Asian ancestry individuals, 48 South Asian ancestry individuals NA Illumina [4490035] (imputed) 0 response to secukinumab, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0004458 GCST90274741 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Erythrocyte sedimentation rate x secukinumab treatment interaction in psoriatic arthritis 200 admixed American ancestry individuals, 1,741 European ancestry individuals, 17 East Asian ancestry individuals, 48 South Asian ancestry individuals NA Illumina [4488024] (imputed) 0 blood sedimentation, response to secukinumab http://www.ebi.ac.uk/efo/EFO_0004304, http://www.ebi.ac.uk/efo/EFO_0022378 GCST90274742 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Health Assessment Questionnaire Disability Index x secukinumab treatment interaction in psoriatic arthritis 200 admixed American ancestry individuals, 1,741 European ancestry individuals, 17 East Asian ancestry individuals, 48 South Asian ancestry individuals NA Illumina [4488277] (imputed) 0 response to secukinumab, Health Assessment Questionnaire Disability Index http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0022381 GCST90274743 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Swollen Joint Count 76 x secukinumab treatment interaction in psoriatic arthritis 200 admixed American ancestry individuals, 1,741 European ancestry individuals, 17 East Asian ancestry individuals, 48 South Asian ancestry individuals NA Illumina [4488271] (imputed) 0 response to secukinumab, joint damage measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0005413 GCST90274744 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. C-reactive protein levels x secukinumab treatment interaction in psoriasis 229 admixed American ancestry individuals, 1,234 European ancestry individuals, 77 East Asian ancestry individuals, 86 South Asian ancestry individuals NA Illumina [4566562] (imputed) 0 response to secukinumab, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0004458 GCST90274745 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Psoriasis area and severity index x secukinumab treatment interaction in psoriasis 229 admixed American ancestry individuals, 1,234 European ancestry individuals, 77 East Asian ancestry individuals, 86 South Asian ancestry individuals NA Illumina [4549290] (imputed) 0 response to secukinumab, psoriasis area and severity index http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0022382 GCST90274746 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. American College of Rheumatology Improvement Criteria x secukinumab treatment interaction in rheumatoid arthritis 193 admixed American ancestry individuals, 499 European ancestry individuals, 110 East Asian ancestry individuals, 17 South Asian ancestry individuals, 3 African ancestry individuals NA Illumina [4822933] (imputed) 0 American College of Rheumatology Improvement Criteria, response to secukinumab http://www.ebi.ac.uk/efo/EFO_0022379, http://www.ebi.ac.uk/efo/EFO_0022378 GCST90274747 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. C-reactive protein levels x secukinumab treatment interaction in rheumatoid arthritis 193 admixed American ancestry individuals, 499 European ancestry individuals, 110 East Asian ancestry individuals, 17 South Asian ancestry individuals, 3 African ancestry individuals NA Illumina [4840377] (imputed) 0 response to secukinumab, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0004458 GCST90274748 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Disease activity-28 score with CRP x secukinumab treatment interaction in rheumatoid arthritis 193 admixed American ancestry individuals, 499 European ancestry individuals, 110 East Asian ancestry individuals, 17 South Asian ancestry individuals, 3 African ancestry individuals NA Illumina [4821990] (imputed) 1 response to secukinumab, C-reactive protein measurement, arthritis disease activity score measurement http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0009435 GCST90274749 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Erythrocyte sedimentation rate x secukinumab treatment interaction in rheumatoid arthritis 193 admixed American ancestry individuals, 499 European ancestry individuals, 110 East Asian ancestry individuals, 17 South Asian ancestry individuals, 3 African ancestry individuals NA Illumina [4842993] (imputed) 0 blood sedimentation, response to secukinumab http://www.ebi.ac.uk/efo/EFO_0004304, http://www.ebi.ac.uk/efo/EFO_0022378 GCST90274750 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Health Assessment Questionnaire Disability Index x secukinumab treatment interaction in rheumatoid arthritis 193 admixed American ancestry individuals, 499 European ancestry individuals, 110 East Asian ancestry individuals, 17 South Asian ancestry individuals, 3 African ancestry individuals NA Illumina [4822706] (imputed) 0 response to secukinumab, Health Assessment Questionnaire Disability Index http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0022381 GCST90274751 Genome-wide genotyping array 2023-10-20 37659414 Zhang C 2023-08-24 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37659414 Response to anti-IL17 therapy in inflammatory disease is not strongly impacted by genetic background. Disease activity outcome x secukinumab treatment interaction in inflammatory disease 739 admixed American ancestry individuals, 4,106 European ancestry individuals, 373 East Asian ancestry, South Asian ancestry, African ancestry individuals NA Illumina [4954715] (imputed) 0 response to secukinumab, ankylosing spondylitis disease activity score, C-reactive protein measurement, arthritis disease activity score measurement, psoriasis area and severity index http://www.ebi.ac.uk/efo/EFO_0022378, http://www.ebi.ac.uk/efo/EFO_0022377, http://www.ebi.ac.uk/efo/EFO_0004458, http://www.ebi.ac.uk/efo/EFO_0009435, http://www.ebi.ac.uk/efo/EFO_0022382 GCST90274752 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine--tRNA ligase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250043 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase receptor TYRO3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tyrosine-protein kinase receptor TYRO3 measurement http://www.ebi.ac.uk/efo/EFO_0020829 GCST90250044 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase Yes levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tyrosine-protein kinase YES measurement http://www.ebi.ac.uk/efo/EFO_0020832 GCST90250045 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcriptional repressor protein YY1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250046 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase ZAP-70 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 tyrosine-protein kinase ZAP-70 measurement http://www.ebi.ac.uk/efo/EFO_0020833 GCST90250047 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tight junction protein ZO-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tight junction protein ZO-1 measurement http://www.ebi.ac.uk/efo/EFO_0803155 GCST90250048 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Splicing factor U2AF 65 kDa subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 splicing factor U2AF 65 kDa subunit measurement http://www.ebi.ac.uk/efo/EFO_0803101 GCST90250049 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uronyl 2-sulfotransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 uronyl 2-sulfotransferase measurement http://www.ebi.ac.uk/efo/EFO_0803240 GCST90250050 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. U6 snRNA-associated Sm-like protein LSm4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250051 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myoneurin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248554 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myocilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248555 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myoglobin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 myoglobin measurement http://www.ebi.ac.uk/efo/EFO_0005057 GCST90248556 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myomesin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 myomesin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802771 GCST90248557 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myomesin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248558 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myelin protein P0 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 myelin protein P0 measurement http://www.ebi.ac.uk/efo/EFO_0801813 GCST90248559 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myosin-binding protein C, slow-type levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 myosin-binding protein C, slow-type measurement http://www.ebi.ac.uk/efo/EFO_0802772 GCST90248560 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone H2A deubiquitinase MYSM1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 histone H2A deubiquitinase MYSM1 measurement http://www.ebi.ac.uk/efo/EFO_0802602 GCST90248561 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myocardial zonula adherens protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 myocardial zonula adherens protein measurement http://www.ebi.ac.uk/efo/EFO_0802769 GCST90248562 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Marginal zone B- and B1-cell-specific protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 marginal zone B- and B1-cell-specific protein measurement http://www.ebi.ac.uk/efo/EFO_0802730 GCST90248563 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Myeloid zinc finger 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 myeloid zinc finger 1 measurement http://www.ebi.ac.uk/efo/EFO_0802768 GCST90248564 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N(G),N(G)-dimethylarginine dimethylaminohydrolase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248565 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248566 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Na(+)/H(+) exchange regulatory cofactor NHE-RF3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248567 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acylneuraminate-9-phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248568 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-alpha-acetyltransferase 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248569 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-taxilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 alpha-taxilin measurement http://www.ebi.ac.uk/efo/EFO_0801375 GCST90250018 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin-like protein 4B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250019 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin domain-containing protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thioredoxin domain-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802128 GCST90250020 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 thioredoxin-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0803149 GCST90250021 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin reductase 1, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 thioredoxin reductase 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0802129 GCST90250022 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosyl-DNA phosphodiesterase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosyl-DNA phosphodiesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803210 GCST90250023 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein phosphatase non-receptor type 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90250024 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein phosphatase non-receptor type 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein phosphatase non-receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0020836 GCST90250025 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein phosphatase non-receptor type 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tyrosine-protein phosphatase non-receptor type 4 measurement http://www.ebi.ac.uk/efo/EFO_0802172 GCST90250026 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein phosphatase non-receptor type 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein phosphatase non-receptor type 7 measurement http://www.ebi.ac.uk/efo/EFO_0802173 GCST90250027 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein phosphatase non-receptor type 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein phosphatase non-receptor type 9 measurement http://www.ebi.ac.uk/efo/EFO_0802174 GCST90250028 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase ABL1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein kinase ABL1 measurement http://www.ebi.ac.uk/efo/EFO_0020818 GCST90250029 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase BTK levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein kinase BTK measurement http://www.ebi.ac.uk/efo/EFO_0020819 GCST90250030 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase CSK levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein kinase CSK measurement http://www.ebi.ac.uk/efo/EFO_0020820 GCST90250031 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase Fer levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tyrosine-protein kinase FER measurement http://www.ebi.ac.uk/efo/EFO_0020821 GCST90250032 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase Fgr levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tyrosine-protein kinase FGR measurement http://www.ebi.ac.uk/efo/EFO_0020822 GCST90250033 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase Fyn levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein kinase FYN measurement http://www.ebi.ac.uk/efo/EFO_0020823 GCST90250034 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase Lck levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90250035 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase Lyn levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tyrosine-protein kinase lyn measurement http://www.ebi.ac.uk/efo/EFO_0020827 GCST90250036 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein phosphatase non-receptor type substrate 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein phosphatase non-receptor type substrate 1 measurement http://www.ebi.ac.uk/efo/EFO_0802175 GCST90250037 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase transmembrane receptor ROR2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tyrosine-protein kinase transmembrane receptor ROR2 measurement http://www.ebi.ac.uk/efo/EFO_0803209 GCST90250038 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase RYK levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein kinase RYK measurement http://www.ebi.ac.uk/efo/EFO_0803208 GCST90250039 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase SYK levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250040 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase Tec levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tyrosine-protein kinase TEC measurement http://www.ebi.ac.uk/efo/EFO_0020830 GCST90250041 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tyrosine-protein kinase receptor Tie-1, soluble levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 tyrosine-protein kinase receptor Tie-1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008312 GCST90250042 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroligin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248690 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroligin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248691 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroligin-4, X-linked levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 neuroligin-4, x-linked measurement http://www.ebi.ac.uk/efo/EFO_0020601 GCST90248692 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuromedin-B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neuromedin-B measurement http://www.ebi.ac.uk/efo/EFO_0802803 GCST90248693 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Normal mucosa of esophagus-specific gene 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 normal mucosa of esophagus-specific gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0801846 GCST90248694 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248695 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NmrA-like family domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 nmrA-like family domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801844 GCST90248696 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuromedin-U levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248697 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-myc-interactor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248698 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuronatin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248699 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nicotinamide N-methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248700 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nodal homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248701 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Noelin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248702 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Noelin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248703 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Noelin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248704 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Noggin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 13 noggin measurement http://www.ebi.ac.uk/efo/EFO_0021995 GCST90248705 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Noncompact myelin-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 noncompact myelin-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0802818 GCST90248706 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Non-histone chromosomal protein HMG-14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 non-histone chromosomal protein HMG-14 measurement http://www.ebi.ac.uk/efo/EFO_0021872 GCST90248707 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Non-secretory ribonuclease levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 non-secretory ribonuclease measurement http://www.ebi.ac.uk/efo/EFO_0801845 GCST90248708 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Non-receptor tyrosine-protein kinase TYK2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 non-receptor tyrosine-protein kinase TYK2 measurement http://www.ebi.ac.uk/efo/EFO_0008251 GCST90248709 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurogenic locus notch homolog protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 neurogenic locus notch homolog protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008246 GCST90248710 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurogenic locus notch homolog protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90248711 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein NOV homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein nov homolog measurement http://www.ebi.ac.uk/efo/EFO_0020685 GCST90248712 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleosome assembly protein 1-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248713 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleosome assembly protein 1-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nucleosome assembly protein 1-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801857 GCST90248714 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Urotensin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250138 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Urotensin-2 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 urotensin-2 receptor measurement http://www.ebi.ac.uk/efo/EFO_0803242 GCST90250139 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uromodulin-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uromodulin-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0803239 GCST90250140 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uromodulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0021778 GCST90250141 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Urea transporter 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 urea transporter 2 measurement http://www.ebi.ac.uk/efo/EFO_0802203 GCST90250142 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-glucuronic acid decarboxylase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 UDP-glucuronic acid decarboxylase 1 measurement http://www.ebi.ac.uk/efo/EFO_0803221 GCST90250143 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Valacyclovir hydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250144 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Valine--tRNA ligase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 valine--tRNA ligase measurement http://www.ebi.ac.uk/efo/EFO_0802210 GCST90250145 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle-associated membrane protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vesicle-associated membrane protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803251 GCST90250146 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle-associated membrane protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 vesicle-associated membrane protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803252 GCST90250147 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle-associated membrane protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250148 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle-associated membrane protein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 vesicle-associated membrane protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0803254 GCST90250149 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle-associated membrane protein-associated protein B/C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vesicle-associated membrane protein-associated protein B/C measurement http://www.ebi.ac.uk/efo/EFO_0803255 GCST90250150 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vasorin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250151 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vasodilator-stimulated phosphoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250152 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vesicle-fusing ATPase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 vesicle-fusing ATPase measurement http://www.ebi.ac.uk/efo/EFO_0802214 GCST90250153 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Voltage-dependent calcium channel subunit alpha-2/delta-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 voltage-dependent calcium channel subunit alpha-2/delta-3 measurement http://www.ebi.ac.uk/efo/EFO_0802218 GCST90250154 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Voltage-dependent L-type calcium channel subunit beta-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250155 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular cell adhesion protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 vascular cell adhesion protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020846 GCST90250156 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Versican core protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 versican core protein measurement http://www.ebi.ac.uk/efo/EFO_0803248 GCST90250157 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular endothelial growth factor A, isoform 121 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 vascular endothelial growth factor A, isoform 121 measurement http://www.ebi.ac.uk/efo/EFO_0020847 GCST90250158 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular endothelial growth factor A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90250159 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular endothelial growth factor B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250160 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular endothelial growth factor C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 vascular endothelial growth factor C measurement http://www.ebi.ac.uk/efo/EFO_0020848 GCST90250161 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. vascular endothelial growth factor D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90250162 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular endothelial growth factor receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250163 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular endothelial growth factor receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90250164 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vascular endothelial growth factor receptor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90250165 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vigilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vigilin measurement http://www.ebi.ac.uk/efo/EFO_0802215 GCST90250166 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. V-type immunoglobulin domain-containing suppressor of T-cell activation levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 10 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250167 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vimentin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250168 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vinexin b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vinexin b measurement http://www.ebi.ac.uk/efo/EFO_0803258 GCST90250169 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vasoactive Intestinal Peptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 vasoactive intestinal peptide measurement http://www.ebi.ac.uk/efo/EFO_0020849 GCST90250170 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. VIP36-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 VIP36-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802216 GCST90250171 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vitamin D-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST90250172 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vitamin D3 receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250173 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vitamin K-dependent protein C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90250174 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vitamin K-dependent protein S levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 vitamin k-dependent protein S measurement http://www.ebi.ac.uk/efo/EFO_0020850 GCST90250175 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vitrin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 vitrin measurement http://www.ebi.ac.uk/efo/EFO_0802217 GCST90250176 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Vitronectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90250177 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Voltage-gated potassium channel subunit beta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 voltage-gated potassium channel subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0802219 GCST90250178 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear inhibitor of protein phosphatase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248681 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nischarin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 nischarin measurement http://www.ebi.ac.uk/efo/EFO_0801841 GCST90248682 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Omega-amidase NIT2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248683 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Natural killer cell receptor 2B4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 natural killer cell receptor 2B4 measurement http://www.ebi.ac.uk/efo/EFO_0021882 GCST90248684 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NKG2-D type II integral membrane protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 NKG2-D type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0008250 GCST90248685 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NKG2D ligand 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 NKG2D ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0802815 GCST90248686 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NKG2D ligand 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 NKG2D ligand 3 measurement http://www.ebi.ac.uk/efo/EFO_0802816 GCST90248687 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NKG2-E type II integral membrane protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 NKG2-E type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801842 GCST90248688 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroligin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neuroligin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802802 GCST90248689 Genome-wide genotyping array 2023-03-14 34233476 Leon-Mimila P 2021-07-08 Arterioscler Thromb Vasc Biol www.ncbi.nlm.nih.gov/pubmed/34233476 Genome-Wide Association Study Identifies a Functional SIDT2 Variant Associated With HDL-C (High-Density Lipoprotein Cholesterol) Levels and Premature Coronary Artery Disease. HDL cholesterol levels 2,335 Mexican ancestry individuals 2,114 Mexican ancestry individuals, 302 Totonac and Nahua ancestry individuals Illumina [624242] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90027265 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Actin-related protein 2/3 complex subunit 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 actin-related protein 2/3 complex subunit 3 measurement http://www.ebi.ac.uk/efo/EFO_0802252 GCST90248816 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha- and gamma-adaptin-binding protein p34 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248817 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0801881 GCST90248818 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolyl 3-hydroxylase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248819 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylinositol 3-kinase regulatory subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248820 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome P450 3A4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 cytochrome p450 3a4 measurement http://www.ebi.ac.uk/efo/EFO_0020303 GCST90248821 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pterin-4-alpha-carbinolamine dehydratase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248822 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pterin-4-alpha-carbinolamine dehydratase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248823 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolyl 4-hydroxylase subunit alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 prolyl 4-hydroxylase subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0802917 GCST90248824 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prolyl 4-hydroxylase subunit alpha-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 prolyl 4-hydroxylase subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0802918 GCST90248825 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cellular tumor antigen p53 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cellular tumor antigen p53 measurement http://www.ebi.ac.uk/efo/EFO_0022006 GCST90248826 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. p53 and DNA damage-regulated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 p53 and DNA damage-regulated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803313 GCST90248827 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cellular tumor antigen p53 R175H mutant levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248828 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyrroline-5-carboxylate reductase 1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248829 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyrroline-5-carboxylate reductase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248830 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyridoxine-5-phosphate oxidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248831 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phospholipase A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248832 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Proliferation-associated protein 2G4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 proliferation-associated protein 2g4 measurement http://www.ebi.ac.uk/efo/EFO_0020658 GCST90248833 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phospholipase A2, membrane associated levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90248834 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pancreatic alpha-amylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248835 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polyadenylate-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248836 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polyadenylate-binding protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 polyadenylate-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0801896 GCST90248837 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Polyadenylate-binding protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 polyadenylate-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801897 GCST90248838 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pituitary adenylate cyclase-activating polypeptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pituitary adenylate cyclase-activating polypeptide measurement http://www.ebi.ac.uk/efo/EFO_0802869 GCST90248839 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pituitary adenylate cyclase-activating polypeptide 27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pituitary adenylate cyclase-activating polypeptide 27 measurement http://www.ebi.ac.uk/efo/EFO_0020640 GCST90248840 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pituitary adenylate cyclase-activating polypeptide 38 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pituitary adenylate cyclase-activating polypeptide 38 measurement http://www.ebi.ac.uk/efo/EFO_0020641 GCST90248841 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PCNA-associated factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248842 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-activating factor acetylhydrolase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248843 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Platelet-activating factor acetylhydrolase 2, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248844 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein argonaute-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein argonaute-1 measurement http://www.ebi.ac.uk/efo/EFO_0802926 GCST90248845 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pancreatic lipase-related protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248850 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pancreatic triacylglycerol lipase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248851 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostatic acid phosphatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248852 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pappalysin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 pappalysin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802845 GCST90248853 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pappalysin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 pappalysin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802846 GCST90248854 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Paralemmin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248855 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mono [ADP-ribose] polymerase PARP16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248856 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-parvin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 alpha-parvin measurement http://www.ebi.ac.uk/efo/EFO_0802271 GCST90248857 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostate and testis expressed protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 prostate and testis expressed protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802919 GCST90248858 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Prostate and testis expressed protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 prostate and testis expressed protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803301 GCST90248859 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PRKC apoptosis WT1 regulator protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248860 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Paired box protein Pax-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 paired box protein Pax-4 measurement http://www.ebi.ac.uk/efo/EFO_0802841 GCST90248861 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PAX-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 PAX-interacting protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801868 GCST90248862 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein polybromo-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248863 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphatidylethanolamine-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 phosphatidylethanolamine-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020634 GCST90248864 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable RNA-binding protein 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 probable RNA-binding protein 19 measurement http://www.ebi.ac.uk/efo/EFO_0802909 GCST90248865 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable RNA-binding protein 23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 probable RNA-binding protein 23 measurement http://www.ebi.ac.uk/efo/EFO_0801917 GCST90248866 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable RNA-binding protein 46 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248867 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. PC4 and SFRS1-interacting protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248868 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Putative chondrosarcoma-associated gene 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 putative chondrosarcoma-associated gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802980 GCST90248869 Genome-wide genotyping array 2023-05-31 37090135 Sakashita T 2023-01-27 Diabetol Int www.ncbi.nlm.nih.gov/pubmed/37090135 Comparison of the loci associated with HbA1c and blood glucose levels identified by a genome-wide association study in the Japanese population. Glycated hemoglobin HbA1c levels 4,911 Japanese ancestry individuals 48,694 Japanese ancestry individuals Illumina [8280776] (imputed) 4 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90270078 Genome-wide genotyping array 2023-05-31 37090135 Sakashita T 2023-01-27 Diabetol Int www.ncbi.nlm.nih.gov/pubmed/37090135 Comparison of the loci associated with HbA1c and blood glucose levels identified by a genome-wide association study in the Japanese population. Fasting glucose 4,911 Japanese ancestry individuals 48,694 Japanese ancestry individuals Illumina [8280776] (imputed) 0 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90270079 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcobalamin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249968 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Triggering receptor expressed on myeloid cells 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 triggering receptor expressed on myeloid cells 1 measurement http://www.ebi.ac.uk/efo/EFO_0802161 GCST90249969 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Triggering receptor expressed on myeloid cells 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249970 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Three prime repair exonuclease 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249971 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transforming protein RhoA levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transforming protein RhoA measurement http://www.ebi.ac.uk/efo/EFO_0802144 GCST90249972 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tripartite motif-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249973 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trem-like transcript 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 trem-like transcript 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0803193 GCST90249974 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trem-like transcript 2 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 trem-like transcript 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0802159 GCST90249975 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. tRNA (cytosine(38)-C(5))-methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249976 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. tRNA-dihydrouridine(20) synthase [NAD(P)+]-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249977 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. tRNA (guanine-N(7)-)-methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 tRNA (guanine-N(7)-)-methyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0802162 GCST90249978 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transferrin receptor protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 transferrin receptor protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802142 GCST90249979 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transferrin receptor protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249980 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tudor-interacting repair regulator protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249981 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trypsin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 trypsin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020790 GCST90249982 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trypsin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 trypsin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008305 GCST90249983 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Trypsin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 trypsin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020791 GCST90249984 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tryptase beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249985 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thymidylate synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 thymidylate synthase measurement http://www.ebi.ac.uk/efo/EFO_0020774 GCST90249986 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Testis-specific chromodomain protein Y 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 testis-specific chromodomain protein Y 1 measurement http://www.ebi.ac.uk/efo/EFO_0802127 GCST90249987 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombospondin-type laminin G domain and EAR repeat-containing protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249988 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor necrosis factor-inducible gene 6 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tumor necrosis factor-inducible gene 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0008311 GCST90249989 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thyroid stimulating hormone levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST90249990 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tensin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tensin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802122 GCST90249991 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tensin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tensin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802123 GCST90249992 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Translin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 translin measurement http://www.ebi.ac.uk/efo/EFO_0803172 GCST90249993 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. t-SNARE domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 t-SNARE domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802116 GCST90249994 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombospondin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90249995 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombospondin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thrombospondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0803151 GCST90249996 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thrombospondin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thrombospondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020771 GCST90249997 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein TSSC4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249998 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tetratricopeptide repeat protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249999 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tetratricopeptide repeat protein 17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tetratricopeptide repeat protein 17 measurement http://www.ebi.ac.uk/efo/EFO_0803144 GCST90250000 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tetratricopeptide repeat protein 9B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tetratricopeptide repeat protein 9B measurement http://www.ebi.ac.uk/efo/EFO_0803145 GCST90250001 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Type III endosome membrane protein TEMP levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 type III endosome membrane protein TEMP measurement http://www.ebi.ac.uk/efo/EFO_0803207 GCST90250002 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tubulin--tyrosine ligase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tubulin--tyrosine ligase measurement http://www.ebi.ac.uk/efo/EFO_0802165 GCST90250003 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Threonine--tRNA ligase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250004 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor susceptibility gene 101 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor susceptibility gene 101 protein measurement http://www.ebi.ac.uk/efo/EFO_0803203 GCST90250005 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor-associated calcium signal transducer 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tumor-associated calcium signal transducer 2 measurement http://www.ebi.ac.uk/efo/EFO_0020817 GCST90250006 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor protein 63 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 tumor protein 63 measurement http://www.ebi.ac.uk/efo/EFO_0803202 GCST90250007 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor protein D53 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250008 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor protein p53-inducible protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 tumor protein p53-inducible protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0802169 GCST90250009 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tumor protein p53-inducible protein 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250010 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Twisted gastrulation protein homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 twisted gastrulation protein homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0803205 GCST90250011 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 thioredoxin measurement http://www.ebi.ac.uk/efo/EFO_0803148 GCST90250012 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tax1-binding protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 tax1-binding protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802120 GCST90250013 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin domain-containing protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thioredoxin domain-containing protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0803147 GCST90250014 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin domain-containing protein 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90250015 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin domain-containing protein 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250016 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thioredoxin-dependent peroxide reductase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250017 Genome-wide genotyping array 2023-04-05 36525587 Campos AI 2022-12-16 Sleep www.ncbi.nlm.nih.gov/pubmed/36525587 Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep apnea syndrome 25,008 European ancestry cases, 337,630 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 3 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90267361 Genome-wide genotyping array 2023-04-05 36525587 Campos AI 2022-12-16 Sleep www.ncbi.nlm.nih.gov/pubmed/36525587 Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep apnea (MTAG) 159,255 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 21 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90267362 Genome-wide genotyping array 2023-04-05 36525587 Campos AI 2022-12-16 Sleep www.ncbi.nlm.nih.gov/pubmed/36525587 Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep apnea (adjusted for BMI) 25,008 European ancestry cases, 337,630 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 1 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90267363 Genome-wide genotyping array 2023-04-05 36525587 Campos AI 2022-12-16 Sleep www.ncbi.nlm.nih.gov/pubmed/36525587 Discovery of genomic loci associated with sleep apnoea risk through multi-trait GWAS analysis with snoring. Sleep apnea (MTAG) (adjusted for BMI) 159,255 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 5 sleep apnea http://www.ebi.ac.uk/efo/EFO_0003877 GCST90267364 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transcriptional regulator Kaiso levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 transcriptional regulator Kaiso measurement http://www.ebi.ac.uk/efo/EFO_0803168 GCST90249886 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thymidine kinase, cytosolic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 thymidine kinase, cytosolic measurement http://www.ebi.ac.uk/efo/EFO_0020773 GCST90249887 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thymidine kinase 2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249888 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tachykinin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 tachykinin-4 measurement http://www.ebi.ac.uk/efo/EFO_0803137 GCST90249889 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Tolloid-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 tolloid-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802135 GCST90249890 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Talin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 talin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802117 GCST90249891 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Toll-like receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 toll-like receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0803159 GCST90249892 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Toll-like receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 toll-like receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020777 GCST90249893 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Toll-like receptor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249894 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. TLR4 interactor with leucine rich repeats levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249895 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Toll-like receptor 4:Lymphocyte antigen 96 complex levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90249896 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Toll-like receptor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249897 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. T-lymphocyte surface antigen Ly-9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 T-lymphocyte surface antigen Ly-9 measurement http://www.ebi.ac.uk/efo/EFO_0008295 GCST90249898 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 119 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane protein 119 measurement http://www.ebi.ac.uk/efo/EFO_0803182 GCST90249899 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protease serine 11B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane protease serine 11B measurement http://www.ebi.ac.uk/efo/EFO_0803180 GCST90249900 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protease serine 11D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 transmembrane protease serine 11D measurement http://www.ebi.ac.uk/efo/EFO_0802149 GCST90249901 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 132A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 transmembrane protein 132A measurement http://www.ebi.ac.uk/efo/EFO_0802150 GCST90249902 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 132B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 transmembrane protein 132B measurement http://www.ebi.ac.uk/efo/EFO_0802151 GCST90249903 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 132C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 transmembrane protein 132C measurement http://www.ebi.ac.uk/efo/EFO_0802152 GCST90249904 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 132D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane protein 132D measurement http://www.ebi.ac.uk/efo/EFO_0802153 GCST90249905 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 154 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249906 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 185A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249907 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 190 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane protein 190 measurement http://www.ebi.ac.uk/efo/EFO_0802154 GCST90249908 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 transmembrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802155 GCST90249909 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 230 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane protein 230 measurement http://www.ebi.ac.uk/efo/EFO_0802156 GCST90249910 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 52 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 transmembrane protein 52 measurement http://www.ebi.ac.uk/efo/EFO_0803187 GCST90249911 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 52B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249912 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 59-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 transmembrane protein 59-like measurement http://www.ebi.ac.uk/efo/EFO_0802157 GCST90249913 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 87B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 transmembrane protein 87B measurement http://www.ebi.ac.uk/efo/EFO_0802158 GCST90249914 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 transmembrane protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0803190 GCST90249915 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Thyroid peroxidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 thyroid peroxidase measurement http://www.ebi.ac.uk/efo/EFO_0020775 GCST90249916 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein C16orf54 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane protein C16orf54 measurement http://www.ebi.ac.uk/efo/EFO_0803191 GCST90249917 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protein C1orf162 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249918 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane and coiled-coil domain-containing protein 5A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane and coiled-coil domain-containing protein 5A measurement http://www.ebi.ac.uk/efo/EFO_0803174 GCST90249919 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane and coiled-coil domains protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90249920 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane emp24 domain-containing protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane emp24 domain-containing protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0802146 GCST90249921 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane emp24 domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane emp24 domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803177 GCST90249922 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane gamma-carboxyglutamic acid protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 transmembrane gamma-carboxyglutamic acid protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802147 GCST90249923 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Transmembrane protease serine 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 transmembrane protease serine 5 measurement http://www.ebi.ac.uk/efo/EFO_0803181 GCST90249924 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. U6 snRNA phosphodiesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 U6 snRNA phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0803211 GCST90250052 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-like-conjugating enzyme ATG3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250053 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 D1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250054 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 D2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250055 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 D3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250056 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 D4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquitin-conjugating enzyme E2 D4 measurement http://www.ebi.ac.uk/efo/EFO_0802181 GCST90250057 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 E1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250058 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 G1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250059 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 G2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ubiquitin-conjugating enzyme E2 G2 measurement http://www.ebi.ac.uk/efo/EFO_0022035 GCST90250060 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 J1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquitin-conjugating enzyme E2 J1 measurement http://www.ebi.ac.uk/efo/EFO_0803215 GCST90250061 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 L3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquitin-conjugating enzyme E2 L3 measurement http://www.ebi.ac.uk/efo/EFO_0020840 GCST90250062 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fas apoptotic inhibitory molecule 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 fas apoptotic inhibitory molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0802540 GCST90247550 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fatty acid-binding protein, intestinal levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247551 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Focal adhesion kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 focal adhesion kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020393 GCST90247552 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fatty acid-binding protein, liver levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fatty acid-binding protein, liver measurement http://www.ebi.ac.uk/efo/EFO_0021855 GCST90247553 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fanconi anemia group F protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247554 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fatty acid synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247555 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fructose-bisphosphate aldolase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fructose-bisphosphate aldolase A measurement http://www.ebi.ac.uk/efo/EFO_0801608 GCST90247556 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fructose-bisphosphate aldolase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247557 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fructose-bisphosphate aldolase C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fructose-bisphosphate aldolase C measurement http://www.ebi.ac.uk/efo/EFO_0802557 GCST90247558 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. F-box only protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 f-box only protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802537 GCST90247559 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. F-box/LRR-repeat protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 f-box/LRR-repeat protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802538 GCST90247560 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low affinity immunoglobulin gamma Fc region receptor II-a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 low affinity immunoglobulin gamma Fc region receptor II-a measurement http://www.ebi.ac.uk/efo/EFO_0021969 GCST90247561 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low affinity immunoglobulin gamma Fc region receptor II-b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 low affinity immunoglobulin gamma Fc region receptor II-b measurement http://www.ebi.ac.uk/efo/EFO_0021970 GCST90247562 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low affinity immunoglobulin gamma Fc region receptor III-A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247563 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Low affinity immunoglobulin gamma Fc region receptor III-B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 low affinity immunoglobulin gamma Fc region receptor III-B measurement http://www.ebi.ac.uk/efo/EFO_0008212 GCST90247564 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fc receptor-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 Fc receptor-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801598 GCST90247565 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fc receptor-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 Fc receptor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008127 GCST90247566 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fc receptor-like protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 Fc receptor-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801599 GCST90247567 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fc receptor-like protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 Fc receptor-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802545 GCST90247568 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fc receptor-like protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 Fc receptor-like protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0801600 GCST90247569 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fc receptor-like B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247570 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Follicular dendritic cell secreted peptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247571 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Flap endonuclease 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 flap endonuclease 1 measurement http://www.ebi.ac.uk/efo/EFO_0802551 GCST90247572 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ferritin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90247573 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Iron-sulfur cluster co-chaperone protein HscB, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247574 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fetuin-B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 fetuin-B measurement http://www.ebi.ac.uk/efo/EFO_0008128 GCST90247575 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FEV levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247576 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fibroblast growth factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020376 GCST90247577 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 12 measurement http://www.ebi.ac.uk/efo/EFO_0020377 GCST90247578 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90247579 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 17 measurement http://www.ebi.ac.uk/efo/EFO_0020379 GCST90247580 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 18 measurement http://www.ebi.ac.uk/efo/EFO_0020380 GCST90247581 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90247582 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fibroblast growth factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008129 GCST90247583 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 20 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 20 measurement http://www.ebi.ac.uk/efo/EFO_0020381 GCST90247584 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 22 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247585 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247586 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020382 GCST90247587 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90247588 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020383 GCST90247589 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90247590 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247591 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 8 isoform B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fibroblast growth factor 8 isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020386 GCST90247592 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 8 isoform F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247593 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020387 GCST90247594 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247595 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor-binding protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247596 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 fibroblast growth factor receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020388 GCST90247597 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor receptor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fibroblast growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020389 GCST90247598 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fibroblast growth factor receptor 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90247599 Genome-wide genotyping array 2023-06-27 37255673 Zaidi AA 2023-05-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/37255673 The genetic and phenotypic correlates of mtDNA copy number in a multi-ancestry cohort. Estimated mitochondrial DNA copy number 21,994 European ancestry individuals NA Illumina [8472317] (imputed) 2 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90267372 Genome-wide genotyping array 2023-06-27 37255673 Zaidi AA 2023-05-09 HGG Adv www.ncbi.nlm.nih.gov/pubmed/37255673 The genetic and phenotypic correlates of mtDNA copy number in a multi-ancestry cohort. Estimated mitochondrial DNA copy number 8,568 African American or Afro-Caribbean individuals NA Illumina [15312155] (imputed) 0 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90267373 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetyltransferase 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 n-acetyltransferase 14 measurement http://www.ebi.ac.uk/efo/EFO_0801819 GCST90248570 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NGFI-A-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 NGFI-A-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802811 GCST90248571 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nascent polypeptide-associated complex subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nascent polypeptide-associated complex subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020587 GCST90248572 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NACHT, LRR and PYD domains-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 NACHT, LRR and PYD domains-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802780 GCST90248573 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NAD(P)H-hydrate epimerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248574 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NAD(P)H dehydrogenase [quinone] 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248575 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nicotinate-nucleotide pyrophosphorylase [carboxylating] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248576 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetyl-D-glucosamine kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 N-acetyl-D-glucosamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0008239 GCST90248577 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248578 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248579 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248580 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NAD kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 NAD kinase measurement http://www.ebi.ac.uk/efo/EFO_0801821 GCST90248581 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alcohol dehydrogenase [NADP(+)] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248582 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NADPH--cytochrome P450 reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 NADPH--cytochrome P450 reductase measurement http://www.ebi.ac.uk/efo/EFO_0008242 GCST90248583 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NAD-dependent protein deacetylase sirtuin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 NAD-dependent protein deacetylase sirtuin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008241 GCST90248584 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NAD-dependent protein deacetylase sirtuin-3, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248585 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NAD-dependent protein deacylase sirtuin-5, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 NAD-dependent protein deacylase sirtuin-5, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801822 GCST90248586 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Alpha-N-acetylglucosaminidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248587 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 n-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase measurement http://www.ebi.ac.uk/efo/EFO_0801816 GCST90248588 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylglucosamine-1-phosphotransferase subunit gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 n-acetylglucosamine-1-phosphotransferase subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0802775 GCST90248589 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylglucosamine-6-sulfatase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90248590 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylglutamate synthase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 n-acetylglutamate synthase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802776 GCST90248591 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acylethanolamine-hydrolyzing acid amidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90248592 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear apoptosis-inducing factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248593 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylmuramoyl-L-alanine amidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248594 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuropilin and tolloid-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neuropilin and tolloid-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802807 GCST90248645 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuregulin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neuregulin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022029 GCST90248646 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuregulin-1, sensory and motor neuron-derived factor isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248647 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuregulin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neuregulin-4 measurement http://www.ebi.ac.uk/efo/EFO_0021951 GCST90248648 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear nucleic acid-binding protein C1D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 nuclear nucleic acid-binding protein C1D measurement http://www.ebi.ac.uk/efo/EFO_0802820 GCST90248649 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutral ceramidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90248650 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil collagenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 neutrophil collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008248 GCST90248651 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil defensin 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248652 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil elastase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 neutrophil elastase measurement http://www.ebi.ac.uk/efo/EFO_0020605 GCST90248653 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuferricin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248654 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurogranin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248655 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil gelatinase-associated lipocalin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 neutrophil gelatinase-associated lipocalin measurement http://www.ebi.ac.uk/efo/EFO_0021964 GCST90248656 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase NEURL1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 E3 ubiquitin-protein ligase NEURL1 measurement http://www.ebi.ac.uk/efo/EFO_0801554 GCST90248657 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuralized-like protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neuralized-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802796 GCST90248658 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuromodulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248659 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear protein MDM1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 nuclear protein MDM1 measurement http://www.ebi.ac.uk/efo/EFO_0802822 GCST90248660 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear migration protein nudC levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear migration protein nudC measurement http://www.ebi.ac.uk/efo/EFO_0801849 GCST90248661 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuropeptide S levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neuropeptide S measurement http://www.ebi.ac.uk/efo/EFO_0802806 GCST90248662 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuropeptide W levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neuropeptide W measurement http://www.ebi.ac.uk/efo/EFO_0801835 GCST90248663 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear receptor ROR-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear receptor ROR-beta measurement http://www.ebi.ac.uk/efo/EFO_0802823 GCST90248664 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear factor erythroid 2-related factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nuclear factor erythroid 2-related factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801848 GCST90248665 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurofascin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 neurofascin measurement http://www.ebi.ac.uk/efo/EFO_0801831 GCST90248666 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear factor of activated T-cells, cytoplasmic 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248667 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurofilament heavy polypeptide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neurofilament heavy polypeptide measurement http://www.ebi.ac.uk/efo/EFO_0802801 GCST90248668 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NF-kappa-B inhibitor beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248669 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylated-alpha-linked acidic dipeptidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 n-acetylated-alpha-linked acidic dipeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801815 GCST90248595 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylated-alpha-linked acidic dipeptidase-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248596 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylneuraminate lyase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248597 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homeobox protein NANOG levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 homeobox protein nanog measurement http://www.ebi.ac.uk/efo/EFO_0020456 GCST90248598 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetylserotonin O-methyltransferase-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 n-acetylserotonin O-methyltransferase-like protein measurement http://www.ebi.ac.uk/efo/EFO_0801818 GCST90248599 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil-activating peptide 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neutrophil-activating peptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020606 GCST90248600 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. nucleosome assembly protein 1-like 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248601 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein NATD1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248602 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 n-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801817 GCST90248603 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248604 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NADH-cytochrome b5 reductase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248605 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NADH-cytochrome b5 reductase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248606 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. N-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase, isoform C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 n-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase, isoform C measurement http://www.ebi.ac.uk/efo/EFO_0802777 GCST90248607 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Next to BRCA1 gene 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 next to BRCA1 gene 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0801838 GCST90248608 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurocalcin-delta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248609 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuron-specific vesicular protein calcyon levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 neuron-specific vesicular protein calcyon measurement http://www.ebi.ac.uk/efo/EFO_0802805 GCST90248610 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neural cell adhesion molecule 1, 120 kDa isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 neural cell adhesion molecule 1, 120 kda isoform measurement http://www.ebi.ac.uk/efo/EFO_0020593 GCST90248611 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neural cell adhesion molecule 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 neural cell adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0801827 GCST90248612 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neural cell adhesion molecule L1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neural cell adhesion molecule L1 measurement http://www.ebi.ac.uk/efo/EFO_0020594 GCST90248613 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil cytosol factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248614 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil cytosol factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 neutrophil cytosol factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0801837 GCST90248615 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neutrophil cytosol factor 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248616 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neural cell adhesion molecule L1-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 neural cell adhesion molecule l1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020595 GCST90248617 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear receptor coactivator 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 nuclear receptor coactivator 2 measurement http://www.ebi.ac.uk/efo/EFO_0801852 GCST90248618 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neurocan core protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248619 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Kinetochore protein NDC80 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 kinetochore protein NDC80 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801748 GCST90248620 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nuclear distribution protein nudE homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248621 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleoside diphosphate kinase A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nucleoside diphosphate kinase A measurement http://www.ebi.ac.uk/efo/EFO_0009947 GCST90248622 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleoside diphosphate kinase B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 nucleoside diphosphate kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020615 GCST90248623 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nucleoside diphosphate kinase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248624 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein NDRG1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248625 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein NDRG3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248626 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein NDRG4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein NDRG4 measurement http://www.ebi.ac.uk/efo/EFO_0801954 GCST90248627 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802332 GCST90248628 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroendocrine convertase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 neuroendocrine convertase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801830 GCST90248629 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroendocrine convertase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248630 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nectin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802789 GCST90248631 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nectin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 nectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0802788 GCST90248632 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NEDD8-activating enzyme E1 regulatory subunit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248633 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NEDD8-conjugating enzyme Ubc12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248634 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. NEDD8-conjugating enzyme UBE2F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248635 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuronal growth regulator 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 neuronal growth regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0021932 GCST90248636 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C-binding protein NELL1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein kinase C-binding protein NELL1 measurement http://www.ebi.ac.uk/efo/EFO_0801950 GCST90248637 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein kinase C-binding protein NELL2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein kinase C-binding protein NELL2 measurement http://www.ebi.ac.uk/efo/EFO_0802949 GCST90248638 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neogenin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 neogenin measurement http://www.ebi.ac.uk/efo/EFO_0801823 GCST90248639 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Neuroendocrine protein 7B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248640 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nephronectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248641 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Nesprin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 nesprin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801824 GCST90248642 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Netrin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 netrin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022009 GCST90248643 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Netrin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 netrin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020592 GCST90248644 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uridine-cytidine kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uridine-cytidine kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0803238 GCST90250088 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Unique cartilage matrix-associated protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 unique cartilage matrix-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0802198 GCST90250089 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-like protein ISG15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ubiquitin-like protein ISG15 measurement http://www.ebi.ac.uk/efo/EFO_0021875 GCST90250090 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized family 31 glucosidase KIAA1161 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized family 31 glucosidase KIAA1161 measurement http://www.ebi.ac.uk/efo/EFO_0802188 GCST90250091 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-fold modifier-conjugating enzyme 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ubiquitin-fold modifier-conjugating enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020843 GCST90250092 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-fold modifier 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ubiquitin-fold modifier 1 measurement http://www.ebi.ac.uk/efo/EFO_0020842 GCST90250093 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-glucose 4-epimerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250094 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-glucose 6-dehydrogenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250095 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-glucuronosyltransferase 1-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250096 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-glucuronosyltransferase 1-6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 UDP-glucuronosyltransferase 1-6 measurement http://www.ebi.ac.uk/efo/EFO_0802185 GCST90250097 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-glucuronosyltransferase 1-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 UDP-glucuronosyltransferase 1-8 measurement http://www.ebi.ac.uk/efo/EFO_0803222 GCST90250098 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-glucuronosyltransferase 2A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 UDP-glucuronosyltransferase 2A1 measurement http://www.ebi.ac.uk/efo/EFO_0802186 GCST90250099 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UPF0258 protein KIAA1024 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 UPF0258 protein KIAA1024 measurement http://www.ebi.ac.uk/efo/EFO_0803234 GCST90250100 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UPF0577 protein KIAA1324 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 UPF0577 protein KIAA1324 measurement http://www.ebi.ac.uk/efo/EFO_0803235 GCST90250101 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UPF0577 protein KIAA1324-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 UPF0577 protein KIAA1324-like measurement http://www.ebi.ac.uk/efo/EFO_0802201 GCST90250102 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UPF0606 protein KIAA1549L levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250103 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UPF0160 protein MYG1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250104 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Unconventional myosin-VI levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 unconventional myosin-VI measurement http://www.ebi.ac.uk/efo/EFO_0803233 GCST90250105 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein unc-13 homolog A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein unc-13 homolog A measurement http://www.ebi.ac.uk/efo/EFO_0802968 GCST90250106 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein unc-45 homolog A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250107 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UDP-N-acetylhexosamine pyrophosphorylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 UDP-N-acetylhexosamine pyrophosphorylase measurement http://www.ebi.ac.uk/efo/EFO_0802187 GCST90250108 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uroporphyrinogen-III synthase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 uroporphyrinogen-III synthase measurement http://www.ebi.ac.uk/efo/EFO_0802205 GCST90250109 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Urokinase-type plasminogen activator levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90250110 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Urokinase plasminogen activator surface receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90250111 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C10orf105 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250112 Genome-wide genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Insulin fold change during an oral glucose tolerance test (adjusted for BMI) 53,287 European ancestry individuals NA Affymetrix, Illumina [9558607] (imputed) 5 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267567 Genome-wide genotyping array, Targeted genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Insulin fold change during an oral glucose tolerance test 53,334 European ancestry individuals NA Affymetrix, Illumina [9558719] (imputed) 5 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267568 Genome-wide genotyping array, Targeted genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Insulin fold change during an oral glucose tolerance test (adjusted for BMI) 739 East Asian ancestry individuals, 1,098 Hispanic American individuals NA Illumina [10429466] (imputed) 1 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267569 Genome-wide genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Insulin fold change during an oral glucose tolerance test 739 East Asian ancestry individuals, 1,099 Hispanic American individuals NA Illumina [10429597] (imputed) 1 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267570 Genome-wide genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Insulin fold change during an oral glucose tolerance test (adjusted for BMI) 739 East Asian ancestry individuals, 1,098 Hispanic American individuals, 53,287 European ancestry individuals NA Affymetrix, Illumina [9586245] (imputed) 4 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267571 Genome-wide genotyping array, Targeted genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Insulin fold change during an oral glucose tolerance test 739 East Asian ancestry individuals, 1,099 Hispanic American individuals, 53,334 European ancestry individuals NA Affymetrix, Illumina [9588070] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267572 Genome-wide genotyping array, Targeted genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Modified Stumvoll Insulin Sensitivity Index (adjusted for BMI) 53,657 European ancestry individuals NA Affymetrix, Illumina [9743948] (imputed) 8 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267573 Genome-wide genotyping array, Targeted genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Modified Stumvoll Insulin Sensitivity Index 53,710 European ancestry individuals NA Affymetrix, Illumina [9547465] (imputed) 5 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267574 Genome-wide genotyping array, Targeted genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Modified Stumvoll Insulin Sensitivity Index (adjusted for BMI) 730 East Asian ancestry individuals, 1,094 Hispanic American individuals NA Illumina [10425738] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267575 Genome-wide genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Modified Stumvoll Insulin Sensitivity Index 730 East Asian ancestry individuals, 1,095 Hispanic American individuals NA Illumina [10425883] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267576 Genome-wide genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Modified Stumvoll Insulin Sensitivity Index (adjusted for BMI) 730 East Asian ancestry individuals, 1,094 Hispanic American individuals, 53,657 European ancestry individuals NA Affymetrix, Illumina [9768722] (imputed) 4 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267577 Genome-wide genotyping array, Targeted genotyping array 2023-06-26 37291194 Williamson A 2023-06-08 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37291194 Genome-wide association study and functional characterization identifies candidate genes for insulin-stimulated glucose uptake. Modified Stumvoll Insulin Sensitivity Index 730 East Asian ancestry individuals, 1,095 Hispanic American individuals, 53,710 European ancestry individuals NA Affymetrix, Illumina [9769301] (imputed) 0 insulin resistance http://www.ebi.ac.uk/efo/EFO_0002614 GCST90267578 Genome-wide genotyping array, Targeted genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C10orf35 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 uncharacterized protein C10orf35 measurement http://www.ebi.ac.uk/efo/EFO_0802189 GCST90250113 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C11orf87 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250114 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C11orf94 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250115 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C14orf93 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 uncharacterized protein C14orf93 measurement http://www.ebi.ac.uk/efo/EFO_0802190 GCST90250116 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C17orf67 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C17orf67 measurement http://www.ebi.ac.uk/efo/EFO_0803223 GCST90250117 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C17orf78 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C17orf78 measurement http://www.ebi.ac.uk/efo/EFO_0802191 GCST90250118 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C17orf89 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C17orf89 measurement http://www.ebi.ac.uk/efo/EFO_0803224 GCST90250119 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C19orf18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 uncharacterized protein C19orf18 measurement http://www.ebi.ac.uk/efo/EFO_0803225 GCST90250120 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C1orf115 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C1orf115 measurement http://www.ebi.ac.uk/efo/EFO_0803226 GCST90250121 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C1orf185 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C1orf185 measurement http://www.ebi.ac.uk/efo/EFO_0803227 GCST90250122 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C1orf198 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C1orf198 measurement http://www.ebi.ac.uk/efo/EFO_0803228 GCST90250123 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C20orf173 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250124 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C22orf15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C22orf15 measurement http://www.ebi.ac.uk/efo/EFO_0803230 GCST90250125 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C2orf66 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 uncharacterized protein C2orf66 measurement http://www.ebi.ac.uk/efo/EFO_0802192 GCST90250126 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C3orf18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 uncharacterized protein C3orf18 measurement http://www.ebi.ac.uk/efo/EFO_0802193 GCST90250127 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C4orf32 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250128 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C5orf46 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250129 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C7orf69 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 uncharacterized protein C7orf69 measurement http://www.ebi.ac.uk/efo/EFO_0802195 GCST90250130 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein C7orf73 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250131 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uroporphyrinogen decarboxylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250132 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein KIAA0040 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 uncharacterized protein KIAA0040 measurement http://www.ebi.ac.uk/efo/EFO_0802196 GCST90250133 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein KIAA1644 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250134 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uncharacterized protein KIAA2013 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 uncharacterized protein KIAA2013 measurement http://www.ebi.ac.uk/efo/EFO_0802197 GCST90250135 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uroplakin-3b-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 uroplakin-3b-like protein measurement http://www.ebi.ac.uk/efo/EFO_0802204 GCST90250136 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Uridine phosphorylase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250137 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 variant 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquitin-conjugating enzyme E2 variant 1 measurement http://www.ebi.ac.uk/efo/EFO_0802182 GCST90250063 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 variant 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250064 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-like domain-containing CTD phosphatase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250065 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250066 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250067 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250068 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 N levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquitin-conjugating enzyme E2 N measurement http://www.ebi.ac.uk/efo/EFO_0020841 GCST90250069 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-conjugating enzyme E2 T levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ubiquitin-conjugating enzyme E2 T measurement http://www.ebi.ac.uk/efo/EFO_0803217 GCST90250070 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-protein ligase E3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250071 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-like protein 4A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquitin-like protein 4A measurement http://www.ebi.ac.uk/efo/EFO_0802183 GCST90250072 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250073 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250074 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase 21 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ubiquitin carboxyl-terminal hydrolase 21 measurement http://www.ebi.ac.uk/efo/EFO_0802178 GCST90250075 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase 25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ubiquitin carboxyl-terminal hydrolase 25 measurement http://www.ebi.ac.uk/efo/EFO_0021881 GCST90250076 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase 28 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250077 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ubiquitin carboxyl-terminal hydrolase 8 measurement http://www.ebi.ac.uk/efo/EFO_0802179 GCST90250078 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250079 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquilin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquilin-4 measurement http://www.ebi.ac.uk/efo/EFO_0802177 GCST90250080 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin-associated and SH3 domain-containing protein B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250081 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ubiquitin domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802180 GCST90250082 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UBX domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 UBX domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0803219 GCST90250083 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UPF0729 protein C18orf32 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 UPF0729 protein C18orf32 measurement http://www.ebi.ac.uk/efo/EFO_0803236 GCST90250084 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. UPF0696 protein C11orf68 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 UPF0696 protein C11orf68 measurement http://www.ebi.ac.uk/efo/EFO_0802202 GCST90250085 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase isozyme L1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ubiquitin carboxyl-terminal hydrolase isozyme L1 measurement http://www.ebi.ac.uk/efo/EFO_0020838 GCST90250086 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ubiquitin carboxyl-terminal hydrolase isozyme L5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250087 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP four-disulfide core domain protein 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 WAP four-disulfide core domain protein 13 measurement http://www.ebi.ac.uk/efo/EFO_0803262 GCST90250204 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP four-disulfide core domain protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250205 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP four-disulfide core domain protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 WAP four-disulfide core domain protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802220 GCST90250206 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP four-disulfide core domain protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 WAP four-disulfide core domain protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0803264 GCST90250207 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP four-disulfide core domain protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250208 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP four-disulfide core domain protein 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250209 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP, kazal, immunoglobulin, kunitz and NTR domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 wap, kazal, immunoglobulin, kunitz and ntr domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020852 GCST90250210 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90250211 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Wnt inhibitory factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 wnt inhibitory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020853 GCST90250212 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WNT1-inducible-signaling pathway protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 WNT1-inducible-signaling pathway protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008321 GCST90250213 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WNT1-inducible-signaling pathway protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250214 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WNT1-inducible-signaling pathway protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 WNT1-inducible-signaling pathway protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0022003 GCST90250215 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Wnt-10a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250216 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Wnt-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250217 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Wnt-3a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250218 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Wnt-5a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250219 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein Wnt-7a levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein wnt-7a measurement http://www.ebi.ac.uk/efo/EFO_0020689 GCST90250220 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATPase WRNIP1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250221 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. WW domain-containing oxidoreductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250222 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA repair protein XRCC1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DNA repair protein XRCC1 measurement http://www.ebi.ac.uk/efo/EFO_0802479 GCST90250223 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA repair protein XRCC4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 DNA repair protein XRCC4 measurement http://www.ebi.ac.uk/efo/EFO_0801532 GCST90250224 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. X-ray repair cross-complementing protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 x-ray repair cross-complementing protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020855 GCST90250225 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Xyloside xylosyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 xyloside xylosyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802223 GCST90250226 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Y-box-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 y-box-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802224 GCST90250227 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. YEATS domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250228 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase ZNRF3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 E3 ubiquitin-protein ligase ZNRF3 measurement http://www.ebi.ac.uk/efo/EFO_0021943 GCST90250254 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc transporter 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 zinc transporter 3 measurement http://www.ebi.ac.uk/efo/EFO_0803287 GCST90250255 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc transporter 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 zinc transporter 5 measurement http://www.ebi.ac.uk/efo/EFO_0803288 GCST90250256 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zona pellucida-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250257 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zona pellucida-binding protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250258 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zona pellucida-like domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zona pellucida-like domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803290 GCST90250259 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zona pellucida sperm-binding protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zona pellucida sperm-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802229 GCST90250260 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ZW10 interactor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250261 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein zwilch homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250262 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Casein kinase II 2-alpha':2-beta heterotetramer levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 casein kinase II 2-alpha':2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020237 GCST90266937 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Activin B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90266938 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Inhibin beta B chain (mixed) levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90266939 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM3D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90247537 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pseudokinase FAM20A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pseudokinase FAM20A measurement http://www.ebi.ac.uk/efo/EFO_0801979 GCST90247538 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM49B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247539 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein FAM69C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247540 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fumarylacetoacetase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 fumarylacetoacetase measurement http://www.ebi.ac.uk/efo/EFO_0801609 GCST90247541 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fatty acid-binding protein 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247542 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fatty acid-binding protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247543 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. F-actin-capping protein subunit alpha-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247544 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. FAS-associated death domain protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247545 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fatty acid-binding protein, epidermal levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fatty acid-binding protein, epidermal measurement http://www.ebi.ac.uk/efo/EFO_0020372 GCST90247546 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Acylpyruvase FAHD1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247547 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fatty acid-binding protein, heart levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 fatty acid-binding protein, heart measurement http://www.ebi.ac.uk/efo/EFO_0020373 GCST90247548 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Fas apoptotic inhibitory molecule 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247549 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein YIPF6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein YIPF6 measurement http://www.ebi.ac.uk/efo/EFO_0802969 GCST90250229 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. YTH domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 YTH domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803268 GCST90250230 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AN1-type zinc finger protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250231 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. AN1-type zinc finger protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250232 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zymogen granule protein 16 homolog B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250233 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc fingers and homeoboxes protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250234 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc fingers and homeoboxes protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 zinc fingers and homeoboxes protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0803299 GCST90250235 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 zinc finger protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0803270 GCST90250236 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 134 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 134 measurement http://www.ebi.ac.uk/efo/EFO_0803271 GCST90250237 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 175 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 zinc finger protein 175 measurement http://www.ebi.ac.uk/efo/EFO_0802225 GCST90250238 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 18 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 zinc finger protein 18 measurement http://www.ebi.ac.uk/efo/EFO_0802226 GCST90250239 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 180 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 zinc finger protein 180 measurement http://www.ebi.ac.uk/efo/EFO_0803273 GCST90250240 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 23 measurement http://www.ebi.ac.uk/efo/EFO_0803274 GCST90250241 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 264 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 264 measurement http://www.ebi.ac.uk/efo/EFO_0803275 GCST90250242 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 275 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250243 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 276 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 zinc finger protein 276 measurement http://www.ebi.ac.uk/efo/EFO_0802227 GCST90250244 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 329 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 329 measurement http://www.ebi.ac.uk/efo/EFO_0803276 GCST90250245 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 334 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 zinc finger protein 334 measurement http://www.ebi.ac.uk/efo/EFO_0803277 GCST90250246 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 410 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 410 measurement http://www.ebi.ac.uk/efo/EFO_0803280 GCST90250247 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 526 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250248 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 566 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 566 measurement http://www.ebi.ac.uk/efo/EFO_0803282 GCST90250249 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 75D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 75D measurement http://www.ebi.ac.uk/efo/EFO_0803283 GCST90250250 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 774 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 zinc finger protein 774 measurement http://www.ebi.ac.uk/efo/EFO_0803284 GCST90250251 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc-alpha-2-glycoprotein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 zinc-alpha-2-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0802228 GCST90250252 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Zinc finger protein 34 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90250253 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Pyruvate carboxylase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 pyruvate carboxylase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802986 GCST90248870 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248871 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protocadherin-10 measurement http://www.ebi.ac.uk/efo/EFO_0801978 GCST90248872 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Programmed cell death 1 ligand 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90248873 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Programmed cell death 1 ligand 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 programmed cell death 1 ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0008268 GCST90248874 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248875 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin-9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protocadherin-9 measurement http://www.ebi.ac.uk/efo/EFO_0802975 GCST90248876 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin alpha-C1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248877 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin alpha-C2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protocadherin alpha-C2 measurement http://www.ebi.ac.uk/efo/EFO_0802971 GCST90248878 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin alpha-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protocadherin alpha-4 measurement http://www.ebi.ac.uk/efo/EFO_0801972 GCST90248879 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin alpha-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protocadherin alpha-7 measurement http://www.ebi.ac.uk/efo/EFO_0801973 GCST90248880 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin beta-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protocadherin beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0802972 GCST90248881 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin beta-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protocadherin beta-10 measurement http://www.ebi.ac.uk/efo/EFO_0801974 GCST90248882 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin beta-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protocadherin beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0801975 GCST90248883 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin beta-7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248884 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin gamma-A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248885 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin gamma-A10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248886 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin gamma-A12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248887 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin gamma-A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248888 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin gamma-B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248889 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protocadherin gamma-C3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248890 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein canopy homolog 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248891 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Plasma serine protease inhibitor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 plasma serine protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0020642 GCST90248892 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Phosphoenolpyruvate carboxykinase, cytosolic [GTP] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248893 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Procollagen C-endopeptidase enhancer 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 procollagen C-endopeptidase enhancer 1 measurement http://www.ebi.ac.uk/efo/EFO_0801920 GCST90248894 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation factor Xa levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 coagulation factor XA measurement http://www.ebi.ac.uk/efo/EFO_0020266 GCST90247102 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation Factor XI levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247103 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation factor XIII levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247104 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation factor XIII B chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247105 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cochlin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 10 cochlin measurement http://www.ebi.ac.uk/efo/EFO_0801481 GCST90247106 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cofilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247107 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Colipase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 colipase measurement http://www.ebi.ac.uk/efo/EFO_0801485 GCST90247108 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Colipase-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247109 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Colipase-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 colipase-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802417 GCST90247110 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen Type II levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247111 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen Type III levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247112 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagenase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 collagenase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020271 GCST90247113 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collectin-10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 collectin-10 measurement http://www.ebi.ac.uk/efo/EFO_0801491 GCST90247114 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collectin-11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90247115 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collectin-12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90247116 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. COMM domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 COMM domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802424 GCST90247117 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. COMM domain-containing protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 COMM domain-containing protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020273 GCST90247118 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. COMM domain-containing protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247119 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cartilage oligomeric matrix protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247120 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Catechol O-methyltransferase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247121 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Contactin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 contactin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020286 GCST90247122 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Contactin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90247123 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Contactin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 contactin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020287 GCST90247124 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Contactin-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 contactin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008101 GCST90247125 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. COP9 signalosome complex subunit 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 COP9 signalosome complex subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0801497 GCST90247126 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbohydrate sulfotransferase 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 carbohydrate sulfotransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0802368 GCST90247027 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carbohydrate sulfotransferase 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 carbohydrate sulfotransferase 9 measurement http://www.ebi.ac.uk/efo/EFO_0801449 GCST90247028 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chymotrypsinogen B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 chymotrypsinogen B measurement http://www.ebi.ac.uk/efo/EFO_0801477 GCST90247029 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chymotrypsinogen B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247030 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chymase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 chymase measurement http://www.ebi.ac.uk/efo/EFO_0020259 GCST90247031 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cilia- and flagella-associated protein 45 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cilia- and flagella-associated protein 45 measurement http://www.ebi.ac.uk/efo/EFO_0802401 GCST90247032 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cold-inducible RNA-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cold-inducible RNA-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801484 GCST90247033 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Casein kinase II 2-alpha:2-beta heterotetramer levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 casein kinase II 2-alpha:2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020236 GCST90247034 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Casein kinase II subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 casein kinase II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020238 GCST90247035 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Casein kinase II subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247036 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytoskeleton-associated protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cytoskeleton-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020309 GCST90247037 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytoskeleton-associated protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247038 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ck-beta-8-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 Ck-beta-8-1 measurement http://www.ebi.ac.uk/efo/EFO_0008085 GCST90247039 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Creatine kinase M-type:Creatine kinase B-type heterodimer levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 creatine kinase m-type:creatine kinase b-type heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020292 GCST90247040 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-dependent kinases regulatory subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247041 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Creatine kinase S-type, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247042 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Creatine kinase U-type, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247043 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-activated potassium channel subunit beta-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247044 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-activated chloride channel regulator 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247045 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium-activated chloride channel regulator 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247046 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 12 member A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-type lectin domain family 12 member A measurement http://www.ebi.ac.uk/efo/EFO_0801433 GCST90247047 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 1 member B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 C-type lectin domain family 1 member B measurement http://www.ebi.ac.uk/efo/EFO_0020200 GCST90247048 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 2 member A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-type lectin domain family 2 member A measurement http://www.ebi.ac.uk/efo/EFO_0802344 GCST90247049 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 2 member D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 C-type lectin domain family 2 member D measurement http://www.ebi.ac.uk/efo/EFO_0801434 GCST90247050 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 2 member L levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-type lectin domain family 2 member L measurement http://www.ebi.ac.uk/efo/EFO_0802346 GCST90247051 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. COP9 signalosome complex subunit 7b levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247127 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coatomer subunit epsilon levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247128 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Copine-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90247129 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Core-binding factor subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 core-binding factor subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801498 GCST90247130 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Corneodesmosin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 corneodesmosin measurement http://www.ebi.ac.uk/efo/EFO_0801499 GCST90247131 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cornulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247132 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Corticoliberin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 corticoliberin measurement http://www.ebi.ac.uk/efo/EFO_0802430 GCST90247133 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Corticosteroid-binding globulin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247134 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Corticotropin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 corticotropin measurement http://www.ebi.ac.uk/efo/EFO_0020289 GCST90247135 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome c oxidase subunit 4 isoform 2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cytochrome c oxidase subunit 4 isoform 2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801514 GCST90247136 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome c oxidase subunit 5A, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247137 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome c oxidase subunit 5B, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cytochrome c oxidase subunit 5B, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802449 GCST90247138 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome c oxidase subunit 6C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 cytochrome c oxidase subunit 6C measurement http://www.ebi.ac.uk/efo/EFO_0801515 GCST90247139 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytosolic purine 5-nucleotidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247140 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calpain small subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247141 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carnitine O-palmitoyltransferase 1, muscle isoform levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247142 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable serine carboxypeptidase CPVL levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 probable serine carboxypeptidase CPVL measurement http://www.ebi.ac.uk/efo/EFO_0801919 GCST90247143 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclic AMP-responsive element-binding protein 3-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cyclic AMP-responsive element-binding protein 3-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802439 GCST90247144 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclic AMP-responsive element-binding protein 3-like protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 cyclic AMP-responsive element-binding protein 3-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801506 GCST90247145 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cartilage acidic protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247146 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Death domain-containing protein CRADD levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247147 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytokine receptor common subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cytokine receptor common subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801518 GCST90247148 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytokine receptor common subunit gamma levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cytokine receptor common subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0020304 GCST90247149 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chordin-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 chordin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020257 GCST90247150 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chordin-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 chordin-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801474 GCST90247151 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chondroitin sulfate proteoglycan 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 chondroitin sulfate proteoglycan 4 measurement http://www.ebi.ac.uk/efo/EFO_0802394 GCST90247178 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine and glycine-rich protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247179 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine and glycine-rich protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cysteine and glycine-rich protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802444 GCST90247180 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cas scaffolding protein family member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cas scaffolding protein family member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802371 GCST90247181 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Connective tissue-activating peptide III levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 connective tissue-activating peptide III measurement http://www.ebi.ac.uk/efo/EFO_0020285 GCST90247182 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-terminal-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247183 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen triple helix repeat-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247184 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine--tRNA ligase, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cysteine--tRNA ligase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0802445 GCST90247185 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chymotrypsin-C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 chymotrypsin-C measurement http://www.ebi.ac.uk/efo/EFO_0802398 GCST90247186 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chymotrypsin-like protease CTRL-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 chymotrypsin-like protease CTRL-1 measurement http://www.ebi.ac.uk/efo/EFO_0801476 GCST90247187 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. cubilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cubilin measurement http://www.ebi.ac.uk/efo/EFO_0802433 GCST90247188 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cullin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247189 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cullin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cullin-3 measurement http://www.ebi.ac.uk/efo/EFO_0802435 GCST90247190 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cullin-4B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cullin-4B measurement http://www.ebi.ac.uk/efo/EFO_0802436 GCST90247191 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cullin-9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cullin-9 measurement http://www.ebi.ac.uk/efo/EFO_0802437 GCST90247192 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium uptake protein 2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247193 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcium uptake protein 3, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calcium uptake protein 3, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802355 GCST90247194 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Copper homeostasis protein cutC homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247195 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CUB and zona pellucida-like domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CUB and zona pellucida-like domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803309 GCST90247196 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Extracellular superoxide dismutase [Cu-Zn] levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247197 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cancer/testis antigen 55 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cancer/testis antigen 55 measurement http://www.ebi.ac.uk/efo/EFO_0802365 GCST90247198 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome c oxidase subunit 7A1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cytochrome c oxidase subunit 7A1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802450 GCST90247199 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CXADR-like membrane protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CXADR-like membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0801504 GCST90247200 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST90247201 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Casein kinase I isoform gamma-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 casein kinase I isoform gamma-2 measurement http://www.ebi.ac.uk/efo/EFO_0801458 GCST90247177 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein dpy-30 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein dpy-30 homolog measurement http://www.ebi.ac.uk/efo/EFO_0802933 GCST90247352 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dihydropyrimidinase-related protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 dihydropyrimidinase-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802467 GCST90247353 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dihydropyrimidinase-related protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dihydropyrimidinase-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802468 GCST90247354 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Draxin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247355 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Developmentally-regulated GTP-binding protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247356 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dorsal root ganglia homeobox protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dorsal root ganglia homeobox protein measurement http://www.ebi.ac.uk/efo/EFO_0801545 GCST90247357 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desmocollin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247358 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desmocollin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 desmocollin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021936 GCST90247359 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desmocollin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 desmocollin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020320 GCST90247360 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Down syndrome cell adhesion molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 down syndrome cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0022028 GCST90247361 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Double-stranded RNA-binding protein Staufen homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 double-stranded RNA-binding protein Staufen homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0801546 GCST90247362 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Double-stranded RNA-binding protein Staufen homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 double-stranded RNA-binding protein Staufen homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0801547 GCST90247363 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. D-tyrosyl-tRNA(Tyr) deacylase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247364 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase DTX1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 E3 ubiquitin-protein ligase DTX1 measurement http://www.ebi.ac.uk/efo/EFO_0802503 GCST90247365 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. E3 ubiquitin-protein ligase DTX3L levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 E3 ubiquitin-protein ligase DTX3L measurement http://www.ebi.ac.uk/efo/EFO_0801553 GCST90247366 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein phosphatase 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dual specificity protein phosphatase 15 measurement http://www.ebi.ac.uk/efo/EFO_0802494 GCST90247367 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein phosphatase 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 dual specificity protein phosphatase 16 measurement http://www.ebi.ac.uk/efo/EFO_0802495 GCST90247368 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein phosphatase 23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247369 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein phosphatase 26 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247370 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity phosphatase 28 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247371 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein phosphatase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 dual specificity protein phosphatase 4 measurement http://www.ebi.ac.uk/efo/EFO_0801550 GCST90247372 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein phosphatase 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dual specificity protein phosphatase 6 measurement http://www.ebi.ac.uk/efo/EFO_0802496 GCST90247373 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein phosphatase 13 isoform A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 dual specificity protein phosphatase 13 isoform A measurement http://www.ebi.ac.uk/efo/EFO_0801549 GCST90247374 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Segment polarity protein dishevelled homolog DVL-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 segment polarity protein dishevelled homolog DVL-2 measurement http://www.ebi.ac.uk/efo/EFO_0802044 GCST90247375 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynein light chain Tctex-type 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247376 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynactin subunit 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 dynactin subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0020338 GCST90247379 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynorphin A (1-17) levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247380 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dihydrofolate reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 dihydrofolate reductase measurement http://www.ebi.ac.uk/efo/EFO_0801526 GCST90247381 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity tyrosine-phosphorylation-regulated kinase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 dual specificity tyrosine-phosphorylation-regulated kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020337 GCST90247382 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Band 4.1-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247383 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynein light chain Tctex-type 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 dynein light chain Tctex-type 3 measurement http://www.ebi.ac.uk/efo/EFO_0802497 GCST90247377 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynamin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247378 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin-B1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ephrin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0021930 GCST90247402 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin-B2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ephrin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0802526 GCST90247403 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin-B3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90247404 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Embryonal Fyn-associated substrate levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247405 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epidermal growth factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90247406 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EGF-containing fibulin-like extracellular matrix protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 EGF-containing fibulin-like extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0022022 GCST90247407 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Epidermal growth factor-like protein 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247408 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. L-selectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90248341 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lutropin subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lutropin subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0801773 GCST90248342 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Leukocyte-specific transcript 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 leukocyte-specific transcript 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802707 GCST90248343 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Latent-transforming growth factor beta-binding protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 latent-transforming growth factor beta-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021940 GCST90248344 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphokine-activated killer T-cell-originated protein kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248345 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lumican levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 lumican measurement http://www.ebi.ac.uk/efo/EFO_0021889 GCST90248346 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lupus La protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lupus La protein measurement http://www.ebi.ac.uk/efo/EFO_0802713 GCST90248347 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Luteinizing hormone levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90248348 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Isoform L-VEGF165 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248349 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. L-xylulose reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248350 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphocyte antigen 6 complex locus protein G6c levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lymphocyte antigen 6 complex locus protein G6c measurement http://www.ebi.ac.uk/efo/EFO_0801774 GCST90248351 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphocyte antigen 75 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248352 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphotoxin-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lymphotoxin-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020544 GCST90248353 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphotoxin alpha2:beta1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 lymphotoxin alpha2:beta1 measurement http://www.ebi.ac.uk/efo/EFO_0020543 GCST90248354 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphotoxin alpha1:beta2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lymphotoxin alpha1:beta2 measurement http://www.ebi.ac.uk/efo/EFO_0020542 GCST90248355 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ly6/PLAUR domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 Ly6/PLAUR domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0021931 GCST90248356 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysophospholipase-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 lysophospholipase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0802719 GCST90248357 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysosomal alpha-glucosidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248358 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelin-converting enzyme 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90247384 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelin-converting enzyme-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247385 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Enoyl-CoA delta isomerase 1, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247386 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Enoyl-CoA delta isomerase 2, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247387 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Extracellular matrix protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008126 GCST90247388 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eosinophil cationic protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 eosinophil cationic protein measurement http://www.ebi.ac.uk/efo/EFO_0010913 GCST90247389 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelial cell-selective adhesion molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90247390 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ectodysplasin-A, secreted form levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 ectodysplasin-a, secreted form measurement http://www.ebi.ac.uk/efo/EFO_0020341 GCST90247391 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Enhancer of mRNA-decapping protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 enhancer of mRNA-decapping protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802523 GCST90247392 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endothelial differentiation-related factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 endothelial differentiation-related factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801571 GCST90247393 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EGF-like repeat and discoidin I-like domain-containing protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247394 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Early endosome antigen 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 early endosome antigen 1 measurement http://www.ebi.ac.uk/efo/EFO_0802514 GCST90247395 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Elongation factor 1-delta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247396 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Eukaryotic elongation factor 2 kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247397 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EF-hand calcium-binding domain-containing protein 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 EF-hand calcium-binding domain-containing protein 14 measurement http://www.ebi.ac.uk/efo/EFO_0802518 GCST90247398 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. EF-hand domain-containing protein D1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247399 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin-A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 ephrin-A2 measurement http://www.ebi.ac.uk/efo/EFO_0021944 GCST90247400 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ephrin-A5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ephrin-A5 measurement http://www.ebi.ac.uk/efo/EFO_0020357 GCST90247401 Genome-wide genotyping array 2023-08-11 37040585 Li L 2023-04-11 Menopause www.ncbi.nlm.nih.gov/pubmed/37040585 Interactions between genetic variants and environmental risk factors are associated with the severity of pelvic organ prolapse. Pelvic organ prolapse 707 Han Chinese ancestry females NA Affymetrix, Illumina [640674] (imputed) 4 pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004710 GCST90277420 Genome-wide genotyping array 2023-08-11 37040585 Li L 2023-04-11 Menopause www.ncbi.nlm.nih.gov/pubmed/37040585 Interactions between genetic variants and environmental risk factors are associated with the severity of pelvic organ prolapse. Pelvic organ prolapse x maximum birth weight interaction 608 Han Chinese ancestry females NA Affymetrix, Illumina [640674] (imputed) 37 birth weight, pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0004344, http://www.ebi.ac.uk/efo/EFO_0004710 GCST90277421 Genome-wide genotyping array 2023-08-11 37040585 Li L 2023-04-11 Menopause www.ncbi.nlm.nih.gov/pubmed/37040585 Interactions between genetic variants and environmental risk factors are associated with the severity of pelvic organ prolapse. Pelvic organ prolapse x age interaction 707 Han Chinese ancestry females NA Affymetrix, Illumina [640674] (imputed) 32 age at assessment, pelvic organ prolapse http://www.ebi.ac.uk/efo/EFO_0008007, http://www.ebi.ac.uk/efo/EFO_0004710 GCST90277422 Genome-wide genotyping array 2023-08-10 36869765 Davidsson P 2023-03-03 Cardiovasc Res www.ncbi.nlm.nih.gov/pubmed/36869765 VEGF-D plasma levels and VEGFD genetic variants are independently associated with outcomes in patients with cardiovascular disease. vascular endothelial growth factor D levels 1,907 European ancestry individuals with acute coronary syndrome, 20 black individuals with acute coronary syndrome, 39 Asian ancestry individuals with acute coronary syndrome 2,944 individuals with chronic coronary syndrome Illumina [NR] (imputed) 2 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90277419 Genome-wide genotyping array 2023-08-09 36448302 Jokubaitis VG 2022-11-30 Brain www.ncbi.nlm.nih.gov/pubmed/36448302 Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity. Median relapse-independent longitudinal age-related multiple sclerosis severity score in relapse-onset multiple sclerosis 1,813 European ancestry individuals NA Illumina [5985626] (imputed) 14 multiple sclerosis symptom measurement http://www.ebi.ac.uk/efo/EFO_0803536 GCST90274850 Genome-wide genotyping array 2023-08-09 36448302 Jokubaitis VG 2022-11-30 Brain www.ncbi.nlm.nih.gov/pubmed/36448302 Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity. Median relapse-independent longitudinal age-related multiple sclerosis severity score in relapse-onset multiple sclerosis 500 European ancestry men NA Illumina [5985626] (imputed) 5 multiple sclerosis symptom measurement http://www.ebi.ac.uk/efo/EFO_0803536 GCST90274851 Genome-wide genotyping array 2023-08-09 36448302 Jokubaitis VG 2022-11-30 Brain www.ncbi.nlm.nih.gov/pubmed/36448302 Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity. Median relapse-independent longitudinal age-related multiple sclerosis severity score in relapse-onset multiple sclerosis 1,313 European ancestry women NA Illumina [5985626] (imputed) 4 multiple sclerosis symptom measurement http://www.ebi.ac.uk/efo/EFO_0803536 GCST90274852 Genome-wide genotyping array 2023-08-09 36448302 Jokubaitis VG 2022-11-30 Brain www.ncbi.nlm.nih.gov/pubmed/36448302 Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity. Median relapse-independent longitudinal Multiple Sclerosis Severity Scale score in relapse-onset multiple sclerosis 1,813 European ancestry individuals NA Illumina [5985626] (imputed) 11 multiple sclerosis symptom measurement http://www.ebi.ac.uk/efo/EFO_0803536 GCST90274853 Genome-wide genotyping array 2023-08-09 36448302 Jokubaitis VG 2022-11-30 Brain www.ncbi.nlm.nih.gov/pubmed/36448302 Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity. Median relapse-independent longitudinal Multiple Sclerosis Severity Scale score in relapse-onset multiple sclerosis 500 European ancestry men NA Illumina [5985626] (imputed) 4 multiple sclerosis symptom measurement http://www.ebi.ac.uk/efo/EFO_0803536 GCST90274854 Genome-wide genotyping array 2023-08-09 36448302 Jokubaitis VG 2022-11-30 Brain www.ncbi.nlm.nih.gov/pubmed/36448302 Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity. Median relapse-independent longitudinal Multiple Sclerosis Severity Scale score in relapse-onset multiple sclerosis 1,313 European ancestry women NA Illumina [5985626] (imputed) 4 multiple sclerosis symptom measurement http://www.ebi.ac.uk/efo/EFO_0803536 GCST90274855 Genome-wide genotyping array 2023-08-09 36448302 Jokubaitis VG 2022-11-30 Brain www.ncbi.nlm.nih.gov/pubmed/36448302 Not all roads lead to the immune system: the genetic basis of multiple sclerosis severity. Multiple sclerosis (age of onset) 1,813 European ancestry individuals NA Illumina [5985626] (imputed) 9 age of onset of multiple sclerosis http://purl.obolibrary.org/obo/OBA_2001029 GCST90274856 Genome-wide genotyping array 2023-08-21 37174278 Graham CA 2023-04-22 Foods www.ncbi.nlm.nih.gov/pubmed/37174278 Regulator of G-Protein Signalling 9: A New Candidate Gene for Sweet Food Liking? Sweet food liking 1,482 Italian ancestry individuals 1,073 Italian ancestry individuals Illumina [NR] (imputed) 16 sweet liking measurement http://www.ebi.ac.uk/efo/EFO_0010156 GCST90277987 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in small HDL (UKB data field 23575) 88,329 European ancestry individuals NA NR [16366144] (imputed) 25 cholesterol in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022226 GCST90269672 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in small HDL (UKB data field 23576) 88,329 European ancestry individuals NA NR [16366144] (imputed) 24 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269673 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in small HDL (UKB data field 23577) 88,329 European ancestry individuals NA NR [16366144] (imputed) 26 free cholesterol in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022270 GCST90269674 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in small HDL (UKB data field 23578) 88,329 European ancestry individuals NA NR [16366144] (imputed) 48 triglycerides in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022158 GCST90269675 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in chylomicrons and extremely large VLDL percentage (UKB data field 23579) 85,701 European ancestry individuals NA NR [16364468] (imputed) 21 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269676 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in chylomicrons and extremely large VLDL percentage (UKB data field 23580) 85,701 European ancestry individuals NA NR [16364468] (imputed) 14 cholesterol to total lipids in chylomicrons and extremely large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022232 GCST90269677 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in chylomicrons and extremely large VLDL percentage (UKB data field 23581) 85,701 European ancestry individuals NA NR [16364468] (imputed) 16 cholesteryl esters to total lipids in chylomicrons and extremely large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022246 GCST90269678 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in chylomicrons and extremely large VLDL percentage (UKB data field 23582) 85,701 European ancestry individuals NA NR [16364468] (imputed) 16 free cholesterol to total lipids in chylomicrons and extremely large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022277 GCST90269679 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in chylomicrons and extremely large VLDL percentage (UKB data field 23583) 85,701 European ancestry individuals NA NR [16364468] (imputed) 13 triglycerides to total lipids in chylomicrons and extremely large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022328 GCST90269680 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in very large VLDL percentage (UKB data field 23584) 87,620 European ancestry individuals NA NR [16365834] (imputed) 30 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269681 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in very large VLDL percentage (UKB data field 23585) 87,620 European ancestry individuals NA NR [16365834] (imputed) 39 cholesterol to total lipids in very large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022244 GCST90269682 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in very large VLDL percentage (UKB data field 23586) 87,620 European ancestry individuals NA NR [16365834] (imputed) 40 cholesteryl esters to total lipids in very large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022258 GCST90269683 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in very large VLDL percentage (UKB data field 23587) 87,620 European ancestry individuals NA NR [16365834] (imputed) 38 free cholesterol to total lipids in very large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022289 GCST90269684 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in very large VLDL percentage (UKB data field 23588) 87,620 European ancestry individuals NA NR [16365834] (imputed) 37 triglycerides to total lipids in very large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022340 GCST90269685 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in large VLDL percentage (UKB data field 23589) 88,321 European ancestry individuals NA NR [16366100] (imputed) 44 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269686 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in large VLDL percentage (UKB data field 23590) 88,321 European ancestry individuals NA NR [16366100] (imputed) 33 cholesterol to total lipids in large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022236 GCST90269687 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in large VLDL percentage (UKB data field 23591) 88,321 European ancestry individuals NA NR [16366100] (imputed) 39 cholesteryl esters to total lipids in large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022250 GCST90269688 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in large VLDL percentage (UKB data field 23592) 88,321 European ancestry individuals NA NR [16366100] (imputed) 29 free cholesterol to total lipids in large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022281 GCST90269689 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in large VLDL percentage (UKB data field 23593) 88,321 European ancestry individuals NA NR [16366100] (imputed) 29 triglycerides to total lipids in large VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022332 GCST90269690 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in medium VLDL percentage (UKB data field 23594) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269691 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in medium VLDL percentage (UKB data field 23595) 88,329 European ancestry individuals NA NR [16366144] (imputed) 50 cholesterol to total lipids in medium VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022239 GCST90269692 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in medium VLDL percentage (UKB data field 23596) 88,329 European ancestry individuals NA NR [16366144] (imputed) 51 cholesteryl esters to total lipids in medium VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022253 GCST90269693 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in medium VLDL percentage (UKB data field 23597) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 free cholesterol to total lipids in medium VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022284 GCST90269694 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in medium VLDL percentage (UKB data field 23598) 88,329 European ancestry individuals NA NR [16366144] (imputed) 48 triglycerides to total lipids in medium VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022335 GCST90269695 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in small VLDL percentage (UKB data field 23599) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269696 Genome-wide genotyping array 2023-06-21 36773317 Butler-Laporte G 2023-02-11 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/36773317 Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach. Ferritin levels 270,794 European ancestry individuals NA NR [10519191] (imputed) 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90270865 Genome-wide genotyping array 2023-06-21 36773317 Butler-Laporte G 2023-02-11 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/36773317 Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach. Any infection (hospital admission) 123,508 European ancestry cases, 577,141 European ancestry controls NA NR [11762722] (imputed) 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90270866 Genome-wide genotyping array 2023-06-21 36773317 Butler-Laporte G 2023-02-11 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/36773317 Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach. Urinary tract infection (hospital admission) 21,812 European ancestry cases, 418,432 European ancestry controls NA NR [11762723] (imputed) 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90270867 Genome-wide genotyping array 2023-06-21 36773317 Butler-Laporte G 2023-02-11 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/36773317 Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach. Skin and soft tissue infections (hospital admission) 29,247 European ancestry cases, 671,402 European ancestry controls NA NR [11762724] (imputed) 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90270868 Genome-wide genotyping array 2023-06-21 36773317 Butler-Laporte G 2023-02-11 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/36773317 Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach. Pneumonia (hospital admission) 55,241 European ancestry cases, 645,408 European ancestry controls NA NR [11762725] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90270869 Genome-wide genotyping array 2023-06-21 36773317 Butler-Laporte G 2023-02-11 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/36773317 Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach. Candida infection (hospital admission) 7,286 European ancestry cases, 690,977 European ancestry controls NA NR [11762726] (imputed) 0 candidiasis http://purl.obolibrary.org/obo/MONDO_0002026 GCST90270870 Genome-wide genotyping array 2023-06-21 36773317 Butler-Laporte G 2023-02-11 Int J Epidemiol www.ncbi.nlm.nih.gov/pubmed/36773317 Increasing serum iron levels and their role in the risk of infectious diseases: a Mendelian randomization approach. Sepsis (hospital admission) 18,931 European ancestry cases, 663,531 European ancestry controls NA NR [11762727] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90270871 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Serum alpha-fetoprotein levels 427 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 0 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST90103741 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Serum cancer antigen 50 (CA 50) levels 265 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 0 cancer antigen 50 measurement http://www.ebi.ac.uk/efo/EFO_0020994 GCST90103742 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Serum cancer antigen 125 (CA 125) levels 424 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 0 cancer antigen 125 measurement http://www.ebi.ac.uk/efo/EFO_0010603 GCST90103743 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Serum cancer antigen 15.3 levels 165 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 1 cancer antigen 15.3 measurement http://www.ebi.ac.uk/efo/EFO_0010585 GCST90103744 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Serum cancer antigen 19.9 levels 415 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 0 cancer antigen 19.9 measurement http://www.ebi.ac.uk/efo/EFO_0010584 GCST90103745 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Serum carcinoembryonic antigen levels 424 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 0 serum carcinoembryonic antigen measurement http://www.ebi.ac.uk/efo/EFO_0005760 GCST90103746 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Serum prostate-specific antigen levels 233 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 0 prostate-specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0020660 GCST90103747 Genome-wide genotyping array 2023-11-10 35144566 Li X 2022-02-10 BMC Cancer www.ncbi.nlm.nih.gov/pubmed/35144566 Genome-wide association study of serum tumor markers in Southern Chinese Han population. Squamous cell carcinoma antigen (SCCA) levels 422 Han Chinese ancestry individuals 398 Han Chinese ancestry individuals NR [6423076] (imputed) 0 squamous cell carcinoma antigen measurement http://www.ebi.ac.uk/efo/EFO_0020995 GCST90103748 Genome-wide genotyping array 2023-05-15 37148359 Huerta-Chagoya A 2023-05-06 Diabetologia www.ncbi.nlm.nih.gov/pubmed/37148359 The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes. Type 2 diabetes (adjusted for BMI) 8,150 Hispanic or Latin American cases, 10,735 Hispanic or Latin American controls 13,617 Hispanic or Latin American cases, 20,822 Hispanic or Latin American controls Affymetrix, Illumina [68826018] (imputed) 21 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90255648 Genome-wide genotyping array, Exome-wide sequencing [Illumina Omni 2.5 array | Illumina Sure-Select Human All Exon v2.0 | Illumina G4L | Illumina MEGA array | Affymetrix Axiom] 2023-08-15 37538507 Burley K 2023-05-14 Res Pract Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/37538507 PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry. Platelet count 20,218 Bangladeshi ancestry individuals NA Illumina [19197360] (imputed) 22 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90271311 Genome-wide genotyping array 2023-08-15 37538507 Burley K 2023-05-14 Res Pract Thromb Haemost www.ncbi.nlm.nih.gov/pubmed/37538507 PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry. Platelet count 9,198 Pakistani ancestry individuals NA Illumina [18317341] (imputed) 5 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90271312 Genome-wide genotyping array 2023-08-30 37127109 Zhang J 2023-04-29 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/37127109 Metabolic signature of healthy lifestyle and risk of rheumatoid arthritis: observational and Mendelian randomization study. Metabolic signature 86,675 European ancestry individuals NA Affymetrix [11470394] 42 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90278210 Genome-wide genotyping array 2023-06-27 36802911 Naito T 2023-02-21 Circulation www.ncbi.nlm.nih.gov/pubmed/36802911 Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Study. Primary aldosteronism 392 Japanese ancestry cases, 33,802 Japanese ancestry controls NA Illumina [8328861] (imputed) 12 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90271575 Genome-wide genotyping array 2023-06-27 36802911 Naito T 2023-02-21 Circulation www.ncbi.nlm.nih.gov/pubmed/36802911 Genetic Risk of Primary Aldosteronism and Its Contribution to Hypertension: A Cross-Ancestry Meta-Analysis of Genome-Wide Association Study. Primary aldosteronism 392 Japanese ancestry cases, 33,802 Japanese ancestry controls, 424 European ancestry cases, 391,437 European ancestry controls NA Affymetrix, Illumina [5508027] (imputed) 6 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90271576 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/14:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Sterol ester (27:1/14:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045188 GCST90244191 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/15:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Sterol ester (27:1/15:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045189 GCST90244192 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/16:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 5 level of Sterol ester (27:1/16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045191 GCST90244193 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/16:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Sterol ester (27:1/16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045190 GCST90244194 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/17:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Sterol ester (27:1/17:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045192 GCST90244195 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/17:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90244196 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Sterol ester (27:1/18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045196 GCST90244197 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Sterol ester (27:1/18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045195 GCST90244198 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Sterol ester (27:1/18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045194 GCST90244199 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Sterol ester (27:1/18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045193 GCST90244200 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Sterol ester (27:1/20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045200 GCST90244201 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Sterol ester (27:1/20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045199 GCST90244202 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 12 level of Sterol ester (27:1/20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045198 GCST90244203 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Sterol ester (27:1/20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045197 GCST90244204 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/22:6) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Sterol ester (27:1/22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045201 GCST90244205 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d40:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Ceramide (d40:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045185 GCST90244206 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d40:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Ceramide (d40:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045184 GCST90244207 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d42:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Ceramide (d42:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045187 GCST90244208 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d42:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Ceramide (d42:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045186 GCST90244209 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Cholesterol levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90244210 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (16:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Diacylglycerol (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045167 GCST90244211 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (16:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Diacylglycerol (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045168 GCST90244212 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (16:1_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Diacylglycerol (16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045169 GCST90244213 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (18:1_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Diacylglycerol (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045170 GCST90244214 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (18:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Diacylglycerol (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045171 GCST90244215 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylinositol (18:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045157 GCST90244316 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Phosphatidylinositol (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045158 GCST90244317 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:1_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylinositol (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045159 GCST90244318 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylinositol (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045160 GCST90244319 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:1_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylinositol (18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045161 GCST90244320 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d32:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 5 level of Sphingomyelin (d32:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045173 GCST90244321 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d34:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Sphingomyelin (d34:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045176 GCST90244322 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d34:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Sphingomyelin (d34:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045175 GCST90244323 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d34:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Sphingomyelin (d34:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045174 GCST90244324 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d36:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Sphingomyelin (d36:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045178 GCST90244325 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d36:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Sphingomyelin (d36:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045177 GCST90244326 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d38:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 8 level of Sphingomyelin (d38:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045180 GCST90244327 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d38:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Sphingomyelin (d38:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045179 GCST90244328 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d40:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 5 level of Sphingomyelin (d40:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045182 GCST90244329 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d40:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 5 level of Sphingomyelin (d40:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045181 GCST90244330 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d42:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 6 level of Sphingomyelin (d42:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045183 GCST90244331 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (46:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 46:1 measurement http://www.ebi.ac.uk/efo/EFO_0010401 GCST90244332 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (46:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 46:2 measurement http://www.ebi.ac.uk/efo/EFO_0010402 GCST90244333 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90244334 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90244335 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90244336 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90244337 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (49:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90244338 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (49:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Triacylglycerol (49:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045162 GCST90244339 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90244340 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045129 GCST90244291 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (O-18:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045130 GCST90244292 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (O-18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045131 GCST90244293 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_16:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:2_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045132 GCST90244294 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-18:2_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045133 GCST90244295 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045134 GCST90244296 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045135 GCST90244297 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (16:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 6 level of Phosphatidylethanolamine (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045136 GCST90244298 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (16:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 8 level of Phosphatidylethanolamine (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045137 GCST90244299 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 7 level of Phosphatidylethanolamine (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045139 GCST90244300 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 6 level of Phosphatidylethanolamine (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045140 GCST90244301 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:1_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Phosphatidylethanolamine (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045142 GCST90244302 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-16:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylethanolamine (O-16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045144 GCST90244303 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-16:1_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045145 GCST90244304 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-16:1_22:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylethanolamine (O-16:1_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045146 GCST90244305 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045147 GCST90244306 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:1_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045148 GCST90244307 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:2_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:2_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045149 GCST90244308 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:2_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045150 GCST90244309 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:2_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045151 GCST90244310 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (16:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylinositol (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045152 GCST90244311 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (16:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylinositol (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045153 GCST90244312 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (16:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylinositol (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045154 GCST90244313 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylinositol (18:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045155 GCST90244314 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Phosphatidylinositol (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045156 GCST90244315 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (16:0_20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045077 GCST90244241 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_22:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (16:0_22:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045078 GCST90244242 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_22:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (16:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045079 GCST90244243 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_22:6) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (16:0_22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045080 GCST90244244 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_18:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (16:1_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045081 GCST90244245 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045082 GCST90244246 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045083 GCST90244247 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045084 GCST90244248 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (17:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (17:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045085 GCST90244249 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (17:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (17:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045086 GCST90244250 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (17:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 8 level of Phosphatidylcholine (17:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045087 GCST90244251 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045089 GCST90244252 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045090 GCST90244253 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_18:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:0_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045091 GCST90244254 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:0_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045092 GCST90244255 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045093 GCST90244256 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 8 level of Phosphatidylcholine (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045094 GCST90244257 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:0_20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045095 GCST90244258 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_22:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045096 GCST90244259 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_22:6) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:0_22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045097 GCST90244260 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045099 GCST90244261 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045100 GCST90244262 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_18:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:1_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045101 GCST90244263 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_20:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (18:1_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045102 GCST90244264 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045103 GCST90244265 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (18:1_18:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Diacylglycerol (18:1_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045172 GCST90244216 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (16:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045066 GCST90244217 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045088 GCST90244218 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:1_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045098 GCST90244219 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:2_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045105 GCST90244220 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (20:4_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (20:4_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045110 GCST90244221 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:0_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylethanolamine (18:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045138 GCST90244222 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:1_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of Phosphatidylethanolamine (18:1_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045141 GCST90244223 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:2_0:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (18:2_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045143 GCST90244224 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (14:0_16:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (14:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045061 GCST90244225 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (14:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (14:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045062 GCST90244226 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (14:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (14:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045063 GCST90244227 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (15:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (15:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045064 GCST90244228 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (15:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (15:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045065 GCST90244229 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_16:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (16:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045067 GCST90244230 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_16:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (16:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045068 GCST90244231 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_17:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90244232 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (16:0_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045069 GCST90244233 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045070 GCST90244234 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045071 GCST90244235 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (16:0_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045072 GCST90244236 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (16:0_20:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045073 GCST90244237 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (16:0_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045074 GCST90244238 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (16:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045075 GCST90244239 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 7 level of Phosphatidylcholine (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045076 GCST90244240 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 6 level of Phosphatidylcholine (18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045104 GCST90244266 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045106 GCST90244267 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_20:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:2_20:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045107 GCST90244268 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (18:2_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045108 GCST90244269 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045109 GCST90244270 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_16:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045111 GCST90244271 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_16:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045112 GCST90244272 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045113 GCST90244273 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045114 GCST90244274 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-16:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045115 GCST90244275 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045116 GCST90244276 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_22:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045117 GCST90244277 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_16:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:1_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045118 GCST90244278 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_18:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:1_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045119 GCST90244279 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_18:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045120 GCST90244280 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_18:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045121 GCST90244281 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_20:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045122 GCST90244282 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (O-16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045123 GCST90244283 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:2_18:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90244284 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-17:0_15:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-17:0_15:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045124 GCST90244285 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-17:0_17:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90244286 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:0_14:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:0_14:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045125 GCST90244287 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:0_16:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045126 GCST90244288 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:0_20:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045127 GCST90244289 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_16:0) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-18:1_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045128 GCST90244290 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:7) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 56:7 measurement http://www.ebi.ac.uk/efo/EFO_0010434 GCST90244366 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:8) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90244367 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (58:7) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 58:7 measurement http://www.ebi.ac.uk/efo/EFO_0010441 GCST90244368 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (58:8) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90244369 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/14:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Sterol ester (27:1/14:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045188 GCST90244370 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/15:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Sterol ester (27:1/15:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045189 GCST90244371 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/16:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 8 level of Sterol ester (27:1/16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045191 GCST90244372 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/16:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Sterol ester (27:1/16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045190 GCST90244373 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/17:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Sterol ester (27:1/17:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045192 GCST90244374 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/17:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90244375 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 9 level of Sterol ester (27:1/18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045196 GCST90244376 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 9 level of Sterol ester (27:1/18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045195 GCST90244377 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 13 level of Sterol ester (27:1/18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045194 GCST90244378 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/18:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Sterol ester (27:1/18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045193 GCST90244379 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Sterol ester (27:1/20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045200 GCST90244380 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 11 level of Sterol ester (27:1/20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045199 GCST90244381 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 14 level of Sterol ester (27:1/20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045198 GCST90244382 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/20:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 5 level of Sterol ester (27:1/20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045197 GCST90244383 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sterol ester (27:1/22:6) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Sterol ester (27:1/22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045201 GCST90244384 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d40:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Ceramide (d40:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045185 GCST90244385 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d40:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Ceramide (d40:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045184 GCST90244386 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d42:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 5 level of Ceramide (d42:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045187 GCST90244387 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Ceramide (d42:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Ceramide (d42:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045186 GCST90244388 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Cholesterol levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90244389 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (16:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Diacylglycerol (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045167 GCST90244390 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (16:0_20:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045073 GCST90244416 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (16:0_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045074 GCST90244417 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Phosphatidylcholine (16:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045075 GCST90244418 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 10 level of Phosphatidylcholine (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045076 GCST90244419 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_20:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (16:0_20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045077 GCST90244420 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_22:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (16:0_22:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045078 GCST90244421 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_22:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (16:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045079 GCST90244422 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_22:6) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (16:0_22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045080 GCST90244423 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_18:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (16:1_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045081 GCST90244424 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Phosphatidylcholine (16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045082 GCST90244425 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 9 level of Phosphatidylcholine (16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045083 GCST90244426 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:1_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045084 GCST90244427 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (17:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (17:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045085 GCST90244428 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (17:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (17:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045086 GCST90244429 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (17:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 10 level of Phosphatidylcholine (17:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045087 GCST90244430 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045089 GCST90244431 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Phosphatidylcholine (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045090 GCST90244432 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_18:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:0_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045091 GCST90244433 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (18:0_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045092 GCST90244434 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 11 level of Phosphatidylcholine (18:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045093 GCST90244435 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 13 level of Phosphatidylcholine (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045094 GCST90244436 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_20:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:0_20:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045095 GCST90244437 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_22:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (18:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045096 GCST90244438 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_22:6) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:0_22:6) in blood serum http://purl.obolibrary.org/obo/OBA_2045097 GCST90244439 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045099 GCST90244440 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (16:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Diacylglycerol (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045168 GCST90244391 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (16:1_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Diacylglycerol (16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045169 GCST90244392 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (18:1_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Diacylglycerol (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045170 GCST90244393 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (18:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 7 level of Diacylglycerol (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045171 GCST90244394 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Diacylglycerol (18:1_18:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Diacylglycerol (18:1_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045172 GCST90244395 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (16:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045066 GCST90244396 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:0_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045088 GCST90244397 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:1_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045098 GCST90244398 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:2_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045105 GCST90244399 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (20:4_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Phosphatidylcholine (20:4_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045110 GCST90244400 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:0_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylethanolamine (18:0_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045138 GCST90244401 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:1_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylethanolamine (18:1_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045141 GCST90244402 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:2_0:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 8 level of Phosphatidylethanolamine (18:2_0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045143 GCST90244403 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (14:0_16:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (14:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045061 GCST90244404 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (14:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (14:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045062 GCST90244405 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (14:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 11 level of Phosphatidylcholine (14:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045063 GCST90244406 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (15:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (15:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045064 GCST90244407 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (15:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 8 level of Phosphatidylcholine (15:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045065 GCST90244408 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_16:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (16:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045067 GCST90244409 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_16:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (16:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045068 GCST90244410 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_17:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90244411 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (16:0_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045069 GCST90244412 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Phosphatidylcholine (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045070 GCST90244413 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 13 level of Phosphatidylcholine (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045071 GCST90244414 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (16:0_18:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 7 level of Phosphatidylcholine (16:0_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045072 GCST90244415 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 7 level of Phosphatidylcholine (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045100 GCST90244441 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_18:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (18:1_18:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045101 GCST90244442 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_20:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 5 level of Phosphatidylcholine (18:1_20:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045102 GCST90244443 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045103 GCST90244444 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:1_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 8 level of Phosphatidylcholine (18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045104 GCST90244445 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045106 GCST90244446 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_20:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (18:2_20:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045107 GCST90244447 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (18:2_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045108 GCST90244448 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (18:2_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045109 GCST90244449 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_16:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:0_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045111 GCST90244450 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_16:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045112 GCST90244451 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045113 GCST90244452 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045114 GCST90244453 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 5 level of Phosphatidylcholine (O-16:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045115 GCST90244454 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylcholine (O-16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045116 GCST90244455 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:0_22:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:0_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045117 GCST90244456 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_16:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:1_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045118 GCST90244457 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_18:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:1_18:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045119 GCST90244458 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-16:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045120 GCST90244459 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045121 GCST90244460 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-16:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045122 GCST90244461 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:1_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (O-16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045123 GCST90244462 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-16:2_18:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90244463 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-17:0_15:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-17:0_15:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045124 GCST90244464 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-17:0_17:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of phosphatidylcholine http://purl.obolibrary.org/obo/OBA_2040179 GCST90244465 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90244341 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90244342 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90244343 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 50:5 measurement http://www.ebi.ac.uk/efo/EFO_0010412 GCST90244344 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:1) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90244345 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90244346 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Triacylglycerol (51:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045163 GCST90244347 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Triacylglycerol (51:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045164 GCST90244348 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90244349 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90244350 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90244351 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 triacylglycerol 52:5 measurement http://www.ebi.ac.uk/efo/EFO_0010417 GCST90244352 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:6) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 0 triacylglycerol 52:6 measurement http://www.ebi.ac.uk/efo/EFO_0010418 GCST90244353 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (53:2) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90244354 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (53:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 level of Triacylglycerol (53:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045165 GCST90244355 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (53:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 level of Triacylglycerol (53:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045166 GCST90244356 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90244357 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 2 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90244358 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90244359 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:6) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90244360 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:7) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 54:7 measurement http://www.ebi.ac.uk/efo/EFO_0010425 GCST90244361 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:3) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 3 triacylglycerol 56:3 measurement http://www.ebi.ac.uk/efo/EFO_0010430 GCST90244362 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:4) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 56:4 measurement http://www.ebi.ac.uk/efo/EFO_0010431 GCST90244363 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:5) levels 2,624 European ancestry men NA Illumina [NR] (imputed) 1 triacylglycerol 56:5 measurement http://www.ebi.ac.uk/efo/EFO_0010432 GCST90244364 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol 56:6 levels 2,624 European ancestry men NA Illumina [NR] (imputed) 4 level of triacylglycerol (56:6) in blood serum http://purl.obolibrary.org/obo/OBA_2020007 GCST90244365 Genome-wide genotyping array 2023-04-25 36543923 Sherva R 2022-12-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36543923 African ancestry GWAS of dementia in a large military cohort identifies significant risk loci. Alzheimer's disease or related dementias (adjusted for APOE E4 dosage) 4,012 African American cases, 18,435 African American controls NA NR [16589632] (imputed) 7 Alzheimer disease, dementia http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/MONDO_0001627 GCST90267625 Genome-wide genotyping array 2023-04-25 36543923 Sherva R 2022-12-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36543923 African ancestry GWAS of dementia in a large military cohort identifies significant risk loci. Alzheimer's disease, proxy Alzheimer's disease or related dementias 6,796 African American cases, 4,385 African American maternal cases, 2,256 African American paternal cases, 69,627 African American controls NA NR [16589632] (imputed) 29 Alzheimer disease, dementia, family history of Alzheimer’s disease http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/MONDO_0001627, http://www.ebi.ac.uk/efo/EFO_0009268 GCST90267627 Genome-wide genotyping array 2023-04-25 36543923 Sherva R 2022-12-22 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36543923 African ancestry GWAS of dementia in a large military cohort identifies significant risk loci. Alzheimer's disease, proxy Alzheimer's disease or related dementias (adjusted for APOE E4 dosage) 6,796 African American cases, 4,385 African American maternal cases, 2,256 African American paternal cases, 69,627 African American controls NA NR [16589632] (imputed) 7 Alzheimer disease, dementia, family history of Alzheimer’s disease http://purl.obolibrary.org/obo/MONDO_0004975, http://purl.obolibrary.org/obo/MONDO_0001627, http://www.ebi.ac.uk/efo/EFO_0009268 GCST90267628 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (16:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylinositol (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045153 GCST90244491 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (16:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylinositol (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045154 GCST90244492 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 11 level of Phosphatidylinositol (18:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045155 GCST90244493 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 12 level of Phosphatidylinositol (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045156 GCST90244494 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 8 level of Phosphatidylinositol (18:0_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045157 GCST90244495 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 10 level of Phosphatidylinositol (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045158 GCST90244496 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:1_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 5 level of Phosphatidylinositol (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045159 GCST90244497 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylinositol (18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045160 GCST90244498 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (18:1_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylinositol (18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045161 GCST90244499 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d32:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 11 level of Sphingomyelin (d32:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045173 GCST90244500 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d34:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 9 level of Sphingomyelin (d34:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045176 GCST90244501 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d34:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 15 level of Sphingomyelin (d34:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045175 GCST90244502 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d34:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Sphingomyelin (d34:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045174 GCST90244503 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d36:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Sphingomyelin (d36:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045178 GCST90244504 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d36:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Sphingomyelin (d36:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045177 GCST90244505 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d38:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 26 level of Sphingomyelin (d38:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045180 GCST90244506 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d38:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 13 level of Sphingomyelin (d38:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045179 GCST90244507 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d40:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 30 level of Sphingomyelin (d40:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045182 GCST90244508 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d40:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 14 level of Sphingomyelin (d40:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045181 GCST90244509 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Sphingomyelin (d42:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 17 level of Sphingomyelin (d42:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045183 GCST90244510 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (46:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 triacylglycerol 46:1 measurement http://www.ebi.ac.uk/efo/EFO_0010401 GCST90244511 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (46:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 triacylglycerol 46:2 measurement http://www.ebi.ac.uk/efo/EFO_0010402 GCST90244512 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90244513 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90244514 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90244515 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:0_14:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-18:0_14:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045125 GCST90244466 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:0_16:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylcholine (O-18:0_16:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045126 GCST90244467 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylcholine (O-18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045127 GCST90244468 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_16:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:1_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045128 GCST90244469 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045129 GCST90244470 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_20:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:1_20:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045130 GCST90244471 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:1_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Phosphatidylcholine (O-18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045131 GCST90244472 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_16:0) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:2_16:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045132 GCST90244473 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:2_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045133 GCST90244474 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045134 GCST90244475 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylcholine (O-18:2_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylcholine (O-18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045135 GCST90244476 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (16:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 15 level of Phosphatidylethanolamine (16:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045136 GCST90244477 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (16:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 13 level of Phosphatidylethanolamine (16:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045137 GCST90244478 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:0_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 17 level of Phosphatidylethanolamine (18:0_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045139 GCST90244479 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:0_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 12 level of Phosphatidylethanolamine (18:0_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045140 GCST90244480 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (18:1_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 9 level of Phosphatidylethanolamine (18:1_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045142 GCST90244481 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-16:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-16:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045144 GCST90244482 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-16:1_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylethanolamine (O-16:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045145 GCST90244483 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-16:1_22:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 level of Phosphatidylethanolamine (O-16:1_22:5) in blood serum http://purl.obolibrary.org/obo/OBA_2045146 GCST90244484 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:1_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 level of Phosphatidylethanolamine (O-18:1_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045147 GCST90244485 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:1_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 5 level of Phosphatidylethanolamine (O-18:1_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045148 GCST90244486 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:2_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:2_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045149 GCST90244487 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:2_18:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:2_18:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045150 GCST90244488 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylethanolamine (O-18:2_20:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Phosphatidylethanolamine (O-18:2_20:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045151 GCST90244489 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Phosphatidylinositol (16:0_18:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Phosphatidylinositol (16:0_18:1) in blood serum http://purl.obolibrary.org/obo/OBA_2045152 GCST90244490 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (48:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90244516 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (49:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90244517 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (49:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 level of Triacylglycerol (49:2) in blood serum http://purl.obolibrary.org/obo/OBA_2045162 GCST90244518 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90244519 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90244520 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90244521 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90244522 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (50:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 triacylglycerol 50:5 measurement http://www.ebi.ac.uk/efo/EFO_0010412 GCST90244523 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:1) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90244524 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 triacylglycerol 51:2 measurement http://www.ebi.ac.uk/efo/EFO_0021483 GCST90244525 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Triacylglycerol (51:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045163 GCST90244526 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (51:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 1 level of Triacylglycerol (51:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045164 GCST90244527 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90244528 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 7 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90244529 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90244530 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 triacylglycerol 52:5 measurement http://www.ebi.ac.uk/efo/EFO_0010417 GCST90244531 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (52:6) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 triacylglycerol 52:6 measurement http://www.ebi.ac.uk/efo/EFO_0010418 GCST90244532 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (53:2) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90244533 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (53:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 level of Triacylglycerol (53:3) in blood serum http://purl.obolibrary.org/obo/OBA_2045165 GCST90244534 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (53:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 level of Triacylglycerol (53:4) in blood serum http://purl.obolibrary.org/obo/OBA_2045166 GCST90244535 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 9 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90244536 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 7 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90244537 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 6 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90244538 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:6) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90244539 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (54:7) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 triacylglycerol 54:7 measurement http://www.ebi.ac.uk/efo/EFO_0010425 GCST90244540 Genome-wide genotyping array 2023-08-30 37539667 Park HA 2023-08-04 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/37539667 Genome-wide study of genetic polymorphisms predictive for outcome from first-line oxaliplatin-based chemotherapy in colorectal cancer patients. Overall survival in stage III colon cancer (oxaliplatin-based chemotherapy vs chemotherapy without oxaliplatin) 3,231 European ancestry individuals treated with oxaliplatin, 416 European ancestry individuals treated with other treatment NA Illumina [4666455] (imputed) 1 colon carcinoma, overall survival, trait in response to oxaliplatin http://www.ebi.ac.uk/efo/EFO_1001950, http://www.ebi.ac.uk/efo/EFO_0000638, http://purl.obolibrary.org/obo/OBA_2050333 GCST90267408 Genome-wide genotyping array 2023-08-30 37539667 Park HA 2023-08-04 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/37539667 Genome-wide study of genetic polymorphisms predictive for outcome from first-line oxaliplatin-based chemotherapy in colorectal cancer patients. Progression free survival in stage III colon cancer (oxaliplatin-based chemotherapy vs chemotherapy without oxaliplatin) 3,231 European ancestry individuals treated with oxaliplatin, 416 European ancestry individuals treated with other treatment NA Illumina [4667061] (imputed) 1 progression free survival, colon carcinoma, trait in response to oxaliplatin http://www.ebi.ac.uk/efo/EFO_0004920, http://www.ebi.ac.uk/efo/EFO_1001950, http://purl.obolibrary.org/obo/OBA_2050333 GCST90267409 Genome-wide genotyping array 2023-08-30 37539667 Park HA 2023-08-04 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/37539667 Genome-wide study of genetic polymorphisms predictive for outcome from first-line oxaliplatin-based chemotherapy in colorectal cancer patients. Overall survival in metastatic colorectal cancer (oxaliplatin-based chemotherapy vs chemotherapy without oxaliplatin) 547 European ancestry individuals treated with oxaliplatin, 395 European ancestry individuals treated with other treatment 389 European ancestry individuals treated with oxaliplatin, 100 European ancestry individuals treated with other treatment Illumina [4661209] (imputed) 0 overall survival, colorectal carcinoma, trait in response to oxaliplatin http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1001951, http://purl.obolibrary.org/obo/OBA_2050333 GCST90267410 Genome-wide genotyping array 2023-08-30 37539667 Park HA 2023-08-04 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/37539667 Genome-wide study of genetic polymorphisms predictive for outcome from first-line oxaliplatin-based chemotherapy in colorectal cancer patients. Progression free survival in metastatic colorectal cancer (oxaliplatin-based chemotherapy vs chemotherapy without oxaliplatin) 547 European ancestry individuals treated with oxaliplatin, 395 European ancestry individuals treated with other treatment 389 European ancestry individuals treated with oxaliplatin, 100 European ancestry individuals treated with other treatment Illumina [4661211] (imputed) 0 overall survival, colorectal carcinoma, trait in response to oxaliplatin http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1001951, http://purl.obolibrary.org/obo/OBA_2050333 GCST90267411 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:3) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 triacylglycerol 56:3 measurement http://www.ebi.ac.uk/efo/EFO_0010430 GCST90244541 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:4) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 3 triacylglycerol 56:4 measurement http://www.ebi.ac.uk/efo/EFO_0010431 GCST90244542 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:5) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 triacylglycerol 56:5 measurement http://www.ebi.ac.uk/efo/EFO_0010432 GCST90244543 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol 56:6 levels 4,642 European ancestry women NA Illumina [NR] (imputed) 14 level of triacylglycerol (56:6) in blood serum http://purl.obolibrary.org/obo/OBA_2020007 GCST90244544 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:7) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 7 triacylglycerol 56:7 measurement http://www.ebi.ac.uk/efo/EFO_0010434 GCST90244545 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (56:8) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 5 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90244546 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (58:7) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 4 triacylglycerol 58:7 measurement http://www.ebi.ac.uk/efo/EFO_0010441 GCST90244547 Genome-wide genotyping array 2023-08-25 36193934 Tabassum R 2022-10-04 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36193934 Lipidome- and Genome-Wide Study to Understand Sex Differences in Circulatory Lipids. Triacylglycerol (58:8) levels 4,642 European ancestry women NA Illumina [NR] (imputed) 2 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90244548 Genome-wide genotyping array 2023-07-07 36970523 Herrera-Rivero M 2023-03-08 Front Neurol www.ncbi.nlm.nih.gov/pubmed/36970523 Evidence of polygenic regulation of the physiological presence of neurofilament light chain in human serum. Serum neurofilament light levels 1,899 European ancestry individuals NA Illumina [5597244] (imputed) 13 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST90271744 Genome-wide genotyping array 2023-07-07 36970523 Herrera-Rivero M 2023-03-08 Front Neurol www.ncbi.nlm.nih.gov/pubmed/36970523 Evidence of polygenic regulation of the physiological presence of neurofilament light chain in human serum. Serum neurofilament light levels 2,186 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 7 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST90271745 Genome-wide genotyping array 2023-06-27 36809439 Soremekun C 2023-02-21 PLoS One www.ncbi.nlm.nih.gov/pubmed/36809439 Multivariate GWAS analysis reveals loci associated with liver functions in continental African populations. Liver biomarker levels 6,407 Ugandan ancestry individuals 2,598 South African Zulu ancestry individuals Illumina [NR] 0 liver disease biomarker http://www.ebi.ac.uk/efo/EFO_0006845 GCST90271579 Genome-wide genotyping array, Genome-wide sequencing 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Total testosterone levels 176,212 British ancestry men NA Affymetrix [17239132] (imputed) 200 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90239819 Genome-wide genotyping array 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Total testosterone levels 174,850 British ancestry women NA Affymetrix [17239132] (imputed) 107 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90239820 Genome-wide genotyping array 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Sex hormone-binding globulin levels 163,363 British ancestry men NA Affymetrix [17239132] (imputed) 263 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90239821 Genome-wide genotyping array 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Sex hormone-binding globulin levels 188,443 British ancestry women NA Affymetrix [17239132] (imputed) 248 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90239822 Genome-wide genotyping array 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Free androgen index 162,068 British ancestry men NA Affymetrix [17239132] (imputed) 156 free androgen index http://www.ebi.ac.uk/efo/EFO_0007005 GCST90239823 Genome-wide genotyping array 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Free androgen index 158,208 British ancestry women NA Affymetrix [17239132] (imputed) 168 free androgen index http://www.ebi.ac.uk/efo/EFO_0007005 GCST90239824 Genome-wide genotyping array 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Free testosterone levels 161,887 British ancestry men NA Affymetrix [17239132] (imputed) 107 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90239825 Genome-wide genotyping array 2023-08-31 36653534 Leinonen JT 2023-01-18 Commun Med (Lond) www.ncbi.nlm.nih.gov/pubmed/36653534 Genetic analyses implicate complex links between adult testosterone levels and health and disease. Free testosterone levels 158,089 British ancestry women NA Affymetrix [17239132] (imputed) 134 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90239826 Genome-wide genotyping array 2023-08-10 36974753 Dong X 2023-03-28 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36974753 Unprocessed Red Meat and Processed Meat Consumption, Plasma Metabolome, and Risk of Ischemic Heart Disease: A Prospective Cohort Study of UK Biobank. Red meat related metabolomic signature 87,678 European ancestry individuals, 4,568 individuals NA NR [NR] (imputed) 45 metabolite measurement, diet measurement http://www.ebi.ac.uk/efo/EFO_0004725, http://www.ebi.ac.uk/efo/EFO_0008111 GCST90277236 Genome-wide genotyping array 2023-08-10 36974753 Dong X 2023-03-28 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36974753 Unprocessed Red Meat and Processed Meat Consumption, Plasma Metabolome, and Risk of Ischemic Heart Disease: A Prospective Cohort Study of UK Biobank. Processed meat related metabolomic signature 87,678 European ancestry individuals, 4,568 individuals NA NR [NR] (imputed) 4 metabolite measurement, diet measurement http://www.ebi.ac.uk/efo/EFO_0004725, http://www.ebi.ac.uk/efo/EFO_0008111 GCST90277237 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in LDL (UKB data field 23425) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 total lipids in LDL measurement http://www.ebi.ac.uk/efo/EFO_0022308 GCST90269522 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in HDL (UKB data field 23426) 88,329 European ancestry individuals NA NR [16366144] (imputed) 51 total lipids in HDL measurement http://www.ebi.ac.uk/efo/EFO_0022307 GCST90269523 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total concentration of lipoprotein particles (UKB data field 23427) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004732 GCST90269524 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of VLDL particles (UKB data field 23428) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90269525 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of LDL particles (UKB data field 23429) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90269526 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of HDL particles (UKB data field 23430) 88,329 European ancestry individuals NA NR [16366144] (imputed) 40 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90269527 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Average diameter for VLDL particles (UKB data field 23431) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90269528 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Average diameter for LDL particles (UKB data field 23432) 88,329 European ancestry individuals NA NR [16366144] (imputed) 20 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90269529 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Average diameter for HDL particles (UKB data field 23433) 88,329 European ancestry individuals NA NR [16366144] (imputed) 51 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90269530 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phosphoglycerides levels (UKB data field 23434) 88,268 European ancestry individuals NA NR [16366159] (imputed) 39 phosphoglycerides measurement http://www.ebi.ac.uk/efo/EFO_0022291 GCST90269531 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to phosphoglycerides ratio (UKB data field 23435) 88,268 European ancestry individuals NA NR [16366159] (imputed) 49 triglycerides to phosphoglycerides ratio http://www.ebi.ac.uk/efo/EFO_0022327 GCST90269532 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total cholines levels (UKB data field 23436) 88,268 European ancestry individuals NA NR [16366159] (imputed) 39 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90269533 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phosphatidylcholines levels (UKB data field 23437) 88,268 European ancestry individuals NA NR [16366159] (imputed) 40 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90269534 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Sphingomyelins levels (UKB data field 23438) 88,268 European ancestry individuals NA NR [16366159] (imputed) 38 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90269535 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Apolipoprotein B levels (UKB data field 23439) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90269536 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Apolipoprotein A1 levels (UKB data field 23440) 88,329 European ancestry individuals NA NR [16366144] (imputed) 48 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90269537 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Apolipoprotein B to apolipoprotein A1 ratio (UKB data field 23441) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 apolipoprotein B to apolipoprotein A1 ratio http://www.ebi.ac.uk/efo/EFO_0021897 GCST90269538 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total fatty acids levels (UKB data field 23442) 88,268 European ancestry individuals NA NR [16366159] (imputed) 38 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90269539 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Degree of unsaturation (UKB data field 23443) 88,268 European ancestry individuals NA NR [16366159] (imputed) 27 degree of unsaturation measurement http://www.ebi.ac.uk/efo/EFO_0022261 GCST90269540 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Omega-3 fatty acids levels (UKB data field 23444) 88,268 European ancestry individuals NA NR [16366159] (imputed) 27 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90269541 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Omega-6 fatty acids levels (UKB data field 23445) 88,268 European ancestry individuals NA NR [16366159] (imputed) 35 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90269542 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Polyunsaturated fatty acids levels (UKB data field 23446) 88,268 European ancestry individuals NA NR [16366159] (imputed) 41 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST90269543 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Monounsaturated fatty acids levels (UKB data field 23447) 88,268 European ancestry individuals NA NR [16366159] (imputed) 37 monounsaturated fatty acids; 16:1, 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0022187 GCST90269544 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Saturated fatty acids levels (UKB data field 23448) 88,268 European ancestry individuals NA NR [16366159] (imputed) 31 saturated fatty acids measurement http://www.ebi.ac.uk/efo/EFO_0022304 GCST90269545 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Linoleic acid levels (UKB data field 23449) 88,268 European ancestry individuals NA NR [16366159] (imputed) 34 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90269546 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total cholesterol levels (UKB data field 23400) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90269497 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total cholesterol minus HDL-C levels (UKB data field 23401) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90269498 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Remnant cholesterol (non-HDL, non-LDL -cholesterol) levels (UKB data field 23402) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 remnant cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010815 GCST90269499 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. VLDL cholesterol levels (UKB data field 23403) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90269500 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Clinical LDL cholesterol levels (UKB data field 23404) 88,329 European ancestry individuals NA NR [16366144] (imputed) 32 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90269501 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. LDL cholesterol levels (UKB data field 23405) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90269502 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. HDL cholesterol levels (UKB data field 23406) 88,329 European ancestry individuals NA NR [16366144] (imputed) 54 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90269503 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total triglycerides levels (UKB data field 23407) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90269504 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in VLDL (UKB data field 23408) 88,329 European ancestry individuals NA NR [16366144] (imputed) 45 triglycerides in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022326 GCST90269505 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in LDL (UKB data field 23409) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 triglycerides in LDL measurement http://www.ebi.ac.uk/efo/EFO_0022320 GCST90269506 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in HDL (UKB data field 23410) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 triglycerides in HDL measurement http://www.ebi.ac.uk/efo/EFO_0022317 GCST90269507 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total phospholipids in lipoprotein particles (UKB data field 23411) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 total phospholipids in lipoprotein particles measurement http://www.ebi.ac.uk/efo/EFO_0022315 GCST90269508 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in VLDL (UKB data field 23412) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90269509 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in LDL (UKB data field 23413) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 phospholipids in LDL measurement http://www.ebi.ac.uk/efo/EFO_0022294 GCST90269510 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in HDL (UKB data field 23414) 88,329 European ancestry individuals NA NR [16366144] (imputed) 48 phospholipids in HDL measurement http://www.ebi.ac.uk/efo/EFO_0022293 GCST90269511 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total esterified cholesterol levels (UKB data field 23415) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90269512 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in VLDL (UKB data field 23416) 88,329 European ancestry individuals NA NR [16366144] (imputed) 37 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269513 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in LDL (UKB data field 23417) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269514 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in HDL (UKB data field 23418) 88,329 European ancestry individuals NA NR [16366144] (imputed) 55 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269515 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total free cholesterol levels (UKB data field 23419) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90269516 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in VLDL (UKB data field 23420) 88,329 European ancestry individuals NA NR [16366144] (imputed) 40 free cholesterol in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022276 GCST90269517 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in LDL (UKB data field 23421) 88,329 European ancestry individuals NA NR [16366144] (imputed) 30 free cholesterol in LDL measurement http://www.ebi.ac.uk/efo/EFO_0022266 GCST90269518 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in HDL (UKB data field 23422) 88,329 European ancestry individuals NA NR [16366144] (imputed) 50 free cholesterol in HDL measurement http://www.ebi.ac.uk/efo/EFO_0022264 GCST90269519 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in lipoprotein particles (UKB data field 23423) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 total lipids in lipoprotein particles measurement http://www.ebi.ac.uk/efo/EFO_0022309 GCST90269520 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in VLDL (UKB data field 23424) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 total lipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022314 GCST90269521 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Docosahexaenoic acid levels (UKB data field 23450) 88,268 European ancestry individuals NA NR [16366159] (imputed) 30 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90269547 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Omega-3 fatty acids to total fatty acids percentage (UKB data field 23451) 88,268 European ancestry individuals NA NR [16366159] (imputed) 25 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90269548 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Omega-6 fatty acids to total fatty acids percentage (UKB data field 23452) 88,268 European ancestry individuals NA NR [16366159] (imputed) 33 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90269549 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Polyunsaturated fatty acids to total fatty acids percentage (UKB data field 23453) 88,268 European ancestry individuals NA NR [16366159] (imputed) 32 polyunsaturated fatty acids to total fatty acids percentage http://www.ebi.ac.uk/efo/EFO_0022303 GCST90269550 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Monounsaturated fatty acids to total fatty acids percentage (UKB data field 23454) 88,268 European ancestry individuals NA NR [16366159] (imputed) 36 monounsaturated fatty acids; 16:1, 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0022187 GCST90269551 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Saturated fatty acids to total fatty acids percentage (UKB data field 23455) 88,268 European ancestry individuals NA NR [16366159] (imputed) 15 saturated fatty acids to total fatty acids percentage http://www.ebi.ac.uk/efo/EFO_0022305 GCST90269552 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Linoleic acid to total fatty acids percentage (UKB data field 23456) 88,268 European ancestry individuals NA NR [16366159] (imputed) 18 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90269553 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Docosahexaenoic acid to total fatty acids percentage (UKB data field 23457) 88,268 European ancestry individuals NA NR [16366159] (imputed) 17 docosahexaenoic acid to total fatty acids percentage http://www.ebi.ac.uk/efo/EFO_0022262 GCST90269554 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Polyunsaturated fatty acids to monounsaturated fatty acids ratio (UKB data field 23458) 88,268 European ancestry individuals NA NR [16366159] (imputed) 34 polyunsaturated fatty acids to monounsaturated fatty acids ratio http://www.ebi.ac.uk/efo/EFO_0022302 GCST90269555 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Omega-6 fatty acids to omega-3 fatty acids ratio (UKB data field 23459) 88,268 European ancestry individuals NA NR [16366159] (imputed) 23 omega-6:omega-3 polyunsaturated fatty acid ratio http://www.ebi.ac.uk/efo/EFO_0010732 GCST90269556 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Alanine levels (UKB data field 23460) 88,325 European ancestry individuals NA NR [16366119] (imputed) 27 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90269557 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Glutamine levels (UKB data field 23461) 88,070 European ancestry individuals NA NR [16366084] (imputed) 19 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90269558 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Glycine levels (UKB data field 23462) 88,258 European ancestry individuals NA NR [16366042] (imputed) 24 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90269559 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Histidine levels (UKB data field 23463) 88,197 European ancestry individuals NA NR [16365980] (imputed) 11 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90269560 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total concentration of branched-chain amino acids (leucine + isoleucine + valine) (UKB data field 23464) 88,303 European ancestry individuals NA NR [16366192] (imputed) 11 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90269561 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Isoleucine levels (UKB data field 23465) 88,326 European ancestry individuals NA NR [16366115] (imputed) 6 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90269562 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Leucine levels (UKB data field 23466) 88,326 European ancestry individuals NA NR [16366115] (imputed) 9 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90269563 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Valine levels (UKB data field 23467) 88,303 European ancestry individuals NA NR [16366192] (imputed) 13 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90269564 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phenylalanine levels (UKB data field 23468) 88,296 European ancestry individuals NA NR [16366185] (imputed) 4 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90269565 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Tyrosine levels (UKB data field 23469) 88,207 European ancestry individuals NA NR [16365997] (imputed) 19 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90269566 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Glucose levels (UKB data field 23470) 88,174 European ancestry individuals NA NR [16366051] (imputed) 10 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90269567 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Lactate levels (UKB data field 23471) 88,119 European ancestry individuals NA NR [16365921] (imputed) 6 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90269568 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Pyruvate levels (UKB data field 23472) 88,069 European ancestry individuals NA NR [16366090] (imputed) 13 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90269569 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Citrate levels (UKB data field 23473) 88,318 European ancestry individuals NA NR [16366101] (imputed) 21 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90269570 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. 3-hydroxybutyrate levels (UKB data field 23474) 87,151 European ancestry individuals NA NR [16366252] (imputed) 9 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90269571 Genome-wide genotyping array 2023-04-27 36620623 Ahn J 2022-12-22 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/36620623 Genome-wide association study for vascular aging highlights pathways shared with cardiovascular traits in Koreans. Vascular endothelial function 97 Korean ancestry individuals NA Illumina [3084757] (imputed) 78 vascular endothelial function measurement http://www.ebi.ac.uk/efo/EFO_0803369 GCST90255363 Genome-wide genotyping array 2023-04-27 36620623 Ahn J 2022-12-22 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/36620623 Genome-wide association study for vascular aging highlights pathways shared with cardiovascular traits in Koreans. Vascular endothelial function 97 Korean ancestry individuals NA Illumina [177236] 26 vascular endothelial function measurement http://www.ebi.ac.uk/efo/EFO_0803369 GCST90255362 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Acetate levels (UKB data field 23475) 88,306 European ancestry individuals NA NR [16366137] (imputed) 5 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90269572 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Acetoacetate levels (UKB data field 23476) 88,326 European ancestry individuals NA NR [16366115] (imputed) 4 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90269573 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Acetone levels (UKB data field 23477) 88,326 European ancestry individuals NA NR [16366115] (imputed) 5 acetone measurement http://www.ebi.ac.uk/efo/EFO_0010989 GCST90269574 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Creatinine levels (UKB data field 23478) 84,405 European ancestry individuals NA NR [16363651] (imputed) 32 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90269575 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Albumin levels (UKB data field 23479) 88,315 European ancestry individuals NA NR [16366183] (imputed) 15 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90269576 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Glycoprotein acetyls levels (UKB data field 23480) 88,329 European ancestry individuals NA NR [16366144] (imputed) 27 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90269577 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of chylomicrons and extremely large VLDL particles (UKB data field 23481) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 concentration of chylomicrons and extremely large VLDL particles measurement http://www.ebi.ac.uk/efo/EFO_0022260 GCST90269578 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in chylomicrons and extremely large VLDL (UKB data field 23482) 88,329 European ancestry individuals NA NR [16366144] (imputed) 45 total lipids in chylomicrons and extremely large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022306 GCST90269579 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in chylomicrons and extremely large VLDL (UKB data field 23483) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 phospholipids in chylomicrons and extremely large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022292 GCST90269580 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in chylomicrons and extremely large VLDL (UKB data field 23484) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 cholesterol in chylomicrons and extremely large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0021898 GCST90269581 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in chylomicrons and extremely large VLDL (UKB data field 23485) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269582 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in chylomicrons and extremely large VLDL (UKB data field 23486) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 free cholesterol in chylomicrons and extremely large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022263 GCST90269583 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in chylomicrons and extremely large VLDL (UKB data field 23487) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 triglycerides in chylomicrons and extremely large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022316 GCST90269584 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of very large VLDL particles (UKB data field 23488) 88,329 European ancestry individuals NA NR [16366144] (imputed) 47 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90269585 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in very large VLDL (UKB data field 23489) 88,329 European ancestry individuals NA NR [16366144] (imputed) 47 total lipids in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022313 GCST90269586 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in very large VLDL (UKB data field 23490) 88,329 European ancestry individuals NA NR [16366144] (imputed) 47 phospholipids in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022299 GCST90269587 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in very large VLDL (UKB data field 23491) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 cholesterol in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022230 GCST90269588 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in very large VLDL (UKB data field 23492) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269589 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in very large VLDL (UKB data field 23493) 88,329 European ancestry individuals NA NR [16366144] (imputed) 46 free cholesterol in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022274 GCST90269590 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in very large VLDL (UKB data field 23494) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 triglycerides in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022325 GCST90269591 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of large VLDL particles (UKB data field 23495) 88,329 European ancestry individuals NA NR [16366144] (imputed) 48 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90269592 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in large VLDL (UKB data field 23496) 88,329 European ancestry individuals NA NR [16366144] (imputed) 49 total lipids in large VLDL http://www.ebi.ac.uk/efo/EFO_0022175 GCST90269593 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in large VLDL (UKB data field 23497) 88,329 European ancestry individuals NA NR [16366144] (imputed) 49 phospholipids in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022169 GCST90269594 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in large VLDL (UKB data field 23498) 88,329 European ancestry individuals NA NR [16366144] (imputed) 46 cholesterol in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0021902 GCST90269595 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in large VLDL (UKB data field 23499) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269596 Genome-wide genotyping array 2023-08-09 37038246 Chen HY 2023-04-11 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/37038246 Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study. Aortic stenosis 13,765 European ancestry cases, 640,102 European ancestry controls 7,111 European ancestry cases, 83,717 European ancestry controls Affymetrix, Illumina [11591806] (imputed) 18 aortic stenosis http://www.ebi.ac.uk/efo/EFO_0000266 GCST90276156 Genome-wide genotyping array 2023-07-20 36935420 Flanigan KM 2023-03-20 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36935420 A genome-wide association analysis of loss of ambulation in dystrophinopathy patients suggests multiple candidate modifiers of disease severity. Loss of ambulation in Duchenne muscular dystrophy 419 individuals NA NR [NR] 0 Duchenne muscular dystrophy, Loss of ambulation http://purl.obolibrary.org/obo/MONDO_0010679, http://purl.obolibrary.org/obo/HP_0002505 GCST90274731 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in large VLDL (UKB data field 23500) 88,329 European ancestry individuals NA NR [16366144] (imputed) 50 free cholesterol in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022265 GCST90269597 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in large VLDL (UKB data field 23501) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 triglycerides in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022178 GCST90269598 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of medium VLDL particles (UKB data field 23502) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90269599 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in medium VLDL (UKB data field 23503) 88,329 European ancestry individuals NA NR [16366144] (imputed) 37 total lipids in medium VLDL http://www.ebi.ac.uk/efo/EFO_0022153 GCST90269600 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in medium VLDL (UKB data field 23504) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 phospholipids in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022154 GCST90269601 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in medium VLDL (UKB data field 23505) 88,329 European ancestry individuals NA NR [16366144] (imputed) 37 cholesterol in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022225 GCST90269602 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in medium VLDL (UKB data field 23506) 88,329 European ancestry individuals NA NR [16366144] (imputed) 33 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269603 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in medium VLDL (UKB data field 23507) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 free cholesterol in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022269 GCST90269604 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in medium VLDL (UKB data field 23508) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 triglycerides in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022155 GCST90269605 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of small VLDL particles (UKB data field 23509) 88,329 European ancestry individuals NA NR [16366144] (imputed) 45 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90269606 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in small VLDL (UKB data field 23510) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 total lipids in small VLDL http://www.ebi.ac.uk/efo/EFO_0022148 GCST90269607 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in small VLDL (UKB data field 23511) 88,329 European ancestry individuals NA NR [16366144] (imputed) 45 phospholipids in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022146 GCST90269608 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in small VLDL (UKB data field 23512) 88,329 European ancestry individuals NA NR [16366144] (imputed) 40 cholesterol in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022228 GCST90269609 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in small VLDL (UKB data field 23513) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269610 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in small VLDL (UKB data field 23514) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 free cholesterol in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022272 GCST90269611 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in small VLDL (UKB data field 23515) 88,329 European ancestry individuals NA NR [16366144] (imputed) 46 triglycerides in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022145 GCST90269612 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of very small VLDL particles (UKB data field 23516) 88,329 European ancestry individuals NA NR [16366144] (imputed) 37 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90269613 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in very small VLDL (UKB data field 23517) 88,329 European ancestry individuals NA NR [16366144] (imputed) 37 total lipids in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022156 GCST90269614 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in very small VLDL (UKB data field 23518) 88,329 European ancestry individuals NA NR [16366144] (imputed) 40 phospholipids in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022300 GCST90269615 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in very small VLDL (UKB data field 23519) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022231 GCST90269616 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in very small VLDL (UKB data field 23520) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269617 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in very small VLDL (UKB data field 23521) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 free cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022275 GCST90269618 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in very small VLDL (UKB data field 23522) 88,329 European ancestry individuals NA NR [16366144] (imputed) 48 triglycerides in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022144 GCST90269619 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of IDL particles (UKB data field 23523) 88,329 European ancestry individuals NA NR [16366144] (imputed) 32 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90269620 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in IDL (UKB data field 23524) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 total lipids in IDL http://www.ebi.ac.uk/efo/EFO_0022161 GCST90269621 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in IDL (UKB data field 23525) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 phospholipids in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022164 GCST90269622 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in IDL (UKB data field 23526) 88,329 European ancestry individuals NA NR [16366144] (imputed) 40 cholesterol in IDL measurement http://www.ebi.ac.uk/efo/EFO_0021899 GCST90269623 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in IDL (UKB data field 23527) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269624 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in IDL (UKB data field 23528) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 free cholesterol in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022181 GCST90269625 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in IDL (UKB data field 23529) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 triglycerides in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022149 GCST90269626 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of large LDL particles (UKB data field 23530) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 concentration of large LDL particles measurement http://www.ebi.ac.uk/efo/EFO_0022160 GCST90269627 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in large LDL (UKB data field 23531) 88,329 European ancestry individuals NA NR [16366144] (imputed) 37 total lipids in large LDL http://www.ebi.ac.uk/efo/EFO_0022163 GCST90269628 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in large LDL (UKB data field 23532) 88,329 European ancestry individuals NA NR [16366144] (imputed) 33 phospholipids in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022174 GCST90269629 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in large LDL (UKB data field 23533) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 cholesterol in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0021901 GCST90269630 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in large LDL (UKB data field 23534) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269631 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in large LDL (UKB data field 23535) 88,329 European ancestry individuals NA NR [16366144] (imputed) 32 free cholesterol in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022176 GCST90269632 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in large LDL (UKB data field 23536) 88,329 European ancestry individuals NA NR [16366144] (imputed) 34 triglycerides in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022319 GCST90269633 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of medium LDL particles (UKB data field 23537) 88,329 European ancestry individuals NA NR [16366144] (imputed) 34 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90269634 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in medium LDL (UKB data field 23538) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 total lipids in medium LDL http://www.ebi.ac.uk/efo/EFO_0022180 GCST90269635 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in medium LDL (UKB data field 23539) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 phospholipids in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022183 GCST90269636 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in medium LDL (UKB data field 23540) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 cholesterol in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022224 GCST90269637 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in medium LDL (UKB data field 23541) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269638 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in medium LDL (UKB data field 23542) 88,329 European ancestry individuals NA NR [16366144] (imputed) 29 free cholesterol in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022268 GCST90269639 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in medium LDL (UKB data field 23543) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 triglycerides in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022322 GCST90269640 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of small LDL particles (UKB data field 23544) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90269641 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in small LDL (UKB data field 23545) 88,329 European ancestry individuals NA NR [16366144] (imputed) 34 total lipids in small LDL http://www.ebi.ac.uk/efo/EFO_0022168 GCST90269642 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in small LDL (UKB data field 23546) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 phospholipids in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022297 GCST90269643 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in small LDL (UKB data field 23547) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 cholesterol in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022227 GCST90269644 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in small LDL (UKB data field 23548) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269645 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in small LDL (UKB data field 23549) 88,329 European ancestry individuals NA NR [16366144] (imputed) 33 free cholesterol in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022271 GCST90269646 Genome-wide genotyping array 2023-07-28 36989840 Sofer T 2023-03-27 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/36989840 Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sex. Obstructive sleep apnea 23,651 black cases, 84,817 black controls, 1,720 Asian ancestry cases, 6,361 Asian ancestry controls, 117,496 European ancestry cases, 635,463 European ancestry controls, 11,056 Hispanic or Latin American cases, 34,840 Hispanic or Latin American controls, 130 cases, 1,162 controls NA Affymetrix, Illumina [NR] (imputed) 31 obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0003918 GCST90274865 Genome-wide genotyping array 2023-07-28 36989840 Sofer T 2023-03-27 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/36989840 Genome-wide association study of obstructive sleep apnoea in the Million Veteran Program uncovers genetic heterogeneity by sex. Obstructive sleep apnea (BMI adjusted) up to 23,651 black cases, up to 84,817 black controls, up to 1,720 Asian ancestry cases, up to 6,361 Asian ancestry controls, up to 117,496 European ancestry cases, up to 635,463 European ancestry controls, up to 11,056 Hispanic or Latin American cases, up to 34,840 Hispanic or Latin American controls, up to 130 cases, up to 1,162 controls NA Affymetrix, Illumina [NR] (imputed) 12 obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0003918 GCST90274866 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in small VLDL percentage (UKB data field 23600) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 cholesterol to total lipids in small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022242 GCST90269697 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in small VLDL percentage (UKB data field 23601) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 cholesteryl esters to total lipids in small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022256 GCST90269698 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in small VLDL percentage (UKB data field 23602) 88,329 European ancestry individuals NA NR [16366144] (imputed) 49 free cholesterol to total lipids in small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022287 GCST90269699 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in small VLDL percentage (UKB data field 23603) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 triglycerides to total lipids in small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022338 GCST90269700 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in very small VLDL percentage (UKB data field 23604) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269701 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in very small VLDL percentage (UKB data field 23605) 88,329 European ancestry individuals NA NR [16366144] (imputed) 53 cholesterol to total lipids in very small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022245 GCST90269702 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in very small VLDL percentage (UKB data field 23606) 88,329 European ancestry individuals NA NR [16366144] (imputed) 56 cholesteryl esters to total lipids in very small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022259 GCST90269703 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in very small VLDL percentage (UKB data field 23607) 88,329 European ancestry individuals NA NR [16366144] (imputed) 32 free cholesterol to total lipids in very small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022290 GCST90269704 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in very small VLDL percentage (UKB data field 23608) 88,329 European ancestry individuals NA NR [16366144] (imputed) 52 triglycerides to total lipids in very small VLDL percentage http://www.ebi.ac.uk/efo/EFO_0022341 GCST90269705 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in IDL percentage (UKB data field 23609) 88,329 European ancestry individuals NA NR [16366144] (imputed) 29 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269706 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in IDL percentage (UKB data field 23610) 88,329 European ancestry individuals NA NR [16366144] (imputed) 46 cholesterol to total lipids in IDL percentage http://www.ebi.ac.uk/efo/EFO_0022233 GCST90269707 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in IDL percentage (UKB data field 23611) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 cholesteryl esters to total lipids in IDL percentage http://www.ebi.ac.uk/efo/EFO_0022247 GCST90269708 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in IDL percentage (UKB data field 23612) 88,329 European ancestry individuals NA NR [16366144] (imputed) 25 free cholesterol to total lipids in IDL percentage http://www.ebi.ac.uk/efo/EFO_0022278 GCST90269709 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in IDL percentage (UKB data field 23613) 88,329 European ancestry individuals NA NR [16366144] (imputed) 49 triglycerides to total lipids in IDL percentage http://www.ebi.ac.uk/efo/EFO_0022329 GCST90269710 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in large LDL percentage (UKB data field 23614) 88,329 European ancestry individuals NA NR [16366144] (imputed) 27 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269711 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in large LDL percentage (UKB data field 23615) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 cholesterol to total lipids in large LDL percentage http://www.ebi.ac.uk/efo/EFO_0022235 GCST90269712 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in large LDL percentage (UKB data field 23616) 88,329 European ancestry individuals NA NR [16366144] (imputed) 24 cholesteryl esters to total lipids in large LDL percentage http://www.ebi.ac.uk/efo/EFO_0022249 GCST90269713 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in large LDL percentage (UKB data field 23617) 88,329 European ancestry individuals NA NR [16366144] (imputed) 54 free cholesterol to total lipids in large LDL percentage http://www.ebi.ac.uk/efo/EFO_0022280 GCST90269714 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in large LDL percentage (UKB data field 23618) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 triglycerides to total lipids in large LDL percentage http://www.ebi.ac.uk/efo/EFO_0022331 GCST90269715 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in medium LDL percentage (UKB data field 23619) 88,329 European ancestry individuals NA NR [16366144] (imputed) 22 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269716 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in medium LDL percentage (UKB data field 23620) 88,329 European ancestry individuals NA NR [16366144] (imputed) 20 cholesterol to total lipids in medium LDL percentage http://www.ebi.ac.uk/efo/EFO_0022238 GCST90269717 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in medium LDL percentage (UKB data field 23621) 88,329 European ancestry individuals NA NR [16366144] (imputed) 27 cholesteryl esters to total lipids in medium LDL percentage http://www.ebi.ac.uk/efo/EFO_0022252 GCST90269718 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in medium LDL percentage (UKB data field 23622) 88,329 European ancestry individuals NA NR [16366144] (imputed) 46 free cholesterol to total lipids in medium LDL percentage http://www.ebi.ac.uk/efo/EFO_0022283 GCST90269719 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in medium LDL percentage (UKB data field 23623) 88,329 European ancestry individuals NA NR [16366144] (imputed) 36 triglycerides to total lipids in medium LDL percentage http://www.ebi.ac.uk/efo/EFO_0022334 GCST90269720 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in small LDL percentage (UKB data field 23624) 88,329 European ancestry individuals NA NR [16366144] (imputed) 25 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269721 Genome-wide genotyping array 2023-06-22 37198478 Pairo-Castineira E 2023-05-17 Nature www.ncbi.nlm.nih.gov/pubmed/37198478 GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19. COVID-19 (critical illness vs population) 682 African ancestry cases, 2,540 African ancestry controls, 401 East Asian ancestry cases, 759 East Asian ancestry controls, 13,199 European ancestry cases, 745,011 European ancestry controls, 1,141 South Asian ancestry cases, 5,384 South Asian ancestry controls, 8,779 cases, 1,001,875 controls NA Illumina [NR] (imputed) 49 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90270934 Genome-wide genotyping array, Genome-wide sequencing 2023-06-22 37198478 Pairo-Castineira E 2023-05-17 Nature www.ncbi.nlm.nih.gov/pubmed/37198478 GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19. COVID-19 (hospitalized covid vs population) 763 African ancestry cases, 24,850 African ancestry controls, 218 admixed American ancestry cases, 94,318 admixed American ancestry controls, 414 East Asian ancestry cases, 816 East Asian ancestry controls, 16,627 European ancestry cases, 749,207 European ancestry controls, 3,533 European, African or admixed American ancestry cases, 1,700 European, African or admixed American ancestry controls, 1,171 South Asian ancestry cases, 5,489 South Asian ancestry controls, 93 other admixed ancestry cases, 645 other admixed ancestry controls, 22,637 cases, 2,052,436 controls NA Illumina [NR] (imputed) 48 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90270935 Genome-wide genotyping array, Genome-wide sequencing 2023-06-22 36759515 Pan H 2023-02-09 NPJ Parkinsons Dis www.ncbi.nlm.nih.gov/pubmed/36759515 Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population. Parkinson's disease 1,972 Chinese ancestry cases, 2,478 Chinese ancestry controls 8,209 Chinese ancestry cases, 9,454 Chinese ancestry controls Illumina [6910086] 19 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90270939 Genome-wide sequencing 2023-08-08 36370000 Senkevich K 2022-11-11 Brain www.ncbi.nlm.nih.gov/pubmed/36370000 GALC variants affect galactosylceramidase enzymatic activity and risk of Parkinson's disease. Galactosylceramidase enzymatic activity 1,454 European or Ashkenazi Jewish ancestry individuals NA Illumina [NR] (imputed) 1 blood galactosylceramidase activity measurement http://www.ebi.ac.uk/efo/EFO_0803535 GCST90270130 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desert hedgehog protein N-product levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 desert hedgehog protein n-product measurement http://www.ebi.ac.uk/efo/EFO_0020319 GCST90247277 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Diablo homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 diablo homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020323 GCST90247278 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dihydropteridine reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247279 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dehydrogenase/reductase SDR family member 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247280 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable ATP-dependent RNA helicase DHX58 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 probable ATP-dependent RNA helicase DHX58 measurement http://www.ebi.ac.uk/efo/EFO_0802901 GCST90247281 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent RNA helicase DHX8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ATP-dependent RNA helicase DHX8 measurement http://www.ebi.ac.uk/efo/EFO_0801398 GCST90247282 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dixin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247283 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dickkopf-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 dickkopf-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020324 GCST90247284 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dickkopf-related protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247285 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dickkopf-related protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247286 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dickkopf-related protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90247287 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dickkopf-related protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 Dickkopf-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008110 GCST90247288 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynein light chain 1, cytoplasmic levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dynein light chain 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020339 GCST90247289 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dihydrolipoyl dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dihydrolipoyl dehydrogenase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0802466 GCST90247290 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disks large homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247291 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disks large homolog 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 disks large homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0802472 GCST90247292 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disks large homolog 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247293 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Delta-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90247294 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Delta-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247295 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Delta-like protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 delta-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020317 GCST90247296 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynein light chain roadblock-type 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 dynein light chain roadblock-type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008114 GCST90247297 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homeobox protein DLX-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247298 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Homeobox protein DLX-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247299 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity mitogen-activated protein kinase kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 dual specificity mitogen-activated protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020335 GCST90247300 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity mitogen-activated protein kinase kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 dual specificity mitogen-activated protein kinase kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008112 GCST90247301 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome c levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cytochrome C measurement http://www.ebi.ac.uk/efo/EFO_0020302 GCST90247227 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. D-3-phosphoglycerate dehydrogenase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247228 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Delta-aminolevulinic acid dehydratase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247229 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. D-amino-acid oxidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247230 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dystroglycan levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dystroglycan measurement http://www.ebi.ac.uk/efo/EFO_0802500 GCST90247231 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Death-associated protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247232 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Death-associated protein kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247233 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Death-associated protein kinase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 death-associated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008107 GCST90247234 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual adapter for phosphotyrosine and 3-phosphotyrosine and 3-phosphoinositide levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247235 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Diamine acetyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 diamine acetyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802464 GCST90247236 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Diamine acetyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 diamine acetyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802465 GCST90247237 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Drebrin-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 drebrin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020333 GCST90247238 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DDB1- and CUL4-associated factor 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DDB1- and CUL4-associated factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0802457 GCST90247239 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Deoxycytidine kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 deoxycytidine kinase measurement http://www.ebi.ac.uk/efo/EFO_0801523 GCST90247240 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DCN1-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247241 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DCN1-like protein 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DCN1-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0802456 GCST90247242 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DCN1-like protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 DCN1-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801520 GCST90247243 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Deoxycytidylate deaminase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247244 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. dCTP pyrophosphatase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DCTP pyrophosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020314 GCST90247245 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. D-dopachrome decarboxylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247246 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247247 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. D-dimer levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 d-dimer measurement http://www.ebi.ac.uk/efo/EFO_0020313 GCST90247248 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA damage-inducible transcript 3 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247249 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA damage-inducible transcript 4 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247250 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0801544 GCST90247251 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage-stimulating protein receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 macrophage-stimulating protein receptor measurement http://www.ebi.ac.uk/efo/EFO_0020550 GCST90248384 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage scavenger receptor types I and II levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90248385 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Medium-chain specific acyl-CoA dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248386 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mothers against decapentaplegic homolog 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248387 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mothers against decapentaplegic homolog 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 mothers against decapentaplegic homolog 4 measurement http://www.ebi.ac.uk/efo/EFO_0801808 GCST90248388 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanoma-associated antigen 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248389 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanoma-associated antigen B10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 melanoma-associated antigen B10 measurement http://www.ebi.ac.uk/efo/EFO_0802735 GCST90248390 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanoma-associated antigen 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 melanoma-associated antigen 10 measurement http://www.ebi.ac.uk/efo/EFO_0801793 GCST90248391 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanoma-associated antigen 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 melanoma-associated antigen 3 measurement http://www.ebi.ac.uk/efo/EFO_0801794 GCST90248392 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanoma-associated antigen 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248393 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanoma-associated antigen 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248394 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802739 GCST90248395 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Malate dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248396 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Malectin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 malectin measurement http://www.ebi.ac.uk/efo/EFO_0802726 GCST90248397 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAM domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 MAM domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802728 GCST90248398 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mesencephalic astrocyte-derived neurotrophic factor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248399 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MANSC domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 MANSC domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801784 GCST90248400 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MANSC domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 MANSC domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0801785 GCST90248401 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MAP/microtubule affinity-regulating kinase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248402 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methionine aminopeptidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 methionine aminopeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008232 GCST90248403 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 mitogen-activated protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020574 GCST90248404 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 mitogen-activated protein kinase 12 measurement http://www.ebi.ac.uk/efo/EFO_0020576 GCST90248405 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 mitogen-activated protein kinase 13 measurement http://www.ebi.ac.uk/efo/EFO_0020577 GCST90248406 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 mitogen-activated protein kinase 14 measurement http://www.ebi.ac.uk/efo/EFO_0020578 GCST90248407 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 mitogen-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020579 GCST90248408 Genome-wide genotyping array 2023-07-21 36929942 Lindstrom S 2023-03-17 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/36929942 Genome-Wide Analyses Characterize Shared Heritability Among Cancers and Identify Novel Cancer Susceptibility Regions. Cancer (pleiotropy) 122,977 European ancestry breast cancer cases, 55,168 European ancestry colorectal cancer cases, 12,906 European ancestry endometrial cancer cases, 4,112 European ancestry esophageal cancer cases, 12,488 European ancestry glioma cancer cases, 6,034 European ancestry head and neck cancer cases, 29,266 European ancestry lung cancer cases, 12,814 European ancestry melanoma cancer cases, 22,406 European ancestry ovarian cancer cases, 8,638 European ancestry pancreatic cancer cases, 79,166 European ancestry prostate cancer cases, 10,784 European ancestry renal cancer cases, 532,864 European ancestry controls NA NR [NR] (imputed) 7 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90274732 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Forearm length to body height ratio 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 20 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270257 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Tibia length to body height ratio 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 30 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270258 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Humerus length to body height ratio 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 26 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270259 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Hip width to body height ratio 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 29 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270260 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Shoulder width to body height ratio 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 10 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270261 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Torso length to body height ratio 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 4 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270262 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Tibiofemoral angle 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 3 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270263 Genome-wide genotyping array 2023-08-09 37471560 Kun E 2023-07-21 Science www.ncbi.nlm.nih.gov/pubmed/37471560 The genetic architecture and evolution of the human skeletal form. Femur length to body height ratio 31,221 British ancestry individuals NA Affymetrix [7387826] (imputed) 23 anthropometric measurement http://www.ebi.ac.uk/efo/EFO_0004302 GCST90270256 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in small LDL (UKB data field 23550) 88,329 European ancestry individuals NA NR [16366144] (imputed) 46 triglycerides in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022323 GCST90269647 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of very large HDL particles (UKB data field 23551) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90269648 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in very large HDL (UKB data field 23552) 88,329 European ancestry individuals NA NR [16366144] (imputed) 45 total lipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022312 GCST90269649 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in very large HDL (UKB data field 23553) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 phospholipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022298 GCST90269650 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in very large HDL (UKB data field 23554) 88,329 European ancestry individuals NA NR [16366144] (imputed) 47 cholesterol in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022229 GCST90269651 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in very large HDL (UKB data field 23555) 88,329 European ancestry individuals NA NR [16366144] (imputed) 49 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269652 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in very large HDL (UKB data field 23556) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 free cholesterol in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022273 GCST90269653 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in very large HDL (UKB data field 23557) 88,329 European ancestry individuals NA NR [16366144] (imputed) 40 triglycerides in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022324 GCST90269654 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of large HDL particles (UKB data field 23558) 88,329 European ancestry individuals NA NR [16366144] (imputed) 55 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90269655 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in large HDL (UKB data field 23559) 88,329 European ancestry individuals NA NR [16366144] (imputed) 59 total lipids in large HDL http://www.ebi.ac.uk/efo/EFO_0022189 GCST90269656 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in large HDL (UKB data field 23560) 88,329 European ancestry individuals NA NR [16366144] (imputed) 58 phospholipids in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022190 GCST90269657 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in large HDL (UKB data field 23561) 88,329 European ancestry individuals NA NR [16366144] (imputed) 59 cholesterol in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0021900 GCST90269658 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in large HDL (UKB data field 23562) 88,329 European ancestry individuals NA NR [16366144] (imputed) 60 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269659 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in large HDL (UKB data field 23563) 88,329 European ancestry individuals NA NR [16366144] (imputed) 59 free cholesterol in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022157 GCST90269660 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in large HDL (UKB data field 23564) 88,329 European ancestry individuals NA NR [16366144] (imputed) 0 triglycerides in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022318 GCST90269661 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of medium HDL particles (UKB data field 23565) 88,329 European ancestry individuals NA NR [16366144] (imputed) 49 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90269662 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in medium HDL (UKB data field 23566) 88,329 European ancestry individuals NA NR [16366144] (imputed) 47 total lipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022310 GCST90269663 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in medium HDL (UKB data field 23567) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 phospholipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022295 GCST90269664 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol in medium HDL (UKB data field 23568) 88,329 European ancestry individuals NA NR [16366144] (imputed) 49 cholesterol in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0021903 GCST90269665 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters in medium HDL (UKB data field 23569) 88,329 European ancestry individuals NA NR [16366144] (imputed) 50 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90269666 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol in medium HDL (UKB data field 23570) 88,329 European ancestry individuals NA NR [16366144] (imputed) 48 free cholesterol in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022267 GCST90269667 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides in medium HDL (UKB data field 23571) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 triglycerides in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022321 GCST90269668 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Concentration of small HDL particles (UKB data field 23572) 88,329 European ancestry individuals NA NR [16366144] (imputed) 25 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90269669 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Total lipids in small HDL (UKB data field 23573) 88,329 European ancestry individuals NA NR [16366144] (imputed) 23 total lipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022311 GCST90269670 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids in small HDL (UKB data field 23574) 88,329 European ancestry individuals NA NR [16366144] (imputed) 24 phospholipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022296 GCST90269671 Genome-wide genotyping array 2023-06-22 36788602 Li S 2023-02-14 Genome Med www.ncbi.nlm.nih.gov/pubmed/36788602 Ultra-low-coverage genome-wide association study-insights into gestational age using 17,844 embryo samples with preimplantation genetic testing. Gestational age (fetal effect) 1,744 Chinese ancestry embryos NA Illumina [1107198] (imputed) 15 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST90271320 Genome-wide sequencing 2023-08-10 33559384 Zhong X 2021-02-08 Eur J Neurol www.ncbi.nlm.nih.gov/pubmed/33559384 Whole-exome sequencing reveals the major genetic factors contributing to neuromyelitis optica spectrum disorder in Chinese patients with aquaporin 4-IgG seropositivity. Neuromyelitis optica spectrum disorder (AQP4-IgG-positive) 228 Chinese ancestry cases, 1,400 Chinese ancestry controls NA Illumina [2010184] 1 AQP4-IgG-positive neuromyelitis optica http://www.ebi.ac.uk/efo/EFO_0009584 GCST90277235 Exome-wide sequencing 2023-10-12 36928559 Ye Y 2023-03-16 Geroscience www.ncbi.nlm.nih.gov/pubmed/36928559 A genome-wide association study of frailty identifies significant genetic correlation with neuropsychiatric, cardiovascular, and inflammation pathways. Fried Frailty Score 386,565 European ancestry individuals 9,720 European ancestry individuals Affymetrix [8883488] (imputed) 0 frailty measurement http://www.ebi.ac.uk/efo/EFO_0009885 GCST90295968 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in small LDL percentage (UKB data field 23625) 88,329 European ancestry individuals NA NR [16366144] (imputed) 20 cholesterol to total lipids in small LDL percentage http://www.ebi.ac.uk/efo/EFO_0022241 GCST90269722 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in small LDL percentage (UKB data field 23626) 88,329 European ancestry individuals NA NR [16366144] (imputed) 29 cholesteryl esters to total lipids in small LDL percentage http://www.ebi.ac.uk/efo/EFO_0022255 GCST90269723 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in small LDL percentage (UKB data field 23627) 88,329 European ancestry individuals NA NR [16366144] (imputed) 38 free cholesterol to total lipids in small LDL percentage http://www.ebi.ac.uk/efo/EFO_0022286 GCST90269724 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in small LDL percentage (UKB data field 23628) 88,329 European ancestry individuals NA NR [16366144] (imputed) 45 triglycerides to total lipids in small LDL percentage http://www.ebi.ac.uk/efo/EFO_0022337 GCST90269725 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in very large HDL percentage (UKB data field 23629) 88,307 European ancestry individuals NA NR [16366139] (imputed) 37 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269726 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in very large HDL percentage (UKB data field 23630) 88,307 European ancestry individuals NA NR [16366139] (imputed) 24 cholesterol to total lipids in very large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022243 GCST90269727 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in very large HDL percentage (UKB data field 23631) 88,307 European ancestry individuals NA NR [16366139] (imputed) 27 cholesteryl esters to total lipids in very large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022257 GCST90269728 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in very large HDL percentage (UKB data field 23632) 88,307 European ancestry individuals NA NR [16366139] (imputed) 39 free cholesterol to total lipids in very large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022288 GCST90269729 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in very large HDL percentage (UKB data field 23633) 88,307 European ancestry individuals NA NR [16366139] (imputed) 44 triglycerides to total lipids in very large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022339 GCST90269730 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in large HDL percentage (UKB data field 23634) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269731 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in large HDL percentage (UKB data field 23635) 88,329 European ancestry individuals NA NR [16366144] (imputed) 41 cholesterol to total lipids in large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022234 GCST90269732 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in large HDL percentage (UKB data field 23636) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 cholesteryl esters to total lipids in large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022248 GCST90269733 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in large HDL percentage (UKB data field 23637) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 free cholesterol to total lipids in large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022279 GCST90269734 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in large HDL percentage (UKB data field 23638) 88,329 European ancestry individuals NA NR [16366144] (imputed) 43 triglycerides to total lipids in large HDL percentage http://www.ebi.ac.uk/efo/EFO_0022330 GCST90269735 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in medium HDL percentage (UKB data field 23639) 88,329 European ancestry individuals NA NR [16366144] (imputed) 54 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269736 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in medium HDL percentage (UKB data field 23640) 88,329 European ancestry individuals NA NR [16366144] (imputed) 47 cholesterol to total lipids in medium HDL percentage http://www.ebi.ac.uk/efo/EFO_0022237 GCST90269737 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in medium HDL percentage (UKB data field 23641) 88,329 European ancestry individuals NA NR [16366144] (imputed) 42 cholesteryl esters to total lipids in medium HDL percentage http://www.ebi.ac.uk/efo/EFO_0022251 GCST90269738 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in medium HDL percentage (UKB data field 23642) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 free cholesterol to total lipids in medium HDL percentage http://www.ebi.ac.uk/efo/EFO_0022282 GCST90269739 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in medium HDL percentage (UKB data field 23643) 88,329 European ancestry individuals NA NR [16366144] (imputed) 44 triglycerides to total lipids in medium HDL percentage http://www.ebi.ac.uk/efo/EFO_0022333 GCST90269740 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Phospholipids to total lipids in small HDL percentage (UKB data field 23644) 88,329 European ancestry individuals NA NR [16366144] (imputed) 32 phospholipids:total lipids ratio http://www.ebi.ac.uk/efo/EFO_0020946 GCST90269741 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesterol to total lipids in small HDL percentage (UKB data field 23645) 88,329 European ancestry individuals NA NR [16366144] (imputed) 35 cholesterol to total lipids in small HDL percentage http://www.ebi.ac.uk/efo/EFO_0022240 GCST90269742 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Cholesteryl esters to total lipids in small HDL percentage (UKB data field 23646) 88,329 European ancestry individuals NA NR [16366144] (imputed) 32 cholesteryl esters to total lipids in small HDL percentage http://www.ebi.ac.uk/efo/EFO_0022254 GCST90269743 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Free cholesterol to total lipids in small HDL percentage (UKB data field 23647) 88,329 European ancestry individuals NA NR [16366144] (imputed) 39 free cholesterol to total lipids in small HDL percentage http://www.ebi.ac.uk/efo/EFO_0022285 GCST90269744 Genome-wide genotyping array 2023-08-31 36764567 Davyson E 2023-02-09 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36764567 Metabolomic Investigation of Major Depressive Disorder Identifies a Potentially Causal Association With Polyunsaturated Fatty Acids. Triglycerides to total lipids in small HDL percentage (UKB data field 23648) 88,329 European ancestry individuals NA NR [16366144] (imputed) 53 triglycerides to total lipids in small HDL percentage http://www.ebi.ac.uk/efo/EFO_0022336 GCST90269745 Genome-wide genotyping array 2023-06-22 36762557 Xie Y 2023-02-10 Stroke www.ncbi.nlm.nih.gov/pubmed/36762557 Whole-Exome Sequencing Analyses Support a Role of Vitamin D Metabolism in Ischemic Stroke. Ischemic stroke 1,777 European ancestry cases, 150,281 European ancestry controls NA Affymetrix [17121251] (imputed) 1 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90271319 Genome-wide genotyping array 2023-11-13 37209533 Hess T 2023-05-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/37209533 Dissecting the genetic heterogeneity of gastric cancer. Gastric cancer 5,815 European ancestry cases, 10,999 European ancestry controls NA NR [7829683] (imputed) 5 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90296724 Genome-wide genotyping array 2023-11-13 37209533 Hess T 2023-05-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/37209533 Dissecting the genetic heterogeneity of gastric cancer. Cardia gastric cancer 1,291 European ancestry cases, 10,999 European ancestry controls NA NR [7829683] (imputed) 0 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90296725 Genome-wide genotyping array 2023-11-13 37209533 Hess T 2023-05-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/37209533 Dissecting the genetic heterogeneity of gastric cancer. Non-cardia gastric cancer 3,183 European ancestry cases, 10,999 European ancestry controls NA NR [7829683] (imputed) 4 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90296726 Genome-wide genotyping array 2023-11-13 37209533 Hess T 2023-05-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/37209533 Dissecting the genetic heterogeneity of gastric cancer. Diffuse gastric cancer 1,308 European ancestry cases, 10,999 European ancestry controls NA NR [7829683] (imputed) 3 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90296727 Genome-wide genotyping array 2023-11-13 37209533 Hess T 2023-05-18 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/37209533 Dissecting the genetic heterogeneity of gastric cancer. Intestinal gastric cancer 1,696 European ancestry cases, 10,999 European ancestry controls NA NR [7829683] (imputed) 4 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90296728 Genome-wide genotyping array 2023-06-28 36911400 Shih CH 2023-02-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/36911400 Genome-wide association study and identification of systemic comorbidities in development of age-related macular degeneration in a hospital-based cohort of Han Chinese. Age-related macular degeneration 339 Han Chinese ancestry cases, 3,390 Han Chinese ancestry controls NA NR [467342] 11 age-related macular degeneration http://www.ebi.ac.uk/efo/EFO_0001365 GCST90271581 Genome-wide genotyping array 2023-11-14 37218628 Zhou S 2023-05-23 Psychol Med www.ncbi.nlm.nih.gov/pubmed/37218628 Investigating the shared genetic architecture of post-traumatic stress disorder and gastrointestinal tract disorders: a genome-wide cross-trait analysis. Post-traumatic stress disorder (MTAG) at least 23,212 European ancestry cases, at least 151,447 European ancestry controls (MTAG boosted by gastrointestinal tract disorder samples) NA NR [6443162] (imputed) 16 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90297545 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclic nucleotide-gated olfactory channel levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247077 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CCR4-NOT transcription complex subunit 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CCR4-NOT transcription complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0802377 GCST90247078 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CB1 cannabinoid receptor-interacting protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247079 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ciliary neurotrophic factor receptor subunit alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ciliary neurotrophic factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020261 GCST90247080 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Contactin-associated protein-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 contactin-associated protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0801496 GCST90247081 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Contactin-associated protein-like 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247082 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-1(I) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 collagen alpha-1(I) chain measurement http://www.ebi.ac.uk/efo/EFO_0801486 GCST90247083 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-1(IX) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247084 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-1(VI) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 collagen alpha-1(VI) chain measurement http://www.ebi.ac.uk/efo/EFO_0801487 GCST90247085 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-1(X) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247086 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-1(XIII) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247087 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-1(XV) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 collagen alpha-1(XV) chain measurement http://www.ebi.ac.uk/efo/EFO_0801488 GCST90247088 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-1(XXVIII) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 collagen alpha-1(XXVIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0802420 GCST90247089 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-2(VI) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247090 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-2(XI) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 collagen alpha-2(XI) chain measurement http://www.ebi.ac.uk/efo/EFO_0801490 GCST90247091 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Collagen alpha-3(VI) chain levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 collagen alpha-3(VI) chain measurement http://www.ebi.ac.uk/efo/EFO_0802421 GCST90247092 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome c oxidase assembly factor 3 homolog, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cytochrome c oxidase assembly factor 3 homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0801513 GCST90247093 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coactosin-like protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 coactosin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020262 GCST90247094 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Glutaryl-CoA dehydrogenase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247095 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation factor IX levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 coagulation factor IX measurement http://www.ebi.ac.uk/efo/EFO_0020263 GCST90247096 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation factor IXab levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 coagulation factor IXAB measurement http://www.ebi.ac.uk/efo/EFO_0020264 GCST90247097 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation Factor V levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST90247098 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation Factor VII levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247099 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation Factor VIII levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247100 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Coagulation Factor X levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 coagulation factor X measurement http://www.ebi.ac.uk/efo/EFO_0020265 GCST90247101 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and coronary artery disease 432,109 European ancestry individuals, 184,305 individuals NA NR [NR] 0 neuroticism measurement, coronary artery disease http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0001645 GCST90020169 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and body mass index 771,333 European ancestry individuals NA NR [NR] 0 neuroticism measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90020170 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and diastolic blood pressure 501,504 European ancestry individuals NA NR [NR] 0 diastolic blood pressure, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0006336, http://www.ebi.ac.uk/efo/EFO_0007660 GCST90020171 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and systolic blood pressure 501,504 European ancestry individuals NA NR [NR] 0 systolic blood pressure, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0006335, http://www.ebi.ac.uk/efo/EFO_0007660 GCST90020172 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and waist-hip ratio 656,568 European ancestry individuals NA NR [NR] 0 neuroticism measurement, waist height ratio http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0005191 GCST90020173 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and high density lipoprotein levels 620,686 European ancestry individuals NA NR [NR] 0 neuroticism measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90020174 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and total cholesterol levels 620,686 European ancestry individuals NA NR [NR] 0 total cholesterol measurement, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0007660 GCST90020175 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and triglyceride levels 620,686 European ancestry individuals NA NR [NR] 0 triglyceride measurement, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0007660 GCST90020176 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and type 2 diabetes 458,785 European ancestry cases, 132,532 European ancestry controls NA NR [NR] 0 neuroticism measurement, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0007660, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90020177 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and C-reactive protein levels 636,511 European ancestry individuals NA NR [NR] 0 neuroticism measurement, C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0004458 GCST90020178 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and low density lipoprotein levels 620,686 European ancestry individuals NA NR [NR] 0 neuroticism measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90020179 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and pulse pressure 501,504 European ancestry individuals NA NR [NR] 0 pulse pressure measurement, neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0005763, http://www.ebi.ac.uk/efo/EFO_0007660 GCST90020180 Genome-wide genotyping array 2023-03-29 34226488 Torgersen K 2021-06-17 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/34226488 Shared genetic architecture between neuroticism, coronary artery disease and cardiovascular risk factors. Neuroticism and smoking behaviour (cigarettes smoked per day) 506,162 European ancestry individuals NA NR [NR] 0 neuroticism measurement, cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0006525 GCST90020181 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity mitogen-activated protein kinase kinase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 dual specificity mitogen-activated protein kinase kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0008113 GCST90247302 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247303 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 disintegrin and metalloproteinase domain-containing protein 11 measurement http://www.ebi.ac.uk/efo/EFO_0801529 GCST90247304 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247305 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 disintegrin and metalloproteinase domain-containing protein 19 measurement http://www.ebi.ac.uk/efo/EFO_0802470 GCST90247306 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 22 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247307 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 disintegrin and metalloproteinase domain-containing protein 23 measurement http://www.ebi.ac.uk/efo/EFO_0801530 GCST90247308 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 30 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247309 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 32 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247310 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Disintegrin and metalloproteinase domain-containing protein 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247311 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dynein intermediate chain 1, axonemal levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247312 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Delta and Notch-like epidermal growth factor-related receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 delta and Notch-like epidermal growth factor-related receptor measurement http://www.ebi.ac.uk/efo/EFO_0802458 GCST90247313 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily A member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247314 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily A member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DnaJ homolog subfamily A member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802486 GCST90247315 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DNAj homolog subfamily b member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020332 GCST90247316 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 DnaJ homolog subfamily B member 11 measurement http://www.ebi.ac.uk/efo/EFO_0801537 GCST90247317 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 12 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DnaJ homolog subfamily B member 12 measurement http://www.ebi.ac.uk/efo/EFO_0802487 GCST90247318 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DnaJ homolog subfamily B member 14 measurement http://www.ebi.ac.uk/efo/EFO_0801538 GCST90247319 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DnaJ homolog subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0801539 GCST90247320 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247321 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247322 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily B member 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 DnaJ homolog subfamily B member 9 measurement http://www.ebi.ac.uk/efo/EFO_0801540 GCST90247323 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 10 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DnaJ homolog subfamily C member 10 measurement http://www.ebi.ac.uk/efo/EFO_0802488 GCST90247324 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247325 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 15 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DnaJ homolog subfamily C member 15 measurement http://www.ebi.ac.uk/efo/EFO_0802489 GCST90247326 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent RNA helicase DDX19A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247252 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent RNA helicase DDX19B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ATP-dependent rna helicase ddx19b measurement http://www.ebi.ac.uk/efo/EFO_0020167 GCST90247253 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable ATP-dependent RNA helicase DDX23 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247254 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. ATP-dependent RNA helicase DDX25 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 ATP-dependent RNA helicase DDX25 measurement http://www.ebi.ac.uk/efo/EFO_0802295 GCST90247255 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable ATP-dependent RNA helicase DDX46 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247256 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable ATP-dependent RNA helicase DDX58 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 probable ATP-dependent RNA helicase DDX58 measurement http://www.ebi.ac.uk/efo/EFO_0801913 GCST90247257 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Probable ATP-dependent RNA helicase DDX6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247258 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Deformed epidermal autoregulatory factor 1 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 deformed epidermal autoregulatory factor 1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0801522 GCST90247259 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Decorin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 decorin measurement http://www.ebi.ac.uk/efo/EFO_0020315 GCST90247260 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Defensin-5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247261 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Differentially expressed in FDCP 6 homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247262 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein DEPP levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein DEPP measurement http://www.ebi.ac.uk/efo/EFO_0801939 GCST90247263 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Derlin-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 derlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0802461 GCST90247264 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dermatopontin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90247265 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dermokine levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 dermokine measurement http://www.ebi.ac.uk/efo/EFO_0802462 GCST90247266 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desmin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247267 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desmoglein-1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 desmoglein-1 measurement http://www.ebi.ac.uk/efo/EFO_0020321 GCST90247268 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desmoglein-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 desmoglein-2 measurement http://www.ebi.ac.uk/efo/EFO_0020322 GCST90247269 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Desmoglein-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247270 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein DGCR14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein DGCR14 measurement http://www.ebi.ac.uk/efo/EFO_0801940 GCST90247271 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. D-glucuronyl C5-epimerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 D-glucuronyl C5-epimerase measurement http://www.ebi.ac.uk/efo/EFO_0801519 GCST90247272 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein DGCR6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein DGCR6 measurement http://www.ebi.ac.uk/efo/EFO_0802931 GCST90247273 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Diacylglycerol kinase beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 diacylglycerol kinase beta measurement http://www.ebi.ac.uk/efo/EFO_0801525 GCST90247274 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 17-beta-hydroxysteroid dehydrogenase 14 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 17-beta-hydroxysteroid dehydrogenase 14 measurement http://www.ebi.ac.uk/efo/EFO_0802231 GCST90247275 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 3-keto-steroid reductase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247276 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247327 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 DnaJ homolog subfamily C member 17 measurement http://www.ebi.ac.uk/efo/EFO_0801541 GCST90247328 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 27 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 DnaJ homolog subfamily C member 27 measurement http://www.ebi.ac.uk/efo/EFO_0802491 GCST90247329 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 30 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 DnaJ homolog subfamily C member 30 measurement http://www.ebi.ac.uk/efo/EFO_0801542 GCST90247330 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DnaJ homolog subfamily C member 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 DnaJ homolog subfamily C member 4 measurement http://www.ebi.ac.uk/efo/EFO_0802492 GCST90247331 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA (cytosine-5)-methyltransferase 3-like levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247332 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Deoxyribonuclease-2-beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 deoxyribonuclease-2-beta measurement http://www.ebi.ac.uk/efo/EFO_0802460 GCST90247333 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Deoxyribonuclease-1-like 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247334 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Double C2-like domain-containing protein beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247335 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dedicator of cytokinesis protein 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 dedicator of cytokinesis protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0801521 GCST90247336 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Docking protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247337 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Docking protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 docking protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801543 GCST90247338 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Histone-lysine N-methyltransferase, H3 lysine-79 specific levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247339 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DCC-interacting protein 13-alpha levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DCC-interacting protein 13-alpha measurement http://www.ebi.ac.uk/efo/EFO_0802455 GCST90247340 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dipeptidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 dipeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0802469 GCST90247341 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dipeptidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 dipeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0801528 GCST90247342 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA polymerase iota levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DNA polymerase iota measurement http://www.ebi.ac.uk/efo/EFO_0802476 GCST90247343 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA polymerase epsilon subunit 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247344 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA polymerase epsilon subunit 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247345 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. DNA-directed DNA/RNA polymerase mu levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 DNA-directed DNA/RNA polymerase mu measurement http://www.ebi.ac.uk/efo/EFO_0802485 GCST90247346 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dipeptidyl peptidase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 dipeptidyl peptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020325 GCST90247347 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual 3,5-cyclic-AMP and -GMP phosphodiesterase 11A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247348 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dipeptidyl peptidase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90247349 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dipeptidyl peptidase 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247350 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Diphosphomevalonate decarboxylase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247351 Genome-wide genotyping array 2023-09-01 37494057 Sun Q 2023-07-26 JAMA Dermatol www.ncbi.nlm.nih.gov/pubmed/37494057 Genetic Variants Associated With Hidradenitis Suppurativa. Hidradenitis suppurativa 1,640 European ancestry, African American or Afro-Caribbean, NR cases, 756,393 European ancestry, African American or Afro-Caribbean, NR controls 189 European ancestry cases, 64,234 European ancestry controls, 101 African American or Afro-Caribbean cases, 12,105 African American or Afro-Caribbean controls NR [8340278] (imputed) 3 hidradenitis suppurativa http://www.ebi.ac.uk/efo/EFO_1000710 GCST90278188 Genome-wide genotyping array 2023-09-01 37494057 Sun Q 2023-07-26 JAMA Dermatol www.ncbi.nlm.nih.gov/pubmed/37494057 Genetic Variants Associated With Hidradenitis Suppurativa. Hidradenitis suppurativa 317 European ancestry cases, 3,868 European ancestry controls NA Illumina [NR] (imputed) 5 hidradenitis suppurativa http://www.ebi.ac.uk/efo/EFO_1000710 GCST90281023 Genome-wide genotyping array 2023-09-01 37494057 Sun Q 2023-07-26 JAMA Dermatol www.ncbi.nlm.nih.gov/pubmed/37494057 Genetic Variants Associated With Hidradenitis Suppurativa. Hidradenitis suppurativa 247 African American or Afro-Caribbean cases, 707 African American or Afro-Caribbean controls NA Illumina [NR] (imputed) 2 hidradenitis suppurativa http://www.ebi.ac.uk/efo/EFO_1000710 GCST90281024 Genome-wide genotyping array 2023-08-21 37094658 Alemany-Navarro M 2023-04-23 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37094658 The genomics of visuospatial neurocognition in obsessive-compulsive disorder: A preliminary GWAS. Neurocognitive measure (immediate recall) in obsessive-compulsive disorder 127 Spanish ancestry individuals NA Illumina [2661707] (imputed) 12 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST90277980 Genome-wide genotyping array 2023-08-21 37094658 Alemany-Navarro M 2023-04-23 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37094658 The genomics of visuospatial neurocognition in obsessive-compulsive disorder: A preliminary GWAS. Neurocognitive measure (delayed recall) in obsessive-compulsive disorder 127 Spanish ancestry individuals NA Illumina [2661707] (imputed) 10 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST90277981 Genome-wide genotyping array 2023-08-21 37094658 Alemany-Navarro M 2023-04-23 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37094658 The genomics of visuospatial neurocognition in obsessive-compulsive disorder: A preliminary GWAS. Neurocognitive measure (copy accuracy) in obsessive-compulsive disorder 127 Spanish ancestry individuals NA Illumina [2661707] (imputed) 7 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST90277982 Genome-wide genotyping array 2023-08-21 37094658 Alemany-Navarro M 2023-04-23 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37094658 The genomics of visuospatial neurocognition in obsessive-compulsive disorder: A preliminary GWAS. Neurocognitive measure (copy organization) in obsessive-compulsive disorder 127 Spanish ancestry individuals NA Illumina [2661707] (imputed) 12 obsessive-compulsive disorder http://www.ebi.ac.uk/efo/EFO_0004242 GCST90277983 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 4 member A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247052 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 4 member C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247053 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 4 member D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 C-type lectin domain family 4 member D measurement http://www.ebi.ac.uk/efo/EFO_0802347 GCST90247054 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 4 member G levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247055 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 4 member M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 C-type lectin domain family 4 member M measurement http://www.ebi.ac.uk/efo/EFO_0020202 GCST90247056 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 6 member A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-type lectin domain family 6 member A measurement http://www.ebi.ac.uk/efo/EFO_0802348 GCST90247057 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-type lectin domain family 7 member A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-type lectin domain family 7 member A measurement http://www.ebi.ac.uk/efo/EFO_0802349 GCST90247058 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calmegin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247059 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Clathrin heavy chain 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 clathrin heavy chain 1 measurement http://www.ebi.ac.uk/efo/EFO_0802402 GCST90247060 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Clathrin interactor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 clathrin interactor 1 measurement http://www.ebi.ac.uk/efo/EFO_0801478 GCST90247061 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chloride intracellular channel protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 chloride intracellular channel protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802392 GCST90247062 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Chloride intracellular channel protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 chloride intracellular channel protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0801472 GCST90247063 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Dual specificity protein kinase CLK2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 dual specificity protein kinase CLK2 measurement http://www.ebi.ac.uk/efo/EFO_0801548 GCST90247064 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Ceroid-lipofuscinosis neuronal protein 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 ceroid-lipofuscinosis neuronal protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0802390 GCST90247065 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Clusterin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007655 GCST90247066 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cation-independent mannose-6-phosphate receptor levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90247067 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Carboxymethylenebutenolidase homolog levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247068 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801479 GCST90247069 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0802403 GCST90247070 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CMRF35-like molecule 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CMRF35-like molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0802405 GCST90247071 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CMRF35-like molecule 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90247072 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CMRF35-like molecule 7 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CMRF35-like molecule 7 measurement http://www.ebi.ac.uk/efo/EFO_0802407 GCST90247073 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CMRF35-like molecule 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 CMRF35-like molecule 8 measurement http://www.ebi.ac.uk/efo/EFO_0801480 GCST90247074 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. 2,3-cyclic-nucleotide 3-phosphodiesterase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 2',3'-cyclic-nucleotide 3'-phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0802232 GCST90247075 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytosolic non-specific dipeptidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cytosolic non-specific dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020310 GCST90247076 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CREB-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 CREB-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801502 GCST90247152 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein CREG1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein CREG1 measurement http://www.ebi.ac.uk/efo/EFO_0801937 GCST90247153 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine-rich with EGF-like domain protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cysteine-rich with EGF-like domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021870 GCST90247154 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Corticotropin-releasing factor-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 corticotropin-releasing factor-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801501 GCST90247155 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine-rich motor neuron 1 protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cysteine-rich motor neuron 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0802446 GCST90247156 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine-rich protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247157 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine-rich protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247158 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine-rich PDZ-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247159 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine-rich secretory protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 cysteine-rich secretory protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801511 GCST90247160 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Adapter molecule crk levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 adapter molecule CRK measurement http://www.ebi.ac.uk/efo/EFO_0020128 GCST90247161 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cysteine-rich secretory protein LCCL domain-containing 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cysteine-rich secretory protein LCCL domain-containing 2 measurement http://www.ebi.ac.uk/efo/EFO_0801512 GCST90247162 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytokine receptor-like factor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cytokine receptor-like factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0802454 GCST90247163 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytokine receptor-like factor 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cytokine receptor-like factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020306 GCST90247164 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-reactive protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90247165 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. cAMP-regulated phosphoprotein 19 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cAMP-regulated phosphoprotein 19 measurement http://www.ebi.ac.uk/efo/EFO_0020223 GCST90247166 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement receptor type 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 10 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247167 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Complement receptor type 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247168 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytotoxic and regulatory T-cell molecule levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cytotoxic and regulatory t-cell molecule measurement http://www.ebi.ac.uk/efo/EFO_0020311 GCST90247169 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cryptic protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cryptic protein measurement http://www.ebi.ac.uk/efo/EFO_0020293 GCST90247170 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. cAMP-specific 3,5-cyclic phosphodiesterase 4A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247171 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cold shock domain-containing protein C2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cold shock domain-containing protein C2 measurement http://www.ebi.ac.uk/efo/EFO_0802415 GCST90247172 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cold shock domain-containing protein E1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cold shock domain-containing protein E1 measurement http://www.ebi.ac.uk/efo/EFO_0802416 GCST90247173 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CUB and sushi domain-containing protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 CUB and Sushi domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0803297 GCST90247174 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. CUB and sushi domain-containing protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 CUB and Sushi domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803314 GCST90247175 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Casein kinase I isoform delta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 casein kinase I isoform delta measurement http://www.ebi.ac.uk/efo/EFO_0802372 GCST90247176 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 11 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90247202 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 13 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 C-X-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020205 GCST90247203 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 16 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90247204 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 17 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247205 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-X-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008058 GCST90247206 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 6 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90247207 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. C-X-C motif chemokine 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 C-X-C motif chemokine 9 measurement http://www.ebi.ac.uk/efo/EFO_0022032 GCST90247208 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Calcyclin-binding protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 calcyclin-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0801443 GCST90247209 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-H levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cyclin-H measurement http://www.ebi.ac.uk/efo/EFO_0801508 GCST90247210 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-A1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247211 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cyclin-A2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247212 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytohesin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 cytohesin-2 measurement http://www.ebi.ac.uk/efo/EFO_0801517 GCST90247213 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Protein CYR61 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein CYR61 measurement http://www.ebi.ac.uk/efo/EFO_0802929 GCST90247214 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cystatin-8 measurement http://www.ebi.ac.uk/efo/EFO_0801509 GCST90247215 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247216 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-D levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90247217 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-F levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 10 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90247218 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-like 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247219 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-M levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90247220 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-S levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cystatin-S measurement http://www.ebi.ac.uk/efo/EFO_0020300 GCST90247221 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-SA levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cystatin-SA measurement http://www.ebi.ac.uk/efo/EFO_0008105 GCST90247222 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cystatin-SN levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 cystatin-SN measurement http://www.ebi.ac.uk/efo/EFO_0008106 GCST90247223 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytosol aminopeptidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247224 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytokine-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90247225 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Cytochrome b5 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 cytochrome b5 measurement http://www.ebi.ac.uk/efo/EFO_0802448 GCST90247226 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysozyme C levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90248359 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysozyme g-like protein 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lysozyme g-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0801778 GCST90248360 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysozyme-like protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 lysozyme-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0801779 GCST90248361 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. LysM and putative peptidoglycan-binding domain-containing protein 4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lysM and putative peptidoglycan-binding domain-containing protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0802718 GCST90248362 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysosome membrane protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 lysosome membrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020545 GCST90248363 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysyl oxidase homolog 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 lysyl oxidase homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0802721 GCST90248364 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysyl oxidase homolog 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248365 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysosomal protective protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90248366 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysosomal Pro-X carboxypeptidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 lysosomal Pro-X carboxypeptidase measurement http://www.ebi.ac.uk/efo/EFO_0801777 GCST90248367 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lysine--tRNA ligase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248368 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Lymphatic vessel endothelial hyaluronic acid receptor 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 7 lymphatic vessel endothelial hyaluronic acid receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020539 GCST90248369 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Melanocortin-2 receptor accessory protein 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 melanocortin-2 receptor accessory protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0802733 GCST90248370 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase kinase kinase kinase 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248371 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase kinase kinase kinase 3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248372 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mannosyl-oligosaccharide 1,2-alpha-mannosidase IB levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 8 mannosyl-oligosaccharide 1,2-alpha-mannosidase IB measurement http://www.ebi.ac.uk/efo/EFO_0801783 GCST90248373 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mannosyl-oligosaccharide 1,2-alpha-mannosidase IC levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248374 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microtubule-associated proteins 1A/1B light chain 3A levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 9 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248375 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microtubule-associated proteins 1A/1B light chain 3B levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248376 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase measurement http://www.ebi.ac.uk/efo/EFO_0801568 GCST90248377 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mycophenolic acid acyl-glucuronide esterase, mitochondrial levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248378 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Maleylacetoacetate isomerase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248379 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. O-acetyl-ADP-ribose deacetylase MACROD1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 o-acetyl-ADP-ribose deacetylase MACROD1 measurement http://www.ebi.ac.uk/efo/EFO_0802827 GCST90248380 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macoilin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 macoilin measurement http://www.ebi.ac.uk/efo/EFO_0802722 GCST90248381 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage-capping protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 macrophage-capping protein measurement http://www.ebi.ac.uk/efo/EFO_0020549 GCST90248382 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrosialin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248383 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase 8 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 mitogen-activated protein kinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020580 GCST90248409 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mitogen-activated protein kinase 9 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 mitogen-activated protein kinase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020581 GCST90248410 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Membrane-associated progesterone receptor component 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 membrane-associated progesterone receptor component 1 measurement http://www.ebi.ac.uk/efo/EFO_0802740 GCST90248411 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Membrane-associated progesterone receptor component 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 membrane-associated progesterone receptor component 2 measurement http://www.ebi.ac.uk/efo/EFO_0801796 GCST90248412 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. MARCKS-related protein levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248413 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Macrophage receptor MARCO levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248414 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microtubule-associated protein RP/EB family member 1 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248415 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microtubule-associated protein RP/EB family member 2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248416 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Maspardin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 1 maspardin measurement http://www.ebi.ac.uk/efo/EFO_0801786 GCST90248417 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Mast/stem cell growth factor receptor Kit levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 5 mast/stem cell growth factor receptor kit measurement http://www.ebi.ac.uk/efo/EFO_0020554 GCST90248418 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Methionine adenosyltransferase 2 subunit beta levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248419 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Microtubule-associated protein tau levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 microtubule-associated protein tau measurement http://www.ebi.ac.uk/efo/EFO_0020570 GCST90248420 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Megakaryocyte-associated tyrosine-protein kinase levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 megakaryocyte-associated tyrosine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0020562 GCST90248421 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrilin-2 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248422 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrilin-3 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 4 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248423 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrilin-4 levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90248424 Genome-wide genotyping array 2023-04-03 34648354 Pietzner M 2021-11-12 Science www.ncbi.nlm.nih.gov/pubmed/34648354 Mapping the proteo-genomic convergence of human diseases. Matrilysin levels 10,708 European ancestry individuals NA Affymetrix, Illumina [10200000] (imputed) 3 matrilysin measurement http://www.ebi.ac.uk/efo/EFO_0008227 GCST90248425 Genome-wide genotyping array 2023-06-23 36750564 Khunsriraksakul C 2023-02-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36750564 Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus. Systemic lupus erythematosus (MTAG) at least 5,877 East Asian ancestry cases, at least 188,588 East Asian ancestry controls, at least 14,355 European ancestry cases, at least 505,956 European ancestry controls, at least 1,393 admixed American ancestry cases, at least 2,327 admixed American ancestry controls (MTAG boosted by autoimmune diseases samples) NA NR [NR] 249 systemic lupus erythematosus http://purl.obolibrary.org/obo/MONDO_0007915 GCST90270940 Genome-wide genotyping array 2023-08-18 36941031 Alonso N 2023-03-20 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36941031 Genome-wide association study identifies genetic variants which predict the response of bone mineral density to teriparatide therapy. Response of lumbar spine BMD to teriparatide in osteoporosis 437 individuals NA Affymetrix [NR] 3 trait in response to teriparatide, spine bone mineral density http://purl.obolibrary.org/obo/OBA_2050330, http://www.ebi.ac.uk/efo/EFO_0007701 GCST90271958 Genome-wide genotyping array 2023-08-18 36941031 Alonso N 2023-03-20 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36941031 Genome-wide association study identifies genetic variants which predict the response of bone mineral density to teriparatide therapy. Response of femoral neck BMD to teriparatide in osteoporosis 437 individuals NA Affymetrix [NR] 2 trait in response to teriparatide, femoral neck bone mineral density http://purl.obolibrary.org/obo/OBA_2050330, http://www.ebi.ac.uk/efo/EFO_0007785 GCST90271959 Genome-wide genotyping array 2023-06-28 34454985 Sliz E 2021-08-26 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/34454985 Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis. Atopic dermatitis 22,474 European ancestry cases, 774,187 European ancestry controls NA Affymetrix, Illumina [16201029] (imputed) 30 atopic eczema http://www.ebi.ac.uk/efo/EFO_0000274 GCST90027161 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:146:T:C case-only heteroplasmy) 1,151 European ancestry individuals NA Affymetrix [9285673] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268462 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:152:T:C case-only heteroplasmy) 956 European ancestry individuals NA Affymetrix [8992293] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268463 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:204:T:C case-only heteroplasmy) 1,130 European ancestry individuals NA Affymetrix [9259078] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268464 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:C case-only heteroplasmy) 474 European ancestry individuals NA Affymetrix [7860564] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268465 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:302:AC:A case-only heteroplasmy) 538 European ancestry individuals NA Affymetrix [8068328] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268466 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:302:A:AC case-only heteroplasmy) 65,137 European ancestry individuals, 431 East Asian ancestry individuals, 1,527 Central Asian ancestry individuals, 186 Hispanic or Latin American individuals, 958 African American or Afro-Caribbean individuals, 261 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Affymetrix [22297997] (imputed) 20 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268467 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:AC case-only heteroplasmy) 813 European ancestry individuals NA Affymetrix [8729006] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268468 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:955:A:AC case-only heteroplasmy) 726 European ancestry individuals NA Affymetrix [8543697] (imputed) 2 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268469 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16093:T:C case-only heteroplasmy) 1,145 European ancestry individuals NA Affymetrix [9283899] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268470 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16129:G:A case-only heteroplasmy) 677 European ancestry individuals NA Affymetrix [8431044] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268471 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16182:A:C case-only heteroplasmy) 1,773 European ancestry individuals, 112 East Asian ancestry individuals, 85 Central Asian ancestry individuals NA Affymetrix [9987702] (imputed) 2 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268472 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16183:A:C case-only heteroplasmy) 5,533 European ancestry individuals, 165 East Asian ancestry individuals, 194 African American or Afro-Caribbean individuals NA Affymetrix [14523372] (imputed) 1 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268473 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16189:T:C case-only heteroplasmy) 493 European ancestry individuals NA Affymetrix [7939759] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268474 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16192:C:T case-only heteroplasmy) 902 European ancestry individuals, 90 African American or Afro-Caribbean individuals NA Affymetrix [8895732] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268475 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:302:A:ACC case-only heteroplasmy) 60,678 European ancestry individuals, 462 East Asian ancestry individuals, 1,379 Central Asian ancestry individuals, 196 Hispanic or Latin American individuals, 813 African American or Afro-Caribbean individuals, 251 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Affymetrix [21835571] (imputed) 8 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268476 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:513:G:GCA case-only heteroplasmy) 1,597 European ancestry individuals NA Affymetrix [9818731] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268477 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:ACC case-only heteroplasmy) 1,480 European ancestry individuals NA Affymetrix [9700250] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268478 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:955:A:ACC case-only heteroplasmy) 733 European ancestry individuals NA Affymetrix [8569132] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268479 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16179:CA:C case-only heteroplasmy) 4,428 European ancestry individuals, 123 Central Asian ancestry individuals, 117 East Asian ancestry individuals, 179 African American or Afro-Caribbean individuals NA Affymetrix [13963351] (imputed) 3 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268480 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16182:A:AC case-only heteroplasmy) 4,511 European ancestry individuals, 188 African American or Afro-Caribbean individuals, 110 Central Asian ancestry individuals, 89 East Asian ancestry individuals NA Affymetrix [11515563] (imputed) 2 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268481 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16183:AC:A case-only heteroplasmy) 6,791 European ancestry individuals, 160 African American or Afro-Caribbean individuals, 111 Central Asian ancestry individuals NA Affymetrix [14210489] (imputed) 6 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268482 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16183:A:AC case-only heteroplasmy) 5,309 European ancestry individuals, 95 Central Asian ancestry individuals NA Affymetrix [11796975] (imputed) 5 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268483 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16192:C:CT case-only heteroplasmy) 524 European ancestry individuals, 73 African American or Afro-Caribbean individuals NA Affymetrix [8034632] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268484 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:302:A:ACCC case-only heteroplasmy) 19,839 European ancestry individuals, 144 African American or Afro-Caribbean individuals, 67 Hispanic or Latin American individuals, 333 Central Asian ancestry individuals, 202 East Asian ancestry individuals, 86 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Affymetrix [15742962] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268485 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:ACCC case-only heteroplasmy) 4,660 European ancestry individuals NA Affymetrix [11570144] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268486 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder 36,301 European ancestry cases, 178,107 European ancestry controls 23,212 European ancestry cases, 151,447 European ancestry controls Affymetrix [723305] (imputed) 4 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90271773 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder 11,920 African ancestry cases, 39,116 African ancestry controls 4,363 African ancestry cases, 10,976 African ancestry controls Affymetrix [723305] (imputed) 10 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90271774 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder 36,301 European ancestry cases, 178,107 European ancestry controls, 11,920 African ancestry cases, 39,116 African ancestry controls 23,212 European ancestry cases, 151,447 European ancestry controls, 4,363 African ancestry cases, 10,976 African ancestry controls Affymetrix [723305] (imputed) 2 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90271775 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder in combat exposure up to 14,520 European ancestry cases, up to 44,527 European ancestry controls NA Affymetrix [723305] (imputed) 10 post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0001358 GCST90271776 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (total) 186,689 European ancestry individuals NA Affymetrix [723305] (imputed) 17 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271777 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (total) up to 51,036 African ancestry individuals NA Affymetrix [723305] (imputed) 0 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271778 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (total) 186,689 European ancestry individuals, up to 51,036 African ancestry individuals NA Affymetrix [723305] (imputed) 16 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271779 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (avoidance) 186,689 European ancestry individuals NA Affymetrix [723305] (imputed) 12 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271780 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (avoidance) 25,414 African ancestry individuals NA Affymetrix [723305] (imputed) 1 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271781 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (avoidance) 186,689 European ancestry individuals, 25,414 African ancestry individuals NA Affymetrix [723305] (imputed) 0 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271782 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (hyperarousal) 186,689 European ancestry individuals NA Affymetrix [723305] (imputed) 19 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271783 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (hyperarousal) 25,521 African ancestry individuals NA Affymetrix [723305] (imputed) 1 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271784 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (hyperarousal) 186,689 European ancestry individuals, 25,521 African ancestry individuals NA Affymetrix [723305] (imputed) 0 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271785 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (re-experiencing) 186,689 European ancestry individuals NA Affymetrix [723305] (imputed) 11 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271786 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (re-experiencing) up to 51,036 African ancestry individuals NA Affymetrix [723305] (imputed) 0 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271787 Genome-wide genotyping array 2023-07-07 33510476 Stein MB 2021-01-28 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33510476 Genome-wide association analyses of post-traumatic stress disorder and its symptom subdomains in the Million Veteran Program. Post-traumatic stress disorder symptom severity (re-experiencing) 186,689 European ancestry individuals, up to 51,036 African ancestry individuals NA Affymetrix [723305] (imputed) 0 post-traumatic stress disorder symptom measurement http://www.ebi.ac.uk/efo/EFO_0008535 GCST90271788 Genome-wide genotyping array 2023-07-11 36921087 Zhou YH 2023-03-15 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/36921087 Genetic Modifiers of Cystic Fibrosis Lung Disease Severity: Whole Genome Analysis of 7,840 Patients. Lung disease severity in cystic fibrosis with pancreatic insufficiency 7,437 European ancestry individuals, 403 individuals NA NR [15900000] (imputed) 77 lung disease severity measurement http://www.ebi.ac.uk/efo/EFO_0007744 GCST90271928 Genome-wide genotyping array, Genome-wide sequencing 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16179:CAA:C case-only heteroplasmy) 1,687 European ancestry individuals, 83 Central Asian ancestry individuals, 104 East Asian ancestry individuals NA Affymetrix [10079834] (imputed) 3 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268487 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16182:A:ACC case-only heteroplasmy) 3,523 European ancestry individuals, 144 African American or Afro-Caribbean individuals, 87 Central Asian ancestry individuals, 75 East Asian ancestry individuals NA Affymetrix [13074752] (imputed) 4 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268488 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16183:A:ACC case-only heteroplasmy) 4,607 European ancestry individuals, 113 African American or Afro-Caribbean individuals NA Affymetrix [12902939] (imputed) 4 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268489 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:302:A:ACCCC case-only heteroplasmy) 2,377 European ancestry individuals, 66 Central Asian ancestry individuals, 77 East Asian ancestry individuals NA Affymetrix [10470770] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268490 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:ACCCC case-only heteroplasmy) 5,399 European ancestry individuals, 107 Central Asian ancestry individuals NA Affymetrix [11825139] (imputed) 1 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268491 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16183:A:ACCC case-only heteroplasmy) 1,734 European ancestry individuals, 83 Central Asian ancestry individuals, 103 East Asian ancestry individuals NA Affymetrix [10118698] (imputed) 0 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268492 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:ACCCCC case-only heteroplasmy) 4,906 European ancestry individuals, 99 Central Asian ancestry individuals NA Affymetrix [11665233] (imputed) 1 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268493 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:16183:A:ACCCC case-only heteroplasmy) 1,492 European ancestry individuals, 71 Central Asian ancestry individuals, 94 East Asian ancestry individuals NA Affymetrix [9863118] (imputed) 2 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268494 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:ACCCCCC case-only heteroplasmy) 4,122 European ancestry individuals NA Affymetrix [11366361] (imputed) 3 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268495 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA heteroplasmy (chrM:567:A:ACCCCCCC case-only heteroplasmy) 1,738 European ancestry individuals NA Affymetrix [9957089] (imputed) 1 mitochondrial heteroplasmy measurement http://www.ebi.ac.uk/efo/EFO_0600008 GCST90268496 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA copy number (adjusted) 155,998 European ancestry individuals, 2,138 African American or Afro-Caribbean individuals, 381 Hispanic or Latin American individuals, 3,326 Central Asian ancestry individuals, 958 East Asian ancestry individuals, 571 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Affymetrix [24575117] (imputed) 92 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90268497 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA copy number (raw) 155,998 European ancestry individuals, 2,138 African American or Afro-Caribbean individuals, 381 Hispanic or Latin American individuals, 3,326 Central Asian ancestry individuals, 958 East Asian ancestry individuals, 571 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Affymetrix [24575117] (imputed) 141 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90268498 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA coverage discrepancy (between 7s DNA region and DNA flap region) 124,714 European ancestry individuals, 729 East Asian ancestry individuals, 2,540 Central Asian ancestry individuals, 313 Hispanic or Latin American individuals, 1,895 African American or Afro-Caribbean individuals, 467 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Affymetrix [24222815] (imputed) 0 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90268499 Genome-wide genotyping array 2023-08-30 37587338 Gupta R 2023-08-16 Nature www.ncbi.nlm.nih.gov/pubmed/37587338 Nuclear genetic control of mtDNA copy number and heteroplasmy in humans. Mitochondrial DNA coverage discrepancy (between RNA primer region and DNA flap region) 124,714 European ancestry individuals, 729 East Asian ancestry individuals, 2,540 Central Asian ancestry individuals, 313 Hispanic or Latin American individuals, 1,895 African American or Afro-Caribbean individuals, 467 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals NA Affymetrix [24222815] (imputed) 0 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90268500 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Tyrosine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90292783 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Acetate levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90292784 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. 3-Hydroxybutyrate levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90292785 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Creatine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90292786 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Albumin (signal area) levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90292787 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycoprotein acetyls levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90292788 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very very large VLDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292789 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90292790 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90292791 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292792 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292793 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292794 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292795 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very large VLDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292796 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 total lipids in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022313 GCST90292797 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292798 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292799 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292800 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 free cholesterol in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022274 GCST90292801 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 triglycerides in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022325 GCST90292802 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large VLDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292803 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 total lipids in large VLDL http://www.ebi.ac.uk/efo/EFO_0022175 GCST90292804 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292805 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 total cholesterol in large VLDL http://www.ebi.ac.uk/efo/EFO_0022177 GCST90292806 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 free cholesterol in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022265 GCST90292808 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 triglycerides in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022178 GCST90292809 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium VLDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292810 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 17 total lipids in medium VLDL http://www.ebi.ac.uk/efo/EFO_0022153 GCST90292811 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292812 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in medium VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 total cholesterol in medium VLDL http://www.ebi.ac.uk/efo/EFO_0022162 GCST90292813 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 18 cholesterol esters in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022182 GCST90292814 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 15 free cholesterol in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022269 GCST90292815 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 13 triglycerides in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022155 GCST90292816 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small VLDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292817 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 total lipids in small VLDL http://www.ebi.ac.uk/efo/EFO_0022148 GCST90292818 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292819 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total cholesterol in small VLDL http://www.ebi.ac.uk/efo/EFO_0022171 GCST90292820 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292821 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 free cholesterol in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022272 GCST90292822 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 25 triglycerides in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022145 GCST90292823 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very small VLDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292824 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 total lipids in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022156 GCST90292825 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292826 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 cholesterol esters in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022170 GCST90292807 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022231 GCST90292827 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292828 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 free cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022275 GCST90292829 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very small VLDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 triglycerides in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022144 GCST90292830 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of IDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90292831 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in IDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 total lipids in IDL http://www.ebi.ac.uk/efo/EFO_0022161 GCST90292832 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022321 GCST90292733 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small HDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292734 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 total lipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022311 GCST90292735 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022296 GCST90292736 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in small HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292737 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292738 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 free cholesterol in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022270 GCST90292739 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022158 GCST90292740 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of VLDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 3 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90292741 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of LDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90292742 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of HDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90292743 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Serum total cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90292744 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. VLDL cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292745 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Remnant cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 remnant cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010815 GCST90292746 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. LDL cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292747 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292748 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL2 cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292749 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL3 cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292750 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total esterified cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292751 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90292752 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total triglycerides levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90292753 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. VLDL triglycerides levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292754 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. LDL triglycerides levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglyceride measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292755 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL triglycerides levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292756 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total phosphoglycerides levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 phosphoglycerides measurement http://www.ebi.ac.uk/efo/EFO_0022291 GCST90292757 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 triglycerides in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022323 GCST90292858 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very large HDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292859 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 total lipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022312 GCST90292860 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 phospholipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022298 GCST90292861 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in very large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292862 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292863 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 free cholesterol in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022273 GCST90292864 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 triglycerides in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022324 GCST90292865 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large HDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 8 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292866 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 8 total lipids in large HDL http://www.ebi.ac.uk/efo/EFO_0022189 GCST90292867 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 7 phospholipids in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022190 GCST90292868 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 6 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292869 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 cholesterol esters in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022159 GCST90292870 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 free cholesterol in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022157 GCST90292871 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 triglycerides in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022318 GCST90292872 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium HDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292873 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 total lipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022310 GCST90292874 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 phospholipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022295 GCST90292875 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in medium HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292876 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292877 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 free cholesterol in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022267 GCST90292878 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 triglycerides in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022321 GCST90292879 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small HDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292880 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total lipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022311 GCST90292881 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 phospholipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022296 GCST90292882 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022297 GCST90292708 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in small LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 total cholesterol in small LDL http://www.ebi.ac.uk/efo/EFO_0022179 GCST90292709 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292710 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022271 GCST90292711 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022323 GCST90292712 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very large HDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292713 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 3 total lipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022312 GCST90292714 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 phospholipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022298 GCST90292715 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in very large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292716 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292717 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022273 GCST90292718 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 triglycerides in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022324 GCST90292719 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large HDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292720 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in large HDL http://www.ebi.ac.uk/efo/EFO_0022189 GCST90292721 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 phospholipids in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022190 GCST90292722 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292723 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 cholesterol esters in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022159 GCST90292724 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022157 GCST90292725 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022318 GCST90292726 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium HDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292727 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 total lipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022310 GCST90292728 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 phospholipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022295 GCST90292729 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in medium HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292730 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292731 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium HDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022267 GCST90292732 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phosphatidylcholine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90292758 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Sphingomyelins levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90292759 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholines levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90292760 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Apolipoprotein A1 levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90292761 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Apolipoprotein B levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90292762 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total fatty acids 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90292763 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Docosahexaenoic acid (22:6) levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90292764 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Linoleic acid (18:2) levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90292765 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Omega-3 fatty acids levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90292766 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Omega-6 fatty acids levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90292767 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Polyunsaturated fatty acids 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST90292768 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Monounsaturated fatty acids 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90292769 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Saturated fatty acids 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 saturated fatty acids measurement http://www.ebi.ac.uk/efo/EFO_0022304 GCST90292770 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Lactate levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90292771 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Pyruvate levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90292772 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Citrate levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 4 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90292773 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycerol levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90292774 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Alanine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90292775 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glutamine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90292776 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90292777 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Histidine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90292778 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Isoleucine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90292779 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Leucine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90292780 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Valine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90292781 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phenylalanine levels 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90292782 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in IDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 phospholipids in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022164 GCST90292833 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in IDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total cholesterol in IDL http://www.ebi.ac.uk/efo/EFO_0022184 GCST90292834 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in IDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 esterified cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90292835 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in IDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022181 GCST90292836 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in IDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 triglycerides in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022149 GCST90292837 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large LDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292838 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 total lipids in large LDL http://www.ebi.ac.uk/efo/EFO_0022163 GCST90292839 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 phospholipids in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022174 GCST90292840 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in large LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total cholesterol in large LDL http://www.ebi.ac.uk/efo/EFO_0022167 GCST90292841 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 cholesterol esters in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022165 GCST90292842 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022176 GCST90292843 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 triglycerides in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022319 GCST90292844 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium LDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292845 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium LDL-L 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 total lipids in medium LDL http://www.ebi.ac.uk/efo/EFO_0022180 GCST90292846 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 phospholipids in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022183 GCST90292847 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in medium LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total cholesterol in medium LDL http://www.ebi.ac.uk/efo/EFO_0022185 GCST90292848 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 cholesterol esters in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022186 GCST90292849 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 free cholesterol in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022268 GCST90292850 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 triglycerides in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022322 GCST90292851 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small LDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292852 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 total lipids in small LDL http://www.ebi.ac.uk/efo/EFO_0022168 GCST90292853 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 phospholipids in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022297 GCST90292854 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in small LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 total cholesterol in small LDL http://www.ebi.ac.uk/efo/EFO_0022179 GCST90292855 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292856 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small LDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 free cholesterol in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022271 GCST90292857 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Albumin (signal area) levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90292933 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycoprotein acetyls levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90292934 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very very large VLDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 6 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292935 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90292936 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90292937 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292938 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292939 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292940 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292941 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very large VLDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 7 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292942 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 total lipids in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022313 GCST90292943 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292944 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292945 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 7 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292946 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 8 free cholesterol in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022274 GCST90292947 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 triglycerides in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022325 GCST90292948 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large VLDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292949 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 total lipids in large VLDL http://www.ebi.ac.uk/efo/EFO_0022175 GCST90292950 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 7 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292951 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 7 total cholesterol in large VLDL http://www.ebi.ac.uk/efo/EFO_0022177 GCST90292952 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 cholesterol esters in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022170 GCST90292953 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 free cholesterol in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022265 GCST90292954 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 triglycerides in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022178 GCST90292955 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium VLDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292956 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 56 total lipids in medium VLDL http://www.ebi.ac.uk/efo/EFO_0022153 GCST90292957 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in small HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292883 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292884 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 free cholesterol in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022270 GCST90292885 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small HDL 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 triglycerides in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022158 GCST90292886 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of VLDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90292887 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of LDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90292888 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of HDL particles 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90292889 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Serum total cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90292890 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. VLDL cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292891 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Remnant cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 remnant cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010815 GCST90292892 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. LDL cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292893 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 6 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292894 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL2 cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292895 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL3 cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292896 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total esterified cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292897 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90292898 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total triglycerides levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90292899 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. VLDL triglycerides levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292900 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. LDL triglycerides levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 triglyceride measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292901 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL triglycerides levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292902 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total phosphoglycerides levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 phosphoglycerides measurement http://www.ebi.ac.uk/efo/EFO_0022291 GCST90292903 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phosphatidylcholine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90292904 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Sphingomyelins levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90292905 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholines levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90292906 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Apolipoprotein A1 levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 7 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90292907 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292958 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in medium VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 total cholesterol in medium VLDL http://www.ebi.ac.uk/efo/EFO_0022162 GCST90292959 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 8 cholesterol esters in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022182 GCST90292960 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 40 free cholesterol in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022269 GCST90292961 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 38 triglycerides in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022155 GCST90292962 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small VLDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 5 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292963 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 4 total lipids in small VLDL http://www.ebi.ac.uk/efo/EFO_0022148 GCST90292964 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 4 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292965 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 total cholesterol in small VLDL http://www.ebi.ac.uk/efo/EFO_0022171 GCST90292966 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292967 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 free cholesterol in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022272 GCST90292968 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 triglycerides in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022145 GCST90292969 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very small VLDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 8 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292970 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 total lipids in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022156 GCST90292971 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292972 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 8 cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022231 GCST90292973 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292974 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 11 free cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022275 GCST90292975 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very small VLDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 triglycerides in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022144 GCST90292976 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of IDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 4 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90292977 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in IDL 3,354 European ancestry individuals NA NR [NR] (imputed) 4 total lipids in IDL http://www.ebi.ac.uk/efo/EFO_0022161 GCST90292978 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in IDL 3,354 European ancestry individuals NA NR [NR] (imputed) 3 phospholipids in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022164 GCST90292979 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in IDL 3,354 European ancestry individuals NA NR [NR] (imputed) 3 total cholesterol in IDL http://www.ebi.ac.uk/efo/EFO_0022184 GCST90292980 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in IDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 esterified cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90292981 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in IDL 3,354 European ancestry individuals NA NR [NR] (imputed) 1 free cholesterol in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022181 GCST90292982 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Apolipoprotein B levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90292908 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total fatty acids 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90292909 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Docosahexaenoic acid (22:6) levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90292910 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Linoleic acid (18:2) levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90292911 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Omega-3 fatty acids levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90292912 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Omega-6 fatty acids levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90292913 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Polyunsaturated fatty acids 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST90292914 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Monounsaturated fatty acids 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90292915 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Saturated fatty acids 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 saturated fatty acids measurement http://www.ebi.ac.uk/efo/EFO_0022304 GCST90292916 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Lactate levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90292917 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Pyruvate levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90292918 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Citrate levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 6 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90292919 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycerol levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90292920 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Alanine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90292921 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glutamine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90292922 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90292923 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Histidine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 5 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90292924 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Isoleucine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90292925 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Leucine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 1 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90292926 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Valine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 3 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90292927 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phenylalanine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90292928 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Tyrosine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 2 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90292929 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Acetate levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 4 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90292930 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. 3-Hydroxybutyrate levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90292931 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Creatine levels 3,688 South Asian ancestry individuals NA NR [NR] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90292932 Genome-wide genotyping array 2023-08-24 37216007 Allaire P 2023-04-27 HGG Adv www.ncbi.nlm.nih.gov/pubmed/37216007 Genetic and clinical determinants of telomere length. Leukocyte telomere length 62,271 European ancestry individuals NA Illumina [7407505] 44 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90278198 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of VLDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 9 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90293033 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of LDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 6 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90293034 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Mean diameter of HDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 15 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90293035 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Serum total cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 6 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90293036 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. VLDL cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 4 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90293037 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Remnant cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 10 remnant cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0010815 GCST90293038 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. LDL cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 4 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90293039 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293040 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL2 cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 9 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293041 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL3 cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 8 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293042 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total esterified cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 5 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90293043 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 4 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90293044 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total triglycerides levels 3,354 European ancestry individuals NA NR [NR] (imputed) 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90293045 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. VLDL triglycerides levels 3,354 European ancestry individuals NA NR [NR] (imputed) 7 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90293046 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. LDL triglycerides levels 3,354 European ancestry individuals NA NR [NR] (imputed) 7 triglyceride measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90293047 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. HDL triglycerides levels 3,354 European ancestry individuals NA NR [NR] (imputed) 13 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293048 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total phosphoglycerides levels 3,354 European ancestry individuals NA NR [NR] (imputed) 7 phosphoglycerides measurement http://www.ebi.ac.uk/efo/EFO_0022291 GCST90293049 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phosphatidylcholine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 10 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90293050 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Sphingomyelins levels 3,354 European ancestry individuals NA NR [NR] (imputed) 7 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90293051 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholines levels 3,354 European ancestry individuals NA NR [NR] (imputed) 8 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90293052 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Apolipoprotein A1 levels 3,354 European ancestry individuals NA NR [NR] (imputed) 13 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90293053 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Apolipoprotein B levels 3,354 European ancestry individuals NA NR [NR] (imputed) 7 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90293054 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total fatty acids 3,354 European ancestry individuals NA NR [NR] (imputed) 8 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90293055 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Docosahexaenoic acid (22:6) levels 3,354 European ancestry individuals NA NR [NR] (imputed) 7 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90293056 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Linoleic acid (18:2) levels 3,354 European ancestry individuals NA NR [NR] (imputed) 8 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90293057 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in very large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 13 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293008 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293009 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 free cholesterol in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022273 GCST90293010 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 7 triglycerides in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022324 GCST90293011 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large HDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 13 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293012 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 total lipids in large HDL http://www.ebi.ac.uk/efo/EFO_0022189 GCST90293013 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 8 phospholipids in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022190 GCST90293014 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 13 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293015 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 cholesterol esters in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022159 GCST90293016 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 13 free cholesterol in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022157 GCST90293017 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 11 triglycerides in large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022318 GCST90293018 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium HDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 11 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293019 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 total lipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022310 GCST90293020 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 9 phospholipids in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022295 GCST90293021 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in medium HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293022 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 13 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293023 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 free cholesterol in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022267 GCST90293024 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 7 triglycerides in medium HDL measurement http://www.ebi.ac.uk/efo/EFO_0022321 GCST90293025 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small HDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 11 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293026 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 total lipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022311 GCST90293027 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 15 phospholipids in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022296 GCST90293028 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol levels in small HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293029 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293030 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 12 free cholesterol in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022270 GCST90293031 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 7 triglycerides in small HDL measurement http://www.ebi.ac.uk/efo/EFO_0022158 GCST90293032 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in IDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 triglycerides in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022149 GCST90292983 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large LDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 5 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292984 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 total lipids in large LDL http://www.ebi.ac.uk/efo/EFO_0022163 GCST90292985 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 phospholipids in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022174 GCST90292986 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in large LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 total cholesterol in large LDL http://www.ebi.ac.uk/efo/EFO_0022167 GCST90292987 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 4 cholesterol esters in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022165 GCST90292988 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 2 free cholesterol in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022176 GCST90292989 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 8 triglycerides in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022319 GCST90292990 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium LDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 4 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292991 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium LDL-L 3,354 European ancestry individuals NA NR [NR] (imputed) 3 total lipids in medium LDL http://www.ebi.ac.uk/efo/EFO_0022180 GCST90292992 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 3 phospholipids in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022183 GCST90292993 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in medium LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 4 total cholesterol in medium LDL http://www.ebi.ac.uk/efo/EFO_0022185 GCST90292994 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 4 cholesterol esters in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022186 GCST90292995 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 free cholesterol in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022268 GCST90292996 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 triglycerides in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022322 GCST90292997 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small LDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 6 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292998 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 total lipids in small LDL http://www.ebi.ac.uk/efo/EFO_0022168 GCST90292999 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 phospholipids in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022297 GCST90293000 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in small LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 6 total cholesterol in small LDL http://www.ebi.ac.uk/efo/EFO_0022179 GCST90293001 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 5 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90293002 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 7 free cholesterol in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022271 GCST90293003 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small LDL 3,354 European ancestry individuals NA NR [NR] (imputed) 13 triglycerides in small LDL measurement http://www.ebi.ac.uk/efo/EFO_0022323 GCST90293004 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very large HDL particles 3,354 European ancestry individuals NA NR [NR] (imputed) 11 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90293005 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 11 total lipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022312 GCST90293006 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very large HDL 3,354 European ancestry individuals NA NR [NR] (imputed) 10 phospholipids in very large HDL measurement http://www.ebi.ac.uk/efo/EFO_0022298 GCST90293007 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90292645 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292646 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292647 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292648 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292649 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very large VLDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292650 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022313 GCST90292651 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292652 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292653 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292654 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 free cholesterol in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022274 GCST90292655 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in very large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022325 GCST90292656 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large VLDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292657 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in large VLDL http://www.ebi.ac.uk/efo/EFO_0022175 GCST90292658 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292659 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol in large VLDL http://www.ebi.ac.uk/efo/EFO_0022177 GCST90292660 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 cholesterol esters in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022170 GCST90292661 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022265 GCST90292662 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in large VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022178 GCST90292663 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium VLDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292664 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 4 total lipids in medium VLDL http://www.ebi.ac.uk/efo/EFO_0022153 GCST90292665 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292666 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in medium VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol in medium VLDL http://www.ebi.ac.uk/efo/EFO_0022162 GCST90292667 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 cholesterol esters in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022182 GCST90292668 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 free cholesterol in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022269 GCST90292669 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 2 triglycerides in medium VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022155 GCST90292670 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small VLDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292671 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in small VLDL http://www.ebi.ac.uk/efo/EFO_0022148 GCST90292672 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292673 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol in small VLDL http://www.ebi.ac.uk/efo/EFO_0022171 GCST90292674 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292675 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022272 GCST90292676 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 triglycerides in small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022145 GCST90292677 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very small VLDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292678 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022156 GCST90292679 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in very small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022301 GCST90292680 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in very small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022231 GCST90292681 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in very small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90292682 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in very small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022275 GCST90292683 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in very small VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in very small VLDL measurement http://www.ebi.ac.uk/efo/EFO_0022144 GCST90292684 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of IDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90292685 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in IDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in IDL http://www.ebi.ac.uk/efo/EFO_0022161 GCST90292686 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in IDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022164 GCST90292687 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total Cholesterol in IDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol in IDL http://www.ebi.ac.uk/efo/EFO_0022184 GCST90292688 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in IDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 esterified cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90292689 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in IDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022181 GCST90292690 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in IDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in IDL measurement http://www.ebi.ac.uk/efo/EFO_0022149 GCST90292691 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of large LDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292692 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in large LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in large LDL http://www.ebi.ac.uk/efo/EFO_0022163 GCST90292693 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in large LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022174 GCST90292694 Genome-wide genotyping array 2023-07-05 36902448 Mori Y 2023-03-06 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/36902448 Genome-Wide Association Study and Transcriptome of Japanese Patients with Developmental Dysplasia of the Hip Demonstrates an Association with the Ferroptosis Signaling Pathway. Developmental dysplasia of the hip 238 Japanese ancestry cases, 2,044 Japanese ancestry controls 3,315 European ancestry cases, 74,038 European ancestry controls NR [659253] (imputed) 7 developmental dysplasia of the hip http://www.ebi.ac.uk/efo/EFO_1000648 GCST90271727 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Omega-6 fatty acids levels 3,354 European ancestry individuals NA NR [NR] (imputed) 6 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90293059 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Polyunsaturated fatty acids 3,354 European ancestry individuals NA NR [NR] (imputed) 9 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010733 GCST90293060 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Monounsaturated fatty acids 3,354 European ancestry individuals NA NR [NR] (imputed) 12 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90293061 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Saturated fatty acids 3,354 European ancestry individuals NA NR [NR] (imputed) 6 saturated fatty acids measurement http://www.ebi.ac.uk/efo/EFO_0022304 GCST90293062 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Lactate levels 3,354 European ancestry individuals NA NR [NR] (imputed) 7 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90293063 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Pyruvate levels 3,354 European ancestry individuals NA NR [NR] (imputed) 4 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90293064 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Citrate levels 3,354 European ancestry individuals NA NR [NR] (imputed) 16 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90293065 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycerol levels 3,354 European ancestry individuals NA NR [NR] (imputed) 8 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90293066 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Alanine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 16 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90293067 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glutamine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 4 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90293068 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 8 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90293069 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Histidine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 8 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90293070 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Isoleucine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 6 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90293071 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Leucine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 10 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90293072 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Valine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 5 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90293073 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phenylalanine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 3 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90293074 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Tyrosine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 5 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90293075 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Acetate levels 3,354 European ancestry individuals NA NR [NR] (imputed) 6 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90293076 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. 3-Hydroxybutyrate levels 3,354 European ancestry individuals NA NR [NR] (imputed) 6 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90293077 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Creatine levels 3,354 European ancestry individuals NA NR [NR] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90293078 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Albumin (signal area) levels 3,354 European ancestry individuals NA NR [NR] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90293079 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Glycoprotein acetyls levels 3,354 European ancestry individuals NA NR [NR] (imputed) 0 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90293080 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of very very large VLDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90292643 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in very very large VLDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90292644 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in large LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol in large LDL http://www.ebi.ac.uk/efo/EFO_0022167 GCST90292695 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in large LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 cholesterol esters in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022165 GCST90292696 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in large LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 1 free cholesterol in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022176 GCST90292697 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in large LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in large LDL measurement http://www.ebi.ac.uk/efo/EFO_0022319 GCST90292698 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of medium LDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292699 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in medium LDL-L 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in medium LDL http://www.ebi.ac.uk/efo/EFO_0022180 GCST90292700 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Phospholipids in medium LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 phospholipids in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022183 GCST90292701 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total cholesterol in medium LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total cholesterol in medium LDL http://www.ebi.ac.uk/efo/EFO_0022185 GCST90292702 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Cholesterol esters in medium LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 cholesterol esters in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022186 GCST90292703 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Free cholesterol in medium LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 free cholesterol in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022268 GCST90292704 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Triglycerides in medium LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 triglycerides in medium LDL measurement http://www.ebi.ac.uk/efo/EFO_0022322 GCST90292705 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Concentration of small LDL particles 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90292706 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Total lipids in small LDL 3,688 South Asian ancestry individuals, 3,354 European ancestry individuals NA NR [NR] (imputed) 0 total lipids in small LDL http://www.ebi.ac.uk/efo/EFO_0022168 GCST90292707 Genome-wide genotyping array 2023-06-30 36747475 Aegisdottir HM 2023-02-07 Eur Heart J www.ncbi.nlm.nih.gov/pubmed/36747475 Genetic variants associated with syncope implicate neural and autonomic processes. Syncope 56,071 European ancestry cases, 890,790 European ancestry controls 22,412 European ancestry cases, 286,003 European ancestry controls Affymetrix, Illumina [61830718] 3 Syncope http://purl.obolibrary.org/obo/HP_0001279 GCST90271681 Genome-wide genotyping array, Genome-wide sequencing 2023-07-05 37334860 Moscati A 2023-06-19 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37334860 Life is pain: Fibromyalgia as a nexus of multiple liability distributions. Fibromyalgia 280 African or African American cases, 14,860 African or African American controls NA Illumina [16720666] (imputed) 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90091913 Genome-wide genotyping array 2023-07-05 37334860 Moscati A 2023-06-19 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37334860 Life is pain: Fibromyalgia as a nexus of multiple liability distributions. Fibromyalgia 1,362 European ancestry cases, 44,047 European ancestry controls NA Illumina [9879997] (imputed) 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90091914 Genome-wide genotyping array 2023-07-05 37334860 Moscati A 2023-06-19 Am J Med Genet B Neuropsychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37334860 Life is pain: Fibromyalgia as a nexus of multiple liability distributions. Fibromyalgia 1,642 African, African American or European ancestry cases, 58,907 African, African American or European ancestry controls NA Illumina [18126921] (imputed) 0 fibromyalgia http://www.ebi.ac.uk/efo/EFO_0005687 GCST90091915 Genome-wide genotyping array 2023-10-05 37255970 Fuller H 2023-05-15 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37255970 Metabolic drivers of dysglycemia in pregnancy: ethnic-specific GWAS of 146 metabolites and 1-sample Mendelian randomization analyses in a UK multi-ethnic birth cohort. Omega-3 fatty acids levels 3,354 European ancestry individuals NA NR [NR] (imputed) 4 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90293058 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Feeling anxious - several or more days in the last two weeks 40,282 European ancestry cases, 98,623 European ancestry controls NA NR [7749106] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90225516 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Feeling of foreboding - several or more days in the last two weeks 23,589 European ancestry cases, 115,171 European ancestry controls NA NR [7749106] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90225517 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Inability to control worry - several or more days in the last two weeks 33,331 European ancestry cases, 105,549 European ancestry controls NA NR [7749106] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90225518 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Easily annoyed or irritable - several or more days in the last two weeks 38,854 European ancestry cases, 99,911 European ancestry controls NA NR [7749106] (imputed) 0 irritability measurement http://www.ebi.ac.uk/efo/EFO_0009594 GCST90225519 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Being restless - several or more days in the last two weeks 16,693 European ancestry cases, 122,416 European ancestry controls NA NR [7749106] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90225520 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Trouble relaxing - several or more days in the last two weeks 40,314 European ancestry cases, 98,699 European ancestry controls NA NR [7749106] (imputed) 0 feeling tense measurement http://www.ebi.ac.uk/efo/EFO_0009596 GCST90225521 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Worrying too much - several or more days in the last two weeks 44,438 European ancestry cases, 94,432 European ancestry controls NA NR [7749106] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90225522 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. Generalized anxiety disorder sum score 139,363 European ancestry individuals NA NR [7749106] (imputed) 0 anxiety disorder measurement http://www.ebi.ac.uk/efo/EFO_0007795 GCST90225523 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. ICD10 F40.2: Specific (isolated) phobias 1,809 European ancestry cases, 500,672 European ancestry controls NA NR [7749106] (imputed) 0 phobic disorder http://www.ebi.ac.uk/efo/EFO_1001908 GCST90225524 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. ICD10 F41.0: Panic disorder [episodic paroxysmal anxiety] 1,909 European ancestry cases, 500,553 European ancestry controls NA NR [7749106] (imputed) 0 panic disorder http://www.ebi.ac.uk/efo/EFO_0004262 GCST90225525 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. ICD10 F41.2: Mixed anxiety and depressive disorder 3,769 European ancestry cases, 498,711 European ancestry controls NA NR [7749106] (imputed) 0 mixed anxiety and depressive disorder http://purl.obolibrary.org/obo/MONDO_0041086 GCST90225526 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. ICD10 F41.9: Anxiety disorder, unspecified 16,079 European ancestry cases, 486,398 European ancestry controls NA NR [7749106] (imputed) 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90225527 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. ICD10 F40 F41 F42: any anxiety disorder 21,606 European ancestry cases, 480,868 European ancestry controls NA NR [7749106] (imputed) 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90225528 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. ICD10 F41: Other anxiety disorders 19,596 European ancestry cases, 482,872 European ancestry controls NA NR [7749106] (imputed) 0 anxiety disorder http://www.ebi.ac.uk/efo/EFO_0006788 GCST90225529 Genome-wide genotyping array 2023-08-30 37259642 Brasher MS 2023-05-31 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/37259642 Testing associations between human anxiety and genes previously implicated by mouse anxiety models. ICD10 F40: Phobic anxiety disorders 2,060 European ancestry cases, 500,421 European ancestry controls NA NR [7749106] (imputed) 0 phobic disorder http://www.ebi.ac.uk/efo/EFO_1001908 GCST90225530 Genome-wide genotyping array 2023-08-08 37017090 Yu M 2023-04-05 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/37017090 Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. Interventricular septum cross-sectional area 306 African or Afro-Caribbean individuals NA NR [NR] (imputed) 3 interventricular septum thickness http://www.ebi.ac.uk/efo/EFO_0009287 GCST90275231 Genome-wide genotyping array 2023-08-08 37017090 Yu M 2023-04-05 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/37017090 Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. Interventricular septum cross-sectional area 90 South Asian ancestry individuals NA NR [NR] (imputed) 3 interventricular septum thickness http://www.ebi.ac.uk/efo/EFO_0009287 GCST90275232 Genome-wide genotyping array 2023-08-08 37017090 Yu M 2023-04-05 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/37017090 Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. Interventricular septum cross-sectional area 29,975 European ancestry individuals, 306 African or Afro-Caribbean individuals, 90 South Asian ancestry individuals, 395 East Asian ancestry individuals NA NR [NR] (imputed) 7 interventricular septum thickness http://www.ebi.ac.uk/efo/EFO_0009287 GCST90275230 Genome-wide genotyping array 2023-08-08 37017090 Yu M 2023-04-05 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/37017090 Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic Cardiomyopathy. Interventricular septum cross-sectional area 395 East Asian ancestry individuals NA NR [NR] (imputed) 3 interventricular septum thickness http://www.ebi.ac.uk/efo/EFO_0009287 GCST90275233 Genome-wide genotyping array 2023-08-08 37031923 Benca-Bachman CE 2023-04-07 Mol Cell Neurosci www.ncbi.nlm.nih.gov/pubmed/37031923 Polygenic influences on the behavioral effects of alcohol withdrawal in a mixed-ancestry population from the collaborative study on the genetics of alcoholism (COGA). Alcohol withdrawal factor score 8,009 European, African or unknown ancestry individuals from families NA Illumina [2665312] (imputed) 19 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90275372 Genome-wide genotyping array 2023-06-21 36835855 Xiao Q 2023-02-07 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36835855 Establishing a Prediction Model for the Efficacy of Platinum-Based Chemotherapy in NSCLC Based on a Two Cohorts GWAS Study. Response to platinum-based chemotherapy in non-small-cell lung cancer 104 East Asian ancestry responders, 113 East Asian ancestry non-responders NA Illumina [6294406] (imputed) 0 response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0004647 GCST90270937 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea 5,438 Han Chinese ancestry cases, 15,152 Han Chinese ancestry controls NA Affymetrix [4339910] (imputed) 5 obstructive sleep apnea http://www.ebi.ac.uk/efo/EFO_0003918 GCST90258599 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Apnea hypopnea index 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 2 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258600 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Apnea hypopnea index during non-REM sleep 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 2 sleep apnea measurement during non-REM sleep http://www.ebi.ac.uk/efo/EFO_0008456 GCST90258601 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Apnea hypopnea index during REM sleep 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement during REM sleep http://www.ebi.ac.uk/efo/EFO_0008455 GCST90258602 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Non-supine apnea hypopnea index 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 3 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258603 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Supine apnea hypopnea index 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258604 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive apnea hypopnea index 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258605 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Longest duration of obstructive apnea or hypopnea events 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258606 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (percentage of blood oxygen below 90% of total sleep time) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258607 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (oxygen desaturation index) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258608 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (average oxyhemoglobin saturation across sleep episode) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258609 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (minimum oxyhemoglobin saturation across sleep episode) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 2 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258610 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (micro-arousal index) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258611 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (wake time during sleep period time) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258612 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (percentage of wake time during sleep period time) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 4 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258613 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (percentage of rapid eye movement during sleep period time) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258614 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (percentage of rapid eye movement during total sleep time) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258615 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (percentage of N3 sleep time during sleep period time) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 0 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258616 Genome-wide genotyping array 2023-03-21 35819321 Xu H 2022-07-12 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/35819321 Genome-Wide Association Study of Obstructive Sleep Apnea and Objective Sleep-Related Traits Identifies Novel Risk Loci in Han Chinese Individuals. Obstructive sleep apnea trait (percentage of N3 sleep time during total sleep time) 6,246 Han Chinese ancestry individuals NA Affymetrix [4339910] (imputed) 1 sleep apnea measurement http://www.ebi.ac.uk/efo/EFO_0007817 GCST90258617 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Waist-to-hip ratio adjusted for BMI 186,825 British ancestry men NA Affymetrix [323858] (imputed) 571 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST012230 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Hip index 186,825 British ancestry men NA Affymetrix [323858] (imputed) 222 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST012229 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Waist-hip index 186,825 British ancestry men NA Affymetrix [127266] (imputed) 617 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST012228 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Waist circumference adjusted for body mass index 186,825 British ancestry men NA Affymetrix [321114] (imputed) 842 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST012226 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. A body shape index 219,872 British ancestry women NA Affymetrix [321169] (imputed) 1273 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90020024 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Waist-to-hip ratio adjusted for BMI 219,872 British ancestry women NA Affymetrix [319769] (imputed) 1959 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90020025 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Hip index 219,872 British ancestry women NA Affymetrix [321788] (imputed) 814 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST90020026 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Waist-hip index 219,872 British ancestry women NA Affymetrix [319769] (imputed) 1988 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90020027 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Hip circumference adjusted for BMI 219,872 British ancestry women NA Affymetrix [321016] (imputed) 2008 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST90020028 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Waist circumference adjusted for body mass index 219,872 British ancestry women NA Affymetrix [321114] (imputed) 1586 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90020029 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. A body shape index 186,825 British ancestry men NA Affymetrix [323858] (imputed) 266 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST012231 Genome-wide genotyping array 2021-08-24 34021172 Christakoudi S 2021-05-21 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34021172 GWAS of allometric body-shape indices in UK Biobank identifies loci suggesting associations with morphogenesis, organogenesis, adrenal cell renewal and cancer. Hip circumference adjusted for BMI 186,825 British ancestry men NA Affymetrix [323123] (imputed) 1400 BMI-adjusted hip circumference http://www.ebi.ac.uk/efo/EFO_0008039 GCST012227 Genome-wide genotyping array 2023-03-07 36804072 Pardinas AF 2023-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/36804072 Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data. Plasma clozapine levels in treatment-resistant schizophrenia 3,677 European ancestry individuals, 243 Sub-Saharan African ancestry individuals, 122 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals, 244 South Asian ancestry individuals, 41 East Asian ancestry individuals, 168 NR ancestry, Other admixed ancestry individuals NA Illumina [2906712] (imputed) 2 plasma clozapine measurement http://www.ebi.ac.uk/efo/EFO_0600038 GCST90239836 Genome-wide genotyping array 2023-03-07 36804072 Pardinas AF 2023-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/36804072 Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data. Plasma norclozapine levels in treatment-resistant schizophrenia 3,677 European ancestry individuals, 243 Sub-Saharan African ancestry individuals, 122 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals, 244 South Asian ancestry individuals, 41 East Asian ancestry individuals, 168 NR ancestry, Other admixed ancestry individuals NA Illumina [2906712] (imputed) 3 plasma N-desmethylclozapine measurement http://www.ebi.ac.uk/efo/EFO_0600039 GCST90239837 Genome-wide genotyping array 2023-03-07 36804072 Pardinas AF 2023-03-01 Lancet Psychiatry www.ncbi.nlm.nih.gov/pubmed/36804072 Pharmacokinetics and pharmacogenomics of clozapine in an ancestrally diverse sample: a longitudinal analysis and genome-wide association study using UK clinical monitoring data. Plasma clozapine-norclozapine ratio in treatment-resistant schizophrenia 3,677 European ancestry individuals, 243 Sub-Saharan African ancestry individuals, 122 Greater Middle Eastern (Middle Eastern, North African or Persian) individuals, 244 South Asian ancestry individuals, 41 East Asian ancestry individuals, 168 NR ancestry, Other admixed ancestry individuals NA Illumina [2906712] (imputed) 3 plasma clozapine-to-N-desmethylclozapine ratio measurement http://www.ebi.ac.uk/efo/EFO_0600040 GCST90239838 Genome-wide genotyping array 2023-06-01 36769350 Khosasih V 2023-02-03 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/36769350 A Functional Polymorphism Downstream of Vitamin A Regulator Gene CYP26B1 Is Associated with Hand Osteoarthritis. Hand Osteoarthritis 420 Han Chinese ancestry cases, 716 Han Chinese ancestry controls NA Affymetrix [4587241] (imputed) 24 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90270115 Genome-wide genotyping array 2023-06-01 35670608 Edelson JL 2022-06-07 Sleep www.ncbi.nlm.nih.gov/pubmed/35670608 The Genetic Etiology of Periodic Leg Movement in Sleep. Periodic limb movement in sleep 2,747 European, African, East Asian or Native American ancestry cases, 4,096 European, African, East Asian or Native American ancestry controls NA Affymetrix, Illumina [8248889] (imputed) 2 periodic limb movement disorder http://www.ebi.ac.uk/efo/EFO_0007428 GCST90270120 Genome-wide genotyping array 2023-06-01 35670608 Edelson JL 2022-06-07 Sleep www.ncbi.nlm.nih.gov/pubmed/35670608 The Genetic Etiology of Periodic Leg Movement in Sleep. Periodic limb movement index 4,786 European ancestry individuals, 573 African ancestry individuals, 250 East Asian ancestry individuals, 491 Native American ancestry individuals NA Affymetrix, Illumina [8248889] (imputed) 2 periodic limb movement disorder http://www.ebi.ac.uk/efo/EFO_0007428 GCST90270121 Genome-wide genotyping array 2023-07-24 36890596 Yasukochi Y 2023-03-08 J Physiol Anthropol www.ncbi.nlm.nih.gov/pubmed/36890596 Cold-induced vasodilation response in a Japanese cohort: insights from cold-water immersion and genome-wide association studies. neurogenic activity response during cold exposure 94 Japanese ancestry individuals NA NR [622446] (imputed) 0 response to cold http://purl.obolibrary.org/obo/GO_0009409 GCST90271760 Genome-wide genotyping array 2023-07-24 36890596 Yasukochi Y 2023-03-08 J Physiol Anthropol www.ncbi.nlm.nih.gov/pubmed/36890596 Cold-induced vasodilation response in a Japanese cohort: insights from cold-water immersion and genome-wide association studies. eNO-independent activity response during cold exposure 94 Japanese ancestry individuals NA NR [622446] (imputed) 33 response to cold http://purl.obolibrary.org/obo/GO_0009409 GCST90271759 Genome-wide genotyping array 2023-07-24 36890596 Yasukochi Y 2023-03-08 J Physiol Anthropol www.ncbi.nlm.nih.gov/pubmed/36890596 Cold-induced vasodilation response in a Japanese cohort: insights from cold-water immersion and genome-wide association studies. Cold induced vasodilation 84 Japanese ancestry cases, 10 Japanese ancestry controls NA NR [622446] (imputed) 48 cold-induced vasodilation http://www.ebi.ac.uk/efo/EFO_0803534 GCST90271758 Genome-wide genotyping array 2023-06-15 36623684 Durand A 2022-12-26 Am J Kidney Dis www.ncbi.nlm.nih.gov/pubmed/36623684 Identification of Novel Genetic Risk Factors for Focal Segmental Glomerulosclerosis in Children: Results From the Chronic Kidney Disease in Children (CKiD) Cohort. Primary focal segmental glomerulosclerosis in chronic kidney disease 31 African American child cases, 107 African American child controls NA Illumina [680138] (imputed) 14 focal segmental glomerulosclerosis http://www.ebi.ac.uk/efo/EFO_0004236 GCST90134617 Genome-wide genotyping array 2023-04-26 36638096 Dapas M 2023-01-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36638096 Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings. Childhood lung function (FEV1/FVC z score) in low-income urban environment 886 non-Hispanic Black, Hispanic, European, Native American or East Asian ancestry children NA Illumina [14100000] 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90267983 Genome-wide sequencing 2023-04-26 36638096 Dapas M 2023-01-13 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36638096 Multi-omic association study identifies DNA methylation-mediated genotype and smoking exposure effects on lung function in children living in urban settings. Childhood lung function (FEV1 percent predicted) in low-income urban environment 606 non-Hispanic Black children, 224 Hispanic children, 57 Native American or East Asian ancestry children, 9 European ancestry children NA Illumina [14100000] 1 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90267982 Genome-wide sequencing 2023-03-22 35953101 Lee S 2022-08-11 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/35953101 Zinc finger protein 33B demonstrates sex-interaction with atopy-related markers in childhood asthma. Atopy in childhood asthma x sex interaction 28 African ancestry trios, 216 European ancestry trios, 907 Hispanic trios, 22 trios NA Illumina 2 sex interaction measurement, atopy http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0002686 GCST90258649 Genome-wide sequencing [Illumina] 2023-03-22 35953101 Lee S 2022-08-11 Eur Respir J www.ncbi.nlm.nih.gov/pubmed/35953101 Zinc finger protein 33B demonstrates sex-interaction with atopy-related markers in childhood asthma. Atopy in childhood asthma 28 African ancestry trios, 216 European ancestry trios, 907 Hispanic trios, 22 trios NA Illumina 0 atopy http://www.ebi.ac.uk/efo/EFO_0002686 GCST90258648 Genome-wide sequencing [Illumina] 2023-07-26 36632775 Zhou JY 2023-01-12 J Hum Nutr Diet www.ncbi.nlm.nih.gov/pubmed/36632775 Interaction of environmental factors with the polygenic risk scores of thinness-related genes in preventing obesity risk in middle-aged adults: The KoGES. Underweight 991 Korean ancestry middle-aged cases, 21,921 Korean ancestry middle-aged controls NA Affymetrix [NR] (imputed) 6 underweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005936 GCST90274863 Genome-wide genotyping array 2023-04-19 36385154 Klimentidis YC 2022-11-16 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36385154 Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factors. Lipedema 24,450 European ancestry female cases, 165,227 European ancestry female controls 130 cases, 5,848 female controls Affymetrix [16800000] (imputed) 0 Lipedema http://purl.obolibrary.org/obo/MONDO_0013577 GCST90267563 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. High density lipoprotein cholesterol levels 1,238,180 European, East Asian, Hispanic, admixed African or South Asian ancestry individuals 1,236 Arab ancestry individuals, 4,362 Asian ancestry individuals, 8,205 Hispanic individuals, 10,657 African ancestry individuals, 22,967 African American individuals, 28,290 South Asian ancestry individuals, 71,410 European ancestry individuals, 160,212 East Asian ancestry individuals NR [3100000] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90255502 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. High density lipoprotein cholesterol levels 562,410 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 5,806 African ancestry women, 6,075 European ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women NR [3100000] (imputed) 4 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90255503 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. High density lipoprotein cholesterol levels 749,391 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 4,851 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men NR [3100000] (imputed) 15 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90255504 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Low density lipoprotein cholesterol levels 1,238,180 European, East Asian, Hispanic, admixed African or South Asian ancestry individuals 1,236 Arab ancestry individuals, 4,362 Asian ancestry individuals, 8,205 Hispanic individuals, 10,657 African ancestry individuals, 22,967 African American individuals, 28,290 South Asian ancestry individuals, 71,410 European ancestry individuals, 160,212 East Asian ancestry individuals NR [3100000] (imputed) 1 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90255505 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Low density lipoprotein cholesterol levels 562,410 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 5,806 African ancestry women, 6,075 European ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women NR [3100000] (imputed) 3 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90255506 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Low density lipoprotein cholesterol levels 749,391 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 4,851 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men NR [3100000] (imputed) 5 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90255507 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Total cholesterol levels 1,238,180 European, East Asian, Hispanic, admixed African or South Asian ancestry individuals 1,236 Arab ancestry individuals, 4,362 Asian ancestry individuals, 8,205 Hispanic individuals, 10,657 African ancestry individuals, 22,967 African American individuals, 28,290 South Asian ancestry individuals, 71,410 European ancestry individuals, 160,212 East Asian ancestry individuals NR [3100000] (imputed) 1 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90255508 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Total cholesterol levels 562,410 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 5,806 African ancestry women, 6,075 European ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women NR [3100000] (imputed) 3 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90255509 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Total cholesterol levels 749,391 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 4,851 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men NR [3100000] (imputed) 5 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90255510 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Triglyceride levels 1,238,180 European, East Asian, Hispanic, admixed African or South Asian ancestry individuals 1,236 Arab ancestry individuals, 4,362 Asian ancestry individuals, 8,205 Hispanic individuals, 10,657 African ancestry individuals, 22,967 African American individuals, 28,290 South Asian ancestry individuals, 71,410 European ancestry individuals, 160,212 East Asian ancestry individuals NR [3100000] (imputed) 4 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90255511 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Triglyceride levels 562,410 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 5,806 African ancestry women, 6,075 European ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women NR [3100000] (imputed) 3 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90255512 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Triglyceride levels 749,391 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 4,851 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men NR [3100000] (imputed) 8 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90255513 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Non-HDL cholesterol levels 1,238,180 European, East Asian, Hispanic, admixed African or South Asian ancestry individuals 1,236 Arab ancestry individuals, 4,362 Asian ancestry individuals, 8,205 Hispanic individuals, 10,657 African ancestry individuals, 22,967 African American individuals, 28,290 South Asian ancestry individuals, 71,410 European ancestry individuals, 160,212 East Asian ancestry individuals NR [3100000] (imputed) 1 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90255514 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Non-HDL cholesterol levels 562,410 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 5,806 African ancestry women, 6,075 European ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women NR [3100000] (imputed) 4 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90255515 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Non-HDL cholesterol levels 749,391 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 4,851 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men NR [3100000] (imputed) 4 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90255516 Targeted genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. High density lipoprotein cholesterol levels up to 766,048 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 6,075 European ancestry women, 8,355 African ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women Affymetrix, Illumina [91000000] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90255517 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. High density lipoprotein cholesterol levels up to 943,600 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 6,601 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men Affymetrix, Illumina [91000000] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90255518 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Low density lipoprotein cholesterol levels up to 766,048 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 6,075 European ancestry women, 8,355 African ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women Affymetrix, Illumina [91000000] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90255519 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Low density lipoprotein cholesterol levels up to 943,600 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 6,601 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men Affymetrix, Illumina [91000000] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90255520 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Total cholesterol levels up to 766,048 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 6,075 European ancestry women, 8,355 African ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women Affymetrix, Illumina [91000000] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90255521 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Total cholesterol levels up to 943,600 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 6,601 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men Affymetrix, Illumina [91000000] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90255522 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Triglyceride levels up to 766,048 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 6,075 European ancestry women, 8,355 African ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women Affymetrix, Illumina [91000000] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90255523 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Triglyceride levels up to 943,600 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 6,601 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men Affymetrix, Illumina [91000000] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90255524 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Non-HDL cholesterol levels up to 766,048 European, East Asian, Hispanic, admixed African or South Asian ancestry women 305 Asian ancestry women, 609 Arab ancestry women, 902 Hispanic women, 5,455 African American women, 6,075 European ancestry women, 8,355 African ancestry women, 13,154 South Asian ancestry women, 103,198 East Asian ancestry women Affymetrix, Illumina [91000000] (imputed) 0 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90255525 Genome-wide genotyping array 2023-03-08 36575460 Kanoni S 2022-12-27 Genome Biol www.ncbi.nlm.nih.gov/pubmed/36575460 Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Non-HDL cholesterol levels up to 943,600 European, East Asian, Hispanic, admixed African or South Asian ancestry men 626 Arab ancestry men, 4,056 Asian ancestry men, 6,601 African ancestry men, 7,302 Hispanic men, 15,135 South Asian ancestry men, 17,511 African American men, 57,013 East Asian ancestry men, 65,334 European ancestry men Affymetrix, Illumina [91000000] (imputed) 0 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90255526 Genome-wide genotyping array 2023-07-24 37033211 Mansour A 2023-03-23 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37033211 Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses. Diabetic retinopathy in type 2 diabetes 62 Emirati ancestry cases, 248 Emirati ancestry controls NA Illumina [39840] 0 diabetic retinopathy http://www.ebi.ac.uk/efo/EFO_0003770 GCST90274754 Targeted genotyping array [Exome-24 array] 2023-07-24 37033211 Mansour A 2023-03-23 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37033211 Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses. Diabetic neuropathy in type 2 diabetes 47 Emirati ancestry cases, 263 Emirati ancestry controls NA Illumina [39840] 0 diabetic neuropathy http://www.ebi.ac.uk/efo/EFO_1000783 GCST90274755 Targeted genotyping array [Exome-24 array] 2023-07-24 37033211 Mansour A 2023-03-23 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37033211 Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses. Diabetic nephropathy in type 2 diabetes 22 Emirati ancestry cases, 288 Emirati ancestry controls NA Illumina [39840] 0 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90274756 Targeted genotyping array [Exome-24 array] 2023-07-24 37033211 Mansour A 2023-03-23 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37033211 Microvascular and macrovascular complications of type 2 diabetes mellitus: Exome wide association analyses. Cardiovascular disease in type 2 diabetes 42 Emirati ancestry cases, 268 Emirati ancestry controls NA Illumina [39840] 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90274757 Targeted genotyping array [Exome-24 array] 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Tuberculosis 1,532 Chinese Han ancestry cases, 1,584 Chinese Han ancestry controls NA Illumina [4096530] (imputed) 20 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90275067 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Tuberculosis 612 Chinese Han ancestry female cases, 741 Chinese Han ancestry female controls NA Illumina [NR] (imputed) 5 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90275068 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Tuberculosis 920 Chinese Han ancestry male cases, 843 Chinese Han ancestry male controls NA Illumina [NR] (imputed) 4 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90275069 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Tuberculosis up to 1,532 Chinese Han ancestry cases aged <45 years, up to 1,584 Chinese Han ancestry controls aged <45 years NA Illumina [NR] (imputed) 11 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90275070 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Tuberculosis up to 1,532 Chinese Han ancestry cases aged >=45 years, up to 1,584 Chinese Han ancestry controls aged >=45 years NA Illumina [NR] (imputed) 5 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90275071 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Extrapulmonary tuberculosis 330 Chinese Han ancestry cases, 1,584 Chinese Han ancestry controls NA Illumina [NR] (imputed) 9 extrapulmonary tuberculosis http://purl.obolibrary.org/obo/MONDO_0000368 GCST90275072 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Pulmonary tuberculosis 1,202 Chinese Han ancestry cases, 1,584 Chinese Han ancestry controls NA Illumina [NR] (imputed) 10 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90275073 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Tuberculosis 211 Chinese Tibetan ancestry cases, 228 Chinese Tibetan ancestry controls NA Illumina [3826379] (imputed) 8 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90275074 Genome-wide genotyping array 2023-08-02 37009413 Bai H 2023-03-29 MedComm (2020) www.ncbi.nlm.nih.gov/pubmed/37009413 Genome-wide association study of tuberculosis in the western Chinese Han and Tibetan population. Tuberculosis 1,743 Chinese Tibetan, Chinese Han ancestry cases, 1,812 Chinese Tibetan, Chinese Han ancestry controls 1,382 Chinese Han, Japanese ancestry cases, 213,124 Chinese Han, Japanese ancestry controls Illumina [3826379] (imputed) 1 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90275075 Genome-wide genotyping array 2023-04-03 36508697 Wang X 2022-12-12 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/36508697 Genome-Wide Association Study Identifies ROBO2 as a Novel Susceptibility Gene for Anthracycline-Related Cardiomyopathy in Childhood Cancer Survivors. Cardiomyopathy in anthracycline-exposed childhood cancer survivors x anthracycline dose interaction 126 European ancestry cases, 1,740 European ancestry controls 79 European ancestry cases, 140 European ancestry controls, 12 Hispanic cases, 5 Hispanic controls, 9 African American cases, 9 African American controls, 5 cases, 6 controls Illumina [6131740] (imputed) 0 response to anthracycline-based chemotherapy, cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0005257, http://www.ebi.ac.uk/efo/EFO_0000318 GCST90267155 Genome-wide genotyping array 2023-04-03 36508697 Wang X 2022-12-12 J Clin Oncol www.ncbi.nlm.nih.gov/pubmed/36508697 Genome-Wide Association Study Identifies ROBO2 as a Novel Susceptibility Gene for Anthracycline-Related Cardiomyopathy in Childhood Cancer Survivors. Cardiomyopathy in anthracycline-exposed childhood cancer survivors 126 European ancestry cases, 1,740 European ancestry controls NA Illumina [6131740] (imputed) 1 response to anthracycline-based chemotherapy, cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0005257, http://www.ebi.ac.uk/efo/EFO_0000318 GCST90267154 Genome-wide genotyping array 2023-06-21 36737699 Muckian MD 2023-02-03 BMC Infect Dis www.ncbi.nlm.nih.gov/pubmed/36737699 Mendelian randomisation identifies priority groups for prophylactic EBV vaccination. Epstein-Barr virus seropositivity 7,795 European ancestry cases, 449 European ancestry controls NA Affymetrix [NR] (imputed) 2 Epstein-Barr virus seropositivity http://www.ebi.ac.uk/efo/EFO_0010908 GCST90270367 Genome-wide genotyping array 2023-07-26 37107557 Kyrgiafini MA 2023-03-26 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/37107557 Gene-by-Sex Interactions: Genome-Wide Association Study Reveals Five SNPs Associated with Obesity and Overweight in a Male Population. Overweight 118 European ancestry male cases, 94 European ancestry male controls NA Illumina [362108] (imputed) 4 overweight body mass index status http://www.ebi.ac.uk/efo/EFO_0005935 GCST90274857 Genome-wide genotyping array 2023-07-26 37107557 Kyrgiafini MA 2023-03-26 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/37107557 Gene-by-Sex Interactions: Genome-Wide Association Study Reveals Five SNPs Associated with Obesity and Overweight in a Male Population. Obesity 57 European ancestry male cases, 94 European ancestry male controls NA Illumina [356016] (imputed) 1 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90274858 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular end diastolic volume (adjusted without BSA and SBP) 35,941 European ancestry individuals NA Affymetrix [9423903] (imputed) 0 right ventricular diastolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021814 GCST90268141 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular ejection fraction (adjusted without BSA and SBP) 35,875 European ancestry individuals NA Affymetrix [9248475] (imputed) 0 right ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0021816 GCST90268142 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular end systolic volume (adjusted without BSA and SBP) 35,928 European ancestry individuals NA Affymetrix [8658655] (imputed) 0 right ventricular systolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021815 GCST90268143 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular peak atrial filling rate (adjusted without BSA and SBP) 35,899 European ancestry individuals NA Affymetrix [10152925] (imputed) 0 right ventricular function http://www.ebi.ac.uk/efo/EFO_0020939 GCST90268144 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular peak ejection rate (adjusted without BSA and SBP) 35,928 European ancestry individuals NA Affymetrix [10152917] (imputed) 0 right ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0021816 GCST90268145 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular peak filling rate (adjusted without BSA and SBP) 35,883 European ancestry individuals NA Affymetrix [10152659] (imputed) 0 right ventricular function http://www.ebi.ac.uk/efo/EFO_0020939 GCST90268146 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular stroke volume (adjusted without BSA and SBP) 35,932 European ancestry individuals NA Affymetrix [10152902] (imputed) 0 right ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0021817 GCST90268147 Genome-wide genotyping array 2023-05-04 37069358 Cosentino J 2023-04-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37069358 Inference of chronic obstructive pulmonary disease with deep learning on raw spirograms identifies new genetic loci and improves risk models. Chronic obstructive pulmonary disease liability (machine learning-based score) 325,027 European ancestry individuals NA Affymetrix [13285083] (imputed) 356 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90244098 Genome-wide genotyping array 2023-05-22 37120605 Barry A 2023-04-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37120605 Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Pediatric steroid sensitive nephrotic syndrome 674 European ancestry cases, 6,817 European ancestry controls, 109 African ancestry cases, 7,514 African ancestry controls, 1,311 East Asian ancestry cases, 7,780 East Asian ancestry controls, 193 South Asian ancestry cases, 436 South Asian ancestry controls, 55 Maghrebian ancestry cases, 228 Maghrebian ancestry controls, 98 Other admixed ancestry ancestry cases, 13,248 Other admixed ancestry ancestry controls NA Affymetrix, Illumina [18066346] (imputed) 27 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90258619 Genome-wide genotyping array 2023-05-22 37120605 Barry A 2023-04-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37120605 Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Pediatric steroid sensitive nephrotic syndrome 109 African ancestry cases, 7,514 African ancestry controls NA Illumina [14302064] (imputed) 1 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90269966 Genome-wide genotyping array 2023-05-22 37120605 Barry A 2023-04-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37120605 Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Pediatric steroid sensitive nephrotic syndrome 1,311 East Asian ancestry cases, 7,780 East Asian ancestry controls NA Affymetrix, Illumina [8644038] (imputed) 7 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90269967 Genome-wide genotyping array 2023-05-22 37120605 Barry A 2023-04-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37120605 Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Pediatric steroid sensitive nephrotic syndrome 1,096 European ancestry cases, 12,459 European ancestry controls NA Illumina [8414111] (imputed) 7 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90269968 Genome-wide genotyping array 2023-05-22 37120605 Barry A 2023-04-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37120605 Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome. Pediatric steroid sensitive nephrotic syndrome 193 South Asian ancestry cases, 436 South Asian ancestry controls NA Illumina [8460574] (imputed) 1 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90269969 Genome-wide genotyping array 2023-02-23 36515925 Kimbrel NA 2022-12-14 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36515925 Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans. Suicidal thoughts and behaviors 75,941 European ancestry cases, 376,826 European ancestry controls, 30,283 African ancestry cases, 90,835 African ancestry controls, 13,230 Hispanic cases, 38,378 Hispanic controls, 1,757 Asian ancestry cases, 6,528 Asian ancestry controls NA NR [NR] (imputed) 7 suicidal ideation, suicide behaviour http://www.ebi.ac.uk/efo/EFO_0004320, http://www.ebi.ac.uk/efo/EFO_0007623 GCST90246333 Genome-wide genotyping array 2023-02-23 36515925 Kimbrel NA 2022-12-14 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36515925 Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans. Suicidal thoughts and behaviors 75,941 European ancestry cases, 376,826 European ancestry controls NA NR [NR] (imputed) 12 suicidal ideation, suicide behaviour http://www.ebi.ac.uk/efo/EFO_0004320, http://www.ebi.ac.uk/efo/EFO_0007623 GCST90246334 Genome-wide genotyping array 2023-02-23 36515925 Kimbrel NA 2022-12-14 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36515925 Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans. Suicidal thoughts and behaviors 30,283 African ancestry cases, 90,835 African ancestry controls NA NR [NR] (imputed) 1 suicidal ideation, suicide behaviour http://www.ebi.ac.uk/efo/EFO_0004320, http://www.ebi.ac.uk/efo/EFO_0007623 GCST90246335 Genome-wide genotyping array 2023-02-23 36515925 Kimbrel NA 2022-12-14 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36515925 Identification of Novel, Replicable Genetic Risk Loci for Suicidal Thoughts and Behaviors Among US Military Veterans. Suicidal thoughts and behaviors 13,230 Hispanic cases, 38,378 Hispanic controls NA NR [NR] (imputed) 1 suicidal ideation, suicide behaviour http://www.ebi.ac.uk/efo/EFO_0004320, http://www.ebi.ac.uk/efo/EFO_0007623 GCST90246336 Genome-wide genotyping array 2023-03-21 36672180 Tirozzi A 2023-01-06 Cells www.ncbi.nlm.nih.gov/pubmed/36672180 A Multi-Trait Association Analysis of Brain Disorders and Platelet Traits Identifies Novel Susceptibility Loci for Major Depression, Alzheimer's and Parkinson's Disease. Major depressive disorder (MTAG) at least 246,363 European ancestry cases, at least 561,190 European ancestry controls NA NR [4540326] 2 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90256605 Genome-wide genotyping array 2023-03-21 36672180 Tirozzi A 2023-01-06 Cells www.ncbi.nlm.nih.gov/pubmed/36672180 A Multi-Trait Association Analysis of Brain Disorders and Platelet Traits Identifies Novel Susceptibility Loci for Major Depression, Alzheimer's and Parkinson's Disease. Mean platelet volume (MTAG) at least 408,112 European ancestry individuals NA NR [4540326] 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90256606 Genome-wide genotyping array 2023-03-21 36672180 Tirozzi A 2023-01-06 Cells www.ncbi.nlm.nih.gov/pubmed/36672180 A Multi-Trait Association Analysis of Brain Disorders and Platelet Traits Identifies Novel Susceptibility Loci for Major Depression, Alzheimer's and Parkinson's Disease. Platelet distribution width (MTAG) at least 408,112 European ancestry individuals NA NR [4540326] 0 platelet component distribution width http://www.ebi.ac.uk/efo/EFO_0007984 GCST90256607 Genome-wide genotyping array 2023-03-21 36672180 Tirozzi A 2023-01-06 Cells www.ncbi.nlm.nih.gov/pubmed/36672180 A Multi-Trait Association Analysis of Brain Disorders and Platelet Traits Identifies Novel Susceptibility Loci for Major Depression, Alzheimer's and Parkinson's Disease. Platelet count (MTAG) at least 408,112 European ancestry individuals NA NR [4540326] 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90256608 Genome-wide genotyping array 2023-11-22 37247657 Hollis B 2023-05-27 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/37247657 Lifetime risk and genetic predisposition to post-traumatic OA of the knee in the UK Biobank. Post-traumatic osteoarthritis of knee (time to event) 377 European ancestry post-injury cases, 2,697 European ancestry post-injury controls NA NR [NR] (imputed) 1 age at diagnosis, osteoarthritis, knee, knee injury http://www.ebi.ac.uk/efo/EFO_0004918, http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0009507 GCST90297777 Genome-wide genotyping array 2023-11-22 37247657 Hollis B 2023-05-27 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/37247657 Lifetime risk and genetic predisposition to post-traumatic OA of the knee in the UK Biobank. Knee injury 3,074 European ancestry cases, 30,226 European ancestry controls NA NR [NR] (imputed) 4 knee injury http://www.ebi.ac.uk/efo/EFO_0009507 GCST90297778 Genome-wide genotyping array 2023-11-22 37247657 Hollis B 2023-05-27 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/37247657 Lifetime risk and genetic predisposition to post-traumatic OA of the knee in the UK Biobank. Idiopathic knee osteoarthritis 90,888 European ancestry cases, 263,673 European ancestry controls NA NR [NR] (imputed) 64 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90297779 Genome-wide genotyping array 2023-05-24 36769103 Bau DT 2023-02-01 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/36769103 A Genome-Wide Association Study Identified Novel Genetic Susceptibility Loci for Oral Cancer in Taiwan. Oral cancer 1,529 Taiwanese ancestry cases, 44,572 Taiwanese ancestry controls NA Affymetrix [15277414] (imputed) 3 mouth neoplasm http://www.ebi.ac.uk/efo/EFO_0003868 GCST90269972 Genome-wide genotyping array 2023-03-10 36872133 Chen F 2023-02-27 Eur Urol www.ncbi.nlm.nih.gov/pubmed/36872133 Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry. Prostate cancer 19,378 African ancestry men cases, 61,620 African ancestry men controls NA Affymetrix, Illumina [27753840] (imputed) 9 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90255678 Genome-wide genotyping array 2023-03-08 36804406 Al-Janabi A 2023-02-15 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/36804406 Atopic polygenic risk score is associated with paradoxical eczema developing in psoriasis patients treated with biologics. Paradoxical eczema in biologic-treated plaque psoriasis 88 European ancestry cases, 3,124 European ancestry controls NA Illumina [7414955] (imputed) 2 atopic eczema, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0000274, http://purl.obolibrary.org/obo/GO_0009410 GCST90162550 Exome genotyping array [HumanOmniExpressExome-8 v1.2, 1.3 and 1.6] 2023-03-31 36437532 Grgic O 2022-11-27 J Dent Res www.ncbi.nlm.nih.gov/pubmed/36437532 Novel Genetic Determinants of Dental Maturation in Children. Dental development 14,805 European or unknown ancestry individuals NA Illumina [2216657] (imputed) 13 number of teeth measurement http://www.ebi.ac.uk/efo/EFO_0010073 GCST90266934 Genome-wide genotyping array 2023-06-14 36606461 Ke J 2023-01-06 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/36606461 Exploring the Genetic Association between Obesity and Serum Lipid Levels Using Bivariate Methods. Body mass index and total cholesterol levels 457 Chinese ancestry individuals from twin pairs 289 Chinese ancestry individuals from twin pairs Illumina [5144874] (imputed) 0 total cholesterol measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90270288 Genome-wide genotyping array 2023-06-14 36606461 Ke J 2023-01-06 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/36606461 Exploring the Genetic Association between Obesity and Serum Lipid Levels Using Bivariate Methods. Body mass index and triglyceride levels 457 Chinese ancestry individuals from twin pairs 289 Chinese ancestry individuals from twin pairs Illumina [5144874] (imputed) 0 triglyceride measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90270289 Genome-wide genotyping array 2023-06-14 36606461 Ke J 2023-01-06 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/36606461 Exploring the Genetic Association between Obesity and Serum Lipid Levels Using Bivariate Methods. Body mass index and high density lipoprotein cholesterol levels 457 Chinese ancestry individuals from twin pairs 289 Chinese ancestry individuals from twin pairs Illumina [5144874] (imputed) 0 body mass index, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004340, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90270290 Genome-wide genotyping array 2023-06-14 36606461 Ke J 2023-01-06 Twin Res Hum Genet www.ncbi.nlm.nih.gov/pubmed/36606461 Exploring the Genetic Association between Obesity and Serum Lipid Levels Using Bivariate Methods. Body mass index and low density lipoprotein cholesterol levels 457 Chinese ancestry individuals from twin pairs 289 Chinese ancestry individuals from twin pairs Illumina [5144874] (imputed) 0 low density lipoprotein cholesterol measurement, body mass index http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90270291 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Red vs non-red hair color 34 Iberian ancestry cases, 4,945 Iberian ancestry controls NA Illumina [10216971] (imputed) 54 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST90255681 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Blond vs. brown/black hair color 243 Iberian ancestry cases, 4,702 Iberian ancestry controls NA Illumina [10216971] (imputed) 17 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST90255682 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Brown vs. black hair color 3,750 Iberian ancestry cases, 952 Iberian ancestry controls NA Illumina [10216971] (imputed) 22 hair color http://www.ebi.ac.uk/efo/EFO_0003924 GCST90255683 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Eye color 4,987 Iberian ancestry individuals NA Illumina [10216971] (imputed) 97 eye color http://www.ebi.ac.uk/efo/EFO_0003949 GCST90255684 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Freckles 4,984 Iberian ancestry individuals NA Illumina [10216971] (imputed) 7 freckles http://www.ebi.ac.uk/efo/EFO_0003963 GCST90255685 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Ease of sunburn 4,985 Iberian ancestry individuals NA Illumina [10216971] (imputed) 28 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90255686 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Ease of skin tanning 4,973 Iberian ancestry individuals NA Illumina [10216971] (imputed) 25 skin sensitivity to sun http://www.ebi.ac.uk/efo/EFO_0004795 GCST90255687 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Skin phototype score 4,933 Iberian ancestry individuals NA Illumina [10216971] (imputed) 111 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90255688 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Skin color (Fitzpatrick scale) 4,933 Iberian ancestry individuals NA Illumina [10216971] (imputed) 82 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90255689 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Skin color 4,985 Iberian ancestry individuals NA Illumina [10216971] (imputed) 66 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90255690 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Sunscreen use outside 4,918 Iberian ancestry individuals NA Illumina [10216971] (imputed) 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90255691 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Sunscreen use when suntanning 4,352 Iberian ancestry individuals NA Illumina [10216971] (imputed) 0 sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0010729 GCST90255692 Genome-wide genotyping array 2023-03-10 36672889 Farre X 2023-01-05 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672889 Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort. Weekly hours spent outside 4,797 Iberian ancestry individuals NA Illumina [10216971] (imputed) 0 time spent outdoors measurement http://www.ebi.ac.uk/efo/EFO_0600081 GCST90255693 Genome-wide genotyping array 2023-03-21 36314488 Durda P 2022-10-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36314488 Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study. Soluble CD163 levels 2,838 European ancestry individuals 939 European ancestry individuals NR [306665] (imputed) 2 soluble CD163 measurement http://www.ebi.ac.uk/efo/EFO_0020072 GCST90244700 Genome-wide genotyping array 2023-03-21 36314488 Durda P 2022-10-31 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/36314488 Circulating Soluble CD163, Associations With Cardiovascular Outcomes and Mortality, and Identification of Genetic Variants in Older Individuals: The Cardiovascular Health Study. Soluble CD163 levels 763 African American individuals NA NR [306665] (imputed) 2 soluble CD163 measurement http://www.ebi.ac.uk/efo/EFO_0020072 GCST90244701 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular end diastolic volume 35,941 European ancestry individuals NA Affymetrix [10129571] (imputed) 11 right ventricular diastolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021814 GCST90268116 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular ejection fraction 35,875 European ancestry individuals NA Affymetrix [10129492] (imputed) 12 right ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0021816 GCST90268117 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular end systolic volume 35,928 European ancestry individuals NA Affymetrix [10129455] (imputed) 20 right ventricular systolic volume measurement http://www.ebi.ac.uk/efo/EFO_0021815 GCST90268118 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular peak atrial filling rate 35,899 European ancestry individuals NA Affymetrix [10129585] (imputed) 1 right ventricular function http://www.ebi.ac.uk/efo/EFO_0020939 GCST90268119 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular peak ejection rate 35,928 European ancestry individuals NA Affymetrix [10129580] (imputed) 2 right ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0021816 GCST90268120 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular peak filling rate 35,883 European ancestry individuals NA Affymetrix [10129320] (imputed) 0 right ventricular function http://www.ebi.ac.uk/efo/EFO_0020939 GCST90268121 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Right ventricular stroke volume 35,932 European ancestry individuals NA Affymetrix [10129563] (imputed) 5 right ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0021817 GCST90268122 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end diastolic mass 32,530 European ancestry individuals NA Affymetrix [10128045] (imputed) 6 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST90268123 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end-diastolic volume 32,525 European ancestry individuals NA Affymetrix [10128036] (imputed) 6 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST90268124 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular ejection fraction 32,532 European ancestry individuals NA Affymetrix [10128034] (imputed) 15 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST90268125 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end-systolic volume 32,528 European ancestry individuals NA Affymetrix [10128021] (imputed) 14 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST90268126 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular peak atrial filling rate 32,531 European ancestry individuals NA Affymetrix [10128000] (imputed) 0 left ventricular function http://www.ebi.ac.uk/efo/EFO_0004295 GCST90268127 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular peak ejection rate 32,532 European ancestry individuals NA Affymetrix [10128036] (imputed) 0 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST90268128 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular peak filling rate 32,526 European ancestry individuals NA Affymetrix [10127975] (imputed) 0 left ventricular function http://www.ebi.ac.uk/efo/EFO_0004295 GCST90268129 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular stroke volume 32,528 European ancestry individuals NA Affymetrix [10128034] (imputed) 4 left ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0010555 GCST90268130 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end diastolic mass end diastolic volume ratio 32,520 European ancestry individuals NA Affymetrix [10128045] (imputed) 14 Left ventricular mass to end-diastolic volume ratio http://www.ebi.ac.uk/efo/EFO_0010556 GCST90268131 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end diastolic mass (adjusted without BSA and SBP) 32,530 European ancestry individuals NA Affymetrix [10128036] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST90268132 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end-diastolic volume (adjusted without BSA and SBP) 32,525 European ancestry individuals NA Affymetrix [10128036] (imputed) 0 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST90268133 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular ejection fraction (adjusted without BSA and SBP) 32,532 European ancestry individuals NA Affymetrix [10128034] (imputed) 0 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST90268134 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end-systolic volume (adjusted without BSA and SBP) 32,528 European ancestry individuals NA Affymetrix [10128021] (imputed) 0 left ventricular systolic function measurement http://www.ebi.ac.uk/efo/EFO_0008206 GCST90268135 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular peak atrial filling rate (adjusted without BSA and SBP) 32,531 European ancestry individuals NA Affymetrix [10128000] (imputed) 0 left ventricular function http://www.ebi.ac.uk/efo/EFO_0004295 GCST90268136 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular peak ejection rate (adjusted without BSA and SBP) 32,532 European ancestry individuals NA Affymetrix [10128036] (imputed) 0 left ventricular ejection fraction measurement http://www.ebi.ac.uk/efo/EFO_0008373 GCST90268137 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular peak filling rate (adjusted without BSA and SBP) 32,526 European ancestry individuals NA Affymetrix [10127975] (imputed) 0 left ventricular function http://www.ebi.ac.uk/efo/EFO_0004295 GCST90268138 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular stroke volume (adjusted without BSA and SBP) 32,528 European ancestry individuals NA Affymetrix [10128034] (imputed) 0 left ventricular stroke volume measurement http://www.ebi.ac.uk/efo/EFO_0010555 GCST90268139 Genome-wide genotyping array 2023-06-07 37126556 Schmidt AF 2023-04-26 Sci Adv www.ncbi.nlm.nih.gov/pubmed/37126556 Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity. Left ventricular end diastolic mass end diastolic volume ratio (adjusted without BSA and SBP) 32,520 European ancestry individuals NA Affymetrix [10128045] (imputed) 0 Left ventricular mass to end-diastolic volume ratio http://www.ebi.ac.uk/efo/EFO_0010556 GCST90268140 Genome-wide genotyping array 2023-03-21 36662418 Faber BG 2023-01-20 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36662418 A GWAS meta-analysis of alpha angle suggests cam-type morphology may be a specific feature of hip osteoarthritis in older adults. Alpha angle 44,214 European ancestry individuals NA Affymetrix, Illumina [9134976] (imputed) 8 alpha angle measurement http://www.ebi.ac.uk/efo/EFO_0020071 GCST90129635 Genome-wide genotyping array 2023-05-23 37156767 Sethi A 2023-05-08 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37156767 Genetics implicates overactive osteogenesis in the development of diffuse idiopathic skeletal hyperostosis. Diffuse idiopathic skeletal hyperostosis flow score 33,413 European ancestry individuals NA Affymetrix [9911384] (imputed) 12 diffuse idiopathic skeletal hyperostosis http://www.ebi.ac.uk/efo/EFO_0007236 GCST90134532 Genome-wide genotyping array 2023-06-27 36802703 Small AM 2023-02-20 Circulation www.ncbi.nlm.nih.gov/pubmed/36802703 Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Calcific aortic valve stenosis 12,395 European ancestry cases, 287,787 European ancestry controls 11,433 European ancestry cases, 254,839 European ancestry controls Affymetrix [NR] (imputed) 5 aortic stenosis, aortic valve calcification http://www.ebi.ac.uk/efo/EFO_0000266, http://www.ebi.ac.uk/efo/EFO_0005239 GCST90271563 Genome-wide genotyping array 2023-06-27 36802703 Small AM 2023-02-20 Circulation www.ncbi.nlm.nih.gov/pubmed/36802703 Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Calcific aortic valve stenosis 1,445 black cases, 79,299 black controls 1,110 black cases, 64,397 black controls Affymetrix [NR] (imputed) 0 aortic stenosis, aortic valve calcification http://www.ebi.ac.uk/efo/EFO_0000266, http://www.ebi.ac.uk/efo/EFO_0005239 GCST90271564 Genome-wide genotyping array 2023-06-27 36802703 Small AM 2023-02-20 Circulation www.ncbi.nlm.nih.gov/pubmed/36802703 Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Calcific aortic valve stenosis 611 Hispanic cases, 31,458 Hispanic controls 346 Hispanic cases, 28,858 Hispanic controls Affymetrix [NR] (imputed) 0 aortic stenosis, aortic valve calcification http://www.ebi.ac.uk/efo/EFO_0000266, http://www.ebi.ac.uk/efo/EFO_0005239 GCST90271565 Genome-wide genotyping array 2023-06-27 36802703 Small AM 2023-02-20 Circulation www.ncbi.nlm.nih.gov/pubmed/36802703 Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program. Calcific aortic valve stenosis 12,395 European ancestry cases, 287,787 European ancestry controls, 1,445 black cases, 79,299 black controls, 611 Hispanic cases, 31,458 Hispanic controls 11,433 European ancestry cases, 254,839 European ancestry controls, 1,110 black cases, 64,397 black controls, 346 Hispanic cases, 28,858 Hispanic controls Affymetrix [14304921] (imputed) 5 aortic stenosis, aortic valve calcification http://www.ebi.ac.uk/efo/EFO_0000266, http://www.ebi.ac.uk/efo/EFO_0005239 GCST90271566 Genome-wide genotyping array 2023-06-28 37325711 Lu Q 2022-12-05 Phenomics www.ncbi.nlm.nih.gov/pubmed/37325711 A Genome-Wide Association Study for Susceptibility to Axial Length in Highly Myopic Eyes. Axial length in high myopia 350 Chinese ancestry individuals NA NR [976429] 4 axial length measurement http://www.ebi.ac.uk/efo/EFO_0005318 GCST90271571 Genome-wide sequencing 2023-05-26 37195282 Juodakis J 2023-05-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37195282 Time-varying effects are common in genetic control of gestational duration. Gestational age at birth (maternal effect) 22,247 European ancestry individuals NA Illumina [7874836] (imputed) 2 gestational age, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90268419 Genome-wide genotyping array 2023-05-26 37195282 Juodakis J 2023-05-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37195282 Time-varying effects are common in genetic control of gestational duration. Preterm birth (maternal effect) 610 European ancestry cases, 21,637 European ancestry controls NA Illumina [7874836] (imputed) 0 premature birth, parental genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0003917, http://www.ebi.ac.uk/efo/EFO_0005939 GCST90268420 Genome-wide genotyping array 2023-05-26 37195282 Juodakis J 2023-05-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37195282 Time-varying effects are common in genetic control of gestational duration. Gestational age at birth (child effect) 21,262 European ancestry individuals NA Illumina [7876514] (imputed) 1 gestational age, fetal genotype effect measurement http://www.ebi.ac.uk/efo/EFO_0005112, http://www.ebi.ac.uk/efo/EFO_0007959 GCST90268421 Genome-wide genotyping array 2023-05-26 37195282 Juodakis J 2023-05-17 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37195282 Time-varying effects are common in genetic control of gestational duration. Preterm birth (child effect) 529 European ancestry cases, 20,733 European ancestry controls NA Illumina [7876514] (imputed) 0 fetal genotype effect measurement, premature birth http://www.ebi.ac.uk/efo/EFO_0007959, http://www.ebi.ac.uk/efo/EFO_0003917 GCST90268422 Genome-wide genotyping array 2023-05-04 35097025 de Haan A 2022-01-14 Front Cardiovasc Med www.ncbi.nlm.nih.gov/pubmed/35097025 Genetic Determinants of Serum Calcification Propensity and Cardiovascular Outcomes in the General Population. Serum calciprotein particle maturation time (T50) 2,739 European ancestry individuals NA Illumina [NR] (imputed) 3 cardiovascular disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005278 GCST90102513 Genome-wide genotyping array 2023-03-22 35964923 Timoteo VJ 2022-08-11 J Nutr Biochem www.ncbi.nlm.nih.gov/pubmed/35964923 Common and Ethnic-Specific Genetic Determinants of Hemoglobin Concentration between Taiwanese Han Chinese and European Whites: Findings from Comparative Two-Stage Genome-Wide Association Studies. Hemoglobin concentration 18,685 Han Chinese ancestry females 23,009 Han Chinese ancestry females NR [281547] 12 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90258651 Genome-wide genotyping array 2023-03-22 35964923 Timoteo VJ 2022-08-11 J Nutr Biochem www.ncbi.nlm.nih.gov/pubmed/35964923 Common and Ethnic-Specific Genetic Determinants of Hemoglobin Concentration between Taiwanese Han Chinese and European Whites: Findings from Comparative Two-Stage Genome-Wide Association Studies. Hemoglobin concentration 46,904 European ancestry males 80,822 European ancestry males NR [347791] 194 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90258652 Genome-wide genotyping array 2023-03-22 35964923 Timoteo VJ 2022-08-11 J Nutr Biochem www.ncbi.nlm.nih.gov/pubmed/35964923 Common and Ethnic-Specific Genetic Determinants of Hemoglobin Concentration between Taiwanese Han Chinese and European Whites: Findings from Comparative Two-Stage Genome-Wide Association Studies. Hemoglobin concentration 52,141 European ancestry females 89,584 European ancestry females NR [347791] 224 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90258653 Genome-wide genotyping array 2023-03-22 35964923 Timoteo VJ 2022-08-11 J Nutr Biochem www.ncbi.nlm.nih.gov/pubmed/35964923 Common and Ethnic-Specific Genetic Determinants of Hemoglobin Concentration between Taiwanese Han Chinese and European Whites: Findings from Comparative Two-Stage Genome-Wide Association Studies. Hemoglobin concentration 8,550 Han Chinese ancestry males 10,274 Han Chinese ancestry males NR [281547] 7 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90258650 Genome-wide genotyping array 2023-06-05 36343773 Chang D 2022-11-04 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/36343773 A genome wide association study of chronic spontaneous urticaria risk and heterogeneity. Chronic spontaneous urticaria 679 European ancestry, NR ancestry cases, 4,446 European ancestry, NR ancestry controls NA Illumina [10077611] (imputed) 2 urticaria http://www.ebi.ac.uk/efo/EFO_0005531 GCST90270128 Genome-wide genotyping array 2023-06-23 37248299 Honigberg MC 2023-05-29 Nat Med www.ncbi.nlm.nih.gov/pubmed/37248299 Polygenic prediction of preeclampsia and gestational hypertension. Preeclampsia or eclampsia 3,223 Asian ancestry cases, 96,119 Asian ancestry controls, 20 African ancestry cases, 1,406 African ancestry controls, 14 Hispanic or Latin American cases, 2,457 Hispanic or Latin American controls, 1,389 European ancestry cases, 351,259 European ancestry controls 410 African ancestry cases, 7,385 African ancestry controls, 48 Hispanic or Latin American cases, 615 Hispanic or Latin American controls, 2,456 European ancestry cases, 243,876 European ancestry controls Affymetrix, Illumina [NR] (imputed) 14 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90271316 Genome-wide genotyping array 2023-06-23 37248299 Honigberg MC 2023-05-29 Nat Med www.ncbi.nlm.nih.gov/pubmed/37248299 Polygenic prediction of preeclampsia and gestational hypertension. Gestational hypertension 844 Asian ancestry cases, 12,098 Asian ancestry controls, 38 African ancestry cases, 1,388 African ancestry controls, 35 Hispanic or Latin American cases, 2,436 Hispanic or Latin American controls, 8,044 European ancestry cases, 169,003 European ancestry controls 417 African ancestry cases, 7,385 African ancestry controls, 87 Hispanic or Latin American cases, 615 Hispanic or Latin American controls, 1,562 European ancestry cases, 219,863 European ancestry controls Affymetrix, Illumina [NR] (imputed) 8 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90271317 Genome-wide genotyping array 2023-06-23 37248299 Honigberg MC 2023-05-29 Nat Med www.ncbi.nlm.nih.gov/pubmed/37248299 Polygenic prediction of preeclampsia and gestational hypertension. Preeclampsia or eclampsia (MTAG) at least 3,223 Asian ancestry cases, at least 96,119 Asian ancestry controls, at least 20 African ancestry cases, at least 1,406 African ancestry controls, at least 14 Hispanic or Latin American cases, at least 2,457 Hispanic or Latin American controls, at least 1,389 European ancestry cases, at least 351,259 European ancestry controls (MTAG boosted by gestational hypertension samples) NA Affymetrix, Illumina [NR] (imputed) 2 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90271318 Genome-wide genotyping array 2023-06-27 36811322 Zhang L 2023-02-22 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/36811322 A genome-wide association study identified new variants associated with mathematical abilities in Chinese children. Mathematical reasoning 1,134 Chinese ancestry children NA Illumina [5406859] (imputed) 1 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST90271577 Genome-wide genotyping array 2023-06-27 36811322 Zhang L 2023-02-22 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/36811322 A genome-wide association study identified new variants associated with mathematical abilities in Chinese children. Spatial conception ability 1,144 Chinese ancestry children NA Illumina [5406859] (imputed) 1 mathematical ability http://www.ebi.ac.uk/efo/EFO_0004875 GCST90271578 Genome-wide genotyping array 2023-10-06 37196047 Joo YY 2023-05-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/37196047 Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. Diverticulosis 12,577 European ancestry, African ancestry, NR cases, 9,200 European ancestry, African ancestry, NR controls NA Affymetrix, Illumina [9848164] (imputed) 3 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90293093 Genome-wide genotyping array 2023-10-06 37196047 Joo YY 2023-05-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/37196047 Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. Diverticulitis 1,265 European ancestry, African ancestry, NR cases, 9,200 European ancestry, African ancestry, NR controls NA Affymetrix, Illumina [9848164] (imputed) 4 diverticulitis http://www.ebi.ac.uk/efo/EFO_1001460 GCST90293094 Genome-wide genotyping array 2023-10-06 37196047 Joo YY 2023-05-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/37196047 Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. Diverticulosis 19,211 European ancestry individuals NA Affymetrix, Illumina [9848164] (imputed) 3 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90293095 Genome-wide genotyping array 2023-10-06 37196047 Joo YY 2023-05-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/37196047 Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. Diverticulitis up to 19,211 European ancestry individuals NA Affymetrix, Illumina [9848164] (imputed) 2 diverticulitis http://www.ebi.ac.uk/efo/EFO_1001460 GCST90293096 Genome-wide genotyping array 2023-10-06 37196047 Joo YY 2023-05-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/37196047 Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. Diverticulosis 2,322 African ancestry individuals NA Affymetrix, Illumina [9848164] (imputed) 2 diverticular disease http://www.ebi.ac.uk/efo/EFO_0009959 GCST90293097 Genome-wide genotyping array 2023-10-06 37196047 Joo YY 2023-05-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/37196047 Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. Diverticulitis up to 2,322 African ancestry individuals NA Affymetrix, Illumina [9848164] (imputed) 13 diverticulitis http://www.ebi.ac.uk/efo/EFO_1001460 GCST90293098 Genome-wide genotyping array 2023-06-09 36580032 Rothwell S 2022-12-29 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36580032 Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies. Idiopathic inflammatory myopathy 2,565 European ancestry cases, 10,260 European ancestry controls NA Illumina [1648116] (imputed) 12 myositis http://www.ebi.ac.uk/efo/EFO_0000783 GCST90270216 Genome-wide genotyping array 2023-06-09 36580032 Rothwell S 2022-12-29 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36580032 Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies. Polymyositis 903 European ancestry cases, 10,260 European ancestry controls NA Illumina [1648116] (imputed) 7 polymyositis http://www.ebi.ac.uk/efo/EFO_0003063 GCST90270217 Genome-wide genotyping array 2023-06-09 36580032 Rothwell S 2022-12-29 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36580032 Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies. Dermatomyositis 817 European ancestry cases, 10,260 European ancestry controls NA Illumina [1648116] (imputed) 2 dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000398 GCST90270218 Genome-wide genotyping array 2023-06-09 36580032 Rothwell S 2022-12-29 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36580032 Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies. Juvenile dermatomyositis 508 European ancestry cases, 10,260 European ancestry controls NA Illumina [1648116] (imputed) 2 juvenile dermatomyositis http://www.ebi.ac.uk/efo/EFO_0000557 GCST90270219 Genome-wide genotyping array 2023-06-09 36580032 Rothwell S 2022-12-29 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36580032 Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies. Inclusion body myositis 252 European ancestry cases, 10,260 European ancestry controls NA Illumina [1648116] (imputed) 5 inclusion body myositis http://www.ebi.ac.uk/efo/EFO_0007323 GCST90270220 Genome-wide genotyping array 2023-06-09 36580032 Rothwell S 2022-12-29 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/36580032 Genome-wide imputation identifies novel associations and localises signals in idiopathic inflammatory myopathies. Idiopathic inflammatory myopathy with anti-Jo1 positive 311 European ancestry cases, 10,260 European ancestry controls NA Illumina [1648116] (imputed) 2 myositis, autoantibody measurement http://www.ebi.ac.uk/efo/EFO_0000783, http://www.ebi.ac.uk/efo/EFO_0004866 GCST90270221 Genome-wide genotyping array 2023-04-03 35760791 Blair DR 2022-06-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35760791 Common genetic variation associated with Mendelian disease severity revealed through cryptic phenotype analysis. Cryptic phenotype that captures hereditary hemorrhagic telangiectasia severity 308,381 European ancestry individuals NA Affymetrix [579430] 0 cryptic phenotype measurement http://www.ebi.ac.uk/efo/EFO_0021487 GCST90101826 Genome-wide genotyping array 2023-04-03 35760791 Blair DR 2022-06-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35760791 Common genetic variation associated with Mendelian disease severity revealed through cryptic phenotype analysis. Cryptic phenotype that captures Marfan syndrome severity 308,350 European ancestry individuals NA Affymetrix [579430] 0 cryptic phenotype measurement http://www.ebi.ac.uk/efo/EFO_0021487 GCST90101827 Genome-wide genotyping array 2023-04-03 35760791 Blair DR 2022-06-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35760791 Common genetic variation associated with Mendelian disease severity revealed through cryptic phenotype analysis. Cryptic phenotype that captures Alport syndrome severity 308,088 European ancestry individuals NA Affymetrix [579430] 3 cryptic phenotype measurement http://www.ebi.ac.uk/efo/EFO_0021487 GCST90101828 Genome-wide genotyping array 2023-04-03 35760791 Blair DR 2022-06-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35760791 Common genetic variation associated with Mendelian disease severity revealed through cryptic phenotype analysis. Cryptic phenotype that captures autosomal dominant polycystic kidney disease severity 308,095 European ancestry individuals NA Affymetrix [579430] 30 cryptic phenotype measurement http://www.ebi.ac.uk/efo/EFO_0021487 GCST90101829 Genome-wide genotyping array 2023-04-03 35760791 Blair DR 2022-06-27 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35760791 Common genetic variation associated with Mendelian disease severity revealed through cryptic phenotype analysis. Cryptic phenotype that captures alpha-1-antitrypsin deficiency severity 294,133 European ancestry individuals NA Affymetrix [579429] 3 cryptic phenotype measurement http://www.ebi.ac.uk/efo/EFO_0021487 GCST90101825 Genome-wide genotyping array 2023-04-14 36273105 Berndt SI 2022-10-22 Leukemia www.ncbi.nlm.nih.gov/pubmed/36273105 Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes. Non-Hodgkin lymphoma subtypes (chronic lymphocytic leukemia, diffuse large B-cell lymphoma, follicular lymphoma, or marginal zone lymphoma) (pleiotropy) 3,100 European ancestry chronic lymphocytic leukemia cases, 3,857 European ancestry diffuse large B-cell lymphoma cases, 2,847 European ancestry follicular lymphoma cases, 825 European ancestry marginal zone lymphoma cases, 9,505 European ancestry controls 1,404 European ancestry chronic lymphocytic leukemia cases, 1,259 European ancestry diffuse large B-cell lymphoma cases, 1,351 European ancestry follicular lymphoma cases, 454 European ancestry marginal zone lymphoma cases, 2,185 European ancestry controls Affymetrix, Illumina [8000000] (imputed) 2 diffuse large B-cell lymphoma, marginal zone B-cell lymphoma, follicular lymphoma, chronic lymphocytic leukemia http://www.ebi.ac.uk/efo/EFO_0000403, http://www.ebi.ac.uk/efo/EFO_1000630, http://purl.obolibrary.org/obo/MONDO_0018906, http://www.ebi.ac.uk/efo/EFO_0000095 GCST90267402 Genome-wide genotyping array 2023-04-14 36273105 Berndt SI 2022-10-22 Leukemia www.ncbi.nlm.nih.gov/pubmed/36273105 Distinct germline genetic susceptibility profiles identified for common non-Hodgkin lymphoma subtypes. Malignant lymphoma (Non-Hodgkin lymphoma, multiple myeloma, or Hodgkin lymphoma) 13,763 European ancestry cases, 18,862 European ancestry controls NA Affymetrix, Illumina [8000000] (imputed) 15 Hodgkins lymphoma, multiple myeloma, non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0000183, http://www.ebi.ac.uk/efo/EFO_0001378, http://www.ebi.ac.uk/efo/EFO_0005952 GCST90267403 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Rheumatoid factor [Units/volume] in Serum or Plasma 3,726 European ancestry individuals NA Illumina [6240610] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90012732 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Folate [Mass/volume] in Red Blood Cells 4,409 European ancestry individuals NA Illumina [6240610] (imputed) 0 folic acid measurement http://www.ebi.ac.uk/efo/EFO_0005111 GCST90012733 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Erythrocyte distribution width [Ratio] by Automated count Erythrocyte distribution width [Ratio] by Automated count 64,874 European ancestry individuals NA Illumina [6240610] (imputed) 0 Red cell distribution width http://www.ebi.ac.uk/efo/EFO_0009188 GCST90012734 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Erythrocyte distribution width [Entitic volume] by Automated count 57,768 European ancestry individuals NA Illumina [6240610] (imputed) 0 Red cell distribution width http://www.ebi.ac.uk/efo/EFO_0009188 GCST90012735 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Hemoglobin [Entitic mass] in Reticulocytes 4,543 European ancestry individuals NA Illumina [6240610] (imputed) 0 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90012736 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Reticulocytes/100 erythrocytes in Blood by Automated count 7,077 European ancestry individuals NA Illumina [6240610] (imputed) 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90012737 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Dilute Russell Viper Venom Time (dRVVT) actual/normal (normalized lupus anticoagulant (LA) screen) 1,876 European ancestry individuals NA Illumina [6240610] (imputed) 0 autoimmune disease http://www.ebi.ac.uk/efo/EFO_0005140 GCST90012738 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. SCL-70 extractable nuclear Ab [Units/volume] in Serum by Immunoassay 1,041 European ancestry individuals NA Illumina [6240610] (imputed) 0 anti-topoisomerase I antibody positivity http://www.ebi.ac.uk/efo/EFO_0803353 GCST90012740 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Erythrocyte sedimentation rate by Westergren method 10,541 European ancestry individuals NA Illumina [6240610] (imputed) 0 blood sedimentation http://www.ebi.ac.uk/efo/EFO_0004304 GCST90012741 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Folate [Mass/volume] in Serum or Plasma 5,998 European ancestry individuals NA Illumina [6240610] (imputed) 0 folic acid measurement http://www.ebi.ac.uk/efo/EFO_0005111 GCST90012742 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Creatinine [Mass/volume] in 24 hour Urine 1,487 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90012744 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Urea nitrogen [Mass/volume] in Urine 2,571 European ancestry individuals NA Illumina [6240610] (imputed) 0 urinary nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0005190 GCST90012745 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Creatinine [Mass/volume] in Urine 8,095 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90012746 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. T wave axis.horizontal plane Reference beat from EKG 6,818 European ancestry individuals NA Illumina [6240610] (imputed) 0 T wave duration http://www.ebi.ac.uk/efo/EFO_0011034 GCST90012747 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Absolute neutrophil count 25,118 European ancestry individuals NA Illumina [6240610] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90012709 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cholesterol.total/Cholesterol in HDL [Molar ratio] in Serum or Plasma 3,676 European ancestry individuals NA Illumina [6240610] (imputed) 0 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90012750 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Oxygen saturation Calculated from oxygen partial pressure in Venous blood 7,487 European ancestry individuals NA Illumina [6240610] (imputed) 0 oxygen saturation measurement http://www.ebi.ac.uk/efo/EFO_0005682 GCST90012711 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Volume in Urine collected for unspecified duration 5,007 European ancestry individuals NA Illumina [6240610] (imputed) 0 urine volume measurement http://www.ebi.ac.uk/efo/EFO_0010604 GCST90012752 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. P wave axis horizontal plane Reference beat from EKG 6,448 European ancestry individuals NA Illumina [6240610] (imputed) 0 P wave duration http://www.ebi.ac.uk/efo/EFO_0005094 GCST90012713 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Hematocrit [Volume Fraction] of Blood by Automated count 65,907 European ancestry individuals NA Illumina [6240610] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90012714 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. pH of Arterial blood 16,918 European ancestry individuals NA Illumina [6240610] (imputed) 0 urinary pH measurement http://www.ebi.ac.uk/efo/EFO_0010136 GCST90012715 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Troponin T.cardiac [Mass/volume] in Serum or Plasma 1,296 European ancestry individuals NA Illumina [6240610] (imputed) 0 cardiac troponin T measurement http://www.ebi.ac.uk/efo/EFO_0005043 GCST90012757 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Phosphate 17,359 European ancestry individuals NA Illumina [6240610] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90012717 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Oxygen [Partial pressure] in Arterial blood 7,536 European ancestry individuals NA Illumina [6240610] (imputed) 0 partial pressure of oxygen measurement http://www.ebi.ac.uk/efo/EFO_0803351 GCST90012718 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Hemoglobin A1c (Glycated) 3,276 European ancestry individuals NA Illumina [6240610] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90012719 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. PP interval mean 6,693 European ancestry individuals NA Illumina [6240610] (imputed) 0 PP interval http://www.ebi.ac.uk/efo/EFO_0600085 GCST90012720 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Prealbumin [Mass/volume] in Serum or Plasma 6,502 European ancestry individuals NA Illumina [6240610] (imputed) 0 prealbumin measurement http://www.ebi.ac.uk/efo/EFO_0803352 GCST90012721 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Prolactin [Mass/volume] in Serum or Plasma 2,705 European ancestry individuals NA Illumina [6240610] (imputed) 0 prolactin measurement http://www.ebi.ac.uk/efo/EFO_0007003 GCST90012722 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. PSA serum/plasma 7,837 European ancestry individuals NA Illumina [6240610] (imputed) 0 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST90012723 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. International normalized ratio (INR) 34,919 European ancestry individuals NA Illumina [6240610] (imputed) 0 prothrombin time measurement http://www.ebi.ac.uk/efo/EFO_0008390 GCST90012724 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Nucleated cells [#/volume] in Synovial fluid by Manual count 1,665 European ancestry individuals NA Illumina [6240610] (imputed) 0 nucleated cell count http://www.ebi.ac.uk/efo/EFO_0803347 GCST90012656 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Iron [Mass/volume] in Serum or Plasma 15,335 European ancestry individuals NA Illumina [6240610] (imputed) 0 serum iron measurement http://www.ebi.ac.uk/efo/EFO_0006332 GCST90012683 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Lactate [Moles/volume] in Serum or Plasma 9,679 European ancestry individuals NA Illumina [6240610] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90012684 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cholesterol in LDL [Mass/volume] in Serum or Plasma by calculation 28,417 European ancestry individuals NA Illumina [6240610] (imputed) 0 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90012685 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. LEUKOREDUCED_RANDOM_PLATELETS 2,124 European ancestry individuals NA Illumina [6240610] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90012686 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Lutropin [Units/volume] in Serum or Plasma 2,133 European ancestry individuals NA Illumina [6240610] (imputed) 0 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90012687 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Lipemic index of Serum or Plasma 4,500 European ancestry individuals NA Illumina [6240610] (imputed) 0 lipemic index http://www.ebi.ac.uk/efo/EFO_0803349 GCST90012688 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Lymphocytes Count [#/volume] in Blood 26,179 European ancestry individuals NA Illumina [6240610] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90012689 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Lymphocytes Count [#/volume] in Blood by Automated count 25,135 European ancestry individuals NA Illumina [6240610] (imputed) 0 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90012690 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Lymphocytes/100 leukocytes in Blood by Automated count 46,503 European ancestry individuals NA Illumina [6240610] (imputed) 0 lymphocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007993 GCST90012691 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Creatine kinase.MB/Creatine kinase.total in Serum or Plasma 13,080 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST90012692 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. MCH [Entitic mass] by Automated count 64,869 European ancestry individuals NA Illumina [6240610] (imputed) 0 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90012693 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. MCHC [Mass/volume] by Automated count 54,231 European ancestry individuals NA Illumina [6240610] (imputed) 0 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90012694 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. MCV [Entitic volume] by Automated count 64,844 European ancestry individuals NA Illumina [6240610] (imputed) 0 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90012695 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Magnesium [Mass/volume] in Serum or Plasma 20,707 European ancestry individuals NA Illumina [6240610] (imputed) 0 magnesium measurement http://www.ebi.ac.uk/efo/EFO_0004845 GCST90012696 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Absolute monocyte count 25,130 European ancestry individuals NA Illumina [6240610] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90012697 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Bicarbonate [Moles/volume] in Unspecified specimen 16,640 European ancestry individuals NA Illumina [6240610] (imputed) 0 blood bicarbonate measurement http://www.ebi.ac.uk/efo/EFO_0011012 GCST90012670 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Monocytes/100 leukocytes in Blood by Manual count 10,295 European ancestry individuals NA Illumina [6240610] (imputed) 0 monocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007989 GCST90012699 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Monocytes/100 leukocytes in Blood by Automated count 46,569 European ancestry individuals NA Illumina [6240610] (imputed) 0 monocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007989 GCST90012700 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Platelet mean volume [Entitic volume] in Blood by Automated count 46,661 European ancestry individuals NA Illumina [6240610] (imputed) 0 mean platelet volume http://www.ebi.ac.uk/efo/EFO_0004584 GCST90012701 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Myelocytes/100 leukocytes in Blood by Manual count 7,452 European ancestry individuals NA Illumina [6240610] (imputed) 0 neutrophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007990 GCST90012702 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Collection duration of Unspecified specimen 1,555 European ancestry individuals NA Illumina [6240610] (imputed) 0 urine volume measurement http://www.ebi.ac.uk/efo/EFO_0010604 GCST90012676 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Polymorphonuclear cells/100 leukocytes in Body fluid by Manual count 10,371 European ancestry individuals NA Illumina [6240610] (imputed) 0 granulocyte count http://www.ebi.ac.uk/efo/EFO_0007987 GCST90012704 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Neutrophils/100 leukocytes in Blood by Automated count 46,596 European ancestry individuals NA Illumina [6240610] (imputed) 0 neutrophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007990 GCST90012705 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. IgG [Mass/volume] in Serum or Plasma 3,471 European ancestry individuals NA Illumina [6240610] (imputed) 0 serum IgG measurement http://www.ebi.ac.uk/efo/EFO_0004565 GCST90012679 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cholesterol [Mass/volume] in Serum or Plasma 30,388 European ancestry individuals NA Illumina [6240610] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90012628 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cardiolipin IgA Ab [Units/volume] in Serum by Immunoassay 1,908 European ancestry individuals NA Illumina [6240610] (imputed) 0 cardiolipin IgA antibody measurement http://www.ebi.ac.uk/efo/EFO_0803340 GCST90012604 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Chloride [Moles/volume] in Blood 6,828 European ancestry individuals NA Illumina [6240610] (imputed) 0 chloride measurement http://www.ebi.ac.uk/efo/EFO_0009284 GCST90012630 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Corticotropin [Mass/volume] in Plasma 1,486 European ancestry individuals NA Illumina [6240610] (imputed) 0 corticotropin measurement http://www.ebi.ac.uk/efo/EFO_0020289 GCST90012606 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Albumin [Presence] in Urine 5,255 European ancestry individuals NA Illumina [6240610] (imputed) 0 urinary albumin excretion rate http://www.ebi.ac.uk/efo/EFO_0005667 GCST90012607 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Neutrophils/100 leukocytes in Cerebral spinal fluid by Manual count 1,680 European ancestry individuals NA Illumina [6240610] (imputed) 0 neutrophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007990 GCST90012632 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Carbon dioxide serum/plasma 62,304 European ancestry individuals NA Illumina [6240610] (imputed) 0 carbon dioxide measurement http://www.ebi.ac.uk/efo/EFO_0803345 GCST90012633 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Carboxyhemoglobin % in blood 6,491 European ancestry individuals NA Illumina [6240610] (imputed) 0 carboxyhemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0803346 GCST90012634 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cortisol [Mass/volume] in Serum or Plasma 6,342 European ancestry individuals NA Illumina [6240610] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90012635 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. CPK 16,742 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST90012636 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Basophils Count [#/volume] in Blood by Automated count 24,660 European ancestry individuals NA Illumina [6240610] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90012614 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Basophils Count [#/volume] in Blood 25,520 European ancestry individuals NA Illumina [6240610] (imputed) 0 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90012615 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Basophils/100 leukocytes in Blood by Manual count 7,802 European ancestry individuals NA Illumina [6240610] (imputed) 0 basophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007992 GCST90012616 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Vitamin D [Mass/volume] in Serum or Plasma 18,315 European ancestry individuals NA Illumina [6240610] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90012641 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cholesterol in LDL [Mass/volume] in Serum or Plasma by Direct assay 4,859 European ancestry individuals NA Illumina [6240610] (imputed) 0 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90012643 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Eosinophils absolute count 24,652 European ancestry individuals NA Illumina [6240610] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90012645 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Complement C3 [Mass/volume] in Serum or Plasma 3,672 European ancestry individuals NA Illumina [6240610] (imputed) 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90012620 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Eosinophils [#/volume] in Blood by Automated count 30,322 European ancestry individuals NA Illumina [6240610] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90012647 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Eosinophils/100 leukocytes in Blood by Automated count 32,924 European ancestry individuals NA Illumina [6240610] (imputed) 0 eosinophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007991 GCST90012649 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Bilirubin.conjugated [Mass/volume] in Serum or Plasma 23,850 European ancestry individuals NA Illumina [6240610] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90012624 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Fibrinogen [Mass/volume] in Platelet poor plasma by Coagulation assay 5,854 European ancestry individuals NA Illumina [6240610] (imputed) 0 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90012651 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Eosinophils/100 leukocytes in Body fluid by Manual count 1,582 European ancestry individuals NA Illumina [6240610] (imputed) 0 eosinophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007991 GCST90012652 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Ferritin [Mass/volume] in Serum or Plasma 16,215 European ancestry individuals NA Illumina [6240610] (imputed) 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90012653 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Tacrolimus [Mass/volume] in Blood 1,568 European ancestry individuals NA Illumina [6240610] (imputed) 0 tacrolimus measurement http://www.ebi.ac.uk/efo/EFO_0008458 GCST90012654 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Mononuclear cells [#/volume] in Body fluid by Manual count 1,761 European ancestry individuals NA Illumina [6240610] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90012655 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Immature reticulocytes/Reticulocytes.total in Blood 5,554 European ancestry individuals NA Illumina [6240610] (imputed) 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90012682 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. FRONTAL AXIS INITIAL 40 MS from EKG 6,835 European ancestry individuals NA Illumina [6240610] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90012657 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. P wave axis from EKG 6,581 European ancestry individuals NA Illumina [6240610] (imputed) 0 P wave duration http://www.ebi.ac.uk/efo/EFO_0005094 GCST90012658 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. ST segment axis.horizontal plane 6,914 European ancestry individuals NA Illumina [6240610] (imputed) 0 ST segment duration http://www.ebi.ac.uk/efo/EFO_0011033 GCST90012659 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. FRONTAL AXIS TERMINAL 40 MS from EKG 6,902 European ancestry individuals NA Illumina [6240610] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90012660 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Follitropin [Units/volume] in Serum or Plasma 3,484 European ancestry individuals NA Illumina [6240610] (imputed) 0 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90012661 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Thyroxine (T4) free [Mass/volume] in Serum or Plasma 26,231 European ancestry individuals NA Illumina [6240610] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90012662 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cells Counted Total [#] in Body fluid 2,938 European ancestry individuals NA Illumina [6240610] (imputed) 0 complete blood cell count http://www.ebi.ac.uk/efo/EFO_0004586 GCST90012663 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Glucose [Mass/volume] in Blood by Automated test strip 25,193 European ancestry individuals NA Illumina [6240610] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90012664 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Glucose 62,341 European ancestry individuals NA Illumina [6240610] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90012665 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Glucose [Mass/volume] in Blood 13,848 European ancestry individuals NA Illumina [6240610] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90012666 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Glucose tolerance test 1 hour, 50 g (GTT50g) 2,353 European ancestry individuals NA Illumina [6240610] (imputed) 0 glucose tolerance test http://www.ebi.ac.uk/efo/EFO_0004307 GCST90012667 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Haptoglobin [Mass/volume] in Serum or Plasma 2,437 European ancestry individuals NA Illumina [6240610] (imputed) 0 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90012668 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Hepatitis B virus surface Ab [Presence] in Serum 2,255 European ancestry individuals NA Illumina [6240610] (imputed) 0 Hepatitis B virus surface antigen seropositivity http://www.ebi.ac.uk/efo/EFO_0009345 GCST90012669 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Monocytes [#/volume] in Blood by Manual count 26,166 European ancestry individuals NA Illumina [6240610] (imputed) 0 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90012698 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Hematocrit 12,434 European ancestry individuals NA Illumina [6240610] (imputed) 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90012671 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cholesterol in HDL [Mass/volume] in Serum or Plasma 29,497 European ancestry individuals NA Illumina [6240610] (imputed) 0 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90012672 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Hemoglobin A1c (Glycated) 21,558 European ancestry individuals NA Illumina [6240610] (imputed) 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90012673 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. QRS axis from EKG 6,793 European ancestry individuals NA Illumina [6240610] (imputed) 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90012675 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Neutrophils [#/volume] in Blood 26,402 European ancestry individuals NA Illumina [6240610] (imputed) 0 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90012703 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Icteric index of Serum or Plasma 4,493 European ancestry individuals NA Illumina [6240610] (imputed) 0 icteric index http://www.ebi.ac.uk/efo/EFO_0803348 GCST90012677 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. IgA [Mass/volume] in Serum or Plasma 7,677 European ancestry individuals NA Illumina [6240610] (imputed) 0 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST90012678 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cholesterol non HDL [Mass/volume] in Serum or Plasma 3,252 European ancestry individuals NA Illumina [6240610] (imputed) 0 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90012706 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Immature granulocytes/100 leukocytes in Blood 44,827 European ancestry individuals NA Illumina [6240610] (imputed) 0 granulocyte percentage of myeloid white cells http://www.ebi.ac.uk/efo/EFO_0007997 GCST90012680 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Platelets reticulated/100 platelets in Blood by Automated count 4,608 European ancestry individuals NA Illumina [6240610] (imputed) 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90012681 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Alpha 1 antitrypsin [Mass/volume] in Serum or Plasma 1,756 European ancestry individuals NA Illumina [6240610] (imputed) 0 alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008327 GCST90012603 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Creatine kinase.MB [Mass/volume] in Serum or Plasma 13,294 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST90012629 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cardiolipin IgM Ab [Units/volume] in Serum by Immunoassay 2,162 European ancestry individuals NA Illumina [6240610] (imputed) 0 cardiolipin IgM antibody measurement http://www.ebi.ac.uk/efo/EFO_0803341 GCST90012605 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Lymphocytes/100 leukocytes in Cerebral spinal fluid by Manual count 2,091 European ancestry individuals NA Illumina [6240610] (imputed) 0 lymphocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007993 GCST90012631 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Microalbumin/Creatinine [Mass Ratio] in 24 hour Urine 2,935 European ancestry individuals NA Illumina [6240610] (imputed) 0 urinary albumin to creatinine ratio http://www.ebi.ac.uk/efo/EFO_0007778 GCST90012608 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Aldosterone [Mass/volume] in Serum or Plasma 1,128 European ancestry individuals NA Illumina [6240608] (imputed) 0 aldosterone measurement http://www.ebi.ac.uk/efo/EFO_0010219 GCST90012609 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Ammonia [Moles/volume] in Plasma 3,059 European ancestry individuals NA Illumina [6240610] (imputed) 0 ammonia measurement http://www.ebi.ac.uk/efo/EFO_0803342 GCST90012610 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Amylase [Enzymatic activity/volume] in Serum or Plasma 8,067 European ancestry individuals NA Illumina [6240610] (imputed) 0 amylase measurement http://www.ebi.ac.uk/efo/EFO_0803343 GCST90012611 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Anion gap serum/plasma 62,164 European ancestry individuals NA Illumina [6240610] (imputed) 0 anion gap measurement http://www.ebi.ac.uk/efo/EFO_0803344 GCST90012612 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. P wave Atrium by EKG 6,933 European ancestry individuals NA Illumina [6240610] (imputed) 0 P wave duration http://www.ebi.ac.uk/efo/EFO_0005094 GCST90012613 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Creatine kinase [Enzymatic activity/volume] in Serum or Plasma 7,585 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatine kinase measurement http://www.ebi.ac.uk/efo/EFO_0004534 GCST90012637 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Protein [Mass/volume] in Cerebral spinal fluid 2,795 European ancestry individuals NA Illumina [6240610] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90012638 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Creatinine [Mass/volume] in Blood Creatinine [Mass/volume] in Blood 62,909 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90012639 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. C reactive protein [Mass/volume] in Serum or Plasma 20,008 European ancestry individuals NA Illumina [6240610] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90012640 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Basophils/100 leukocytes in Blood by Automated count 46,524 European ancestry individuals NA Illumina [6240610] (imputed) 0 basophil percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007992 GCST90012617 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Natriuretic peptide B [Mass/volume] in Serum or Plasma 11,374 European ancestry individuals NA Illumina [6240610] (imputed) 0 natriuretic peptides B measurement http://www.ebi.ac.uk/efo/EFO_0010628 GCST90012618 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Urea nitrogen serum/plasma 62,403 European ancestry individuals NA Illumina [6240610] (imputed) 0 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST90012619 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Eosinophils 25,862 European ancestry individuals NA Illumina [6240610] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90012646 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Complement C4 [Mass/volume] in Serum or Plasma 3,667 European ancestry individuals NA Illumina [6240610] (imputed) 0 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST90012621 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Calcium serum/plasma serum/plasma 62,143 European ancestry individuals NA Illumina [6240610] (imputed) 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90012622 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Calcium.ionized [Mass/volume] in Blood 16,300 European ancestry individuals NA Illumina [6240610] (imputed) 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90012623 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Eosinophils % 30,313 European ancestry individuals NA Illumina [6240610] (imputed) 0 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90012650 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. CD19% 1,119 European ancestry individuals NA Illumina [6240607] (imputed) 0 CD19-positive B-lymphocyte count http://www.ebi.ac.uk/efo/EFO_0010108 GCST90012625 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. CD3+CD4+ (T4 helper) cells/100 cells in Blood 1,673 European ancestry individuals NA Illumina [6240610] (imputed) 0 CD4-positive T-lymphocyte count, CD3-positive T-lymphocyte count http://www.ebi.ac.uk/efo/EFO_0010105, http://www.ebi.ac.uk/efo/EFO_0010106 GCST90012626 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. CD3+CD4+ (T4 helper) cells [#/volume] in Blood 1,551 European ancestry individuals NA Illumina [6240610] (imputed) 0 CD4-positive T-lymphocyte count, CD3-positive T-lymphocyte count http://www.ebi.ac.uk/efo/EFO_0010105, http://www.ebi.ac.uk/efo/EFO_0010106 GCST90012627 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Nucleated erythrocytes [#/volume] in Blood by Automated count 1,860 European ancestry individuals NA Illumina [6240610] (imputed) 0 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90012707 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Parathyrin.intact [Mass/volume] in Serum or Plasma 6,708 European ancestry individuals NA Illumina [6240610] (imputed) 0 intact parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0803350 GCST90012708 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. T wave axis from EKG 6,912 European ancestry individuals NA Illumina [6240610] (imputed) 0 T wave duration http://www.ebi.ac.uk/efo/EFO_0011034 GCST90012748 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Total Bilirubin serum/plasma 56,577 European ancestry individuals NA Illumina [6240610] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90012749 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Oxygen Saturation 8,017 European ancestry individuals NA Illumina [6240610] (imputed) 0 oxygen saturation measurement http://www.ebi.ac.uk/efo/EFO_0005682 GCST90012710 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Testosterone Free [Mass/volume] in Serum or Plasma 1,830 European ancestry individuals NA Illumina [6240610] (imputed) 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90012751 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Osmolality of Serum or Plasma 1,788 European ancestry individuals NA Illumina [6240610] (imputed) 0 blood osmolality measurement http://www.ebi.ac.uk/efo/EFO_0007967 GCST90012712 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Protein serum/plasma 32,127 European ancestry individuals NA Illumina [6240610] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90012753 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Tau protein [Presence] in Body fluid 44,329 European ancestry individuals NA Illumina [6240610] (imputed) 0 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST90012754 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Triglyceride [Mass/volume] in Serum or Plasma 30,597 European ancestry individuals NA Illumina [6240610] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90012755 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Transferrin [Mass/volume] in Serum or Plasma 1,781 European ancestry individuals NA Illumina [6240610] (imputed) 0 transferrin measurement http://www.ebi.ac.uk/efo/EFO_0006341 GCST90012756 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. pH of Venous blood 8,460 European ancestry individuals NA Illumina [6240610] (imputed) 0 urinary pH measurement http://www.ebi.ac.uk/efo/EFO_0010136 GCST90012716 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Troponin I.cardiac [Mass/volume] in Serum or Plasma 10,443 European ancestry individuals NA Illumina [6240610] (imputed) 0 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST90012758 Genome-wide genotyping array 2023-05-16 34651315 Fairfield CJ 2021-12-10 Hepatology www.ncbi.nlm.nih.gov/pubmed/34651315 Genome-wide analysis identifies gallstone-susceptibility loci including genes regulating gastrointestinal motility. Gallstone disease 43,639 European ancestry cases, 506,798 European ancestry controls 1,089 cases, 5,228 controls Affymetrix, Illumina [10044759] (imputed) 64 gallstones http://www.ebi.ac.uk/efo/EFO_0004210 GCST90128518 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Frontal QRS-T angle 159,715 European ancestry, African ancestry, Hispanic or Latin American individuals NA Affymetrix, Illumina [8299259] (imputed) 11 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246319 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Spatial QRS-T angle 96,562 European ancestry individuals NA Affymetrix, Illumina [8603009] (imputed) 51 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246320 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Spatial QRS-T angle 118,780 European ancestry, African ancestry, Hispanic or Latin American individuals NA Affymetrix, Illumina [9052360] (imputed) 61 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246318 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Frontal QRS-T angle 134,567 European ancestry individuals NA Affymetrix, Illumina [7954211] (imputed) 9 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246321 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Spatial QRS-T angle 8,351 African ancestry individuals NA Affymetrix, Illumina [16110045] (imputed) 1 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246322 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Frontal QRS-T angle 10,772 African ancestry individuals NA Affymetrix, Illumina [15436228] (imputed) 1 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246323 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Spatial QRS-T angle 12,652 Hispanic or Latin American individuals NA Affymetrix, Illumina [11748645] (imputed) 2 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246324 Genome-wide genotyping array 2023-05-12 36918541 Young WJ 2023-03-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36918541 Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease. Frontal QRS-T angle 12,652 Hispanic or Latin American individuals NA Affymetrix, Illumina [11748645] (imputed) 0 QRS-T angle http://www.ebi.ac.uk/efo/EFO_0020097 GCST90246325 Genome-wide genotyping array 2023-05-16 36708065 Eektimmerman F 2023-01-27 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36708065 Genome-wide association study of methotrexate-induced liver injury in rheumatoid arthritis patients. Methotrexate-induced liver injury in rheumatoid arthritis 108 European ancestry cases, 311 European ancestry controls NA Illumina [502291] (imputed) 7 response to methotrexate, drug-induced liver injury http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004228 GCST90269900 Genome-wide genotyping array 2023-05-16 36708065 Eektimmerman F 2023-01-27 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/36708065 Genome-wide association study of methotrexate-induced liver injury in rheumatoid arthritis patients. Methotrexate-induced liver injury in rheumatoid arthritis 108 European ancestry cases, 311 European ancestry controls NA Illumina [9328966] (imputed) 18 response to methotrexate, drug-induced liver injury http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004228 GCST90269901 Genome-wide genotyping array 2023-07-17 37285119 Tyrmi JS 2023-06-07 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/37285119 Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. Preeclampsia (maternal genotype effect) 16,743 European ancestry cases, 280,081 European ancestry controls, 16,743 Central Asian ancestry cases, 280,081 Central Asian ancestry controls NA Affymetrix, Illumina [15190084] (imputed) 9 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90269903 Genome-wide genotyping array 2023-07-17 37285119 Tyrmi JS 2023-06-07 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/37285119 Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. Preeclampsia or other maternal hypertension (maternal genotype effect) 15,200 European ancestry cases, 115,007 European ancestry controls NA Affymetrix, Illumina [14417327] (imputed) 13 preeclampsia, hypertension, pregnancy-induced http://www.ebi.ac.uk/efo/EFO_0000668, http://purl.obolibrary.org/obo/MONDO_0024664 GCST90269904 Genome-wide genotyping array 2023-07-17 37285119 Tyrmi JS 2023-06-07 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/37285119 Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. Preeclampsia or small for gestational age infant (maternal genotype effect) 10,800 European ancestry cases, 119,225 European ancestry controls NA Affymetrix, Illumina [14441767] (imputed) 2 Small for gestational age, preeclampsia http://purl.obolibrary.org/obo/HP_0001518, http://www.ebi.ac.uk/efo/EFO_0000668 GCST90269905 Genome-wide genotyping array 2023-07-17 37285119 Tyrmi JS 2023-06-07 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/37285119 Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. Preeclampsia (fetal genotype effect) 796 European ancestry cases, 894 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 5 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90270941 Genome-wide genotyping array 2023-07-17 37285119 Tyrmi JS 2023-06-07 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/37285119 Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. Preeclampsia or other maternal hypertension (fetal genotype effect) 946 European ancestry cases, 750 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 preeclampsia, hypertension, pregnancy-induced http://www.ebi.ac.uk/efo/EFO_0000668, http://purl.obolibrary.org/obo/MONDO_0024664 GCST90270942 Genome-wide genotyping array 2023-07-17 37285119 Tyrmi JS 2023-06-07 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/37285119 Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. Preeclampsia (paternal genotype effect) 595 European ancestry cases, 654 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 6 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90270943 Genome-wide genotyping array 2023-07-17 37285119 Tyrmi JS 2023-06-07 JAMA Cardiol www.ncbi.nlm.nih.gov/pubmed/37285119 Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. Preeclampsia or other maternal hypertension (paternal genotype effect) 697 European ancestry cases, 557 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 preeclampsia, hypertension, pregnancy-induced http://www.ebi.ac.uk/efo/EFO_0000668, http://purl.obolibrary.org/obo/MONDO_0024664 GCST90270944 Genome-wide genotyping array 2023-03-29 36922633 Teder-Laving M 2023-03-16 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36922633 Genome-wide meta-analysis identifies novel loci conferring risk of acne vulgaris. acne vulgaris 34,422 European ancestry cases, 364,991 European ancestry controls NA Affymetrix, Illumina [6438339] (imputed) 46 acne http://www.ebi.ac.uk/efo/EFO_0003894 GCST90245818 Genome-wide genotyping array 2023-08-02 36996866 Choi CK 2023-03-22 Epidemiol Health www.ncbi.nlm.nih.gov/pubmed/36996866 No association between C-reactive protein and colorectal cancer survival: Two-sample Mendelian randomization analysis. C-reactive protein levels 47,258 Korean ancestry individuals 12,480 Korean ancestry individuals NR [6211142] (imputed) 7 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90275066 Genome-wide genotyping array 2023-05-26 36725857 Phelan J 2023-02-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36725857 Genome-wide host-pathogen analyses reveal genetic interaction points in tuberculosis disease. Tuberculosis x mycobacterium tuberculosis lineage interaction 714 East Asian ancestry cases NA Illumina [5948940] (imputed) 9 bacterial pathogen genotype measurement, pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_0010271, http://www.ebi.ac.uk/efo/EFO_1000049 GCST90270069 Genome-wide genotyping array 2023-05-26 36725857 Phelan J 2023-02-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36725857 Genome-wide host-pathogen analyses reveal genetic interaction points in tuberculosis disease. Tuberculosis (main host cluster) x mycobacterium tuberculosis lineage interaction 426 East Asian ancestry cases NA Illumina [5948940] (imputed) 3 bacterial pathogen genotype measurement, pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_0010271, http://www.ebi.ac.uk/efo/EFO_1000049 GCST90270070 Genome-wide genotyping array 2023-06-14 36720675 Han M 2023-01-05 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/36720675 Novel Genetic Variants Associated with Chronic Kidney Disease Progression. eGFR slope in chronic kidney disease 1,738 East Asian ancestry individuals 1,339 European ancestry individuals, 1,159 African American individuals NR [7734192] (imputed) 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90270264 Genome-wide genotyping array 2023-06-14 36720675 Han M 2023-01-05 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/36720675 Novel Genetic Variants Associated with Chronic Kidney Disease Progression. eGFR slope in diabetic chronic kidney disease 771 East Asian ancestry individuals 511 European ancestry individuals, 576 African American individuals NR [7734192] (imputed) 0 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90270265 Genome-wide genotyping array 2023-06-14 36720675 Han M 2023-01-05 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/36720675 Novel Genetic Variants Associated with Chronic Kidney Disease Progression. eGFR slope in non-diabetic chronic kidney disease 967 East Asian ancestry individuals 828 European ancestry individuals, 583 African American individuals NR [7734192] (imputed) 13 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90270266 Genome-wide genotyping array 2023-04-28 36649279 Shen Y 2023-01-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/36649279 Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population. COVID-19 124 European ancestry cases, 57 European ancestry controls NA NR [NR] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90268006 Genome-wide genotyping array 2023-04-28 36649279 Shen Y 2023-01-17 PLoS One www.ncbi.nlm.nih.gov/pubmed/36649279 Ancestral origins are associated with SARS-CoV-2 susceptibility and protection in a Florida patient population. COVID-19 80 African American cases, 11 African American controls NA NR [NR] (imputed) 0 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90268007 Genome-wide genotyping array 2023-05-11 35815403 Trejo MJ 2022-07-09 Nutr Cancer www.ncbi.nlm.nih.gov/pubmed/35815403 Genome-Wide Association Study of Metachronous Colorectal Adenoma Risk among Participants in the Selenium Trial. Metachronous colorectal adenoma 534 European ancestry cases, 681 European ancestry controls NA Illumina [5380949] (imputed) 10 metachronous colorectal adenoma http://www.ebi.ac.uk/efo/EFO_0803377 GCST90269770 Genome-wide genotyping array 2023-05-11 35815403 Trejo MJ 2022-07-09 Nutr Cancer www.ncbi.nlm.nih.gov/pubmed/35815403 Genome-Wide Association Study of Metachronous Colorectal Adenoma Risk among Participants in the Selenium Trial. Advanced metachronous adenoma 119 European ancestry cases, 681 European ancestry controls NA Illumina [5380949] (imputed) 12 metachronous colorectal adenoma http://www.ebi.ac.uk/efo/EFO_0803377 GCST90269771 Genome-wide genotyping array 2023-05-11 35815403 Trejo MJ 2022-07-09 Nutr Cancer www.ncbi.nlm.nih.gov/pubmed/35815403 Genome-Wide Association Study of Metachronous Colorectal Adenoma Risk among Participants in the Selenium Trial. Multiple metachronous adenoma 137 European ancestry cases, 681 European ancestry controls NA Illumina [5380949] (imputed) 9 metachronous colorectal adenoma http://www.ebi.ac.uk/efo/EFO_0803377 GCST90269772 Genome-wide genotyping array 2023-08-24 37432232 Park S 2023-04-26 Nutrients www.ncbi.nlm.nih.gov/pubmed/37432232 A Positive Causal Relationship between Noodle Intake and Metabolic Syndrome: A Two-Sample Mendelian Randomization Study. Noodle intake 58,701 Korean ancestry individuals NA Affymetrix [NR] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90278199 Genome-wide genotyping array 2023-03-23 36811574 Parlato LA 2022-12-23 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/36811574 Genome-wide association study (GWAS) of circulating vitamin D outcomes among individuals of African ancestry. Vitamin D-binding protein levels 2,602 African American individuals NA NR [2902059] (imputed) 4 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST90258654 Genome-wide genotyping array 2023-03-23 36811574 Parlato LA 2022-12-23 Am J Clin Nutr www.ncbi.nlm.nih.gov/pubmed/36811574 Genome-wide association study (GWAS) of circulating vitamin D outcomes among individuals of African ancestry. 25-Hydroxyvitamin D levels 6,934 African American or Afro-Caribbean individuals NA NR [11947647] (imputed) 1 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90258655 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Thyroxine (T4) [Mass/volume] in Serum or Plasma 4,023 European ancestry individuals NA Illumina [6240610] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90012759 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Tissue transglutaminase IgA Ab [Units/volume] in Serum by Immunoassay 1,558 European ancestry individuals NA Illumina [6240610] (imputed) 0 tissue transglutaminase IgA antibody measurement http://www.ebi.ac.uk/efo/EFO_0803354 GCST90012760 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Glucose urine dipstick 4,258 European ancestry individuals NA Illumina [6240610] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90012761 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Ketones [Mass/volume] in Urine by Test strip 5,842 European ancestry individuals NA Illumina [6240610] (imputed) 0 ketone body measurement http://www.ebi.ac.uk/efo/EFO_0010110 GCST90012762 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. pH of Urine by Test strip 40,674 European ancestry individuals NA Illumina [6240610] (imputed) 0 urinary pH measurement http://www.ebi.ac.uk/efo/EFO_0010136 GCST90012763 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Urate [Mass/volume] in Serum or Plasma 9,825 European ancestry individuals NA Illumina [6240610] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90012764 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Urobilinogen [Units/volume] in Urine by Test strip 4,040 European ancestry individuals NA Illumina [6240610] (imputed) 0 I-urobilinogen measurement http://www.ebi.ac.uk/efo/EFO_0800155 GCST90012765 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Protein [Mass/volume] in Urine by Test strip 17,649 European ancestry individuals NA Illumina [6240610] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90012766 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Specific gravity of Urine by Test strip 40,547 European ancestry individuals NA Illumina [6240610] (imputed) 0 urine specific gravity measurement http://www.ebi.ac.uk/efo/EFO_0010135 GCST90012767 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Urobilinogen [Presence] in Urine by Test strip 16,922 European ancestry individuals NA Illumina [6240610] (imputed) 0 I-urobilinogen measurement http://www.ebi.ac.uk/efo/EFO_0800155 GCST90012768 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Vancomycin [Mass/volume] in Serum or Plasma 7,342 European ancestry individuals NA Illumina [6240610] (imputed) 0 vancomycin trough measurement http://www.ebi.ac.uk/efo/EFO_0007648 GCST90012769 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Vancomycin [Susceptibility] by Minimum inhibitory concentration (MIC) 1,576 European ancestry individuals NA Illumina [6240610] (imputed) 0 vancomycin trough measurement http://www.ebi.ac.uk/efo/EFO_0007648 GCST90012770 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Vitamin D [Mass/volume] in Serum or Plasma 3,245 European ancestry individuals NA Illumina [6240610] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90012771 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Cobalamin (Vitamin B12) [Mass/volume] in Serum or Plasma 19,415 European ancestry individuals NA Illumina [6240610] (imputed) 0 vitamin B12 measurement http://www.ebi.ac.uk/efo/EFO_0004620 GCST90012772 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Retinol [Mass/volume] in Serum or Plasma 2,007 European ancestry individuals NA Illumina [6240610] (imputed) 0 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90012773 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Pyridoxine [Mass/volume] in Serum or Plasma 1,758 European ancestry individuals NA Illumina [6240610] (imputed) 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST90012774 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Leukocytes [#/volume] in Blood by Automated count 64,836 European ancestry individuals NA Illumina [6240610] (imputed) 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90012775 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Creatinine [Mass/volume] in Blood 6,900 European ancestry individuals NA Illumina [6240610] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90012776 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Troponin I.cardiac [Mass/volume] in Blood 1,819 European ancestry individuals NA Illumina [6240610] (imputed) 0 cardiac troponin I measurement http://www.ebi.ac.uk/efo/EFO_0010071 GCST90012777 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Calcitriol [Mass/volume] in Serum or Plasma 2,685 European ancestry individuals NA Illumina [6240610] (imputed) 0 calcitriol measurement http://www.ebi.ac.uk/efo/EFO_0803355 GCST90012779 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. 25-Hydroxyvitamin D2+25-Hydroxyvitamin D3 [Mass/volume] in Serum or Plasma 9,501 European ancestry individuals NA Illumina [6240610] (imputed) 0 25-hydroxyvitamin D2 measurement, 25-hydroxyvitamin D3 measurement http://www.ebi.ac.uk/efo/EFO_0803356, http://www.ebi.ac.uk/efo/EFO_0803357 GCST90012780 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. 25-Hydroxycalciferol [Mass/volume] in Serum or Plasma 2,877 European ancestry individuals NA Illumina [6240610] (imputed) 0 calcitriol measurement http://www.ebi.ac.uk/efo/EFO_0803355 GCST90012781 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Calcidiol [Mass/volume] in Serum or Plasma 9,523 European ancestry individuals NA Illumina [6240610] (imputed) 0 calcitriol measurement http://www.ebi.ac.uk/efo/EFO_0803355 GCST90012782 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Hemorheological index (nd1 levels) 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 1 hemorheological measurement http://www.ebi.ac.uk/efo/EFO_0803374 GCST90255653 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Hemorheological index (nd30 levels) 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 2 hemorheological measurement http://www.ebi.ac.uk/efo/EFO_0803374 GCST90255654 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Hemorheological index (nd300 levels) 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 3 hemorheological measurement http://www.ebi.ac.uk/efo/EFO_0803374 GCST90255655 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Relative index of whole blood hyposectomy 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 5 hemorheological measurement http://www.ebi.ac.uk/efo/EFO_0803374 GCST90255656 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Erythrocyte aggregation index 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 4 erythrocyte aggregation http://www.ebi.ac.uk/efo/EFO_0803375 GCST90255657 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Erythrocyte rigidity index 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 3 hemorheological measurement http://www.ebi.ac.uk/efo/EFO_0803374 GCST90255658 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Erythrocyte deformation index 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 2 erythrocyte deformability http://www.ebi.ac.uk/efo/EFO_0803376 GCST90255659 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Assigned viscosity 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 1 blood viscosity http://www.ebi.ac.uk/efo/EFO_0004301 GCST90255660 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Fibrinogen 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 4 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90255661 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Whole blood high cut reduction viscosity 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 5 blood viscosity http://www.ebi.ac.uk/efo/EFO_0004301 GCST90255662 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Whole blood high cut relative index 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 3 blood viscosity http://www.ebi.ac.uk/efo/EFO_0004301 GCST90255663 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Whole blood low cut reduction viscosity 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 6 blood viscosity http://www.ebi.ac.uk/efo/EFO_0004301 GCST90255664 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Plasma viscosity 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 6 blood viscosity http://www.ebi.ac.uk/efo/EFO_0004301 GCST90255665 Genome-wide genotyping array 2023-05-15 36654975 Sun Y 2022-07-05 Transfus Med Hemother www.ncbi.nlm.nih.gov/pubmed/36654975 Preliminary Study of Genome-Wide Association Identified Novel Susceptibility Genes for Hemorheological Indexes in a Chinese Population. Hematocrit 838 Han Chinese ancestry individuals NA NR [6423076] (imputed) 1 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90255666 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. aPTT in Platelet poor plasma by Coagulation assay 19,031 European ancestry individuals NA Illumina [6240610] (imputed) 0 prothrombin time measurement http://www.ebi.ac.uk/efo/EFO_0008390 GCST90012725 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Q ONSET from EKG 6,923 European ancestry individuals NA Illumina [6240610] (imputed) 0 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST90012726 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. QRS duration 6,920 European ancestry individuals NA Illumina [6240610] (imputed) 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90012727 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. QRS axis.horizontal plane Reference beat from EKG 6,798 European ancestry individuals NA Illumina [6240610] (imputed) 0 QRS duration http://www.ebi.ac.uk/efo/EFO_0005055 GCST90012728 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Triiodothyronine (T3) [Mass/volume] in Serum or Plasma 3,803 European ancestry individuals NA Illumina [6240610] (imputed) 0 triiodothyronine measurement http://www.ebi.ac.uk/efo/EFO_0008392 GCST90012729 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Mycobacterium tuberculosis stimulated gamma interferon release by CD4+ T-cells [Units/volume] corrected for background in Blood 1,948 European ancestry individuals NA Illumina [6240610] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90012730 Genome-wide genotyping array 2023-03-09 33441150 Dennis JK 2021-01-13 Genome Med www.ncbi.nlm.nih.gov/pubmed/33441150 Clinical laboratory test-wide association scan of polygenic scores identifies biomarkers of complex disease. Gamma interferon background [Units/volume] in Blood by Immunoassay 2,110 European ancestry individuals NA Illumina [6240610] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90012731 Genome-wide genotyping array 2023-03-21 35876483 Luo J 2022-07-25 Connect Tissue Res www.ncbi.nlm.nih.gov/pubmed/35876483 Genome-wide association study of handgrip strength in the Northern Chinese adult twins. Hand grip strength 135 Northern Chinese ancestry dizygotic twin pairs NA Illumina [7393353] (imputed) 30 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90258643 Genome-wide genotyping array 2023-07-18 37033223 Tan Y 2023-03-22 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37033223 Identification of shared genetic architecture between non-alcoholic fatty liver disease and type 2 diabetes: A genome-wide analysis. Non-alcoholic fatty liver disease or type 2 diabetes 1,483 European ancestry non-alcoholic fatty liver disease cases, 4,040 European ancestry type 2 diabetes cases, 131,516 European ancestry controls NA NR [NR] 74 non-alcoholic fatty liver disease, type 2 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0003095, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90272881 Genome-wide genotyping array 2023-03-24 36252120 Saad M 2022-10-12 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/36252120 Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing. Coronary heart disease 1,014 Greater Middle Eastern (Middle Eastern, North African or Persian) cases, 6,009 Greater Middle Eastern (Middle Eastern, North African or Persian) controls 163,854 European ancestry cases, 867,283 European ancestry controls, 79,166 European ancestry cases, 145,743 European ancestry controls, 79,166 South Asian ancestry cases, 145,743 South Asian ancestry controls, 25,892 Japanese ancestry cases, 142,336 Japanese ancestry controls NR [8278388] 21 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90258671 Genome-wide sequencing 2023-03-21 36244801 Wendt FR 2022-08-05 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36244801 Sex-Specific Genetic and Transcriptomic Liability to Neuroticism. Neuroticism 129,229 European ancestry men NA NR [NR] (imputed) 12 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90258646 Genome-wide genotyping array 2023-03-21 36244801 Wendt FR 2022-08-05 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36244801 Sex-Specific Genetic and Transcriptomic Liability to Neuroticism. Neuroticism 145,669 European ancestry women NA NR [NR] (imputed) 17 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90258647 Genome-wide genotyping array 2023-06-13 37248441 Adlam D 2023-05-29 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37248441 Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation. Spontaneous coronary artery dissection 1,917 European ancestry cases, 9,292 European ancestry controls NA Affymetrix, Illumina [6691677] (imputed) 17 spontaneous coronary artery dissection http://www.ebi.ac.uk/efo/EFO_0010820 GCST90245878 Genome-wide genotyping array, Genome-wide sequencing [OmniExpressExome|Human660W|Axiom UKBB|GSA|HumanHap550-610-660| CoreExome-24 UM_HUNT_Biobank] 2023-03-30 36944631 Khurshid S 2023-03-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36944631 Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass. Left ventricular mass indexed by body surface area 41,855 European ancestry individuals, 577 Asian or Pacific Islander individuals, 273 Black individuals, 198 Mixed ancestry individuals, 327 individuals NA NR [9851680] (imputed) 29 left ventricular mass index http://www.ebi.ac.uk/efo/EFO_0009290 GCST90244710 Genome-wide genotyping array 2023-03-30 36944631 Khurshid S 2023-03-21 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36944631 Clinical and genetic associations of deep learning-derived cardiac magnetic resonance-based left ventricular mass. Left ventricular mass 41,855 European ancestry individuals, 577 Asian or Pacific Islander individuals, 273 Black individuals, 198 Mixed ancestry individuals, 327 individuals NA NR [9851680] (imputed) 11 left ventricular mass http://www.ebi.ac.uk/efo/EFO_0009289 GCST90244711 Genome-wide genotyping array 2023-03-30 36376028 Henkel C 2022-11-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36376028 Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement. Surgical knee osteoarthritis 22,525 European ancestry cases, 638,618 European ancestry controls NA Affymetrix, Illumina [23151841] (imputed) 17 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90264170 Genome-wide genotyping array 2023-03-30 36376028 Henkel C 2022-11-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36376028 Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement. Non-surgical knee osteoarthritis 38,626 European ancestry cases, 625,232 European ancestry controls NA Affymetrix, Illumina [23151841] (imputed) 5 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90264171 Genome-wide genotyping array 2023-03-30 36376028 Henkel C 2022-11-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36376028 Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement. Surgical hip osteoarthritis 20,221 European ancestry cases, 626,610 European ancestry controls NA Affymetrix, Illumina [23151841] (imputed) 34 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90264172 Genome-wide genotyping array 2023-03-30 36376028 Henkel C 2022-11-14 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36376028 Genome-wide association meta-analysis of knee and hip osteoarthritis uncovers genetic differences between patients treated with joint replacement and patients without joint replacement. Non-surgical hip osteoarthritis 17,847 European ancestry cases, 672,115 European ancestry controls NA Affymetrix, Illumina [23151841] (imputed) 7 osteoarthritis, hip http://www.ebi.ac.uk/efo/EFO_1000786 GCST90264173 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Pharyngeal disease 33,157 Finnish ancestry cases, 199,208 Finnish ancestry controls NA NR [16355289] (imputed) 34 disorder of pharynx http://purl.obolibrary.org/obo/MONDO_0020592 GCST90269785 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Sinonasal disease 25,235 Finnish ancestry cases, 199,208 Finnish ancestry controls NA NR [16355289] (imputed) 21 nasal disorder http://purl.obolibrary.org/obo/MONDO_0002436 GCST90269786 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J35: Chronic diseases of tonsils and adenoids 29,135 Finnish ancestry cases, 199,208 Finnish ancestry controls 1,180 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 19 GCST90269775 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J37: Chronic laryngitis and laryngotracheitis 2,623 Finnish ancestry cases, 199,208 Finnish ancestry controls 951 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90269776 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J31: Chronic rhinitis, nasopharyngitis and pharyngitis 6,518 Finnish ancestry cases, 199,208 Finnish ancestry controls 13,694 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 0 upper respiratory tract disorder http://purl.obolibrary.org/obo/MONDO_0004867 GCST90269777 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J32: Chronic rhinosinusitis 10,435 Finnish ancestry cases, 199,208 Finnish ancestry controls 7,460 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 5 chronic rhinosinusitis http://www.ebi.ac.uk/efo/EFO_1000024 GCST90269778 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J33: nasal polyps 3,919 Finnish ancestry cases, 199,208 Finnish ancestry controls 4,401 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 12 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90269779 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J34.2: Deviated nasal septum 7,716 Finnish ancestry cases, 199,208 Finnish ancestry controls 4,840 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 3 nasal disorder http://purl.obolibrary.org/obo/MONDO_0002436 GCST90269780 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J36: Peritonsillar abscess 4,863 Finnish ancestry cases, 199,208 Finnish ancestry controls 633 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 5 peritonsillar abscess http://www.ebi.ac.uk/efo/EFO_0007429 GCST90269781 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 J30: Vasomotor and allergic rhinitis 8,975 Finnish ancestry cases, 199,208 Finnish ancestry controls 16,751 European ancestry cases, 298,846 European ancestry controls NR [16355289] (imputed) 5 rhinitis http://www.ebi.ac.uk/efo/EFO_0008521 GCST90269782 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Inflammatory or infectious upper respiratory disease 61,197 Finnish ancestry cases, 199,208 Finnish ancestry controls NA NR [16355289] (imputed) 20 upper respiratory tract disorder http://purl.obolibrary.org/obo/MONDO_0004867 GCST90269783 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Chronic inflammatory sinonasal disease 19,901 Finnish ancestry cases, 199,208 Finnish ancestry controls NA NR [16355289] (imputed) 21 nasal disorder http://purl.obolibrary.org/obo/MONDO_0002436 GCST90269784 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 K04: Diseases of pulp and periapical tissues 48,687 Finnish ancestry cases, 211,718 Finnish ancestry controls NA NR [16355289] (imputed) 3 dental pulp disease http://www.ebi.ac.uk/efo/EFO_0009540 GCST90269794 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Vasomotor rhinitis or allergic rhinitis (MTAG) at least 8,975 Finnish ancestry cases, 199,208 Finnish ancestry controls (MTAG boosted by additional inflammatory and infectious upper respiratory disease samples) NA NR [6868381] (imputed) 8 rhinitis http://www.ebi.ac.uk/efo/EFO_0008521 GCST90269787 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Chronic rhinitis or nasopharyngitis or pharyngitis (MTAG) at least 6,518 Finnish ancestry cases, 199,208 Finnish ancestry controls (MTAG boosted by additional inflammatory and infectious upper respiratory disease samples) NA NR [6868381] (imputed) 5 upper respiratory tract disorder http://purl.obolibrary.org/obo/MONDO_0004867 GCST90269788 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Chronic rhinosinusitis (MTAG) at least 10,435 Finnish ancestry cases, 199,208 Finnish ancestry controls (MTAG boosted by additional inflammatory and infectious upper respiratory disease samples) NA NR [6868381] (imputed) 9 chronic rhinosinusitis http://www.ebi.ac.uk/efo/EFO_1000024 GCST90269789 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Nasal polyposis (MTAG) at least 3,919 Finnish ancestry cases, 199,208 Finnish ancestry controls (MTAG boosted by additional inflammatory and infectious upper respiratory disease samples) NA NR [6868381] (imputed) 13 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90269790 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Nasal septal deviation (MTAG) at least 7,716 Finnish ancestry cases, 199,208 Finnish ancestry controls (MTAG boosted by additional inflammatory and infectious upper respiratory disease samples) NA NR [6868381] (imputed) 8 nasal disorder http://purl.obolibrary.org/obo/MONDO_0002436 GCST90269791 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Chronic diseases of tonsils or adenoids (MTAG) at least 29,135 Finnish ancestry cases, 199,208 Finnish ancestry controls (MTAG boosted by additional inflammatory and infectious upper respiratory disease samples) NA NR [6868381] (imputed) 18 GCST90269792 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. Peritonsillar abscess (MTAG) at least 4,863 Finnish ancestry cases, 199,208 Finnish ancestry controls (MTAG boosted by additional inflammatory and infectious upper respiratory disease samples) NA NR [6868381] (imputed) 11 peritonsillar abscess http://www.ebi.ac.uk/efo/EFO_0007429 GCST90269793 Genome-wide genotyping array 2023-06-26 36653354 Saarentaus EC 2023-01-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36653354 Inflammatory and infectious upper respiratory diseases associate with 41 genomic loci and type 2 inflammation. ICD10 K05.30-31: Chronic periodontitis 14,631 Finnish ancestry cases, 245,774 Finnish ancestry controls NA NR [16355289] (imputed) 1 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90269795 Genome-wide genotyping array 2023-04-19 36929174 Koel M 2023-03-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36929174 GWAS meta-analyses clarify genetics of cervical phenotypes and inform risk stratification for cervical cancer. Cervical ectropion 10,162 European ancestry cases, 151,347 European ancestry controls NA Illumina [11043344] (imputed) 1 Cervical ectropion http://purl.obolibrary.org/obo/HP_0030158 GCST90246355 Genome-wide genotyping array 2023-04-19 36929174 Koel M 2023-03-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36929174 GWAS meta-analyses clarify genetics of cervical phenotypes and inform risk stratification for cervical cancer. Cervicitis 19,285 European ancestry cases, 185,708 European ancestry controls NA Illumina [11043696] (imputed) 1 Cervicitis http://purl.obolibrary.org/obo/HP_0030160 GCST90246356 Genome-wide genotyping array 2023-04-19 36929174 Koel M 2023-03-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36929174 GWAS meta-analyses clarify genetics of cervical phenotypes and inform risk stratification for cervical cancer. Cervical dysplasia 14,694 European ancestry cases, 150,563 European ancestry controls NA Illumina [11043396] (imputed) 6 dysplasia of cervix http://www.ebi.ac.uk/efo/EFO_1000910 GCST90246357 Genome-wide genotyping array 2023-04-19 36929174 Koel M 2023-03-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36929174 GWAS meta-analyses clarify genetics of cervical phenotypes and inform risk stratification for cervical cancer. Cervical cancer 8,624 European ancestry cases, 400,573 European ancestry controls NA Illumina [8805880] (imputed) 5 cervical cancer http://purl.obolibrary.org/obo/MONDO_0002974 GCST90246358 Genome-wide genotyping array 2023-04-19 36929174 Koel M 2023-03-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36929174 GWAS meta-analyses clarify genetics of cervical phenotypes and inform risk stratification for cervical cancer. Cervical cancer 8,624 European ancestry cases, 400,573 European ancestry controls, 605 East Asian ancestry cases, 89,731 East Asian ancestry controls NA Illumina [5143473] (imputed) 6 cervical cancer http://purl.obolibrary.org/obo/MONDO_0002974 GCST90246359 Genome-wide genotyping array 2023-04-19 36929174 Koel M 2023-03-16 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36929174 GWAS meta-analyses clarify genetics of cervical phenotypes and inform risk stratification for cervical cancer. Cervical dysplasia or cervical cancer (MTAG) 14,694 European ancestry dysplasia cases, 8,624 European ancestry cervical cancer cases, 551,136 European ancestry controls NA Illumina [NR] (imputed) 1 dysplasia of cervix, cervical cancer http://www.ebi.ac.uk/efo/EFO_1000910, http://purl.obolibrary.org/obo/MONDO_0002974 GCST90266933 Genome-wide genotyping array 2023-05-11 36939796 Meng W 2022-11-18 Phenomics www.ncbi.nlm.nih.gov/pubmed/36939796 A Meta-Analysis of the Genome-Wide Association Studies on Two Genetically Correlated Phenotypes Suggests Four New Risk Loci for Headaches. Headache or migraine 397,385 European ancestry individuals NA NR [8500802] (imputed) 113 migraine disorder, Headache http://purl.obolibrary.org/obo/MONDO_0005277, http://purl.obolibrary.org/obo/HP_0002315 GCST90267554 Genome-wide genotyping array 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (gene-based - predicted loss of function) 156,259 European ancestry individuals, 26,759 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256837 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (kernel-based - missense) 156,259 European ancestry individuals, 26,759 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256838 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (gene-based - collapsed missense) 156,259 European ancestry individuals, 26,759 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256839 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (kernel-based - splice) 156,259 European ancestry individuals, 26,759 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256840 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (gene-based - collapsed splice) 156,259 European ancestry individuals, 26,759 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256841 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (gene-based - predicted loss of function) 142,409 European ancestry individuals, 24,440 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256842 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (kernel-based - missense) 142,409 European ancestry individuals, 24,440 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256843 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (gene-based - collapsed missense) 142,409 European ancestry individuals, 24,440 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256844 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (kernel-based - splice) 142,409 European ancestry individuals, 24,440 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256845 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (gene-based - collapsed splice) 142,409 European ancestry individuals, 24,440 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256846 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (gene-based - predicted loss of function) 25,052 European ancestry individuals, 5,357 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256847 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (kernel-based - missense) 25,052 European ancestry individuals, 5,357 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256848 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (gene-based - collapsed missense) 25,052 European ancestry individuals, 5,357 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256849 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (kernel-based - splice) 25,052 European ancestry individuals, 5,357 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256850 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (gene-based - collapsed splice) 25,052 European ancestry individuals, 5,357 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256851 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (gene-based - predicted loss of function) 156,246 European ancestry individuals, 26,755 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256852 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (kernel-based - missense) 156,246 European ancestry individuals, 26,755 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256853 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (gene-based - collapsed missense) 156,246 European ancestry individuals, 26,755 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256854 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (kernel-based - splice) 156,246 European ancestry individuals, 26,755 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256855 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (gene-based - collapsed splice) 156,246 European ancestry individuals, 26,755 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256856 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (gene-based - predicted loss of function) 156,322 European ancestry individuals, 26,761 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256857 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (kernel-based - missense) 156,322 European ancestry individuals, 26,761 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256858 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (gene-based - collapsed missense) 156,322 European ancestry individuals, 26,761 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256859 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (kernel-based - splice) 156,322 European ancestry individuals, 26,761 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256860 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (gene-based - collapsed splice) 156,322 European ancestry individuals, 26,761 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256861 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (gene-based - predicted loss of function) 156,246 European ancestry individuals NA NR [12793493] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256912 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (kernel-based - missense) 156,246 European ancestry individuals NA NR [12793493] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256913 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (gene-based - collapsed missense) 156,246 European ancestry individuals NA NR [12793493] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256914 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (kernel-based - splice) 156,246 European ancestry individuals NA NR [12793493] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256915 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Creatinine levels (gene-based - collapsed splice) 156,246 European ancestry individuals NA NR [12793493] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90256916 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (gene-based - predicted loss of function) 156,259 European ancestry individuals NA NR [12793493] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256917 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (kernel-based - missense) 156,259 European ancestry individuals NA NR [12793493] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256918 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (gene-based - collapsed missense) 156,259 European ancestry individuals NA NR [12793493] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256919 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (kernel-based - splice) 156,259 European ancestry individuals NA NR [12793493] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256920 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Gamma glutamyltransferase levels (gene-based - collapsed splice) 156,259 European ancestry individuals NA NR [12793493] 0 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90256921 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (gene-based - predicted loss of function) 156,289 European ancestry individuals NA NR [12793493] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256922 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (kernel-based - missense) 156,289 European ancestry individuals NA NR [12793493] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256923 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (gene-based - collapsed missense) 156,289 European ancestry individuals NA NR [12793493] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256924 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (kernel-based - splice) 156,289 European ancestry individuals NA NR [12793493] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256925 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (gene-based - collapsed splice) 156,289 European ancestry individuals NA NR [12793493] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256926 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (gene-based - predicted loss of function) 155,704 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256927 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (kernel-based - missense) 155,704 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256928 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (gene-based - collapsed missense) 155,704 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256929 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (kernel-based - splice) 155,704 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256930 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (gene-based - collapsed splice) 155,704 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256931 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (gene-based - predicted loss of function) 155,984 European ancestry individuals NA NR [12793493] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256932 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (kernel-based - missense) 155,984 European ancestry individuals NA NR [12793493] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256933 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (gene-based - collapsed missense) 155,984 European ancestry individuals NA NR [12793493] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256934 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (kernel-based - splice) 155,984 European ancestry individuals NA NR [12793493] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256935 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (gene-based - collapsed splice) 155,984 European ancestry individuals NA NR [12793493] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256936 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (gene-based - predicted loss of function) 143,717 European ancestry individuals NA NR [12793493] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256862 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (kernel-based - missense) 143,717 European ancestry individuals NA NR [12793493] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256863 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (gene-based - collapsed missense) 143,717 European ancestry individuals NA NR [12793493] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256864 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (kernel-based - splice) 143,717 European ancestry individuals NA NR [12793493] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256865 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (gene-based - collapsed splice) 143,717 European ancestry individuals NA NR [12793493] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256866 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (gene-based - predicted loss of function) 143,606 European ancestry individuals NA NR [12793493] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256867 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (kernel-based - missense) 143,606 European ancestry individuals NA NR [12793493] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256868 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (gene-based - collapsed missense) 143,606 European ancestry individuals NA NR [12793493] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256869 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (kernel-based - splice) 143,606 European ancestry individuals NA NR [12793493] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256870 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (gene-based - collapsed splice) 143,606 European ancestry individuals NA NR [12793493] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256871 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (gene-based - predicted loss of function) 156,501 European ancestry individuals NA NR [12793493] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256872 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (kernel-based - missense) 156,501 European ancestry individuals NA NR [12793493] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256873 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (gene-based - collapsed missense) 156,501 European ancestry individuals NA NR [12793493] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256874 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (kernel-based - splice) 156,501 European ancestry individuals NA NR [12793493] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256875 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (gene-based - collapsed splice) 156,501 European ancestry individuals NA NR [12793493] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256876 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (gene-based - predicted loss of function) 155,502 European ancestry individuals NA NR [12793493] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256877 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (kernel-based - missense) 155,502 European ancestry individuals NA NR [12793493] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256878 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (gene-based - collapsed missense) 155,502 European ancestry individuals NA NR [12793493] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256879 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (kernel-based - splice) 155,502 European ancestry individuals NA NR [12793493] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256880 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (gene-based - collapsed splice) 155,502 European ancestry individuals NA NR [12793493] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256881 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (gene-based - predicted loss of function) 155,580 European ancestry individuals NA NR [12793493] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256882 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (kernel-based - missense) 155,580 European ancestry individuals NA NR [12793493] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256883 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (gene-based - collapsed missense) 155,580 European ancestry individuals NA NR [12793493] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256884 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (kernel-based - splice) 155,580 European ancestry individuals NA NR [12793493] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256885 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (gene-based - collapsed splice) 155,580 European ancestry individuals NA NR [12793493] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256886 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (gene-based - predicted loss of function) 143,716 European ancestry individuals, 24,664 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90256787 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (kernel-based - missense) 143,716 European ancestry individuals, 24,664 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90256788 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (gene-based - collapsed missense) 143,716 European ancestry individuals, 24,664 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90256789 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (kernel-based - splice) 143,716 European ancestry individuals, 24,664 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90256790 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (gene-based - collapsed splice) 143,716 European ancestry individuals, 24,664 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90256791 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (gene-based - predicted loss of function) 156,329 European ancestry individuals, 26,769 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256792 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (kernel-based - missense) 156,329 European ancestry individuals, 26,769 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256793 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (gene-based - collapsed missense) 156,329 European ancestry individuals, 26,769 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256794 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (kernel-based - splice) 156,329 European ancestry individuals, 26,769 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256795 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (gene-based - collapsed splice) 156,329 European ancestry individuals, 26,769 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256796 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (gene-based - predicted loss of function) 156,167 European ancestry individuals, 26,733 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256797 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (kernel-based - missense) 156,167 European ancestry individuals, 26,733 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256798 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (gene-based - collapsed missense) 156,167 European ancestry individuals, 26,733 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256799 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (kernel-based - splice) 156,167 European ancestry individuals, 26,733 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256800 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (gene-based - collapsed splice) 156,167 European ancestry individuals, 26,733 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256801 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (gene-based - predicted loss of function) 143,612 European ancestry individuals, 24,647 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256802 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (kernel-based - missense) 143,612 European ancestry individuals, 24,647 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256803 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (gene-based - collapsed missense) 143,612 European ancestry individuals, 24,647 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256804 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (kernel-based - splice) 143,612 European ancestry individuals, 24,647 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256805 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (gene-based - collapsed splice) 143,612 European ancestry individuals, 24,647 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256806 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (gene-based - predicted loss of function) 124,389 European ancestry individuals, 22,145 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256807 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (kernel-based - missense) 124,389 European ancestry individuals, 22,145 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256808 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (gene-based - collapsed missense) 124,389 European ancestry individuals, 22,145 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256809 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (kernel-based - splice) 124,389 European ancestry individuals, 22,145 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256810 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (gene-based - collapsed splice) 124,389 European ancestry individuals, 22,145 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256811 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (gene-based - predicted loss of function) 142,855 European ancestry individuals NA NR [12793493] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256887 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (kernel-based - missense) 142,855 European ancestry individuals NA NR [12793493] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256888 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (gene-based - collapsed missense) 142,855 European ancestry individuals NA NR [12793493] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256889 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (kernel-based - splice) 142,855 European ancestry individuals NA NR [12793493] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256890 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (gene-based - collapsed splice) 142,855 European ancestry individuals NA NR [12793493] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256891 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (gene-based - predicted loss of function) 156,201 European ancestry individuals NA NR [12793493] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256892 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (kernel-based - missense) 156,201 European ancestry individuals NA NR [12793493] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256893 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (gene-based - collapsed missense) 156,201 European ancestry individuals NA NR [12793493] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256894 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (kernel-based - splice) 156,201 European ancestry individuals NA NR [12793493] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256895 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (gene-based - collapsed splice) 156,201 European ancestry individuals NA NR [12793493] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256896 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (gene-based - predicted loss of function) 143,798 European ancestry individuals NA NR [12793493] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256897 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (kernel-based - missense) 143,798 European ancestry individuals NA NR [12793493] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256898 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (gene-based - collapsed missense) 143,798 European ancestry individuals NA NR [12793493] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256899 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (kernel-based - splice) 143,798 European ancestry individuals NA NR [12793493] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256900 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (gene-based - collapsed splice) 143,798 European ancestry individuals NA NR [12793493] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256901 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (gene-based - predicted loss of function) 132,847 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256902 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (kernel-based - missense) 132,847 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256903 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (gene-based - collapsed missense) 132,847 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256904 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (kernel-based - splice) 132,847 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256905 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (gene-based - collapsed splice) 132,847 European ancestry individuals NA NR [12793493] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256906 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (gene-based - predicted loss of function) 143,612 European ancestry individuals NA NR [12793493] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256907 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (kernel-based - missense) 143,612 European ancestry individuals NA NR [12793493] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256908 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (gene-based - collapsed missense) 143,612 European ancestry individuals NA NR [12793493] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256909 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (kernel-based - splice) 143,612 European ancestry individuals NA NR [12793493] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256910 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total protein levels (gene-based - collapsed splice) 143,612 European ancestry individuals NA NR [12793493] 0 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90256911 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (kernel-based - missense) 141,367 European ancestry individuals NA NR [12793493] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256938 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (gene-based - collapsed missense) 141,367 European ancestry individuals NA NR [12793493] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256939 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (kernel-based - splice) 141,367 European ancestry individuals NA NR [12793493] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256940 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (gene-based - collapsed splice) 141,367 European ancestry individuals NA NR [12793493] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256941 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (gene-based - predicted loss of function) 149,538 European ancestry individuals NA NR [12793493] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256942 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (kernel-based - missense) 149,538 European ancestry individuals NA NR [12793493] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256943 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (gene-based - collapsed missense) 149,538 European ancestry individuals NA NR [12793493] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256944 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (kernel-based - splice) 149,538 European ancestry individuals NA NR [12793493] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256945 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (gene-based - collapsed splice) 149,538 European ancestry individuals NA NR [12793493] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256946 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (gene-based - predicted loss of function) 156,340 European ancestry individuals NA NR [12793493] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256947 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (kernel-based - missense) 156,340 European ancestry individuals NA NR [12793493] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256948 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (gene-based - collapsed missense) 156,340 European ancestry individuals NA NR [12793493] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256949 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (kernel-based - splice) 156,340 European ancestry individuals NA NR [12793493] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256950 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (gene-based - collapsed splice) 156,340 European ancestry individuals NA NR [12793493] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256951 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (gene-based - predicted loss of function) 142,409 European ancestry individuals NA NR [12793493] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256952 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (kernel-based - missense) 142,409 European ancestry individuals NA NR [12793493] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256953 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (gene-based - collapsed missense) 142,409 European ancestry individuals NA NR [12793493] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256954 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (kernel-based - splice) 142,409 European ancestry individuals NA NR [12793493] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256955 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Sex hormone-binding globulin levels (gene-based - collapsed splice) 142,409 European ancestry individuals NA NR [12793493] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90256956 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (gene-based - predicted loss of function) 155,791 European ancestry individuals NA NR [12793493] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256957 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (kernel-based - missense) 155,791 European ancestry individuals NA NR [12793493] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256958 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (gene-based - collapsed missense) 155,791 European ancestry individuals NA NR [12793493] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256959 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (kernel-based - splice) 155,791 European ancestry individuals NA NR [12793493] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256960 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (gene-based - collapsed splice) 155,791 European ancestry individuals NA NR [12793493] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256961 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (gene-based - collapsed splice) 156,069 European ancestry individuals, 26,714 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256821 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (gene-based - predicted loss of function) 149,538 European ancestry individuals, 25,282 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256822 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (kernel-based - missense) 149,538 European ancestry individuals, 25,282 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256823 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (gene-based - collapsed missense) 149,538 European ancestry individuals, 25,282 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256824 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (kernel-based - splice) 149,538 European ancestry individuals, 25,282 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256825 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Vitamin D levels (gene-based - collapsed splice) 149,538 European ancestry individuals, 25,282 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90256826 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (gene-based - predicted loss of function) 155,580 European ancestry individuals, 26,588 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256827 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (kernel-based - missense) 155,580 European ancestry individuals, 26,588 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256828 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (gene-based - collapsed missense) 155,580 European ancestry individuals, 26,588 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256829 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (kernel-based - splice) 155,580 European ancestry individuals, 26,588 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256830 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein B levels (gene-based - collapsed splice) 155,580 European ancestry individuals, 26,588 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90256831 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (gene-based - predicted loss of function) 156,223 European ancestry individuals, 26,751 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90256832 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (kernel-based - missense) 156,223 European ancestry individuals, 26,751 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90256833 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (gene-based - collapsed missense) 156,223 European ancestry individuals, 26,751 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90256834 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (kernel-based - splice) 156,223 European ancestry individuals, 26,751 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90256835 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (gene-based - collapsed splice) 156,223 European ancestry individuals, 26,751 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90256836 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (gene-based - predicted loss of function) 156,501 European ancestry individuals, 26,350 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256812 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (kernel-based - missense) 156,501 European ancestry individuals, 26,350 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256813 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (gene-based - collapsed missense) 156,501 European ancestry individuals, 26,350 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256814 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (kernel-based - splice) 156,501 European ancestry individuals, 26,350 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256815 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glycated hemoglobin (HbA1c) levels (gene-based - collapsed splice) 156,501 European ancestry individuals, 26,350 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90256816 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (gene-based - predicted loss of function) 156,069 European ancestry individuals, 26,714 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256817 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (kernel-based - missense) 156,069 European ancestry individuals, 26,714 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256818 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (gene-based - collapsed missense) 156,069 European ancestry individuals, 26,714 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256819 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (kernel-based - splice) 156,069 European ancestry individuals, 26,714 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256820 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (gene-based - predicted loss of function) 141,367 European ancestry individuals NA NR [12793493] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256937 Exome-wide sequencing 2023-03-31 36444934 Pan Y 2022-11-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36444934 Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease. Diabetic kidney disease 296 European ancestry cases, 1,660 European ancestry controls, 297 African or African American cases, 406 African or African American controls 154 Hispanic/Latino or Asian ancestry cases, 888 Hispanic/Latino or Asian ancestry controls, 265 African or African American cases, 1,738 African or African American controls, 182 European ancestry cases, 4,876 European ancestry controls Illumina [NR] 2 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90266982 Exome-wide sequencing 2023-03-31 36444934 Pan Y 2022-11-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36444934 Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease. Diabetic kidney disease 297 African or African American cases, 406 African or African American controls 265 African or African American cases, 1,738 African or African American controls Illumina [NR] 0 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90266983 Exome-wide sequencing 2023-03-31 36444934 Pan Y 2022-11-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36444934 Whole-Exome Sequencing Study Identifies Four Novel Gene Loci Associated with Diabetic Kidney Disease. Diabetic kidney disease 296 European ancestry cases, 1,660 European ancestry controls 182 European ancestry cases, 4,876 European ancestry controls Illumina [NR] 2 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90266984 Exome-wide sequencing 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. Age at adiposity rebound x sex interaction 904 Admixed Chileans with European and Native American ancestry individuals NA Illumina [607621] 10 sex interaction measurement, longitudinal BMI measurement, age at assessment http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0005937, http://www.ebi.ac.uk/efo/EFO_0008007 GCST90132242 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at adiposity rebound x sex interaction 904 Admixed Chileans with European and Native American ancestry individuals NA Illumina [607607] 8 sex interaction measurement, longitudinal BMI measurement http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0005937 GCST90132243 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 0.5 - 1.5 years old interval 718 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609122] 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132244 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 1.5 -2.5 years old interval 684 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609122] 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132245 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 2.5 - 3.5 years old interval 504 Admixed Chileans with European and Native American ancestry individuals NA Illumina [608972] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132246 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 3.5 - 4.5 years old interval 642 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609113] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132247 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 4.5 - 5.5 years old interval 788 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132248 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 5.5 -6.5 years old interval 483 Admixed Chileans with European and Native American ancestry individuals NA Illumina [608907] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132249 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 6.5 -7.5 years old interval 803 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132250 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 7.5 - 8.5 years old interval 829 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132251 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 8.5 - 9.5 years old interval 828 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132252 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 9.5 - 10.5 years old interval 841 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132253 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 10.5 - 11.5 years old interval 795 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132254 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 11.5 -12.5 years old interval 667 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609121] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132255 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 12.5 - 13.5 years old interval 748 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132256 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 13.5 - 14.5 years old interval 782 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132257 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 14.5 - 15.5 years old interval 780 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609123] 1 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132258 Genome-wide genotyping array 2023-03-21 36844456 Vicuna L 2023-01-31 iScience www.ncbi.nlm.nih.gov/pubmed/36844456 New insights from GWAS on BMI-related growth traits in a longitudinal cohort of admixed children with Native American and European ancestry. BMI at 15.5 - 16.5 years old interval 587 Admixed Chileans with European and Native American ancestry individuals NA Illumina [609103] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90132259 Genome-wide genotyping array 2023-08-09 37110199 Kim HR 2023-04-10 Metabolites www.ncbi.nlm.nih.gov/pubmed/37110199 Identification of Genetic Markers Linked to The Activity of Indoleamine 2,3-Dioxygenase and Kidney Function. Indoleamine 2,3-dioxygenase activity 2,579 Korean ancestry individuals NA NR [6461358] (imputed) 0 indoleamine 2,3-dioxygenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0801695 GCST90277417 Genome-wide genotyping array 2023-08-09 37110199 Kim HR 2023-04-10 Metabolites www.ncbi.nlm.nih.gov/pubmed/37110199 Identification of Genetic Markers Linked to The Activity of Indoleamine 2,3-Dioxygenase and Kidney Function. Chronic kidney disease 264 Korean ancestry cases, 1,550 Korean ancestry controls NA NR [6461358] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90277418 Genome-wide genotyping array 2023-11-08 35156446 Shade LM 2022-02-14 J Cereb Blood Flow Metab www.ncbi.nlm.nih.gov/pubmed/35156446 Genome-wide association study of brain arteriolosclerosis. Brain arteriolosclerosis 2,184 European ancestry cases, 2,944 European ancestry controls NA NR [4470488] (imputed) 9 cerebral atherosclerosis http://www.ebi.ac.uk/efo/EFO_1000860 GCST90134619 Genome-wide genotyping array 2023-03-30 36378351 Williams CM 2022-11-15 Behav Genet www.ncbi.nlm.nih.gov/pubmed/36378351 A General Cognitive Ability Factor for the UK Biobank. Intelligence 223,731 British ancestry individuals NA Affymetrix [5319661] (imputed) 352 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST90264174 Genome-wide genotyping array 2023-05-11 36766075 Park S 2023-01-26 Foods www.ncbi.nlm.nih.gov/pubmed/36766075 A Causal and Inverse Relationship between Plant-Based Diet Intake and in a Two-Sample Mendelian Randomization Study. Highly plant-based diet 11,740 Korean ancestry cases, 46,961 Korean ancestry controls NA Affymetrix [K-Chip] (imputed) 10 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90269773 Genome-wide genotyping array 2022-12-12 36376304 Koskeridis F 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376304 Pleiotropic genetic architecture and novel loci for C-reactive protein levels. C-reactive protein levels (MTAG) 575,531 European ancestry individuals NA NR [6206408] (imputed) 797 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90179146 Genome-wide genotyping array 2022-12-12 36376304 Koskeridis F 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376304 Pleiotropic genetic architecture and novel loci for C-reactive protein levels. High-density lipoprotein levels (MTAG) 361,194 European ancestry individuals NA NR [6206408] (imputed) 549 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90179147 Genome-wide genotyping array 2022-12-12 36376304 Koskeridis F 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376304 Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Low-density lipoprotein levels (MTAG) 361,194 European ancestry individuals NA NR [6206408] (imputed) 527 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90179148 Genome-wide genotyping array 2022-12-12 36376304 Koskeridis F 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376304 Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Triglyceride levels (MTAG) 361,194 European ancestry individuals NA NR [6206408] (imputed) 534 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90179149 Genome-wide genotyping array 2022-12-12 36376304 Koskeridis F 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376304 Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Body mass index (MTAG) 694,649 European ancestry individuals NA NR [6206408] (imputed) 1552 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90179150 Genome-wide genotyping array 2022-12-12 36376304 Koskeridis F 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376304 Pleiotropic genetic architecture and novel loci for C-reactive protein levels. Cigarettes smoked per day (MTAG) 337,334 European ancestry individuals NA NR [6206408] (imputed) 108 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90179151 Genome-wide genotyping array 2023-04-21 36581688 Bhatt IS 2022-12-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36581688 A genome-wide association study of tinnitus reveals shared genetic links to neuropsychiatric disorders. Tinnitus 132,438 European ancestry individuals NA Affymetrix [8357671] (imputed) 94 Tinnitus http://purl.obolibrary.org/obo/HP_0000360 GCST90267564 Genome-wide genotyping array 2023-04-21 36581688 Bhatt IS 2022-12-29 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36581688 A genome-wide association study of tinnitus reveals shared genetic links to neuropsychiatric disorders. Tinnitus-related distress 132,164 European ancestry individuals NA Affymetrix [8357671] (imputed) 74 Tinnitus, wellbeing measurement http://purl.obolibrary.org/obo/HP_0000360, http://www.ebi.ac.uk/efo/EFO_0007869 GCST90255650 Genome-wide genotyping array 2023-03-22 35925860 Mathebula EM 2022-08-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35925860 A genome-wide association study for rheumatoid arthritis replicates previous HLA and non-HLA associations in a cohort from South Africa. Rheumatoid arthritis 531 South-Eastern Bantu-Speaking South African ancestry cases, 26,353 South-Eastern Bantu-Speaking South African ancestry controls NA Illumina [7908047] (imputed) 17 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90258644 Genome-wide genotyping array 2023-03-22 35925860 Mathebula EM 2022-08-04 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35925860 A genome-wide association study for rheumatoid arthritis replicates previous HLA and non-HLA associations in a cohort from South Africa. Rheumatoid arthritis 531 South-Eastern Bantu-Speaking South African ancestry cases, 26,353 South-Eastern Bantu-Speaking South African ancestry controls, 916 African American cases, 1,370 African American controls NA Illumina [7908047] (imputed) 8 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90258645 Genome-wide genotyping array 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (gene-based - predicted loss of function) 141,367 European ancestry individuals, 24,170 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256712 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (kernel-based - missense) 142,855 European ancestry individuals, 24,520 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256738 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (gene-based - collapsed missense) 141,367 European ancestry individuals, 24,170 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256714 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (kernel-based - splice) 141,367 European ancestry individuals, 24,170 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256715 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (kernel-based - splice) 142,855 European ancestry individuals, 24,520 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256740 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (gene-based - predicted loss of function) 156,340 European ancestry individuals, 26,765 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256717 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (kernel-based - missense) 156,340 European ancestry individuals, 26,765 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256718 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (gene-based - collapsed missense) 156,340 European ancestry individuals, 26,765 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256719 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (kernel-based - splice) 156,340 European ancestry individuals, 26,765 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256720 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alkaline phosphatase levels (gene-based - collapsed splice) 156,340 European ancestry individuals, 26,765 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90256721 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (gene-based - predicted loss of function) 156,289 European ancestry individuals, 26,748 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256722 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (gene-based - predicted loss of function) 143,717 European ancestry individuals, 24,654 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256747 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (gene-based - collapsed missense) 156,289 European ancestry individuals, 26,748 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256724 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (gene-based - collapsed missense) 143,717 European ancestry individuals, 24,654 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256749 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (kernel-based - splice) 143,717 European ancestry individuals, 24,654 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256750 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (gene-based - predicted loss of function) 155,704 European ancestry individuals, 26,653 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256727 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (gene-based - predicted loss of function) 132,847 European ancestry individuals, 22,433 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256752 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (gene-based - collapsed missense) 155,704 European ancestry individuals, 26,653 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256729 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (gene-based - collapsed missense) 132,847 European ancestry individuals, 22,433 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256754 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (gene-based - collapsed splice) 155,704 European ancestry individuals, 26,653 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256731 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (gene-based - collapsed splice) 132,847 European ancestry individuals, 22,433 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256756 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (gene-based - predicted loss of function) 155,984 European ancestry individuals, 26,697 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256757 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (gene-based - collapsed missense) 155,502 European ancestry individuals, 26,617 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256734 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (gene-based - collapsed missense) 155,984 European ancestry individuals, 26,697 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256759 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (gene-based - collapsed splice) 155,502 European ancestry individuals, 26,617 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256736 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (gene-based - collapsed splice) 155,984 European ancestry individuals, 26,697 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256761 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (gene-based - predicted loss of function) 142,855 European ancestry individuals, 24,520 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256737 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (kernel-based - missense) 141,367 European ancestry individuals, 24,170 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256713 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (gene-based - collapsed missense) 142,855 European ancestry individuals, 24,520 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256739 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Testosterone levels (gene-based - collapsed splice) 141,367 European ancestry individuals, 24,170 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90256716 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Apolipoprotein A levels (gene-based - collapsed splice) 142,855 European ancestry individuals, 24,520 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90256741 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (gene-based - predicted loss of function) 143,798 European ancestry individuals, 24,669 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256742 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (kernel-based - missense) 143,798 European ancestry individuals, 24,669 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256743 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (gene-based - collapsed missense) 143,798 European ancestry individuals, 24,669 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256744 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (kernel-based - splice) 143,798 European ancestry individuals, 24,669 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256745 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Albumin levels (gene-based - collapsed splice) 143,798 European ancestry individuals, 24,669 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90256746 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (kernel-based - missense) 156,289 European ancestry individuals, 26,748 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256723 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (kernel-based - missense) 143,717 European ancestry individuals, 24,654 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256748 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (kernel-based - splice) 156,289 European ancestry individuals, 26,748 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256725 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Alanine aminotransferase levels (gene-based - collapsed splice) 156,289 European ancestry individuals, 26,748 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90256726 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. High density lipoprotein cholesterol levels (gene-based - collapsed splice) 143,717 European ancestry individuals, 24,654 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90256751 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (kernel-based - missense) 155,704 European ancestry individuals, 26,653 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256728 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (kernel-based - missense) 132,847 European ancestry individuals, 22,433 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256753 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Total bilirubin levels (kernel-based - splice) 155,704 European ancestry individuals, 26,653 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256730 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct bilirubin levels (kernel-based - splice) 132,847 European ancestry individuals, 22,433 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90256755 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (gene-based - predicted loss of function) 155,502 European ancestry individuals, 26,617 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256732 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (kernel-based - missense) 155,502 European ancestry individuals, 26,617 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256733 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (kernel-based - missense) 155,984 European ancestry individuals, 26,697 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256758 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Insulin-like growth factor 1 levels (kernel-based - splice) 155,502 European ancestry individuals, 26,617 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90256735 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. C-reactive protein levels (kernel-based - splice) 155,984 European ancestry individuals, 26,697 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90256760 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (gene-based - predicted loss of function) 155,791 European ancestry individuals, 26,665 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256762 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (kernel-based - missense) 155,791 European ancestry individuals, 26,665 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256763 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (gene-based - collapsed missense) 155,791 European ancestry individuals, 26,665 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256764 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (kernel-based - splice) 155,791 European ancestry individuals, 26,665 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256765 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Aspartate aminotransferase levels (gene-based - collapsed splice) 155,791 European ancestry individuals, 26,665 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90256766 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (gene-based - predicted loss of function) 143,606 European ancestry individuals, 24,638 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256767 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (kernel-based - missense) 143,606 European ancestry individuals, 24,638 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256768 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (gene-based - collapsed missense) 143,606 European ancestry individuals, 24,638 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256769 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (kernel-based - splice) 143,606 European ancestry individuals, 24,638 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256770 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Glucose levels (gene-based - collapsed splice) 143,606 European ancestry individuals, 24,638 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90256771 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (gene-based - predicted loss of function) 143,508 European ancestry individuals, 24,628 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256772 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (kernel-based - missense) 143,508 European ancestry individuals, 24,628 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256773 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (gene-based - collapsed missense) 143,508 European ancestry individuals, 24,628 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256774 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (kernel-based - splice) 143,508 European ancestry individuals, 24,628 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256775 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (gene-based - collapsed splice) 143,508 European ancestry individuals, 24,628 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256776 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (gene-based - predicted loss of function) 13,808 European ancestry individuals, 2,214 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256777 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (kernel-based - missense) 13,808 European ancestry individuals, 2,214 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256778 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (gene-based - collapsed missense) 13,808 European ancestry individuals, 2,214 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256779 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (kernel-based - splice) 13,808 European ancestry individuals, 2,214 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256780 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (gene-based - collapsed splice) 13,808 European ancestry individuals, 2,214 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256781 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (gene-based - predicted loss of function) 156,201 European ancestry individuals, 26,747 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256782 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (kernel-based - missense) 156,201 European ancestry individuals, 26,747 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256783 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (gene-based - collapsed missense) 156,201 European ancestry individuals, 26,747 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256784 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (kernel-based - splice) 156,201 European ancestry individuals, 26,747 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256785 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Triglyceride levels (gene-based - collapsed splice) 156,201 European ancestry individuals, 26,747 South Asian, African, East Asian, Hispanic or Latin American, or unknown ancestry individuals NA NR [15702718] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90256786 Exome-wide sequencing 2023-05-30 36450729 Gao XR 2022-11-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36450729 Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma. Intraocular pressure 98,674 European ancestry individuals NA Illumina [NR] 6 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90270075 Exome-wide sequencing 2023-05-30 36450729 Gao XR 2022-11-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36450729 Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma. Intraocular pressure 98,674 European ancestry individuals, 11,586 South Asian ancestry, East Asian ancestry, African ancestry individuals NA Illumina [NR] 7 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90270076 Exome-wide sequencing 2023-06-16 37069360 Duperron MG 2023-04-17 Nat Med www.ncbi.nlm.nih.gov/pubmed/37069360 Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease. Extensive white matter perivascular space burden 9,317 European ancestry cases, 29,281 European ancestry controls NA Affymetrix, Illumina [8783191] (imputed) 21 perivascular space measurement http://www.ebi.ac.uk/efo/EFO_0803382 GCST90244151 Genome-wide genotyping array 2023-06-16 37069360 Duperron MG 2023-04-17 Nat Med www.ncbi.nlm.nih.gov/pubmed/37069360 Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease. Extensive white matter perivascular space burden 9,317 European ancestry cases, 29,281 European ancestry controls, 90 Hispanic cases, 249 Hispanic controls, 38 East Asian ancestry cases, 130 East Asian ancestry controls, 162 African American cases, 555 African American controls 223 cases, 1,525 controls, 705 Japanese ancestry cases, 2,157 Japanese ancestry controls Affymetrix, Illumina [9909063] (imputed) 0 perivascular space measurement http://www.ebi.ac.uk/efo/EFO_0803382 GCST90244152 Genome-wide genotyping array 2023-06-16 37069360 Duperron MG 2023-04-17 Nat Med www.ncbi.nlm.nih.gov/pubmed/37069360 Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease. Extensive basal ganglia perivascular space burden 8,950 European ancestry cases, 29,953 European ancestry controls NA Affymetrix, Illumina [8678455] (imputed) 2 perivascular space measurement http://www.ebi.ac.uk/efo/EFO_0803382 GCST90244153 Genome-wide genotyping array 2023-06-16 37069360 Duperron MG 2023-04-17 Nat Med www.ncbi.nlm.nih.gov/pubmed/37069360 Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease. Extensive basal ganglia perivascular space burden 8,950 European ancestry cases, 29,953 European ancestry controls, 51 Hispanic cases, 161 Hispanic controls, 32 East Asian ancestry cases, 136 East Asian ancestry controls, 156 African American cases, 561 African American controls 167 cases, 1,581 controls, 702 Japanese ancestry cases, 2,160 Japanese ancestry controls Affymetrix, Illumina [9758539] (imputed) 0 perivascular space measurement http://www.ebi.ac.uk/efo/EFO_0803382 GCST90244154 Genome-wide genotyping array 2023-06-16 37069360 Duperron MG 2023-04-17 Nat Med www.ncbi.nlm.nih.gov/pubmed/37069360 Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease. Extensive hippocampal perivascular space burden 9,163 European ancestry cases, 29,708 European ancestry controls NA Affymetrix, Illumina [8713024] (imputed) 3 perivascular space measurement http://www.ebi.ac.uk/efo/EFO_0803382 GCST90244155 Genome-wide genotyping array 2023-06-16 37069360 Duperron MG 2023-04-17 Nat Med www.ncbi.nlm.nih.gov/pubmed/37069360 Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease. Extensive hippocampal perivascular space burden 9,163 European ancestry cases, 29,708 European ancestry controls, 69 Hispanic cases, 270 Hispanic controls, 25 East Asian ancestry cases, 143 East Asian ancestry controls, 82 African American cases, 635 African American controls NA Affymetrix, Illumina [9114638] (imputed) 3 perivascular space measurement http://www.ebi.ac.uk/efo/EFO_0803382 GCST90244156 Genome-wide genotyping array 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (gene-based - predicted loss of function) 13,808 European ancestry individuals NA NR [12793493] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256962 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (kernel-based - missense) 13,808 European ancestry individuals NA NR [12793493] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256963 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (gene-based - collapsed missense) 13,808 European ancestry individuals NA NR [12793493] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256964 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (kernel-based - splice) 13,808 European ancestry individuals NA NR [12793493] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256965 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Rheumatoid factor levels (gene-based - collapsed splice) 13,808 European ancestry individuals NA NR [12793493] 0 rheumatoid factor measurement http://www.ebi.ac.uk/efo/EFO_0005767 GCST90256966 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (gene-based - predicted loss of function) 124,389 European ancestry individuals NA NR [12793493] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256967 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (kernel-based - missense) 124,389 European ancestry individuals NA NR [12793493] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256968 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (gene-based - collapsed missense) 124,389 European ancestry individuals NA NR [12793493] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256969 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (kernel-based - splice) 124,389 European ancestry individuals NA NR [12793493] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256970 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Lipoprotein A levels (gene-based - collapsed splice) 124,389 European ancestry individuals NA NR [12793493] 0 lipoprotein A measurement http://www.ebi.ac.uk/efo/EFO_0006925 GCST90256971 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (gene-based - predicted loss of function) 156,167 European ancestry individuals NA NR [12793493] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256972 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (kernel-based - missense) 156,167 European ancestry individuals NA NR [12793493] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256973 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (gene-based - collapsed missense) 156,167 European ancestry individuals NA NR [12793493] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256974 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (kernel-based - splice) 156,167 European ancestry individuals NA NR [12793493] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256975 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urate levels (gene-based - collapsed splice) 156,167 European ancestry individuals NA NR [12793493] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90256976 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (gene-based - predicted loss of function) 143,508 European ancestry individuals NA NR [12793493] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256977 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (kernel-based - missense) 143,508 European ancestry individuals NA NR [12793493] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256978 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (gene-based - collapsed missense) 143,508 European ancestry individuals NA NR [12793493] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256979 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (kernel-based - splice) 143,508 European ancestry individuals NA NR [12793493] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256980 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Phosphate levels (gene-based - collapsed splice) 143,508 European ancestry individuals NA NR [12793493] 0 blood phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010972 GCST90256981 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (gene-based - predicted loss of function) 156,069 European ancestry individuals NA NR [12793493] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256982 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (kernel-based - missense) 156,069 European ancestry individuals NA NR [12793493] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256983 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (gene-based - collapsed missense) 156,069 European ancestry individuals NA NR [12793493] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256984 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (kernel-based - splice) 156,069 European ancestry individuals NA NR [12793493] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256985 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Direct low density lipoprotein cholesterol levels (gene-based - collapsed splice) 156,069 European ancestry individuals NA NR [12793493] 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90256986 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (gene-based - predicted loss of function) 25,052 European ancestry individuals NA NR [12793493] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256987 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (kernel-based - missense) 25,052 European ancestry individuals NA NR [12793493] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256988 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (gene-based - collapsed missense) 25,052 European ancestry individuals NA NR [12793493] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256989 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (kernel-based - splice) 25,052 European ancestry individuals NA NR [12793493] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256990 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Estradiol levels (gene-based - collapsed splice) 25,052 European ancestry individuals NA NR [12793493] 0 estradiol measurement http://www.ebi.ac.uk/efo/EFO_0004697 GCST90256991 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (gene-based - predicted loss of function) 156,322 European ancestry individuals NA NR [12793493] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256992 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (kernel-based - missense) 156,322 European ancestry individuals NA NR [12793493] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256993 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (gene-based - collapsed missense) 156,322 European ancestry individuals NA NR [12793493] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256994 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (kernel-based - splice) 156,322 European ancestry individuals NA NR [12793493] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256995 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cystatin C levels (gene-based - collapsed splice) 156,322 European ancestry individuals NA NR [12793493] 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90256996 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (gene-based - predicted loss of function) 156,329 European ancestry individuals NA NR [12793493] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256997 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (kernel-based - missense) 156,329 European ancestry individuals NA NR [12793493] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256998 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (gene-based - collapsed missense) 156,329 European ancestry individuals NA NR [12793493] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90256999 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (kernel-based - splice) 156,329 European ancestry individuals NA NR [12793493] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90257000 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Cholesterol levels (gene-based - collapsed splice) 156,329 European ancestry individuals NA NR [12793493] 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90257001 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (gene-based - predicted loss of function) 143,716 European ancestry individuals NA NR [12793493] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90257002 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (kernel-based - missense) 143,716 European ancestry individuals NA NR [12793493] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90257003 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (gene-based - collapsed missense) 143,716 European ancestry individuals NA NR [12793493] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90257004 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (kernel-based - splice) 143,716 European ancestry individuals NA NR [12793493] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90257005 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Calcium levels (gene-based - collapsed splice) 143,716 European ancestry individuals NA NR [12793493] 0 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90257006 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (gene-based - predicted loss of function) 156,223 European ancestry individuals NA NR [12793493] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90257007 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (kernel-based - missense) 156,223 European ancestry individuals NA NR [12793493] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90257008 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (gene-based - collapsed missense) 156,223 European ancestry individuals NA NR [12793493] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90257009 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (kernel-based - splice) 156,223 European ancestry individuals NA NR [12793493] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90257010 Exome-wide sequencing 2023-03-24 36088354 Monti R 2022-09-10 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36088354 Identifying interpretable gene-biomarker associations with functionally informed kernel-based tests in 190,000 exomes. Urea levels (gene-based - collapsed splice) 156,223 European ancestry individuals NA NR [12793493] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90257011 Exome-wide sequencing 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right entorhinal volume (UKB data field 26894) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 entorhinal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010302 GCST90085869 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right frontal pole volume (UKB data field 26920) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 frontal pole volume measurement http://www.ebi.ac.uk/efo/EFO_0010304 GCST90085870 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right fusiform volume (UKB data field 26895) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 fusiform gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010305 GCST90085871 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right hippocampus volume (UKB data field 26593) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90085872 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right inferior parietal volume (UKB data field 26896) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 inferior parietal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010307 GCST90085873 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right inferior temporal volume (UKB data field 26897) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 inferior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010308 GCST90085874 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right insula volume (UKB data field 26922) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 insular cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010309 GCST90085875 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right isthmus cingulate volume (UKB data field 26898) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 isthmus cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010310 GCST90085876 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right lateral occipital volume (UKB data field 26899) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 lateral occipital cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010311 GCST90085877 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right lateral orbitofrontal volume (UKB data field 26900) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 lateral orbital frontal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010312 GCST90085878 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right lingual volume (UKB data field 26901) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 lingual gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010314 GCST90085879 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right medial orbitofrontal volume (UKB data field 26902) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 medial orbital frontal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010315 GCST90085880 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right middle temporal volume (UKB data field 26903) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 middle temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010316 GCST90085881 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right pallidum volume (UKB data field 26592) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pallidum volume http://www.ebi.ac.uk/efo/EFO_0006933 GCST90085882 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right paracentral volume (UKB data field 26905) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 paracentral lobule volume measurement http://www.ebi.ac.uk/efo/EFO_0010317 GCST90085883 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right pars opercularis volume (UKB data field 26906) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pars opercularis volume measurement http://www.ebi.ac.uk/efo/EFO_0010319 GCST90085885 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right pars orbitalis volume (UKB data field 26907) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pars orbitalis volume measurement http://www.ebi.ac.uk/efo/EFO_0010320 GCST90085886 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right pars triangularis volume (UKB data field 26908) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pars triangularis volume measurement http://www.ebi.ac.uk/efo/EFO_0010321 GCST90085887 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right postcentral volume (UKB data field 26910) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 postcentral gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010323 GCST90085889 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right precentral volume (UKB data field 26912) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 precentral gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010325 GCST90085891 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right putamen volume (UKB data field 26591) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 putamen volume http://www.ebi.ac.uk/efo/EFO_0006932 GCST90085893 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left parahippocampal volume (UKB data field 26803) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 parahippocampal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010318 GCST90085843 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left pars opercularis volume (UKB data field 26805) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pars opercularis volume measurement http://www.ebi.ac.uk/efo/EFO_0010319 GCST90085844 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left amygdala volume (UKB data field 26563) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 amygdala volume http://www.ebi.ac.uk/efo/EFO_0006934 GCST90085821 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left pars triangularis volume (UKB data field 26807) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pars triangularis volume measurement http://www.ebi.ac.uk/efo/EFO_0010321 GCST90085846 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left pericalcarine volume (UKB data field 26808) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pericalcarine cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010322 GCST90085847 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left caudate volume (UKB data field 26559) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0004830 GCST90085825 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left posterior cingulate volume (UKB data field 26810) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 posterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010324 GCST90085849 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left precentral volume (UKB data field 26811) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 precentral gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010325 GCST90085850 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left precuneus volume (UKB data field 26812) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 precuneus cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010326 GCST90085851 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left entorhinal volume (UKB data field 26793) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 entorhinal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010302 GCST90085828 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left rostral anterior cingulate volume (UKB data field 26813) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 rostral anterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010327 GCST90085853 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left fusiform volume (UKB data field 26794) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 fusiform gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010305 GCST90085830 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left hippocampus volume (UKB data field 26562) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90085831 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left inferior parietal volume (UKB data field 26795) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 inferior parietal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010307 GCST90085832 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left inferior temporal volume (UKB data field 26796) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 inferior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010308 GCST90085833 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left insula volume (UKB data field 26821) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 insular cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010309 GCST90085834 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left isthmus cingulate volume (UKB data field 26797) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 isthmus cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010310 GCST90085835 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right accumbens area volume (UKB data field 26595) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006931 GCST90085861 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left lateral orbitofrontal volume (UKB data field 26799) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 lateral orbital frontal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010312 GCST90085837 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left lingual volume (UKB data field 26800) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 lingual gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010314 GCST90085838 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left medial orbitofrontal volume (UKB data field 26801) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 medial orbital frontal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010315 GCST90085839 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left middle temporal volume (UKB data field 26802) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 middle temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010316 GCST90085840 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left pallidum volume (UKB data field 26561) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pallidum volume http://www.ebi.ac.uk/efo/EFO_0006933 GCST90085841 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left paracentral volume (UKB data field 26804) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 paracentral lobule volume measurement http://www.ebi.ac.uk/efo/EFO_0010317 GCST90085842 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Brain stem volume (UKB data field 26526) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 brain stem volume measurement http://www.ebi.ac.uk/efo/EFO_0010605 GCST90085819 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left accumbens area volume (UKB data field 26564) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006931 GCST90085820 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left pars orbitalis volume (UKB data field 26806) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pars orbitalis volume measurement http://www.ebi.ac.uk/efo/EFO_0010320 GCST90085845 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left banks of superior temporal sulcus volume (UKB data field 26789) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 banks of the superior temporal sulcus volume measurement http://www.ebi.ac.uk/efo/EFO_0010286 GCST90085822 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left caudal anterior cingulate volume (UKB data field 26790) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 caudal anterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010289 GCST90085823 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left caudal middle frontal volume (UKB data field 26791) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 caudal middle frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010290 GCST90085824 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left postcentral volume (UKB data field 26809) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 postcentral gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010323 GCST90085848 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right cuneus volume (UKB data field 26893) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 cuneus cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010301 GCST90085867 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left cuneus volume (UKB data field 26792) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 cuneus cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010301 GCST90085826 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left ventral diencephalon (DC) volume (UKB data field 26565) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 ventral diencephalon volume measurement http://www.ebi.ac.uk/efo/EFO_0010337 GCST90085827 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left putamen volume (UKB data field 26560) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 putamen volume http://www.ebi.ac.uk/efo/EFO_0006932 GCST90085852 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left frontal pole volume (UKB data field 26819) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 frontal pole volume measurement http://www.ebi.ac.uk/efo/EFO_0010304 GCST90085829 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left rostral middle frontal volume (UKB data field 26814) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 rostral middle frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010328 GCST90085854 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left superior frontal volume (UKB data field 26815) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 superior frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010329 GCST90085855 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left superior parietal volume (UKB data field 26816) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 superior parietal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010330 GCST90085856 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left superior temporal volume (UKB data field 26817) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 superior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010331 GCST90085857 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left supramarginal volume (UKB data field 26818) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 supramarginal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010332 GCST90085858 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left thalamus proper volume (UKB data field 26558) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST90085859 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left transverse temporal volume (UKB data field 26820) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 transverse temporal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010336 GCST90085860 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Left lateral occipital volume (UKB data field 26798) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 lateral occipital cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010311 GCST90085836 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right amygdala volume (UKB data field 26594) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 amygdala volume http://www.ebi.ac.uk/efo/EFO_0006934 GCST90085862 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right banks of superior temporal sulcus volume (UKB data field 26890) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 banks of the superior temporal sulcus volume measurement http://www.ebi.ac.uk/efo/EFO_0010286 GCST90085863 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right caudal anterior cingulate volume (UKB data field 26891) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 caudal anterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010289 GCST90085864 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right caudal middle frontal volume (UKB data field 26892) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 caudal middle frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010290 GCST90085865 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right caudate volume (UKB data field 26590) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0004830 GCST90085866 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right ventral diencephalon (DC) volume (UKB data field 26596) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 ventral diencephalon volume measurement http://www.ebi.ac.uk/efo/EFO_0010337 GCST90085868 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right parahippocampal volume (UKB data field 26904) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 parahippocampal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010318 GCST90085884 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right pericalcarine volume (UKB data field 26909) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 pericalcarine cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010322 GCST90085888 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right posterior cingulate volume (UKB data field 26911) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 posterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010324 GCST90085890 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right precuneus volume (UKB data field 26913) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 precuneus cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010326 GCST90085892 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right rostral anterior cingulate volume (UKB data field 26914) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 rostral anterior cingulate cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010327 GCST90085894 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right rostral middle frontal volume (UKB data field 26915) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 rostral middle frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010328 GCST90085895 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right superior frontal volume (UKB data field 26916) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 superior frontal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010329 GCST90085896 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right superior parietal volume (UKB data field 26917) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 superior parietal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010330 GCST90085897 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right superior temporal volume (UKB data field 26918) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 superior temporal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010331 GCST90085898 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right supramarginal volume (UKB data field 26919) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 supramarginal gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010332 GCST90085899 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right thalamus proper volume (UKB data field 26589) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST90085900 Genome-wide genotyping array 2023-04-19 36987996 Furtjes AE 2023-03-29 Hum Brain Mapp www.ncbi.nlm.nih.gov/pubmed/36987996 General dimensions of human brain morphometry inferred from genome-wide association data. Right transverse temporal volume (UKB data field 26921) 36,778 European ancestry individuals NA Affymetrix [9932682] (imputed) 0 transverse temporal cortex volume measurement http://www.ebi.ac.uk/efo/EFO_0010336 GCST90085901 Genome-wide genotyping array 2023-06-07 36400179 Gautam Y 2022-11-15 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/36400179 Genome-wide admixture and association analysis identifies African ancestry specific risk loci of eosinophilic esophagitis in African American. Eosinophilic esophagitis 137 African American cases, 1,465 African American controls NA Illumina [6000000] (imputed) 57 eosinophilic esophagitis http://www.ebi.ac.uk/efo/EFO_0004232 GCST90270131 Genome-wide genotyping array 2023-08-21 37076872 Zhang Z 2023-04-19 BMC Med www.ncbi.nlm.nih.gov/pubmed/37076872 Genome-wide association analyses identified novel susceptibility loci for pulmonary embolism among Han Chinese population. Pulmonary embolism 622 Han Chinese ancestry cases, 8,853 Han Chinese ancestry controls 646 Han Chinese ancestry cases, 8,810 Han Chinese ancestry controls Illumina [NR] (imputed) 16 pulmonary embolism http://www.ebi.ac.uk/efo/EFO_0003827 GCST90278093 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Abdominal subcutaneous adipose tissue 33,532 European ancestry individuals NA Affymetrix [9061466] (imputed) 1 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST90267347 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Abdominal subcutaneous adipose tissue normalized 32,573 European ancestry individuals NA Affymetrix [9061466] (imputed) 1 subcutaneous adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004766 GCST90267348 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Anterior thigh muscle volume 32,978 European ancestry individuals NA Affymetrix [9061466] (imputed) 7 anterior thigh muscle volume http://www.ebi.ac.uk/efo/EFO_0020935 GCST90267349 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Anterior thigh muscle volume normalized 32,017 European ancestry individuals NA Affymetrix [9061466] (imputed) 0 anterior thigh muscle volume http://www.ebi.ac.uk/efo/EFO_0020935 GCST90267350 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Anterior thigh muscle fat infiltration percentage 32,911 European ancestry individuals NA Affymetrix [9061466] (imputed) 17 anterior thigh muscle fat infiltration measurement http://www.ebi.ac.uk/efo/EFO_0020936 GCST90267351 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Liver proton density fat fraction 33,235 European ancestry individuals NA Affymetrix [9061466] (imputed) 8 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90267352 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Posterior thigh muscle volume 33,022 European ancestry individuals NA Affymetrix [9061466] (imputed) 9 posterior thigh muscle volume http://www.ebi.ac.uk/efo/EFO_0020931 GCST90267353 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Posterior thigh muscle volume normalized 32,059 European ancestry individuals NA Affymetrix [9061466] (imputed) 0 posterior thigh muscle volume http://www.ebi.ac.uk/efo/EFO_0020931 GCST90267354 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Posterior thigh muscle fat infiltration percentage 32,956 European ancestry individuals NA Affymetrix [9061466] (imputed) 24 posterior thigh muscle fat infiltration measurement http://www.ebi.ac.uk/efo/EFO_0020934 GCST90267355 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Total thigh muscle volume z-score 31,977 European ancestry individuals NA Affymetrix [9061466] (imputed) 4 thigh muscle volume http://www.ebi.ac.uk/efo/EFO_0020107 GCST90267356 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Visceral adipose tissue 33,542 European ancestry individuals NA Affymetrix [9061466] (imputed) 2 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90267357 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Visceral adipose tissue normalized 32,564 European ancestry individuals NA Affymetrix [9061466] (imputed) 2 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90267358 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Weight-to-muscle ratio 32,970 European ancestry individuals NA Affymetrix [9061466] (imputed) 1 weight-to-muscle ratio http://www.ebi.ac.uk/efo/EFO_0020099 GCST90267359 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Abdominal fat ratio 32,939 European ancestry individuals NA Affymetrix [9061466] (imputed) 1 abdominal fat ratio http://www.ebi.ac.uk/efo/EFO_0020098 GCST90267360 Genome-wide genotyping array 2023-04-17 36402844 van der Meer D 2022-11-19 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36402844 The link between liver fat and cardiometabolic diseases is highlighted by genome-wide association study of MRI-derived measures of body composition. Body composition (MOSTest) 33,588 European ancestry individuals NA Affymetrix [9100000] (imputed) 77 body composition measurement http://www.ebi.ac.uk/efo/EFO_0005106 GCST90267367 Genome-wide genotyping array 2023-02-22 34215507 Nagakawa S 2021-06-29 Urol Oncol www.ncbi.nlm.nih.gov/pubmed/34215507 The impact of single-nucleotide polymorphisms on intravesical recurrence after bacillus Calmette-Guérin therapy for non-muscle invasive bladder cancer in a genome-wide association study. treatment failure in response to intravesical BCG therapy in non-muscle invasive bladder cancer 14 Japanese ancestry individuals with recurrence, 30 Japanese ancestry individuals without recurrence 29 Japanese ancestry individuals with recurrence, 18 Japanese ancestry individuals without recurrence NR [NR] 0 disease recurrence, response to BCG intravesical immunotherapy http://www.ebi.ac.uk/efo/EFO_0004952, http://www.ebi.ac.uk/efo/EFO_0011041 GCST90032672 Genome-wide genotyping array 2023-03-02 36736436 Bourgault J 2023-01-31 Gastroenterology www.ncbi.nlm.nih.gov/pubmed/36736436 Proteome-wide Mendelian randomization identifies causal links between blood proteins and acute pancreatitis. Acute pancreatitis 10,630 European ancestry cases, 844,679 European ancestry controls NA NR [9570209] (imputed) 13 acute pancreatitis http://www.ebi.ac.uk/efo/EFO_1000652 GCST90255375 Genome-wide genotyping array 2022-12-09 35624721 Liu M 2022-04-27 Antioxidants (Basel) www.ncbi.nlm.nih.gov/pubmed/35624721 A Causal Relationship between Vitamin C Intake with Hyperglycemia and Metabolic Syndrome Risk: A Two-Sample Mendelian Randomization Study. Vitamin C intake 29,398 low vitamin C intake Korean ancestry individuals, 22,729 high vitamin C intake Korean ancestry individuals NA Affymetrix [NR] 0 vitamin C measurement http://www.ebi.ac.uk/efo/EFO_0600003 GCST90131468 Genome-wide genotyping array 2023-03-02 36573383 Gim JA 2022-12-26 J Korean Med Sci www.ncbi.nlm.nih.gov/pubmed/36573383 Demographic and Genome Wide Association Analyses According to Muscle Mass Using Data of the Korean Genome and Epidemiology Study. sarcopenia up to 220 Korean ancestry male cases, up to 169 Korean ancestry male controls NA Affymetrix [500568] 1 sarcopenia http://www.ebi.ac.uk/efo/EFO_1000653 GCST90255390 Genome-wide genotyping array 2023-03-02 36573383 Gim JA 2022-12-26 J Korean Med Sci www.ncbi.nlm.nih.gov/pubmed/36573383 Demographic and Genome Wide Association Analyses According to Muscle Mass Using Data of the Korean Genome and Epidemiology Study. sarcopenia up to 198 Korean ancestry female cases, up to 308 Korean ancestry female controls NA Affymetrix [500568] 4 sarcopenia http://www.ebi.ac.uk/efo/EFO_1000653 GCST90255391 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Chronic kidney disease 2,214 European American ancestry cases, 19,970 European American ancestry controls NA Illumina [6017985] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90128454 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Chronic kidney disease 376 African American cases, 1,583 African American controls NA Illumina [5874655] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90128464 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Chronic nonalcoholic liver disease 3,177 European American ancestry cases, 19,008 European American ancestry controls NA Illumina [6017985] (imputed) 1 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90128455 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Chronic nonalcoholic liver disease 627 East Asian American ancestry cases, 2,660 East Asian American ancestry controls NA Illumina [4806300] (imputed) 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90128458 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Chronic nonalcoholic liver disease 1,466 Hispanic / Latino American cases, 4,490 Hispanic / Latino American controls NA Illumina [6263054] (imputed) 1 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90128461 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Chronic nonalcoholic liver disease 322 African American cases, 1,638 African American controls NA Illumina [5874655] (imputed) 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90128465 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Ischemic heart disease 5,242 European American ancestry cases, 16,943 European American ancestry controls NA Illumina [6017985] (imputed) 1 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90128456 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Ischemic heart disease 649 East Asian American ancestry cases, 2,638 East Asian American ancestry controls NA Illumina [4806300] (imputed) 1 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90128459 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Ischemic heart disease 1,174 Hispanic / Latino American cases, 4,782 Hispanic / Latino American controls NA Illumina [6263054] (imputed) 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90128462 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Ischemic heart disease 514 African American cases, 1,446 African American controls NA Illumina [5874655] (imputed) 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90128466 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Liver/intrahepatic bile duct cancer 197 East Asian American ancestry cases, 3,090 East Asian American ancestry controls NA Illumina [4806300] (imputed) 0 bile duct cancer http://purl.obolibrary.org/obo/MONDO_0003059 GCST90128460 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Liver/intrahepatic bile duct cancer 247 Hispanic / Latino American cases, 5,709 Hispanic / Latino American controls NA Illumina [6263054] (imputed) 1 bile duct cancer http://purl.obolibrary.org/obo/MONDO_0003059 GCST90128463 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Skin cancer 4,583 European American ancestry cases, 17,603 European American ancestry controls NA Illumina [6017985] (imputed) 14 skin neoplasm http://www.ebi.ac.uk/efo/EFO_0004198 GCST90128457 Genome-wide genotyping array 2023-08-23 36085083 Johnson R 2022-09-09 Genome Med www.ncbi.nlm.nih.gov/pubmed/36085083 Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative. Uterine leiomyomata 287 African American cases, 1,674 African American controls NA Illumina [5874655] (imputed) 0 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90128467 Genome-wide genotyping array 2023-01-05 36250097 Chaudhary NS 2022-09-28 Front Med (Lausanne) www.ncbi.nlm.nih.gov/pubmed/36250097 SMOC2 gene interacts with APOL1 in the development of end-stage kidney disease: A genome-wide association study. End stage renal disease x APOL1 risk status (additive) interaction 8,074 African American or Afro-Caribbean individuals 6,791 African American or Afro-Caribbean individuals Illumina [1000000] (imputed) 0 chronic kidney disease, APOL1 risk genotype carrier status http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0009324 GCST90244130 Genome-wide genotyping array 2023-01-05 36250097 Chaudhary NS 2022-09-28 Front Med (Lausanne) www.ncbi.nlm.nih.gov/pubmed/36250097 SMOC2 gene interacts with APOL1 in the development of end-stage kidney disease: A genome-wide association study. End stage renal disease x APOL1 risk status (recessive) interaction 8,074 African American or Afro-Caribbean individuals 6,791 African American or Afro-Caribbean individuals Illumina [1000000] (imputed) 0 chronic kidney disease, APOL1 risk genotype carrier status http://www.ebi.ac.uk/efo/EFO_0003884, http://www.ebi.ac.uk/efo/EFO_0009324 GCST90244131 Genome-wide genotyping array 2022-12-23 35961941 Tanaka Y 2022-08-12 Br J Haematol www.ncbi.nlm.nih.gov/pubmed/35961941 Prominence of NUDT15 genetic variation associated with 6-mercaptopurine tolerance in a genome-wide association study of Japanese children with acute lymphoblastic leukaemia. 6-mercaptopurine dose in acute lymphoblastic leukaemia 224 Japanese ancestry individuals 55 Japanese ancestry individuals Illumina [6236137] (imputed) 2 response to mercaptopurine http://www.ebi.ac.uk/efo/EFO_0007853 GCST90244079 Genome-wide genotyping array 2022-12-15 32163187 Mast AE 2020-03-12 Transfusion www.ncbi.nlm.nih.gov/pubmed/32163187 Genetic and behavioral modification of hemoglobin and iron status among first-time and high-intensity blood donors. High-intensity blood donation (vs. first-time donors) 2,317 European ancestry cases, 38 African ancestry cases, 45 Asian ancestry cases, 24 Hispanic or Latin American cases, 46 cases, 1,674 European ancestry controls NA NR [879000] (imputed) 0 blood donor http://www.ebi.ac.uk/efo/EFO_0009635 GCST90244014 Genome-wide genotyping array 2023-02-28 36660475 Liu X 2022-12-22 iScience www.ncbi.nlm.nih.gov/pubmed/36660475 Sex differences in the oral microbiome, host traits, and their causal relationships. Saliva microbiota abundance 845 Chinese ancestry men, 1,070 Chinese ancestry women 615 Chinese ancestry men, 676 Chinese ancestry women NR [10000000] 0 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90255365 Genome-wide sequencing 2023-02-28 36660475 Liu X 2022-12-22 iScience www.ncbi.nlm.nih.gov/pubmed/36660475 Sex differences in the oral microbiome, host traits, and their causal relationships. Tongue dorsum microbiota abundance 862 Chinese ancestry men, 1,142 Chinese ancestry women 631 Chinese ancestry men, 696 Chinese ancestry women NR [10000000] 0 oral microbiome measurement http://www.ebi.ac.uk/efo/EFO_0801229 GCST90255364 Genome-wide sequencing 2023-02-28 36672803 Xu H 2022-12-24 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36672803 Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium. Ischemic stroke 7,921 European ancestry cases, 9,911 European ancestry controls, 1,044 African American cases, 1,353 African American controls, 756 cases, 1,081 controls 5,874 European ancestry cases, 117,442 European ancestry controls Illumina [106101] 0 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90255376 Genome-wide genotyping array 2023-03-08 36777997 Partanen JJ 2022-10-12 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777997 Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics. Idiopathic pulmonary fibrosis 169 African American or Afro-Caribbean, African ancestry cases, 8,368 African American or Afro-Caribbean, African ancestry controls, 1,210 East Asian ancestry cases, 254,409 East Asian ancestry controls, 6,743 European ancestry cases, 1,056,693 European ancestry controls, 319 Hispanic or Latin American cases, 14,452 Hispanic or Latin American controls, 51 South Asian ancestry cases, 21,897 South Asian ancestry controls NA NR [66600000] (imputed) 0 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST90255646 Genome-wide genotyping array 2023-03-08 36777997 Partanen JJ 2022-10-12 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777997 Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis genetics. Idiopathic pulmonary fibrosis 169 African American or Afro-Caribbean, African ancestry cases, 8,368 African American or Afro-Caribbean, African ancestry controls, 1,210 East Asian ancestry cases, 254,409 East Asian ancestry controls, 9,411 European ancestry cases, 1,057,284 European ancestry controls, 319 Hispanic or Latin American cases, 14,452 Hispanic or Latin American controls, 51 South Asian ancestry cases, 21,897 South Asian ancestry controls NA NR [10800000] (imputed) 25 idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000768 GCST90255647 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs population) 1,703 European ancestry male cases, 208,248 European ancestry male controls NA NR [9738712] (imputed) 21 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104739 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs population) 376 South Asian, African or unknown ancestry cases, 27,694 South Asian, African or unknown ancestry controls NA NR [13688038] (imputed) 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104740 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs tested, not hospitalized) 2,884 European ancestry cases, 95,493 European ancestry controls, 376 South Asian, African or unknown ancestry cases, 6,163 South Asian, African or unknown ancestry controls NA NR [9874253] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104741 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs tested, not hospitalized) 1,181 European ancestry female cases, 51,834 European ancestry female controls, 162 South Asian, African or unknown ancestry female cases, 3,317 South Asian, African or unknown ancestry female controls NA NR [9891263] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104742 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs tested, not hospitalized) 1,703 European ancestry male cases, 43,659 European ancestry male controls, 214 South Asian, African or unknown ancestry male cases, 2,846 South Asian, African or unknown ancestry male controls NA NR [9858058] (imputed) 28 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104743 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs tested, not hospitalized) 2,884 European ancestry cases, 95,493 European ancestry controls NA NR [9740292] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104744 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs tested, not hospitalized) 1,181 European ancestry female cases, 51,834 European ancestry female controls NA NR [9740423] (imputed) 21 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104745 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs tested, not hospitalized) 1,703 European ancestry male cases, 43,659 European ancestry male controls NA NR [9739228] (imputed) 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104746 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs tested, not hospitalized) 376 South Asian, African or unknown ancestry cases, 6,163 South Asian, African or unknown ancestry controls NA NR [13872015] (imputed) 27 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104747 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs not hospitalized) 2,884 European ancestry cases, 13,667 European ancestry controls, 376 South Asian, African or unknown ancestry cases, 1,554 South Asian, African or unknown ancestry controls NA NR [10061349] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104748 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs not hospitalized) 1,181 European ancestry female cases, 7,586 European ancestry female controls, 162 South Asian, African or unknown ancestry female cases, 828 South Asian, African or unknown ancestry female controls NA NR [10107429] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104749 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs not hospitalized) 1,703 European ancestry male cases, 6,081 European ancestry male controls, 214 South Asian, African or unknown ancestry male cases, 726 South Asian, African or unknown ancestry male controls NA NR [10016524] (imputed) 27 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104750 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs not hospitalized) 2,884 European ancestry cases, 13,667 European ancestry controls NA NR [9738843] (imputed) 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104751 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs not hospitalized) 1,181 European ancestry female cases, 7,586 European ancestry female controls NA NR [9739280] (imputed) 24 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104752 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs not hospitalized) 1,703 European ancestry male cases, 6,081 European ancestry male controls NA NR [9739477] (imputed) 18 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104753 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs not hospitalized) 376 South Asian, African or unknown ancestry cases, 1,554 South Asian, African or unknown ancestry controls NA NR [13851307] (imputed) 36 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104754 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs population) 1,120 European ancestry cases, 458,130 European ancestry controls, 124 cases, 27,946 controls NA NR [9857262] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104755 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs population) 387 European ancestry female cases, 248,912 European ancestry female controls, 52 female cases, 14,878 female controls NA NR [9866514] (imputed) 11 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104756 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs population) 733 European ancestry male cases, 209,218 European ancestry male controls, 72 male cases, 13,068 male controls NA NR [9846957] (imputed) 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104757 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs population) 1,120 European ancestry cases, 458,130 European ancestry controls NA NR [9739344] (imputed) 19 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104758 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs population) 387 European ancestry female cases, 248,912 European ancestry female controls NA NR [9739651] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104759 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs population) 733 European ancestry male cases, 209,218 European ancestry male controls NA NR [9738712] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104760 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs tested, not severe) 1,120 European ancestry cases, 79,439 European ancestry controls, 124 cases, 5,303 controls NA NR [9876511] (imputed) 25 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104761 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs tested, not severe) 387 European ancestry female cases, 42,973 European ancestry female controls, 52 female cases, 2,838 female controls NA NR [9896033] (imputed) 11 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104762 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs tested, not severe) 733 European ancestry male cases, 36,466 European ancestry male controls, 72 male cases, 2,465 male controls NA NR [9857703] (imputed) 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104763 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 557 African ancestry cases, 7,087 African ancestry controls, 16,551 European ancestry cases, 442,699 European ancestry controls, 810 South Asian ancestry cases, 8,607 South Asian ancestry controls, 563 cases, 10,446 controls NA NR [9857262] (imputed) 34 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104714 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 316 African ancestry female cases, 4,043 African ancestry female controls, 8,767 European ancestry female cases, 240,532 European ancestry female controls, 351 South Asian ancestry female cases, 3,980 South Asian ancestry female controls, 323 female cases, 5,917 female controls NA NR [9866514] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104715 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 241 African ancestry male cases, 3,044 African ancestry male controls, 7,784 European ancestry male cases, 202,167 European ancestry male controls, 459 South Asian ancestry male cases, 4,627 South Asian ancestry male controls, 240 male cases, 4,529 male controls NA NR [9846957] (imputed) 24 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104716 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 16,551 European ancestry cases, 442,699 European ancestry controls NA NR [9739344] (imputed) 28 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104717 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 8,767 European ancestry female cases, 240,532 European ancestry female controls NA NR [9739651] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104718 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 7,784 European ancestry male cases, 202,167 European ancestry male controls NA NR [9738712] (imputed) 23 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104719 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 810 South Asian ancestry cases, 8,607 South Asian ancestry controls NA NR [9837337] (imputed) 15 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104720 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 557 African ancestry cases, 7,087 African ancestry controls NA NR [15511840] (imputed) 42 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104721 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 563 cases, 10,446 controls NA NR [12057477] (imputed) 13 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104722 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 1,930 South Asian, African or unknown ancestry cases, 26,140 South Asian, African or unknown ancestry controls NA NR [13688038] (imputed) 43 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104723 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 557 African ancestry cases, 1,281 African ancestry controls, 16,551 European ancestry cases, 81,826 European ancestry controls, 810 South Asian ancestry cases, 1,516 South Asian ancestry controls, 563 cases, 1,812 controls NA NR [9874253] (imputed) 27 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104724 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 316 African ancestry female cases, 759 African ancestry female controls, 8,767 European ancestry female cases, 44,248 European ancestry female controls, 351 South Asian ancestry female cases, 695 South Asian ancestry female controls, 323 female cases, 1,035 female controls NA NR [9891263] (imputed) 22 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104725 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 241 African ancestry male cases, 522 African ancestry male controls, 7,784 European ancestry male cases, 37,578 European ancestry male controls, 459 South Asian ancestry male cases, 821 South Asian ancestry male controls, 240 male cases, 777 male controls NA NR [9858058] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104726 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 16,551 European ancestry cases, 81,826 European ancestry controls NA NR [9738966] (imputed) 20 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104727 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 8,767 European ancestry female cases, 44,248 European ancestry female controls NA NR [9739117] (imputed) 16 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104728 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 7,784 European ancestry male cases, 37,578 European ancestry male controls NA NR [9738416] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104729 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 810 South Asian ancestry cases, 1,516 South Asian ancestry controls NA NR [9843264] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104730 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 557 African ancestry cases, 1,281 African ancestry controls NA NR [15500677] (imputed) 31 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104731 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 563 cases, 1,812 controls NA NR [12315561] (imputed) 27 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104732 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (covid vs negative) 1,930 South Asian, African or unknown ancestry cases, 4,609 South Asian, African or unknown ancestry controls NA NR [13780021] (imputed) 32 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104733 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs population) 2,884 European ancestry cases, 456,366 European ancestry controls, 376 South Asian, African or unknown ancestry cases, 27,694 South Asian, African or unknown ancestry controls NA NR [9857262] (imputed) 24 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104734 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs population) 1,181 European ancestry female cases, 248,118 European ancestry female controls, 162 South Asian, African or unknown ancestry female cases, 14,768 South Asian, African or unknown ancestry female controls NA NR [9866514] (imputed) 23 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104735 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs population) 1,703 European ancestry male cases, 208,248 European ancestry male controls, 214 South Asian, African or unknown ancestry male cases, 12,926 South Asian, African or unknown ancestry male controls NA NR [9846957] (imputed) 26 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104736 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs population) 2,884 European ancestry cases, 456,366 European ancestry controls NA NR [9739344] (imputed) 30 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104737 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (hospitalized vs population) 1,181 European ancestry female cases, 248,118 European ancestry female controls NA NR [9739651] (imputed) 25 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104738 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle systole) 27,156 British ancestry individuals NA Affymetrix [4485863] (imputed) 5 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258659 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle diastole) 27,074 British ancestry individuals NA Affymetrix [4485863] (imputed) 1 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258660 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle systole) 27,156 British ancestry individuals, 368 South Asian ancestry individuals, 222 African ancestry individuals, 85 East Asian ancestry individuals NA Affymetrix [4485863] (imputed) 8 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258661 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle diastole) 27,074 British ancestry individuals, 368 South Asian ancestry individuals, 222 African ancestry individuals, 85 East Asian ancestry individuals NA Affymetrix [4485863] (imputed) 4 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258662 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle systole) 222 African ancestry individuals NA Affymetrix [4485863] (imputed) 3 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258663 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle diastole) 222 African ancestry individuals NA Affymetrix [4485863] (imputed) 3 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258664 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle systole) 85 East Asian ancestry individuals NA Affymetrix [4485863] (imputed) 1 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258665 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle diastole) 85 East Asian ancestry individuals NA Affymetrix [4485863] (imputed) 2 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258666 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle systole) 368 South Asian ancestry individuals NA Affymetrix [4485863] (imputed) 3 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258667 Genome-wide genotyping array 2023-04-17 35132965 Yu M 2022-02-08 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35132965 Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. Mitral valve annular diameter (left ventricle diastole) 368 South Asian ancestry individuals NA Affymetrix [4485863] (imputed) 4 mitral valve annular diameter http://www.ebi.ac.uk/efo/EFO_0020096 GCST90258668 Genome-wide genotyping array 2023-02-23 36320039 D'Urso S 2022-11-01 BMC Med www.ncbi.nlm.nih.gov/pubmed/36320039 Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk. Age at last live birth 203,153 European ancestry individuals NA NR [18557407] (imputed) 11 age at last pregnancy measurement http://www.ebi.ac.uk/efo/EFO_0009440 GCST90244702 Genome-wide genotyping array 2023-02-23 36320039 D'Urso S 2022-11-01 BMC Med www.ncbi.nlm.nih.gov/pubmed/36320039 Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk. Years taking oral contraceptive pill 178,233 European ancestry individuals NA NR [18557407] (imputed) 0 contraception http://www.ebi.ac.uk/efo/EFO_0009520 GCST90244703 Genome-wide genotyping array 2023-02-23 36320039 D'Urso S 2022-11-01 BMC Med www.ncbi.nlm.nih.gov/pubmed/36320039 Mendelian randomization analysis of factors related to ovulation and reproductive function and endometrial cancer risk. Years ovulating 118,227 European ancestry individuals NA NR [18557407] (imputed) 19 ovulation http://purl.obolibrary.org/obo/GO_0030728 GCST90244704 Genome-wide genotyping array 2023-02-16 36539420 Xiong Z 2022-12-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36539420 Combining genome-wide association studies highlight novel loci involved in human facial variation. Facial morphology (multitrait analysis) 10,115 European ancestry individuals 3,948 European ancestry individuals, 9,674 Chinese ancestry individuals NR [NR] 30 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90250819 Genome-wide genotyping array 2023-02-17 33956999 Zeng H 2021-05-06 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/33956999 Type 2 diabetes is causally associated with reduced serum osteocalcin: A genome-wide association and Mendelian randomization study. Serum 25-Hydroxyvitamin D levels 4,269 East Asian ancestry individuals 396 East Asian ancestry individuals Illumina [8604360] (imputed) 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90250821 Genome-wide genotyping array 2023-02-17 33956999 Zeng H 2021-05-06 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/33956999 Type 2 diabetes is causally associated with reduced serum osteocalcin: A genome-wide association and Mendelian randomization study. Serum parathyroid hormone levels 4,250 East Asian ancestry individuals 396 East Asian ancestry individuals Illumina [8604360] (imputed) 0 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST90250822 Genome-wide genotyping array 2023-02-17 33956999 Zeng H 2021-05-06 J Bone Miner Res www.ncbi.nlm.nih.gov/pubmed/33956999 Type 2 diabetes is causally associated with reduced serum osteocalcin: A genome-wide association and Mendelian randomization study. Serum osteocalcin levels 4,260 East Asian ancestry individuals 396 East Asian ancestry individuals Illumina [8604360] (imputed) 0 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90250823 Genome-wide genotyping array 2023-03-01 36546557 Sadler KV 2022-12-22 Brain www.ncbi.nlm.nih.gov/pubmed/36546557 Genome-wide association analysis identifies a susceptibility locus for sporadic vestibular schwannoma at 9p21. Sporadic vestibular schwannoma 911 British ancestry cases, 5,500 British ancestry controls NA Affymetrix [492266] (imputed) 1 Vestibular schwannoma http://purl.obolibrary.org/obo/HP_0009588 GCST90134433 Genome-wide genotyping array 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Maximum measurement of hepatic fat 2,814 African ancestry individuals NA NR [NR] 1 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255377 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Median measurement of hepatic fat 2,814 African ancestry individuals NA NR [NR] 5 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255378 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Minimum measurement of hepatic fat 2,814 African ancestry individuals NA NR [NR] 5 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255379 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Maximum measurement of hepatic fat 7,096 European ancestry individuals NA NR [NR] 9 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255380 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Median measurement of hepatic fat 7,096 European ancestry individuals NA NR [NR] 7 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255381 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Minimum measurement of hepatic fat 7,096 European ancestry individuals NA NR [NR] 6 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255382 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Maximum measurement of hepatic fat 2,814 African ancestry individuals, 7,096 European ancestry individuals, 113 Hispanic or Latin American individuals, 103 East Asian ancestry individuals, 84 South Asian ancestry individuals NA NR [NR] 2 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255383 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Median measurement of hepatic fat 2,814 African ancestry individuals, 7,096 European ancestry individuals, 113 Hispanic or Latin American individuals, 103 East Asian ancestry individuals, 84 South Asian ancestry individuals NA NR [NR] 5 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255384 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Minimum measurement of hepatic fat 2,814 African ancestry individuals, 7,096 European ancestry individuals, 113 Hispanic or Latin American individuals, 103 East Asian ancestry individuals, 84 South Asian ancestry individuals NA NR [NR] 4 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255385 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Maximum measurement of hepatic fat 2,814 African ancestry individuals, 7,096 European ancestry individuals, 113 Hispanic or Latin American individuals, 103 East Asian ancestry individuals, 84 South Asian ancestry individuals NA NR [NR] 7 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255386 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Median measurement of hepatic fat 2,814 African ancestry individuals, 7,096 European ancestry individuals, 113 Hispanic or Latin American individuals, 103 East Asian ancestry individuals, 84 South Asian ancestry individuals NA NR [NR] 9 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255387 Exome-wide sequencing 2023-03-02 36513072 Park J 2022-12-12 Cell Rep Med www.ncbi.nlm.nih.gov/pubmed/36513072 Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobank. Minimum measurement of hepatic fat 2,814 African ancestry individuals, 7,096 European ancestry individuals, 113 Hispanic or Latin American individuals, 103 East Asian ancestry individuals, 84 South Asian ancestry individuals NA NR [NR] 6 liver fat measurement http://www.ebi.ac.uk/efo/EFO_0010821 GCST90255388 Exome-wide sequencing 2022-12-22 35951648 Gillespie NA 2022-08-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35951648 Determining the stability of genome-wide factors in BMI between ages 40 to 69 years. Body mass index (age 40-44) 34,001 individuals NA NR [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244072 Genome-wide genotyping array 2022-12-22 35951648 Gillespie NA 2022-08-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35951648 Determining the stability of genome-wide factors in BMI between ages 40 to 69 years. Body mass index (age 45-49) 45,294 individuals NA NR [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244073 Genome-wide genotyping array 2022-12-22 35951648 Gillespie NA 2022-08-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35951648 Determining the stability of genome-wide factors in BMI between ages 40 to 69 years. Body mass index (age 50-54) 53,602 individuals NA NR [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244074 Genome-wide genotyping array 2022-12-22 35951648 Gillespie NA 2022-08-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35951648 Determining the stability of genome-wide factors in BMI between ages 40 to 69 years. Body mass index (age 55-59) 64,891 individuals NA NR [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244075 Genome-wide genotyping array 2022-12-22 35951648 Gillespie NA 2022-08-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35951648 Determining the stability of genome-wide factors in BMI between ages 40 to 69 years. Body mass index (age 60-64) 89,824 individuals NA NR [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244076 Genome-wide genotyping array 2022-12-22 35951648 Gillespie NA 2022-08-11 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/35951648 Determining the stability of genome-wide factors in BMI between ages 40 to 69 years. Body mass index (age 65-73) 71,178 individuals NA NR [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244077 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hyperlipidemia (number of purchases) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 73 antihyperlipidemic drug use measurement http://www.ebi.ac.uk/efo/EFO_0803367 GCST90250902 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hyperlipidemia (changing simvastatin to another statin) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 antihyperlipidemic drug use measurement http://www.ebi.ac.uk/efo/EFO_0803367 GCST90250903 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hyperlipidemia (fast discontinuation of statin use) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 antihyperlipidemic drug use measurement http://www.ebi.ac.uk/efo/EFO_0803367 GCST90250904 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hypertension (number of purchases) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 181 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90250905 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hypertension (more than one antihypertensive group) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90250906 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hypertension (more than two antihypertensive group) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90250907 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hypertension (more than three antihypertensive group) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90250908 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hypertension (all five antihypertensive groups) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90250909 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for hypertension (fast discontinuation of hypertension medication use) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90250910 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for T2D (number of purchases) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 77 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90250911 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for T2D (use of second-line agents) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90250912 Genome-wide genotyping array 2023-03-08 36653479 Kiiskinen T 2023-01-18 Nat Med www.ncbi.nlm.nih.gov/pubmed/36653479 Genetic predictors of lifelong medication-use patterns in cardiometabolic diseases. Medication use for T2D (use of insulin) 567,671 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 0 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90250913 Genome-wide genotyping array 2023-01-20 36329495 Cai L 2022-11-03 J Transl Med www.ncbi.nlm.nih.gov/pubmed/36329495 Evidence that the pituitary gland connects type 2 diabetes mellitus and schizophrenia based on large-scale trans-ethnic genetic analyses. Type 2 diabetes or schizophrenia (pleiotropy) 77,418 East Asian ancestry type 2 diabetes cases, 22,778 East Asian ancestry schizophrenia cases, 391,484 East Asian ancestry controls, 74,124 European ancestry type 2 diabetes cases, 33,640 European ancestry schizophrenia cases, 867,462 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 25 schizophrenia, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005090, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90244709 Genome-wide genotyping array 2023-04-13 36973338 Soo CC 2023-03-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36973338 Genome-wide association study of population-standardised cognitive performance phenotypes in a rural South African community. Executive function 1,887 Sub-Saharan African ancestry individuals NA Illumina [13972012] (imputed) 19 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90246328 Genome-wide genotyping array 2023-04-13 36973338 Soo CC 2023-03-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36973338 Genome-wide association study of population-standardised cognitive performance phenotypes in a rural South African community. Language performance 1,887 Sub-Saharan African ancestry individuals NA Illumina [13972012] (imputed) 21 language measurement http://www.ebi.ac.uk/efo/EFO_0007797 GCST90246329 Genome-wide genotyping array 2023-04-13 36973338 Soo CC 2023-03-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36973338 Genome-wide association study of population-standardised cognitive performance phenotypes in a rural South African community. Episodic memory 1,887 Sub-Saharan African ancestry individuals NA Illumina [13972012] (imputed) 21 episodic memory http://www.ebi.ac.uk/efo/EFO_0004333 GCST90246330 Genome-wide genotyping array 2023-04-13 36973338 Soo CC 2023-03-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36973338 Genome-wide association study of population-standardised cognitive performance phenotypes in a rural South African community. Cognitive function 2,211 Sub-Saharan African ancestry individuals NA Illumina [13972012] (imputed) 17 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90246331 Genome-wide genotyping array 2023-04-13 36973338 Soo CC 2023-03-27 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36973338 Genome-wide association study of population-standardised cognitive performance phenotypes in a rural South African community. Visuospatial ability 1,887 Sub-Saharan African ancestry individuals NA Illumina [13972012] (imputed) 16 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90246332 Genome-wide genotyping array 2023-08-16 37124606 Douville NJ 2023-04-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/37124606 Genetic predisposition may not improve prediction of cardiac surgery-associated acute kidney injury. Cardiac surgery-associated acute kidney injury 1,970 European ancestry individuals NA Illumina [6291460] (imputed) 6 post-operative acute kidney injury http://www.ebi.ac.uk/efo/EFO_0009955 GCST90277552 Genome-wide genotyping array 2023-06-07 36375000 Lawless D 2022-11-15 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/36375000 Viral genetic determinants of prolonged respiratory syncytial virus infection among infants in a healthy term birth cohort. Respiratory syncytial virus infection 509 European, African American, Hispanic ancestry cases, 112 European, African American, Hispanic ancestry controls NA Illumina [680526] 0 Respiratory Syncytial Virus Infection http://www.ebi.ac.uk/efo/EFO_1001413 GCST90270132 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs tested, not severe) 1,120 European ancestry cases, 79,439 European ancestry controls NA NR [9738322] (imputed) 19 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104764 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs tested, not severe) 387 European ancestry female cases, 42,973 European ancestry female controls NA NR [9738866] (imputed) 16 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104765 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs tested, not severe) 733 European ancestry male cases, 36,466 European ancestry male controls NA NR [9738548] (imputed) 14 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104766 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs non-severe with positive test) 1,120 European ancestry cases, 14,695 European ancestry controls, 124 cases, 1,718 controls NA NR [10058208] (imputed) 13 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104767 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs non-severe with positive test) 387 European ancestry female cases, 7,976 European ancestry female controls, 52 female cases, 890 female controls NA NR [10099777] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104768 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs non-severe with positive test) 733 European ancestry male cases, 6,719 European ancestry male controls, 72 male cases, 828 male controls NA NR [10019301] (imputed) 17 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104769 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs non-severe with positive test) 1,120 European ancestry cases, 14,695 European ancestry controls NA NR [9738162] (imputed) 13 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104770 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs non-severe with positive test) 387 European ancestry female cases, 7,976 European ancestry female controls NA NR [9737389] (imputed) 16 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104771 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 (severe vs non-severe with positive test) 733 European ancestry male cases, 6,719 European ancestry male controls NA NR [9738857] (imputed) 14 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104772 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 death (death vs population) 1,001 European ancestry cases, 458,249 European ancestry controls, 103 cases, 27,967 controls NA NR [9857262] (imputed) 25 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90104773 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 death (death vs population) 1,001 European ancestry cases, 458,249 European ancestry controls NA NR [9739344] (imputed) 23 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90104774 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 death (death vs tested and survived) 1,001 European ancestry cases, 79,558 European ancestry controls, 103 cases, 5,324 controls NA NR [9876511] (imputed) 25 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90104775 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. COVID-19 death (death vs tested and survived) 1,001 European ancestry cases, 79,558 European ancestry controls NA NR [9738322] (imputed) 17 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90104776 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. Mortality in COVID-19 1,001 European ancestry cases with COVID-19, 14,814 European ancestry controls with COVID-19, 103 cases with COVID-19, 1,739 controls with COVID-19 NA NR [10058208] (imputed) 22 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90104777 Genome-wide genotyping array 2023-01-09 35224516 Thibord F 2022-02-22 HGG Adv www.ncbi.nlm.nih.gov/pubmed/35224516 A year of COVID-19 GWAS results from the GRASP portal reveals potential genetic risk factors. Mortality in COVID-19 1,001 European ancestry cases with COVID-19, 14,814 European ancestry controls with COVID-19 NA NR [9738162] (imputed) 18 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90104778 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Physical activity (standard GWA) 271,843 European ancestry individuals NA NR [7296989] (imputed) 3 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90267292 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Physical activity (weighted GWA) 98,035 European ancestry individuals NA NR [7296989] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90267293 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. UK Biobank participation probability (standard GWA) 283,749 European ancestry individuals NA NR [7296935] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90267294 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. UK Biobank participation probability (weighted GWA) 102,215 European ancestry individuals NA NR [7296935] (imputed) 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90267295 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Reaction time (standard GWA) 282,217 European ancestry individuals NA NR [7296904] (imputed) 15 reaction time measurement http://www.ebi.ac.uk/efo/EFO_0008393 GCST90267296 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Reaction time (weighted GWA) 101,556 European ancestry individuals NA NR [7296904] (imputed) 1 reaction time measurement http://www.ebi.ac.uk/efo/EFO_0008393 GCST90267297 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Risk taking (standard GWA) 274,537 European ancestry individuals NA NR [7296828] (imputed) 8 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST90267298 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Risk taking (weighted GWA) 99,063 European ancestry individuals NA NR [7296828] (imputed) 1 risk-taking behaviour http://www.ebi.ac.uk/efo/EFO_0008579 GCST90267299 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Sex (standard GWA) 283,749 European ancestry individuals NA NR [7296935] (imputed) 0 biological sex http://purl.obolibrary.org/obo/PATO_0000047 GCST90267300 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Alcohol frequency weekly (standard GWA) 283,162 European ancestry individuals NA NR [7296933] (imputed) 25 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90267266 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Sex (weigthed GWA) 102,215 European ancestry individuals NA NR [7296935] (imputed) 0 biological sex http://purl.obolibrary.org/obo/PATO_0000047 GCST90267301 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Smoking status (standard GWA) 283,749 European ancestry individuals NA NR [7296935] (imputed) 45 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90267302 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Smoking status (weighted GWA) 102,215 European ancestry individuals NA NR [7296935] (imputed) 7 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90267303 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Systolic blood pressure (standard GWA) 275,793 European ancestry individuals NA NR [7296885] (imputed) 131 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90267304 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Systolic blood pressure (weighted GWA) 99,220 European ancestry individuals NA NR [7296885] (imputed) 31 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90267305 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Vegetable intake (standard GWA) 276,203 European ancestry individuals NA NR [7296955] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90267306 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Vegetable intake (weighted GWA) 100,090 European ancestry individuals NA NR [7296955] (imputed) 0 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90267307 Genome-wide genotyping array 2023-03-10 36685848 Pinakhina D 2023-01-04 Front Genet www.ncbi.nlm.nih.gov/pubmed/36685848 GWAS of depression in 4,520 individuals from the Russian population highlights the role of MAGI2 (S-SCAM) in the gut-brain axis. Depression 4,520 Russian ancestry individuals NA Illumina [NR] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90255679 Genome-wide genotyping array 2023-03-01 36790221 Wills C 2023-02-15 Genes Chromosomes Cancer www.ncbi.nlm.nih.gov/pubmed/36790221 Germline variation in RASAL2 may predict survival in patients with RAS-activated colorectal cancer. Overall survival in advanced MAPK-activated colorectal cancer 694 European ancestry individuals NA Affymetrix [2789925] (imputed) 0 colorectal cancer, overall survival http://purl.obolibrary.org/obo/MONDO_0005575, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90244553 Genome-wide genotyping array 2023-05-23 36914876 Rahmioglu N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914876 The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Endometriosis 21,779 European ancestry cases, 449,087 European ancestry controls, 1,713 Japanese ancestry cases, 1,581 Japanese ancestry controls NA Affymetrix, Illumina [8593419] (imputed) 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90205183 Genome-wide genotyping array 2023-05-23 36914876 Rahmioglu N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914876 The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Endometriosis 58,961 European ancestry cases, 700,345 European ancestry controls, 1,713 Japanese ancestry cases, 1,581 Japanese ancestry controls NA Affymetrix, Illumina [8163508] (imputed) 177 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90258638 Genome-wide genotyping array 2023-05-23 36914876 Rahmioglu N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914876 The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Endometriosis (stage 3 or 4) 4,045 European ancestry cases, 379,890 European ancestry controls NA NR [10401531] (imputed) 13 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90258639 Genome-wide genotyping array 2023-05-23 36914876 Rahmioglu N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914876 The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Endometriosis (stage 1 or 2) 3,916 European ancestry cases, 184,006 European ancestry controls NA NR [10401531] (imputed) 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90258640 Genome-wide genotyping array 2023-05-23 36914876 Rahmioglu N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914876 The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Endometriosis-associated infertility 3,060 European ancestry cases, 242,555 European ancestry controls NA NR [10401531] (imputed) 2 female infertility, endometriosis http://www.ebi.ac.uk/efo/EFO_0008560, http://www.ebi.ac.uk/efo/EFO_0001065 GCST90258641 Genome-wide genotyping array 2023-05-23 36914876 Rahmioglu N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914876 The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Endometriosis (MTAG) 1,248,262 European ancestry individuals NA NR [5945867] (imputed) 52 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90258642 Genome-wide genotyping array 2023-05-23 36914876 Rahmioglu N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914876 The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions. Endometriosis 21,779 European ancestry cases, 449,087 European ancestry controls NA Affymetrix, Illumina [8535826] (imputed) 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90269970 Genome-wide genotyping array 2023-08-15 37388819 Munsch G 2023-06-28 NAR Genom Bioinform www.ncbi.nlm.nih.gov/pubmed/37388819 Genome-wide association study of a semicontinuous trait: illustration of the impact of the modeling strategy through the study of Neutrophil Extracellular Traps levels. Plasma neutrophil extracellular trap levels 657 European ancestry individuals NA Illumina [9670724] (imputed) 1 neutrophil extracellular trap measurement http://www.ebi.ac.uk/efo/EFO_0021775 GCST90137414 Genome-wide genotyping array 2023-08-09 36749126 Zhou XJ 2023-02-02 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/36749126 Genome-wide Association Study in Acute Tubulointerstitial Nephritis. Acute tubulointerstitial nephritis 544 Chinese ancestry cases, 2,346 Chinese ancestry controls NA NR [NR] (imputed) 2 Acute tubulointerstitial nephritis http://purl.obolibrary.org/obo/HP_0004729 GCST90270294 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at lumbar spine (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90261370 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right total hip (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261371 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left total hip (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261372 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right femoral neck (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261373 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left femoral neck (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261374 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right trochanter (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261375 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left trochanter (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261376 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right intertrochanter (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261377 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left intertrochanter (model 1) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261378 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at lumbar spine (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90261379 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right total hip (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261380 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left total hip (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261381 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right femoral neck (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261382 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left femoral neck (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261383 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right trochanter (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261384 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left trochanter (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261385 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right intertrochanter (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261386 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left intertrochanter (model 1) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261387 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at lumbar spine (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90261388 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right total hip (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261389 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left total hip (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261390 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right femoral neck (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261391 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left femoral neck (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261392 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right trochanter (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261393 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left trochanter (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261394 Genome-wide genotyping array 2023-02-22 34572079 Yang NI 2021-09-15 Cells www.ncbi.nlm.nih.gov/pubmed/34572079 Artificial Intelligence-Assisted Identification of Genetic Factors Predisposing High-Risk Individuals to Asymptomatic Heart Failure. Asymptomatic heart failure in heart failure risk 34 East Asian ancestry asymptomatic high-risk cases, 83 East Asian ancestry high-risk controls NA NR [392885] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90250820 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right trochanter (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261420 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left trochanter (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261421 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right intertrochanter (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261422 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left intertrochanter (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261423 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right intertrochanter (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261395 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left intertrochanter (model 1) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261396 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at lumbar spine (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90261397 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right total hip (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261398 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left total hip (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261399 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right femoral neck (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 2 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261400 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left femoral neck (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261401 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right trochanter (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 3 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261402 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left trochanter (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 4 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261403 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right intertrochanter (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261404 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left intertrochanter (model 2) 5,428 Chinese ancestry individuals NA Illumina [426070] (imputed) 2 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261405 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at lumbar spine (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90261406 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right total hip (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261407 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left total hip (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261408 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right femoral neck (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261409 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left femoral neck (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 1 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261410 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right trochanter (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261411 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left trochanter (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261412 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right intertrochanter (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261413 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left intertrochanter (model 2) 2,364 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 trochanter bone mineral density http://www.ebi.ac.uk/efo/EFO_0020095 GCST90261414 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at lumbar spine (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 spine bone mineral density http://www.ebi.ac.uk/efo/EFO_0007701 GCST90261415 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right total hip (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261416 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left total hip (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 hip bone mineral density http://www.ebi.ac.uk/efo/EFO_0007702 GCST90261417 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at right femoral neck (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261418 Genome-wide genotyping array 2023-05-11 36228083 Zeng H 2022-10-13 J Clin Endocrinol Metab www.ncbi.nlm.nih.gov/pubmed/36228083 Twelve loci associated with bone density in middle-aged and elderly Chinese: the Shanghai Changfeng Study. Bone mineral density at left femoral neck (model 2) 3,064 Chinese ancestry individuals NA Illumina [426070] (imputed) 0 femoral neck bone mineral density http://www.ebi.ac.uk/efo/EFO_0007785 GCST90261419 Genome-wide genotyping array 2023-03-09 36566681 Haghighatfard A 2022-12-23 Res Dev Disabil www.ncbi.nlm.nih.gov/pubmed/36566681 The first genome-wide association study of internet addiction; Revealed substantial shared risk factors with neurodevelopmental psychiatric disorders. Internet addiction disorder 16,520 Persian, Kurdish, Arab or Armenian ancestry cases, 18,000 Persian, Kurdish, Arab or Armenian ancestry controls NA NR [183649] 29 internet addiction disorder http://www.ebi.ac.uk/efo/EFO_0803368 GCST90255366 Genome-wide genotyping array 2023-04-03 36519390 Burns AC 2022-12-15 Sleep www.ncbi.nlm.nih.gov/pubmed/36519390 Genome-wide gene by environment study of time spent in daylight and chronotype identifies emerging genetic architecture underlying light sensitivity. Chronotype x daytime light exposure interaction 280,897 British ancestry individuals NA Affymetrix [14055103] (imputed) 3 chronotype measurement, sun exposure measurement http://www.ebi.ac.uk/efo/EFO_0008328, http://www.ebi.ac.uk/efo/EFO_0010729 GCST90267308 Genome-wide genotyping array 2023-04-03 36519390 Burns AC 2022-12-15 Sleep www.ncbi.nlm.nih.gov/pubmed/36519390 Genome-wide gene by environment study of time spent in daylight and chronotype identifies emerging genetic architecture underlying light sensitivity. Chronotype in low daytime light exposure 121,922 European ancestry individuals NA Affymetrix [NR] (imputed) 1 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90267309 Genome-wide genotyping array 2023-04-03 36519390 Burns AC 2022-12-15 Sleep www.ncbi.nlm.nih.gov/pubmed/36519390 Genome-wide gene by environment study of time spent in daylight and chronotype identifies emerging genetic architecture underlying light sensitivity. Chronotype in high daytime light exposure 118,429 European ancestry individuals NA Affymetrix [NR] (imputed) 1 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90267310 Genome-wide genotyping array 2023-04-14 36699085 Hurkmans EGE 2023-01-09 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36699085 Genome-wide analyses of platinum-induced ototoxicity in childhood cancer patients: Results of GO-CAT and United Kingdom MAGIC consortia. Platinum-induced ototoxicity in childhood cancer 302 European ancestry cases, 207 European ancestry controls 168 European ancestry cases, 222 European ancestry controls Illumina [7272049] (imputed) 1 ototoxicity, response to platinum based chemotherapy http://www.ebi.ac.uk/efo/EFO_0006951, http://www.ebi.ac.uk/efo/EFO_0004647 GCST90267543 Genome-wide genotyping array 2023-03-10 36774100 Weston E 2022-11-01 J Nutr www.ncbi.nlm.nih.gov/pubmed/36774100 Investigating Genetic Determinants of Plasma Inositol Status in Adult Humans. Plasma myo-inositol levels 2,232 individuals NA Illumina [757577] 8 Myoinositol measurement http://www.ebi.ac.uk/efo/EFO_0021652 GCST90255680 Genome-wide genotyping array 2023-05-19 36769754 Li C 2023-01-31 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36769754 The Causal Association of Irritable Bowel Syndrome with Multiple Disease Outcomes: A Phenome-Wide Mendelian Randomization Study. Irritable bowel syndrome 20,027 British ancestry cases, 153,149 British ancestry controls NA Affymetrix [6279351] (imputed) 0 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90269915 Genome-wide genotyping array 2023-04-03 36510703 Jo J 2022-12-12 Genes Brain Behav www.ncbi.nlm.nih.gov/pubmed/36510703 Genome-wide assessment reveals a significant association between ACSS3 and physical activity. Physical activity 8,252 East Asian ancestry individuals 172,435 European ancestry cases, 144,515 European ancestry controls Affymetrix [2915187] (imputed) 1 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90267027 Genome-wide genotyping array 2023-02-16 36324647 Watson HJ 2021-09-20 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324647 Common Genetic Variation and Age of Onset of Anorexia Nervosa. Anorexia nervosa (age of onset) 9,335 European ancestry individuals NA NR [NR] (imputed) 1 age of onset of anorexia nervosa http://purl.obolibrary.org/obo/OBA_2050099 GCST90239645 Genome-wide genotyping array 2023-02-16 36324647 Watson HJ 2021-09-20 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324647 Common Genetic Variation and Age of Onset of Anorexia Nervosa. Early-onset anorexia nervosa 1,269 European ancestry cases, 25,042 European ancestry controls NA NR [NR] (imputed) 4 age of onset of anorexia nervosa http://purl.obolibrary.org/obo/OBA_2050099 GCST90239646 Genome-wide genotyping array 2023-02-16 36324647 Watson HJ 2021-09-20 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324647 Common Genetic Variation and Age of Onset of Anorexia Nervosa. Typical-onset anorexia nervosa 6,998 European ancestry cases, 25,042 European ancestry controls NA NR [NR] (imputed) 6 anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0005351 GCST90239647 Genome-wide genotyping array 2023-02-28 36762574 Yao M 2023-02-10 J Med Virol www.ncbi.nlm.nih.gov/pubmed/36762574 Disentangling the common genetic architecture and causality of rheumatoid arthritis and systemic lupus erythematosus with COVID-19 outcomes: genome-wide cross trait analysis and bi-directional Mendelian randomization study. Severe COVID-19 or rheumatoid arthritis (MTAG) 13,769 European ancestry severe COVID-19 cases, 14,361 European ancestry RA cases, 1,116,365 European ancestry controls NA NR [NR] 23 rheumatoid arthritis, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000685, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255367 Genome-wide genotyping array 2023-02-28 36762574 Yao M 2023-02-10 J Med Virol www.ncbi.nlm.nih.gov/pubmed/36762574 Disentangling the common genetic architecture and causality of rheumatoid arthritis and systemic lupus erythematosus with COVID-19 outcomes: genome-wide cross trait analysis and bi-directional Mendelian randomization study. COVID-19 hospitalization or rheumatoid arthritis (MTAG) 32,519 European ancestry COVID-19 hospitalization cases, 14,361 European ancestry RA cases, 2,106,728 European ancestry controls NA NR [NR] 28 rheumatoid arthritis, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000685, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255368 Genome-wide genotyping array 2023-02-28 36762574 Yao M 2023-02-10 J Med Virol www.ncbi.nlm.nih.gov/pubmed/36762574 Disentangling the common genetic architecture and causality of rheumatoid arthritis and systemic lupus erythematosus with COVID-19 outcomes: genome-wide cross trait analysis and bi-directional Mendelian randomization study. COVID-19 infection or rheumatoid arthritis (MTAG) 122,616 European ancestry COVID-19 infection cases, 14,361 European ancestry RA cases, 2,519,163 European ancestry controls NA NR [NR] 10 rheumatoid arthritis, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000685, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255369 Genome-wide genotyping array 2023-02-28 36762574 Yao M 2023-02-10 J Med Virol www.ncbi.nlm.nih.gov/pubmed/36762574 Disentangling the common genetic architecture and causality of rheumatoid arthritis and systemic lupus erythematosus with COVID-19 outcomes: genome-wide cross trait analysis and bi-directional Mendelian randomization study. Severe COVID-19 or systemic lupus erythematosus (MTAG) 13,769 European ancestry severe COVID-19 cases, 7,219 European ancestry SLE cases, 1,088,433 European ancestry controls NA NR [NR] 14 systemic lupus erythematosus, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007915, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255370 Genome-wide genotyping array 2023-02-28 36762574 Yao M 2023-02-10 J Med Virol www.ncbi.nlm.nih.gov/pubmed/36762574 Disentangling the common genetic architecture and causality of rheumatoid arthritis and systemic lupus erythematosus with COVID-19 outcomes: genome-wide cross trait analysis and bi-directional Mendelian randomization study. COVID-19 hospitalization or systemic lupus erythematosus (MTAG) 32,519 European ancestry COVID-19 hospitalization cases, 7,219 European ancestry SLE cases, 2,078,796 European ancestry controls NA NR [NR] 17 systemic lupus erythematosus, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007915, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255371 Genome-wide genotyping array 2023-02-28 36762574 Yao M 2023-02-10 J Med Virol www.ncbi.nlm.nih.gov/pubmed/36762574 Disentangling the common genetic architecture and causality of rheumatoid arthritis and systemic lupus erythematosus with COVID-19 outcomes: genome-wide cross trait analysis and bi-directional Mendelian randomization study. COVID-19 infection or systemic lupus erythematosus (MTAG) 122,616 European ancestry COVID-19 infection cases, 7,219 European ancestry SLE cases, 2,491,231 European ancestry controls NA NR [NR] 7 systemic lupus erythematosus, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007915, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90255372 Genome-wide genotyping array 2023-11-07 37872160 Williams AT 2023-10-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37872160 Genome-wide association study of thyroid-stimulating hormone highlights new genes, pathways and associations with thyroid disease. Thyroid stimulating hormone levels 247,107 European ancestry individuals 63,326 European ancestry individuals, 33,171 South Asian ancestry individuals Affymetrix, Illumina [57524162] (imputed) 245 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST90296333 Genome-wide genotyping array 2023-05-11 36848389 Currant H 2023-02-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36848389 Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation. Outer nuclear layer (ONL) thickness 31,135 European ancestry individuals NA NR [9745601] (imputed) 0 outer nuclear layer thickness measurement http://www.ebi.ac.uk/efo/EFO_0803371 GCST90243953 Genome-wide genotyping array 2023-05-11 36848389 Currant H 2023-02-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36848389 Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation. Inner segment (IS) thickness 31,135 European ancestry individuals NA NR [9745601] (imputed) 0 inner segment thickness measurement http://www.ebi.ac.uk/efo/EFO_0803372 GCST90243954 Genome-wide genotyping array 2023-05-11 36848389 Currant H 2023-02-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36848389 Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation. Outer segment (OS) thickness 31,135 European ancestry individuals NA NR [9745601] (imputed) 0 outer segment thickness measurement http://www.ebi.ac.uk/efo/EFO_0803373 GCST90243955 Genome-wide genotyping array 2023-05-11 36848389 Currant H 2023-02-27 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/36848389 Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation. Photoreceptor cell layer thickness phenotypes (MTAG) 31,135 European ancestry individuals NA NR [9745601] (imputed) 111 photoreceptor cell layer thickness measurement http://www.ebi.ac.uk/efo/EFO_0803370 GCST90255614 Genome-wide genotyping array 2023-06-01 35793981 Kim B 2022-07-06 J Atheroscler Thromb www.ncbi.nlm.nih.gov/pubmed/35793981 Genetic Variants Associated with Supernormal Coronary Arteries. Supernormal coronary arteries 72 Korean ancestry supernormal male cases, 94 Korean ancestry coronary artery disease male controls NA NR [5197138] (imputed) 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90270122 Genome-wide genotyping array 2023-06-07 36996817 Vukadinovic M 2023-03-09 Med www.ncbi.nlm.nih.gov/pubmed/36996817 Deep learning-enabled analysis of medical images identifies cardiac sphericity as an early marker of cardiomyopathy and related outcomes. Left ventricle sphericity index 22,528 European ancestry individuals NA NR [9278050] (imputed) 4 left ventricle sphericity index http://www.ebi.ac.uk/efo/EFO_0020938 GCST90268402 Genome-wide genotyping array 2023-06-07 36996817 Vukadinovic M 2023-03-09 Med www.ncbi.nlm.nih.gov/pubmed/36996817 Deep learning-enabled analysis of medical images identifies cardiac sphericity as an early marker of cardiomyopathy and related outcomes. Left ventricle short axis 22,528 European ancestry individuals NA NR [NR] (imputed) 3 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90269910 Genome-wide genotyping array 2023-06-07 36996817 Vukadinovic M 2023-03-09 Med www.ncbi.nlm.nih.gov/pubmed/36996817 Deep learning-enabled analysis of medical images identifies cardiac sphericity as an early marker of cardiomyopathy and related outcomes. Left ventricle long axis 22,528 European ancestry individuals NA NR [NR] (imputed) 2 left ventricular structural measurement http://www.ebi.ac.uk/efo/EFO_0008205 GCST90269911 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Alcohol frequency weekly (weighted GWA) 102,020 European ancestry individuals NA NR [7296933] (imputed) 4 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90267267 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. BMI (standard GWA) 283,749 European ancestry individuals NA NR [7296935] (imputed) 258 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90267268 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. BMI (weighted GWA) 102,215 European ancestry individuals NA NR [7296935] (imputed) 32 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90267269 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Cancer (standard GWA) 283,034 European ancestry individuals NA NR [7296889] (imputed) 5 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90267270 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Cancer (weighted GWA) 101,903 European ancestry individuals NA NR [7296889] (imputed) 2 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90267271 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. LDL (standard GWA) 269,545 European ancestry individuals NA NR [7296877] (imputed) 149 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90267272 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. LDL (weighted GWA) 97,011 European ancestry individuals NA NR [7296877] (imputed) 48 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90267273 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Coffee intake (standard GWA) 263,464 European ancestry individuals NA NR [7296975] (imputed) 24 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90267274 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Coffee intake (weighted GWA) 94,643 European ancestry individuals NA NR [7296975] (imputed) 4 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90267275 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Depression/anxiety (standard GWA) 282,802 European ancestry individuals NA NR [7296966] (imputed) 3 unipolar depression, anxiety http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90267276 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Depression/anxiety (weighted GWA) 101,859 European ancestry individuals NA NR [7296966] (imputed) 3 unipolar depression, anxiety http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0005230 GCST90267277 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Diabetes (standard GWA) 283,227 European ancestry individuals NA NR [7296942] (imputed) 40 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90267278 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Diabetes (weighted GWA) 102,023 European ancestry individuals NA NR [7296942] (imputed) 4 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90267279 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Age when finished full-time education (standard GWA) 283,749 European ancestry individuals NA NR [7296935] (imputed) 245 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST90267280 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Age when finished full-time education (weighted GWA) 102,215 European ancestry individuals NA NR [7296935] (imputed) 51 self reported educational attainment http://www.ebi.ac.uk/efo/EFO_0004784 GCST90267281 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Fruit intake (standard GWA) 273,875 European ancestry individuals NA NR [7297015] (imputed) 16 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90267282 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Fruit intake (weighted GWA) 98,925 European ancestry individuals NA NR [7297015] (imputed) 1 diet measurement http://www.ebi.ac.uk/efo/EFO_0008111 GCST90267283 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Height (standard GWA) 283,749 European ancestry individuals NA NR [7296935] (imputed) 671 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90267284 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Height (weighted GWA) 102,215 European ancestry individuals NA NR [7296935] (imputed) 161 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90267285 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Insomnia (standard GWA) 283,595 European ancestry individuals NA NR [7296914] (imputed) 18 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90267286 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Insomnia (weighted GWA) 102,156 European ancestry individuals NA NR [7296914] (imputed) 1 insomnia http://www.ebi.ac.uk/efo/EFO_0004698 GCST90267287 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Loneliness (standard GWA) 279,941 European ancestry individuals NA NR [7296886] (imputed) 3 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST90267288 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Loneliness (weighted GWA) 100,928 European ancestry individuals NA NR [7296886] (imputed) 1 loneliness measurement http://www.ebi.ac.uk/efo/EFO_0007865 GCST90267289 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Number of non-cancer illnesses (standard GWA) 283,743 European ancestry individuals NA NR [7296943] (imputed) 15 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90267290 Genome-wide genotyping array 2023-05-11 37106081 Schoeler T 2023-04-27 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37106081 Participation bias in the UK Biobank distorts genetic associations and downstream analyses. Number of non-cancer illnesses (weighted GWA) 102,213 European ancestry individuals NA NR [7296943] (imputed) 2 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90267291 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-palmitoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-palmitoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021089 GCST90128995 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-stearoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-stearoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021098 GCST90128996 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-docosahexaenoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-docosahexaenoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021079 GCST90128997 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-arachidonoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-arachidonoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021076 GCST90128998 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-docosahexaenoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-docosahexaenoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021079 GCST90128999 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Butyrylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 butyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020010 GCST90129000 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Carnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90129001 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Decanoylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90129002 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Acetylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90129003 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Propionylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90129004 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Isovalerylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 isovalerylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020019 GCST90129005 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hexanoylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90129006 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Octanoylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90129007 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glutamine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90129008 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glycine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90129009 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glucose levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90129010 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Histidine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90129011 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Ornithine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90129012 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Tryptophan levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90129013 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-eicosatrienoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-eicosatrienoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021081 GCST90129014 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-heptadecanoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-heptadecanoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021082 GCST90129015 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Tyrosine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90129016 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Laurylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90129017 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Threonine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90129018 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Methionine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90129019 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103604 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103605 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103606 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103607 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103608 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103609 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 5 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103610 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103611 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103612 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103613 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103614 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103615 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103616 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103617 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103618 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103619 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103620 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103621 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103622 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103623 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103624 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103625 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103626 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103627 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103628 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phenylalanine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90129020 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Arginine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90129021 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Serine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90129022 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-tetradecenoyl carnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90129023 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Oleoylcarnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90129024 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-linoleoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-linoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021083 GCST90129025 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glutaroyl carnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glutaroyl carnitine measurement http://www.ebi.ac.uk/efo/EFO_0021005 GCST90129026 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-myristoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-myristoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021085 GCST90129027 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hydroxyisovaleroyl carnitine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90129028 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-oleoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-oleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021086 GCST90129029 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103629 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103630 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (24 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103631 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in breast cancer 2,801 European ancestry individuals NA Illumina [NR] (imputed) 0 overall survival, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90104804 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in breast cancer 2,801 European ancestry individuals, 450 East Asian ancestry individuals, 392 Hispanic or Latin American individuals, 330 African American or Afro-Caribbean individuals NA Illumina [NR] (imputed) 1 overall survival, breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0000305 GCST90104805 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in breast cancer treated with Par-4 dependent chemotherapy 949 European ancestry individuals NA Illumina [NR] (imputed) 1 overall survival, response to Par-4 dependent chemotherapy http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0021535 GCST90104806 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in breast cancer treated with Par-4 dependent chemotherapy 949 European ancestry individuals, 195 East Asian ancestry individuals, 168 Hispanic or Latin American individuals, 149 African American or Afro-Caribbean individuals 609 European ancestry individuals, 2,750 East Asian ancestry individuals Illumina [NR] (imputed) 1 overall survival, response to Par-4 dependent chemotherapy http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_0021535 GCST90104807 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in breast cancer treated with chemotherapy (excluding Par-4 dependent chemotherapy) 1,852 European ancestry individuals NA Illumina [NR] (imputed) 2 overall survival, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0000638, http://purl.obolibrary.org/obo/GO_0097327 GCST90104808 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in breast cancer treated with chemotherapy (excluding Par-4 dependent chemotherapy) 1,852 European ancestry individuals, 255 East Asian ancestry individuals, 224 Hispanic or Latin American individuals, 181 African American or Afro-Caribbean individuals NA Illumina [NR] (imputed) 2 overall survival, response to antineoplastic agent http://www.ebi.ac.uk/efo/EFO_0000638, http://purl.obolibrary.org/obo/GO_0097327 GCST90104809 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in ER positive breast cancer 2,407 European ancestry individuals NA Illumina [NR] (imputed) 1 overall survival, estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1000649 GCST90104810 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in ER positive breast cancer 2,407 European ancestry individuals, 374 East Asian ancestry individuals, 325 Hispanic or Latin American individuals, 220 African American or Afro-Caribbean individuals NA Illumina [NR] (imputed) 0 overall survival, estrogen-receptor positive breast cancer http://www.ebi.ac.uk/efo/EFO_0000638, http://www.ebi.ac.uk/efo/EFO_1000649 GCST90104811 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in ER negative breast cancer 393 European ancestry individuals NA Illumina [NR] (imputed) 1 estrogen-receptor negative breast cancer, overall survival http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90104812 Genome-wide genotyping array 2022-07-20 35322040 Zhu Q 2022-03-23 NPJ Breast Cancer www.ncbi.nlm.nih.gov/pubmed/35322040 UACA locus is associated with breast cancer chemoresistance and survival. Overall survival in ER negative breast cancer 393 European ancestry individuals, 76 East Asian ancestry individuals, 67 Hispanic or Latin American individuals, 109 African American or Afro-Caribbean individuals NA Illumina [NR] (imputed) 0 estrogen-receptor negative breast cancer, overall survival http://www.ebi.ac.uk/efo/EFO_1000650, http://www.ebi.ac.uk/efo/EFO_0000638 GCST90104813 Genome-wide genotyping array 2022-08-04 35484098 Zhao M 2022-04-28 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35484098 Different responses to risperidone treatment in Schizophrenia: a multicenter genome-wide association and whole exome sequencing joint study. Response to risperidone in schizophrenia 189 Han Chinese ancestry cases NA Illumina [446504] (imputed) 7 response to risperidone http://purl.obolibrary.org/obo/GO_0097336 GCST90131475 Genome-wide genotyping array 2022-08-04 35484098 Zhao M 2022-04-28 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/35484098 Different responses to risperidone treatment in Schizophrenia: a multicenter genome-wide association and whole exome sequencing joint study. Response to risperidone in schizophrenia 222 Han Chinese ancestry cases NA Illumina [108813] 3 response to risperidone http://purl.obolibrary.org/obo/GO_0097336 GCST90131476 Exome-wide sequencing 2022-07-25 34077760 Alipanahi B 2021-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34077760 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology. Vertical cup-disc ratio 65,680 European ancestry individuals NA Affymetrix [13110443] (imputed) 299 cup-to-disc ratio measurement http://www.ebi.ac.uk/efo/EFO_0006939 GCST90129592 Genome-wide genotyping array 2022-07-25 34077760 Alipanahi B 2021-06-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/34077760 Large-scale machine-learning-based phenotyping significantly improves genomic discovery for optic nerve head morphology. Vertical cup-disc ratio 89,579 European ancestry individuals NA Affymetrix [8600000] (imputed) 375 cup-to-disc ratio measurement http://www.ebi.ac.uk/efo/EFO_0006939 GCST90129627 Genome-wide genotyping array 2022-05-18 35074755 Meng Y 2022-01-24 Cancer Res www.ncbi.nlm.nih.gov/pubmed/35074755 Genome-wide association analyses identify CATSPERE as a mediator of colorectal cancer susceptibility and progression. Colorectal cancer 1,955 Han Chinese ancestry cases, 2,272 Han Chinese ancestry controls 5,231 Han Chinese ancestry cases, 6,240 Han Chinese ancestry controls Illumina [4131996] (imputed) 1 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90102510 Genome-wide genotyping array 2022-07-01 35401680 Jung T 2022-03-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/35401680 Integrative Pathway Analysis of SNP and Metabolite Data Using a Hierarchical Structural Component Model. Dimethylglycine levels 627 Korean ancestry individuals NA Affymetrix [312116] 15 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90105033 Genome-wide genotyping array 2022-07-01 35401680 Jung T 2022-03-24 Front Genet www.ncbi.nlm.nih.gov/pubmed/35401680 Integrative Pathway Analysis of SNP and Metabolite Data Using a Hierarchical Structural Component Model. Glycine levels 627 Korean ancestry individuals NA Affymetrix [312116] 17 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90105034 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Red blood cell erythrocyte count (UKB data field 30010) (CNV deletion-only model) 322,500 white British ancestry individuals NA NR [9936] 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90027426 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Reticulocyte count (UKB data field 30250) (CNV deletion-only model) 317,487 white British ancestry individuals NA NR [9936] 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90027427 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Sex hormone binding globulin levels (UKB data field 30830) (CNV deletion-only model) 288,310 white British ancestry individuals NA NR [9936] 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90027428 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Systolic blood pressure automated reading (UKB data field 4080) (CNV deletion-only model) 313,181 white British ancestry individuals NA NR [9936] 0 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90027429 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Testosterone levels (UKB data field 30850) (CNV deletion-only model) 287,926 white British ancestry individuals NA NR [9936] 0 testosterone measurement http://www.ebi.ac.uk/efo/EFO_0004908 GCST90027430 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Triglyceride levels (UKB data field 30870) (CNV deletion-only model) 316,681 white British ancestry individuals NA NR [9936] 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90027431 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Total protein levels (UKB data field 30860) (CNV deletion-only model) 290,746 white British ancestry individuals NA NR [9936] 0 blood protein measurement http://www.ebi.ac.uk/efo/EFO_0007937 GCST90027432 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Urate levels (UKB data field 30880) (CNV deletion-only model) 316,545 white British ancestry individuals NA NR [9936] 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90027433 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Urea levels (UKB data field 30670) (CNV deletion-only model) 316,737 white British ancestry individuals NA NR [9936] 0 serum urea measurement http://www.ebi.ac.uk/efo/EFO_0009795 GCST90027434 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Vitamin D levels (UKB data field 30890) (CNV deletion-only model) 303,212 white British ancestry individuals NA NR [9936] 0 vitamin D measurement http://www.ebi.ac.uk/efo/EFO_0004631 GCST90027435 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. White blood cell leukocyte count (UKB data field 30000) (CNV deletion-only model) 322,497 white British ancestry individuals NA NR [9936] 0 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90027436 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Weight (UKB data field 21002) (CNV deletion-only model) 330,607 white British ancestry individuals NA NR [9936] 0 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90027437 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Waist-hip ratio (UKB data field 49/48) (CNV deletion-only model) 330,926 white British ancestry individuals NA NR [9936] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90027438 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Waist-to-hip ratio adjusted for BMI (UKB data field 49/48) (CNV deletion-only model) 330,414 white British ancestry individuals NA NR [9936] 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90027439 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Balding (UKB data field 2395) (CNV deletion-only model) 152,044 white British ancestry males NA NR [9936] 0 balding measurement http://www.ebi.ac.uk/efo/EFO_0007825 GCST90027440 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Relative age of first facial hair (UKB data field 2375) (CNV deletion-only model) 148,371 white British ancestry males NA NR [9936] 0 age at first facial hair http://www.ebi.ac.uk/efo/EFO_0009716 GCST90027441 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Birth weight of first child (UKB data field 2744) (CNV deletion-only model) 143,630 white British ancestry females NA NR [9936] 0 birth weight http://www.ebi.ac.uk/efo/EFO_0004344 GCST90027442 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Age at menarche (UKB data field 2714) (CNV deletion-only model) 173,725 white British ancestry females NA NR [9936] 0 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90027443 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Age at menopause (UKB data field 3581) (CNV deletion-only model) 105,469 white British ancestry females NA NR [9936] 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90027444 Genome-wide genotyping array 2022-08-04 35729236 Ahmed M 2022-06-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35729236 Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Hormone-sensitive cancer 15,197 White ancestry cases, 223,207 White ancestry controls NA Affymetrix [1217312] (imputed) 12 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90102436 Genome-wide genotyping array 2022-08-04 35729236 Ahmed M 2022-06-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35729236 Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Postmenopausal breast cancer 7,090 White ancestry cases, 223,207 White ancestry controls NA Affymetrix [1217312] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90102437 Genome-wide genotyping array 2022-08-04 35729236 Ahmed M 2022-06-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35729236 Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Ovarian cancer 1,063 White ancestry cases, 223,207 White ancestry controls NA Affymetrix [1217312] (imputed) 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90102438 Genome-wide genotyping array 2022-08-04 35729236 Ahmed M 2022-06-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35729236 Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Prostate cancer 5,643 White ancestry cases, 223,207 White ancestry controls NA Affymetrix [1217312] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90102439 Genome-wide genotyping array 2022-08-04 35729236 Ahmed M 2022-06-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35729236 Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Thyroid cancer 365 White ancestry cases, 223,207 White ancestry controls NA Affymetrix [1217312] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90102440 Genome-wide genotyping array 2022-08-04 35729236 Ahmed M 2022-06-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35729236 Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Uterine cancer 1,036 White ancestry cases, 223,207 White ancestry controls NA Affymetrix [1217312] (imputed) 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90102441 Genome-wide genotyping array 2022-08-04 35729236 Ahmed M 2022-06-21 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35729236 Considering hormone-sensitive cancers as a single disease in the UK biobank reveals shared aetiology. Incident hormone-sensitive cancer 7,038 White ancestry cases, 223,207 White ancestry controls NA Affymetrix [1217312] (imputed) 8 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90102435 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Phosphate levels (UKB data field 30810) (CNV deletion-only model) 290,512 white British ancestry individuals NA NR [9936] 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90027424 Genome-wide genotyping array 2022-04-27 35240056 Auwerx C 2022-03-02 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35240056 The individual and global impact of copy-number variants on complex human traits. Platelet count (UKB data field 30080) (CNV deletion-only model) 322,499 white British ancestry individuals NA NR [9936] 0 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90027425 Genome-wide genotyping array 2022-08-01 35470498 Xia L 2022-04-25 J Clin Lab Anal www.ncbi.nlm.nih.gov/pubmed/35470498 Genome-wide association study of 7661 Chinese Han individuals and fine-mapping major histocompatibility complex identifies HLA-DRB1 as associated with IgA vasculitis. Immunoglobulin A vasculitis 496 Chinese ancestry cases, 7,165 Chinese ancestry controls NA Illumina [377302] (imputed) 2 Henoch-Schoenlein purpura http://www.ebi.ac.uk/efo/EFO_1000965 GCST90131441 Genome-wide genotyping array 2022-08-04 35866869 Gilchrist J 2022-07-22 Elife www.ncbi.nlm.nih.gov/pubmed/35866869 BIRC6 modifies risk of invasive bacterial infection in Kenyan children. Invasive bacterial infection 2,588 Sub-Saharan African ancestry cases, 2,812 Sub-Saharan African ancestry controls NA Affymetrix, Illumina [13999771] (imputed) 1 bacterial disease http://www.ebi.ac.uk/efo/EFO_0000771 GCST90094632 Genome-wide genotyping array 2022-06-17 35298028 Campbell C 2022-03-17 Epilepsia www.ncbi.nlm.nih.gov/pubmed/35298028 A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam. Response to levetiracetam (behavioral disorder) 149 European ancestry cases, 920 European ancestry controls NA Illumina [3800000] (imputed) 0 Atypical behavior, response to anticonvulsant http://purl.obolibrary.org/obo/HP_0000708, http://purl.obolibrary.org/obo/GO_0036277 GCST90104620 Genome-wide genotyping array 2022-06-17 35298028 Campbell C 2022-03-17 Epilepsia www.ncbi.nlm.nih.gov/pubmed/35298028 A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam. Response to levetiracetam (psychotic reaction) 37 European ancestry cases, 920 European ancestry controls NA Illumina [3800000] (imputed) 0 psychotic symptoms, response to anticonvulsant http://www.ebi.ac.uk/efo/EFO_0005940, http://purl.obolibrary.org/obo/GO_0036277 GCST90104621 Genome-wide genotyping array 2022-09-21 36034232 Duarte RRR 2022-08-04 iScience www.ncbi.nlm.nih.gov/pubmed/36034232 Transcriptome-wide association study of HIV-1 acquisition identifies HERC1 as a susceptibility gene. HIV-1 susceptibility 7,303 European ancestry cases, 587,343 European ancestry controls NA NR [5347926] 5 HIV-1 infection http://www.ebi.ac.uk/efo/EFO_0000180 GCST90137495 Genome-wide genotyping array 2022-08-03 35592775 Wang Z 2022-05-03 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35592775 The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. Obesity 451,145 European ancestry individuals NA Affymetrix [NR] (imputed) 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90131480 Genome-wide genotyping array 2022-08-03 35592775 Wang Z 2022-05-03 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35592775 The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. Obesity (extreme) 451,145 European ancestry individuals NA Affymetrix [NR] (imputed) 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90131481 Genome-wide genotyping array 2022-08-03 35592775 Wang Z 2022-05-03 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35592775 The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. Body mass index 184,385 European ancestry individuals NA NR [NR] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90131482 Exome-wide sequencing 2022-08-03 35592775 Wang Z 2022-05-03 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35592775 The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. Obesity 184,385 European ancestry individuals NA NR [NR] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90131483 Exome-wide sequencing 2022-08-03 35592775 Wang Z 2022-05-03 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35592775 The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. Obesity (extreme) 184,385 European ancestry individuals NA NR [NR] 0 obesity http://www.ebi.ac.uk/efo/EFO_0001073 GCST90131484 Exome-wide sequencing 2022-08-03 35592775 Wang Z 2022-05-03 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/35592775 The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. Body mass index 451,145 European ancestry individuals NA Affymetrix [NR] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90131479 Genome-wide genotyping array 2022-08-31 35752658 Yamada H 2022-06-25 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/35752658 A machine learning model using SNPs obtained from a genome-wide association study predicts the onset of vincristine-induced peripheral neuropathy. Vincristine-induced peripheral neuropathy in cancer 36 East Asian ancestry cases with peripheral neuropathy, 20 East Asian ancestry cases without peripheral neuropathy NA Illumina [4340175] (imputed) 0 peripheral neuropathy, response to vincristine http://www.ebi.ac.uk/efo/EFO_0003100, http://www.ebi.ac.uk/efo/EFO_0006950 GCST90134249 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-palmitoleoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-palmitoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021088 GCST90129030 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-palmitoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-palmitoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021089 GCST90129031 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-stearoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-stearoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021092 GCST90129032 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-linoleoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-linoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021095 GCST90129033 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-palmitoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-palmitoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021097 GCST90129037 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-stearoylglycerophosphocholine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-stearoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021098 GCST90129038 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Proline levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90129039 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Valine levels (Biocrates platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90129040 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-linoleoylglycerophosphoethanolamine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-linoleoylglycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0021084 GCST90128857 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-methylurate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90128858 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-methylxanthine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90128859 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-palmitoylglycerophosphoinositol levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-palmitoylglycerophosphoinositol measurement http://www.ebi.ac.uk/efo/EFO_0021091 GCST90128860 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-stearoylglycerol (1-monostearin) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 2 1-stearoylglycerol 1-monostearin measurement http://www.ebi.ac.uk/efo/EFO_0021111 GCST90128861 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-stearoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-stearoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021092 GCST90128862 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1,3,7-trimethylurate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90128863 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 10-undecenoate (11:1n1) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90128864 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-aminobutyrate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90128865 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 3-(cystein-S-yl)acetaminophen levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 3-cystein-S-ylacetaminophen measurement http://www.ebi.ac.uk/efo/EFO_0021155 GCST90128866 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 4-acetamidobutanoate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90128867 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 5-oxoproline levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90128868 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Androsterone sulfate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90128869 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Xleu levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90128970 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Proline levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90128971 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Valine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90128972 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Tyrosine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90128973 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Laurylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90128974 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Threonine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90128975 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Methionine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90128976 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phenylalanine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90128977 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Arginine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90128978 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Serine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90128979 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-tetradecenoyl carnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90128980 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Oleoylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90128981 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-palmitoleoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-palmitoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021088 GCST90128982 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Glutaroyl carnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 glutaroyl carnitine measurement http://www.ebi.ac.uk/efo/EFO_0021005 GCST90128983 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-myristoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-myristoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021085 GCST90128984 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hydroxyisovaleroyl carnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90128985 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-linoleoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-linoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021095 GCST90128986 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-linoleoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-linoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021083 GCST90128987 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-eicosatrienoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-eicosatrienoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021081 GCST90128988 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-oleoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-oleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021086 GCST90128989 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-oleoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-oleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021096 GCST90128990 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Palmitoylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90128991 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Stearoylcarnitine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90128992 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 1-heptadecanoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 1-heptadecanoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021082 GCST90128993 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. 2-palmitoylglycerophosphocholine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 2-palmitoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021097 GCST90128994 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103529 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103530 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103531 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103532 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 5 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103533 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103534 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103535 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103536 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103537 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103538 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103539 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103540 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103541 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103542 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 6 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103543 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103544 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103545 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 4 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103546 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103547 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103548 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103549 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103550 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (12 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103551 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103552 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103553 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103504 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 5 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103505 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103506 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 4 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103507 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 6 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103508 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103509 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103510 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103511 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103512 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103513 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103514 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103515 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103516 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 4 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103517 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103518 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (baseline) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103519 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103520 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103521 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103522 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 4 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103523 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103524 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103525 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103526 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103527 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (6 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103528 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103554 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103555 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103556 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103557 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103558 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103559 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103560 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103561 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103562 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103563 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103564 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103565 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103566 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (24 month visit) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103567 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103568 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103569 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103570 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103571 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103572 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103573 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103574 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103575 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103576 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103577 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103578 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103579 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103580 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103581 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103582 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (baseline)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103583 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103584 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103585 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103586 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103587 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Functional activities questionnaire (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103588 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fluorodeoxyglucose (PET imaging) (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103589 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Amyloid (PET imaging) (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103590 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid amyloid beta 42 levels (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 amyloid-beta measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005194, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103591 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid t-tau levels (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement, t-tau measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0004760 GCST90103592 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Cerebrospinal fluid p-tau levels (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 p-tau measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0004763, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103593 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Whole-brain volume (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 whole-brain volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005089, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103594 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Entorhinal cortical volume (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 entorhinal cortical volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005092, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103595 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Total ventricular volume (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 total ventricular volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0007602, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103596 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Middle temporal gyrus volume (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 3 middle temporal gyrus volume measurement, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0010316, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103597 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Fusiform volume (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement, brain volume measurement http://www.ebi.ac.uk/efo/EFO_0006514, http://www.ebi.ac.uk/efo/EFO_0006930 GCST90103598 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Hippocampal volume (6 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 hippocampal volume, Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0005035, http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103599 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Alzheimer's disease assessment scale (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103600 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Global cognition (Clinical Dementia Rating Scale Sum of Boxes) (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 1 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103601 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Rey auditory verbal learning test (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 0 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103602 Genome-wide genotyping array 2022-05-18 35086473 Lee B 2022-01-28 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/35086473 Genome-Wide association study of quantitative biomarkers identifies a novel locus for alzheimer's disease at 12p12.1. Mini-mental state examination / Folstein test (12 month visit)(adjusted for APOE e4 dosage) 1,576 European ancestry individuals NA Illumina [565373] (imputed) 2 Alzheimer's disease biomarker measurement http://www.ebi.ac.uk/efo/EFO_0006514 GCST90103603 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11421 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 GCST90128945 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11440 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11440 measurement http://www.ebi.ac.uk/efo/EFO_0021234 GCST90128946 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11469 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11469 measurement http://www.ebi.ac.uk/efo/EFO_0021240 GCST90128947 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11529 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11529 measurement http://www.ebi.ac.uk/efo/EFO_0021248 GCST90128948 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11530 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11530 measurement http://www.ebi.ac.uk/efo/EFO_0021249 GCST90128949 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11538 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11538 measurement http://www.ebi.ac.uk/efo/EFO_0021251 GCST90128950 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11593 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11593 measurement http://www.ebi.ac.uk/efo/EFO_0020015 GCST90128951 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11787 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90128952 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11792 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11792 measurement http://www.ebi.ac.uk/efo/EFO_0021259 GCST90128953 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11793 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11793--oxidized bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0021260 GCST90128954 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11818 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-11818 measurement http://www.ebi.ac.uk/efo/EFO_0021264 GCST90128955 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-12063 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-12063 measurement http://www.ebi.ac.uk/efo/EFO_0021283 GCST90128956 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-12092 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-12092 measurement http://www.ebi.ac.uk/efo/EFO_0021284 GCST90128957 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-12093 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-12093 measurement http://www.ebi.ac.uk/efo/EFO_0021285 GCST90128958 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-12435 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-12435 measurement http://www.ebi.ac.uk/efo/EFO_0021306 GCST90128959 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-12510 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-12510--2-aminooctanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0021313 GCST90128960 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-12798 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90128961 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-12844 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90128962 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-13215 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-13215 measurement http://www.ebi.ac.uk/efo/EFO_0021347 GCST90128963 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-13429 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-13429 measurement http://www.ebi.ac.uk/efo/EFO_0021348 GCST90128964 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-13431 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-13431--nonanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021349 GCST90128965 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-13435 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-13435 measurement http://www.ebi.ac.uk/efo/EFO_0021350 GCST90128966 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-14086 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-14086 measurement http://www.ebi.ac.uk/efo/EFO_0021363 GCST90128967 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-14208 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-14208--phenylalanylserine measurement http://www.ebi.ac.uk/efo/EFO_0021366 GCST90128968 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-14632 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-14632 measurement http://www.ebi.ac.uk/efo/EFO_0021375 GCST90128969 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C40:6 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128920 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C42:5 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128921 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C44:5 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128922 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C44:6 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128923 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hydroxysphingomyeline C14:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128924 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hydroxysphingomyeline C16:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128925 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hydroxysphingomyeline C22:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128926 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hydroxysphingomyeline C22:2 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128927 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Hydroxysphingomyeline C24:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128928 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Sphingomyeline C16:0 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128929 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Sphingomyeline C16:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128930 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Sphingomyeline C18:0 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128931 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Sphingomyeline C18:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128932 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Sphingomyeline C24:0 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128933 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Sphingomyeline C24:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90128934 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Succinylcarnitine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90128935 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Thymol sulfate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90128936 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Tryptophan levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90128937 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Urate levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90128938 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-02249 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-02249 measurement http://www.ebi.ac.uk/efo/EFO_0021182 GCST90128939 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-04498 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-04498 measurement http://www.ebi.ac.uk/efo/EFO_0021192 GCST90128940 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-08988 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-08988 measurement http://www.ebi.ac.uk/efo/EFO_0021207 GCST90128941 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-10510 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 X-10510 measurement http://www.ebi.ac.uk/efo/EFO_0021217 GCST90128942 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11244 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 GCST90128943 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. X-11255 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 GCST90128944 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Isobutyrylcarnitine (c4) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90128895 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Laurate (12:0) levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90128896 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Mannose levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90128897 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. N-(2-furoyl)glycine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 N-2-furoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021165 GCST90128898 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. N-acetylornithine levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 GCST90128899 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Ornithine levels (Metabolon platform) 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90128900 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C28:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128901 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C34:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128902 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C34:2 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128903 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C36:2 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128904 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C36:4 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128905 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C36:5 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128906 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C38:3 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128907 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C38:4 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128908 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C38:5 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128909 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine diacyl C40:4 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128910 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C34:1 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128911 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C34:2 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128912 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C36:2 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128913 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C36:3 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128914 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C36:5 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128915 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C38:4 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128916 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C38:5 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128917 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C38:6 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128918 Genome-wide genotyping array 2022-07-18 27073872 Yet I 2016-04-13 PLoS One www.ncbi.nlm.nih.gov/pubmed/27073872 Genetic Influences on Metabolite Levels: A Comparison across Metabolomic Platforms. Phosphatidylcholine acyl-alkyl C40:5 levels 79 monozygotic twin pairs, 215 dizygotic twin pairs, 413 individuals NA Illumina [NR] (imputed) 1 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90128919 Genome-wide genotyping array 2022-07-11 35389749 Nauffal V 2022-04-07 Circulation www.ncbi.nlm.nih.gov/pubmed/35389749 Monogenic and Polygenic Contributions to QTc Prolongation in the Population. QTc interval 79,167 European ancestry individuals, 1,614 African ancestry individuals, 78 Hispanic or Latin American individuals, 1,500 Asian ancestry individuals, 2,271 individuals 16,074 European ancestry individuals, 4,887 African ancestry individuals, 596 Hispanic or Latin American individuals, 768 Asian ancestry individuals, 998 Amish individuals, 3,653 individuals Affymetrix [8595785] (imputed) 35 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90128423 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Bolognese liking 158,113 European ancestry individuals NA Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094710 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Broad bean liking 158,921 European ancestry individuals NA Affymetrix [11353280] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094711 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Broccoli liking 159,414 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094712 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Brown rice liking 156,802 European ancestry individuals NA Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094713 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Brussel sprout liking 159,493 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094714 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Burger liking 158,435 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094715 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-burn/spicy liking (derived food-liking factor) 154,046 European ancestry individuals NA Affymetrix [11353280] (imputed) 13 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094716 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Adding butter to bread liking 159,364 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094717 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Butternut squash liking 148,949 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094718 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cabbage liking 159,516 European ancestry individuals NA Affymetrix [11353280] (imputed) 6 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094719 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-caffeinated/sweet liking (derived food-liking factor) 155,986 European ancestry individuals NA Affymetrix [9604824] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094720 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cake liking 159,518 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094721 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-cake/biscuits liking (derived food-liking factor) 159,522 European ancestry individuals NA Affymetrix [9609947] (imputed) 16 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094722 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cake icing liking 159,470 European ancestry individuals NA Affymetrix [11353280] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094723 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Capers liking 140,886 European ancestry individuals NA Affymetrix [11353280] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094724 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-carbohydrate liking (derived food-liking factor) 159,523 European ancestry individuals NA Affymetrix [9614426] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094725 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-capsicum liking (derived food-liking factor) 157,390 European ancestry individuals NA Affymetrix [9610068] (imputed) 16 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094726 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cauliflower liking 159,496 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094727 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cereal bar liking 155,024 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094728 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-cheese liking (derived food-liking factor) 156,734 European ancestry individuals NA Affymetrix [9609993] (imputed) 13 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094729 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cheesecake liking 159,246 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094730 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cherry liking 159,373 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094731 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Chicken liking 158,559 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094732 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Chilli pepper liking 157,484 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094733 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Chips liking 159,574 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094734 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-chocolate/coffee liking (derived food-liking factor) 158,905 European ancestry individuals NA Affymetrix [9614050] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094735 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cod liking 158,795 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094736 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-coffee/alcohol liking (derived food-liking factor) 158,095 European ancestry individuals NA Affymetrix [9586905] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094737 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Coffee difference liking 157,453 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094738 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Coffee max liking 159,006 European ancestry individuals NA Affymetrix [11353280] (imputed) 6 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094739 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Coffee with sugar liking 158,219 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094740 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Coffee without sugar liking 158,240 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094741 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-cooking flavour liking (derived food-liking factor) 153,323 European ancestry individuals NA Affymetrix [9609729] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094742 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-cooking vegetables liking (derived food-liking factor) 158,645 European ancestry individuals NA Affymetrix [9605623] (imputed) 13 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094743 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Coriander liking 154,301 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094744 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Corn flake liking 159,353 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094745 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cream liking 159,441 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094746 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Crisps liking 159,554 European ancestry individuals NA Affymetrix [11353280] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094747 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Croissant liking 158,623 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094748 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Cucumber liking 159,501 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094749 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Curry liking 159,259 European ancestry individuals NA Affymetrix [11353280] (imputed) 7 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094750 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-dairy liking (derived food-liking factor) 159,365 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094751 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Dark chocolate liking 159,469 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094752 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-deep fried food liking (derived food-liking factor) 158,793 European ancestry individuals NA Affymetrix [9609548] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094753 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-dessert liking (derived food-liking factor) 159,398 European ancestry individuals NA Affymetrix [9569208] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094754 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Diet fizzy drinks liking 157,017 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094755 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Dried fruit liking 159,258 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094756 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Eggs liking 159,447 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094757 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Extra virgin olive oil liking 157,343 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094758 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-fatty/salty food liking (derived food-liking factor) 156,621 European ancestry individuals NA Affymetrix [9596713] (imputed) 15 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094759 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-wine liking (derived food-liking factor) 158,478 European ancestry individuals NA Affymetrix [9618595] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094872 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Whiskey liking 156,904 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094873 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Adding salt to food liking 159,450 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094687 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Alcohol liking 157,286 European ancestry individuals NA Affymetrix [9600548] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094688 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Aniseed liking 152,087 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094689 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Apple juice liking 159,215 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094690 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Apples liking 159,515 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094691 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Asparagus liking 155,886 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094692 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Aubergine liking 152,291 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094693 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Avocado liking 153,095 European ancestry individuals NA Affymetrix [11353280] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094694 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Bacon liking 158,551 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094695 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Baked/steamed fish liking 158,335 European ancestry individuals NA Affymetrix [11353280] (imputed) 7 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094696 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Banana liking 159,469 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094697 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. BBQ/grilled meat liking 158,387 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094698 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Beans liking 159,014 European ancestry individuals NA Affymetrix [9618863] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094699 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Beef/steak liking 158,442 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094700 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Beer liking 156,030 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [9618701] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094701 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Beetroot liking 159,342 European ancestry individuals NA Affymetrix [11353280] (imputed) 4 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094702 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Bell pepper liking 142,261 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094703 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Biscuits liking 159,527 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094704 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Bitter ale liking 155,103 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094705 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-bitter food liking (derived food-liking factor) 157,485 European ancestry individuals NA Affymetrix [11353280] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094706 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Black olive liking 156,251 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094707 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Black pepper liking 158,772 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094708 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Blue cheese liking 157,457 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094709 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-fatty/dairy food liking (derived food-liking factor) 159,335 European ancestry individuals NA Affymetrix [9609311] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094760 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-fatty food liking (derived food-liking factor) 159,481 European ancestry individuals NA Affymetrix [11353280] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094761 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-fish liking (derived food-liking factor) 155,344 European ancestry individuals NA Affymetrix [9578548] (imputed) 25 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094762 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Fizzy drinks liking 158,805 European ancestry individuals NA Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094763 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Fried chicken liking 157,189 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094764 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Fried fish liking 158,855 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094765 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Fruit liking 159,418 European ancestry individuals NA Affymetrix [11353280] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094766 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-fruit liking (derived food-liking factor) 159,218 European ancestry individuals NA Affymetrix [9582267] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094767 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Fruit juice liking 159,344 European ancestry individuals NA Affymetrix [9618730] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094768 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Garlic liking 159,386 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094769 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Gherkins liking 156,020 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094770 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Globe artichoke liking 115,868 European ancestry individuals NA Affymetrix [11353280] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094771 Genome-wide genotyping array 2022-04-27 35421404 Lee SG 2022-04-11 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/35421404 Identification of genetic loci associated with facial wrinkles in a large Korean population. Facial wrinkles (under eye) 11,079 Korean ancestry individuals 5,940 Korean ancestry individuals Illumina [366864] (imputed) 16 skin aging measurement http://www.ebi.ac.uk/efo/EFO_0008006 GCST90094903 Genome-wide genotyping array 2022-04-27 35421404 Lee SG 2022-04-11 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/35421404 Identification of genetic loci associated with facial wrinkles in a large Korean population. Facial wrinkles (crow's feet) 11,079 Korean ancestry individuals 5,940 Korean ancestry individuals Illumina [366864] (imputed) 14 skin aging measurement http://www.ebi.ac.uk/efo/EFO_0008006 GCST90094904 Genome-wide genotyping array 2022-07-01 35693873 Jones AV 2022-03-18 Ophthalmol Sci www.ncbi.nlm.nih.gov/pubmed/35693873 Evaluating a Causal Relationship between Complement Factor I Protein Level and Advanced Age-Related Macular Degeneration Using Mendelian Randomization. Circulating complement factor I levels 27,301 European ancestry individuals NA NR [NR] (imputed) 1 complement factor I measurement http://www.ebi.ac.uk/efo/EFO_0008099 GCST90105032 Genome-wide genotyping array 2022-09-20 35915169 Byun J 2022-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35915169 Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Lung cancer 26,683 European ancestry cases, 25,278 European ancestry controls, 7,062 East Asian ancestry cases, 5,372 East Asian ancestry controls, 1,987 African American cases, 3,774 African American controls 11,680 European ancestry cases, 898,929 European ancestry controls, 13,316 East Asian ancestry cases, 13,324 East Asian ancestry controls, 319 African American cases, 560 African American controls Affymetrix [NR] (imputed) 16 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90134661 Genome-wide genotyping array 2022-09-20 35915169 Byun J 2022-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35915169 Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Lung adenocarcinoma 9,791 European ancestry cases, 23,173 European ancestry controls, 4,630 East Asian ancestry cases, 5,372 East Asian ancestry controls, 844 African American cases, 3,774 African American controls 3,095 European ancestry cases, 436,443 European ancestry controls, 8,755 East Asian ancestry cases, 13,324 East Asian ancestry controls, 186 African American cases, 560 African American controls Affymetrix [NR] (imputed) 17 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST90134662 Genome-wide genotyping array 2022-09-20 35915169 Byun J 2022-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35915169 Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Squamous cell lung carcinoma 6,107 European ancestry cases, 23,173 European ancestry controls, 1,292 East Asian ancestry cases, 5,372 East Asian ancestry controls, 451 African American cases, 3,774 African American controls 1,607 European ancestry cases, 365,037 European ancestry controls, 3,857 East Asian ancestry cases, 13,324 East Asian ancestry controls, 75 African American cases, 560 African American controls Affymetrix [NR] (imputed) 9 squamous cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000708 GCST90134663 Genome-wide genotyping array 2022-09-20 35915169 Byun J 2022-08-01 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35915169 Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. Small cell lung carcinoma 2,267 European ancestry cases, 23,173 European ancestry controls, 99 East Asian ancestry cases, 5,372 East Asian ancestry controls, 116 African American cases, 3,774 African American controls 1,268 European ancestry cases, 365,282 European ancestry controls, 29 African American cases, 560 African American controls Affymetrix [NR] (imputed) 3 small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0000702 GCST90134664 Genome-wide genotyping array 2022-08-04 35479509 Thanaj M 2022-04-13 Nat Cardiovasc Res www.ncbi.nlm.nih.gov/pubmed/35479509 Genetic and environmental determinants of diastolic heart function. Maximum indexed left atrial volume 23,321 European ancestry individuals 10,924 European ancestry individuals Affymetrix [16705336] (imputed) 2 left atrial volume measurement http://www.ebi.ac.uk/efo/EFO_0600035 GCST90019012 Genome-wide genotyping array 2022-08-04 35479509 Thanaj M 2022-04-13 Nat Cardiovasc Res www.ncbi.nlm.nih.gov/pubmed/35479509 Genetic and environmental determinants of diastolic heart function. Longitudinal peak diastolic strain rate 23,321 European ancestry individuals 10,924 European ancestry individuals Affymetrix [16705336] (imputed) 4 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST90019013 Genome-wide genotyping array 2022-08-04 35479509 Thanaj M 2022-04-13 Nat Cardiovasc Res www.ncbi.nlm.nih.gov/pubmed/35479509 Genetic and environmental determinants of diastolic heart function. Radial peak diastolic strain rate 23,321 European ancestry individuals 10,924 European ancestry individuals Affymetrix [16705336] (imputed) 5 left ventricular diastolic function measurement http://www.ebi.ac.uk/efo/EFO_0008204 GCST90019014 Genome-wide genotyping array 2022-06-30 35351958 Lee CC 2022-03-30 J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35351958 Genome-wide association study of primary dysmenorrhea in the Taiwan Biobank validates associations near the NGF and IL1 gene loci. Primary dysmenorrhea 1,186 Taiwanese Han Chinese ancestry cases, 24,020 Taiwanese Han Chinese ancestry controls NA Affymetrix [4230987] (imputed) 4 Dysmenorrhea http://purl.obolibrary.org/obo/HP_0100607 GCST90105035 Genome-wide genotyping array 2022-07-29 35446786 Li Y 2022-04-21 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35446786 Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases. Serum uromodulin levels (antibody-based assay) 11,369 European ancestry individuals, 400 African American individuals, 2,216 Hispanic individuals NA Affymetrix, Illumina [10735251] (imputed) 8 uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0021778 GCST90129631 Genome-wide genotyping array 2022-07-29 35446786 Li Y 2022-04-21 JCI Insight www.ncbi.nlm.nih.gov/pubmed/35446786 Genome-wide studies reveal factors associated with circulating uromodulin and its relations with complex diseases. Serum uromodulin levels (aptamer-based assay) 18,070 European ancestry individuals NA Affymetrix, Illumina [8815558] (imputed) 16 uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0021778 GCST90129632 Genome-wide genotyping array 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Adhesion G protein-coupled receptor E2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 adhesion G protein-coupled receptor E2 measurement http://www.ebi.ac.uk/efo/EFO_0021892 GCST90137938 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Neutrophil collagenase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 matrix metalloproteinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0008466 GCST90137939 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Sonic hedgehog protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 sonic hedgehog protein measurement http://www.ebi.ac.uk/efo/EFO_0020746 GCST90137940 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Protein S100-A4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 protein S100-A4 measurement http://www.ebi.ac.uk/efo/EFO_0021893 GCST90137941 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Stem Cell Growth Factor-alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 stem cell growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020754 GCST90137942 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kallikrein-13 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kallikrein-13 measurement http://www.ebi.ac.uk/efo/EFO_0020512 GCST90137943 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leukocyte immunoglobulin-like receptor subfamily B member 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90137944 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement component C1q receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90137945 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Lipopolysaccharide-binding protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 lipopolysaccharide-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0021894 GCST90137946 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Formimidoyltransferase-cyclodeaminase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 formimidoyltransferase-cyclodeaminase measurement http://www.ebi.ac.uk/efo/EFO_0021895 GCST90137947 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Arylsulfatase A levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90137948 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-reactive protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90137527 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. IgA levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST90137505 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Inosine-5'-monophosphate dehydrogenase 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 inosine-5'-monophosphate dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008158 GCST90137506 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Alpha-2-macroglobulin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 alpha-2-macroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020138 GCST90137507 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Sialic acid-binding Ig-like lectin 14 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90137508 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Protein Wnt-7a levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 protein wnt-7a measurement http://www.ebi.ac.uk/efo/EFO_0020689 GCST90137509 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Aromatic-L-amino-acid decarboxylase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 aromatic-l-amino-acid decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0020161 GCST90137510 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Endoglin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 endoglin measurement http://www.ebi.ac.uk/efo/EFO_0008118 GCST90137511 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor ligand superfamily member 18 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 tumor necrosis factor ligand superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020795 GCST90137512 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Toll-like receptor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 toll-like receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020777 GCST90137513 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Lymphatic vessel endothelial hyaluronic acid receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 lymphatic vessel endothelial hyaluronic acid receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020539 GCST90137514 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Macrophage colony-stimulating factor 1 receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 macrophage colony-stimulating factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020547 GCST90137515 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement factor D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90137516 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. 14-3-3 protein beta/alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 14-3-3 protein family measurement http://www.ebi.ac.uk/efo/EFO_0020109 GCST90137517 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Plasminogen levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 plasma plasminogen measurement http://www.ebi.ac.uk/efo/EFO_0006309 GCST90137569 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Plasma kallikrein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 plasma kallikrein measurement http://www.ebi.ac.uk/efo/EFO_0008260 GCST90137570 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. P-selectin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90137571 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008053 GCST90137572 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Serum amyloid A-1 protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 serum amyloid A protein measurement http://www.ebi.ac.uk/efo/EFO_0004728 GCST90137573 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Urokinase-type plasminogen activator levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90137574 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Vitronectin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90137575 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Coagulation Factor V levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 coagulation factor V measurement http://www.ebi.ac.uk/efo/EFO_0008087 GCST90137576 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor ligand superfamily member 6, soluble form levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor ligand superfamily member 6, soluble form measurement http://www.ebi.ac.uk/efo/EFO_0020797 GCST90137577 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Nidogen-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 nidogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008249 GCST90137578 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Granulysin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90137579 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Hemoglobin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90137580 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Platelet-derived growth factor receptor alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 platelet-derived growth factor receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0021844 GCST90137581 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Granulocyte colony-stimulating factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90137582 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Gamma-enolase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 gamma-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021845 GCST90137583 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Human Chorionic Gonadotropin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90137584 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cystatin-C levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90137585 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Osteocalcin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90137586 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Superoxide dismutase [Mn], mitochondrial levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 superoxide dismutase [Mn], mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008294 GCST90137587 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Mucin-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90137518 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Angiogenin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90137519 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Fibroblast growth factor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 fibroblast growth factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008129 GCST90137520 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Estrogen receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 estrogen receptor measurement http://www.ebi.ac.uk/efo/EFO_0008125 GCST90137521 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. von Willebrand factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90137522 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90137523 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Insulin-like growth factor-binding protein 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 IGFBP-3 measurement http://www.ebi.ac.uk/efo/EFO_0004626 GCST90137524 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Insulin-like growth factor I levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 IGF-1 measurement http://www.ebi.ac.uk/efo/EFO_0004627 GCST90137525 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Vitamin K-dependent protein C levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90137526 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kallikrein-7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kallikrein-7 measurement http://www.ebi.ac.uk/efo/EFO_0008195 GCST90137528 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Epidermal growth factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90137529 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Hepatocyte growth factor receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 hepatocyte growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0008153 GCST90137530 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-1 receptor type 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90137531 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Alpha-1-antitrypsin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008327 GCST90137532 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Alpha-2-antiplasmin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 alpha-2-antiplasmin measurement http://www.ebi.ac.uk/efo/EFO_0020137 GCST90137533 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Alpha-2-HS-glycoprotein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90137534 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Angiotensinogen levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 angiotensinogen measurement http://www.ebi.ac.uk/efo/EFO_0008025 GCST90137535 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein E levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 apolipoprotein E measurement http://www.ebi.ac.uk/efo/EFO_0008029 GCST90137536 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein E (isoform E2) levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 apolipoprotein E isoform E2 measurement http://www.ebi.ac.uk/efo/EFO_0008028 GCST90137537 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Aspartate aminotransferase, cytoplasmic levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 aspartate aminotransferase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0008031 GCST90137538 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Beta-endorphin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90137539 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Plasma protease C1 inhibitor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90137540 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement C1q subcomponent levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90137541 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement C4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST90137542 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement C4b levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C4b measurement http://www.ebi.ac.uk/efo/EFO_0008092 GCST90137543 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement component C7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90137544 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement component C9 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90137545 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Calpastatin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 calpastatin measurement http://www.ebi.ac.uk/efo/EFO_0008065 GCST90137546 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Catalase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 catalase measurement http://www.ebi.ac.uk/efo/EFO_0008071 GCST90137547 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cathepsin B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90137548 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cathepsin D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cathepsin D measurement http://www.ebi.ac.uk/efo/EFO_0010611 GCST90137549 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cathepsin H levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90137550 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Endostatin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 endostatin measurement http://www.ebi.ac.uk/efo/EFO_0020347 GCST90137551 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Eotaxin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90137552 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement factor B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement factor B measurement http://www.ebi.ac.uk/efo/EFO_0008096 GCST90137553 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement factor H levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90137554 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Haptoglobin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90137555 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Heat shock protein beta-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 heat shock protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0010595 GCST90137556 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-16 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 16 measurement http://www.ebi.ac.uk/efo/EFO_0008173 GCST90137557 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 2 measurement http://www.ebi.ac.uk/efo/EFO_0008331 GCST90137558 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Laminin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 laminin measurement http://www.ebi.ac.uk/efo/EFO_0020528 GCST90137559 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Luteinizing hormone levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90137560 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Lysozyme C levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90137561 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 8 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 8 measurement http://www.ebi.ac.uk/efo/EFO_0008055 GCST90137562 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST90137563 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 3 measurement http://www.ebi.ac.uk/efo/EFO_0008051 GCST90137564 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interstitial collagenase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interstitial collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008193 GCST90137565 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Macrophage metalloelastase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 macrophage metalloelastase measurement http://www.ebi.ac.uk/efo/EFO_0008220 GCST90137566 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Matrilysin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 matrilysin measurement http://www.ebi.ac.uk/efo/EFO_0008227 GCST90137567 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Glucose-6-phosphate isomerase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 glucose-6-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020407 GCST90137568 Genome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Phosphatidylcholine diacyl C36:0 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 phosphatidylcholine 36:0 measurement http://www.ebi.ac.uk/efo/EFO_0021473 GCST90134389 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Hydroxyhexadecanoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 hydroxyhexadecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021807 GCST90134390 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Histidine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 5 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90134391 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Phosphatidylcholine acyl-alkyl C38:3 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 phosphatidylcholine 38:3 measurement http://www.ebi.ac.uk/efo/EFO_0010385 GCST90134392 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. lysoPhosphatidylcholine acyl C26:1 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 lysophosphatidylcholine 26:1 measurement http://www.ebi.ac.uk/efo/EFO_0021811 GCST90134393 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Asparagine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90134394 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Glutamine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90134395 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Phenylalanine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 3 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90134396 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Dodecenoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 3 dodecenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021808 GCST90134397 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Tetradecenoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 3 tetradecenoylcarnitine meaasurement http://www.ebi.ac.uk/efo/EFO_0021809 GCST90134398 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Sphingomyeline C16:0 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 sphingomyelin 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010391 GCST90134399 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Sphingomyeline C18:0 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 sphingomyelin 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010393 GCST90134400 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Sphingomyeline C24:0 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 sphingomyelin 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0010397 GCST90134401 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Sphingomyeline C24:1 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 sphingomyelin 24:1 measurement http://www.ebi.ac.uk/efo/EFO_0010398 GCST90134402 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Proline levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90134403 Genome-wide genotyping array, Exome-wide sequencing 2022-09-13 35893037 Pipal KV 2022-07-22 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/35893037 Susceptibility Loci for Type 2 Diabetes in the Ethnically Endogamous Indian Sindhi Population: A Pooled Blood Genome-Wide Association Study. Type 2 diabetes 418 Sindhi ancestry cases from endogamous families, 984 Sindhi ancestry controls from endogamous families NA Illumina [608550] 134 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90134620 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11409) 2,466 Black/admixed ancestry individuals NA Illumina [149269] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176515 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11410) 2,466 Black/admixed ancestry individuals NA Illumina [152131] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176516 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11412) 2,466 Black/admixed ancestry individuals NA Illumina [154257] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176517 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11412) 2,466 Black/admixed ancestry individuals NA Illumina [160576] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178966 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11418) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155463] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176518 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11440) 2,466 Black/admixed ancestry individuals NA Illumina [158507] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176519 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11450) 2,466 Black/admixed ancestry individuals NA Illumina [157706] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176520 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11461) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153346] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176521 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11469) 2,466 Black/admixed ancestry individuals NA Illumina [153504] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176522 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11471) 2,466 Black/admixed ancestry individuals NA Illumina [154633] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176523 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11471) 2,466 Black/admixed ancestry individuals NA Illumina [147427] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178737 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11485) 2,466 Black/admixed ancestry individuals NA Illumina [149784] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176524 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11506) 2,466 Black/admixed ancestry individuals NA Illumina [173466] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176525 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11516) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157198] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176526 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11519) 2,466 Black/admixed ancestry individuals NA Illumina [151465] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176527 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11522) 2,466 Black/admixed ancestry individuals NA Illumina [149534] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176528 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11533) 2,466 Black/admixed ancestry individuals NA Illumina [151439] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176529 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11535) 2,466 Black/admixed ancestry individuals NA Illumina [151564] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176530 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11537) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152583] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176531 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11545) 2,466 Black/admixed ancestry individuals NA Illumina [152585] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176532 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11547) 2,466 Black/admixed ancestry individuals NA Illumina [153685] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176533 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11551) 2,466 Black/admixed ancestry individuals NA Illumina [150657] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176534 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11554) 2,466 Black/admixed ancestry individuals NA Illumina [155885] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176535 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11554) 2,466 Black/admixed ancestry individuals NA Illumina [150455] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178738 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1156) 2,466 Black/admixed ancestry individuals NA Illumina [182289] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176536 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1157) 2,466 Black/admixed ancestry individuals NA Illumina [163285] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176537 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11571) 2,466 Black/admixed ancestry individuals NA Illumina [168734] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176538 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11581) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152194] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176539 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1159) 2,466 Black/admixed ancestry individuals NA Illumina [153418] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176540 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11590) 2,466 Black/admixed ancestry individuals NA Illumina [150034] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176541 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11595) 2,466 Black/admixed ancestry individuals NA Illumina [150989] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176542 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11595) 2,466 Black/admixed ancestry individuals NA Illumina [153876] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178739 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11597) 2,466 Black/admixed ancestry individuals NA Illumina [151946] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176543 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11611) 2,466 Black/admixed ancestry individuals NA Illumina [161123] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176544 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11620) 2,466 Black/admixed ancestry individuals NA Illumina [161102] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176545 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11626) 2,466 Black/admixed ancestry individuals NA Illumina [145720] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176546 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11626) 2,466 Black/admixed ancestry individuals NA Illumina [146839] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178740 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11627) 2,466 Black/admixed ancestry individuals NA Illumina [143508] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176547 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11627) 2,466 Black/admixed ancestry individuals NA Illumina [138100] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178967 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11630) 2,466 Black/admixed ancestry individuals NA Illumina [151271] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176548 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11633) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152197] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176549 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11635) 2,466 Black/admixed ancestry individuals NA Illumina [158032] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176550 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11649) 2,466 Black/admixed ancestry individuals NA Illumina [151972] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176551 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11649) 2,466 Black/admixed ancestry individuals NA Illumina [149834] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178741 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11679) 2,466 Black/admixed ancestry individuals NA Illumina [152155] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176552 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11682) 2,466 Black/admixed ancestry individuals NA Illumina [160774] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176553 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11682) 2,466 Black/admixed ancestry individuals NA Illumina [162753] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178968 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11716) 2,466 Black/admixed ancestry individuals NA Illumina [159700] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176554 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11739) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152144] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176555 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11745) 2,466 Black/admixed ancestry individuals NA Illumina [154968] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176556 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11240) 2,466 Black/admixed ancestry individuals NA Illumina [147464] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178963 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11242) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149000] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176497 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11279) 2,466 Black/admixed ancestry individuals NA Illumina [150121] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176498 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11279) 2,466 Black/admixed ancestry individuals NA Illumina [154473] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178733 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11285) 2,466 Black/admixed ancestry individuals NA Illumina [171270] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176499 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11289) 2,466 Black/admixed ancestry individuals NA Illumina [155550] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176500 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11297) 2,466 Black/admixed ancestry individuals NA Illumina [163523] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176501 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11298) 2,466 Black/admixed ancestry individuals NA Illumina [153559] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176502 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11307) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155868] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176503 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11312) 2,466 Black/admixed ancestry individuals NA Illumina [155528] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176504 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11315) 2,466 Black/admixed ancestry individuals NA Illumina [166599] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176505 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11315) 2,466 Black/admixed ancestry individuals NA Illumina [166194] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178734 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11332) 2,466 Black/admixed ancestry individuals NA Illumina [147406] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176506 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11344) 2,466 Black/admixed ancestry individuals NA Illumina [153956] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176507 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11345) 2,466 Black/admixed ancestry individuals NA Illumina [151479] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176508 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11350) 2,466 Black/admixed ancestry individuals NA Illumina [149459] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176509 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11350) 2,466 Black/admixed ancestry individuals NA Illumina [146901] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178964 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11361) 2,466 Black/admixed ancestry individuals NA Illumina [155007] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176510 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11361) 2,466 Black/admixed ancestry individuals NA Illumina [155828] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178965 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11365) 2,466 Black/admixed ancestry individuals NA Illumina [153758] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176511 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11365) 2,466 Black/admixed ancestry individuals NA Illumina [146126] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178735 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11366) 2,466 Black/admixed ancestry individuals NA Illumina [161140] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176512 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11366) 2,466 Black/admixed ancestry individuals NA Illumina [167531] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178736 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11368) 2,466 Black/admixed ancestry individuals NA Illumina [164041] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176513 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11391) 2,466 Black/admixed ancestry individuals NA Illumina [149409] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176514 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10128) 2,466 Black/admixed ancestry individuals NA Illumina [150635] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176372 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10135) 2,466 Black/admixed ancestry individuals NA Illumina [157306] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176373 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10135) 2,466 Black/admixed ancestry individuals NA Illumina [148535] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178925 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10136) 2,466 Black/admixed ancestry individuals NA Illumina [153257] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176374 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10138) 2,466 Black/admixed ancestry individuals NA Illumina [153957] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176375 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10139) 2,466 Black/admixed ancestry individuals NA Illumina [153142] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176376 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10141) 2,466 Black/admixed ancestry individuals NA Illumina [154707] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176377 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10146) 2,466 Black/admixed ancestry individuals NA Illumina [155190] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176378 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10148) 2,466 Black/admixed ancestry individuals NA Illumina [162622] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176379 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1015) 2,466 Black/admixed ancestry individuals NA Illumina [152465] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176380 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10151) 2,466 Black/admixed ancestry individuals NA Illumina [151481] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176381 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10154) 2,466 Black/admixed ancestry individuals NA Illumina [152139] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176382 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10154) 2,466 Black/admixed ancestry individuals NA Illumina [147726] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178926 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10157) 2,466 Black/admixed ancestry individuals NA Illumina [149112] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176383 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10179) 2,466 Black/admixed ancestry individuals NA Illumina [161364] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176384 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10188) 2,466 Black/admixed ancestry individuals NA Illumina [135735] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176385 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10188) 2,466 Black/admixed ancestry individuals NA Illumina [135106] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178721 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10201) 2,466 Black/admixed ancestry individuals NA Illumina [140022] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176386 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10226) 2,466 Black/admixed ancestry individuals NA Illumina [134581] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176387 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1023) 2,466 Black/admixed ancestry individuals NA Illumina [153351] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176388 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1024) 2,466 Black/admixed ancestry individuals NA Illumina [153147] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176389 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10241) 2,466 Black/admixed ancestry individuals NA Illumina [158097] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176390 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10245) 2,466 Black/admixed ancestry individuals NA Illumina [167177] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176391 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10245) 2,466 Black/admixed ancestry individuals NA Illumina [147947] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178927 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1027) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155553] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176392 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11025) 2,466 Black/admixed ancestry individuals NA Illumina [146062] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178959 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11028) 2,466 Black/admixed ancestry individuals NA Illumina [153029] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176479 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11028) 2,466 Black/admixed ancestry individuals NA Illumina [156564] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178730 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11032) 2,466 Black/admixed ancestry individuals NA Illumina [154823] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176480 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11032) 2,466 Black/admixed ancestry individuals NA Illumina [165979] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178960 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11054) 2,466 Black/admixed ancestry individuals NA Illumina [151371] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176481 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11083) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158253] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176482 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11087) 2,466 Black/admixed ancestry individuals NA Illumina [143595] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176483 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11091) 2,466 Black/admixed ancestry individuals NA Illumina [162865] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176484 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11092) 2,466 Black/admixed ancestry individuals NA Illumina [152818] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176485 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11104) 2,466 Black/admixed ancestry individuals NA Illumina [153769] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176486 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11109) 2,466 Black/admixed ancestry individuals NA Illumina [164660] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176487 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11109) 2,466 Black/admixed ancestry individuals NA Illumina [157406] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178961 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11114) 2,466 Black/admixed ancestry individuals NA Illumina [154635] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176488 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11119) 2,466 Black/admixed ancestry individuals NA Illumina [160259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176489 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11119) 2,466 Black/admixed ancestry individuals NA Illumina [163070] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178731 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11120) 2,466 Black/admixed ancestry individuals NA Illumina [610360] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178962 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11136) 2,466 Black/admixed ancestry individuals NA Illumina [153239] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176490 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11136) 2,466 Black/admixed ancestry individuals NA Illumina [146504] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178732 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11149) 2,466 Black/admixed ancestry individuals NA Illumina [155554] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176491 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11162) 2,466 Black/admixed ancestry individuals NA Illumina [153627] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176492 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11163) 2,466 Black/admixed ancestry individuals NA Illumina [157728] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176493 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1119) 2,466 Black/admixed ancestry individuals NA Illumina [153177] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176494 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11226) 2,466 Black/admixed ancestry individuals NA Illumina [152430] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176495 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11240) 2,466 Black/admixed ancestry individuals NA Illumina [150435] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176496 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10060) 2,466 Black/admixed ancestry individuals NA Illumina [149797] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178718 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10062) 2,466 Black/admixed ancestry individuals NA Illumina [163636] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176350 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10064) 2,466 Black/admixed ancestry individuals NA Illumina [158738] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176351 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10064) 2,466 Black/admixed ancestry individuals NA Illumina [161651] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178719 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10065) 2,466 Black/admixed ancestry individuals NA Illumina [152180] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176352 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10068) 2,466 Black/admixed ancestry individuals NA Illumina [150285] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176353 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10070) 2,466 Black/admixed ancestry individuals NA Illumina [150759] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176354 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10071) 2,466 Black/admixed ancestry individuals NA Illumina [165780] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176355 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10076) 2,466 Black/admixed ancestry individuals NA Illumina [153204] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176356 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10082) 2,466 Black/admixed ancestry individuals NA Illumina [160405] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176357 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10083) 2,466 Black/admixed ancestry individuals NA Illumina [153882] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176358 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10087) 2,466 Black/admixed ancestry individuals NA Illumina [152758] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176359 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10088) 2,466 Black/admixed ancestry individuals NA Illumina [151378] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176360 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10096) 2,466 Black/admixed ancestry individuals NA Illumina [172010] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176361 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1010) 2,466 Black/admixed ancestry individuals NA Illumina [164608] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176362 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1010) 2,466 Black/admixed ancestry individuals NA Illumina [166346] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178720 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10100) 2,466 Black/admixed ancestry individuals NA Illumina [154247] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176363 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10102) 2,466 Black/admixed ancestry individuals NA Illumina [150876] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176364 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10104) 2,466 Black/admixed ancestry individuals NA Illumina [151512] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176365 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10105) 2,466 Black/admixed ancestry individuals NA Illumina [148646] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176366 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10116) 2,466 Black/admixed ancestry individuals NA Illumina [151611] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176367 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10118) 2,466 Black/admixed ancestry individuals NA Illumina [155125] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176368 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10119) 2,466 Black/admixed ancestry individuals NA Illumina [152311] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176369 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1012) 2,466 Black/admixed ancestry individuals NA Illumina [154309] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176370 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10127) 2,466 Black/admixed ancestry individuals NA Illumina [168071] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176371 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10948) 2,466 Black/admixed ancestry individuals NA Illumina [148621] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176461 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10948) 2,466 Black/admixed ancestry individuals NA Illumina [144518] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178954 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10949) 2,466 Black/admixed ancestry individuals NA Illumina [171526] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176462 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10949) 2,466 Black/admixed ancestry individuals NA Illumina [161951] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178728 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1095) 2,466 Black/admixed ancestry individuals NA Illumina [152016] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176463 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10958) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [164901] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176464 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1096) 2,466 Black/admixed ancestry individuals NA Illumina [152602] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176465 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10960) 2,466 Black/admixed ancestry individuals NA Illumina [175835] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178955 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10963) 2,466 Black/admixed ancestry individuals NA Illumina [150997] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176466 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10969) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150979] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176467 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1097) 2,466 Black/admixed ancestry individuals NA Illumina [152382] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176468 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1097) 2,466 Black/admixed ancestry individuals NA Illumina [141468] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178956 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10973) 2,466 Black/admixed ancestry individuals NA Illumina [158942] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176469 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10980) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159460] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176470 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10981) 2,466 Black/admixed ancestry individuals NA Illumina [156906] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176471 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10987) 2,466 Black/admixed ancestry individuals NA Illumina [149618] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176472 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10990) 2,466 Black/admixed ancestry individuals NA Illumina [152175] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176473 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10990) 2,466 Black/admixed ancestry individuals NA Illumina [152365] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178729 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10992) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155473] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176474 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI10993) 2,466 Black/admixed ancestry individuals NA Illumina [169719] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176475 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1100) 2,466 Black/admixed ancestry individuals NA Illumina [151776] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176476 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1102) 2,466 Black/admixed ancestry individuals NA Illumina [171548] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176477 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1102) 2,466 Black/admixed ancestry individuals NA Illumina [168514] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178957 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11024) 2,466 Black/admixed ancestry individuals NA Illumina [180653] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178958 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI11025) 2,466 Black/admixed ancestry individuals NA Illumina [163463] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176478 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N1-acetylspermidine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148211] 1 N1-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0801193 GCST90176300 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N1-methyl-2-pyridone-5-carboxamide levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158196] 1 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90176301 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N2,n2-dimethylguanosine levels 2,466 Black/admixed ancestry individuals NA Illumina [155119] 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90176302 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N4-acetylcytidine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [165698] 2 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90176303 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N6-acetyllysine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160888] 2 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90176304 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N6-methyllysine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [219480] 4 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90176305 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N6,N6-dimethyllysine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [190285] 6 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90176306 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N6,n6,n6-trimethyllysine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158970] 1 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90176307 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Na C34:1 DAG or TAG fragment levels 2,466 Black/admixed ancestry individuals NA Illumina [152273] 0 Na_C34:1 DAG_or_TAG_fragment measurement http://www.ebi.ac.uk/efo/EFO_0801194 GCST90176308 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Na C34:2 DAG or TAG fragment levels 2,466 Black/admixed ancestry individuals NA Illumina [153577] 0 Na_C34:2 DAG_or_TAG_fragment measurement http://www.ebi.ac.uk/efo/EFO_0801195 GCST90176309 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C34:2 DAG or TAG fragment levels 2,466 Black/admixed ancestry individuals NA Illumina [150876] 0 NH4_C34:2 DAG_or_TAG_fragment measurement http://www.ebi.ac.uk/efo/EFO_0801196 GCST90176310 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C34:3 DAG or TAG fragment levels 2,466 Black/admixed ancestry individuals NA Illumina [155516] 0 NH4_C34:3 DAG_or_TAG_fragment measurement http://www.ebi.ac.uk/efo/EFO_0801197 GCST90176311 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C36:2 DAG or TAG fragment levels 2,466 Black/admixed ancestry individuals NA Illumina [153140] 0 NH4_C36:2 DAG_or_TAG_fragment measurement http://www.ebi.ac.uk/efo/EFO_0801198 GCST90176312 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C36:3 DAG or TAG fragment levels 2,466 Black/admixed ancestry individuals NA Illumina [153333] 0 NH4_C36:3 DAG_or_TAG_fragment measurement http://www.ebi.ac.uk/efo/EFO_0801199 GCST90176313 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. DG(36:4) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154476] 1 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90176314 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. DG(38:5) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159660] 1 diacylglycerol 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0020067 GCST90176315 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C44:1 TAG levels 2,466 Black/admixed ancestry individuals NA Illumina [176150] 0 NH4_C44:1 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801202 GCST90176316 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C44:2 TAG levels 2,466 Black/admixed ancestry individuals NA Illumina [152296] 0 NH4_C44:2 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801203 GCST90176317 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C46:2 TAG levels 2,466 Black/admixed ancestry individuals NA Illumina [149539] 0 NH4_C46:2 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801204 GCST90176318 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NH4 C46:3 TAG levels 2,466 Black/admixed ancestry individuals NA Illumina [148544] 0 NH4_C46:3 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801205 GCST90176319 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Niacinamide levels 2,466 Black/admixed ancestry individuals NA Illumina [153229] 0 niacinamide measurement http://www.ebi.ac.uk/efo/EFO_0010511 GCST90176320 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. NMMA levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154043] 1 NMMA measurement http://www.ebi.ac.uk/efo/EFO_0801206 GCST90176321 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oleoyl glycine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151935] 1 oleoyl glycine measurement http://www.ebi.ac.uk/efo/EFO_0801207 GCST90176095 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oleoyl glycine levels 2,466 Black/admixed ancestry individuals NA Illumina [150113] 0 oleoyl glycine measurement http://www.ebi.ac.uk/efo/EFO_0801207 GCST90176322 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oleoyl leucine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154457] 1 oleoyl leucine measurement http://www.ebi.ac.uk/efo/EFO_0801208 GCST90176096 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine plasmalogen 36:5 levels 2,466 Black/admixed ancestry individuals NA Illumina [154263] 0 C36:5 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801141 GCST90176226 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine plasmalogen C36:5 levels 2,466 Black/admixed ancestry individuals NA Illumina [149766] 0 C36:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801142 GCST90176227 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine C38:4 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158789] 1 C38:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801143 GCST90176228 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine plasmalogen C38:5 levels 2,466 Black/admixed ancestry individuals NA Illumina [149850] 0 C38:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801144 GCST90176229 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine plasmalogen C38:6 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163703] 1 C38:6 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801145 GCST90176230 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine (38:6) levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157153] 1 C38:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801146 GCST90176231 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine plasmalogen C38:6 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152758] 1 C38:6 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801147 GCST90176232 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylcholine plasmalogen C38:7 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154654] 1 C38:7 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801148 GCST90176233 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine plasmalogen C38:7 levels 2,466 Black/admixed ancestry individuals NA Illumina [156746] 0 C38:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801149 GCST90176234 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C4 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154563] 1 butyrylcarnitine (C4) measurement http://www.ebi.ac.uk/efo/EFO_0800201 GCST90176236 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C4-OH levels 2,466 Black/admixed ancestry individuals NA Illumina [154676] 0 C4-OH carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801150 GCST90176235 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine (40:6) levels 2,466 Black/admixed ancestry individuals NA Illumina [152706] 0 C40:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801151 GCST90176237 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphatidylethanolamine plasmalogen C40:7 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152050] 1 C40:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801152 GCST90176238 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C5 levels 2,466 Black/admixed ancestry individuals NA Illumina [151612] 0 C5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801153 GCST90176239 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C5:1 levels 2,466 Black/admixed ancestry individuals NA Illumina [152735] 0 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90176240 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C6 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158678] 1 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90176241 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C7 levels 2,466 Black/admixed ancestry individuals NA Illumina [160591] 0 C7 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801154 GCST90176242 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C8 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163648] 2 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90176243 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine C9 levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150775] 2 C9 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801155 GCST90176244 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Caffeine levels 2,466 Black/admixed ancestry individuals NA Illumina [148863] 0 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90176245 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Carnitine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155828] 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90176246 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Choline levels 2,466 Black/admixed ancestry individuals NA Illumina [153968] 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90176247 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Citric acid/Isocitric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [155940] 0 citric acid/isocitric acid measurement http://www.ebi.ac.uk/efo/EFO_0801156 GCST90176038 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Citrulline levels 2,466 Black/admixed ancestry individuals NA Illumina [153914] 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90176039 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Citrulline levels 2,466 Black/admixed ancestry individuals NA Illumina [152024] 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90176248 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metronidazole levels 2,466 Black/admixed ancestry individuals NA Illumina [150263] 0 metronidazole measurement http://www.ebi.ac.uk/efo/EFO_0801180 GCST90178924 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Myristoleate levels 2,466 Black/admixed ancestry individuals NA Illumina [149274] 0 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90176287 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetyl-L-alanine levels 2,466 Black/admixed ancestry individuals NA Illumina [162183] 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90176091 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetyl-L-aspartic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [145999] 0 N-acetyl-L-aspartic acid measurement http://www.ebi.ac.uk/efo/EFO_0801181 GCST90176092 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetyl-L-glutamic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161002] 1 N-acetyl-L-glutamic acid measurement http://www.ebi.ac.uk/efo/EFO_0801182 GCST90176093 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetyl-L-glutamine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159456] 2 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90176094 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetylalanine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156860] 1 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90176288 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetylaspartic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158324] 1 N-acetylaspartic acid measurement http://www.ebi.ac.uk/efo/EFO_0801183 GCST90176289 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetylhistidine levels 2,466 Black/admixed ancestry individuals NA Illumina [152524] 0 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90176290 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetylleucine levels 2,466 Black/admixed ancestry individuals NA Illumina [159066] 0 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90176291 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetylornithine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [170149] 1 GCST90176292 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetylputrescine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158540] 1 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90176293 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetylserine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156722] 1 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90176294 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-acetyltryptophan levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156797] 1 N-acetyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800018 GCST90176295 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-alpha-acetylarginine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [165195] 1 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90176296 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-arachidonoyl dopamine levels 2,466 Black/admixed ancestry individuals NA Illumina [160453] 0 N-arachidonoyl dopamine measurement http://www.ebi.ac.uk/efo/EFO_0801184 GCST90176116 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-arachidonoyl taurine levels 2,466 Black/admixed ancestry individuals NA Illumina [163692] 0 N-arachidonoyl taurine measurement http://www.ebi.ac.uk/efo/EFO_0801185 GCST90176117 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-carbamoyl-beta-alanine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150423] 1 N-carbamoyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0801186 GCST90176297 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-docosanoyl taurine levels 2,466 Black/admixed ancestry individuals NA Illumina [155261] 0 N-docosanoyl taurine measurement http://www.ebi.ac.uk/efo/EFO_0801187 GCST90176118 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-lauroylglycine levels 2,466 Black/admixed ancestry individuals NA Illumina [157180] 0 N-lauroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0801188 GCST90176298 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-lignoceroyl taurine levels 2,466 Black/admixed ancestry individuals NA Illumina [153616] 0 N-lignoceroyl taurine measurement http://www.ebi.ac.uk/efo/EFO_0801189 GCST90176119 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-methylproline levels 2,466 Black/admixed ancestry individuals NA Illumina [150306] 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90176299 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-nervonoyl taurine levels 2,466 Black/admixed ancestry individuals NA Illumina [160085] 0 N-nervonoyl taurine measurement http://www.ebi.ac.uk/efo/EFO_0801190 GCST90176120 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-oleoyltaurine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151085] 1 N-oleoyl taurine measurement http://www.ebi.ac.uk/efo/EFO_0801191 GCST90176121 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. N-palmitoyltaurine levels 2,466 Black/admixed ancestry individuals NA Illumina [152253] 0 N-palmitoyl taurine measurement http://www.ebi.ac.uk/efo/EFO_0801192 GCST90176122 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Cortisol levels 2,466 Black/admixed ancestry individuals NA Illumina [170874] 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90176249 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Cortisone levels 2,466 Black/admixed ancestry individuals NA Illumina [162352] 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90176250 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Cotinine levels 2,466 Black/admixed ancestry individuals NA Illumina [148005] 0 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST90176251 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Creatine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163571] 1 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90176252 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Creatinine levels 2,466 Black/admixed ancestry individuals NA Illumina [157046] 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90176253 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Cyclic-AMP levels 2,466 Black/admixed ancestry individuals NA Illumina [149886] 0 Cyclic AMP measurement http://www.ebi.ac.uk/efo/EFO_0021580 GCST90176040 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Cystine levels 2,466 Black/admixed ancestry individuals NA Illumina [157169] 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90176254 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. D-Gluconic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [151425] 0 Gluconic acid measurement http://www.ebi.ac.uk/efo/EFO_0021598 GCST90176042 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Deoxycholic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [153547] 0 Deoxycholic acid measurement http://www.ebi.ac.uk/efo/EFO_0021593 GCST90176041 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. DHA levels 2,466 Black/admixed ancestry individuals NA Illumina [153458] 0 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90176100 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Diacetylspermine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152731] 1 diacetylspermine measurement http://www.ebi.ac.uk/efo/EFO_0801157 GCST90176255 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Dimethylglycine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158883] 1 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90176256 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. DMGV levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163948] 1 DMGV measurement http://www.ebi.ac.uk/efo/EFO_0801158 GCST90176257 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Ectoine levels 2,466 Black/admixed ancestry individuals NA Illumina [148910] 0 ectoine measurement http://www.ebi.ac.uk/efo/EFO_0800953 GCST90176258 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. EPA levels 2,466 Black/admixed ancestry individuals NA Illumina [155656] 0 eicosapentaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007760 GCST90176101 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Fumaric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [161894] 0 fumaric acid measurement http://www.ebi.ac.uk/efo/EFO_0801159 GCST90176043 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. GABA levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155196] 1 GABA measurement http://www.ebi.ac.uk/efo/EFO_0801160 GCST90176259 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Gabapentin levels 2,466 Black/admixed ancestry individuals NA Illumina [142169] 0 gabapentin measurement http://www.ebi.ac.uk/efo/EFO_0801161 GCST90176260 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Gabapentin levels 2,466 Black/admixed ancestry individuals NA Illumina [146889] 0 gabapentin measurement http://www.ebi.ac.uk/efo/EFO_0801161 GCST90178920 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glucose/Fructose/Galactose waterloss levels 2,466 Black/admixed ancestry individuals NA Illumina [161398] 0 carbohydrate measurement http://www.ebi.ac.uk/efo/EFO_0004998 GCST90176044 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glutamate levels 2,466 Black/admixed ancestry individuals NA Illumina [151786] 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90176261 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glutamic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [157451] 0 L-Glutamic acid measurement http://www.ebi.ac.uk/efo/EFO_0021616 GCST90176089 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glutamine levels 2,466 Black/admixed ancestry individuals NA Illumina [149229] 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90176262 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Reduced glutathione levels 2,466 Black/admixed ancestry individuals NA Illumina [150661] 0 reduced glutathione measurement http://www.ebi.ac.uk/efo/EFO_0801162 GCST90176045 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glyceric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [155763] 0 glyceric acid measurement http://www.ebi.ac.uk/efo/EFO_0801163 GCST90176046 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6196) 2,466 Black/admixed ancestry individuals NA Illumina [147805] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178030 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6199) 2,466 Black/admixed ancestry individuals NA Illumina [151544] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178031 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI620) 2,466 Black/admixed ancestry individuals NA Illumina [154263] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178032 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6200) 2,466 Black/admixed ancestry individuals NA Illumina [150152] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178033 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6201) 2,466 Black/admixed ancestry individuals NA Illumina [151294] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178034 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6203) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162007] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178035 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6204) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157805] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178036 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6205) 2,466 Black/admixed ancestry individuals NA Illumina [150668] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178037 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI621) 2,466 Black/admixed ancestry individuals NA Illumina [153670] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178038 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI624) 2,466 Black/admixed ancestry individuals NA Illumina [151916] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178039 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6289) 2,466 Black/admixed ancestry individuals NA Illumina [169122] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178054 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6298) 2,466 Black/admixed ancestry individuals NA Illumina [151927] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178055 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6300) 2,466 Black/admixed ancestry individuals NA Illumina [174191] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178056 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6301) 2,466 Black/admixed ancestry individuals NA Illumina [154800] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178057 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6302) 2,466 Black/admixed ancestry individuals NA Illumina [152534] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178058 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6248) 2,466 Black/admixed ancestry individuals NA Illumina [153034] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178041 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI625) 2,466 Black/admixed ancestry individuals NA Illumina [163219] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178042 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6252) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151739] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178043 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6310) 2,466 Black/admixed ancestry individuals NA Illumina [158599] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178062 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6312) 2,466 Black/admixed ancestry individuals NA Illumina [151059] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178063 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI627) 2,466 Black/admixed ancestry individuals NA Illumina [153929] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178046 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6314) 2,466 Black/admixed ancestry individuals NA Illumina [167082] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178064 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6271) 2,466 Black/admixed ancestry individuals NA Illumina [149232] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178048 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6320) 2,466 Black/admixed ancestry individuals NA Illumina [150772] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178066 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6325) 2,466 Black/admixed ancestry individuals NA Illumina [150383] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178067 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6326) 2,466 Black/admixed ancestry individuals NA Illumina [159921] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178068 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6329) 2,466 Black/admixed ancestry individuals NA Illumina [151908] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178069 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI628) 2,466 Black/admixed ancestry individuals NA Illumina [154382] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178052 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6331) 2,466 Black/admixed ancestry individuals NA Illumina [156566] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178071 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6333) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154645] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178072 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6335) 2,466 Black/admixed ancestry individuals NA Illumina [154041] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178073 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI634) 2,466 Black/admixed ancestry individuals NA Illumina [145818] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178074 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6342) 2,466 Black/admixed ancestry individuals NA Illumina [157473] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178075 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6343) 2,466 Black/admixed ancestry individuals NA Illumina [169287] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178076 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6347) 2,466 Black/admixed ancestry individuals NA Illumina [150279] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178077 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glycerol 3-phosphate levels 2,466 Black/admixed ancestry individuals NA Illumina [165738] 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90176047 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glycine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158285] 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90176263 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glycochenodeoxycholic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153641] 1 Glycochenodeoxycholic acid measurement http://www.ebi.ac.uk/efo/EFO_0021599 GCST90176048 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glycocholate levels 2,466 Black/admixed ancestry individuals NA Illumina [150880] 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90176264 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glycocholic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [152377] 0 glycocholic acid measurement http://www.ebi.ac.uk/efo/EFO_0010492 GCST90176049 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glycodeoxycholate/glycochenodeoxycholate levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153704] 1 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90176265 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Glyoxylic Acid levels 2,466 Black/admixed ancestry individuals NA Illumina [159367] 0 glyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801164 GCST90176050 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Guanine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159198] 1 guanine measurement http://www.ebi.ac.uk/efo/EFO_0801165 GCST90176266 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. HETE levels 2,466 Black/admixed ancestry individuals NA Illumina [156755] 0 HETE measurement http://www.ebi.ac.uk/efo/EFO_0801166 GCST90176115 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hippurate levels 2,466 Black/admixed ancestry individuals NA Illumina [152267] 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90176267 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hippuric acid levels 2,466 Black/admixed ancestry individuals NA Illumina [150541] 0 hippuric acid measurement http://www.ebi.ac.uk/efo/EFO_0010496 GCST90176051 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Histidine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150294] 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90176268 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Homoarginine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156401] 2 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST90176269 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Homocysteine levels 2,466 Black/admixed ancestry individuals NA Illumina [174538] 0 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST90176270 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Homocysteine levels 2,466 Black/admixed ancestry individuals NA Illumina [159080] 0 homocysteine measurement http://www.ebi.ac.uk/efo/EFO_0004578 GCST90178716 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Homogentisic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [168239] 0 homogentisic acid measurement http://www.ebi.ac.uk/efo/EFO_0801167 GCST90176052 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hydroxycotinine levels 2,466 Black/admixed ancestry individuals NA Illumina [146990] 0 hydroxycotinine measurement http://www.ebi.ac.uk/efo/EFO_0800964 GCST90176271 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hydroxycotinine levels 2,466 Black/admixed ancestry individuals NA Illumina [147175] 0 hydroxycotinine measurement http://www.ebi.ac.uk/efo/EFO_0800964 GCST90178921 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hydroxyectoine levels 2,466 Black/admixed ancestry individuals NA Illumina [163130] 0 hydroxyectoine measurement http://www.ebi.ac.uk/efo/EFO_0801168 GCST90176272 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hydroxyphenylpyruvic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [160814] 0 hydroxyphenylpyruvic acid measurement http://www.ebi.ac.uk/efo/EFO_0801169 GCST90176090 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hydroxyproline levels 2,466 Black/admixed ancestry individuals NA Illumina [152486] 0 hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0010498 GCST90176273 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hypoxanthine levels 2,466 Black/admixed ancestry individuals NA Illumina [163045] 0 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90176053 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Hypoxanthine levels 2,466 Black/admixed ancestry individuals NA Illumina [168504] 0 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90176274 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Imidazole propionate levels 2,466 Black/admixed ancestry individuals NA Illumina [148996] 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90176275 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Indole-3-carboxylic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [165918] 0 indole-3-carboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801170 GCST90176054 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oleoyl phenylalanine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [166848] 1 oleoyl phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0801209 GCST90176097 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oleoyl serine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148928] 1 oleoyl serine measurement http://www.ebi.ac.uk/efo/EFO_0801210 GCST90176098 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Ornithine levels 2,466 Black/admixed ancestry individuals NA Illumina [152427] 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90176323 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Orotic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157634] 2 orotic acid measurement http://www.ebi.ac.uk/efo/EFO_0010516 GCST90176065 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oxalic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [150100] 0 oxalic acid measurement http://www.ebi.ac.uk/efo/EFO_0801211 GCST90176066 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oxaloacetic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157920] 2 oxaloacetic acid measurement http://www.ebi.ac.uk/efo/EFO_0801212 GCST90176067 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Oxypurinol levels 2,466 Black/admixed ancestry individuals NA Illumina [186443] 0 oxypurinol measurement http://www.ebi.ac.uk/efo/EFO_0801213 GCST90176125 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Palmitic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [169540] 0 Palmitic acid measurement http://www.ebi.ac.uk/efo/EFO_0021660 GCST90176103 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pantothenate levels 2,466 Black/admixed ancestry individuals NA Illumina [157300] 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90176324 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pantothenic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [155027] 0 pantothenic acid mesurement http://www.ebi.ac.uk/efo/EFO_0010519 GCST90176068 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phenylacetylglutamine levels 2,466 Black/admixed ancestry individuals NA Illumina [159802] 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90176325 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phenylalanine levels 2,466 Black/admixed ancestry individuals NA Illumina [155476] 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90176326 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phenylalanine-d8 levels 2,466 Black/admixed ancestry individuals NA Illumina [156590] 0 phenylalanine-d8 measurement http://www.ebi.ac.uk/efo/EFO_0801214 GCST90176327 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphocholine levels 2,466 Black/admixed ancestry individuals NA Illumina [153573] 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90176328 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Phosphocreatine levels 2,466 Black/admixed ancestry individuals NA Illumina [152601] 0 phosphocreatine measurement http://www.ebi.ac.uk/efo/EFO_0010521 GCST90176069 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Pipecolic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [171562] 0 L-Pipecolic acid measurement http://www.ebi.ac.uk/efo/EFO_0021626 GCST90176329 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6160) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152337] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178021 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6166) 2,466 Black/admixed ancestry individuals NA Illumina [150063] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178023 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI617) 2,466 Black/admixed ancestry individuals NA Illumina [153370] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178024 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI618) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160198] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178025 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6181) 2,466 Black/admixed ancestry individuals NA Illumina [158580] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178026 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6181) 2,466 Black/admixed ancestry individuals NA Illumina [140376] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179081 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI619) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152780] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178027 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6191) 2,466 Black/admixed ancestry individuals NA Illumina [145978] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178028 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6195) 2,466 Black/admixed ancestry individuals NA Illumina [151684] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178029 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Indole-3-lactic acid levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157173] 1 indole-3-lactic acid measurement http://www.ebi.ac.uk/efo/EFO_0801171 GCST90176055 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Indole-3-propanoic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [151109] 0 indole-3-propanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801172 GCST90176056 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Indoxyl-sulfate levels 2,466 Black/admixed ancestry individuals NA Illumina [149754] 0 indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010502 GCST90176057 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Inosine levels 2,466 Black/admixed ancestry individuals NA Illumina [152278] 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90176058 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Isoleucine levels 2,466 Black/admixed ancestry individuals NA Illumina [151564] 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90176276 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Keto-isocaproic acid/Keto-methylvalerate levels 2,466 Black/admixed ancestry individuals NA Illumina [166502] 0 keto-isocaproic acid KIC / keto-methylvalerate KMV measurement http://www.ebi.ac.uk/efo/EFO_0801173 GCST90176059 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Kynurenic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [154503] 0 kynurenic acid measurement http://www.ebi.ac.uk/efo/EFO_0010506 GCST90176060 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Kynurenic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [170487] 0 kynurenic acid measurement http://www.ebi.ac.uk/efo/EFO_0010506 GCST90176277 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Kynurenine levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153114] 1 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90176061 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lactic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [165403] 0 lactic acid measurement http://www.ebi.ac.uk/efo/EFO_0801174 GCST90176062 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Leucine levels 2,466 Black/admixed ancestry individuals NA Illumina [150234] 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90176278 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Linoleic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [157736] 0 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90176102 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Linoleoyl ethanolamide levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154319] 1 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90176279 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lisinopril levels 2,466 Black/admixed ancestry individuals NA Illumina [159447] 0 lisinopril measurement http://www.ebi.ac.uk/efo/EFO_0801175 GCST90176124 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Lysine levels 2,466 Black/admixed ancestry individuals NA Illumina [153406] 0 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90176280 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Malic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [158153] 0 L-Malic acid measurement http://www.ebi.ac.uk/efo/EFO_0021622 GCST90176063 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Malonic acid levels 2,466 Black/admixed ancestry individuals NA Illumina [155898] 0 malonic acid measurement http://www.ebi.ac.uk/efo/EFO_0801176 GCST90176064 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metformin levels 2,466 Black/admixed ancestry individuals NA Illumina [147327] 0 metformin measurement http://www.ebi.ac.uk/efo/EFO_0801177 GCST90176281 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metformin levels 2,466 Black/admixed ancestry individuals NA Illumina [155118] 0 metformin measurement http://www.ebi.ac.uk/efo/EFO_0801177 GCST90178922 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Methionine levels 2,466 Black/admixed ancestry individuals NA Illumina [159543] 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90176282 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Methionine sulfoxide levels 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153462] 1 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90176283 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Methylhistidine levels 2,466 Black/admixed ancestry individuals NA Illumina [164143] 0 methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0801178 GCST90176284 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metoprolol levels 2,466 Black/admixed ancestry individuals NA Illumina [141952] 0 metoprolol measurement http://www.ebi.ac.uk/efo/EFO_0801179 GCST90176285 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metoprolol levels 2,466 Black/admixed ancestry individuals NA Illumina [165798] 0 metoprolol measurement http://www.ebi.ac.uk/efo/EFO_0801179 GCST90178923 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metronidazole levels 2,466 Black/admixed ancestry individuals NA Illumina [169282] 0 metronidazole measurement http://www.ebi.ac.uk/efo/EFO_0801180 GCST90176286 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6243) 2,466 Black/admixed ancestry individuals NA Illumina [143616] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178040 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6243) 2,466 Black/admixed ancestry individuals NA Illumina [144024] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179082 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6305) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152890] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178059 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6307) 2,466 Black/admixed ancestry individuals NA Illumina [156529] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178060 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6308) 2,466 Black/admixed ancestry individuals NA Illumina [157249] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178061 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6256) 2,466 Black/admixed ancestry individuals NA Illumina [141918] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178044 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI626) 2,466 Black/admixed ancestry individuals NA Illumina [154270] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178045 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6312) 2,466 Black/admixed ancestry individuals NA Illumina [146057] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179083 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6270) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158022] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178047 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI632) 2,466 Black/admixed ancestry individuals NA Illumina [158648] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178065 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6273) 2,466 Black/admixed ancestry individuals NA Illumina [160098] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178049 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6276) 2,466 Black/admixed ancestry individuals NA Illumina [153933] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178050 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6277) 2,466 Black/admixed ancestry individuals NA Illumina [148546] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178051 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI633) 2,466 Black/admixed ancestry individuals NA Illumina [155496] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178070 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6287) 2,466 Black/admixed ancestry individuals NA Illumina [166273] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178053 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6671) 2,466 Black/admixed ancestry individuals NA Illumina [166225] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178179 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6672) 2,466 Black/admixed ancestry individuals NA Illumina [167841] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178180 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6673) 2,466 Black/admixed ancestry individuals NA Illumina [164163] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178181 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6674) 2,466 Black/admixed ancestry individuals NA Illumina [164200] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178182 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6675) 2,466 Black/admixed ancestry individuals NA Illumina [166501] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178183 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6676) 2,466 Black/admixed ancestry individuals NA Illumina [161104] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178184 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6677) 2,466 Black/admixed ancestry individuals NA Illumina [169289] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178185 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6678) 2,466 Black/admixed ancestry individuals NA Illumina [181015] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178186 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6679) 2,466 Black/admixed ancestry individuals NA Illumina [163571] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178187 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6680) 2,466 Black/admixed ancestry individuals NA Illumina [159768] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178188 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6685) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155006] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178189 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6688) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155567] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178190 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6691) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157137] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178191 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6693) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157113] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178192 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6696) 2,466 Black/admixed ancestry individuals NA Illumina [156692] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178193 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6698) 2,466 Black/admixed ancestry individuals NA Illumina [154379] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178194 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6701) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151338] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178195 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6703) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152723] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178196 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6704) 2,466 Black/admixed ancestry individuals NA Illumina [151459] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178197 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6707) 2,466 Black/admixed ancestry individuals NA Illumina [149685] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178198 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI671) 2,466 Black/admixed ancestry individuals NA Illumina [156056] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178199 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6715) 2,466 Black/admixed ancestry individuals NA Illumina [153997] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178200 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI672) 2,466 Black/admixed ancestry individuals NA Illumina [154283] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178201 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6721) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152415] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178202 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6725) 2,466 Black/admixed ancestry individuals NA Illumina [170027] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178203 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6726) 2,466 Black/admixed ancestry individuals NA Illumina [152139] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178204 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6728) 2,466 Black/admixed ancestry individuals NA Illumina [155123] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178205 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI673) 2,466 Black/admixed ancestry individuals NA Illumina [156353] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178206 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6741) 2,466 Black/admixed ancestry individuals NA Illumina [154051] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178207 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6743) 2,466 Black/admixed ancestry individuals NA Illumina [158586] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178208 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6748) 2,466 Black/admixed ancestry individuals NA Illumina [151784] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178209 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13676) 2,466 Black/admixed ancestry individuals NA Illumina [155941] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176746 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13685) 2,466 Black/admixed ancestry individuals NA Illumina [153795] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176747 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13692) 2,466 Black/admixed ancestry individuals NA Illumina [168202] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176748 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13701) 2,466 Black/admixed ancestry individuals NA Illumina [154685] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176749 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13703) 2,466 Black/admixed ancestry individuals NA Illumina [149191] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176750 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13715) 2,466 Black/admixed ancestry individuals NA Illumina [151960] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176751 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13720) 2,466 Black/admixed ancestry individuals NA Illumina [154425] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176752 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13735) 2,466 Black/admixed ancestry individuals NA Illumina [151686] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176753 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13736) 2,466 Black/admixed ancestry individuals NA Illumina [173496] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176754 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1374) 2,466 Black/admixed ancestry individuals NA Illumina [152554] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176755 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13740) 2,466 Black/admixed ancestry individuals NA Illumina [149310] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176756 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13745) 2,466 Black/admixed ancestry individuals NA Illumina [151556] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176757 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13749) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150870] 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176758 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1376) 2,466 Black/admixed ancestry individuals NA Illumina [171128] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176759 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13769) 2,466 Black/admixed ancestry individuals NA Illumina [161535] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176760 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1377) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161078] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176761 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13770) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161814] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176762 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13773) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152972] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176763 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13785) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152080] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176764 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13917) 2,466 Black/admixed ancestry individuals NA Illumina [145584] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176787 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13919) 2,466 Black/admixed ancestry individuals NA Illumina [184758] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178985 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13920) 2,466 Black/admixed ancestry individuals NA Illumina [145334] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176788 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13924) 2,466 Black/admixed ancestry individuals NA Illumina [154607] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176789 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13928) 2,466 Black/admixed ancestry individuals NA Illumina [166872] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176790 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13936) 2,466 Black/admixed ancestry individuals NA Illumina [279773] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178986 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13938) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154731] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176791 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13939) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153953] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176792 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1395) 2,466 Black/admixed ancestry individuals NA Illumina [143694] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176793 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13951) 2,466 Black/admixed ancestry individuals NA Illumina [161702] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176794 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13953) 2,466 Black/admixed ancestry individuals NA Illumina [160864] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176795 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13954) 2,466 Black/admixed ancestry individuals NA Illumina [154611] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176796 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13959) 2,466 Black/admixed ancestry individuals NA Illumina [134594] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176797 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1396) 2,466 Black/admixed ancestry individuals NA Illumina [155757] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176798 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13964) 2,466 Black/admixed ancestry individuals NA Illumina [139741] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176799 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13969) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [171904] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176800 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1397) 2,466 Black/admixed ancestry individuals NA Illumina [159388] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176801 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13970) 2,466 Black/admixed ancestry individuals NA Illumina [152428] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176802 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13972) 2,466 Black/admixed ancestry individuals NA Illumina [149226] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176803 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13974) 2,466 Black/admixed ancestry individuals NA Illumina [152541] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176804 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13975) 2,466 Black/admixed ancestry individuals NA Illumina [166703] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176805 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13976) 2,466 Black/admixed ancestry individuals NA Illumina [176738] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176806 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13988) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [175857] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176807 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13997) 2,466 Black/admixed ancestry individuals NA Illumina [147194] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176808 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13997) 2,466 Black/admixed ancestry individuals NA Illumina [150671] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178765 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14005) 2,466 Black/admixed ancestry individuals NA Illumina [173272] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176809 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14009) 2,466 Black/admixed ancestry individuals NA Illumina [159281] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176810 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1401) 2,466 Black/admixed ancestry individuals NA Illumina [160474] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176811 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14010) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148291] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176812 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14012) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155913] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176813 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14015) 2,466 Black/admixed ancestry individuals NA Illumina [170395] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176814 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14018) 2,466 Black/admixed ancestry individuals NA Illumina [155322] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178987 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14027) 2,466 Black/admixed ancestry individuals NA Illumina [155442] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178988 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14029) 2,466 Black/admixed ancestry individuals NA Illumina [147991] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176815 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14029) 2,466 Black/admixed ancestry individuals NA Illumina [136237] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178989 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14032) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [147759] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176816 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14034) 2,466 Black/admixed ancestry individuals NA Illumina [151237] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176817 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14035) 2,466 Black/admixed ancestry individuals NA Illumina [161910] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176818 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14035) 2,466 Black/admixed ancestry individuals NA Illumina [152654] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178990 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14045) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150160] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176819 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14053) 2,466 Black/admixed ancestry individuals NA Illumina [150546] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176820 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14053) 2,466 Black/admixed ancestry individuals NA Illumina [151095] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178766 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14055) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152968] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176821 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14061) 2,466 Black/admixed ancestry individuals NA Illumina [151328] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176822 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14061) 2,466 Black/admixed ancestry individuals NA Illumina [170043] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178991 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14070) 2,466 Black/admixed ancestry individuals NA Illumina [167068] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176823 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14085) 2,466 Black/admixed ancestry individuals NA Illumina [179625] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176824 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14087) 2,466 Black/admixed ancestry individuals NA Illumina [153365] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176825 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14095) 2,466 Black/admixed ancestry individuals NA Illumina [153017] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176826 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14102) 2,466 Black/admixed ancestry individuals NA Illumina [154374] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176827 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6512) 2,466 Black/admixed ancestry individuals NA Illumina [153467] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178132 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6513) 2,466 Black/admixed ancestry individuals NA Illumina [166527] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178133 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6521) 2,466 Black/admixed ancestry individuals NA Illumina [148200] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178134 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6521) 2,466 Black/admixed ancestry individuals NA Illumina [147204] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178888 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6523) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150886] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178135 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6525) 2,466 Black/admixed ancestry individuals NA Illumina [150644] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178136 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI654) 2,466 Black/admixed ancestry individuals NA Illumina [152586] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178137 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6545) 2,466 Black/admixed ancestry individuals NA Illumina [183871] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179085 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI655) 2,466 Black/admixed ancestry individuals NA Illumina [154121] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178138 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6556) 2,466 Black/admixed ancestry individuals NA Illumina [148850] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178139 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6558) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153051] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178140 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI656) 2,466 Black/admixed ancestry individuals NA Illumina [153588] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178141 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6567) 2,466 Black/admixed ancestry individuals NA Illumina [169529] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178142 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6568) 2,466 Black/admixed ancestry individuals NA Illumina [143153] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178143 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6570) 2,466 Black/admixed ancestry individuals NA Illumina [153379] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178144 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6578) 2,466 Black/admixed ancestry individuals NA Illumina [150941] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178145 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6580) 2,466 Black/admixed ancestry individuals NA Illumina [139946] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178146 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6580) 2,466 Black/admixed ancestry individuals NA Illumina [145306] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178889 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6598) 2,466 Black/admixed ancestry individuals NA Illumina [171032] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178147 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6599) 2,466 Black/admixed ancestry individuals NA Illumina [152663] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178148 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI660) 2,466 Black/admixed ancestry individuals NA Illumina [153046] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178149 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6604) 2,466 Black/admixed ancestry individuals NA Illumina [147066] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178150 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI661) 2,466 Black/admixed ancestry individuals NA Illumina [157524] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178151 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6616) 2,466 Black/admixed ancestry individuals NA Illumina [156976] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178152 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6617) 2,466 Black/admixed ancestry individuals NA Illumina [155866] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178153 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1379) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148628] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176765 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1379) 2,466 Black/admixed ancestry individuals NA Illumina [150241] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178763 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13792) 2,466 Black/admixed ancestry individuals NA Illumina [158764] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176766 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13798) 2,466 Black/admixed ancestry individuals NA Illumina [157438] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176767 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13820) 2,466 Black/admixed ancestry individuals NA Illumina [153926] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176768 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13820) 2,466 Black/admixed ancestry individuals NA Illumina [149662] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178984 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13829) 2,466 Black/admixed ancestry individuals NA Illumina [154577] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176769 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13830) 2,466 Black/admixed ancestry individuals NA Illumina [148409] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176770 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13840) 2,466 Black/admixed ancestry individuals NA Illumina [155873] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176771 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13840) 2,466 Black/admixed ancestry individuals NA Illumina [170182] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178764 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13853) 2,466 Black/admixed ancestry individuals NA Illumina [156795] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176772 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13856) 2,466 Black/admixed ancestry individuals NA Illumina [154171] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176773 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13859) 2,466 Black/admixed ancestry individuals NA Illumina [150875] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176774 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13869) 2,466 Black/admixed ancestry individuals NA Illumina [162104] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176775 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13878) 2,466 Black/admixed ancestry individuals NA Illumina [157124] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176776 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13885) 2,466 Black/admixed ancestry individuals NA Illumina [147651] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176777 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13887) 2,466 Black/admixed ancestry individuals NA Illumina [149143] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176778 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13888) 2,466 Black/admixed ancestry individuals NA Illumina [152803] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176779 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13898) 2,466 Black/admixed ancestry individuals NA Illumina [164967] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176780 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13900) 2,466 Black/admixed ancestry individuals NA Illumina [148845] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176781 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13902) 2,466 Black/admixed ancestry individuals NA Illumina [152369] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176782 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1391) 2,466 Black/admixed ancestry individuals NA Illumina [161095] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176783 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13911) 2,466 Black/admixed ancestry individuals NA Illumina [130834] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176784 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13912) 2,466 Black/admixed ancestry individuals NA Illumina [177979] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176785 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI13913) 2,466 Black/admixed ancestry individuals NA Illumina [142746] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176786 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6618) 2,466 Black/admixed ancestry individuals NA Illumina [150421] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178154 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6626) 2,466 Black/admixed ancestry individuals NA Illumina [156309] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178155 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI663) 2,466 Black/admixed ancestry individuals NA Illumina [164065] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178156 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6634) 2,466 Black/admixed ancestry individuals NA Illumina [152177] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178157 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6635) 2,466 Black/admixed ancestry individuals NA Illumina [152836] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178158 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6636) 2,466 Black/admixed ancestry individuals NA Illumina [149974] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178159 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6641) 2,466 Black/admixed ancestry individuals NA Illumina [159010] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178160 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6645) 2,466 Black/admixed ancestry individuals NA Illumina [148717] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178161 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6650) 2,466 Black/admixed ancestry individuals NA Illumina [155538] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178162 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6655) 2,466 Black/admixed ancestry individuals NA Illumina [169429] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178163 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6656) 2,466 Black/admixed ancestry individuals NA Illumina [156641] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178164 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6657) 2,466 Black/admixed ancestry individuals NA Illumina [161308] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178165 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6658) 2,466 Black/admixed ancestry individuals NA Illumina [155589] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178166 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6659) 2,466 Black/admixed ancestry individuals NA Illumina [157783] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178167 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6660) 2,466 Black/admixed ancestry individuals NA Illumina [148843] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178168 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6661) 2,466 Black/admixed ancestry individuals NA Illumina [152794] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178169 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6662) 2,466 Black/admixed ancestry individuals NA Illumina [155198] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178170 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6663) 2,466 Black/admixed ancestry individuals NA Illumina [149637] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178171 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6664) 2,466 Black/admixed ancestry individuals NA Illumina [156813] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178172 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6665) 2,466 Black/admixed ancestry individuals NA Illumina [154509] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178173 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6666) 2,466 Black/admixed ancestry individuals NA Illumina [158058] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178174 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6667) 2,466 Black/admixed ancestry individuals NA Illumina [146890] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178175 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6668) 2,466 Black/admixed ancestry individuals NA Illumina [163357] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178176 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6669) 2,466 Black/admixed ancestry individuals NA Illumina [164838] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178177 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6670) 2,466 Black/admixed ancestry individuals NA Illumina [167143] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178178 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI744) 2,466 Black/admixed ancestry individuals NA Illumina [148828] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178347 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7444) 2,466 Black/admixed ancestry individuals NA Illumina [147485] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178348 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7452) 2,466 Black/admixed ancestry individuals NA Illumina [154238] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178349 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7462) 2,466 Black/admixed ancestry individuals NA Illumina [163222] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178350 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7462) 2,466 Black/admixed ancestry individuals NA Illumina [158371] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179089 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7471) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149055] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178351 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7471) 2,466 Black/admixed ancestry individuals NA Illumina [151925] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178901 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI748) 2,466 Black/admixed ancestry individuals NA Illumina [151757] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178352 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI748) 2,466 Black/admixed ancestry individuals NA Illumina [144396] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178902 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7489) 2,466 Black/admixed ancestry individuals NA Illumina [151930] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178353 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI750) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150546] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178354 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7520) 2,466 Black/admixed ancestry individuals NA Illumina [160081] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178355 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7549) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156604] 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178356 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI757) 2,466 Black/admixed ancestry individuals NA Illumina [152802] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178357 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI758) 2,466 Black/admixed ancestry individuals NA Illumina [155022] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178358 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7601) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159997] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178359 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI762) 2,466 Black/admixed ancestry individuals NA Illumina [153745] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178360 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7633) 2,466 Black/admixed ancestry individuals NA Illumina [154409] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178361 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7638) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149657] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178362 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7653) 2,466 Black/admixed ancestry individuals NA Illumina [153752] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178363 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7673) 2,466 Black/admixed ancestry individuals NA Illumina [157123] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178364 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7674) 2,466 Black/admixed ancestry individuals NA Illumina [150090] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178365 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7703) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153410] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178366 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI775) 2,466 Black/admixed ancestry individuals NA Illumina [154492] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178367 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI776) 2,466 Black/admixed ancestry individuals NA Illumina [150952] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178368 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7319) 2,466 Black/admixed ancestry individuals NA Illumina [142530] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179087 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7335) 2,466 Black/admixed ancestry individuals NA Illumina [149818] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178325 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7337) 2,466 Black/admixed ancestry individuals NA Illumina [152764] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178326 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7338) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152741] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178327 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7339) 2,466 Black/admixed ancestry individuals NA Illumina [151018] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178328 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI735) 2,466 Black/admixed ancestry individuals NA Illumina [153448] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178329 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7354) 2,466 Black/admixed ancestry individuals NA Illumina [153723] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178330 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7372) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [165871] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178331 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7379) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153313] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178332 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7380) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155752] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178333 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7387) 2,466 Black/admixed ancestry individuals NA Illumina [152259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178334 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7388) 2,466 Black/admixed ancestry individuals NA Illumina [138453] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178335 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7389) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [209949] 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178336 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI739) 2,466 Black/admixed ancestry individuals NA Illumina [166339] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178337 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7401) 2,466 Black/admixed ancestry individuals NA Illumina [149450] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178338 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7403) 2,466 Black/admixed ancestry individuals NA Illumina [154043] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178339 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7406) 2,466 Black/admixed ancestry individuals NA Illumina [146292] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178340 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7406) 2,466 Black/admixed ancestry individuals NA Illumina [150766] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178900 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7407) 2,466 Black/admixed ancestry individuals NA Illumina [146991] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178341 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7407) 2,466 Black/admixed ancestry individuals NA Illumina [149044] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179088 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7417) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157713] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178342 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7429) 2,466 Black/admixed ancestry individuals NA Illumina [160036] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178343 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7430) 2,466 Black/admixed ancestry individuals NA Illumina [154548] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178344 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7434) 2,466 Black/admixed ancestry individuals NA Illumina [148955] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178345 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7438) 2,466 Black/admixed ancestry individuals NA Illumina [150174] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178346 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14552) 2,466 Black/admixed ancestry individuals NA Illumina [154564] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176895 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14554) 2,466 Black/admixed ancestry individuals NA Illumina [157169] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176896 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14556) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154627] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176897 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14558) 2,466 Black/admixed ancestry individuals NA Illumina [155025] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176898 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14558) 2,466 Black/admixed ancestry individuals NA Illumina [150375] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178997 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14560) 2,466 Black/admixed ancestry individuals NA Illumina [167861] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176899 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14561) 2,466 Black/admixed ancestry individuals NA Illumina [148685] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176900 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14561) 2,466 Black/admixed ancestry individuals NA Illumina [145249] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178778 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14562) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154235] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176901 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14564) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155201] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176902 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14567) 2,466 Black/admixed ancestry individuals NA Illumina [149946] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176903 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14568) 2,466 Black/admixed ancestry individuals NA Illumina [151084] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176904 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14568) 2,466 Black/admixed ancestry individuals NA Illumina [151529] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178779 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14569) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156258] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176905 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1457) 2,466 Black/admixed ancestry individuals NA Illumina [152804] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176906 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14570) 2,466 Black/admixed ancestry individuals NA Illumina [151069] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176907 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI712) 2,466 Black/admixed ancestry individuals NA Illumina [157367] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178896 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7121) 2,466 Black/admixed ancestry individuals NA Illumina [158467] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178295 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7122) 2,466 Black/admixed ancestry individuals NA Illumina [153261] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178296 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7136) 2,466 Black/admixed ancestry individuals NA Illumina [150176] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178297 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7137) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150573] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178298 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7156) 2,466 Black/admixed ancestry individuals NA Illumina [158294] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178299 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7161) 2,466 Black/admixed ancestry individuals NA Illumina [164925] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178300 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7187) 2,466 Black/admixed ancestry individuals NA Illumina [155066] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178301 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7191) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156528] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178302 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI720) 2,466 Black/admixed ancestry individuals NA Illumina [153244] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178303 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7211) 2,466 Black/admixed ancestry individuals NA Illumina [155416] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178304 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7214) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [179845] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178305 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI722) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151947] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178306 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7226) 2,466 Black/admixed ancestry individuals NA Illumina [152084] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178307 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7226) 2,466 Black/admixed ancestry individuals NA Illumina [155365] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178897 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7228) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [164574] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178308 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI723) 2,466 Black/admixed ancestry individuals NA Illumina [153724] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178309 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7232) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155356] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178310 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7241) 2,466 Black/admixed ancestry individuals NA Illumina [154918] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178311 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7241) 2,466 Black/admixed ancestry individuals NA Illumina [156000] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178898 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7248) 2,466 Black/admixed ancestry individuals NA Illumina [151932] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178312 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7248) 2,466 Black/admixed ancestry individuals NA Illumina [163004] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178899 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7253) 2,466 Black/admixed ancestry individuals NA Illumina [172239] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178313 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7255) 2,466 Black/admixed ancestry individuals NA Illumina [153451] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178314 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI726) 2,466 Black/admixed ancestry individuals NA Illumina [152899] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178315 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7262) 2,466 Black/admixed ancestry individuals NA Illumina [152806] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178316 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7267) 2,466 Black/admixed ancestry individuals NA Illumina [151525] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178317 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7269) 2,466 Black/admixed ancestry individuals NA Illumina [158049] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178318 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI727) 2,466 Black/admixed ancestry individuals NA Illumina [154005] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178319 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7277) 2,466 Black/admixed ancestry individuals NA Illumina [154359] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178320 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7282) 2,466 Black/admixed ancestry individuals NA Illumina [153599] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178321 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7299) 2,466 Black/admixed ancestry individuals NA Illumina [149261] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178322 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7312) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153122] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178323 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7319) 2,466 Black/admixed ancestry individuals NA Illumina [145422] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178324 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI7771) 2,466 Black/admixed ancestry individuals NA Illumina [1368818] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178369 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI784) 2,466 Black/admixed ancestry individuals NA Illumina [152081] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178370 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI787) 2,466 Black/admixed ancestry individuals NA Illumina [148092] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178371 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI787) 2,466 Black/admixed ancestry individuals NA Illumina [149333] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178903 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI790) 2,466 Black/admixed ancestry individuals NA Illumina [152682] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178372 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI791) 2,466 Black/admixed ancestry individuals NA Illumina [156090] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178373 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI794) 2,466 Black/admixed ancestry individuals NA Illumina [379264] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179090 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI797) 2,466 Black/admixed ancestry individuals NA Illumina [151719] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178374 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI799) 2,466 Black/admixed ancestry individuals NA Illumina [150503] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178375 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI8) 2,466 Black/admixed ancestry individuals NA Illumina [171089] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178376 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14572) 2,466 Black/admixed ancestry individuals NA Illumina [150512] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176908 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14572) 2,466 Black/admixed ancestry individuals NA Illumina [169112] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178998 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1459) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153910] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176909 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14601) 2,466 Black/admixed ancestry individuals NA Illumina [153533] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176910 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14603) 2,466 Black/admixed ancestry individuals NA Illumina [150353] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176911 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14603) 2,466 Black/admixed ancestry individuals NA Illumina [169592] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178780 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14606) 2,466 Black/admixed ancestry individuals NA Illumina [149069] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176912 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14611) 2,466 Black/admixed ancestry individuals NA Illumina [140625] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176913 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14614) 2,466 Black/admixed ancestry individuals NA Illumina [153941] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176914 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14615) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [144162] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176915 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14616) 2,466 Black/admixed ancestry individuals NA Illumina [144242] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176916 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14617) 2,466 Black/admixed ancestry individuals NA Illumina [150004] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176917 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14617) 2,466 Black/admixed ancestry individuals NA Illumina [162589] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178999 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14618) 2,466 Black/admixed ancestry individuals NA Illumina [153457] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176918 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14620) 2,466 Black/admixed ancestry individuals NA Illumina [160533] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176919 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14621) 2,466 Black/admixed ancestry individuals NA Illumina [151176] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176920 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14622) 2,466 Black/admixed ancestry individuals NA Illumina [161788] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176921 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14625) 2,466 Black/admixed ancestry individuals NA Illumina [170882] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176922 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14627) 2,466 Black/admixed ancestry individuals NA Illumina [155110] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176923 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14628) 2,466 Black/admixed ancestry individuals NA Illumina [171601] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176924 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14638) 2,466 Black/admixed ancestry individuals NA Illumina [153762] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176925 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14641) 2,466 Black/admixed ancestry individuals NA Illumina [155617] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176926 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14643) 2,466 Black/admixed ancestry individuals NA Illumina [159782] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176927 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14644) 2,466 Black/admixed ancestry individuals NA Illumina [164146] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176928 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14656) 2,466 Black/admixed ancestry individuals NA Illumina [140233] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176929 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14660) 2,466 Black/admixed ancestry individuals NA Illumina [149145] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176930 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14665) 2,466 Black/admixed ancestry individuals NA Illumina [166533] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176931 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14666) 2,466 Black/admixed ancestry individuals NA Illumina [161337] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176932 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14668) 2,466 Black/admixed ancestry individuals NA Illumina [152842] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176933 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14668) 2,466 Black/admixed ancestry individuals NA Illumina [156813] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178781 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14671) 2,466 Black/admixed ancestry individuals NA Illumina [167464] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176934 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14675) 2,466 Black/admixed ancestry individuals NA Illumina [153405] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176935 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14675) 2,466 Black/admixed ancestry individuals NA Illumina [149932] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178782 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14686) 2,466 Black/admixed ancestry individuals NA Illumina [156808] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176936 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14703) 2,466 Black/admixed ancestry individuals NA Illumina [158916] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176937 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14704) 2,466 Black/admixed ancestry individuals NA Illumina [153211] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176938 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14706) 2,466 Black/admixed ancestry individuals NA Illumina [147287] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176939 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14707) 2,466 Black/admixed ancestry individuals NA Illumina [156214] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176940 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14709) 2,466 Black/admixed ancestry individuals NA Illumina [151256] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176941 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI14711) 2,466 Black/admixed ancestry individuals NA Illumina [157068] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176942 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15290) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152000] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177075 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15293) 2,466 Black/admixed ancestry individuals NA Illumina [164349] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177076 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15293) 2,466 Black/admixed ancestry individuals NA Illumina [145901] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179010 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI910) 2,466 Black/admixed ancestry individuals NA Illumina [164744] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178462 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI910) 2,466 Black/admixed ancestry individuals NA Illumina [172727] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179094 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9103) 2,466 Black/admixed ancestry individuals NA Illumina [151855] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178463 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9110) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158935] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178464 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9111) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [175003] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178465 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9112) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155910] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178466 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9113) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [163821] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178467 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9119) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [166717] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178468 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI912) 2,466 Black/admixed ancestry individuals NA Illumina [153050] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178469 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9134) 2,466 Black/admixed ancestry individuals NA Illumina [145115] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178470 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9142) 2,466 Black/admixed ancestry individuals NA Illumina [156426] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178471 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9183) 2,466 Black/admixed ancestry individuals NA Illumina [155254] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178472 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9192) 2,466 Black/admixed ancestry individuals NA Illumina [146559] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178473 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9201) 2,466 Black/admixed ancestry individuals NA Illumina [148780] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178474 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9202) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153925] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178475 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9210) 2,466 Black/admixed ancestry individuals NA Illumina [152634] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178476 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9211) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161106] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178477 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9214) 2,466 Black/admixed ancestry individuals NA Illumina [166196] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178478 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI923) 2,466 Black/admixed ancestry individuals NA Illumina [155790] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178479 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9231) 2,466 Black/admixed ancestry individuals NA Illumina [170198] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178480 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9235) 2,466 Black/admixed ancestry individuals NA Illumina [153278] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178481 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI924) 2,466 Black/admixed ancestry individuals NA Illumina [154080] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178482 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9376) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158420] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178506 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9378) 2,466 Black/admixed ancestry individuals NA Illumina [162852] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178507 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9382) 2,466 Black/admixed ancestry individuals NA Illumina [155165] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178508 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9384) 2,466 Black/admixed ancestry individuals NA Illumina [153846] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178509 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9384) 2,466 Black/admixed ancestry individuals NA Illumina [169719] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178911 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9385) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150988] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178510 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9388) 2,466 Black/admixed ancestry individuals NA Illumina [156613] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178511 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9388) 2,466 Black/admixed ancestry individuals NA Illumina [162351] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178912 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9389) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155038] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178512 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9399) 2,466 Black/admixed ancestry individuals NA Illumina [152138] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178513 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9413) 2,466 Black/admixed ancestry individuals NA Illumina [160392] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178514 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9425) 2,466 Black/admixed ancestry individuals NA Illumina [154260] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178515 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9427) 2,466 Black/admixed ancestry individuals NA Illumina [159838] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178516 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9431) 2,466 Black/admixed ancestry individuals NA Illumina [158582] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178517 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9432) 2,466 Black/admixed ancestry individuals NA Illumina [167405] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178518 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9439) 2,466 Black/admixed ancestry individuals NA Illumina [156755] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178519 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI944) 2,466 Black/admixed ancestry individuals NA Illumina [154746] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178520 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9441) 2,466 Black/admixed ancestry individuals NA Illumina [162938] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178521 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9444) 2,466 Black/admixed ancestry individuals NA Illumina [154960] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178522 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9445) 2,466 Black/admixed ancestry individuals NA Illumina [154048] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178523 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9448) 2,466 Black/admixed ancestry individuals NA Illumina [150024] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178524 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9449) 2,466 Black/admixed ancestry individuals NA Illumina [153651] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178525 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI945) 2,466 Black/admixed ancestry individuals NA Illumina [156687] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178526 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9451) 2,466 Black/admixed ancestry individuals NA Illumina [155579] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178527 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9452) 2,466 Black/admixed ancestry individuals NA Illumina [152913] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178528 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI925) 2,466 Black/admixed ancestry individuals NA Illumina [154538] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178483 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI927) 2,466 Black/admixed ancestry individuals NA Illumina [168061] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178484 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI927) 2,466 Black/admixed ancestry individuals NA Illumina [141348] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179095 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9278) 2,466 Black/admixed ancestry individuals NA Illumina [164076] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178485 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9279) 2,466 Black/admixed ancestry individuals NA Illumina [150439] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178486 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9282) 2,466 Black/admixed ancestry individuals NA Illumina [148957] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178487 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9286) 2,466 Black/admixed ancestry individuals NA Illumina [152081] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178488 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9288) 2,466 Black/admixed ancestry individuals NA Illumina [151806] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178489 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9289) 2,466 Black/admixed ancestry individuals NA Illumina [152012] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178490 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9290) 2,466 Black/admixed ancestry individuals NA Illumina [147921] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178491 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9291) 2,466 Black/admixed ancestry individuals NA Illumina [149179] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178492 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9292) 2,466 Black/admixed ancestry individuals NA Illumina [153229] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178493 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9293) 2,466 Black/admixed ancestry individuals NA Illumina [148402] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178494 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9295) 2,466 Black/admixed ancestry individuals NA Illumina [152505] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178495 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9297) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [194425] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178496 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9299) 2,466 Black/admixed ancestry individuals NA Illumina [157741] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178497 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9307) 2,466 Black/admixed ancestry individuals NA Illumina [161613] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178498 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9315) 2,466 Black/admixed ancestry individuals NA Illumina [165328] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178499 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9330) 2,466 Black/admixed ancestry individuals NA Illumina [151146] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178500 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9336) 2,466 Black/admixed ancestry individuals NA Illumina [154717] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178501 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9343) 2,466 Black/admixed ancestry individuals NA Illumina [158345] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178502 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9343) 2,466 Black/admixed ancestry individuals NA Illumina [159088] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179096 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9365) 2,466 Black/admixed ancestry individuals NA Illumina [162931] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178503 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9368) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151558] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178504 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9369) 2,466 Black/admixed ancestry individuals NA Illumina [162397] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178505 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15224) 2,466 Black/admixed ancestry individuals NA Illumina [162402] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177052 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15225) 2,466 Black/admixed ancestry individuals NA Illumina [150882] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177053 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15229) 2,466 Black/admixed ancestry individuals NA Illumina [170022] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177054 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15229) 2,466 Black/admixed ancestry individuals NA Illumina [166134] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178796 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15232) 2,466 Black/admixed ancestry individuals NA Illumina [153734] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177055 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15233) 2,466 Black/admixed ancestry individuals NA Illumina [152171] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177056 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15234) 2,466 Black/admixed ancestry individuals NA Illumina [152951] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177057 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15235) 2,466 Black/admixed ancestry individuals NA Illumina [154334] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177058 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15243) 2,466 Black/admixed ancestry individuals NA Illumina [145371] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177059 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15249) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152831] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177060 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1525) 2,466 Black/admixed ancestry individuals NA Illumina [141668] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177061 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15251) 2,466 Black/admixed ancestry individuals NA Illumina [149142] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177062 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15251) 2,466 Black/admixed ancestry individuals NA Illumina [133044] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179009 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15256) 2,466 Black/admixed ancestry individuals NA Illumina [132302] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177063 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15260) 2,466 Black/admixed ancestry individuals NA Illumina [151234] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177064 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15262) 2,466 Black/admixed ancestry individuals NA Illumina [156724] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177065 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15268) 2,466 Black/admixed ancestry individuals NA Illumina [152646] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177066 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15269) 2,466 Black/admixed ancestry individuals NA Illumina [154932] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177067 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15270) 2,466 Black/admixed ancestry individuals NA Illumina [153025] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177068 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15271) 2,466 Black/admixed ancestry individuals NA Illumina [154261] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177069 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1528) 2,466 Black/admixed ancestry individuals NA Illumina [153023] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177070 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15280) 2,466 Black/admixed ancestry individuals NA Illumina [151085] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177071 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15281) 2,466 Black/admixed ancestry individuals NA Illumina [152664] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177072 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15288) 2,466 Black/admixed ancestry individuals NA Illumina [160180] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177073 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1529) 2,466 Black/admixed ancestry individuals NA Illumina [151802] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177074 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9455) 2,466 Black/admixed ancestry individuals NA Illumina [156383] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178529 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9457) 2,466 Black/admixed ancestry individuals NA Illumina [153579] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178530 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9459) 2,466 Black/admixed ancestry individuals NA Illumina [151632] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178531 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9464) 2,466 Black/admixed ancestry individuals NA Illumina [151732] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178532 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9469) 2,466 Black/admixed ancestry individuals NA Illumina [151852] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178533 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9472) 2,466 Black/admixed ancestry individuals NA Illumina [158959] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178534 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9475) 2,466 Black/admixed ancestry individuals NA Illumina [172399] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178535 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9479) 2,466 Black/admixed ancestry individuals NA Illumina [153842] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178536 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9480) 2,466 Black/admixed ancestry individuals NA Illumina [157758] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178537 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9482) 2,466 Black/admixed ancestry individuals NA Illumina [153437] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178538 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15295) 2,466 Black/admixed ancestry individuals NA Illumina [153833] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177077 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15295) 2,466 Black/admixed ancestry individuals NA Illumina [143625] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179011 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15296) 2,466 Black/admixed ancestry individuals NA Illumina [157382] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177078 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1530) 2,466 Black/admixed ancestry individuals NA Illumina [160720] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177079 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15301) 2,466 Black/admixed ancestry individuals NA Illumina [159469] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177080 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15303) 2,466 Black/admixed ancestry individuals NA Illumina [146641] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177081 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15309) 2,466 Black/admixed ancestry individuals NA Illumina [165962] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177082 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15309) 2,466 Black/admixed ancestry individuals NA Illumina [151894] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178797 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15312) 2,466 Black/admixed ancestry individuals NA Illumina [150252] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177083 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15315) 2,466 Black/admixed ancestry individuals NA Illumina [164145] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177084 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15318) 2,466 Black/admixed ancestry individuals NA Illumina [155101] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177085 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15318) 2,466 Black/admixed ancestry individuals NA Illumina [154622] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178798 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15320) 2,466 Black/admixed ancestry individuals NA Illumina [163805] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177086 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15324) 2,466 Black/admixed ancestry individuals NA Illumina [151220] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177087 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15331) 2,466 Black/admixed ancestry individuals NA Illumina [147753] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177088 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15101) 2,466 Black/admixed ancestry individuals NA Illumina [147847] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177029 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15106) 2,466 Black/admixed ancestry individuals NA Illumina [154282] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177030 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15133) 2,466 Black/admixed ancestry individuals NA Illumina [161338] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177031 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15137) 2,466 Black/admixed ancestry individuals NA Illumina [149007] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177032 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15140) 2,466 Black/admixed ancestry individuals NA Illumina [153366] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177033 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15152) 2,466 Black/admixed ancestry individuals NA Illumina [158540] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177034 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15153) 2,466 Black/admixed ancestry individuals NA Illumina [153260] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177035 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15154) 2,466 Black/admixed ancestry individuals NA Illumina [167332] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177036 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15154) 2,466 Black/admixed ancestry individuals NA Illumina [150086] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178794 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15167) 2,466 Black/admixed ancestry individuals NA Illumina [152250] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177037 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15168) 2,466 Black/admixed ancestry individuals NA Illumina [150126] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177038 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15169) 2,466 Black/admixed ancestry individuals NA Illumina [155658] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177039 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15171) 2,466 Black/admixed ancestry individuals NA Illumina [151349] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177040 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15182) 2,466 Black/admixed ancestry individuals NA Illumina [153990] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177041 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15183) 2,466 Black/admixed ancestry individuals NA Illumina [171798] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177042 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15183) 2,466 Black/admixed ancestry individuals NA Illumina [169853] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178795 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15189) 2,466 Black/admixed ancestry individuals NA Illumina [157301] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177043 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15197) 2,466 Black/admixed ancestry individuals NA Illumina [144873] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177044 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15205) 2,466 Black/admixed ancestry individuals NA Illumina [154590] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177045 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1521) 2,466 Black/admixed ancestry individuals NA Illumina [155902] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177046 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15210) 2,466 Black/admixed ancestry individuals NA Illumina [166032] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177047 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15211) 2,466 Black/admixed ancestry individuals NA Illumina [156730] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177048 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1522) 2,466 Black/admixed ancestry individuals NA Illumina [163873] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177049 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15221) 2,466 Black/admixed ancestry individuals NA Illumina [159999] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177050 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15223) 2,466 Black/admixed ancestry individuals NA Illumina [149062] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177051 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15002) 2,466 Black/admixed ancestry individuals NA Illumina [152617] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177009 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15004) 2,466 Black/admixed ancestry individuals NA Illumina [165148] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177010 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15005) 2,466 Black/admixed ancestry individuals NA Illumina [154438] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177011 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15007) 2,466 Black/admixed ancestry individuals NA Illumina [140592] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177012 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15014) 2,466 Black/admixed ancestry individuals NA Illumina [155164] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177013 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15020) 2,466 Black/admixed ancestry individuals NA Illumina [152663] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177014 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15021) 2,466 Black/admixed ancestry individuals NA Illumina [146345] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177015 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15021) 2,466 Black/admixed ancestry individuals NA Illumina [160420] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179004 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15022) 2,466 Black/admixed ancestry individuals NA Illumina [166673] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177016 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15027) 2,466 Black/admixed ancestry individuals NA Illumina [159876] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177017 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15037) 2,466 Black/admixed ancestry individuals NA Illumina [152801] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177018 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15049) 2,466 Black/admixed ancestry individuals NA Illumina [150320] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177019 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1506) 2,466 Black/admixed ancestry individuals NA Illumina [165720] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177020 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15074) 2,466 Black/admixed ancestry individuals NA Illumina [153404] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177021 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15074) 2,466 Black/admixed ancestry individuals NA Illumina [140884] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179005 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15077) 2,466 Black/admixed ancestry individuals NA Illumina [170552] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179006 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15094) 2,466 Black/admixed ancestry individuals NA Illumina [152102] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177023 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15094) 2,466 Black/admixed ancestry individuals NA Illumina [154841] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179007 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15096) 2,466 Black/admixed ancestry individuals NA Illumina [148935] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177024 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15097) 2,466 Black/admixed ancestry individuals NA Illumina [148963] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177025 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15097) 2,466 Black/admixed ancestry individuals NA Illumina [165727] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178793 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15098) 2,466 Black/admixed ancestry individuals NA Illumina [153604] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177026 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15098) 2,466 Black/admixed ancestry individuals NA Illumina [154672] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179008 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15099) 2,466 Black/admixed ancestry individuals NA Illumina [161742] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177027 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15100) 2,466 Black/admixed ancestry individuals NA Illumina [148594] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177028 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI960) 2,466 Black/admixed ancestry individuals NA Illumina [159149] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178590 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9607) 2,466 Black/admixed ancestry individuals NA Illumina [161308] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178591 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI961) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153034] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178592 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9610) 2,466 Black/admixed ancestry individuals NA Illumina [153037] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178593 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9625) 2,466 Black/admixed ancestry individuals NA Illumina [155544] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178594 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9632) 2,466 Black/admixed ancestry individuals NA Illumina [165238] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178595 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9643) 2,466 Black/admixed ancestry individuals NA Illumina [150817] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178596 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9643) 2,466 Black/admixed ancestry individuals NA Illumina [173735] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179097 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9645) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157931] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178597 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9523) 2,466 Black/admixed ancestry individuals NA Illumina [165471] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178562 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9524) 2,466 Black/admixed ancestry individuals NA Illumina [165457] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178563 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9525) 2,466 Black/admixed ancestry individuals NA Illumina [165630] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178564 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9528) 2,466 Black/admixed ancestry individuals NA Illumina [150740] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178565 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9529) 2,466 Black/admixed ancestry individuals NA Illumina [168163] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178566 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9530) 2,466 Black/admixed ancestry individuals NA Illumina [158177] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178567 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9531) 2,466 Black/admixed ancestry individuals NA Illumina [157751] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178568 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9533) 2,466 Black/admixed ancestry individuals NA Illumina [155195] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178569 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9534) 2,466 Black/admixed ancestry individuals NA Illumina [165678] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178570 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9536) 2,466 Black/admixed ancestry individuals NA Illumina [151490] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178571 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9537) 2,466 Black/admixed ancestry individuals NA Illumina [154650] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178572 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9541) 2,466 Black/admixed ancestry individuals NA Illumina [150609] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178573 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9542) 2,466 Black/admixed ancestry individuals NA Illumina [164599] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178574 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9543) 2,466 Black/admixed ancestry individuals NA Illumina [158705] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178575 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9544) 2,466 Black/admixed ancestry individuals NA Illumina [157846] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178576 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9546) 2,466 Black/admixed ancestry individuals NA Illumina [153842] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178577 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9548) 2,466 Black/admixed ancestry individuals NA Illumina [157747] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178578 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9549) 2,466 Black/admixed ancestry individuals NA Illumina [157468] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178579 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9552) 2,466 Black/admixed ancestry individuals NA Illumina [155082] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178580 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9553) 2,466 Black/admixed ancestry individuals NA Illumina [154095] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178581 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9557) 2,466 Black/admixed ancestry individuals NA Illumina [154777] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178582 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9558) 2,466 Black/admixed ancestry individuals NA Illumina [158739] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178583 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9566) 2,466 Black/admixed ancestry individuals NA Illumina [160922] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178584 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9568) 2,466 Black/admixed ancestry individuals NA Illumina [168057] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178585 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9575) 2,466 Black/admixed ancestry individuals NA Illumina [155664] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178586 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI958) 2,466 Black/admixed ancestry individuals NA Illumina [155915] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178587 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI959) 2,466 Black/admixed ancestry individuals NA Illumina [155902] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178588 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9590) 2,466 Black/admixed ancestry individuals NA Illumina [152032] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178589 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9655) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156651] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178598 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9668) 2,466 Black/admixed ancestry individuals NA Illumina [148246] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178599 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9671) 2,466 Black/admixed ancestry individuals NA Illumina [158741] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178600 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9672) 2,466 Black/admixed ancestry individuals NA Illumina [157087] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178601 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9677) 2,466 Black/admixed ancestry individuals NA Illumina [162470] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178602 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9680) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [204487] 6 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178603 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9684) 2,466 Black/admixed ancestry individuals NA Illumina [169034] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178604 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9685) 2,466 Black/admixed ancestry individuals NA Illumina [150862] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178605 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI969) 2,466 Black/admixed ancestry individuals NA Illumina [170377] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179098 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9693) 2,466 Black/admixed ancestry individuals NA Illumina [150703] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178606 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9694) 2,466 Black/admixed ancestry individuals NA Illumina [154590] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178607 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9698) 2,466 Black/admixed ancestry individuals NA Illumina [148698] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178608 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9699) 2,466 Black/admixed ancestry individuals NA Illumina [151666] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178609 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1715) 2,466 Black/admixed ancestry individuals NA Illumina [145386] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177389 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1715) 2,466 Black/admixed ancestry individuals NA Illumina [154263] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179031 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9484) 2,466 Black/admixed ancestry individuals NA Illumina [153214] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178539 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9487) 2,466 Black/admixed ancestry individuals NA Illumina [155552] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178540 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9489) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155526] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178541 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9493) 2,466 Black/admixed ancestry individuals NA Illumina [153570] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178542 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9496) 2,466 Black/admixed ancestry individuals NA Illumina [175837] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178543 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9499) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153574] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178544 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9500) 2,466 Black/admixed ancestry individuals NA Illumina [154613] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178545 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9501) 2,466 Black/admixed ancestry individuals NA Illumina [154131] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178546 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9502) 2,466 Black/admixed ancestry individuals NA Illumina [156233] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178547 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9505) 2,466 Black/admixed ancestry individuals NA Illumina [152715] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178548 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9508) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151420] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178549 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9509) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155915] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178550 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9510) 2,466 Black/admixed ancestry individuals NA Illumina [150465] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178551 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9512) 2,466 Black/admixed ancestry individuals NA Illumina [158080] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178552 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9514) 2,466 Black/admixed ancestry individuals NA Illumina [160426] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178553 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9515) 2,466 Black/admixed ancestry individuals NA Illumina [177007] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178554 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9516) 2,466 Black/admixed ancestry individuals NA Illumina [159488] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178555 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9517) 2,466 Black/admixed ancestry individuals NA Illumina [156026] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178556 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9518) 2,466 Black/admixed ancestry individuals NA Illumina [163310] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178557 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9519) 2,466 Black/admixed ancestry individuals NA Illumina [163919] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178558 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9520) 2,466 Black/admixed ancestry individuals NA Illumina [163289] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178559 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9521) 2,466 Black/admixed ancestry individuals NA Illumina [163874] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178560 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9522) 2,466 Black/admixed ancestry individuals NA Illumina [162183] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178561 Genome-wide sequencing 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in medium VLDL 21,240 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132656 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in small VLDL 21,551 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132657 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in very large VLDL 21,237 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132658 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in very small VLDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132659 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in large VLDL 18,960 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132660 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in medium VLDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132661 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in small VLDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132662 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in very large VLDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132663 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in very small VLDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132664 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in large VLDL 21,239 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132665 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in medium VLDL 21,241 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132666 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in small VLDL 21,558 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 2 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132667 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in very large VLDL 21,548 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132668 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in very small VLDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132669 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Cholesterol ester levels in large HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132670 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in chylomicrons and extremely large VLDL 21,540 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 chylomicron measurement, triglyceride measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132630 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Cholesterol ester levels in large LDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132671 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Cholesterol ester levels in large VLDL 18,960 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90132672 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Cholesterol ester levels in medium HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132673 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Cholesterol ester levels in medium LDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 esterified cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132674 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Cholesterol ester levels in very large HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 esterified cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132675 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in IDL 21,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 free cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90132676 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in large HDL 21,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132677 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in large LDL 21,555 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 6 free cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004611 GCST003665 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in medium HDL 21,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132679 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in chylomicrons and extremely large VLDL 21,542 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 chylomicron measurement, very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132631 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in chylomicrons and extremely large VLDL 18,960 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 chylomicron measurement, very low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132632 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in IDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 lipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90132633 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in IDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 triglyceride measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90132634 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in small HDL 21,558 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132635 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Triglyceride levels in very large HDL 21,536 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132636 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in large LDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132637 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in medium LDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132638 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in small LDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein cholesterol measurement, lipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132639 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in large HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132640 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in medium HDL 21,558 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132641 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in very large HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 phospholipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132642 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in large HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132643 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in medium HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132644 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in small HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132645 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total lipid levels in very large HDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 lipid measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004529, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132646 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in IDL 21,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 phospholipid measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004639, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90132647 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in large LDL 21,550 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132648 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in medium LDL 21,558 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0004611, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132649 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Cholesterol ester levels in medium VLDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0008589 GCST90132650 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of chylomicrons and extremely large VLDL particles 18,960 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 chylomicron measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008596, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132651 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in large VLDL 21,238 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132652 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in medium VLDL 21,240 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132653 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in small VLDL 21,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 free cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132654 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phospholipid levels in large VLDL 21,239 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement, phospholipid measurement http://www.ebi.ac.uk/efo/EFO_0008317, http://www.ebi.ac.uk/efo/EFO_0004639 GCST90132655 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16167) 2,466 Black/admixed ancestry individuals NA Illumina [162451] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177356 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16167) 2,466 Black/admixed ancestry individuals NA Illumina [149749] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179020 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16168) 2,466 Black/admixed ancestry individuals NA Illumina [156741] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177357 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16168) 2,466 Black/admixed ancestry individuals NA Illumina [142296] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179021 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16184) 2,466 Black/admixed ancestry individuals NA Illumina [157394] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177358 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16188) 2,466 Black/admixed ancestry individuals NA Illumina [141568] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177359 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16188) 2,466 Black/admixed ancestry individuals NA Illumina [151058] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179022 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16191) 2,466 Black/admixed ancestry individuals NA Illumina [147184] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177360 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16191) 2,466 Black/admixed ancestry individuals NA Illumina [151660] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179023 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI16192) 2,466 Black/admixed ancestry individuals NA Illumina [158280] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177361 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1622) 2,466 Black/admixed ancestry individuals NA Illumina [151263] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177362 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1623) 2,466 Black/admixed ancestry individuals NA Illumina [154299] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177363 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1625) 2,466 Black/admixed ancestry individuals NA Illumina [162409] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177364 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1626) 2,466 Black/admixed ancestry individuals NA Illumina [152587] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177365 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1627) 2,466 Black/admixed ancestry individuals NA Illumina [154141] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179024 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1628) 2,466 Black/admixed ancestry individuals NA Illumina [158651] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177366 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1629) 2,466 Black/admixed ancestry individuals NA Illumina [200830] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179025 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1631) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [149154] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177367 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1634) 2,466 Black/admixed ancestry individuals NA Illumina [153766] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177368 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1635) 2,466 Black/admixed ancestry individuals NA Illumina [374103] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179026 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1636) 2,466 Black/admixed ancestry individuals NA Illumina [170449] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177369 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1637) 2,466 Black/admixed ancestry individuals NA Illumina [147057] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177370 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1638) 2,466 Black/admixed ancestry individuals NA Illumina [152747] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177371 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1638) 2,466 Black/admixed ancestry individuals NA Illumina [150951] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178822 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1641) 2,466 Black/admixed ancestry individuals NA Illumina [150087] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177372 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI165) 2,466 Black/admixed ancestry individuals NA Illumina [149182] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177373 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1659) 2,466 Black/admixed ancestry individuals NA Illumina [168097] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177374 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI166) 2,466 Black/admixed ancestry individuals NA Illumina [156578] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177375 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI166) 2,466 Black/admixed ancestry individuals NA Illumina [156738] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178823 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1660) 2,466 Black/admixed ancestry individuals NA Illumina [139477] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177376 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1660) 2,466 Black/admixed ancestry individuals NA Illumina [148223] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178824 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1667) 2,466 Black/admixed ancestry individuals NA Illumina [141647] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177377 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1668) 2,466 Black/admixed ancestry individuals NA Illumina [161602] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179027 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1669) 2,466 Black/admixed ancestry individuals NA Illumina [288464] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179028 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI167) 2,466 Black/admixed ancestry individuals NA Illumina [153156] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177378 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI167) 2,466 Black/admixed ancestry individuals NA Illumina [159342] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178825 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1670) 2,466 Black/admixed ancestry individuals NA Illumina [154744] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177379 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1671) 2,466 Black/admixed ancestry individuals NA Illumina [156272] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177380 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1674) 2,466 Black/admixed ancestry individuals NA Illumina [155689] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177381 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1674) 2,466 Black/admixed ancestry individuals NA Illumina [162361] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179029 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1691) 2,466 Black/admixed ancestry individuals NA Illumina [156280] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177382 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1695) 2,466 Black/admixed ancestry individuals NA Illumina [153459] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177383 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1696) 2,466 Black/admixed ancestry individuals NA Illumina [158204] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177384 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1696) 2,466 Black/admixed ancestry individuals NA Illumina [156010] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178826 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1697) 2,466 Black/admixed ancestry individuals NA Illumina [153143] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177385 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1699) 2,466 Black/admixed ancestry individuals NA Illumina [161709] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177386 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI170) 2,466 Black/admixed ancestry individuals NA Illumina [148658] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177387 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1709) 2,466 Black/admixed ancestry individuals NA Illumina [323687] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179030 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1710) 2,466 Black/admixed ancestry individuals NA Illumina [137497] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177388 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1710) 2,466 Black/admixed ancestry individuals NA Illumina [142674] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178827 Genome-wide sequencing 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels in very large HDL 21,542 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 free cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132680 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in HDL 21,555 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132681 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in IDL 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement, intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008595 GCST90132682 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in large HDL 21,558 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132683 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in large LDL 21,552 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132684 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in large VLDL 21,235 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132685 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in LDL 21,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132686 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in medium HDL 21,558 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132687 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in medium LDL 21,559 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132688 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in medium VLDL 21,551 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132689 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in small LDL 21,556 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 total cholesterol measurement, low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132690 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in small VLDL 21,557 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement, very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132691 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total cholesterol levels in very large HDL 21,540 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 total cholesterol measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132692 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Linoleic acid levels 13,527 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 linoleic acid measurement http://www.ebi.ac.uk/efo/EFO_0006807 GCST90132693 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Docosahexaenoic acid levels 13,499 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 docosahexaenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0007761 GCST90132694 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. 3-Hydroxybutyrate levels 24,154 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90132695 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Acetate levels 24,748 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 acetate measurement http://www.ebi.ac.uk/efo/EFO_0010112 GCST90132696 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Acetoacetate levels 19,262 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90132697 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Alanine levels 24,796 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 2 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST003666 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Albumin levels 18,960 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90132699 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Apolipoprotein A1 levels 20,687 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90132700 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Apolipoprotein B levels 20,690 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 apolipoprotein B measurement http://www.ebi.ac.uk/efo/EFO_0004615 GCST90132701 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Average diameter for HDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 high density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008592 GCST90132702 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. CH2 groups in fatty acids 19,021 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90132703 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. CH2 groups to double bonds ratio 13,532 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132704 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI970) 2,466 Black/admixed ancestry individuals NA Illumina [146844] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178610 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9702) 2,466 Black/admixed ancestry individuals NA Illumina [151202] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178611 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9703) 2,466 Black/admixed ancestry individuals NA Illumina [149591] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178612 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9705) 2,466 Black/admixed ancestry individuals NA Illumina [158701] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178613 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9706) 2,466 Black/admixed ancestry individuals NA Illumina [162499] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178614 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9708) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150977] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178615 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9710) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156123] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178616 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI972) 2,466 Black/admixed ancestry individuals NA Illumina [152849] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178617 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9722) 2,466 Black/admixed ancestry individuals NA Illumina [150893] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178618 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9726) 2,466 Black/admixed ancestry individuals NA Illumina [149538] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178619 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI973) 2,466 Black/admixed ancestry individuals NA Illumina [154135] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178620 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9733) 2,466 Black/admixed ancestry individuals NA Illumina [150696] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178621 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9734) 2,466 Black/admixed ancestry individuals NA Illumina [157646] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178622 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9738) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152999] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178623 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9748) 2,466 Black/admixed ancestry individuals NA Illumina [158941] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178624 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9751) 2,466 Black/admixed ancestry individuals NA Illumina [154228] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178625 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9752) 2,466 Black/admixed ancestry individuals NA Illumina [166297] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178626 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI9753) 2,466 Black/admixed ancestry individuals NA Illumina [163593] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178627 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15577) 2,466 Black/admixed ancestry individuals NA Illumina [152718] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177164 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15578) 2,466 Black/admixed ancestry individuals NA Illumina [155432] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177165 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15579) 2,466 Black/admixed ancestry individuals NA Illumina [155195] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177166 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15580) 2,466 Black/admixed ancestry individuals NA Illumina [152833] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177167 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15581) 2,466 Black/admixed ancestry individuals NA Illumina [153344] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177168 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15582) 2,466 Black/admixed ancestry individuals NA Illumina [159519] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177169 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15587) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159662] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177170 Genome-wide sequencing 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Citrate levels 24,770 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90132705 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of IDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 intermediate density lipoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008595 GCST90132706 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of large HDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132707 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of large LDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132708 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of large VLDL particles 18,960 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132709 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of medium HDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132710 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of medium LDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132711 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of medium VLDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132712 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of small HDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132713 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of small LDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90132714 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of small VLDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132715 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of very large HDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90132716 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of very large VLDL particles 18,960 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132717 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Concentration of very small VLDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 very low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008317 GCST90132718 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Creatinine levels 24,810 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 4 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90132719 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Double bonds in fatty acids 15,728 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90132720 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Esterified cholesterol levels 13,497 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 esterified cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008589 GCST90132721 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Fatty acid length 13,476 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90132722 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Free cholesterol levels 13,497 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 free cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0008591 GCST90132723 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Glucose levels 24,679 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90132724 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Glutamine levels 24,462 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 2 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90132725 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Glycerol levels 20,235 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90132726 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Glycine levels 18,734 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 5 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90132727 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Glycoprotein acetyls (mainly a1-acid glycoprotein) 19,270 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 2 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0004555 GCST90132728 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Histidine levels 19,244 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 4 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90132729 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Isoleucine levels 24,776 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90132730 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Lactate levels 24,871 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90132731 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Leucine levels 24,728 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90132732 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Mean diameter of LDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008593 GCST90132733 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Mean diameter of VLDL particles 19,273 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 very low density lipoprotein particle size measurement http://www.ebi.ac.uk/efo/EFO_0008594 GCST90132734 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Monounsaturated fatty acid levels 13,535 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90132735 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Omega-3 fatty acid levels 13,544 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 omega-3 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0010119 GCST90132736 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Omega-6 fatty acid levels 13,506 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 omega-6 polyunsaturated fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005680 GCST90132737 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Omega-7 and omega-9 and saturated fatty acid levels 13,506 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90132738 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Other polyunsaturated fatty acid levels than 18:2 13,549 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90132739 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phenylalanine levels 22,663 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 2 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90132740 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phosphatidylcholine and other choline levels 13,542 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90132741 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Phosphoglycerides levels 13,519 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 glycerophospholipid measurement http://www.ebi.ac.uk/efo/EFO_0007630 GCST90132742 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Pyruvate levels 24,756 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90132743 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Ratio of bis-allylic bonds to double bonds in lipids 13,524 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132744 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Ratio of bis-allylic bonds to total fatty acids in lipids 13,171 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90132745 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Serum total cholesterol levels 21,491 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90132746 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Sphingomyelin levels 13,476 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90132747 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total fatty acid levels 13,505 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0005110 GCST90132748 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Total triglycerides levels 21,545 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST003664 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Tyrosine levels 24,925 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90132750 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Urea levels 18,814 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90132751 Genome-wide genotyping array 2022-09-06 27005778 Kettunen J 2016-03-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/27005778 Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA. Valine levels 24,900 European ancestry individuals NA Affymetrix, Illumina, Perlegen [12133295] (imputed) 3 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90132752 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15630) 2,466 Black/admixed ancestry individuals NA Illumina [152456] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177195 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15631) 2,466 Black/admixed ancestry individuals NA Illumina [152876] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177196 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15632) 2,466 Black/admixed ancestry individuals NA Illumina [154012] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177197 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15633) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160091] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177198 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15634) 2,466 Black/admixed ancestry individuals NA Illumina [152960] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177199 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15635) 2,466 Black/admixed ancestry individuals NA Illumina [155614] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177200 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15636) 2,466 Black/admixed ancestry individuals NA Illumina [156320] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177201 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15646) 2,466 Black/admixed ancestry individuals NA Illumina [156214] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177202 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15647) 2,466 Black/admixed ancestry individuals NA Illumina [195873] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179013 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15648) 2,466 Black/admixed ancestry individuals NA Illumina [162865] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177203 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15649) 2,466 Black/admixed ancestry individuals NA Illumina [155830] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177204 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1565) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151262] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177205 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1566) 2,466 Black/admixed ancestry individuals NA Illumina [152098] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177206 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15660) 2,466 Black/admixed ancestry individuals NA Illumina [150709] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177207 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15661) 2,466 Black/admixed ancestry individuals NA Illumina [150137] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177208 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15667) 2,466 Black/admixed ancestry individuals NA Illumina [166259] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177209 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15668) 2,466 Black/admixed ancestry individuals NA Illumina [149746] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177210 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15669) 2,466 Black/admixed ancestry individuals NA Illumina [169797] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177211 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15670) 2,466 Black/admixed ancestry individuals NA Illumina [152067] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177212 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1568) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152871] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177213 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15682) 2,466 Black/admixed ancestry individuals NA Illumina [157145] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177214 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15683) 2,466 Black/admixed ancestry individuals NA Illumina [150460] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177215 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15685) 2,466 Black/admixed ancestry individuals NA Illumina [166584] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177216 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1569) 2,466 Black/admixed ancestry individuals NA Illumina [166396] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177217 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15690) 2,466 Black/admixed ancestry individuals NA Illumina [147718] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177218 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15588) 2,466 Black/admixed ancestry individuals NA Illumina [154244] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177171 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15592) 2,466 Black/admixed ancestry individuals NA Illumina [162855] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177172 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15595) 2,466 Black/admixed ancestry individuals NA Illumina [152499] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177173 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15598) 2,466 Black/admixed ancestry individuals NA Illumina [156044] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177174 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15599) 2,466 Black/admixed ancestry individuals NA Illumina [153713] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177175 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1560) 2,466 Black/admixed ancestry individuals NA Illumina [154713] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177176 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1560) 2,466 Black/admixed ancestry individuals NA Illumina [156170] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178806 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15600) 2,466 Black/admixed ancestry individuals NA Illumina [151879] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177177 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15601) 2,466 Black/admixed ancestry individuals NA Illumina [157490] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177178 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15602) 2,466 Black/admixed ancestry individuals NA Illumina [154335] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177179 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15603) 2,466 Black/admixed ancestry individuals NA Illumina [152392] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177180 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15604) 2,466 Black/admixed ancestry individuals NA Illumina [153692] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177181 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15605) 2,466 Black/admixed ancestry individuals NA Illumina [156603] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177182 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15606) 2,466 Black/admixed ancestry individuals NA Illumina [152069] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177183 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15607) 2,466 Black/admixed ancestry individuals NA Illumina [155660] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177184 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15608) 2,466 Black/admixed ancestry individuals NA Illumina [157327] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177185 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15609) 2,466 Black/admixed ancestry individuals NA Illumina [154860] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177186 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15614) 2,466 Black/admixed ancestry individuals NA Illumina [150518] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177187 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15619) 2,466 Black/admixed ancestry individuals NA Illumina [155418] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177188 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15622) 2,466 Black/admixed ancestry individuals NA Illumina [149094] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177189 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15625) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157348] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177190 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15626) 2,466 Black/admixed ancestry individuals NA Illumina [157140] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177191 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15627) 2,466 Black/admixed ancestry individuals NA Illumina [158608] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177192 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15628) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [159381] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177193 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15629) 2,466 Black/admixed ancestry individuals NA Illumina [156094] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177194 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15697) 2,466 Black/admixed ancestry individuals NA Illumina [158680] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177219 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1570) 2,466 Black/admixed ancestry individuals NA Illumina [159570] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177220 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15700) 2,466 Black/admixed ancestry individuals NA Illumina [151093] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177221 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15703) 2,466 Black/admixed ancestry individuals NA Illumina [153436] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177222 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15705) 2,466 Black/admixed ancestry individuals NA Illumina [149903] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177223 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15708) 2,466 Black/admixed ancestry individuals NA Illumina [162716] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177224 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15715) 2,466 Black/admixed ancestry individuals NA Illumina [152563] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177225 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1572) 2,466 Black/admixed ancestry individuals NA Illumina [162030] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177226 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1572) 2,466 Black/admixed ancestry individuals NA Illumina [149822] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178807 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15723) 2,466 Black/admixed ancestry individuals NA Illumina [166945] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177227 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15726) 2,466 Black/admixed ancestry individuals NA Illumina [158146] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177228 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15727) 2,466 Black/admixed ancestry individuals NA Illumina [141992] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177229 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15735) 2,466 Black/admixed ancestry individuals NA Illumina [139608] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177230 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15736) 2,466 Black/admixed ancestry individuals NA Illumina [156878] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177231 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15737) 2,466 Black/admixed ancestry individuals NA Illumina [155338] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177232 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15738) 2,466 Black/admixed ancestry individuals NA Illumina [145130] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177233 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15739) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [154293] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177234 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1574) 2,466 Black/admixed ancestry individuals NA Illumina [142937] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177235 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15740) 2,466 Black/admixed ancestry individuals NA Illumina [150696] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177236 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15746) 2,466 Black/admixed ancestry individuals NA Illumina [158778] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177237 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15747) 2,466 Black/admixed ancestry individuals NA Illumina [156557] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177238 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15750) 2,466 Black/admixed ancestry individuals NA Illumina [155243] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177239 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1576) 2,466 Black/admixed ancestry individuals NA Illumina [162696] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177240 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15761) 2,466 Black/admixed ancestry individuals NA Illumina [154743] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177241 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI15762) 2,466 Black/admixed ancestry individuals NA Illumina [158524] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177242 Genome-wide sequencing 2022-01-26 32663566 Tashjian RZ 2020-07-11 J Shoulder Elbow Surg www.ncbi.nlm.nih.gov/pubmed/32663566 Genetic Variants Associated With Rotator Cuff Tearing Utilizing Multiple Population-Based Genetic Resources. Rotator cuff injury 5,701 European ancestry cases, 406,310 European ancestry controls NA Affymetrix [17136336] (imputed) 3 rotator cuff tear http://www.ebi.ac.uk/efo/EFO_1001250 GCST90044700 Genome-wide genotyping array 2022-01-31 33967749 Ooi BNS 2021-04-22 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/33967749 Robust Performance of Potentially Functional SNPs in Machine Learning Models for the Prediction of Atorvastatin-Induced Myalgia. Atorvastatin-induced myalgia 14 Chinese ancestry cases, 74 Chinese ancestry controls, 12 Indian ancestry cases, 45 Indian ancestry controls, 4 Malay ancestry cases, 34 Malay ancestry controls NA Illumina [4554532] 5 response to atorvastatin, Myalgia http://www.ebi.ac.uk/efo/EFO_0010124, http://purl.obolibrary.org/obo/HP_0003326 GCST90093311 Genome-wide sequencing 2021-11-09 34634379 Mei L 2021-10-08 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34634379 Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders. Major depressive disorder 16,823 European ancestry cases, 25,632 European ancestry controls NA NR [NR] 25 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90085695 Genome-wide genotyping array 2021-11-09 34634379 Mei L 2021-10-08 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34634379 Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders. Anxiety and stress-related disorders 12,665 European ancestry cases, 19,225 European ancestry controls NA NR [NR] 2 anxiety, stress-related disorder http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0010098 GCST90085696 Genome-wide genotyping array 2021-11-09 34634379 Mei L 2021-10-08 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/34634379 Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders. Major depressive disorder or stress-related disorder 16,823 European ancestry cases, 25,632 European ancestry controls, 12,665 European ancestry cases, 19,225 European ancestry controls NA NR [NR] 242 anxiety, stress-related disorder, major depressive disorder http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0010098, http://purl.obolibrary.org/obo/MONDO_0002009 GCST90085697 Genome-wide genotyping array 2022-01-06 34659352 Bensenor I 2021-09-29 Front Genet www.ncbi.nlm.nih.gov/pubmed/34659352 Genome-Wide Association of Proprotein Convertase Subtilisin/Kexin Type 9 Plasma Levels in the ELSA-Brasil Study. Plasma PCSK9 levels 96 Black ancestry individuals, 178 individuals, 480 White ancestry individuals, 39 Asian ancestry individuals, 17 indigenous ancestry individuals NA Affymetrix [11524071] (imputed) 55 PCSK9 protein measurement http://www.ebi.ac.uk/efo/EFO_0006899 GCST90085917 Genome-wide genotyping array 2022-02-04 33829662 Cutrer FM 2021-04-07 Mol Genet Genomic Med www.ncbi.nlm.nih.gov/pubmed/33829662 Genetic variants related to successful migraine prophylaxis with verapamil. Response to verapamil in migraine 21 cases, 14 controls 185 individuals Illumina [NR] 0 response to verapamil http://www.ebi.ac.uk/efo/EFO_0020862 GCST90093309 Exome-wide sequencing 2022-02-02 34158603 Liu X 2021-06-22 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/34158603 New genetic variants associated with major adverse cardiovascular events in patients with acute coronary syndromes and treated with clopidogrel and aspirin. Major adverse cardiovascular events in response to aspirin and clopidogrel treatment 51 Han Chinese ancestry cases, 117 Han Chinese ancestry controls 123 Han Chinese ancestry cases, 1,580 Han Chinese ancestry controls NR [127834] 8 response to clopidogrel, response to acetylsalicylate, major adverse cardiovascular event measurement http://purl.obolibrary.org/obo/GO_1903493, http://purl.obolibrary.org/obo/GO_1903492, http://www.ebi.ac.uk/efo/EFO_0020863 GCST90093363 Exome-wide sequencing 2021-11-25 31732565 van 't Hof FNG 2019-11-15 Neurology www.ncbi.nlm.nih.gov/pubmed/31732565 Exome-chip association analysis of intracranial aneurysms. Intracranial aneurysm 995 European ancestry cases, 2,080 European ancestry controls 425 European ancestry cases, 311 European ancestry controls Illumina [218523] 0 brain aneurysm http://www.ebi.ac.uk/efo/EFO_0003870 GCST012536 Exome genotyping array [Exome array] 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:6)_[M+OAc]1-/Phosphatidylserine(40:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060874 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(36:7)_[M+OAc]1-/Phosphatidylserine(40:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060869 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:3)_[M+OAc]1-/Phosphatidylserine(41:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060902 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:4)_[M+H]1+/Phosphatidylethanolamine(40:3)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 57 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060805 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:4)_[M+H]1+/Phosphatidylethanolamine(40:4)_[M+H]1+/Phosphatidate(42:5)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 77 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060799 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:4)_[M+OAc]1-/Phosphatidylserine(41:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060901 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:5)_[M+H]1+/Phosphatidylethanolamine(40:5)_[M+H]1+/Phosphatidate(42:6)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060794 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:5)_[M+OAc]1-/Phosphatidylserine(41:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060899 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:6)_[M+H]1+/Phosphatidylethanolamine(40:6)_[M+H]1+/Phosphatidate(42:7)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 34 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060790 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(37:6)_[M+OAc]1-/Phosphatidylserine(41:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060896 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:2)_[M+H]1+/Phosphatidylethanolamine(41:2)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 45 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060838 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:2)_[M+OAc]1-/Phosphatidylserine(42:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060931 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:3)_[M+H]1+/Phosphatidylethanolamine(41:3)_[M+H]1+/Phosphatidate(43:4)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 97 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060833 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:3)_[M+OAc]1-/Phosphatidylserine(42:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 92 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060926 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:4)_[M+H]1+/Phosphatidylethanolamine(41:4)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 87 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060829 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:4)_[M+OAc]1-/Phosphatidylserine(42:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 78 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060922 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:5)_[M+H]1+/Phosphatidylethanolamine(41:5)_[M+H]1+/Phosphatidate(43:6)_[M+NH4]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 71 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060822 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:5)_[M+OAc]1-/Phosphatidylserine(42:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060921 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:6)_[M+H]1+/Phosphatidylethanolamine(41:6)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 34 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060818 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:6)_[M+OAc]1-/Phosphatidylserine(42:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060918 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:7)_[M+OAc]1-/Phosphatidylserine(42:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060914 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(38:8)_[M+OAc]1-/Phosphatidylserine(42:7)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060910 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(39:6)_[M+OAc]1-/Phosphatidylserine(43:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 16 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060939 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060883 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:4)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060967 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:4)_[M+OAc]1-/Phosphatidylserine(44:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 61 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060962 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:5)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 69 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060875 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:5)_[M+OAc]1-/Phosphatidylserine(44:4)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 68 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060959 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:6)_[M+H]1+/Phosphatidylethanolamine(43:6)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 55 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060870 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:6)_[M+OAc]1-/Phosphatidylserine(44:5)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 37 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060957 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylcholine(40:7)_[M+OAc]1-/Phosphatidylserine(44:6)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060953 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_42:1_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90060215 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_42:1_[M+OAc]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylcholine ether measurement http://www.ebi.ac.uk/efo/EFO_0010227 GCST90060246 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_42:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 11 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060212 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_42:2_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 4 phosphatidylethanolamine ether measurement http://www.ebi.ac.uk/efo/EFO_0010229 GCST90060204 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide_42:2_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylinositol measurement http://www.ebi.ac.uk/efo/EFO_0010230 GCST90060213 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(34:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 sterol measurement http://www.ebi.ac.uk/efo/EFO_0010231 GCST90060601 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(40:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 46 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90060619 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(40:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 33 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060618 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(40:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060642 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(40:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 27 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060617 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(41:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 16 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060624 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(41:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 17 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060622 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(41:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 49 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060620 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(42:0)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 17 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060630 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(42:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060629 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(42:1)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060661 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(42:10)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060648 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(42:11)_[M+OAc]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060645 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Ceramide(42:2)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 genotoxic compound exposure measurement http://www.ebi.ac.uk/efo/EFO_0010233 GCST90060628 Genome-wide genotyping array 2021-11-09 30675382 Leblond CS 2019-01-21 NPJ Genom Med www.ncbi.nlm.nih.gov/pubmed/30675382 Both rare and common genetic variants contribute to autism in the Faroe Islands. Autism 36 European ancestry, 176 European ancestry controls NA Illumina [1690491] (imputed) 13 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST012498 Genome-wide genotyping array 2021-12-03 34599228 Chenoweth MJ 2021-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34599228 Analyses of nicotine metabolism biomarker genetics stratified by sex in African and European Americans. Nicotine metabolite ratio in current smokers 503 African American or Afro-Caribbean individuals 442 African American or Afro-Caribbean individuals Illumina [17199451] (imputed) 0 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST90061016 Genome-wide genotyping array 2021-12-03 34599228 Chenoweth MJ 2021-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34599228 Analyses of nicotine metabolism biomarker genetics stratified by sex in African and European Americans. Nicotine metabolite ratio in current smokers 352 African American or Afro-Caribbean individuals 254 African American or Afro-Caribbean individuals Illumina [17379949] (imputed) 0 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST90061017 Genome-wide genotyping array 2021-12-03 34599228 Chenoweth MJ 2021-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34599228 Analyses of nicotine metabolism biomarker genetics stratified by sex in African and European Americans. Nicotine metabolite ratio in current smokers 389 European ancestry individuals NA Illumina [7602147] (imputed) 1 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST90061018 Genome-wide genotyping array 2021-12-03 34599228 Chenoweth MJ 2021-10-01 Sci Rep www.ncbi.nlm.nih.gov/pubmed/34599228 Analyses of nicotine metabolism biomarker genetics stratified by sex in African and European Americans. Nicotine metabolite ratio in current smokers 541 European ancestry individuals NA Illumina [7599895] (imputed) 1 nicotine metabolite ratio http://www.ebi.ac.uk/efo/EFO_0007794 GCST90061019 Genome-wide genotyping array 2021-10-19 33992511 Chang X 2021-04-07 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/33992511 The association of genetically determined serum glycine with cardiovascular risk in East Asians. Glycine levels 1,324 Chinese ancestry individuals NA NR [NR] (imputed) 2 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90044914 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_37:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 20 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060299 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_37:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 19 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060296 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_38:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 19 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060320 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_38:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 39 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060317 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_38:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 44 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060315 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_38:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 46 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060313 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_38:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 31 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060310 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_39:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060350 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_39:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 28 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060346 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_40:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060365 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine_42:9_[M+H]1+/Phosphatidate_44:10_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060404 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_34:1_[M-H]1-/Phosphatidylethanolamine-P_34:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 3 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060238 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_34:2_[M-H]1-/Phosphatidylethanolamine-P_34:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060234 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_34:3_[M-H]1-/Phosphatidylethanolamine-P_34:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 25 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060232 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_36:1_[M-H]1-/Phosphatidylethanolamine-P_36:0_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060265 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_36:2_[M-H]1-/Phosphatidylethanolamine-P_36:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060262 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_36:3_[M-H]1-/Phosphatidylethanolamine-P_36:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 16 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060259 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_36:4_[M-H]1-/Phosphatidylethanolamine-P_36:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 17 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060258 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_36:5_[M-H]1-/Phosphatidylethanolamine-P_36:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 24 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060256 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_36:5_[M+H]1+/Phosphatidylethanolamine-P_36:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060257 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_38:2_[M-H]1-/Phosphatidylethanolamine-P_38:1_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060300 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_38:3_[M-H]1-/Phosphatidylethanolamine-P_38:2_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 22 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060297 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_38:4_[M-H]1-/Phosphatidylethanolamine-P_38:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060294 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_38:5_[M-H]1-/Phosphatidylethanolamine-P_38:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 27 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060292 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_38:5_[M+H]1+/Phosphatidylethanolamine-P_38:4_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060293 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_38:6_[M-H]1-/Phosphatidylethanolamine-P_38:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 17 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060288 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_38:6_[M+H]1+/Phosphatidylethanolamine-P_38:5_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060291 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_40:4_[M-H]1-/Phosphatidylethanolamine-P_40:3_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060347 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_40:5_[M-H]1-/Phosphatidylethanolamine-P_40:4_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 27 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060343 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_40:6_[M-H]1-/Phosphatidylethanolamine-P_40:5_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 15 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060337 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O_40:6_[M+H]1+/Phosphatidylethanolamine-P_40:5_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060342 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O(34:1)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060656 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O(38:4)_[M-H]1-/Phosphatidylcholine-O(35:4)_[M-H]1-/Phosphatidylcholine-P(35:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 68 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060711 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-O(38:6)_[M+H]1+/Phosphatidylcholine-P(35:5)_[M+H]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 58 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060709 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-P_38:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060282 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-P_38:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060287 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-P_40:6_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060329 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-P_40:6_[M+H]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060336 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine-P_40:7_[M-H]1- levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060324 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Phosphatidylethanolamine(30:3)_[M-H]1- levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90060632 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_30:0_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 30:0 measurement http://www.ebi.ac.uk/efo/EFO_0020052 GCST90060161 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_30:1_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 30:1 measurement http://www.ebi.ac.uk/efo/EFO_0020051 GCST90060159 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_32:0_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0020054 GCST90060169 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_32:0_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0020054 GCST90060185 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_32:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90060184 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_32:2_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 diacylglycerol 32.2 measurement http://www.ebi.ac.uk/efo/EFO_0020055 GCST90060168 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_33:1_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 6 diacylglycerol 33:1 measurement http://www.ebi.ac.uk/efo/EFO_0020056 GCST90060173 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_33:3_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 33:3 measurement http://www.ebi.ac.uk/efo/EFO_0020057 GCST90060172 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_34:0_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 2 diacylglycerol 34:0 measurement http://www.ebi.ac.uk/efo/EFO_0020058 GCST90060181 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_34:1_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 22 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90060179 Genome-wide genotyping array 2022-02-22 34729928 El Rouby N 2021-11-02 Clin Transl Sci www.ncbi.nlm.nih.gov/pubmed/34729928 Genomewide association analysis of warfarin dose requirements in Middle Eastern and North African populations. Warfarin dose variability 132 Arab ancestry individuals 50 Egyptian ancestry individuals Illumina [1132000] 1 dose response design, response to warfarin http://www.ebi.ac.uk/efo/EFO_0001757, http://www.ebi.ac.uk/efo/EFO_0009167 GCST90094874 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_34:1_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90060196 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_34:2_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 33 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90060178 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_34:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90060195 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_34:3_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 7 diacylglycerol 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0020059 GCST90060177 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_34:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0020059 GCST90060194 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:1_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 2 diacylglycerol 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010354 GCST90060193 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:2_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 43 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90060191 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90060209 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:3_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 42 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90060189 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:3_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90060208 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:4_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 8 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90060188 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:4_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90060206 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_36:5_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 1 diacylglycerol 36:5 measurement http://www.ebi.ac.uk/efo/EFO_0020064 GCST90060187 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_38:3_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 45 diacylglycerol 38:3 measurement http://www.ebi.ac.uk/efo/EFO_0020065 GCST90060203 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_38:4_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 40 diacylglycerol 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0020066 GCST90060201 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_38:5_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 46 diacylglycerol 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0020067 GCST90060200 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_38:6_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 33 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90060199 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_39:2_[M+NH4]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90060227 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_42:7_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 36 diacylglycerol 42:7 measurement http://www.ebi.ac.uk/efo/EFO_0020068 GCST90060226 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_44:6_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 9 diacylglycerol 44:6 measurement http://www.ebi.ac.uk/efo/EFO_0020070 GCST90060245 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol_44:7_[M+H-H2O]1+ levels 13,814 British ancestry individuals NA Affymetrix [87696910] (imputed) 38 diacylglycerol 44:7 measurement http://www.ebi.ac.uk/efo/EFO_0020069 GCST90060240 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(30:0)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 diacylglycerol 30:0 measurement http://www.ebi.ac.uk/efo/EFO_0020052 GCST90060599 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(30:1)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 diacylglycerol 30:1 measurement http://www.ebi.ac.uk/efo/EFO_0020051 GCST90060597 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(32:0)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 0 diacylglycerol 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0020054 GCST90060604 Genome-wide genotyping array 2022-02-17 34503513 Harshfield EL 2021-09-10 BMC Med www.ncbi.nlm.nih.gov/pubmed/34503513 Genome-wide analysis of blood lipid metabolites in over 5000 South Asians reveals biological insights at cardiometabolic disease loci. Diacylglycerol(32:2)_[M+H-H2O]1+ levels 5,662 Pakistani ancestry individuals NA Illumina [6720657] (imputed) 17 diacylglycerol 32.2 measurement http://www.ebi.ac.uk/efo/EFO_0020055 GCST90060603 Genome-wide genotyping array 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Serine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90134364 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Spermidine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90134365 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. lysoPhosphatidylcholine acyl C16:0 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90134366 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. lysoPhosphatidylcholine acyl C16:1 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90134367 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. lysoPhosphatidylcholine acyl C20:3 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90134368 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Phosphatidylcholine diacyl C34:4 levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 phosphatidylcholine 34:4 measurement http://www.ebi.ac.uk/efo/EFO_0010378 GCST90134369 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Hexose levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 hexose measurement http://www.ebi.ac.uk/efo/EFO_0007631 GCST90134370 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Aspartate levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90134371 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Decanoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 6 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90134372 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Hexanoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 4 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90134373 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Octanoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 3 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90134374 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Decenoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 5 decenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021803 GCST90134375 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Dodecanoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 7 dodecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021804 GCST90134376 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Symmetric dimethylarginine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 symmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006523 GCST90134377 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Hydroxyvalerylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 hydroxyvalerylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021805 GCST90134378 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Hexadecenoylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 hexadecenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021806 GCST90134379 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Butyrylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 4 butyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020010 GCST90134380 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Carnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90134381 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Acetylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90134382 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Taurine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90134383 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Sarcosine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90134384 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Propionylcarnitine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 2 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90134385 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Serotonin levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90134386 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Lysine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90134387 Genome-wide genotyping array, Exome-wide sequencing 2022-09-06 35888728 Konig E 2022-06-29 Metabolites www.ncbi.nlm.nih.gov/pubmed/35888728 Whole Exome Sequencing Enhanced Imputation Identifies 85 Metabolite Associations in the Alpine CHRIS Cohort. Putrescine levels 5,505 European ancestry individuals NA Illumina [624571] (imputed) 1 putrescine measurement http://www.ebi.ac.uk/efo/EFO_0021810 GCST90134388 Genome-wide genotyping array, Exome-wide sequencing 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta maximum area 32,590 European ancestry individuals NA NR [9753033] 52 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137440 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta minimum area 32,590 European ancestry individuals 2,787 European ancestry individuals NR [9753033] 0 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137441 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta maximum area 32,590 European ancestry individuals NA NR [9753033] 36 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137442 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta minimum area 32,590 European ancestry individuals 2,787 European ancestry individuals NR [9753033] 0 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137443 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta distensibility 29,895 European ancestry individuals NA NR [9753033] 10 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137444 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta distensibility 29,895 European ancestry individuals NA NR [9753033] 7 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137445 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta distensibility (MTAG) 29,895 European ancestry individuals NA NR [9753033] 26 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137446 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta distensibility (MTAG) 29,895 European ancestry individuals NA NR [9753033] 13 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137447 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta minimum area (MTAG) 32,590 European ancestry individuals 2,787 European ancestry individuals NR [9753033] 0 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137448 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta minimum area (MTAG) 32,590 European ancestry individuals 2,787 European ancestry individuals NR [9753033] 0 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137449 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta maximum area (MTAG) 32,590 European ancestry individuals NA NR [9753033] 47 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137450 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta maximum area (MTAG) 32,590 European ancestry individuals NA NR [9753033] 29 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137451 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta minimum area 15,817 European ancestry men NA NR [NR] 29 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137452 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta minimum area 15,817 European ancestry men NA NR [NR] 18 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137453 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Ascending aorta minimum area 16,773 European ancestry women NA NR [NR] 30 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137454 Genome-wide genotyping array 2022-09-21 35922433 Francis CM 2022-08-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35922433 Genome-wide associations of aortic distensibility suggest causality for aortic aneurysms and brain white matter hyperintensities. Descending aorta minimum area 16,773 European ancestry women NA NR [NR] 16 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90137455 Genome-wide genotyping array 2022-06-21 35289444 Kuusisto S 2022-03-15 J Intern Med www.ncbi.nlm.nih.gov/pubmed/35289444 Genetic and observational evidence: No independent role for cholesterol efflux over static HDL concentration measures in CHD risk assessment. High-density lipoprotein mediated cholesterol efflux capacity 20,372 Finnish ancestry individuals NA NR [NR] 2 cholesterol efflux capacity measurement http://www.ebi.ac.uk/efo/EFO_0009132 GCST90104624 Genome-wide genotyping array 2022-06-21 35289444 Kuusisto S 2022-03-15 J Intern Med www.ncbi.nlm.nih.gov/pubmed/35289444 Genetic and observational evidence: No independent role for cholesterol efflux over static HDL concentration measures in CHD risk assessment. High-density lipoprotein mediated cholesterol efflux capacity (adjusted for HDL-C and triglycerides) 20,372 Finnish ancestry individuals NA NR [NR] 0 cholesterol efflux capacity measurement, triglyceride measurement, high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0009132, http://www.ebi.ac.uk/efo/EFO_0004530, http://www.ebi.ac.uk/efo/EFO_0004612 GCST90104625 Genome-wide genotyping array 2022-06-21 35289444 Kuusisto S 2022-03-15 J Intern Med www.ncbi.nlm.nih.gov/pubmed/35289444 Genetic and observational evidence: No independent role for cholesterol efflux over static HDL concentration measures in CHD risk assessment. HDL cholesterol levels 20,372 Finnish ancestry individuals NA NR [NR] 2 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90104626 Genome-wide genotyping array 2022-07-29 28242751 Delgado GE 2017-02-27 J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/28242751 Serum Uromodulin and Mortality Risk in Patients Undergoing Coronary Angiography. Serum uromodulin concentration 2,826 European ancestry individuals NA Affymetrix [NR] (imputed) 1 uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0021778 GCST90131429 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Melon liking 159,441 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094800 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Milk chocolate liking 159,434 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094801 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Pasta liking 159,413 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094808 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Pears liking 159,468 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094809 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Pizza liking 159,347 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094810 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Plain yoghurt liking 158,675 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094811 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Plum liking 159,369 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094812 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Pollock liking 130,936 European ancestry individuals NA Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094813 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Pork chop liking 158,434 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094814 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Porridge liking 159,122 European ancestry individuals NA Affymetrix [11353280] (imputed) 9 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094815 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Potatoes liking 159,579 European ancestry individuals NA Affymetrix [11353280] (imputed) 1 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094816 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Prawns liking 157,990 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094817 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Raw carrot liking 159,303 European ancestry individuals NA Affymetrix [11353280] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094818 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Red meat liking 158,624 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094819 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Marzipan liking 159,348 European ancestry individuals NA Affymetrix [11353280] (imputed) 7 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094797 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Mayonnaise liking 159,361 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094798 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-meat liking (derived food-liking factor) 158,509 European ancestry individuals NA Affymetrix [9578209] (imputed) 8 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094799 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Milky sweets liking 159,393 European ancestry individuals NA Affymetrix [9614293] (imputed) 11 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094802 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Mushroom liking 159,454 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094803 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. F-oily fish liking (derived food-liking factor) 158,547 European ancestry individuals NA Affymetrix [9609308] (imputed) 10 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094804 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Onion liking 159,518 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094805 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Orange juice liking 159,473 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 2 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094806 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Oranges liking 159,458 European ancestry individuals NA Affymetrix [11353280] (imputed) 5 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094807 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Red wine liking 158,425 European ancestry individuals 26,154 European, Central Asian and unknown ancestry individuals Affymetrix [11353280] (imputed) 0 red wine liking measurement http://www.ebi.ac.uk/efo/EFO_0006947 GCST90094820 Genome-wide genotyping array 2022-08-04 35585065 May-Wilson S 2022-05-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35585065 Large-scale GWAS of food liking reveals genetic determinants and genetic correlations with distinct neurophysiological traits. Roast chicken liking 158,556 European ancestry individuals NA Affymetrix [11353280] (imputed) 3 taste liking measurement http://www.ebi.ac.uk/efo/EFO_0010155 GCST90094821 Genome-wide genotyping array 2022-07-29 35470158 Saevarsdottir S 2022-04-25 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/35470158 Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset. Rheumatoid arthritis 26,612 European ancestry cases, 869,454 European ancestry controls, 4,701 cases, 125,923 controls NA Affymetrix, Illumina [64000000] (imputed) 51 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90131437 Genome-wide genotyping array, Genome-wide sequencing 2022-07-29 35470158 Saevarsdottir S 2022-04-25 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/35470158 Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset. Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive) 14,551 European ancestry cases, 846,260 European ancestry controls, 3,468 cases, 145,344 controls NA Affymetrix, Illumina [64000000] (imputed) 57 rheumatoid arthritis, ACPA-positive rheumatoid arthritis, rheumatoid factor seropositivity measurement http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0009459, http://www.ebi.ac.uk/efo/EFO_0007791 GCST90131438 Genome-wide genotyping array, Genome-wide sequencing 2022-07-29 35470158 Saevarsdottir S 2022-04-25 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/35470158 Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset. Rheumatoid arthritis (rheumatoid factor and anti-cyclic citrullinated peptide seronegative) 7,079 European ancestry cases, 872,159 European ancestry controls, 1,436 cases, 143,312 controls NA Affymetrix, Illumina [64000000] (imputed) 6 rheumatoid arthritis, ACPA-negative rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685, http://www.ebi.ac.uk/efo/EFO_0009460 GCST90131439 Genome-wide genotyping array, Genome-wide sequencing 2022-08-03 35470676 Kanbay M 2022-04-26 J Am Heart Assoc www.ncbi.nlm.nih.gov/pubmed/35470676 Weak Association Between Genetic Markers of Hyperuricemia and Cardiorenal Outcomes: Insights From the STANISLAS Study Cohort With a 20-Year Follow-Up. Serum uric acid levels 1,573 individuals from up to 1,006 families NA NR [NR] 5 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90131442 Genome-wide genotyping array 2022-05-24 35216288 Pleic N 2022-02-16 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/35216288 Genome-Wide Association Analysis and Genomic Prediction of Thyroglobulin Plasma Levels. Thyroglobulin levels 2,190 European ancestry individuals NA Illumina [6554718] (imputed) 2 thyroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010050 GCST90103791 Genome-wide genotyping array 2022-08-05 35543701 Murphy WA 2022-05-11 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/35543701 Pharmacogenomic Study of Statin-Associated Muscle Symptoms in the ODYSSEY OUTCOMES Trial. Statin intolerance or statin-associated muscle symptoms 819 European ancestry cases, 8,365 European ancestry controls, 49 Asian ancestry cases, 546 Asian ancestry controls, 14 Black cases, 282 Black controls, 12 cases, 530 controls NA Illumina [8921030] (imputed) 6 response to statin, muscle tissue disorder http://purl.obolibrary.org/obo/GO_0036273, http://purl.obolibrary.org/obo/MONDO_0003939 GCST90131947 Genome-wide genotyping array, Exome-wide sequencing 2022-08-05 35543701 Murphy WA 2022-05-11 Circ Genom Precis Med www.ncbi.nlm.nih.gov/pubmed/35543701 Pharmacogenomic Study of Statin-Associated Muscle Symptoms in the ODYSSEY OUTCOMES Trial. Maximum creatine kinase levels in statin users 8,320 European ancestry individuals, 549 Asian ancestry individuals, 256 Black individuals, 505 individuals NA Illumina [8921030] (imputed) 3 response to statin, creatine kinase measurement http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0004534 GCST90131948 Genome-wide genotyping array, Exome-wide sequencing 2022-06-16 35124268 Li J 2022-02-03 Clin Gastroenterol Hepatol www.ncbi.nlm.nih.gov/pubmed/35124268 Mendelian Randomization Analysis Reveals No Causal Relationship Between Nonalcoholic Fatty Liver Disease and Severe COVID-19. Nonalcoholic fatty liver disease 3,711 European ancestry cases, 426,252 European ancestry controls NA NR [NR] 5 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90104598 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (midendocanthion to pogonion) 272 Korean ancestry individuals NA NR [7375270] (imputed) 6 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162619 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (nasion to pogonion) 272 Korean ancestry individuals NA NR [7375270] (imputed) 8 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162620 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (subnasale to pogonion) 272 Korean ancestry individuals NA NR [7375270] (imputed) 6 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162621 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (intercanthal width) 272 Korean ancestry individuals NA NR [7375270] (imputed) 4 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162601 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (outercanthal width) 272 Korean ancestry individuals NA NR [7375270] (imputed) 4 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162602 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (interpalpebral superius length) 272 Korean ancestry individuals NA NR [7375270] (imputed) 6 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162603 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (interpalpebral inferius length) 272 Korean ancestry individuals NA NR [7375270] (imputed) 5 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162604 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (left palpebral fissure length) 272 Korean ancestry individuals NA NR [7375270] (imputed) 2 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162605 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (right palpebral fissure length) 272 Korean ancestry individuals NA NR [7375270] (imputed) 6 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162606 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (mouth width) 272 Korean ancestry individuals NA NR [7375270] (imputed) 4 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162607 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (nasal width) 272 Korean ancestry individuals NA NR [7375270] (imputed) 1 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162608 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (subnasale to left alare) 272 Korean ancestry individuals NA NR [7375270] (imputed) 6 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162609 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (subnasale to right alare) 272 Korean ancestry individuals NA NR [7375270] (imputed) 10 facial width measurement http://www.ebi.ac.uk/efo/EFO_0007855 GCST90162610 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (left palpebrale fissure height) 272 Korean ancestry individuals NA NR [7375270] (imputed) 6 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162611 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (right palpebrale fissure height) 272 Korean ancestry individuals NA NR [7375270] (imputed) 4 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162612 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (philtrum height) 272 Korean ancestry individuals NA NR [7375270] (imputed) 2 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162613 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (labiale inferius to pogonion) 272 Korean ancestry individuals NA NR [7375270] (imputed) 3 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162614 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (midendocanthion to labiale superius ) 272 Korean ancestry individuals NA NR [7375270] (imputed) 6 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162615 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (midendocanthion to subnasale) 272 Korean ancestry individuals NA NR [7375270] (imputed) 4 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162616 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (nasal bridge height) 272 Korean ancestry individuals NA NR [7375270] (imputed) 8 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162617 Genome-wide genotyping array 2022-10-11 35970861 Cha MY 2022-08-15 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35970861 Classification of early age facial growth pattern and identification of the genetic basis in two Korean populations. Facial phenotypes (nasal height) 272 Korean ancestry individuals NA NR [7375270] (imputed) 3 facial height measurement http://www.ebi.ac.uk/efo/EFO_0007856 GCST90162618 Genome-wide genotyping array 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kunitz-type protease inhibitor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 Kunitz-type protease inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008200 GCST90137588 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Basal Cell Adhesion Molecule levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 basal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008032 GCST90137589 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-6 receptor subunit alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90137590 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. E-selectin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90137591 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. melanoma-derived growth regulatory protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90137592 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-1 receptor antagonist protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90137593 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tissue factor pathway inhibitor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90137594 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cadherin-5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cadherin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008060 GCST90137595 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ficolin-3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ficolin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020392 GCST90137596 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Urokinase plasminogen activator surface receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90137597 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Receptor tyrosine-protein kinase erbB-3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 receptor tyrosine-protein kinase erbb-3 measurement http://www.ebi.ac.uk/efo/EFO_0020701 GCST90137598 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement C2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C2 measurement http://www.ebi.ac.uk/efo/EFO_0020274 GCST90137599 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Phospholipase A2, membrane associated levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90137600 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor ligand superfamily member 11 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90137601 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. GTPase KRas levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 GTPase kras measurement http://www.ebi.ac.uk/efo/EFO_0020432 GCST90137602 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Parathyroid hormone-related protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 parathyroid hormone-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020622 GCST90137603 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Trefoil factor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 trefoil factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0021846 GCST90137604 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Coagulation Factor XI levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 factor XI measurement http://www.ebi.ac.uk/efo/EFO_0004694 GCST90137605 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Pleiotrophin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 pleiotrophin measurement http://www.ebi.ac.uk/efo/EFO_0020651 GCST90137606 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Low affinity immunoglobulin epsilon Fc receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 low affinity immunoglobulin epsilon Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0008210 GCST90137607 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor receptor superfamily member 6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90137608 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. kallikrein-11 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90137609 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. N-terminal pro-BNP levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 N-terminal prohormone brain natriuretic peptide measurement http://www.ebi.ac.uk/efo/EFO_0010921 GCST90137610 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. L-selectin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90137611 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Intercellular adhesion molecule 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST90137612 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. A disintegrin and metalloproteinase with thrombospondin motifs 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90137688 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor ligand superfamily member 8 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90137689 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kunitz-type protease inhibitor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 Kunitz-type protease inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008199 GCST90137690 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Layilin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 layilin measurement http://www.ebi.ac.uk/efo/EFO_0020529 GCST90137691 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Secreted frizzled-related protein 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90137692 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein E (isoform E3) levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 apolipoprotein E (isoform E3) measurement http://www.ebi.ac.uk/efo/EFO_0020157 GCST90137693 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein E (isoform E4) levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 apolipoprotein E (isoform E4) measurement http://www.ebi.ac.uk/efo/EFO_0020158 GCST90137694 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor receptor superfamily member 13C levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor receptor superfamily member 13C measurement http://www.ebi.ac.uk/efo/EFO_0020804 GCST90137695 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cathepsin S levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90137696 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. WNT1-inducible-signaling pathway protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 WNT1-inducible-signaling pathway protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008321 GCST90137697 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leukemia inhibitory factor receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90137698 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Afamin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 afamin measurement http://www.ebi.ac.uk/efo/EFO_0008015 GCST90137699 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein M levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 familial apolipoprotein B hypobetalipoproteinemia http://www.ebi.ac.uk/efo/EFO_1001789 GCST90137700 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. MAP kinase-activated protein kinase 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90137701 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor-inducible gene 6 protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor-inducible gene 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0008311 GCST90137702 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-17 receptor A levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90137703 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Serine/threonine-protein kinase receptor R3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 serine/threonine-protein kinase receptor R3 measurement http://www.ebi.ac.uk/efo/EFO_0020733 GCST90137704 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Programmed cell death 1 ligand 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90137705 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Contactin-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 contactin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020286 GCST90137706 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. GDNF family receptor alpha-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 gdnf family receptor alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020400 GCST90137707 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-18 receptor accessory protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 18 receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008179 GCST90137708 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Programmed cell death 1 ligand 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 programmed cell death 1 ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0008268 GCST90137709 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Carbonic anhydrase 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 carbonic anhydrase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020227 GCST90137710 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor receptor superfamily member EDAR levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 tumor necrosis factor receptor superfamily member EDAR measurement http://www.ebi.ac.uk/efo/EFO_0008310 GCST90137711 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-1 receptor-like 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0008169 GCST90137712 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kallistatin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90137713 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tropomyosin beta chain levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tropomyosin beta chain measurement http://www.ebi.ac.uk/efo/EFO_0020787 GCST90137714 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Insulin-like growth factor-binding protein 7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90137715 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Sex hormone-binding globulin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90137716 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Spondin-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90137717 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Retinoic acid receptor responder protein 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 retinoic acid receptor responder protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008274 GCST90137718 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Teratocarcinoma-derived growth factor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90137719 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. CD209 antigen levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90137720 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Endothelial cell-selective adhesion molecule levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90137721 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Galectin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 galectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020397 GCST90137722 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Galectin-4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 galectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020398 GCST90137723 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Growth hormone receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 growth hormone receptor measurement http://www.ebi.ac.uk/efo/EFO_0020426 GCST90137724 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Intercellular adhesion molecule 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90137725 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. interleukin-17 receptor B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0008176 GCST90137726 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-36 alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin-36 alpha measurement http://www.ebi.ac.uk/efo/EFO_0021851 GCST90137727 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-22 receptor subunit alpha-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 soluble interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0007650 GCST90137728 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-23 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90137729 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-23 receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90137730 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-5 receptor subunit alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008186 GCST90137731 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-7 receptor subunit alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin-7 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020508 GCST90137732 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leukocyte immunoglobulin-like receptor subfamily B member 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90137733 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Limbic system-associated membrane protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 limbic system-associated membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0020537 GCST90137734 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. MHC class I polypeptide-related sequence B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 MHC class I polypeptide-related sequence B measurement http://www.ebi.ac.uk/efo/EFO_0008234 GCST90137735 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Muellerian-inhibiting factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 muellerian-inhibiting factor measurement http://www.ebi.ac.uk/efo/EFO_0020584 GCST90137736 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Natural cytotoxicity triggering receptor 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 natural cytotoxicity triggering receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008243 GCST90137737 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Natural cytotoxicity triggering receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90137738 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Reticulon-4 receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90137739 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor receptor superfamily member 19L levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90137740 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Semaphorin-6A levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90137741 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Myeloid cell surface antigen CD33 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90137742 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Sialic acid-binding Ig-like lectin 6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 sialic acid-binding Ig-like lectin 6 measurement http://www.ebi.ac.uk/efo/EFO_0008285 GCST90137743 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Sialic acid-binding Ig-like lectin 7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90137744 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Sialic acid-binding Ig-like lectin 9 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 sialic acid-binding Ig-like lectin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008286 GCST90137745 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Scavenger receptor class F member 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90137746 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-27 receptor subunit alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 interleukin 27 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008183 GCST90137747 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. alpha-2-macroglobulin receptor-associated protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90137748 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90137749 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Secreted and transmembrane protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 secreted and transmembrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021852 GCST90137750 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. SPARC-like protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90137751 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Gelsolin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 gelsolin measurement http://www.ebi.ac.uk/efo/EFO_0020402 GCST90137752 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Galactoside 3(4)-L-fucosyltransferase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 galactoside 3(4)-L-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0021853 GCST90137753 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. N-acetyl-D-glucosamine kinase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 N-acetyl-D-glucosamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0008239 GCST90137754 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein L1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90137755 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Neurogenic locus notch homolog protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 neurogenic locus notch homolog protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008246 GCST90137756 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Scavenger receptor cysteine-rich type 1 protein M130 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 scavenger receptor cysteine-rich type 1 protein m130 measurement http://www.ebi.ac.uk/efo/EFO_0020717 GCST90137757 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Polymeric immunoglobulin receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90137758 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Chitotriosidase-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90137759 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tyrosine-protein kinase transmembrane receptor ROR1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tyrosine-protein kinase transmembrane receptor ROR1 measurement http://www.ebi.ac.uk/efo/EFO_0020831 GCST90137760 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Trefoil factor 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90137761 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Fatty acid-binding protein, liver levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 fatty acid-binding protein, liver measurement http://www.ebi.ac.uk/efo/EFO_0021855 GCST90137762 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. S-formylglutathione hydrolase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 S-formylglutathione hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0008275 GCST90137763 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Plexin-C1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 plexin-C1 measurement http://www.ebi.ac.uk/efo/EFO_0008266 GCST90137764 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Histidine-rich glycoprotein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 histidine-rich glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008155 GCST90137765 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Hepatocyte growth factor activator levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 hepatocyte growth factor activator measurement http://www.ebi.ac.uk/efo/EFO_0008152 GCST90137766 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Lactadherin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 lactadherin measurement http://www.ebi.ac.uk/efo/EFO_0008203 GCST90137767 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Prolyl endopeptidase FAP levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 prolyl endopeptidase FAP measurement http://www.ebi.ac.uk/efo/EFO_0021856 GCST90137768 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ficolin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 ficolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008135 GCST90137769 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Transforming growth factor-beta-induced protein ig-h3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 transforming growth factor-beta-induced protein ig-h3 measurement http://www.ebi.ac.uk/efo/EFO_0008302 GCST90137770 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Extracellular matrix protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008126 GCST90137771 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. A disintegrin and metalloproteinase with thrombospondin motifs 13 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90137772 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cytoskeleton-associated protein 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 cytoskeleton-associated protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020309 GCST90137773 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Beta-Ala-His dipeptidase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 beta-Ala-His dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0008033 GCST90137774 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Collectin-11 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90137775 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Fetuin-B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 fetuin-B measurement http://www.ebi.ac.uk/efo/EFO_0008128 GCST90137776 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement factor H-related protein 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C5 measurement http://www.ebi.ac.uk/efo/EFO_0020278 GCST90137777 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Agouti-related protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90137778 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Gremlin-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 gremlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020421 GCST90137779 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cystatin-F levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90137780 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Lactoperoxidase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 lactoperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0020525 GCST90137781 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Granulins levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 3 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90137782 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ephrin type-B receptor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90137783 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Thrombospondin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90137784 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Dual specificity mitogen-activated protein kinase kinase 4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 dual specificity mitogen-activated protein kinase kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0008113 GCST90137785 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Protein FAM3B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90137786 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Synaptosomal-associated protein 25 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 synaptosomal-associated protein 25 measurement http://www.ebi.ac.uk/efo/EFO_0021858 GCST90137787 Genome-wide sequencing 2022-09-13 35935937 Hoglund J 2022-07-22 Front Immunol www.ncbi.nlm.nih.gov/pubmed/35935937 Gene-Based Variant Analysis of Whole-Exome Sequencing in Relation to Eosinophil Count. Eosinophil counts 365,954 British ancestry individuals NA Affymetrix [6661079] (imputed) 205 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90134621 Genome-wide genotyping array 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12469) 2,466 Black/admixed ancestry individuals NA Illumina [153771] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178750 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1247) 2,466 Black/admixed ancestry individuals NA Illumina [175768] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176639 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12470) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [161848] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176640 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12471) 2,466 Black/admixed ancestry individuals NA Illumina [176636] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176641 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12472) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153002] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176642 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12481) 2,466 Black/admixed ancestry individuals NA Illumina [150099] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176643 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12488) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152288] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176644 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12489) 2,466 Black/admixed ancestry individuals NA Illumina [153090] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176645 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1249) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [148466] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176646 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12497) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [156633] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176647 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI125) 2,466 Black/admixed ancestry individuals NA Illumina [146529] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176648 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI125) 2,466 Black/admixed ancestry individuals NA Illumina [148284] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178751 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12500) 2,466 Black/admixed ancestry individuals NA Illumina [152084] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176649 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12500) 2,466 Black/admixed ancestry individuals NA Illumina [151056] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178752 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12502) 2,466 Black/admixed ancestry individuals NA Illumina [153290] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176650 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12506) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [170539] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176651 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1251) 2,466 Black/admixed ancestry individuals NA Illumina [161851] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176652 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1251) 2,466 Black/admixed ancestry individuals NA Illumina [147789] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178975 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12554) 2,466 Black/admixed ancestry individuals NA Illumina [158298] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176653 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12565) 2,466 Black/admixed ancestry individuals NA Illumina [141519] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176654 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12566) 2,466 Black/admixed ancestry individuals NA Illumina [174701] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176655 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12568) 2,466 Black/admixed ancestry individuals NA Illumina [185936] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176656 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12568) 2,466 Black/admixed ancestry individuals NA Illumina [153097] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178976 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12573) 2,466 Black/admixed ancestry individuals NA Illumina [162512] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176657 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12576) 2,466 Black/admixed ancestry individuals NA Illumina [166009] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176658 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12577) 2,466 Black/admixed ancestry individuals NA Illumina [156677] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176659 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12583) 2,466 Black/admixed ancestry individuals NA Illumina [152149] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176660 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12605) 2,466 Black/admixed ancestry individuals NA Illumina [156362] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176661 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1261) 2,466 Black/admixed ancestry individuals NA Illumina [160350] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176662 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1264) 2,466 Black/admixed ancestry individuals NA Illumina [156488] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176663 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12663) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [174182] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176664 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12667) 2,466 Black/admixed ancestry individuals NA Illumina [161943] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176665 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12674) 2,466 Black/admixed ancestry individuals NA Illumina [148738] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176666 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12678) 2,466 Black/admixed ancestry individuals NA Illumina [150987] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176667 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12680) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [162846] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176668 Genome-wide sequencing 2022-09-08 35958505 Bhat KG 2022-07-15 Am J Transl Res www.ncbi.nlm.nih.gov/pubmed/35958505 Preliminary genome wide screening identifies new variants associated with coronary artery disease in Indian population. Coronary artery disease 76 Indian ancestry cases, 77 Indian ancestry controls NA Illumina [700000] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90134554 Genome-wide genotyping array 2022-09-21 35927488 Rajagopal VM 2022-08-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35927488 Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder. Attention deficit hyperactivity disorder (childhood) 14,878 Danish ancestry cases, 38,303 Danish ancestry controls NA Illumina [5826893] (imputed) 4 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90137499 Genome-wide genotyping array 2022-09-21 35927488 Rajagopal VM 2022-08-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35927488 Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder. Attention deficit hyperactivity disorder (persistent) 1,473 Danish ancestry cases, 38,303 Danish ancestry controls NA Illumina [5826893] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90137500 Genome-wide genotyping array 2022-09-21 35927488 Rajagopal VM 2022-08-04 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35927488 Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder. Attention deficit hyperactivity disorder (late-diagnosed) 6,961 Danish ancestry cases, 38,303 Danish ancestry controls NA Illumina [5826893] (imputed) 1 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90137501 Genome-wide genotyping array 2022-10-06 34459509 Ken-Dror G 2021-08-30 Ann Neurol www.ncbi.nlm.nih.gov/pubmed/34459509 Genome-wide association study identifies first locus associated with susceptibility to cerebral venous thrombosis. Cerebral venous thrombosis 882 European ancestry cases, 1,205 European ancestry controls NA Illumina [6041026] (imputed) 2 intracranial thrombosis http://purl.obolibrary.org/obo/MONDO_0002907 GCST90038454 Genome-wide genotyping array 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement factor I levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement factor I measurement http://www.ebi.ac.uk/efo/EFO_0008099 GCST90137638 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 14 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 14 measurement http://www.ebi.ac.uk/efo/EFO_0008042 GCST90137639 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Endothelial monocyte-activating polypeptide 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 endothelial monocyte-activating polypeptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020348 GCST90137640 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Chitinase-3-like protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90137641 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Aflatoxin B1 aldehyde reductase member 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 aflatoxin B1 aldehyde reductase member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020132 GCST90137642 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Extracellular superoxide dismutase [Cu-Zn] levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 superoxide dismutase [Cu-Zn] measurement http://www.ebi.ac.uk/efo/EFO_0020758 GCST90137643 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cation-independent mannose-6-phosphate receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90137644 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Galectin-3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90137645 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Neural cell adhesion molecule 1, 120 kDa isoform levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 neural cell adhesion molecule 1, 120 kda isoform measurement http://www.ebi.ac.uk/efo/EFO_0020593 GCST90137646 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Growth/differentiation factor 15 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90137647 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-6 receptor subunit beta levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 interleukin-6 receptor measurement http://www.ebi.ac.uk/efo/EFO_0004814 GCST90137648 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kallikrein-8 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90137649 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kallikrein-12 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kallikrein-12 measurement http://www.ebi.ac.uk/efo/EFO_0008194 GCST90137650 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kallikrein-14 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90137651 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Myeloblastin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90137652 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Carboxypeptidase B2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 carboxypeptidase B2 measurement http://www.ebi.ac.uk/efo/EFO_0008069 GCST90137653 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Endothelin-converting enzyme 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90137654 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Bone morphogenetic protein 7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 bone morphogenetic protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020187 GCST90137655 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tartrate-resistant acid phosphatase type 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90137656 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Insulin receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 insulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008160 GCST90137657 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. CD27 antigen levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 CD27 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008078 GCST90137658 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ephrin type-A receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ephrin type-A receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008123 GCST90137659 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. GDNF family receptor alpha-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 GDNF family receptor alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0008138 GCST90137660 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-1 receptor-like 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 1 receptor-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008168 GCST90137661 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-10 receptor subunit beta levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90137662 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-12 receptor subunit beta-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90137663 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-15 receptor subunit alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 15 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008172 GCST90137664 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. interleukin-18 receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90137665 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Platelet-derived growth factor receptor beta levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90137666 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cadherin-3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cadherin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020213 GCST90137667 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Resistin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90137668 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Granzyme A levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90137669 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Growth/differentiation factor 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 growth/differentiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020429 GCST90137670 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-25 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 25 measurement http://www.ebi.ac.uk/efo/EFO_0008182 GCST90137671 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-19 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 19 measurement http://www.ebi.ac.uk/efo/EFO_0008180 GCST90137672 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 3-like 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 3-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008052 GCST90137673 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 4-like levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 4-like measurement http://www.ebi.ac.uk/efo/EFO_0021848 GCST90137674 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Stem Cell Growth Factor-beta levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 stem Cell Growth Factor beta measurement http://www.ebi.ac.uk/efo/EFO_0008292 GCST90137675 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Dickkopf-related protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90137676 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Elafin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90137677 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Heparin cofactor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 heparin cofactor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008150 GCST90137678 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Protein Z-dependent protease inhibitor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90137679 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interferon alpha/beta receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interferon alpha/beta receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021850 GCST90137680 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Bactericidal permeability-increasing protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 bactericidal permeability-increasing protein measurement http://www.ebi.ac.uk/efo/EFO_0020172 GCST90137681 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Peptidoglycan recognition protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90137682 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Mannose-binding protein C levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 mannose-binding protein C measurement http://www.ebi.ac.uk/efo/EFO_0008224 GCST90137683 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement decay-accelerating factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement decay-accelerating factor measurement http://www.ebi.ac.uk/efo/EFO_0008095 GCST90137684 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Macrophage mannose receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 macrophage mannose receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020548 GCST90137685 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-1 Receptor accessory protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 1 Receptor accessory protein measurement http://www.ebi.ac.uk/efo/EFO_0008167 GCST90137686 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Low-density lipoprotein receptor-related protein 8 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 low-density lipoprotein receptor-related protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0020538 GCST90137687 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Metalloproteinase inhibitor 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 metalloproteinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008231 GCST90137613 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Pigment epithelium-derived factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 pigment epithelium-derived factor measurement http://www.ebi.ac.uk/efo/EFO_0021847 GCST90137614 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 27 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 27 measurement http://www.ebi.ac.uk/efo/EFO_0020198 GCST90137615 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-X-C motif chemokine 6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90137616 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Growth-regulated alpha protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST90137617 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Intercellular adhesion molecule 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90137618 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leptin receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90137619 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 22 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90137620 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 15 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90137621 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Properdin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 properdin measurement http://www.ebi.ac.uk/efo/EFO_0008269 GCST90137622 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 21 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 21 measurement http://www.ebi.ac.uk/efo/EFO_0008048 GCST90137623 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 17 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 C-C motif chemokine 17 measurement http://www.ebi.ac.uk/efo/EFO_0008045 GCST90137624 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 25 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90137625 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tenascin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90137626 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tyrosine-protein kinase receptor Tie-1, soluble levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 tyrosine-protein kinase receptor Tie-1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008312 GCST90137627 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Angiopoietin-1 receptor, soluble levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 angiopoietin-1 receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008023 GCST90137628 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Vascular endothelial growth factor receptor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90137629 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 16 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90137630 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ck-beta-8-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 Ck-beta-8-1 measurement http://www.ebi.ac.uk/efo/EFO_0008085 GCST90137631 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 23 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90137632 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Insulin-like growth factor 1 receptor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 insulin-like growth factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020473 GCST90137633 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Vascular endothelial growth factor receptor 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90137634 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-C motif chemokine 18 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-C motif chemokine 18 measurement http://www.ebi.ac.uk/efo/EFO_0008046 GCST90137635 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Coagulation factor Xa levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 coagulation factor XA measurement http://www.ebi.ac.uk/efo/EFO_0020266 GCST90137636 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-X-C motif chemokine 11 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90137637 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12070) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153244] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176595 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12072) 2,466 Black/admixed ancestry individuals NA Illumina [151801] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176596 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12084) 2,466 Black/admixed ancestry individuals NA Illumina [157132] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176597 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12089) 2,466 Black/admixed ancestry individuals NA Illumina [151126] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176598 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12095) 2,466 Black/admixed ancestry individuals NA Illumina [159743] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176599 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12095) 2,466 Black/admixed ancestry individuals NA Illumina [144600] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178972 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12104) 2,466 Black/admixed ancestry individuals NA Illumina [144891] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176600 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12104) 2,466 Black/admixed ancestry individuals NA Illumina [149902] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178747 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12107) 2,466 Black/admixed ancestry individuals NA Illumina [160029] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176601 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12117) 2,466 Black/admixed ancestry individuals NA Illumina [155391] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176602 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12126) 2,466 Black/admixed ancestry individuals NA Illumina [153316] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176603 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12128) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [152448] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176604 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12147) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [160882] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176605 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12155) 2,466 Black/admixed ancestry individuals NA Illumina [153921] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176606 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12161) 2,466 Black/admixed ancestry individuals NA Illumina [156894] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176607 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12166) 2,466 Black/admixed ancestry individuals NA Illumina [170356] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176608 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12176) 2,466 Black/admixed ancestry individuals NA Illumina [156806] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176609 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12184) 2,466 Black/admixed ancestry individuals NA Illumina [156993] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176610 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12192) 2,466 Black/admixed ancestry individuals NA Illumina [152254] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176611 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12195) 2,466 Black/admixed ancestry individuals NA Illumina [154956] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176612 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12196) 2,466 Black/admixed ancestry individuals NA Illumina [155836] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176613 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12214) 2,466 Black/admixed ancestry individuals NA Illumina [155843] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176614 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12268) 2,466 Black/admixed ancestry individuals NA Illumina [147276] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176615 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1227) 2,466 Black/admixed ancestry individuals NA Illumina [143012] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176616 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12305) 2,466 Black/admixed ancestry individuals NA Illumina [167776] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176617 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12305) 2,466 Black/admixed ancestry individuals NA Illumina [168000] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178748 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12315) 2,466 Black/admixed ancestry individuals NA Illumina [151703] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176618 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12316) 2,466 Black/admixed ancestry individuals NA Illumina [153729] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176619 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12324) 2,466 Black/admixed ancestry individuals NA Illumina [152214] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176620 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12329) 2,466 Black/admixed ancestry individuals NA Illumina [154869] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176621 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1234) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [150668] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176622 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12380) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [151853] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176623 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12383) 2,466 Black/admixed ancestry individuals NA Illumina [163774] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176624 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI1239) 2,466 Black/admixed ancestry individuals NA Illumina [158616] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176625 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12392) 2,466 Black/admixed ancestry individuals NA Illumina [158356] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176626 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12392) 2,466 Black/admixed ancestry individuals NA Illumina [158954] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178973 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12393) 2,466 Black/admixed ancestry individuals NA Illumina [154502] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176627 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12410) 2,466 Black/admixed ancestry individuals NA Illumina [157551] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176628 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12411) 2,466 Black/admixed ancestry individuals NA Illumina [158952] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176629 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12433) 2,466 Black/admixed ancestry individuals NA Illumina [167446] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176630 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12433) 2,466 Black/admixed ancestry individuals NA Illumina [151081] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178974 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12438) 2,466 Black/admixed ancestry individuals NA Illumina [155987] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176631 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12439) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [176082] 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176632 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12448) 2,466 Black/admixed ancestry individuals NA Illumina [155435] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176633 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12452) 2,466 Black/admixed ancestry individuals NA Illumina [146919] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176634 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12455) 2,466 Black/admixed ancestry individuals NA Illumina [155332] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176635 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12466) 2,466 Black/admixed ancestry individuals NA Illumina [163662] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176636 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12467) 2,466 Black/admixed ancestry individuals NA Illumina [160086] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176637 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12467) 2,466 Black/admixed ancestry individuals NA Illumina [152881] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178749 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12469) 2,466 Black/admixed ancestry individuals NA Illumina [153738] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176638 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5460) 2,466 Black/admixed ancestry individuals NA Illumina [155924] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177894 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5461) 2,466 Black/admixed ancestry individuals NA Illumina [150320] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177895 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5465) 2,466 Black/admixed ancestry individuals NA Illumina [164166] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177896 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5465) 2,466 Black/admixed ancestry individuals NA Illumina [141881] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179070 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5468) 2,466 Black/admixed ancestry individuals NA Illumina [172636] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177897 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5469) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [157675] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177898 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI548) 2,466 Black/admixed ancestry individuals NA Illumina [156403] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177899 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5484) 2,466 Black/admixed ancestry individuals NA Illumina [166559] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177900 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5484) 2,466 Black/admixed ancestry individuals NA Illumina [154819] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179071 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5485) 2,466 Black/admixed ancestry individuals NA Illumina [154938] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177901 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5509) 2,466 Black/admixed ancestry individuals NA Illumina [155475] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177902 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5539) 2,466 Black/admixed ancestry individuals NA Illumina [154958] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177903 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5541) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [155648] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177904 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5562) 2,466 Black/admixed ancestry individuals NA Illumina [170765] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177905 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI557) 2,466 Black/admixed ancestry individuals NA Illumina [158076] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177906 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5576) 2,466 Black/admixed ancestry individuals NA Illumina [163410] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177907 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI558) 2,466 Black/admixed ancestry individuals NA Illumina [155960] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177908 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5589) 2,466 Black/admixed ancestry individuals NA Illumina [171085] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177909 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI559) 2,466 Black/admixed ancestry individuals NA Illumina [154283] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177910 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5593) 2,466 Black/admixed ancestry individuals NA Illumina [155716] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177911 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5595) 2,466 Black/admixed ancestry individuals NA Illumina [153124] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177912 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5596) 2,466 Black/admixed ancestry individuals NA Illumina [153058] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177913 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5597) 2,466 Black/admixed ancestry individuals NA Illumina [170501] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179072 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI560) 2,466 Black/admixed ancestry individuals NA Illumina [155225] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177914 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5604) 2,466 Black/admixed ancestry individuals NA Illumina [154124] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177915 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5706) 2,466 Black/admixed ancestry individuals NA Illumina [162399] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177936 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5719) 2,466 Black/admixed ancestry individuals NA Illumina [156938] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177937 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5719) 2,466 Black/admixed ancestry individuals NA Illumina [149159] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178878 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI574) 2,466 Black/admixed ancestry individuals NA Illumina [153502] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177938 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5745) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [173115] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177939 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI575) 2,466 Black/admixed ancestry individuals NA Illumina [156299] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177940 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5751) 2,466 Black/admixed ancestry individuals NA Illumina [151481] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177941 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5751) 2,466 Black/admixed ancestry individuals NA Illumina [145961] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179077 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5755) 2,466 Black/admixed ancestry individuals NA Illumina [190168] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177942 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5755) 2,466 Black/admixed ancestry individuals NA Illumina [165286] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179078 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5758) 2,466 Black/admixed ancestry individuals NA Illumina [160202] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177943 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5758) 2,466 Black/admixed ancestry individuals NA Illumina [157567] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178879 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5762) 2,466 Black/admixed ancestry individuals NA Illumina [156605] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177944 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI577) 2,466 Black/admixed ancestry individuals NA Illumina [177714] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177945 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5780) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [172034] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177946 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5785) 2,466 Black/admixed ancestry individuals NA Illumina [152774] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177947 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5790) 2,466 Black/admixed ancestry individuals NA Illumina [153549] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177948 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI580) 2,466 Black/admixed ancestry individuals NA Illumina [156146] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177949 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5801) 2,466 Black/admixed ancestry individuals NA Illumina [150056] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177950 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5803) 2,466 Black/admixed ancestry individuals NA Illumina [162364] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177951 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5815) 2,466 Black/admixed ancestry individuals NA Illumina [152716] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177952 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5819) 2,466 Black/admixed ancestry individuals NA Illumina [152633] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177953 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI583) 2,466 Black/admixed ancestry individuals NA Illumina [173445] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177954 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI583) 2,466 Black/admixed ancestry individuals NA Illumina [151214] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178880 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5835) 2,466 Black/admixed ancestry individuals NA Illumina [153454] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177955 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6095) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [158852] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178000 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6096) 2,466 Black/admixed ancestry individuals NA Illumina [154832] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178001 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6102) 2,466 Black/admixed ancestry individuals NA Illumina [152060] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178002 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6103) 2,466 Black/admixed ancestry individuals NA Illumina [149723] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178003 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6105) 2,466 Black/admixed ancestry individuals NA Illumina [153539] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178004 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6109) 2,466 Black/admixed ancestry individuals NA Illumina [157476] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178005 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI611) 2,466 Black/admixed ancestry individuals NA Illumina [156989] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178006 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6115) 2,466 Black/admixed ancestry individuals NA Illumina [164021] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178007 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI612) 2,466 Black/admixed ancestry individuals NA Illumina [156142] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178008 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6122) 2,466 Black/admixed ancestry individuals NA Illumina [149604] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178009 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6123) 2,466 Black/admixed ancestry individuals NA Illumina [153636] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178010 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6124) 2,466 Black/admixed ancestry individuals NA Illumina [154142] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178011 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6127) 2,466 Black/admixed ancestry individuals NA Illumina [155477] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178012 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6128) 2,466 Black/admixed ancestry individuals NA Illumina [152712] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178013 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI613) 2,466 Black/admixed ancestry individuals NA Illumina [156892] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178014 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI614) 2,466 Black/admixed ancestry individuals NA Illumina [149084] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178015 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6141) 2,466 Black/admixed ancestry individuals NA Illumina [145400] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178016 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6147) 2,466 Black/admixed ancestry individuals NA Illumina [151784] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178017 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6147) 2,466 Black/admixed ancestry individuals NA Illumina [154478] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178885 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI615) 2,466 Black/admixed ancestry individuals NA Illumina [153996] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178018 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6159) 2,466 Black/admixed ancestry individuals NA Illumina [152860] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178019 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6159) 2,466 Black/admixed ancestry individuals NA Illumina [152008] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178886 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI616) 2,466 Black/admixed ancestry individuals NA Illumina [156805] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178020 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12050) 2,466 Black/admixed ancestry individuals NA Illumina [150680] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176593 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI12064) 2,466 Black/admixed ancestry individuals NA Illumina [155181] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90176594 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5943) 2,466 Black/admixed ancestry individuals NA Illumina [144957] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177977 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5953) 2,466 Black/admixed ancestry individuals NA Illumina [157667] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177978 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI596) 2,466 Black/admixed ancestry individuals NA Illumina [154115] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177979 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5963) 2,466 Black/admixed ancestry individuals NA Illumina [143790] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177980 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI5963) 2,466 Black/admixed ancestry individuals NA Illumina [185810] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90179080 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI597) 2,466 Black/admixed ancestry individuals NA Illumina [154744] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177981 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI598) 2,466 Black/admixed ancestry individuals NA Illumina [152897] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177982 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI601) 2,466 Black/admixed ancestry individuals NA Illumina [158113] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177983 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI601) 2,466 Black/admixed ancestry individuals NA Illumina [156637] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90178884 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6015) 2,466 Black/admixed ancestry individuals NA Illumina [149353] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177984 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6044) 2,466 Black/admixed ancestry individuals NA Illumina [157397] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177985 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6046) 2,466 Black/admixed ancestry individuals NA Illumina [160920] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177986 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI605) 2,466 Black/admixed ancestry individuals NA Illumina [155712] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177987 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6054) 2,466 Black/admixed ancestry individuals NA Illumina [153549] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177988 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6055) 2,466 Black/admixed ancestry individuals NA Illumina [167860] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177989 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6058) 2,466 Black/admixed ancestry individuals NA Illumina [155879] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177990 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6062) 2,466 Black/admixed ancestry individuals NA Illumina [151231] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177991 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6066) 2,466 Black/admixed ancestry individuals NA Illumina [154638] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177992 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6069) 2,466 Black/admixed ancestry individuals NA Illumina [156355] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177993 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI607) 2,466 Black/admixed ancestry individuals NA Illumina [149824] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177994 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6072) 2,466 Black/admixed ancestry individuals NA Illumina [150380] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177995 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6080) 2,466 Black/admixed ancestry individuals up to 1,653 European, Hispanic, Asian or Black individuals Illumina [153736] 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177996 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI609) 2,466 Black/admixed ancestry individuals NA Illumina [141960] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177997 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6091) 2,466 Black/admixed ancestry individuals NA Illumina [150339] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177998 Genome-wide sequencing 2022-11-17 35995766 Tahir UA 2022-08-22 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35995766 Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Metabolite peak levels (QI6093) 2,466 Black/admixed ancestry individuals NA Illumina [157319] 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90177999 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. SLAM family member 7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90137888 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leucine-rich repeat serine/threonine-protein kinase 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leucine-rich repeat serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0021876 GCST90137889 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kininogen-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kininogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008198 GCST90137890 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Platelet receptor Gi24 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 platelet receptor Gi24 measurement http://www.ebi.ac.uk/efo/EFO_0021877 GCST90137891 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. R-spondin-3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 r-spondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0021878 GCST90137892 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Immunoglobulin superfamily containing leucine-rich repeat protein 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 immunoglobulin superfamily containing leucine-rich repeat protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021879 GCST90137893 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Toll-like receptor 4:Lymphocyte antigen 96 complex levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90137894 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Quinone oxidoreductase-like protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 quinone oxidoreductase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021880 GCST90137895 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ubiquitin carboxyl-terminal hydrolase 25 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ubiquitin carboxyl-terminal hydrolase 25 measurement http://www.ebi.ac.uk/efo/EFO_0021881 GCST90137896 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Proprotein convertase subtilisin/kexin type 9 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90137897 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Natural killer cell receptor 2B4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 natural killer cell receptor 2B4 measurement http://www.ebi.ac.uk/efo/EFO_0021882 GCST90137898 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Bone morphogenetic protein 10 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 bone morphogenetic protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020185 GCST90137899 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Insulin-like growth factor-binding protein 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 insulin-like growth factor-binding protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020477 GCST90137900 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Hepatocyte growth factor-like protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90137901 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Aminoacylase-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 aminoacylase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020141 GCST90137902 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cyclin-dependent kinase inhibitor 1B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cyclin-dependent kinase inhibitor 1b measurement http://www.ebi.ac.uk/efo/EFO_0020298 GCST90137903 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Inter-alpha-trypsin inhibitor heavy chain H4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 inter-alpha-trypsin inhibitor heavy chain h4 measurement http://www.ebi.ac.uk/efo/EFO_0020481 GCST90137904 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. T-lymphocyte activation antigen CD86 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 t-lymphocyte activation antigen CD86 measurement http://www.ebi.ac.uk/efo/EFO_0020762 GCST90137905 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Connective tissue growth factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 connective tissue growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020284 GCST90137906 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Betacellulin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 betacellulin measurement http://www.ebi.ac.uk/efo/EFO_0021883 GCST90137907 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Thrombin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 thrombin measurement http://www.ebi.ac.uk/efo/EFO_0020768 GCST90137908 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Plasma serine protease inhibitor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 plasma serine protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0020642 GCST90137909 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement component C6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement component C6 measurement http://www.ebi.ac.uk/efo/EFO_0020281 GCST90137910 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. MHC class I polypeptide-related sequence A levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST90137911 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C34 gp41 HIV Fragment levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 gp41 C34 peptide, HIV measurement http://www.ebi.ac.uk/efo/EFO_0008140 GCST90137912 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Platelet glycoprotein 4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 platelet glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008262 GCST90137913 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Transgelin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 transgelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021884 GCST90137914 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Galectin-3-binding protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 galectin-3-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010241 GCST90137915 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement C5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C5 measurement http://www.ebi.ac.uk/efo/EFO_0020278 GCST90137916 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Semaphorin-6B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 semaphorin-6B measurement http://www.ebi.ac.uk/efo/EFO_0021885 GCST90137917 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement component C8 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement component C8 measurement http://www.ebi.ac.uk/efo/EFO_0008094 GCST90137918 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tumor necrosis factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90137919 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. E3 ubiquitin-protein ligase RNF43 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 e3 ubiquitin-protein ligase RNF43 measurement http://www.ebi.ac.uk/efo/EFO_0021886 GCST90137920 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Glial cell line-derived neurotrophic factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 glial cell line-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0021887 GCST90137921 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-18-binding protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin-18-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020495 GCST90137922 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement C1r subcomponent levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C1r subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008090 GCST90137923 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0021888 GCST90137924 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. N-acetylglucosamine-6-sulfatase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90137925 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Lumican levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 lumican measurement http://www.ebi.ac.uk/efo/EFO_0021889 GCST90137926 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Phosphatidylethanolamine-binding protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 phosphatidylethanolamine-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020634 GCST90137927 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Coagulation Factor VII levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST90137928 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. alpha-1-antichymotrypsin complex levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 alpha-1-antichymotrypsin complex measurement http://www.ebi.ac.uk/efo/EFO_0008018 GCST90137929 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. dCTP pyrophosphatase 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 DCTP pyrophosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020314 GCST90137930 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. 72 kDa type IV collagenase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 72 kda type IV collagenase measurement http://www.ebi.ac.uk/efo/EFO_0020122 GCST90137931 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Apolipoprotein A-I levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 apolipoprotein A 1 measurement http://www.ebi.ac.uk/efo/EFO_0004614 GCST90137932 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cadherin-6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cadherin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020214 GCST90137933 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-10 receptor subunit alpha levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin-10 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0021890 GCST90137934 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Protein disulfide-isomerase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 protein disulfide-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020669 GCST90137935 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. HemK methyltransferase family member 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 hemK methyltransferase family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0021891 GCST90137936 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Complement C3d fragment levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 complement C3D fragment measurement http://www.ebi.ac.uk/efo/EFO_0020277 GCST90137937 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Netrin-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 netrin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020592 GCST90137863 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Neurexophilin-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90137864 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Glypican-5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 glypican-5 measurement http://www.ebi.ac.uk/efo/EFO_0008139 GCST90137865 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cerebral dopamine neurotrophic factor levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90137866 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Killer cell immunoglobulin-like receptor 2DL4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90137867 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Acid sphingomyelinase-like phosphodiesterase 3a levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90137868 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Protein FAM3D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 3 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90137869 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cysteine-rich with EGF-like domain protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 cysteine-rich with EGF-like domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021870 GCST90137870 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Glypican-6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 glypican-6 measurement http://www.ebi.ac.uk/efo/EFO_0021871 GCST90137871 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Non-histone chromosomal protein HMG-14 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 non-histone chromosomal protein HMG-14 measurement http://www.ebi.ac.uk/efo/EFO_0021872 GCST90137872 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Low-density lipoprotein receptor-related protein 1B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 low-density lipoprotein receptor-related protein 1B measurement http://www.ebi.ac.uk/efo/EFO_0021873 GCST90137873 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Peptidyl-prolyl cis-trans isomerase E levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 peptidyl-prolyl cis-trans isomerase E measurement http://www.ebi.ac.uk/efo/EFO_0008257 GCST90137874 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Kynureninase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 kynureninase measurement http://www.ebi.ac.uk/efo/EFO_0008201 GCST90137875 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Alpha-(1,3)-fucosyltransferase 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 alpha-(1,3)-fucosyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020136 GCST90137876 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ectonucleoside triphosphate diphosphohydrolase 5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90137877 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Proprotein convertase subtilisin/kexin type 7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90137878 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Fc receptor-like protein 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 Fc receptor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008127 GCST90137879 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cell adhesion molecule-related/down-regulated by oncogenes levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cell adhesion molecule-related/down-regulated by oncogenes measurement http://www.ebi.ac.uk/efo/EFO_0008079 GCST90137880 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. SLAM family member 6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 SLAM family member 6 measurement http://www.ebi.ac.uk/efo/EFO_0020742 GCST90137881 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. OX-2 membrane glycoprotein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 OX-2 membrane glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008253 GCST90137882 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. CMRF35-like molecule 6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90137883 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cell surface glycoprotein CD200 receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cell surface glycoprotein CD200 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020253 GCST90137884 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ankyrin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ankyrin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021874 GCST90137885 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ubiquitin-like protein ISG15 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ubiquitin-like protein ISG15 measurement http://www.ebi.ac.uk/efo/EFO_0021875 GCST90137886 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Thioredoxin domain-containing protein 12 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90137887 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cystatin-SA levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cystatin-SA measurement http://www.ebi.ac.uk/efo/EFO_0008105 GCST90137813 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Semaphorin-5A levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 semaphorin-5A measurement http://www.ebi.ac.uk/efo/EFO_0021864 GCST90137814 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Trefoil factor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 trefoil factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021865 GCST90137815 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Low affinity immunoglobulin gamma Fc region receptor III-B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 low affinity immunoglobulin gamma Fc region receptor III-B measurement http://www.ebi.ac.uk/efo/EFO_0008212 GCST90137816 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. N-acylethanolamine-hydrolyzing acid amidase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90137817 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Contactin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90137818 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90137819 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Platelet glycoprotein VI levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 platelet glycoprotein VI measurement http://www.ebi.ac.uk/efo/EFO_0008263 GCST90137820 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. CD109 antigen levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 CD109 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008076 GCST90137821 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. CD177 antigen levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cD177 antigen measurement http://www.ebi.ac.uk/efo/EFO_0021866 GCST90137822 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Arylsulfatase B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 arylsulfatase B measurement http://www.ebi.ac.uk/efo/EFO_0008030 GCST90137823 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tyrosine-protein phosphatase non-receptor type substrate 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90137824 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0020344 GCST90137825 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Brevican core protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 brevican core protein measurement http://www.ebi.ac.uk/efo/EFO_0020193 GCST90137826 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Lysosomal protective protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90137827 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Plexin-B2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 plexin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0021867 GCST90137828 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Carbonic anhydrase 6 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 carbonic anhydrase 6 measurement http://www.ebi.ac.uk/efo/EFO_0008068 GCST90137829 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Mediator of RNA polymerase II transcription subunit 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90137830 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Alpha-L-iduronidase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90137831 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Carbonic anhydrase 4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 carbonic anhydrase 4 measurement http://www.ebi.ac.uk/efo/EFO_0020230 GCST90137832 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Neutral ceramidase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90137833 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Proto-oncogene tyrosine-protein kinase receptor Ret levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 proto-oncogene tyrosine-protein kinase receptor Ret measurement http://www.ebi.ac.uk/efo/EFO_0008272 GCST90137834 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Semaphorin-3A levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90137835 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Trypsin-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 trypsin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008305 GCST90137836 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90137837 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. CD48 antigen levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 CD48 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020247 GCST90137838 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Contactin-4 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 contactin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020287 GCST90137839 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Contactin-5 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 contactin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008101 GCST90137840 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cystatin-SN levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cystatin-SN measurement http://www.ebi.ac.uk/efo/EFO_0008106 GCST90137841 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Low affinity immunoglobulin gamma Fc region receptor II-a levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 low affinity immunoglobulin gamma Fc region receptor II-a/b measurement http://www.ebi.ac.uk/efo/EFO_0008211 GCST90137842 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Low affinity immunoglobulin gamma Fc region receptor II-b levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 low affinity immunoglobulin gamma Fc region receptor II-a/b measurement http://www.ebi.ac.uk/efo/EFO_0008211 GCST90137843 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. High affinity immunoglobulin gamma Fc receptor I levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 high affinity immunoglobulin gamma fc receptor i measurement http://www.ebi.ac.uk/efo/EFO_0020447 GCST90137844 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Ficolin-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90137845 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leucine-rich repeats and immunoglobulin-like domains protein 3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leucine-rich repeats and immunoglobulin-like domains protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020534 GCST90137846 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Semaphorin-3E levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90137847 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Testican-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 testican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020766 GCST90137848 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Calcium/calmodulin-dependent protein kinase type 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 calcium/calmodulin-dependent protein kinase type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008062 GCST90137849 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Calcium/calmodulin-dependent protein kinase type 1D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90137850 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Dual specificity mitogen-activated protein kinase kinase 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 dual specificity mitogen-activated protein kinase kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008112 GCST90137851 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Mitogen-activated protein kinase 8 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 mitogen-activated protein kinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020580 GCST90137852 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Serine/threonine-protein kinase 16 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 serine/threonine-protein kinase 16 measurement http://www.ebi.ac.uk/efo/EFO_0020724 GCST90137853 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tyrosine-protein kinase ZAP-70 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tyrosine-protein kinase ZAP-70 measurement http://www.ebi.ac.uk/efo/EFO_0020833 GCST90137854 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-17 receptor D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin 17 receptor D measurement http://www.ebi.ac.uk/efo/EFO_0008177 GCST90137855 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Tryptase beta-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90137856 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Mannan-binding lectin serine protease 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90137857 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Persulfide dioxygenase ETHE1, mitochondrial levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 persulfide dioxygenase ETHE1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008258 GCST90137858 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Acidic leucine-rich nuclear phosphoprotein 32 family member B levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 acidic leucine-rich nuclear phosphoprotein 32 family member b measurement http://www.ebi.ac.uk/efo/EFO_0020125 GCST90137859 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leucine carboxyl methyltransferase 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leucine carboxyl methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008207 GCST90137860 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Copine-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90137861 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. SPARC-related modular calcium-binding protein 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 sPARC-related modular calcium-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021868 GCST90137862 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Oxidized low-density lipoprotein receptor 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 oxidized low-density lipoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020620 GCST90137788 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Peptidyl-prolyl cis-trans isomerase D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 peptidyl-prolyl cis-trans isomerase D measurement http://www.ebi.ac.uk/efo/EFO_0008256 GCST90137789 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Transmembrane glycoprotein NMB levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90137790 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Collectin-12 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90137791 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Carbohydrate sulfotransferase 15 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90137792 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Hepatitis A virus cellular receptor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90137793 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Interleukin-12 receptor subunit beta-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 interleukin-12 receptor subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020492 GCST90137794 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. T-lymphocyte surface antigen Ly-9 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 T-lymphocyte surface antigen Ly-9 measurement http://www.ebi.ac.uk/efo/EFO_0008295 GCST90137795 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Endoplasmic reticulum aminopeptidase 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90137796 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Alcohol dehydrogenase [NADP(+)] levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 alcohol dehydrogenase [NADP+] measurement http://www.ebi.ac.uk/efo/EFO_0008017 GCST90137797 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Low molecular weight phosphotyrosine protein phosphatase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90137798 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Phosphoglucomutase-1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 phosphoglucomutase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021859 GCST90137799 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Macrophage-capping protein levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 macrophage-capping protein measurement http://www.ebi.ac.uk/efo/EFO_0020549 GCST90137800 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Malate dehydrogenase, cytoplasmic levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 malate dehydrogenase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020551 GCST90137801 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Proteasome activator complex subunit 1 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90137802 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Dermatopontin levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90137803 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Nidogen-2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 2 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90137804 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leucine-rich repeat transmembrane protein FLRT2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leucine-rich repeat transmembrane protein FLRT2 measurement http://www.ebi.ac.uk/efo/EFO_0021860 GCST90137805 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Leucine-rich repeat transmembrane protein FLRT3 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90137806 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cathepsin Z levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cathepsin Z measurement http://www.ebi.ac.uk/efo/EFO_0008074 GCST90137807 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cathepsin F levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90137808 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Cystatin-D levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90137809 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. C-type mannose receptor 2 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 C-type mannose receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020204 GCST90137810 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. 3-hydroxyanthranilate 3,4-dioxygenase levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 3-hydroxyanthranilate 3,4-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0021862 GCST90137811 Genome-wide sequencing 2022-09-27 34814699 Katz DH 2021-11-24 Circulation www.ncbi.nlm.nih.gov/pubmed/34814699 Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights Into Cardiovascular Disease. Galectin-9 levels 1,852 African American or Afro-Caribbean individuals 1,688 African American or Afro-Caribbean, Hispanic or Latin American, Asian ancestry, European ancestry individuals Illumina [NR] 1 galectin-9 measurement http://www.ebi.ac.uk/efo/EFO_0021863 GCST90137812 Genome-wide sequencing 2023-11-14 37686257 Llucia-Carol L 2023-08-30 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37686257 Genetic Architecture of Ischaemic Strokes after COVID-19 Shows Similarities with Large Vessel Strokes. Ischemic stroke after COVID-19 73 European ancestry cases, 701 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 0 Ischemic stroke, COVID-19 http://purl.obolibrary.org/obo/HP_0002140, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90297536 Genome-wide genotyping array 2022-09-28 36089080 Chang X 2022-09-08 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/36089080 Genetic architecture of asthma in African American Patients. Asthma 2,638 African American cases, 1,544 African American controls NA Illumina [13374286] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90131434 Genome-wide genotyping array 2022-09-28 36089080 Chang X 2022-09-08 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/36089080 Genetic architecture of asthma in African American Patients. Asthma 3,876 African American cases, 2,607 African American controls NA Illumina [11816366] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90131435 Genome-wide genotyping array 2022-09-28 36089080 Chang X 2022-09-08 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/36089080 Genetic architecture of asthma in African American Patients. Asthma 461 African American cases, 278 African American controls NA Illumina [14110978] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90131436 Genome-wide genotyping array 2022-09-28 36089080 Chang X 2022-09-08 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/36089080 Genetic architecture of asthma in African American Patients. Asthma 6,975 African American cases, 4,429 African American controls NA Illumina [NR] (imputed) 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90139387 Genome-wide genotyping array 2022-09-28 36089080 Chang X 2022-09-08 J Allergy Clin Immunol www.ncbi.nlm.nih.gov/pubmed/36089080 Genetic architecture of asthma in African American Patients. Asthma 10,761 African American cases, 8,867 African American controls NA Illumina [NR] (imputed) 12 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90139388 Genome-wide genotyping array 2022-09-28 35975136 Bortsov AV 2022-08-09 Pain Rep www.ncbi.nlm.nih.gov/pubmed/35975136 Brain-specific genes contribute to chronic but not to acute back pain. Chronic back pain 70,633 European ancestry cases, 304,525 European ancestry controls 19,760 European ancestry cases, 28,674 European ancestry controls Affymetrix [7634838] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90140965 Genome-wide genotyping array 2022-09-28 35975136 Bortsov AV 2022-08-09 Pain Rep www.ncbi.nlm.nih.gov/pubmed/35975136 Brain-specific genes contribute to chronic but not to acute back pain. Acute back pain 32,209 European ancestry cases, 304,525 European ancestry controls 4,379 European ancestry cases, 11,309 European ancestry controls Affymetrix [7635120] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90140966 Genome-wide genotyping array 2022-09-27 33517887 Lopez de Maturana E 2021-02-01 Genome Med www.ncbi.nlm.nih.gov/pubmed/33517887 A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer. Pancreatic cancer 1,317 European ancestry cases, 700 European ancestry controls NA Illumina [317270] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90011857 Genome-wide genotyping array 2022-09-27 33517887 Lopez de Maturana E 2021-02-01 Genome Med www.ncbi.nlm.nih.gov/pubmed/33517887 A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer. Pancreatic cancer 1,317 European ancestry cases, 1,616 European ancestry controls 9,040 cases, 12,496 controls Illumina [315942] (imputed) 1 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90011858 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Uveitis 2,616 European ancestry cases, 478,126 European ancestry controls, 125 East Asian ancestry cases, 174,600 East Asian ancestry controls NA Affymetrix, Illumina [25844095] (imputed) 5 uveitis http://www.ebi.ac.uk/efo/EFO_1001231 GCST90018938 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Varicose veins 22,037 European ancestry cases, 437,665 European ancestry controls, 474 East Asian ancestry cases, 178,252 East Asian ancestry controls NA Affymetrix, Illumina [25842955] (imputed) 71 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90018939 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Ventricular arrhythmia 1,018 European ancestry cases, 327,198 European ancestry controls, 1,673 East Asian ancestry cases, 155,540 East Asian ancestry controls NA Affymetrix, Illumina [20454847] (imputed) 1 Ventricular arrhythmia http://purl.obolibrary.org/obo/HP_0004308 GCST90018940 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Zoster infection 522 European ancestry cases, 351,740 European ancestry controls, 2,209 East Asian ancestry cases, 166,603 East Asian ancestry controls NA Affymetrix, Illumina [20457058] (imputed) 1 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST90018941 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum alkaline phosphatase levels 344,292 European ancestry individuals, 118,886 East Asian ancestry individuals NA Affymetrix, Illumina [20533886] (imputed) 337 alkaline phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0004533 GCST90018942 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Alanine aminotransferase levels 344,136 European ancestry individuals, 150,545 East Asian ancestry individuals NA Affymetrix, Illumina [20538387] (imputed) 248 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90018943 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Aspartate aminotransferase levels 342,990 European ancestry individuals, 150,068 East Asian ancestry individuals NA Affymetrix, Illumina [20538469] (imputed) 286 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90018944 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum albumin levels 315,268 European ancestry individuals, 120,539 East Asian ancestry individuals NA Affymetrix, Illumina [20534035] (imputed) 250 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90018945 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Basophil count 349,856 European ancestry individuals, 91,908 East Asian ancestry individuals NA Affymetrix, Illumina [20529536] (imputed) 71 basophil count http://www.ebi.ac.uk/efo/EFO_0005090 GCST90018946 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Body mass index 359,983 European ancestry individuals, 163,835 East Asian ancestry individuals NA Affymetrix, Illumina [20538802] (imputed) 535 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90018947 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Blood urea nitrogen levels 344,052 European ancestry individuals, 148,767 East Asian ancestry individuals NA Affymetrix, Illumina [20538307] (imputed) 224 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST90018948 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Weight 360,116 European ancestry individuals, 165,419 East Asian ancestry individuals NA Affymetrix, Illumina [20539548] (imputed) 609 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90018949 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. C-reactive protein 353,466 European ancestry individuals, 83,025 East Asian ancestry individuals NA Affymetrix, Illumina [20529698] (imputed) 212 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90018950 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Calcium levels 315,153 European ancestry individuals, 83,980 East Asian ancestry individuals NA Affymetrix, Illumina [20528270] (imputed) 223 calcium measurement http://www.ebi.ac.uk/efo/EFO_0004838 GCST90018951 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Diastolic blood pressure 340,162 European ancestry individuals, 145,515 East Asian ancestry individuals NA Affymetrix, Illumina [20537302] (imputed) 244 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90018952 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Eosinophil counts 349,856 European ancestry individuals, 93,063 East Asian ancestry individuals NA Affymetrix, Illumina [20529668] (imputed) 324 eosinophil count http://www.ebi.ac.uk/efo/EFO_0004842 GCST90018953 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Gamma glutamyl transpeptidase 344,104 European ancestry individuals, 133,471 East Asian ancestry individuals NA Affymetrix, Illumina [20535691] (imputed) 322 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90018954 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Glucose levels 314,916 European ancestry individuals, 133,336 East Asian ancestry individuals NA Affymetrix, Illumina [20535873] (imputed) 117 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90018955 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. HDL cholesterol 315,133 European ancestry individuals, 74,970 East Asian ancestry individuals NA Affymetrix, Illumina [20525311] (imputed) 284 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90018956 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hemoglobin 350,474 European ancestry individuals, 152,447 East Asian ancestry individuals NA Affymetrix, Illumina [20538521] (imputed) 353 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90018957 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hemoglobin A1c levels 344,182 European ancestry individuals, 71,221 East Asian ancestry individuals NA Affymetrix, Illumina [20525742] (imputed) 352 hemoglobin A1 measurement http://www.ebi.ac.uk/efo/EFO_0007629 GCST90018958 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Height 360,388 European ancestry individuals, 165,056 East Asian ancestry individuals NA Affymetrix, Illumina [20538915] (imputed) 723 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90018959 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Hematocrit 350,475 European ancestry individuals, 153,015 East Asian ancestry individuals NA Affymetrix, Illumina [20538534] (imputed) 333 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90018960 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. LDL cholesterol 343,621 European ancestry individuals, 72,866 East Asian ancestry individuals NA Affymetrix, Illumina [20521447] (imputed) 165 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90018961 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Lymphocyte count 349,856 European ancestry individuals, 95,717 East Asian ancestry individuals NA Affymetrix, Illumina [20531022] (imputed) 401 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90018962 Genome-wide genotyping array 2023-02-24 36399516 Garrett ME 2022-11-18 Blood Adv www.ncbi.nlm.nih.gov/pubmed/36399516 Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy. Proteinuria 1,078 individuals NA Illumina [2887736] (imputed) 3 Proteinuria http://purl.obolibrary.org/obo/HP_0000093 GCST90250893 Genome-wide genotyping array 2023-02-24 36399516 Garrett ME 2022-11-18 Blood Adv www.ncbi.nlm.nih.gov/pubmed/36399516 Genome-wide meta-analysis identifies new candidate genes for sickle cell disease nephropathy. Estimated glomerular filtration rate 1,078 individuals NA Illumina [2887736] (imputed) 3 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90250894 Genome-wide genotyping array 2022-08-18 35613103 Huang RDL 2022-05-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/35613103 Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program. Ideal cardiovascular health score (clinical and behavioral) 119,129 European ancestry individuals, 16,495 African American individuals, 6,780 Hispanic individuals 37,646 European ancestry individuals, 5,366 African American individuals, 2,754 Hispanic individuals Affymetrix [29000000] (imputed) 17 clinical and behavioural ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0007654 GCST90132287 Genome-wide genotyping array 2022-08-18 35613103 Huang RDL 2022-05-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/35613103 Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program. Ideal cardiovascular health (clinical and behavioral) 6,018 European, African American or Hispanic cases, 136,386 European, African American or Hispanic controls NA Affymetrix [29000000] (imputed) 16 clinical and behavioural ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0007654 GCST90132291 Genome-wide genotyping array 2022-08-18 35613103 Huang RDL 2022-05-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/35613103 Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program. Ideal cardiovascular health score (clinical) 119,129 European ancestry individuals, 16,495 African American individuals, 6,780 Hispanic individuals NA Affymetrix [29000000] (imputed) 49 clinical ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0007653 GCST90132292 Genome-wide genotyping array 2022-08-18 35613103 Huang RDL 2022-05-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/35613103 Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program. Ideal cardiovascular health (clinical) 6,018 European, African American or Hispanic cases, 136,386 European, African American or Hispanic controls NA Affymetrix [29000000] (imputed) 16 clinical ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0007653 GCST90132293 Genome-wide genotyping array 2022-08-18 35613103 Huang RDL 2022-05-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/35613103 Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program. Ideal cardiovascular health score (behavioral) 119,129 European ancestry individuals, 16,495 African American individuals, 6,780 Hispanic individuals NA Affymetrix [29000000] (imputed) 18 behavioural ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0021791 GCST90132294 Genome-wide genotyping array 2022-08-18 35613103 Huang RDL 2022-05-25 PLoS One www.ncbi.nlm.nih.gov/pubmed/35613103 Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program. Ideal cardiovascular health (behavioral) 6,018 European, African American or Hispanic cases, 136,386 European, African American or Hispanic controls NA Affymetrix [29000000] (imputed) 4 behavioural ideal cardiovascular health http://www.ebi.ac.uk/efo/EFO_0021791 GCST90132295 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. 2,4,5-trichlorophenol levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 2,4,5-trichlorophenol measurement http://www.ebi.ac.uk/efo/EFO_0022052 GCST90165218 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. 2,4,5-trichlorophenol-2 levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 2,4,5-trichlorophenol measurement http://www.ebi.ac.uk/efo/EFO_0022052 GCST90165219 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. 4,6-dinitro-o-cresol levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 4,6-dinitro-o-cresol measurement http://www.ebi.ac.uk/efo/EFO_0022053 GCST90165220 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (AC50 high) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165221 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (AC50 low) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165222 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Aldrin levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 aldrin measurement http://www.ebi.ac.uk/efo/EFO_0022054 GCST90165223 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Azinphos methyl levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 azinphos methyl measurement http://www.ebi.ac.uk/efo/EFO_0022055 GCST90165224 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Cadmium chloride levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 cadmium chloride measurement http://www.ebi.ac.uk/efo/EFO_0022056 GCST90165225 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Chlorpyrifos levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 chlorpyrifos measurement http://www.ebi.ac.uk/efo/EFO_0022057 GCST90165226 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Cobalt levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 blood cobalt measurement http://www.ebi.ac.uk/efo/EFO_0007577 GCST90165227 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. DDT metabolite (DDD p-p') levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 DDT metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007886 GCST90165228 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. DDT metabolite (DDT o-p') levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 DDT metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007886 GCST90165229 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. DDT metabolite (DDT p-p') levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 DDT metabolite measurement http://www.ebi.ac.uk/efo/EFO_0007886 GCST90165230 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Di-n-butyl phthalate levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 dibutyl phthalate measurement http://www.ebi.ac.uk/efo/EFO_0022058 GCST90165231 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Diazinon levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 diazinon measurement http://www.ebi.ac.uk/efo/EFO_0022059 GCST90165232 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Dicofol levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 dicofol measurement http://www.ebi.ac.uk/efo/EFO_0022060 GCST90165233 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Dieldrin levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 dieldrin measurement http://www.ebi.ac.uk/efo/EFO_0022061 GCST90165234 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Disulfoton levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 disulfoton measurement http://www.ebi.ac.uk/efo/EFO_0022062 GCST90165235 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Endosulfan levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 endosulfan measurement http://www.ebi.ac.uk/efo/EFO_0022063 GCST90165236 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Endrin levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 endrin measurement http://www.ebi.ac.uk/efo/EFO_0022064 GCST90165237 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Ethion levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 ethion measurement http://www.ebi.ac.uk/efo/EFO_0022065 GCST90165238 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (Expo high) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165239 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Environmental pollutants exposure (Expo low) 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 environmental exposure measurement http://www.ebi.ac.uk/efo/EFO_0008360 GCST90165240 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Heptachlor levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 heptachlor measurement http://www.ebi.ac.uk/efo/EFO_0022066 GCST90165241 Genome-wide genotyping array 2023-01-05 36006120 Ford LC 2022-08-01 Toxics www.ncbi.nlm.nih.gov/pubmed/36006120 A Population-Based Human In Vitro Approach to Quantify Inter-Individual Variability in Responses to Chemical Mixtures. Heptachlor epoxide levels 146 European ancestry, Sub-Saharan African ancestry lymphoblastoid cell lines NA NR [NR] 66 heptachlor epoxide measurement http://www.ebi.ac.uk/efo/EFO_0022067 GCST90165242 Genome-wide genotyping array 2022-09-15 35977442 Bracher-Smith M 2022-07-29 Neurobiol Aging www.ncbi.nlm.nih.gov/pubmed/35977442 Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis. Alzheimer's disease in APOE E4 homozygosity 288 British ancestry cases, 5,102 British ancestry controls NA Affymetrix [5349830] (imputed) 1 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90134645 Genome-wide genotyping array 2022-08-16 35552711 Pankratz N 2022-05-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35552711 Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Fibrinogen levels 10,118 European ancestry individuals, 3,520 African American individuals NA Illumina [269877] 13 fibrinogen measurement http://www.ebi.ac.uk/efo/EFO_0004623 GCST90132196 Exome-wide sequencing 2022-08-16 35552711 Pankratz N 2022-05-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35552711 Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Factor VII levels 8,403 European ancestry individuals, 3,246 African American individuals NA Illumina [269877] 11 factor VII measurement http://www.ebi.ac.uk/efo/EFO_0004619 GCST90132197 Exome-wide sequencing 2022-08-16 35552711 Pankratz N 2022-05-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35552711 Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. Factor VIII levels 8,580 European ancestry individuals, 11,837 African American individuals NA Illumina [269877] 12 factor VIII measurement http://www.ebi.ac.uk/efo/EFO_0004630 GCST90132198 Exome-wide sequencing 2022-08-16 35552711 Pankratz N 2022-05-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35552711 Whole exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors. von Willebrand factor levels 8,318 European ancestry individuals, 11,421 African American individuals NA Illumina [269877] 10 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90132199 Exome-wide sequencing 2023-02-23 36726022 Sliz E 2023-02-01 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36726022 Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata. Uterine leiomyomata 38,466 European ancestry cases, 329,437 European ancestry controls NA NR [8916581] (imputed) 71 Uterine leiomyoma http://purl.obolibrary.org/obo/HP_0000131 GCST90239856 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean arterial pressure 360,863 European ancestry individuals, 145,502 East Asian ancestry individuals NA Affymetrix, Illumina [20537389] (imputed) 241 mean arterial pressure http://www.ebi.ac.uk/efo/EFO_0006340 GCST90018963 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean corpuscular hemoglobin 350,472 European ancestry individuals, 128,028 East Asian ancestry individuals NA Affymetrix, Illumina [20535878] (imputed) 381 mean corpuscular hemoglobin http://www.ebi.ac.uk/efo/EFO_0004527 GCST90018964 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean corpuscular hemoglobin concentration 350,468 European ancestry individuals, 135,482 East Asian ancestry individuals NA Affymetrix, Illumina [20536605] (imputed) 125 mean corpuscular hemoglobin concentration http://www.ebi.ac.uk/efo/EFO_0004528 GCST90018965 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Mean corpuscular volume 350,473 European ancestry individuals, 129,832 East Asian ancestry individuals NA Affymetrix, Illumina [20535844] (imputed) 425 mean corpuscular volume http://www.ebi.ac.uk/efo/EFO_0004526 GCST90018966 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Monocyte count 349,856 European ancestry individuals, 95,119 East Asian ancestry individuals NA Affymetrix, Illumina [20531031] (imputed) 355 monocyte count http://www.ebi.ac.uk/efo/EFO_0005091 GCST90018967 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Neutrophil count 349,856 European ancestry individuals, 82,810 East Asian ancestry individuals NA Affymetrix, Illumina [20526770] (imputed) 343 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90018968 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Platelet count 350,474 European ancestry individuals, 148,623 East Asian ancestry individuals NA Affymetrix, Illumina [20538505] (imputed) 516 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90018969 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Pulse pressure 360,863 European ancestry individuals, 145,445 East Asian ancestry individuals NA Affymetrix, Illumina [20537391] (imputed) 333 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90018970 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Red blood cell count 350,475 European ancestry individuals, 153,512 East Asian ancestry individuals NA Affymetrix, Illumina [20538708] (imputed) 425 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90018971 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Systolic blood pressure 340,159 European ancestry individuals, 145,505 East Asian ancestry individuals NA Affymetrix, Illumina [20537302] (imputed) 300 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90018972 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Total bilirubin levels 342,829 European ancestry individuals, 124,341 East Asian ancestry individuals NA Affymetrix, Illumina [20535842] (imputed) 145 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90018973 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Total cholesterol levels 344,278 European ancestry individuals, 135,808 East Asian ancestry individuals NA Affymetrix, Illumina [20536134] (imputed) 183 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90018974 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Triglycerides 343,992 European ancestry individuals, 111,667 East Asian ancestry individuals NA Affymetrix, Illumina [20531459] (imputed) 258 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90018975 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum total protein levels 314,921 European ancestry individuals, 133,321 East Asian ancestry individuals NA Affymetrix, Illumina [20536782] (imputed) 297 total blood protein measurement http://www.ebi.ac.uk/efo/EFO_0004536 GCST90018976 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum uric acid levels 343,836 European ancestry individuals, 129,405 East Asian ancestry individuals NA Affymetrix, Illumina [20535231] (imputed) 279 uric acid measurement http://www.ebi.ac.uk/efo/EFO_0004761 GCST90018977 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. White blood cell count 350,470 European ancestry individuals, 154,355 East Asian ancestry individuals NA Affymetrix, Illumina [20538670] (imputed) 420 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90018978 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Serum creatinine levels 344,104 European ancestry individuals, 150,266 East Asian ancestry individuals NA Affymetrix, Illumina [20538295] (imputed) 427 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90018979 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (drugs for peptic ulcer and gastro-oesophageal reflux disease) 53,137 European ancestry cases, 79,230 European ancestry controls, 53,363 East Asian ancestry cases, 125,363 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 6 Peptic ulcer and gastro-oesophageal reflux disease (GORD) drug use measurement http://www.ebi.ac.uk/efo/EFO_0009923 GCST90018980 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (drugs used in diabetes) 15,272 European ancestry cases, 290,641 European ancestry controls, 30,515 East Asian ancestry cases, 148,211 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 122 Drugs used in diabetes use measurement http://www.ebi.ac.uk/efo/EFO_0009924 GCST90018981 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antithrombotic agents) 67,653 European ancestry cases, 85,986 European ancestry controls, 54,220 East Asian ancestry cases, 124,506 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 35 Antithrombotic agent use measurement http://www.ebi.ac.uk/efo/EFO_0009925 GCST90018982 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (vasodilators used in cardiac diseases) 5,546 European ancestry cases, 237,113 European ancestry controls, 17,050 East Asian ancestry cases, 161,676 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 24 Vasodilators used in cardiac diseases use measurement http://www.ebi.ac.uk/efo/EFO_0009926 GCST90018983 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (antihypertensives) 6,431 European ancestry cases, 145,949 European ancestry controls, 5,688 East Asian ancestry cases, 173,038 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 8 Antihypertensive use measurement http://www.ebi.ac.uk/efo/EFO_0009927 GCST90018984 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (diuretics) 34,453 European ancestry cases, 194,633 European ancestry controls, 22,356 East Asian ancestry cases, 156,370 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 87 Diuretic use measurement http://www.ebi.ac.uk/efo/EFO_0009928 GCST90018985 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (beta blocking agents) 31,700 European ancestry cases, 192,324 European ancestry controls, 20,367 East Asian ancestry cases, 158,359 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 72 Beta blocking agent use measurement http://www.ebi.ac.uk/efo/EFO_0009929 GCST90018986 Genome-wide genotyping array 2021-12-14 34594039 Sakaue S 2021-09-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34594039 A cross-population atlas of genetic associations for 220 human phenotypes. Medication use (calcium channel blockers) 31,904 European ancestry cases, 172,474 European ancestry controls, 49,327 East Asian ancestry cases, 129,399 East Asian ancestry controls NA Affymetrix, Illumina [15248280] (imputed) 113 Calcium channel blocker use measurement http://www.ebi.ac.uk/efo/EFO_0009930 GCST90018987 Genome-wide genotyping array 2022-09-30 36076102 Campbell M 2022-09-08 Surg Endosc www.ncbi.nlm.nih.gov/pubmed/36076102 Identification of 14 novel susceptibility loci for diaphragmatic hernia development and their biological and clinical implications: results from the UK Biobank. ICD10 K44: Diaphragmatic hernia 275,546 individuals 91,850 individuals NR [8568156] (imputed) 14 diaphragmatic hernia http://www.ebi.ac.uk/efo/EFO_0008561 GCST90140994 Genome-wide genotyping array 2022-10-12 36121873 Gilchrist JJ 2022-09-19 PLoS Pathog www.ncbi.nlm.nih.gov/pubmed/36121873 Genome-wide association study of leprosy in Malawi and Mali. Leprosy 284 Sub-Saharan African ancestry cases, 328 Sub-Saharan African ancestry controls NA Illumina [9519421] (imputed) 38 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST90129399 Genome-wide genotyping array 2022-10-12 36121873 Gilchrist JJ 2022-09-19 PLoS Pathog www.ncbi.nlm.nih.gov/pubmed/36121873 Genome-wide association study of leprosy in Malawi and Mali. Leprosy 208 Sub-Saharan African ancestry cases, 311 Sub-Saharan African ancestry controls NA Illumina [9448005] (imputed) 0 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST90129400 Genome-wide genotyping array 2022-10-12 36121873 Gilchrist JJ 2022-09-19 PLoS Pathog www.ncbi.nlm.nih.gov/pubmed/36121873 Genome-wide association study of leprosy in Malawi and Mali. Leprosy 492 Sub-Saharan African ancestry cases, 639 Sub-Saharan African ancestry controls NA Illumina [8578963] (imputed) 4 leprosy http://www.ebi.ac.uk/efo/EFO_0001054 GCST90129401 Genome-wide genotyping array 2023-02-24 36614910 Chung J 2022-12-23 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36614910 Genome-Wide Pleiotropy Study Identifies Association of PDGFB with Age-Related Macular Degeneration and COVID-19 Infection Outcomes. Age-related macular degeneration or COVID-19 critical illness (MTAG) 16,144 European ancestry AMD cases, 5,101 European ancestry COVID-19 critical illness cases, 1,401,064 European ancestry controls NA NR [NR] 53 age-related macular degeneration, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90250832 Genome-wide genotyping array 2023-02-24 36614910 Chung J 2022-12-23 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36614910 Genome-Wide Pleiotropy Study Identifies Association of PDGFB with Age-Related Macular Degeneration and COVID-19 Infection Outcomes. Age-related macular degeneration or COVID-19 hospitalization (MTAG) 16,144 European ancestry AMD cases, 9,986 European ancestry COVID-19 hospitalization cases, 1,895,495 European ancestry controls NA NR [NR] 53 age-related macular degeneration, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90250833 Genome-wide genotyping array 2023-02-24 36614910 Chung J 2022-12-23 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36614910 Genome-Wide Pleiotropy Study Identifies Association of PDGFB with Age-Related Macular Degeneration and COVID-19 Infection Outcomes. Age-related macular degeneration or COVID-19 infection (MTAG) 16,144 European ancestry AMD cases, 38,984 European ancestry COVID-19 infection cases, 1,662,607 European ancestry controls NA NR [NR] 53 age-related macular degeneration, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90250834 Genome-wide genotyping array 2023-02-24 36614910 Chung J 2022-12-23 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36614910 Genome-Wide Pleiotropy Study Identifies Association of PDGFB with Age-Related Macular Degeneration and COVID-19 Infection Outcomes. COVID-19 critical illness or age-related macular degeneration (MTAG) 5,101 European ancestry COVID-19 critical illness cases, 16,144 European ancestry AMD cases, 1,401,064 European ancestry controls NA NR [NR] 11 age-related macular degeneration, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90250835 Genome-wide genotyping array 2023-02-24 36614910 Chung J 2022-12-23 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36614910 Genome-Wide Pleiotropy Study Identifies Association of PDGFB with Age-Related Macular Degeneration and COVID-19 Infection Outcomes. COVID-19 hospitalization or age-related macular degeneration (MTAG) 9,986 European ancestry COVID-19 hospitalization cases, 16,144 European ancestry AMD cases, 1,895,495 European ancestry controls NA NR [NR] 7 age-related macular degeneration, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90250836 Genome-wide genotyping array 2023-02-24 36614910 Chung J 2022-12-23 J Clin Med www.ncbi.nlm.nih.gov/pubmed/36614910 Genome-Wide Pleiotropy Study Identifies Association of PDGFB with Age-Related Macular Degeneration and COVID-19 Infection Outcomes. COVID-19 infection or age-related macular degeneration (MTAG) 38,984 European ancestry COVID-19 infection cases, 16,144 European ancestry AMD cases, 1,662,607 European ancestry controls NA NR [NR] 11 age-related macular degeneration, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90250837 Genome-wide genotyping array 2022-09-28 35290122 Wu Y 2022-03-14 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/35290122 GWAS on birth year infant mortality rates provides evidence of recent natural selection. Birth year infant mortality rates 330,340 European ancestry individuals NA NR [6987228] (imputed) 2 Death in infancy http://purl.obolibrary.org/obo/HP_0001522 GCST90095047 Genome-wide genotyping array 2023-07-26 36752565 Esoh KK 2023-02-08 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36752565 Genome-wide association study identifies novel candidate malaria resistance genes in Cameroon. Malaria 1,103 Cameroonian ancestry individuals NA Illumina [NR] (imputed) 5 malaria http://www.ebi.ac.uk/efo/EFO_0001068 GCST90274860 Genome-wide genotyping array 2023-09-04 36738287 Li YJ 2023-02-04 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/36738287 Identification of novel genes for age-at-onset of Alzheimer's disease by combining quantitative and survival trait analyses. Alzheimer's disease (age of onset) 9,219 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 8 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST90281035 Genome-wide genotyping array 2023-09-04 36738287 Li YJ 2023-02-04 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/36738287 Identification of novel genes for age-at-onset of Alzheimer's disease by combining quantitative and survival trait analyses. Alzheimer's disease (age of onset) 9,219 European ancestry cases, 10,345 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 15 age of onset of Alzheimer disease http://purl.obolibrary.org/obo/OBA_2001000 GCST90281036 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA3 volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 7 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267919 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA4 volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 20 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267920 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA4 volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 17 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267921 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right fimbria volume 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 0 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST90267922 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal right GC-ML-DG volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 14 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267923 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal right GC-ML-DG volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 16 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267924 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal right HATA volume 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 3 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST90267925 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 20 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267926 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (fissure) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 9 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267927 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 20 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267928 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (tail) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 26 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267929 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume 65,791 European ancestry, East Asian ancestry individuals NA NR [5048682] (imputed) 48 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267930 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right molecular layer hippocampal volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 10 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267931 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right molecular layer hippocampal volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 11 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267932 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right parasubiculum volume 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 1 parasubiculum volume http://www.ebi.ac.uk/efo/EFO_0009405 GCST90267933 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right presubiculum volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 8 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267934 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right presubiculum volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 8 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267935 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right subiculum volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 19 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267936 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right subiculum volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 16 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267937 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA1 volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267938 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA1 volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267939 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA3 volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267940 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA3 volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267941 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA4 volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267942 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA4 volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 3 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267943 Genome-wide genotyping array 2023-11-13 37871108 Pasanen A 2023-10-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37871108 Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. Gestational duration 24,391 Finnish ancestry individuals NA Affymetrix, Illumina [15942625] (imputed) 0 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST90271752 Genome-wide genotyping array 2023-11-13 37871108 Pasanen A 2023-10-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37871108 Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. Spontaneous preterm birth 4,925 Finnish ancestry cases, 49,105 Finnish ancestry controls NA Affymetrix, Illumina [15955907] (imputed) 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90271753 Genome-wide genotyping array 2023-11-13 37871108 Pasanen A 2023-10-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37871108 Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. Gestational duration 774 Finnish ancestry individuals NA Illumina [8952530] (imputed) 0 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST90271754 Genome-wide genotyping array 2023-11-13 37871108 Pasanen A 2023-10-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37871108 Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. Spontaneous preterm birth 286 Finnish ancestry cases, 488 Finnish ancestry controls NA Illumina [8959678] (imputed) 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90271755 Genome-wide genotyping array 2023-11-13 37871108 Pasanen A 2023-10-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37871108 Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. Gestational duration 68,732 European ancestry individuals 8,643 European ancestry individuals Affymetrix, Illumina [10993596] (imputed) 15 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST90271756 Genome-wide genotyping array 2023-11-13 37871108 Pasanen A 2023-10-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37871108 Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci. Spontaneous preterm birth 8,542 European ancestry cases, 89,828 European ancestry controls 8,643 European ancestry individuals Affymetrix, Illumina [10978783] (imputed) 2 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90271757 Genome-wide genotyping array 2023-10-23 25629528 Ruggiero D 2015-01-28 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/25629528 Genetic variants modulating CRIPTO serum levels identified by genome-wide association study in Cilento isolates. Cripto levels (serum) 1,054 Cilento (founder/genetic isolate) individuals 535 Cilento (founder/genetic isolate) individuals Illumina [6222455] (imputed) 6 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90296099 Genome-wide genotyping array 2023-07-27 35368071 Pereira AC 2022-04-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35368071 Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID study. COVID-19 severity 2,453 European ancestry hospitalised cases, 956 European ancestry non-hospitalised controls, up to 757 hospitalised cases, up to 501 non-hospitalised controls, 244 African ancestry hospitalised cases, 201 African ancestry non-hospitalised controls, 1 Native Brazilian ancestry hospitalised case, 4 Native Brazilian ancestry non-hospitalised controls, 39 Asian ancestry hospitalised cases, 30 Asian ancestry non-hospitalised controls NA Affymetrix [11395074] (imputed) 5 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90239839 Genome-wide genotyping array 2023-07-27 35368071 Pereira AC 2022-04-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35368071 Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID study. COVID-19 severity 2,453 European ancestry hospitalised cases, 956 European ancestry non-hospitalised controls, up to 15,237 hospitalised cases, up to 73,692 non-hospitalised controls, 244 African ancestry hospitalised cases, 201 African ancestry non-hospitalised controls, 1 Native Brazilian ancestry hospitalised case, 4 Native Brazilian ancestry non-hospitalised controls, 39 Asian ancestry hospitalised cases, 30 Asian ancestry non-hospitalised controls NA Affymetrix [11395074] (imputed) 8 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90274861 Genome-wide genotyping array 2023-07-27 35368071 Pereira AC 2022-04-02 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35368071 Genetic risk factors and COVID-19 severity in Brazil: results from BRACOVID study. COVID-19 severity 2,453 European ancestry hospitalised cases, 956 European ancestry non-hospitalised controls, up to 25,031 hospitalised cases, up to 2,062,030 non-hospitalised or general population controls, 244 African ancestry hospitalised cases, 201 African ancestry non-hospitalised controls, 1 Native Brazilian ancestry hospitalised case, 4 Native Brazilian ancestry non-hospitalised controls, 39 Asian ancestry hospitalised cases, 30 Asian ancestry non-hospitalised controls NA Affymetrix [11395074] (imputed) 28 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90274862 Genome-wide genotyping array 2023-11-13 37877466 Pujol Gualdo N 2023-10-24 Hum Reprod www.ncbi.nlm.nih.gov/pubmed/37877466 Genome-wide association study meta-analysis supports association between MUC1 and ectopic pregnancy. Ectopic pregnancy 7,070 European ancestry cases, 248,810 European ancestry controls NA NR [18241848] (imputed) 2 Ectopic pregnancy http://purl.obolibrary.org/obo/HP_0031456 GCST90272883 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K35: Acute appendicitis 696 Chinese ancestry cases, 75,314 Chinese ancestry controls NA Affymetrix [8845246] (imputed) 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90246137 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K37: Unspecified appendicitis 268 Chinese ancestry cases, 75,631 Chinese ancestry controls NA Affymetrix [7832200] (imputed) 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90246138 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K40: Inguinal hernia 251 Chinese ancestry cases, 75,661 Chinese ancestry controls NA Affymetrix [7753348] (imputed) 0 Inguinal hernia http://purl.obolibrary.org/obo/HP_0000023 GCST90246139 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K52: Other and unspecified noninfective gastroenteritis and colitis 145 Chinese ancestry cases, 75,758 Chinese ancestry controls NA Affymetrix [7058025] (imputed) 0 gastroenteritis http://www.ebi.ac.uk/efo/EFO_1001463 GCST90246140 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K56: Paralytic ileus and intestinal obstruction without hernia 666 Chinese ancestry cases, 75,391 Chinese ancestry controls NA Affymetrix [8821031] (imputed) 0 Gastrointestinal obstruction http://purl.obolibrary.org/obo/HP_0004796 GCST90246141 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K59: Other functional intestinal disorders 115 Chinese ancestry cases, 75,767 Chinese ancestry controls NA Affymetrix [6733547] (imputed) 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90246142 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K60: Fissure and fistula of anal and rectal regions 191 Chinese ancestry cases, 75,688 Chinese ancestry controls NA Affymetrix [7417820] (imputed) 1 Anal fissure http://purl.obolibrary.org/obo/HP_0012390 GCST90246143 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K61: Abscess of anal and rectal regions 157 Chinese ancestry cases, 75,735 Chinese ancestry controls NA Affymetrix [7161757] (imputed) 0 Rectal abscess http://purl.obolibrary.org/obo/HP_0005224 GCST90246144 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K62: Other diseases of anus and rectum 289 Chinese ancestry cases, 75,621 Chinese ancestry controls NA Affymetrix [7925099] (imputed) 0 anus disease, rectal disease http://www.ebi.ac.uk/efo/EFO_0009660, http://www.ebi.ac.uk/efo/EFO_0009685 GCST90246145 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K63: Other diseases of intestine 558 Chinese ancestry cases, 75,390 Chinese ancestry controls NA Affymetrix [8689359] (imputed) 0 intestinal disease http://www.ebi.ac.uk/efo/EFO_0009431 GCST90246146 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K64: Hemorrhoids and perianal venous thrombosis 1,386 Chinese ancestry cases, 74,718 Chinese ancestry controls NA Affymetrix [8984321] (imputed) 1 hemorrhoid http://www.ebi.ac.uk/efo/EFO_0009552 GCST90246147 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K74: Fibrosis and cirrhosis of liver 503 Chinese ancestry cases, 75,490 Chinese ancestry controls NA Affymetrix [8583249] (imputed) 1 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90246148 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K75: Other inflammatory liver diseases 172 Chinese ancestry cases, 75,717 Chinese ancestry controls NA Affymetrix [7280467] (imputed) 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90246149 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K76: Other diseases of liver 523 Chinese ancestry cases, 75,489 Chinese ancestry controls NA Affymetrix [8626509] (imputed) 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90246150 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K80: Cholelithiasis 2,230 Chinese ancestry cases, 74,222 Chinese ancestry controls NA Affymetrix [8992920] (imputed) 0 cholelithiasis http://www.ebi.ac.uk/efo/EFO_0004799 GCST90246151 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K81: Cholecystitis 1,419 Chinese ancestry cases, 74,871 Chinese ancestry controls NA Affymetrix [8985246] (imputed) 1 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90246152 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K82: Other diseases of gallbladder 140 Chinese ancestry cases, 75,743 Chinese ancestry controls NA Affymetrix [7010164] (imputed) 0 gallbladder disease http://www.ebi.ac.uk/efo/EFO_0003832 GCST90246153 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K83: Other diseases of biliary tract 256 Chinese ancestry cases, 75,670 Chinese ancestry controls NA Affymetrix [7777145] (imputed) 0 biliary tract disease http://www.ebi.ac.uk/efo/EFO_0009534 GCST90246154 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K85: Acute pancreatitis 313 Chinese ancestry cases, 75,608 Chinese ancestry controls NA Affymetrix [8018243] (imputed) 0 pancreatitis http://www.ebi.ac.uk/efo/EFO_0000278 GCST90246155 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K86: Other diseases of pancreas 180 Chinese ancestry cases, 75,719 Chinese ancestry controls NA Affymetrix [7341267] (imputed) 0 pancreas disease http://www.ebi.ac.uk/efo/EFO_0009605 GCST90246156 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K92: Other diseases of digestive system 908 Chinese ancestry cases, 75,242 Chinese ancestry controls NA Affymetrix [8939283] (imputed) 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90246157 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 L02: Cutaneous abscess, furuncle and carbuncle 103 Chinese ancestry cases, 75,774 Chinese ancestry controls NA Affymetrix [6571195] (imputed) 0 Cutaneous abscess http://purl.obolibrary.org/obo/HP_0031292 GCST90246158 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Other dermatitis (Union L30) 183 Chinese ancestry cases, 75,706 Chinese ancestry controls NA Affymetrix [7362417] (imputed) 0 contact dermatitis http://www.ebi.ac.uk/efo/EFO_0005319 GCST90246159 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Decubitus ulcer (Union L89) 160 Chinese ancestry cases, 75,761 Chinese ancestry controls NA Affymetrix [7186589] (imputed) 0 decubitus ulcer http://www.ebi.ac.uk/efo/EFO_0007067 GCST90246160 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M06: Other rheumatoid arthritis 443 Chinese ancestry cases, 75,545 Chinese ancestry controls NA Affymetrix [8429467] (imputed) 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90246161 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M10: Gout 269 Chinese ancestry cases, 75,687 Chinese ancestry controls NA Affymetrix [7836912] (imputed) 1 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90246162 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M17: Osteoarthritis of knee 339 Chinese ancestry cases, 75,608 Chinese ancestry controls NA Affymetrix [8111916] (imputed) 0 osteoarthritis, knee http://www.ebi.ac.uk/efo/EFO_0004616 GCST90246163 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Other arthrosis (Union M19) 1,488 Chinese ancestry cases, 74,783 Chinese ancestry controls NA Affymetrix [8986528] (imputed) 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90246164 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M25: Other joint disorder, not elsewhere classified 130 Chinese ancestry cases, 75,753 Chinese ancestry controls NA Affymetrix [6908084] (imputed) 0 joint disease http://www.ebi.ac.uk/efo/EFO_1000999 GCST90246165 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M47: Spondylosis 2,607 Chinese ancestry cases, 74,037 Chinese ancestry controls NA Affymetrix [8994324] (imputed) 2 spondylosis http://purl.obolibrary.org/obo/MONDO_0002253 GCST90246166 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M48: Other spondylopathies 455 Chinese ancestry cases, 75,501 Chinese ancestry controls NA Affymetrix [8462062] (imputed) 0 bone disease http://www.ebi.ac.uk/efo/EFO_0004260 GCST90246167 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M50: Cervical disc disorders 446 Chinese ancestry cases, 75,501 Chinese ancestry controls NA Affymetrix [8437536] (imputed) 0 cervical disc degenerative disorder http://www.ebi.ac.uk/efo/EFO_0009537 GCST90246168 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Other intervertebral disk disorders (Union M51) 3,039 Chinese ancestry cases, 73,642 Chinese ancestry controls NA Affymetrix [8994829] (imputed) 0 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST90246169 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M54: Dorsalgia 309 Chinese ancestry cases, 75,633 Chinese ancestry controls NA Affymetrix [8002966] (imputed) 0 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90246170 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M75: Shoulder lesions 100 Chinese ancestry cases, 75,781 Chinese ancestry controls NA Affymetrix [6526716] (imputed) 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90246171 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M79: Other and unspecified soft tissue disorders, not elsewhere classified 118 Chinese ancestry cases, 75,768 Chinese ancestry controls NA Affymetrix [6771116] (imputed) 0 soft tissue disease http://www.ebi.ac.uk/efo/EFO_0009470 GCST90246172 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M80: Osteoporosis with current pathological fracture 129 Chinese ancestry cases, 75,756 Chinese ancestry controls NA Affymetrix [6897083] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90246173 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M81: Osteoporosis without current pathological fracture 390 Chinese ancestry cases, 75,598 Chinese ancestry controls NA Affymetrix [8278801] (imputed) 0 osteoporosis http://www.ebi.ac.uk/efo/EFO_0003882 GCST90246174 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 M87: Osteonecrosis 132 Chinese ancestry cases, 75,751 Chinese ancestry controls NA Affymetrix [6929328] (imputed) 0 osteonecrosis http://www.ebi.ac.uk/efo/EFO_0004259 GCST90246175 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N03: Chronic nephritic syndrome 230 Chinese ancestry cases, 75,690 Chinese ancestry controls NA Affymetrix [7647991] (imputed) 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90246176 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Nephrotic syndrome (Union N04) 113 Chinese ancestry cases, 75,767 Chinese ancestry controls NA Affymetrix [6707993] (imputed) 0 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90246177 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Acute tubulo-interstitial nephritis (Union N10) 214 Chinese ancestry cases, 75,702 Chinese ancestry controls NA Affymetrix [7557586] (imputed) 0 Acute tubulointerstitial nephritis http://purl.obolibrary.org/obo/HP_0004729 GCST90246178 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N13: Obstructive and reflux uropathy 204 Chinese ancestry cases, 75,695 Chinese ancestry controls NA Affymetrix [7499637] (imputed) 0 urinary tract obstruction http://www.ebi.ac.uk/efo/EFO_0009571 GCST90246179 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N18: Chronic kidney disease 489 Chinese ancestry cases, 75,531 Chinese ancestry controls NA Affymetrix [8548668] (imputed) 0 chronic kidney disease http://www.ebi.ac.uk/efo/EFO_0003884 GCST90246180 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N19: Unspecified kidney failure 621 Chinese ancestry cases, 75,465 Chinese ancestry controls NA Affymetrix [8775394] (imputed) 0 kidney failure http://www.ebi.ac.uk/efo/EFO_1002048 GCST90246181 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N20: Calculus of kidney and ureter 2,047 Chinese ancestry cases, 74,398 Chinese ancestry controls NA Affymetrix [8992019] (imputed) 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90246182 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N21: Calculus of lower urinary tract 131 Chinese ancestry cases, 75,766 Chinese ancestry controls NA Affymetrix [6918727] (imputed) 0 ureterolithiasis http://www.ebi.ac.uk/efo/EFO_1001228 GCST90246183 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N23: Unspecified renal colic 289 Chinese ancestry cases, 75,668 Chinese ancestry controls NA Affymetrix [7925077] (imputed) 0 renal colic http://www.ebi.ac.uk/efo/EFO_1001412 GCST90246184 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N28: Other disorders of kidney and ureter, not elsewhere classified 231 Chinese ancestry cases, 75,691 Chinese ancestry controls NA Affymetrix [7653222] (imputed) 0 kidney disease http://www.ebi.ac.uk/efo/EFO_0003086 GCST90246185 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N30: Cystitis 137 Chinese ancestry cases, 75,760 Chinese ancestry controls NA Affymetrix [6980991] (imputed) 0 cystitis http://www.ebi.ac.uk/efo/EFO_1000025 GCST90246186 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N39: Other disorders of urinary system 908 Chinese ancestry cases, 75,222 Chinese ancestry controls NA Affymetrix [8939180] (imputed) 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90246187 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Hyperplasia of prostate (Union N40) 903 Chinese ancestry cases, 29,976 Chinese ancestry controls NA Affymetrix [8932998] (imputed) 1 benign prostatic hyperplasia http://www.ebi.ac.uk/efo/EFO_0000284 GCST90246188 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N41: Inflammatory diseases of prostate 169 Chinese ancestry cases, 30,424 Chinese ancestry controls NA Affymetrix [7252559] (imputed) 1 prostatitis http://www.ebi.ac.uk/efo/EFO_0003830 GCST90246189 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N63: Unspecified lump in breast 170 Chinese ancestry cases, 45,165 Chinese ancestry controls NA Affymetrix [7263598] (imputed) 1 breast cyst http://www.ebi.ac.uk/efo/EFO_1000848 GCST90246190 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N72: Inflammatory disease of cervix uteri 194 Chinese ancestry cases, 45,163 Chinese ancestry controls NA Affymetrix [7435537] (imputed) 0 Cervicitis http://purl.obolibrary.org/obo/HP_0030160 GCST90246191 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N73: Other female pelvic inflammatory diseases 338 Chinese ancestry cases, 45,057 Chinese ancestry controls NA Affymetrix [8105388] (imputed) 0 Pelvic Inflammatory Disease http://www.ebi.ac.uk/efo/EFO_1001388 GCST90246192 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N80: Endometriosis 188 Chinese ancestry cases, 45,154 Chinese ancestry controls NA Affymetrix [7395528] (imputed) 0 endometriosis http://www.ebi.ac.uk/efo/EFO_0001065 GCST90246193 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N81: Female genital prolapse 122 Chinese ancestry cases, 45,221 Chinese ancestry controls NA Affymetrix [6816918] (imputed) 0 uterine prolapse http://www.ebi.ac.uk/efo/EFO_1001864 GCST90246194 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N83: Noninflammatory disorders of ovary, fallopian tube and broad ligament 177 Chinese ancestry cases, 45,183 Chinese ancestry controls NA Affymetrix [7317797] (imputed) 0 female reproductive system disease http://www.ebi.ac.uk/efo/EFO_0009549 GCST90246195 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N84: Polyp of female genital tract 188 Chinese ancestry cases, 45,171 Chinese ancestry controls NA Affymetrix [7395563] (imputed) 0 uterine polyp http://www.ebi.ac.uk/efo/EFO_0009484 GCST90246196 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 N93: Other abnormal uterine and vaginal bleeding 133 Chinese ancestry cases, 45,219 Chinese ancestry controls NA Affymetrix [6937949] (imputed) 0 Metrorrhagia http://purl.obolibrary.org/obo/HP_0100608 GCST90246197 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 O80: Encounter for full-term uncomplicated delivery 317 Chinese ancestry cases, 75,647 Chinese ancestry controls NA Affymetrix [8033117] (imputed) 1 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90246198 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R00: Abnormalities of heart beat 277 Chinese ancestry cases, 75,681 Chinese ancestry controls NA Affymetrix [7873062] (imputed) 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90246199 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R04: Hemorrhage from respiratory passages 236 Chinese ancestry cases, 75,693 Chinese ancestry controls NA Affymetrix [7679052] (imputed) 0 hemorrhage http://purl.obolibrary.org/obo/MP_0001914 GCST90246200 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R05: Cough 101 Chinese ancestry cases, 75,783 Chinese ancestry controls NA Affymetrix [6541853] (imputed) 0 Cough http://purl.obolibrary.org/obo/HP_0012735 GCST90246201 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R07: Pain in throat and chest 193 Chinese ancestry cases, 75,699 Chinese ancestry controls NA Affymetrix [7431168] (imputed) 0 Chest pain http://purl.obolibrary.org/obo/HP_0100749 GCST90246202 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R09: Other symptoms and signs involving the circulatory and respiratory system 117 Chinese ancestry cases, 75,776 Chinese ancestry controls NA Affymetrix [6758652] (imputed) 0 respiratory symptom measurement http://www.ebi.ac.uk/efo/EFO_0007939 GCST90246203 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R10: Abdominal and pelvic pain 631 Chinese ancestry cases, 75,415 Chinese ancestry controls NA Affymetrix [8786466] (imputed) 0 Abdominal pain http://purl.obolibrary.org/obo/HP_0002027 GCST90246204 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R22: Localized swelling, mass and lump of skin and subcutaneous tissue 171 Chinese ancestry cases, 75,715 Chinese ancestry controls NA Affymetrix [7272751] (imputed) 0 primary lymphedema http://purl.obolibrary.org/obo/MONDO_0019175 GCST90246205 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R33: Retention of urine 176 Chinese ancestry cases, 75,748 Chinese ancestry controls NA Affymetrix [7311585] (imputed) 0 Urinary retention http://purl.obolibrary.org/obo/HP_0000016 GCST90246206 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R42: Dizziness and giddiness 1,018 Chinese ancestry cases, 75,133 Chinese ancestry controls NA Affymetrix [8959523] (imputed) 0 dizziness http://www.ebi.ac.uk/efo/EFO_0009847 GCST90246207 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R50: Fever of other and unknown origin 319 Chinese ancestry cases, 75,609 Chinese ancestry controls NA Affymetrix [8040609] (imputed) 0 fever of unknown origin http://www.ebi.ac.uk/efo/EFO_0003952 GCST90246208 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R51: Headache 507 Chinese ancestry cases, 75,487 Chinese ancestry controls NA Affymetrix [8592500] (imputed) 0 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90246209 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R55: Syncope and collapse 113 Chinese ancestry cases, 75,780 Chinese ancestry controls NA Affymetrix [6707989] (imputed) 0 Syncope http://purl.obolibrary.org/obo/HP_0001279 GCST90246210 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R57: Shock, not elsewhere classified 227 Chinese ancestry cases, 75,712 Chinese ancestry controls NA Affymetrix [7632243] (imputed) 0 Shock http://purl.obolibrary.org/obo/HP_0031273 GCST90246211 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Unknown and unspecified causes of morbidity (Union R69) 5,131 Chinese ancestry cases, 72,426 Chinese ancestry controls NA Affymetrix [8996331] (imputed) 0 disease http://www.ebi.ac.uk/efo/EFO_0000408 GCST90246212 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R93: Abnormal findings on diagnostic imaging of other body structures 107 Chinese ancestry cases, 75,766 Chinese ancestry controls NA Affymetrix [6627454] (imputed) 0 abnormal result of diagnostic imaging http://www.ebi.ac.uk/efo/EFO_0009827 GCST90246213 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 R94: Abnormal results of function studies 169 Chinese ancestry cases, 75,730 Chinese ancestry controls NA Affymetrix [7257497] (imputed) 0 abnormal result of function studies http://www.ebi.ac.uk/efo/EFO_0009628 GCST90246214 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD-10 R96: Other sudden death, cause unknown 118 Chinese ancestry cases, 75,786 Chinese ancestry controls NA Affymetrix [6771012] (imputed) 0 Sudden death http://purl.obolibrary.org/obo/HP_0001699 GCST90246215 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Other ill-defined and unspecified causes of mortality (Union R99) 176 Chinese ancestry cases, 75,723 Chinese ancestry controls NA Affymetrix [7311562] (imputed) 0 mortality http://www.ebi.ac.uk/efo/EFO_0004352 GCST90246216 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S00: Superficial injury of head 101 Chinese ancestry cases, 75,788 Chinese ancestry controls NA Affymetrix [6541897] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90246217 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S06: Intracranial injury 628 Chinese ancestry cases, 75,463 Chinese ancestry controls NA Affymetrix [8783167] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90246218 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S09: Other and unspecified injuries of head 162 Chinese ancestry cases, 75,732 Chinese ancestry controls NA Affymetrix [7202334] (imputed) 0 head injury http://www.ebi.ac.uk/efo/EFO_0009505 GCST90246219 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S22: Fracture of rib(s), sternum and thoracic spine 449 Chinese ancestry cases, 75,545 Chinese ancestry controls NA Affymetrix [8445448] (imputed) 1 rib fracture http://www.ebi.ac.uk/efo/EFO_0009620 GCST90246220 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S32: Fracture of lumbar spine and pelvis 470 Chinese ancestry cases, 75,505 Chinese ancestry controls NA Affymetrix [8500246] (imputed) 0 spinal fracture http://www.ebi.ac.uk/efo/EFO_0003902 GCST90246221 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S42: Fracture of shoulder and upper arm 403 Chinese ancestry cases, 75,554 Chinese ancestry controls NA Affymetrix [8317802] (imputed) 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90246222 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S52: Fracture of forearm 382 Chinese ancestry cases, 75,551 Chinese ancestry controls NA Affymetrix [8255022] (imputed) 0 upper extremity fracture http://www.ebi.ac.uk/efo/EFO_0009514 GCST90246223 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S72: Fracture of femur 777 Chinese ancestry cases, 75,336 Chinese ancestry controls NA Affymetrix [8894143] (imputed) 0 femur fracture http://www.ebi.ac.uk/efo/EFO_0008553 GCST90246224 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 S82: Fracture of lower leg, including ankle 596 Chinese ancestry cases, 75,392 Chinese ancestry controls NA Affymetrix [8744985] (imputed) 0 lower extremity fracture http://www.ebi.ac.uk/efo/EFO_0009512 GCST90246225 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 T14: Injury of unspecified body region 903 Chinese ancestry cases, 75,223 Chinese ancestry controls NA Affymetrix [8938058] (imputed) 0 injury http://www.ebi.ac.uk/efo/EFO_0000546 GCST90246226 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 Z04: Encounter for examination and observation for other reasons 799 Chinese ancestry cases, 75,297 Chinese ancestry controls NA Affymetrix [8903933] (imputed) 0 encounter with health service http://www.ebi.ac.uk/efo/EFO_0009786 GCST90246227 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 Z47: Orthopedic aftercare 103 Chinese ancestry cases, 75,761 Chinese ancestry controls NA Affymetrix [6571199] (imputed) 0 planned process http://www.ebi.ac.uk/efo/EFO_0004542 GCST90246228 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 Z96: Presence of other functional implants 567 Chinese ancestry cases, 75,441 Chinese ancestry controls NA Affymetrix [8703398] (imputed) 1 medical procedure http://www.ebi.ac.uk/efo/EFO_0002571 GCST90246229 Genome-wide genotyping array 2023-11-30 37828025 Hartmann S 2023-10-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37828025 ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon. Raynauds phenomenon disease 5,147 European ancestry cases, 439,294 European ancestry controls 401 South Asian ancestry cases, 40,131 South Asian ancestry controls Affymetrix [15519420] (imputed) 3 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90271713 Genome-wide genotyping array 2023-11-30 37828025 Hartmann S 2023-10-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37828025 ADRA2A and IRX1 are putative risk genes for Raynaud's phenomenon. Primary Raynaud’s phenomenon 3,505 European ancestry cases, 439,294 European ancestry controls NA Affymetrix [15519343] (imputed) 2 Raynaud disease http://www.ebi.ac.uk/efo/EFO_1001145 GCST90271714 Genome-wide genotyping array 2023-11-15 37236419 Zai CC 2023-05-24 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/37236419 A genome-wide association study of antidepressant-induced mania. Antidepressant-induced mania 287 European ancestry cases, 527 European ancestry controls NA Illumina [NR] (imputed) 1 bipolar disorder, antidepressant-induced side effect http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0006320 GCST90297548 Genome-wide genotyping array 2023-11-14 37919453 Nethander M 2023-11-02 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37919453 An atlas of genetic determinants of forearm fracture. Fracture of forearm 50,471 European ancestry cases, 969,623 European ancestry controls 49,555 cases, 620,360 controls Affymetrix, Illumina [8383044] (imputed) 57 bone fracture http://www.ebi.ac.uk/efo/EFO_0003931 GCST90281273 Genome-wide genotyping array 2023-09-05 37612283 Ito S 2023-08-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37612283 Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects. Prostate cancer 8,645 Japanese ancestry cases, 89,536 Japanese ancestry controls NA Illumina [9871525] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90269956 Genome-wide genotyping array 2023-09-05 37612283 Ito S 2023-08-23 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37612283 Androgen receptor binding sites enabling genetic prediction of mortality due to prostate cancer in cancer-free subjects. Prostate cancer 8,645 Japanese ancestry cases, 89,536 Japanese ancestry controls, 85,554 European ancestry cases, 91,972 European ancestry controls, 10,368 African ancestry cases, 10,986 African ancestry controls, 2,714 Hispanic cases, 5,239 Hispanic controls NA Affymetrix, Illumina [6873681] (imputed) 9 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90269957 Genome-wide genotyping array 2023-11-02 37859345 Sarsani V 2023-10-18 HGG Adv www.ncbi.nlm.nih.gov/pubmed/37859345 A Cross-ancestry genome-wide meta-analysis, fine-mapping, and gene prioritization approach to characterize the genetic architecture of adiponectin. Adiponectin levels 38,609 European ancestry individuals, 7,825 East Asian ancestry individuals 35,559 Icelandic ancestry individuals NR [2194781] (imputed) 21 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90293085 Genome-wide genotyping array 2023-11-02 37859345 Sarsani V 2023-10-18 HGG Adv www.ncbi.nlm.nih.gov/pubmed/37859345 A Cross-ancestry genome-wide meta-analysis, fine-mapping, and gene prioritization approach to characterize the genetic architecture of adiponectin. Adiponectin levels 38,609 European ancestry individuals NA NR [2498292] (imputed) 19 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90293086 Genome-wide genotyping array 2023-09-06 36446896 Mize TJ 2022-11-29 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36446896 Examination of a novel expression-based gene-SNP annotation strategy to identify tissue-specific contributions to heritability in multiple traits. Inflammatory bowel disease 4,859 European ancestry cases, 330,594 European ancestry controls NA NR [1124698] (imputed) 0 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90225550 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Migraine or 2-hr glucose levels 102,084 European ancestry migraine cases, 771,257 European ancestry controls without migraine, 64,469 European ancestry individuals with 2hr glucose NA NR [NR] 4 migraine disorder, glucose measurement http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0004468 GCST90281112 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Migraine or fasting glucose levels 102,084 European ancestry migraine cases, 771,257 European ancestry controls without migraine, 208,438 European ancestry individuals with fasting glucose NA NR [NR] 7 migraine disorder, fasting blood glucose measurement http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0004465 GCST90281113 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Migraine or fasting insulin levels 102,084 European ancestry migraine cases, 771,257 European ancestry controls without migraine, 151,903 European ancestry individuals with fasting insulin NA NR [NR] 5 migraine disorder, fasting blood insulin measurement http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0004466 GCST90281114 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Migraine or glucose levels 102,084 European ancestry migraine cases, 771,257 European ancestry controls without migraine, 366,759 European ancestry indviduals with glucose NA NR [NR] 19 migraine disorder, glucose measurement http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0004468 GCST90281115 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Migraine or HOMA-B 102,084 European ancestry migraine cases, 771,257 European ancestry controls without migraine, 36,466 European ancestry indviduals with HOMA-B NA NR [NR] 2 migraine disorder, HOMA-B http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0004469 GCST90281116 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Migraine or fasting pro-insulin levels 102,084 European ancestry migraine cases, 771,257 European ancestry controls without migraine, 10,701 European ancestry indviduals with HOMA-B NA NR [NR] 4 migraine disorder, fasting blood insulin measurement http://purl.obolibrary.org/obo/MONDO_0005277, http://www.ebi.ac.uk/efo/EFO_0004466 GCST90281117 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Migraine or type 1 diabetes 102,084 European ancestry migraine cases, 771,257 European ancestry controls without migraine, 3,250 European ancestry type 1 diabetes cases, 396,181 European ancestry controls without type 1 diabetes NA NR [NR] 3 migraine disorder, type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005277, http://purl.obolibrary.org/obo/MONDO_0005147 GCST90281118 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Headache or fasting glucose levels 84,036 European ancestry headache cases, 335,552 European ancestry controls without headache, 208,438 European ancestry individuals with fasting glucose NA NR [NR] 5 Headache, fasting blood glucose measurement http://purl.obolibrary.org/obo/HP_0002315, http://www.ebi.ac.uk/efo/EFO_0004465 GCST90281119 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Headache or fasting insulin levels 84,036 European ancestry headache cases, 335,552 European ancestry controls without headache, 151,903 European ancestry individuals with fasting insulin NA NR [NR] 4 Headache, fasting blood insulin measurement http://purl.obolibrary.org/obo/HP_0002315, http://www.ebi.ac.uk/efo/EFO_0004466 GCST90281120 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Headache or glucose levels 84,036 European ancestry headache cases, 335,552 European ancestry controls without headache, 366,759 European ancestry indviduals with glucose NA NR [NR] 9 Headache, glucose measurement http://purl.obolibrary.org/obo/HP_0002315, http://www.ebi.ac.uk/efo/EFO_0004468 GCST90281121 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Headache or HbA1c levels 84,036 European ancestry headache cases, 335,552 European ancestry controls without headache, 400,837 European ancestry indviduals with HbA1c NA NR [NR] 14 Headache, HbA1c measurement http://purl.obolibrary.org/obo/HP_0002315, http://www.ebi.ac.uk/efo/EFO_0004541 GCST90281122 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Headache or HOMA-B 84,036 European ancestry headache cases, 335,552 European ancestry controls without headache, 36,466 European ancestry indviduals with HOMA-B NA NR [NR] 4 Headache, HOMA-B http://purl.obolibrary.org/obo/HP_0002315, http://www.ebi.ac.uk/efo/EFO_0004469 GCST90281123 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Headache or HOMA-IR 84,036 European ancestry headache cases, 335,552 European ancestry controls without headache, 37,037 European ancestry indviduals with HOMA-IR NA NR [NR] 3 Headache, HOMA-IR http://purl.obolibrary.org/obo/HP_0002315, http://www.ebi.ac.uk/efo/EFO_0004501 GCST90281124 Genome-wide genotyping array 2023-09-06 36808568 Islam MR 2023-02-20 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36808568 Cross-trait analyses identify shared genetics between migraine, headache, and glycemic traits, and a causal relationship with fasting proinsulin. Headache or type 1 diabetes 84,036 European ancestry headache cases, 335,552 European ancestry controls without headache, 3,250 European ancestry type 1 diabetes cases, 396,181 European ancestry controls without type 1 diabetes NA NR [NR] 1 Headache, type 1 diabetes mellitus http://purl.obolibrary.org/obo/HP_0002315, http://purl.obolibrary.org/obo/MONDO_0005147 GCST90281125 Genome-wide genotyping array 2023-09-21 37669986 Kamiza AB 2023-09-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37669986 Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. Total cholesterol levels 125,000 African ancestry individuals NA Illumina [33765292] (imputed) 91 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90278113 Genome-wide genotyping array 2023-09-21 37669986 Kamiza AB 2023-09-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37669986 Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. Triglyceride levels 125,000 African ancestry individuals NA Illumina [33711617] (imputed) 48 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90278112 Genome-wide genotyping array 2023-09-21 37669986 Kamiza AB 2023-09-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37669986 Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. Low density lipoprotein cholesterol levels 125,000 African ancestry individuals NA Illumina [33765313] (imputed) 68 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90278111 Genome-wide genotyping array 2023-09-21 37669986 Kamiza AB 2023-09-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37669986 Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. High density lipoprotein cholesterol levels 125,000 African ancestry individuals NA Illumina [33621987] (imputed) 63 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90278110 Genome-wide genotyping array 2023-09-21 37669986 Kamiza AB 2023-09-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37669986 Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. High-density lipoprotein levels (MTAG) 125,000 African ancestry individuals (MTAG boosted by total cholesterol and triglyceride samples) NA Illumina [NR] (imputed) 84 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90292527 Genome-wide genotyping array 2023-09-21 37669986 Kamiza AB 2023-09-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37669986 Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. Triglyceride levels (MTAG) 125,000 African ancestry individuals (MTAG boosted by total cholesterol and high-density lipoprotein samples) NA Illumina [NR] (imputed) 62 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90292528 Genome-wide genotyping array 2023-09-21 37669986 Kamiza AB 2023-09-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37669986 Multi-trait discovery and fine-mapping of lipid loci in 125,000 individuals of African ancestry. Total cholesterol levels (MTAG) 125,000 African ancestry individuals (MTAG boosted by high-density lipoprotein and triglyceride samples) NA Illumina [NR] (imputed) 110 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90292529 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. uPA levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90244847 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CCL20 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CCL20 measurement http://www.ebi.ac.uk/efo/EFO_0010766 GCST90244822 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CCL4 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CCL4 measurement http://www.ebi.ac.uk/efo/EFO_0004751 GCST90244823 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CD40 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CD40 measurement http://www.ebi.ac.uk/efo/EFO_0010586 GCST90244824 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CD5 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CD5 measurement http://www.ebi.ac.uk/efo/EFO_0010773 GCST90244825 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CD6 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CD6 measurement http://www.ebi.ac.uk/efo/EFO_0010774 GCST90244826 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CSF1 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 colony stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010775 GCST90244827 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CXCL10 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CXCL10 measurement http://www.ebi.ac.uk/efo/EFO_0010778 GCST90244828 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CXCL1 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CXCL1 measurement http://www.ebi.ac.uk/efo/EFO_0010777 GCST90244829 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CXCL5 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CXCL5 measurement http://www.ebi.ac.uk/efo/EFO_0009422 GCST90244830 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. CXCL9 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CXCL9 measurement http://www.ebi.ac.uk/efo/EFO_0010780 GCST90244831 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. EN-RAGE levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90244832 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. Flt3L levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90244833 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. Interferon gamma levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90244834 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. Interleukin-1 alpha levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 obsolete_interleukin-1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0802653 GCST90244835 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. IL12B levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 obsolete_interleukin-12 subunit B measurement http://www.ebi.ac.uk/efo/EFO_0010787 GCST90244836 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. LAP TGFbeta1 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 transforming growth factor-beta measurement http://www.ebi.ac.uk/efo/EFO_0010799 GCST90244837 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. LIF levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 leukemia inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0801764 GCST90244838 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. MCP1 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 CCL2 measurement http://www.ebi.ac.uk/efo/EFO_0004749 GCST90244839 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. MCP2 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 monocyte chemotactic protein-2 measurement http://www.ebi.ac.uk/efo/EFO_0010789 GCST90244840 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. MCP3 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 monocyte chemotactic protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008235 GCST90244841 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. MMP-1 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90244842 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. OSM levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90244843 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. TGF alpha levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 transforming growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0010798 GCST90244844 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. TNFRSF9 levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90244845 Genome-wide genotyping array 2023-09-07 36865558 Boahen CK 2023-02-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36865558 Integration of Candida albicans-induced single-cell gene expression data and secretory protein concentrations reveal genetic regulators of inflammation. TNF levels 445 European ancestry individuals NA NR [4095762] (imputed) 1 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90244846 Genome-wide genotyping array 2023-11-20 37227431 Granell R 2023-05-25 Elife www.ncbi.nlm.nih.gov/pubmed/37227431 A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifies ANXA1 as a susceptibility locus for persistent wheezing. Childhood wheezing (early-onset) 943 European ancestry cases, 5,887 European ancestry controls 40 cases, 1,557 controls NR [8057852] (imputed) 0 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90297564 Genome-wide genotyping array 2023-11-20 37227431 Granell R 2023-05-25 Elife www.ncbi.nlm.nih.gov/pubmed/37227431 A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifies ANXA1 as a susceptibility locus for persistent wheezing. Childhood wheezing (pre-school remitting) 1,482 European ancestry cases, 5,887 European ancestry controls NA NR [8057852] (imputed) 16 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90297565 Genome-wide genotyping array 2023-11-20 37227431 Granell R 2023-05-25 Elife www.ncbi.nlm.nih.gov/pubmed/37227431 A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifies ANXA1 as a susceptibility locus for persistent wheezing. Childhood wheezing (mid-childhood remitting) 603 European ancestry cases, 5,887 European ancestry controls NA NR [8057852] (imputed) 15 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90297566 Genome-wide genotyping array 2023-11-20 37227431 Granell R 2023-05-25 Elife www.ncbi.nlm.nih.gov/pubmed/37227431 A meta-analysis of genome-wide association studies of childhood wheezing phenotypes identifies ANXA1 as a susceptibility locus for persistent wheezing. Childhood wheezing (late-onset) 652 European ancestry cases, 5,887 European ancestry controls NA NR [8057852] (imputed) 22 wheezing http://www.ebi.ac.uk/efo/EFO_0009715 GCST90297567 Genome-wide genotyping array 2023-11-08 35149777 Reid JG 2022-02-11 Pharmacogenomics J www.ncbi.nlm.nih.gov/pubmed/35149777 UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. Bilirubin levels in sarilumab-treated rheumatoid arthritis patients 755 European, Hispanic or Latin American, African, Asian and unknown ancestry individuals NA Illumina [NR] (imputed) 1 bilirubin measurement, response to xenobiotic stimulus http://www.ebi.ac.uk/efo/EFO_0004570, http://purl.obolibrary.org/obo/GO_0009410 GCST90103787 Genome-wide genotyping array, Exome-wide sequencing 2023-12-01 37985819 An U 2023-11-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37985819 Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Direct bilirubin levels (UKB data field 30660) 285,405 British ancestry individuals NA Affymetrix [5776313] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90277451 Genome-wide genotyping array 2023-12-01 37985819 An U 2023-11-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37985819 Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Ever taken cannabis (UKB data field 20453) 337,126 British ancestry individuals NA Affymetrix [5776313] (imputed) 0 Cannabis use http://www.ebi.ac.uk/efo/EFO_0007585 GCST90277452 Genome-wide genotyping array 2023-12-01 37985819 An U 2023-11-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37985819 Deep learning-based phenotype imputation on population-scale biobank data increases genetic discoveries. Major depressive disorder (lifetime) 337,126 British ancestry individuals NA Affymetrix [5776313] (imputed) 0 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90277450 Genome-wide genotyping array 2023-09-19 37146008 Mascheretti S 2023-05-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/37146008 Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis. Pain 352 individuals NA Illumina [4385954] (imputed) 8 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90281295 Genome-wide genotyping array 2023-09-19 37146008 Mascheretti S 2023-05-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/37146008 Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis. Anxiety 352 individuals NA Illumina [4385954] (imputed) 12 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90281296 Genome-wide genotyping array 2023-09-19 37146008 Mascheretti S 2023-05-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/37146008 Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis. Pain 754 individuals NA Illumina [5129426] (imputed) 4 pain http://www.ebi.ac.uk/efo/EFO_0003843 GCST90281297 Genome-wide genotyping array 2023-09-19 37146008 Mascheretti S 2023-05-05 PLoS One www.ncbi.nlm.nih.gov/pubmed/37146008 Adolescent anxiety and pain problems: A joint, genome-wide investigation and pathway-based analysis. Anxiety 754 individuals NA Illumina [5129426] (imputed) 5 anxiety http://www.ebi.ac.uk/efo/EFO_0005230 GCST90281298 Genome-wide genotyping array 2023-12-14 38036781 He Y 2023-11-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/38036781 East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. Peptic ulcer disease 29,739 Japanese ancestry cases, 240,675 Japanese ancestry controls NA NR [13836101] (imputed) 17 peptic ulcer disease http://purl.obolibrary.org/obo/MONDO_0004247 GCST90270926 Genome-wide genotyping array 2023-12-14 38036781 He Y 2023-11-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/38036781 East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. Gastric ulcer 20,972 Japanese ancestry cases, 240,675 Japanese ancestry controls NA NR [13822304] (imputed) 8 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90270927 Genome-wide genotyping array 2023-12-14 38036781 He Y 2023-11-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/38036781 East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. Duodenal ulcer 11,964 Japanese ancestry cases, 240,675 Japanese ancestry controls NA NR [13810785] (imputed) 19 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90270928 Genome-wide genotyping array 2023-12-14 38036781 He Y 2023-11-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/38036781 East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. Comorbidity of gastric and duodenal ulcers 3,197 Japanese ancestry cases, 240,675 Japanese ancestry controls NA NR [13795352] (imputed) 4 duodenal ulcer, gastric ulcer http://www.ebi.ac.uk/efo/EFO_0004607, http://www.ebi.ac.uk/efo/EFO_0009454 GCST90270929 Genome-wide genotyping array 2023-12-14 38036781 He Y 2023-11-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/38036781 East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. Peptic ulcer disease 29,739 Japanese ancestry cases, 240,675 Japanese ancestry controls, 22,293 European ancestry cases, 664,669 European ancestry controls NA NR [19078654] (imputed) 23 peptic ulcer disease http://purl.obolibrary.org/obo/MONDO_0004247 GCST90270930 Genome-wide genotyping array 2023-12-14 38036781 He Y 2023-11-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/38036781 East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. Gastric ulcer 20,972 Japanese ancestry cases, 240,675 Japanese ancestry controls, 7,710 European ancestry cases, 626,533 European ancestry controls NA NR [19018413] (imputed) 10 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90270931 Genome-wide genotyping array 2023-12-14 38036781 He Y 2023-11-30 Nat Genet www.ncbi.nlm.nih.gov/pubmed/38036781 East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease. Duodenal ulcer 11,964 Japanese ancestry cases, 240,675 Japanese ancestry controls, 5,153 European ancestry cases, 626,533 European ancestry controls NA NR [19009727] (imputed) 24 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90270932 Genome-wide genotyping array 2023-11-15 37156394 Ozeki T 2023-05-06 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37156394 Association of Genetic Variants of HLA-DQA1 with Bullous Pemphigoid Induced by Dipeptidyl Peptidase-4 Inhibitors. Bullous pemphigoid 90 Japanese ancestry cases, 737 Japanese ancestry controls 20 Japanese ancestry cases, 164 Japanese ancestry controls Illumina [526267] 2 bullous pemphigoid http://www.ebi.ac.uk/efo/EFO_0007187 GCST90296384 Genome-wide genotyping array 2023-11-15 37156394 Ozeki T 2023-05-06 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37156394 Association of Genetic Variants of HLA-DQA1 with Bullous Pemphigoid Induced by Dipeptidyl Peptidase-4 Inhibitors. Noninflammatory bullous pemphigoid in response to dipeptidyl peptidase-4 inhibitors 21 Japanese ancestry cases, 737 Japanese ancestry controls 8 Japanese ancestry cases, 164 Japanese ancestry controls Illumina [526267] 4 bullous pemphigoid http://www.ebi.ac.uk/efo/EFO_0007187 GCST90296385 Genome-wide genotyping array 2023-11-15 37156394 Ozeki T 2023-05-06 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37156394 Association of Genetic Variants of HLA-DQA1 with Bullous Pemphigoid Induced by Dipeptidyl Peptidase-4 Inhibitors. Inflammatory bullous pemphigoid in response to dipeptidyl peptidase-4 inhibitors 9 Japanese ancestry cases, 737 Japanese ancestry controls 2 Japanese ancestry cases, 164 Japanese ancestry controls Illumina [526267] 2 bullous pemphigoid http://www.ebi.ac.uk/efo/EFO_0007187 GCST90296386 Genome-wide genotyping array 2023-11-15 37156394 Ozeki T 2023-05-06 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37156394 Association of Genetic Variants of HLA-DQA1 with Bullous Pemphigoid Induced by Dipeptidyl Peptidase-4 Inhibitors. Conventional bullous pemphigoid 60 Japanese ancestry cases, 737 Japanese ancestry controls 10 Japanese ancestry cases, 164 Japanese ancestry controls Illumina [526267] 3 bullous pemphigoid http://www.ebi.ac.uk/efo/EFO_0007187 GCST90296387 Genome-wide genotyping array 2023-11-15 37156394 Ozeki T 2023-05-06 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37156394 Association of Genetic Variants of HLA-DQA1 with Bullous Pemphigoid Induced by Dipeptidyl Peptidase-4 Inhibitors. Bullous pemphigoid (except dipeptidyl peptidase-4 inhibitor-induced noninflammatory) 69 Japanese ancestry cases, 737 Japanese ancestry controls 12 Japanese ancestry cases, 164 Japanese ancestry controls Illumina [526267] 3 bullous pemphigoid http://www.ebi.ac.uk/efo/EFO_0007187 GCST90296388 Genome-wide genotyping array 2023-09-22 37165447 De Angelis F 2023-05-11 Genome Med www.ncbi.nlm.nih.gov/pubmed/37165447 Sex differences in the polygenic architecture of hearing problems in adults. Hearing problems 501,825 European ancestry individuals 226,043 European ancestry individuals, 6,636 African ancestry individuals, 980 admixed American ancestry individuals, 8,876 Central Asian ancestry, South Asian ancestry individuals, 2,709 East Asian ancestry individuals, 1,599 Middle Eastern ancestry individuals NR [5331308] (imputed) 14 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90292534 Genome-wide genotyping array 2023-09-22 37165447 De Angelis F 2023-05-11 Genome Med www.ncbi.nlm.nih.gov/pubmed/37165447 Sex differences in the polygenic architecture of hearing problems in adults. Hearing problems 223,081 European ancestry males NA NR [5331308] (imputed) 15 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90292535 Genome-wide genotyping array 2023-09-22 37165447 De Angelis F 2023-05-11 Genome Med www.ncbi.nlm.nih.gov/pubmed/37165447 Sex differences in the polygenic architecture of hearing problems in adults. Hearing problems 278,744 European ancestry females NA NR [5331308] (imputed) 24 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90292536 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 1,507 Asian ancestry cases, 8,687 Asian ancestry controls NA Affymetrix [11631871] (imputed) 8 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134289 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 140,025 European ancestry cases, 344,349 European ancestry controls, 140,025 South Asian ancestry cases, 344,349 South Asian ancestry controls, 140,025 East Asian ancestry cases, 344,349 East Asian ancestry controls, 140,025 African ancestry cases, 344,349 African ancestry controls, 140,025 Hispanic or Latin American cases, 344,349 Hispanic or Latin American controls NA Affymetrix [11429803] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134290 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 119,351 European ancestry individuals NA Affymetrix [MVP Axiom Array] (imputed) 20 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90296701 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 28,565 African American individuals NA Affymetrix [MVP Axiom Array] (imputed) 16 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90296702 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 1,328 Asian ancestry individuals NA Affymetrix [MVP Axiom Array] (imputed) 2 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90296703 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 5,561 Hispanic or Latin American cases, 4,766 Hispanic or Latin American controls NA Affymetrix [MVP Axiom Array] (imputed) 4 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90296704 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 163,015 European ancestry, African American, Asian ancestry, Hispanic or Latin American and unknown ancestry individuals NA Affymetrix [MVP Axiom Array] (imputed) 5 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90296705 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 54,039 European ancestry cases, 239,780 European ancestry controls NA Affymetrix [24880768] (imputed) 61 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134279 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 984 South Asian ancestry cases, 6,178 South Asian ancestry controls NA Affymetrix [21531151] (imputed) 6 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134280 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 121 East Asian ancestry cases, 1,583 East Asian ancestry controls NA Affymetrix [14972686] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134281 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 862 African ancestry cases, 6,326 African ancestry controls NA Affymetrix [22154154] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134282 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 58,574 European ancestry cases, 262,785 European ancestry controls, 58,574 South Asian ancestry cases, 262,785 South Asian ancestry controls, 58,574 East Asian ancestry cases, 262,785 East Asian ancestry controls, 58,574 African ancestry cases, 262,785 African ancestry controls NA Affymetrix [30763938] (imputed) 0 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134283 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 79,569 European ancestry cases, 80,002 European ancestry controls, 79,569 African American cases, 80,002 African American controls, 79,569 Asian ancestry cases, 80,002 Asian ancestry controls, 79,569 Hispanic or Latin American cases, 80,002 Hispanic or Latin American controls NA Affymetrix [MVP Axiom Array] (imputed) 1 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90296706 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 58,574 European ancestry cases, 262,785 European ancestry controls, 58,574 South Asian ancestry cases, 262,785 South Asian ancestry controls, 58,574 East Asian ancestry cases, 262,785 East Asian ancestry controls, 58,574 African ancestry cases, 262,785 African ancestry controls NA Affymetrix [30763938] (imputed) 26 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134285 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 140,025 European ancestry cases, 344,349 European ancestry controls, 140,025 South Asian ancestry cases, 344,349 South Asian ancestry controls, 140,025 East Asian ancestry cases, 344,349 East Asian ancestry controls, 140,025 African ancestry cases, 344,349 African ancestry controls, 140,025 Hispanic or Latin American cases, 344,349 Hispanic or Latin American controls NA Affymetrix [19503252] (imputed) 27 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134284 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 133,506 European ancestry cases, 335,938 European ancestry controls, 133,506 South Asian ancestry cases, 335,938 South Asian ancestry controls, 133,506 East Asian ancestry cases, 335,938 East Asian ancestry controls, 133,506 African ancestry cases, 335,938 African ancestry controls, 133,506 Hispanic or Latin American cases, 335,938 Hispanic or Latin American controls NA Affymetrix [9339732] (imputed) 60 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134286 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 17,275 African ancestry cases, 18,478 African ancestry controls NA Affymetrix [18883719] (imputed) 13 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134287 Genome-wide genotyping array 2023-11-07 36411363 McDonald MN 2022-11-21 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36411363 Novel genetic loci associated with osteoarthritis in multi-ancestry analyses in the Million Veteran Program and UK Biobank. Osteoarthritis 109,358 European ancestry cases, 303,812 European ancestry controls NA Affymetrix [14034269] (imputed) 74 osteoarthritis http://purl.obolibrary.org/obo/MONDO_0005178 GCST90134288 Genome-wide genotyping array 2023-10-12 37704630 Lee J 2023-09-13 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37704630 Quantifying the causal impact of biological risk factors on healthcare costs. Annual healthcare cost 373,160 European ancestry individuals NA Illumina [20170172] (imputed) 38 wellbeing measurement http://www.ebi.ac.uk/efo/EFO_0007869 GCST90292604 Genome-wide genotyping array 2023-10-12 32210231 Hollis B 2020-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32210231 Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan. Male puberty timing (early vs. average onset facial hair) 13,226 European ancestry early onset individuals, 161,175 European ancestry average onset individuals NA NR [7400000] (imputed) 32 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST90012084 Genome-wide genotyping array 2023-10-12 32210231 Hollis B 2020-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32210231 Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan. Male puberty timing (late vs. average onset facial hair) 26,066 European ancestry late onset individuals, 161,175 European ancestry average onset individuals NA NR [7400000] (imputed) 41 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST90012085 Genome-wide genotyping array 2023-10-12 32210231 Hollis B 2020-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32210231 Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan. Male puberty timing (early vs. average onset voice breaking) 8,245 European ancestry early onset individuals, 172,138 European ancestry average onset individuals NA NR [7400000] (imputed) 18 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST90012086 Genome-wide genotyping array 2023-10-12 32210231 Hollis B 2020-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32210231 Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan. Male puberty timing (late vs. average onset voice breaking) 11,334 European ancestry late onset individuals, 172,138 European ancestry average onset individuals NA NR [7400000] (imputed) 21 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST90012087 Genome-wide genotyping array 2023-10-12 32210231 Hollis B 2020-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/32210231 Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan. Male puberty timing (age at voice breaking MTAG) 205,354 European ancestry individuals NA NR [7400000] (imputed) 76 puberty onset measurement http://www.ebi.ac.uk/efo/EFO_0005677 GCST90012088 Genome-wide genotyping array 2023-07-12 36986172 Zhang Z 2023-03-16 Nutrients www.ncbi.nlm.nih.gov/pubmed/36986172 Non-Alcoholic Fatty Liver Disease and Vitamin D in the UK Biobank: A Two-Sample Bidirectional Mendelian Randomisation Study. Nonalcoholic fatty liver disease 2,757 European ancestry cases, 460,161 European ancestry controls NA NR [11324872] 5 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90271929 Genome-wide genotyping array 2023-07-12 36986172 Zhang Z 2023-03-16 Nutrients www.ncbi.nlm.nih.gov/pubmed/36986172 Non-Alcoholic Fatty Liver Disease and Vitamin D in the UK Biobank: A Two-Sample Bidirectional Mendelian Randomisation Study. Nonalcoholic fatty liver disease (without other liver diseases) 1,747 European ancestry cases, 448,282 European ancestry controls NA NR [10788717] 0 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90271930 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I27: Other pulmonary heart diseases 2,310 Chinese ancestry cases, 75,133 Chinese ancestry controls NA Affymetrix [8993425] (imputed) 0 cardiovascular disease http://www.ebi.ac.uk/efo/EFO_0000319 GCST90246087 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I38: Endocarditis, valve unspecified 131 Chinese ancestry cases, 75,769 Chinese ancestry controls NA Affymetrix [6918660] (imputed) 0 endocarditis http://www.ebi.ac.uk/efo/EFO_0000465 GCST90246088 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I42: Cardiomyopathy 209 Chinese ancestry cases, 75,742 Chinese ancestry controls NA Affymetrix [7528832] (imputed) 0 cardiomyopathy http://www.ebi.ac.uk/efo/EFO_0000318 GCST90246089 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I46: Cardiac arrest 404 Chinese ancestry cases, 75,649 Chinese ancestry controls NA Affymetrix [8320741] (imputed) 0 GCST90246090 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I48: Atrial fibrillation and flutter 227 Chinese ancestry cases, 75,694 Chinese ancestry controls NA Affymetrix [7632221] (imputed) 1 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90246091 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I49: Other cardiac arrhythmias 1,480 Chinese ancestry cases, 74,855 Chinese ancestry controls NA Affymetrix [8986450] (imputed) 0 cardiac arrhythmia http://www.ebi.ac.uk/efo/EFO_0004269 GCST90246092 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I50: Heart failure 1,467 Chinese ancestry cases, 75,149 Chinese ancestry controls NA Affymetrix [8986450] (imputed) 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90246093 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I51: Complications and ill-defined descriptions of heart disease 730 Chinese ancestry cases, 75,424 Chinese ancestry controls NA Affymetrix [8868354] (imputed) 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90246094 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I60: Nontraumatic subarachnoid hemorrhage 602 Chinese ancestry cases, 75,712 Chinese ancestry controls NA Affymetrix [8752703] (imputed) 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90246095 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I61: Nontraumatic intracerebral hemorrhage 6,663 Chinese ancestry cases, 74,585 Chinese ancestry controls NA Affymetrix [8998219] (imputed) 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90246096 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I62: Other and unspecified nontraumatic intracranial hemorrhage 144 Chinese ancestry cases, 75,761 Chinese ancestry controls NA Affymetrix [7048602] (imputed) 0 intracranial hemorrhage http://www.ebi.ac.uk/efo/EFO_0000551 GCST90246097 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I63: Cerebral infarction 14,302 Chinese ancestry cases, 67,954 Chinese ancestry controls NA Affymetrix [8999500] (imputed) 1 brain infarction http://www.ebi.ac.uk/efo/EFO_0004277 GCST90246098 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I64: Stroke, not specified as haemorrhage or infarction 876 Chinese ancestry cases, 75,346 Chinese ancestry controls NA Affymetrix [8930856] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90246099 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I65: Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction 147 Chinese ancestry cases, 75,749 Chinese ancestry controls NA Affymetrix [7076584] (imputed) 0 occlusion precerebral artery http://www.ebi.ac.uk/efo/EFO_0009677 GCST90246100 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I65: Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction 791 Chinese ancestry cases, 75,463 Chinese ancestry controls NA Affymetrix [8900463] (imputed) 0 occlusion precerebral artery http://www.ebi.ac.uk/efo/EFO_0009677 GCST90246101 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I67: Other cerebrovascular diseases 7,155 Chinese ancestry cases, 71,306 Chinese ancestry controls NA Affymetrix [8997558] (imputed) 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90246102 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I69: Sequelae of cerebrovascular disease 2,220 Chinese ancestry cases, 74,957 Chinese ancestry controls NA Affymetrix [8992746] (imputed) 0 cerebrovascular disorder http://www.ebi.ac.uk/efo/EFO_0003763 GCST90246103 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I70: Atherosclerosis 563 Chinese ancestry cases, 75,577 Chinese ancestry controls NA Affymetrix [8697377] (imputed) 0 atherosclerosis http://www.ebi.ac.uk/efo/EFO_0003914 GCST90246104 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I83: Varicose veins of lower extremities 376 Chinese ancestry cases, 75,545 Chinese ancestry controls NA Affymetrix [8235744] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90246105 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J02: Acute pharyngitis 186 Chinese ancestry cases, 75,723 Chinese ancestry controls NA Affymetrix [7383357] (imputed) 0 acute pharyngitis http://www.ebi.ac.uk/efo/EFO_0009657 GCST90246106 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J03: Acute tonsillitis 195 Chinese ancestry cases, 75,720 Chinese ancestry controls NA Affymetrix [7443675] (imputed) 0 Recurrent tonsillitis http://purl.obolibrary.org/obo/HP_0011110 GCST90246107 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J04: Acute laryngitis and tracheitis 138 Chinese ancestry cases, 75,773 Chinese ancestry controls NA Affymetrix [6991069] (imputed) 0 acute laryngitis http://purl.obolibrary.org/obo/MONDO_0004777 GCST90246108 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J06: Acute upper respiratory infections of multiple and unspecified sites 1,114 Chinese ancestry cases, 75,154 Chinese ancestry controls NA Affymetrix [8970168] (imputed) 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90246109 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Pneumonia due to Streptococcus pneumoniae (Union J13) 124 Chinese ancestry cases, 75,774 Chinese ancestry controls NA Affymetrix [6841415] (imputed) 0 pneumococcal infection http://www.ebi.ac.uk/efo/EFO_0000772 GCST90246110 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J15: Bacterial pneumonia, not elsewhere classified 221 Chinese ancestry cases, 75,694 Chinese ancestry controls NA Affymetrix [7597824] (imputed) 0 bacterial pneumonia http://www.ebi.ac.uk/efo/EFO_1001272 GCST90246111 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J18: Pneumonia, unspecified organism 6,903 Chinese ancestry cases, 71,487 Chinese ancestry controls NA Affymetrix [8997197] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90246112 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J20: Acute bronchitis 1,765 Chinese ancestry cases, 74,675 Chinese ancestry controls NA Affymetrix [8990201] (imputed) 0 Acute bronchitis http://purl.obolibrary.org/obo/HP_0012388 GCST90246113 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J31: Chronic rhinitis, nasopharyngitis and pharyngitis 123 Chinese ancestry cases, 75,754 Chinese ancestry controls NA Affymetrix [6830139] (imputed) 0 rhinitis http://www.ebi.ac.uk/efo/EFO_0008521 GCST90246114 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J32: Chronic sinusitis 207 Chinese ancestry cases, 75,680 Chinese ancestry controls NA Affymetrix [7517125] (imputed) 0 sinusitis http://www.ebi.ac.uk/efo/EFO_0007486 GCST90246115 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J33: Nasal polyp 125 Chinese ancestry cases, 75,745 Chinese ancestry controls NA Affymetrix [6853435] (imputed) 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90246116 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J34: Other and unspecified disorders of nose and nasal sinuses 141 Chinese ancestry cases, 75,744 Chinese ancestry controls NA Affymetrix [7020050] (imputed) 0 paranasal sinus disease http://www.ebi.ac.uk/efo/EFO_0009481 GCST90246117 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J38: Diseases of vocal cords and larynx, not elsewhere classified 155 Chinese ancestry cases, 75,718 Chinese ancestry controls NA Affymetrix [7145397] (imputed) 0 laryngeal disease http://www.ebi.ac.uk/efo/EFO_0009673 GCST90246118 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J40: Bronchitis, not specified as acute or chronic 1,319 Chinese ancestry cases, 75,017 Chinese ancestry controls NA Affymetrix [8982181] (imputed) 0 bronchial disease http://www.ebi.ac.uk/efo/EFO_1002018 GCST90246119 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J42: Unspecified chronic bronchitis 4,046 Chinese ancestry cases, 74,460 Chinese ancestry controls NA Affymetrix [8995866] (imputed) 0 chronic bronchitis http://www.ebi.ac.uk/efo/EFO_0006505 GCST90246120 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J43: Emphysema 1,666 Chinese ancestry cases, 75,363 Chinese ancestry controls NA Affymetrix [8989513] (imputed) 0 emphysema http://www.ebi.ac.uk/efo/EFO_0000464 GCST90246121 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J44: Other chronic obstructive pulmonary disease 6,043 Chinese ancestry cases, 73,676 Chinese ancestry controls NA Affymetrix [8996882] (imputed) 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90246122 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J45: Asthma 878 Chinese ancestry cases, 75,424 Chinese ancestry controls NA Affymetrix [8931333] (imputed) 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90246123 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J47: Bronchiectasis 435 Chinese ancestry cases, 75,605 Chinese ancestry controls NA Affymetrix [8407796] (imputed) 0 bronchiectasis http://purl.obolibrary.org/obo/MONDO_0004822 GCST90246124 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J84: Other interstitial pulmonary diseases 155 Chinese ancestry cases, 75,755 Chinese ancestry controls NA Affymetrix [7145429] (imputed) 0 interstitial lung disease http://www.ebi.ac.uk/efo/EFO_0004244 GCST90246125 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J90: Pleural effusion, not elsewhere classified 254 Chinese ancestry cases, 75,692 Chinese ancestry controls NA Affymetrix [7767613] (imputed) 0 pleural effusion http://www.ebi.ac.uk/efo/EFO_0009637 GCST90246126 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Pneumothorax (Union J93) 113 Chinese ancestry cases, 75,801 Chinese ancestry controls NA Affymetrix [6708006] (imputed) 0 pneumothorax http://purl.obolibrary.org/obo/MONDO_0002076 GCST90246127 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J96: Respiratory failure, not elsewhere classified 543 Chinese ancestry cases, 75,598 Chinese ancestry controls NA Affymetrix [8663951] (imputed) 0 respiratory failure http://www.ebi.ac.uk/efo/EFO_0009686 GCST90246128 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 J98: other respiratory problems 413 Chinese ancestry cases, 75,591 Chinese ancestry controls NA Affymetrix [8346616] (imputed) 0 respiratory system disease http://www.ebi.ac.uk/efo/EFO_0000684 GCST90246129 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K21: Gastro-esophageal reflux disease 117 Chinese ancestry cases, 75,782 Chinese ancestry controls NA Affymetrix [6758654] (imputed) 0 gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003948 GCST90246130 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K25: Gastric ulcer 525 Chinese ancestry cases, 75,499 Chinese ancestry controls NA Affymetrix [8630382] (imputed) 0 gastric ulcer http://www.ebi.ac.uk/efo/EFO_0009454 GCST90246131 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K26: Duodenal ulcer 225 Chinese ancestry cases, 75,688 Chinese ancestry controls NA Affymetrix [7620762] (imputed) 0 duodenal ulcer http://www.ebi.ac.uk/efo/EFO_0004607 GCST90246132 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K27: Peptic ulcer, site unspecified 226 Chinese ancestry cases, 75,709 Chinese ancestry controls NA Affymetrix [7626536] (imputed) 0 Peptic ulcer http://purl.obolibrary.org/obo/HP_0004398 GCST90246133 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K29: Gastritis and duodenitis 3,611 Chinese ancestry cases, 73,433 Chinese ancestry controls NA Affymetrix [8995518] (imputed) 0 gastritis http://www.ebi.ac.uk/efo/EFO_0000217 GCST90246134 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Dyspepsia (Union K30) 568 Chinese ancestry cases, 75,494 Chinese ancestry controls NA Affymetrix [8705081] (imputed) 0 dyspepsia http://www.ebi.ac.uk/efo/EFO_0008533 GCST90246135 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 K31: Other diseases of stomach and duodenum 344 Chinese ancestry cases, 75,574 Chinese ancestry controls NA Affymetrix [8129578] (imputed) 0 digestive system disease http://www.ebi.ac.uk/efo/EFO_0000405 GCST90246136 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C85.7: Other specified types of non-Hodgkin lymphoma 189 Chinese ancestry cases, 75,705 Chinese ancestry controls NA Affymetrix [7404344] (imputed) 0 non-Hodgkins lymphoma http://www.ebi.ac.uk/efo/EFO_0005952 GCST90246037 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Leukaemia of unspecified cell type (Union C95) 118 Chinese ancestry cases, 75,771 Chinese ancestry controls NA Affymetrix [6771087] (imputed) 0 leukemia http://www.ebi.ac.uk/efo/EFO_0000565 GCST90246038 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 D17: Benign lipomatous neoplasm 185 Chinese ancestry cases, 75,700 Chinese ancestry controls NA Affymetrix [7376020] (imputed) 0 benign lipomatous neoplasm http://purl.obolibrary.org/obo/MONDO_0044983 GCST90246039 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 D24: Benign neoplasm of breast 131 Chinese ancestry cases, 45,203 Chinese ancestry controls NA Affymetrix [6916491] (imputed) 0 benign neoplasm http://www.ebi.ac.uk/efo/EFO_0002422 GCST90246040 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 D25: Leiomyoma of uterus 877 Chinese ancestry cases, 44,550 Chinese ancestry controls NA Affymetrix [8929108] (imputed) 0 uterine fibroid http://www.ebi.ac.uk/efo/EFO_0000731 GCST90246041 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Other benign neoplasms of uterus (Union D26) 185 Chinese ancestry cases, 45,155 Chinese ancestry controls NA Affymetrix [7374735] (imputed) 0 uterine neoplasm http://www.ebi.ac.uk/efo/EFO_0003859 GCST90246042 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Benign neoplasm of eye and adnexa (Union D31) 184 Chinese ancestry cases, 75,688 Chinese ancestry controls NA Affymetrix [7368945] (imputed) 0 benign neoplasm of eye http://purl.obolibrary.org/obo/MONDO_0021454 GCST90246043 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Neoplasm of uncertain or unknown behaviour of middle ear and respiratory and intrathoracic organs (Union D38) 113 Chinese ancestry cases, 75,761 Chinese ancestry controls NA Affymetrix [6707997] (imputed) 0 respiratory system neoplasm http://www.ebi.ac.uk/efo/EFO_0003853 GCST90246044 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Neoplasm of uncertain or unknown behaviour of endocrine glands (Union D44) 130 Chinese ancestry cases, 75,734 Chinese ancestry controls NA Affymetrix [6908096] (imputed) 0 endocrine neoplasm http://www.ebi.ac.uk/efo/EFO_0003769 GCST90246045 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 D48: Neoplasm of uncertain behavior of other and unspecified sites 147 Chinese ancestry cases, 75,740 Chinese ancestry controls NA Affymetrix [7076527] (imputed) 0 GCST90246046 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 D50: iron deficiency anaemia 128 Chinese ancestry cases, 75,752 Chinese ancestry controls NA Affymetrix [6886551] (imputed) 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90246047 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 D64: Other anemias 409 Chinese ancestry cases, 75,578 Chinese ancestry controls NA Affymetrix [8335397] (imputed) 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90246048 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 D69: Purpura and other hemorrhagic conditions 161 Chinese ancestry cases, 75,734 Chinese ancestry controls NA Affymetrix [7194411] (imputed) 0 hemorrhagic disease http://purl.obolibrary.org/obo/MONDO_0002243 GCST90246049 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 E04: Other nontoxic goiter 433 Chinese ancestry cases, 75,497 Chinese ancestry controls NA Affymetrix [8402303] (imputed) 1 nontoxic goiter http://purl.obolibrary.org/obo/MONDO_0001658 GCST90246050 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 E05: Thyrotoxicosis [hyperthyroidism] 118 Chinese ancestry cases, 75,758 Chinese ancestry controls NA Affymetrix [6771106] (imputed) 0 Thyrotoxicosis http://www.ebi.ac.uk/efo/EFO_0009190 GCST90246051 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Insulin-dependent diabetes mellitus (Union E10) 206 Chinese ancestry cases, 75,729 Chinese ancestry controls NA Affymetrix [7511205] (imputed) 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90246052 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Non-insulin-dependent diabetes mellitus (Union E11) 4,528 Chinese ancestry cases, 72,650 Chinese ancestry controls NA Affymetrix [8996068] (imputed) 7 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90246053 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 E14: Unspecified diabetes mellitus 4,382 Chinese ancestry cases, 72,812 Chinese ancestry controls NA Affymetrix [8996201] (imputed) 6 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90246054 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 E78: Disorders of lipoprotein metabolism and other lipidemias 665 Chinese ancestry cases, 75,430 Chinese ancestry controls NA Affymetrix [8820191] (imputed) 0 Hypercholesterolemia http://purl.obolibrary.org/obo/HP_0003124 GCST90246055 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 E87: Other disorders of fluid, electrolyte and acid-base balance 616 Chinese ancestry cases, 75,513 Chinese ancestry controls NA Affymetrix [8769588] (imputed) 0 Abnormality of metabolism/homeostasis http://purl.obolibrary.org/obo/HP_0001939 GCST90246056 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 F20: Schizophrenia 146 Chinese ancestry cases, 75,733 Chinese ancestry controls NA Affymetrix [7067535] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90246057 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 F32: Major depressive disorder, single episode 119 Chinese ancestry cases, 75,752 Chinese ancestry controls NA Affymetrix [6783221] (imputed) 0 major depressive episode http://www.ebi.ac.uk/efo/EFO_0007634 GCST90246058 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 F45: Somatoform disorders 116 Chinese ancestry cases, 75,767 Chinese ancestry controls NA Affymetrix [6746069] (imputed) 0 somatoform disorder http://www.ebi.ac.uk/efo/EFO_0009687 GCST90246059 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Other neurotic disorders (Union F48) 152 Chinese ancestry cases, 75,748 Chinese ancestry controls NA Affymetrix [7119785] (imputed) 0 neurotic disorder http://www.ebi.ac.uk/efo/EFO_0004257 GCST90246060 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Mental disorder, not otherwise specified (Union F99) 224 Chinese ancestry cases, 75,691 Chinese ancestry controls NA Affymetrix [7615197] (imputed) 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90246061 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G20: parkinsons disease 213 Chinese ancestry cases, 75,714 Chinese ancestry controls NA Affymetrix [7551906] (imputed) 0 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90246062 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G31: Other degenerative diseases of nervous system, not elsewhere classified 261 Chinese ancestry cases, 75,705 Chinese ancestry controls NA Affymetrix [7800638] (imputed) 0 neurodegenerative disease http://www.ebi.ac.uk/efo/EFO_0005772 GCST90246063 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G40: epilepsy 217 Chinese ancestry cases, 75,737 Chinese ancestry controls NA Affymetrix [7575214] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90246064 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G44: Other headache syndromes 348 Chinese ancestry cases, 75,636 Chinese ancestry controls NA Affymetrix [8143437] (imputed) 0 headache disorder http://www.ebi.ac.uk/efo/EFO_0009550 GCST90246065 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G45: Transient cerebral ischemic attacks and related syndromes 2,742 Chinese ancestry cases, 73,812 Chinese ancestry controls NA Affymetrix [8994369] (imputed) 0 transient ischemic attack http://www.ebi.ac.uk/efo/EFO_0003764 GCST90246066 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G51: Facial nerve disorders 323 Chinese ancestry cases, 75,612 Chinese ancestry controls NA Affymetrix [8055815] (imputed) 0 facial nerve disease http://www.ebi.ac.uk/efo/EFO_1002051 GCST90246067 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G62: Other and unspecified polyneuropathies 103 Chinese ancestry cases, 75,767 Chinese ancestry controls NA Affymetrix [6571202] (imputed) 0 polyneuropathy http://www.ebi.ac.uk/efo/EFO_0009562 GCST90246068 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 G93: Other disorders of brain 123 Chinese ancestry cases, 75,796 Chinese ancestry controls NA Affymetrix [6830177] (imputed) 0 brain disease http://www.ebi.ac.uk/efo/EFO_0005774 GCST90246069 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H02: Other disorders of eyelid 109 Chinese ancestry cases, 75,772 Chinese ancestry controls NA Affymetrix [6654385] (imputed) 0 eyelid disease http://www.ebi.ac.uk/efo/EFO_0009547 GCST90246070 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H11: Other disorders of conjunctiva 492 Chinese ancestry cases, 75,494 Chinese ancestry controls NA Affymetrix [8556173] (imputed) 0 Conjunctival Disorder http://www.ebi.ac.uk/efo/EFO_1000203 GCST90246071 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H16: Keratitis 165 Chinese ancestry cases, 75,728 Chinese ancestry controls NA Affymetrix [7226548] (imputed) 0 keratitis http://www.ebi.ac.uk/efo/EFO_0009449 GCST90246072 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H25: Age-related cataract 1,305 Chinese ancestry cases, 74,898 Chinese ancestry controls NA Affymetrix [8981635] (imputed) 0 Age-related cataract http://purl.obolibrary.org/obo/HP_0011141 GCST90246073 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H26: Other cataract 2,693 Chinese ancestry cases, 74,019 Chinese ancestry controls NA Affymetrix [8994153] (imputed) 0 cataract http://purl.obolibrary.org/obo/MONDO_0005129 GCST90246074 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H33: Retinal detachments and breaks 148 Chinese ancestry cases, 75,729 Chinese ancestry controls NA Affymetrix [7085576] (imputed) 0 retinal detachment http://www.ebi.ac.uk/efo/EFO_0005773 GCST90246075 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H35: Other retinal disorders 225 Chinese ancestry cases, 75,679 Chinese ancestry controls NA Affymetrix [7620759] (imputed) 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90246076 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H40: Glaucoma 385 Chinese ancestry cases, 75,568 Chinese ancestry controls NA Affymetrix [8264048] (imputed) 1 glaucoma http://purl.obolibrary.org/obo/MONDO_0005041 GCST90246077 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H43: Disorders of vitreous body 105 Chinese ancestry cases, 75,782 Chinese ancestry controls NA Affymetrix [6599782] (imputed) 1 vitreous body disease http://www.ebi.ac.uk/efo/EFO_0008624 GCST90246078 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H81: Disorders of vestibular function 580 Chinese ancestry cases, 75,464 Chinese ancestry controls NA Affymetrix [8722951] (imputed) 0 vestibular disease http://www.ebi.ac.uk/efo/EFO_0009691 GCST90246079 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 H91.8: Other specified hearing loss 249 Chinese ancestry cases, 75,712 Chinese ancestry controls NA Affymetrix [7743514] (imputed) 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90246080 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I10: Essential (primary) hypertension 12,298 Chinese ancestry cases, 69,440 Chinese ancestry controls NA Affymetrix [8999693] (imputed) 2 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90246081 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Hypertensive heart disease (Union I11) 453 Chinese ancestry cases, 75,614 Chinese ancestry controls NA Affymetrix [8456687] (imputed) 0 hypertensive heart disease http://purl.obolibrary.org/obo/MONDO_0001302 GCST90246082 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I20: Angina pectoris 1,380 Chinese ancestry cases, 75,111 Chinese ancestry controls NA Affymetrix [8984048] (imputed) 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90246083 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I21: Acute myocardial infarction 3,386 Chinese ancestry cases, 74,689 Chinese ancestry controls NA Affymetrix [8996038] (imputed) 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90246084 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I24: Other acute ischemic heart diseases 218 Chinese ancestry cases, 75,727 Chinese ancestry controls NA Affymetrix [7580988] (imputed) 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90246085 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 I25: Chronic ischemic heart disease 13,050 Chinese ancestry cases, 68,051 Chinese ancestry controls NA Affymetrix [8999184] (imputed) 0 heart disease http://www.ebi.ac.uk/efo/EFO_0003777 GCST90246086 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 A09: Infectious gastroenteritis and colitis, unspecified 1,768 Chinese ancestry cases, 74,748 Chinese ancestry controls NA Affymetrix [8990299] (imputed) 0 viral disease, intestinal disease http://www.ebi.ac.uk/efo/EFO_0000763, http://www.ebi.ac.uk/efo/EFO_0009431 GCST90246012 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Respiratory tuberculosis/bacteriologically and histologically confirmed (Union A15) 187 Chinese ancestry cases, 75,761 Chinese ancestry controls NA Affymetrix [7390615] (imputed) 0 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90246013 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Respiratory tuberculosis, not confirmed bacteriologically or histologically (Union A16) 488 Chinese ancestry cases, 75,529 Chinese ancestry controls NA Affymetrix [8546202] (imputed) 0 pulmonary tuberculosis http://www.ebi.ac.uk/efo/EFO_1000049 GCST90246014 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Tuberculosis of other organs (Union A18) 123 Chinese ancestry cases, 75,762 Chinese ancestry controls NA Affymetrix [6830130] (imputed) 0 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90246015 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 B02: Zoster [herpes zoster] 549 Chinese ancestry cases, 75,459 Chinese ancestry controls NA Affymetrix [8674481] (imputed) 0 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST90246016 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Chronic viral hepatitis (Union B18) 252 Chinese ancestry cases, 75,652 Chinese ancestry controls NA Affymetrix [7757975] (imputed) 0 viral human hepatitis infection http://www.ebi.ac.uk/efo/EFO_0004196 GCST90246017 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 B19: infective viral hepatitis 117 Chinese ancestry cases, 75,764 Chinese ancestry controls NA Affymetrix [6758615] (imputed) 0 viral human hepatitis infection http://www.ebi.ac.uk/efo/EFO_0004196 GCST90246018 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Other and unspecified infectious diseases (Union B99) 179 Chinese ancestry cases, 75,707 Chinese ancestry controls NA Affymetrix [7333931] (imputed) 0 infectious disease http://www.ebi.ac.uk/efo/EFO_0005741 GCST90246019 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Malignant neoplasm of nasopharynx (Union C11) 113 Chinese ancestry cases, 75,760 Chinese ancestry controls NA Affymetrix [6707997] (imputed) 0 nasopharyngeal neoplasm http://www.ebi.ac.uk/efo/EFO_0004252 GCST90246020 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C15: Malignant neoplasm of esophagus 508 Chinese ancestry cases, 75,474 Chinese ancestry controls NA Affymetrix [8595059] (imputed) 0 neoplasm of esophagus http://purl.obolibrary.org/obo/MONDO_0021355 GCST90246021 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C16: Malignant neoplasm of stomach 756 Chinese ancestry cases, 75,270 Chinese ancestry controls NA Affymetrix [8883502] (imputed) 0 stomach neoplasm http://www.ebi.ac.uk/efo/EFO_0003897 GCST90246022 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C18: Malignant neoplasm of colon 434 Chinese ancestry cases, 75,513 Chinese ancestry controls NA Affymetrix [8404973] (imputed) 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90246023 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C20: Malignant neoplasm of rectum 447 Chinese ancestry cases, 75,488 Chinese ancestry controls NA Affymetrix [8440242] (imputed) 0 rectum cancer http://www.ebi.ac.uk/efo/EFO_1000657 GCST90246024 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C22: Malignant neoplasm of liver and intrahepatic bile ducts 665 Chinese ancestry cases, 75,355 Chinese ancestry controls NA Affymetrix [8820153] (imputed) 1 liver neoplasm http://www.ebi.ac.uk/efo/EFO_1001513 GCST90246025 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C25: Malignant neoplasm of pancreas 172 Chinese ancestry cases, 75,716 Chinese ancestry controls NA Affymetrix [7280425] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90246026 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C34: Malignant neoplasm of bronchus and lung 1,552 Chinese ancestry cases, 74,800 Chinese ancestry controls NA Affymetrix [8987690] (imputed) 1 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90246027 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C50: Malignant neoplasm of breast 503 Chinese ancestry cases, 44,883 Chinese ancestry controls NA Affymetrix [8578343] (imputed) 0 breast cancer http://purl.obolibrary.org/obo/MONDO_0007254 GCST90246028 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. Malignant neoplasm of cervix uteri (Union C53) 243 Chinese ancestry cases, 45,135 Chinese ancestry controls NA Affymetrix [7711861] (imputed) 0 cervical carcinoma http://www.ebi.ac.uk/efo/EFO_0001061 GCST90246029 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C54: Malignant neoplasm of corpus uteri 111 Chinese ancestry cases, 45,231 Chinese ancestry controls NA Affymetrix [6680230] (imputed) 0 uterine corpus cancer http://www.ebi.ac.uk/efo/EFO_0007532 GCST90246030 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C67: Malignant neoplasm of bladder 153 Chinese ancestry cases, 75,744 Chinese ancestry controls NA Affymetrix [7128646] (imputed) 0 urinary bladder carcinoma http://purl.obolibrary.org/obo/MONDO_0004986 GCST90246031 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C71: Malignant neoplasm of brain 122 Chinese ancestry cases, 75,775 Chinese ancestry controls NA Affymetrix [6818704] (imputed) 0 brain neoplasm http://www.ebi.ac.uk/efo/EFO_0003833 GCST90246032 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C73: Malignant neoplasm of thyroid gland 128 Chinese ancestry cases, 75,734 Chinese ancestry controls NA Affymetrix [6886564] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90246033 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C78: Secondary malignant neoplasm of respiratory and digestive organs 153 Chinese ancestry cases, 75,730 Chinese ancestry controls NA Affymetrix [7128622] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90246034 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C79: Secondary malignant neoplasm of other and unspecified sites 139 Chinese ancestry cases, 75,742 Chinese ancestry controls NA Affymetrix [7000753] (imputed) 0 secondary malignant neoplasm http://www.ebi.ac.uk/efo/EFO_0009812 GCST90246035 Genome-wide genotyping array 2023-09-28 37601966 Walters RG 2023-07-20 Cell Genom www.ncbi.nlm.nih.gov/pubmed/37601966 Genotyping and population characteristics of the China Kadoorie Biobank. ICD10 C80: Malignant neoplasm without specification of site 655 Chinese ancestry cases, 75,334 Chinese ancestry controls NA Affymetrix [8810820] (imputed) 0 GCST90246036 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Anteromedial temporal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 29 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271790 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Dorsolateral prefrontal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 48 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271791 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Dorsomedial frontal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 54 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271792 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Inferior parietal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 45 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271793 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Motor premotor area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 39 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271794 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Occipital area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 45 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271795 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Orbitofrontal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 41 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271796 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Parsopercularis area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 46 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271797 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Posterolateral temporal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 33 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271798 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Precuneus area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 34 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271799 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Superior parietal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 30 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271800 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Superior temporal area (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 39 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271801 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Dorsolateral prefrontal thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 23 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271802 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Inferior parietal thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 21 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271803 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Medial prefrontal thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 25 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271804 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Medial temporal thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 15 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271805 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Middle temporal thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 23 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271806 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Motor premotor thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 11 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271807 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Occipital thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 17 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271808 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Perisylvian thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 26 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271809 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Superior parietal thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 21 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271810 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Temporal pole thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 17 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271811 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Ventral frontal thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 29 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271812 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Ventromedial occipital thickness (unadjusted for global measures) 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 32 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271813 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Cortical surface area 32,488 European ancestry individuals 5,360 European ancestry children, 3,776 children NR [7598201] (imputed) 26 cortical surface area measurement http://www.ebi.ac.uk/efo/EFO_0010736 GCST90271814 Genome-wide genotyping array 2023-07-17 37089073 Acharya V 2023-04-23 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/37089073 Meta-analysis of age-related cognitive decline reveals a novel locus for the attention domain and implicates a COVID-19-related gene for global cognitive function. Cognitive performance (attention) (longitudinal) 3,042 European ancestry individuals aged 65 years or older NA Illumina [NR] (imputed) 19 attention function measurement http://www.ebi.ac.uk/efo/EFO_0007636 GCST90270900 Genome-wide genotyping array 2023-07-17 37089073 Acharya V 2023-04-23 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/37089073 Meta-analysis of age-related cognitive decline reveals a novel locus for the attention domain and implicates a COVID-19-related gene for global cognitive function. Cognitive performance (executive function) (longitudinal) 3,044 European ancestry individuals aged 65 years or older NA Illumina [NR] (imputed) 13 executive function measurement http://www.ebi.ac.uk/efo/EFO_0009332 GCST90270901 Genome-wide genotyping array 2023-07-17 37089073 Acharya V 2023-04-23 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/37089073 Meta-analysis of age-related cognitive decline reveals a novel locus for the attention domain and implicates a COVID-19-related gene for global cognitive function. Cognitive performance (memory) (longitudinal) 3,042 European ancestry individuals aged 65 years or older NA Illumina [NR] (imputed) 17 memory performance http://www.ebi.ac.uk/efo/EFO_0004874 GCST90270902 Genome-wide genotyping array 2023-07-17 37089073 Acharya V 2023-04-23 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/37089073 Meta-analysis of age-related cognitive decline reveals a novel locus for the attention domain and implicates a COVID-19-related gene for global cognitive function. Cognitive performance (language) (longitudinal) 3,043 European ancestry individuals aged 65 years or older NA Illumina [NR] (imputed) 21 language measurement http://www.ebi.ac.uk/efo/EFO_0007797 GCST90270903 Genome-wide genotyping array 2023-07-17 37089073 Acharya V 2023-04-23 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/37089073 Meta-analysis of age-related cognitive decline reveals a novel locus for the attention domain and implicates a COVID-19-related gene for global cognitive function. Cognitive performance (visuospatial function) (longitudinal) 2,995 European ancestry individuals aged 65 years or older NA Illumina [NR] (imputed) 18 visuospatial function measurement http://www.ebi.ac.uk/efo/EFO_0803533 GCST90270904 Genome-wide genotyping array 2023-07-17 37089073 Acharya V 2023-04-23 Alzheimers Dement www.ncbi.nlm.nih.gov/pubmed/37089073 Meta-analysis of age-related cognitive decline reveals a novel locus for the attention domain and implicates a COVID-19-related gene for global cognitive function. Cognitive performance (global cognitive function) (longitudinal) 3,013 European ancestry individuals aged 65 years or older NA Illumina [3226319] (imputed) 16 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90270905 Genome-wide genotyping array 2023-06-26 36791419 Westerman KE 2023-02-15 Diabetes www.ncbi.nlm.nih.gov/pubmed/36791419 Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits. HbA1c levels x carbohydrate intake interaction (2df) 4,328 African American individuals, 35 American Indian ancestry individuals, 122 Asian ancestry individuals, 18,214 European ancestry individuals, 7,084 Hispanic or Latin American individuals NA NR [NR] 1 carbohydrate intake measurement, HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0010811, http://www.ebi.ac.uk/efo/EFO_0004541 GCST90271343 Genome-wide sequencing 2023-06-26 36791419 Westerman KE 2023-02-15 Diabetes www.ncbi.nlm.nih.gov/pubmed/36791419 Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits. Fasting glucose levels x carbohydrate intake interaction (2df) 4,328 African American individuals, 35 American Indian ancestry individuals, 122 Asian ancestry individuals, 18,214 European ancestry individuals, 7,084 Hispanic or Latin American individuals NA NR [NR] 1 carbohydrate intake measurement, fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0010811, http://www.ebi.ac.uk/efo/EFO_0004465 GCST90271344 Genome-wide sequencing 2023-06-26 36791419 Westerman KE 2023-02-15 Diabetes www.ncbi.nlm.nih.gov/pubmed/36791419 Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits. Fasting insulin levels x carbohydrate intake interaction (2df) 4,328 African American individuals, 35 American Indian ancestry individuals, 122 Asian ancestry individuals, 18,214 European ancestry individuals, 7,084 Hispanic or Latin American individuals NA NR [NR] 1 carbohydrate intake measurement, fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0010811, http://www.ebi.ac.uk/efo/EFO_0004466 GCST90271345 Genome-wide sequencing 2023-06-26 36778599 Yu YH 2023-01-27 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/36778599 Candidate loci shared among periodontal disease, diabetes and bone density. Periodontitis / loose teeth (MTAG) at least 506,594 individuals (MTAG boosted by type 2 diabetes samples) NA NR [NR] 8 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90269796 Genome-wide genotyping array 2023-06-26 36778599 Yu YH 2023-01-27 Front Endocrinol (Lausanne) www.ncbi.nlm.nih.gov/pubmed/36778599 Candidate loci shared among periodontal disease, diabetes and bone density. Periodontitis / loose teeth (MTAG) at least 506,594 individuals (MTAG boosted by type 2 diabetes and bone mineral density samples) NA NR [NR] 7 periodontitis http://www.ebi.ac.uk/efo/EFO_0000649 GCST90269797 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HEPE, Eicosanoid 9(S) HEPE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274319 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12(S) HEPE, Eicosanoid 15(S) HEPE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274320 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274321 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-HETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274322 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 10-Nitrooleate, Eicosanoid 9-Nitrooleate levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274323 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-EET, Eicosanoid 8,9-EET a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274324 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-EET, Eicosanoid 8,9-EET b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274325 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11(12)-EpETE, Eicosanoid 14(15) EpETE, Eicosanoid 15-oxoETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274326 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11(12)-EpETE, Eicosanoid 14(15) EpETE, Eicosanoid 15-oxoETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274327 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-diHETrE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274328 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-diHETrE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274329 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-HETE, Eicosanoid 12-HETE, Eicosanoid 8-HETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274330 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-2,3-dinor-TXB2 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274331 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-2,3-dinor-TXB2 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274332 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274333 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274334 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGE2, Eicosanoid 15k PGF2a, Eicosanoid PGD2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274335 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11d-TXB2 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274336 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11d-TXB2 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274337 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11t LTD4 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274338 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpEPE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274339 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274340 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274341 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274342 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 10,11-DiHDPA levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274227 Genome-wide genotyping array 2023-07-26 36804966 Zhang Q 2023-02-16 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/36804966 Identification of the BTN3A3 gene as a molecule implicated in generalized pustular psoriasis in a Chinese population. Generalized pustular psoriasis 161 Chinese Han ancestry cases, 364 Chinese Han ancestry controls 60 Chinese Han ancestry cases, 100 Chinese Han ancestry controls NR [431249] 2 psoriasis 14, pustular http://purl.obolibrary.org/obo/MONDO_0013626 GCST90274859 Exome-wide sequencing 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MMP-10 levels 961 individuals NA Illumina [11901634] (imputed) 2 matrix metalloproteinase 10 measurement http://www.ebi.ac.uk/efo/EFO_0010589 GCST90274904 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MMP-12 levels 961 individuals NA Illumina [11901634] (imputed) 12 matrix metalloproteinase 12 measurement http://www.ebi.ac.uk/efo/EFO_0010590 GCST90274905 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MMP-7 levels 961 individuals NA Illumina [11901634] (imputed) 2 matrix metalloproteinase 7 measurement http://www.ebi.ac.uk/efo/EFO_0010591 GCST90274906 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MPO levels 951 individuals NA Illumina [11901634] (imputed) 1 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90274907 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. NEMO levels 961 individuals NA Illumina [11901634] (imputed) 10 NF-kappa-B essential modulator measurement http://www.ebi.ac.uk/efo/EFO_0010597 GCST90274908 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. PECAM-1 levels 953 individuals NA Illumina [11901634] (imputed) 3 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90274909 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. RETN levels 961 individuals NA Illumina [11901634] (imputed) 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90274910 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. ST2 levels 961 individuals NA Illumina [11901634] (imputed) 5 ST2 protein measurement http://www.ebi.ac.uk/efo/EFO_0010599 GCST90274911 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. Stem cell factor levels 953 individuals NA Illumina [11901634] (imputed) 1 stem Cell Factor measurement http://www.ebi.ac.uk/efo/EFO_0008291 GCST90274912 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. TIE2 levels 953 individuals NA Illumina [11901634] (imputed) 3 angiopoietin-1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0010600 GCST90274913 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. TIM levels 959 individuals NA Illumina [11901634] (imputed) 2 hepatitis A virus cellular receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010601 GCST90274914 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. TM levels 961 individuals NA Illumina [11901634] (imputed) 1 thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0007774 GCST90274915 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. TRAIL levels 961 individuals NA Illumina [11901634] (imputed) 3 TNF-related apoptosis-inducing ligand measurement http://www.ebi.ac.uk/efo/EFO_0008300 GCST90274916 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. VEGFR-2 levels 953 individuals NA Illumina [11901634] (imputed) 2 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90274917 Genome-wide genotyping array 2023-06-26 36797040 Ortiz-Fernandez L 2023-02-16 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36797040 Identification of new risk loci shared across systemic vasculitides points towards potential target genes for drug repurposing. Vasculitis (pleiotropy) 8,467 European, Turkish, Asian or Middle Eastern ancestry cases, 29,795 European, Turkish, Asian or Middle Eastern ancestry controls NA NR [NR] (imputed) 14 vasculitis http://www.ebi.ac.uk/efo/EFO_0006803 GCST90271348 Genome-wide genotyping array 2023-06-29 36864135 Mathieson I 2023-03-02 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/36864135 Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Number of children ever born 785,604 European ancestry individuals 34,367 European ancestry women Affymetrix, Illumina [NR] (imputed) 5 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90271628 Genome-wide genotyping array 2023-06-29 36864135 Mathieson I 2023-03-02 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/36864135 Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Number of children ever born 306,980 European ancestry men NA Affymetrix, Illumina [NR] (imputed) 4 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90271629 Genome-wide genotyping array 2023-06-29 36864135 Mathieson I 2023-03-02 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/36864135 Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Number of children ever born 478,624 European ancestry women 34,367 European ancestry women Affymetrix, Illumina [NR] (imputed) 4 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90271630 Genome-wide genotyping array 2023-06-29 36864135 Mathieson I 2023-03-02 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/36864135 Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Lifetime childlessness 450,082 European ancestry individuals 34,367 European ancestry women Affymetrix [NR] (imputed) 3 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90271631 Genome-wide genotyping array 2023-06-29 36864135 Mathieson I 2023-03-02 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/36864135 Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Lifetime childlessness 205,035 European ancestry men NA Affymetrix [NR] (imputed) 4 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90271632 Genome-wide genotyping array 2023-06-29 36864135 Mathieson I 2023-03-02 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/36864135 Genome-wide analysis identifies genetic effects on reproductive success and ongoing natural selection at the FADS locus. Lifetime childlessness 245,047 European ancestry women 34,367 European ancestry women Affymetrix [NR] (imputed) 2 number of children ever born measurement http://www.ebi.ac.uk/efo/EFO_0009102 GCST90271633 Genome-wide genotyping array 2023-03-28 36194491 Hindy G 2022-10-04 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/36194491 Clinical, genetic, and experimental increase in soluble urokinase plasminogen activator receptor levels promotes atherosclerosis. Soluble urokinase plasminogen activator receptor levels 9,869 European ancestry individuals, 1,363 African American individuals, 623 Chinese American individuals, 1,082 Hispanic American individuals 12,177 European ancestry individuals NR [16600000] (imputed) 10 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90264159 Genome-wide genotyping array 2023-03-28 36194491 Hindy G 2022-10-04 J Clin Invest www.ncbi.nlm.nih.gov/pubmed/36194491 Clinical, genetic, and experimental increase in soluble urokinase plasminogen activator receptor levels promotes atherosclerosis. Soluble urokinase plasminogen activator receptor levels 9,869 European ancestry individuals 12,177 European ancestry individuals NR [9900000] (imputed) 9 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90264160 Genome-wide genotyping array 2023-04-19 37019578 Pirruccello JP 2023-04-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/37019578 The Genetic Determinants of Aortic Distention. Ascending aorta distensibility 32,639 European or unknown ancestry individuals NA Affymetrix [11617481] (imputed) 12 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90267385 Genome-wide genotyping array 2023-04-19 37019578 Pirruccello JP 2023-04-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/37019578 The Genetic Determinants of Aortic Distention. Descending aorta distensibility 33,907 European or unknown ancestry individuals NA Affymetrix [11619174] (imputed) 11 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90267386 Genome-wide genotyping array 2023-04-19 37019578 Pirruccello JP 2023-04-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/37019578 The Genetic Determinants of Aortic Distention. Central pulse pressure 37,672 European or unknown ancestry individuals NA Affymetrix [11619121] (imputed) 5 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90267387 Genome-wide genotyping array 2023-04-19 37019578 Pirruccello JP 2023-04-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/37019578 The Genetic Determinants of Aortic Distention. Ascending aorta strain 38,499 European or unknown ancestry individuals NA Affymetrix [11622183] (imputed) 26 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90267388 Genome-wide genotyping array 2023-04-19 37019578 Pirruccello JP 2023-04-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/37019578 The Genetic Determinants of Aortic Distention. Descending aorta strain 40,028 European or unknown ancestry individuals NA Affymetrix [11622901] (imputed) 21 aortic measurement http://www.ebi.ac.uk/efo/EFO_0020865 GCST90267389 Genome-wide genotyping array 2023-04-19 37019578 Pirruccello JP 2023-04-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/37019578 The Genetic Determinants of Aortic Distention. Ascending aorta diameter 38,372 European or unknown ancestry individuals NA Affymetrix [11622716] (imputed) 87 ascending aortic diameter http://www.ebi.ac.uk/efo/EFO_0021787 GCST90267390 Genome-wide genotyping array 2023-04-19 37019578 Pirruccello JP 2023-04-01 J Am Coll Cardiol www.ncbi.nlm.nih.gov/pubmed/37019578 The Genetic Determinants of Aortic Distention. Descending aorta diameter 39,893 European or unknown ancestry individuals NA Affymetrix [11622895] (imputed) 45 descending aortic diameter http://www.ebi.ac.uk/efo/EFO_0021788 GCST90267391 Genome-wide genotyping array 2023-06-28 36856146 Attaway AH 2023-03-01 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/36856146 Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. Sarcopenia in chronic obstructive pulmonary disease (fat-free mass index defined) 3,181 European ancestry cases, 29,245 European ancestry controls NA Affymetrix [NR] 3 sarcopenia http://www.ebi.ac.uk/efo/EFO_1000653 GCST90271634 Genome-wide genotyping array 2023-06-28 36856146 Attaway AH 2023-03-01 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/36856146 Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. Fat-free mass index in chronic obstructive pulmonary disease 32,426 European ancestry individuals 3,656 European ancestry individuals Affymetrix [NR] 1 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90271635 Genome-wide genotyping array 2023-06-28 36856146 Attaway AH 2023-03-01 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/36856146 Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. Appendicular skeletal muscle index in chronic obstructive pulmonary disease 32,426 European ancestry individuals NA Affymetrix [NR] 7 appendicular lean mass http://www.ebi.ac.uk/efo/EFO_0004980 GCST90271636 Genome-wide genotyping array 2023-06-28 36856146 Attaway AH 2023-03-01 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/36856146 Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. Hand grip strength in chronic obstructive pulmonary disease 32,426 European ancestry individuals NA Affymetrix [NR] 4 grip strength measurement http://www.ebi.ac.uk/efo/EFO_0006941 GCST90271637 Genome-wide genotyping array 2023-06-28 36856146 Attaway AH 2023-03-01 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/36856146 Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. Basal metabolic rate in chronic obstructive pulmonary disease 32,426 European ancestry individuals NA Affymetrix [NR] 7 base metabolic rate measurement http://www.ebi.ac.uk/efo/EFO_0007777 GCST90271638 Genome-wide genotyping array 2023-06-28 36856146 Attaway AH 2023-03-01 J Cachexia Sarcopenia Muscle www.ncbi.nlm.nih.gov/pubmed/36856146 Gene polymorphisms associated with heterogeneity and senescence characteristics of sarcopenia in chronic obstructive pulmonary disease. Sarcopenia in chronic obstructive pulmonary disease (fat-free mass index and hand-grip strength defined) 32,426 European ancestry individuals NA Affymetrix [NR] 3 sarcopenia http://www.ebi.ac.uk/efo/EFO_1000653 GCST90271639 Genome-wide genotyping array 2023-03-08 36581621 Huang J 2022-12-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36581621 Genomics and phenomics of body mass index reveals a complex disease network. Body mass index 1,122,049 European ancestry individuals NA Affymetrix [NR] (imputed) 2446 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90255621 Genome-wide genotyping array 2023-03-08 36581621 Huang J 2022-12-29 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36581621 Genomics and phenomics of body mass index reveals a complex disease network. Body mass index 42,752 African ancestry individuals, 55,525 African American individuals NA Affymetrix [NR] (imputed) 100 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90255622 Genome-wide genotyping array 2023-12-05 38018286 Toivonen J 2023-11-28 Vox Sang www.ncbi.nlm.nih.gov/pubmed/38018286 The value of genetic data from 665,460 individuals in managing iron deficiency anaemia and suitability to donate blood. Deferral due to hypohemoglobinemia in blood donors 6,714 Finnish (founder/genetic isolate) cases, 21,189 Finnish (founder/genetic isolate) controls NA Affymetrix [15956316] (imputed) 1 anemia http://purl.obolibrary.org/obo/MONDO_0002280 GCST90104113 Genome-wide genotyping array 2023-12-05 38018286 Toivonen J 2023-11-28 Vox Sang www.ncbi.nlm.nih.gov/pubmed/38018286 The value of genetic data from 665,460 individuals in managing iron deficiency anaemia and suitability to donate blood. Iron deficiency anaemia 18,076 Finnish or unknown ancestry cases, 647,384 Finnish or unknown ancestry controls NA Affymetrix [16700000] (imputed) 4 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90301371 Genome-wide genotyping array 2023-09-01 35848942 Degenhardt F 2022-11-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35848942 Detailed stratified GWAS analysis for severe COVID-19 in four European populations. COVID-19 with respiratory failure requiring mechanical ventilation 1,911 European ancestry cases, 12,226 European ancestry controls NA Illumina [9175283] (imputed) 10 respiratory failure, COVID-19 http://www.ebi.ac.uk/efo/EFO_0009686, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90278685 Genome-wide genotyping array 2023-09-01 35848942 Degenhardt F 2022-11-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35848942 Detailed stratified GWAS analysis for severe COVID-19 in four European populations. COVID-19 with respiratory failure requiring mechanical ventilation 6,526 European ancestry cases, 719,075 European ancestry controls, 6,526 NR ancestry cases, 719,075 NR ancestry controls NA Illumina [9309373] (imputed) 9 respiratory failure, COVID-19 http://www.ebi.ac.uk/efo/EFO_0009686, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90278686 Genome-wide genotyping array 2023-09-01 35848942 Degenhardt F 2022-11-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35848942 Detailed stratified GWAS analysis for severe COVID-19 in four European populations. COVID-19 with respiratory failure 3,255 European ancestry cases, 12,488 European ancestry controls NA Illumina [9223806] (imputed) 9 respiratory failure, COVID-19 http://www.ebi.ac.uk/efo/EFO_0009686, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90129579 Genome-wide genotyping array 2023-09-01 35848942 Degenhardt F 2022-11-01 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35848942 Detailed stratified GWAS analysis for severe COVID-19 in four European populations. COVID-19 with respiratory failure 14,467 European ancestry cases, 1,306,293 European ancestry controls, 14,467 NR ancestry cases, 1,306,293 NR ancestry controls NA Illumina [9163456] (imputed) 9 respiratory failure, COVID-19 http://www.ebi.ac.uk/efo/EFO_0009686, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90278684 Genome-wide genotyping array 2023-09-06 37120436 Granot-Hershkovitz E 2023-04-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37120436 Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment. Metabolomic risk score for mild cognitive impairment 3,890 Cuban, Central American, Dominican, Mexican, Puerto Rican, South American ancestry individuals 3,149 Cuban, Central American, Dominican, Mexican, Puerto Rican, South American ancestry individuals, 1,032 African American individuals, 3,775 European ancestry individuals NR [12518657] (imputed) 2 metabolite measurement, Cognitive impairment http://www.ebi.ac.uk/efo/EFO_0004725, http://purl.obolibrary.org/obo/HP_0100543 GCST90281110 Genome-wide genotyping array 2023-09-06 37120436 Granot-Hershkovitz E 2023-04-29 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37120436 Genetic loci of beta-aminoisobutyric acid are associated with aging-related mild cognitive impairment. Beta-aminoisobutyric acid levels 3,863 Cuban, Central American, Dominican, Mexican, Puerto Rican, South American ancestry individuals 3,149 Cuban, Central American, Dominican, Mexican, Puerto Rican, South American ancestry individuals, 1,032 African American individuals, 3,775 European ancestry individuals NR [12481432] (imputed) 8 beta-aminoisobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0010464 GCST90281111 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA1 volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 18 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267895 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA1 volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 13 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267894 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA3 volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 16 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267896 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA3 volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 9 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267897 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA4 volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 17 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267898 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield left CA4 volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 12 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267899 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left fimbria volume 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 5 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST90267900 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal left GC-ML-DG volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 13 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267901 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal left GC-ML-DG volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 13 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267902 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal left HATA volume 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 3 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST90267903 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 20 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267904 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (fissure) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 8 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267905 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 17 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267906 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (tail) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 24 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267907 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume 65,791 European ancestry, East Asian ancestry individuals NA NR [5048682] (imputed) 49 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267908 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left molecular layer hippocampal volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 9 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267909 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left molecular layer hippocampal volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 9 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267910 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left parasubiculum volume 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 3 parasubiculum volume http://www.ebi.ac.uk/efo/EFO_0009405 GCST90267911 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left presubiculum volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 11 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267912 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left presubiculum volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 6 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267913 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left subiculum volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 15 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267914 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left subiculum volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 9 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267915 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA1 volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 10 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267916 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA1 volume (head) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 15 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267917 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA3 volume (body) 38,977 European ancestry, East Asian ancestry individuals NA NR [5257171] (imputed) 11 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267918 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left fimbria volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST90267944 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal left GC-ML-DG volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267945 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal left GC-ML-DG volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 2 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267946 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal left HATA volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST90267947 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 2 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267948 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (fissure) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267949 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267950 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume (tail) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267951 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left hippocampal volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267952 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left molecular layer hippocampal volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 2 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267953 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left molecular layer hippocampal volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267954 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left parasubiculum volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 parasubiculum volume http://www.ebi.ac.uk/efo/EFO_0009405 GCST90267955 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left presubiculum volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267956 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left presubiculum volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267957 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left subiculum volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267958 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Left subiculum volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267959 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA1 volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267960 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA1 volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal CA1 volume http://www.ebi.ac.uk/efo/EFO_0009394 GCST90267961 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA3 volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267962 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA3 volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA3 volume http://www.ebi.ac.uk/efo/EFO_0009395 GCST90267963 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA4 volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267964 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal subfield right CA4 volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal CA4 volume http://www.ebi.ac.uk/efo/EFO_0009396 GCST90267965 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right fimbria volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampus fimbria volume http://www.ebi.ac.uk/efo/EFO_0009402 GCST90267966 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal right GC-ML-DG volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267967 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal right GC-ML-DG volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 dentate gyrus volume measurement http://www.ebi.ac.uk/efo/EFO_0010083 GCST90267968 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Hippocampal right HATA volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal amigdala transition area volume http://www.ebi.ac.uk/efo/EFO_0009401 GCST90267969 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 3 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267970 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (fissure) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267971 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267972 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume (tail) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267973 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right hippocampal volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90267974 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right molecular layer hippocampal volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 1 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267975 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right molecular layer hippocampal volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 hippocampus molecular layer volume http://www.ebi.ac.uk/efo/EFO_0009397 GCST90267976 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right parasubiculum volume 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 parasubiculum volume http://www.ebi.ac.uk/efo/EFO_0009405 GCST90267977 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right presubiculum volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267978 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right presubiculum volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 presubiculum volume http://www.ebi.ac.uk/efo/EFO_0009400 GCST90267979 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right subiculum volume (body) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 2 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267980 Genome-wide genotyping array 2023-06-28 37337106 Liu N 2023-06-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37337106 Cross-ancestry genome-wide association meta-analyses of hippocampal and subfield volumes. Right subiculum volume (head) 7,009 East Asian ancestry individuals NA NR [14105806] (imputed) 0 subiculum volume http://www.ebi.ac.uk/efo/EFO_0009399 GCST90267981 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder (ADuLT model adjusted for sex) 58,286 European ancestry individuals NA NR [8785478] (imputed) 12 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275136 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder (ADuLT model) 58,286 European ancestry individuals NA NR [8785478] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275137 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder (ADuLT model adjusted for age, sex) 58,286 European ancestry individuals NA NR [8785478] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275135 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism (ADuLT model adjusted for age, sex) 54,976 European ancestry individuals NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275138 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism (ADuLT model adjusted for sex) 54,976 European ancestry individuals NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275139 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism (ADuLT model) 54,976 European ancestry individuals NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275140 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression (ADuLT model adjusted for age, sex) 63,875 European ancestry individuals NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275141 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression (ADuLT model adjusted for sex) 63,875 European ancestry individuals NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275142 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression (ADuLT model) 63,875 European ancestry individuals NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275143 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia (ADuLT model adjusted for age, sex) 48,523 European ancestry individuals NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275144 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia (ADuLT model adjusted for sex) 48,523 European ancestry individuals NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275145 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia (ADuLT model) 48,523 European ancestry individuals NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275146 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder (adjusted for age, sex) 21,738 European ancestry cases, 36,548 European ancestry controls NA NR [8785478] (imputed) 1 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275147 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder (adjusted for sex) 21,738 European ancestry cases, 36,548 European ancestry controls NA NR [8785478] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275148 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder 21,738 European ancestry cases, 36,548 European ancestry controls NA NR [8785478] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275149 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism (adjusted for age, sex) 18,235 European ancestry cases, 36,741 European ancestry controls NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275150 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism (adjusted for sex) 18,235 European ancestry cases, 36,741 European ancestry controls NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275151 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism 18,235 European ancestry cases, 36,741 European ancestry controls NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275152 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression (adjusted for age, sex) 27,507 European ancestry cases, 36,368 European ancestry controls NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275153 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression (adjusted for sex) 27,507 European ancestry cases, 36,368 European ancestry controls NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275154 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression 27,507 European ancestry cases, 36,368 European ancestry controls NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275155 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia (adjusted for age, sex) 11,602 European ancestry cases, 36,921 European ancestry controls NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275156 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia (adjusted for sex) 11,602 European ancestry cases, 36,921 European ancestry controls NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275157 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia 11,602 European ancestry cases, 36,921 European ancestry controls NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275158 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder (SPACox model adjusted for age, sex) 21,738 European ancestry cases, 36,548 European ancestry controls NA NR [8785478] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275159 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Attention deficit hyperactivity disorder (SPACox model adjusted for sex) 21,738 European ancestry cases, 36,548 European ancestry controls NA NR [8785478] (imputed) 0 attention deficit hyperactivity disorder http://www.ebi.ac.uk/efo/EFO_0003888 GCST90275160 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism (SPACox model adjusted for age, sex) 18,235 European ancestry cases, 36,741 European ancestry controls NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275161 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Autism (SPACox model adjusted for sex) 18,235 European ancestry cases, 36,741 European ancestry controls NA NR [8785478] (imputed) 0 autism http://www.ebi.ac.uk/efo/EFO_0003758 GCST90275162 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression (SPACox model adjusted for age, sex) 27,507 European ancestry cases, 36,368 European ancestry controls NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275163 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Depression (SPACox model adjusted for sex) 27,507 European ancestry cases, 36,368 European ancestry controls NA NR [8785478] (imputed) 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90275164 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia (SPACox model adjusted for age, sex) 11,602 European ancestry cases, 36,921 European ancestry controls NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275165 Genome-wide genotyping array 2023-09-27 37689771 Pedersen EM 2023-09-09 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37689771 ADuLT: An efficient and robust time-to-event GWAS. Schizophrenia (SPACox model adjusted for sex) 11,602 European ancestry cases, 36,921 European ancestry controls NA NR [8785478] (imputed) 0 schizophrenia http://purl.obolibrary.org/obo/MONDO_0005090 GCST90275166 Genome-wide genotyping array 2023-09-05 37532928 McLaren PJ 2023-08-02 Nature www.ncbi.nlm.nih.gov/pubmed/37532928 Africa-specific human genetic variation near CHD1L associates with HIV-1 load. HIV setpoint viral load 3,879 African American or Afro-Caribbean, African ancestry individuals NA Affymetrix, Illumina [9600000] (imputed) 16 HIV viral set point measurement http://www.ebi.ac.uk/efo/EFO_0006319 GCST90269914 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Resistance to antihypertensive treatment in hypertension 12,132 cases, 19,857 controls NA Illumina [6318624] (imputed) 30 treatment-resistant hypertension http://www.ebi.ac.uk/efo/EFO_1002006 GCST90281355 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of anti-hypertensive diuretic in hypertension 5,153 cases, 1,016 controls NA Illumina [6276523] (imputed) 12 response to diuretic http://purl.obolibrary.org/obo/GO_0036270 GCST90281356 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of angiotensin II receptor blocker in hypertension 9,764 cases, 5,175 controls NA Illumina [6308025] (imputed) 26 response to angiotensin receptor blocker http://www.ebi.ac.uk/efo/EFO_0010735 GCST90281357 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of beta blocker in hypertension 3,336 cases, 1,060 controls NA Illumina [6265938] (imputed) 8 response to beta blocker http://www.ebi.ac.uk/efo/EFO_0007766 GCST90281358 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of angiotensin converting enzyme inhibitor in hypertension 3,977 cases, 1,284 controls NA Illumina [6268226] (imputed) 14 response to angiotensin-converting enzyme inhibitor http://www.ebi.ac.uk/efo/EFO_0005325 GCST90281359 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of alpha blocker in hypertension 2,670 cases, 223 controls NA Illumina [6205791] (imputed) 14 response to antihypertensive drug http://www.ebi.ac.uk/efo/EFO_0005405 GCST90281360 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of calcium channel blocker in hypertension 10,514 cases, 10,307 controls NA Illumina [6313938] (imputed) 21 response to calcium channel blocker http://www.ebi.ac.uk/efo/EFO_0007767 GCST90281361 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of alpha-beta blocker in hypertension 4,542 cases, 784 controls NA Illumina [6260676] (imputed) 11 response to antihypertensive drug http://www.ebi.ac.uk/efo/EFO_0005405 GCST90281362 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of calcium channel blocker-dihydropyridine in hypertension 10,206 cases, 8,411 controls NA Illumina [6302793] (imputed) 22 response to calcium channel blocker http://www.ebi.ac.uk/efo/EFO_0007767 GCST90281363 Genome-wide genotyping array 2023-09-21 37151119 Yamazaki K 2023-05-07 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/37151119 Genome-wide association studies categorized by class of anti-hypertensive drugs reveal complex pathogenesis of hypertension with drug resistance. Treatment effectiveness of calcium channel blocker-benzothiazepine in hypertension 902 cases, 1,383 controls NA Illumina [6261498] (imputed) 9 response to calcium channel blocker http://www.ebi.ac.uk/efo/EFO_0007767 GCST90281364 Genome-wide genotyping array 2023-11-09 35110524 Bjornsdottir G 2022-02-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35110524 Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. ICD10 M54: Dorsalgia 119,110 European ancestry cases, 909,847 European ancestry controls NA Affymetrix, Illumina [53500000] (imputed) 22 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90103484 Genome-wide genotyping array 2023-11-09 35110524 Bjornsdottir G 2022-02-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35110524 Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. Intervertebral disc disorder with herniated lumbar discs requiring surgery 9,188 European ancestry cases, 780,323 European ancestry controls NA Affymetrix, Illumina [53500000] (imputed) 3 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90103485 Genome-wide genotyping array 2023-11-09 35110524 Bjornsdottir G 2022-02-02 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35110524 Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology. ICD10 M51: Intervertebral disc disorder 58,854 European ancestry cases, 922,958 European ancestry controls NA Affymetrix, Illumina [53500000] (imputed) 27 Back pain http://purl.obolibrary.org/obo/HP_0003418 GCST90103483 Genome-wide genotyping array 2023-07-07 36889626 Zhang L 2023-03-06 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/36889626 A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses. Body mass index or osteoarthritis (pleiotropy) 806,834 European ancestry BMI individuals, 177,517 European ancestry osteoarthritis cases, 649,173 European ancestry controls NA NR [NR] 34 body mass index, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0004340, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90271767 Genome-wide genotyping array 2023-07-07 36889626 Zhang L 2023-03-06 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/36889626 A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses. Body mass index or osteoarthritis (pleiotropy) 374,756 European ancestry BMI males, 56,462 European ancestry osteoarthritis male cases, 153,808 European ancestry male controls NA NR [NR] 2 body mass index, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0004340, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90271768 Genome-wide genotyping array 2023-07-07 36889626 Zhang L 2023-03-06 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/36889626 A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses. Body mass index or osteoarthritis (pleiotropy) 434,794 European ancestry BMI females, 90,838 European ancestry osteoarthritis female cases, 192,697 European ancestry female controls NA NR [NR] 13 body mass index, osteoarthritis http://www.ebi.ac.uk/efo/EFO_0004340, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90271769 Genome-wide genotyping array 2023-07-07 36889626 Zhang L 2023-03-06 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/36889626 A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses. Body mass index or knee osteoarthritis (pleiotropy) 806,834 European ancestry BMI individuals, 62,497 European ancestry knee osteoarthritis cases, 333,557 European ancestry controls NA NR [NR] 28 osteoarthritis, knee, body mass index http://www.ebi.ac.uk/efo/EFO_0004616, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90271770 Genome-wide genotyping array 2023-07-07 36889626 Zhang L 2023-03-06 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/36889626 A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses. Body mass index or hip osteoarthritis (pleiotropy) 806,834 European ancestry BMI individuals, 36,445 European ancestry hip osteoarthritis cases, 316,943 European ancestry controls NA NR [NR] 22 osteoarthritis, hip, body mass index http://www.ebi.ac.uk/efo/EFO_1000786, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90271771 Genome-wide genotyping array 2023-07-07 36889626 Zhang L 2023-03-06 Osteoarthritis Cartilage www.ncbi.nlm.nih.gov/pubmed/36889626 A sex- and site-specific relationship between body mass index and osteoarthritis: evidence from observational and genetic analyses. Body mass index or spine osteoarthritis (pleiotropy) 806,834 European ancestry BMI individuals, 28,372 European ancestry spine osteoarthritis cases, 305,578 European ancestry controls NA NR [NR] 5 osteoarthritis, spine, body mass index http://www.ebi.ac.uk/efo/EFO_1000787, http://www.ebi.ac.uk/efo/EFO_0004340 GCST90271772 Genome-wide genotyping array 2023-09-07 36882501 Humphries EM 2023-03-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36882501 Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population. Mood disorder 1,672 Old Order Amish (founder/genetic isolate) ancestry individuals NA NR [6600000] (imputed) 4 mood disorder http://www.ebi.ac.uk/efo/EFO_0004247 GCST90281184 Genome-wide genotyping array, Genome-wide sequencing [Illumina] 2023-10-13 36651668 Webber D 2023-01-18 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/36651668 Genetics of Osteonecrosis in Children and Adults with Systemic Lupus Erythematosus. Time to osteonecrosis in systemic lupus erythematosus 305 European ancestry individuals, 240 East Asian ancestry individuals, 123 African ancestry individuals, 89 South Asian ancestry individuals, 25 Amerindian ancestry individuals, 158 admixed ancestry individuals NA Illumina [4431911] (imputed) 30 age at diagnosis, osteonecrosis http://www.ebi.ac.uk/efo/EFO_0004918, http://www.ebi.ac.uk/efo/EFO_0004259 GCST90295969 Genome-wide genotyping array 2023-10-13 36651668 Webber D 2023-01-18 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/36651668 Genetics of Osteonecrosis in Children and Adults with Systemic Lupus Erythematosus. Osteonecrosis in systemic lupus erythematosus 12 European ancestry cases, 293 European ancestry controls, 16 East Asian ancestry cases, 224 East Asian ancestry controls, 17 African ancestry cases, 106 African ancestry controls, 12 South Asian ancestry cases, 77 South Asian ancestry controls, 2 Amerindian ancestry cases, 23 Amerindian ancestry controls, 12 admixed ancestry cases, 146 admixed ancestry controls NA Illumina [NR] (imputed) 15 osteonecrosis http://www.ebi.ac.uk/efo/EFO_0004259 GCST90295970 Genome-wide genotyping array 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking initiation 119,589 African ancestry individuals NA NR [NR] (imputed) 0 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST90243965 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking initiation 286,026 Hispanic or Latin American individuals NA NR [NR] (imputed) 23 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST90243966 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking initiation 296,395 East Asian ancestry individuals NA NR [NR] (imputed) 7 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST90243967 Genome-wide genotyping array, Genome-wide sequencing 2022-12-21 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking initiation 2,669,029 European ancestry individuals NA NR [NR] (imputed) 1752 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST90243968 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Age of smoking initiation 17,508 African ancestry individuals NA NR [NR] (imputed) 0 age at initiation of smoking http://www.ebi.ac.uk/efo/EFO_0021784 GCST90243969 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Age of smoking initiation 33,914 Hispanic or Latin American individuals NA NR [NR] (imputed) 0 age at initiation of smoking http://www.ebi.ac.uk/efo/EFO_0021784 GCST90243970 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Age of smoking initiation 63,353 East Asian ancestry individuals NA NR [NR] (imputed) 0 age at initiation of smoking http://www.ebi.ac.uk/efo/EFO_0021784 GCST90243971 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Age of smoking initiation 618,541 European ancestry individuals NA NR [NR] (imputed) 26 age at initiation of smoking http://www.ebi.ac.uk/efo/EFO_0021784 GCST90243972 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Cigarettes smoked per day 20,157 African ancestry individuals NA NR [NR] (imputed) 2 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90243973 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Cigarettes smoked per day 35,129 Hispanic or Latin American individuals NA NR [NR] (imputed) 2 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90243974 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Cigarettes smoked per day 108,275 East Asian ancestry individuals NA NR [NR] (imputed) 16 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90243975 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Cigarettes smoked per day 618,489 European ancestry individuals NA NR [NR] (imputed) 153 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90243976 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking cessation 34,970 African ancestry individuals NA NR [NR] (imputed) 0 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST90243977 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking cessation 90,525 Hispanic or Latin American individuals NA NR [NR] (imputed) 0 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST90243978 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking cessation 160,775 East Asian ancestry individuals NA NR [NR] (imputed) 4 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST90243979 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking cessation 1,147,272 European ancestry individuals NA NR [NR] (imputed) 125 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST90243980 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Drinks per week 95,343 African ancestry individuals NA NR [NR] (imputed) 1 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90243981 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Drinks per week 274,707 Hispanic or Latin American individuals NA NR [NR] (imputed) 7 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90243982 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Drinks per week 121,859 East Asian ancestry individuals NA NR [NR] (imputed) 9 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90243983 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Drinks per week 2,428,851 European ancestry individuals NA NR [NR] (imputed) 501 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90243984 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking initiation 3,382,012 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals NA NR [NR] (imputed) 2486 smoking initiation http://www.ebi.ac.uk/efo/EFO_0005670 GCST90243985 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Age of smoking initiation 728,455 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals NA NR [NR] (imputed) 39 age at initiation of smoking http://www.ebi.ac.uk/efo/EFO_0021784 GCST90243986 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Cigarettes smoked per day 783,784 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals NA NR [NR] (imputed) 243 cigarettes per day measurement http://www.ebi.ac.uk/efo/EFO_0006525 GCST90243987 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Smoking cessation 1,400,535 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals NA NR [NR] (imputed) 206 smoking cessation http://www.ebi.ac.uk/efo/EFO_0004319 GCST90243988 Genome-wide genotyping array, Genome-wide sequencing 2022-12-14 36477530 Saunders GRB 2022-12-07 Nature www.ncbi.nlm.nih.gov/pubmed/36477530 Genetic diversity fuels gene discovery for tobacco and alcohol use. Drinks per week 2,965,643 European ancestry, East Asian ancestry, Hispanic or Latin American, African ancestry individuals NA NR [NR] (imputed) 849 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90243989 Genome-wide genotyping array, Genome-wide sequencing 2023-11-15 37296840 Nudelman K 2023-05-23 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/37296840 Genetic Variants Associated with Longitudinal Cognitive Performance in Older Breast Cancer Patients and Controls. Longitudinal cognitive performance (attention, processing and executive function) x breast cancer interaction 325 European ancestry older female survivor cases, 340 European ancestry older controls NA Affymetrix, Illumina [7661137] (imputed) 2 cognitive domain measurement, breast cancer http://www.ebi.ac.uk/efo/EFO_0009098, http://purl.obolibrary.org/obo/MONDO_0007254 GCST90297546 Genome-wide genotyping array 2023-11-15 37296840 Nudelman K 2023-05-23 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/37296840 Genetic Variants Associated with Longitudinal Cognitive Performance in Older Breast Cancer Patients and Controls. Longitudinal cognitive performance (learning and memory) x breast cancer interaction 325 European ancestry older female survivor cases, 340 European ancestry older controls NA Affymetrix, Illumina [7661137] (imputed) 0 cognitive domain measurement, breast cancer http://www.ebi.ac.uk/efo/EFO_0009098, http://purl.obolibrary.org/obo/MONDO_0007254 GCST90297547 Genome-wide genotyping array 2023-11-30 37232355 Fan J 2023-05-26 Mol Carcinog www.ncbi.nlm.nih.gov/pubmed/37232355 A two-stage genome-wide association study identified four potential early-onset nonsmall cell lung cancer risk loci based on 26,652 participants in Chinese population. Early onset non-small cell lung cancer 2,556 Chinese ancestry cases, 13,327 Chinese ancestry controls NA NR [NR] (imputed) 7 non-small cell lung carcinoma http://www.ebi.ac.uk/efo/EFO_0003060 GCST90301329 Genome-wide genotyping array 2023-11-16 37288313 Hsu WT 2023-05-24 Brain Commun www.ncbi.nlm.nih.gov/pubmed/37288313 Genome-phenome wide association study of broadly defined headache. Headache 12,026 Taiwanese Han Chinese ancestry cases, 96,829 Taiwanese Han Chinese ancestry controls NA Affymetrix [4230987] (imputed) 7 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90297550 Genome-wide genotyping array 2023-11-16 37288313 Hsu WT 2023-05-24 Brain Commun www.ncbi.nlm.nih.gov/pubmed/37288313 Genome-phenome wide association study of broadly defined headache. Severe headache 1,874 Taiwanese Han Chinese ancestry cases, 96,829 Taiwanese Han Chinese ancestry controls NA Affymetrix [4230987] (imputed) 31 Headache http://purl.obolibrary.org/obo/HP_0002315 GCST90297551 Genome-wide genotyping array 2023-11-15 37222225 Huang H 2023-05-24 Psychiatr Genet www.ncbi.nlm.nih.gov/pubmed/37222225 Genome-wide by environment interaction studies of maternal smoking and educational score in UK biobank. Educational score x maternal smoking during pregnancy interaction 85,362 British ancestry exposed offspring, 191,637 British ancestry unexposed offspring 12,028 British ancestry exposed offspring, 26,853 British ancestry unexposed offspring Affymetrix [NR] (imputed) 0 educational attainment, tobacco smoke exposure measurement http://www.ebi.ac.uk/efo/EFO_0011015, http://www.ebi.ac.uk/efo/EFO_0009115 GCST90297549 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hypertension 14,834 Korean ancestry cases, 57,395 Korean ancestry controls NA NR [8056211] (imputed) 28 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90255392 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Diabetes 5,083 Korean ancestry cases, 67,127 Korean ancestry controls NA NR [8056211] (imputed) 12 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90255393 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Thyroid disease 3,113 Korean ancestry cases, 64,004 Korean ancestry controls NA NR [8056211] (imputed) 5 thyroid disease http://www.ebi.ac.uk/efo/EFO_1000627 GCST90255394 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hyperlipidemia 7,099 Korean ancestry cases, 65,111 Korean ancestry controls NA NR [8056211] (imputed) 14 hyperlipidemia http://purl.obolibrary.org/obo/MONDO_0021187 GCST90255395 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Lung cancer 45 Korean ancestry cases, 72,253 Korean ancestry controls NA NR [8056211] (imputed) 0 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90255396 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Gastric cancer 378 Korean ancestry cases, 71,920 Korean ancestry controls NA NR [8056211] (imputed) 0 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90255397 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Liver cancer 46 Korean ancestry cases, 72,252 Korean ancestry controls NA NR [8056211] (imputed) 0 hepatocellular carcinoma http://www.ebi.ac.uk/efo/EFO_0000182 GCST90255398 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Colon cancer 240 Korean ancestry cases, 72,058 Korean ancestry controls NA NR [8056211] (imputed) 0 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90255399 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Pancreatic cancer 4 Korean ancestry cases, 72,294 Korean ancestry controls NA NR [8056211] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90255400 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Uterine cancer 355 Korean ancestry cases, 45,975 Korean ancestry controls NA NR [8056211] (imputed) 0 uterine carcinoma http://www.ebi.ac.uk/efo/EFO_0002919 GCST90255401 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Breast cancer 424 Korean ancestry cases, 45,906 Korean ancestry controls NA NR [8056211] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90255402 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Thyroid cancer 476 Korean ancestry cases, 71,822 Korean ancestry controls NA NR [8056211] (imputed) 0 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90255403 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Prostate cancer 44 Korean ancestry cases, 25,924 Korean ancestry controls NA NR [8056211] (imputed) 0 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90255404 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Gallbladder cancer 12 Korean ancestry cases, 72,286 Korean ancestry controls NA NR [8056211] (imputed) 0 gallbladder neoplasm http://www.ebi.ac.uk/efo/EFO_0004606 GCST90255405 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Systolic blood pressure 72,265 Korean ancestry individuals NA NR [8056211] (imputed) 24 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90255406 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Diastolic blood pressure 72,265 Korean ancestry individuals NA NR [8056211] (imputed) 29 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90255407 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Pulse rate 65,812 Korean ancestry individuals NA NR [8056211] (imputed) 19 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90255408 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Waist circumference 72,222 Korean ancestry individuals NA NR [8056211] (imputed) 19 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90255409 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hip circumference 72,157 Korean ancestry individuals NA NR [8056211] (imputed) 35 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90255410 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Height 72,288 Korean ancestry individuals NA NR [8056211] (imputed) 231 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90255411 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Weight 72,284 Korean ancestry individuals NA NR [8056211] (imputed) 55 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90255412 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. BMI 72,282 Korean ancestry individuals NA NR [8056211] (imputed) 37 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90255413 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hemoglobin A1c levels 38,288 Korean ancestry individuals NA NR [8056211] (imputed) 48 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90255414 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Glucose levels 70,698 Korean ancestry individuals NA NR [8056211] (imputed) 75 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90255415 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Blood urea nitrogen levels 72,286 Korean ancestry individuals NA NR [8056211] (imputed) 72 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST90255416 Genome-wide genotyping array 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Paired immunoglobulin-like type 2 receptor beta levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of paired immunoglobulin-like type 2 receptor beta in blood serum http://purl.obolibrary.org/obo/OBA_2044996 GCST90179391 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Perlecan levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of basement membrane-specific heparan sulfate proteoglycan core protein in blood serum http://purl.obolibrary.org/obo/OBA_2041954 GCST90179392 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Paraoxonase levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30602149] 4 level of serum paraoxonase/arylesterase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044998 GCST90179393 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Protein phosphatase inhibitor 2 levels 2,880 Greek (founder/geneitc isolate) individuals NA Illumina [30524494] 0 level of protein phosphatase inhibitor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043003 GCST90179394 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Prolargin levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 level of prolargin in blood serum http://purl.obolibrary.org/obo/OBA_2045000 GCST90179395 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Serine protease 27 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 4 serine protease 27 measurement http://www.ebi.ac.uk/efo/EFO_0008280 GCST90179396 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Prostasin levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 level of prostasin in blood serum http://purl.obolibrary.org/obo/OBA_2043048 GCST90179397 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Myeloblastin levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90179398 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. P-selectin glycoprotein ligand 1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 P-selectin glycoprotein ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0010922 GCST90179399 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Pulmonary surfactant-associated protein D levels 2,914 Greek (founder/geneitc isolate) individuals NA Illumina [30596778] 5 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90179400 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Pentraxin-related protein PTX3 levels 2,849 Greek (founder/geneitc isolate) individuals NA Illumina [30463540] 0 pentraxin-related protein PTX3 measurement http://www.ebi.ac.uk/efo/EFO_0010923 GCST90179401 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Dihydropteridine reductase levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of dihydropteridine reductase in blood serum http://purl.obolibrary.org/obo/OBA_2043129 GCST90179402 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Receptor for advanced glycosylation end products levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 level of advanced glycosylation end product-specific receptor in blood serum http://purl.obolibrary.org/obo/OBA_2045003 GCST90179403 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Retinoic acid receptor responder protein 2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 retinoic acid receptor responder protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008274 GCST90179404 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Regenerating islet-derived protein 4 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 regenerating islet-derived protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021921 GCST90179405 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Renin levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 renin measurement http://www.ebi.ac.uk/efo/EFO_0010616 GCST90179406 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Resistin levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90179407 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Eosinophil cationic protein levels 2,901 Greek (founder/geneitc isolate) individuals NA Illumina [30562907] 2 eosinophil cationic protein measurement http://www.ebi.ac.uk/efo/EFO_0010913 GCST90179408 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Inactive tyrosine-protein kinase transmembrane receptor ROR1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 tyrosine-protein kinase transmembrane receptor ROR1 measurement http://www.ebi.ac.uk/efo/EFO_0020831 GCST90179409 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Reticulon-4 receptor levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30565621] 2 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90179410 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Stem cell factor levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 stem Cell Factor measurement http://www.ebi.ac.uk/efo/EFO_0008291 GCST90179411 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Secretoglobin family 3A member 2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 level of secretoglobin family 3A member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2045004 GCST90179412 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Syndecan-4 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of syndecan-4 in blood serum http://purl.obolibrary.org/obo/OBA_2045005 GCST90179413 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. E-selectin levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90179414 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. P-selectin levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 4 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90179415 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Angiopoietin-1 receptor levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 4 angiopoietin-1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0010600 GCST90179441 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Metalloproteinase inhibitor 4 levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30603603] 2 level of metalloproteinase inhibitor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043856 GCST90179442 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tubulointerstitial nephritis antigen-like levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of tubulointerstitial nephritis antigen-like in blood serum http://purl.obolibrary.org/obo/OBA_2043857 GCST90179443 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Trem-like transcript 2 protein levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of trem-like transcript 2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043928 GCST90179444 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Thrombomodulin levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 thrombomodulin measurement http://www.ebi.ac.uk/efo/EFO_0007774 GCST90179445 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 tumor necrosis factor receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010931 GCST90179446 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor 2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 tumor necrosis factor receptor II measurement http://www.ebi.ac.uk/efo/EFO_0008384 GCST90179447 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor superfamily member 10A levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 tumor necrosis factor receptor superfamily member 10A measurement http://www.ebi.ac.uk/efo/EFO_0020799 GCST90179448 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor superfamily member 10C levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of tumor necrosis factor receptor superfamily member 10C in blood serum http://purl.obolibrary.org/obo/OBA_2045021 GCST90179449 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor superfamily member 11A levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 tumor necrosis factor receptor superfamily member 11A measurement http://www.ebi.ac.uk/efo/EFO_0020800 GCST90179450 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor superfamily member 13B levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 tumor necrosis factor receptor superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020803 GCST90179451 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor superfamily member 14 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 tumor necrosis factor receptor superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0020805 GCST90179452 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor ligand superfamily member 13B levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 tumor necrosis factor ligand superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020793 GCST90179453 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tissue-type plasminogen activator levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 tissue-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0020776 GCST90179454 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Transferrin receptor protein 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of transferrin receptor protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2045022 GCST90179455 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. TNF-related apoptosis-inducing ligand receptor 2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 TNF-related apoptosis-inducing ligand receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0010930 GCST90179456 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tartrate-resistant acid phosphatase type 5 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90179457 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Thyrotropin subunit beta levels 2,842 Greek (founder/geneitc isolate) individuals NA Illumina [30418954] 0 level of thyrotropin subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2045023 GCST90179458 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Thioredoxin domain-containing protein 5 levels 2,902 Greek (founder/geneitc isolate) individuals NA Illumina [30564778] 2 level of thioredoxin domain-containing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043969 GCST90179459 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Thymidine phosphorylase levels 2,896 Greek (founder/geneitc isolate) individuals NA Illumina [30546120] 2 level of thymidine phosphorylase in blood serum http://purl.obolibrary.org/obo/OBA_2043975 GCST90179460 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tyrosine-protein kinase receptor TYRO3 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 4 tyrosine-protein kinase receptor TYRO3 measurement http://www.ebi.ac.uk/efo/EFO_0020829 GCST90179461 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Urokinase-type plasminogen activator levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90179462 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Urokinase plasminogen activator surface receptor levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90179463 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Versican core protein levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of versican core protein in blood serum http://purl.obolibrary.org/obo/OBA_2044088 GCST90179464 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. vascular endothelial growth factor D levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90179465 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Semaphorin-3F levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of semaphorin-3F in blood serum http://purl.obolibrary.org/obo/OBA_2045006 GCST90179416 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Serpin A12 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 level of serpin A12 in blood serum http://purl.obolibrary.org/obo/OBA_2045007 GCST90179417 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Serpin B6 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of serpin B6 in blood serum http://purl.obolibrary.org/obo/OBA_2045008 GCST90179418 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Serpin B8 levels 2,828 Greek (founder/geneitc isolate) individuals NA Illumina [30298367] 2 level of serpin B8 in blood serum http://purl.obolibrary.org/obo/OBA_2043463 GCST90179419 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tyrosine-protein phosphatase non-receptor type substrate 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of tyrosine-protein phosphatase non-receptor type substrate 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040362 GCST90179420 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Sialic acid-binding Ig-like lectin 7 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 3 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90179421 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. SLAM family member 7 levels 2,856 Greek (founder/geneitc isolate) individuals NA Illumina [30454901] 1 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90179422 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Superoxide dismutase [Mn],mitochondrial levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 level of superoxide dismutase [Mn], mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043595 GCST90179423 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Sortilin levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 sortilin measurement http://www.ebi.ac.uk/efo/EFO_0600000 GCST90179424 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Sclerostin levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30565519] 1 sclerostin measurement http://www.ebi.ac.uk/efo/EFO_0010606 GCST90179425 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Spondin-1 levels 2,914 Greek (founder/geneitc isolate) individuals NA Illumina [30596141] 3 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90179426 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Spondin-2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 level of spondin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043641 GCST90179427 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Proto-oncogene tyrosine-protein kinase Src levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 proto-oncogene tyrosine-protein kinase Src measurement http://www.ebi.ac.uk/efo/EFO_0010927 GCST90179428 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Scavenger receptor cysteine-rich domain-containing group B protein levels 2,849 Greek (founder/geneitc isolate) individuals NA Illumina [30421387] 1 level of scavenger receptor cysteine-rich domain-containing group B protein in blood serum http://purl.obolibrary.org/obo/OBA_2045013 GCST90179429 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. ST2 protein levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 ST2 protein measurement http://www.ebi.ac.uk/efo/EFO_0010599 GCST90179430 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Serine/threonine-protein kinase 4 levels 2,571 Greek (founder/geneitc isolate) individuals NA Illumina [29864846] 0 level of serine/threonine-protein kinase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043700 GCST90179431 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Sulfatase-modifying factor 2 levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30565944] 3 level of inactive C-alpha-formylglycine-generating enzyme 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043733 GCST90179432 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tissue factor levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 tissue factor measurement http://www.ebi.ac.uk/efo/EFO_0010623 GCST90179433 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Trefoil factor 2 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 trefoil factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0021846 GCST90179434 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Trefoil factor 3 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90179435 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tissue factor pathway inhibitor levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90179436 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Protein-glutamine gamma-glutamyltransferase 2 levels 2,848 Greek (founder/geneitc isolate) individuals NA Illumina [30471590] 0 level of protein-glutamine gamma-glutamyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043839 GCST90179437 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Thrombospondin-2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90179438 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Thimet oligopeptidase levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30566212] 1 level of thimet oligopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2043843 GCST90179439 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Thrombopoietin levels 2,857 Greek (founder/geneitc isolate) individuals NA Illumina [30480933] 1 thrombopoietin measurement http://www.ebi.ac.uk/efo/EFO_0022004 GCST90179440 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. V-set and immunoglobulin domain-containing protein 2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 level of V-set and immunoglobulin domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044774 GCST90179466 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. von Willebrand factor levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 von Willebrand factor measurement http://www.ebi.ac.uk/efo/EFO_0004629 GCST90179467 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. X-C motif chemokine ligand 1 levels 2,837 Greek (founder/geneitc isolate) individuals NA Illumina [30453722] 3 level of lymphotactin in blood serum http://purl.obolibrary.org/obo/OBA_2045028 GCST90179468 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Angiotensin-converting enzyme 2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 angiotensin-converting enzyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0020150 GCST90179214 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Lysophosphatidic acid phosphatase type 6 levels 2,904 Greek (founder/geneitc isolate) individuals NA Illumina [30564716] 8 level of lysophosphatidic acid phosphatase type 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040483 GCST90179215 Genome-wide sequencing [HiSeqX] 2023-02-14 36536295 Vollenbrock CE 2022-12-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36536295 Genome-wide association study identifies novel loci associated with skin autofluorescence in individuals without diabetes. Skin autofluorescence 27,254 European ancestry individuals NA Illumina [9889051] (imputed) 5 advanced glycation end-product measurement http://www.ebi.ac.uk/efo/EFO_0007819 GCST90246326 Genome-wide genotyping array 2023-02-14 36536295 Vollenbrock CE 2022-12-19 BMC Genomics www.ncbi.nlm.nih.gov/pubmed/36536295 Genome-wide association study identifies novel loci associated with skin autofluorescence in individuals without diabetes. Skin reflectance 27,254 European ancestry individuals NA Illumina [9889051] (imputed) 27 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90246327 Genome-wide genotyping array 2022-12-05 32424261 Lee MJ 2020-05-18 Prostate Cancer Prostatic Dis www.ncbi.nlm.nih.gov/pubmed/32424261 Association between metformin medication, genetic variation and prostate cancer risk. Prostate cancer x metformin use interaction (simple model) 2,608 European ancestry individuals, 322 Asian ancestry individuals, 551 individuals NA Illumina [6504155] (imputed) 0 prostate carcinoma, response to metformin http://www.ebi.ac.uk/efo/EFO_0001663, http://purl.obolibrary.org/obo/GO_1901558 GCST90239844 Genome-wide genotyping array 2022-12-05 32424261 Lee MJ 2020-05-18 Prostate Cancer Prostatic Dis www.ncbi.nlm.nih.gov/pubmed/32424261 Association between metformin medication, genetic variation and prostate cancer risk. Prostate cancer x metformin use interaction (complex model) 2,608 European ancestry individuals, 322 Asian ancestry individuals, 551 individuals NA Illumina [6504155] (imputed) 1 prostate carcinoma, response to metformin http://www.ebi.ac.uk/efo/EFO_0001663, http://purl.obolibrary.org/obo/GO_1901558 GCST90239845 Genome-wide genotyping array 2022-12-05 32424261 Lee MJ 2020-05-18 Prostate Cancer Prostatic Dis www.ncbi.nlm.nih.gov/pubmed/32424261 Association between metformin medication, genetic variation and prostate cancer risk. High grade prostate cancer x metformin use interaction (simple model) 2,608 European ancestry individuals, 322 Asian ancestry individuals, 551 individuals NA Illumina [6504155] (imputed) 1 prostate carcinoma, response to metformin http://www.ebi.ac.uk/efo/EFO_0001663, http://purl.obolibrary.org/obo/GO_1901558 GCST90239846 Genome-wide genotyping array 2022-12-05 32424261 Lee MJ 2020-05-18 Prostate Cancer Prostatic Dis www.ncbi.nlm.nih.gov/pubmed/32424261 Association between metformin medication, genetic variation and prostate cancer risk. High grade prostate cancer x metformin use interaction (complex model) 2,608 European ancestry individuals, 322 Asian ancestry individuals, 551 individuals NA Illumina [6504155] (imputed) 0 prostate carcinoma, response to metformin http://www.ebi.ac.uk/efo/EFO_0001663, http://purl.obolibrary.org/obo/GO_1901558 GCST90239847 Genome-wide genotyping array 2023-08-21 37085903 Alemany S 2023-04-21 J Transl Med www.ncbi.nlm.nih.gov/pubmed/37085903 Genome-wide multi-trait analysis of irritable bowel syndrome and related mental conditions identifies 38 new independent variants. Irritable bowel syndrome (MTAG) 887,490 European ancestry individuals (MTAG effective sample size boosted by neuroticism, depression and anxiety samples) NA NR [NR] 42 irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0000555 GCST90277988 Genome-wide genotyping array 2023-08-18 36869385 Wang H 2023-03-03 Genome Med www.ncbi.nlm.nih.gov/pubmed/36869385 Identification of specific susceptibility loci for the early-onset colorectal cancer. Early onset colorectal cancer 1,490 European ancestry cases less than 50 years old, 19,951 European ancestry controls NA NR [2446560] (imputed) 4 colorectal cancer http://purl.obolibrary.org/obo/MONDO_0005575 GCST90271715 Genome-wide genotyping array 2023-08-18 36869385 Wang H 2023-03-03 Genome Med www.ncbi.nlm.nih.gov/pubmed/36869385 Identification of specific susceptibility loci for the early-onset colorectal cancer. Colorectal cancer (age of onset) 17,789 European ancestry cases NA NR [2446560] (imputed) 6 age of onset of colorectal cancer http://purl.obolibrary.org/obo/OBA_2050327 GCST90271716 Genome-wide genotyping array 2023-01-13 36292186 An HJ 2022-10-15 Diagnostics (Basel) www.ncbi.nlm.nih.gov/pubmed/36292186 Genome-Wide Association Study Identifies Genetic Variants Associated with Rotator Cuff Tear-A Pilot Study. Rotator cuff tears 20 East Asian ancestry cases, 20 East Asian ancestry controls NA Illumina [284246] 3 rotator cuff tear http://www.ebi.ac.uk/efo/EFO_1001250 GCST90244664 Exome-wide sequencing 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Metopion position ratio) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277920 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Metopion eminence depth) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277921 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Intercanthal width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277922 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Outercanthal width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277923 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right palpebral fissure height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277924 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left palpebral fissure height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277925 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right palpebrale fissure length) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277926 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left palpebrale fissure length) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277927 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eye angle of ex-ps) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277928 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eye angle of ex-ps) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277929 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eye angle of en-ps) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277930 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eye angle of en-ps) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277931 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eye angle of en-ps-ex) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277932 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eye angle of en-ps-ex) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277933 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Eye tail length) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277934 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Eye ratio of width to height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277935 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Ratio of eye width to base width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277936 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Subnasal width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277937 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Frontal nasal height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277938 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Profile nasal length) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277939 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Nasal bridge height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277940 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Nasal tip height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277941 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277952 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Nasal bridge depth) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277942 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Nasal tip protrusion) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277943 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Facial base width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277895 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Lower facial width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277896 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Upper facial width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277897 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Middle facial width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277898 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Upper lip height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277899 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Facial height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277900 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Upper facial area) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277901 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Lower facial area) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277902 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Facial width ratio of base to chin) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277903 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Facial ratio of base width to height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277904 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Facial ratio of chin width to height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277905 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right facial angle of en-ex-go) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 1 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277906 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left facial angle of en-ex-go) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277907 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right facial angle of ps-ex-go) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277908 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left facial angle of ps-ex-go) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277909 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right facial angle of en-ps-go) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277910 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left facial angle of en-ps-go) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277911 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Forehead height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277912 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Lower forehead height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277913 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Upper forehead height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277914 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Brow ridge height) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277915 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Upper forehead slant angle) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277916 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Brow ridge protrusion angle) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277917 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Upper forehead slant depth) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277918 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Brow ridge protrusion) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277919 Genome-wide genotyping array 2023-01-05 36578646 Yeh KH 2022-01-31 Tzu Chi Med J www.ncbi.nlm.nih.gov/pubmed/36578646 Circulating serum amyloid A levels but not SAA1 variants predict long-term outcomes of angiographically confirmed coronary artery disease. Amyloid A serum levels 2,199 East Asian ancestry individuals NA Affymetrix [614821] 2 serum amyloid A protein measurement http://www.ebi.ac.uk/efo/EFO_0004728 GCST90244128 Genome-wide genotyping array 2023-01-12 36220816 Selvaraj MS 2022-10-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36220816 Whole genome sequence analysis of blood lipid levels in >66,000 individuals. Low density lipoprotein cholesterol levels 29,502 European ancestry individuals, 16,983 Black individuals, 13,943 Hispanic individuals, 4,719 Asian ancestry individuals, 1,182 Samoan ancestry individuals 387,629 European ancestry individuals, 10,139 Black individuals, 500 Asian ancestry individuals, 96 South Asian ancestry individuals, 59 East Asian ancestry individuals, 71,748 individuals NR [428000000] 8 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90244653 Genome-wide sequencing 2023-01-12 36220816 Selvaraj MS 2022-10-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36220816 Whole genome sequence analysis of blood lipid levels in >66,000 individuals. High density lipoprotein cholesterol levels 29,502 European ancestry individuals, 16,983 Black individuals, 13,943 Hispanic individuals, 4,719 Asian ancestry individuals, 1,182 Samoan ancestry individuals 387,629 European ancestry individuals, 10,139 Black individuals, 500 Asian ancestry individuals, 96 South Asian ancestry individuals, 59 East Asian ancestry individuals, 71,748 individuals NR [428000000] 14 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90244654 Genome-wide sequencing 2023-01-12 36220816 Selvaraj MS 2022-10-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36220816 Whole genome sequence analysis of blood lipid levels in >66,000 individuals. Total cholesterol levels 29,502 European ancestry individuals, 16,983 Black individuals, 13,943 Hispanic individuals, 4,719 Asian ancestry individuals, 1,182 Samoan ancestry individuals 387,629 European ancestry individuals, 10,139 Black individuals, 500 Asian ancestry individuals, 96 South Asian ancestry individuals, 59 East Asian ancestry individuals, 71,748 individuals NR [428000000] 14 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90244655 Genome-wide sequencing 2023-01-12 36220816 Selvaraj MS 2022-10-11 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36220816 Whole genome sequence analysis of blood lipid levels in >66,000 individuals. Triglyceride levels 29,502 European ancestry individuals, 16,983 Black individuals, 13,943 Hispanic individuals, 4,719 Asian ancestry individuals, 1,182 Samoan ancestry individuals 387,629 European ancestry individuals, 10,139 Black individuals, 500 Asian ancestry individuals, 96 South Asian ancestry individuals, 59 East Asian ancestry individuals, 71,748 individuals NR [428000000] 5 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90244656 Genome-wide sequencing 2022-11-24 35213696 Ibanez L 2022-02-25 Brain www.ncbi.nlm.nih.gov/pubmed/35213696 Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke. Early neurological instability after acute ischemic stroke 5,063 European ancestry individuals NA Illumina [NR] (imputed) 4 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST90239734 Genome-wide genotyping array 2022-11-24 35213696 Ibanez L 2022-02-25 Brain www.ncbi.nlm.nih.gov/pubmed/35213696 Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke. Early neurological instability after acute ischemic stroke 324 African American individuals NA Illumina [NR] (imputed) 4 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST90239735 Genome-wide genotyping array 2022-11-24 35213696 Ibanez L 2022-02-25 Brain www.ncbi.nlm.nih.gov/pubmed/35213696 Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke. Early neurological instability after acute ischemic stroke 204 Hispanic individuals NA Illumina [NR] (imputed) 6 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST90239736 Genome-wide genotyping array 2022-11-24 35213696 Ibanez L 2022-02-25 Brain www.ncbi.nlm.nih.gov/pubmed/35213696 Multi-ancestry GWAS reveals excitotoxicity associated with outcome after ischaemic stroke. Early neurological instability after acute ischemic stroke 285 East Asian ancestry individuals NA Illumina [NR] (imputed) 2 stroke outcome severity measurement http://www.ebi.ac.uk/efo/EFO_0009603 GCST90239737 Genome-wide genotyping array 2023-01-18 36305391 Calabro M 2022-10-26 Pharmacogenet Genomics www.ncbi.nlm.nih.gov/pubmed/36305391 Body weight changes and bipolar disorder: a molecular pathway analysis. Weight change during bipolar disorder 568 European ancestry individuals, 16 Pacific Islander ancestry individuals, 21 African American individuals, 8 individuals, 6 Native American ancestry individuals NA NR [135804] 0 bipolar disorder, body weight http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0004338 GCST90244683 Genome-wide genotyping array 2023-02-13 36502284 Yu XH 2022-12-10 Obesity (Silver Spring) www.ncbi.nlm.nih.gov/pubmed/36502284 Body surface area is a potential obesity index: Its genetic determination and its causality for later-life diseases. Body surface area 337,198 British ancestry individuals NA NR [9428408] (imputed) 456 body surface area http://www.ebi.ac.uk/efo/EFO_0022196 GCST90245995 Genome-wide genotyping array 2023-01-18 36253440 Li QS 2022-10-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36253440 Genome-wide association study meta-analysis of suicide death and suicidal behavior. Suicide 3,765 European ancestry cases, 6,572 European ancestry controls NA Illumina [NR] (imputed) 13 suicide http://www.ebi.ac.uk/efo/EFO_0007624 GCST90244688 Genome-wide genotyping array 2023-01-18 36253440 Li QS 2022-10-17 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36253440 Genome-wide association study meta-analysis of suicide death and suicidal behavior. Suicide behavior 8,315 European ancestry cases, 256,478 European ancestry controls NA Illumina [NR] (imputed) 59 suicide behaviour http://www.ebi.ac.uk/efo/EFO_0007623 GCST90244689 Genome-wide genotyping array 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Junctional adhesion molecule A levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 level of junctional adhesion molecule A in blood serum http://purl.obolibrary.org/obo/OBA_2040343 GCST90179341 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Kidney Injury Molecule levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 kidney injury molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010917 GCST90179342 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Kallikrein-10 levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30565519] 3 level of kallikrein-10 in blood serum http://purl.obolibrary.org/obo/OBA_2042126 GCST90179343 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Kallikrein-6 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 kallikrein‐6 measurement http://www.ebi.ac.uk/efo/EFO_0010622 GCST90179344 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Kynurenine-oxoglutarate transaminase 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of kynurenine--oxoglutarate transaminase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040924 GCST90179345 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Low-density lipoprotein receptor levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 low-density lipoprotein receptor measurement http://www.ebi.ac.uk/efo/EFO_0021937 GCST90179346 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Leptin levels 2,856 Greek (founder/geneitc isolate) individuals NA Illumina [30479572] 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90179347 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Leukocyte immunoglobulin-like receptor subfamily A member 5 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 2 level of leukocyte immunoglobulin-like receptor subfamily A member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042197 GCST90179348 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Lectin-like oxidized LDL receptor 1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 lectin-like oxidized LDL receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010918 GCST90179349 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Lipoprotein lipase levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 level of lipoprotein lipase in blood serum http://purl.obolibrary.org/obo/OBA_2042223 GCST90179350 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Leucine-rich repeats and immunoglobulin-like domains protein 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 2 level of leucine-rich repeats and immunoglobulin-like domains protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042226 GCST90179351 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Low-density lipoprotein receptor-related protein 11 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 3 level of low-density lipoprotein receptor-related protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042229 GCST90179352 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Lymphotoxin-beta receptor levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of tumor necrosis factor receptor superfamily member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044979 GCST90179353 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Macrophage receptor MARCO levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 level of macrophage receptor MARCO in blood serum http://purl.obolibrary.org/obo/OBA_2040348 GCST90179354 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Myoglobin levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30601636] 0 myoglobin measurement http://www.ebi.ac.uk/efo/EFO_0005057 GCST90179355 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Multiple coagulation factor deficiency protein 2 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of multiple coagulation factor deficiency protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044981 GCST90179356 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Monocyte chemoattractant protein-1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of C-C motif chemokine 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044982 GCST90179357 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Meprin A subunit beta levels 2,560 Greek (founder/geneitc isolate) individuals NA Illumina [29987541] 3 level of meprin A subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2044983 GCST90179358 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Matrix extracellular phosphoglycoprotein levels 2,574 Greek (founder/geneitc isolate) individuals NA Illumina [29458620] 2 matrix extracellular phosphoglycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020557 GCST90179359 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tyrosine-protein kinase Mer levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 level of tyrosine-protein kinase Mer in blood serum http://purl.obolibrary.org/obo/OBA_2042340 GCST90179360 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Meteorin-like protein levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of meteorin-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042343 GCST90179361 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Matrix metalloproteinase-12 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 matrix metalloproteinase 12 measurement http://www.ebi.ac.uk/efo/EFO_0010590 GCST90179362 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Matrix metalloproteinase-2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of 72 kDa type IV collagenase in blood serum http://purl.obolibrary.org/obo/OBA_2044986 GCST90179363 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Matrix metalloproteinase-3 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of stromelysin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042390 GCST90179364 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Matrix metalloproteinase-7 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 matrix metalloproteinase 7 measurement http://www.ebi.ac.uk/efo/EFO_0010591 GCST90179365 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Coiled-coil domain-containing protein 80 levels 2,902 Greek (founder/geneitc isolate) individuals NA Illumina [30554553] 1 coiled-coil domain-containing protein 80 measurement http://www.ebi.ac.uk/efo/EFO_0020268 GCST90179241 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-C motif chemokine 15 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90179242 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-C motif chemokine 16 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90179243 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-C motif chemokine 17 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 8 C-C motif chemokine 17 measurement http://www.ebi.ac.uk/efo/EFO_0008045 GCST90179244 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-C motif chemokine 24 levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30603612] 2 C-C motif chemokine 24 measurement http://www.ebi.ac.uk/efo/EFO_0020197 GCST90179245 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-C motif chemokine 3 levels 2,845 Greek (founder/geneitc isolate) individuals NA Illumina [30423643] 3 C-C motif chemokine 3 measurement http://www.ebi.ac.uk/efo/EFO_0008051 GCST90179246 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Scavenger receptor cysteine-rich type 1 protein M130 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 scavenger receptor cysteine-rich type 1 protein m130 measurement http://www.ebi.ac.uk/efo/EFO_0020717 GCST90179247 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Sialomucin core protein 24 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 2 level of sialomucin core protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2044935 GCST90179248 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. T-cell surface glycoprotein CD1c levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of T-cell surface glycoprotein CD1c in blood serum http://purl.obolibrary.org/obo/OBA_2044936 GCST90179249 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. CD2-associated protein levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of CD2-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2040941 GCST90179250 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. T-cell surface glycoprotein CD4 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 t-cell surface glycoprotein CD4 measurement http://www.ebi.ac.uk/efo/EFO_0020760 GCST90179251 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. CD40 ligand levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 CD40 ligand measurement http://www.ebi.ac.uk/efo/EFO_0004790 GCST90179252 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. B-cell antigen receptor complex-associated protein beta chain levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of B-cell antigen receptor complex-associated protein beta chain in blood serum http://purl.obolibrary.org/obo/OBA_2040258 GCST90179253 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. SLAM family member 5 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90179254 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Complement component C1q receptor levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 6 level of complement component C1q receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040369 GCST90179255 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cadherin-2 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 cadherin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020212 GCST90179256 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cadherin-5 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 cadherin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008060 GCST90179257 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cadherin-related family member 5 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 3 level of cadherin-related family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042462 GCST90179258 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Carcinoembryonic antigenrelated cell adhesion molecule 8 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 level of carcinoembryonic antigen-related cell adhesion molecule 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040268 GCST90179259 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Chitinase-3-like protein 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 level of chitinase-3-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041005 GCST90179260 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Chitotriosidase-1 levels 2,701 Greek (founder/geneitc isolate) individuals NA Illumina [30129534] 2 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90179261 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Chordin-like protein 2 levels 2,872 Greek (founder/geneitc isolate) individuals NA Illumina [30483765] 2 level of chordin-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041016 GCST90179262 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-type lectin domain family 5 member A levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of C-type lectin domain family 5 member A in blood serum http://purl.obolibrary.org/obo/OBA_2044944 GCST90179263 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. CXADR-like membrane protein levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of adipocyte adhesion molecule in blood serum http://purl.obolibrary.org/obo/OBA_2044945 GCST90179264 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Calsyntenin-2 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 3 level of calsyntenin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041057 GCST90179265 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Matrix metalloproteinase-9 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 matrix metalloproteinase-9 measurement http://www.ebi.ac.uk/efo/EFO_0020561 GCST90179366 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Myeloperoxidase levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30603262] 1 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90179367 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. NAD kinase levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of NAD kinase in blood serum http://purl.obolibrary.org/obo/OBA_2042498 GCST90179368 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Nectin-2 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 2 level of nectin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040385 GCST90179369 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. NF-kappa-B essential modulator levels 2,855 Greek (founder/geneitc isolate) individuals NA Illumina [30476169] 0 NF-kappa-B essential modulator measurement http://www.ebi.ac.uk/efo/EFO_0010597 GCST90179370 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Nodal modulator 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 2 level of nodal modulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044990 GCST90179371 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Neurogenic locus notch homolog protein 3 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 neurogenic locus notch homolog protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020600 GCST90179372 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Neural proliferation differentiation and control protein 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of neural proliferation differentiation and control protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042612 GCST90179373 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Neuronal pentraxin receptor levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 2 level of neuronal pentraxin receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042624 GCST90179374 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Osteoprotegerin levels 2,843 Greek (founder/geneitc isolate) individuals NA Illumina [30420757] 1 osteoprotegerin measurement http://www.ebi.ac.uk/efo/EFO_0005918 GCST90179375 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Osteopontin levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30602965] 0 osteopontin measurement http://www.ebi.ac.uk/efo/EFO_0021776 GCST90179376 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Phosphoprotein associated with glycosphingolipid-enriched microdomains 1 levels 2,899 Greek (founder/geneitc isolate) individuals NA Illumina [30555986] 0 level of phosphoprotein associated with glycosphingolipid-enriched microdomains 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044993 GCST90179377 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Plasminogen activator inhibitor 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90179378 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Pappalysin-1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 pappalysin‐1 measurement http://www.ebi.ac.uk/efo/EFO_0010618 GCST90179379 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Proteinase-activated receptor 1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 proteinase-activated receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0010926 GCST90179380 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Poly [ADP-ribose] polymerase 1 levels 2,296 Greek (founder/geneitc isolate) individuals NA Illumina [28657944] 0 level of poly [ADP-ribose] polymerase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044994 GCST90179381 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Proprotein convertase subtilisin/kexin type 9 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90179382 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Platelet-derived growth factor subunit A levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of platelet-derived growth factor subunit A in blood serum http://purl.obolibrary.org/obo/OBA_2042824 GCST90179383 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Platelet-derived growth factor subunit B levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 platelet-derived growth factor subunit b measurement http://www.ebi.ac.uk/efo/EFO_0020650 GCST90179384 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Programmed cell death 1 ligand 2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 4 programmed cell death 1 ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0008268 GCST90179385 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Platelet endothelial cell adhesion molecule levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90179386 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Placenta growth factor levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 placenta growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010626 GCST90179387 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Peptidoglycan recognition protein 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90179388 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Elafin levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30602965] 1 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90179389 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Polymeric immunoglobulin receptor levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90179390 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. A disintegrin and metalloproteinase with thrombospondin motifs 13 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90179216 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Adhesion G protein-coupled receptor E2 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 adhesion G protein-coupled receptor E2 measurement http://www.ebi.ac.uk/efo/EFO_0021892 GCST90179217 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Adhesion G-protein coupled receptor G2 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of adhesion G-protein coupled receptor G2 in blood serum http://purl.obolibrary.org/obo/OBA_2041776 GCST90179218 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Agouti-related protein levels 2,857 Greek (founder/geneitc isolate) individuals NA Illumina [30481047] 1 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90179219 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. CD166 antigen levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 CD166 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020245 GCST90179220 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Retinal dehydrogenase 1 levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30566104] 0 level of aldehyde dehydrogenase 1A1 in blood serum http://purl.obolibrary.org/obo/OBA_2040558 GCST90179221 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Protein AMBP levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 level of protein AMBP in blood serum http://purl.obolibrary.org/obo/OBA_2040579 GCST90179222 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Angiopoietin-1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [18718848] 0 angiopoietin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020146 GCST90179223 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Angiopoietin-2 levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30560625] 0 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90179224 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Angiopoietin-related protein 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 2 level of angiopoietin-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044925 GCST90179225 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Angiopoietin-related protein 7 levels 2,899 Greek (founder/geneitc isolate) individuals NA Illumina [30561534] 1 level of angiopoietin-related protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040589 GCST90179226 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. DNA-(apurinic or apyrimidinic site) lyase levels 2,301 Greek (founder/geneitc isolate) individuals NA Illumina [29603609] 1 level of DNA-(apurinic or apyrimidinic site) endonuclease in blood serum http://purl.obolibrary.org/obo/OBA_2044927 GCST90179227 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Amyloid-like protein 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of amyloid beta precursor like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040617 GCST90179228 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Aminopeptidase N levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of aminopeptidase N in blood serum http://purl.obolibrary.org/obo/OBA_2044929 GCST90179229 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Arginase-1 levels 2,389 Greek (founder/geneitc isolate) individuals NA Illumina [29510260] 0 arginase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020160 GCST90179230 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tyrosine-protein kinase receptor UFO levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of tyrosine-protein kinase receptor UFO in blood serum http://purl.obolibrary.org/obo/OBA_2044930 GCST90179231 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Azurocidin levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 azurocidin measurement http://www.ebi.ac.uk/efo/EFO_0020170 GCST90179232 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Large proline-rich protein BAG6 levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30560984] 0 level of large proline-rich protein BAT3 in blood serum http://purl.obolibrary.org/obo/OBA_2040780 GCST90179233 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Bleomycin hydrolase levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of bleomycin hydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2040803 GCST90179234 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Bone morphogenetic protein 6 levels 2,771 Greek (founder/geneitc isolate) individuals NA Illumina [30279878] 3 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90179235 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Brother of CDO levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 brother of CDO measurement http://www.ebi.ac.uk/efo/EFO_0020194 GCST90179236 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Carbonic anhydrase 13 levels 2,827 Greek (founder/geneitc isolate) individuals NA Illumina [30423952] 0 carbonic anhydrase 13 measurement http://www.ebi.ac.uk/efo/EFO_0008067 GCST90179237 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Carbonic anhydrase 5A,mitochondrial levels 2,730 Greek (founder/geneitc isolate) individuals NA Illumina [30297343] 1 level of carbonic anhydrase 5A, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040859 GCST90179238 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Soluble calcium-activated nucleotidase 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of soluble calcium-activated nucleotidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040886 GCST90179239 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Caspase-3 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 caspase-3 measurement http://www.ebi.ac.uk/efo/EFO_0008070 GCST90179240 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Clusterin-like protein 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 6 level of clusterin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041061 GCST90179266 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Contactin-1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 contactin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020286 GCST90179267 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Collagen alpha-1 (I) chain levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 level of collagen alpha-1(I) chain in blood serum http://purl.obolibrary.org/obo/OBA_2044948 GCST90179268 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Carboxypeptidase A1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of carboxypeptidase A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041112 GCST90179269 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Carboxypeptidase B levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 level of carboxypeptidase B in blood serum http://purl.obolibrary.org/obo/OBA_2041115 GCST90179270 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Crk-like protein levels 2,466 Greek (founder/geneitc isolate) individuals NA Illumina [29695798] 0 level of Crk-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2041146 GCST90179271 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cystatin-B levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 cystatin B measurement http://www.ebi.ac.uk/efo/EFO_0010593 GCST90179272 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Chymotrypsin C levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 level of chymotrypsin-C in blood serum http://purl.obolibrary.org/obo/OBA_2041193 GCST90179273 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cathepsin D levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 cathepsin D measurement http://www.ebi.ac.uk/efo/EFO_0010611 GCST90179274 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Pro-cathepsin H levels 2,769 Greek (founder/geneitc isolate) individuals NA Illumina [30395066] 2 level of cathepsin H in blood serum http://purl.obolibrary.org/obo/OBA_2044953 GCST90179275 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cathepsin L1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 cathepsin L1 measurement http://www.ebi.ac.uk/efo/EFO_0010619 GCST90179276 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cathepsin O levels 2,904 Greek (founder/geneitc isolate) individuals NA Illumina [30564562] 2 level of cathepsin O in blood serum http://purl.obolibrary.org/obo/OBA_2041195 GCST90179277 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Cathepsin Z levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 cathepsin Z measurement http://www.ebi.ac.uk/efo/EFO_0008074 GCST90179278 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-X-C motif chemokine 1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 3 level of growth-regulated alpha protein in blood serum http://purl.obolibrary.org/obo/OBA_2044955 GCST90179279 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. C-X-C motif chemokine 16 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90179280 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Decorin levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 decorin measurement http://www.ebi.ac.uk/efo/EFO_0020315 GCST90179281 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. 2,4-dienoyl-CoA reductase,mitochondrial levels 2,850 Greek (founder/geneitc isolate) individuals NA Illumina [30468235] 0 level of 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041262 GCST90179282 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Dickkopf-related protein 1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90179283 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Protein delta homolog 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 level of protein delta homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041313 GCST90179284 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Dipeptidyl peptidase 2 levels 2,843 Greek (founder/geneitc isolate) individuals NA Illumina [30427946] 2 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90179285 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Epidermal growth factor receptor levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90179286 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Gamma-enolase levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 gamma-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021845 GCST90179287 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0020344 GCST90179288 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Ectonucleoside triphosphate diphosphohydrolase 5 levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30565780] 3 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90179289 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. epithelial cell adhesion molecule levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 epithelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010574 GCST90179290 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Osteoclast-associated immunoglobulin-like receptor levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 4 level of osteoclast-associated immunoglobulin-like receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042715 GCST90179316 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Heat shock 27 kDa protein levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 heat shock 27 kDa protein measurement http://www.ebi.ac.uk/efo/EFO_0010915 GCST90179317 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Intercellular adhesion molecule 2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90179318 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Alpha-L-iduronidase levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90179319 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Insulin-like growth factor-binding protein 1 levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30602880] 0 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90179320 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Insulin-like growth factor-binding protein 2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90179321 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Insulin-like growth factor-binding protein 7 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 5 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90179322 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Insulin-like growth factor-binding protein-like 1 levels 2,905 Greek (founder/geneitc isolate) individuals NA Illumina [30565519] 3 level of insulin-like growth factor-binding protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041991 GCST90179323 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Low affinity immunoglobulin gamma Fc region receptor II-b levels 2,850 Greek (founder/geneitc isolate) individuals NA Illumina [30476446] 3 low affinity immunoglobulin gamma Fc region receptor II-b measurement http://www.ebi.ac.uk/efo/EFO_0021970 GCST90179324 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-6 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90179337 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Pro-interleukin-16 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 pro‐interleukin‐16 measurement http://www.ebi.ac.uk/efo/EFO_0010629 GCST90179325 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-17D levels 2,856 Greek (founder/geneitc isolate) individuals NA Illumina [30480630] 2 interleukin-17D measurement http://www.ebi.ac.uk/efo/EFO_0021976 GCST90179326 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-17 receptor A levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 6 interleukin 17 receptor A measurement http://www.ebi.ac.uk/efo/EFO_0008175 GCST90179327 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-18 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 interleukin 18 measurement http://www.ebi.ac.uk/efo/EFO_0004581 GCST90179328 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-18-binding protein levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 interleukin-18-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020495 GCST90179329 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-1 receptor antagonist protein levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90179330 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-1 receptor-like 2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 5 interleukin 1 receptor-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0008169 GCST90179331 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-1 receptor type 1 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90179332 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-1 receptor type 2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90179333 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-27 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [29477231] 2 interleukin-27 measurement http://www.ebi.ac.uk/efo/EFO_0010916 GCST90179334 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-2 receptor subunit alpha levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 3 interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0010587 GCST90179335 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-4 receptor subunit alpha levels 2,849 Greek (founder/geneitc isolate) individuals NA Illumina [30467893] 1 interleukin-4 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020507 GCST90179336 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Interleukin-6 receptor subunit alpha levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90179338 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Integrin beta-2 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 level of integrin beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040372 GCST90179339 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Integrin beta-7 levels 2,416 Greek (founder/geneitc isolate) individuals NA Illumina [29716487] 1 level of integrin beta-7 in blood serum http://purl.obolibrary.org/obo/OBA_2042054 GCST90179340 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Ephrin type-B receptor 4 levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30603483] 1 ephrin type-b receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020354 GCST90179291 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Fatty acid-binding protein,intestinal levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 level of fatty acid-binding protein, intestinal in blood serum http://purl.obolibrary.org/obo/OBA_2041538 GCST90179292 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Fatty acid-binding protein, adipocyte levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 0 fatty acid-binding protein, adipocyte measurement http://www.ebi.ac.uk/efo/EFO_0010914 GCST90179293 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Protein FAM3C levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 0 level of protein FAM3C in blood serum http://purl.obolibrary.org/obo/OBA_2044299 GCST90179294 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Tumor necrosis factor receptor superfamily member 6 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90179295 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Fructose-1,6-bisphosphatase 1 levels 2,457 Greek (founder/geneitc isolate) individuals NA Illumina [29788509] 0 level of fructose-1,6-bisphosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041555 GCST90179296 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Fc receptor-like protein 1 levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 level of Fc receptor-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041563 GCST90179297 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Fibroblast growth factor 21 levels 2,855 Greek (founder/geneitc isolate) individuals NA Illumina [30472876] 2 fibroblast growth factor 21 measurement http://www.ebi.ac.uk/efo/EFO_0010783 GCST90179298 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Fibroblast growth factor 23 levels 2,843 Greek (founder/geneitc isolate) individuals NA Illumina [30459352] 0 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90179299 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Peptidyl-prolyl cis-trans isomerase FKBP4 levels 2,125 Greek (founder/geneitc isolate) individuals NA Illumina [29214892] 0 level of peptidyl-prolyl cis-trans isomerase FKBP4 in blood serum http://purl.obolibrary.org/obo/OBA_2044962 GCST90179300 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Follistatin levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 follistatin measurement http://www.ebi.ac.uk/efo/EFO_0010614 GCST90179301 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Galanin peptide levels 2,906 Greek (founder/geneitc isolate) individuals NA Illumina [30566327] 1 galanin peptides measurement http://www.ebi.ac.uk/efo/EFO_0010615 GCST90179302 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Galectin-3 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 2 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90179303 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Galectin-4 levels 2,923 Greek (founder/geneitc isolate) individuals NA Illumina [30603773] 1 galectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020398 GCST90179304 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Galectin-9 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 galectin-9 measurement http://www.ebi.ac.uk/efo/EFO_0021863 GCST90179305 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Growth/differentiation factor 15 levels 2,921 Greek (founder/geneitc isolate) individuals NA Illumina [30601020] 0 growth differentiation factor 15 measurement http://www.ebi.ac.uk/efo/EFO_0009181 GCST90179306 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Growth/differentiation factor 2 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 growth/differentiation factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020428 GCST90179307 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Growth hormone levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 growth hormone measurement http://www.ebi.ac.uk/efo/EFO_0008438 GCST90179308 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Gastric intrinsic factor levels 2,855 Greek (founder/geneitc isolate) individuals NA Illumina [30477624] 2 level of cobalamin binding intrinsic factor in blood serum http://purl.obolibrary.org/obo/OBA_2041717 GCST90179309 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Lactoylglutathione lyase levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 1 level of lactoylglutathione lyase in blood serum http://purl.obolibrary.org/obo/OBA_2041731 GCST90179310 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Granulins levels 2,922 Greek (founder/geneitc isolate) individuals NA Illumina [30603226] 3 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90179311 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Gastrotropin levels 2,602 Greek (founder/geneitc isolate) individuals NA Illumina [29590422] 0 level of gastrotropin in blood serum http://purl.obolibrary.org/obo/OBA_2041539 GCST90179312 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Hydroxyacid oxidase 1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 0 level of 2-hydroxyacid oxidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041836 GCST90179313 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Proheparin-binding EGF-like growth factor levels 2,857 Greek (founder/geneitc isolate) individuals NA Illumina [30481047] 1 proheparin-binding EGF-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010924 GCST90179314 Genome-wide sequencing [HiSeqX] 2023-06-19 36349687 Png G 2022-11-09 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/36349687 Identifying causal serum protein-cardiometabolic trait relationships using whole genome sequencing. Heme oxygenase 1 levels 2,858 Greek (founder/geneitc isolate) individuals NA Illumina [30481946] 2 level of heme oxygenase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041895 GCST90179315 Genome-wide sequencing [HiSeqX] 2022-11-29 36376295 Levin MG 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376295 Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure. Heart failure 5,791 African ancestry cases, 20,883 African ancestry controls, 1,170 admixed ancestry cases, 13,217 admixed ancestry controls, 12,665 East Asian ancestry cases, 245,263 East Asian ancestry controls, 95,524 European ancestry cases, 1,270,968 European ancestry controls 48,886 European ancestry cases, 279,185 European ancestry controls Affymetrix, Illumina [19309419] (imputed) 44 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90162626 Genome-wide genotyping array 2022-11-29 36376295 Levin MG 2022-11-14 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36376295 Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure. Heart failure (multivariate analysis) 17,917 African ancestry individuals, 4,293 admixed ancestry individuals, 47,934 East Asian ancestry individuals, 343,120 European ancestry individuals NA Affymetrix, Illumina [NR] 61 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90239776 Genome-wide genotyping array 2023-01-10 36192519 Praveen K 2022-10-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36192519 ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma. Intraocular pressure 129,207 European ancestry individuals NA Affymetrix, Illumina [NR] (imputed) 1 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90244183 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Body mass index (aged 40-50 years) 88,977 European ancestry individuals NA Affymetrix [5664578] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244560 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Body fat percentage (aged 40-50 years) 87,887 European ancestry individuals NA Affymetrix [5664578] (imputed) 1 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90244561 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Waist-hip ratio (aged 40-50 years) 89,060 European ancestry individuals NA Affymetrix [5664578] (imputed) 1 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90244562 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Waist circumference (aged 40-50 years) 89,076 European ancestry individuals NA Affymetrix [5664578] (imputed) 4 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90244563 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Hip circumference (aged 40-50 years) 89,062 European ancestry individuals NA Affymetrix [5664578] (imputed) 0 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90244564 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Body mass index (aged 64-69 years) 85,009 European ancestry individuals NA Affymetrix [5664578] (imputed) 4 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244565 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Body fat percentage (aged 64-69 years) 83,345 European ancestry individuals NA Affymetrix [5664578] (imputed) 1 body fat percentage http://www.ebi.ac.uk/efo/EFO_0007800 GCST90244566 Genome-wide genotyping array 2022-11-28 36271874 Hoffmann TJ 2022-10-22 Genetics www.ncbi.nlm.nih.gov/pubmed/36271874 A large genome-wide association study of QT interval length utilizing electronic health records. QT interval 62,976 European ancestry individuals, 6,238 Hispanic or Latin American individuals, 5,034 East Asian ancestry individuals, 2,437 African American individuals, 310 South Asian ancestry individuals NA NR [24475902] (imputed) 9 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90165290 Genome-wide genotyping array 2022-11-28 36271874 Hoffmann TJ 2022-10-22 Genetics www.ncbi.nlm.nih.gov/pubmed/36271874 A large genome-wide association study of QT interval length utilizing electronic health records. QT interval 86,165 European ancestry individuals, 13,975 Hispanic or Latin American individuals, 5,034 East Asian ancestry individuals, 8,457 African American individuals, 310 South Asian ancestry individuals, 1,631 Asian ancestry individuals, 1,370 Native Hawaiian ancestry individuals, 226 Native American ancestry individuals, 364 individuals NA NR [33042613] (imputed) 19 QT interval http://www.ebi.ac.uk/efo/EFO_0004682 GCST90165291 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Waist-hip ratio (aged 64-69 years) 85,152 European ancestry individuals NA Affymetrix [5664578] (imputed) 2 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90244567 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Waist circumference (aged 64-69 years) 85,157 European ancestry individuals NA Affymetrix [5664578] (imputed) 1 waist circumference http://www.ebi.ac.uk/efo/EFO_0004342 GCST90244568 Genome-wide genotyping array 2023-01-12 36276968 Chung JY 2022-10-07 Front Genet www.ncbi.nlm.nih.gov/pubmed/36276968 Identification of five genetic variants with differential effects on obesity-related traits based on age. Hip circumference (aged 64-69 years) 85,156 European ancestry individuals NA Affymetrix [5664578] (imputed) 2 hip circumference http://www.ebi.ac.uk/efo/EFO_0005093 GCST90244569 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Profile nasal area) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 113 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277944 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Nasal bridge angle) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277945 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Nasolabial angle) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 13 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277946 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Profile nasal angle) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 66 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277947 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right upper lip thickness) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277948 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left upper lip thickness) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277949 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid peak width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277950 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid peak width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 9 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277951 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid width) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277953 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of er1) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277954 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of er2) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277955 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of er3) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277956 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of er4) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277957 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of er5) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277958 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of er6) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277959 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of er7) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277960 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of el1) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277961 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of el2) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277962 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of el3) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277963 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of el4) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277964 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of el5) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277965 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of el6) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277966 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Tangent line angle of el7) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277967 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid peak position ratio) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277968 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid peak position ratio) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277969 Genome-wide genotyping array 2022-11-10 35320144 Klimentidis YC 2022-03-11 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/35320144 Genome-wide Association Study of Liking for Several Types of Physical Activity in the UK Biobank and Two Replication Cohorts. Liking for working up a sweat 158,189 European ancestry individuals 9,345 European ancestry individuals Affymetrix [11353280] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90204194 Genome-wide genotyping array 2022-11-10 35320144 Klimentidis YC 2022-03-11 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/35320144 Genome-wide Association Study of Liking for Several Types of Physical Activity in the UK Biobank and Two Replication Cohorts. Liking for going to the gym 140,015 European ancestry individuals 8,737 European ancestry individuals Affymetrix [11353280] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90204195 Genome-wide genotyping array 2022-11-10 35320144 Klimentidis YC 2022-03-11 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/35320144 Genome-wide Association Study of Liking for Several Types of Physical Activity in the UK Biobank and Two Replication Cohorts. Liking for bicycling 148,803 European ancestry individuals 9,360 European ancestry individuals Affymetrix [11353280] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90204196 Genome-wide genotyping array 2022-11-10 35320144 Klimentidis YC 2022-03-11 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/35320144 Genome-wide Association Study of Liking for Several Types of Physical Activity in the UK Biobank and Two Replication Cohorts. Liking for exercising with others 153,358 European ancestry individuals 9,194 European ancestry individuals Affymetrix [11353280] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90204197 Genome-wide genotyping array 2022-11-10 35320144 Klimentidis YC 2022-03-11 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/35320144 Genome-wide Association Study of Liking for Several Types of Physical Activity in the UK Biobank and Two Replication Cohorts. Liking for exercising alone 156,371 European ancestry individuals 9,157 European ancestry individuals Affymetrix [11353280] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90204198 Genome-wide genotyping array 2022-11-10 35320144 Klimentidis YC 2022-03-11 Med Sci Sports Exerc www.ncbi.nlm.nih.gov/pubmed/35320144 Genome-wide Association Study of Liking for Several Types of Physical Activity in the UK Biobank and Two Replication Cohorts. Overall physical activity liking 151,347 European ancestry individuals 9,158 European ancestry individuals Affymetrix [9780636] (imputed) 0 physical activity measurement http://www.ebi.ac.uk/efo/EFO_0008002 GCST90204199 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid slant) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277970 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid slant) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277971 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid medial slant) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277972 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid medial slant) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277973 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid lateral slant) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277974 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid lateral slant) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277975 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid average curvature) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277976 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Right eyelid maximal curvature) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277977 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid average curvature) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277978 Genome-wide genotyping array 2023-08-21 37415797 Cho HW 2023-04-25 Forensic Sci Res www.ncbi.nlm.nih.gov/pubmed/37415797 Effect of genetic variants in UBE2O and TPK1 on facial morphology of Koreans. Facial morphology (Left eyelid maximal curvature) 4,179 Korean ancestry individuals NA NR [8056211] (imputed) 0 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90277979 Genome-wide genotyping array 2022-11-21 36324662 Suppli NP 2021-11-09 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324662 Genome-wide by Environment Interaction Study of Stressful Life Events and Hospital-Treated Depression in the iPSYCH2012 Sample. Major depressive disorder 18,532 European ancestry cases, 20,184 European ancestry controls NA Illumina [496162] (imputed) 1 major depressive disorder http://purl.obolibrary.org/obo/MONDO_0002009 GCST90239707 Genome-wide genotyping array 2022-11-21 36324662 Suppli NP 2021-11-09 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324662 Genome-wide by Environment Interaction Study of Stressful Life Events and Hospital-Treated Depression in the iPSYCH2012 Sample. Stressful life events 38,716 European ancestry individuals NA Illumina [496162] (imputed) 0 stressful life event measurement http://www.ebi.ac.uk/efo/EFO_0007781 GCST90239708 Genome-wide genotyping array 2022-11-21 36324662 Suppli NP 2021-11-09 Biol Psychiatry Glob Open Sci www.ncbi.nlm.nih.gov/pubmed/36324662 Genome-wide by Environment Interaction Study of Stressful Life Events and Hospital-Treated Depression in the iPSYCH2012 Sample. Major depressive disorder (stressful life events interaction) 18,532 European ancestry depression cases, 20,184 European ancestry depression controls 22,880 European ancestry depression cases, 50,378 European ancestry depression controls Illumina [496162] (imputed) 0 stressful life event measurement, major depressive disorder http://www.ebi.ac.uk/efo/EFO_0007781, http://purl.obolibrary.org/obo/MONDO_0002009 GCST90239709 Genome-wide genotyping array 2023-01-13 36292730 Islam MR 2022-10-12 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36292730 Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes. Migraine or type 2 diabetes 74,124 European ancestry type 2 diabetes cases, 102,084 European ancestry migraine cases, 1,595,263 European ancestry controls NA NR [NR] 39 migraine disorder, type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005277, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90244660 Genome-wide genotyping array 2023-01-13 36292730 Islam MR 2022-10-12 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36292730 Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes. Headache or type 2 diabetes 74,124 European ancestry type 2 diabetes cases, 71,672 European ancestry headache cases, 1,112,725 European ancestry controls NA NR [NR] 18 Headache, type 2 diabetes mellitus http://purl.obolibrary.org/obo/HP_0002315, http://purl.obolibrary.org/obo/MONDO_0005148 GCST90244661 Genome-wide genotyping array 2022-11-25 35461751 Nakabuye M 2022-03-26 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35461751 Genetic loci implicated in meta-analysis of body shape in Africans. Body shape (principal component analysis) 8,769 African ancestry individuals NA Illumina [NR] (imputed) 1 body shape measurement http://www.ebi.ac.uk/efo/EFO_0801227 GCST90104902 Genome-wide genotyping array 2022-11-25 35461751 Nakabuye M 2022-03-26 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35461751 Genetic loci implicated in meta-analysis of body shape in Africans. Body shape (principal component analysis) 5,579 African ancestry women NA Illumina [NR] (imputed) 4 body shape measurement http://www.ebi.ac.uk/efo/EFO_0801227 GCST90104903 Genome-wide genotyping array 2022-11-25 35461751 Nakabuye M 2022-03-26 Nutr Metab Cardiovasc Dis www.ncbi.nlm.nih.gov/pubmed/35461751 Genetic loci implicated in meta-analysis of body shape in Africans. Body shape (principal component analysis) 3,423 African ancestry men NA Illumina [NR] (imputed) 1 body shape measurement http://www.ebi.ac.uk/efo/EFO_0801227 GCST90104904 Genome-wide genotyping array 2022-12-08 35386719 Baranova A 2022-03-21 Front Immunol www.ncbi.nlm.nih.gov/pubmed/35386719 Causal Association and Shared Genetics Between Asthma and COVID-19. Asthma or COVID-19 (pleiotropy) 6,406 European ancestry COVID-19 cases, 86,008 European ancestry asthma cases, 2,478 asthma cases, 1,337,407 European ancestry controls, 12,540 controls NA NR [NR] 2 asthma, COVID-19 http://purl.obolibrary.org/obo/MONDO_0004979, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104644 Genome-wide genotyping array 2023-04-14 36624241 Rajagopal VM 2023-01-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36624241 Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. School performance E-factor 1 (overall performance) 30,982 Danish ancestry individuals NA Illumina [6391200] (imputed) 4 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90267548 Genome-wide genotyping array 2023-04-14 36624241 Rajagopal VM 2023-01-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36624241 Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. School performance E-factor 2 (language performance relative to maths) 30,982 Danish ancestry individuals NA Illumina [6391200] (imputed) 2 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90267549 Genome-wide genotyping array 2023-04-14 36624241 Rajagopal VM 2023-01-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36624241 Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. School performance E-factor 3 (oral performance relative to written) 30,982 Danish ancestry individuals NA Illumina [6391200] (imputed) 1 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90267550 Genome-wide genotyping array 2023-04-14 36624241 Rajagopal VM 2023-01-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36624241 Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. School performance E-factor 4 (Danish performance relative to English) 30,982 Danish ancestry individuals NA Illumina [6391200] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90267551 Genome-wide genotyping array 2023-04-14 36624241 Rajagopal VM 2023-01-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36624241 Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. School performance E-factor 1 (overall performance) 4,547 European ancestry individuals NA Affymetrix, Illumina [5266884] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90267552 Genome-wide genotyping array 2023-04-14 36624241 Rajagopal VM 2023-01-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36624241 Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity. School performance E-factor 2 (language performance relative to maths) 4,547 European ancestry individuals NA Affymetrix, Illumina [5266884] (imputed) 0 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90267553 Genome-wide genotyping array 2023-02-13 36653477 Helkkula P 2023-01-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36653477 Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population. Varicose veins 13,045 Finnish ancestry female cases, 103,987 Finnish ancestry female controls NA Affymetrix, Illumina [16955345] (imputed) 1 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90225499 Genome-wide genotyping array 2023-02-13 36653477 Helkkula P 2023-01-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36653477 Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population. Varicose veins 3,982 Finnish ancestry male cases, 86,041 Finnish ancestry male controls NA Affymetrix, Illumina [16380437] (imputed) 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90225500 Genome-wide genotyping array 2023-02-13 36653477 Helkkula P 2023-01-18 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36653477 Genome-wide association study of varicose veins identifies a protective missense variant in GJD3 enriched in the Finnish population. Varicose veins 17,027 Finnish ancestry cases, 190,028 Finnish ancestry controls NA Affymetrix, Illumina [13541466] (imputed) 49 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90246234 Genome-wide genotyping array 2023-01-13 36222912 Badrinarayanan L 2022-10-12 Mol Genet Genomics www.ncbi.nlm.nih.gov/pubmed/36222912 Whole-genome sequencing unravels novel genetic determinants and regulatory pathways associated with triamcinolone acetonide-induced ocular hypertension. Triamcinolone acetonide-induced ocular hypertension 52 Indian ancestry individuals NA Illumina [7042908] 40 ocular hypertension, response to triamcinolone acetonide http://www.ebi.ac.uk/efo/EFO_1001069, http://www.ebi.ac.uk/efo/EFO_0006954 GCST90244659 Genome-wide sequencing 2023-01-13 36223920 Chen YC 2022-10-12 Clin J Am Soc Nephrol www.ncbi.nlm.nih.gov/pubmed/36223920 Genome-Wide Association Study for eGFR in a Taiwanese Population. Estimated glomerular filtration rate 10,008 Taiwanese ancestry individuals up to 110,517 European ancestry individuals, up to 16,840 African American individuals Affymetrix [6553511] (imputed) 6 glomerular filtration rate http://www.ebi.ac.uk/efo/EFO_0005208 GCST90244663 Genome-wide genotyping array 2023-02-08 36451823 Li P 2022-11-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36451823 Pilot genome-wide association study of antibody response to inactivated SARS-CoV-2 vaccines. IgG antibody levels in response to SARS-CoV-2 vaccination 168 East Asian ancestry individuals NA NR [5089908] (imputed) 8 anti-SARS-CoV-2 IgG measurement, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803358, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90244756 Genome-wide genotyping array 2023-02-08 36451823 Li P 2022-11-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36451823 Pilot genome-wide association study of antibody response to inactivated SARS-CoV-2 vaccines. Total antibody levels in response to SARS-CoV-2 vaccination 168 East Asian ancestry individuals NA NR [5089908] (imputed) 16 SARS-CoV-2 antibody measurement, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803360, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90244757 Genome-wide genotyping array 2023-02-08 36451823 Li P 2022-11-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36451823 Pilot genome-wide association study of antibody response to inactivated SARS-CoV-2 vaccines. Neutral antibody levels in response to SARS-CoV-2 vaccination 168 East Asian ancestry individuals NA NR [5089908] (imputed) 17 response to COVID-19 vaccine, SARS-CoV-2 neutralizing antibody measurement http://www.ebi.ac.uk/efo/EFO_0803362, http://www.ebi.ac.uk/efo/EFO_0803359 GCST90244758 Genome-wide genotyping array 2023-02-08 36451823 Li P 2022-11-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36451823 Pilot genome-wide association study of antibody response to inactivated SARS-CoV-2 vaccines. IgA antibody levels in response to SARS-CoV-2 vaccination 8 East Asian ancestry cases, 160 East Asian ancestry controls NA NR [5089908] (imputed) 0 SARS-CoV-2 antibody measurement, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803360, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90244759 Genome-wide genotyping array 2023-02-08 36451823 Li P 2022-11-14 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36451823 Pilot genome-wide association study of antibody response to inactivated SARS-CoV-2 vaccines. IgM antibody levels in response to SARS-CoV-2 vaccination 64 East Asian ancestry cases, 104 East Asian ancestry controls NA NR [5089908] (imputed) 0 SARS-CoV-2 antibody measurement, response to COVID-19 vaccine http://www.ebi.ac.uk/efo/EFO_0803360, http://www.ebi.ac.uk/efo/EFO_0803362 GCST90244760 Genome-wide genotyping array 2023-02-07 36508215 Feng X 2022-12-01 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/36508215 Association Between Genetic Risk, Adherence to Healthy Lifestyle Behavior, and Thyroid Cancer Risk. Thyroid cancer 986 European ancestry cases, 5,135 European ancestry controls NA Affymetrix [6562992] (imputed) 2 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90245887 Genome-wide genotyping array 2023-02-07 36508215 Feng X 2022-12-01 JAMA Netw Open www.ncbi.nlm.nih.gov/pubmed/36508215 Association Between Genetic Risk, Adherence to Healthy Lifestyle Behavior, and Thyroid Cancer Risk. Thyroid cancer 1,956 European ancestry cases, 101,924 European ancestry controls NA Affymetrix [NR] (imputed) 10 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90245888 Genome-wide genotyping array 2022-11-11 35069183 Trompet S 2022-01-05 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/35069183 The Pharmacogenetics of Statin Therapy on Clinical Events: No Evidence that Genetic Variation Affects Statin Response on Myocardial Infarction. Myocardial infraction risk reduction in statin users 4,212 European ancestry cases, 6,557 European ancestry controls 180 European ancestry cases, 1,345 European ancestry controls Affymetrix, Illumina [NR] (imputed) 3 response to statin, myocardial infarction http://purl.obolibrary.org/obo/GO_0036273, http://www.ebi.ac.uk/efo/EFO_0000612 GCST90102434 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Leucine levels 123,242 European ancestry individuals NA NR [8247959] 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90244690 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Isoleucine levels 123,242 European ancestry individuals NA NR [8247959] 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90244691 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Valine levels 123,242 European ancestry individuals NA NR [8247959] 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90244692 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Alanine levels 123,242 European ancestry individuals NA NR [8247959] 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90244693 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Phenylalanine levels 123,242 European ancestry individuals NA NR [8247959] 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90244694 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Tyrosine levels 123,242 European ancestry individuals NA NR [8247959] 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90244695 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Histidine levels 123,242 European ancestry individuals NA NR [8247959] 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90244696 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Glutamine levels 123,242 European ancestry individuals NA NR [8247959] 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90244697 Genome-wide genotyping array 2023-01-18 36307799 Lin C 2022-10-28 BMC Med www.ncbi.nlm.nih.gov/pubmed/36307799 The causal associations of circulating amino acids with blood pressure: a Mendelian randomization study. Glycine levels 123,242 European ancestry individuals NA NR [8247959] 0 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90244698 Genome-wide genotyping array 2023-02-14 36297114 Mompeo O 2022-10-21 Nutrients www.ncbi.nlm.nih.gov/pubmed/36297114 Genome-Wide Association Analysis of Over 170,000 Individuals from the UK Biobank Identifies Seven Loci Associated with Dietary Approaches to Stop Hypertension (DASH) Diet. Dietary Approaches to Stop Hypertension (DASH) diet 173,701 European ancestry individuals NA Affymetrix [12000000] (imputed) 7 dietary approaches to stop hypertension diet http://www.ebi.ac.uk/efo/EFO_0803365 GCST90244669 Genome-wide genotyping array 2023-01-17 36266505 Doust C 2022-10-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36266505 Discovery of 42 genome-wide significant loci associated with dyslexia. Dyslexia 51,800 European ancestry cases, 1,087,070 European ancestry controls NA Illumina [7995923] (imputed) 106 dyslexia http://www.ebi.ac.uk/efo/EFO_0005424 GCST90244674 Genome-wide genotyping array 2023-01-17 36266505 Doust C 2022-10-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36266505 Discovery of 42 genome-wide significant loci associated with dyslexia. Dyslexia 21,513 European ancestry male cases, 446,054 European ancestry male controls NA Illumina [7995923] (imputed) 0 dyslexia http://www.ebi.ac.uk/efo/EFO_0005424 GCST90244675 Genome-wide genotyping array 2023-01-17 36266505 Doust C 2022-10-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36266505 Discovery of 42 genome-wide significant loci associated with dyslexia. Dyslexia 30,287 European ancestry female cases, 641,016 European ancestry female controls NA Illumina [7995923] (imputed) 0 dyslexia http://www.ebi.ac.uk/efo/EFO_0005424 GCST90244676 Genome-wide genotyping array 2023-01-17 36266505 Doust C 2022-10-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36266505 Discovery of 42 genome-wide significant loci associated with dyslexia. Dyslexia 30,763 European ancestry cases aged <55 years, 582,276 European ancestry controls aged <55 years NA Illumina [7995923] (imputed) 0 dyslexia http://www.ebi.ac.uk/efo/EFO_0005424 GCST90244677 Genome-wide genotyping array 2023-01-17 36266505 Doust C 2022-10-20 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36266505 Discovery of 42 genome-wide significant loci associated with dyslexia. Dyslexia 21,037 European ancestry cases aged >=55 years, 504,794 European ancestry controls aged >=55 years NA Illumina [7995923] (imputed) 0 dyslexia http://www.ebi.ac.uk/efo/EFO_0005424 GCST90244678 Genome-wide genotyping array 2023-01-12 33951180 George DJ 2021-05-05 Cancer www.ncbi.nlm.nih.gov/pubmed/33951180 A prospective trial of abiraterone acetate plus prednisone in Black and White men with metastatic castrate-resistant prostate cancer. Time to prostate-specific antigen progression in metastatic castration-resistant prostate cancer 83 European or Black individuals NA Illumina [934674] 6 prostate-specific antigen measurement, disease progression measurement http://www.ebi.ac.uk/efo/EFO_0020660, http://www.ebi.ac.uk/efo/EFO_0008336 GCST90244572 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Fasting plasma glucose 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 56 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90244003 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Hemoglobin A1c levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 68 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90244004 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. HDL cholesterol levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 79 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90244005 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. LDL cholesterol levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 65 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90244006 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Triglyceride levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 65 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90244007 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Total cholesterol levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 91 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90244008 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Alanine aminotransferase levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 51 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90244009 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Aspartate aminotransferase levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 54 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90244010 Genome-wide genotyping array 2022-12-16 36333282 Kim YJ 2022-11-04 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36333282 The contribution of common and rare genetic variants to variation in metabolic traits in 288,137 East Asians. Gamma glutamyl transferase levels 288,127 East Asian ancestry individuals NA NR [6000000] (imputed) 82 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90244011 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Bedtime in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 0 sleep time http://www.ebi.ac.uk/efo/EFO_0005274 GCST90244771 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Waketime in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90244772 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Sleep duration in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90244773 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Wake after sleep onset in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 1 wake after sleep onset http://www.ebi.ac.uk/efo/EFO_0803363 GCST90244774 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Sleep efficiency in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 2 sleep efficiency http://www.ebi.ac.uk/efo/EFO_0803364 GCST90244775 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Number of awakenings in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 2 sleep quality http://www.ebi.ac.uk/efo/EFO_0005272 GCST90244776 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Longest sleep duration in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 1 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90244777 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Nap duration in severe depression 2,558 European ancestry individuals NA NR [7295914] (imputed) 4 short sleep http://www.ebi.ac.uk/efo/EFO_0004807 GCST90244778 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Bedtime in broad depression 13,657 European ancestry individuals NA NR [7304057] (imputed) 1 sleep time http://www.ebi.ac.uk/efo/EFO_0005274 GCST90244779 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Waketime in severe depression 13,657 European ancestry individuals NA NR [7295914] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90244780 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Sleep duration in broad depression 13,657 European ancestry individuals NA NR [7304057] (imputed) 1 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90244781 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Wake after sleep onset in broad depression 13,657 European ancestry individuals NA NR [7304057] (imputed) 0 wake after sleep onset http://www.ebi.ac.uk/efo/EFO_0803363 GCST90244782 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Sleep efficiency in broad depression 13,657 European ancestry individuals NA NR [7304057] (imputed) 2 sleep efficiency http://www.ebi.ac.uk/efo/EFO_0803364 GCST90244783 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Number of awakenings in broad depression 13,657 European ancestry individuals NA NR [7304057] (imputed) 3 sleep quality http://www.ebi.ac.uk/efo/EFO_0005272 GCST90244784 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Longest sleep duration in severe depression 13,657 European ancestry individuals NA NR [7295914] (imputed) 1 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90244785 Genome-wide genotyping array 2023-02-14 36463630 Melhuish Beaupre LM 2022-11-18 J Psychiatr Res www.ncbi.nlm.nih.gov/pubmed/36463630 Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects. Nap duration in broad depression 13,657 European ancestry individuals NA NR [7304057] (imputed) 2 short sleep http://www.ebi.ac.uk/efo/EFO_0004807 GCST90244786 Genome-wide genotyping array 2023-01-17 36209301 Baloni P 2022-10-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36209301 Multi-Omic analyses characterize the ceramide/sphingomyelin pathway as a therapeutic target in Alzheimer's disease. Sphingomyeline (d32:0) levels in Alzheimer disease 674 individuals NA Illumina [NR] 0 sphingomyelin 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0803336 GCST90244573 Genome-wide genotyping array 2023-01-17 36209301 Baloni P 2022-10-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36209301 Multi-Omic analyses characterize the ceramide/sphingomyelin pathway as a therapeutic target in Alzheimer's disease. Sphingomyeline (d34:1) levels in Alzheimer disease 674 individuals NA Illumina [NR] 0 sphingomyelin 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0803337 GCST90244574 Genome-wide genotyping array 2023-01-17 36209301 Baloni P 2022-10-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36209301 Multi-Omic analyses characterize the ceramide/sphingomyelin pathway as a therapeutic target in Alzheimer's disease. Sphingomyeline (d38:3) levels in Alzheimer disease 674 individuals NA Illumina [NR] 0 sphingomyelin 38:3 measurement http://www.ebi.ac.uk/efo/EFO_0803338 GCST90244575 Genome-wide genotyping array 2023-01-17 36209301 Baloni P 2022-10-08 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36209301 Multi-Omic analyses characterize the ceramide/sphingomyelin pathway as a therapeutic target in Alzheimer's disease. Sphingomyeline (d43:1/d34:1) ratio in Alzheimer disease 674 individuals NA Illumina [NR] 1 sphingomyelin 43:1/ 34:1 ratio measurement http://www.ebi.ac.uk/efo/EFO_0803339 GCST90244576 Genome-wide genotyping array 2023-01-10 34041566 Pungsrinont T 2021-05-26 Urolithiasis www.ncbi.nlm.nih.gov/pubmed/34041566 Association between intelectin-1 variation and human kidney stone disease in northeastern Thai population. Kidney stone disease 101 Thai ancestry cases, 105 Thai ancestry controls NA Affymetrix [652024] 0 nephrolithiasis http://www.ebi.ac.uk/efo/EFO_0004253 GCST90244570 Genome-wide genotyping array 2023-06-06 36348503 Real R 2022-11-09 Brain www.ncbi.nlm.nih.gov/pubmed/36348503 Association between the LRP1B and APOE loci in the development of Parkinson's disease dementia. Parkinson’s disease progression to dementia 3,923 European ancestry individuals NA Illumina [6107418] (imputed) 3 dementia, Parkinson disease, disease progression measurement http://purl.obolibrary.org/obo/MONDO_0001627, http://purl.obolibrary.org/obo/MONDO_0005180, http://www.ebi.ac.uk/efo/EFO_0008336 GCST90270129 Genome-wide genotyping array, Genome-wide sequencing 2023-05-16 37131961 Tomasoni M 2023-02-16 Ophthalmol Sci www.ncbi.nlm.nih.gov/pubmed/37131961 Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases. Retinal arterial distance factor tortuosity 62,751 European or unknown ancestry individuals 909 individuals NR [15600634] (imputed) 1 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90239688 Genome-wide genotyping array 2023-05-16 37131961 Tomasoni M 2023-02-16 Ophthalmol Sci www.ncbi.nlm.nih.gov/pubmed/37131961 Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases. Retinal venular distance factor tortuosity 62,751 European or unknown ancestry individuals 909 individuals NR [15600634] (imputed) 0 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90239689 Genome-wide genotyping array 2023-05-16 37131961 Tomasoni M 2023-02-16 Ophthalmol Sci www.ncbi.nlm.nih.gov/pubmed/37131961 Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases. Retinal distance factor tortuosity 62,751 European or unknown ancestry individuals 909 individuals NR [15600634] (imputed) 0 retinal vasculature measurement http://www.ebi.ac.uk/efo/EFO_0010554 GCST90239690 Genome-wide genotyping array 2023-06-02 36729213 Shiota M 2023-02-02 Cancer Immunol Immunother www.ncbi.nlm.nih.gov/pubmed/36729213 Effect of genetic polymorphisms on outcomes following nivolumab for advanced renal cell carcinoma in the SNiP-RCC trial. Objective response to nivolumab in renal cell carcinoma 112 Japanese ancestry individuals 110 Japanese ancestry individuals NR [659253] 0 response to nivolumab http://www.ebi.ac.uk/efo/EFO_0803366 GCST90270127 Genome-wide genotyping array 2022-12-06 34522458 Liu YS 2021-08-15 Am J Cancer Res www.ncbi.nlm.nih.gov/pubmed/34522458 Body mass index and type 2 diabetes and breast cancer survival: a Mendelian randomization study. Body mass index 24,000 individuals NA NR [NR] 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90053851 Genome-wide genotyping array 2022-12-06 34522458 Liu YS 2021-08-15 Am J Cancer Res www.ncbi.nlm.nih.gov/pubmed/34522458 Body mass index and type 2 diabetes and breast cancer survival: a Mendelian randomization study. Type 2 diabetes 24,000 individuals NA NR [NR] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90053852 Genome-wide genotyping array 2022-11-29 35347896 Li J 2022-03-29 Arthritis Rheumatol www.ncbi.nlm.nih.gov/pubmed/35347896 Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes through Integrative Genetic Analysis. Arthritis (juvenile idiopathic) 1,245 European ancestry cases, 9,250 European ancestry controls NA NR [NR] (imputed) 28 juvenile idiopathic arthritis http://www.ebi.ac.uk/efo/EFO_0002609 GCST90239777 Genome-wide genotyping array 2023-02-09 35902682 DiCorpo D 2022-07-28 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35902682 Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program. Fasting glucose 7,174 African American individuals, 2,217 East Asian ancestry individuals, 14,513 European ancestry individuals, 1,989 Hispanic or Latin American individuals, 914 Samoan ancestry individuals NA NR [64675008] 8 fasting blood glucose measurement http://www.ebi.ac.uk/efo/EFO_0004465 GCST90245986 Genome-wide sequencing 2023-02-09 35902682 DiCorpo D 2022-07-28 Commun Biol www.ncbi.nlm.nih.gov/pubmed/35902682 Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program. Fasting insulin 6,803 African American individuals, 572 East Asian ancestry individuals, 13,281 European ancestry individuals, 1,641 Hispanic or Latin American individuals, 914 Samoan ancestry individuals NA NR [58759883] 1 fasting blood insulin measurement http://www.ebi.ac.uk/efo/EFO_0004466 GCST90245987 Genome-wide sequencing 2023-01-16 36596879 Musolf AM 2023-01-03 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36596879 Rare variant analyses across multiethnic cohorts identify novel genes for refractive error. Mean spherical equivalent (Gene-based burden) 27,006 European, Asian unspecified ancestry individuals NA Affymetrix, Illumina [Illumina HumanExome-12 v 1.1|Affymetrix UK BioBank Axiom Array] 0 refractive error http://purl.obolibrary.org/obo/MONDO_0004892 GCST90244057 Exome genotyping array [Illumina HumanExome-12 v 1.1|Affymetrix UK BioBank Axiom Array] 2022-12-09 35096005 Westerman KE 2022-01-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/35096005 Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity. COVID-19 (severe vs population) x sex interaction (joint test) 2,402 European ancestry cases, 375,649 European ancestry controls NA NR [NR] 15 sex interaction measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0008343, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90102527 Genome-wide genotyping array 2022-12-09 35096005 Westerman KE 2022-01-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/35096005 Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity. COVID-19 (severe vs population) x sex interaction 2,402 European ancestry cases, 375,649 European ancestry controls NA NR [NR] 4 sex interaction measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0008343, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90102528 Genome-wide genotyping array 2022-12-09 35096005 Westerman KE 2022-01-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/35096005 Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity. COVID-19 (severe vs population) x multiple deprivation index interaction (joint test) 2,402 European ancestry cases, 375,649 European ancestry controls NA NR [NR] 15 social deprivation, COVID-19 http://www.ebi.ac.uk/efo/EFO_0009696, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90102529 Genome-wide genotyping array 2022-12-09 35096005 Westerman KE 2022-01-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/35096005 Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity. COVID-19 (severe vs population) x multiple deprivation index interaction 2,402 European ancestry cases, 375,649 European ancestry controls NA NR [NR] 8 social deprivation, COVID-19 http://www.ebi.ac.uk/efo/EFO_0009696, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90102530 Genome-wide genotyping array 2022-12-09 35096005 Westerman KE 2022-01-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/35096005 Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity. COVID-19 (severe vs population) x cardiometabolic health status interaction (joint test) 2,402 European ancestry cases, 375,649 European ancestry controls NA NR [NR] 15 metabolic disease, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000589, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90102531 Genome-wide genotyping array 2022-12-09 35096005 Westerman KE 2022-01-12 Front Genet www.ncbi.nlm.nih.gov/pubmed/35096005 Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity. COVID-19 (severe vs population) x cardiometabolic health status interaction 2,402 European ancestry cases, 375,649 European ancestry controls NA NR [NR] 10 metabolic disease, COVID-19 http://www.ebi.ac.uk/efo/EFO_0000589, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90102532 Genome-wide genotyping array 2023-01-05 36070248 Cavalli M 2022-09-07 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/36070248 Genome-wide association study of liver enzyme elevation in an extended cohort of rheumatoid arthritis patients starting low-dose methotrexate. Alanine aminotransferase level after methotrexate initiation in rheumatoid arthritis 346 Swedish ancestry individuals NA Illumina [6074601] (imputed) 19 response to methotrexate, serum alanine aminotransferase measurement http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004735 GCST90244104 Genome-wide genotyping array 2023-01-05 36070248 Cavalli M 2022-09-07 Pharmacogenomics www.ncbi.nlm.nih.gov/pubmed/36070248 Genome-wide association study of liver enzyme elevation in an extended cohort of rheumatoid arthritis patients starting low-dose methotrexate. Alanine aminotransferase elevation after methotrexate initiation in rheumatoid arthritis (>1.5 × ULN) 346 Swedish ancestry individuals NA Illumina [6074601] (imputed) 5 response to methotrexate, serum alanine aminotransferase measurement http://purl.obolibrary.org/obo/GO_0031427, http://www.ebi.ac.uk/efo/EFO_0004735 GCST90244105 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C60:12 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 60:12 measurement http://www.ebi.ac.uk/efo/EFO_0010444 GCST90257813 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Campesterol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90257814 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cholesterol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90257815 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Coenzyme Q9 levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90257816 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Palmitoylethanolamide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257817 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sphingosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90257818 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C14:0 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010340 GCST90257819 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90257820 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C16:1 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90257821 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C16:0 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90257822 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:2 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90257823 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:1 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90257824 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:0 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90257825 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C20:5 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90257826 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C20:4 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90257827 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C20:3 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90257828 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C22:6 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90257829 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:0 Monoacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257833 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C30:0 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 30:0 measurement http://www.ebi.ac.uk/efo/EFO_0020052 GCST90257834 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C32:2 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 32.2 measurement http://www.ebi.ac.uk/efo/EFO_0020055 GCST90257835 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90257788 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:8 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:8 measurement http://www.ebi.ac.uk/efo/EFO_0010426 GCST90257789 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:7 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:7 measurement http://www.ebi.ac.uk/efo/EFO_0010425 GCST90257790 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:6 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90257791 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90257792 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90257793 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90257794 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:2 measurement http://www.ebi.ac.uk/efo/EFO_0010420 GCST90257795 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:1 measurement http://www.ebi.ac.uk/efo/EFO_0010419 GCST90257796 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:10 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:10 measurement http://www.ebi.ac.uk/efo/EFO_0010428 GCST90257797 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C55:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257798 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C20:0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801125 GCST90257799 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:9 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:9 measurement http://www.ebi.ac.uk/efo/EFO_0010436 GCST90257800 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C55:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257801 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:8 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90257802 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:7 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:7 measurement http://www.ebi.ac.uk/efo/EFO_0010434 GCST90257803 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:6 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90257804 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:5 measurement http://www.ebi.ac.uk/efo/EFO_0010432 GCST90257805 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:4 measurement http://www.ebi.ac.uk/efo/EFO_0010431 GCST90257806 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:3 measurement http://www.ebi.ac.uk/efo/EFO_0010430 GCST90257807 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:2 measurement http://www.ebi.ac.uk/efo/EFO_0010429 GCST90257808 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C58:11 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:11 measurement http://www.ebi.ac.uk/efo/EFO_0010438 GCST90257809 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90257810 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C58:10 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:10 measurement http://www.ebi.ac.uk/efo/EFO_0010437 GCST90257811 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C58:9 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:9 measurement http://www.ebi.ac.uk/efo/EFO_0010443 GCST90257812 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 diacylglycerol 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0020067 GCST90257738 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 diacylglycerol 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0020066 GCST90257739 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C42:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257740 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C43:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257741 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C44:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257742 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C44:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 44:1 measurement http://www.ebi.ac.uk/efo/EFO_0010399 GCST90257743 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90257744 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C44:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257745 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C45:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257746 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C45:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257747 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C45:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257748 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257749 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257750 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 46:2 measurement http://www.ebi.ac.uk/efo/EFO_0010402 GCST90257751 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 46:1 measurement http://www.ebi.ac.uk/efo/EFO_0010401 GCST90257752 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 46:0 measurement http://www.ebi.ac.uk/efo/EFO_0010400 GCST90257753 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C47:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257754 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90257755 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C47:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257756 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257757 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:4 measurement http://www.ebi.ac.uk/efo/EFO_0010407 GCST90257758 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90257759 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90257760 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90257761 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90257762 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:3 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0020059 GCST90257838 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:2 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90257839 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:1 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90257840 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:0 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:0 measurement http://www.ebi.ac.uk/efo/EFO_0020058 GCST90257841 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C30:0 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C30:0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0801129 GCST90257842 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:4 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90257843 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:3 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90257844 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:2 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90257845 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:1 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010354 GCST90257846 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:0 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257847 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C38:5 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0020067 GCST90257848 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C38:4 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0020066 GCST90257849 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C38:4 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0020066 GCST90257850 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C41:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257851 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C42:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257852 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:2 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90257853 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C43:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257854 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C43:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257855 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C44:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 NH4_C44:2 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801203 GCST90257856 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C44:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 NH4_C44:1 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801202 GCST90257857 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C44:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257858 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257859 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257860 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257861 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257862 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C49:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257763 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C49:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257764 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:6 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257765 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90257766 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:5 measurement http://www.ebi.ac.uk/efo/EFO_0010412 GCST90257767 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90257768 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90257769 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90257770 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90257771 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:0 measurement http://www.ebi.ac.uk/efo/EFO_0021480 GCST90257772 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C51:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257773 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C51:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90257774 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:7 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257775 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C51:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 51:0 measurement http://www.ebi.ac.uk/efo/EFO_0021481 GCST90257776 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90257777 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:6 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:6 measurement http://www.ebi.ac.uk/efo/EFO_0010418 GCST90257778 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:5 measurement http://www.ebi.ac.uk/efo/EFO_0010417 GCST90257779 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90257780 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90257781 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90257782 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:1 measurement http://www.ebi.ac.uk/efo/EFO_0010413 GCST90257783 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257784 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C53:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257785 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:9 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:9 measurement http://www.ebi.ac.uk/efo/EFO_0010427 GCST90257786 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C53:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90257787 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C22:5 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90257830 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C30:1 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257831 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C22:4 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021443 GCST90257832 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C32:1 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257836 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C32:0 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0020054 GCST90257837 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Taurine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90258238 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-hydroxytryptophan levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90258239 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Serotonin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90258240 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Gamma-aminobutyric acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 GABA measurement http://www.ebi.ac.uk/efo/EFO_0801160 GCST90258241 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Dimethylglycine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90258242 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phenylalanine-d8 levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phenylalanine-d8 measurement http://www.ebi.ac.uk/efo/EFO_0801214 GCST90258243 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Asymmetric dimethylarginine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 asymmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006522 GCST90258244 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Symmetric dimethylarginine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 symmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006523 GCST90258245 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-methylarginine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90258246 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Allantoin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90258247 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methylguanidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylguanidine measurement http://www.ebi.ac.uk/efo/EFO_0800011 GCST90258248 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminoisobutyric acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 2-aminoisobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0801100 GCST90258249 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Kynurenic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 kynurenic acid measurement http://www.ebi.ac.uk/efo/EFO_0010506 GCST90258250 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Carnosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnosine measurement http://www.ebi.ac.uk/efo/EFO_0010470 GCST90258251 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-carbamoyl-beta-alanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-carbamoyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0801186 GCST90258252 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thiamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 thiamine measurement http://www.ebi.ac.uk/efo/EFO_0010540 GCST90258253 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90258254 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Niacinamide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 niacinamide measurement http://www.ebi.ac.uk/efo/EFO_0010511 GCST90258255 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Betaine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90258256 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Choline levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90258257 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phosphocholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90258258 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-glycerophosphocholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 alpha-glycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0801110 GCST90258259 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Creatine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90258260 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Creatinine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90258261 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thyroxine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90258262 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-guanidinobutanoic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90258313 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-pyridoxate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90258314 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glutamate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90258315 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Piperine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90257106 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90257107 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90257108 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90257109 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90257110 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90257111 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:5 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90257112 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90257113 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:3 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90257114 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90257115 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:5 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90257116 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90257117 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Monoacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257118 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Monoacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257119 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:2 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 32.2 measurement http://www.ebi.ac.uk/efo/EFO_0020055 GCST90257120 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:1 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257121 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:0 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0020054 GCST90257122 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0020059 GCST90257123 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90257124 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90257125 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:0 measurement http://www.ebi.ac.uk/efo/EFO_0020058 GCST90257126 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90257127 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C10 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258288 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C10:2 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C10:2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801119 GCST90258289 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C12 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258290 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C12:1 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258291 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258292 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:1 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258293 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:2 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C14:2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801121 GCST90258294 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258295 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C18 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801122 GCST90258296 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methionine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90258297 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C18:1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801123 GCST90258298 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C18 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801122 GCST90258299 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C26 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258300 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methyladenosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 adenosine measurement http://www.ebi.ac.uk/efo/EFO_0010453 GCST90258301 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylguanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0801093 GCST90258302 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylguanosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0801094 GCST90258303 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylhistamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0801095 GCST90258304 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminooctanoate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90258305 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-deoxyuridine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90258306 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Aspartate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90258307 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-methylguanosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N2-methylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0800634 GCST90258308 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-(N-acetyl-L-cystein-S-yl) acetaminophen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 3-cystein-S-ylacetaminophen measurement http://www.ebi.ac.uk/efo/EFO_0021155 GCST90258309 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methylhistamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0801095 GCST90258310 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methylhistidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90258311 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-acetamidobutanoate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90258312 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:1 measurement http://www.ebi.ac.uk/efo/EFO_0010413 GCST90257178 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257179 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C53:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257180 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:9 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 triacylglycerol 54:9 measurement http://www.ebi.ac.uk/efo/EFO_0010427 GCST90257181 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C53:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90257182 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90257183 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:8 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:8 measurement http://www.ebi.ac.uk/efo/EFO_0010426 GCST90257184 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:7 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:7 measurement http://www.ebi.ac.uk/efo/EFO_0010425 GCST90257185 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:6 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:6 measurement http://www.ebi.ac.uk/efo/EFO_0010424 GCST90257186 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90257187 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90257188 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90257189 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:2 measurement http://www.ebi.ac.uk/efo/EFO_0010420 GCST90257190 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C54:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:1 measurement http://www.ebi.ac.uk/efo/EFO_0010419 GCST90257191 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:10 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 triacylglycerol 56:10 measurement http://www.ebi.ac.uk/efo/EFO_0010428 GCST90257192 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C55:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257193 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C20:0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801125 GCST90257194 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:9 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 triacylglycerol 56:9 measurement http://www.ebi.ac.uk/efo/EFO_0010436 GCST90257195 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C55:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257196 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:8 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90257197 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:7 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:7 measurement http://www.ebi.ac.uk/efo/EFO_0010434 GCST90257198 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:6 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90257199 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:5 measurement http://www.ebi.ac.uk/efo/EFO_0010432 GCST90257200 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:4 measurement http://www.ebi.ac.uk/efo/EFO_0010431 GCST90257201 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:3 measurement http://www.ebi.ac.uk/efo/EFO_0010430 GCST90257202 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Trimethylamine-N-oxide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 plasma trimethylamine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0005691 GCST90258263 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cytosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258264 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90258265 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 xanthosine measurement http://www.ebi.ac.uk/efo/EFO_0010549 GCST90258266 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pipecolic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0010468 GCST90258267 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylnicotinamide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90258268 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Butyrobetaine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 butyrobetaine measurement http://www.ebi.ac.uk/efo/EFO_0801118 GCST90258269 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Putrescine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 putrescine measurement http://www.ebi.ac.uk/efo/EFO_0021810 GCST90258270 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methionine sulfoxide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90258271 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Anserine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90258272 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258273 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C2 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258274 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Serine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90258275 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C3 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258276 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C3-DC-CH3 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C3-DC-CH3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801128 GCST90258277 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C4 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258278 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C4-OH Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C4-OH carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801150 GCST90258279 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C5 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801153 GCST90258280 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C5:1 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801153 GCST90258281 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C5-DC Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801153 GCST90258282 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C6 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258283 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C7 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C7 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801154 GCST90258284 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C8 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90258285 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Threonine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90258286 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C9 Carnitine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 C9 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801155 GCST90258287 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90257128 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90257129 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010354 GCST90257130 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:0 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257131 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90257132 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 diacylglycerol 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0020067 GCST90257133 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 diacylglycerol 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0020066 GCST90257134 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C42:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257135 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C43:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257136 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C44:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257137 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C44:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 44:1 measurement http://www.ebi.ac.uk/efo/EFO_0010399 GCST90257138 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90257139 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C44:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257140 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C45:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257141 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C45:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257142 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C45:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257143 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257144 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257145 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 46:2 measurement http://www.ebi.ac.uk/efo/EFO_0010402 GCST90257146 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 46:1 measurement http://www.ebi.ac.uk/efo/EFO_0010401 GCST90257147 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C46:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 46:0 measurement http://www.ebi.ac.uk/efo/EFO_0010400 GCST90257148 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C47:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257149 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90257150 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C47:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257151 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257152 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:4 measurement http://www.ebi.ac.uk/efo/EFO_0010407 GCST90257153 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:3 measurement http://www.ebi.ac.uk/efo/EFO_0010406 GCST90257154 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90257155 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90257156 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C48:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90257157 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C49:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257158 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C49:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257159 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:6 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257160 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90257161 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:5 measurement http://www.ebi.ac.uk/efo/EFO_0010412 GCST90257162 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:4 measurement http://www.ebi.ac.uk/efo/EFO_0010411 GCST90257163 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90257164 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90257165 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90257166 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C50:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:0 measurement http://www.ebi.ac.uk/efo/EFO_0021480 GCST90257167 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C51:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257168 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C51:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90257169 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:7 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257170 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C51:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 51:0 measurement http://www.ebi.ac.uk/efo/EFO_0021481 GCST90257171 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90257172 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:6 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:6 measurement http://www.ebi.ac.uk/efo/EFO_0010418 GCST90257173 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:5 measurement http://www.ebi.ac.uk/efo/EFO_0010417 GCST90257174 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90257175 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90257176 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C52:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90257177 Genome-wide genotyping array 2022-12-23 36470867 Krohn L 2022-12-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36470867 Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. Isolated REM sleep behavior disorder 1,061 European ancestry cases, 8,386 European ancestry controls NA Illumina [12140795] (imputed) 0 REM sleep behavior disorder http://www.ebi.ac.uk/efo/EFO_0007462 GCST90204200 Genome-wide genotyping array 2022-12-23 36470867 Krohn L 2022-12-05 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36470867 Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects. REM sleep behavior disorder (probable or isolated) 2,843 European ancestry cases, 139,636 European ancestry controls NA Illumina [12140795] (imputed) 6 REM sleep behavior disorder http://www.ebi.ac.uk/efo/EFO_0007462 GCST90244078 Genome-wide genotyping array 2023-08-24 36930802 Gagnon MF 2023-03-17 Blood Adv www.ncbi.nlm.nih.gov/pubmed/36930802 Interplay Between Hereditary and Acquired Factors Determine Neutrophil Counts in Aging Individuals. White blood cell count 2,465 French ancestry older women NA Illumina [6103606] (imputed) 1 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90278195 Genome-wide genotyping array 2023-08-24 36930802 Gagnon MF 2023-03-17 Blood Adv www.ncbi.nlm.nih.gov/pubmed/36930802 Interplay Between Hereditary and Acquired Factors Determine Neutrophil Counts in Aging Individuals. Neutrophil count 2,465 French ancestry older women NA Illumina [6103606] (imputed) 1 neutrophil count http://www.ebi.ac.uk/efo/EFO_0004833 GCST90278196 Genome-wide genotyping array 2023-08-24 36930802 Gagnon MF 2023-03-17 Blood Adv www.ncbi.nlm.nih.gov/pubmed/36930802 Interplay Between Hereditary and Acquired Factors Determine Neutrophil Counts in Aging Individuals. Platelet count 2,465 French ancestry older women NA Illumina [6103606] (imputed) 1 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90278197 Genome-wide genotyping array 2023-01-11 36207451 Gaddis N 2022-10-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36207451 Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. Opioid addiction 7,281 European ancestry cases, 297,550 European ancestry controls, 3,856 African American cases, 12,203 African American controls NA Illumina [15510920] (imputed) 117 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST90244554 Genome-wide genotyping array 2023-01-11 36207451 Gaddis N 2022-10-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36207451 Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. Opioid addiction (multi-trait analysis) 88,114 European ancestry individuals NA Illumina [2434903] (imputed) 3 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST90244555 Genome-wide genotyping array 2023-01-11 36207451 Gaddis N 2022-10-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36207451 Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. Opioid addiction 7,281 European ancestry cases, 297,550 European ancestry controls NA Illumina [NR] (imputed) 63 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST90244556 Genome-wide genotyping array 2023-01-11 36207451 Gaddis N 2022-10-07 Sci Rep www.ncbi.nlm.nih.gov/pubmed/36207451 Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. Opioid addiction 3,856 African American cases, 12,203 African American controls NA Illumina [NR] (imputed) 66 opioid dependence http://www.ebi.ac.uk/efo/EFO_0005611 GCST90244557 Genome-wide genotyping array 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (TET2 mutation) 3,918 European ancestry cases, 342,869 European ancestry controls 1,888 European ancestry cases, 135,106 European ancestry controls Affymetrix, Illumina [43187107] (imputed) 3 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165281 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (TP53 mutation) (gene burden) 393 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165282 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (TP53 mutation) 393 European ancestry cases, 342,869 European ancestry controls 301 European ancestry cases, 135,106 European ancestry controls Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165283 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Mosaic chromosomal alteration of the autosomes (gene burden) 10,752 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 chromosomal aberration http://www.ebi.ac.uk/efo/EFO_0000336 GCST90165284 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Mosaic chromosomal alteration of the autosomes 10,752 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 3 chromosomal aberration http://www.ebi.ac.uk/efo/EFO_0000336 GCST90165285 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Mosaic chromosomal alteration of the X chromosome (gene burden) 10,536 European ancestry cases, 201,132 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 chromosomal aberration http://www.ebi.ac.uk/efo/EFO_0000336 GCST90165286 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Mosaic chromosomal alteration of the X chromosome 10,536 European ancestry cases, 201,132 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 13 chromosomal aberration http://www.ebi.ac.uk/efo/EFO_0000336 GCST90165287 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Mosaic chromosomal alteration of the Y chromosome (gene burden) 35,406 European ancestry cases, 141,737 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 chromosomal aberration http://www.ebi.ac.uk/efo/EFO_0000336 GCST90165288 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Mosaic chromosomal alteration of the Y chromosome 35,406 European ancestry cases, 141,737 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 171 chromosomal aberration http://www.ebi.ac.uk/efo/EFO_0000336 GCST90165289 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-06 36171425 Kember RL 2022-09-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/36171425 Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. Opioid use disorder 8,968 African American cases, 79,530 African American controls, 24,867 European ancestry cases, 296,446 European ancestry controls, 2,527 Hispanic American cases, 32,334 Hispanic American controls, 1,399 African ancestry cases, 1,450 African ancestry controls NA Affymetrix [NR] (imputed) 8 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90244132 Genome-wide genotyping array 2023-01-06 36171425 Kember RL 2022-09-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/36171425 Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. Opioid use disorder 8,968 African American cases, 79,530 African American controls, 1,399 African ancestry cases, 1,450 African ancestry controls NA Affymetrix [NR] (imputed) 1 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90244133 Genome-wide genotyping array 2023-01-06 36171425 Kember RL 2022-09-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/36171425 Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. Opioid use disorder 24,867 European ancestry cases, 296,446 European ancestry controls NA Affymetrix [NR] (imputed) 5 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90244134 Genome-wide genotyping array 2023-01-06 36171425 Kember RL 2022-09-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/36171425 Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. Opioid use disorder (broad) 8,968 African American cases, 79,530 African American controls, 19,978 European ancestry cases, 282,607 European ancestry controls, 2,527 Hispanic American cases, 32,334 Hispanic American controls NA Affymetrix [NR] (imputed) 10 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90244135 Genome-wide genotyping array 2023-01-06 36171425 Kember RL 2022-09-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/36171425 Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. Opioid use disorder (broad) 8,968 African American cases, 79,530 African American controls NA Affymetrix [NR] (imputed) 2 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90244136 Genome-wide genotyping array 2023-01-06 36171425 Kember RL 2022-09-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/36171425 Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. Opioid use disorder (broad) 19,978 European ancestry cases, 282,607 European ancestry controls NA Affymetrix [NR] (imputed) 4 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90244137 Genome-wide genotyping array 2023-01-06 36171425 Kember RL 2022-09-28 Nat Neurosci www.ncbi.nlm.nih.gov/pubmed/36171425 Cross-ancestry meta-analysis of opioid use disorder uncovers novel loci with predominant effects in brain regions associated with addiction. Opioid use disorder (broad) 2,527 Hispanic American cases, 32,334 Hispanic American controls NA Affymetrix [NR] (imputed) 2 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90244138 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Alzheimer's disease 386 European ancestry cases, 2,206 European ancestry controls NA Illumina [14072053] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90244026 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Alzheimer's disease 182 European ancestry female cases, 978 European ancestry female controls NA Illumina [14072053] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90244027 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Alzheimer's disease 204 European ancestry male cases, 1,228 European ancestry male controls NA Illumina [14072053] (imputed) 2 Alzheimer disease http://purl.obolibrary.org/obo/MONDO_0004975 GCST90244028 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Dementia 424 European ancestry cases, 2,206 European ancestry controls NA Illumina [14072053] (imputed) 2 dementia http://purl.obolibrary.org/obo/MONDO_0001627 GCST90244029 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Dementia 203 European ancestry female cases, 978 European ancestry female controls NA Illumina [14072053] (imputed) 2 dementia http://purl.obolibrary.org/obo/MONDO_0001627 GCST90244030 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Dementia 221 European ancestry male cases, 1,228 European ancestry male controls NA Illumina [14072053] (imputed) 2 dementia http://purl.obolibrary.org/obo/MONDO_0001627 GCST90244031 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Alzheimer's disease in APOE e4+ carriers 150 European ancestry cases, 458 European ancestry controls NA Illumina [14072053] (imputed) 12 Alzheimer disease, APOE carrier status http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0007659 GCST90244032 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Alzheimer's disease in non-APOE e4 carriers 232 European ancestry cases, 1,739 European ancestry controls NA Illumina [14072053] (imputed) 47 Alzheimer disease, APOE carrier status http://purl.obolibrary.org/obo/MONDO_0004975, http://www.ebi.ac.uk/efo/EFO_0007659 GCST90244033 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Dementia in APOE e4+ carriers 159 European ancestry cases, 458 European ancestry controls NA Illumina [14072053] (imputed) 11 APOE carrier status, dementia http://www.ebi.ac.uk/efo/EFO_0007659, http://purl.obolibrary.org/obo/MONDO_0001627 GCST90244034 Genome-wide genotyping array 2022-12-21 35694926 Harper JD 2022-06-09 J Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/35694926 Genome-Wide Association Study of Incident Dementia in a Community-Based Sample of Older Subjects. Dementia in non-APOE e4 carriers 261 European ancestry cases, 1,739 European ancestry controls NA Illumina [14072053] (imputed) 32 APOE carrier status, dementia http://www.ebi.ac.uk/efo/EFO_0007659, http://purl.obolibrary.org/obo/MONDO_0001627 GCST90244035 Genome-wide genotyping array 2022-12-15 35512135 Cindi Z 2022-05-04 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/35512135 Pharmacogenetics of dolutegravir plasma exposure among Southern Africans living with HIV. Response to dolutegravir in HIV infection (area under the concentration-time curve) 284 Black individuals NA Illumina [NR] (imputed) 11 response to dolutegravir http://www.ebi.ac.uk/efo/EFO_0600017 GCST90243990 Genome-wide genotyping array 2022-12-15 35512135 Cindi Z 2022-05-04 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/35512135 Pharmacogenetics of dolutegravir plasma exposure among Southern Africans living with HIV. Bilirubin concentration in dolutegravir-treated HIV infection 284 Black individuals NA Illumina [NR] (imputed) 6 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90243991 Genome-wide genotyping array 2022-12-15 35512135 Cindi Z 2022-05-04 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/35512135 Pharmacogenetics of dolutegravir plasma exposure among Southern Africans living with HIV. Response to dolutegravir in HIV infection (clearance) 284 Black individuals NA Illumina [NR] (imputed) 8 response to dolutegravir http://www.ebi.ac.uk/efo/EFO_0600017 GCST90243992 Genome-wide genotyping array 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Telomere length (gene burden) 418,401 European ancestry individuals NA Affymetrix, Illumina [449587] (imputed) 0 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90165256 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Telomere length 418,401 European ancestry individuals NA Affymetrix, Illumina [63064759] (imputed) 482 telomere length http://www.ebi.ac.uk/efo/EFO_0004505 GCST90165257 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (ASXL1 mutation) (gene burden) 2,007 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [448200] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165258 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (ASXL1 mutation) 2,007 European ancestry cases, 342,869 European ancestry controls 1,007 European ancestry cases, 135,106 European ancestry controls Affymetrix, Illumina [61312138] (imputed) 1 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165259 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (without mosaic chromosomal alteration) (gene burden) 20,606 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [448606] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165260 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (without mosaic chromosomal alteration) 20,606 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [61816446] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165261 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) (gene burden) 375 African ancestry cases, 8,177 African ancestry controls NA Affymetrix, Illumina [341709] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165262 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) 375 African ancestry cases, 8,177 African ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165263 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) (gene burden) 101 East Asian ancestry cases, 2,044 East Asian ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165264 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) 101 East Asian ancestry cases, 2,044 East Asian ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165265 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) (gene burden) 25,657 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165266 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) 25,657 European ancestry cases, 342,869 European ancestry controls 9,523 European ancestry cases, 105,502 European ancestry controls Affymetrix, Illumina [43187107] (imputed) 4 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165267 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) (gene burden) 494 South Asian ancestry cases, 9,054 South Asian ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165268 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (with or without mosaic chromosomal alteration) 494 South Asian ancestry cases, 9,054 South Asian ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165269 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (DNMT3A mutation) (gene burden) 16,219 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165270 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (DNMT3A mutation) 16,219 European ancestry cases, 342,869 European ancestry controls 5,991 European ancestry cases, 135,106 European ancestry controls Affymetrix, Illumina [43187107] (imputed) 9 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165271 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (JAK2 mutation) (gene burden) 186 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165272 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (JAK2 mutation) 186 European ancestry cases, 342,869 European ancestry controls 95 European ancestry cases, 135,106 European ancestry controls Affymetrix, Illumina [43187107] (imputed) 1 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165273 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (PPM1D mutation) (gene burden) 652 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165274 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (PPM1D mutation) 652 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165275 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (SF3B1 mutation) (gene burden) 170 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165276 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (SF3B1 mutation) 170 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165277 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (SRSF2 mutation) (gene burden) 162 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165278 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (SRSF2 mutation) 162 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165279 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-11 36450978 Kessler MD 2022-11-30 Nature www.ncbi.nlm.nih.gov/pubmed/36450978 Common and rare variant associations with clonal haematopoiesis phenotypes. Clonal haematopoiesis of indeterminate potential (TET2 mutation) (gene burden) 3,918 European ancestry cases, 342,869 European ancestry controls NA Affymetrix, Illumina [43187107] (imputed) 0 clonal hematopoiesis http://www.ebi.ac.uk/efo/EFO_0010819 GCST90165280 Genome-wide genotyping array, Exome-wide sequencing [UK Biobank/UK BiLEVE Axiom Array] 2023-01-26 36551779 Groen In 't Woud S 2022-11-23 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551779 A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney. Congenital solitary functioning kidney 403 Dutch ancestry cases, 622 Dutch ancestry controls NA Illumina [9956431] (imputed) 6 renal agenesis, unilateral http://purl.obolibrary.org/obo/MONDO_0019636 GCST90244791 Genome-wide genotyping array 2023-01-26 36551779 Groen In 't Woud S 2022-11-23 Biomedicines www.ncbi.nlm.nih.gov/pubmed/36551779 A Genome-Wide Association Study into the Aetiology of Congenital Solitary Functioning Kidney. Congenital solitary functioning kidney 403 Dutch ancestry cases, 4,366 Dutch ancestry controls NA Illumina [9313318] (imputed) 26 renal agenesis, unilateral http://purl.obolibrary.org/obo/MONDO_0019636 GCST90244792 Genome-wide genotyping array 2023-01-20 34275906 Heilbron K 2021-07-15 J Parkinsons Dis www.ncbi.nlm.nih.gov/pubmed/34275906 Unhealthy Behaviours and Risk of Parkinson's Disease: A Mendelian Randomisation Study. Smoking status (ever vs never smokers) 863,802 European ancestry cases, 1,569,209 European ancestry controls NA Illumina [25208208] (imputed) 0 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90026534 Genome-wide genotyping array 2023-01-20 34275906 Heilbron K 2021-07-15 J Parkinsons Dis www.ncbi.nlm.nih.gov/pubmed/34275906 Unhealthy Behaviours and Risk of Parkinson's Disease: A Mendelian Randomisation Study. Body mass index 2,433,011 European ancestry individuals NA Illumina [25208208] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90026536 Genome-wide genotyping array 2023-01-04 35264675 Nishida N 2022-03-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35264675 Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19. COVID-19 462 Japanese ancestry cases, 1,193 Japanese ancestry controls NA Illumina [15167811] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104445 Genome-wide genotyping array 2023-01-04 35264675 Nishida N 2022-03-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35264675 Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19. COVID-19 (severe vs population) 99 Japanese ancestry cases, 1,193 Japanese ancestry controls NA Illumina [15167811] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104448 Genome-wide genotyping array 2023-01-04 35264675 Nishida N 2022-03-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35264675 Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19. COVID-19 (severe vs mild) 99 Japanese ancestry severe cases, 347 Japanese ancestry mild cases NA Illumina [15167811] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104451 Genome-wide genotyping array 2023-01-04 35264675 Nishida N 2022-03-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35264675 Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19. COVID-19 462 Japanese ancestry cases, 1,193 Japanese ancestry controls, 7,885 cases, 961,804 controls NA Illumina [15167811] (imputed) 3 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104447 Genome-wide genotyping array 2023-01-04 35264675 Nishida N 2022-03-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35264675 Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19. COVID-19 (severe vs population) 99 Japanese ancestry cases, 1,193 Japanese ancestry controls, 4,336 cases, 623,902 controls NA Illumina [15167811] (imputed) 2 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104450 Genome-wide genotyping array 2023-01-04 35264675 Nishida N 2022-03-09 Sci Rep www.ncbi.nlm.nih.gov/pubmed/35264675 Genetic association of IL17 and the importance of ABO blood group antigens in saliva to COVID-19. COVID-19 (severe vs mild) 99 Japanese ancestry severe cases, 347 Japanese ancestry mild cases, 269 severe cases, 688 mild cases NA Illumina [15167811] (imputed) 1 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90104453 Genome-wide genotyping array 2023-01-31 36379924 Strom NI 2022-11-15 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/36379924 Meta-analysis of genome-wide association studies of hoarding symptoms in 27,537 individuals. Hoarding symptoms 27,537 European ancestry individuals NA NR [6541342] (imputed) 23 hoarding disorder http://www.ebi.ac.uk/efo/EFO_0803361 GCST90244767 Genome-wide genotyping array 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Neuroticism (UKB data field 20127) 138,580 European ancestry individuals NA NR [299582] 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90103370 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Reported occurrences of cancer (UKB data field 40009) 170,769 European ancestry individuals NA NR [299582] 0 cancer http://purl.obolibrary.org/obo/MONDO_0004992 GCST90103371 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Pulse rate (UKB data field 4194) 84,171 European ancestry individuals NA NR [299582] 0 heart rate http://www.ebi.ac.uk/efo/EFO_0004326 GCST90103372 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Mean time to correctly identify matches (UKB data field 20023) 169,753 European ancestry individuals NA NR [299582] 0 cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0008354 GCST90103373 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of N39 (other disorders of urinary system) (UKB data field 132071) 17,451 European ancestry cases, 153,306 European ancestry controls NA NR [299582] 0 urinary system disease http://www.ebi.ac.uk/efo/EFO_0009690 GCST90103424 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of N92 (excessive, frequent and irregular menstruation) (UKB data field 132147) 10,711 European ancestry cases, 160,046 European ancestry controls NA NR [299582] 0 Menorrhagia http://purl.obolibrary.org/obo/HP_0000132 GCST90103425 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of O36 (maternal care for other known or suspected foetal problems) (UKB data field 132225) 898 European ancestry cases, 169,859 European ancestry controls NA NR [299582] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90103426 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I21 (acute myocardial infarction) (UKB data field 131299) 5,541 European ancestry cases, 165,216 European ancestry controls NA NR [299582] 0 acute myocardial infarction http://www.ebi.ac.uk/efo/EFO_0008583 GCST90103349 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Alcohol intake frequency (UKB data field 1558) 170,572 European ancestry individuals NA NR [299582] 0 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90103350 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of asthma report (UKB data field 42015) 22,473 European ancestry cases, 148,296 European ancestry controls NA NR [299582] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90103351 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Red blood cell erythrocyte count (UKB data field 30010) 166,352 European ancestry individuals NA NR [299582] 0 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90103376 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of chronic obstructive pulmonary disease report (UKB data field 42017) 5,757 European ancestry cases, 165,012 European ancestry controls NA NR [299582] 0 chronic obstructive pulmonary disease http://www.ebi.ac.uk/efo/EFO_0000341 GCST90103354 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of B07 (viral warts) (UKB data field 130189) 6,519 European ancestry cases, 164,238 European ancestry controls NA NR [299582] 0 common wart http://www.ebi.ac.uk/efo/EFO_0009662 GCST90103384 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Corneal hysteresis right (UKB data field 5256) 57,066 European ancestry individuals NA NR [299582] 0 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST90103356 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Corneal resistance factor left (UKB data field 5265) 56,937 European ancestry individuals NA NR [299582] 0 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST90103357 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of D64 (other anaemias) (UKB data field 130649) 9,443 European ancestry cases, 161,314 European ancestry controls NA NR [299582] 0 anemia (phenotype) http://www.ebi.ac.uk/efo/EFO_0004272 GCST90103386 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Age diabetes diagnosed (UKB data field 2976) 8,126 European ancestry cases, 162,643 European ancestry controls NA NR [299582] 0 age of onset of type 1 diabetes mellitus, age of onset of type 2 diabetes mellitus http://purl.obolibrary.org/obo/OBA_2001012, http://purl.obolibrary.org/obo/OBA_2001013 GCST90103359 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Date E11 first reported (non-insulin-dependent diabetes mellitus) (UKB data field 130708) 12,037 European ancestry cases, 158,732 European ancestry controls NA NR [299582] 0 age of onset of type 2 diabetes mellitus http://purl.obolibrary.org/obo/OBA_2001013 GCST90103360 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E05 (thyrotoxicosis [hyperthyroidism]) (UKB data field 130701) 2,581 European ancestry cases, 168,176 European ancestry controls NA NR [299582] 0 hyperthyroidism http://www.ebi.ac.uk/efo/EFO_0009189 GCST90103389 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Fluid intelligence score (UKB data field 20016) 84,429 European ancestry individuals NA NR [299582] 0 intelligence http://www.ebi.ac.uk/efo/EFO_0004337 GCST90103362 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Haematocrit percentage (UKB data field 30030) 166,352 European ancestry individuals NA NR [299582] 0 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90103363 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E11 (non-insulin-dependent diabetes mellitus) (UKB data field 130709) 12,037 European ancestry cases, 158,720 European ancestry controls NA NR [299582] 0 type 2 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005148 GCST90103391 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E14 (unspecified diabetes mellitus) (UKB data field 130715) 7,526 European ancestry cases, 163,231 European ancestry controls NA NR [299582] 0 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90103392 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E78 (disorders of lipoprotein metabolism and other lipidaemias) (UKB data field 130815) 38,221 European ancestry cases, 132,536 European ancestry controls NA NR [299582] 0 metabolic disease http://www.ebi.ac.uk/efo/EFO_0000589 GCST90103393 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E80 (disorders of porphyrin and bilirubin metabolism) (UKB data field 130819) 631 European ancestry cases, 170,126 European ancestry controls NA NR [299582] 0 porphyrin metabolism disease http://purl.obolibrary.org/obo/MONDO_0037821 GCST90103394 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of M45 (ankylosing spondylitis) (UKB data field 131913) 655 European ancestry cases, 170,102 European ancestry controls NA NR [299582] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90103423 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Probable recurrent major depression (moderate) (UKB data field 20124) 6,562 European ancestry cases, 164,207 European ancestry controls NA NR [299582] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90103374 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Probable recurrent major depression (moderate and severe) 10,397 European ancestry cases, 160,372 European ancestry controls NA NR [299582] 0 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90103375 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Morning/evening person (chronotype) (UKB data field 1180) 151,298 European ancestry individuals NA NR [299582] 0 chronotype measurement http://www.ebi.ac.uk/efo/EFO_0008328 GCST90103352 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Coffee intake (UKB data field 1498) 156,616 European ancestry individuals NA NR [299582] 0 coffee consumption measurement http://www.ebi.ac.uk/efo/EFO_0006781 GCST90103353 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Reticulocyte count (UKB data field 30250) 163,075 European ancestry individuals NA NR [299582] 0 reticulocyte count http://www.ebi.ac.uk/efo/EFO_0007986 GCST90103377 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Risk taking (UKB data field 2040) 39,937 European ancestry cases, 123,902 European ancestry controls NA NR [299582] 0 behavioural disinhibition measurement http://www.ebi.ac.uk/efo/EFO_0006946 GCST90103378 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Current tobacco smoking on most or all days (UKB data field 1239) 170,593 European ancestry individuals NA NR [299582] 0 smoking behaviour measurement http://www.ebi.ac.uk/efo/EFO_0005671 GCST90103379 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Standing height (UKB data field 50) 170,757 European ancestry individuals NA NR [299582] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90103380 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Volume of ventricular cerebrospinal fluid (normalised for head size) (UKB data field 25003) 19,266 European ancestry individuals NA NR [299582] 0 cerebrospinal fluid volume measurement http://www.ebi.ac.uk/efo/EFO_0008080 GCST90103381 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Volume of white matter (normalised for head size) (UKB data field 25007) 19,266 European ancestry individuals NA NR [299582] 0 white matter volume measurement http://www.ebi.ac.uk/efo/EFO_0008320 GCST90103382 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of B02 (zoster [herpes zoster]) (UKB data field 130179) 5,741 European ancestry cases, 165,016 European ancestry controls NA NR [299582] 0 Herpes Zoster http://www.ebi.ac.uk/efo/EFO_0006510 GCST90103383 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Corneal hysteresis left (UKB data field 5264) 56,937 European ancestry individuals NA NR [299582] 0 corneal hysteresis http://www.ebi.ac.uk/efo/EFO_0010066 GCST90103355 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of D50 (iron deficiency anaemia) (UKB data field 130623) 8,915 European ancestry cases, 161,842 European ancestry controls NA NR [299582] 0 Iron deficiency anemia http://purl.obolibrary.org/obo/HP_0001891 GCST90103385 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Corneal resistance factor right (UKB data field 5257) 57,066 European ancestry individuals NA NR [299582] 0 corneal resistance factor http://www.ebi.ac.uk/efo/EFO_0010067 GCST90103358 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of D86 (sarcoidosis) (UKB data field 130687) 637 European ancestry cases, 170,120 European ancestry controls NA NR [299582] 0 sarcoidosis http://purl.obolibrary.org/obo/MONDO_0019338 GCST90103387 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E03 (other hypothyroidism) (UKB data field 130697) 12,684 European ancestry cases, 158,073 European ancestry controls NA NR [299582] 0 hypothyroidism http://www.ebi.ac.uk/efo/EFO_0004705 GCST90103388 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. FEV1 FVC ratio Z score (UKB data field 20258) 134,872 European ancestry individuals NA NR [299582] 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90103361 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E10 (insulin-dependent diabetes mellitus) (UKB data field 130707) 1,467 European ancestry cases, 169,290 European ancestry controls NA NR [299582] 0 type 1 diabetes mellitus http://purl.obolibrary.org/obo/MONDO_0005147 GCST90103390 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Hair colour (natural, before greying) (UKB data field 1747) 162,633 European ancestry individuals NA NR [299582] 0 hair colour measurement http://www.ebi.ac.uk/efo/EFO_0007822 GCST90103364 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Heel bone mineral density (UKB data field 3148) 86,762 European ancestry individuals NA NR [299582] 0 heel bone mineral density http://www.ebi.ac.uk/efo/EFO_0009270 GCST90103365 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Age high blood pressure diagnosed (UKB data field 2966) 47,079 European ancestry cases, 123,690 European ancestry controls NA NR [299582] 0 hypertension, age at onset http://www.ebi.ac.uk/efo/EFO_0000537, http://www.ebi.ac.uk/efo/EFO_0004847 GCST90103366 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Intra-ocular pressure, Goldmann-correlated left (UKB data field 5263) 56,937 European ancestry individuals NA NR [299582] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90103367 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Intra-ocular pressure, Goldmann-correlated right (UKB data field 5255) 57,066 European ancestry individuals NA NR [299582] 0 intraocular pressure measurement http://www.ebi.ac.uk/efo/EFO_0004695 GCST90103368 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Mood swings (UKB data field 1920) 71,215 European ancestry cases, 95,044 European ancestry controls NA NR [299582] 0 mood instability measurement http://www.ebi.ac.uk/efo/EFO_0008475 GCST90103369 Exome-wide sequencing 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Carnitine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90239991 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Decanoylcarnitine levels 2,733 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90239992 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Decenoylcarnitine levels 5,755 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 decenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021803 GCST90239993 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Decadienylcarnitine levels 5,757 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 decadienylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801231 GCST002961 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Dodecenoylcarnitine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 dodecenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021808 GCST90239995 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Tetradecenoylcarnitine levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 tetradecenoylcarnitine meaasurement http://www.ebi.ac.uk/efo/EFO_0021809 GCST90239996 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hydroxytetradecenoylcarnitine levels 1,825 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 hydroxytetradecenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801232 GCST90239997 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Tetradecadienylcarnitine levels 5,757 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 tetradecadienylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801233 GCST90239998 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Octadecenoylcarnitine levels 6,606 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 octadecenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801234 GCST90239999 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Octadecadienylcarnitine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 octadecadienylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801235 GCST90240000 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Acetylcarnitine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90240001 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Propionylcarnitine levels 1,588 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90240002 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hydroxypropionylcarnitine levels 1,589 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 hydroxypropionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801236 GCST90240003 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Glutaconylcarnitine levels 2,136 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 glutaconylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801237 GCST90240004 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Pimelylcarnitine levels 5,758 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 pimelylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801238 GCST90240005 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Octanoylcarnitine levels 2,732 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90240006 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Octenoylcarnitine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 octenoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801239 GCST90240007 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Nonaylcarnitine levels 4,562 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 nonaylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801240 GCST90240008 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Glutamine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90240009 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Glycine levels 7,475 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90240010 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hexose levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 hexose measurement http://www.ebi.ac.uk/efo/EFO_0007631 GCST002959 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Histidine levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90240012 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C16:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 lysophosphatidylcholine acyl C16:0 measurement http://www.ebi.ac.uk/efo/EFO_0801241 GCST90240013 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C16:1 levels 7,475 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST002965 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C17:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 lysophosphatidylcholine acyl C17:0 measurement http://www.ebi.ac.uk/efo/EFO_0801242 GCST90240015 Genome-wide genotyping array 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of E83 (disorders of mineral metabolism) (UKB data field 130821) 2,409 European ancestry cases, 168,348 European ancestry controls NA NR [299582] 0 mineral metabolism disease http://www.ebi.ac.uk/efo/EFO_0009556 GCST90103395 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of F17 (mental and behavioural disorders due to use of tobacco) (UKB data field 130869) 14,220 European ancestry cases, 156,537 European ancestry controls NA NR [299582] 0 mental or behavioural disorder http://www.ebi.ac.uk/efo/EFO_0000677 GCST90103396 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of G35 (multiple sclerosis) (UKB data field 131043) 806 European ancestry cases, 169,951 European ancestry controls NA NR [299582] 0 multiple sclerosis http://purl.obolibrary.org/obo/MONDO_0005301 GCST90103397 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of H18 (other disorders of cornea) (UKB data field 131155) 1,259 European ancestry cases, 169,498 European ancestry controls NA NR [299582] 0 corneal disease http://www.ebi.ac.uk/efo/EFO_0009464 GCST90103398 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of H20 (iridocyclitis) (UKB data field 131159) 971 European ancestry cases, 169,786 European ancestry controls NA NR [299582] 0 Iridocyclitis http://purl.obolibrary.org/obo/HP_0001094 GCST90103399 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of H36 (retinal disorders in diseases classified elsewhere) (UKB data field 131185) 1,205 European ancestry cases, 169,552 European ancestry controls NA NR [299582] 0 retinopathy http://www.ebi.ac.uk/efo/EFO_0003839 GCST90103400 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I10 (essential (primary) hypertension) (UKB data field 131287) 49,497 European ancestry cases, 121,260 European ancestry controls NA NR [299582] 0 essential hypertension http://purl.obolibrary.org/obo/MONDO_0001134 GCST90103401 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I12 (hypertensive renal disease) (UKB data field 131291) 618 European ancestry cases, 170,139 European ancestry controls NA NR [299582] 0 hypertensive nephropathy http://purl.obolibrary.org/obo/MONDO_0024633 GCST90103402 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I20 (angina pectoris) (UKB data field 131297) 10,617 European ancestry cases, 160,140 European ancestry controls NA NR [299582] 0 angina pectoris http://www.ebi.ac.uk/efo/EFO_0003913 GCST90103403 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I21 (acute myocardial infarction) (UKB data field 131299) 5,541 European ancestry cases, 165,216 European ancestry controls NA NR [299582] 0 myocardial infarction http://www.ebi.ac.uk/efo/EFO_0000612 GCST90103404 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I25 (chronic ischaemic heart disease) (UKB data field 131307) 14,175 European ancestry cases, 156,582 European ancestry controls NA NR [299582] 0 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90103405 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I35 (nonrheumatic aortic valve disorders) (UKB data field 131325) 2,181 European ancestry cases, 168,576 European ancestry controls NA NR [299582] 0 aortic valve disease http://www.ebi.ac.uk/efo/EFO_0009531 GCST90103406 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I50 (heart failure) (UKB data field 131355) 4,289 European ancestry cases, 166,468 European ancestry controls NA NR [299582] 0 heart failure http://www.ebi.ac.uk/efo/EFO_0003144 GCST90103407 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I80 (phlebitis and thrombophlebitis) (UKB data field 131397) 6,210 European ancestry cases, 164,547 European ancestry controls NA NR [299582] 0 Phlebitis http://www.ebi.ac.uk/efo/EFO_1001395 GCST90103408 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of I86 (varicose veins of other sites) (UKB data field 131409) 743 European ancestry cases, 170,014 European ancestry controls NA NR [299582] 0 Varicose veins http://purl.obolibrary.org/obo/HP_0002619 GCST90103409 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of J22 (unspecified acute lower respiratory infection) (UKB data field 131463) 21,743 European ancestry cases, 149,014 European ancestry controls NA NR [299582] 0 lower respiratory tract disease http://www.ebi.ac.uk/efo/EFO_0009433 GCST90103410 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of J33 (nasal polyp) (UKB data field 131471) 2,780 European ancestry cases, 167,977 European ancestry controls NA NR [299582] 0 Nasal Cavity Polyp http://www.ebi.ac.uk/efo/EFO_1000391 GCST90103411 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of J45 (asthma) (UKB data field 131495) 23,991 European ancestry cases, 146,766 European ancestry controls NA NR [299582] 0 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90103412 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of K70 (alcoholic liver disease) (UKB data field 131659) 595 European ancestry cases, 170,162 European ancestry controls NA NR [299582] 0 alcoholic liver disease http://www.ebi.ac.uk/efo/EFO_0008573 GCST90103413 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of K74 (fibrosis and cirrhosis of liver) (UKB data field 131667) 710 European ancestry cases, 170,047 European ancestry controls NA NR [299582] 0 cirrhosis of liver http://www.ebi.ac.uk/efo/EFO_0001422 GCST90103414 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of K76 (other diseases of liver) (UKB data field 131671) 4,151 European ancestry cases, 166,606 European ancestry controls NA NR [299582] 0 liver disease http://www.ebi.ac.uk/efo/EFO_0001421 GCST90103415 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of K90 (intestinal malabsorption) (UKB data field 131689) 1,724 European ancestry cases, 169,033 European ancestry controls NA NR [299582] 0 malabsorption syndrome http://www.ebi.ac.uk/efo/EFO_0009554 GCST90103416 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of L30 (other dermatitis) (UKB data field 131741) 17,277 European ancestry cases, 153,480 European ancestry controls NA NR [299582] 0 skin disease http://www.ebi.ac.uk/efo/EFO_0000701 GCST90103417 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of L40 (psoriasis) (UKB data field 131743) 5,210 European ancestry cases, 165,547 European ancestry controls NA NR [299582] 0 psoriasis http://www.ebi.ac.uk/efo/EFO_0000676 GCST90103418 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of L71 (rosacea) (UKB data field 131793) 2,109 European ancestry cases, 168,648 European ancestry controls NA NR [299582] 0 rosacea http://www.ebi.ac.uk/efo/EFO_1000760 GCST90103419 Exome-wide sequencing 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C34:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C34:2 measurement http://www.ebi.ac.uk/efo/EFO_0801286 GCST90240066 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C34:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C34:3 measurement http://www.ebi.ac.uk/efo/EFO_0801287 GCST90240067 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C36:0 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C36:0 measurement http://www.ebi.ac.uk/efo/EFO_0801288 GCST90240068 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C36:1 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C36:1 measurement http://www.ebi.ac.uk/efo/EFO_0801289 GCST90240069 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C36:2 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C36:2 measurement http://www.ebi.ac.uk/efo/EFO_0801290 GCST90240070 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C36:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C36:3 measurement http://www.ebi.ac.uk/efo/EFO_0801291 GCST90240071 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C36:4 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C36:4 measurement http://www.ebi.ac.uk/efo/EFO_0801292 GCST90240072 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Arginine levels 5,758 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90239990 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C36:5 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 phosphatidylcholine acyl-alkyl C36:5 measurement http://www.ebi.ac.uk/efo/EFO_0801293 GCST90240073 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C38:0 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C38:0 measurement http://www.ebi.ac.uk/efo/EFO_0801294 GCST90240074 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C38:1 levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C38:1 measurement http://www.ebi.ac.uk/efo/EFO_0801295 GCST90240075 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C38:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C38:2 measurement http://www.ebi.ac.uk/efo/EFO_0801296 GCST90240076 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C38:3 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C38:3 measurement http://www.ebi.ac.uk/efo/EFO_0801297 GCST90240077 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C38:4 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C38:4 measurement http://www.ebi.ac.uk/efo/EFO_0801298 GCST90240078 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C38:5 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C38:5 measurement http://www.ebi.ac.uk/efo/EFO_0801299 GCST90240079 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C40:1 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C40:1 measurement http://www.ebi.ac.uk/efo/EFO_0801301 GCST90240081 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C40:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C40:3 measurement http://www.ebi.ac.uk/efo/EFO_0801303 GCST90240083 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C40:6 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C40:6 measurement http://www.ebi.ac.uk/efo/EFO_0801306 GCST90240086 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C42:1 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C42:1 measurement http://www.ebi.ac.uk/efo/EFO_0801308 GCST90240088 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C18:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90240016 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C18:1 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90240017 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C18:2 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90240018 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C20:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 3 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90240019 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C20:4 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90240020 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C28:0 levels 6,602 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 lysophosphatidylcholine acyl C28:0 measurement http://www.ebi.ac.uk/efo/EFO_0801243 GCST90240021 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. lysoPhosphatidylcholine acyl C28:1 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 lysophosphatidylcholine acyl C28:1 measurement http://www.ebi.ac.uk/efo/EFO_0801244 GCST90240022 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Methionine levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90240023 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Ornithine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90240024 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C24:0 levels 3,821 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C24:0 measurement http://www.ebi.ac.uk/efo/EFO_0801245 GCST90240025 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C28:1 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C28:1 measurement http://www.ebi.ac.uk/efo/EFO_0801246 GCST90240026 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C30:0 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C30:0 measurement http://www.ebi.ac.uk/efo/EFO_0801247 GCST90240027 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C32:0 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C32:0 measurement http://www.ebi.ac.uk/efo/EFO_0801248 GCST90240028 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C32:1 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C32:1 measurement http://www.ebi.ac.uk/efo/EFO_0801249 GCST90240029 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C32:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C32:2 measurement http://www.ebi.ac.uk/efo/EFO_0801250 GCST90240030 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C32:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C32:3 measurement http://www.ebi.ac.uk/efo/EFO_0801251 GCST90240031 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C34:1 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C34:1 measurement http://www.ebi.ac.uk/efo/EFO_0801252 GCST90240032 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C34:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C34:2 measurement http://www.ebi.ac.uk/efo/EFO_0801253 GCST90240033 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C34:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C34:3 measurement http://www.ebi.ac.uk/efo/EFO_0801254 GCST90240034 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C34:4 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C34:4 measurement http://www.ebi.ac.uk/efo/EFO_0801255 GCST90240035 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C36:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C36:0 measurement http://www.ebi.ac.uk/efo/EFO_0801256 GCST90240036 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C36:1 levels 7,475 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C36:1 measurement http://www.ebi.ac.uk/efo/EFO_0801257 GCST90240037 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C36:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C36:2 measurement http://www.ebi.ac.uk/efo/EFO_0801258 GCST90240038 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C36:3 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C36:3 measurement http://www.ebi.ac.uk/efo/EFO_0801259 GCST90240039 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C36:4 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C36:4 measurement http://www.ebi.ac.uk/efo/EFO_0801260 GCST90240040 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C36:5 levels 7,474 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C36:5 measurement http://www.ebi.ac.uk/efo/EFO_0801261 GCST90240041 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C36:6 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C36:6 measurement http://www.ebi.ac.uk/efo/EFO_0801262 GCST90240042 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C38:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C38:0 measurement http://www.ebi.ac.uk/efo/EFO_0801263 GCST90240043 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C38:1 levels 1,497 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C38:1 measurement http://www.ebi.ac.uk/efo/EFO_0801264 GCST90240044 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C38:3 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C38:3 measurement http://www.ebi.ac.uk/efo/EFO_0801265 GCST90240045 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C38:4 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C38:4 measurement http://www.ebi.ac.uk/efo/EFO_0801266 GCST90240046 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C38:5 levels 7,475 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C38:5 measurement http://www.ebi.ac.uk/efo/EFO_0801267 GCST90240047 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C38:6 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C38:6 measurement http://www.ebi.ac.uk/efo/EFO_0801268 GCST90240048 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C40:1 levels 4,818 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C40:1 measurement http://www.ebi.ac.uk/efo/EFO_0801269 GCST90240049 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C40:2 levels 7,474 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C40:2 measurement http://www.ebi.ac.uk/efo/EFO_0801270 GCST90240050 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C40:3 levels 7,474 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C40:3 measurement http://www.ebi.ac.uk/efo/EFO_0801271 GCST90240051 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C40:4 levels 7,474 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C40:4 measurement http://www.ebi.ac.uk/efo/EFO_0801272 GCST90240052 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C40:5 levels 7,474 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C40:5 measurement http://www.ebi.ac.uk/efo/EFO_0801273 GCST90240053 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C40:6 levels 7,476 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C40:6 measurement http://www.ebi.ac.uk/efo/EFO_0801274 GCST90240054 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C42:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C42:0 measurement http://www.ebi.ac.uk/efo/EFO_0801275 GCST90240055 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C42:1 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C42:1 measurement http://www.ebi.ac.uk/efo/EFO_0801276 GCST90240056 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C42:2 levels 7,474 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine diacyl C42:2 measurement http://www.ebi.ac.uk/efo/EFO_0801277 GCST90240057 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C42:4 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C42:4 measurement http://www.ebi.ac.uk/efo/EFO_0801278 GCST90240058 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C42:5 levels 7,475 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C42:5 measurement http://www.ebi.ac.uk/efo/EFO_0801279 GCST90240059 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine diacyl C42:6 levels 6,601 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine diacyl C42:6 measurement http://www.ebi.ac.uk/efo/EFO_0801280 GCST90240060 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C30:0 levels 6,605 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C30:0 measurement http://www.ebi.ac.uk/efo/EFO_0801281 GCST90240061 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C32:1 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C32:1 measurement http://www.ebi.ac.uk/efo/EFO_0801282 GCST90240062 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C32:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C32:2 measurement http://www.ebi.ac.uk/efo/EFO_0801283 GCST90240063 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C34:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C34:0 measurement http://www.ebi.ac.uk/efo/EFO_0801284 GCST90240064 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C34:1 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C34:1 measurement http://www.ebi.ac.uk/efo/EFO_0801285 GCST90240065 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C38:6 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C38:6 measurement http://www.ebi.ac.uk/efo/EFO_0801300 GCST90240080 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C40:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C40:2 measurement http://www.ebi.ac.uk/efo/EFO_0801302 GCST90240082 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C40:4 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C40:4 measurement http://www.ebi.ac.uk/efo/EFO_0801304 GCST90240084 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C40:5 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C40:5 measurement http://www.ebi.ac.uk/efo/EFO_0801305 GCST90240085 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C42:0 levels 6,605 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C42:0 measurement http://www.ebi.ac.uk/efo/EFO_0801307 GCST90240087 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C42:2 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C42:2 measurement http://www.ebi.ac.uk/efo/EFO_0801309 GCST90240089 Genome-wide genotyping array 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of M06 (other rheumatoid arthritis) (UKB data field 131851) 3,877 European ancestry cases, 166,880 European ancestry controls NA NR [299582] 0 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90103420 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of M10 (gout) (UKB data field 131859) 6,209 European ancestry cases, 164,548 European ancestry controls NA NR [299582] 0 gout http://www.ebi.ac.uk/efo/EFO_0004274 GCST90103421 Exome-wide sequencing 2023-04-11 36779085 Fitzgerald T 2022-08-10 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36779085 CNest: A novel copy number association discovery method uncovers 862 new associations from 200,629 whole-exome sequence datasets in the UK Biobank. Source of report of M35 (other systemic involvement of connective tissue) (UKB data field 131901) 2,146 European ancestry cases, 168,611 European ancestry controls NA NR [299582] 0 connective tissue disease http://www.ebi.ac.uk/efo/EFO_1001986 GCST90103422 Exome-wide sequencing 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 7-methylguanine levels 6,091 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90243802 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phenylacetylglutamine levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90243803 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pro-hydroxy-pro levels 7,787 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90243804 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N2,n2-dimethylguanosine levels 5,228 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90243805 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cysteine-glutathione disulfide levels 1,997 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90243806 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Oleoylcarnitine levels 7,708 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90243807 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-arachidonoylglycerophosphoethanolamine levels 7,798 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 1-arachidonoylglycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0021077 GCST90243808 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13429 levels 6,344 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-13429 measurement http://www.ebi.ac.uk/efo/EFO_0021348 GCST90243809 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13431--nonanoylcarnitine levels 6,591 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-13431--nonanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021349 GCST90243810 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13435 levels 6,970 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-13435 measurement http://www.ebi.ac.uk/efo/EFO_0021350 GCST90243811 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13477 levels 5,952 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-13477 measurement http://www.ebi.ac.uk/efo/EFO_0021351 GCST90243812 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-palmitoylglycerophosphocholine levels 7,695 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-palmitoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021097 GCST90243813 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-oleoylglycerophosphocholine levels 7,524 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-oleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021096 GCST90243814 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-stearoylglycerophosphocholine levels 7,730 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-stearoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021098 GCST90243815 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-linoleoylglycerophosphocholine levels 6,894 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-linoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021095 GCST90243816 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13496 levels 7,656 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13496 measurement http://www.ebi.ac.uk/efo/EFO_0021352 GCST90243817 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-palmitoylglycerophosphoinositol levels 6,282 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-palmitoylglycerophosphoinositol measurement http://www.ebi.ac.uk/efo/EFO_0021091 GCST90243818 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Catechol sulfate levels 7,807 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90243819 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hydroquinone sulfate levels 451 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90243820 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13548 levels 6,022 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-13548 measurement http://www.ebi.ac.uk/efo/EFO_0021353 GCST90243821 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13549 levels 7,330 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13549 measurement http://www.ebi.ac.uk/efo/EFO_0021354 GCST90243822 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13553 levels 3,085 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13553 measurement http://www.ebi.ac.uk/efo/EFO_0021355 GCST90243823 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13619 levels 7,791 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13619 measurement http://www.ebi.ac.uk/efo/EFO_0021356 GCST90243824 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-methylbutyroylcarnitine levels 7,420 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-methylbutyroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021019 GCST90243825 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hydroxyisovaleroyl carnitine levels 5,588 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90243826 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glutaroyl carnitine levels 7,701 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 6 glutaroyl carnitine measurement http://www.ebi.ac.uk/efo/EFO_0021005 GCST90243827 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13658 levels 1,412 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13658 measurement http://www.ebi.ac.uk/efo/EFO_0021357 GCST90243828 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13671 levels 7,311 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-13671 measurement http://www.ebi.ac.uk/efo/EFO_0021358 GCST90243829 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-tetradecenoyl carnitine levels 6,998 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90243830 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-hydroxyhippurate levels 4,368 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90243831 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13741 levels 5,325 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13741 measurement http://www.ebi.ac.uk/efo/EFO_0021359 GCST90243832 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-myristoylglycerophosphocholine levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-myristoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021085 GCST90243833 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-oleoylglycerophosphoethanolamine levels 7,749 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-oleoylglycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0021087 GCST90243834 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-palmitoylglycerophosphoethanolamine levels 7,763 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 1-palmitoylglycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0021090 GCST90243835 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-3-hydroxyphenylpropionate levels 1,163 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-3-hydroxyphenylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0021007 GCST90243836 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Tetradecanedioate levels 6,046 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90243837 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-hydroxypalmitate levels 7,797 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90243838 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hexadecanedioate levels 6,887 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90243839 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Dihomo-linolenate 20:3n3 or n6 levels 7,805 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90243840 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13859 levels 7,002 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13859 measurement http://www.ebi.ac.uk/efo/EFO_0021360 GCST90243841 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Threitol levels 7,381 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 threitol measurement http://www.ebi.ac.uk/efo/EFO_0021031 GCST90243842 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14056 levels 7,259 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90243843 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14057 levels 4,716 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14057 measurement http://www.ebi.ac.uk/efo/EFO_0021362 GCST90243844 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14086 levels 2,686 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14086 measurement http://www.ebi.ac.uk/efo/EFO_0021363 GCST90243845 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Thymol sulfate levels 4,172 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90243846 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-acetaminophen sulfate levels 498 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 4-acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021156 GCST90243847 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-vinylphenol sulfate levels 7,483 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90243848 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-ethylphenylsulfate levels 6,012 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90243849 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. P-cresol sulfate levels 7,758 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90243850 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14189--leucylalanine levels 2,745 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-14189--leucylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021364 GCST90243851 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10395 levels 7,784 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-10395 measurement http://www.ebi.ac.uk/efo/EFO_0021213 GCST90243552 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10429 levels 6,807 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-10429 measurement http://www.ebi.ac.uk/efo/EFO_0021214 GCST90243553 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10500 levels 7,751 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-10500 measurement http://www.ebi.ac.uk/efo/EFO_0021215 GCST90243554 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10506 levels 7,710 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-10506 measurement http://www.ebi.ac.uk/efo/EFO_0021216 GCST90243555 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10510 levels 7,792 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-10510 measurement http://www.ebi.ac.uk/efo/EFO_0021217 GCST90243556 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-linoleoylglycerol 1-monolinolein levels 2,797 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 1-linoleoylglycerol 1-monolinolein measurement http://www.ebi.ac.uk/efo/EFO_0021108 GCST90243557 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Indoleacetate levels 7,618 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90243558 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hyodeoxycholate levels 6,025 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 hyodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010499 GCST90243559 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-indoxyl sulfate levels 7,787 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010502 GCST90243560 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N-acetylglycine levels 7,135 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90243561 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Bilirubin (z,z) levels 6,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90243562 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Creatine levels 7,822 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90243563 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Erythrose levels 7,263 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 erythrose measurement http://www.ebi.ac.uk/efo/EFO_0021026 GCST90243564 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycerol 2-phosphate levels 5,912 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycerol 2-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0021152 GCST90243565 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Threonate levels 7,782 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90243566 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10810 levels 7,232 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-10810 measurement http://www.ebi.ac.uk/efo/EFO_0021218 GCST90243567 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cysteine levels 7,692 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90243568 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pyroglutamylglycine levels 1,586 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pyroglutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021133 GCST90243569 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N-(2-furoyl)glycine levels 604 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 N-2-furoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021165 GCST90243570 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. DSGEGDFXAEGGGVR levels 5,371 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 DSGEGDFXAEGGGVR measurement http://www.ebi.ac.uk/efo/EFO_0021136 GCST90243571 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pyridoxate levels 7,703 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90243572 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Androsterone sulfate levels 7,785 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90243573 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90243574 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-(4-hydroxyphenyl)lactate levels 7,795 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90243575 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Acetylcarnitine levels 7,805 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90243576 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glutamine levels 7,821 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST002443 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Tryptophan levels 7,804 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90243403 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Histidine levels 7,804 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90243404 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Leucine levels 7,799 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90243405 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cholesterol levels 7,813 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90243406 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phenylalanine levels 7,803 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90243407 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Creatinine levels 7,810 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90243408 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Lactate levels 7,814 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90243409 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-hydroxybutyrate (bhba) levels 7,820 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90243410 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Caffeine levels 7,719 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90243411 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Arabinose levels 5,889 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 arabinose measurement http://www.ebi.ac.uk/efo/EFO_0021030 GCST90243412 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Fructose levels 7,781 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90243413 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Mannose levels 7,793 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90243414 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pyruvate levels 7,682 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90243415 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Uridine levels 7,800 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90243416 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Linoleate 18:2n6 levels 7,780 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 linoleate 18:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021510 GCST90243417 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Allantoin levels 5,705 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90243418 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Arachidonate (20:4n6) levels 7,816 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90243419 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Deoxycholate levels 5,194 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90243420 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Margarate 17:0 levels 7,796 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90243421 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Inosine levels 2,675 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90243422 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Isoleucine levels 7,801 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90243423 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Threonine levels 6,020 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90243424 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Tyrosine levels 7,807 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90243425 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Lysine levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90243426 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14205--alpha-glutamyltyrosine levels 1,789 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-14205--alpha-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021365 GCST90243852 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14208--phenylalanylserine levels 2,455 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-14208--phenylalanylserine measurement http://www.ebi.ac.uk/efo/EFO_0021366 GCST90243853 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14304--leucylalanine levels 2,434 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-14304--leucylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021367 GCST90243854 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14374 levels 7,627 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14374 measurement http://www.ebi.ac.uk/efo/EFO_0021368 GCST90243855 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14450--phenylalanylleucine levels 2,555 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14450--phenylalanylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021369 GCST90243856 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14473 levels 6,884 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-14473 measurement http://www.ebi.ac.uk/efo/EFO_0021370 GCST90243857 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14541 levels 1,941 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14541 measurement http://www.ebi.ac.uk/efo/EFO_0021371 GCST90243858 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14588 levels 7,777 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14588 measurement http://www.ebi.ac.uk/efo/EFO_0021372 GCST90243859 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14625 levels 7,511 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-14625 measurement http://www.ebi.ac.uk/efo/EFO_0021373 GCST90243860 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14626 levels 6,904 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-14626 measurement http://www.ebi.ac.uk/efo/EFO_0021374 GCST90243861 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14632 levels 1,703 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14632 measurement http://www.ebi.ac.uk/efo/EFO_0021375 GCST90243862 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14658 levels 3,533 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14658 measurement http://www.ebi.ac.uk/efo/EFO_0021376 GCST90243863 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14662 levels 4,212 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14662 measurement http://www.ebi.ac.uk/efo/EFO_0021377 GCST90243864 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14745 levels 5,602 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14745 measurement http://www.ebi.ac.uk/efo/EFO_0021378 GCST90243865 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylglutamate levels 931 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90243866 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Octadecanedioate levels 7,300 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90243867 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Leucylleucine levels 3,386 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 leucylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021130 GCST90243868 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 7,784 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 7-alpha-hydroxy-3-oxo-4-cholestenoate 7-Hoca measurement http://www.ebi.ac.uk/efo/EFO_0021116 GCST90243869 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N-Butyl Oleate levels 4,542 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 n-Butyl Oleate measurement http://www.ebi.ac.uk/efo/EFO_0021058 GCST90243870 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Dimethylarginine (sdma + adma) levels 7,347 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 serum dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0005418 GCST90243871 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Taurolithocholate 3-sulfate levels 6,904 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90243872 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-14977--vanillin levels 1,789 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-14977--vanillin measurement http://www.ebi.ac.uk/efo/EFO_0021379 GCST90243873 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Succinylcarnitine levels 6,948 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 4 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90243874 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Tryptophan betaine levels 7,439 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90243875 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cycloleu-pro levels 4,833 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 cycloleu-pro measurement http://www.ebi.ac.uk/efo/EFO_0021128 GCST90243876 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1,3,7-trimethylurate levels 796 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90243777 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Isovalerylcarnitine levels 7,789 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 isovalerylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020019 GCST90243778 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Stearoylcarnitine levels 7,183 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90243779 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-stearoylglycerophosphoethanolamine levels 7,369 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 1-stearoylglycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0021093 GCST90243780 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-linoleoylglycerophosphocholine levels 7,795 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-linoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021083 GCST90243781 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Bradykinin, des-arg 9 levels 4,570 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 bradykinin, des-arg 9 measurement http://www.ebi.ac.uk/efo/EFO_0021146 GCST90243782 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12771 levels 4,734 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12771 measurement http://www.ebi.ac.uk/efo/EFO_0021332 GCST90243783 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12776 levels 7,764 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12776 measurement http://www.ebi.ac.uk/efo/EFO_0021333 GCST90243784 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylisoleucine levels 5,522 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90243785 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12786 levels 6,566 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12786 measurement http://www.ebi.ac.uk/efo/EFO_0021334 GCST90243786 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12798 levels 7,552 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90243787 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12816 levels 4,524 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12816 measurement http://www.ebi.ac.uk/efo/EFO_0021336 GCST90243788 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12830 levels 3,415 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12830 measurement http://www.ebi.ac.uk/efo/EFO_0021337 GCST90243789 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12833 levels 243 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12833 measurement http://www.ebi.ac.uk/efo/EFO_0021338 GCST90243790 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12844 levels 7,768 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90243791 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12847 levels 4,036 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90243792 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12850 levels 6,251 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12850 measurement http://www.ebi.ac.uk/efo/EFO_0021341 GCST90243793 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Laurylcarnitine levels 5,170 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90243794 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12851 levels 4,808 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12851 measurement http://www.ebi.ac.uk/efo/EFO_0021342 GCST90243795 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12855 levels 5,120 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12855 measurement http://www.ebi.ac.uk/efo/EFO_0021343 GCST90243796 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12990--docosapentaenoic acid n6-DPA levels 2,581 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12990--docosapentaenoic acid n6-DPA measurement http://www.ebi.ac.uk/efo/EFO_0021344 GCST90243797 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Isovalerate levels 7,080 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 isovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021051 GCST90243798 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13069 levels 6,770 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13069 measurement http://www.ebi.ac.uk/efo/EFO_0021345 GCST90243799 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13183--stearamide levels 2,503 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13183--stearamide measurement http://www.ebi.ac.uk/efo/EFO_0021346 GCST90243800 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13215 levels 6,305 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-13215 measurement http://www.ebi.ac.uk/efo/EFO_0021347 GCST90243801 Genome-wide genotyping array 2022-12-16 35653140 Fasching PA 2022-06-02 Clin Cancer Res www.ncbi.nlm.nih.gov/pubmed/35653140 Identification of Two Genetic Loci Associated with Leukopenia after Chemotherapy in Breast Cancer Patients. Adverse response to chemotherapy in breast cancer (grade 3/4 neutropenic or leukopenic events) 1,679 European ancestry cases with events, 1,643 European ancestry cases without events NA Illumina [8860000] (imputed) 2 neutropenia, leukopenia, chemotherapy-induced cytotoxicity measurement http://purl.obolibrary.org/obo/MONDO_0001475, http://www.ebi.ac.uk/efo/EFO_0004233, http://www.ebi.ac.uk/efo/EFO_0010978 GCST90244025 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylputrescine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90257538 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylserine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90257539 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetyltryptophan levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800018 GCST90257540 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-alpha-acetylarginine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90257541 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Nicotinuric acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90257542 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-lauroylglycine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-lauroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0801188 GCST90257543 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-methylproline levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90257544 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Leucine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90257545 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Oleoyl glycine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 oleoyl glycine measurement http://www.ebi.ac.uk/efo/EFO_0801207 GCST90257546 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. O-methyladenosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90257547 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pantothenate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90257548 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phenylacetylglutamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90257549 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pro-gly levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 pro-gly measurement http://www.ebi.ac.uk/efo/EFO_0801216 GCST90257550 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pseudouridine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90257551 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pyridoxine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST90257552 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Isoleucine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90257553 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Ribothymidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90257554 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sphinganine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90257555 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Trigonelline levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90257556 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Urate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90257557 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Urocanic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 Urocanic acid (RG) measurement http://www.ebi.ac.uk/efo/EFO_0021676 GCST90257558 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Valsartan levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 valsartan measurement http://www.ebi.ac.uk/efo/EFO_0801224 GCST90257559 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phenylalanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90257560 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90257561 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90257562 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C20:0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801125 GCST90257588 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90257589 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Proline levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90257590 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C30:0 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C30:0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0801129 GCST90257591 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:2 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90257592 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:4 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 34:4 measurement http://www.ebi.ac.uk/efo/EFO_0010378 GCST90257593 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0010377 GCST90257594 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010376 GCST90257595 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010380 GCST90257596 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:3 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801134 GCST90257597 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 C36:5 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801141 GCST90257598 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:7 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801148 GCST90257599 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801132 GCST90257600 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hydroxyproline levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0010498 GCST90257601 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801130 GCST90257602 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801140 GCST90257603 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801136 GCST90257604 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 C38:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801146 GCST90257605 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801143 GCST90257606 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:6 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C40:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801151 GCST90257607 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801135 GCST90257608 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:2 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801133 GCST90257609 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801142 GCST90257610 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801138 GCST90257611 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Ornithine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90257612 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90257563 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90257564 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90257565 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90257566 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90257567 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tyrosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90257568 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:5 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90257569 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90257570 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:3 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90257571 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:1 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90257572 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90257573 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:5 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90257574 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:4 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90257575 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:0 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90257576 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Lysophosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257577 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine plasmalogen-A levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257578 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tryptophan levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90257579 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine plasmalogen-B levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257580 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90257581 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C18:3 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801124 GCST90257582 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90257583 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90257584 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90257585 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90257586 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:1 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C20:1 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801127 GCST90257587 Genome-wide genotyping array 2023-08-18 37108169 Gelemanovic A 2023-04-10 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37108169 Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. Meningitis 7 Vis (founder/genetic isolate) cases, 16 Korculan (founder/genetic isolate) cases, 7 Split cases, 953 Vis (founder/genetic isolate) controls, 2,682 Korculan (founder/genetic isolate) controls, 959 Split controls NA Illumina [11400586] (imputed) 8 meningitis http://purl.obolibrary.org/obo/MONDO_0021108 GCST90276150 Genome-wide genotyping array 2023-08-18 37108169 Gelemanovic A 2023-04-10 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37108169 Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. Pneumonia 105 Vis (founder/genetic isolate) cases, 235 Korculan (founder/genetic isolate) cases, 27 Split cases, 855 Vis (founder/genetic isolate) controls, 2,463 Korculan (founder/genetic isolate) controls, 939 Split controls NA Illumina [11400586] (imputed) 1 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90276151 Genome-wide genotyping array 2023-08-18 37108169 Gelemanovic A 2023-04-10 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37108169 Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. Systemic infections 26 Vis (founder/genetic isolate) cases, 36 Korculan (founder/genetic isolate) cases, 25 Split cases, 934 Vis (founder/genetic isolate) controls, 2,662 Korculan (founder/genetic isolate) controls, 941 Split controls NA Illumina [11400586] (imputed) 7 infection http://www.ebi.ac.uk/efo/EFO_0000544 GCST90276152 Genome-wide genotyping array 2023-08-18 37108169 Gelemanovic A 2023-04-10 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37108169 Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. Tuberculosis 12 Vis (founder/genetic isolate) cases, 16 Korculan (founder/genetic isolate) cases, 6 Split cases, 948 Vis (founder/genetic isolate) controls, 2,682 Korculan (founder/genetic isolate) controls, 960 Split controls NA Illumina [11400586] (imputed) 7 tuberculosis http://purl.obolibrary.org/obo/MONDO_0018076 GCST90276153 Genome-wide genotyping array 2023-08-18 37108169 Gelemanovic A 2023-04-10 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37108169 Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. Frequency of common cold infection 244 Vis (founder/genetic isolate) individuals, 771 Korculan (founder/genetic isolate) individuals NA Illumina [11400586] (imputed) 9 susceptibility to common cold measurement http://www.ebi.ac.uk/efo/EFO_0008417 GCST90276154 Genome-wide genotyping array 2023-08-18 37108169 Gelemanovic A 2023-04-10 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37108169 Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. Frequency of influenza infection 197 Vis (founder/genetic isolate) individuals, 655 Korculan (founder/genetic isolate) individuals NA Illumina [11400586] (imputed) 8 susceptibility to influenza measurement http://www.ebi.ac.uk/efo/EFO_0803537 GCST90276155 Genome-wide genotyping array 2023-08-18 37108169 Gelemanovic A 2023-04-10 Int J Mol Sci www.ncbi.nlm.nih.gov/pubmed/37108169 Genome-Wide Meta-Analysis Identifies Multiple Novel Rare Variants to Predict Common Human Infectious Diseases Risk. Hepatitis 26 Vis (founder/genetic isolate) cases, 30 Korculan (founder/genetic isolate) cases, 20 Split cases, 934 Vis (founder/genetic isolate) controls, 2,668 Korculan (founder/genetic isolate) controls, 946 Split controls NA Illumina [11400586] (imputed) 6 Hepatitis http://purl.obolibrary.org/obo/HP_0012115 GCST90276149 Genome-wide genotyping array 2023-01-09 35884923 Lee SB 2022-07-06 Biomedicines www.ncbi.nlm.nih.gov/pubmed/35884923 Dyslipidaemia-Genotype Interactions with Nutrient Intake and Cerebro-Cardiovascular Disease. Total cholesterol levels 58,701 Korean ancestry individuals NA Affymetrix [7975321] (imputed) 183 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90134518 Genome-wide genotyping array 2023-01-09 35884923 Lee SB 2022-07-06 Biomedicines www.ncbi.nlm.nih.gov/pubmed/35884923 Dyslipidaemia-Genotype Interactions with Nutrient Intake and Cerebro-Cardiovascular Disease. HDL cholesterol levels 58,701 Korean ancestry individuals NA Affymetrix [7975321] (imputed) 218 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90134519 Genome-wide genotyping array 2023-01-09 35884923 Lee SB 2022-07-06 Biomedicines www.ncbi.nlm.nih.gov/pubmed/35884923 Dyslipidaemia-Genotype Interactions with Nutrient Intake and Cerebro-Cardiovascular Disease. LDL cholesterol levels 58,701 Korean ancestry individuals NA Affymetrix [7975321] (imputed) 161 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90134520 Genome-wide genotyping array 2023-01-09 35884923 Lee SB 2022-07-06 Biomedicines www.ncbi.nlm.nih.gov/pubmed/35884923 Dyslipidaemia-Genotype Interactions with Nutrient Intake and Cerebro-Cardiovascular Disease. Triglyceride levels 58,701 Korean ancestry individuals NA Affymetrix [7975321] (imputed) 130 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90134521 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-07765 levels 2,170 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90243602 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11247 levels 7,403 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11247 measurement http://www.ebi.ac.uk/efo/EFO_0021220 GCST90243603 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11261 levels 7,771 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-11261 measurement http://www.ebi.ac.uk/efo/EFO_0021221 GCST90243604 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Bilirubin (E,E) levels 7,748 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90243605 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-02249 levels 7,818 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-02249 measurement http://www.ebi.ac.uk/efo/EFO_0021182 GCST90243606 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Heme levels 6,380 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 heme measurement http://www.ebi.ac.uk/efo/EFO_0800158 GCST90243607 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11299 levels 7,347 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90243608 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11315 levels 7,785 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90243609 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11317 levels 7,811 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11317 measurement http://www.ebi.ac.uk/efo/EFO_0021224 GCST90243610 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-linoleoylglycerophosphoethanolamine levels 7,817 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 1-linoleoylglycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0021084 GCST90243611 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11327 levels 7,671 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11327 measurement http://www.ebi.ac.uk/efo/EFO_0021225 GCST90243612 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11334 levels 5,462 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11334 measurement http://www.ebi.ac.uk/efo/EFO_0021226 GCST90243613 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-dehydrocarnitine levels 7,809 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 3-dehydrocarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021037 GCST90243614 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pyroglutamine levels 7,800 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 pyroglutamine measurement http://www.ebi.ac.uk/efo/EFO_0005408 GCST90243615 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. C-glycosyltryptophan levels 7,786 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90243616 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11374 levels 2,609 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11374 measurement http://www.ebi.ac.uk/efo/EFO_0021227 GCST90243617 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11381 levels 7,753 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90243618 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-03056--N-[3- 2-Oxopyrrolidin-1-yl propyl]acetamide levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 4 X-03056--N-[3- 2-Oxopyrrolidin-1-yl propyl]acetamide measurement http://www.ebi.ac.uk/efo/EFO_0021186 GCST90243619 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11412 levels 6,935 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11412 measurement http://www.ebi.ac.uk/efo/EFO_0021229 GCST90243620 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-01911 levels 6,360 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-01911 measurement http://www.ebi.ac.uk/efo/EFO_0021181 GCST90243621 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11422--xanthine levels 6,346 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11422--xanthine measurement http://www.ebi.ac.uk/efo/EFO_0021230 GCST90243622 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. O-sulfo-l-tyrosine levels 7,765 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11423--O-sulfo-L-tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021231 GCST90243623 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-09789 levels 7,805 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-09789 measurement http://www.ebi.ac.uk/efo/EFO_0021211 GCST90243624 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11437 levels 6,782 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11437 measurement http://www.ebi.ac.uk/efo/EFO_0021232 GCST90243625 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11438 levels 7,084 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11438 measurement http://www.ebi.ac.uk/efo/EFO_0021233 GCST90243626 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Kynurenine levels 7,816 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90243477 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Mannitol levels 5,917 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 mannitol measurement http://www.ebi.ac.uk/efo/EFO_0021027 GCST90243478 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycerol 3-phosphate levels 7,781 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90243479 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Acetylphosphate levels 7,789 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 acetylphosphate measurement http://www.ebi.ac.uk/efo/EFO_0021035 GCST90243480 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Carnitine levels 7,797 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 4 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90243481 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Choline levels 7,750 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90243482 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N-acetylornithine levels 7,574 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 GCST90243483 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N1-methyladenosine levels 7,813 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90243484 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-methyl-2-oxovalerate levels 7,779 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90243485 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-methylhistidine levels 5,885 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90243486 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-phenylpropionate hydrocinnamate levels 6,182 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90243487 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hippurate levels 7,806 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90243488 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Benzoate levels 7,756 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90243489 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phenylacetate levels 4,754 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90243490 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycerophosphorylcholine GPC levels 7,156 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90243491 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Aspartate levels 7,721 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90243492 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-04357 levels 7,502 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-04357 measurement http://www.ebi.ac.uk/efo/EFO_0021189 GCST90243493 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-04494 levels 5,007 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-04494 measurement http://www.ebi.ac.uk/efo/EFO_0021190 GCST90243494 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-04495 levels 7,490 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-04495 measurement http://www.ebi.ac.uk/efo/EFO_0021191 GCST90243495 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-04498 levels 7,160 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-04498 measurement http://www.ebi.ac.uk/efo/EFO_0021192 GCST90243496 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-04499--3,4-dihydroxybutyrate levels 6,948 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-04499--3,4-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021193 GCST90243497 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-04500 levels 3,647 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-04500 measurement http://www.ebi.ac.uk/efo/EFO_0021194 GCST90243498 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Ibuprofen levels 1,976 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 ibuprofen measurement http://www.ebi.ac.uk/efo/EFO_0021158 GCST90243499 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Dihomo-linoleate 20:2n6 levels 7,800 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90243500 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-18601 levels 7,663 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-18601 measurement http://www.ebi.ac.uk/efo/EFO_0021380 GCST90243501 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12007 levels 1,362 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90243677 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12013 levels 1,948 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90243678 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylmethionine levels 2,240 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90243679 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylthreonine levels 4,016 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90243680 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12029 levels 7,564 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12029 measurement http://www.ebi.ac.uk/efo/EFO_0021278 GCST90243681 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Salicyluric glucuronide levels 832 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 salicyluric glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0021162 GCST90243682 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12038 levels 7,758 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12038 measurement http://www.ebi.ac.uk/efo/EFO_0021279 GCST90243683 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12039 levels 5,461 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12039 measurement http://www.ebi.ac.uk/efo/EFO_0021280 GCST90243684 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12040 levels 559 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12040 measurement http://www.ebi.ac.uk/efo/EFO_0021281 GCST90243685 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12056 levels 4,130 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12056 measurement http://www.ebi.ac.uk/efo/EFO_0021282 GCST90243686 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12063 levels 7,197 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-12063 measurement http://www.ebi.ac.uk/efo/EFO_0021283 GCST90243687 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-tocopherol levels 6,226 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007899 GCST90243688 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylphenylalanine levels 7,753 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021142 GCST90243689 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. P-acetamidophenylglucuronide levels 1,494 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 p-acetamidophenylglucuronide measurement http://www.ebi.ac.uk/efo/EFO_0021160 GCST90243690 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Isobutyrylcarnitine levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90243691 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pseudouridine levels 7,785 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90243692 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Valerate levels 4,102 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 valerate measurement http://www.ebi.ac.uk/efo/EFO_0021112 GCST90243693 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Palmitoleate 16:1n7 levels 7,776 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90243694 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Alpha-ketoglutarate levels 6,130 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90243695 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Erythronate levels 7,752 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90243696 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Lathosterol levels 5,457 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 lathosterol measurement http://www.ebi.ac.uk/efo/EFO_0021121 GCST90243697 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12092 levels 7,500 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12092 measurement http://www.ebi.ac.uk/efo/EFO_0021284 GCST90243698 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12093 levels 2,854 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-12093 measurement http://www.ebi.ac.uk/efo/EFO_0021285 GCST90243699 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12094 levels 7,467 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12094 measurement http://www.ebi.ac.uk/efo/EFO_0021286 GCST90243700 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12095--N1-methyl-3-pyridone-4-carboxamide levels 7,711 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12095--N1-methyl-3-pyridone-4-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0021287 GCST90243701 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-hydroxystearate levels 7,763 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90243502 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Paraxanthine levels 7,504 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90243503 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-hydroxyhippurate salicylurate levels 2,592 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90243504 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-05426 levels 6,357 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-05426 measurement http://www.ebi.ac.uk/efo/EFO_0021195 GCST90243505 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Quinate levels 6,265 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90243506 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Indolelactate levels 7,378 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90243507 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycylvaline levels 2,108 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021129 GCST90243508 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylleucine levels 7,802 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90243509 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Theobromine levels 7,768 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90243510 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Theophylline levels 7,393 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90243511 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Eicosapentaenoate EPA; 20:5n3 levels 7,816 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 eicosapentaenoate EPA; 20:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021049 GCST90243512 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Estrone 3-sulfate levels 957 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 estrone conjugate measurement http://www.ebi.ac.uk/efo/EFO_0007971 GCST90243513 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycocholate levels 5,995 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90243514 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycodeoxycholate levels 1,477 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90243515 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Taurochenodeoxycholate levels 5,716 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90243516 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Taurocholate levels 4,032 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90243517 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-05907 levels 7,734 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-05907 measurement http://www.ebi.ac.uk/efo/EFO_0021196 GCST90243518 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Docosahexaenoate DHA; 22:6n3 levels 7,818 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 docosahexaenoate DHA; 22:6n3 measurement http://www.ebi.ac.uk/efo/EFO_0021047 GCST90243519 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-stearoylglycerophosphoinositol levels 7,694 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-stearoylglycerophosphoinositol measurement http://www.ebi.ac.uk/efo/EFO_0021094 GCST90243520 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-06226 levels 7,623 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-06226 measurement http://www.ebi.ac.uk/efo/EFO_0021198 GCST90243521 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-06246 levels 7,358 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-06246 measurement http://www.ebi.ac.uk/efo/EFO_0021199 GCST90243522 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-06267 levels 7,075 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-06267 measurement http://www.ebi.ac.uk/efo/EFO_0021200 GCST90243523 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-06307 levels 6,774 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-06307 measurement http://www.ebi.ac.uk/efo/EFO_0021201 GCST90243524 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-06350 levels 5,161 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-06350 measurement http://www.ebi.ac.uk/efo/EFO_0021202 GCST90243525 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-06351 levels 4,791 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-06351 measurement http://www.ebi.ac.uk/efo/EFO_0021203 GCST90243526 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Homostachydrine levels 3,003 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90243652 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. ADSGEGDFXAEGGGVR levels 5,588 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 ADSGEGDFXAEGGGVR measurement http://www.ebi.ac.uk/efo/EFO_0021135 GCST90243653 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11786--methylcysteine levels 2,811 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11786--methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0021257 GCST90243654 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11787 levels 7,811 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90243655 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11792 levels 2,442 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11792 measurement http://www.ebi.ac.uk/efo/EFO_0021259 GCST90243656 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11793--oxidized bilirubin levels 7,611 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11793--oxidized bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0021260 GCST90243657 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11795 levels 7,763 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90243658 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11799 levels 5,038 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11799 measurement http://www.ebi.ac.uk/efo/EFO_0021262 GCST90243659 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11805 levels 2,814 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11805 measurement http://www.ebi.ac.uk/efo/EFO_0021263 GCST90243660 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11818 levels 6,790 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11818 measurement http://www.ebi.ac.uk/efo/EFO_0021264 GCST90243661 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11820 levels 7,710 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11820 measurement http://www.ebi.ac.uk/efo/EFO_0021265 GCST90243662 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-hydroxyacetaminophen sulfate levels 1,688 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-hydroxyacetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021153 GCST90243663 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-methoxyacetaminophen sulfate levels 1,086 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-methoxyacetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021154 GCST90243664 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11843 levels 3,938 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90243665 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11845 levels 2,741 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11845 measurement http://www.ebi.ac.uk/efo/EFO_0021267 GCST90243666 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11847 levels 6,059 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90243667 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11849 levels 5,350 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90243668 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11850 levels 4,868 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90243669 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11852 levels 2,974 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90243670 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11858 levels 3,427 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90243671 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11859 levels 2,721 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11859 measurement http://www.ebi.ac.uk/efo/EFO_0021273 GCST90243672 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11876 levels 4,965 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11876 measurement http://www.ebi.ac.uk/efo/EFO_0021274 GCST90243673 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-arachidonoylglycerophosphocholine levels 7,507 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 1-arachidonoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021076 GCST90243674 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-palmitoleoylglycerophosphocholine levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-palmitoleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021088 GCST90243675 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11905 levels 4,761 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11905 measurement http://www.ebi.ac.uk/efo/EFO_0021275 GCST90243676 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12100--hydroxytryptophan levels 7,499 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12100--hydroxytryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021288 GCST90243702 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12116 levels 3,039 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12116 measurement http://www.ebi.ac.uk/efo/EFO_0021289 GCST90243703 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Eicosenoate 20:1n9 or 11 levels 7,799 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 eicosenoate 20:1n9 or 11 measurement http://www.ebi.ac.uk/efo/EFO_0021065 GCST90243704 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12188 levels 832 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12188 measurement http://www.ebi.ac.uk/efo/EFO_0021290 GCST90243705 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12189 levels 481 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12189 measurement http://www.ebi.ac.uk/efo/EFO_0021291 GCST90243706 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12206 levels 2,795 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12206 measurement http://www.ebi.ac.uk/efo/EFO_0021292 GCST90243707 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12212 levels 4,566 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12212 measurement http://www.ebi.ac.uk/efo/EFO_0021293 GCST90243708 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12216 levels 5,369 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90243709 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12217 levels 6,469 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12217 measurement http://www.ebi.ac.uk/efo/EFO_0021295 GCST90243710 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12230 levels 5,649 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12230 measurement http://www.ebi.ac.uk/efo/EFO_0021296 GCST90243711 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12231 levels 5,111 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12231 measurement http://www.ebi.ac.uk/efo/EFO_0021297 GCST90243712 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12236 levels 1,924 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12236 measurement http://www.ebi.ac.uk/efo/EFO_0021298 GCST90243713 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12244--N-acetylcarnosine levels 6,608 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 4 X-12244--N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0021299 GCST90243714 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12253 levels 6,004 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12253 measurement http://www.ebi.ac.uk/efo/EFO_0021300 GCST90243715 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12261 levels 1,050 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12261 measurement http://www.ebi.ac.uk/efo/EFO_0021301 GCST90243716 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12329 levels 867 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12329 measurement http://www.ebi.ac.uk/efo/EFO_0021302 GCST90243717 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10346 levels 4,207 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-10346 measurement http://www.ebi.ac.uk/efo/EFO_0021212 GCST90243718 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. ADpSGEGDFXAEGGGVR levels 3,939 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 ADpSGEGDFXAEGGGVR measurement http://www.ebi.ac.uk/efo/EFO_0021134 GCST90243719 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-eicosatrienoylglycerophosphocholine levels 7,809 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 1-eicosatrienoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021081 GCST90243720 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-docosahexaenoylglycerophosphocholine levels 7,798 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-docosahexaenoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021079 GCST90243721 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12405 levels 6,676 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12405 measurement http://www.ebi.ac.uk/efo/EFO_0021303 GCST90243722 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12407 levels 2,814 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90243723 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12428 levels 1,439 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12428 measurement http://www.ebi.ac.uk/efo/EFO_0021305 GCST90243724 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-eicosadienoylglycerophosphocholine levels 6,892 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-eicosadienoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021080 GCST90243725 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12435 levels 231 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12435 measurement http://www.ebi.ac.uk/efo/EFO_0021306 GCST90243726 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12544 levels 5,893 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12544 measurement http://www.ebi.ac.uk/efo/EFO_0021315 GCST90243752 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12556 levels 7,483 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-12556 measurement http://www.ebi.ac.uk/efo/EFO_0021316 GCST90243753 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-arachidonoylglycerophosphoinositol levels 7,797 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 1-arachidonoylglycerophosphoinositol measurement http://www.ebi.ac.uk/efo/EFO_0021078 GCST90243754 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12627 levels 7,419 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12627 measurement http://www.ebi.ac.uk/efo/EFO_0021317 GCST90243755 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12644 levels 7,795 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12644 measurement http://www.ebi.ac.uk/efo/EFO_0021318 GCST90243756 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12645 levels 5,254 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12645 measurement http://www.ebi.ac.uk/efo/EFO_0021319 GCST90243757 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Asparagine levels 7,761 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90243758 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12680 levels 2,311 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90243759 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12696 levels 7,409 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12696 measurement http://www.ebi.ac.uk/efo/EFO_0021321 GCST90243760 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12704 levels 1,813 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12704 measurement http://www.ebi.ac.uk/efo/EFO_0021322 GCST90243761 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12712 levels 260 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12712 measurement http://www.ebi.ac.uk/efo/EFO_0021323 GCST90243762 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12717 levels 1,632 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12717 measurement http://www.ebi.ac.uk/efo/EFO_0021324 GCST90243763 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12719 levels 1,539 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12719 measurement http://www.ebi.ac.uk/efo/EFO_0021325 GCST90243764 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12726 levels 5,495 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12726 measurement http://www.ebi.ac.uk/efo/EFO_0021326 GCST90243765 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12728 levels 537 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12728 measurement http://www.ebi.ac.uk/efo/EFO_0021327 GCST90243766 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12729 levels 1,753 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90243767 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12734 levels 5,616 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12734 measurement http://www.ebi.ac.uk/efo/EFO_0021329 GCST90243768 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12740 levels 3,731 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90243769 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12749 levels 7,178 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12749 measurement http://www.ebi.ac.uk/efo/EFO_0021331 GCST90243770 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-(cystein-S-yl)acetaminophen levels 1,024 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-cystein-S-ylacetaminophen measurement http://www.ebi.ac.uk/efo/EFO_0021155 GCST90243771 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Stachydrine levels 6,745 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90243772 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-methylxanthine levels 5,504 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90243773 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 7-methylxanthine levels 5,901 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90243774 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-methylurate levels 5,520 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90243775 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1,7-dimethylurate levels 6,057 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90243776 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11440 levels 7,686 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11440 measurement http://www.ebi.ac.uk/efo/EFO_0021234 GCST90243627 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11441 levels 7,072 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11441 measurement http://www.ebi.ac.uk/efo/EFO_0021235 GCST90243628 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11442 levels 7,142 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11442 measurement http://www.ebi.ac.uk/efo/EFO_0021236 GCST90243629 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11444 levels 7,758 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90243630 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11445--5-alpha-pregnan-3beta,20alpha-disulfate levels 2,570 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11445--5-alpha-pregnan-3beta,20alpha-disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021238 GCST90243631 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11452 levels 6,519 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11452 measurement http://www.ebi.ac.uk/efo/EFO_0021239 GCST90243632 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11469 levels 7,779 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-11469 measurement http://www.ebi.ac.uk/efo/EFO_0021240 GCST90243633 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11470 levels 7,271 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90243634 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11478 levels 6,593 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90243635 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11483 levels 4,608 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90243636 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11485 levels 4,544 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11485 measurement http://www.ebi.ac.uk/efo/EFO_0021244 GCST90243637 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11491 levels 6,584 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11491 measurement http://www.ebi.ac.uk/efo/EFO_0021245 GCST90243638 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11497 levels 7,481 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11497 measurement http://www.ebi.ac.uk/efo/EFO_0021246 GCST90243639 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. HWESASXX levels 7,700 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 HWESASXX measurement http://www.ebi.ac.uk/efo/EFO_0021147 GCST90243640 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11521 levels 7,193 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11521 measurement http://www.ebi.ac.uk/efo/EFO_0021247 GCST90243641 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11529 levels 6,664 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11529 measurement http://www.ebi.ac.uk/efo/EFO_0021248 GCST90243642 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11530 levels 7,409 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11530 measurement http://www.ebi.ac.uk/efo/EFO_0021249 GCST90243643 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11537 levels 2,719 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11537 measurement http://www.ebi.ac.uk/efo/EFO_0021250 GCST90243644 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11538 levels 7,804 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11538 measurement http://www.ebi.ac.uk/efo/EFO_0021251 GCST90243645 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11540 levels 2,688 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11540 measurement http://www.ebi.ac.uk/efo/EFO_0021252 GCST90243646 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11546 levels 2,015 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11546 measurement http://www.ebi.ac.uk/efo/EFO_0021253 GCST90243647 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11550 levels 7,776 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11550 measurement http://www.ebi.ac.uk/efo/EFO_0021254 GCST90243648 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11552 levels 2,170 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11552 measurement http://www.ebi.ac.uk/efo/EFO_0021255 GCST90243649 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11593--O-methylascorbate levels 7,788 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-11593 measurement http://www.ebi.ac.uk/efo/EFO_0020015 GCST90243650 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Adrenate 22:4n6 levels 7,778 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90243651 Genome-wide genotyping array 2023-01-25 36653681 Miyazawa K 2023-01-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36653681 Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction. Atrial fibrillation 77,690 European ancestry cases, 1,167,040 European ancestry controls, 67,864 Japanese ancestry cases, 1,026,594 Japanese ancestry controls NA Illumina [5000630] (imputed) 146 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90204201 Genome-wide genotyping array 2023-01-25 36653681 Miyazawa K 2023-01-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36653681 Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction. Atrial fibrillation 9,826 Japanese ancestry cases, 140,446 Japanese ancestry controls 4,602 Japanese ancestry cases, 44,075 Japanese ancestry controls Illumina [8753038] (imputed) 29 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90244768 Genome-wide genotyping array 2023-01-25 36653681 Miyazawa K 2023-01-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36653681 Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction. Atrial fibrillation 6,825 Japanese ancestry male cases, 74,225 Japanese ancestry male controls NA Illumina [8753038] (imputed) 21 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90244769 Genome-wide genotyping array 2023-01-25 36653681 Miyazawa K 2023-01-19 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36653681 Cross-ancestry genome-wide analysis of atrial fibrillation unveils disease biology and enables cardioembolic risk prediction. Atrial fibrillation 3,001 Japanese ancestry female cases, 66,221 Japanese ancestry female controls NA Illumina [8753038] (imputed) 6 atrial fibrillation http://www.ebi.ac.uk/efo/EFO_0000275 GCST90244770 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phenylalanine-d8 levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phenylalanine-d8 measurement http://www.ebi.ac.uk/efo/EFO_0801214 GCST90257638 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Asymmetric dimethylarginine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 asymmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006522 GCST90257639 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Symmetric dimethylarginine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 symmetrical dimethylarginine measurement http://www.ebi.ac.uk/efo/EFO_0006523 GCST90257640 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-methylarginine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90257641 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Allantoin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90257642 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methylguanidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylguanidine measurement http://www.ebi.ac.uk/efo/EFO_0800011 GCST90257643 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminoisobutyric acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 2-aminoisobutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0801100 GCST90257644 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Kynurenic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 kynurenic acid measurement http://www.ebi.ac.uk/efo/EFO_0010506 GCST90257645 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Carnosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 carnosine measurement http://www.ebi.ac.uk/efo/EFO_0010470 GCST90257646 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-carbamoyl-beta-alanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-carbamoyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0801186 GCST90257647 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thiamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 thiamine measurement http://www.ebi.ac.uk/efo/EFO_0010540 GCST90257648 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90257649 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Niacinamide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 niacinamide measurement http://www.ebi.ac.uk/efo/EFO_0010511 GCST90257650 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Betaine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90257651 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Choline levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90257652 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phosphocholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90257653 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-glycerophosphocholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 alpha-glycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0801110 GCST90257654 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Creatine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90257655 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Creatinine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90257656 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thyroxine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90257657 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Trimethylamine-N-oxide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 plasma trimethylamine N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0005691 GCST90257658 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cytosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257659 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90257660 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 xanthosine measurement http://www.ebi.ac.uk/efo/EFO_0010549 GCST90257661 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pipecolic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0010468 GCST90257662 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801149 GCST90257613 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:6 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801147 GCST90257614 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801144 GCST90257615 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C40:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801152 GCST90257616 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylserine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 C36:3 phosphatidylserine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801139 GCST90257617 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylserine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:2 phosphatidylserine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801137 GCST90257618 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Ceramide (d18:1) levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257619 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:1 Ceramide (d18:1) levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257620 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C14:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801120 GCST90257621 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010392 GCST90257622 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Citrulline levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90257623 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010391 GCST90257624 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010394 GCST90257625 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010393 GCST90257626 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C20:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801126 GCST90257627 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:1 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0010396 GCST90257628 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0010395 GCST90257629 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Diacylglycerol or triacylglycerol fragment levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90257630 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Diacylglycerol or triacylglycerol fragment levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90257631 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Diacylglycerol or triacylglycerol fragment levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90257632 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Taurine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90257633 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-hydroxytryptophan levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90257634 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Serotonin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90257635 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Gamma-aminobutyric acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 GABA measurement http://www.ebi.ac.uk/efo/EFO_0801160 GCST90257636 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Dimethylglycine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90257637 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:1 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257688 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:2 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C14:2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801121 GCST90257689 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257690 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C18 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801122 GCST90257691 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methionine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90257692 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C18:1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801123 GCST90257693 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C18 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801122 GCST90257694 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C26 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257695 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methyladenosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 adenosine measurement http://www.ebi.ac.uk/efo/EFO_0010453 GCST90257696 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylguanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0801093 GCST90257697 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylguanosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0801094 GCST90257698 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylhistamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0801095 GCST90257699 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminooctanoate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90257700 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-deoxyuridine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90257701 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Aspartate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90257702 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-methylguanosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N2-methylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0800634 GCST90257703 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-(N-acetyl-L-cystein-S-yl) acetaminophen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 3-cystein-S-ylacetaminophen measurement http://www.ebi.ac.uk/efo/EFO_0021155 GCST90257704 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methylhistamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0801095 GCST90257705 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methylhistidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90257706 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-acetamidobutanoate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90257707 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-guanidinobutanoic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90257708 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-pyridoxate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90257709 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glutamate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90257710 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Piperine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90257711 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90257712 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0010346 GCST90257713 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90257714 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90257715 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90257716 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:5 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90257717 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90257718 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:3 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90257719 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90257720 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:5 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90257721 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90257722 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Monoacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257723 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Monoacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257724 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:2 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 32.2 measurement http://www.ebi.ac.uk/efo/EFO_0020055 GCST90257725 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:1 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257726 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:0 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0020054 GCST90257727 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0020059 GCST90257728 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90257729 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90257730 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:0 measurement http://www.ebi.ac.uk/efo/EFO_0020058 GCST90257731 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90257732 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90257733 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90257734 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010354 GCST90257735 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:0 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257736 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Diacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90257737 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylnicotinamide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90257663 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Butyrobetaine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 butyrobetaine measurement http://www.ebi.ac.uk/efo/EFO_0801118 GCST90257664 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Putrescine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 putrescine measurement http://www.ebi.ac.uk/efo/EFO_0021810 GCST90257665 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methionine sulfoxide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90257666 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Anserine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90257667 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257668 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C2 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257669 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Serine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90257670 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C3 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257671 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C3-DC-CH3 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C3-DC-CH3 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801128 GCST90257672 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C4 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257673 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C4-OH Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C4-OH carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801150 GCST90257674 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C5 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801153 GCST90257675 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C5:1 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801153 GCST90257676 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C5-DC Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801153 GCST90257677 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C6 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257678 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C7 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C7 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801154 GCST90257679 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C8 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257680 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Threonine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90257681 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C9 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 C9 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801155 GCST90257682 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C10 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257683 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C10:2 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C10:2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0801119 GCST90257684 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C12 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257685 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C12:1 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257686 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14 Carnitine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90257687 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylaspartic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetylaspartic acid measurement http://www.ebi.ac.uk/efo/EFO_0801183 GCST90258138 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Valine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90258139 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylmethionine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90258140 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylornithine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 GCST90258141 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylphenylalanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90258142 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylputrescine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90258143 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylserine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90258144 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetyltryptophan levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800018 GCST90258145 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-alpha-acetylarginine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90258146 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Nicotinuric acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90258147 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-lauroylglycine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-lauroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0801188 GCST90258148 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-methylproline levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90258149 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Leucine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90258150 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Oleoyl glycine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 oleoyl glycine measurement http://www.ebi.ac.uk/efo/EFO_0801207 GCST90258151 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. O-methyladenosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90258152 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pantothenate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90258153 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phenylacetylglutamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90258154 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pro-gly levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 pro-gly measurement http://www.ebi.ac.uk/efo/EFO_0801216 GCST90258155 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pseudouridine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90258156 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pyridoxine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 vitamin B6 measurement http://www.ebi.ac.uk/efo/EFO_0004621 GCST90258157 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Isoleucine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90258158 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Ribothymidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90258159 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sphinganine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90258160 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Trigonelline levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90258161 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Urate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90258162 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthurenate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90258088 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-hydroxy-3-methylbutyrate/hydroxyisovalerate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90258089 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-hydroxytryptophol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 5-hydroxytryptophol measurement http://www.ebi.ac.uk/efo/EFO_0801104 GCST90258090 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-methylcytidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90258091 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-methylcytosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258092 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 6,8-dihydroxypurine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 purine measurement http://www.ebi.ac.uk/efo/EFO_0010526 GCST90258093 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 7-methylguanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90258094 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Acetyl-galactosamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetylgalactosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149 GCST90258095 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Asparagine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90258096 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Allopurinol riboside levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90258097 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-hydroxymetoprolol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258098 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Bilirubin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90258099 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Biliverdin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90258100 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cadaverine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258101 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glutamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90258102 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C-glycosyltryptophan levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90258103 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cortisol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90258104 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cortisone levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90258105 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cystine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90258106 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Diacetylspermine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacetylspermine measurement http://www.ebi.ac.uk/efo/EFO_0801157 GCST90258107 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Dimethylguanido valerate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 carboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0010468 GCST90258108 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Ectoine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ectoine measurement http://www.ebi.ac.uk/efo/EFO_0800953 GCST90258109 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Histidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90258110 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycocholate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90258111 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycodeoxycholate/glycochenodeoxycholate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90258112 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801135 GCST90258213 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:2 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801133 GCST90258214 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801142 GCST90258215 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801138 GCST90258216 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Ornithine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90258217 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801149 GCST90258218 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:6 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801147 GCST90258219 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801144 GCST90258220 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C40:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801152 GCST90258221 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylserine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 C36:3 phosphatidylserine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801139 GCST90258222 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylserine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:2 phosphatidylserine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801137 GCST90258223 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Ceramide (d18:1) levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90258224 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:1 Ceramide (d18:1) levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90258225 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C14:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801120 GCST90258226 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010392 GCST90258227 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Citrulline levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90258228 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010391 GCST90258229 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010394 GCST90258230 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 sphingomyelin 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010393 GCST90258231 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C20:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801126 GCST90258232 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:1 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin 22:1 measurement http://www.ebi.ac.uk/efo/EFO_0010396 GCST90258233 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0010395 GCST90258234 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Diacylglycerol or triacylglycerol fragment levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90258235 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Diacylglycerol or triacylglycerol fragment levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90258236 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Diacylglycerol or triacylglycerol fragment levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90258237 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010369 GCST90258188 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010368 GCST90258189 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010367 GCST90258190 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010370 GCST90258191 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:1 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C20:1 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801127 GCST90258192 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C20:0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801125 GCST90258193 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90258194 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Proline levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90258195 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C30:0 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C30:0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0801129 GCST90258196 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:2 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90258197 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:4 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 34:4 measurement http://www.ebi.ac.uk/efo/EFO_0010378 GCST90258198 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0010377 GCST90258199 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010376 GCST90258200 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010380 GCST90258201 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:3 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801134 GCST90258202 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:5 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801141 GCST90258203 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:7 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801148 GCST90258204 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801132 GCST90258205 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hydroxyproline levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0010498 GCST90258206 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801130 GCST90258207 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801140 GCST90258208 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801136 GCST90258209 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801146 GCST90258210 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801143 GCST90258211 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:6 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C40:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801151 GCST90258212 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Homoarginine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90258115 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Homocitrulline levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90258116 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hypoxanthine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90258117 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Imidazole propionate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90258118 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Arginine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90258119 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indoleacetic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90258120 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90258121 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. L-alpha-glutamyl-L-lysine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90258122 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Linoleoyl ethanolamide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90258123 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Lisinopril levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lisinopril measurement http://www.ebi.ac.uk/efo/EFO_0801175 GCST90258124 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methylimidazoleacetic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylimidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0022082 GCST90258125 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methylthioadenosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90258126 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Myristoleate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90258127 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Lysine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90258128 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N1-acetylspermidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N1-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0801193 GCST90258129 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N1-methyl-2-pyridone-5-carboxamide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90258130 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N2,N2-dimethylguanosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90258131 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N4-acetylcytidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90258132 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6,N6,N6-trimethyllysine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90258133 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6,N6-dimethyllysine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90258134 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6-methyllysine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90258135 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6-acetyllysine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90258136 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylalanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90258137 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Urocanic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 Urocanic acid (RG) measurement http://www.ebi.ac.uk/efo/EFO_0021676 GCST90258163 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Valsartan levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 valsartan measurement http://www.ebi.ac.uk/efo/EFO_0801224 GCST90258164 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Phenylalanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90258165 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90258166 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90258167 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90258168 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90258169 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90258170 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90258171 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90258172 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tyrosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90258173 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:5 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90258174 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:4 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010363 GCST90258175 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:3 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010362 GCST90258176 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:1 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 20:1 measurement http://www.ebi.ac.uk/efo/EFO_0021457 GCST90258177 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010365 GCST90258178 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:5 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021462 GCST90258179 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:4 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021461 GCST90258180 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:0 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0021463 GCST90258181 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Lysophosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258182 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine plasmalogen-A levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258183 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tryptophan levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90258184 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine plasmalogen-B levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258185 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylethanolamine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010366 GCST90258186 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Lysophosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C18:3 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801124 GCST90258187 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Guanidinoacetic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90258113 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Guanine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 guanine measurement http://www.ebi.ac.uk/efo/EFO_0801165 GCST90258114 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-phosphoglycerate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90257403 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-pyridoxate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 4-Pyridoxic acid measurement http://www.ebi.ac.uk/efo/EFO_0021569 GCST90257404 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 6-phosphogluconate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257405 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 7-methylxanthine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90257406 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Acetaminophen glucuronide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 acetaminophen glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801107 GCST90257407 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Aconitate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90257408 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thymine-d4 levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 thymine measurement http://www.ebi.ac.uk/efo/EFO_0800646 GCST90257409 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adonitol/arabitol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ribitol measurement, arabitol measurement http://www.ebi.ac.uk/efo/EFO_0800143, http://www.ebi.ac.uk/efo/EFO_0800148 GCST90257410 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adenosine diphosphate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90257411 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-glycerophosphate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90257412 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-hydroxybutyrate/beta-hydroxybutyrate/hydroxyisobutyrate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257413 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-keto-beta-methylvalerate/alpha-ketoisocaproate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 keto-isocaproic acid KIC / keto-methylvalerate KMV measurement http://www.ebi.ac.uk/efo/EFO_0801173 GCST90257414 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-ketoisovalerate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257415 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adenosine monophosphate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010454 GCST90257416 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Anhydro-D-glucose levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 D-Glucose measurement http://www.ebi.ac.uk/efo/EFO_0021586 GCST90257417 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Aspartate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90257418 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adenosine triphosphate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ATP measurement http://www.ebi.ac.uk/efo/EFO_0801116 GCST90257419 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inosine-15N4 levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90257420 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Chenodeoxycholate/deoxycholate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 deoxycholate measurement, chenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475, http://www.ebi.ac.uk/efo/EFO_0010471 GCST90257421 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Citrate/isocitrate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 isocitrate measurement, citrate measurement http://www.ebi.ac.uk/efo/EFO_0010505, http://www.ebi.ac.uk/efo/EFO_0010114 GCST90257422 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90257423 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cys-gly-oxidized levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90257424 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cystathionine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90257425 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Erythronate/threonate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 erythronate measurement, threonate measurement http://www.ebi.ac.uk/efo/EFO_0021025, http://www.ebi.ac.uk/efo/EFO_0021032 GCST90257426 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Fructose/glucose/galactose levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 fructose measurement, glucose measurement, galactose measurement http://www.ebi.ac.uk/efo/EFO_0010477, http://www.ebi.ac.uk/efo/EFO_0004468, http://www.ebi.ac.uk/efo/EFO_0010481 GCST90257427 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:7 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257353 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90257354 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801132 GCST90257355 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801130 GCST90257356 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 C36:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801140 GCST90257357 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257358 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801136 GCST90257359 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257360 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:0 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257361 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 C38:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801146 GCST90257362 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257363 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801143 GCST90257364 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90257365 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:2 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257366 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:6 Phosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C40:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801151 GCST90257367 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801135 GCST90257368 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:2 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801133 GCST90257369 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801142 GCST90257370 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801140 GCST90257371 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801138 GCST90257372 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801136 GCST90257373 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801149 GCST90257374 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:6 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801147 GCST90257375 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90257376 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801144 GCST90257377 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Fumarate/maleate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 maleate measurement, fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010509, http://www.ebi.ac.uk/efo/EFO_0010480 GCST90257428 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycocholate-d4 levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90257429 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Guanosine diphosphate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 guanosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010494 GCST90257430 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Gentisate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90257431 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glucuronate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90257432 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glutamate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90257433 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycerate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90257434 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycocholate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90257435 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycodeoxycholate/glycochenodeoxycholate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glycochenodeoxycholate measurement, glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490, http://www.ebi.ac.uk/efo/EFO_0010493 GCST90257436 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hippurate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90257437 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Homovanillate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257438 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylhistidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90257439 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hypoxanthine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90257440 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inosine monophosphate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 inosine 5'-monophosphate (IMP) measurement http://www.ebi.ac.uk/efo/EFO_0800641 GCST90257441 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indole-3-propionate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 indole-3-propionate measurement http://www.ebi.ac.uk/efo/EFO_0010501 GCST90257442 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indoleacetate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90257443 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indolelactate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90257444 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inositol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 inositol measurement http://www.ebi.ac.uk/efo/EFO_0010504 GCST90257445 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Isovalerate/valerate/methylbutyrate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 valerate measurement, isovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021112, http://www.ebi.ac.uk/efo/EFO_0021051 GCST90257446 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Kynurenine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90257447 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Lactate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90257448 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Malate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90257449 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylurate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90257450 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Malonate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 malonic acid measurement http://www.ebi.ac.uk/efo/EFO_0801176 GCST90257451 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Malondialdehyde levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257452 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257378 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C40:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801152 GCST90257379 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylserine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90257380 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylserine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90257381 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Ceramide (d18:1) levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257382 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Ceramide (d18:1) levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257383 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:0 Ceramide (d18:1) levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257384 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:1 Ceramide (d18:1) levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257385 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C14:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801120 GCST90257386 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90257387 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257388 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257389 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257390 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257391 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C20:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801126 GCST90257392 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0010395 GCST90257393 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:1 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257394 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:0 Sphingomyelin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingomyelin 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0010397 GCST90257395 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90257396 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90257397 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:5 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90257398 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-hydroxy-3-methylpentanoate/hydroxyisocaproate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257399 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-hydroxyglutarate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90257400 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methyladipate/pimelate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90257401 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methylxanthine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90257402 Genome-wide genotyping array 2023-11-23 37315093 Agren R 2023-06-01 Mol Biol Evol www.ncbi.nlm.nih.gov/pubmed/37315093 Major Genetic Risk Factors for Dupuytren's Disease Are Inherited From Neandertals. Dupuytren's disease 7,871 European ancestry cases, 645,880 European ancestry controls NA NR [12940999] (imputed) 61 Dupuytren Contracture http://www.ebi.ac.uk/efo/EFO_0004229 GCST90297847 Genome-wide genotyping array 2022-12-09 35999636 Wang Y 2022-08-23 Mol Cancer www.ncbi.nlm.nih.gov/pubmed/35999636 A two-stage genome-wide association study to identify novel genetic loci associated with acute radiotherapy toxicity in nasopharyngeal carcinoma. Skin reaction in nasopharyngeal carcinoma treated with radiotherapy 319 Chinese ancestry individuals 765 Chinese ancestry individuals Illumina [4112760] (imputed) 0 response to radiation, skin reaction http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0020927 GCST90165321 Genome-wide genotyping array 2022-12-09 35999636 Wang Y 2022-08-23 Mol Cancer www.ncbi.nlm.nih.gov/pubmed/35999636 A two-stage genome-wide association study to identify novel genetic loci associated with acute radiotherapy toxicity in nasopharyngeal carcinoma. Dysphagia in nasopharyngeal carcinoma treated with radiotherapy 319 Chinese ancestry individuals 765 Chinese ancestry individuals Illumina [4112760] (imputed) 0 response to radiation, Dysphagia http://purl.obolibrary.org/obo/GO_0009314, http://purl.obolibrary.org/obo/HP_0002015 GCST90165322 Genome-wide genotyping array 2022-12-09 35999636 Wang Y 2022-08-23 Mol Cancer www.ncbi.nlm.nih.gov/pubmed/35999636 A two-stage genome-wide association study to identify novel genetic loci associated with acute radiotherapy toxicity in nasopharyngeal carcinoma. Oral mucositis in nasopharyngeal carcinoma treated with radiotherapy 319 Chinese ancestry individuals 765 Chinese ancestry individuals Illumina [4112760] (imputed) 0 oral mucositis, response to radiation http://www.ebi.ac.uk/efo/EFO_1001904, http://purl.obolibrary.org/obo/GO_0009314 GCST90165323 Genome-wide genotyping array 2022-12-09 35999636 Wang Y 2022-08-23 Mol Cancer www.ncbi.nlm.nih.gov/pubmed/35999636 A two-stage genome-wide association study to identify novel genetic loci associated with acute radiotherapy toxicity in nasopharyngeal carcinoma. Salivary gland toxicity in nasopharyngeal carcinoma treated with radiotherapy 319 Chinese ancestry individuals 765 Chinese ancestry individuals Illumina [4112760] (imputed) 0 response to radiation, salivary gland disease http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0008581 GCST90165324 Genome-wide genotyping array 2022-12-09 35999636 Wang Y 2022-08-23 Mol Cancer www.ncbi.nlm.nih.gov/pubmed/35999636 A two-stage genome-wide association study to identify novel genetic loci associated with acute radiotherapy toxicity in nasopharyngeal carcinoma. Myelosuppression in nasopharyngeal carcinoma treated with radiotherapy 319 Chinese ancestry individuals 765 Chinese ancestry individuals Illumina [4112760] (imputed) 0 response to radiation, myelosuppression http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0007053 GCST90165325 Genome-wide genotyping array 2022-12-06 33914752 Weng S 2021-04-29 PLoS One www.ncbi.nlm.nih.gov/pubmed/33914752 Genome-wide association study of antipsychotic-induced sinus bradycardia in Chinese schizophrenia patients. Response to antipsychotic treatment in schizophrenia (sinus bradycardia) 33 Han Chinese ancestry cases, 55 Han Chinese ancestry controls NA Illumina [4632427] (imputed) 0 Bradycardia, response to antipsychotic drug http://purl.obolibrary.org/obo/HP_0001662, http://purl.obolibrary.org/obo/GO_0097332 GCST90239854 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Hypertension complicating pregnancy 10,097 European ancestry cases, 331,138 European ancestry controls NA NR [NR] 5 hypertension, pregnancy-induced http://purl.obolibrary.org/obo/MONDO_0024664 GCST90245819 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Gestational diabetes mellitus 7,395 European ancestry cases, 333,819 European ancestry controls NA NR [NR] 4 gestational diabetes http://www.ebi.ac.uk/efo/EFO_0004593 GCST90245820 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Postnatal depression 14,226 European ancestry cases, 102,414 European ancestry controls NA NR [NR] 0 postpartum depression http://www.ebi.ac.uk/efo/EFO_0007453 GCST90245821 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Ectopic pregnancy 4,021 European ancestry cases, 299,668 European ancestry controls NA NR [NR] 0 Ectopic pregnancy http://purl.obolibrary.org/obo/HP_0031456 GCST90245822 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Spontaneous abortion 12,299 European ancestry cases, 298,762 European ancestry controls NA NR [NR] 0 spontaneous abortion http://www.ebi.ac.uk/efo/EFO_1001255 GCST90245823 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Gestational hypertension without significant proteinuria 5,502 European ancestry cases, 330,237 European ancestry controls NA NR [NR] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90245824 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Hemorrhage in early pregnancy 4,634 European ancestry cases, 323,860 European ancestry controls NA NR [NR] 0 hemorrhage http://purl.obolibrary.org/obo/MP_0001914 GCST90245825 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Excessive vomiting in pregnancy 1,594 European ancestry cases, 324,433 European ancestry controls NA NR [NR] 1 hyperemesis gravidarum http://www.ebi.ac.uk/efo/EFO_1000971 GCST90245826 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Infections of genitourinary tract in pregnancy 1,924 European ancestry cases, 324,489 European ancestry controls NA NR [NR] 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90245827 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Premature rupture of membranes 4,580 European ancestry cases, 316,634 European ancestry controls NA NR [NR] 0 spontaneous preterm birth http://www.ebi.ac.uk/efo/EFO_0006917 GCST90245828 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Placenta praevia 857 European ancestry cases, 317,159 European ancestry controls NA NR [NR] 0 placenta praevia http://www.ebi.ac.uk/efo/EFO_0007442 GCST90245829 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Antepartum hemorrhage 1,879 European ancestry cases, 316,838 European ancestry controls NA NR [NR] 0 Antepartum hemorrhage http://purl.obolibrary.org/obo/HP_0025328 GCST90245830 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. False labour 8,999 European ancestry cases, 316,430 European ancestry controls NA NR [NR] 0 Braxton-Hicks contractions http://www.ebi.ac.uk/efo/EFO_0009639 GCST90245831 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Prolonged pregnancy 2,852 European ancestry cases, 316,832 European ancestry controls NA NR [NR] 0 post term pregnancy http://www.ebi.ac.uk/efo/EFO_0009681 GCST90245832 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Preterm delivery 6,913 European ancestry cases, 310,216 European ancestry controls NA NR [NR] 1 premature birth http://www.ebi.ac.uk/efo/EFO_0003917 GCST90245833 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Abnormalities of forces of labour 2,272 European ancestry cases, 310,213 European ancestry controls NA NR [NR] 0 Abnormal delivery http://purl.obolibrary.org/obo/HP_0001787 GCST90245834 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Long labour 5,786 European ancestry cases, 309,333 European ancestry controls NA NR [NR] 0 post term pregnancy http://www.ebi.ac.uk/efo/EFO_0009681 GCST90245835 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Obstructed labour due to malposition and malpresentation of fetus 4,730 European ancestry cases, 310,159 European ancestry controls NA NR [NR] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90245836 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Labour and delivery complicated by fetal stress 6,468 European ancestry cases, 308,511 European ancestry controls NA NR [NR] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90245837 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Labour and delivery complicated by umbilical cord complications 1,035 European ancestry cases, 310,225 European ancestry controls NA NR [NR] 0 pregnancy disorder http://www.ebi.ac.uk/efo/EFO_0009682 GCST90245838 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Perineal laceration during delivery 5,669 European ancestry cases, 307,316 European ancestry controls NA NR [NR] 0 perineal laceration during delivery http://www.ebi.ac.uk/efo/EFO_0009816 GCST90245839 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Postpartum hemorrhage 5,021 European ancestry cases, 310,086 European ancestry controls NA NR [NR] 0 postpartum hemorrhage http://www.ebi.ac.uk/efo/EFO_0009579 GCST90245840 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Preeclampsia or eclampsia 4,937 European ancestry cases, 330,305 European ancestry controls NA NR [NR] 0 preeclampsia http://www.ebi.ac.uk/efo/EFO_0000668 GCST90245841 Genome-wide genotyping array 2023-02-02 36553520 Changalidis AI 2022-11-30 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36553520 Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications. Supervision of high-risk pregnancy 10,289 European ancestry cases, 300,047 European ancestry controls NA NR [NR] 0 high-risk pregnancy http://www.ebi.ac.uk/efo/EFO_0009573 GCST90245842 Genome-wide genotyping array 2022-12-06 34567510 Song MY 2021-09-14 J Thyroid Res www.ncbi.nlm.nih.gov/pubmed/34567510 Association of Polygenetic Risk Scores Related to Immunity and Inflammation with Hyperthyroidism Risk and Interactions between the Polygenetic Scores and Dietary Factors in a Large Cohort. Hyperthyroidism 842 Korean ancestry cases, 38,799 Korean ancestry controls NA Affymetrix [NR] 4 hyperthyroidism http://www.ebi.ac.uk/efo/EFO_0009189 GCST90054803 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Chiro-inositol levels 2,729 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 inositol measurement http://www.ebi.ac.uk/efo/EFO_0010504 GCST90243877 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 5alpha-androstan-3beta,17beta-diol disulfate levels 7,345 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90243878 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-androsten-3beta,17beta-diol disulfate 1 levels 7,804 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 4-androsten-3beta,17beta-diol disulfate 1 measurement http://www.ebi.ac.uk/efo/EFO_0021113 GCST90243879 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-androsten-3beta,17beta-diol disulfate 2 levels 7,776 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 4-androsten-3beta,17beta-diol disulfate 2 measurement http://www.ebi.ac.uk/efo/EFO_0021114 GCST90243880 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-hydroxyglutarate levels 6,287 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90243881 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Ergothioneine levels 4,453 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90243882 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Palmitoyl sphingomyelin levels 7,814 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90243883 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phenylalanylphenylalanine levels 4,961 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 phenylalanylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021131 GCST90243884 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cis-4-decenoyl carnitine levels 7,660 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90243885 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 15-methylpalmitate isobar with 2-methylpalmitate levels 7,371 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 15-methylpalmitate isobar with 2-methylpalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021052 GCST90243886 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cotinine levels 1,270 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 cotinine measurement http://www.ebi.ac.uk/efo/EFO_0007813 GCST90243887 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 10-undecenoate 11:1n1-to-X-11438 ratio 5,215 European ancestry individuals 1,435 European ancestry individuals Illumina [2100000] (imputed) 2 10-undecenoate 11:1n1-to-X-11438 ratio http://www.ebi.ac.uk/efo/EFO_0021402 GCST90243888 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3- 4-hydroxyphenyl lactate-to-alpha-hydroxyisovalerate ratio 5,442 European ancestry individuals 1,752 European ancestry individuals Illumina [2100000] (imputed) 1 3-4-hydroxyphenyl lactate-to-alpha-hydroxyisovalerate ratio http://www.ebi.ac.uk/efo/EFO_0021513 GCST90243889 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-acetamidobutanoate-to-N1-methyladenosine ratio 4,911 European ancestry individuals 1,606 European ancestry individuals Illumina [2100000] (imputed) 1 4-acetamidobutanoate-to-N1-methyladenosine ratio http://www.ebi.ac.uk/efo/EFO_0021418 GCST90243890 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-acetamidobutanoate-to-X-03056--N-[3-(2-Oxopyrrolidin-1-yl)propyl]acetamide ratio 4,910 European ancestry individuals 1,606 European ancestry individuals Illumina [2100000] (imputed) 1 4-acetamidobutanoate-to-X-03056--N-[3-(2-Oxopyrrolidin-1-yl)propyl]acetamide ratio http://www.ebi.ac.uk/efo/EFO_0021400 GCST90243891 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Acetylcarnitine-to-hexanoylcarnitine ratio 5,568 European ancestry individuals 1,758 European ancestry individuals Illumina [2100000] (imputed) 1 acetylcarnitine-to-hexanoylcarnitine ratio http://www.ebi.ac.uk/efo/EFO_0021514 GCST90243892 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. ADpSGEGDFXAEGGGVR-to-X-14304--leucylalanine ratio 899 European ancestry individuals 1,494 European ancestry individuals Illumina [2100000] (imputed) 1 ADpSGEGDFXAEGGGVR-to-X-14304--leucylalanine ratio http://www.ebi.ac.uk/efo/EFO_0021401 GCST90243893 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. ADSGEGDFXAEGGGVR-to-ADpSGEGDFXAEGGGVR ratio 2,029 European ancestry individuals 1,759 European ancestry individuals Illumina [2100000] (imputed) 3 ADSGEGDFXAEGGGVR-to-ADpSGEGDFXAEGGGVR ratio http://www.ebi.ac.uk/efo/EFO_0021394 GCST90243894 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Androsterone sulfate-to-4-androsten-3beta,17beta-diol disulfate 2 ratio 5,555 European ancestry individuals 1,753 European ancestry individuals Illumina [2100000] (imputed) 2 androsterone sulfate-to-4-androsten-3beta,17beta-diol disulfate 2 ratio http://www.ebi.ac.uk/efo/EFO_0021413 GCST90243895 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Androsterone sulfate-to-epiandrosterone sulfate ratio 5,553 European ancestry individuals 1,759 European ancestry individuals Illumina [2100000] (imputed) 1 androsterone sulfate-to-epiandrosterone sulfate ratio http://www.ebi.ac.uk/efo/EFO_0021515 GCST90243896 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Arachidonate 20:4n6-to-1-arachidonoylglycerophosphoinositol ratio 5,586 European ancestry individuals 1,759 European ancestry individuals Illumina [2100000] (imputed) 1 arachidonate 20:4n6-to-1-arachidonoylglycerophosphoinositol ratio http://www.ebi.ac.uk/efo/EFO_0021397 GCST90243897 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Arachidonate 20:4n6-to-dihomo-linolenate 20:3n3 or n6 ratio 5,589 European ancestry individuals 1,764 European ancestry individuals Illumina [2100000] (imputed) 1 arachidonate 20:4n6-to-dihomo-linolenate 20:3n3 or n6 ratio http://www.ebi.ac.uk/efo/EFO_0021517 GCST90243898 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Aspartylphenylalanine-to-X-14450--phenylalanylleucine ratio 988 European ancestry individuals 1,523 European ancestry individuals Illumina [2100000] (imputed) 1 aspartylphenylalanine-to-X-14450--phenylalanylleucine ratio http://www.ebi.ac.uk/efo/EFO_0021391 GCST90243899 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Betaine-to-pyroglutamine ratio 5,582 European ancestry individuals 1,755 European ancestry individuals Illumina [2100000] (imputed) 1 betaine-to-pyroglutamine ratio http://www.ebi.ac.uk/efo/EFO_0021381 GCST90243900 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. C-glycosyltryptophan-to-succinylcarnitine ratio 5,003 European ancestry individuals 1,527 European ancestry individuals Illumina [2100000] (imputed) 1 C-glycosyltryptophan-to-succinylcarnitine ratio http://www.ebi.ac.uk/efo/EFO_0021416 GCST90243901 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Carnitine-to-X-12798 ratio 5,454 European ancestry individuals 1,644 European ancestry individuals Illumina [2100000] (imputed) 1 carnitine-to-X-12798 ratio http://www.ebi.ac.uk/efo/EFO_0021403 GCST90243902 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. DHEA-S-to-4-androsten-3beta,17beta-diol disulfate 2 ratio 5,571 European ancestry individuals 1,757 European ancestry individuals Illumina [2100000] (imputed) 1 DHEA-S-to-4-androsten-3beta,17beta-diol disulfate 2 ratio http://www.ebi.ac.uk/efo/EFO_0021411 GCST90243903 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Docosapentaenoate n3 DPA; 22:5n3-to-X-12627 ratio 5,428 European ancestry individuals 1,559 European ancestry individuals Illumina [2100000] (imputed) 1 docosapentaenoate n3 DPA; 22:5n3-to-X-12627 ratio http://www.ebi.ac.uk/efo/EFO_0021389 GCST90243904 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. DSGEGDFXAEGGGVR-to-ADpSGEGDFXAEGGGVR ratio 2,019 European ancestry individuals 1,758 European ancestry individuals Illumina [2100000] (imputed) 3 DSGEGDFXAEGGGVR-to-ADpSGEGDFXAEGGGVR ratio http://www.ebi.ac.uk/efo/EFO_0021395 GCST90243905 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glucose-to-mannose ratio 5,568 European ancestry individuals 1,744 European ancestry individuals Illumina [2100000] (imputed) 1 glucose-to-mannose ratio http://www.ebi.ac.uk/efo/EFO_0021404 GCST90243906 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glutamine-to-histidine ratio 5,591 European ancestry individuals 1,762 European ancestry individuals Illumina [2100000] (imputed) 1 glutamine-to-histidine ratio http://www.ebi.ac.uk/efo/EFO_0021420 GCST90243907 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hexanoylcarnitine-to-octanoylcarnitine ratio 5,568 European ancestry individuals 1,763 European ancestry individuals Illumina [2100000] (imputed) 1 hexanoylcarnitine-to-octanoylcarnitine ratio http://www.ebi.ac.uk/efo/EFO_0021410 GCST90243908 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Indoleacetate-to-N2,N2-dimethylguanosine ratio 4,016 European ancestry individuals 812 European ancestry individuals Illumina [2100000] (imputed) 1 indoleacetate-to-N2,N2-dimethylguanosine ratio http://www.ebi.ac.uk/efo/EFO_0021396 GCST90243909 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Isoleucine-to-X-11529 ratio 5,086 European ancestry individuals 1,143 European ancestry individuals Illumina [2100000] (imputed) 1 isoleucine-to-X-11529 ratio http://www.ebi.ac.uk/efo/EFO_0021406 GCST90243910 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Linoleate 18:2n6-to-dihomo-linolenate 20:3n3 or n6 ratio 5,559 European ancestry individuals 1,762 European ancestry individuals Illumina [2100000] (imputed) 1 linoleate 18:2n6-to-dihomo-linolenate 20:3n3 or n6 ratio http://www.ebi.ac.uk/efo/EFO_0021518 GCST90243911 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Linoleate 18:2n6-to-X-12442--5,8-tetradecadienoate ratio 5,540 European ancestry individuals 1,762 European ancestry individuals Illumina [2100000] (imputed) 1 linoleate 18:2n6-to-X-12442-5,8-tetradecadienoate ratio http://www.ebi.ac.uk/efo/EFO_0021519 GCST90243912 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Lysine-to-glutaroyl carnitine ratio 5,532 European ancestry individuals 1,714 European ancestry individuals Illumina [2100000] (imputed) 2 lysine-to-glutaroyl carnitine ratio http://www.ebi.ac.uk/efo/EFO_0021390 GCST90243913 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Myristate 14:0-to-myristoleate 14:1n5 ratio 5,585 European ancestry individuals 1,767 European ancestry individuals Illumina [2100000] (imputed) 1 myristate 14:0-to-myristoleate 14:1n5 ratio http://www.ebi.ac.uk/efo/EFO_0021419 GCST90243914 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N-acetylornithine-to-myo-inositol ratio 5,385 European ancestry individuals 1,742 European ancestry individuals Illumina [2100000] (imputed) 1 N-acetylornithine-to-myo-inositol ratio http://www.ebi.ac.uk/efo/EFO_0021382 GCST90243915 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Octanoylcarnitine-to-X-13435 ratio 5,000 European ancestry individuals 1,522 European ancestry individuals Illumina [2100000] (imputed) 1 octanoylcarnitine-to-X-13435 ratio http://www.ebi.ac.uk/efo/EFO_0021386 GCST90243916 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phenyllactate-to-phenylalanine ratio 4,622 European ancestry individuals 1,070 European ancestry individuals Illumina [2100000] (imputed) 1 phenyllactate-to-phenylalanine ratio http://www.ebi.ac.uk/efo/EFO_0021521 GCST90243917 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phosphate-to-erythronate ratio 5,546 European ancestry individuals 1,732 European ancestry individuals Illumina [2100000] (imputed) 1 phosphate-to-erythronate ratio http://www.ebi.ac.uk/efo/EFO_0021384 GCST90243918 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Propionylcarnitine-to-isovalerylcarnitine ratio 5,584 European ancestry individuals 1,753 European ancestry individuals Illumina [2100000] (imputed) 1 propionylcarnitine-to-isovalerylcarnitine ratio http://www.ebi.ac.uk/efo/EFO_0021385 GCST90243919 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Urate-to-histidine ratio 5,591 European ancestry individuals 1,761 European ancestry individuals Illumina [2100000] (imputed) 1 urate-to-histidine ratio http://www.ebi.ac.uk/efo/EFO_0021409 GCST90243920 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Valine-to-isovalerylcarnitine ratio 5,580 European ancestry individuals 1,750 European ancestry individuals Illumina [2100000] (imputed) 1 valine-to-isovalerylcarnitine ratio http://www.ebi.ac.uk/efo/EFO_0021387 GCST90243921 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Valine-to-proline ratio 5,591 European ancestry individuals 1,762 European ancestry individuals Illumina [2100000] (imputed) 1 valine-to-proline ratio http://www.ebi.ac.uk/efo/EFO_0021414 GCST90243922 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-04499--3,4-dihydroxybutyrate-to-C-glycosyltryptophan ratio 4,942 European ancestry individuals 1,577 European ancestry individuals Illumina [2100000] (imputed) 1 X-04499--3,4-dihydroxybutyrate-to-C-glycosyltryptophan ratio http://www.ebi.ac.uk/efo/EFO_0021415 GCST90243923 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-08402-to-cholesterol ratio 5,525 European ancestry individuals 1,752 European ancestry individuals Illumina [2100000] (imputed) 1 X-08402-to-cholesterol ratio http://www.ebi.ac.uk/efo/EFO_0021383 GCST90243924 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-10510-to-palmitoyl sphingomyelin ratio 5,586 European ancestry individuals 1,757 European ancestry individuals Illumina [2100000] (imputed) 1 X-10510-to-palmitoyl sphingomyelin ratio http://www.ebi.ac.uk/efo/EFO_0021398 GCST90243925 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11315-to-pyroglutamine ratio 5,560 European ancestry individuals 1,758 European ancestry individuals Illumina [2100000] (imputed) 1 X-11315-to-pyroglutamine ratio http://www.ebi.ac.uk/efo/EFO_0021407 GCST90243926 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12441--12-hydroxyeicosatetraenoate 12-HETE levels 2,761 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12441--12-hydroxyeicosatetraenoate 12-HETE measurement http://www.ebi.ac.uk/efo/EFO_0021307 GCST90243727 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12442--5,8-tetradecadienoate levels 7,780 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X12442--5,8-tetradecadienoate measurement http://www.ebi.ac.uk/efo/EFO_0021308 GCST90243728 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12443 levels 5,357 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12443 measurement http://www.ebi.ac.uk/efo/EFO_0021309 GCST90243729 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12450 levels 6,432 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12450 measurement http://www.ebi.ac.uk/efo/EFO_0021310 GCST90243730 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12456 levels 4,774 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-12456 measurement http://www.ebi.ac.uk/efo/EFO_0021311 GCST90243731 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12465 levels 5,883 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12465 measurement http://www.ebi.ac.uk/efo/EFO_0021312 GCST90243732 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Piperine levels 7,173 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90243733 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Octanoylcarnitine levels 7,790 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90243734 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Alpha-hydroxyisovalerate levels 7,668 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 3-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0010984 GCST90243735 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N-acetylthreonine levels 6,909 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90243736 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Decanoylcarnitine levels 7,766 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90243737 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-palmitoylglycerophosphocholine levels 7,803 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-palmitoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021089 GCST90243738 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-heptadecanoylglycerophosphocholine levels 7,422 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-heptadecanoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021082 GCST90243739 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-oleoylglycerophosphocholine levels 7,812 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-oleoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021086 GCST90243740 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-stearoylglycerophosphocholine levels 7,817 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-stearoylglycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0021092 GCST90243741 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 5-dodecenoate 12:1n7 levels 7,770 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 5-dodecenoate 12:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021100 GCST90243742 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Stearidonate 18:4n3 levels 7,775 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90243743 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 10-heptadecenoate 17:1n7 levels 7,795 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 10-heptadecenoate 17:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021060 GCST90243744 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 10-nonadecenoate 19:1n9 levels 7,789 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90243745 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Epiandrosterone sulfate levels 7,769 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90243746 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Linolenate [alpha or gamma; 18:3n3 or 6] levels 7,786 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90243747 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12510--2-aminooctanoic acid levels 7,566 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-12510--2-aminooctanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0021313 GCST90243748 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12524 levels 7,809 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-12524 measurement http://www.ebi.ac.uk/efo/EFO_0021314 GCST90243749 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Bilirubin (E,Z or Z,E) levels 5,295 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90243750 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Metoprolol acid metabolite levels 286 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 metoprolol acid metabolite measurement http://www.ebi.ac.uk/efo/EFO_0021159 GCST90243751 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11440-to-4-androsten-3beta,17beta-diol disulfate 2 ratio 5,485 European ancestry individuals 1,756 European ancestry individuals Illumina [2100000] (imputed) 1 X-11440-to-4-androsten-3beta,17beta-diol disulfate 2 ratio http://www.ebi.ac.uk/efo/EFO_0021393 GCST90243927 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11444-to-X-11470 ratio 5,259 European ancestry individuals 1,586 European ancestry individuals Illumina [2100000] (imputed) 1 X-11444-to-X-11470 ratio http://www.ebi.ac.uk/efo/EFO_0021412 GCST90243928 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11444-to-X-12844 ratio 5,570 European ancestry individuals 1,731 European ancestry individuals Illumina [2100000] (imputed) 1 X-11444-to-X-12844 ratio http://www.ebi.ac.uk/efo/EFO_0021405 GCST90243929 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11820-to-cholesterol ratio 5,509 European ancestry individuals 1,747 European ancestry individuals Illumina [2100000] (imputed) 1 X-11820-to-cholesterol ratio http://www.ebi.ac.uk/efo/EFO_0021392 GCST90243930 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12038-to-bradykinin, des-arg 9 ratio 2,932 European ancestry individuals 1,480 European ancestry individuals Illumina [2100000] (imputed) 1 X-12038-to-bradykinin, des-arg 9 ratio http://www.ebi.ac.uk/efo/EFO_0021388 GCST90243931 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12095--N1-methyl-3-pyridone-4-carboxamide-to-X-12844 ratio 5,526 European ancestry individuals 1,692 European ancestry individuals Illumina [2100000] (imputed) 1 X-12095--N1-methyl-3-pyridone-4-carboxamide-to-X-12844 ratio http://www.ebi.ac.uk/efo/EFO_0021399 GCST90243932 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-12798-to-phenylalanine ratio 5,458 European ancestry individuals 1,645 European ancestry individuals Illumina [2100000] (imputed) 1 X-12798-to-phenylalanine ratio http://www.ebi.ac.uk/efo/EFO_0021417 GCST90243933 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-13215-to-X-13671 ratio 4,651 European ancestry individuals 1,027 European ancestry individuals Illumina [2100000] (imputed) 1 X-13215-to-X-13671 ratio http://www.ebi.ac.uk/efo/EFO_0021408 GCST002442 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Imidazole propionate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90257513 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Arginine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90257514 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indoleacetic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90257515 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90257516 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. L-alpha-glutamyl-L-lysine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90257517 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Linoleoyl ethanolamide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90257518 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Lisinopril levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lisinopril measurement http://www.ebi.ac.uk/efo/EFO_0801175 GCST90257519 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methylimidazoleacetic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 1-methylimidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0022082 GCST90257520 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Methylthioadenosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90257521 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Myristoleate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90257522 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Lysine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90257523 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N1-acetylspermidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N1-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0801193 GCST90257524 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N1-methyl-2-pyridone-5-carboxamide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90257525 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N2,N2-dimethylguanosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90257526 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N4-acetylcytidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90257527 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6,N6,N6-trimethyllysine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90257528 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6,N6-dimethyllysine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90257529 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6-methyllysine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90257530 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N6-acetyllysine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90257531 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylalanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90257532 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylaspartic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetylaspartic acid measurement http://www.ebi.ac.uk/efo/EFO_0801183 GCST90257533 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Valine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90257534 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylmethionine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90257535 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylornithine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 GCST90257536 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylphenylalanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90257537 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:6 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90257913 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:4 measurement http://www.ebi.ac.uk/efo/EFO_0010431 GCST90257914 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:3 measurement http://www.ebi.ac.uk/efo/EFO_0010430 GCST90257915 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:2 measurement http://www.ebi.ac.uk/efo/EFO_0010429 GCST90257916 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:11 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:11 measurement http://www.ebi.ac.uk/efo/EFO_0010438 GCST90257917 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:10 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257918 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010375 GCST90257919 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:9 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:9 measurement http://www.ebi.ac.uk/efo/EFO_0010443 GCST90257920 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:8 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90257921 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:7 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:7 measurement http://www.ebi.ac.uk/efo/EFO_0010441 GCST90257922 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:6 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 58:6 measurement http://www.ebi.ac.uk/efo/EFO_0010440 GCST90257923 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C60:12 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 60:12 measurement http://www.ebi.ac.uk/efo/EFO_0010444 GCST90257924 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257925 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90257926 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylcholine-A levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 phosphatidylcholine 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0010382 GCST90257927 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylcholine-B levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0010382 GCST90257928 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0010381 GCST90257929 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010380 GCST90257930 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010379 GCST90257931 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:0 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 36:0 measurement http://www.ebi.ac.uk/efo/EFO_0021473 GCST90257932 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 38:6 measurement http://www.ebi.ac.uk/efo/EFO_0010388 GCST90257933 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 phosphatidylcholine 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0010386 GCST90257934 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:3 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 38:3 measurement http://www.ebi.ac.uk/efo/EFO_0010385 GCST90257935 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:2 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 phosphatidylcholine 38:2 measurement http://www.ebi.ac.uk/efo/EFO_0010384 GCST90257936 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90257937 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:0 measurement http://www.ebi.ac.uk/efo/EFO_0021480 GCST90257888 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C51:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257889 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C51:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90257890 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:7 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257891 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C51:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 51:0 measurement http://www.ebi.ac.uk/efo/EFO_0021481 GCST90257892 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90257893 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90257894 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90257895 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 52:1 measurement http://www.ebi.ac.uk/efo/EFO_0010413 GCST90257896 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0010377 GCST90257897 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257898 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C53:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257899 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:9 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:9 measurement http://www.ebi.ac.uk/efo/EFO_0010427 GCST90257900 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C53:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90257901 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:8 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:8 measurement http://www.ebi.ac.uk/efo/EFO_0010426 GCST90257902 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90257903 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90257904 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90257905 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:2 measurement http://www.ebi.ac.uk/efo/EFO_0010420 GCST90257906 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 54:1 measurement http://www.ebi.ac.uk/efo/EFO_0010419 GCST90257907 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010376 GCST90257908 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:10 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:10 measurement http://www.ebi.ac.uk/efo/EFO_0010428 GCST90257909 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C55:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257910 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C55:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257911 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:8 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90257912 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:9 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257938 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:6 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 40:6 measurement http://www.ebi.ac.uk/efo/EFO_0010389 GCST90257939 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 hydroxy-Phosphatidylcholine-A levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257940 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 hydroxy-Phosphatidylcholine-B levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257941 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 hydroxy-Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257942 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:5 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257943 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:3 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801134 GCST90257944 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257945 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Phosphatidylcholine plasmalogen-A levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257946 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Phosphatidylcholine plasmalogen-B levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257947 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90257948 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylcholine plasmalogen-A levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:5 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801141 GCST90257949 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylcholine plasmalogen-B levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:5 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801141 GCST90257950 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257951 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257952 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257953 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257954 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:7 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801148 GCST90257955 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:6 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801145 GCST90257956 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257957 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:7 Phosphatidylcholine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257958 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:3 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 18:3 measurement http://www.ebi.ac.uk/efo/EFO_0021454 GCST90257959 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801132 GCST90257960 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801130 GCST90257961 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 1 C36:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801140 GCST90257962 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257863 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:1 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 32:1 measurement http://www.ebi.ac.uk/efo/EFO_0010373 GCST90257864 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 NH4_C46:3 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801205 GCST90257865 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 NH4_C46:2 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801204 GCST90257866 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 46:0 measurement http://www.ebi.ac.uk/efo/EFO_0010400 GCST90257867 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 46:0 measurement http://www.ebi.ac.uk/efo/EFO_0010400 GCST90257868 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C47:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257869 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C47:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257870 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C47:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257871 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257872 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:4 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:4 measurement http://www.ebi.ac.uk/efo/EFO_0010407 GCST90257873 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90257874 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:0 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0010372 GCST90257875 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90257876 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90257877 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257878 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257879 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90257880 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:0 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257881 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left posterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104908 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left sub-parietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104909 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left central sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104910 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left calloso-marginal anterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104911 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left superior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104912 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left calloso-marginal posterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104913 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left anterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104914 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left superior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104915 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left posterior lateral fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104916 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left intraparietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104917 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the left inferior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104918 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right posterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104919 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right sub-parietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104920 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right central sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104921 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right calloso-marginal anterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104922 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right superior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104923 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right calloso-marginal posterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104924 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right anterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104925 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right superior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104926 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right posterior lateral fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104927 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right intraparietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104928 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal depth of the right inferior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal depth http://www.ebi.ac.uk/efo/EFO_0022047 GCST90104929 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left posterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104930 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left sub-parietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104931 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left central sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104932 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left calloso-marginal anterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104933 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left superior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104934 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left calloso-marginal posterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104935 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left anterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104936 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left superior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104937 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left posterior lateral fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104938 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left intraparietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104939 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the left inferior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104940 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right posterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104941 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right sub-parietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104942 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right central sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104943 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right calloso-marginal anterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104944 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right superior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104945 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right calloso-marginal posterior fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 3 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104946 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right anterior inferior temporal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104947 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right superior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104948 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right posterior lateral fissure 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104949 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right intraparietal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104950 Genome-wide genotyping array 2023-01-09 36442731 Lemaitre H 2022-11-25 Neuroimage www.ncbi.nlm.nih.gov/pubmed/36442731 Genetic variations within human gained enhancer elements affect human brain sulcal morphology. Sulcal opening distance of the right inferior frontal sulcus 18,101 Bristish ancestry individuals NA Affymetrix [8954808] (imputed) 0 sulcal opening distance http://www.ebi.ac.uk/efo/EFO_0022046 GCST90104951 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:6 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257882 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:5 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:5 measurement http://www.ebi.ac.uk/efo/EFO_0010412 GCST90257883 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:3 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90257884 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:2 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90257885 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:4 Phosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylcholine 34:4 measurement http://www.ebi.ac.uk/efo/EFO_0010378 GCST90257886 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:1 Triacylglycerol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90257887 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Aconitate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90258013 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thymine-d4 levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 thymine measurement http://www.ebi.ac.uk/efo/EFO_0800646 GCST90258014 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adonitol/arabitol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ribitol measurement, arabitol measurement http://www.ebi.ac.uk/efo/EFO_0800143, http://www.ebi.ac.uk/efo/EFO_0800148 GCST90258015 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adenosine diphosphate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90258016 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-glycerophosphate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90258017 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-hydroxybutyrate/beta-hydroxybutyrate/hydroxyisobutyrate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258018 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-keto-beta-methylvalerate/alpha-ketoisocaproate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 keto-isocaproic acid KIC / keto-methylvalerate KMV measurement http://www.ebi.ac.uk/efo/EFO_0801173 GCST90258019 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-ketoisovalerate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90258020 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adenosine monophosphate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010454 GCST90258021 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Anhydro-D-glucose levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 D-Glucose measurement http://www.ebi.ac.uk/efo/EFO_0021586 GCST90258022 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Aspartate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90258023 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Adenosine triphosphate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ATP measurement http://www.ebi.ac.uk/efo/EFO_0801116 GCST90258024 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inosine-15N4 levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90258025 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Chenodeoxycholate/deoxycholate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 deoxycholate measurement, chenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475, http://www.ebi.ac.uk/efo/EFO_0010471 GCST90258026 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Citrate/isocitrate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 isocitrate measurement, citrate measurement http://www.ebi.ac.uk/efo/EFO_0010505, http://www.ebi.ac.uk/efo/EFO_0010114 GCST90258027 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90258028 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cys-gly-oxidized levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90258029 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cystathionine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90258030 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Erythronate/threonate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 erythronate measurement, threonate measurement http://www.ebi.ac.uk/efo/EFO_0021025, http://www.ebi.ac.uk/efo/EFO_0021032 GCST90258031 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Fructose/glucose/galactose levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 fructose measurement, glucose measurement, galactose measurement http://www.ebi.ac.uk/efo/EFO_0010477, http://www.ebi.ac.uk/efo/EFO_0004468, http://www.ebi.ac.uk/efo/EFO_0010481 GCST90258032 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Fumarate/maleate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 maleate measurement, fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010509, http://www.ebi.ac.uk/efo/EFO_0010480 GCST90258033 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycocholate-d4 levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90258034 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Guanosine diphosphate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 guanosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010494 GCST90258035 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Gentisate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90258036 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glucuronate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90258037 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glutamate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90258038 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycerate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90258039 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycocholate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90258040 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycodeoxycholate/glycochenodeoxycholate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 glycochenodeoxycholate measurement, glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490, http://www.ebi.ac.uk/efo/EFO_0010493 GCST90258041 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hippurate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90258042 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Homovanillate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258043 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylhistidine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90258044 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hypoxanthine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90258045 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inosine monophosphate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 inosine 5'-monophosphate (IMP) measurement http://www.ebi.ac.uk/efo/EFO_0800641 GCST90258046 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indole-3-propionate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 indole-3-propionate measurement http://www.ebi.ac.uk/efo/EFO_0010501 GCST90258047 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indoleacetate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90258048 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Indolelactate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90258049 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Inositol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 inositol measurement http://www.ebi.ac.uk/efo/EFO_0010504 GCST90258050 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Isovalerate/valerate/methylbutyrate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 valerate measurement, isovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021112, http://www.ebi.ac.uk/efo/EFO_0021051 GCST90258051 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Kynurenine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90258052 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Lactate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90258053 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Malate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90258054 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 1-methylurate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 1-methylurate measurement http://www.ebi.ac.uk/efo/EFO_0021173 GCST90258055 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Malonate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 malonic acid measurement http://www.ebi.ac.uk/efo/EFO_0801176 GCST90258056 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Malondialdehyde levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258057 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Mesaconate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90258058 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylcarnosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022101 GCST90258059 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylglutamate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90258060 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Oxalate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90258061 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pantothenate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90258062 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Propionate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 propionic acid measurement http://www.ebi.ac.uk/efo/EFO_0010525 GCST90258063 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pseudouridine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90258064 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminoadipate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0800137 GCST90258065 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Quinate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90258066 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Quinolinate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90258067 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Salicylurate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90258068 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sebacate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90258069 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sorbitol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0010533 GCST90258070 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Suberate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90258071 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Succinate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90258072 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Succinyladenosine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 adenosine measurement http://www.ebi.ac.uk/efo/EFO_0010453 GCST90258073 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sucrose/lactose/trehalose levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sucrose measurement, lactose measurement, D-Trehalose measurement http://www.ebi.ac.uk/efo/EFO_0010535, http://www.ebi.ac.uk/efo/EFO_0010507, http://www.ebi.ac.uk/efo/EFO_0021592 GCST90258074 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminobutyrate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90258075 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tartarate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90258076 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Taurocholate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90258077 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Taurodeoxycholate/taurochenodeoxycholate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90258078 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Threitol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 threitol measurement http://www.ebi.ac.uk/efo/EFO_0021031 GCST90258079 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thymine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 thymine measurement http://www.ebi.ac.uk/efo/EFO_0800646 GCST90258080 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tocopherol levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0004738 GCST90258081 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Uridine diphosphate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 uridine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010545 GCST90258082 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Uracil levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 uracil measurement http://www.ebi.ac.uk/efo/EFO_0800644 GCST90258083 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Urate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90258084 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminoheptanoate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90258085 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Uridine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90258086 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90258087 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Ceramide (d18:1) levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257988 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:0 Ceramide (d18:1) levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257989 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:1 Ceramide (d18:1) levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257990 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C14:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801120 GCST90257991 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010359 GCST90257992 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257993 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257994 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257995 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257996 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C20:0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0801126 GCST90257997 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin 22:0 measurement http://www.ebi.ac.uk/efo/EFO_0010395 GCST90257998 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:1 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90257999 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C24:0 Sphingomyelin levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 sphingomyelin 24:0 measurement http://www.ebi.ac.uk/efo/EFO_0010397 GCST90258000 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester measurement http://www.ebi.ac.uk/efo/EFO_0010351 GCST90258001 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Cholesteryl ester levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90258002 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C20:5 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010364 GCST90258003 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-hydroxy-3-methylpentanoate/hydroxyisocaproate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90258004 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-hydroxyglutarate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90258005 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methyladipate/pimelate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90258006 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-methylxanthine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90258007 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 3-phosphoglycerate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90258008 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 4-pyridoxate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 4-Pyridoxic acid measurement http://www.ebi.ac.uk/efo/EFO_0021569 GCST90258009 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 6-phosphogluconate levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90258010 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 7-methylxanthine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90258011 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Acetaminophen glucuronide levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 acetaminophen glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801107 GCST90258012 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257963 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801136 GCST90257964 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257965 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:0 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257966 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801146 GCST90257967 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257968 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801143 GCST90257969 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:2 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010361 GCST90257970 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:2 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257971 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:6 Phosphatidylethanolamine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C40:6 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801151 GCST90257972 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801135 GCST90257973 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C34:2 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801133 GCST90257974 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801142 GCST90257975 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:4 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801140 GCST90257976 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:3 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801138 GCST90257977 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C36:2 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0801136 GCST90257978 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801149 GCST90257979 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:6 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801147 GCST90257980 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C18:1 Lysophosphatidylcholine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 lysophosphatidylcholine 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010360 GCST90257981 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:5 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C38:5 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801144 GCST90257982 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:3 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010228 GCST90257983 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:7 Phosphatidylethanolamine plasmalogen levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 C40:7 phosphatidylethanolamine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801152 GCST90257984 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylserine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90257985 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylserine levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 phosphatidylserines measurement http://www.ebi.ac.uk/efo/EFO_0020049 GCST90257986 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Ceramide (d18:1) levels in chronic kidney disease 687 African American individuals NA Illumina [15449934] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90257987 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Dimethylguanido valerate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 carboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0010468 GCST90257503 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Ectoine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ectoine measurement http://www.ebi.ac.uk/efo/EFO_0800953 GCST90257504 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Histidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90257505 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycocholate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90257506 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glycodeoxycholate/glycochenodeoxycholate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90257507 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Guanidinoacetic acid levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90257508 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Guanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 guanine measurement http://www.ebi.ac.uk/efo/EFO_0801165 GCST90257509 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Homoarginine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 amino acid measurement http://www.ebi.ac.uk/efo/EFO_0005134 GCST90257510 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Homocitrulline levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90257511 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Hypoxanthine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90257512 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Uracil levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 uracil measurement http://www.ebi.ac.uk/efo/EFO_0800644 GCST90257478 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Urate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90257479 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminoheptanoate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90257480 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Uridine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90257481 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90257482 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Xanthurenate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90257483 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-hydroxy-3-methylbutyrate/hydroxyisovalerate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90257484 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-hydroxytryptophol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 5-hydroxytryptophol measurement http://www.ebi.ac.uk/efo/EFO_0801104 GCST90257485 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-methylcytidine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90257486 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 5-methylcytosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257487 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 6,8-dihydroxypurine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 purine measurement http://www.ebi.ac.uk/efo/EFO_0010526 GCST90257488 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 7-methylguanine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90257489 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Acetyl-galactosamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetylgalactosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149 GCST90257490 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Asparagine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90257491 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Allopurinol riboside levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 nucleoside measurement http://www.ebi.ac.uk/efo/EFO_0010512 GCST90257492 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Alpha-hydroxymetoprolol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257493 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Bilirubin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90257494 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Biliverdin levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90257495 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cadaverine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90257496 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Glutamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90257497 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C-glycosyltryptophan levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90257498 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cortisol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90257499 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cortisone levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90257500 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cystine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90257501 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Diacetylspermine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacetylspermine measurement http://www.ebi.ac.uk/efo/EFO_0801157 GCST90257502 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Mesaconate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 fumarate measurement http://www.ebi.ac.uk/efo/EFO_0010480 GCST90257453 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylcarnosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022101 GCST90257454 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. N-acetylglutamate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90257455 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Oxalate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90257456 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pantothenate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90257457 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Propionate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 propionic acid measurement http://www.ebi.ac.uk/efo/EFO_0010525 GCST90257458 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Pseudouridine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90257459 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminoadipate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0800137 GCST90257460 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Quinate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90257461 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Quinolinate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90257462 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Salicylurate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90257463 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sebacate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90257464 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sorbitol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0010533 GCST90257465 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Suberate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90257466 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Succinate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90257467 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Succinyladenosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 adenosine measurement http://www.ebi.ac.uk/efo/EFO_0010453 GCST90257468 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sucrose/lactose/trehalose levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sucrose measurement, lactose measurement, D-Trehalose measurement http://www.ebi.ac.uk/efo/EFO_0010535, http://www.ebi.ac.uk/efo/EFO_0010507, http://www.ebi.ac.uk/efo/EFO_0021592 GCST90257469 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. 2-aminobutyrate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90257470 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tartarate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90257471 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Taurocholate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90257472 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Taurodeoxycholate/taurochenodeoxycholate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90257473 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Threitol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 threitol measurement http://www.ebi.ac.uk/efo/EFO_0021031 GCST90257474 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Thymine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 thymine measurement http://www.ebi.ac.uk/efo/EFO_0800646 GCST90257475 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Tocopherol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0004738 GCST90257476 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Uridine diphosphate levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 uridine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010545 GCST90257477 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C56:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:2 measurement http://www.ebi.ac.uk/efo/EFO_0010429 GCST90257203 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C58:11 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:11 measurement http://www.ebi.ac.uk/efo/EFO_0010438 GCST90257204 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:6 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010371 GCST90257205 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C58:10 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:10 measurement http://www.ebi.ac.uk/efo/EFO_0010437 GCST90257206 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C58:9 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:9 measurement http://www.ebi.ac.uk/efo/EFO_0010443 GCST90257207 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C60:12 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 60:12 measurement http://www.ebi.ac.uk/efo/EFO_0010444 GCST90257208 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Campesterol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90257209 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Cholesterol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90257210 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Coenzyme Q9 levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 ubiquinone measurement http://www.ebi.ac.uk/efo/EFO_0021486 GCST90257211 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Palmitoylethanolamide levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257212 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. Sphingosine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90257213 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C14:0 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010340 GCST90257214 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C22:0 Lysophosphatidylethanolamine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0010225 GCST90257215 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C16:1 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010342 GCST90257216 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C16:0 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010341 GCST90257217 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:2 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 18:2 measurement http://www.ebi.ac.uk/efo/EFO_0010345 GCST90257218 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:1 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 18:1 measurement http://www.ebi.ac.uk/efo/EFO_0010344 GCST90257219 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:0 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0010343 GCST90257220 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C20:5 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 20:5 measurement http://www.ebi.ac.uk/efo/EFO_0010349 GCST90257221 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C20:4 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 20:4 measurement http://www.ebi.ac.uk/efo/EFO_0010348 GCST90257222 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C20:3 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 20:3 measurement http://www.ebi.ac.uk/efo/EFO_0010347 GCST90257223 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C22:6 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 22:6 measurement http://www.ebi.ac.uk/efo/EFO_0010350 GCST90257224 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C22:5 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 cholesteryl ester 22:5 measurement http://www.ebi.ac.uk/efo/EFO_0021444 GCST90257225 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C30:1 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257226 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C22:4 Cholesteryl ester levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 cholesteryl ester 22:4 measurement http://www.ebi.ac.uk/efo/EFO_0021443 GCST90257227 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010376 GCST90257303 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:10 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:10 measurement http://www.ebi.ac.uk/efo/EFO_0010428 GCST90257304 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C55:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257305 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C55:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257306 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:8 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:8 measurement http://www.ebi.ac.uk/efo/EFO_0010435 GCST90257307 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:6 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:6 measurement http://www.ebi.ac.uk/efo/EFO_0010433 GCST90257308 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:4 measurement http://www.ebi.ac.uk/efo/EFO_0010431 GCST90257309 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:3 measurement http://www.ebi.ac.uk/efo/EFO_0010430 GCST90257310 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C56:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 56:2 measurement http://www.ebi.ac.uk/efo/EFO_0010429 GCST90257311 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:11 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:11 measurement http://www.ebi.ac.uk/efo/EFO_0010438 GCST90257312 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:10 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257313 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010375 GCST90257314 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:9 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:9 measurement http://www.ebi.ac.uk/efo/EFO_0010443 GCST90257315 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:8 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:8 measurement http://www.ebi.ac.uk/efo/EFO_0010442 GCST90257316 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:7 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:7 measurement http://www.ebi.ac.uk/efo/EFO_0010441 GCST90257317 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C58:6 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 58:6 measurement http://www.ebi.ac.uk/efo/EFO_0010440 GCST90257318 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C60:12 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 60:12 measurement http://www.ebi.ac.uk/efo/EFO_0010444 GCST90257319 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:0 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257320 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C14:0 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0010356 GCST90257321 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylcholine-A levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 phosphatidylcholine 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0010382 GCST90257322 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylcholine-B levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0010382 GCST90257323 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 phosphatidylcholine 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0010381 GCST90257324 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010380 GCST90257325 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010379 GCST90257326 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:0 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 36:0 measurement http://www.ebi.ac.uk/efo/EFO_0021473 GCST90257327 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:5 measurement http://www.ebi.ac.uk/efo/EFO_0010412 GCST90257278 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:3 measurement http://www.ebi.ac.uk/efo/EFO_0010410 GCST90257279 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:2 measurement http://www.ebi.ac.uk/efo/EFO_0010409 GCST90257280 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:4 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 phosphatidylcholine 34:4 measurement http://www.ebi.ac.uk/efo/EFO_0010378 GCST90257281 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:1 measurement http://www.ebi.ac.uk/efo/EFO_0010408 GCST90257282 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 50:0 measurement http://www.ebi.ac.uk/efo/EFO_0021480 GCST90257283 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C51:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257284 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C51:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 51:1 measurement http://www.ebi.ac.uk/efo/EFO_0021482 GCST90257285 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:7 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257286 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C51:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 51:0 measurement http://www.ebi.ac.uk/efo/EFO_0021481 GCST90257287 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:4 measurement http://www.ebi.ac.uk/efo/EFO_0010416 GCST90257288 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:3 measurement http://www.ebi.ac.uk/efo/EFO_0010415 GCST90257289 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:2 measurement http://www.ebi.ac.uk/efo/EFO_0010414 GCST90257290 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 52:1 measurement http://www.ebi.ac.uk/efo/EFO_0010413 GCST90257291 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0010377 GCST90257292 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C52:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257293 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C53:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257294 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:9 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:9 measurement http://www.ebi.ac.uk/efo/EFO_0010427 GCST90257295 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C53:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 53:2 measurement http://www.ebi.ac.uk/efo/EFO_0021484 GCST90257296 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:8 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:8 measurement http://www.ebi.ac.uk/efo/EFO_0010426 GCST90257297 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:5 measurement http://www.ebi.ac.uk/efo/EFO_0010423 GCST90257298 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:4 measurement http://www.ebi.ac.uk/efo/EFO_0010422 GCST90257299 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:3 measurement http://www.ebi.ac.uk/efo/EFO_0010421 GCST90257300 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:2 measurement http://www.ebi.ac.uk/efo/EFO_0010420 GCST90257301 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C54:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 54:1 measurement http://www.ebi.ac.uk/efo/EFO_0010419 GCST90257302 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C18:0 Monoacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lipid measurement http://www.ebi.ac.uk/efo/EFO_0004529 GCST90257228 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C30:0 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 30:0 measurement http://www.ebi.ac.uk/efo/EFO_0020052 GCST90257229 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C32:2 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 32.2 measurement http://www.ebi.ac.uk/efo/EFO_0020055 GCST90257230 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C32:1 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257231 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C32:0 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0020054 GCST90257232 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:3 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:3 measurement http://www.ebi.ac.uk/efo/EFO_0020059 GCST90257233 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:2 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:2 measurement http://www.ebi.ac.uk/efo/EFO_0010353 GCST90257234 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:1 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:1 measurement http://www.ebi.ac.uk/efo/EFO_0010352 GCST90257235 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C34:0 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 34:0 measurement http://www.ebi.ac.uk/efo/EFO_0020058 GCST90257236 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C30:0 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C30:0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0801129 GCST90257237 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:4 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:4 measurement http://www.ebi.ac.uk/efo/EFO_0020063 GCST90257238 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:3 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:3 measurement http://www.ebi.ac.uk/efo/EFO_0020062 GCST90257239 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:2 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:2 measurement http://www.ebi.ac.uk/efo/EFO_0010355 GCST90257240 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:1 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 36:1 measurement http://www.ebi.ac.uk/efo/EFO_0010354 GCST90257241 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C36:0 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diglyceride measurement http://www.ebi.ac.uk/efo/EFO_0010223 GCST90257242 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C38:5 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 38:5 measurement http://www.ebi.ac.uk/efo/EFO_0020067 GCST90257243 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C38:4 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0020066 GCST90257244 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C38:4 Diacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 diacylglycerol 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0020066 GCST90257245 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C41:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257246 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C42:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257247 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:2 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 32:2 measurement http://www.ebi.ac.uk/efo/EFO_0010374 GCST90257248 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C43:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257249 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C43:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257250 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C44:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 NH4_C44:2 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801203 GCST90257251 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C44:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 NH4_C44:1 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801202 GCST90257252 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 38:6 measurement http://www.ebi.ac.uk/efo/EFO_0010388 GCST90257328 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 phosphatidylcholine 38:4 measurement http://www.ebi.ac.uk/efo/EFO_0010386 GCST90257329 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:3 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 38:3 measurement http://www.ebi.ac.uk/efo/EFO_0010385 GCST90257330 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:2 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 1 phosphatidylcholine 38:2 measurement http://www.ebi.ac.uk/efo/EFO_0010384 GCST90257331 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:1 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 16:1 measurement http://www.ebi.ac.uk/efo/EFO_0010358 GCST90257332 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:9 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257333 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C40:6 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 40:6 measurement http://www.ebi.ac.uk/efo/EFO_0010389 GCST90257334 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 hydroxy-Phosphatidylcholine-A levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257335 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 hydroxy-Phosphatidylcholine-B levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257336 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 hydroxy-Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257337 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:5 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257338 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:3 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C34:3 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801134 GCST90257339 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:2 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257340 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Phosphatidylcholine plasmalogen-A levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257341 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C34:1 Phosphatidylcholine plasmalogen-B levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257342 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C16:0 Lysophosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 lysophosphatidylcholine 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0010357 GCST90257343 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylcholine plasmalogen-A levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:5 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801141 GCST90257344 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:5 Phosphatidylcholine plasmalogen-B levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C36:5 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801141 GCST90257345 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:4 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257346 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:3 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257347 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:2 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257348 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C36:1 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257349 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:7 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:7 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801148 GCST90257350 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:6 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 C38:6 phosphatidylcholine plasmalogen measurement http://www.ebi.ac.uk/efo/EFO_0801145 GCST90257351 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C38:4 Phosphatidylcholine plasmalogen levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine measurement http://www.ebi.ac.uk/efo/EFO_0010226 GCST90257352 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257254 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257255 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257256 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C45:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257257 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257258 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:1 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 32:1 measurement http://www.ebi.ac.uk/efo/EFO_0010373 GCST90257259 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 NH4_C46:3 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801205 GCST90257260 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 NH4_C46:2 TAG measurement http://www.ebi.ac.uk/efo/EFO_0801204 GCST90257261 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 46:0 measurement http://www.ebi.ac.uk/efo/EFO_0010400 GCST90257262 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C46:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 46:0 measurement http://www.ebi.ac.uk/efo/EFO_0010400 GCST90257263 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C47:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257264 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C47:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257265 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C47:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257266 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:5 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257267 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:4 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:4 measurement http://www.ebi.ac.uk/efo/EFO_0010407 GCST90257268 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:2 measurement http://www.ebi.ac.uk/efo/EFO_0010405 GCST90257269 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. C32:0 Phosphatidylcholine levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 phosphatidylcholine 32:0 measurement http://www.ebi.ac.uk/efo/EFO_0010372 GCST90257270 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:1 measurement http://www.ebi.ac.uk/efo/EFO_0010404 GCST90257271 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C48:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 48:0 measurement http://www.ebi.ac.uk/efo/EFO_0010403 GCST90257272 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:3 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257273 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:2 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257274 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:1 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triacylglycerol 49:1 measurement http://www.ebi.ac.uk/efo/EFO_0021479 GCST90257275 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C49:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257276 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C50:6 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257277 Genome-wide genotyping array 2023-05-04 35120996 Rhee EP 2022-02-01 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35120996 Trans-ethnic genome-wide association study of blood metabolites in the chronic renal insufficiency cohort (CRIC) study. NH4_C44:0 Triacylglycerol levels in chronic kidney disease 822 European ancestry individuals NA Illumina [9097073] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90257253 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. S-warfarin levels 531 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 80 S-warfarin measurement http://www.ebi.ac.uk/efo/EFO_0803323 GCST90129562 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. R-warfarin levels 530 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 211 R-warfarin measurement http://www.ebi.ac.uk/efo/EFO_0803324 GCST90129563 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. RS-warfarin levels 524 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 102 RS-warfarin measurement http://www.ebi.ac.uk/efo/EFO_0803325 GCST90129564 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. S-6-hydroxywarfarin levels 260 Sub-Saharan African ancestry individuals NA Illumina [17259403] (imputed) 280 S-6-hydroxywarfarin measurement http://www.ebi.ac.uk/efo/EFO_0803326 GCST90129565 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. R-6-hydroxywarfarin levels 377 Sub-Saharan African ancestry individuals NA Illumina [17267937] (imputed) 94 R-6-hydroxywarfarin measurement http://www.ebi.ac.uk/efo/EFO_0803327 GCST90129566 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. RS-6-hydroxywarfarin levels 233 Sub-Saharan African ancestry individuals NA Illumina [17245627] (imputed) 132 RS-6-hydroxywarfarin measurement http://www.ebi.ac.uk/efo/EFO_0803328 GCST90129567 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. S-7-hydroxywarfarin levels 514 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 84 S-7-hydroxywarfarin measurement http://www.ebi.ac.uk/efo/EFO_0803329 GCST90129568 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. RS-10-hydroxywarfarin levels 492 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 78 RS-10-hydroxywarfarin measurement http://www.ebi.ac.uk/efo/EFO_0803330 GCST90129569 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. S-warfarin to R-warfarin ratio 524 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 79 S-warfarin to R-warfarin ratio measurement http://www.ebi.ac.uk/efo/EFO_0803331 GCST90129570 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. S-6-hydroxywarfarin to S-warfarin ratio 510 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 65 S-6-hydroxywarfarin to S-warfarin ratio measurement http://www.ebi.ac.uk/efo/EFO_0803332 GCST90129571 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. R-6-hydroxywarfarin to R-warfarin ratio 258 Sub-Saharan African ancestry individuals NA Illumina [17258720] (imputed) 77 R-6-hydroxywarfarin to R-warfarin ratio measurement http://www.ebi.ac.uk/efo/EFO_0803333 GCST90129572 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. S-7-hydroxywarfarin to S-warfarin ratio 369 Sub-Saharan African ancestry individuals NA Illumina [17267842] (imputed) 68 S-7-hydroxywarfarin to S-warfarin ratio measurement http://www.ebi.ac.uk/efo/EFO_0803334 GCST90129573 Genome-wide genotyping array 2023-01-06 36210801 Asiimwe IG 2022-09-23 Front Pharmacol www.ncbi.nlm.nih.gov/pubmed/36210801 A genome-wide association study of plasma concentrations of warfarin enantiomers and metabolites in sub-Saharan black-African patients. RS-10-hydroxywarfarin to RS-warfarin ratio 481 Sub-Saharan African ancestry individuals NA Illumina [17268054] (imputed) 90 RS-10-hydroxywarfarin to RS-warfarin ratio measurement http://www.ebi.ac.uk/efo/EFO_0803335 GCST90129574 Genome-wide genotyping array 2023-01-11 36228427 Yuan J 2022-10-08 Asian J Psychiatr www.ncbi.nlm.nih.gov/pubmed/36228427 Discovery of a genome-wide significant locus associated with antidepressant response in Han Chinese population. Response to antidepressants (symptom improvement) in major depressive disorder 724 Han Chinese ancestry individuals NA Illumina [8307703] (imputed) 13 depressive symptom measurement, response to antidepressant http://www.ebi.ac.uk/efo/EFO_0007006, http://purl.obolibrary.org/obo/GO_0036276 GCST90244558 Genome-wide genotyping array 2023-01-11 36228427 Yuan J 2022-10-08 Asian J Psychiatr www.ncbi.nlm.nih.gov/pubmed/36228427 Discovery of a genome-wide significant locus associated with antidepressant response in Han Chinese population. Response to antidepressants in major depressive disorder 465 Han Chinese ancestry cases, 259 Han Chinese ancestry controls NA Illumina [8307703] (imputed) 6 response to antidepressant http://purl.obolibrary.org/obo/GO_0036276 GCST90244559 Genome-wide genotyping array 2023-01-11 32894760 Zhang H 2020-09-07 J Natl Cancer Inst www.ncbi.nlm.nih.gov/pubmed/32894760 Association of GATA3 polymorphisms with minimal residual disease and relapse risk in childhood acute lymphoblastic leukemia. End-of-induction therapy minimal residual disease in childhood acute lymphoblastic leukemia 243 European ancestry cases, 1,181 European ancestry controls, 18 Black cases, 110 Black controls, 141 Hispanic cases, 531 Hispanic controls, 16 Asian ancestry cases, 54 Asian ancestry controls, 54 cases, 249 controls 49 European ancestry cases, 248 European ancestry controls, 4 Black cases, 29 Black controls, 23 Hispanic cases, 82 Hispanic controls, 3 Asian ancestry cases, 9 Asian ancestry controls, 3 cases, 41 controls Affymetrix [863370] (imputed) 0 response to combination chemotherapy http://www.ebi.ac.uk/efo/EFO_0007965 GCST90239827 Genome-wide genotyping array 2023-01-03 35554533 Gao G 2022-05-12 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/35554533 Polygenic Risk Scores for Prediction of Breast Cancer Risk in Women of African Ancestry: a Cross-Ancestry Approach. Breast cancer 8,336 African American or Afro-Caribbean cases, 8,554 African American or Afro-Caribbean controls, 899 Sub-Saharan African ancestry cases, 1,630 Sub-Saharan African ancestry controls NA Illumina [15000000] (imputed) 0 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90244101 Genome-wide genotyping array 2022-12-13 36352089 Mingardo E 2022-11-09 Commun Biol www.ncbi.nlm.nih.gov/pubmed/36352089 A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy. Classic bladder exstrophy 628 European ancestry cases, 7,352 European ancestry controls NA Illumina [8289003] (imputed) 8 bladder exstrophy http://purl.obolibrary.org/obo/MONDO_0010805 GCST90132313 Genome-wide genotyping array 2022-12-22 35793592 Juyal G 2022-07-03 J Ayurveda Integr Med www.ncbi.nlm.nih.gov/pubmed/35793592 Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS. Rheumatoid arthritis 229 Indian ancestry cases, 215 Indian ancestry controls NA Illumina [528461] 8 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90244058 Genome-wide genotyping array 2022-12-22 35793592 Juyal G 2022-07-03 J Ayurveda Integr Med www.ncbi.nlm.nih.gov/pubmed/35793592 Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS. Ayurvedic vata prakriti specific rheumatoid arthritis 45 Indian ancestry cases, 24 Indian ancestry controls NA Illumina [528461] 3 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90244059 Genome-wide genotyping array 2022-12-22 35793592 Juyal G 2022-07-03 J Ayurveda Integr Med www.ncbi.nlm.nih.gov/pubmed/35793592 Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS. Ayurvedic pitta prakriti specific rheumatoid arthritis 113 Indian ancestry cases, 131 Indian ancestry controls NA Illumina [528461] 7 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90244060 Genome-wide genotyping array 2022-12-22 35793592 Juyal G 2022-07-03 J Ayurveda Integr Med www.ncbi.nlm.nih.gov/pubmed/35793592 Stratification of rheumatoid arthritis cohort using Ayurveda based deep phenotyping approach identifies novel genes in a GWAS. Ayurvedic kapha prakriti specific rheumatoid arthritis 71 Indian ancestry cases, 60 Indian ancestry controls NA Illumina [528461] 3 rheumatoid arthritis http://www.ebi.ac.uk/efo/EFO_0000685 GCST90244061 Genome-wide genotyping array 2023-08-14 23754956 Grarup N 2013-06-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23754956 Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. Vitamin B12 levels 38,229 Danish, Icelandic ancestry individuals NA Illumina [NR] (imputed) 11 vitamin B12 measurement http://www.ebi.ac.uk/efo/EFO_0004620 GCST90277442 Genome-wide sequencing, Exome-wide sequencing 2023-08-14 23754956 Grarup N 2013-06-06 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/23754956 Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets. Serum folate levels 21,708 Danish, Icelandic ancestry individuals NA Illumina [NR] (imputed) 2 folic acid measurement http://www.ebi.ac.uk/efo/EFO_0005111 GCST90277443 Genome-wide sequencing, Exome-wide sequencing 2023-01-05 34976003 Lim CK 2021-12-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34976003 STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency. HLA risk haplotype in IgA deficiency 636 Swedish ancestry cases, 7,789 Swedish ancestry controls NA Illumina [572856] (imputed) 1 HLA allele carrier status http://www.ebi.ac.uk/efo/EFO_0803322 GCST90244122 Genome-wide genotyping array 2023-01-05 34976003 Lim CK 2021-12-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34976003 STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency. HLA risk haplotype in IgA deficiency (homozygous HLA-DRB1*07:01 HLA-DQB1*02:02) 7 Swedish ancestry cases, 30 Swedish ancestry controls NA Illumina [572856] (imputed) 3 HLA allele carrier status http://www.ebi.ac.uk/efo/EFO_0803322 GCST90244123 Genome-wide genotyping array 2023-01-05 34976003 Lim CK 2021-12-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34976003 STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency. HLA risk haplotype in IgA deficiency (homozygous HLA-DRB1*01 HLA-DQB1*05:01) 34 Swedish ancestry cases, 68 Swedish ancestry controls NA Illumina [572856] (imputed) 1 HLA allele carrier status http://www.ebi.ac.uk/efo/EFO_0803322 GCST90244124 Genome-wide genotyping array 2023-01-05 34976003 Lim CK 2021-12-17 Front Genet www.ncbi.nlm.nih.gov/pubmed/34976003 STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency. HLA risk haplotype in IgA deficiency (homozygous HLA-B*08:01 HLA-DRB1*03:01 HLA-DQB1*02:01) 68 Swedish ancestry cases, 123 Swedish ancestry controls NA Illumina [572856] (imputed) 0 HLA allele carrier status http://www.ebi.ac.uk/efo/EFO_0803322 GCST90244125 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Glycine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90244106 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Alanine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90244107 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Leucine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90244108 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Valine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90244109 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Isoleucine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90244110 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Pyruvate levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90244111 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Tyrosine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90244112 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Histidine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90244113 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Phenylalanine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90244114 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Glutamine levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90244115 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Acetone levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 acetone measurement http://www.ebi.ac.uk/efo/EFO_0010989 GCST90244116 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. 3-Hydroxybutyrate levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90244117 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Acetoacetate levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90244118 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Glucose levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90244119 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Lactate levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90244120 Genome-wide genotyping array 2023-01-05 36073519 Smith CJ 2022-09-08 Elife www.ncbi.nlm.nih.gov/pubmed/36073519 Integrative analysis of metabolite GWAS illuminates the molecular basis of pleiotropy and genetic correlation. Citrate levels 94,464 European ancestry individuals NA NR [NR] (imputed) 0 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90244121 Genome-wide genotyping array 2022-12-16 35533259 Giles J 2022-05-09 Blood Adv www.ncbi.nlm.nih.gov/pubmed/35533259 Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia. Platelet factor 4/heparin antibody levels in heparin treatment 4,986 European ancestry individuals NA Illumina [NR] (imputed) 13 response to heparin, antibody measurement http://www.ebi.ac.uk/efo/EFO_0006816, http://www.ebi.ac.uk/efo/EFO_0004556 GCST90244012 Genome-wide genotyping array 2023-01-04 36065883 Kim C 2022-09-01 Physiol Rep www.ncbi.nlm.nih.gov/pubmed/36065883 Lung- and liver-dominant phenotypes of Korean eight constitution medicine have different profiles of genotype associated with each organ function. Korean Eight Constitution Medicine type (Hepatonia and Pulmotonia) 63 Korean ancestry individuals NA NR [304512] 0 hepatonia constitution type, pulmotonia constitution type http://www.ebi.ac.uk/efo/EFO_0022051, http://www.ebi.ac.uk/efo/EFO_0022050 GCST90179131 Genome-wide genotyping array 2023-01-10 36208799 Larsson SC 2022-10-05 Metabolism www.ncbi.nlm.nih.gov/pubmed/36208799 Genome-wide association and Mendelian randomization study of fibroblast growth factor 21 reveals causal associations with hyperlipidemia and possibly NASH. Circulating fibroblast growth factor 21 levels 6,259 Swedish ancestry individuals 4,483 Swedish ancestry women Illumina [7800000] (imputed) 2 fibroblast growth factor 21 measurement http://www.ebi.ac.uk/efo/EFO_0010783 GCST90244190 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes 38,965 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 7 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90205200 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes 38,965 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 6 abdominal adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803316 GCST90205201 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Gluteofemoral adipose tissue volumes 38,965 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 27 gluteofemoral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803317 GCST90205202 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes (adjusted for BMI and height) 37,641 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 30 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90205203 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes (adjusted for BMI and height) 37,641 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 21 abdominal adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803316 GCST90205204 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Gluteofemoral adipose tissue volumes (adjusted for BMI and height) 37,641 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 54 gluteofemoral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803317 GCST90205205 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes to abdominal adipose tissue volumes ratio 38,965 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 33 visceral:abdominal adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803318 GCST90205206 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes to gluteofemoral adipose tissue volumes ratio 38,965 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 30 visceral:gluteofemoral adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803319 GCST90205207 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes to gluteofemoral adipose tissue volumes ratio 38,965 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry individuals NA Affymetrix [11485690] (imputed) 17 abdominal:gluteofemoral adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803320 GCST90205208 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes 19,872 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 1 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90205209 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes 19,872 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 1 abdominal adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803316 GCST90205210 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Gluteofemoral adipose tissue volumes 19,872 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 2 gluteofemoral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803317 GCST90205211 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes (adjusted for BMI and height) 18,368 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 11 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90205212 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes (adjusted for BMI and height) 18,368 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 8 abdominal adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803316 GCST90205213 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Gluteofemoral adipose tissue volumes (adjusted for BMI and height) 18,368 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 12 gluteofemoral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803317 GCST90205214 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes to abdominal adipose tissue volumes ratio 18,984 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 16 visceral:abdominal adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803318 GCST90205215 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes to gluteofemoral adipose tissue volumes ratio 18,984 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 9 visceral:gluteofemoral adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803319 GCST90205216 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes to gluteofemoral adipose tissue volumes ratio 18,984 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry males NA Affymetrix [11485690] (imputed) 2 abdominal:gluteofemoral adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803320 GCST90205217 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes 19,093 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 2 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90205218 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes 19,093 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 1 abdominal adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803316 GCST90205219 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Gluteofemoral adipose tissue volumes 19,093 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 6 gluteofemoral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803317 GCST90205220 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes (adjusted for BMI and height) 19,273 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 16 visceral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0004765 GCST90205221 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes (adjusted for BMI and height) 19,273 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 8 abdominal adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803316 GCST90205222 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Gluteofemoral adipose tissue volumes (adjusted for BMI and height) 19,273 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 31 gluteofemoral adipose tissue measurement http://www.ebi.ac.uk/efo/EFO_0803317 GCST90205223 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes to abdominal adipose tissue volumes ratio 19,981 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 13 visceral:abdominal adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803318 GCST90205224 Genome-wide genotyping array 2023-01-05 35021295 Wang F 2022-01-01 World J Mens Health www.ncbi.nlm.nih.gov/pubmed/35021295 Genome-Wide Association Analysis to Search for New Loci Associated with Lifelong Premature Ejaculation Risk in Chinese Male Han Population. Lifelong premature ejaculation 120 Han Chinese ancestry cases, 366 Han Chinese ancestry controls NA Affymetrix [4572568] (imputed) 10 premature ejaculation http://www.ebi.ac.uk/efo/EFO_0803321 GCST90102431 Genome-wide genotyping array 2023-01-24 36627639 Jin H 2023-01-11 BMC Med www.ncbi.nlm.nih.gov/pubmed/36627639 Identification of genetic variants associated with diabetic kidney disease in multiple Korean cohorts via a genome-wide association study mega-analysis. Diabetic kidney disease 2,532 Korean ancestry cases, 31,347 Korean ancestry controls NA Affymetrix [4872923] (imputed) 5 diabetic nephropathy http://www.ebi.ac.uk/efo/EFO_0000401 GCST90179152 Genome-wide genotyping array 2023-02-02 36510243 Ko CL 2022-12-12 J Transl Med www.ncbi.nlm.nih.gov/pubmed/36510243 Genome-wide association study reveals ethnicity-specific SNPs associated with ankylosing spondylitis in the Taiwanese population. Ankylosing spondylitis 206 Taiwanese ancestry cases, 1,236 Taiwanese ancestry controls NA NR [NR] 0 ankylosing spondylitis http://www.ebi.ac.uk/efo/EFO_0003898 GCST90245872 Genome-wide genotyping array 2022-12-14 34533693 Huang L 2021-09-17 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34533693 Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Free triiodothyronine (T3) levels 124 Han Chinese ancestry individuals 313 Han Chinese ancestry individuals NR [6423076] (imputed) 0 triiodothyronine measurement http://www.ebi.ac.uk/efo/EFO_0008392 GCST90044908 Genome-wide genotyping array 2022-12-14 34533693 Huang L 2021-09-17 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34533693 Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Triiodothyronine levels 124 Han Chinese ancestry individuals 313 Han Chinese ancestry individuals NR [6423076] (imputed) 0 triiodothyronine measurement http://www.ebi.ac.uk/efo/EFO_0008392 GCST90044909 Genome-wide genotyping array 2022-12-14 34533693 Huang L 2021-09-17 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34533693 Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Thyroxine levels 124 Han Chinese ancestry individuals 313 Han Chinese ancestry individuals NR [6423076] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90044910 Genome-wide genotyping array 2022-12-14 34533693 Huang L 2021-09-17 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34533693 Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Thyroglobulin levels 124 Han Chinese ancestry individuals 313 Han Chinese ancestry individuals NR [6423076] (imputed) 0 thyroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0010050 GCST90044911 Genome-wide genotyping array 2022-12-14 34533693 Huang L 2021-09-17 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34533693 Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Thyroid peroxidase antibody levels 124 Han Chinese ancestry individuals 313 Han Chinese ancestry individuals NR [6423076] (imputed) 0 thyroid peroxidase antibody measurement http://www.ebi.ac.uk/efo/EFO_0005666 GCST90044912 Genome-wide genotyping array 2022-12-14 34533693 Huang L 2021-09-17 Genes Genomics www.ncbi.nlm.nih.gov/pubmed/34533693 Preliminary study of genome-wide association identified novel susceptibility genes for thyroid-related hormones in Chinese population. Thyroid stimulating hormone levels 124 Han Chinese ancestry individuals 313 Han Chinese ancestry individuals NR [6423076] (imputed) 0 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST90044913 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. BMI in smokers 79,703 European ancestry individuals NA NR [2375325] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244062 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. BMI in non-smokers 465,428 European ancestry individuals NA NR [2375325] (imputed) 0 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244063 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. Body mass index 545,131 European ancestry individuals NA NR [2375325] (imputed) 2 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90244064 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. Waist circumference adjusted for BMI in smokers 79,703 European ancestry individuals NA NR [2375325] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90244065 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. Waist circumference adjusted for BMI in non-smokers 465,428 European ancestry individuals NA NR [2375325] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90244066 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. Waist circumference adjusted for body mass index 545,131 European ancestry individuals NA NR [2375325] (imputed) 0 BMI-adjusted waist circumference http://www.ebi.ac.uk/efo/EFO_0007789 GCST90244067 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. Waist-to-hip ratio adjusted for BMI in smokers 79,703 European ancestry individuals NA NR [2375325] (imputed) 0 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90244068 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. Waist-to-hip ratio adjusted for BMI in non-smokers 465,428 European ancestry individuals NA NR [2375325] (imputed) 2 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90244069 Genome-wide genotyping array 2022-12-22 35793639 Lee WJ 2022-07-06 Lifestyle Genom www.ncbi.nlm.nih.gov/pubmed/35793639 Smoking-interaction loci affect obesity traits: a gene-smoking stratified meta-analysis of 545,131 Europeans. Waist-to-hip ratio adjusted for BMI 545,131 European ancestry individuals NA NR [2375325] (imputed) 2 BMI-adjusted waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0007788 GCST90244070 Genome-wide genotyping array 2022-12-16 35652242 Mykkanen AJH 2022-06-02 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35652242 Genome-wide association study of simvastatin pharmacokinetics. AUC of simvastatin lactone 170 European ancestry individuals NA Illumina [261030] 0 response to simvastatin http://purl.obolibrary.org/obo/GO_1903491 GCST90244015 Genome-wide genotyping array 2022-12-16 35652242 Mykkanen AJH 2022-06-02 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35652242 Genome-wide association study of simvastatin pharmacokinetics. AUC of simvastatin acid 170 European ancestry individuals NA Illumina [261030] 1 response to simvastatin http://purl.obolibrary.org/obo/GO_1903491 GCST90244016 Genome-wide genotyping array 2022-12-16 35652242 Mykkanen AJH 2022-06-02 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35652242 Genome-wide association study of simvastatin pharmacokinetics. AUC of 3',5'-dihydrodiol simvastatin lactone 170 European ancestry individuals NA Illumina [261030] 0 response to simvastatin http://purl.obolibrary.org/obo/GO_1903491 GCST90244017 Genome-wide genotyping array 2022-12-16 35652242 Mykkanen AJH 2022-06-02 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35652242 Genome-wide association study of simvastatin pharmacokinetics. AUC of 3',5'-dihydrodiol simvastatin acid 170 European ancestry individuals NA Illumina [261030] 0 response to simvastatin http://purl.obolibrary.org/obo/GO_1903491 GCST90244018 Genome-wide genotyping array 2022-12-16 35652242 Mykkanen AJH 2022-06-02 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35652242 Genome-wide association study of simvastatin pharmacokinetics. AUC of 3'-hydroxy simvastatin acid 170 European ancestry individuals NA Illumina [261030] 0 response to simvastatin http://purl.obolibrary.org/obo/GO_1903491 GCST90244019 Genome-wide genotyping array 2022-12-16 35652242 Mykkanen AJH 2022-06-02 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35652242 Genome-wide association study of simvastatin pharmacokinetics. AUC of simvastatin lactone 229 European ancestry individuals NA Illumina [136688] 0 response to simvastatin http://purl.obolibrary.org/obo/GO_1903491 GCST90244020 Genome-wide genotyping array 2022-12-16 35652242 Mykkanen AJH 2022-06-02 Clin Pharmacol Ther www.ncbi.nlm.nih.gov/pubmed/35652242 Genome-wide association study of simvastatin pharmacokinetics. AUC of simvastatin acid 229 European ancestry individuals NA Illumina [136688] 1 response to simvastatin http://purl.obolibrary.org/obo/GO_1903491 GCST90244021 Genome-wide genotyping array 2023-01-05 36311265 Pillalamarri V 2022-09-26 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36311265 Whole-exome sequencing in 415,422 individuals identifies rare variants associated with mitochondrial DNA copy number. Mitochondrial DNA copy number 415,422 European ancestry individuals NA NR [26645252] 11 mitochondrial DNA measurement http://www.ebi.ac.uk/efo/EFO_0006312 GCST90244129 Exome-wide sequencing 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C42:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C42:3 measurement http://www.ebi.ac.uk/efo/EFO_0801310 GCST90240090 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C42:4 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C42:4 measurement http://www.ebi.ac.uk/efo/EFO_0801311 GCST90240091 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C42:5 levels 6,606 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C42:5 measurement http://www.ebi.ac.uk/efo/EFO_0801312 GCST90240092 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C44:3 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C44:3 measurement http://www.ebi.ac.uk/efo/EFO_0801313 GCST90240093 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C44:4 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 phosphatidylcholine acyl-alkyl C44:4 measurement http://www.ebi.ac.uk/efo/EFO_0801314 GCST90240094 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C44:5 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C44:5 measurement http://www.ebi.ac.uk/efo/EFO_0801315 GCST90240095 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phosphatidylcholine acyl-alkyl C44:6 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phosphatidylcholine acyl-alkyl C44:6 measurement http://www.ebi.ac.uk/efo/EFO_0801316 GCST90240096 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Phenylalanine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90240097 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Proline levels 7,475 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90240098 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Serine levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 3 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST002966 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C16:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 sphingomyeline C16:0 measurement http://www.ebi.ac.uk/efo/EFO_0801317 GCST002964 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C16:1 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 sphingomyeline C16:1 measurement http://www.ebi.ac.uk/efo/EFO_0801318 GCST90240101 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C18:0 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 sphingomyeline C18:0 measurement http://www.ebi.ac.uk/efo/EFO_0801319 GCST90240102 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C18:1 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 2 sphingomyeline C18:1 measurement http://www.ebi.ac.uk/efo/EFO_0801320 GCST90240103 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C20:2 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 sphingomyeline C20:2 measurement http://www.ebi.ac.uk/efo/EFO_0801321 GCST90240104 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C24:0 levels 7,477 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 sphingomyeline C24:0 measurement http://www.ebi.ac.uk/efo/EFO_0801322 GCST90240105 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C24:1 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 sphingomyeline C24:1 measurement http://www.ebi.ac.uk/efo/EFO_0801323 GCST90240106 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C26:0 levels 6,569 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 sphingomyeline C26:0 measurement http://www.ebi.ac.uk/efo/EFO_0801324 GCST90240107 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Sphingomyeline C26:1 levels 7,473 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 sphingomyeline C26:1 measurement http://www.ebi.ac.uk/efo/EFO_0801325 GCST90240108 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hydroxysphingomyeline C14:1 levels 7,478 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 hydroxysphingomyeline C14:1 measurement http://www.ebi.ac.uk/efo/EFO_0801326 GCST90240109 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hydroxysphingomyeline C16:1 levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 hydroxysphingomyeline C16:1 measurement http://www.ebi.ac.uk/efo/EFO_0801327 GCST90240110 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hydroxysphingomyeline C22:1 levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 hydroxysphingomyeline C22:1 measurement http://www.ebi.ac.uk/efo/EFO_0801328 GCST90240111 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hydroxysphingomyeline C22:2 levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 hydroxysphingomyeline C22:2 measurement http://www.ebi.ac.uk/efo/EFO_0801329 GCST90240112 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Hydroxysphingomyeline C24:1 levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 hydroxysphingomyeline C24:1 measurement http://www.ebi.ac.uk/efo/EFO_0801330 GCST90240113 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Threonine levels 5,666 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90240114 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Tryptophan levels 5,666 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90240115 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Tyrosine levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 1 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90240116 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Valine levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90240117 Genome-wide genotyping array 2022-12-13 26068415 Draisma HHM 2015-06-12 Nat Commun www.ncbi.nlm.nih.gov/pubmed/26068415 Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Leucine or isoleucine levels 6,538 European ancestry individuals 1,182 European ancestry individuals Affymetrix, Illumina [NR] (imputed) 0 leucine measurement, isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009770, http://www.ebi.ac.uk/efo/EFO_0009793 GCST90240118 Genome-wide genotyping array 2023-01-10 36275661 Song K 2022-10-03 Front Immunol www.ncbi.nlm.nih.gov/pubmed/36275661 Genome-wide association study of SNP- and gene-based approaches to identify susceptibility candidates for lupus nephritis in the Han Chinese population. Lupus nephritis in systemic lupus erythematosus 592 Han Chinese ancestry cases, 453 Han Chinese ancestry controls 188 cases, 171 controls Illumina [14076911] (imputed) 1 lupus nephritis http://www.ebi.ac.uk/efo/EFO_0005761 GCST90244184 Genome-wide genotyping array 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 4,605 African ancestry individuals 6,644 African American individuals NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245791 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 3,154 African ancestry women 3,732 African American women NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245792 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 1,451 African ancestry men 2,912 African American men NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245793 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 4,605 African ancestry individuals, 15,849 European ancestry individuals 6,644 African American individuals, 9,774 European ancestry individuals NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245794 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 15,849 European ancestry individuals 9,774 European ancestry individuals NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245795 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 8,870 European ancestry women 4,642 European ancestry women NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245796 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 6,979 European ancestry men 5,132 European ancestry men NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245797 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 3,154 African ancestry women, 8,870 European ancestry women 3,732 African American women, 4,642 European ancestry women NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245798 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Body mass index 1,451 African ancestry men, 6,979 European ancestry men 2,912 African American men, 5,132 European ancestry men NR [88168] 0 lean body mass http://www.ebi.ac.uk/efo/EFO_0004995 GCST90245799 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 4,899 African ancestry individuals 6,644 African American individuals NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245800 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 3,336 African ancestry women 3,732 African American women NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245801 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 1,563 African ancestry men 2,912 African American men NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245802 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 4,899 African ancestry individuals, 17,105 European ancestry individuals 6,644 African American individuals, 9,774 European ancestry individuals NR [455318] 2 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245803 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 17,105 European ancestry individuals 9,774 European ancestry individuals NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245804 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 9,430 European ancestry women 4,642 European ancestry women NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245805 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 7,675 European ancestry men 5,132 European ancestry men NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245806 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 3,336 African ancestry women, 9,430 European ancestry women 3,732 African American women, 4,642 European ancestry women NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245807 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Height 1,563 African ancestry men, 7,675 European ancestry men 2,912 African American men, 5,132 European ancestry men NR [455318] 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245808 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 4,294 African ancestry individuals 3,547 African American individuals NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245809 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 2,987 African ancestry women 2,308 African American women NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245810 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 1,307 African ancestry men 1,239 African American men NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245811 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 4,294 African ancestry individuals, 15,503 European ancestry individuals 1,229 European ancestry individuals, 3,547 African American individuals NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245812 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 15,503 European ancestry individuals 1,229 European ancestry individuals NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245813 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 8,678 European ancestry women 771 European ancestry women NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245814 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 6,825 European ancestry men 758 European ancestry men NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245815 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 2,987 African ancestry women, 8,678 European ancestry women 771 European ancestry women, 2,308 African American women NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245816 Exome-wide sequencing 2023-01-31 36568030 Young KL 2022-11-25 HGG Adv www.ncbi.nlm.nih.gov/pubmed/36568030 Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. Waist-hip ratio 1,307 African ancestry men, 6,825 European ancestry men 758 European ancestry men, 1,239 African American men NR [67633] 0 waist-hip ratio http://www.ebi.ac.uk/efo/EFO_0004343 GCST90245817 Exome-wide sequencing 2022-12-06 33767297 Chen C 2021-03-25 Sci Rep www.ncbi.nlm.nih.gov/pubmed/33767297 CPNE3 moderates the association between anxiety and working memory. Working memory x anxiety interaction 1,115 Han Chinese ancestry individuals NA Illumina [4856474] (imputed) 1 anxiety, short-term memory http://www.ebi.ac.uk/efo/EFO_0005230, http://www.ebi.ac.uk/efo/EFO_0004335 GCST90239853 Genome-wide genotyping array 2023-01-25 36344522 Jia G 2022-11-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36344522 Discerning asthma endotypes through comorbidity mapping. Asthma in any disease 44,383 European ancestry cases, 260,715 European ancestry controls 4,854 European ancestry cases, 33,806 European ancestry controls, 998 Caribbean ancestry cases, 5,835 Caribbean ancestry controls, 3,368 East Asian ancestry cases, 191,045 East Asian ancestry controls NR [96000000] (imputed) 103 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90244761 Genome-wide genotyping array 2023-01-25 36344522 Jia G 2022-11-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36344522 Discerning asthma endotypes through comorbidity mapping. Asthma in gastrointestinal disease 44,383 European ancestry cases, 260,715 European ancestry controls 4,854 European ancestry cases, 33,806 European ancestry controls, 998 Caribbean ancestry cases, 5,835 Caribbean ancestry controls, 3,368 East Asian ancestry cases, 191,045 East Asian ancestry controls NR [96000000] (imputed) 11 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90244762 Genome-wide genotyping array 2023-01-25 36344522 Jia G 2022-11-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36344522 Discerning asthma endotypes through comorbidity mapping. Asthma in lymphoma 44,383 European ancestry cases, 260,715 European ancestry controls 4,854 European ancestry cases, 33,806 European ancestry controls, 998 Caribbean ancestry cases, 5,835 Caribbean ancestry controls, 3,368 East Asian ancestry cases, 191,045 East Asian ancestry controls NR [96000000] (imputed) 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90244763 Genome-wide genotyping array 2023-01-25 36344522 Jia G 2022-11-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36344522 Discerning asthma endotypes through comorbidity mapping. Asthma in muscoskeletal disease 44,383 European ancestry cases, 260,715 European ancestry controls 4,854 European ancestry cases, 33,806 European ancestry controls, 998 Caribbean ancestry cases, 5,835 Caribbean ancestry controls, 3,368 East Asian ancestry cases, 191,045 East Asian ancestry controls NR [96000000] (imputed) 3 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90244764 Genome-wide genotyping array 2023-01-25 36344522 Jia G 2022-11-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36344522 Discerning asthma endotypes through comorbidity mapping. Asthma in cardiovascular disease 44,383 European ancestry cases, 260,715 European ancestry controls 4,854 European ancestry cases, 33,806 European ancestry controls, 998 Caribbean ancestry cases, 5,835 Caribbean ancestry controls, 3,368 East Asian ancestry cases, 191,045 East Asian ancestry controls NR [96000000] (imputed) 9 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90244765 Genome-wide genotyping array 2023-01-25 36344522 Jia G 2022-11-07 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36344522 Discerning asthma endotypes through comorbidity mapping. Asthma in lung disease 44,383 European ancestry cases, 260,715 European ancestry controls 4,854 European ancestry cases, 33,806 European ancestry controls, 998 Caribbean ancestry cases, 5,835 Caribbean ancestry controls, 3,368 East Asian ancestry cases, 191,045 East Asian ancestry controls NR [96000000] (imputed) 1 asthma http://purl.obolibrary.org/obo/MONDO_0004979 GCST90244766 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Visceral adipose tissue volumes to gluteofemoral adipose tissue volumes ratio 19,981 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 13 visceral:gluteofemoral adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803319 GCST90205225 Genome-wide genotyping array 2023-01-04 35773277 Agrawal S 2022-06-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35773277 Inherited basis of visceral, abdominal subcutaneous and gluteofemoral fat depots. Abdominal adipose tissue volumes to gluteofemoral adipose tissue volumes ratio 19,981 European ancestry, East Asian ancestry, South Asian ancestry, African ancestry, NR ancestry females NA Affymetrix [11485690] (imputed) 9 abdominal:gluteofemoral adipose tissue ratio measurement http://www.ebi.ac.uk/efo/EFO_0803320 GCST90205226 Genome-wide genotyping array 2022-12-08 34575070 Upadhyai P 2021-09-05 Life (Basel) www.ncbi.nlm.nih.gov/pubmed/34575070 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent. COVID-19 severity (severe vs asymptomatic) 1,492 European ancestry cases, 197 European ancestry controls NA NR [600569] 0 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90044898 Genome-wide genotyping array 2022-12-08 34575070 Upadhyai P 2021-09-05 Life (Basel) www.ncbi.nlm.nih.gov/pubmed/34575070 Genomic and Ancestral Variation Underlies the Severity of COVID-19 Clinical Manifestation in Individuals of European Descent. COVID-19 severity (severe vs asymptomatic) 1,492 European ancestry cases, 197 European ancestry controls NA NR [600569] 0 COVID-19 symptoms measurement http://www.ebi.ac.uk/efo/EFO_0600019 GCST90044899 Genome-wide genotyping array 2023-08-21 37038335 Brown AL 2023-04-11 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/37038335 Genetic susceptibility to cognitive decline following craniospinal irradiation for pediatric central nervous system tumors. Change in intelligence quotient in pediatric CNS tumors treated with craniospinal irradiation 150 European ancestry individuals 73 Asian ancestry, African ancestry, Hispanic or Latin American individuals Illumina [7983116] (imputed) 17 intelligence, response to cranial radiation therapy http://www.ebi.ac.uk/efo/EFO_0004337, http://www.ebi.ac.uk/efo/EFO_0010950 GCST90277984 Genome-wide genotyping array 2023-08-21 37038335 Brown AL 2023-04-11 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/37038335 Genetic susceptibility to cognitive decline following craniospinal irradiation for pediatric central nervous system tumors. Change in working memory in pediatric CNS tumors treated with craniospinal irradiation 129 European ancestry individuals 54 Asian ancestry, African ancestry, Hispanic or Latin American individuals Illumina [7983116] (imputed) 37 response to cranial radiation therapy, short-term memory http://www.ebi.ac.uk/efo/EFO_0010950, http://www.ebi.ac.uk/efo/EFO_0004335 GCST90277985 Genome-wide genotyping array 2023-08-21 37038335 Brown AL 2023-04-11 Neuro Oncol www.ncbi.nlm.nih.gov/pubmed/37038335 Genetic susceptibility to cognitive decline following craniospinal irradiation for pediatric central nervous system tumors. Change in processing speed in pediatric CNS tumors treated with craniospinal irradiation 133 European ancestry individuals 58 Asian ancestry, African ancestry, Hispanic or Latin American individuals Illumina [7983116] (imputed) 37 information processing speed, response to cranial radiation therapy http://www.ebi.ac.uk/efo/EFO_0004363, http://www.ebi.ac.uk/efo/EFO_0010950 GCST90277986 Genome-wide genotyping array 2022-12-22 35730328 Cheng B 2022-06-22 Eur Psychiatry www.ncbi.nlm.nih.gov/pubmed/35730328 Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression. Self-reported depression (with anxiety score <5) 59,334 European ancestry cases, 19,805 European ancestry controls NA Affymetrix [NR] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90244040 Genome-wide genotyping array 2022-12-22 35730328 Cheng B 2022-06-22 Eur Psychiatry www.ncbi.nlm.nih.gov/pubmed/35730328 Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression. Depression (with anxiety score <5) 59,334 European ancestry cases, 19,805 European ancestry controls NA Affymetrix [NR] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90244041 Genome-wide genotyping array 2022-12-22 35730328 Cheng B 2022-06-22 Eur Psychiatry www.ncbi.nlm.nih.gov/pubmed/35730328 Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression. Self-reported depression (with non-self-reported anxiety) 56,603 European ancestry cases, 13,123 European ancestry controls NA Affymetrix [NR] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90244042 Genome-wide genotyping array 2022-12-22 35730328 Cheng B 2022-06-22 Eur Psychiatry www.ncbi.nlm.nih.gov/pubmed/35730328 Genome-wide association studies in non-anxiety individuals identified novel risk loci for depression. Depression (with non-self-reported anxiety) 56,603 European ancestry cases, 13,123 European ancestry controls NA Affymetrix [NR] (imputed) 1 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90244043 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Methionine levels 7,795 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90243427 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Malate levels 7,384 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90243428 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Palmitate 16:0 levels 7,800 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90243429 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Nonadecanoate 19:0 levels 7,783 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90243430 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Stearate 18:0 levels 7,803 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90243431 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Oleate 18:1n9 levels 7,768 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 oleate 18:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021070 GCST90243432 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pentadecanoate 15:0 levels 7,502 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pentadecanoate 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021073 GCST90243433 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Myristate 14:0 levels 7,811 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90243434 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pipecolate levels 7,792 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90243435 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Ornithine levels 7,746 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90243436 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 5-oxoproline levels 7,802 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90243437 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pantothenate levels 7,604 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90243438 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Salicylate levels 2,374 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90243439 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-acetamidobutanoate levels 6,930 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90243440 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Alpha-tocopherol levels 7,725 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90243441 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Citrate levels 7,813 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90243442 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycerate levels 7,778 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90243443 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Guanosine levels 2,343 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 guanosine measurement http://www.ebi.ac.uk/efo/EFO_0021124 GCST90243444 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. N-acetylalanine levels 7,720 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90243445 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Urate levels 7,819 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90243446 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Ursodeoxycholate levels 5,477 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90243447 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Arginine levels 7,528 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 L-arginine measurement http://www.ebi.ac.uk/efo/EFO_0006524 GCST90243448 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Ascorbate (vitamin c) levels 2,085 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 vitamin C measurement http://www.ebi.ac.uk/efo/EFO_0600003 GCST90243449 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Caprate 10:0 levels 7,799 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 caprate 10:0 measurement http://www.ebi.ac.uk/efo/EFO_0021101 GCST90243450 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Heptanoate 7:0 levels 7,802 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 heptanoate 7:0 measurement http://www.ebi.ac.uk/efo/EFO_0021104 GCST90243451 Genome-wide genotyping array 2022-12-08 35680011 Pandit R 2022-06-06 Genomics www.ncbi.nlm.nih.gov/pubmed/35680011 First report on genome wide association study in western Indian population reveals host genetic factors for COVID-19 severity and outcome. Mortality in COVID-19 94 western Indian ancestry deceased cases, 317 western Indian ancestry recovered cases NA NR [6332698] (imputed) 29 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90239858 Genome-wide genotyping array 2022-12-08 35680011 Pandit R 2022-06-06 Genomics www.ncbi.nlm.nih.gov/pubmed/35680011 First report on genome wide association study in western Indian population reveals host genetic factors for COVID-19 severity and outcome. Morbidity in COVID-19 (deceased vs asymptomatic) 94 western Indian ancestry deceased cases, 147 western Indian ancestry asymptomatic cases NA NR [6468284] (imputed) 28 COVID-19, mortality http://purl.obolibrary.org/obo/MONDO_0100096, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90239859 Genome-wide genotyping array 2022-12-08 35680011 Pandit R 2022-06-06 Genomics www.ncbi.nlm.nih.gov/pubmed/35680011 First report on genome wide association study in western Indian population reveals host genetic factors for COVID-19 severity and outcome. COVID-19 (recovered vs asymptomatic) 317 western Indian ancestry recovered cases, 147 western Indian ancestry asymptomatic cases NA NR [NR] (imputed) 37 COVID-19 http://purl.obolibrary.org/obo/MONDO_0100096 GCST90239860 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Serine levels 7,796 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90243577 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Trans-4-hydroxyproline levels 7,802 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0010498 GCST90243578 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glutamate levels 7,804 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90243579 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hexanoylcarnitine levels 7,786 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90243580 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycine levels 7,802 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90243581 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Alanine levels 7,788 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90243582 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycochenodeoxycholate levels 7,087 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90243583 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-aminobutyrate levels 7,814 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90243584 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Scyllo-inositol levels 6,500 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 scyllo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0011001 GCST90243585 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Dodecanedioate levels 6,478 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90243586 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylvaline levels 7,753 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90243587 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Indolepropionate levels 7,803 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90243588 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Butyrylcarnitine levels 7,796 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 butyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020010 GCST90243589 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Myristoleate 14:1n5 levels 7,804 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90243590 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Dehydroisoandrosterone sulfate DHEA-S levels 7,793 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 dehydroisoandrosterone sulfate DHEA-S measurement http://www.ebi.ac.uk/efo/EFO_0021119 GCST90243591 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-methylxanthine levels 5,396 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90243592 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Propionylcarnitine levels 7,813 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 propionylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020942 GCST90243593 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Caproate 6:0 levels 7,811 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 caproate 6:0 measurement http://www.ebi.ac.uk/efo/EFO_0021102 GCST90243594 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Caprylate 8:0 levels 7,802 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 caprylate 8:0 measurement http://www.ebi.ac.uk/efo/EFO_0021103 GCST90243595 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 10-undecenoate (11:1n1) levels 7,806 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90243596 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Docosapentaenoate n3 DPA; 22:5n3 levels 7,821 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 docosapentaenoate n3 DPA; 22:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021048 GCST90243597 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-11204 levels 7,799 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-11204 measurement http://www.ebi.ac.uk/efo/EFO_0021219 GCST90243598 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-02269 levels 7,701 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-02269 measurement http://www.ebi.ac.uk/efo/EFO_0021183 GCST90243599 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phenol sulfate levels 7,810 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90243600 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-06126 levels 7,785 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-06126 measurement http://www.ebi.ac.uk/efo/EFO_0021197 GCST90243601 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Myo-inositol levels 7,803 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 inositol measurement http://www.ebi.ac.uk/efo/EFO_0010504 GCST90243527 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glucose levels 7,773 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90243528 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1,5-anhydroglucitol (1,5-ag) levels 7,746 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90243529 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Erythritol levels 7,776 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90243530 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-hydroxybutyrate AHB levels 7,815 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 2-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020999 GCST90243531 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-methyl-2-oxobutyrate levels 7,648 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90243532 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1,6-anhydroglucose levels 3,663 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1,6-anhydroglucose measurement http://www.ebi.ac.uk/efo/EFO_0021028 GCST90243533 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-palmitoylglycerol 1-monopalmitin levels 7,429 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-palmitoylglycerol 1-monopalmitin measurement http://www.ebi.ac.uk/efo/EFO_0021110 GCST90243534 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Saccharin levels 2,449 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 saccharin measurement http://www.ebi.ac.uk/efo/EFO_0021168 GCST90243535 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-oleoylglycerol 1-monoolein levels 5,717 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-oleoylglycerol 1-monoolein measurement http://www.ebi.ac.uk/efo/EFO_0021109 GCST90243536 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 1-stearoylglycerol (1-monostearin) levels 6,965 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 1-stearoylglycerol 1-monostearin measurement http://www.ebi.ac.uk/efo/EFO_0021111 GCST90243537 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-08402 levels 7,726 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 2 X-08402 measurement http://www.ebi.ac.uk/efo/EFO_0021205 GCST90243538 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 2-hydroxyisobutyrate levels 6,539 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010979 GCST90243539 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-08766 levels 6,050 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-08766 measurement http://www.ebi.ac.uk/efo/EFO_0021206 GCST90243540 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 4-methyl-2-oxopentanoate levels 7,776 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90243541 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phenyllactate (pla) levels 6,064 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 phenyllactate measurement http://www.ebi.ac.uk/efo/EFO_0021511 GCST90243542 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Homocitrulline levels 4,135 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90243543 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Aspartylphenylalanine levels 3,948 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 aspartylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0021127 GCST90243544 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Levulinate 4-oxovalerate levels 6,982 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 levulinate 4-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021024 GCST90243545 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Palmitoylcarnitine levels 7,701 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90243546 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-08988 levels 7,776 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 X-08988 measurement http://www.ebi.ac.uk/efo/EFO_0021207 GCST90243547 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-09026 levels 7,627 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-09026 measurement http://www.ebi.ac.uk/efo/EFO_0021208 GCST90243548 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-09108 levels 6,910 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-09108 measurement http://www.ebi.ac.uk/efo/EFO_0021209 GCST90243549 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cholate levels 5,929 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90243550 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-09706 levels 7,697 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-09706 measurement http://www.ebi.ac.uk/efo/EFO_0021210 GCST90243551 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Laurate (12:0) levels 7,793 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90243452 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Valine levels 7,808 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90243453 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Urea levels 7,796 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90243454 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cortisol levels 7,795 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90243455 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Cortisone levels 7,575 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90243456 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Proline levels 7,816 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90243457 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Citrulline levels 7,773 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90243458 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Biliverdin levels 6,686 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90243459 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Serotonin 5HT levels 6,139 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90243460 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamylglutamine levels 7,662 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90243461 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Gamma-glutamyltyrosine levels 7,468 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90243462 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Hypoxanthine levels 7,287 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 1 hypoxanthine mesurement http://www.ebi.ac.uk/efo/EFO_0010500 GCST90243463 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Betaine levels 7,806 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 4 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90243464 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Xanthine levels 6,845 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90243465 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Phosphate levels 7,789 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90243466 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. 3-methoxytyrosine levels 5,997 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90243467 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Pelargonate 9:0 levels 7,803 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 pelargonate 9:0 measurement http://www.ebi.ac.uk/efo/EFO_0021106 GCST90243468 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Undecanoate 11:0 levels 7,500 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 undecanoate 11:0 measurement http://www.ebi.ac.uk/efo/EFO_0021107 GCST90243469 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Beta-hydroxyisovalerate levels 7,283 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 3-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0010984 GCST90243470 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Taurodeoxycholate levels 1,564 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90243471 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-02973 levels 7,759 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-02973 measurement http://www.ebi.ac.uk/efo/EFO_0021184 GCST90243472 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-03003 levels 7,689 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-03003 measurement http://www.ebi.ac.uk/efo/EFO_0021185 GCST90243473 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-03088 levels 7,474 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 X-03088 measurement http://www.ebi.ac.uk/efo/EFO_0021187 GCST90243474 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. X-03094 levels 7,804 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 3 X-03094 measurement http://www.ebi.ac.uk/efo/EFO_0021188 GCST90243475 Genome-wide genotyping array 2022-12-09 24816252 Shin SY 2014-05-11 Nat Genet www.ncbi.nlm.nih.gov/pubmed/24816252 An atlas of genetic influences on human blood metabolites. Glycerol levels 7,800 European ancestry individuals NA Affymetrix, Illumina [2100000] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90243476 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Inflammatory bowel disease or major depressive disorder (pleiotropy) 7,045 European ancestry inflammatory bowel disease cases, 170,056 European ancestry major depressive disorder cases, 778,725 European ancestry controls NA NR [7361159] 7 unipolar depression, inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90271321 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Inflammatory bowel disease or schizophrenia (pleiotropy) 7,045 European ancestry inflammatory bowel disease cases, 40,675 European ancestry schizophrenia cases, 513,925 European ancestry controls NA NR [7078011] 6 schizophrenia, inflammatory bowel disease http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90271322 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Inflammatory bowel disease or bipolar disorder (pleiotropy) 7,045 European ancestry inflammatory bowel disease cases, 41,917 European ancestry bipolar disorder cases, 820,831 European ancestry controls NA NR [7130578] 5 schizophrenia, inflammatory bowel disease http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90271323 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Inflammatory bowel disease or anorexia nervosa (pleiotropy) 7,045 European ancestry inflammatory bowel disease cases, 16,992 European ancestry anorexia nervosa cases, 504,807 European ancestry controls NA NR [6839114] 2 schizophrenia, inflammatory bowel disease http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90271324 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Irritable bowel syndrome or major depressive disorder (pleiotropy) 53,400 European ancestry irritable bowel syndrome cases, 170,056 European ancestry major depressive disorder cases, 762,644 European ancestry controls NA NR [7496417] 7 unipolar depression, irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000555 GCST90271325 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Irritable bowel syndrome or posttraumatic stress disorder (pleiotropy) 53,400 European ancestry irritable bowel syndrome cases, 23,212 European ancestry PTSD cases, 584,648 European ancestry controls NA NR [7948182] 0 irritable bowel syndrome, post-traumatic stress disorder http://www.ebi.ac.uk/efo/EFO_0000555, http://www.ebi.ac.uk/efo/EFO_0001358 GCST90271326 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Irritable bowel syndrome or schizophrenia (pleiotropy) 53,400 European ancestry irritable bowel syndrome cases, 40,675 European ancestry schizophrenia cases, 497,844 European ancestry controls NA NR [7259187] 10 schizophrenia, irritable bowel syndrome http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0000555 GCST90271327 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Irritable bowel syndrome or attention-deficit/hyperactivity disorder (pleiotropy) 53,400 European ancestry irritable bowel syndrome cases, 19,099 European ancestry ADHD cases, 467,395 European ancestry controls NA NR [6844670] 2 attention deficit hyperactivity disorder, irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0000555 GCST90271328 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Irritable bowel syndrome or bipolar disorder (pleiotropy) 53,400 European ancestry irritable bowel syndrome cases, 41,917 European ancestry bipolar disorder cases, 804,750 European ancestry controls NA NR [7259266] 9 unipolar depression, irritable bowel syndrome http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0000555 GCST90271329 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Irritable bowel syndrome or anorexia nervosa (pleiotropy) 53,400 European ancestry irritable bowel syndrome cases, 16,992 European ancestry anorexia nervosa cases, 488,726 European ancestry controls NA NR [7061035] 2 irritable bowel syndrome, anorexia nervosa http://www.ebi.ac.uk/efo/EFO_0000555, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90271330 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Peptic ulcer disease or major depressive disorder (pleiotropy) 16,666 European ancestry peptic ulcer disease cases, 170,056 European ancestry major depressive disorder cases, 769,104 European ancestry controls NA NR [7361223] 0 peptic ulcer disease, unipolar depression http://purl.obolibrary.org/obo/MONDO_0004247, http://www.ebi.ac.uk/efo/EFO_0003761 GCST90271331 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Peptic ulcer disease or posttraumatic stress disorder (pleiotropy) 16,666 European ancestry peptic ulcer disease cases, 23,212 European ancestry PTSD cases, 591,108 European ancestry controls NA NR [7754811] 0 peptic ulcer disease, post-traumatic stress disorder http://purl.obolibrary.org/obo/MONDO_0004247, http://www.ebi.ac.uk/efo/EFO_0001358 GCST90271332 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Peptic ulcer disease or schizophrenia (pleiotropy) 16,666 European ancestry peptic ulcer disease cases, 40,675 European ancestry schizophrenia cases, 504,304 European ancestry controls NA NR [7078062] 4 peptic ulcer disease, schizophrenia http://purl.obolibrary.org/obo/MONDO_0004247, http://purl.obolibrary.org/obo/MONDO_0005090 GCST90271333 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Peptic ulcer disease or attention-deficit/hyperactivity disorder (pleiotropy) 16,666 European ancestry peptic ulcer disease cases, 19,099 European ancestry ADHD cases, 473,855 European ancestry controls NA NR [6845733] 3 attention deficit hyperactivity disorder, peptic ulcer disease http://www.ebi.ac.uk/efo/EFO_0003888, http://purl.obolibrary.org/obo/MONDO_0004247 GCST90271334 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Peptic ulcer disease or bipolar disorder (pleiotropy) 16,666 European ancestry peptic ulcer disease cases, 41,917 European ancestry bipolar disorder cases, 811,210 European ancestry controls NA NR [7130644] 4 peptic ulcer disease, bipolar disorder http://purl.obolibrary.org/obo/MONDO_0004247, http://purl.obolibrary.org/obo/MONDO_0004985 GCST90271335 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Peptic ulcer disease or anorexia nervosa (pleiotropy) 16,666 European ancestry peptic ulcer disease cases, 16,992 European ancestry anorexia nervosa cases, 495,186 European ancestry controls NA NR [6839179] 2 peptic ulcer disease, anorexia nervosa http://purl.obolibrary.org/obo/MONDO_0004247, http://purl.obolibrary.org/obo/MONDO_0005351 GCST90271336 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Gastroesophageal reflux disease or major depressive disorder (pleiotropy) 54,854 European ancestry gastroesophageal reflux disease cases, 170,056 European ancestry major depressive disorder cases, 730,916 European ancestry controls NA NR [7361223] 2 unipolar depression, gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90271337 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Gastroesophageal reflux disease or posttraumatic stress disorder (pleiotropy) 54,854 European ancestry gastroesophageal reflux disease cases, 23,212 European ancestry PTSD cases, 552,920 European ancestry controls NA NR [7754811] 1 post-traumatic stress disorder, gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0001358, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90271338 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Gastroesophageal reflux disease or schizophrenia (pleiotropy) 54,854 European ancestry gastroesophageal reflux disease cases, 40,675 European ancestry schizophrenia cases, 466,116 European ancestry controls NA NR [7078062] 9 schizophrenia, gastroesophageal reflux disease http://purl.obolibrary.org/obo/MONDO_0005090, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90271339 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Gastroesophageal reflux disease or attention-deficit/hyperactivity disorder (pleiotropy) 54,854 European ancestry gastroesophageal reflux disease cases, 19,099 European ancestry ADHD cases, 435,667 European ancestry controls NA NR [6845733] 2 attention deficit hyperactivity disorder, gastroesophageal reflux disease http://www.ebi.ac.uk/efo/EFO_0003888, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90271340 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Gastroesophageal reflux disease or bipolar disorder (pleiotropy) 54,854 European ancestry gastroesophageal reflux disease cases, 41,917 European ancestry bipolar disorder cases, 773,022 European ancestry controls NA NR [7130644] 2 bipolar disorder, gastroesophageal reflux disease http://purl.obolibrary.org/obo/MONDO_0004985, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90271341 Genome-wide genotyping array 2023-06-23 36753304 Gong W 2023-02-08 JAMA Psychiatry www.ncbi.nlm.nih.gov/pubmed/36753304 Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis. Gastroesophageal reflux disease or anorexia nervosa (pleiotropy) 54,854 European ancestry gastroesophageal reflux disease cases, 16,992 European ancestry anorexia nervosa cases, 456,998 European ancestry controls NA NR [6839179] 4 anorexia nervosa, gastroesophageal reflux disease http://purl.obolibrary.org/obo/MONDO_0005351, http://www.ebi.ac.uk/efo/EFO_0003948 GCST90271342 Genome-wide genotyping array 2023-08-01 36975205 Ahadi S 2023-03-28 Elife www.ncbi.nlm.nih.gov/pubmed/36975205 Longitudinal fundus imaging and its genome-wide association analysis provide evidence for a human retinal aging clock. Aging (eyeAgeAcceleration) 45,444 European ancestry individuals NA NR [13297147] (imputed) 38 obsolete aging http://purl.obolibrary.org/obo/GO_0007568 GCST90274864 Genome-wide genotyping array 2023-07-21 36980932 Bulgay C 2023-03-06 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36980932 Exome-Wide Association Study of Competitive Performance in Elite Athletes. Personal best scores in elite athletes 60 Turkish ancestry cases, 34 Turkish ancestry controls 488 Russian ancestry cases, 209 Russian ancestry controls Illumina [219232] 0 athletic endurance measurement http://www.ebi.ac.uk/efo/EFO_0007818 GCST90271726 Exome-wide sequencing 2023-08-02 37235137 Sun Z 2023-03-27 JHEP Rep www.ncbi.nlm.nih.gov/pubmed/37235137 Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals. Nonalcoholic fatty liver disease 6,623 European ancestry cases, 26,318 European ancestry controls NA NR [9740199] (imputed) 4 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90275041 Genome-wide genotyping array 2023-08-02 37235137 Sun Z 2023-03-27 JHEP Rep www.ncbi.nlm.nih.gov/pubmed/37235137 Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals. Nonalcoholic fatty liver disease in lean individuals (BMI <25) 810 European ancestry cases, 12,804 European ancestry controls NA NR [9740199] (imputed) 4 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90275044 Genome-wide genotyping array 2023-08-02 37235137 Sun Z 2023-03-27 JHEP Rep www.ncbi.nlm.nih.gov/pubmed/37235137 Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals. Nonalcoholic fatty liver disease in overweight individuals (25<=BMI<=30) 3,069 European ancestry cases, 10,641 European ancestry controls NA NR [9740199] (imputed) 4 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90275047 Genome-wide genotyping array 2023-08-02 37235137 Sun Z 2023-03-27 JHEP Rep www.ncbi.nlm.nih.gov/pubmed/37235137 Genetic variants in HFE are associated with non-alcoholic fatty liver disease in lean individuals. Nonalcoholic fatty liver disease in obese individuals (BMI>30) 2,744 European ancestry cases, 2,873 European ancestry controls NA NR [9740199] (imputed) 2 non-alcoholic fatty liver disease http://www.ebi.ac.uk/efo/EFO_0003095 GCST90275050 Genome-wide genotyping array 2023-07-12 36917350 Yao X 2023-03-14 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36917350 Genome-wide analysis of genetic pleiotropy and causal genes across three age-related ocular disorders. AMD or cataract or glaucoma (pleiotropy) 14,034 European ancestry AMD cases, 11,306 European ancestry cataract cases, 7,947 European ancestry glaucoma cases, 784,851 European ancestry controls NA NR [NR] 3 age-related macular degeneration, cataract, glaucoma http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0005129, http://purl.obolibrary.org/obo/MONDO_0005041 GCST90271893 Genome-wide genotyping array 2023-07-12 36917350 Yao X 2023-03-14 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36917350 Genome-wide analysis of genetic pleiotropy and causal genes across three age-related ocular disorders. Cataract or glaucoma (pleiotropy) 11,306 European ancestry cataract cases, 7,947 European ancestry glaucoma cases, 693,697 European ancestry controls NA NR [NR] 3 cataract, glaucoma http://purl.obolibrary.org/obo/MONDO_0005129, http://purl.obolibrary.org/obo/MONDO_0005041 GCST90271894 Genome-wide genotyping array 2023-07-12 36917350 Yao X 2023-03-14 Hum Genet www.ncbi.nlm.nih.gov/pubmed/36917350 Genome-wide analysis of genetic pleiotropy and causal genes across three age-related ocular disorders. AMD or glaucoma (pleiotropy) 14,034 European ancestry AMD cases, 7,947 European ancestry glaucoma cases, 434,963 European ancestry controls NA NR [NR] 1 age-related macular degeneration, glaucoma http://www.ebi.ac.uk/efo/EFO_0001365, http://purl.obolibrary.org/obo/MONDO_0005041 GCST90271895 Genome-wide genotyping array 2023-06-22 37212302 Qiu S 2023-05-01 J Med Virol www.ncbi.nlm.nih.gov/pubmed/37212302 Genetic correlation, causal relationship, and shared loci between vitamin D and COVID-19: A genome-wide cross-trait analysis. Vitamin D levels or COVID-19 (MTAG) 417,580 European ancestry individuals with vitamin D measurements, 38,984 European ancestry COVID-19 cases, 1,644,784 European ancestry controls NA NR [NR] 70 vitamin D measurement, COVID-19 http://www.ebi.ac.uk/efo/EFO_0004631, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90270936 Genome-wide genotyping array 2023-07-18 37384397 Scammell BH 2023-06-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37384397 Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration. Sleep duration 7,288 African ancestry individuals, 7,485 South Asian ancestry individuals, 8,726 Hispanic or Latin American individuals, 446,118 European ancestry individuals, 13,618 East Asian ancestry individuals NA NR [19794469] (imputed) 73 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90272876 Genome-wide genotyping array 2023-07-18 37384397 Scammell BH 2023-06-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37384397 Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration. Sleep duration 7,288 African ancestry individuals, 7,485 South Asian ancestry individuals, 8,726 Hispanic or Latin American individuals, 13,618 East Asian ancestry individuals NA NR [6014571] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90272877 Genome-wide genotyping array 2023-07-18 37384397 Scammell BH 2023-06-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37384397 Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration. Sleep duration 7,288 African ancestry individuals NA NR [9926106] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90272878 Genome-wide genotyping array 2023-07-18 37384397 Scammell BH 2023-06-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37384397 Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration. Sleep duration 7,485 South Asian ancestry individuals NA NR [9926106] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90272879 Genome-wide genotyping array 2023-07-18 37384397 Scammell BH 2023-06-29 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37384397 Multi-ancestry genome-wide analysis identifies shared genetic effects and common genetic variants for self-reported sleep duration. Sleep duration 8,726 Hispanic or Latin American individuals NA NR [11710371] (imputed) 0 sleep duration http://www.ebi.ac.uk/efo/EFO_0005271 GCST90272880 Genome-wide genotyping array 2023-07-21 37250466 Hatoum AS 2023-03-22 Nat Ment Health www.ncbi.nlm.nih.gov/pubmed/37250466 Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Addiction risk factors 300,789 European ancestry problematic alcohol use individuals, 270,120 European ancestry problematic tobacco use individuals, 46,351 European ancestry cannabis use disorder individuals, 30,443 European ancestry opioid use disorder individuals NA NR [3513381] (imputed) 19 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90274724 Genome-wide genotyping array 2023-07-21 37250466 Hatoum AS 2023-03-22 Nat Ment Health www.ncbi.nlm.nih.gov/pubmed/37250466 Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Substance use disorder (pleiotropy) 82,705 African American problematic alcohol use individuals, 9,925 African American problematic tobacco use individuals, 9,745 African American cannabis use disorder individuals, 32,088 African American opioid use disorder individuals NA NR [5303643] (imputed) 1 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90274725 Genome-wide genotyping array 2023-07-21 37250466 Hatoum AS 2023-03-22 Nat Ment Health www.ncbi.nlm.nih.gov/pubmed/37250466 Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Substance use disorder (pleiotropy) 300,789 European ancestry problematic alcohol use individuals, 270,120 European ancestry problematic tobacco use individuals, 46,351 European ancestry cannabis use disorder individuals, 30,443 European ancestry opioid use disorder individuals, 82,705 African American problematic alcohol use individuals, 9,925 African American problematic tobacco use individuals, 9,745 African American cannabis use disorder individuals, 32,088 African American opioid use disorder individuals NA NR [317447] (imputed) 20 substance-related disorder http://purl.obolibrary.org/obo/MONDO_0002494 GCST90274726 Genome-wide genotyping array 2023-07-21 37250466 Hatoum AS 2023-03-22 Nat Ment Health www.ncbi.nlm.nih.gov/pubmed/37250466 Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Problematic alcohol use 300,789 European ancestry individuals NA NR [NR] (imputed) 9 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90274727 Genome-wide genotyping array 2023-07-21 37250466 Hatoum AS 2023-03-22 Nat Ment Health www.ncbi.nlm.nih.gov/pubmed/37250466 Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Problematic tobacco use 270,120 European ancestry individuals NA NR [NR] (imputed) 32 nicotine dependence http://www.ebi.ac.uk/efo/EFO_0003768 GCST90274728 Genome-wide genotyping array 2023-07-21 37250466 Hatoum AS 2023-03-22 Nat Ment Health www.ncbi.nlm.nih.gov/pubmed/37250466 Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Cannabis use disorder 46,351 European ancestry individuals NA NR [NR] (imputed) 5 cannabis dependence http://www.ebi.ac.uk/efo/EFO_0007191 GCST90274729 Genome-wide genotyping array 2023-07-21 37250466 Hatoum AS 2023-03-22 Nat Ment Health www.ncbi.nlm.nih.gov/pubmed/37250466 Multivariate genome-wide association meta-analysis of over 1 million subjects identifies loci underlying multiple substance use disorders. Opioid use disorder 30,443 European ancestry individuals NA NR [NR] (imputed) 1 opioid use disorder http://www.ebi.ac.uk/efo/EFO_0010702 GCST90274730 Genome-wide genotyping array 2023-08-02 37012456 Sole-Navais P 2023-04-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37012456 Genetic effects on the timing of parturition and links to fetal birth weight. Preterm delivery 18,797 European ancestry cases, 260,246 European ancestry controls NA NR [NR] (imputed) 7 premature birth http://www.ebi.ac.uk/efo/EFO_0003917 GCST90275118 Genome-wide genotyping array 2023-08-02 37012456 Sole-Navais P 2023-04-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37012456 Genetic effects on the timing of parturition and links to fetal birth weight. Gestational duration 195,555 European ancestry individuals NA NR [NR] (imputed) 24 gestational age http://www.ebi.ac.uk/efo/EFO_0005112 GCST90275117 Genome-wide genotyping array 2023-08-02 37012456 Sole-Navais P 2023-04-03 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37012456 Genetic effects on the timing of parturition and links to fetal birth weight. Postterm delivery 15,972 European ancestry cases, 115,307 European ancestry controls NA NR [NR] (imputed) 1 post term pregnancy http://www.ebi.ac.uk/efo/EFO_0009681 GCST90275119 Genome-wide genotyping array 2023-07-28 37443256 Benonisdottir S 2023-07-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37443256 Studying the genetics of participation using footprints left on the ascertained genotypes. UK Biobank participation (transmitted–nontransmitted comparison) 4,427 European ancestry parent-offspring pairs NA NR [500632] 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90267220 Genome-wide genotyping array 2023-07-28 37443256 Benonisdottir S 2023-07-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37443256 Studying the genetics of participation using footprints left on the ascertained genotypes. UK Biobank participation (within-sib-pair comparison) 3,762 European ancestry sibling pairs (IBD=2 average sample size), 3,723 European ancestry sibling pairs (IBD=0 average sample size) NA NR [500632] 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90267221 Genome-wide genotyping array 2023-07-28 37443256 Benonisdottir S 2023-07-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37443256 Studying the genetics of participation using footprints left on the ascertained genotypes. UK Biobank participation (within-sib-pair comparison) 7,512 European ancestry sibling pairs (IBD=1 average sample size) NA NR [500632] 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90267222 Genome-wide genotyping array 2023-07-28 37443256 Benonisdottir S 2023-07-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37443256 Studying the genetics of participation using footprints left on the ascertained genotypes. UK Biobank participation (combined) 4,427 European ancestry parent-offspring pairs, 29,996 European ancestry sibling pairs (average sample size) NA NR [500632] 0 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90267223 Genome-wide genotyping array 2023-07-13 36981009 Zou T 2023-03-17 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/36981009 Genome-Wide Analysis of Dental Caries Variability Reveals Genotype-by-Environment Interactions. Primary dental caries (decayed and filled teeth) 1,497 European ancestry children NA Illumina [4300000] (imputed) 5 primary dental caries http://www.ebi.ac.uk/efo/EFO_0600095 GCST90271954 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-2,3-dinor-TXB2 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296207 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-2,3-dinor-TXB2 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296208 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296209 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296210 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGE2, Eicosanoid 15k PGF2a, Eicosanoid PGD2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296211 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11d-TXB2 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296212 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11d-TXB2 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296213 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11t LTD4 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 3 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296214 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpEPE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296215 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296216 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296217 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296218 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME, Eicosanoid 9,10 diHOME a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296219 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME, Eicosanoid 9,10 diHOME b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296220 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296221 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296222 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HHTrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296223 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296224 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296225 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296226 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA d levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296227 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HEPE, Eicosanoid 15S-HEPE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296228 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-oxoETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296229 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-oxoETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296230 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13S-HpOTrE(gamma) levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296231 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 19,20-EpDPA, Eicosanoid 11 HDoHE, Eicosanoid 7 HDoHE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296107 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7,8-DiHDPA levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296108 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7-epi-Maresin 1 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296109 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7-epi-Maresin 1 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296110 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid MCTR2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296111 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 1 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296112 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 1 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296113 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296114 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296115 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296116 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D2, Docosanoid Resolvin D3 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296117 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D2, Docosanoid Resolvin D3 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296118 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D4 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296119 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin E1, Eicosanoid 19R-hydroxy-PGA2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296120 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid osbond acid, all-cis-4,7,10,13,16-DPA, FFA Docosapentaenoic Acid levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 4 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296121 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-HETE, Eicosanoid 12-HETE, Eicosanoid 8-HETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296122 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296123 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE e levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296124 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE d levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296125 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296126 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-HETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296127 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296128 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296129 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17-HETE, Eicosanoid 18(+/-)-HETE, Eicosanoid 20-HETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 3 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296130 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 19(R)-HETE, Eicosanoid 20-HETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296131 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HEPE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296182 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17(18) EpETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296183 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGD2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296184 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296185 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296186 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13S-HpOTrE, Eicosanoid 9S-HpOTrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296187 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9S-HpOTrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296188 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296189 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296190 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296191 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296192 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17(18) EpETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296193 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296194 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HEPE, Eicosanoid 9(S) HEPE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296195 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12(S) HEPE, Eicosanoid 15(S) HEPE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296196 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296197 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-HETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296198 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 10-Nitrooleate, Eicosanoid 9-Nitrooleate levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296199 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-EET, Eicosanoid 8,9-EET a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296200 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-EET, Eicosanoid 8,9-EET b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296201 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11(12)-EpETE, Eicosanoid 14(15) EpETE, Eicosanoid 15-oxoETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296202 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11(12)-EpETE, Eicosanoid 14(15) EpETE, Eicosanoid 15-oxoETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296203 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-diHETrE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296204 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-diHETrE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296205 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-HETE, Eicosanoid 12-HETE, Eicosanoid 8-HETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296206 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15(S) HETrE, Eicosanoid 8(S) HETrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296132 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HETrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296133 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296134 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296135 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296136 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296137 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296138 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGJ2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296139 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296140 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296141 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17,18-DiHETE, Eicosanoid 5,12-DiHETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296142 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296143 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12epi LTB4, Eicosanoid 14,15-DiHETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296144 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296145 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 3 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296146 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296147 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296148 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 d levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296149 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296150 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296151 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296152 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296153 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296154 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-diHETrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296155 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17k DPA, Eicosanoid 8 HDoHE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296156 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 14S-HDHA, Docosanoid 17R-HDHA levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296157 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid LXA5 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296158 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGD3, Eicosanoid PGE3 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296159 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296160 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-HODE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296161 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HODE, Eicosanoid 9-HODE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296162 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296163 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296164 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b dhk PGF2a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296165 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGF2a, Eicosanoid 5-iso PGF2a a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296166 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGF2a, Eicosanoid 5-iso PGF2a b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296167 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE1, Eicosanoid 15R-PGF2alp a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296168 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE1, Eicosanoid 15R-PGF2alp b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296169 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15k PGF1a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296170 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296171 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296172 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296173 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 EpOME, Eicosanoid 9,10 EpOME levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296174 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 7,17 dhDPA a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296175 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 7,17 dhDPA b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296176 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 13,14-DiHDPA, Docosanoid 16,17-DiHDPA levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296177 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 16,17-DiHDPA, Docosanoid 19,20-DiHDPA levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296178 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296179 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid TXB3 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296180 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 6k PGE1, Eicosanoid 6-keto PGE1 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296181 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Dihydroxydocosapentaenoic acid levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274652 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274653 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274654 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid d levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274655 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3, Eicosanoid HXB3 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274656 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3, Eicosanoid HXB3 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274657 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid LXA5, Eicosanoid PGD3 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274658 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PDX, Eicosanoid Resolvin D5 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274659 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGA3 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274660 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGD3, Eicosanoid PGE3 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274661 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGE3 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274662 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274663 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274664 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274665 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF3a a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274666 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF3a b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274667 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid Resolvin D1 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274668 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274669 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274670 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274671 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274672 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 10,11-DiHDPA levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296103 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 10,11-EpDPA, Docosanoid 13,14-EpDPA levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296104 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 17S-HpDHA a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296105 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 17S-HpDHA c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296106 Genome-wide genotyping array 2023-11-06 37165155 Leonardsen EH 2023-05-10 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/37165155 Genetic architecture of brain age and its causal relations with brain and mental disorders. Brain age gap 28,104 individuals NA NR [8600000] (imputed) 8 brain age measurement http://www.ebi.ac.uk/efo/EFO_0010602 GCST90296682 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Plasma protein N-glycan peak 29 levels in type 1 diabetes 1,074 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 N-glycan measurement http://www.ebi.ac.uk/efo/EFO_0004999 GCST90271818 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Plasma protein N-glycan peak 6 levels in type 1 diabetes 1,074 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 N-glycan measurement http://www.ebi.ac.uk/efo/EFO_0004999 GCST90271819 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Plasma protein N-glycan peak 19 levels in type 1 diabetes 1,074 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 0 N-glycan measurement http://www.ebi.ac.uk/efo/EFO_0004999 GCST90271820 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 10 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 2 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271821 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 11 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271822 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 15 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271823 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 16 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271824 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 19 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271825 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 23 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271826 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 24 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271827 Genome-wide genotyping array 2023-07-12 36907892 Rudman N 2023-03-13 Diabetologia www.ncbi.nlm.nih.gov/pubmed/36907892 Integrated glycomics and genetics analyses reveal a potential role for N-glycosylation of plasma proteins and IgGs, as well as the complement system, in the development of type 1 diabetes. Immunoglobulin G N-glycan peak 6 levels in type 1 diabetes 1,086 child cases 190 child cases, 265 unaffected sibling controls Illumina [108428] 1 serum IgG glycosylation measurement http://www.ebi.ac.uk/efo/EFO_0005193 GCST90271828 Genome-wide genotyping array 2023-11-15 37208024 Bradley J 2023-05-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37208024 Genetic architecture of plasma Alzheimer disease biomarkers. Plasma amyloid beta 40 levels 1,964 European ancestry individuals NA Illumina [13791029] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90297539 Genome-wide genotyping array 2023-11-15 37208024 Bradley J 2023-05-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37208024 Genetic architecture of plasma Alzheimer disease biomarkers. Plasma amyloid beta 42 levels 1,985 European ancestry individuals NA Illumina [13791029] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90297540 Genome-wide genotyping array 2023-11-15 37208024 Bradley J 2023-05-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37208024 Genetic architecture of plasma Alzheimer disease biomarkers. Plasma amyloid beta 42 to 40 ratio 1,991 European ancestry individuals NA Illumina [13791029] (imputed) 1 amyloid-beta measurement http://www.ebi.ac.uk/efo/EFO_0005194 GCST90297541 Genome-wide genotyping array 2023-11-15 37208024 Bradley J 2023-05-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37208024 Genetic architecture of plasma Alzheimer disease biomarkers. Plasma neurofilament light levels 2,380 European ancestry individuals NA Illumina [13791029] (imputed) 5 neurofilament light chain measurement http://www.ebi.ac.uk/efo/EFO_0009178 GCST90297542 Genome-wide genotyping array 2023-11-15 37208024 Bradley J 2023-05-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37208024 Genetic architecture of plasma Alzheimer disease biomarkers. Plasma t-tau levels 563 European ancestry individuals NA Illumina [13791029] (imputed) 2 t-tau measurement http://www.ebi.ac.uk/efo/EFO_0004760 GCST90297543 Genome-wide genotyping array 2023-11-15 37208024 Bradley J 2023-05-19 Hum Mol Genet www.ncbi.nlm.nih.gov/pubmed/37208024 Genetic architecture of plasma Alzheimer disease biomarkers. Plasma p-tau181 levels 1,186 European ancestry individuals NA Illumina [13791029] (imputed) 3 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90297544 Genome-wide genotyping array 2023-07-11 36893272 Makowski C 2023-03-09 Proc Natl Acad Sci U S A www.ncbi.nlm.nih.gov/pubmed/36893272 Larger cerebral cortex is genetically correlated with greater frontal area and dorsal thickness. Cortical thickness 32,488 European ancestry individuals 3,776 children, 5,360 European ancestry children NR [7598201] (imputed) 19 cortical thickness http://www.ebi.ac.uk/efo/EFO_0004840 GCST90271815 Genome-wide genotyping array 2023-07-13 36931692 Styrkarsdottir U 2023-03-17 Ann Rheum Dis www.ncbi.nlm.nih.gov/pubmed/36931692 Meta-analysis of erosive hand osteoarthritis identifies four common variants that associate with relatively large effect. Erosive hand osteoarthritis 1,484 European ancestry cases, 550,680 European ancestry controls NA Affymetrix, Illumina [1200000] (imputed) 4 osteoarthritis, hand http://www.ebi.ac.uk/efo/EFO_1000789 GCST90271957 Genome-wide genotyping array 2023-08-16 37062025 He YQ 2023-04-16 Hum Genet www.ncbi.nlm.nih.gov/pubmed/37062025 Clinical and genome-wide association analysis of chemoradiation-induced hearing loss in nasopharyngeal carcinoma. Chemoradiation-induced hearing loss in nasopharyngeal carcinoma 132 East Asian ancestry cases, 645 East Asian ancestry controls NA Illumina [5248879] (imputed) 30 response to radiation, hearing loss, response to antineoplastic agent http://purl.obolibrary.org/obo/GO_0009314, http://www.ebi.ac.uk/efo/EFO_0004238, http://purl.obolibrary.org/obo/GO_0097327 GCST90277553 Genome-wide genotyping array 2023-06-27 36806387 Bandesh K 2023-02-17 Int J Obes (Lond) www.ncbi.nlm.nih.gov/pubmed/36806387 Identification and characterization of the long non-coding RNA NFIA-AS2 as a novel locus for body mass index in American Indians. Body mass index 5,870 Native American ancestry individuals 240,608 individuals Affymetrix [5077595] (imputed) 12 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90271560 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. MUC5B concentration x pack-years of smoking interaction (2df) 215 European ancestry individuals NA NR [8308642] (imputed) 0 pack-years measurement, sputum mucin-5B amount http://www.ebi.ac.uk/efo/EFO_0006526, http://purl.obolibrary.org/obo/OBA_2050332 GCST90269929 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. MUC5AC concentration 215 European ancestry individuals NA NR [8308642] (imputed) 2 sputum mucin-5AC amount http://purl.obolibrary.org/obo/OBA_2050331 GCST90269930 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. Sputum mucin protein concentration 132 African American or Afro-Caribbean individuals, 576 European ancestry individuals NA NR [9794161] (imputed) 0 sputum mucin measurement http://www.ebi.ac.uk/efo/EFO_0803538 GCST90269925 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. Sputum mucin protein concentration x pack-years of smoking interaction (2df) 576 European ancestry individuals NA NR [9794161] (imputed) 0 pack-years measurement, sputum mucin measurement http://www.ebi.ac.uk/efo/EFO_0006526, http://www.ebi.ac.uk/efo/EFO_0803538 GCST90269926 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. Sputum mucin protein concentration 576 European ancestry individuals NA NR [9794161] (imputed) 0 sputum mucin measurement http://www.ebi.ac.uk/efo/EFO_0803538 GCST90269927 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. Sputum mucin protein concentration x pack-years of smoking interaction (2df) 132 African American or Afro-Caribbean individuals NA NR [11201942] (imputed) 0 pack-years measurement, sputum mucin measurement http://www.ebi.ac.uk/efo/EFO_0006526, http://www.ebi.ac.uk/efo/EFO_0803538 GCST90269923 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. Sputum mucin protein concentration 132 African American or Afro-Caribbean individuals NA NR [11201942] (imputed) 0 sputum mucin measurement http://www.ebi.ac.uk/efo/EFO_0803538 GCST90269924 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. MUC5AC concentration x pack-years of smoking interaction (2df) 215 European ancestry individuals NA NR [8308642] (imputed) 0 pack-years measurement, sputum mucin-5AC amount http://www.ebi.ac.uk/efo/EFO_0006526, http://purl.obolibrary.org/obo/OBA_2050331 GCST90269928 Genome-wide genotyping array 2023-08-30 37352370 Buren EV 2023-06-23 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/37352370 Genetic regulators of sputum mucin concentration and their associations with COPD phenotypes. MUC5B concentration 215 European ancestry individuals NA NR [8308642] (imputed) 2 sputum mucin-5B amount http://purl.obolibrary.org/obo/OBA_2050332 GCST90269931 Genome-wide genotyping array 2023-08-02 37049604 Park S 2023-04-04 Nutrients www.ncbi.nlm.nih.gov/pubmed/37049604 Height-Related Polygenic Variants Are Associated with Metabolic Syndrome Risk and Interact with Energy Intake and a Rice-Main Diet to Influence Height in KoGES. Height 58,701 Korean ancestry individuals 13,783 Korean ancestry individuals Affymetrix [NR] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90275120 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (default mode network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271728 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (dorsal attention network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271729 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (frontoparietal network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271730 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (limbic network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271731 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (somatomotor network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271732 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (ventral attention network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271733 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (visual network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271734 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Functional connectivity (global network) 24,336 European ancestry individuals 3,408 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271735 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (default mode network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271736 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (dorsal attention network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271737 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (frontoparietal network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271738 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (limbic network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271739 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (somatomotor network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271740 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (ventral attention network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271741 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (visual network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271742 Genome-wide genotyping array 2023-07-07 36882310 Tissink E 2023-03-06 eNeuro www.ncbi.nlm.nih.gov/pubmed/36882310 The genetic architectures of functional and structural connectivity properties within cerebral resting-state networks. Structural connectivity (global network) 23,985 European ancestry individuals 3,412 European ancestry individuals Affymetrix [9380668] (imputed) 0 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90271743 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274278 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-diHETrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274279 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17k DPA, Eicosanoid 8 HDoHE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274280 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 14S-HDHA, Docosanoid 17R-HDHA levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274281 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid LXA5 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274282 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGD3, Eicosanoid PGE3 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274283 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274284 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-HODE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274285 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HODE, Eicosanoid 9-HODE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274286 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274287 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274288 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b dhk PGF2a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274289 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGF2a, Eicosanoid 5-iso PGF2a a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274290 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGF2a, Eicosanoid 5-iso PGF2a b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274291 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE1, Eicosanoid 15R-PGF2alp a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274292 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE1, Eicosanoid 15R-PGF2alp b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274293 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15k PGF1a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274294 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274295 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274296 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274297 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 EpOME, Eicosanoid 9,10 EpOME levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274298 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 7,17 dhDPA a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274299 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 7,17 dhDPA b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274300 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 13,14-DiHDPA, Docosanoid 16,17-DiHDPA levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274301 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 16,17-DiHDPA, Docosanoid 19,20-DiHDPA levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274302 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 10,11-EpDPA, Docosanoid 13,14-EpDPA levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274228 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 17S-HpDHA a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274229 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 17S-HpDHA c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274230 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 19,20-EpDPA, Eicosanoid 11 HDoHE, Eicosanoid 7 HDoHE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274231 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7,8-DiHDPA levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274232 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7-epi-Maresin 1 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274233 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7-epi-Maresin 1 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274234 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid MCTR2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274235 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 1 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274236 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 1 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274237 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274238 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274239 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274240 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D2, Docosanoid Resolvin D3 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274241 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D2, Docosanoid Resolvin D3 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274242 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D4 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274243 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin E1, Eicosanoid 19R-hydroxy-PGA2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274244 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid osbond acid, all-cis-4,7,10,13,16-DPA, FFA Docosapentaenoic Acid levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274245 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-HETE, Eicosanoid 12-HETE, Eicosanoid 8-HETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274246 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274247 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE e levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274248 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE d levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274249 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274250 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-HETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274251 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274252 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HEPE, Eicosanoid 15S-HEPE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274352 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-oxoETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274353 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-oxoETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274354 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13S-HpOTrE(gamma) levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274355 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274356 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-tetranor-PGD2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274357 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-tetranor-PGF1alpha levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274358 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGE1 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274359 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGE1 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274360 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGF1a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274361 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274362 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE, Eicosanoid 9-HpODE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274363 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE, Eicosanoid 9-HpODE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274364 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274365 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274366 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274367 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE(y) levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274368 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274369 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274370 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET, Eicosanoid 5-HETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274371 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. 11-hydroxy-9-octadecenoate, 10-hydroxy-11-octadecenoate levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274372 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET, Eicosanoid 5-HETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274373 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4, Eicosanoid PGA2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274374 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-diHETrE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274375 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274376 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274427 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Docosahexaenoic Acid levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274428 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Dihydroxydocosapentaenoic acid levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274429 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274430 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274431 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid d levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274432 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3, Eicosanoid HXB3 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274433 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3, Eicosanoid HXB3 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274434 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid LXA5, Eicosanoid PGD3 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274435 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PDX, Eicosanoid Resolvin D5 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274436 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGA3 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274437 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGD3, Eicosanoid PGE3 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274438 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGE3 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274439 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274440 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274441 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274442 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF3a a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274443 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF3a b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274444 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid Resolvin D1 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274445 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274446 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274447 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274448 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274449 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 10,11-DiHDPA levels 6,496 European ancestry individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274450 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 10,11-EpDPA, Docosanoid 13,14-EpDPA levels 6,496 European ancestry individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274451 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274253 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17-HETE, Eicosanoid 18(+/-)-HETE, Eicosanoid 20-HETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274254 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 19(R)-HETE, Eicosanoid 20-HETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274255 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15(S) HETrE, Eicosanoid 8(S) HETrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274256 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HETrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274257 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274258 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274259 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274260 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274261 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274262 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGJ2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274263 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274264 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274265 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17,18-DiHETE, Eicosanoid 5,12-DiHETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274266 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274267 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12epi LTB4, Eicosanoid 14,15-DiHETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274268 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274269 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274270 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274271 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274272 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 d levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274273 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274274 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274275 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274276 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274277 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274377 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274378 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15S-HpETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274379 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274380 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274381 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15 oxoEDE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274382 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15 oxoEDE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274383 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-oxoETE, Eicosanoid 17(18) EpETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274384 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGA2 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274385 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGA2 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274386 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGJ2 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274387 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGJ2 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274388 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15t-Protectin D1 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274389 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274390 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17S-HpDHA d levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274391 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17S-HpDHA b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274392 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274393 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274394 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274395 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3-dinor-PGE1 a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274396 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3-dinor-PGE1 b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274397 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3 dinor TXB2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274398 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpEPE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274399 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274400 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274401 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274303 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid TXB3 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274304 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 6k PGE1, Eicosanoid 6-keto PGE1 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274305 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HEPE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274306 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17(18) EpETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274307 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGD2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274308 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274309 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274310 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13S-HpOTrE, Eicosanoid 9S-HpOTrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274311 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9S-HpOTrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274312 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274313 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274314 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274315 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274316 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17(18) EpETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274317 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274318 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME, Eicosanoid 9,10 diHOME a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274343 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME, Eicosanoid 9,10 diHOME b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274344 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274345 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274346 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HHTrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274347 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274348 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274349 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274350 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA d levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274351 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274402 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-EET levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274403 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274404 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274405 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274406 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274407 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274408 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274409 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274410 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274411 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE c levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274412 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HETrE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274413 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-15k PGF2b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274414 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1 levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274415 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGF1a, Eicosanoid 8-iso-PGF1b, Eicosanoid PGF1beta a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274416 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 EpOME a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274417 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 EpOME b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274418 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 diHOME levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274419 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9(S) HOTrE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274420 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274421 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274422 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Adrenic Acid a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274423 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Adrenic Acid b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274424 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid a levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274425 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid b levels 1,910 African American individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274426 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296282 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296283 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296284 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296285 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 3 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296286 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296287 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296288 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HETrE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296289 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-15k PGF2b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296290 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296291 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGF1a, Eicosanoid 8-iso-PGF1b, Eicosanoid PGF1beta a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296292 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 EpOME a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296293 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 EpOME b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296294 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 diHOME levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296295 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9(S) HOTrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296296 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296297 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296298 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Adrenic Acid a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 4 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296299 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Adrenic Acid b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296300 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296301 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296302 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296303 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Docosahexaenoic Acid levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296304 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Dihydroxydocosapentaenoic acid levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296305 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296306 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296232 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-tetranor-PGD2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296233 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-tetranor-PGF1alpha levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296234 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGE1 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296235 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGE1 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296236 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGF1a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296237 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 4 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296238 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE, Eicosanoid 9-HpODE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296239 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE, Eicosanoid 9-HpODE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296240 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296241 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296242 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296243 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE(y) levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296244 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296245 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296246 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET, Eicosanoid 5-HETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296247 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. 11-hydroxy-9-octadecenoate, 10-hydroxy-11-octadecenoate levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296248 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET, Eicosanoid 5-HETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296249 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4, Eicosanoid PGA2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296250 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-diHETrE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296251 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296252 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296253 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296254 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15S-HpETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296255 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296256 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296257 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15 oxoEDE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296258 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15 oxoEDE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296259 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-oxoETE, Eicosanoid 17(18) EpETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296260 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGA2 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296261 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGA2 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296262 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGJ2 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296263 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGJ2 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296264 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15t-Protectin D1 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296265 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296266 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17S-HpDHA d levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296267 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17S-HpDHA b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296268 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296269 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296270 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 3 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296271 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3-dinor-PGE1 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296272 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3-dinor-PGE1 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296273 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3 dinor TXB2 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296274 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpEPE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 3 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296275 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296276 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296277 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296278 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-EET levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296279 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296280 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296281 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 3 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296307 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Eicosapentaenoic Acid d levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296308 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3, Eicosanoid HXB3 a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296309 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3, Eicosanoid HXB3 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296310 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid LXA5, Eicosanoid PGD3 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296311 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PDX, Eicosanoid Resolvin D5 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296312 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGA3 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296313 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGD3, Eicosanoid PGE3 b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296314 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGE3 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296315 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296316 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296317 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF1a c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296318 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF3a a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296319 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGF3a b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296320 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid Resolvin D1 levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296321 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 1 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296322 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE a levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296323 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE b levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 2 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296324 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid tetranor 12(R) HETE c levels 1,910 African American individuals, 6,496 European ancestry individuals NA Affymetrix [Affymetrix 6.0 DNA microarray] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90296325 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. AGRP levels 961 individuals NA Illumina [11901634] (imputed) 16 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST009696 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CCL19 levels 953 individuals NA Illumina [11901634] (imputed) 3 CCL19 measurement http://www.ebi.ac.uk/efo/EFO_0009415 GCST90274880 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CCL24 levels 953 individuals NA Illumina [11901634] (imputed) 23 CCL24 measurement http://www.ebi.ac.uk/efo/EFO_0009418 GCST90274881 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CCL4 levels 961 individuals NA Illumina [11901634] (imputed) 8 CCL4 measurement http://www.ebi.ac.uk/efo/EFO_0004751 GCST90274882 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CD30-L levels 319 individuals NA Illumina [11901634] (imputed) 1 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90274883 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CD40 levels 961 individuals NA Illumina [11901634] (imputed) 1 CD40 measurement http://www.ebi.ac.uk/efo/EFO_0010586 GCST90274884 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CHI3L1 levels 959 individuals NA Illumina [11901634] (imputed) 1 YKL40 measurement http://www.ebi.ac.uk/efo/EFO_0004869 GCST90274885 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CXCL10 levels 953 individuals NA Illumina [11901634] (imputed) 51 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST90274886 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CXCL5 levels 953 individuals NA Illumina [11901634] (imputed) 4 C-X-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008058 GCST90274887 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. CXCL6 levels 961 individuals NA Illumina [11901634] (imputed) 1 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90274888 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. Cystatin B levels 949 individuals NA Illumina [11901634] (imputed) 1 cystatin B measurement http://www.ebi.ac.uk/efo/EFO_0010593 GCST90274889 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. E-selectin levels 953 individuals NA Illumina [11901634] (imputed) 2 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90274890 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. Ep-CAM levels 953 individuals NA Illumina [11901634] (imputed) 60 epithelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010574 GCST90274891 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. Flt3L levels 953 individuals NA Illumina [11901634] (imputed) 4 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90274892 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. Galectin-3 levels 953 individuals NA Illumina [11901634] (imputed) 1 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90274893 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. HSP_27 levels 919 individuals NA Illumina [11901634] (imputed) 1 heat shock protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0010595 GCST90274894 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. IL-12 levels 953 individuals NA Illumina [11901634] (imputed) 1 interleukin 12 measurement http://www.ebi.ac.uk/efo/EFO_0004753 GCST90274895 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. IL17RB levels 609 individuals NA Illumina [11901634] (imputed) 2 interleukin 17 receptor B measurement http://www.ebi.ac.uk/efo/EFO_0008176 GCST90274896 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. IL2RA levels 953 individuals NA Illumina [11901634] (imputed) 10 interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0010587 GCST90274897 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. IL6RA levels 953 individuals NA Illumina [11901634] (imputed) 6 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90274898 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. kallikrein-11 levels 943 individuals NA Illumina [11901634] (imputed) 1 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90274899 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MCP-1 levels 953 individuals NA Illumina [11901634] (imputed) 1 monocyte chemotactic protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010596 GCST90274900 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MIA levels 949 individuals NA Illumina [11901634] (imputed) 1 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90274901 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MIC-A levels 530 individuals NA Illumina [11901634] (imputed) 15 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST90274902 Genome-wide genotyping array 2023-07-28 28915241 Ahsan M 2017-09-15 PLoS Genet www.ncbi.nlm.nih.gov/pubmed/28915241 The relative contribution of DNA methylation and genetic variants on protein biomarkers for human diseases. MMP-1 levels 931 individuals NA Illumina [11901634] (imputed) 1 matrix metalloproteinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0010588 GCST90274903 Genome-wide genotyping array 2023-07-12 36963307 Nudel R 2023-03-16 Psychiatry Res www.ncbi.nlm.nih.gov/pubmed/36963307 Developmental language disorder - a comprehensive study of more than 46,000 individuals. Developmental language disorder 610 European ancestry cases, 17,770 European ancestry controls NA Illumina [162466] (imputed) 1 specific language impairment http://www.ebi.ac.uk/efo/EFO_1001510 GCST90271931 Genome-wide genotyping array 2023-11-10 37895268 Alshabeeb MA 2023-10-09 Genes (Basel) www.ncbi.nlm.nih.gov/pubmed/37895268 Impact of Genetic Variations on Thromboembolic Risk in Saudis with Sickle Cell Disease. Thromboembolic events in Sickle cell disease 65 Saudis ancestry cases, 285 Saudis ancestry controls NA Affymetrix [NR] 31 Thromboembolism http://purl.obolibrary.org/obo/HP_0001907 GCST90296723 Genome-wide genotyping array 2023-07-12 37357295 Axelsen TM 2023-01-01 J Prev Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/37357295 A Genetic Validation of the Neurodegeneration Biomarkers Tau-A and Tau-C - A Mendelian Randomization Study. Serum Tau-A levels 4,968 Danish ancestry individuals NA Illumina [7000000] (imputed) 1 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90271816 Genome-wide genotyping array 2023-07-12 37357295 Axelsen TM 2023-01-01 J Prev Alzheimers Dis www.ncbi.nlm.nih.gov/pubmed/37357295 A Genetic Validation of the Neurodegeneration Biomarkers Tau-A and Tau-C - A Mendelian Randomization Study. Serum Tau-C levels 4,968 Danish ancestry individuals NA Illumina [7000000] (imputed) 1 p-tau measurement http://www.ebi.ac.uk/efo/EFO_0004763 GCST90271817 Genome-wide genotyping array 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 1 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90271642 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 18 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90271643 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. 3-aminoisobutyrate levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 3 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90271644 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Arachidonate (20:4n6) levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 18 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90271645 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Choline levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 15 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90271646 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Gamma-glutamyl-2-aminobutyrate levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 6 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90271647 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Glycerophosphoethanolamine levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 3 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90271648 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Leucylglycine levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 6 leucylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800678 GCST90271649 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Metabolonic lactone sulfate levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 7 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90271650 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Methyl glucopyranoside (alpha + beta) levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 1 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90271651 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N-palmitoyl-sphinganine (d18:0/16:0) levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 1 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90271652 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N2-acetyl,N6,N6-dimethyllysine levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 9 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90271653 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N6,N6-dimethyllysine levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 9 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90271654 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N6-methyllysine levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 9 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90271655 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. succinylcarnitine measurement (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 8 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90271656 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Valylglycine levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 9 valylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800680 GCST90271657 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Valylleucine levels (advanced age) 116 Han Chinese ancestry individuals NA NR [114055] 8 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90271658 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 1 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90271659 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 18 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90271660 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. 3-aminoisobutyrate levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 3 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90271661 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Arachidonate (20:4n6) levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 18 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90271662 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Choline levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 15 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90271663 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Gamma-glutamyl-2-aminobutyrate levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 6 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90271664 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Glycerophosphoethanolamine levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 3 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90271665 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Leucylglycine levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 6 leucylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800678 GCST90271666 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Metabolonic lactone sulfate levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 7 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90271667 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Methyl glucopyranoside (alpha + beta) levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 1 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90271668 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N-palmitoyl-sphinganine (d18:0/16:0) levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 1 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90271669 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N2-acetyl,N6,N6-dimethyllysine levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 9 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90271670 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N6,N6-dimethyllysine levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 9 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90271671 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. N6-methyllysine levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 9 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90271672 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. succinylcarnitine measurement (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 8 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90271673 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Valylglycine levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 9 valylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800680 GCST90271674 Exome-wide sequencing 2023-06-30 37118062 Xu Q 2022-04-14 Nat Aging www.ncbi.nlm.nih.gov/pubmed/37118062 Metagenomic and metabolomic remodeling in nonagenarians and centenarians and its association with genetic and socioeconomic factors. Valylleucine levels (elderly offspring) 232 Han Chinese ancestry individuals NA NR [111420] 8 peptide measurement http://www.ebi.ac.uk/efo/EFO_0010520 GCST90271675 Exome-wide sequencing 2023-06-22 37089865 Pu A 2023-02-08 Front Drug Discov (Lausanne) www.ncbi.nlm.nih.gov/pubmed/37089865 Identification of novel genetic variants, including PIM1 and LINC01491, with ICD-10 based diagnosis of pulmonary arterial hypertension in the UK Biobank cohort. ICD10 127.0 pulmonary arterial hypertension 493 British ancestry cases, 24,650 British ancestry controls NA NR [40000000] (imputed) 9 pulmonary arterial hypertension http://www.ebi.ac.uk/efo/EFO_0001361 GCST90270938 Genome-wide genotyping array 2023-07-11 37386106 Mignogna G 2023-06-29 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37386106 Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci. Non-response to survey questionnaires: "I don't know" item 360,628 European ancestry individuals NA Affymetrix [9367367] (imputed) 37 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90266935 Genome-wide genotyping array 2023-07-11 37386106 Mignogna G 2023-06-29 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37386106 Patterns of item nonresponse behaviour to survey questionnaires are systematic and associated with genetic loci. Non-response to survey questionnaires: "prefer not to answer" item 360,628 European ancestry individuals NA Affymetrix [9367367] (imputed) 4 health study participation http://www.ebi.ac.uk/efo/EFO_0010130 GCST90266936 Genome-wide genotyping array 2023-07-03 36246171 Fuse N 2022-01-22 Ophthalmol Sci www.ncbi.nlm.nih.gov/pubmed/36246171 Genome-wide Association Study of Axial Length in Population-based Cohorts in Japan: The Tohoku Medical Megabank Organization Eye Study. Axial length 33,483 Japanese ancestry individuals NA Affymetrix [8585409] (imputed) 31 axial length measurement http://www.ebi.ac.uk/efo/EFO_0005318 GCST90239583 Genome-wide genotyping array 2023-07-12 37365406 Hindley G 2023-06-26 Nat Hum Behav www.ncbi.nlm.nih.gov/pubmed/37365406 Multivariate genetic analysis of personality and cognitive traits reveals abundant pleiotropy. Personality traits or cognitive traits (multivariate analysis) 337,125 British ancestry individuals NA NR [12926669] (imputed) 431 neuroticism measurement, cognitive function measurement http://www.ebi.ac.uk/efo/EFO_0007660, http://www.ebi.ac.uk/efo/EFO_0008354 GCST90270074 Genome-wide genotyping array 2023-07-24 36864640 Zhang L 2023-03-02 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/36864640 A brain-wide genome-wide association study of candidate quantitative trait loci associated with structural and functional phenotypes of pain sensitivity. Right insula grey matter density 407 individuals NA Affymetrix [353421] 1 Grey matter density measurement http://www.ebi.ac.uk/efo/EFO_0010306 GCST90274224 Genome-wide genotyping array 2023-07-24 36864640 Zhang L 2023-03-02 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/36864640 A brain-wide genome-wide association study of candidate quantitative trait loci associated with structural and functional phenotypes of pain sensitivity. Resting state functional connectivity between right insula and left putamen 390 individuals NA Affymetrix [353421] 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90274225 Genome-wide genotyping array 2023-07-24 36864640 Zhang L 2023-03-02 Cereb Cortex www.ncbi.nlm.nih.gov/pubmed/36864640 A brain-wide genome-wide association study of candidate quantitative trait loci associated with structural and functional phenotypes of pain sensitivity. Resting state functional connectivity between dorsal anterior insula and left putamen 390 individuals NA Affymetrix [353421] 1 brain connectivity measurement http://www.ebi.ac.uk/efo/EFO_0005210 GCST90274226 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-oxoETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274577 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13S-HpOTrE(gamma) levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274578 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274579 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-tetranor-PGD2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274580 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-tetranor-PGF1alpha levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274581 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGE1 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274582 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGE1 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274583 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-PGF1a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274584 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274585 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE, Eicosanoid 9-HpODE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274586 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HpODE, Eicosanoid 9-HpODE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274587 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274588 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274589 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE, Eicosanoid 9(S) HOTrE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274590 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13(S) HOTrE(y) levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274591 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274592 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274593 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET, Eicosanoid 5-HETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274594 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. 11-hydroxy-9-octadecenoate, 10-hydroxy-11-octadecenoate levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274595 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET, Eicosanoid 5-HETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274596 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4, Eicosanoid PGA2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274597 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-diHETrE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274598 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274599 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274600 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274601 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-diHETrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274502 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17k DPA, Eicosanoid 8 HDoHE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274503 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 14S-HDHA, Docosanoid 17R-HDHA levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274504 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid LXA5 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274505 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid PGD3, Eicosanoid PGE3 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274506 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274507 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-HODE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274508 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-HODE, Eicosanoid 9-HODE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274509 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-LXA4, Eicosanoid 6R-LXA4 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274510 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE2, Eicosanoid 8-iso-15-keto-PGF2alpha a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274511 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b dhk PGF2a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274512 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGF2a, Eicosanoid 5-iso PGF2a a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274513 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGF2a, Eicosanoid 5-iso PGF2a b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274514 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE1, Eicosanoid 15R-PGF2alp a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274515 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15R-PGE1, Eicosanoid 15R-PGF2alp b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274516 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15k PGF1a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274517 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274518 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274519 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGD1 c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274520 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 EpOME, Eicosanoid 9,10 EpOME levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274521 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 7,17 dhDPA a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274522 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 7,17 dhDPA b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274523 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 13,14-DiHDPA, Docosanoid 16,17-DiHDPA levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274524 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 16,17-DiHDPA, Docosanoid 19,20-DiHDPA levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274525 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274526 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 17S-HpDHA a levels 6,496 European ancestry individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274452 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 17S-HpDHA c levels 6,496 European ancestry individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274453 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 19,20-EpDPA, Eicosanoid 11 HDoHE, Eicosanoid 7 HDoHE levels 6,496 European ancestry individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274454 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7,8-DiHDPA levels 6,496 European ancestry individuals NA Affymetrix [14854802] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274455 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7-epi-Maresin 1 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274456 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid 7-epi-Maresin 1 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274457 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid MCTR2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274458 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 1 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274459 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 1 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274460 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274461 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274462 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Maresin 2 c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274463 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D2, Docosanoid Resolvin D3 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274464 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D2, Docosanoid Resolvin D3 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274465 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin D4 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274466 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid Resolvin E1, Eicosanoid 19R-hydroxy-PGA2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274467 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Docosanoid osbond acid, all-cis-4,7,10,13,16-DPA, FFA Docosapentaenoic Acid levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274468 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-HETE, Eicosanoid 12-HETE, Eicosanoid 8-HETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274469 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274470 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE e levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274471 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE d levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274472 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-EET b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274473 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-HETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274474 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274475 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274476 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid TXB3 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274527 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 6k PGE1, Eicosanoid 6-keto PGE1 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274528 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HEPE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274529 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17(18) EpETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274530 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGD2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274531 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274532 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274533 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13S-HpOTrE, Eicosanoid 9S-HpOTrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274534 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9S-HpOTrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274535 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274536 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274537 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274538 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274539 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17(18) EpETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274540 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274541 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HEPE, Eicosanoid 9(S) HEPE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274542 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12(S) HEPE, Eicosanoid 15(S) HEPE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274543 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274544 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-HETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274545 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 10-Nitrooleate, Eicosanoid 9-Nitrooleate levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274546 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-EET, Eicosanoid 8,9-EET a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274547 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-EET, Eicosanoid 8,9-EET b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274548 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11(12)-EpETE, Eicosanoid 14(15) EpETE, Eicosanoid 15-oxoETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274549 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11(12)-EpETE, Eicosanoid 14(15) EpETE, Eicosanoid 15-oxoETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274550 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-diHETrE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274551 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17-HETE, Eicosanoid 18(+/-)-HETE, Eicosanoid 20-HETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274477 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 19(R)-HETE, Eicosanoid 20-HETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274478 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15(S) HETrE, Eicosanoid 8(S) HETrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274479 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HETrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274480 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274481 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274482 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 14,15-dehydro-LTB4 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274483 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274484 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12oxo LTB4 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274485 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGJ2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274486 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274487 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13,14-dihydro-15-keto-PGA2 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274488 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17,18-DiHETE, Eicosanoid 5,12-DiHETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274489 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274490 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12epi LTB4, Eicosanoid 14,15-DiHETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274491 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274492 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274493 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274494 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1, Eicosanoid PGA1 c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274495 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 d levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274496 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274497 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 13-oxoODE c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274498 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274499 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid HXA3 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274500 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274501 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11,12-diHETrE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274552 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-HETE, Eicosanoid 12-HETE, Eicosanoid 8-HETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274553 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-2,3-dinor-TXB2 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274554 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-2,3-dinor-TXB2 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274555 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274556 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11-dehydro-TXB3 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274557 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11b PGE2, Eicosanoid 15k PGF2a, Eicosanoid PGD2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274558 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11d-TXB2 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274559 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11d-TXB2 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274560 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 11t LTD4 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274561 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpEPE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274562 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274563 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274564 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HpETE c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274565 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME, Eicosanoid 9,10 diHOME a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274566 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12,13 diHOME, Eicosanoid 9,10 diHOME b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274567 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274568 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HETE, Eicosanoid 8-HETE, Eicosanoid 9-HETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274569 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-HHTrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274570 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274571 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274572 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274573 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-OPDA d levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274574 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12S-HEPE, Eicosanoid 15S-HEPE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274575 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 12-oxoETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274576 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274627 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274628 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274629 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-diHETrE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274630 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274631 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274632 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5(S) HETrE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274633 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274634 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5-oxoETE c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274635 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8(S) HETrE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274636 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-15k PGF2b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274637 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGA1 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274638 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 8-iso-PGF1a, Eicosanoid 8-iso-PGF1b, Eicosanoid PGF1beta a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274639 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 EpOME a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274640 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 EpOME b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274641 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9,10 diHOME levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274642 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9(S) HOTrE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274643 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoODE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274644 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 9-oxoOTrE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274645 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Adrenic Acid a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274646 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Adrenic Acid b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274647 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274648 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274649 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Arachidonic Acid c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274650 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. FFA Docosahexaenoic Acid levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274651 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15S-HpETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274602 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274603 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-epi-PGA1, Eicosanoid PGA1 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274604 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15 oxoEDE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274605 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15 oxoEDE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274606 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15-oxoETE, Eicosanoid 17(18) EpETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274607 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGA2 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274608 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGA2 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274609 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGJ2 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274610 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15d PGJ2 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274611 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 15t-Protectin D1 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274612 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 16-HETE, Eicosanoid 17-HETE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274613 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17S-HpDHA d levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274614 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 17S-HpDHA b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274615 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274616 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274617 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 20cooh AA c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274618 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3-dinor-PGE1 a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274619 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3-dinor-PGE1 b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274620 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 2,3 dinor TXB2 levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274621 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpEPE levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274622 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE a levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274623 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE b levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274624 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5S-HpETE c levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274625 Genome-wide genotyping array 2023-10-23 37524825 Rhee EP 2023-07-31 Commun Biol www.ncbi.nlm.nih.gov/pubmed/37524825 A genome-wide association study identifies 41 loci associated with eicosanoid levels. Eicosanoid 5,6-EET levels 6,496 European ancestry individuals NA Affymetrix [8526654] (imputed) 0 ecosanoids measurement http://www.ebi.ac.uk/efo/EFO_0020044 GCST90274626 Genome-wide genotyping array 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Stroke 5,294 European ancestry cases, 17,021 European ancestry controls, 1,022 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 360 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 116 Asian ancestry cases, 734 Asian ancestry controls, 20 Native American ancestry cases, 34 Native American ancestry controls, 21 cases, 216 controls NA NR [40000000] (imputed) 2 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90137416 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Ischemic stroke 4,307 European ancestry cases, 17,021 European ancestry controls, 884 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 316 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 80 Asian ancestry cases, 734 Asian ancestry controls, 12 Native American ancestry cases, 34 Native American ancestry controls, 17 cases, 216 controls 16,851 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry cases, 32,473 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry controls NR [40000000] (imputed) 2 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90137417 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Cardioembolic stroke 1,276 European ancestry cases, 17,021 European ancestry controls, 122 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 39 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 17 Asian ancestry cases, 734 Asian ancestry controls, 5 Native American ancestry cases, 34 Native American ancestry controls, 216 controls 16,851 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry cases, 32,473 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry controls NR [40000000] (imputed) 2 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90137418 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Large artery stroke 296 European ancestry cases, 17,021 European ancestry controls, 33 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 19 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 4 Asian ancestry cases, 734 Asian ancestry controls, 34 Native American ancestry individuals, 216 controls 16,851 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry cases, 32,473 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry controls NR [40000000] (imputed) 1 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90137419 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Small vessel stroke 692 European ancestry cases, 17,021 European ancestry controls, 132 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 43 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 29 Asian ancestry cases, 734 Asian ancestry controls, 2 Native American ancestry cases, 34 Native American ancestry controls, 216 controls 16,851 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry cases, 32,473 European, African American or Afro-Caribbean, Hispanic or Latin American cases, Asian, Native American and unknown ancestry controls NR [40000000] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90137420 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Hemorrhagic stroke 862 European ancestry cases, 17,021 European ancestry controls, 127 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 43 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 36 Asian ancestry cases, 734 Asian ancestry controls, 8 Native American ancestry cases, 34 Native American ancestry controls, 4 cases, 216 controls NA NR [40000000] (imputed) 1 hemorrhagic stroke http://www.ebi.ac.uk/efo/EFO_0020921 GCST90137421 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Intracerebral hemorrhage 592 European ancestry cases, 17,021 European ancestry controls, 68 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 19 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 31 Asian ancestry cases, 734 Asian ancestry controls, 6 Native American ancestry cases, 34 Native American ancestry controls, 216 controls NA NR [40000000] (imputed) 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90137422 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Subarachnoid hemorrhage 167 European ancestry cases, 17,021 European ancestry controls, 26 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls, 9 Hispanic or Latin American cases, 2,256 Hispanic or Latin American controls, 5 Asian ancestry cases, 734 Asian ancestry controls, 1 Native American ancestry cases, 34 Native American ancestry controls, 216 controls NA NR [40000000] (imputed) 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90137423 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Stroke 5,294 European ancestry cases, 17,021 European ancestry controls NA NR [40000000] (imputed) 0 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90137424 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Cardioembolic stroke 1,276 European ancestry cases, 17,021 European ancestry controls up to 16,851 European ancestry cases, up to 32,473 European ancestry controls NR [40000000] (imputed) 0 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90137425 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Large artery stroke 296 European ancestry cases, 17,021 European ancestry controls up to 16,851 European ancestry cases, up to 32,473 European ancestry controls NR [40000000] (imputed) 0 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90137426 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Small vessel stroke 692 European ancestry cases, 17,021 European ancestry controls up to 16,851 European ancestry cases, up to 32,473 European ancestry controls NR [40000000] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90137427 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Hemorrhagic stroke 862 European ancestry cases, 17,021 European ancestry controls NA NR [40000000] (imputed) 0 hemorrhagic stroke http://www.ebi.ac.uk/efo/EFO_0020921 GCST90137428 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Stroke 1,022 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls NA NR [40000000] (imputed) 1 stroke http://www.ebi.ac.uk/efo/EFO_0000712 GCST90137429 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Ischemic stroke 884 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls 1,323 African American or Afro-Caribbean cases, 2,383 African American or Afro-Caribbean controls NR [40000000] (imputed) 2 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90137430 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Cardioembolic stroke 122 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls up to 16,851 African American or Afro-Caribbean cases, up to 32,473 African American or Afro-Caribbean controls NR [40000000] (imputed) 1 cardioembolic stroke http://www.ebi.ac.uk/efo/EFO_1001976 GCST90137431 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Large artery stroke 33 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls up to 16,851 African American or Afro-Caribbean cases, up to 32,473 African American or Afro-Caribbean controls NR [40000000] (imputed) 0 large artery stroke http://www.ebi.ac.uk/efo/EFO_0005524 GCST90137432 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Small vessel stroke 132 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls up to 16,851 African American or Afro-Caribbean cases, up to 32,473 African American or Afro-Caribbean controls NR [40000000] (imputed) 0 small vessel stroke http://www.ebi.ac.uk/efo/EFO_1001504 GCST90137433 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Hemorrhagic stroke 127 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls NA NR [40000000] (imputed) 0 hemorrhagic stroke http://www.ebi.ac.uk/efo/EFO_0020921 GCST90137434 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Intracerebral hemorrhage 68 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls NA NR [40000000] (imputed) 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90137435 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Subarachnoid hemorrhage 26 African American or Afro-Caribbean cases, 6,855 African American or Afro-Caribbean controls NA NR [40000000] (imputed) 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90137436 Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Ischemic stroke 8,781 European ancestry cases, 41,021 European ancestry controls NA Affymetrix [13000000] (imputed) 2 Ischemic stroke http://purl.obolibrary.org/obo/HP_0002140 GCST90137437 Genome-wide genotyping array, Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Intracerebral hemorrhage 1,551 European ancestry cases, 21,821 European ancestry controls NA Affymetrix [13000000] (imputed) 0 intracerebral hemorrhage http://www.ebi.ac.uk/efo/EFO_0005669 GCST90137438 Genome-wide genotyping array, Genome-wide sequencing 2023-11-09 34727735 Hu Y 2021-11-03 Stroke www.ncbi.nlm.nih.gov/pubmed/34727735 Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project. Subarachnoid hemorrhage 1,361 European ancestry cases, 22,991 European ancestry controls NA Affymetrix [13000000] (imputed) 0 subarachnoid hemorrhage http://www.ebi.ac.uk/efo/EFO_0000713 GCST90137439 Genome-wide genotyping array, Genome-wide sequencing 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral accumbens volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006931 GCST90296636 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral accumbens volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006931 GCST90255778 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral accumbens volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006931 GCST90296638 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral accumbens volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006931 GCST90255780 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral amygdala volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, subcortical volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0021790 GCST90296640 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral amygdala volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 subcortical volume measurement http://www.ebi.ac.uk/efo/EFO_0021790 GCST90255782 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral caudate volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0004830 GCST90296642 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral pallidum volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 pallidum volume http://www.ebi.ac.uk/efo/EFO_0006933 GCST90255784 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral putamen volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 putamen volume http://www.ebi.ac.uk/efo/EFO_0006932 GCST90255785 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral thalamus volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST90255786 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral intracranial volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0004886 GCST90255787 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral hippocampus volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, hippocampal volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0005035 GCST90296647 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral amygdala volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, subcortical volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0021790 GCST90255789 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral intracranial volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004886 GCST90296649 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral pallidum volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 pallidum volume, psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006933, http://www.ebi.ac.uk/efo/EFO_0006783 GCST90255791 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral pallidum volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 pallidum volume http://www.ebi.ac.uk/efo/EFO_0006933 GCST90296651 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral thalamus volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, thalamus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006935 GCST90255793 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral pallidum volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 pallidum volume, psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006933, http://www.ebi.ac.uk/efo/EFO_0006783 GCST90296653 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral putamen volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 putamen volume http://www.ebi.ac.uk/efo/EFO_0006932 GCST90296654 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral putamen volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, putamen volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006932 GCST90296655 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral amygdala volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, subcortical volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0021790 GCST90255796 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral thalamus volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 thalamus volume http://www.ebi.ac.uk/efo/EFO_0006935 GCST90296657 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral pallidum volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 pallidum volume, psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006933, http://www.ebi.ac.uk/efo/EFO_0006783 GCST90255798 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral putamen volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, putamen volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006932 GCST90255799 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral thalamus volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, thalamus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006935 GCST90255800 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral intracranial volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004886 GCST90255801 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral thalamus volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, thalamus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006935 GCST90296659 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral accumbens volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006931 GCST90296637 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral caudate volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004830 GCST90255779 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral amygdala volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 subcortical volume measurement http://www.ebi.ac.uk/efo/EFO_0021790 GCST90296639 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral caudate volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0004830 GCST90255781 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral amygdala volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, subcortical volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0021790 GCST90296641 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral hippocampus volume 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90255783 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral caudate volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004830 GCST90296643 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral caudate volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004830 GCST90296644 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral hippocampus volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 hippocampal volume http://www.ebi.ac.uk/efo/EFO_0005035 GCST90296645 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral hippocampus volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, hippocampal volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0005035 GCST90296646 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral accumbens volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, nucleus accumbens volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006931 GCST90255788 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral intracranial volume 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0004886 GCST90296648 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral hippocampus volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, hippocampal volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0005035 GCST90255790 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral intracranial volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004886 GCST90296650 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral putamen volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, putamen volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006932 GCST90255792 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral pallidum volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 pallidum volume, psychosocial stress measurement http://www.ebi.ac.uk/efo/EFO_0006933, http://www.ebi.ac.uk/efo/EFO_0006783 GCST90296652 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral intracranial volume x prenatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, intracranial volume measurement http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004886 GCST90255794 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral caudate volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, caudate nucleus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0004830 GCST90255795 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral putamen volume x postnatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, putamen volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006932 GCST90296656 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral hippocampus volume x postnatal stress interaction 2,257 European or unknown ancestry individuals 10,749 European or unknown ancestry individuals Illumina [8579196] (imputed) 0 psychosocial stress measurement, hippocampal volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0005035 GCST90255797 Genome-wide genotyping array 2023-11-03 36777645 Bolhuis K 2022-11-16 JCPP Adv www.ncbi.nlm.nih.gov/pubmed/36777645 Mapping gene by early life stress interactions on child subcortical brain structures: A genome-wide prospective study. Bilateral thalamus volume x prenatal stress interaction 1,049 European ancestry individuals NA Illumina [7772133] (imputed) 0 psychosocial stress measurement, thalamus volume http://www.ebi.ac.uk/efo/EFO_0006783, http://www.ebi.ac.uk/efo/EFO_0006935 GCST90296658 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup H 112,792 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264121 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup HV 4,687 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264122 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup I 8,024 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264123 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup J 29,463 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264124 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup K 23,131 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264125 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup T 26,893 European ancestry individuals NA Affymetrix [8912253] (imputed) 1 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264126 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup U 37,626 European ancestry individuals NA Affymetrix [8912253] (imputed) 2 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264127 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup V 8,818 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264128 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup W 5,175 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264129 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor anxiety/tension in mitochondrial haplogroup X 3,851 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 anxiety measurement http://www.ebi.ac.uk/efo/EFO_0009863 GCST90264130 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup H 112,792 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264131 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup HV 4,687 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264132 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup I 8,024 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264133 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup J 29,463 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264134 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup K 23,131 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264135 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup T 26,893 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264136 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup U 37,626 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264137 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup V 8,818 European ancestry individuals NA Affymetrix [8912253] (imputed) 1 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264138 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup W 5,175 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264139 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. General factor of neuroticism in mitochondrial haplogroup X 3,851 European ancestry individuals NA Affymetrix [8912253] (imputed) 1 neuroticism measurement http://www.ebi.ac.uk/efo/EFO_0007660 GCST90264140 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup H 112,792 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264141 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup HV 4,687 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264142 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup I 8,024 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264143 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup J 29,463 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264144 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup K 23,131 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264145 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup T 26,893 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264146 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup U 37,626 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264147 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup V 8,818 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264148 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup W 5,175 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264149 Genome-wide genotyping array 2023-07-24 37253732 Xia C 2023-05-30 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37253732 The contributions of mitochondrial and nuclear mitochondrial genetic variation to neuroticism. Special factor worry/vulnerability in mitochondrial haplogroup X 3,851 European ancestry individuals NA Affymetrix [8912253] (imputed) 0 worry measurement http://www.ebi.ac.uk/efo/EFO_0009589 GCST90264150 Genome-wide genotyping array 2023-12-13 37125963 Tam CHT 2023-05-01 Diabetes Care www.ncbi.nlm.nih.gov/pubmed/37125963 Identification of a Common Variant for Coronary Heart Disease at PDE1A Contributes to Individualized Treatment Goals and Risk Stratification of Cardiovascular Complications in Chinese Patients With Type 2 Diabetes. Coronary heart disease in type 2 diabetes 2,517 Southern Han Chinese ancestry cases, 6,424 Southern Han Chinese ancestry controls 1,079 Southern Han Chinese ancestry cases, 2,474 Southern Han Chinese ancestry controls, 764 European ancestry cases, 4,276 European ancestry controls Affymetrix, Illumina [6616004] (imputed) 3 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90281031 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 1) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 13 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270327 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 2) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 3 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270328 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 3) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 2 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270329 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 4) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 1 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270330 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 5) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 4 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270331 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 6) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 0 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270332 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 7) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 0 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270333 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 8) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 1 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270334 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 9) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 0 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270335 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 10) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 0 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270336 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 11) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 4 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270337 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 12) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 1 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270338 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 13) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 0 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270339 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 14) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 0 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270340 Genome-wide genotyping array 2023-11-29 37973980 Goovaerts S 2023-11-16 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37973980 Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape. Cranial vault shape (segment 15) 4,198 European ancestry individuals, 2,574 African American or Afro-Caribbean, Hispanic or Latin American, Sub-Saharan African ancestry individuals NA NR [10647531] (imputed) 1 cranial vault morphology measurement http://www.ebi.ac.uk/efo/EFO_0009278 GCST90270341 Genome-wide genotyping array 2023-11-22 37547536 Downie ML 2023-05-27 Kidney Int Rep www.ncbi.nlm.nih.gov/pubmed/37547536 Common Risk Variants in AHI1 Are Associated With Childhood Steroid Sensitive Nephrotic Syndrome. Pediatric steroid sensitive nephrotic syndrome 420 Sri Lankan ancestry cases, 2,339 Sri Lankan ancestry controls 150 South Asian ancestry cases, 277 South Asian ancestry controls Affymetrix, Illumina [5265125] (imputed) 1 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90297792 Genome-wide genotyping array 2023-11-22 37547536 Downie ML 2023-05-27 Kidney Int Rep www.ncbi.nlm.nih.gov/pubmed/37547536 Common Risk Variants in AHI1 Are Associated With Childhood Steroid Sensitive Nephrotic Syndrome. Pediatric steroid sensitive nephrotic syndrome 420 Sri Lankan ancestry cases, 2,339 Sri Lankan ancestry controls, 422 European ancestry cases, 5,642 European ancestry controls 150 South Asian ancestry cases, 277 South Asian ancestry controls Affymetrix, Illumina [3727716] (imputed) 1 nephrotic syndrome http://www.ebi.ac.uk/efo/EFO_0004255 GCST90297793 Genome-wide genotyping array 2023-08-25 37277458 Vosberg DE 2023-06-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/37277458 The genetics of a "femaleness/maleness" score in cardiometabolic traits in the UK biobank. Multi-trait sex score 161,906 European ancestry females NA Affymetrix [8642454] (imputed) 1373 sexual dimorphism measurement http://www.ebi.ac.uk/efo/EFO_0021796 GCST90270116 Genome-wide genotyping array 2023-08-25 37277458 Vosberg DE 2023-06-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/37277458 The genetics of a "femaleness/maleness" score in cardiometabolic traits in the UK biobank. Multi-trait sum score 161,906 European ancestry females NA Affymetrix [8642454] (imputed) 331 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST90270117 Genome-wide genotyping array 2023-08-25 37277458 Vosberg DE 2023-06-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/37277458 The genetics of a "femaleness/maleness" score in cardiometabolic traits in the UK biobank. Multi-trait sex score 141,980 European ancestry males NA Affymetrix [8644321] (imputed) 1227 sexual dimorphism measurement http://www.ebi.ac.uk/efo/EFO_0021796 GCST90270118 Genome-wide genotyping array 2023-08-25 37277458 Vosberg DE 2023-06-05 Sci Rep www.ncbi.nlm.nih.gov/pubmed/37277458 The genetics of a "femaleness/maleness" score in cardiometabolic traits in the UK biobank. Multi-trait sum score 141,980 European ancestry males NA Affymetrix [8644321] (imputed) 216 complex trait http://www.ebi.ac.uk/efo/EFO_0010578 GCST90270119 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Total alcohol consumption 31,129 Korean ancestry individuals NA NR [8056211] (imputed) 37 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255467 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Diabetes 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 213 diabetes mellitus http://www.ebi.ac.uk/efo/EFO_0000400 GCST90255468 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Lung cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 4 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90255469 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Gastric cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 16 gastric carcinoma http://www.ebi.ac.uk/efo/EFO_0000178 GCST90255470 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Colon cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 13 colon carcinoma http://www.ebi.ac.uk/efo/EFO_1001950 GCST90255471 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Uterine cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 5 uterine carcinoma http://www.ebi.ac.uk/efo/EFO_0002919 GCST90255472 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Breast cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 7 breast carcinoma http://www.ebi.ac.uk/efo/EFO_0000305 GCST90255473 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Thyroid cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 1 thyroid carcinoma http://www.ebi.ac.uk/efo/EFO_0002892 GCST90255474 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Prostate cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 30 prostate carcinoma http://www.ebi.ac.uk/efo/EFO_0001663 GCST90255475 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Systolic blood pressure 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 98 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90255476 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Diastolic blood pressure 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 71 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90255477 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Height 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 1426 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90255478 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Weight 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 422 body weight http://www.ebi.ac.uk/efo/EFO_0004338 GCST90255479 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. BMI 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 280 body mass index http://www.ebi.ac.uk/efo/EFO_0004340 GCST90255480 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hemoglobin A1c levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 101 HbA1c measurement http://www.ebi.ac.uk/efo/EFO_0004541 GCST90255481 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Glucose levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 104 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90255482 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Blood urea nitrogen levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 167 blood urea nitrogen measurement http://www.ebi.ac.uk/efo/EFO_0004741 GCST90255483 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Albumin levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 118 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90255484 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Creatinine levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 236 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90255485 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Aspartate aminotransferase levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 173 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90255486 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Total bilirubin levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 116 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90255487 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Alanine aminotransferase levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 124 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90255488 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Total cholesterol levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 226 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90255489 Genome-wide genotyping array 2023-06-23 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Gamma-glutamyl transpeptidase levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 316 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90255490 Genome-wide genotyping array 2023-06-23 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. HDL cholesterol levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 366 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90255491 Genome-wide genotyping array 2023-11-17 37236969 Shi J 2023-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37236969 Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. Lung adenocarcinoma 11,753 East Asian ancestry cases, 30,562 East Asian ancestry controls 9,905 East Asian ancestry cases, 120,114 East Asian ancestry controls Affymetrix, Illumina [NR] (imputed) 11 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST90297562 Genome-wide genotyping array 2023-11-17 37236969 Shi J 2023-05-26 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37236969 Genome-wide association study of lung adenocarcinoma in East Asia and comparison with a European population. Lung adenocarcinoma 11,753 East Asian ancestry cases, 30,562 East Asian ancestry controls, 11,273 European ancestry cases, 55,483 European ancestry controls NA Affymetrix, Illumina [NR] (imputed) 6 lung adenocarcinoma http://www.ebi.ac.uk/efo/EFO_0000571 GCST90297563 Genome-wide genotyping array 2023-11-16 37236919 Ou YN 2023-05-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37236919 The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Fornix white matter microstructure (fractional anisotropy) 30,832 British ancestry individuals 3,613 European ancestry individuals NR [NR] 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90297552 Genome-wide genotyping array 2023-11-16 37236919 Ou YN 2023-05-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37236919 The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Fornix white matter microstructure (mean diusivities) 30,832 British ancestry individuals 3,613 European ancestry individuals NR [NR] 0 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90297553 Genome-wide genotyping array 2023-11-16 37236919 Ou YN 2023-05-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37236919 The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Fornix white matter microstructure (diffusion tensor mode) 30,832 British ancestry individuals NA NR [NR] 8 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90297554 Genome-wide genotyping array 2023-11-16 37236919 Ou YN 2023-05-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37236919 The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Fornix white matter microstructure (orientation dispersion index) 30,832 British ancestry individuals NA NR [NR] 2 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90297555 Genome-wide genotyping array 2023-11-16 37236919 Ou YN 2023-05-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37236919 The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Fornix white matter microstructure (intra-cellular volume fraction) 30,832 British ancestry individuals NA NR [NR] 23 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90297556 Genome-wide genotyping array 2023-11-16 37236919 Ou YN 2023-05-26 Transl Psychiatry www.ncbi.nlm.nih.gov/pubmed/37236919 The genetic architecture of fornix white matter microstructure and their involvement in neuropsychiatric disorders. Fornix white matter microstructure (isotropic or free water volume fraction) 30,832 British ancestry individuals NA NR [NR] 22 white matter microstructure measurement http://www.ebi.ac.uk/efo/EFO_0005674 GCST90297557 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Phosphorus intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 1 dietary phosphorus intake measurement http://www.ebi.ac.uk/efo/EFO_0020091 GCST90255442 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Iron intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary heme iron intake measurement http://www.ebi.ac.uk/efo/EFO_0008355 GCST90255443 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Potassium intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary potassium intake measurement http://www.ebi.ac.uk/efo/EFO_0008470 GCST90255444 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Vitamin A intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary vitamin A intake measurement http://www.ebi.ac.uk/efo/EFO_0020077 GCST90255445 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Sodium intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 1 dietary sodium intake measurement http://www.ebi.ac.uk/efo/EFO_0020080 GCST90255446 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Vitamin B1 intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 1 dietary vitamin B1 intake measurement http://www.ebi.ac.uk/efo/EFO_0020078 GCST90255447 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Vitamin B2 intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 2 dietary vitamin B2 intake measurement http://www.ebi.ac.uk/efo/EFO_0020079 GCST90255448 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Niacin intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary niacin intake measurement http://www.ebi.ac.uk/efo/EFO_0020081 GCST90255449 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Vitamin C intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary vitamin C intake measurement http://www.ebi.ac.uk/efo/EFO_0020082 GCST90255450 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Zinc intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 1 dietary zinc intake measurement http://www.ebi.ac.uk/efo/EFO_0020083 GCST90255451 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Vitamin B6 intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary vitamin B6 intake measurement http://www.ebi.ac.uk/efo/EFO_0020084 GCST90255452 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Folate intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 folate intake measurement http://www.ebi.ac.uk/efo/EFO_0800000 GCST90255453 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Retinol intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary retinol intake measurement http://www.ebi.ac.uk/efo/EFO_0020085 GCST90255454 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Carotene intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary carotene intake measurement http://www.ebi.ac.uk/efo/EFO_0020086 GCST90255455 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Ash intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary ash intake measurement http://www.ebi.ac.uk/efo/EFO_0020087 GCST90255456 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Fiber intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary fiber intake measurement http://www.ebi.ac.uk/efo/EFO_0020088 GCST90255457 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Vitamin E intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary vitamin E intake measurement http://www.ebi.ac.uk/efo/EFO_0020089 GCST90255458 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Cholesterol intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 dietary cholesterol intake measurement http://www.ebi.ac.uk/efo/EFO_0020090 GCST90255459 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Drinking duration 33,398 Korean ancestry individuals NA NR [8056211] (imputed) 4 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255460 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Makgeolli frequency 72,167 Korean ancestry individuals NA NR [8056211] (imputed) 37 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255461 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Sake frequency 72,184 Korean ancestry individuals NA NR [8056211] (imputed) 1 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255462 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Wine frequency 72,181 Korean ancestry individuals NA NR [8056211] (imputed) 4 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255463 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Soju frequency 72,151 Korean ancestry individuals NA NR [8056211] (imputed) 102 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255464 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Beer frequency 72,165 Korean ancestry individuals NA NR [8056211] (imputed) 54 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255465 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hard liquor frequency 72,178 Korean ancestry individuals NA NR [8056211] (imputed) 1 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90255466 Genome-wide genotyping array 2023-12-14 37345113 Verma SS 2023-05-16 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/37345113 Genome-Wide Association Study of Breast Density among Women of African Ancestry. Breast area 1,333 African American individuals NA NR [NR] 63 GCST90293090 Genome-wide genotyping array 2023-12-14 37345113 Verma SS 2023-05-16 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/37345113 Genome-Wide Association Study of Breast Density among Women of African Ancestry. Breast dense area 1,333 African American individuals NA NR [NR] 411 GCST90293091 Genome-wide genotyping array 2023-12-14 37345113 Verma SS 2023-05-16 Cancers (Basel) www.ncbi.nlm.nih.gov/pubmed/37345113 Genome-Wide Association Study of Breast Density among Women of African Ancestry. Breast area percent density 1,333 African American individuals NA NR [NR] 175 GCST90293092 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. LDL cholesterol levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 157 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90255492 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Triglyceride levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 253 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90255493 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. White blood cell count 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 267 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90255494 Genome-wide genotyping array 2023-06-23 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Red blood cell count 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 342 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90255495 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hematocrit levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 145 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90255496 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hemoglobin levels 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 158 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90255497 Genome-wide genotyping array 2023-06-23 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Platelet count 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 531 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90255498 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Pancreatic cancer 251,000 East Asian ancestry individuals NA NR [6907490] (imputed) 0 pancreatic carcinoma http://www.ebi.ac.uk/efo/EFO_0002618 GCST90255499 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Sepsis (death vs survived) 1,896 European ancestry sepsis death cases, 9,747 European ancestry sepsis cases NA Illumina [12370774] (imputed) 0 Sepsis, mortality http://purl.obolibrary.org/obo/HP_0100806, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281180 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Cellulitis 12,196 European ancestry cases, 474,288 European ancestry controls NA Illumina [12370750] (imputed) 0 cellulitis http://www.ebi.ac.uk/efo/EFO_0003035 GCST90281156 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Urinary tract infection 21,958 European ancestry cases, 464,526 European ancestry controls NA Illumina [12370776] (imputed) 0 urinary tract infection http://www.ebi.ac.uk/efo/EFO_0003103 GCST90281182 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Sepsis (aged <75) 11,568 European ancestry cases, 462,869 European ancestry controls NA Illumina [12370777] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90281183 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Endocarditis 1,080 European ancestry cases, 485,404 European ancestry controls NA Illumina [12370752] (imputed) 0 endocarditis http://www.ebi.ac.uk/efo/EFO_0000465 GCST90281158 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Lower repsiratory tract infection 14,135 European ancestry cases, 472,349 European ancestry controls NA Illumina [12370753] (imputed) 0 lower respiratory tract disease http://www.ebi.ac.uk/efo/EFO_0009433 GCST90281159 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical lower repsiratory tract infection death 50 European ancestry cases, 431,315 European ancestry controls NA Illumina [12370754] (imputed) 0 lower respiratory tract disease, mortality http://www.ebi.ac.uk/efo/EFO_0009433, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281160 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical lower repsiratory tract infection death (death vs survived) 50 European ancestry critical lower repsiratory tract infection death cases, 535 European ancestry critical lower repsiratory tract infection cases NA Illumina [12370755] (imputed) 0 lower respiratory tract disease, mortality http://www.ebi.ac.uk/efo/EFO_0009433, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281161 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical lower respiratory tract infection 585 European ancestry cases, 430,780 European ancestry controls NA Illumina [12370756] (imputed) 0 lower respiratory tract disease http://www.ebi.ac.uk/efo/EFO_0009433 GCST90281162 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical lower respiratory tract infection vs lower repsiratory tract infection 585 European ancestry critical lower respiratory tract infection cases, 13,050 European ancestry lower respiratory tract infection cases NA Illumina [12370757] (imputed) 0 lower respiratory tract disease http://www.ebi.ac.uk/efo/EFO_0009433 GCST90281163 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Lower respiratory tract infection death 702 European ancestry cases, 485,782 European ancestry controls NA Illumina [12370758] (imputed) 0 lower respiratory tract disease, mortality http://www.ebi.ac.uk/efo/EFO_0009433, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281164 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Lower repsiratory tract infection death (death vs survived) 702 European ancestry lower respiratory tract infection death cases, 13,433 European ancestry lower respiratory tract infection cases NA Illumina [12370759] (imputed) 0 lower respiratory tract disease, mortality http://www.ebi.ac.uk/efo/EFO_0009433, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281165 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Osteomyelitis 4,836 European ancestry cases, 481,648 European ancestry controls NA Illumina [12370760] (imputed) 0 osteomyelitis http://www.ebi.ac.uk/efo/EFO_0003102 GCST90281166 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Pneumonia 22,567 European ancestry cases, 469,317 European ancestry controls NA Illumina [12370761] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90281167 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical pneumonia (28-day mortality) 545 European ancestry cases, 430,820 European ancestry controls NA Illumina [12370762] (imputed) 0 pneumonia, mortality http://www.ebi.ac.uk/efo/EFO_0003106, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281168 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical pneumonia (death vs survived) 545 European ancestry critical pneumonia death cases, 2,213 European ancestry critical pneumonia cases NA Illumina [12370763] (imputed) 0 pneumonia, mortality http://www.ebi.ac.uk/efo/EFO_0003106, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281169 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical pneumonia 2,758 European ancestry cases, 428,607 European ancestry controls NA Illumina [12370764] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90281170 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical pneumonia vs pneumonia 2,758 European ancestry critical pneumonia cases, 19,141 European ancestry pneumonia cases NA Illumina [12370765] (imputed) 0 pneumonia http://www.ebi.ac.uk/efo/EFO_0003106 GCST90281171 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Pneumonia (28-day mortality) 3,185 European ancestry cases, 483,299 European ancestry controls NA Illumina [12370766] (imputed) 0 pneumonia, mortality http://www.ebi.ac.uk/efo/EFO_0003106, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281172 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Pneumonia death (death vs survived) 3,185 European ancestry pneumonia death cases, 19,382 European ancestry pneumonia cases NA Illumina [12370767] (imputed) 0 pneumonia, mortality http://www.ebi.ac.uk/efo/EFO_0003106, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281173 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Sepsis (hospital admission) 11,643 European ancestry cases, 47,481 European ancestry controls NA Illumina [12370768] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90281174 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical sepsis (28-day mortality) 347 European ancestry cases, 431,081 European ancestry controls NA Illumina [12370769] (imputed) 0 Sepsis, mortality http://purl.obolibrary.org/obo/HP_0100806, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281175 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical sepsis (death vs survived) 347 European ancestry critical sepsis death cases, 1,033 European ancestry critical sepsis cases NA Illumina [12370770] (imputed) 0 Sepsis, mortality http://purl.obolibrary.org/obo/HP_0100806, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281176 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical sepsis 1,380 European ancestry cases, 429,985 European ancestry controls NA Illumina [12370771] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90281177 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Critical sepsis vs sepsis 1,380 European ancestry critical sepsis cases, 9,981 European ancestry sepsis cases NA Illumina [12370772] (imputed) 0 Sepsis http://purl.obolibrary.org/obo/HP_0100806 GCST90281178 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Sepsis (28-day mortality) 1,896 European ancestry cases, 484,588 European ancestry controls NA Illumina [12370773] (imputed) 0 Sepsis, mortality http://purl.obolibrary.org/obo/HP_0100806, http://www.ebi.ac.uk/efo/EFO_0004352 GCST90281179 Genome-wide genotyping array 2023-09-07 36750733 Silveira PP 2023-02-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36750733 A sex-specific genome-wide association study of depression phenotypes in UK Biobank. Depression (broad) 96,989 European ancestry cases, 177,152 European ancestry controls NA NR [7351435] (imputed) 31 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90281043 Genome-wide genotyping array 2023-09-07 36750733 Silveira PP 2023-02-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36750733 A sex-specific genome-wide association study of depression phenotypes in UK Biobank. Depression (broad) 62,066 European ancestry female cases, 84,208 European ancestry female controls NA NR [7351435] (imputed) 15 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90281044 Genome-wide genotyping array 2023-09-07 36750733 Silveira PP 2023-02-07 Mol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36750733 A sex-specific genome-wide association study of depression phenotypes in UK Biobank. Depression (broad) 34,923 European ancestry male cases, 92,944 European ancestry male controls NA NR [7351435] (imputed) 6 unipolar depression http://www.ebi.ac.uk/efo/EFO_0003761 GCST90281045 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Appendicitis 4,604 European ancestry cases, 481,880 European ancestry controls NA Illumina [12370749] (imputed) 0 appendicitis http://www.ebi.ac.uk/efo/EFO_0007149 GCST90281155 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Upper respiratory tract infection 2,795 European ancestry cases, 483,689 European ancestry controls NA Illumina [12370775] (imputed) 0 upper respiratory tract disorder http://purl.obolibrary.org/obo/MONDO_0004867 GCST90281181 Genome-wide genotyping array 2023-09-20 36716318 Hamilton FW 2023-01-30 PLoS Med www.ncbi.nlm.nih.gov/pubmed/36716318 Therapeutic potential of IL6R blockade for the treatment of sepsis and sepsis-related death: A Mendelian randomisation study. Cholecystitis 4,052 European ancestry cases, 482,432 European ancestry controls NA Illumina [12370751] (imputed) 0 Cholecystitis http://purl.obolibrary.org/obo/HP_0001082 GCST90281157 Genome-wide genotyping array 2023-11-21 37211199 Rayinda T 2023-05-19 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/37211199 Shared Genetic Risk Variants in Both Male and Female Frontal Fibrosing Alopecia. Frontal fibrosing alopecia 92 European ancestry male cases, 330 European ancestry male controls NA Illumina [17307641] (imputed) 1 frontal fibrosing alopecia http://www.ebi.ac.uk/efo/EFO_0009855 GCST90264153 Genome-wide genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Diastolic blood pressure 810,865 European ancestry individuals NA Affymetrix, Illumina [242866] (imputed) 158 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90000059 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Hypertension 810,865 European ancestry individuals NA Affymetrix, Illumina [239843] (imputed) 32 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90000060 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Pulse pressure 810,865 European ancestry individuals NA Affymetrix, Illumina [242866] (imputed) 149 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90000061 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Systolic blood pressure 810,865 European ancestry individuals NA Affymetrix, Illumina [242865] (imputed) 176 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90000062 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Diastolic blood pressure 810,865 European ancestry individuals, 21,077 African American individuals, 33,689 South Asian ancestry individuals, 4,586 Hispanic individuals NA Affymetrix, Illumina [247314] (imputed) 13 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90000063 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Hypertension 810,865 European ancestry individuals, 21,077 African American individuals, 33,689 South Asian ancestry individuals, 4,586 Hispanic individuals NA Affymetrix, Illumina [246710] (imputed) 4 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90000064 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Pulse pressure 810,865 European ancestry individuals, 21,077 African American individuals, 33,689 South Asian ancestry individuals, 4,586 Hispanic individuals NA Affymetrix, Illumina [247315] (imputed) 16 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90000065 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Systolic blood pressure 810,865 European ancestry individuals, 21,077 African American individuals, 33,689 South Asian ancestry individuals, 4,586 Hispanic individuals NA Affymetrix, Illumina [247314] (imputed) 14 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90000066 Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Diastolic blood pressure 670,472 European ancestry individuals NA Affymetrix [29454246] (imputed) 12 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST012378 Genome-wide genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Pulse pressure 670,472 European ancestry individuals NA Illumina [29454246] (imputed) 18 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST012377 Genome-wide genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Systolic blood pressure 670,472 European ancestry individuals NA Affymetrix [29454246] (imputed) 18 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST012376 Genome-wide genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Diastolic blood pressure 1,164,961 European ancestry individuals NA Affymetrix, Illumina [1160000] (imputed) 160 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90292474 Genome-wide genotyping array, Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Hypertension 1,164,961 European ancestry individuals NA Affymetrix, Illumina [1160000] (imputed) 37 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90292475 Genome-wide genotyping array, Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Pulse pressure 1,164,961 European ancestry individuals NA Affymetrix, Illumina [1160000] (imputed) 156 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90292476 Genome-wide genotyping array, Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Systolic blood pressure 1,164,961 European ancestry individuals NA Affymetrix, Illumina [1160000] (imputed) 179 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90292477 Genome-wide genotyping array, Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Diastolic blood pressure 1,164,961 European ancestry individuals, 84,359 African American individuals, 33,689 South Asian ancestry individuals, 27,388 Hispanic individuals, 2,695 Native American ancestry individuals, 4,792 East Asian ancestry individuals NA Affymetrix, Illumina [1319000] (imputed) 13 diastolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006336 GCST90292478 Genome-wide genotyping array, Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Hypertension 1,164,961 European ancestry individuals, 84,359 African American individuals, 33,689 South Asian ancestry individuals, 27,388 Hispanic individuals, 2,695 Native American ancestry individuals, 4,792 East Asian ancestry individuals NA Affymetrix, Illumina [1319000] (imputed) 11 hypertension http://www.ebi.ac.uk/efo/EFO_0000537 GCST90292479 Genome-wide genotyping array, Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Pulse pressure 1,164,961 European ancestry individuals, 84,359 African American individuals, 33,689 South Asian ancestry individuals, 27,388 Hispanic individuals, 2,695 Native American ancestry individuals, 4,792 East Asian ancestry individuals NA Affymetrix, Illumina [1319000] (imputed) 17 pulse pressure measurement http://www.ebi.ac.uk/efo/EFO_0005763 GCST90292480 Genome-wide genotyping array, Exome genotyping array 2023-09-21 33230300 Surendran P 2020-11-23 Nat Genet www.ncbi.nlm.nih.gov/pubmed/33230300 Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals. Systolic blood pressure 1,164,961 European ancestry individuals, 84,359 African American individuals, 33,689 South Asian ancestry individuals, 27,388 Hispanic individuals, 2,695 Native American ancestry individuals, 4,792 East Asian ancestry individuals NA Affymetrix, Illumina [1319000] (imputed) 15 systolic blood pressure http://www.ebi.ac.uk/efo/EFO_0006335 GCST90292481 Genome-wide genotyping array, Exome genotyping array 2023-10-06 37188663 Ollila HM 2023-05-15 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37188663 Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy. Type 1 narcolepsy 213 African American or Afro-Caribbean cases, 1,747 African American or Afro-Caribbean controls, 2,412 East Asian ancestry cases, 5,902 East Asian ancestry controls, 3,448 European ancestry cases, 77,207 European ancestry controls NA Affymetrix [12600187] (imputed) 13 narcolepsy-cataplexy syndrome http://purl.obolibrary.org/obo/MONDO_0016158 GCST90293089 Genome-wide genotyping array 2023-12-14 25891430 Li J 2015-04-20 Nat Commun www.ncbi.nlm.nih.gov/pubmed/25891430 Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. Common variable immunodeficiency 778 European ancestry cases, 10,999 European ancestry controls NA Illumina [123127] (imputed) 6 common variable immunodeficiency http://purl.obolibrary.org/obo/MONDO_0015517 GCST90301675 Targeted genotyping array [Immunochip] 2023-10-16 36780644 Oldham JM 2023-02-13 Am J Respir Crit Care Med www.ncbi.nlm.nih.gov/pubmed/36780644 PCSK6 and Survival in Idiopathic Pulmonary Fibrosis. Transplantation-free survival in idiopathic pulmonary fibrosis 1,481 European ancestry individuals 397 European ancestry individuals Affymetrix [9075629] (imputed) 4 event free survival time, idiopathic pulmonary fibrosis http://www.ebi.ac.uk/efo/EFO_0000482, http://www.ebi.ac.uk/efo/EFO_0000768 GCST90295971 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Genital aphthosis in Behcet's disease 367 cases, 68 controls NA Illumina [1416102] (imputed) 3 Abnormality of the genital system http://purl.obolibrary.org/obo/HP_0000078 GCST90301372 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Pseudo-folliculitis in Behcet's disease 318 cases, 113 controls NA Illumina [1416102] (imputed) 0 folliculitis http://www.ebi.ac.uk/efo/EFO_1000702 GCST90301373 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Erythema nodosum in Behcet's disease 233 cases, 203 controls NA Illumina [1416102] (imputed) 1 Erythema nodosum http://purl.obolibrary.org/obo/HP_0012219 GCST90301374 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Ocular lesions in Behcet's disease 191 cases, 245 controls NA Illumina [1416102] (imputed) 2 Abnormality of the eye http://purl.obolibrary.org/obo/HP_0000478 GCST90301375 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Gastrointestinal involvement in Behcet's disease 11 cases, 425 controls NA Illumina [1416102] (imputed) 1 Abnormality of the gastrointestinal tract http://purl.obolibrary.org/obo/HP_0011024 GCST90301376 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Neurological involvement in Behcet's disease 180 cases, 255 controls NA Illumina [1416102] (imputed) 3 Abnormality of the nervous system http://purl.obolibrary.org/obo/HP_0000707 GCST90301377 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Arthritis in Behcet's disease 52 cases, 383 controls NA Illumina [1416102] (imputed) 1 arthritis http://www.ebi.ac.uk/efo/EFO_0005856 GCST90301378 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Vascular involvement in Behcet's disease 124 cases, 311 controls NA Illumina [1416102] (imputed) 0 Abnormality of the vasculature http://purl.obolibrary.org/obo/HP_0002597 GCST90301379 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Arterial involvement in Behcet's disease 21 cases, 409 controls NA Illumina [1416102] (imputed) 2 Abnormal aortic morphology http://purl.obolibrary.org/obo/HP_0001679 GCST90301380 Genome-wide genotyping array 2023-12-06 37271218 Casares-Marfil D 2023-06-02 Clin Immunol www.ncbi.nlm.nih.gov/pubmed/37271218 Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement. Venous involvement in Behcet's disease 107 cases, 322 controls NA Illumina [1416102] (imputed) 0 Abnormal venous morphology http://purl.obolibrary.org/obo/HP_0002624 GCST90301381 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. HDL cholesterol levels 31,565 European ancestry individuals NA NR [7666566] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90025941 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. LDL cholesterol levels 30,509 European ancestry individuals NA NR [7666566] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90025942 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Total cholesterol levels 31,575 European ancestry individuals NA NR [7666566] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90025943 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Triglyceride levels 31,074 European ancestry individuals NA NR [7666566] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90025944 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. HDL cholesterol levels 329,480 European ancestry individuals NA NR [8284910] (imputed) 0 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90301386 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. LDL cholesterol levels 358,482 European ancestry individuals NA NR [8284910] (imputed) 0 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90301387 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Total cholesterol levels 359,096 European ancestry individuals NA NR [8284910] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90301388 Genome-wide genotyping array 2023-12-06 34140684 Veturi Y 2021-06-17 Nat Genet www.ncbi.nlm.nih.gov/pubmed/34140684 A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Triglyceride levels 357,709 European ancestry individuals NA NR [8284910] (imputed) 0 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90301389 Genome-wide genotyping array 2023-10-13 37024583 Naqvi S 2023-04-06 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37024583 Precise modulation of transcription factor levels identifies features underlying dosage sensitivity. Pierre Robin Sequence endophenotypic score 8,246 European ancestry individuals NA NR [7417619] (imputed) 22 facial morphology measurement http://www.ebi.ac.uk/efo/EFO_0007841 GCST90245763 Genome-wide genotyping array 2023-09-04 37055258 Clark R 2023-04-04 EBioMedicine www.ncbi.nlm.nih.gov/pubmed/37055258 A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration. Spherical equivalent refractive error averaged between the 2 eyes (MTAG) 468,769 European ancestry individuals NA NR [958542] 0 refractive error measurement http://www.ebi.ac.uk/efo/EFO_0007814 GCST90275204 Genome-wide genotyping array 2023-12-06 37679419 Lagou V 2023-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37679419 GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Random glucose levels 458,862 European ancestry individuals NA NR [8085507] (imputed) 142 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90271557 Genome-wide genotyping array 2023-12-06 37679419 Lagou V 2023-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37679419 GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Random glucose levels 7,644 African ancestry individuals, 1,503 Chinese ancestry individuals, 7,407 Indian, Pakistani ancestry individuals, 458,862 European ancestry individuals NA NR [8085507] (imputed) 142 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90271558 Genome-wide genotyping array 2023-12-06 37679419 Lagou V 2023-09-07 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37679419 GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Random glucose levels 405,686 European ancestry individuals NA NR [8085507] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90271559 Genome-wide genotyping array 2023-10-12 37688361 Tavares LC 2023-09-08 United European Gastroenterol J www.ncbi.nlm.nih.gov/pubmed/37688361 A pilot genome-wide association study meta-analysis of gastroparesis. Gastroparesis 880 European ancestry cases, 58,271 European ancestry controls NA Illumina [5811784] (imputed) 9 gastroparesis http://www.ebi.ac.uk/efo/EFO_1000948 GCST90295922 Genome-wide genotyping array 2023-10-20 36738982 Tsetsos F 2023-02-02 Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/36738982 Genome-wide Association Study points to novel locus for Gilles de la Tourette Syndrome. Tourette syndrome 6,133 European ancestry cases, 13,565 European ancestry controls NA Illumina [1955677] (imputed) 4 Tourette syndrome http://www.ebi.ac.uk/efo/EFO_0004895 GCST90295972 Genome-wide genotyping array 2023-11-22 37294081 Ang KC 2023-06-09 Elife www.ncbi.nlm.nih.gov/pubmed/37294081 Native American genetic ancestry and pigmentation allele contributions to skin color in a Caribbean population. Skin pigmentation 358 Kalinago ancestry individuals NA Illumina [1638140] (imputed) 3 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90269962 Genome-wide genotyping array 2023-11-22 37294081 Ang KC 2023-06-09 Elife www.ncbi.nlm.nih.gov/pubmed/37294081 Native American genetic ancestry and pigmentation allele contributions to skin color in a Caribbean population. Skin pigmentation 358 Kalinago ancestry individuals NA Illumina [1638140] (imputed) 3 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90269963 Genome-wide genotyping array 2023-11-22 37294081 Ang KC 2023-06-09 Elife www.ncbi.nlm.nih.gov/pubmed/37294081 Native American genetic ancestry and pigmentation allele contributions to skin color in a Caribbean population. Skin pigmentation 358 Kalinago ancestry individuals NA Illumina [1638140] (imputed) 3 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90269964 Genome-wide genotyping array 2023-11-22 37294081 Ang KC 2023-06-09 Elife www.ncbi.nlm.nih.gov/pubmed/37294081 Native American genetic ancestry and pigmentation allele contributions to skin color in a Caribbean population. Skin pigmentation 358 Kalinago ancestry individuals NA Illumina [1638140] (imputed) 3 skin pigmentation measurement http://www.ebi.ac.uk/efo/EFO_0007009 GCST90269965 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Primary aldosteronism 562 European ancestry cases, 950 European ancestry controls 600 European ancestry cases, 2,346 European ancestry controls Illumina [638897] 4 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90129615 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Primary aldosteronism 339 European ancestry male cases, 639 European ancestry male controls 380 European ancestry male cases, 1,228 European ancestry male controls Illumina [629517] 5 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90129616 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Primary aldosteronism 233 European ancestry female cases, 311 European ancestry female controls 220 European ancestry female cases, 1,100 European ancestry female controls Illumina [622710] 3 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90129617 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Aldosterone producing adenoma 321 European ancestry cases, 950 European ancestry controls 354 European ancestry cases, 2,346 European ancestry controls Illumina [628667] 4 aldosterone-producing adenoma http://www.ebi.ac.uk/efo/EFO_1000015 GCST90129618 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Bilateral adrenal hyperplasia 240 European ancestry cases, 950 European ancestry controls 196 European ancestry cases, 2,346 European ancestry controls Illumina [623032] 4 hyperplasia http://www.ebi.ac.uk/efo/EFO_0000536 GCST90129619 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Primary aldosteronism 562 European ancestry cases, 950 European ancestry controls NA Illumina [8301121] (imputed) 0 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90129620 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Primary aldosteronism 339 European ancestry male cases, 639 European ancestry male controls NA Illumina [8328729] (imputed) 0 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90129621 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Primary aldosteronism 233 European ancestry female cases, 311 European ancestry female controls NA Illumina [8348875] (imputed) 0 primary aldosteronism http://purl.obolibrary.org/obo/MONDO_0001422 GCST90129622 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Aldosterone producing adenoma 321 European ancestry cases, 950 European ancestry controls NA Illumina [8305619] (imputed) 0 aldosterone-producing adenoma http://www.ebi.ac.uk/efo/EFO_1000015 GCST90129623 Genome-wide genotyping array 2023-09-05 36057693 Le Floch E 2022-09-03 Nat Commun www.ncbi.nlm.nih.gov/pubmed/36057693 Identification of risk loci for primary aldosteronism in genome-wide association studies. Bilateral adrenal hyperplasia 240 European ancestry cases, 950 European ancestry controls NA Illumina [8307975] (imputed) 0 hyperplasia http://www.ebi.ac.uk/efo/EFO_0000536 GCST90129624 Genome-wide genotyping array 2023-12-07 35915156 Tcheandjieu C 2022-08-01 Nat Med www.ncbi.nlm.nih.gov/pubmed/35915156 Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. Coronary artery disease 190,493 European ancestry cases, 582,775 European ancestry controls NA Affymetrix [NR] (imputed) 33 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90132302 Genome-wide genotyping array 2023-12-07 35915156 Tcheandjieu C 2022-08-01 Nat Med www.ncbi.nlm.nih.gov/pubmed/35915156 Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. Coronary artery disease 12,117 Hispanic or Latin American cases, 44,853 Hispanic or Latin American controls NA Affymetrix [NR] (imputed) 306 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90132303 Genome-wide genotyping array 2023-12-07 35915156 Tcheandjieu C 2022-08-01 Nat Med www.ncbi.nlm.nih.gov/pubmed/35915156 Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. Coronary artery disease 27,021 African American or Afro-Caribbean cases, 102,305 African American or Afro-Caribbean controls NA Affymetrix [NR] (imputed) 134 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90132304 Genome-wide genotyping array 2023-12-07 35915156 Tcheandjieu C 2022-08-01 Nat Med www.ncbi.nlm.nih.gov/pubmed/35915156 Large-scale genome-wide association study of coronary artery disease in genetically diverse populations. Coronary artery disease 190,493 European ancestry cases, 582,775 European ancestry controls, 6,378 Hispanic or Latin American cases, 24,270 Hispanic or Latin American controls, 1,702 African American or Afro-Caribbean cases, 59,507 African American or Afro-Caribbean controls, 29,319 East Asian ancestry cases, 183,134 East Asian ancestry controls NA Affymetrix [NR] (imputed) 62 coronary artery disease http://www.ebi.ac.uk/efo/EFO_0001645 GCST90132305 Genome-wide genotyping array 2023-12-06 37273234 Bhatraju PK 2023-06-05 Kidney360 www.ncbi.nlm.nih.gov/pubmed/37273234 Genome-wide Association Study for Acute Kidney Injury. Acute kidney injury 512 European ancestry cases, 619 European ancestry controls, 87 African ancestry cases, 71 African ancestry controls, 38 cases, 42 controls NA Illumina [8669569] (imputed) 9 Acute kidney injury http://purl.obolibrary.org/obo/HP_0001919 GCST90301382 Genome-wide genotyping array 2023-10-24 36967705 Munday RM 2023-03-27 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/36967705 Genome-wide association studies of diarrhea frequency and duration in the first year of life in Bangladeshi infants. Childhood diarrhea (high frequency) 293 Bangladeshi ancestry infant cases, 90 Bangladeshi ancestry infant controls NA Illumina [7360000] (imputed) 3 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST90296326 Genome-wide genotyping array 2023-10-24 36967705 Munday RM 2023-03-27 J Infect Dis www.ncbi.nlm.nih.gov/pubmed/36967705 Genome-wide association studies of diarrhea frequency and duration in the first year of life in Bangladeshi infants. Childhood diarrhea (prolonged duration) 293 Bangladeshi ancestry infant cases, 90 Bangladeshi ancestry infant controls NA Illumina [7360000] (imputed) 4 Diarrhea http://purl.obolibrary.org/obo/HP_0002014 GCST90296327 Genome-wide genotyping array 2023-09-07 37146673 Grover S 2023-05-03 Int J Infect Dis www.ncbi.nlm.nih.gov/pubmed/37146673 First genome-wide association study for lymphatic filariasis in a West African population points to an HLA-mediated disease pathophysiology. Lymphatic filariasis 1,459 Ghanaian ancestry cases, 1,492 Ghanaian ancestry controls NA Illumina [5592510] (imputed) 3 filarial elephantiasis http://www.ebi.ac.uk/efo/EFO_0007272 GCST90281189 Genome-wide genotyping array 2023-09-07 37146673 Grover S 2023-05-03 Int J Infect Dis www.ncbi.nlm.nih.gov/pubmed/37146673 First genome-wide association study for lymphatic filariasis in a West African population points to an HLA-mediated disease pathophysiology. Lymphatic filariasis with lymphedema 1,166 Ghanaian ancestry cases, 1,492 Ghanaian ancestry controls NA Illumina [5592510] (imputed) 4 lymphedema, filarial elephantiasis http://purl.obolibrary.org/obo/MONDO_0019297, http://www.ebi.ac.uk/efo/EFO_0007272 GCST90281190 Genome-wide genotyping array 2023-09-07 37146673 Grover S 2023-05-03 Int J Infect Dis www.ncbi.nlm.nih.gov/pubmed/37146673 First genome-wide association study for lymphatic filariasis in a West African population points to an HLA-mediated disease pathophysiology. Lymphatic filariasis with hydrocele 278 Ghanaian ancestry male cases, 1,492 Ghanaian ancestry controls NA Illumina [5592510] (imputed) 1 testicular hydrocele, filarial elephantiasis http://www.ebi.ac.uk/efo/EFO_1001859, http://www.ebi.ac.uk/efo/EFO_0007272 GCST90281191 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Albumin levels 72,296 Korean ancestry individuals NA NR [8056211] (imputed) 49 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90255417 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Creatinine levels 72,297 Korean ancestry individuals NA NR [8056211] (imputed) 42 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90255418 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Aspartate aminotransferase levels 70,672 Korean ancestry individuals NA NR [8056211] (imputed) 45 aspartate aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004736 GCST90255419 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Total bilirubin levels 49,874 Korean ancestry individuals NA NR [8056211] (imputed) 72 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90255420 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Alanine aminotransferase levels 70,550 Korean ancestry individuals NA NR [8056211] (imputed) 26 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90255421 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Total cholesterol levels 72,297 Korean ancestry individuals NA NR [8056211] (imputed) 102 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90255422 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Gamma-glutamyl transpeptidase levels 67,467 Korean ancestry individuals NA NR [8056211] (imputed) 116 serum gamma-glutamyl transferase measurement http://www.ebi.ac.uk/efo/EFO_0004532 GCST90255423 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. HDL cholesterol levels 72,297 Korean ancestry individuals NA NR [8056211] (imputed) 198 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90255424 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. LDL cholesterol levels 72,132 Korean ancestry individuals NA NR [8056211] (imputed) 84 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90255425 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Triglyceride levels 72,195 Korean ancestry individuals NA NR [8056211] (imputed) 133 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90255426 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. White blood cell count 54,365 Korean ancestry individuals NA NR [8056211] (imputed) 47 leukocyte count http://www.ebi.ac.uk/efo/EFO_0004308 GCST90255427 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Red blood cell count 54,364 Korean ancestry individuals NA NR [8056211] (imputed) 107 erythrocyte count http://www.ebi.ac.uk/efo/EFO_0004305 GCST90255428 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hemoglobin levels 70,643 Korean ancestry individuals NA NR [8056211] (imputed) 46 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90255429 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Hematocrit levels 54,365 Korean ancestry individuals NA NR [8056211] (imputed) 34 hematocrit http://www.ebi.ac.uk/efo/EFO_0004348 GCST90255430 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Platelet count 53,929 Korean ancestry individuals NA NR [8056211] (imputed) 133 platelet count http://www.ebi.ac.uk/efo/EFO_0004309 GCST90255431 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Age at menarche 45,615 Korean ancestry individuals NA NR [8056211] (imputed) 4 age at menarche http://www.ebi.ac.uk/efo/EFO_0004703 GCST90255432 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Age at menopause 28,212 Korean ancestry individuals NA NR [8056211] (imputed) 5 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90255433 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Protein in urine 69,561 Korean ancestry individuals NA NR [8056211] (imputed) 0 urine protein measurement http://www.ebi.ac.uk/efo/EFO_0020074 GCST90255434 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Glucose in urine 69,545 Korean ancestry individuals NA NR [8056211] (imputed) 15 urine glucose measurement http://www.ebi.ac.uk/efo/EFO_0020075 GCST90255435 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Blood in urine 65,534 Korean ancestry individuals NA NR [8056211] (imputed) 16 urine blood measurement http://www.ebi.ac.uk/efo/EFO_0020076 GCST90255436 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Energy intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 energy intake measurement http://www.ebi.ac.uk/efo/EFO_0009374 GCST90255437 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Protein intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 protein intake measurement http://www.ebi.ac.uk/efo/EFO_0010810 GCST90255438 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Fat intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 fat intake measurement http://www.ebi.ac.uk/efo/EFO_0010809 GCST90255439 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Sugar intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 sugar consumption measurement http://www.ebi.ac.uk/efo/EFO_0010158 GCST90255440 Genome-wide genotyping array 2023-03-30 36777999 Nam K 2022-10-05 Cell Genom www.ncbi.nlm.nih.gov/pubmed/36777999 Genome-wide study on 72,298 individuals in Korean biobank data for 76 traits. Calcium intake 66,238 Korean ancestry individuals NA NR [8056211] (imputed) 0 calcium intake measurement http://www.ebi.ac.uk/efo/EFO_0006521 GCST90255441 Genome-wide genotyping array 2023-08-09 36176292 Zhang L 2022-09-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/36176292 A genome-wide association study identified one variant associated with static spatial working memory in Chinese population. Dynamic spatial working memory 439 Chinese ancestry individuals NA NR [4196499] (imputed) 0 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST90133163 Genome-wide genotyping array 2023-08-09 36176292 Zhang L 2022-09-13 Front Genet www.ncbi.nlm.nih.gov/pubmed/36176292 A genome-wide association study identified one variant associated with static spatial working memory in Chinese population. Static spatial working memory 432 Chinese ancestry individuals NA NR [4196499] (imputed) 1 short-term memory http://www.ebi.ac.uk/efo/EFO_0004335 GCST90133162 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Inflammatory bowel disease 16,421 European ancestry male cases, 16,780 European ancestry male controls NA Illumina [NR] 7 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90301317 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Inflammatory bowel disease 18,158 European ancestry female cases, 22,345 European ancestry female controls NA Illumina [NR] 29 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90301318 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Inflammatory bowel disease 34,579 European ancestry cases, 39,125 European ancestry controls NA Illumina [NR] 34 inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0003767 GCST90301319 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Inflammatory bowel disease x sex interaction (2df) 34,579 European ancestry cases, 39,125 European ancestry controls NA Illumina [NR] 36 sex interaction measurement, inflammatory bowel disease http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0003767 GCST90301320 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Ulcerative colitis 7,527 European ancestry male cases, 16,780 European ancestry male controls NA Illumina [NR] 5 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90301321 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Ulcerative colitis 7,196 European ancestry female cases, 22,345 European ancestry female controls NA Illumina [NR] 9 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90301322 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Ulcerative colitis 14,723 European ancestry cases, 39,125 European ancestry controls NA Illumina [NR] 13 ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0000729 GCST90301323 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Ulcerative colitis x sex interaction (2df) 14,723 European ancestry cases, 39,125 European ancestry controls NA Illumina [NR] 14 sex interaction measurement, ulcerative colitis http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0000729 GCST90301324 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Crohn's disease 8,653 European ancestry male cases, 16,780 European ancestry male controls NA Illumina [NR] 4 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90301325 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Crohn's disease 10,760 European ancestry female cases, 22,345 European ancestry female controls NA Illumina [NR] 22 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90301326 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Crohn's disease 19,413 European ancestry cases, 39,125 European ancestry controls NA Illumina [NR] 24 Crohn's disease http://www.ebi.ac.uk/efo/EFO_0000384 GCST90301327 Genome-wide genotyping array 2023-11-30 37262302 Khrom M 2023-06-01 Inflamm Bowel Dis www.ncbi.nlm.nih.gov/pubmed/37262302 Sex-Dimorphic Analyses Identify Novel and Sex-Specific Genetic Associations in Inflammatory Bowel Disease. Crohn's disease x sex interaction (2df) 19,413 European ancestry cases, 39,125 European ancestry controls NA Illumina [NR] 26 sex interaction measurement, Crohn's disease http://www.ebi.ac.uk/efo/EFO_0008343, http://www.ebi.ac.uk/efo/EFO_0000384 GCST90301328 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Alnus glutinosa 1) 52 Japanese ancestry pediatric cases, 512 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296334 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Alternaria alternata 1) 20 Japanese ancestry pediatric cases, 544 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296335 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Ambrosia artemisiifolia 1) 66 Japanese ancestry pediatric cases, 498 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 75 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296336 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Arachis hypogaea 8) 41 Japanese ancestry pediatric cases, 523 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296337 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Betula verrucosa 1) 84 Japanese ancestry pediatric cases, 480 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296338 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Betula verrucosa 2) 37 Japanese ancestry pediatric cases, 527 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296339 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Blomia tropicalis 5) 46 Japanese ancestry pediatric cases, 518 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296340 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Canis familiaris 1) 52 Japanese ancestry pediatric cases, 512 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296341 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Corylus avellana 1.0101) 59 Japanese ancestry pediatric cases, 505 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296342 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Corylus avellana 1.0401) 71 Japanese ancestry pediatric cases, 493 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296343 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Cryptomeria japonica 1) 327 Japanese ancestry pediatric cases, 237 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296344 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Cupressus arizonica 1) 261 Japanese ancestry pediatric cases, 303 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296345 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Cynodon dactylon 1) 81 Japanese ancestry pediatric cases, 483 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296346 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Dermatophagoides farinae 1) 316 Japanese ancestry pediatric cases, 248 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296347 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Dermatophagoides farinae 2) 280 Japanese ancestry pediatric cases, 284 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296348 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Dermatophagoides pteronyssinus 1) 295 Japanese ancestry pediatric cases, 269 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296349 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Dermatophagoides pteronyssinus 2) 276 Japanese ancestry pediatric cases, 288 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296350 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Felis domesticus 1) 156 Japanese ancestry pediatric cases, 408 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296351 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Felis domesticus 4) 19 Japanese ancestry pediatric cases, 545 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296352 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Glycine max 4) 36 Japanese ancestry pediatric cases, 528 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296353 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Hevea brasiliensis 8) 50 Japanese ancestry pediatric cases, 514 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 77 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296354 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Juglans regia 2) 43 Japanese ancestry pediatric cases, 521 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296355 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Lepidoglyphus destructor 2) 38 Japanese ancestry pediatric cases, 526 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296356 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Malus domestica 1) 70 Japanese ancestry pediatric cases, 494 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296357 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Mercurialis annua 1) 41 Japanese ancestry pediatric cases, 523 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 4 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296358 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Penaeus monodon 2) 17 Japanese ancestry pediatric cases, 547 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296359 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Phleum pratense 1) 62 Japanese ancestry pediatric cases, 502 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 1 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296360 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Phleum pratense 12) 25 Japanese ancestry pediatric cases, 539 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296361 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Phleum pratense 4) 60 Japanese ancestry pediatric cases, 504 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296362 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Phleum pratense 5) 41 Japanese ancestry pediatric cases, 523 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296363 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen component sensitization (Platanus acerifolia 2) 58 Japanese ancestry pediatric cases, 506 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296364 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (2S albumin) 22 Japanese ancestry pediatric cases, 542 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296365 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (7S globulin) 50 Japanese ancestry pediatric cases, 514 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296366 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Arginine kinase) 17 Japanese ancestry pediatric cases, 547 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296367 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Berberine bridge enzyme) 60 Japanese ancestry pediatric cases, 504 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296368 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Beta expansin) 93 Japanese ancestry pediatric cases, 471 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296369 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Cystein protease) 319 Japanese ancestry pediatric cases, 245 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296370 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Grass group 5) 41 Japanese ancestry pediatric cases, 523 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296371 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Lipocalin) 69 Japanese ancestry pediatric cases, 495 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296372 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Mite group 5/21) 46 Japanese ancestry pediatric cases, 518 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296373 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (NPC2 family) 280 Japanese ancestry pediatric cases, 284 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296374 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Pectate lyase) 333 Japanese ancestry pediatric cases, 231 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296375 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Polygalacturonase) 58 Japanese ancestry pediatric cases, 506 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296376 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (PR-10 Protein) 93 Japanese ancestry pediatric cases, 471 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296377 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Profilin) 50 Japanese ancestry pediatric cases, 514 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296378 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Tropomyosin) 18 Japanese ancestry pediatric cases, 546 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296379 Genome-wide genotyping array 2023-10-26 37780799 Morii W 2023-02-20 J Allergy Clin Immunol Glob www.ncbi.nlm.nih.gov/pubmed/37780799 A genome-wide association study for allergen component sensitizations identifies allergen component-specific and allergen protein group-specific associations. Allergen protein group sensitization (Uteroglobin) 156 Japanese ancestry pediatric cases, 408 Japanese ancestry pediatric controls NA Illumina [6471740] (imputed) 0 allergic sensitization measurement http://www.ebi.ac.uk/efo/EFO_0005298 GCST90296380 Genome-wide genotyping array 2023-11-01 37846649 Wei X 2023-10-17 Int J Cancer www.ncbi.nlm.nih.gov/pubmed/37846649 Development and evaluation of a polygenic risk score for lung cancer in never-smoking women: A large-scale prospective Chinese cohort study. Lung cancer in never smokers 8,595 East Asian ancestry female cases, 8,275 East Asian ancestry female controls NA NR [9452098] (imputed) 9 lung carcinoma http://www.ebi.ac.uk/efo/EFO_0001071 GCST90277434 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 475,645 European ancestry individuals, 8,590 African ancestry individuals, 85,279 East Asian ancestry individuals, 4,270 South Asian ancestry individuals, 14,668 Hispanic or Latin American individuals NA Affymetrix, Illumina [63380712] (imputed) 223 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90244092 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 475,645 European ancestry individuals, 8,590 African ancestry individuals, 85,279 East Asian ancestry individuals, 4,270 South Asian ancestry individuals, 14,668 Hispanic or Latin American individuals NA Affymetrix, Illumina [63372548] (imputed) 251 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90244093 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 475,645 European ancestry individuals, 8,590 African ancestry individuals, 85,279 East Asian ancestry individuals, 4,270 South Asian ancestry individuals, 14,668 Hispanic or Latin American individuals NA Affymetrix, Illumina [63372103] (imputed) 406 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90244094 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 393,161 European ancestry individuals, 4,227 African ancestry individuals, 1,564 East Asian ancestry individuals, 4,270 South Asian ancestry individuals, 2,798 Hispanic or Latin American individuals NA Affymetrix, Illumina [50317128] (imputed) 140 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90244095 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 475,645 European ancestry individuals NA Affymetrix, Illumina [53405509] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90292609 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 475,645 European ancestry individuals NA Affymetrix, Illumina [53394432] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90292610 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 475,645 European ancestry individuals NA Affymetrix, Illumina [53393865] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90292611 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 393,161 European ancestry individuals NA Affymetrix, Illumina [48526691] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90292612 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 154,989 European ancestry individuals NA Affymetrix, Illumina [30906205] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90292613 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 154,989 European ancestry individuals NA Affymetrix, Illumina [30857058] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90292614 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 154,989 European ancestry individuals NA Affymetrix, Illumina [30855467] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90292615 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 72,505 European ancestry individuals NA Affymetrix, Illumina [27123211] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90292616 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 320,656 European ancestry individuals NA Affymetrix, Illumina [51605650] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90292617 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 320,656 European ancestry individuals NA Affymetrix, Illumina [51602935] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90292618 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 320,656 European ancestry individuals NA Affymetrix, Illumina [51602372] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90292619 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 320,656 European ancestry individuals NA Affymetrix, Illumina [47402251] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90292620 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 4,227 African ancestry individuals NA Affymetrix, Illumina [19727083] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90292621 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 4,227 African ancestry individuals NA Affymetrix, Illumina [19727083] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90292622 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 4,227 African ancestry individuals NA Affymetrix, Illumina [19727083] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90292623 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 4,227 African ancestry individuals NA Affymetrix, Illumina [19726556] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90292624 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 4,270 South Asian ancestry individuals NA Affymetrix, Illumina [19756488] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90292625 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 4,270 South Asian ancestry individuals NA Affymetrix, Illumina [19756488] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90292626 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 4,270 South Asian ancestry individuals NA Affymetrix, Illumina [19756488] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90292627 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 4,270 South Asian ancestry individuals NA Affymetrix, Illumina [19754280] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90292628 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 1,564 East Asian ancestry individuals NA Affymetrix, Illumina [11445370] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90292629 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 1,564 East Asian ancestry individuals NA Affymetrix, Illumina [11445370] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90292630 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 1,564 East Asian ancestry individuals NA Affymetrix, Illumina [11445370] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90292631 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 1,564 East Asian ancestry individuals NA Affymetrix, Illumina [11445370] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90292632 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1) 2,798 Hispanic or Latin American individuals NA Affymetrix, Illumina [18545026] (imputed) 0 forced expiratory volume http://www.ebi.ac.uk/efo/EFO_0004314 GCST90292633 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (forced vital capacity) 2,798 Hispanic or Latin American individuals NA Affymetrix, Illumina [18545026] (imputed) 0 vital capacity http://www.ebi.ac.uk/efo/EFO_0004312 GCST90292634 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Lung function (FEV1/FVC) 2,798 Hispanic or Latin American individuals NA Affymetrix, Illumina [18545026] (imputed) 0 FEV/FEC ratio http://www.ebi.ac.uk/efo/EFO_0004713 GCST90292635 Genome-wide genotyping array 2023-12-12 36914875 Shrine N 2023-03-13 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36914875 Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. Peak expiratory flow 2,798 Hispanic or Latin American individuals NA Affymetrix, Illumina [18545022] (imputed) 0 peak expiratory flow http://www.ebi.ac.uk/efo/EFO_0009718 GCST90292636 Genome-wide genotyping array 2023-12-13 37359372 Nardone GG 2023-06-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/37359372 Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations. Color vision defects (Deutan-Protan) 31 Silk Road (founder/genetic isolate) cases, 483 Silk Road (founder/genetic isolate) controls NA Illumina [7783479] (imputed) 487 color vision disorder http://purl.obolibrary.org/obo/MONDO_0001703 GCST90301670 Genome-wide genotyping array 2023-12-12 37359372 Nardone GG 2023-06-09 Front Genet www.ncbi.nlm.nih.gov/pubmed/37359372 Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations. Color vision defects (Tritan) 12 Silk Road (founder/genetic isolate) cases, 508 Silk Road (founder/genetic isolate) controls NA Illumina [7783479] (imputed) 883 color vision disorder http://purl.obolibrary.org/obo/MONDO_0001703 GCST90301671 Genome-wide genotyping array 2023-12-13 38029837 Deecke L 2023-11-27 J Invest Dermatol www.ncbi.nlm.nih.gov/pubmed/38029837 Variants in the TERT gene increase the occurrence of solar lentigines by modifying telomerase expression exclusively in the skin. Solar lentigines (non-facial) 1,137 German ancestry elderly individuals NA Affymetrix [7171623] (imputed) 18 solar lentigines measurement http://www.ebi.ac.uk/efo/EFO_0007850 GCST90281274 Genome-wide genotyping array 2023-11-30 37264206 Kachuri L 2023-06-01 Nat Med www.ncbi.nlm.nih.gov/pubmed/37264206 Genetically adjusted PSA levels for prostate cancer screening. Prostate-specific antigen levels 85,824 European ancestry individuals, 3,509 African American or Afro-Caribbean individuals, 3,337 East Asian ancestry individuals, 3,098 Hispanic or Latin American individuals NA Illumina [NR] (imputed) 128 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST90301330 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum fractional anisotropy (MOSTest) 31,727 British ancestry individuals NA NR [NR] (imputed) 41 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90281340 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum fractional anisotropy (genu) 31,727 British ancestry individuals NA NR [NR] (imputed) 21 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90281341 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum fractional anisotropy (body) 31,727 British ancestry individuals NA NR [NR] (imputed) 21 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90281342 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum fractional anisotropy (splenium) 31,727 British ancestry individuals NA NR [NR] (imputed) 21 mean fractional anisotropy measurement http://www.ebi.ac.uk/efo/EFO_0008399 GCST90281343 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum anterior volume 33,861 British ancestry individuals NA NR [NR] (imputed) 20 corpus callosum anterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010295 GCST90281344 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum mid-anterior volume 33,861 British ancestry individuals NA NR [NR] (imputed) 15 corpus callosum mid-anterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010297 GCST90281345 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum central volume 33,861 British ancestry individuals NA NR [NR] (imputed) 13 corpus callosum central volume measurement http://www.ebi.ac.uk/efo/EFO_0010296 GCST90281346 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum Mid-posterior volume 33,861 British ancestry individuals NA NR [NR] (imputed) 12 corpus collosum mid-posterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010300 GCST90281347 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum posterior volume 33,861 British ancestry individuals NA NR [NR] (imputed) 36 corpus callosum posterior volume measurement http://www.ebi.ac.uk/efo/EFO_0010298 GCST90281348 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum volume 33,861 British ancestry individuals NA NR [NR] (imputed) 38 corpus callosum volume measurement http://www.ebi.ac.uk/efo/EFO_0010299 GCST90281349 Genome-wide genotyping array 2023-09-21 37164063 Chen SJ 2023-05-08 J Affect Disord www.ncbi.nlm.nih.gov/pubmed/37164063 The genetic architecture of the corpus callosum and its genetic overlap with common neuropsychiatric diseases. Corpus callosum volume (MOSTest) 33,861 British ancestry individuals NA NR [NR] (imputed) 63 corpus callosum volume measurement http://www.ebi.ac.uk/efo/EFO_0010299 GCST90281350 Genome-wide genotyping array 2023-09-07 36927824 Bovonratwet P 2023-03-16 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/36927824 Identification of Novel Genetic Markers for the Risk of Spinal Pathologies: A Genome-Wide Association Study of 2 Biobanks. Lumbar spondylolisthesis 1,964 European ancestry cases, 387,449 European ancestry controls NA NR [784256] 3 spondylolisthesis http://www.ebi.ac.uk/efo/EFO_0007493 GCST90281185 Genome-wide genotyping array 2023-09-07 36927824 Bovonratwet P 2023-03-16 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/36927824 Identification of Novel Genetic Markers for the Risk of Spinal Pathologies: A Genome-Wide Association Study of 2 Biobanks. Spinal stenosis 6,944 European ancestry cases, 382,469 European ancestry controls 11,291 European ancestry cases, 194,289 European ancestry controls NR [784256] 1 spinal stenosis http://www.ebi.ac.uk/efo/EFO_0007490 GCST90281186 Genome-wide genotyping array 2023-09-07 36927824 Bovonratwet P 2023-03-16 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/36927824 Identification of Novel Genetic Markers for the Risk of Spinal Pathologies: A Genome-Wide Association Study of 2 Biobanks. Degenerative disc disease 11,310 European ancestry cases, 378,103 European ancestry controls 24,239 European ancestry cases, 194,289 European ancestry controls NR [784256] 4 lumbar disc degeneration http://www.ebi.ac.uk/efo/EFO_0004994 GCST90281187 Genome-wide genotyping array 2023-09-07 36927824 Bovonratwet P 2023-03-16 J Bone Joint Surg Am www.ncbi.nlm.nih.gov/pubmed/36927824 Identification of Novel Genetic Markers for the Risk of Spinal Pathologies: A Genome-Wide Association Study of 2 Biobanks. Pseudarthrosis after spinal fusion 259 European ancestry cases, 389,154 European ancestry controls NA NR [784256] 4 fractures, ununited http://www.ebi.ac.uk/efo/EFO_0009707 GCST90281188 Genome-wide genotyping array 2023-09-21 37398645 Huang YX 2023-06-16 Front Immunol www.ncbi.nlm.nih.gov/pubmed/37398645 A shared genetic contribution to osteoarthritis and COVID-19 outcomes: a large-scale genome-wide cross-trait analysis. Critical COVID-19 or osteoarthritis (MTAG) 314,870 European ancestry individuals with osteoarthritis data, 1,388,342 European ancestry individuals with critical COVID-19 data NA NR [NR] 11 COVID-19, osteoarthritis http://purl.obolibrary.org/obo/MONDO_0100096, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90292530 Genome-wide genotyping array 2023-09-21 37398645 Huang YX 2023-06-16 Front Immunol www.ncbi.nlm.nih.gov/pubmed/37398645 A shared genetic contribution to osteoarthritis and COVID-19 outcomes: a large-scale genome-wide cross-trait analysis. COVID-19 hospitalization or osteoarthritis (MTAG) 314,870 European ancestry individuals with osteoarthritis data, 1,887,658 European ancestry individuals with COVID-19 hospitalization data NA NR [NR] 9 COVID-19, osteoarthritis http://purl.obolibrary.org/obo/MONDO_0100096, http://purl.obolibrary.org/obo/MONDO_0005178 GCST90292531 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Platelet side scatter 29,675 European ancestry individuals NA Affymetrix [29500000] (imputed) 54 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90281192 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Platelet side fluorescence 29,678 European ancestry individuals NA Affymetrix [29500000] (imputed) 72 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90281193 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Platelet forward scatter 29,662 European ancestry individuals NA Affymetrix [29500000] (imputed) 59 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90281194 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Platelet side scatter distribution width 29,658 European ancestry individuals NA Affymetrix [29500000] (imputed) 46 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90281195 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Platelet side fluorescence distribution width 29,552 European ancestry individuals NA Affymetrix [29500000] (imputed) 58 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90281196 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Platelet forward scatter distribution width 29,618 European ancestry individuals NA Affymetrix [29500000] (imputed) 48 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90281197 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. High fluorescence immature platelet fraction 36,829 European ancestry individuals NA Affymetrix [29500000] (imputed) 103 immature platelet measurement http://www.ebi.ac.uk/efo/EFO_0803541 GCST90281198 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Immature platelet count 36,618 European ancestry individuals NA Affymetrix [29500000] (imputed) 89 immature platelet count http://www.ebi.ac.uk/efo/EFO_0803544 GCST90281199 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Immature platelet fraction 36,615 European ancestry individuals NA Affymetrix [29500000] (imputed) 98 immature platelet fraction http://www.ebi.ac.uk/efo/EFO_0009187 GCST90281200 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Platelet large cell ratio 37,935 European ancestry individuals NA Affymetrix [29500000] (imputed) 90 platelet measurement http://www.ebi.ac.uk/efo/EFO_0005036 GCST90281201 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Red blood cell side scatter 30,528 European ancestry individuals NA Affymetrix [29500000] (imputed) 28 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281202 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Red blood cell side fluorescence 30,551 European ancestry individuals NA Affymetrix [29500000] (imputed) 39 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281203 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Red blood cell forward scatter 38,005 European ancestry individuals NA Affymetrix [29500000] (imputed) 54 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281204 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Red blood cell side fluorescence distribution width 30,565 European ancestry individuals NA Affymetrix [29500000] (imputed) 13 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281205 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Red blood cell forward scatter distribution width 30,417 European ancestry individuals NA Affymetrix [29500000] (imputed) 12 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281206 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Hyper-haemoglobinised percentage of red cells 38,553 European ancestry individuals NA Affymetrix [29500000] (imputed) 39 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90281207 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Macrocytic percentage of red cells 37,432 European ancestry individuals NA Affymetrix [29500000] (imputed) 16 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281208 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Microcytic percentage of red cells 39,184 European ancestry individuals NA Affymetrix [29500000] (imputed) 47 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281209 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Red blood cell haemoglobin equivalent 38,200 European ancestry individuals NA Affymetrix [29500000] (imputed) 54 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90281210 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Red cell distribution width - standard deviation 39,313 European ancestry individuals NA Affymetrix [29500000] (imputed) 43 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281211 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Reticulocyte side fluorescence 30,485 European ancestry individuals NA Affymetrix [29500000] (imputed) 35 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281212 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Reticulocyte forward scatter 38,277 European ancestry individuals NA Affymetrix [29500000] (imputed) 52 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281213 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. High fluorescent percentage of reticulocytes 37,931 European ancestry individuals NA Affymetrix [29500000] (imputed) 27 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281214 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Medium fluorescent percentage of reticulocytes 39,459 European ancestry individuals NA Affymetrix [29500000] (imputed) 43 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281215 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Low fluorescent percentage of reticulocytes 39,470 European ancestry individuals NA Affymetrix [29500000] (imputed) 48 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281216 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Reticulocyte haemoglobin equivalent 39,127 European ancestry individuals NA Affymetrix [29500000] (imputed) 53 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90281217 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Immature reticulocyte forward scatter 38,711 European ancestry individuals NA Affymetrix [29500000] (imputed) 30 immature reticulocyte measurement http://www.ebi.ac.uk/efo/EFO_0803545 GCST90281218 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Delta of the haemoglobin equivalents 38,798 European ancestry individuals NA Affymetrix [29500000] (imputed) 5 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90281219 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Delta of the red cell haemoglobins 30,298 European ancestry individuals NA Affymetrix [29500000] (imputed) 9 hemoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004509 GCST90281220 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Reticulocyte production index 39,566 European ancestry individuals NA Affymetrix [29500000] (imputed) 38 erythrocyte measurement http://www.ebi.ac.uk/efo/EFO_0005047 GCST90281221 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Neutrophil side scatter 38,341 European ancestry individuals NA Affymetrix [29500000] (imputed) 72 neutrophil measurement http://www.ebi.ac.uk/efo/EFO_0803548 GCST90281222 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Neutrophil side fluorescence 38,336 European ancestry individuals NA Affymetrix [29500000] (imputed) 73 neutrophil measurement http://www.ebi.ac.uk/efo/EFO_0803548 GCST90281223 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Neutrophil forward scatter 38,084 European ancestry individuals NA Affymetrix [29500000] (imputed) 70 neutrophil measurement http://www.ebi.ac.uk/efo/EFO_0803548 GCST90281224 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Neutrophil side scatter distribution width 39,596 European ancestry individuals NA Affymetrix [29500000] (imputed) 20 neutrophil measurement http://www.ebi.ac.uk/efo/EFO_0803548 GCST90281225 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Neutrophil side fluorescence distribution width 39,004 European ancestry individuals NA Affymetrix [29500000] (imputed) 19 neutrophil measurement http://www.ebi.ac.uk/efo/EFO_0803548 GCST90281226 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Neutrophil forward scatter distribution width 39,656 European ancestry individuals NA Affymetrix [29500000] (imputed) 14 neutrophil measurement http://www.ebi.ac.uk/efo/EFO_0803548 GCST90281227 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Immature granulocyte count 37,939 European ancestry individuals NA Affymetrix [29500000] (imputed) 13 immature granulocyte count http://www.ebi.ac.uk/efo/EFO_0803542 GCST90281228 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Immature granulocyte percentage of white cells 37,926 European ancestry individuals NA Affymetrix [29500000] (imputed) 7 immature granulocyte measurement http://www.ebi.ac.uk/efo/EFO_0803543 GCST90281229 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Eosinophil side scatter 30,328 European ancestry individuals NA Affymetrix [29500000] (imputed) 51 eosinophil measurement http://www.ebi.ac.uk/efo/EFO_0803540 GCST90281230 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Eosinophil side fluorescence 30,531 European ancestry individuals NA Affymetrix [29500000] (imputed) 41 eosinophil measurement http://www.ebi.ac.uk/efo/EFO_0803540 GCST90281231 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Eosinophil forward scatter 30,352 European ancestry individuals NA Affymetrix [29500000] (imputed) 28 eosinophil measurement http://www.ebi.ac.uk/efo/EFO_0803540 GCST90281232 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Eosinophil side scatter distribution width 29,325 European ancestry individuals NA Affymetrix [29500000] (imputed) 16 eosinophil measurement http://www.ebi.ac.uk/efo/EFO_0803540 GCST90281233 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Eosinophil side fluorescence distribution width 30,284 European ancestry individuals NA Affymetrix [29500000] (imputed) 5 eosinophil measurement http://www.ebi.ac.uk/efo/EFO_0803540 GCST90281234 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Eosinophil forward scatter distribution width 29,084 European ancestry individuals NA Affymetrix [29500000] (imputed) 12 eosinophil measurement http://www.ebi.ac.uk/efo/EFO_0803540 GCST90281235 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Basophil side fluorescence 30,327 European ancestry individuals NA Affymetrix [29500000] (imputed) 20 basophil measurement http://www.ebi.ac.uk/efo/EFO_0803539 GCST90281236 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Basophil forward scatter 30,614 European ancestry individuals NA Affymetrix [29500000] (imputed) 8 basophil measurement http://www.ebi.ac.uk/efo/EFO_0803539 GCST90281237 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Basophil side fluorescence distribution width 29,720 European ancestry individuals NA Affymetrix [29500000] (imputed) 20 basophil measurement http://www.ebi.ac.uk/efo/EFO_0803539 GCST90281238 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Basophil forward scatter distribution width 30,601 European ancestry individuals NA Affymetrix [29500000] (imputed) 26 basophil measurement http://www.ebi.ac.uk/efo/EFO_0803539 GCST90281239 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Monocyte side scatter 39,608 European ancestry individuals NA Affymetrix [29500000] (imputed) 28 monocyte measurement http://www.ebi.ac.uk/efo/EFO_0803547 GCST90281240 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Monocyte side fluorescence 39,586 European ancestry individuals NA Affymetrix [29500000] (imputed) 39 monocyte measurement http://www.ebi.ac.uk/efo/EFO_0803547 GCST90281241 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Epilepsy 27,559 European ancestry cases, 42,436 European ancestry controls, 1,626 African ancestry cases, 3,680 African ancestry controls, 759 Asian ancestry cases, 6,422 Asian ancestry controls NA Illumina [4900000] (imputed) 6 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90271608 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Genetic generalized epilepsy 6,952 European ancestry cases, 42,436 European ancestry controls, 118 African ancestry cases, 3,680 African ancestry controls, 337 Asian ancestry cases, 6,422 Asian ancestry controls NA Illumina [4900000] (imputed) 36 generalised epilepsy http://www.ebi.ac.uk/efo/EFO_0005917 GCST90271609 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Focal epilepsy 14,939 European ancestry cases, 42,436 European ancestry controls, 1,129 African ancestry cases, 3,680 African ancestry controls, 316 Asian ancestry cases, 6,422 Asian ancestry controls NA Illumina [4900000] (imputed) 0 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90271610 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Epilepsy 27,559 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 0 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90271611 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Genetic generalized epilepsy 6,952 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 0 generalised epilepsy http://www.ebi.ac.uk/efo/EFO_0005917 GCST90271612 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Focal epilepsy 14,939 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 0 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90271613 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Juvenile myoclonic epilepsy 1,732 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 3 juvenile myoclonic epilepsy http://purl.obolibrary.org/obo/MONDO_0009696 GCST90271614 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Juvenile absence epilepsy 662 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 0 juvenile absence epilepsy http://purl.obolibrary.org/obo/MONDO_0011876 GCST90271615 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Childhood absence epilepsy 1,049 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 2 childhood absence epilepsy http://purl.obolibrary.org/obo/MONDO_0010826 GCST90271616 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Epilepsy (generalized, with tonic-clonic seizures alone) 485 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 0 epilepsy with generalized tonic-clonic seizures http://www.ebi.ac.uk/efo/EFO_0007262 GCST90271617 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Focal epilepsy (with hippocampal sclerosis) 1,260 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 1 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90271618 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Focal epilepsy (lesion negative) 5,778 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 0 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90271619 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Focal epilepsy (with lesion other than hippocampal sclerosis) 4,213 European ancestry cases, 42,436 European ancestry controls NA Illumina [4900000] (imputed) 0 partial epilepsy http://www.ebi.ac.uk/efo/EFO_0004263 GCST90271620 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Genetic generalized epilepsy or focal epilepsy (pleiotropy) 6,952 European ancestry genetic generalized epilepsy cases, 14,939 European ancestry focal epilepsy cases, 42,434 European ancestry controls NA Illumina [NR] (imputed) 4 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90281287 Genome-wide genotyping array 2023-09-19 37653029 International League Against Epilepsy Consortium on Complex Epilepsies 2023-08-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/37653029 GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture. Epilepsy 13,889 European ancestry female cases, 19,676 European ancestry female controls NA Illumina [NR] (imputed) 1 epilepsy http://www.ebi.ac.uk/efo/EFO_0000474 GCST90281291 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Monocyte forward scatter 39,460 European ancestry individuals NA Affymetrix [29500000] (imputed) 8 monocyte measurement http://www.ebi.ac.uk/efo/EFO_0803547 GCST90281242 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Monocyte side scatter distribution width 39,417 European ancestry individuals NA Affymetrix [29500000] (imputed) 5 monocyte measurement http://www.ebi.ac.uk/efo/EFO_0803547 GCST90281243 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Monocyte side fluorescence distribution width 39,631 European ancestry individuals NA Affymetrix [29500000] (imputed) 13 monocyte measurement http://www.ebi.ac.uk/efo/EFO_0803547 GCST90281244 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Monocyte forward scatter distribution width 39,650 European ancestry individuals NA Affymetrix [29500000] (imputed) 5 monocyte measurement http://www.ebi.ac.uk/efo/EFO_0803547 GCST90281245 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Lymphocyte side scatter 39,646 European ancestry individuals NA Affymetrix [29500000] (imputed) 35 lymphocyte measurement http://www.ebi.ac.uk/efo/EFO_0803546 GCST90281246 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Lymphocyte side fluorescence 39,640 European ancestry individuals NA Affymetrix [29500000] (imputed) 33 lymphocyte measurement http://www.ebi.ac.uk/efo/EFO_0803546 GCST90281247 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Lymphocyte forward scatter 38,877 European ancestry individuals NA Affymetrix [29500000] (imputed) 12 lymphocyte measurement http://www.ebi.ac.uk/efo/EFO_0803546 GCST90281248 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Lymphocyte side scatter distribution width 39,654 European ancestry individuals NA Affymetrix [29500000] (imputed) 11 lymphocyte measurement http://www.ebi.ac.uk/efo/EFO_0803546 GCST90281249 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Lymphocyte side fluorescence distribution width 39,647 European ancestry individuals NA Affymetrix [29500000] (imputed) 12 lymphocyte measurement http://www.ebi.ac.uk/efo/EFO_0803546 GCST90281250 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Lymphocyte forward scatter distribution width 39,571 European ancestry individuals NA Affymetrix [29500000] (imputed) 4 lymphocyte measurement http://www.ebi.ac.uk/efo/EFO_0803546 GCST90281251 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Reactive lymphocyte count 30,589 European ancestry individuals NA Affymetrix [29500000] (imputed) 17 lymphocyte count http://www.ebi.ac.uk/efo/EFO_0004587 GCST90281252 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Reactive percentage of lymphocytes 30,240 European ancestry individuals NA Affymetrix [29500000] (imputed) 15 lymphocyte measurement http://www.ebi.ac.uk/efo/EFO_0803546 GCST90281253 Genome-wide genotyping array 2023-10-25 37596262 Akbari P 2023-08-18 Nat Commun www.ncbi.nlm.nih.gov/pubmed/37596262 A genome-wide association study of blood cell morphology identifies cellular proteins implicated in disease aetiology. Reactive lymphocyte percentage of white cells 30,577 European ancestry individuals NA Affymetrix [29500000] (imputed) 14 lymphocyte percentage of leukocytes http://www.ebi.ac.uk/efo/EFO_0007993 GCST90281254 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder 296,989 European ancestry individuals, 80,764 African American individuals, 31,877 Hispanic American individuals NA Affymetrix [NR] (imputed) 26 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90301659 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder 296,989 European ancestry individuals NA Affymetrix [11800000] (imputed) 15 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90301660 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder 80,764 African American individuals NA Affymetrix [19500000] (imputed) 3 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90301661 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder 31,877 Hispanic American individuals NA Affymetrix [8800000] (imputed) 1 alcohol use disorder measurement http://www.ebi.ac.uk/efo/EFO_0009458 GCST90301662 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder (consumption score) 296,989 European ancestry individuals, 80,764 African American individuals, 31,877 Hispanic American individuals NA Affymetrix [NR] (imputed) 24 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90301663 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder (consumption score) 296,989 European ancestry individuals NA Affymetrix [11800000] (imputed) 14 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90301664 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder (consumption score) 80,764 African American individuals NA Affymetrix [19500000] (imputed) 2 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90301665 Genome-wide genotyping array 2023-12-12 37282553 Kember RL 2023-06-07 Am J Psychiatry www.ncbi.nlm.nih.gov/pubmed/37282553 Genetic Underpinnings of the Transition From Alcohol Consumption to Alcohol Use Disorder: Shared and Unique Genetic Architectures in a Cross-Ancestry Sample. Alcohol use disorder (consumption score) 31,877 Hispanic American individuals NA Affymetrix [8800000] (imputed) 2 alcohol consumption measurement http://www.ebi.ac.uk/efo/EFO_0007878 GCST90301666 Genome-wide genotyping array 2023-10-26 35332129 Skuladottir AT 2022-03-24 Nat Commun www.ncbi.nlm.nih.gov/pubmed/35332129 A genome-wide meta-analysis identifies 50 genetic loci associated with carpal tunnel syndrome. Carpal tunnel syndrome 48,843 European ancestry cases, 1,190,837 European ancestry controls NA Affymetrix, Illumina [37071338] (imputed) 50 carpal tunnel syndrome http://www.ebi.ac.uk/efo/EFO_0004143 GCST90104786 Genome-wide genotyping array, Genome-wide sequencing 2023-10-27 37156489 Ahlstrom SE 2023-05-08 Acta Anaesthesiol Scand www.ncbi.nlm.nih.gov/pubmed/37156489 Clinical and genetic factors associated with post-operative nausea and vomiting after propofol anaesthesia. Post-operative nausea and vomiting in breast cancer surgery 187 Finnish ancestry female cases, 628 Finnish ancestry female controls NA Illumina [653034] 6 post operative nausea and vomiting http://www.ebi.ac.uk/efo/EFO_0004888 GCST90296446 Genome-wide genotyping array 2023-10-27 37805635 Park KW 2023-10-07 NPJ Parkinsons Dis www.ncbi.nlm.nih.gov/pubmed/37805635 Ethnicity- and sex-specific genome wide association study on Parkinson's disease. Parkinson's disease 1,050 East Asian ancestry cases, 5,000 East Asian ancestry controls NA Affymetrix [492970] 5 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90278092 Targeted genotyping array [K-CHIP] 2023-10-27 37805635 Park KW 2023-10-07 NPJ Parkinsons Dis www.ncbi.nlm.nih.gov/pubmed/37805635 Ethnicity- and sex-specific genome wide association study on Parkinson's disease. Parkinson's disease 554 East Asian ancestry female cases, 2,610 East Asian ancestry female controls NA Affymetrix [486510] 2 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90296432 Targeted genotyping array [K-CHIP] 2023-10-27 37805635 Park KW 2023-10-07 NPJ Parkinsons Dis www.ncbi.nlm.nih.gov/pubmed/37805635 Ethnicity- and sex-specific genome wide association study on Parkinson's disease. Parkinson's disease 496 East Asian ancestry male cases, 2,390 East Asian ancestry male controls NA Affymetrix [488631] 6 Parkinson disease http://purl.obolibrary.org/obo/MONDO_0005180 GCST90296433 Targeted genotyping array [K-CHIP] 2022-07-01 35361970 Okbay A 2022-03-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35361970 Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Educational attainment 3,037,499 European ancestry individuals NA Illumina [10675380] (imputed) 4829 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90105038 Genome-wide genotyping array 2022-07-01 35361970 Okbay A 2022-03-31 Nat Genet www.ncbi.nlm.nih.gov/pubmed/35361970 Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals. Educational attainment 2,713,033 European or unknown ancestry individuals NA Illumina [211581] (imputed) 57 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90105039 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Breast cancer or COVID-19 infection (pleiotropy) 133,384 European ancestry breast cancer cases, 122,616 European ancestry COVID-19 cases, 2,589,029 European ancestry controls NA NR [NR] 7 breast cancer, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007254, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296487 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Breast cancer or hospitalized COVID-19 (pleiotropy) 133,384 European ancestry breast cancer cases, 32,519 European ancestry hospitalized COVID-19 cases, 2,176,594 European ancestry controls NA NR [NR] 7 breast cancer, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007254, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296488 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Breast cancer or critical COVID-19 (pleiotropy) 133,384 European ancestry breast cancer cases, 13,769 European ancestry critical COVID-19 cases, 1,186,231 European ancestry controls NA NR [NR] 6 breast cancer, COVID-19 http://purl.obolibrary.org/obo/MONDO_0007254, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296489 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Ovarian cancer or COVID-19 infection (pleiotropy) 22,406 European ancestry ovarian cancer cases, 122,616 European ancestry COVID-19 cases, 2,516,181 European ancestry controls NA NR [NR] 5 ovarian carcinoma, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001075, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296490 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Ovarian cancer or hospitalized COVID-19 (pleiotropy) 22,406 European ancestry ovarian cancer cases, 32,519 European ancestry hospitalized COVID-19 cases, 2,103,746 European ancestry controls NA NR [NR] 6 ovarian carcinoma, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001075, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296491 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Ovarian cancer or critical COVID-19 (pleiotropy) 22,406 European ancestry ovarian cancer cases, 13,769 European ancestry critical COVID-19 cases, 1,113,383 European ancestry controls NA NR [NR] 4 ovarian carcinoma, COVID-19 http://www.ebi.ac.uk/efo/EFO_0001075, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296492 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Endometrial cancer or COVID-19 infection (pleiotropy) 12,906 European ancestry endometrial cancer cases, 122,616 European ancestry COVID-19 cases, 2,584,219 European ancestry controls NA NR [NR] 2 endometrial cancer, COVID-19 http://purl.obolibrary.org/obo/MONDO_0011962, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296493 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Endometrial cancer or hospitalized COVID-19 (pleiotropy) 12,906 European ancestry endometrial cancer cases, 32,519 European ancestry hospitalized COVID-19 cases, 2,171,784 European ancestry controls NA NR [NR] 3 endometrial cancer, COVID-19 http://purl.obolibrary.org/obo/MONDO_0011962, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296494 Genome-wide genotyping array 2023-10-30 37636041 Zhao X 2023-07-29 iScience www.ncbi.nlm.nih.gov/pubmed/37636041 A large-scale genome-wide cross-trait analysis for the effect of COVID-19 on female-specific cancers. Endometrial cancer or critical COVID-19 (pleiotropy) 12,906 European ancestry endometrial cancer cases, 13,769 European ancestry critical COVID-19 cases, 1,181,421 European ancestry controls NA NR [NR] 2 endometrial cancer, COVID-19 http://purl.obolibrary.org/obo/MONDO_0011962, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296495 Genome-wide genotyping array 2023-10-31 37572794 Glessner JT 2023-08-10 J Hepatol www.ncbi.nlm.nih.gov/pubmed/37572794 Biliary atresia is associated with polygenic susceptibility in ciliogenesis and planar polarity effector genes. Biliary atresia 811 European ancestry cases, 4,654 European ancestry controls NA Illumina [8534063] (imputed) 32 biliary atresia http://purl.obolibrary.org/obo/MONDO_0008867 GCST90296484 Genome-wide genotyping array 2023-10-27 37426090 Li Z 2023-06-23 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/37426090 Shared genetics and causal relationships between major depressive disorder and COVID-19 related traits: a large-scale genome-wide cross-trait meta-analysis. Major depressive disorder or severe COVID-19 (pleiotropy) 65,075 European ancestry MDD cases, 8,779 European ancestry severe COVID-19 cases, 1,234,427 European ancestry controls NA NR [NR] 7 major depressive disorder, COVID-19 http://purl.obolibrary.org/obo/MONDO_0002009, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296443 Genome-wide genotyping array 2023-10-27 37426090 Li Z 2023-06-23 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/37426090 Shared genetics and causal relationships between major depressive disorder and COVID-19 related traits: a large-scale genome-wide cross-trait meta-analysis. Major depressive disorder or hospitalized COVID-19 (pleiotropy) 65,075 European ancestry MDD cases, 24,274 European ancestry hospitalized COVID-19 cases, 2,294,081 European ancestry controls NA NR [NR] 6 major depressive disorder, COVID-19 http://purl.obolibrary.org/obo/MONDO_0002009, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296444 Genome-wide genotyping array 2023-10-27 37426090 Li Z 2023-06-23 Front Psychiatry www.ncbi.nlm.nih.gov/pubmed/37426090 Shared genetics and causal relationships between major depressive disorder and COVID-19 related traits: a large-scale genome-wide cross-trait meta-analysis. Major depressive disorder or COVID-19 infection (pleiotropy) 65,075 European ancestry MDD cases, 112,612 European ancestry COVID-19 infection cases, 2,706,631 European ancestry controls NA NR [NR] 5 major depressive disorder, COVID-19 http://purl.obolibrary.org/obo/MONDO_0002009, http://purl.obolibrary.org/obo/MONDO_0100096 GCST90296445 Genome-wide genotyping array 2023-09-19 37326842 Oberg Sysojev A 2023-06-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/37326842 Genome-wide investigation of persistence to treatment with methotrexate in early rheumatoid arthritis. Persistence with methotrexate treatment at one year in early rheumatoid arthritis 2,112 Swedish ancestry cases, 1,148 Swedish ancestry controls NA Illumina [5978812] (imputed) 9 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST90281046 Genome-wide genotyping array 2023-09-19 37326842 Oberg Sysojev A 2023-06-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/37326842 Genome-wide investigation of persistence to treatment with methotrexate in early rheumatoid arthritis. Persistence with methotrexate treatment at three years in early rheumatoid arthritis 1,412 Swedish ancestry cases, 1,810 Swedish ancestry controls NA Illumina [5978812] (imputed) 7 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST90281047 Genome-wide genotyping array 2023-09-19 37326842 Oberg Sysojev A 2023-06-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/37326842 Genome-wide investigation of persistence to treatment with methotrexate in early rheumatoid arthritis. Persistence with methotrexate treatment at one year in early seropositive rheumatoid arthritis 1,450 Swedish ancestry cases, 829 Swedish ancestry controls NA Illumina [5975193] (imputed) 0 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST90281048 Genome-wide genotyping array 2023-09-19 37326842 Oberg Sysojev A 2023-06-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/37326842 Genome-wide investigation of persistence to treatment with methotrexate in early rheumatoid arthritis. Persistence with methotrexate treatment at three years in early seropositive rheumatoid arthritis 953 Swedish ancestry cases, 1,300 Swedish ancestry controls NA Illumina [5975193] (imputed) 0 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST90281049 Genome-wide genotyping array 2023-09-19 37326842 Oberg Sysojev A 2023-06-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/37326842 Genome-wide investigation of persistence to treatment with methotrexate in early rheumatoid arthritis. Persistence with methotrexate treatment at one year in early seronegative rheumatoid arthritis 430 Swedish ancestry cases, 235 Swedish ancestry controls NA Illumina [5969557] (imputed) 0 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST90281050 Genome-wide genotyping array 2023-09-19 37326842 Oberg Sysojev A 2023-06-16 Rheumatology (Oxford) www.ncbi.nlm.nih.gov/pubmed/37326842 Genome-wide investigation of persistence to treatment with methotrexate in early rheumatoid arthritis. Persistence with methotrexate treatment at three years in early seronegative rheumatoid arthritis 303 Swedish ancestry cases, 355 Swedish ancestry controls NA Illumina [5969557] (imputed) 0 response to methotrexate http://purl.obolibrary.org/obo/GO_0031427 GCST90281051 Genome-wide genotyping array 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty 33,308 European ancestry cases, 74,199 European ancestry controls NA Illumina [3111172] 4 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245766 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing aid use 4,649 European ancestry cases, 74,199 European ancestry controls NA Illumina [2525780] 4 able to hear with hearing aids http://www.ebi.ac.uk/efo/EFO_0009720 GCST90245765 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty with background noise 49,339 European ancestry cases, 74,199 European ancestry controls NA Illumina [3412816] 3 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245767 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty and hearing difficulty with background noise 27,934 European ancestry cases, 74,199 European ancestry controls NA Illumina [3006650] 6 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245768 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing aid use 1,787 European ancestry cases, 22,402 European ancestry controls NA Illumina [1111966] 0 able to hear with hearing aids http://www.ebi.ac.uk/efo/EFO_0009720 GCST90245769 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty 12,194 European ancestry cases, 22,402 European ancestry controls NA Illumina [1422537] 3 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245770 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty with background noise 16,321 European ancestry cases, 22,402 European ancestry controls NA Illumina [1538800] 2 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245771 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty and hearing difficulty with background noise 10,476 European ancestry cases, 22,402 European ancestry controls NA Illumina [1372865] 3 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245772 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing aid use 6,436 European ancestry cases, 96,601 European ancestry controls NA Illumina [3029153] 12 able to hear with hearing aids http://www.ebi.ac.uk/efo/EFO_0009720 GCST90245773 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty 45,502 European ancestry cases, 96,601 European ancestry controls NA Illumina [3732745] 21 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245774 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty with background noise 65,660 European ancestry cases, 96,601 European ancestry controls NA Illumina [4062971] 7 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245775 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty and hearing difficulty with background noise 38,410 European ancestry cases, 96,601 European ancestry controls NA Illumina [3611725] 16 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245776 Exome genotyping array, Exome-wide sequencing 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing aid use 9,165 European ancestry cases, 141,007 European ancestry controls NA Affymetrix [50585965] (imputed) 0 able to hear with hearing aids http://www.ebi.ac.uk/efo/EFO_0009720 GCST90245777 Genome-wide genotyping array 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty 64,953 European ancestry cases, 141,007 European ancestry controls NA Affymetrix [52133404] (imputed) 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245778 Genome-wide genotyping array 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty with background noise 95,794 European ancestry cases, 141,007 European ancestry controls NA Affymetrix [52892564] (imputed) 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245779 Genome-wide genotyping array 2023-11-29 36788145 Cornejo-Sanchez DM 2023-02-15 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/36788145 Rare-variant association analysis reveals known and new age-related hearing loss genes. Hearing difficulty and hearing difficulty with background noise 54,853 European ancestry cases, 141,007 European ancestry controls NA Affymetrix [51873976] (imputed) 0 hearing loss http://www.ebi.ac.uk/efo/EFO_0004238 GCST90245780 Genome-wide genotyping array 2023-11-02 35027648 Dareng EO 2022-01-14 Eur J Hum Genet www.ncbi.nlm.nih.gov/pubmed/35027648 Polygenic risk modeling for prediction of epithelial ovarian cancer risk. Non-mucinous epithelial ovarian cancer 23,564 European ancestry female cases, 40,138 European ancestry female controls NA Illumina [10163797] (imputed) 0 ovarian carcinoma http://www.ebi.ac.uk/efo/EFO_0001075 GCST90016665 Genome-wide genotyping array, Targeted genotyping array [Oncoarray, ICOGS] 2023-09-21 37164147 Li C 2023-05-09 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/37164147 Exploratory factor analysis of shared and specific genetic associations in depression and anxiety. GAD-7 factor nervousness 502,656 British ancestry individuals NA NR [NR] (imputed) 2 nervousness, generalized anxiety disorder http://purl.obolibrary.org/obo/NCIT_C74532, http://www.ebi.ac.uk/efo/EFO_1001892 GCST90292532 Genome-wide genotyping array 2023-09-21 37164147 Li C 2023-05-09 Prog Neuropsychopharmacol Biol Psychiatry www.ncbi.nlm.nih.gov/pubmed/37164147 Exploratory factor analysis of shared and specific genetic associations in depression and anxiety. GAD-7 and PHQ-9 factor nervousness 502,656 British ancestry individuals NA NR [NR] (imputed) 2 nervousness, unipolar depression, generalized anxiety disorder http://purl.obolibrary.org/obo/NCIT_C74532, http://www.ebi.ac.uk/efo/EFO_0003761, http://www.ebi.ac.uk/efo/EFO_1001892 GCST90292533 Genome-wide genotyping array 2023-09-26 37543033 Ojavee SE 2023-08-01 Am J Hum Genet www.ncbi.nlm.nih.gov/pubmed/37543033 Genetic insights into the age-specific biological mechanisms governing human ovarian aging. Age at natural menopause 173,424 European ancestry women 70,082 European ancestry women NR [8747951] (imputed) 0 age at menopause http://www.ebi.ac.uk/efo/EFO_0004704 GCST90292553 Genome-wide genotyping array 2020-11-30 32916098 Verweij N 2020-09-02 Cell Syst www.ncbi.nlm.nih.gov/pubmed/32916098 The Genetic Makeup of the Electrocardiogram. Electrocardiogram morphology (amplitude at temporal datapoints) 63,706 European and unknown ancestry individuals NA Affymetrix [10000000] (imputed) 5501 electrocardiography http://www.ebi.ac.uk/efo/EFO_0004327 GCST010796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-specific 3',5'-cyclic phosphodiesterase 4C level in Chronic kidney disease with hypertension and no diabetes (20221_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-specific 3',5'-cyclic phosphodiesterase 4C in blood serum http://purl.obolibrary.org/obo/OBA_2042821 GCST90235381 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal transducer and activator of transcription 5A level in Chronic kidney disease with hypertension and no diabetes (20225_119) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of signal transducer and activator of transcription 5a in blood serum http://purl.obolibrary.org/obo/OBA_2040390 GCST90235382 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TM2 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (20229_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of TM2 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043866 GCST90235383 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uridine phosphorylase 2 level in Chronic kidney disease with hypertension and no diabetes (20231_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uridine phosphorylase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044043 GCST90235384 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptosomal-associated protein 23 level in Chronic kidney disease with hypertension and no diabetes (20241_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptosomal-associated protein 23 in blood serum http://purl.obolibrary.org/obo/OBA_2043563 GCST90235385 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Profilin-1 level in Chronic kidney disease with hypertension and no diabetes (20243_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of profilin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042855 GCST90235386 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoic acid receptor RXR-alpha level in Chronic kidney disease with hypertension and no diabetes (20245_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinoic acid receptor RXR-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043359 GCST90235387 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydropyrimidinase-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (20247_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydropyrimidinase-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041359 GCST90235388 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acylphosphatase-1 level in Chronic kidney disease with hypertension and no diabetes (20370_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of acylphosphatase-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040493 GCST90235389 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucose-induced degradation protein 8 homolog level in Chronic kidney disease with hypertension and no diabetes (20373_141) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glucose-induced degradation protein 8 homolog in blood serum http://purl.obolibrary.org/obo/OBA_2044475 GCST90235390 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative deoxyribonuclease TATDN1 level in Chronic kidney disease with hypertension and no diabetes (20376_64) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of deoxyribonuclease TATDN1 in blood serum http://purl.obolibrary.org/obo/OBA_2044640 GCST90235391 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine zipper transcription factor-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (20378_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine zipper transcription factor-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042255 GCST90235392 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small vasohibin-binding protein level in Chronic kidney disease with hypertension and no diabetes (20379_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small vasohibin-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2044656 GCST90235393 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein LSM12 homolog level in Chronic kidney disease with hypertension and no diabetes (20380_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein LSM12 in blood serum http://purl.obolibrary.org/obo/OBA_2042241 GCST90235394 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PIH1 domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (20381_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PIH1 domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044646 GCST90235395 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Motile sperm domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (20382_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of motile sperm domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044778 GCST90235396 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable RNA-binding protein 18 level in Chronic kidney disease with hypertension and no diabetes (20383_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of probable RNA-binding protein 18 in blood serum http://purl.obolibrary.org/obo/OBA_2044681 GCST90235397 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ceramide-1-phosphate transfer protein level in Chronic kidney disease with hypertension and no diabetes (20385_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ceramide-1-phosphate transfer protein in blood serum http://purl.obolibrary.org/obo/OBA_2044303 GCST90235398 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil-helix-coiled-coil-helix domain-containing protein 7 level in Chronic kidney disease with hypertension and no diabetes (20387_277) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of coiled-coil-helix-coiled-coil-helix domain-containing protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044433 GCST90235399 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial inner membrane protease subunit 2 level in Chronic kidney disease with hypertension and no diabetes (20389_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial inner membrane protease subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042020 GCST90235400 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High mobility group nucleosome-binding domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (20390_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high mobility group nucleosome-binding domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044312 GCST90235401 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma level in Chronic kidney disease with hypertension and no diabetes (20393_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma in blood serum http://purl.obolibrary.org/obo/OBA_2042823 GCST90235402 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COMM domain-containing protein 6 level in Chronic kidney disease with hypertension and no diabetes (20396_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of COMM domain-containing protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041091 GCST90235403 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxidoreductase-like domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (20399_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxidoreductase-like domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044407 GCST90235404 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BUD31 homolog level in Chronic kidney disease with hypertension and no diabetes (20401_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BUD31 in blood serum http://purl.obolibrary.org/obo/OBA_2040840 GCST90235405 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trafficking protein particle complex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (20402_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trafficking protein particle complex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044405 GCST90235406 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import receptor subunit TOM20 homolog level in Chronic kidney disease with hypertension and no diabetes (20408_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import receptor subunit TOM20 in blood serum http://purl.obolibrary.org/obo/OBA_2043901 GCST90235407 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 33 level in Chronic kidney disease with hypertension and no diabetes (20411_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tetratricopeptide repeat protein 33 in blood serum http://purl.obolibrary.org/obo/OBA_2044376 GCST90235408 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium and integrin-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (20423_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium and integrin-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041029 GCST90235409 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hematopoietically-expressed homeobox protein HHEX level in Chronic kidney disease with hypertension and no diabetes (20425_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hematopoietically-expressed homeobox protein HHEX in blood serum http://purl.obolibrary.org/obo/OBA_2041871 GCST90235410 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM84A level in Chronic kidney disease with hypertension and no diabetes (20426_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein LRATD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044619 GCST90235411 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mediator of RNA polymerase II transcription subunit 20 level in Chronic kidney disease with hypertension and no diabetes (20427_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of mediator of RNA polymerase II transcription subunit 20 in blood serum http://purl.obolibrary.org/obo/OBA_2042327 GCST90235412 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoethanolamine/phosphocholine phosphatase level in Chronic kidney disease with hypertension and no diabetes (20428_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoethanolamine/phosphocholine phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2042877 GCST90235413 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type natriuretic peptide level in Chronic kidney disease with hypertension and no diabetes (20430_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type natriuretic peptide in blood serum http://purl.obolibrary.org/obo/OBA_2042619 GCST90235414 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyroglutamyl-peptidase 1 level in Chronic kidney disease with hypertension and no diabetes (20432_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyroglutamyl-peptidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042867 GCST90235415 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (20433_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042421 GCST90235416 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Purkinje cell protein 4-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (20434_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Purkinje cell protein 4-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042804 GCST90235417 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin polyglutamylase complex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (20436_93) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin polyglutamylase complex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044655 GCST90235418 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Axonemal dynein light intermediate polypeptide 1 level in Chronic kidney disease with hypertension and no diabetes (20437_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of axonemal dynein light intermediate polypeptide 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041332 GCST90235419 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proline synthase co-transcribed bacterial homolog protein level in Chronic kidney disease with hypertension and no diabetes (20439_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyridoxal phosphate homeostasis protein PLPBP in blood serum http://purl.obolibrary.org/obo/OBA_2043037 GCST90235420 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 32 level in Chronic kidney disease with hypertension and no diabetes (20440_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tetratricopeptide repeat protein 32 in blood serum http://purl.obolibrary.org/obo/OBA_2044683 GCST90235421 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerases I, II, and III subunit RPABC1 level in Chronic kidney disease with hypertension and no diabetes (20441_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerases I, II, and III subunit RPABC1 in blood serum http://purl.obolibrary.org/obo/OBA_2042968 GCST90235422 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcipressin-3 level in Chronic kidney disease with hypertension and no diabetes (20442_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of calcipressin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043218 GCST90235423 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CST complex subunit TEN1 level in Chronic kidney disease with hypertension and no diabetes (20443_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CST complex subunit TEN1 in blood serum http://purl.obolibrary.org/obo/OBA_2044760 GCST90235424 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EH domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (25232_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EH domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041434 GCST90236869 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mannose-6-phosphate isomerase level in Chronic kidney disease with hypertension and no diabetes (25233_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mannose-6-phosphate isomerase in blood serum http://purl.obolibrary.org/obo/OBA_2042405 GCST90236870 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diphthine methyltransferase level in Chronic kidney disease with hypertension and no diabetes (25235_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diphthine methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044717 GCST90236871 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methyltransferase-like 26 level in Chronic kidney disease with hypertension and no diabetes (25236_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methyltransferase-like 26 in blood serum http://purl.obolibrary.org/obo/OBA_2044861 GCST90236872 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 5 level in Chronic kidney disease with hypertension and no diabetes (2523_31) 466 African American individuals NA Illumina [14870897] (imputed) 2 C-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008053 GCST90236873 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-lysine N-methyltransferase EEF2KMT level in Chronic kidney disease with hypertension and no diabetes (25240_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-lysine N-methyltransferase EEF2KMT in blood serum http://purl.obolibrary.org/obo/OBA_2044503 GCST90236874 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G antigen 2 level in Chronic kidney disease with hypertension and no diabetes (25413_80) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of G antigen 2B/2C in blood serum http://purl.obolibrary.org/obo/OBA_2041653 GCST90236925 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Late cornified envelope protein 3B level in Chronic kidney disease with hypertension and no diabetes (25414_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of late cornified envelope protein 3B in blood serum http://purl.obolibrary.org/obo/OBA_2042170 GCST90236926 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Periaxin level in Chronic kidney disease with hypertension and no diabetes (25416_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of periaxin in blood serum http://purl.obolibrary.org/obo/OBA_2043050 GCST90236927 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm protein associated with the nucleus on the X chromosome N4 level in Chronic kidney disease with hypertension and no diabetes (25419_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm protein associated with the nucleus on the X chromosome N4 in blood serum http://purl.obolibrary.org/obo/OBA_2043616 GCST90236928 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease P protein subunit p40 level in Chronic kidney disease with hypertension and no diabetes (25422_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonuclease P protein subunit p40 in blood serum http://purl.obolibrary.org/obo/OBA_2043328 GCST90236929 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-12 level in Chronic kidney disease with hypertension and no diabetes (25424_234) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-12 in blood serum http://purl.obolibrary.org/obo/OBA_2043750 GCST90236930 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon-related developmental regulator 1 level in Chronic kidney disease with hypertension and no diabetes (25428_103) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon-related developmental regulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041986 GCST90236931 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative methyltransferase NSUN6 level in Chronic kidney disease with hypertension and no diabetes (25433_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA (cytosine(72)-C(5))-methyltransferase NSUN6 in blood serum http://purl.obolibrary.org/obo/OBA_2044337 GCST90236932 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat and MYND domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (25437_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat and MYND domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044550 GCST90236933 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5'-nucleotidase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (25438_288) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5'-nucleotidase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044735 GCST90236934 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Type I inositol 1,4,5-trisphosphate 5-phosphatase level in Chronic kidney disease with hypertension and no diabetes (25444_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol polyphosphate-5-phosphatase A in blood serum http://purl.obolibrary.org/obo/OBA_2042031 GCST90236935 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein DDI1 homolog 2 level in Chronic kidney disease with hypertension and no diabetes (25446_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein DDI1 homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041253 GCST90236936 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional coactivator YAP1 level in Chronic kidney disease with hypertension and no diabetes (25451_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional coactivator YAP1 in blood serum http://purl.obolibrary.org/obo/OBA_2044157 GCST90236937 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myb/SANT-like DNA-binding domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (25452_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Myb/SANT-like DNA-binding domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044596 GCST90236938 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ropporin-1B level in Chronic kidney disease with hypertension and no diabetes (25453_57) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ropporin-1B in blood serum http://purl.obolibrary.org/obo/OBA_2043308 GCST90236939 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. O-acetyl-ADP-ribose deacetylase MACROD2 level in Chronic kidney disease with hypertension and no diabetes (25459_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ADP-ribose glycohydrolase MACROD2 in blood serum http://purl.obolibrary.org/obo/OBA_2044611 GCST90236940 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 5 level in Chronic kidney disease with hypertension and no diabetes (25460_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon regulatory factor 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040377 GCST90236941 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-arrestin level in Chronic kidney disease with hypertension and no diabetes (25461_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of S-arrestin in blood serum http://purl.obolibrary.org/obo/OBA_2043374 GCST90236942 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-dependent protein kinase type II-beta regulatory subunit level in Chronic kidney disease with hypertension and no diabetes (25463_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-dependent protein kinase type II-beta regulatory subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043029 GCST90236943 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome P450 2C19 level in Chronic kidney disease with hypertension and no diabetes (25464_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome P450 2C19 in blood serum http://purl.obolibrary.org/obo/OBA_2041215 GCST90236944 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Muscular LMNA-interacting protein level in Chronic kidney disease with hypertension and no diabetes (25465_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of muscular LMNA-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2044755 GCST90236945 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kynurenine 3-monooxygenase level in Chronic kidney disease with hypertension and no diabetes (25466_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kynurenine 3-monooxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2042131 GCST90236946 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SOX-9 level in Chronic kidney disease with hypertension and no diabetes (25468_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor SOX-9 in blood serum http://purl.obolibrary.org/obo/OBA_2043604 GCST90236947 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha level in Chronic kidney disease with hypertension and no diabetes (25473_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041600 GCST90236948 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat flightless-interacting protein 2 level in Chronic kidney disease with hypertension and no diabetes (25479_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat flightless-interacting protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042237 GCST90236949 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab-like protein 6 level in Chronic kidney disease with hypertension and no diabetes (25276_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab-like protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2044659 GCST90236900 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pantothenate kinase 1 level in Chronic kidney disease with hypertension and no diabetes (25277_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pantothenate kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042755 GCST90236901 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 6 level in Chronic kidney disease with hypertension and no diabetes (25278_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040655 GCST90236902 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear valosin-containing protein-like level in Chronic kidney disease with hypertension and no diabetes (25279_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear valosin-containing protein-like in blood serum http://purl.obolibrary.org/obo/OBA_2042680 GCST90236903 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (25280_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LIM domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044326 GCST90236904 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Antizyme inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (25282_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of antizyme inhibitor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040743 GCST90236905 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catenin alpha-3 level in Chronic kidney disease with hypertension and no diabetes (25283_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of catenin alpha-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041188 GCST90236906 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like modifier-activating enzyme 6 level in Chronic kidney disease with hypertension and no diabetes (25284_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like modifier-activating enzyme 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043983 GCST90236907 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch repeat and BTB domain-containing protein 11 level in Chronic kidney disease with hypertension and no diabetes (25285_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch repeat and BTB domain-containing protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2044743 GCST90236908 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab GTPase-activating protein 1-like level in Chronic kidney disease with hypertension and no diabetes (25286_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab GTPase-activating protein 1-like in blood serum http://purl.obolibrary.org/obo/OBA_2043175 GCST90236909 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4 gamma 1 level in Chronic kidney disease with hypertension and no diabetes (25287_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 4 gamma 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041456 GCST90236910 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dimethylaniline monooxygenase [N-oxide-forming] 3 level in Chronic kidney disease with hypertension and no diabetes (25288_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of flavin-containing monooxygenase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041596 GCST90236911 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family M member 2 level in Chronic kidney disease with hypertension and no diabetes (25291_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family M member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044599 GCST90236912 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxylesterase 3 level in Chronic kidney disease with hypertension and no diabetes (25292_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxylesterase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044536 GCST90236913 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxylesterase 3 level in Chronic kidney disease with hypertension and no diabetes (25292_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of carboxylesterase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044536 GCST90236914 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiomotin level in Chronic kidney disease with hypertension and no diabetes (25296_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of angiomotin in blood serum http://purl.obolibrary.org/obo/OBA_2040581 GCST90236915 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 and PX domain-containing protein 2B level in Chronic kidney disease with hypertension and no diabetes (25297_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of SH3 and PX domain-containing protein 2B in blood serum http://purl.obolibrary.org/obo/OBA_2043496 GCST90236916 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysine-specific demethylase 4C level in Chronic kidney disease with hypertension and no diabetes (25298_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysine-specific demethylase 4C in blood serum http://purl.obolibrary.org/obo/OBA_2042071 GCST90236917 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor coactivator 7 level in Chronic kidney disease with hypertension and no diabetes (25299_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor coactivator 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042531 GCST90236918 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mucosa-associated lymphoid tissue lymphoma translocation protein 1 level in Chronic kidney disease with hypertension and no diabetes (25300_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mucosa-associated lymphoid tissue lymphoma translocation protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042274 GCST90236919 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity tyrosine-phosphorylation-regulated kinase 1A level in Chronic kidney disease with hypertension and no diabetes (25301_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity tyrosine-phosphorylation-regulated kinase 1A in blood serum http://purl.obolibrary.org/obo/OBA_2041397 GCST90236920 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DAXX level in Chronic kidney disease with hypertension and no diabetes (25306_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of death domain-associated protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041233 GCST90236921 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WD repeat-containing protein 18 level in Chronic kidney disease with hypertension and no diabetes (25307_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of WD repeat-containing protein 18 in blood serum http://purl.obolibrary.org/obo/OBA_2044380 GCST90236922 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain kinase 1 level in Chronic kidney disease with hypertension and no diabetes (25308_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of LIM domain kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042203 GCST90236923 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 140 level in Chronic kidney disease with hypertension and no diabetes (25409_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 140 in blood serum http://purl.obolibrary.org/obo/OBA_2044569 GCST90236924 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urea transporter 1 level in Chronic kidney disease with hypertension and no diabetes (13430_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of urea transporter 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043524 GCST90233869 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane protein FAM159A level in Chronic kidney disease with hypertension and no diabetes (13431_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein shisa-like-2A in blood serum http://purl.obolibrary.org/obo/OBA_2044793 GCST90233870 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protrudin level in Chronic kidney disease with hypertension and no diabetes (13432_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233871 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-parvin level in Chronic kidney disease with hypertension and no diabetes (13434_172) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-parvin in blood serum http://purl.obolibrary.org/obo/OBA_2042765 GCST90233872 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-20 receptor subunit beta level in Chronic kidney disease with hypertension and no diabetes (13435_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-20 receptor subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2042012 GCST90233873 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myc-associated zinc finger protein level in Chronic kidney disease with hypertension and no diabetes (13436_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Myc-associated zinc finger protein in blood serum http://purl.obolibrary.org/obo/OBA_2042308 GCST90233874 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chordin level in Chronic kidney disease with hypertension and no diabetes (13438_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chordin in blood serum http://purl.obolibrary.org/obo/OBA_2040184 GCST90233875 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IQ domain-containing protein F3 level in Chronic kidney disease with hypertension and no diabetes (13439_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of IQ domain-containing protein F3 in blood serum http://purl.obolibrary.org/obo/OBA_2044779 GCST90233876 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dixin level in Chronic kidney disease with hypertension and no diabetes (13441_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dixin in blood serum http://purl.obolibrary.org/obo/OBA_2041305 GCST90233877 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Shadow of prion protein level in Chronic kidney disease with hypertension and no diabetes (13447_42) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of shadow of prion protein in blood serum http://purl.obolibrary.org/obo/OBA_2043645 GCST90233878 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Splicing factor 3B subunit 4 level in Chronic kidney disease with hypertension and no diabetes (13449_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of splicing factor 3B subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043474 GCST90233879 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 8 level in Chronic kidney disease with hypertension and no diabetes (13450_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044068 GCST90233880 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibronectin type III domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (13451_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibronectin type III domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044462 GCST90233881 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small integral membrane protein 13 level in Chronic kidney disease with hypertension and no diabetes (13452_113) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small integral membrane protein 13 in blood serum http://purl.obolibrary.org/obo/OBA_2044822 GCST90233882 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L33, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (13453_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L33, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042429 GCST90233883 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ETS-related transcription factor Elf-5 level in Chronic kidney disease with hypertension and no diabetes (13457_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ETS-related transcription factor Elf-5 in blood serum http://purl.obolibrary.org/obo/OBA_2041465 GCST90233884 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Torsin-4A level in Chronic kidney disease with hypertension and no diabetes (13459_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of torsin-4A in blood serum http://purl.obolibrary.org/obo/OBA_2044757 GCST90233885 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chondroadherin level in Chronic kidney disease with hypertension and no diabetes (13460_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chondroadherin in blood serum http://purl.obolibrary.org/obo/OBA_2041000 GCST90233886 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxidasin homolog level in Chronic kidney disease with hypertension and no diabetes (13463_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxidasin in blood serum http://purl.obolibrary.org/obo/OBA_2043120 GCST90233887 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nutritionally-regulated adipose and cardiac enriched protein homolog level in Chronic kidney disease with hypertension and no diabetes (13464_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nutritionally-regulated adipose and cardiac enriched protein homolog in blood serum http://purl.obolibrary.org/obo/OBA_2044845 GCST90233888 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcipressin-1 level in Chronic kidney disease with hypertension and no diabetes (13465_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcipressin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043216 GCST90233889 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Parathyroid hormone/parathyroid hormone-related peptide receptor level in Chronic kidney disease with hypertension and no diabetes (13470_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of parathyroid hormone/parathyroid hormone-related peptide receptor in blood serum http://purl.obolibrary.org/obo/OBA_2043095 GCST90233890 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Haloacid dehalogenase-like hydrolase domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (13472_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of haloacid dehalogenase-like hydrolase domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044675 GCST90233891 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Laminin subunit alpha-3 level in Chronic kidney disease with hypertension and no diabetes (20074_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of laminin subunit alpha-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042157 GCST90235329 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 4 level in Chronic kidney disease with hypertension and no diabetes (20075_130) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042266 GCST90235330 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin light chain 6B level in Chronic kidney disease with hypertension and no diabetes (20078_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin light chain 6B in blood serum http://purl.obolibrary.org/obo/OBA_2042482 GCST90235331 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoenolpyruvate carboxykinase [GTP], mitochondrial level in Chronic kidney disease with hypertension and no diabetes (20079_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of phosphoenolpyruvate carboxykinase [GTP], mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042800 GCST90235332 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase Pim-2 level in Chronic kidney disease with hypertension and no diabetes (20081_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase Pim-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042893 GCST90235333 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-6A level in Chronic kidney disease with hypertension and no diabetes (20083_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-6A in blood serum http://purl.obolibrary.org/obo/OBA_2043169 GCST90235334 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-11B level in Chronic kidney disease with hypertension and no diabetes (20086_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-11B in blood serum http://purl.obolibrary.org/obo/OBA_2043138 GCST90235335 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 15 kDa selenoprotein level in Chronic kidney disease with hypertension and no diabetes (20087_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of selenoprotein F in blood serum http://purl.obolibrary.org/obo/OBA_2043443 GCST90235336 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfotransferase 1C4 level in Chronic kidney disease with hypertension and no diabetes (20089_172) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 1C4 in blood serum http://purl.obolibrary.org/obo/OBA_2043728 GCST90235337 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 E3 level in Chronic kidney disease with hypertension and no diabetes (20090_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 E3 in blood serum http://purl.obolibrary.org/obo/OBA_2043994 GCST90235338 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A1 level in Chronic kidney disease with hypertension and no diabetes (20091_138) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ephrin-A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041422 GCST90235339 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular cell adhesion protein 1 level in Chronic kidney disease with hypertension and no diabetes (20093_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 vascular cell adhesion protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020846 GCST90235340 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin light polypeptide 6 level in Chronic kidney disease with hypertension and no diabetes (20105_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin light polypeptide 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042481 GCST90235341 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger mRNA-decapping enzyme DcpS level in Chronic kidney disease with hypertension and no diabetes (20106_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of scavenger mRNA-decapping enzyme DcpS in blood serum http://purl.obolibrary.org/obo/OBA_2041243 GCST90235342 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin light polypeptide 4 level in Chronic kidney disease with hypertension and no diabetes (20107_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin light chain 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042479 GCST90235343 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hematological and neurological expressed 1-like protein level in Chronic kidney disease with hypertension and no diabetes (20110_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of jupiter microtubule associated homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041899 GCST90235344 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brain acid soluble protein 1 level in Chronic kidney disease with hypertension and no diabetes (20111_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of brain acid soluble protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040778 GCST90235345 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase OSR1 level in Chronic kidney disease with hypertension and no diabetes (20116_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase OSR1 in blood serum http://purl.obolibrary.org/obo/OBA_2042728 GCST90235346 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4E-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (20117_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 eukaryotic translation initiation factor 4E-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020368 GCST90235347 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amphoterin-induced protein 1 level in Chronic kidney disease with hypertension and no diabetes (20120_101) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235348 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glial fibrillary acidic protein level in Chronic kidney disease with hypertension and no diabetes (20126_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90235349 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hephaestin level in Chronic kidney disease with hypertension and no diabetes (20127_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hephaestin in blood serum http://purl.obolibrary.org/obo/OBA_2041857 GCST90235350 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP response element-binding protein level in Chronic kidney disease with hypertension and no diabetes (20128_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-responsive element-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041131 GCST90235351 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase I isoform gamma-1 level in Chronic kidney disease with hypertension and no diabetes (20130_144) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of casein kinase I isoform gamma-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041171 GCST90235352 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 3 level in Chronic kidney disease with hypertension and no diabetes (20133_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042265 GCST90235353 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage receptor MARCO level in Chronic kidney disease with hypertension and no diabetes (20134_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of macrophage receptor MARCO in blood serum http://purl.obolibrary.org/obo/OBA_2040348 GCST90235354 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. mRNA-capping enzyme level in Chronic kidney disease with hypertension and no diabetes (20135_85) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of mRNA-capping enzyme in blood serum http://purl.obolibrary.org/obo/OBA_2043301 GCST90235355 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ciliogenesis-associated TTC17-interacting protein level in Chronic kidney disease with hypertension and no diabetes (25242_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ciliogenesis-associated TTC17-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2044837 GCST90236875 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable E3 ubiquitin-protein ligase HECTD3 level in Chronic kidney disease with hypertension and no diabetes (25244_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase HECTD3 in blood serum http://purl.obolibrary.org/obo/OBA_2044444 GCST90236876 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synembryn-A level in Chronic kidney disease with hypertension and no diabetes (25245_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synembryn-A in blood serum http://purl.obolibrary.org/obo/OBA_2043272 GCST90236877 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Armadillo repeat-containing protein 8 level in Chronic kidney disease with hypertension and no diabetes (25247_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of armadillo repeat-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044451 GCST90236878 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein numb homolog level in Chronic kidney disease with hypertension and no diabetes (25248_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein numb in blood serum http://purl.obolibrary.org/obo/OBA_2042675 GCST90236879 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High mobility group protein B1 level in Chronic kidney disease with hypertension and no diabetes (2524_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 high mobility group protein B1 measurement http://www.ebi.ac.uk/efo/EFO_0020449 GCST90236880 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MTSS1-like protein level in Chronic kidney disease with hypertension and no diabetes (25252_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein MTSS 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042457 GCST90236881 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein G(s) subunit alpha isoforms level in Chronic kidney disease with hypertension and no diabetes (25253_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90236882 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane and ubiquitin-like domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (25255_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane and ubiquitin-like domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043886 GCST90236883 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elongation factor 1-alpha 1 level in Chronic kidney disease with hypertension and no diabetes (25256_153) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of elongation factor 1-alpha 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041418 GCST90236884 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elongation factor 1-alpha 1 level in Chronic kidney disease with hypertension and no diabetes (25256_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of elongation factor 1-alpha 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041418 GCST90236885 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oligodendrocyte transcription factor 1 level in Chronic kidney disease with hypertension and no diabetes (25257_162) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oligodendrocyte transcription factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042705 GCST90236886 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermatogenesis-associated protein 5 level in Chronic kidney disease with hypertension and no diabetes (25258_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosome biogenesis protein SPATA5 in blood serum http://purl.obolibrary.org/obo/OBA_2043619 GCST90236887 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C17orf62 level in Chronic kidney disease with hypertension and no diabetes (25259_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome b-245 chaperone 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044863 GCST90236888 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C15orf17 level in Chronic kidney disease with hypertension and no diabetes (25260_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM219B in blood serum http://purl.obolibrary.org/obo/OBA_2044637 GCST90236889 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat and SAM domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (25261_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat and SAM domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044581 GCST90236890 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 24 level in Chronic kidney disease with hypertension and no diabetes (25263_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2040650 GCST90236891 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SHIP level in Chronic kidney disease with hypertension and no diabetes (25264_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040434 GCST90236892 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Formin-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (25265_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of formin-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041599 GCST90236893 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxysterol-binding protein-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (25266_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxysterol-binding protein-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042713 GCST90236894 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable transcription factor PML level in Chronic kidney disease with hypertension and no diabetes (25270_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor PML in blood serum http://purl.obolibrary.org/obo/OBA_2044234 GCST90236895 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-23 level in Chronic kidney disease with hypertension and no diabetes (25272_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-23 in blood serum http://purl.obolibrary.org/obo/OBA_2040961 GCST90236896 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caldesmon level in Chronic kidney disease with hypertension and no diabetes (25273_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caldesmon in blood serum http://purl.obolibrary.org/obo/OBA_2040879 GCST90236897 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (25274_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040592 GCST90236898 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone deacetylase 4 level in Chronic kidney disease with hypertension and no diabetes (25275_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone deacetylase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041847 GCST90236899 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein A1 level in Chronic kidney disease with hypertension and no diabetes (20137_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041903 GCST90235356 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endophilin-A1 level in Chronic kidney disease with hypertension and no diabetes (20139_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endophilin-A1 in blood serum http://purl.obolibrary.org/obo/OBA_2043491 GCST90235357 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein 2 level in Chronic kidney disease with hypertension and no diabetes (20141_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043802 GCST90235358 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 C level in Chronic kidney disease with hypertension and no diabetes (20142_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 C in blood serum http://purl.obolibrary.org/obo/OBA_2043991 GCST90235359 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuritin-like protein level in Chronic kidney disease with hypertension and no diabetes (20159_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuritin-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042641 GCST90235360 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neural cell adhesion molecule 1 level in Chronic kidney disease with hypertension and no diabetes (20161_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neural cell adhesion molecule 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040231 GCST90235361 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydropyrimidinase level in Chronic kidney disease with hypertension and no diabetes (20165_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydropyrimidinase in blood serum http://purl.obolibrary.org/obo/OBA_2041356 GCST90235362 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpain-9 level in Chronic kidney disease with hypertension and no diabetes (20173_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calpain-9 in blood serum http://purl.obolibrary.org/obo/OBA_2040891 GCST90235363 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-3(IX) chain level in Chronic kidney disease with hypertension and no diabetes (20175_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-3(IX) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041088 GCST90235364 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-11 level in Chronic kidney disease with hypertension and no diabetes (20181_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin alpha-11 in blood serum http://purl.obolibrary.org/obo/OBA_2042045 GCST90235365 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein MOX-1 level in Chronic kidney disease with hypertension and no diabetes (20183_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein MOX-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042337 GCST90235366 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (20185_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041307 GCST90235367 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha V beta 3 level in Chronic kidney disease with hypertension and no diabetes (20187_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802637 GCST90235368 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha V beta 6 level in Chronic kidney disease with hypertension and no diabetes (20189_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802637 GCST90235369 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha V beta 6 level in Chronic kidney disease with hypertension and no diabetes (20189_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802637 GCST90235370 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha V beta 8 level in Chronic kidney disease with hypertension and no diabetes (20191_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-5 measurement http://www.ebi.ac.uk/efo/EFO_0802637 GCST90235371 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon-induced helicase C domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (20195_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon-induced helicase C domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041975 GCST90235372 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Visinin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (20197_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of visinin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044116 GCST90235373 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1s subcomponent level in Chronic kidney disease with hypertension and no diabetes (20203_45) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement C1s subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008091 GCST90235374 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity tyrosine-phosphorylation-regulated kinase 2 level in Chronic kidney disease with hypertension and no diabetes (20205_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity tyrosine-phosphorylation-regulated kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041398 GCST90235375 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylate-binding protein 5 level in Chronic kidney disease with hypertension and no diabetes (20211_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanylate-binding protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041682 GCST90235376 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 6 level in Chronic kidney disease with hypertension and no diabetes (20213_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock 70 kDa protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041948 GCST90235377 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-V: beta-1 complex level in Chronic kidney disease with hypertension and no diabetes (20215_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-V: beta-5 complex measurement http://www.ebi.ac.uk/efo/EFO_0020480 GCST90235378 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lamin-B2 level in Chronic kidney disease with hypertension and no diabetes (20217_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lamin-B2 in blood serum http://purl.obolibrary.org/obo/OBA_2042212 GCST90235379 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neprilysin level in Chronic kidney disease with hypertension and no diabetes (20219_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neprilysin in blood serum http://purl.obolibrary.org/obo/OBA_2040351 GCST90235380 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal growth regulator 1 level in Chronic kidney disease with hypertension and no diabetes (13109_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuronal growth regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0021932 GCST90233819 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell lymphoma 6 protein level in Chronic kidney disease with hypertension and no diabetes (13111_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 B-cell lymphoma 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0021933 GCST90233820 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follistatin-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (13112_179) 466 African American individuals NA Illumina [14870897] (imputed) 0 follistatin-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021934 GCST90233821 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteopontin level in Chronic kidney disease with hypertension and no diabetes (13113_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 osteopontin measurement http://www.ebi.ac.uk/efo/EFO_0021776 GCST90233822 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lumican level in Chronic kidney disease with hypertension and no diabetes (13114_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 lumican measurement http://www.ebi.ac.uk/efo/EFO_0021889 GCST90233823 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD177 antigen level in Chronic kidney disease with hypertension and no diabetes (13116_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 cD177 antigen measurement http://www.ebi.ac.uk/efo/EFO_0021866 GCST90233824 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Choline/ethanolamine kinase level in Chronic kidney disease with hypertension and no diabetes (13117_232) 466 African American individuals NA Illumina [14870897] (imputed) 1 choline/ethanolamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0021935 GCST90233825 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPARC-related modular calcium-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (13118_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 sPARC-related modular calcium-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021868 GCST90233826 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Z-dependent protease inhibitor level in Chronic kidney disease with hypertension and no diabetes (13119_26) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90233827 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane protein FLRT2 level in Chronic kidney disease with hypertension and no diabetes (13122_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine-rich repeat transmembrane protein FLRT2 measurement http://www.ebi.ac.uk/efo/EFO_0021860 GCST90233828 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane protein FLRT3 level in Chronic kidney disease with hypertension and no diabetes (13123_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90233829 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily containing leucine-rich repeat protein 2 level in Chronic kidney disease with hypertension and no diabetes (13124_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 immunoglobulin superfamily containing leucine-rich repeat protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021879 GCST90233830 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitronectin level in Chronic kidney disease with hypertension and no diabetes (13125_45) 466 African American individuals NA Illumina [14870897] (imputed) 1 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90233831 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmocollin-2 level in Chronic kidney disease with hypertension and no diabetes (13126_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 desmocollin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021936 GCST90233832 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor level in Chronic kidney disease with hypertension and no diabetes (13129_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 low-density lipoprotein receptor measurement http://www.ebi.ac.uk/efo/EFO_0021937 GCST90233833 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hexokinase-1 level in Chronic kidney disease with hypertension and no diabetes (13131_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 hexokinase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021939 GCST90233834 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-5A level in Chronic kidney disease with hypertension and no diabetes (13132_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 semaphorin-5A measurement http://www.ebi.ac.uk/efo/EFO_0021864 GCST90233835 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Latent-transforming growth factor beta-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (13133_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 latent-transforming growth factor beta-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0021940 GCST90233836 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase Mdm2 level in Chronic kidney disease with hypertension and no diabetes (13228_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 e3 ubiquitin-protein ligase mdm2 measurement http://www.ebi.ac.uk/efo/EFO_0020340 GCST90233837 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Mdm4 level in Chronic kidney disease with hypertension and no diabetes (13229_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein Mdm4 in blood serum http://purl.obolibrary.org/obo/OBA_2042320 GCST90233838 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ig gamma-2, Kappa level in Chronic kidney disease with hypertension and no diabetes (13230_174) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin heavy constant gamma 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041994 GCST90233839 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ig gamma-4, Kappa level in Chronic kidney disease with hypertension and no diabetes (13231_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin heavy constant gamma 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041995 GCST90233840 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-3a level in Chronic kidney disease with hypertension and no diabetes (13236_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein wnt-7a measurement http://www.ebi.ac.uk/efo/EFO_0020689 GCST90233841 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 and multiple ankyrin repeat domains protein 1 level in Chronic kidney disease with hypertension and no diabetes (13240_170) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH3 and multiple ankyrin repeat domains protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043497 GCST90233842 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 and multiple ankyrin repeat domains protein 3 level in Chronic kidney disease with hypertension and no diabetes (13242_134) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH3 and multiple ankyrin repeat domains protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043498 GCST90233843 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukemia inhibitory factor receptor level in Chronic kidney disease with hypertension and no diabetes (5837_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 leukemia inhibitory factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0010788 GCST90238103 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase EHMT2 level in Chronic kidney disease with hypertension and no diabetes (5843_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone-lysine n-methyltransferase EHMT2 measurement http://www.ebi.ac.uk/efo/EFO_0020455 GCST90238104 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noggin level in Chronic kidney disease with hypertension and no diabetes (5846_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 noggin measurement http://www.ebi.ac.uk/efo/EFO_0021995 GCST90238105 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A12 level in Chronic kidney disease with hypertension and no diabetes (5852_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein S100-A12 measurement http://www.ebi.ac.uk/efo/EFO_0010925 GCST90238106 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated protein tau level in Chronic kidney disease with hypertension and no diabetes (5854_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 microtubule-associated protein tau http://www.ebi.ac.uk/efo/EFO_0005816 GCST90238107 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein zeta/delta level in Chronic kidney disease with hypertension and no diabetes (5858_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 14-3-3 protein zeta/delta measurement http://www.ebi.ac.uk/efo/EFO_0021996 GCST90238108 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-hydroxyanthranilate 3,4-dioxygenase level in Chronic kidney disease with hypertension and no diabetes (5861_78) 466 African American individuals NA Illumina [14870897] (imputed) 1 3-hydroxyanthranilate 3,4-dioxygenase measurement http://www.ebi.ac.uk/efo/EFO_0021862 GCST90238109 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arginase-1 level in Chronic kidney disease with hypertension and no diabetes (5867_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 arginase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020160 GCST90238110 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bcl2-associated agonist of cell death level in Chronic kidney disease with hypertension and no diabetes (5870_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 bcl2-associated agonist of cell death measurement http://www.ebi.ac.uk/efo/EFO_0021998 GCST90238111 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynactin subunit 2 level in Chronic kidney disease with hypertension and no diabetes (5879_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 dynactin subunit 2 measurement http://www.ebi.ac.uk/efo/EFO_0020338 GCST90238112 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elongation factor 1-beta level in Chronic kidney disease with hypertension and no diabetes (5882_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 elongation factor 1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020345 GCST90238113 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4H level in Chronic kidney disease with hypertension and no diabetes (5885_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 eukaryotic translation initiation factor 4H measurement http://www.ebi.ac.uk/efo/EFO_0021999 GCST90238114 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 5A-1 level in Chronic kidney disease with hypertension and no diabetes (5888_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 eukaryotic translation initiation factor 5A-1 measurement http://www.ebi.ac.uk/efo/EFO_0020370 GCST90238115 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastrin-releasing peptide level in Chronic kidney disease with hypertension and no diabetes (5897_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 gastrin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0022000 GCST90238116 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histidine triad nucleotide-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (5900_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 histidine triad nucleotide-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020450 GCST90238117 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock cognate 71 kDa protein level in Chronic kidney disease with hypertension and no diabetes (5903_91) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock cognate 71 kda protein measurement http://www.ebi.ac.uk/efo/EFO_0020434 GCST90238118 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleoside diphosphate kinase A level in Chronic kidney disease with hypertension and no diabetes (5909_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 nucleoside diphosphate kinase A measurement http://www.ebi.ac.uk/efo/EFO_0009947 GCST90238119 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal targeting signal 1 receptor level in Chronic kidney disease with hypertension and no diabetes (5915_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 peroxisomal targeting signal 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0022001 GCST90238120 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome activator complex subunit 1 level in Chronic kidney disease with hypertension and no diabetes (5918_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 proteasome activator complex subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0020661 GCST90238121 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WNT1-inducible-signaling pathway protein 3 level in Chronic kidney disease with hypertension and no diabetes (5927_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 WNT1-inducible-signaling pathway protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0022003 GCST90238122 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Troponin I, cardiac muscle level in Chronic kidney disease with hypertension and no diabetes (5930_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 troponin i, cardiac muscle measurement http://www.ebi.ac.uk/efo/EFO_0020788 GCST90238123 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ferritin level in Chronic kidney disease with hypertension and no diabetes (5934_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 ferritin measurement http://www.ebi.ac.uk/efo/EFO_0004459 GCST90238124 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor level in Chronic kidney disease with hypertension and no diabetes (5936_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90238125 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 12 level in Chronic kidney disease with hypertension and no diabetes (5939_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 12 measurement http://www.ebi.ac.uk/efo/EFO_0010801 GCST90238126 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombopoietin level in Chronic kidney disease with hypertension and no diabetes (5947_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 thrombopoietin measurement http://www.ebi.ac.uk/efo/EFO_0022004 GCST90238127 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U8 snoRNA-decapping enzyme level in Chronic kidney disease with hypertension and no diabetes (20948_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U8 snoRNA-decapping enzyme in blood serum http://purl.obolibrary.org/obo/OBA_2042667 GCST90235517 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoribosyltransferase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (20950_159) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoribosyltransferase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044762 GCST90235518 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methylmalonic aciduria and homocystinuria type C protein level in Chronic kidney disease with hypertension and no diabetes (20953_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyanocobalamin reductase / alkylcobalamin dealkylase in blood serum http://purl.obolibrary.org/obo/OBA_2042384 GCST90235519 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein LDOC1L level in Chronic kidney disease with hypertension and no diabetes (20954_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retrotransposon Gag-like protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042185 GCST90235520 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA-specific adenosine deaminase 2 level in Chronic kidney disease with hypertension and no diabetes (20955_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA-specific adenosine deaminase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040509 GCST90235521 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (2570_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90236965 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (2571_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-like growth factor-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041990 GCST90236966 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-6 level in Chronic kidney disease with hypertension and no diabetes (2573_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90236967 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leptin level in Chronic kidney disease with hypertension and no diabetes (2575_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90236968 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-9 level in Chronic kidney disease with hypertension and no diabetes (2579_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrix metalloproteinase-9 measurement http://www.ebi.ac.uk/efo/EFO_0020561 GCST90236969 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myeloperoxidase level in Chronic kidney disease with hypertension and no diabetes (2580_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 myeloperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0005243 GCST90236970 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolactin level in Chronic kidney disease with hypertension and no diabetes (2585_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 prolactin measurement http://www.ebi.ac.uk/efo/EFO_0007003 GCST90236971 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone acetyltransferase KAT5 level in Chronic kidney disease with hypertension and no diabetes (25879_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone acetyltransferase KAT5 in blood serum http://purl.obolibrary.org/obo/OBA_2041955 GCST90236972 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5-Lipoxygenase level in Chronic kidney disease with hypertension and no diabetes (25880_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyunsaturated fatty acid 5-lipoxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2040573 GCST90236973 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-binding cassette sub-family D member 4 level in Chronic kidney disease with hypertension and no diabetes (25886_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysosomal cobalamin transporter ABCD4 in blood serum http://purl.obolibrary.org/obo/OBA_2044544 GCST90236974 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Absent in melanoma 2 level in Chronic kidney disease with hypertension and no diabetes (25889_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon-inducible protein AIM2 in blood serum http://purl.obolibrary.org/obo/OBA_2040543 GCST90236975 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-5 level in Chronic kidney disease with hypertension and no diabetes (25895_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of caspase-5 in blood serum http://purl.obolibrary.org/obo/OBA_2040408 GCST90236976 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chitinase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (25898_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chitinase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044522 GCST90236977 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CREB-regulated transcription coactivator 3 level in Chronic kidney disease with hypertension and no diabetes (25901_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CREB-regulated transcription coactivator 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041153 GCST90236978 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate dehydrogenase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (25902_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamate dehydrogenase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041738 GCST90236979 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dedicator of cytokinesis protein 2 level in Chronic kidney disease with hypertension and no diabetes (25904_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dedicator of cytokinesis protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041340 GCST90236980 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elongation factor 1-alpha 1 level in Chronic kidney disease with hypertension and no diabetes (25906_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of elongation factor 1-alpha 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041418 GCST90236981 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Echinoderm microtubule-associated protein-like 2 level in Chronic kidney disease with hypertension and no diabetes (25907_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of echinoderm microtubule-associated protein-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041474 GCST90236982 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive tyrosine-protein kinase transmembrane receptor ROR1 level in Chronic kidney disease with hypertension and no diabetes (2590_69) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tyrosine-protein kinase transmembrane receptor ROR1 in blood serum http://purl.obolibrary.org/obo/OBA_2043309 GCST90236983 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FK506 binding protein 1A level in Chronic kidney disease with hypertension and no diabetes (25912_131) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase FKBP1A in blood serum http://purl.obolibrary.org/obo/OBA_2041587 GCST90236984 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Latexin level in Chronic kidney disease with hypertension and no diabetes (20592_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of latexin in blood serum http://purl.obolibrary.org/obo/OBA_2042247 GCST90235492 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-galactosyltransferase 5 level in Chronic kidney disease with hypertension and no diabetes (20593_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-galactosyltransferase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040747 GCST90235493 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pseudouridine-5'-phosphatase level in Chronic kidney disease with hypertension and no diabetes (20912_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pseudouridine-5'-phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2044310 GCST90235494 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 1 level in Chronic kidney disease with hypertension and no diabetes (20913_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041438 GCST90235495 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adaptin ear-binding coat-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (20915_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adaptin ear-binding coat-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042550 GCST90235496 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U1 small nuclear ribonucleoprotein C level in Chronic kidney disease with hypertension and no diabetes (20918_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U1 small nuclear ribonucleoprotein C in blood serum http://purl.obolibrary.org/obo/OBA_2043574 GCST90235497 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ domain-containing protein GIPC2 level in Chronic kidney disease with hypertension and no diabetes (20921_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of PDZ domain-containing protein GIPC2 in blood serum http://purl.obolibrary.org/obo/OBA_2044608 GCST90235498 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Profilin-4 level in Chronic kidney disease with hypertension and no diabetes (20922_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of profilin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042857 GCST90235499 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Magnesium-dependent phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (20923_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of magnesium-dependent phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042321 GCST90235500 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein-like 1 level in Chronic kidney disease with hypertension and no diabetes (20924_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043804 GCST90235501 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-dependent transcription factor ATF-1 level in Chronic kidney disease with hypertension and no diabetes (20926_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-dependent transcription factor ATF-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040712 GCST90235502 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. General transcription factor IIF subunit 2 level in Chronic kidney disease with hypertension and no diabetes (20927_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of general transcription factor IIF subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041815 GCST90235503 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein-like 7 level in Chronic kidney disease with hypertension and no diabetes (20928_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein-like 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043809 GCST90235504 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CTD small phosphatase-like protein level in Chronic kidney disease with hypertension and no diabetes (20929_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CTD small phosphatase-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2041183 GCST90235505 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methylglutaconyl-CoA hydratase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (20931_156) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methylglutaconyl-CoA hydratase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040739 GCST90235506 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 69 level in Chronic kidney disease with hypertension and no diabetes (20932_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 69 in blood serum http://purl.obolibrary.org/obo/OBA_2044411 GCST90235507 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-24 level in Chronic kidney disease with hypertension and no diabetes (20934_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-24 in blood serum http://purl.obolibrary.org/obo/OBA_2043147 GCST90235508 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosducin-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (20935_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosducin-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042818 GCST90235509 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative deoxyribonuclease TATDN3 level in Chronic kidney disease with hypertension and no diabetes (20936_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative deoxyribonuclease TATDN3 in blood serum http://purl.obolibrary.org/obo/OBA_2044587 GCST90235510 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. H/ACA ribonucleoprotein complex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (20939_113) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of H/ACA ribonucleoprotein complex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042579 GCST90235511 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (20941_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044008 GCST90235512 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 8 level in Chronic kidney disease with hypertension and no diabetes (20942_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044483 GCST90235513 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-alpha-acetyltransferase 50 level in Chronic kidney disease with hypertension and no diabetes (20943_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-alpha-acetyltransferase 50 in blood serum http://purl.obolibrary.org/obo/OBA_2042515 GCST90235514 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gametocyte-specific factor 1 level in Chronic kidney disease with hypertension and no diabetes (20946_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gametocyte-specific factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041819 GCST90235515 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Dr1 level in Chronic kidney disease with hypertension and no diabetes (20947_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Dr1 in blood serum http://purl.obolibrary.org/obo/OBA_2041361 GCST90235516 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A disintegrin and metalloproteinase with thrombospondin motifs 6 level in Chronic kidney disease with hypertension and no diabetes (6441_62) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of a disintegrin and metalloproteinase with thrombospondin motifs 6 in blood serum http://purl.obolibrary.org/obo/OBA_2044706 GCST90238275 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B melanoma antigen 3 level in Chronic kidney disease with hypertension and no diabetes (6442_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B melanoma antigen 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040771 GCST90238276 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 3 level in Chronic kidney disease with hypertension and no diabetes (6444_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pregnancy-specific beta-1-glycoprotein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043058 GCST90238277 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pentraxin-related protein PTX3 level in Chronic kidney disease with hypertension and no diabetes (6447_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 pentraxin-related protein PTX3 measurement http://www.ebi.ac.uk/efo/EFO_0010923 GCST90238278 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-3C level in Chronic kidney disease with hypertension and no diabetes (6448_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-3C in blood serum http://purl.obolibrary.org/obo/OBA_2043428 GCST90238279 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastrotropin level in Chronic kidney disease with hypertension and no diabetes (6450_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gastrotropin in blood serum http://purl.obolibrary.org/obo/OBA_2041539 GCST90238280 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Asporin level in Chronic kidney disease with hypertension and no diabetes (6451_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of asporin in blood serum http://purl.obolibrary.org/obo/OBA_2040706 GCST90238281 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily B member 4 level in Chronic kidney disease with hypertension and no diabetes (6453_70) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily B member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042200 GCST90238282 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GDP-dissociation inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (6454_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 rab gdp dissociation inhibitor beta measurement http://www.ebi.ac.uk/efo/EFO_0020697 GCST90238283 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hyaluronan and proteoglycan link protein 4 level in Chronic kidney disease with hypertension and no diabetes (6455_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hyaluronan and proteoglycan link protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041837 GCST90238284 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 6 level in Chronic kidney disease with hypertension and no diabetes (6456_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pregnancy-specific beta-1-glycoprotein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043061 GCST90238285 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin gamma-A1 level in Chronic kidney disease with hypertension and no diabetes (6457_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protocadherin gamma-A1 in blood serum http://purl.obolibrary.org/obo/OBA_2042792 GCST90238286 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein C-III level in Chronic kidney disease with hypertension and no diabetes (6461_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apolipoprotein C-III in blood serum http://purl.obolibrary.org/obo/OBA_2040626 GCST90238287 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metalloproteinase inhibitor 4 level in Chronic kidney disease with hypertension and no diabetes (6462_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of metalloproteinase inhibitor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043856 GCST90238288 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Orexigenic neuropeptide QRFP level in Chronic kidney disease with hypertension and no diabetes (6463_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of orexigenic neuropeptide QRFP in blood serum http://purl.obolibrary.org/obo/OBA_2043134 GCST90238289 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein PVRIG level in Chronic kidney disease with hypertension and no diabetes (6464_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein PVRIG in blood serum http://purl.obolibrary.org/obo/OBA_2044648 GCST90238290 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein O-glucosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (6467_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein O-glucosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042150 GCST90238291 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tachykinin-4 level in Chronic kidney disease with hypertension and no diabetes (6468_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tachykinin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043764 GCST90238292 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte antigen 6 complex locus protein G6d level in Chronic kidney disease with hypertension and no diabetes (6469_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lymphocyte antigen 6 complex locus protein G6d in blood serum http://purl.obolibrary.org/obo/OBA_2042249 GCST90238293 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibulin-1 level in Chronic kidney disease with hypertension and no diabetes (6470_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibulin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041552 GCST90238294 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (6471_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement factor H-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0600091 GCST90238295 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanocyte protein PMEL level in Chronic kidney disease with hypertension and no diabetes (6472_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanocyte protein Pmel 17 in blood serum http://purl.obolibrary.org/obo/OBA_2043510 GCST90238296 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BPI fold-containing family A member 1 level in Chronic kidney disease with hypertension and no diabetes (6473_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BPI fold-containing family A member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042935 GCST90238297 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IgLON family member 5 level in Chronic kidney disease with hypertension and no diabetes (6478_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of IgLON family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044614 GCST90238298 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Soluble calcium-activated nucleotidase 1 level in Chronic kidney disease with hypertension and no diabetes (6480_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of soluble calcium-activated nucleotidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040886 GCST90238299 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Erythropoietin receptor level in Chronic kidney disease with hypertension and no diabetes (2715_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 erythropoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020364 GCST90237060 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulocyte colony-stimulating factor receptor level in Chronic kidney disease with hypertension and no diabetes (2719_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 granulocyte colony-stimulating factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020416 GCST90237061 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. fibromodulin level in Chronic kidney disease with hypertension and no diabetes (6367_66) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of fibromodulin in blood serum http://purl.obolibrary.org/obo/OBA_2041597 GCST90238227 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-like 1 level in Chronic kidney disease with hypertension and no diabetes (6368_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cystatin-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041178 GCST90238228 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deformed epidermal autoregulatory factor 1 homolog level in Chronic kidney disease with hypertension and no diabetes (6369_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deformed epidermal autoregulatory factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041261 GCST90238229 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-related protein 7 level in Chronic kidney disease with hypertension and no diabetes (6371_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of angiopoietin-related protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040589 GCST90238230 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Y-box-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (6372_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Y-box-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044160 GCST90238231 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein delta homolog 1 level in Chronic kidney disease with hypertension and no diabetes (6373_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein delta homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041313 GCST90238232 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-20 level in Chronic kidney disease with hypertension and no diabetes (6374_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of matrix metalloproteinase-20 in blood serum http://purl.obolibrary.org/obo/OBA_2042389 GCST90238233 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Xyloside xylosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (6375_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of xyloside xylosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044567 GCST90238234 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysozyme-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (6377_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lysozyme-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042253 GCST90238235 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein CEI level in Chronic kidney disease with hypertension and no diabetes (6378_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238236 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADAMTS-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (6379_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADAMTS-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040507 GCST90238237 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-tRNA hydrolase ICT1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (6380_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immature colon carcinoma transcript 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041968 GCST90238238 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-mannosidase level in Chronic kidney disease with hypertension and no diabetes (6382_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-mannosidase in blood serum http://purl.obolibrary.org/obo/OBA_2042279 GCST90238239 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tolloid-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (6383_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tolloid-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043864 GCST90238240 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 3 level in Chronic kidney disease with hypertension and no diabetes (6384_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WAP four-disulfide core domain protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044478 GCST90238241 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. von Willebrand factor A domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (6385_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of von Willebrand factor A domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044120 GCST90238242 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Defensin-5 level in Chronic kidney disease with hypertension and no diabetes (6387_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of defensin alpha 5 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044902 GCST90238243 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 126 level in Chronic kidney disease with hypertension and no diabetes (6388_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 126 in blood serum http://purl.obolibrary.org/obo/OBA_2044556 GCST90238244 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropeptide S level in Chronic kidney disease with hypertension and no diabetes (6390_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuropeptide S in blood serum http://purl.obolibrary.org/obo/OBA_2042620 GCST90238245 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily A member 3 level in Chronic kidney disease with hypertension and no diabetes (6391_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily A member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042196 GCST90238246 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WNT1-inducible-signaling pathway protein 2 level in Chronic kidney disease with hypertension and no diabetes (6392_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CCN family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044136 GCST90238247 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmin level in Chronic kidney disease with hypertension and no diabetes (6393_63) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of endoplasmin in blood serum http://purl.obolibrary.org/obo/OBA_2041945 GCST90238248 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycoprotein hormone alpha-2 level in Chronic kidney disease with hypertension and no diabetes (6395_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycoprotein hormone alpha-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041771 GCST90238249 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lon protease homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (6398_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Lon protease, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042218 GCST90238250 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 107 level in Chronic kidney disease with hypertension and no diabetes (6399_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 107 in blood serum http://purl.obolibrary.org/obo/OBA_2041269 GCST90238251 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor protein p53-inducible protein 13 level in Chronic kidney disease with hypertension and no diabetes (6400_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor protein p53-inducible protein 13 in blood serum http://purl.obolibrary.org/obo/OBA_2043905 GCST90238252 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paired immunoglobulin-like type 2 receptor alpha isoform FDF03-deltaTM level in Chronic kidney disease with hypertension and no diabetes (6402_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of paired immunoglobulin-like type 2 receptor alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042892 GCST90238253 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C1q-related factor level in Chronic kidney disease with hypertension and no diabetes (6404_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C1q-related factor in blood serum http://purl.obolibrary.org/obo/OBA_2040845 GCST90238254 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 2 level in Chronic kidney disease with hypertension and no diabetes (6405_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pregnancy-specific beta-1-glycoprotein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043057 GCST90238255 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Normal mucosa of esophagus-specific gene 1 protein level in Chronic kidney disease with hypertension and no diabetes (6406_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of normal mucosa of esophagus-specific gene 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042597 GCST90238256 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ladinin-1 level in Chronic kidney disease with hypertension and no diabetes (6407_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ladinin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042155 GCST90238257 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin beta C chain level in Chronic kidney disease with hypertension and no diabetes (6408_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activin/inhibin beta C chain in blood serum http://purl.obolibrary.org/obo/OBA_2040211 GCST90238258 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G protein-coupled receptor F5 level in Chronic kidney disease with hypertension and no diabetes (6409_57) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of adhesion G protein-coupled receptor F5 in blood serum http://purl.obolibrary.org/obo/OBA_2044609 GCST90238259 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Early placenta insulin-like peptide level in Chronic kidney disease with hypertension and no diabetes (6410_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of early placenta insulin-like peptide in blood serum http://purl.obolibrary.org/obo/OBA_2042035 GCST90238260 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 135 level in Chronic kidney disease with hypertension and no diabetes (6411_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 135 in blood serum http://purl.obolibrary.org/obo/OBA_2041284 GCST90238261 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lipase member K level in Chronic kidney disease with hypertension and no diabetes (6413_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lipase member K in blood serum http://purl.obolibrary.org/obo/OBA_2042208 GCST90238262 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Out at first protein homolog level in Chronic kidney disease with hypertension and no diabetes (6414_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of out at first protein in blood serum http://purl.obolibrary.org/obo/OBA_2042685 GCST90238263 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase N subunit 2 level in Chronic kidney disease with hypertension and no diabetes (6415_90) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of carboxypeptidase N subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041122 GCST90238264 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastrokine-2 level in Chronic kidney disease with hypertension and no diabetes (6416_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gastrokine-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041725 GCST90238265 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-16 level in Chronic kidney disease with hypertension and no diabetes (6421_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-16 in blood serum http://purl.obolibrary.org/obo/OBA_2041977 GCST90238266 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (6423_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040846 GCST90238267 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable inactive ribonuclease-like protein 13 level in Chronic kidney disease with hypertension and no diabetes (6424_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonuclease-like protein 13 in blood serum http://purl.obolibrary.org/obo/OBA_2043282 GCST90238268 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-19 level in Chronic kidney disease with hypertension and no diabetes (6425_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of matrix metalloproteinase-19 in blood serum http://purl.obolibrary.org/obo/OBA_2042388 GCST90238269 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM19A2 level in Chronic kidney disease with hypertension and no diabetes (6430_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chemokine-like protein TAFA-2 in blood serum http://purl.obolibrary.org/obo/OBA_2044477 GCST90238270 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prenylcysteine oxidase 1 level in Chronic kidney disease with hypertension and no diabetes (6431_68) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prenylcysteine oxidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044577 GCST90238271 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pseudokinase FAM20A level in Chronic kidney disease with hypertension and no diabetes (6433_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pseudokinase FAM20A in blood serum http://purl.obolibrary.org/obo/OBA_2044615 GCST90238272 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retina-specific copper amine oxidase level in Chronic kidney disease with hypertension and no diabetes (6434_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retina-specific copper amine oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2040605 GCST90238273 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microfibrillar-associated protein 5 level in Chronic kidney disease with hypertension and no diabetes (6440_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microfibrillar-associated protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042352 GCST90238274 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ferritin heavy chain level in Chronic kidney disease with hypertension and no diabetes (25913_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ferritin heavy chain in blood serum http://purl.obolibrary.org/obo/OBA_2041624 GCST90236985 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-hexosaminidase alpha chain level in Chronic kidney disease with hypertension and no diabetes (25917_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-hexosaminidase subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041864 GCST90236986 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HLA class I histocompatibility antigen, alpha chain E level in Chronic kidney disease with hypertension and no diabetes (25918_60) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MHC class I histocompatibility antigen, alpha chain E in blood serum http://purl.obolibrary.org/obo/OBA_2041881 GCST90236987 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin a subunit level in Chronic kidney disease with hypertension and no diabetes (25921_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inhibin alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040319 GCST90236988 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 5 level in Chronic kidney disease with hypertension and no diabetes (25922_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor-related protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042234 GCST90236989 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (25926_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LIM domain-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042179 GCST90236990 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurogenin-3 level in Chronic kidney disease with hypertension and no diabetes (25938_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurogenin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042567 GCST90236991 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 3-kinase catalytic subunit type 3 level in Chronic kidney disease with hypertension and no diabetes (25947_116) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol 3-kinase catalytic subunit type 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042889 GCST90236992 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase N2 level in Chronic kidney disease with hypertension and no diabetes (25948_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase N2 in blood serum http://purl.obolibrary.org/obo/OBA_2042908 GCST90236993 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3 level in Chronic kidney disease with hypertension and no diabetes (25949_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042920 GCST90236994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Preferentially expressed antigen of melanoma level in Chronic kidney disease with hypertension and no diabetes (25951_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of melanoma antigen preferentially expressed in tumors in blood serum http://purl.obolibrary.org/obo/OBA_2043016 GCST90236995 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-type tyrosine-protein phosphatase-like N level in Chronic kidney disease with hypertension and no diabetes (25954_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-type tyrosine-protein phosphatase-like N in blood serum http://purl.obolibrary.org/obo/OBA_2043107 GCST90236996 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rap guanine nucleotide exchange factor 1 level in Chronic kidney disease with hypertension and no diabetes (25956_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rap guanine nucleotide exchange factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043196 GCST90236997 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sex-determining region Y protein level in Chronic kidney disease with hypertension and no diabetes (25957_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sex-determining region Y protein in blood serum http://purl.obolibrary.org/obo/OBA_2043662 GCST90236998 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plastin-3 level in Chronic kidney disease with hypertension and no diabetes (25960_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plastin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042932 GCST90236999 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase WNK1 level in Chronic kidney disease with hypertension and no diabetes (25962_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase WNK1 in blood serum http://purl.obolibrary.org/obo/OBA_2044137 GCST90237000 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Exportin-5 level in Chronic kidney disease with hypertension and no diabetes (25963_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of exportin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2044151 GCST90237001 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q tumor necrosis factor-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (25964_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q tumor necrosis factor-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040851 GCST90237002 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metalloproteinase inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (25967_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 metalloproteinase inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020566 GCST90237003 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor A level in Chronic kidney disease with hypertension and no diabetes (2597_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 vascular endothelial growth factor A measurement http://www.ebi.ac.uk/efo/EFO_0010804 GCST90237004 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 9 level in Chronic kidney disease with hypertension and no diabetes (2598_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90237005 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 9 level in Chronic kidney disease with hypertension and no diabetes (2599_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0020798 GCST90237006 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-2 level in Chronic kidney disease with hypertension and no diabetes (2602_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90237007 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-lymphocyte activation antigen CD80 level in Chronic kidney disease with hypertension and no diabetes (2603_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 t-lymphocyte activation antigen CD80 measurement http://www.ebi.ac.uk/efo/EFO_0020761 GCST90237008 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 8 level in Chronic kidney disease with hypertension and no diabetes (2605_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0020816 GCST90237009 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Reticulon-4 receptor-like 1 level in Chronic kidney disease with hypertension and no diabetes (20546_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of reticulon-4 receptor-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043354 GCST90235467 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal acetylcholine receptor subunit beta-3 level in Chronic kidney disease with hypertension and no diabetes (20547_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuronal acetylcholine receptor subunit beta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041018 GCST90235468 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Izumo sperm-egg fusion protein 4 level in Chronic kidney disease with hypertension and no diabetes (20549_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of izumo sperm-egg fusion protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044625 GCST90235469 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurotrimin level in Chronic kidney disease with hypertension and no diabetes (20550_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurotrimin in blood serum http://purl.obolibrary.org/obo/OBA_2042654 GCST90235470 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoinositide-3-kinase-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (20553_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoinositide-3-kinase-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042890 GCST90235471 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and immunoglobulin domain-containing protein 8 level in Chronic kidney disease with hypertension and no diabetes (20557_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-set and immunoglobulin domain-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044440 GCST90235472 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 8 level in Chronic kidney disease with hypertension and no diabetes (20558_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ephrin type-A receptor 8 in blood serum http://purl.obolibrary.org/obo/OBA_2041492 GCST90235473 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-6 level in Chronic kidney disease with hypertension and no diabetes (20561_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of contactin-6 in blood serum http://purl.obolibrary.org/obo/OBA_2041074 GCST90235474 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell lectin-like receptor subfamily B member 1 level in Chronic kidney disease with hypertension and no diabetes (20562_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of killer cell lectin-like receptor subfamily B member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044226 GCST90235475 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 10 level in Chronic kidney disease with hypertension and no diabetes (20563_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Toll-like receptor 10 in blood serum http://purl.obolibrary.org/obo/OBA_2040249 GCST90235476 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thy-1 membrane glycoprotein level in Chronic kidney disease with hypertension and no diabetes (20564_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Thy-1 membrane glycoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2040337 GCST90235477 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FRAS1-related extracellular matrix protein 1 level in Chronic kidney disease with hypertension and no diabetes (20568_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of FRAS1-related extracellular matrix protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041615 GCST90235478 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and transmembrane domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (20570_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of V-set and transmembrane domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044452 GCST90235479 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 9 member A level in Chronic kidney disease with hypertension and no diabetes (20575_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 9 member A in blood serum http://purl.obolibrary.org/obo/OBA_2044233 GCST90235480 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-7 level in Chronic kidney disease with hypertension and no diabetes (20576_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frizzled-7 in blood serum http://purl.obolibrary.org/obo/OBA_2041642 GCST90235481 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-8 level in Chronic kidney disease with hypertension and no diabetes (20577_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frizzled-8 in blood serum http://purl.obolibrary.org/obo/OBA_2041643 GCST90235482 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Latrophilin-3 level in Chronic kidney disease with hypertension and no diabetes (20578_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of adhesion G protein-coupled receptor L3 in blood serum http://purl.obolibrary.org/obo/OBA_2040253 GCST90235483 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myelin-associated glycoprotein level in Chronic kidney disease with hypertension and no diabetes (20579_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myelin-associated glycoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2042263 GCST90235484 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nectin-1, isoform gamma level in Chronic kidney disease with hypertension and no diabetes (20584_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235485 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 9 level in Chronic kidney disease with hypertension and no diabetes (20585_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMRF35-like molecule 9 in blood serum http://purl.obolibrary.org/obo/OBA_2040944 GCST90235486 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 9 level in Chronic kidney disease with hypertension and no diabetes (20585_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMRF35-like molecule 9 in blood serum http://purl.obolibrary.org/obo/OBA_2040944 GCST90235487 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-3 level in Chronic kidney disease with hypertension and no diabetes (20586_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of contactin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041073 GCST90235488 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-4 level in Chronic kidney disease with hypertension and no diabetes (20589_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040963 GCST90235489 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropeptide Y level in Chronic kidney disease with hypertension and no diabetes (20590_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuropeptide Y in blood serum http://purl.obolibrary.org/obo/OBA_2042625 GCST90235490 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gliomedin level in Chronic kidney disease with hypertension and no diabetes (20591_48) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of gliomedin in blood serum http://purl.obolibrary.org/obo/OBA_2041728 GCST90235491 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 3 level in Chronic kidney disease with hypertension and no diabetes (2649_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 intercellular adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020482 GCST90237035 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urokinase plasminogen activator surface receptor level in Chronic kidney disease with hypertension and no diabetes (2652_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 urokinase plasminogen activator surface receptor measurement http://www.ebi.ac.uk/efo/EFO_0010932 GCST90237036 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 1A level in Chronic kidney disease with hypertension and no diabetes (2654_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor necrosis factor receptor superfamily member 1A in blood serum http://purl.obolibrary.org/obo/OBA_2040361 GCST90237037 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NT-3 growth factor receptor level in Chronic kidney disease with hypertension and no diabetes (2658_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 nt-3 growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020613 GCST90237038 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 17 level in Chronic kidney disease with hypertension and no diabetes (2665_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 17 measurement http://www.ebi.ac.uk/efo/EFO_0020806 GCST90237039 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Decorin level in Chronic kidney disease with hypertension and no diabetes (2666_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 decorin measurement http://www.ebi.ac.uk/efo/EFO_0020315 GCST90237040 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpain I level in Chronic kidney disease with hypertension and no diabetes (2668_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 calpain I measurement http://www.ebi.ac.uk/efo/EFO_0008064 GCST90237041 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Creatine kinase M-type level in Chronic kidney disease with hypertension and no diabetes (2670_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 creatine kinase m-type measurement http://www.ebi.ac.uk/efo/EFO_0020291 GCST90237042 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor receptor level in Chronic kidney disease with hypertension and no diabetes (2677_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 epidermal growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020359 GCST90237043 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte growth factor level in Chronic kidney disease with hypertension and no diabetes (2681_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 hepatocyte growth factor measurement http://www.ebi.ac.uk/efo/EFO_0006903 GCST90237044 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C3b, inactivated level in Chronic kidney disease with hypertension and no diabetes (2683_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C3B, inactivated measurement http://www.ebi.ac.uk/efo/EFO_0020276 GCST90237045 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 5 level in Chronic kidney disease with hypertension and no diabetes (2685_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020477 GCST90237046 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 6 level in Chronic kidney disease with hypertension and no diabetes (2686_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020478 GCST90237047 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-derived growth regulatory protein level in Chronic kidney disease with hypertension and no diabetes (2687_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 melanoma-derived growth regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0008229 GCST90237048 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipase A2, membrane associated level in Chronic kidney disease with hypertension and no diabetes (2692_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 phospholipase A2, membrane associated measurement http://www.ebi.ac.uk/efo/EFO_0008259 GCST90237049 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oncostatin-M level in Chronic kidney disease with hypertension and no diabetes (2693_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90237050 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet endothelial cell adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (2695_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet endothelial cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0010598 GCST90237051 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Persephin level in Chronic kidney disease with hypertension and no diabetes (2696_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 persephin measurement http://www.ebi.ac.uk/efo/EFO_0020632 GCST90237052 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitamin K-dependent protein S level in Chronic kidney disease with hypertension and no diabetes (2700_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 vitamin k-dependent protein S measurement http://www.ebi.ac.uk/efo/EFO_0020850 GCST90237053 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 13B level in Chronic kidney disease with hypertension and no diabetes (2704_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020803 GCST90237054 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 25 level in Chronic kidney disease with hypertension and no diabetes (2705_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90237055 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyroxine-binding globulin level in Chronic kidney disease with hypertension and no diabetes (2706_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 thyroxine-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0009172 GCST90237056 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 18 level in Chronic kidney disease with hypertension and no diabetes (2708_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 tumor necrosis factor ligand superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020795 GCST90237057 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ciliary neurotrophic factor receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (2711_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 ciliary neurotrophic factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020261 GCST90237058 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelial monocyte-activating polypeptide 2 level in Chronic kidney disease with hypertension and no diabetes (2714_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 endothelial monocyte-activating polypeptide 2 measurement http://www.ebi.ac.uk/efo/EFO_0020348 GCST90237059 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine receptor-like factor 1:Cardiotrophin-like cytokine factor 1 Complex level in Chronic kidney disease with hypertension and no diabetes (2607_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytokine receptor-like factor 1:cardiotrophin-like cytokine factor 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020305 GCST90237010 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-C level in Chronic kidney disease with hypertension and no diabetes (2609_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin C measurement http://www.ebi.ac.uk/efo/EFO_0004617 GCST90237011 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase receptor TYRO3 level in Chronic kidney disease with hypertension and no diabetes (2611_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase receptor TYRO3 measurement http://www.ebi.ac.uk/efo/EFO_0020829 GCST90237012 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 5 level in Chronic kidney disease with hypertension and no diabetes (2612_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 eukaryotic translation initiation factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020369 GCST90237013 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A4 level in Chronic kidney disease with hypertension and no diabetes (2614_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A4 measurement http://www.ebi.ac.uk/efo/EFO_0020356 GCST90237014 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A5 level in Chronic kidney disease with hypertension and no diabetes (2615_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A5 measurement http://www.ebi.ac.uk/efo/EFO_0020357 GCST90237015 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor tyrosine-protein kinase erbB-2 level in Chronic kidney disease with hypertension and no diabetes (2616_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 receptor tyrosine-protein kinase erbb-2 measurement http://www.ebi.ac.uk/efo/EFO_0020700 GCST90237016 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor tyrosine-protein kinase erbB-3 level in Chronic kidney disease with hypertension and no diabetes (2617_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 receptor tyrosine-protein kinase erbb-3 measurement http://www.ebi.ac.uk/efo/EFO_0020701 GCST90237017 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor tyrosine-protein kinase erbB-4 level in Chronic kidney disease with hypertension and no diabetes (2618_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 receptor tyrosine-protein kinase erbb-4 measurement http://www.ebi.ac.uk/efo/EFO_0020702 GCST90237018 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor-associated calcium signal transducer 2 level in Chronic kidney disease with hypertension and no diabetes (2619_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor-associated calcium signal transducer 2 measurement http://www.ebi.ac.uk/efo/EFO_0020817 GCST90237019 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-6 receptor subunit beta level in Chronic kidney disease with hypertension and no diabetes (2620_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-6 receptor subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040342 GCST90237020 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heme oxygenase 2 level in Chronic kidney disease with hypertension and no diabetes (2622_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 heme oxygenase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020436 GCST90237021 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hsp90alpha level in Chronic kidney disease with hypertension and no diabetes (2625_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock protein HSP 90-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041944 GCST90237022 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 Receptor accessory protein level in Chronic kidney disease with hypertension and no diabetes (2630_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-1 receptor accessory protein in blood serum http://purl.obolibrary.org/obo/OBA_2042008 GCST90237023 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-12 receptor subunit beta-1 level in Chronic kidney disease with hypertension and no diabetes (2632_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90237024 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine receptor common subunit gamma level in Chronic kidney disease with hypertension and no diabetes (2634_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytokine receptor common subunit gamma measurement http://www.ebi.ac.uk/efo/EFO_0020304 GCST90237025 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Layilin level in Chronic kidney disease with hypertension and no diabetes (2635_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 layilin measurement http://www.ebi.ac.uk/efo/EFO_0020529 GCST90237026 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage mannose receptor 1 level in Chronic kidney disease with hypertension and no diabetes (2637_77) 466 African American individuals NA Illumina [14870897] (imputed) 1 macrophage mannose receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020548 GCST90237027 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage colony-stimulating factor 1 receptor level in Chronic kidney disease with hypertension and no diabetes (2638_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage colony-stimulating factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020547 GCST90237028 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage-stimulating protein receptor level in Chronic kidney disease with hypertension and no diabetes (2640_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage-stimulating protein receptor measurement http://www.ebi.ac.uk/efo/EFO_0020550 GCST90237029 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-activating factor acetylhydrolase IB subunit beta level in Chronic kidney disease with hypertension and no diabetes (2642_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet-activating factor acetylhydrolase ib subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020646 GCST90237030 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-3 level in Chronic kidney disease with hypertension and no diabetes (2643_57) 466 African American individuals NA Illumina [14870897] (imputed) 1 cadherin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020213 GCST90237031 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C alpha type level in Chronic kidney disease with hypertension and no diabetes (2644_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein kinase c alpha type measurement http://www.ebi.ac.uk/efo/EFO_0020677 GCST90237032 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C zeta type level in Chronic kidney disease with hypertension and no diabetes (2645_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein kinase c zeta type measurement http://www.ebi.ac.uk/efo/EFO_0020683 GCST90237033 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab GDP dissociation inhibitor beta level in Chronic kidney disease with hypertension and no diabetes (2647_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 rab gdp dissociation inhibitor beta measurement http://www.ebi.ac.uk/efo/EFO_0020697 GCST90237034 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like modifier-activating enzyme 5 level in Chronic kidney disease with hypertension and no diabetes (21314_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like modifier-activating enzyme 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043982 GCST90235662 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NF-kappa-B inhibitor-interacting Ras-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (21317_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NF-kappa-B inhibitor-interacting Ras-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042586 GCST90235663 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. rRNA methyltransferase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21319_196) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of rRNA methyltransferase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042420 GCST90235664 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U2 small nuclear ribonucleoprotein AAE level in Chronic kidney disease with hypertension and no diabetes (21321_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235665 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription initiation factor IIE subunit beta level in Chronic kidney disease with hypertension and no diabetes (21322_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription initiation factor IIE subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2044363 GCST90235666 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RWD domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (21323_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RWD domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043358 GCST90235667 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin-specific chaperone C level in Chronic kidney disease with hypertension and no diabetes (21326_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin-specific chaperone C in blood serum http://purl.obolibrary.org/obo/OBA_2043791 GCST90235668 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Modulator of retrovirus infection homolog level in Chronic kidney disease with hypertension and no diabetes (21327_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of modulator of retrovirus infection in blood serum http://purl.obolibrary.org/obo/OBA_2042417 GCST90235669 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-1 level in Chronic kidney disease with hypertension and no diabetes (21328_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043748 GCST90235670 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyridoxal phosphate phosphatase PHOSPHO2 level in Chronic kidney disease with hypertension and no diabetes (21329_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyridoxal phosphate phosphatase PHOSPHO2 in blood serum http://purl.obolibrary.org/obo/OBA_2042878 GCST90235671 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosyl-tRNA synthetase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21330_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine--tRNA ligase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044158 GCST90235672 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell CLL/lymphoma 7 protein family member A level in Chronic kidney disease with hypertension and no diabetes (21331_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell CLL/lymphoma 7 protein family member A in blood serum http://purl.obolibrary.org/obo/OBA_2044255 GCST90235673 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleotide exchange factor SIL1 level in Chronic kidney disease with hypertension and no diabetes (21338_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleotide exchange factor SIL1 in blood serum http://purl.obolibrary.org/obo/OBA_2043509 GCST90235674 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alanine aminotransferase 2 level in Chronic kidney disease with hypertension and no diabetes (21339_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alanine aminotransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041777 GCST90235675 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatic leukemia factor level in Chronic kidney disease with hypertension and no diabetes (21340_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatic leukemia factor in blood serum http://purl.obolibrary.org/obo/OBA_2041883 GCST90235676 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Charged multivesicular body protein 4a level in Chronic kidney disease with hypertension and no diabetes (21341_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of charged multivesicular body protein 4a in blood serum http://purl.obolibrary.org/obo/OBA_2041012 GCST90235677 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 14 level in Chronic kidney disease with hypertension and no diabetes (21342_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 14 in blood serum http://purl.obolibrary.org/obo/OBA_2043255 GCST90235678 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activity-regulated cytoskeleton-associated protein level in Chronic kidney disease with hypertension and no diabetes (21343_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activity-regulated cytoskeleton-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2040637 GCST90235679 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dimethyladenosine transferase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21344_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dimethyladenosine transferase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043831 GCST90235680 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol dehydrogenase 12 level in Chronic kidney disease with hypertension and no diabetes (21345_93) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of retinol dehydrogenase 12 in blood serum http://purl.obolibrary.org/obo/OBA_2043225 GCST90235681 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydroorotate dehydrogenase (quinone), mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21346_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydroorotate dehydrogenase (quinone), mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041294 GCST90235682 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA 2'-phosphotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (21348_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA 2'-phosphotransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043943 GCST90235683 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine/tyrosine-interacting protein level in Chronic kidney disease with hypertension and no diabetes (21349_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine/threonine/tyrosine-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043721 GCST90235684 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein lin-28 homolog B level in Chronic kidney disease with hypertension and no diabetes (21350_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein lin-28 homolog B in blood serum http://purl.obolibrary.org/obo/OBA_2042204 GCST90235685 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycyl t-RNA synthetase level in Chronic kidney disease with hypertension and no diabetes (21351_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycine--tRNA ligase in blood serum http://purl.obolibrary.org/obo/OBA_2041672 GCST90235686 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uracil phosphoribosyltransferase homolog level in Chronic kidney disease with hypertension and no diabetes (21354_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uracil phosphoribosyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044044 GCST90235687 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Upstream stimulatory factor 1 level in Chronic kidney disease with hypertension and no diabetes (21355_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of upstream stimulatory factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044048 GCST90235688 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B9 domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (21356_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B9 domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040762 GCST90235689 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal regeneration-related protein level in Chronic kidney disease with hypertension and no diabetes (21359_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuronal regeneration-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2044499 GCST90235690 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm antigen with calponin homology and coiled-coil domains 1 level in Chronic kidney disease with hypertension and no diabetes (21360_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cytospin-B in blood serum http://purl.obolibrary.org/obo/OBA_2044276 GCST90235691 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein TXNRD3NB level in Chronic kidney disease with hypertension and no diabetes (21361_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative uncharacterized protein TXNRD3NB in blood serum http://purl.obolibrary.org/obo/OBA_2044443 GCST90235692 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytohesin-3 level in Chronic kidney disease with hypertension and no diabetes (21365_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytohesin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041219 GCST90235693 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein Musashi homolog 2 level in Chronic kidney disease with hypertension and no diabetes (21366_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein Musashi homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042440 GCST90235694 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor-binding factor 2 level in Chronic kidney disease with hypertension and no diabetes (21367_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor-binding factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042635 GCST90235695 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spindle and kinetochore-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (21370_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spindle and kinetochore-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043518 GCST90235696 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional lysine-specific demethylase and histidyl-hydroxylase MINA level in Chronic kidney disease with hypertension and no diabetes (21371_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosomal oxygenase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044331 GCST90235697 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Queuine tRNA-ribosyltransferase subunit QTRTD1 level in Chronic kidney disease with hypertension and no diabetes (21373_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of queuine tRNA-ribosyltransferase accessory subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044349 GCST90235698 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide exchange factor for Rab-3A level in Chronic kidney disease with hypertension and no diabetes (21375_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide exchange factor for Rab-3A in blood serum http://purl.obolibrary.org/obo/OBA_2043162 GCST90235699 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyribonucleotide nucleotidyltransferase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21378_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyribonucleotide nucleotidyltransferase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042956 GCST90235700 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ethanolamine kinase 2 level in Chronic kidney disease with hypertension and no diabetes (21379_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ethanolamine kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041516 GCST90235701 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Queuine tRNA-ribosyltransferase level in Chronic kidney disease with hypertension and no diabetes (21380_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of queuine tRNA-ribosyltransferase catalytic subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043137 GCST90235702 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TBC1 domain family member 22B level in Chronic kidney disease with hypertension and no diabetes (21381_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TBC1 domain family member 22B in blood serum http://purl.obolibrary.org/obo/OBA_2043785 GCST90235703 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc phosphodiesterase ELAC protein 1 level in Chronic kidney disease with hypertension and no diabetes (21382_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc phosphodiesterase ELAC protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041462 GCST90235704 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Asparaginyl-tRNA synthetase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (21383_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of asparagine--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2042513 GCST90235705 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-L-fucoside fucohydrolase level in Chronic kidney disease with hypertension and no diabetes (21384_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tissue alpha-L-fucosidase in blood serum http://purl.obolibrary.org/obo/OBA_2041631 GCST90235706 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT and NTRK-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (21385_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLIT and NTRK-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043547 GCST90235707 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Meprin A subunit alpha level in Chronic kidney disease with hypertension and no diabetes (21387_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of meprin A subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042339 GCST90235708 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. L-dopachrome tautomerase level in Chronic kidney disease with hypertension and no diabetes (21390_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of L-dopachrome tautomerase in blood serum http://purl.obolibrary.org/obo/OBA_2041244 GCST90235709 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Choriogonadotropin subunit beta 3 level in Chronic kidney disease with hypertension and no diabetes (21391_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of choriogonadotropin subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040995 GCST90235710 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin-17 level in Chronic kidney disease with hypertension and no diabetes (21395_23) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protocadherin-17 in blood serum http://purl.obolibrary.org/obo/OBA_2042781 GCST90235711 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane emp24 domain-containing protein 9 level in Chronic kidney disease with hypertension and no diabetes (21236_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transmembrane emp24 domain-containing protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2044630 GCST90235637 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-arginine deiminase type-4 level in Chronic kidney disease with hypertension and no diabetes (21237_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-arginine deiminase type-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042742 GCST90235638 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CDK5 regulatory subunit-associated protein 3 level in Chronic kidney disease with hypertension and no diabetes (21238_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CDK5 regulatory subunit-associated protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040968 GCST90235639 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytohesin-1 level in Chronic kidney disease with hypertension and no diabetes (21239_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytohesin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041217 GCST90235640 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aminomethyltransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21240_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aminomethyltransferase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040584 GCST90235641 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetyltransferase 6 level in Chronic kidney disease with hypertension and no diabetes (21241_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-alpha-acetyltransferase 80 in blood serum http://purl.obolibrary.org/obo/OBA_2042518 GCST90235642 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleophosmin level in Chronic kidney disease with hypertension and no diabetes (21244_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleophosmin in blood serum http://purl.obolibrary.org/obo/OBA_2042616 GCST90235643 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-adenosylmethionine synthase isoform type-1 level in Chronic kidney disease with hypertension and no diabetes (21247_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of S-adenosylmethionine synthetase isoform type-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042304 GCST90235644 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA fragmentation factor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (21249_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA fragmentation factor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040398 GCST90235645 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 16 level in Chronic kidney disease with hypertension and no diabetes (21255_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 16 in blood serum http://purl.obolibrary.org/obo/OBA_2043256 GCST90235646 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small nuclear ribonucleoprotein E level in Chronic kidney disease with hypertension and no diabetes (21260_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small nuclear ribonucleoprotein E in blood serum http://purl.obolibrary.org/obo/OBA_2043577 GCST90235647 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epoxide hydrolase 2 level in Chronic kidney disease with hypertension and no diabetes (21269_198) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epoxide hydrolase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041495 GCST90235648 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldo-keto reductase family 1 member C2 level in Chronic kidney disease with hypertension and no diabetes (21271_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member C2 in blood serum http://purl.obolibrary.org/obo/OBA_2040550 GCST90235649 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0568 protein C14orf166 level in Chronic kidney disease with hypertension and no diabetes (21272_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein C14orf166 in blood serum http://purl.obolibrary.org/obo/OBA_2044800 GCST90235650 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD133 antigen level in Chronic kidney disease with hypertension and no diabetes (21276_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prominin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040326 GCST90235651 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TSC22 domain family protein 3 level in Chronic kidney disease with hypertension and no diabetes (21280_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TSC22 domain family protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043944 GCST90235652 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase II inhibitor 2 level in Chronic kidney disease with hypertension and no diabetes (21281_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium/calmodulin-dependent protein kinase II inhibitor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040882 GCST90235653 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TNFAIP3-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (21282_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TNFAIP3-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043890 GCST90235654 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S ribosomal protein L11 level in Chronic kidney disease with hypertension and no diabetes (21286_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S ribosomal protein L11 in blood serum http://purl.obolibrary.org/obo/OBA_2043318 GCST90235655 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm-associated antigen 7 level in Chronic kidney disease with hypertension and no diabetes (21289_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm-associated antigen 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043613 GCST90235656 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Checkpoint protein HUS1 level in Chronic kidney disease with hypertension and no diabetes (21290_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of checkpoint protein HUS1 in blood serum http://purl.obolibrary.org/obo/OBA_2041960 GCST90235657 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HAUS augmin-like complex subunit 1 level in Chronic kidney disease with hypertension and no diabetes (21306_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of HAUS augmin-like complex subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040927 GCST90235658 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dehydrogenase/reductase SDR family member 4 level in Chronic kidney disease with hypertension and no diabetes (21308_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dehydrogenase/reductase SDR family member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041296 GCST90235659 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. mRNA turnover protein 4 homolog level in Chronic kidney disease with hypertension and no diabetes (21310_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mRNA turnover protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042436 GCST90235660 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Jun dimerization protein 2 level in Chronic kidney disease with hypertension and no diabetes (21311_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Jun dimerization protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042070 GCST90235661 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromodomain-helicase-DNA-binding protein 7 level in Chronic kidney disease with hypertension and no diabetes (14005_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromodomain-helicase-DNA-binding protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041002 GCST90234123 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycine N-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (14006_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycine N-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041755 GCST90234124 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1 level in Chronic kidney disease with hypertension and no diabetes (14007_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042761 GCST90234125 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. mRNA-decapping enzyme 1A level in Chronic kidney disease with hypertension and no diabetes (14008_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mRNA-decapping enzyme 1A in blood serum http://purl.obolibrary.org/obo/OBA_2041242 GCST90234126 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor alpha-induced protein 3 level in Chronic kidney disease with hypertension and no diabetes (14009_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor necrosis factor alpha-induced protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043888 GCST90234127 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A11 level in Chronic kidney disease with hypertension and no diabetes (14011_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A11 in blood serum http://purl.obolibrary.org/obo/OBA_2043363 GCST90234128 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable ATP-dependent RNA helicase DHX58 level in Chronic kidney disease with hypertension and no diabetes (14012_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent RNA helicase DHX58 in blood serum http://purl.obolibrary.org/obo/OBA_2044785 GCST90234129 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TRAF family member-associated NF-kappa-B activator level in Chronic kidney disease with hypertension and no diabetes (14013_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TRAF family member-associated NF-kappa-B activator in blood serum http://purl.obolibrary.org/obo/OBA_2040418 GCST90234130 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Envoplakin level in Chronic kidney disease with hypertension and no diabetes (14019_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of envoplakin in blood serum http://purl.obolibrary.org/obo/OBA_2041522 GCST90234131 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mediator of RNA polymerase II transcription subunit 4 level in Chronic kidney disease with hypertension and no diabetes (14021_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mediator of RNA polymerase II transcription subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042329 GCST90234132 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17B level in Chronic kidney disease with hypertension and no diabetes (14022_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17B measurement http://www.ebi.ac.uk/efo/EFO_0021973 GCST90234133 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectodysplasin-A, secreted form level in Chronic kidney disease with hypertension and no diabetes (14024_196) 466 African American individuals NA Illumina [14870897] (imputed) 0 ectodysplasin-a, secreted form measurement http://www.ebi.ac.uk/efo/EFO_0020341 GCST90234134 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 9 level in Chronic kidney disease with hypertension and no diabetes (14025_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 9 measurement http://www.ebi.ac.uk/efo/EFO_0010802 GCST90234135 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17F level in Chronic kidney disease with hypertension and no diabetes (14026_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17F measurement http://www.ebi.ac.uk/efo/EFO_0021963 GCST90234136 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha level in Chronic kidney disease with hypertension and no diabetes (14028_22) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042888 GCST90234137 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COP9 signalosome complex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (14029_42) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of COP9 signalosome complex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041096 GCST90234138 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 4 level in Chronic kidney disease with hypertension and no diabetes (14030_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90234139 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 7 level in Chronic kidney disease with hypertension and no diabetes (14031_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90234140 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor A, isoform 121 level in Chronic kidney disease with hypertension and no diabetes (14032_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 vascular endothelial growth factor A, isoform 121 measurement http://www.ebi.ac.uk/efo/EFO_0020847 GCST90234141 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor-associated calcium signal transducer 2 level in Chronic kidney disease with hypertension and no diabetes (14034_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor-associated calcium signal transducer 2 measurement http://www.ebi.ac.uk/efo/EFO_0020817 GCST90234142 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-lymphoma invasion and metastasis-inducing protein 1 level in Chronic kidney disease with hypertension and no diabetes (14035_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho guanine nucleotide exchange factor TIAM1 in blood serum http://purl.obolibrary.org/obo/OBA_2043848 GCST90234143 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Multiple PDZ domain protein level in Chronic kidney disease with hypertension and no diabetes (14036_116) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of multiple PDZ domain protein in blood serum http://purl.obolibrary.org/obo/OBA_2042403 GCST90234144 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ran-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (14037_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ran-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043191 GCST90234145 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-5 level in Chronic kidney disease with hypertension and no diabetes (14039_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90234146 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granzyme B level in Chronic kidney disease with hypertension and no diabetes (14041_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 granzyme b measurement http://www.ebi.ac.uk/efo/EFO_0020418 GCST90234147 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphotactin level in Chronic kidney disease with hypertension and no diabetes (14078_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphotactin measurement http://www.ebi.ac.uk/efo/EFO_0008214 GCST90234173 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-18 receptor 1 level in Chronic kidney disease with hypertension and no diabetes (14079_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin 18 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008178 GCST90234174 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2D ligand 1 level in Chronic kidney disease with hypertension and no diabetes (14081_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 NKG2-D ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020609 GCST90234175 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Talin-2 level in Chronic kidney disease with hypertension and no diabetes (14082_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of talin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043865 GCST90234176 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Selenide, water dikinase 1 level in Chronic kidney disease with hypertension and no diabetes (14083_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of selenide, water dikinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043444 GCST90234177 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-13 level in Chronic kidney disease with hypertension and no diabetes (14085_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-13 in blood serum http://purl.obolibrary.org/obo/OBA_2040280 GCST90234178 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acid sphingomyelinase-like phosphodiesterase 3a level in Chronic kidney disease with hypertension and no diabetes (14086_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90234179 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dimethyladenosine transferase 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21193_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dimethyladenosine transferase 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043832 GCST90235619 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SAM domain-containing protein SAMSN-1 level in Chronic kidney disease with hypertension and no diabetes (21196_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SAM domain-containing protein SAMSN-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044357 GCST90235620 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MORF4 family-associated protein 1-like 1 level in Chronic kidney disease with hypertension and no diabetes (21203_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MORF4 family-associated protein 1-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044668 GCST90235621 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desumoylating isopeptidase 1 level in Chronic kidney disease with hypertension and no diabetes (21204_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of desumoylating isopeptidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044280 GCST90235622 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HCLS1-associated protein X-1 level in Chronic kidney disease with hypertension and no diabetes (21206_218) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of HCLS1-associated protein X-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041839 GCST90235623 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional coenzyme A synthase level in Chronic kidney disease with hypertension and no diabetes (21207_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional coenzyme A synthase in blood serum http://purl.obolibrary.org/obo/OBA_2041077 GCST90235624 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CCAAT/enhancer-binding protein epsilon level in Chronic kidney disease with hypertension and no diabetes (21208_163) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CCAAT/enhancer-binding protein epsilon in blood serum http://purl.obolibrary.org/obo/OBA_2040983 GCST90235625 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA polymerase beta level in Chronic kidney disease with hypertension and no diabetes (21210_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA polymerase beta in blood serum http://purl.obolibrary.org/obo/OBA_2042959 GCST90235626 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prohibitin-2 level in Chronic kidney disease with hypertension and no diabetes (21217_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prohibitin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042871 GCST90235627 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RPA-interacting protein level in Chronic kidney disease with hypertension and no diabetes (21219_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RPA-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043315 GCST90235628 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein SAR1b level in Chronic kidney disease with hypertension and no diabetes (21220_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of GTP-binding protein SAR1b in blood serum http://purl.obolibrary.org/obo/OBA_2043381 GCST90235629 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin B9 level in Chronic kidney disease with hypertension and no diabetes (21221_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin B9 in blood serum http://purl.obolibrary.org/obo/OBA_2043464 GCST90235630 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SULT 1A1*2 level in Chronic kidney disease with hypertension and no diabetes (21227_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 1A1 in blood serum http://purl.obolibrary.org/obo/OBA_2043725 GCST90235631 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane and immunoglobulin domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (21229_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane and immunoglobulin domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044593 GCST90235632 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal acetylcholine receptor subunit alpha-5 level in Chronic kidney disease with hypertension and no diabetes (21231_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuronal acetylcholine receptor subunit alpha-5 in blood serum http://purl.obolibrary.org/obo/OBA_2041017 GCST90235633 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Benign Prostate specific Antigen level in Chronic kidney disease with hypertension and no diabetes (21232_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostate-specific antigen in blood serum http://purl.obolibrary.org/obo/OBA_2040412 GCST90235634 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat and SOCS box protein 13 level in Chronic kidney disease with hypertension and no diabetes (21234_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ankyrin repeat and SOCS box protein 13 in blood serum http://purl.obolibrary.org/obo/OBA_2040691 GCST90235635 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Importin subunit alpha-6 level in Chronic kidney disease with hypertension and no diabetes (21235_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of importin subunit alpha-6 in blood serum http://purl.obolibrary.org/obo/OBA_2042134 GCST90235636 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted frizzled-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (14042_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 secreted frizzled-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020718 GCST90234148 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Early endosome antigen 1 level in Chronic kidney disease with hypertension and no diabetes (14043_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of early endosome antigen 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041416 GCST90234149 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor coactivator 2 level in Chronic kidney disease with hypertension and no diabetes (14045_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor coactivator 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042530 GCST90234150 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brain-derived neurotrophic factor level in Chronic kidney disease with hypertension and no diabetes (14047_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 brain-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0011018 GCST90234151 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 Receptor accessory protein level in Chronic kidney disease with hypertension and no diabetes (14048_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-1 receptor accessory protein in blood serum http://purl.obolibrary.org/obo/OBA_2042008 GCST90234152 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-7 level in Chronic kidney disease with hypertension and no diabetes (14049_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-7 in blood serum http://purl.obolibrary.org/obo/OBA_2040264 GCST90234153 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A4 level in Chronic kidney disease with hypertension and no diabetes (14050_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A4 measurement http://www.ebi.ac.uk/efo/EFO_0020356 GCST90234154 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein C2 level in Chronic kidney disease with hypertension and no diabetes (14051_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein C2 in blood serum http://purl.obolibrary.org/obo/OBA_2041606 GCST90234155 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein unc-13 homolog A level in Chronic kidney disease with hypertension and no diabetes (14052_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein unc-13 homolog A in blood serum http://purl.obolibrary.org/obo/OBA_2044034 GCST90234156 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-15 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (14054_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-15 receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042001 GCST90234157 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycoprotein hormones alpha chain level in Chronic kidney disease with hypertension and no diabetes (14056_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycoprotein hormones alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040994 GCST90234158 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 15 level in Chronic kidney disease with hypertension and no diabetes (14057_68) 466 African American individuals NA Illumina [14870897] (imputed) 1 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90234159 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 11 level in Chronic kidney disease with hypertension and no diabetes (14061_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90234160 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oncostatin-M level in Chronic kidney disease with hypertension and no diabetes (14063_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 oncostatin-M measurement http://www.ebi.ac.uk/efo/EFO_0010792 GCST90234161 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidoglycan recognition protein 1 level in Chronic kidney disease with hypertension and no diabetes (14064_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90234162 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD5 level in Chronic kidney disease with hypertension and no diabetes (14065_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234163 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (14066_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042271 GCST90234164 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plakophilin-2 level in Chronic kidney disease with hypertension and no diabetes (14067_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plakophilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042909 GCST90234165 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 25 level in Chronic kidney disease with hypertension and no diabetes (14068_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 25 measurement http://www.ebi.ac.uk/efo/EFO_0008050 GCST90234166 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 4 level in Chronic kidney disease with hypertension and no diabetes (14069_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase 4 measurement http://www.ebi.ac.uk/efo/EFO_0020230 GCST90234167 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intersectin-1 level in Chronic kidney disease with hypertension and no diabetes (14070_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of intersectin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042065 GCST90234168 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemopexin level in Chronic kidney disease with hypertension and no diabetes (14073_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90234169 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SHC-transforming protein 2 level in Chronic kidney disease with hypertension and no diabetes (14074_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SHC-transforming protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040423 GCST90234170 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-S level in Chronic kidney disease with hypertension and no diabetes (14076_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin-S measurement http://www.ebi.ac.uk/efo/EFO_0020300 GCST90234171 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ficolin-3 level in Chronic kidney disease with hypertension and no diabetes (14077_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 ficolin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020392 GCST90234172 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase kinase kinase 11 level in Chronic kidney disease with hypertension and no diabetes (21406_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase kinase kinase 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042287 GCST90235712 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thimet oligopeptidase level in Chronic kidney disease with hypertension and no diabetes (21429_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thimet oligopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2043843 GCST90235713 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic phospholipase A2 alpha level in Chronic kidney disease with hypertension and no diabetes (21430_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosolic phospholipase A2 in blood serum http://purl.obolibrary.org/obo/OBA_2042915 GCST90235714 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Group 10 secretory phospholipase A2 level in Chronic kidney disease with hypertension and no diabetes (2949_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 group 10 secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020423 GCST90237159 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (2950_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020476 GCST90237160 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor I level in Chronic kidney disease with hypertension and no diabetes (2952_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0004628 GCST90237161 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Luteinizing hormone level in Chronic kidney disease with hypertension and no diabetes (2953_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 luteinizing hormone measurement http://www.ebi.ac.uk/efo/EFO_0007002 GCST90237162 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil collagenase level in Chronic kidney disease with hypertension and no diabetes (2954_56) 466 African American individuals NA Illumina [14870897] (imputed) 1 neutrophil collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008248 GCST90237163 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Properdin level in Chronic kidney disease with hypertension and no diabetes (2960_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 properdin measurement http://www.ebi.ac.uk/efo/EFO_0008269 GCST90237164 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitamin K-dependent protein C level in Chronic kidney disease with hypertension and no diabetes (2961_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 vitamin K-dependent protein C measurement http://www.ebi.ac.uk/efo/EFO_0008318 GCST90237165 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Parathyroid hormone-related protein level in Chronic kidney disease with hypertension and no diabetes (2962_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 parathyroid hormone-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020622 GCST90237166 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stem cell growth factor-beta level in Chronic kidney disease with hypertension and no diabetes (2966_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 stem Cell Growth Factor beta measurement http://www.ebi.ac.uk/efo/EFO_0008292 GCST90237167 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular cell adhesion protein 1 level in Chronic kidney disease with hypertension and no diabetes (2967_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 vascular cell adhesion protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020846 GCST90237168 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 15 level in Chronic kidney disease with hypertension and no diabetes (2968_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 15 measurement http://www.ebi.ac.uk/efo/EFO_0020794 GCST90237169 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase receptor R3 level in Chronic kidney disease with hypertension and no diabetes (2969_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 serine/threonine-protein kinase receptor R3 measurement http://www.ebi.ac.uk/efo/EFO_0020733 GCST90237170 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amphiregulin level in Chronic kidney disease with hypertension and no diabetes (2970_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 amphiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020144 GCST90237171 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 7 level in Chronic kidney disease with hypertension and no diabetes (2972_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 bone morphogenetic protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020187 GCST90237172 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet glycoprotein 4 level in Chronic kidney disease with hypertension and no diabetes (2973_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 platelet glycoprotein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008262 GCST90237173 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-1 level in Chronic kidney disease with hypertension and no diabetes (2974_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 contactin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020286 GCST90237174 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Connective tissue growth factor level in Chronic kidney disease with hypertension and no diabetes (2975_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 connective tissue growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020284 GCST90237175 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmoglein-1 level in Chronic kidney disease with hypertension and no diabetes (2976_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 desmoglein-1 measurement http://www.ebi.ac.uk/efo/EFO_0020321 GCST90237176 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 5 level in Chronic kidney disease with hypertension and no diabetes (2979_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-X-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008058 GCST90237177 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelial cell-selective adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (2981_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90237178 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-4 level in Chronic kidney disease with hypertension and no diabetes (2982_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020398 GCST90237179 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth-regulated alpha protein level in Chronic kidney disease with hypertension and no diabetes (2985_35) 466 African American individuals NA Illumina [14870897] (imputed) 3 growth-regulated alpha protein measurement http://www.ebi.ac.uk/efo/EFO_0008146 GCST90237180 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gro-gamma level in Chronic kidney disease with hypertension and no diabetes (2986_49) 466 African American individuals NA Illumina [14870897] (imputed) 6 level of C-X-C motif chemokine 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041208 GCST90237181 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H1.2 level in Chronic kidney disease with hypertension and no diabetes (2987_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone H1.2 measurement http://www.ebi.ac.uk/efo/EFO_0021966 GCST90237182 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon gamma level in Chronic kidney disease with hypertension and no diabetes (2989_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90237183 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor type 1 level in Chronic kidney disease with hypertension and no diabetes (2991_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-1 receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020487 GCST90237184 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17 receptor A level in Chronic kidney disease with hypertension and no diabetes (2992_59) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-17 receptor A in blood serum http://purl.obolibrary.org/obo/OBA_2040283 GCST90237185 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-18 receptor accessory protein level in Chronic kidney disease with hypertension and no diabetes (2993_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-18 receptor accessory protein in blood serum http://purl.obolibrary.org/obo/OBA_2040285 GCST90237186 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor-like 2 level in Chronic kidney disease with hypertension and no diabetes (2994_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-1 receptor-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042011 GCST90237187 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctional adhesion molecule B level in Chronic kidney disease with hypertension and no diabetes (2997_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 junctional adhesion molecule B measurement http://www.ebi.ac.uk/efo/EFO_0020509 GCST90237188 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctional adhesion molecule C level in Chronic kidney disease with hypertension and no diabetes (2998_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 junctional adhesion molecule C measurement http://www.ebi.ac.uk/efo/EFO_0020510 GCST90237189 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Limbic system-associated membrane protein level in Chronic kidney disease with hypertension and no diabetes (2999_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 limbic system-associated membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0020537 GCST90237190 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mannose-binding protein C level in Chronic kidney disease with hypertension and no diabetes (3000_66) 466 African American individuals NA Illumina [14870897] (imputed) 1 mannose-binding protein C measurement http://www.ebi.ac.uk/efo/EFO_0008224 GCST90237191 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Natural cytotoxicity triggering receptor 3 level in Chronic kidney disease with hypertension and no diabetes (3003_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 natural cytotoxicity triggering receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008243 GCST90237192 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death 1 ligand 2 level in Chronic kidney disease with hypertension and no diabetes (3004_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 programmed cell death 1 ligand 2 measurement http://www.ebi.ac.uk/efo/EFO_0008268 GCST90237193 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 1 level in Chronic kidney disease with hypertension and no diabetes (3005_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein phosphatase non-receptor type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020834 GCST90237194 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 9 level in Chronic kidney disease with hypertension and no diabetes (3007_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 sialic acid-binding Ig-like lectin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008286 GCST90237195 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming growth factor beta receptor type 3 level in Chronic kidney disease with hypertension and no diabetes (3009_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 transforming growth factor beta receptor type 3 measurement http://www.ebi.ac.uk/efo/EFO_0020779 GCST90237196 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thymic stromal lymphopoietin level in Chronic kidney disease with hypertension and no diabetes (3010_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 thymic stromal lymphopoietin measurement http://www.ebi.ac.uk/efo/EFO_0020772 GCST90237197 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytotoxic T-lymphocyte protein 4 level in Chronic kidney disease with hypertension and no diabetes (3022_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytotoxic t-lymphocyte protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020312 GCST90237198 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-2-antiplasmin level in Chronic kidney disease with hypertension and no diabetes (3024_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-2-antiplasmin measurement http://www.ebi.ac.uk/efo/EFO_0020137 GCST90237199 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 2 level in Chronic kidney disease with hypertension and no diabetes (3025_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008129 GCST90237200 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpastatin level in Chronic kidney disease with hypertension and no diabetes (3026_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 calpastatin measurement http://www.ebi.ac.uk/efo/EFO_0008065 GCST90237201 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ck-beta-8-1 level in Chronic kidney disease with hypertension and no diabetes (3028_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 Ck-beta-8-1 measurement http://www.ebi.ac.uk/efo/EFO_0008085 GCST90237202 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD209 antigen level in Chronic kidney disease with hypertension and no diabetes (3029_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90237203 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follicle stimulating hormone level in Chronic kidney disease with hypertension and no diabetes (3032_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 follicle stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004768 GCST90237204 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-2 level in Chronic kidney disease with hypertension and no diabetes (3033_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020397 GCST90237205 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glial fibrillary acidic protein level in Chronic kidney disease with hypertension and no diabetes (3034_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 glial fibrillary acidic protein measurement http://www.ebi.ac.uk/efo/EFO_0020404 GCST90237206 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-19 level in Chronic kidney disease with hypertension and no diabetes (3035_80) 466 African American individuals NA Illumina [14870897] (imputed) 1 interleukin 19 measurement http://www.ebi.ac.uk/efo/EFO_0008180 GCST90237207 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 beta level in Chronic kidney disease with hypertension and no diabetes (3037_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-1 beta measurement http://www.ebi.ac.uk/efo/EFO_0004812 GCST90237208 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 11 level in Chronic kidney disease with hypertension and no diabetes (3038_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90237209 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type mannose receptor 2 level in Chronic kidney disease with hypertension and no diabetes (3041_55) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-type mannose receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020204 GCST90237210 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myoglobin level in Chronic kidney disease with hypertension and no diabetes (3042_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 myoglobin measurement http://www.ebi.ac.uk/efo/EFO_0005057 GCST90237211 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPARC level in Chronic kidney disease with hypertension and no diabetes (3043_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90237212 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 18 level in Chronic kidney disease with hypertension and no diabetes (3044_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 18 measurement http://www.ebi.ac.uk/efo/EFO_0008046 GCST90237213 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Resistin level in Chronic kidney disease with hypertension and no diabetes (3046_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 resistin measurement http://www.ebi.ac.uk/efo/EFO_0004819 GCST90237214 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trypsin-1 level in Chronic kidney disease with hypertension and no diabetes (3049_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 trypsin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020790 GCST90237215 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 6, soluble form level in Chronic kidney disease with hypertension and no diabetes (3052_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 6, soluble form measurement http://www.ebi.ac.uk/efo/EFO_0020797 GCST90237216 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fms-related tyrosine kinase 3 ligand level in Chronic kidney disease with hypertension and no diabetes (3053_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90237217 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Haptoglobin level in Chronic kidney disease with hypertension and no diabetes (3054_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 haptoglobin measurement http://www.ebi.ac.uk/efo/EFO_0004640 GCST90237218 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-4 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3055_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-4 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020507 GCST90237219 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2-D type II integral membrane protein level in Chronic kidney disease with hypertension and no diabetes (3056_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 NKG2-D type II integral membrane protein measurement http://www.ebi.ac.uk/efo/EFO_0008250 GCST90237220 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 13B level in Chronic kidney disease with hypertension and no diabetes (3059_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 13B measurement http://www.ebi.ac.uk/efo/EFO_0020793 GCST90237221 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C9 level in Chronic kidney disease with hypertension and no diabetes (3060_43) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90237222 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin B level in Chronic kidney disease with hypertension and no diabetes (3061_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90237223 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 5 level in Chronic kidney disease with hypertension and no diabetes (3065_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 5 measurement http://www.ebi.ac.uk/efo/EFO_0010784 GCST90237224 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-3 level in Chronic kidney disease with hypertension and no diabetes (3066_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-3 measurement http://www.ebi.ac.uk/efo/EFO_0008137 GCST90237225 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 9 level in Chronic kidney disease with hypertension and no diabetes (3067_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 growth/differentiation factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020430 GCST90237226 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin M level in Chronic kidney disease with hypertension and no diabetes (3069_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 serum IgM measurement http://www.ebi.ac.uk/efo/EFO_0004993 GCST90237227 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-2 level in Chronic kidney disease with hypertension and no diabetes (3070_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040286 GCST90237228 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-13 level in Chronic kidney disease with hypertension and no diabetes (3072_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-13 in blood serum http://purl.obolibrary.org/obo/OBA_2040280 GCST90237229 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-18-binding protein level in Chronic kidney disease with hypertension and no diabetes (3073_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 interleukin-18-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020495 GCST90237230 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chordin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (3362_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 chordin-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020257 GCST90237342 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase CSK level in Chronic kidney disease with hypertension and no diabetes (3363_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase CSK measurement http://www.ebi.ac.uk/efo/EFO_0020820 GCST90237343 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin L2 level in Chronic kidney disease with hypertension and no diabetes (3364_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin L2 measurement http://www.ebi.ac.uk/efo/EFO_0020244 GCST90237344 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fetuin-B level in Chronic kidney disease with hypertension and no diabetes (3367_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 fetuin-B measurement http://www.ebi.ac.uk/efo/EFO_0008128 GCST90237345 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granzyme H level in Chronic kidney disease with hypertension and no diabetes (3373_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 granzyme h measurement http://www.ebi.ac.uk/efo/EFO_0020419 GCST90237346 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase HCK level in Chronic kidney disease with hypertension and no diabetes (3374_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase HCK measurement http://www.ebi.ac.uk/efo/EFO_0020824 GCST90237347 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17 receptor D level in Chronic kidney disease with hypertension and no diabetes (3376_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-17 receptor D in blood serum http://purl.obolibrary.org/obo/OBA_2042003 GCST90237348 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-7 level in Chronic kidney disease with hypertension and no diabetes (3378_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-7 measurement http://www.ebi.ac.uk/efo/EFO_0008195 GCST90237349 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C iota type level in Chronic kidney disease with hypertension and no diabetes (3379_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein kinase c iota type measurement http://www.ebi.ac.uk/efo/EFO_0020681 GCST90237350 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase Lyn, isoform B level in Chronic kidney disease with hypertension and no diabetes (3381_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase LYN, isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020828 GCST90237351 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase PAK 3 level in Chronic kidney disease with hypertension and no diabetes (3387_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase PAK 3 measurement http://www.ebi.ac.uk/efo/EFO_0020728 GCST90237352 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DS2 level in Chronic kidney disease with hypertension and no diabetes (10428_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of killer cell immunoglobulin-like receptor 2DS2 in blood serum http://purl.obolibrary.org/obo/OBA_2042107 GCST90232865 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 4F2 cell-surface antigen heavy chain level in Chronic kidney disease with hypertension and no diabetes (10430_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232866 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein KIAA1644 level in Chronic kidney disease with hypertension and no diabetes (10432_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 high content analysis of cells by molecular content http://www.ebi.ac.uk/efo/EFO_0005398 GCST90232867 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase level in Chronic kidney disease with hypertension and no diabetes (10435_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase in blood serum http://purl.obolibrary.org/obo/OBA_2040532 GCST90232868 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulocyte-macrophage colony-stimulating factor receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (10438_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of granulocyte-macrophage colony-stimulating factor receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040276 GCST90232869 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-amylase 2B level in Chronic kidney disease with hypertension and no diabetes (10439_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-amylase 2B in blood serum http://purl.obolibrary.org/obo/OBA_2040586 GCST90232870 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CXADR-like membrane protein level in Chronic kidney disease with hypertension and no diabetes (10440_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232871 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 190 level in Chronic kidney disease with hypertension and no diabetes (10442_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transmembrane protein 190 in blood serum http://purl.obolibrary.org/obo/OBA_2044430 GCST90232872 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein M level in Chronic kidney disease with hypertension and no diabetes (10445_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 apolipoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0021945 GCST90232873 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyadenylate-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (10447_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyadenylate-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042734 GCST90232874 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein shisa-2 homolog level in Chronic kidney disease with hypertension and no diabetes (10449_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein shisa-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043501 GCST90232875 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleobindin-1 level in Chronic kidney disease with hypertension and no diabetes (10451_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleobindin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042660 GCST90232876 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 20 level in Chronic kidney disease with hypertension and no diabetes (10453_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 20 in blood serum http://purl.obolibrary.org/obo/OBA_2040978 GCST90232877 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 16 level in Chronic kidney disease with hypertension and no diabetes (10454_99) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 16 in blood serum http://purl.obolibrary.org/obo/OBA_2044642 GCST90232878 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like protein Nedd8 level in Chronic kidney disease with hypertension and no diabetes (21445_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD8 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042551 GCST90235722 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-10 level in Chronic kidney disease with hypertension and no diabetes (21450_333) 466 African American individuals NA Illumina [14870897] (imputed) 0 caspase-10 measurement http://www.ebi.ac.uk/efo/EFO_0020239 GCST90235723 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynamin-1-like protein level in Chronic kidney disease with hypertension and no diabetes (21452_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of dynamin-1-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2041335 GCST90235724 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coenzyme Q-binding protein COQ10 homolog A, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21457_141) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coenzyme Q-binding protein COQ10 homolog A, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041100 GCST90235725 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (21475_137) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thioredoxin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043971 GCST90235726 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endonuclease 8-like 2 level in Chronic kidney disease with hypertension and no diabetes (21476_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endonuclease 8-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042555 GCST90235727 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage erythroblast attacher level in Chronic kidney disease with hypertension and no diabetes (21477_105) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein transferase MAEA in blood serum http://purl.obolibrary.org/obo/OBA_2042261 GCST90235728 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SMAD5 level in Chronic kidney disease with hypertension and no diabetes (21478_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of smad5 in blood serum http://purl.obolibrary.org/obo/OBA_2040217 GCST90235729 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD82 antigen level in Chronic kidney disease with hypertension and no diabetes (21480_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD82 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040947 GCST90235730 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-dependent protein kinase type I-alpha regulatory subunit level in Chronic kidney disease with hypertension and no diabetes (21483_155) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-dependent protein kinase type I-alpha regulatory subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043026 GCST90235731 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biogenesis of lysosome-related organelles complex 1 subunit 6 level in Chronic kidney disease with hypertension and no diabetes (21487_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of biogenesis of lysosome-related organelles complex 1 subunit 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042924 GCST90235732 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular adhesion protein-1 level in Chronic kidney disease with hypertension and no diabetes (21491_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of membrane primary amine oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2040606 GCST90235733 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Clusterin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (21492_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of clusterin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041061 GCST90235734 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prosaposin receptor GPR37 level in Chronic kidney disease with hypertension and no diabetes (21495_134) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prosaposin receptor GPR37 in blood serum http://purl.obolibrary.org/obo/OBA_2040248 GCST90235735 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hypoxia up-regulated protein 1 level in Chronic kidney disease with hypertension and no diabetes (21497_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hypoxia up-regulated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041963 GCST90235736 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-aminoadipic semialdehyde dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (21498_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of alpha-aminoadipic semialdehyde dehydrogenase in blood serum http://purl.obolibrary.org/obo/OBA_2040566 GCST90235737 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5-demethoxyubiquinone hydroxylase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21499_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquinone biosynthesis protein COQ7 in blood serum http://purl.obolibrary.org/obo/OBA_2041103 GCST90235738 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Farnesyl pyrophosphate synthetase level in Chronic kidney disease with hypertension and no diabetes (21501_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of farnesyl pyrophosphate synthase in blood serum http://purl.obolibrary.org/obo/OBA_2041569 GCST90235739 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyrotropin receptor level in Chronic kidney disease with hypertension and no diabetes (21503_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thyrotropin receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040318 GCST90235740 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 2C 2 level in Chronic kidney disease with hypertension and no diabetes (21504_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein argonaute-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041442 GCST90235741 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COMM domain-containing protein 8 level in Chronic kidney disease with hypertension and no diabetes (21507_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of COMM domain-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044734 GCST90235742 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylneuraminide alpha-2,8-sialyltransferase level in Chronic kidney disease with hypertension and no diabetes (21508_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of alpha-N-acetylneuraminide alpha-2,8-sialyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043681 GCST90235743 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycosyltransferase 8 domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (21509_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycosyltransferase 8 domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044616 GCST90235744 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G protein-coupled receptor kinase 5 level in Chronic kidney disease with hypertension and no diabetes (21510_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of G protein-coupled receptor kinase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041793 GCST90235745 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ER degradation-enhancing alpha-mannosidase-like 2 level in Chronic kidney disease with hypertension and no diabetes (21512_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ER degradation-enhancing alpha-mannosidase-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041410 GCST90235746 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine kinase 10 level in Chronic kidney disease with hypertension and no diabetes (21569_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine/threonine-protein kinase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043699 GCST90235772 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Xylosyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (21572_91) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of xylosyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044156 GCST90235773 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FK506-binding protein 5 level in Chronic kidney disease with hypertension and no diabetes (21577_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase FKBP5 in blood serum http://purl.obolibrary.org/obo/OBA_2041590 GCST90235774 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin-binding protein C, cardiac-type level in Chronic kidney disease with hypertension and no diabetes (21579_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin-binding protein C, cardiac-type in blood serum http://purl.obolibrary.org/obo/OBA_2042475 GCST90235775 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 15; EC=2.7.11.22 level in Chronic kidney disease with hypertension and no diabetes (21581_87) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cyclin-dependent kinase 15 in blood serum http://purl.obolibrary.org/obo/OBA_2042858 GCST90235776 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S ribosomal protein L26-like 1 level in Chronic kidney disease with hypertension and no diabetes (21583_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S ribosomal protein L26-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043320 GCST90235777 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD4 level in Chronic kidney disease with hypertension and no diabetes (21588_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD4 in blood serum http://purl.obolibrary.org/obo/OBA_2044627 GCST90235778 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Developmental pluripotency-associated protein 4 level in Chronic kidney disease with hypertension and no diabetes (21589_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of developmental pluripotency-associated protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041354 GCST90235779 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat family A protein 2 level in Chronic kidney disease with hypertension and no diabetes (21590_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat family A protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040590 GCST90235780 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic beta-glucosidase level in Chronic kidney disease with hypertension and no diabetes (21592_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosolic beta-glucosidase in blood serum http://purl.obolibrary.org/obo/OBA_2041679 GCST90235781 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 43 level in Chronic kidney disease with hypertension and no diabetes (21595_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 43 in blood serum http://purl.obolibrary.org/obo/OBA_2044262 GCST90235782 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystathionine gamma-lyase level in Chronic kidney disease with hypertension and no diabetes (21599_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cystathionine gamma-lyase in blood serum http://purl.obolibrary.org/obo/OBA_2041184 GCST90235783 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-catenin-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (21600_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-catenin-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041189 GCST90235784 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein CutA level in Chronic kidney disease with hypertension and no diabetes (21604_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein CutA in blood serum http://purl.obolibrary.org/obo/OBA_2041201 GCST90235785 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gem-associated protein 6 level in Chronic kidney disease with hypertension and no diabetes (21614_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gem-associated protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041702 GCST90235786 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NF-kappa-B inhibitor-interacting Ras-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (21624_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NF-kappa-B inhibitor-interacting Ras-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042587 GCST90235787 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation elongation factor 1 epsilon-1 level in Chronic kidney disease with hypertension and no diabetes (21628_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation elongation factor 1 epsilon-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041420 GCST90235788 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear cap-binding protein subunit 2 level in Chronic kidney disease with hypertension and no diabetes (21636_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear cap-binding protein subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042524 GCST90235789 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase-like 3 level in Chronic kidney disease with hypertension and no diabetes (21638_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase-like 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042990 GCST90235790 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S20 level in Chronic kidney disease with hypertension and no diabetes (21643_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 40S ribosomal protein S20 in blood serum http://purl.obolibrary.org/obo/OBA_2043333 GCST90235791 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Smad nuclear-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (21645_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of smad nuclear-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043569 GCST90235792 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermidine synthase level in Chronic kidney disease with hypertension and no diabetes (21647_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spermidine synthase in blood serum http://purl.obolibrary.org/obo/OBA_2043656 GCST90235793 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-17 level in Chronic kidney disease with hypertension and no diabetes (21649_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of syntaxin-17 in blood serum http://purl.obolibrary.org/obo/OBA_2043710 GCST90235794 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin-like protein 4A level in Chronic kidney disease with hypertension and no diabetes (21651_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of thioredoxin-like protein 4A in blood serum http://purl.obolibrary.org/obo/OBA_2043972 GCST90235795 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LisH domain-containing protein FOPNL level in Chronic kidney disease with hypertension and no diabetes (21655_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of centrosomal protein 20 in blood serum http://purl.obolibrary.org/obo/OBA_2044529 GCST90235796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-7 level in Chronic kidney disease with hypertension and no diabetes (21513_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caspase-7 in blood serum http://purl.obolibrary.org/obo/OBA_2040409 GCST90235747 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet glycoprotein Ib beta chain level in Chronic kidney disease with hypertension and no diabetes (21514_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of platelet glycoprotein Ib beta chain in blood serum http://purl.obolibrary.org/obo/OBA_2040353 GCST90235748 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acetoacetyl-CoA synthetase level in Chronic kidney disease with hypertension and no diabetes (21515_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acetoacetyl-CoA synthetase in blood serum http://purl.obolibrary.org/obo/OBA_2040453 GCST90235749 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptophan 5-hydroxylase 1 level in Chronic kidney disease with hypertension and no diabetes (21521_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tryptophan 5-hydroxylase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043909 GCST90235750 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin-linked kinase-associated serine/threonine phosphatase 2C level in Chronic kidney disease with hypertension and no diabetes (21523_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin-linked kinase-associated serine/threonine phosphatase 2C in blood serum http://purl.obolibrary.org/obo/OBA_2042019 GCST90235751 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 5 level in Chronic kidney disease with hypertension and no diabetes (21524_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044067 GCST90235752 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bcl-2-modifying factor level in Chronic kidney disease with hypertension and no diabetes (21528_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Bcl-2-modifying factor in blood serum http://purl.obolibrary.org/obo/OBA_2040810 GCST90235753 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-associated and SH3 domain-containing protein A level in Chronic kidney disease with hypertension and no diabetes (21529_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-associated and SH3 domain-containing protein A in blood serum http://purl.obolibrary.org/obo/OBA_2043986 GCST90235754 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte-specific protein 1 level in Chronic kidney disease with hypertension and no diabetes (21533_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lymphocyte-specific protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042244 GCST90235755 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alanyl-tRNA editing protein Aarsd1 level in Chronic kidney disease with hypertension and no diabetes (21535_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alanyl-tRNA editing protein Aarsd1 in blood serum http://purl.obolibrary.org/obo/OBA_2044247 GCST90235756 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complexin-3 level in Chronic kidney disease with hypertension and no diabetes (21536_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complexin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041119 GCST90235757 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Selenocysteine lyase level in Chronic kidney disease with hypertension and no diabetes (21537_33) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of selenocysteine lyase in blood serum http://purl.obolibrary.org/obo/OBA_2043402 GCST90235758 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-6 level in Chronic kidney disease with hypertension and no diabetes (21539_139) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-6 in blood serum http://purl.obolibrary.org/obo/OBA_2043756 GCST90235759 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bridging integrator 2 level in Chronic kidney disease with hypertension and no diabetes (21540_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bridging integrator 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040799 GCST90235760 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Atlastin-3 level in Chronic kidney disease with hypertension and no diabetes (21544_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of atlastin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040723 GCST90235761 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Musculoskeletal embryonic nuclear protein 1 level in Chronic kidney disease with hypertension and no diabetes (21545_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of musculoskeletal embryonic nuclear protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042464 GCST90235762 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G-protein coupled receptor D1 level in Chronic kidney disease with hypertension and no diabetes (21546_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of adhesion G-protein coupled receptor D1 in blood serum http://purl.obolibrary.org/obo/OBA_2044505 GCST90235763 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dentin matrix protein 4 level in Chronic kidney disease with hypertension and no diabetes (21547_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of extracellular serine/threonine protein kinase Fam20C in blood serum http://purl.obolibrary.org/obo/OBA_2044623 GCST90235764 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-glutamyltransferase 5 level in Chronic kidney disease with hypertension and no diabetes (21548_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutathione hydrolase 5 proenzyme in blood serum http://purl.obolibrary.org/obo/OBA_2041713 GCST90235765 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-tectorin level in Chronic kidney disease with hypertension and no diabetes (21549_144) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-tectorin in blood serum http://purl.obolibrary.org/obo/OBA_2043824 GCST90235766 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal acyl-coenzyme A oxidase 1 level in Chronic kidney disease with hypertension and no diabetes (21552_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisomal acyl-coenzyme A oxidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040482 GCST90235767 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM3A level in Chronic kidney disease with hypertension and no diabetes (21555_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM3A in blood serum http://purl.obolibrary.org/obo/OBA_2044488 GCST90235768 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretoglobin family 1D member 1 level in Chronic kidney disease with hypertension and no diabetes (21562_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretoglobin family 1D member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043397 GCST90235769 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. sPLA(2)-XII level in Chronic kidney disease with hypertension and no diabetes (21563_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of group XIIA secretory phospholipase A2 in blood serum http://purl.obolibrary.org/obo/OBA_2042911 GCST90235770 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q tumor necrosis factor-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (21567_214) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q tumor necrosis factor-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040851 GCST90235771 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prohibitin-2 level in Chronic kidney disease with hypertension and no diabetes (21658_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prohibitin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042871 GCST90235797 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein SAR1b level in Chronic kidney disease with hypertension and no diabetes (21660_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of GTP-binding protein SAR1b in blood serum http://purl.obolibrary.org/obo/OBA_2043381 GCST90235798 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dentin matrix protein 4 level in Chronic kidney disease with hypertension and no diabetes (21661_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of extracellular serine/threonine protein kinase Fam20C in blood serum http://purl.obolibrary.org/obo/OBA_2044623 GCST90235799 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity tyrosine-phosphorylation-regulated kinase 3 level in Chronic kidney disease with hypertension and no diabetes (21662_121) 466 African American individuals NA Illumina [14870897] (imputed) 0 dual specificity tyrosine-phosphorylation-regulated kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020337 GCST90235800 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylneuraminide alpha-2,8-sialyltransferase level in Chronic kidney disease with hypertension and no diabetes (21663_149) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetylneuraminide alpha-2,8-sialyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043681 GCST90235801 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Core histone macro-H2A.1 level in Chronic kidney disease with hypertension and no diabetes (21664_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of core histone macro-H2A.1 in blood serum http://purl.obolibrary.org/obo/OBA_2041828 GCST90235802 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B level in Chronic kidney disease with hypertension and no diabetes (21667_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1B in blood serum http://purl.obolibrary.org/obo/OBA_2042819 GCST90235803 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD4-like E3 ubiquitin-protein ligase WWP2 level in Chronic kidney disease with hypertension and no diabetes (21670_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD4-like E3 ubiquitin-protein ligase WWP2 in blood serum http://purl.obolibrary.org/obo/OBA_2044146 GCST90235804 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin subfamily 1 member A1 level in Chronic kidney disease with hypertension and no diabetes (21674_132) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of butyrophilin subfamily 1 member A1 in blood serum http://purl.obolibrary.org/obo/OBA_2040835 GCST90235805 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PAI-2 level in Chronic kidney disease with hypertension and no diabetes (21676_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of plasminogen activator inhibitor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044386 GCST90235806 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-20 level in Chronic kidney disease with hypertension and no diabetes (21679_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-20 in blood serum http://purl.obolibrary.org/obo/OBA_2040960 GCST90235807 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADAM 28 level in Chronic kidney disease with hypertension and no diabetes (21681_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 28 in blood serum http://purl.obolibrary.org/obo/OBA_2040499 GCST90235808 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DCC level in Chronic kidney disease with hypertension and no diabetes (21685_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of netrin receptor DCC in blood serum http://purl.obolibrary.org/obo/OBA_2041237 GCST90235809 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1 regulatory subunit 29 level in Chronic kidney disease with hypertension and no diabetes (21687_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1 regulatory subunit 29 in blood serum http://purl.obolibrary.org/obo/OBA_2044531 GCST90235810 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin S level in Chronic kidney disease with hypertension and no diabetes (3181_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin S measurement http://www.ebi.ac.uk/efo/EFO_0008073 GCST90237256 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleoside triphosphate diphosphohydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (3182_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90237257 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation factor VII level in Chronic kidney disease with hypertension and no diabetes (3184_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of coagulation factor VII in blood serum http://purl.obolibrary.org/obo/OBA_2041535 GCST90237258 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C2 level in Chronic kidney disease with hypertension and no diabetes (3186_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C2 measurement http://www.ebi.ac.uk/efo/EFO_0020274 GCST90237259 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich secretory protein 3 level in Chronic kidney disease with hypertension and no diabetes (3187_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 cysteine-rich secretory protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020301 GCST90237260 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Enteropeptidase level in Chronic kidney disease with hypertension and no diabetes (3189_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 enteropeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020349 GCST90237261 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP, kazal, immunoglobulin, kunitz and NTR domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (3191_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 wap, kazal, immunoglobulin, kunitz and ntr domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020852 GCST90237262 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic non-specific dipeptidase level in Chronic kidney disease with hypertension and no diabetes (3192_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytosolic non-specific dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0020310 GCST90237263 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet glycoprotein VI level in Chronic kidney disease with hypertension and no diabetes (3194_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 platelet glycoprotein VI measurement http://www.ebi.ac.uk/efo/EFO_0008263 GCST90237264 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulysin level in Chronic kidney disease with hypertension and no diabetes (3195_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90237265 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hyaluronan and proteoglycan link protein 1 level in Chronic kidney disease with hypertension and no diabetes (3196_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 hyaluronan and proteoglycan link protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020459 GCST90237266 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-31 level in Chronic kidney disease with hypertension and no diabetes (10455_196) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-31 in blood serum http://purl.obolibrary.org/obo/OBA_2040263 GCST90232879 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-18 receptor accessory protein level in Chronic kidney disease with hypertension and no diabetes (10457_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-18 receptor accessory protein in blood serum http://purl.obolibrary.org/obo/OBA_2040285 GCST90232880 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chitotriosidase-1 level in Chronic kidney disease with hypertension and no diabetes (10460_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90232881 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like peptide INSL5 level in Chronic kidney disease with hypertension and no diabetes (10462_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-like peptide INSL5 in blood serum http://purl.obolibrary.org/obo/OBA_2042036 GCST90232882 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intestinal-type alkaline phosphatase level in Chronic kidney disease with hypertension and no diabetes (10463_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of intestinal alkaline phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2040574 GCST90232883 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anthrax toxin receptor 1 level in Chronic kidney disease with hypertension and no diabetes (10464_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anthrax toxin receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040595 GCST90232884 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 14 level in Chronic kidney disease with hypertension and no diabetes (10472_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0020805 GCST90232885 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trefoil factor 2 level in Chronic kidney disease with hypertension and no diabetes (10473_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 trefoil factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0021846 GCST90232886 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromelysin-2 level in Chronic kidney disease with hypertension and no diabetes (10479_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 stromelysin‐2 measurement http://www.ebi.ac.uk/efo/EFO_0010621 GCST90232887 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD59 glycoprotein level in Chronic kidney disease with hypertension and no diabetes (10480_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD59 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0021924 GCST90232888 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1 level in Chronic kidney disease with hypertension and no diabetes (10490_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232889 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-activated chloride channel regulator 1 level in Chronic kidney disease with hypertension and no diabetes (10496_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-activated chloride channel regulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041040 GCST90232890 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 106A level in Chronic kidney disease with hypertension and no diabetes (10499_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 106A in blood serum http://purl.obolibrary.org/obo/OBA_2044585 GCST90232891 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF43 level in Chronic kidney disease with hypertension and no diabetes (10505_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 e3 ubiquitin-protein ligase RNF43 measurement http://www.ebi.ac.uk/efo/EFO_0021886 GCST90232892 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane-associated progesterone receptor component 2 level in Chronic kidney disease with hypertension and no diabetes (10506_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane-associated progesterone receptor component 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042870 GCST90232893 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acrosomal protein SP-10 level in Chronic kidney disease with hypertension and no diabetes (10507_166) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acrosomal protein SP-10 in blood serum http://purl.obolibrary.org/obo/OBA_2040486 GCST90232894 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLP adapter and CSK-interacting membrane protein level in Chronic kidney disease with hypertension and no diabetes (10510_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLP adapter and CSK-interacting membrane protein in blood serum http://purl.obolibrary.org/obo/OBA_2044658 GCST90232895 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine receptor common subunit beta level in Chronic kidney disease with hypertension and no diabetes (10512_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232896 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calsenilin level in Chronic kidney disease with hypertension and no diabetes (10513_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calsenilin in blood serum http://purl.obolibrary.org/obo/OBA_2042090 GCST90232897 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin-H2 D-isomerase level in Chronic kidney disease with hypertension and no diabetes (10514_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostaglandin-H2 D-isomerase in blood serum http://purl.obolibrary.org/obo/OBA_2043088 GCST90232898 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix-remodeling-associated protein 8 level in Chronic kidney disease with hypertension and no diabetes (10521_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrix metalloproteinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0008466 GCST90232899 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent RNA helicase A level in Chronic kidney disease with hypertension and no diabetes (10527_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent RNA helicase A in blood serum http://purl.obolibrary.org/obo/OBA_2041300 GCST90232900 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dipeptidase 1 level in Chronic kidney disease with hypertension and no diabetes (10528_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dipeptidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041348 GCST90232901 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-6 level in Chronic kidney disease with hypertension and no diabetes (10530_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit beta type-6 in blood serum http://purl.obolibrary.org/obo/OBA_2043071 GCST90232902 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTPase NRas level in Chronic kidney disease with hypertension and no diabetes (10531_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTPase NRas in blood serum http://purl.obolibrary.org/obo/OBA_2042634 GCST90232903 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-degrading enzyme level in Chronic kidney disease with hypertension and no diabetes (3197_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-degrading enzyme measurement http://www.ebi.ac.uk/efo/EFO_0020472 GCST90237267 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-12 level in Chronic kidney disease with hypertension and no diabetes (3199_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 kallikrein-12 measurement http://www.ebi.ac.uk/efo/EFO_0008194 GCST90237268 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-13 level in Chronic kidney disease with hypertension and no diabetes (3200_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-13 measurement http://www.ebi.ac.uk/efo/EFO_0020512 GCST90237269 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-5 level in Chronic kidney disease with hypertension and no diabetes (3201_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-5 measurement http://www.ebi.ac.uk/efo/EFO_0020515 GCST90237270 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kremen protein 2 level in Chronic kidney disease with hypertension and no diabetes (3202_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 kremen protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020523 GCST90237271 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukotriene A-4 hydrolase level in Chronic kidney disease with hypertension and no diabetes (3204_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 leukotriene a-4 hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020535 GCST90237272 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphatic vessel endothelial hyaluronic acid receptor 1 level in Chronic kidney disease with hypertension and no diabetes (3206_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphatic vessel endothelial hyaluronic acid receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020539 GCST90237273 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrilin-3 level in Chronic kidney disease with hypertension and no diabetes (3208_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020556 GCST90237274 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix extracellular phosphoglycoprotein level in Chronic kidney disease with hypertension and no diabetes (3209_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrix extracellular phosphoglycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020557 GCST90237275 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionine aminopeptidase 1 level in Chronic kidney disease with hypertension and no diabetes (3210_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 methionine aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020568 GCST90237276 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutral ceramidase level in Chronic kidney disease with hypertension and no diabetes (3212_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 neutral ceramidase measurement http://www.ebi.ac.uk/efo/EFO_0008247 GCST90237277 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nidogen-1 level in Chronic kidney disease with hypertension and no diabetes (3213_65) 466 African American individuals NA Illumina [14870897] (imputed) 1 nidogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008249 GCST90237278 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropilin-1 level in Chronic kidney disease with hypertension and no diabetes (3214_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuropilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020603 GCST90237279 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polymeric immunoglobulin receptor level in Chronic kidney disease with hypertension and no diabetes (3216_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 polymeric immunoglobulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008267 GCST90237280 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate carboxypeptidase 2 level in Chronic kidney disease with hypertension and no diabetes (3218_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90237281 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proto-oncogene tyrosine-protein kinase receptor Ret level in Chronic kidney disease with hypertension and no diabetes (3220_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 proto-oncogene tyrosine-protein kinase receptor Ret measurement http://www.ebi.ac.uk/efo/EFO_0008272 GCST90237282 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted frizzled-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (3221_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 secreted frizzled-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020718 GCST90237283 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-3A level in Chronic kidney disease with hypertension and no diabetes (3222_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 semaphorin-3A measurement http://www.ebi.ac.uk/efo/EFO_0008278 GCST90237284 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tartrate-resistant acid phosphatase type 5 level in Chronic kidney disease with hypertension and no diabetes (3232_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 tartrate-resistant acid phosphatase type 5 measurement http://www.ebi.ac.uk/efo/EFO_0020763 GCST90237285 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 80 level in Chronic kidney disease with hypertension and no diabetes (3234_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 coiled-coil domain-containing protein 80 measurement http://www.ebi.ac.uk/efo/EFO_0020268 GCST90237286 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (3235_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90237287 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aggrecan core protein level in Chronic kidney disease with hypertension and no diabetes (3280_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 aggrecan core protein measurement http://www.ebi.ac.uk/efo/EFO_0020133 GCST90237288 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming growth factor-beta-induced protein ig-h3 level in Chronic kidney disease with hypertension and no diabetes (3283_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 transforming growth factor-beta-induced protein ig-h3 measurement http://www.ebi.ac.uk/efo/EFO_0008302 GCST90237289 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biglycan level in Chronic kidney disease with hypertension and no diabetes (3284_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 biglycan measurement http://www.ebi.ac.uk/efo/EFO_0020182 GCST90237290 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1r subcomponent level in Chronic kidney disease with hypertension and no diabetes (3285_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C1r subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008090 GCST90237291 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase-related protein 10 level in Chronic kidney disease with hypertension and no diabetes (3289_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase-related protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020233 GCST90237292 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD109 antigen level in Chronic kidney disease with hypertension and no diabetes (3290_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 CD109 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008076 GCST90237293 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low affinity immunoglobulin epsilon Fc receptor level in Chronic kidney disease with hypertension and no diabetes (3291_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 low affinity immunoglobulin epsilon Fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0008210 GCST90237294 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD48 antigen level in Chronic kidney disease with hypertension and no diabetes (3292_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD48 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020247 GCST90237295 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD5 antigen-like level in Chronic kidney disease with hypertension and no diabetes (3293_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD5 antigen-like measurement http://www.ebi.ac.uk/efo/EFO_0020248 GCST90237296 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cryptic protein level in Chronic kidney disease with hypertension and no diabetes (3294_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 cryptic protein measurement http://www.ebi.ac.uk/efo/EFO_0020293 GCST90237297 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-2 level in Chronic kidney disease with hypertension and no diabetes (3296_92) 466 African American individuals NA Illumina [14870897] (imputed) 1 contactin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008100 GCST90237298 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-4 level in Chronic kidney disease with hypertension and no diabetes (3298_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 contactin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020287 GCST90237299 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-5 level in Chronic kidney disease with hypertension and no diabetes (3299_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 contactin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008101 GCST90237300 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-F level in Chronic kidney disease with hypertension and no diabetes (3302_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 cystatin-F measurement http://www.ebi.ac.uk/efo/EFO_0008104 GCST90237301 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-M level in Chronic kidney disease with hypertension and no diabetes (3303_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90237302 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (3305_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 delta-like protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020317 GCST90237303 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low affinity immunoglobulin gamma Fc region receptor II-a level in Chronic kidney disease with hypertension and no diabetes (3309_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 low affinity immunoglobulin gamma Fc region receptor II-a measurement http://www.ebi.ac.uk/efo/EFO_0021969 GCST90237304 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low affinity immunoglobulin gamma Fc region receptor II-b level in Chronic kidney disease with hypertension and no diabetes (3310_62) 466 African American individuals NA Illumina [14870897] (imputed) 1 low affinity immunoglobulin gamma Fc region receptor II-b measurement http://www.ebi.ac.uk/efo/EFO_0021970 GCST90237305 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low affinity immunoglobulin gamma Fc region receptor III-B level in Chronic kidney disease with hypertension and no diabetes (3311_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 low affinity immunoglobulin gamma Fc region receptor III-B measurement http://www.ebi.ac.uk/efo/EFO_0008212 GCST90237306 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High affinity immunoglobulin gamma Fc receptor I level in Chronic kidney disease with hypertension and no diabetes (3312_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 high affinity immunoglobulin gamma fc receptor i measurement http://www.ebi.ac.uk/efo/EFO_0020447 GCST90237307 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDNF family receptor alpha-1 level in Chronic kidney disease with hypertension and no diabetes (3314_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 gdnf family receptor alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020400 GCST90237308 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glypican-2 level in Chronic kidney disease with hypertension and no diabetes (3315_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 glypican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020414 GCST90237309 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparin cofactor 2 level in Chronic kidney disease with hypertension and no diabetes (3316_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 heparin cofactor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008150 GCST90237310 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease HTRA2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (3317_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine protease HTRA2, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020723 GCST90237311 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 7 level in Chronic kidney disease with hypertension and no diabetes (3320_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0008161 GCST90237312 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-24 level in Chronic kidney disease with hypertension and no diabetes (3321_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-24 measurement http://www.ebi.ac.uk/efo/EFO_0020502 GCST90237313 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeats and immunoglobulin-like domains protein 3 level in Chronic kidney disease with hypertension and no diabetes (3322_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 leucine-rich repeats and immunoglobulin-like domains protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020534 GCST90237314 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 8 level in Chronic kidney disease with hypertension and no diabetes (3323_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 low-density lipoprotein receptor-related protein 8 measurement http://www.ebi.ac.uk/efo/EFO_0020538 GCST90237315 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-lymphocyte surface antigen Ly-9 level in Chronic kidney disease with hypertension and no diabetes (3324_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 T-lymphocyte surface antigen Ly-9 measurement http://www.ebi.ac.uk/efo/EFO_0008295 GCST90237316 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrilin-2 level in Chronic kidney disease with hypertension and no diabetes (3325_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020555 GCST90237317 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell adhesion molecule 1 level in Chronic kidney disease with hypertension and no diabetes (3326_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 cell adhesion molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0020251 GCST90237318 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin-4 level in Chronic kidney disease with hypertension and no diabetes (3327_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 netrin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020592 GCST90237319 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidoglycan recognition protein 1 level in Chronic kidney disease with hypertension and no diabetes (3329_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptidoglycan recognition protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020624 GCST90237320 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RGM domain family member B level in Chronic kidney disease with hypertension and no diabetes (3331_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 rgm domain family member b measurement http://www.ebi.ac.uk/efo/EFO_0020708 GCST90237321 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemojuvelin level in Chronic kidney disease with hypertension and no diabetes (3332_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 hemojuvelin measurement http://www.ebi.ac.uk/efo/EFO_0008148 GCST90237322 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tissue factor pathway inhibitor level in Chronic kidney disease with hypertension and no diabetes (3336_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 tissue factor pathway inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0007968 GCST90237323 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin-2 level in Chronic kidney disease with hypertension and no diabetes (3339_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90237324 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin-4 level in Chronic kidney disease with hypertension and no diabetes (3340_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 thrombospondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020771 GCST90237325 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase ABL1 level in Chronic kidney disease with hypertension and no diabetes (3341_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase ABL1 measurement http://www.ebi.ac.uk/efo/EFO_0020818 GCST90237326 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Abelson tyrosine-protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (3342_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 Abelson tyrosine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008012 GCST90237327 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aminoacylase-1 level in Chronic kidney disease with hypertension and no diabetes (3343_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 aminoacylase-1 measurement http://www.ebi.ac.uk/efo/EFO_0020141 GCST90237328 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Antithrombin-III level in Chronic kidney disease with hypertension and no diabetes (3344_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 antithrombin-III measurement http://www.ebi.ac.uk/efo/EFO_0020155 GCST90237329 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aurora kinase B level in Chronic kidney disease with hypertension and no diabetes (3346_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 aurora kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020169 GCST90237330 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. beta-adrenergic receptor kinase 1 level in Chronic kidney disease with hypertension and no diabetes (3347_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 beta-adrenergic receptor kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020181 GCST90237331 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 1 level in Chronic kidney disease with hypertension and no diabetes (3348_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 bone morphogenetic protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020184 GCST90237332 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase type II subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3350_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcium/calmodulin-dependent protein kinase type II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020218 GCST90237333 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase type II subunit beta level in Chronic kidney disease with hypertension and no diabetes (3351_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcium/calmodulin-dependent protein kinase type II subunit beta measurement http://www.ebi.ac.uk/efo/EFO_0020219 GCST90237334 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 6 level in Chronic kidney disease with hypertension and no diabetes (3352_80) 466 African American individuals NA Illumina [14870897] (imputed) 1 carbonic anhydrase 6 measurement http://www.ebi.ac.uk/efo/EFO_0008068 GCST90237335 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 7 level in Chronic kidney disease with hypertension and no diabetes (3356_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase 7 measurement http://www.ebi.ac.uk/efo/EFO_0020231 GCST90237336 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 2:Cyclin-A2 complex level in Chronic kidney disease with hypertension and no diabetes (3357_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 cyclin-dependent kinase 2:cyclin-A2 complex measurement http://www.ebi.ac.uk/efo/EFO_0020295 GCST90237337 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 5:Cyclin-dependent kinase 5 activator 1 complex level in Chronic kidney disease with hypertension and no diabetes (3358_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 cyclin-dependent kinase 5:cyclin-dependent kinase 5 activator 1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020296 GCST90237338 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 8:Cyclin-C complex level in Chronic kidney disease with hypertension and no diabetes (3359_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 cyclin-dependent kinase 8:cyclin-c complex measurement http://www.ebi.ac.uk/efo/EFO_0020297 GCST90237339 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase Chk2 level in Chronic kidney disease with hypertension and no diabetes (3360_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase CHK2 measurement http://www.ebi.ac.uk/efo/EFO_0020726 GCST90237340 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 4 member K level in Chronic kidney disease with hypertension and no diabetes (3361_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-type lectin domain family 4 member K measurement http://www.ebi.ac.uk/efo/EFO_0020201 GCST90237341 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UBE2N/UBE2V2 Complex level in Chronic kidney disease with hypertension and no diabetes (21756_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235857 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 22 level in Chronic kidney disease with hypertension and no diabetes (21757_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 22 in blood serum http://purl.obolibrary.org/obo/OBA_2044061 GCST90235858 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sentrin-specific protease 2 level in Chronic kidney disease with hypertension and no diabetes (21758_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sentrin-specific protease 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043440 GCST90235859 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UBP1/WDR48 Complex level in Chronic kidney disease with hypertension and no diabetes (21759_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235860 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-activating enzyme E1 level in Chronic kidney disease with hypertension and no diabetes (21760_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like modifier-activating enzyme 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043980 GCST90235861 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 46 level in Chronic kidney disease with hypertension and no diabetes (21761_213) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 46 in blood serum http://purl.obolibrary.org/obo/OBA_2044066 GCST90235862 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 11 level in Chronic kidney disease with hypertension and no diabetes (21762_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 11 in blood serum http://purl.obolibrary.org/obo/OBA_2044054 GCST90235863 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 4 level in Chronic kidney disease with hypertension and no diabetes (21763_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044065 GCST90235864 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 30 level in Chronic kidney disease with hypertension and no diabetes (21764_99) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ubiquitin carboxyl-terminal hydrolase 30 in blood serum http://purl.obolibrary.org/obo/OBA_2044064 GCST90235865 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase CYLD level in Chronic kidney disease with hypertension and no diabetes (21765_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ubiquitin carboxyl-terminal hydrolase CYLD in blood serum http://purl.obolibrary.org/obo/OBA_2044613 GCST90235866 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-sulphoglucosamine sulphohydrolase level in Chronic kidney disease with hypertension and no diabetes (21766_50) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of N-sulphoglucosamine sulphohydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2043486 GCST90235867 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 14 level in Chronic kidney disease with hypertension and no diabetes (21767_129) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of polypeptide N-acetylgalactosaminyltransferase 14 in blood serum http://purl.obolibrary.org/obo/OBA_2041663 GCST90235868 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A level in Chronic kidney disease with hypertension and no diabetes (21768_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A in blood serum http://purl.obolibrary.org/obo/OBA_2042362 GCST90235869 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Xylulose kinase level in Chronic kidney disease with hypertension and no diabetes (21769_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of xylulose kinase in blood serum http://purl.obolibrary.org/obo/OBA_2044155 GCST90235870 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (21770_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040300 GCST90235871 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase level in Chronic kidney disease with hypertension and no diabetes (21771_47) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042358 GCST90235872 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein ABHD4 level in Chronic kidney disease with hypertension and no diabetes (21780_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of (lyso)-N-acylphosphatidylethanolamine lipase in blood serum http://purl.obolibrary.org/obo/OBA_2040460 GCST90235873 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartoacylase-2 level in Chronic kidney disease with hypertension and no diabetes (21781_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of N-acyl-aromatic-L-amino acid amidohydrolase, carboxylate-forming in blood serum http://purl.obolibrary.org/obo/OBA_2040492 GCST90235874 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase-like 2 level in Chronic kidney disease with hypertension and no diabetes (21786_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040969 GCST90235875 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FGFR1 oncogene partner level in Chronic kidney disease with hypertension and no diabetes (21793_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centrosomal protein 43 in blood serum http://purl.obolibrary.org/obo/OBA_2041577 GCST90235876 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione peroxidase 3 level in Chronic kidney disease with hypertension and no diabetes (21796_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione peroxidase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041779 GCST90235877 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HLA-C level in Chronic kidney disease with hypertension and no diabetes (21797_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MHC class I histocompatibility antigen C alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040363 GCST90235878 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homer protein homolog 3 level in Chronic kidney disease with hypertension and no diabetes (21799_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homer protein homolog 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041914 GCST90235879 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative KHDC1-like protein level in Chronic kidney disease with hypertension and no diabetes (21804_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235880 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MART-1 level in Chronic kidney disease with hypertension and no diabetes (21810_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma antigen recognized by T-cells 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042375 GCST90235881 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly [ADP-ribose] polymerase 1 level in Chronic kidney disease with hypertension and no diabetes (10534_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232904 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD99 antigen-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (10539_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD99 molecule-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040949 GCST90232905 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin-type laminin G domain and EAR repeat-containing protein level in Chronic kidney disease with hypertension and no diabetes (10546_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein TSPEAR in blood serum http://purl.obolibrary.org/obo/OBA_2043950 GCST90232906 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein receptor type-1B level in Chronic kidney disease with hypertension and no diabetes (10550_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BMP receptor type-1B in blood serum http://purl.obolibrary.org/obo/OBA_2040185 GCST90232907 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Linker for activation of T-cells family member 1 level in Chronic kidney disease with hypertension and no diabetes (10551_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of linker for activation of T-cells family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042167 GCST90232908 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2-F type II integral membrane protein level in Chronic kidney disease with hypertension and no diabetes (10552_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NKG2-F type II integral membrane protein in blood serum http://purl.obolibrary.org/obo/OBA_2042130 GCST90232909 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Torsin-1A-interacting protein 2 level in Chronic kidney disease with hypertension and no diabetes (10553_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 torsin-1A-interacting protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0803160 GCST90232910 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testis-expressed sequence 29 protein level in Chronic kidney disease with hypertension and no diabetes (10557_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of testis-expressed protein 29 in blood serum http://purl.obolibrary.org/obo/OBA_2044394 GCST90232911 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin-9 level in Chronic kidney disease with hypertension and no diabetes (10558_26) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protocadherin-9 in blood serum http://purl.obolibrary.org/obo/OBA_2042784 GCST90232912 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integral membrane protein 2C level in Chronic kidney disease with hypertension and no diabetes (10560_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232913 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidoglycan recognition protein 3 level in Chronic kidney disease with hypertension and no diabetes (10561_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidoglycan recognition protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042863 GCST90232914 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropilin and tolloid-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (10562_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuropilin and tolloid-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042563 GCST90232915 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LysM and putative peptidoglycan-binding domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (10563_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LysM and putative peptidoglycan-binding domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044330 GCST90232916 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT and NTRK-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (10565_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLIT and NTRK-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043548 GCST90232917 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microfibrillar-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (10569_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microfibrillar-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042349 GCST90232918 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase level in Chronic kidney disease with hypertension and no diabetes (10571_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042356 GCST90232919 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-8 level in Chronic kidney disease with hypertension and no diabetes (10572_65) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cystatin-8 in blood serum http://purl.obolibrary.org/obo/OBA_2041176 GCST90232920 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-2-microglobulin level in Chronic kidney disease with hypertension and no diabetes (10574_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 beta-2-microglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020180 GCST90232921 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly(U)-binding-splicing factor PUF60 level in Chronic kidney disease with hypertension and no diabetes (10575_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of poly(U)-binding-splicing factor PUF60 in blood serum http://purl.obolibrary.org/obo/OBA_2043115 GCST90232922 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (10576_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232923 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Surfactant-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (10580_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of surfactant-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043481 GCST90232924 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (10584_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042546 GCST90232925 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactosylceramide alpha-2,3-sialyltransferase level in Chronic kidney disease with hypertension and no diabetes (10588_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lactosylceramide alpha-2,3-sialyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043671 GCST90232926 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoic acid early transcript 1L protein level in Chronic kidney disease with hypertension and no diabetes (10589_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UL16-binding protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043185 GCST90232927 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histatin-3 level in Chronic kidney disease with hypertension and no diabetes (10603_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histatin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041958 GCST90232928 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pulmonary surfactant-associated protein B level in Chronic kidney disease with hypertension and no diabetes (10672_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90232954 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell lectin-like receptor subfamily G member 2 level in Chronic kidney disease with hypertension and no diabetes (10693_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232955 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein WFDC10B level in Chronic kidney disease with hypertension and no diabetes (10695_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein WFDC10B in blood serum http://purl.obolibrary.org/obo/OBA_2044131 GCST90232956 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolow-density lipoprotein receptor-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (10699_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040381 GCST90232957 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily member 11 level in Chronic kidney disease with hypertension and no diabetes (10700_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232958 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(XXVIII) chain level in Chronic kidney disease with hypertension and no diabetes (10702_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 collagen alpha-1(XXIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020270 GCST90232959 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphoid-restricted membrane protein level in Chronic kidney disease with hypertension and no diabetes (10704_91) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol 1,4,5-triphosphate receptor associated 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042227 GCST90232960 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (10705_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043677 GCST90232961 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. F-box only protein 3 level in Chronic kidney disease with hypertension and no diabetes (14628_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of F-box only protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041558 GCST90234276 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 16 level in Chronic kidney disease with hypertension and no diabetes (14631_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 16 in blood serum http://purl.obolibrary.org/obo/OBA_2041381 GCST90234277 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 185A level in Chronic kidney disease with hypertension and no diabetes (14633_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 185A in blood serum http://purl.obolibrary.org/obo/OBA_2044445 GCST90234278 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lutropin-choriogonadotropic hormone receptor level in Chronic kidney disease with hypertension and no diabetes (14634_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lutropin-choriogonadotropic hormone receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040313 GCST90234279 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease UK114 level in Chronic kidney disease with hypertension and no diabetes (14636_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 2-iminobutanoate/2-iminopropanoate deaminase in blood serum http://purl.obolibrary.org/obo/OBA_2041928 GCST90234280 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase A4 level in Chronic kidney disease with hypertension and no diabetes (14645_253) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase A4 in blood serum http://purl.obolibrary.org/obo/OBA_2041804 GCST90234281 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 17 level in Chronic kidney disease with hypertension and no diabetes (14655_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 17 in blood serum http://purl.obolibrary.org/obo/OBA_2044283 GCST90234282 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myeloid zinc finger 1 level in Chronic kidney disease with hypertension and no diabetes (14662_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myeloid zinc finger 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042492 GCST90234283 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF8 level in Chronic kidney disease with hypertension and no diabetes (14663_44) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of E3 ubiquitin-protein ligase RNF8 in blood serum http://purl.obolibrary.org/obo/OBA_2043300 GCST90234284 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ski-like protein level in Chronic kidney disease with hypertension and no diabetes (14670_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ski-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2043519 GCST90234285 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C and casein kinase substrate in neurons protein 3 level in Chronic kidney disease with hypertension and no diabetes (14674_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein kinase C and casein kinase substrate in neurons protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044338 GCST90234286 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4B level in Chronic kidney disease with hypertension and no diabetes (14675_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 4B in blood serum http://purl.obolibrary.org/obo/OBA_2041451 GCST90234287 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpain-2 catalytic subunit level in Chronic kidney disease with hypertension and no diabetes (14684_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calpain-2 catalytic subunit in blood serum http://purl.obolibrary.org/obo/OBA_2040889 GCST90234288 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RAC-beta serine/threonine-protein kinase level in Chronic kidney disease with hypertension and no diabetes (14685_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 RAC-beta serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021989 GCST90234289 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Perilipin-3 level in Chronic kidney disease with hypertension and no diabetes (14687_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of perilipin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042256 GCST90234290 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 7 level in Chronic kidney disease with hypertension and no diabetes (14688_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein phosphatase non-receptor type 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043103 GCST90234291 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein SEC13 homolog level in Chronic kidney disease with hypertension and no diabetes (14689_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein SEC13 in blood serum http://purl.obolibrary.org/obo/OBA_2043417 GCST90234292 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelin-3 level in Chronic kidney disease with hypertension and no diabetes (15383_200) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of endothelin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041415 GCST90234343 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Klotho level in Chronic kidney disease with hypertension and no diabetes (15384_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of klotho in blood serum http://purl.obolibrary.org/obo/OBA_2042114 GCST90234344 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein, intestinal level in Chronic kidney disease with hypertension and no diabetes (15385_116) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of fatty acid-binding protein, intestinal in blood serum http://purl.obolibrary.org/obo/OBA_2041538 GCST90234345 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein, adipocyte level in Chronic kidney disease with hypertension and no diabetes (15386_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 fatty acid-binding protein, adipocyte measurement http://www.ebi.ac.uk/efo/EFO_0010914 GCST90234346 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropilin-2 level in Chronic kidney disease with hypertension and no diabetes (15387_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuropilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042642 GCST90234347 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low affinity immunoglobulin gamma Fc region receptor III-A level in Chronic kidney disease with hypertension and no diabetes (15388_24) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of low affinity immunoglobulin gamma Fc region receptor III-A in blood serum http://purl.obolibrary.org/obo/OBA_2040305 GCST90234348 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frataxin, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (15389_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frataxin, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041637 GCST90234349 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth arrest-specific protein 6 level in Chronic kidney disease with hypertension and no diabetes (15391_114) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth arrest-specific protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041674 GCST90234350 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5B level in Chronic kidney disease with hypertension and no diabetes (15394_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of netrin receptor UNC5B in blood serum http://purl.obolibrary.org/obo/OBA_2044038 GCST90234351 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase Mu 1 level in Chronic kidney disease with hypertension and no diabetes (15395_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutathione S-transferase mu 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041806 GCST90234352 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FAD-linked sulfhydryl oxidase ALR level in Chronic kidney disease with hypertension and no diabetes (15398_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of FAD-linked sulfhydryl oxidase ALR in blood serum http://purl.obolibrary.org/obo/OBA_2041704 GCST90234353 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-binding protein inhibitor ID-1 level in Chronic kidney disease with hypertension and no diabetes (15402_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-binding protein inhibitor ID-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040186 GCST90234354 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-binding protein inhibitor ID-2 level in Chronic kidney disease with hypertension and no diabetes (15403_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-binding protein inhibitor ID-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040187 GCST90234355 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-21 level in Chronic kidney disease with hypertension and no diabetes (15404_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-21 in blood serum http://purl.obolibrary.org/obo/OBA_2041978 GCST90234356 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-4 level in Chronic kidney disease with hypertension and no diabetes (15405_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041979 GCST90234357 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Baculoviral IAP repeat-containing protein 7 level in Chronic kidney disease with hypertension and no diabetes (15412_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of baculoviral IAP repeat-containing protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040416 GCST90234358 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylcholine-sterol acyltransferase level in Chronic kidney disease with hypertension and no diabetes (15413_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylcholine-sterol acyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042169 GCST90234359 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. L-lactate dehydrogenase A chain level in Chronic kidney disease with hypertension and no diabetes (15414_316) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of L-lactate dehydrogenase A chain in blood serum http://purl.obolibrary.org/obo/OBA_2042181 GCST90234360 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin B5 level in Chronic kidney disease with hypertension and no diabetes (15417_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin B5 in blood serum http://purl.obolibrary.org/obo/OBA_2043462 GCST90234361 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 10 level in Chronic kidney disease with hypertension and no diabetes (15418_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042293 GCST90234362 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-20 level in Chronic kidney disease with hypertension and no diabetes (15419_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of matrix metalloproteinase-20 in blood serum http://purl.obolibrary.org/obo/OBA_2042389 GCST90234363 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialidase-1 level in Chronic kidney disease with hypertension and no diabetes (15426_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sialidase-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042564 GCST90234364 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysyl oxidase homolog 3 level in Chronic kidney disease with hypertension and no diabetes (15427_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysyl oxidase homolog 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042220 GCST90234365 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ornithine carbamoyltransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (15431_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ornithine transcarbamylase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042719 GCST90234366 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Otoraplin level in Chronic kidney disease with hypertension and no diabetes (15432_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of otoraplin in blood serum http://purl.obolibrary.org/obo/OBA_2042720 GCST90234367 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adipocyte plasma membrane-associated protein level in Chronic kidney disease with hypertension and no diabetes (10605_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adipocyte plasma membrane-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2040619 GCST90232929 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Torsin-1A-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (10606_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232930 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histatin-1 level in Chronic kidney disease with hypertension and no diabetes (10608_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histatin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041957 GCST90232931 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 level in Chronic kidney disease with hypertension and no diabetes (10612_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 in blood serum http://purl.obolibrary.org/obo/OBA_2042930 GCST90232932 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein CASC4 level in Chronic kidney disease with hypertension and no diabetes (10613_33) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein GOLM2 in blood serum http://purl.obolibrary.org/obo/OBA_2040903 GCST90232933 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myelin protein P0 level in Chronic kidney disease with hypertension and no diabetes (10615_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myelin P0 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042409 GCST90232934 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Podocalyxin-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (10616_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of podocalyxin-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042957 GCST90232935 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (10618_190) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor-related protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042231 GCST90232936 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-microseminoprotein level in Chronic kidney disease with hypertension and no diabetes (10620_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 beta-microseminoprotein measurement http://www.ebi.ac.uk/efo/EFO_0020955 GCST90232937 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Largen level in Chronic kidney disease with hypertension and no diabetes (10621_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Largen in blood serum http://purl.obolibrary.org/obo/OBA_2043044 GCST90232938 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mucin-1 level in Chronic kidney disease with hypertension and no diabetes (10623_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90232939 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 13 level in Chronic kidney disease with hypertension and no diabetes (10624_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine protease inhibitor Kazal-type 13 in blood serum http://purl.obolibrary.org/obo/OBA_2043633 GCST90232940 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (10626_116) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043677 GCST90232941 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (10627_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of amyloid beta precursor like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040618 GCST90232942 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxidoreductase HTATIP2 level in Chronic kidney disease with hypertension and no diabetes (10630_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxidoreductase HTATIP2 in blood serum http://purl.obolibrary.org/obo/OBA_2041956 GCST90232943 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane-associated progesterone receptor component 2 level in Chronic kidney disease with hypertension and no diabetes (10631_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane-associated progesterone receptor component 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042870 GCST90232944 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell surface glycoprotein CD200 receptor 1 level in Chronic kidney disease with hypertension and no diabetes (10636_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 cell surface glycoprotein CD200 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020253 GCST90232945 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0577 protein KIAA1324 level in Chronic kidney disease with hypertension and no diabetes (10637_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232946 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TERF1-interacting nuclear factor 2 level in Chronic kidney disease with hypertension and no diabetes (10638_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TERF1-interacting nuclear factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043858 GCST90232947 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noelin-3 level in Chronic kidney disease with hypertension and no diabetes (10643_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232948 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activating signal cointegrator 1 complex subunit 1 level in Chronic kidney disease with hypertension and no diabetes (10647_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activating signal cointegrator 1 complex subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040694 GCST90232949 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-induced gene 1 protein level in Chronic kidney disease with hypertension and no diabetes (10663_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-induced gene 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042033 GCST90232950 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylglucosamine-1-phosphotransferase subunit gamma level in Chronic kidney disease with hypertension and no diabetes (10666_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetylglucosamine-1-phosphotransferase subunit gamma in blood serum http://purl.obolibrary.org/obo/OBA_2041758 GCST90232951 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C1orf185 level in Chronic kidney disease with hypertension and no diabetes (10667_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C1orf185 in blood serum http://purl.obolibrary.org/obo/OBA_2044830 GCST90232952 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-4 level in Chronic kidney disease with hypertension and no diabetes (10668_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043715 GCST90232953 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proto-oncogene tyrosine-protein kinase Src level in Chronic kidney disease with hypertension and no diabetes (15433_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 proto-oncogene tyrosine-protein kinase Src measurement http://www.ebi.ac.uk/efo/EFO_0010927 GCST90234368 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prepronociceptin level in Chronic kidney disease with hypertension and no diabetes (15434_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nociceptin in blood serum http://purl.obolibrary.org/obo/OBA_2042953 GCST90234369 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Purine nucleoside phosphorylase level in Chronic kidney disease with hypertension and no diabetes (15435_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of purine nucleoside phosphorylase in blood serum http://purl.obolibrary.org/obo/OBA_2042611 GCST90234370 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor activity-modifying protein 1 level in Chronic kidney disease with hypertension and no diabetes (15436_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor activity-modifying protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043188 GCST90234371 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Very Late Antigen-4 level in Chronic kidney disease with hypertension and no diabetes (21688_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235811 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (21690_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044415 GCST90235812 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and fibronectin type-III domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (21691_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and fibronectin type-III domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044486 GCST90235813 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD8A/CD8B Complex level in Chronic kidney disease with hypertension and no diabetes (21692_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235814 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-13 level in Chronic kidney disease with hypertension and no diabetes (21693_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-13 in blood serum http://purl.obolibrary.org/obo/OBA_2040958 GCST90235815 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and fibronectin type-III domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (21696_80) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leucine-rich repeat and fibronectin type-III domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044328 GCST90235816 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G-protein coupled receptor F2 level in Chronic kidney disease with hypertension and no diabetes (21697_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adhesion G-protein coupled receptor F2 in blood serum http://purl.obolibrary.org/obo/OBA_2044512 GCST90235817 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin a11b1 level in Chronic kidney disease with hypertension and no diabetes (21698_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235818 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin-12 level in Chronic kidney disease with hypertension and no diabetes (21704_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protocadherin-12 in blood serum http://purl.obolibrary.org/obo/OBA_2042780 GCST90235819 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Meteorin-like protein level in Chronic kidney disease with hypertension and no diabetes (21705_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of meteorin-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042343 GCST90235820 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily A member 1 level in Chronic kidney disease with hypertension and no diabetes (21706_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily A member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042194 GCST90235821 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (21707_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040847 GCST90235822 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IgG receptor FcRn large subunit p51 level in Chronic kidney disease with hypertension and no diabetes (21708_149) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of IgG receptor FcRn large subunit p51 in blood serum http://purl.obolibrary.org/obo/OBA_2041562 GCST90235823 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-4, Y-linked level in Chronic kidney disease with hypertension and no diabetes (21710_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroligin-4, Y-linked in blood serum http://purl.obolibrary.org/obo/OBA_2042590 GCST90235824 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brain-specific angiogenesis inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (21711_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adhesion G protein-coupled receptor B1 in blood serum http://purl.obolibrary.org/obo/OBA_2040772 GCST90235825 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Reelin level in Chronic kidney disease with hypertension and no diabetes (21713_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of reelin in blood serum http://purl.obolibrary.org/obo/OBA_2043237 GCST90235826 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sentrin-specific protease 1 level in Chronic kidney disease with hypertension and no diabetes (21715_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sentrin-specific protease 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043439 GCST90235827 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-(1,3)-fucosyltransferase level in Chronic kidney disease with hypertension and no diabetes (21716_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-(1,3)-fucosyltransferase 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044450 GCST90235828 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 Q2 level in Chronic kidney disease with hypertension and no diabetes (21717_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 Q2 in blood serum http://purl.obolibrary.org/obo/OBA_2044001 GCST90235829 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hyaluronidase-4 level in Chronic kidney disease with hypertension and no diabetes (21718_150) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hyaluronidase-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041962 GCST90235830 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-(1,3)-fucosyltransferase 11 level in Chronic kidney disease with hypertension and no diabetes (21720_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-(1,3)-fucosyltransferase 11 in blood serum http://purl.obolibrary.org/obo/OBA_2041633 GCST90235831 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 276 level in Chronic kidney disease with hypertension and no diabetes (14692_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of zinc finger protein 276 in blood serum http://purl.obolibrary.org/obo/OBA_2044199 GCST90234293 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptase beta-2 level in Chronic kidney disease with hypertension and no diabetes (14696_45) 466 African American individuals NA Illumina [14870897] (imputed) 1 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90234294 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor D level in Chronic kidney disease with hypertension and no diabetes (14705_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 vascular endothelial growth factor D measurement http://www.ebi.ac.uk/efo/EFO_0010575 GCST90234295 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C8 gamma chain level in Chronic kidney disease with hypertension and no diabetes (14708_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement component C8 gamma chain in blood serum http://purl.obolibrary.org/obo/OBA_2040857 GCST90234296 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-M level in Chronic kidney disease with hypertension and no diabetes (14711_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin-M measurement http://www.ebi.ac.uk/efo/EFO_0020299 GCST90234297 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Azurocidin level in Chronic kidney disease with hypertension and no diabetes (14713_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 azurocidin measurement http://www.ebi.ac.uk/efo/EFO_0020170 GCST90234298 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine receptor-like factor 1 level in Chronic kidney disease with hypertension and no diabetes (14747_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytokine receptor-like factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041147 GCST90234299 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 5 level in Chronic kidney disease with hypertension and no diabetes (14748_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040654 GCST90234300 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactotransferrin level in Chronic kidney disease with hypertension and no diabetes (14755_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 lactotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020526 GCST90234301 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 2 level in Chronic kidney disease with hypertension and no diabetes (14756_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90234302 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-1 level in Chronic kidney disease with hypertension and no diabetes (14759_149) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90234303 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropilin and tolloid-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (15298_199) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuropilin and tolloid-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042562 GCST90234304 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LDLR chaperone MESD level in Chronic kidney disease with hypertension and no diabetes (15299_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mesoderm development candidate 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042342 GCST90234305 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 134 level in Chronic kidney disease with hypertension and no diabetes (15300_66) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of coiled-coil domain-containing protein 134 in blood serum http://purl.obolibrary.org/obo/OBA_2044258 GCST90234306 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A5 level in Chronic kidney disease with hypertension and no diabetes (15303_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A5 in blood serum http://purl.obolibrary.org/obo/OBA_2043368 GCST90234307 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regenerating islet-derived protein 3-alpha level in Chronic kidney disease with hypertension and no diabetes (15304_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regenerating islet-derived protein 3-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043232 GCST90234308 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretagogin level in Chronic kidney disease with hypertension and no diabetes (15305_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretagogin in blood serum http://purl.obolibrary.org/obo/OBA_2043400 GCST90234309 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin J chain level in Chronic kidney disease with hypertension and no diabetes (15306_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin J chain in blood serum http://purl.obolibrary.org/obo/OBA_2041996 GCST90234310 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brorin level in Chronic kidney disease with hypertension and no diabetes (15308_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of brorin in blood serum http://purl.obolibrary.org/obo/OBA_2044121 GCST90234311 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein regulator of cytokinesis 1 level in Chronic kidney disease with hypertension and no diabetes (15310_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein regulator of cytokinesis 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043017 GCST90234312 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein argonaute-1 level in Chronic kidney disease with hypertension and no diabetes (15312_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein argonaute-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041441 GCST90234313 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitotic spindle assembly checkpoint protein MAD2A level in Chronic kidney disease with hypertension and no diabetes (15313_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitotic spindle assembly checkpoint protein MAD2A in blood serum http://purl.obolibrary.org/obo/OBA_2042258 GCST90234314 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chloride intracellular channel protein 4 level in Chronic kidney disease with hypertension and no diabetes (15314_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chloride intracellular channel protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041050 GCST90234315 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Copper homeostasis protein cutC homolog level in Chronic kidney disease with hypertension and no diabetes (15315_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of copper homeostasis protein cutC in blood serum http://purl.obolibrary.org/obo/OBA_2041202 GCST90234316 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin-like protein 4B level in Chronic kidney disease with hypertension and no diabetes (15316_262) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of thioredoxin-like protein 4B in blood serum http://purl.obolibrary.org/obo/OBA_2043973 GCST90234317 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 10 level in Chronic kidney disease with hypertension and no diabetes (21721_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041020 GCST90235832 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 4 level in Chronic kidney disease with hypertension and no diabetes (21722_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of polypeptide N-acetylgalactosaminyltransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041666 GCST90235833 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylgalactosamine-6-sulfatase level in Chronic kidney disease with hypertension and no diabetes (21724_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetylgalactosamine-6-sulfatase in blood serum http://purl.obolibrary.org/obo/OBA_2041658 GCST90235834 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase level in Chronic kidney disease with hypertension and no diabetes (21726_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043678 GCST90235835 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 Q1 level in Chronic kidney disease with hypertension and no diabetes (21727_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 Q1 in blood serum http://purl.obolibrary.org/obo/OBA_2044000 GCST90235836 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 2 level in Chronic kidney disease with hypertension and no diabetes (21728_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044059 GCST90235837 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 19 level in Chronic kidney disease with hypertension and no diabetes (21730_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 19 in blood serum http://purl.obolibrary.org/obo/OBA_2044058 GCST90235838 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 Q1 level in Chronic kidney disease with hypertension and no diabetes (21732_78) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ubiquitin-conjugating enzyme E2 Q1 in blood serum http://purl.obolibrary.org/obo/OBA_2044000 GCST90235839 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (21733_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit in blood serum http://purl.obolibrary.org/obo/OBA_2042697 GCST90235840 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C1GLT/C1GLC Complex level in Chronic kidney disease with hypertension and no diabetes (21734_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235841 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan sulfate 2-O-sulfotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (21736_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heparan sulfate 2-O-sulfotransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041929 GCST90235842 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-galactoside alpha-2,6-sialyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (21737_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of beta-galactoside alpha-2,6-sialyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043674 GCST90235843 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase level in Chronic kidney disease with hypertension and no diabetes (21739_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase in blood serum http://purl.obolibrary.org/obo/OBA_2041751 GCST90235844 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (21740_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044052 GCST90235845 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. OTU domain-containing protein 7B level in Chronic kidney disease with hypertension and no diabetes (21742_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of OTU domain-containing protein 7B in blood serum http://purl.obolibrary.org/obo/OBA_2042722 GCST90235846 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WD repeat-containing protein 48 level in Chronic kidney disease with hypertension and no diabetes (21743_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WD repeat-containing protein 48 in blood serum http://purl.obolibrary.org/obo/OBA_2044127 GCST90235847 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 10 level in Chronic kidney disease with hypertension and no diabetes (21746_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044053 GCST90235848 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UBE2N (Ubc13)/Uev1a Complex level in Chronic kidney disease with hypertension and no diabetes (21747_114) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235849 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UBE2N (Ubc13)/Uev1a Complex level in Chronic kidney disease with hypertension and no diabetes (21747_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235850 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UBP46/WDR48 Complex level in Chronic kidney disease with hypertension and no diabetes (21748_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235851 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase BAP1 level in Chronic kidney disease with hypertension and no diabetes (21750_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase BAP1 in blood serum http://purl.obolibrary.org/obo/OBA_2040776 GCST90235852 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. USP12/WDR48 Complex level in Chronic kidney disease with hypertension and no diabetes (21751_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235853 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial Rho GTPase 1 level in Chronic kidney disease with hypertension and no diabetes (21752_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial Rho GTPase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043269 GCST90235854 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin thioesterase ZRANB1 level in Chronic kidney disease with hypertension and no diabetes (21754_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin thioesterase ZRANB1 in blood serum http://purl.obolibrary.org/obo/OBA_2044220 GCST90235855 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 12 level in Chronic kidney disease with hypertension and no diabetes (21755_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 12 in blood serum http://purl.obolibrary.org/obo/OBA_2044055 GCST90235856 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A10 level in Chronic kidney disease with hypertension and no diabetes (15318_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A10 in blood serum http://purl.obolibrary.org/obo/OBA_2043362 GCST90234318 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-A1 level in Chronic kidney disease with hypertension and no diabetes (15319_226) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-A1 in blood serum http://purl.obolibrary.org/obo/OBA_2040931 GCST90234319 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complexin-2 level in Chronic kidney disease with hypertension and no diabetes (15321_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complexin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041118 GCST90234320 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Death domain-containing protein CRADD level in Chronic kidney disease with hypertension and no diabetes (15322_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of death domain-containing protein CRADD in blood serum http://purl.obolibrary.org/obo/OBA_2041128 GCST90234321 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein argonaute-3 level in Chronic kidney disease with hypertension and no diabetes (15323_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein argonaute-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041443 GCST90234322 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ferritin light chain level in Chronic kidney disease with hypertension and no diabetes (15324_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ferritin light chain in blood serum http://purl.obolibrary.org/obo/OBA_2041626 GCST90234323 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuromodulin level in Chronic kidney disease with hypertension and no diabetes (15325_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuromodulin in blood serum http://purl.obolibrary.org/obo/OBA_2041670 GCST90234324 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylate-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (15326_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanylate-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041680 GCST90234325 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ragulator complex protein LAMTOR2 level in Chronic kidney disease with hypertension and no diabetes (15329_167) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ragulator complex protein LAMTOR2 in blood serum http://purl.obolibrary.org/obo/OBA_2043304 GCST90234326 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal cell-derived factor 2 level in Chronic kidney disease with hypertension and no diabetes (15333_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of stromal cell-derived factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043413 GCST90234327 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Selenoprotein M level in Chronic kidney disease with hypertension and no diabetes (15336_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of selenoprotein M in blood serum http://purl.obolibrary.org/obo/OBA_2043425 GCST90234328 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon gamma level in Chronic kidney disease with hypertension and no diabetes (15346_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon gamma measurement http://www.ebi.ac.uk/efo/EFO_0008165 GCST90234329 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemopexin level in Chronic kidney disease with hypertension and no diabetes (15347_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90234330 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroendocrine protein 7B2 level in Chronic kidney disease with hypertension and no diabetes (15358_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of neuroendocrine protein 7B2 in blood serum http://purl.obolibrary.org/obo/OBA_2043396 GCST90234331 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (15361_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040591 GCST90234332 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein A-V level in Chronic kidney disease with hypertension and no diabetes (15363_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apolipoprotein A-V in blood serum http://purl.obolibrary.org/obo/OBA_2040623 GCST90234333 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein C-I level in Chronic kidney disease with hypertension and no diabetes (15364_101) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of apolipoprotein C-I in blood serum http://purl.obolibrary.org/obo/OBA_2040624 GCST90234334 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G protein-coupled receptor B3 level in Chronic kidney disease with hypertension and no diabetes (15365_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adhesion G protein-coupled receptor B3 in blood serum http://purl.obolibrary.org/obo/OBA_2040774 GCST90234335 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BMP-binding endothelial regulator protein level in Chronic kidney disease with hypertension and no diabetes (15368_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 BMP-binding endothelial regulator protein measurement http://www.ebi.ac.uk/efo/EFO_0020183 GCST90234336 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BolA-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (15370_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of BolA-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040816 GCST90234337 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bromodomain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (15372_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bromodomain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040824 GCST90234338 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastrokine-1 level in Chronic kidney disease with hypertension and no diabetes (15374_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gastrokine-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041724 GCST90234339 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase B level in Chronic kidney disease with hypertension and no diabetes (15375_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase B in blood serum http://purl.obolibrary.org/obo/OBA_2041115 GCST90234340 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin E level in Chronic kidney disease with hypertension and no diabetes (15376_134) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin E measurement http://www.ebi.ac.uk/efo/EFO_0020241 GCST90234341 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Discoidin domain-containing receptor 2 level in Chronic kidney disease with hypertension and no diabetes (15381_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 discoidin domain-containing receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020327 GCST90234342 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Triggering receptor expressed on myeloid cells 2 level in Chronic kidney disease with hypertension and no diabetes (16300_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of triggering receptor expressed on myeloid cells 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043927 GCST90234514 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BPI fold-containing family A member 2 level in Chronic kidney disease with hypertension and no diabetes (16302_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BPI fold-containing family A member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043639 GCST90234515 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing G-protein coupled receptor 4 level in Chronic kidney disease with hypertension and no diabetes (16304_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing G-protein coupled receptor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040310 GCST90234516 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-11 level in Chronic kidney disease with hypertension and no diabetes (16305_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234517 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5D level in Chronic kidney disease with hypertension and no diabetes (16307_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90234518 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B- and T-lymphocyte attenuator level in Chronic kidney disease with hypertension and no diabetes (16308_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of B- and T-lymphocyte attenuator in blood serum http://purl.obolibrary.org/obo/OBA_2040256 GCST90234519 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dickkopf-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (16309_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 dickkopf-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020324 GCST90234520 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-6 level in Chronic kidney disease with hypertension and no diabetes (16312_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020214 GCST90234521 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor receptor 1 level in Chronic kidney disease with hypertension and no diabetes (16315_105) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vascular endothelial growth factor receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041595 GCST90234522 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmoglein-3 level in Chronic kidney disease with hypertension and no diabetes (16317_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of desmoglein-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041369 GCST90234523 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase receptor R3 level in Chronic kidney disease with hypertension and no diabetes (16318_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase receptor R3 measurement http://www.ebi.ac.uk/efo/EFO_0020733 GCST90234524 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD320 antigen level in Chronic kidney disease with hypertension and no diabetes (16320_139) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD320 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040261 GCST90234525 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Marginal zone B- and B1-cell-specific protein level in Chronic kidney disease with hypertension and no diabetes (16322_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proapoptotic caspase adapter protein in blood serum http://purl.obolibrary.org/obo/OBA_2042738 GCST90234526 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexin-3 level in Chronic kidney disease with hypertension and no diabetes (16323_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurexin-3-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2044802 GCST90234527 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 1 level in Chronic kidney disease with hypertension and no diabetes (16324_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234528 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High mobility group protein HMG-I/HMG-Y level in Chronic kidney disease with hypertension and no diabetes (16536_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high mobility group protein HMG-I/HMG-Y in blood serum http://purl.obolibrary.org/obo/OBA_2041887 GCST90234529 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal transducer and activator of transcription 5B level in Chronic kidney disease with hypertension and no diabetes (16551_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal transducer and activator of transcription 5b in blood serum http://purl.obolibrary.org/obo/OBA_2040391 GCST90234530 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myocilin level in Chronic kidney disease with hypertension and no diabetes (16558_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of myocilin in blood serum http://purl.obolibrary.org/obo/OBA_2042488 GCST90234531 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1B-glycoprotein level in Chronic kidney disease with hypertension and no diabetes (16561_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of alpha-1B-glycoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2040448 GCST90234532 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bis(5'-nucleosyl)-tetraphosphatase [asymmetrical] level in Chronic kidney disease with hypertension and no diabetes (16583_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of bis(5'-nucleosyl)-tetraphosphatase [asymmetrical] in blood serum http://purl.obolibrary.org/obo/OBA_2042669 GCST90234533 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4 level in Chronic kidney disease with hypertension and no diabetes (16585_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040752 GCST90234534 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acidic mammalian chitinase level in Chronic kidney disease with hypertension and no diabetes (16591_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acidic mammalian chitinase in blood serum http://purl.obolibrary.org/obo/OBA_2041007 GCST90234535 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FAS-associated death domain protein level in Chronic kidney disease with hypertension and no diabetes (16593_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of FAS-associated death domain protein in blood serum http://purl.obolibrary.org/obo/OBA_2040399 GCST90234536 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fas apoptotic inhibitory molecule 1 level in Chronic kidney disease with hypertension and no diabetes (16594_44) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Fas apoptotic inhibitory molecule 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041545 GCST90234537 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaredoxin-3 level in Chronic kidney disease with hypertension and no diabetes (16596_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutaredoxin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041734 GCST90234538 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin beta-7 level in Chronic kidney disease with hypertension and no diabetes (11205_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin beta-7 in blood serum http://purl.obolibrary.org/obo/OBA_2042054 GCST90233125 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage scavenger receptor types I and II level in Chronic kidney disease with hypertension and no diabetes (11207_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90233126 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase level in Chronic kidney disease with hypertension and no diabetes (11208_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase in blood serum http://purl.obolibrary.org/obo/OBA_2042501 GCST90233127 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin-specific chaperone E level in Chronic kidney disease with hypertension and no diabetes (11211_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin-specific chaperone E in blood serum http://purl.obolibrary.org/obo/OBA_2043792 GCST90233128 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin domain-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (11212_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thioredoxin domain-containing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043969 GCST90233129 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 9 level in Chronic kidney disease with hypertension and no diabetes (11214_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 9 in blood serum http://purl.obolibrary.org/obo/OBA_2041329 GCST90233130 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-15 level in Chronic kidney disease with hypertension and no diabetes (11215_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0020211 GCST90233131 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thiopurine S-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (11218_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thiopurine S-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043912 GCST90233132 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (11219_95) 466 African American individuals NA Illumina [14870897] (imputed) 1 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90233133 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C10orf105 level in Chronic kidney disease with hypertension and no diabetes (11220_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C10orf105 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044915 GCST90233134 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 154 level in Chronic kidney disease with hypertension and no diabetes (11223_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 154 in blood serum http://purl.obolibrary.org/obo/OBA_2044369 GCST90233135 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-protein ligase E3A level in Chronic kidney disease with hypertension and no diabetes (11226_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-protein ligase E3A in blood serum http://purl.obolibrary.org/obo/OBA_2044007 GCST90233136 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transducin beta-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (11227_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transducin beta-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043794 GCST90233137 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein RIC-3 level in Chronic kidney disease with hypertension and no diabetes (11228_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein RIC-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043271 GCST90233138 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase/endoribonuclease IRE1 level in Chronic kidney disease with hypertension and no diabetes (11229_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase/endoribonuclease IRE1 in blood serum http://purl.obolibrary.org/obo/OBA_2041507 GCST90233139 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adrenodoxin-like protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11231_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ferredoxin-2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041570 GCST90233140 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcobalamin-1 level in Chronic kidney disease with hypertension and no diabetes (11232_46) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transcobalamin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043815 GCST90233141 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Procollagen C-endopeptidase enhancer 1 level in Chronic kidney disease with hypertension and no diabetes (11237_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of procollagen C-endopeptidase enhancer 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042802 GCST90233142 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protease serine 6 level in Chronic kidney disease with hypertension and no diabetes (11239_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transmembrane protease serine 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043885 GCST90233143 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Argininosuccinate lyase level in Chronic kidney disease with hypertension and no diabetes (11241_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of argininosuccinate lyase in blood serum http://purl.obolibrary.org/obo/OBA_2040701 GCST90233144 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-glutamine gamma-glutamyltransferase K level in Chronic kidney disease with hypertension and no diabetes (11242_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-glutamine gamma-glutamyltransferase K in blood serum http://purl.obolibrary.org/obo/OBA_2043838 GCST90233145 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G-protein coupled receptor F1 level in Chronic kidney disease with hypertension and no diabetes (11243_90) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of adhesion G-protein coupled receptor F1 in blood serum http://purl.obolibrary.org/obo/OBA_2044476 GCST90233146 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Filamin-A level in Chronic kidney disease with hypertension and no diabetes (11245_43) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233147 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BPI fold-containing family B member 1 level in Chronic kidney disease with hypertension and no diabetes (11246_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BPI fold-containing family B member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042224 GCST90233148 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylglutamate synthase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11247_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetylglutamate synthase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042502 GCST90233149 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Teneurin-2 level in Chronic kidney disease with hypertension and no diabetes (11164_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of teneurin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042692 GCST90233100 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myotubularin-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (11167_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myotubularin-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042452 GCST90233101 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Multiple epidermal growth factor-like domains protein 10 level in Chronic kidney disease with hypertension and no diabetes (11168_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of multiple epidermal growth factor-like domains protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042332 GCST90233102 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Filamin-A level in Chronic kidney disease with hypertension and no diabetes (11171_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233103 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Allergin-1 level in Chronic kidney disease with hypertension and no diabetes (11173_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of allergin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044633 GCST90233104 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin type-1 domain-containing protein 7A level in Chronic kidney disease with hypertension and no diabetes (11174_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233105 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysophosphatidylcholine acyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (11175_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysophosphatidylcholine acyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042221 GCST90233106 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type II cytoskeletal 5 level in Chronic kidney disease with hypertension and no diabetes (11177_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type II cytoskeletal 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042144 GCST90233107 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (11178_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233108 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testis-specific serine/threonine-protein kinase 1 level in Chronic kidney disease with hypertension and no diabetes (11179_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of testis-specific serine/threonine-protein kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043952 GCST90233109 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SWI/SNF complex subunit SMARCC1 level in Chronic kidney disease with hypertension and no diabetes (11180_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SWI/SNF complex subunit SMARCC1 in blood serum http://purl.obolibrary.org/obo/OBA_2043553 GCST90233110 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP cyclohydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (11185_145) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP cyclohydrolase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041686 GCST90233111 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 52 level in Chronic kidney disease with hypertension and no diabetes (11186_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 52 in blood serum http://purl.obolibrary.org/obo/OBA_2044431 GCST90233112 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 12 member A level in Chronic kidney disease with hypertension and no diabetes (11187_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of C-type lectin domain family 12 member A in blood serum http://purl.obolibrary.org/obo/OBA_2041043 GCST90233113 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent zinc metalloprotease YME1L1 level in Chronic kidney disease with hypertension and no diabetes (11190_129) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent zinc metalloprotease YME1L1 in blood serum http://purl.obolibrary.org/obo/OBA_2044164 GCST90233114 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulointerstitial nephritis antigen-like level in Chronic kidney disease with hypertension and no diabetes (11192_168) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulointerstitial nephritis antigen-like in blood serum http://purl.obolibrary.org/obo/OBA_2043857 GCST90233115 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte nuclear factor 1-alpha level in Chronic kidney disease with hypertension and no diabetes (11193_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatocyte nuclear factor 1-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041900 GCST90233116 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signaling threshold-regulating transmembrane adapter 1 level in Chronic kidney disease with hypertension and no diabetes (11194_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signaling threshold-regulating transmembrane adapter 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043516 GCST90233117 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-3(VI) chain level in Chronic kidney disease with hypertension and no diabetes (11196_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233118 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-responsive element-binding protein 3-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (11198_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-responsive element-binding protein 3-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041132 GCST90233119 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C1q receptor level in Chronic kidney disease with hypertension and no diabetes (11200_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement component C1q receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040369 GCST90233120 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA pseudouridine synthase A, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11201_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic tRNA pseudouridine synthase A in blood serum http://purl.obolibrary.org/obo/OBA_2043118 GCST90233121 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-box transcription factor TBX5 level in Chronic kidney disease with hypertension and no diabetes (11202_70) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of T-box transcription factor TBX5 in blood serum http://purl.obolibrary.org/obo/OBA_2043798 GCST90233122 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyruvate kinase PKLR level in Chronic kidney disease with hypertension and no diabetes (11203_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyruvate kinase PKLR in blood serum http://purl.obolibrary.org/obo/OBA_2042906 GCST90233123 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coxsackievirus and adenovirus receptor level in Chronic kidney disease with hypertension and no diabetes (11204_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coxsackievirus and adenovirus receptor in blood serum http://purl.obolibrary.org/obo/OBA_2041205 GCST90233124 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uroporphyrinogen-III synthase level in Chronic kidney disease with hypertension and no diabetes (11248_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uroporphyrinogen-III synthase in blood serum http://purl.obolibrary.org/obo/OBA_2044047 GCST90233150 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and calponin homology domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (11252_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233151 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Papilin level in Chronic kidney disease with hypertension and no diabetes (11254_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of papilin in blood serum http://purl.obolibrary.org/obo/OBA_2042758 GCST90233152 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydropteridine reductase level in Chronic kidney disease with hypertension and no diabetes (11257_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydropteridine reductase in blood serum http://purl.obolibrary.org/obo/OBA_2043129 GCST90233153 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily B member 3 level in Chronic kidney disease with hypertension and no diabetes (15615_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte immunoglobulin-like receptor subfamily B member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042199 GCST90234468 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine SCM-1 beta level in Chronic kidney disease with hypertension and no diabetes (15617_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytokine SCM-1 beta in blood serum http://purl.obolibrary.org/obo/OBA_2040392 GCST90234469 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myelin-oligodendrocyte glycoprotein level in Chronic kidney disease with hypertension and no diabetes (15619_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myelin-oligodendrocyte glycoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2042400 GCST90234470 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-1 level in Chronic kidney disease with hypertension and no diabetes (15620_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroligin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042588 GCST90234471 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Opioid-binding protein/cell adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (15622_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 opioid-binding protein/cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020618 GCST90234472 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death protein 1 level in Chronic kidney disease with hypertension and no diabetes (15623_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of programmed cell death protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040355 GCST90234473 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Basement membrane-specific heparan sulfate proteoglycan core protein level in Chronic kidney disease with hypertension and no diabetes (15626_223) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of basement membrane-specific heparan sulfate proteoglycan core protein in blood serum http://purl.obolibrary.org/obo/OBA_2041954 GCST90234474 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RAC-alpha serine/threonine-protein kinase level in Chronic kidney disease with hypertension and no diabetes (15627_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RAC-alpha serine/threonine-protein kinase in blood serum http://purl.obolibrary.org/obo/OBA_2040400 GCST90234475 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 1 level in Chronic kidney disease with hypertension and no diabetes (15631_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pregnancy-specific beta-1-glycoprotein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043055 GCST90234476 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (15633_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 retinol-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020707 GCST90234477 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Slit homolog 1 protein level in Chronic kidney disease with hypertension and no diabetes (15634_139) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of slit homolog 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043544 GCST90234478 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPARC-related modular calcium-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (15635_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SPARC-related modular calcium-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043557 GCST90234479 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. VPS10 domain-containing receptor SorCS1 level in Chronic kidney disease with hypertension and no diabetes (15636_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of VPS10 domain-containing receptor SorCS1 in blood serum http://purl.obolibrary.org/obo/OBA_2044726 GCST90234480 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. VPS10 domain-containing receptor SorCS3 level in Chronic kidney disease with hypertension and no diabetes (15637_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of VPS10 domain-containing receptor SorCS3 in blood serum http://purl.obolibrary.org/obo/OBA_2044491 GCST90234481 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transgelin level in Chronic kidney disease with hypertension and no diabetes (15640_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transgelin in blood serum http://purl.obolibrary.org/obo/OBA_2043772 GCST90234482 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tomoregulin-1 level in Chronic kidney disease with hypertension and no diabetes (15641_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tomoregulin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043870 GCST90234483 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biotinidase level in Chronic kidney disease with hypertension and no diabetes (15644_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of biotinidase in blood serum http://purl.obolibrary.org/obo/OBA_2040831 GCST90234484 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(X) chain level in Chronic kidney disease with hypertension and no diabetes (15653_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of collagen alpha-1(X) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041080 GCST90234485 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 2 level in Chronic kidney disease with hypertension and no diabetes (15666_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040204 GCST90234486 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 4 level in Chronic kidney disease with hypertension and no diabetes (15667_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040205 GCST90234487 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 8B level in Chronic kidney disease with hypertension and no diabetes (15668_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 8B in blood serum http://purl.obolibrary.org/obo/OBA_2040207 GCST90234488 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase B-raf level in Chronic kidney disease with hypertension and no diabetes (15669_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-Raf proto-oncogene serine/threonine-protein kinase in blood serum http://purl.obolibrary.org/obo/OBA_2040823 GCST90234489 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (15670_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of complement C1q-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040846 GCST90234490 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell antigen receptor complex-associated protein alpha chain level in Chronic kidney disease with hypertension and no diabetes (15674_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell antigen receptor complex-associated protein alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040257 GCST90234491 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CCAAT/enhancer-binding protein beta level in Chronic kidney disease with hypertension and no diabetes (15675_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 CCAAT/enhancer-binding protein beta measurement http://www.ebi.ac.uk/efo/EFO_0021905 GCST90234492 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin beta C chain level in Chronic kidney disease with hypertension and no diabetes (15686_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of activin/inhibin beta C chain in blood serum http://purl.obolibrary.org/obo/OBA_2040211 GCST90234493 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein ERGIC-53 level in Chronic kidney disease with hypertension and no diabetes (15688_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein ERGIC-53 in blood serum http://purl.obolibrary.org/obo/OBA_2042210 GCST90234494 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nodal homolog level in Chronic kidney disease with hypertension and no diabetes (15692_300) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nodal protein in blood serum http://purl.obolibrary.org/obo/OBA_2040195 GCST90234495 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Progesterone receptor level in Chronic kidney disease with hypertension and no diabetes (15693_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of progesterone receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042868 GCST90234496 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-taxilin level in Chronic kidney disease with hypertension and no diabetes (15698_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-taxilin in blood serum http://purl.obolibrary.org/obo/OBA_2040265 GCST90234497 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alanine aminotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (16015_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90234498 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor receptor 3 level in Chronic kidney disease with hypertension and no diabetes (16035_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90234499 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SHC-transforming protein 1 level in Chronic kidney disease with hypertension and no diabetes (16043_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 shc-transforming protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020738 GCST90234500 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H-related protein 5 level in Chronic kidney disease with hypertension and no diabetes (16055_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90234501 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cation-independent mannose-6-phosphate receptor level in Chronic kidney disease with hypertension and no diabetes (16057_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90234502 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nidogen-2 level in Chronic kidney disease with hypertension and no diabetes (16060_99) 466 African American individuals NA Illumina [14870897] (imputed) 1 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90234503 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Wnt inhibitory factor 1 level in Chronic kidney disease with hypertension and no diabetes (16070_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 wnt inhibitory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020853 GCST90234504 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRB2-related adapter protein 2 level in Chronic kidney disease with hypertension and no diabetes (16074_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90234505 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase Tec level in Chronic kidney disease with hypertension and no diabetes (16079_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase TEC measurement http://www.ebi.ac.uk/efo/EFO_0020830 GCST90234506 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldo-keto reductase family 1 member B10 level in Chronic kidney disease with hypertension and no diabetes (16081_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member B10 in blood serum http://purl.obolibrary.org/obo/OBA_2040548 GCST90234507 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 4 level in Chronic kidney disease with hypertension and no diabetes (16288_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ephrin type-A receptor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041489 GCST90234508 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastric inhibitory polypeptide level in Chronic kidney disease with hypertension and no diabetes (16292_288) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gastric inhibitory polypeptide in blood serum http://purl.obolibrary.org/obo/OBA_2041720 GCST90234509 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Somatoliberin level in Chronic kidney disease with hypertension and no diabetes (16293_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of somatoliberin in blood serum http://purl.obolibrary.org/obo/OBA_2041715 GCST90234510 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing G-protein coupled receptor 5 level in Chronic kidney disease with hypertension and no diabetes (16296_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing G-protein coupled receptor 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040311 GCST90234511 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Roundabout homolog 4 level in Chronic kidney disease with hypertension and no diabetes (16297_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of roundabout homolog 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043306 GCST90234512 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Group IID secretory phospholipase A2 level in Chronic kidney disease with hypertension and no diabetes (16298_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of group IID secretory phospholipase A2 in blood serum http://purl.obolibrary.org/obo/OBA_2042914 GCST90234513 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mediator of RNA polymerase II transcription subunit 1 level in Chronic kidney disease with hypertension and no diabetes (3892_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 mediator of RNA polymerase II transcription subunit 1 measurement http://www.ebi.ac.uk/efo/EFO_0008228 GCST90237540 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mesothelin level in Chronic kidney disease with hypertension and no diabetes (3893_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 mesothelin measurement http://www.ebi.ac.uk/efo/EFO_0020565 GCST90237541 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetyl-D-glucosamine kinase level in Chronic kidney disease with hypertension and no diabetes (3894_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 N-acetyl-D-glucosamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0008239 GCST90237542 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyridoxal phosphate phosphatase level in Chronic kidney disease with hypertension and no diabetes (3897_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 pyridoxal phosphate phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0020694 GCST90237543 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S proteasome non-ATPase regulatory subunit 7 level in Chronic kidney disease with hypertension and no diabetes (3898_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 26s proteasome non-atpase regulatory subunit 7 measurement http://www.ebi.ac.uk/efo/EFO_0020112 GCST90237544 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-phase kinase-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (3902_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 s-phase kinase-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020715 GCST90237545 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-4 level in Chronic kidney disease with hypertension and no diabetes (3903_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 sorting nexin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020747 GCST90237546 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 N level in Chronic kidney disease with hypertension and no diabetes (3905_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin-conjugating enzyme E2 N measurement http://www.ebi.ac.uk/efo/EFO_0020841 GCST90237547 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyridoxal kinase level in Chronic kidney disease with hypertension and no diabetes (11098_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 pyridoxal kinase measurement http://www.ebi.ac.uk/efo/EFO_0021919 GCST90233058 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 4 level in Chronic kidney disease with hypertension and no diabetes (11101_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 toll-like receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0021920 GCST90233059 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock protein beta-1 level in Chronic kidney disease with hypertension and no diabetes (11103_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0010595 GCST90233060 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chitinase-3-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (11104_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of chitinase-3-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041005 GCST90233061 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-enolase level in Chronic kidney disease with hypertension and no diabetes (11105_171) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021922 GCST90233062 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Teneurin-3 level in Chronic kidney disease with hypertension and no diabetes (11107_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of teneurin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042693 GCST90233063 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (11109_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233064 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 119 level in Chronic kidney disease with hypertension and no diabetes (11110_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 119 in blood serum http://purl.obolibrary.org/obo/OBA_2044408 GCST90233065 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kish-A level in Chronic kidney disease with hypertension and no diabetes (11112_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein kish-A in blood serum http://purl.obolibrary.org/obo/OBA_2044728 GCST90233066 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C11orf87 level in Chronic kidney disease with hypertension and no diabetes (11116_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C11orf87 in blood serum http://purl.obolibrary.org/obo/OBA_2044832 GCST90233067 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermatogenesis-associated protein 20 level in Chronic kidney disease with hypertension and no diabetes (11117_2) 466 African American individuals NA Illumina [14870897] (imputed) 3 level of spermatogenesis-associated protein 20 in blood serum http://purl.obolibrary.org/obo/OBA_2043617 GCST90233068 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-17 level in Chronic kidney disease with hypertension and no diabetes (11118_107) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Ras-related protein Rab-17 in blood serum http://purl.obolibrary.org/obo/OBA_2043141 GCST90233069 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetyltransferase 14 level in Chronic kidney disease with hypertension and no diabetes (11120_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable N-acetyltransferase 14 in blood serum http://purl.obolibrary.org/obo/OBA_2042516 GCST90233070 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brorin level in Chronic kidney disease with hypertension and no diabetes (11121_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of brorin in blood serum http://purl.obolibrary.org/obo/OBA_2044121 GCST90233071 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Maspardin level in Chronic kidney disease with hypertension and no diabetes (11122_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of maspardin in blood serum http://purl.obolibrary.org/obo/OBA_2043626 GCST90233072 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Triple functional domain protein level in Chronic kidney disease with hypertension and no diabetes (11126_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of triple functional domain protein in blood serum http://purl.obolibrary.org/obo/OBA_2043939 GCST90233073 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 132C level in Chronic kidney disease with hypertension and no diabetes (11128_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233074 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 15 level in Chronic kidney disease with hypertension and no diabetes (11129_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 15 in blood serum http://purl.obolibrary.org/obo/OBA_2040812 GCST90233075 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Voltage-dependent L-type calcium channel subunit beta-4 level in Chronic kidney disease with hypertension and no diabetes (11130_158) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-dependent L-type calcium channel subunit beta-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040870 GCST90233076 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptide chain release factor 1-like, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11134_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptide chain release factor 1-like, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042456 GCST90233077 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L55, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11135_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L55, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042433 GCST90233078 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine receptor common subunit beta level in Chronic kidney disease with hypertension and no diabetes (11137_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233079 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Runt-related transcription factor 3 level in Chronic kidney disease with hypertension and no diabetes (11138_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of runt-related transcription factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043356 GCST90233080 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(I) chain level in Chronic kidney disease with hypertension and no diabetes (11140_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233081 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (11142_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233082 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noelin-3 level in Chronic kidney disease with hypertension and no diabetes (11143_32) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233083 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 116 level in Chronic kidney disease with hypertension and no diabetes (11144_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 116 in blood serum http://purl.obolibrary.org/obo/OBA_2041275 GCST90233084 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0606 protein KIAA1549L level in Chronic kidney disease with hypertension and no diabetes (11145_72) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of UPF0606 protein KIAA1549L (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044909 GCST90233085 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-box transcription factor TBX22 level in Chronic kidney disease with hypertension and no diabetes (11146_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-box transcription factor TBX22 in blood serum http://purl.obolibrary.org/obo/OBA_2043796 GCST90233086 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trem-like transcript 1 protein level in Chronic kidney disease with hypertension and no diabetes (11147_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233087 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 1 level in Chronic kidney disease with hypertension and no diabetes (11149_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233088 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(VI) chain level in Chronic kidney disease with hypertension and no diabetes (11150_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 collagen alpha-1(VIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020269 GCST90233089 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-13 level in Chronic kidney disease with hypertension and no diabetes (11152_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-13 measurement http://www.ebi.ac.uk/efo/EFO_0020512 GCST90233090 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear factor erythroid 2-related factor 1 level in Chronic kidney disease with hypertension and no diabetes (11154_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoplasmic reticulum membrane sensor NFE2L1 in blood serum http://purl.obolibrary.org/obo/OBA_2042570 GCST90233091 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-5(VI) chain level in Chronic kidney disease with hypertension and no diabetes (11155_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-5(VI) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041086 GCST90233092 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (11157_35) 466 African American individuals NA Illumina [14870897] (imputed) 1 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90233093 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bicaudal D-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (11158_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BICD family-like cargo adapter 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044691 GCST90233094 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial ubiquitin ligase activator of NFKB 1 level in Chronic kidney disease with hypertension and no diabetes (11159_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233095 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 122 level in Chronic kidney disease with hypertension and no diabetes (11160_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RING finger protein 122 in blood serum http://purl.obolibrary.org/obo/OBA_2043289 GCST90233096 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spartin level in Chronic kidney disease with hypertension and no diabetes (11161_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spartin in blood serum http://purl.obolibrary.org/obo/OBA_2043625 GCST90233097 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Equatorin level in Chronic kidney disease with hypertension and no diabetes (11162_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of equatorin in blood serum http://purl.obolibrary.org/obo/OBA_2040529 GCST90233098 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM162B level in Chronic kidney disease with hypertension and no diabetes (11163_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM162B in blood serum http://purl.obolibrary.org/obo/OBA_2044441 GCST90233099 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase A level in Chronic kidney disease with hypertension and no diabetes (3844_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptidyl-prolyl cis-trans isomerase A measurement http://www.ebi.ac.uk/efo/EFO_0020625 GCST90237515 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynein light chain roadblock-type 1 level in Chronic kidney disease with hypertension and no diabetes (3845_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 dynein light chain roadblock-type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008114 GCST90237516 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Persulfide dioxygenase ETHE1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (3847_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 persulfide dioxygenase ETHE1, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0008258 GCST90237517 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 1 level in Chronic kidney disease with hypertension and no diabetes (3852_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 DNAj homolog subfamily b member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020332 GCST90237518 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Malate dehydrogenase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (3853_56) 466 African American individuals NA Illumina [14870897] (imputed) 1 malate dehydrogenase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020551 GCST90237519 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nascent polypeptide-associated complex subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3854_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 nascent polypeptide-associated complex subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020587 GCST90237520 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxiredoxin-1 level in Chronic kidney disease with hypertension and no diabetes (3855_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 peroxiredoxin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020629 GCST90237521 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low molecular weight phosphotyrosine protein phosphatase level in Chronic kidney disease with hypertension and no diabetes (3858_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 low molecular weight phosphotyrosine protein phosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008213 GCST90237522 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-1 level in Chronic kidney disease with hypertension and no diabetes (3859_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 proteasome subunit alpha type-1 measurement http://www.ebi.ac.uk/efo/EFO_0020663 GCST90237523 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-6 level in Chronic kidney disease with hypertension and no diabetes (3860_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 proteasome subunit alpha type-6 measurement http://www.ebi.ac.uk/efo/EFO_0020665 GCST90237524 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S7 level in Chronic kidney disease with hypertension and no diabetes (3864_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 40s ribosomal protein S7 measurement http://www.ebi.ac.uk/efo/EFO_0020118 GCST90237525 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosome maturation protein SBDS level in Chronic kidney disease with hypertension and no diabetes (3866_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 ribosome maturation protein sbds measurement http://www.ebi.ac.uk/efo/EFO_0020711 GCST90237526 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Seizure 6-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (3867_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 seizure 6-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020720 GCST90237527 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small glutamine-rich tetratricopeptide repeat-containing protein alpha level in Chronic kidney disease with hypertension and no diabetes (3868_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 small glutamine-rich tetratricopeptide repeat-containing protein alpha measurement http://www.ebi.ac.uk/efo/EFO_0020744 GCST90237528 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translationally-controlled tumor protein level in Chronic kidney disease with hypertension and no diabetes (3872_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 translationally-controlled tumor protein measurement http://www.ebi.ac.uk/efo/EFO_0020784 GCST90237529 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyroid peroxidase level in Chronic kidney disease with hypertension and no diabetes (3873_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 thyroid peroxidase measurement http://www.ebi.ac.uk/efo/EFO_0020775 GCST90237530 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 L3 level in Chronic kidney disease with hypertension and no diabetes (3874_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin-conjugating enzyme E2 L3 measurement http://www.ebi.ac.uk/efo/EFO_0020840 GCST90237531 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AT-rich interactive domain-containing protein 3A level in Chronic kidney disease with hypertension and no diabetes (3875_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 AT-rich interactive domain-containing protein 3A measurement http://www.ebi.ac.uk/efo/EFO_0020165 GCST90237532 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hsp90 co-chaperone Cdc37 level in Chronic kidney disease with hypertension and no diabetes (3879_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 hsp90 co-chaperone CDC37 measurement http://www.ebi.ac.uk/efo/EFO_0020458 GCST90237533 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynein light chain 1, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (3881_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 dynein light chain 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020339 GCST90237534 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Importin subunit beta-1 level in Chronic kidney disease with hypertension and no diabetes (3887_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 importin subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020468 GCST90237535 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibitor of growth protein 1 level in Chronic kidney disease with hypertension and no diabetes (3888_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 inhibitor of growth protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020471 GCST90237536 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lamin-B1 level in Chronic kidney disease with hypertension and no diabetes (3889_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 lamin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020527 GCST90237537 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. L-lactate dehydrogenase B chain level in Chronic kidney disease with hypertension and no diabetes (3890_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 L-lactate dehydrogenase B chain measurement http://www.ebi.ac.uk/efo/EFO_0020524 GCST90237538 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methyl-CpG-binding domain protein 4 level in Chronic kidney disease with hypertension and no diabetes (3891_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 methyl-cpg-binding domain protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020569 GCST90237539 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 9 level in Chronic kidney disease with hypertension and no diabetes (3798_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020232 GCST90237490 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 3 level in Chronic kidney disease with hypertension and no diabetes (3799_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020229 GCST90237491 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Creatine kinase B-type level in Chronic kidney disease with hypertension and no diabetes (3800_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 creatine kinase b-type measurement http://www.ebi.ac.uk/efo/EFO_0020290 GCST90237492 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-D level in Chronic kidney disease with hypertension and no diabetes (3803_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90237493 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelial cell-specific molecule 1 level in Chronic kidney disease with hypertension and no diabetes (3805_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 endothelial cell-specific molecule 1 measurement http://www.ebi.ac.uk/efo/EFO_0010912 GCST90237494 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 5 level in Chronic kidney disease with hypertension and no diabetes (3806_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-a receptor 5 measurement http://www.ebi.ac.uk/efo/EFO_0020353 GCST90237495 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 23 level in Chronic kidney disease with hypertension and no diabetes (3807_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 23 measurement http://www.ebi.ac.uk/efo/EFO_0009381 GCST90237496 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor receptor 2 level in Chronic kidney disease with hypertension and no diabetes (3808_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020389 GCST90237497 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor receptor 3 level in Chronic kidney disease with hypertension and no diabetes (3809_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90237498 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase Fyn level in Chronic kidney disease with hypertension and no diabetes (3813_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase FYN measurement http://www.ebi.ac.uk/efo/EFO_0020823 GCST90237499 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-11 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3814_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-11 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020491 GCST90237500 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-12 receptor subunit beta-2 level in Chronic kidney disease with hypertension and no diabetes (3815_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-12 receptor subunit beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020492 GCST90237501 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C theta type level in Chronic kidney disease with hypertension and no diabetes (3817_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein kinase c theta type measurement http://www.ebi.ac.uk/efo/EFO_0020682 GCST90237502 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAP kinase-activated protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (3820_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 MAP kinase-activated protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008225 GCST90237503 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAP kinase-activated protein kinase 5 level in Chronic kidney disease with hypertension and no diabetes (3821_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 MAP kinase-activated protein kinase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020553 GCST90237504 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAP kinase-activated protein kinase 3 level in Chronic kidney disease with hypertension and no diabetes (3822_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 MAP kinase-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0008226 GCST90237505 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Megakaryocyte-associated tyrosine-protein kinase level in Chronic kidney disease with hypertension and no diabetes (3823_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 megakaryocyte-associated tyrosine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0020562 GCST90237506 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 8 level in Chronic kidney disease with hypertension and no diabetes (3825_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020580 GCST90237507 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase PAK 6 level in Chronic kidney disease with hypertension and no diabetes (3827_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase PAK 6 measurement http://www.ebi.ac.uk/efo/EFO_0020729 GCST90237508 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor C level in Chronic kidney disease with hypertension and no diabetes (3828_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet-derived growth factor c measurement http://www.ebi.ac.uk/efo/EFO_0020648 GCST90237509 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase PTEN level in Chronic kidney disease with hypertension and no diabetes (3831_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase and dual-specificity protein phosphatase pten measurement http://www.ebi.ac.uk/efo/EFO_0020635 GCST90237510 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-tyrosine kinase 6 level in Chronic kidney disease with hypertension and no diabetes (3832_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein-tyrosine kinase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020691 GCST90237511 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 2 level in Chronic kidney disease with hypertension and no diabetes (3835_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 toll-like receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020777 GCST90237512 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-fold modifier 1 level in Chronic kidney disease with hypertension and no diabetes (3836_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin-fold modifier 1 measurement http://www.ebi.ac.uk/efo/EFO_0020842 GCST90237513 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AH receptor-interacting protein level in Chronic kidney disease with hypertension and no diabetes (3839_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 AH receptor-interacting protein measurement http://www.ebi.ac.uk/efo/EFO_0020134 GCST90237514 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-associated domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (25480_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-associated domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043985 GCST90236950 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ataxin-10 level in Chronic kidney disease with hypertension and no diabetes (25481_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ataxin-10 in blood serum http://purl.obolibrary.org/obo/OBA_2040737 GCST90236951 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear factor 1 A-type level in Chronic kidney disease with hypertension and no diabetes (25482_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear factor 1 A-type in blood serum http://purl.obolibrary.org/obo/OBA_2042572 GCST90236952 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AT-rich interactive domain-containing protein 3C level in Chronic kidney disease with hypertension and no diabetes (25484_120) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AT-rich interactive domain-containing protein 3C in blood serum http://purl.obolibrary.org/obo/OBA_2044535 GCST90236953 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L38, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (25486_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L38, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042431 GCST90236954 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family O member 2 level in Chronic kidney disease with hypertension and no diabetes (25488_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family O member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044344 GCST90236955 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum junction formation protein lunapark level in Chronic kidney disease with hypertension and no diabetes (25491_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoplasmic reticulum junction formation protein lunapark in blood serum http://purl.obolibrary.org/obo/OBA_2042215 GCST90236956 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Target of Myb protein 1 level in Chronic kidney disease with hypertension and no diabetes (25492_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of target of Myb1 membrane trafficking protein in blood serum http://purl.obolibrary.org/obo/OBA_2043898 GCST90236957 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM221B level in Chronic kidney disease with hypertension and no diabetes (25493_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein FAM221B in blood serum http://purl.obolibrary.org/obo/OBA_2044697 GCST90236958 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SEC14-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (25497_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SEC14-like protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043418 GCST90236959 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipase DDHD2 level in Chronic kidney disease with hypertension and no diabetes (25499_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipase DDHD2 in blood serum http://purl.obolibrary.org/obo/OBA_2041252 GCST90236960 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab11 family-interacting protein 3 level in Chronic kidney disease with hypertension and no diabetes (25500_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab11 family-interacting protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044428 GCST90236961 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine-dependent hematopoietic cell linker level in Chronic kidney disease with hypertension and no diabetes (25501_128) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytokine-dependent hematopoietic cell linker in blood serum http://purl.obolibrary.org/obo/OBA_2041054 GCST90236962 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-endorphin level in Chronic kidney disease with hypertension and no diabetes (2558_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 beta-endorphin measurement http://www.ebi.ac.uk/efo/EFO_0008034 GCST90236963 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor I level in Chronic kidney disease with hypertension and no diabetes (2567_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement factor I measurement http://www.ebi.ac.uk/efo/EFO_0008099 GCST90236964 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dermokine level in Chronic kidney disease with hypertension and no diabetes (5963_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of dermokine in blood serum http://purl.obolibrary.org/obo/OBA_2041322 GCST90238130 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte cell-derived chemotaxin-2 level in Chronic kidney disease with hypertension and no diabetes (5970_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte cell-derived chemotaxin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042187 GCST90238131 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BolA-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (5980_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BolA-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040818 GCST90238132 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ES1 protein homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (5981_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamine amidotransferase-like class 1 domain-containing protein 3, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041222 GCST90238133 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (5982_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement factor H-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600054 GCST90238134 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 14 level in Chronic kidney disease with hypertension and no diabetes (5988_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90238135 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD8 alpha chain level in Chronic kidney disease with hypertension and no diabetes (5992_50) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of T-cell surface glycoprotein CD8 alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040238 GCST90238136 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialidase-1 level in Chronic kidney disease with hypertension and no diabetes (6003_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sialidase-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042564 GCST90238137 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q and tumor necrosis factor-related protein 9A level in Chronic kidney disease with hypertension and no diabetes (6019_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q and tumor necrosis factor-related protein 9A in blood serum http://purl.obolibrary.org/obo/OBA_2040853 GCST90238138 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urotensin-2 level in Chronic kidney disease with hypertension and no diabetes (6020_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of urotensin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2044071 GCST90238139 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stress-70 protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (13492_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stress-70 protein, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041949 GCST90233905 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate receptor ionotropic, delta-1 level in Chronic kidney disease with hypertension and no diabetes (13493_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamate receptor ionotropic, delta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041789 GCST90233906 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ceramide synthase 5 level in Chronic kidney disease with hypertension and no diabetes (13494_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ceramide synthase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042166 GCST90233907 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxycarboxylic acid receptor 2 level in Chronic kidney disease with hypertension and no diabetes (13495_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hydroxycarboxylic acid receptor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040314 GCST90233908 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxymethylglutaryl-CoA synthase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (13496_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hydroxymethylglutaryl-CoA synthase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2041892 GCST90233909 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 3 subunit J level in Chronic kidney disease with hypertension and no diabetes (13497_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 3 subunit J in blood serum http://purl.obolibrary.org/obo/OBA_2041448 GCST90233910 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol oxygenase level in Chronic kidney disease with hypertension and no diabetes (13498_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol oxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2042370 GCST90233911 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation Factor VIII level in Chronic kidney disease with hypertension and no diabetes (13499_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of coagulation factor VIII in blood serum http://purl.obolibrary.org/obo/OBA_2041536 GCST90233912 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Solute carrier family 35 member G2 level in Chronic kidney disease with hypertension and no diabetes (13501_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of solute carrier family 35 member G2 in blood serum http://purl.obolibrary.org/obo/OBA_2044355 GCST90233913 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium-independent sulfate anion transporter level in Chronic kidney disease with hypertension and no diabetes (13502_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium-independent sulfate anion transporter in blood serum http://purl.obolibrary.org/obo/OBA_2043529 GCST90233914 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PRA1 family protein 3 level in Chronic kidney disease with hypertension and no diabetes (13503_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PRA1 family protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040674 GCST90233915 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein R level in Chronic kidney disease with hypertension and no diabetes (13504_147) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein R in blood serum http://purl.obolibrary.org/obo/OBA_2041909 GCST90233916 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretory carrier-associated membrane protein 5 level in Chronic kidney disease with hypertension and no diabetes (13509_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretory carrier-associated membrane protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043390 GCST90233917 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sarcoplasmic/endoplasmic reticulum calcium ATPase 3 level in Chronic kidney disease with hypertension and no diabetes (13510_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sarcoplasmic/endoplasmic reticulum calcium ATPase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040728 GCST90233918 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-binding protein SATB1 level in Chronic kidney disease with hypertension and no diabetes (13511_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-binding protein SATB1 in blood serum http://purl.obolibrary.org/obo/OBA_2043387 GCST90233919 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein R level in Chronic kidney disease with hypertension and no diabetes (13512_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein R in blood serum http://purl.obolibrary.org/obo/OBA_2041909 GCST90233920 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 SUMO-protein ligase PIAS3 level in Chronic kidney disease with hypertension and no diabetes (13513_174) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 SUMO-protein ligase PIAS3 in blood serum http://purl.obolibrary.org/obo/OBA_2040445 GCST90233921 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulation of nuclear pre-mRNA domain-containing protein 1A level in Chronic kidney disease with hypertension and no diabetes (13515_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulation of nuclear pre-mRNA domain-containing protein 1A in blood serum http://purl.obolibrary.org/obo/OBA_2043329 GCST90233922 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ER membrane protein complex subunit 4 level in Chronic kidney disease with hypertension and no diabetes (13516_46) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ER membrane protein complex subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044291 GCST90233923 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Patched domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (13517_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of patched domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043086 GCST90233924 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (13518_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040689 GCST90233925 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho guanine nucleotide exchange factor 25 level in Chronic kidney disease with hypertension and no diabetes (13519_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho guanine nucleotide exchange factor 25 in blood serum http://purl.obolibrary.org/obo/OBA_2041700 GCST90233926 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Visinin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (13522_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of visinin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044116 GCST90233927 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan-sulfate 6-O-sulfotransferase 2 level in Chronic kidney disease with hypertension and no diabetes (13524_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heparan-sulfate 6-O-sulfotransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041935 GCST90233928 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Potassium voltage-gated channel subfamily G member 4 level in Chronic kidney disease with hypertension and no diabetes (13525_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-gated potassium channel subfamily G member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040223 GCST90233929 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nephronectin level in Chronic kidney disease with hypertension and no diabetes (6342_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of nephronectin in blood serum http://purl.obolibrary.org/obo/OBA_2042618 GCST90238215 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein C-II level in Chronic kidney disease with hypertension and no diabetes (6350_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apolipoprotein C-II in blood serum http://purl.obolibrary.org/obo/OBA_2040625 GCST90238216 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell antigen receptor complex-associated protein beta chain level in Chronic kidney disease with hypertension and no diabetes (6351_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell antigen receptor complex-associated protein beta chain in blood serum http://purl.obolibrary.org/obo/OBA_2040258 GCST90238217 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin receptor-related protein level in Chronic kidney disease with hypertension and no diabetes (6352_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin receptor-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2042038 GCST90238218 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hephaestin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (6354_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ferroxidase HEPHL1 in blood serum http://purl.obolibrary.org/obo/OBA_2041858 GCST90238219 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase B level in Chronic kidney disease with hypertension and no diabetes (6356_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase B in blood serum http://purl.obolibrary.org/obo/OBA_2041115 GCST90238220 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymotrypsin-like elastase family member 3B level in Chronic kidney disease with hypertension and no diabetes (6357_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chymotrypsin-like elastase family member 3B in blood serum http://purl.obolibrary.org/obo/OBA_2041461 GCST90238221 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (6359_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein O-linked-mannose beta-1,4-N-acetylglucosaminyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044560 GCST90238222 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 128 level in Chronic kidney disease with hypertension and no diabetes (6360_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 128 in blood serum http://purl.obolibrary.org/obo/OBA_2041281 GCST90238223 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-type tyrosine-protein phosphatase R level in Chronic kidney disease with hypertension and no diabetes (6361_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of receptor-type tyrosine-protein phosphatase R in blood serum http://purl.obolibrary.org/obo/OBA_2043108 GCST90238224 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Augurin level in Chronic kidney disease with hypertension and no diabetes (6362_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of augurin in blood serum http://purl.obolibrary.org/obo/OBA_2044870 GCST90238225 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tapasin-related protein level in Chronic kidney disease with hypertension and no diabetes (6364_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tapasin-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2043776 GCST90238226 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol-trisphosphate 3-kinase A level in Chronic kidney disease with hypertension and no diabetes (13473_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol-trisphosphate 3-kinase A in blood serum http://purl.obolibrary.org/obo/OBA_2042062 GCST90233892 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase kappa 1 level in Chronic kidney disease with hypertension and no diabetes (13474_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase kappa 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041805 GCST90233893 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA/RNA-binding protein KIN17 level in Chronic kidney disease with hypertension and no diabetes (13476_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA/RNA-binding protein KIN17 in blood serum http://purl.obolibrary.org/obo/OBA_2042102 GCST90233894 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukotriene B4 receptor 1 level in Chronic kidney disease with hypertension and no diabetes (13477_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukotriene B4 receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040312 GCST90233895 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM171A2 level in Chronic kidney disease with hypertension and no diabetes (13479_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein FAM171A2 in blood serum http://purl.obolibrary.org/obo/OBA_2044667 GCST90233896 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein 2 level in Chronic kidney disease with hypertension and no diabetes (13481_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043802 GCST90233897 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CCR4-NOT transcription complex subunit 1 level in Chronic kidney disease with hypertension and no diabetes (13482_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CCR4-NOT transcription complex subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041068 GCST90233898 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(I) chain level in Chronic kidney disease with hypertension and no diabetes (13484_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233899 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 87B level in Chronic kidney disease with hypertension and no diabetes (13485_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transmembrane protein 87B in blood serum http://purl.obolibrary.org/obo/OBA_2044370 GCST90233900 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein unc-93 homolog B1 level in Chronic kidney disease with hypertension and no diabetes (13487_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein unc-93 homolog B1 in blood serum http://purl.obolibrary.org/obo/OBA_2044039 GCST90233901 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arfaptin-1 level in Chronic kidney disease with hypertension and no diabetes (13488_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arfaptin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040646 GCST90233902 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAGUK p55 subfamily member 6 level in Chronic kidney disease with hypertension and no diabetes (13490_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein PALS2 in blood serum http://purl.obolibrary.org/obo/OBA_2044332 GCST90233903 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta level in Chronic kidney disease with hypertension and no diabetes (13491_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit delta in blood serum http://purl.obolibrary.org/obo/OBA_2042822 GCST90233904 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. General transcription factor II-I level in Chronic kidney disease with hypertension and no diabetes (13609_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of general transcription factor II-I in blood serum http://purl.obolibrary.org/obo/OBA_2041816 GCST90233980 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 10 level in Chronic kidney disease with hypertension and no diabetes (13610_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042264 GCST90233981 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytohesin-interacting protein level in Chronic kidney disease with hypertension and no diabetes (13612_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytohesin-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2041221 GCST90233982 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CREB-binding protein level in Chronic kidney disease with hypertension and no diabetes (13614_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of CREB-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2040192 GCST90233983 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoplasmic protein NCK2 level in Chronic kidney disease with hypertension and no diabetes (13615_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytoplasmic protein NCK2 in blood serum http://purl.obolibrary.org/obo/OBA_2042527 GCST90233984 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitotic spindle assembly checkpoint protein MAD1 level in Chronic kidney disease with hypertension and no diabetes (13618_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitotic spindle assembly checkpoint protein MAD1 in blood serum http://purl.obolibrary.org/obo/OBA_2042257 GCST90233985 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATPase ASNA1 level in Chronic kidney disease with hypertension and no diabetes (13620_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATPase GET3 in blood serum http://purl.obolibrary.org/obo/OBA_2040703 GCST90233986 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-2 complex subunit alpha-2 level in Chronic kidney disease with hypertension and no diabetes (13621_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-2 complex subunit alpha-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040611 GCST90233987 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin polymerization-promoting protein family member 3 level in Chronic kidney disease with hypertension and no diabetes (20444_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin polymerization-promoting protein family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044453 GCST90235425 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-1 complex-associated regulatory protein level in Chronic kidney disease with hypertension and no diabetes (20445_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-1 complex-associated regulatory protein in blood serum http://purl.obolibrary.org/obo/OBA_2044645 GCST90235426 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein TGIF2LY level in Chronic kidney disease with hypertension and no diabetes (20447_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein TGIF2LY in blood serum http://purl.obolibrary.org/obo/OBA_2043837 GCST90235427 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerases I, II, and III subunit RPABC2 level in Chronic kidney disease with hypertension and no diabetes (20448_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerases I, II, and III subunit RPABC2 in blood serum http://purl.obolibrary.org/obo/OBA_2042969 GCST90235428 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Josephin-1 level in Chronic kidney disease with hypertension and no diabetes (20449_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of josephin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042073 GCST90235429 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intraflagellar transport protein 22 homolog level in Chronic kidney disease with hypertension and no diabetes (20451_126) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of intraflagellar transport protein 22 in blood serum http://purl.obolibrary.org/obo/OBA_2043177 GCST90235430 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Non-structural maintenance of chromosomes element 1 homolog level in Chronic kidney disease with hypertension and no diabetes (20453_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of non-structural maintenance of chromosomes element 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042646 GCST90235431 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SOSS complex subunit B2 level in Chronic kidney disease with hypertension and no diabetes (20454_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SOSS complex subunit B2 in blood serum http://purl.obolibrary.org/obo/OBA_2042687 GCST90235432 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase assembly factor 4 homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (20457_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil-helix-coiled-coil-helix domain-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044269 GCST90235433 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (20458_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042540 GCST90235434 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intraflagellar transport protein 20 homolog level in Chronic kidney disease with hypertension and no diabetes (20460_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of intraflagellar transport protein 20 in blood serum http://purl.obolibrary.org/obo/OBA_2041987 GCST90235435 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM50A level in Chronic kidney disease with hypertension and no diabetes (20461_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM50A in blood serum http://purl.obolibrary.org/obo/OBA_2044297 GCST90235436 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein IMPACT level in Chronic kidney disease with hypertension and no diabetes (20463_315) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein IMPACT in blood serum http://purl.obolibrary.org/obo/OBA_2042023 GCST90235437 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative KHDC1-like protein level in Chronic kidney disease with hypertension and no diabetes (20464_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235438 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctional adhesion molecule A level in Chronic kidney disease with hypertension and no diabetes (20511_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of junctional adhesion molecule A in blood serum http://purl.obolibrary.org/obo/OBA_2040343 GCST90235439 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen MUC18 level in Chronic kidney disease with hypertension and no diabetes (20512_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell surface glycoprotein MUC18 in blood serum http://purl.obolibrary.org/obo/OBA_2040245 GCST90235440 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BMP and activin membrane-bound inhibitor homolog level in Chronic kidney disease with hypertension and no diabetes (20514_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235441 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydropyrimidinase-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (13567_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydropyrimidinase-related protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041357 GCST90233955 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S proteasome non-ATPase regulatory subunit 4 level in Chronic kidney disease with hypertension and no diabetes (13568_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 26S proteasome non-ATPase regulatory subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040396 GCST90233956 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vigilin level in Chronic kidney disease with hypertension and no diabetes (13570_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vigilin in blood serum http://purl.obolibrary.org/obo/OBA_2041852 GCST90233957 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S proteasome non-ATPase regulatory subunit 11 level in Chronic kidney disease with hypertension and no diabetes (13572_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 26S proteasome non-ATPase regulatory subunit 11 in blood serum http://purl.obolibrary.org/obo/OBA_2040395 GCST90233958 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Actin-related protein 2/3 complex subunit 3 level in Chronic kidney disease with hypertension and no diabetes (13573_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin-related protein 2/3 complex subunit 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040682 GCST90233959 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-related GTP-binding protein Rho6 level in Chronic kidney disease with hypertension and no diabetes (13574_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-related GTP-binding protein Rho6 in blood serum http://purl.obolibrary.org/obo/OBA_2043286 GCST90233960 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Segment polarity protein dishevelled homolog DVL-2 level in Chronic kidney disease with hypertension and no diabetes (13575_40) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of segment polarity protein dishevelled homolog DVL-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041391 GCST90233961 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase P level in Chronic kidney disease with hypertension and no diabetes (13576_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90233962 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Splicing factor U2AF 65 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (13577_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of splicing factor U2AF 65 kDa subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043978 GCST90233963 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Actin-binding LIM protein 3 level in Chronic kidney disease with hypertension and no diabetes (13578_98) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin-binding LIM protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040462 GCST90233964 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-N-acetylhexosamine pyrophosphorylase level in Chronic kidney disease with hypertension and no diabetes (13580_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UDP-N-acetylhexosamine pyrophosphorylase in blood serum http://purl.obolibrary.org/obo/OBA_2043979 GCST90233965 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apoptotic protease-activating factor 1 level in Chronic kidney disease with hypertension and no diabetes (13583_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apoptotic protease-activating factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040401 GCST90233966 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A9 level in Chronic kidney disease with hypertension and no diabetes (13588_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A9 in blood serum http://purl.obolibrary.org/obo/OBA_2040604 GCST90233967 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 precursor protein-binding family B member 3 level in Chronic kidney disease with hypertension and no diabetes (13589_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233968 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oligoribonuclease, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (13590_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oligoribonuclease, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043244 GCST90233969 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA primase small subunit level in Chronic kidney disease with hypertension and no diabetes (13591_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA primase small subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043025 GCST90233970 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-binding protein GGA1 level in Chronic kidney disease with hypertension and no diabetes (13594_158) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-binding protein GGA1 in blood serum http://purl.obolibrary.org/obo/OBA_2041707 GCST90233971 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thiamine-triphosphatase level in Chronic kidney disease with hypertension and no diabetes (13595_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thiamine-triphosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2043845 GCST90233972 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-27B level in Chronic kidney disease with hypertension and no diabetes (13596_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-27B in blood serum http://purl.obolibrary.org/obo/OBA_2043150 GCST90233973 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-31 level in Chronic kidney disease with hypertension and no diabetes (13597_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-31 in blood serum http://purl.obolibrary.org/obo/OBA_2043153 GCST90233974 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab9 effector protein with kelch motifs level in Chronic kidney disease with hypertension and no diabetes (13599_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab9 effector protein with Kelch motifs in blood serum http://purl.obolibrary.org/obo/OBA_2043174 GCST90233975 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NHP2-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (13602_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NHP2-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042580 GCST90233976 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rieske domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (13603_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of rieske domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2044672 GCST90233977 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase NEURL1 level in Chronic kidney disease with hypertension and no diabetes (13604_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase NEURL1 in blood serum http://purl.obolibrary.org/obo/OBA_2042565 GCST90233978 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A10 level in Chronic kidney disease with hypertension and no diabetes (13605_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A10 in blood serum http://purl.obolibrary.org/obo/OBA_2040597 GCST90233979 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C-binding protein NELL2 level in Chronic kidney disease with hypertension and no diabetes (6022_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein kinase C-binding protein NELL2 in blood serum http://purl.obolibrary.org/obo/OBA_2042558 GCST90238140 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase E level in Chronic kidney disease with hypertension and no diabetes (6024_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 carboxypeptidase e measurement http://www.ebi.ac.uk/efo/EFO_0020234 GCST90238141 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Relaxin-3 level in Chronic kidney disease with hypertension and no diabetes (6027_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 relaxin receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021950 GCST90238142 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-galactoside alpha-2,6-sialyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (6035_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-galactoside alpha-2,6-sialyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043673 GCST90238143 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 10 level in Chronic kidney disease with hypertension and no diabetes (6036_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-a receptor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020350 GCST90238144 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Corticotropin-releasing factor-binding protein level in Chronic kidney disease with hypertension and no diabetes (6039_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of corticotropin-releasing factor-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2041140 GCST90238145 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-type tyrosine-protein phosphatase S level in Chronic kidney disease with hypertension and no diabetes (6049_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-type tyrosine-protein phosphatase S in blood serum http://purl.obolibrary.org/obo/OBA_2043109 GCST90238146 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexophilin-3 level in Chronic kidney disease with hypertension and no diabetes (6054_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90238147 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha/beta receptor 1 level in Chronic kidney disease with hypertension and no diabetes (6055_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 interferon alpha/beta receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021850 GCST90238148 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolactin-inducible protein level in Chronic kidney disease with hypertension and no diabetes (6060_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prolactin-inducible protein in blood serum http://purl.obolibrary.org/obo/OBA_2042896 GCST90238149 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfatase-modifying factor 2 level in Chronic kidney disease with hypertension and no diabetes (6069_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inactive C-alpha-formylglycine-generating enzyme 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043733 GCST90238150 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-hexosaminidase subunit beta level in Chronic kidney disease with hypertension and no diabetes (6075_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-hexosaminidase subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2041865 GCST90238151 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenosine deaminase CECR1 level in Chronic kidney disease with hypertension and no diabetes (6077_63) 466 African American individuals NA Illumina [14870897] (imputed) 1 adenosine deaminase measurement http://www.ebi.ac.uk/efo/EFO_0010761 GCST90238152 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2-phosphoxylose phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (6079_59) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 2-phosphoxylose phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040484 GCST90238153 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Procollagen C-endopeptidase enhancer 2 level in Chronic kidney disease with hypertension and no diabetes (6081_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of procollagen C-endopeptidase enhancer 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042803 GCST90238154 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chordin-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (6086_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chordin-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041016 GCST90238155 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor receptor-like 1 level in Chronic kidney disease with hypertension and no diabetes (6104_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor receptor-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041578 GCST90238156 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymotrypsin-like elastase family member 1 level in Chronic kidney disease with hypertension and no diabetes (6107_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of chymotrypsin-like elastase family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041459 GCST90238157 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelin-3 level in Chronic kidney disease with hypertension and no diabetes (6113_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endothelin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041415 GCST90238158 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroendocrine convertase 2 level in Chronic kidney disease with hypertension and no diabetes (6117_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroendocrine convertase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042807 GCST90238159 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAM domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (6119_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MAM domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044663 GCST90238160 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cellular tumor antigen p53 level in Chronic kidney disease with hypertension and no diabetes (6123_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 cellular tumor antigen p53 measurement http://www.ebi.ac.uk/efo/EFO_0022006 GCST90238161 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity mitogen-activated protein kinase kinase 3 level in Chronic kidney disease with hypertension and no diabetes (6151_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 dual specificity mitogen-activated protein kinase kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0022005 GCST90238162 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cellular tumor antigen p53 R175H mutant level in Chronic kidney disease with hypertension and no diabetes (6168_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cellular tumor antigen p53 in blood serum http://purl.obolibrary.org/obo/OBA_2040413 GCST90238163 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PolyUbiquitin K63-linked level in Chronic kidney disease with hypertension and no diabetes (6172_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 polyUbiquitin K63-linked measurement http://www.ebi.ac.uk/efo/EFO_0022008 GCST90238164 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable carboxypeptidase X1 level in Chronic kidney disease with hypertension and no diabetes (6255_74) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of probable carboxypeptidase X1 in blood serum http://purl.obolibrary.org/obo/OBA_2044275 GCST90238190 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte antigen 6 complex locus protein G6c level in Chronic kidney disease with hypertension and no diabetes (6256_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lymphocyte antigen 6 complex locus protein G6c in blood serum http://purl.obolibrary.org/obo/OBA_2042248 GCST90238191 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell growth regulator with EF hand domain protein 1 level in Chronic kidney disease with hypertension and no diabetes (6257_56) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cell growth regulator with EF hand domain protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040997 GCST90238192 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin level in Chronic kidney disease with hypertension and no diabetes (6260_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90238193 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17 receptor B level in Chronic kidney disease with hypertension and no diabetes (6262_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-17 receptor B in blood serum http://purl.obolibrary.org/obo/OBA_2042002 GCST90238194 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein CYR61 level in Chronic kidney disease with hypertension and no diabetes (6264_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CCN family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041216 GCST90238195 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stathmin-4 level in Chronic kidney disease with hypertension and no diabetes (6267_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stathmin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043704 GCST90238196 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolyl 3-hydroxylase 1 level in Chronic kidney disease with hypertension and no diabetes (6273_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prolyl 3-hydroxylase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042188 GCST90238197 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WSC domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (6274_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WSC domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044456 GCST90238198 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Furin level in Chronic kidney disease with hypertension and no diabetes (6276_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238199 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin-8 level in Chronic kidney disease with hypertension and no diabetes (6280_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin-8 in blood serum http://purl.obolibrary.org/obo/OBA_2042783 GCST90238200 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (6281_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044410 GCST90238201 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mast cell-expressed membrane protein 1 level in Chronic kidney disease with hypertension and no diabetes (6283_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mast cell-expressed membrane protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042313 GCST90238202 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ALK and LTK ligand 2 level in Chronic kidney disease with hypertension and no diabetes (6284_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ALK and LTK ligand 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044787 GCST90238203 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Malectin level in Chronic kidney disease with hypertension and no diabetes (6285_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of malectin in blood serum http://purl.obolibrary.org/obo/OBA_2042376 GCST90238204 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 36 level in Chronic kidney disease with hypertension and no diabetes (6289_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 36 in blood serum http://purl.obolibrary.org/obo/OBA_2044674 GCST90238205 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urotensin-2B level in Chronic kidney disease with hypertension and no diabetes (6290_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of urotensin-2B in blood serum http://purl.obolibrary.org/obo/OBA_2044072 GCST90238206 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calsyntenin-3 level in Chronic kidney disease with hypertension and no diabetes (6291_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calsyntenin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041058 GCST90238207 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B melanoma antigen 2 level in Chronic kidney disease with hypertension and no diabetes (6294_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B melanoma antigen 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040770 GCST90238208 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oncoprotein-induced transcript 3 protein level in Chronic kidney disease with hypertension and no diabetes (6296_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oncoprotein-induced transcript 3 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042698 GCST90238209 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q tumor necrosis factor-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (6304_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q tumor necrosis factor-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040849 GCST90238210 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipase B-like 1 level in Chronic kidney disease with hypertension and no diabetes (6315_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipase B-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044631 GCST90238211 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin gamma-A10 level in Chronic kidney disease with hypertension and no diabetes (6321_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin gamma-A10 in blood serum http://purl.obolibrary.org/obo/OBA_2042793 GCST90238212 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 4 level in Chronic kidney disease with hypertension and no diabetes (6326_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040205 GCST90238213 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive gamma-glutamyltranspeptidase 2 level in Chronic kidney disease with hypertension and no diabetes (6334_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-glutamyltranspeptidase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041712 GCST90238214 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prosaposin level in Chronic kidney disease with hypertension and no diabetes (6207_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prosaposin in blood serum http://purl.obolibrary.org/obo/OBA_2044552 GCST90238165 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amiloride-sensitive amine oxidase [copper-containing] level in Chronic kidney disease with hypertension and no diabetes (6209_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of amiloride-sensitive amine oxidase [copper-containing] in blood serum http://purl.obolibrary.org/obo/OBA_2040464 GCST90238166 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-5 level in Chronic kidney disease with hypertension and no diabetes (6210_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-5 in blood serum http://purl.obolibrary.org/obo/OBA_2041980 GCST90238167 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-8 level in Chronic kidney disease with hypertension and no diabetes (6214_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-8 in blood serum http://purl.obolibrary.org/obo/OBA_2041982 GCST90238168 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfhydryl oxidase 1 level in Chronic kidney disease with hypertension and no diabetes (6217_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfhydryl oxidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043135 GCST90238169 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ domain-containing protein 11 level in Chronic kidney disease with hypertension and no diabetes (6219_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ domain-containing protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2044340 GCST90238170 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-dependent glucokinase level in Chronic kidney disease with hypertension and no diabetes (6221_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-dependent glucokinase in blood serum http://purl.obolibrary.org/obo/OBA_2040523 GCST90238171 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylate cyclase activator 2B level in Chronic kidney disease with hypertension and no diabetes (6223_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanylate cyclase activator 2B in blood serum http://purl.obolibrary.org/obo/OBA_2041822 GCST90238172 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostasin level in Chronic kidney disease with hypertension and no diabetes (6225_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostasin in blood serum http://purl.obolibrary.org/obo/OBA_2043048 GCST90238173 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium uptake protein 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (6226_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium uptake protein 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044287 GCST90238174 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-10 level in Chronic kidney disease with hypertension and no diabetes (6227_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kallikrein-10 in blood serum http://purl.obolibrary.org/obo/OBA_2042126 GCST90238175 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm acrosome membrane-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (6228_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm acrosome membrane-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043607 GCST90238176 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chorionic somatomammotropin hormone level in Chronic kidney disease with hypertension and no diabetes (6229_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 chorionic somatomammotropin hormone measurement http://www.ebi.ac.uk/efo/EFO_0021929 GCST90238177 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cerberus level in Chronic kidney disease with hypertension and no diabetes (6230_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cerberus in blood serum http://purl.obolibrary.org/obo/OBA_2040988 GCST90238178 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stanniocalcin-2 level in Chronic kidney disease with hypertension and no diabetes (6231_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stanniocalcin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043698 GCST90238179 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-lymphocyte activation antigen CD86 level in Chronic kidney disease with hypertension and no diabetes (6232_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 t-lymphocyte activation antigen CD86 measurement http://www.ebi.ac.uk/efo/EFO_0020762 GCST90238180 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitrin level in Chronic kidney disease with hypertension and no diabetes (6234_74) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of vitrin in blood serum http://purl.obolibrary.org/obo/OBA_2044102 GCST90238181 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen triple helix repeat-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (6236_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen triple helix repeat-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041185 GCST90238182 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor receptor-like 1 level in Chronic kidney disease with hypertension and no diabetes (6237_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor receptor-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041578 GCST90238183 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 8 level in Chronic kidney disease with hypertension and no diabetes (6238_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pregnancy-specific beta-1-glycoprotein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2043062 GCST90238184 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. R-spondin-1 level in Chronic kidney disease with hypertension and no diabetes (6240_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of R-spondin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043350 GCST90238185 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nectin-2 level in Chronic kidney disease with hypertension and no diabetes (6245_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nectin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040385 GCST90238186 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal-regulatory protein beta-1 level in Chronic kidney disease with hypertension and no diabetes (6247_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of signal-regulatory protein beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040389 GCST90238187 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 6 level in Chronic kidney disease with hypertension and no diabetes (6248_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90238188 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretoglobin family 3A member 1 level in Chronic kidney disease with hypertension and no diabetes (6252_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretoglobin family 3A member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043399 GCST90238189 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lupus La protein level in Chronic kidney disease with hypertension and no diabetes (13526_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233930 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleosome assembly protein 1-like 2 level in Chronic kidney disease with hypertension and no diabetes (13529_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleosome assembly protein 1-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042507 GCST90233931 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urotensin-2 receptor level in Chronic kidney disease with hypertension and no diabetes (13530_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of urotensin-2 receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040309 GCST90233932 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear envelope phosphatase-regulatory subunit 1 level in Chronic kidney disease with hypertension and no diabetes (13532_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear envelope phosphatase-regulatory subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044764 GCST90233933 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myomesin-2 level in Chronic kidney disease with hypertension and no diabetes (13534_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myomesin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042489 GCST90233934 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen type IV alpha-3-binding protein level in Chronic kidney disease with hypertension and no diabetes (13535_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233935 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA polymerase iota level in Chronic kidney disease with hypertension and no diabetes (13536_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA polymerase iota in blood serum http://purl.obolibrary.org/obo/OBA_2042964 GCST90233936 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small conductance calcium-activated potassium channel protein 1 level in Chronic kidney disease with hypertension and no diabetes (13539_131) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small conductance calcium-activated potassium channel protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040221 GCST90233937 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G-protein coupled receptor 26 level in Chronic kidney disease with hypertension and no diabetes (13540_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of G-protein coupled receptor 26 in blood serum http://purl.obolibrary.org/obo/OBA_2040315 GCST90233938 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myc target protein 1 level in Chronic kidney disease with hypertension and no diabetes (13541_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Myc target protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042478 GCST90233939 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin reductase 1 level in Chronic kidney disease with hypertension and no diabetes (13543_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostaglandin reductase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043092 GCST90233940 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 45 level in Chronic kidney disease with hypertension and no diabetes (13544_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 45 in blood serum http://purl.obolibrary.org/obo/OBA_2041894 GCST90233941 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable RNA-binding protein EIF1AD level in Chronic kidney disease with hypertension and no diabetes (13545_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable RNA-binding protein EIF1AD in blood serum http://purl.obolibrary.org/obo/OBA_2044290 GCST90233942 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5-hydroxytryptamine receptor 7 level in Chronic kidney disease with hypertension and no diabetes (13547_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5-hydroxytryptamine receptor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040243 GCST90233943 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidate phosphatase PPAPDC1A level in Chronic kidney disease with hypertension and no diabetes (13548_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipid phosphatase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044685 GCST90233944 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 29 level in Chronic kidney disease with hypertension and no diabetes (13549_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 29 in blood serum http://purl.obolibrary.org/obo/OBA_2040500 GCST90233945 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Switch-associated protein 70 level in Chronic kidney disease with hypertension and no diabetes (13552_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of switch-associated protein 70 in blood serum http://purl.obolibrary.org/obo/OBA_2043741 GCST90233946 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DCN1-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (13553_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DCN1-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041248 GCST90233947 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Replication initiator 1 level in Chronic kidney disease with hypertension and no diabetes (13554_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of replication initiator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043239 GCST90233948 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5-hydroxytryptamine receptor 2A level in Chronic kidney disease with hypertension and no diabetes (13556_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5-hydroxytryptamine receptor 2A in blood serum http://purl.obolibrary.org/obo/OBA_2040252 GCST90233949 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nectin-3 level in Chronic kidney disease with hypertension and no diabetes (13557_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nectin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040386 GCST90233950 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5-hydroxytryptamine receptor 6 level in Chronic kidney disease with hypertension and no diabetes (13561_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 5-hydroxytryptamine receptor 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040242 GCST90233951 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-CoA-binding domain-containing protein 7 level in Chronic kidney disease with hypertension and no diabetes (13563_259) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of acyl-CoA-binding domain-containing protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044758 GCST90233952 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoblastoma-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (13565_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of retinoblastoma-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040198 GCST90233953 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA polymerase II subunit A C-terminal domain phosphatase SSU72 level in Chronic kidney disease with hypertension and no diabetes (13566_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA polymerase II subunit A C-terminal domain phosphatase SSU72 in blood serum http://purl.obolibrary.org/obo/OBA_2043668 GCST90233954 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium channel subunit beta-3 level in Chronic kidney disease with hypertension and no diabetes (20516_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sodium channel subunit beta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043405 GCST90235442 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmoglein-2 level in Chronic kidney disease with hypertension and no diabetes (20517_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 desmoglein-2 measurement http://www.ebi.ac.uk/efo/EFO_0020322 GCST90235443 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD6 level in Chronic kidney disease with hypertension and no diabetes (20519_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD6 measurement http://www.ebi.ac.uk/efo/EFO_0010774 GCST90235444 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM3C level in Chronic kidney disease with hypertension and no diabetes (20520_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM3C in blood serum http://purl.obolibrary.org/obo/OBA_2044299 GCST90235445 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD28 level in Chronic kidney disease with hypertension and no diabetes (20521_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-cell-specific surface glycoprotein CD28 in blood serum http://purl.obolibrary.org/obo/OBA_2040336 GCST90235446 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor accessory protein-like 1 level in Chronic kidney disease with hypertension and no diabetes (20522_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-1 receptor accessory protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042009 GCST90235447 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pro-neuregulin-3, membrane-bound isoform level in Chronic kidney disease with hypertension and no diabetes (20524_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pro-neuregulin-3, membrane-bound isoform in blood serum http://purl.obolibrary.org/obo/OBA_2042638 GCST90235448 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase A4 level in Chronic kidney disease with hypertension and no diabetes (20525_200) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein disulfide-isomerase A4 in blood serum http://purl.obolibrary.org/obo/OBA_2042828 GCST90235449 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoic acid early transcript 1L protein level in Chronic kidney disease with hypertension and no diabetes (20526_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of UL16-binding protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043185 GCST90235450 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-5B level in Chronic kidney disease with hypertension and no diabetes (20527_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-5B in blood serum http://purl.obolibrary.org/obo/OBA_2043435 GCST90235451 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrosialin level in Chronic kidney disease with hypertension and no diabetes (20528_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of macrosialin in blood serum http://purl.obolibrary.org/obo/OBA_2040383 GCST90235452 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-10 level in Chronic kidney disease with hypertension and no diabetes (20529_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-10 in blood serum http://purl.obolibrary.org/obo/OBA_2040957 GCST90235453 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-6D level in Chronic kidney disease with hypertension and no diabetes (20530_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-6D in blood serum http://purl.obolibrary.org/obo/OBA_2043437 GCST90235454 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLAM family member 9 level in Chronic kidney disease with hypertension and no diabetes (20531_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of SLAM family member 9 in blood serum http://purl.obolibrary.org/obo/OBA_2043522 GCST90235455 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-35 level in Chronic kidney disease with hypertension and no diabetes (20533_39) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235456 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor class B member 1 level in Chronic kidney disease with hypertension and no diabetes (20534_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of scavenger receptor class B member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043393 GCST90235457 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17 receptor E level in Chronic kidney disease with hypertension and no diabetes (20535_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-17 receptor E in blood serum http://purl.obolibrary.org/obo/OBA_2042004 GCST90235458 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelial cell-selective adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (20536_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90235459 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 11 level in Chronic kidney disease with hypertension and no diabetes (20538_71) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235460 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil defensin 3 level in Chronic kidney disease with hypertension and no diabetes (20539_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neutrophil defensin 3 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044901 GCST90235461 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-4G level in Chronic kidney disease with hypertension and no diabetes (20540_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-4G in blood serum http://purl.obolibrary.org/obo/OBA_2043434 GCST90235462 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcitonin receptor level in Chronic kidney disease with hypertension and no diabetes (20542_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcitonin receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040878 GCST90235463 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 127 level in Chronic kidney disease with hypertension and no diabetes (20543_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 127 in blood serum http://purl.obolibrary.org/obo/OBA_2041280 GCST90235464 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate receptor ionotropic, kainate 2 level in Chronic kidney disease with hypertension and no diabetes (20544_103) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamate receptor ionotropic, kainate 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041791 GCST90235465 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microfibril-associated glycoprotein 3 level in Chronic kidney disease with hypertension and no diabetes (20545_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microfibril-associated glycoprotein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042350 GCST90235466 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 level in Chronic kidney disease with hypertension and no diabetes (21126_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamine--fructose-6-phosphate aminotransferase [isomerizing] 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041705 GCST90235577 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CDK2 level in Chronic kidney disease with hypertension and no diabetes (21128_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040965 GCST90235578 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAD2L1-binding protein level in Chronic kidney disease with hypertension and no diabetes (21129_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MAD2L1-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2042259 GCST90235579 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol-tetrakisphosphate 1-kinase level in Chronic kidney disease with hypertension and no diabetes (21130_82) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of inositol-tetrakisphosphate 1-kinase in blood serum http://purl.obolibrary.org/obo/OBA_2042061 GCST90235580 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA wybutosine-synthesizing protein 5 level in Chronic kidney disease with hypertension and no diabetes (21131_109) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA wybutosine-synthesizing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044797 GCST90235581 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-13 level in Chronic kidney disease with hypertension and no diabetes (21132_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-13 in blood serum http://purl.obolibrary.org/obo/OBA_2043751 GCST90235582 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cx9C motif-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (21133_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Cx9C motif-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044562 GCST90235583 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CREB/ATF bZIP transcription factor level in Chronic kidney disease with hypertension and no diabetes (21134_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CREB/ATF bZIP transcription factor in blood serum http://purl.obolibrary.org/obo/OBA_2041136 GCST90235584 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Splicing factor 3B subunit 6 level in Chronic kidney disease with hypertension and no diabetes (21135_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of splicing factor 3B subunit 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043473 GCST90235585 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome assembly chaperone 2 level in Chronic kidney disease with hypertension and no diabetes (21136_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome assembly chaperone 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043080 GCST90235586 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleoplasmin-2 level in Chronic kidney disease with hypertension and no diabetes (21138_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleoplasmin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042617 GCST90235587 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium signal-modulating cyclophilin ligand level in Chronic kidney disease with hypertension and no diabetes (21140_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guided entry of tail-anchored proteins factor CAMLG in blood serum http://purl.obolibrary.org/obo/OBA_2040884 GCST90235588 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM84B level in Chronic kidney disease with hypertension and no diabetes (21141_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein LRATD2 in blood serum http://purl.obolibrary.org/obo/OBA_2044298 GCST90235589 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcyphosin level in Chronic kidney disease with hypertension and no diabetes (21143_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcyphosin in blood serum http://purl.obolibrary.org/obo/OBA_2040894 GCST90235590 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase Sgk1 level in Chronic kidney disease with hypertension and no diabetes (21144_160) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase Sgk1 in blood serum http://purl.obolibrary.org/obo/OBA_2043483 GCST90235591 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubby-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (21146_187) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubby-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043961 GCST90235592 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fructosamine-3-kinase level in Chronic kidney disease with hypertension and no diabetes (21147_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of fructosamine-3-kinase in blood serum http://purl.obolibrary.org/obo/OBA_2041598 GCST90235593 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUE domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (21149_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CUE domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044756 GCST90235594 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eyes absent homolog 2 level in Chronic kidney disease with hypertension and no diabetes (21152_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eyes absent homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041530 GCST90235595 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromatin complexes subunit BAP18 level in Chronic kidney disease with hypertension and no diabetes (21153_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromatin complexes subunit BAP18 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044911 GCST90235596 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-binding protein 39-like level in Chronic kidney disease with hypertension and no diabetes (21154_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-binding protein 39-like in blood serum http://purl.obolibrary.org/obo/OBA_2040863 GCST90235597 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative glutathione-specific gamma-glutamylcyclotransferase 2 level in Chronic kidney disease with hypertension and no diabetes (21156_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione-specific gamma-glutamylcyclotransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040999 GCST90235598 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxylysine kinase level in Chronic kidney disease with hypertension and no diabetes (21157_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aminoglycoside phosphotransferase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044237 GCST90235599 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Charged multivesicular body protein 6 level in Chronic kidney disease with hypertension and no diabetes (21160_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of charged multivesicular body protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041013 GCST90235600 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. rRNA methyltransferase 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21161_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of rRNA methyltransferase 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044606 GCST90235601 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S14 level in Chronic kidney disease with hypertension and no diabetes (20964_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 40S ribosomal protein S14 in blood serum http://purl.obolibrary.org/obo/OBA_2043331 GCST90235527 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated proteins 1A/1B light chain 3 beta 2 level in Chronic kidney disease with hypertension and no diabetes (20965_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated proteins 1A/1B light chain 3 beta 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042284 GCST90235528 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sentrin-specific protease 8 level in Chronic kidney disease with hypertension and no diabetes (20966_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sentrin-specific protease 8 in blood serum http://purl.obolibrary.org/obo/OBA_2043442 GCST90235529 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome assembly chaperone 4 level in Chronic kidney disease with hypertension and no diabetes (20967_137) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome assembly chaperone 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043082 GCST90235530 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Exosome complex component RRP46 level in Chronic kidney disease with hypertension and no diabetes (20968_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of exosome complex component RRP46 in blood serum http://purl.obolibrary.org/obo/OBA_2041527 GCST90235531 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING1 and YY1-binding protein level in Chronic kidney disease with hypertension and no diabetes (20969_114) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RING1 and YY1-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2043360 GCST90235532 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dysbindin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (20970_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dysbindin domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044747 GCST90235533 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionine-R-sulfoxide reductase B1 level in Chronic kidney disease with hypertension and no diabetes (20971_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methionine-R-sulfoxide reductase B1 in blood serum http://purl.obolibrary.org/obo/OBA_2043453 GCST90235534 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cleavage and polyadenylation specificity factor subunit 5 level in Chronic kidney disease with hypertension and no diabetes (20972_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cleavage and polyadenylation specificity factor subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042670 GCST90235535 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcipressin-2 level in Chronic kidney disease with hypertension and no diabetes (20975_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcipressin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043217 GCST90235536 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U6 snRNA-associated Sm-like protein LSm3 level in Chronic kidney disease with hypertension and no diabetes (20976_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U6 snRNA-associated Sm-like protein LSm3 in blood serum http://purl.obolibrary.org/obo/OBA_2042242 GCST90235537 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosducin-like protein level in Chronic kidney disease with hypertension and no diabetes (20977_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosducin-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042816 GCST90235538 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription initiation factor IIB level in Chronic kidney disease with hypertension and no diabetes (20979_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription initiation factor IIB in blood serum http://purl.obolibrary.org/obo/OBA_2041813 GCST90235539 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U11/U12 small nuclear ribonucleoprotein 25 kDa protein level in Chronic kidney disease with hypertension and no diabetes (20982_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U11/U12 small nuclear ribonucleoprotein 25 kDa protein in blood serum http://purl.obolibrary.org/obo/OBA_2043571 GCST90235540 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 19 level in Chronic kidney disease with hypertension and no diabetes (20984_142) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 19 in blood serum http://purl.obolibrary.org/obo/OBA_2041383 GCST90235541 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Egl nine homolog 3 level in Chronic kidney disease with hypertension and no diabetes (20986_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prolyl hydroxylase EGLN3 in blood serum http://purl.obolibrary.org/obo/OBA_2041430 GCST90235542 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein SIX6 level in Chronic kidney disease with hypertension and no diabetes (20987_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of homeobox protein SIX6 in blood serum http://purl.obolibrary.org/obo/OBA_2043517 GCST90235543 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinitis pigmentosa 9 protein level in Chronic kidney disease with hypertension and no diabetes (20988_63) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of retinitis pigmentosa 9 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043313 GCST90235544 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyrotroph embryonic factor level in Chronic kidney disease with hypertension and no diabetes (20990_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thyrotroph embryonic factor in blood serum http://purl.obolibrary.org/obo/OBA_2043825 GCST90235545 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (20991_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LIM domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044714 GCST90235546 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BEN domain-containing protein 6 level in Chronic kidney disease with hypertension and no diabetes (20993_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BEN domain-containing protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2044719 GCST90235547 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family F member 2 level in Chronic kidney disease with hypertension and no diabetes (20994_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family F member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044343 GCST90235548 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerase II subunit RPB3 level in Chronic kidney disease with hypertension and no diabetes (20995_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerase II subunit RPB3 in blood serum http://purl.obolibrary.org/obo/OBA_2042967 GCST90235549 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Succinate dehydrogenase assembly factor 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (20996_107) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of succinate dehydrogenase assembly factor 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044473 GCST90235550 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nicotinamide riboside kinase 2; Short=NRK 2; Short=NmR-K 2; EC=2.7.1.22 level in Chronic kidney disease with hypertension and no diabetes (20998_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nicotinamide riboside kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042051 GCST90235551 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S ribosomal protein L5 level in Chronic kidney disease with hypertension and no diabetes (20999_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S ribosomal protein L5 in blood serum http://purl.obolibrary.org/obo/OBA_2043323 GCST90235552 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BRICK1 level in Chronic kidney disease with hypertension and no diabetes (21001_393) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BRICK1 in blood serum http://purl.obolibrary.org/obo/OBA_2044511 GCST90235553 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NudC domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (21002_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NudC domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044586 GCST90235554 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein mago nashi homolog level in Chronic kidney disease with hypertension and no diabetes (21008_113) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein mago nashi in blood serum http://purl.obolibrary.org/obo/OBA_2042272 GCST90235555 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sentan level in Chronic kidney disease with hypertension and no diabetes (21009_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sentan in blood serum http://purl.obolibrary.org/obo/OBA_2044782 GCST90235556 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein unc-119 homolog B level in Chronic kidney disease with hypertension and no diabetes (21105_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein unc-119 homolog B in blood serum http://purl.obolibrary.org/obo/OBA_2044033 GCST90235557 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centrin-1 level in Chronic kidney disease with hypertension and no diabetes (21106_206) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centrin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040990 GCST90235558 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complex I intermediate-associated protein 30, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21107_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complex I intermediate-associated protein 30, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044654 GCST90235559 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized metallophosphoesterase CSTP1 level in Chronic kidney disease with hypertension and no diabetes (21108_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine/threonine-protein phosphatase CPPED1 in blood serum http://purl.obolibrary.org/obo/OBA_2044274 GCST90235560 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cilia- and flagella-associated protein 36 level in Chronic kidney disease with hypertension and no diabetes (21109_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cilia- and flagella-associated protein 36 in blood serum http://purl.obolibrary.org/obo/OBA_2044257 GCST90235561 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 Z level in Chronic kidney disease with hypertension and no diabetes (21110_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 Z in blood serum http://purl.obolibrary.org/obo/OBA_2044006 GCST90235562 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hsp70-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (21111_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Hsp70-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041952 GCST90235563 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin regulatory light chain 2, skeletal muscle isoform level in Chronic kidney disease with hypertension and no diabetes (21112_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin regulatory light chain 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042485 GCST90235564 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TRAF-interacting protein with FHA domain-containing protein A level in Chronic kidney disease with hypertension and no diabetes (21113_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TRAF-interacting protein with FHA domain-containing protein A in blood serum http://purl.obolibrary.org/obo/OBA_2040429 GCST90235565 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 12 level in Chronic kidney disease with hypertension and no diabetes (21114_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 12 in blood serum http://purl.obolibrary.org/obo/OBA_2044281 GCST90235566 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-miRNA 5'-monophosphate methyltransferase level in Chronic kidney disease with hypertension and no diabetes (21115_48) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of methyltransferase BCDIN3D in blood serum http://purl.obolibrary.org/obo/OBA_2044601 GCST90235567 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polycomb protein EED level in Chronic kidney disease with hypertension and no diabetes (21116_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polycomb protein EED in blood serum http://purl.obolibrary.org/obo/OBA_2041417 GCST90235568 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger C4H2 domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (21117_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger C4H2 domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2044680 GCST90235569 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP cyclohydrolase I feedback regulatory protein level in Chronic kidney disease with hypertension and no diabetes (21118_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP cyclohydrolase 1 feedback regulatory protein in blood serum http://purl.obolibrary.org/obo/OBA_2041687 GCST90235570 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonyl reductase family member 4 level in Chronic kidney disease with hypertension and no diabetes (21119_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 3-oxoacyl-[acyl-carrier-protein] reductase in blood serum http://purl.obolibrary.org/obo/OBA_2040918 GCST90235571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mimitin, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21120_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042542 GCST90235572 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD8-activating enzyme E1 catalytic subunit level in Chronic kidney disease with hypertension and no diabetes (21121_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD8-activating enzyme E1 catalytic subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043981 GCST90235573 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dysbindin domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (21122_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dysbindin domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044239 GCST90235574 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L28, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21123_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L28, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042427 GCST90235575 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Yae1 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (21124_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein YAE1 in blood serum http://purl.obolibrary.org/obo/OBA_2044504 GCST90235576 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin beta A chain level in Chronic kidney disease with hypertension and no diabetes (13738_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 inhibin beta A chain measurement http://www.ebi.ac.uk/efo/EFO_0020469 GCST90234064 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane protein FLRT1 level in Chronic kidney disease with hypertension and no diabetes (13739_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine-rich repeat transmembrane protein FLRT1 measurement http://www.ebi.ac.uk/efo/EFO_0020533 GCST90234065 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted frizzled-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (13740_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90234066 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (13741_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90234067 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-22 level in Chronic kidney disease with hypertension and no diabetes (13742_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90234068 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cullin-4B level in Chronic kidney disease with hypertension and no diabetes (13743_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cullin-4B in blood serum http://purl.obolibrary.org/obo/OBA_2041199 GCST90234069 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-3 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (13744_37) 466 African American individuals NA Illumina [14870897] (imputed) 1 interleukin-3 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020504 GCST90234070 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polycystin-2 level in Chronic kidney disease with hypertension and no diabetes (13745_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234071 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 6 level in Chronic kidney disease with hypertension and no diabetes (13747_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 carbonic anhydrase 6 measurement http://www.ebi.ac.uk/efo/EFO_0008068 GCST90234072 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 8 level in Chronic kidney disease with hypertension and no diabetes (13748_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 8 measurement http://www.ebi.ac.uk/efo/EFO_0008055 GCST90234073 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myocardial zonula adherens protein level in Chronic kidney disease with hypertension and no diabetes (13924_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myocardial zonula adherens protein in blood serum http://purl.obolibrary.org/obo/OBA_2044333 GCST90234074 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RecQ-mediated genome instability protein 1 level in Chronic kidney disease with hypertension and no diabetes (13926_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RecQ-mediated genome instability protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043279 GCST90234075 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal carnitine O-octanoyltransferase level in Chronic kidney disease with hypertension and no diabetes (13929_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisomal carnitine O-octanoyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041151 GCST90234076 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA dC->dU-editing enzyme APOBEC-3G level in Chronic kidney disease with hypertension and no diabetes (13930_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA dC->dU-editing enzyme APOBEC-3G in blood serum http://purl.obolibrary.org/obo/OBA_2044248 GCST90234077 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S proteasome non-ATPase regulatory subunit 9 level in Chronic kidney disease with hypertension and no diabetes (13931_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 26S proteasome non-ATPase regulatory subunit 9 in blood serum http://purl.obolibrary.org/obo/OBA_2043078 GCST90234078 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho guanine nucleotide exchange factor 7 level in Chronic kidney disease with hypertension and no diabetes (13932_45) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Rho guanine nucleotide exchange factor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040661 GCST90234079 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide exchange factor DBS level in Chronic kidney disease with hypertension and no diabetes (13934_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide exchange factor DBS in blood serum http://purl.obolibrary.org/obo/OBA_2042314 GCST90234080 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoglycerate kinase 2 level in Chronic kidney disease with hypertension and no diabetes (13936_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoglycerate kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042860 GCST90234081 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cullin-associated NEDD8-dissociated protein 1 level in Chronic kidney disease with hypertension and no diabetes (13937_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cullin-associated NEDD8-dissociated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040885 GCST90234082 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UTP--glucose-1-phosphate uridylyltransferase level in Chronic kidney disease with hypertension and no diabetes (13939_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UTP--glucose-1-phosphate uridylyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044022 GCST90234083 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prefoldin subunit 4 level in Chronic kidney disease with hypertension and no diabetes (20956_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prefoldin subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042850 GCST90235522 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diphosphoinositol polyphosphate phosphohydrolase 3-alpha level in Chronic kidney disease with hypertension and no diabetes (20957_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diphosphoinositol polyphosphate phosphohydrolase 3-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042663 GCST90235523 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-23 level in Chronic kidney disease with hypertension and no diabetes (20958_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-23 in blood serum http://purl.obolibrary.org/obo/OBA_2043146 GCST90235524 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 18 level in Chronic kidney disease with hypertension and no diabetes (20959_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 18 in blood serum http://purl.obolibrary.org/obo/OBA_2041382 GCST90235525 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Far upstream element-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (20960_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of far upstream element-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041629 GCST90235526 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase 2D level in Chronic kidney disease with hypertension and no diabetes (13623_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone-lysine N-methyltransferase 2D in blood serum http://purl.obolibrary.org/obo/OBA_2042378 GCST90233989 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD kinase level in Chronic kidney disease with hypertension and no diabetes (13624_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NAD kinase in blood serum http://purl.obolibrary.org/obo/OBA_2042498 GCST90233990 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lupus La protein level in Chronic kidney disease with hypertension and no diabetes (13625_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233991 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth factor receptor-bound protein 14 level in Chronic kidney disease with hypertension and no diabetes (13628_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth factor receptor-bound protein 14 in blood serum http://purl.obolibrary.org/obo/OBA_2041784 GCST90233992 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine protease ATG4B level in Chronic kidney disease with hypertension and no diabetes (13629_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine protease ATG4B in blood serum http://purl.obolibrary.org/obo/OBA_2040719 GCST90233993 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoblastoma-binding protein 5 level in Chronic kidney disease with hypertension and no diabetes (13631_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinoblastoma-binding protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043202 GCST90233994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zyxin level in Chronic kidney disease with hypertension and no diabetes (13632_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zyxin in blood serum http://purl.obolibrary.org/obo/OBA_2044224 GCST90233995 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pirin level in Chronic kidney disease with hypertension and no diabetes (13634_209) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pirin in blood serum http://purl.obolibrary.org/obo/OBA_2042900 GCST90233996 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleosome assembly protein 1-like 1 level in Chronic kidney disease with hypertension and no diabetes (13636_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleosome assembly protein 1-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042506 GCST90233997 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. General vesicular transport factor p115 level in Chronic kidney disease with hypertension and no diabetes (13639_101) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of general vesicular transport factor p115 in blood serum http://purl.obolibrary.org/obo/OBA_2044051 GCST90233998 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell lymphoma 6 protein level in Chronic kidney disease with hypertension and no diabetes (13640_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 B-cell lymphoma 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0021933 GCST90233999 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon-induced protein with tetratricopeptide repeats 3 level in Chronic kidney disease with hypertension and no diabetes (13642_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon-induced protein with tetratricopeptide repeats 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044314 GCST90234000 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte growth factor-regulated tyrosine kinase substrate level in Chronic kidney disease with hypertension and no diabetes (13644_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatocyte growth factor-regulated tyrosine kinase substrate in blood serum http://purl.obolibrary.org/obo/OBA_2041870 GCST90234001 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 level in Chronic kidney disease with hypertension and no diabetes (13645_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16 in blood serum http://purl.obolibrary.org/obo/OBA_2041298 GCST90234002 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kv channel-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (13650_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Kv channel-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042089 GCST90234003 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase ZFP91 level in Chronic kidney disease with hypertension and no diabetes (13651_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase ZFP91 in blood serum http://purl.obolibrary.org/obo/OBA_2044182 GCST90234004 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TOM1-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (13652_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TOM1-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043899 GCST90234005 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. O-acetyl-ADP-ribose deacetylase MACROD1 level in Chronic kidney disease with hypertension and no diabetes (13653_335) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribose glycohydrolase MACROD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044388 GCST90234006 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-associated protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (13654_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-associated protein kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040199 GCST90234007 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleolin level in Chronic kidney disease with hypertension and no diabetes (13655_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleolin in blood serum http://purl.obolibrary.org/obo/OBA_2042529 GCST90234008 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional polynucleotide phosphatase/kinase level in Chronic kidney disease with hypertension and no diabetes (13657_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional polynucleotide phosphatase/kinase in blood serum http://purl.obolibrary.org/obo/OBA_2042947 GCST90234009 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor C level in Chronic kidney disease with hypertension and no diabetes (13658_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet-derived growth factor c measurement http://www.ebi.ac.uk/efo/EFO_0020648 GCST90234010 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Manganese-transporting ATPase 13A1 level in Chronic kidney disease with hypertension and no diabetes (13659_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoplasmic reticulum transmembrane helix translocase in blood serum http://purl.obolibrary.org/obo/OBA_2044649 GCST90234011 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-2 level in Chronic kidney disease with hypertension and no diabetes (13660_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiopoietin-2 measurement http://www.ebi.ac.uk/efo/EFO_0006901 GCST90234012 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-D level in Chronic kidney disease with hypertension and no diabetes (13661_193) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin-D measurement http://www.ebi.ac.uk/efo/EFO_0008103 GCST90234013 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin-specific chaperone cofactor E-like protein level in Chronic kidney disease with hypertension and no diabetes (21162_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin-specific chaperone cofactor E-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2043793 GCST90235602 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TBC1 domain family member 13 level in Chronic kidney disease with hypertension and no diabetes (21163_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TBC1 domain family member 13 in blood serum http://purl.obolibrary.org/obo/OBA_2043783 GCST90235603 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein TGIF2LX level in Chronic kidney disease with hypertension and no diabetes (21164_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein TGIF2LX in blood serum http://purl.obolibrary.org/obo/OBA_2043836 GCST90235604 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (21166_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044686 GCST90235605 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylglycerophosphatase and protein-tyrosine phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (21167_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-tyrosine phosphatase mitochondrial 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043100 GCST90235606 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mesoderm development candidate 1 level in Chronic kidney disease with hypertension and no diabetes (21172_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of talin rod domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042341 GCST90235607 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ELAV-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (21173_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ELAV-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041464 GCST90235608 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable cytosolic iron-sulfur protein assembly protein CIAO1 level in Chronic kidney disease with hypertension and no diabetes (21178_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein CIAO1 in blood serum http://purl.obolibrary.org/obo/OBA_2041028 GCST90235609 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PI-PLC X domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (21180_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PI-PLC X domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044398 GCST90235610 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LRP2-binding protein level in Chronic kidney disease with hypertension and no diabetes (21181_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LRP2-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2042232 GCST90235611 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA-splicing endonuclease subunit Sen15 level in Chronic kidney disease with hypertension and no diabetes (21182_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA-splicing endonuclease subunit Sen15 in blood serum http://purl.obolibrary.org/obo/OBA_2043945 GCST90235612 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 10 level in Chronic kidney disease with hypertension and no diabetes (21183_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041379 GCST90235613 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biogenesis of lysosome-related organelles complex 1 subunit 2 level in Chronic kidney disease with hypertension and no diabetes (21184_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of biogenesis of lysosome-related organelles complex 1 subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040806 GCST90235614 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RWD domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (21188_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RWD domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044354 GCST90235615 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleotide-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (21189_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosolic Fe-S cluster assembly factor NUBP1 in blood serum http://purl.obolibrary.org/obo/OBA_2042658 GCST90235616 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 W level in Chronic kidney disease with hypertension and no diabetes (21190_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 W in blood serum http://purl.obolibrary.org/obo/OBA_2044471 GCST90235617 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 21 level in Chronic kidney disease with hypertension and no diabetes (21191_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 21 in blood serum http://purl.obolibrary.org/obo/OBA_2041384 GCST90235618 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-37 level in Chronic kidney disease with hypertension and no diabetes (2723_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-37 measurement http://www.ebi.ac.uk/efo/EFO_0020506 GCST90237062 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin level in Chronic kidney disease with hypertension and no diabetes (2728_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90237063 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MHC class I polypeptide-related sequence A level in Chronic kidney disease with hypertension and no diabetes (2730_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 MHC class I polypeptide-related sequence A measurement http://www.ebi.ac.uk/efo/EFO_0008233 GCST90237064 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADPH--cytochrome P450 reductase level in Chronic kidney disease with hypertension and no diabetes (2731_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 NADPH--cytochrome P450 reductase measurement http://www.ebi.ac.uk/efo/EFO_0008242 GCST90237065 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein NANOG level in Chronic kidney disease with hypertension and no diabetes (2732_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 homeobox protein nanog measurement http://www.ebi.ac.uk/efo/EFO_0020456 GCST90237066 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Natural cytotoxicity triggering receptor 2 level in Chronic kidney disease with hypertension and no diabetes (2734_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 natural cytotoxicity triggering receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020589 GCST90237067 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein NOV homolog level in Chronic kidney disease with hypertension and no diabetes (2737_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein nov homolog measurement http://www.ebi.ac.uk/efo/EFO_0020685 GCST90237068 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 6 level in Chronic kidney disease with hypertension and no diabetes (2741_22) 466 African American individuals NA Illumina [14870897] (imputed) 1 sialic acid-binding Ig-like lectin 6 measurement http://www.ebi.ac.uk/efo/EFO_0008285 GCST90237069 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin lambda-like polypeptide 1 level in Chronic kidney disease with hypertension and no diabetes (6485_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin lambda-like polypeptide 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040340 GCST90238300 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-15 level in Chronic kidney disease with hypertension and no diabetes (6491_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kallikrein-15 in blood serum http://purl.obolibrary.org/obo/OBA_2042127 GCST90238301 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase Z level in Chronic kidney disease with hypertension and no diabetes (6493_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase Z in blood serum http://purl.obolibrary.org/obo/OBA_2041127 GCST90238302 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm acrosome-associated protein 5 level in Chronic kidney disease with hypertension and no diabetes (6494_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm acrosome-associated protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043609 GCST90238303 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelin-1 level in Chronic kidney disease with hypertension and no diabetes (6495_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endothelin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041413 GCST90238304 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein delta homolog 1 level in Chronic kidney disease with hypertension and no diabetes (6496_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein delta homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041313 GCST90238305 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoschisin level in Chronic kidney disease with hypertension and no diabetes (6497_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinoschisin in blood serum http://purl.obolibrary.org/obo/OBA_2043349 GCST90238306 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich motor neuron 1 protein level in Chronic kidney disease with hypertension and no diabetes (6502_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238307 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysyl oxidase homolog 2 level in Chronic kidney disease with hypertension and no diabetes (6504_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysyl oxidase homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042219 GCST90238308 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane emp24 domain-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (6506_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane emp24 domain-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043867 GCST90238309 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neural cell adhesion molecule 2 level in Chronic kidney disease with hypertension and no diabetes (6507_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of neural cell adhesion molecule 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042521 GCST90238310 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretoglobin family 1D member 2 level in Chronic kidney disease with hypertension and no diabetes (6508_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretoglobin family 1D member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043398 GCST90238311 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF128 level in Chronic kidney disease with hypertension and no diabetes (6510_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238312 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM19A4 level in Chronic kidney disease with hypertension and no diabetes (6511_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chemokine-like protein TAFA-4 in blood serum http://purl.obolibrary.org/obo/OBA_2044767 GCST90238313 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kremen protein 1 level in Chronic kidney disease with hypertension and no diabetes (6512_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Kremen protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042136 GCST90238314 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 10 level in Chronic kidney disease with hypertension and no diabetes (6517_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 3B in blood serum http://purl.obolibrary.org/obo/OBA_2041697 GCST90238315 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Appetite-regulating hormone level in Chronic kidney disease with hypertension and no diabetes (6518_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 appetite-regulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0022016 GCST90238316 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix Gla protein level in Chronic kidney disease with hypertension and no diabetes (6520_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of matrix Gla protein in blood serum http://purl.obolibrary.org/obo/OBA_2042364 GCST90238317 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal pentraxin-2 level in Chronic kidney disease with hypertension and no diabetes (6521_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuronal pentraxin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042623 GCST90238318 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Odorant-binding protein 2a level in Chronic kidney disease with hypertension and no diabetes (6526_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of odorant-binding protein 2a in blood serum http://purl.obolibrary.org/obo/OBA_2042688 GCST90238319 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TLR4 interactor with leucine rich repeats level in Chronic kidney disease with hypertension and no diabetes (6527_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238320 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Exostosin-like 2 level in Chronic kidney disease with hypertension and no diabetes (6528_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of exostosin-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041529 GCST90238321 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Opiorphin prepropeptide level in Chronic kidney disease with hypertension and no diabetes (6530_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of opiorphin prepropeptide in blood serum http://purl.obolibrary.org/obo/OBA_2043036 GCST90238322 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM162A level in Chronic kidney disease with hypertension and no diabetes (6531_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM162A in blood serum http://purl.obolibrary.org/obo/OBA_2044409 GCST90238323 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform level in Chronic kidney disease with hypertension and no diabetes (13622_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform in blood serum http://purl.obolibrary.org/obo/OBA_2043010 GCST90233988 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-4 level in Chronic kidney disease with hypertension and no diabetes (13663_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040291 GCST90234014 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit alpha level in Chronic kidney disease with hypertension and no diabetes (13665_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein phosphatase 2A regulatory subunit B'' subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043008 GCST90234015 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase-related protein 10 level in Chronic kidney disease with hypertension and no diabetes (13666_222) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase-related protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020233 GCST90234016 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase receptor TYRO3 level in Chronic kidney disease with hypertension and no diabetes (13668_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase receptor TYRO3 measurement http://www.ebi.ac.uk/efo/EFO_0020829 GCST90234017 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor receptor 3 level in Chronic kidney disease with hypertension and no diabetes (13669_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020390 GCST90234018 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Group IIE secretory phospholipase A2 level in Chronic kidney disease with hypertension and no diabetes (13670_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 group IIe secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020424 GCST90234019 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil elastase level in Chronic kidney disease with hypertension and no diabetes (13671_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 neutrophil elastase measurement http://www.ebi.ac.uk/efo/EFO_0020605 GCST90234020 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 6 level in Chronic kidney disease with hypertension and no diabetes (13672_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90234021 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin beta B chain level in Chronic kidney disease with hypertension and no diabetes (13676_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activin/inhibin beta B chain in blood serum http://purl.obolibrary.org/obo/OBA_2040210 GCST90234022 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor D level in Chronic kidney disease with hypertension and no diabetes (13678_169) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90234023 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NGFI-A-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (13680_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NGFI-A-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042497 GCST90234024 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase II subunit alpha' level in Chronic kidney disease with hypertension and no diabetes (13681_173) 466 African American individuals NA Illumina [14870897] (imputed) 0 casein kinase II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020238 GCST90234025 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage colony-stimulating factor 1 receptor level in Chronic kidney disease with hypertension and no diabetes (13682_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage colony-stimulating factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020547 GCST90234026 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-5 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (13686_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-5 receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040341 GCST90234027 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 1 level in Chronic kidney disease with hypertension and no diabetes (13687_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 1 measurement http://www.ebi.ac.uk/efo/EFO_0008041 GCST90234028 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcyphosin-like protein level in Chronic kidney disease with hypertension and no diabetes (13688_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcyphosin-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2040895 GCST90234029 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ornithine decarboxylase level in Chronic kidney disease with hypertension and no diabetes (13689_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ornithine decarboxylase in blood serum http://purl.obolibrary.org/obo/OBA_2042691 GCST90234030 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biglycan level in Chronic kidney disease with hypertension and no diabetes (13690_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 biglycan measurement http://www.ebi.ac.uk/efo/EFO_0020182 GCST90234031 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium-coupled monocarboxylate transporter 1 level in Chronic kidney disease with hypertension and no diabetes (13691_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium-coupled monocarboxylate transporter 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043539 GCST90234032 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WNT1-inducible-signaling pathway protein 1 level in Chronic kidney disease with hypertension and no diabetes (13692_154) 466 African American individuals NA Illumina [14870897] (imputed) 1 WNT1-inducible-signaling pathway protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008321 GCST90234033 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cerebral dopamine neurotrophic factor level in Chronic kidney disease with hypertension and no diabetes (13693_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90234034 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (13697_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2041770 GCST90234035 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dyslexia-associated protein KIAA0319-like protein level in Chronic kidney disease with hypertension and no diabetes (13698_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dyslexia-associated protein KIAA0319-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2044884 GCST90234036 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostate-specific antigen level in Chronic kidney disease with hypertension and no diabetes (13699_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST90234037 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A2 level in Chronic kidney disease with hypertension and no diabetes (13700_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 annexin A2 measurement http://www.ebi.ac.uk/efo/EFO_0008027 GCST90234038 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 13 level in Chronic kidney disease with hypertension and no diabetes (13701_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-X-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020205 GCST90234039 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxymethylglutaryl-CoA synthase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (13704_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hydroxymethylglutaryl-CoA synthase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041893 GCST90234040 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-12 receptor subunit beta-1 level in Chronic kidney disease with hypertension and no diabetes (13706_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 obsolete_interleukin 12 receptor subunit beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0008170 GCST90234041 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPARC-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (13707_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90234042 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-8 level in Chronic kidney disease with hypertension and no diabetes (13708_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90234043 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plasma protease C1 inhibitor level in Chronic kidney disease with hypertension and no diabetes (13710_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90234044 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Clathrin heavy chain 1 level in Chronic kidney disease with hypertension and no diabetes (13711_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of clathrin heavy chain 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044489 GCST90234045 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granzyme A level in Chronic kidney disease with hypertension and no diabetes (13712_104) 466 African American individuals NA Illumina [14870897] (imputed) 0 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90234046 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-trafficking protein SEC22a level in Chronic kidney disease with hypertension and no diabetes (13713_164) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-trafficking protein SEC22a in blood serum http://purl.obolibrary.org/obo/OBA_2043419 GCST90234047 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ficolin-2 level in Chronic kidney disease with hypertension and no diabetes (13717_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 ficolin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008135 GCST90234048 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase PAK 4 level in Chronic kidney disease with hypertension and no diabetes (13719_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase PAK 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042750 GCST90234049 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myeloblastin level in Chronic kidney disease with hypertension and no diabetes (13720_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90234050 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C9 level in Chronic kidney disease with hypertension and no diabetes (13722_105) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement component C9 measurement http://www.ebi.ac.uk/efo/EFO_0020282 GCST90234051 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-10 level in Chronic kidney disease with hypertension and no diabetes (13723_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90234052 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 19 level in Chronic kidney disease with hypertension and no diabetes (13724_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90234053 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 16 level in Chronic kidney disease with hypertension and no diabetes (13725_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90234054 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-lymphocyte activation antigen CD80 level in Chronic kidney disease with hypertension and no diabetes (13726_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 t-lymphocyte activation antigen CD80 measurement http://www.ebi.ac.uk/efo/EFO_0020761 GCST90234055 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Speckle-type POZ protein level in Chronic kidney disease with hypertension and no diabetes (13727_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of speckle-type POZ protein in blood serum http://purl.obolibrary.org/obo/OBA_2043642 GCST90234056 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum resident protein 29 level in Chronic kidney disease with hypertension and no diabetes (13728_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 endoplasmic reticulum resident protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0020346 GCST90234057 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sideroflexin-5 level in Chronic kidney disease with hypertension and no diabetes (13729_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sideroflexin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043482 GCST90234058 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C7 level in Chronic kidney disease with hypertension and no diabetes (13731_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90234059 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cardiotrophin-1 level in Chronic kidney disease with hypertension and no diabetes (13732_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 cardiotrophin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020235 GCST90234060 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-12 subunit beta level in Chronic kidney disease with hypertension and no diabetes (13733_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-12 subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040279 GCST90234061 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon lambda-1 level in Chronic kidney disease with hypertension and no diabetes (13734_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon lambda-1 measurement http://www.ebi.ac.uk/efo/EFO_0020485 GCST90234062 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rap1 GTPase-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (13735_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rap1 GTPase-activating protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043193 GCST90234063 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alkaline phosphatase, placental-like level in Chronic kidney disease with hypertension and no diabetes (6715_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alkaline phosphatase, germ cell type in blood serum http://purl.obolibrary.org/obo/OBA_2040577 GCST90238385 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transferrin receptor protein 1 level in Chronic kidney disease with hypertension and no diabetes (6895_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238386 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein C1orf162 level in Chronic kidney disease with hypertension and no diabetes (6896_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein C1orf162 in blood serum http://purl.obolibrary.org/obo/OBA_2044847 GCST90238387 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (6897_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040750 GCST90238388 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pterin-4-alpha-carbinolamine dehydratase 2 level in Chronic kidney disease with hypertension and no diabetes (6899_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pterin-4-alpha-carbinolamine dehydratase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042778 GCST90238389 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 J1 level in Chronic kidney disease with hypertension and no diabetes (6900_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 J1 in blood serum http://purl.obolibrary.org/obo/OBA_2043997 GCST90238390 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane neuronal protein 2 level in Chronic kidney disease with hypertension and no diabetes (6904_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat transmembrane neuronal protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042238 GCST90238391 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane and coiled-coil domain-containing protein 5A level in Chronic kidney disease with hypertension and no diabetes (6907_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane and coiled-coil domain-containing protein 5A in blood serum http://purl.obolibrary.org/obo/OBA_2044612 GCST90238392 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase level in Chronic kidney disease with hypertension and no diabetes (6909_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042357 GCST90238393 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 6 member A level in Chronic kidney disease with hypertension and no diabetes (6911_103) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 6 member A in blood serum http://purl.obolibrary.org/obo/OBA_2040329 GCST90238394 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium uptake protein 3, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (6912_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium uptake protein 3, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044736 GCST90238395 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amphoterin-induced protein 2 level in Chronic kidney disease with hypertension and no diabetes (6914_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 amphoterin-induced protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021949 GCST90238396 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (6917_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044677 GCST90238397 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cholecystokinin level in Chronic kidney disease with hypertension and no diabetes (6918_183) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cholecystokinin in blood serum http://purl.obolibrary.org/obo/OBA_2040929 GCST90238398 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemoglobin subunit zeta level in Chronic kidney disease with hypertension and no diabetes (6919_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of hemoglobin subunit zeta in blood serum http://purl.obolibrary.org/obo/OBA_2041843 GCST90238399 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDNF family receptor alpha-like level in Chronic kidney disease with hypertension and no diabetes (6920_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GDNF family receptor alpha-like in blood serum http://purl.obolibrary.org/obo/OBA_2044417 GCST90238400 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4-galactosyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (6921_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,4-galactosyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040758 GCST90238401 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 level in Chronic kidney disease with hypertension and no diabetes (6923_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042929 GCST90238402 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-8 level in Chronic kidney disease with hypertension and no diabetes (6925_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-8 in blood serum http://purl.obolibrary.org/obo/OBA_2043591 GCST90238403 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (6927_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042539 GCST90238404 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sia-alpha-2,3-Gal-beta-1,4-GlcNAc-R:alpha 2,8-sialyltransferase level in Chronic kidney disease with hypertension and no diabetes (6929_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sia-alpha-2,3-Gal-beta-1,4-GlcNAc-R:alpha 2,8-sialyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043683 GCST90238405 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-2,8-sialyltransferase 8F level in Chronic kidney disease with hypertension and no diabetes (6930_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-2,8-sialyltransferase 8F in blood serum http://purl.obolibrary.org/obo/OBA_2043685 GCST90238406 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cancer/testis antigen 1 level in Chronic kidney disease with hypertension and no diabetes (6931_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cancer/testis antigen 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041181 GCST90238407 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-5 level in Chronic kidney disease with hypertension and no diabetes (6932_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin alpha-5 in blood serum http://purl.obolibrary.org/obo/OBA_2042047 GCST90238408 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L34, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (6933_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 39S ribosomal protein L34, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042430 GCST90238409 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin-like protein KIF3A level in Chronic kidney disease with hypertension and no diabetes (13961_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of kinesin-like protein KIF3A in blood serum http://purl.obolibrary.org/obo/OBA_2042099 GCST90234098 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-interacting protein level in Chronic kidney disease with hypertension and no diabetes (13963_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Toll-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043897 GCST90234099 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myomesin-3 level in Chronic kidney disease with hypertension and no diabetes (13966_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myomesin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042490 GCST90234100 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin reductase 1, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (13967_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of thioredoxin reductase 1, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2043974 GCST90234101 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Importin subunit alpha-7 level in Chronic kidney disease with hypertension and no diabetes (13969_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of importin subunit alpha-7 in blood serum http://purl.obolibrary.org/obo/OBA_2042135 GCST90234102 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 17-beta-hydroxysteroid dehydrogenase 14 level in Chronic kidney disease with hypertension and no diabetes (13972_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 17-beta-hydroxysteroid dehydrogenase 14 in blood serum http://purl.obolibrary.org/obo/OBA_2041940 GCST90234103 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin--tyrosine ligase level in Chronic kidney disease with hypertension and no diabetes (13973_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin--tyrosine ligase in blood serum http://purl.obolibrary.org/obo/OBA_2043956 GCST90234104 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Liprin-alpha-1 level in Chronic kidney disease with hypertension and no diabetes (13975_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of liprin-alpha-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042984 GCST90234105 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho guanine nucleotide exchange factor 1 level in Chronic kidney disease with hypertension and no diabetes (13976_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho guanine nucleotide exchange factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040657 GCST90234106 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRCA1-associated RING domain protein 1 level in Chronic kidney disease with hypertension and no diabetes (13977_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRCA1-associated RING domain protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040777 GCST90234107 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-box transcription factor TBX3 level in Chronic kidney disease with hypertension and no diabetes (13978_122) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-box transcription factor TBX3 in blood serum http://purl.obolibrary.org/obo/OBA_2043797 GCST90234108 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anion exchange transporter level in Chronic kidney disease with hypertension and no diabetes (13979_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anion exchange transporter in blood serum http://purl.obolibrary.org/obo/OBA_2043531 GCST90234109 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 18 level in Chronic kidney disease with hypertension and no diabetes (13982_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 18 in blood serum http://purl.obolibrary.org/obo/OBA_2043257 GCST90234110 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent RNA helicase DDX25 level in Chronic kidney disease with hypertension and no diabetes (13984_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent RNA helicase DDX25 in blood serum http://purl.obolibrary.org/obo/OBA_2041260 GCST90234111 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase SMURF2 level in Chronic kidney disease with hypertension and no diabetes (13985_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase SMURF2 in blood serum http://purl.obolibrary.org/obo/OBA_2040215 GCST90234112 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LanC-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (13986_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase LANCL1 in blood serum http://purl.obolibrary.org/obo/OBA_2042161 GCST90234113 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NmrA-like family domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (13988_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of NmrA-like family domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044335 GCST90234114 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyruvate carboxylase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (13990_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyruvate carboxylase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042775 GCST90234115 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4 gamma 3 level in Chronic kidney disease with hypertension and no diabetes (13991_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 4 gamma 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041457 GCST90234116 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-fusing ATPase level in Chronic kidney disease with hypertension and no diabetes (13992_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-fusing ATPase in blood serum http://purl.obolibrary.org/obo/OBA_2042645 GCST90234117 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Band 4.1-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (13993_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of band 4.1-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041486 GCST90234118 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. rRNA 2'-O-methyltransferase fibrillarin level in Chronic kidney disease with hypertension and no diabetes (13994_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90234119 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphopantothenoylcysteine decarboxylase level in Chronic kidney disease with hypertension and no diabetes (13996_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphopantothenoylcysteine decarboxylase in blood serum http://purl.obolibrary.org/obo/OBA_2042982 GCST90234120 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenylosuccinate synthetase isozyme 1 level in Chronic kidney disease with hypertension and no diabetes (13998_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adenylosuccinate synthetase isozyme 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040527 GCST90234121 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dedicator of cytokinesis protein 9 level in Chronic kidney disease with hypertension and no diabetes (14002_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dedicator of cytokinesis protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2041341 GCST90234122 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleotide pyrophosphatase/phosphodiesterase family member 5 level in Chronic kidney disease with hypertension and no diabetes (6556_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ectonucleotide pyrophosphatase/phosphodiesterase family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041481 GCST90238335 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 15 level in Chronic kidney disease with hypertension and no diabetes (6557_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 15 in blood serum http://purl.obolibrary.org/obo/OBA_2044404 GCST90238336 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collectin-10 level in Chronic kidney disease with hypertension and no diabetes (6558_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collectin-10 in blood serum http://purl.obolibrary.org/obo/OBA_2041089 GCST90238337 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ig Kappa chain V-I region HK102- like level in Chronic kidney disease with hypertension and no diabetes (6561_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin kappa variable 1-5 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044896 GCST90238338 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (6563_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90238339 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUB domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (6565_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CUB domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040956 GCST90238340 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HEPACAM family member 2 level in Chronic kidney disease with hypertension and no diabetes (6568_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238341 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(XIII) chain level in Chronic kidney disease with hypertension and no diabetes (6570_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(XIII) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041082 GCST90238342 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C17orf78 level in Chronic kidney disease with hypertension and no diabetes (6571_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238343 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane neuronal protein 4 level in Chronic kidney disease with hypertension and no diabetes (6572_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238344 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fas apoptotic inhibitory molecule 3 level in Chronic kidney disease with hypertension and no diabetes (6574_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fas apoptotic inhibitory molecule 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041546 GCST90238345 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADAMTS-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (6575_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADAMTS-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040506 GCST90238346 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ecto-ADP-ribosyltransferase 4 level in Chronic kidney disease with hypertension and no diabetes (6576_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ecto-ADP-ribosyltransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040339 GCST90238347 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Laminin subunit alpha-4 level in Chronic kidney disease with hypertension and no diabetes (6577_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of laminin subunit alpha-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042158 GCST90238348 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenomodulin level in Chronic kidney disease with hypertension and no diabetes (6578_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tenomodulin in blood serum http://purl.obolibrary.org/obo/OBA_2043892 GCST90238349 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy zone protein level in Chronic kidney disease with hypertension and no diabetes (6580_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pregnancy zone protein in blood serum http://purl.obolibrary.org/obo/OBA_2043127 GCST90238350 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Z-dependent protease inhibitor level in Chronic kidney disease with hypertension and no diabetes (6583_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein Z-dependent protease inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0021849 GCST90238351 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sarcoplasmic reticulum histidine-rich calcium-binding protein level in Chronic kidney disease with hypertension and no diabetes (6584_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sarcoplasmic reticulum histidine-rich calcium-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2041926 GCST90238352 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 11 level in Chronic kidney disease with hypertension and no diabetes (6586_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2040495 GCST90238353 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and fibronectin type-III domain-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (6587_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and fibronectin type-III domain-containing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044732 GCST90238354 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropilin-2 level in Chronic kidney disease with hypertension and no diabetes (6590_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuropilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042642 GCST90238355 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (6593_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041665 GCST90238356 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SAYSvFN domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (6594_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SAYSvFN domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044702 GCST90238357 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane protein FAM174A level in Chronic kidney disease with hypertension and no diabetes (6597_24) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of membrane protein FAM174A in blood serum http://purl.obolibrary.org/obo/OBA_2044467 GCST90238358 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein APCDD1 level in Chronic kidney disease with hypertension and no diabetes (6599_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein APCDD1 in blood serum http://purl.obolibrary.org/obo/OBA_2040615 GCST90238359 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BMP and activin membrane-bound inhibitor homolog level in Chronic kidney disease with hypertension and no diabetes (6935_123) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238410 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein TMEPAI level in Chronic kidney disease with hypertension and no diabetes (6936_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein TMEPAI in blood serum http://purl.obolibrary.org/obo/OBA_2042941 GCST90238411 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C1orf43 level in Chronic kidney disease with hypertension and no diabetes (6937_251) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein C1orf43 in blood serum http://purl.obolibrary.org/obo/OBA_2044888 GCST90238412 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin gamma-A12 level in Chronic kidney disease with hypertension and no diabetes (6938_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin gamma-A12 in blood serum http://purl.obolibrary.org/obo/OBA_2042794 GCST90238413 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctophilin-1 level in Chronic kidney disease with hypertension and no diabetes (6940_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of junctophilin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042074 GCST90238414 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfatase-modifying factor 1 level in Chronic kidney disease with hypertension and no diabetes (6941_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of formylglycine-generating enzyme in blood serum http://purl.obolibrary.org/obo/OBA_2043732 GCST90238415 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Type 2 lactosamine alpha-2,3-sialyltransferase level in Chronic kidney disease with hypertension and no diabetes (6947_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of type 2 lactosamine alpha-2,3-sialyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043672 GCST90238416 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyphosphoinositide phosphatase level in Chronic kidney disease with hypertension and no diabetes (6948_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyphosphoinositide phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2044524 GCST90238417 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acid-sensing ion channel 4 level in Chronic kidney disease with hypertension and no diabetes (6951_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acid-sensing ion channel 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040476 GCST90238418 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-1 level in Chronic kidney disease with hypertension and no diabetes (6955_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043582 GCST90238419 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pancreatic lipase-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (6957_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pancreatic lipase-related protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042950 GCST90238420 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-interferon-inducible protein 16 level in Chronic kidney disease with hypertension and no diabetes (13940_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234084 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phenylalanine--tRNA ligase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (13941_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phenylalanine--tRNA ligase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041549 GCST90234085 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPRY domain-containing SOCS box protein 1 level in Chronic kidney disease with hypertension and no diabetes (13942_140) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SPRY domain-containing SOCS box protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043646 GCST90234086 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein dpy-30 homolog level in Chronic kidney disease with hypertension and no diabetes (13943_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein dpy-30 in blood serum http://purl.obolibrary.org/obo/OBA_2041355 GCST90234087 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfotransferase 1A3 level in Chronic kidney disease with hypertension and no diabetes (13944_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 1A3 in blood serum http://purl.obolibrary.org/obo/OBA_2044235 GCST90234088 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable ATP-dependent RNA helicase DDX23 level in Chronic kidney disease with hypertension and no diabetes (13946_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable ATP-dependent RNA helicase DDX23 in blood serum http://purl.obolibrary.org/obo/OBA_2044277 GCST90234089 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal NADH pyrophosphatase NUDT12 level in Chronic kidney disease with hypertension and no diabetes (13947_371) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NAD-capped RNA hydrolase NUDT12 in blood serum http://purl.obolibrary.org/obo/OBA_2042665 GCST90234090 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-aminobutyric acid type B receptor subunit 2 level in Chronic kidney disease with hypertension and no diabetes (13948_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234091 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen type IV alpha-3-binding protein level in Chronic kidney disease with hypertension and no diabetes (13950_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234092 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucosamine 6-phosphate N-acetyltransferase level in Chronic kidney disease with hypertension and no diabetes (13954_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glucosamine 6-phosphate N-acetyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041757 GCST90234093 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Death-associated protein kinase 1 level in Chronic kidney disease with hypertension and no diabetes (13955_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of death-associated protein kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041229 GCST90234094 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable RNA-binding protein 46 level in Chronic kidney disease with hypertension and no diabetes (13958_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable RNA-binding protein 46 in blood serum http://purl.obolibrary.org/obo/OBA_2044502 GCST90234095 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosol aminopeptidase level in Chronic kidney disease with hypertension and no diabetes (13959_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosol aminopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2042163 GCST90234096 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (13960_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040534 GCST90234097 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RELT-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (6600_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RELT-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043236 GCST90238360 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anosmin-1 level in Chronic kidney disease with hypertension and no diabetes (6603_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anosmin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042081 GCST90238361 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein NDNF level in Chronic kidney disease with hypertension and no diabetes (6604_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein NDNF in blood serum http://purl.obolibrary.org/obo/OBA_2044713 GCST90238362 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein complex acid labile subunit level in Chronic kidney disease with hypertension and no diabetes (6605_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-like growth factor-binding protein complex acid labile chain in blood serum http://purl.obolibrary.org/obo/OBA_2041989 GCST90238363 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metastasis-suppressor KiSS-1 level in Chronic kidney disease with hypertension and no diabetes (6606_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of metastasis-suppressor KiSS-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042112 GCST90238364 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2',3'-cyclic-nucleotide 3'-phosphodiesterase level in Chronic kidney disease with hypertension and no diabetes (6609_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 2',3'-cyclic-nucleotide 3'-phosphodiesterase in blood serum http://purl.obolibrary.org/obo/OBA_2041069 GCST90238365 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRICHOS domain-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (6612_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRICHOS domain-containing protein 5 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044906 GCST90238366 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fc receptor-like protein 6 level in Chronic kidney disease with hypertension and no diabetes (6617_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fc receptor-like protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041565 GCST90238367 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (6620_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042206 GCST90238368 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apelin level in Chronic kidney disease with hypertension and no diabetes (6622_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apelin in blood serum http://purl.obolibrary.org/obo/OBA_2040616 GCST90238369 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-11 level in Chronic kidney disease with hypertension and no diabetes (6624_94) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Wnt-11 in blood serum http://purl.obolibrary.org/obo/OBA_2044139 GCST90238370 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATPase family AAA domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (6625_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of outer mitochondrial transmembrane helix translocase in blood serum http://purl.obolibrary.org/obo/OBA_2044253 GCST90238371 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 12 level in Chronic kidney disease with hypertension and no diabetes (6626_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 12 in blood serum http://purl.obolibrary.org/obo/OBA_2041022 GCST90238372 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive pancreatic lipase-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (6627_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pancreatic lipase-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042949 GCST90238373 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 1 level in Chronic kidney disease with hypertension and no diabetes (6629_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041265 GCST90238374 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(IX) chain level in Chronic kidney disease with hypertension and no diabetes (6631_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(IX) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041087 GCST90238375 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uroplakin-3b-like protein level in Chronic kidney disease with hypertension and no diabetes (6633_43) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of uroplakin-3b-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044506 GCST90238376 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PolyUbiquitin K48-linked level in Chronic kidney disease with hypertension and no diabetes (6641_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 polyUbiquitin K48-linked measurement http://www.ebi.ac.uk/efo/EFO_0022007 GCST90238377 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Periostin level in Chronic kidney disease with hypertension and no diabetes (6645_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90238378 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PolyUbiquitin K63-linked level in Chronic kidney disease with hypertension and no diabetes (6647_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 polyUbiquitin K63-linked measurement http://www.ebi.ac.uk/efo/EFO_0022008 GCST90238379 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin-1 level in Chronic kidney disease with hypertension and no diabetes (6649_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 netrin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022009 GCST90238380 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PolyUbiquitin K48-linked level in Chronic kidney disease with hypertension and no diabetes (6651_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 polyUbiquitin K48-linked measurement http://www.ebi.ac.uk/efo/EFO_0022007 GCST90238381 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte surface antigen CD47 level in Chronic kidney disease with hypertension and no diabetes (6653_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 leukocyte surface antigen CD47 measurement http://www.ebi.ac.uk/efo/EFO_0022010 GCST90238382 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alkaline phosphatase, placental-like level in Chronic kidney disease with hypertension and no diabetes (6706_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alkaline phosphatase, germ cell type in blood serum http://purl.obolibrary.org/obo/OBA_2040577 GCST90238383 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 11 level in Chronic kidney disease with hypertension and no diabetes (6713_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of low-density lipoprotein receptor-related protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042229 GCST90238384 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 14 level in Chronic kidney disease with hypertension and no diabetes (2900_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 14 measurement http://www.ebi.ac.uk/efo/EFO_0008042 GCST90237145 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-4 level in Chronic kidney disease with hypertension and no diabetes (2906_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin 4 measurement http://www.ebi.ac.uk/efo/EFO_0008184 GCST90237146 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Midkine level in Chronic kidney disease with hypertension and no diabetes (2911_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 midkine measurement http://www.ebi.ac.uk/efo/EFO_0020571 GCST90237147 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 23 level in Chronic kidney disease with hypertension and no diabetes (2913_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 23 measurement http://www.ebi.ac.uk/efo/EFO_0008049 GCST90237148 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proliferating cell nuclear antigen level in Chronic kidney disease with hypertension and no diabetes (2915_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 proliferating cell nuclear antigen measurement http://www.ebi.ac.uk/efo/EFO_0020657 GCST90237149 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 11 level in Chronic kidney disease with hypertension and no diabetes (2917_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 11 measurement http://www.ebi.ac.uk/efo/EFO_0010617 GCST90237150 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plasminogen activator inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (2925_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 plasminogen activator inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0004792 GCST90237151 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein E (isoform E4) level in Chronic kidney disease with hypertension and no diabetes (2938_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 apolipoprotein E (isoform E4) measurement http://www.ebi.ac.uk/efo/EFO_0020158 GCST90237152 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Artemin level in Chronic kidney disease with hypertension and no diabetes (2939_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 artemin measurement http://www.ebi.ac.uk/efo/EFO_0020162 GCST90237153 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c level in Chronic kidney disease with hypertension and no diabetes (2942_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytochrome C measurement http://www.ebi.ac.uk/efo/EFO_0020302 GCST90237154 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome P450 3A4 level in Chronic kidney disease with hypertension and no diabetes (2943_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 cytochrome p450 3a4 measurement http://www.ebi.ac.uk/efo/EFO_0020303 GCST90237155 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroblastoma suppressor of tumorigenicity 1 level in Chronic kidney disease with hypertension and no diabetes (2944_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuroblastoma suppressor of tumorigenicity 1 measurement http://www.ebi.ac.uk/efo/EFO_0020598 GCST90237156 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor D level in Chronic kidney disease with hypertension and no diabetes (2946_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement factor D measurement http://www.ebi.ac.uk/efo/EFO_0020283 GCST90237157 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth hormone receptor level in Chronic kidney disease with hypertension and no diabetes (2948_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 growth hormone receptor measurement http://www.ebi.ac.uk/efo/EFO_0020426 GCST90237158 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deoxyribonuclease-2-beta level in Chronic kidney disease with hypertension and no diabetes (6533_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deoxyribonuclease-2-beta in blood serum http://purl.obolibrary.org/obo/OBA_2041333 GCST90238324 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative phospholipase B-like 2 level in Chronic kidney disease with hypertension and no diabetes (6536_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative phospholipase B-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044345 GCST90238325 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein KIAA2013 level in Chronic kidney disease with hypertension and no diabetes (6538_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein KIAA2013 in blood serum http://purl.obolibrary.org/obo/OBA_2044840 GCST90238326 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolactin-releasing peptide level in Chronic kidney disease with hypertension and no diabetes (6543_182) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prolactin-releasing peptide in blood serum http://purl.obolibrary.org/obo/OBA_2043032 GCST90238327 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C-binding protein NELL1 level in Chronic kidney disease with hypertension and no diabetes (6544_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein kinase C-binding protein NELL1 in blood serum http://purl.obolibrary.org/obo/OBA_2042557 GCST90238328 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Major prion protein level in Chronic kidney disease with hypertension and no diabetes (6545_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of major prion protein in blood serum http://purl.obolibrary.org/obo/OBA_2040349 GCST90238329 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dickkopf-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (6546_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dickkopf-related protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041306 GCST90238330 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protease serine 11D level in Chronic kidney disease with hypertension and no diabetes (6547_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protease serine 11D in blood serum http://purl.obolibrary.org/obo/OBA_2043883 GCST90238331 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 4 level in Chronic kidney disease with hypertension and no diabetes (6550_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of intercellular adhesion molecule 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040277 GCST90238332 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cilia- and flagella-associated protein 45 level in Chronic kidney disease with hypertension and no diabetes (6553_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cilia- and flagella-associated protein 45 in blood serum http://purl.obolibrary.org/obo/OBA_2044260 GCST90238333 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stomatin-like protein 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (6555_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stomatin-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043707 GCST90238334 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 3-like 1 level in Chronic kidney disease with hypertension and no diabetes (2783_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 3-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0008052 GCST90237095 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 8 level in Chronic kidney disease with hypertension and no diabetes (2785_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 8 measurement http://www.ebi.ac.uk/efo/EFO_0008055 GCST90237096 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromelysin-1 level in Chronic kidney disease with hypertension and no diabetes (2788_55) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of stromelysin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042390 GCST90237097 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Superoxide dismutase [Cu-Zn] level in Chronic kidney disease with hypertension and no diabetes (2794_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of superoxide dismutase [Cu-Zn] in blood serum http://purl.obolibrary.org/obo/OBA_2043594 GCST90237098 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiotensin-converting enzyme 2 level in Chronic kidney disease with hypertension and no diabetes (2805_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiotensin-converting enzyme 2 measurement http://www.ebi.ac.uk/efo/EFO_0020150 GCST90237099 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activin receptor type-1B level in Chronic kidney disease with hypertension and no diabetes (2806_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 activin receptor type-1B measurement http://www.ebi.ac.uk/efo/EFO_0020127 GCST90237100 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A disintegrin and metalloproteinase with thrombospondin motifs 4 level in Chronic kidney disease with hypertension and no diabetes (2809_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 4 measurement http://www.ebi.ac.uk/efo/EFO_0020124 GCST90237101 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Agouti-related protein level in Chronic kidney disease with hypertension and no diabetes (2813_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 Agouti-related protein measurement http://www.ebi.ac.uk/efo/EFO_0008016 GCST90237102 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Basal Cell Adhesion Molecule level in Chronic kidney disease with hypertension and no diabetes (2816_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 basal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008032 GCST90237103 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-5 level in Chronic kidney disease with hypertension and no diabetes (2819_23) 466 African American individuals NA Illumina [14870897] (imputed) 1 cadherin-5 measurement http://www.ebi.ac.uk/efo/EFO_0008060 GCST90237104 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COMM domain-containing protein 7 level in Chronic kidney disease with hypertension and no diabetes (2823_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 COMM domain-containing protein 7 measurement http://www.ebi.ac.uk/efo/EFO_0020273 GCST90237105 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectodysplasin-A, secreted form level in Chronic kidney disease with hypertension and no diabetes (2826_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 ectodysplasin-a, secreted form measurement http://www.ebi.ac.uk/efo/EFO_0020341 GCST90237106 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fractalkine level in Chronic kidney disease with hypertension and no diabetes (2827_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 fractalkine measurement http://www.ebi.ac.uk/efo/EFO_0020395 GCST90237107 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kunitz-type protease inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (2828_82) 466 African American individuals NA Illumina [14870897] (imputed) 2 Kunitz-type protease inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008199 GCST90237108 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-27 level in Chronic kidney disease with hypertension and no diabetes (2829_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-27 measurement http://www.ebi.ac.uk/efo/EFO_0010916 GCST90237109 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-11 level in Chronic kidney disease with hypertension and no diabetes (2831_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90237110 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-4 level in Chronic kidney disease with hypertension and no diabetes (2833_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-4 measurement http://www.ebi.ac.uk/efo/EFO_0020514 GCST90237111 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-8 level in Chronic kidney disease with hypertension and no diabetes (2834_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-8 measurement http://www.ebi.ac.uk/efo/EFO_0020516 GCST90237112 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. X-ray repair cross-complementing protein 6 level in Chronic kidney disease with hypertension and no diabetes (2835_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 x-ray repair cross-complementing protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020855 GCST90237113 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil gelatinase-associated lipocalin level in Chronic kidney disease with hypertension and no diabetes (2836_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 neutrophil gelatinase-associated lipocalin measurement http://www.ebi.ac.uk/efo/EFO_0021964 GCST90237114 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte growth factor receptor level in Chronic kidney disease with hypertension and no diabetes (2837_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 hepatocyte growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0008153 GCST90237115 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-17 level in Chronic kidney disease with hypertension and no diabetes (2838_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrix metalloproteinase-17 measurement http://www.ebi.ac.uk/efo/EFO_0020560 GCST90237116 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 4 level in Chronic kidney disease with hypertension and no diabetes (2839_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020796 GCST90237117 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted frizzled-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (2841_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 Secreted frizzled-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008277 GCST90237118 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kunitz-type protease inhibitor 2 level in Chronic kidney disease with hypertension and no diabetes (2843_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 Kunitz-type protease inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008200 GCST90237119 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase receptor Tie-1, soluble level in Chronic kidney disease with hypertension and no diabetes (2844_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 tyrosine-protein kinase receptor Tie-1, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008312 GCST90237120 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin+1, truncated mutation for UbB level in Chronic kidney disease with hypertension and no diabetes (2846_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin+1, truncated mutation for UBB measurement http://www.ebi.ac.uk/efo/EFO_0020844 GCST90237121 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Wnt inhibitory factor 1 level in Chronic kidney disease with hypertension and no diabetes (2848_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 wnt inhibitory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020853 GCST90237122 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Allograft inflammatory factor 1 level in Chronic kidney disease with hypertension and no diabetes (2849_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 allograft inflammatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020135 GCST90237123 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C5a anaphylatoxin level in Chronic kidney disease with hypertension and no diabetes (2851_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 C5a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020208 GCST90237124 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase Chk1 level in Chronic kidney disease with hypertension and no diabetes (2853_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase Chk1 measurement http://www.ebi.ac.uk/efo/EFO_0021965 GCST90237125 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 3 level in Chronic kidney disease with hypertension and no diabetes (2855_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020579 GCST90237126 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucocorticoid receptor level in Chronic kidney disease with hypertension and no diabetes (2857_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 glucocorticoid receptor measurement http://www.ebi.ac.uk/efo/EFO_0020405 GCST90237127 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone acetyltransferase type B catalytic subunit level in Chronic kidney disease with hypertension and no diabetes (2858_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone acetyltransferase type b catalytic subunit measurement http://www.ebi.ac.uk/efo/EFO_0020452 GCST90237128 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone deacetylase 8 level in Chronic kidney disease with hypertension and no diabetes (2859_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone deacetylase 8 measurement http://www.ebi.ac.uk/efo/EFO_0020453 GCST90237129 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Importin subunit alpha-1 level in Chronic kidney disease with hypertension and no diabetes (2860_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 importin subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020467 GCST90237130 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity mitogen-activated protein kinase kinase 1 level in Chronic kidney disease with hypertension and no diabetes (2864_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 dual specificity mitogen-activated protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020335 GCST90237131 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RAC-alpha serine/threonine-protein kinase level in Chronic kidney disease with hypertension and no diabetes (2867_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RAC-alpha serine/threonine-protein kinase in blood serum http://purl.obolibrary.org/obo/OBA_2040400 GCST90237132 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C delta type level in Chronic kidney disease with hypertension and no diabetes (2869_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein kinase c delta type measurement http://www.ebi.ac.uk/efo/EFO_0020679 GCST90237133 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related C3 botulinum toxin substrate 1 level in Chronic kidney disease with hypertension and no diabetes (2870_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 ras-related c3 botulinum toxin substrate 1 measurement http://www.ebi.ac.uk/efo/EFO_0020699 GCST90237134 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA repair protein RAD51 homolog 1 level in Chronic kidney disease with hypertension and no diabetes (2871_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 DNA repair protein rad51 homolog 1 measurement http://www.ebi.ac.uk/efo/EFO_0020330 GCST90237135 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TATA-box-binding protein level in Chronic kidney disease with hypertension and no diabetes (2875_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 tata-box-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0020764 GCST90237136 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA topoisomerase 1 level in Chronic kidney disease with hypertension and no diabetes (2876_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 DNA topoisomerase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020331 GCST90237137 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SUMO-conjugating enzyme UBC9 level in Chronic kidney disease with hypertension and no diabetes (2877_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 sumo-conjugating enzyme UBC9 measurement http://www.ebi.ac.uk/efo/EFO_0020757 GCST90237138 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase Yes level in Chronic kidney disease with hypertension and no diabetes (2878_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase YES measurement http://www.ebi.ac.uk/efo/EFO_0020832 GCST90237139 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1-antichymotrypsin level in Chronic kidney disease with hypertension and no diabetes (2879_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-1-antichymotrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008019 GCST90237140 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C7 level in Chronic kidney disease with hypertension and no diabetes (2888_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement component C7 measurement http://www.ebi.ac.uk/efo/EFO_0008093 GCST90237141 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cardiotrophin-1 level in Chronic kidney disease with hypertension and no diabetes (2889_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 cardiotrophin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020235 GCST90237142 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 28 level in Chronic kidney disease with hypertension and no diabetes (2890_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 28 measurement http://www.ebi.ac.uk/efo/EFO_0020199 GCST90237143 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell receptor CD22 level in Chronic kidney disease with hypertension and no diabetes (2891_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 B-cell receptor CD22 measurement http://www.ebi.ac.uk/efo/EFO_0020171 GCST90237144 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 7 level in Chronic kidney disease with hypertension and no diabetes (2742_68) 466 African American individuals NA Illumina [14870897] (imputed) 1 sialic acid-binding ig-like lectin 7 measurement http://www.ebi.ac.uk/efo/EFO_0020739 GCST90237070 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sonic hedgehog protein level in Chronic kidney disease with hypertension and no diabetes (2743_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 sonic hedgehog protein measurement http://www.ebi.ac.uk/efo/EFO_0020746 GCST90237071 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin G level in Chronic kidney disease with hypertension and no diabetes (2744_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 immunoglobulin G measurement http://www.ebi.ac.uk/efo/EFO_0020465 GCST90237072 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine receptor-like factor 2 level in Chronic kidney disease with hypertension and no diabetes (2746_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytokine receptor-like factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020306 GCST90237073 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2D ligand 3 level in Chronic kidney disease with hypertension and no diabetes (2747_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UL16-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044030 GCST90237074 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activin A level in Chronic kidney disease with hypertension and no diabetes (2748_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activin/inhibin beta A chain in blood serum http://purl.obolibrary.org/obo/OBA_2040209 GCST90237075 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein A-I level in Chronic kidney disease with hypertension and no diabetes (2750_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apolipoprotein A-I in blood serum http://purl.obolibrary.org/obo/OBA_2040620 GCST90237076 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Azurocidin level in Chronic kidney disease with hypertension and no diabetes (2751_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 azurocidin measurement http://www.ebi.ac.uk/efo/EFO_0020170 GCST90237077 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q subcomponent level in Chronic kidney disease with hypertension and no diabetes (2753_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C1q subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008089 GCST90237078 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C3 level in Chronic kidney disease with hypertension and no diabetes (2754_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C3 measurement http://www.ebi.ac.uk/efo/EFO_0004983 GCST90237079 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C3a anaphylatoxin des Arginine level in Chronic kidney disease with hypertension and no diabetes (2755_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 C3a anaphylatoxin des arginine measurement http://www.ebi.ac.uk/efo/EFO_0020206 GCST90237080 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM107A level in Chronic kidney disease with hypertension and no diabetes (2760_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein fam107a measurement http://www.ebi.ac.uk/efo/EFO_0020673 GCST90237081 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 18 level in Chronic kidney disease with hypertension and no diabetes (2761_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 18 measurement http://www.ebi.ac.uk/efo/EFO_0020380 GCST90237082 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 19 level in Chronic kidney disease with hypertension and no diabetes (2762_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 19 measurement http://www.ebi.ac.uk/efo/EFO_0010782 GCST90237083 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 20 level in Chronic kidney disease with hypertension and no diabetes (2763_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 20 measurement http://www.ebi.ac.uk/efo/EFO_0020381 GCST90237084 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 11/8 level in Chronic kidney disease with hypertension and no diabetes (2765_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 growth/differentiation factor 11/8 measurement http://www.ebi.ac.uk/efo/EFO_0021962 GCST90237085 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemopexin level in Chronic kidney disease with hypertension and no diabetes (2768_56) 466 African American individuals NA Illumina [14870897] (imputed) 1 hemopexin measurement http://www.ebi.ac.uk/efo/EFO_0008149 GCST90237086 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 1 level in Chronic kidney disease with hypertension and no diabetes (2770_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 1 measurement http://www.ebi.ac.uk/efo/EFO_0008041 GCST90237087 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (2771_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020474 GCST90237088 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-10 level in Chronic kidney disease with hypertension and no diabetes (2773_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-10 measurement http://www.ebi.ac.uk/efo/EFO_0020488 GCST90237089 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-16 level in Chronic kidney disease with hypertension and no diabetes (2774_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-16 in blood serum http://purl.obolibrary.org/obo/OBA_2040282 GCST90237090 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17F level in Chronic kidney disease with hypertension and no diabetes (2775_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17F measurement http://www.ebi.ac.uk/efo/EFO_0021963 GCST90237091 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-22 level in Chronic kidney disease with hypertension and no diabetes (2778_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-22 measurement http://www.ebi.ac.uk/efo/EFO_0020498 GCST90237092 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactotransferrin level in Chronic kidney disease with hypertension and no diabetes (2780_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 lactotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020526 GCST90237093 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 4-like level in Chronic kidney disease with hypertension and no diabetes (2781_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 4-like measurement http://www.ebi.ac.uk/efo/EFO_0021848 GCST90237094 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase level in Chronic kidney disease with hypertension and no diabetes (7016_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041691 GCST90238446 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosome biogenesis protein TSR3 homolog level in Chronic kidney disease with hypertension and no diabetes (7018_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 18S rRNA aminocarboxypropyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044480 GCST90238447 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-7A level in Chronic kidney disease with hypertension and no diabetes (7019_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-7A in blood serum http://purl.obolibrary.org/obo/OBA_2040388 GCST90238448 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 5 level in Chronic kidney disease with hypertension and no diabetes (7020_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041026 GCST90238449 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase level in Chronic kidney disease with hypertension and no diabetes (7038_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMP-N-acetylneuraminate-poly-alpha-2,8-sialyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043684 GCST90238450 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 level in Chronic kidney disease with hypertension and no diabetes (7045_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BCL2/adenovirus E1B 19 kDa protein-interacting protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040814 GCST90238451 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C20orf173 level in Chronic kidney disease with hypertension and no diabetes (7046_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C20orf173 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044920 GCST90238452 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 19 level in Chronic kidney disease with hypertension and no diabetes (7048_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 19 in blood serum http://purl.obolibrary.org/obo/OBA_2040977 GCST90238453 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 23 level in Chronic kidney disease with hypertension and no diabetes (7049_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 23 in blood serum http://purl.obolibrary.org/obo/OBA_2040498 GCST90238454 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal growth regulator 1 level in Chronic kidney disease with hypertension and no diabetes (7050_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuronal growth regulator 1 measurement http://www.ebi.ac.uk/efo/EFO_0021932 GCST90238455 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 2 member D level in Chronic kidney disease with hypertension and no diabetes (7054_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 2 member D in blood serum http://purl.obolibrary.org/obo/OBA_2041045 GCST90238456 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 4F2 cell-surface antigen heavy chain level in Chronic kidney disease with hypertension and no diabetes (7056_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238457 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily A member 6 level in Chronic kidney disease with hypertension and no diabetes (7059_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily A member 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042198 GCST90238458 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ERO1-like protein alpha level in Chronic kidney disease with hypertension and no diabetes (7060_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ERO1-like protein alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041508 GCST90238459 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-associated membrane protein 8 level in Chronic kidney disease with hypertension and no diabetes (7064_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-associated membrane protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044079 GCST90238460 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein G6b level in Chronic kidney disease with hypertension and no diabetes (7065_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238461 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM209B level in Chronic kidney disease with hypertension and no diabetes (7066_199) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM209B in blood serum http://purl.obolibrary.org/obo/OBA_2044698 GCST90238462 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. t-SNARE domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (7069_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of t-SNARE domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044401 GCST90238463 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kell blood group glycoprotein level in Chronic kidney disease with hypertension and no diabetes (7070_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kell blood group glycoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2040344 GCST90238464 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase level in Chronic kidney disease with hypertension and no diabetes (7071_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase in blood serum http://purl.obolibrary.org/obo/OBA_2042276 GCST90238465 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C22orf15 level in Chronic kidney disease with hypertension and no diabetes (7073_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C22orf15 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044918 GCST90238466 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelin-converting enzyme-like 1 level in Chronic kidney disease with hypertension and no diabetes (7076_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endothelin-converting enzyme-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041405 GCST90238467 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6 level in Chronic kidney disease with hypertension and no diabetes (7082_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acetylgalactosaminyl-O-glycosyl-glycoprotein beta-1,3-N-acetylglucosaminyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2040753 GCST90238468 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrilin-4 level in Chronic kidney disease with hypertension and no diabetes (7083_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of matrilin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042306 GCST90238469 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Draxin level in Chronic kidney disease with hypertension and no diabetes (7084_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of draxin in blood serum http://purl.obolibrary.org/obo/OBA_2044466 GCST90238470 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Corneodesmosin level in Chronic kidney disease with hypertension and no diabetes (7085_81) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of corneodesmosin in blood serum http://purl.obolibrary.org/obo/OBA_2040974 GCST90238471 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-11 level in Chronic kidney disease with hypertension and no diabetes (7089_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-11 in blood serum http://purl.obolibrary.org/obo/OBA_2043749 GCST90238472 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (7090_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041659 GCST90238473 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase-like protein of the testis level in Chronic kidney disease with hypertension and no diabetes (7092_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein disulfide-isomerase-like protein of the testis in blood serum http://purl.obolibrary.org/obo/OBA_2042831 GCST90238474 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testis-specific chromodomain protein Y 1 level in Chronic kidney disease with hypertension and no diabetes (7097_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of testis-specific chromodomain protein Y 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044804 GCST90238475 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follistatin-related protein 5 level in Chronic kidney disease with hypertension and no diabetes (7099_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of follistatin-related protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041623 GCST90238476 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface antigen CD2 level in Chronic kidney disease with hypertension and no diabetes (7100_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD2 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040237 GCST90238477 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-binding protein 7 level in Chronic kidney disease with hypertension and no diabetes (7104_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-binding protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040867 GCST90238478 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CDK5 and ABL1 enzyme substrate 2 level in Chronic kidney disease with hypertension and no diabetes (7105_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CDK5 and ABL1 enzyme substrate 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040864 GCST90238479 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oocyte-secreted protein 2 level in Chronic kidney disease with hypertension and no diabetes (7106_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oocyte-secreted protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042917 GCST90238480 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small integral membrane protein 24 level in Chronic kidney disease with hypertension and no diabetes (7108_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small integral membrane protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2044821 GCST90238481 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GrpE protein homolog 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7113_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GrpE protein homolog 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041795 GCST90238482 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semenogelin-1 level in Chronic kidney disease with hypertension and no diabetes (7115_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of semenogelin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043438 GCST90238483 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteoclast-associated immunoglobulin-like receptor level in Chronic kidney disease with hypertension and no diabetes (7116_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of osteoclast-associated immunoglobulin-like receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042715 GCST90238484 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin I2 level in Chronic kidney disease with hypertension and no diabetes (7117_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin I2 in blood serum http://purl.obolibrary.org/obo/OBA_2043466 GCST90238485 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily DCC subclass member 3 level in Chronic kidney disease with hypertension and no diabetes (7118_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238486 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-7 level in Chronic kidney disease with hypertension and no diabetes (7121_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-7 in blood serum http://purl.obolibrary.org/obo/OBA_2043757 GCST90238487 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing G-protein coupled receptor 5 level in Chronic kidney disease with hypertension and no diabetes (7122_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing G-protein coupled receptor 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040311 GCST90238488 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L52, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7123_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L52, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042432 GCST90238489 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-21 level in Chronic kidney disease with hypertension and no diabetes (7124_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-21 in blood serum http://purl.obolibrary.org/obo/OBA_2040288 GCST90238490 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein A-II level in Chronic kidney disease with hypertension and no diabetes (7127_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of apolipoprotein A-II in blood serum http://purl.obolibrary.org/obo/OBA_2040622 GCST90238491 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. von Willebrand factor A domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (7128_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of von Willebrand factor A domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044584 GCST90238492 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte-associated immunoglobulin-like receptor 2 level in Chronic kidney disease with hypertension and no diabetes (7130_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte-associated immunoglobulin-like receptor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040346 GCST90238493 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin level in Chronic kidney disease with hypertension and no diabetes (7131_207) 466 African American individuals NA Illumina [14870897] (imputed) 1 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90238494 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cholesteryl ester transfer protein level in Chronic kidney disease with hypertension and no diabetes (7131_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 cholesteryl ester transfer protein measurement http://www.ebi.ac.uk/efo/EFO_0009133 GCST90238495 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin growth factor-like family member 3 level in Chronic kidney disease with hypertension and no diabetes (6961_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin growth factor-like family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044591 GCST90238421 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Placenta growth factor level in Chronic kidney disease with hypertension and no diabetes (3078_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 placenta growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010626 GCST90237232 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-associated protein-like 2 level in Chronic kidney disease with hypertension and no diabetes (6965_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of contactin-associated protein-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041075 GCST90238423 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-1B level in Chronic kidney disease with hypertension and no diabetes (6966_144) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-1B in blood serum http://purl.obolibrary.org/obo/OBA_2043712 GCST90238424 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2D ligand 2 level in Chronic kidney disease with hypertension and no diabetes (3082_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UL16-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044029 GCST90237235 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HLA class II histocompatibility antigen gamma chain level in Chronic kidney disease with hypertension and no diabetes (6974_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MHC class II histocompatibility antigen gamma chain in blood serum http://purl.obolibrary.org/obo/OBA_2040331 GCST90238426 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aurora kinase A level in Chronic kidney disease with hypertension and no diabetes (3091_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 aurora kinase A measurement http://www.ebi.ac.uk/efo/EFO_0020168 GCST90237237 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 1 level in Chronic kidney disease with hypertension and no diabetes (3115_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020574 GCST90237238 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diablo homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (3122_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 diablo homolog, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020323 GCST90237239 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor C level in Chronic kidney disease with hypertension and no diabetes (3132_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 vascular endothelial growth factor C measurement http://www.ebi.ac.uk/efo/EFO_0020848 GCST90237240 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD4 level in Chronic kidney disease with hypertension and no diabetes (3143_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 t-cell surface glycoprotein CD4 measurement http://www.ebi.ac.uk/efo/EFO_0020760 GCST90237241 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemoglobin subunit delta level in Chronic kidney disease with hypertension and no diabetes (6992_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hemoglobin subunit delta in blood serum http://purl.obolibrary.org/obo/OBA_2041840 GCST90238432 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5'-Nucleotidase level in Chronic kidney disease with hypertension and no diabetes (6993_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5'-nucleotidase in blood serum http://purl.obolibrary.org/obo/OBA_2040327 GCST90238433 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-2 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3151_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 soluble interleukin-2 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0007650 GCST90237243 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-26 level in Chronic kidney disease with hypertension and no diabetes (6997_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-26 in blood serum http://purl.obolibrary.org/obo/OBA_2043148 GCST90238435 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartyl/asparaginyl beta-hydroxylase level in Chronic kidney disease with hypertension and no diabetes (6998_106) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of aspartyl/asparaginyl beta-hydroxylase in blood serum http://purl.obolibrary.org/obo/OBA_2040705 GCST90238436 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myeloid cell surface antigen CD33 level in Chronic kidney disease with hypertension and no diabetes (3166_92) 466 African American individuals NA Illumina [14870897] (imputed) 1 myeloid cell surface antigen CD33 measurement http://www.ebi.ac.uk/efo/EFO_0008238 GCST90237245 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A disintegrin and metalloproteinase with thrombospondin motifs 5 level in Chronic kidney disease with hypertension and no diabetes (3168_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 5 measurement http://www.ebi.ac.uk/efo/EFO_0008326 GCST90237246 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trafficking protein particle complex subunit 4 level in Chronic kidney disease with hypertension and no diabetes (7007_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trafficking protein particle complex subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043920 GCST90238440 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein eva-1 homolog C level in Chronic kidney disease with hypertension and no diabetes (7008_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238441 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell differentiation antigen CD72 level in Chronic kidney disease with hypertension and no diabetes (7009_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD72 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040259 GCST90238442 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell differentiation antigen CD72 level in Chronic kidney disease with hypertension and no diabetes (7009_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD72 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040259 GCST90238443 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular non-inflammatory molecule 2 level in Chronic kidney disease with hypertension and no diabetes (7012_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pantetheine hydrolase VNN2 in blood serum http://purl.obolibrary.org/obo/OBA_2044105 GCST90238444 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily B member 5 level in Chronic kidney disease with hypertension and no diabetes (7015_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily B member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042201 GCST90238445 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acylethanolamine-hydrolyzing acid amidase level in Chronic kidney disease with hypertension and no diabetes (3173_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 N-acylethanolamine-hydrolyzing acid amidase measurement http://www.ebi.ac.uk/efo/EFO_0008240 GCST90237251 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A disintegrin and metalloproteinase with thrombospondin motifs 1 level in Chronic kidney disease with hypertension and no diabetes (3174_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 1 measurement http://www.ebi.ac.uk/efo/EFO_0021968 GCST90237252 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A disintegrin and metalloproteinase with thrombospondin motifs 13 level in Chronic kidney disease with hypertension and no diabetes (3175_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 a disintegrin and metalloproteinase with thrombospondin motifs 13 measurement http://www.ebi.ac.uk/efo/EFO_0008011 GCST90237253 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dipeptidyl peptidase 1 level in Chronic kidney disease with hypertension and no diabetes (3178_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 dipeptidyl peptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020325 GCST90237254 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysosomal protective protein level in Chronic kidney disease with hypertension and no diabetes (3179_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 lysosomal protective protein measurement http://www.ebi.ac.uk/efo/EFO_0008215 GCST90237255 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (7132_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q-like protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040848 GCST90238496 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bcl-2-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (7134_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 bcl-2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021928 GCST90238497 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemoglobin subunit epsilon level in Chronic kidney disease with hypertension and no diabetes (7136_107) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hemoglobin subunit epsilon in blood serum http://purl.obolibrary.org/obo/OBA_2044309 GCST90238498 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial peptide methionine sulfoxide reductase level in Chronic kidney disease with hypertension and no diabetes (7137_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptide methionine sulfoxide reductase in blood serum http://purl.obolibrary.org/obo/OBA_2042442 GCST90238499 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT and NTRK-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (7139_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLIT and NTRK-like protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043549 GCST90238500 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymotrypsin-like elastase family member 2A level in Chronic kidney disease with hypertension and no diabetes (7140_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chymotrypsin-like elastase family member 2A in blood serum http://purl.obolibrary.org/obo/OBA_2041460 GCST90238501 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B level in Chronic kidney disease with hypertension and no diabetes (7141_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B in blood serum http://purl.obolibrary.org/obo/OBA_2042360 GCST90238502 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase N catalytic chain level in Chronic kidney disease with hypertension and no diabetes (7142_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase N catalytic chain in blood serum http://purl.obolibrary.org/obo/OBA_2041121 GCST90238503 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase, isoform C level in Chronic kidney disease with hypertension and no diabetes (7143_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetyllactosaminide beta-1,6-N-acetylglucosaminyl-transferase in blood serum http://purl.obolibrary.org/obo/OBA_2041692 GCST90238504 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kazal-type serine protease inhibitor domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (7144_234) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Kazal-type serine protease inhibitor domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042084 GCST90238505 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inter-alpha-trypsin inhibitor heavy chain H3 level in Chronic kidney disease with hypertension and no diabetes (7145_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of inter-alpha-trypsin inhibitor heavy chain H3 in blood serum http://purl.obolibrary.org/obo/OBA_2042058 GCST90238506 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase A4 level in Chronic kidney disease with hypertension and no diabetes (7146_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein disulfide-isomerase A4 in blood serum http://purl.obolibrary.org/obo/OBA_2042828 GCST90238507 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase A4 level in Chronic kidney disease with hypertension and no diabetes (7146_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein disulfide-isomerase A4 in blood serum http://purl.obolibrary.org/obo/OBA_2042828 GCST90238508 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 8 level in Chronic kidney disease with hypertension and no diabetes (7147_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WAP four-disulfide core domain protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044548 GCST90238509 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM173A level in Chronic kidney disease with hypertension and no diabetes (7148_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adenine nucleotide translocase lysine N-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044742 GCST90238510 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatitis A virus cellular receptor 2 level in Chronic kidney disease with hypertension and no diabetes (7152_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90238511 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neugrin level in Chronic kidney disease with hypertension and no diabetes (7153_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neugrin in blood serum http://purl.obolibrary.org/obo/OBA_2042577 GCST90238512 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein LEG1 homolog level in Chronic kidney disease with hypertension and no diabetes (7154_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein LEG1 homolog in blood serum http://purl.obolibrary.org/obo/OBA_2044833 GCST90238513 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-(1,3)-fucosyltransferase 10 level in Chronic kidney disease with hypertension and no diabetes (7156_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of alpha-(1,3)-fucosyltransferase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041632 GCST90238514 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin alpha-4 level in Chronic kidney disease with hypertension and no diabetes (7157_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin alpha-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042785 GCST90238515 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDH/6PGL endoplasmic bifunctional protein level in Chronic kidney disease with hypertension and no diabetes (7161_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of GDH/6PGL endoplasmic bifunctional protein in blood serum http://purl.obolibrary.org/obo/OBA_2041829 GCST90238516 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 132C level in Chronic kidney disease with hypertension and no diabetes (7173_141) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238517 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 6 level in Chronic kidney disease with hypertension and no diabetes (14088_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020478 GCST90234180 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Differentially expressed in FDCP 6 homolog level in Chronic kidney disease with hypertension and no diabetes (14090_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of differentially expressed in FDCP 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041264 GCST90234181 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonyl reductase [NADPH] 3 level in Chronic kidney disease with hypertension and no diabetes (14091_42) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of carbonyl reductase [NADPH] 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040917 GCST90234182 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 E1 level in Chronic kidney disease with hypertension and no diabetes (14326_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 E1 in blood serum http://purl.obolibrary.org/obo/OBA_2043993 GCST90234258 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Death-inducer obliterator 1 level in Chronic kidney disease with hypertension and no diabetes (14329_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of death-inducer obliterator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041302 GCST90234259 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynein light chain Tctex-type 1 level in Chronic kidney disease with hypertension and no diabetes (14331_262) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynein light chain Tctex-type 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041395 GCST90234260 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Ral-A level in Chronic kidney disease with hypertension and no diabetes (14332_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Ral-A in blood serum http://purl.obolibrary.org/obo/OBA_2043186 GCST90234261 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Recoverin level in Chronic kidney disease with hypertension and no diabetes (14334_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of recoverin in blood serum http://purl.obolibrary.org/obo/OBA_2043222 GCST90234262 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trafficking protein particle complex subunit 3 level in Chronic kidney disease with hypertension and no diabetes (14337_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trafficking protein particle complex subunit 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043919 GCST90234263 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM69C level in Chronic kidney disease with hypertension and no diabetes (14341_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of divergent protein kinase domain 1C in blood serum http://purl.obolibrary.org/obo/OBA_2044546 GCST90234264 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM210A level in Chronic kidney disease with hypertension and no diabetes (14593_152) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein FAM210A in blood serum http://purl.obolibrary.org/obo/OBA_2044718 GCST90234265 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-6C, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (14597_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-6C in blood serum http://purl.obolibrary.org/obo/OBA_2043436 GCST90234266 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stabilin-1 level in Chronic kidney disease with hypertension and no diabetes (14599_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stabilin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043686 GCST90234267 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein KIAA0040 level in Chronic kidney disease with hypertension and no diabetes (14603_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein KIAA0040 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044903 GCST90234268 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noncompact myelin-associated protein level in Chronic kidney disease with hypertension and no diabetes (14614_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of noncompact myelin-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2044518 GCST90234269 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin-associated protein 2-4 level in Chronic kidney disease with hypertension and no diabetes (14615_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin-associated protein 2-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042149 GCST90234270 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 382 level in Chronic kidney disease with hypertension and no diabetes (14616_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 382 in blood serum http://purl.obolibrary.org/obo/OBA_2044203 GCST90234271 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicular, overexpressed in cancer, prosurvival protein 1 level in Chronic kidney disease with hypertension and no diabetes (14618_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicular, overexpressed in cancer, prosurvival protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041408 GCST90234272 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 526 level in Chronic kidney disease with hypertension and no diabetes (14619_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 526 in blood serum http://purl.obolibrary.org/obo/OBA_2044207 GCST90234273 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small ubiquitin-related modifier 3 level in Chronic kidney disease with hypertension and no diabetes (14623_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 small ubiquitin-related modifier 3 measurement http://www.ebi.ac.uk/efo/EFO_0022025 GCST90234274 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional repressor CTCF level in Chronic kidney disease with hypertension and no diabetes (14624_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional repressor CTCF in blood serum http://purl.obolibrary.org/obo/OBA_2041182 GCST90234275 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin subfamily 3 member A2 level in Chronic kidney disease with hypertension and no diabetes (21433_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of butyrophilin subfamily 3 member A2 in blood serum http://purl.obolibrary.org/obo/OBA_2044673 GCST90235715 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase SRPK2 level in Chronic kidney disease with hypertension and no diabetes (21435_143) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SRSF protein kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043659 GCST90235716 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine protease ATG4A level in Chronic kidney disease with hypertension and no diabetes (21436_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine protease ATG4A in blood serum http://purl.obolibrary.org/obo/OBA_2040718 GCST90235717 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methylated-DNA--protein-cysteine methyltransferase level in Chronic kidney disease with hypertension and no diabetes (21437_77) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of methylated-DNA--protein-cysteine methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042363 GCST90235718 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hematopoietic lineage cell-specific protein level in Chronic kidney disease with hypertension and no diabetes (21439_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hematopoietic lineage cell-specific protein in blood serum http://purl.obolibrary.org/obo/OBA_2041845 GCST90235719 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADAM 8 level in Chronic kidney disease with hypertension and no diabetes (21440_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040254 GCST90235720 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. gp75 level in Chronic kidney disease with hypertension and no diabetes (21441_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5,6-dihydroxyindole-2-carboxylic acid oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2043976 GCST90235721 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A7 level in Chronic kidney disease with hypertension and no diabetes (14203_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A7 in blood serum http://purl.obolibrary.org/obo/OBA_2040602 GCST90234233 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein J2 level in Chronic kidney disease with hypertension and no diabetes (14204_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein J2 in blood serum http://purl.obolibrary.org/obo/OBA_2041607 GCST90234234 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein HEXIM2 level in Chronic kidney disease with hypertension and no diabetes (14205_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein HEXIM2 in blood serum http://purl.obolibrary.org/obo/OBA_2041867 GCST90234235 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 precursor protein-binding family B member 1 level in Chronic kidney disease with hypertension and no diabetes (14206_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234236 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoid-binding protein 7 level in Chronic kidney disease with hypertension and no diabetes (14208_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinoid-binding protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043214 GCST90234237 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-methylmethionine--homocysteine S-methyltransferase BHMT2 level in Chronic kidney disease with hypertension and no diabetes (14226_120) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of betaine--homocysteine S-methyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040797 GCST90234238 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin light chain 6B level in Chronic kidney disease with hypertension and no diabetes (14227_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin light chain 6B in blood serum http://purl.obolibrary.org/obo/OBA_2042482 GCST90234239 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenylyltransferase and sulfurtransferase MOCS3 level in Chronic kidney disease with hypertension and no diabetes (14229_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adenylyltransferase and sulfurtransferase MOCS3 in blood serum http://purl.obolibrary.org/obo/OBA_2042399 GCST90234240 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (14237_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90234241 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Docking protein 2 level in Chronic kidney disease with hypertension and no diabetes (14246_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of docking protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041344 GCST90234242 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable E3 ubiquitin-protein ligase MID2 level in Chronic kidney disease with hypertension and no diabetes (14249_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of midline-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042368 GCST90234243 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bleomycin hydrolase level in Chronic kidney disease with hypertension and no diabetes (14250_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bleomycin hydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2040803 GCST90234244 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 4 level in Chronic kidney disease with hypertension and no diabetes (14254_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein phosphatase non-receptor type 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043102 GCST90234245 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroepithelial cell-transforming gene 1 protein level in Chronic kidney disease with hypertension and no diabetes (14260_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroepithelial cell-transforming gene 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042561 GCST90234246 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfiredoxin-1 level in Chronic kidney disease with hypertension and no diabetes (14268_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfiredoxin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043661 GCST90234247 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-6B level in Chronic kidney disease with hypertension and no diabetes (14271_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-6B in blood serum http://purl.obolibrary.org/obo/OBA_2043170 GCST90234248 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolyl endopeptidase level in Chronic kidney disease with hypertension and no diabetes (14273_19) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prolyl endopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2043022 GCST90234249 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-14 level in Chronic kidney disease with hypertension and no diabetes (14283_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-14 in blood serum http://purl.obolibrary.org/obo/OBA_2043140 GCST90234250 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear factor of activated T-cells, cytoplasmic 1 level in Chronic kidney disease with hypertension and no diabetes (14286_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear factor of activated T-cells, cytoplasmic 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040415 GCST90234251 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-5C level in Chronic kidney disease with hypertension and no diabetes (14287_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-5C in blood serum http://purl.obolibrary.org/obo/OBA_2043168 GCST90234252 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (14291_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040533 GCST90234253 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein H level in Chronic kidney disease with hypertension and no diabetes (14309_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein H in blood serum http://purl.obolibrary.org/obo/OBA_2041907 GCST90234254 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase-like 2 level in Chronic kidney disease with hypertension and no diabetes (14314_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RING-type E3 ubiquitin-protein ligase PPIL2 in blood serum http://purl.obolibrary.org/obo/OBA_2042989 GCST90234255 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein sorting-associated protein 29 level in Chronic kidney disease with hypertension and no diabetes (14318_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of vacuolar protein sorting-associated protein 29 in blood serum http://purl.obolibrary.org/obo/OBA_2044110 GCST90234256 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Structural maintenance of chromosomes protein 3 level in Chronic kidney disease with hypertension and no diabetes (14324_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of structural maintenance of chromosomes protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043554 GCST90234257 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation factor Xa level in Chronic kidney disease with hypertension and no diabetes (3077_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 coagulation factor XA measurement http://www.ebi.ac.uk/efo/EFO_0020266 GCST90237231 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HLA class II histocompatibility antigen, DR beta 3 chain level in Chronic kidney disease with hypertension and no diabetes (6962_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MHC class II histocompatibility antigen beta chain DRB3 in blood serum http://purl.obolibrary.org/obo/OBA_2040365 GCST90238422 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoic acid receptor responder protein 2 level in Chronic kidney disease with hypertension and no diabetes (3079_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 retinoic acid receptor responder protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008274 GCST90237233 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2D ligand 1 level in Chronic kidney disease with hypertension and no diabetes (3081_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UL16-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044028 GCST90237234 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 5 level in Chronic kidney disease with hypertension and no diabetes (6969_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WAP four-disulfide core domain protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044134 GCST90238425 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 27 level in Chronic kidney disease with hypertension and no diabetes (3083_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 27 measurement http://www.ebi.ac.uk/efo/EFO_0020812 GCST90237236 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SNARE-associated protein Snapin level in Chronic kidney disease with hypertension and no diabetes (6975_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SNARE-associated protein Snapin in blood serum http://purl.obolibrary.org/obo/OBA_2043565 GCST90238427 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily member 8 level in Chronic kidney disease with hypertension and no diabetes (6984_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin superfamily member 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040240 GCST90238428 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan sulfate glucosamine 3-O-sulfotransferase 3B1 level in Chronic kidney disease with hypertension and no diabetes (6986_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heparan sulfate glucosamine 3-O-sulfotransferase 3B1 in blood serum http://purl.obolibrary.org/obo/OBA_2041932 GCST90238429 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal cell-derived factor 2-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (6990_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stromal cell-derived factor 2-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043414 GCST90238430 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-(1,3)-fucosyltransferase 9 level in Chronic kidney disease with hypertension and no diabetes (6991_24) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9 in blood serum http://purl.obolibrary.org/obo/OBA_2044485 GCST90238431 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gro-beta level in Chronic kidney disease with hypertension and no diabetes (3148_49) 466 African American individuals NA Illumina [14870897] (imputed) 7 level of C-X-C motif chemokine 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041207 GCST90237242 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C3orf18 level in Chronic kidney disease with hypertension and no diabetes (6994_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C3orf18 in blood serum http://purl.obolibrary.org/obo/OBA_2044879 GCST90238434 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 1B level in Chronic kidney disease with hypertension and no diabetes (3152_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90237244 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix-remodeling-associated protein 8 level in Chronic kidney disease with hypertension and no diabetes (7002_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238437 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 10 level in Chronic kidney disease with hypertension and no diabetes (7003_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041660 GCST90238438 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(XXV) chain level in Chronic kidney disease with hypertension and no diabetes (7006_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(XXV) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041085 GCST90238439 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-L-iduronidase level in Chronic kidney disease with hypertension and no diabetes (3169_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-L-iduronidase measurement http://www.ebi.ac.uk/efo/EFO_0020139 GCST90237247 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionine aminopeptidase 2 level in Chronic kidney disease with hypertension and no diabetes (3170_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 methionine aminopeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008232 GCST90237248 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 protein level in Chronic kidney disease with hypertension and no diabetes (3171_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 amyloid beta A4 protein measurement http://www.ebi.ac.uk/efo/EFO_0020145 GCST90237249 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arylsulfatase B level in Chronic kidney disease with hypertension and no diabetes (3172_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 arylsulfatase B measurement http://www.ebi.ac.uk/efo/EFO_0008030 GCST90237250 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fms-related tyrosine kinase 3 ligand level in Chronic kidney disease with hypertension and no diabetes (14093_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 obsolete_Fms-related tyrosine kinase 3 ligand measurement http://www.ebi.ac.uk/efo/EFO_0010594 GCST90234183 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparin-binding EGF-like growth factor level in Chronic kidney disease with hypertension and no diabetes (14094_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 heparin-binding egf-like growth factor measurement http://www.ebi.ac.uk/efo/EFO_0020438 GCST90234184 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 15 level in Chronic kidney disease with hypertension and no diabetes (14097_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90234185 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (14098_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cysteine--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2040901 GCST90234186 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-4 level in Chronic kidney disease with hypertension and no diabetes (14099_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit alpha type-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043064 GCST90234187 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ciliary neurotrophic factor receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (14101_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 ciliary neurotrophic factor receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020261 GCST90234188 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulysin level in Chronic kidney disease with hypertension and no diabetes (14102_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 granulysin measurement http://www.ebi.ac.uk/efo/EFO_0008144 GCST90234189 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptase gamma level in Chronic kidney disease with hypertension and no diabetes (14103_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 tryptase gamma measurement http://www.ebi.ac.uk/efo/EFO_0020792 GCST90234190 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TLR4 interactor with leucine rich repeats level in Chronic kidney disease with hypertension and no diabetes (14104_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234191 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallistatin level in Chronic kidney disease with hypertension and no diabetes (14105_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90234192 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rap1 GTPase-GDP dissociation stimulator 1 level in Chronic kidney disease with hypertension and no diabetes (14106_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rap1 GTPase-GDP dissociation stimulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043194 GCST90234193 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5-formyltetrahydrofolate cyclo-ligase level in Chronic kidney disease with hypertension and no diabetes (14107_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 5-formyltetrahydrofolate cyclo-ligase MTHFS in blood serum http://purl.obolibrary.org/obo/OBA_2042450 GCST90234194 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming growth factor beta-1 level in Chronic kidney disease with hypertension and no diabetes (14108_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 transforming growth factor beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020780 GCST90234195 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 15 level in Chronic kidney disease with hypertension and no diabetes (14109_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90234196 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPARC level in Chronic kidney disease with hypertension and no diabetes (14110_200) 466 African American individuals NA Illumina [14870897] (imputed) 0 SPARC measurement http://www.ebi.ac.uk/efo/EFO_0020748 GCST90234197 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin-2 level in Chronic kidney disease with hypertension and no diabetes (14111_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 thrombospondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008299 GCST90234198 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 19L level in Chronic kidney disease with hypertension and no diabetes (14112_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90234199 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PILR alpha-associated neural protein level in Chronic kidney disease with hypertension and no diabetes (14114_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 PILR alpha-associated neural protein measurement http://www.ebi.ac.uk/efo/EFO_0021941 GCST90234200 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adrenomedullin level in Chronic kidney disease with hypertension and no diabetes (14115_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 adrenomedullin measurement http://www.ebi.ac.uk/efo/EFO_0010909 GCST90234201 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A4 level in Chronic kidney disease with hypertension and no diabetes (14116_129) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein S100-A4 measurement http://www.ebi.ac.uk/efo/EFO_0021893 GCST90234202 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF43 level in Chronic kidney disease with hypertension and no diabetes (14120_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 e3 ubiquitin-protein ligase RNF43 measurement http://www.ebi.ac.uk/efo/EFO_0021886 GCST90234203 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 10D level in Chronic kidney disease with hypertension and no diabetes (14121_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 10D measurement http://www.ebi.ac.uk/efo/EFO_0021942 GCST90234204 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-type immunoglobulin domain-containing suppressor of T-cell activation level in Chronic kidney disease with hypertension and no diabetes (14123_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234205 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A2 level in Chronic kidney disease with hypertension and no diabetes (14124_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A2 measurement http://www.ebi.ac.uk/efo/EFO_0021944 GCST90234206 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein M level in Chronic kidney disease with hypertension and no diabetes (14125_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 apolipoprotein M measurement http://www.ebi.ac.uk/efo/EFO_0021945 GCST90234207 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon beta level in Chronic kidney disease with hypertension and no diabetes (14127_240) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon beta 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041983 GCST90234208 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-10 level in Chronic kidney disease with hypertension and no diabetes (14128_121) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon alpha-10 measurement http://www.ebi.ac.uk/efo/EFO_0021946 GCST90234209 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-7 level in Chronic kidney disease with hypertension and no diabetes (14129_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon alpha-7 measurement http://www.ebi.ac.uk/efo/EFO_0021947 GCST90234210 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-B2 level in Chronic kidney disease with hypertension and no diabetes (14131_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234211 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HERV-H LTR-associating protein 2 level in Chronic kidney disease with hypertension and no diabetes (14132_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 HERV-H LTR-associating protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021948 GCST90234212 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor type 2 level in Chronic kidney disease with hypertension and no diabetes (14133_93) 466 African American individuals NA Illumina [14870897] (imputed) 1 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90234213 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amphoterin-induced protein 2 level in Chronic kidney disease with hypertension and no diabetes (14134_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 amphoterin-induced protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021949 GCST90234214 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Relaxin receptor 1 level in Chronic kidney disease with hypertension and no diabetes (14135_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 relaxin receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021950 GCST90234215 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C1q receptor level in Chronic kidney disease with hypertension and no diabetes (14136_234) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement component C1q receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040369 GCST90234216 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuregulin-4 level in Chronic kidney disease with hypertension and no diabetes (14139_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuregulin-4 measurement http://www.ebi.ac.uk/efo/EFO_0021951 GCST90234217 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H2B type 2-E level in Chronic kidney disease with hypertension and no diabetes (14143_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone H2B type 2-E measurement http://www.ebi.ac.uk/efo/EFO_0021952 GCST90234218 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H2A type 3 level in Chronic kidney disease with hypertension and no diabetes (14144_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone H2A type 3 measurement http://www.ebi.ac.uk/efo/EFO_0021953 GCST90234219 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H3.1 level in Chronic kidney disease with hypertension and no diabetes (14146_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone H3.1 measurement http://www.ebi.ac.uk/efo/EFO_0021954 GCST90234220 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like protein ISG15 level in Chronic kidney disease with hypertension and no diabetes (14148_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin-like protein ISG15 measurement http://www.ebi.ac.uk/efo/EFO_0021875 GCST90234221 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-36 beta level in Chronic kidney disease with hypertension and no diabetes (14149_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-36 beta measurement http://www.ebi.ac.uk/efo/EFO_0021955 GCST90234222 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-36 alpha level in Chronic kidney disease with hypertension and no diabetes (14150_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 interleukin-36 alpha measurement http://www.ebi.ac.uk/efo/EFO_0021851 GCST90234223 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like protein ISG15 level in Chronic kidney disease with hypertension and no diabetes (14151_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin-like protein ISG15 measurement http://www.ebi.ac.uk/efo/EFO_0021875 GCST90234224 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A3 level in Chronic kidney disease with hypertension and no diabetes (14153_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A3 measurement http://www.ebi.ac.uk/efo/EFO_0021956 GCST90234225 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein beta/alpha level in Chronic kidney disease with hypertension and no diabetes (14156_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 14-3-3 protein beta/alpha measurement http://www.ebi.ac.uk/efo/EFO_0021957 GCST90234226 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein epsilon level in Chronic kidney disease with hypertension and no diabetes (14157_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 14-3-3 protein epsilon measurement http://www.ebi.ac.uk/efo/EFO_0021958 GCST90234227 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SCP2 sterol-binding domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (14175_78) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of SCP2 sterol-binding domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044878 GCST90234228 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase inhibitor 3 level in Chronic kidney disease with hypertension and no diabetes (14178_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase inhibitor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040973 GCST90234229 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase rififylin level in Chronic kidney disease with hypertension and no diabetes (14186_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase rififylin in blood serum http://purl.obolibrary.org/obo/OBA_2043245 GCST90234230 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosducin-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (14192_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosducin-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042817 GCST90234231 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PR domain zinc finger protein 1 level in Chronic kidney disease with hypertension and no diabetes (14197_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PR domain zinc finger protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040332 GCST90234232 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleolar protein of 40 kDa level in Chronic kidney disease with hypertension and no diabetes (21811_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of zinc finger CCHC domain-containing protein 17 in blood serum http://purl.obolibrary.org/obo/OBA_2044176 GCST90235882 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A level in Chronic kidney disease with hypertension and no diabetes (21813_171) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A in blood serum http://purl.obolibrary.org/obo/OBA_2042362 GCST90235883 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methylmalonic aciduria and homocystinuria type D protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (21814_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cobalamin trafficking protein CblD in blood serum http://purl.obolibrary.org/obo/OBA_2042385 GCST90235884 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MOB kinase activator 3B level in Chronic kidney disease with hypertension and no diabetes (21815_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MOB kinase activator 3B in blood serum http://purl.obolibrary.org/obo/OBA_2042396 GCST90235885 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Negative elongation factor E level in Chronic kidney disease with hypertension and no diabetes (21819_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of negative elongation factor E in blood serum http://purl.obolibrary.org/obo/OBA_2043223 GCST90235886 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1G level in Chronic kidney disease with hypertension and no diabetes (21823_5) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of protein phosphatase 1G in blood serum http://purl.obolibrary.org/obo/OBA_2042995 GCST90235887 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-related GTP-binding protein RhoQ level in Chronic kidney disease with hypertension and no diabetes (21827_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-related GTP-binding protein RhoQ in blood serum http://purl.obolibrary.org/obo/OBA_2043268 GCST90235888 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribophorin II level in Chronic kidney disease with hypertension and no diabetes (21828_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043325 GCST90235889 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S12 level in Chronic kidney disease with hypertension and no diabetes (21829_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 40S ribosomal protein S12 in blood serum http://purl.obolibrary.org/obo/OBA_2043330 GCST90235890 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C4b level in Chronic kidney disease with hypertension and no diabetes (2182_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement C4b measurement http://www.ebi.ac.uk/efo/EFO_0008092 GCST90235891 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Squamous cell carcinoma antigen 1 level in Chronic kidney disease with hypertension and no diabetes (21832_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin B3 in blood serum http://purl.obolibrary.org/obo/OBA_2043460 GCST90235892 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. silent mating type information regulation 2 homolog level in Chronic kidney disease with hypertension and no diabetes (21833_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NAD-dependent protein deacylase sirtuin-6 in blood serum http://purl.obolibrary.org/obo/OBA_2043515 GCST90235893 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Somatostatin receptor type 1 level in Chronic kidney disease with hypertension and no diabetes (21836_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of somatostatin receptor type 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040316 GCST90235894 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translocon-associated protein subunit beta level in Chronic kidney disease with hypertension and no diabetes (21837_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of translocon-associated protein subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2043667 GCST90235895 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. POU domain class 2-associating factor 1 level in Chronic kidney disease with hypertension and no diabetes (21839_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of POU domain class 2-associating factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042975 GCST90235896 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 R2 level in Chronic kidney disease with hypertension and no diabetes (21848_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 R2 in blood serum http://purl.obolibrary.org/obo/OBA_2044002 GCST90235897 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquilin-3 level in Chronic kidney disease with hypertension and no diabetes (21849_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquilin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2044013 GCST90235898 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ketohexokinase level in Chronic kidney disease with hypertension and no diabetes (21856_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ketohexokinase in blood serum http://purl.obolibrary.org/obo/OBA_2042094 GCST90235899 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein subunit beta-2-like 1 level in Chronic kidney disease with hypertension and no diabetes (21857_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor of activated protein C kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041750 GCST90235900 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase SIAH1 level in Chronic kidney disease with hypertension and no diabetes (21858_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase SIAH1 in blood serum http://purl.obolibrary.org/obo/OBA_2043506 GCST90235901 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-10 level in Chronic kidney disease with hypertension and no diabetes (21861_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of proteasome subunit beta type-10 in blood serum http://purl.obolibrary.org/obo/OBA_2043068 GCST90235902 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM and SH3 domain protein 1 level in Chronic kidney disease with hypertension and no diabetes (21862_145) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LIM and SH3 domain protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042165 GCST90235903 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic Fe-S cluster assembly factor NUBP2 level in Chronic kidney disease with hypertension and no diabetes (21863_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cytosolic Fe-S cluster assembly factor NUBP2 in blood serum http://purl.obolibrary.org/obo/OBA_2042659 GCST90235904 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AN1-type zinc finger protein 3 level in Chronic kidney disease with hypertension and no diabetes (21875_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AN1-type zinc finger protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044179 GCST90235905 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PRKCA-binding protein level in Chronic kidney disease with hypertension and no diabetes (21876_266) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PRKCA-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2042885 GCST90235906 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A2 level in Chronic kidney disease with hypertension and no diabetes (10801_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A2 measurement http://www.ebi.ac.uk/efo/EFO_0021944 GCST90232990 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (10803_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90232991 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell lectin-like receptor subfamily B member 1 level in Chronic kidney disease with hypertension and no diabetes (10809_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of killer cell lectin-like receptor subfamily B member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044226 GCST90232992 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD1a level in Chronic kidney disease with hypertension and no diabetes (10814_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-cell surface glycoprotein CD1a in blood serum http://purl.obolibrary.org/obo/OBA_2040367 GCST90232993 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intracellular hyaluronan-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (10815_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of intracellular hyaluronan-binding protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041831 GCST90232994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sphingomyelin phosphodiesterase level in Chronic kidney disease with hypertension and no diabetes (10818_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sphingomyelin phosphodiesterase in blood serum http://purl.obolibrary.org/obo/OBA_2043558 GCST90232995 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibulin-1 level in Chronic kidney disease with hypertension and no diabetes (10819_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibulin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041552 GCST90232996 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and immunoglobulin domain-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (10825_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of V-set and immunoglobulin domain-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044378 GCST90232997 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 level in Chronic kidney disease with hypertension and no diabetes (10827_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044497 GCST90232998 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EF-hand calcium-binding domain-containing protein 14 level in Chronic kidney disease with hypertension and no diabetes (10830_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232999 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4-galactosyltransferase 6 level in Chronic kidney disease with hypertension and no diabetes (10832_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,4-galactosyltransferase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040760 GCST90233000 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hedgehog-interacting protein level in Chronic kidney disease with hypertension and no diabetes (10833_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hedgehog-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2041872 GCST90233001 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,4-N-acetylglucosaminyltransferase level in Chronic kidney disease with hypertension and no diabetes (10835_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,4-N-acetylglucosaminyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2040452 GCST90233002 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 level in Chronic kidney disease with hypertension and no diabetes (10842_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041693 GCST90233003 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 15 level in Chronic kidney disease with hypertension and no diabetes (10847_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sialic acid-binding Ig-like lectin 15 in blood serum http://purl.obolibrary.org/obo/OBA_2043508 GCST90233004 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (10848_137) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of butyrophilin-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040836 GCST90233005 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-27 subunit beta level in Chronic kidney disease with hypertension and no diabetes (10851_77) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-27 subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040289 GCST90233006 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein D-like level in Chronic kidney disease with hypertension and no diabetes (10852_114) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein D-like in blood serum http://purl.obolibrary.org/obo/OBA_2041910 GCST90233007 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 level in Chronic kidney disease with hypertension and no diabetes (10854_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041693 GCST90233008 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin-B2 level in Chronic kidney disease with hypertension and no diabetes (10855_55) 466 African American individuals NA Illumina [14870897] (imputed) 1 plexin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0021867 GCST90233009 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 4 regulatory subunit 3A level in Chronic kidney disease with hypertension and no diabetes (10866_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein phosphatase 4 regulatory subunit 3A in blood serum http://purl.obolibrary.org/obo/OBA_2043555 GCST90233010 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spastin level in Chronic kidney disease with hypertension and no diabetes (10870_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233011 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRCA1-associated ATM activator 1 level in Chronic kidney disease with hypertension and no diabetes (10876_300) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRCA1-associated ATM activator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044693 GCST90233012 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM163B level in Chronic kidney disease with hypertension and no diabetes (10880_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM163B in blood serum http://purl.obolibrary.org/obo/OBA_2044679 GCST90233013 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmocollin-1 level in Chronic kidney disease with hypertension and no diabetes (10882_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of desmocollin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041365 GCST90233014 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiotensin-converting enzyme level in Chronic kidney disease with hypertension and no diabetes (10714_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 angiotensin converting enzyme activity measurement http://www.ebi.ac.uk/efo/EFO_0004463 GCST90232965 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S proteasome non-ATPase regulatory subunit 5 level in Chronic kidney disease with hypertension and no diabetes (10716_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 26S proteasome non-ATPase regulatory subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043077 GCST90232966 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (10721_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90232967 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase SYK level in Chronic kidney disease with hypertension and no diabetes (10722_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232968 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan sulfate glucosamine 3-O-sulfotransferase 5 level in Chronic kidney disease with hypertension and no diabetes (10731_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of heparan sulfate glucosamine 3-O-sulfotransferase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041934 GCST90232969 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte elastase inhibitor level in Chronic kidney disease with hypertension and no diabetes (10737_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte elastase inhibitor in blood serum http://purl.obolibrary.org/obo/OBA_2043458 GCST90232970 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibulin-5 level in Chronic kidney disease with hypertension and no diabetes (10738_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibulin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2041553 GCST90232971 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage colony-stimulating factor 1 level in Chronic kidney disease with hypertension and no diabetes (10741_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage colony-stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020546 GCST90232972 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT and NTRK-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (10743_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 SLIT and NTRK-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021974 GCST90232973 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dickkopf-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (10746_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90232974 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin beta-2 level in Chronic kidney disease with hypertension and no diabetes (10748_216) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042791 GCST90232975 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (10749_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90232976 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromodomain Y-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (10752_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of chromodomain Y-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044268 GCST90232977 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 7 level in Chronic kidney disease with hypertension and no diabetes (10753_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040503 GCST90232978 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prokineticin-2 level in Chronic kidney disease with hypertension and no diabetes (10754_113) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prokineticin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043035 GCST90232979 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urocortin-3 level in Chronic kidney disease with hypertension and no diabetes (10756_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of urocortin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2044019 GCST90232980 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratocan level in Chronic kidney disease with hypertension and no diabetes (10758_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratocan in blood serum http://purl.obolibrary.org/obo/OBA_2042092 GCST90232981 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate receptor 4 level in Chronic kidney disease with hypertension and no diabetes (10760_107) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of glutamate receptor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041788 GCST90232982 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane emp24 domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (10761_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane emp24 domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043868 GCST90232983 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell lectin-like receptor subfamily G member 2 level in Chronic kidney disease with hypertension and no diabetes (10762_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232984 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G-protein coupled receptor 64 level in Chronic kidney disease with hypertension and no diabetes (10767_52) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of adhesion G-protein coupled receptor G2 in blood serum http://purl.obolibrary.org/obo/OBA_2041776 GCST90232985 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chondroitin sulfate N-acetylgalactosaminyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (10772_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chondroitin sulfate N-acetylgalactosaminyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041167 GCST90232986 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-3D level in Chronic kidney disease with hypertension and no diabetes (10780_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-3D in blood serum http://purl.obolibrary.org/obo/OBA_2043161 GCST90232987 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 4 member G level in Chronic kidney disease with hypertension and no diabetes (10781_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 4 member G in blood serum http://purl.obolibrary.org/obo/OBA_2044270 GCST90232988 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin H1 level in Chronic kidney disease with hypertension and no diabetes (10800_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin H1 in blood serum http://purl.obolibrary.org/obo/OBA_2043465 GCST90232989 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-2-HS-glycoprotein level in Chronic kidney disease with hypertension and no diabetes (10966_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90233040 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolactin level in Chronic kidney disease with hypertension and no diabetes (10967_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 prolactin measurement http://www.ebi.ac.uk/efo/EFO_0007003 GCST90233041 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ecto-ADP-ribosyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (10970_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ecto-ADP-ribosyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040394 GCST90233042 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 7 level in Chronic kidney disease with hypertension and no diabetes (10974_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine protease inhibitor Kazal-type 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043635 GCST90233043 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mucin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (10975_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mucin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042460 GCST90233044 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mucin-1 level in Chronic kidney disease with hypertension and no diabetes (10976_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90233045 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Unique cartilage matrix-associated protein level in Chronic kidney disease with hypertension and no diabetes (10977_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of unique cartilage matrix-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2044018 GCST90233046 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth hormone variant level in Chronic kidney disease with hypertension and no diabetes (10978_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth hormone variant in blood serum http://purl.obolibrary.org/obo/OBA_2041714 GCST90233047 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acetylcholinesterase level in Chronic kidney disease with hypertension and no diabetes (10980_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of acetylcholinesterase in blood serum http://purl.obolibrary.org/obo/OBA_2040477 GCST90233048 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pro-neuregulin-3, membrane-bound isoform level in Chronic kidney disease with hypertension and no diabetes (10981_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pro-neuregulin-3, membrane-bound isoform in blood serum http://purl.obolibrary.org/obo/OBA_2042638 GCST90233049 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat serine/threonine-protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (10990_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 leucine-rich repeat serine/threonine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0021876 GCST90233050 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteocalcin level in Chronic kidney disease with hypertension and no diabetes (11067_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90233051 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-5 level in Chronic kidney disease with hypertension and no diabetes (11071_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2040292 GCST90233052 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (11081_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2041770 GCST90233053 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-enolase level in Chronic kidney disease with hypertension and no diabetes (11083_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 gamma-enolase measurement http://www.ebi.ac.uk/efo/EFO_0021845 GCST90233054 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin A level in Chronic kidney disease with hypertension and no diabetes (11089_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 serum IgA measurement http://www.ebi.ac.uk/efo/EFO_0004912 GCST90233055 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-10 level in Chronic kidney disease with hypertension and no diabetes (11094_104) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-10 measurement http://www.ebi.ac.uk/efo/EFO_0021918 GCST90233056 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HemK methyltransferase family member 2 level in Chronic kidney disease with hypertension and no diabetes (11096_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 hemK methyltransferase family member 2 measurement http://www.ebi.ac.uk/efo/EFO_0021891 GCST90233057 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor activity-modifying protein 3 level in Chronic kidney disease with hypertension and no diabetes (15437_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor activity-modifying protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043189 GCST90234372 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-related GTP-binding protein RhoE level in Chronic kidney disease with hypertension and no diabetes (15439_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-related GTP-binding protein RhoE in blood serum http://purl.obolibrary.org/obo/OBA_2043287 GCST90234373 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroendocrine convertase 2 level in Chronic kidney disease with hypertension and no diabetes (15440_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroendocrine convertase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042807 GCST90234374 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ganglioside GM2 activator level in Chronic kidney disease with hypertension and no diabetes (15441_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ganglioside GM2 activator in blood serum http://purl.obolibrary.org/obo/OBA_2041742 GCST90234375 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin B4 level in Chronic kidney disease with hypertension and no diabetes (15444_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin B4 in blood serum http://purl.obolibrary.org/obo/OBA_2043461 GCST90234376 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuregulin-1, sensory and motor neuron-derived factor isoform level in Chronic kidney disease with hypertension and no diabetes (15446_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pro-neuregulin-1, membrane-bound isoform in blood serum http://purl.obolibrary.org/obo/OBA_2044336 GCST90234377 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorbitol dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (15447_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorbitol dehydrogenase in blood serum http://purl.obolibrary.org/obo/OBA_2043598 GCST90234378 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bombesin receptor-activated protein C6orf89 level in Chronic kidney disease with hypertension and no diabetes (10885_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bombesin receptor-activated protein C6orf89 in blood serum http://purl.obolibrary.org/obo/OBA_2044835 GCST90233015 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanocortin-2 receptor accessory protein 2 level in Chronic kidney disease with hypertension and no diabetes (10889_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanocortin-2 receptor accessory protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042413 GCST90233016 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactase-like protein level in Chronic kidney disease with hypertension and no diabetes (10890_135) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lactase-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042178 GCST90233017 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretagogin level in Chronic kidney disease with hypertension and no diabetes (10894_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretagogin in blood serum http://purl.obolibrary.org/obo/OBA_2043400 GCST90233018 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protease serine 11B level in Chronic kidney disease with hypertension and no diabetes (10895_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protease serine 11B in blood serum http://purl.obolibrary.org/obo/OBA_2043882 GCST90233019 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stathmin-2 level in Chronic kidney disease with hypertension and no diabetes (10900_272) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stathmin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043702 GCST90233020 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-8 level in Chronic kidney disease with hypertension and no diabetes (10903_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-8 in blood serum http://purl.obolibrary.org/obo/OBA_2043718 GCST90233021 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurotrimin level in Chronic kidney disease with hypertension and no diabetes (10907_116) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurotrimin in blood serum http://purl.obolibrary.org/obo/OBA_2042654 GCST90233022 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 13 level in Chronic kidney disease with hypertension and no diabetes (10908_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 13 in blood serum http://purl.obolibrary.org/obo/OBA_2041662 GCST90233023 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 4 level in Chronic kidney disease with hypertension and no diabetes (10910_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040980 GCST90233024 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretory phospholipase A2 receptor level in Chronic kidney disease with hypertension and no diabetes (10916_44) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of secretory phospholipase A2 receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042916 GCST90233025 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-T2 level in Chronic kidney disease with hypertension and no diabetes (10917_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-T2 in blood serum http://purl.obolibrary.org/obo/OBA_2041754 GCST90233026 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuferricin level in Chronic kidney disease with hypertension and no diabetes (10924_258) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuferricin in blood serum http://purl.obolibrary.org/obo/OBA_2044794 GCST90233027 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-binding protein 8 level in Chronic kidney disease with hypertension and no diabetes (10933_107) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-binding protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040880 GCST90233028 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte function-associated antigen 3 level in Chronic kidney disease with hypertension and no diabetes (10938_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lymphocyte function-associated antigen 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040241 GCST90233029 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family A member 4 level in Chronic kidney disease with hypertension and no diabetes (10939_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family A member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042928 GCST90233030 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sarcalumenin level in Chronic kidney disease with hypertension and no diabetes (10940_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sarcalumenin in blood serum http://purl.obolibrary.org/obo/OBA_2043655 GCST90233031 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-6 level in Chronic kidney disease with hypertension and no diabetes (10945_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-6 in blood serum http://purl.obolibrary.org/obo/OBA_2043716 GCST90233032 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipase D3 level in Chronic kidney disease with hypertension and no diabetes (10948_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5'-3' exonuclease PLD3 in blood serum http://purl.obolibrary.org/obo/OBA_2042922 GCST90233033 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S acidic ribosomal protein P2 level in Chronic kidney disease with hypertension and no diabetes (10949_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S acidic ribosomal protein P2 in blood serum http://purl.obolibrary.org/obo/OBA_2043324 GCST90233034 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 2 member A level in Chronic kidney disease with hypertension and no diabetes (10953_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 2 member A in blood serum http://purl.obolibrary.org/obo/OBA_2041044 GCST90233035 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 10 member A level in Chronic kidney disease with hypertension and no diabetes (10955_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 10 member A in blood serum http://purl.obolibrary.org/obo/OBA_2040297 GCST90233036 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycine cleavage system H protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (10956_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycine cleavage system H protein, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041694 GCST90233037 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BET1-like protein level in Chronic kidney disease with hypertension and no diabetes (10959_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BET1-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2040793 GCST90233038 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoic acid receptor responder protein 3 level in Chronic kidney disease with hypertension and no diabetes (10961_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipase A and acyltransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043199 GCST90233039 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 3 level in Chronic kidney disease with hypertension and no diabetes (3432_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-a receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0020352 GCST90237378 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follistatin-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (3438_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 follistatin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020394 GCST90237379 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granzyme A level in Chronic kidney disease with hypertension and no diabetes (3440_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 granzyme A measurement http://www.ebi.ac.uk/efo/EFO_0008145 GCST90237380 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycogen synthase kinase-3 alpha level in Chronic kidney disease with hypertension and no diabetes (3441_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 glycogen synthase kinase-3 alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0020412 GCST90237381 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-15 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3445_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-15 receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042001 GCST90237382 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-18 receptor 1 level in Chronic kidney disease with hypertension and no diabetes (3446_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-18 receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040284 GCST90237383 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-8 level in Chronic kidney disease with hypertension and no diabetes (3447_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-8 measurement http://www.ebi.ac.uk/efo/EFO_0004811 GCST90237384 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin receptor level in Chronic kidney disease with hypertension and no diabetes (3448_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin receptor measurement http://www.ebi.ac.uk/efo/EFO_0008160 GCST90237385 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallistatin level in Chronic kidney disease with hypertension and no diabetes (3449_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 kallistatin measurement http://www.ebi.ac.uk/efo/EFO_0008196 GCST90237386 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-6 level in Chronic kidney disease with hypertension and no diabetes (3450_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of kallikrein-6 in blood serum http://purl.obolibrary.org/obo/OBA_2042128 GCST90237387 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase Lck level in Chronic kidney disease with hypertension and no diabetes (3452_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase LCK measurement http://www.ebi.ac.uk/efo/EFO_0020826 GCST90237388 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase Lyn level in Chronic kidney disease with hypertension and no diabetes (3453_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase lyn measurement http://www.ebi.ac.uk/efo/EFO_0020827 GCST90237389 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Periostin level in Chronic kidney disease with hypertension and no diabetes (3457_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 periostin measurement http://www.ebi.ac.uk/efo/EFO_0020628 GCST90237390 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor receptor beta level in Chronic kidney disease with hypertension and no diabetes (3459_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 platelet-derived growth factor receptor beta measurement http://www.ebi.ac.uk/efo/EFO_0008265 GCST90237391 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brevican core protein level in Chronic kidney disease with hypertension and no diabetes (3461_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 brevican core protein measurement http://www.ebi.ac.uk/efo/EFO_0020193 GCST90237392 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-dependent protein kinase catalytic subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3466_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 cAMP-dependent protein kinase catalytic subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020222 GCST90237393 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosomal protein S6 kinase alpha-3 level in Chronic kidney disease with hypertension and no diabetes (3469_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 ribosomal protein s6 kinase alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020709 GCST90237394 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E-selectin level in Chronic kidney disease with hypertension and no diabetes (3470_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 e-selectin measurement http://www.ebi.ac.uk/efo/EFO_0004575 GCST90237395 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase 16 level in Chronic kidney disease with hypertension and no diabetes (3471_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase 16 measurement http://www.ebi.ac.uk/efo/EFO_0020724 GCST90237396 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Baculoviral IAP repeat-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (3472_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 baculoviral IAP repeat-containing protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020174 GCST90237397 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombopoietin Receptor level in Chronic kidney disease with hypertension and no diabetes (3473_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 thrombopoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020769 GCST90237398 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High affinity nerve growth factor receptor level in Chronic kidney disease with hypertension and no diabetes (3477_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 high affinity nerve growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0020448 GCST90237399 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trypsin-3 level in Chronic kidney disease with hypertension and no diabetes (3479_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 trypsin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020791 GCST90237400 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 3 level in Chronic kidney disease with hypertension and no diabetes (3480_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 dual specificity protein phosphatase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020336 GCST90237401 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Xaa-Pro aminopeptidase 1 level in Chronic kidney disease with hypertension and no diabetes (3481_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 xaa-pro aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020856 GCST90237402 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aromatic-L-amino-acid decarboxylase level in Chronic kidney disease with hypertension and no diabetes (3538_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 aromatic-l-amino-acid decarboxylase measurement http://www.ebi.ac.uk/efo/EFO_0020161 GCST90237428 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adiponectin level in Chronic kidney disease with hypertension and no diabetes (3554_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 adiponectin measurement http://www.ebi.ac.uk/efo/EFO_0004502 GCST90237429 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1-antitrypsin level in Chronic kidney disease with hypertension and no diabetes (3580_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 alpha-1-antitrypsin measurement http://www.ebi.ac.uk/efo/EFO_0008327 GCST90237430 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-2-HS-glycoprotein level in Chronic kidney disease with hypertension and no diabetes (3581_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 alpha-2-HS-glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008020 GCST90237431 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arylsulfatase A level in Chronic kidney disease with hypertension and no diabetes (3583_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90237432 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Basigin level in Chronic kidney disease with hypertension and no diabetes (3585_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 basigin measurement http://www.ebi.ac.uk/efo/EFO_0020176 GCST90237433 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 10 level in Chronic kidney disease with hypertension and no diabetes (3587_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 bone morphogenetic protein 10 measurement http://www.ebi.ac.uk/efo/EFO_0020185 GCST90237434 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-6 level in Chronic kidney disease with hypertension and no diabetes (3591_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 cadherin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020214 GCST90237435 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase type 1 level in Chronic kidney disease with hypertension and no diabetes (3592_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcium/calmodulin-dependent protein kinase type 1 measurement http://www.ebi.ac.uk/efo/EFO_0008062 GCST90237436 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-3 level in Chronic kidney disease with hypertension and no diabetes (3593_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 caspase-3 measurement http://www.ebi.ac.uk/efo/EFO_0008070 GCST90237437 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chitotriosidase-1 level in Chronic kidney disease with hypertension and no diabetes (3600_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 chitotriosidase-1 measurement http://www.ebi.ac.uk/efo/EFO_0008084 GCST90237438 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neural cell adhesion molecule L1-like protein level in Chronic kidney disease with hypertension and no diabetes (3601_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 neural cell adhesion molecule l1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020595 GCST90237439 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 7 member A level in Chronic kidney disease with hypertension and no diabetes (3603_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 7 member A in blood serum http://purl.obolibrary.org/obo/OBA_2040330 GCST90237440 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mannan-binding lectin serine protease 1 level in Chronic kidney disease with hypertension and no diabetes (3605_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90237441 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dickkopf-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (3607_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 Dickkopf-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008109 GCST90237442 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelin-converting enzyme 1 level in Chronic kidney disease with hypertension and no diabetes (3611_70) 466 African American individuals NA Illumina [14870897] (imputed) 1 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90237443 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ficolin-1 level in Chronic kidney disease with hypertension and no diabetes (3613_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90237444 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylglucosamine-6-sulfatase level in Chronic kidney disease with hypertension and no diabetes (3616_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90237445 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte growth factor activator level in Chronic kidney disease with hypertension and no diabetes (3617_80) 466 African American individuals NA Illumina [14870897] (imputed) 1 hepatocyte growth factor activator measurement http://www.ebi.ac.uk/efo/EFO_0008152 GCST90237446 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-22 receptor subunit alpha-1 level in Chronic kidney disease with hypertension and no diabetes (3620_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90237447 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Legumain level in Chronic kidney disease with hypertension and no diabetes (3622_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 legumain measurement http://www.ebi.ac.uk/efo/EFO_0020530 GCST90237448 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte antigen 86 level in Chronic kidney disease with hypertension and no diabetes (3623_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphocyte antigen 86 measurement http://www.ebi.ac.uk/efo/EFO_0020541 GCST90237449 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Progonadoliberin-2 level in Chronic kidney disease with hypertension and no diabetes (10708_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of progonadoliberin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041760 GCST90232962 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zona pellucida-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (10710_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zona pellucida-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044219 GCST90232963 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 7 level in Chronic kidney disease with hypertension and no diabetes (10713_151) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMRF35-like molecule 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040942 GCST90232964 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase PAK 5 level in Chronic kidney disease with hypertension and no diabetes (3388_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase PAK 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042751 GCST90237353 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PIK3CA/PIK3R1 level in Chronic kidney disease with hypertension and no diabetes (3390_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 PIK3CA/PIK3R1 measurement http://www.ebi.ac.uk/efo/EFO_0021971 GCST90237354 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform level in Chronic kidney disease with hypertension and no diabetes (3391_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform measurement http://www.ebi.ac.uk/efo/EFO_0020637 GCST90237355 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase B gamma level in Chronic kidney disease with hypertension and no diabetes (3392_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RAC-gamma serine/threonine-protein kinase in blood serum http://purl.obolibrary.org/obo/OBA_2040556 GCST90237356 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase PLK1 level in Chronic kidney disease with hypertension and no diabetes (3394_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase PLK1 measurement http://www.ebi.ac.uk/efo/EFO_0020732 GCST90237357 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Renin level in Chronic kidney disease with hypertension and no diabetes (3396_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 renin measurement http://www.ebi.ac.uk/efo/EFO_0010616 GCST90237358 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 11 level in Chronic kidney disease with hypertension and no diabetes (3397_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90237359 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stabilin-2 level in Chronic kidney disease with hypertension and no diabetes (3399_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 stabilin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020752 GCST90237360 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 2 level in Chronic kidney disease with hypertension and no diabetes (3401_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein phosphatase non-receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0020836 GCST90237361 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptase beta-2 level in Chronic kidney disease with hypertension and no diabetes (3403_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 tryptase beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0008306 GCST90237362 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptase gamma level in Chronic kidney disease with hypertension and no diabetes (3404_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 tryptase gamma measurement http://www.ebi.ac.uk/efo/EFO_0020792 GCST90237363 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-fold modifier-conjugating enzyme 1 level in Chronic kidney disease with hypertension and no diabetes (3405_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin-fold modifier-conjugating enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020843 GCST90237364 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apoptosis regulator Bcl-2 level in Chronic kidney disease with hypertension and no diabetes (3412_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 apoptosis regulator BCL-2 measurement http://www.ebi.ac.uk/efo/EFO_0020159 GCST90237365 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bcl-2-related protein A1 level in Chronic kidney disease with hypertension and no diabetes (3413_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 BCL-2-related protein A1 measurement http://www.ebi.ac.uk/efo/EFO_0020178 GCST90237366 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoplasmic tyrosine-protein kinase BMX level in Chronic kidney disease with hypertension and no diabetes (3414_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytoplasmic tyrosine-protein kinase BMX measurement http://www.ebi.ac.uk/efo/EFO_0020308 GCST90237367 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone sialoprotein 2 level in Chronic kidney disease with hypertension and no diabetes (3415_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 bone sialoprotein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020190 GCST90237368 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase BTK level in Chronic kidney disease with hypertension and no diabetes (3416_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase BTK measurement http://www.ebi.ac.uk/efo/EFO_0020819 GCST90237369 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase type 1D level in Chronic kidney disease with hypertension and no diabetes (3418_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 calcium/calmodulin-dependent protein kinase type 1D measurement http://www.ebi.ac.uk/efo/EFO_0008063 GCST90237370 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase type II subunit delta level in Chronic kidney disease with hypertension and no diabetes (3419_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcium/calmodulin-dependent protein kinase type II subunit delta measurement http://www.ebi.ac.uk/efo/EFO_0020220 GCST90237371 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 13 level in Chronic kidney disease with hypertension and no diabetes (3420_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase 13 measurement http://www.ebi.ac.uk/efo/EFO_0008067 GCST90237372 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 8 level in Chronic kidney disease with hypertension and no diabetes (3421_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 8 measurement http://www.ebi.ac.uk/efo/EFO_0010592 GCST90237373 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 1:G2/mitotic-specific cyclin-B1 complex level in Chronic kidney disease with hypertension and no diabetes (3422_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 cyclin-dependent kinase 1:g2/mitotic-specific cyclin-B1 complex measurement http://www.ebi.ac.uk/efo/EFO_0020294 GCST90237374 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymase level in Chronic kidney disease with hypertension and no diabetes (3423_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 chymase measurement http://www.ebi.ac.uk/efo/EFO_0020259 GCST90237375 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase II subunit alpha level in Chronic kidney disease with hypertension and no diabetes (3427_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 casein kinase II subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020238 GCST90237376 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 1 level in Chronic kidney disease with hypertension and no diabetes (3431_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 ephrin type-A receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008123 GCST90237377 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiotensinogen level in Chronic kidney disease with hypertension and no diabetes (3484_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiotensinogen measurement http://www.ebi.ac.uk/efo/EFO_0008025 GCST90237403 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-2-microglobulin level in Chronic kidney disease with hypertension and no diabetes (3485_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 beta-2-microglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020180 GCST90237404 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 1 level in Chronic kidney disease with hypertension and no diabetes (3486_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020375 GCST90237405 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 13 level in Chronic kidney disease with hypertension and no diabetes (3487_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-X-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020205 GCST90237406 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catalase level in Chronic kidney disease with hypertension and no diabetes (3488_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 catalase measurement http://www.ebi.ac.uk/efo/EFO_0008071 GCST90237407 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ciliary neurotrophic factor level in Chronic kidney disease with hypertension and no diabetes (3489_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 ciliary neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020260 GCST90237408 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 17 level in Chronic kidney disease with hypertension and no diabetes (3494_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 17 measurement http://www.ebi.ac.uk/efo/EFO_0020379 GCST90237409 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 6 level in Chronic kidney disease with hypertension and no diabetes (3495_15) 466 African American individuals NA Illumina [14870897] (imputed) 7 C-X-C motif chemokine 6 measurement http://www.ebi.ac.uk/efo/EFO_0008059 GCST90237410 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-2 level in Chronic kidney disease with hypertension and no diabetes (3497_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 interferon alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020483 GCST90237411 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17A level in Chronic kidney disease with hypertension and no diabetes (3498_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90237412 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17B level in Chronic kidney disease with hypertension and no diabetes (3499_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17B measurement http://www.ebi.ac.uk/efo/EFO_0021973 GCST90237413 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-I: beta-1 complex level in Chronic kidney disease with hypertension and no diabetes (3503_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-I: beta-1 complex measurement http://www.ebi.ac.uk/efo/EFO_0008162 GCST90237414 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepcidin level in Chronic kidney disease with hypertension and no diabetes (3504_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 hepcidin measurement http://www.ebi.ac.uk/efo/EFO_0020440 GCST90237415 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphotoxin alpha1:beta2 level in Chronic kidney disease with hypertension and no diabetes (3505_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphotoxin alpha1:beta2 measurement http://www.ebi.ac.uk/efo/EFO_0020542 GCST90237416 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphotoxin alpha2:beta1 level in Chronic kidney disease with hypertension and no diabetes (3506_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphotoxin alpha2:beta1 measurement http://www.ebi.ac.uk/efo/EFO_0020543 GCST90237417 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 22 level in Chronic kidney disease with hypertension and no diabetes (3508_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90237418 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 15 level in Chronic kidney disease with hypertension and no diabetes (3509_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90237419 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myeloblastin level in Chronic kidney disease with hypertension and no diabetes (3514_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 myeloblastin measurement http://www.ebi.ac.uk/efo/EFO_0020585 GCST90237420 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal cell-derived factor 1 level in Chronic kidney disease with hypertension and no diabetes (3516_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 stromal cell-derived factor 1 alpha measurement http://www.ebi.ac.uk/efo/EFO_0008293 GCST90237421 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase B2 level in Chronic kidney disease with hypertension and no diabetes (3518_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 carboxypeptidase B2 measurement http://www.ebi.ac.uk/efo/EFO_0008069 GCST90237422 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 17 level in Chronic kidney disease with hypertension and no diabetes (3519_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 17 measurement http://www.ebi.ac.uk/efo/EFO_0008045 GCST90237423 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming growth factor beta-3 level in Chronic kidney disease with hypertension and no diabetes (3520_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 transforming growth factor beta-3 measurement http://www.ebi.ac.uk/efo/EFO_0020782 GCST90237424 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyroid Stimulating Hormone level in Chronic kidney disease with hypertension and no diabetes (3521_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 thyroid stimulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0004748 GCST90237425 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vasoactive Intestinal Peptide level in Chronic kidney disease with hypertension and no diabetes (3522_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 vasoactive intestinal peptide measurement http://www.ebi.ac.uk/efo/EFO_0020849 GCST90237426 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dickkopf-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (3535_84) 466 African American individuals NA Illumina [14870897] (imputed) 1 dickkopf‐related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0010620 GCST90237427 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming acidic coiled-coil-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (22027_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transforming acidic coiled-coil-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043765 GCST90235968 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Wiskott-Aldrich syndrome protein level in Chronic kidney disease with hypertension and no diabetes (22033_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin nucleation-promoting factor WAS in blood serum http://purl.obolibrary.org/obo/OBA_2044124 GCST90235969 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Wiskott-Aldrich syndrome protein level in Chronic kidney disease with hypertension and no diabetes (22033_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin nucleation-promoting factor WAS in blood serum http://purl.obolibrary.org/obo/OBA_2044124 GCST90235970 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger and BTB domain-containing protein 16 level in Chronic kidney disease with hypertension and no diabetes (22034_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger and BTB domain-containing protein 16 in blood serum http://purl.obolibrary.org/obo/OBA_2044172 GCST90235971 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EF-hand domain-containing protein D2 level in Chronic kidney disease with hypertension and no diabetes (22037_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EF-hand domain-containing protein D2 in blood serum http://purl.obolibrary.org/obo/OBA_2044289 GCST90235972 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity mitogen-activated protein kinase kinase 5 level in Chronic kidney disease with hypertension and no diabetes (22041_26) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of dual specificity mitogen-activated protein kinase kinase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042285 GCST90235973 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock-related 70 kDa protein 2 level in Chronic kidney disease with hypertension and no diabetes (22043_174) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock-related 70 kDa protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041947 GCST90235974 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small ubiquitin-related modifier 4 level in Chronic kidney disease with hypertension and no diabetes (22045_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small ubiquitin-related modifier 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043735 GCST90235975 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(V) chain level in Chronic kidney disease with hypertension and no diabetes (22047_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(V) chain in blood serum http://purl.obolibrary.org/obo/OBA_2040437 GCST90235976 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein eta level in Chronic kidney disease with hypertension and no diabetes (22049_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 14-3-3 protein eta in blood serum http://purl.obolibrary.org/obo/OBA_2044167 GCST90235977 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. KxDL motif-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (22050_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of KxDL motif-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044652 GCST90235978 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein O1A level in Chronic kidney disease with hypertension and no diabetes (22055_31) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of forkhead box protein O1 in blood serum http://purl.obolibrary.org/obo/OBA_2041610 GCST90235979 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldehyde dehydrogenase X, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22057_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldehyde dehydrogenase X, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040561 GCST90235980 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Palmdelphin level in Chronic kidney disease with hypertension and no diabetes (22059_56) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of palmdelphin in blood serum http://purl.obolibrary.org/obo/OBA_2042753 GCST90235981 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpain small subunit 2 level in Chronic kidney disease with hypertension and no diabetes (22063_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calpain small subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040893 GCST90235982 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 8 level in Chronic kidney disease with hypertension and no diabetes (22065_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon regulatory factor 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040379 GCST90235983 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform level in Chronic kidney disease with hypertension and no diabetes (22068_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform in blood serum http://purl.obolibrary.org/obo/OBA_2043011 GCST90235984 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho guanine nucleotide exchange factor 16 level in Chronic kidney disease with hypertension and no diabetes (22070_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho guanine nucleotide exchange factor 16 in blood serum http://purl.obolibrary.org/obo/OBA_2040659 GCST90235985 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat and SOCS box protein 8 level in Chronic kidney disease with hypertension and no diabetes (22071_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat and SOCS box protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040692 GCST90235986 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP synthase B chain, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22073_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP synthase F(0) complex subunit B1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040729 GCST90235987 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ataxin-2-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (22074_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA binding protein fox-1 homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041605 GCST90235988 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-dependent transcription factor ATF-3 level in Chronic kidney disease with hypertension and no diabetes (22075_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-dependent transcription factor ATF-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040713 GCST90235989 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein atonal homolog 1 level in Chronic kidney disease with hypertension and no diabetes (22076_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor ATOH1 in blood serum http://purl.obolibrary.org/obo/OBA_2040724 GCST90235990 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial inner membrane protease ATP23 homolog level in Chronic kidney disease with hypertension and no diabetes (22077_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial inner membrane protease ATP23 in blood serum http://purl.obolibrary.org/obo/OBA_2044154 GCST90235991 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine aminotransferase level in Chronic kidney disease with hypertension and no diabetes (22078_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine aminotransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043780 GCST90235992 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sequestosome-1 level in Chronic kidney disease with hypertension and no diabetes (15448_47) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sequestosome-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043649 GCST90234379 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5'-Nucleotidase level in Chronic kidney disease with hypertension and no diabetes (15452_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 5'-nucleotidase in blood serum http://purl.obolibrary.org/obo/OBA_2040327 GCST90234380 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1-microglobulin level in Chronic kidney disease with hypertension and no diabetes (15453_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein AMBP in blood serum http://purl.obolibrary.org/obo/OBA_2040579 GCST90234381 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 15 level in Chronic kidney disease with hypertension and no diabetes (15455_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234382 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dipeptidyl peptidase 4 level in Chronic kidney disease with hypertension and no diabetes (15460_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dipeptidyl peptidase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040271 GCST90234383 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD8 alpha chain level in Chronic kidney disease with hypertension and no diabetes (15462_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of T-cell surface glycoprotein CD8 alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040238 GCST90234384 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein canopy homolog 4 level in Chronic kidney disease with hypertension and no diabetes (15465_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein canopy homolog 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041071 GCST90234385 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(IX) chain level in Chronic kidney disease with hypertension and no diabetes (15466_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(IX) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041087 GCST90234386 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen triple helix repeat-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (15467_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen triple helix repeat-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041185 GCST90234387 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (15468_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement factor H-related protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0600054 GCST90234388 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-hexosaminidase subunit beta level in Chronic kidney disease with hypertension and no diabetes (15470_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-hexosaminidase subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2041865 GCST90234389 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pancreatic lipase-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (15471_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pancreatic lipase-related protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042950 GCST90234390 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 11 level in Chronic kidney disease with hypertension and no diabetes (15472_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of low-density lipoprotein receptor-related protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042229 GCST90234391 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 level in Chronic kidney disease with hypertension and no diabetes (15474_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042894 GCST90234392 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipid transfer protein level in Chronic kidney disease with hypertension and no diabetes (15475_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of phospholipid transfer protein in blood serum http://purl.obolibrary.org/obo/OBA_2042934 GCST90234393 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regenerating islet-derived protein 3-gamma level in Chronic kidney disease with hypertension and no diabetes (15476_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of regenerating islet-derived protein 3-gamma in blood serum http://purl.obolibrary.org/obo/OBA_2043233 GCST90234394 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular non-inflammatory molecule 2 level in Chronic kidney disease with hypertension and no diabetes (15480_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pantetheine hydrolase VNN2 in blood serum http://purl.obolibrary.org/obo/OBA_2044105 GCST90234395 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Antibacterial protein LL-37 level in Chronic kidney disease with hypertension and no diabetes (15481_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cathelicidin antimicrobial peptide in blood serum http://purl.obolibrary.org/obo/OBA_2044228 GCST90234396 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-2-macroglobulin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (15482_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of alpha-2-macroglobulin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040450 GCST90234397 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Agrin level in Chronic kidney disease with hypertension and no diabetes (15483_377) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of agrin in blood serum http://purl.obolibrary.org/obo/OBA_2040538 GCST90234398 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amiloride-sensitive amine oxidase [copper-containing] level in Chronic kidney disease with hypertension and no diabetes (15486_126) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of amiloride-sensitive amine oxidase [copper-containing] in blood serum http://purl.obolibrary.org/obo/OBA_2040464 GCST90234399 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Liver carboxylesterase 1 level in Chronic kidney disease with hypertension and no diabetes (15487_164) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of liver carboxylesterase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040989 GCST90234400 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endosialin level in Chronic kidney disease with hypertension and no diabetes (15491_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of endosialin in blood serum http://purl.obolibrary.org/obo/OBA_2040273 GCST90234401 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich motor neuron 1 protein level in Chronic kidney disease with hypertension and no diabetes (15492_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90234402 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (15494_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041576 GCST90234403 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Corticosteroid 11-beta-dehydrogenase isozyme 1 level in Chronic kidney disease with hypertension and no diabetes (21967_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 11-beta-hydroxysteroid dehydrogenase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041938 GCST90235943 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dipeptidyl aminopeptidase-like protein 6 level in Chronic kidney disease with hypertension and no diabetes (21969_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dipeptidyl aminopeptidase-like protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041353 GCST90235944 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Friend leukemia integration 1 transcription factor level in Chronic kidney disease with hypertension and no diabetes (21971_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Friend leukemia integration 1 transcription factor in blood serum http://purl.obolibrary.org/obo/OBA_2041593 GCST90235945 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. I-kappa-B kinase gamma level in Chronic kidney disease with hypertension and no diabetes (21976_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NF-kappa-B essential modulator in blood serum http://purl.obolibrary.org/obo/OBA_2040322 GCST90235946 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-6 level in Chronic kidney disease with hypertension and no diabetes (21979_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin alpha-6 in blood serum http://purl.obolibrary.org/obo/OBA_2042048 GCST90235947 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-6 level in Chronic kidney disease with hypertension and no diabetes (21979_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin alpha-6 in blood serum http://purl.obolibrary.org/obo/OBA_2042048 GCST90235948 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-M level in Chronic kidney disease with hypertension and no diabetes (21981_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin alpha-M in blood serum http://purl.obolibrary.org/obo/OBA_2040228 GCST90235949 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin beta-1-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (21985_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin beta-1-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042050 GCST90235950 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lipoprotein lipase level in Chronic kidney disease with hypertension and no diabetes (21987_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lipoprotein lipase in blood serum http://purl.obolibrary.org/obo/OBA_2042223 GCST90235951 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase kinase kinase kinase 5 level in Chronic kidney disease with hypertension and no diabetes (21989_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase kinase kinase kinase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042291 GCST90235952 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurabin-2 level in Chronic kidney disease with hypertension and no diabetes (21991_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurabin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043006 GCST90235953 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NOS level in Chronic kidney disease with hypertension and no diabetes (21995_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nitric oxide synthase, endothelial in blood serum http://purl.obolibrary.org/obo/OBA_2042607 GCST90235954 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD8 ultimate buster 1 level in Chronic kidney disease with hypertension and no diabetes (21996_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD8 ultimate buster 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042657 GCST90235955 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleobindin-2 level in Chronic kidney disease with hypertension and no diabetes (21999_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleobindin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042661 GCST90235956 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-arginine deiminase type-2 level in Chronic kidney disease with hypertension and no diabetes (22001_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-arginine deiminase type-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042741 GCST90235957 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paraoxonase 2 level in Chronic kidney disease with hypertension and no diabetes (22003_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serum paraoxonase/arylesterase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042974 GCST90235958 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. [Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22005_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of [pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042836 GCST90235959 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Resistin-like beta level in Chronic kidney disease with hypertension and no diabetes (22007_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of resistin-like beta in blood serum http://purl.obolibrary.org/obo/OBA_2043243 GCST90235960 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1B level in Chronic kidney disease with hypertension and no diabetes (22009_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein phosphatase 1B in blood serum http://purl.obolibrary.org/obo/OBA_2042992 GCST90235961 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon-inducible double-stranded RNA-dependent protein kinase activator A level in Chronic kidney disease with hypertension and no diabetes (22010_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interferon-inducible double-stranded RNA-dependent protein kinase activator A in blood serum http://purl.obolibrary.org/obo/OBA_2043031 GCST90235962 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras association domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (22013_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras association domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043200 GCST90235963 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase TRIM21 level in Chronic kidney disease with hypertension and no diabetes (22015_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase TRIM21 in blood serum http://purl.obolibrary.org/obo/OBA_2043933 GCST90235964 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH2B adapter protein 3 level in Chronic kidney disease with hypertension and no diabetes (22019_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH2B adapter protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043488 GCST90235965 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endostatin level in Chronic kidney disease with hypertension and no diabetes (2201_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 endostatin measurement http://www.ebi.ac.uk/efo/EFO_0020347 GCST90235966 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kynurenine/alpha-aminoadipate aminotransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22023_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of kynurenine/alpha-aminoadipate aminotransferase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040454 GCST90235967 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Folate receptor gamma level in Chronic kidney disease with hypertension and no diabetes (15495_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of folate receptor gamma in blood serum http://purl.obolibrary.org/obo/OBA_2041603 GCST90234404 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan sulfate glucosamine 3-O-sulfotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (15497_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heparan sulfate glucosamine 3-O-sulfotransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041930 GCST90234405 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Attractin level in Chronic kidney disease with hypertension and no diabetes (15499_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of attractin in blood serum http://purl.obolibrary.org/obo/OBA_2040736 GCST90234406 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Left-right determination factor 2 level in Chronic kidney disease with hypertension and no diabetes (15503_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lefty 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040213 GCST90234407 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Left-right determination factor 2 level in Chronic kidney disease with hypertension and no diabetes (15503_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lefty 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040213 GCST90234408 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Baculoviral IAP repeat-containing protein 7 Isoform beta level in Chronic kidney disease with hypertension and no diabetes (15504_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 baculoviral IAP repeat-containing protein 7 isoform beta measurement http://www.ebi.ac.uk/efo/EFO_0020175 GCST90234409 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 12 level in Chronic kidney disease with hypertension and no diabetes (15506_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor-related protein 12 in blood serum http://purl.obolibrary.org/obo/OBA_2042230 GCST90234410 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylglucosaminidase level in Chronic kidney disease with hypertension and no diabetes (15509_2) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of alpha-N-acetylglucosaminidase in blood serum http://purl.obolibrary.org/obo/OBA_2042500 GCST90234411 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal pentraxin receptor level in Chronic kidney disease with hypertension and no diabetes (15511_37) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of neuronal pentraxin receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042624 GCST90234412 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostasin level in Chronic kidney disease with hypertension and no diabetes (15513_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostasin in blood serum http://purl.obolibrary.org/obo/OBA_2043048 GCST90234413 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cholinesterase level in Chronic kidney disease with hypertension and no diabetes (15514_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cholinesterase in blood serum http://purl.obolibrary.org/obo/OBA_2040786 GCST90234414 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum amyloid A-1 protein level in Chronic kidney disease with hypertension and no diabetes (15515_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90234415 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum amyloid A-4 protein level in Chronic kidney disease with hypertension and no diabetes (15516_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of primate-type serum amyloid A-4 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043373 GCST90234416 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calsyntenin-1 level in Chronic kidney disease with hypertension and no diabetes (15521_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calsyntenin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041056 GCST90234417 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Golgi-associated plant pathogenesis-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (15522_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Golgi-associated plant pathogenesis-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041730 GCST90234418 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta-aminolevulinic acid dehydratase level in Chronic kidney disease with hypertension and no diabetes (15523_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of delta-aminolevulinic acid dehydratase in blood serum http://purl.obolibrary.org/obo/OBA_2040557 GCST90234419 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase 1C level in Chronic kidney disease with hypertension and no diabetes (15525_294) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alcohol dehydrogenase 1C in blood serum http://purl.obolibrary.org/obo/OBA_2040515 GCST90234420 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione synthetase level in Chronic kidney disease with hypertension and no diabetes (15526_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione synthetase in blood serum http://purl.obolibrary.org/obo/OBA_2041801 GCST90234421 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydrolipoyl dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (15527_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydrolipoyl dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041308 GCST90234422 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-B receptor 4 level in Chronic kidney disease with hypertension and no diabetes (15530_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-b receptor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020354 GCST90234423 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage scavenger receptor types I and II level in Chronic kidney disease with hypertension and no diabetes (15533_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90234424 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Malate dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (15534_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of malate dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042318 GCST90234425 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease 27 level in Chronic kidney disease with hypertension and no diabetes (15535_3) 466 African American individuals NA Illumina [14870897] (imputed) 2 serine protease 27 measurement http://www.ebi.ac.uk/efo/EFO_0008280 GCST90234426 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT and NTRK-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (15539_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 SLIT and NTRK-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021974 GCST90234427 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vimentin level in Chronic kidney disease with hypertension and no diabetes (15540_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vimentin in blood serum http://purl.obolibrary.org/obo/OBA_2044101 GCST90234428 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Creatine kinase U-type, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (15542_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of creatine kinase U-type, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041037 GCST90234429 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-14 level in Chronic kidney disease with hypertension and no diabetes (15544_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90234430 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcineurin subunit B type 1 level in Chronic kidney disease with hypertension and no diabetes (15545_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcineurin subunit B type 1 measurement http://www.ebi.ac.uk/efo/EFO_0020215 GCST90234431 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. D-3-phosphoglycerate dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (15548_35) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of D-3-phosphoglycerate dehydrogenase in blood serum http://purl.obolibrary.org/obo/OBA_2042875 GCST90234432 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acetylcholinesterase level in Chronic kidney disease with hypertension and no diabetes (15553_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acetylcholinesterase in blood serum http://purl.obolibrary.org/obo/OBA_2040477 GCST90234433 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-amylase 2B level in Chronic kidney disease with hypertension and no diabetes (15556_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-amylase 2B in blood serum http://purl.obolibrary.org/obo/OBA_2040586 GCST90234434 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamyl aminopeptidase level in Chronic kidney disease with hypertension and no diabetes (15558_63) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutamyl aminopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2040370 GCST90234435 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anthrax toxin receptor 2 level in Chronic kidney disease with hypertension and no diabetes (15559_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anthrax toxin receptor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040596 GCST90234436 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-glucuronidase level in Chronic kidney disease with hypertension and no diabetes (15562_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-glucuronidase in blood serum http://purl.obolibrary.org/obo/OBA_2041824 GCST90234437 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mucin-16 level in Chronic kidney disease with hypertension and no diabetes (15565_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mucin-16 in blood serum http://purl.obolibrary.org/obo/OBA_2042459 GCST90234438 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calponin-1 level in Chronic kidney disease with hypertension and no diabetes (15566_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calponin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041066 GCST90234439 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD3 zeta chain level in Chronic kidney disease with hypertension and no diabetes (15567_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-cell surface glycoprotein CD3 in blood serum http://purl.obolibrary.org/obo/OBA_2040232 GCST90234440 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen Type II level in Chronic kidney disease with hypertension and no diabetes (15569_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen type II alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040427 GCST90234441 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement receptor type 2 level in Chronic kidney disease with hypertension and no diabetes (15570_99) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement receptor type 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040270 GCST90234442 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurocan core protein level in Chronic kidney disease with hypertension and no diabetes (15573_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurocan core protein in blood serum http://purl.obolibrary.org/obo/OBA_2042522 GCST90234443 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-A2 level in Chronic kidney disease with hypertension and no diabetes (15574_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-A2 in blood serum http://purl.obolibrary.org/obo/OBA_2040932 GCST90234444 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleotide pyrophosphatase/phosphodiesterase family member 6 level in Chronic kidney disease with hypertension and no diabetes (15579_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycerophosphocholine cholinephosphodiesterase ENPP6 in blood serum http://purl.obolibrary.org/obo/OBA_2041482 GCST90234445 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 7 level in Chronic kidney disease with hypertension and no diabetes (15580_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ephrin type-A receptor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041491 GCST90234446 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibronectin type 3 and ankyrin repeat domains protein 1 level in Chronic kidney disease with hypertension and no diabetes (15581_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibronectin type 3 and ankyrin repeat domains protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044753 GCST90234447 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ficolin-1 level in Chronic kidney disease with hypertension and no diabetes (15582_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90234448 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fc receptor-like B level in Chronic kidney disease with hypertension and no diabetes (15583_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fc receptor-like B in blood serum http://purl.obolibrary.org/obo/OBA_2041567 GCST90234449 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (15584_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement factor H-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0600055 GCST90234450 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibulin-5 level in Chronic kidney disease with hypertension and no diabetes (15585_304) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibulin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2041553 GCST90234451 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Folate receptor beta level in Chronic kidney disease with hypertension and no diabetes (15587_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of folate receptor beta in blood serum http://purl.obolibrary.org/obo/OBA_2041602 GCST90234452 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-galactosidase A level in Chronic kidney disease with hypertension and no diabetes (15588_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-galactosidase A in blood serum http://purl.obolibrary.org/obo/OBA_2041726 GCST90234453 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitamin D-binding protein level in Chronic kidney disease with hypertension and no diabetes (15589_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 vitamin D-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0005675 GCST90234454 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione peroxidase 1 level in Chronic kidney disease with hypertension and no diabetes (15591_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 blood glutathione peroxidase measurement http://www.ebi.ac.uk/efo/EFO_0600071 GCST90234455 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease HTRA1 level in Chronic kidney disease with hypertension and no diabetes (15594_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine protease HTRA1 in blood serum http://purl.obolibrary.org/obo/OBA_2041959 GCST90234456 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein HEXIM1 level in Chronic kidney disease with hypertension and no diabetes (15596_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein HEXIM1 in blood serum http://purl.obolibrary.org/obo/OBA_2041866 GCST90234457 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-6 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (15602_43) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-6 receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040293 GCST90234458 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-2 level in Chronic kidney disease with hypertension and no diabetes (15603_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin alpha-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040226 GCST90234459 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 9 level in Chronic kidney disease with hypertension and no diabetes (15604_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020581 GCST90234460 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type I cytoskeletal 19 level in Chronic kidney disease with hypertension and no diabetes (15606_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type I cytoskeletal 19 in blood serum http://purl.obolibrary.org/obo/OBA_2042141 GCST90234461 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyruvate kinase PKLR level in Chronic kidney disease with hypertension and no diabetes (15607_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyruvate kinase PKLR in blood serum http://purl.obolibrary.org/obo/OBA_2042906 GCST90234462 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosomal protein S6 kinase beta-1 level in Chronic kidney disease with hypertension and no diabetes (15608_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosomal protein S6 kinase beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040200 GCST90234463 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosol aminopeptidase level in Chronic kidney disease with hypertension and no diabetes (15610_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosol aminopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2042163 GCST90234464 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein lin-7 homolog B level in Chronic kidney disease with hypertension and no diabetes (15612_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein lin-7 homolog B measurement http://www.ebi.ac.uk/efo/EFO_0021978 GCST90234465 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pancreatic triacylglycerol lipase level in Chronic kidney disease with hypertension and no diabetes (15613_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pancreatic triacylglycerol lipase in blood serum http://purl.obolibrary.org/obo/OBA_2042948 GCST90234466 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily A member 2 level in Chronic kidney disease with hypertension and no diabetes (15614_168) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily A member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042195 GCST90234467 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 5 level in Chronic kidney disease with hypertension and no diabetes (21883_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040206 GCST90235907 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleolysin TIA-1 isoform p40 level in Chronic kidney disease with hypertension and no diabetes (21885_196) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytotoxic granule associated RNA binding protein TIA1 in blood serum http://purl.obolibrary.org/obo/OBA_2044367 GCST90235908 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cerebellin-2 level in Chronic kidney disease with hypertension and no diabetes (21887_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cerebellin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040914 GCST90235909 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C7orf24 level in Chronic kidney disease with hypertension and no diabetes (21889_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-glutamylcyclotransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041709 GCST90235910 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibulin-7 level in Chronic kidney disease with hypertension and no diabetes (21891_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of fibulin-7 in blood serum http://purl.obolibrary.org/obo/OBA_2041554 GCST90235911 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon lambda-4 level in Chronic kidney disease with hypertension and no diabetes (21895_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interferon lambda-4 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044894 GCST90235912 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IL-17/ IL-17F level in Chronic kidney disease with hypertension and no diabetes (21897_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235913 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. inhibin A level in Chronic kidney disease with hypertension and no diabetes (21899_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 inhibin beta A chain measurement http://www.ebi.ac.uk/efo/EFO_0020469 GCST90235914 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha L beta 2 level in Chronic kidney disease with hypertension and no diabetes (21903_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235915 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-2/ b1 level in Chronic kidney disease with hypertension and no diabetes (21905_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235916 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin a5b1 level in Chronic kidney disease with hypertension and no diabetes (21909_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235917 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin a5b1 level in Chronic kidney disease with hypertension and no diabetes (21909_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235918 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation Factor XI level in Chronic kidney disease with hypertension and no diabetes (2190_55) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of coagulation factor XI in blood serum http://purl.obolibrary.org/obo/OBA_2041532 GCST90235919 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Norrin level in Chronic kidney disease with hypertension and no diabetes (21911_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of norrin in blood serum http://purl.obolibrary.org/obo/OBA_2042535 GCST90235920 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor YY2 level in Chronic kidney disease with hypertension and no diabetes (21913_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor YY2 in blood serum http://purl.obolibrary.org/obo/OBA_2044169 GCST90235921 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. OTU domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (21915_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of OTU domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044507 GCST90235922 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin thioesterase otulin level in Chronic kidney disease with hypertension and no diabetes (21916_82) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ubiquitin thioesterase otulin in blood serum http://purl.obolibrary.org/obo/OBA_2044547 GCST90235923 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SAE1/ SAE2 level in Chronic kidney disease with hypertension and no diabetes (21923_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235924 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming growth factor beta-1 level in Chronic kidney disease with hypertension and no diabetes (21925_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 transforming growth factor beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020780 GCST90235925 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 27 level in Chronic kidney disease with hypertension and no diabetes (2192_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 27 measurement http://www.ebi.ac.uk/efo/EFO_0020198 GCST90235926 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UB2L3/ PolyUbiquitin K48 level in Chronic kidney disease with hypertension and no diabetes (21931_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235927 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like modifier-activating enzyme 7 level in Chronic kidney disease with hypertension and no diabetes (21933_7) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of ubiquitin-like modifier-activating enzyme 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043984 GCST90235928 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 H level in Chronic kidney disease with hypertension and no diabetes (21935_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 H in blood serum http://purl.obolibrary.org/obo/OBA_2043996 GCST90235929 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ULA1/ UBA3 level in Chronic kidney disease with hypertension and no diabetes (21939_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235930 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-10b level in Chronic kidney disease with hypertension and no diabetes (21940_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein Wnt-10b in blood serum http://purl.obolibrary.org/obo/OBA_2044138 GCST90235931 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-16 level in Chronic kidney disease with hypertension and no diabetes (21942_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Wnt-16 in blood serum http://purl.obolibrary.org/obo/OBA_2044140 GCST90235932 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-16 level in Chronic kidney disease with hypertension and no diabetes (21943_170) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Wnt-16 in blood serum http://purl.obolibrary.org/obo/OBA_2044140 GCST90235933 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-5b level in Chronic kidney disease with hypertension and no diabetes (21945_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Wnt-5b in blood serum http://purl.obolibrary.org/obo/OBA_2044142 GCST90235934 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IL-6/ IL-6 sRa Complex level in Chronic kidney disease with hypertension and no diabetes (21946_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235935 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 precursor protein-binding family B member 1-interacting protein level in Chronic kidney disease with hypertension and no diabetes (21949_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of amyloid beta A4 precursor protein-binding family B member 1-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2040614 GCST90235936 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aryl hydrocarbon receptor nuclear translocator level in Chronic kidney disease with hypertension and no diabetes (21951_32) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of aryl hydrocarbon receptor nuclear translocator in blood serum http://purl.obolibrary.org/obo/OBA_2040680 GCST90235937 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Large proline-rich protein BAT3 level in Chronic kidney disease with hypertension and no diabetes (21955_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of large proline-rich protein BAT3 in blood serum http://purl.obolibrary.org/obo/OBA_2040780 GCST90235938 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoinositide 3-kinase adapter protein 1 level in Chronic kidney disease with hypertension and no diabetes (21957_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoinositide 3-kinase adapter protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042887 GCST90235939 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Active breakpoint cluster region-related protein level in Chronic kidney disease with hypertension and no diabetes (21958_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of active breakpoint cluster region-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2040465 GCST90235940 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD2-associated protein level in Chronic kidney disease with hypertension and no diabetes (21961_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD2-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2040941 GCST90235941 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disabled homolog 2 level in Chronic kidney disease with hypertension and no diabetes (21963_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disabled homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041224 GCST90235942 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BEX2 level in Chronic kidney disease with hypertension and no diabetes (22082_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BEX2 in blood serum http://purl.obolibrary.org/obo/OBA_2040794 GCST90235993 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BEX5 level in Chronic kidney disease with hypertension and no diabetes (22083_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BEX5 in blood serum http://purl.obolibrary.org/obo/OBA_2040796 GCST90235994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polycomb complex protein BMI-1 level in Chronic kidney disease with hypertension and no diabetes (22085_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Polycomb complex protein BMI-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040811 GCST90235995 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Breast cancer metastasis-suppressor 1-like protein level in Chronic kidney disease with hypertension and no diabetes (22086_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of breast cancer metastasis-suppressor 1-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2040827 GCST90235996 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BTG1 level in Chronic kidney disease with hypertension and no diabetes (22088_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BTG1 in blood serum http://purl.obolibrary.org/obo/OBA_2040832 GCST90235997 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BTG4 level in Chronic kidney disease with hypertension and no diabetes (22089_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BTG4 in blood serum http://purl.obolibrary.org/obo/OBA_2040834 GCST90235998 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-ureidopropionase level in Chronic kidney disease with hypertension and no diabetes (22091_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of beta-ureidopropionase in blood serum http://purl.obolibrary.org/obo/OBA_2044041 GCST90235999 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-4 level in Chronic kidney disease with hypertension and no diabetes (22092_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caspase-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040407 GCST90236000 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C2orf73 level in Chronic kidney disease with hypertension and no diabetes (22094_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C2orf73 in blood serum http://purl.obolibrary.org/obo/OBA_2044842 GCST90236001 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromobox protein homolog 2 level in Chronic kidney disease with hypertension and no diabetes (22095_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromobox protein homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040921 GCST90236002 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease 27 level in Chronic kidney disease with hypertension and no diabetes (3624_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine protease 27 measurement http://www.ebi.ac.uk/efo/EFO_0008280 GCST90237450 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane metallo-endopeptidase-like 1 level in Chronic kidney disease with hypertension and no diabetes (3627_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 membrane metallo-endopeptidase-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020564 GCST90237451 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity mitogen-activated protein kinase kinase 2 level in Chronic kidney disease with hypertension and no diabetes (3628_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 dual specificity mitogen-activated protein kinase kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008112 GCST90237452 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase MRCK beta level in Chronic kidney disease with hypertension and no diabetes (3629_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase MRCK beta measurement http://www.ebi.ac.uk/efo/EFO_0020727 GCST90237453 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell adhesion molecule 3 level in Chronic kidney disease with hypertension and no diabetes (3630_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 cell adhesion molecule 3 measurement http://www.ebi.ac.uk/efo/EFO_0020252 GCST90237454 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nidogen-2 level in Chronic kidney disease with hypertension and no diabetes (3633_70) 466 African American individuals NA Illumina [14870897] (imputed) 1 nidogen-2 measurement http://www.ebi.ac.uk/efo/EFO_0020608 GCST90237455 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Opioid-binding protein/cell adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (3634_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 opioid-binding protein/cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020618 GCST90237456 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. OCIA domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (3635_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 OCIA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008252 GCST90237457 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxidized low-density lipoprotein receptor 1 level in Chronic kidney disease with hypertension and no diabetes (3636_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 oxidized low-density lipoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020620 GCST90237458 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. alpha-2-macroglobulin receptor-associated protein level in Chronic kidney disease with hypertension and no diabetes (3640_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 alpha-2-macroglobulin receptor-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0008021 GCST90237459 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLAM family member 5 level in Chronic kidney disease with hypertension and no diabetes (3642_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90237460 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dickkopf-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (3644_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 dickkopf-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020324 GCST90237461 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 4:Lymphocyte antigen 96 complex level in Chronic kidney disease with hypertension and no diabetes (3647_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 toll-like receptor 4:Lymphocyte antigen 96 complex measurement http://www.ebi.ac.uk/efo/EFO_0008301 GCST90237462 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor receptor 2 level in Chronic kidney disease with hypertension and no diabetes (3651_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 vascular endothelial growth factor receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008314 GCST90237463 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BMP-binding endothelial regulator protein level in Chronic kidney disease with hypertension and no diabetes (3654_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 BMP-binding endothelial regulator protein measurement http://www.ebi.ac.uk/efo/EFO_0020183 GCST90237464 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H-related protein 5 level in Chronic kidney disease with hypertension and no diabetes (3666_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement factor H-related protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0008098 GCST90237465 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cation-independent mannose-6-phosphate receptor level in Chronic kidney disease with hypertension and no diabetes (3676_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 cation-independent mannose-6-phosphate receptor measurement http://www.ebi.ac.uk/efo/EFO_0008075 GCST90237466 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-14 level in Chronic kidney disease with hypertension and no diabetes (3681_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-14 measurement http://www.ebi.ac.uk/efo/EFO_0020513 GCST90237467 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage scavenger receptor types I and II level in Chronic kidney disease with hypertension and no diabetes (3684_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90237468 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane frizzled-related protein level in Chronic kidney disease with hypertension and no diabetes (3685_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 membrane frizzled-related protein measurement http://www.ebi.ac.uk/efo/EFO_0020563 GCST90237469 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-2-macroglobulin level in Chronic kidney disease with hypertension and no diabetes (3708_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-2-macroglobulin measurement http://www.ebi.ac.uk/efo/EFO_0020138 GCST90237470 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alanine aminotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (3709_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 serum alanine aminotransferase measurement http://www.ebi.ac.uk/efo/EFO_0004735 GCST90237471 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiostatin level in Chronic kidney disease with hypertension and no diabetes (3710_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiostatin measurement http://www.ebi.ac.uk/efo/EFO_0008024 GCST90237472 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Creatine kinase M-type:Creatine kinase B-type heterodimer level in Chronic kidney disease with hypertension and no diabetes (3714_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 creatine kinase m-type:creatine kinase b-type heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020292 GCST90237473 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase inhibitor 1B level in Chronic kidney disease with hypertension and no diabetes (3719_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 cyclin-dependent kinase inhibitor 1b measurement http://www.ebi.ac.uk/efo/EFO_0020298 GCST90237474 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brain natriuretic peptide 32 level in Chronic kidney disease with hypertension and no diabetes (3723_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 brain natriuretic peptide 32 measurement http://www.ebi.ac.uk/efo/EFO_0020191 GCST90237475 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptide YY level in Chronic kidney disease with hypertension and no diabetes (3727_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptide yy measurement http://www.ebi.ac.uk/efo/EFO_0020623 GCST90237476 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretin level in Chronic kidney disease with hypertension and no diabetes (3728_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 secretin measurement http://www.ebi.ac.uk/efo/EFO_0020719 GCST90237477 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 4 level in Chronic kidney disease with hypertension and no diabetes (3730_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 4 measurement http://www.ebi.ac.uk/efo/EFO_0020814 GCST90237478 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 6 level in Chronic kidney disease with hypertension and no diabetes (3736_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90237479 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage colony-stimulating factor 1 level in Chronic kidney disease with hypertension and no diabetes (3738_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage colony-stimulating factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020546 GCST90237480 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-IIb: beta-3 complex level in Chronic kidney disease with hypertension and no diabetes (3739_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-IIb: beta-3 complex measurement http://www.ebi.ac.uk/efo/EFO_0020479 GCST90237481 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-5 level in Chronic kidney disease with hypertension and no diabetes (3741_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2040292 GCST90237482 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activated Protein C level in Chronic kidney disease with hypertension and no diabetes (3758_63) 466 African American individuals NA Illumina [14870897] (imputed) 1 activated protein C measurement http://www.ebi.ac.uk/efo/EFO_0020126 GCST90237483 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin G/H synthase 2 level in Chronic kidney disease with hypertension and no diabetes (3761_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 prostaglandin g/h synthase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020659 GCST90237484 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-1A level in Chronic kidney disease with hypertension and no diabetes (3766_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 syntaxin-1a measurement http://www.ebi.ac.uk/efo/EFO_0020759 GCST90237485 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-1 receptor, soluble level in Chronic kidney disease with hypertension and no diabetes (3773_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 angiopoietin-1 receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0008023 GCST90237486 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 9 level in Chronic kidney disease with hypertension and no diabetes (3795_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 disintegrin and metalloproteinase domain-containing protein 9 measurement http://www.ebi.ac.uk/efo/EFO_0020329 GCST90237487 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (3796_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiopoietin-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020149 GCST90237488 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-2 level in Chronic kidney disease with hypertension and no diabetes (3797_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020212 GCST90237489 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. F-box only protein 48 level in Chronic kidney disease with hypertension and no diabetes (22144_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of F-box only protein 48 in blood serum http://purl.obolibrary.org/obo/OBA_2041559 GCST90236028 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fos-related antigen 2 level in Chronic kidney disease with hypertension and no diabetes (22146_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fos-related antigen 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041604 GCST90236029 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein O4 level in Chronic kidney disease with hypertension and no diabetes (22147_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein O4 in blood serum http://purl.obolibrary.org/obo/OBA_2041612 GCST90236030 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein P3 level in Chronic kidney disease with hypertension and no diabetes (22148_135) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein P3 in blood serum http://purl.obolibrary.org/obo/OBA_2040275 GCST90236031 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FUN14 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (22149_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of FUN14 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044300 GCST90236032 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GA-binding protein subunit beta-1 level in Chronic kidney disease with hypertension and no diabetes (22150_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GA-binding protein subunit beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041650 GCST90236033 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein goosecoid-2 level in Chronic kidney disease with hypertension and no diabetes (22151_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein goosecoid-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041796 GCST90236034 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 9 level in Chronic kidney disease with hypertension and no diabetes (22152_162) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 9 in blood serum http://purl.obolibrary.org/obo/OBA_2041667 GCST90236035 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GATA zinc finger domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (22154_37) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of GATA zinc finger domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044301 GCST90236036 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gem-associated protein 7 level in Chronic kidney disease with hypertension and no diabetes (22155_44) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of gem-associated protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041703 GCST90236037 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA-specific adenosine deaminase 1 level in Chronic kidney disease with hypertension and no diabetes (22363_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA-specific adenosine deaminase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040508 GCST90236038 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-dependent transcription factor ATF-5 level in Chronic kidney disease with hypertension and no diabetes (22365_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-dependent transcription factor ATF-5 in blood serum http://purl.obolibrary.org/obo/OBA_2040714 GCST90236039 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0705 protein C11orf49 level in Chronic kidney disease with hypertension and no diabetes (22367_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of centriolar satellite-associated tubulin polyglutamylase complex regulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044874 GCST90236040 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Doublesex- and mab-3-related transcription factor C2 level in Chronic kidney disease with hypertension and no diabetes (22369_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of doublesex- and mab-3-related transcription factor C2 in blood serum http://purl.obolibrary.org/obo/OBA_2041324 GCST90236041 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM110A level in Chronic kidney disease with hypertension and no diabetes (22371_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM110A in blood serum http://purl.obolibrary.org/obo/OBA_2044492 GCST90236042 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hairy/enhancer-of-split related with YRPW motif protein 1 level in Chronic kidney disease with hypertension and no diabetes (22374_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hairy/enhancer-of-split related with YRPW motif protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041868 GCST90236043 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein Hox-A5 level in Chronic kidney disease with hypertension and no diabetes (22376_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein Hox-A5 in blood serum http://purl.obolibrary.org/obo/OBA_2041916 GCST90236044 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immediate early response gene 2 protein level in Chronic kidney disease with hypertension and no diabetes (22377_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immediate early response gene 2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041973 GCST90236045 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin 34 level in Chronic kidney disease with hypertension and no diabetes (22378_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type I cuticular Ha4 in blood serum http://purl.obolibrary.org/obo/OBA_2042143 GCST90236046 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoribonuclease LACTB2 level in Chronic kidney disease with hypertension and no diabetes (22381_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoribonuclease LACTB2 in blood serum http://purl.obolibrary.org/obo/OBA_2042154 GCST90236047 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MITF level in Chronic kidney disease with hypertension and no diabetes (22383_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microphthalmia-associated transcription factor in blood serum http://purl.obolibrary.org/obo/OBA_2042372 GCST90236048 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PWWP domain-containing protein MUM1 level in Chronic kidney disease with hypertension and no diabetes (22385_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PWWP domain-containing DNA repair factor 3A in blood serum http://purl.obolibrary.org/obo/OBA_2042461 GCST90236049 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein OTX1 level in Chronic kidney disease with hypertension and no diabetes (22386_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein OTX1 in blood serum http://purl.obolibrary.org/obo/OBA_2042723 GCST90236050 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pituitary homeobox 3 level in Chronic kidney disease with hypertension and no diabetes (22387_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pituitary homeobox 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042904 GCST90236051 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone deacetylase complex subunit SAP30L level in Chronic kidney disease with hypertension and no diabetes (22391_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone deacetylase complex subunit SAP30L in blood serum http://purl.obolibrary.org/obo/OBA_2043379 GCST90236052 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-Y-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (22098_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-Y-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040936 GCST90236003 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C4orf36 level in Chronic kidney disease with hypertension and no diabetes (22099_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C4orf36 in blood serum http://purl.obolibrary.org/obo/OBA_2044857 GCST90236004 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 20 level in Chronic kidney disease with hypertension and no diabetes (22103_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 20 in blood serum http://purl.obolibrary.org/obo/OBA_2040938 GCST90236005 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein CDX-1 level in Chronic kidney disease with hypertension and no diabetes (22104_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein CDX-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040975 GCST90236006 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22112_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041101 GCST90236007 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquinone biosynthesis monooxygenase COQ6, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22113_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquinone biosynthesis monooxygenase COQ6, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041102 GCST90236008 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C18orf54 level in Chronic kidney disease with hypertension and no diabetes (22114_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lung adenoma susceptibility protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044839 GCST90236009 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-responsive element-binding protein-like 2 level in Chronic kidney disease with hypertension and no diabetes (22115_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-responsive element-binding protein-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041135 GCST90236010 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-responsive element modulator level in Chronic kidney disease with hypertension and no diabetes (22116_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-responsive element modulator in blood serum http://purl.obolibrary.org/obo/OBA_2041138 GCST90236011 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chondrosarcoma-associated gene 2/3 protein level in Chronic kidney disease with hypertension and no diabetes (22118_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chondrosarcoma-associated gene 2/3A protein in blood serum http://purl.obolibrary.org/obo/OBA_2041164 GCST90236012 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COP9 signalosome complex subunit 8 level in Chronic kidney disease with hypertension and no diabetes (22119_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of COP9 signalosome complex subunit 8 in blood serum http://purl.obolibrary.org/obo/OBA_2041099 GCST90236013 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metalloproteinase inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (2211_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 metalloproteinase inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020566 GCST90236014 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DDB1- and CUL4-associated factor 11 level in Chronic kidney disease with hypertension and no diabetes (22120_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of DDB1- and CUL4-associated factor 11 in blood serum http://purl.obolibrary.org/obo/OBA_2044541 GCST90236015 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DDB1- and CUL4-associated factor 12 level in Chronic kidney disease with hypertension and no diabetes (22121_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DDB1- and CUL4-associated factor 12 in blood serum http://purl.obolibrary.org/obo/OBA_2044588 GCST90236016 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein DLX-2 level in Chronic kidney disease with hypertension and no diabetes (22123_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein DLX-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041317 GCST90236017 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dystrotelin level in Chronic kidney disease with hypertension and no diabetes (22124_94) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dystrotelin in blood serum http://purl.obolibrary.org/obo/OBA_2041400 GCST90236018 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E2F5 level in Chronic kidney disease with hypertension and no diabetes (22125_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor E2F5 in blood serum http://purl.obolibrary.org/obo/OBA_2041403 GCST90236019 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ETS domain-containing protein Elk-4 level in Chronic kidney disease with hypertension and no diabetes (22128_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ETS domain-containing protein Elk-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041468 GCST90236020 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA polymerase II elongation factor ELL3 level in Chronic kidney disease with hypertension and no diabetes (22129_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA polymerase II elongation factor ELL3 in blood serum http://purl.obolibrary.org/obo/OBA_2041471 GCST90236021 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tissue-type plasminogen activator level in Chronic kidney disease with hypertension and no diabetes (2212_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 tissue-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0020776 GCST90236022 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclease EXOG, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22136_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclease EXOG, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041476 GCST90236023 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM102B level in Chronic kidney disease with hypertension and no diabetes (22137_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM102B in blood serum http://purl.obolibrary.org/obo/OBA_2044292 GCST90236024 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM204A level in Chronic kidney disease with hypertension and no diabetes (22140_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM204A in blood serum http://purl.obolibrary.org/obo/OBA_2044715 GCST90236025 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (22141_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042851 GCST90236026 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative protein N-methyltransferase FAM86B1 level in Chronic kidney disease with hypertension and no diabetes (22142_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of putative protein N-methyltransferase FAM86B1 in blood serum http://purl.obolibrary.org/obo/OBA_2044650 GCST90236027 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaredoxin-related protein 5, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (16597_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutaredoxin-related protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041735 GCST90234539 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GPN-loop GTPase 1 level in Chronic kidney disease with hypertension and no diabetes (16599_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GPN-loop GTPase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041773 GCST90234540 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q and tumor necrosis factor-related protein 9A level in Chronic kidney disease with hypertension and no diabetes (16605_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of complement C1q and tumor necrosis factor-related protein 9A in blood serum http://purl.obolibrary.org/obo/OBA_2040853 GCST90234541 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldose reductase level in Chronic kidney disease with hypertension and no diabetes (16606_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member B1 in blood serum http://purl.obolibrary.org/obo/OBA_2040547 GCST90234542 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gelsolin level in Chronic kidney disease with hypertension and no diabetes (16607_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 gelsolin measurement http://www.ebi.ac.uk/efo/EFO_0020402 GCST90234543 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kin of IRRE-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (16609_106) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kin of IRRE-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042111 GCST90234544 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 10 level in Chronic kidney disease with hypertension and no diabetes (16610_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor-related protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042228 GCST90234545 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-17 level in Chronic kidney disease with hypertension and no diabetes (16613_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cadherin-17 in blood serum http://purl.obolibrary.org/obo/OBA_2040959 GCST90234546 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. R-spondin-1 level in Chronic kidney disease with hypertension and no diabetes (16614_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of R-spondin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043350 GCST90234547 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-enolase level in Chronic kidney disease with hypertension and no diabetes (16616_137) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-enolase in blood serum http://purl.obolibrary.org/obo/OBA_2041478 GCST90234548 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Early activation antigen CD69 level in Chronic kidney disease with hypertension and no diabetes (16618_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD69 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040272 GCST90234549 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte antigen 75 level in Chronic kidney disease with hypertension and no diabetes (16620_26) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lymphocyte antigen 75 isoform 4 and LY75-CD302 fusion isoforms V34-2/V33-2 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044895 GCST90234550 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD(P)H-hydrate epimerase level in Chronic kidney disease with hypertension and no diabetes (16621_77) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of apolipoprotein A-I-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2040621 GCST90234551 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activin B level in Chronic kidney disease with hypertension and no diabetes (16746_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activin/inhibin beta B chain in blood serum http://purl.obolibrary.org/obo/OBA_2040210 GCST90234552 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 3 level in Chronic kidney disease with hypertension and no diabetes (16748_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040813 GCST90234553 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 10 level in Chronic kidney disease with hypertension and no diabetes (16749_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 3B in blood serum http://purl.obolibrary.org/obo/OBA_2041697 GCST90234554 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Natriuretic peptides B level in Chronic kidney disease with hypertension and no diabetes (16751_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 natriuretic peptides B measurement http://www.ebi.ac.uk/efo/EFO_0010628 GCST90234555 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-2(VI) chain level in Chronic kidney disease with hypertension and no diabetes (16753_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-2(VI) chain in blood serum http://purl.obolibrary.org/obo/OBA_2040439 GCST90234556 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peripheral plasma membrane protein CASK level in Chronic kidney disease with hypertension and no diabetes (16754_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peripheral plasma membrane protein CASK in blood serum http://purl.obolibrary.org/obo/OBA_2040904 GCST90234557 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 3 level in Chronic kidney disease with hypertension and no diabetes (16755_195) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth/differentiation factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041698 GCST90234558 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 7 level in Chronic kidney disease with hypertension and no diabetes (16756_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth/differentiation factor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040212 GCST90234559 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatoma-derived growth factor level in Chronic kidney disease with hypertension and no diabetes (16758_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatoma-derived growth factor in blood serum http://purl.obolibrary.org/obo/OBA_2041849 GCST90234560 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-26 level in Chronic kidney disease with hypertension and no diabetes (16760_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-26 in blood serum http://purl.obolibrary.org/obo/OBA_2040304 GCST90234561 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte cell-derived chemotaxin-2 level in Chronic kidney disease with hypertension and no diabetes (16763_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte cell-derived chemotaxin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042187 GCST90234562 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet basic protein level in Chronic kidney disease with hypertension and no diabetes (16765_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of platelet basic protein in blood serum http://purl.obolibrary.org/obo/OBA_2042981 GCST90234563 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IQ domain-containing protein D level in Chronic kidney disease with hypertension and no diabetes (22481_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynein regulatory complex protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044498 GCST90236078 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type I cytoskeletal 14 level in Chronic kidney disease with hypertension and no diabetes (22482_87) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of keratin, type I cytoskeletal 14 in blood serum http://purl.obolibrary.org/obo/OBA_2042138 GCST90236079 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type II cytoskeletal 71 level in Chronic kidney disease with hypertension and no diabetes (22483_109) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type II cytoskeletal 71 in blood serum http://purl.obolibrary.org/obo/OBA_2042147 GCST90236080 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase I isoform alpha-like level in Chronic kidney disease with hypertension and no diabetes (22484_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of casein kinase I isoform alpha-like in blood serum http://purl.obolibrary.org/obo/OBA_2041169 GCST90236081 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD7 level in Chronic kidney disease with hypertension and no diabetes (22485_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD7 in blood serum http://purl.obolibrary.org/obo/OBA_2044321 GCST90236082 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type II cytoskeletal 6A level in Chronic kidney disease with hypertension and no diabetes (22486_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type II cytoskeletal 6A in blood serum http://purl.obolibrary.org/obo/OBA_2042145 GCST90236083 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Krueppel-like factor 9 level in Chronic kidney disease with hypertension and no diabetes (22488_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of krueppel-like factor 9 in blood serum http://purl.obolibrary.org/obo/OBA_2042119 GCST90236084 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lipocalin-like 1 protein level in Chronic kidney disease with hypertension and no diabetes (22490_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lipocalin-like 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042175 GCST90236085 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (22491_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LIM domain-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042180 GCST90236086 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain only protein 3 level in Chronic kidney disease with hypertension and no diabetes (22492_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LIM domain only protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044748 GCST90236087 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LYR motif-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (22496_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LYR motif-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042252 GCST90236088 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mediator of RNA polymerase II transcription subunit 28 level in Chronic kidney disease with hypertension and no diabetes (22499_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mediator of RNA polymerase II transcription subunit 28 in blood serum http://purl.obolibrary.org/obo/OBA_2042328 GCST90236089 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mediator of RNA polymerase II transcription subunit 11 level in Chronic kidney disease with hypertension and no diabetes (22500_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mediator of RNA polymerase II transcription subunit 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042326 GCST90236090 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein Mohawk level in Chronic kidney disease with hypertension and no diabetes (22503_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein Mohawk in blood serum http://purl.obolibrary.org/obo/OBA_2042374 GCST90236091 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD4-binding protein 2-like 2 level in Chronic kidney disease with hypertension and no diabetes (22504_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD4-binding protein 2-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042493 GCST90236092 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD kinase 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22505_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NAD kinase 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044244 GCST90236093 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetyltransferase 5 level in Chronic kidney disease with hypertension and no diabetes (22506_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-alpha-acetyltransferase 20 in blood serum http://purl.obolibrary.org/obo/OBA_2042517 GCST90236094 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (22508_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042543 GCST90236095 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arginine-hydroxylase NDUFAF5, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22509_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of arginine-hydroxylase NDUFAF5, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044792 GCST90236096 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear factor erythroid 2-related factor 2 level in Chronic kidney disease with hypertension and no diabetes (22510_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear factor erythroid 2-related factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042571 GCST90236097 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear transcription factor Y subunit alpha level in Chronic kidney disease with hypertension and no diabetes (22511_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear transcription factor Y subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042575 GCST90236098 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epithelial discoidin domain-containing receptor 1 level in Chronic kidney disease with hypertension and no diabetes (4122_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 epithelial discoidin domain-containing receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020362 GCST90237548 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 4 level in Chronic kidney disease with hypertension and no diabetes (4123_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 4 measurement http://www.ebi.ac.uk/efo/EFO_0020382 GCST90237549 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (4124_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90237550 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Advanced glycosylation end product-specific receptor, soluble level in Chronic kidney disease with hypertension and no diabetes (4125_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 advanced glycosylation end product-specific receptor, soluble measurement http://www.ebi.ac.uk/efo/EFO_0020131 GCST90237551 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SERTA domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (22392_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SERTA domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043467 GCST90236053 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyroid transcription factor 1-associated protein 26 level in Chronic kidney disease with hypertension and no diabetes (22393_130) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thyroid transcription factor 1-associated protein 26 in blood serum http://purl.obolibrary.org/obo/OBA_2040928 GCST90236054 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor 21 level in Chronic kidney disease with hypertension and no diabetes (22394_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor 21 in blood serum http://purl.obolibrary.org/obo/OBA_2043811 GCST90236055 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tristetraproline level in Chronic kidney disease with hypertension and no diabetes (22395_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mRNA decay activator protein ZFP36 in blood serum http://purl.obolibrary.org/obo/OBA_2044181 GCST90236056 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. X-box-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (22397_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of X-box-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044148 GCST90236057 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acidic leucine-rich nuclear phosphoprotein 32 family member C level in Chronic kidney disease with hypertension and no diabetes (22398_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acidic leucine-rich nuclear phosphoprotein 32 family member C in blood serum http://purl.obolibrary.org/obo/OBA_2044770 GCST90236058 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylyl cyclase-activating protein 2 level in Chronic kidney disease with hypertension and no diabetes (22401_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanylyl cyclase-activating protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041821 GCST90236059 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H2A type 1-A level in Chronic kidney disease with hypertension and no diabetes (22402_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone H2A type 1-A in blood serum http://purl.obolibrary.org/obo/OBA_2041879 GCST90236060 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol hexakisphosphate kinase 1 level in Chronic kidney disease with hypertension and no diabetes (22404_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol hexakisphosphate kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042040 GCST90236061 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoenolpyruvate carboxykinase [GTP], mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22405_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoenolpyruvate carboxykinase [GTP], mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042800 GCST90236062 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase tousled-like 1 level in Chronic kidney disease with hypertension and no diabetes (22414_127) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase tousled-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043863 GCST90236063 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase CBL-C level in Chronic kidney disease with hypertension and no diabetes (22417_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase CBL-C in blood serum http://purl.obolibrary.org/obo/OBA_2040912 GCST90236064 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase pellino homolog 1 level in Chronic kidney disease with hypertension and no diabetes (22421_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase pellino homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040417 GCST90236065 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysine-specific histone demethylase 1A level in Chronic kidney disease with hypertension and no diabetes (22429_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysine-specific histone demethylase 1A in blood serum http://purl.obolibrary.org/obo/OBA_2040607 GCST90236066 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-chimaerin level in Chronic kidney disease with hypertension and no diabetes (22430_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-chimaerin in blood serum http://purl.obolibrary.org/obo/OBA_2041014 GCST90236067 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum response factor-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (22431_164) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serum response factor-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043651 GCST90236068 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-binding protein 5 level in Chronic kidney disease with hypertension and no diabetes (22445_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-binding protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040866 GCST90236069 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor HES-1 level in Chronic kidney disease with hypertension and no diabetes (22465_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor HES-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041860 GCST90236070 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor HES-5 level in Chronic kidney disease with hypertension and no diabetes (22466_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor HES-5 in blood serum http://purl.obolibrary.org/obo/OBA_2041862 GCST90236071 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HERV-H LTR-associating protein 3 level in Chronic kidney disease with hypertension and no diabetes (22467_94) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of HERV-H LTR-associating protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041873 GCST90236072 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein HMX2 level in Chronic kidney disease with hypertension and no diabetes (22469_103) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein HMX2 in blood serum http://purl.obolibrary.org/obo/OBA_2041896 GCST90236073 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein Hox-C11 level in Chronic kidney disease with hypertension and no diabetes (22474_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of homeobox protein Hox-C11 in blood serum http://purl.obolibrary.org/obo/OBA_2041917 GCST90236074 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein Hox-D4 level in Chronic kidney disease with hypertension and no diabetes (22476_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein Hox-D4 in blood serum http://purl.obolibrary.org/obo/OBA_2041918 GCST90236075 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol hexakisphosphate kinase 2 level in Chronic kidney disease with hypertension and no diabetes (22479_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol hexakisphosphate kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042041 GCST90236076 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prokineticin-1 level in Chronic kidney disease with hypertension and no diabetes (2247_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 prokineticin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020655 GCST90236077 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 1 member B level in Chronic kidney disease with hypertension and no diabetes (4332_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-type lectin domain family 1 member B measurement http://www.ebi.ac.uk/efo/EFO_0020200 GCST90237627 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum amyloid A-1 protein level in Chronic kidney disease with hypertension and no diabetes (4336_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 serum amyloid A-1 protein measurement http://www.ebi.ac.uk/efo/EFO_0008282 GCST90237628 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-reactive protein level in Chronic kidney disease with hypertension and no diabetes (4337_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-reactive protein measurement http://www.ebi.ac.uk/efo/EFO_0004458 GCST90237629 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 1 level in Chronic kidney disease with hypertension and no diabetes (4342_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 ICAM-1 measurement http://www.ebi.ac.uk/efo/EFO_0004520 GCST90237630 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin beta A chain:Inhibin beta B chain heterodimer level in Chronic kidney disease with hypertension and no diabetes (4383_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 inhibin beta A chain:inhibin beta B chain heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020470 GCST90237631 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 12 level in Chronic kidney disease with hypertension and no diabetes (4392_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 12 measurement http://www.ebi.ac.uk/efo/EFO_0020377 GCST90237632 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 16 level in Chronic kidney disease with hypertension and no diabetes (4393_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 16 measurement http://www.ebi.ac.uk/efo/EFO_0020378 GCST90237633 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 8 isoform A level in Chronic kidney disease with hypertension and no diabetes (4394_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor 8 in blood serum http://purl.obolibrary.org/obo/OBA_2041575 GCST90237634 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon lambda-1 level in Chronic kidney disease with hypertension and no diabetes (4396_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon lambda-1 measurement http://www.ebi.ac.uk/efo/EFO_0020485 GCST90237635 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon lambda-2 level in Chronic kidney disease with hypertension and no diabetes (4397_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon lambda-2 measurement http://www.ebi.ac.uk/efo/EFO_0020486 GCST90237636 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte growth factor-like protein level in Chronic kidney disease with hypertension and no diabetes (4407_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 hepatocyte growth factor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0008154 GCST90237637 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Antileukoproteinase level in Chronic kidney disease with hypertension and no diabetes (4413_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 antileukoproteinase measurement http://www.ebi.ac.uk/efo/EFO_0020154 GCST90237638 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pulmonary surfactant-associated protein D level in Chronic kidney disease with hypertension and no diabetes (4414_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90237639 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 12 level in Chronic kidney disease with hypertension and no diabetes (4420_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 disintegrin and metalloproteinase domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0020328 GCST90237640 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bcl-2-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (4423_77) 466 African American individuals NA Illumina [14870897] (imputed) 1 BCL-2-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020177 GCST90237641 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 2 level in Chronic kidney disease with hypertension and no diabetes (4428_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbohydrate sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020225 GCST90237642 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 6 level in Chronic kidney disease with hypertension and no diabetes (4429_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbohydrate sulfotransferase 6 measurement http://www.ebi.ac.uk/efo/EFO_0020226 GCST90237643 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collectin-11 level in Chronic kidney disease with hypertension and no diabetes (4430_44) 466 African American individuals NA Illumina [14870897] (imputed) 1 collectin-11 measurement http://www.ebi.ac.uk/efo/EFO_0008088 GCST90237644 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mucosal addressin cell adhesion molecule 1 level in Chronic kidney disease with hypertension and no diabetes (11258_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mucosal addressin cell adhesion molecule 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042260 GCST90233154 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SUN domain-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (11260_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SUN domain-containing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043612 GCST90233155 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TraB domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (11262_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TraB domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2044796 GCST90233156 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calsequestrin-1 level in Chronic kidney disease with hypertension and no diabetes (11263_57) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of calsequestrin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040905 GCST90233157 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Xanthine dehydrogenase/oxidase level in Chronic kidney disease with hypertension and no diabetes (11264_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of xanthine dehydrogenase/oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2044149 GCST90233158 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinal dehydrogenase 1 level in Chronic kidney disease with hypertension and no diabetes (11265_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldehyde dehydrogenase 1A1 in blood serum http://purl.obolibrary.org/obo/OBA_2040558 GCST90233159 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. P-selectin glycoprotein ligand 1 level in Chronic kidney disease with hypertension and no diabetes (11266_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 P-selectin glycoprotein ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0010922 GCST90233160 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombin level in Chronic kidney disease with hypertension and no diabetes (4157_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 thrombin measurement http://www.ebi.ac.uk/efo/EFO_0020768 GCST90237577 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urokinase-type plasminogen activator level in Chronic kidney disease with hypertension and no diabetes (4158_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 urokinase-type plasminogen activator measurement http://www.ebi.ac.uk/efo/EFO_0010803 GCST90237578 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H level in Chronic kidney disease with hypertension and no diabetes (4159_130) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement factor H measurement http://www.ebi.ac.uk/efo/EFO_0008097 GCST90237579 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 72 kDa type IV collagenase level in Chronic kidney disease with hypertension and no diabetes (4160_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 72 kda type IV collagenase measurement http://www.ebi.ac.uk/efo/EFO_0020122 GCST90237580 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serotransferrin level in Chronic kidney disease with hypertension and no diabetes (4162_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 serotransferrin measurement http://www.ebi.ac.uk/efo/EFO_0020735 GCST90237581 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H2A.z level in Chronic kidney disease with hypertension and no diabetes (4163_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone H2A.Z measurement http://www.ebi.ac.uk/efo/EFO_0020454 GCST90237582 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein gamma level in Chronic kidney disease with hypertension and no diabetes (4179_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 14-3-3 protein gamma in blood serum http://purl.obolibrary.org/obo/OBA_2044166 GCST90237583 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4E-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (4184_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 eukaryotic translation initiation factor 4E-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020368 GCST90237584 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 6-phosphogluconate dehydrogenase, decarboxylating level in Chronic kidney disease with hypertension and no diabetes (4187_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 6-phosphogluconate dehydrogenase, decarboxylating measurement http://www.ebi.ac.uk/efo/EFO_0020120 GCST90237585 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aflatoxin B1 aldehyde reductase member 2 level in Chronic kidney disease with hypertension and no diabetes (4188_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 aflatoxin B1 aldehyde reductase member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020132 GCST90237586 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase [NADP(+)] level in Chronic kidney disease with hypertension and no diabetes (4192_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member A1 in blood serum http://purl.obolibrary.org/obo/OBA_2040546 GCST90237587 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acidic leucine-rich nuclear phosphoprotein 32 family member B level in Chronic kidney disease with hypertension and no diabetes (4194_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 acidic leucine-rich nuclear phosphoprotein 32 family member b measurement http://www.ebi.ac.uk/efo/EFO_0020125 GCST90237588 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cofilin-1 level in Chronic kidney disease with hypertension and no diabetes (4203_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 cofilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020267 GCST90237589 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein sorting-associated protein VTA1 homolog level in Chronic kidney disease with hypertension and no diabetes (4209_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 vacuolar protein sorting-associated protein VTA1 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020845 GCST90237590 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor receptor substrate 15-like 1 level in Chronic kidney disease with hypertension and no diabetes (4212_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 epidermal growth factor receptor substrate 15-like 1 measurement http://www.ebi.ac.uk/efo/EFO_0020360 GCST90237591 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-hydroxyacyl-CoA dehydrogenase type-2 level in Chronic kidney disease with hypertension and no diabetes (4217_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 3-hydroxyacyl-coa dehydrogenase type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020114 GCST90237592 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase Fer level in Chronic kidney disease with hypertension and no diabetes (4220_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase FER measurement http://www.ebi.ac.uk/efo/EFO_0020821 GCST90237593 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4 gamma 2 level in Chronic kidney disease with hypertension and no diabetes (4230_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 eukaryotic translation initiation factor 4 gamma 2 measurement http://www.ebi.ac.uk/efo/EFO_0020367 GCST90237594 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor 1 receptor level in Chronic kidney disease with hypertension and no diabetes (4232_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor 1 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020473 GCST90237595 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor-like 1 level in Chronic kidney disease with hypertension and no diabetes (4234_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 GCST90237596 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine carboxyl methyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (4237_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine carboxyl methyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008207 GCST90237597 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein lin-7 homolog B level in Chronic kidney disease with hypertension and no diabetes (4238_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein lin-7 homolog B measurement http://www.ebi.ac.uk/efo/EFO_0021978 GCST90237598 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyruvate kinase PKM level in Chronic kidney disease with hypertension and no diabetes (4240_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 pyruvate kinase pkm measurement http://www.ebi.ac.uk/efo/EFO_0020695 GCST90237599 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase Mdm2 level in Chronic kidney disease with hypertension and no diabetes (4245_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 e3 ubiquitin-protein ligase mdm2 measurement http://www.ebi.ac.uk/efo/EFO_0020340 GCST90237600 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleoside diphosphate kinase B level in Chronic kidney disease with hypertension and no diabetes (4249_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 nucleoside diphosphate kinase B measurement http://www.ebi.ac.uk/efo/EFO_0020615 GCST90237601 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bactericidal permeability-increasing protein level in Chronic kidney disease with hypertension and no diabetes (4126_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 bactericidal permeability-increasing protein measurement http://www.ebi.ac.uk/efo/EFO_0020172 GCST90237552 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C6 level in Chronic kidney disease with hypertension and no diabetes (4127_75) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement component C6 measurement http://www.ebi.ac.uk/efo/EFO_0020281 GCST90237553 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 24 level in Chronic kidney disease with hypertension and no diabetes (4128_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 24 measurement http://www.ebi.ac.uk/efo/EFO_0020197 GCST90237554 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor B level in Chronic kidney disease with hypertension and no diabetes (4129_72) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement factor B measurement http://www.ebi.ac.uk/efo/EFO_0008096 GCST90237555 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 6 level in Chronic kidney disease with hypertension and no diabetes (4130_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020383 GCST90237556 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follistatin level in Chronic kidney disease with hypertension and no diabetes (4132_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 follistatin measurement http://www.ebi.ac.uk/efo/EFO_0010614 GCST90237557 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17D level in Chronic kidney disease with hypertension and no diabetes (4136_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17D measurement http://www.ebi.ac.uk/efo/EFO_0021976 GCST90237558 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-25 level in Chronic kidney disease with hypertension and no diabetes (4137_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-25 in blood serum http://purl.obolibrary.org/obo/OBA_2040244 GCST90237559 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-20 level in Chronic kidney disease with hypertension and no diabetes (4138_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-20 measurement http://www.ebi.ac.uk/efo/EFO_0020496 GCST90237560 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-6 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (4139_71) 466 African American individuals NA Illumina [14870897] (imputed) 1 interleukin 6 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008187 GCST90237561 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-7 level in Chronic kidney disease with hypertension and no diabetes (4140_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-7 in blood serum http://purl.obolibrary.org/obo/OBA_2040264 GCST90237562 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 10 level in Chronic kidney disease with hypertension and no diabetes (4141_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-X-C motif chemokine 10 measurement http://www.ebi.ac.uk/efo/EFO_0008056 GCST90237563 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphotactin level in Chronic kidney disease with hypertension and no diabetes (4143_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphotactin measurement http://www.ebi.ac.uk/efo/EFO_0008214 GCST90237564 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 13 level in Chronic kidney disease with hypertension and no diabetes (4144_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 13 measurement http://www.ebi.ac.uk/efo/EFO_0020195 GCST90237565 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurotrophin-3 level in Chronic kidney disease with hypertension and no diabetes (4145_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurotrophin-3 measurement http://www.ebi.ac.uk/efo/EFO_0010791 GCST90237566 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurotrophin-4 level in Chronic kidney disease with hypertension and no diabetes (4146_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurotrophin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020604 GCST90237567 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pappalysin-1 level in Chronic kidney disease with hypertension and no diabetes (4148_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 pappalysin‐1 measurement http://www.ebi.ac.uk/efo/EFO_0010618 GCST90237568 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor subunit B level in Chronic kidney disease with hypertension and no diabetes (4149_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet-derived growth factor subunit b measurement http://www.ebi.ac.uk/efo/EFO_0020650 GCST90237569 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plasmin level in Chronic kidney disease with hypertension and no diabetes (4150_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 plasmin measurement http://www.ebi.ac.uk/efo/EFO_0020643 GCST90237570 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plasminogen level in Chronic kidney disease with hypertension and no diabetes (4151_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 plasma plasminogen measurement http://www.ebi.ac.uk/efo/EFO_0006309 GCST90237571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plasma kallikrein level in Chronic kidney disease with hypertension and no diabetes (4152_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 plasma kallikrein measurement http://www.ebi.ac.uk/efo/EFO_0008260 GCST90237572 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1-antichymotrypsin complex level in Chronic kidney disease with hypertension and no diabetes (4153_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-1-antichymotrypsin complex measurement http://www.ebi.ac.uk/efo/EFO_0008018 GCST90237573 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. P-selectin level in Chronic kidney disease with hypertension and no diabetes (4154_57) 466 African American individuals NA Illumina [14870897] (imputed) 1 P-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008254 GCST90237574 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin level in Chronic kidney disease with hypertension and no diabetes (4155_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90237575 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming growth factor beta-2 level in Chronic kidney disease with hypertension and no diabetes (4156_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 transforming growth factor beta-2 measurement http://www.ebi.ac.uk/efo/EFO_0020781 GCST90237576 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Maleylacetoacetate isomerase level in Chronic kidney disease with hypertension and no diabetes (16872_248) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of maleylacetoacetate isomerase in blood serum http://purl.obolibrary.org/obo/OBA_2041811 GCST90234599 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein mago nashi homolog 2 level in Chronic kidney disease with hypertension and no diabetes (16875_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein mago nashi homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042273 GCST90234600 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionine-R-sulfoxide reductase B2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (16877_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methionine-R-sulfoxide reductase B2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042443 GCST90234601 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14 kDa phosphohistidine phosphatase level in Chronic kidney disease with hypertension and no diabetes (16882_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 14 kDa phosphohistidine phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2042879 GCST90234602 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-4A level in Chronic kidney disease with hypertension and no diabetes (16883_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-4A in blood serum http://purl.obolibrary.org/obo/OBA_2043164 GCST90234603 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated protein RP/EB family member 3 level in Chronic kidney disease with hypertension and no diabetes (16885_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated protein RP/EB family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042298 GCST90234604 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-tRNA hydrolase 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (16887_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-tRNA hydrolase 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043112 GCST90234605 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADAMTS-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (16890_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADAMTS-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040506 GCST90234606 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleotide pyrophosphatase/phosphodiesterase family member 2 level in Chronic kidney disease with hypertension and no diabetes (16892_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ectonucleotide pyrophosphatase/phosphodiesterase family member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041480 GCST90234607 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxysterol-binding protein-related protein 9 level in Chronic kidney disease with hypertension and no diabetes (16899_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxysterol-binding protein-related protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2042714 GCST90234608 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAM domain-containing glycosylphosphatidylinositol anchor protein 1 level in Chronic kidney disease with hypertension and no diabetes (16900_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MAM domain-containing glycosylphosphatidylinositol anchor protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042317 GCST90234609 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysosome-associated membrane glycoprotein 1 level in Chronic kidney disease with hypertension and no diabetes (16902_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysosome-associated membrane glycoprotein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040382 GCST90234610 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell adhesion molecule 2 level in Chronic kidney disease with hypertension and no diabetes (16907_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell adhesion molecule 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040872 GCST90234611 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oligodendrocyte-myelin glycoprotein level in Chronic kidney disease with hypertension and no diabetes (16908_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oligodendrocyte-myelin glycoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2042706 GCST90234612 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Monocyte differentiation antigen CD14, soluble level in Chronic kidney disease with hypertension and no diabetes (16914_104) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of CD14 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040350 GCST90234613 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-4A level in Chronic kidney disease with hypertension and no diabetes (16915_153) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-4A in blood serum http://purl.obolibrary.org/obo/OBA_2043430 GCST90234614 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT and NTRK-like protein 6 level in Chronic kidney disease with hypertension and no diabetes (16916_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLIT and NTRK-like protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043550 GCST90234615 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 3 level in Chronic kidney disease with hypertension and no diabetes (16918_198) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Toll-like receptor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040250 GCST90234616 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-CoA-binding protein level in Chronic kidney disease with hypertension and no diabetes (16919_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-CoA-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2041235 GCST90234617 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin-B3 level in Chronic kidney disease with hypertension and no diabetes (16922_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plexin-B3 in blood serum http://purl.obolibrary.org/obo/OBA_2042939 GCST90234618 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Profilin-2 level in Chronic kidney disease with hypertension and no diabetes (16923_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of profilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042856 GCST90234619 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alkaline phosphatase, tissue-nonspecific isozyme level in Chronic kidney disease with hypertension and no diabetes (16926_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alkaline phosphatase, tissue-nonspecific isozyme in blood serum http://purl.obolibrary.org/obo/OBA_2040575 GCST90234620 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation factor XIII level in Chronic kidney disease with hypertension and no diabetes (16927_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 coagulation factor measurement http://www.ebi.ac.uk/efo/EFO_0004634 GCST90234621 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Estrogen sulfotransferase level in Chronic kidney disease with hypertension and no diabetes (16932_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 1E1 in blood serum http://purl.obolibrary.org/obo/OBA_2044790 GCST90234622 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemoglobin subunit beta level in Chronic kidney disease with hypertension and no diabetes (17137_160) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of hemoglobin subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2044809 GCST90234623 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase A1 level in Chronic kidney disease with hypertension and no diabetes (17138_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041802 GCST90234624 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A8/A9 heterodimer level in Chronic kidney disease with hypertension and no diabetes (17145_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein s100-a9 measurement http://www.ebi.ac.uk/efo/EFO_0020687 GCST90234625 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Flavin reductase (NADPH) level in Chronic kidney disease with hypertension and no diabetes (17148_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of flavin reductase in blood serum http://purl.obolibrary.org/obo/OBA_2040809 GCST90234626 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 10 kDa heat shock protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17150_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 10 kDa heat shock protein, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041953 GCST90234627 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 3 level in Chronic kidney disease with hypertension and no diabetes (17151_84) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interferon regulatory factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040375 GCST90234628 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DS4 level in Chronic kidney disease with hypertension and no diabetes (17152_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of killer cell immunoglobulin-like receptor 2DS4 in blood serum http://purl.obolibrary.org/obo/OBA_2042108 GCST90234629 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DL3 level in Chronic kidney disease with hypertension and no diabetes (17153_46) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of killer cell immunoglobulin-like receptor 2DL3 in blood serum http://purl.obolibrary.org/obo/OBA_2042105 GCST90234630 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin E synthase 3 level in Chronic kidney disease with hypertension and no diabetes (17154_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prostaglandin E synthase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043091 GCST90234631 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase DCLK1 level in Chronic kidney disease with hypertension and no diabetes (17156_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase DCLK1 in blood serum http://purl.obolibrary.org/obo/OBA_2041240 GCST90234632 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 G1 level in Chronic kidney disease with hypertension and no diabetes (17158_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ubiquitin-conjugating enzyme E2 G1 in blood serum http://purl.obolibrary.org/obo/OBA_2043995 GCST90234633 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (17161_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dolichyl-diphosphooligosaccharide--protein glycosyltransferase 48 kDa subunit in blood serum http://purl.obolibrary.org/obo/OBA_2041256 GCST90234634 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A3 level in Chronic kidney disease with hypertension and no diabetes (17163_117) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A3 in blood serum http://purl.obolibrary.org/obo/OBA_2040600 GCST90234635 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A4 level in Chronic kidney disease with hypertension and no diabetes (17164_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of annexin A4 in blood serum http://purl.obolibrary.org/obo/OBA_2040601 GCST90234636 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-thromboglobulin level in Chronic kidney disease with hypertension and no diabetes (17165_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of platelet basic protein in blood serum http://purl.obolibrary.org/obo/OBA_2042981 GCST90234637 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 8 isoform F level in Chronic kidney disease with hypertension and no diabetes (17166_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of fibroblast growth factor 8 in blood serum http://purl.obolibrary.org/obo/OBA_2041575 GCST90234638 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcitonin gene-related peptide 2 level in Chronic kidney disease with hypertension and no diabetes (17170_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcitonin gene-related peptide 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040876 GCST90234639 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Statherin level in Chronic kidney disease with hypertension and no diabetes (17172_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of statherin in blood serum http://purl.obolibrary.org/obo/OBA_2043695 GCST90234640 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity mitogen-activated protein kinase kinase 6 level in Chronic kidney disease with hypertension and no diabetes (17175_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity mitogen-activated protein kinase kinase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040428 GCST90234641 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PC4 and SFRS1-interacting protein level in Chronic kidney disease with hypertension and no diabetes (17176_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PC4 and SFRS1-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2040443 GCST90234642 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BAG family molecular chaperone regulator 1 level in Chronic kidney disease with hypertension and no diabetes (17195_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BAG family molecular chaperone regulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040765 GCST90234643 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent Clp protease proteolytic subunit, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17196_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent Clp protease proteolytic subunit, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044271 GCST90234644 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hypoxia-inducible factor 1-alpha inhibitor level in Chronic kidney disease with hypertension and no diabetes (17199_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hypoxia-inducible factor 1-alpha inhibitor in blood serum http://purl.obolibrary.org/obo/OBA_2041875 GCST90234645 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DL1 level in Chronic kidney disease with hypertension and no diabetes (17200_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of killer cell immunoglobulin-like receptor 2DL1 in blood serum http://purl.obolibrary.org/obo/OBA_2042103 GCST90234646 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death protein 4 level in Chronic kidney disease with hypertension and no diabetes (17202_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of programmed cell death protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042812 GCST90234647 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phenylethanolamine N-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (17204_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phenylethanolamine N-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042952 GCST90234648 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V(D)J recombination-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (11311_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V(D)J recombination-activating protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040446 GCST90233186 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mismatch repair endonuclease PMS2 level in Chronic kidney disease with hypertension and no diabetes (11312_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mismatch repair endonuclease PMS2 in blood serum http://purl.obolibrary.org/obo/OBA_2042945 GCST90233187 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pterin-4-alpha-carbinolamine dehydratase level in Chronic kidney disease with hypertension and no diabetes (11313_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pterin-4-alpha-carbinolamine dehydratase in blood serum http://purl.obolibrary.org/obo/OBA_2042777 GCST90233188 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1D level in Chronic kidney disease with hypertension and no diabetes (11315_148) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1D in blood serum http://purl.obolibrary.org/obo/OBA_2042993 GCST90233189 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein A-V level in Chronic kidney disease with hypertension and no diabetes (11318_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apolipoprotein A-V in blood serum http://purl.obolibrary.org/obo/OBA_2040623 GCST90233190 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Double-strand break repair protein MRE11 level in Chronic kidney disease with hypertension and no diabetes (11319_106) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of double-strand break repair protein MRE11 in blood serum http://purl.obolibrary.org/obo/OBA_2042415 GCST90233191 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase CHFR level in Chronic kidney disease with hypertension and no diabetes (11320_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase CHFR in blood serum http://purl.obolibrary.org/obo/OBA_2041003 GCST90233192 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxidasin-like protein level in Chronic kidney disease with hypertension and no diabetes (11324_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable oxidoreductase PXDNL in blood serum http://purl.obolibrary.org/obo/OBA_2043121 GCST90233193 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BTG2 level in Chronic kidney disease with hypertension and no diabetes (11325_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BTG2 in blood serum http://purl.obolibrary.org/obo/OBA_2040833 GCST90233194 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein kinase CLK2 level in Chronic kidney disease with hypertension and no diabetes (11327_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein kinase CLK2 in blood serum http://purl.obolibrary.org/obo/OBA_2041053 GCST90233195 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U6 snRNA phosphodiesterase level in Chronic kidney disease with hypertension and no diabetes (11328_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U6 snRNA phosphodiesterase in blood serum http://purl.obolibrary.org/obo/OBA_2044862 GCST90233196 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase II subunit beta level in Chronic kidney disease with hypertension and no diabetes (11330_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of casein kinase II subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2041173 GCST90233197 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 25 level in Chronic kidney disease with hypertension and no diabetes (11333_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 25 in blood serum http://purl.obolibrary.org/obo/OBA_2040651 GCST90233198 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily B member 3 level in Chronic kidney disease with hypertension and no diabetes (11334_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily B member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042199 GCST90233199 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fanconi anemia group F protein level in Chronic kidney disease with hypertension and no diabetes (11336_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fanconi anemia group F protein in blood serum http://purl.obolibrary.org/obo/OBA_2041547 GCST90233200 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase BLK level in Chronic kidney disease with hypertension and no diabetes (11338_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein kinase BLK in blood serum http://purl.obolibrary.org/obo/OBA_2040802 GCST90233201 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (11342_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233202 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transaldolase level in Chronic kidney disease with hypertension and no diabetes (11347_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transaldolase in blood serum http://purl.obolibrary.org/obo/OBA_2043774 GCST90233203 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolyl 4-hydroxylase subunit alpha-2 level in Chronic kidney disease with hypertension and no diabetes (11348_132) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prolyl 4-hydroxylase subunit alpha-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042732 GCST90233204 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase CHIP level in Chronic kidney disease with hypertension and no diabetes (11350_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 E3 ubiquitin-protein ligase CHIP measurement http://www.ebi.ac.uk/efo/EFO_0021904 GCST90233205 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Non-homologous end-joining factor 1 level in Chronic kidney disease with hypertension and no diabetes (11351_233) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of non-homologous end-joining factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042578 GCST90233206 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Titin level in Chronic kidney disease with hypertension and no diabetes (11352_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of titin in blood serum http://purl.obolibrary.org/obo/OBA_2043958 GCST90233207 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mothers against decapentaplegic homolog 2 level in Chronic kidney disease with hypertension and no diabetes (11353_143) 466 African American individuals NA Illumina [14870897] (imputed) 0 mothers against decapentaplegic homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0021914 GCST90233208 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1 level in Chronic kidney disease with hypertension and no diabetes (11354_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042918 GCST90233209 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 5A-2 level in Chronic kidney disease with hypertension and no diabetes (11355_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 5A-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041458 GCST90233210 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein DGCR14 level in Chronic kidney disease with hypertension and no diabetes (11356_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of splicing factor ESS-2 homolog in blood serum http://purl.obolibrary.org/obo/OBA_2041290 GCST90233211 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth factor receptor-bound protein 10 level in Chronic kidney disease with hypertension and no diabetes (11358_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth factor receptor-bound protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041783 GCST90233212 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonucleoside-diphosphate reductase large subunit level in Chronic kidney disease with hypertension and no diabetes (11360_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonucleoside-diphosphate reductase large subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043346 GCST90233213 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thymidine phosphorylase level in Chronic kidney disease with hypertension and no diabetes (11361_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thymidine phosphorylase in blood serum http://purl.obolibrary.org/obo/OBA_2043975 GCST90233214 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aquaporin-4 level in Chronic kidney disease with hypertension and no diabetes (11363_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aquaporin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040635 GCST90233215 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitofusin-1 level in Chronic kidney disease with hypertension and no diabetes (11364_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitofusin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042353 GCST90233216 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Teneurin-4 level in Chronic kidney disease with hypertension and no diabetes (11365_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of teneurin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042694 GCST90233217 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase class-3 level in Chronic kidney disease with hypertension and no diabetes (11369_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alcohol dehydrogenase class-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040517 GCST90233218 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable G-protein coupled receptor 101 level in Chronic kidney disease with hypertension and no diabetes (11371_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable G-protein coupled receptor 101 in blood serum http://purl.obolibrary.org/obo/OBA_2040306 GCST90233219 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 18 level in Chronic kidney disease with hypertension and no diabetes (11372_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 18 in blood serum http://purl.obolibrary.org/obo/OBA_2044192 GCST90233220 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein L2 level in Chronic kidney disease with hypertension and no diabetes (11375_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein L2 in blood serum http://purl.obolibrary.org/obo/OBA_2041608 GCST90233221 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase class 4 mu/sigma chain level in Chronic kidney disease with hypertension and no diabetes (11377_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of all-trans-retinol dehydrogenase [NAD(+)] ADH7 in blood serum http://purl.obolibrary.org/obo/OBA_2040519 GCST90233222 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase SYK level in Chronic kidney disease with hypertension and no diabetes (11378_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233223 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein 24 level in Chronic kidney disease with hypertension and no diabetes (11380_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2043206 GCST90233224 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribose-phosphate pyrophosphokinase 1 level in Chronic kidney disease with hypertension and no diabetes (11381_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribose-phosphate pyrophosphokinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043039 GCST90233225 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biliverdin reductase A level in Chronic kidney disease with hypertension and no diabetes (11382_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of biliverdin reductase A in blood serum http://purl.obolibrary.org/obo/OBA_2040808 GCST90233226 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type II cytoskeletal 7 level in Chronic kidney disease with hypertension and no diabetes (11383_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type II cytoskeletal 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042146 GCST90233227 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-dependent transcription factor ATF-6 beta level in Chronic kidney disease with hypertension and no diabetes (11387_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-dependent transcription factor ATF-6 beta in blood serum http://purl.obolibrary.org/obo/OBA_2040716 GCST90233228 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 2 level in Chronic kidney disease with hypertension and no diabetes (11388_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WAP four-disulfide core domain protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044636 GCST90233229 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase-related protein level in Chronic kidney disease with hypertension and no diabetes (11390_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbonic anhydrase-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2040861 GCST90233230 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-tyrosine kinase 2-beta level in Chronic kidney disease with hypertension and no diabetes (11395_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233231 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynein intermediate chain 1, axonemal level in Chronic kidney disease with hypertension and no diabetes (11396_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynein axonemal intermediate chain 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041325 GCST90233232 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF146 level in Chronic kidney disease with hypertension and no diabetes (11401_181) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RNF146 in blood serum http://purl.obolibrary.org/obo/OBA_2043292 GCST90233233 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase 2C level in Chronic kidney disease with hypertension and no diabetes (11402_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone-lysine N-methyltransferase 2C in blood serum http://purl.obolibrary.org/obo/OBA_2042379 GCST90233234 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase recruitment domain-containing protein 9 level in Chronic kidney disease with hypertension and no diabetes (11405_150) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caspase recruitment domain-containing protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2040899 GCST90233235 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cGMP-specific 3',5'-cyclic phosphodiesterase level in Chronic kidney disease with hypertension and no diabetes (16805_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 cGMP-specific 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0008081 GCST90234574 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Troponin T, fast skeletal muscle level in Chronic kidney disease with hypertension and no diabetes (16807_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 troponin i, fast skeletal muscle measurement http://www.ebi.ac.uk/efo/EFO_0020789 GCST90234575 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleoside diphosphate kinase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (16809_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleoside diphosphate kinase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042595 GCST90234576 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab GDP dissociation inhibitor alpha level in Chronic kidney disease with hypertension and no diabetes (16810_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 rab gdp dissociation inhibitor beta measurement http://www.ebi.ac.uk/efo/EFO_0020697 GCST90234577 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Four and a half LIM domains protein 1 level in Chronic kidney disease with hypertension and no diabetes (16814_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of four and a half LIM domains protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041581 GCST90234578 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUB domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (16818_200) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CUB domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040956 GCST90234579 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein L3 level in Chronic kidney disease with hypertension and no diabetes (16823_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apolipoprotein L3 in blood serum http://purl.obolibrary.org/obo/OBA_2040631 GCST90234580 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ataxin-3 level in Chronic kidney disease with hypertension and no diabetes (16825_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ataxin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040738 GCST90234581 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(VI) chain level in Chronic kidney disease with hypertension and no diabetes (16828_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of collagen alpha-1(VI) chain in blood serum http://purl.obolibrary.org/obo/OBA_2040438 GCST90234582 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Docking protein 1 level in Chronic kidney disease with hypertension and no diabetes (16831_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of docking protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041343 GCST90234583 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement factor H-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (16836_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement factor H-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0600056 GCST90234584 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myelin protein zero-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (16845_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myelin protein zero-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042410 GCST90234585 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-3B level in Chronic kidney disease with hypertension and no diabetes (16847_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-3B in blood serum http://purl.obolibrary.org/obo/OBA_2043159 GCST90234586 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 5 level in Chronic kidney disease with hypertension and no diabetes (16850_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043262 GCST90234587 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein SCO2 homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (16851_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein SCO2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043408 GCST90234588 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Na(+)/H(+) exchange regulatory cofactor NHE-RF3 level in Chronic kidney disease with hypertension and no diabetes (16852_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Na(+)/H(+) exchange regulatory cofactor NHE-RF3 in blood serum http://purl.obolibrary.org/obo/OBA_2042839 GCST90234589 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nicotinamide riboside kinase 1 level in Chronic kidney disease with hypertension and no diabetes (16853_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 nicotinamide riboside measurement http://www.ebi.ac.uk/efo/EFO_0800156 GCST90234590 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U6 snRNA-associated Sm-like protein LSm4 level in Chronic kidney disease with hypertension and no diabetes (16854_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U6 snRNA-associated Sm-like protein LSm4 in blood serum http://purl.obolibrary.org/obo/OBA_2042243 GCST90234591 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated protein RP/EB family member 2 level in Chronic kidney disease with hypertension and no diabetes (16856_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated protein RP/EB family member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042297 GCST90234592 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-2A level in Chronic kidney disease with hypertension and no diabetes (16857_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-2A in blood serum http://purl.obolibrary.org/obo/OBA_2043151 GCST90234593 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Reticulocalbin-3 level in Chronic kidney disease with hypertension and no diabetes (16858_384) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of reticulocalbin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043220 GCST90234594 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endophilin-B1 level in Chronic kidney disease with hypertension and no diabetes (16859_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endophilin-B1 in blood serum http://purl.obolibrary.org/obo/OBA_2043493 GCST90234595 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acylneuraminate-9-phosphatase level in Chronic kidney disease with hypertension and no diabetes (16863_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acylneuraminate-9-phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2042504 GCST90234596 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TATA-binding protein-associated factor 2N level in Chronic kidney disease with hypertension and no diabetes (16865_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TATA-binding protein-associated factor 2N in blood serum http://purl.obolibrary.org/obo/OBA_2043771 GCST90234597 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 16 level in Chronic kidney disease with hypertension and no diabetes (16867_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 16 in blood serum http://purl.obolibrary.org/obo/OBA_2042808 GCST90234598 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11270_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044545 GCST90233161 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase theta-2B level in Chronic kidney disease with hypertension and no diabetes (11273_176) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase theta-2B in blood serum http://purl.obolibrary.org/obo/OBA_2044307 GCST90233162 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 1B level in Chronic kidney disease with hypertension and no diabetes (11275_94) 466 African American individuals NA Illumina [14870897] (imputed) 1 low-density lipoprotein receptor-related protein 1B measurement http://www.ebi.ac.uk/efo/EFO_0021873 GCST90233163 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-dependent transcription factor ATF-6 alpha level in Chronic kidney disease with hypertension and no diabetes (11277_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-dependent transcription factor ATF-6 alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040715 GCST90233164 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-2(XI) chain level in Chronic kidney disease with hypertension and no diabetes (11278_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-2(XI) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041081 GCST90233165 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate decarboxylase 1 level in Chronic kidney disease with hypertension and no diabetes (11280_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamate decarboxylase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041651 GCST90233166 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth factor receptor-bound protein 7 level in Chronic kidney disease with hypertension and no diabetes (11281_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth factor receptor-bound protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041785 GCST90233167 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage scavenger receptor types I and II level in Chronic kidney disease with hypertension and no diabetes (11282_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage scavenger receptor types I and II measurement http://www.ebi.ac.uk/efo/EFO_0008222 GCST90233168 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DDB1- and CUL4-associated factor 5 level in Chronic kidney disease with hypertension and no diabetes (11283_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DDB1- and CUL4-associated factor 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044579 GCST90233169 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte-associated immunoglobulin-like receptor 1 level in Chronic kidney disease with hypertension and no diabetes (11284_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte-associated immunoglobulin-like receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040345 GCST90233170 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hematopoietic progenitor cell antigen CD34 level in Chronic kidney disease with hypertension and no diabetes (11285_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD34 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040225 GCST90233171 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Selenoprotein S level in Chronic kidney disease with hypertension and no diabetes (11286_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of selenoprotein S in blood serum http://purl.obolibrary.org/obo/OBA_2043426 GCST90233172 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome b5 level in Chronic kidney disease with hypertension and no diabetes (11287_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome b5 in blood serum http://purl.obolibrary.org/obo/OBA_2041209 GCST90233173 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic purine 5'-nucleotidase level in Chronic kidney disease with hypertension and no diabetes (11288_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosolic purine 5'-nucleotidase in blood serum http://purl.obolibrary.org/obo/OBA_2042649 GCST90233174 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase I isoform delta level in Chronic kidney disease with hypertension and no diabetes (11289_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of casein kinase I isoform delta in blood serum http://purl.obolibrary.org/obo/OBA_2041170 GCST90233175 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor class A member 3 level in Chronic kidney disease with hypertension and no diabetes (11292_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90233176 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat neuronal protein 1 level in Chronic kidney disease with hypertension and no diabetes (11293_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233177 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane and coiled-coil domains protein 3 level in Chronic kidney disease with hypertension and no diabetes (11294_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233178 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurogenic locus notch homolog protein 2 level in Chronic kidney disease with hypertension and no diabetes (11297_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90233179 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sortilin level in Chronic kidney disease with hypertension and no diabetes (11300_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 sortilin measurement http://www.ebi.ac.uk/efo/EFO_0600000 GCST90233180 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin-R level in Chronic kidney disease with hypertension and no diabetes (11302_237) 466 African American individuals NA Illumina [14870897] (imputed) 0 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90233181 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deoxynucleoside triphosphate triphosphohydrolase SAMHD1 level in Chronic kidney disease with hypertension and no diabetes (11303_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deoxynucleoside triphosphate triphosphohydrolase SAMHD1 in blood serum http://purl.obolibrary.org/obo/OBA_2043375 GCST90233182 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD4-like E3 ubiquitin-protein ligase WWP1 level in Chronic kidney disease with hypertension and no diabetes (11307_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD4-like E3 ubiquitin-protein ligase WWP1 in blood serum http://purl.obolibrary.org/obo/OBA_2040421 GCST90233183 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-responsive element-binding protein 3-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (11308_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cyclic AMP-responsive element-binding protein 3-like protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041134 GCST90233184 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmoglein-3 level in Chronic kidney disease with hypertension and no diabetes (11310_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of desmoglein-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041369 GCST90233185 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 4 catalytic subunit level in Chronic kidney disease with hypertension and no diabetes (22534_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine/threonine-protein phosphatase 4 catalytic subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043013 GCST90236112 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1 regulatory subunit 42 level in Chronic kidney disease with hypertension and no diabetes (22536_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1 regulatory subunit 42 in blood serum http://purl.obolibrary.org/obo/OBA_2044729 GCST90236113 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type 7 level in Chronic kidney disease with hypertension and no diabetes (22540_129) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit beta type-7 in blood serum http://purl.obolibrary.org/obo/OBA_2043072 GCST90236114 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA replication complex GINS protein PSF1 level in Chronic kidney disease with hypertension and no diabetes (22541_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA replication complex GINS protein PSF1 in blood serum http://purl.obolibrary.org/obo/OBA_2041719 GCST90236115 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA repair protein RAD51 homolog 3 level in Chronic kidney disease with hypertension and no diabetes (22544_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA repair protein RAD51 homolog 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043182 GCST90236116 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding Raly-like protein level in Chronic kidney disease with hypertension and no diabetes (22545_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding Raly-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2043187 GCST90236117 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding motif, single-stranded-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (22547_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding motif, single-stranded-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043210 GCST90236118 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 13 level in Chronic kidney disease with hypertension and no diabetes (22548_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of regulator of G-protein signaling 13 in blood serum http://purl.obolibrary.org/obo/OBA_2043254 GCST90236119 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S ribosomal protein L38 level in Chronic kidney disease with hypertension and no diabetes (22553_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S ribosomal protein L38 in blood serum http://purl.obolibrary.org/obo/OBA_2043322 GCST90236120 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L10, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22554_101) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L10, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042422 GCST90236121 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein UNQ511/PRO1026 level in Chronic kidney disease with hypertension and no diabetes (22561_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ly6/PLAUR domain-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044571 GCST90236122 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kin of IRRE-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (22563_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kin of IRRE-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042110 GCST90236123 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor class A domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (22564_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor class A domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044754 GCST90236124 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pituitary adenylate cyclase-activating polypeptide type I receptor level in Chronic kidney disease with hypertension and no diabetes (22566_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pituitary adenylate cyclase-activating polypeptide type I receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040511 GCST90236125 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmoglein-4 level in Chronic kidney disease with hypertension and no diabetes (22568_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of desmoglein-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041370 GCST90236126 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TGF-beta receptor type-1 level in Chronic kidney disease with hypertension and no diabetes (22569_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TGF-beta receptor type-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040188 GCST90236127 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pepsin A-4 level in Chronic kidney disease with hypertension and no diabetes (22572_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pepsin A-4 in blood serum http://purl.obolibrary.org/obo/OBA_2044775 GCST90236128 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD209 antigen level in Chronic kidney disease with hypertension and no diabetes (22576_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 CD209 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008077 GCST90236129 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 14 level in Chronic kidney disease with hypertension and no diabetes (22577_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90236130 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Roundabout homolog 2 level in Chronic kidney disease with hypertension and no diabetes (22578_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 roundabout homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0020713 GCST90236131 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexin-1-beta level in Chronic kidney disease with hypertension and no diabetes (22579_93) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurexin-1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020596 GCST90236132 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A2 level in Chronic kidney disease with hypertension and no diabetes (22580_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A2 measurement http://www.ebi.ac.uk/efo/EFO_0021944 GCST90236133 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2D ligand 2 level in Chronic kidney disease with hypertension and no diabetes (22583_47) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of UL16-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044029 GCST90236134 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 6 level in Chronic kidney disease with hypertension and no diabetes (22584_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor-related protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042235 GCST90236135 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-4 level in Chronic kidney disease with hypertension and no diabetes (22585_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frizzled-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040301 GCST90236136 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-5A level in Chronic kidney disease with hypertension and no diabetes (17205_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-5A in blood serum http://purl.obolibrary.org/obo/OBA_2043166 GCST90234649 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfotransferase family cytosolic 2B member 1 level in Chronic kidney disease with hypertension and no diabetes (17209_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 2B1 in blood serum http://purl.obolibrary.org/obo/OBA_2043729 GCST90234650 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell leukemia/lymphoma protein 1A level in Chronic kidney disease with hypertension and no diabetes (17210_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-cell leukemia/lymphoma protein 1A in blood serum http://purl.obolibrary.org/obo/OBA_2043813 GCST90234651 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mimecan level in Chronic kidney disease with hypertension and no diabetes (17224_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mimecan in blood serum http://purl.obolibrary.org/obo/OBA_2042696 GCST90234652 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plastin-2 level in Chronic kidney disease with hypertension and no diabetes (17231_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plastin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042176 GCST90234653 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Selenoprotein H level in Chronic kidney disease with hypertension and no diabetes (17319_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of selenoprotein H in blood serum http://purl.obolibrary.org/obo/OBA_2043424 GCST90234654 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase level in Chronic kidney disease with hypertension and no diabetes (17320_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of L-aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase in blood serum http://purl.obolibrary.org/obo/OBA_2040456 GCST90234655 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylate kinase level in Chronic kidney disease with hypertension and no diabetes (17325_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanylate kinase in blood serum http://purl.obolibrary.org/obo/OBA_2041823 GCST90234656 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 23 level in Chronic kidney disease with hypertension and no diabetes (17326_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 23 in blood serum http://purl.obolibrary.org/obo/OBA_2041385 GCST90234657 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein canopy homolog 3 level in Chronic kidney disease with hypertension and no diabetes (17327_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein canopy homolog 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041070 GCST90234658 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-hydroxybutyrate dehydrogenase type 2 level in Chronic kidney disease with hypertension and no diabetes (17329_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dehydrogenase/reductase SDR family member 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040790 GCST90234659 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kremen protein 1 level in Chronic kidney disease with hypertension and no diabetes (17331_138) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Kremen protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042136 GCST90234660 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroguidin level in Chronic kidney disease with hypertension and no diabetes (22512_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroguidin in blood serum http://purl.obolibrary.org/obo/OBA_2042576 GCST90236099 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein naked cuticle homolog 2 level in Chronic kidney disease with hypertension and no diabetes (22514_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein naked cuticle homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042585 GCST90236100 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 SUMO-protein ligase NSE2 level in Chronic kidney disease with hypertension and no diabetes (22517_106) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 SUMO-protein ligase NSE2 in blood serum http://purl.obolibrary.org/obo/OBA_2042647 GCST90236101 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein OTX2 level in Chronic kidney disease with hypertension and no diabetes (22521_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein OTX2 in blood serum http://purl.obolibrary.org/obo/OBA_2042724 GCST90236102 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyadenylate-binding protein 5 level in Chronic kidney disease with hypertension and no diabetes (22523_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyadenylate-binding protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042736 GCST90236103 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paired box protein Pax-3 level in Chronic kidney disease with hypertension and no diabetes (22525_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of paired box protein Pax-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042769 GCST90236104 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyruvate dehydrogenase E1 component beta subunit level in Chronic kidney disease with hypertension and no diabetes (22526_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyruvate dehydrogenase E1 component subunit beta, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042826 GCST90236105 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ and LIM domain protein 3 level in Chronic kidney disease with hypertension and no diabetes (22527_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ and LIM domain protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042834 GCST90236106 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PHD finger protein 11 level in Chronic kidney disease with hypertension and no diabetes (22528_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PHD finger protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042872 GCST90236107 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PHD finger protein 6 level in Chronic kidney disease with hypertension and no diabetes (22529_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PHD finger protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042874 GCST90236108 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phytanoyl-CoA dioxygenase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (22530_111) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phytanoyl-CoA dioxygenase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042881 GCST90236109 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pituitary homeobox 2 level in Chronic kidney disease with hypertension and no diabetes (22531_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pituitary homeobox 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040196 GCST90236110 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 1 regulatory subunit 10 level in Chronic kidney disease with hypertension and no diabetes (22533_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein phosphatase 1 regulatory subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043000 GCST90236111 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isobutyryl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11406_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isobutyryl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040467 GCST90233236 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipid scramblase 3 level in Chronic kidney disease with hypertension and no diabetes (11407_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipid scramblase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042933 GCST90233237 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. F-box/LRR-repeat protein 4 level in Chronic kidney disease with hypertension and no diabetes (11416_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233238 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EH domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (11421_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EH domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041435 GCST90233239 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein DLX-3 level in Chronic kidney disease with hypertension and no diabetes (11422_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein DLX-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041318 GCST90233240 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fumarylacetoacetase level in Chronic kidney disease with hypertension and no diabetes (11424_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fumarylacetoacetase in blood serum http://purl.obolibrary.org/obo/OBA_2041542 GCST90233241 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ and LIM domain protein 1 level in Chronic kidney disease with hypertension and no diabetes (11428_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ and LIM domain protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042833 GCST90233242 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoproteins C1/C2 level in Chronic kidney disease with hypertension and no diabetes (11429_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoproteins C1/C2 in blood serum http://purl.obolibrary.org/obo/OBA_2041904 GCST90233243 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase DTX1 level in Chronic kidney disease with hypertension and no diabetes (11430_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase DTX1 in blood serum http://purl.obolibrary.org/obo/OBA_2041375 GCST90233244 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent DNA helicase Q1 level in Chronic kidney disease with hypertension and no diabetes (11431_235) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent DNA helicase Q1 in blood serum http://purl.obolibrary.org/obo/OBA_2043228 GCST90233245 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyglutamine-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (11432_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyglutamine-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043015 GCST90233246 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tectonic-2 level in Chronic kidney disease with hypertension and no diabetes (11433_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tectonic-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043819 GCST90233247 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-internexin level in Chronic kidney disease with hypertension and no diabetes (11436_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-internexin in blood serum http://purl.obolibrary.org/obo/OBA_2042025 GCST90233248 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 2 level in Chronic kidney disease with hypertension and no diabetes (11438_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044285 GCST90233249 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rhophilin-2 level in Chronic kidney disease with hypertension and no diabetes (11439_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of rhophilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043270 GCST90233250 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junction plakoglobin level in Chronic kidney disease with hypertension and no diabetes (16768_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of junction plakoglobin in blood serum http://purl.obolibrary.org/obo/OBA_2042079 GCST90234564 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related C3 botulinum toxin substrate 3 level in Chronic kidney disease with hypertension and no diabetes (16769_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 ras-related C3 botulinum toxin substrate 3 measurement http://www.ebi.ac.uk/efo/EFO_0021987 GCST90234565 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lithostathine-1-beta level in Chronic kidney disease with hypertension and no diabetes (16770_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lithostathine-1-beta in blood serum http://purl.obolibrary.org/obo/OBA_2043231 GCST90234566 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal peptide, CUB and EGF-like domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (16773_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal peptide, CUB and EGF-like domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044438 GCST90234567 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (16780_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90234568 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic endo-beta-N-acetylglucosaminidase level in Chronic kidney disease with hypertension and no diabetes (16781_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosolic endo-beta-N-acetylglucosaminidase in blood serum http://purl.obolibrary.org/obo/OBA_2041477 GCST90234569 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Defensin-5 level in Chronic kidney disease with hypertension and no diabetes (16785_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of defensin alpha 5 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044902 GCST90234570 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 5 level in Chronic kidney disease with hypertension and no diabetes (16792_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sialic acid-binding Ig-like lectin 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040358 GCST90234571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. OCIA domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (16802_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 OCIA domain-containing protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008252 GCST90234572 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calretinin level in Chronic kidney disease with hypertension and no diabetes (16803_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calretinin in blood serum http://purl.obolibrary.org/obo/OBA_2040875 GCST90234573 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NSFL1 cofactor p47 level in Chronic kidney disease with hypertension and no diabetes (4250_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 NFSL1 cofactor p47 measurement http://www.ebi.ac.uk/efo/EFO_0020612 GCST90237602 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NudC domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (4254_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 NudC domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020616 GCST90237603 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proliferation-associated protein 2G4 level in Chronic kidney disease with hypertension and no diabetes (4258_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 proliferation-associated protein 2g4 measurement http://www.ebi.ac.uk/efo/EFO_0020658 GCST90237604 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum paraoxonase/arylesterase 1 level in Chronic kidney disease with hypertension and no diabetes (4261_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 serum paraoxonase/arylesterase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020736 GCST90237605 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pescadillo homolog level in Chronic kidney disease with hypertension and no diabetes (4267_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 pescadillo homolog measurement http://www.ebi.ac.uk/efo/EFO_0020633 GCST90237606 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prefoldin subunit 5 level in Chronic kidney disease with hypertension and no diabetes (4271_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 prefoldin subunit 5 measurement http://www.ebi.ac.uk/efo/EFO_0020652 GCST90237607 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucose-6-phosphate isomerase level in Chronic kidney disease with hypertension and no diabetes (4272_46) 466 African American individuals NA Illumina [14870897] (imputed) 1 glucose-6-phosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020407 GCST90237608 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylethanolamine-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (4276_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 phosphatidylethanolamine-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020634 GCST90237609 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase level in Chronic kidney disease with hypertension and no diabetes (4278_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein disulfide-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020669 GCST90237610 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-2 level in Chronic kidney disease with hypertension and no diabetes (4280_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 proteasome subunit alpha type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020664 GCST90237611 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding nuclear protein Ran level in Chronic kidney disease with hypertension and no diabetes (4282_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 GTP-binding nuclear protein ran measurement http://www.ebi.ac.uk/efo/EFO_0020431 GCST90237612 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein 39 level in Chronic kidney disease with hypertension and no diabetes (4284_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 rna-binding protein 39 measurement http://www.ebi.ac.uk/efo/EFO_0020712 GCST90237613 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-soluble NSF attachment protein level in Chronic kidney disease with hypertension and no diabetes (4292_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-soluble NSF attachment protein measurement http://www.ebi.ac.uk/efo/EFO_0020140 GCST90237614 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sphingosine kinase 1 level in Chronic kidney disease with hypertension and no diabetes (4294_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 sphingosine kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020750 GCST90237615 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spondin-1 level in Chronic kidney disease with hypertension and no diabetes (4297_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90237616 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thymidine kinase, cytosolic level in Chronic kidney disease with hypertension and no diabetes (4301_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 thymidine kinase, cytosolic measurement http://www.ebi.ac.uk/efo/EFO_0020773 GCST90237617 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ligand-dependent nuclear receptor corepressor-like protein level in Chronic kidney disease with hypertension and no diabetes (4304_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 ligand-dependent nuclear receptor corepressor-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020536 GCST90237618 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transketolase level in Chronic kidney disease with hypertension and no diabetes (4306_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 transketolase measurement http://www.ebi.ac.uk/efo/EFO_0020783 GCST90237619 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Triosephosphate isomerase level in Chronic kidney disease with hypertension and no diabetes (4309_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 triosephosphate isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020785 GCST90237620 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. dCTP pyrophosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (4314_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 DCTP pyrophosphatase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020314 GCST90237621 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 6 level in Chronic kidney disease with hypertension and no diabetes (4318_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein phosphatase non-receptor type 6 measurement http://www.ebi.ac.uk/efo/EFO_0020837 GCST90237622 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein amnionless level in Chronic kidney disease with hypertension and no diabetes (4322_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein amnionless measurement http://www.ebi.ac.uk/efo/EFO_0020667 GCST90237623 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin-SA level in Chronic kidney disease with hypertension and no diabetes (4324_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin-SA measurement http://www.ebi.ac.uk/efo/EFO_0008105 GCST90237624 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brother of CDO level in Chronic kidney disease with hypertension and no diabetes (4328_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 brother of CDO measurement http://www.ebi.ac.uk/efo/EFO_0020194 GCST90237625 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostate-specific antigen level in Chronic kidney disease with hypertension and no diabetes (4330_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST90237626 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin subfamily 2 member A2 level in Chronic kidney disease with hypertension and no diabetes (22586_24) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of butyrophilin subfamily 2 member A2 in blood serum http://purl.obolibrary.org/obo/OBA_2044701 GCST90236137 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 6 level in Chronic kidney disease with hypertension and no diabetes (22587_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ephrin type-A receptor 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041490 GCST90236138 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G protein-coupled receptor B2 level in Chronic kidney disease with hypertension and no diabetes (22588_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adhesion G protein-coupled receptor B2 in blood serum http://purl.obolibrary.org/obo/OBA_2040773 GCST90236139 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-2 level in Chronic kidney disease with hypertension and no diabetes (22589_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frizzled-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041640 GCST90236140 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-1 level in Chronic kidney disease with hypertension and no diabetes (22590_68) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of frizzled-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041639 GCST90236141 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-9 level in Chronic kidney disease with hypertension and no diabetes (22591_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frizzled-9 in blood serum http://purl.obolibrary.org/obo/OBA_2040302 GCST90236142 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Solute carrier family 25 member 38 level in Chronic kidney disease with hypertension and no diabetes (22770_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial glycine transporter in blood serum http://purl.obolibrary.org/obo/OBA_2044469 GCST90236143 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sterile alpha motif domain-containing protein 12 level in Chronic kidney disease with hypertension and no diabetes (22771_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sterile alpha motif domain-containing protein 12 in blood serum http://purl.obolibrary.org/obo/OBA_2044607 GCST90236144 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting and assembly machinery component 50 homolog level in Chronic kidney disease with hypertension and no diabetes (22772_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting and assembly machinery component 50 in blood serum http://purl.obolibrary.org/obo/OBA_2043376 GCST90236145 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22773_69) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043415 GCST90236146 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA-splicing endonuclease subunit Sen34 level in Chronic kidney disease with hypertension and no diabetes (22774_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA-splicing endonuclease subunit Sen34 in blood serum http://purl.obolibrary.org/obo/OBA_2043946 GCST90236147 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-phase kinase-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (22777_46) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of S-phase kinase-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043520 GCST90236148 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Single-pass membrane and coiled-coil domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (22779_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of single-pass membrane and coiled-coil domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044825 GCST90236149 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinetochore protein Spc25 level in Chronic kidney disease with hypertension and no diabetes (22782_80) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of kinetochore protein Spc25 in blood serum http://purl.obolibrary.org/obo/OBA_2043621 GCST90236150 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor PU.1 level in Chronic kidney disease with hypertension and no diabetes (22783_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor PU.1 in blood serum http://purl.obolibrary.org/obo/OBA_2040360 GCST90236151 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermatogenesis-associated protein 22 level in Chronic kidney disease with hypertension and no diabetes (22784_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spermatogenesis-associated protein 22 in blood serum http://purl.obolibrary.org/obo/OBA_2043618 GCST90236152 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermatogenesis-associated protein 46 level in Chronic kidney disease with hypertension and no diabetes (22786_57) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of spermatogenesis-associated protein 46 in blood serum http://purl.obolibrary.org/obo/OBA_2044829 GCST90236153 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm protein associated with the nucleus on the X chromosome N3 level in Chronic kidney disease with hypertension and no diabetes (22787_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm protein associated with the nucleus on the X chromosome N3 in blood serum http://purl.obolibrary.org/obo/OBA_2043615 GCST90236154 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfotransferase 6B1 level in Chronic kidney disease with hypertension and no diabetes (22788_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 6B1 in blood serum http://purl.obolibrary.org/obo/OBA_2043731 GCST90236155 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metalloproteinase inhibitor 2 level in Chronic kidney disease with hypertension and no diabetes (2278_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 metalloproteinase inhibitor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020567 GCST90236156 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptophan--tRNA ligase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22792_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tryptophan--tRNA ligase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044123 GCST90236157 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription initiation factor IIA subunit 2 level in Chronic kidney disease with hypertension and no diabetes (22793_110) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transcription initiation factor IIA subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041812 GCST90236158 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional adapter 2-alpha level in Chronic kidney disease with hypertension and no diabetes (22795_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional adapter 2-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043767 GCST90236159 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional adapter 1 level in Chronic kidney disease with hypertension and no diabetes (22796_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional adapter 1-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2043766 GCST90236160 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription initiation factor TFIID subunit 12 level in Chronic kidney disease with hypertension and no diabetes (22797_20) 466 African American individuals NA Illumina [14870897] (imputed) 3 level of transcription initiation factor TFIID subunit 12 in blood serum http://purl.obolibrary.org/obo/OBA_2043770 GCST90236161 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynein light chain 2, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (11493_169) 466 African American individuals NA Illumina [14870897] (imputed) 0 dynein light chain 1, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0020339 GCST90233271 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA polymerase II elongation factor ELL2 level in Chronic kidney disease with hypertension and no diabetes (11494_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of RNA polymerase II elongation factor ELL2 in blood serum http://purl.obolibrary.org/obo/OBA_2041470 GCST90233272 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein L1 level in Chronic kidney disease with hypertension and no diabetes (11510_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90233273 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein L1 level in Chronic kidney disease with hypertension and no diabetes (11510_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90233274 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (11513_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021923 GCST90233275 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD59 glycoprotein level in Chronic kidney disease with hypertension and no diabetes (11514_196) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD59 glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0021924 GCST90233276 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein, liver level in Chronic kidney disease with hypertension and no diabetes (11516_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 fatty acid-binding protein, liver measurement http://www.ebi.ac.uk/efo/EFO_0021855 GCST90233277 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Porphobilinogen deaminase level in Chronic kidney disease with hypertension and no diabetes (11530_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of porphobilinogen deaminase in blood serum http://purl.obolibrary.org/obo/OBA_2041884 GCST90233278 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-type immunoglobulin domain-containing suppressor of T-cell activation level in Chronic kidney disease with hypertension and no diabetes (11531_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233279 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (11534_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044515 GCST90233280 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H2A deubiquitinase MYSM1 level in Chronic kidney disease with hypertension and no diabetes (11536_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deubiquitinase MYSM1 in blood serum http://purl.obolibrary.org/obo/OBA_2042491 GCST90233281 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transferrin receptor protein 2 level in Chronic kidney disease with hypertension and no diabetes (11537_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transferrin receptor protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043834 GCST90233282 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Malonyl-CoA decarboxylase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11538_216) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of malonyl-CoA decarboxylase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042382 GCST90233283 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP synthase subunit f, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11539_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP synthase subunit f, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040731 GCST90233284 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein O3 level in Chronic kidney disease with hypertension and no diabetes (11540_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein O3 in blood serum http://purl.obolibrary.org/obo/OBA_2041611 GCST90233285 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 230 level in Chronic kidney disease with hypertension and no diabetes (11542_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 230 in blood serum http://purl.obolibrary.org/obo/OBA_2044422 GCST90233286 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain and actin-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (11543_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LIM domain and actin-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042202 GCST90233287 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PHD finger protein 3 level in Chronic kidney disease with hypertension and no diabetes (11544_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PHD finger protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042873 GCST90233288 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 14 level in Chronic kidney disease with hypertension and no diabetes (11545_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0020805 GCST90233289 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoglobin level in Chronic kidney disease with hypertension and no diabetes (11546_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytoglobin in blood serum http://purl.obolibrary.org/obo/OBA_2041214 GCST90233290 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Muscle, skeletal receptor tyrosine-protein kinase level in Chronic kidney disease with hypertension and no diabetes (11547_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of muscle, skeletal receptor tyrosine-protein kinase in blood serum http://purl.obolibrary.org/obo/OBA_2042463 GCST90233291 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. M-phase inducer phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (11548_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of M-phase inducer phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040950 GCST90233292 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin gene enhancer protein ISL-1 level in Chronic kidney disease with hypertension and no diabetes (11549_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin gene enhancer protein ISL-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042043 GCST90233293 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related level in Chronic kidney disease with hypertension and no diabetes (11551_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related in blood serum http://purl.obolibrary.org/obo/OBA_2041886 GCST90233294 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor GTPase-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (11556_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor GTPase-activating protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040644 GCST90233295 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TBC1 domain family member 28 level in Chronic kidney disease with hypertension and no diabetes (22799_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TBC1 domain family member 28 in blood serum http://purl.obolibrary.org/obo/OBA_2044573 GCST90236162 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Telethonin level in Chronic kidney disease with hypertension and no diabetes (22800_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of telethonin in blood serum http://purl.obolibrary.org/obo/OBA_2043800 GCST90236163 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Telomere repeats-binding bouquet formation protein 2 level in Chronic kidney disease with hypertension and no diabetes (22801_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of telomere repeats-binding bouquet formation protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044848 GCST90236164 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testis-expressed protein 30 level in Chronic kidney disease with hypertension and no diabetes (22802_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of testis-expressed protein 30 in blood serum http://purl.obolibrary.org/obo/OBA_2044604 GCST90236165 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. THAP domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (22806_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of THAP domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044364 GCST90236166 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyroid hormone receptor beta level in Chronic kidney disease with hypertension and no diabetes (22808_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thyroid hormone receptor beta in blood serum http://purl.obolibrary.org/obo/OBA_2043844 GCST90236167 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit Tim23 level in Chronic kidney disease with hypertension and no diabetes (22809_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import inner membrane translocase subunit Tim23 in blood serum http://purl.obolibrary.org/obo/OBA_2043854 GCST90236168 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TIMELESS-interacting protein level in Chronic kidney disease with hypertension and no diabetes (22810_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TIMELESS-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043859 GCST90236169 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translation machinery-associated protein 16 level in Chronic kidney disease with hypertension and no diabetes (22811_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of translation machinery-associated protein 16 in blood serum http://purl.obolibrary.org/obo/OBA_2044750 GCST90236170 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trafficking protein particle complex subunit 6B level in Chronic kidney disease with hypertension and no diabetes (22812_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trafficking protein particle complex subunit 6B in blood serum http://purl.obolibrary.org/obo/OBA_2043923 GCST90236171 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TPT1-like protein level in Chronic kidney disease with hypertension and no diabetes (22813_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of TPT1-like protein (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044904 GCST90236172 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein RFP level in Chronic kidney disease with hypertension and no diabetes (22814_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein RFP in blood serum http://purl.obolibrary.org/obo/OBA_2043934 GCST90236173 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tripartite motif-containing protein 40 level in Chronic kidney disease with hypertension and no diabetes (22815_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin ligase TRIM40 in blood serum http://purl.obolibrary.org/obo/OBA_2044372 GCST90236174 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tripartite motif-containing protein 54 level in Chronic kidney disease with hypertension and no diabetes (22816_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tripartite motif-containing protein 54 in blood serum http://purl.obolibrary.org/obo/OBA_2043936 GCST90236175 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase TRIM9 level in Chronic kidney disease with hypertension and no diabetes (22817_126) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase TRIM9 in blood serum http://purl.obolibrary.org/obo/OBA_2043938 GCST90236176 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tricarboxylate transport protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22818_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tricarboxylate transport protein, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043528 GCST90236177 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uracil-DNA glycosylase level in Chronic kidney disease with hypertension and no diabetes (22821_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of uracil-DNA glycosylase in blood serum http://purl.obolibrary.org/obo/OBA_2044040 GCST90236178 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-type proton ATPase subunit C 2 level in Chronic kidney disease with hypertension and no diabetes (22824_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-type proton ATPase subunit C 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040734 GCST90236179 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Von Hippel-Lindau-like protein level in Chronic kidney disease with hypertension and no diabetes (22826_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of von Hippel-Lindau-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2044098 GCST90236180 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Z-DNA-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (22831_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Z-DNA-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044170 GCST90236181 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger CCCH domain-containing protein 8 level in Chronic kidney disease with hypertension and no diabetes (22832_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger CCCH domain-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044381 GCST90236182 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger CCHC domain-containing protein 18 level in Chronic kidney disease with hypertension and no diabetes (22833_74) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of zinc finger CCHC domain-containing protein 18 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044897 GCST90236183 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable palmitoyltransferase ZDHHC4 level in Chronic kidney disease with hypertension and no diabetes (22834_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of palmitoyltransferase ZDHHC4 in blood serum http://purl.obolibrary.org/obo/OBA_2044459 GCST90236184 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 230 level in Chronic kidney disease with hypertension and no diabetes (22838_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 230 in blood serum http://purl.obolibrary.org/obo/OBA_2044195 GCST90236185 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 263 level in Chronic kidney disease with hypertension and no diabetes (22839_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 263 in blood serum http://purl.obolibrary.org/obo/OBA_2044196 GCST90236186 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcineurin level in Chronic kidney disease with hypertension and no diabetes (4903_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcineurin measurement http://www.ebi.ac.uk/efo/EFO_0008061 GCST90237737 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-2 level in Chronic kidney disease with hypertension and no diabetes (4904_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 caspase-2 measurement http://www.ebi.ac.uk/efo/EFO_0020240 GCST90237738 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coactosin-like protein level in Chronic kidney disease with hypertension and no diabetes (4905_63) 466 African American individuals NA Illumina [14870897] (imputed) 1 coactosin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020262 GCST90237739 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoglin level in Chronic kidney disease with hypertension and no diabetes (4908_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 endoglin measurement http://www.ebi.ac.uk/efo/EFO_0008118 GCST90237740 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-8 level in Chronic kidney disease with hypertension and no diabetes (4909_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-8 measurement http://www.ebi.ac.uk/efo/EFO_0020399 GCST90237741 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Suppressor of cytokine signaling 3 level in Chronic kidney disease with hypertension and no diabetes (11440_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of suppressor of cytokine signaling 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043592 GCST90233251 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycogen phosphorylase, liver form level in Chronic kidney disease with hypertension and no diabetes (11441_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycogen phosphorylase, liver form in blood serum http://purl.obolibrary.org/obo/OBA_2043126 GCST90233252 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta and Notch-like epidermal growth factor-related receptor level in Chronic kidney disease with hypertension and no diabetes (11442_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233253 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerase III subunit RPC6 level in Chronic kidney disease with hypertension and no diabetes (11444_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerase III subunit RPC6 in blood serum http://purl.obolibrary.org/obo/OBA_2042972 GCST90233254 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galactokinase level in Chronic kidney disease with hypertension and no diabetes (11448_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of galactokinase in blood serum http://purl.obolibrary.org/obo/OBA_2041656 GCST90233255 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase level in Chronic kidney disease with hypertension and no diabetes (11450_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein disulfide-isomerase measurement http://www.ebi.ac.uk/efo/EFO_0020669 GCST90233256 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 3 subunit G level in Chronic kidney disease with hypertension and no diabetes (11454_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 3 subunit G in blood serum http://purl.obolibrary.org/obo/OBA_2041447 GCST90233257 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen B10 level in Chronic kidney disease with hypertension and no diabetes (11456_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen B10 in blood serum http://purl.obolibrary.org/obo/OBA_2042270 GCST90233258 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly(rC)-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (11458_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of poly(rC)-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042779 GCST90233259 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA polymerase II elongation factor ELL level in Chronic kidney disease with hypertension and no diabetes (11459_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA polymerase II elongation factor ELL in blood serum http://purl.obolibrary.org/obo/OBA_2041469 GCST90233260 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA binding protein fox-1 homolog 2 level in Chronic kidney disease with hypertension and no diabetes (11462_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA binding protein fox-1 homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043209 GCST90233261 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor RelB level in Chronic kidney disease with hypertension and no diabetes (11464_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor RelB in blood serum http://purl.obolibrary.org/obo/OBA_2043234 GCST90233262 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable G-protein coupled receptor 135 level in Chronic kidney disease with hypertension and no diabetes (11465_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of G-protein coupled receptor 135 in blood serum http://purl.obolibrary.org/obo/OBA_2040307 GCST90233263 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable RNA-binding protein 19 level in Chronic kidney disease with hypertension and no diabetes (11468_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable RNA-binding protein 19 in blood serum http://purl.obolibrary.org/obo/OBA_2044624 GCST90233264 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein sorting-associated protein 4A level in Chronic kidney disease with hypertension and no diabetes (11476_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vacuolar protein sorting-associated protein 4A in blood serum http://purl.obolibrary.org/obo/OBA_2044111 GCST90233265 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldehyde dehydrogenase, dimeric NADP-preferring level in Chronic kidney disease with hypertension and no diabetes (11480_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldehyde dehydrogenase, dimeric NADP-preferring in blood serum http://purl.obolibrary.org/obo/OBA_2040563 GCST90233266 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatitis A virus cellular receptor 2 level in Chronic kidney disease with hypertension and no diabetes (11481_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90233267 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 174 level in Chronic kidney disease with hypertension and no diabetes (11486_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 174 in blood serum http://purl.obolibrary.org/obo/OBA_2044190 GCST90233268 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testican-1 level in Chronic kidney disease with hypertension and no diabetes (11487_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 testican-1 measurement http://www.ebi.ac.uk/efo/EFO_0020765 GCST90233269 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like protein 4A level in Chronic kidney disease with hypertension and no diabetes (11490_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like protein 4A in blood serum http://purl.obolibrary.org/obo/OBA_2044009 GCST90233270 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase SMURF1 level in Chronic kidney disease with hypertension and no diabetes (11557_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase SMURF1 in blood serum http://purl.obolibrary.org/obo/OBA_2040214 GCST90233296 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear factor of activated T-cells, cytoplasmic 4 level in Chronic kidney disease with hypertension and no diabetes (11560_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear factor of activated T-cells, cytoplasmic 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042569 GCST90233297 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA polymerase epsilon subunit 2 level in Chronic kidney disease with hypertension and no diabetes (11562_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA polymerase epsilon subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042961 GCST90233298 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (11563_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233299 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 23 level in Chronic kidney disease with hypertension and no diabetes (11565_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 23 in blood serum http://purl.obolibrary.org/obo/OBA_2044194 GCST90233300 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type II cytoskeletal 72 level in Chronic kidney disease with hypertension and no diabetes (11566_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type II cytoskeletal 72 in blood serum http://purl.obolibrary.org/obo/OBA_2042148 GCST90233301 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 10 level in Chronic kidney disease with hypertension and no diabetes (11567_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044187 GCST90233302 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase FKBP1B level in Chronic kidney disease with hypertension and no diabetes (11568_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase FKBP1B in blood serum http://purl.obolibrary.org/obo/OBA_2041588 GCST90233303 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell receptor-associated protein 29 level in Chronic kidney disease with hypertension and no diabetes (11570_94) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell receptor-associated protein 29 in blood serum http://purl.obolibrary.org/obo/OBA_2040783 GCST90233304 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2-E type II integral membrane protein level in Chronic kidney disease with hypertension and no diabetes (11571_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233305 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynamin-2 level in Chronic kidney disease with hypertension and no diabetes (11572_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynamin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041336 GCST90233306 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/arginine-rich splicing factor 6 level in Chronic kidney disease with hypertension and no diabetes (11573_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/arginine-rich splicing factor 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043479 GCST90233307 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily A member 2 level in Chronic kidney disease with hypertension and no diabetes (11582_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily A member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041326 GCST90233308 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat neuronal protein 1 level in Chronic kidney disease with hypertension and no diabetes (11586_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233309 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAX gene-associated protein level in Chronic kidney disease with hypertension and no diabetes (11587_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MAX gene-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2042355 GCST90233310 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable RNA-binding protein 23 level in Chronic kidney disease with hypertension and no diabetes (11590_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable RNA-binding protein 23 in blood serum http://purl.obolibrary.org/obo/OBA_2044351 GCST90233311 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein regulator of cytokinesis 1 level in Chronic kidney disease with hypertension and no diabetes (11591_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein regulator of cytokinesis 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043017 GCST90233312 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ELAV-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (11592_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ELAV-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041463 GCST90233313 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 9 level in Chronic kidney disease with hypertension and no diabetes (11593_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-X-C motif chemokine 9 measurement http://www.ebi.ac.uk/efo/EFO_0022032 GCST90233314 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 75D level in Chronic kidney disease with hypertension and no diabetes (11596_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 75D in blood serum http://purl.obolibrary.org/obo/OBA_2044214 GCST90233315 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent RNA helicase DHX8 level in Chronic kidney disease with hypertension and no diabetes (11601_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent RNA helicase DHX8 in blood serum http://purl.obolibrary.org/obo/OBA_2041299 GCST90233316 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Copine-1 level in Chronic kidney disease with hypertension and no diabetes (11602_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90233317 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 6 level in Chronic kidney disease with hypertension and no diabetes (11606_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041328 GCST90233318 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bromodomain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (11607_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bromodomain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044256 GCST90233319 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated proteins 1A/1B light chain 3B level in Chronic kidney disease with hypertension and no diabetes (11608_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated proteins 1A/1B light chain 3B in blood serum http://purl.obolibrary.org/obo/OBA_2042283 GCST90233320 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 696 level in Chronic kidney disease with hypertension and no diabetes (22841_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 696 in blood serum http://purl.obolibrary.org/obo/OBA_2044213 GCST90236187 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 69 level in Chronic kidney disease with hypertension and no diabetes (22842_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 69 in blood serum http://purl.obolibrary.org/obo/OBA_2044212 GCST90236188 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger SWIM domain-containing protein 7 level in Chronic kidney disease with hypertension and no diabetes (22844_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger SWIM domain-containing protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044221 GCST90236189 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 28S ribosomal protein S14, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (22845_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 28S ribosomal protein S14, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042434 GCST90236190 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase 4 level in Chronic kidney disease with hypertension and no diabetes (22847_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043700 GCST90236191 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD7 level in Chronic kidney disease with hypertension and no diabetes (22857_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD7 in blood serum http://purl.obolibrary.org/obo/OBA_2044321 GCST90236192 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 6 level in Chronic kidney disease with hypertension and no diabetes (22858_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042294 GCST90236193 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1M level in Chronic kidney disease with hypertension and no diabetes (22862_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1M in blood serum http://purl.obolibrary.org/obo/OBA_2042997 GCST90236194 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleotide pyrophosphatase/phosphodiesterase family member 7 level in Chronic kidney disease with hypertension and no diabetes (4435_66) 466 African American individuals NA Illumina [14870897] (imputed) 1 ectonucleotide pyrophosphatase/phosphodiesterase family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0020344 GCST90237645 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleoside triphosphate diphosphohydrolase 3 level in Chronic kidney disease with hypertension and no diabetes (4436_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 ectonucleoside triphosphate diphosphohydrolase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020343 GCST90237646 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleoside triphosphate diphosphohydrolase 5 level in Chronic kidney disease with hypertension and no diabetes (4437_56) 466 African American individuals NA Illumina [14870897] (imputed) 1 ectonucleoside triphosphate diphosphohydrolase 5 measurement http://www.ebi.ac.uk/efo/EFO_0008115 GCST90237647 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fc receptor-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (4440_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 Fc receptor-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008127 GCST90237648 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein A/B level in Chronic kidney disease with hypertension and no diabetes (4450_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 heterogeneous nuclear ribonucleoprotein a/b measurement http://www.ebi.ac.uk/efo/EFO_0020441 GCST90237649 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane neuronal protein 1 level in Chronic kidney disease with hypertension and no diabetes (4452_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine-rich repeat transmembrane neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020531 GCST90237650 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane neuronal protein 3 level in Chronic kidney disease with hypertension and no diabetes (4453_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine-rich repeat transmembrane neuronal protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020532 GCST90237651 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactadherin level in Chronic kidney disease with hypertension and no diabetes (4455_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 lactadherin measurement http://www.ebi.ac.uk/efo/EFO_0008203 GCST90237652 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proprotein convertase subtilisin/kexin type 7 level in Chronic kidney disease with hypertension and no diabetes (4459_68) 466 African American individuals NA Illumina [14870897] (imputed) 1 proprotein convertase subtilisin/kexin type 7 measurement http://www.ebi.ac.uk/efo/EFO_0008270 GCST90237653 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-phosphoinositide-dependent protein kinase 1 level in Chronic kidney disease with hypertension and no diabetes (4460_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 3-phosphoinositide-dependent protein kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020116 GCST90237654 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialoadhesin level in Chronic kidney disease with hypertension and no diabetes (4464_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 sialoadhesin measurement http://www.ebi.ac.uk/efo/EFO_0020740 GCST90237655 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPARC-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (4467_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 SPARC-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008289 GCST90237656 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sphingosine kinase 2 level in Chronic kidney disease with hypertension and no diabetes (4468_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 sphingosine kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020751 GCST90237657 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 15 level in Chronic kidney disease with hypertension and no diabetes (4469_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbohydrate sulfotransferase 15 measurement http://www.ebi.ac.uk/efo/EFO_0008066 GCST90237658 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plasma protease C1 inhibitor level in Chronic kidney disease with hypertension and no diabetes (4479_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 plasma protease C1 inhibitor measurement http://www.ebi.ac.uk/efo/EFO_0008261 GCST90237659 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C3b level in Chronic kidney disease with hypertension and no diabetes (4480_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C3B measurement http://www.ebi.ac.uk/efo/EFO_0020275 GCST90237660 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C4 level in Chronic kidney disease with hypertension and no diabetes (4481_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C4 measurement http://www.ebi.ac.uk/efo/EFO_0004984 GCST90237661 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C5b-C6 complex level in Chronic kidney disease with hypertension and no diabetes (4482_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C5B-C6 complex measurement http://www.ebi.ac.uk/efo/EFO_0020279 GCST90237662 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 7 level in Chronic kidney disease with hypertension and no diabetes (4487_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 7 measurement http://www.ebi.ac.uk/efo/EFO_0020384 GCST90237663 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-5 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (4491_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin 5 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0008186 GCST90237664 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-11 level in Chronic kidney disease with hypertension and no diabetes (4493_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-11 measurement http://www.ebi.ac.uk/efo/EFO_0020490 GCST90237665 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage metalloelastase level in Chronic kidney disease with hypertension and no diabetes (4496_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage metalloelastase measurement http://www.ebi.ac.uk/efo/EFO_0008220 GCST90237666 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neural cell adhesion molecule 1, 120 kDa isoform level in Chronic kidney disease with hypertension and no diabetes (4498_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 neural cell adhesion molecule 1, 120 kda isoform measurement http://www.ebi.ac.uk/efo/EFO_0020593 GCST90237667 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor subunit A level in Chronic kidney disease with hypertension and no diabetes (4499_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of platelet-derived growth factor subunit A in blood serum http://purl.obolibrary.org/obo/OBA_2042824 GCST90237668 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stem cell growth factor-alpha level in Chronic kidney disease with hypertension and no diabetes (4500_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 stem cell growth factor-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020754 GCST90237669 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A disintegrin and metalloproteinase with thrombospondin motifs 15 level in Chronic kidney disease with hypertension and no diabetes (4533_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 a disintegrin and metalloproteinase with thrombospondin motifs 15 measurement http://www.ebi.ac.uk/efo/EFO_0020123 GCST90237670 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brain-specific serine protease 4 level in Chronic kidney disease with hypertension and no diabetes (4534_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 brain-specific serine protease 4 measurement http://www.ebi.ac.uk/efo/EFO_0020192 GCST90237671 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 level in Chronic kidney disease with hypertension and no diabetes (4535_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008014 GCST90237672 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromobox protein homolog 5 level in Chronic kidney disease with hypertension and no diabetes (4540_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 chromobox protein homolog 5 measurement http://www.ebi.ac.uk/efo/EFO_0020258 GCST90237673 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell adhesion molecule-related/down-regulated by oncogenes level in Chronic kidney disease with hypertension and no diabetes (4541_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 cell adhesion molecule-related/down-regulated by oncogenes measurement http://www.ebi.ac.uk/efo/EFO_0008079 GCST90237674 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Clusterin level in Chronic kidney disease with hypertension and no diabetes (4542_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 clusterin measurement http://www.ebi.ac.uk/efo/EFO_0007655 GCST90237675 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(XXIII) chain level in Chronic kidney disease with hypertension and no diabetes (4543_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 collagen alpha-1(XXIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020270 GCST90237676 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit TIM14 level in Chronic kidney disease with hypertension and no diabetes (4545_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitochondrial import inner membrane translocase subunit tim14 measurement http://www.ebi.ac.uk/efo/EFO_0020573 GCST90237677 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G protein-coupled receptor E2 level in Chronic kidney disease with hypertension and no diabetes (4546_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 adhesion G protein-coupled receptor E2 measurement http://www.ebi.ac.uk/efo/EFO_0021892 GCST90237678 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane protein FLRT1 level in Chronic kidney disease with hypertension and no diabetes (4547_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine-rich repeat transmembrane protein FLRT1 measurement http://www.ebi.ac.uk/efo/EFO_0020533 GCST90237679 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galactoside 3(4)-L-fucosyltransferase level in Chronic kidney disease with hypertension and no diabetes (4548_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 galactoside 3(4)-L-fucosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0021853 GCST90237680 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-(1,3)-fucosyltransferase 5 level in Chronic kidney disease with hypertension and no diabetes (4549_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha-(1,3)-fucosyltransferase 5 measurement http://www.ebi.ac.uk/efo/EFO_0020136 GCST90237681 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G-protein coupled receptor G5 level in Chronic kidney disease with hypertension and no diabetes (4551_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 adhesion G-protein coupled receptor G5 measurement http://www.ebi.ac.uk/efo/EFO_0021980 GCST90237682 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatoma-derived growth factor-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (4553_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 hepatoma-derived growth factor-related protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020439 GCST90237683 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-34 level in Chronic kidney disease with hypertension and no diabetes (4556_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 interleukin-34 measurement http://www.ebi.ac.uk/efo/EFO_0020505 GCST90237684 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kin of IRRE-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (4557_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 kin of IRRE-like protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020521 GCST90237685 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kynureninase level in Chronic kidney disease with hypertension and no diabetes (4559_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 kynureninase measurement http://www.ebi.ac.uk/efo/EFO_0008201 GCST90237686 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 level in Chronic kidney disease with hypertension and no diabetes (4563_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1 measurement http://www.ebi.ac.uk/efo/EFO_0020108 GCST90237687 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin-C1 level in Chronic kidney disease with hypertension and no diabetes (4564_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 plexin-C1 measurement http://www.ebi.ac.uk/efo/EFO_0008266 GCST90237688 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. R-spondin-2 level in Chronic kidney disease with hypertension and no diabetes (4566_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 r-spondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020696 GCST90237689 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH2 domain-containing protein 1A level in Chronic kidney disease with hypertension and no diabetes (4567_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 sh2 domain-containing protein 1a measurement http://www.ebi.ac.uk/efo/EFO_0020737 GCST90237690 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT and NTRK-like protein 5 level in Chronic kidney disease with hypertension and no diabetes (4568_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 slit and ntrk-like protein 5 measurement http://www.ebi.ac.uk/efo/EFO_0020743 GCST90237691 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. VPS10 domain-containing receptor SorCS2 level in Chronic kidney disease with hypertension and no diabetes (4569_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 vps10 domain-containing receptor sorcs2 measurement http://www.ebi.ac.uk/efo/EFO_0020851 GCST90237692 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pancreatic hormone level in Chronic kidney disease with hypertension and no diabetes (4588_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 pancreatic hormone measurement http://www.ebi.ac.uk/efo/EFO_0020621 GCST90237693 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pituitary adenylate cyclase-activating polypeptide 38 level in Chronic kidney disease with hypertension and no diabetes (4594_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 pituitary adenylate cyclase-activating polypeptide 38 measurement http://www.ebi.ac.uk/efo/EFO_0020641 GCST90237694 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-6 level in Chronic kidney disease with hypertension and no diabetes (4673_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-6 measurement http://www.ebi.ac.uk/efo/EFO_0004810 GCST90237695 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-hydroxyisobutyrate dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (4693_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 3-hydroxyisobutyrate dehydrogenase, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020115 GCST90237696 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein, heart level in Chronic kidney disease with hypertension and no diabetes (4696_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 fatty acid-binding protein, heart measurement http://www.ebi.ac.uk/efo/EFO_0020373 GCST90237697 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulocyte-macrophage colony-stimulating factor level in Chronic kidney disease with hypertension and no diabetes (4697_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 granulocyte-macrophage colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0020417 GCST90237698 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphotoxin-alpha level in Chronic kidney disease with hypertension and no diabetes (4703_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphotoxin-alpha measurement http://www.ebi.ac.uk/efo/EFO_0020544 GCST90237699 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein 4.1 level in Chronic kidney disease with hypertension and no diabetes (4706_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein 4.1 in blood serum http://purl.obolibrary.org/obo/OBA_2041485 GCST90237700 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein eta level in Chronic kidney disease with hypertension and no diabetes (4707_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 14-3-3 protein eta in blood serum http://purl.obolibrary.org/obo/OBA_2044167 GCST90237701 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein D level in Chronic kidney disease with hypertension and no diabetes (4712_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90237702 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-3 level in Chronic kidney disease with hypertension and no diabetes (4717_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020503 GCST90237703 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase B level in Chronic kidney disease with hypertension and no diabetes (4718_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptidyl-prolyl cis-trans isomerase B measurement http://www.ebi.ac.uk/efo/EFO_0020626 GCST90237704 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase A3 level in Chronic kidney disease with hypertension and no diabetes (4719_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein disulfide-isomerase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020668 GCST90237705 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trefoil factor 3 level in Chronic kidney disease with hypertension and no diabetes (4721_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90237706 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Afamin level in Chronic kidney disease with hypertension and no diabetes (4763_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 afamin measurement http://www.ebi.ac.uk/efo/EFO_0008015 GCST90237707 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Olfactomedin-4 level in Chronic kidney disease with hypertension and no diabetes (4769_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 olfactomedin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020617 GCST90237708 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acid sphingomyelinase-like phosphodiesterase 3a level in Chronic kidney disease with hypertension and no diabetes (4771_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 acid sphingomyelinase-like phosphodiesterase 3a measurement http://www.ebi.ac.uk/efo/EFO_0008013 GCST90237709 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gelsolin level in Chronic kidney disease with hypertension and no diabetes (4775_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 gelsolin measurement http://www.ebi.ac.uk/efo/EFO_0020402 GCST90237710 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Corticosteroid-binding globulin level in Chronic kidney disease with hypertension and no diabetes (4785_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 corticosteroid-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0020288 GCST90237711 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactoperoxidase level in Chronic kidney disease with hypertension and no diabetes (4801_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 lactoperoxidase measurement http://www.ebi.ac.uk/efo/EFO_0020525 GCST90237712 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(VIII) chain level in Chronic kidney disease with hypertension and no diabetes (4807_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 collagen alpha-1(VIII) chain measurement http://www.ebi.ac.uk/efo/EFO_0020269 GCST90237713 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inter-alpha-trypsin inhibitor heavy chain H4 level in Chronic kidney disease with hypertension and no diabetes (4811_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 inter-alpha-trypsin inhibitor heavy chain h4 measurement http://www.ebi.ac.uk/efo/EFO_0020481 GCST90237714 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin domain-containing protein 12 level in Chronic kidney disease with hypertension and no diabetes (4815_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90237715 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein sigma level in Chronic kidney disease with hypertension and no diabetes (4829_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 14-3-3 protein sigma measurement http://www.ebi.ac.uk/efo/EFO_0020110 GCST90237716 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. L-Selectin level in Chronic kidney disease with hypertension and no diabetes (4831_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 L-Selectin measurement http://www.ebi.ac.uk/efo/EFO_0008202 GCST90237717 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 10A level in Chronic kidney disease with hypertension and no diabetes (4832_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 10A measurement http://www.ebi.ac.uk/efo/EFO_0020799 GCST90237718 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 2 level in Chronic kidney disease with hypertension and no diabetes (4834_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-a receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020351 GCST90237719 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulocyte colony-stimulating factor level in Chronic kidney disease with hypertension and no diabetes (4840_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90237720 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glypican-3 level in Chronic kidney disease with hypertension and no diabetes (4842_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 glypican-3 measurement http://www.ebi.ac.uk/efo/EFO_0020415 GCST90237721 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 alpha level in Chronic kidney disease with hypertension and no diabetes (4851_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-1 alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040246 GCST90237722 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein receptor type-1A level in Chronic kidney disease with hypertension and no diabetes (4859_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 bone morphogenetic protein receptor type-1a measurement http://www.ebi.ac.uk/efo/EFO_0020188 GCST90237723 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein receptor type-2 level in Chronic kidney disease with hypertension and no diabetes (4862_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 bone morphogenetic protein receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020189 GCST90237724 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BDNF/NT-3 growth factors receptor level in Chronic kidney disease with hypertension and no diabetes (4866_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 bdnf/nt-3 growth factors receptor measurement http://www.ebi.ac.uk/efo/EFO_0020179 GCST90237725 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor A, isoform 121 level in Chronic kidney disease with hypertension and no diabetes (4867_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 vascular endothelial growth factor A, isoform 121 measurement http://www.ebi.ac.uk/efo/EFO_0020847 GCST90237726 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiogenin level in Chronic kidney disease with hypertension and no diabetes (4874_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiogenin measurement http://www.ebi.ac.uk/efo/EFO_0008022 GCST90237727 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation factor IX level in Chronic kidney disease with hypertension and no diabetes (4876_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 coagulation factor IX measurement http://www.ebi.ac.uk/efo/EFO_0020263 GCST90237728 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation Factor X level in Chronic kidney disease with hypertension and no diabetes (4878_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 coagulation factor X measurement http://www.ebi.ac.uk/efo/EFO_0020265 GCST90237729 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 2 level in Chronic kidney disease with hypertension and no diabetes (4880_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 growth/differentiation factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0020428 GCST90237730 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin level in Chronic kidney disease with hypertension and no diabetes (4883_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin measurement http://www.ebi.ac.uk/efo/EFO_0004467 GCST90237731 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 7 level in Chronic kidney disease with hypertension and no diabetes (4886_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST90237732 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-7a level in Chronic kidney disease with hypertension and no diabetes (4889_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein wnt-7a measurement http://www.ebi.ac.uk/efo/EFO_0020689 GCST90237733 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Corticotropin level in Chronic kidney disease with hypertension and no diabetes (4890_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 corticotropin measurement http://www.ebi.ac.uk/efo/EFO_0020289 GCST90237734 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucagon level in Chronic kidney disease with hypertension and no diabetes (4891_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 glucagon measurement http://www.ebi.ac.uk/efo/EFO_0008463 GCST90237735 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C3a anaphylatoxin level in Chronic kidney disease with hypertension and no diabetes (4900_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 C3a anaphylatoxin measurement http://www.ebi.ac.uk/efo/EFO_0020207 GCST90237736 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histamine N-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (23178_95) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of histamine N-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041902 GCST90236252 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte tyrosine kinase receptor level in Chronic kidney disease with hypertension and no diabetes (23181_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte tyrosine kinase receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042246 GCST90236253 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF31 level in Chronic kidney disease with hypertension and no diabetes (23183_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RNF31 in blood serum http://purl.obolibrary.org/obo/OBA_2043297 GCST90236254 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deubiquitinating protein VCIP135 level in Chronic kidney disease with hypertension and no diabetes (23187_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deubiquitinating protein VCPIP1 in blood serum http://purl.obolibrary.org/obo/OBA_2044091 GCST90236255 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q tumor necrosis factor-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (23200_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q tumor necrosis factor-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040851 GCST90236256 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ecto-ADP-ribosyltransferase 5 level in Chronic kidney disease with hypertension and no diabetes (23202_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ecto-ADP-ribosyltransferase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040393 GCST90236257 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ETS translocation variant 2 level in Chronic kidney disease with hypertension and no diabetes (23210_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ETS translocation variant 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041518 GCST90236258 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein EURL homolog level in Chronic kidney disease with hypertension and no diabetes (23212_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein EURL in blood serum http://purl.obolibrary.org/obo/OBA_2041520 GCST90236259 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C11orf70 level in Chronic kidney disease with hypertension and no diabetes (23213_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cilia- and flagella-associated protein 300 in blood serum http://purl.obolibrary.org/obo/OBA_2044864 GCST90236260 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regucalcin level in Chronic kidney disease with hypertension and no diabetes (23224_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regucalcin in blood serum http://purl.obolibrary.org/obo/OBA_2043251 GCST90236261 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase TRIM62 level in Chronic kidney disease with hypertension and no diabetes (23225_26) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of E3 ubiquitin-protein ligase TRIM62 in blood serum http://purl.obolibrary.org/obo/OBA_2044530 GCST90236262 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C12orf76 level in Chronic kidney disease with hypertension and no diabetes (23228_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C12orf76 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044912 GCST90236263 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit Tim10 B level in Chronic kidney disease with hypertension and no diabetes (23241_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import inner membrane translocase subunit Tim9 B in blood serum http://purl.obolibrary.org/obo/OBA_2041636 GCST90236264 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sjoegren syndrome nuclear autoantigen 1 level in Chronic kidney disease with hypertension and no diabetes (23242_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule nucleation factor SSNA1 in blood serum http://purl.obolibrary.org/obo/OBA_2043664 GCST90236265 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S25 level in Chronic kidney disease with hypertension and no diabetes (23243_120) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 40S ribosomal protein S25 in blood serum http://purl.obolibrary.org/obo/OBA_2043334 GCST90236266 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Speriolin-like protein level in Chronic kidney disease with hypertension and no diabetes (23245_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of speriolin-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2044869 GCST90236267 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biogenesis of lysosome-related organelles complex 1 subunit 1 level in Chronic kidney disease with hypertension and no diabetes (23246_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of biogenesis of lysosome-related organelles complex 1 subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040805 GCST90236268 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. X antigen family member 2 level in Chronic kidney disease with hypertension and no diabetes (23248_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of X antigen family member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044147 GCST90236269 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein-like 4 level in Chronic kidney disease with hypertension and no diabetes (23250_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein-like 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043807 GCST90236270 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 3 level in Chronic kidney disease with hypertension and no diabetes (23252_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041402 GCST90236271 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catechol O-methyltransferase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (23253_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of catechol O-methyltransferase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041093 GCST90236272 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3 level in Chronic kidney disease with hypertension and no diabetes (23254_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044730 GCST90236273 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-33A level in Chronic kidney disease with hypertension and no diabetes (23255_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-33A in blood serum http://purl.obolibrary.org/obo/OBA_2043154 GCST90236274 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TLD domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (23256_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TLD domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044811 GCST90236275 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COMM domain-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (23257_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of COMM domain-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044273 GCST90236276 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable G-protein coupled receptor 101 level in Chronic kidney disease with hypertension and no diabetes (11670_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable G-protein coupled receptor 101 in blood serum http://purl.obolibrary.org/obo/OBA_2040306 GCST90233346 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peregrin level in Chronic kidney disease with hypertension and no diabetes (11671_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peregrin in blood serum http://purl.obolibrary.org/obo/OBA_2040829 GCST90233347 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly(ADP-ribose) glycohydrolase ARH3 level in Chronic kidney disease with hypertension and no diabetes (17332_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ADP-ribosylhydrolase ARH3 in blood serum http://purl.obolibrary.org/obo/OBA_2040525 GCST90234661 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Medium-chain specific acyl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17333_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of medium-chain specific acyl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040469 GCST90234662 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-responsive element-binding protein 3-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (17336_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-responsive element-binding protein 3-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041133 GCST90234663 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional repressor protein YY1 level in Chronic kidney disease with hypertension and no diabetes (17337_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional repressor protein YY1 in blood serum http://purl.obolibrary.org/obo/OBA_2044168 GCST90234664 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acetyl-CoA acetyltransferase, cytosolic level in Chronic kidney disease with hypertension and no diabetes (17341_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acetyl-CoA acetyltransferase, cytosolic in blood serum http://purl.obolibrary.org/obo/OBA_2040474 GCST90234665 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anterior gradient protein 3 level in Chronic kidney disease with hypertension and no diabetes (17342_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anterior gradient protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040537 GCST90234666 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaphilin level in Chronic kidney disease with hypertension and no diabetes (17343_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaphilin in blood serum http://purl.obolibrary.org/obo/OBA_2043570 GCST90234667 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stomatin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (17344_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stomatin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043706 GCST90234668 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin reductase 3 level in Chronic kidney disease with hypertension and no diabetes (17345_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostaglandin reductase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044540 GCST90234669 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follicular dendritic cell secreted peptide level in Chronic kidney disease with hypertension and no diabetes (17346_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of follicular dendritic cell secreted peptide in blood serum http://purl.obolibrary.org/obo/OBA_2041568 GCST90234670 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Axin interactor, dorsalization-associated protein level in Chronic kidney disease with hypertension and no diabetes (17347_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Axin interactor, dorsalization-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2040540 GCST90234671 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptojanin-2-binding protein level in Chronic kidney disease with hypertension and no diabetes (17348_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptojanin-2-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2043747 GCST90234672 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Charged multivesicular body protein 2b level in Chronic kidney disease with hypertension and no diabetes (17350_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of charged multivesicular body protein 2b in blood serum http://purl.obolibrary.org/obo/OBA_2041011 GCST90234673 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-4 level in Chronic kidney disease with hypertension and no diabetes (17355_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043754 GCST90234674 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 family member 10 level in Chronic kidney disease with hypertension and no diabetes (17356_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-1 family member 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042005 GCST90234675 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. O-phosphoseryl-tRNA(Sec) selenium transferase level in Chronic kidney disease with hypertension and no diabetes (17357_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of O-phosphoseryl-tRNA(Sec) selenium transferase in blood serum http://purl.obolibrary.org/obo/OBA_2043445 GCST90234676 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Von Hippel-Lindau disease tumor suppressor level in Chronic kidney disease with hypertension and no diabetes (17362_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of von Hippel-Lindau disease tumor suppressor in blood serum http://purl.obolibrary.org/obo/OBA_2044097 GCST90234677 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U2 small nuclear ribonucleoprotein B'' level in Chronic kidney disease with hypertension and no diabetes (17364_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U2 small nuclear ribonucleoprotein B'' in blood serum http://purl.obolibrary.org/obo/OBA_2043573 GCST90234678 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kynurenine--oxoglutarate transaminase 1 level in Chronic kidney disease with hypertension and no diabetes (17365_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kynurenine--oxoglutarate transaminase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040924 GCST90234679 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DCN1-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (17366_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DCN1-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041246 GCST90234680 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stathmin level in Chronic kidney disease with hypertension and no diabetes (17367_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stathmin in blood serum http://purl.obolibrary.org/obo/OBA_2043701 GCST90234681 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mycophenolic acid acyl-glucuronide esterase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17370_186) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of palmitoyl-protein thioesterase ABHD10, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044250 GCST90234682 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4E-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (17372_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of eukaryotic translation initiation factor 4E-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041454 GCST90234683 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ceruloplasmin level in Chronic kidney disease with hypertension and no diabetes (17453_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 GCST90234709 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor-like protein 6 level in Chronic kidney disease with hypertension and no diabetes (17454_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epidermal growth factor-like protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041425 GCST90234710 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Folate receptor alpha level in Chronic kidney disease with hypertension and no diabetes (17455_42) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of folate receptor alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041601 GCST90234711 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Golgi membrane protein 1 level in Chronic kidney disease with hypertension and no diabetes (17456_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Golgi membrane protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041762 GCST90234712 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon-induced GTP-binding protein Mx1 level in Chronic kidney disease with hypertension and no diabetes (17460_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon-induced GTP-binding protein Mx1 in blood serum http://purl.obolibrary.org/obo/OBA_2042469 GCST90234713 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 1 level in Chronic kidney disease with hypertension and no diabetes (17462_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon regulatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021908 GCST90234714 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-CoA synthetase family member 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17466_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of medium-chain acyl-CoA ligase ACSF2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040487 GCST90234715 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dehydrogenase/reductase SDR family member 9 level in Chronic kidney disease with hypertension and no diabetes (17467_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of dehydrogenase/reductase SDR family member 9 in blood serum http://purl.obolibrary.org/obo/OBA_2041297 GCST90234716 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Suppressor of fused homolog level in Chronic kidney disease with hypertension and no diabetes (17468_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of suppressor of fused homolog in blood serum http://purl.obolibrary.org/obo/OBA_2040435 GCST90234717 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. YEATS domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (17474_106) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of YEATS domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044161 GCST90234718 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphokine-activated killer T-cell-originated protein kinase level in Chronic kidney disease with hypertension and no diabetes (17475_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lymphokine-activated killer T-cell-originated protein kinase in blood serum http://purl.obolibrary.org/obo/OBA_2042773 GCST90234719 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD-dependent protein deacetylase sirtuin-3, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17495_141) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of NAD-dependent protein deacetylase sirtuin-3, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044358 GCST90234720 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylated-alpha-linked acidic dipeptidase-like protein level in Chronic kidney disease with hypertension and no diabetes (17505_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aminopeptidase NAALADL1 in blood serum http://purl.obolibrary.org/obo/OBA_2042496 GCST90234721 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 4-hydroxyphenylpyruvate dioxygenase level in Chronic kidney disease with hypertension and no diabetes (17509_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 4-hydroxyphenylpyruvate dioxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2041921 GCST90234722 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal recognition particle 14 kDa protein level in Chronic kidney disease with hypertension and no diabetes (17510_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of signal recognition particle 14 kDa protein in blood serum http://purl.obolibrary.org/obo/OBA_2043657 GCST90234723 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease P protein subunit p30 level in Chronic kidney disease with hypertension and no diabetes (17511_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonuclease P protein subunit p30 in blood serum http://purl.obolibrary.org/obo/OBA_2043327 GCST90234724 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-myc-interactor level in Chronic kidney disease with hypertension and no diabetes (17512_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of N-myc-interactor in blood serum http://purl.obolibrary.org/obo/OBA_2042598 GCST90234725 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A11 level in Chronic kidney disease with hypertension and no diabetes (17513_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A11 in blood serum http://purl.obolibrary.org/obo/OBA_2040598 GCST90234726 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-21 level in Chronic kidney disease with hypertension and no diabetes (17514_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-21 in blood serum http://purl.obolibrary.org/obo/OBA_2043144 GCST90234727 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 13 level in Chronic kidney disease with hypertension and no diabetes (17515_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock 70 kDa protein 13 in blood serum http://purl.obolibrary.org/obo/OBA_2041946 GCST90234728 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-3A level in Chronic kidney disease with hypertension and no diabetes (17516_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-3A in blood serum http://purl.obolibrary.org/obo/OBA_2043158 GCST90234729 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibitor of growth protein 4 level in Chronic kidney disease with hypertension and no diabetes (17671_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of inhibitor of growth protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042027 GCST90234730 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastric intrinsic factor level in Chronic kidney disease with hypertension and no diabetes (17672_184) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cobalamin binding intrinsic factor in blood serum http://purl.obolibrary.org/obo/OBA_2041717 GCST90234731 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 5B, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17673_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbonic anhydrase 5B, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040860 GCST90234732 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-coenzyme A thioesterase 13 level in Chronic kidney disease with hypertension and no diabetes (17675_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-coenzyme A thioesterase 13 in blood serum http://purl.obolibrary.org/obo/OBA_2044251 GCST90234733 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldo-keto reductase family 1 member C3 level in Chronic kidney disease with hypertension and no diabetes (17377_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member C3 in blood serum http://purl.obolibrary.org/obo/OBA_2040551 GCST90234684 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 K level in Chronic kidney disease with hypertension and no diabetes (17380_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 K in blood serum http://purl.obolibrary.org/obo/OBA_2043998 GCST90234685 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. StAR-related lipid transfer protein 5 level in Chronic kidney disease with hypertension and no diabetes (17383_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of StAR-related lipid transfer protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043693 GCST90234686 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent 6-phosphofructokinase, muscle type level in Chronic kidney disease with hypertension and no diabetes (17384_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent 6-phosphofructokinase, muscle type in blood serum http://purl.obolibrary.org/obo/OBA_2042854 GCST90234687 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NF-kappa-B inhibitor beta level in Chronic kidney disease with hypertension and no diabetes (17387_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NF-kappa-B inhibitor beta in blood serum http://purl.obolibrary.org/obo/OBA_2040433 GCST90234688 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Splicing factor 45 level in Chronic kidney disease with hypertension and no diabetes (17391_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of splicing factor 45 in blood serum http://purl.obolibrary.org/obo/OBA_2043204 GCST90234689 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Short-chain specific acyl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17393_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of short-chain specific acyl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040470 GCST90234690 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase 1A level in Chronic kidney disease with hypertension and no diabetes (17396_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alcohol dehydrogenase 1A in blood serum http://purl.obolibrary.org/obo/OBA_2040513 GCST90234691 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Estradiol 17-beta-dehydrogenase 11 level in Chronic kidney disease with hypertension and no diabetes (17397_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of estradiol 17-beta-dehydrogenase 11 in blood serum http://purl.obolibrary.org/obo/OBA_2041939 GCST90234692 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heme oxygenase 1 level in Chronic kidney disease with hypertension and no diabetes (17398_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heme oxygenase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041895 GCST90234693 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-coenzyme A thioesterase 8 level in Chronic kidney disease with hypertension and no diabetes (17400_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-coenzyme A thioesterase 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040481 GCST90234694 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Short/branched chain specific acyl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17403_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of short/branched chain specific acyl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040471 GCST90234695 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 5B level in Chronic kidney disease with hypertension and no diabetes (17404_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ADP-ribosylation factor-like protein 5B in blood serum http://purl.obolibrary.org/obo/OBA_2040671 GCST90234696 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase isozyme L5 level in Chronic kidney disease with hypertension and no diabetes (17405_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase isozyme L5 in blood serum http://purl.obolibrary.org/obo/OBA_2044016 GCST90234697 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centrin-3 level in Chronic kidney disease with hypertension and no diabetes (17410_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centrin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040992 GCST90234698 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin recognition factor in ER-associated degradation protein 1 level in Chronic kidney disease with hypertension and no diabetes (17411_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin recognition factor in ER-associated degradation protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044020 GCST90234699 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testin level in Chronic kidney disease with hypertension and no diabetes (17419_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of testin in blood serum http://purl.obolibrary.org/obo/OBA_2043828 GCST90234700 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-3 level in Chronic kidney disease with hypertension and no diabetes (17427_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroligin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042589 GCST90234701 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenylate kinase 4, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17432_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adenylate kinase 4, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044241 GCST90234702 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Electron transfer flavoprotein subunit alpha, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17435_43) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of electron transfer flavoprotein subunit alpha, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041514 GCST90234703 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase I isoform gamma-2 level in Chronic kidney disease with hypertension and no diabetes (17436_193) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of casein kinase I isoform gamma-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041172 GCST90234704 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intestinal-type alkaline phosphatase level in Chronic kidney disease with hypertension and no diabetes (17441_4) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of intestinal alkaline phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2040574 GCST90234705 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted frizzled-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (17447_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secreted frizzled-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043476 GCST90234706 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD9 antigen level in Chronic kidney disease with hypertension and no diabetes (17449_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD9 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040948 GCST90234707 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histidine--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (17450_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histidyl-tRNA synthetase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2041838 GCST90234708 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexophilin-1 level in Chronic kidney disease with hypertension and no diabetes (23002_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurexophilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008244 GCST90236227 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 5-phosphate 4-kinase type-2 beta level in Chronic kidney disease with hypertension and no diabetes (23006_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol 5-phosphate 4-kinase type-2 beta in blood serum http://purl.obolibrary.org/obo/OBA_2042898 GCST90236228 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junction plakoglobin level in Chronic kidney disease with hypertension and no diabetes (23007_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of junction plakoglobin in blood serum http://purl.obolibrary.org/obo/OBA_2042079 GCST90236229 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-2A level in Chronic kidney disease with hypertension and no diabetes (23008_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-2A in blood serum http://purl.obolibrary.org/obo/OBA_2043151 GCST90236230 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Reticulocalbin-3 level in Chronic kidney disease with hypertension and no diabetes (23017_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of reticulocalbin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043220 GCST90236231 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lithostathine-1-beta level in Chronic kidney disease with hypertension and no diabetes (23018_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lithostathine-1-beta in blood serum http://purl.obolibrary.org/obo/OBA_2043231 GCST90236232 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 4 level in Chronic kidney disease with hypertension and no diabetes (23020_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043261 GCST90236233 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab GDP dissociation inhibitor alpha level in Chronic kidney disease with hypertension and no diabetes (23022_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab GDP dissociation inhibitor alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041699 GCST90236234 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A14 level in Chronic kidney disease with hypertension and no diabetes (23023_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A14 in blood serum http://purl.obolibrary.org/obo/OBA_2043365 GCST90236235 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein SAR1a level in Chronic kidney disease with hypertension and no diabetes (23024_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein SAR1a in blood serum http://purl.obolibrary.org/obo/OBA_2043380 GCST90236236 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntenin-2 level in Chronic kidney disease with hypertension and no diabetes (23028_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntenin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043412 GCST90236237 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endophilin-A3 level in Chronic kidney disease with hypertension and no diabetes (23029_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of endophilin-A3 in blood serum http://purl.obolibrary.org/obo/OBA_2043492 GCST90236238 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 5 level in Chronic kidney disease with hypertension and no diabetes (23030_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sialic acid-binding Ig-like lectin 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040358 GCST90236239 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD-dependent protein deacetylase sirtuin-2 level in Chronic kidney disease with hypertension and no diabetes (23031_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 NAD-dependent protein deacetylase sirtuin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008241 GCST90236240 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. VPS10 domain-containing receptor SorCS3 level in Chronic kidney disease with hypertension and no diabetes (23034_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of VPS10 domain-containing receptor SorCS3 in blood serum http://purl.obolibrary.org/obo/OBA_2044491 GCST90236241 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 D3 level in Chronic kidney disease with hypertension and no diabetes (23037_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 D3 in blood serum http://purl.obolibrary.org/obo/OBA_2040419 GCST90236242 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5B level in Chronic kidney disease with hypertension and no diabetes (23038_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of netrin receptor UNC5B in blood serum http://purl.obolibrary.org/obo/OBA_2044038 GCST90236243 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein MOX-2 level in Chronic kidney disease with hypertension and no diabetes (23039_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein MOX-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042338 GCST90236244 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelial cell-derived lipase level in Chronic kidney disease with hypertension and no diabetes (23148_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endothelial lipase in blood serum http://purl.obolibrary.org/obo/OBA_2042207 GCST90236245 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 level in Chronic kidney disease with hypertension and no diabetes (23152_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043887 GCST90236246 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD6 level in Chronic kidney disease with hypertension and no diabetes (23161_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of BTB/POZ domain-containing protein KCTD6 in blood serum http://purl.obolibrary.org/obo/OBA_2044320 GCST90236247 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase kinase kinase 10 level in Chronic kidney disease with hypertension and no diabetes (23162_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase kinase kinase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042286 GCST90236248 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial pyruvate carrier 1 level in Chronic kidney disease with hypertension and no diabetes (23164_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of brain protein 44-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2040828 GCST90236249 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metalloproteinase inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (23173_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 metalloproteinase inhibitor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020566 GCST90236250 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-dystroglycan level in Chronic kidney disease with hypertension and no diabetes (23176_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dystroglycan 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041225 GCST90236251 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock factor protein 1 level in Chronic kidney disease with hypertension and no diabetes (11616_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock protein beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0010595 GCST90233321 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-L level in Chronic kidney disease with hypertension and no diabetes (11617_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin alpha-L in blood serum http://purl.obolibrary.org/obo/OBA_2040227 GCST90233322 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional activator Myb level in Chronic kidney disease with hypertension and no diabetes (11618_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myb proto-oncogene protein in blood serum http://purl.obolibrary.org/obo/OBA_2042472 GCST90233323 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 variant 1 level in Chronic kidney disease with hypertension and no diabetes (11626_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 variant 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040431 GCST90233324 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TNF receptor-associated factor 4 level in Chronic kidney disease with hypertension and no diabetes (11629_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TNF receptor-associated factor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040406 GCST90233325 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activator of 90 kDa heat shock protein ATPase homolog 1 level in Chronic kidney disease with hypertension and no diabetes (11633_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activator of 90 kDa heat shock protein ATPase homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040539 GCST90233326 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 10 level in Chronic kidney disease with hypertension and no diabetes (11634_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043253 GCST90233327 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transgelin-2 level in Chronic kidney disease with hypertension and no diabetes (11636_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 transgelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021884 GCST90233328 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-galactosyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (11638_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-galactosyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040746 GCST90233329 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase DTX3L level in Chronic kidney disease with hypertension and no diabetes (11643_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase DTX3L in blood serum http://purl.obolibrary.org/obo/OBA_2041376 GCST90233330 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolyl 4-hydroxylase subunit alpha-1 level in Chronic kidney disease with hypertension and no diabetes (11645_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prolyl 4-hydroxylase subunit alpha-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042731 GCST90233331 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 9 level in Chronic kidney disease with hypertension and no diabetes (11646_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 9 in blood serum http://purl.obolibrary.org/obo/OBA_2041027 GCST90233332 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-10 level in Chronic kidney disease with hypertension and no diabetes (11647_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233333 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal membrane-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (11649_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stromal membrane-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043552 GCST90233334 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein argonaute-1 level in Chronic kidney disease with hypertension and no diabetes (11651_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein argonaute-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041441 GCST90233335 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium- and chloride-dependent glycine transporter 1 level in Chronic kidney disease with hypertension and no diabetes (11653_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium- and chloride-dependent glycine transporter 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043542 GCST90233336 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurensin-1 level in Chronic kidney disease with hypertension and no diabetes (11654_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurensin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042643 GCST90233337 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ena/VASP-like protein level in Chronic kidney disease with hypertension and no diabetes (11656_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ena/VASP-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2041521 GCST90233338 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Suppressor of cytokine signaling 7 level in Chronic kidney disease with hypertension and no diabetes (11657_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of suppressor of cytokine signaling 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043593 GCST90233339 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Clathrin interactor 1 level in Chronic kidney disease with hypertension and no diabetes (11659_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of clathrin interactor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041052 GCST90233340 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NACHT, LRR and PYD domains-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (11661_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NACHT, LRR and PYD domains-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042591 GCST90233341 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor GTPase-activating protein 2 level in Chronic kidney disease with hypertension and no diabetes (11664_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor GTPase-activating protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040645 GCST90233342 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 8 level in Chronic kidney disease with hypertension and no diabetes (11666_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 8 in blood serum http://purl.obolibrary.org/obo/OBA_2043263 GCST90233343 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tensin-2 level in Chronic kidney disease with hypertension and no diabetes (11667_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tensin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043826 GCST90233344 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Solute carrier organic anion transporter family member 5A1 level in Chronic kidney disease with hypertension and no diabetes (11669_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of solute carrier organic anion transporter family member 5A1 in blood serum http://purl.obolibrary.org/obo/OBA_2044227 GCST90233345 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cdc42-interacting protein 4 level in Chronic kidney disease with hypertension and no diabetes (17676_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Cdc42-interacting protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043940 GCST90234734 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and immunoglobulin domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (17678_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-set and immunoglobulin domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044115 GCST90234735 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-B receptor 1 level in Chronic kidney disease with hypertension and no diabetes (17680_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ephrin type-B receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041493 GCST90234736 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane cofactor protein level in Chronic kidney disease with hypertension and no diabetes (17682_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane cofactor protein in blood serum http://purl.obolibrary.org/obo/OBA_2040295 GCST90234737 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COMM domain-containing protein 9 level in Chronic kidney disease with hypertension and no diabetes (17683_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of COMM domain-containing protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2044272 GCST90234738 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein A-IV level in Chronic kidney disease with hypertension and no diabetes (17685_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 apolipoprotein A-IV measurement http://www.ebi.ac.uk/efo/EFO_0007848 GCST90234739 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin-folding cofactor B level in Chronic kidney disease with hypertension and no diabetes (17686_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin-folding cofactor B in blood serum http://purl.obolibrary.org/obo/OBA_2043790 GCST90234740 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tripeptidyl-peptidase 1 level in Chronic kidney disease with hypertension and no diabetes (17691_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tripeptidyl-peptidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043913 GCST90234741 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin subfamily 3 member A3 level in Chronic kidney disease with hypertension and no diabetes (17692_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of butyrophilin subfamily 3 member A3 in blood serum http://purl.obolibrary.org/obo/OBA_2044724 GCST90234742 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Septin-6 level in Chronic kidney disease with hypertension and no diabetes (17693_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of septin-6 in blood serum http://purl.obolibrary.org/obo/OBA_2043451 GCST90234743 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome activator complex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (17694_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome activator complex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043079 GCST90234744 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TIR domain-containing adapter molecule 2 level in Chronic kidney disease with hypertension and no diabetes (17696_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TIR domain-containing adapter molecule 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040320 GCST90234745 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Esterase OVCA2 level in Chronic kidney disease with hypertension and no diabetes (17697_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of esterase OVCA2 in blood serum http://purl.obolibrary.org/obo/OBA_2042725 GCST90234746 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WW domain-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (17698_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WW domain-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044379 GCST90234747 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein timeless homolog level in Chronic kidney disease with hypertension and no diabetes (17699_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein timeless in blood serum http://purl.obolibrary.org/obo/OBA_2043851 GCST90234748 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-glucuronosyltransferase 1-1 level in Chronic kidney disease with hypertension and no diabetes (17702_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UDP-glucuronosyltransferase 1A1 in blood serum http://purl.obolibrary.org/obo/OBA_2044023 GCST90234749 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Geminin level in Chronic kidney disease with hypertension and no diabetes (17703_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of geminin in blood serum http://purl.obolibrary.org/obo/OBA_2041744 GCST90234750 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock protein 105 kDa level in Chronic kidney disease with hypertension and no diabetes (17704_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock protein 105 kDa in blood serum http://purl.obolibrary.org/obo/OBA_2040442 GCST90234751 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1-syntrophin level in Chronic kidney disease with hypertension and no diabetes (22946_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1-syntrophin in blood serum http://purl.obolibrary.org/obo/OBA_2043579 GCST90236195 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 3 level in Chronic kidney disease with hypertension and no diabetes (22948_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone morphogenetic protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040813 GCST90236196 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin subfamily 3 member A3 level in Chronic kidney disease with hypertension and no diabetes (22950_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of butyrophilin subfamily 3 member A3 in blood serum http://purl.obolibrary.org/obo/OBA_2044724 GCST90236197 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 2-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (22952_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 2-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040967 GCST90236198 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CCAAT/enhancer-binding protein beta level in Chronic kidney disease with hypertension and no diabetes (22953_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 CCAAT/enhancer-binding protein beta measurement http://www.ebi.ac.uk/efo/EFO_0021905 GCST90236199 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chloride intracellular channel protein 2 level in Chronic kidney disease with hypertension and no diabetes (22954_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chloride intracellular channel protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041048 GCST90236200 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (22955_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinol-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043211 GCST90236201 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Destrin level in Chronic kidney disease with hypertension and no diabetes (22958_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of destrin in blood serum http://purl.obolibrary.org/obo/OBA_2041371 GCST90236202 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dickkopf-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (22959_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 Dickkopf-related protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0008110 GCST90236203 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low affinity immunoglobulin gamma Fc region receptor II-b level in Chronic kidney disease with hypertension and no diabetes (22960_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 low affinity immunoglobulin gamma Fc region receptor II-b measurement http://www.ebi.ac.uk/efo/EFO_0021970 GCST90236204 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ficolin-1 level in Chronic kidney disease with hypertension and no diabetes (22961_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 ficolin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008134 GCST90236205 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-associated membrane protein 2 level in Chronic kidney disease with hypertension and no diabetes (22963_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-associated membrane protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044076 GCST90236206 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-aminobutyric acid receptor-associated protein level in Chronic kidney disease with hypertension and no diabetes (22966_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-aminobutyric acid receptor-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2041647 GCST90236207 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 7 level in Chronic kidney disease with hypertension and no diabetes (22967_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth/differentiation factor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040212 GCST90236208 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G antigen 2D level in Chronic kidney disease with hypertension and no diabetes (22968_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of G antigen 2D in blood serum http://purl.obolibrary.org/obo/OBA_2041654 GCST90236209 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 7 level in Chronic kidney disease with hypertension and no diabetes (22969_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 7 measurement http://www.ebi.ac.uk/efo/EFO_0008054 GCST90236210 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ domain-containing protein GIPC1 level in Chronic kidney disease with hypertension and no diabetes (22970_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ domain-containing protein GIPC1 in blood serum http://purl.obolibrary.org/obo/OBA_2041721 GCST90236211 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gro-beta level in Chronic kidney disease with hypertension and no diabetes (22972_26) 466 African American individuals NA Illumina [14870897] (imputed) 3 level of C-X-C motif chemokine 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041207 GCST90236212 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gro-gamma level in Chronic kidney disease with hypertension and no diabetes (22973_8) 466 African American individuals NA Illumina [14870897] (imputed) 8 level of C-X-C motif chemokine 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041208 GCST90236213 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H2B type 2-E level in Chronic kidney disease with hypertension and no diabetes (22974_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 histone H2B type 2-E measurement http://www.ebi.ac.uk/efo/EFO_0021952 GCST90236214 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein HEXIM1 level in Chronic kidney disease with hypertension and no diabetes (22977_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein HEXIM1 in blood serum http://purl.obolibrary.org/obo/OBA_2041866 GCST90236215 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High mobility group protein B2 level in Chronic kidney disease with hypertension and no diabetes (22978_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high mobility group protein B2 in blood serum http://purl.obolibrary.org/obo/OBA_2041889 GCST90236216 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hippocalcin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (22981_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hippocalcin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041920 GCST90236217 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic initiation factor 4A-II level in Chronic kidney disease with hypertension and no diabetes (22984_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic initiation factor 4A-II in blood serum http://purl.obolibrary.org/obo/OBA_2041450 GCST90236218 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (22985_160) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90236219 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 9 level in Chronic kidney disease with hypertension and no diabetes (22987_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020581 GCST90236220 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein lin-7 homolog A level in Chronic kidney disease with hypertension and no diabetes (22989_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein lin-7 homolog A in blood serum http://purl.obolibrary.org/obo/OBA_2042205 GCST90236221 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein lin-7 homolog B level in Chronic kidney disease with hypertension and no diabetes (22990_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein lin-7 homolog B measurement http://www.ebi.ac.uk/efo/EFO_0021978 GCST90236222 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 6 level in Chronic kidney disease with hypertension and no diabetes (22991_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042268 GCST90236223 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated protein RP/EB family member 3 level in Chronic kidney disease with hypertension and no diabetes (22992_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated protein RP/EB family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042298 GCST90236224 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 22 level in Chronic kidney disease with hypertension and no diabetes (22993_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 22 measurement http://www.ebi.ac.uk/efo/EFO_0020196 GCST90236225 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-1 level in Chronic kidney disease with hypertension and no diabetes (23000_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroligin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042588 GCST90236226 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase assembly factor 7 level in Chronic kidney disease with hypertension and no diabetes (23258_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome c oxidase assembly factor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044676 GCST90236277 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EEF1A lysine methyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (23259_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EEF1A lysine methyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042494 GCST90236278 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C1orf50 level in Chronic kidney disease with hypertension and no diabetes (23261_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C1orf50 in blood serum http://purl.obolibrary.org/obo/OBA_2044866 GCST90236279 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-crystallin B3 level in Chronic kidney disease with hypertension and no diabetes (23262_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-crystallin B3 in blood serum http://purl.obolibrary.org/obo/OBA_2041157 GCST90236280 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD15 level in Chronic kidney disease with hypertension and no diabetes (23263_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD15 in blood serum http://purl.obolibrary.org/obo/OBA_2044316 GCST90236281 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mediator of RNA polymerase II transcription subunit 10 level in Chronic kidney disease with hypertension and no diabetes (23264_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mediator of RNA polymerase II transcription subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042325 GCST90236282 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor protein D54 level in Chronic kidney disease with hypertension and no diabetes (23265_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor protein D54 in blood serum http://purl.obolibrary.org/obo/OBA_2043908 GCST90236283 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MIT domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (23266_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MIT domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042371 GCST90236284 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD6 level in Chronic kidney disease with hypertension and no diabetes (23267_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD6 in blood serum http://purl.obolibrary.org/obo/OBA_2044320 GCST90236285 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FRG1 level in Chronic kidney disease with hypertension and no diabetes (23268_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FRG1 in blood serum http://purl.obolibrary.org/obo/OBA_2041617 GCST90236286 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CKLF-like MARVEL transmembrane domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (23269_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CKLF-like MARVEL transmembrane domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044716 GCST90236287 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermatogenesis-associated protein 33 level in Chronic kidney disease with hypertension and no diabetes (23270_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spermatogenesis-associated protein 33 in blood serum http://purl.obolibrary.org/obo/OBA_2044810 GCST90236288 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein DPCD level in Chronic kidney disease with hypertension and no diabetes (23272_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein DPCD in blood serum http://purl.obolibrary.org/obo/OBA_2041347 GCST90236289 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerase III subunit RPC9 level in Chronic kidney disease with hypertension and no diabetes (17771_35) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of DNA-directed RNA polymerase III subunit RPC9 in blood serum http://purl.obolibrary.org/obo/OBA_2041130 GCST90234787 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin D level in Chronic kidney disease with hypertension and no diabetes (17772_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin D in blood serum http://purl.obolibrary.org/obo/OBA_2043988 GCST90234788 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-soluble NSF attachment protein level in Chronic kidney disease with hypertension and no diabetes (17773_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-soluble NSF attachment protein in blood serum http://purl.obolibrary.org/obo/OBA_2042511 GCST90234789 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small nuclear ribonucleoprotein Sm D3 level in Chronic kidney disease with hypertension and no diabetes (17774_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small nuclear ribonucleoprotein Sm D3 in blood serum http://purl.obolibrary.org/obo/OBA_2043576 GCST90234790 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transgelin-3 level in Chronic kidney disease with hypertension and no diabetes (17775_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transgelin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043773 GCST90234791 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal trans-2-enoyl-CoA reductase level in Chronic kidney disease with hypertension and no diabetes (17776_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisomal trans-2-enoyl-CoA reductase in blood serum http://purl.obolibrary.org/obo/OBA_2042842 GCST90234792 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine dehydratase-like level in Chronic kidney disease with hypertension and no diabetes (17777_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine dehydratase-like in blood serum http://purl.obolibrary.org/obo/OBA_2043416 GCST90234793 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated proteins 1A/1B light chain 3A level in Chronic kidney disease with hypertension and no diabetes (17781_191) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated proteins 1A/1B light chain 3A in blood serum http://purl.obolibrary.org/obo/OBA_2042282 GCST90234794 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-ketoacyl-CoA thiolase, peroxisomal level in Chronic kidney disease with hypertension and no diabetes (17782_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 3-ketoacyl-CoA thiolase, peroxisomal in blood serum http://purl.obolibrary.org/obo/OBA_2040466 GCST90234795 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17783_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of corrinoid adenosyltransferase MMAB in blood serum http://purl.obolibrary.org/obo/OBA_2042383 GCST90234796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2'-deoxynucleoside 5'-phosphate N-hydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (17785_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 2'-deoxynucleoside 5'-phosphate N-hydrolase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043219 GCST90234797 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Geranylgeranyl pyrophosphate synthase level in Chronic kidney disease with hypertension and no diabetes (17786_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of geranylgeranyl pyrophosphate synthase in blood serum http://purl.obolibrary.org/obo/OBA_2041711 GCST90234798 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Enoyl-CoA hydratase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17787_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of enoyl-CoA hydratase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041407 GCST90234799 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nicotinate-nucleotide pyrophosphorylase [carboxylating] level in Chronic kidney disease with hypertension and no diabetes (17789_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nicotinate-nucleotide pyrophosphorylase [carboxylating] in blood serum http://purl.obolibrary.org/obo/OBA_2043133 GCST90234800 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hippocalcin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (17791_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hippocalcin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041920 GCST90234801 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Succinate-semialdehyde dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17792_158) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of succinate-semialdehyde dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040564 GCST90234802 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein Di-Ras1 level in Chronic kidney disease with hypertension and no diabetes (17793_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein Di-Ras1 in blood serum http://purl.obolibrary.org/obo/OBA_2041303 GCST90234803 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphomannomutase 2 level in Chronic kidney disease with hypertension and no diabetes (17794_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphomannomutase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042943 GCST90234804 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U6 snRNA-associated Sm-like protein LSm1 level in Chronic kidney disease with hypertension and no diabetes (17795_176) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U6 snRNA-associated Sm-like protein LSm1 in blood serum http://purl.obolibrary.org/obo/OBA_2042240 GCST90234805 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol monophosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (17796_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of inositol monophosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042021 GCST90234806 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cullin-1 level in Chronic kidney disease with hypertension and no diabetes (17797_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fungal/metazoan cullin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040193 GCST90234807 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 6-phosphogluconolactonase level in Chronic kidney disease with hypertension and no diabetes (17799_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 6-phosphogluconolactonase in blood serum http://purl.obolibrary.org/obo/OBA_2042861 GCST90234808 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SCAN domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (17800_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SCAN domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043391 GCST90234809 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid synthase level in Chronic kidney disease with hypertension and no diabetes (17802_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sialic acid synthase in blood serum http://purl.obolibrary.org/obo/OBA_2042505 GCST90234810 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyridoxine-5'-phosphate oxidase level in Chronic kidney disease with hypertension and no diabetes (17804_102) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pyridoxine-5'-phosphate oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2042955 GCST90234811 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (23361_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043207 GCST90236355 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibronectin type III domain-containing protein 8 level in Chronic kidney disease with hypertension and no diabetes (23365_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibronectin type III domain-containing protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044543 GCST90236356 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like protein 7 level in Chronic kidney disease with hypertension and no diabetes (23366_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044010 GCST90236357 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 40 level in Chronic kidney disease with hypertension and no diabetes (23367_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 40 in blood serum http://purl.obolibrary.org/obo/OBA_2044520 GCST90236358 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phytanoyl-CoA dioxygenase, peroxisomal level in Chronic kidney disease with hypertension and no diabetes (23369_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phytanoyl-CoA dioxygenase, peroxisomal in blood serum http://purl.obolibrary.org/obo/OBA_2042880 GCST90236359 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Voltage-gated potassium channel subunit beta-3 level in Chronic kidney disease with hypertension and no diabetes (23370_39) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of voltage-gated potassium channel subunit beta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042087 GCST90236360 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NIF3-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (23371_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NIF3-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042581 GCST90236361 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diphthine methyl ester synthase level in Chronic kidney disease with hypertension and no diabetes (23373_77) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of diphthine methyl ester synthase in blood serum http://purl.obolibrary.org/obo/OBA_2041351 GCST90236362 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-terminal EF-hand calcium-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (23374_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-terminal EF-hand calcium-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042549 GCST90236363 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ret finger protein-like 3 level in Chronic kidney disease with hypertension and no diabetes (23375_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ret finger protein-like 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043248 GCST90236364 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Actin-related protein 2/3 complex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (23376_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin-related protein 2/3 complex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040681 GCST90236365 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CGG triplet repeat-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (23378_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CGG triplet repeat-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040996 GCST90236366 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0472 protein C16orf72 level in Chronic kidney disease with hypertension and no diabetes (23379_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of HUWE1-associated protein modifying stress responses in blood serum http://purl.obolibrary.org/obo/OBA_2044826 GCST90236367 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trans-3-hydroxy-L-proline dehydratase level in Chronic kidney disease with hypertension and no diabetes (23380_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trans-3-hydroxy-L-proline dehydratase in blood serum http://purl.obolibrary.org/obo/OBA_2044572 GCST90236368 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Septin-1 level in Chronic kidney disease with hypertension and no diabetes (23381_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of septin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043446 GCST90236369 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Variable charge X-linked protein 3 level in Chronic kidney disease with hypertension and no diabetes (23382_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of variable charge X-linked protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044093 GCST90236370 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD17 level in Chronic kidney disease with hypertension and no diabetes (23384_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD17 in blood serum http://purl.obolibrary.org/obo/OBA_2044772 GCST90236371 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic arginine sensor for mTORC1 subunit 1 level in Chronic kidney disease with hypertension and no diabetes (23385_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosolic arginine sensor for mTORC1 subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041677 GCST90236372 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-complex protein 10A homolog 2 level in Chronic kidney disease with hypertension and no diabetes (23386_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90236373 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TIP41-like protein level in Chronic kidney disease with hypertension and no diabetes (23387_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TIP41-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2043860 GCST90236374 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fumarylacetoacetate hydrolase domain-containing protein 2A level in Chronic kidney disease with hypertension and no diabetes (23389_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fumarylacetoacetate hydrolase domain-containing protein 2A in blood serum http://purl.obolibrary.org/obo/OBA_2041544 GCST90236375 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family A member 3 level in Chronic kidney disease with hypertension and no diabetes (23392_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family A member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042927 GCST90236376 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 1-acylglycerol-3-phosphate O-acyltransferase ABHD5 level in Chronic kidney disease with hypertension and no diabetes (23393_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 1-acylglycerol-3-phosphate O-acyltransferase ABHD5 in blood serum http://purl.obolibrary.org/obo/OBA_2044689 GCST90236377 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth arrest-specific protein 2 level in Chronic kidney disease with hypertension and no diabetes (23394_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth arrest-specific protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041673 GCST90236378 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. KH domain-containing, RNA-binding, signal transduction-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (23395_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of KH domain-containing, RNA-binding, signal transduction-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042093 GCST90236379 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Survival motor neuron protein level in Chronic kidney disease with hypertension and no diabetes (23290_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of survival motor neuron protein in blood serum http://purl.obolibrary.org/obo/OBA_2044232 GCST90236305 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PTB-containing, cubilin and LRP1-interacting protein level in Chronic kidney disease with hypertension and no diabetes (23291_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PTB-containing, cubilin and LRP1-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2042886 GCST90236306 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centrosomal protein of 112 kDa level in Chronic kidney disease with hypertension and no diabetes (23292_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centrosomal protein of 112 kDa in blood serum http://purl.obolibrary.org/obo/OBA_2044525 GCST90236307 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione-specific gamma-glutamylcyclotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (23293_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione-specific gamma-glutamylcyclotransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040998 GCST90236308 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Max-like protein X level in Chronic kidney disease with hypertension and no diabetes (23294_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Max-like protein X in blood serum http://purl.obolibrary.org/obo/OBA_2042381 GCST90236309 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SARP-3 level in Chronic kidney disease with hypertension and no diabetes (23296_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secreted frizzled-related protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043477 GCST90236310 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-coenzyme A thioesterase THEM4 level in Chronic kidney disease with hypertension and no diabetes (23298_148) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-coenzyme A thioesterase THEM4 in blood serum http://purl.obolibrary.org/obo/OBA_2043841 GCST90236311 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin polymerization-promoting protein level in Chronic kidney disease with hypertension and no diabetes (23299_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin polymerization-promoting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043915 GCST90236312 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein with multiple splicing 2 level in Chronic kidney disease with hypertension and no diabetes (23300_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein with multiple splicing 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043215 GCST90236313 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MSX-2 level in Chronic kidney disease with hypertension and no diabetes (23301_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein MSX-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042445 GCST90236314 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proline-rich AKT1 substrate 1 level in Chronic kidney disease with hypertension and no diabetes (23302_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proline-rich AKT1 substrate 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040555 GCST90236315 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor expression-enhancing protein 2 level in Chronic kidney disease with hypertension and no diabetes (23305_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor expression-enhancing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043229 GCST90236316 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyamine-modulated factor 1 level in Chronic kidney disease with hypertension and no diabetes (23306_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyamine-modulated factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042942 GCST90236317 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Clusterin-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (23307_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of clusterin-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041060 GCST90236318 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD1 level in Chronic kidney disease with hypertension and no diabetes (23308_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044670 GCST90236319 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homologous-pairing protein 2 homolog level in Chronic kidney disease with hypertension and no diabetes (23309_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homologous-pairing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043075 GCST90236320 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal cell-derived factor 1 level in Chronic kidney disease with hypertension and no diabetes (2330_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 stromal cell-derived factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020756 GCST90236321 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-38 level in Chronic kidney disease with hypertension and no diabetes (23310_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-38 in blood serum http://purl.obolibrary.org/obo/OBA_2043156 GCST90236322 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease P protein subunit p25 level in Chronic kidney disease with hypertension and no diabetes (23311_19) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ribonuclease P protein subunit p25 in blood serum http://purl.obolibrary.org/obo/OBA_2043326 GCST90236323 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (23312_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043176 GCST90236324 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 103 level in Chronic kidney disease with hypertension and no diabetes (23314_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 103 in blood serum http://purl.obolibrary.org/obo/OBA_2044707 GCST90236325 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM9B level in Chronic kidney disease with hypertension and no diabetes (23315_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM9B in blood serum http://purl.obolibrary.org/obo/OBA_2044725 GCST90236326 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dehydrogenase/reductase SDR family member 11 level in Chronic kidney disease with hypertension and no diabetes (23317_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dehydrogenase/reductase SDR family member 11 in blood serum http://purl.obolibrary.org/obo/OBA_2044669 GCST90236327 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylcholine transfer protein level in Chronic kidney disease with hypertension and no diabetes (23318_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylcholine transfer protein in blood serum http://purl.obolibrary.org/obo/OBA_2042809 GCST90236328 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AN1-type zinc finger protein 2B level in Chronic kidney disease with hypertension and no diabetes (23319_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of AN1-type zinc finger protein 2B in blood serum http://purl.obolibrary.org/obo/OBA_2044178 GCST90236329 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Survival of motor neuron-related-splicing factor 30 level in Chronic kidney disease with hypertension and no diabetes (17805_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of survival of motor neuron-related-splicing factor 30 in blood serum http://purl.obolibrary.org/obo/OBA_2043556 GCST90234812 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntenin-1 level in Chronic kidney disease with hypertension and no diabetes (17806_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntenin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043411 GCST90234813 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Omega-amidase NIT2 level in Chronic kidney disease with hypertension and no diabetes (17808_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of omega-amidase NIT2 in blood serum http://purl.obolibrary.org/obo/OBA_2042584 GCST90234814 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfotransferase 1C2 level in Chronic kidney disease with hypertension and no diabetes (17811_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 1C2 in blood serum http://purl.obolibrary.org/obo/OBA_2043727 GCST90234815 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein tyrosine phosphatase type IVA 1 level in Chronic kidney disease with hypertension and no diabetes (17812_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein tyrosine phosphatase type IVA 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043097 GCST90234816 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Valacyclovir hydrolase level in Chronic kidney disease with hypertension and no diabetes (17813_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of valacyclovir hydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2040820 GCST90234817 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3'(2'),5'-bisphosphate nucleotidase 1 level in Chronic kidney disease with hypertension and no diabetes (17814_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 3'(2'),5'-bisphosphate nucleotidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040821 GCST90234818 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurocalcin-delta level in Chronic kidney disease with hypertension and no diabetes (17816_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurocalcin-delta in blood serum http://purl.obolibrary.org/obo/OBA_2042520 GCST90234819 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA damage-inducible transcript 4 protein level in Chronic kidney disease with hypertension and no diabetes (17817_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA damage-inducible transcript 4 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041255 GCST90234820 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein SGT1 homolog level in Chronic kidney disease with hypertension and no diabetes (17818_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein SGT1 in blood serum http://purl.obolibrary.org/obo/OBA_2043723 GCST90234821 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acylpyruvase FAHD1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17819_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fumarylacetoacetate hydrolase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041543 GCST90234822 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myeloid leukemia factor 1 level in Chronic kidney disease with hypertension and no diabetes (17820_170) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of myeloid leukemia factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042377 GCST90234823 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycylpeptide N-tetradecanoyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (17821_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycylpeptide N-tetradecanoyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042601 GCST90234824 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related and estrogen-regulated growth inhibitor level in Chronic kidney disease with hypertension and no diabetes (17822_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related and estrogen-regulated growth inhibitor in blood serum http://purl.obolibrary.org/obo/OBA_2043242 GCST90234825 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small nuclear ribonucleoprotein Sm D2 level in Chronic kidney disease with hypertension and no diabetes (17823_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small nuclear ribonucleoprotein Sm D2 in blood serum http://purl.obolibrary.org/obo/OBA_2043575 GCST90234826 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elongation factor 1-delta level in Chronic kidney disease with hypertension and no diabetes (17826_341) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of elongation factor 1-delta in blood serum http://purl.obolibrary.org/obo/OBA_2041419 GCST90234827 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynein light chain roadblock-type 2 level in Chronic kidney disease with hypertension and no diabetes (17827_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynein light chain roadblock-type 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041394 GCST90234828 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A14 level in Chronic kidney disease with hypertension and no diabetes (17828_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A14 in blood serum http://purl.obolibrary.org/obo/OBA_2043365 GCST90234829 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Three prime repair exonuclease 2 level in Chronic kidney disease with hypertension and no diabetes (17829_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of three prime repair exonuclease 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043929 GCST90234830 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isopentenyl-diphosphate delta-isomerase 2 level in Chronic kidney disease with hypertension and no diabetes (17832_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isopentenyl-diphosphate Delta-isomerase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041972 GCST90234831 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A13 level in Chronic kidney disease with hypertension and no diabetes (17835_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A13 in blood serum http://purl.obolibrary.org/obo/OBA_2040599 GCST90234832 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A16 level in Chronic kidney disease with hypertension and no diabetes (17836_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A16 in blood serum http://purl.obolibrary.org/obo/OBA_2043366 GCST90234833 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chloride intracellular channel protein 2 level in Chronic kidney disease with hypertension and no diabetes (17837_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chloride intracellular channel protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041048 GCST90234834 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphopantothenate--cysteine ligase level in Chronic kidney disease with hypertension and no diabetes (17843_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphopantothenate--cysteine ligase in blood serum http://purl.obolibrary.org/obo/OBA_2042983 GCST90234835 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Developmentally-regulated GTP-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (17849_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of developmentally-regulated GTP-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041363 GCST90234836 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Krueppel-like factor 4 level in Chronic kidney disease with hypertension and no diabetes (17850_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of krueppel-like factor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042118 GCST90234837 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase methylesterase 1 level in Chronic kidney disease with hypertension and no diabetes (17852_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase methylesterase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042998 GCST90234838 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-alpha-acetyltransferase 10 level in Chronic kidney disease with hypertension and no diabetes (17854_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-alpha-acetyltransferase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2040638 GCST90234839 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 4 level in Chronic kidney disease with hypertension and no diabetes (17855_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043261 GCST90234840 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5'(3')-deoxyribonucleotidase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17856_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5'(3')-deoxyribonucleotidase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042652 GCST90234841 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Long-chain specific acyl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17857_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of long-chain specific acyl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040468 GCST90234842 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like-conjugating enzyme ATG3 level in Chronic kidney disease with hypertension and no diabetes (18156_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like-conjugating enzyme ATG3 in blood serum http://purl.obolibrary.org/obo/OBA_2040717 GCST90234843 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-8 level in Chronic kidney disease with hypertension and no diabetes (18158_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 caspase-8 measurement http://www.ebi.ac.uk/efo/EFO_0010764 GCST90234844 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor-associated kinase 4 level in Chronic kidney disease with hypertension and no diabetes (18162_167) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-1 receptor-associated kinase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040325 GCST90234845 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 variant 2 level in Chronic kidney disease with hypertension and no diabetes (18165_181) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 variant 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044005 GCST90234846 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-related GTP-binding protein RhoB level in Chronic kidney disease with hypertension and no diabetes (18166_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-related GTP-binding protein RhoB in blood serum http://purl.obolibrary.org/obo/OBA_2043264 GCST90234847 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyrroline-5-carboxylate reductase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18170_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyrroline-5-carboxylate reductase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043123 GCST90234848 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sarcospan level in Chronic kidney disease with hypertension and no diabetes (23275_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sarcospan in blood serum http://purl.obolibrary.org/obo/OBA_2043665 GCST90236292 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0561 protein C2orf68 level in Chronic kidney disease with hypertension and no diabetes (23276_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UPF0561 protein C2orf68 in blood serum http://purl.obolibrary.org/obo/OBA_2044827 GCST90236293 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L12, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23278_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L12, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042423 GCST90236294 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Akirin-2 level in Chronic kidney disease with hypertension and no diabetes (23280_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of akirin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040545 GCST90236295 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 8A level in Chronic kidney disease with hypertension and no diabetes (23281_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 8A in blood serum http://purl.obolibrary.org/obo/OBA_2040675 GCST90236296 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-37 level in Chronic kidney disease with hypertension and no diabetes (23282_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-37 in blood serum http://purl.obolibrary.org/obo/OBA_2043155 GCST90236297 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-43 level in Chronic kidney disease with hypertension and no diabetes (23283_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Ras-related protein Rab-43 in blood serum http://purl.obolibrary.org/obo/OBA_2043163 GCST90236298 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LIM domain only transcription factor protein 4 level in Chronic kidney disease with hypertension and no diabetes (23284_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of LIM domain transcription factor LMO4 in blood serum http://purl.obolibrary.org/obo/OBA_2042213 GCST90236299 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD2 level in Chronic kidney disease with hypertension and no diabetes (23285_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD2 in blood serum http://purl.obolibrary.org/obo/OBA_2044463 GCST90236300 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 141 level in Chronic kidney disease with hypertension and no diabetes (23286_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RING finger protein 141 in blood serum http://purl.obolibrary.org/obo/OBA_2043291 GCST90236301 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (23287_109) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042543 GCST90236302 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 20 level in Chronic kidney disease with hypertension and no diabetes (23288_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 20 in blood serum http://purl.obolibrary.org/obo/OBA_2044574 GCST90236303 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurogenin-1 level in Chronic kidney disease with hypertension and no diabetes (23289_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurogenin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042566 GCST90236304 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Twinfilin-2 level in Chronic kidney disease with hypertension and no diabetes (23396_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of twinfilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043963 GCST90236380 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerase II subunit GRINL1A level in Chronic kidney disease with hypertension and no diabetes (23398_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerase II subunit GRINL1A in blood serum http://purl.obolibrary.org/obo/OBA_2044302 GCST90236381 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DAZ-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (23401_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DAZ-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041234 GCST90236382 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ganglioside-induced differentiation-associated protein 1-like 1 level in Chronic kidney disease with hypertension and no diabetes (23402_147) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ganglioside-induced differentiation-associated protein 1-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041696 GCST90236383 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cdc42 effector protein 4 level in Chronic kidney disease with hypertension and no diabetes (23403_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Cdc42 effector protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040955 GCST90236384 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HORMA domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (23405_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of HORMA domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044583 GCST90236385 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras association domain-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (23406_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras association domain-containing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043201 GCST90236386 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-acyl fatty acid synthase thioesterase, medium chain level in Chronic kidney disease with hypertension and no diabetes (23407_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of S-acyl fatty acid synthase thioesterase, medium chain in blood serum http://purl.obolibrary.org/obo/OBA_2042700 GCST90236387 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin 16 level in Chronic kidney disease with hypertension and no diabetes (23408_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-16 in blood serum http://purl.obolibrary.org/obo/OBA_2043586 GCST90236388 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptosomal-associated protein 29 level in Chronic kidney disease with hypertension and no diabetes (12357_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptosomal-associated protein 29 in blood serum http://purl.obolibrary.org/obo/OBA_2043564 GCST90233409 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (12358_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041988 GCST90233410 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein R-Ras2 level in Chronic kidney disease with hypertension and no diabetes (12361_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein R-Ras2 in blood serum http://purl.obolibrary.org/obo/OBA_2043344 GCST90233411 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin-like protein KIF16B level in Chronic kidney disease with hypertension and no diabetes (11672_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kinesin-like protein KIF16B in blood serum http://purl.obolibrary.org/obo/OBA_2042096 GCST90233348 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable palmitoyltransferase ZDHHC14 level in Chronic kidney disease with hypertension and no diabetes (11677_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of palmitoyltransferase ZDHHC14 in blood serum http://purl.obolibrary.org/obo/OBA_2044382 GCST90233349 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gap junction delta-2 protein level in Chronic kidney disease with hypertension and no diabetes (11678_105) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gap junction delta-2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041723 GCST90233350 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arf-GAP domain and FG repeat-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (11681_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Arf-GAP domain and FG repeat-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040535 GCST90233351 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin-interacting protein level in Chronic kidney disease with hypertension and no diabetes (11682_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thioredoxin-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043970 GCST90233352 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-binding protein GGA3 level in Chronic kidney disease with hypertension and no diabetes (11683_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-binding protein GGA3 in blood serum http://purl.obolibrary.org/obo/OBA_2041708 GCST90233353 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anaphase-promoting complex subunit 7 level in Chronic kidney disease with hypertension and no diabetes (11690_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anaphase-promoting complex subunit 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040588 GCST90233354 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SHC-transforming protein 4 level in Chronic kidney disease with hypertension and no diabetes (11692_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SHC-transforming protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040422 GCST90233355 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein tyrosine phosphatase type IVA 2 level in Chronic kidney disease with hypertension and no diabetes (11699_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein tyrosine phosphatase type IVA 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043098 GCST90233356 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lipocalin-1 level in Chronic kidney disease with hypertension and no diabetes (11708_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lipocalin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042172 GCST90233357 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carnitine O-palmitoyltransferase 1, muscle isoform level in Chronic kidney disease with hypertension and no diabetes (11709_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carnitine O-palmitoyltransferase 1, muscle isoform in blood serum http://purl.obolibrary.org/obo/OBA_2041126 GCST90233358 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein unc-45 homolog A level in Chronic kidney disease with hypertension and no diabetes (11712_207) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein unc-45 homolog A in blood serum http://purl.obolibrary.org/obo/OBA_2044036 GCST90233359 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. POU domain, class 2, transcription factor 1 level in Chronic kidney disease with hypertension and no diabetes (11715_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of POU domain, class 2, transcription factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042976 GCST90233360 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 S level in Chronic kidney disease with hypertension and no diabetes (17729_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 S in blood serum http://purl.obolibrary.org/obo/OBA_2044003 GCST90234762 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-aminobutyric acid receptor-associated protein level in Chronic kidney disease with hypertension and no diabetes (17735_130) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-aminobutyric acid receptor-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2041647 GCST90234763 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aprataxin level in Chronic kidney disease with hypertension and no diabetes (17736_105) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aprataxin in blood serum http://purl.obolibrary.org/obo/OBA_2040634 GCST90234764 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isovaleryl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17737_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isovaleryl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042066 GCST90234765 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cornulin level in Chronic kidney disease with hypertension and no diabetes (17738_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cornulin in blood serum http://purl.obolibrary.org/obo/OBA_2041150 GCST90234766 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17739_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hydroxyacyl-coenzyme A dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041833 GCST90234767 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein R-Ras level in Chronic kidney disease with hypertension and no diabetes (17742_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein R-Ras in blood serum http://purl.obolibrary.org/obo/OBA_2043343 GCST90234768 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 A level in Chronic kidney disease with hypertension and no diabetes (17743_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 A in blood serum http://purl.obolibrary.org/obo/OBA_2043989 GCST90234769 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial fission 1 protein level in Chronic kidney disease with hypertension and no diabetes (17746_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial fission 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041584 GCST90234770 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Quinone oxidoreductase PIG3 level in Chronic kidney disease with hypertension and no diabetes (17748_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of quinone oxidoreductase PIG3 in blood serum http://purl.obolibrary.org/obo/OBA_2044727 GCST90234771 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonucleoside-diphosphate reductase subunit M2 level in Chronic kidney disease with hypertension and no diabetes (17750_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonucleoside-diphosphate reductase subunit M2 in blood serum http://purl.obolibrary.org/obo/OBA_2043347 GCST90234772 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-crystallin B1 level in Chronic kidney disease with hypertension and no diabetes (17751_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-crystallin B1 in blood serum http://purl.obolibrary.org/obo/OBA_2041155 GCST90234773 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arginase-2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (17752_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arginase-2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040648 GCST90234774 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-glucose 6-dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (17755_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UDP-glucose 6-dehydrogenase in blood serum http://purl.obolibrary.org/obo/OBA_2044021 GCST90234775 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deoxycytidylate deaminase level in Chronic kidney disease with hypertension and no diabetes (17756_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deoxycytidylate deaminase in blood serum http://purl.obolibrary.org/obo/OBA_2041245 GCST90234776 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-binding protein 39 level in Chronic kidney disease with hypertension and no diabetes (17757_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-binding protein 39 in blood serum http://purl.obolibrary.org/obo/OBA_2040862 GCST90234777 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. L-xylulose reductase level in Chronic kidney disease with hypertension and no diabetes (17758_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of L-xylulose reductase in blood serum http://purl.obolibrary.org/obo/OBA_2041250 GCST90234778 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WD repeat-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (17760_128) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WD repeat-containing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044128 GCST90234779 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-sugar pyrophosphatase level in Chronic kidney disease with hypertension and no diabetes (17761_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-sugar pyrophosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2042672 GCST90234780 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-related GTP-binding protein RhoC level in Chronic kidney disease with hypertension and no diabetes (17764_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-related GTP-binding protein RhoC in blood serum http://purl.obolibrary.org/obo/OBA_2043265 GCST90234781 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Snurportin-1 level in Chronic kidney disease with hypertension and no diabetes (17765_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of snurportin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043581 GCST90234782 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil cytosol factor 1 level in Chronic kidney disease with hypertension and no diabetes (17766_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neutrophil cytosol factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042525 GCST90234783 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxyacid oxidase 1 level in Chronic kidney disease with hypertension and no diabetes (17768_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 2-hydroxyacid oxidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041836 GCST90234784 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PEST proteolytic signal-containing nuclear protein level in Chronic kidney disease with hypertension and no diabetes (17769_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PEST proteolytic signal-containing nuclear protein in blood serum http://purl.obolibrary.org/obo/OBA_2042801 GCST90234785 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ER membrane protein complex subunit 8 level in Chronic kidney disease with hypertension and no diabetes (17770_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ER membrane protein complex subunit 8 in blood serum http://purl.obolibrary.org/obo/OBA_2041106 GCST90234786 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Multivesicular body subunit 12B level in Chronic kidney disease with hypertension and no diabetes (23320_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of multivesicular body subunit 12B in blood serum http://purl.obolibrary.org/obo/OBA_2044384 GCST90236330 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 95 level in Chronic kidney disease with hypertension and no diabetes (23321_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of INO80 complex subunit E in blood serum http://purl.obolibrary.org/obo/OBA_2042028 GCST90236331 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Musculin level in Chronic kidney disease with hypertension and no diabetes (23322_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of musculin in blood serum http://purl.obolibrary.org/obo/OBA_2042438 GCST90236332 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity phosphatase DUPD1 level in Chronic kidney disease with hypertension and no diabetes (23323_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity phosphatase 29 in blood serum http://purl.obolibrary.org/obo/OBA_2041378 GCST90236333 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock protein beta-3 level in Chronic kidney disease with hypertension and no diabetes (23324_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock protein beta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041950 GCST90236334 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C16orf45 level in Chronic kidney disease with hypertension and no diabetes (23325_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bMERB domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044859 GCST90236335 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase A2 level in Chronic kidney disease with hypertension and no diabetes (23326_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase A2 in blood serum http://purl.obolibrary.org/obo/OBA_2041803 GCST90236336 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BLOC-1-related complex subunit 5 level in Chronic kidney disease with hypertension and no diabetes (23327_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BLOC-1-related complex subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042217 GCST90236337 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-4B level in Chronic kidney disease with hypertension and no diabetes (23329_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-4B in blood serum http://purl.obolibrary.org/obo/OBA_2043165 GCST90236338 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C22orf13 level in Chronic kidney disease with hypertension and no diabetes (23330_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein GUCD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044860 GCST90236339 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Late cornified envelope protein 3C level in Chronic kidney disease with hypertension and no diabetes (23334_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of late cornified envelope protein 3C in blood serum http://purl.obolibrary.org/obo/OBA_2042171 GCST90236340 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM229A level in Chronic kidney disease with hypertension and no diabetes (23335_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM229A in blood serum http://purl.obolibrary.org/obo/OBA_2044819 GCST90236341 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative potassium channel regulatory protein level in Chronic kidney disease with hypertension and no diabetes (23336_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of potassium channel regulatory protein in blood serum http://purl.obolibrary.org/obo/OBA_2044317 GCST90236342 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 level in Chronic kidney disease with hypertension and no diabetes (23337_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing adapter for CUL3-mediated RhoA degradation protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044254 GCST90236343 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor 24 level in Chronic kidney disease with hypertension and no diabetes (23339_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor 24 in blood serum http://purl.obolibrary.org/obo/OBA_2044396 GCST90236344 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming growth factor beta-1 level in Chronic kidney disease with hypertension and no diabetes (2333_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 transforming growth factor beta-1 measurement http://www.ebi.ac.uk/efo/EFO_0020780 GCST90236345 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methylthioribose-1-phosphate isomerase level in Chronic kidney disease with hypertension and no diabetes (23340_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methylthioribose-1-phosphate isomerase in blood serum http://purl.obolibrary.org/obo/OBA_2042418 GCST90236346 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Meiotic recombination protein DMC1/LIM15 homolog level in Chronic kidney disease with hypertension and no diabetes (23341_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of meiotic recombination protein DMC1/LIM15 in blood serum http://purl.obolibrary.org/obo/OBA_2041321 GCST90236347 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein rogdi homolog level in Chronic kidney disease with hypertension and no diabetes (23343_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein rogdi in blood serum http://purl.obolibrary.org/obo/OBA_2043307 GCST90236348 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-terminal EF-hand calcium-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (23345_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-terminal EF-hand calcium-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042548 GCST90236349 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM118B level in Chronic kidney disease with hypertension and no diabetes (23350_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM118B in blood serum http://purl.obolibrary.org/obo/OBA_2044293 GCST90236350 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dysbindin level in Chronic kidney disease with hypertension and no diabetes (23352_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dysbindin in blood serum http://purl.obolibrary.org/obo/OBA_2041374 GCST90236351 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 24 level in Chronic kidney disease with hypertension and no diabetes (23356_32) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of coiled-coil domain-containing protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2044666 GCST90236352 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM118A level in Chronic kidney disease with hypertension and no diabetes (23358_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM118A in blood serum http://purl.obolibrary.org/obo/OBA_2044589 GCST90236353 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-mRNA-splicing regulator WTAP level in Chronic kidney disease with hypertension and no diabetes (23359_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pre-mRNA-splicing regulator WTAP in blood serum http://purl.obolibrary.org/obo/OBA_2044144 GCST90236354 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0193 protein EVG1 level in Chronic kidney disease with hypertension and no diabetes (23273_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UPF0193 protein EVG1 in blood serum http://purl.obolibrary.org/obo/OBA_2044867 GCST90236290 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EF-hand calcium-binding domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (23274_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calaxin in blood serum http://purl.obolibrary.org/obo/OBA_2044392 GCST90236291 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1 regulatory subunit 1A level in Chronic kidney disease with hypertension and no diabetes (17706_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1 regulatory subunit 1A in blood serum http://purl.obolibrary.org/obo/OBA_2043002 GCST90234752 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor protein D53 level in Chronic kidney disease with hypertension and no diabetes (17710_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor protein D53 in blood serum http://purl.obolibrary.org/obo/OBA_2043907 GCST90234753 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-associated membrane protein 1 level in Chronic kidney disease with hypertension and no diabetes (17711_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-associated membrane protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044075 GCST90234754 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isopentenyl-diphosphate Delta-isomerase 1 level in Chronic kidney disease with hypertension and no diabetes (17712_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isopentenyl-diphosphate Delta-isomerase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041971 GCST90234755 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth arrest-specific protein 7 level in Chronic kidney disease with hypertension and no diabetes (17721_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth arrest-specific protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041675 GCST90234756 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WW domain-containing oxidoreductase level in Chronic kidney disease with hypertension and no diabetes (17724_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WW domain-containing oxidoreductase in blood serum http://purl.obolibrary.org/obo/OBA_2040234 GCST90234757 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Harmonin level in Chronic kidney disease with hypertension and no diabetes (17725_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of harmonin in blood serum http://purl.obolibrary.org/obo/OBA_2044050 GCST90234758 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein SAR1a level in Chronic kidney disease with hypertension and no diabetes (17726_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein SAR1a in blood serum http://purl.obolibrary.org/obo/OBA_2043380 GCST90234759 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Securin level in Chronic kidney disease with hypertension and no diabetes (17727_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of securin in blood serum http://purl.obolibrary.org/obo/OBA_2043114 GCST90234760 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Charged multivesicular body protein 2a level in Chronic kidney disease with hypertension and no diabetes (17728_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of charged multivesicular body protein 2a in blood serum http://purl.obolibrary.org/obo/OBA_2041010 GCST90234761 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Obestatin level in Chronic kidney disease with hypertension and no diabetes (23581_131) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of appetite-regulating hormone in blood serum http://purl.obolibrary.org/obo/OBA_2041716 GCST90236445 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleotide triphosphate diphosphatase NUDT15 level in Chronic kidney disease with hypertension and no diabetes (23584_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleotide triphosphate diphosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2044510 GCST90236446 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cancer/testis antigen 1B level in Chronic kidney disease with hypertension and no diabetes (23586_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cancer/testis antigen 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041181 GCST90236447 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxysteroid dehydrogenase-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (23588_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of hydroxysteroid dehydrogenase-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041941 GCST90236448 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1 regulatory subunit 27 level in Chronic kidney disease with hypertension and no diabetes (23589_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dysferlin-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041399 GCST90236449 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor receptor 3 level in Chronic kidney disease with hypertension and no diabetes (2358_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 vascular endothelial growth factor receptor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008315 GCST90236450 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. piRNA biogenesis protein EXD1 level in Chronic kidney disease with hypertension and no diabetes (23591_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of piRNA biogenesis protein EXD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044622 GCST90236451 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein MB21D2 level in Chronic kidney disease with hypertension and no diabetes (23593_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleotidyltransferase MB21D2 in blood serum http://purl.obolibrary.org/obo/OBA_2044534 GCST90236452 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor 2C2-associated protein level in Chronic kidney disease with hypertension and no diabetes (23594_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor 2C2-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2042631 GCST90236453 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Laccase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (23595_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of purine nucleoside phosphorylase LACC1 in blood serum http://purl.obolibrary.org/obo/OBA_2044472 GCST90236454 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 89 level in Chronic kidney disease with hypertension and no diabetes (23596_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 89 in blood serum http://purl.obolibrary.org/obo/OBA_2044765 GCST90236455 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arf-GAP domain and FG repeat-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (23597_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Arf-GAP domain and FG repeat-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044252 GCST90236456 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-coenzyme A thioesterase 12 level in Chronic kidney disease with hypertension and no diabetes (23601_43) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of acetyl-coenzyme A thioesterase in blood serum http://purl.obolibrary.org/obo/OBA_2040480 GCST90236457 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D level in Chronic kidney disease with hypertension and no diabetes (23602_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acyl-phosphatidylethanolamine-hydrolyzing phospholipase D in blood serum http://purl.obolibrary.org/obo/OBA_2042510 GCST90236458 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-complex protein 11-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (23605_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-complex protein 11-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043818 GCST90236459 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sterile alpha motif domain-containing protein 4B level in Chronic kidney disease with hypertension and no diabetes (23606_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Smaug homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044359 GCST90236460 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C16orf71 level in Chronic kidney disease with hypertension and no diabetes (23607_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynein axonemal assembly factor 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044841 GCST90236461 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MARVEL domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (23611_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MARVEL domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042302 GCST90236462 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TRM112-like protein level in Chronic kidney disease with hypertension and no diabetes (23615_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of multifunctional methyltransferase subunit TRM112-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2044371 GCST90236463 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Huntingtin-interacting protein K level in Chronic kidney disease with hypertension and no diabetes (23617_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of huntingtin-interacting protein K in blood serum http://purl.obolibrary.org/obo/OBA_2041964 GCST90236464 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 593 level in Chronic kidney disease with hypertension and no diabetes (23618_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 593 in blood serum http://purl.obolibrary.org/obo/OBA_2044211 GCST90236465 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leydig cell tumor 10 kDa protein homolog level in Chronic kidney disease with hypertension and no diabetes (23619_235) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leydig cell tumor 10 kDa protein in blood serum http://purl.obolibrary.org/obo/OBA_2041223 GCST90236466 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CapZ-interacting protein level in Chronic kidney disease with hypertension and no diabetes (23620_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Capz-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043221 GCST90236467 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit Tim13 level in Chronic kidney disease with hypertension and no diabetes (23621_326) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import inner membrane translocase subunit Tim13 in blood serum http://purl.obolibrary.org/obo/OBA_2043853 GCST90236468 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SOSS complex subunit C level in Chronic kidney disease with hypertension and no diabetes (23622_128) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of SOSS complex subunit C in blood serum http://purl.obolibrary.org/obo/OBA_2044598 GCST90236469 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 63 level in Chronic kidney disease with hypertension and no diabetes (23424_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 63 in blood serum http://purl.obolibrary.org/obo/OBA_2044621 GCST90236395 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ermin level in Chronic kidney disease with hypertension and no diabetes (23425_19) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of ermin in blood serum http://purl.obolibrary.org/obo/OBA_2041506 GCST90236396 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Variable charge X-linked protein 1 level in Chronic kidney disease with hypertension and no diabetes (23426_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of variable charge X-linked protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044092 GCST90236397 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM151B level in Chronic kidney disease with hypertension and no diabetes (23518_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM151B in blood serum http://purl.obolibrary.org/obo/OBA_2044603 GCST90236398 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-lactamase-like protein FLJ75971 level in Chronic kidney disease with hypertension and no diabetes (23520_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-coenzyme A thioesterase MBLAC2 in blood serum http://purl.obolibrary.org/obo/OBA_2044555 GCST90236399 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleoside diphosphate kinase 7 level in Chronic kidney disease with hypertension and no diabetes (23521_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleoside diphosphate kinase 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042596 GCST90236400 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTPase IMAP family member GIMD1 level in Chronic kidney disease with hypertension and no diabetes (23522_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTPase IMAP family member GIMD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044494 GCST90236401 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM49A level in Chronic kidney disease with hypertension and no diabetes (23523_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CYFIP-related Rac1 interactor A in blood serum http://purl.obolibrary.org/obo/OBA_2044523 GCST90236402 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein N-terminal asparagine amidohydrolase level in Chronic kidney disease with hypertension and no diabetes (23524_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein N-terminal asparagine amidohydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2042653 GCST90236403 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nitric oxide synthase-interacting protein level in Chronic kidney disease with hypertension and no diabetes (23525_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nitric oxide synthase-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2042608 GCST90236404 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein KTI12 homolog level in Chronic kidney disease with hypertension and no diabetes (23526_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein KTI12 in blood serum http://purl.obolibrary.org/obo/OBA_2042151 GCST90236405 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phytanoyl-CoA hydroxylase-interacting protein-like level in Chronic kidney disease with hypertension and no diabetes (23528_199) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phytanoyl-CoA hydroxylase-interacting protein-like in blood serum http://purl.obolibrary.org/obo/OBA_2042883 GCST90236406 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. StAR-related lipid transfer protein 7, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23529_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of StAR-related lipid transfer protein 7, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043694 GCST90236407 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomodulin-4 level in Chronic kidney disease with hypertension and no diabetes (23530_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tropomodulin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043880 GCST90236408 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hematopoietic SH2 domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (23531_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hematopoietic SH2 domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2041943 GCST90236409 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM45A level in Chronic kidney disease with hypertension and no diabetes (23535_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DENN domain-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044295 GCST90236410 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C19orf84 level in Chronic kidney disease with hypertension and no diabetes (23536_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C19orf84 in blood serum http://purl.obolibrary.org/obo/OBA_2044887 GCST90236411 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor Sp6 level in Chronic kidney disease with hypertension and no diabetes (23537_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor Sp6 in blood serum http://purl.obolibrary.org/obo/OBA_2043605 GCST90236412 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CDK-activating kinase assembly factor MAT1 level in Chronic kidney disease with hypertension and no diabetes (23540_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CDK-activating kinase assembly factor MAT1 in blood serum http://purl.obolibrary.org/obo/OBA_2042392 GCST90236413 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Citrate lyase subunit beta-like protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23541_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of citramalyl-CoA lyase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041062 GCST90236414 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Golgi phosphoprotein 3-like level in Chronic kidney disease with hypertension and no diabetes (23542_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Golgi phosphoprotein 3-like in blood serum http://purl.obolibrary.org/obo/OBA_2041764 GCST90236415 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable tRNA pseudouridine synthase 1 level in Chronic kidney disease with hypertension and no diabetes (23543_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pseudouridylate synthase TRUB1 in blood serum http://purl.obolibrary.org/obo/OBA_2044374 GCST90236416 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-complex protein 10A homolog level in Chronic kidney disease with hypertension and no diabetes (23544_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90236417 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear distribution protein nudE-like 1 level in Chronic kidney disease with hypertension and no diabetes (23545_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear distribution protein nudE-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042534 GCST90236418 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxyacylglutathione hydrolase-like protein level in Chronic kidney disease with hypertension and no diabetes (23546_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hydroxyacylglutathione hydrolase-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2041835 GCST90236419 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein 3 level in Chronic kidney disease with hypertension and no diabetes (23547_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043803 GCST90236420 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratinocyte differentiation factor 1 level in Chronic kidney disease with hypertension and no diabetes (23550_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratinocyte differentiation factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044846 GCST90236421 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional adapter 3 level in Chronic kidney disease with hypertension and no diabetes (23551_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional adapter 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043768 GCST90236422 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ABI gene family member 3 level in Chronic kidney disease with hypertension and no diabetes (23553_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ABI gene family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040461 GCST90236423 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH2 domain-containing adapter protein D level in Chronic kidney disease with hypertension and no diabetes (23554_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH2 domain-containing adapter protein D in blood serum http://purl.obolibrary.org/obo/OBA_2043500 GCST90236424 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein RAD level in Chronic kidney disease with hypertension and no diabetes (23555_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein RAD in blood serum http://purl.obolibrary.org/obo/OBA_2043341 GCST90236425 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription cofactor vestigial-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (23556_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription cofactor vestigial-like protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044096 GCST90236426 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. F-actin-capping protein subunit beta level in Chronic kidney disease with hypertension and no diabetes (23557_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of F-actin-capping protein subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040896 GCST90236427 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methyltransferase-like protein 2B level in Chronic kidney disease with hypertension and no diabetes (23558_33) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tRNA N(3)-methylcytidine methyltransferase METTL2B in blood serum http://purl.obolibrary.org/obo/OBA_2042346 GCST90236428 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DDRGK domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (23559_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DDRGK domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044542 GCST90236429 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centrosomal protein of 41 kDa level in Chronic kidney disease with hypertension and no diabetes (23560_154) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centrosomal protein of 41 kDa in blood serum http://purl.obolibrary.org/obo/OBA_2043948 GCST90236430 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 97 level in Chronic kidney disease with hypertension and no diabetes (23561_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 97 in blood serum http://purl.obolibrary.org/obo/OBA_2044266 GCST90236431 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-lysine methyltransferase METTL21C level in Chronic kidney disease with hypertension and no diabetes (23564_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-lysine methyltransferase METTL21C in blood serum http://purl.obolibrary.org/obo/OBA_2044538 GCST90236432 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein-L2 level in Chronic kidney disease with hypertension and no diabetes (23566_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of apolipoprotein L2 in blood serum http://purl.obolibrary.org/obo/OBA_2040630 GCST90236433 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein G(q) subunit alpha level in Chronic kidney disease with hypertension and no diabetes (23567_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide-binding protein G(q) subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041749 GCST90236434 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein Meis2 level in Chronic kidney disease with hypertension and no diabetes (23568_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein Meis2 in blood serum http://purl.obolibrary.org/obo/OBA_2042334 GCST90236435 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. START domain-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (23569_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of START domain-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043692 GCST90236436 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein with KRAB and SCAN domains 7 level in Chronic kidney disease with hypertension and no diabetes (23570_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein with KRAB and SCAN domains 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044189 GCST90236437 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 94 level in Chronic kidney disease with hypertension and no diabetes (23571_93) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of splicing factor YJU2 in blood serum http://purl.obolibrary.org/obo/OBA_2044265 GCST90236438 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA wybutosine-synthesizing protein 3 homolog level in Chronic kidney disease with hypertension and no diabetes (23572_186) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tRNA wybutosine-synthesizing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043977 GCST90236439 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase assembly protein COX19 level in Chronic kidney disease with hypertension and no diabetes (23575_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome c oxidase assembly protein COX19 in blood serum http://purl.obolibrary.org/obo/OBA_2041104 GCST90236440 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein BEX4 level in Chronic kidney disease with hypertension and no diabetes (23576_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein BEX4 in blood serum http://purl.obolibrary.org/obo/OBA_2040795 GCST90236441 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small integral membrane protein 3 level in Chronic kidney disease with hypertension and no diabetes (23578_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small integral membrane protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044868 GCST90236442 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kita-kyushu lung cancer antigen 1 level in Chronic kidney disease with hypertension and no diabetes (23579_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Kita-kyushu lung cancer antigen 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042113 GCST90236443 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proline-rich protein 15 level in Chronic kidney disease with hypertension and no diabetes (23580_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proline-rich protein 15 in blood serum http://purl.obolibrary.org/obo/OBA_2043043 GCST90236444 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aflatoxin B1 aldehyde reductase member 3 level in Chronic kidney disease with hypertension and no diabetes (18173_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aflatoxin B1 aldehyde reductase member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040554 GCST90234851 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death 6-interacting protein level in Chronic kidney disease with hypertension and no diabetes (18174_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of programmed cell death 6-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2042815 GCST90234852 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptic vesicle membrane protein VAT-1 homolog level in Chronic kidney disease with hypertension and no diabetes (18175_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptic vesicle membrane protein VAT-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044084 GCST90234853 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD8-activating enzyme E1 regulatory subunit level in Chronic kidney disease with hypertension and no diabetes (18177_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD8-activating enzyme E1 regulatory subunit in blood serum http://purl.obolibrary.org/obo/OBA_2042499 GCST90234854 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (18178_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2043383 GCST90234855 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermine synthase level in Chronic kidney disease with hypertension and no diabetes (18179_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spermine synthase in blood serum http://purl.obolibrary.org/obo/OBA_2043560 GCST90234856 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Reticulon-4-interacting protein 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18180_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of reticulon-4-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043353 GCST90234857 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein TSSC4 level in Chronic kidney disease with hypertension and no diabetes (18181_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein TSSC4 in blood serum http://purl.obolibrary.org/obo/OBA_2043951 GCST90234858 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoenolpyruvate carboxykinase, cytosolic [GTP] level in Chronic kidney disease with hypertension and no diabetes (18182_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoenolpyruvate carboxykinase, cytosolic [GTP] in blood serum http://purl.obolibrary.org/obo/OBA_2042799 GCST90234859 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low density lipoprotein receptor adapter protein 1 level in Chronic kidney disease with hypertension and no diabetes (18183_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low density lipoprotein receptor adapter protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042183 GCST90234860 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fructose-bisphosphate aldolase B level in Chronic kidney disease with hypertension and no diabetes (18185_118) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fructose-bisphosphate aldolase B in blood serum http://purl.obolibrary.org/obo/OBA_2040567 GCST90234861 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Threonine--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (18186_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of threonine--tRNA ligase 1, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2043779 GCST90234862 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartoacylase level in Chronic kidney disease with hypertension and no diabetes (18187_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aspartoacylase in blood serum http://purl.obolibrary.org/obo/OBA_2040704 GCST90234863 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycine amidinotransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18188_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycine amidinotransferase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041676 GCST90234864 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein-sorting-associated protein 25 level in Chronic kidney disease with hypertension and no diabetes (18189_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vacuolar protein-sorting-associated protein 25 in blood serum http://purl.obolibrary.org/obo/OBA_2044107 GCST90234865 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase recruitment domain-containing protein 18 level in Chronic kidney disease with hypertension and no diabetes (18190_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caspase recruitment domain-containing protein 18 in blood serum http://purl.obolibrary.org/obo/OBA_2040898 GCST90234866 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ran-specific GTPase-activating protein level in Chronic kidney disease with hypertension and no diabetes (18191_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ran-specific GTPase-activating protein in blood serum http://purl.obolibrary.org/obo/OBA_2043190 GCST90234867 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 5 level in Chronic kidney disease with hypertension and no diabetes (18192_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative melanoma-associated antigen 5P in blood serum http://purl.obolibrary.org/obo/OBA_2042267 GCST90234868 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mortality factor 4-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (18193_165) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mortality factor 4-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042401 GCST90234869 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein 9 level in Chronic kidney disease with hypertension and no diabetes (18194_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fatty acid-binding protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2041540 GCST90234870 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oral cancer-overexpressed protein 1 level in Chronic kidney disease with hypertension and no diabetes (18195_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein LTO1 homolog in blood serum http://purl.obolibrary.org/obo/OBA_2042709 GCST90234871 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Afamin level in Chronic kidney disease with hypertension and no diabetes (18196_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 afamin measurement http://www.ebi.ac.uk/efo/EFO_0008015 GCST90234872 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Creatine kinase S-type, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18197_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of creatine kinase S-type, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041038 GCST90234873 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemoglobin subunit theta-1 level in Chronic kidney disease with hypertension and no diabetes (18198_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hemoglobin subunit theta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041842 GCST90234874 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte antigen CD37 level in Chronic kidney disease with hypertension and no diabetes (18202_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD37 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040945 GCST90234875 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-crystallin C level in Chronic kidney disease with hypertension and no diabetes (18203_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of gamma-crystallin C in blood serum http://purl.obolibrary.org/obo/OBA_2041159 GCST90234876 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein 1 level in Chronic kidney disease with hypertension and no diabetes (18204_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043801 GCST90234877 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 6 level in Chronic kidney disease with hypertension and no diabetes (18205_123) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042268 GCST90234878 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase 6 level in Chronic kidney disease with hypertension and no diabetes (18206_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alcohol dehydrogenase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040518 GCST90234879 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Charged multivesicular body protein 1b level in Chronic kidney disease with hypertension and no diabetes (18207_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of charged multivesicular body protein 1b in blood serum http://purl.obolibrary.org/obo/OBA_2041009 GCST90234880 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G2/mitotic-specific cyclin-B2 level in Chronic kidney disease with hypertension and no diabetes (18208_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of G2/mitotic-specific cyclin-B2 in blood serum http://purl.obolibrary.org/obo/OBA_2040934 GCST90234881 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spindlin-1 level in Chronic kidney disease with hypertension and no diabetes (18210_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spindlin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043627 GCST90234882 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase Mu 5 level in Chronic kidney disease with hypertension and no diabetes (18212_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase mu 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041807 GCST90234883 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD8-conjugating enzyme UBE2F level in Chronic kidney disease with hypertension and no diabetes (18213_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD8-conjugating enzyme UBE2F in blood serum http://purl.obolibrary.org/obo/OBA_2044600 GCST90234884 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate--cysteine ligase regulatory subunit level in Chronic kidney disease with hypertension and no diabetes (18214_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutamate--cysteine ligase regulatory subunit in blood serum http://purl.obolibrary.org/obo/OBA_2041689 GCST90234885 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable tRNA(His) guanylyltransferase level in Chronic kidney disease with hypertension and no diabetes (18215_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of probable tRNA(His) guanylyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044366 GCST90234886 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-11 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (18216_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-11 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020491 GCST90234887 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CB1 cannabinoid receptor-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (18218_48) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of CB1 cannabinoid receptor-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041072 GCST90234888 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Steroid receptor RNA activator 1 level in Chronic kidney disease with hypertension and no diabetes (18220_141) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of steroid receptor RNA activator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043650 GCST90234889 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endophilin-B2 level in Chronic kidney disease with hypertension and no diabetes (18222_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endophilin-B2 in blood serum http://purl.obolibrary.org/obo/OBA_2043494 GCST90234890 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Charged multivesicular body protein 1a level in Chronic kidney disease with hypertension and no diabetes (18224_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of charged multivesicular body protein 1a in blood serum http://purl.obolibrary.org/obo/OBA_2041008 GCST90234891 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heme-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (18225_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of heme-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041853 GCST90234892 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase subunit 5A, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18226_148) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome c oxidase subunit 5A, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041107 GCST90234893 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 2-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (18227_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 2-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040967 GCST90234894 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleolar protein 16 level in Chronic kidney disease with hypertension and no diabetes (18228_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleolar protein 16 in blood serum http://purl.obolibrary.org/obo/OBA_2042606 GCST90234895 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prion-like protein doppel level in Chronic kidney disease with hypertension and no diabetes (18231_147) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prion-like protein doppel in blood serum http://purl.obolibrary.org/obo/OBA_2043034 GCST90234896 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 5-phosphate 4-kinase type-2 beta level in Chronic kidney disease with hypertension and no diabetes (18232_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol 5-phosphate 4-kinase type-2 beta in blood serum http://purl.obolibrary.org/obo/OBA_2042898 GCST90234897 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartate aminotransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18233_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of aspartate aminotransferase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041767 GCST90234898 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycerol-3-phosphate phosphatase level in Chronic kidney disease with hypertension and no diabetes (18235_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90234899 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-related protein level in Chronic kidney disease with hypertension and no diabetes (18236_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of galectin-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2044325 GCST90234900 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor-interacting protein 3 level in Chronic kidney disease with hypertension and no diabetes (18237_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor-interacting protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042640 GCST90234901 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Olfactory marker protein level in Chronic kidney disease with hypertension and no diabetes (18240_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of olfactory marker protein in blood serum http://purl.obolibrary.org/obo/OBA_2042707 GCST90234902 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18241_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041125 GCST90234903 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm surface protein Sp17 level in Chronic kidney disease with hypertension and no diabetes (18242_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm surface protein Sp17 in blood serum http://purl.obolibrary.org/obo/OBA_2043606 GCST90234904 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UMP-CMP kinase level in Chronic kidney disease with hypertension and no diabetes (18243_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 UMP-CMP kinase measurement http://www.ebi.ac.uk/efo/EFO_0008313 GCST90234905 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A7 level in Chronic kidney disease with hypertension and no diabetes (18244_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A7 in blood serum http://purl.obolibrary.org/obo/OBA_2040602 GCST90234906 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Single-stranded DNA-binding protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18253_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of single-stranded DNA-binding protein, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043663 GCST90234907 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH-cytochrome b5 reductase 1 level in Chronic kidney disease with hypertension and no diabetes (18255_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH-cytochrome b5 reductase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041210 GCST90234908 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal recognition particle 19 kDa protein level in Chronic kidney disease with hypertension and no diabetes (18257_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal recognition particle 19 kDa protein in blood serum http://purl.obolibrary.org/obo/OBA_2043658 GCST90234909 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein MOX-2 level in Chronic kidney disease with hypertension and no diabetes (18259_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein MOX-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042338 GCST90234910 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein NATD1 level in Chronic kidney disease with hypertension and no diabetes (18261_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein NATD1 in blood serum http://purl.obolibrary.org/obo/OBA_2041817 GCST90234911 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 25 level in Chronic kidney disease with hypertension and no diabetes (18264_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 25 in blood serum http://purl.obolibrary.org/obo/OBA_2044261 GCST90234912 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 34 level in Chronic kidney disease with hypertension and no diabetes (18265_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 34 in blood serum http://purl.obolibrary.org/obo/OBA_2044202 GCST90234913 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase recruitment domain-containing protein 17 level in Chronic kidney disease with hypertension and no diabetes (18267_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative caspase recruitment domain-containing protein 17P in blood serum http://purl.obolibrary.org/obo/OBA_2040897 GCST90234914 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G antigen 2A level in Chronic kidney disease with hypertension and no diabetes (18268_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of G antigen 2A in blood serum http://purl.obolibrary.org/obo/OBA_2044493 GCST90234915 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription initiation factor TFIID subunit 10 level in Chronic kidney disease with hypertension and no diabetes (18270_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription initiation factor TFIID subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043769 GCST90234916 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18271_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 3-oxoacyl-[acyl-carrier-protein] synthase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042727 GCST90234917 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G antigen 2D level in Chronic kidney disease with hypertension and no diabetes (18273_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of G antigen 2D in blood serum http://purl.obolibrary.org/obo/OBA_2041654 GCST90234918 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small EDRK-rich factor 2 level in Chronic kidney disease with hypertension and no diabetes (18274_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small EDRK-rich factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043455 GCST90234919 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich protein 1 level in Chronic kidney disease with hypertension and no diabetes (18275_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cysteine-rich protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041141 GCST90234920 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell leukemia/lymphoma protein 1B level in Chronic kidney disease with hypertension and no diabetes (18276_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-cell leukemia/lymphoma protein 1B in blood serum http://purl.obolibrary.org/obo/OBA_2043814 GCST90234921 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TP53-regulated inhibitor of apoptosis 1 level in Chronic kidney disease with hypertension and no diabetes (18277_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TP53-regulated inhibitor of apoptosis 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043931 GCST90234922 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative D-tyrosyl-tRNA(Tyr) deacylase 2 level in Chronic kidney disease with hypertension and no diabetes (18280_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of D-aminoacyl-tRNA deacylase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044855 GCST90234923 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-11 level in Chronic kidney disease with hypertension and no diabetes (18282_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-11 in blood serum http://purl.obolibrary.org/obo/OBA_2041752 GCST90234924 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein KIBRA level in Chronic kidney disease with hypertension and no diabetes (18284_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein WWC1 in blood serum http://purl.obolibrary.org/obo/OBA_2044145 GCST90234925 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase CBL level in Chronic kidney disease with hypertension and no diabetes (12016_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase CBL in blood serum http://purl.obolibrary.org/obo/OBA_2040911 GCST90233386 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thiamin pyrophosphokinase 1 level in Chronic kidney disease with hypertension and no diabetes (12018_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thiamin pyrophosphokinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043910 GCST90233387 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bisphosphoglycerate mutase level in Chronic kidney disease with hypertension and no diabetes (12020_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bisphosphoglycerate mutase in blood serum http://purl.obolibrary.org/obo/OBA_2040819 GCST90233388 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mothers against decapentaplegic homolog 4 level in Chronic kidney disease with hypertension and no diabetes (12022_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of smad4 in blood serum http://purl.obolibrary.org/obo/OBA_2040202 GCST90233389 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmin level in Chronic kidney disease with hypertension and no diabetes (12030_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of desmin in blood serum http://purl.obolibrary.org/obo/OBA_2041289 GCST90233390 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitotic checkpoint serine/threonine-protein kinase BUB1 level in Chronic kidney disease with hypertension and no diabetes (12033_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitotic checkpoint serine/threonine-protein kinase BUB1 in blood serum http://purl.obolibrary.org/obo/OBA_2040839 GCST90233391 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TAR DNA-binding protein 43 level in Chronic kidney disease with hypertension and no diabetes (12046_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TAR DNA-binding protein 43 in blood serum http://purl.obolibrary.org/obo/OBA_2043778 GCST90233392 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth/differentiation factor 8 level in Chronic kidney disease with hypertension and no diabetes (12077_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 growth/differentiation factor 8 measurement http://www.ebi.ac.uk/efo/EFO_0021960 GCST90233393 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosomal protein S6 kinase alpha-1 level in Chronic kidney disease with hypertension and no diabetes (12329_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ribosomal protein S6 kinase alpha-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043338 GCST90233394 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribose-5-phosphate isomerase level in Chronic kidney disease with hypertension and no diabetes (12333_87) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ribose-5-phosphate isomerase in blood serum http://purl.obolibrary.org/obo/OBA_2043317 GCST90233395 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine hydroxymethyltransferase, cytosolic level in Chronic kidney disease with hypertension and no diabetes (12334_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine hydroxymethyltransferase, cytosolic in blood serum http://purl.obolibrary.org/obo/OBA_2043503 GCST90233396 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pikachurin level in Chronic kidney disease with hypertension and no diabetes (12338_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pikachurin in blood serum http://purl.obolibrary.org/obo/OBA_2041426 GCST90233397 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alanine--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (12340_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of alanine--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2040455 GCST90233398 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 6 level in Chronic kidney disease with hypertension and no diabetes (12341_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041389 GCST90233399 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (12343_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040473 GCST90233400 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anaphase-promoting complex subunit 10 level in Chronic kidney disease with hypertension and no diabetes (12345_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anaphase-promoting complex subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2040587 GCST90233401 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cerebral cavernous malformations 2 protein level in Chronic kidney disease with hypertension and no diabetes (12347_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cerebral cavernous malformations 2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2040930 GCST90233402 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine--tRNA ligase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12348_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine--tRNA ligase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043384 GCST90233403 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein C-ets-2 level in Chronic kidney disease with hypertension and no diabetes (12350_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein C-ets-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041517 GCST90233404 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal transducer and activator of transcription 1-alpha/beta level in Chronic kidney disease with hypertension and no diabetes (12351_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 signal transducer and activator of transcription 1-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0021915 GCST90233405 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arrestin domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (12352_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arrestin domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044768 GCST90233406 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosome-recycling factor, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12355_223) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosome-recycling factor, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042435 GCST90233407 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorcin level in Chronic kidney disease with hypertension and no diabetes (12356_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorcin in blood serum http://purl.obolibrary.org/obo/OBA_2043654 GCST90233408 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 11 level in Chronic kidney disease with hypertension and no diabetes (18171_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-X-C motif chemokine 11 measurement http://www.ebi.ac.uk/efo/EFO_0008057 GCST90234849 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone chaperone ASF1A level in Chronic kidney disease with hypertension and no diabetes (18172_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone chaperone ASF1A in blood serum http://purl.obolibrary.org/obo/OBA_2040696 GCST90234850 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small VCP/p97-interacting protein level in Chronic kidney disease with hypertension and no diabetes (18285_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small VCP/p97-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043740 GCST90234926 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ZW10 interactor level in Chronic kidney disease with hypertension and no diabetes (18286_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ZW10 interactor in blood serum http://purl.obolibrary.org/obo/OBA_2044223 GCST90234927 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 15 level in Chronic kidney disease with hypertension and no diabetes (18289_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 15 measurement http://www.ebi.ac.uk/efo/EFO_0008043 GCST90234928 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A8 level in Chronic kidney disease with hypertension and no diabetes (18290_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of annexin A8 in blood serum http://purl.obolibrary.org/obo/OBA_2040603 GCST90234929 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase inhibitor 1 level in Chronic kidney disease with hypertension and no diabetes (18291_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase inhibitor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040970 GCST90234930 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor SOX-2 level in Chronic kidney disease with hypertension and no diabetes (18294_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor SOX-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043602 GCST90234931 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glyoxylate reductase/hydroxypyruvate reductase level in Chronic kidney disease with hypertension and no diabetes (18295_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glyoxylate reductase/hydroxypyruvate reductase in blood serum http://purl.obolibrary.org/obo/OBA_2041787 GCST90234932 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein M-Ras level in Chronic kidney disease with hypertension and no diabetes (18297_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein M-Ras in blood serum http://purl.obolibrary.org/obo/OBA_2042414 GCST90234933 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpain small subunit 1 level in Chronic kidney disease with hypertension and no diabetes (18299_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calpain small subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040892 GCST90234934 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional activator protein Pur-beta level in Chronic kidney disease with hypertension and no diabetes (18300_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional activator protein Pur-beta in blood serum http://purl.obolibrary.org/obo/OBA_2043117 GCST90234935 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear apoptosis-inducing factor 1 level in Chronic kidney disease with hypertension and no diabetes (18301_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear apoptosis-inducing factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042503 GCST90234936 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein zwilch homolog level in Chronic kidney disease with hypertension and no diabetes (18302_204) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein zwilch in blood serum http://purl.obolibrary.org/obo/OBA_2044222 GCST90234937 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurogranin level in Chronic kidney disease with hypertension and no diabetes (18303_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurogranin in blood serum http://purl.obolibrary.org/obo/OBA_2042639 GCST90234938 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRCA2 and CDKN1A-interacting protein level in Chronic kidney disease with hypertension and no diabetes (18304_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRCA2 and CDKN1A-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2040785 GCST90234939 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paralemmin-1 level in Chronic kidney disease with hypertension and no diabetes (18306_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of paralemmin in blood serum http://purl.obolibrary.org/obo/OBA_2042752 GCST90234940 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inorganic pyrophosphatase 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18307_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inorganic pyrophosphatase 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042977 GCST90234941 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-binding protein 6 level in Chronic kidney disease with hypertension and no diabetes (18308_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of syntaxin-binding protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043720 GCST90234942 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Citrate synthase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18309_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of citrate synthase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041163 GCST90234943 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Selenoprotein W level in Chronic kidney disease with hypertension and no diabetes (18310_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of selenoprotein W in blood serum http://purl.obolibrary.org/obo/OBA_2043452 GCST90234944 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synapse-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (23409_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synapse-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043742 GCST90236389 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 3 subunit M level in Chronic kidney disease with hypertension and no diabetes (23410_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 3 subunit M in blood serum http://purl.obolibrary.org/obo/OBA_2041449 GCST90236390 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paraneoplastic antigen Ma2 level in Chronic kidney disease with hypertension and no diabetes (23411_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of paraneoplastic antigen Ma2 in blood serum http://purl.obolibrary.org/obo/OBA_2042951 GCST90236391 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 45 level in Chronic kidney disease with hypertension and no diabetes (23413_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 45 in blood serum http://purl.obolibrary.org/obo/OBA_2044626 GCST90236392 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-15 level in Chronic kidney disease with hypertension and no diabetes (23416_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-15 in blood serum http://purl.obolibrary.org/obo/OBA_2043585 GCST90236393 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 92 level in Chronic kidney disease with hypertension and no diabetes (23418_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 92 in blood serum http://purl.obolibrary.org/obo/OBA_2044264 GCST90236394 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (11716_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044786 GCST90233361 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte growth factor receptor level in Chronic kidney disease with hypertension and no diabetes (11814_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 hepatocyte growth factor receptor measurement http://www.ebi.ac.uk/efo/EFO_0008153 GCST90233362 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase JAK2 level in Chronic kidney disease with hypertension and no diabetes (11816_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase JAK2 measurement http://www.ebi.ac.uk/efo/EFO_0020825 GCST90233363 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosomal protein S6 kinase beta-1 level in Chronic kidney disease with hypertension and no diabetes (11817_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosomal protein S6 kinase beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040200 GCST90233364 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisome proliferator-activated receptor gamma coactivator 1-alpha level in Chronic kidney disease with hypertension and no diabetes (11825_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisome proliferator-activated receptor gamma coactivator 1-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042980 GCST90233365 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor ROR-gamma level in Chronic kidney disease with hypertension and no diabetes (11827_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor ROR-gamma in blood serum http://purl.obolibrary.org/obo/OBA_2040352 GCST90233366 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 11 level in Chronic kidney disease with hypertension and no diabetes (11830_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein phosphatase non-receptor type 11 measurement http://www.ebi.ac.uk/efo/EFO_0020835 GCST90233367 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frataxin, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (11833_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frataxin, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041637 GCST90233368 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epithelial discoidin domain-containing receptor 1 level in Chronic kidney disease with hypertension and no diabetes (11836_144) 466 African American individuals NA Illumina [14870897] (imputed) 0 epithelial discoidin domain-containing receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020362 GCST90233369 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 18 level in Chronic kidney disease with hypertension and no diabetes (11837_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020807 GCST90233370 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Piezo-type mechanosensitive ion channel component 1 level in Chronic kidney disease with hypertension and no diabetes (11838_130) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of piezo-type mechanosensitive ion channel component 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044446 GCST90233371 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Triggering receptor expressed on myeloid cells 2 level in Chronic kidney disease with hypertension and no diabetes (11851_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of triggering receptor expressed on myeloid cells 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043927 GCST90233372 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin gamma-B1 level in Chronic kidney disease with hypertension and no diabetes (11872_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin gamma-B1 in blood serum http://purl.obolibrary.org/obo/OBA_2042796 GCST90233373 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein DLX-4 level in Chronic kidney disease with hypertension and no diabetes (11910_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein DLX-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041319 GCST90233374 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 4B level in Chronic kidney disease with hypertension and no diabetes (11911_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233375 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrator complex subunit 3 level in Chronic kidney disease with hypertension and no diabetes (11934_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrator complex subunit 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042039 GCST90233376 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor level in Chronic kidney disease with hypertension and no diabetes (11949_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90233377 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily DCC subclass member 3 level in Chronic kidney disease with hypertension and no diabetes (11952_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233378 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (11955_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233379 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A2 level in Chronic kidney disease with hypertension and no diabetes (11969_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A2 in blood serum http://purl.obolibrary.org/obo/OBA_2043367 GCST90233380 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-type tyrosine-protein phosphatase H level in Chronic kidney disease with hypertension and no diabetes (11988_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-type tyrosine-protein phosphatase H in blood serum http://purl.obolibrary.org/obo/OBA_2043106 GCST90233381 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ER membrane protein complex subunit 1 level in Chronic kidney disease with hypertension and no diabetes (11989_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ER membrane protein complex subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044427 GCST90233382 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tight junction protein ZO-1 level in Chronic kidney disease with hypertension and no diabetes (12001_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tight junction protein ZO-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043861 GCST90233383 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell antigen CD7 level in Chronic kidney disease with hypertension and no diabetes (12008_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD7 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040334 GCST90233384 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 6-pyruvoyl tetrahydrobiopterin synthase level in Chronic kidney disease with hypertension and no diabetes (12014_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 6-pyruvoyl tetrahydrobiopterin synthase in blood serum http://purl.obolibrary.org/obo/OBA_2043113 GCST90233385 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 8 level in Chronic kidney disease with hypertension and no diabetes (18873_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040268 GCST90235034 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CCAAT/enhancer-binding protein alpha level in Chronic kidney disease with hypertension and no diabetes (18874_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CCAAT/enhancer-binding protein alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040982 GCST90235035 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chondrocalcin level in Chronic kidney disease with hypertension and no diabetes (18875_125) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of collagen type II alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040427 GCST90235036 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 4 level in Chronic kidney disease with hypertension and no diabetes (18876_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041025 GCST90235037 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calponin-2 level in Chronic kidney disease with hypertension and no diabetes (18877_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calponin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041067 GCST90235038 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gremlin-1 level in Chronic kidney disease with hypertension and no diabetes (18878_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 gremlin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020421 GCST90235039 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen Type III level in Chronic kidney disease with hypertension and no diabetes (18880_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(III) chain in blood serum http://purl.obolibrary.org/obo/OBA_2040436 GCST90235040 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dematin level in Chronic kidney disease with hypertension and no diabetes (23650_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dematin in blood serum http://purl.obolibrary.org/obo/OBA_2041487 GCST90236485 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal sarcosine oxidase level in Chronic kidney disease with hypertension and no diabetes (23652_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisomal sarcosine oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2042899 GCST90236486 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,3-mannosyltransferase ALG2 level in Chronic kidney disease with hypertension and no diabetes (23654_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,3/1,6-mannosyltransferase ALG2 in blood serum http://purl.obolibrary.org/obo/OBA_2040569 GCST90236487 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein L-like level in Chronic kidney disease with hypertension and no diabetes (23657_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein L-like in blood serum http://purl.obolibrary.org/obo/OBA_2041911 GCST90236488 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable asparagine--tRNA ligase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23658_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of asparagine--tRNA ligase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044495 GCST90236489 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Basic leucine zipper and W2 domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (23659_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eIF5-mimic protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040841 GCST90236490 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 41 level in Chronic kidney disease with hypertension and no diabetes (23660_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 41 in blood serum http://purl.obolibrary.org/obo/OBA_2042085 GCST90236491 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable Xaa-Pro aminopeptidase 3 level in Chronic kidney disease with hypertension and no diabetes (23661_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Xaa-Pro aminopeptidase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044570 GCST90236492 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar ATP synthase subunit C 1 level in Chronic kidney disease with hypertension and no diabetes (23663_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-type proton ATPase subunit C 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040733 GCST90236493 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S protease regulatory subunit 6A level in Chronic kidney disease with hypertension and no diabetes (23665_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 26S proteasome regulatory subunit 6A in blood serum http://purl.obolibrary.org/obo/OBA_2043074 GCST90236494 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional purine biosynthesis protein PURH level in Chronic kidney disease with hypertension and no diabetes (23666_35) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of bifunctional purine biosynthesis protein ATIC in blood serum http://purl.obolibrary.org/obo/OBA_2040722 GCST90236495 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2 level in Chronic kidney disease with hypertension and no diabetes (23669_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041706 GCST90236496 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2-(3-amino-3-carboxypropyl)histidine synthase subunit 2 level in Chronic kidney disease with hypertension and no diabetes (23670_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 2-(3-amino-3-carboxypropyl)histidine synthase subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041350 GCST90236497 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Spindly level in Chronic kidney disease with hypertension and no diabetes (23671_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Spindly in blood serum http://purl.obolibrary.org/obo/OBA_2044360 GCST90236498 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S proteasome non-ATPase regulatory subunit 6 level in Chronic kidney disease with hypertension and no diabetes (23672_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 26S proteasome non-ATPase regulatory subunit 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040397 GCST90236499 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23673_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lipoamide acyltransferase component of branched-chain alpha-keto acid dehydrogenase complex, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041236 GCST90236500 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centrosomal protein of 76 kDa level in Chronic kidney disease with hypertension and no diabetes (23675_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centrosomal protein of 76 kDa in blood serum http://purl.obolibrary.org/obo/OBA_2040987 GCST90236501 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NCK-interacting protein with SH3 domain level in Chronic kidney disease with hypertension and no diabetes (23677_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NCK-interacting protein with SH3 domain in blood serum http://purl.obolibrary.org/obo/OBA_2042528 GCST90236502 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-terminal Xaa-Pro-Lys N-methyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (12454_105) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methyltransferase-like protein 11A in blood serum http://purl.obolibrary.org/obo/OBA_2042345 GCST90233472 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myoneurin level in Chronic kidney disease with hypertension and no diabetes (12455_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myoneurin in blood serum http://purl.obolibrary.org/obo/OBA_2042486 GCST90233473 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 level in Chronic kidney disease with hypertension and no diabetes (12456_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042852 GCST90233474 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 1,2-dihydroxy-3-keto-5-methylthiopentene dioxygenase level in Chronic kidney disease with hypertension and no diabetes (12457_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of acireductone dioxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2040520 GCST90233475 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcineurin B homologous protein 1 level in Chronic kidney disease with hypertension and no diabetes (12458_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcineurin B homologous protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041015 GCST90233476 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family A member 1 level in Chronic kidney disease with hypertension and no diabetes (12459_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family A member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042926 GCST90233477 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-7 level in Chronic kidney disease with hypertension and no diabetes (12460_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of proteasome subunit alpha type-7 in blood serum http://purl.obolibrary.org/obo/OBA_2043066 GCST90233478 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD-dependent protein deacylase sirtuin-5, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12461_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NAD-dependent deacetylase sirtuin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043514 GCST90233479 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase SETMAR level in Chronic kidney disease with hypertension and no diabetes (12462_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone-lysine N-methyltransferase SETMAR in blood serum http://purl.obolibrary.org/obo/OBA_2043470 GCST90233480 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 13 level in Chronic kidney disease with hypertension and no diabetes (12463_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 13 in blood serum http://purl.obolibrary.org/obo/OBA_2042121 GCST90233481 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein A1 level in Chronic kidney disease with hypertension and no diabetes (12466_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041903 GCST90233482 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated protein RP/EB family member 1 level in Chronic kidney disease with hypertension and no diabetes (12469_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated protein RP/EB family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042296 GCST90233483 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Double-stranded RNA-binding protein Staufen homolog 1 level in Chronic kidney disease with hypertension and no diabetes (12471_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of double-stranded RNA-binding protein Staufen homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043696 GCST90233484 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD5 level in Chronic kidney disease with hypertension and no diabetes (12473_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD5 in blood serum http://purl.obolibrary.org/obo/OBA_2044319 GCST90233485 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chloride intracellular channel protein 5 level in Chronic kidney disease with hypertension and no diabetes (12475_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chloride intracellular channel protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041051 GCST90233486 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fructose-2,6-bisphosphatase TIGAR level in Chronic kidney disease with hypertension and no diabetes (12476_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fructose-2,6-bisphosphatase TIGAR in blood serum http://purl.obolibrary.org/obo/OBA_2044805 GCST90233487 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translin level in Chronic kidney disease with hypertension and no diabetes (12477_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of translin in blood serum http://purl.obolibrary.org/obo/OBA_2043949 GCST90233488 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S ribosomal protein L30 level in Chronic kidney disease with hypertension and no diabetes (12478_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S ribosomal protein L30 in blood serum http://purl.obolibrary.org/obo/OBA_2043321 GCST90233489 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-dependent protein kinase type I-beta regulatory subunit level in Chronic kidney disease with hypertension and no diabetes (12479_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-dependent protein kinase type I-beta regulatory subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043027 GCST90233490 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleosome-remodeling factor subunit BPTF level in Chronic kidney disease with hypertension and no diabetes (12482_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleosome-remodeling factor subunit BPTF in blood serum http://purl.obolibrary.org/obo/OBA_2040822 GCST90233491 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor ROR-beta level in Chronic kidney disease with hypertension and no diabetes (12483_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor ROR-beta in blood serum http://purl.obolibrary.org/obo/OBA_2043311 GCST90233492 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol transfer protein beta isoform level in Chronic kidney disease with hypertension and no diabetes (12484_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol transfer protein beta isoform in blood serum http://purl.obolibrary.org/obo/OBA_2042902 GCST90233493 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaredoxin-2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12486_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutaredoxin-2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041733 GCST90233494 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Malignant T-cell-amplified sequence 1 level in Chronic kidney disease with hypertension and no diabetes (12488_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of malignant T cell-amplified sequence 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042316 GCST90233495 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ragulator complex protein LAMTOR3 level in Chronic kidney disease with hypertension and no diabetes (12490_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase scaffold protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042295 GCST90233496 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tapasin level in Chronic kidney disease with hypertension and no diabetes (12378_71) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of tapasin in blood serum http://purl.obolibrary.org/obo/OBA_2043775 GCST90233422 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonyl reductase [NADPH] 1 level in Chronic kidney disease with hypertension and no diabetes (12381_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbonyl reductase [NADPH] 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040916 GCST90233423 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable ATP-dependent RNA helicase DDX58 level in Chronic kidney disease with hypertension and no diabetes (12382_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of antiviral innate immune response receptor RIG-I in blood serum http://purl.obolibrary.org/obo/OBA_2044278 GCST90233424 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COP9 signalosome complex subunit 7b level in Chronic kidney disease with hypertension and no diabetes (12384_92) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of COP9 signalosome complex subunit 7b in blood serum http://purl.obolibrary.org/obo/OBA_2041098 GCST90233425 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpain-3 level in Chronic kidney disease with hypertension and no diabetes (12385_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calpain-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040890 GCST90233426 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aminopeptidase B level in Chronic kidney disease with hypertension and no diabetes (12386_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of aminopeptidase B in blood serum http://purl.obolibrary.org/obo/OBA_2043303 GCST90233427 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ and LIM domain protein 4 level in Chronic kidney disease with hypertension and no diabetes (12387_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ and LIM domain protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044339 GCST90233428 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Origin recognition complex subunit 6 level in Chronic kidney disease with hypertension and no diabetes (12389_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of origin recognition complex subunit 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042710 GCST90233429 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ domain-containing protein 7 level in Chronic kidney disease with hypertension and no diabetes (12391_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ domain-containing protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044638 GCST90233430 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (12392_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040663 GCST90233431 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein C16orf54 level in Chronic kidney disease with hypertension and no diabetes (12394_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein C16orf54 in blood serum http://purl.obolibrary.org/obo/OBA_2044883 GCST90233432 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartate--tRNA ligase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12395_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aspartate--tRNA ligase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041232 GCST90233433 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-hydroxyisobutyryl-CoA hydrolase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12396_19) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 3-hydroxyisobutyryl-CoA hydrolase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041874 GCST90233434 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paired box protein Pax-4 level in Chronic kidney disease with hypertension and no diabetes (12398_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of paired box protein Pax-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042770 GCST90233435 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 T level in Chronic kidney disease with hypertension and no diabetes (12400_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 T in blood serum http://purl.obolibrary.org/obo/OBA_2044004 GCST90233436 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AMSH-like protease level in Chronic kidney disease with hypertension and no diabetes (12401_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AMSH-like protease in blood serum http://purl.obolibrary.org/obo/OBA_2043689 GCST90233437 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-39B level in Chronic kidney disease with hypertension and no diabetes (12403_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-39B in blood serum http://purl.obolibrary.org/obo/OBA_2043157 GCST90233438 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein Di-Ras3 level in Chronic kidney disease with hypertension and no diabetes (12406_119) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein Di-Ras3 in blood serum http://purl.obolibrary.org/obo/OBA_2041304 GCST90233439 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-22A level in Chronic kidney disease with hypertension and no diabetes (12408_333) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-22A in blood serum http://purl.obolibrary.org/obo/OBA_2043145 GCST90233440 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-7b level in Chronic kidney disease with hypertension and no diabetes (12409_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-7b in blood serum http://purl.obolibrary.org/obo/OBA_2043172 GCST90233441 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein max level in Chronic kidney disease with hypertension and no diabetes (12411_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein max in blood serum http://purl.obolibrary.org/obo/OBA_2042307 GCST90233442 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein beta/alpha level in Chronic kidney disease with hypertension and no diabetes (12414_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 14-3-3 protein beta/alpha measurement http://www.ebi.ac.uk/efo/EFO_0021957 GCST90233443 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelial differentiation-related factor 1 level in Chronic kidney disease with hypertension and no diabetes (12415_122) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endothelial differentiation-related factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041411 GCST90233444 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EKC/KEOPS complex subunit TPRKB level in Chronic kidney disease with hypertension and no diabetes (12417_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EKC/KEOPS complex subunit TPRKB in blood serum http://purl.obolibrary.org/obo/OBA_2043916 GCST90233445 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arachidonate 15-lipoxygenase B level in Chronic kidney disease with hypertension and no diabetes (12422_143) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyunsaturated fatty acid lipoxygenase ALOX15B in blood serum http://purl.obolibrary.org/obo/OBA_2040572 GCST90233446 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diphosphoinositol polyphosphate phosphohydrolase 3-beta level in Chronic kidney disease with hypertension and no diabetes (23623_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diphosphoinositol polyphosphate phosphohydrolase 3-beta in blood serum http://purl.obolibrary.org/obo/OBA_2042664 GCST90236470 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-secretase subunit PEN-2 level in Chronic kidney disease with hypertension and no diabetes (23624_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-secretase subunit PEN-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043054 GCST90236471 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein KIAA1143 level in Chronic kidney disease with hypertension and no diabetes (23625_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein KIAA1143 in blood serum http://purl.obolibrary.org/obo/OBA_2044853 GCST90236472 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0369 protein C6orf57 level in Chronic kidney disease with hypertension and no diabetes (23627_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of succinate dehydrogenase assembly factor 4, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044831 GCST90236473 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vimentin-type intermediate filament-associated coiled-coil protein level in Chronic kidney disease with hypertension and no diabetes (23629_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vimentin-type intermediate filament-associated coiled-coil protein in blood serum http://purl.obolibrary.org/obo/OBA_2044104 GCST90236474 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylgalactosamine kinase level in Chronic kidney disease with hypertension and no diabetes (23631_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of N-acetylgalactosamine kinase in blood serum http://purl.obolibrary.org/obo/OBA_2041657 GCST90236475 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Schlafen-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (23632_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Schlafen-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043543 GCST90236476 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF25 level in Chronic kidney disease with hypertension and no diabetes (23637_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RNF25 in blood serum http://purl.obolibrary.org/obo/OBA_2043296 GCST90236477 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carnosine N-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (23638_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carnosine N-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044885 GCST90236478 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable aminopeptidase NPEPL1 level in Chronic kidney disease with hypertension and no diabetes (23639_93) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable aminopeptidase NPEPL1 in blood serum http://purl.obolibrary.org/obo/OBA_2044454 GCST90236479 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EH domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (23640_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EH domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041433 GCST90236480 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydroxyacetone kinase level in Chronic kidney disease with hypertension and no diabetes (23644_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of triokinase/FMN cyclase in blood serum http://purl.obolibrary.org/obo/OBA_2041226 GCST90236481 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2-hydroxyacyl-CoA lyase 1 level in Chronic kidney disease with hypertension and no diabetes (23645_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of 2-hydroxyacyl-CoA lyase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041832 GCST90236482 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aryl-hydrocarbon-interacting protein-like 1 level in Chronic kidney disease with hypertension and no diabetes (23646_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aryl-hydrocarbon-interacting protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040544 GCST90236483 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (23649_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042123 GCST90236484 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tribbles homolog 2 level in Chronic kidney disease with hypertension and no diabetes (12363_70) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tribbles homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043932 GCST90233412 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RuvB-like 1 level in Chronic kidney disease with hypertension and no diabetes (12365_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RuvB-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043357 GCST90233413 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-crystallin D level in Chronic kidney disease with hypertension and no diabetes (12366_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-crystallin D in blood serum http://purl.obolibrary.org/obo/OBA_2041160 GCST90233414 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macoilin level in Chronic kidney disease with hypertension and no diabetes (12367_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of macoilin in blood serum http://purl.obolibrary.org/obo/OBA_2043874 GCST90233415 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone acetyltransferase KAT2B level in Chronic kidney disease with hypertension and no diabetes (12368_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone acetyltransferase KAT2B in blood serum http://purl.obolibrary.org/obo/OBA_2042776 GCST90233416 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein F level in Chronic kidney disease with hypertension and no diabetes (12370_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apolipoprotein F in blood serum http://purl.obolibrary.org/obo/OBA_2040628 GCST90233417 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomyosin alpha-3 chain level in Chronic kidney disease with hypertension and no diabetes (12372_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tropomyosin alpha-3 chain in blood serum http://purl.obolibrary.org/obo/OBA_2043911 GCST90233418 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transformer-2 protein homolog beta level in Chronic kidney disease with hypertension and no diabetes (12373_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transformer-2 protein homolog beta in blood serum http://purl.obolibrary.org/obo/OBA_2043478 GCST90233419 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-activating factor acetylhydrolase IB subunit gamma level in Chronic kidney disease with hypertension and no diabetes (12374_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of platelet-activating factor acetylhydrolase IB subunit alpha1 in blood serum http://purl.obolibrary.org/obo/OBA_2042745 GCST90233420 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 4 inhibitor D level in Chronic kidney disease with hypertension and no diabetes (12376_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 4 inhibitor D in blood serum http://purl.obolibrary.org/obo/OBA_2040972 GCST90233421 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chloride intracellular channel protein 4 level in Chronic kidney disease with hypertension and no diabetes (12491_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chloride intracellular channel protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041050 GCST90233497 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin thioesterase OTUB2 level in Chronic kidney disease with hypertension and no diabetes (12493_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin thioesterase OTUB2 in blood serum http://purl.obolibrary.org/obo/OBA_2042721 GCST90233498 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-aminobutyric acid receptor-associated protein-like 2 level in Chronic kidney disease with hypertension and no diabetes (12494_99) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-aminobutyric acid receptor-associated protein-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041649 GCST90233499 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tudor-interacting repair regulator protein level in Chronic kidney disease with hypertension and no diabetes (12497_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tudor-interacting repair regulator protein in blood serum http://purl.obolibrary.org/obo/OBA_2042668 GCST90233500 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tax1-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (12498_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Tax1-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043782 GCST90233501 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endophilin-A1 level in Chronic kidney disease with hypertension and no diabetes (12499_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endophilin-A1 in blood serum http://purl.obolibrary.org/obo/OBA_2043491 GCST90233502 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin-specific chaperone A level in Chronic kidney disease with hypertension and no diabetes (12501_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tubulin-specific chaperone A in blood serum http://purl.obolibrary.org/obo/OBA_2043789 GCST90233503 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ovarian cancer G-protein coupled receptor 1 level in Chronic kidney disease with hypertension and no diabetes (12503_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sphingosylphosphorylcholine receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040317 GCST90233504 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leiomodin-1 level in Chronic kidney disease with hypertension and no diabetes (12504_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leiomodin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042214 GCST90233505 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol-trisphosphate 3-kinase C level in Chronic kidney disease with hypertension and no diabetes (12507_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol-trisphosphate 3-kinase C in blood serum http://purl.obolibrary.org/obo/OBA_2042063 GCST90233506 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Charged multivesicular body protein 3 level in Chronic kidney disease with hypertension and no diabetes (12508_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of charged multivesicular body protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044106 GCST90233507 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein NDRG3 level in Chronic kidney disease with hypertension and no diabetes (18312_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein NDRG3 in blood serum http://purl.obolibrary.org/obo/OBA_2042537 GCST90234945 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isoaspartyl peptidase/L-asparaginase level in Chronic kidney disease with hypertension and no diabetes (18313_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of L-asparaginase in blood serum http://purl.obolibrary.org/obo/OBA_2040708 GCST90234946 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paired box protein Pax-8 level in Chronic kidney disease with hypertension and no diabetes (18314_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of paired box protein Pax-8 in blood serum http://purl.obolibrary.org/obo/OBA_2042771 GCST90234947 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-transporting protein 4 level in Chronic kidney disease with hypertension and no diabetes (18315_38) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of receptor-transporting protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043355 GCST90234948 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal-specific septin-3 level in Chronic kidney disease with hypertension and no diabetes (18316_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuronal-specific septin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043449 GCST90234949 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AN1-type zinc finger protein 5 level in Chronic kidney disease with hypertension and no diabetes (18317_111) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AN1-type zinc finger protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044180 GCST90234950 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endophilin-A3 level in Chronic kidney disease with hypertension and no diabetes (18318_98) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endophilin-A3 in blood serum http://purl.obolibrary.org/obo/OBA_2043492 GCST90234951 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyruvate dehydrogenase protein X component, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18319_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pyruvate dehydrogenase protein X component, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042827 GCST90234952 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18321_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042449 GCST90234953 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bifunctional arginine demethylase and lysyl-hydroxylase JMJD6 level in Chronic kidney disease with hypertension and no diabetes (18322_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional arginine demethylase and lysyl-hydroxylase JMJD6 in blood serum http://purl.obolibrary.org/obo/OBA_2042072 GCST90234954 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydropyrimidinase-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (18323_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydropyrimidinase-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041149 GCST90234955 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfite oxidase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18324_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfite oxidase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043736 GCST90234956 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 8 level in Chronic kidney disease with hypertension and no diabetes (18326_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen 8 in blood serum http://purl.obolibrary.org/obo/OBA_2042269 GCST90234957 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-5 level in Chronic kidney disease with hypertension and no diabetes (18327_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043590 GCST90234958 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyrroline-5-carboxylate reductase 2 level in Chronic kidney disease with hypertension and no diabetes (18328_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyrroline-5-carboxylate reductase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043124 GCST90234959 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribose-phosphate pyrophosphokinase 2 level in Chronic kidney disease with hypertension and no diabetes (18329_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribose-phosphate pyrophosphokinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043040 GCST90234960 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoglucomutase-2 level in Chronic kidney disease with hypertension and no diabetes (18330_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphopentomutase in blood serum http://purl.obolibrary.org/obo/OBA_2042865 GCST90234961 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucosylceramidase level in Chronic kidney disease with hypertension and no diabetes (18331_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lysosomal acid glucosylceramidase in blood serum http://purl.obolibrary.org/obo/OBA_2041678 GCST90234962 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complexin-1 level in Chronic kidney disease with hypertension and no diabetes (18332_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complexin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041117 GCST90234963 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytidine deaminase level in Chronic kidney disease with hypertension and no diabetes (18336_31) 466 African American individuals NA Illumina [14870897] (imputed) 2 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90234964 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDP-mannose 4,6 dehydratase level in Chronic kidney disease with hypertension and no diabetes (18337_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GDP-mannose 4,6 dehydratase in blood serum http://purl.obolibrary.org/obo/OBA_2041743 GCST90234965 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isocitrate dehydrogenase [NADP] cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (18338_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isocitrate dehydrogenase [NADP] cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2041969 GCST90234966 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-3 level in Chronic kidney disease with hypertension and no diabetes (18339_207) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit beta type-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043069 GCST90234967 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-4 level in Chronic kidney disease with hypertension and no diabetes (18340_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of proteasome subunit beta type-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040405 GCST90234968 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoserine aminotransferase level in Chronic kidney disease with hypertension and no diabetes (18342_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoserine aminotransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043052 GCST90234969 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal 2,4-dienoyl-CoA reductase level in Chronic kidney disease with hypertension and no diabetes (18343_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] in blood serum http://purl.obolibrary.org/obo/OBA_2041263 GCST90234970 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Laminin-2 level in Chronic kidney disease with hypertension and no diabetes (18347_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 laminin measurement http://www.ebi.ac.uk/efo/EFO_0020528 GCST90234971 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein D0 level in Chronic kidney disease with hypertension and no diabetes (18348_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein D0 in blood serum http://purl.obolibrary.org/obo/OBA_2041905 GCST90234972 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Radixin level in Chronic kidney disease with hypertension and no diabetes (18373_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of radixin in blood serum http://purl.obolibrary.org/obo/OBA_2040411 GCST90234973 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-36 receptor antagonist protein level in Chronic kidney disease with hypertension and no diabetes (18375_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-1 family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042006 GCST90234974 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin light chain 3 level in Chronic kidney disease with hypertension and no diabetes (18376_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin light chain 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040425 GCST90234975 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum albumin level in Chronic kidney disease with hypertension and no diabetes (18380_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 serum albumin measurement http://www.ebi.ac.uk/efo/EFO_0004535 GCST90234976 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldehyde dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (18381_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldehyde dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040562 GCST90234977 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catechol O-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (18382_109) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of catechol O-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041092 GCST90234978 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase FKBP3 level in Chronic kidney disease with hypertension and no diabetes (18383_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase FKBP3 in blood serum http://purl.obolibrary.org/obo/OBA_2041589 GCST90234979 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 26S proteasome non-ATPase regulatory subunit 10 level in Chronic kidney disease with hypertension and no diabetes (18385_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 26S proteasome non-ATPase regulatory subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043076 GCST90234980 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaredoxin-1 level in Chronic kidney disease with hypertension and no diabetes (18386_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutaredoxin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041732 GCST90234981 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hsc70-interacting protein level in Chronic kidney disease with hypertension and no diabetes (18387_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Hsc70-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2043670 GCST90234982 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-1/13 level in Chronic kidney disease with hypertension and no diabetes (18389_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-1/13 in blood serum http://purl.obolibrary.org/obo/OBA_2044315 GCST90234983 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. APOBEC1 complementation factor level in Chronic kidney disease with hypertension and no diabetes (12423_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of APOBEC1 complementation factor in blood serum http://purl.obolibrary.org/obo/OBA_2040449 GCST90233447 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thymocyte nuclear protein 1 level in Chronic kidney disease with hypertension and no diabetes (12424_107) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thymocyte nuclear protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043846 GCST90233448 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor 6 level in Chronic kidney disease with hypertension and no diabetes (12425_104) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040643 GCST90233449 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MOB kinase activator 1A level in Chronic kidney disease with hypertension and no diabetes (12426_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MOB kinase activator 1A in blood serum http://purl.obolibrary.org/obo/OBA_2042395 GCST90233450 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. M-phase inducer phosphatase 2 level in Chronic kidney disease with hypertension and no diabetes (12427_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of M-phase inducer phosphatase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040951 GCST90233451 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysophospholipase-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (12428_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysophospholipase-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042251 GCST90233452 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyadenylate-binding protein-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (12430_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyadenylate-binding protein-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042749 GCST90233453 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein pelota homolog level in Chronic kidney disease with hypertension and no diabetes (12431_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein pelota in blood serum http://purl.obolibrary.org/obo/OBA_2042845 GCST90233454 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcyclin-binding protein level in Chronic kidney disease with hypertension and no diabetes (12432_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcyclin-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2040871 GCST90233455 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 11 level in Chronic kidney disease with hypertension and no diabetes (12433_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2040664 GCST90233456 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IST1 homolog level in Chronic kidney disease with hypertension and no diabetes (12434_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of IST1 homolog in blood serum http://purl.obolibrary.org/obo/OBA_2044632 GCST90233457 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase omega-1 level in Chronic kidney disease with hypertension and no diabetes (12436_84) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutathione S-transferase omega-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041808 GCST90233458 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase ULK3 level in Chronic kidney disease with hypertension and no diabetes (12437_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase ULK3 in blood serum http://purl.obolibrary.org/obo/OBA_2044031 GCST90233459 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-3-methyladenine glycosylase level in Chronic kidney disease with hypertension and no diabetes (12438_127) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-3-methyladenine glycosylase in blood serum http://purl.obolibrary.org/obo/OBA_2042404 GCST90233460 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 9 level in Chronic kidney disease with hypertension and no diabetes (12439_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon regulatory factor 9 in blood serum http://purl.obolibrary.org/obo/OBA_2040380 GCST90233461 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-related GTP-binding protein RhoD level in Chronic kidney disease with hypertension and no diabetes (12442_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-related GTP-binding protein RhoD in blood serum http://purl.obolibrary.org/obo/OBA_2043266 GCST90233462 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor subfamily 5 group A member 2 level in Chronic kidney disease with hypertension and no diabetes (12444_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor subfamily 5 group A member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042633 GCST90233463 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 27 level in Chronic kidney disease with hypertension and no diabetes (12445_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 27 in blood serum http://purl.obolibrary.org/obo/OBA_2040593 GCST90233464 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase A1 level in Chronic kidney disease with hypertension and no diabetes (12446_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041802 GCST90233465 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycylpeptide N-tetradecanoyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (12448_246) 466 African American individuals NA Illumina [14870897] (imputed) 0 glycylpeptide n-tetradecanoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020413 GCST90233466 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase H level in Chronic kidney disease with hypertension and no diabetes (12449_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase H in blood serum http://purl.obolibrary.org/obo/OBA_2042987 GCST90233467 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphomevalonate kinase level in Chronic kidney disease with hypertension and no diabetes (12450_42) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of phosphomevalonate kinase in blood serum http://purl.obolibrary.org/obo/OBA_2042946 GCST90233468 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription regulator protein BACH1 level in Chronic kidney disease with hypertension and no diabetes (12451_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription regulator protein BACH1 in blood serum http://purl.obolibrary.org/obo/OBA_2040763 GCST90233469 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase SUV420H2 level in Chronic kidney disease with hypertension and no diabetes (12452_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone-lysine N-methyltransferase KMT5C in blood serum http://purl.obolibrary.org/obo/OBA_2043738 GCST90233470 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear RNA export factor 1 level in Chronic kidney disease with hypertension and no diabetes (12453_161) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear RNA export factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042681 GCST90233471 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase G level in Chronic kidney disease with hypertension and no diabetes (18449_33) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of peptidyl-prolyl cis-trans isomerase G in blood serum http://purl.obolibrary.org/obo/OBA_2042986 GCST90235009 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin E synthase 2 level in Chronic kidney disease with hypertension and no diabetes (18458_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostaglandin E synthase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043090 GCST90235010 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent RNA helicase DDX19A level in Chronic kidney disease with hypertension and no diabetes (18813_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent RNA helicase DDX19A in blood serum http://purl.obolibrary.org/obo/OBA_2041259 GCST90235011 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin beta A chain:Inhibin beta C chain heterodimer level in Chronic kidney disease with hypertension and no diabetes (18814_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 inhibin beta A chain:inhibin beta B chain heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020470 GCST90235012 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromobox protein homolog 1 level in Chronic kidney disease with hypertension and no diabetes (18817_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromobox protein homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040920 GCST90235013 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase C level in Chronic kidney disease with hypertension and no diabetes (18819_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of eukaryotic-type peptidyl-prolyl cis-trans isomerase C in blood serum http://purl.obolibrary.org/obo/OBA_2042985 GCST90235014 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C4a anaphylatoxin level in Chronic kidney disease with hypertension and no diabetes (18821_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235015 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H2B type 3-B level in Chronic kidney disease with hypertension and no diabetes (18823_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone H2B type 3-B in blood serum http://purl.obolibrary.org/obo/OBA_2041880 GCST90235016 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic initiation factor 4A-II level in Chronic kidney disease with hypertension and no diabetes (18824_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic initiation factor 4A-II in blood serum http://purl.obolibrary.org/obo/OBA_2041450 GCST90235017 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intelectin-1 level in Chronic kidney disease with hypertension and no diabetes (18830_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of intelectin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044678 GCST90235018 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeats and immunoglobulin-like domains protein 1 level in Chronic kidney disease with hypertension and no diabetes (18831_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leucine-rich repeats and immunoglobulin-like domains protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042226 GCST90235019 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum amyloid A-2 protein level in Chronic kidney disease with hypertension and no diabetes (18832_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of primate-type serum amyloid A-2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2044229 GCST90235020 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Astrocytic phosphoprotein PEA-15 level in Chronic kidney disease with hypertension and no diabetes (18833_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of astrocytic phosphoprotein PEA-15 in blood serum http://purl.obolibrary.org/obo/OBA_2042840 GCST90235021 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small glutamine-rich tetratricopeptide repeat-containing protein beta level in Chronic kidney disease with hypertension and no diabetes (18837_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small glutamine-rich tetratricopeptide repeat-containing protein beta in blood serum http://purl.obolibrary.org/obo/OBA_2043487 GCST90235022 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH2 domain-containing protein 1B level in Chronic kidney disease with hypertension and no diabetes (18840_205) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH2 domain-containing protein 1B in blood serum http://purl.obolibrary.org/obo/OBA_2043489 GCST90235023 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin B13 level in Chronic kidney disease with hypertension and no diabetes (18841_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin B13 in blood serum http://purl.obolibrary.org/obo/OBA_2043459 GCST90235024 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 D2 level in Chronic kidney disease with hypertension and no diabetes (18842_24) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ubiquitin-conjugating enzyme E2 D2 in blood serum http://purl.obolibrary.org/obo/OBA_2043992 GCST90235025 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4E-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (18859_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 4E-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041455 GCST90235026 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase kinase 1 level in Chronic kidney disease with hypertension and no diabetes (18860_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcium/calmodulin-dependent protein kinase kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020217 GCST90235027 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 2 level in Chronic kidney disease with hypertension and no diabetes (18863_176) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbohydrate sulfotransferase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020225 GCST90235028 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trypsin-3 level in Chronic kidney disease with hypertension and no diabetes (18864_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 trypsin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020791 GCST90235029 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcineurin subunit B type 2 level in Chronic kidney disease with hypertension and no diabetes (18866_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcineurin subunit B type 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043012 GCST90235030 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromobox protein homolog 3 level in Chronic kidney disease with hypertension and no diabetes (18868_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromobox protein homolog 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040922 GCST90235031 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD3 epsilon chain level in Chronic kidney disease with hypertension and no diabetes (18870_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD3 epsilon in blood serum http://purl.obolibrary.org/obo/OBA_2040229 GCST90235032 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Allograft inflammatory factor 1-like level in Chronic kidney disease with hypertension and no diabetes (18871_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of allograft inflammatory factor 1-like in blood serum http://purl.obolibrary.org/obo/OBA_2040541 GCST90235033 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionine adenosyltransferase 2 subunit beta level in Chronic kidney disease with hypertension and no diabetes (18392_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methionine adenosyltransferase 2 subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2042305 GCST90234984 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. [Protein ADP-ribosylarginine] hydrolase level in Chronic kidney disease with hypertension and no diabetes (18395_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ADP-ribosylhydrolase ARH1 in blood serum http://purl.obolibrary.org/obo/OBA_2040524 GCST90234985 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amino-terminal enhancer of split level in Chronic kidney disease with hypertension and no diabetes (18396_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TLE family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040528 GCST90234986 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldo-keto reductase family 1 member C4 level in Chronic kidney disease with hypertension and no diabetes (18397_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member C4 in blood serum http://purl.obolibrary.org/obo/OBA_2040552 GCST90234987 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-oxo-5-beta-steroid 4-dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (18398_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member D1 in blood serum http://purl.obolibrary.org/obo/OBA_2040553 GCST90234988 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A-kinase anchor protein 7 isoforms alpha and beta level in Chronic kidney disease with hypertension and no diabetes (18399_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of A-kinase anchor protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040744 GCST90234989 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA oxidative demethylase ALKBH2 level in Chronic kidney disease with hypertension and no diabetes (18400_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA oxidative demethylase ALKBH2 in blood serum http://purl.obolibrary.org/obo/OBA_2040570 GCST90234990 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 level in Chronic kidney disease with hypertension and no diabetes (18401_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-ketoglutarate-dependent dioxygenase alkB homolog 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040571 GCST90234991 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AMMECR1-like protein level in Chronic kidney disease with hypertension and no diabetes (18402_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AMMECR1-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2040580 GCST90234992 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AMP deaminase 2 level in Chronic kidney disease with hypertension and no diabetes (18403_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AMP deaminase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040582 GCST90234993 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 54 level in Chronic kidney disease with hypertension and no diabetes (18404_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 54 in blood serum http://purl.obolibrary.org/obo/OBA_2044238 GCST90234994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-1 complex subunit sigma-2 level in Chronic kidney disease with hypertension and no diabetes (18405_117) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-1 complex subunit sigma-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040610 GCST90234995 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 2-binding protein level in Chronic kidney disease with hypertension and no diabetes (18407_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 2-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2040667 GCST90234996 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor 4 level in Chronic kidney disease with hypertension and no diabetes (18408_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040641 GCST90234997 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor 5 level in Chronic kidney disease with hypertension and no diabetes (18409_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040642 GCST90234998 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 15 level in Chronic kidney disease with hypertension and no diabetes (18411_83) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ADP-ribosylation factor-like protein 15 in blood serum http://purl.obolibrary.org/obo/OBA_2040665 GCST90234999 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 4D level in Chronic kidney disease with hypertension and no diabetes (18413_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 4D in blood serum http://purl.obolibrary.org/obo/OBA_2040669 GCST90235000 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 5A level in Chronic kidney disease with hypertension and no diabetes (18414_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 5A in blood serum http://purl.obolibrary.org/obo/OBA_2040670 GCST90235001 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 6 level in Chronic kidney disease with hypertension and no diabetes (18415_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040672 GCST90235002 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 9 level in Chronic kidney disease with hypertension and no diabetes (18416_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2040677 GCST90235003 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arsenite methyltransferase level in Chronic kidney disease with hypertension and no diabetes (18417_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arsenite methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2040687 GCST90235004 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Actin-related protein 2/3 complex subunit 5 level in Chronic kidney disease with hypertension and no diabetes (18419_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin-related protein 2/3 complex subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040683 GCST90235005 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diphosphomevalonate decarboxylase level in Chronic kidney disease with hypertension and no diabetes (18422_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diphosphomevalonate decarboxylase in blood serum http://purl.obolibrary.org/obo/OBA_2042467 GCST90235006 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TATA box-binding protein-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (18434_141) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TATA box-binding protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043795 GCST90235007 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UBX domain-containing protein 2B level in Chronic kidney disease with hypertension and no diabetes (18435_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UBX domain-containing protein 2B in blood serum http://purl.obolibrary.org/obo/OBA_2044015 GCST90235008 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor SOX-10 level in Chronic kidney disease with hypertension and no diabetes (23678_132) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor SOX-10 in blood serum http://purl.obolibrary.org/obo/OBA_2043601 GCST90236503 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sister chromatid cohesion protein DCC1 level in Chronic kidney disease with hypertension and no diabetes (23679_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sister chromatid cohesion protein DCC1 in blood serum http://purl.obolibrary.org/obo/OBA_2041367 GCST90236504 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MCP-1 Induced Protein level in Chronic kidney disease with hypertension and no diabetes (23680_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoribonuclease ZC3H12A in blood serum http://purl.obolibrary.org/obo/OBA_2044175 GCST90236505 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small RNA 2'-O-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (23682_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small RNA 2'-O-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044413 GCST90236506 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tripartite motif-containing protein 55 level in Chronic kidney disease with hypertension and no diabetes (23683_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tripartite motif-containing protein 55 in blood serum http://purl.obolibrary.org/obo/OBA_2043937 GCST90236507 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Meiosis 1 arrest protein level in Chronic kidney disease with hypertension and no diabetes (23685_132) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of meiosis 1 arrest protein in blood serum http://purl.obolibrary.org/obo/OBA_2044850 GCST90236508 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CWF19-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (23686_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CWF19-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041204 GCST90236509 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TBC1 domain family member 20 level in Chronic kidney disease with hypertension and no diabetes (23687_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TBC1 domain family member 20 in blood serum http://purl.obolibrary.org/obo/OBA_2043784 GCST90236510 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Copine-6 level in Chronic kidney disease with hypertension and no diabetes (23689_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of copine-6 in blood serum http://purl.obolibrary.org/obo/OBA_2041123 GCST90236511 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein 41 level in Chronic kidney disease with hypertension and no diabetes (23690_228) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein 41 in blood serum http://purl.obolibrary.org/obo/OBA_2043208 GCST90236512 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin--tyrosine ligase-like protein 12 level in Chronic kidney disease with hypertension and no diabetes (23691_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin--tyrosine ligase-like protein 12 in blood serum http://purl.obolibrary.org/obo/OBA_2043957 GCST90236513 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAP kinase-interacting serine/threonine-protein kinase 1 level in Chronic kidney disease with hypertension and no diabetes (23693_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MAP kinase-interacting serine/threonine-protein kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042373 GCST90236514 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibronectin type III and SPRY domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (23695_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibronectin type III and SPRY domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041620 GCST90236515 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA (adenine(58)-N(1))-methyltransferase non-catalytic subunit TRM6 level in Chronic kidney disease with hypertension and no diabetes (23696_256) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA (adenine-N(1)-)-methyltransferase non-catalytic subunit TRM6 in blood serum http://purl.obolibrary.org/obo/OBA_2043941 GCST90236516 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23699_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydrolipoyllysine-residue succinyltransferase component of 2-oxoglutarate dehydrogenase complex, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041316 GCST90236517 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-binding cassette sub-family F member 3 level in Chronic kidney disease with hypertension and no diabetes (23700_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-binding cassette sub-family F member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044249 GCST90236518 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3KBP1-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (23702_98) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH3KBP1-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043502 GCST90236519 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ and LIM domain protein 5 level in Chronic kidney disease with hypertension and no diabetes (23703_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ and LIM domain protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042835 GCST90236520 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 24 level in Chronic kidney disease with hypertension and no diabetes (23704_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipid transfer protein C2CD2L in blood serum http://purl.obolibrary.org/obo/OBA_2044692 GCST90236521 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CTP synthase 1 level in Chronic kidney disease with hypertension and no diabetes (23705_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CTP synthase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041190 GCST90236522 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA (adenine(58)-N(1))-methyltransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23706_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of potential tRNA (adenine-N(1)-)-methyltransferase catalytic subunit TRMT61B in blood serum http://purl.obolibrary.org/obo/OBA_2043942 GCST90236523 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0705 protein C11orf49 level in Chronic kidney disease with hypertension and no diabetes (23767_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centriolar satellite-associated tubulin polyglutamylase complex regulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044874 GCST90236524 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic AMP-dependent transcription factor ATF-5 level in Chronic kidney disease with hypertension and no diabetes (23771_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic AMP-dependent transcription factor ATF-5 in blood serum http://purl.obolibrary.org/obo/OBA_2040714 GCST90236525 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM110A level in Chronic kidney disease with hypertension and no diabetes (23783_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM110A in blood serum http://purl.obolibrary.org/obo/OBA_2044492 GCST90236526 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C5 level in Chronic kidney disease with hypertension and no diabetes (2381_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C5 measurement http://www.ebi.ac.uk/efo/EFO_0020278 GCST90236527 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Voltage-dependent L-type calcium channel subunit beta-3 level in Chronic kidney disease with hypertension and no diabetes (24237_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-dependent L-type calcium channel subunit beta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040869 GCST90236553 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab-interacting lysosomal protein level in Chronic kidney disease with hypertension and no diabetes (24244_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab-interacting lysosomal protein in blood serum http://purl.obolibrary.org/obo/OBA_2043273 GCST90236554 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin light chain 3 level in Chronic kidney disease with hypertension and no diabetes (24245_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kinesin light chain 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042117 GCST90236555 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0235 protein C15orf40 level in Chronic kidney disease with hypertension and no diabetes (24247_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UPF0235 protein C15orf40 in blood serum http://purl.obolibrary.org/obo/OBA_2044852 GCST90236556 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable peptide chain release factor C12orf65, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (24252_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial translation release factor in rescue in blood serum http://purl.obolibrary.org/obo/OBA_2044872 GCST90236557 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic peptide chain release factor GTP-binding subunit ERF3B level in Chronic kidney disease with hypertension and no diabetes (24253_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic peptide chain release factor GTP-binding subunit ERF3B in blood serum http://purl.obolibrary.org/obo/OBA_2041799 GCST90236558 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epsin-1 level in Chronic kidney disease with hypertension and no diabetes (24255_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epsin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041496 GCST90236559 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 40 level in Chronic kidney disease with hypertension and no diabetes (24256_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 40 in blood serum http://purl.obolibrary.org/obo/OBA_2044710 GCST90236560 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein P4 level in Chronic kidney disease with hypertension and no diabetes (24259_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein P4 in blood serum http://purl.obolibrary.org/obo/OBA_2041614 GCST90236561 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase setd3 level in Chronic kidney disease with hypertension and no diabetes (24260_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin-histidine N-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044745 GCST90236562 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Death-associated protein kinase 3 level in Chronic kidney disease with hypertension and no diabetes (24261_202) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of death-associated protein kinase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041230 GCST90236563 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Occludin level in Chronic kidney disease with hypertension and no diabetes (24263_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of occludin in blood serum http://purl.obolibrary.org/obo/OBA_2040403 GCST90236564 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAGUK p55 subfamily member 2 level in Chronic kidney disease with hypertension and no diabetes (24265_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MAGUK p55 subfamily member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044243 GCST90236565 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myocyte-specific enhancer factor 2D level in Chronic kidney disease with hypertension and no diabetes (24266_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of myocyte-specific enhancer factor 2D in blood serum http://purl.obolibrary.org/obo/OBA_2042331 GCST90236566 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PWWP domain-containing protein 2B level in Chronic kidney disease with hypertension and no diabetes (24267_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PWWP domain-containing protein 2B in blood serum http://purl.obolibrary.org/obo/OBA_2044348 GCST90236567 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRB2-associated-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (24268_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GRB2-associated-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041646 GCST90236568 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (24273_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thioredoxin domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043968 GCST90236569 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 25 level in Chronic kidney disease with hypertension and no diabetes (24276_171) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of outer dynein arm-docking complex subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044375 GCST90236570 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Copine-7 level in Chronic kidney disease with hypertension and no diabetes (24277_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of copine-7 in blood serum http://purl.obolibrary.org/obo/OBA_2041124 GCST90236571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 3 level in Chronic kidney disease with hypertension and no diabetes (24278_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044063 GCST90236572 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U3 small nucleolar RNA-associated protein 6 homolog level in Chronic kidney disease with hypertension and no diabetes (24279_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U3 small nucleolar RNA-associated protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2044070 GCST90236573 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Meiosis expressed gene 1 protein homolog level in Chronic kidney disease with hypertension and no diabetes (24286_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of meiosis expressed gene 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042333 GCST90236574 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing transmembrane protein C7orf53 level in Chronic kidney disease with hypertension and no diabetes (24289_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich single-pass membrane protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044843 GCST90236575 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C20orf202 level in Chronic kidney disease with hypertension and no diabetes (24290_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C20orf202 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044891 GCST90236576 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nonspecific lipid-transfer protein level in Chronic kidney disease with hypertension and no diabetes (24293_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90236577 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctional adhesion molecule-like level in Chronic kidney disease with hypertension and no diabetes (8232_90) 466 African American individuals NA Illumina [14870897] (imputed) 1 junctional adhesion molecule-like measurement http://www.ebi.ac.uk/efo/EFO_0020511 GCST90238834 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inter-alpha-trypsin inhibitor heavy chain H5 level in Chronic kidney disease with hypertension and no diabetes (8233_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inter-alpha-trypsin inhibitor heavy chain H5 in blood serum http://purl.obolibrary.org/obo/OBA_2042059 GCST90238835 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretogranin-1 level in Chronic kidney disease with hypertension and no diabetes (8235_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretogranin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041004 GCST90238836 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0729 protein C18orf32 level in Chronic kidney disease with hypertension and no diabetes (8236_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UPF0729 protein C18orf32 in blood serum http://purl.obolibrary.org/obo/OBA_2044851 GCST90238837 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sclerostin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8237_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sclerostin domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043600 GCST90238838 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cholinesterase level in Chronic kidney disease with hypertension and no diabetes (8239_223) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cholinesterase in blood serum http://purl.obolibrary.org/obo/OBA_2040786 GCST90238839 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane glycoprotein NMB level in Chronic kidney disease with hypertension and no diabetes (8240_207) 466 African American individuals NA Illumina [14870897] (imputed) 0 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90238840 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 2 member L level in Chronic kidney disease with hypertension and no diabetes (8242_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 2 member L in blood serum http://purl.obolibrary.org/obo/OBA_2044744 GCST90238841 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 1 level in Chronic kidney disease with hypertension and no diabetes (8243_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine protease inhibitor Kazal-type 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043629 GCST90238842 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-(1,6)-fucosyltransferase level in Chronic kidney disease with hypertension and no diabetes (8244_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of alpha-(1,6)-fucosyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041635 GCST90238843 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 5 level in Chronic kidney disease with hypertension and no diabetes (8245_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90238844 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proprotein convertase subtilisin/kexin type 9 level in Chronic kidney disease with hypertension and no diabetes (8246_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90238845 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 14 level in Chronic kidney disease with hypertension and no diabetes (8248_222) 466 African American individuals NA Illumina [14870897] (imputed) 0 sialic acid-binding Ig-like lectin 14 measurement http://www.ebi.ac.uk/efo/EFO_0008284 GCST90238846 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ALK tyrosine kinase receptor level in Chronic kidney disease with hypertension and no diabetes (8249_124) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ALK tyrosine kinase receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040255 GCST90238847 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-type tyrosine-protein phosphatase eta level in Chronic kidney disease with hypertension and no diabetes (8250_2) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of receptor-type tyrosine-protein phosphatase eta in blood serum http://purl.obolibrary.org/obo/OBA_2040357 GCST90238848 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Palmitoleoyl-protein carboxylesterase NOTUM level in Chronic kidney disease with hypertension and no diabetes (8252_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein notum in blood serum http://purl.obolibrary.org/obo/OBA_2042609 GCST90238849 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (8253_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042973 GCST90238850 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein MRVI1 level in Chronic kidney disease with hypertension and no diabetes (8255_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol 1,4,5-triphosphate receptor associated 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042437 GCST90238851 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxytocin-neurophysin 1 level in Chronic kidney disease with hypertension and no diabetes (8257_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxytocin-neurophysin 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042729 GCST90238852 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-glucuronic acid decarboxylase 1 level in Chronic kidney disease with hypertension and no diabetes (8258_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UDP-glucuronic acid decarboxylase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044073 GCST90238853 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Erythrocyte band 7 integral membrane protein level in Chronic kidney disease with hypertension and no diabetes (8261_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stomatin in blood serum http://purl.obolibrary.org/obo/OBA_2043705 GCST90238854 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein D level in Chronic kidney disease with hypertension and no diabetes (8262_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 apolipoprotein D measurement http://www.ebi.ac.uk/efo/EFO_0020156 GCST90238855 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (8264_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90238856 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lamina-associated polypeptide 2, isoforms beta/gamma level in Chronic kidney disease with hypertension and no diabetes (8265_225) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lamina-associated polypeptide 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044324 GCST90238857 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan sulfate glucosamine 3-O-sulfotransferase 3A1 level in Chronic kidney disease with hypertension and no diabetes (8268_98) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heparan sulfate glucosamine 3-O-sulfotransferase 3A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041931 GCST90238858 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartate aminotransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (23903_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aspartate aminotransferase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041767 GCST90236528 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-7 level in Chronic kidney disease with hypertension and no diabetes (23915_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-7a in blood serum http://purl.obolibrary.org/obo/OBA_2043171 GCST90236529 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1F level in Chronic kidney disease with hypertension and no diabetes (23923_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1F in blood serum http://purl.obolibrary.org/obo/OBA_2042994 GCST90236530 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proline-rich transmembrane protein 2 level in Chronic kidney disease with hypertension and no diabetes (23929_159) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proline-rich transmembrane protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044347 GCST90236531 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PAXIP1-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (23967_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of PAXIP1-associated glutamate-rich protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042733 GCST90236532 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase A1 level in Chronic kidney disease with hypertension and no diabetes (23981_172) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041112 GCST90236533 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and immunoglobulin domain-containing protein 10-like level in Chronic kidney disease with hypertension and no diabetes (24011_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-set and immunoglobulin domain-containing protein 10-like in blood serum http://purl.obolibrary.org/obo/OBA_2044561 GCST90236534 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metabotropic glutamate receptor 4 level in Chronic kidney disease with hypertension and no diabetes (24013_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of metabotropic glutamate receptor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041794 GCST90236535 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. soluble Endothelial protein C receptor level in Chronic kidney disease with hypertension and no diabetes (24023_35) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of endothelial protein C receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040274 GCST90236536 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon epsilon-1 level in Chronic kidney disease with hypertension and no diabetes (24027_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon epsilon in blood serum http://purl.obolibrary.org/obo/OBA_2041984 GCST90236537 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycogen synthase kinase-3 beta level in Chronic kidney disease with hypertension and no diabetes (24050_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycogen synthase kinase-3 beta in blood serum http://purl.obolibrary.org/obo/OBA_2041797 GCST90236538 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cleavage stimulation factor 50 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (24055_44) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cleavage stimulation factor subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041177 GCST90236539 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elongation factor 1-gamma level in Chronic kidney disease with hypertension and no diabetes (24111_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of elongation factor 1-gamma in blood serum http://purl.obolibrary.org/obo/OBA_2041421 GCST90236540 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphotriesterase-related protein level in Chronic kidney disease with hypertension and no diabetes (24179_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphotriesterase-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2043087 GCST90236541 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G antigen family C member 1 level in Chronic kidney disease with hypertension and no diabetes (24201_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of P antigen family member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042747 GCST90236542 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxymethylglutaryl-CoA lyase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (24211_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hydroxymethylglutaryl-CoA lyase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041891 GCST90236543 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paired mesoderm homeobox protein 1 level in Chronic kidney disease with hypertension and no diabetes (24215_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of paired mesoderm homeobox protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043046 GCST90236544 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mth938 domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (24216_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Mth938 domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2044875 GCST90236545 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calgranulin A level in Chronic kidney disease with hypertension and no diabetes (24217_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-A8 in blood serum http://purl.obolibrary.org/obo/OBA_2043369 GCST90236546 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisome proliferator activated receptor gamma level in Chronic kidney disease with hypertension and no diabetes (24221_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisome proliferator-activated receptor gamma in blood serum http://purl.obolibrary.org/obo/OBA_2042979 GCST90236547 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Negative elongation factor A level in Chronic kidney disease with hypertension and no diabetes (24222_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of negative elongation factor A in blood serum http://purl.obolibrary.org/obo/OBA_2044135 GCST90236548 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase theta-2 level in Chronic kidney disease with hypertension and no diabetes (24223_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase theta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041810 GCST90236549 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fascin level in Chronic kidney disease with hypertension and no diabetes (24226_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fascin in blood serum http://purl.obolibrary.org/obo/OBA_2041619 GCST90236550 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EH domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (24235_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EH domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041432 GCST90236551 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptic vesicle membrane protein VAT-1 homolog-like level in Chronic kidney disease with hypertension and no diabetes (24236_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptic vesicle membrane protein VAT-1-like in blood serum http://purl.obolibrary.org/obo/OBA_2044085 GCST90236552 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostate-associated microseminoprotein level in Chronic kidney disease with hypertension and no diabetes (8080_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostate-associated microseminoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2042441 GCST90238809 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive phospholipase D5 level in Chronic kidney disease with hypertension and no diabetes (8081_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inactive phospholipase D5 in blood serum http://purl.obolibrary.org/obo/OBA_2042923 GCST90238810 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integral membrane protein 2B level in Chronic kidney disease with hypertension and no diabetes (8086_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integral membrane protein 2B in blood serum http://purl.obolibrary.org/obo/OBA_2044704 GCST90238811 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF13 level in Chronic kidney disease with hypertension and no diabetes (8087_250) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RNF13 in blood serum http://purl.obolibrary.org/obo/OBA_2043290 GCST90238812 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Type III endosome membrane protein TEMP level in Chronic kidney disease with hypertension and no diabetes (8088_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of type III endosome membrane protein TEMP in blood serum http://purl.obolibrary.org/obo/OBA_2044889 GCST90238813 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor subfamily 4 group A member 1 level in Chronic kidney disease with hypertension and no diabetes (8089_173) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor subfamily 4 group A member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042632 GCST90238814 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mannan-binding lectin serine protease 1 level in Chronic kidney disease with hypertension and no diabetes (8091_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90238815 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-6 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (8092_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of interleukin-6 receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040293 GCST90238816 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized family 31 glucosidase KIAA1161 level in Chronic kidney disease with hypertension and no diabetes (8093_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238817 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CDGSH iron-sulfur domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (8094_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CDGSH iron-sulfur domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041035 GCST90238818 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase F, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8095_213) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptidyl-prolyl cis-trans isomerase F, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020627 GCST90238819 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lipase member N level in Chronic kidney disease with hypertension and no diabetes (8097_77) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lipase member N in blood serum http://purl.obolibrary.org/obo/OBA_2042209 GCST90238820 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thromboxane-A synthase level in Chronic kidney disease with hypertension and no diabetes (8098_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thromboxane-A synthase in blood serum http://purl.obolibrary.org/obo/OBA_2043799 GCST90238821 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spondin-2 level in Chronic kidney disease with hypertension and no diabetes (8099_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spondin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043641 GCST90238822 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADM2 level in Chronic kidney disease with hypertension and no diabetes (8100_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein ADM2 in blood serum http://purl.obolibrary.org/obo/OBA_2040522 GCST90238823 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C1orf186 level in Chronic kidney disease with hypertension and no diabetes (8102_239) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of hemoglobinization and erythroid cell expansion protein (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044910 GCST90238824 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-10 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (8104_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-10 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0021890 GCST90238825 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translocon-associated protein subunit alpha level in Chronic kidney disease with hypertension and no diabetes (8106_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of translocon-associated protein subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043666 GCST90238826 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 234 level in Chronic kidney disease with hypertension and no diabetes (8107_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 234 in blood serum http://purl.obolibrary.org/obo/OBA_2044687 GCST90238827 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zymogen granule membrane protein 16 level in Chronic kidney disease with hypertension and no diabetes (8219_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of zymogen granule membrane protein 16 in blood serum http://purl.obolibrary.org/obo/OBA_2044183 GCST90238828 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C10orf35 level in Chronic kidney disease with hypertension and no diabetes (8220_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM241B in blood serum http://purl.obolibrary.org/obo/OBA_2044854 GCST90238829 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage migration inhibitory factor level in Chronic kidney disease with hypertension and no diabetes (8221_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST90238830 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-related family member 3 level in Chronic kidney disease with hypertension and no diabetes (8222_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-related family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040962 GCST90238831 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-B receptor 2 level in Chronic kidney disease with hypertension and no diabetes (8225_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90238832 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucoside xylosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (8229_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glucoside xylosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044403 GCST90238833 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromosome transmission fidelity protein 8 homolog level in Chronic kidney disease with hypertension and no diabetes (24294_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromosome transmission fidelity protein 8 homolog in blood serum http://purl.obolibrary.org/obo/OBA_2044383 GCST90236578 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 16 level in Chronic kidney disease with hypertension and no diabetes (24299_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 16 in blood serum http://purl.obolibrary.org/obo/OBA_2040976 GCST90236579 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component C8 level in Chronic kidney disease with hypertension and no diabetes (2429_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement component C8 measurement http://www.ebi.ac.uk/efo/EFO_0008094 GCST90236580 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipase A2 level in Chronic kidney disease with hypertension and no diabetes (4910_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipase A2 in blood serum http://purl.obolibrary.org/obo/OBA_2042913 GCST90237742 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase P level in Chronic kidney disease with hypertension and no diabetes (4911_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 glutathione s-transferase p measurement http://www.ebi.ac.uk/efo/EFO_0020410 GCST90237743 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartate aminotransferase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (4912_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 aspartate aminotransferase, cytoplasmic measurement http://www.ebi.ac.uk/efo/EFO_0008031 GCST90237744 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 16 level in Chronic kidney disease with hypertension and no diabetes (4913_78) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0008044 GCST90237745 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Human Chorionic Gonadotropin level in Chronic kidney disease with hypertension and no diabetes (4914_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 human Chorionic Gonadotropin measurement http://www.ebi.ac.uk/efo/EFO_0008156 GCST90237746 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin D level in Chronic kidney disease with hypertension and no diabetes (4916_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 immunoglobulin D measurement http://www.ebi.ac.uk/efo/EFO_0020463 GCST90237747 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-V: beta-5 complex level in Chronic kidney disease with hypertension and no diabetes (4917_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-V: beta-5 complex measurement http://www.ebi.ac.uk/efo/EFO_0020480 GCST90237748 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kininogen-1 level in Chronic kidney disease with hypertension and no diabetes (4918_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 kininogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008198 GCST90237749 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysozyme C level in Chronic kidney disease with hypertension and no diabetes (4920_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 lysozyme C measurement http://www.ebi.ac.uk/efo/EFO_0008216 GCST90237750 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 19 level in Chronic kidney disease with hypertension and no diabetes (4922_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 19 measurement http://www.ebi.ac.uk/efo/EFO_0008047 GCST90237751 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Muellerian-inhibiting factor level in Chronic kidney disease with hypertension and no diabetes (4923_79) 466 African American individuals NA Illumina [14870897] (imputed) 2 muellerian-inhibiting factor measurement http://www.ebi.ac.uk/efo/EFO_0020584 GCST90237752 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagenase 3 level in Chronic kidney disease with hypertension and no diabetes (4925_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 collagenase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020271 GCST90237753 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sex hormone-binding globulin level in Chronic kidney disease with hypertension and no diabetes (4929_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90237754 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stanniocalcin-1 level in Chronic kidney disease with hypertension and no diabetes (4930_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 stanniocalcin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020753 GCST90237755 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tissue Factor level in Chronic kidney disease with hypertension and no diabetes (4931_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 tissue factor measurement http://www.ebi.ac.uk/efo/EFO_0010623 GCST90237756 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epiregulin level in Chronic kidney disease with hypertension and no diabetes (4956_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 epiregulin measurement http://www.ebi.ac.uk/efo/EFO_0020361 GCST90237757 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anterior gradient protein 2 homolog level in Chronic kidney disease with hypertension and no diabetes (4959_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 anterior gradient protein 2 homolog measurement http://www.ebi.ac.uk/efo/EFO_0020152 GCST90237758 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Annexin A1 level in Chronic kidney disease with hypertension and no diabetes (4960_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 annexin A1 measurement http://www.ebi.ac.uk/efo/EFO_0008026 GCST90237759 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cerebral dopamine neurotrophic factor level in Chronic kidney disease with hypertension and no diabetes (4962_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 cerebral dopamine neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0020254 GCST90237760 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-regulated phosphoprotein 19 level in Chronic kidney disease with hypertension and no diabetes (4963_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 cAMP-regulated phosphoprotein 19 measurement http://www.ebi.ac.uk/efo/EFO_0020223 GCST90237761 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum aminopeptidase 1 level in Chronic kidney disease with hypertension and no diabetes (4964_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 endoplasmic reticulum aminopeptidase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008119 GCST90237762 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement component 1 Q subcomponent-binding protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (4967_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement component 1 q subcomponent-binding protein, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020280 GCST90237763 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage-capping protein level in Chronic kidney disease with hypertension and no diabetes (4968_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage-capping protein measurement http://www.ebi.ac.uk/efo/EFO_0020549 GCST90237764 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 1 level in Chronic kidney disease with hypertension and no diabetes (4969_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020227 GCST90237765 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 2 level in Chronic kidney disease with hypertension and no diabetes (4970_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 carbonic anhydrase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020228 GCST90237766 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin Z level in Chronic kidney disease with hypertension and no diabetes (4971_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin Z measurement http://www.ebi.ac.uk/efo/EFO_0008074 GCST90237767 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Baculoviral IAP repeat-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (4973_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 baculoviral IAP repeat-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020173 GCST90237768 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adapter molecule crk level in Chronic kidney disease with hypertension and no diabetes (4976_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 adapter molecule CRK measurement http://www.ebi.ac.uk/efo/EFO_0020128 GCST90237769 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Drebrin-like protein level in Chronic kidney disease with hypertension and no diabetes (4978_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 drebrin-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020333 GCST90237770 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dermatopontin level in Chronic kidney disease with hypertension and no diabetes (4979_34) 466 African American individuals NA Illumina [14870897] (imputed) 1 dermatopontin measurement http://www.ebi.ac.uk/efo/EFO_0008108 GCST90237771 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmocollin-3 level in Chronic kidney disease with hypertension and no diabetes (4981_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 desmocollin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020320 GCST90237772 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elafin level in Chronic kidney disease with hypertension and no diabetes (4982_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 elafin measurement http://www.ebi.ac.uk/efo/EFO_0008117 GCST90237773 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum resident protein 29 level in Chronic kidney disease with hypertension and no diabetes (4983_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 endoplasmic reticulum resident protein 29 measurement http://www.ebi.ac.uk/efo/EFO_0020346 GCST90237774 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-formylglutathione hydrolase level in Chronic kidney disease with hypertension and no diabetes (4984_83) 466 African American individuals NA Illumina [14870897] (imputed) 1 S-formylglutathione hydrolase measurement http://www.ebi.ac.uk/efo/EFO_0008275 GCST90237775 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein, epidermal level in Chronic kidney disease with hypertension and no diabetes (4985_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 fatty acid-binding protein, epidermal measurement http://www.ebi.ac.uk/efo/EFO_0020372 GCST90237776 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Focal adhesion kinase 1 level in Chronic kidney disease with hypertension and no diabetes (4986_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 focal adhesion kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020393 GCST90237777 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin alpha Fc receptor level in Chronic kidney disease with hypertension and no diabetes (4987_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 immunoglobulin alpha fc receptor measurement http://www.ebi.ac.uk/efo/EFO_0020462 GCST90237778 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet glycoprotein Ib alpha chain level in Chronic kidney disease with hypertension and no diabetes (4990_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet glycoprotein ib alpha chain measurement http://www.ebi.ac.uk/efo/EFO_0020645 GCST90237779 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glypican-5 level in Chronic kidney disease with hypertension and no diabetes (4991_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 glypican-5 measurement http://www.ebi.ac.uk/efo/EFO_0008139 GCST90237780 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulins level in Chronic kidney disease with hypertension and no diabetes (4992_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 granulins measurement http://www.ebi.ac.uk/efo/EFO_0008141 GCST90237781 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase A3 level in Chronic kidney disease with hypertension and no diabetes (4993_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 glutathione s-transferase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020409 GCST90237782 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 15-hydroxyprostaglandin dehydrogenase [NAD(+)] level in Chronic kidney disease with hypertension and no diabetes (4995_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 15-hydroxyprostaglandin dehydrogenase [NAD(+)] in blood serum http://purl.obolibrary.org/obo/OBA_2041922 GCST90237783 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic initiation factor 4A-III level in Chronic kidney disease with hypertension and no diabetes (4997_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 eukaryotic initiation factor 4a-III measurement http://www.ebi.ac.uk/efo/EFO_0020366 GCST90237784 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-3-binding protein level in Chronic kidney disease with hypertension and no diabetes (5000_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-3-binding protein measurement http://www.ebi.ac.uk/efo/EFO_0010241 GCST90237785 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mammaglobin-B level in Chronic kidney disease with hypertension and no diabetes (5001_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 mammaglobin-b measurement http://www.ebi.ac.uk/efo/EFO_0020552 GCST90237786 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-14 level in Chronic kidney disease with hypertension and no diabetes (5002_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrix metalloproteinase-14 measurement http://www.ebi.ac.uk/efo/EFO_0020558 GCST90237787 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 11 level in Chronic kidney disease with hypertension and no diabetes (5004_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 11 measurement http://www.ebi.ac.uk/efo/EFO_0020575 GCST90237788 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 12 level in Chronic kidney disease with hypertension and no diabetes (5005_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 12 measurement http://www.ebi.ac.uk/efo/EFO_0020576 GCST90237789 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 13 level in Chronic kidney disease with hypertension and no diabetes (5006_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 13 measurement http://www.ebi.ac.uk/efo/EFO_0020577 GCST90237790 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 14 level in Chronic kidney disease with hypertension and no diabetes (5007_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 14 measurement http://www.ebi.ac.uk/efo/EFO_0020578 GCST90237791 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Superoxide dismutase [Mn], mitochondrial level in Chronic kidney disease with hypertension and no diabetes (5008_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of superoxide dismutase [Mn], mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043595 GCST90237792 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Moesin level in Chronic kidney disease with hypertension and no diabetes (5009_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 moesin measurement http://www.ebi.ac.uk/efo/EFO_0020583 GCST90237793 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nicotinamide phosphoribosyltransferase level in Chronic kidney disease with hypertension and no diabetes (5011_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 nicotinamide phosphoribosyltransferase measurement http://www.ebi.ac.uk/efo/EFO_0020607 GCST90237794 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenylate kinase isoenzyme 1 level in Chronic kidney disease with hypertension and no diabetes (5012_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 adenylate kinase isoenzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0020129 GCST90237795 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chloride intracellular channel protein 1 level in Chronic kidney disease with hypertension and no diabetes (5013_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 chloride intracellular channel protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020256 GCST90237796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoplasmic protein NCK1 level in Chronic kidney disease with hypertension and no diabetes (5014_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytoplasmic protein NCK1 measurement http://www.ebi.ac.uk/efo/EFO_0020307 GCST90237797 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-activating factor acetylhydrolase level in Chronic kidney disease with hypertension and no diabetes (5015_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet-activating factor acetylhydrolase measurement http://www.ebi.ac.uk/efo/EFO_0020647 GCST90237798 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxiredoxin-5, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (5017_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 peroxiredoxin-5, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020630 GCST90237799 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxiredoxin-6 level in Chronic kidney disease with hypertension and no diabetes (5018_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 peroxiredoxin-6 measurement http://www.ebi.ac.uk/efo/EFO_0020631 GCST90237800 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase isozyme L1 level in Chronic kidney disease with hypertension and no diabetes (5019_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin carboxyl-terminal hydrolase isozyme L1 measurement http://www.ebi.ac.uk/efo/EFO_0020838 GCST90237801 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoglycerate kinase 1 level in Chronic kidney disease with hypertension and no diabetes (5020_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 phosphoglycerate kinase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020638 GCST90237802 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inorganic pyrophosphatase level in Chronic kidney disease with hypertension and no diabetes (5021_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 inorganic pyrophosphatase measurement http://www.ebi.ac.uk/efo/EFO_0008157 GCST90237803 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenylosuccinate lyase level in Chronic kidney disease with hypertension and no diabetes (5023_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 adenylosuccinate lyase measurement http://www.ebi.ac.uk/efo/EFO_0020130 GCST90237804 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoblastoma-associated protein level in Chronic kidney disease with hypertension and no diabetes (5024_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 retinoblastoma-associated protein measurement http://www.ebi.ac.uk/efo/EFO_0020706 GCST90237805 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S3 level in Chronic kidney disease with hypertension and no diabetes (5026_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 40s ribosomal protein S3 measurement http://www.ebi.ac.uk/efo/EFO_0020117 GCST90237806 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor cysteine-rich type 1 protein M130 level in Chronic kidney disease with hypertension and no diabetes (5028_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 scavenger receptor cysteine-rich type 1 protein m130 measurement http://www.ebi.ac.uk/efo/EFO_0020717 GCST90237807 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolyl endopeptidase FAP level in Chronic kidney disease with hypertension and no diabetes (5029_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 prolyl endopeptidase FAP measurement http://www.ebi.ac.uk/efo/EFO_0021856 GCST90237808 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD-dependent protein deacetylase sirtuin-2 level in Chronic kidney disease with hypertension and no diabetes (5030_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 NAD-dependent protein deacetylase sirtuin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008241 GCST90237809 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spectrin alpha chain, non-erythrocytic 1 level in Chronic kidney disease with hypertension and no diabetes (5031_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 spectrin alpha chain, non-erythrocytic 1 measurement http://www.ebi.ac.uk/efo/EFO_0020749 GCST90237810 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FACT complex subunit SSRP1 level in Chronic kidney disease with hypertension and no diabetes (5032_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 fact complex subunit ssrp1 measurement http://www.ebi.ac.uk/efo/EFO_0020371 GCST90237811 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomyosin alpha-1 chain level in Chronic kidney disease with hypertension and no diabetes (5033_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 tropomyosin alpha-1 chain measurement http://www.ebi.ac.uk/efo/EFO_0020786 GCST90237812 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trypsin-2 level in Chronic kidney disease with hypertension and no diabetes (5034_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 trypsin-2 measurement http://www.ebi.ac.uk/efo/EFO_0008305 GCST90237813 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thymidylate synthase level in Chronic kidney disease with hypertension and no diabetes (5035_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 thymidylate synthase measurement http://www.ebi.ac.uk/efo/EFO_0020774 GCST90237814 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor-inducible gene 6 protein level in Chronic kidney disease with hypertension and no diabetes (5036_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor-inducible gene 6 protein measurement http://www.ebi.ac.uk/efo/EFO_0008311 GCST90237815 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death 1 ligand 1 level in Chronic kidney disease with hypertension and no diabetes (5060_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 programmed cell death 1 ligand 1 measurement http://www.ebi.ac.uk/efo/EFO_0020654 GCST90237816 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ICOS ligand level in Chronic kidney disease with hypertension and no diabetes (5061_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90237817 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD226 antigen level in Chronic kidney disease with hypertension and no diabetes (5062_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD226 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020246 GCST90237818 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Natural killer cell receptor 2B4 level in Chronic kidney disease with hypertension and no diabetes (5063_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 natural killer cell receptor 2B4 measurement http://www.ebi.ac.uk/efo/EFO_0021882 GCST90237819 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD83 antigen level in Chronic kidney disease with hypertension and no diabetes (5065_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD83 antigen measurement http://www.ebi.ac.uk/efo/EFO_0021983 GCST90237820 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 6 level in Chronic kidney disease with hypertension and no diabetes (5066_134) 466 African American individuals NA Illumina [14870897] (imputed) 1 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90237821 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement decay-accelerating factor level in Chronic kidney disease with hypertension and no diabetes (5069_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement decay-accelerating factor measurement http://www.ebi.ac.uk/efo/EFO_0008095 GCST90237822 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 6B level in Chronic kidney disease with hypertension and no diabetes (5070_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 6B measurement http://www.ebi.ac.uk/efo/EFO_0020815 GCST90237823 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 10 level in Chronic kidney disease with hypertension and no diabetes (5076_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-a receptor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020350 GCST90237824 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-B receptor 6 level in Chronic kidney disease with hypertension and no diabetes (5078_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90237825 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane glycoprotein NMB level in Chronic kidney disease with hypertension and no diabetes (5080_131) 466 African American individuals NA Illumina [14870897] (imputed) 0 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90237826 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. X-linked interleukin-1 receptor accessory protein-like 2 level in Chronic kidney disease with hypertension and no diabetes (5082_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 x-linked interleukin-1 receptor accessory protein-like 2 measurement http://www.ebi.ac.uk/efo/EFO_0020854 GCST90237827 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17 receptor B level in Chronic kidney disease with hypertension and no diabetes (5084_154) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-17 receptor B in blood serum http://purl.obolibrary.org/obo/OBA_2042002 GCST90237828 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-20 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (5085_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-20 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020497 GCST90237829 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-22 receptor subunit alpha-2 level in Chronic kidney disease with hypertension and no diabetes (5087_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90237830 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-23 receptor level in Chronic kidney disease with hypertension and no diabetes (5088_175) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-23 receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042013 GCST90237831 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-7 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (5089_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-7 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0020508 GCST90237832 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily B member 1 level in Chronic kidney disease with hypertension and no diabetes (5090_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 leukocyte immunoglobulin-like receptor subfamily B member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008208 GCST90237833 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily B member 2 level in Chronic kidney disease with hypertension and no diabetes (5091_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90237834 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein jagged-1 level in Chronic kidney disease with hypertension and no diabetes (5092_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein jagged-1 measurement http://www.ebi.ac.uk/efo/EFO_0008271 GCST90237835 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein jagged-2 level in Chronic kidney disease with hypertension and no diabetes (5093_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein jagged-2 measurement http://www.ebi.ac.uk/efo/EFO_0020675 GCST90237836 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctional adhesion molecule-like level in Chronic kidney disease with hypertension and no diabetes (5094_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 junctional adhesion molecule-like measurement http://www.ebi.ac.uk/efo/EFO_0020511 GCST90237837 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DL4 level in Chronic kidney disease with hypertension and no diabetes (5095_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90237838 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin-dependent peroxide reductase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8358_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thioredoxin-dependent peroxide reductase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043020 GCST90238909 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase 17B level in Chronic kidney disease with hypertension and no diabetes (8359_149) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase 17B measurement http://www.ebi.ac.uk/efo/EFO_0008281 GCST90238910 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Natural cytotoxicity triggering receptor 1 level in Chronic kidney disease with hypertension and no diabetes (8360_169) 466 African American individuals NA Illumina [14870897] (imputed) 0 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90238911 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0577 protein KIAA1324-like level in Chronic kidney disease with hypertension and no diabetes (8363_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endosome/lysosome-associated apoptosis and autophagy regulator family member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044817 GCST90238912 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uronyl 2-sulfotransferase level in Chronic kidney disease with hypertension and no diabetes (8364_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uronyl 2-sulfotransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044069 GCST90238913 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C1orf115 level in Chronic kidney disease with hypertension and no diabetes (8366_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of required for drug-induced death protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044876 GCST90238914 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and immunoglobulin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8367_142) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-set and immunoglobulin domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044565 GCST90238915 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 1B level in Chronic kidney disease with hypertension and no diabetes (8368_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 1B measurement http://www.ebi.ac.uk/efo/EFO_0010624 GCST90238916 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dystroglycan level in Chronic kidney disease with hypertension and no diabetes (8369_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dystroglycan 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041225 GCST90238917 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-related family member 1 level in Chronic kidney disease with hypertension and no diabetes (8372_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-related family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042782 GCST90238918 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 16 level in Chronic kidney disease with hypertension and no diabetes (8374_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor necrosis factor receptor superfamily member 16 in blood serum http://purl.obolibrary.org/obo/OBA_2040296 GCST90238919 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lutropin subunit beta level in Chronic kidney disease with hypertension and no diabetes (8376_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lutropin subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2042192 GCST90238920 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein LDOC1 level in Chronic kidney disease with hypertension and no diabetes (8378_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein LDOC1 in blood serum http://purl.obolibrary.org/obo/OBA_2042184 GCST90238921 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein delta homolog 1 level in Chronic kidney disease with hypertension and no diabetes (8380_244) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein delta homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041313 GCST90238922 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C11orf94 level in Chronic kidney disease with hypertension and no diabetes (8383_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Frey in blood serum http://purl.obolibrary.org/obo/OBA_2044818 GCST90238923 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte growth factor activator level in Chronic kidney disease with hypertension and no diabetes (8385_248) 466 African American individuals NA Illumina [14870897] (imputed) 1 hepatocyte growth factor activator measurement http://www.ebi.ac.uk/efo/EFO_0008152 GCST90238924 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostate and testis expressed protein 1 level in Chronic kidney disease with hypertension and no diabetes (8386_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostate and testis expressed protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042766 GCST90238925 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spastin level in Chronic kidney disease with hypertension and no diabetes (8388_24) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238926 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 74A level in Chronic kidney disease with hypertension and no diabetes (8389_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 74A in blood serum http://purl.obolibrary.org/obo/OBA_2044824 GCST90238927 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase subunit 7A1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8390_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome c oxidase subunit 7A1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041109 GCST90238928 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 115 level in Chronic kidney disease with hypertension and no diabetes (8391_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 115 in blood serum http://purl.obolibrary.org/obo/OBA_2041274 GCST90238929 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin F level in Chronic kidney disease with hypertension and no diabetes (8393_121) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin F measurement http://www.ebi.ac.uk/efo/EFO_0022038 GCST90238930 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Non-secretory ribonuclease level in Chronic kidney disease with hypertension and no diabetes (8394_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of non-secretory ribonuclease in blood serum http://purl.obolibrary.org/obo/OBA_2043283 GCST90238931 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty-acid amide hydrolase 2 level in Chronic kidney disease with hypertension and no diabetes (8396_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fatty-acid amide hydrolase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041537 GCST90238932 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfhydryl oxidase 2 level in Chronic kidney disease with hypertension and no diabetes (8397_147) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sulfhydryl oxidase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043136 GCST90238933 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sprouty-related, EVH1 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8318_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sprouty-related, EVH1 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043644 GCST90238884 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SAFB-like transcription modulator level in Chronic kidney disease with hypertension and no diabetes (8320_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SAFB-like transcription modulator in blood serum http://purl.obolibrary.org/obo/OBA_2043551 GCST90238885 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 843 level in Chronic kidney disease with hypertension and no diabetes (8321_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 843 in blood serum http://purl.obolibrary.org/obo/OBA_2044216 GCST90238886 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trefoil factor 3 level in Chronic kidney disease with hypertension and no diabetes (8323_163) 466 African American individuals NA Illumina [14870897] (imputed) 0 trefoil factor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008304 GCST90238887 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase 4 level in Chronic kidney disease with hypertension and no diabetes (8325_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of all-trans-retinol dehydrogenase [NAD(+)] ADH4 in blood serum http://purl.obolibrary.org/obo/OBA_2040516 GCST90238888 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Single Ig IL-1-related receptor level in Chronic kidney disease with hypertension and no diabetes (8326_63) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of single Ig IL-1-related receptor in blood serum http://purl.obolibrary.org/obo/OBA_2043507 GCST90238889 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dipeptidase 2 level in Chronic kidney disease with hypertension and no diabetes (8327_26) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of dipeptidase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041349 GCST90238890 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ethanolamine kinase 1 level in Chronic kidney disease with hypertension and no diabetes (8328_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ethanolamine kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041515 GCST90238891 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-12 level in Chronic kidney disease with hypertension and no diabetes (8329_166) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020210 GCST90238892 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 11 level in Chronic kidney disease with hypertension and no diabetes (8330_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of low-density lipoprotein receptor-related protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042229 GCST90238893 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-complex protein 11 homolog level in Chronic kidney disease with hypertension and no diabetes (8334_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-complex protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2043817 GCST90238894 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRAM domain-containing protein 1C level in Chronic kidney disease with hypertension and no diabetes (8336_267) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Aster-C in blood serum http://purl.obolibrary.org/obo/OBA_2044781 GCST90238895 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-type tyrosine-protein phosphatase U level in Chronic kidney disease with hypertension and no diabetes (8337_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-type tyrosine-protein phosphatase U in blood serum http://purl.obolibrary.org/obo/OBA_2043110 GCST90238896 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 110 level in Chronic kidney disease with hypertension and no diabetes (8340_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 110 in blood serum http://purl.obolibrary.org/obo/OBA_2041271 GCST90238897 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly(A) polymerase gamma level in Chronic kidney disease with hypertension and no diabetes (8343_224) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of poly(A) polymerase gamma in blood serum http://purl.obolibrary.org/obo/OBA_2042759 GCST90238898 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione peroxidase 7 level in Chronic kidney disease with hypertension and no diabetes (8345_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione peroxidase 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041781 GCST90238899 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dipeptidyl peptidase 2 level in Chronic kidney disease with hypertension and no diabetes (8346_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 dipeptidyl peptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020326 GCST90238900 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 129 level in Chronic kidney disease with hypertension and no diabetes (8347_222) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 129 in blood serum http://purl.obolibrary.org/obo/OBA_2041282 GCST90238901 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-B receptor 2 level in Chronic kidney disease with hypertension and no diabetes (8348_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-B receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008124 GCST90238902 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease 57 level in Chronic kidney disease with hypertension and no diabetes (8351_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine protease 57 in blood serum http://purl.obolibrary.org/obo/OBA_2043049 GCST90238903 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 12 level in Chronic kidney disease with hypertension and no diabetes (8352_26) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238904 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium channel subunit beta-2 level in Chronic kidney disease with hypertension and no diabetes (8353_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium channel subunit beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043404 GCST90238905 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isthmin-1 level in Chronic kidney disease with hypertension and no diabetes (8355_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isthmin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042044 GCST90238906 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxytocin-neurophysin 1 level in Chronic kidney disease with hypertension and no diabetes (8356_88) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of oxytocin-neurophysin 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042729 GCST90238907 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfotransferase 4A1 level in Chronic kidney disease with hypertension and no diabetes (8357_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 4A1 in blood serum http://purl.obolibrary.org/obo/OBA_2043730 GCST90238908 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BMP and activin membrane-bound inhibitor homolog level in Chronic kidney disease with hypertension and no diabetes (8811_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239034 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin level in Chronic kidney disease with hypertension and no diabetes (8813_160) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thioredoxin in blood serum http://purl.obolibrary.org/obo/OBA_2043965 GCST90239035 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proactivator polypeptide-like 1 level in Chronic kidney disease with hypertension and no diabetes (8814_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proactivator polypeptide-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043051 GCST90239036 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Olfactomedin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (8815_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of olfactomedin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042703 GCST90239037 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centromere protein V level in Chronic kidney disease with hypertension and no diabetes (8817_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centromere protein V in blood serum http://purl.obolibrary.org/obo/OBA_2040986 GCST90239038 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon gamma receptor 2 level in Chronic kidney disease with hypertension and no diabetes (8818_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90239039 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (8819_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90239040 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paired immunoglobulin-like type 2 receptor alpha level in Chronic kidney disease with hypertension and no diabetes (8825_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of paired immunoglobulin-like type 2 receptor alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042892 GCST90239041 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epithelial splicing regulatory protein 1 level in Chronic kidney disease with hypertension and no diabetes (8828_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epithelial splicing regulatory protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041512 GCST90239042 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRISC complex subunit Abro1 level in Chronic kidney disease with hypertension and no diabetes (8830_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRISC complex subunit Abraxas 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044537 GCST90239043 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone marrow stromal antigen 2 level in Chronic kidney disease with hypertension and no diabetes (8832_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone marrow stromal antigen 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040266 GCST90239044 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 10 level in Chronic kidney disease with hypertension and no diabetes (8833_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 10 measurement http://www.ebi.ac.uk/efo/EFO_0010800 GCST90239045 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calnexin level in Chronic kidney disease with hypertension and no diabetes (8834_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calnexin in blood serum http://purl.obolibrary.org/obo/OBA_2040887 GCST90239046 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microfibrillar-associated protein 3-like level in Chronic kidney disease with hypertension and no diabetes (8837_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of microfibrillar-associated protein 3-like in blood serum http://purl.obolibrary.org/obo/OBA_2042351 GCST90239047 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein CASC4 level in Chronic kidney disease with hypertension and no diabetes (8838_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein GOLM2 in blood serum http://purl.obolibrary.org/obo/OBA_2040903 GCST90239048 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metaxin-2 level in Chronic kidney disease with hypertension and no diabetes (8839_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of metaxin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042458 GCST90239049 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1s subcomponent level in Chronic kidney disease with hypertension and no diabetes (8840_61) 466 African American individuals NA Illumina [14870897] (imputed) 1 complement C1s subcomponent measurement http://www.ebi.ac.uk/efo/EFO_0008091 GCST90239050 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cartilage intermediate layer protein 2 level in Chronic kidney disease with hypertension and no diabetes (8841_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cartilage intermediate layer protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041031 GCST90239051 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRAM domain-containing protein 1C level in Chronic kidney disease with hypertension and no diabetes (8842_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Aster-C in blood serum http://purl.obolibrary.org/obo/OBA_2044781 GCST90239052 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myelin regulatory factor level in Chronic kidney disease with hypertension and no diabetes (8843_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon regulatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021908 GCST90239053 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. A disintegrin and metalloproteinase with thrombospondin motifs 3 level in Chronic kidney disease with hypertension and no diabetes (8845_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of a disintegrin and metalloproteinase with thrombospondin motifs 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040505 GCST90239054 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative inactive group IIC secretory phospholipase A2 level in Chronic kidney disease with hypertension and no diabetes (8850_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of group IIC secretory phospholipase A2 in blood serum http://purl.obolibrary.org/obo/OBA_2043128 GCST90239055 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM171B level in Chronic kidney disease with hypertension and no diabetes (8851_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239056 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SUN domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (8852_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SUN domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044231 GCST90239057 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 4 member A level in Chronic kidney disease with hypertension and no diabetes (8853_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 4 member A in blood serum http://purl.obolibrary.org/obo/OBA_2041046 GCST90239058 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonucleoside-diphosphate reductase subunit M2 B level in Chronic kidney disease with hypertension and no diabetes (8854_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonucleoside-diphosphate reductase subunit M2 B in blood serum http://purl.obolibrary.org/obo/OBA_2043348 GCST90239059 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Basic leucine zipper transcriptional factor ATF-like 3 level in Chronic kidney disease with hypertension and no diabetes (8858_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of basic leucine zipper transcriptional factor ATF-like 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040782 GCST90239060 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 3-kinase regulatory subunit alpha level in Chronic kidney disease with hypertension and no diabetes (8863_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol 3-kinase regulatory subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042891 GCST90239061 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centromere protein W level in Chronic kidney disease with hypertension and no diabetes (8864_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of centromere protein W in blood serum http://purl.obolibrary.org/obo/OBA_2044399 GCST90239062 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaminyl-peptide cyclotransferase-like protein level in Chronic kidney disease with hypertension and no diabetes (8866_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutaminyl-peptide cyclotransferase-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2043132 GCST90239063 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycodelin level in Chronic kidney disease with hypertension and no diabetes (8867_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycodelin in blood serum http://purl.obolibrary.org/obo/OBA_2042743 GCST90239064 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin subfamily 2 member A1 level in Chronic kidney disease with hypertension and no diabetes (8869_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of butyrophilin subfamily 2 member A1 in blood serum http://purl.obolibrary.org/obo/OBA_2044699 GCST90239065 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleophosmin level in Chronic kidney disease with hypertension and no diabetes (8870_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleophosmin in blood serum http://purl.obolibrary.org/obo/OBA_2042616 GCST90239066 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear migration protein nudC level in Chronic kidney disease with hypertension and no diabetes (8871_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239067 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein transport protein Sec61 subunit gamma level in Chronic kidney disease with hypertension and no diabetes (8872_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein transport protein Sec61 subunit gamma in blood serum http://purl.obolibrary.org/obo/OBA_2043421 GCST90239068 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ceroid-lipofuscinosis neuronal protein 5 level in Chronic kidney disease with hypertension and no diabetes (8874_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239069 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexin-2-beta level in Chronic kidney disease with hypertension and no diabetes (8876_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurexin-2-beta in blood serum http://purl.obolibrary.org/obo/OBA_2044801 GCST90239070 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein eva-1 homolog C level in Chronic kidney disease with hypertension and no diabetes (8877_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239071 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. YTH domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8878_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of YTH domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044165 GCST90239072 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 17 level in Chronic kidney disease with hypertension and no diabetes (8882_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239073 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Voltage-dependent calcium channel subunit alpha-2/delta-3 level in Chronic kidney disease with hypertension and no diabetes (8885_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-dependent calcium channel subunit alpha-2/delta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040868 GCST90239074 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear migration protein nudC level in Chronic kidney disease with hypertension and no diabetes (8887_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239075 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small integral membrane protein 9 level in Chronic kidney disease with hypertension and no diabetes (8888_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small integral membrane protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2044815 GCST90239076 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell cycle progression protein 1 level in Chronic kidney disease with hypertension and no diabetes (8889_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell cycle progression protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040937 GCST90239077 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 132B level in Chronic kidney disease with hypertension and no diabetes (8890_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 132B in blood serum http://purl.obolibrary.org/obo/OBA_2044705 GCST90239078 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable serine carboxypeptidase CPVL level in Chronic kidney disease with hypertension and no diabetes (8891_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of probable serine carboxypeptidase CPVL in blood serum http://purl.obolibrary.org/obo/OBA_2044639 GCST90239079 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet endothelial aggregation receptor 1 level in Chronic kidney disease with hypertension and no diabetes (8892_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239080 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly [ADP-ribose] polymerase 1 level in Chronic kidney disease with hypertension and no diabetes (8893_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239081 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein A/B level in Chronic kidney disease with hypertension and no diabetes (8894_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 heterogeneous nuclear ribonucleoprotein a/b measurement http://www.ebi.ac.uk/efo/EFO_0020441 GCST90239082 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 37A2 level in Chronic kidney disease with hypertension and no diabetes (8897_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 37A2 in blood serum http://purl.obolibrary.org/obo/OBA_2044554 GCST90239083 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Erythroid membrane-associated protein level in Chronic kidney disease with hypertension and no diabetes (8631_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of erythroid membrane-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2041505 GCST90238984 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF128 level in Chronic kidney disease with hypertension and no diabetes (8633_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238985 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zona pellucida-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (8635_283) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zona pellucida-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044218 GCST90238986 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin H level in Chronic kidney disease with hypertension and no diabetes (8644_46) 466 African American individuals NA Illumina [14870897] (imputed) 1 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90238987 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal membrane protein PEX14 level in Chronic kidney disease with hypertension and no diabetes (8645_257) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238988 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane neuronal protein 4 level in Chronic kidney disease with hypertension and no diabetes (8646_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238989 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (8654_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238990 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein G6b level in Chronic kidney disease with hypertension and no diabetes (8659_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238991 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Olfactomedin-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (8660_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of olfactomedin-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042704 GCST90238992 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Extracellular tyrosine-protein kinase PKDCC level in Chronic kidney disease with hypertension and no diabetes (8664_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of extracellular tyrosine-protein kinase PKDCC in blood serum http://purl.obolibrary.org/obo/OBA_2043485 GCST90238993 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trafficking protein particle complex subunit 5 level in Chronic kidney disease with hypertension and no diabetes (8671_378) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trafficking protein particle complex subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043921 GCST90238994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane-associated progesterone receptor component 2 level in Chronic kidney disease with hypertension and no diabetes (8681_93) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane-associated progesterone receptor component 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042870 GCST90238995 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Hikeshi level in Chronic kidney disease with hypertension and no diabetes (8686_342) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Hikeshi in blood serum http://purl.obolibrary.org/obo/OBA_2044806 GCST90238996 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 106B level in Chronic kidney disease with hypertension and no diabetes (8687_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 106B in blood serum http://purl.obolibrary.org/obo/OBA_2044362 GCST90238997 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caveolin-3 level in Chronic kidney disease with hypertension and no diabetes (8690_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caveolin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040909 GCST90238998 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galactosylceramide sulfotransferase level in Chronic kidney disease with hypertension and no diabetes (8696_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of galactosylceramide sulfotransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041655 GCST90238999 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glypican-1 level in Chronic kidney disease with hypertension and no diabetes (8697_38) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glypican-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041768 GCST90239000 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich motor neuron 1 protein level in Chronic kidney disease with hypertension and no diabetes (8699_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239001 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 11 level in Chronic kidney disease with hypertension and no diabetes (8700_325) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 11 in blood serum http://purl.obolibrary.org/obo/OBA_2041661 GCST90239002 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteoclast-associated immunoglobulin-like receptor level in Chronic kidney disease with hypertension and no diabetes (8702_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of osteoclast-associated immunoglobulin-like receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042715 GCST90239003 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HLA class II histocompatibility antigen gamma chain level in Chronic kidney disease with hypertension and no diabetes (8748_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MHC class II histocompatibility antigen gamma chain in blood serum http://purl.obolibrary.org/obo/OBA_2040331 GCST90239004 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Antigen-presenting glycoprotein CD1d level in Chronic kidney disease with hypertension and no diabetes (8749_194) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of antigen-presenting glycoprotein CD1d in blood serum http://purl.obolibrary.org/obo/OBA_2040368 GCST90239005 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vinculin level in Chronic kidney disease with hypertension and no diabetes (8750_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vinculin in blood serum http://purl.obolibrary.org/obo/OBA_2044089 GCST90239006 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuromedin-U level in Chronic kidney disease with hypertension and no diabetes (8754_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuromedin-U in blood serum http://purl.obolibrary.org/obo/OBA_2042602 GCST90239007 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Potassium voltage-gated channel subfamily E regulatory beta subunit 5 level in Chronic kidney disease with hypertension and no diabetes (8756_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239008 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arylsulfatase K level in Chronic kidney disease with hypertension and no diabetes (8269_327) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arylsulfatase K in blood serum http://purl.obolibrary.org/obo/OBA_2040686 GCST90238859 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-keto-steroid reductase level in Chronic kidney disease with hypertension and no diabetes (8272_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238860 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-31 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (8273_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-31 receptor A in blood serum http://purl.obolibrary.org/obo/OBA_2042016 GCST90238861 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-7 level in Chronic kidney disease with hypertension and no diabetes (8274_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-7 in blood serum http://purl.obolibrary.org/obo/OBA_2043717 GCST90238862 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet endothelial aggregation receptor 1 level in Chronic kidney disease with hypertension and no diabetes (8275_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238863 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitronectin level in Chronic kidney disease with hypertension and no diabetes (8280_238) 466 African American individuals NA Illumina [14870897] (imputed) 0 vitronectin measurement http://www.ebi.ac.uk/efo/EFO_0021843 GCST90238864 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pituitary adenylate cyclase-activating polypeptide level in Chronic kidney disease with hypertension and no diabetes (8285_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pituitary adenylate cyclase-activating polypeptide in blood serum http://purl.obolibrary.org/obo/OBA_2040510 GCST90238865 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 2 level in Chronic kidney disease with hypertension and no diabetes (8287_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMRF35-like molecule 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040298 GCST90238866 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-2-glycoprotein 1 level in Chronic kidney disease with hypertension and no diabetes (8288_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-2-glycoprotein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040629 GCST90238867 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane glycoprotein NMB level in Chronic kidney disease with hypertension and no diabetes (8289_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90238868 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noelin-2 level in Chronic kidney disease with hypertension and no diabetes (8295_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of noelin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042702 GCST90238869 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. KDEL motif-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (8296_117) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein O-glucosyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044322 GCST90238870 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 10 level in Chronic kidney disease with hypertension and no diabetes (8297_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041331 GCST90238871 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine-rich single-pass membrane protein 1 level in Chronic kidney disease with hypertension and no diabetes (8298_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine-rich single-pass membrane protein 1 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044917 GCST90238872 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily A member 4 level in Chronic kidney disease with hypertension and no diabetes (8299_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte immunoglobulin-like receptor subfamily A member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040294 GCST90238873 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal membrane protein PEX14 level in Chronic kidney disease with hypertension and no diabetes (8300_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238874 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0160 protein MYG1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8303_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MYG1 exonuclease in blood serum http://purl.obolibrary.org/obo/OBA_2044877 GCST90238875 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 11B level in Chronic kidney disease with hypertension and no diabetes (8304_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 11B measurement http://www.ebi.ac.uk/efo/EFO_0020801 GCST90238876 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Extracellular sulfatase Sulf-2 level in Chronic kidney disease with hypertension and no diabetes (8305_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of extracellular sulfatase Sulf-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043724 GCST90238877 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane gamma-carboxyglutamic acid protein 1 level in Chronic kidney disease with hypertension and no diabetes (8306_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238878 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0696 protein C11orf68 level in Chronic kidney disease with hypertension and no diabetes (8307_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UPF0696 protein C11orf68 in blood serum http://purl.obolibrary.org/obo/OBA_2044871 GCST90238879 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hyaluronidase-1 level in Chronic kidney disease with hypertension and no diabetes (8309_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hyaluronidase-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041961 GCST90238880 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UMP-CMP kinase level in Chronic kidney disease with hypertension and no diabetes (8312_139) 466 African American individuals NA Illumina [14870897] (imputed) 0 UMP-CMP kinase measurement http://www.ebi.ac.uk/efo/EFO_0008313 GCST90238881 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylglucosamine-6-sulfatase level in Chronic kidney disease with hypertension and no diabetes (8314_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 n-acetylglucosamine-6-sulfatase measurement http://www.ebi.ac.uk/efo/EFO_0020586 GCST90238882 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 119 level in Chronic kidney disease with hypertension and no diabetes (8315_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 119 in blood serum http://purl.obolibrary.org/obo/OBA_2041277 GCST90238883 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostate-specific antigen level in Chronic kidney disease with hypertension and no diabetes (8468_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 prostate specific antigen measurement http://www.ebi.ac.uk/efo/EFO_0004624 GCST90238959 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (8469_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 insulin-like growth factor-binding protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020475 GCST90238960 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease H1 level in Chronic kidney disease with hypertension and no diabetes (8470_213) 466 African American individuals NA Illumina [14870897] (imputed) 0 ribonuclease H1 measurement http://www.ebi.ac.uk/efo/EFO_0022020 GCST90238961 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive tyrosine-protein kinase transmembrane receptor ROR1 level in Chronic kidney disease with hypertension and no diabetes (8474_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tyrosine-protein kinase transmembrane receptor ROR1 in blood serum http://purl.obolibrary.org/obo/OBA_2043309 GCST90238962 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrilysin level in Chronic kidney disease with hypertension and no diabetes (8475_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrilysin measurement http://www.ebi.ac.uk/efo/EFO_0008227 GCST90238963 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromogranin-A level in Chronic kidney disease with hypertension and no diabetes (8476_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 chromogranin-A measurement http://www.ebi.ac.uk/efo/EFO_0022021 GCST90238964 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromelysin-2 level in Chronic kidney disease with hypertension and no diabetes (8479_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stromelysin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042387 GCST90238965 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EGF-containing fibulin-like extracellular matrix protein 1 level in Chronic kidney disease with hypertension and no diabetes (8480_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 EGF-containing fibulin-like extracellular matrix protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0022022 GCST90238966 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leptin level in Chronic kidney disease with hypertension and no diabetes (8484_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 leptin measurement http://www.ebi.ac.uk/efo/EFO_0005000 GCST90238967 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like ECH-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (8485_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 kelch-like ECH-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0022023 GCST90238968 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-IIb: beta-3 complex level in Chronic kidney disease with hypertension and no diabetes (8488_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-IIb: beta-3 complex measurement http://www.ebi.ac.uk/efo/EFO_0020479 GCST90238969 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 30 level in Chronic kidney disease with hypertension and no diabetes (8520_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 30 in blood serum http://purl.obolibrary.org/obo/OBA_2040501 GCST90238970 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily containing leucine-rich repeat protein 2 level in Chronic kidney disease with hypertension and no diabetes (8528_74) 466 African American individuals NA Illumina [14870897] (imputed) 1 immunoglobulin superfamily containing leucine-rich repeat protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021879 GCST90238971 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 10B level in Chronic kidney disease with hypertension and no diabetes (8529_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 10B measurement http://www.ebi.ac.uk/efo/EFO_0021993 GCST90238972 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dermokine level in Chronic kidney disease with hypertension and no diabetes (8535_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dermokine in blood serum http://purl.obolibrary.org/obo/OBA_2041322 GCST90238973 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C17orf78 level in Chronic kidney disease with hypertension and no diabetes (8545_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238974 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM134B level in Chronic kidney disease with hypertension and no diabetes (8556_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of reticulophagy regulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044521 GCST90238975 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plasmalemma vesicle-associated protein level in Chronic kidney disease with hypertension and no diabetes (8565_160) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plasmalemma vesicle-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2042936 GCST90238976 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 8B level in Chronic kidney disease with hypertension and no diabetes (8569_147) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 8B in blood serum http://purl.obolibrary.org/obo/OBA_2040676 GCST90238977 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 14 level in Chronic kidney disease with hypertension and no diabetes (8587_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine protease inhibitor Kazal-type 14 in blood serum http://purl.obolibrary.org/obo/OBA_2044789 GCST90238978 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUB domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8589_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CUB domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040956 GCST90238979 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 9 level in Chronic kidney disease with hypertension and no diabetes (8597_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238980 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 1, soluble level in Chronic kidney disease with hypertension and no diabetes (8601_167) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238981 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane glycoprotein NMB level in Chronic kidney disease with hypertension and no diabetes (8606_39) 466 African American individuals NA Illumina [14870897] (imputed) 1 transmembrane glycoprotein NMB measurement http://www.ebi.ac.uk/efo/EFO_0008303 GCST90238982 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5D level in Chronic kidney disease with hypertension and no diabetes (8624_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90238983 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin alpha-7 level in Chronic kidney disease with hypertension and no diabetes (8758_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin alpha-7 in blood serum http://purl.obolibrary.org/obo/OBA_2042786 GCST90239009 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactosylceramide 4-alpha-galactosyltransferase level in Chronic kidney disease with hypertension and no diabetes (8759_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lactosylceramide 4-alpha-galactosyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2040451 GCST90239010 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DCN1-like protein 5 level in Chronic kidney disease with hypertension and no diabetes (8760_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of DCN1-like protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041249 GCST90239011 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD70 antigen level in Chronic kidney disease with hypertension and no diabetes (8762_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD70 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020249 GCST90239012 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily A member 5 level in Chronic kidney disease with hypertension and no diabetes (8766_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily A member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042197 GCST90239013 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelin-converting enzyme 1 level in Chronic kidney disease with hypertension and no diabetes (8767_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 endothelin-converting enzyme 1 measurement http://www.ebi.ac.uk/efo/EFO_0008121 GCST90239014 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell lymphoma/leukemia 10 level in Chronic kidney disease with hypertension and no diabetes (8768_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell lymphoma/leukemia 10 in blood serum http://purl.obolibrary.org/obo/OBA_2040787 GCST90239015 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-B2 level in Chronic kidney disease with hypertension and no diabetes (8772_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239016 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EMILIN-3 level in Chronic kidney disease with hypertension and no diabetes (8773_172) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239017 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM24B level in Chronic kidney disease with hypertension and no diabetes (8775_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM24B in blood serum http://purl.obolibrary.org/obo/OBA_2044393 GCST90239018 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Erlin-1 level in Chronic kidney disease with hypertension and no diabetes (8776_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of erlin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041504 GCST90239019 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noggin level in Chronic kidney disease with hypertension and no diabetes (8778_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 noggin measurement http://www.ebi.ac.uk/efo/EFO_0021995 GCST90239020 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin-10 level in Chronic kidney disease with hypertension and no diabetes (8780_2) 466 African American individuals NA Illumina [14870897] (imputed) 2 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239021 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRCA1-A complex subunit Abraxas level in Chronic kidney disease with hypertension and no diabetes (8784_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRCA1-A complex subunit Abraxas 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044294 GCST90239022 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Armadillo repeat-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (8785_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239023 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM171B level in Chronic kidney disease with hypertension and no diabetes (8786_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239024 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arylsulfatase A level in Chronic kidney disease with hypertension and no diabetes (8790_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 arylsulfatase A measurement http://www.ebi.ac.uk/efo/EFO_0020163 GCST90239025 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 5A, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8791_151) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbonic anhydrase 5A, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040859 GCST90239026 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dipeptidase 1 level in Chronic kidney disease with hypertension and no diabetes (8794_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of dipeptidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041348 GCST90239027 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transferrin receptor protein 1 level in Chronic kidney disease with hypertension and no diabetes (8795_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239028 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 17 level in Chronic kidney disease with hypertension and no diabetes (8800_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239029 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nectin-1, isoform gamma level in Chronic kidney disease with hypertension and no diabetes (8803_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239030 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(XX) chain level in Chronic kidney disease with hypertension and no diabetes (8804_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(XX) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041084 GCST90239031 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-1 level in Chronic kidney disease with hypertension and no diabetes (8807_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043582 GCST90239032 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte cell adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (8810_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatocyte cell adhesion molecule in blood serum http://purl.obolibrary.org/obo/OBA_2041856 GCST90239033 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoic acid receptor responder protein 1 level in Chronic kidney disease with hypertension and no diabetes (8398_277) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of retinoic acid receptor responder protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043198 GCST90238934 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase 17B level in Chronic kidney disease with hypertension and no diabetes (8399_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase 17B measurement http://www.ebi.ac.uk/efo/EFO_0008281 GCST90238935 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastrin-releasing peptide level in Chronic kidney disease with hypertension and no diabetes (8400_74) 466 African American individuals NA Illumina [14870897] (imputed) 1 gastrin-releasing peptide measurement http://www.ebi.ac.uk/efo/EFO_0022000 GCST90238936 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid synthase level in Chronic kidney disease with hypertension and no diabetes (8403_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fatty acid synthase in blood serum http://purl.obolibrary.org/obo/OBA_2041550 GCST90238937 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BolA-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (8404_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BolA-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040817 GCST90238938 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (8405_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238939 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor I level in Chronic kidney disease with hypertension and no diabetes (8406_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-like growth factor I in blood serum http://purl.obolibrary.org/obo/OBA_2042067 GCST90238940 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurogenic locus notch homolog protein 2 level in Chronic kidney disease with hypertension and no diabetes (8407_84) 466 African American individuals NA Illumina [14870897] (imputed) 1 neurogenic locus notch homolog protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020599 GCST90238941 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. R-spondin-2 level in Chronic kidney disease with hypertension and no diabetes (8409_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 r-spondin-2 measurement http://www.ebi.ac.uk/efo/EFO_0020696 GCST90238942 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catenin beta-1 level in Chronic kidney disease with hypertension and no diabetes (8418_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of catenin beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040402 GCST90238943 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catenin beta-1 level in Chronic kidney disease with hypertension and no diabetes (8424_269) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of catenin beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040402 GCST90238944 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. R-spondin-3 level in Chronic kidney disease with hypertension and no diabetes (8427_118) 466 African American individuals NA Illumina [14870897] (imputed) 0 r-spondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0021878 GCST90238945 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurotrimin level in Chronic kidney disease with hypertension and no diabetes (8428_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurotrimin in blood serum http://purl.obolibrary.org/obo/OBA_2042654 GCST90238946 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Axin-2 level in Chronic kidney disease with hypertension and no diabetes (8429_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Axin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040741 GCST90238947 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pituitary adenylate cyclase-activating polypeptide 27 level in Chronic kidney disease with hypertension and no diabetes (8446_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 pituitary adenylate cyclase-activating polypeptide 27 measurement http://www.ebi.ac.uk/efo/EFO_0020640 GCST90238948 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Appetite-regulating hormone level in Chronic kidney disease with hypertension and no diabetes (8447_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 appetite-regulating hormone measurement http://www.ebi.ac.uk/efo/EFO_0022016 GCST90238949 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pituitary adenylate cyclase-activating polypeptide 38 level in Chronic kidney disease with hypertension and no diabetes (8450_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 pituitary adenylate cyclase-activating polypeptide 38 measurement http://www.ebi.ac.uk/efo/EFO_0020641 GCST90238950 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-synuclein level in Chronic kidney disease with hypertension and no diabetes (8458_111) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0009323 GCST90238951 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-synuclein level in Chronic kidney disease with hypertension and no diabetes (8458_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha synuclein measurement http://www.ebi.ac.uk/efo/EFO_0009323 GCST90238952 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone morphogenetic protein 6 level in Chronic kidney disease with hypertension and no diabetes (8459_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 bone morphogenetic protein 6 measurement http://www.ebi.ac.uk/efo/EFO_0020186 GCST90238953 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Somatotropin level in Chronic kidney disease with hypertension and no diabetes (8462_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 somatotropin measurement http://www.ebi.ac.uk/efo/EFO_0022017 GCST90238954 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Extracellular superoxide dismutase [Cu-Zn] level in Chronic kidney disease with hypertension and no diabetes (8463_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of extracellular superoxide dismutase [Cu-Zn] in blood serum http://purl.obolibrary.org/obo/OBA_2043596 GCST90238955 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. R-spondin-4 level in Chronic kidney disease with hypertension and no diabetes (8464_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 R-spondin-4 measurement http://www.ebi.ac.uk/efo/EFO_0022019 GCST90238956 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin H level in Chronic kidney disease with hypertension and no diabetes (8465_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 cathepsin H measurement http://www.ebi.ac.uk/efo/EFO_0020243 GCST90238957 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibin beta A chain:Inhibin beta B chain heterodimer level in Chronic kidney disease with hypertension and no diabetes (8467_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 inhibin beta A chain:inhibin beta B chain heterodimer measurement http://www.ebi.ac.uk/efo/EFO_0020470 GCST90238958 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 5 level in Chronic kidney disease with hypertension and no diabetes (9275_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sialic acid-binding Ig-like lectin 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040358 GCST90239284 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase A2 level in Chronic kidney disease with hypertension and no diabetes (9276_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase A2 in blood serum http://purl.obolibrary.org/obo/OBA_2041113 GCST90239285 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regenerating islet-derived protein 3-alpha level in Chronic kidney disease with hypertension and no diabetes (9277_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regenerating islet-derived protein 3-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043232 GCST90239286 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal cell-derived factor 1 level in Chronic kidney disease with hypertension and no diabetes (9278_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 stromal cell-derived factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020756 GCST90239287 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily member 11 level in Chronic kidney disease with hypertension and no diabetes (9279_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239288 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich secretory protein 2 level in Chronic kidney disease with hypertension and no diabetes (9282_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cysteine-rich secretory protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041144 GCST90239289 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD44 antigen level in Chronic kidney disease with hypertension and no diabetes (9283_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD44 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040262 GCST90239290 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted frizzled-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (9284_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secreted frizzled-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043476 GCST90239291 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sepiapterin reductase level in Chronic kidney disease with hypertension and no diabetes (9287_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sepiapterin reductase in blood serum http://purl.obolibrary.org/obo/OBA_2043643 GCST90239292 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase FKBP7 level in Chronic kidney disease with hypertension and no diabetes (9288_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of peptidyl-prolyl cis-trans isomerase FKBP7 in blood serum http://purl.obolibrary.org/obo/OBA_2041592 GCST90239293 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of microtubule dynamics protein 3 level in Chronic kidney disease with hypertension and no diabetes (9290_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of microtubule dynamics protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044353 GCST90239294 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microfibrillar-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (9294_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microfibrillar-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042349 GCST90239295 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-type tyrosine-protein phosphatase delta level in Chronic kidney disease with hypertension and no diabetes (9296_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-type tyrosine-protein phosphatase delta in blood serum http://purl.obolibrary.org/obo/OBA_2043105 GCST90239296 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 level in Chronic kidney disease with hypertension and no diabetes (9297_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040754 GCST90239297 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nectin-1, isoform gamma level in Chronic kidney disease with hypertension and no diabetes (9300_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239298 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth arrest and DNA damage-inducible proteins-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (9302_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of growth arrest and DNA damage-inducible proteins-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041652 GCST90239299 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ICOS ligand level in Chronic kidney disease with hypertension and no diabetes (9303_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 icos ligand measurement http://www.ebi.ac.uk/efo/EFO_0020460 GCST90239300 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon gamma receptor 2 level in Chronic kidney disease with hypertension and no diabetes (9305_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90239301 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 118 level in Chronic kidney disease with hypertension and no diabetes (9306_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of defensin beta 118 in blood serum http://purl.obolibrary.org/obo/OBA_2041276 GCST90239302 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD8 beta chain level in Chronic kidney disease with hypertension and no diabetes (9310_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of T-cell surface glycoprotein CD8 beta chain in blood serum http://purl.obolibrary.org/obo/OBA_2040239 GCST90239303 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc-alpha-2-glycoprotein level in Chronic kidney disease with hypertension and no diabetes (9312_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc-alpha-2-glycoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2040742 GCST90239304 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cerebellin-1 level in Chronic kidney disease with hypertension and no diabetes (9313_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cerebellin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040913 GCST90239305 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 5 level in Chronic kidney disease with hypertension and no diabetes (9314_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pregnancy-specific beta-1-glycoprotein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043060 GCST90239306 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial ubiquitin ligase activator of NFKB 1 level in Chronic kidney disease with hypertension and no diabetes (9315_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239307 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 1 level in Chronic kidney disease with hypertension and no diabetes (9316_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of WAP four-disulfide core domain protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044130 GCST90239308 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bile acid receptor level in Chronic kidney disease with hypertension and no diabetes (8946_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bile acid receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042630 GCST90239109 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 19 level in Chronic kidney disease with hypertension and no diabetes (8948_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 19 in blood serum http://purl.obolibrary.org/obo/OBA_2040496 GCST90239110 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-activated chloride channel regulator 2 level in Chronic kidney disease with hypertension and no diabetes (8950_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-activated chloride channel regulator 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041041 GCST90239111 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chondroitin sulfate proteoglycan 4 level in Chronic kidney disease with hypertension and no diabetes (8951_162) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chondroitin sulfate proteoglycan 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041174 GCST90239112 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granulocyte colony-stimulating factor level in Chronic kidney disease with hypertension and no diabetes (8952_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 granulocyte colony-stimulating factor measurement http://www.ebi.ac.uk/efo/EFO_0008142 GCST90239113 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatoma-derived growth factor level in Chronic kidney disease with hypertension and no diabetes (8953_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatoma-derived growth factor in blood serum http://purl.obolibrary.org/obo/OBA_2041849 GCST90239114 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase kinase kinase kinase 1 level in Chronic kidney disease with hypertension and no diabetes (8954_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase kinase kinase kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042289 GCST90239115 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycosyltransferase 8 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8955_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycosyltransferase 8 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044665 GCST90239116 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor class F member 2 level in Chronic kidney disease with hypertension and no diabetes (8956_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90239117 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum lectin 1 level in Chronic kidney disease with hypertension and no diabetes (8957_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoplasmic reticulum lectin 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044661 GCST90239118 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neural cell adhesion molecule L1-like protein level in Chronic kidney disease with hypertension and no diabetes (8958_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 neural cell adhesion molecule l1-like protein measurement http://www.ebi.ac.uk/efo/EFO_0020595 GCST90239119 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 17 level in Chronic kidney disease with hypertension and no diabetes (8959_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239120 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum aminopeptidase 2 level in Chronic kidney disease with hypertension and no diabetes (8960_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of endoplasmic reticulum aminopeptidase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041500 GCST90239121 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosomal protein S6 kinase beta-1 level in Chronic kidney disease with hypertension and no diabetes (8962_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosomal protein S6 kinase beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040200 GCST90239122 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle transport through interaction with t-SNAREs homolog 1B level in Chronic kidney disease with hypertension and no diabetes (8963_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle transport through interaction with t-SNAREs homolog 1B in blood serum http://purl.obolibrary.org/obo/OBA_2044119 GCST90239123 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 26 level in Chronic kidney disease with hypertension and no diabetes (8967_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 26 in blood serum http://purl.obolibrary.org/obo/OBA_2041386 GCST90239124 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Monocyte differentiation antigen CD14 level in Chronic kidney disease with hypertension and no diabetes (8969_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of CD14 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040350 GCST90239125 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-interacting serine/threonine-protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (8970_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-interacting serine/threonine-protein kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043276 GCST90239126 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexin-1 level in Chronic kidney disease with hypertension and no diabetes (8971_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of neurexin-1-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2044246 GCST90239127 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fc receptor-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (8973_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239128 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collagen alpha-1(XV) chain level in Chronic kidney disease with hypertension and no diabetes (8974_172) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of collagen alpha-1(XV) chain in blood serum http://purl.obolibrary.org/obo/OBA_2041083 GCST90239129 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell differentiation protein RCD1 homolog level in Chronic kidney disease with hypertension and no diabetes (8975_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CCR4-NOT transcription complex subunit 9 in blood serum http://purl.obolibrary.org/obo/OBA_2043340 GCST90239130 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4 N-acetylgalactosaminyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (8976_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,4 N-acetylgalactosaminyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040755 GCST90239131 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase kinase kinase kinase 3 level in Chronic kidney disease with hypertension and no diabetes (8978_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase kinase kinase kinase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042290 GCST90239132 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell surface glycoprotein CD200 receptor 2 level in Chronic kidney disease with hypertension and no diabetes (8980_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell surface glycoprotein CD200 receptor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040940 GCST90239133 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tissue factor pathway inhibitor 2 level in Chronic kidney disease with hypertension and no diabetes (9233_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tissue factor pathway inhibitor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043833 GCST90239259 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Twisted gastrulation protein homolog 1 level in Chronic kidney disease with hypertension and no diabetes (9234_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of twisted gastrulation protein homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043964 GCST90239260 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9235_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plexin domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044346 GCST90239261 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal-regulatory protein gamma level in Chronic kidney disease with hypertension and no diabetes (9241_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal-regulatory protein gamma in blood serum http://purl.obolibrary.org/obo/OBA_2043512 GCST90239262 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Betacellulin level in Chronic kidney disease with hypertension and no diabetes (9242_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 betacellulin measurement http://www.ebi.ac.uk/efo/EFO_0021883 GCST90239263 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysozyme g-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (9243_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysozyme g-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042250 GCST90239264 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Palmitoyl-protein thioesterase 1 level in Chronic kidney disease with hypertension and no diabetes (9244_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of palmitoyl-protein thioesterase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043014 GCST90239265 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DL4 level in Chronic kidney disease with hypertension and no diabetes (9245_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 killer cell immunoglobulin-like receptor 2DL4 measurement http://www.ebi.ac.uk/efo/EFO_0008197 GCST90239266 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myeloid-derived growth factor level in Chronic kidney disease with hypertension and no diabetes (9248_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myeloid-derived growth factor in blood serum http://purl.obolibrary.org/obo/OBA_2044808 GCST90239267 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 9 level in Chronic kidney disease with hypertension and no diabetes (9249_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239268 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil defensin 1 level in Chronic kidney disease with hypertension and no diabetes (9250_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neutrophil defensin 1 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044900 GCST90239269 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epididymis-specific alpha-mannosidase level in Chronic kidney disease with hypertension and no diabetes (9251_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of epididymis-specific alpha-mannosidase in blood serum http://purl.obolibrary.org/obo/OBA_2042278 GCST90239270 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histo-blood group ABO system transferase level in Chronic kidney disease with hypertension and no diabetes (9253_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of histo-blood group ABO system transferase in blood serum http://purl.obolibrary.org/obo/OBA_2040463 GCST90239271 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High affinity immunoglobulin epsilon receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (9254_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high affinity immunoglobulin epsilon receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041561 GCST90239272 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17C level in Chronic kidney disease with hypertension and no diabetes (9255_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-17C in blood serum http://purl.obolibrary.org/obo/OBA_2040247 GCST90239273 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal pentraxin-1 level in Chronic kidney disease with hypertension and no diabetes (9256_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuronal pentraxin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042622 GCST90239274 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translational activator of cytochrome c oxidase 1 level in Chronic kidney disease with hypertension and no diabetes (9257_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of translational activator of cytochrome c oxidase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044457 GCST90239275 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 21 level in Chronic kidney disease with hypertension and no diabetes (9259_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 21 measurement http://www.ebi.ac.uk/efo/EFO_0020810 GCST90239276 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-B receptor 6 level in Chronic kidney disease with hypertension and no diabetes (9261_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin type-b receptor 6 measurement http://www.ebi.ac.uk/efo/EFO_0020355 GCST90239277 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin O level in Chronic kidney disease with hypertension and no diabetes (9264_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cathepsin O in blood serum http://purl.obolibrary.org/obo/OBA_2041195 GCST90239278 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glioma pathogenesis-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (9265_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glioma pathogenesis-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041729 GCST90239279 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Triggering receptor expressed on myeloid cells 1 level in Chronic kidney disease with hypertension and no diabetes (9266_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of triggering receptor expressed on myeloid cells 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043926 GCST90239280 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase A4 level in Chronic kidney disease with hypertension and no diabetes (9267_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of carboxypeptidase A4 in blood serum http://purl.obolibrary.org/obo/OBA_2041114 GCST90239281 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biotinidase level in Chronic kidney disease with hypertension and no diabetes (9269_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of biotinidase in blood serum http://purl.obolibrary.org/obo/OBA_2040831 GCST90239282 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal interaction molecule 1 level in Chronic kidney disease with hypertension and no diabetes (9271_101) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239283 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Janus kinase and microtubule-interacting protein 3 level in Chronic kidney disease with hypertension and no diabetes (9068_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Janus kinase and microtubule-interacting protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042068 GCST90239184 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C17orf67 level in Chronic kidney disease with hypertension and no diabetes (9070_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C17orf67 in blood serum http://purl.obolibrary.org/obo/OBA_2044823 GCST90239185 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid hydroxylase domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (9074_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fatty acid hydroxylase domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044856 GCST90239186 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0258 protein KIAA1024 level in Chronic kidney disease with hypertension and no diabetes (9075_121) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of major intrinsically disordered Notch2-binding receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044880 GCST90239187 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proenkephalin-A level in Chronic kidney disease with hypertension and no diabetes (9076_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proenkephalin-A in blood serum http://purl.obolibrary.org/obo/OBA_2042846 GCST90239188 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mannosyl-oligosaccharide 1,2-alpha-mannosidase IB level in Chronic kidney disease with hypertension and no diabetes (9077_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mannosyl-oligosaccharide 1,2-alpha-mannosidase IB in blood serum http://purl.obolibrary.org/obo/OBA_2042275 GCST90239189 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1-syntrophin level in Chronic kidney disease with hypertension and no diabetes (9078_207) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1-syntrophin in blood serum http://purl.obolibrary.org/obo/OBA_2043580 GCST90239190 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc transporter 3 level in Chronic kidney disease with hypertension and no diabetes (9081_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable proton-coupled zinc antiporter SLC30A3 in blood serum http://purl.obolibrary.org/obo/OBA_2043533 GCST90239191 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein sel-1 homolog 2 level in Chronic kidney disease with hypertension and no diabetes (9082_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein sel-1 homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043422 GCST90239192 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type substrate 1 level in Chronic kidney disease with hypertension and no diabetes (9083_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein phosphatase non-receptor type substrate 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040362 GCST90239193 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mammaglobin-B level in Chronic kidney disease with hypertension and no diabetes (9086_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 mammaglobin-b measurement http://www.ebi.ac.uk/efo/EFO_0020552 GCST90239194 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NHL repeat-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (9087_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NHL repeat-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044406 GCST90239195 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctophilin-3 level in Chronic kidney disease with hypertension and no diabetes (9089_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of junctophilin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042075 GCST90239196 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-like protein 4 level in Chronic kidney disease with hypertension and no diabetes (9090_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239197 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (9092_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239198 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 4 member C level in Chronic kidney disease with hypertension and no diabetes (9094_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of C-type lectin domain family 4 member C in blood serum http://purl.obolibrary.org/obo/OBA_2040260 GCST90239199 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial fission regulator 1 level in Chronic kidney disease with hypertension and no diabetes (9095_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial fission regulator 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042447 GCST90239200 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphoid-restricted membrane protein level in Chronic kidney disease with hypertension and no diabetes (9096_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol 1,4,5-triphosphate receptor associated 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042227 GCST90239201 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0577 protein KIAA1324 level in Chronic kidney disease with hypertension and no diabetes (9097_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239202 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-5 level in Chronic kidney disease with hypertension and no diabetes (9099_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043755 GCST90239203 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C5orf46 level in Chronic kidney disease with hypertension and no diabetes (9100_32) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of uncharacterized protein C5orf46 in blood serum http://purl.obolibrary.org/obo/OBA_2044834 GCST90239204 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protrudin level in Chronic kidney disease with hypertension and no diabetes (9102_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239205 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LysM and putative peptidoglycan-binding domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (9106_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LysM and putative peptidoglycan-binding domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044474 GCST90239206 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Armadillo repeat-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (9107_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of armadillo repeat-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2040678 GCST90239207 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-17 level in Chronic kidney disease with hypertension and no diabetes (9110_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-17 in blood serum http://purl.obolibrary.org/obo/OBA_2043752 GCST90239208 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-glucuronosyltransferase 1-8 level in Chronic kidney disease with hypertension and no diabetes (8899_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UDP-glucuronosyltransferase 1A8 in blood serum http://purl.obolibrary.org/obo/OBA_2044025 GCST90239084 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neogenin level in Chronic kidney disease with hypertension and no diabetes (8900_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neogenin in blood serum http://purl.obolibrary.org/obo/OBA_2042560 GCST90239085 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein gamma level in Chronic kidney disease with hypertension and no diabetes (8901_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 14-3-3 protein gamma in blood serum http://purl.obolibrary.org/obo/OBA_2044166 GCST90239086 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-activated potassium channel subunit beta-3 level in Chronic kidney disease with hypertension and no diabetes (8905_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-activated potassium channel subunit beta-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042091 GCST90239087 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and transmembrane domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (8906_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and transmembrane domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044620 GCST90239088 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-glucuronosyltransferase 2A1 level in Chronic kidney disease with hypertension and no diabetes (8907_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of UDP-glucuronosyltransferase 2A1 in blood serum http://purl.obolibrary.org/obo/OBA_2044026 GCST90239089 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Potassium voltage-gated channel subfamily E regulatory beta subunit 5 level in Chronic kidney disease with hypertension and no diabetes (8908_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239090 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucosamine-6-phosphate isomerase 1 level in Chronic kidney disease with hypertension and no diabetes (8909_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glucosamine-6-phosphate isomerase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041756 GCST90239091 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 11 level in Chronic kidney disease with hypertension and no diabetes (8913_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239092 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stromal interaction molecule 1 level in Chronic kidney disease with hypertension and no diabetes (8916_32) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239093 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-tyrosine kinase 2-beta level in Chronic kidney disease with hypertension and no diabetes (8918_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239094 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyadenylate-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (8921_139) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyadenylate-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042737 GCST90239095 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane and coiled-coil domains protein 3 level in Chronic kidney disease with hypertension and no diabetes (8922_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239096 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 16 level in Chronic kidney disease with hypertension and no diabetes (8923_94) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 16 in blood serum http://purl.obolibrary.org/obo/OBA_2044557 GCST90239097 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuron-specific vesicular protein calcyon level in Chronic kidney disease with hypertension and no diabetes (8924_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuron-specific vesicular protein calcyon in blood serum http://purl.obolibrary.org/obo/OBA_2040881 GCST90239098 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonucleoside-diphosphate reductase subunit M2 B level in Chronic kidney disease with hypertension and no diabetes (8925_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonucleoside-diphosphate reductase subunit M2 B in blood serum http://purl.obolibrary.org/obo/OBA_2043348 GCST90239099 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C7orf73 level in Chronic kidney disease with hypertension and no diabetes (8927_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of short transmembrane mitochondrial protein 1 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044893 GCST90239100 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor TFIIIB component B'' homolog level in Chronic kidney disease with hypertension and no diabetes (8929_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor TFIIIB component B'' in blood serum http://purl.obolibrary.org/obo/OBA_2040791 GCST90239101 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G0/G1 switch protein 2 level in Chronic kidney disease with hypertension and no diabetes (8931_124) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of G0/G1 switch protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044578 GCST90239102 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleoside triphosphate diphosphohydrolase 6 level in Chronic kidney disease with hypertension and no diabetes (8932_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ectonucleoside triphosphate diphosphohydrolase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041484 GCST90239103 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myocyte-specific enhancer factor 2C level in Chronic kidney disease with hypertension and no diabetes (8933_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myocyte-specific enhancer factor 2C in blood serum http://purl.obolibrary.org/obo/OBA_2042330 GCST90239104 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Multidrug resistance-associated protein 6 level in Chronic kidney disease with hypertension and no diabetes (8935_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-binding cassette sub-family C member 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040457 GCST90239105 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-3 level in Chronic kidney disease with hypertension and no diabetes (8941_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroligin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042589 GCST90239106 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L21, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8942_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L21, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042426 GCST90239107 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRISC complex subunit Abro1 level in Chronic kidney disease with hypertension and no diabetes (8945_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRISC complex subunit Abraxas 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044537 GCST90239108 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 132 level in Chronic kidney disease with hypertension and no diabetes (9022_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 132 in blood serum http://purl.obolibrary.org/obo/OBA_2041283 GCST90239159 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin-like protein 8 level in Chronic kidney disease with hypertension and no diabetes (9026_40) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of butyrophilin-like protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040837 GCST90239160 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-2 level in Chronic kidney disease with hypertension and no diabetes (9027_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239161 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly(A) RNA polymerase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9028_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of poly(A) RNA polymerase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042455 GCST90239162 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C17orf89 level in Chronic kidney disease with hypertension and no diabetes (9030_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044812 GCST90239163 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proto-oncogene tyrosine-protein kinase ROS level in Chronic kidney disease with hypertension and no diabetes (9032_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proto-oncogene tyrosine-protein kinase ROS in blood serum http://purl.obolibrary.org/obo/OBA_2043312 GCST90239164 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAX-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (9035_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of max-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042470 GCST90239165 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-18 level in Chronic kidney disease with hypertension and no diabetes (9037_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-18 in blood serum http://purl.obolibrary.org/obo/OBA_2043711 GCST90239166 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein JTB level in Chronic kidney disease with hypertension and no diabetes (9038_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein JTB in blood serum http://purl.obolibrary.org/obo/OBA_2042077 GCST90239167 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Torsin-1A-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (9039_47) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239168 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mammalian ependymin-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (9040_144) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mammalian ependymin-related protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041488 GCST90239169 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Contactin-associated protein-like 5 level in Chronic kidney disease with hypertension and no diabetes (9044_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of contactin-associated protein-like 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041076 GCST90239170 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Very long-chain acyl-CoA synthetase level in Chronic kidney disease with hypertension and no diabetes (9045_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of long-chain fatty acid transport protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043532 GCST90239171 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Monocarboxylate transporter 4 level in Chronic kidney disease with hypertension and no diabetes (9049_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of monocarboxylate transporter 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043526 GCST90239172 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arginine/serine-rich protein 1 level in Chronic kidney disease with hypertension and no diabetes (9050_170) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arginine/serine-rich protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044865 GCST90239173 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-32 level in Chronic kidney disease with hypertension and no diabetes (9051_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-32 in blood serum http://purl.obolibrary.org/obo/OBA_2040290 GCST90239174 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich protein 2 level in Chronic kidney disease with hypertension and no diabetes (9053_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine-rich protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041142 GCST90239175 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myocardial zonula adherens protein level in Chronic kidney disease with hypertension and no diabetes (9055_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myocardial zonula adherens protein in blood serum http://purl.obolibrary.org/obo/OBA_2044333 GCST90239176 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasomal ubiquitin receptor ADRM1 level in Chronic kidney disease with hypertension and no diabetes (9057_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasomal ubiquitin receptor ADRM1 in blood serum http://purl.obolibrary.org/obo/OBA_2040526 GCST90239177 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit Tim21 level in Chronic kidney disease with hypertension and no diabetes (9058_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import inner membrane translocase subunit Tim21 in blood serum http://purl.obolibrary.org/obo/OBA_2044447 GCST90239178 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rap guanine nucleotide exchange factor 5 level in Chronic kidney disease with hypertension and no diabetes (9059_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rap guanine nucleotide exchange factor 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043197 GCST90239179 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein turtle homolog B level in Chronic kidney disease with hypertension and no diabetes (9060_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein turtle homolog B in blood serum http://purl.obolibrary.org/obo/OBA_2041997 GCST90239180 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho guanine nucleotide exchange factor 10 level in Chronic kidney disease with hypertension and no diabetes (9061_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho guanine nucleotide exchange factor 10 in blood serum http://purl.obolibrary.org/obo/OBA_2040658 GCST90239181 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 215 level in Chronic kidney disease with hypertension and no diabetes (9064_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239182 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-taxilin level in Chronic kidney disease with hypertension and no diabetes (9065_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-taxilin in blood serum http://purl.obolibrary.org/obo/OBA_2040265 GCST90239183 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin-3 level in Chronic kidney disease with hypertension and no diabetes (8982_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thrombospondin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2040203 GCST90239134 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Golgi membrane protein 1 level in Chronic kidney disease with hypertension and no diabetes (8983_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Golgi membrane protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041762 GCST90239135 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and calponin homology domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (8984_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239136 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein SERAC1 level in Chronic kidney disease with hypertension and no diabetes (8985_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein SERAC1 in blood serum http://purl.obolibrary.org/obo/OBA_2043454 GCST90239137 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. D-3-phosphoglycerate dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (8986_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of D-3-phosphoglycerate dehydrogenase in blood serum http://purl.obolibrary.org/obo/OBA_2042875 GCST90239138 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal peptide, CUB and EGF-like domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8989_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal peptide, CUB and EGF-like domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043410 GCST90239139 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 2 level in Chronic kidney disease with hypertension and no diabetes (8992_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell surface hyaluronidase in blood serum http://purl.obolibrary.org/obo/OBA_2044426 GCST90239140 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-interacting serine/threonine-protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (8993_151) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-interacting serine/threonine-protein kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043276 GCST90239141 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLAM family member 8 level in Chronic kidney disease with hypertension and no diabetes (8994_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLAM family member 8 in blood serum http://purl.obolibrary.org/obo/OBA_2043521 GCST90239142 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal pentraxin receptor level in Chronic kidney disease with hypertension and no diabetes (8997_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of neuronal pentraxin receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042624 GCST90239143 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan sulfate glucosamine 3-O-sulfotransferase 4 level in Chronic kidney disease with hypertension and no diabetes (8998_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heparan sulfate glucosamine 3-O-sulfotransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041933 GCST90239144 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 3 level in Chronic kidney disease with hypertension and no diabetes (8999_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040267 GCST90239145 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutral and basic amino acid transport protein rBAT level in Chronic kidney disease with hypertension and no diabetes (9000_177) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neutral and basic amino acid transport protein rBAT in blood serum http://purl.obolibrary.org/obo/OBA_2043535 GCST90239146 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin A11 level in Chronic kidney disease with hypertension and no diabetes (9002_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin A11 in blood serum http://purl.obolibrary.org/obo/OBA_2043456 GCST90239147 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage receptor MARCO level in Chronic kidney disease with hypertension and no diabetes (9003_99) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of macrophage receptor MARCO in blood serum http://purl.obolibrary.org/obo/OBA_2040348 GCST90239148 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor class A domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (9004_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor class A domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044799 GCST90239149 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin-A1 level in Chronic kidney disease with hypertension and no diabetes (9005_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plexin-A1 in blood serum http://purl.obolibrary.org/obo/OBA_2042937 GCST90239150 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane gamma-carboxyglutamic acid protein 1 level in Chronic kidney disease with hypertension and no diabetes (9008_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239151 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-mRNA-processing factor 6 level in Chronic kidney disease with hypertension and no diabetes (9012_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239152 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin-1 level in Chronic kidney disease with hypertension and no diabetes (9013_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 netrin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022009 GCST90239153 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 25 level in Chronic kidney disease with hypertension and no diabetes (9014_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 25 in blood serum http://purl.obolibrary.org/obo/OBA_2044416 GCST90239154 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteoglycan 3 level in Chronic kidney disease with hypertension and no diabetes (9015_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of proteoglycan 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043024 GCST90239155 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxysterols receptor LXR-beta level in Chronic kidney disease with hypertension and no diabetes (9016_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of oxysterols receptor LXR-beta in blood serum http://purl.obolibrary.org/obo/OBA_2042629 GCST90239156 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactase-phlorizin hydrolase level in Chronic kidney disease with hypertension and no diabetes (9017_58) 466 African American individuals NA Illumina [14870897] (imputed) 5 level of lactase/phlorizin hydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2042177 GCST90239157 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin-10 level in Chronic kidney disease with hypertension and no diabetes (9018_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239158 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 9 level in Chronic kidney disease with hypertension and no diabetes (9188_119) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-X-C motif chemokine 9 measurement http://www.ebi.ac.uk/efo/EFO_0022032 GCST90239234 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD63 antigen level in Chronic kidney disease with hypertension and no diabetes (9190_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD63 antigen measurement http://www.ebi.ac.uk/efo/EFO_0022033 GCST90239235 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trefoil factor 2 level in Chronic kidney disease with hypertension and no diabetes (9191_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 trefoil factor 2 measurement http://www.ebi.ac.uk/efo/EFO_0021846 GCST90239236 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-7 level in Chronic kidney disease with hypertension and no diabetes (9196_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-7 measurement http://www.ebi.ac.uk/efo/EFO_0022034 GCST90239237 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-9 level in Chronic kidney disease with hypertension and no diabetes (9197_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-9 measurement http://www.ebi.ac.uk/efo/EFO_0021863 GCST90239238 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 G2 level in Chronic kidney disease with hypertension and no diabetes (9199_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin-conjugating enzyme E2 G2 measurement http://www.ebi.ac.uk/efo/EFO_0022035 GCST90239239 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transgelin-2 level in Chronic kidney disease with hypertension and no diabetes (9201_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 transgelin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021884 GCST90239240 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP synthase subunit O, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9202_309) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP synthase subunit O, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040732 GCST90239241 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pro-opiomelanocortin level in Chronic kidney disease with hypertension and no diabetes (9204_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 pro-opiomelanocortin measurement http://www.ebi.ac.uk/efo/EFO_0022037 GCST90239242 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Quinone oxidoreductase-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (9207_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 quinone oxidoreductase-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021880 GCST90239243 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pigment epithelium-derived factor level in Chronic kidney disease with hypertension and no diabetes (9211_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 pigment epithelium-derived factor measurement http://www.ebi.ac.uk/efo/EFO_0021847 GCST90239244 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin F level in Chronic kidney disease with hypertension and no diabetes (9212_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin F measurement http://www.ebi.ac.uk/efo/EFO_0022038 GCST90239245 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 25 level in Chronic kidney disease with hypertension and no diabetes (9215_117) 466 African American individuals NA Illumina [14870897] (imputed) 0 ubiquitin carboxyl-terminal hydrolase 25 measurement http://www.ebi.ac.uk/efo/EFO_0021881 GCST90239246 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin-B2 level in Chronic kidney disease with hypertension and no diabetes (9216_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 plexin-B2 measurement http://www.ebi.ac.uk/efo/EFO_0021867 GCST90239247 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 6 level in Chronic kidney disease with hypertension and no diabetes (9218_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90239248 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neudesin level in Chronic kidney disease with hypertension and no diabetes (9219_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neudesin in blood serum http://purl.obolibrary.org/obo/OBA_2042559 GCST90239249 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-B receptor 3 level in Chronic kidney disease with hypertension and no diabetes (9220_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ephrin type-B receptor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041494 GCST90239250 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 level in Chronic kidney disease with hypertension and no diabetes (9221_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol 1,4,5-trisphosphate receptor-interacting protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042064 GCST90239251 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mesencephalic astrocyte-derived neurotrophic factor level in Chronic kidney disease with hypertension and no diabetes (9223_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein ARMET in blood serum http://purl.obolibrary.org/obo/OBA_2040679 GCST90239252 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolactin receptor level in Chronic kidney disease with hypertension and no diabetes (9224_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 prolactin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020656 GCST90239253 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane and ubiquitin-like domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (9226_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane and ubiquitin-like domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044629 GCST90239254 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death protein 1 level in Chronic kidney disease with hypertension and no diabetes (9227_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of programmed cell death protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040355 GCST90239255 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymotrypsin-like protease CTRL-1 level in Chronic kidney disease with hypertension and no diabetes (9229_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chymotrypsin-like protease CTRL-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041194 GCST90239256 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol monophosphatase 3 level in Chronic kidney disease with hypertension and no diabetes (9231_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Golgi-resident adenosine 3',5'-bisphosphate 3'-phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2042024 GCST90239257 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Roundabout homolog 4 level in Chronic kidney disease with hypertension and no diabetes (9232_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of roundabout homolog 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043306 GCST90239258 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Junctophilin-4 level in Chronic kidney disease with hypertension and no diabetes (9111_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of junctophilin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2042076 GCST90239209 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uromodulin-like 1 level in Chronic kidney disease with hypertension and no diabetes (9114_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uromodulin-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044032 GCST90239210 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADAM DEC1 level in Chronic kidney disease with hypertension and no diabetes (9115_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADAM DEC1 in blood serum http://purl.obolibrary.org/obo/OBA_2040504 GCST90239211 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HEPACAM family member 2 level in Chronic kidney disease with hypertension and no diabetes (9116_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239212 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-36 gamma level in Chronic kidney disease with hypertension and no diabetes (9117_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-1 family member 9 in blood serum http://purl.obolibrary.org/obo/OBA_2042007 GCST90239213 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galactoside 2-alpha-L-fucosyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (9121_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of galactoside alpha-(1,2)-fucosyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041634 GCST90239214 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Dos level in Chronic kidney disease with hypertension and no diabetes (9123_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-dependent calcium channel beta subunit-associated regulatory protein in blood serum http://purl.obolibrary.org/obo/OBA_2041345 GCST90239215 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mannan-binding lectin serine protease 1 level in Chronic kidney disease with hypertension and no diabetes (9125_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 mannan-binding lectin serine protease 1 measurement http://www.ebi.ac.uk/efo/EFO_0008223 GCST90239216 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5'-nucleotidase domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (9126_171) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5'-nucleotidase domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044647 GCST90239217 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prestin level in Chronic kidney disease with hypertension and no diabetes (9127_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prestin in blood serum http://purl.obolibrary.org/obo/OBA_2043530 GCST90239218 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane protein FLRT3 level in Chronic kidney disease with hypertension and no diabetes (9128_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine-rich repeat transmembrane protein FLRT3 measurement http://www.ebi.ac.uk/efo/EFO_0021861 GCST90239219 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 26 level in Chronic kidney disease with hypertension and no diabetes (9168_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 26 measurement http://www.ebi.ac.uk/efo/EFO_0022024 GCST90239220 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small ubiquitin-related modifier 3 level in Chronic kidney disease with hypertension and no diabetes (9169_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 small ubiquitin-related modifier 3 measurement http://www.ebi.ac.uk/efo/EFO_0022025 GCST90239221 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17A level in Chronic kidney disease with hypertension and no diabetes (9170_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17A measurement http://www.ebi.ac.uk/efo/EFO_0022026 GCST90239222 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine and glycine-rich protein 3 level in Chronic kidney disease with hypertension and no diabetes (9171_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 cysteine and glycine-rich protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0022027 GCST90239223 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil collagenase level in Chronic kidney disease with hypertension and no diabetes (9172_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 neutrophil collagenase measurement http://www.ebi.ac.uk/efo/EFO_0008248 GCST90239224 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoglucomutase-1 level in Chronic kidney disease with hypertension and no diabetes (9173_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 phosphoglucomutase-1 measurement http://www.ebi.ac.uk/efo/EFO_0021859 GCST90239225 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mucin-1 level in Chronic kidney disease with hypertension and no diabetes (9176_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 mucin-1 measurement http://www.ebi.ac.uk/efo/EFO_0021841 GCST90239226 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM3B level in Chronic kidney disease with hypertension and no diabetes (9177_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein FAM3B measurement http://www.ebi.ac.uk/efo/EFO_0021857 GCST90239227 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuregulin-1 level in Chronic kidney disease with hypertension and no diabetes (9178_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuregulin-1 measurement http://www.ebi.ac.uk/efo/EFO_0022029 GCST90239228 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon gamma receptor 2 level in Chronic kidney disease with hypertension and no diabetes (9180_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon gamma receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0022030 GCST90239229 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 1, soluble level in Chronic kidney disease with hypertension and no diabetes (9182_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239230 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha/beta receptor 1 level in Chronic kidney disease with hypertension and no diabetes (9183_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 interferon alpha/beta receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021850 GCST90239231 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trefoil factor 1 level in Chronic kidney disease with hypertension and no diabetes (9185_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 trefoil factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021865 GCST90239232 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Non-histone chromosomal protein HMG-14 level in Chronic kidney disease with hypertension and no diabetes (9187_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 non-histone chromosomal protein HMG-14 measurement http://www.ebi.ac.uk/efo/EFO_0021872 GCST90239233 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Iron-sulfur cluster assembly enzyme ISCU, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7201_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of iron-sulfur cluster assembly enzyme ISCU in blood serum http://purl.obolibrary.org/obo/OBA_2042042 GCST90238541 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-6C level in Chronic kidney disease with hypertension and no diabetes (7202_107) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-6C in blood serum http://purl.obolibrary.org/obo/OBA_2043436 GCST90238542 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-N-acetylglucosaminyltransferase radical fringe level in Chronic kidney disease with hypertension and no diabetes (7203_125) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of beta-1,3-N-acetylglucosaminyltransferase radical fringe in blood serum http://purl.obolibrary.org/obo/OBA_2043247 GCST90238543 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 21 level in Chronic kidney disease with hypertension and no diabetes (7204_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 21 in blood serum http://purl.obolibrary.org/obo/OBA_2040979 GCST90238544 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fructose-1,6-bisphosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (7206_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fructose-1,6-bisphosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041555 GCST90238545 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Red level in Chronic kidney disease with hypertension and no diabetes (7207_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Red in blood serum http://purl.obolibrary.org/obo/OBA_2041999 GCST90238546 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C level in Chronic kidney disease with hypertension and no diabetes (7208_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C in blood serum http://purl.obolibrary.org/obo/OBA_2042361 GCST90238547 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (7210_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of amyloid beta precursor like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040617 GCST90238548 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease pancreatic level in Chronic kidney disease with hypertension and no diabetes (7211_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonuclease pancreatic in blood serum http://purl.obolibrary.org/obo/OBA_2043280 GCST90238549 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH-cytochrome b5 reductase 3 level in Chronic kidney disease with hypertension and no diabetes (7215_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH-cytochrome b5 reductase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041212 GCST90238550 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium/potassium-transporting ATPase subunit beta-2 level in Chronic kidney disease with hypertension and no diabetes (7218_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium/potassium-transporting ATPase subunit beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040726 GCST90238551 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1A level in Chronic kidney disease with hypertension and no diabetes (7219_152) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock 70 kDa protein 1A measurement http://www.ebi.ac.uk/efo/EFO_0021975 GCST90238552 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoskeleton-associated protein 4 level in Chronic kidney disease with hypertension and no diabetes (7221_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytoskeleton-associated protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041036 GCST90238553 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A13 level in Chronic kidney disease with hypertension and no diabetes (7223_60) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein S100-A13 in blood serum http://purl.obolibrary.org/obo/OBA_2043364 GCST90238554 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell receptor-associated transmembrane adapter 1 level in Chronic kidney disease with hypertension and no diabetes (7224_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-cell receptor-associated transmembrane adapter 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043924 GCST90238555 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane magnesium transporter 1 level in Chronic kidney disease with hypertension and no diabetes (7225_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ER membrane protein complex subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042386 GCST90238556 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cochlin level in Chronic kidney disease with hypertension and no diabetes (7227_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cochlin in blood serum http://purl.obolibrary.org/obo/OBA_2041078 GCST90238557 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 level in Chronic kidney disease with hypertension and no diabetes (7228_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043680 GCST90238558 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protease serine 11A level in Chronic kidney disease with hypertension and no diabetes (7231_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protease serine 11A in blood serum http://purl.obolibrary.org/obo/OBA_2043881 GCST90238559 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. P2X purinoceptor 6 level in Chronic kidney disease with hypertension and no diabetes (7233_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of P2X purinoceptor 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042730 GCST90238560 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Procollagen galactosyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (7234_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of procollagen galactosyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044424 GCST90238561 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase Mu 1 level in Chronic kidney disease with hypertension and no diabetes (7239_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase mu 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041806 GCST90238562 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane-bound transcription factor site-1 protease level in Chronic kidney disease with hypertension and no diabetes (7240_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane-bound transcription factor site-1 protease in blood serum http://purl.obolibrary.org/obo/OBA_2042311 GCST90238563 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and transmembrane domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (7242_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-set and transmembrane domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044610 GCST90238564 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon beta level in Chronic kidney disease with hypertension and no diabetes (7243_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon beta 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041983 GCST90238565 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zona pellucida sperm-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (7766_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zona pellucida sperm-binding protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044217 GCST90238616 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase M level in Chronic kidney disease with hypertension and no diabetes (7768_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of carboxypeptidase M in blood serum http://purl.obolibrary.org/obo/OBA_2041120 GCST90238617 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NFU1 iron-sulfur cluster scaffold homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7770_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NFU1 iron-sulfur cluster scaffold, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042574 GCST90238618 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DL2 level in Chronic kidney disease with hypertension and no diabetes (7773_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of killer cell immunoglobulin-like receptor 2DL2 in blood serum http://purl.obolibrary.org/obo/OBA_2042104 GCST90238619 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-11 level in Chronic kidney disease with hypertension and no diabetes (7775_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 kallikrein-11 measurement http://www.ebi.ac.uk/efo/EFO_0010573 GCST90238620 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5B level in Chronic kidney disease with hypertension and no diabetes (7776_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of netrin receptor UNC5B in blood serum http://purl.obolibrary.org/obo/OBA_2044038 GCST90238621 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase recruitment domain-containing protein 19 level in Chronic kidney disease with hypertension and no diabetes (7778_104) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caspase recruitment domain-containing protein 19 in blood serum http://purl.obolibrary.org/obo/OBA_2044858 GCST90238622 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 11 level in Chronic kidney disease with hypertension and no diabetes (7779_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 11 in blood serum http://purl.obolibrary.org/obo/OBA_2041021 GCST90238623 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Marginal zone B- and B1-cell-specific protein level in Chronic kidney disease with hypertension and no diabetes (7780_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proapoptotic caspase adapter protein in blood serum http://purl.obolibrary.org/obo/OBA_2042738 GCST90238624 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epididymal secretory protein E3-beta level in Chronic kidney disease with hypertension and no diabetes (7782_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epididymal secretory protein E3-beta in blood serum http://purl.obolibrary.org/obo/OBA_2044660 GCST90238625 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kininogen-1 level in Chronic kidney disease with hypertension and no diabetes (7784_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 kininogen-1 measurement http://www.ebi.ac.uk/efo/EFO_0008198 GCST90238626 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 2 member B level in Chronic kidney disease with hypertension and no diabetes (7786_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 2 member B in blood serum http://purl.obolibrary.org/obo/OBA_2044662 GCST90238627 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily A member 5 level in Chronic kidney disease with hypertension and no diabetes (7787_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of leukocyte immunoglobulin-like receptor subfamily A member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042197 GCST90238628 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP synthase-coupling factor 6, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7788_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP synthase-coupling factor 6, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040730 GCST90238629 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxiredoxin-4 level in Chronic kidney disease with hypertension and no diabetes (7789_182) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxiredoxin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043021 GCST90238630 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukemia inhibitory factor level in Chronic kidney disease with hypertension and no diabetes (7790_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukemia inhibitory factor in blood serum http://purl.obolibrary.org/obo/OBA_2042193 GCST90238631 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 90B, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7792_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of coiled-coil domain-containing protein 90B, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044259 GCST90238632 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2-E type II integral membrane protein level in Chronic kidney disease with hypertension and no diabetes (7795_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238633 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell antigen receptor complex-associated protein alpha chain level in Chronic kidney disease with hypertension and no diabetes (7796_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell antigen receptor complex-associated protein alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2040257 GCST90238634 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 167 level in Chronic kidney disease with hypertension and no diabetes (7797_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 167 in blood serum http://purl.obolibrary.org/obo/OBA_2044722 GCST90238635 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DL5A level in Chronic kidney disease with hypertension and no diabetes (7799_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of killer cell immunoglobulin-like receptor 2DL5A in blood serum http://purl.obolibrary.org/obo/OBA_2042106 GCST90238636 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (7803_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041019 GCST90238637 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Golgi SNAP receptor complex member 1 level in Chronic kidney disease with hypertension and no diabetes (7805_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Golgi SNAP receptor complex member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041766 GCST90238638 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4-galactosyltransferase 7 level in Chronic kidney disease with hypertension and no diabetes (7806_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,4-galactosyltransferase 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040761 GCST90238639 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. D-glucuronyl C5-epimerase level in Chronic kidney disease with hypertension and no diabetes (7808_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of D-glucuronyl C5-epimerase in blood serum http://purl.obolibrary.org/obo/OBA_2041727 GCST90238640 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uromodulin level in Chronic kidney disease with hypertension and no diabetes (9451_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 uromodulin measurement http://www.ebi.ac.uk/efo/EFO_0021778 GCST90239359 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vascular endothelial growth factor B level in Chronic kidney disease with hypertension and no diabetes (9453_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vascular endothelial growth factor B in blood serum http://purl.obolibrary.org/obo/OBA_2040414 GCST90239360 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-22 receptor subunit alpha-2 level in Chronic kidney disease with hypertension and no diabetes (9456_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-22 receptor subunit alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0020500 GCST90239361 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caveolin-2 level in Chronic kidney disease with hypertension and no diabetes (9457_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caveolin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040908 GCST90239362 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 6 level in Chronic kidney disease with hypertension and no diabetes (9459_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90239363 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 4 level in Chronic kidney disease with hypertension and no diabetes (9461_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of intercellular adhesion molecule 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040277 GCST90239364 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicular integral-membrane protein VIP36 level in Chronic kidney disease with hypertension and no diabetes (9468_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 vesicular integral-membrane protein VIP36 measurement http://www.ebi.ac.uk/efo/EFO_0022012 GCST90239365 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methyltransferase-like protein 24 level in Chronic kidney disease with hypertension and no diabetes (9470_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable methyltransferase-like protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2044602 GCST90239366 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Asialoglycoprotein receptor 2 level in Chronic kidney disease with hypertension and no diabetes (9474_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of asialoglycoprotein receptor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040698 GCST90239367 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epididymal secretory glutathione peroxidase level in Chronic kidney disease with hypertension and no diabetes (9475_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epididymal secretory glutathione peroxidase in blood serum http://purl.obolibrary.org/obo/OBA_2041780 GCST90239368 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoribosyl pyrophosphate synthase-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (9478_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoribosyl pyrophosphate synthase-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043041 GCST90239369 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribose pyrophosphatase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9482_110) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ADP-ribose pyrophosphatase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042674 GCST90239370 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Desmoglein-2 level in Chronic kidney disease with hypertension and no diabetes (9484_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 desmoglein-2 measurement http://www.ebi.ac.uk/efo/EFO_0020322 GCST90239371 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 125 level in Chronic kidney disease with hypertension and no diabetes (9486_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 125 in blood serum http://purl.obolibrary.org/obo/OBA_2041279 GCST90239372 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Somatoliberin level in Chronic kidney disease with hypertension and no diabetes (9487_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of somatoliberin in blood serum http://purl.obolibrary.org/obo/OBA_2041715 GCST90239373 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C4orf32 level in Chronic kidney disease with hypertension and no diabetes (9490_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein FAM241A in blood serum http://purl.obolibrary.org/obo/OBA_2044844 GCST90239374 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 17 level in Chronic kidney disease with hypertension and no diabetes (9495_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-X-C motif chemokine 17 in blood serum http://purl.obolibrary.org/obo/OBA_2040328 GCST90239375 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuromedin-S level in Chronic kidney disease with hypertension and no diabetes (9503_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuromedin-S in blood serum http://purl.obolibrary.org/obo/OBA_2042600 GCST90239376 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-27A level in Chronic kidney disease with hypertension and no diabetes (9504_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-27A in blood serum http://purl.obolibrary.org/obo/OBA_2043149 GCST90239377 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein L1 level in Chronic kidney disease with hypertension and no diabetes (9506_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 apolipoprotein L1 measurement http://www.ebi.ac.uk/efo/EFO_0021854 GCST90239378 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trimeric intracellular cation channel type B level in Chronic kidney disease with hypertension and no diabetes (9509_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of trimeric intracellular cation channel type B in blood serum http://purl.obolibrary.org/obo/OBA_2043873 GCST90239379 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexophilin-2 level in Chronic kidney disease with hypertension and no diabetes (9511_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurexophilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042682 GCST90239380 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 22 level in Chronic kidney disease with hypertension and no diabetes (9513_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor 22 in blood serum http://purl.obolibrary.org/obo/OBA_2041573 GCST90239381 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EF-hand calcium-binding domain-containing protein 14 level in Chronic kidney disease with hypertension and no diabetes (9514_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239382 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phospholipase A1 member A level in Chronic kidney disease with hypertension and no diabetes (9518_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipase A1 member A in blood serum http://purl.obolibrary.org/obo/OBA_2042910 GCST90239383 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystic fibrosis transmembrane conductance regulator level in Chronic kidney disease with hypertension and no diabetes (7717_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cystic fibrosis transmembrane conductance regulator in blood serum http://purl.obolibrary.org/obo/OBA_2040236 GCST90238591 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fragile X mental retardation protein 1 level in Chronic kidney disease with hypertension and no diabetes (7721_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fragile X messenger ribonucleoprotein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040440 GCST90238592 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-associated membrane protein 4 level in Chronic kidney disease with hypertension and no diabetes (7732_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-associated membrane protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044077 GCST90238593 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pigment epithelium-derived factor level in Chronic kidney disease with hypertension and no diabetes (7735_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 pigment epithelium-derived factor measurement http://www.ebi.ac.uk/efo/EFO_0021847 GCST90238594 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin beta-6 level in Chronic kidney disease with hypertension and no diabetes (7737_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin beta-6 in blood serum http://purl.obolibrary.org/obo/OBA_2042053 GCST90238595 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-2 level in Chronic kidney disease with hypertension and no diabetes (7738_299) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043713 GCST90238596 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fetal and adult testis-expressed transcript protein level in Chronic kidney disease with hypertension and no diabetes (7740_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fetal and adult testis-expressed transcript protein in blood serum http://purl.obolibrary.org/obo/OBA_2041551 GCST90238597 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA polymerase-associated protein RTF1 homolog level in Chronic kidney disease with hypertension and no diabetes (7741_111) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA polymerase-associated protein RTF1 in blood serum http://purl.obolibrary.org/obo/OBA_2043351 GCST90238598 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 148 level in Chronic kidney disease with hypertension and no diabetes (7742_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238599 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit TIM50 level in Chronic kidney disease with hypertension and no diabetes (7743_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import inner membrane translocase subunit TIM50 in blood serum http://purl.obolibrary.org/obo/OBA_2043855 GCST90238600 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 12 level in Chronic kidney disease with hypertension and no diabetes (7744_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of low-density lipoprotein receptor-related protein 12 in blood serum http://purl.obolibrary.org/obo/OBA_2042230 GCST90238601 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CDGSH iron-sulfur domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (7745_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CDGSH iron-sulfur domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041034 GCST90238602 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7747_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 11, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042544 GCST90238603 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7748_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042547 GCST90238604 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted frizzled-related protein 2 level in Chronic kidney disease with hypertension and no diabetes (7751_121) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secreted frizzled-related protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043475 GCST90238605 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 4 member D level in Chronic kidney disease with hypertension and no diabetes (7752_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 4 member D in blood serum http://purl.obolibrary.org/obo/OBA_2041047 GCST90238606 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxidoreductase HTATIP2 level in Chronic kidney disease with hypertension and no diabetes (7753_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of oxidoreductase HTATIP2 in blood serum http://purl.obolibrary.org/obo/OBA_2041956 GCST90238607 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein jagged-1 level in Chronic kidney disease with hypertension and no diabetes (7754_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein jagged-1 measurement http://www.ebi.ac.uk/efo/EFO_0008271 GCST90238608 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin beta-5 level in Chronic kidney disease with hypertension and no diabetes (7755_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin beta-5 in blood serum http://purl.obolibrary.org/obo/OBA_2042052 GCST90238609 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell lectin-like receptor subfamily F member 1 level in Chronic kidney disease with hypertension and no diabetes (7756_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 killer cell lectin-like receptor subfamily F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020520 GCST90238610 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HLA class II histocompatibility antigen, DQ alpha 2 chain level in Chronic kidney disease with hypertension and no diabetes (7757_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MHC class II histocompatibility antigen alpha chain DQA2 in blood serum http://purl.obolibrary.org/obo/OBA_2040364 GCST90238611 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 215 level in Chronic kidney disease with hypertension and no diabetes (7758_217) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238612 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Choline/ethanolamine kinase level in Chronic kidney disease with hypertension and no diabetes (7761_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 choline/ethanolamine kinase measurement http://www.ebi.ac.uk/efo/EFO_0021935 GCST90238613 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-11 level in Chronic kidney disease with hypertension and no diabetes (7763_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238614 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integral membrane protein 2A level in Chronic kidney disease with hypertension and no diabetes (7765_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integral membrane protein 2A in blood serum http://purl.obolibrary.org/obo/OBA_2044777 GCST90238615 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kit ligand level in Chronic kidney disease with hypertension and no diabetes (9377_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 kit ligand measurement http://www.ebi.ac.uk/efo/EFO_0010612 GCST90239334 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibrinogen C domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9378_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibrinogen C domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044795 GCST90239335 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small integral membrane protein 10 level in Chronic kidney disease with hypertension and no diabetes (9379_248) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of small integral membrane protein 10 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044919 GCST90239336 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Group XIIB secretory phospholipase A2-like protein level in Chronic kidney disease with hypertension and no diabetes (9380_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of group XIIB secretory phospholipase A2-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042912 GCST90239337 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chitinase-3-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (9383_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chitinase-3-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041006 GCST90239338 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathelicidin antimicrobial peptide level in Chronic kidney disease with hypertension and no diabetes (9384_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cathelicidin antimicrobial peptide in blood serum http://purl.obolibrary.org/obo/OBA_2044228 GCST90239339 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 9B level in Chronic kidney disease with hypertension and no diabetes (9386_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tetratricopeptide repeat protein 9B in blood serum http://purl.obolibrary.org/obo/OBA_2044723 GCST90239340 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methylmalonyl-CoA epimerase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9388_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methylmalonyl-CoA epimerase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042312 GCST90239341 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ProSAAS level in Chronic kidney disease with hypertension and no diabetes (9391_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ProSAAS in blood serum http://purl.obolibrary.org/obo/OBA_2042806 GCST90239342 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A level in Chronic kidney disease with hypertension and no diabetes (9392_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A in blood serum http://purl.obolibrary.org/obo/OBA_2042359 GCST90239343 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase Q level in Chronic kidney disease with hypertension and no diabetes (9394_19) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of carboxypeptidase Q in blood serum http://purl.obolibrary.org/obo/OBA_2042859 GCST90239344 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galanin-like peptide level in Chronic kidney disease with hypertension and no diabetes (9398_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of galanin-like peptide in blood serum http://purl.obolibrary.org/obo/OBA_2041668 GCST90239345 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-7 level in Chronic kidney disease with hypertension and no diabetes (9400_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-7 measurement http://www.ebi.ac.uk/efo/EFO_0022034 GCST90239346 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metalloprotease TIKI1 level in Chronic kidney disease with hypertension and no diabetes (9401_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of metalloprotease TIKI1 in blood serum http://purl.obolibrary.org/obo/OBA_2044516 GCST90239347 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Discoidin, CUB and LCCL domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9402_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of discoidin, CUB and LCCL domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044468 GCST90239348 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptase beta-1 level in Chronic kidney disease with hypertension and no diabetes (9409_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tryptase alpha/beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044575 GCST90239349 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activin receptor type-2B level in Chronic kidney disease with hypertension and no diabetes (9412_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activin receptor type-2B in blood serum http://purl.obolibrary.org/obo/OBA_2040190 GCST90239350 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase M level in Chronic kidney disease with hypertension and no diabetes (9416_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase M in blood serum http://purl.obolibrary.org/obo/OBA_2041120 GCST90239351 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-binding protein inhibitor ID-2 level in Chronic kidney disease with hypertension and no diabetes (9426_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-binding protein inhibitor ID-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040187 GCST90239352 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-binding protein inhibitor ID-1 level in Chronic kidney disease with hypertension and no diabetes (9436_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-binding protein inhibitor ID-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040186 GCST90239353 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin K level in Chronic kidney disease with hypertension and no diabetes (9443_137) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cathepsin K in blood serum http://purl.obolibrary.org/obo/OBA_2040338 GCST90239354 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein DGCR6 level in Chronic kidney disease with hypertension and no diabetes (9444_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein DGCR6 in blood serum http://purl.obolibrary.org/obo/OBA_2041292 GCST90239355 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C19orf18 level in Chronic kidney disease with hypertension and no diabetes (9445_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C19orf18 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044913 GCST90239356 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C4b-binding protein alpha chain level in Chronic kidney disease with hypertension and no diabetes (9449_150) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C4b-binding protein alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2044425 GCST90239357 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 2-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (9450_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 2-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040966 GCST90239358 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 25 level in Chronic kidney disease with hypertension and no diabetes (9317_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239309 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane emp24 domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (9319_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane emp24 domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043869 GCST90239310 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuromedin-B level in Chronic kidney disease with hypertension and no diabetes (9321_400) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuromedin-B in blood serum http://purl.obolibrary.org/obo/OBA_2042594 GCST90239311 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inter-alpha-trypsin inhibitor heavy chain H2 level in Chronic kidney disease with hypertension and no diabetes (9326_33) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of inter-alpha-trypsin inhibitor heavy chain H2 in blood serum http://purl.obolibrary.org/obo/OBA_2042057 GCST90239312 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ly6/PLAUR domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9327_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ly6/PLAUR domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044783 GCST90239313 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trem-like transcript 1 protein level in Chronic kidney disease with hypertension and no diabetes (9329_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239314 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 136 level in Chronic kidney disease with hypertension and no diabetes (9332_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of defensin beta 136 in blood serum http://purl.obolibrary.org/obo/OBA_2041285 GCST90239315 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endoplasmic reticulum resident protein 27 level in Chronic kidney disease with hypertension and no diabetes (9333_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endoplasmic reticulum resident protein 27 in blood serum http://purl.obolibrary.org/obo/OBA_2041510 GCST90239316 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protachykinin-1 level in Chronic kidney disease with hypertension and no diabetes (9337_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protachykinin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043763 GCST90239317 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase FKBP14 level in Chronic kidney disease with hypertension and no diabetes (9340_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase FKBP14 in blood serum http://purl.obolibrary.org/obo/OBA_2041586 GCST90239318 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor D level in Chronic kidney disease with hypertension and no diabetes (9341_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of platelet-derived growth factor D in blood serum http://purl.obolibrary.org/obo/OBA_2040219 GCST90239319 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-2 receptor subunit beta level in Chronic kidney disease with hypertension and no diabetes (9343_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-2 receptor subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040287 GCST90239320 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 13 level in Chronic kidney disease with hypertension and no diabetes (9345_436) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein WFDC13 in blood serum http://purl.obolibrary.org/obo/OBA_2044133 GCST90239321 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1r subcomponent-like protein level in Chronic kidney disease with hypertension and no diabetes (9348_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1r subcomponent-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2040854 GCST90239322 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follistatin-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (9350_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of follistatin-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041622 GCST90239323 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein CREG1 level in Chronic kidney disease with hypertension and no diabetes (9357_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein CREG1 in blood serum http://purl.obolibrary.org/obo/OBA_2041137 GCST90239324 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein delta homolog 2 level in Chronic kidney disease with hypertension and no diabetes (9359_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein delta homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041314 GCST90239325 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EGF-like repeat and discoidin I-like domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (9360_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EGF-like repeat and discoidin I-like domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041412 GCST90239326 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin alpha-C2 level in Chronic kidney disease with hypertension and no diabetes (9361_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin alpha-C2 in blood serum http://purl.obolibrary.org/obo/OBA_2042788 GCST90239327 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cancer/testis antigen 55 level in Chronic kidney disease with hypertension and no diabetes (9363_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cancer/testis antigen 55 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044916 GCST90239328 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein eyes shut homolog level in Chronic kidney disease with hypertension and no diabetes (9365_91) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein eyes shut in blood serum http://purl.obolibrary.org/obo/OBA_2041424 GCST90239329 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and transmembrane domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9368_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and transmembrane domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044329 GCST90239330 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 4C level in Chronic kidney disease with hypertension and no diabetes (9369_174) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of netrin-G1 ligand in blood serum http://purl.obolibrary.org/obo/OBA_2042236 GCST90239331 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-glutamyl hydrolase level in Chronic kidney disease with hypertension and no diabetes (9370_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-glutamyl hydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2041710 GCST90239332 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myelin protein zero-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (9372_157) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myelin protein zero-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042411 GCST90239333 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. IGF-like family receptor 1 level in Chronic kidney disease with hypertension and no diabetes (7244_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of IGF-like family receptor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044420 GCST90238566 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUGBP Elav-like family member 2 level in Chronic kidney disease with hypertension and no diabetes (7245_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CUGBP Elav-like family member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041197 GCST90238567 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FRAS1-related extracellular matrix protein 2 level in Chronic kidney disease with hypertension and no diabetes (7246_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of FRAS1-related extracellular matrix protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041616 GCST90238568 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RAB6-interacting golgin level in Chronic kidney disease with hypertension and no diabetes (7247_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RAB6-interacting golgin in blood serum http://purl.obolibrary.org/obo/OBA_2041765 GCST90238569 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bcl-2-like protein 10 level in Chronic kidney disease with hypertension and no diabetes (7249_307) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Bcl-2-like protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2040789 GCST90238570 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q tumor necrosis factor-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (7251_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q tumor necrosis factor-related protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040850 GCST90238571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein quaking level in Chronic kidney disease with hypertension and no diabetes (7253_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of KH domain-containing RNA-binding protein QKI in blood serum http://purl.obolibrary.org/obo/OBA_2043130 GCST90238572 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bone marrow proteoglycan level in Chronic kidney disease with hypertension and no diabetes (7258_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bone marrow proteoglycan in blood serum http://purl.obolibrary.org/obo/OBA_2043023 GCST90238573 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 14 level in Chronic kidney disease with hypertension and no diabetes (7262_191) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 14 in blood serum http://purl.obolibrary.org/obo/OBA_2041023 GCST90238574 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteocrin level in Chronic kidney disease with hypertension and no diabetes (7265_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of osteocrin in blood serum http://purl.obolibrary.org/obo/OBA_2042718 GCST90238575 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin A9 level in Chronic kidney disease with hypertension and no diabetes (7266_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin A9 in blood serum http://purl.obolibrary.org/obo/OBA_2043457 GCST90238576 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine palmitoyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (7267_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine palmitoyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043648 GCST90238577 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-4 level in Chronic kidney disease with hypertension and no diabetes (7268_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041979 GCST90238578 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 32 level in Chronic kidney disease with hypertension and no diabetes (7551_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transforming growth factor beta activator LRRC32 in blood serum http://purl.obolibrary.org/obo/OBA_2044526 GCST90238579 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin-2 level in Chronic kidney disease with hypertension and no diabetes (7624_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 ankyrin-2 measurement http://www.ebi.ac.uk/efo/EFO_0021874 GCST90238580 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 14-3-3 protein theta level in Chronic kidney disease with hypertension and no diabetes (7625_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 14-3-3 protein theta measurement http://www.ebi.ac.uk/efo/EFO_0022011 GCST90238581 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich with EGF-like domain protein 1 level in Chronic kidney disease with hypertension and no diabetes (7628_40) 466 African American individuals NA Illumina [14870897] (imputed) 1 cysteine-rich with EGF-like domain protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021870 GCST90238582 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicular integral-membrane protein VIP36 level in Chronic kidney disease with hypertension and no diabetes (7638_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 vesicular integral-membrane protein VIP36 measurement http://www.ebi.ac.uk/efo/EFO_0022012 GCST90238583 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin-binding protein C, slow-type level in Chronic kidney disease with hypertension and no diabetes (7648_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin-binding protein C, slow-type in blood serum http://purl.obolibrary.org/obo/OBA_2042473 GCST90238584 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-terminal pro-BNP level in Chronic kidney disease with hypertension and no diabetes (7655_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 N-terminal pro-BNP measurement http://www.ebi.ac.uk/efo/EFO_0022014 GCST90238585 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomyosin alpha-4 chain level in Chronic kidney disease with hypertension and no diabetes (7660_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 tropomyosin alpha-4 chain measurement http://www.ebi.ac.uk/efo/EFO_0022015 GCST90238586 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 10B level in Chronic kidney disease with hypertension and no diabetes (7693_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 10B measurement http://www.ebi.ac.uk/efo/EFO_0021993 GCST90238587 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Next to BRCA1 gene 1 protein level in Chronic kidney disease with hypertension and no diabetes (7696_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of next to BRCA1 gene 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042519 GCST90238588 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fragile X mental retardation protein 1 level in Chronic kidney disease with hypertension and no diabetes (7713_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fragile X messenger ribonucleoprotein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040440 GCST90238589 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fragile X mental retardation protein 1 level in Chronic kidney disease with hypertension and no diabetes (7713_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fragile X messenger ribonucleoprotein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040440 GCST90238590 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Laminin subunit gamma-2 level in Chronic kidney disease with hypertension and no diabetes (9580_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of laminin subunit gamma-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042160 GCST90239409 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-mRNA-processing factor 6 level in Chronic kidney disease with hypertension and no diabetes (9581_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239410 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (7174_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021923 GCST90238518 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin gamma-A2 level in Chronic kidney disease with hypertension and no diabetes (7175_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin gamma-A2 in blood serum http://purl.obolibrary.org/obo/OBA_2042795 GCST90238519 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein DEPP level in Chronic kidney disease with hypertension and no diabetes (7178_59) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein DEPP1 in blood serum http://purl.obolibrary.org/obo/OBA_2041287 GCST90238520 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurofascin level in Chronic kidney disease with hypertension and no diabetes (7179_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurofascin in blood serum http://purl.obolibrary.org/obo/OBA_2042568 GCST90238521 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-14 level in Chronic kidney disease with hypertension and no diabetes (7180_114) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-14 in blood serum http://purl.obolibrary.org/obo/OBA_2041976 GCST90238522 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-associated membrane protein-associated protein B/C level in Chronic kidney disease with hypertension and no diabetes (7181_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-associated membrane protein-associated protein B/C in blood serum http://purl.obolibrary.org/obo/OBA_2044377 GCST90238523 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Liver carboxylesterase 1 level in Chronic kidney disease with hypertension and no diabetes (7182_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of liver carboxylesterase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040989 GCST90238524 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-like protein 8 level in Chronic kidney disease with hypertension and no diabetes (7183_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of angiopoietin-like protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2044836 GCST90238525 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carcinoembryonic antigen-related cell adhesion molecule 7 level in Chronic kidney disease with hypertension and no diabetes (7184_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carcinoembryonic antigen-related cell adhesion molecule 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040981 GCST90238526 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet glycoprotein V level in Chronic kidney disease with hypertension and no diabetes (7185_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of platelet glycoprotein V in blood serum http://purl.obolibrary.org/obo/OBA_2040354 GCST90238527 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-3 level in Chronic kidney disease with hypertension and no diabetes (7186_111) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043714 GCST90238528 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1L level in Chronic kidney disease with hypertension and no diabetes (7187_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1L in blood serum http://purl.obolibrary.org/obo/OBA_2042996 GCST90238529 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbohydrate sulfotransferase 3 level in Chronic kidney disease with hypertension and no diabetes (7189_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbohydrate sulfotransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041024 GCST90238530 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 4 level in Chronic kidney disease with hypertension and no diabetes (7190_50) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ephrin type-A receptor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041489 GCST90238531 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon lambda receptor 1 level in Chronic kidney disease with hypertension and no diabetes (7192_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-28 receptor alpha chain in blood serum http://purl.obolibrary.org/obo/OBA_2042015 GCST90238532 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin alpha-C1 level in Chronic kidney disease with hypertension and no diabetes (7193_98) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin alpha-C1 in blood serum http://purl.obolibrary.org/obo/OBA_2042787 GCST90238533 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroplastin level in Chronic kidney disease with hypertension and no diabetes (7194_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroplastin in blood serum http://purl.obolibrary.org/obo/OBA_2042621 GCST90238534 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin type-A receptor 7 level in Chronic kidney disease with hypertension and no diabetes (7195_119) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ephrin type-A receptor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041491 GCST90238535 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon omega-1 level in Chronic kidney disease with hypertension and no diabetes (7196_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon omega-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041985 GCST90238536 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 15 level in Chronic kidney disease with hypertension and no diabetes (7197_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 15 in blood serum http://purl.obolibrary.org/obo/OBA_2044282 GCST90238537 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycosaminoglycan xylosylkinase level in Chronic kidney disease with hypertension and no diabetes (7198_197) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycosaminoglycan xylosylkinase in blood serum http://purl.obolibrary.org/obo/OBA_2044245 GCST90238538 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synapsin-3 level in Chronic kidney disease with hypertension and no diabetes (7199_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synapsin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043744 GCST90238539 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and fibronectin type-III domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (7200_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and fibronectin type-III domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044458 GCST90238540 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apoptosis-inducing factor 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9522_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apoptosis-inducing factor 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040542 GCST90239384 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integral membrane protein 2C level in Chronic kidney disease with hypertension and no diabetes (9523_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239385 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative spermatogenesis-associated protein 31D4 level in Chronic kidney disease with hypertension and no diabetes (9524_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spermatogenesis-associated protein 31D4 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044908 GCST90239386 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive tyrosine-protein kinase 7 level in Chronic kidney disease with hypertension and no diabetes (9525_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inactive tyrosine-protein kinase 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043096 GCST90239387 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Colipase-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (9526_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of colipase-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044720 GCST90239388 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte-specific transcript 1 protein level in Chronic kidney disease with hypertension and no diabetes (9531_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukocyte-specific transcript 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2042245 GCST90239389 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WW domain binding protein 1-like level in Chronic kidney disease with hypertension and no diabetes (9532_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WW domain binding protein 1-like in blood serum http://purl.obolibrary.org/obo/OBA_2044559 GCST90239390 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epididymal secretory protein E3-alpha level in Chronic kidney disease with hypertension and no diabetes (9536_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epididymal secretory protein E3-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2044784 GCST90239391 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-galactosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (9541_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-galactosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040745 GCST90239392 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Conserved oligomeric Golgi complex subunit 8 level in Chronic kidney disease with hypertension and no diabetes (9543_131) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of conserved oligomeric Golgi complex subunit 8 in blood serum http://purl.obolibrary.org/obo/OBA_2041079 GCST90239393 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C7orf69 level in Chronic kidney disease with hypertension and no diabetes (9544_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239394 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granzyme K level in Chronic kidney disease with hypertension and no diabetes (9545_156) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of granzyme K in blood serum http://purl.obolibrary.org/obo/OBA_2040447 GCST90239395 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EMI domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9547_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EMI domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044780 GCST90239396 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 17 level in Chronic kidney disease with hypertension and no diabetes (9550_153) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239397 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MANSC domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9557_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MANSC domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044739 GCST90239398 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Versican core protein level in Chronic kidney disease with hypertension and no diabetes (9561_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of versican core protein in blood serum http://purl.obolibrary.org/obo/OBA_2044088 GCST90239399 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PRKC apoptosis WT1 regulator protein level in Chronic kidney disease with hypertension and no diabetes (9565_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PRKC apoptosis WT1 regulator protein in blood serum http://purl.obolibrary.org/obo/OBA_2042768 GCST90239400 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High affinity immunoglobulin alpha and immunoglobulin mu Fc receptor level in Chronic kidney disease with hypertension and no diabetes (9568_289) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high affinity immunoglobulin alpha and immunoglobulin mu Fc receptor in blood serum http://purl.obolibrary.org/obo/OBA_2041560 GCST90239401 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor class A member 3 level in Chronic kidney disease with hypertension and no diabetes (9569_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239402 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin domain-containing protein 11 level in Chronic kidney disease with hypertension and no diabetes (9573_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239403 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myc box-dependent-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (9574_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Myc box-dependent-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040798 GCST90239404 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Motor neuron and pancreas homeobox protein 1 level in Chronic kidney disease with hypertension and no diabetes (9576_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of motor neuron and pancreas homeobox protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042393 GCST90239405 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-2 level in Chronic kidney disease with hypertension and no diabetes (9577_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043753 GCST90239406 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MANSC domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (9578_263) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MANSC domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044763 GCST90239407 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane gamma-carboxyglutamic acid protein 4 level in Chronic kidney disease with hypertension and no diabetes (9579_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane gamma-carboxyglutamic acid protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043045 GCST90239408 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein WFDC11 level in Chronic kidney disease with hypertension and no diabetes (7969_163) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein WFDC11 in blood serum http://purl.obolibrary.org/obo/OBA_2044132 GCST90238741 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ecto-ADP-ribosyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (7970_315) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ecto-ADP-ribosyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040394 GCST90238742 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5A level in Chronic kidney disease with hypertension and no diabetes (7975_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of netrin receptor UNC5A in blood serum http://purl.obolibrary.org/obo/OBA_2044037 GCST90238743 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DOMON domain-containing protein FRRS1L level in Chronic kidney disease with hypertension and no diabetes (7976_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DOMON domain-containing protein FRRS1L in blood serum http://purl.obolibrary.org/obo/OBA_2044395 GCST90238744 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (7980_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040751 GCST90238745 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-galactosyltransferase 6 level in Chronic kidney disease with hypertension and no diabetes (7981_230) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-galactosyltransferase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040748 GCST90238746 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L32, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7982_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L32, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042428 GCST90238747 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin gamma-C5 level in Chronic kidney disease with hypertension and no diabetes (7983_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin gamma-C5 in blood serum http://purl.obolibrary.org/obo/OBA_2042798 GCST90238748 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylated-alpha-linked acidic dipeptidase 2 level in Chronic kidney disease with hypertension and no diabetes (7986_98) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetylated-alpha-linked acidic dipeptidase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042495 GCST90238749 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C1orf226 level in Chronic kidney disease with hypertension and no diabetes (7989_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C1orf226 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044892 GCST90238750 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Astacin-like metalloendopeptidase level in Chronic kidney disease with hypertension and no diabetes (7993_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of astacin-like metalloendopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2040709 GCST90238751 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ERO1-like protein beta level in Chronic kidney disease with hypertension and no diabetes (7994_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ERO1-like protein beta in blood serum http://purl.obolibrary.org/obo/OBA_2041509 GCST90238752 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. von Willebrand factor C domain-containing protein 2-like level in Chronic kidney disease with hypertension and no diabetes (7995_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of von Willebrand factor C domain-containing protein 2-like in blood serum http://purl.obolibrary.org/obo/OBA_2044576 GCST90238753 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Double C2-like domain-containing protein beta level in Chronic kidney disease with hypertension and no diabetes (7997_118) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of double C2-like domain-containing protein beta in blood serum http://purl.obolibrary.org/obo/OBA_2041339 GCST90238754 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleoside triphosphate diphosphohydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (7999_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 ectonucleoside triphosphate diphosphohydrolase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020342 GCST90238755 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 2DL5A level in Chronic kidney disease with hypertension and no diabetes (8000_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of killer cell immunoglobulin-like receptor 2DL5A in blood serum http://purl.obolibrary.org/obo/OBA_2042106 GCST90238756 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protease serine 5 level in Chronic kidney disease with hypertension and no diabetes (8002_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protease serine 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043884 GCST90238757 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat LGI family member 3 level in Chronic kidney disease with hypertension and no diabetes (8003_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat LGI family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044527 GCST90238758 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glyceraldehyde-3-phosphate dehydrogenase, testis-specific level in Chronic kidney disease with hypertension and no diabetes (8004_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glyceraldehyde-3-phosphate dehydrogenase, testis-specific in blood serum http://purl.obolibrary.org/obo/OBA_2041671 GCST90238759 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix-remodeling-associated protein 7 level in Chronic kidney disease with hypertension and no diabetes (8005_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of matrix-remodeling-associated protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042471 GCST90238760 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 12 level in Chronic kidney disease with hypertension and no diabetes (8006_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 12 in blood serum http://purl.obolibrary.org/obo/OBA_2044533 GCST90238761 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin B level in Chronic kidney disease with hypertension and no diabetes (8007_19) 466 African American individuals NA Illumina [14870897] (imputed) 1 cathepsin B measurement http://www.ebi.ac.uk/efo/EFO_0008072 GCST90238762 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activator of apoptosis harakiri level in Chronic kidney disease with hypertension and no diabetes (8008_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activator of apoptosis harakiri in blood serum http://purl.obolibrary.org/obo/OBA_2041927 GCST90238763 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Surfeit locus protein 1 level in Chronic kidney disease with hypertension and no diabetes (8009_121) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of surfeit locus protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043737 GCST90238764 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Iron/zinc purple acid phosphatase-like protein level in Chronic kidney disease with hypertension and no diabetes (8011_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acid phosphatase type 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042757 GCST90238765 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermatogenesis-associated protein 9 level in Chronic kidney disease with hypertension and no diabetes (7809_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spermatogenesis-associated protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2043620 GCST90238641 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C1q tumor necrosis factor-related protein 5 level in Chronic kidney disease with hypertension and no diabetes (7810_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of complement C1q tumor necrosis factor-related protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040852 GCST90238642 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A9 level in Chronic kidney disease with hypertension and no diabetes (7812_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein s100-a9 measurement http://www.ebi.ac.uk/efo/EFO_0020687 GCST90238643 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alkaline phosphatase, placental type level in Chronic kidney disease with hypertension and no diabetes (7813_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alkaline phosphatase, placental type in blood serum http://purl.obolibrary.org/obo/OBA_2040576 GCST90238644 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like growth factor-binding protein-like 1 level in Chronic kidney disease with hypertension and no diabetes (7815_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-like growth factor-binding protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041991 GCST90238645 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylate-binding protein 6 level in Chronic kidney disease with hypertension and no diabetes (7818_101) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanylate-binding protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041683 GCST90238646 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear nucleic acid-binding protein C1D level in Chronic kidney disease with hypertension and no diabetes (7821_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear nucleic acid-binding protein C1D in blood serum http://purl.obolibrary.org/obo/OBA_2040842 GCST90238647 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HRAS-like suppressor 2 level in Chronic kidney disease with hypertension and no diabetes (7822_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipase A and acyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041924 GCST90238648 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (7823_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043676 GCST90238649 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionine-R-sulfoxide reductase B3 level in Chronic kidney disease with hypertension and no diabetes (7824_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methionine-R-sulfoxide reductase B3, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042444 GCST90238650 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Monoacylglycerol lipase ABHD12 level in Chronic kidney disease with hypertension and no diabetes (7825_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysophosphatidylserine lipase ABHD12 in blood serum http://purl.obolibrary.org/obo/OBA_2044737 GCST90238651 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase DCLK3 level in Chronic kidney disease with hypertension and no diabetes (7826_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase DCLK3 in blood serum http://purl.obolibrary.org/obo/OBA_2041241 GCST90238652 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 32 level in Chronic kidney disease with hypertension and no diabetes (7827_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 32 in blood serum http://purl.obolibrary.org/obo/OBA_2040502 GCST90238653 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (7831_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 retinol-binding protein 4 measurement http://www.ebi.ac.uk/efo/EFO_0020707 GCST90238654 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase A3 level in Chronic kidney disease with hypertension and no diabetes (7832_181) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein disulfide-isomerase a3 measurement http://www.ebi.ac.uk/efo/EFO_0020668 GCST90238655 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BCL2/adenovirus E1B 19 kDa protein-interacting protein 3-like level in Chronic kidney disease with hypertension and no diabetes (7835_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BCL2/adenovirus E1B 19 kDa protein-interacting protein 3-like in blood serum http://purl.obolibrary.org/obo/OBA_2040815 GCST90238656 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Submaxillary gland androgen-regulated protein 3A level in Chronic kidney disease with hypertension and no diabetes (7838_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of submaxillary gland androgen-regulated protein 3A in blood serum http://purl.obolibrary.org/obo/OBA_2043559 GCST90238657 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM19A3 level in Chronic kidney disease with hypertension and no diabetes (7839_99) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chemokine-like protein TAFA-3 in blood serum http://purl.obolibrary.org/obo/OBA_2044738 GCST90238658 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Legumain level in Chronic kidney disease with hypertension and no diabetes (7840_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 legumain measurement http://www.ebi.ac.uk/efo/EFO_0020530 GCST90238659 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelial cell-selective adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (7841_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 endothelial cell-selective adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0008120 GCST90238660 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small EDRK-rich factor 1 level in Chronic kidney disease with hypertension and no diabetes (7842_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small EDRK-rich factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043762 GCST90238661 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 11 level in Chronic kidney disease with hypertension and no diabetes (7846_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pregnancy-specific beta-1-glycoprotein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2043056 GCST90238662 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaminyl-peptide cyclotransferase level in Chronic kidney disease with hypertension and no diabetes (7849_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutaminyl-peptide cyclotransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043131 GCST90238663 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase subunit 4 isoform 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7850_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome c oxidase subunit 4 isoform 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041105 GCST90238664 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 46 level in Chronic kidney disease with hypertension and no diabetes (7851_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 46 in blood serum http://purl.obolibrary.org/obo/OBA_2044508 GCST90238665 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translation initiation factor IF-3, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7852_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of translation initiation factor IF-3, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042451 GCST90238666 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein SCO1 homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7853_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein SCO1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043407 GCST90238667 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Natural cytotoxicity triggering receptor 3 ligand 1 level in Chronic kidney disease with hypertension and no diabetes (7854_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of natural cytotoxicity triggering receptor 3 ligand 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044482 GCST90238668 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM151A level in Chronic kidney disease with hypertension and no diabetes (7856_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM151A in blood serum http://purl.obolibrary.org/obo/OBA_2044688 GCST90238669 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurotensin/neuromedin N level in Chronic kidney disease with hypertension and no diabetes (7857_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurotensin/neuromedin N in blood serum http://purl.obolibrary.org/obo/OBA_2042656 GCST90238670 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin gamma-C3 level in Chronic kidney disease with hypertension and no diabetes (7859_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protocadherin gamma-C3 in blood serum http://purl.obolibrary.org/obo/OBA_2042797 GCST90238671 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable E3 ubiquitin-protein ligase HERC4 level in Chronic kidney disease with hypertension and no diabetes (7860_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of probable E3 ubiquitin-protein ligase HERC4 in blood serum http://purl.obolibrary.org/obo/OBA_2044752 GCST90238672 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase transmembrane receptor ROR2 level in Chronic kidney disease with hypertension and no diabetes (7861_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein kinase transmembrane receptor ROR2 in blood serum http://purl.obolibrary.org/obo/OBA_2043310 GCST90238673 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane-associated progesterone receptor component 1 level in Chronic kidney disease with hypertension and no diabetes (7863_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane-associated progesterone receptor component 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042869 GCST90238674 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 8 level in Chronic kidney disease with hypertension and no diabetes (7864_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sialic acid-binding Ig-like lectin 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040359 GCST90238675 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HRAS-like suppressor 3 level in Chronic kidney disease with hypertension and no diabetes (7865_126) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phospholipase A and acyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041925 GCST90238676 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 30 level in Chronic kidney disease with hypertension and no diabetes (7866_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of DnaJ homolog subfamily C member 30, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044390 GCST90238677 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (7867_154) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043675 GCST90238678 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-Ala-His dipeptidase level in Chronic kidney disease with hypertension and no diabetes (7870_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 beta-Ala-His dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0008033 GCST90238679 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 132A level in Chronic kidney disease with hypertension and no diabetes (7871_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transmembrane protein 132A in blood serum http://purl.obolibrary.org/obo/OBA_2043871 GCST90238680 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testis-specific serine/threonine-protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (7873_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of testis-specific serine/threonine-protein kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043953 GCST90238681 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin level in Chronic kidney disease with hypertension and no diabetes (7875_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin in blood serum http://purl.obolibrary.org/obo/OBA_2042925 GCST90238682 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein transport protein Sec61 subunit beta level in Chronic kidney disease with hypertension and no diabetes (7878_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein transport protein Sec61 subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2043420 GCST90238683 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome P450 3A4 level in Chronic kidney disease with hypertension and no diabetes (7879_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 cytochrome p450 3a4 measurement http://www.ebi.ac.uk/efo/EFO_0020303 GCST90238684 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-1 level in Chronic kidney disease with hypertension and no diabetes (7880_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 proteasome subunit alpha type-1 measurement http://www.ebi.ac.uk/efo/EFO_0020663 GCST90238685 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mono [ADP-ribose] polymerase PARP16 level in Chronic kidney disease with hypertension and no diabetes (7881_244) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein mono-ADP-ribosyltransferase PARP16 in blood serum http://purl.obolibrary.org/obo/OBA_2042764 GCST90238686 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLAM family member 7 level in Chronic kidney disease with hypertension and no diabetes (7882_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90238687 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine palmitoyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (7886_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine palmitoyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043647 GCST90238688 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase subunit 5B, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7887_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome c oxidase subunit 5B, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041108 GCST90238689 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase assembly factor 3 homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (7888_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 56 in blood serum http://purl.obolibrary.org/obo/OBA_2044263 GCST90238690 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-tyrosine sulfotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (7928_183) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-tyrosine sulfotransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043917 GCST90238716 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Exosome complex component CSL4 level in Chronic kidney disease with hypertension and no diabetes (7930_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of exosome complex component CSL4 in blood serum http://purl.obolibrary.org/obo/OBA_2041525 GCST90238717 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-8 level in Chronic kidney disease with hypertension and no diabetes (7932_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-8 in blood serum http://purl.obolibrary.org/obo/OBA_2043758 GCST90238718 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 22 level in Chronic kidney disease with hypertension and no diabetes (7933_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disintegrin and metalloproteinase domain-containing protein 22 in blood serum http://purl.obolibrary.org/obo/OBA_2040497 GCST90238719 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein NDRG4 level in Chronic kidney disease with hypertension and no diabetes (7934_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein NDRG4 in blood serum http://purl.obolibrary.org/obo/OBA_2042538 GCST90238720 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycosyltransferase-like protein LARGE1 level in Chronic kidney disease with hypertension and no diabetes (7935_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of xylosyl- and glucuronyltransferase LARGE1 in blood serum http://purl.obolibrary.org/obo/OBA_2042164 GCST90238721 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative uncharacterized protein PQLC2L level in Chronic kidney disease with hypertension and no diabetes (7939_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative uncharacterized protein SLC66A1L (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044890 GCST90238722 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUB and zona pellucida-like domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (7943_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CUB and zona pellucida-like domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041203 GCST90238723 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 3DL3 level in Chronic kidney disease with hypertension and no diabetes (7944_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238724 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-6A level in Chronic kidney disease with hypertension and no diabetes (7945_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90238725 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-4 complex accessory subunit tepsin level in Chronic kidney disease with hypertension and no diabetes (7947_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-4 complex accessory subunit Tepsin in blood serum http://purl.obolibrary.org/obo/OBA_2044634 GCST90238726 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycolipid transfer protein domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (7948_129) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glycolipid transfer protein domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044788 GCST90238727 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Butyrophilin-like protein 9 level in Chronic kidney disease with hypertension and no diabetes (7950_142) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of butyrophilin-like protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2040838 GCST90238728 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fc receptor-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (7951_146) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fc receptor-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041564 GCST90238729 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle transport through interaction with t-SNAREs homolog 1A level in Chronic kidney disease with hypertension and no diabetes (7952_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle transport through interaction with t-SNAREs homolog 1A in blood serum http://purl.obolibrary.org/obo/OBA_2044118 GCST90238730 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signaling lymphocytic activation molecule level in Chronic kidney disease with hypertension and no diabetes (7953_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLAM family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040333 GCST90238731 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inter-alpha-trypsin inhibitor heavy chain H1 level in Chronic kidney disease with hypertension and no diabetes (7955_195) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of inter-alpha-trypsin inhibitor heavy chain H1 in blood serum http://purl.obolibrary.org/obo/OBA_2042056 GCST90238732 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MICOS complex subunit MIC10 level in Chronic kidney disease with hypertension and no diabetes (7956_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MICOS complex subunit MIC10 in blood serum http://purl.obolibrary.org/obo/OBA_2044682 GCST90238733 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secretogranin-3 level in Chronic kidney disease with hypertension and no diabetes (7957_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of secretogranin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043395 GCST90238734 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kin of IRRE-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (7958_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kin of IRRE-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042111 GCST90238735 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-7 level in Chronic kidney disease with hypertension and no diabetes (7959_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-7 in blood serum http://purl.obolibrary.org/obo/OBA_2040964 GCST90238736 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. POTE ankyrin domain family member G level in Chronic kidney disease with hypertension and no diabetes (7960_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of POTE ankyrin domain family member G in blood serum http://purl.obolibrary.org/obo/OBA_2044580 GCST90238737 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 8 level in Chronic kidney disease with hypertension and no diabetes (7962_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine protease inhibitor Kazal-type 8 in blood serum http://purl.obolibrary.org/obo/OBA_2043636 GCST90238738 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemoglobin subunit theta-1 level in Chronic kidney disease with hypertension and no diabetes (7965_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of hemoglobin subunit theta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041842 GCST90238739 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytotoxic and regulatory T-cell molecule level in Chronic kidney disease with hypertension and no diabetes (7968_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 cytotoxic and regulatory t-cell molecule measurement http://www.ebi.ac.uk/efo/EFO_0020311 GCST90238740 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PILR alpha-associated neural protein level in Chronic kidney disease with hypertension and no diabetes (9599_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 PILR alpha-associated neural protein measurement http://www.ebi.ac.uk/efo/EFO_0021941 GCST90239418 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin type-1 domain-containing protein 7A level in Chronic kidney disease with hypertension and no diabetes (9600_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239419 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-22 receptor subunit alpha-1 level in Chronic kidney disease with hypertension and no diabetes (9603_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-22 receptor subunit alpha-1 measurement http://www.ebi.ac.uk/efo/EFO_0020499 GCST90239420 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-11 level in Chronic kidney disease with hypertension and no diabetes (9604_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239421 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear pore membrane glycoprotein 210-like level in Chronic kidney disease with hypertension and no diabetes (9606_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear pore membrane glycoprotein 210-like in blood serum http://purl.obolibrary.org/obo/OBA_2042677 GCST90239422 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proline-rich protein 27 level in Chronic kidney disease with hypertension and no diabetes (9607_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proline-rich protein 27 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044905 GCST90239423 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 275 level in Chronic kidney disease with hypertension and no diabetes (9609_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 275 in blood serum http://purl.obolibrary.org/obo/OBA_2044198 GCST90239424 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitrin level in Chronic kidney disease with hypertension and no diabetes (9627_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vitrin in blood serum http://purl.obolibrary.org/obo/OBA_2044102 GCST90239425 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell immunoreceptor with Ig and ITIM domains level in Chronic kidney disease with hypertension and no diabetes (9638_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T cell immunoreceptor with Ig and ITIM domains in blood serum http://purl.obolibrary.org/obo/OBA_2043850 GCST90239426 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor receptor-like protein level in Chronic kidney disease with hypertension and no diabetes (9713_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of platelet-derived growth factor receptor-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042825 GCST90239427 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily member 3 level in Chronic kidney disease with hypertension and no diabetes (9715_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin superfamily member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044563 GCST90239428 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-16 level in Chronic kidney disease with hypertension and no diabetes (9719_145) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrix metalloproteinase-16 measurement http://www.ebi.ac.uk/efo/EFO_0020559 GCST90239429 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Multimerin-2 level in Chronic kidney disease with hypertension and no diabetes (9723_105) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of multimerin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042391 GCST90239430 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase CCNB1IP1 level in Chronic kidney disease with hypertension and no diabetes (9728_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase CCNB1IP1 in blood serum http://purl.obolibrary.org/obo/OBA_2040933 GCST90239431 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GH3 domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (9730_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GH3 domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2044644 GCST90239432 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface protein tactile level in Chronic kidney disease with hypertension and no diabetes (9735_44) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of T-cell surface protein tactile in blood serum http://purl.obolibrary.org/obo/OBA_2040335 GCST90239433 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FAS-associated factor 2 level in Chronic kidney disease with hypertension and no diabetes (9738_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of FAS-associated factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041541 GCST90239434 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA mismatch repair protein Msh2 level in Chronic kidney disease with hypertension and no diabetes (9739_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA mismatch repair protein Msh2 in blood serum http://purl.obolibrary.org/obo/OBA_2042439 GCST90239435 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spliceosome RNA helicase DDX39B level in Chronic kidney disease with hypertension and no diabetes (9742_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spliceosome RNA helicase BAT1 in blood serum http://purl.obolibrary.org/obo/OBA_2040779 GCST90239436 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily A member 4 level in Chronic kidney disease with hypertension and no diabetes (9744_139) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily A member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044284 GCST90239437 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4E type 2 level in Chronic kidney disease with hypertension and no diabetes (9745_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 4E type 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041453 GCST90239438 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAP/microtubule affinity-regulating kinase 3 level in Chronic kidney disease with hypertension and no diabetes (9747_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MAP/microtubule affinity-regulating kinase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042300 GCST90239439 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase Mu 3 level in Chronic kidney disease with hypertension and no diabetes (9748_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase mu 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044306 GCST90239440 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plastin-2 level in Chronic kidney disease with hypertension and no diabetes (9749_190) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plastin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042176 GCST90239441 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A4 level in Chronic kidney disease with hypertension and no diabetes (9750_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein S100-A4 measurement http://www.ebi.ac.uk/efo/EFO_0021893 GCST90239442 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. VIP36-like protein level in Chronic kidney disease with hypertension and no diabetes (8013_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of VIP36-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042211 GCST90238766 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycoprotein endo-alpha-1,2-mannosidase level in Chronic kidney disease with hypertension and no diabetes (8014_359) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glycoprotein endo-alpha-1,2-mannosidase in blood serum http://purl.obolibrary.org/obo/OBA_2042280 GCST90238767 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 4 level in Chronic kidney disease with hypertension and no diabetes (8016_19) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238768 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FAD-dependent oxidoreductase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8017_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of FAD-dependent oxidoreductase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044641 GCST90238769 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and immunoglobulin domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (8018_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of V-set and immunoglobulin domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044774 GCST90238770 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Stathmin-3 level in Chronic kidney disease with hypertension and no diabetes (8019_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of stathmin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043703 GCST90238771 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L14, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8021_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L14, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042424 GCST90238772 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-tyrosine sulfotransferase 2 level in Chronic kidney disease with hypertension and no diabetes (8024_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-tyrosine sulfotransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043918 GCST90238773 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 5 level in Chronic kidney disease with hypertension and no diabetes (8028_22) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine protease inhibitor Kazal-type 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043632 GCST90238774 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial coiled-coil domain protein 1 level in Chronic kidney disease with hypertension and no diabetes (8032_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial coiled-coil domain protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044414 GCST90238775 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 18 level in Chronic kidney disease with hypertension and no diabetes (8033_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 18 in blood serum http://purl.obolibrary.org/obo/OBA_2044798 GCST90238776 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dorsal root ganglia homeobox protein level in Chronic kidney disease with hypertension and no diabetes (8034_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dorsal root ganglia homeobox protein in blood serum http://purl.obolibrary.org/obo/OBA_2041364 GCST90238777 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C1orf198 level in Chronic kidney disease with hypertension and no diabetes (8035_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein C1orf198 in blood serum http://purl.obolibrary.org/obo/OBA_2044873 GCST90238778 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Follitropin subunit beta level in Chronic kidney disease with hypertension and no diabetes (8036_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of follitropin subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2041621 GCST90238779 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 14 level in Chronic kidney disease with hypertension and no diabetes (8037_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238780 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating level in Chronic kidney disease with hypertension and no diabetes (8038_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating in blood serum http://purl.obolibrary.org/obo/OBA_2042644 GCST90238781 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM177A1 level in Chronic kidney disease with hypertension and no diabetes (8039_41) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein FAM177A1 in blood serum http://purl.obolibrary.org/obo/OBA_2044464 GCST90238782 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LEM domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (8040_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LEM domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044721 GCST90238783 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 9 level in Chronic kidney disease with hypertension and no diabetes (8042_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine protease inhibitor Kazal-type 9 in blood serum http://purl.obolibrary.org/obo/OBA_2043637 GCST90238784 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cartilage oligomeric matrix protein level in Chronic kidney disease with hypertension and no diabetes (8043_153) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cartilage oligomeric matrix protein in blood serum http://purl.obolibrary.org/obo/OBA_2040191 GCST90238785 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycoprotein Xg level in Chronic kidney disease with hypertension and no diabetes (8044_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycoprotein Xg in blood serum http://purl.obolibrary.org/obo/OBA_2044150 GCST90238786 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 3DL3 level in Chronic kidney disease with hypertension and no diabetes (8045_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238787 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galectin-1 level in Chronic kidney disease with hypertension and no diabetes (8046_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 galectin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020932 GCST90238788 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ferritin, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8048_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ferritin, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041627 GCST90238789 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiogenic factor with G patch and FHA domains 1 level in Chronic kidney disease with hypertension and no diabetes (8051_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of angiogenic factor with G patch and FHA domains 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040536 GCST90238790 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 4,080,687 European ancestry individuals 49,160 European ancestry individuals Affymetrix, Illumina [1385132] (imputed) 230 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245843 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 455,180 Hispanic or Latin American individuals NA Affymetrix, Illumina [1385132] (imputed) 1511 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245844 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 472,730 East Asian ancestry individuals NA Affymetrix, Illumina [1385132] (imputed) 918 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245845 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 293,593 African ancestry individuals NA Affymetrix, Illumina [1385132] (imputed) 453 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245846 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 77,890 South Asian ancestry individuals NA Illumina [1385132] (imputed) 69 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245847 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 5,314,291 European ancestry, Hispanic or Latin American, East Asian ancestry, African ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [1385132] (imputed) 12111 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245848 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 168,193 African ancestry individuals NA Affymetrix, Illumina [1373665] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245989 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 2,200,007 European ancestry, Hispanic or Latin American, East Asian ancestry, African ancestry, South Asian ancestry individuals NA Affymetrix, Illumina [1377305] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245990 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 363,856 East Asian ancestry individuals NA Affymetrix, Illumina [1355897] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245991 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 1,597,374 European ancestry individuals NA Affymetrix, Illumina [1373020] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245992 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 58,709 Hispanic or Latin American individuals NA Affymetrix, Illumina [1372262] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245993 Genome-wide genotyping array 2023-02-09 36224396 Yengo L 2022-10-12 Nature www.ncbi.nlm.nih.gov/pubmed/36224396 A saturated map of common genetic variants associated with human height. Height 60,939 South Asian ancestry individuals NA Illumina [1339059] (imputed) 0 body height http://www.ebi.ac.uk/efo/EFO_0004339 GCST90245994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Electroneutral sodium bicarbonate exchanger 1 level in Chronic kidney disease with hypertension and no diabetes (12798_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of electroneutral sodium bicarbonate exchanger 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043537 GCST90233697 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 27 level in Chronic kidney disease with hypertension and no diabetes (12799_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 27 in blood serum http://purl.obolibrary.org/obo/OBA_2044664 GCST90233698 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tubulin polymerization-promoting protein family member 2 level in Chronic kidney disease with hypertension and no diabetes (12800_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tubulin polymerization-promoting protein family member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044479 GCST90233699 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MOB kinase activator 1B level in Chronic kidney disease with hypertension and no diabetes (19177_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MOB kinase activator 1B in blood serum http://purl.obolibrary.org/obo/OBA_2042394 GCST90235137 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S ribosomal protein L12 level in Chronic kidney disease with hypertension and no diabetes (19183_164) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S ribosomal protein L12 in blood serum http://purl.obolibrary.org/obo/OBA_2043319 GCST90235138 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. STAM-binding protein level in Chronic kidney disease with hypertension and no diabetes (19187_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of STAM-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2043688 GCST90235139 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. nucleosome assembly protein 1-like 4 level in Chronic kidney disease with hypertension and no diabetes (19188_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleosome assembly protein 1-like 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042508 GCST90235140 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 14 level in Chronic kidney disease with hypertension and no diabetes (19189_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 14 in blood serum http://purl.obolibrary.org/obo/OBA_2044056 GCST90235141 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prefoldin subunit 3 level in Chronic kidney disease with hypertension and no diabetes (19193_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prefoldin subunit 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044087 GCST90235142 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. D-tyrosyl-tRNA(Tyr) deacylase 1 level in Chronic kidney disease with hypertension and no diabetes (19194_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of D-aminoacyl-tRNA deacylase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041372 GCST90235143 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S5 level in Chronic kidney disease with hypertension and no diabetes (19195_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 40S ribosomal protein S5 in blood serum http://purl.obolibrary.org/obo/OBA_2043337 GCST90235144 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeodomain-only protein level in Chronic kidney disease with hypertension and no diabetes (19196_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeodomain-only protein in blood serum http://purl.obolibrary.org/obo/OBA_2041915 GCST90235145 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerase II subunit RPB11-a level in Chronic kidney disease with hypertension and no diabetes (19199_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerase II subunit RPB11-a in blood serum http://purl.obolibrary.org/obo/OBA_2044487 GCST90235146 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5 level in Chronic kidney disease with hypertension and no diabetes (19200_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042541 GCST90235147 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase BTK level in Chronic kidney disease with hypertension and no diabetes (19202_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 tyrosine-protein kinase BTK measurement http://www.ebi.ac.uk/efo/EFO_0020819 GCST90235148 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 7,8-dihydro-8-oxoguanine triphosphatase level in Chronic kidney disease with hypertension and no diabetes (19206_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxidized purine nucleoside triphosphate hydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2042662 GCST90235149 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenosine kinase level in Chronic kidney disease with hypertension and no diabetes (19207_119) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adenosine kinase in blood serum http://purl.obolibrary.org/obo/OBA_2040521 GCST90235150 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activin receptor type-2A level in Chronic kidney disease with hypertension and no diabetes (19208_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activin receptor type-2A in blood serum http://purl.obolibrary.org/obo/OBA_2040189 GCST90235151 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NF-kappa-B inhibitor alpha level in Chronic kidney disease with hypertension and no diabetes (19209_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NF-kappa-B inhibitor alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040432 GCST90235152 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deleted in malignant brain tumors 1 protein level in Chronic kidney disease with hypertension and no diabetes (19212_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deleted in malignant brain tumors 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041320 GCST90235153 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 4 level in Chronic kidney disease with hypertension and no diabetes (19213_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine protease inhibitor Kazal-type 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043631 GCST90235154 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear transport factor 2 level in Chronic kidney disease with hypertension and no diabetes (19219_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear transport factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042679 GCST90235155 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-5B level in Chronic kidney disease with hypertension and no diabetes (19222_124) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-5B in blood serum http://purl.obolibrary.org/obo/OBA_2043167 GCST90235156 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-1A level in Chronic kidney disease with hypertension and no diabetes (19223_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-1A in blood serum http://purl.obolibrary.org/obo/OBA_2043142 GCST90235157 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 1A, Y-chromosomal level in Chronic kidney disease with hypertension and no diabetes (19224_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 1A, Y-chromosomal in blood serum http://purl.obolibrary.org/obo/OBA_2044605 GCST90235158 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 21 level in Chronic kidney disease with hypertension and no diabetes (5404_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 21 measurement http://www.ebi.ac.uk/efo/EFO_0020810 GCST90237929 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-15 level in Chronic kidney disease with hypertension and no diabetes (5410_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-15 measurement http://www.ebi.ac.uk/efo/EFO_0020211 GCST90237930 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD27 antigen level in Chronic kidney disease with hypertension and no diabetes (5412_53) 466 African American individuals NA Illumina [14870897] (imputed) 1 CD27 antigen measurement http://www.ebi.ac.uk/efo/EFO_0008078 GCST90237931 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 11A level in Chronic kidney disease with hypertension and no diabetes (5424_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 11A measurement http://www.ebi.ac.uk/efo/EFO_0020800 GCST90237932 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type substrate 1 level in Chronic kidney disease with hypertension and no diabetes (5430_66) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tyrosine-protein phosphatase non-receptor type substrate 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040362 GCST90237933 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein, heart level in Chronic kidney disease with hypertension and no diabetes (5437_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 fatty acid-binding protein, heart measurement http://www.ebi.ac.uk/efo/EFO_0020373 GCST90237934 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Troponin I, fast skeletal muscle level in Chronic kidney disease with hypertension and no diabetes (5440_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 troponin i, fast skeletal muscle measurement http://www.ebi.ac.uk/efo/EFO_0020789 GCST90237935 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin enhancer-binding factor 2 level in Chronic kidney disease with hypertension and no diabetes (12665_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin enhancer-binding factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042017 GCST90233604 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine deaminase level in Chronic kidney disease with hypertension and no diabetes (12667_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine deaminase in blood serum http://purl.obolibrary.org/obo/OBA_2041695 GCST90233605 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein sorting-associated protein 4B level in Chronic kidney disease with hypertension and no diabetes (12668_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vacuolar protein sorting-associated protein 4B in blood serum http://purl.obolibrary.org/obo/OBA_2044112 GCST90233606 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase HECW1 level in Chronic kidney disease with hypertension and no diabetes (12669_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase HECW1 in blood serum http://purl.obolibrary.org/obo/OBA_2041854 GCST90233607 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell cycle checkpoint protein RAD1 level in Chronic kidney disease with hypertension and no diabetes (12670_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell cycle checkpoint protein RAD1 in blood serum http://purl.obolibrary.org/obo/OBA_2043178 GCST90233608 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sulfotransferase family cytosolic 1B member 1 level in Chronic kidney disease with hypertension and no diabetes (12671_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 1B1 in blood serum http://purl.obolibrary.org/obo/OBA_2043726 GCST90233609 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartate--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (12675_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aspartate--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2041231 GCST90233610 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C and casein kinase substrate in neurons protein 1 level in Chronic kidney disease with hypertension and no diabetes (12676_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein kinase C and casein kinase substrate in neurons protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042739 GCST90233611 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein flightless-1 homolog level in Chronic kidney disease with hypertension and no diabetes (12677_164) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein flightless-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041594 GCST90233612 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. U1 small nuclear ribonucleoprotein A level in Chronic kidney disease with hypertension and no diabetes (12678_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of U1 small nuclear ribonucleoprotein A in blood serum http://purl.obolibrary.org/obo/OBA_2043572 GCST90233613 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 21 level in Chronic kidney disease with hypertension and no diabetes (12681_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 21 in blood serum http://purl.obolibrary.org/obo/OBA_2044060 GCST90233614 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kynurenine--oxoglutarate transaminase 3 level in Chronic kidney disease with hypertension and no diabetes (12682_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kynurenine--oxoglutarate transaminase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040925 GCST90233615 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydropyrimidinase-related protein 5 level in Chronic kidney disease with hypertension and no diabetes (12683_156) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydropyrimidinase-related protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041360 GCST90233616 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adseverin level in Chronic kidney disease with hypertension and no diabetes (12684_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of scinderin in blood serum http://purl.obolibrary.org/obo/OBA_2043401 GCST90233617 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homer protein homolog 2 level in Chronic kidney disease with hypertension and no diabetes (12685_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homer protein homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041913 GCST90233618 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-mercaptopyruvate sulfurtransferase level in Chronic kidney disease with hypertension and no diabetes (12686_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 3-mercaptopyruvate sulfurtransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042408 GCST90233619 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2,4-dienoyl-CoA reductase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12687_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing], mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041262 GCST90233620 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosomal protein S6 kinase alpha-6 level in Chronic kidney disease with hypertension and no diabetes (12688_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosomal protein S6 kinase alpha-6 in blood serum http://purl.obolibrary.org/obo/OBA_2043339 GCST90233621 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 2 subunit 1 level in Chronic kidney disease with hypertension and no diabetes (19259_176) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 2 subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041444 GCST90235184 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ domain-containing protein GIPC1 level in Chronic kidney disease with hypertension and no diabetes (19260_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ domain-containing protein GIPC1 in blood serum http://purl.obolibrary.org/obo/OBA_2041721 GCST90235185 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntenin-2 level in Chronic kidney disease with hypertension and no diabetes (19261_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntenin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043412 GCST90235186 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Very long-chain specific acyl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19262_219) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of very long-chain specific acyl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040472 GCST90235187 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 4E level in Chronic kidney disease with hypertension and no diabetes (19263_147) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 4E in blood serum http://purl.obolibrary.org/obo/OBA_2041452 GCST90235188 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Replication protein A 32 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (19264_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of replication protein A 32 kDa subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043314 GCST90235189 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-complex protein 1 subunit alpha level in Chronic kidney disease with hypertension and no diabetes (19265_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of T-complex protein 1 subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040939 GCST90235190 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras GTPase-activating protein-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (19266_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras GTPase-activating protein-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041644 GCST90235191 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hydroxyacylglutathione hydrolase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19267_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hydroxyacylglutathione hydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2041834 GCST90235192 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein G(i) subunit alpha-1 level in Chronic kidney disease with hypertension and no diabetes (19271_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide-binding protein G(i) subunit alpha-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041747 GCST90235193 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peflin level in Chronic kidney disease with hypertension and no diabetes (19272_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of peflin in blood serum http://purl.obolibrary.org/obo/OBA_2042843 GCST90235194 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione reductase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19273_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutathione reductase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041800 GCST90235195 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-1-syntrophin level in Chronic kidney disease with hypertension and no diabetes (19274_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-1-syntrophin in blood serum http://purl.obolibrary.org/obo/OBA_2043579 GCST90235196 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19275_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isocitrate dehydrogenase [NAD] subunit gamma, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041970 GCST90235197 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small nuclear ribonucleoprotein G level in Chronic kidney disease with hypertension and no diabetes (19276_124) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small nuclear ribonucleoprotein G in blood serum http://purl.obolibrary.org/obo/OBA_2043578 GCST90235198 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (19277_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thiosulfate:glutathione sulfurtransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044712 GCST90235199 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-1B level in Chronic kidney disease with hypertension and no diabetes (19278_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-1B in blood serum http://purl.obolibrary.org/obo/OBA_2043143 GCST90235200 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (19279_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinol-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043211 GCST90235201 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor MafG level in Chronic kidney disease with hypertension and no diabetes (19281_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor MafG in blood serum http://purl.obolibrary.org/obo/OBA_2042262 GCST90235202 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-13 level in Chronic kidney disease with hypertension and no diabetes (19282_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-13 in blood serum http://purl.obolibrary.org/obo/OBA_2043139 GCST90235203 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin light chain 5 level in Chronic kidney disease with hypertension and no diabetes (19286_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin light chain 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042480 GCST90235204 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Density-regulated protein level in Chronic kidney disease with hypertension and no diabetes (19287_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of density-regulated protein in blood serum http://purl.obolibrary.org/obo/OBA_2041286 GCST90235205 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uroporphyrinogen decarboxylase level in Chronic kidney disease with hypertension and no diabetes (19289_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uroporphyrinogen decarboxylase in blood serum http://purl.obolibrary.org/obo/OBA_2044046 GCST90235206 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hypoxanthine-guanine phosphoribosyltransferase level in Chronic kidney disease with hypertension and no diabetes (19290_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hypoxanthine-guanine phosphoribosyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041923 GCST90235207 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calsequestrin-2 level in Chronic kidney disease with hypertension and no diabetes (19291_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calsequestrin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040906 GCST90235208 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Septin-10 level in Chronic kidney disease with hypertension and no diabetes (12690_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of septin-10 in blood serum http://purl.obolibrary.org/obo/OBA_2043447 GCST90233622 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine hydroxymethyltransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12691_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine hydroxymethyltransferase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043504 GCST90233623 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase, H3 lysine-79 specific level in Chronic kidney disease with hypertension and no diabetes (12692_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone-lysine N-methyltransferase, H3 lysine-79 specific in blood serum http://purl.obolibrary.org/obo/OBA_2041346 GCST90233624 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 domain-binding glutamic acid-rich-like protein level in Chronic kidney disease with hypertension and no diabetes (12693_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adapter SH3BGRL in blood serum http://purl.obolibrary.org/obo/OBA_2044419 GCST90233625 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable dimethyladenosine transferase level in Chronic kidney disease with hypertension and no diabetes (12694_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable dimethyladenosine transferase in blood serum http://purl.obolibrary.org/obo/OBA_2044519 GCST90233626 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 12 level in Chronic kidney disease with hypertension and no diabetes (12695_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 12 in blood serum http://purl.obolibrary.org/obo/OBA_2042120 GCST90233627 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein arginine N-methyltransferase 3 level in Chronic kidney disease with hypertension and no diabetes (12696_166) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein arginine N-methyltransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043033 GCST90233628 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol 5-phosphate 4-kinase type-2 alpha level in Chronic kidney disease with hypertension and no diabetes (12697_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol 5-phosphate 4-kinase type-2 alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042897 GCST90233629 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Importin subunit alpha-3 level in Chronic kidney disease with hypertension and no diabetes (12698_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of importin subunit alpha-3 in blood serum http://purl.obolibrary.org/obo/OBA_2042133 GCST90233630 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-citrate synthase level in Chronic kidney disease with hypertension and no diabetes (12700_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-citrate synthase in blood serum http://purl.obolibrary.org/obo/OBA_2040478 GCST90233631 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase pellino homolog 2 level in Chronic kidney disease with hypertension and no diabetes (12702_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase pellino homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042844 GCST90233632 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase Nek7 level in Chronic kidney disease with hypertension and no diabetes (12703_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase Nek7 in blood serum http://purl.obolibrary.org/obo/OBA_2042556 GCST90233633 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH2 domain-containing protein 3C level in Chronic kidney disease with hypertension and no diabetes (12704_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH2 domain-containing protein 3C in blood serum http://purl.obolibrary.org/obo/OBA_2043490 GCST90233634 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable E3 ubiquitin-protein ligase HERC1 level in Chronic kidney disease with hypertension and no diabetes (12705_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable E3 ubiquitin-protein ligase HERC1 in blood serum http://purl.obolibrary.org/obo/OBA_2044311 GCST90233635 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase MRCK alpha level in Chronic kidney disease with hypertension and no diabetes (12706_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase MRCK alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040954 GCST90233636 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydropyrimidinase-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (12707_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydropyrimidinase-related protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041358 GCST90233637 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lethal(3)malignant brain tumor-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (12708_91) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lethal(3)malignant brain tumor-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042153 GCST90233638 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone H1x level in Chronic kidney disease with hypertension and no diabetes (12709_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone H1.10 in blood serum http://purl.obolibrary.org/obo/OBA_2041827 GCST90233639 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gap junction alpha-8 protein level in Chronic kidney disease with hypertension and no diabetes (12711_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gap junction alpha-8 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041722 GCST90233640 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High mobility group protein 20A level in Chronic kidney disease with hypertension and no diabetes (12712_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high mobility group protein 20A in blood serum http://purl.obolibrary.org/obo/OBA_2041885 GCST90233641 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 19 level in Chronic kidney disease with hypertension and no diabetes (12713_365) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 19 in blood serum http://purl.obolibrary.org/obo/OBA_2043258 GCST90233642 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-1 complex subunit gamma-like 2 level in Chronic kidney disease with hypertension and no diabetes (12714_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-1 complex subunit gamma-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040609 GCST90233643 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 175 level in Chronic kidney disease with hypertension and no diabetes (12716_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 175 in blood serum http://purl.obolibrary.org/obo/OBA_2044191 GCST90233644 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TOX high mobility group box family member 3 level in Chronic kidney disease with hypertension and no diabetes (12717_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TOX high mobility group box family member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044553 GCST90233645 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase NIMA-interacting 4 level in Chronic kidney disease with hypertension and no diabetes (12718_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase NIMA-interacting 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042895 GCST90233646 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell linker protein level in Chronic kidney disease with hypertension and no diabetes (19225_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell linker protein in blood serum http://purl.obolibrary.org/obo/OBA_2040804 GCST90235159 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Basic leucine zipper transcriptional factor ATF-like level in Chronic kidney disease with hypertension and no diabetes (19227_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of basic leucine zipper transcriptional factor ATF-like in blood serum http://purl.obolibrary.org/obo/OBA_2040781 GCST90235160 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BAG family molecular chaperone regulator 2 level in Chronic kidney disease with hypertension and no diabetes (19228_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BAG family molecular chaperone regulator 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040766 GCST90235161 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homer protein homolog 1 level in Chronic kidney disease with hypertension and no diabetes (19229_92) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of homer protein homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041912 GCST90235162 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase theta-1 level in Chronic kidney disease with hypertension and no diabetes (19230_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutathione S-transferase theta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041809 GCST90235163 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein tyrosine phosphatase type IVA 3 level in Chronic kidney disease with hypertension and no diabetes (19231_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein tyrosine phosphatase type IVA 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043099 GCST90235164 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Copper transport protein ATOX1 level in Chronic kidney disease with hypertension and no diabetes (19233_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of copper transport protein ATOX1 in blood serum http://purl.obolibrary.org/obo/OBA_2040725 GCST90235165 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activated RNA polymerase II transcriptional coactivator p15 level in Chronic kidney disease with hypertension and no diabetes (19236_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activated RNA polymerase II transcriptional coactivator p15 in blood serum http://purl.obolibrary.org/obo/OBA_2043722 GCST90235166 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. D-dopachrome decarboxylase level in Chronic kidney disease with hypertension and no diabetes (19237_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of D-dopachrome decarboxylase in blood serum http://purl.obolibrary.org/obo/OBA_2041257 GCST90235167 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamine synthetase level in Chronic kidney disease with hypertension and no diabetes (19238_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamine synthetase in blood serum http://purl.obolibrary.org/obo/OBA_2041739 GCST90235168 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor 1 level in Chronic kidney disease with hypertension and no diabetes (19239_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040639 GCST90235169 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 28 kDa heat- and acid-stable phosphoprotein level in Chronic kidney disease with hypertension and no diabetes (19240_265) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 28 kDa heat- and acid-stable phosphoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2042811 GCST90235170 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol-binding protein 5 level in Chronic kidney disease with hypertension and no diabetes (19241_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinol-binding protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043213 GCST90235171 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prefoldin subunit 1 level in Chronic kidney disease with hypertension and no diabetes (19242_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prefoldin subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042848 GCST90235172 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prefoldin subunit 2 level in Chronic kidney disease with hypertension and no diabetes (19243_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prefoldin subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042849 GCST90235173 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 D1 level in Chronic kidney disease with hypertension and no diabetes (19247_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 D1 in blood serum http://purl.obolibrary.org/obo/OBA_2040420 GCST90235174 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysine--tRNA ligase level in Chronic kidney disease with hypertension and no diabetes (19249_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic-type lysine--tRNA ligase in blood serum http://purl.obolibrary.org/obo/OBA_2042082 GCST90235175 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-Myc-binding protein level in Chronic kidney disease with hypertension and no diabetes (19250_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of c-Myc-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2042477 GCST90235176 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serglycin level in Chronic kidney disease with hypertension and no diabetes (19251_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serglycin in blood serum http://purl.obolibrary.org/obo/OBA_2043653 GCST90235177 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-2 level in Chronic kidney disease with hypertension and no diabetes (19252_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit beta type-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040404 GCST90235178 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-2B level in Chronic kidney disease with hypertension and no diabetes (19253_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-2B in blood serum http://purl.obolibrary.org/obo/OBA_2043152 GCST90235179 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GMP reductase 1 level in Chronic kidney disease with hypertension and no diabetes (19254_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GMP reductase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041745 GCST90235180 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NTF2-related export protein 2 level in Chronic kidney disease with hypertension and no diabetes (19255_124) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of NTF2-related export protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042684 GCST90235181 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Clathrin light chain A level in Chronic kidney disease with hypertension and no diabetes (19257_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of clathrin light chain A in blood serum http://purl.obolibrary.org/obo/OBA_2041059 GCST90235182 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaryl-CoA dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19258_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutaryl-CoA dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041685 GCST90235183 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin enhancer-binding factor 3 level in Chronic kidney disease with hypertension and no diabetes (12759_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin enhancer-binding factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042018 GCST90233672 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 774 level in Chronic kidney disease with hypertension and no diabetes (12760_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 774 in blood serum http://purl.obolibrary.org/obo/OBA_2044215 GCST90233673 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 precursor protein-binding family B member 2 level in Chronic kidney disease with hypertension and no diabetes (12761_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233674 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 334 level in Chronic kidney disease with hypertension and no diabetes (12763_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 334 in blood serum http://purl.obolibrary.org/obo/OBA_2044201 GCST90233675 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Engulfment and cell motility protein 1 level in Chronic kidney disease with hypertension and no diabetes (12764_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of engulfment and cell motility protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041472 GCST90233676 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable G-protein coupled receptor 142 level in Chronic kidney disease with hypertension and no diabetes (12766_33) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of probable G-protein coupled receptor 142 in blood serum http://purl.obolibrary.org/obo/OBA_2040308 GCST90233677 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1 regulatory subunit 3B level in Chronic kidney disease with hypertension and no diabetes (12768_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1 regulatory subunit 3B in blood serum http://purl.obolibrary.org/obo/OBA_2043004 GCST90233678 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 180 level in Chronic kidney disease with hypertension and no diabetes (12771_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 180 in blood serum http://purl.obolibrary.org/obo/OBA_2044193 GCST90233679 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear pore complex protein Nup98-Nup96 level in Chronic kidney disease with hypertension and no diabetes (12772_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear pore complex protein Nup98-Nup96 in blood serum http://purl.obolibrary.org/obo/OBA_2042678 GCST90233680 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 level in Chronic kidney disease with hypertension and no diabetes (12774_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040220 GCST90233681 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High mobility group protein B3 level in Chronic kidney disease with hypertension and no diabetes (12775_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high mobility group protein B3 in blood serum http://purl.obolibrary.org/obo/OBA_2041890 GCST90233682 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Splicing factor 1 level in Chronic kidney disease with hypertension and no diabetes (12777_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of splicing factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043472 GCST90233683 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PR domain zinc finger protein 4 level in Chronic kidney disease with hypertension and no diabetes (12779_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PR domain zinc finger protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043019 GCST90233684 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RISC-loading complex subunit TARBP2 level in Chronic kidney disease with hypertension and no diabetes (12781_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RISC-loading complex subunit TARBP2 in blood serum http://purl.obolibrary.org/obo/OBA_2043777 GCST90233685 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein M level in Chronic kidney disease with hypertension and no diabetes (12783_29) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of heterogeneous nuclear ribonucleoprotein M in blood serum http://purl.obolibrary.org/obo/OBA_2041908 GCST90233686 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 precursor protein-binding family B member 3 level in Chronic kidney disease with hypertension and no diabetes (12784_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233687 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional regulator Kaiso level in Chronic kidney disease with hypertension and no diabetes (12785_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional regulator Kaiso in blood serum http://purl.obolibrary.org/obo/OBA_2044173 GCST90233688 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycerophosphocholine phosphodiesterase GPCPD1 level in Chronic kidney disease with hypertension and no diabetes (12786_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycerophosphocholine phosphodiesterase GPCPD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044618 GCST90233689 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 134 level in Chronic kidney disease with hypertension and no diabetes (12787_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 134 in blood serum http://purl.obolibrary.org/obo/OBA_2044188 GCST90233690 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SAGA-associated factor 29 homolog level in Chronic kidney disease with hypertension and no diabetes (12788_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SAGA-associated factor 29 in blood serum http://purl.obolibrary.org/obo/OBA_2040926 GCST90233691 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 51 level in Chronic kidney disease with hypertension and no diabetes (12790_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial potassium channel in blood serum http://purl.obolibrary.org/obo/OBA_2044708 GCST90233692 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Piwi-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (12793_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of piwi-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042905 GCST90233693 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NACHT, LRR and PYD domains-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (12794_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NACHT, LRR and PYD domains-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042593 GCST90233694 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 566 level in Chronic kidney disease with hypertension and no diabetes (12795_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 566 in blood serum http://purl.obolibrary.org/obo/OBA_2044209 GCST90233695 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diphosphoinositol polyphosphate phosphohydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (12796_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diphosphoinositol polyphosphate phosphohydrolase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042671 GCST90233696 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquilin-4 level in Chronic kidney disease with hypertension and no diabetes (12720_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquilin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2044014 GCST90233647 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tax1-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (12721_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Tax1-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043781 GCST90233648 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cold-inducible RNA-binding protein level in Chronic kidney disease with hypertension and no diabetes (12724_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cold-inducible RNA-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2041033 GCST90233649 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulatory factor X-associated protein level in Chronic kidney disease with hypertension and no diabetes (12726_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulatory factor X-associated protein in blood serum http://purl.obolibrary.org/obo/OBA_2043250 GCST90233650 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin F2 receptor negative regulator level in Chronic kidney disease with hypertension and no diabetes (12727_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of prostaglandin F2 receptor negative regulator in blood serum http://purl.obolibrary.org/obo/OBA_2040356 GCST90233651 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome assembly chaperone 3 level in Chronic kidney disease with hypertension and no diabetes (12729_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome assembly chaperone 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043081 GCST90233652 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinetochore protein NDC80 homolog level in Chronic kidney disease with hypertension and no diabetes (12730_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kinetochore protein NDC80 in blood serum http://purl.obolibrary.org/obo/OBA_2042532 GCST90233653 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family A member 7 level in Chronic kidney disease with hypertension and no diabetes (12731_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family A member 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044342 GCST90233654 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAGUK p55 subfamily member 7 level in Chronic kidney disease with hypertension and no diabetes (12732_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MAGUK p55 subfamily member 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042407 GCST90233655 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin-like protein KIF22 level in Chronic kidney disease with hypertension and no diabetes (12734_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kinesin-like protein KIF22 in blood serum http://purl.obolibrary.org/obo/OBA_2042098 GCST90233656 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cold shock domain-containing protein E1 level in Chronic kidney disease with hypertension and no diabetes (12735_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cold shock domain-containing protein E1 in blood serum http://purl.obolibrary.org/obo/OBA_2041166 GCST90233657 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plastin-1 level in Chronic kidney disease with hypertension and no diabetes (12737_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plastin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042931 GCST90233658 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nischarin level in Chronic kidney disease with hypertension and no diabetes (12738_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nischarin in blood serum http://purl.obolibrary.org/obo/OBA_2042583 GCST90233659 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FEV level in Chronic kidney disease with hypertension and no diabetes (12740_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FEV in blood serum http://purl.obolibrary.org/obo/OBA_2041572 GCST90233660 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 8B level in Chronic kidney disease with hypertension and no diabetes (12742_160) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 8B in blood serum http://purl.obolibrary.org/obo/OBA_2044455 GCST90233661 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BAG family molecular chaperone regulator 5 level in Chronic kidney disease with hypertension and no diabetes (12743_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BAG family molecular chaperone regulator 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040769 GCST90233662 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytohesin-4 level in Chronic kidney disease with hypertension and no diabetes (12746_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytohesin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041220 GCST90233663 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (12747_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044352 GCST90233664 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bromodomain testis-specific protein level in Chronic kidney disease with hypertension and no diabetes (12748_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bromodomain testis-specific protein in blood serum http://purl.obolibrary.org/obo/OBA_2040826 GCST90233665 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin beta-2 level in Chronic kidney disease with hypertension and no diabetes (12750_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integrin beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040372 GCST90233666 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc fingers and homeoboxes protein 1 level in Chronic kidney disease with hypertension and no diabetes (12751_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc fingers and homeoboxes protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044184 GCST90233667 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 precursor protein-binding family B member 2 level in Chronic kidney disease with hypertension and no diabetes (12753_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233668 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cold shock domain-containing protein C2 level in Chronic kidney disease with hypertension and no diabetes (12754_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cold shock domain-containing protein C2 in blood serum http://purl.obolibrary.org/obo/OBA_2041165 GCST90233669 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription regulator protein BACH2 level in Chronic kidney disease with hypertension and no diabetes (12756_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription regulator protein BACH2 in blood serum http://purl.obolibrary.org/obo/OBA_2040764 GCST90233670 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate receptor ionotropic, delta-2 level in Chronic kidney disease with hypertension and no diabetes (12758_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutamate receptor ionotropic, delta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041790 GCST90233671 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin-like protein KIF23 level in Chronic kidney disease with hypertension and no diabetes (5228_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 kinesin-like protein KIF23 measurement http://www.ebi.ac.uk/efo/EFO_0020522 GCST90237879 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inosine-5'-monophosphate dehydrogenase 1 level in Chronic kidney disease with hypertension and no diabetes (5229_90) 466 African American individuals NA Illumina [14870897] (imputed) 0 inosine-5'-monophosphate dehydrogenase 1 measurement http://www.ebi.ac.uk/efo/EFO_0008158 GCST90237880 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-hydroxy-3-methylglutaryl-coenzyme A reductase level in Chronic kidney disease with hypertension and no diabetes (5230_99) 466 African American individuals NA Illumina [14870897] (imputed) 0 3-hydroxy-3-methylglutaryl-coenzymeAreductase measurement http://www.ebi.ac.uk/efo/EFO_0020113 GCST90237881 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proprotein convertase subtilisin/kexin type 9 level in Chronic kidney disease with hypertension and no diabetes (5231_79) 466 African American individuals NA Illumina [14870897] (imputed) 1 proprotein convertase subtilisin/kexin type 9 measurement http://www.ebi.ac.uk/efo/EFO_0009312 GCST90237882 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor subfamily 1 group D member 1 level in Chronic kidney disease with hypertension and no diabetes (5236_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 nuclear receptor subfamily 1 group d member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020614 GCST90237883 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase E level in Chronic kidney disease with hypertension and no diabetes (5238_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptidyl-prolyl cis-trans isomerase E measurement http://www.ebi.ac.uk/efo/EFO_0008257 GCST90237884 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity mitogen-activated protein kinase kinase 4 level in Chronic kidney disease with hypertension and no diabetes (5242_37) 466 African American individuals NA Illumina [14870897] (imputed) 1 dual specificity mitogen-activated protein kinase kinase 4 measurement http://www.ebi.ac.uk/efo/EFO_0008113 GCST90237885 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AMP Kinase (alpha2beta2gamma1) level in Chronic kidney disease with hypertension and no diabetes (5245_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 amp kinase (alpha2beta2gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020143 GCST90237886 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase F, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (5248_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 peptidyl-prolyl cis-trans isomerase F, mitochondrial measurement http://www.ebi.ac.uk/efo/EFO_0020627 GCST90237887 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase 17B level in Chronic kidney disease with hypertension and no diabetes (5249_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase 17B measurement http://www.ebi.ac.uk/efo/EFO_0008281 GCST90237888 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A level in Chronic kidney disease with hypertension and no diabetes (5252_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 dual 3',5'-cyclic-amp and -gmp phosphodiesterase 11a measurement http://www.ebi.ac.uk/efo/EFO_0020334 GCST90237889 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cGMP-inhibited 3',5'-cyclic phosphodiesterase A level in Chronic kidney disease with hypertension and no diabetes (5254_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 cGMP-inhibited 3',5'-cyclic phosphodiesterase A measurement http://www.ebi.ac.uk/efo/EFO_0020255 GCST90237890 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-specific 3',5'-cyclic phosphodiesterase 4D level in Chronic kidney disease with hypertension and no diabetes (5255_22) 466 African American individuals NA Illumina [14870897] (imputed) 1 cAMP-specific 3',5'-cyclic phosphodiesterase 4D measurement http://www.ebi.ac.uk/efo/EFO_0020224 GCST90237891 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cGMP-specific 3',5'-cyclic phosphodiesterase level in Chronic kidney disease with hypertension and no diabetes (5256_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 cGMP-specific 3',5'-cyclic phosphodiesterase measurement http://www.ebi.ac.uk/efo/EFO_0008081 GCST90237892 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Non-receptor tyrosine-protein kinase TYK2 level in Chronic kidney disease with hypertension and no diabetes (5260_80) 466 African American individuals NA Illumina [14870897] (imputed) 1 non-receptor tyrosine-protein kinase TYK2 measurement http://www.ebi.ac.uk/efo/EFO_0008251 GCST90237893 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Abelson tyrosine-protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (5261_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 Abelson tyrosine-protein kinase 2 measurement http://www.ebi.ac.uk/efo/EFO_0008012 GCST90237894 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Breast cancer anti-estrogen resistance protein 3 level in Chronic kidney disease with hypertension and no diabetes (5262_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 breast cancer anti-estrogen resistance protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008040 GCST90237895 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calreticulin level in Chronic kidney disease with hypertension and no diabetes (5264_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 calreticulin measurement http://www.ebi.ac.uk/efo/EFO_0020221 GCST90237896 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRB2-related adapter protein 2 level in Chronic kidney disease with hypertension and no diabetes (5265_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 grb2-related adapter protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020420 GCST90237897 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrix metalloproteinase-16 level in Chronic kidney disease with hypertension and no diabetes (5268_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 matrix metalloproteinase-16 measurement http://www.ebi.ac.uk/efo/EFO_0020559 GCST90237898 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SHC-transforming protein 1 level in Chronic kidney disease with hypertension and no diabetes (5272_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 shc-transforming protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020738 GCST90237899 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proto-oncogene vav level in Chronic kidney disease with hypertension and no diabetes (5275_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 proto-oncogene vav measurement http://www.ebi.ac.uk/efo/EFO_0021988 GCST90237900 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial glutamate carrier 2 level in Chronic kidney disease with hypertension and no diabetes (5280_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitochondrial glutamate carrier 2 measurement http://www.ebi.ac.uk/efo/EFO_0020572 GCST90237901 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eotaxin level in Chronic kidney disease with hypertension and no diabetes (5301_7) 466 African American individuals NA Illumina [14870897] (imputed) 5 eotaxin measurement http://www.ebi.ac.uk/efo/EFO_0008122 GCST90237902 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation factor IXab level in Chronic kidney disease with hypertension and no diabetes (5307_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 coagulation factor IXAB measurement http://www.ebi.ac.uk/efo/EFO_0020264 GCST90237903 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apolipoprotein E (isoform E2) level in Chronic kidney disease with hypertension and no diabetes (5312_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of apolipoprotein E in blood serum http://purl.obolibrary.org/obo/OBA_2040627 GCST90237904 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Troponin T, cardiac muscle level in Chronic kidney disease with hypertension and no diabetes (5315_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of troponin T, cardiac muscle in blood serum http://purl.obolibrary.org/obo/OBA_2043893 GCST90237905 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A9 level in Chronic kidney disease with hypertension and no diabetes (5339_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein s100-a9 measurement http://www.ebi.ac.uk/efo/EFO_0020687 GCST90237906 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Caspase-10 level in Chronic kidney disease with hypertension and no diabetes (5340_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 caspase-10 measurement http://www.ebi.ac.uk/efo/EFO_0020239 GCST90237907 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase E level in Chronic kidney disease with hypertension and no diabetes (5343_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 carboxypeptidase e measurement http://www.ebi.ac.uk/efo/EFO_0020234 GCST90237908 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Copine-1 level in Chronic kidney disease with hypertension and no diabetes (5346_24) 466 African American individuals NA Illumina [14870897] (imputed) 1 copine-1 measurement http://www.ebi.ac.uk/efo/EFO_0008102 GCST90237909 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G2/mitotic-specific cyclin-B1 level in Chronic kidney disease with hypertension and no diabetes (5347_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 g2/mitotic-specific cyclin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0020396 GCST90237910 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (5349_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 delta-like protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020316 GCST90237911 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glypican-6 level in Chronic kidney disease with hypertension and no diabetes (5350_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 glypican-6 measurement http://www.ebi.ac.uk/efo/EFO_0021871 GCST90237912 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoproteins A2/B1 level in Chronic kidney disease with hypertension and no diabetes (5351_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 heterogeneous nuclear ribonucleoproteins A2/B1 measurement http://www.ebi.ac.uk/efo/EFO_0020444 GCST90237913 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 14 level in Chronic kidney disease with hypertension and no diabetes (5352_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0020805 GCST90237914 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor antagonist protein level in Chronic kidney disease with hypertension and no diabetes (5353_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin 1 receptor antagonist measurement http://www.ebi.ac.uk/efo/EFO_0004754 GCST90237915 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type I cytoskeletal 18 level in Chronic kidney disease with hypertension and no diabetes (5354_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 keratin, type I cytoskeletal 18 measurement http://www.ebi.ac.uk/efo/EFO_0020517 GCST90237916 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor ligand superfamily member 14 level in Chronic kidney disease with hypertension and no diabetes (5355_69) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor ligand superfamily member 14 measurement http://www.ebi.ac.uk/efo/EFO_0010613 GCST90237917 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrophage migration inhibitory factor level in Chronic kidney disease with hypertension and no diabetes (5356_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 macrophage migration inhibitory factor measurement http://www.ebi.ac.uk/efo/EFO_0008221 GCST90237918 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-4, X-linked level in Chronic kidney disease with hypertension and no diabetes (5357_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuroligin-4, x-linked measurement http://www.ebi.ac.uk/efo/EFO_0020601 GCST90237919 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteomodulin level in Chronic kidney disease with hypertension and no diabetes (5358_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 osteomodulin measurement http://www.ebi.ac.uk/efo/EFO_0020619 GCST90237920 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase pim-1 level in Chronic kidney disease with hypertension and no diabetes (5359_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase PIM-1 measurement http://www.ebi.ac.uk/efo/EFO_0020731 GCST90237921 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RAC-beta serine/threonine-protein kinase level in Chronic kidney disease with hypertension and no diabetes (5360_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 RAC-beta serine/threonine-protein kinase measurement http://www.ebi.ac.uk/efo/EFO_0021989 GCST90237922 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-3E level in Chronic kidney disease with hypertension and no diabetes (5363_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 semaphorin-3E measurement http://www.ebi.ac.uk/efo/EFO_0008279 GCST90237923 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein SET level in Chronic kidney disease with hypertension and no diabetes (5364_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein set measurement http://www.ebi.ac.uk/efo/EFO_0020688 GCST90237924 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 13C level in Chronic kidney disease with hypertension and no diabetes (5383_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 13C measurement http://www.ebi.ac.uk/efo/EFO_0020804 GCST90237925 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor IIIB 90 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (5384_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 transcription factor IIIb 90 kda subunit measurement http://www.ebi.ac.uk/efo/EFO_0020778 GCST90237926 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 6 level in Chronic kidney disease with hypertension and no diabetes (5392_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 6 measurement http://www.ebi.ac.uk/efo/EFO_0010610 GCST90237927 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leptin receptor, soluble level in Chronic kidney disease with hypertension and no diabetes (5400_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 leptin receptor measurement http://www.ebi.ac.uk/efo/EFO_0004635 GCST90237928 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase parkin level in Chronic kidney disease with hypertension and no diabetes (13013_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase parkin in blood serum http://purl.obolibrary.org/obo/OBA_2042762 GCST90233783 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor protein p53-inducible protein 11 level in Chronic kidney disease with hypertension and no diabetes (13022_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tumor protein p53-inducible protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2043904 GCST90233784 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor receptor substrate 2 level in Chronic kidney disease with hypertension and no diabetes (13025_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor receptor substrate 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041618 GCST90233785 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromobox protein homolog 7 level in Chronic kidney disease with hypertension and no diabetes (13027_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromobox protein homolog 7 in blood serum http://purl.obolibrary.org/obo/OBA_2040923 GCST90233786 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beclin-1 level in Chronic kidney disease with hypertension and no diabetes (13032_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beclin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040792 GCST90233787 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear inhibitor of protein phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (13039_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear inhibitor of protein phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043005 GCST90233788 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TNF receptor-associated factor 4 level in Chronic kidney disease with hypertension and no diabetes (13041_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TNF receptor-associated factor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040406 GCST90233789 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Potassium voltage-gated channel subfamily A member 10 level in Chronic kidney disease with hypertension and no diabetes (13042_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-gated potassium channel subunit KCNA10 in blood serum http://purl.obolibrary.org/obo/OBA_2040224 GCST90233790 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATPase family AAA domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (13043_157) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATPase family AAA domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040710 GCST90233791 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor susceptibility gene 101 protein level in Chronic kidney disease with hypertension and no diabetes (13044_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor susceptibility gene 101 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043947 GCST90233792 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium- and chloride-dependent neutral and basic amino acid transporter B(0+) level in Chronic kidney disease with hypertension and no diabetes (13053_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium- and chloride-dependent neutral and basic amino acid transporter B(0+) in blood serum http://purl.obolibrary.org/obo/OBA_2043540 GCST90233793 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Profilin-2 level in Chronic kidney disease with hypertension and no diabetes (13054_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of profilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042856 GCST90233794 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PH and SEC7 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (13055_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PH and SEC7 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043053 GCST90233795 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TOM1-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (19356_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of TOM1-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043900 GCST90235233 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vesicle-associated membrane protein 7 level in Chronic kidney disease with hypertension and no diabetes (19357_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vesicle-associated membrane protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044078 GCST90235234 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat transmembrane neuronal protein 1 level in Chronic kidney disease with hypertension and no diabetes (19360_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 leucine-rich repeat transmembrane neuronal protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020531 GCST90235235 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Matrilin-3 level in Chronic kidney disease with hypertension and no diabetes (19361_78) 466 African American individuals NA Illumina [14870897] (imputed) 1 matrilin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020556 GCST90235236 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proliferating cell nuclear antigen level in Chronic kidney disease with hypertension and no diabetes (19364_163) 466 African American individuals NA Illumina [14870897] (imputed) 0 proliferating cell nuclear antigen measurement http://www.ebi.ac.uk/efo/EFO_0020657 GCST90235237 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Branched-chain-amino-acid aminotransferase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19365_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of branched-chain-amino-acid aminotransferase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040784 GCST90235238 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Enoyl-CoA delta isomerase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19367_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of enoyl-CoA Delta isomerase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041238 GCST90235239 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone acetyltransferase KAT2A level in Chronic kidney disease with hypertension and no diabetes (19369_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone acetyltransferase KAT2A in blood serum http://purl.obolibrary.org/obo/OBA_2041690 GCST90235240 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan sulfate glucosamine 3-O-sulfotransferase 4 level in Chronic kidney disease with hypertension and no diabetes (19370_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of heparan sulfate glucosamine 3-O-sulfotransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041933 GCST90235241 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated protein RP/EB family member 1 level in Chronic kidney disease with hypertension and no diabetes (19371_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated protein RP/EB family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042296 GCST90235242 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin regulatory light chain 12A level in Chronic kidney disease with hypertension and no diabetes (19373_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin regulatory light chain MRLC3 in blood serum http://purl.obolibrary.org/obo/OBA_2042419 GCST90235243 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein p13 MTCP-1 level in Chronic kidney disease with hypertension and no diabetes (19374_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein p13 MTCP-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044592 GCST90235244 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EF-hand domain-containing protein D1 level in Chronic kidney disease with hypertension and no diabetes (19616_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EF-hand domain-containing protein D1 in blood serum http://purl.obolibrary.org/obo/OBA_2044288 GCST90235295 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disks large homolog 2 level in Chronic kidney disease with hypertension and no diabetes (19620_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disks large homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041309 GCST90235296 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activin A level in Chronic kidney disease with hypertension and no diabetes (19622_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of activin/inhibin beta A chain in blood serum http://purl.obolibrary.org/obo/OBA_2040209 GCST90235297 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein SA level in Chronic kidney disease with hypertension and no diabetes (19623_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 40s ribosomal protein SA measurement http://www.ebi.ac.uk/efo/EFO_0020119 GCST90235298 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-synuclein level in Chronic kidney disease with hypertension and no diabetes (19630_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-synuclein in blood serum http://purl.obolibrary.org/obo/OBA_2043567 GCST90235299 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HLA class I histocompatibility antigen, alpha chain G level in Chronic kidney disease with hypertension and no diabetes (19636_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MHC class I histocompatibility antigen, alpha chain G in blood serum http://purl.obolibrary.org/obo/OBA_2041882 GCST90235300 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynorphin A (1-17) level in Chronic kidney disease with hypertension and no diabetes (19638_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of proenkephalin-B in blood serum http://purl.obolibrary.org/obo/OBA_2042838 GCST90235301 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Islet amyloid polypeptide level in Chronic kidney disease with hypertension and no diabetes (19639_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of islet amyloid polypeptide in blood serum http://purl.obolibrary.org/obo/OBA_2041965 GCST90235302 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Parathyroid Hormone1-34 level in Chronic kidney disease with hypertension and no diabetes (19640_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of parathyroid hormone in blood serum http://purl.obolibrary.org/obo/OBA_2043094 GCST90235303 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Septin-5 level in Chronic kidney disease with hypertension and no diabetes (19742_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of septin-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043450 GCST90235304 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. V-set and transmembrane domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (19743_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of V-set and transmembrane domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044452 GCST90235305 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diphosphomevalonate decarboxylase level in Chronic kidney disease with hypertension and no diabetes (19748_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diphosphomevalonate decarboxylase in blood serum http://purl.obolibrary.org/obo/OBA_2042467 GCST90235306 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionine aminopeptidase 1D, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19752_197) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methionine aminopeptidase 1D, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042281 GCST90235307 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATPase inhibitor, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19755_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATPase inhibitor, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040735 GCST90235308 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-type lectin domain family 4 member G level in Chronic kidney disease with hypertension and no diabetes (19765_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-type lectin domain family 4 member G in blood serum http://purl.obolibrary.org/obo/OBA_2044270 GCST90235309 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystatin B level in Chronic kidney disease with hypertension and no diabetes (19768_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 cystatin B measurement http://www.ebi.ac.uk/efo/EFO_0010593 GCST90235310 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hemoglobin subunit gamma-2 level in Chronic kidney disease with hypertension and no diabetes (19774_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hemoglobin subunit gamma-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041841 GCST90235311 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Meprin A subunit alpha level in Chronic kidney disease with hypertension and no diabetes (19786_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of meprin A subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042339 GCST90235312 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proto-oncogene tyrosine-protein kinase MER level in Chronic kidney disease with hypertension and no diabetes (19787_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tyrosine-protein kinase Mer in blood serum http://purl.obolibrary.org/obo/OBA_2042340 GCST90235313 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uridine diphosphate glucose pyrophosphatase level in Chronic kidney disease with hypertension and no diabetes (19794_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of uridine diphosphate glucose pyrophosphatase NUDT14 in blood serum http://purl.obolibrary.org/obo/OBA_2042666 GCST90235314 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone acetyltransferase KAT2A level in Chronic kidney disease with hypertension and no diabetes (19797_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone acetyltransferase KAT2A in blood serum http://purl.obolibrary.org/obo/OBA_2041690 GCST90235315 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-binding cancer antigen expressed on SiSo cells level in Chronic kidney disease with hypertension and no diabetes (19802_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-binding cancer antigen expressed on SiSo cells in blood serum http://purl.obolibrary.org/obo/OBA_2041404 GCST90235316 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (19803_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinol-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043212 GCST90235317 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerase II subunit RPB9 level in Chronic kidney disease with hypertension and no diabetes (19809_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerase II subunit RPB9 in blood serum http://purl.obolibrary.org/obo/OBA_2042970 GCST90235318 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidoglycan recognition protein I-beta level in Chronic kidney disease with hypertension and no diabetes (19821_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidoglycan recognition protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042864 GCST90235319 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isoleucine--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (12815_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isoleucine--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2041966 GCST90233708 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein GEM level in Chronic kidney disease with hypertension and no diabetes (12817_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of GTP-binding protein GEM in blood serum http://purl.obolibrary.org/obo/OBA_2041701 GCST90233709 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Urea transporter 2 level in Chronic kidney disease with hypertension and no diabetes (12818_159) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of urea transporter 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043525 GCST90233710 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRB2-related adapter protein level in Chronic kidney disease with hypertension and no diabetes (12820_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GRB2-related adapter protein in blood serum http://purl.obolibrary.org/obo/OBA_2041782 GCST90233711 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NACHT, LRR and PYD domains-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (12821_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NACHT, LRR and PYD domains-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2042592 GCST90233712 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid beta A4 precursor protein-binding family B member 1 level in Chronic kidney disease with hypertension and no diabetes (12822_34) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233713 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DCC-interacting protein 13-alpha level in Chronic kidney disease with hypertension and no diabetes (12825_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DCC-interacting protein 13-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040632 GCST90233714 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium/iodide cotransporter level in Chronic kidney disease with hypertension and no diabetes (12826_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium/iodide cotransporter in blood serum http://purl.obolibrary.org/obo/OBA_2043538 GCST90233715 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 3 level in Chronic kidney disease with hypertension and no diabetes (12827_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043260 GCST90233716 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone deacetylase complex subunit SAP18 level in Chronic kidney disease with hypertension and no diabetes (12830_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone deacetylase complex subunit SAP18 in blood serum http://purl.obolibrary.org/obo/OBA_2043377 GCST90233717 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcineurin B homologous protein 3 level in Chronic kidney disease with hypertension and no diabetes (12831_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcineurin B homologous protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043829 GCST90233718 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Set1/Ash2 histone methyltransferase complex subunit ASH2 level in Chronic kidney disease with hypertension and no diabetes (12832_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Set1/Ash2 histone methyltransferase complex subunit ASH2 in blood serum http://purl.obolibrary.org/obo/OBA_2040699 GCST90233719 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Potassium voltage-gated channel subfamily F member 1 level in Chronic kidney disease with hypertension and no diabetes (12834_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-gated potassium channel KCNF1 in blood serum http://purl.obolibrary.org/obo/OBA_2040222 GCST90233720 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pyrin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (12835_101) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pyrin domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043125 GCST90233721 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 15 level in Chronic kidney disease with hypertension and no diabetes (12838_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 15 in blood serum http://purl.obolibrary.org/obo/OBA_2041380 GCST90233722 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-10 level in Chronic kidney disease with hypertension and no diabetes (12842_43) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of syntaxin-10 in blood serum http://purl.obolibrary.org/obo/OBA_2043708 GCST90233723 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 410 level in Chronic kidney disease with hypertension and no diabetes (12843_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 410 in blood serum http://purl.obolibrary.org/obo/OBA_2044205 GCST90233724 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BAG family molecular chaperone regulator 4 level in Chronic kidney disease with hypertension and no diabetes (12844_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BAG family molecular chaperone regulator 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040768 GCST90233725 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-17 level in Chronic kidney disease with hypertension and no diabetes (12845_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-17 in blood serum http://purl.obolibrary.org/obo/OBA_2043587 GCST90233726 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. F-box/LRR-repeat protein 5 level in Chronic kidney disease with hypertension and no diabetes (12846_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of F-box/LRR-repeat protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041557 GCST90233727 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. mRNA-capping enzyme level in Chronic kidney disease with hypertension and no diabetes (12847_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mRNA-capping enzyme in blood serum http://purl.obolibrary.org/obo/OBA_2043301 GCST90233728 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho guanine nucleotide exchange factor 2 level in Chronic kidney disease with hypertension and no diabetes (12848_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Rho guanine nucleotide exchange factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040660 GCST90233729 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GSK3-beta interaction protein level in Chronic kidney disease with hypertension and no diabetes (12849_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GSK3B-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2041798 GCST90233730 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed DNA/RNA polymerase mu level in Chronic kidney disease with hypertension and no diabetes (12851_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed DNA/RNA polymerase mu in blood serum http://purl.obolibrary.org/obo/OBA_2042965 GCST90233731 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomodulin-2 level in Chronic kidney disease with hypertension and no diabetes (12853_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tropomodulin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043878 GCST90233732 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional enhancer factor TEF-5 level in Chronic kidney disease with hypertension and no diabetes (12854_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional enhancer factor TEF-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043822 GCST90233733 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cas scaffolding protein family member 4 level in Chronic kidney disease with hypertension and no diabetes (12855_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Cas scaffolding protein family member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040907 GCST90233734 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 237 level in Chronic kidney disease with hypertension and no diabetes (12856_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 237 in blood serum http://purl.obolibrary.org/obo/OBA_2040578 GCST90233735 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Enoyl-CoA delta isomerase 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12859_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of enoyl-CoA Delta isomerase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042841 GCST90233736 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-regulated phosphoprotein 21 level in Chronic kidney disease with hypertension and no diabetes (12860_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-regulated phosphoprotein 21 in blood serum http://purl.obolibrary.org/obo/OBA_2040684 GCST90233737 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomodulin-3 level in Chronic kidney disease with hypertension and no diabetes (12861_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tropomodulin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043879 GCST90233738 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Enhancer of filamentation 1 level in Chronic kidney disease with hypertension and no diabetes (12862_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of enhancer of filamentation 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042552 GCST90233739 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Magnesium transporter NIPA4 level in Chronic kidney disease with hypertension and no diabetes (12864_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of magnesium transporter NIPA4 in blood serum http://purl.obolibrary.org/obo/OBA_2041967 GCST90233740 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynein light chain Tctex-type 3 level in Chronic kidney disease with hypertension and no diabetes (12867_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynein light chain Tctex-type 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041396 GCST90233741 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable ATP-dependent RNA helicase DDX6 level in Chronic kidney disease with hypertension and no diabetes (12869_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable ATP-dependent RNA helicase DDX6 in blood serum http://purl.obolibrary.org/obo/OBA_2044279 GCST90233742 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Twinfilin-1 level in Chronic kidney disease with hypertension and no diabetes (12871_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of twinfilin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043962 GCST90233743 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic nucleotide-gated olfactory channel level in Chronic kidney disease with hypertension and no diabetes (12872_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic nucleotide-gated olfactory channel in blood serum http://purl.obolibrary.org/obo/OBA_2040218 GCST90233744 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukosialin level in Chronic kidney disease with hypertension and no diabetes (12873_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leukosialin in blood serum http://purl.obolibrary.org/obo/OBA_2040347 GCST90233745 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (12875_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044432 GCST90233746 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm flagellar protein 1 level in Chronic kidney disease with hypertension and no diabetes (12876_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm flagellar protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043624 GCST90233747 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxysterol-binding protein-related protein 11 level in Chronic kidney disease with hypertension and no diabetes (12878_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxysterol-binding protein-related protein 11 in blood serum http://purl.obolibrary.org/obo/OBA_2042712 GCST90233748 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoblastoma-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (12879_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinoblastoma-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040197 GCST90233749 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptic vesicle glycoprotein 2A level in Chronic kidney disease with hypertension and no diabetes (12880_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptic vesicle glycoprotein 2A in blood serum http://purl.obolibrary.org/obo/OBA_2043739 GCST90233750 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol dehydrogenase 16 level in Chronic kidney disease with hypertension and no diabetes (12881_17) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of retinol dehydrogenase 16 in blood serum http://purl.obolibrary.org/obo/OBA_2043227 GCST90233751 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly [ADP-ribose] polymerase 11 level in Chronic kidney disease with hypertension and no diabetes (12882_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein mono-ADP-ribosyltransferase PARP11 in blood serum http://purl.obolibrary.org/obo/OBA_2042763 GCST90233752 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor subfamily 1 group D member 2 level in Chronic kidney disease with hypertension and no diabetes (12885_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor subfamily 1 group D member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042628 GCST90233753 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone deacetylase complex subunit SAP30 level in Chronic kidney disease with hypertension and no diabetes (12888_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of histone deacetylase complex subunit SAP30 in blood serum http://purl.obolibrary.org/obo/OBA_2043378 GCST90233754 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MICAL-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (12891_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MICAL-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042367 GCST90233755 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (12892_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043760 GCST90233756 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-interferon-inducible protein 16 level in Chronic kidney disease with hypertension and no diabetes (12893_159) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90233757 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD-dependent protein deacetylase sirtuin-1 level in Chronic kidney disease with hypertension and no diabetes (19823_75) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of NAD-dependent protein deacetylase sirtuin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043513 GCST90235320 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoplasmic aconitate hydratase level in Chronic kidney disease with hypertension and no diabetes (20054_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytoplasmic aconitate hydratase in blood serum http://purl.obolibrary.org/obo/OBA_2040479 GCST90235321 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinal dehydrogenase 2 level in Chronic kidney disease with hypertension and no diabetes (20055_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinal dehydrogenase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040559 GCST90235322 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-10 level in Chronic kidney disease with hypertension and no diabetes (20056_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90235323 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone chaperone ASF1B level in Chronic kidney disease with hypertension and no diabetes (20057_177) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone chaperone ASF1B in blood serum http://purl.obolibrary.org/obo/OBA_2040697 GCST90235324 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Frizzled-5 level in Chronic kidney disease with hypertension and no diabetes (20066_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of frizzled-5 in blood serum http://purl.obolibrary.org/obo/OBA_2041641 GCST90235325 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Factor seven-activating protease level in Chronic kidney disease with hypertension and no diabetes (20067_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hyaluronan-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041830 GCST90235326 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. G antigen 12F level in Chronic kidney disease with hypertension and no diabetes (20068_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of G antigen 12F in blood serum http://purl.obolibrary.org/obo/OBA_2044759 GCST90235327 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycine N-acyltransferase-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (20069_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycine N-acyltransferase-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041741 GCST90235328 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin-like protein KIF3B level in Chronic kidney disease with hypertension and no diabetes (24953_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kinesin-like protein KIF3B in blood serum http://purl.obolibrary.org/obo/OBA_2042100 GCST90236773 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-1 complex subunit beta-1 level in Chronic kidney disease with hypertension and no diabetes (24954_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-1 complex subunit beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040608 GCST90236774 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc fingers and homeoboxes protein 2 level in Chronic kidney disease with hypertension and no diabetes (24955_116) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc fingers and homeoboxes protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044185 GCST90236775 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N6-adenosine-methyltransferase 70 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (24956_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N6-adenosine-methyltransferase catalytic subunit in blood serum http://purl.obolibrary.org/obo/OBA_2042347 GCST90236776 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Espin level in Chronic kidney disease with hypertension and no diabetes (24957_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of espin in blood serum http://purl.obolibrary.org/obo/OBA_2041511 GCST90236777 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-binding protein RFX5 level in Chronic kidney disease with hypertension and no diabetes (24958_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-binding protein RFX5 in blood serum http://purl.obolibrary.org/obo/OBA_2043249 GCST90236778 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome b5 reductase 4 level in Chronic kidney disease with hypertension and no diabetes (24959_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome b5 reductase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041213 GCST90236779 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Huntingtin-interacting protein 1-related protein level in Chronic kidney disease with hypertension and no diabetes (24960_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of huntingtin-interacting protein 1-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2041877 GCST90236780 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 domain-containing kinase-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (24962_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH3 domain-containing kinase-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043495 GCST90236781 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-lymphoma invasion and metastasis-inducing protein 2 level in Chronic kidney disease with hypertension and no diabetes (24968_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho guanine nucleotide exchange factor TIAM2 in blood serum http://purl.obolibrary.org/obo/OBA_2043849 GCST90236782 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serrate RNA effector molecule homolog level in Chronic kidney disease with hypertension and no diabetes (24970_117) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serrate RNA effector molecule in blood serum http://purl.obolibrary.org/obo/OBA_2043660 GCST90236783 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositide phosphatase SAC2 level in Chronic kidney disease with hypertension and no diabetes (24971_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositide phosphatase SAC2 in blood serum http://purl.obolibrary.org/obo/OBA_2042032 GCST90236784 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MICAL-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (24973_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MICAL-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042366 GCST90236785 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fc receptor-like A level in Chronic kidney disease with hypertension and no diabetes (24975_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fc receptor-like A in blood serum http://purl.obolibrary.org/obo/OBA_2041566 GCST90236786 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Villin-like protein level in Chronic kidney disease with hypertension and no diabetes (24977_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of villin-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2044100 GCST90236787 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 3 subunit B level in Chronic kidney disease with hypertension and no diabetes (24979_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 3 subunit B in blood serum http://purl.obolibrary.org/obo/OBA_2041446 GCST90236788 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoplasmic dynein 1 light intermediate chain 1 level in Chronic kidney disease with hypertension and no diabetes (24981_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytoplasmic dynein 1 light intermediate chain 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041392 GCST90236789 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAGUK p55 subfamily member 5 level in Chronic kidney disease with hypertension and no diabetes (24982_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein PALS1 in blood serum http://purl.obolibrary.org/obo/OBA_2042406 GCST90236790 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ELKS/RAB6-interacting/CAST family member 1 level in Chronic kidney disease with hypertension and no diabetes (24983_119) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ELKS/Rab6-interacting/CAST family member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041501 GCST90236791 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-4 level in Chronic kidney disease with hypertension and no diabetes (2500_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiopoietin-4 measurement http://www.ebi.ac.uk/efo/EFO_0020147 GCST90236792 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-1 level in Chronic kidney disease with hypertension and no diabetes (2501_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020209 GCST90236793 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transitional endoplasmic reticulum ATPase level in Chronic kidney disease with hypertension and no diabetes (25033_194) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transitional endoplasmic reticulum ATPase in blood serum http://purl.obolibrary.org/obo/OBA_2044090 GCST90236794 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ran GTPase-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (25036_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ran GTPase-activating protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043192 GCST90236795 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aspartyl aminopeptidase level in Chronic kidney disease with hypertension and no diabetes (25037_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aspartyl aminopeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2041338 GCST90236796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Wee1-like protein kinase 2 level in Chronic kidney disease with hypertension and no diabetes (25038_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Wee1-like protein kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044129 GCST90236797 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (25039_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042124 GCST90236798 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4 level in Chronic kidney disease with hypertension and no diabetes (25041_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042853 GCST90236799 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD-dependent malic enzyme, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (25042_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NAD-dependent malic enzyme, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042323 GCST90236800 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Succinyl-CoA:3-ketoacid-coenzyme A transferase 1, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (25043_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of succinyl-CoA:3-ketoacid-coenzyme A transferase 1, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042726 GCST90236801 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C and casein kinase substrate in neurons protein 2 level in Chronic kidney disease with hypertension and no diabetes (25048_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein kinase C and casein kinase substrate in neurons protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042740 GCST90236802 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nonspecific lipid-transfer protein level in Chronic kidney disease with hypertension and no diabetes (25049_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90236803 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tripeptidyl-peptidase 2 level in Chronic kidney disease with hypertension and no diabetes (25050_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tripeptidyl-peptidase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043914 GCST90236804 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fat mass and obesity-associated protein level in Chronic kidney disease with hypertension and no diabetes (25051_104) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-ketoglutarate-dependent dioxygenase FTO in blood serum http://purl.obolibrary.org/obo/OBA_2041628 GCST90236805 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytokine receptor-like factor 3 level in Chronic kidney disease with hypertension and no diabetes (25052_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytokine receptor-like factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041148 GCST90236806 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytoplasmic dynein 1 light intermediate chain 2 level in Chronic kidney disease with hypertension and no diabetes (25053_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytoplasmic dynein 1 light intermediate chain 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041393 GCST90236807 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-mRNA-processing factor 19 level in Chronic kidney disease with hypertension and no diabetes (25054_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pre-mRNA-processing factor 19 in blood serum http://purl.obolibrary.org/obo/OBA_2043038 GCST90236808 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxysterol-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (25055_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oxysterol-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042711 GCST90236809 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-actinin-4 level in Chronic kidney disease with hypertension and no diabetes (25057_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-actinin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040491 GCST90236810 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Membrane-associated phosphatidylinositol transfer protein 3 level in Chronic kidney disease with hypertension and no diabetes (25058_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of membrane-associated phosphatidylinositol transfer protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042903 GCST90236811 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone deacetylase 6 level in Chronic kidney disease with hypertension and no diabetes (25059_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone deacetylase 6 in blood serum http://purl.obolibrary.org/obo/OBA_2041848 GCST90236812 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDNF family receptor alpha-3 level in Chronic kidney disease with hypertension and no diabetes (2505_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 gdnf family receptor alpha-3 measurement http://www.ebi.ac.uk/efo/EFO_0020401 GCST90236813 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nicotinamide N-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (19376_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nicotinamide N-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042603 GCST90235245 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noelin-2 level in Chronic kidney disease with hypertension and no diabetes (19377_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of noelin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042702 GCST90235246 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-3D level in Chronic kidney disease with hypertension and no diabetes (19379_154) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-3D in blood serum http://purl.obolibrary.org/obo/OBA_2043161 GCST90235247 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 21 level in Chronic kidney disease with hypertension and no diabetes (19381_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 21 in blood serum http://purl.obolibrary.org/obo/OBA_2043259 GCST90235248 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 2-interacting protein level in Chronic kidney disease with hypertension and no diabetes (19383_131) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 2-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2041032 GCST90235249 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-12 level in Chronic kidney disease with hypertension and no diabetes (19388_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 cadherin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020210 GCST90235250 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N(G),N(G)-dimethylarginine dimethylaminohydrolase 1 level in Chronic kidney disease with hypertension and no diabetes (19392_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N(G),N(G)-dimethylarginine dimethylaminohydrolase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041251 GCST90235251 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isoform L-VEGF165 level in Chronic kidney disease with hypertension and no diabetes (19437_61) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of vascular endothelial growth factor A in blood serum http://purl.obolibrary.org/obo/OBA_2044095 GCST90235252 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-mRNA-splicing factor SYF2 level in Chronic kidney disease with hypertension and no diabetes (19438_68) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pre-mRNA-splicing factor SYF2 in blood serum http://purl.obolibrary.org/obo/OBA_2043743 GCST90235253 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GMP reductase 2 level in Chronic kidney disease with hypertension and no diabetes (19446_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GMP reductase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041746 GCST90235254 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uridine phosphorylase 1 level in Chronic kidney disease with hypertension and no diabetes (19448_104) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uridine phosphorylase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044042 GCST90235255 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death protein 6 level in Chronic kidney disease with hypertension and no diabetes (19488_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of programmed cell death protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042814 GCST90235256 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kidney-associated antigen 1 level in Chronic kidney disease with hypertension and no diabetes (19492_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kidney-associated antigen 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042080 GCST90235257 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylneuraminate lyase level in Chronic kidney disease with hypertension and no diabetes (19496_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-acetylneuraminate lyase in blood serum http://purl.obolibrary.org/obo/OBA_2042614 GCST90235258 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-3 level in Chronic kidney disease with hypertension and no diabetes (19503_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043589 GCST90235259 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thymidylate kinase level in Chronic kidney disease with hypertension and no diabetes (19504_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thymidylate kinase in blood serum http://purl.obolibrary.org/obo/OBA_2041377 GCST90235260 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycine N-acyltransferase level in Chronic kidney disease with hypertension and no diabetes (19506_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycine N-acyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041740 GCST90235261 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DCN1-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (19511_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DCN1-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041247 GCST90235262 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High mobility group protein HMGI-C level in Chronic kidney disease with hypertension and no diabetes (19516_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of high mobility group protein HMGI-C in blood serum http://purl.obolibrary.org/obo/OBA_2041888 GCST90235263 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein DJ-1 level in Chronic kidney disease with hypertension and no diabetes (19523_215) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein dj-1 measurement http://www.ebi.ac.uk/efo/EFO_0020670 GCST90235264 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-1A level in Chronic kidney disease with hypertension and no diabetes (19553_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 syntaxin-1a measurement http://www.ebi.ac.uk/efo/EFO_0020759 GCST90235265 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small ubiquitin-related modifier 2 level in Chronic kidney disease with hypertension and no diabetes (19555_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of small ubiquitin-related modifier 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043734 GCST90235266 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement receptor type 1 level in Chronic kidney disease with hypertension and no diabetes (19556_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of complement receptor type 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040269 GCST90235267 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-klotho level in Chronic kidney disease with hypertension and no diabetes (19557_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of beta-klotho in blood serum http://purl.obolibrary.org/obo/OBA_2042115 GCST90235268 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Low-density lipoprotein receptor-related protein 4 level in Chronic kidney disease with hypertension and no diabetes (19558_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of low-density lipoprotein receptor-related protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042233 GCST90235269 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PAX-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (12894_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PAX-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042772 GCST90233758 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diacylglycerol kinase beta level in Chronic kidney disease with hypertension and no diabetes (12895_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diacylglycerol kinase beta in blood serum http://purl.obolibrary.org/obo/OBA_2041293 GCST90233759 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cubilin level in Chronic kidney disease with hypertension and no diabetes (12904_180) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cubilin in blood serum http://purl.obolibrary.org/obo/OBA_2041196 GCST90233760 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein p13 MTCP-1 level in Chronic kidney disease with hypertension and no diabetes (12916_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein p13 MTCP-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044592 GCST90233761 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type I cytoskeletal 17 level in Chronic kidney disease with hypertension and no diabetes (12923_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type I cytoskeletal 17 in blood serum http://purl.obolibrary.org/obo/OBA_2042140 GCST90233762 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ISG15--protein ligase HERC5 level in Chronic kidney disease with hypertension and no diabetes (12934_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of E3 ISG15--protein ligase HERC5 in blood serum http://purl.obolibrary.org/obo/OBA_2044240 GCST90233763 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinaldehyde-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (12936_38) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of retinaldehyde-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043278 GCST90233764 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerases I and III subunit RPAC1 level in Chronic kidney disease with hypertension and no diabetes (12939_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerases I and III subunit RPAC1 in blood serum http://purl.obolibrary.org/obo/OBA_2042966 GCST90233765 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldehyde dehydrogenase family 3 member B1 level in Chronic kidney disease with hypertension and no diabetes (12940_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldehyde dehydrogenase family 3 member B1 in blood serum http://purl.obolibrary.org/obo/OBA_2044532 GCST90233766 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisome proliferator-activated receptor alpha level in Chronic kidney disease with hypertension and no diabetes (12954_71) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of peroxisome proliferator-activated receptor alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042978 GCST90233767 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. KIF1-binding protein level in Chronic kidney disease with hypertension and no diabetes (12956_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of KIF-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2042152 GCST90233768 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome b-c1 complex subunit 7 level in Chronic kidney disease with hypertension and no diabetes (12957_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome b-c1 complex subunit 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044045 GCST90233769 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucokinase level in Chronic kidney disease with hypertension and no diabetes (12960_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hexokinase-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041688 GCST90233770 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein GPR107 level in Chronic kidney disease with hypertension and no diabetes (12963_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein GPR107 in blood serum http://purl.obolibrary.org/obo/OBA_2041774 GCST90233771 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine and glycine-rich protein 2 level in Chronic kidney disease with hypertension and no diabetes (12968_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine and glycine-rich protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041175 GCST90233772 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Double-stranded RNA-binding protein Staufen homolog 2 level in Chronic kidney disease with hypertension and no diabetes (12970_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of double-stranded RNA-binding protein Staufen homolog 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043697 GCST90233773 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type I cytoskeletal 20 level in Chronic kidney disease with hypertension and no diabetes (12975_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type I cytoskeletal 20 in blood serum http://purl.obolibrary.org/obo/OBA_2042142 GCST90233774 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vinexin b level in Chronic kidney disease with hypertension and no diabetes (12976_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vinexin in blood serum http://purl.obolibrary.org/obo/OBA_2043597 GCST90233775 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pre-mRNA-splicing factor RBM22 level in Chronic kidney disease with hypertension and no diabetes (12980_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pre-mRNA-splicing factor RBM22 in blood serum http://purl.obolibrary.org/obo/OBA_2043205 GCST90233776 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/arginine-rich splicing factor 7 level in Chronic kidney disease with hypertension and no diabetes (12987_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/arginine-rich splicing factor 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043480 GCST90233777 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein EWS level in Chronic kidney disease with hypertension and no diabetes (12988_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein EWS in blood serum http://purl.obolibrary.org/obo/OBA_2041523 GCST90233778 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase kinase kinase 3 level in Chronic kidney disease with hypertension and no diabetes (12990_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitogen-activated protein kinase kinase kinase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042288 GCST90233779 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cullin-9 level in Chronic kidney disease with hypertension and no diabetes (12991_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cullin-9 in blood serum http://purl.obolibrary.org/obo/OBA_2041200 GCST90233780 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear protein localization protein 4 homolog level in Chronic kidney disease with hypertension and no diabetes (12993_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear protein localization protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042615 GCST90233781 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epididymal-specific lipocalin-10 level in Chronic kidney disease with hypertension and no diabetes (13007_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epididymal-specific lipocalin-10 in blood serum http://purl.obolibrary.org/obo/OBA_2042173 GCST90233782 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin-A4 level in Chronic kidney disease with hypertension and no diabetes (19560_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of plexin-A4 in blood serum http://purl.obolibrary.org/obo/OBA_2042938 GCST90235270 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Plexin-D1 level in Chronic kidney disease with hypertension and no diabetes (19561_216) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of plexin-D1 in blood serum http://purl.obolibrary.org/obo/OBA_2042940 GCST90235271 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 28 level in Chronic kidney disease with hypertension and no diabetes (19562_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 28 in blood serum http://purl.obolibrary.org/obo/OBA_2044062 GCST90235272 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Seizure 6-like protein level in Chronic kidney disease with hypertension and no diabetes (19563_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of seizure 6-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2043471 GCST90235273 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 4 level in Chronic kidney disease with hypertension and no diabetes (19564_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon regulatory factor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040376 GCST90235274 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor receptor variant III level in Chronic kidney disease with hypertension and no diabetes (19567_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epidermal growth factor receptor in blood serum http://purl.obolibrary.org/obo/OBA_2041427 GCST90235275 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-15 level in Chronic kidney disease with hypertension and no diabetes (19568_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-15 in blood serum http://purl.obolibrary.org/obo/OBA_2040281 GCST90235276 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 8 level in Chronic kidney disease with hypertension and no diabetes (19570_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor 8 in blood serum http://purl.obolibrary.org/obo/OBA_2041575 GCST90235277 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CCAAT/enhancer-binding protein gamma level in Chronic kidney disease with hypertension and no diabetes (19572_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CCAAT/enhancer-binding protein gamma in blood serum http://purl.obolibrary.org/obo/OBA_2040984 GCST90235278 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integrin alpha-IIb: beta-3 complex level in Chronic kidney disease with hypertension and no diabetes (19574_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 integrin alpha-IIb: beta-3 complex measurement http://www.ebi.ac.uk/efo/EFO_0020479 GCST90235279 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Erythropoietin receptor level in Chronic kidney disease with hypertension and no diabetes (19575_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 erythropoietin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020364 GCST90235280 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Docking protein 2 level in Chronic kidney disease with hypertension and no diabetes (19578_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of docking protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041344 GCST90235281 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil defensin 1 level in Chronic kidney disease with hypertension and no diabetes (19579_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neutrophil defensin 1 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044900 GCST90235282 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 9 level in Chronic kidney disease with hypertension and no diabetes (19584_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 9 measurement http://www.ebi.ac.uk/efo/EFO_0020387 GCST90235283 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rab-3C level in Chronic kidney disease with hypertension and no diabetes (19586_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rab-3C in blood serum http://purl.obolibrary.org/obo/OBA_2043160 GCST90235284 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Importin subunit alpha-5 level in Chronic kidney disease with hypertension and no diabetes (19587_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of importin subunit alpha-5 in blood serum http://purl.obolibrary.org/obo/OBA_2042132 GCST90235285 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pulmonary surfactant-associated protein D level in Chronic kidney disease with hypertension and no diabetes (19590_46) 466 African American individuals NA Illumina [14870897] (imputed) 1 pulmonary surfactant-associated protein d measurement http://www.ebi.ac.uk/efo/EFO_0020693 GCST90235286 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor IIIB 90 kDa subunit level in Chronic kidney disease with hypertension and no diabetes (19596_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 transcription factor IIIb 90 kda subunit measurement http://www.ebi.ac.uk/efo/EFO_0020778 GCST90235287 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat and SOCS box protein 9 level in Chronic kidney disease with hypertension and no diabetes (19601_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat and SOCS box protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2040693 GCST90235288 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor jun-D level in Chronic kidney disease with hypertension and no diabetes (19602_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor JunD in blood serum http://purl.obolibrary.org/obo/OBA_2042078 GCST90235289 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Indian hedgehog protein level in Chronic kidney disease with hypertension and no diabetes (19606_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Indian hedgehog protein in blood serum http://purl.obolibrary.org/obo/OBA_2041998 GCST90235290 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD81 antigen level in Chronic kidney disease with hypertension and no diabetes (19612_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD81 molecule in blood serum http://purl.obolibrary.org/obo/OBA_2040946 GCST90235291 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol dehydrogenase 10 level in Chronic kidney disease with hypertension and no diabetes (19613_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinol dehydrogenase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043224 GCST90235292 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcobalamin-1 level in Chronic kidney disease with hypertension and no diabetes (19614_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transcobalamin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043815 GCST90235293 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytosolic 5'-nucleotidase 3A level in Chronic kidney disease with hypertension and no diabetes (19615_213) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytosolic 5'-nucleotidase 3A in blood serum http://purl.obolibrary.org/obo/OBA_2042650 GCST90235294 Genome-wide genotyping array 2022-04-05 34855049 Pasman JA 2021-12-02 Behav Genet www.ncbi.nlm.nih.gov/pubmed/34855049 Genetic Risk for Smoking: Disentangling Interplay Between Genes and Socioeconomic Status. Lifetime smoking 272,943 European or unknown ancestry cases, 226,795 European or unknown ancestry controls NA NR [1300000] 112 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90100569 Genome-wide genotyping array 2022-04-05 34855049 Pasman JA 2021-12-02 Behav Genet www.ncbi.nlm.nih.gov/pubmed/34855049 Genetic Risk for Smoking: Disentangling Interplay Between Genes and Socioeconomic Status. Educational attainment 451,800 European or unknown ancestry individuals NA NR [1300000] 276 educational attainment http://www.ebi.ac.uk/efo/EFO_0011015 GCST90100570 Genome-wide genotyping array 2022-04-05 34855049 Pasman JA 2021-12-02 Behav Genet www.ncbi.nlm.nih.gov/pubmed/34855049 Genetic Risk for Smoking: Disentangling Interplay Between Genes and Socioeconomic Status. Lifetime smoking (without educational attainment) 272,943 European or unknown ancestry cases, 226,795 European or unknown ancestry controls NA NR [1300000] 47 smoking status measurement http://www.ebi.ac.uk/efo/EFO_0006527 GCST90100571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carnitine O-acetyltransferase level in Chronic kidney disease with hypertension and no diabetes (12637_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carnitine O-acetyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2041129 GCST90233586 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-arrestin-1 level in Chronic kidney disease with hypertension and no diabetes (12643_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-arrestin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040685 GCST90233587 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribulose-phosphate 3-epimerase level in Chronic kidney disease with hypertension and no diabetes (12646_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribulose-phosphate 3-epimerase in blood serum http://purl.obolibrary.org/obo/OBA_2043316 GCST90233588 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase SETD2 level in Chronic kidney disease with hypertension and no diabetes (12647_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone-lysine N-methyltransferase SETD2 in blood serum http://purl.obolibrary.org/obo/OBA_2043469 GCST90233589 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Malate dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12649_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of malate dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042318 GCST90233590 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein G(k) subunit alpha level in Chronic kidney disease with hypertension and no diabetes (12650_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide-binding protein G(i) subunit alpha-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041748 GCST90233591 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. [Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12651_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of [pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042832 GCST90233592 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenosylhomocysteinase 2 level in Chronic kidney disease with hypertension and no diabetes (12652_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of S-adenosylhomocysteine hydrolase-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044356 GCST90233593 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase I isoform gamma-2 level in Chronic kidney disease with hypertension and no diabetes (12653_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of casein kinase I isoform gamma-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041172 GCST90233594 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-soluble NSF attachment protein level in Chronic kidney disease with hypertension and no diabetes (12655_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-soluble NSF attachment protein in blood serum http://purl.obolibrary.org/obo/OBA_2042509 GCST90233595 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin light chain 1 level in Chronic kidney disease with hypertension and no diabetes (12656_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of kinesin light chain 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042116 GCST90233596 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDP-L-fucose synthase level in Chronic kidney disease with hypertension and no diabetes (12657_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GDP-L-fucose synthetase in blood serum http://purl.obolibrary.org/obo/OBA_2043955 GCST90233597 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pantothenate kinase 3 level in Chronic kidney disease with hypertension and no diabetes (12658_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pantothenate kinase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042756 GCST90233598 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Obg-like ATPase 1 level in Chronic kidney disease with hypertension and no diabetes (12659_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of obg-like ATPase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042699 GCST90233599 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-aminobutyric acid receptor-associated protein-like 1 level in Chronic kidney disease with hypertension and no diabetes (12661_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-aminobutyric acid receptor-associated protein-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041648 GCST90233600 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (12662_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041406 GCST90233601 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thiosulfate sulfurtransferase level in Chronic kidney disease with hypertension and no diabetes (12663_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of thiosulfate sulfurtransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043954 GCST90233602 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 13 level in Chronic kidney disease with hypertension and no diabetes (12664_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein phosphatase non-receptor type 13 in blood serum http://purl.obolibrary.org/obo/OBA_2043101 GCST90233603 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD97 antigen level in Chronic kidney disease with hypertension and no diabetes (18881_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD97 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020250 GCST90235041 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calsyntenin-2 level in Chronic kidney disease with hypertension and no diabetes (18882_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calsyntenin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041057 GCST90235042 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Destrin level in Chronic kidney disease with hypertension and no diabetes (18883_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of destrin in blood serum http://purl.obolibrary.org/obo/OBA_2041371 GCST90235043 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 4 level in Chronic kidney disease with hypertension and no diabetes (18884_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044286 GCST90235044 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Down syndrome cell adhesion molecule-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (18886_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell adhesion molecule DSCAML1 in blood serum http://purl.obolibrary.org/obo/OBA_2041366 GCST90235045 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ectonucleoside triphosphate diphosphohydrolase 2 level in Chronic kidney disease with hypertension and no diabetes (18887_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ectonucleoside triphosphate diphosphohydrolase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041483 GCST90235046 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein 12 level in Chronic kidney disease with hypertension and no diabetes (18888_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fatty acid-binding protein 12 in blood serum http://purl.obolibrary.org/obo/OBA_2044449 GCST90235047 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neutrophil cytosol factor 2 level in Chronic kidney disease with hypertension and no diabetes (10047_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neutrophil cytosol factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042526 GCST90232818 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Core-binding factor subunit beta level in Chronic kidney disease with hypertension and no diabetes (10048_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of core-binding factor subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040910 GCST90232819 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Telomeric repeat-binding factor 1 level in Chronic kidney disease with hypertension and no diabetes (10049_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of telomeric repeat-binding factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043827 GCST90232820 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gigaxonin level in Chronic kidney disease with hypertension and no diabetes (10054_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of gigaxonin in blood serum http://purl.obolibrary.org/obo/OBA_2041669 GCST90232821 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein M1 level in Chronic kidney disease with hypertension and no diabetes (10056_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein M1 in blood serum http://purl.obolibrary.org/obo/OBA_2041609 GCST90232822 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UV excision repair protein RAD23 homolog A level in Chronic kidney disease with hypertension and no diabetes (10058_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UV excision repair protein RAD23 homolog A in blood serum http://purl.obolibrary.org/obo/OBA_2043180 GCST90232823 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase FANCL level in Chronic kidney disease with hypertension and no diabetes (10063_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase FANCL in blood serum http://purl.obolibrary.org/obo/OBA_2041548 GCST90232824 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative hydrolase RBBP9 level in Chronic kidney disease with hypertension and no diabetes (10064_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine hydrolase RBBP9 in blood serum http://purl.obolibrary.org/obo/OBA_2044651 GCST90232825 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 level in Chronic kidney disease with hypertension and no diabetes (10069_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042894 GCST90232826 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2 level in Chronic kidney disease with hypertension and no diabetes (10070_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042921 GCST90232827 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosyl-DNA phosphodiesterase 1 level in Chronic kidney disease with hypertension and no diabetes (10073_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosyl-DNA phosphodiesterase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043821 GCST90232828 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bromodomain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (10074_128) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bromodomain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040824 GCST90232829 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-CoA-binding domain-containing protein 6 level in Chronic kidney disease with hypertension and no diabetes (10075_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-CoA-binding domain-containing protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040475 GCST90232830 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-4 complex subunit mu-1 level in Chronic kidney disease with hypertension and no diabetes (10076_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-4 complex subunit mu-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040613 GCST90232831 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BAG family molecular chaperone regulator 3 level in Chronic kidney disease with hypertension and no diabetes (10078_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BAG family molecular chaperone regulator 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040767 GCST90232832 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Translation initiation factor eIF-2B subunit alpha level in Chronic kidney disease with hypertension and no diabetes (10080_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of translation initiation factor eIF-2B subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041440 GCST90232833 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-binding protein SATB2 level in Chronic kidney disease with hypertension and no diabetes (10081_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-binding protein SATB2 in blood serum http://purl.obolibrary.org/obo/OBA_2043388 GCST90232834 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurofilament light polypeptide level in Chronic kidney disease with hypertension and no diabetes (10082_251) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurofilament light polypeptide in blood serum http://purl.obolibrary.org/obo/OBA_2042554 GCST90232835 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Steroidogenic acute regulatory protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (10085_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of steroidogenic acute regulatory protein, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043691 GCST90232836 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cystathionine beta-synthase level in Chronic kidney disease with hypertension and no diabetes (10086_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cystathionine beta-synthase in blood serum http://purl.obolibrary.org/obo/OBA_2040919 GCST90232837 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-crystallin A chain level in Chronic kidney disease with hypertension and no diabetes (10087_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-crystallin A chain in blood serum http://purl.obolibrary.org/obo/OBA_2041154 GCST90232838 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenine phosphoribosyltransferase level in Chronic kidney disease with hypertension and no diabetes (10088_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adenine phosphoribosyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2040633 GCST90232839 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylserotonin O-methyltransferase-like protein level in Chronic kidney disease with hypertension and no diabetes (10089_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable bifunctional dTTP/UTP pyrophosphatase/methyltransferase protein in blood serum http://purl.obolibrary.org/obo/OBA_2040702 GCST90232840 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 SUMO-protein ligase PIAS4 level in Chronic kidney disease with hypertension and no diabetes (10342_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 E3 SUMO-protein ligase PIAS4 measurement http://www.ebi.ac.uk/efo/EFO_0021906 GCST90232841 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-10 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (10344_334) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-10 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0021890 GCST90232842 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycolipid transfer protein level in Chronic kidney disease with hypertension and no diabetes (12513_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycolipid transfer protein in blood serum http://purl.obolibrary.org/obo/OBA_2041737 GCST90233511 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA (guanine-N(7)-)-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (12514_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA (guanine-N(7)-)-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2042344 GCST90233512 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uridine-cytidine kinase 2 level in Chronic kidney disease with hypertension and no diabetes (12515_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uridine-cytidine kinase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044017 GCST90233513 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional enhancer factor TEF-3 level in Chronic kidney disease with hypertension and no diabetes (12516_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional enhancer factor TEF-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043823 GCST90233514 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Programmed cell death protein 5 level in Chronic kidney disease with hypertension and no diabetes (12517_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of programmed cell death protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042813 GCST90233515 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein polybromo-1 level in Chronic kidney disease with hypertension and no diabetes (12518_289) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein polybromo-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042774 GCST90233516 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 4 inhibitor C level in Chronic kidney disease with hypertension and no diabetes (12521_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 4 inhibitor C in blood serum http://purl.obolibrary.org/obo/OBA_2040971 GCST90233517 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UV excision repair protein RAD23 homolog B level in Chronic kidney disease with hypertension and no diabetes (12522_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UV excision repair protein RAD23 homolog B in blood serum http://purl.obolibrary.org/obo/OBA_2043181 GCST90233518 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diamine acetyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (12524_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thialysine N-epsilon-acetyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043386 GCST90233519 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thyroid hormone receptor alpha level in Chronic kidney disease with hypertension and no diabetes (12527_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thyroid hormone receptor alpha in blood serum http://purl.obolibrary.org/obo/OBA_2040444 GCST90233520 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATPase WRNIP1 level in Chronic kidney disease with hypertension and no diabetes (12528_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATPase WRNIP1 in blood serum http://purl.obolibrary.org/obo/OBA_2044143 GCST90233521 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive peptidyl-prolyl cis-trans isomerase FKBP6 level in Chronic kidney disease with hypertension and no diabetes (12529_32) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of peptidyl-prolyl cis-trans isomerase FKBP6 in blood serum http://purl.obolibrary.org/obo/OBA_2041591 GCST90233522 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinases regulatory subunit 1 level in Chronic kidney disease with hypertension and no diabetes (12530_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinases regulatory subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041039 GCST90233523 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endogenous retrovirus group V member 1 Env polyprotein level in Chronic kidney disease with hypertension and no diabetes (12531_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endogenous retrovirus group V member 1 Env polyprotein in blood serum http://purl.obolibrary.org/obo/OBA_2044558 GCST90233524 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 R1 level in Chronic kidney disease with hypertension and no diabetes (12532_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 R1 in blood serum http://purl.obolibrary.org/obo/OBA_2040952 GCST90233525 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytohesin-2 level in Chronic kidney disease with hypertension and no diabetes (12533_135) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytohesin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041218 GCST90233526 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-binding and coiled-coil domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (12534_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-binding and coiled-coil domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040877 GCST90233527 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA repair protein XRCC1 level in Chronic kidney disease with hypertension and no diabetes (12535_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA repair protein XRCC1 in blood serum http://purl.obolibrary.org/obo/OBA_2044152 GCST90233528 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myotubularin-related protein 6 level in Chronic kidney disease with hypertension and no diabetes (12536_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myotubularin-related protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2042453 GCST90233529 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcriptional activator protein Pur-alpha level in Chronic kidney disease with hypertension and no diabetes (12537_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcriptional activator protein Pur-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043116 GCST90233530 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho-related GTP-binding protein RhoG level in Chronic kidney disease with hypertension and no diabetes (12540_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho-related GTP-binding protein RhoG in blood serum http://purl.obolibrary.org/obo/OBA_2043267 GCST90233531 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 560 level in Chronic kidney disease with hypertension and no diabetes (12543_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 560 in blood serum http://purl.obolibrary.org/obo/OBA_2044208 GCST90233532 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Smoothelin level in Chronic kidney disease with hypertension and no diabetes (12546_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of smoothelin in blood serum http://purl.obolibrary.org/obo/OBA_2043561 GCST90233533 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related GTP-binding protein C level in Chronic kidney disease with hypertension and no diabetes (12548_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related GTP-binding protein C in blood serum http://purl.obolibrary.org/obo/OBA_2043342 GCST90233534 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hematopoietic prostaglandin D synthase level in Chronic kidney disease with hypertension and no diabetes (12549_33) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of glutathione-requiring prostaglandin D synthase in blood serum http://purl.obolibrary.org/obo/OBA_2043089 GCST90233535 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-crystallin B2 level in Chronic kidney disease with hypertension and no diabetes (10000_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-crystallin B2 in blood serum http://purl.obolibrary.org/obo/OBA_2041156 GCST90232793 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RAF proto-oncogene serine/threonine-protein kinase level in Chronic kidney disease with hypertension and no diabetes (10001_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RAF proto-oncogene serine/threonine-protein kinase in blood serum http://purl.obolibrary.org/obo/OBA_2040426 GCST90232794 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 41 level in Chronic kidney disease with hypertension and no diabetes (10003_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 41 in blood serum http://purl.obolibrary.org/obo/OBA_2044204 GCST90232795 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ETS domain-containing protein Elk-1 level in Chronic kidney disease with hypertension and no diabetes (10006_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ETS domain-containing protein Elk-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041466 GCST90232796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylyl cyclase-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (10008_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanylyl cyclase-activating protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041820 GCST90232797 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beclin-1 level in Chronic kidney disease with hypertension and no diabetes (10010_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beclin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040792 GCST90232798 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol polyphosphate 5-phosphatase OCRL-1 level in Chronic kidney disease with hypertension and no diabetes (10011_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol polyphosphate 5-phosphatase OCRL in blood serum http://purl.obolibrary.org/obo/OBA_2042690 GCST90232799 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SAM pointed domain-containing Ets transcription factor level in Chronic kidney disease with hypertension and no diabetes (10012_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SAM pointed domain-containing Ets transcription factor in blood serum http://purl.obolibrary.org/obo/OBA_2043623 GCST90232800 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein SNAI2 level in Chronic kidney disease with hypertension and no diabetes (10014_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein SNAI2 in blood serum http://purl.obolibrary.org/obo/OBA_2043562 GCST90232801 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Voltage-gated potassium channel subunit beta-2 level in Chronic kidney disease with hypertension and no diabetes (10015_119) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of voltage-gated potassium channel subunit beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042086 GCST90232802 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA polymerase eta level in Chronic kidney disease with hypertension and no diabetes (10022_207) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA polymerase eta in blood serum http://purl.obolibrary.org/obo/OBA_2042963 GCST90232803 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vitamin D3 receptor level in Chronic kidney disease with hypertension and no diabetes (10023_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vitamin D3 receptor in blood serum http://purl.obolibrary.org/obo/OBA_2044094 GCST90232804 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 4-hydroxy-2-oxoglutarate aldolase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (10024_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 4-hydroxy-2-oxoglutarate aldolase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044731 GCST90232805 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydrolipoyl dehydrogenase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (10025_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dihydrolipoyl dehydrogenase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041308 GCST90232806 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adenine DNA glycosylase level in Chronic kidney disease with hypertension and no diabetes (10030_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adenine DNA glycosylase MUTYH in blood serum http://purl.obolibrary.org/obo/OBA_2042466 GCST90232807 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity protein phosphatase 4 level in Chronic kidney disease with hypertension and no diabetes (10035_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity protein phosphatase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041388 GCST90232808 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc fingers and homeoboxes protein 3 level in Chronic kidney disease with hypertension and no diabetes (10036_201) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc fingers and homeoboxes protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044186 GCST90232809 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sialic acid-binding Ig-like lectin 12 level in Chronic kidney disease with hypertension and no diabetes (10037_98) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90232810 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Purine nucleoside phosphorylase level in Chronic kidney disease with hypertension and no diabetes (10039_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of purine nucleoside phosphorylase in blood serum http://purl.obolibrary.org/obo/OBA_2042611 GCST90232811 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor protein 63 level in Chronic kidney disease with hypertension and no diabetes (10040_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor protein 63 in blood serum http://purl.obolibrary.org/obo/OBA_2043906 GCST90232812 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatocyte nuclear factor 4-alpha level in Chronic kidney disease with hypertension and no diabetes (10041_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatocyte nuclear factor 4-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041901 GCST90232813 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase Sgk3 level in Chronic kidney disease with hypertension and no diabetes (10042_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase Sgk3 in blood serum http://purl.obolibrary.org/obo/OBA_2043484 GCST90232814 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bromodomain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (10043_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bromodomain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040825 GCST90232815 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cullin-3 level in Chronic kidney disease with hypertension and no diabetes (10045_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cullin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041198 GCST90232816 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Baculoviral IAP repeat-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (10046_55) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of baculoviral IAP repeat-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040801 GCST90232817 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase Itchy homolog level in Chronic kidney disease with hypertension and no diabetes (12551_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase Itchy in blood serum http://purl.obolibrary.org/obo/OBA_2040424 GCST90233536 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase VRK1 level in Chronic kidney disease with hypertension and no diabetes (12553_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase VRK1 in blood serum http://purl.obolibrary.org/obo/OBA_2044114 GCST90233537 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA repair protein RAD51 homolog 4 level in Chronic kidney disease with hypertension and no diabetes (12554_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA repair protein RAD51 homolog 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043183 GCST90233538 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 C level in Chronic kidney disease with hypertension and no diabetes (12556_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 C in blood serum http://purl.obolibrary.org/obo/OBA_2043991 GCST90233539 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein Nova-1 level in Chronic kidney disease with hypertension and no diabetes (12557_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein Nova-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042610 GCST90233540 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-associated and SH3 domain-containing protein B level in Chronic kidney disease with hypertension and no diabetes (12558_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-associated and SH3 domain-containing protein B in blood serum http://purl.obolibrary.org/obo/OBA_2043987 GCST90233541 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 5'(3')-deoxyribonucleotidase, cytosolic type level in Chronic kidney disease with hypertension and no diabetes (12560_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 5'(3')-deoxyribonucleotidase, cytosolic type in blood serum http://purl.obolibrary.org/obo/OBA_2042648 GCST90233542 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase N1 level in Chronic kidney disease with hypertension and no diabetes (12562_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase N1 in blood serum http://purl.obolibrary.org/obo/OBA_2042907 GCST90233543 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor alpha-induced protein 8 level in Chronic kidney disease with hypertension and no diabetes (12563_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tumor necrosis factor alpha-induced protein 8 in blood serum http://purl.obolibrary.org/obo/OBA_2043889 GCST90233544 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 60S ribosome subunit biogenesis protein NIP7 homolog level in Chronic kidney disease with hypertension and no diabetes (12564_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 60S ribosome subunit biogenesis protein NIP7 in blood serum http://purl.obolibrary.org/obo/OBA_2042582 GCST90233545 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like ECH-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (12568_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 kelch-like ECH-associated protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0022023 GCST90233546 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (12571_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040668 GCST90233547 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Embryonal Fyn-associated substrate level in Chronic kidney disease with hypertension and no diabetes (12572_236) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of embryonal Fyn-associated substrate in blood serum http://purl.obolibrary.org/obo/OBA_2041423 GCST90233548 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tripartite motif-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (12573_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tripartite motif-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044373 GCST90233549 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Endothelin-2 level in Chronic kidney disease with hypertension and no diabetes (12574_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endothelin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041414 GCST90233550 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-1-tetrahydrofolate synthase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (12575_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-1-tetrahydrofolate synthase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2042448 GCST90233551 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoma-associated antigen 3 level in Chronic kidney disease with hypertension and no diabetes (12576_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoma-associated antigen 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042265 GCST90233552 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Flap endonuclease 1 level in Chronic kidney disease with hypertension and no diabetes (12577_100) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of flap endonuclease 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041571 GCST90233553 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor 3 level in Chronic kidney disease with hypertension and no diabetes (12578_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040640 GCST90233554 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-5 level in Chronic kidney disease with hypertension and no diabetes (12580_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit beta type-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043070 GCST90233555 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inositol monophosphatase 2 level in Chronic kidney disease with hypertension and no diabetes (12581_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol monophosphatase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042022 GCST90233556 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase A-Raf level in Chronic kidney disease with hypertension and no diabetes (12583_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase A-Raf in blood serum http://purl.obolibrary.org/obo/OBA_2040636 GCST90233557 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA excision repair protein ERCC-1 level in Chronic kidney disease with hypertension and no diabetes (12585_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA excision repair protein ERCC-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041502 GCST90233558 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (12587_65) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ADP-ribosylation factor-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040666 GCST90233559 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oligophrenin-1 level in Chronic kidney disease with hypertension and no diabetes (12591_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of oligophrenin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042708 GCST90233560 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. p53 and DNA damage-regulated protein 1 level in Chronic kidney disease with hypertension and no diabetes (12593_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of p53 and DNA damage-regulated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042837 GCST90233561 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Grancalcin level in Chronic kidney disease with hypertension and no diabetes (12594_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of grancalcin in blood serum http://purl.obolibrary.org/obo/OBA_2041684 GCST90233562 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomodulin-1 level in Chronic kidney disease with hypertension and no diabetes (12595_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tropomodulin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043877 GCST90233563 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Autophagy protein 5 level in Chronic kidney disease with hypertension and no diabetes (12597_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of autophagy protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040721 GCST90233564 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polyadenylate-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (12603_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polyadenylate-binding protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042735 GCST90233565 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polycomb protein SCMH1 level in Chronic kidney disease with hypertension and no diabetes (12604_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polycomb protein SCMH1 in blood serum http://purl.obolibrary.org/obo/OBA_2043403 GCST90233566 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Exosome complex component RRP40 level in Chronic kidney disease with hypertension and no diabetes (12605_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of exosome complex component RRP40 in blood serum http://purl.obolibrary.org/obo/OBA_2041526 GCST90233567 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-1 level in Chronic kidney disease with hypertension and no diabetes (12612_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit beta type-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043067 GCST90233568 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear receptor-binding protein level in Chronic kidney disease with hypertension and no diabetes (12616_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear receptor-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2042636 GCST90233569 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase 24 level in Chronic kidney disease with hypertension and no diabetes (12617_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase 24 in blood serum http://purl.obolibrary.org/obo/OBA_2040410 GCST90233570 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldo-keto reductase family 1 member C1 level in Chronic kidney disease with hypertension and no diabetes (12618_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member C1 in blood serum http://purl.obolibrary.org/obo/OBA_2040549 GCST90233571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1A level in Chronic kidney disease with hypertension and no diabetes (12619_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1A in blood serum http://purl.obolibrary.org/obo/OBA_2042991 GCST90233572 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Septin-11 level in Chronic kidney disease with hypertension and no diabetes (12620_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of septin-11 in blood serum http://purl.obolibrary.org/obo/OBA_2043448 GCST90233573 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform level in Chronic kidney disease with hypertension and no diabetes (12621_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform in blood serum http://purl.obolibrary.org/obo/OBA_2043007 GCST90233574 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone-lysine N-methyltransferase ASH1L level in Chronic kidney disease with hypertension and no diabetes (12622_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone-lysine N-methyltransferase ASH1L in blood serum http://purl.obolibrary.org/obo/OBA_2044490 GCST90233575 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Jumonji level in Chronic kidney disease with hypertension and no diabetes (12623_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Jumonji in blood serum http://purl.obolibrary.org/obo/OBA_2042069 GCST90233576 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 7 level in Chronic kidney disease with hypertension and no diabetes (12625_138) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042125 GCST90233577 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sentrin-specific protease 7 level in Chronic kidney disease with hypertension and no diabetes (12626_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sentrin-specific protease 7 in blood serum http://purl.obolibrary.org/obo/OBA_2043441 GCST90233578 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LanC-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (12628_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LanC-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042162 GCST90233579 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arfaptin-2 level in Chronic kidney disease with hypertension and no diabetes (12630_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arfaptin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040647 GCST90233580 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arylamine N-acetyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (12632_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of arylamine N-acetyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042514 GCST90233581 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein phosphatase non-receptor type 9 level in Chronic kidney disease with hypertension and no diabetes (12633_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein phosphatase non-receptor type 9 in blood serum http://purl.obolibrary.org/obo/OBA_2043104 GCST90233582 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Breast cancer anti-estrogen resistance protein 3 level in Chronic kidney disease with hypertension and no diabetes (12634_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 breast cancer anti-estrogen resistance protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0008040 GCST90233583 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. tRNA (cytosine(38)-C(5))-methyltransferase level in Chronic kidney disease with hypertension and no diabetes (12635_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tRNA (cytosine-5-)-methyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2043925 GCST90233584 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-lysine methyltransferase SMYD2 level in Chronic kidney disease with hypertension and no diabetes (12636_113) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of N-lysine methyltransferase SMYD2 in blood serum http://purl.obolibrary.org/obo/OBA_2044711 GCST90233585 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal transducer and activator of transcription 3 level in Chronic kidney disease with hypertension and no diabetes (10346_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 signal transducer and activator of transcription 3 measurement http://www.ebi.ac.uk/efo/EFO_0021907 GCST90232843 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 1 level in Chronic kidney disease with hypertension and no diabetes (10351_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon regulatory factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0021908 GCST90232844 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal transducer and activator of transcription 3 level in Chronic kidney disease with hypertension and no diabetes (10354_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 signal transducer and activator of transcription 3 measurement http://www.ebi.ac.uk/efo/EFO_0021907 GCST90232845 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor AP-1 level in Chronic kidney disease with hypertension and no diabetes (10356_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 transcription factor AP-1 measurement http://www.ebi.ac.uk/efo/EFO_0021909 GCST90232846 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 2'-5'-oligoadenylate synthase 1 level in Chronic kidney disease with hypertension and no diabetes (10361_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 2'-5'-oligoadenylate synthase 1 measurement http://www.ebi.ac.uk/efo/EFO_0021911 GCST90232847 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myc proto-oncogene protein level in Chronic kidney disease with hypertension and no diabetes (10362_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 myc proto-oncogene protein measurement http://www.ebi.ac.uk/efo/EFO_0021912 GCST90232848 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mothers against decapentaplegic homolog 3 level in Chronic kidney disease with hypertension and no diabetes (10363_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 mothers against decapentaplegic homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0021913 GCST90232849 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mothers against decapentaplegic homolog 2 level in Chronic kidney disease with hypertension and no diabetes (10364_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 mothers against decapentaplegic homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0021914 GCST90232850 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-23 level in Chronic kidney disease with hypertension and no diabetes (10365_132) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-23 measurement http://www.ebi.ac.uk/efo/EFO_0020501 GCST90232851 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-derived growth factor receptor alpha level in Chronic kidney disease with hypertension and no diabetes (10366_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 platelet-derived growth factor receptor alpha measurement http://www.ebi.ac.uk/efo/EFO_0021844 GCST90232852 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-12 level in Chronic kidney disease with hypertension and no diabetes (10367_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-12 measurement http://www.ebi.ac.uk/efo/EFO_0802654 GCST90232853 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal transducer and activator of transcription 1-alpha/beta level in Chronic kidney disease with hypertension and no diabetes (10370_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 signal transducer and activator of transcription 1-alpha/beta measurement http://www.ebi.ac.uk/efo/EFO_0021915 GCST90232854 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal transducer and activator of transcription 6 level in Chronic kidney disease with hypertension and no diabetes (10372_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 signal transducer and activator of transcription 6 measurement http://www.ebi.ac.uk/efo/EFO_0021916 GCST90232855 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (10382_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiopoietin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020148 GCST90232856 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase ZNRF3 level in Chronic kidney disease with hypertension and no diabetes (10390_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 E3 ubiquitin-protein ligase ZNRF3 measurement http://www.ebi.ac.uk/efo/EFO_0021943 GCST90232857 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Angiopoietin-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (10391_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 angiopoietin-related protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020148 GCST90232858 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Induced myeloid leukemia cell differentiation protein Mcl-1 level in Chronic kidney disease with hypertension and no diabetes (10396_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 induced myeloid leukemia cell differentiation protein Mcl-1 measurement http://www.ebi.ac.uk/efo/EFO_0021910 GCST90232859 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-12 level in Chronic kidney disease with hypertension and no diabetes (10418_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-12 in blood serum http://purl.obolibrary.org/obo/OBA_2043709 GCST90232860 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor class A member 5 level in Chronic kidney disease with hypertension and no diabetes (10419_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of scavenger receptor class A member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043392 GCST90232861 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fas apoptotic inhibitory molecule 1 level in Chronic kidney disease with hypertension and no diabetes (10420_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fas apoptotic inhibitory molecule 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041545 GCST90232862 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neural proliferation differentiation and control protein 1 level in Chronic kidney disease with hypertension and no diabetes (10424_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neural proliferation differentiation and control protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042612 GCST90232863 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4-galactosyltransferase 5 level in Chronic kidney disease with hypertension and no diabetes (10425_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,4-galactosyltransferase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040759 GCST90232864 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COMM domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (12509_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of COMM domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041090 GCST90233508 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal-transducing adaptor protein 1 level in Chronic kidney disease with hypertension and no diabetes (12510_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal-transducing adaptor protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043690 GCST90233509 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Solute carrier family 41 member 2 level in Chronic kidney disease with hypertension and no diabetes (12511_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of solute carrier family 41 member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043536 GCST90233510 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metallophosphoesterase MPPED2 level in Chronic kidney disease with hypertension and no diabetes (19153_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of metallophosphoesterase MPPED2 in blood serum http://purl.obolibrary.org/obo/OBA_2044442 GCST90235123 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glia-derived nexin level in Chronic kidney disease with hypertension and no diabetes (19154_41) 466 African American individuals NA Illumina [14870897] (imputed) 1 glia-derived nexin measurement http://www.ebi.ac.uk/efo/EFO_0020403 GCST90235124 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PCNA-associated factor level in Chronic kidney disease with hypertension and no diabetes (19158_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of PCNA-associated factor in blood serum http://purl.obolibrary.org/obo/OBA_2042744 GCST90235125 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA polymerase delta subunit 4 level in Chronic kidney disease with hypertension and no diabetes (19159_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA polymerase delta subunit 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042960 GCST90235126 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin carboxyl-terminal hydrolase 15 level in Chronic kidney disease with hypertension and no diabetes (19161_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin carboxyl-terminal hydrolase 15 in blood serum http://purl.obolibrary.org/obo/OBA_2044057 GCST90235127 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 59 level in Chronic kidney disease with hypertension and no diabetes (19163_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 59 in blood serum http://purl.obolibrary.org/obo/OBA_2044327 GCST90235128 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S19 level in Chronic kidney disease with hypertension and no diabetes (19166_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 40S ribosomal protein S19 in blood serum http://purl.obolibrary.org/obo/OBA_2043332 GCST90235129 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proline-serine-threonine phosphatase-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (19168_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proline-serine-threonine phosphatase-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043085 GCST90235130 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acidic fibroblast growth factor intracellular-binding protein level in Chronic kidney disease with hypertension and no diabetes (19169_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acidic fibroblast growth factor intracellular-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2041583 GCST90235131 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA polymerase epsilon subunit 3 level in Chronic kidney disease with hypertension and no diabetes (19170_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA polymerase epsilon subunit 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042962 GCST90235132 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AN1-type zinc finger protein 1 level in Chronic kidney disease with hypertension and no diabetes (19173_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AN1-type zinc finger protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044177 GCST90235133 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Golgin subfamily A member 7 level in Chronic kidney disease with hypertension and no diabetes (19174_141) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of golgin subfamily A member 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041761 GCST90235134 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MARCKS-related protein level in Chronic kidney disease with hypertension and no diabetes (19175_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of MARCKS-related protein in blood serum http://purl.obolibrary.org/obo/OBA_2042299 GCST90235135 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM49B level in Chronic kidney disease with hypertension and no diabetes (19176_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CYFIP-related Rac1 interactor B in blood serum http://purl.obolibrary.org/obo/OBA_2044296 GCST90235136 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EF-hand calcium-binding domain-containing protein 4B level in Chronic kidney disease with hypertension and no diabetes (24304_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EF-hand calcium-binding domain-containing protein 4B in blood serum http://purl.obolibrary.org/obo/OBA_2044429 GCST90236581 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysine-specific demethylase 8 level in Chronic kidney disease with hypertension and no diabetes (24307_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional peptidase and arginyl-hydroxylase JMJD5 in blood serum http://purl.obolibrary.org/obo/OBA_2044597 GCST90236582 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (24309_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043761 GCST90236583 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trafficking protein particle complex subunit 13 level in Chronic kidney disease with hypertension and no diabetes (24314_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trafficking protein particle complex subunit 13 in blood serum http://purl.obolibrary.org/obo/OBA_2044881 GCST90236584 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable methyltransferase BMT2 homolog level in Chronic kidney disease with hypertension and no diabetes (24316_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of S-adenosylmethionine sensor upstream of mTORC1 in blood serum http://purl.obolibrary.org/obo/OBA_2044882 GCST90236585 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. D-ribitol-5-phosphate cytidylyltransferase level in Chronic kidney disease with hypertension and no diabetes (24319_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of D-ribitol-5-phosphate cytidylyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044509 GCST90236586 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cathepsin G level in Chronic kidney disease with hypertension and no diabetes (2431_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 cathepsin G measurement http://www.ebi.ac.uk/efo/EFO_0020242 GCST90236587 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tripartite motif-containing protein 72 level in Chronic kidney disease with hypertension and no diabetes (24320_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tripartite motif-containing protein 72 in blood serum http://purl.obolibrary.org/obo/OBA_2044391 GCST90236588 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear prelamin A recognition factor level in Chronic kidney disease with hypertension and no diabetes (24321_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear prelamin A recognition factor in blood serum http://purl.obolibrary.org/obo/OBA_2042512 GCST90236589 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. General transcription factor IIE subunit 1 level in Chronic kidney disease with hypertension and no diabetes (24322_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of general transcription factor IIE subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041814 GCST90236590 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BRO1 domain-containing protein BROX level in Chronic kidney disease with hypertension and no diabetes (24323_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BRO1 domain-containing protein BROX in blood serum http://purl.obolibrary.org/obo/OBA_2044514 GCST90236591 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. D-amino-acid oxidase level in Chronic kidney disease with hypertension and no diabetes (19120_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of D-amino-acid oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2041227 GCST90235098 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquilin-2 level in Chronic kidney disease with hypertension and no diabetes (19121_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquilin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2044012 GCST90235099 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin regulatory light chain 12B level in Chronic kidney disease with hypertension and no diabetes (19122_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin regulatory light chain 12B in blood serum http://purl.obolibrary.org/obo/OBA_2042484 GCST90235100 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NF-kappa-B inhibitor delta level in Chronic kidney disease with hypertension and no diabetes (19123_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NF-kappa-B inhibitor delta in blood serum http://purl.obolibrary.org/obo/OBA_2042573 GCST90235101 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-like domain-containing CTD phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (19124_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-like domain-containing CTD phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044011 GCST90235102 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-dependent protein kinase type II-alpha regulatory subunit level in Chronic kidney disease with hypertension and no diabetes (19125_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-dependent protein kinase type II-alpha regulatory subunit in blood serum http://purl.obolibrary.org/obo/OBA_2043028 GCST90235103 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulation of nuclear pre-mRNA domain-containing protein 1B level in Chronic kidney disease with hypertension and no diabetes (19126_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulation of nuclear pre-mRNA domain-containing protein 1B in blood serum http://purl.obolibrary.org/obo/OBA_2044513 GCST90235104 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock protein beta-6 level in Chronic kidney disease with hypertension and no diabetes (19127_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock protein beta-6 in blood serum http://purl.obolibrary.org/obo/OBA_2041951 GCST90235105 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methenyltetrahydrofolate synthase domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (19129_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methenyltetrahydrofolate synthase domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2044481 GCST90235106 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serpin B8 level in Chronic kidney disease with hypertension and no diabetes (19130_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serpin B8 in blood serum http://purl.obolibrary.org/obo/OBA_2043463 GCST90235107 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nucleolysin TIAR level in Chronic kidney disease with hypertension and no diabetes (19131_184) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nucleolysin TIAR in blood serum http://purl.obolibrary.org/obo/OBA_2043847 GCST90235108 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 39S ribosomal protein L2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19132_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 39S ribosomal protein L2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042425 GCST90235109 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA-directed RNA polymerases I, II, and III subunit RPABC4 level in Chronic kidney disease with hypertension and no diabetes (19134_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA-directed RNA polymerases I, II, and III subunit RPABC4 in blood serum http://purl.obolibrary.org/obo/OBA_2042971 GCST90235110 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 7-methylguanosine phosphate-specific 5'-nucleotidase level in Chronic kidney disease with hypertension and no diabetes (19135_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 7-methylguanosine phosphate-specific 5'-nucleotidase in blood serum http://purl.obolibrary.org/obo/OBA_2042651 GCST90235111 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19136_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methylmalonate-semialdehyde dehydrogenase [acylating], mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2040565 GCST90235112 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock factor 2-binding protein level in Chronic kidney disease with hypertension and no diabetes (19139_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock factor 2-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2041942 GCST90235113 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Death-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (19141_22) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of death-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041228 GCST90235114 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA (cytosine-5)-methyltransferase 3-like level in Chronic kidney disease with hypertension and no diabetes (19142_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA (cytosine-5)-methyltransferase 3-like in blood serum http://purl.obolibrary.org/obo/OBA_2041337 GCST90235115 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH-cytochrome b5 reductase 2 level in Chronic kidney disease with hypertension and no diabetes (19143_38) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of NADH-cytochrome b5 reductase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041211 GCST90235116 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor 4 level in Chronic kidney disease with hypertension and no diabetes (19144_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043812 GCST90235117 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanoregulin level in Chronic kidney disease with hypertension and no diabetes (19145_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanoregulin in blood serum http://purl.obolibrary.org/obo/OBA_2042416 GCST90235118 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Galactoside-binding soluble lectin 13 level in Chronic kidney disease with hypertension and no diabetes (19147_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of galactoside-binding soluble lectin 13 in blood serum http://purl.obolibrary.org/obo/OBA_2042190 GCST90235119 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit Tim8 A level in Chronic kidney disease with hypertension and no diabetes (19148_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import inner membrane translocase subunit Tim8 A in blood serum http://purl.obolibrary.org/obo/OBA_2044368 GCST90235120 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoribosyl pyrophosphate synthase-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (19150_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoribosyl pyrophosphate synthase-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043042 GCST90235121 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase inhibitor 2 level in Chronic kidney disease with hypertension and no diabetes (19152_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase inhibitor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043003 GCST90235122 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 16 level in Chronic kidney disease with hypertension and no diabetes (2436_49) 466 African American individuals NA Illumina [14870897] (imputed) 1 C-X-C motif chemokine 16 measurement http://www.ebi.ac.uk/efo/EFO_0010911 GCST90236592 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin-like protein KIF3C level in Chronic kidney disease with hypertension and no diabetes (24407_31) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of kinesin-like protein KIF3C in blood serum http://purl.obolibrary.org/obo/OBA_2042101 GCST90236593 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Muscleblind-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (24408_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of muscleblind-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042309 GCST90236594 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinol dehydrogenase 13 level in Chronic kidney disease with hypertension and no diabetes (24409_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of retinol dehydrogenase 13 in blood serum http://purl.obolibrary.org/obo/OBA_2043226 GCST90236595 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase LRSAM1 level in Chronic kidney disease with hypertension and no diabetes (24411_144) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase LRSAM1 in blood serum http://purl.obolibrary.org/obo/OBA_2042239 GCST90236596 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptonemal complex central element protein 1-like level in Chronic kidney disease with hypertension and no diabetes (24412_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptonemal complex central element protein 1-like in blood serum http://purl.obolibrary.org/obo/OBA_2044749 GCST90236597 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peroxisomal coenzyme A diphosphatase NUDT7 level in Chronic kidney disease with hypertension and no diabetes (24413_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxisomal coenzyme A diphosphatase NUDT7 in blood serum http://purl.obolibrary.org/obo/OBA_2042673 GCST90236598 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Staphylococcal nuclease domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (24416_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of staphylococcal nuclease domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043568 GCST90236599 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rab GTPase-binding effector protein 1 level in Chronic kidney disease with hypertension and no diabetes (24417_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rab GTPase-binding effector protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043173 GCST90236600 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein HMX3 level in Chronic kidney disease with hypertension and no diabetes (24418_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein HMX3 in blood serum http://purl.obolibrary.org/obo/OBA_2041897 GCST90236601 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Molybdenum cofactor sulfurase level in Chronic kidney disease with hypertension and no diabetes (24419_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of molybdenum cofactor sulfurase in blood serum http://purl.obolibrary.org/obo/OBA_2042398 GCST90236602 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 10 level in Chronic kidney disease with hypertension and no diabetes (2441_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 10 measurement http://www.ebi.ac.uk/efo/EFO_0020376 GCST90236603 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deoxyhypusine hydroxylase level in Chronic kidney disease with hypertension and no diabetes (24420_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deoxyhypusine hydroxylase in blood serum http://purl.obolibrary.org/obo/OBA_2041342 GCST90236604 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spermatogenesis-associated protein 24 level in Chronic kidney disease with hypertension and no diabetes (24422_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spermatogenesis-associated protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2044771 GCST90236605 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1 regulatory subunit 3G level in Chronic kidney disease with hypertension and no diabetes (24423_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1 regulatory subunit 3G in blood serum http://purl.obolibrary.org/obo/OBA_2044389 GCST90236606 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TBC1 domain family member 25 level in Chronic kidney disease with hypertension and no diabetes (24424_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TBC1 domain family member 25 in blood serum http://purl.obolibrary.org/obo/OBA_2043787 GCST90236607 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methionyl-tRNA synthetase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (24425_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methionine--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2042301 GCST90236608 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catenin alpha-1 level in Chronic kidney disease with hypertension and no diabetes (24426_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of catenin alpha-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041186 GCST90236609 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catenin alpha-1 level in Chronic kidney disease with hypertension and no diabetes (24426_191) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of catenin alpha-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041186 GCST90236610 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Type II inositol-3,4-bisphosphate 4-phosphatase level in Chronic kidney disease with hypertension and no diabetes (24427_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol polyphosphate 4-phosphatase type II in blood serum http://purl.obolibrary.org/obo/OBA_2042030 GCST90236611 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysophospholipase D GDPD1 level in Chronic kidney disease with hypertension and no diabetes (24428_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysophospholipase D GDPD1 in blood serum http://purl.obolibrary.org/obo/OBA_2044776 GCST90236612 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 580 level in Chronic kidney disease with hypertension and no diabetes (24430_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 580 in blood serum http://purl.obolibrary.org/obo/OBA_2044210 GCST90236613 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (24431_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044421 GCST90236614 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRIP1-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (24432_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GRIP1-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041792 GCST90236615 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phytanoyl-CoA hydroxylase-interacting protein level in Chronic kidney disease with hypertension and no diabetes (24434_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phytanoyl-CoA hydroxylase-interacting protein in blood serum http://purl.obolibrary.org/obo/OBA_2042882 GCST90236616 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sharpin level in Chronic kidney disease with hypertension and no diabetes (24472_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sharpin in blood serum http://purl.obolibrary.org/obo/OBA_2043499 GCST90236642 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cancer/testis antigen family 45 member A3 level in Chronic kidney disease with hypertension and no diabetes (24473_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cancer/testis antigen family 45 member A3 in blood serum http://purl.obolibrary.org/obo/OBA_2041180 GCST90236643 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 9A level in Chronic kidney disease with hypertension and no diabetes (24474_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tetratricopeptide repeat protein 9A in blood serum http://purl.obolibrary.org/obo/OBA_2044791 GCST90236644 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-12 level in Chronic kidney disease with hypertension and no diabetes (24475_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-12 in blood serum http://purl.obolibrary.org/obo/OBA_2043584 GCST90236645 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Activating signal cointegrator 1 complex subunit 2 level in Chronic kidney disease with hypertension and no diabetes (24476_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of activating signal cointegrator 1 complex subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040695 GCST90236646 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 225B level in Chronic kidney disease with hypertension and no diabetes (24479_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 225B (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044898 GCST90236647 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Group IIE secretory phospholipase A2 level in Chronic kidney disease with hypertension and no diabetes (2447_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 group IIe secretory phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020424 GCST90236648 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. B-cell lymphoma/leukemia 11A level in Chronic kidney disease with hypertension and no diabetes (24486_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of B-cell lymphoma/leukemia 11A in blood serum http://purl.obolibrary.org/obo/OBA_2040788 GCST90236649 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biogenesis of lysosome-related organelles complex 1 subunit 3 level in Chronic kidney disease with hypertension and no diabetes (24487_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of biogenesis of lysosome-related organelles complex 1 subunit 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040807 GCST90236650 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein HID1 level in Chronic kidney disease with hypertension and no diabetes (24488_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein HID1 in blood serum http://purl.obolibrary.org/obo/OBA_2044838 GCST90236651 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor HES-3 level in Chronic kidney disease with hypertension and no diabetes (24489_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor HES-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041861 GCST90236652 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. THAP domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (24490_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxynitrite isomerase THAP4 in blood serum http://purl.obolibrary.org/obo/OBA_2044365 GCST90236653 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myotubularin-related protein 7 level in Chronic kidney disease with hypertension and no diabetes (24493_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of myotubularin-related protein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2042454 GCST90236654 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Katanin p60 ATPase-containing subunit A-like 1 level in Chronic kidney disease with hypertension and no diabetes (24494_67) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of katanin p60 ATPase-containing subunit A-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042083 GCST90236655 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RILP-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (24496_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RILP-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043274 GCST90236656 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable E3 ubiquitin-protein ligase TRIML1 level in Chronic kidney disease with hypertension and no diabetes (24497_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable E3 ubiquitin-protein ligase TRIML1 in blood serum http://purl.obolibrary.org/obo/OBA_2044590 GCST90236657 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lengsin level in Chronic kidney disease with hypertension and no diabetes (24499_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lengsin in blood serum http://purl.obolibrary.org/obo/OBA_2042191 GCST90236658 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-dependent phospholipase A2 level in Chronic kidney disease with hypertension and no diabetes (2449_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 calcium-dependent phospholipase A2 measurement http://www.ebi.ac.uk/efo/EFO_0020216 GCST90236659 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein ripply3 level in Chronic kidney disease with hypertension and no diabetes (24634_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein ripply3 in blood serum http://purl.obolibrary.org/obo/OBA_2041368 GCST90236660 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trafficking protein particle complex subunit 6A level in Chronic kidney disease with hypertension and no diabetes (24635_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trafficking protein particle complex subunit 6A in blood serum http://purl.obolibrary.org/obo/OBA_2043922 GCST90236661 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dr1-associated corepressor level in Chronic kidney disease with hypertension and no diabetes (24636_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Dr1-associated corepressor in blood serum http://purl.obolibrary.org/obo/OBA_2041362 GCST90236662 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein-like 5 level in Chronic kidney disease with hypertension and no diabetes (24637_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein-like 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043808 GCST90236663 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hairy/enhancer-of-split related with YRPW motif protein 1 level in Chronic kidney disease with hypertension and no diabetes (24640_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hairy/enhancer-of-split related with YRPW motif protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041868 GCST90236664 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Claudin-1 level in Chronic kidney disease with hypertension and no diabetes (24641_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of claudin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041042 GCST90236665 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM92A level in Chronic kidney disease with hypertension and no diabetes (24642_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CBY1-interacting BAR domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044740 GCST90236666 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dynamin-1 level in Chronic kidney disease with hypertension and no diabetes (24435_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dynamin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041334 GCST90236617 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disks large-associated protein 4 level in Chronic kidney disease with hypertension and no diabetes (24436_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disks large-associated protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041312 GCST90236618 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. YjeF N-terminal domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (24437_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of YjeF N-terminal domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044163 GCST90236619 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 8 isoform B level in Chronic kidney disease with hypertension and no diabetes (2443_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor 8 isoform b measurement http://www.ebi.ac.uk/efo/EFO_0020386 GCST90236620 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BTB/POZ domain-containing protein KCTD3 level in Chronic kidney disease with hypertension and no diabetes (24440_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of BTB/POZ domain-containing protein KCTD3 in blood serum http://purl.obolibrary.org/obo/OBA_2044318 GCST90236621 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear cap-binding protein subunit 1 level in Chronic kidney disease with hypertension and no diabetes (24441_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear cap-binding protein subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042523 GCST90236622 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mortality factor 4-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (24443_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mortality factor 4-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042402 GCST90236623 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 27 level in Chronic kidney disease with hypertension and no diabetes (24444_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tetratricopeptide repeat protein 27 in blood serum http://purl.obolibrary.org/obo/OBA_2044387 GCST90236624 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Actin filament-associated protein 1-like 2 level in Chronic kidney disease with hypertension and no diabetes (24445_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin filament-associated protein 1-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040531 GCST90236625 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Muscleblind-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (24446_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of muscleblind-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042310 GCST90236626 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM221A level in Chronic kidney disease with hypertension and no diabetes (24447_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM221A in blood serum http://purl.obolibrary.org/obo/OBA_2044733 GCST90236627 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-crystallin A level in Chronic kidney disease with hypertension and no diabetes (24449_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-crystallin A in blood serum http://purl.obolibrary.org/obo/OBA_2041158 GCST90236628 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0692 protein C19orf54 level in Chronic kidney disease with hypertension and no diabetes (24450_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UPF0692 protein C19orf54 in blood serum http://purl.obolibrary.org/obo/OBA_2044828 GCST90236629 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c-type heme lyase level in Chronic kidney disease with hypertension and no diabetes (24453_75) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of holocytochrome c-type synthase in blood serum http://purl.obolibrary.org/obo/OBA_2041844 GCST90236630 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2 level in Chronic kidney disease with hypertension and no diabetes (24454_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044496 GCST90236631 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (24455_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040690 GCST90236632 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Visual system homeobox 1 level in Chronic kidney disease with hypertension and no diabetes (24456_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of visual system homeobox 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044117 GCST90236633 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. USF2 level in Chronic kidney disease with hypertension and no diabetes (24457_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of upstream stimulatory factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044049 GCST90236634 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coatomer subunit beta' level in Chronic kidney disease with hypertension and no diabetes (24459_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coatomer subunit beta' in blood serum http://purl.obolibrary.org/obo/OBA_2041094 GCST90236635 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclic nucleotide-gated cation channel beta-1 level in Chronic kidney disease with hypertension and no diabetes (24462_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclic nucleotide-gated cation channel beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041065 GCST90236636 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein NDRG2 level in Chronic kidney disease with hypertension and no diabetes (24463_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein NDRG2 in blood serum http://purl.obolibrary.org/obo/OBA_2042536 GCST90236637 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. synovial sarcoma, X breakpoint 4 level in Chronic kidney disease with hypertension and no diabetes (24465_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein SSX4 in blood serum http://purl.obolibrary.org/obo/OBA_2043669 GCST90236638 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-adducin level in Chronic kidney disease with hypertension and no diabetes (24468_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-adducin in blood serum http://purl.obolibrary.org/obo/OBA_2040512 GCST90236639 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidate phosphatase LPIN1 level in Chronic kidney disease with hypertension and no diabetes (24469_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidate phosphatase LPIN1 in blood serum http://purl.obolibrary.org/obo/OBA_2042222 GCST90236640 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SET-binding protein level in Chronic kidney disease with hypertension and no diabetes (24471_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of SET-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2043468 GCST90236641 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanylate-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (18891_98) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of guanylate-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041681 GCST90235048 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glypican-4 level in Chronic kidney disease with hypertension and no diabetes (18892_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glypican-4 in blood serum http://purl.obolibrary.org/obo/OBA_2041769 GCST90235049 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adhesion G-protein coupled receptor G1 level in Chronic kidney disease with hypertension and no diabetes (18893_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of adhesion G-protein coupled receptor G1 in blood serum http://purl.obolibrary.org/obo/OBA_2041775 GCST90235050 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione peroxidase 2 level in Chronic kidney disease with hypertension and no diabetes (18894_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione peroxidase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041778 GCST90235051 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutathione S-transferase Mu 4 level in Chronic kidney disease with hypertension and no diabetes (18895_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutathione S-transferase mu 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044400 GCST90235052 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan-sulfate 6-O-sulfotransferase 3 level in Chronic kidney disease with hypertension and no diabetes (18896_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heparan-sulfate 6-O-sulfotransferase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041936 GCST90235053 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone deacetylase 2 level in Chronic kidney disease with hypertension and no diabetes (18897_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone deacetylase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041846 GCST90235054 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatoma-derived growth factor-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (18898_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of hepatoma-derived growth factor-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041850 GCST90235055 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatoma-derived growth factor-related protein 3 level in Chronic kidney disease with hypertension and no diabetes (18899_82) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of hepatoma-derived growth factor-related protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041851 GCST90235056 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTPase HRas level in Chronic kidney disease with hypertension and no diabetes (18900_37) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of GTPase HRas in blood serum http://purl.obolibrary.org/obo/OBA_2044350 GCST90235057 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock 70 kDa protein 1B level in Chronic kidney disease with hypertension and no diabetes (18901_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heat shock 70 kDa protein 1B in blood serum http://purl.obolibrary.org/obo/OBA_2044225 GCST90235058 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium/calmodulin-dependent protein kinase type IV level in Chronic kidney disease with hypertension and no diabetes (18904_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium/calmodulin-dependent protein kinase type IV in blood serum http://purl.obolibrary.org/obo/OBA_2040883 GCST90235059 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type I cytoskeletal 16 level in Chronic kidney disease with hypertension and no diabetes (18905_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type I cytoskeletal 16 in blood serum http://purl.obolibrary.org/obo/OBA_2042139 GCST90235060 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 3DL1 level in Chronic kidney disease with hypertension and no diabetes (18907_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of killer cell immunoglobulin-like receptor 3DL1 in blood serum http://purl.obolibrary.org/obo/OBA_2042109 GCST90235061 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Exosome complex component RRP43 level in Chronic kidney disease with hypertension and no diabetes (18909_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of exosome complex component RRP43 in blood serum http://purl.obolibrary.org/obo/OBA_2041528 GCST90235062 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein lin-7 homolog A level in Chronic kidney disease with hypertension and no diabetes (18910_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein lin-7 homolog A in blood serum http://purl.obolibrary.org/obo/OBA_2042205 GCST90235063 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-H level in Chronic kidney disease with hypertension and no diabetes (18913_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-H in blood serum http://purl.obolibrary.org/obo/OBA_2040935 GCST90235064 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet-activating factor acetylhydrolase 2, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (18914_188) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of platelet-activating factor acetylhydrolase 2, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2042746 GCST90235065 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inosine triphosphate pyrophosphatase level in Chronic kidney disease with hypertension and no diabetes (18916_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of inosine triphosphate pyrophosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2042060 GCST90235066 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pancreatic alpha-amylase level in Chronic kidney disease with hypertension and no diabetes (18917_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-amylase 2A in blood serum http://purl.obolibrary.org/obo/OBA_2040585 GCST90235067 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cAMP-specific 3',5'-cyclic phosphodiesterase 4A level in Chronic kidney disease with hypertension and no diabetes (18918_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cAMP-specific 3',5'-cyclic phosphodiesterase 4A in blood serum http://purl.obolibrary.org/obo/OBA_2042820 GCST90235068 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphate-regulating neutral endopeptidase level in Chronic kidney disease with hypertension and no diabetes (18921_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphate-regulating neutral endopeptidase PHEX in blood serum http://purl.obolibrary.org/obo/OBA_2044341 GCST90235069 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Macrosialin level in Chronic kidney disease with hypertension and no diabetes (18922_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of macrosialin in blood serum http://purl.obolibrary.org/obo/OBA_2040383 GCST90235070 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-5 level in Chronic kidney disease with hypertension and no diabetes (18925_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit alpha type-5 in blood serum http://purl.obolibrary.org/obo/OBA_2043065 GCST90235071 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit alpha type-3 level in Chronic kidney disease with hypertension and no diabetes (18926_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit alpha type-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043063 GCST90235072 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Retinoic acid early transcript 1G protein level in Chronic kidney disease with hypertension and no diabetes (18927_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UL-16 binding protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043184 GCST90235073 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-Z level in Chronic kidney disease with hypertension and no diabetes (18928_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-Z in blood serum http://purl.obolibrary.org/obo/OBA_2043372 GCST90235074 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Slit homolog 2 protein level in Chronic kidney disease with hypertension and no diabetes (18930_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of slit homolog 2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043545 GCST90235075 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Slit homolog 3 protein level in Chronic kidney disease with hypertension and no diabetes (18931_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of slit homolog 3 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043546 GCST90235076 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (18932_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nicotinamide/nicotinic acid mononucleotide adenylyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042599 GCST90235077 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-glutamine gamma-glutamyltransferase 4 level in Chronic kidney disease with hypertension and no diabetes (18933_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-glutamine gamma-glutamyltransferase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043840 GCST90235078 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-glutamine gamma-glutamyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (18934_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein-glutamine gamma-glutamyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043839 GCST90235079 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll-like receptor 5 level in Chronic kidney disease with hypertension and no diabetes (18935_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Toll-like receptor 5 in blood serum http://purl.obolibrary.org/obo/OBA_2040251 GCST90235080 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Very low-density lipoprotein receptor level in Chronic kidney disease with hypertension and no diabetes (18938_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of very low-density lipoprotein receptor in blood serum http://purl.obolibrary.org/obo/OBA_2044103 GCST90235081 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome subunit beta type-9 level in Chronic kidney disease with hypertension and no diabetes (18942_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proteasome subunit beta type-9 in blood serum http://purl.obolibrary.org/obo/OBA_2043073 GCST90235082 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostaglandin reductase 2 level in Chronic kidney disease with hypertension and no diabetes (18943_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostaglandin reductase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043093 GCST90235083 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Regulator of G-protein signaling 1 level in Chronic kidney disease with hypertension and no diabetes (18945_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of regulator of G-protein signaling 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043252 GCST90235084 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 3B level in Chronic kidney disease with hypertension and no diabetes (18947_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 3B in blood serum http://purl.obolibrary.org/obo/OBA_2044594 GCST90235085 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Methyl-CpG-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (19108_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methyl-CpG-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042324 GCST90235086 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein-like 8 level in Chronic kidney disease with hypertension and no diabetes (19109_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein-like 8 in blood serum http://purl.obolibrary.org/obo/OBA_2043810 GCST90235087 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein MEMO1 level in Chronic kidney disease with hypertension and no diabetes (19110_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein MEMO1 in blood serum http://purl.obolibrary.org/obo/OBA_2042335 GCST90235088 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NEDD8-conjugating enzyme Ubc12 level in Chronic kidney disease with hypertension and no diabetes (19111_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NEDD8-conjugating enzyme Ubc12 in blood serum http://purl.obolibrary.org/obo/OBA_2043999 GCST90235089 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein-like 3 level in Chronic kidney disease with hypertension and no diabetes (19112_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein-like 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043806 GCST90235090 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 domain-binding glutamic acid-rich-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (19113_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH3 domain-binding glutamic acid-rich-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044465 GCST90235091 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thymidine kinase 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19114_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thymidine kinase 2, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043862 GCST90235092 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxymethylenebutenolidase homolog level in Chronic kidney disease with hypertension and no diabetes (19115_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxymethylenebutenolidase in blood serum http://purl.obolibrary.org/obo/OBA_2041063 GCST90235093 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Biogenesis of lysosome-related organelles complex 1 subunit 5 level in Chronic kidney disease with hypertension and no diabetes (19116_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Muted in blood serum http://purl.obolibrary.org/obo/OBA_2042465 GCST90235094 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein phosphatase 1 regulatory subunit 14A level in Chronic kidney disease with hypertension and no diabetes (19117_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein phosphatase 1 regulatory subunit 14A in blood serum http://purl.obolibrary.org/obo/OBA_2043001 GCST90235095 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteoclast-stimulating factor 1 level in Chronic kidney disease with hypertension and no diabetes (19118_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of osteoclast-stimulating factor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042716 GCST90235096 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA damage-inducible transcript 3 protein level in Chronic kidney disease with hypertension and no diabetes (19119_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA damage-inducible transcript 3 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041254 GCST90235097 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lambda-crystallin homolog level in Chronic kidney disease with hypertension and no diabetes (24643_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lambda-crystallin in blood serum http://purl.obolibrary.org/obo/OBA_2041162 GCST90236667 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bridging integrator 3 level in Chronic kidney disease with hypertension and no diabetes (24645_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bridging integrator 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040800 GCST90236668 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine--pyruvate aminotransferase level in Chronic kidney disease with hypertension and no diabetes (24646_47) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alanine--glyoxylate aminotransferase in blood serum http://purl.obolibrary.org/obo/OBA_2044448 GCST90236669 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C->U-editing enzyme APOBEC-2 level in Chronic kidney disease with hypertension and no diabetes (24647_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C->U-editing enzyme APOBEC-2 in blood serum http://purl.obolibrary.org/obo/OBA_2044617 GCST90236670 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histone RNA hairpin-binding protein level in Chronic kidney disease with hypertension and no diabetes (24648_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histone RNA hairpin-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2043523 GCST90236671 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein N-terminal glutamine amidohydrolase level in Chronic kidney disease with hypertension and no diabetes (24649_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein N-terminal glutamine amidohydrolase in blood serum http://purl.obolibrary.org/obo/OBA_2044709 GCST90236672 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Reticulon-1 level in Chronic kidney disease with hypertension and no diabetes (24651_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of reticulon-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043352 GCST90236673 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription cofactor HES-6 level in Chronic kidney disease with hypertension and no diabetes (24654_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription cofactor HES-6 in blood serum http://purl.obolibrary.org/obo/OBA_2041863 GCST90236674 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RILP-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (24655_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RILP-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043275 GCST90236675 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sesquipedalian-2 level in Chronic kidney disease with hypertension and no diabetes (24656_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sesquipedalian-2 in blood serum http://purl.obolibrary.org/obo/OBA_2044761 GCST90236676 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 3DL2 level in Chronic kidney disease with hypertension and no diabetes (5096_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 killer cell immunoglobulin-like receptor 3DL2 measurement http://www.ebi.ac.uk/efo/EFO_0020518 GCST90237839 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell immunoglobulin-like receptor 3DS1 level in Chronic kidney disease with hypertension and no diabetes (5097_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 killer cell immunoglobulin-like receptor 3DS1 measurement http://www.ebi.ac.uk/efo/EFO_0020519 GCST90237840 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Killer cell lectin-like receptor subfamily F member 1 level in Chronic kidney disease with hypertension and no diabetes (5098_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 killer cell lectin-like receptor subfamily F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0020520 GCST90237841 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte activation gene 3 protein level in Chronic kidney disease with hypertension and no diabetes (5099_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphocyte activation gene 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0020540 GCST90237842 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysosome membrane protein 2 level in Chronic kidney disease with hypertension and no diabetes (5100_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 lysosome membrane protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0020545 GCST90237843 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MHC class I polypeptide-related sequence B level in Chronic kidney disease with hypertension and no diabetes (5102_55) 466 African American individuals NA Illumina [14870897] (imputed) 1 MHC class I polypeptide-related sequence B measurement http://www.ebi.ac.uk/efo/EFO_0008234 GCST90237844 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell surface glycoprotein CD200 receptor 1 level in Chronic kidney disease with hypertension and no diabetes (5103_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 cell surface glycoprotein CD200 receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020253 GCST90237845 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Natural cytotoxicity triggering receptor 1 level in Chronic kidney disease with hypertension and no diabetes (5104_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 natural cytotoxicity triggering receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020588 GCST90237846 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Reticulon-4 receptor level in Chronic kidney disease with hypertension and no diabetes (5105_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 reticulon-4 receptor measurement http://www.ebi.ac.uk/efo/EFO_0020705 GCST90237847 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurogenic locus notch homolog protein 1 level in Chronic kidney disease with hypertension and no diabetes (5107_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurogenic locus notch homolog protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0008246 GCST90237848 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurogenic locus notch homolog protein 3 level in Chronic kidney disease with hypertension and no diabetes (5108_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurogenic locus notch homolog protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0020600 GCST90237849 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuronal cell adhesion molecule level in Chronic kidney disease with hypertension and no diabetes (5109_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuronal cell adhesion molecule measurement http://www.ebi.ac.uk/efo/EFO_0020602 GCST90237850 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexin-1-beta level in Chronic kidney disease with hypertension and no diabetes (5110_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurexin-1-beta measurement http://www.ebi.ac.uk/efo/EFO_0020596 GCST90237851 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurexin-3-beta level in Chronic kidney disease with hypertension and no diabetes (5111_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 neurexin-3-beta measurement http://www.ebi.ac.uk/efo/EFO_0020597 GCST90237852 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. OX-2 membrane glycoprotein level in Chronic kidney disease with hypertension and no diabetes (5112_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 OX-2 membrane glycoprotein measurement http://www.ebi.ac.uk/efo/EFO_0008253 GCST90237853 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prolactin receptor level in Chronic kidney disease with hypertension and no diabetes (5114_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 prolactin receptor measurement http://www.ebi.ac.uk/efo/EFO_0020656 GCST90237854 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 19L level in Chronic kidney disease with hypertension and no diabetes (5115_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 19L measurement http://www.ebi.ac.uk/efo/EFO_0008309 GCST90237855 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Roundabout homolog 2 level in Chronic kidney disease with hypertension and no diabetes (5116_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 roundabout homolog 2 measurement http://www.ebi.ac.uk/efo/EFO_0020713 GCST90237856 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Roundabout homolog 3 level in Chronic kidney disease with hypertension and no diabetes (5117_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 roundabout homolog 3 measurement http://www.ebi.ac.uk/efo/EFO_0020714 GCST90237857 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-6B level in Chronic kidney disease with hypertension and no diabetes (5121_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 semaphorin-6B measurement http://www.ebi.ac.uk/efo/EFO_0021885 GCST90237858 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-6A level in Chronic kidney disease with hypertension and no diabetes (5122_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 semaphorin-6A measurement http://www.ebi.ac.uk/efo/EFO_0020721 GCST90237859 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 5 level in Chronic kidney disease with hypertension and no diabetes (5124_62) 466 African American individuals NA Illumina [14870897] (imputed) 1 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90237860 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 5 level in Chronic kidney disease with hypertension and no diabetes (5124_69) 466 African American individuals NA Illumina [14870897] (imputed) 1 intercellular adhesion molecule 5 measurement http://www.ebi.ac.uk/efo/EFO_0008164 GCST90237861 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLAM family member 6 level in Chronic kidney disease with hypertension and no diabetes (5128_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 SLAM family member 6 measurement http://www.ebi.ac.uk/efo/EFO_0020742 GCST90237862 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor class F member 1 level in Chronic kidney disease with hypertension and no diabetes (5129_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 scavenger receptor class F member 1 measurement http://www.ebi.ac.uk/efo/EFO_0008276 GCST90237863 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 19 level in Chronic kidney disease with hypertension and no diabetes (5131_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 19 measurement http://www.ebi.ac.uk/efo/EFO_0020808 GCST90237864 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-27 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (5132_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-27 receptor subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042014 GCST90237865 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TGF-beta receptor type-2 level in Chronic kidney disease with hypertension and no diabetes (5133_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 tgf-beta receptor type-2 measurement http://www.ebi.ac.uk/efo/EFO_0020767 GCST90237866 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hepatitis A virus cellular receptor 2 level in Chronic kidney disease with hypertension and no diabetes (5134_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 hepatitis A virus cellular receptor 2 measurement http://www.ebi.ac.uk/efo/EFO_0008151 GCST90237867 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5C level in Chronic kidney disease with hypertension and no diabetes (5139_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 netrin receptor UNC5C measurement http://www.ebi.ac.uk/efo/EFO_0020590 GCST90237868 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin receptor UNC5D level in Chronic kidney disease with hypertension and no diabetes (5140_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 netrin receptor UNC5D measurement http://www.ebi.ac.uk/efo/EFO_0020591 GCST90237869 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A level in Chronic kidney disease with hypertension and no diabetes (5178_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7a measurement http://www.ebi.ac.uk/efo/EFO_0020445 GCST90237870 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AMP Kinase (alpha1beta1gamma1) level in Chronic kidney disease with hypertension and no diabetes (5183_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 amp kinase (alpha1beta1gamma1) measurement http://www.ebi.ac.uk/efo/EFO_0020142 GCST90237871 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTPase KRas level in Chronic kidney disease with hypertension and no diabetes (5193_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 GTPase kras measurement http://www.ebi.ac.uk/efo/EFO_0020432 GCST90237872 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycylpeptide N-tetradecanoyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (5196_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 glycylpeptide n-tetradecanoyltransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020413 GCST90237873 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A level in Chronic kidney disease with hypertension and no diabetes (5201_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 high affinity cgmp-specific 3',5'-cyclic phosphodiesterase 9a measurement http://www.ebi.ac.uk/efo/EFO_0020446 GCST90237874 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Proteasome activator complex subunit 3 level in Chronic kidney disease with hypertension and no diabetes (5204_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 proteasome activator complex subunit 3 measurement http://www.ebi.ac.uk/efo/EFO_0020662 GCST90237875 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucokinase regulatory protein level in Chronic kidney disease with hypertension and no diabetes (5223_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 glucokinase regulatory protein measurement http://www.ebi.ac.uk/efo/EFO_0020406 GCST90237876 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase II 2-alpha:2-beta heterotetramer level in Chronic kidney disease with hypertension and no diabetes (5225_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 casein kinase II 2-alpha:2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020236 GCST90237877 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Casein kinase II 2-alpha':2-beta heterotetramer level in Chronic kidney disease with hypertension and no diabetes (5226_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 casein kinase II 2-alpha':2-beta heterotetramer measurement http://www.ebi.ac.uk/efo/EFO_0020237 GCST90237878 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein sorting-associated protein 26A level in Chronic kidney disease with hypertension and no diabetes (19293_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vacuolar protein sorting-associated protein 26A in blood serum http://purl.obolibrary.org/obo/OBA_2044108 GCST90235209 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich PDZ-binding protein level in Chronic kidney disease with hypertension and no diabetes (19294_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine-rich PDZ-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2041143 GCST90235210 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase PP1-gamma catalytic subunit level in Chronic kidney disease with hypertension and no diabetes (19295_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein phosphatase PP1-gamma catalytic subunit in blood serum http://purl.obolibrary.org/obo/OBA_2042999 GCST90235211 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin regulatory light chain 2, atrial isoform level in Chronic kidney disease with hypertension and no diabetes (19296_51) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of myosin regulatory light chain 2, atrial isoform in blood serum http://purl.obolibrary.org/obo/OBA_2042483 GCST90235212 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucose-6-phosphate 1-dehydrogenase level in Chronic kidney disease with hypertension and no diabetes (19297_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glucose-6-phosphate 1-dehydrogenase in blood serum http://purl.obolibrary.org/obo/OBA_2041645 GCST90235213 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTPase IMAP family member 6 level in Chronic kidney disease with hypertension and no diabetes (19302_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTPase IMAP family member 6 in blood serum http://purl.obolibrary.org/obo/OBA_2044751 GCST90235214 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein PET117 homolog, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19303_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein PET117 homolog, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044671 GCST90235215 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coatomer subunit epsilon level in Chronic kidney disease with hypertension and no diabetes (19310_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coatomer subunit epsilon in blood serum http://purl.obolibrary.org/obo/OBA_2041095 GCST90235216 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-crystallin S level in Chronic kidney disease with hypertension and no diabetes (19311_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gamma-crystallin S in blood serum http://purl.obolibrary.org/obo/OBA_2041161 GCST90235217 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Iron-sulfur cluster co-chaperone protein HscB, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (19316_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of iron-sulfur cluster co-chaperone protein HscB in blood serum http://purl.obolibrary.org/obo/OBA_2041937 GCST90235218 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostatic acid phosphatase level in Chronic kidney disease with hypertension and no diabetes (19317_114) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostatic acid phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2040485 GCST90235219 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Receptor-binding cancer antigen expressed on SiSo cells level in Chronic kidney disease with hypertension and no diabetes (19323_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of receptor-binding cancer antigen expressed on SiSo cells in blood serum http://purl.obolibrary.org/obo/OBA_2041404 GCST90235220 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein ABHD14B level in Chronic kidney disease with hypertension and no diabetes (19325_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative protein-lysine deacylase ABHD14B in blood serum http://purl.obolibrary.org/obo/OBA_2040459 GCST90235221 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase Chk2 level in Chronic kidney disease with hypertension and no diabetes (19328_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase CHK2 measurement http://www.ebi.ac.uk/efo/EFO_0020726 GCST90235222 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeodomain-interacting protein kinase 3 level in Chronic kidney disease with hypertension and no diabetes (19329_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 homeodomain-interacting protein kinase 3 measurement http://www.ebi.ac.uk/efo/EFO_0020457 GCST90235223 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Brain-specific angiogenesis inhibitor 1-associated protein 2 level in Chronic kidney disease with hypertension and no diabetes (19331_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of brain-specific angiogenesis inhibitor 1-associated protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040775 GCST90235224 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MOB-like protein phocein level in Chronic kidney disease with hypertension and no diabetes (19332_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MOB-like protein phocein in blood serum http://purl.obolibrary.org/obo/OBA_2042397 GCST90235225 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein K level in Chronic kidney disease with hypertension and no diabetes (19333_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 heterogeneous nuclear ribonucleoprotein k measurement http://www.ebi.ac.uk/efo/EFO_0020442 GCST90235226 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin domain-containing protein 12 level in Chronic kidney disease with hypertension and no diabetes (19334_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 thioredoxin domain-containing protein 12 measurement http://www.ebi.ac.uk/efo/EFO_0008298 GCST90235227 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hematological and neurological expressed 1 protein level in Chronic kidney disease with hypertension and no diabetes (19335_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of jupiter microtubule associated homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041898 GCST90235228 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein LZIC level in Chronic kidney disease with hypertension and no diabetes (19338_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein LZIC in blood serum http://purl.obolibrary.org/obo/OBA_2042254 GCST90235229 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-CoA-binding domain-containing protein 6 level in Chronic kidney disease with hypertension and no diabetes (19341_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-CoA-binding domain-containing protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040475 GCST90235230 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carbonic anhydrase 12 level in Chronic kidney disease with hypertension and no diabetes (19347_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carbonic anhydrase 12 in blood serum http://purl.obolibrary.org/obo/OBA_2040858 GCST90235231 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteopetrosis-associated transmembrane protein 1 level in Chronic kidney disease with hypertension and no diabetes (19353_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of osteopetrosis-associated transmembrane protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042717 GCST90235232 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 115 level in Chronic kidney disease with hypertension and no diabetes (24658_98) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 115 in blood serum http://purl.obolibrary.org/obo/OBA_2044703 GCST90236677 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 10B level in Chronic kidney disease with hypertension and no diabetes (5534_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 10B measurement http://www.ebi.ac.uk/efo/EFO_0021993 GCST90237966 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropilin-1 level in Chronic kidney disease with hypertension and no diabetes (5542_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 neuropilin-1 measurement http://www.ebi.ac.uk/efo/EFO_0020603 GCST90237967 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tyrosine-protein kinase RYK level in Chronic kidney disease with hypertension and no diabetes (5583_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tyrosine-protein kinase RYK in blood serum http://purl.obolibrary.org/obo/OBA_2043361 GCST90237968 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Holo-Transcobalamin-2 level in Chronic kidney disease with hypertension and no diabetes (5584_21) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of transcobalamin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043816 GCST90237969 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Multiple inositol polyphosphate phosphatase 1 level in Chronic kidney disease with hypertension and no diabetes (5586_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of multiple inositol polyphosphate phosphatase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042369 GCST90237970 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 134 level in Chronic kidney disease with hypertension and no diabetes (5587_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 134 in blood serum http://purl.obolibrary.org/obo/OBA_2044258 GCST90237971 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zona pellucida-like domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (5590_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zona pellucida-like domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044766 GCST90237972 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase A5 level in Chronic kidney disease with hypertension and no diabetes (5593_11) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein disulfide-isomerase A5 in blood serum http://purl.obolibrary.org/obo/OBA_2042829 GCST90237973 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LDLR chaperone MESD level in Chronic kidney disease with hypertension and no diabetes (5594_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mesoderm development candidate 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042342 GCST90237974 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD5 level in Chronic kidney disease with hypertension and no diabetes (5596_75) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90237975 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gremlin-2 level in Chronic kidney disease with hypertension and no diabetes (5598_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gremlin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041786 GCST90237976 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prenylcysteine oxidase-like level in Chronic kidney disease with hypertension and no diabetes (5599_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prenylcysteine oxidase-like in blood serum http://purl.obolibrary.org/obo/OBA_2042810 GCST90237977 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. N-acetylmuramoyl-L-alanine amidase level in Chronic kidney disease with hypertension and no diabetes (5601_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of N-acetylmuramoyl-L-alanine amidase in blood serum http://purl.obolibrary.org/obo/OBA_2042862 GCST90237978 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive ribonuclease-like protein 10 level in Chronic kidney disease with hypertension and no diabetes (5602_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribonuclease-like protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2043281 GCST90237979 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-N-acetylglucosaminyltransferase manic fringe level in Chronic kidney disease with hypertension and no diabetes (5605_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-N-acetylglucosaminyltransferase manic fringe in blood serum http://purl.obolibrary.org/obo/OBA_2042354 GCST90237980 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microfibrillar-associated protein 1 level in Chronic kidney disease with hypertension and no diabetes (5606_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microfibrillar-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042348 GCST90237981 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM19A5 level in Chronic kidney disease with hypertension and no diabetes (5609_92) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chemokine-like protein TAFA-5 in blood serum http://purl.obolibrary.org/obo/OBA_2044470 GCST90237982 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM171A1 level in Chronic kidney disease with hypertension and no diabetes (5610_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein FAM171A1 in blood serum http://purl.obolibrary.org/obo/OBA_2044439 GCST90237983 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 108B level in Chronic kidney disease with hypertension and no diabetes (5611_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 108B in blood serum http://purl.obolibrary.org/obo/OBA_2041270 GCST90237984 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Histidine triad nucleotide-binding protein 2, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (5612_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of histidine triad nucleotide-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041876 GCST90237985 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Linker for activation of T-cells family member 2 level in Chronic kidney disease with hypertension and no diabetes (5613_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of linker for activation of T-cells family member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042168 GCST90237986 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Corticoliberin level in Chronic kidney disease with hypertension and no diabetes (5614_44) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of corticoliberin in blood serum http://purl.obolibrary.org/obo/OBA_2041139 GCST90237987 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM172A level in Chronic kidney disease with hypertension and no diabetes (5615_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cotranscriptional regulator FAM172A in blood serum http://purl.obolibrary.org/obo/OBA_2044460 GCST90237988 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pro-FMRFamide-related neuropeptide FF level in Chronic kidney disease with hypertension and no diabetes (5617_41) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of FMRFamide-related neuropeptide FF in blood serum http://purl.obolibrary.org/obo/OBA_2042613 GCST90237989 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-glycine alpha-amidating monooxygenase level in Chronic kidney disease with hypertension and no diabetes (5620_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-glycine alpha-amidating monooxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2042754 GCST90237990 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 13 level in Chronic kidney disease with hypertension and no diabetes (24659_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily B member 13 in blood serum http://purl.obolibrary.org/obo/OBA_2041327 GCST90236678 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. MAP6 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (24661_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of MAP6 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042292 GCST90236679 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetratricopeptide repeat protein 36 level in Chronic kidney disease with hypertension and no diabetes (24662_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tetratricopeptide repeat protein 36 in blood serum http://purl.obolibrary.org/obo/OBA_2044402 GCST90236680 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UPF0510 protein INM02 level in Chronic kidney disease with hypertension and no diabetes (24664_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ER membrane protein complex subunit 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044551 GCST90236681 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein REM 1 level in Chronic kidney disease with hypertension and no diabetes (24665_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein REM 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043238 GCST90236682 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cancer/testis antigen family 45 member A1 level in Chronic kidney disease with hypertension and no diabetes (24667_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cancer/testis antigen family 45 member A1 in blood serum http://purl.obolibrary.org/obo/OBA_2041179 GCST90236683 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 5B level in Chronic kidney disease with hypertension and no diabetes (24669_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 5B in blood serum http://purl.obolibrary.org/obo/OBA_2044528 GCST90236684 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PIH1 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (24670_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PIH1 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044423 GCST90236685 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Apoptosis-associated speck-like protein containing a CARD level in Chronic kidney disease with hypertension and no diabetes (24671_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of apoptosis-associated speck-like protein containing a CARD in blood serum http://purl.obolibrary.org/obo/OBA_2043122 GCST90236686 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Egl nine homolog 2 level in Chronic kidney disease with hypertension and no diabetes (24674_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prolyl hydroxylase EGLN2 in blood serum http://purl.obolibrary.org/obo/OBA_2041429 GCST90236687 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated serine/threonine-protein kinase 4 level in Chronic kidney disease with hypertension and no diabetes (24675_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated serine/threonine-protein kinase 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042303 GCST90236688 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C21orf59 level in Chronic kidney disease with hypertension and no diabetes (24676_105) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cilia- and flagella-associated protein 298 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044899 GCST90236689 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein RER1 level in Chronic kidney disease with hypertension and no diabetes (24677_106) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein RER1 in blood serum http://purl.obolibrary.org/obo/OBA_2043241 GCST90236690 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell death regulator Aven level in Chronic kidney disease with hypertension and no diabetes (24678_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell death regulator Aven in blood serum http://purl.obolibrary.org/obo/OBA_2040740 GCST90236691 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor ETV7 level in Chronic kidney disease with hypertension and no diabetes (24679_35) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of transcription factor ETV7 in blood serum http://purl.obolibrary.org/obo/OBA_2041519 GCST90236692 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thioredoxin domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (24680_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thioredoxin-related transmembrane protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043966 GCST90236693 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphoserine phosphatase level in Chronic kidney disease with hypertension and no diabetes (24681_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoserine phosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2043084 GCST90236694 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTPase IMAP family member 7 level in Chronic kidney disease with hypertension and no diabetes (24683_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTPase IMAP family member 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044690 GCST90236695 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTPase IMAP family member 4 level in Chronic kidney disease with hypertension and no diabetes (24684_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTPase IMAP family member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041718 GCST90236696 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-11 level in Chronic kidney disease with hypertension and no diabetes (24685_12) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of sorting nexin-11 in blood serum http://purl.obolibrary.org/obo/OBA_2043583 GCST90236697 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acyl-CoA-binding domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (24686_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acyl-CoA-binding domain-containing protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044582 GCST90236698 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-tocopherol transfer protein-like level in Chronic kidney disease with hypertension and no diabetes (24687_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-tocopherol transfer protein-like in blood serum http://purl.obolibrary.org/obo/OBA_2043959 GCST90236699 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Doublesex- and mab-3-related transcription factor B1 level in Chronic kidney disease with hypertension and no diabetes (24688_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of doublesex- and mab-3-related transcription factor B1 in blood serum http://purl.obolibrary.org/obo/OBA_2041323 GCST90236700 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polymerase I and transcript release factor level in Chronic kidney disease with hypertension and no diabetes (24689_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of caveolae-associated protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043111 GCST90236701 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 20 level in Chronic kidney disease with hypertension and no diabetes (2468_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 20 measurement http://www.ebi.ac.uk/efo/EFO_0010910 GCST90236702 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (24690_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040865 GCST90236703 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chloride intracellular channel protein 3 level in Chronic kidney disease with hypertension and no diabetes (24693_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chloride intracellular channel protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041049 GCST90236704 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ezrin-radixin-moesin-binding phosphoprotein 50 level in Chronic kidney disease with hypertension and no diabetes (24694_158) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Na(+)/H(+) exchange regulatory cofactor NHE-RF1 in blood serum http://purl.obolibrary.org/obo/OBA_2040235 GCST90236705 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pleckstrin homology domain-containing family B member 1 level in Chronic kidney disease with hypertension and no diabetes (24695_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pleckstrin homology domain-containing family B member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044628 GCST90236706 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ domain-containing protein MAGIX level in Chronic kidney disease with hypertension and no diabetes (24696_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ domain-containing protein MAGIX in blood serum http://purl.obolibrary.org/obo/OBA_2044385 GCST90236707 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ADP-ribosylation factor-like protein 6-interacting protein 1 level in Chronic kidney disease with hypertension and no diabetes (24699_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ADP-ribosylation factor-like protein 6-interacting protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040673 GCST90236708 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dystrobrevin alpha level in Chronic kidney disease with hypertension and no diabetes (24701_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dystrobrevin alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041373 GCST90236709 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 149 level in Chronic kidney disease with hypertension and no diabetes (24702_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 149 in blood serum http://purl.obolibrary.org/obo/OBA_2044549 GCST90236710 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COMM domain-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (24704_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of COMM domain-containing protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2044434 GCST90236711 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Craniofacial development protein 1 level in Chronic kidney disease with hypertension and no diabetes (24706_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of craniofacial development protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040993 GCST90236712 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein CXorf38 level in Chronic kidney disease with hypertension and no diabetes (24707_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uncharacterized protein CXorf38 in blood serum http://purl.obolibrary.org/obo/OBA_2044849 GCST90236713 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Short-chain dehydrogenase/reductase 3 level in Chronic kidney disease with hypertension and no diabetes (24708_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of short-chain dehydrogenase/reductase 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041295 GCST90236714 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Microtubule-associated tumor suppressor candidate 2 level in Chronic kidney disease with hypertension and no diabetes (24710_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of microtubule-associated tumor suppressor candidate 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044397 GCST90236715 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Short stature homeobox protein level in Chronic kidney disease with hypertension and no diabetes (24711_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of short stature homeobox protein in blood serum http://purl.obolibrary.org/obo/OBA_2043505 GCST90236716 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GTP-binding protein 10 level in Chronic kidney disease with hypertension and no diabetes (24712_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041818 GCST90236717 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PDZ domain-containing protein MAGIX level in Chronic kidney disease with hypertension and no diabetes (24713_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of PDZ domain-containing protein MAGIX in blood serum http://purl.obolibrary.org/obo/OBA_2044385 GCST90236718 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein phosphatase 2A regulatory subunit B' level in Chronic kidney disease with hypertension and no diabetes (24717_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein phosphatase 2A regulatory subunit B' in blood serum http://purl.obolibrary.org/obo/OBA_2043009 GCST90236719 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 75A level in Chronic kidney disease with hypertension and no diabetes (24718_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 75A in blood serum http://purl.obolibrary.org/obo/OBA_2044696 GCST90236720 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ankyrin repeat domain-containing protein 16 level in Chronic kidney disease with hypertension and no diabetes (24720_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ankyrin repeat domain-containing protein 16 in blood serum http://purl.obolibrary.org/obo/OBA_2044700 GCST90236721 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Golgi phosphoprotein 3 level in Chronic kidney disease with hypertension and no diabetes (24721_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Golgi phosphoprotein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041763 GCST90236722 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spindlin-3 level in Chronic kidney disease with hypertension and no diabetes (24722_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of spindlin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043628 GCST90236723 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 2 subunit 2 level in Chronic kidney disease with hypertension and no diabetes (24723_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 2 subunit 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041445 GCST90236724 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein sorting-associated protein 26B level in Chronic kidney disease with hypertension and no diabetes (24724_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vacuolar protein sorting-associated protein 26B in blood serum http://purl.obolibrary.org/obo/OBA_2044109 GCST90236725 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. COP9 signalosome complex subunit 5 level in Chronic kidney disease with hypertension and no diabetes (24725_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of COP9 signalosome complex subunit 5 in blood serum http://purl.obolibrary.org/obo/OBA_2041097 GCST90236726 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serum amyloid P-component level in Chronic kidney disease with hypertension and no diabetes (2474_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 serum amyloid P-component measurement http://www.ebi.ac.uk/efo/EFO_0008283 GCST90236727 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poly(U)-specific endoribonuclease level in Chronic kidney disease with hypertension and no diabetes (5656_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of uridylate-specific endoribonuclease in blood serum http://purl.obolibrary.org/obo/OBA_2044412 GCST90238016 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (5657_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMP-N-acetylneuraminate-beta-galactosamide-alpha-2,3-sialyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044500 GCST90238017 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coagulation factor XIII B chain level in Chronic kidney disease with hypertension and no diabetes (5658_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coagulation factor XIII B chain in blood serum http://purl.obolibrary.org/obo/OBA_2041534 GCST90238018 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pro-Thyrotropin-releasing hormone level in Chronic kidney disease with hypertension and no diabetes (5659_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pro-thyrotropin-releasing hormone in blood serum http://purl.obolibrary.org/obo/OBA_2043930 GCST90238019 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Extracellular superoxide dismutase [Cu-Zn] level in Chronic kidney disease with hypertension and no diabetes (5660_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of extracellular superoxide dismutase [Cu-Zn] in blood serum http://purl.obolibrary.org/obo/OBA_2043596 GCST90238020 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Platelet factor 4 variant level in Chronic kidney disease with hypertension and no diabetes (5663_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of platelet factor 4 variant in blood serum http://purl.obolibrary.org/obo/OBA_2042847 GCST90238021 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 106 level in Chronic kidney disease with hypertension and no diabetes (5664_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 106 in blood serum http://purl.obolibrary.org/obo/OBA_2041268 GCST90238022 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-1 receptor type 2 level in Chronic kidney disease with hypertension and no diabetes (5666_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-1 receptor type 2 measurement http://www.ebi.ac.uk/efo/EFO_0021842 GCST90238023 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-3B level in Chronic kidney disease with hypertension and no diabetes (5667_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-3B in blood serum http://purl.obolibrary.org/obo/OBA_2043427 GCST90238024 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Anterior gradient protein 3 level in Chronic kidney disease with hypertension and no diabetes (5668_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of anterior gradient protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2040537 GCST90238025 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal-regulatory protein beta-2 level in Chronic kidney disease with hypertension and no diabetes (5669_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal-regulatory protein beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043511 GCST90238026 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymotrypsinogen B level in Chronic kidney disease with hypertension and no diabetes (5671_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chymotrypsinogen B in blood serum http://purl.obolibrary.org/obo/OBA_2041191 GCST90238027 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin level in Chronic kidney disease with hypertension and no diabetes (5675_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90238028 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Agouti-signaling protein level in Chronic kidney disease with hypertension and no diabetes (5676_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of agouti-signaling protein in blood serum http://purl.obolibrary.org/obo/OBA_2040700 GCST90238029 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized protein C2orf66 level in Chronic kidney disease with hypertension and no diabetes (5677_15) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of uncharacterized protein C2orf66 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044907 GCST90238030 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 103 level in Chronic kidney disease with hypertension and no diabetes (5679_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 103 in blood serum http://purl.obolibrary.org/obo/OBA_2041266 GCST90238031 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Odorant-binding protein 2b level in Chronic kidney disease with hypertension and no diabetes (5680_54) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of odorant-binding protein 2b in blood serum http://purl.obolibrary.org/obo/OBA_2042689 GCST90238032 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 2 level in Chronic kidney disease with hypertension and no diabetes (12801_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon regulatory factor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040374 GCST90233700 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 329 level in Chronic kidney disease with hypertension and no diabetes (12803_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 329 in blood serum http://purl.obolibrary.org/obo/OBA_2044200 GCST90233701 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 30 level in Chronic kidney disease with hypertension and no diabetes (12807_89) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 30 in blood serum http://purl.obolibrary.org/obo/OBA_2040653 GCST90233702 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-regulated heat-stable protein 1 level in Chronic kidney disease with hypertension and no diabetes (12808_103) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-regulated heat-stable protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040900 GCST90233703 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 415 level in Chronic kidney disease with hypertension and no diabetes (12811_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 415 in blood serum http://purl.obolibrary.org/obo/OBA_2044206 GCST90233704 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acylphosphatase-2 level in Chronic kidney disease with hypertension and no diabetes (12812_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acylphosphatase-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040494 GCST90233705 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EH domain-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (12813_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of EH domain-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041431 GCST90233706 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RNA-binding protein 40 level in Chronic kidney disease with hypertension and no diabetes (12814_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding region-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043302 GCST90233707 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mast/stem cell growth factor receptor Kit level in Chronic kidney disease with hypertension and no diabetes (2475_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 mast/stem cell growth factor receptor kit measurement http://www.ebi.ac.uk/efo/EFO_0020554 GCST90236728 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Metalloproteinase inhibitor 3 level in Chronic kidney disease with hypertension and no diabetes (2480_58) 466 African American individuals NA Illumina [14870897] (imputed) 1 metalloproteinase inhibitor 3 measurement http://www.ebi.ac.uk/efo/EFO_0008231 GCST90236729 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor receptor kinase substrate 8-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (24891_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epidermal growth factor receptor kinase substrate 8-like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041498 GCST90236730 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testicular spindle-associated protein SHCBP1L level in Chronic kidney disease with hypertension and no diabetes (24892_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of testicular spindle-associated protein SHCBP1L in blood serum http://purl.obolibrary.org/obo/OBA_2044568 GCST90236731 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. F-BAR and double SH3 domains protein 1 level in Chronic kidney disease with hypertension and no diabetes (24895_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of F-BAR and double SH3 domains protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044461 GCST90236732 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Menin level in Chronic kidney disease with hypertension and no diabetes (24896_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of menin in blood serum http://purl.obolibrary.org/obo/OBA_2042336 GCST90236733 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sec1 family domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (24898_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Sec1 family domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043394 GCST90236734 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor receptor kinase substrate 8-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (24899_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epidermal growth factor receptor kinase substrate 8-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041497 GCST90236735 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Villin-1 level in Chronic kidney disease with hypertension and no diabetes (24901_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of villin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2044099 GCST90236736 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gephyrin level in Chronic kidney disease with hypertension and no diabetes (24902_84) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gephyrin in blood serum http://purl.obolibrary.org/obo/OBA_2041772 GCST90236737 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kelch-like protein 14 level in Chronic kidney disease with hypertension and no diabetes (24903_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kelch-like protein 14 in blood serum http://purl.obolibrary.org/obo/OBA_2042122 GCST90236738 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Syntaxin-binding protein 4 level in Chronic kidney disease with hypertension and no diabetes (24904_121) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of syntaxin-binding protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043719 GCST90236739 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein CXorf40A level in Chronic kidney disease with hypertension and no diabetes (24905_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein EOLA1 (human) in blood serum http://purl.obolibrary.org/obo/OBA_2044914 GCST90236740 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial-processing peptidase subunit alpha level in Chronic kidney disease with hypertension and no diabetes (24907_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of mitochondrial-processing peptidase subunit alpha in blood serum http://purl.obolibrary.org/obo/OBA_2042944 GCST90236741 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amphiphysin level in Chronic kidney disease with hypertension and no diabetes (24908_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of amphiphysin in blood serum http://purl.obolibrary.org/obo/OBA_2040583 GCST90236742 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 1-phosphatidylinositol-4,5-bisphosphate phosphodiesterase delta-1 level in Chronic kidney disease with hypertension and no diabetes (24909_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042919 GCST90236743 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Non-POU domain-containing octamer-binding protein level in Chronic kidney disease with hypertension and no diabetes (24910_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of non-POU domain-containing octamer-binding protein in blood serum http://purl.obolibrary.org/obo/OBA_2042605 GCST90236744 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LRP level in Chronic kidney disease with hypertension and no diabetes (24911_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of major vault protein in blood serum http://purl.obolibrary.org/obo/OBA_2042468 GCST90236745 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WD repeat-containing protein 26 level in Chronic kidney disease with hypertension and no diabetes (24912_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WD repeat-containing protein 26 in blood serum http://purl.obolibrary.org/obo/OBA_2044126 GCST90236746 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Enhancer of zeste homolog 2 level in Chronic kidney disease with hypertension and no diabetes (24914_10) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of histone-lysine N-methyltransferase EZH2 in blood serum http://purl.obolibrary.org/obo/OBA_2041531 GCST90236747 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calpain-13 level in Chronic kidney disease with hypertension and no diabetes (24915_123) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of calpain-13 in blood serum http://purl.obolibrary.org/obo/OBA_2040888 GCST90236748 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 1 level in Chronic kidney disease with hypertension and no diabetes (24917_95) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041330 GCST90236749 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaminase kidney isoform, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (24920_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutaminase kidney isoform, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041736 GCST90236750 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. HIRA-interacting protein 3 level in Chronic kidney disease with hypertension and no diabetes (24921_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of HIRA-interacting protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041878 GCST90236751 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NHL repeat-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (24922_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NHL repeat-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044334 GCST90236752 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombospondin type-1 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (5621_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of thrombospondin type-1 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044484 GCST90237991 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 1 level in Chronic kidney disease with hypertension and no diabetes (5623_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CMRF35-like molecule 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040943 GCST90237992 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Folate receptor gamma level in Chronic kidney disease with hypertension and no diabetes (5624_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of folate receptor gamma in blood serum http://purl.obolibrary.org/obo/OBA_2041603 GCST90237993 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymotrypsin-C level in Chronic kidney disease with hypertension and no diabetes (5626_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chymotrypsin-C in blood serum http://purl.obolibrary.org/obo/OBA_2041193 GCST90237994 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Progonadoliberin-1 level in Chronic kidney disease with hypertension and no diabetes (5627_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of progonadoliberin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041759 GCST90237995 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-3G level in Chronic kidney disease with hypertension and no diabetes (5628_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-3G in blood serum http://purl.obolibrary.org/obo/OBA_2043429 GCST90237996 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NKG2-A/NKG2-B type II integral membrane protein level in Chronic kidney disease with hypertension and no diabetes (5629_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NKG2-A/NKG2-B type II integral membrane protein in blood serum http://purl.obolibrary.org/obo/OBA_2040366 GCST90237997 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 8 level in Chronic kidney disease with hypertension and no diabetes (5630_48) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of CMRF35-like molecule 8 in blood serum http://purl.obolibrary.org/obo/OBA_2040299 GCST90237998 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Promotilin level in Chronic kidney disease with hypertension and no diabetes (5631_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of promotilin in blood serum http://purl.obolibrary.org/obo/OBA_2042380 GCST90237999 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cartilage acidic protein 1 level in Chronic kidney disease with hypertension and no diabetes (5632_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cartilage acidic protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041152 GCST90238000 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte immunoglobulin-like receptor subfamily B member 2 level in Chronic kidney disease with hypertension and no diabetes (5633_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 leukocyte immunoglobulin-like receptor subfamily B member 2 measurement http://www.ebi.ac.uk/efo/EFO_0008209 GCST90238001 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDP-fucose protein O-fucosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (5634_39) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of GDP-fucose protein O-fucosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042958 GCST90238002 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Triggering receptor expressed on myeloid cells 2 level in Chronic kidney disease with hypertension and no diabetes (5635_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of triggering receptor expressed on myeloid cells 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043927 GCST90238003 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Netrin-G1 level in Chronic kidney disease with hypertension and no diabetes (5637_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of netrin-G1 in blood serum http://purl.obolibrary.org/obo/OBA_2042655 GCST90238004 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Procollagen galactosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (5638_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of procollagen galactosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044308 GCST90238005 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuropilin and tolloid-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (5639_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuropilin and tolloid-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042562 GCST90238006 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epididymal-specific lipocalin-8 level in Chronic kidney disease with hypertension and no diabetes (5643_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epididymal-specific lipocalin-8 in blood serum http://purl.obolibrary.org/obo/OBA_2042174 GCST90238007 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease 4 level in Chronic kidney disease with hypertension and no diabetes (5644_60) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ribonuclease 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043284 GCST90238008 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribonuclease K6 level in Chronic kidney disease with hypertension and no diabetes (5646_20) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of ribonuclease K6 in blood serum http://purl.obolibrary.org/obo/OBA_2043285 GCST90238009 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chymotrypsinogen B2 level in Chronic kidney disease with hypertension and no diabetes (5648_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of chymotrypsinogen B2 in blood serum http://purl.obolibrary.org/obo/OBA_2041192 GCST90238010 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pregnancy-specific beta-1-glycoprotein 4 level in Chronic kidney disease with hypertension and no diabetes (5649_83) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of pregnancy-specific beta-1-glycoprotein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2043059 GCST90238011 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase A6 level in Chronic kidney disease with hypertension and no diabetes (5650_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein disulfide-isomerase A6 in blood serum http://purl.obolibrary.org/obo/OBA_2042830 GCST90238012 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative pregnancy-specific beta-1-glycoprotein 7 level in Chronic kidney disease with hypertension and no diabetes (5651_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pregnancy-specific beta-1-glycoprotein 7 in blood serum http://purl.obolibrary.org/obo/OBA_2044807 GCST90238013 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Probable inactive serine protease 37 level in Chronic kidney disease with hypertension and no diabetes (5653_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable inactive serine protease 37 in blood serum http://purl.obolibrary.org/obo/OBA_2044741 GCST90238014 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein disulfide-isomerase TMX3 level in Chronic kidney disease with hypertension and no diabetes (5654_70) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein disulfide-isomerase TXNDC10 in blood serum http://purl.obolibrary.org/obo/OBA_2043967 GCST90238015 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secernin-3 level in Chronic kidney disease with hypertension and no diabetes (24923_27) 466 African American individuals NA Illumina [14870897] (imputed) 2 level of secernin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043409 GCST90236753 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Far upstream element-binding protein 2 level in Chronic kidney disease with hypertension and no diabetes (24926_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of far upstream element-binding protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042095 GCST90236754 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitotic-spindle organizing protein 2A level in Chronic kidney disease with hypertension and no diabetes (24928_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitotic-spindle organizing protein 2A in blood serum http://purl.obolibrary.org/obo/OBA_2044694 GCST90236755 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor SOX-6 level in Chronic kidney disease with hypertension and no diabetes (24929_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor SOX-6 in blood serum http://purl.obolibrary.org/obo/OBA_2043603 GCST90236756 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor receptor kinase substrate 8-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (24931_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of epidermal growth factor receptor kinase substrate 8-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041499 GCST90236757 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Opioid growth factor receptor level in Chronic kidney disease with hypertension and no diabetes (24934_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of opioid growth factor receptor in blood serum http://purl.obolibrary.org/obo/OBA_2042695 GCST90236758 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Forkhead box protein P1 level in Chronic kidney disease with hypertension and no diabetes (24935_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of forkhead box protein P1 in blood serum http://purl.obolibrary.org/obo/OBA_2041613 GCST90236759 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 26 level in Chronic kidney disease with hypertension and no diabetes (24937_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 26 in blood serum http://purl.obolibrary.org/obo/OBA_2040652 GCST90236760 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AP-2 complex subunit beta-1 level in Chronic kidney disease with hypertension and no diabetes (24938_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AP-2 complex subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040612 GCST90236761 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inhibitor of nuclear factor kappa B kinase beta subunit level in Chronic kidney disease with hypertension and no diabetes (24940_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inhibitor of nuclear factor kappa-B kinase subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2040324 GCST90236762 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Clustered mitochondria protein homolog level in Chronic kidney disease with hypertension and no diabetes (24941_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of clustered mitochondria protein homolog in blood serum http://purl.obolibrary.org/obo/OBA_2044820 GCST90236763 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein unc-13 homolog D level in Chronic kidney disease with hypertension and no diabetes (24942_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein unc-13 homolog D in blood serum http://purl.obolibrary.org/obo/OBA_2044035 GCST90236764 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RalBP1-associated Eps domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (24944_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RalBP1-associated Eps domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043240 GCST90236765 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sorting nexin-27 level in Chronic kidney disease with hypertension and no diabetes (24945_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sorting nexin-27 in blood serum http://purl.obolibrary.org/obo/OBA_2043588 GCST90236766 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 22 level in Chronic kidney disease with hypertension and no diabetes (24946_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GTPase-activating protein 22 in blood serum http://purl.obolibrary.org/obo/OBA_2040649 GCST90236767 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Numb-like protein level in Chronic kidney disease with hypertension and no diabetes (24947_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Numb-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2042676 GCST90236768 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Paraspeckle component 1 level in Chronic kidney disease with hypertension and no diabetes (24948_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of paraspeckle component 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043083 GCST90236769 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Specifically androgen-regulated gene protein level in Chronic kidney disease with hypertension and no diabetes (24950_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of specifically androgen-regulated gene protein in blood serum http://purl.obolibrary.org/obo/OBA_2043382 GCST90236770 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein VAC14 homolog level in Chronic kidney disease with hypertension and no diabetes (24951_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein VAC14 in blood serum http://purl.obolibrary.org/obo/OBA_2044074 GCST90236771 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Far upstream element-binding protein 3 level in Chronic kidney disease with hypertension and no diabetes (24952_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of far upstream element-binding protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041630 GCST90236772 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Troponin I, cardiac muscle level in Chronic kidney disease with hypertension and no diabetes (5441_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 troponin i, cardiac muscle measurement http://www.ebi.ac.uk/efo/EFO_0020788 GCST90237936 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Atrial natriuretic factor level in Chronic kidney disease with hypertension and no diabetes (5443_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 atrial natriuretic factor measurement http://www.ebi.ac.uk/efo/EFO_0004789 GCST90237937 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD166 antigen level in Chronic kidney disease with hypertension and no diabetes (5451_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD166 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020245 GCST90237938 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Asialoglycoprotein receptor 1 level in Chronic kidney disease with hypertension and no diabetes (5452_71) 466 African American individuals NA Illumina [14870897] (imputed) 0 asialoglycoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020164 GCST90237939 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-Ala-His dipeptidase level in Chronic kidney disease with hypertension and no diabetes (5456_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 beta-Ala-His dipeptidase measurement http://www.ebi.ac.uk/efo/EFO_0008033 GCST90237940 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collectin-12 level in Chronic kidney disease with hypertension and no diabetes (5457_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90237941 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent RNA helicase DDX19B level in Chronic kidney disease with hypertension and no diabetes (5460_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 ATP-dependent rna helicase ddx19b measurement http://www.ebi.ac.uk/efo/EFO_0020167 GCST90237942 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ficolin-3 level in Chronic kidney disease with hypertension and no diabetes (5462_62) 466 African American individuals NA Illumina [14870897] (imputed) 1 ficolin-3 measurement http://www.ebi.ac.uk/efo/EFO_0020392 GCST90237943 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth arrest-specific protein 1 level in Chronic kidney disease with hypertension and no diabetes (5463_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 growth arrest-specific protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020425 GCST90237944 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Growth factor receptor-bound protein 2 level in Chronic kidney disease with hypertension and no diabetes (5464_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 growth factor receptor-bound protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021990 GCST90237945 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heparan-sulfate 6-O-sulfotransferase 1 level in Chronic kidney disease with hypertension and no diabetes (5465_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 heparan-sulfate 6-o-sulfotransferase 1 measurement http://www.ebi.ac.uk/efo/EFO_0020437 GCST90237946 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heat shock protein HSP 90-beta level in Chronic kidney disease with hypertension and no diabetes (5467_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 heat shock protein HSP 90-beta measurement http://www.ebi.ac.uk/efo/EFO_0021991 GCST90237947 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-17 receptor C level in Chronic kidney disease with hypertension and no diabetes (5468_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-17 receptor c measurement http://www.ebi.ac.uk/efo/EFO_0020494 GCST90237948 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C beta type (splice variant beta-II) level in Chronic kidney disease with hypertension and no diabetes (5475_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein kinase c beta type (splice variant beta-II) measurement http://www.ebi.ac.uk/efo/EFO_0020678 GCST90237949 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kinase C gamma type level in Chronic kidney disease with hypertension and no diabetes (5476_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein kinase c gamma type measurement http://www.ebi.ac.uk/efo/EFO_0020680 GCST90237950 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutamate carboxypeptidase 2 level in Chronic kidney disease with hypertension and no diabetes (5478_50) 466 African American individuals NA Illumina [14870897] (imputed) 0 glutamate carboxypeptidase 2 measurement http://www.ebi.ac.uk/efo/EFO_0020408 GCST90237951 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 5 level in Chronic kidney disease with hypertension and no diabetes (5480_49) 466 African American individuals NA Illumina [14870897] (imputed) 2 C-C motif chemokine 5 measurement http://www.ebi.ac.uk/efo/EFO_0008053 GCST90237952 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras GTPase-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (5481_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 ras GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020698 GCST90237953 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Repulsive guidance molecule A level in Chronic kidney disease with hypertension and no diabetes (5483_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 repulsive guidance molecule A measurement http://www.ebi.ac.uk/efo/EFO_0008273 GCST90237954 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S3a level in Chronic kidney disease with hypertension and no diabetes (5484_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 40S ribosomal protein S3a in blood serum http://purl.obolibrary.org/obo/OBA_2043335 GCST90237955 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Intercellular adhesion molecule 2 level in Chronic kidney disease with hypertension and no diabetes (5486_73) 466 African American individuals NA Illumina [14870897] (imputed) 0 intercellular adhesion molecule 2 measurement http://www.ebi.ac.uk/efo/EFO_0008163 GCST90237956 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLAM family member 7 level in Chronic kidney disease with hypertension and no diabetes (5487_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 SLAM family member 7 measurement http://www.ebi.ac.uk/efo/EFO_0008287 GCST90237957 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testican-1 level in Chronic kidney disease with hypertension and no diabetes (5490_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 testican-1 measurement http://www.ebi.ac.uk/efo/EFO_0020765 GCST90237958 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testican-2 level in Chronic kidney disease with hypertension and no diabetes (5491_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 testican-2 measurement http://www.ebi.ac.uk/efo/EFO_0020766 GCST90237959 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase WNK3 level in Chronic kidney disease with hypertension and no diabetes (5493_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 serine/threonine-protein kinase WNK3 measurement http://www.ebi.ac.uk/efo/EFO_0021992 GCST90237960 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Small nuclear ribonucleoprotein F level in Chronic kidney disease with hypertension and no diabetes (5494_52) 466 African American individuals NA Illumina [14870897] (imputed) 1 small nuclear ribonucleoprotein F measurement http://www.ebi.ac.uk/efo/EFO_0008288 GCST90237961 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Spondin-1 level in Chronic kidney disease with hypertension and no diabetes (5496_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 spondin-1 measurement http://www.ebi.ac.uk/efo/EFO_0008290 GCST90237962 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Epidermal growth factor level in Chronic kidney disease with hypertension and no diabetes (5509_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 epidermal growth factor measurement http://www.ebi.ac.uk/efo/EFO_0010947 GCST90237963 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor receptor superfamily member 18 level in Chronic kidney disease with hypertension and no diabetes (5526_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor receptor superfamily member 18 measurement http://www.ebi.ac.uk/efo/EFO_0020807 GCST90237964 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor receptor 1 level in Chronic kidney disease with hypertension and no diabetes (5532_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 fibroblast growth factor receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020388 GCST90237965 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADP-dependent malic enzyme level in Chronic kidney disease with hypertension and no diabetes (25060_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADP-dependent malic enzyme in blood serum http://purl.obolibrary.org/obo/OBA_2042322 GCST90236814 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Engulfment and cell motility protein 2 level in Chronic kidney disease with hypertension and no diabetes (25061_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of engulfment and cell motility protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041473 GCST90236815 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Type I inositol-3,4-bisphosphate 4-phosphatase level in Chronic kidney disease with hypertension and no diabetes (25064_34) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inositol polyphosphate-4-phosphatase type I A in blood serum http://purl.obolibrary.org/obo/OBA_2042029 GCST90236816 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin-binding protein H level in Chronic kidney disease with hypertension and no diabetes (25065_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin-binding protein H in blood serum http://purl.obolibrary.org/obo/OBA_2042476 GCST90236817 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glycogenin-2 level in Chronic kidney disease with hypertension and no diabetes (25066_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glycogenin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041825 GCST90236818 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein-methionine sulfoxide oxidase MICAL1 level in Chronic kidney disease with hypertension and no diabetes (25070_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of [F-actin]-monooxygenase MICAL1 in blood serum http://purl.obolibrary.org/obo/OBA_2042365 GCST90236819 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chromodomain-helicase-DNA-binding protein 1-like level in Chronic kidney disease with hypertension and no diabetes (25072_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chromodomain-helicase-DNA-binding protein 1-like in blood serum http://purl.obolibrary.org/obo/OBA_2041001 GCST90236820 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger and BTB domain-containing protein 10 level in Chronic kidney disease with hypertension and no diabetes (25075_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger and BTB domain-containing protein 10 in blood serum http://purl.obolibrary.org/obo/OBA_2044171 GCST90236821 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Selenium-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (25076_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of methanethiol oxidase in blood serum http://purl.obolibrary.org/obo/OBA_2043423 GCST90236822 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine protease ATG4C level in Chronic kidney disease with hypertension and no diabetes (25078_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine protease ATG4C in blood serum http://purl.obolibrary.org/obo/OBA_2040720 GCST90236823 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-glucuronosyltransferase 2B15 level in Chronic kidney disease with hypertension and no diabetes (25080_16) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of UDP-glucuronosyltransferase 2B15 in blood serum http://purl.obolibrary.org/obo/OBA_2044027 GCST90236824 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neural Wiskott-Aldrich syndrome protein level in Chronic kidney disease with hypertension and no diabetes (25082_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin nucleation-promoting factor WASL in blood serum http://purl.obolibrary.org/obo/OBA_2044125 GCST90236825 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein diaphanous homolog 1 level in Chronic kidney disease with hypertension and no diabetes (25083_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein diaphanous homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041301 GCST90236826 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tether containing UBX domain for GLUT4 level in Chronic kidney disease with hypertension and no diabetes (25085_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tether containing UBX domain for GLUT4 in blood serum http://purl.obolibrary.org/obo/OBA_2040707 GCST90236827 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GRAM domain-containing protein 2B level in Chronic kidney disease with hypertension and no diabetes (25086_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GRAM domain-containing protein 2B in blood serum http://purl.obolibrary.org/obo/OBA_2044305 GCST90236828 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dystrobrevin alpha level in Chronic kidney disease with hypertension and no diabetes (25087_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dystrobrevin alpha in blood serum http://purl.obolibrary.org/obo/OBA_2041373 GCST90236829 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform level in Chronic kidney disease with hypertension and no diabetes (25088_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform in blood serum http://purl.obolibrary.org/obo/OBA_2042876 GCST90236830 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription intermediary factor 1-beta level in Chronic kidney disease with hypertension and no diabetes (25089_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription intermediary factor 1-beta in blood serum http://purl.obolibrary.org/obo/OBA_2043935 GCST90236831 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLIT-ROBO Rho GTPase-activating protein 2 level in Chronic kidney disease with hypertension and no diabetes (25091_83) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SLIT-ROBO Rho GTPase-activating protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043652 GCST90236832 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ATP-dependent RNA helicase DDX1 level in Chronic kidney disease with hypertension and no diabetes (25092_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ATP-dependent RNA helicase DDX1 in blood serum http://purl.obolibrary.org/obo/OBA_2041258 GCST90236833 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vang-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (25093_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Vang-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044080 GCST90236834 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acetyl-coenzyme A synthetase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (25094_9) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of acetyl-coenzyme A synthetase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2040488 GCST90236835 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synphilin-1 level in Chronic kidney disease with hypertension and no diabetes (25095_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synphilin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043566 GCST90236836 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myosin-binding protein C, fast-type level in Chronic kidney disease with hypertension and no diabetes (25096_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin-binding protein C, fast-type in blood serum http://purl.obolibrary.org/obo/OBA_2042474 GCST90236837 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calcium-dependent secretion activator 2 level in Chronic kidney disease with hypertension and no diabetes (25099_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calcium-dependent secretion activator 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040873 GCST90236838 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-Maf-inducing protein level in Chronic kidney disease with hypertension and no diabetes (25100_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-Maf-inducing protein in blood serum http://purl.obolibrary.org/obo/OBA_2041064 GCST90236839 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Elongator complex protein 1 level in Chronic kidney disease with hypertension and no diabetes (25102_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of elongator complex protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042000 GCST90236840 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vacuolar protein sorting-associated protein 53 homolog level in Chronic kidney disease with hypertension and no diabetes (25103_45) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of vacuolar protein sorting-associated protein 53 in blood serum http://purl.obolibrary.org/obo/OBA_2044113 GCST90236841 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor CP2-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (25104_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor CP2-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044436 GCST90236842 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 2A level in Chronic kidney disease with hypertension and no diabetes (25105_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 2A in blood serum http://purl.obolibrary.org/obo/OBA_2041439 GCST90236843 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 2A level in Chronic kidney disease with hypertension and no diabetes (25105_87) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 2A in blood serum http://purl.obolibrary.org/obo/OBA_2041439 GCST90236844 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Arginyl-tRNA--protein transferase 1 level in Chronic kidney disease with hypertension and no diabetes (25108_6) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of arginyl-tRNA--protein transferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040711 GCST90236845 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Exocyst complex component 7 level in Chronic kidney disease with hypertension and no diabetes (25110_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of exocyst complex component 7 in blood serum http://purl.obolibrary.org/obo/OBA_2041524 GCST90236846 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RAD18 level in Chronic kidney disease with hypertension and no diabetes (25111_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RAD18 in blood serum http://purl.obolibrary.org/obo/OBA_2043179 GCST90236847 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosomal protein S6 kinase beta-2 level in Chronic kidney disease with hypertension and no diabetes (25112_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosomal protein S6 kinase beta-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040201 GCST90236848 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TBC1 domain family member 24 level in Chronic kidney disease with hypertension and no diabetes (25114_256) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of TBC1 domain family member 24 in blood serum http://purl.obolibrary.org/obo/OBA_2043786 GCST90236849 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. FH1/FH2 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (25115_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of FH1/FH2 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041582 GCST90236850 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Coiled-coil domain-containing protein 9 level in Chronic kidney disease with hypertension and no diabetes (25116_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of coiled-coil domain-containing protein 9 in blood serum http://purl.obolibrary.org/obo/OBA_2044267 GCST90236851 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. PGM5 level in Chronic kidney disease with hypertension and no diabetes (25117_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphoglucomutase-like protein 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042866 GCST90236852 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nodal modulator 2 level in Chronic kidney disease with hypertension and no diabetes (25121_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nodal modulator 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042604 GCST90236853 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger and BTB domain-containing protein 7A level in Chronic kidney disease with hypertension and no diabetes (25124_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger and BTB domain-containing protein 7A in blood serum http://purl.obolibrary.org/obo/OBA_2044174 GCST90236854 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 and cysteine-rich domain-containing protein level in Chronic kidney disease with hypertension and no diabetes (25125_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH3 and cysteine-rich domain-containing protein in blood serum http://purl.obolibrary.org/obo/OBA_2043687 GCST90236855 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase HECW2 level in Chronic kidney disease with hypertension and no diabetes (25126_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase HECW2 in blood serum http://purl.obolibrary.org/obo/OBA_2041855 GCST90236856 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-B3 level in Chronic kidney disease with hypertension and no diabetes (2514_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-B3 measurement http://www.ebi.ac.uk/efo/EFO_0020358 GCST90236857 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. GDNF family receptor alpha-2 level in Chronic kidney disease with hypertension and no diabetes (2515_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 GDNF family receptor alpha-2 measurement http://www.ebi.ac.uk/efo/EFO_0008138 GCST90236858 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-C motif chemokine 21 level in Chronic kidney disease with hypertension and no diabetes (2516_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 C-C motif chemokine 21 measurement http://www.ebi.ac.uk/efo/EFO_0008048 GCST90236859 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium/potassium-transporting ATPase gamma chain level in Chronic kidney disease with hypertension and no diabetes (25209_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium/potassium-transporting ATPase subunit gamma in blood serum http://purl.obolibrary.org/obo/OBA_2041638 GCST90236860 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide-binding protein G(I)/G(S)/G(O) gamma-12 subunit level in Chronic kidney disease with hypertension and no diabetes (25211_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-12 in blood serum http://purl.obolibrary.org/obo/OBA_2041753 GCST90236861 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitochondrial import inner membrane translocase subunit Tim10 level in Chronic kidney disease with hypertension and no diabetes (25215_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mitochondrial import inner membrane translocase subunit Tim10 in blood serum http://purl.obolibrary.org/obo/OBA_2043852 GCST90236862 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calgranulin A level in Chronic kidney disease with hypertension and no diabetes (25216_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of protein S100-A8 in blood serum http://purl.obolibrary.org/obo/OBA_2043369 GCST90236863 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm protein associated with the nucleus on the X chromosome A level in Chronic kidney disease with hypertension and no diabetes (25217_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm protein associated with the nucleus on the X chromosome A in blood serum http://purl.obolibrary.org/obo/OBA_2043614 GCST90236864 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Signal peptidase complex subunit 1 level in Chronic kidney disease with hypertension and no diabetes (25218_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of signal peptidase complex subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043622 GCST90236865 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich tail protein 1 level in Chronic kidney disease with hypertension and no diabetes (25220_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine-rich tail protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044816 GCST90236866 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ferritin heavy polypeptide-like 17 level in Chronic kidney disease with hypertension and no diabetes (25225_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ferritin heavy polypeptide-like 17 in blood serum http://purl.obolibrary.org/obo/OBA_2041625 GCST90236867 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription elongation factor A protein-like 2 level in Chronic kidney disease with hypertension and no diabetes (25227_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription elongation factor A protein-like 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043805 GCST90236868 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vasorin level in Chronic kidney disease with hypertension and no diabetes (5682_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vasorin in blood serum http://purl.obolibrary.org/obo/OBA_2044082 GCST90238033 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucosidase 2 subunit beta level in Chronic kidney disease with hypertension and no diabetes (5687_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glucosidase 2 subunit beta in blood serum http://purl.obolibrary.org/obo/OBA_2043030 GCST90238034 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cerebellin-4 level in Chronic kidney disease with hypertension and no diabetes (5688_65) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cerebellin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2040915 GCST90238035 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 112 level in Chronic kidney disease with hypertension and no diabetes (5689_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 112 in blood serum http://purl.obolibrary.org/obo/OBA_2041272 GCST90238036 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tuftelin level in Chronic kidney disease with hypertension and no diabetes (5690_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tuftelin in blood serum http://purl.obolibrary.org/obo/OBA_2043960 GCST90238037 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cysteine-rich secretory protein LCCL domain-containing 2 level in Chronic kidney disease with hypertension and no diabetes (5691_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cysteine-rich secretory protein LCCL domain-containing 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041145 GCST90238038 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tumor necrosis factor level in Chronic kidney disease with hypertension and no diabetes (5692_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 tumor necrosis factor measurement http://www.ebi.ac.uk/efo/EFO_0010834 GCST90238039 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lithostathine-1-beta level in Chronic kidney disease with hypertension and no diabetes (5693_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lithostathine-1-beta in blood serum http://purl.obolibrary.org/obo/OBA_2043231 GCST90238040 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SPARC-related modular calcium-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (5694_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 sPARC-related modular calcium-binding protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021868 GCST90238041 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BPI fold-containing family A member 2 level in Chronic kidney disease with hypertension and no diabetes (5695_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of BPI fold-containing family A member 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043639 GCST90238042 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin-X level in Chronic kidney disease with hypertension and no diabetes (5698_60) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of tenascin-X in blood serum http://purl.obolibrary.org/obo/OBA_2043896 GCST90238043 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM189A2 level in Chronic kidney disease with hypertension and no diabetes (5699_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endosomal transmembrane epsin interactor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044437 GCST90238044 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tetranectin level in Chronic kidney disease with hypertension and no diabetes (5701_81) 466 African American individuals NA Illumina [14870897] (imputed) 0 tetranectin measurement http://www.ebi.ac.uk/efo/EFO_0020957 GCST90238045 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Noelin level in Chronic kidney disease with hypertension and no diabetes (5703_26) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of noelin in blood serum http://purl.obolibrary.org/obo/OBA_2042701 GCST90238046 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Granzyme M level in Chronic kidney disease with hypertension and no diabetes (5704_74) 466 African American individuals NA Illumina [14870897] (imputed) 0 granzyme b measurement http://www.ebi.ac.uk/efo/EFO_0020418 GCST90238047 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ETS domain-containing protein Elk-3 level in Chronic kidney disease with hypertension and no diabetes (5707_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ETS domain-containing protein Elk-3 in blood serum http://purl.obolibrary.org/obo/OBA_2041467 GCST90238048 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon lambda-3 level in Chronic kidney disease with hypertension and no diabetes (5713_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interleukin-28B in blood serum http://purl.obolibrary.org/obo/OBA_2040303 GCST90238049 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-6 level in Chronic kidney disease with hypertension and no diabetes (5714_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon alpha-6 in blood serum http://purl.obolibrary.org/obo/OBA_2041981 GCST90238050 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein ABHD14A level in Chronic kidney disease with hypertension and no diabetes (5715_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein ABHD14A in blood serum http://purl.obolibrary.org/obo/OBA_2040458 GCST90238051 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Putative chondrosarcoma-associated gene 1 protein level in Chronic kidney disease with hypertension and no diabetes (5716_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of putative chondrosarcoma-associated gene 1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2044435 GCST90238052 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SH3 and multiple ankyrin repeat domains protein 1 level in Chronic kidney disease with hypertension and no diabetes (13256_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of SH3 and multiple ankyrin repeat domains protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043497 GCST90233844 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein Wnt-5a level in Chronic kidney disease with hypertension and no diabetes (13268_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein Wnt-5a in blood serum http://purl.obolibrary.org/obo/OBA_2044141 GCST90233845 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 113 level in Chronic kidney disease with hypertension and no diabetes (13374_4) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of beta-defensin 113 in blood serum http://purl.obolibrary.org/obo/OBA_2041273 GCST90233846 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptogyrin-3 level in Chronic kidney disease with hypertension and no diabetes (13375_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptogyrin-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043746 GCST90233847 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome b561 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (13377_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of probable transmembrane reductase CYB561D1 in blood serum http://purl.obolibrary.org/obo/OBA_2044746 GCST90233848 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glutaredoxin-like protein C5orf63 level in Chronic kidney disease with hypertension and no diabetes (13378_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of glutaredoxin-like protein C5orf63 in blood serum http://purl.obolibrary.org/obo/OBA_2044813 GCST90233849 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4-galactosyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (13381_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,4-galactosyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040756 GCST90233850 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fumarate hydratase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (13384_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fumarate hydratase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041579 GCST90233851 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF34 level in Chronic kidney disease with hypertension and no diabetes (13386_248) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RNF34 in blood serum http://purl.obolibrary.org/obo/OBA_2043298 GCST90233852 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. ETS homologous factor level in Chronic kidney disease with hypertension and no diabetes (13387_55) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ETS homologous factor in blood serum http://purl.obolibrary.org/obo/OBA_2041436 GCST90233853 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroendocrine convertase 1 level in Chronic kidney disease with hypertension and no diabetes (13388_57) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of neuroendocrine convertase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042805 GCST90233854 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Derlin-1 level in Chronic kidney disease with hypertension and no diabetes (13393_46) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of derlin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041288 GCST90233855 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 4A level in Chronic kidney disease with hypertension and no diabetes (13397_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of defensin beta 4A in blood serum http://purl.obolibrary.org/obo/OBA_2044230 GCST90233856 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RELT-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (13399_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RELT-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043235 GCST90233857 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 2 level in Chronic kidney disease with hypertension and no diabetes (13405_61) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine protease inhibitor Kazal-type 2 in blood serum http://purl.obolibrary.org/obo/OBA_2043630 GCST90233858 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CMRF35-like molecule 6 level in Chronic kidney disease with hypertension and no diabetes (13406_161) 466 African American individuals NA Illumina [14870897] (imputed) 0 CMRF35-like molecule 6 measurement http://www.ebi.ac.uk/efo/EFO_0008086 GCST90233859 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (13408_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0008319 GCST90233860 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase NRDP1 level in Chronic kidney disease with hypertension and no diabetes (13411_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase NRDP1 in blood serum http://purl.obolibrary.org/obo/OBA_2043299 GCST90233861 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 6 level in Chronic kidney disease with hypertension and no diabetes (13412_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WAP four-disulfide core domain protein 6 in blood serum http://purl.obolibrary.org/obo/OBA_2044657 GCST90233862 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 132D level in Chronic kidney disease with hypertension and no diabetes (13416_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 132D in blood serum http://purl.obolibrary.org/obo/OBA_2043872 GCST90233863 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein kish-B level in Chronic kidney disease with hypertension and no diabetes (13421_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein kish-B in blood serum http://purl.obolibrary.org/obo/OBA_2044653 GCST90233864 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ecto-NOX disulfide-thiol exchanger 2 level in Chronic kidney disease with hypertension and no diabetes (13422_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ecto-NOX disulfide-thiol exchanger 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041479 GCST90233865 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Redox-regulatory protein FAM213A level in Chronic kidney disease with hypertension and no diabetes (13423_94) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peroxiredoxin-like 2A in blood serum http://purl.obolibrary.org/obo/OBA_2044595 GCST90233866 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mannosyl-oligosaccharide 1,2-alpha-mannosidase IC level in Chronic kidney disease with hypertension and no diabetes (13427_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of mannosyl-oligosaccharide 1,2-alpha-mannosidase IC in blood serum http://purl.obolibrary.org/obo/OBA_2042277 GCST90233867 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. WAP four-disulfide core domain protein 10A level in Chronic kidney disease with hypertension and no diabetes (13429_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of WAP four-disulfide core domain protein 10A in blood serum http://purl.obolibrary.org/obo/OBA_2044769 GCST90233868 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cartilage intermediate layer protein 1 level in Chronic kidney disease with hypertension and no diabetes (5717_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cartilage intermediate layer protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041030 GCST90238053 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM189A2 level in Chronic kidney disease with hypertension and no diabetes (5719_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of endosomal transmembrane epsin interactor 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044437 GCST90238054 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD226 antigen level in Chronic kidney disease with hypertension and no diabetes (5721_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD226 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020246 GCST90238055 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysosomal Pro-X carboxypeptidase level in Chronic kidney disease with hypertension and no diabetes (5722_78) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lysosomal Pro-X carboxypeptidase in blood serum http://purl.obolibrary.org/obo/OBA_2043018 GCST90238056 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like 3 level in Chronic kidney disease with hypertension and no diabetes (5723_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-like 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042034 GCST90238057 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Suprabasin level in Chronic kidney disease with hypertension and no diabetes (5724_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of suprabasin in blood serum http://purl.obolibrary.org/obo/OBA_2043389 GCST90238058 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteomodulin level in Chronic kidney disease with hypertension and no diabetes (5725_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 osteomodulin measurement http://www.ebi.ac.uk/efo/EFO_0020619 GCST90238059 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm-associated antigen 11A level in Chronic kidney disease with hypertension and no diabetes (5726_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm-associated antigen 11A in blood serum http://purl.obolibrary.org/obo/OBA_2043610 GCST90238060 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,3-glucosyltransferase level in Chronic kidney disease with hypertension and no diabetes (5727_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,3-glucosyltransferase in blood serum http://purl.obolibrary.org/obo/OBA_2040749 GCST90238061 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fc receptor-like protein 1 level in Chronic kidney disease with hypertension and no diabetes (5728_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Fc receptor-like protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041563 GCST90238062 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sclerostin level in Chronic kidney disease with hypertension and no diabetes (5729_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 sclerostin measurement http://www.ebi.ac.uk/efo/EFO_0010606 GCST90238063 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C-X-C motif chemokine 14 level in Chronic kidney disease with hypertension and no diabetes (5730_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C-X-C motif chemokine 14 in blood serum http://purl.obolibrary.org/obo/OBA_2041206 GCST90238064 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine protease inhibitor Kazal-type 6 level in Chronic kidney disease with hypertension and no diabetes (5731_1) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of serine protease inhibitor Kazal-type 6 in blood serum http://purl.obolibrary.org/obo/OBA_2043634 GCST90238065 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon alpha-10 level in Chronic kidney disease with hypertension and no diabetes (5733_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon alpha-10 measurement http://www.ebi.ac.uk/efo/EFO_0021946 GCST90238066 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nectin-4 level in Chronic kidney disease with hypertension and no diabetes (5734_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nectin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043119 GCST90238067 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. C1GALT1-specific chaperone 1 level in Chronic kidney disease with hypertension and no diabetes (5735_54) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of C1GALT1-specific chaperone 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040844 GCST90238068 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trem-like transcript 2 protein level in Chronic kidney disease with hypertension and no diabetes (5736_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trem-like transcript 2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2043928 GCST90238069 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-4D level in Chronic kidney disease with hypertension and no diabetes (5737_61) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-4D in blood serum http://purl.obolibrary.org/obo/OBA_2040387 GCST90238070 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tenascin level in Chronic kidney disease with hypertension and no diabetes (5738_25) 466 African American individuals NA Illumina [14870897] (imputed) 0 tenascin measurement http://www.ebi.ac.uk/efo/EFO_0008296 GCST90238071 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Roundabout homolog 1 level in Chronic kidney disease with hypertension and no diabetes (5740_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of roundabout homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043305 GCST90238072 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eosinophil cationic protein level in Chronic kidney disease with hypertension and no diabetes (5741_55) 466 African American individuals NA Illumina [14870897] (imputed) 1 eosinophil cationic protein measurement http://www.ebi.ac.uk/efo/EFO_0010913 GCST90238073 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lysophosphatidic acid phosphatase type 6 level in Chronic kidney disease with hypertension and no diabetes (5742_14) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of lysophosphatidic acid phosphatase type 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040483 GCST90238074 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cocaine- and amphetamine-regulated transcript protein level in Chronic kidney disease with hypertension and no diabetes (5743_82) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cocaine- and amphetamine-regulated transcript protein in blood serum http://purl.obolibrary.org/obo/OBA_2040902 GCST90238075 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein MENT level in Chronic kidney disease with hypertension and no diabetes (5744_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein MENT in blood serum http://purl.obolibrary.org/obo/OBA_2044886 GCST90238076 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidase inhibitor 15 level in Chronic kidney disease with hypertension and no diabetes (5745_64) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidase inhibitor 15 in blood serum http://purl.obolibrary.org/obo/OBA_2042884 GCST90238077 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Parathyroid hormone level in Chronic kidney disease with hypertension and no diabetes (5954_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 parathyroid hormone measurement http://www.ebi.ac.uk/efo/EFO_0004752 GCST90238128 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Somatostatin-28 level in Chronic kidney disease with hypertension and no diabetes (5957_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 somatostatin-28 measurement http://www.ebi.ac.uk/efo/EFO_0020745 GCST90238129 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Orphan sodium- and chloride-dependent neurotransmitter transporter NTT5 level in Chronic kidney disease with hypertension and no diabetes (13056_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of orphan sodium- and chloride-dependent neurotransmitter transporter NTT5 in blood serum http://purl.obolibrary.org/obo/OBA_2043541 GCST90233796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Riboflavin kinase level in Chronic kidney disease with hypertension and no diabetes (13059_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of riboflavin kinase in blood serum http://purl.obolibrary.org/obo/OBA_2043246 GCST90233797 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Enhancer of mRNA-decapping protein 4 level in Chronic kidney disease with hypertension and no diabetes (13066_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of enhancer of mRNA-decapping protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041409 GCST90233798 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. cGMP-dependent protein kinase 1, beta isozyme level in Chronic kidney disease with hypertension and no diabetes (13067_5) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of cGMP-dependent protein kinase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044242 GCST90233799 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acidic leucine-rich nuclear phosphoprotein 32 family member A level in Chronic kidney disease with hypertension and no diabetes (13073_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acidic leucine-rich nuclear phosphoprotein 32 family member A in blood serum http://purl.obolibrary.org/obo/OBA_2040594 GCST90233800 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fragile X mental retardation syndrome-related protein 1 level in Chronic kidney disease with hypertension and no diabetes (13076_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RNA-binding protein FXR1 in blood serum http://purl.obolibrary.org/obo/OBA_2040441 GCST90233801 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Centrin-2 level in Chronic kidney disease with hypertension and no diabetes (13078_3) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of centrin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040991 GCST90233802 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein unc-45 homolog A level in Chronic kidney disease with hypertension and no diabetes (13082_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein unc-45 homolog A in blood serum http://purl.obolibrary.org/obo/OBA_2044036 GCST90233803 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Valine--tRNA ligase level in Chronic kidney disease with hypertension and no diabetes (13083_18) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of valine--tRNA ligase in blood serum http://purl.obolibrary.org/obo/OBA_2044081 GCST90233804 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glucagon-like peptide 1 receptor level in Chronic kidney disease with hypertension and no diabetes (13085_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 glucagon-like peptide-1 measurement http://www.ebi.ac.uk/efo/EFO_0008465 GCST90233805 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Betacellulin level in Chronic kidney disease with hypertension and no diabetes (13088_397) 466 African American individuals NA Illumina [14870897] (imputed) 0 betacellulin measurement http://www.ebi.ac.uk/efo/EFO_0021883 GCST90233806 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Hypoxia-inducible factor 1-alpha level in Chronic kidney disease with hypertension and no diabetes (13089_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 hypoxia-inducible factor 1-alpha measurement http://www.ebi.ac.uk/efo/EFO_0021926 GCST90233807 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A6 level in Chronic kidney disease with hypertension and no diabetes (13090_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein S100-A6 measurement http://www.ebi.ac.uk/efo/EFO_0021927 GCST90233808 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Secreted and transmembrane protein 1 level in Chronic kidney disease with hypertension and no diabetes (13093_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 secreted and transmembrane protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0021852 GCST90233809 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. R-spondin-3 level in Chronic kidney disease with hypertension and no diabetes (13094_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 r-spondin-3 measurement http://www.ebi.ac.uk/efo/EFO_0021878 GCST90233810 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lithostathine-1-alpha level in Chronic kidney disease with hypertension and no diabetes (13095_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lithostathine-1-alpha in blood serum http://purl.obolibrary.org/obo/OBA_2043230 GCST90233811 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bcl-2-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (13097_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 bcl-2-like protein 2 measurement http://www.ebi.ac.uk/efo/EFO_0021928 GCST90233812 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sclerostin level in Chronic kidney disease with hypertension and no diabetes (13101_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 sclerostin measurement http://www.ebi.ac.uk/efo/EFO_0010606 GCST90233813 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM3D level in Chronic kidney disease with hypertension and no diabetes (13102_1) 466 African American individuals NA Illumina [14870897] (imputed) 2 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90233814 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Chorionic somatomammotropin hormone level in Chronic kidney disease with hypertension and no diabetes (13103_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 chorionic somatomammotropin hormone measurement http://www.ebi.ac.uk/efo/EFO_0021929 GCST90233815 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-B1 level in Chronic kidney disease with hypertension and no diabetes (13104_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-B1 measurement http://www.ebi.ac.uk/efo/EFO_0021930 GCST90233816 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptosomal-associated protein 25 level in Chronic kidney disease with hypertension and no diabetes (13105_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 synaptosomal-associated protein 25 measurement http://www.ebi.ac.uk/efo/EFO_0021858 GCST90233817 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ly6/PLAUR domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (13107_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 Ly6/PLAUR domain-containing protein 3 measurement http://www.ebi.ac.uk/efo/EFO_0021931 GCST90233818 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Osteocalcin level in Chronic kidney disease with hypertension and no diabetes (5747_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 osteocalcin measurement http://www.ebi.ac.uk/efo/EFO_0010232 GCST90238078 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Acid ceramidase level in Chronic kidney disease with hypertension and no diabetes (5748_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of acid ceramidase in blood serum http://purl.obolibrary.org/obo/OBA_2040688 GCST90238079 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Colipase level in Chronic kidney disease with hypertension and no diabetes (5749_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of colipase in blood serum http://purl.obolibrary.org/obo/OBA_2041055 GCST90238080 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. LETM1 domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (5751_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of LETM1 domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042189 GCST90238081 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sushi domain-containing protein 3 level in Chronic kidney disease with hypertension and no diabetes (5752_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sushi domain-containing protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2044418 GCST90238082 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Insulin-like peptide INSL6 level in Chronic kidney disease with hypertension and no diabetes (5754_76) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of insulin-like peptide INSL6 in blood serum http://purl.obolibrary.org/obo/OBA_2042037 GCST90238083 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gastric inhibitory polypeptide level in Chronic kidney disease with hypertension and no diabetes (5755_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gastric inhibitory polypeptide in blood serum http://purl.obolibrary.org/obo/OBA_2041720 GCST90238084 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pappalysin-2 level in Chronic kidney disease with hypertension and no diabetes (5756_66) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pappalysin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2042760 GCST90238085 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroendocrine secretory protein 55 level in Chronic kidney disease with hypertension and no diabetes (5757_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238086 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kallikrein-9 level in Chronic kidney disease with hypertension and no diabetes (5758_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kallikrein-9 in blood serum http://purl.obolibrary.org/obo/OBA_2042129 GCST90238087 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ephrin-A3 level in Chronic kidney disease with hypertension and no diabetes (5759_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 ephrin-A3 measurement http://www.ebi.ac.uk/efo/EFO_0021956 GCST90238088 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm-associated antigen 11B level in Chronic kidney disease with hypertension and no diabetes (5762_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm-associated antigen 11B in blood serum http://purl.obolibrary.org/obo/OBA_2043611 GCST90238089 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 104 level in Chronic kidney disease with hypertension and no diabetes (5763_67) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 104 in blood serum http://purl.obolibrary.org/obo/OBA_2041267 GCST90238090 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Polypeptide N-acetylgalactosaminyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (5764_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of polypeptide N-acetylgalactosaminyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041664 GCST90238091 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-defensin 121 level in Chronic kidney disease with hypertension and no diabetes (5765_53) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-defensin 121 in blood serum http://purl.obolibrary.org/obo/OBA_2041278 GCST90238092 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. alpha-Fetoprotein level in Chronic kidney disease with hypertension and no diabetes (5792_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 alpha fetoprotein measurement http://www.ebi.ac.uk/efo/EFO_0010583 GCST90238093 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. BH3-interacting domain death agonist level in Chronic kidney disease with hypertension and no diabetes (5798_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 BH3-interacting domain death agonist measurement http://www.ebi.ac.uk/efo/EFO_0021994 GCST90238094 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. beta-nerve growth factor level in Chronic kidney disease with hypertension and no diabetes (5801_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 beta-nerve growth factor measurement http://www.ebi.ac.uk/efo/EFO_0008035 GCST90238095 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Complement C3d fragment level in Chronic kidney disease with hypertension and no diabetes (5803_24) 466 African American individuals NA Illumina [14870897] (imputed) 0 complement C3D fragment measurement http://www.ebi.ac.uk/efo/EFO_0020277 GCST90238096 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CD70 antigen level in Chronic kidney disease with hypertension and no diabetes (5807_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 CD70 antigen measurement http://www.ebi.ac.uk/efo/EFO_0020249 GCST90238097 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Teratocarcinoma-derived growth factor 1 level in Chronic kidney disease with hypertension and no diabetes (5810_25) 466 African American individuals NA Illumina [14870897] (imputed) 1 teratocarcinoma-derived growth factor 1 measurement http://www.ebi.ac.uk/efo/EFO_0008297 GCST90238098 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Erythropoietin level in Chronic kidney disease with hypertension and no diabetes (5813_58) 466 African American individuals NA Illumina [14870897] (imputed) 0 erythropoietin measurement http://www.ebi.ac.uk/efo/EFO_0020363 GCST90238099 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Glial cell line-derived neurotrophic factor level in Chronic kidney disease with hypertension and no diabetes (5822_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 glial cell line-derived neurotrophic factor measurement http://www.ebi.ac.uk/efo/EFO_0021887 GCST90238100 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon gamma receptor 1 level in Chronic kidney disease with hypertension and no diabetes (5825_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 interferon gamma receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020484 GCST90238101 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-9 level in Chronic kidney disease with hypertension and no diabetes (5834_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin 9 measurement http://www.ebi.ac.uk/efo/EFO_0008192 GCST90238102 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AarF domain-containing protein kinase 4 level in Chronic kidney disease with hypertension and no diabetes (9794_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of atypical kinase COQ8B, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2044236 GCST90239468 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ceroid-lipofuscinosis neuronal protein 5 level in Chronic kidney disease with hypertension and no diabetes (9795_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239469 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bile salt-activated lipase level in Chronic kidney disease with hypertension and no diabetes (9796_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bile salt-activated lipase in blood serum http://purl.obolibrary.org/obo/OBA_2040985 GCST90239470 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 8, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9800_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 8, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2042545 GCST90239471 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Patatin-like phospholipase domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (9802_27) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of patatin-like phospholipase domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2042954 GCST90239472 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-4B level in Chronic kidney disease with hypertension and no diabetes (9805_51) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-4B in blood serum http://purl.obolibrary.org/obo/OBA_2043431 GCST90239473 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Trinucleotide repeat-containing gene 6B protein level in Chronic kidney disease with hypertension and no diabetes (9808_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of trinucleotide repeat-containing gene 6B protein in blood serum http://purl.obolibrary.org/obo/OBA_2043894 GCST90239474 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GTPase-activating protein 1 level in Chronic kidney disease with hypertension and no diabetes (9815_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 ras GTPase-activating protein 1 measurement http://www.ebi.ac.uk/efo/EFO_0020698 GCST90239475 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Isochorismatase domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9816_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of isochorismatase domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044635 GCST90239476 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Induced myeloid leukemia cell differentiation protein Mcl-1 level in Chronic kidney disease with hypertension and no diabetes (9819_110) 466 African American individuals NA Illumina [14870897] (imputed) 0 induced myeloid leukemia cell differentiation protein Mcl-1 measurement http://www.ebi.ac.uk/efo/EFO_0021910 GCST90239477 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dihydrofolate reductase level in Chronic kidney disease with hypertension and no diabetes (9823_2) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of dihydrofolate reductase in blood serum http://purl.obolibrary.org/obo/OBA_2041401 GCST90239478 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bis(5'-adenosyl)-triphosphatase level in Chronic kidney disease with hypertension and no diabetes (9826_135) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bis(5'-adenosyl)-triphosphatase in blood serum http://purl.obolibrary.org/obo/OBA_2041580 GCST90239479 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. L-lactate dehydrogenase C chain level in Chronic kidney disease with hypertension and no diabetes (9828_86) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of L-lactate dehydrogenase C chain in blood serum http://purl.obolibrary.org/obo/OBA_2042182 GCST90239480 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Bile salt sulfotransferase level in Chronic kidney disease with hypertension and no diabetes (9829_91) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 2A1 in blood serum http://purl.obolibrary.org/obo/OBA_2044361 GCST90239481 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Guanine nucleotide exchange factor VAV3 level in Chronic kidney disease with hypertension and no diabetes (9830_109) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of guanine nucleotide exchange factor VAV3 in blood serum http://purl.obolibrary.org/obo/OBA_2044086 GCST90239482 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homogentisate 1,2-dioxygenase level in Chronic kidney disease with hypertension and no diabetes (9832_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homogentisate 1,2-dioxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2041869 GCST90239483 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alcohol dehydrogenase 1B level in Chronic kidney disease with hypertension and no diabetes (9834_62) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of all-trans-retinol dehydrogenase [NAD(+)] ADH1B in blood serum http://purl.obolibrary.org/obo/OBA_2040514 GCST90239484 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldehyde dehydrogenase family 1 member A3 level in Chronic kidney disease with hypertension and no diabetes (9835_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldehyde dehydrogenase family 1 member A3 in blood serum http://purl.obolibrary.org/obo/OBA_2040560 GCST90239485 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deoxycytidine kinase level in Chronic kidney disease with hypertension and no diabetes (9836_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deoxycytidine kinase in blood serum http://purl.obolibrary.org/obo/OBA_2041239 GCST90239486 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NAD(P)H dehydrogenase [quinone] 1 level in Chronic kidney disease with hypertension and no diabetes (9837_60) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of NAD(P)H dehydrogenase [quinone] 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042626 GCST90239487 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mothers against decapentaplegic homolog 1 level in Chronic kidney disease with hypertension and no diabetes (9838_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of smad1 in blood serum http://purl.obolibrary.org/obo/OBA_2040216 GCST90239488 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Toll/interleukin-1 receptor domain-containing adapter protein level in Chronic kidney disease with hypertension and no diabetes (9839_148) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Toll/interleukin-1 receptor domain-containing adapter protein in blood serum http://purl.obolibrary.org/obo/OBA_2040321 GCST90239489 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cell division control protein 42 homolog level in Chronic kidney disease with hypertension and no diabetes (9840_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cell division control protein 42 in blood serum http://purl.obolibrary.org/obo/OBA_2040953 GCST90239490 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Multifunctional protein ADE2 level in Chronic kidney disease with hypertension and no diabetes (9841_197) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of bifunctional phosphoribosylaminoimidazole carboxylase/phosphoribosylaminoimidazole succinocarboxamide synthetase in blood serum http://purl.obolibrary.org/obo/OBA_2042748 GCST90239491 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catenin beta-1 level in Chronic kidney disease with hypertension and no diabetes (9842_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of catenin beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040402 GCST90239492 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptophan 2,3-dioxygenase level in Chronic kidney disease with hypertension and no diabetes (9880_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tryptophan 2,3-dioxygenase in blood serum http://purl.obolibrary.org/obo/OBA_2043820 GCST90239518 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lactoylglutathione lyase level in Chronic kidney disease with hypertension and no diabetes (9883_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of lactoylglutathione lyase in blood serum http://purl.obolibrary.org/obo/OBA_2041731 GCST90239519 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Peptidyl-prolyl cis-trans isomerase-like 1 level in Chronic kidney disease with hypertension and no diabetes (9884_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of peptidyl-prolyl cis-trans isomerase-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042988 GCST90239520 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ras-related protein Rap-2a level in Chronic kidney disease with hypertension and no diabetes (9885_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Ras-related protein Rap-2a in blood serum http://purl.obolibrary.org/obo/OBA_2043195 GCST90239521 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA repair protein XRCC4 level in Chronic kidney disease with hypertension and no diabetes (9886_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA repair protein XRCC4 in blood serum http://purl.obolibrary.org/obo/OBA_2044153 GCST90239522 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RBBP6 level in Chronic kidney disease with hypertension and no diabetes (9887_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RBBP6 in blood serum http://purl.obolibrary.org/obo/OBA_2043203 GCST90239523 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Actin filament-associated protein 1-like 1 level in Chronic kidney disease with hypertension and no diabetes (9889_42) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of actin filament-associated protein 1-like 1 in blood serum http://purl.obolibrary.org/obo/OBA_2040530 GCST90239524 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomyosin alpha-3 chain level in Chronic kidney disease with hypertension and no diabetes (9890_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tropomyosin alpha-3 chain in blood serum http://purl.obolibrary.org/obo/OBA_2043911 GCST90239525 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ornithine decarboxylase antizyme 1 level in Chronic kidney disease with hypertension and no diabetes (9893_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ornithine decarboxylase antizyme in blood serum http://purl.obolibrary.org/obo/OBA_2042686 GCST90239526 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Unconventional myosin-VI level in Chronic kidney disease with hypertension and no diabetes (9894_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myosin-VI in blood serum http://purl.obolibrary.org/obo/OBA_2042487 GCST90239527 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA repair endonuclease XPF level in Chronic kidney disease with hypertension and no diabetes (9895_77) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA repair endonuclease XPF in blood serum http://purl.obolibrary.org/obo/OBA_2041503 GCST90239528 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA replication licensing factor MCM6 level in Chronic kidney disease with hypertension and no diabetes (9897_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA replication licensing factor MCM6 in blood serum http://purl.obolibrary.org/obo/OBA_2042315 GCST90239529 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. AT-rich interactive domain-containing protein 1A level in Chronic kidney disease with hypertension and no diabetes (9898_161) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of AT-rich interactive domain-containing protein 1A in blood serum http://purl.obolibrary.org/obo/OBA_2040662 GCST90239530 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kinesin-like protein KIF1C level in Chronic kidney disease with hypertension and no diabetes (9899_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of kinesin-like protein KIF1C in blood serum http://purl.obolibrary.org/obo/OBA_2042097 GCST90239531 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neurofilament heavy polypeptide level in Chronic kidney disease with hypertension and no diabetes (9900_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neurofilament heavy polypeptide in blood serum http://purl.obolibrary.org/obo/OBA_2042553 GCST90239532 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Egl nine homolog 1 level in Chronic kidney disease with hypertension and no diabetes (9901_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of egl nine homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041428 GCST90239533 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Testican-3 level in Chronic kidney disease with hypertension and no diabetes (9906_21) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of testican-3 in blood serum http://purl.obolibrary.org/obo/OBA_2043640 GCST90239534 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tankyrase-1 level in Chronic kidney disease with hypertension and no diabetes (9907_216) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of poly [ADP-ribose] polymerase tankyrase-1 in blood serum http://purl.obolibrary.org/obo/OBA_2043891 GCST90239535 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. S-methyl-5'-thioadenosine phosphorylase level in Chronic kidney disease with hypertension and no diabetes (9910_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of S-methyl-5'-thioadenosine phosphorylase in blood serum http://purl.obolibrary.org/obo/OBA_2042446 GCST90239536 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosome-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (9913_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosome-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043345 GCST90239537 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Calbindin level in Chronic kidney disease with hypertension and no diabetes (9918_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of calbindin in blood serum http://purl.obolibrary.org/obo/OBA_2040874 GCST90239538 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Son of sevenless homolog 1 level in Chronic kidney disease with hypertension and no diabetes (9923_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of son of sevenless homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043599 GCST90239539 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Scavenger receptor class F member 2 level in Chronic kidney disease with hypertension and no diabetes (9925_56) 466 African American individuals NA Illumina [14870897] (imputed) 0 scavenger receptor class F member 2 measurement http://www.ebi.ac.uk/efo/EFO_0020716 GCST90239540 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-P level in Chronic kidney disease with hypertension and no diabetes (9926_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein S100-P in blood serum http://purl.obolibrary.org/obo/OBA_2043371 GCST90239541 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tensin-4 level in Chronic kidney disease with hypertension and no diabetes (9927_96) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tensin-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043895 GCST90239542 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive dipeptidyl peptidase 10 level in Chronic kidney disease with hypertension and no diabetes (7890_68) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inactive dipeptidyl peptidase 10 in blood serum http://purl.obolibrary.org/obo/OBA_2041352 GCST90238691 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UDP-glucuronosyltransferase 1-6 level in Chronic kidney disease with hypertension and no diabetes (7891_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of UDP-glucuronosyltransferase 1-6 in blood serum http://purl.obolibrary.org/obo/OBA_2044024 GCST90238692 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM234B level in Chronic kidney disease with hypertension and no diabetes (7892_132) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238693 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Oxidized low-density lipoprotein receptor 1 level in Chronic kidney disease with hypertension and no diabetes (7893_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 oxidized low-density lipoprotein receptor 1 measurement http://www.ebi.ac.uk/efo/EFO_0020620 GCST90238694 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fibroblast growth factor 3 level in Chronic kidney disease with hypertension and no diabetes (7894_155) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fibroblast growth factor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041574 GCST90238695 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Melanocortin-2 receptor accessory protein level in Chronic kidney disease with hypertension and no diabetes (7895_108) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of melanocortin-2 receptor accessory protein in blood serum http://purl.obolibrary.org/obo/OBA_2042412 GCST90238696 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disks large homolog 3 level in Chronic kidney disease with hypertension and no diabetes (7897_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disks large homolog 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041310 GCST90238697 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear protein MDM1 level in Chronic kidney disease with hypertension and no diabetes (7898_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear protein MDM1 in blood serum http://purl.obolibrary.org/obo/OBA_2042319 GCST90238698 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Haptoglobin isoform 2 level in Chronic kidney disease with hypertension and no diabetes (7905_30) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of haptoglobin in blood serum http://purl.obolibrary.org/obo/OBA_2041919 GCST90238699 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sex hormone-binding globulin level in Chronic kidney disease with hypertension and no diabetes (7909_37) 466 African American individuals NA Illumina [14870897] (imputed) 0 sex hormone-binding globulin measurement http://www.ebi.ac.uk/efo/EFO_0004696 GCST90238700 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat and fibronectin type III domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (7910_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat and fibronectin type III domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042225 GCST90238701 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sodium channel subunit beta-4 level in Chronic kidney disease with hypertension and no diabetes (7911_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sodium channel subunit beta-4 in blood serum http://purl.obolibrary.org/obo/OBA_2043406 GCST90238702 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amyloid-like protein 2 level in Chronic kidney disease with hypertension and no diabetes (7915_31) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of amyloid beta precursor like protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040618 GCST90238703 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein S100-A7 level in Chronic kidney disease with hypertension and no diabetes (7916_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein S100-A7 measurement http://www.ebi.ac.uk/efo/EFO_0022002 GCST90238704 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Carboxypeptidase D level in Chronic kidney disease with hypertension and no diabetes (7917_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of carboxypeptidase D in blood serum http://purl.obolibrary.org/obo/OBA_2041116 GCST90238705 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-amylase 1 level in Chronic kidney disease with hypertension and no diabetes (7918_114) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-amylase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044803 GCST90238706 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM3D level in Chronic kidney disease with hypertension and no diabetes (7919_278) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein FAM3D measurement http://www.ebi.ac.uk/efo/EFO_0021869 GCST90238707 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-2,8-sialyltransferase 8B level in Chronic kidney disease with hypertension and no diabetes (7920_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-2,8-sialyltransferase 8B in blood serum http://purl.obolibrary.org/obo/OBA_2043682 GCST90238708 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Four-jointed box protein 1 level in Chronic kidney disease with hypertension and no diabetes (7921_65) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of four-jointed box protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041585 GCST90238709 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Adrenomedullin level in Chronic kidney disease with hypertension and no diabetes (7922_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 adrenomedullin measurement http://www.ebi.ac.uk/efo/EFO_0010909 GCST90238710 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-4C level in Chronic kidney disease with hypertension and no diabetes (7923_41) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-4C in blood serum http://purl.obolibrary.org/obo/OBA_2043432 GCST90238711 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD3 gamma chain level in Chronic kidney disease with hypertension and no diabetes (7924_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD3 gamma in blood serum http://purl.obolibrary.org/obo/OBA_2040230 GCST90238712 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Single-pass membrane and coiled-coil domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (7925_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of single-pass membrane and coiled-coil domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044814 GCST90238713 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Kunitz-type protease inhibitor 3 level in Chronic kidney disease with hypertension and no diabetes (7926_13) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of Kunitz-type protease inhibitor 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043638 GCST90238714 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 level in Chronic kidney disease with hypertension and no diabetes (7927_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043679 GCST90238715 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-actinin-1 level in Chronic kidney disease with hypertension and no diabetes (9843_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-actinin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2040489 GCST90239493 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Alpha-actinin-2 level in Chronic kidney disease with hypertension and no diabetes (9844_138) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of alpha-actinin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2040490 GCST90239494 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein DJ-1 level in Chronic kidney disease with hypertension and no diabetes (9845_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein dj-1 measurement http://www.ebi.ac.uk/efo/EFO_0020670 GCST90239495 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Rho GDP-dissociation inhibitor 2 level in Chronic kidney disease with hypertension and no diabetes (9846_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Rho GDP-dissociation inhibitor 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040656 GCST90239496 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homeobox protein TGIF2 level in Chronic kidney disease with hypertension and no diabetes (9847_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homeobox protein TGIF2 in blood serum http://purl.obolibrary.org/obo/OBA_2043835 GCST90239497 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-H level in Chronic kidney disease with hypertension and no diabetes (9848_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-H in blood serum http://purl.obolibrary.org/obo/OBA_2040935 GCST90239498 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Eukaryotic translation initiation factor 1A, X-chromosomal level in Chronic kidney disease with hypertension and no diabetes (9850_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of eukaryotic translation initiation factor 1A, X-chromosomal in blood serum http://purl.obolibrary.org/obo/OBA_2044539 GCST90239499 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fatty acid-binding protein, adipocyte level in Chronic kidney disease with hypertension and no diabetes (9851_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 fatty acid-binding protein, adipocyte measurement http://www.ebi.ac.uk/efo/EFO_0010914 GCST90239500 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon-induced protein with tetratricopeptide repeats 2 level in Chronic kidney disease with hypertension and no diabetes (9853_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon-induced protein with tetratricopeptide repeats 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044313 GCST90239501 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Aldose reductase level in Chronic kidney disease with hypertension and no diabetes (9854_36) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of aldo-keto reductase family 1 member B1 in blood serum http://purl.obolibrary.org/obo/OBA_2040547 GCST90239502 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transforming protein RhoA level in Chronic kidney disease with hypertension and no diabetes (9855_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of GTP-binding protein RhoA in blood serum http://purl.obolibrary.org/obo/OBA_2040208 GCST90239503 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 4 level in Chronic kidney disease with hypertension and no diabetes (9857_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon regulatory factor 4 in blood serum http://purl.obolibrary.org/obo/OBA_2040376 GCST90239504 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Diamine acetyltransferase 1 level in Chronic kidney disease with hypertension and no diabetes (9859_180) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of diamine acetyltransferase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043385 GCST90239505 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tropomyosin alpha-4 chain level in Chronic kidney disease with hypertension and no diabetes (9863_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 tropomyosin alpha-4 chain measurement http://www.ebi.ac.uk/efo/EFO_0022015 GCST90239506 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ubiquitin-conjugating enzyme E2 B level in Chronic kidney disease with hypertension and no diabetes (9865_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ubiquitin-conjugating enzyme E2 B in blood serum http://purl.obolibrary.org/obo/OBA_2043990 GCST90239507 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fructose-1,6-bisphosphatase isozyme 2 level in Chronic kidney disease with hypertension and no diabetes (9867_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fructose-1,6-bisphosphatase isozyme 2 in blood serum http://purl.obolibrary.org/obo/OBA_2041556 GCST90239508 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear factor NF-kappa-B p105 subunit level in Chronic kidney disease with hypertension and no diabetes (9869_28) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of nuclear factor NF-kappa-B p105 subunit in blood serum http://purl.obolibrary.org/obo/OBA_2040323 GCST90239509 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Tryptophan--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes (9870_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of tryptophan--tRNA ligase, cytoplasmic in blood serum http://purl.obolibrary.org/obo/OBA_2044122 GCST90239510 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Catenin alpha-2 level in Chronic kidney disease with hypertension and no diabetes (9872_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of catenin alpha-2 in blood serum http://purl.obolibrary.org/obo/OBA_2041187 GCST90239511 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Steroid hormone receptor ERR1 level in Chronic kidney disease with hypertension and no diabetes (9873_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of steroid hormone receptor ERR1 in blood serum http://purl.obolibrary.org/obo/OBA_2041513 GCST90239512 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cyclin-dependent kinase 4 inhibitor B level in Chronic kidney disease with hypertension and no diabetes (9874_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cyclin-dependent kinase 4 inhibitor B in blood serum http://purl.obolibrary.org/obo/OBA_2040194 GCST90239513 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. THO complex subunit 1 level in Chronic kidney disease with hypertension and no diabetes (9875_107) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of THO complex subunit 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043842 GCST90239514 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Fructose-bisphosphate aldolase C level in Chronic kidney disease with hypertension and no diabetes (9876_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of fructose-bisphosphate aldolase C in blood serum http://purl.obolibrary.org/obo/OBA_2040568 GCST90239515 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Crk-like protein level in Chronic kidney disease with hypertension and no diabetes (9877_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Crk-like protein in blood serum http://purl.obolibrary.org/obo/OBA_2041146 GCST90239516 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Estrogen sulfotransferase level in Chronic kidney disease with hypertension and no diabetes (9878_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sulfotransferase 1E1 in blood serum http://purl.obolibrary.org/obo/OBA_2044790 GCST90239517 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclease-sensitive element-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (9751_72) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of Y-box-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044159 GCST90239443 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ezrin level in Chronic kidney disease with hypertension and no diabetes (9753_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ezrin in blood serum http://purl.obolibrary.org/obo/OBA_2040233 GCST90239444 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Ribosyldihydronicotinamide dehydrogenase [quinone] level in Chronic kidney disease with hypertension and no diabetes (9754_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of ribosyldihydronicotinamide dehydrogenase [quinone] in blood serum http://purl.obolibrary.org/obo/OBA_2042627 GCST90239445 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transgelin level in Chronic kidney disease with hypertension and no diabetes (9756_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transgelin in blood serum http://purl.obolibrary.org/obo/OBA_2043772 GCST90239446 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein enabled homolog level in Chronic kidney disease with hypertension and no diabetes (9757_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein enabled in blood serum http://purl.obolibrary.org/obo/OBA_2041475 GCST90239447 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 40S ribosomal protein S4, X isoform level in Chronic kidney disease with hypertension and no diabetes (9758_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of 40S ribosomal protein S4, X isoform in blood serum http://purl.obolibrary.org/obo/OBA_2043336 GCST90239448 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Indoleamine 2,3-dioxygenase 1 level in Chronic kidney disease with hypertension and no diabetes (9759_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of indoleamine 2,3-dioxygenase 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042026 GCST90239449 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Mitogen-activated protein kinase 9 level in Chronic kidney disease with hypertension and no diabetes (9760_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 mitogen-activated protein kinase 9 measurement http://www.ebi.ac.uk/efo/EFO_0020581 GCST90239450 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Vasodilator-stimulated phosphoprotein level in Chronic kidney disease with hypertension and no diabetes (9762_14) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of vasodilator-stimulated phosphoprotein in blood serum http://purl.obolibrary.org/obo/OBA_2044083 GCST90239451 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Heterogeneous nuclear ribonucleoprotein F level in Chronic kidney disease with hypertension and no diabetes (9764_79) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of heterogeneous nuclear ribonucleoprotein F in blood serum http://purl.obolibrary.org/obo/OBA_2041906 GCST90239452 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear distribution protein nudE homolog 1 level in Chronic kidney disease with hypertension and no diabetes (9765_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear distribution protein nudE homolog 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042533 GCST90239453 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein ripply1 level in Chronic kidney disease with hypertension and no diabetes (9767_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein ripply1 in blood serum http://purl.obolibrary.org/obo/OBA_2043277 GCST90239454 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interleukin-10 receptor subunit alpha level in Chronic kidney disease with hypertension and no diabetes (9768_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 interleukin-10 receptor subunit alpha measurement http://www.ebi.ac.uk/efo/EFO_0021890 GCST90239455 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta and Notch-like epidermal growth factor-related receptor level in Chronic kidney disease with hypertension and no diabetes (9769_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239456 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-2 level in Chronic kidney disease with hypertension and no diabetes (9772_153) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239457 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF149 level in Chronic kidney disease with hypertension and no diabetes (9773_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RNF149 in blood serum http://purl.obolibrary.org/obo/OBA_2043293 GCST90239458 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 150 level in Chronic kidney disease with hypertension and no diabetes (9774_59) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RING finger protein 150 in blood serum http://purl.obolibrary.org/obo/OBA_2043294 GCST90239459 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 52B level in Chronic kidney disease with hypertension and no diabetes (9778_45) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 52B in blood serum http://purl.obolibrary.org/obo/OBA_2044773 GCST90239460 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 2 protein level in Chronic kidney disease with hypertension and no diabetes (9779_63) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 2 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041859 GCST90239461 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily C member 11 level in Chronic kidney disease with hypertension and no diabetes (9783_75) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DnaJ homolog subfamily C member 11 in blood serum http://purl.obolibrary.org/obo/OBA_2044695 GCST90239462 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Radiation-inducible immediate-early gene IEX-1 level in Chronic kidney disease with hypertension and no diabetes (9786_310) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of radiation-inducible immediate-early gene IEX-1 in blood serum http://purl.obolibrary.org/obo/OBA_2041974 GCST90239463 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Collectin-12 level in Chronic kidney disease with hypertension and no diabetes (9787_23) 466 African American individuals NA Illumina [14870897] (imputed) 0 collectin-12 measurement http://www.ebi.ac.uk/efo/EFO_0020272 GCST90239464 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nesprin-2 level in Chronic kidney disease with hypertension and no diabetes (9789_52) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nesprin-2 in blood serum http://purl.obolibrary.org/obo/OBA_2043745 GCST90239465 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Serine/threonine-protein kinase BRSK2 level in Chronic kidney disease with hypertension and no diabetes (9790_28) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of serine/threonine-protein kinase BRSK2 in blood serum http://purl.obolibrary.org/obo/OBA_2040830 GCST90239466 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Immunoglobulin superfamily DCC subclass member 4 level in Chronic kidney disease with hypertension and no diabetes (9793_145) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of immunoglobulin superfamily DCC subclass member 4 in blood serum http://purl.obolibrary.org/obo/OBA_2044684 GCST90239467 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Neuroligin-1 level in Chronic kidney disease with hypertension and no diabetes (8052_115) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of neuroligin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042588 GCST90238791 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DnaJ homolog subfamily B member 14 level in Chronic kidney disease with hypertension and no diabetes (8053_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238792 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Integral membrane protein DGCR2/IDD level in Chronic kidney disease with hypertension and no diabetes (8055_33) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of integral membrane protein DGCR2/IDD in blood serum http://purl.obolibrary.org/obo/OBA_2041291 GCST90238793 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Thrombopoietin level in Chronic kidney disease with hypertension and no diabetes (8059_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 thrombopoietin measurement http://www.ebi.ac.uk/efo/EFO_0022004 GCST90238794 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Pro-neuregulin-2, membrane-bound isoform level in Chronic kidney disease with hypertension and no diabetes (8060_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of pro-neuregulin-2, membrane-bound isoform in blood serum http://purl.obolibrary.org/obo/OBA_2042637 GCST90238795 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM171B level in Chronic kidney disease with hypertension and no diabetes (8061_102) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238796 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein eva-1 homolog B level in Chronic kidney disease with hypertension and no diabetes (8062_15) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein eva-1 homolog B in blood serum http://purl.obolibrary.org/obo/OBA_2044501 GCST90238797 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Poliovirus receptor level in Chronic kidney disease with hypertension and no diabetes (8064_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of poliovirus receptor in blood serum http://purl.obolibrary.org/obo/OBA_2040384 GCST90238798 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Prostate and testis expressed protein 4 level in Chronic kidney disease with hypertension and no diabetes (8065_245) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of prostate and testis expressed protein 4 in blood serum http://purl.obolibrary.org/obo/OBA_2042767 GCST90238799 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Synaptotagmin-9 level in Chronic kidney disease with hypertension and no diabetes (8066_38) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of synaptotagmin-9 in blood serum http://purl.obolibrary.org/obo/OBA_2043759 GCST90238800 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Potassium voltage-gated channel subfamily E member 3 level in Chronic kidney disease with hypertension and no diabetes (8067_21) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of potassium voltage-gated channel subfamily E member 3 in blood serum http://purl.obolibrary.org/obo/OBA_2042088 GCST90238801 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Uncharacterized family 31 glucosidase KIAA1161 level in Chronic kidney disease with hypertension and no diabetes (8068_43) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90238802 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. T-cell surface glycoprotein CD3 epsilon chain level in Chronic kidney disease with hypertension and no diabetes (8069_85) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CD3 epsilon in blood serum http://purl.obolibrary.org/obo/OBA_2040229 GCST90238803 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disks large homolog 4 level in Chronic kidney disease with hypertension and no diabetes (8070_88) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of disks large homolog 4 in blood serum http://purl.obolibrary.org/obo/OBA_2041311 GCST90238804 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. SLAM family member 5 level in Chronic kidney disease with hypertension and no diabetes (8073_3) 466 African American individuals NA Illumina [14870897] (imputed) 0 SLAM family member 5 measurement http://www.ebi.ac.uk/efo/EFO_0020741 GCST90238805 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 70, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (8074_32) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 70, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043876 GCST90238806 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sperm acrosome membrane-associated protein 3 level in Chronic kidney disease with hypertension and no diabetes (8076_4) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sperm acrosome membrane-associated protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2043608 GCST90238807 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EP300-interacting inhibitor of differentiation 3 level in Chronic kidney disease with hypertension and no diabetes (8079_39) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of EP300-interacting inhibitor of differentiation 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041437 GCST90238808 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Sushi domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9582_93) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of sushi domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2044564 GCST90239411 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 24 level in Chronic kidney disease with hypertension and no diabetes (9583_17) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of RING finger protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2043295 GCST90239412 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CXADR-like membrane protein level in Chronic kidney disease with hypertension and no diabetes (9585_80) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239413 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cytochrome c oxidase subunit 7A-related protein, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9590_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cytochrome c oxidase subunit 7A-related protein, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041110 GCST90239414 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc transporter 5 level in Chronic kidney disease with hypertension and no diabetes (9594_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of proton-coupled zinc antiporter SLC30A5 in blood serum http://purl.obolibrary.org/obo/OBA_2043534 GCST90239415 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Beta-1,4-galactosyltransferase 2 level in Chronic kidney disease with hypertension and no diabetes (9595_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of beta-1,4-galactosyltransferase 2 in blood serum http://purl.obolibrary.org/obo/OBA_2040757 GCST90239416 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUB and sushi domain-containing protein 1 level in Chronic kidney disease with hypertension and no diabetes (9598_23) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of CUB and sushi domain-containing protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2041168 GCST90239417 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leukocyte cell-derived chemotaxin 1 level in Chronic kidney disease with hypertension and no diabetes (9928_125) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of chondromodulin-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042186 GCST90239543 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. 3-keto-steroid reductase level in Chronic kidney disease with hypertension and no diabetes (9929_16) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239544 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gamma-aminobutyric acid type B receptor subunit 2 level in Chronic kidney disease with hypertension and no diabetes (9930_48) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239545 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Keratin, type II cytoskeletal 1 level in Chronic kidney disease with hypertension and no diabetes (9931_20) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of keratin, type II cytoskeletal 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042137 GCST90239546 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Semaphorin-4F level in Chronic kidney disease with hypertension and no diabetes (9932_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of semaphorin-4F in blood serum http://purl.obolibrary.org/obo/OBA_2043433 GCST90239547 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein ATP1B4 level in Chronic kidney disease with hypertension and no diabetes (9933_49) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein ATP1B4 in blood serum http://purl.obolibrary.org/obo/OBA_2040727 GCST90239548 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Phosphatidylinositol transfer protein alpha isoform level in Chronic kidney disease with hypertension and no diabetes (9934_29) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of phosphatidylinositol transfer protein alpha isoform in blood serum http://purl.obolibrary.org/obo/OBA_2042901 GCST90239549 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase LNX level in Chronic kidney disease with hypertension and no diabetes (9936_27) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase LNX in blood serum http://purl.obolibrary.org/obo/OBA_2042216 GCST90239550 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Gap junction alpha-1 protein level in Chronic kidney disease with hypertension and no diabetes (9937_7) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of gap junction alpha-1 protein in blood serum http://purl.obolibrary.org/obo/OBA_2041826 GCST90239551 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Dual specificity phosphatase 28 level in Chronic kidney disease with hypertension and no diabetes (9940_35) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of dual specificity phosphatase 28 in blood serum http://purl.obolibrary.org/obo/OBA_2041387 GCST90239552 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin beta-1 level in Chronic kidney disease with hypertension and no diabetes (9941_70) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin beta-1 in blood serum http://purl.obolibrary.org/obo/OBA_2042789 GCST90239553 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. NTF2-related export protein 1 level in Chronic kidney disease with hypertension and no diabetes (9942_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of NTF2-related export protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2042683 GCST90239554 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Armadillo repeat-containing protein 5 level in Chronic kidney disease with hypertension and no diabetes (9945_8) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239555 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. DNA topoisomerase 2-binding protein 1 level in Chronic kidney disease with hypertension and no diabetes (9947_22) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of DNA topoisomerase 2-binding protein 1 in blood serum http://purl.obolibrary.org/obo/OBA_2043902 GCST90239556 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Lymphocyte activation gene 3 protein level in Chronic kidney disease with hypertension and no diabetes (9950_229) 466 African American individuals NA Illumina [14870897] (imputed) 0 lymphocyte activation gene 3 protein measurement http://www.ebi.ac.uk/efo/EFO_0020540 GCST90239557 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. F-box/LRR-repeat protein 4 level in Chronic kidney disease with hypertension and no diabetes (9951_36) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239558 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transcription factor A, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9952_57) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transcription factor A, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2043830 GCST90239559 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Nuclear pore complex-interacting protein family member B3 level in Chronic kidney disease with hypertension and no diabetes (9954_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of nuclear pore complex-interacting protein family member B3 in blood serum http://purl.obolibrary.org/obo/OBA_2044517 GCST90239560 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. RING finger protein 148 level in Chronic kidney disease with hypertension and no diabetes (9955_40) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239561 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Disintegrin and metalloproteinase domain-containing protein 15 level in Chronic kidney disease with hypertension and no diabetes (9956_7) 466 African American individuals NA Illumina [14870897] (imputed) 1 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239562 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. E3 ubiquitin-protein ligase RNF114 level in Chronic kidney disease with hypertension and no diabetes (9957_9) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of E3 ubiquitin-protein ligase RNF114 in blood serum http://purl.obolibrary.org/obo/OBA_2043288 GCST90239563 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Transmembrane protein 59-like level in Chronic kidney disease with hypertension and no diabetes (9959_60) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of transmembrane protein 59-like in blood serum http://purl.obolibrary.org/obo/OBA_2043875 GCST90239564 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. TBC1 domain family member 5 level in Chronic kidney disease with hypertension and no diabetes (9960_2) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of TBC1 domain family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2043788 GCST90239565 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Cadherin-related family member 5 level in Chronic kidney disease with hypertension and no diabetes (9962_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of cadherin-related family member 5 in blood serum http://purl.obolibrary.org/obo/OBA_2042462 GCST90239566 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protocadherin beta-10 level in Chronic kidney disease with hypertension and no diabetes (9963_19) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protocadherin beta-10 in blood serum http://purl.obolibrary.org/obo/OBA_2042790 GCST90239567 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Myocardial zonula adherens protein level in Chronic kidney disease with hypertension and no diabetes (9964_10) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of myocardial zonula adherens protein in blood serum http://purl.obolibrary.org/obo/OBA_2044333 GCST90239568 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Solute carrier family 22 member 16 level in Chronic kidney disease with hypertension and no diabetes (9969_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of solute carrier family 22 member 16 in blood serum http://purl.obolibrary.org/obo/OBA_2043527 GCST90239569 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. CUB and sushi domain-containing protein 2 level in Chronic kidney disease with hypertension and no diabetes (9971_5) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of CUB and sushi domain-containing protein 2 in blood serum http://purl.obolibrary.org/obo/OBA_2044566 GCST90239570 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Delta-like protein 3 level in Chronic kidney disease with hypertension and no diabetes (9974_8) 466 African American individuals NA Illumina [14870897] (imputed) 1 level of delta-like protein 3 in blood serum http://purl.obolibrary.org/obo/OBA_2041315 GCST90239571 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Amphoterin-induced protein 1 level in Chronic kidney disease with hypertension and no diabetes (9979_13) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239572 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein FAM234B level in Chronic kidney disease with hypertension and no diabetes (9981_18) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239573 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Inactive serine protease 35 level in Chronic kidney disease with hypertension and no diabetes (9983_97) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of inactive serine protease 35 in blood serum http://purl.obolibrary.org/obo/OBA_2043047 GCST90239574 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Protein YIPF6 level in Chronic kidney disease with hypertension and no diabetes (9984_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of protein YIPF6 in blood serum http://purl.obolibrary.org/obo/OBA_2044162 GCST90239575 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 25 level in Chronic kidney disease with hypertension and no diabetes (9987_30) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239576 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Leucine-rich repeat-containing protein 24 level in Chronic kidney disease with hypertension and no diabetes (9989_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of leucine-rich repeat-containing protein 24 in blood serum http://purl.obolibrary.org/obo/OBA_2044643 GCST90239577 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. EMILIN-3 level in Chronic kidney disease with hypertension and no diabetes (9991_112) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239578 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Zinc finger protein 264 level in Chronic kidney disease with hypertension and no diabetes (9993_11) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of zinc finger protein 264 in blood serum http://purl.obolibrary.org/obo/OBA_2044197 GCST90239579 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial level in Chronic kidney disease with hypertension and no diabetes (9995_6) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial in blood serum http://purl.obolibrary.org/obo/OBA_2041390 GCST90239580 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. UBX domain-containing protein 4 level in Chronic kidney disease with hypertension and no diabetes (9997_12) 466 African American individuals NA Illumina [14870897] (imputed) 0 protein measurement http://www.ebi.ac.uk/efo/EFO_0004747 GCST90239581 Genome-wide genotyping array 2023-06-23 35870639 Surapaneni A 2022-07-21 Kidney Int www.ncbi.nlm.nih.gov/pubmed/35870639 Identification of 969 protein quantitative trait loci in an African American population with kidney disease attributed to hypertension. Interferon regulatory factor 6 level in Chronic kidney disease with hypertension and no diabetes (9999_1) 466 African American individuals NA Illumina [14870897] (imputed) 0 level of interferon regulatory factor 6 in blood serum http://purl.obolibrary.org/obo/OBA_2040378 GCST90239582 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. High density lipoprotein cholesterol levels 40,963 South Asian ancestry individuals NA NR [52000000] (imputed) 17 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90239654 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. High density lipoprotein cholesterol levels 40,963 South Asian ancestry individuals, 48,057 Hispanic individuals, 99,432 Admixed African or African ancestry individuals, 146,492 East Asian ancestry individuals, 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 562 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90239649 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. High density lipoprotein cholesterol levels 99,432 Admixed African or African ancestry individuals NA NR [52000000] (imputed) 52 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90239650 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. High density lipoprotein cholesterol levels 146,492 East Asian ancestry individuals NA NR [52000000] (imputed) 54 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90239651 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. High density lipoprotein cholesterol levels 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 380 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90239652 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. High density lipoprotein cholesterol levels 48,057 Hispanic individuals NA NR [52000000] (imputed) 21 high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004612 GCST90239653 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Triglyceride levels 40,963 South Asian ancestry individuals NA NR [52000000] (imputed) 15 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90239666 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Low density lipoprotein cholesterol levels 99,432 Admixed African or African ancestry individuals NA NR [52000000] (imputed) 55 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90239656 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Low density lipoprotein cholesterol levels 146,492 East Asian ancestry individuals NA NR [52000000] (imputed) 40 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90239657 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Low density lipoprotein cholesterol levels 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 403 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90239658 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Non-HDL cholesterol levels 40,963 South Asian ancestry individuals, 48,057 Hispanic individuals, 99,432 Admixed African or African ancestry individuals, 146,492 East Asian ancestry individuals, 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 404 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90239667 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Low density lipoprotein cholesterol levels 48,057 Hispanic individuals NA NR [52000000] (imputed) 18 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90239659 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Non-HDL cholesterol levels 99,432 Admixed African or African ancestry individuals NA NR [52000000] (imputed) 17 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90239668 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Non-HDL cholesterol levels 146,492 East Asian ancestry individuals NA NR [52000000] (imputed) 57 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90239669 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Low density lipoprotein cholesterol levels 40,963 South Asian ancestry individuals NA NR [52000000] (imputed) 13 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90239660 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Non-HDL cholesterol levels 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 355 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90239670 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Non-HDL cholesterol levels 48,057 Hispanic individuals NA NR [52000000] (imputed) 15 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90239671 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Non-HDL cholesterol levels 40,963 South Asian ancestry individuals NA NR [52000000] (imputed) 13 non-high density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0005689 GCST90239672 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Total cholesterol levels 40,963 South Asian ancestry individuals, 48,057 Hispanic individuals, 99,432 Admixed African or African ancestry individuals, 146,492 East Asian ancestry individuals, 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 511 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90239673 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Total cholesterol levels 99,432 Admixed African or African ancestry individuals NA NR [52000000] (imputed) 73 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90239674 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Total cholesterol levels 146,492 East Asian ancestry individuals NA NR [52000000] (imputed) 76 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90239675 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Total cholesterol levels 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 429 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90239676 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Total cholesterol levels 48,057 Hispanic individuals NA NR [52000000] (imputed) 28 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90239677 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Total cholesterol levels 40,963 South Asian ancestry individuals NA NR [52000000] (imputed) 16 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90239678 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Triglyceride levels 40,963 South Asian ancestry individuals, 48,057 Hispanic individuals, 99,432 Admixed African or African ancestry individuals, 146,492 East Asian ancestry individuals, 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 480 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90239661 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Triglyceride levels 99,432 Admixed African or African ancestry individuals NA NR [52000000] (imputed) 35 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90239662 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Triglyceride levels 146,492 East Asian ancestry individuals NA NR [52000000] (imputed) 27 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90239663 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Triglyceride levels 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 388 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90239664 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Triglyceride levels 48,057 Hispanic individuals NA NR [52000000] (imputed) 27 triglyceride measurement http://www.ebi.ac.uk/efo/EFO_0004530 GCST90239665 Genome-wide genotyping array 2022-11-17 34887591 Graham SE 2021-12-09 Nature www.ncbi.nlm.nih.gov/pubmed/34887591 The power of genetic diversity in genome-wide association studies of lipids. Low density lipoprotein cholesterol levels 40,963 South Asian ancestry individuals, 48,057 Hispanic individuals, 99,432 Admixed African or African ancestry individuals, 146,492 East Asian ancestry individuals, 1,320,016 European ancestry individuals NA NR [52000000] (imputed) 442 low density lipoprotein cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004611 GCST90239655 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2918) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279037 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2924) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279038 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2926) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279039 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2930) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279040 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3002) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279054 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3013) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279055 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3014) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279056 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3015) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279057 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3016) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279058 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3017) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279059 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3018) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279060 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1822) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279776 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1830) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279777 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1845) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279778 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_185) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279779 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1861) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279780 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1866) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279781 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1873) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279782 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1877) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 39 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279783 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1884) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279784 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1888) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279785 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1890) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279786 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1907) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279787 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1914) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 185 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279788 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1918) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279789 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3543) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279159 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3551) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279160 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3561) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279161 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3562) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279162 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3568) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279163 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_357) (N-Acryloylglycine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279164 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3577) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279165 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_358) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279166 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3582) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279167 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3584) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279168 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3587) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279169 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_359) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279170 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3590) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279171 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3591) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279172 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3592) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279173 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3596) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279174 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_36) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279175 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3611) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279176 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3620) (1-O-alpha-D-glucopyranosyl-12-nonadecandiol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of 1-O-alpha-D-Glucopyranosyl-1,2-nonadecandiol in blood serum http://purl.obolibrary.org/obo/OBA_2045041 GCST90279177 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3622) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279178 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3626) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279179 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3633) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 25 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279180 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2533) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279892 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2537) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279893 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2541) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279894 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2278) (Kynurenine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90279855 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2285) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279856 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2292) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279857 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2293) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279858 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2295) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279859 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_231) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279860 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2313) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279861 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2325) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279862 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2326) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279863 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2333) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279864 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2351) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279865 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2363) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279866 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2366) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279867 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2370) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279868 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2372) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279869 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2373) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279870 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2377) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279871 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2394) (12-aminolauramide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of 12-aminododecanoic acid in blood serum http://purl.obolibrary.org/obo/OBA_2045053 GCST90279872 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2399) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279873 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2404) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279874 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_245) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279875 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2457) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279876 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2464) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279877 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2468) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279878 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2473) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279879 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3318) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279118 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3335) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279119 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3338) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279120 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2155) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279833 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2165) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 16 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279834 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2172) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279835 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2179) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279836 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2181) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279837 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2183) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279838 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_219) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279839 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2196) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279840 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2199) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279841 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_22) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279842 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2200) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279843 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2201) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279844 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2210) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279845 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2216) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279846 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2218) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279847 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2223) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279848 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2228) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279849 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2230) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279850 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2232) (S-nirvanol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279851 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_224) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279852 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2240) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279853 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2249) (L-Tryptophan) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 L-Tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021633 GCST90279854 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3053) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279068 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3056) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279069 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3057) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279070 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3066) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279071 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3069) (Tribromodibenzofuran) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tribromodibenzofuran measurement http://www.ebi.ac.uk/efo/EFO_0803530 GCST90279072 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3071) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279073 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3076) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279074 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3078) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279075 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3087) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279076 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3088) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279077 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3098) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279078 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3108) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279079 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_311) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279080 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3111) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279081 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3118) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279082 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3120) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279083 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3121) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279084 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3128) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279085 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3133) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279086 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3158) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279087 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3163) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279088 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3175) (Fenasulam) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 fenasulam measurement http://www.ebi.ac.uk/efo/EFO_0803526 GCST90279089 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3179) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279090 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3188) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279091 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3199) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279092 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_341) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279134 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3412) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279135 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3419) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279136 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3420) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279137 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3424) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279138 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_343) (Pyrrolidonecarboxylic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279139 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3434) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279140 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3441) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279141 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3448) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279142 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3450) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279143 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3469) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279144 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3482) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279145 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3494) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279146 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3497) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279147 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3500) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279148 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3503) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279149 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3517) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279150 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3522) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279151 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3527) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279152 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3529) (Rhodojaponin I) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279153 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3532) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279154 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3535) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279155 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3536) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279156 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3539) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279157 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3541) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279158 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3201) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279093 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3204) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279094 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3206) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279095 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3207) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279096 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3208) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279097 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3209) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279098 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3212) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279099 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3215) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279100 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3220) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279101 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3221) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279102 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3237) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279103 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3247) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279104 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3254) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279105 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3260) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279106 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3261) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279107 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3273) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279108 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3276) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279109 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_328) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279110 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3281) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279111 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3282) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279112 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3291) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279113 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3303) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279114 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3304) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279115 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3312) (Adenosine diphosphate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90279116 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3317) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279117 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2476) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279880 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2478) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279881 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_248) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279882 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2483) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279883 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2497) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279884 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2505) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279885 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2511) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279886 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2516) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279887 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_252) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279888 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2525) (Buthionine sulfoximine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279889 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2528) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279890 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2532) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279891 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_334) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279121 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3341) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279122 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3342) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279123 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3347) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279124 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3354) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279125 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3355) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279126 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3369) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279127 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3371) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279128 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3389) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279129 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_339) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279130 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_34) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279131 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3405) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279132 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3407) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279133 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2066) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279815 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2067) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279816 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2068) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279817 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2071) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279818 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2078) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279819 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2085) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279820 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2092) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279821 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2096) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279822 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2105) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279823 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2109) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279824 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2118) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279825 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_212) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279826 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2124) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279827 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2128) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279828 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2129) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279829 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2142) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279830 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2144) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279831 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2150) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279832 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_302) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279061 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3029) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279062 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3032) (Tridihexethyl bromide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tridihexethyl bromide measurement http://www.ebi.ac.uk/efo/EFO_0803520 GCST90279063 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3033) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279064 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3046) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279065 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3048) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279066 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3051) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279067 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C12H22O4 (1) levels 44 African ancestry individuals NA Affymetrix [7561079] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201568 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) measurement http://www.ebi.ac.uk/efo/EFO_0800566 GCST90201569 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Heptenedioate (C7:1-DC) levels 59 African ancestry individuals NA Affymetrix [7496246] (imputed) 0 heptenedioate (C7:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800564 GCST90201570 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxyasparagine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 hydroxyasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800092 GCST90201571 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxybutyroylglycine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxybutyroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800568 GCST90201572 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanoate (PFOA) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 perfluorooctanoate (PFOA) measurement http://www.ebi.ac.uk/efo/EFO_0801024 GCST90201573 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C7H12O2 levels 50 African ancestry individuals NA Affymetrix [7375268] (imputed) 0 glutamine conjugate of C7H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800656 GCST90201574 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-formylindole levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90201575 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H12O2 levels 46 African ancestry individuals NA Affymetrix [7718967] (imputed) 0 glycine conjugate of C10H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800654 GCST90201576 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminooctanoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90201577 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulic acid sulfate levels 33 African ancestry individuals NA Affymetrix [7706872] (imputed) 0 dihydroferulic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801026 GCST90201578 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylcitrulline levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 gamma-glutamylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800690 GCST90201579 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (2) levels 57 African ancestry individuals NA Affymetrix [7551158] (imputed) 0 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90201580 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/14:0, d16:1/15:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201581 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C10H18O2 (7) levels 45 African ancestry individuals NA Affymetrix [7696336] (imputed) 0 glucuronide of C10H18O2 (7) measurement http://www.ebi.ac.uk/efo/EFO_0800652 GCST90201582 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H14O2 (1) levels 57 African ancestry individuals NA Affymetrix [7593036] (imputed) 0 glycine conjugate of C10H14O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800655 GCST90201583 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (1) levels 58 African ancestry individuals NA Affymetrix [7521563] (imputed) 0 glutamine conjugate of C6H10O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800657 GCST90201584 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glyco-beta-muricholate levels 53 African ancestry individuals NA Affymetrix [7687894] (imputed) 0 glyco-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800569 GCST90201585 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,n,n-trimethyl-alanylproline betaine (tmap) levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 N,N,N-trimethyl-alanylproline betaine (TMAP) measurement http://www.ebi.ac.uk/efo/EFO_0800094 GCST90201586 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylhydroxyproline levels 51 African ancestry individuals NA Affymetrix [7774820] (imputed) 0 N-methylhydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800093 GCST90201587 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 8-methoxykynurenate levels 42 African ancestry individuals NA Affymetrix [7716366] (imputed) 0 8-methoxykynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800096 GCST90201588 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienoate (14:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 tetradecadienoate (14:2) measurement http://www.ebi.ac.uk/efo/EFO_0800570 GCST90201589 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-amino-2-piperidone levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90201590 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetoylcarnitine levels 54 African ancestry individuals NA Affymetrix [7683719] (imputed) 0 indoleacetoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800106 GCST90201591 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-isoputreanine levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90201592 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoylcarnitine (C22) levels 47 African ancestry individuals NA Affymetrix [7584566] (imputed) 0 behenoylcarnitine (C22) measurement http://www.ebi.ac.uk/efo/EFO_0800539 GCST90201543 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroylcarnitine (C24) levels 59 African ancestry individuals NA Affymetrix [7490317] (imputed) 0 lignoceroylcarnitine (C24) measurement http://www.ebi.ac.uk/efo/EFO_0800541 GCST90201544 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cerotoylcarnitine (C26) levels 59 African ancestry individuals NA Affymetrix [7486916] (imputed) 0 cerotoylcarnitine (C26) measurement http://www.ebi.ac.uk/efo/EFO_0800542 GCST90201545 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ximenoylcarnitine (C26:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 ximenoylcarnitine (C26:1) measurement http://www.ebi.ac.uk/efo/EFO_0800543 GCST90201546 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nervonoylcarnitine (C24:1) levels 53 African ancestry individuals NA Affymetrix [7793454] (imputed) 0 nervonoylcarnitine (C24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800549 GCST90201547 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoylcarnitine (C20:1) levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 eicosenoylcarnitine (C20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800545 GCST90201548 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:1/20:0, d16:1/22:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycosyl ceramide (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800551 GCST90201549 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 carotene diol (1) measurement http://www.ebi.ac.uk/efo/EFO_0800170 GCST90201550 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethyl alpha-glucopyranoside levels 44 African ancestry individuals NA Affymetrix [7540417] (imputed) 0 ethyl alpha-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801019 GCST90201551 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 carotene diol (2) measurement http://www.ebi.ac.uk/efo/EFO_0800171 GCST90201552 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N,N-trimethyl-5-aminovalerate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90201553 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortolone glucuronide (1) levels 58 African ancestry individuals NA Affymetrix [7525918] (imputed) 0 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90201554 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (N(1) + N(8))-acetylspermidine levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 blood N(1)-acetylspermidine measurement, blood N(8)-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0022204, http://www.ebi.ac.uk/efo/EFO_0022205 GCST90201555 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (3) levels 55 African ancestry individuals NA Affymetrix [7585696] (imputed) 0 carotene diol (3) measurement http://www.ebi.ac.uk/efo/EFO_0800172 GCST90201556 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoleoylcarnitine levels 49 African ancestry individuals NA Affymetrix [7472301] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201557 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-butenoylglycine levels 40 African ancestry individuals NA Affymetrix [7340367] (imputed) 0 2-butenoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800556 GCST90201558 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-2-hexenoylglycine levels 38 African ancestry individuals NA Affymetrix [7345618] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201559 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxy-cmpf levels 58 African ancestry individuals NA Affymetrix [7513149] (imputed) 0 hydroxy-CMPF measurement http://www.ebi.ac.uk/efo/EFO_0800557 GCST90201560 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-dodecenoylcarnitine (C12:1) levels 55 African ancestry individuals NA Affymetrix [7602677] (imputed) 0 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90201561 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-furoylcarnitine levels 40 African ancestry individuals NA Affymetrix [7335270] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201562 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecenedioate (C16:1-DC) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90201563 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioate (C18:1-DC) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 octadecenedioate (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800563 GCST90201564 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyarachidate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-hydroxyarachidate measurement http://www.ebi.ac.uk/efo/EFO_0800558 GCST90201565 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecenedioate (C12:1-DC) levels 59 African ancestry individuals NA Affymetrix [7496533] (imputed) 0 dodecenedioate (C12:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800561 GCST90201566 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecadienedioate (C18:2-DC) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 octadecadienedioate (C18:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800565 GCST90201567 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethyl beta-glucopyranoside levels 57 African ancestry individuals NA Affymetrix [7562313] (imputed) 0 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90201593 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxysebacate levels 55 African ancestry individuals NA Affymetrix [7614088] (imputed) 0 2-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800571 GCST90201594 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,N6-dimethyllysine levels 57 African ancestry individuals NA Affymetrix [7593853] (imputed) 0 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90201595 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 3-sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90201596 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-bromotryptophan levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 6-bromotryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800099 GCST90201597 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Delta-CEHC levels 48 African ancestry individuals NA Affymetrix [7563976] (imputed) 0 delta-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800174 GCST90201598 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N-dimethylalanine levels 59 African ancestry individuals NA Affymetrix [7495043] (imputed) 0 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90201599 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl valine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-carboxyethylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800103 GCST90201600 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecadienoate (12:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 dodecadienoate (12:2) measurement http://www.ebi.ac.uk/efo/EFO_0800572 GCST90201601 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol disulfate levels 72 South Asian ancestry individuals NA Affymetrix [4538117] (imputed) 0 5alpha-androstan-3alpha,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800287 GCST90203316 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholenate sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4392123] (imputed) 0 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90203317 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 21-hydroxypregnenolone disulfate levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90203318 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels 100 South Asian ancestry individuals NA Affymetrix [4528995] (imputed) 0 5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800284 GCST90203319 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 16a-hydroxy DHEA 3-sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90203320 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90203321 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl sphingomyelin (d18:1/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90203322 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels 107 South Asian ancestry individuals NA Affymetrix [4391492] (imputed) 0 Sphingomyelin (d18:1/18:1, d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0022108 GCST90203323 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-beta-alanine levels 107 South Asian ancestry individuals NA Affymetrix [4390341] (imputed) 0 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90203324 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-cholesten-3-one levels 83 South Asian ancestry individuals NA Affymetrix [4442819] (imputed) 0 4-cholesten-3-one measurement http://www.ebi.ac.uk/efo/EFO_0800310 GCST90203325 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tridecenedioate (C13:1-DC) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 tridecenedioate (C13:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800309 GCST90203326 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cinnamoylglycine levels 90 South Asian ancestry individuals NA Affymetrix [4534979] (imputed) 0 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90203327 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ergothioneine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90203328 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 13-HODE + 9-HODE levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 13-HODE + 9-HODE measurement http://www.ebi.ac.uk/efo/EFO_0800308 GCST90203329 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylmethionine levels 94 South Asian ancestry individuals NA Affymetrix [4459010] (imputed) 0 S-methylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800042 GCST90203330 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Andro steroid monosulfate C19H28O6S (1) levels 101 South Asian ancestry individuals NA Affymetrix [4507253] (imputed) 0 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90203331 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenolone sulfate levels 103 South Asian ancestry individuals NA Affymetrix [4472965] (imputed) 0 pregnenolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800303 GCST90203332 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2s,3R-dihydroxybutyrate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2s,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800312 GCST90203333 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoylcarnitine (C10:1) levels 107 South Asian ancestry individuals NA Affymetrix [4392753] (imputed) 0 cis-4-decenoylcarnitine (C10:1) measurement http://www.ebi.ac.uk/efo/EFO_0800311 GCST90203334 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (16 or 17)-methylstearate (a19:0 or i19:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 (16 or 17)-methylstearate (a19:0 or i19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800313 GCST90203335 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4389278] (imputed) 0 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90203336 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydantoin-5-propionate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 hydantoin-5-propionate measurement http://www.ebi.ac.uk/efo/EFO_0800051 GCST90203337 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoursodeoxycholate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 isoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800315 GCST90203338 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyglutamate levels 95 South Asian ancestry individuals NA Affymetrix [4409576] (imputed) 0 4-hydroxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800052 GCST90203339 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2R,3R-dihydroxybutyrate levels 106 South Asian ancestry individuals NA Affymetrix [4410834] (imputed) 0 2R,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800314 GCST90203340 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxy-2-oxoglutaric acid levels 103 South Asian ancestry individuals NA Affymetrix [4473861] (imputed) 0 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90203341 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine levels 106 South Asian ancestry individuals NA Affymetrix [4409368] (imputed) 0 S-methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800054 GCST90203342 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Formiminoglutamate levels 107 South Asian ancestry individuals NA Affymetrix [4392767] (imputed) 0 formiminoglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800050 GCST90203343 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Argininate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 argininate measurement http://www.ebi.ac.uk/efo/EFO_0800055 GCST90203344 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-oxoarginine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90203345 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantoate levels 101 South Asian ancestry individuals NA Affymetrix [4505915] (imputed) 0 blood pantoate measurement http://www.ebi.ac.uk/efo/EFO_0022210 GCST90203346 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone glucuronide levels 100 South Asian ancestry individuals NA Affymetrix [4528468] (imputed) 0 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90203347 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutaramate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 alpha-ketoglutaramate measurement http://www.ebi.ac.uk/efo/EFO_0800046 GCST90203348 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutaconate levels 107 South Asian ancestry individuals NA Affymetrix [4395332] (imputed) 0 3-methylglutaconate measurement http://www.ebi.ac.uk/efo/EFO_0800047 GCST90203349 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxyisovalerate levels 107 South Asian ancestry individuals NA Affymetrix [4396968] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90203350 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-(galactosylhydroxy)-L-lysine levels 82 South Asian ancestry individuals NA Affymetrix [4503465] (imputed) 0 5-(galactosylhydroxy)-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800048 GCST90203351 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine disulfide levels 107 South Asian ancestry individuals NA Affymetrix [4394422] (imputed) 0 cysteinylglycine disulfide measurement http://www.ebi.ac.uk/efo/EFO_0800049 GCST90203352 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-oxo-retinoic acid levels 89 South Asian ancestry individuals NA Affymetrix [4327580] (imputed) 0 blood 4-oxo-retinoic acid measurement http://www.ebi.ac.uk/efo/EFO_0022216 GCST90203353 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-5-imidazoleacetate levels 105 South Asian ancestry individuals NA Affymetrix [4436052] (imputed) 0 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90203354 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-GPE (p-18:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-stearoyl)-GPE (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800335 GCST90203355 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C18:2 levels 107 South Asian ancestry individuals NA Affymetrix [4392753] (imputed) 0 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90203356 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to glutamate ratio 8,213 European ancestry individuals NA Affymetrix [15429360] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200879 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarate (C5-DC) to salicylate ratio 7,684 European ancestry individuals NA Affymetrix [15410464] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200880 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate to N-acetylglucosamine to N-acetylgalactosamine ratio 7,899 European ancestry individuals NA Affymetrix [15416513] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200881 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate to mannose ratio 8,162 European ancestry individuals NA Affymetrix [15427657] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200882 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to acetoacetate ratio 6,791 European ancestry individuals NA Affymetrix [15368126] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200883 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose to N-acetylglucosamine to N-acetylgalactosamine ratio 7,907 European ancestry individuals NA Affymetrix [15416676] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200884 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylpyruvate to citrate ratio 8,177 European ancestry individuals NA Affymetrix [15429018] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200885 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylpyruvate to 4-hydroxyphenylpyruvate ratio 7,829 European ancestry individuals NA Affymetrix [15415896] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200886 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol to cortisol ratio 8,211 European ancestry individuals NA Affymetrix [15429346] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200887 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrate to 4-hydroxyphenylpyruvate ratio 7,851 European ancestry individuals NA Affymetrix [15417294] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200888 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol to taurocholate ratio 7,611 European ancestry individuals NA Affymetrix [15405905] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200889 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphingadienine (d18:2/16:0) levels 57 African ancestry individuals NA Affymetrix [7525187] (imputed) 0 N-palmitoyl-sphingadienine (d18:2/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800516 GCST90201529 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:2/24:1, d18:1/24:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycosyl ceramide (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0800532 GCST90201530 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosatrienoate (22:3n6) levels 32 African ancestry individuals NA Affymetrix [7758236] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201531 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/20:0, d16:0/22:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201532 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/19:0, d19:1/18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201533 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/24:2) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201534 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201535 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/21:0, d16:2/23:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201536 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/23:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201537 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201538 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Heneicosapentaenoate (21:5n3) levels 39 African ancestry individuals NA Affymetrix [7390695] (imputed) 0 heneicosapentaenoate (21:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800537 GCST90201539 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:2/16:0, d18:2/15:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201540 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenoylcarnitine (C18:3) levels 57 African ancestry individuals NA Affymetrix [7534753] (imputed) 0 linolenoylcarnitine (C18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800538 GCST90201541 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidoylcarnitine (C20) levels 56 African ancestry individuals NA Affymetrix [7672459] (imputed) 0 arachidoylcarnitine (C20) measurement http://www.ebi.ac.uk/efo/EFO_0800540 GCST90201542 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyruvate to N-acetylneuraminate ratio 8,194 European ancestry individuals NA Affymetrix [15428996] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200779 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alanine to pyruvate ratio 8,250 European ancestry individuals NA Affymetrix [15430874] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200780 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to maltose ratio 6,308 European ancestry individuals NA Affymetrix [15344203] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200781 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose to trans-4-hydroxyproline ratio 8,194 European ancestry individuals NA Affymetrix [15428740] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200782 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose to S-methylcysteine ratio 8,182 European ancestry individuals NA Affymetrix [15427929] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200783 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate to cysteine ratio 8,199 European ancestry individuals NA Affymetrix [15426850] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200784 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine to 5-oxoproline ratio 8,203 European ancestry individuals NA Affymetrix [15429376] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200785 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine to alanine ratio 8,220 European ancestry individuals NA Affymetrix [15429860] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200786 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine to asparagine ratio 8,251 European ancestry individuals NA Affymetrix [15431170] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200787 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-oxoproline to citrate ratio 8,256 European ancestry individuals NA Affymetrix [15430231] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200788 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-tocopherol to sulfate ratio 8,201 European ancestry individuals NA Affymetrix [15428607] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200789 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thyroxine to taurocholate ratio 7,615 European ancestry individuals NA Affymetrix [15405136] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200790 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatine to carnitine ratio 8,235 European ancestry individuals NA Affymetrix [15430150] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200791 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine to palmitoylcarnitine (C16) ratio 8,146 European ancestry individuals NA Affymetrix [15427190] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200792 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate to glycolithocholate sulfate ratio 7,043 European ancestry individuals NA Affymetrix [15381234] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200793 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl-linoleoyl-glycerol (18:1 to 18:2) [2] to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [1] ratio 7,620 European ancestry individuals NA Affymetrix [15401957] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200794 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl-linoleoyl-glycerol (18:1 to 18:2) [2] to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [2] ratio 7,615 European ancestry individuals NA Affymetrix [15401922] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200795 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to (N(1) + N(8))-acetylspermidine ratio 7,287 European ancestry individuals NA Affymetrix [15387913] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200796 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to N-acetylputrescine ratio 7,299 European ancestry individuals NA Affymetrix [15388943] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200797 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 4-sulfate to dopamine 3-O-sulfate ratio 6,840 European ancestry individuals NA Affymetrix [15367805] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200798 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to adenosine 5'-diphosphate (ADP) ratio 4,195 European ancestry individuals NA Affymetrix [15417882] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200799 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to histidine ratio 7,297 European ancestry individuals NA Affymetrix [15389128] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200800 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methylthioadenosine (MTA) to phosphate ratio 8,261 European ancestry individuals NA Affymetrix [15431001] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200801 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine to pyruvate ratio 8,241 European ancestry individuals NA Affymetrix [15428401] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200802 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to phosphate ratio 7,382 European ancestry individuals NA Affymetrix [15392463] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200803 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (Z,Z) to taurocholate ratio 7,620 European ancestry individuals NA Affymetrix [15406151] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200829 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate to adenosine 3',5'-cyclic monophosphate (cAMP) ratio 6,359 European ancestry individuals NA Affymetrix [15343876] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200830 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate to phosphate ratio 7,742 European ancestry individuals NA Affymetrix [15413743] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200831 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to citrate ratio 4,567 European ancestry individuals NA Affymetrix [15443946] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200832 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate to adenosine 5'-monophosphate (AMP) ratio 7,769 European ancestry individuals NA Affymetrix [15415008] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200833 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to glycerol 3-phosphate ratio 4,588 European ancestry individuals NA Affymetrix [15442233] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200834 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to glycerol ratio 4,575 European ancestry individuals NA Affymetrix [15444251] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200835 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol to glycerol 3-phosphate ratio 8,188 European ancestry individuals NA Affymetrix [15427011] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200836 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to glutamate ratio 4,556 European ancestry individuals NA Affymetrix [15443590] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200837 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to glutamate ratio 8,211 European ancestry individuals NA Affymetrix [15430457] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200838 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to aspartate ratio 4,563 European ancestry individuals NA Affymetrix [15443383] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200839 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to flavin adenine dinucleotide (FAD) ratio 3,441 European ancestry individuals NA Affymetrix [15362845] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200840 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to oxalate (ethanedioate) ratio 4,556 European ancestry individuals NA Affymetrix [15443975] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200841 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrate to oxalate (ethanedioate) ratio 8,097 European ancestry individuals NA Affymetrix [15424311] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200842 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to flavin adenine dinucleotide (FAD) ratio 6,188 European ancestry individuals NA Affymetrix [15335000] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200843 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate to phosphate ratio 8,297 European ancestry individuals NA Affymetrix [15432198] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200844 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to citrate ratio 8,193 European ancestry individuals NA Affymetrix [15429575] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200845 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylalanine to phosphate ratio 8,294 European ancestry individuals NA Affymetrix [15432103] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200846 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to tryptophan ratio 8,206 European ancestry individuals NA Affymetrix [15429839] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200847 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to glutamine ratio 8,196 European ancestry individuals NA Affymetrix [15429366] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200848 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to threonine ratio 8,173 European ancestry individuals NA Affymetrix [15429002] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200849 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to tryptophan ratio 8,180 European ancestry individuals NA Affymetrix [15429221] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200850 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to glycine ratio 8,195 European ancestry individuals NA Affymetrix [15429582] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200851 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to arginine ratio 8,185 European ancestry individuals NA Affymetrix [15429106] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200852 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to tyrosine ratio 8,193 European ancestry individuals NA Affymetrix [15429705] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200853 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to pyruvate ratio 7,296 European ancestry individuals NA Affymetrix [15388521] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200804 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to carnitine ratio 7,338 European ancestry individuals NA Affymetrix [15390709] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200805 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to ergothioneine ratio 7,291 European ancestry individuals NA Affymetrix [15389320] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200806 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine to ergothioneine ratio 8,110 European ancestry individuals NA Affymetrix [15426618] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200807 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to choline ratio 7,295 European ancestry individuals NA Affymetrix [15388902] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200808 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to taurocholate ratio 6,777 European ancestry individuals NA Affymetrix [15362253] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200809 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to kynurenine ratio 8,272 European ancestry individuals NA Affymetrix [15431458] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200810 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Choline to taurocholate ratio 7,625 European ancestry individuals NA Affymetrix [15406479] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200811 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate to kynurenine ratio 8,184 European ancestry individuals NA Affymetrix [15426860] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200812 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ornithine to glutamate ratio 8,202 European ancestry individuals NA Affymetrix [15428262] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200813 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to ornithine ratio 8,273 European ancestry individuals NA Affymetrix [15431492] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200814 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyisobutyrate to adenosine 5'-diphosphate (ADP) ratio 4,488 European ancestry individuals NA Affymetrix [15437474] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200815 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to aspartate ratio 8,272 European ancestry individuals NA Affymetrix [15431441] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200816 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyisobutyrate to phosphate ratio 8,170 European ancestry individuals NA Affymetrix [15427699] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200817 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to glycerate ratio 4,544 European ancestry individuals NA Affymetrix [15443317] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200818 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phosphoglycerate to glycerate ratio 8,101 European ancestry individuals NA Affymetrix [15425320] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200819 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to valine ratio 4,608 European ancestry individuals NA Affymetrix [15445626] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200820 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to glycine ratio 4,577 European ancestry individuals NA Affymetrix [15444772] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200821 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to valine ratio 8,277 European ancestry individuals NA Affymetrix [15431629] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200822 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to N-palmitoyl-sphingosine (d18:1 to 16:0) ratio 4,561 European ancestry individuals NA Affymetrix [15443271] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200823 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to sulfate ratio 4,570 European ancestry individuals NA Affymetrix [15444279] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200824 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to sulfate ratio 8,211 European ancestry individuals NA Affymetrix [15428574] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200825 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine to phosphate ratio 8,271 European ancestry individuals NA Affymetrix [15431669] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200826 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to N-palmitoyl-sphingosine (d18:1 to 16:0) ratio 8,223 European ancestry individuals NA Affymetrix [15430113] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200827 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate to bilirubin (Z,Z) ratio 7,747 European ancestry individuals NA Affymetrix [15414235] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200828 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine to phosphate ratio 8,297 European ancestry individuals NA Affymetrix [15432380] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200854 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to threonine ratio 8,226 European ancestry individuals NA Affymetrix [15430293] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200855 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to glutamine ratio 8,258 European ancestry individuals NA Affymetrix [15431351] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200856 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to aspartate ratio 8,205 European ancestry individuals NA Affymetrix [15429312] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200857 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to tyrosine ratio 8,226 European ancestry individuals NA Affymetrix [15430025] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200858 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to asparagine ratio 8,188 European ancestry individuals NA Affymetrix [15429547] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200859 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to serine ratio 8,194 European ancestry individuals NA Affymetrix [15429478] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200860 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine to phosphate ratio 8,294 European ancestry individuals NA Affymetrix [15432017] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200861 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to methionine ratio 8,194 European ancestry individuals NA Affymetrix [15429544] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200862 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to serine ratio 8,226 European ancestry individuals NA Affymetrix [15428649] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200863 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine to phosphate ratio 8,291 European ancestry individuals NA Affymetrix [15432092] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200864 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to histidine ratio 8,180 European ancestry individuals NA Affymetrix [15429172] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200865 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. phosphate to asparagine ratio 8,249 European ancestry individuals NA Affymetrix [15430935] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200866 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to isoleucine ratio 8,200 European ancestry individuals NA Affymetrix [15429842] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200867 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoleucine to phosphate ratio 8,298 European ancestry individuals NA Affymetrix [15432369] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200868 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to valine ratio 8,225 European ancestry individuals NA Affymetrix [15429772] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200869 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to acetoacetate ratio 6,773 European ancestry individuals NA Affymetrix [15367070] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200870 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to cysteine ratio 8,177 European ancestry individuals NA Affymetrix [15429354] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200871 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to cysteine ratio 8,195 European ancestry individuals NA Affymetrix [15427834] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200872 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisol to 4-cholesten-3-one ratio 7,027 European ancestry individuals NA Affymetrix [15375841] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200873 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine to taurine ratio 8,193 European ancestry individuals NA Affymetrix [15429201] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200874 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine to glutamate ratio 8,197 European ancestry individuals NA Affymetrix [15429837] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200875 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisone to 4-cholesten-3-one ratio 6,971 European ancestry individuals NA Affymetrix [15372915] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200876 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurine to glutamate ratio 8,220 European ancestry individuals NA Affymetrix [15427719] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200877 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarate (C5-DC) to caprylate (8:0) ratio 7,685 European ancestry individuals NA Affymetrix [15409021] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200878 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-ketocaprylate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-ketocaprylate measurement http://www.ebi.ac.uk/efo/EFO_0800110 GCST90203661 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxymethyl-2-furoylcarnitine levels 57 South Asian ancestry individuals NA Affymetrix [4299820] (imputed) 0 5-hydroxymethyl-2-furoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801053 GCST90203662 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800583 GCST90203663 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ethylcatechol sulfate (1) levels 69 South Asian ancestry individuals NA Affymetrix [4299999] (imputed) 0 3-ethylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801047 GCST90203664 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylcatechol sulfate (1) levels 90 South Asian ancestry individuals NA Affymetrix [4529943] (imputed) 0 4-acetylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801049 GCST90203665 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxy-2-methylpyridine sulfate levels 69 South Asian ancestry individuals NA Affymetrix [4309705] (imputed) 0 5-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801051 GCST90203666 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylthreonine levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90201124 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-heptadecenoate (17:1n7) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 10-heptadecenoate 17:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021060 GCST90201125 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-nonadecenoate (19:1n9) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90201126 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylisoleucine levels 53 African ancestry individuals NA Affymetrix [7830139] (imputed) 0 N-acetylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800021 GCST90201127 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octanoylcarnitine (c8) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90201128 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tauro-beta-muricholate levels 42 African ancestry individuals NA Affymetrix [7796710] (imputed) 0 tauro-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800213 GCST90201129 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decanoylcarnitine (C10) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90201130 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylphenylalanine levels 59 African ancestry individuals NA Affymetrix [7517115] (imputed) 0 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90201131 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Campesterol levels 47 African ancestry individuals NA Affymetrix [7634401] (imputed) 0 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90201132 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Piperine levels 59 African ancestry individuals NA Affymetrix [7494771] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90201133 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90201134 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPC (16:0) levels 59 African ancestry individuals NA Affymetrix [7492232] (imputed) 0 1-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800214 GCST90201135 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylasparagine levels 57 African ancestry individuals NA Affymetrix [7540353] (imputed) 0 blood N-acetylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0022206 GCST90201136 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-glutamine levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90201137 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylarginine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90201138 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPC (18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800218 GCST90201139 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-gpc (18:0) levels 59 African ancestry individuals NA Affymetrix [7492232] (imputed) 0 1-stearoyl-GPC (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800217 GCST90201140 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylhistidine levels 53 African ancestry individuals NA Affymetrix [7671836] (imputed) 0 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90201141 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Laurylcarnitine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90201142 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylcitrulline levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 gamma-glutamylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800690 GCST90203611 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H14O2 (1) levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 glycine conjugate of C10H14O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800655 GCST90203612 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-formylindole levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90203613 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/14:0, d16:1/15:0) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203614 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (2) levels 107 South Asian ancestry individuals NA Affymetrix [4390541] (imputed) 0 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90203615 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (1) levels 104 South Asian ancestry individuals NA Affymetrix [4453721] (imputed) 0 glutamine conjugate of C6H10O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800657 GCST90203616 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulic acid sulfate levels 72 South Asian ancestry individuals NA Affymetrix [4507938] (imputed) 0 dihydroferulic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801026 GCST90203617 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H12O2 levels 90 South Asian ancestry individuals NA Affymetrix [4547701] (imputed) 0 glycine conjugate of C10H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800654 GCST90203618 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C7H12O2 levels 102 South Asian ancestry individuals NA Affymetrix [4493086] (imputed) 0 glutamine conjugate of C7H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800656 GCST90203619 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 3-sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4394792] (imputed) 0 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90203620 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 8-methoxykynurenate levels 98 South Asian ancestry individuals NA Affymetrix [4350648] (imputed) 0 8-methoxykynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800096 GCST90203621 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N-dimethylalanine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90203622 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienoate (14:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 tetradecadienoate (14:2) measurement http://www.ebi.ac.uk/efo/EFO_0800570 GCST90203623 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-amino-2-piperidone levels 107 South Asian ancestry individuals NA Affymetrix [4396465] (imputed) 0 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90203624 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxysebacate levels 102 South Asian ancestry individuals NA Affymetrix [4487096] (imputed) 0 2-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800571 GCST90203625 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethyl beta-glucopyranoside levels 107 South Asian ancestry individuals NA Affymetrix [4389201] (imputed) 0 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90203626 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,2'-Methylenebis(6-tert-butyl-p-cresol) levels 96 South Asian ancestry individuals NA Affymetrix [4422610] (imputed) 0 blood 2,2'-Methylenebis(6-tert-butyl-p-cresol) measurement http://www.ebi.ac.uk/efo/EFO_0022208 GCST90203627 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoleglyoxylic acid levels 101 South Asian ancestry individuals NA Affymetrix [4507533] (imputed) 0 3-indoleglyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801027 GCST90203628 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-bromotryptophan levels 107 South Asian ancestry individuals NA Affymetrix [4390292] (imputed) 0 6-bromotryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800099 GCST90203629 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Delta-CEHC levels 71 South Asian ancestry individuals NA Affymetrix [4545228] (imputed) 0 delta-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800174 GCST90203630 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetoylcarnitine levels 98 South Asian ancestry individuals NA Affymetrix [4354306] (imputed) 0 indoleacetoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800106 GCST90203631 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl tyrosine levels 82 South Asian ancestry individuals NA Affymetrix [4528244] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203632 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl valine levels 107 South Asian ancestry individuals NA Affymetrix [4393268] (imputed) 0 1-carboxyethylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800103 GCST90203633 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,N6-dimethyllysine levels 107 South Asian ancestry individuals NA Affymetrix [4392821] (imputed) 0 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90203634 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl leucine levels 98 South Asian ancestry individuals NA Affymetrix [4374509] (imputed) 0 N-acetyl-l-leucine measurement http://www.ebi.ac.uk/efo/EFO_0021653 GCST90203635 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-palmitoleoyl-GPC (16:1) levels 44 African ancestry individuals NA Affymetrix [7734642] (imputed) 0 2-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800240 GCST90201193 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxy-3-methylvalerate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-hydroxy-3-methylvalerate measurement http://www.ebi.ac.uk/efo/EFO_0800027 GCST90201194 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-palmitoyl-GPC (16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800241 GCST90201195 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPE (16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800245 GCST90201196 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcitrulline levels 58 African ancestry individuals NA Affymetrix [7510466] (imputed) 0 N-acetylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800028 GCST90201197 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPE (18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800247 GCST90201198 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonoyl-GPE (20:4n6) levels 59 African ancestry individuals NA Affymetrix [7496336] (imputed) 0 1-arachidonoyl-GPE (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800248 GCST90201199 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxypalmitate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90201200 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate (n6 DPA; 22:5n6) levels 57 African ancestry individuals NA Affymetrix [7529804] (imputed) 0 docosapentaenoate (n6 DPA; 22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800249 GCST90201201 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gulonate levels 53 African ancestry individuals NA Affymetrix [7655428] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90201202 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylglycine levels 56 African ancestry individuals NA Affymetrix [7545535] (imputed) 0 isobutyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800029 GCST90201203 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarylcarnitine (c5-dc) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glutarylcarnitine (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800030 GCST90201204 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroquinone sulfate levels 53 African ancestry individuals NA Affymetrix [7792828] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90201205 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovaleroylcarnitine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 beta-hydroxyisovaleroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800031 GCST90201206 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C5:1 levels 59 African ancestry individuals NA Affymetrix [7499281] (imputed) 0 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90201207 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylglycine levels 35 African ancestry individuals NA Affymetrix [7366010] (imputed) 0 hexanoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800233 GCST90201208 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecanedioate (C14-DC) levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90201209 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioate levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90201210 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecanedioate (C16-DC) levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90201211 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxycaproate levels 48 African ancestry individuals NA Affymetrix [7439468] (imputed) 0 alpha-hydroxycaproate measurement http://www.ebi.ac.uk/efo/EFO_0800261 GCST90201212 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 7-alpha-hydroxy-3-oxo-4-cholestenoate 7-Hoca measurement http://www.ebi.ac.uk/efo/EFO_0021116 GCST90201213 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate sulfate levels 58 African ancestry individuals NA Affymetrix [7549795] (imputed) 0 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90201214 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-ribosyl-imidazoleacetate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90201215 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetylglutamine levels 48 African ancestry individuals NA Affymetrix [7465152] (imputed) 0 indoleacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800035 GCST90201216 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycarnitine levels 58 African ancestry individuals NA Affymetrix [7515709] (imputed) 0 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90201217 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-hydroxyphenyl)propionate levels 50 African ancestry individuals NA Affymetrix [7600964] (imputed) 0 3-(3-hydroxyphenyl)propionate measurement http://www.ebi.ac.uk/efo/EFO_0800952 GCST90201218 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,4-dihydroxybutyrate levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 blood 3,4-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022215 GCST90201219 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurolithocholate 3-sulfate levels 58 African ancestry individuals NA Affymetrix [7549795] (imputed) 0 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90201220 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphoethanolamine levels 59 African ancestry individuals NA Affymetrix [7492232] (imputed) 0 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90201221 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-aspartyl-glutamate (naag) levels 53 African ancestry individuals NA Affymetrix [7689056] (imputed) 0 N-acetyl-aspartyl-glutamate (NAAG) measurement http://www.ebi.ac.uk/efo/EFO_0800033 GCST90201222 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Catechol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90201223 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylglutamine levels 57 African ancestry individuals NA Affymetrix [7559421] (imputed) 0 hexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800262 GCST90201224 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-acetyllysine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90201225 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan betaine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90201226 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenate (20:3n3 or n6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90201227 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPI (16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-GPI (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800257 GCST90201228 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyrraline levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90201229 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethylarginine (sdma + adma) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90201230 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPI (18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-linoleoyl-GPI (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800266 GCST90201231 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylphenol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90201232 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylphenylsulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90201233 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-cresol sulfate levels 51 African ancestry individuals NA Affymetrix [7779427] (imputed) 0 O-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800955 GCST90201234 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylalanine levels 49 African ancestry individuals NA Affymetrix [7387628] (imputed) 0 gamma-glutamylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800675 GCST90201235 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyladipate levels 41 African ancestry individuals NA Affymetrix [7869013] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90201236 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylserine levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90201237 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPI (18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-oleoyl-GPI (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800265 GCST90201238 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thymol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90201239 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,E) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201240 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPE (18:0/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-stearoyl-2-oleoyl-GPE (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800269 GCST90201241 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholenate sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90201242 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,7-dimethyluric acid levels 54 African ancestry individuals NA Affymetrix [7623598] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90201168 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-carbamoylthreonyladenosine levels 58 African ancestry individuals NA Affymetrix [7524129] (imputed) 0 N6-carbamoylthreonyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800629 GCST90201169 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90201170 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyhippurate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90201171 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methyluridine (ribothymidine) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90201172 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-amino-3-carboxypropyl)uridine levels 57 African ancestry individuals NA Affymetrix [7543979] (imputed) 0 3-(3-amino-3-carboxypropyl)uridine measurement http://www.ebi.ac.uk/efo/EFO_0800632 GCST90201173 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5,6-dihydrouridine levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 5,6-dihydrouridine measurement http://www.ebi.ac.uk/efo/EFO_0800631 GCST90201174 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydodecanedioate levels 44 African ancestry individuals NA Affymetrix [7676689] (imputed) 0 3-hydroxydodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0800226 GCST90201175 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotidine levels 55 African ancestry individuals NA Affymetrix [7642531] (imputed) 0 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90201176 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylguanine levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90201177 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonylglycerol (20:4) levels 55 African ancestry individuals NA Affymetrix [7595788] (imputed) 0 1-arachidonylglycerol (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800224 GCST90201178 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerylglycine levels 54 African ancestry individuals NA Affymetrix [7675055] (imputed) 0 isovalerylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800025 GCST90201179 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine-glutathione disulfide levels 53 African ancestry individuals NA Affymetrix [7612403] (imputed) 0 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90201180 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPG (18:0) levels 54 African ancestry individuals NA Affymetrix [7600152] (imputed) 0 1-stearoyl-GPG (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800228 GCST90201181 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPE (18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800227 GCST90201182 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylisoleucine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90201183 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcarnitine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90201184 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyl-2-pyridone-5-carboxamide levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90201185 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylcytidine levels 57 African ancestry individuals NA Affymetrix [7539749] (imputed) 0 3-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800633 GCST90201186 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-2-aminobutyrate levels 56 African ancestry individuals NA Affymetrix [7591779] (imputed) 0 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90201187 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90201188 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoyl-GPC (16:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800231 GCST90201189 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPE (18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800246 GCST90201190 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine degradant levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90201191 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homostachydrine levels 59 African ancestry individuals NA Affymetrix [7496805] (imputed) 0 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90201192 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecadienoate (12:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 dodecadienoate (12:2) measurement http://www.ebi.ac.uk/efo/EFO_0800572 GCST90203636 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl isoleucine levels 101 South Asian ancestry individuals NA Affymetrix [4522994] (imputed) 0 1-carboxyethylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800105 GCST90203637 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl phenylalanine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-carboxyethylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800101 GCST90203638 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-isoputreanine levels 107 South Asian ancestry individuals NA Affymetrix [4392767] (imputed) 0 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90203639 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (3) levels 94 South Asian ancestry individuals NA Affymetrix [4461176] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801031 GCST90203640 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (1) levels 99 South Asian ancestry individuals NA Affymetrix [4362724] (imputed) 0 sulfate of piperine metabolite C18H21NO3 (1) measurement http://www.ebi.ac.uk/efo/EFO_0801036 GCST90203641 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (5) levels 92 South Asian ancestry individuals NA Affymetrix [4502952] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (5) measurement http://www.ebi.ac.uk/efo/EFO_0801033 GCST90203642 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (2) levels 105 South Asian ancestry individuals NA Affymetrix [4436527] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90203643 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (4) levels 105 South Asian ancestry individuals NA Affymetrix [4429880] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90203644 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (3) levels 102 South Asian ancestry individuals NA Affymetrix [4502950] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90203645 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylcatechol sulfate levels 105 South Asian ancestry individuals NA Affymetrix [4426755] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90203646 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (3) levels 96 South Asian ancestry individuals NA Affymetrix [4427314] (imputed) 0 sulfate of piperine metabolite C18H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801037 GCST90203647 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-naphthol sulfate levels 103 South Asian ancestry individuals NA Affymetrix [4459152] (imputed) 0 2-naphthol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801038 GCST90203648 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyandrosterone glucuronide levels 103 South Asian ancestry individuals NA Affymetrix [4462156] (imputed) 0 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90203649 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl vanillate sulfate levels 56 South Asian ancestry individuals NA Affymetrix [4364937] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203650 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6,N6-dimethyllysine levels 99 South Asian ancestry individuals NA Affymetrix [4334838] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203651 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylcatechol sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4390947] (imputed) 0 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90203652 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid glucuronide levels 105 South Asian ancestry individuals NA Affymetrix [4437127] (imputed) 0 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90203653 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyetiocholanolone glucuronide levels 70 South Asian ancestry individuals NA Affymetrix [4584726] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203654 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6-methyllysine levels 101 South Asian ancestry individuals NA Affymetrix [4508751] (imputed) 0 N2-acetyl,N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800109 GCST90203655 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lithocholate sulfate (1) levels 83 South Asian ancestry individuals NA Affymetrix [4482375] (imputed) 0 lithocholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800579 GCST90203656 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylhexanoylglutamine levels 63 South Asian ancestry individuals NA Affymetrix [4485685] (imputed) 0 4-methylhexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800576 GCST90203657 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoylcarnitine (1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-hydroxyhexanoylcarnitine (1) measurement http://www.ebi.ac.uk/efo/EFO_0800580 GCST90203658 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholic acid sulfate (1) levels 93 South Asian ancestry individuals NA Affymetrix [4473611] (imputed) 0 glycoursodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800578 GCST90203659 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydrocaffeate sulfate (2) levels 81 South Asian ancestry individuals NA Affymetrix [4512697] (imputed) 0 dihydrocaffeate sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801044 GCST90203660 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcarnitine levels 58 African ancestry individuals NA Affymetrix [7502770] (imputed) 0 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90201143 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoate (20:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 eicosenoate (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800220 GCST90201144 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aconitate [cis or trans] levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90201145 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenate [alpha or gamma; (18:3n3 or 6)] levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90201146 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxyisovalerate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90201147 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltryptophan levels 57 African ancestry individuals NA Affymetrix [7548028] (imputed) 0 gamma-glutamyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800671 GCST90201148 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglycine levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90201149 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylmethionine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90201150 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylproline levels 48 African ancestry individuals NA Affymetrix [7468642] (imputed) 0 blood N-acetylproline measurement http://www.ebi.ac.uk/efo/EFO_0022207 GCST90201151 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stachydrine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90201152 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylthreonine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90201153 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythronate levels 59 African ancestry individuals NA Affymetrix [7486916] (imputed) 0 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90201154 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylxanthine levels 49 African ancestry individuals NA Affymetrix [7432447] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90201155 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-gpc (18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800223 GCST90201156 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3,7-trimethylurate levels 45 African ancestry individuals NA Affymetrix [7471939] (imputed) 0 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90201157 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerylcarnitine (C5) levels 59 African ancestry individuals NA Affymetrix [7495043] (imputed) 0 isovalerylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800024 GCST90201158 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol sulfate levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90201159 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolebutyrate levels 31 African ancestry individuals NA Affymetrix [7601068] (imputed) 0 3-Indolebutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021559 GCST90201160 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-formylamino-3-methyluracil levels 40 African ancestry individuals NA Affymetrix [7225802] (imputed) 0 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90201161 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-amino-3-methyluracil levels 54 African ancestry individuals NA Affymetrix [7627227] (imputed) 0 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90201162 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,n2-dimethylguanosine levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90201163 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylxanthine levels 53 African ancestry individuals NA Affymetrix [7652906] (imputed) 0 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90201164 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,7-dimethylurate levels 38 African ancestry individuals NA Affymetrix [7432513] (imputed) 0 3,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800949 GCST90201165 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N4-acetylcytidine levels 47 African ancestry individuals NA Affymetrix [7555451] (imputed) 0 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90201166 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N1-methylinosine levels 58 African ancestry individuals NA Affymetrix [7521834] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90201167 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholenate sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90201243 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23665 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-23665 measurement http://www.ebi.ac.uk/efo/EFO_0800859 GCST90201989 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21845 levels 35 African ancestry individuals NA Affymetrix [7359568] (imputed) 0 X-21845 measurement http://www.ebi.ac.uk/efo/EFO_0800836 GCST90201990 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23659 levels 59 African ancestry individuals NA Affymetrix [7491837] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201991 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23276 levels 44 African ancestry individuals NA Affymetrix [7703528] (imputed) 0 X-23276 measurement http://www.ebi.ac.uk/efo/EFO_0800847 GCST90201992 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23593 levels 57 African ancestry individuals NA Affymetrix [7549773] (imputed) 0 X-23593 measurement http://www.ebi.ac.uk/efo/EFO_0800851 GCST90201993 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22834 levels 44 African ancestry individuals NA Affymetrix [7555143] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201994 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22162 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90201995 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22520 levels 33 African ancestry individuals NA Affymetrix [7615785] (imputed) 0 X-22520 measurement http://www.ebi.ac.uk/efo/EFO_0800843 GCST90201996 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23641 levels 47 African ancestry individuals NA Affymetrix [7682838] (imputed) 0 X-23641 measurement http://www.ebi.ac.uk/efo/EFO_0800854 GCST90201997 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23639 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90201998 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23644 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-23644 measurement http://www.ebi.ac.uk/efo/EFO_0800855 GCST90201999 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22771 levels 58 African ancestry individuals NA Affymetrix [7572138] (imputed) 0 X-22771 measurement http://www.ebi.ac.uk/efo/EFO_0800844 GCST90202000 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22776 levels 53 African ancestry individuals NA Affymetrix [7727500] (imputed) 0 X-22776 measurement http://www.ebi.ac.uk/efo/EFO_0800845 GCST90202001 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23678 levels 33 African ancestry individuals NA Affymetrix [7905447] (imputed) 0 X-23678 measurement http://www.ebi.ac.uk/efo/EFO_0800861 GCST90202002 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23636 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-23636 measurement http://www.ebi.ac.uk/efo/EFO_0800852 GCST90202003 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23648 levels 51 African ancestry individuals NA Affymetrix [7825982] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202004 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23654 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202005 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23782 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-23782 measurement http://www.ebi.ac.uk/efo/EFO_0800865 GCST90202006 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24306 levels 59 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-24306 measurement http://www.ebi.ac.uk/efo/EFO_0800870 GCST90202007 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23739 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90202008 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23780 levels 54 African ancestry individuals NA Affymetrix [7671177] (imputed) 0 X-23780 measurement http://www.ebi.ac.uk/efo/EFO_0800864 GCST90202009 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24337 levels 59 African ancestry individuals NA Affymetrix [7499364] (imputed) 0 X-24337 measurement http://www.ebi.ac.uk/efo/EFO_0800875 GCST90202010 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24518 levels 46 African ancestry individuals NA Affymetrix [7520122] (imputed) 0 X-24518 measurement http://www.ebi.ac.uk/efo/EFO_0800890 GCST90202011 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24307 levels 59 African ancestry individuals NA Affymetrix [7498842] (imputed) 0 X-24307 measurement http://www.ebi.ac.uk/efo/EFO_0800871 GCST90202012 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24295 levels 58 African ancestry individuals NA Affymetrix [7514264] (imputed) 0 X-24295 measurement http://www.ebi.ac.uk/efo/EFO_0800869 GCST90202013 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24456 levels 48 African ancestry individuals NA Affymetrix [7553797] (imputed) 0 X-24456 measurement http://www.ebi.ac.uk/efo/EFO_0800885 GCST90202014 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24334 levels 54 African ancestry individuals NA Affymetrix [7656643] (imputed) 0 X-24334 measurement http://www.ebi.ac.uk/efo/EFO_0800874 GCST90202015 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24241 levels 58 African ancestry individuals NA Affymetrix [7517014] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202016 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24328 levels 58 African ancestry individuals NA Affymetrix [7517884] (imputed) 0 X-24328 measurement http://www.ebi.ac.uk/efo/EFO_0800873 GCST90202017 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24494 levels 48 African ancestry individuals NA Affymetrix [7536709] (imputed) 0 X-24494 measurement http://www.ebi.ac.uk/efo/EFO_0800889 GCST90202018 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24546 levels 54 African ancestry individuals NA Affymetrix [7694915] (imputed) 0 X-24546 measurement http://www.ebi.ac.uk/efo/EFO_0800893 GCST90202019 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24544 levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 X-24544 measurement http://www.ebi.ac.uk/efo/EFO_0800892 GCST90202020 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24531 levels 44 African ancestry individuals NA Affymetrix [7605706] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202021 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24418 levels 38 African ancestry individuals NA Affymetrix [7652675] (imputed) 0 X-24418 measurement http://www.ebi.ac.uk/efo/EFO_0800879 GCST90202022 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23997 levels 57 African ancestry individuals NA Affymetrix [7623697] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90202023 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24556 levels 58 African ancestry individuals NA Affymetrix [7596400] (imputed) 0 X-24556 measurement http://www.ebi.ac.uk/efo/EFO_0800895 GCST90202024 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23974 levels 58 African ancestry individuals NA Affymetrix [7523612] (imputed) 0 X-23974 measurement http://www.ebi.ac.uk/efo/EFO_0800867 GCST90202025 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24736 levels 33 African ancestry individuals NA Affymetrix [7448780] (imputed) 0 X-24736 measurement http://www.ebi.ac.uk/efo/EFO_0800904 GCST90202026 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24757 levels 45 African ancestry individuals NA Affymetrix [7566063] (imputed) 0 X-24757 measurement http://www.ebi.ac.uk/efo/EFO_0800905 GCST90202027 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24801 levels 59 African ancestry individuals NA Affymetrix [7496750] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202028 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24585 levels 59 African ancestry individuals NA Affymetrix [7497538] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202029 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24970 levels 59 African ancestry individuals NA Affymetrix [7496582] (imputed) 0 X-24970 measurement http://www.ebi.ac.uk/efo/EFO_0800913 GCST90202030 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25109 levels 57 African ancestry individuals NA Affymetrix [7634514] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202031 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24588 levels 59 African ancestry individuals NA Affymetrix [7546954] (imputed) 0 X-24588 measurement http://www.ebi.ac.uk/efo/EFO_0800898 GCST90202032 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25419 levels 57 African ancestry individuals NA Affymetrix [7601534] (imputed) 0 X-25419 measurement http://www.ebi.ac.uk/efo/EFO_0800925 GCST90202033 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25172 levels 59 African ancestry individuals NA Affymetrix [7488130] (imputed) 0 X-25172 measurement http://www.ebi.ac.uk/efo/EFO_0800916 GCST90202034 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25420 levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 X-25420 measurement http://www.ebi.ac.uk/efo/EFO_0800926 GCST90202035 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25271 levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 X-25271 measurement http://www.ebi.ac.uk/efo/EFO_0800920 GCST90202036 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25371 levels 58 African ancestry individuals NA Affymetrix [7512499] (imputed) 0 X-25371 measurement http://www.ebi.ac.uk/efo/EFO_0800923 GCST90202037 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6661) (1-(8-5-ladderane-octanyl)-2-(8-3-ladderane-octanyl)-sn-glycerol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of dialkylglycerol in blood serum http://purl.obolibrary.org/obo/OBA_2045052 GCST90280637 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6664) (GW 6471) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 GW 6471 measurement http://www.ebi.ac.uk/efo/EFO_0803499 GCST90280638 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6707) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280639 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6711) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280640 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6712) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280641 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6715) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280642 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6722) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280643 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6726) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280644 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_673) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280645 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6733) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280646 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6734) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280647 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6745) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280648 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6746) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280649 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6747) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280650 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6754) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280651 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6758) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280652 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6760) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280653 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6764) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280654 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6771) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280655 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6776) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 16 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280656 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6781) (1-(8-3-ladderane-octanoyl-2-(8-3-ladderane-octanyl)-sn-glycerol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of 1-(8-[3]-ladderane-octanoyl)-2-(8-[3]-ladderane-octanyl)-sn-glycerol in blood serum http://purl.obolibrary.org/obo/OBA_2045038 GCST90280657 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6784) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280658 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6785) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280659 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6795) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280660 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6796) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 23 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280661 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6064) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280537 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6067) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280538 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6076) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280539 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6079) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280540 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_608) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280541 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6090) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280542 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_61) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280543 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_610) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280544 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6112) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280545 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6126) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280546 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6127) (Quinidine barbiturate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 quinidine barbiturate measurement http://www.ebi.ac.uk/efo/EFO_0803452 GCST90280547 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6133) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280548 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_614) (3-(Phosphoacetylamido)-L-alanine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 3-(phosphoacetylamido)-L-alanine measurement http://www.ebi.ac.uk/efo/EFO_0803475 GCST90280549 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6147) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280550 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6157) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280551 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_616) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280552 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6164) (3-O-(beta-D-glucopyranosyl)-campest-5-en-3beta-ol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of campesterol 3-beta-D-glucoside in blood serum http://purl.obolibrary.org/obo/OBA_2045039 GCST90280553 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6167) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280554 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6173) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280555 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6178) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280556 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_618) (Tromethamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280557 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_619) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280558 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6190) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280559 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6224) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280560 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6227) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 15 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280561 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6487) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280612 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6495) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280613 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6499) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280614 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6505) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280615 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6515) (1-(1Z-eicosenyl)-glycero-3-phospho-(1-myo-inositol)) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 level of 1-O-(1Z-eicosenyl)-sn-glycero-3-phospho-1D-myo-inositol in blood serum http://purl.obolibrary.org/obo/OBA_2045060 GCST90280616 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6516) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280617 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6517) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280618 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6529) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280619 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6542) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280620 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6544) (3-Vinylbacteriochlorophyllide a) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280621 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6546) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280622 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_656) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280623 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6562) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280624 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6568) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280625 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_657) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280626 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6570) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280627 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6575) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280628 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6582) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280629 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6583) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280630 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6593) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280631 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6605) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280632 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6630) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280633 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6635) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280634 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6637) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280635 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6643) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280636 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6361) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280587 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6363) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280588 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_637) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280589 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6379) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280590 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6385) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280591 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6389) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280592 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_639) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280593 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6390) (L-Urobilin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 L-urobilin measurement http://www.ebi.ac.uk/efo/EFO_0800161 GCST90280594 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6396) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280595 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6402) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280596 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_641) (Santene) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 santene measurement http://www.ebi.ac.uk/efo/EFO_0803454 GCST90280597 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6413) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280598 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6416) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280599 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6419) (N-(3E-hexadecenoyl)-deoxysphing-4-enine-1-sulfonate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of N-(3E-hexadecenoyl)-deoxysphing-4-enine-1-sulfonate in blood serum http://purl.obolibrary.org/obo/OBA_2045043 GCST90280600 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6424) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280601 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6432) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280602 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6435) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280603 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6440) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280604 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6446) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280605 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_645) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280606 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6461) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280607 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6465) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280608 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6466) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280609 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6469) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280610 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_648) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280611 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5946) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280512 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5949) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280513 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5950) (3-keto Fusidic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 3-keto fusidic acid measurement http://www.ebi.ac.uk/efo/EFO_0803389 GCST90280514 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5953) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280515 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5958) (1-(10Z13Z16Z-nonadecatrienoyl)-sn-glycero-3-phosphocholine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 level of PC(19:3(10Z,13Z,16Z)/0:0) in blood serum http://purl.obolibrary.org/obo/OBA_2045046 GCST90280516 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5959) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280517 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5962) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280518 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5967) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280519 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5971) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280520 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5972) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280521 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5973) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280522 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5985) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280523 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5987) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280524 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5989) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280525 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5991) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280526 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5993) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280527 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_601) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280528 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6010) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280529 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6012) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280530 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6018) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280531 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_602) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280532 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6021) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280533 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6044) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280534 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6052) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280535 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6057) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280536 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_624) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280562 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6242) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280563 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6249) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280564 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6251) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280565 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6261) (Atractyloside I) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 atractyloside I measurement http://www.ebi.ac.uk/efo/EFO_0803484 GCST90280566 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6262) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280567 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6264) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280568 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6267) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280569 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6275) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280570 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6299) (Biliverdin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90280571 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6313) (Bilirubin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 25 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90280572 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6319) (4E15Z-Bilirubin IXa) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 16 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280573 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6325) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280574 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6328) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280575 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_633) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280576 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6330) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280577 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6332) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280578 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6336) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280579 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6340) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280580 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6341) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280581 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6346) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280582 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6350) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280583 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6352) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280584 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6359) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280585 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6360) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280586 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5782) (2-Apo-beta-carotenal) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280487 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5802) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280488 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5806) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280489 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5817) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280490 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5818) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280491 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5825) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280492 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5834) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280493 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5838) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280494 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5839) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280495 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5854) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280496 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5861) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280497 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5863) (Hodgkinsine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 hodgkinsine measurement http://www.ebi.ac.uk/efo/EFO_0803500 GCST90280498 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5867) (LysoPC(18:2(9Z12Z))) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280499 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5875) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280500 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5878) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280501 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_588) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280502 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5882) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280503 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5889) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280504 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_589) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280505 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5890) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280506 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5891) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280507 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5902) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280508 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5912) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280509 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5920) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280510 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5944) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280511 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5649) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280462 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5653) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280463 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5672) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 16 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280464 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_568) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280465 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5683) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280466 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5690) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280467 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5696) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280468 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5699) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280469 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_570) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280470 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5708) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280471 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5709) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280472 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5715) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280473 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_572) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280474 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5722) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280475 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5734) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280476 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5737) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280477 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5739) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280478 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_574) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280479 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5743) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280480 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5748) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280481 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5751) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280482 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5753) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280483 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5755) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280484 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5766) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280485 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5778) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280486 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6797) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280662 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6802) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280663 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6804) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280664 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6805) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280665 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6820) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280666 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6826) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280667 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6830) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280668 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6835) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280669 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6837) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280670 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6846) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280671 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6847) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280672 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6855) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280673 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6857) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280674 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6859) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280675 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6864) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280676 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6870) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280677 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6874) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280678 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6875) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280679 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6884) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280680 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6891) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280681 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6895) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280682 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6900) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280683 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6904) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280684 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6907) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280685 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6923) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280686 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,N5-diacetylornithine levels 7,596 European ancestry individuals NA Affymetrix [15404884] (imputed) 1 N2,N5-diacetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800070 GCST90199954 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ferulic acid 4-sulfate levels 7,332 European ancestry individuals NA Affymetrix [15394111] (imputed) 1 ferulic acid 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800989 GCST90199955 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1H-indole-7-acetic acid levels 5,986 European ancestry individuals NA Affymetrix [15307250] (imputed) 0 blood 1H-indole-7-acetic acid measurement http://www.ebi.ac.uk/efo/EFO_0022218 GCST90199956 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-hydroxyphenyl)propionate sulfate levels 5,773 European ancestry individuals NA Affymetrix [15309763] (imputed) 0 3-(3-hydroxyphenyl)propionate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800990 GCST90199957 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linolenoyl-GPC (18:3) levels 8,261 European ancestry individuals NA Affymetrix [15431054] (imputed) 0 1-linolenoyl-GPC (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800354 GCST90199958 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-sulfo-l-tyrosine levels 8,229 European ancestry individuals NA Affymetrix [15430195] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90199959 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylanthranilic acid levels 7,534 European ancestry individuals NA Affymetrix [15399447] (imputed) 2 N-formylanthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0800069 GCST90199960 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfone levels 8,254 European ancestry individuals NA Affymetrix [15431252] (imputed) 7 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90199961 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acisoga levels 7,489 European ancestry individuals NA Affymetrix [15404915] (imputed) 5 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90199962 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 17alpha-hydroxypregnanolone glucuronide levels 5,582 European ancestry individuals NA Affymetrix [15290772] (imputed) 1 17alpha-hydroxypregnanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800363 GCST90199963 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Etiocholanolone glucuronide levels 7,821 European ancestry individuals NA Affymetrix [15414026] (imputed) 5 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90199964 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructosyllysine levels 8,238 European ancestry individuals NA Affymetrix [15431064] (imputed) 0 fructosyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800073 GCST90199965 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-oleoyl)-GPE (p-18:1) levels 8,157 European ancestry individuals NA Affymetrix [15427549] (imputed) 0 1-(1-enyl-oleoyl)-GPE (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800359 GCST90199966 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltaurine levels 8,160 European ancestry individuals NA Affymetrix [15427429] (imputed) 3 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90199967 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPG (16:0) levels 7,708 European ancestry individuals NA Affymetrix [15409398] (imputed) 2 1-palmitoyl-GPG (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800367 GCST90199968 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPG (18:1) levels 6,990 European ancestry individuals NA Affymetrix [15375966] (imputed) 2 1-oleoyl-GPG (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800366 GCST90199969 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioylcarnitine (C18:1-DC) levels 8,245 European ancestry individuals NA Affymetrix [15430827] (imputed) 3 octadecenedioylcarnitine (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800370 GCST90199970 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutarylcarnitine (2) levels 8,220 European ancestry individuals NA Affymetrix [15430292] (imputed) 8 3-methylglutarylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800074 GCST90199971 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels 8,267 European ancestry individuals NA Affymetrix [15431708] (imputed) 0 Sphingomyelin (d18:1/24:1, d18:2/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0022113 GCST90199972 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl glucopyranoside (alpha + beta) levels 7,973 European ancestry individuals NA Affymetrix [15418296] (imputed) 1 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90199973 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9-hydroxystearate levels 7,474 European ancestry individuals NA Affymetrix [15401244] (imputed) 0 9-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0800369 GCST90199974 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/14:0, d18:1/14:1) levels 8,278 European ancestry individuals NA Affymetrix [15430038] (imputed) 1 Sphingomyelin (d18:2/14:0, d18:1/14:1) measurement http://www.ebi.ac.uk/efo/EFO_0022114 GCST90199975 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-dihomo-linolenylglycerol (20:3) levels 6,470 European ancestry individuals NA Affymetrix [15353404] (imputed) 0 1-dihomo-linolenylglycerol (20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800374 GCST90199976 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxychlorothalonil levels 8,216 European ancestry individuals NA Affymetrix [15430251] (imputed) 2 4-hydroxychlorothalonil measurement http://www.ebi.ac.uk/efo/EFO_0800992 GCST90199977 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillactate levels 7,935 European ancestry individuals NA Affymetrix [15419383] (imputed) 1 vanillactate measurement http://www.ebi.ac.uk/efo/EFO_0800078 GCST90199978 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl ethanolamide levels 7,214 European ancestry individuals NA Affymetrix [15387034] (imputed) 1 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90200029 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dilinoleoyl-GPC (18:2/18:2) levels 8,227 European ancestry individuals NA Affymetrix [15429706] (imputed) 1 1,2-dilinoleoyl-GPC (18:2/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800388 GCST90200030 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonanoylcarnitine (C9) levels 7,669 European ancestry individuals NA Affymetrix [15404847] (imputed) 3 nonanoylcarnitine (C9) measurement http://www.ebi.ac.uk/efo/EFO_0800381 GCST90200031 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxybutyrate/2-hydroxyisobutyrate levels 8,215 European ancestry individuals NA Affymetrix [15429552] (imputed) 0 2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010979 GCST90200032 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) levels 8,272 European ancestry individuals NA Affymetrix [15431560] (imputed) 2 Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022116 GCST90200033 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tricosanoyl sphingomyelin (d18:1/23:0) levels 8,257 European ancestry individuals NA Affymetrix [15431194] (imputed) 0 tricosanoyl sphingomyelin (d18:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0800401 GCST90200034 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels 8,269 European ancestry individuals NA Affymetrix [15431483] (imputed) 1 palmitoyl dihydrosphingomyelin (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800400 GCST90200035 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoylglycerol (16:1) levels 6,432 European ancestry individuals NA Affymetrix [15349947] (imputed) 0 1-palmitoleoylglycerol (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800398 GCST90200036 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-gpc (18:0/18:2) levels 8,231 European ancestry individuals NA Affymetrix [15430318] (imputed) 2 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90200037 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) levels 8,276 European ancestry individuals NA Affymetrix [15431403] (imputed) 0 1-palmitoyl-2-palmitoleoyl-GPC(16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800406 GCST90200038 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) levels 8,241 European ancestry individuals NA Affymetrix [15429878] (imputed) 6 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800402 GCST90200039 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels 8,273 European ancestry individuals NA Affymetrix [15431628] (imputed) 0 Sphingomyelin (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0022117 GCST90200040 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 8,271 European ancestry individuals NA Affymetrix [15431169] (imputed) 3 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90200041 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleate/vaccenate (18:1) levels 8,230 European ancestry individuals NA Affymetrix [15430410] (imputed) 0 vaccenate (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800397 GCST90200042 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-docosahexaenoyl-gpc (16:0/22:6) levels 8,256 European ancestry individuals NA Affymetrix [15431316] (imputed) 3 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800391 GCST90200043 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-oleoyl-GPE (p-18:0/18:1) levels 8,258 European ancestry individuals NA Affymetrix [15430076] (imputed) 1 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800395 GCST90200044 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels 8,259 European ancestry individuals NA Affymetrix [15431025] (imputed) 7 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800403 GCST90200045 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-gpc (18:0/22:6) levels 8,257 European ancestry individuals NA Affymetrix [15431524] (imputed) 2 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800392 GCST90200046 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels 8,252 European ancestry individuals NA Affymetrix [15430376] (imputed) 1 Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022107 GCST90200047 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (p-16:0/20:4) levels 8,262 European ancestry individuals NA Affymetrix [15431453] (imputed) 1 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800417 GCST90200048 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristoyl dihydrosphingomyelin (d18:0/14:0) levels 8,254 European ancestry individuals NA Affymetrix [15429009] (imputed) 1 myristoyl dihydrosphingomyelin (d18:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800433 GCST90200049 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyindole sulfate levels 6,163 European ancestry individuals NA Affymetrix [15329137] (imputed) 1 5-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800085 GCST90200050 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) levels 8,230 European ancestry individuals NA Affymetrix [15430256] (imputed) 3 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800407 GCST90200051 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels 8,251 European ancestry individuals NA Affymetrix [15430672] (imputed) 3 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90200052 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) levels 8,242 European ancestry individuals NA Affymetrix [15430595] (imputed) 2 Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0022111 GCST90200053 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-carbamoylalanine levels 7,315 European ancestry individuals NA Affymetrix [15394286] (imputed) 0 blood N-carbamoylalanine measurement http://www.ebi.ac.uk/efo/EFO_0022203 GCST90200004 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citraconate/glutaconate levels 8,263 European ancestry individuals NA Affymetrix [15431001] (imputed) 0 blood glutaconic acid measurement, blood Citraconic acid measurement http://www.ebi.ac.uk/efo/EFO_0022200, http://www.ebi.ac.uk/efo/EFO_0022201 GCST90200005 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2,3-benzenetriol sulfate (2) levels 7,484 European ancestry individuals NA Affymetrix [15402971] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90200006 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxycatechol sulfate (2) levels 7,286 European ancestry individuals NA Affymetrix [15388009] (imputed) 0 3-methoxycatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801010 GCST90200007 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. C-glycosyltryptophan levels 8,204 European ancestry individuals NA Affymetrix [15429210] (imputed) 1 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90200008 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxycatechol sulfate (1) levels 8,194 European ancestry individuals NA Affymetrix [15428582] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90200009 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels 8,246 European ancestry individuals NA Affymetrix [15430938] (imputed) 2 Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022112 GCST90200010 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabitol/xylitol levels 8,219 European ancestry individuals NA Affymetrix [15430375] (imputed) 1 arabitol measurement http://www.ebi.ac.uk/efo/EFO_0800148 GCST90200011 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoate levels 8,268 European ancestry individuals NA Affymetrix [15431449] (imputed) 2 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90200012 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:2, d18:2/22:1, d16:1/24:2) levels 8,267 European ancestry individuals NA Affymetrix [15429958] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200013 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3beta-hydroxy-5-cholestenoate levels 8,259 European ancestry individuals NA Affymetrix [15430844] (imputed) 3 3beta-hydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800379 GCST90200014 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylkynurenine (2) levels 6,193 European ancestry individuals NA Affymetrix [15336781] (imputed) 5 N-acetylkynurenine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800083 GCST90200015 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 4-sulfate levels 6,888 European ancestry individuals NA Affymetrix [15369218] (imputed) 0 dopamine 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800081 GCST90200016 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/16:0, d18:1/15:0, d16:1/17:0) levels 8,261 European ancestry individuals NA Affymetrix [15431258] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200017 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adipoylcarnitine (C6-DC) levels 8,216 European ancestry individuals NA Affymetrix [15429676] (imputed) 5 adipoylcarnitine (C6-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800380 GCST90200018 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 3-o-sulfate levels 8,252 European ancestry individuals NA Affymetrix [15430594] (imputed) 0 dopamine 3-O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800082 GCST90200019 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroyl sphingomyelin (d18:1/24:0) levels 8,250 European ancestry individuals NA Affymetrix [15430515] (imputed) 0 lignoceroyl sphingomyelin (d18:1/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800377 GCST90200020 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosamine/n-acetylgalactosamine levels 7,940 European ancestry individuals NA Affymetrix [15418535] (imputed) 2 N-acetylgalactosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149 GCST90200021 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate 3-sulfate levels 8,123 European ancestry individuals NA Affymetrix [15426716] (imputed) 7 glycochenodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800384 GCST90200022 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans 3,4-methyleneheptanoate levels 7,104 European ancestry individuals NA Affymetrix [15377766] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90200023 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurodeoxycholic acid 3-sulfate levels 7,333 European ancestry individuals NA Affymetrix [15392995] (imputed) 4 taurodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800386 GCST90200024 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol glucuronide levels 4,466 European ancestry individuals NA Affymetrix [15440006] (imputed) 0 phenol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800084 GCST90200025 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycodeoxycholate 3-sulfate levels 8,066 European ancestry individuals NA Affymetrix [15424550] (imputed) 4 glycodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800385 GCST90200026 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetoylcarnitine levels 7,523 European ancestry individuals NA Affymetrix [15401033] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200027 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-gpc (18:0/18:1) levels 8,257 European ancestry individuals NA Affymetrix [15431210] (imputed) 1 1-stearoyl-2-oleoyl-GPC (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800389 GCST90200028 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14:1 levels 8,257 European ancestry individuals NA Affymetrix [15431078] (imputed) 0 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90199979 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylphenylalanine levels 7,229 European ancestry individuals NA Affymetrix [15387736] (imputed) 0 N-formylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800075 GCST90199980 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-acetamidophenol sulfate levels 6,984 European ancestry individuals NA Affymetrix [15377656] (imputed) 0 2-acetamidophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801001 GCST90199981 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylguaiacol sulfate levels 7,592 European ancestry individuals NA Affymetrix [15405634] (imputed) 0 4-vinylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800998 GCST90199982 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels 5,920 European ancestry individuals NA Affymetrix [15317561] (imputed) 1 5alpha-androstan-3alpha,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800372 GCST90199983 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic alcohol sulfate levels 5,076 European ancestry individuals NA Affymetrix [15243539] (imputed) 0 blood vanillic alcohol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022214 GCST90199984 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl-4-hydroxybenzoate sulfate levels 8,285 European ancestry individuals NA Affymetrix [15431843] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90199985 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eugenol sulfate levels 7,063 European ancestry individuals NA Affymetrix [15381589] (imputed) 0 eugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800999 GCST90199986 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyresorcinol sulfate levels 5,897 European ancestry individuals NA Affymetrix [15304257] (imputed) 0 2-methoxyresorcinol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801000 GCST90199987 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyramine O-sulfate levels 7,254 European ancestry individuals NA Affymetrix [15392599] (imputed) 0 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90199988 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylguaiacol sulfate levels 7,141 European ancestry individuals NA Affymetrix [15383146] (imputed) 0 4-methylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800996 GCST90199989 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxypyridine sulfate levels 8,270 European ancestry individuals NA Affymetrix [15429916] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90199990 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabonate/xylonate levels 8,211 European ancestry individuals NA Affymetrix [15428906] (imputed) 1 arabonate measurement http://www.ebi.ac.uk/efo/EFO_0801066 GCST90199991 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioylcarnitine (C18-DC) levels 8,049 European ancestry individuals NA Affymetrix [15419517] (imputed) 6 octadecanedioylcarnitine (C18-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800371 GCST90199992 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylcarnitine levels 8,127 European ancestry individuals NA Affymetrix [15427459] (imputed) 2 phenylacetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800686 GCST90199993 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylparaben sulfate levels 6,408 European ancestry individuals NA Affymetrix [15351954] (imputed) 0 blood ethylparaben sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022209 GCST90199994 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:2, d18:2/20:1, d16:1/22:2) levels 8,124 European ancestry individuals NA Affymetrix [15424003] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90199995 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels 8,255 European ancestry individuals NA Affymetrix [15430900] (imputed) 4 Sphingomyelin (d18:1/20:1, d18:2/20:0) measurement http://www.ebi.ac.uk/efo/EFO_0022110 GCST90199996 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl sphingomyelin (d18:1/22:0) levels 8,260 European ancestry individuals NA Affymetrix [15431366] (imputed) 0 behenoyl sphingomyelin (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800376 GCST90199997 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propyl 4-hydroxybenzoate sulfate levels 7,855 European ancestry individuals NA Affymetrix [15416003] (imputed) 0 propyl 4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801005 GCST90199998 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methoxyphenol sulfate levels 7,500 European ancestry individuals NA Affymetrix [15396109] (imputed) 0 4-methoxyphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800080 GCST90199999 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Umbelliferone sulfate levels 5,598 European ancestry individuals NA Affymetrix [15287543] (imputed) 0 umbelliferone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801006 GCST90200000 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels 8,257 European ancestry individuals NA Affymetrix [15431025] (imputed) 6 Sphingomyelin (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0022109 GCST90200001 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-hydroxyindole sulfate levels 8,229 European ancestry individuals NA Affymetrix [15430483] (imputed) 1 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90200002 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol glucuronide levels 7,969 European ancestry individuals NA Affymetrix [15418417] (imputed) 1 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90200003 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) levels 8,257 European ancestry individuals NA Affymetrix [15431122] (imputed) 6 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800409 GCST90200054 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 8,266 European ancestry individuals NA Affymetrix [15430303] (imputed) 3 lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800429 GCST90200055 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/18:0, d19:0/17:0) levels 8,274 European ancestry individuals NA Affymetrix [15431292] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200056 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-gpc (p-16:0/18:1) levels 8,222 European ancestry individuals NA Affymetrix [15428569] (imputed) 4 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800420 GCST90200057 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (p-18:0/20:4) levels 8,254 European ancestry individuals NA Affymetrix [15430980] (imputed) 1 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800415 GCST90200058 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl dihydrosphingomyelin (d18:0/22:0) levels 8,275 European ancestry individuals NA Affymetrix [15430995] (imputed) 4 behenoyl dihydrosphingomyelin (d18:0/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800427 GCST90200059 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (p-16:0/18:2) levels 8,260 European ancestry individuals NA Affymetrix [15431225] (imputed) 1 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800422 GCST90200060 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (p-16:0/18:1) levels 8,264 European ancestry individuals NA Affymetrix [15431701] (imputed) 1 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800419 GCST90200061 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) levels 8,057 European ancestry individuals NA Affymetrix [15422666] (imputed) 2 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800412 GCST90200062 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17367 levels 6,092 European ancestry individuals NA Affymetrix [15321108] (imputed) 1 X-17367 measurement http://www.ebi.ac.uk/efo/EFO_0800779 GCST90200549 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17357 levels 8,041 European ancestry individuals NA Affymetrix [15424327] (imputed) 4 X-17357 measurement http://www.ebi.ac.uk/efo/EFO_0800777 GCST90200550 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18886 levels 8,198 European ancestry individuals NA Affymetrix [15428705] (imputed) 2 X-18886 measurement http://www.ebi.ac.uk/efo/EFO_0800790 GCST90200551 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18887 levels 6,790 European ancestry individuals NA Affymetrix [15368250] (imputed) 0 X-18887 measurement http://www.ebi.ac.uk/efo/EFO_0800791 GCST90200552 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17653 levels 8,025 European ancestry individuals NA Affymetrix [15424164] (imputed) 4 X-17653 measurement http://www.ebi.ac.uk/efo/EFO_0800783 GCST90200553 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17346 levels 6,459 European ancestry individuals NA Affymetrix [15343096] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200554 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17690 levels 7,043 European ancestry individuals NA Affymetrix [15384001] (imputed) 1 X-17690 measurement http://www.ebi.ac.uk/efo/EFO_0800788 GCST90200555 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18345 levels 5,476 European ancestry individuals NA Affymetrix [15278223] (imputed) 0 X-18345 measurement http://www.ebi.ac.uk/efo/EFO_0800789 GCST90200556 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17685 levels 7,327 European ancestry individuals NA Affymetrix [15390006] (imputed) 0 X-17685 measurement http://www.ebi.ac.uk/efo/EFO_0800786 GCST90200557 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18888 levels 6,974 European ancestry individuals NA Affymetrix [15372715] (imputed) 1 X-18888 measurement http://www.ebi.ac.uk/efo/EFO_0800792 GCST90200558 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18901 levels 8,128 European ancestry individuals NA Affymetrix [15427949] (imputed) 0 X-18901 measurement http://www.ebi.ac.uk/efo/EFO_0800794 GCST90200559 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17351 levels 7,281 European ancestry individuals NA Affymetrix [15388868] (imputed) 0 X-17351 measurement http://www.ebi.ac.uk/efo/EFO_0800774 GCST90200560 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18779 levels 8,144 European ancestry individuals NA Affymetrix [15426933] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200561 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21286 levels 8,231 European ancestry individuals NA Affymetrix [15430358] (imputed) 1 X-21286 measurement http://www.ebi.ac.uk/efo/EFO_0800804 GCST90200562 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21355 levels 8,257 European ancestry individuals NA Affymetrix [15430366] (imputed) 0 X-21355 measurement http://www.ebi.ac.uk/efo/EFO_0800810 GCST90200563 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21319 levels 8,109 European ancestry individuals NA Affymetrix [15424361] (imputed) 2 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90200564 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caproate (6:0) levels 7,564 European ancestry individuals NA Affymetrix [15404508] (imputed) 1 caproate 6:0 measurement http://www.ebi.ac.uk/efo/EFO_0021102 GCST90200450 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonadecanoate (19:0) levels 8,231 European ancestry individuals NA Affymetrix [15430042] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90200451 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free asparagine levels 8,245 European ancestry individuals NA Affymetrix [15430003] (imputed) 3 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90200452 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-07765 levels 8,127 European ancestry individuals NA Affymetrix [15427497] (imputed) 1 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90200453 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate levels 8,212 European ancestry individuals NA Affymetrix [15429217] (imputed) 1 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90200455 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11308 levels 8,253 European ancestry individuals NA Affymetrix [15430735] (imputed) 4 X-11308 measurement http://www.ebi.ac.uk/efo/EFO_0800693 GCST90200456 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentadecanoate (15:0) levels 8,273 European ancestry individuals NA Affymetrix [15431327] (imputed) 0 pentadecanoate 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021073 GCST90200457 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11315 levels 8,139 European ancestry individuals NA Affymetrix [15426875] (imputed) 4 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90200458 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margarate (17:0) levels 8,279 European ancestry individuals NA Affymetrix [15431582] (imputed) 0 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90200459 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11372 levels 8,251 European ancestry individuals NA Affymetrix [15431068] (imputed) 3 X-11372 measurement http://www.ebi.ac.uk/efo/EFO_0800694 GCST90200460 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-10458 levels 7,970 European ancestry individuals NA Affymetrix [15418298] (imputed) 1 X-10458 measurement http://www.ebi.ac.uk/efo/EFO_0800692 GCST90200461 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11299 levels 8,203 European ancestry individuals NA Affymetrix [15429423] (imputed) 1 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90200462 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11478 levels 8,242 European ancestry individuals NA Affymetrix [15430075] (imputed) 2 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90200463 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11849 levels 7,679 European ancestry individuals NA Affymetrix [15411690] (imputed) 1 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90200464 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11787 levels 8,247 European ancestry individuals NA Affymetrix [15431000] (imputed) 3 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90200465 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11632 levels 7,784 European ancestry individuals NA Affymetrix [15414129] (imputed) 0 X-11632 measurement http://www.ebi.ac.uk/efo/EFO_0800697 GCST90200466 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11852 levels 7,295 European ancestry individuals NA Affymetrix [15394910] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90200467 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11847 levels 7,193 European ancestry individuals NA Affymetrix [15389923] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90200468 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11483 levels 7,798 European ancestry individuals NA Affymetrix [15415518] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90200469 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11470 levels 8,134 European ancestry individuals NA Affymetrix [15425746] (imputed) 6 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90200470 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11381 levels 8,225 European ancestry individuals NA Affymetrix [15430300] (imputed) 6 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90200471 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11850 levels 7,629 European ancestry individuals NA Affymetrix [15404183] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90200472 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11795 levels 8,238 European ancestry individuals NA Affymetrix [15430933] (imputed) 1 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90200473 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11444 levels 8,206 European ancestry individuals NA Affymetrix [15428503] (imputed) 5 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90200474 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11858 levels 6,008 European ancestry individuals NA Affymetrix [15331917] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90200475 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-14056 levels 8,242 European ancestry individuals NA Affymetrix [15430238] (imputed) 0 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90200526 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13866 levels 8,252 European ancestry individuals NA Affymetrix [15430990] (imputed) 2 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90200527 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17146 levels 7,778 European ancestry individuals NA Affymetrix [15413146] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200528 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16397 levels 8,057 European ancestry individuals NA Affymetrix [15424887] (imputed) 1 X-16397 measurement http://www.ebi.ac.uk/efo/EFO_0800758 GCST90200529 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17335 levels 7,747 European ancestry individuals NA Affymetrix [15411378] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90200530 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16964 levels 8,048 European ancestry individuals NA Affymetrix [15424085] (imputed) 0 X-16964 measurement http://www.ebi.ac.uk/efo/EFO_0020011 GCST90200531 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16935 levels 7,804 European ancestry individuals NA Affymetrix [15413446] (imputed) 5 X-16935 measurement http://www.ebi.ac.uk/efo/EFO_0800763 GCST90200532 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15486 levels 8,236 European ancestry individuals NA Affymetrix [15430469] (imputed) 1 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90200533 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16580 levels 8,254 European ancestry individuals NA Affymetrix [15431135] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90200534 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17325 levels 7,448 European ancestry individuals NA Affymetrix [15398826] (imputed) 1 X-17325 measurement http://www.ebi.ac.uk/efo/EFO_0800771 GCST90200535 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17328 levels 5,856 European ancestry individuals NA Affymetrix [15309442] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200536 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16087 levels 7,071 European ancestry individuals NA Affymetrix [15383204] (imputed) 2 X-16087 measurement http://www.ebi.ac.uk/efo/EFO_0800756 GCST90200537 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17010 levels 7,879 European ancestry individuals NA Affymetrix [15416580] (imputed) 0 X-17010 measurement http://www.ebi.ac.uk/efo/EFO_0800767 GCST90200538 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-14939 levels 8,250 European ancestry individuals NA Affymetrix [15431307] (imputed) 1 X-14939 measurement http://www.ebi.ac.uk/efo/EFO_0800747 GCST90200539 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15461 levels 8,144 European ancestry individuals NA Affymetrix [15427795] (imputed) 0 X-15461 measurement http://www.ebi.ac.uk/efo/EFO_0800749 GCST90200540 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15523 levels 8,071 European ancestry individuals NA Affymetrix [15424746] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200541 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15728 levels 7,874 European ancestry individuals NA Affymetrix [15413966] (imputed) 0 X-15728 measurement http://www.ebi.ac.uk/efo/EFO_0020024 GCST90200542 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15503 levels 8,237 European ancestry individuals NA Affymetrix [15429705] (imputed) 2 X-15503 measurement http://www.ebi.ac.uk/efo/EFO_0800753 GCST90200543 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16124 levels 5,337 European ancestry individuals NA Affymetrix [15272312] (imputed) 0 X-16124 measurement http://www.ebi.ac.uk/efo/EFO_0800757 GCST90200544 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17438 levels 6,913 European ancestry individuals NA Affymetrix [15365729] (imputed) 0 X-17438 measurement http://www.ebi.ac.uk/efo/EFO_0800781 GCST90200545 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17354 levels 5,375 European ancestry individuals NA Affymetrix [15269880] (imputed) 0 X-17354 measurement http://www.ebi.ac.uk/efo/EFO_0800776 GCST90200546 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17654 levels 7,690 European ancestry individuals NA Affymetrix [15408966] (imputed) 5 X-17654 measurement http://www.ebi.ac.uk/efo/EFO_0800784 GCST90200547 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17676 levels 8,118 European ancestry individuals NA Affymetrix [15427039] (imputed) 4 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90200548 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminoheptanoate levels 8,238 European ancestry individuals NA Affymetrix [15431100] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90199952 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxytyramine sulfate levels 5,419 European ancestry individuals NA Affymetrix [15273345] (imputed) 0 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90199953 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21258 levels 8,198 European ancestry individuals NA Affymetrix [15428505] (imputed) 1 X-21258 measurement http://www.ebi.ac.uk/efo/EFO_0800802 GCST90200565 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21364 levels 8,203 European ancestry individuals NA Affymetrix [15429064] (imputed) 1 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90200566 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21353 levels 8,265 European ancestry individuals NA Affymetrix [15431194] (imputed) 1 X-21353 measurement http://www.ebi.ac.uk/efo/EFO_0800809 GCST90200567 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19438 levels 7,259 European ancestry individuals NA Affymetrix [15387392] (imputed) 0 X-19438 measurement http://www.ebi.ac.uk/efo/EFO_0800801 GCST90200568 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18913 levels 8,271 European ancestry individuals NA Affymetrix [15431181] (imputed) 1 X-18913 measurement http://www.ebi.ac.uk/efo/EFO_0800795 GCST90200569 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18921 levels 8,257 European ancestry individuals NA Affymetrix [15430800] (imputed) 3 X-18921 measurement http://www.ebi.ac.uk/efo/EFO_0800796 GCST90200570 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21339 levels 8,203 European ancestry individuals NA Affymetrix [15428402] (imputed) 1 X-21339 measurement http://www.ebi.ac.uk/efo/EFO_0800808 GCST90200571 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19299 levels 6,100 European ancestry individuals NA Affymetrix [15329664] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200572 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18935 levels 4,952 European ancestry individuals NA Affymetrix [15465872] (imputed) 1 X-18935 measurement http://www.ebi.ac.uk/efo/EFO_0800798 GCST90200573 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21310 levels 7,801 European ancestry individuals NA Affymetrix [15413292] (imputed) 0 X-21310 measurement http://www.ebi.ac.uk/efo/EFO_0800805 GCST90200574 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21283 levels 7,055 European ancestry individuals NA Affymetrix [15374688] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200575 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21285 levels 6,180 European ancestry individuals NA Affymetrix [15333546] (imputed) 2 X-21285 measurement http://www.ebi.ac.uk/efo/EFO_0800803 GCST90200576 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21312 levels 4,897 European ancestry individuals NA Affymetrix [15466547] (imputed) 1 X-21312 measurement http://www.ebi.ac.uk/efo/EFO_0800806 GCST90200577 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18922 levels 8,174 European ancestry individuals NA Affymetrix [15428317] (imputed) 4 X-18922 measurement http://www.ebi.ac.uk/efo/EFO_0800797 GCST90200578 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21442 levels 6,827 European ancestry individuals NA Affymetrix [15368219] (imputed) 1 X-21442 measurement http://www.ebi.ac.uk/efo/EFO_0800815 GCST90200579 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21796 levels 8,130 European ancestry individuals NA Affymetrix [15425387] (imputed) 2 X-21796 measurement http://www.ebi.ac.uk/efo/EFO_0800825 GCST90200580 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21441 levels 8,030 European ancestry individuals NA Affymetrix [15424784] (imputed) 7 X-21441 measurement http://www.ebi.ac.uk/efo/EFO_0800814 GCST90200581 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21752 levels 6,526 European ancestry individuals NA Affymetrix [15349894] (imputed) 0 X-21752 measurement http://www.ebi.ac.uk/efo/EFO_0800824 GCST90200582 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21807 levels 5,602 European ancestry individuals NA Affymetrix [15278260] (imputed) 0 X-21807 measurement http://www.ebi.ac.uk/efo/EFO_0800827 GCST90200583 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21736 levels 8,232 European ancestry individuals NA Affymetrix [15430245] (imputed) 1 X-21736 measurement http://www.ebi.ac.uk/efo/EFO_0800821 GCST90200584 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21829 levels 8,217 European ancestry individuals NA Affymetrix [15429228] (imputed) 3 X-21829 measurement http://www.ebi.ac.uk/efo/EFO_0800830 GCST90200585 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21471 levels 7,982 European ancestry individuals NA Affymetrix [15419165] (imputed) 6 X-21471 measurement http://www.ebi.ac.uk/efo/EFO_0800818 GCST90200586 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21733 levels 6,916 European ancestry individuals NA Affymetrix [15375208] (imputed) 0 X-21733 measurement http://www.ebi.ac.uk/efo/EFO_0800820 GCST90200587 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21742 levels 5,918 European ancestry individuals NA Affymetrix [15306712] (imputed) 0 X-21742 measurement http://www.ebi.ac.uk/efo/EFO_0800823 GCST90200588 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21821 levels 7,699 European ancestry individuals NA Affymetrix [15408996] (imputed) 0 X-21821 measurement http://www.ebi.ac.uk/efo/EFO_0800829 GCST90200589 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12731 levels 5,770 European ancestry individuals NA Affymetrix [15306286] (imputed) 0 X-12731 measurement http://www.ebi.ac.uk/efo/EFO_0800725 GCST90200501 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12707 levels 7,461 European ancestry individuals NA Affymetrix [15399335] (imputed) 7 X-12707 measurement http://www.ebi.ac.uk/efo/EFO_0800720 GCST90200502 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12729 levels 7,446 European ancestry individuals NA Affymetrix [15399983] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90200503 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12830 levels 5,725 European ancestry individuals NA Affymetrix [15295616] (imputed) 0 X-12830 measurement http://www.ebi.ac.uk/efo/EFO_0021337 GCST90200504 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12818 levels 6,246 European ancestry individuals NA Affymetrix [15326545] (imputed) 0 X-12818 measurement http://www.ebi.ac.uk/efo/EFO_0800729 GCST90200505 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12812 levels 6,435 European ancestry individuals NA Affymetrix [15342139] (imputed) 0 X-12812 measurement http://www.ebi.ac.uk/efo/EFO_0800728 GCST90200506 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12822 levels 7,957 European ancestry individuals NA Affymetrix [15420736] (imputed) 2 X-12822 measurement http://www.ebi.ac.uk/efo/EFO_0800730 GCST90200507 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12738 levels 5,874 European ancestry individuals NA Affymetrix [15304194] (imputed) 0 X-12738 measurement http://www.ebi.ac.uk/efo/EFO_0800726 GCST90200508 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12544 levels 7,471 European ancestry individuals NA Affymetrix [15399646] (imputed) 1 X-12544 measurement http://www.ebi.ac.uk/efo/EFO_0021315 GCST90200509 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12680 levels 8,255 European ancestry individuals NA Affymetrix [15430396] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90200510 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12906 levels 7,896 European ancestry individuals NA Affymetrix [15416798] (imputed) 0 X-12906 measurement http://www.ebi.ac.uk/efo/EFO_0800733 GCST90200511 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13684 levels 8,112 European ancestry individuals NA Affymetrix [15426792] (imputed) 5 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90200512 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13507 levels 7,936 European ancestry individuals NA Affymetrix [15418372] (imputed) 0 X-13507 measurement http://www.ebi.ac.uk/efo/EFO_0800736 GCST90200513 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12851 levels 7,385 European ancestry individuals NA Affymetrix [15395726] (imputed) 1 X-12851 measurement http://www.ebi.ac.uk/efo/EFO_0021342 GCST90200514 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12849 levels 7,555 European ancestry individuals NA Affymetrix [15404109] (imputed) 0 X-12849 measurement http://www.ebi.ac.uk/efo/EFO_0800732 GCST90200515 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12847 levels 7,790 European ancestry individuals NA Affymetrix [15413150] (imputed) 1 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90200516 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13553 levels 8,118 European ancestry individuals NA Affymetrix [15425695] (imputed) 0 X-13553 measurement http://www.ebi.ac.uk/efo/EFO_0021355 GCST90200517 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12839 levels 4,867 European ancestry individuals NA Affymetrix [15458356] (imputed) 1 X-12839 measurement http://www.ebi.ac.uk/efo/EFO_0800731 GCST90200518 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13729 levels 7,724 European ancestry individuals NA Affymetrix [15410706] (imputed) 1 X-13729 measurement http://www.ebi.ac.uk/efo/EFO_0800742 GCST90200519 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13007 levels 6,270 European ancestry individuals NA Affymetrix [15341748] (imputed) 0 X-13007 measurement http://www.ebi.ac.uk/efo/EFO_0800734 GCST90200520 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13844 levels 7,501 European ancestry individuals NA Affymetrix [15398992] (imputed) 0 X-13844 measurement http://www.ebi.ac.uk/efo/EFO_0800744 GCST90200521 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13728 levels 7,905 European ancestry individuals NA Affymetrix [15420146] (imputed) 0 X-13728 measurement http://www.ebi.ac.uk/efo/EFO_0800741 GCST90200522 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12844 levels 8,231 European ancestry individuals NA Affymetrix [15429689] (imputed) 5 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90200523 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13695 levels 6,486 European ancestry individuals NA Affymetrix [15350858] (imputed) 0 X-13695 measurement http://www.ebi.ac.uk/efo/EFO_0800738 GCST90200524 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13723 levels 5,269 European ancestry individuals NA Affymetrix [15258271] (imputed) 0 X-13723 measurement http://www.ebi.ac.uk/efo/EFO_0800739 GCST90200525 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-gpc (16:0/18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90202770 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels 101 East Asian ancestry individuals NA Affymetrix [4330921] (imputed) 0 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800609 GCST90202771 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetate levels 99 East Asian ancestry individuals NA Affymetrix [4199615] (imputed) 0 4-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800124 GCST90202772 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurodeoxycholate levels 76 East Asian ancestry individuals NA Affymetrix [4228162] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90202773 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleate (18:2n6) levels 103 East Asian ancestry individuals NA Affymetrix [4301369] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90202774 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90202775 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,n6,n6-trimethyllysine levels 103 East Asian ancestry individuals NA Affymetrix [4303061] (imputed) 0 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90202776 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholic acid levels 97 East Asian ancestry individuals NA Affymetrix [4230279] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90202777 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9,10-DiHOME levels 96 East Asian ancestry individuals NA Affymetrix [4254053] (imputed) 0 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90202778 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyhippurate (salicylurate) levels 101 East Asian ancestry individuals NA Affymetrix [4336840] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90202779 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Laurate (12:0) levels 102 East Asian ancestry individuals NA Affymetrix [4314243] (imputed) 0 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90202780 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90202781 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5,6-dihydrothymine levels 103 East Asian ancestry individuals NA Affymetrix [4301844] (imputed) 0 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90202782 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholate levels 103 East Asian ancestry individuals NA Affymetrix [4302736] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90202783 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylputrescine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90202784 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingosine (d18:1/18:0) levels 103 East Asian ancestry individuals NA Affymetrix [4299732] (imputed) 0 N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800613 GCST90202785 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovalerate levels 102 East Asian ancestry individuals NA Affymetrix [4321371] (imputed) 0 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90202786 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylmethionine levels 103 East Asian ancestry individuals NA Affymetrix [4298757] (imputed) 0 N-formylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800128 GCST90202787 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine levels 103 East Asian ancestry individuals NA Affymetrix [4298757] (imputed) 0 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90202788 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosapentaenoate (EPA; 20:5n3) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 eicosapentaenoate (EPA; 20:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800616 GCST90202789 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-adenosylhomocysteine (SAH) levels 78 East Asian ancestry individuals NA Affymetrix [4199014] (imputed) 0 S-adenosylhomocysteine measurement http://www.ebi.ac.uk/efo/EFO_0010531 GCST90202790 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Biliverdin levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90202791 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyphenylacetate levels 92 East Asian ancestry individuals NA Affymetrix [4307060] (imputed) 0 2-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800131 GCST90202792 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90202793 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate levels 103 East Asian ancestry individuals NA Affymetrix [4299170] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90202794 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(4-hydroxyphenyl)lactate levels 103 East Asian ancestry individuals NA Affymetrix [4303357] (imputed) 0 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90202795 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinate levels 96 East Asian ancestry individuals NA Affymetrix [4257829] (imputed) 0 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90202796 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylmalonate levels 103 East Asian ancestry individuals NA Affymetrix [4302736] (imputed) 0 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90202797 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 3',5'-cyclic monophosphate (camp) levels 88 East Asian ancestry individuals NA Affymetrix [4204568] (imputed) 0 cyclic adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010473 GCST90202798 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methylthioadenosine (mta) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90202799 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Adenosine 5'-monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0021574 GCST90202800 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinate levels 98 East Asian ancestry individuals NA Affymetrix [4212608] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90202801 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphocholine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90202802 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90202803 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-Hydroxybutyrate levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90202804 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-alanine levels 100 East Asian ancestry individuals NA Affymetrix [4343943] (imputed) 0 beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0800640 GCST90202805 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylpyruvate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 phenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800132 GCST90202806 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Flavin adenine dinucleotide (FAD) levels 76 East Asian ancestry individuals NA Affymetrix [4241927] (imputed) 0 flavin adenine dinucleotide (FAD) measurement http://www.ebi.ac.uk/efo/EFO_0800177 GCST90202807 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatinine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90202808 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholate levels 103 East Asian ancestry individuals NA Affymetrix [4298892] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90202809 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisone levels 102 East Asian ancestry individuals NA Affymetrix [4313550] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90202810 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholate levels 89 East Asian ancestry individuals NA Affymetrix [4191668] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90202811 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine levels 103 East Asian ancestry individuals NA Affymetrix [4298993] (imputed) 0 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90202812 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystine levels 100 East Asian ancestry individuals NA Affymetrix [4354722] (imputed) 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90202813 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisol levels (plasma) 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90202814 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine levels 101 East Asian ancestry individuals NA Affymetrix [4337850] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90202815 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphinganine levels 93 East Asian ancestry individuals NA Affymetrix [4304237] (imputed) 0 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90202816 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystathionine levels 100 East Asian ancestry individuals NA Affymetrix [4350018] (imputed) 0 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90202817 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gluconate levels 102 East Asian ancestry individuals NA Affymetrix [4317421] (imputed) 0 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90202818 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine levels 100 East Asian ancestry individuals NA Affymetrix [4354952] (imputed) 0 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90202819 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminobutyrate levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90202745 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90202746 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-3-methylglutarate levels 99 East Asian ancestry individuals NA Affymetrix [4192772] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90202747 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homovanillate (hva) levels 82 East Asian ancestry individuals NA Affymetrix [4328807] (imputed) 0 HVA measurement http://www.ebi.ac.uk/efo/EFO_0005131 GCST90202748 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Anthranilate levels 53 East Asian ancestry individuals NA Affymetrix [4284740] (imputed) 0 anthranilate measurement http://www.ebi.ac.uk/efo/EFO_0800123 GCST90202749 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylneuraminate levels 102 East Asian ancestry individuals NA Affymetrix [4317062] (imputed) 0 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90202750 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosaminylasparagine levels 103 East Asian ancestry individuals NA Affymetrix [4300838] (imputed) 0 N-acetylglucosaminylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800151 GCST90202751 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl ethanolamide levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 oleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800604 GCST90202752 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamine levels 103 East Asian ancestry individuals NA Affymetrix [4300329] (imputed) 0 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90202753 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylpyruvate levels 96 East Asian ancestry individuals NA Affymetrix [4240235] (imputed) 0 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90202754 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetoacetate levels 90 East Asian ancestry individuals NA Affymetrix [4350773] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90202755 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90202756 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cys-gly, oxidized levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90202757 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linoleate (20:2n6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90202758 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol levels 103 East Asian ancestry individuals NA Affymetrix [4301369] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90202759 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Choline levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90202760 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxystearate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90202761 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phosphoglycerate levels 103 East Asian ancestry individuals NA Affymetrix [4301256] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90202762 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylleucine levels 98 East Asian ancestry individuals NA Affymetrix [4205716] (imputed) 0 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90202763 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate levels 101 East Asian ancestry individuals NA Affymetrix [4331128] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90202764 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylhistidine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90202765 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N1-methyladenosine levels 103 East Asian ancestry individuals NA Affymetrix [4303044] (imputed) 0 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90202766 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrate/isobutyrate (4:0) levels 101 East Asian ancestry individuals NA Affymetrix [4333562] (imputed) 0 isobutyrate (4:0) measurement http://www.ebi.ac.uk/efo/EFO_0800605 GCST90202767 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinolinate levels 103 East Asian ancestry individuals NA Affymetrix [4300809] (imputed) 0 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90202768 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoyl sphingomyelin (d18:1/18:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 stearoyl sphingomyelin (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800611 GCST90202769 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pristanate levels 75 East Asian ancestry individuals NA Affymetrix [4270137] (imputed) 0 pristanate measurement http://www.ebi.ac.uk/efo/EFO_0800623 GCST90202845 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phytanate levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 phytanate measurement http://www.ebi.ac.uk/efo/EFO_0801065 GCST90202846 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-deoxyuridine levels 100 East Asian ancestry individuals NA Affymetrix [4349641] (imputed) 0 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90202847 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonine levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90202848 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Valine levels 102 East Asian ancestry individuals NA Affymetrix [4316963] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90202849 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Blood sugar levels 103 East Asian ancestry individuals NA Affymetrix [4298892] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90202850 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Retinol (Vitamin A) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90202851 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 12,13-DiHOME levels 103 East Asian ancestry individuals NA Affymetrix [4298757] (imputed) 0 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90202852 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate levels 102 East Asian ancestry individuals NA Affymetrix [4321724] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90202853 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urea levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90202854 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serotonin levels 92 East Asian ancestry individuals NA Affymetrix [4308028] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90202855 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Uridine levels 103 East Asian ancestry individuals NA Affymetrix [4301329] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90202856 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90202857 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine levels 97 East Asian ancestry individuals NA Affymetrix [4225117] (imputed) 0 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90202858 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylnicotinamide levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90202859 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristate (14:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90202860 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90202861 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90202862 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan levels 103 East Asian ancestry individuals NA Affymetrix [4301160] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90202863 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-urocanate levels 103 East Asian ancestry individuals NA Affymetrix [4301972] (imputed) 0 trans-urocanate measurement http://www.ebi.ac.uk/efo/EFO_0800138 GCST90202864 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyruvate levels 103 East Asian ancestry individuals NA Affymetrix [4300066] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90202865 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margarate (17:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90202866 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Betaine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90202867 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caprate (10:0) levels 103 East Asian ancestry individuals NA Affymetrix [4299351] (imputed) 0 caprate 10:0 measurement http://www.ebi.ac.uk/efo/EFO_0021101 GCST90202868 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonadecanoate (19:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90202869 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeine levels 99 East Asian ancestry individuals NA Affymetrix [4195901] (imputed) 0 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90202870 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xylose levels 86 East Asian ancestry individuals NA Affymetrix [4250957] (imputed) 0 xylose measurement http://www.ebi.ac.uk/efo/EFO_0800153 GCST90202871 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytidine levels 80 East Asian ancestry individuals NA Affymetrix [4382929] (imputed) 0 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90202872 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pseudouridine levels 102 East Asian ancestry individuals NA Affymetrix [4317062] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90202873 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyrosine levels 102 East Asian ancestry individuals NA Affymetrix [4318415] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90202874 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate levels 98 East Asian ancestry individuals NA Affymetrix [4204495] (imputed) 0 alpha-ketobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800140 GCST90202875 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructose levels 102 East Asian ancestry individuals NA Affymetrix [4320222] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90202876 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine levels 102 East Asian ancestry individuals NA Affymetrix [4316091] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90202877 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alanine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90202878 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethylglycine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90202879 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose levels 102 East Asian ancestry individuals NA Affymetrix [4316123] (imputed) 0 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90202880 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maltose levels in coronary artery disease 79 East Asian ancestry individuals NA Affymetrix [4159158] (imputed) 0 Maltose measurement http://www.ebi.ac.uk/efo/EFO_0021649 GCST90202881 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free asparagine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90202882 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidate (20:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 arachidate (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800625 GCST90202883 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytosine levels 88 East Asian ancestry individuals NA Affymetrix [4197784] (imputed) 0 blood cytosine measurement http://www.ebi.ac.uk/efo/EFO_0022213 GCST90202884 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentadecanoate (15:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 pentadecanoate 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021073 GCST90202885 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caproate (6:0) levels 100 East Asian ancestry individuals NA Affymetrix [4345893] (imputed) 0 caproate 6:0 measurement http://www.ebi.ac.uk/efo/EFO_0021102 GCST90202886 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate levels 103 East Asian ancestry individuals NA Affymetrix [4298954] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90202887 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sucrose levels 97 East Asian ancestry individuals NA Affymetrix [4238542] (imputed) 0 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90202888 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenate levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90202889 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphinganine (d18:0/18:0) levels 84 East Asian ancestry individuals NA Affymetrix [4290009] (imputed) 0 N-stearoyl-sphinganine (d18:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800626 GCST90202890 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-07765 levels 101 East Asian ancestry individuals NA Affymetrix [4336250] (imputed) 0 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90202891 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caprylate (8:0) levels 102 East Asian ancestry individuals NA Affymetrix [4313947] (imputed) 0 caprylate 8:0 measurement http://www.ebi.ac.uk/efo/EFO_0021103 GCST90202892 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-10458 levels 103 East Asian ancestry individuals NA Affymetrix [4301844] (imputed) 0 X-10458 measurement http://www.ebi.ac.uk/efo/EFO_0800692 GCST90202893 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11444 levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90202894 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hypotaurine levels 103 East Asian ancestry individuals NA Affymetrix [4299641] (imputed) 0 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90202820 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarate (C5-DC) levels 101 East Asian ancestry individuals NA Affymetrix [4332337] (imputed) 0 glutarate (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800620 GCST90202821 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90202822 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guanidinoacetate levels 103 East Asian ancestry individuals NA Affymetrix [4298757] (imputed) 0 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90202823 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamate levels 103 East Asian ancestry individuals NA Affymetrix [4298015] (imputed) 0 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90202824 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine levels 58 East Asian ancestry individuals NA Affymetrix [4138346] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90202825 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-1-pyrroline-5-carboxylate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90202826 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoleucine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90202827 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nicotinamide levels 101 East Asian ancestry individuals NA Affymetrix [4337680] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90202828 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylalanine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90202829 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrulline levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90202830 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Leucine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90202831 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lysine levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90202832 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Malate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90202833 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitate (16:0) levels 103 East Asian ancestry individuals NA Affymetrix [4301369] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90202834 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine levels 102 East Asian ancestry individuals NA Affymetrix [4317756] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90202835 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma lactate levels 102 East Asian ancestry individuals NA Affymetrix [4318130] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90202836 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myo-inositol levels 102 East Asian ancestry individuals NA Affymetrix [4320050] (imputed) 0 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90202837 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free proline levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90202838 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearate (18:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90202839 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ornithine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90202840 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotate levels 102 East Asian ancestry individuals NA Affymetrix [4317332] (imputed) 0 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90202841 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyridoxal levels 103 East Asian ancestry individuals NA Affymetrix [4300441] (imputed) 0 blood pyridoxal measurement http://www.ebi.ac.uk/efo/EFO_0022222 GCST90202842 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoleate (16:1n7) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90202843 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate levels (UKB data field 30810) 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90202844 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12844 levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90202945 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12822 levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 X-12822 measurement http://www.ebi.ac.uk/efo/EFO_0800730 GCST90202946 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12847 levels 92 East Asian ancestry individuals NA Affymetrix [4317122] (imputed) 0 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90202947 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12851 levels 80 East Asian ancestry individuals NA Affymetrix [4371063] (imputed) 0 X-12851 measurement http://www.ebi.ac.uk/efo/EFO_0021342 GCST90202948 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13007 levels 92 East Asian ancestry individuals NA Affymetrix [4314487] (imputed) 0 X-13007 measurement http://www.ebi.ac.uk/efo/EFO_0800734 GCST90202949 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15461 levels 102 East Asian ancestry individuals NA Affymetrix [4313107] (imputed) 0 X-15461 measurement http://www.ebi.ac.uk/efo/EFO_0800749 GCST90202950 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-14056 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90202951 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-14939 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-14939 measurement http://www.ebi.ac.uk/efo/EFO_0800747 GCST90202952 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12906 levels 97 East Asian ancestry individuals NA Affymetrix [4223472] (imputed) 0 X-12906 measurement http://www.ebi.ac.uk/efo/EFO_0800733 GCST90202953 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13866 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90202954 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13844 levels 82 East Asian ancestry individuals NA Affymetrix [4352913] (imputed) 0 X-13844 measurement http://www.ebi.ac.uk/efo/EFO_0800744 GCST90202955 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13553 levels 103 East Asian ancestry individuals NA Affymetrix [4301844] (imputed) 0 X-13553 measurement http://www.ebi.ac.uk/efo/EFO_0021355 GCST90202956 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13728 levels 98 East Asian ancestry individuals NA Affymetrix [4219891] (imputed) 0 X-13728 measurement http://www.ebi.ac.uk/efo/EFO_0800741 GCST90202957 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13695 levels 81 East Asian ancestry individuals NA Affymetrix [4358866] (imputed) 0 X-13695 measurement http://www.ebi.ac.uk/efo/EFO_0800738 GCST90202958 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13507 levels 98 East Asian ancestry individuals NA Affymetrix [4210672] (imputed) 0 X-13507 measurement http://www.ebi.ac.uk/efo/EFO_0800736 GCST90202959 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13684 levels 100 East Asian ancestry individuals NA Affymetrix [4351327] (imputed) 0 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90202960 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13431 levels 98 East Asian ancestry individuals NA Affymetrix [4210182] (imputed) 0 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90202961 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17328 levels 64 East Asian ancestry individuals NA Affymetrix [4271067] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202962 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17438 levels 79 East Asian ancestry individuals NA Affymetrix [4171367] (imputed) 0 X-17438 measurement http://www.ebi.ac.uk/efo/EFO_0800781 GCST90202963 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16124 levels 60 East Asian ancestry individuals NA Affymetrix [4378778] (imputed) 0 X-16124 measurement http://www.ebi.ac.uk/efo/EFO_0800757 GCST90202964 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17346 levels 73 East Asian ancestry individuals NA Affymetrix [4315989] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202965 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16087 levels 86 East Asian ancestry individuals NA Affymetrix [4238538] (imputed) 0 X-16087 measurement http://www.ebi.ac.uk/efo/EFO_0800756 GCST90202966 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17146 levels 95 East Asian ancestry individuals NA Affymetrix [4262801] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202967 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17367 levels 63 East Asian ancestry individuals NA Affymetrix [4315243] (imputed) 0 X-17367 measurement http://www.ebi.ac.uk/efo/EFO_0800779 GCST90202968 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16397 levels 99 East Asian ancestry individuals NA Affymetrix [4196160] (imputed) 0 X-16397 measurement http://www.ebi.ac.uk/efo/EFO_0800758 GCST90202969 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12193 levels 100 East Asian ancestry individuals NA Affymetrix [4353417] (imputed) 0 X-12193 measurement http://www.ebi.ac.uk/efo/EFO_0800710 GCST90202920 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12101 levels 102 East Asian ancestry individuals NA Affymetrix [4315309] (imputed) 0 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90202921 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12112 levels 102 East Asian ancestry individuals NA Affymetrix [4318666] (imputed) 0 X-12112 measurement http://www.ebi.ac.uk/efo/EFO_0800705 GCST90202922 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12100 levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 X-12100 measurement http://www.ebi.ac.uk/efo/EFO_0800701 GCST90202923 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12117 levels 70 East Asian ancestry individuals NA Affymetrix [4367733] (imputed) 0 X-12117 measurement http://www.ebi.ac.uk/efo/EFO_0800706 GCST90202924 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12104 levels 88 East Asian ancestry individuals NA Affymetrix [4198298] (imputed) 0 X-12104 measurement http://www.ebi.ac.uk/efo/EFO_0800703 GCST90202925 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12127 levels 79 East Asian ancestry individuals NA Affymetrix [4150092] (imputed) 0 X-12127 measurement http://www.ebi.ac.uk/efo/EFO_0800709 GCST90202926 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12407 levels 86 East Asian ancestry individuals NA Affymetrix [4255535] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90202927 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12411 levels 103 East Asian ancestry individuals NA Affymetrix [4300441] (imputed) 0 X-12411 measurement http://www.ebi.ac.uk/efo/EFO_0800716 GCST90202928 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12714 levels 78 East Asian ancestry individuals NA Affymetrix [4199027] (imputed) 0 X-12714 measurement http://www.ebi.ac.uk/efo/EFO_0800722 GCST90202929 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12731 levels 69 East Asian ancestry individuals NA Affymetrix [4154978] (imputed) 0 X-12731 measurement http://www.ebi.ac.uk/efo/EFO_0800725 GCST90202930 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12544 levels 84 East Asian ancestry individuals NA Affymetrix [4277409] (imputed) 0 X-12544 measurement http://www.ebi.ac.uk/efo/EFO_0021315 GCST90202931 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12462 levels 103 East Asian ancestry individuals NA Affymetrix [4301041] (imputed) 0 X-12462 measurement http://www.ebi.ac.uk/efo/EFO_0800717 GCST90202932 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12410 levels 93 East Asian ancestry individuals NA Affymetrix [4307317] (imputed) 0 X-12410 measurement http://www.ebi.ac.uk/efo/EFO_0800715 GCST90202933 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12707 levels 97 East Asian ancestry individuals NA Affymetrix [4233142] (imputed) 0 X-12707 measurement http://www.ebi.ac.uk/efo/EFO_0800720 GCST90202934 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12701 levels 81 East Asian ancestry individuals NA Affymetrix [4349605] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202935 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12680 levels 102 East Asian ancestry individuals NA Affymetrix [4318257] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90202936 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12798 levels 103 East Asian ancestry individuals NA Affymetrix [4300838] (imputed) 0 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90202937 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12740 levels 85 East Asian ancestry individuals NA Affymetrix [4260087] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90202938 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12730 levels 87 East Asian ancestry individuals NA Affymetrix [4236578] (imputed) 0 X-12730 measurement http://www.ebi.ac.uk/efo/EFO_0800724 GCST90202939 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12738 levels 53 East Asian ancestry individuals NA Affymetrix [4337275] (imputed) 0 X-12738 measurement http://www.ebi.ac.uk/efo/EFO_0800726 GCST90202940 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12729 levels 100 East Asian ancestry individuals NA Affymetrix [4350905] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90202941 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12818 levels 78 East Asian ancestry individuals NA Affymetrix [4199668] (imputed) 0 X-12818 measurement http://www.ebi.ac.uk/efo/EFO_0800729 GCST90202942 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12812 levels 81 East Asian ancestry individuals NA Affymetrix [4354184] (imputed) 0 X-12812 measurement http://www.ebi.ac.uk/efo/EFO_0800728 GCST90202943 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12839 levels 56 East Asian ancestry individuals NA Affymetrix [4219100] (imputed) 0 X-12839 measurement http://www.ebi.ac.uk/efo/EFO_0800731 GCST90202944 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11372 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-11372 measurement http://www.ebi.ac.uk/efo/EFO_0800694 GCST90202895 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11308 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-11308 measurement http://www.ebi.ac.uk/efo/EFO_0800693 GCST90202896 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11299 levels 101 East Asian ancestry individuals NA Affymetrix [4335259] (imputed) 0 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90202897 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11632 levels 99 East Asian ancestry individuals NA Affymetrix [4194944] (imputed) 0 X-11632 measurement http://www.ebi.ac.uk/efo/EFO_0800697 GCST90202898 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11843 levels 87 East Asian ancestry individuals NA Affymetrix [4223881] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90202899 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11381 levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90202900 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11478 levels 103 East Asian ancestry individuals NA Affymetrix [4301860] (imputed) 0 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90202901 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11315 levels 103 East Asian ancestry individuals NA Affymetrix [4298892] (imputed) 0 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90202902 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11787 levels 102 East Asian ancestry individuals NA Affymetrix [4319278] (imputed) 0 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90202903 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11483 levels 88 East Asian ancestry individuals NA Affymetrix [4206058] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90202904 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11795 levels 103 East Asian ancestry individuals NA Affymetrix [4300329] (imputed) 0 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90202905 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11470 levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90202906 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11849 levels 103 East Asian ancestry individuals NA Affymetrix [4302909] (imputed) 0 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90202907 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12013 levels 65 East Asian ancestry individuals NA Affymetrix [4267629] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90202908 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12306 levels 68 East Asian ancestry individuals NA Affymetrix [4179575] (imputed) 0 X-12306 measurement http://www.ebi.ac.uk/efo/EFO_0800714 GCST90202909 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12026 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-12026 measurement http://www.ebi.ac.uk/efo/EFO_0800700 GCST90202910 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12283 levels 91 East Asian ancestry individuals NA Affymetrix [4335536] (imputed) 0 X-12283 measurement http://www.ebi.ac.uk/efo/EFO_0800713 GCST90202911 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11850 levels 88 East Asian ancestry individuals NA Affymetrix [4209705] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90202912 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11880 levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 X-11880 measurement http://www.ebi.ac.uk/efo/EFO_0800698 GCST90202913 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12216 levels 94 East Asian ancestry individuals NA Affymetrix [4297047] (imputed) 0 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90202914 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11858 levels 98 East Asian ancestry individuals NA Affymetrix [4207956] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90202915 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11847 levels 101 East Asian ancestry individuals NA Affymetrix [4332428] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90202916 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12007 levels 101 East Asian ancestry individuals NA Affymetrix [4335294] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90202917 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11852 levels 92 East Asian ancestry individuals NA Affymetrix [4328067] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90202918 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12221 levels 78 East Asian ancestry individuals NA Affymetrix [4200892] (imputed) 0 X-12221 measurement http://www.ebi.ac.uk/efo/EFO_0800711 GCST90202919 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4250) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280191 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4255) (Mytilin B) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 mytilin B measurement http://www.ebi.ac.uk/efo/EFO_0803435 GCST90280192 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4257) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280193 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_426) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280194 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4265) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280195 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4267) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280196 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_428) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280197 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4287) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280198 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4289) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280199 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4300) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280200 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4302) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280201 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4314) (Indole-3-acetic-acid-O-glucuronide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 indole-3-acetic-acid-O-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0803424 GCST90280202 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4317) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280203 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4320) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280204 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4323) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280205 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4327) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280206 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4333) (Mercaptoacetyl-Phe-Leu) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 45 mercaptoacetyl-phe-leu measurement http://www.ebi.ac.uk/efo/EFO_0803503 GCST90280207 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4334) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280208 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4337) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280209 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4341) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280210 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4353) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280211 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4356) (N-(11Z-eicosaenoyl)-ethanolamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 level of N-gondoylethanolamine in blood serum http://purl.obolibrary.org/obo/OBA_2045058 GCST90280212 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4358) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280213 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4362) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280214 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4366) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280215 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4957) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280327 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4958) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280328 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4961) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280329 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4962) (N-(9Z12Z15Z-octadecatrienoyl)-glutamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 level of N-linolenoyl glutamine in blood serum http://purl.obolibrary.org/obo/OBA_2045050 GCST90280330 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4963) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280331 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4964) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280332 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4967) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280333 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4971) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280334 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4973) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280335 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4975) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280336 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4980) (6-Hydroxy-5-(4-sulfophenyl)azo-2-naphthalenesulfonic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 6-hydroxy-5-(4-sulfophenyl)azo-2-naphthalenesulfonic acid measurement http://www.ebi.ac.uk/efo/EFO_0803398 GCST90280337 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4981) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280338 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_499) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280339 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4996) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280340 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5014) (Fluocinolone) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 fluocinolone measurement http://www.ebi.ac.uk/efo/EFO_0803498 GCST90280341 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5016) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280342 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5019) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280343 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_502) (Creatinine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90280344 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5025) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280345 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5027) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280346 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5041) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280347 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5045) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280348 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5053) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280349 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5064) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280350 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5277) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279483 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5202) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279468 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5205) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279469 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5217) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279470 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5218) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279471 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_522) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279472 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5228) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279473 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5230) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279474 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5231) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279475 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5239) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279476 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_524) (Oxoglutaric acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279477 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5251) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279478 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5254) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279479 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5255) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279480 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5259) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279481 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_526) (Glutamate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90279482 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4773) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280292 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4774) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280293 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4775) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280294 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_478) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280295 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4784) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280296 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4799) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280297 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4805) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280298 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4812) (N-desmethyltoremifene) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 N-desmethyltoremifene measurement http://www.ebi.ac.uk/efo/EFO_0803437 GCST90280299 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4823) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 78 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280300 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4826) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280301 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5279) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279484 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_528) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279485 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5282) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279486 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5312) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279487 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5315) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279488 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5318) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279489 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5325) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279490 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5327) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279491 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5334) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279492 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5347) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279493 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5349) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279494 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5356) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279495 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5363) (1-eicosyl-2-(4Z7Z10Z13Z16Z19Z-docosahexaenoyl)-glycero-3-phosphoserine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of PS(O-20:0/22:6(4Z,7Z,10Z,13Z,16Z,19Z)) in blood serum http://purl.obolibrary.org/obo/OBA_2045047 GCST90279496 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5367) (1-eicosyl-2-(7Z10Z13Z16Z-docosatetraenoyl)-glycero-3-phosphoserine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 level of PS(O-20:0/22:4(7Z,10Z,13Z,16Z)) in blood serum http://purl.obolibrary.org/obo/OBA_2045045 GCST90279497 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_538) (L-2-Hydroxyglutaric acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 2-hydroxyglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0010446 GCST90279498 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5381) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279499 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_539) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279500 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5393) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279501 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5396) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279502 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5398) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279503 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_54) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279504 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5402) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279505 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5404) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279506 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5409) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279507 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5431) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279508 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_603) ((R)-23-Dihydroxypropane-1-sulfonate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 (R)-23-dihydroxypropane-1-sulfonate measurement http://www.ebi.ac.uk/efo/EFO_0803470 GCST90279575 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_614) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279576 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_619) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279577 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_622) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279578 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_626) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279579 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_630) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279580 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_645) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279581 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_648) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279582 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_65) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279583 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_653) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279584 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_657) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279585 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_658) (Methylarsonic acid monosodium salt) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 methylarsonic acid monosodium salt measurement http://www.ebi.ac.uk/efo/EFO_0803527 GCST90279586 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_663) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279587 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_669) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279588 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_672) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279589 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_673) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279590 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_675) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279591 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_685) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279592 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_686) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279593 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_691) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279594 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_693) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279595 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_699) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279596 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_702) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279597 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_713) (Quinolinic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 quinolinic acid measurement http://www.ebi.ac.uk/efo/EFO_0010528 GCST90279598 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_714) (Demethylphosphinothricin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279599 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4827) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280302 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4829) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280303 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4831) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280304 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4834) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280305 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_484) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280306 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4853) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280307 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4861) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280308 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4874) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280309 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4879) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280310 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4882) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280311 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4883) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280312 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4884) (Mitragynine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280313 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4886) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280314 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4888) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280315 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4896) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280316 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4898) (Mitragynine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280317 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4906) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280318 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4908) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280319 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4922) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280320 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4923) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280321 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4942) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280322 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4945) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280323 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4946) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280324 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4947) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280325 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4952) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280326 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4376) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280216 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4377) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280217 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4378) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280218 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4394) (MG(18:00:00:0)) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280219 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4395) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280220 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4401) (Deacetylcolchicine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280221 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4402) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280222 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4405) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280223 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_441) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280224 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4421) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280225 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4422) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280226 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_444) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280227 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4442) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280228 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4446) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280229 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4447) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280230 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_445) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280231 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4450) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280232 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4451) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280233 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5539) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279543 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5541) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279544 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5543) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279545 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5545) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279546 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5549) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279547 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5556) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279548 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5561) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279549 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5513) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279534 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5515) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279535 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5517) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279536 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5518) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279537 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5522) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279538 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5526) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279539 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5528) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279540 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5533) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279541 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5534) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279542 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4173) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280175 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4175) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280176 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4177) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280177 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4179) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280178 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_418) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280179 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4180) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280180 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4199) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280181 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_42) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280182 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4205) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280183 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4208) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280184 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4209) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280185 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4215) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280186 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4221) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280187 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4238) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280188 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4241) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280189 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4247) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280190 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5434) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279509 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5435) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279510 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5438) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279511 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5446) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279512 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5447) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279513 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_545) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279514 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5453) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279515 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5457) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279516 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5458) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279517 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5466) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279518 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5474) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279519 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5475) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279520 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5476) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279521 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_548) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279522 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5480) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279523 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5483) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279524 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5484) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279525 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5487) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279526 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5490) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279527 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5493) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279528 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5499) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279529 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5501) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279530 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5502) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279531 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5509) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279532 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5510) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279533 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8691) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280987 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8706) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280988 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8709) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280989 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8716) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280990 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8717) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280991 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8720) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280992 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8723) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280993 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8736) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280994 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8737) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280995 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8738) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280996 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8739) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280997 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_874) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280998 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_886) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280999 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_892) (Hypoxanthine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 Hypoxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021604 GCST90281000 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_895) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281001 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_901) (Dimethylphenylenediamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 dimethylphenylenediamine measurement http://www.ebi.ac.uk/efo/EFO_0803496 GCST90281002 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_902) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281003 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_915) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281004 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_917) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281005 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_918) (246-Triaminotoluene) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 246-triaminotoluene measurement http://www.ebi.ac.uk/efo/EFO_0803474 GCST90281006 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_920) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281007 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_943) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281008 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_95) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281009 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_951) (24-Dimethyl-5-vinylthiazole) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 24-dimethyl-5-vinylthiazole measurement http://www.ebi.ac.uk/efo/EFO_0803388 GCST90281010 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_956) (NaNa-Dimethylhistamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 NaNa-dimethylhistamine measurement http://www.ebi.ac.uk/efo/EFO_0803439 GCST90281011 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8409) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280937 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8420) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280938 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8428) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280939 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8434) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280940 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8445) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280941 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8453) (3-phosphoadenosine 5-3-(3R)-3-hydroxy-22-dimethyl-4-(3-(2-(2E)-15-methylhexadec-2-enoylsulfanylethyl)amino-3-oxopropylamino)-4-oxobutyl dihydrogen diphosphate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of (E)-isoheptadec-2-enoyl-CoA in blood serum http://purl.obolibrary.org/obo/OBA_2045056 GCST90280942 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8454) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280943 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8455) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280944 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_847) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280945 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8470) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280946 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8473) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280947 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8477) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280948 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8479) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280949 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8484) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280950 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8486) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280951 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8487) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280952 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8491) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280953 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8496) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280954 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8497) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280955 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8502) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280956 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8505) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280957 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8517) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280958 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8523) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280959 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8544) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280960 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8548) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280961 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8236) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280912 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8246) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280913 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8247) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280914 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8258) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280915 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8262) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280916 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_827) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280917 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8274) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280918 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8282) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280919 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8307) (Sorbitan tristearate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 sorbitan tristearate measurement http://www.ebi.ac.uk/efo/EFO_0803456 GCST90280920 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_831) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280921 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8315) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280922 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8316) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280923 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8337) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280924 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8343) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280925 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8344) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280926 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8346) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280927 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8351) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280928 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8354) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280929 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8356) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280930 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8386) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280931 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8388) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280932 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8393) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280933 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8395) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280934 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_840) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280935 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8406) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280936 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8553) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280962 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_857) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280963 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8575) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280964 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8578) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280965 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8579) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280966 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8589) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280967 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8590) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280968 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8600) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280969 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8608) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280970 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8610) (Arg-vasopressin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280971 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8612) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280972 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8614) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280973 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8616) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280974 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8619) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280975 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8620) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280976 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8621) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280977 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8622) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280978 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8657) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280979 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8658) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280980 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8662) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280981 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8664) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280982 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8667) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280983 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8675) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280984 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8678) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 20 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280985 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_869) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280986 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_96) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281012 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_960) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281013 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_964) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281014 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_97) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281015 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_975) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281016 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_977) (Metenamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 metenamine measurement http://www.ebi.ac.uk/efo/EFO_0803430 GCST90281017 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_992) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281018 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_993) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281019 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_997) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90281020 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenoylcarnitine (C18:3) levels 8,195 European ancestry individuals NA Affymetrix [15427686] (imputed) 2 linolenoylcarnitine (C18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800538 GCST90200132 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Heneicosapentaenoate (21:5n3) levels 4,827 European ancestry individuals NA Affymetrix [15452313] (imputed) 0 heneicosapentaenoate (21:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800537 GCST90200133 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0) levels 8,126 European ancestry individuals NA Affymetrix [15424672] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200134 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidoylcarnitine (C20) levels 7,682 European ancestry individuals NA Affymetrix [15405219] (imputed) 3 arachidoylcarnitine (C20) measurement http://www.ebi.ac.uk/efo/EFO_0800540 GCST90200135 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cerotoylcarnitine (C26) levels 8,266 European ancestry individuals NA Affymetrix [15430482] (imputed) 6 cerotoylcarnitine (C26) measurement http://www.ebi.ac.uk/efo/EFO_0800542 GCST90200136 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroylcarnitine (C24) levels 8,238 European ancestry individuals NA Affymetrix [15430566] (imputed) 5 lignoceroylcarnitine (C24) measurement http://www.ebi.ac.uk/efo/EFO_0800541 GCST90200137 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosatrienoate (22:3n6) levels 5,398 European ancestry individuals NA Affymetrix [15275072] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200138 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenoylcarnitine (C20:3n3 or 6) levels 8,092 European ancestry individuals NA Affymetrix [15423971] (imputed) 8 dihomo-linolenoylcarnitine (C20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800547 GCST90200139 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (2) levels 8,196 European ancestry individuals NA Affymetrix [15429122] (imputed) 2 carotene diol (2) measurement http://www.ebi.ac.uk/efo/EFO_0800171 GCST90200140 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethyl alpha-glucopyranoside levels 6,620 European ancestry individuals NA Affymetrix [15351808] (imputed) 0 ethyl alpha-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801019 GCST90200141 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (1) levels 8,256 European ancestry individuals NA Affymetrix [15430820] (imputed) 2 carotene diol (1) measurement http://www.ebi.ac.uk/efo/EFO_0800170 GCST90200142 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nervonoylcarnitine (C24:1) levels 7,880 European ancestry individuals NA Affymetrix [15414905] (imputed) 5 nervonoylcarnitine (C24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800549 GCST90200143 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linoleoylcarnitine (C20:2) levels 7,887 European ancestry individuals NA Affymetrix [15416363] (imputed) 3 dihomo-linoleoylcarnitine (C20:2) measurement http://www.ebi.ac.uk/efo/EFO_0800546 GCST90200144 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:1/20:0, d16:1/22:0) levels 8,259 European ancestry individuals NA Affymetrix [15431552] (imputed) 6 glycosyl ceramide (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800551 GCST90200145 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoylcarnitine (C22:6) levels 6,287 European ancestry individuals NA Affymetrix [15330077] (imputed) 0 docosahexaenoylcarnitine (C22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800548 GCST90200146 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N,N-trimethyl-5-aminovalerate levels 8,214 European ancestry individuals NA Affymetrix [15429917] (imputed) 6 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90200147 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoylcarnitine (C20:1) levels 8,145 European ancestry individuals NA Affymetrix [15425762] (imputed) 2 eicosenoylcarnitine (C20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800545 GCST90200148 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ximenoylcarnitine (C26:1) levels 8,260 European ancestry individuals NA Affymetrix [15429967] (imputed) 6 ximenoylcarnitine (C26:1) measurement http://www.ebi.ac.uk/efo/EFO_0800543 GCST90200149 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonoylcarnitine (C20:4) levels 8,202 European ancestry individuals NA Affymetrix [15429683] (imputed) 7 arachidonoylcarnitine (C20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800544 GCST90200150 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-dodecenoylcarnitine (C12:1) levels 7,899 European ancestry individuals NA Affymetrix [15419180] (imputed) 1 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90200151 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-butenoylglycine levels 6,253 European ancestry individuals NA Affymetrix [15330859] (imputed) 3 2-butenoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800556 GCST90200152 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (N(1) + N(8))-acetylspermidine levels 8,219 European ancestry individuals NA Affymetrix [15430447] (imputed) 4 blood N(1)-acetylspermidine measurement, blood N(8)-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0022204, http://www.ebi.ac.uk/efo/EFO_0022205 GCST90200153 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxy-cmpf levels 8,254 European ancestry individuals NA Affymetrix [15430070] (imputed) 1 hydroxy-CMPF measurement http://www.ebi.ac.uk/efo/EFO_0800557 GCST90200154 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-furoylcarnitine levels 6,448 European ancestry individuals NA Affymetrix [15344960] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200155 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortolone glucuronide (1) levels 8,152 European ancestry individuals NA Affymetrix [15428140] (imputed) 4 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90200156 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H12O2 levels 6,177 European ancestry individuals NA Affymetrix [15330729] (imputed) 2 glycine conjugate of C10H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800654 GCST90200182 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminooctanoate levels 8,253 European ancestry individuals NA Affymetrix [15430099] (imputed) 2 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90200183 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-formylindole levels 8,256 European ancestry individuals NA Affymetrix [15430066] (imputed) 6 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90200184 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylcitrulline levels 8,163 European ancestry individuals NA Affymetrix [15429219] (imputed) 2 gamma-glutamylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800690 GCST90200185 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 8-methoxykynurenate levels 6,938 European ancestry individuals NA Affymetrix [15372256] (imputed) 0 8-methoxykynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800096 GCST90200186 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienoate (14:2) levels 8,255 European ancestry individuals NA Affymetrix [15430740] (imputed) 1 tetradecadienoate (14:2) measurement http://www.ebi.ac.uk/efo/EFO_0800570 GCST90200187 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-amino-2-piperidone levels 8,237 European ancestry individuals NA Affymetrix [15430421] (imputed) 2 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90200188 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (3) levels 6,512 European ancestry individuals NA Affymetrix [15350454] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801031 GCST90200189 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecadienoate (12:2) levels 8,244 European ancestry individuals NA Affymetrix [15430080] (imputed) 4 dodecadienoate (12:2) measurement http://www.ebi.ac.uk/efo/EFO_0800572 GCST90200190 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl tyrosine levels 6,389 European ancestry individuals NA Affymetrix [15345899] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200191 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N-dimethylalanine levels 8,219 European ancestry individuals NA Affymetrix [15428993] (imputed) 3 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90200192 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethyl beta-glucopyranoside levels 8,152 European ancestry individuals NA Affymetrix [15426555] (imputed) 1 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90200193 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl phenylalanine levels 8,223 European ancestry individuals NA Affymetrix [15430024] (imputed) 0 1-carboxyethylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800101 GCST90200194 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-isoputreanine levels 8,236 European ancestry individuals NA Affymetrix [15430688] (imputed) 7 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90200195 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,2'-Methylenebis(6-tert-butyl-p-cresol) levels 7,397 European ancestry individuals NA Affymetrix [15398141] (imputed) 0 blood 2,2'-Methylenebis(6-tert-butyl-p-cresol) measurement http://www.ebi.ac.uk/efo/EFO_0022208 GCST90200196 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl isoleucine levels 7,526 European ancestry individuals NA Affymetrix [15398773] (imputed) 0 1-carboxyethylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800105 GCST90200197 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxysebacate levels 7,865 European ancestry individuals NA Affymetrix [15414601] (imputed) 2 2-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800571 GCST90200198 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 3-sulfate levels 8,186 European ancestry individuals NA Affymetrix [15427701] (imputed) 0 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90200199 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl valine levels 8,133 European ancestry individuals NA Affymetrix [15425982] (imputed) 1 1-carboxyethylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800103 GCST90200200 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-bromotryptophan levels 8,214 European ancestry individuals NA Affymetrix [15428572] (imputed) 7 6-bromotryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800099 GCST90200201 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Delta-CEHC levels 6,233 European ancestry individuals NA Affymetrix [15337272] (imputed) 1 delta-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800174 GCST90200202 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetoylcarnitine levels 7,777 European ancestry individuals NA Affymetrix [15414860] (imputed) 5 indoleacetoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800106 GCST90200203 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl leucine levels 7,646 European ancestry individuals NA Affymetrix [15405977] (imputed) 0 N-acetyl-l-leucine measurement http://www.ebi.ac.uk/efo/EFO_0021653 GCST90200204 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoleglyoxylic acid levels 7,848 European ancestry individuals NA Affymetrix [15417670] (imputed) 2 3-indoleglyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801027 GCST90200205 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (1) levels 7,021 European ancestry individuals NA Affymetrix [15382653] (imputed) 1 sulfate of piperine metabolite C18H21NO3 (1) measurement http://www.ebi.ac.uk/efo/EFO_0801036 GCST90200206 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholic acid sulfate (1) levels 6,622 European ancestry individuals NA Affymetrix [15359645] (imputed) 2 glycoursodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800578 GCST90200221 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydrocaffeate sulfate (2) levels 6,519 European ancestry individuals NA Affymetrix [15353466] (imputed) 0 dihydrocaffeate sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801044 GCST90200222 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylhexanoylglutamine levels 5,576 European ancestry individuals NA Affymetrix [15286614] (imputed) 1 4-methylhexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800576 GCST90200223 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-ketocaprylate levels 8,240 European ancestry individuals NA Affymetrix [15430625] (imputed) 3 2-ketocaprylate measurement http://www.ebi.ac.uk/efo/EFO_0800110 GCST90200224 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-methylpyridine sulfate levels 7,446 European ancestry individuals NA Affymetrix [15395961] (imputed) 0 3-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801052 GCST90200225 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxy-2-methylpyridine sulfate levels 6,977 European ancestry individuals NA Affymetrix [15378125] (imputed) 1 5-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801051 GCST90200226 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ethylcatechol sulfate (2) levels 4,814 European ancestry individuals NA Affymetrix [15451266] (imputed) 0 3-ethylcatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801048 GCST90200227 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoylcarnitine (1) levels 8,227 European ancestry individuals NA Affymetrix [15429814] (imputed) 2 3-hydroxyhexanoylcarnitine (1) measurement http://www.ebi.ac.uk/efo/EFO_0800580 GCST90200228 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,6-dihydroxybenzoic acid levels 8,269 European ancestry individuals NA Affymetrix [15431363] (imputed) 1 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90200229 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ethylcatechol sulfate (1) levels 7,062 European ancestry individuals NA Affymetrix [15379652] (imputed) 0 3-ethylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801047 GCST90200230 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lithocholate sulfate (1) levels 7,891 European ancestry individuals NA Affymetrix [15417601] (imputed) 3 lithocholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800579 GCST90200231 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylcatechol sulfate (1) levels 7,565 European ancestry individuals NA Affymetrix [15403204] (imputed) 0 4-acetylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801049 GCST90200232 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-5-methylthio-4-pentenoate (dmtpa) levels 8,225 European ancestry individuals NA Affymetrix [15429973] (imputed) 1 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90200233 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinoylglycine levels 7,862 European ancestry individuals NA Affymetrix [15414738] (imputed) 1 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90200234 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinoyltaurine levels 7,897 European ancestry individuals NA Affymetrix [15417267] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200235 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Undecenoylcarnitine (C11:1) levels 8,253 European ancestry individuals NA Affymetrix [15430983] (imputed) 6 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90200236 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) levels 8,140 European ancestry individuals NA Affymetrix [15425277] (imputed) 0 palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800591 GCST90200237 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol disulfate levels 8,228 European ancestry individuals NA Affymetrix [15429976] (imputed) 3 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90200238 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienedioate (C14:2-DC) levels 7,857 European ancestry individuals NA Affymetrix [15415310] (imputed) 3 tetradecadienedioate (C14:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800585 GCST90200239 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxy-N6,N6,N6-trimethyllysine levels 8,190 European ancestry individuals NA Affymetrix [15428576] (imputed) 0 hydroxy-N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800112 GCST90200240 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol sulfate levels 8,233 European ancestry individuals NA Affymetrix [15430415] (imputed) 2 pregnenetriol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800586 GCST90200241 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholic acid 3-sulfate levels 7,157 European ancestry individuals NA Affymetrix [15387423] (imputed) 5 taurochenodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800584 GCST90200242 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) levels 8,260 European ancestry individuals NA Affymetrix [15430880] (imputed) 1 hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800583 GCST90200243 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxymethyl-2-furoylcarnitine levels 4,803 European ancestry individuals NA Affymetrix [15451679] (imputed) 0 5-hydroxymethyl-2-furoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0801053 GCST90200244 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenedioate (C20:1-DC) levels 7,861 European ancestry individuals NA Affymetrix [15418723] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200245 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trigonelline levels 8,272 European ancestry individuals NA Affymetrix [15431117] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90199696 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecanedioate levels 8,240 European ancestry individuals NA Affymetrix [15430983] (imputed) 1 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90199697 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylcarnitine (c4) levels 8,243 European ancestry individuals NA Affymetrix [15430355] (imputed) 6 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90199698 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylxanthine levels 8,085 European ancestry individuals NA Affymetrix [15424754] (imputed) 1 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90199699 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxylaurate levels 8,206 European ancestry individuals NA Affymetrix [15428790] (imputed) 1 3-hydroxylaurate measurement http://www.ebi.ac.uk/efo/EFO_0800204 GCST90199700 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyridoxate levels 8,089 European ancestry individuals NA Affymetrix [15426442] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90199701 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyhexanoate levels 7,097 European ancestry individuals NA Affymetrix [15379885] (imputed) 0 5-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800206 GCST90199702 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylvaline levels 8,179 European ancestry individuals NA Affymetrix [15427133] (imputed) 1 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90199703 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxysebacate levels 7,325 European ancestry individuals NA Affymetrix [15395259] (imputed) 2 3-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800205 GCST90199704 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylglycine levels 7,311 European ancestry individuals NA Affymetrix [15389974] (imputed) 2 propionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800207 GCST90199705 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrylglycine levels 6,044 European ancestry individuals NA Affymetrix [15318173] (imputed) 2 butyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800208 GCST90199706 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pro-hydroxy-pro levels 8,208 European ancestry individuals NA Affymetrix [15429393] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90199707 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylcarnitine (c3) levels 8,273 European ancestry individuals NA Affymetrix [15430782] (imputed) 4 propionylcarnitine (C3) measurement http://www.ebi.ac.uk/efo/EFO_0800210 GCST90199708 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adrenate (22:4n6) levels 8,279 European ancestry individuals NA Affymetrix [15431484] (imputed) 1 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90199709 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosatrienoate (22:3n3) levels 6,511 European ancestry individuals NA Affymetrix [15351145] (imputed) 1 blood 13,16,19-Docosatrienoic acid amount http://purl.obolibrary.org/obo/OBA_2050329 GCST90199710 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosadienoate (22:2n6) levels 8,264 European ancestry individuals NA Affymetrix [15431075] (imputed) 0 docosadienoate (22:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800211 GCST90199711 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 8,270 European ancestry individuals NA Affymetrix [15431473] (imputed) 1 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90199712 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate n3 DPA; 22:5n3 levels 8,284 European ancestry individuals NA Affymetrix [15431726] (imputed) 1 docosapentaenoate n3 DPA; 22:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021048 GCST90199713 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-ethylpropionate levels 8,238 European ancestry individuals NA Affymetrix [15430961] (imputed) 2 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90199714 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristoleate (14:1n5) levels 8,255 European ancestry individuals NA Affymetrix [15430947] (imputed) 0 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90199715 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-undecenoate (11:1n1) levels 8,243 European ancestry individuals NA Affymetrix [15430792] (imputed) 1 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90199716 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-4-imidazoleacetate levels 8,090 European ancestry individuals NA Affymetrix [15426269] (imputed) 2 1-methyl-4-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800015 GCST90199717 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sebacate (C10-DC) levels 7,926 European ancestry individuals NA Affymetrix [15418507] (imputed) 2 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90199718 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tauro-beta-muricholate levels 4,661 European ancestry individuals NA Affymetrix [15455462] (imputed) 1 tauro-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800213 GCST90199719 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octanoylcarnitine (c8) levels 8,226 European ancestry individuals NA Affymetrix [15428886] (imputed) 4 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90199720 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (3) levels 7,650 European ancestry individuals NA Affymetrix [15402965] (imputed) 1 carotene diol (3) measurement http://www.ebi.ac.uk/efo/EFO_0800172 GCST90200157 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoleoylcarnitine levels 7,532 European ancestry individuals NA Affymetrix [15401806] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200158 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecenedioate (C12:1-DC) levels 8,217 European ancestry individuals NA Affymetrix [15430050] (imputed) 2 dodecenedioate (C12:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800561 GCST90200159 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-2-hexenoylglycine levels 6,545 European ancestry individuals NA Affymetrix [15350543] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200160 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyarachidate levels 8,170 European ancestry individuals NA Affymetrix [15428087] (imputed) 0 2-hydroxyarachidate measurement http://www.ebi.ac.uk/efo/EFO_0800558 GCST90200161 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyphenylacetoylglutamine levels 5,371 European ancestry individuals NA Affymetrix [15273995] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200162 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Heptenedioate (C7:1-DC) levels 8,128 European ancestry individuals NA Affymetrix [15426621] (imputed) 0 heptenedioate (C7:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800564 GCST90200163 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecenedioate (C16:1-DC) levels 8,248 European ancestry individuals NA Affymetrix [15431113] (imputed) 2 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90200164 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioate (C18:1-DC) levels 8,267 European ancestry individuals NA Affymetrix [15431706] (imputed) 3 octadecenedioate (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800563 GCST90200165 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulic acid sulfate levels 5,188 European ancestry individuals NA Affymetrix [15256209] (imputed) 0 dihydroferulic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801026 GCST90200166 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C7H12O2 levels 7,881 European ancestry individuals NA Affymetrix [15417029] (imputed) 1 glutamine conjugate of C7H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800656 GCST90200167 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxyasparagine levels 8,206 European ancestry individuals NA Affymetrix [15430484] (imputed) 0 hydroxyasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800092 GCST90200168 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/14:0, d16:1/15:0) levels 8,267 European ancestry individuals NA Affymetrix [15431894] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200169 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecadienedioate (C18:2-DC) levels 8,231 European ancestry individuals NA Affymetrix [15430442] (imputed) 3 octadecadienedioate (C18:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800565 GCST90200170 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanoate (PFOA) levels 8,199 European ancestry individuals NA Affymetrix [15428812] (imputed) 0 perfluorooctanoate (PFOA) measurement http://www.ebi.ac.uk/efo/EFO_0801024 GCST90200171 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) levels 8,234 European ancestry individuals NA Affymetrix [15430437] (imputed) 3 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) measurement http://www.ebi.ac.uk/efo/EFO_0800566 GCST90200172 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (2) levels 8,233 European ancestry individuals NA Affymetrix [15430437] (imputed) 1 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90200173 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxybutyroylglycine levels 8,171 European ancestry individuals NA Affymetrix [15428349] (imputed) 3 3-hydroxybutyroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800568 GCST90200174 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H14O2 (1) levels 8,128 European ancestry individuals NA Affymetrix [15426648] (imputed) 3 glycine conjugate of C10H14O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800655 GCST90200175 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (1) levels 7,980 European ancestry individuals NA Affymetrix [15422529] (imputed) 1 glutamine conjugate of C6H10O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800657 GCST90200176 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylhydroxyproline levels 6,902 European ancestry individuals NA Affymetrix [15371115] (imputed) 0 N-methylhydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800093 GCST90200177 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C10H18O2 (7) levels 6,090 European ancestry individuals NA Affymetrix [15330067] (imputed) 0 glucuronide of C10H18O2 (7) measurement http://www.ebi.ac.uk/efo/EFO_0800652 GCST90200178 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glyco-beta-muricholate levels 7,206 European ancestry individuals NA Affymetrix [15389403] (imputed) 1 glyco-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800569 GCST90200179 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C12H22O4 (1) levels 5,831 European ancestry individuals NA Affymetrix [15298952] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200180 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,n,n-trimethyl-alanylproline betaine (tmap) levels 8,220 European ancestry individuals NA Affymetrix [15429732] (imputed) 0 N,N,N-trimethyl-alanylproline betaine (TMAP) measurement http://www.ebi.ac.uk/efo/EFO_0800094 GCST90200181 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gentisate levels 8,013 European ancestry individuals NA Affymetrix [15420848] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90199646 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theophylline levels 7,822 European ancestry individuals NA Affymetrix [15416920] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90199647 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,5-anhydroglucitol (1,5-ag) levels 8,139 European ancestry individuals NA Affymetrix [15427754] (imputed) 4 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90199648 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) levels 8,134 European ancestry individuals NA Affymetrix [15425017] (imputed) 6 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800184 GCST90199649 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolelactate levels 8,233 European ancestry individuals NA Affymetrix [15429068] (imputed) 2 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90199650 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoate DHA; 22:6n3 levels 8,279 European ancestry individuals NA Affymetrix [15431754] (imputed) 0 docosahexaenoate DHA; 22:6n3 measurement http://www.ebi.ac.uk/efo/EFO_0021047 GCST90199651 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPS (18:0/18:1) levels 8,055 European ancestry individuals NA Affymetrix [15422153] (imputed) 1 1-stearoyl-2-oleoyl-GPS (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800187 GCST90199652 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-palmitoyl-gpc (14:0/16:0) levels 8,271 European ancestry individuals NA Affymetrix [15431251] (imputed) 0 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800191 GCST90199653 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Paraxanthine levels in elite athletes 7,840 European ancestry individuals NA Affymetrix [15417811] (imputed) 1 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90199654 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methyl-2-oxopentanoate levels 8,255 European ancestry individuals NA Affymetrix [15430745] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90199655 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoxyl sulfate levels 8,242 European ancestry individuals NA Affymetrix [15430680] (imputed) 0 indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010502 GCST90199656 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine 1-phosphate levels 8,246 European ancestry individuals NA Affymetrix [15430743] (imputed) 1 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90199657 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxyisocaproate levels 8,250 European ancestry individuals NA Affymetrix [15430545] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90199658 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPI (18:0) levels 8,260 European ancestry individuals NA Affymetrix [15431436] (imputed) 0 1-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800188 GCST90199659 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dipalmitoyl-gpc (16:0/16:0) levels 8,264 European ancestry individuals NA Affymetrix [15431093] (imputed) 2 1,2-dipalmitoyl-GPC (16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800189 GCST90199660 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maleate levels 8,171 European ancestry individuals NA Affymetrix [15427980] (imputed) 0 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90199661 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerate (i5:0) levels 7,862 European ancestry individuals NA Affymetrix [15416733] (imputed) 0 isovalerate (i5:0) measurement http://www.ebi.ac.uk/efo/EFO_0800010 GCST90199662 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylphenol sulfate levels 7,135 European ancestry individuals NA Affymetrix [15382806] (imputed) 0 4-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800942 GCST90199663 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenyllactate (PLA) levels in elite athletes 8,235 European ancestry individuals NA Affymetrix [15430234] (imputed) 1 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90199664 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylaspartate (naa) levels 8,148 European ancestry individuals NA Affymetrix [15427932] (imputed) 0 N-acetylaspartate (NAA) measurement http://www.ebi.ac.uk/efo/EFO_0800012 GCST90199665 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcarnitine levels (Metabolon platform) 8,256 European ancestry individuals NA Affymetrix [15430703] (imputed) 2 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90199666 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythritol levels in elite athletes 8,167 European ancestry individuals NA Affymetrix [15427701] (imputed) 1 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90199667 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylcarnitine levels (Biocrates platform) 8,242 European ancestry individuals NA Affymetrix [15429420] (imputed) 6 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90199668 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetylcarnitine levels (Biocrates platform) 8,262 European ancestry individuals NA Affymetrix [15430904] (imputed) 2 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90199669 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Iminodiacetate (IDA) levels 8,213 European ancestry individuals NA Affymetrix [15428972] (imputed) 0 iminodiacetate (IDA) measurement http://www.ebi.ac.uk/efo/EFO_0800945 GCST90199670 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine levels 8,192 European ancestry individuals NA Affymetrix [15427953] (imputed) 5 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90199621 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Benzoate levels 7,306 European ancestry individuals NA Affymetrix [15395310] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90199622 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maltotriose levels 4,641 European ancestry individuals NA Affymetrix [15449343] (imputed) 0 maltotriose measurement http://www.ebi.ac.uk/efo/EFO_0800142 GCST90199623 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hippurate levels 8,260 European ancestry individuals NA Affymetrix [15429755] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90199624 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfoxide levels 8,243 European ancestry individuals NA Affymetrix [15430510] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90199625 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xanthurenate levels 7,965 European ancestry individuals NA Affymetrix [15420239] (imputed) 2 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90199626 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-alpha-acetylornithine levels 5,606 European ancestry individuals NA Affymetrix [15291122] (imputed) 1 N-alpha-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800006 GCST90199627 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylhistidine levels 8,289 European ancestry individuals NA Affymetrix [15431449] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90199628 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphorylcholine (GPC) levels 8,212 European ancestry individuals NA Affymetrix [15430145] (imputed) 1 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90199629 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetate levels 7,059 European ancestry individuals NA Affymetrix [15380443] (imputed) 1 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90199630 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxovalerate levels 8,257 European ancestry individuals NA Affymetrix [15431455] (imputed) 0 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90199631 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartarate levels 7,099 European ancestry individuals NA Affymetrix [15375807] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90199632 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Suberate (C8-DC) levels 6,902 European ancestry individuals NA Affymetrix [15376900] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90199633 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxylysine levels 8,128 European ancestry individuals NA Affymetrix [15426861] (imputed) 3 5-hydroxylysine measurement http://www.ebi.ac.uk/efo/EFO_0800002 GCST90199634 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phenylpropionate hydrocinnamate levels 7,925 European ancestry individuals NA Affymetrix [15416781] (imputed) 0 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90199635 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenine levels 8,244 European ancestry individuals NA Affymetrix [15430076] (imputed) 3 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90199636 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglutamate levels 7,802 European ancestry individuals NA Affymetrix [15414233] (imputed) 1 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90199637 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol 3-phosphate levels 8,201 European ancestry individuals NA Affymetrix [15427890] (imputed) 5 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90199638 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole lactate levels 8,256 European ancestry individuals NA Affymetrix [15429719] (imputed) 5 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90199639 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-guanidinobutanoate levels 8,144 European ancestry individuals NA Affymetrix [15428161] (imputed) 2 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90199640 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronate levels 7,988 European ancestry individuals NA Affymetrix [15421888] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90199641 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ribitol levels 8,128 European ancestry individuals NA Affymetrix [15426294] (imputed) 1 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90199642 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycodeoxycholate levels 6,877 European ancestry individuals NA Affymetrix [15372558] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90199643 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theobromine levels 8,137 European ancestry individuals NA Affymetrix [15426624] (imputed) 1 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90199644 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinate levels 8,200 European ancestry individuals NA Affymetrix [15429107] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90199645 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine s-sulfate levels 8,229 European ancestry individuals NA Affymetrix [15429338] (imputed) 0 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90199671 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oxalate (ethanedioate) levels 8,181 European ancestry individuals NA Affymetrix [15427802] (imputed) 1 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90199672 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. DHEAS levels 8,228 European ancestry individuals NA Affymetrix [15430202] (imputed) 2 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90199673 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxymyristate levels 8,235 European ancestry individuals NA Affymetrix [15430577] (imputed) 0 blood 3-hydroxymyristate measurement http://www.ebi.ac.uk/efo/EFO_0022197 GCST90199674 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homoarginine levels 8,265 European ancestry individuals NA Affymetrix [15431411] (imputed) 2 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST90199675 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoylglycerol (18:1) levels 8,225 European ancestry individuals NA Affymetrix [15429515] (imputed) 1 1-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800195 GCST90199676 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxobutyrate levels 8,254 European ancestry individuals NA Affymetrix [15430708] (imputed) 1 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90199677 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartronate (hydroxymalonate) levels 8,125 European ancestry individuals NA Affymetrix [15424666] (imputed) 1 tartronate (hydroxymalonate) measurement http://www.ebi.ac.uk/efo/EFO_0800944 GCST90199678 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxypyridine levels 6,496 European ancestry individuals NA Affymetrix [15348665] (imputed) 0 blood 2,3-dihydroxypyridine measurement http://www.ebi.ac.uk/efo/EFO_0022199 GCST90199679 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoate levels 8,182 European ancestry individuals NA Affymetrix [15429088] (imputed) 1 3-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800193 GCST90199680 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyoctanoate levels 8,224 European ancestry individuals NA Affymetrix [15430073] (imputed) 2 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90199681 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homocitrulline levels 7,998 European ancestry individuals NA Affymetrix [15423374] (imputed) 1 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90199682 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetate levels 8,208 European ancestry individuals NA Affymetrix [15429489] (imputed) 1 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90199683 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoylglycerol (18:2) levels 8,212 European ancestry individuals NA Affymetrix [15429326] (imputed) 0 1-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800199 GCST90199684 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-linoleoylglycerol (18:2) levels 6,378 European ancestry individuals NA Affymetrix [15347823] (imputed) 0 2-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800197 GCST90199685 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolepropionate levels 8,153 European ancestry individuals NA Affymetrix [15426301] (imputed) 2 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90199686 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonate levels 8,151 European ancestry individuals NA Affymetrix [15426652] (imputed) 1 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90199687 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglycine levels 8,250 European ancestry individuals NA Affymetrix [15431220] (imputed) 2 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90199688 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate levels 7,158 European ancestry individuals NA Affymetrix [15388423] (imputed) 0 glycolithocholate measurement http://www.ebi.ac.uk/efo/EFO_0800203 GCST90199689 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. EDTA levels 8,239 European ancestry individuals NA Affymetrix [15430885] (imputed) 0 EDTA measurement http://www.ebi.ac.uk/efo/EFO_0800946 GCST90199690 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylhistidine levels 8,226 European ancestry individuals NA Affymetrix [15430658] (imputed) 2 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90199691 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citramalate levels 7,125 European ancestry individuals NA Affymetrix [15380674] (imputed) 0 blood citramalate measurement http://www.ebi.ac.uk/efo/EFO_0022198 GCST90199692 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoate levels 8,239 European ancestry individuals NA Affymetrix [15430671] (imputed) 1 3-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800198 GCST90199693 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3-dimethylurate levels 7,444 European ancestry individuals NA Affymetrix [15400140] (imputed) 1 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90199694 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Galactonate levels 7,518 European ancestry individuals NA Affymetrix [15401807] (imputed) 1 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90199695 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearidonate (18:4n3) levels 8,240 European ancestry individuals NA Affymetrix [15430435] (imputed) 1 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90199721 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decanoylcarnitine (C10) levels 8,225 European ancestry individuals NA Affymetrix [15429753] (imputed) 3 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90199722 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-dodecenoate (12:1n7) levels 8,248 European ancestry individuals NA Affymetrix [15430644] (imputed) 0 5-dodecenoate 12:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021100 GCST90199723 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylisoleucine levels 7,223 European ancestry individuals NA Affymetrix [15387915] (imputed) 0 N-acetylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800021 GCST90199724 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Campesterol levels 5,300 European ancestry individuals NA Affymetrix [15266412] (imputed) 3 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90199725 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylthreonine levels 8,223 European ancestry individuals NA Affymetrix [15429508] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90199726 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPC (18:1) levels 8,257 European ancestry individuals NA Affymetrix [15431353] (imputed) 1 1-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800218 GCST90199727 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-nonadecenoate (19:1n9) levels 8,277 European ancestry individuals NA Affymetrix [15431871] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90199728 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Piperine levels 8,155 European ancestry individuals NA Affymetrix [15427074] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90199729 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14 levels 8,241 European ancestry individuals NA Affymetrix [15430473] (imputed) 1 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90199730 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-heptadecenoate (17:1n7) levels 8,282 European ancestry individuals NA Affymetrix [15431756] (imputed) 0 10-heptadecenoate 17:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021060 GCST90199731 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl vanillate sulfate levels 4,303 European ancestry individuals NA Affymetrix [15441368] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200207 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (4) levels 7,833 European ancestry individuals NA Affymetrix [15416731] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90200208 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (3) levels 7,705 European ancestry individuals NA Affymetrix [15411825] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90200209 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (2) levels 7,950 European ancestry individuals NA Affymetrix [15420902] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90200210 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxypyridine glucuronide levels 5,882 European ancestry individuals NA Affymetrix [15303944] (imputed) 0 3-hydroxypyridine glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0801043 GCST90200211 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (5) levels 6,582 European ancestry individuals NA Affymetrix [15359661] (imputed) 1 glucuronide of piperine metabolite C17H21NO3 (5) measurement http://www.ebi.ac.uk/efo/EFO_0801033 GCST90200212 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-naphthol sulfate levels 7,673 European ancestry individuals NA Affymetrix [15410689] (imputed) 0 2-naphthol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801038 GCST90200213 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyandrosterone glucuronide levels 8,081 European ancestry individuals NA Affymetrix [15422948] (imputed) 4 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90200214 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylcatechol sulfate levels 8,222 European ancestry individuals NA Affymetrix [15428487] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90200215 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (3) levels 7,006 European ancestry individuals NA Affymetrix [15381980] (imputed) 1 sulfate of piperine metabolite C18H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801037 GCST90200216 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (2,4 or 2,5)-dimethylphenol sulfate levels 5,189 European ancestry individuals NA Affymetrix [15257694] (imputed) 0 (2,4 or 2,5)-dimethylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801039 GCST90200217 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyetiocholanolone glucuronide levels 7,220 European ancestry individuals NA Affymetrix [15385376] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200218 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholic acid glucuronide levels 4,414 European ancestry individuals NA Affymetrix [15438562] (imputed) 1 cholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800574 GCST90200219 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylcatechol sulfate levels 8,139 European ancestry individuals NA Affymetrix [15426802] (imputed) 0 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90200220 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol disulfate levels 106 South Asian ancestry individuals NA Affymetrix [4411206] (imputed) 0 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90203672 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 pregnenetriol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800586 GCST90203673 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholic acid 3-sulfate levels 94 South Asian ancestry individuals NA Affymetrix [4454357] (imputed) 0 taurochenodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800584 GCST90203674 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinoylglycine levels 96 South Asian ancestry individuals NA Affymetrix [4422400] (imputed) 0 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90203675 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Levulinoylcarnitine levels 88 South Asian ancestry individuals NA Affymetrix [4376175] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203676 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoylcarnitine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-hydroxydecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800590 GCST90203677 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Undecenoylcarnitine (C11:1) levels 107 South Asian ancestry individuals NA Affymetrix [4396325] (imputed) 0 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90203678 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) levels 104 South Asian ancestry individuals NA Affymetrix [4448238] (imputed) 0 palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800591 GCST90203679 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,5-dichloro-2,6-dihydroxybenzoic acid levels 106 South Asian ancestry individuals NA Affymetrix [4413715] (imputed) 0 3,5-dichloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801054 GCST90203680 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinoyltaurine levels 102 South Asian ancestry individuals NA Affymetrix [4494791] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203681 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-carboxyethylcysteine levels 106 South Asian ancestry individuals NA Affymetrix [4410350] (imputed) 0 L-Cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021614 GCST90203682 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic acid glycine levels 87 South Asian ancestry individuals NA Affymetrix [4384578] (imputed) 0 vanillic acid glycine measurement http://www.ebi.ac.uk/efo/EFO_0801056 GCST90203683 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (2 or 3)-decenoate (10:1n7 or n8) levels 105 South Asian ancestry individuals NA Affymetrix [4428828] (imputed) 0 (2 or 3)-decenoate (10:1n7 or n8) measurement http://www.ebi.ac.uk/efo/EFO_0800594 GCST90203684 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxy-4-(methylthio)butanoic acid levels 107 South Asian ancestry individuals NA Affymetrix [4391933] (imputed) 0 2-hydroxy-4-(methylthio)butanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800113 GCST90203685 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Metabolonic lactone sulfate levels 106 South Asian ancestry individuals NA Affymetrix [4412931] (imputed) 0 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90203686 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched chain 14:0 dicarboxylic acid levels 104 South Asian ancestry individuals NA Affymetrix [4449471] (imputed) 0 branched chain 14:0 dicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0800593 GCST90203687 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-a-amino-omega-caprolactam levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 (S)-a-amino-omega-caprolactam measurement http://www.ebi.ac.uk/efo/EFO_0801055 GCST90203688 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentose acid levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 pentose acid measurement http://www.ebi.ac.uk/efo/EFO_0800660 GCST90203689 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dibutyl sulfosuccinate levels 107 South Asian ancestry individuals NA Affymetrix [4394305] (imputed) 0 blood dibutyl sulfosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0022212 GCST90203690 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis 3,4-methyleneheptanoate levels 107 South Asian ancestry individuals NA Affymetrix [4396325] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90203691 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-bromo-5-chloro-2,6-dihydroxybenzoic acid levels 98 South Asian ancestry individuals NA Affymetrix [4373091] (imputed) 0 3-bromo-5-chloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801058 GCST90203692 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylcarnitine levels 107 South Asian ancestry individuals NA Affymetrix [4396325] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203693 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0800662 GCST90203694 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,4-di-tert-butylphenol levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 blood 2,4-di-tert-butylphenol measurement http://www.ebi.ac.uk/efo/EFO_0022221 GCST90203695 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decadienedioic acid (C10:2-DC) levels 104 South Asian ancestry individuals NA Affymetrix [4448433] (imputed) 0 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90203696 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9,10-DiHOME levels 98 South Asian ancestry individuals NA Affymetrix [4366388] (imputed) 0 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90203772 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurodeoxycholate levels 74 South Asian ancestry individuals NA Affymetrix [4453260] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90203773 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholate levels 106 South Asian ancestry individuals NA Affymetrix [4412811] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90203774 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinolinate levels 106 South Asian ancestry individuals NA Affymetrix [4417544] (imputed) 0 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90203775 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleate (18:2n6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90203776 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholic acid levels 102 South Asian ancestry individuals NA Affymetrix [4493043] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90203777 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,n6,n6-trimethyllysine levels 107 South Asian ancestry individuals NA Affymetrix [4393856] (imputed) 0 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90203778 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylputrescine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90203779 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosapentaenoate (EPA; 20:5n3) levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 eicosapentaenoate (EPA; 20:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800616 GCST90203780 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylmalonate levels 106 South Asian ancestry individuals NA Affymetrix [4410631] (imputed) 0 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90203781 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 Adenosine 5'-monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0021574 GCST90203782 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyhippurate (salicylurate) levels 106 South Asian ancestry individuals NA Affymetrix [4406169] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90203783 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinate levels 102 South Asian ancestry individuals NA Affymetrix [4485462] (imputed) 0 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90203784 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 3',5'-cyclic monophosphate (camp) levels 81 South Asian ancestry individuals NA Affymetrix [4512157] (imputed) 0 cyclic adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010473 GCST90203785 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methylthioadenosine (mta) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90203786 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,Z or Z,E) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201244 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Chiro-inositol levels 31 African ancestry individuals NA Affymetrix [7845379] (imputed) 0 chiro-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800270 GCST90201245 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17beta-diol disulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90201246 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycosyl-N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800275 GCST90201247 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20alpha-diol disulfate levels 59 African ancestry individuals NA Affymetrix [7495100] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90201248 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotenoid levels (cryptoxanthin) 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 cryptoxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007897 GCST90201249 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) disulfate (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 androstenediol (3beta,17beta) disulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800278 GCST90201250 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800272 GCST90201251 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylphenol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90201252 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylproline levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90201253 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxyisocaproate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90202088 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methyl-2-oxopentanoate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90202089 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoate DHA; 22:6n3 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 docosahexaenoate DHA; 22:6n3 measurement http://www.ebi.ac.uk/efo/EFO_0021047 GCST90202090 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine 1-phosphate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90202091 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyoctanoate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90202092 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoxyl sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300629] (imputed) 0 indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010502 GCST90202093 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPS (18:0/18:1) levels 101 East Asian ancestry individuals NA Affymetrix [4332983] (imputed) 0 1-stearoyl-2-oleoyl-GPS (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800187 GCST90202094 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maleate levels 101 East Asian ancestry individuals NA Affymetrix [4335498] (imputed) 0 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90202095 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Paraxanthine levels in elite athletes 93 East Asian ancestry individuals NA Affymetrix [4308027] (imputed) 0 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90202096 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoate levels 103 East Asian ancestry individuals NA Affymetrix [4299197] (imputed) 0 3-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800193 GCST90202097 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythritol levels in elite athletes 103 East Asian ancestry individuals NA Affymetrix [4299161] (imputed) 0 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90202098 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenyllactate (PLA) levels in elite athletes 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90202099 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylcarnitine levels (Biocrates platform) 102 East Asian ancestry individuals NA Affymetrix [4319918] (imputed) 0 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90202100 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcarnitine levels (Metabolon platform) 103 East Asian ancestry individuals NA Affymetrix [4302395] (imputed) 0 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90202101 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylaspartate (naa) levels 101 East Asian ancestry individuals NA Affymetrix [4333302] (imputed) 0 N-acetylaspartate (NAA) measurement http://www.ebi.ac.uk/efo/EFO_0800012 GCST90202102 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetylcarnitine levels (Biocrates platform) 102 East Asian ancestry individuals NA Affymetrix [4317556] (imputed) 0 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90202103 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine s-sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4297670] (imputed) 0 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90202104 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartronate (hydroxymalonate) levels 102 East Asian ancestry individuals NA Affymetrix [4317409] (imputed) 0 tartronate (hydroxymalonate) measurement http://www.ebi.ac.uk/efo/EFO_0800944 GCST90202105 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxypyridine levels 69 East Asian ancestry individuals NA Affymetrix [4190621] (imputed) 0 blood 2,3-dihydroxypyridine measurement http://www.ebi.ac.uk/efo/EFO_0022199 GCST90202106 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oxalate (ethanedioate) levels 102 East Asian ancestry individuals NA Affymetrix [4317409] (imputed) 0 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90202107 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-5-methylthio-4-pentenoate (dmtpa) levels 107 South Asian ancestry individuals NA Affymetrix [4392870] (imputed) 0 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90203667 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-methylpyridine sulfate levels 82 South Asian ancestry individuals NA Affymetrix [4524317] (imputed) 0 3-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801052 GCST90203668 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,6-dihydroxybenzoic acid levels 107 South Asian ancestry individuals NA Affymetrix [4397310] (imputed) 0 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90203669 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenedioate (C20:1-DC) levels 104 South Asian ancestry individuals NA Affymetrix [4442103] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203670 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienedioate (C14:2-DC) levels 93 South Asian ancestry individuals NA Affymetrix [4477947] (imputed) 0 tetradecadienedioate (C14:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800585 GCST90203671 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ribitol levels 102 East Asian ancestry individuals NA Affymetrix [4315783] (imputed) 0 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90202063 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phenylpropionate hydrocinnamate levels 102 East Asian ancestry individuals NA Affymetrix [4316071] (imputed) 0 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90202064 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartarate levels 82 East Asian ancestry individuals NA Affymetrix [4315563] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90202065 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxovalerate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90202066 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycodeoxycholate levels 71 East Asian ancestry individuals NA Affymetrix [4344522] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90202067 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfoxide levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90202068 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole lactate levels 102 East Asian ancestry individuals NA Affymetrix [4317235] (imputed) 0 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90202069 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetate levels 82 East Asian ancestry individuals NA Affymetrix [4343265] (imputed) 0 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90202070 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xanthurenate levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90202071 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-guanidinobutanoate levels 103 East Asian ancestry individuals NA Affymetrix [4301844] (imputed) 0 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90202072 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphorylcholine (GPC) levels 103 East Asian ancestry individuals NA Affymetrix [4301041] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90202073 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hippurate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90202074 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxylysine levels 100 East Asian ancestry individuals NA Affymetrix [4349366] (imputed) 0 5-hydroxylysine measurement http://www.ebi.ac.uk/efo/EFO_0800002 GCST90202075 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol 3-phosphate levels 102 East Asian ancestry individuals NA Affymetrix [4318649] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90202076 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theophylline levels 91 East Asian ancestry individuals NA Affymetrix [4340563] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90202077 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinate levels 102 East Asian ancestry individuals NA Affymetrix [4322138] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90202078 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theobromine levels 100 East Asian ancestry individuals NA Affymetrix [4358247] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90202079 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerate (i5:0) levels 98 East Asian ancestry individuals NA Affymetrix [4204341] (imputed) 0 isovalerate (i5:0) measurement http://www.ebi.ac.uk/efo/EFO_0800010 GCST90202080 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gentisate levels 96 East Asian ancestry individuals NA Affymetrix [4245900] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90202081 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-palmitoyl-gpc (14:0/16:0) levels 103 East Asian ancestry individuals NA Affymetrix [4302950] (imputed) 0 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800191 GCST90202082 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylphenol sulfate levels 95 East Asian ancestry individuals NA Affymetrix [4267896] (imputed) 0 4-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800942 GCST90202083 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolelactate levels 103 East Asian ancestry individuals NA Affymetrix [4300166] (imputed) 0 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90202084 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dipalmitoyl-gpc (16:0/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1,2-dipalmitoyl-GPC (16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800189 GCST90202085 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPI (18:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800188 GCST90202086 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800184 GCST90202087 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sarcosine levels 107 South Asian ancestry individuals NA Affymetrix [4389336] (imputed) 0 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90203722 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerate levels 106 South Asian ancestry individuals NA Affymetrix [4412969] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90203723 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylleucine levels 101 South Asian ancestry individuals NA Affymetrix [4515582] (imputed) 0 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90203724 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ureidopropionate levels 103 South Asian ancestry individuals NA Affymetrix [4476430] (imputed) 0 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90203725 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylmethionine levels 103 South Asian ancestry individuals NA Affymetrix [4466135] (imputed) 0 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90203726 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thyroxine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90203727 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylvaline levels 105 South Asian ancestry individuals NA Affymetrix [4426039] (imputed) 0 N-acetylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800117 GCST90203728 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (z,z) levels 107 South Asian ancestry individuals NA Affymetrix [4389201] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203729 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erucate (22:1n9) levels 106 South Asian ancestry individuals NA Affymetrix [4406631] (imputed) 0 erucate (22:1n9) measurement http://www.ebi.ac.uk/efo/EFO_0800601 GCST90203730 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetamidobutanoate levels 105 South Asian ancestry individuals NA Affymetrix [4430555] (imputed) 0 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90203731 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltyrosine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90203732 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-alanine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90203733 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-tocopherol levels 107 South Asian ancestry individuals NA Affymetrix [4391565] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90203734 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-aminoisobutyrate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90203735 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyisobutyrate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90203736 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrate levels 107 South Asian ancestry individuals NA Affymetrix [4390541] (imputed) 0 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90203737 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90203738 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamine levels 107 South Asian ancestry individuals NA Affymetrix [4394255] (imputed) 0 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90203739 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminobutyrate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90203740 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-3-methylglutarate levels 106 South Asian ancestry individuals NA Affymetrix [4414371] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90203741 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl ethanolamide levels 106 South Asian ancestry individuals NA Affymetrix [4405754] (imputed) 0 oleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800604 GCST90203742 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ursodeoxycholate levels 100 South Asian ancestry individuals NA Affymetrix [4522806] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90203743 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylpyruvate levels 103 South Asian ancestry individuals NA Affymetrix [4464542] (imputed) 0 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90203744 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homovanillate (hva) levels 77 South Asian ancestry individuals NA Affymetrix [4376742] (imputed) 0 HVA measurement http://www.ebi.ac.uk/efo/EFO_0005131 GCST90203745 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylneuraminate levels 106 South Asian ancestry individuals NA Affymetrix [4410630] (imputed) 0 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90203746 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrate/isobutyrate (4:0) levels 105 South Asian ancestry individuals NA Affymetrix [4438259] (imputed) 0 isobutyrate (4:0) measurement http://www.ebi.ac.uk/efo/EFO_0800605 GCST90203747 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosaminylasparagine levels 106 South Asian ancestry individuals NA Affymetrix [4413564] (imputed) 0 N-acetylglucosaminylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800151 GCST90203748 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetoacetate levels 81 South Asian ancestry individuals NA Affymetrix [4535327] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90203749 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linoleate (20:2n6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90203750 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatine levels 107 South Asian ancestry individuals NA Affymetrix [4396465] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90203751 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cys-gly, oxidized levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90203752 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylhistidine levels 106 South Asian ancestry individuals NA Affymetrix [4415233] (imputed) 0 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90203753 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxystearate levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90203754 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phosphoglycerate levels 107 South Asian ancestry individuals NA Affymetrix [4396325] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90203755 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylleucine levels 105 South Asian ancestry individuals NA Affymetrix [4421194] (imputed) 0 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90203756 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Choline levels 107 South Asian ancestry individuals NA Affymetrix [4392767] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90203757 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N1-methyladenosine levels 107 South Asian ancestry individuals NA Affymetrix [4397381] (imputed) 0 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90203758 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Anthranilate levels 71 South Asian ancestry individuals NA Affymetrix [4531509] (imputed) 0 anthranilate measurement http://www.ebi.ac.uk/efo/EFO_0800123 GCST90203759 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxytyrosine levels 106 South Asian ancestry individuals NA Affymetrix [4414822] (imputed) 0 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90203760 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovalerate levels 106 South Asian ancestry individuals NA Affymetrix [4416858] (imputed) 0 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90203761 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800608 GCST90203762 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels 104 South Asian ancestry individuals NA Affymetrix [4452811] (imputed) 0 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800609 GCST90203763 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetate levels 103 South Asian ancestry individuals NA Affymetrix [4471743] (imputed) 0 4-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800124 GCST90203764 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90203765 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoyl sphingomyelin (d18:1/18:0) levels 107 South Asian ancestry individuals NA Affymetrix [4388259] (imputed) 0 stearoyl sphingomyelin (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800611 GCST90203766 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingosine (d18:1/18:0) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800613 GCST90203767 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5,6-dihydrothymine levels 106 South Asian ancestry individuals NA Affymetrix [4409572] (imputed) 0 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90203768 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate levels 106 South Asian ancestry individuals NA Affymetrix [4412811] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90203769 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-gpc (16:0/18:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90203770 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-gpc (16:0/18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90203771 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol disulfate (C21H34O8S2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 pregnenediol disulfate (C21H34O8S2) measurement http://www.ebi.ac.uk/efo/EFO_0800279 GCST90201254 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 21-hydroxypregnenolone disulfate levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90201255 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17alpha-diol monosulfate levels 36 African ancestry individuals NA Affymetrix [7529767] (imputed) 0 5alpha-androstan-3alpha,17alpha-diol monosulfate measurement http://www.ebi.ac.uk/efo/EFO_0800283 GCST90201256 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinylcarnitine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90201257 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels 56 African ancestry individuals NA Affymetrix [7570705] (imputed) 0 5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800284 GCST90201258 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) disulfate (2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 androstenediol (3beta,17beta) disulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800280 GCST90201259 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-diol disulfate levels 30 African ancestry individuals NA Affymetrix [7132608] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90201260 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17alpha-diol disulfate levels 50 African ancestry individuals NA Affymetrix [7448549] (imputed) 0 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90201261 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) levels 58 African ancestry individuals NA Affymetrix [7514512] (imputed) 0 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800285 GCST90201262 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol disulfate levels 44 African ancestry individuals NA Affymetrix [7605221] (imputed) 0 5alpha-androstan-3alpha,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800287 GCST90201263 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) monosulfate (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 androstenediol (3beta,17beta) monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800294 GCST90201264 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800288 GCST90201265 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels 54 African ancestry individuals NA Affymetrix [7688219] (imputed) 0 5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800291 GCST90201266 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol sulfate (C21H34O5S) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 pregnenediol sulfate (C21H34O5S) measurement http://www.ebi.ac.uk/efo/EFO_0800299 GCST90201267 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxycoumarin levels 48 African ancestry individuals NA Affymetrix [7383240] (imputed) 0 4-hydroxycoumarin measurement http://www.ebi.ac.uk/efo/EFO_0800959 GCST90201268 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3alpha, 17alpha) monosulfate (3) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 androstenediol (3alpha, 17alpha) monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0800293 GCST90201269 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) monosulfate (2) levels 56 African ancestry individuals NA Affymetrix [7559010] (imputed) 0 androstenediol (3beta,17beta) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800295 GCST90201270 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 16a-hydroxy DHEA 3-sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90201271 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenolone sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 pregnenolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800303 GCST90201272 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyhippurate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90201273 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl sphingomyelin (d18:1/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90201274 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-beta-alanine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90201275 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/18:1, d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0022108 GCST90201276 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90201277 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Andro steroid monosulfate C19H28O6S (1) levels 54 African ancestry individuals NA Affymetrix [7691000] (imputed) 0 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90201278 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid 12-sulfate levels 81 South Asian ancestry individuals NA Affymetrix [4523285] (imputed) 0 deoxycholic acid (12 or 24)-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800599 GCST90203697 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (2) levels 76 South Asian ancestry individuals NA Affymetrix [4379640] (imputed) 0 2-methoxyhydroquinone sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801062 GCST90203698 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminoadipate levels 101 South Asian ancestry individuals NA Affymetrix [4509256] (imputed) 0 blood N-acetyl-2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0022202 GCST90203699 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (1) levels 92 South Asian ancestry individuals NA Affymetrix [4492495] (imputed) 0 2-methoxyhydroquinone sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801061 GCST90203700 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylglycine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203701 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (3) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203702 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203703 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (1) levels 106 South Asian ancestry individuals NA Affymetrix [4407862] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203704 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (2) levels 107 South Asian ancestry individuals NA Affymetrix [4392662] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203705 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (1) levels 101 South Asian ancestry individuals NA Affymetrix [4510425] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203706 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203707 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (2) levels 107 South Asian ancestry individuals NA Affymetrix [4389201] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203708 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203709 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203710 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetrahydrocortisol glucuronide levels 105 South Asian ancestry individuals NA Affymetrix [4433719] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203711 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (3) levels 103 South Asian ancestry individuals NA Affymetrix [4472921] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203712 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (4) levels 106 South Asian ancestry individuals NA Affymetrix [4410817] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203713 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-4-hydroxyproline levels 107 South Asian ancestry individuals NA Affymetrix [4392870] (imputed) 0 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90203714 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-oxoproline levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90203715 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Allantoin levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90203716 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xanthine levels 105 South Asian ancestry individuals NA Affymetrix [4429321] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90203717 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pipecolate levels 107 South Asian ancestry individuals NA Affymetrix [4390626] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90203718 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantothenate levels 106 South Asian ancestry individuals NA Affymetrix [4415427] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90203719 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinate levels 86 South Asian ancestry individuals NA Affymetrix [4403505] (imputed) 0 picolinate measurement http://www.ebi.ac.uk/efo/EFO_0800115 GCST90203720 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphoethanolamine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90203721 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25422 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-25422 measurement http://www.ebi.ac.uk/efo/EFO_0800927 GCST90202038 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25343 levels 59 African ancestry individuals NA Affymetrix [7546954] (imputed) 0 X-25343 measurement http://www.ebi.ac.uk/efo/EFO_0800922 GCST90202039 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24949 levels 52 African ancestry individuals NA Affymetrix [7726422] (imputed) 0 X-24949 measurement http://www.ebi.ac.uk/efo/EFO_0800911 GCST90202040 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24951 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-24951 measurement http://www.ebi.ac.uk/efo/EFO_0800912 GCST90202041 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24947 levels 54 African ancestry individuals NA Affymetrix [7807081] (imputed) 0 X-24947 measurement http://www.ebi.ac.uk/efo/EFO_0800910 GCST90202042 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24812 levels 52 African ancestry individuals NA Affymetrix [7703707] (imputed) 0 X-24812 measurement http://www.ebi.ac.uk/efo/EFO_0800908 GCST90202043 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25265 levels 57 African ancestry individuals NA Affymetrix [7527108] (imputed) 0 X-25265 measurement http://www.ebi.ac.uk/efo/EFO_0800917 GCST90202044 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26054 levels 59 African ancestry individuals NA Affymetrix [7499364] (imputed) 0 X-26054 measurement http://www.ebi.ac.uk/efo/EFO_0800939 GCST90202045 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25828 levels 58 African ancestry individuals NA Affymetrix [7525851] (imputed) 0 X-25828 measurement http://www.ebi.ac.uk/efo/EFO_0800936 GCST90202046 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25810 levels 59 African ancestry individuals NA Affymetrix [7498842] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202047 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25790 levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 X-25790 measurement http://www.ebi.ac.uk/efo/EFO_0800933 GCST90202048 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25520 levels 58 African ancestry individuals NA Affymetrix [7526130] (imputed) 0 X-25520 measurement http://www.ebi.ac.uk/efo/EFO_0800931 GCST90202049 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25957 levels 53 African ancestry individuals NA Affymetrix [7804655] (imputed) 0 X-25957 measurement http://www.ebi.ac.uk/efo/EFO_0800938 GCST90202050 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26111 levels 55 African ancestry individuals NA Affymetrix [7698458] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202051 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25519 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-25519 measurement http://www.ebi.ac.uk/efo/EFO_0800930 GCST90202052 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25433 levels 49 African ancestry individuals NA Affymetrix [7580479] (imputed) 0 X-25433 measurement http://www.ebi.ac.uk/efo/EFO_0800928 GCST90202053 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26109 levels 40 African ancestry individuals NA Affymetrix [7188054] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202054 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine levels 101 East Asian ancestry individuals NA Affymetrix [4325364] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90202055 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Benzoate levels 95 East Asian ancestry individuals NA Affymetrix [4257925] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90202056 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglutamate levels 101 East Asian ancestry individuals NA Affymetrix [4333189] (imputed) 0 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90202057 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronate levels 99 East Asian ancestry individuals NA Affymetrix [4191023] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90202058 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-alpha-acetylornithine levels 67 East Asian ancestry individuals NA Affymetrix [4197100] (imputed) 0 N-alpha-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800006 GCST90202059 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Suberate (C8-DC) levels 87 East Asian ancestry individuals NA Affymetrix [4231570] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90202060 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylhistidine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90202061 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90202062 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_967) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279641 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_968) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279642 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_972) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279643 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_980) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279644 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_981) (2-Chloro-3-oxoadipate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 2-chloro-3-oxoadipate measurement http://www.ebi.ac.uk/efo/EFO_0803473 GCST90279645 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1010) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279646 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1013) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 16 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279647 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1019) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279648 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_102) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279649 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1021) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279650 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1031) (Proline betaine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 proline betaine measurement http://www.ebi.ac.uk/efo/EFO_0011000 GCST90279651 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1033) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279652 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1040) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279653 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1043) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279654 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1069) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279655 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_107) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279656 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1078) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279657 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_108) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279658 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1084) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279659 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1088) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279660 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1101) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279661 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1104) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279662 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5075) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280351 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_508) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280352 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5083) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 116 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280353 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5221) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280379 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5222) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280380 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5233) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280381 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5234) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280382 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5246) ((5Z7E)-(3S)-262626-trifluoro-27-nor-910-seco-5710(19)-cholestatriene-325-diol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 level of (5Z,7E)-(3S)-26,26,26-trifluoro-27-nor-9,10-seco-5,7,10(19)-cholestatriene-3,25-diol in blood serum http://purl.obolibrary.org/obo/OBA_2045037 GCST90280383 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5250) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280384 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5256) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280385 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5260) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280386 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5279) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280387 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5281) (N-(9Z-octadecenoyl)-tyrosine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280388 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_529) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280389 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5290) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280390 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5295) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280391 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5298) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280392 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5299) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280393 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5302) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280394 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5316) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280395 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5325) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280396 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5326) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280397 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5329) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280398 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5330) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280399 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5333) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280400 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_534) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280401 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5341) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280402 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5345) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280403 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5089) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280354 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_509) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280355 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5093) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280356 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5098) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280357 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5099) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280358 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5100) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280359 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5101) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280360 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5103) (Linoleyl carnitine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280361 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5106) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280362 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5113) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280363 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5120) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280364 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5135) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280365 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5137) (Cysteineglutathione disulfide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90280366 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5138) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280367 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5140) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280368 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5144) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280369 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5154) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280370 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5169) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280371 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5170) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280372 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5176) (Istamycin C1) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 istamycin C1 measurement http://www.ebi.ac.uk/efo/EFO_0803502 GCST90280373 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5178) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280374 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5181) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280375 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5189) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280376 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5193) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280377 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5206) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280378 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5562) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279550 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5563) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279551 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5566) (Permetin A) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 permetin A measurement http://www.ebi.ac.uk/efo/EFO_0803446 GCST90279552 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5568) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279553 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5570) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279554 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5571) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279555 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5576) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279556 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5577) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279557 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5578) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279558 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5579) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279559 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5580) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279560 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5583) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279561 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5587) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279562 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5592) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279563 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5594) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279564 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5595) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279565 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5597) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279566 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5598) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279567 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_560) (12-Benzisothiazol-3(2H)-one) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279568 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_564) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279569 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_565) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279570 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_572) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279571 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_584) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279572 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_590) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279573 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_60) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279574 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4710) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280280 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4711) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280281 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4713) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280282 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4715) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280283 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4726) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280284 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4728) (Dibromobisphenol A) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280285 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4743) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280286 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4745) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280287 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4746) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280288 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4752) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280289 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4758) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280290 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4768) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280291 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_751) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279603 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_753) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279604 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_754) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279605 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_760) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279606 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_772) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279607 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_773) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279608 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_779) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279609 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_780) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279610 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_783) (Phenylmethanesulfonyl fluoride) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279611 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_789) (Arginine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90279612 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_793) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279613 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_803) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279614 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_805) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279615 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_718) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279600 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_729) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279601 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_74) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279602 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_417) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280174 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4453) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280234 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4468) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280235 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4474) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280236 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4475) (Guanosine monophosphate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 guanosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010495 GCST90280237 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4476) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280238 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4482) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280239 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4496) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280240 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4497) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280241 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4520) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280242 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4522) (3 5-Tetradecadiencarnitine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280243 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4524) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280244 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4530) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280245 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4531) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280246 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4540) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280247 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4543) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280248 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4544) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280249 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4555) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280250 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4562) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280251 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4566) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280252 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4567) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280253 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4576) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280254 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_807) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279616 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_811) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279617 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_813) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279618 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_815) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279619 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_817) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279620 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_820) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279621 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_823) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279622 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_824) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279623 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_837) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279624 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_839) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279625 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_848) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279626 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_850) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279627 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_852) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279628 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_869) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279629 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_872) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279630 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_88) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279631 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_887) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279632 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_91) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279633 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_919) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279634 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_926) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279635 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_936) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279636 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_937) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279637 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_942) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279638 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_945) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279639 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_960) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279640 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4580) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280255 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4583) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280256 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4585) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280257 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4586) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280258 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4588) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280259 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4589) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280260 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4594) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280261 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_46) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280262 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4602) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280263 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4605) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280264 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4607) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280265 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4615) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280266 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4620) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280267 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4635) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280268 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4640) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280269 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4650) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280270 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4660) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280271 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4661) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280272 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4663) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280273 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4665) (1-Amino-24-dibromoanthraquinone) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 1-amino-24-dibromoanthraquinone measurement http://www.ebi.ac.uk/efo/EFO_0803471 GCST90280274 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4668) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280275 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4701) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280276 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4704) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280277 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4707) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280278 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_471) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280279 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dilinoleoyl-GPE (18:2/18:2) levels 6,804 European ancestry individuals NA Affymetrix [15363737] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200068 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamate levels 6,227 European ancestry individuals NA Affymetrix [15326869] (imputed) 1 phenylacetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800687 GCST90200069 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels 8,083 European ancestry individuals NA Affymetrix [15423320] (imputed) 5 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800464 GCST90200070 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcholine levels 8,209 European ancestry individuals NA Affymetrix [15429651] (imputed) 0 palmitoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800473 GCST90200071 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thioproline levels 8,226 European ancestry individuals NA Affymetrix [15429964] (imputed) 1 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90200072 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) levels 8,063 European ancestry individuals NA Affymetrix [15424604] (imputed) 4 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800450 GCST90200073 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPG (18:2) levels 8,115 European ancestry individuals NA Affymetrix [15425683] (imputed) 2 1-linoleoyl-GPG (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800472 GCST90200074 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (p-16:0/18:2) levels 8,254 European ancestry individuals NA Affymetrix [15431313] (imputed) 2 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800440 GCST90200075 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (p-18:0/18:2) levels 8,261 European ancestry individuals NA Affymetrix [15431332] (imputed) 2 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90200076 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPI (18:0/18:1) levels 8,111 European ancestry individuals NA Affymetrix [15423688] (imputed) 4 1-stearoyl-2-oleoyl-GPI (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800469 GCST90200077 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels 8,264 European ancestry individuals NA Affymetrix [15431143] (imputed) 2 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800453 GCST90200078 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) levels 8,121 European ancestry individuals NA Affymetrix [15426002] (imputed) 6 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800470 GCST90200079 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) levels 8,123 European ancestry individuals NA Affymetrix [15425447] (imputed) 4 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800439 GCST90200080 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) levels 8,267 European ancestry individuals NA Affymetrix [15431184] (imputed) 2 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800449 GCST90200081 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) levels 8,205 European ancestry individuals NA Affymetrix [15428662] (imputed) 4 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800443 GCST90200082 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 8,266 European ancestry individuals NA Affymetrix [15431146] (imputed) 4 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800466 GCST90200083 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcholine levels 8,120 European ancestry individuals NA Affymetrix [15424015] (imputed) 0 oleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800477 GCST90200084 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 8,245 European ancestry individuals NA Affymetrix [15430731] (imputed) 4 glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800476 GCST90200085 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonoylcholine levels 8,170 European ancestry individuals NA Affymetrix [15427542] (imputed) 1 arachidonoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800478 GCST90200086 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methylserine levels 7,722 European ancestry individuals NA Affymetrix [15410215] (imputed) 0 2-methylserine measurement http://www.ebi.ac.uk/efo/EFO_0800087 GCST90200087 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-3-hydroxybutyrylcarnitine levels 8,249 European ancestry individuals NA Affymetrix [15431309] (imputed) 2 (S)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800475 GCST90200088 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinoylcarnitine levels 8,004 European ancestry individuals NA Affymetrix [15419240] (imputed) 6 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200089 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenoyl-choline levels 6,954 European ancestry individuals NA Affymetrix [15372795] (imputed) 0 dihomo-linolenoyl-choline measurement http://www.ebi.ac.uk/efo/EFO_0800481 GCST90200090 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoylcholine levels 7,440 European ancestry individuals NA Affymetrix [15396217] (imputed) 0 docosahexaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800479 GCST90200091 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholate glucuronide (1) levels 4,381 European ancestry individuals NA Affymetrix [15426191] (imputed) 0 glycocholic acid measurement http://www.ebi.ac.uk/efo/EFO_0010492 GCST90200092 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24978 levels 5,151 European ancestry individuals NA Affymetrix [15248599] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200640 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24970 levels 8,263 European ancestry individuals NA Affymetrix [15430626] (imputed) 0 X-24970 measurement http://www.ebi.ac.uk/efo/EFO_0800913 GCST90200641 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24795 levels 4,986 European ancestry individuals NA Affymetrix [15466838] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200642 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24951 levels 8,208 European ancestry individuals NA Affymetrix [15428739] (imputed) 0 X-24951 measurement http://www.ebi.ac.uk/efo/EFO_0800912 GCST90200643 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24728 levels 8,160 European ancestry individuals NA Affymetrix [15427183] (imputed) 0 X-24728 measurement http://www.ebi.ac.uk/efo/EFO_0800903 GCST90200644 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24565 levels 4,364 European ancestry individuals NA Affymetrix [15431669] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200645 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24801 levels 8,059 European ancestry individuals NA Affymetrix [15424806] (imputed) 7 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200646 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24736 levels 4,846 European ancestry individuals NA Affymetrix [15463052] (imputed) 4 X-24736 measurement http://www.ebi.ac.uk/efo/EFO_0800904 GCST90200647 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24585 levels 8,241 European ancestry individuals NA Affymetrix [15430115] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200648 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24588 levels 8,239 European ancestry individuals NA Affymetrix [15430112] (imputed) 9 X-24588 measurement http://www.ebi.ac.uk/efo/EFO_0800898 GCST90200649 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25109 levels 7,477 European ancestry individuals NA Affymetrix [15402359] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200650 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24947 levels 8,002 European ancestry individuals NA Affymetrix [15421195] (imputed) 8 X-24947 measurement http://www.ebi.ac.uk/efo/EFO_0800910 GCST90200651 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24949 levels 7,174 European ancestry individuals NA Affymetrix [15385214] (imputed) 3 X-24949 measurement http://www.ebi.ac.uk/efo/EFO_0800911 GCST90200652 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24812 levels 7,878 European ancestry individuals NA Affymetrix [15414520] (imputed) 1 X-24812 measurement http://www.ebi.ac.uk/efo/EFO_0800908 GCST90200653 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25217 levels 4,098 European ancestry individuals NA Affymetrix [15416837] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200654 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25828 levels 8,156 European ancestry individuals NA Affymetrix [15428691] (imputed) 0 X-25828 measurement http://www.ebi.ac.uk/efo/EFO_0800936 GCST90200655 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25371 levels 8,205 European ancestry individuals NA Affymetrix [15428528] (imputed) 3 X-25371 measurement http://www.ebi.ac.uk/efo/EFO_0800923 GCST90200656 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25419 levels 7,994 European ancestry individuals NA Affymetrix [15423198] (imputed) 1 X-25419 measurement http://www.ebi.ac.uk/efo/EFO_0800925 GCST90200657 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25265 levels 7,916 European ancestry individuals NA Affymetrix [15417809] (imputed) 0 X-25265 measurement http://www.ebi.ac.uk/efo/EFO_0800917 GCST90200658 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25172 levels 8,117 European ancestry individuals NA Affymetrix [15425497] (imputed) 0 X-25172 measurement http://www.ebi.ac.uk/efo/EFO_0800916 GCST90200659 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) levels 8,262 European ancestry individuals NA Affymetrix [15431281] (imputed) 4 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800410 GCST90200063 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphinganine (d18:0/16:0) levels 8,208 European ancestry individuals NA Affymetrix [15428195] (imputed) 0 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90200064 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) levels 8,251 European ancestry individuals NA Affymetrix [15430237] (imputed) 4 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800411 GCST90200065 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-tocopherol/beta-tocopherol levels 8,231 European ancestry individuals NA Affymetrix [15430879] (imputed) 0 beta-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0800168 GCST90200066 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels 8,113 European ancestry individuals NA Affymetrix [15424629] (imputed) 3 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800413 GCST90200067 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90203246 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine-glutathione disulfide levels 100 South Asian ancestry individuals NA Affymetrix [4530175] (imputed) 0 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90203247 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylguanine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90203248 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methyluridine (ribothymidine) levels 107 South Asian ancestry individuals NA Affymetrix [4394543] (imputed) 0 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90203249 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylglycine levels 86 South Asian ancestry individuals NA Affymetrix [4427541] (imputed) 0 isobutyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800029 GCST90203250 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroquinone sulfate levels 97 South Asian ancestry individuals NA Affymetrix [4391077] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90203251 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90203252 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 7-alpha-hydroxy-3-oxo-4-cholestenoate 7-Hoca measurement http://www.ebi.ac.uk/efo/EFO_0021116 GCST90203253 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gulonate levels 95 South Asian ancestry individuals NA Affymetrix [4440597] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90203254 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcitrulline levels 85 South Asian ancestry individuals NA Affymetrix [4457160] (imputed) 0 N-acetylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800028 GCST90203255 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovaleroylcarnitine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 beta-hydroxyisovaleroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800031 GCST90203256 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarylcarnitine (c5-dc) levels 107 South Asian ancestry individuals NA Affymetrix [4392753] (imputed) 0 glutarylcarnitine (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800030 GCST90203257 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecanedioate (C16-DC) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90203258 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPE (18:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800247 GCST90203259 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Catechol sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4391933] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90203260 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate (n6 DPA; 22:5n6) levels 91 South Asian ancestry individuals NA Affymetrix [4507882] (imputed) 0 docosapentaenoate (n6 DPA; 22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800249 GCST90203261 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxypalmitate levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90203262 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C5:1 levels 105 South Asian ancestry individuals NA Affymetrix [4421194] (imputed) 0 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90203263 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecanedioate (C14-DC) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90203264 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-aspartyl-glutamate (naag) levels 102 South Asian ancestry individuals NA Affymetrix [4490661] (imputed) 0 N-acetyl-aspartyl-glutamate (NAAG) measurement http://www.ebi.ac.uk/efo/EFO_0800033 GCST90203265 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonoyl-GPE (20:4n6) levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 1-arachidonoyl-GPE (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800248 GCST90203266 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-palmitoleoyl-GPC (16:1) levels 86 South Asian ancestry individuals NA Affymetrix [4396575] (imputed) 0 2-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800240 GCST90203267 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPE (16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800245 GCST90203268 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPE (18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800246 GCST90203269 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-ribosyl-imidazoleacetate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90203270 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeic acid sulfate levels 7,798 European ancestry individuals NA Affymetrix [15411818] (imputed) 0 caffeic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801013 GCST90200093 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 2-sulfate levels 8,089 European ancestry individuals NA Affymetrix [15424875] (imputed) 1 ascorbic acid 2-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800169 GCST90200094 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) levels 8,188 European ancestry individuals NA Affymetrix [15428679] (imputed) 1 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800483 GCST90200095 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-nonadecenoate (19:1n9) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90203199 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Epiandrosterone sulfate levels 106 South Asian ancestry individuals NA Affymetrix [4408554] (imputed) 0 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90203200 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglycine levels 107 South Asian ancestry individuals NA Affymetrix [4388259] (imputed) 0 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90203201 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylmethionine levels 107 South Asian ancestry individuals NA Affymetrix [4394255] (imputed) 0 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90203202 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythronate levels 107 South Asian ancestry individuals NA Affymetrix [4393796] (imputed) 0 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90203203 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoate (20:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 eicosenoate (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800220 GCST90203204 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4390947] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90203205 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylthreonine levels 106 South Asian ancestry individuals NA Affymetrix [4411461] (imputed) 0 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90203206 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stachydrine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90203207 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltryptophan levels 102 South Asian ancestry individuals NA Affymetrix [4491650] (imputed) 0 gamma-glutamyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800671 GCST90203208 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylproline levels 90 South Asian ancestry individuals NA Affymetrix [4529397] (imputed) 0 blood N-acetylproline measurement http://www.ebi.ac.uk/efo/EFO_0022207 GCST90203209 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenate [alpha or gamma; (18:3n3 or 6)] levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90203210 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Campesterol levels 69 South Asian ancestry individuals NA Affymetrix [4295387] (imputed) 0 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90203211 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPC (18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800218 GCST90203212 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-gpc (18:0) levels 107 South Asian ancestry individuals NA Affymetrix [4395425] (imputed) 0 1-stearoyl-GPC (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800217 GCST90203213 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14 levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90203214 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcarnitine levels 105 South Asian ancestry individuals NA Affymetrix [4429999] (imputed) 0 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90203215 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Laurylcarnitine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90203216 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3,7-trimethylurate levels 98 South Asian ancestry individuals NA Affymetrix [4362460] (imputed) 0 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90203217 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N4-acetylcytidine levels 99 South Asian ancestry individuals NA Affymetrix [4354442] (imputed) 0 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90203218 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,7-dimethyluric acid levels 102 South Asian ancestry individuals NA Affymetrix [4485329] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90203219 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerylcarnitine (C5) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 isovalerylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800024 GCST90203220 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23974 levels 7,752 European ancestry individuals NA Affymetrix [15413226] (imputed) 1 X-23974 measurement http://www.ebi.ac.uk/efo/EFO_0800867 GCST90200615 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23659 levels 8,176 European ancestry individuals NA Affymetrix [15428060] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200616 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23665 levels 8,214 European ancestry individuals NA Affymetrix [15428821] (imputed) 0 X-23665 measurement http://www.ebi.ac.uk/efo/EFO_0800859 GCST90200617 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23782 levels 8,263 European ancestry individuals NA Affymetrix [15431333] (imputed) 0 X-23782 measurement http://www.ebi.ac.uk/efo/EFO_0800865 GCST90200618 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24295 levels 7,987 European ancestry individuals NA Affymetrix [15419388] (imputed) 0 X-24295 measurement http://www.ebi.ac.uk/efo/EFO_0800869 GCST90200619 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24243 levels 7,540 European ancestry individuals NA Affymetrix [15402678] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200620 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23739 levels 8,249 European ancestry individuals NA Affymetrix [15431287] (imputed) 1 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90200621 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23997 levels 7,804 European ancestry individuals NA Affymetrix [15409862] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90200622 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24241 levels 8,053 European ancestry individuals NA Affymetrix [15424531] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200623 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24328 levels 7,807 European ancestry individuals NA Affymetrix [15416793] (imputed) 4 X-24328 measurement http://www.ebi.ac.uk/efo/EFO_0800873 GCST90200624 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24456 levels 6,523 European ancestry individuals NA Affymetrix [15350499] (imputed) 0 X-24456 measurement http://www.ebi.ac.uk/efo/EFO_0800885 GCST90200625 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24418 levels 5,952 European ancestry individuals NA Affymetrix [15310277] (imputed) 5 X-24418 measurement http://www.ebi.ac.uk/efo/EFO_0800879 GCST90200626 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24344 levels 5,457 European ancestry individuals NA Affymetrix [15275870] (imputed) 0 X-24344 measurement http://www.ebi.ac.uk/efo/EFO_0800876 GCST90200627 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24556 levels 8,004 European ancestry individuals NA Affymetrix [15422677] (imputed) 3 X-24556 measurement http://www.ebi.ac.uk/efo/EFO_0800895 GCST90200628 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24337 levels 8,088 European ancestry individuals NA Affymetrix [15423414] (imputed) 2 X-24337 measurement http://www.ebi.ac.uk/efo/EFO_0800875 GCST90200629 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24546 levels 6,391 European ancestry individuals NA Affymetrix [15351111] (imputed) 4 X-24546 measurement http://www.ebi.ac.uk/efo/EFO_0800893 GCST90200630 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24306 levels 8,074 European ancestry individuals NA Affymetrix [15424356] (imputed) 0 X-24306 measurement http://www.ebi.ac.uk/efo/EFO_0800870 GCST90200631 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24307 levels 8,119 European ancestry individuals NA Affymetrix [15426298] (imputed) 0 X-24307 measurement http://www.ebi.ac.uk/efo/EFO_0800871 GCST90200632 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24334 levels 6,975 European ancestry individuals NA Affymetrix [15374286] (imputed) 1 X-24334 measurement http://www.ebi.ac.uk/efo/EFO_0800874 GCST90200633 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24518 levels 6,131 European ancestry individuals NA Affymetrix [15326231] (imputed) 5 X-24518 measurement http://www.ebi.ac.uk/efo/EFO_0800890 GCST90200634 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24494 levels 6,767 European ancestry individuals NA Affymetrix [15363264] (imputed) 4 X-24494 measurement http://www.ebi.ac.uk/efo/EFO_0800889 GCST90200635 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24544 levels 7,939 European ancestry individuals NA Affymetrix [15417974] (imputed) 3 X-24544 measurement http://www.ebi.ac.uk/efo/EFO_0800892 GCST90200636 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24531 levels 6,455 European ancestry individuals NA Affymetrix [15348017] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200637 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24811 levels 6,349 European ancestry individuals NA Affymetrix [15337675] (imputed) 0 X-24811 measurement http://www.ebi.ac.uk/efo/EFO_0800907 GCST90200638 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24757 levels 6,251 European ancestry individuals NA Affymetrix [15331876] (imputed) 1 X-24757 measurement http://www.ebi.ac.uk/efo/EFO_0800905 GCST90200639 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylxanthine levels 104 South Asian ancestry individuals NA Affymetrix [4454126] (imputed) 0 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90203221 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,7-dimethylurate levels 81 South Asian ancestry individuals NA Affymetrix [4535632] (imputed) 0 3,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800949 GCST90203222 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-gpc (18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4397381] (imputed) 0 1-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800223 GCST90203223 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylxanthine levels 102 South Asian ancestry individuals NA Affymetrix [4488229] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90203224 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-amino-3-methyluracil levels 104 South Asian ancestry individuals NA Affymetrix [4454126] (imputed) 0 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90203225 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,n2-dimethylguanosine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90203226 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N1-methylinosine levels 106 South Asian ancestry individuals NA Affymetrix [4412685] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90203227 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-formylamino-3-methyluracil levels 96 South Asian ancestry individuals NA Affymetrix [4417701] (imputed) 0 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90203228 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotidine levels 103 South Asian ancestry individuals NA Affymetrix [4469647] (imputed) 0 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90203229 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Malonylcarnitine levels 66 South Asian ancestry individuals NA Affymetrix [4408352] (imputed) 0 malonylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800232 GCST90203230 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylcytidine levels 107 South Asian ancestry individuals NA Affymetrix [4394422] (imputed) 0 3-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800633 GCST90203231 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homostachydrine levels 107 South Asian ancestry individuals NA Affymetrix [4392904] (imputed) 0 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90203232 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine degradant levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90203233 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPG (18:0) levels 80 South Asian ancestry individuals NA Affymetrix [4552097] (imputed) 0 1-stearoyl-GPG (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800228 GCST90203234 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylisoleucine levels 107 South Asian ancestry individuals NA Affymetrix [4392767] (imputed) 0 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90203235 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonoyl-gpc (20:4n6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-arachidonoyl-GPC (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800234 GCST90203236 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90203237 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyl-2-pyridone-5-carboxamide levels 105 South Asian ancestry individuals NA Affymetrix [4432773] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90203238 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-2-aminobutyrate levels 101 South Asian ancestry individuals NA Affymetrix [4501781] (imputed) 0 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90203239 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcarnitine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90203240 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoyl-GPC (16:1) levels 107 South Asian ancestry individuals NA Affymetrix [4392821] (imputed) 0 1-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800231 GCST90203241 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPE (18:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800227 GCST90203242 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydodecanedioate levels 83 South Asian ancestry individuals NA Affymetrix [4478576] (imputed) 0 3-hydroxydodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0800226 GCST90203243 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonylglycerol (20:4) levels 99 South Asian ancestry individuals NA Affymetrix [4331535] (imputed) 0 1-arachidonylglycerol (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800224 GCST90203244 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyhippurate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90203245 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyladipate levels 76 South Asian ancestry individuals NA Affymetrix [4374937] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90203271 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyrraline levels 105 South Asian ancestry individuals NA Affymetrix [4433558] (imputed) 0 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90203272 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thymol sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90203273 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylphenol sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90203274 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylphenylsulfate levels 106 South Asian ancestry individuals NA Affymetrix [4410212] (imputed) 0 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90203275 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan betaine levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90203276 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPI (18:1) levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 1-oleoyl-GPI (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800265 GCST90203277 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPI (18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 1-linoleoyl-GPI (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800266 GCST90203278 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPI (16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-GPI (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800257 GCST90203279 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxycaproate levels 76 South Asian ancestry individuals NA Affymetrix [4425253] (imputed) 0 alpha-hydroxycaproate measurement http://www.ebi.ac.uk/efo/EFO_0800261 GCST90203280 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4394422] (imputed) 0 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90203281 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycarnitine levels 107 South Asian ancestry individuals NA Affymetrix [4393796] (imputed) 0 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90203282 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetylglutamine levels 70 South Asian ancestry individuals NA Affymetrix [4573118] (imputed) 0 indoleacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800035 GCST90203283 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-acetyllysine levels 107 South Asian ancestry individuals NA Affymetrix [4391683] (imputed) 0 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90203284 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,4-dihydroxybutyrate levels 105 South Asian ancestry individuals NA Affymetrix [4429977] (imputed) 0 blood 3,4-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022215 GCST90203285 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylglutamine levels 102 South Asian ancestry individuals NA Affymetrix [4499408] (imputed) 0 hexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800262 GCST90203286 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannitol/sorbitol levels 106 South Asian ancestry individuals NA Affymetrix [4415427] (imputed) 0 sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0010533 GCST90203287 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenate (20:3n3 or n6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90203288 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphoethanolamine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90203289 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-cresol sulfate levels 81 South Asian ancestry individuals NA Affymetrix [4519943] (imputed) 0 O-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800955 GCST90203290 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethylarginine (sdma + adma) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90203291 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylalanine levels 103 South Asian ancestry individuals NA Affymetrix [4481688] (imputed) 0 gamma-glutamylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800675 GCST90203292 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylserine levels 107 South Asian ancestry individuals NA Affymetrix [4392767] (imputed) 0 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90203293 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylphenol sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90203294 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800272 GCST90203295 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90203296 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphinganine-1-phosphate levels 105 South Asian ancestry individuals NA Affymetrix [4429216] (imputed) 0 sphinganine-1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800274 GCST90203297 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPE (18:0/18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-stearoyl-2-oleoyl-GPE (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800269 GCST90203298 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels 106 South Asian ancestry individuals NA Affymetrix [4412864] (imputed) 0 glycosyl-N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800275 GCST90203299 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholenate sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4388833] (imputed) 0 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90203300 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxycoumarin levels 78 South Asian ancestry individuals NA Affymetrix [4340691] (imputed) 0 4-hydroxycoumarin measurement http://www.ebi.ac.uk/efo/EFO_0800959 GCST90203301 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,E) levels 107 South Asian ancestry individuals NA Affymetrix [4394255] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203302 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels 98 South Asian ancestry individuals NA Affymetrix [4360109] (imputed) 0 5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800288 GCST90203303 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol sulfate (C21H34O5S) levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 pregnenediol sulfate (C21H34O5S) measurement http://www.ebi.ac.uk/efo/EFO_0800299 GCST90203304 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyglutarate levels 102 South Asian ancestry individuals NA Affymetrix [4478221] (imputed) 0 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90203305 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3alpha, 17alpha) monosulfate (3) levels 105 South Asian ancestry individuals NA Affymetrix [4424148] (imputed) 0 androstenediol (3alpha, 17alpha) monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0800293 GCST90203306 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17alpha-diol disulfate levels 90 South Asian ancestry individuals NA Affymetrix [4542405] (imputed) 0 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90203307 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) monosulfate (2) levels 101 South Asian ancestry individuals NA Affymetrix [4495864] (imputed) 0 androstenediol (3beta,17beta) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800295 GCST90203308 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylproline levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90203309 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotenoid levels (cryptoxanthin) 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 cryptoxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007897 GCST90203310 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20alpha-diol disulfate levels 104 South Asian ancestry individuals NA Affymetrix [4453585] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90203311 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,Z or Z,E) levels 106 South Asian ancestry individuals NA Affymetrix [4404801] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90203312 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinylcarnitine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90203313 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-diol disulfate levels 71 South Asian ancestry individuals NA Affymetrix [4542947] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90203314 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol disulfate (C21H34O8S2) levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 pregnenediol disulfate (C21H34O8S2) measurement http://www.ebi.ac.uk/efo/EFO_0800279 GCST90203315 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Uridine to pseudouridine ratio 8,254 European ancestry individuals NA Affymetrix [15431321] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200774 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine to pyruvate ratio 8,235 European ancestry individuals NA Affymetrix [15430450] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200775 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate to glutamine ratio 8,228 European ancestry individuals NA Affymetrix [15427985] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200776 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Uridine to cytidine ratio 7,705 European ancestry individuals NA Affymetrix [15410596] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200777 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyruvate to 3-methyl-2-oxobutyrate ratio 8,193 European ancestry individuals NA Affymetrix [15428378] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200778 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21470 levels 7,700 European ancestry individuals NA Affymetrix [15411039] (imputed) 6 X-21470 measurement http://www.ebi.ac.uk/efo/EFO_0800817 GCST90200590 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21383 levels 8,226 European ancestry individuals NA Affymetrix [15429866] (imputed) 0 X-21383 measurement http://www.ebi.ac.uk/efo/EFO_0800812 GCST90200591 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21607 levels 7,975 European ancestry individuals NA Affymetrix [15420448] (imputed) 4 X-21607 measurement http://www.ebi.ac.uk/efo/EFO_0800819 GCST90200592 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21834 levels 7,466 European ancestry individuals NA Affymetrix [15398563] (imputed) 1 X-21834 measurement http://www.ebi.ac.uk/efo/EFO_0800833 GCST90200593 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21467 levels 8,195 European ancestry individuals NA Affymetrix [15429611] (imputed) 4 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90200594 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22776 levels 6,944 European ancestry individuals NA Affymetrix [15381079] (imputed) 0 X-22776 measurement http://www.ebi.ac.uk/efo/EFO_0800845 GCST90200595 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23655 levels 6,764 European ancestry individuals NA Affymetrix [15365777] (imputed) 0 X-23655 measurement http://www.ebi.ac.uk/efo/EFO_0800856 GCST90200596 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22834 levels 6,531 European ancestry individuals NA Affymetrix [15353831] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200597 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22771 levels 8,087 European ancestry individuals NA Affymetrix [15425315] (imputed) 0 X-22771 measurement http://www.ebi.ac.uk/efo/EFO_0800844 GCST90200598 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23639 levels 8,272 European ancestry individuals NA Affymetrix [15430149] (imputed) 2 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90200599 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23648 levels 7,357 European ancestry individuals NA Affymetrix [15388281] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200600 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23654 levels 8,241 European ancestry individuals NA Affymetrix [15430653] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200601 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22520 levels 5,389 European ancestry individuals NA Affymetrix [15275085] (imputed) 2 X-22520 measurement http://www.ebi.ac.uk/efo/EFO_0800843 GCST90200602 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23641 levels 6,673 European ancestry individuals NA Affymetrix [15357285] (imputed) 4 X-23641 measurement http://www.ebi.ac.uk/efo/EFO_0800854 GCST90200603 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23276 levels 5,407 European ancestry individuals NA Affymetrix [15280097] (imputed) 0 X-23276 measurement http://www.ebi.ac.uk/efo/EFO_0800847 GCST90200604 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21845 levels 4,874 European ancestry individuals NA Affymetrix [15462393] (imputed) 0 X-21845 measurement http://www.ebi.ac.uk/efo/EFO_0800836 GCST90200605 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22509 levels 5,423 European ancestry individuals NA Affymetrix [15277226] (imputed) 0 X-22509 measurement http://www.ebi.ac.uk/efo/EFO_0800841 GCST90200606 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23644 levels 8,250 European ancestry individuals NA Affymetrix [15431121] (imputed) 1 X-23644 measurement http://www.ebi.ac.uk/efo/EFO_0800855 GCST90200607 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22162 levels 8,249 European ancestry individuals NA Affymetrix [15430997] (imputed) 4 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90200608 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23587 levels 7,662 European ancestry individuals NA Affymetrix [15407271] (imputed) 0 X-23587 measurement http://www.ebi.ac.uk/efo/EFO_0800849 GCST90200609 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23593 levels 7,988 European ancestry individuals NA Affymetrix [15419238] (imputed) 0 X-23593 measurement http://www.ebi.ac.uk/efo/EFO_0800851 GCST90200610 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23636 levels 8,251 European ancestry individuals NA Affymetrix [15430819] (imputed) 0 X-23636 measurement http://www.ebi.ac.uk/efo/EFO_0800852 GCST90200611 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23678 levels 5,745 European ancestry individuals NA Affymetrix [15301846] (imputed) 0 X-23678 measurement http://www.ebi.ac.uk/efo/EFO_0800861 GCST90200612 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23680 levels 8,215 European ancestry individuals NA Affymetrix [15429265] (imputed) 2 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90200613 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23780 levels 7,878 European ancestry individuals NA Affymetrix [15416759] (imputed) 1 X-23780 measurement http://www.ebi.ac.uk/efo/EFO_0800864 GCST90200614 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosatrienoate (22:3n3) levels 89 East Asian ancestry individuals NA Affymetrix [4180715] (imputed) 0 blood 13,16,19-Docosatrienoic acid amount http://purl.obolibrary.org/obo/OBA_2050329 GCST90202148 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tauro-beta-muricholate levels 62 East Asian ancestry individuals NA Affymetrix [4340197] (imputed) 0 tauro-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800213 GCST90202149 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-4-imidazoleacetate levels 98 East Asian ancestry individuals NA Affymetrix [4208861] (imputed) 0 1-methyl-4-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800015 GCST90202150 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-dodecenoate (12:1n7) levels 103 East Asian ancestry individuals NA Affymetrix [4302114] (imputed) 0 5-dodecenoate 12:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021100 GCST90202151 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristoleate (14:1n5) levels 101 East Asian ancestry individuals NA Affymetrix [4334764] (imputed) 0 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90202152 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sebacate (C10-DC) levels 99 East Asian ancestry individuals NA Affymetrix [4198504] (imputed) 0 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90202153 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylasparagine levels 98 East Asian ancestry individuals NA Affymetrix [4211081] (imputed) 0 blood N-acetylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0022206 GCST90202154 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octanoylcarnitine (c8) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90202155 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-undecenoate (11:1n1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90202156 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decanoylcarnitine (C10) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90202157 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPC (16:0) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 1-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800214 GCST90202158 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylarginine levels 103 East Asian ancestry individuals NA Affymetrix [4295850] (imputed) 0 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90202159 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-glutamine levels 103 East Asian ancestry individuals NA Affymetrix [4301505] (imputed) 0 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90202160 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Piperine levels 99 East Asian ancestry individuals NA Affymetrix [4199269] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90202161 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14 levels 102 East Asian ancestry individuals NA Affymetrix [4321259] (imputed) 0 myristoylcarnitine (C14) measurement http://www.ebi.ac.uk/efo/EFO_0800216 GCST90202162 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Campesterol levels 83 East Asian ancestry individuals NA Affymetrix [4313938] (imputed) 0 campesterol measurement http://www.ebi.ac.uk/efo/EFO_0020008 GCST90202163 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearidonate (18:4n3) levels 103 East Asian ancestry individuals NA Affymetrix [4302114] (imputed) 0 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90202164 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylphenylalanine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90202165 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-gpc (18:0) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 1-stearoyl-GPC (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800217 GCST90202166 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPC (18:1) levels 102 East Asian ancestry individuals NA Affymetrix [4316751] (imputed) 0 1-oleoyl-GPC (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800218 GCST90202167 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stachydrine levels 103 East Asian ancestry individuals NA Affymetrix [4301059] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90202168 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Epiandrosterone sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90202169 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylmethionine levels 103 East Asian ancestry individuals NA Affymetrix [4302395] (imputed) 0 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90202170 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylisoleucine levels 91 East Asian ancestry individuals NA Affymetrix [4346546] (imputed) 0 N-acetylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800021 GCST90202171 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-heptadecenoate (17:1n7) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 10-heptadecenoate 17:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021060 GCST90202172 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyglutarate levels 56 African ancestry individuals NA Affymetrix [7641793] (imputed) 0 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90201279 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cinnamoylglycine levels 58 African ancestry individuals NA Affymetrix [7532404] (imputed) 0 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90201280 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylmethionine levels 52 African ancestry individuals NA Affymetrix [7735979] (imputed) 0 S-methylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800042 GCST90201281 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ergothioneine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90201282 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indole-3-carboxylate levels 34 African ancestry individuals NA Affymetrix [7525146] (imputed) 0 indole-3-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800043 GCST90201283 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-(galactosylhydroxy)-L-lysine levels 49 African ancestry individuals NA Affymetrix [7386390] (imputed) 0 5-(galactosylhydroxy)-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800048 GCST90201284 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxyisovalerate levels 59 African ancestry individuals NA Affymetrix [7488508] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90201285 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 13-HODE + 9-HODE levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 13-HODE + 9-HODE measurement http://www.ebi.ac.uk/efo/EFO_0800308 GCST90201286 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (16 or 17)-methylstearate (a19:0 or i19:0) levels 59 African ancestry individuals NA Affymetrix [7496246] (imputed) 0 (16 or 17)-methylstearate (a19:0 or i19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800313 GCST90201287 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2s,3R-dihydroxybutyrate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2s,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800312 GCST90201288 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tridecenedioate (C13:1-DC) levels 56 African ancestry individuals NA Affymetrix [7609845] (imputed) 0 tridecenedioate (C13:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800309 GCST90201289 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoylcarnitine (C10:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 cis-4-decenoylcarnitine (C10:1) measurement http://www.ebi.ac.uk/efo/EFO_0800311 GCST90201290 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutaramate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 alpha-ketoglutaramate measurement http://www.ebi.ac.uk/efo/EFO_0800046 GCST90201291 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutaconate levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 3-methylglutaconate measurement http://www.ebi.ac.uk/efo/EFO_0800047 GCST90201292 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-cholesten-3-one levels 51 African ancestry individuals NA Affymetrix [7719759] (imputed) 0 4-cholesten-3-one measurement http://www.ebi.ac.uk/efo/EFO_0800310 GCST90201293 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2R,3R-dihydroxybutyrate levels 58 African ancestry individuals NA Affymetrix [7518548] (imputed) 0 2R,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800314 GCST90201294 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine disulfide levels 58 African ancestry individuals NA Affymetrix [7514337] (imputed) 0 cysteinylglycine disulfide measurement http://www.ebi.ac.uk/efo/EFO_0800049 GCST90201295 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-3-methylhistidine levels 51 African ancestry individuals NA Affymetrix [7815132] (imputed) 0 N-acetyl-3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800044 GCST90201296 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90201297 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Formiminoglutamate levels 58 African ancestry individuals NA Affymetrix [7521708] (imputed) 0 formiminoglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800050 GCST90201298 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydantoin-5-propionate levels 58 African ancestry individuals NA Affymetrix [7517029] (imputed) 0 hydantoin-5-propionate measurement http://www.ebi.ac.uk/efo/EFO_0800051 GCST90201299 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantoate levels 57 African ancestry individuals NA Affymetrix [7552996] (imputed) 0 blood pantoate measurement http://www.ebi.ac.uk/efo/EFO_0022210 GCST90201300 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-lignoceroyl-GPC (24:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-lignoceroyl-GPC (24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800322 GCST90201301 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-5-imidazoleacetate levels 58 African ancestry individuals NA Affymetrix [7582272] (imputed) 0 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90201302 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90201303 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethyl sulfone levels 56 African ancestry individuals NA Affymetrix [7541987] (imputed) 0 dimethyl sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800979 GCST90201354 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-oxopiperidine-2-carboxylate levels 59 African ancestry individuals NA Affymetrix [7512499] (imputed) 0 6-oxopiperidine-2-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800066 GCST90201355 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-allylcysteine levels 56 African ancestry individuals NA Affymetrix [7571104] (imputed) 0 S-allylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800985 GCST90201356 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-delta-acetylornithine levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90201357 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/14:0, d16:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022105 GCST90201358 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:2/16:0, d18:1/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0022115 GCST90201359 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acisoga levels 57 African ancestry individuals NA Affymetrix [7546300] (imputed) 0 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90201360 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxytyramine sulfate levels 41 African ancestry individuals NA Affymetrix [7833945] (imputed) 0 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90201361 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfone levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90201362 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1H-indole-7-acetic acid levels 40 African ancestry individuals NA Affymetrix [7490666] (imputed) 0 blood 1H-indole-7-acetic acid measurement http://www.ebi.ac.uk/efo/EFO_0022218 GCST90201363 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxymyristate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 blood 3-hydroxymyristate measurement http://www.ebi.ac.uk/efo/EFO_0022197 GCST90202108 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Iminodiacetate (IDA) levels 103 East Asian ancestry individuals NA Affymetrix [4303061] (imputed) 0 iminodiacetate (IDA) measurement http://www.ebi.ac.uk/efo/EFO_0800945 GCST90202109 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoylglycerol (18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800195 GCST90202110 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxobutyrate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90202111 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-linoleoylglycerol (18:2) levels 86 East Asian ancestry individuals NA Affymetrix [4240559] (imputed) 0 2-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800197 GCST90202112 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homocitrulline levels 101 East Asian ancestry individuals NA Affymetrix [4339133] (imputed) 0 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90202113 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800198 GCST90202114 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homoarginine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST90202115 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citramalate levels 84 East Asian ancestry individuals NA Affymetrix [4285146] (imputed) 0 blood citramalate measurement http://www.ebi.ac.uk/efo/EFO_0022198 GCST90202116 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Galactonate levels 89 East Asian ancestry individuals NA Affymetrix [4190149] (imputed) 0 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90202117 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate levels 73 East Asian ancestry individuals NA Affymetrix [4304841] (imputed) 0 glycolithocholate measurement http://www.ebi.ac.uk/efo/EFO_0800203 GCST90202118 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trigonelline levels 103 East Asian ancestry individuals NA Affymetrix [4302841] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90202119 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltyrosine levels 99 East Asian ancestry individuals NA Affymetrix [4201137] (imputed) 0 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90202120 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylhistidine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90202121 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. EDTA levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 EDTA measurement http://www.ebi.ac.uk/efo/EFO_0800946 GCST90202122 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolebutyrate levels 68 East Asian ancestry individuals NA Affymetrix [4175050] (imputed) 0 3-Indolebutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021559 GCST90202198 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylxanthine levels 98 East Asian ancestry individuals NA Affymetrix [4220029] (imputed) 0 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90202199 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,n2-dimethylguanosine levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90202200 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90202201 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotidine levels 100 East Asian ancestry individuals NA Affymetrix [4351483] (imputed) 0 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90202202 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N1-methylinosine levels 101 East Asian ancestry individuals NA Affymetrix [4334802] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90202203 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-formylamino-3-methyluracil levels 90 East Asian ancestry individuals NA Affymetrix [4355960] (imputed) 0 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90202204 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-carbamoylthreonyladenosine levels 102 East Asian ancestry individuals NA Affymetrix [4317062] (imputed) 0 N6-carbamoylthreonyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800629 GCST90202205 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,7-dimethyluric acid levels 97 East Asian ancestry individuals NA Affymetrix [4236371] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90202206 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine-glutathione disulfide levels 97 East Asian ancestry individuals NA Affymetrix [4223918] (imputed) 0 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90202207 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerylglycine levels 87 East Asian ancestry individuals NA Affymetrix [4229863] (imputed) 0 isovalerylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800025 GCST90202208 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPG (18:0) levels 92 East Asian ancestry individuals NA Affymetrix [4329229] (imputed) 0 1-stearoyl-GPG (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800228 GCST90202209 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methyluridine (ribothymidine) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90202210 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPE (18:0) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 1-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800227 GCST90202211 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydodecanedioate levels 89 East Asian ancestry individuals NA Affymetrix [4195624] (imputed) 0 3-hydroxydodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0800226 GCST90202212 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylcytidine levels 101 East Asian ancestry individuals NA Affymetrix [4333612] (imputed) 0 3-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800633 GCST90202213 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylguanine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90202214 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyl-2-pyridone-5-carboxamide levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90202215 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Malonylcarnitine levels 67 East Asian ancestry individuals NA Affymetrix [4185467] (imputed) 0 malonylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800232 GCST90202216 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylglycine levels 80 East Asian ancestry individuals NA Affymetrix [4375214] (imputed) 0 hexanoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800233 GCST90202217 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine degradant levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90202218 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoyl-GPC (16:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800231 GCST90202219 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90202220 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylisoleucine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90202221 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcarnitine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90202222 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-nonadecenoate (19:1n9) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 10-nonadecenoate 19:1n9 measurement http://www.ebi.ac.uk/efo/EFO_0021061 GCST90202173 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglycine levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90202174 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoate (20:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 eicosenoate (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800220 GCST90202175 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltryptophan levels 101 East Asian ancestry individuals NA Affymetrix [4328482] (imputed) 0 gamma-glutamyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800671 GCST90202176 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxyisovalerate levels 103 East Asian ancestry individuals NA Affymetrix [4300166] (imputed) 0 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90202177 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylthreonine levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90202178 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylproline levels 88 East Asian ancestry individuals NA Affymetrix [4196492] (imputed) 0 blood N-acetylproline measurement http://www.ebi.ac.uk/efo/EFO_0022207 GCST90202179 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylhistidine levels 87 East Asian ancestry individuals NA Affymetrix [4226846] (imputed) 0 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90202180 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hyocholate levels 83 East Asian ancestry individuals NA Affymetrix [4304044] (imputed) 0 hyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800219 GCST90202181 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylthreonine levels 102 East Asian ancestry individuals NA Affymetrix [4314345] (imputed) 0 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90202182 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenate [alpha or gamma; (18:3n3 or 6)] levels 103 East Asian ancestry individuals NA Affymetrix [4301369] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90202183 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcarnitine levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90202184 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90202185 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aconitate [cis or trans] levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90202186 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythronate levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90202187 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Laurylcarnitine levels 103 East Asian ancestry individuals NA Affymetrix [4302395] (imputed) 0 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90202188 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyhippurate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90202189 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-amino-3-carboxypropyl)uridine levels 93 East Asian ancestry individuals NA Affymetrix [4305477] (imputed) 0 3-(3-amino-3-carboxypropyl)uridine measurement http://www.ebi.ac.uk/efo/EFO_0800632 GCST90202190 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3,7-trimethylurate levels 87 East Asian ancestry individuals NA Affymetrix [4229803] (imputed) 0 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90202191 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5,6-dihydrouridine levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 5,6-dihydrouridine measurement http://www.ebi.ac.uk/efo/EFO_0800631 GCST90202192 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylxanthine levels 94 East Asian ancestry individuals NA Affymetrix [4287708] (imputed) 0 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90202193 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerylcarnitine (C5) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 isovalerylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800024 GCST90202194 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-gpc (18:2) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 1-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800223 GCST90202195 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-amino-3-methyluracil levels 95 East Asian ancestry individuals NA Affymetrix [4275189] (imputed) 0 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90202196 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,7-dimethylurate levels 76 East Asian ancestry individuals NA Affymetrix [4249905] (imputed) 0 3,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800949 GCST90202197 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole propionate levels 51 African ancestry individuals NA Affymetrix [7746677] (imputed) 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90201329 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinimide levels 44 African ancestry individuals NA Affymetrix [7680862] (imputed) 0 blood succinimide measurement http://www.ebi.ac.uk/efo/EFO_0022211 GCST90201330 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-stearoyl-GPE (18:0) levels 58 African ancestry individuals NA Affymetrix [7538056] (imputed) 0 2-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800343 GCST90201331 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (R)-3-hydroxybutyrylcarnitine levels 48 African ancestry individuals NA Affymetrix [7448540] (imputed) 0 (R)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800344 GCST90201332 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trimethylamine n-oxide levels 59 African ancestry individuals NA Affymetrix [7494771] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90201333 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcarnosine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 blood N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022217 GCST90201334 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyltaurine levels 47 African ancestry individuals NA Affymetrix [7426864] (imputed) 0 N-methyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800064 GCST90201335 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margaroylcarnitine (C17) levels 57 African ancestry individuals NA Affymetrix [7533347] (imputed) 0 margaroylcarnitine (C17) measurement http://www.ebi.ac.uk/efo/EFO_0800345 GCST90201336 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnanediol-3-glucuronide levels 58 African ancestry individuals NA Affymetrix [7514512] (imputed) 0 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90201337 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lanthionine levels 55 African ancestry individuals NA Affymetrix [7582623] (imputed) 0 lanthionine measurement http://www.ebi.ac.uk/efo/EFO_0800063 GCST90201338 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxydecanoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800347 GCST90201339 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine betaine (hercynine) levels 57 African ancestry individuals NA Affymetrix [7616183] (imputed) 0 histidine betaine (hercynine) measurement http://www.ebi.ac.uk/efo/EFO_0800972 GCST90201340 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycohyocholate levels 55 African ancestry individuals NA Affymetrix [7661242] (imputed) 0 glycohyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800346 GCST90201341 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3b-hydroxy-5-cholenoic acid levels 50 African ancestry individuals NA Affymetrix [7393044] (imputed) 0 3b-hydroxy-5-cholenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800348 GCST90201342 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (1) levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90201343 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (2) levels 32 African ancestry individuals NA Affymetrix [7491723] (imputed) 0 3-methyl catechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800973 GCST90201344 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolin-2-one levels 49 African ancestry individuals NA Affymetrix [7413446] (imputed) 0 indolin-2-one measurement http://www.ebi.ac.uk/efo/EFO_0800981 GCST90201345 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylcatechol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90201346 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-acetylphenol sulfate levels 47 African ancestry individuals NA Affymetrix [7500632] (imputed) 0 3-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800983 GCST90201347 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminophenol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90201348 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminooctanoate levels 58 African ancestry individuals NA Affymetrix [7540730] (imputed) 0 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90201349 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC glucuronide levels 48 African ancestry individuals NA Affymetrix [7576467] (imputed) 0 gamma-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800165 GCST90201350 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-1-methylhistidine levels 56 African ancestry individuals NA Affymetrix [7696068] (imputed) 0 N-acetyl-1-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800065 GCST90201351 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-piperidinone levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-piperidinone measurement http://www.ebi.ac.uk/efo/EFO_0800980 GCST90201352 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guaiacol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 guaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800978 GCST90201353 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonate levels 103 East Asian ancestry individuals NA Affymetrix [4302331] (imputed) 0 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90202123 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyridoxate levels 103 East Asian ancestry individuals NA Affymetrix [4300441] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90202124 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoylglycerol (18:2) levels 103 East Asian ancestry individuals NA Affymetrix [4303061] (imputed) 0 1-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800199 GCST90202125 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3-dimethylurate levels 83 East Asian ancestry individuals NA Affymetrix [4306800] (imputed) 0 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90202126 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90202127 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylcarnitine (c4) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90202128 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolepropionate levels 99 East Asian ancestry individuals NA Affymetrix [4192281] (imputed) 0 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90202129 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecanedioate levels 102 East Asian ancestry individuals NA Affymetrix [4314243] (imputed) 0 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90202130 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetate levels 103 East Asian ancestry individuals NA Affymetrix [4300748] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90202131 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylvaline levels 103 East Asian ancestry individuals NA Affymetrix [4298015] (imputed) 0 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90202132 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglycine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90202133 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C4 levels 101 East Asian ancestry individuals NA Affymetrix [4338977] (imputed) 0 butyrylcarnitine (C4) measurement http://www.ebi.ac.uk/efo/EFO_0800201 GCST90202134 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxylaurate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-hydroxylaurate measurement http://www.ebi.ac.uk/efo/EFO_0800204 GCST90202135 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylxanthine levels 100 East Asian ancestry individuals NA Affymetrix [4356056] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90202136 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxysebacate levels 89 East Asian ancestry individuals NA Affymetrix [4201752] (imputed) 0 3-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800205 GCST90202137 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrylglycine levels 69 East Asian ancestry individuals NA Affymetrix [4143588] (imputed) 0 butyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800208 GCST90202138 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyhexanoate levels 79 East Asian ancestry individuals NA Affymetrix [4174197] (imputed) 0 5-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800206 GCST90202139 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylcarnitine (c3) levels 103 East Asian ancestry individuals NA Affymetrix [4301041] (imputed) 0 propionylcarnitine (C3) measurement http://www.ebi.ac.uk/efo/EFO_0800210 GCST90202140 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylglycine levels 89 East Asian ancestry individuals NA Affymetrix [4173851] (imputed) 0 propionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800207 GCST90202141 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-ethylpropionate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90202142 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90202143 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate n3 DPA; 22:5n3 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 docosapentaenoate n3 DPA; 22:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021048 GCST90202144 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adrenate (22:4n6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90202145 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosadienoate (22:2n6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 docosadienoate (22:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800211 GCST90202146 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pro-hydroxy-pro levels 102 East Asian ancestry individuals NA Affymetrix [4318311] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90202147 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPC (p-16:0) levels 58 African ancestry individuals NA Affymetrix [7517340] (imputed) 0 1-(1-enyl-palmitoyl)-GPC (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800323 GCST90201304 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPE (p-16:0) levels 59 African ancestry individuals NA Affymetrix [7492232] (imputed) 0 1-(1-enyl-palmitoyl)-GPE (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800334 GCST90201305 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C18:2 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90201306 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosadioate (C22-DC) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 docosadioate (C22-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800331 GCST90201307 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-GPE (p-18:0) levels 59 African ancestry individuals NA Affymetrix [7492232] (imputed) 0 1-(1-enyl-stearoyl)-GPE (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800335 GCST90201308 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosanedioate (C20-DC) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 eicosanedioate (C20-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800330 GCST90201309 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine sulfoxide levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 S-methylcysteine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0800058 GCST90201310 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-oxo-retinoic acid levels 52 African ancestry individuals NA Affymetrix [7721198] (imputed) 0 blood 4-oxo-retinoic acid measurement http://www.ebi.ac.uk/efo/EFO_0022216 GCST90201311 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxy-2-oxoglutaric acid levels 55 African ancestry individuals NA Affymetrix [7599978] (imputed) 0 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90201312 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-oleoyltaurine levels 51 African ancestry individuals NA Affymetrix [7816574] (imputed) 0 N-oleoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800337 GCST90201313 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone glucuronide levels 59 African ancestry individuals NA Affymetrix [7500737] (imputed) 0 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90201314 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 S-methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800054 GCST90201315 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Argininate levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 argininate measurement http://www.ebi.ac.uk/efo/EFO_0800055 GCST90201316 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoate (10:1n6) levels 59 African ancestry individuals NA Affymetrix [7496805] (imputed) 0 cis-4-decenoate (10:1n6) measurement http://www.ebi.ac.uk/efo/EFO_0800318 GCST90201317 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-oxoarginine levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90201318 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyglutamate levels 53 African ancestry individuals NA Affymetrix [7697999] (imputed) 0 4-hydroxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800052 GCST90201319 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carboxyethyl-gaba levels 57 African ancestry individuals NA Affymetrix [7536957] (imputed) 0 carboxyethyl-GABA measurement http://www.ebi.ac.uk/efo/EFO_0800059 GCST90201320 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-o-methylascorbic acid levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-O-methylascorbic acid measurement http://www.ebi.ac.uk/efo/EFO_0800164 GCST90201321 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-methyllysine levels 58 African ancestry individuals NA Affymetrix [7523319] (imputed) 0 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90201322 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulate levels 44 African ancestry individuals NA Affymetrix [7762630] (imputed) 0 dihydroferulate measurement http://www.ebi.ac.uk/efo/EFO_0800969 GCST90201323 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alliin levels 50 African ancestry individuals NA Affymetrix [7308983] (imputed) 0 alliin measurement http://www.ebi.ac.uk/efo/EFO_0800970 GCST90201324 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoylglycine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-palmitoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800342 GCST90201325 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-citrylglutamate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90201326 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannonate levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 mannonate measurement http://www.ebi.ac.uk/efo/EFO_0800971 GCST90201327 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Prolylglycine levels 58 African ancestry individuals NA Affymetrix [7555435] (imputed) 0 prolylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800683 GCST90201328 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-2-aminobutyrate levels 102 East Asian ancestry individuals NA Affymetrix [4313953] (imputed) 0 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90202223 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonylglycerol (20:4) levels 98 East Asian ancestry individuals NA Affymetrix [4209760] (imputed) 0 1-arachidonylglycerol (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800224 GCST90202224 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcitrulline levels 79 East Asian ancestry individuals NA Affymetrix [4171327] (imputed) 0 N-acetylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800028 GCST90202225 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90203787 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(4-hydroxyphenyl)lactate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90203788 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyphenylacetate levels 102 South Asian ancestry individuals NA Affymetrix [4486738] (imputed) 0 2-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800131 GCST90203789 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90203790 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate levels 106 South Asian ancestry individuals NA Affymetrix [4409972] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90203791 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisone levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90203792 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarate (C5-DC) levels 99 South Asian ancestry individuals NA Affymetrix [4337645] (imputed) 0 glutarate (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800620 GCST90203793 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90203794 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphinganine levels 92 South Asian ancestry individuals NA Affymetrix [4481902] (imputed) 0 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90203795 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Biliverdin levels 107 South Asian ancestry individuals NA Affymetrix [4394255] (imputed) 0 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90203796 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphocholine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90203797 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90203798 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guanidinoacetate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90203799 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine levels 107 South Asian ancestry individuals NA Affymetrix [4388259] (imputed) 0 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90203800 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholate levels 84 South Asian ancestry individuals NA Affymetrix [4456083] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90203801 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90203802 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-alanine levels 106 South Asian ancestry individuals NA Affymetrix [4415489] (imputed) 0 beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0800640 GCST90203803 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystathionine levels 104 South Asian ancestry individuals NA Affymetrix [4457334] (imputed) 0 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90203804 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-Hydroxybutyrate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90203805 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90203806 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gluconate levels 103 South Asian ancestry individuals NA Affymetrix [4462044] (imputed) 0 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90203807 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine levels 106 South Asian ancestry individuals NA Affymetrix [4415808] (imputed) 0 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90203808 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3195) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280012 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_32) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280013 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_320) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280014 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3205) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280015 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3208) (Fenson) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 200 fenson measurement http://www.ebi.ac.uk/efo/EFO_0803497 GCST90280016 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3224) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280017 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3228) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280018 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3238) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280019 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3248) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280020 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3252) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280021 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3258) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280022 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3259) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280023 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3262) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280024 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3263) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280025 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3269) (5-(Hydroxyphenyl)-gamma-valerolactone-O-sulphate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 5-(hydroxyphenyl)-gamma-valerolactone-O-sulphate measurement http://www.ebi.ac.uk/efo/EFO_0803393 GCST90280026 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3281) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280027 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3288) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280028 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3299) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280029 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3309) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280030 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3310) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280031 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_332) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280032 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3320) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280033 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3325) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280034 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3337) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280035 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3345) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280036 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4599) (Glycerol triundecanoate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 glycerol triundecanoate measurement http://www.ebi.ac.uk/efo/EFO_0803419 GCST90279356 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4604) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279357 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4304) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279305 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4608) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279358 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4609) (Delphinine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 delphinine measurement http://www.ebi.ac.uk/efo/EFO_0803493 GCST90279359 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4612) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279360 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4613) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279361 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4615) (Phorbol 12-tiglate 13-decanoate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 phorbol 12-tiglate 13-decanoate measurement http://www.ebi.ac.uk/efo/EFO_0803508 GCST90279362 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3490) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280062 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3494) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280063 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3500) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280064 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3505) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280065 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3507) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280066 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3528) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280067 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3534) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280068 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3555) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280069 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3556) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280070 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3559) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280071 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3562) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280072 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3564) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280073 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3579) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280074 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3588) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280075 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3589) (sphinga-4E8E10E-trienine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 level of (4E,8E,10E-d18:3)sphingosine in blood serum http://purl.obolibrary.org/obo/OBA_2045044 GCST90280076 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3598) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280077 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_36) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280078 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2993) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279976 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2997) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279977 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_300) (()-2-Methylthiazolidine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 ()-2-methylthiazolidine measurement http://www.ebi.ac.uk/efo/EFO_0803383 GCST90279978 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3001) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279979 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3002) (9Z-hexadecenamide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of palmitoleamide in blood serum http://purl.obolibrary.org/obo/OBA_2045040 GCST90279980 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3013) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279981 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_302) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279982 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3022) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279983 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3028) (Diethylenetriamine crosslinked with epichlorohydrin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 diethylenetriamine crosslinked with epichlorohydrin measurement http://www.ebi.ac.uk/efo/EFO_0803414 GCST90279984 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3034) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279985 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3040) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279986 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3046) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279987 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3055) (Barban) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279988 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3057) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279989 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3071) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279990 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3081) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279991 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3084) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279992 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3093) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279993 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3095) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279994 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3099) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279995 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3102) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279996 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3106) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279997 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3108) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279998 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3113) (Pisatoside) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279999 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3117) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280000 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2832) (Zinc lactate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 zinc lactate measurement http://www.ebi.ac.uk/efo/EFO_0803522 GCST90279951 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2842) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279952 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2868) (Polyethylene oxidized) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 polyethylene oxidized measurement http://www.ebi.ac.uk/efo/EFO_0803450 GCST90279953 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2871) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279954 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2872) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279955 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2878) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279956 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2882) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279957 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2888) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279958 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2893) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279959 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2894) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279960 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2908) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 52 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279961 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_291) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279962 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2910) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279963 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2916) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279964 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2921) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279965 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2934) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279966 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2941) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279967 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2952) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279968 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_296) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279969 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2960) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279970 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2961) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279971 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2971) (7-Methylpyrido34-cpsoralen) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 7-methylpyrido34-cpsoralen measurement http://www.ebi.ac.uk/efo/EFO_0803479 GCST90279972 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2974) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279973 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2985) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279974 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2986) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279975 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_403) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279257 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4034) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279258 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4040) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279259 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4041) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279260 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4054) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279261 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4065) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279262 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4075) (1-(9Z-octadecenoyl)-sn-glycero-3-phosphoserine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of 1-O-oleoyl-sn-glycero-3-phosphoserine in blood serum http://purl.obolibrary.org/obo/OBA_2045055 GCST90279263 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4077) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279264 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_408) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279265 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4086) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279266 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4094) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279267 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4096) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279268 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_410) (L-Malic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 L-Malic acid measurement http://www.ebi.ac.uk/efo/EFO_0021622 GCST90279269 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4109) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279270 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4119) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279271 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4120) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279272 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4122) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279273 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4128) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279274 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4139) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279275 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_414) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279276 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4142) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279277 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4146) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279278 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4154) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279279 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_416) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279280 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4169) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279281 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3362) (Glycerophosphocholine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 glycerophosphocholine measurement http://www.ebi.ac.uk/efo/EFO_0010489 GCST90280037 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3367) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280038 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3380) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280039 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3381) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280040 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3386) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280041 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3392) (4-Hydroxyphenylacetylglutamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90280042 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3393) (Alverine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 alverine measurement http://www.ebi.ac.uk/efo/EFO_0803401 GCST90280043 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3410) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280044 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3411) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280045 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3412) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280046 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3418) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280047 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_342) (3-Methylthiopropanamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280048 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3429) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280049 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_343) (3-Methylthiopropanamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280050 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3436) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280051 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3438) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280052 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_344) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280053 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3440) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280054 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3444) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280055 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_348) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280060 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3485) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280061 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4291) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279302 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4295) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279303 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_430) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279304 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4271) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279301 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3119) (Panaxydol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280001 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3125) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280002 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3126) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280003 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3133) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280004 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3138) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280005 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3139) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280006 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3144) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280007 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3150) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280008 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3155) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280009 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3938) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279241 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3943) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279242 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3944) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279243 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3953) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279244 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3973) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279245 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3994) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279246 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3999) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279247 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4001) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279248 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4002) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279249 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4005) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279250 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4007) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279251 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4012) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279252 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4015) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279253 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4020) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279254 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4025) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279255 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4026) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279256 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4308) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279306 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_431) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279307 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4310) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279308 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4311) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279309 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4315) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 16 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279310 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4319) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279311 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4327) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279312 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4333) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279313 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4335) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279314 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4339) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279315 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4347) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279316 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4358) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279317 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4363) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279318 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4369) (4-Glutathionyl cyclophosphamide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279319 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4373) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279320 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4377) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279321 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_438) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279322 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4392) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279323 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4405) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279324 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4409) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279325 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_442) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279326 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4427) (1-hexadecanoyl-sn-glycero-3-phospho-(1-myo-inositol)) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279327 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4437) (DG(15:018:4(6Z9Z12Z15Z)0:0)) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279328 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_444) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279329 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4455) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279330 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_417) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279282 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4178) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279283 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4179) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279284 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_418) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279285 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4181) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279286 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4185) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279287 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4209) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279288 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4217) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279289 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4230) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279290 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4232) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279291 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4237) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279292 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4238) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279293 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_424) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279294 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4241) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279295 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4243) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279296 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4251) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279297 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4254) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279298 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4262) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279299 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4265) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279300 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3452) (Myristoylglycine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 myristoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0803434 GCST90280056 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3467) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280057 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3468) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280058 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3473) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280059 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_318) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280010 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3182) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280011 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7478) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280787 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_748) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280788 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7484) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280789 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7486) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280790 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7488) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280791 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7493) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280792 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7504) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280793 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_751) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280794 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7538) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280795 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7542) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280796 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7555) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280797 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7560) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280798 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7562) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280799 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7566) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280800 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7571) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280801 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7574) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280802 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7576) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280803 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7578) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280804 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7579) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 71 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280805 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_758) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280806 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7582) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280807 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7586) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 73 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280808 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7597) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280809 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_760) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280810 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7605) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280811 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7049) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280712 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7064) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280713 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7068) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280714 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7073) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280715 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7076) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 19 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280716 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7105) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280717 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7124) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280718 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7140) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280719 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7145) (p-Coumaroyl vitisin A) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 p-coumaroyl vitisin A measurement http://www.ebi.ac.uk/efo/EFO_0803444 GCST90280720 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7147) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280721 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7154) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280722 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7163) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280723 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7166) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280724 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7167) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280725 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7175) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 20 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280726 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7177) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280727 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7184) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280728 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7185) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 13 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280729 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7186) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280730 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7190) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280731 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7191) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 57 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280732 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7201) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280733 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7205) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280734 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7206) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280735 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7209) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280736 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7210) (N-(2-hydroxy-docosanoyl)-pentadecasphing-4-enine-1-phosphoethanolamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of ceramide phosphoethanolamine in blood serum http://purl.obolibrary.org/obo/OBA_2045057 GCST90280737 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7211) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280738 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7214) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280739 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7218) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280740 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7220) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280741 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7223) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280742 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7228) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280743 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7230) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280744 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7231) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280745 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7232) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280746 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7234) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280747 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7237) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280748 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7243) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280749 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7250) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280750 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7252) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280751 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7259) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280752 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_726) (Dichloroacetate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280753 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7267) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280754 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7269) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280755 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_727) (5-Hydroxy-2-furoic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 5-hydroxy-2-furoic acid measurement http://www.ebi.ac.uk/efo/EFO_0803394 GCST90280756 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7270) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280757 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7277) (Licoagrodin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 licoagrodin measurement http://www.ebi.ac.uk/efo/EFO_0803427 GCST90280758 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7279) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280759 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7286) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280760 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7304) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280761 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6929) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280687 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6933) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280688 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6936) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280689 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6944) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280690 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6950) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280691 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6959) (Cucurbitacin I 2-glucoside) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 cucurbitacin I 2-glucoside measurement http://www.ebi.ac.uk/efo/EFO_0803409 GCST90280692 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6961) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280693 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6962) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280694 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6968) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280695 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6978) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280696 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6985) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280697 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6995) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280698 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_6998) (Glycogen) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280699 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7004) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280700 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7009) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280701 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7011) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280702 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7013) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280703 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7025) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280704 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7026) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280705 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_703) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280706 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7034) (Tetrasaccharide (Glycogen, Stachyose)) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 tetrasaccharide (glycogen, stachyose) measurement http://www.ebi.ac.uk/efo/EFO_0803459 GCST90280707 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7038) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280708 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7043) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280709 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7046) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280710 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7048) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280711 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7616) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280812 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7618) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280813 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7620) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280814 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7622) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280815 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7630) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280816 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7632) (Correolide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 correolide measurement http://www.ebi.ac.uk/efo/EFO_0803490 GCST90280817 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7633) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280818 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7640) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280819 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_765) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280820 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7651) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280821 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7652) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280822 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7653) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280823 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7658) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280824 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_766) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280825 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7663) (A 77003) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 A 77003 measurement http://www.ebi.ac.uk/efo/EFO_0803480 GCST90280826 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7680) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280827 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_769) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280828 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7698) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280829 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7700) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280830 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7706) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280831 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7711) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 21 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280832 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7716) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280833 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7718) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280834 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7735) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280835 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7737) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280836 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7937) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280862 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7938) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280863 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7941) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280864 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7942) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280865 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7947) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280866 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7960) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280867 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7977) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280868 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7985) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280869 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8013) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280870 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_802) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280871 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8024) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280872 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8027) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280873 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8043) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280874 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8046) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280875 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8056) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280876 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8068) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280877 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8071) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280878 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8072) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280879 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8077) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280880 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8084) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280881 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8089) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280882 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8090) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280883 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8096) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280884 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_81) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280885 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8107) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280886 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7741) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280837 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7743) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280838 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7772) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280839 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7779) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280840 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7782) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280841 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7785) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280842 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7786) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280843 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7787) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280844 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7790) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280845 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7791) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280846 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7797) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280847 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7803) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280848 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7808) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280849 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7833) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280850 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7835) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280851 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7842) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280852 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7843) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280853 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7854) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280854 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7861) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280855 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_788) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280856 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7880) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280857 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7898) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280858 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7902) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280859 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7929) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280860 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7934) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280861 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8110) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280887 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8128) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280888 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8134) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280889 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8135) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280890 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8142) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280891 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8150) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280892 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8153) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280893 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8159) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280894 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8160) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280895 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8167) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280896 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_817) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280897 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8170) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280898 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8172) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280899 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8180) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280900 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8188) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280901 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8197) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280902 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8199) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280903 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8205) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280904 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8208) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280905 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8213) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280906 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8221) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280907 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8223) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280908 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8227) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280909 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8230) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280910 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_8232) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280911 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7305) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280762 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7309) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280763 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7315) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280764 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7337) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280765 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7339) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280766 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_735) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280767 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7350) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280768 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_737) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280769 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7373) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280770 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7375) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280771 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7378) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280772 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7379) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280773 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_742) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280774 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7421) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280775 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_743) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280776 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7430) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280777 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7431) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280778 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7435) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280779 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7436) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280780 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7437) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280781 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7439) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280782 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7463) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280783 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7469) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280784 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7474) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280785 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_7475) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280786 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25957 levels 7,335 European ancestry individuals NA Affymetrix [15393810] (imputed) 0 X-25957 measurement http://www.ebi.ac.uk/efo/EFO_0800938 GCST90200660 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25422 levels 8,210 European ancestry individuals NA Affymetrix [15430495] (imputed) 4 X-25422 measurement http://www.ebi.ac.uk/efo/EFO_0800927 GCST90200661 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25790 levels 8,221 European ancestry individuals NA Affymetrix [15429764] (imputed) 1 X-25790 measurement http://www.ebi.ac.uk/efo/EFO_0800933 GCST90200662 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25420 levels 8,271 European ancestry individuals NA Affymetrix [15431271] (imputed) 2 X-25420 measurement http://www.ebi.ac.uk/efo/EFO_0800926 GCST90200663 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25810 levels 8,167 European ancestry individuals NA Affymetrix [15427088] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200664 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25433 levels 6,516 European ancestry individuals NA Affymetrix [15353611] (imputed) 3 X-25433 measurement http://www.ebi.ac.uk/efo/EFO_0800928 GCST90200665 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25343 levels 8,195 European ancestry individuals NA Affymetrix [15427837] (imputed) 0 X-25343 measurement http://www.ebi.ac.uk/efo/EFO_0800922 GCST90200666 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25271 levels 7,906 European ancestry individuals NA Affymetrix [15419139] (imputed) 0 X-25271 measurement http://www.ebi.ac.uk/efo/EFO_0800920 GCST90200667 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25520 levels 7,997 European ancestry individuals NA Affymetrix [15422133] (imputed) 0 X-25520 measurement http://www.ebi.ac.uk/efo/EFO_0800931 GCST90200668 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25519 levels 8,080 European ancestry individuals NA Affymetrix [15425390] (imputed) 0 X-25519 measurement http://www.ebi.ac.uk/efo/EFO_0800930 GCST90200669 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26111 levels 8,002 European ancestry individuals NA Affymetrix [15423826] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200670 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26109 levels 6,992 European ancestry individuals NA Affymetrix [15377098] (imputed) 6 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200671 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26054 levels 8,046 European ancestry individuals NA Affymetrix [15423547] (imputed) 4 X-26054 measurement http://www.ebi.ac.uk/efo/EFO_0800939 GCST90200672 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C4 levels 8,111 European ancestry individuals NA Affymetrix [15426976] (imputed) 6 butyrylcarnitine (C4) measurement http://www.ebi.ac.uk/efo/EFO_0800201 GCST90200673 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone sulfate levels 8,182 European ancestry individuals NA Affymetrix [15428238] (imputed) 7 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90200674 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltyrosine levels 7,841 European ancestry individuals NA Affymetrix [15413664] (imputed) 2 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90200675 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-glutamine levels 8,181 European ancestry individuals NA Affymetrix [15428829] (imputed) 2 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90200676 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylphenylalanine levels 8,228 European ancestry individuals NA Affymetrix [15430074] (imputed) 4 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90200677 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylasparagine levels 7,935 European ancestry individuals NA Affymetrix [15419345] (imputed) 2 blood N-acetylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0022206 GCST90200678 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylarginine levels 8,271 European ancestry individuals NA Affymetrix [15431504] (imputed) 4 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90200679 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-formylamino-3-methyluracil levels 7,599 European ancestry individuals NA Affymetrix [15405151] (imputed) 2 5-acetylamino-6-formylamino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800950 GCST90200680 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotidine levels 8,017 European ancestry individuals NA Affymetrix [15423203] (imputed) 1 orotidine measurement http://www.ebi.ac.uk/efo/EFO_0800630 GCST90200681 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylcytidine levels 8,117 European ancestry individuals NA Affymetrix [15424688] (imputed) 3 3-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800633 GCST90200682 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcitrulline levels 7,324 European ancestry individuals NA Affymetrix [15393120] (imputed) 1 N-acetylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800028 GCST90200683 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-aspartyl-glutamate (naag) levels 7,705 European ancestry individuals NA Affymetrix [15413041] (imputed) 8 N-acetyl-aspartyl-glutamate (NAAG) measurement http://www.ebi.ac.uk/efo/EFO_0800033 GCST90200684 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,Z or Z,E) levels 8,238 European ancestry individuals NA Affymetrix [15430245] (imputed) 2 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200687 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone glucuronide levels 7,980 European ancestry individuals NA Affymetrix [15419895] (imputed) 4 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90200688 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-methyllysine levels 8,299 European ancestry individuals NA Affymetrix [15432359] (imputed) 3 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90200689 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-1-methylhistidine levels 7,588 European ancestry individuals NA Affymetrix [15406311] (imputed) 2 N-acetyl-1-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800065 GCST90200690 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-delta-acetylornithine levels 8,259 European ancestry individuals NA Affymetrix [15430697] (imputed) 1 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90200691 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 8,238 European ancestry individuals NA Affymetrix [15429442] (imputed) 3 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800390 GCST90200692 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate glucuronide (1) levels 8,236 European ancestry individuals NA Affymetrix [15430142] (imputed) 4 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90200693 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methylcytidine levels 8,122 European ancestry individuals NA Affymetrix [15425870] (imputed) 2 2'-O-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800635 GCST90200694 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methyluridine levels 7,582 European ancestry individuals NA Affymetrix [15405356] (imputed) 1 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90200695 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,N6-dimethyllysine levels 8,265 European ancestry individuals NA Affymetrix [15430926] (imputed) 1 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90200696 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6,N6-dimethyllysine levels 7,891 European ancestry individuals NA Affymetrix [15417571] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200697 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6-methyllysine levels 8,069 European ancestry individuals NA Affymetrix [15425198] (imputed) 3 N2-acetyl,N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800109 GCST90200698 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid glucuronide levels 8,060 European ancestry individuals NA Affymetrix [15424888] (imputed) 4 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90200699 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decadienedioic acid (C10:2-DC) levels 8,131 European ancestry individuals NA Affymetrix [15425095] (imputed) 7 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90200700 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (1) levels 8,254 European ancestry individuals NA Affymetrix [15429429] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200701 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (2) levels 8,255 European ancestry individuals NA Affymetrix [15429677] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200702 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (3) levels 8,253 European ancestry individuals NA Affymetrix [15429420] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200703 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (z,z) levels 8,261 European ancestry individuals NA Affymetrix [15431068] (imputed) 3 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200704 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylmalonate levels 8,172 European ancestry individuals NA Affymetrix [15427723] (imputed) 5 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90200705 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Biliverdin levels 8,262 European ancestry individuals NA Affymetrix [15431108] (imputed) 2 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90200706 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine levels 8,262 European ancestry individuals NA Affymetrix [15431296] (imputed) 2 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90200707 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12112 levels 8,211 European ancestry individuals NA Affymetrix [15429523] (imputed) 7 X-12112 measurement http://www.ebi.ac.uk/efo/EFO_0800705 GCST90200708 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12798 levels 8,186 European ancestry individuals NA Affymetrix [15428167] (imputed) 4 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90200709 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-alpha-lysine levels 8,250 European ancestry individuals NA Affymetrix [15430744] (imputed) 1 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90200107 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphingadienine (d18:2/16:0) levels 7,805 European ancestry individuals NA Affymetrix [15411861] (imputed) 0 N-palmitoyl-sphingadienine (d18:2/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800516 GCST90200108 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] levels 7,744 European ancestry individuals NA Affymetrix [15408090] (imputed) 4 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800500 GCST90200109 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoleoylcarnitine (C16:1) levels 8,263 European ancestry individuals NA Affymetrix [15431080] (imputed) 2 palmitoleoylcarnitine (C16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800493 GCST90200110 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingadienine (d18:2/18:0) levels 7,229 European ancestry individuals NA Affymetrix [15385376] (imputed) 1 N-stearoyl-sphingadienine (d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800521 GCST90200111 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-2-methylbutyrate levels 8,018 European ancestry individuals NA Affymetrix [15420922] (imputed) 0 blood 2,3-dihydroxy-2-methylbutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022219 GCST90200112 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcholine levels 7,140 European ancestry individuals NA Affymetrix [15382261] (imputed) 0 stearoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800534 GCST90200113 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-tricosanoyl-sphingadienine (d18:2/23:0) levels 7,274 European ancestry individuals NA Affymetrix [15391817] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90200114 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-heptadecasphingosine (d17:1/16:0) levels 7,141 European ancestry individuals NA Affymetrix [15384116] (imputed) 1 N-palmitoyl-heptadecasphingosine (d17:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800531 GCST90200115 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/14:0, d16:1/16:0) levels 7,270 European ancestry individuals NA Affymetrix [15389419] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90200116 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) levels 8,012 European ancestry individuals NA Affymetrix [15423184] (imputed) 4 glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800533 GCST90200117 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:2/24:1, d18:1/24:2) levels 8,251 European ancestry individuals NA Affymetrix [15430906] (imputed) 2 glycosyl ceramide (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0800532 GCST90200118 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:1/23:1, d17:1/24:1) levels 5,309 European ancestry individuals NA Affymetrix [15269795] (imputed) 2 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90200119 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingadienine levels 4,533 European ancestry individuals NA Affymetrix [15446803] (imputed) 1 sphingadienine measurement http://www.ebi.ac.uk/efo/EFO_0800526 GCST90200120 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/17:0, d17:1/18:0) levels 6,073 European ancestry individuals NA Affymetrix [15328761] (imputed) 1 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90200121 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nisinate (24:6n3) levels 4,765 European ancestry individuals NA Affymetrix [15448045] (imputed) 1 nisinate (24:6n3) measurement http://www.ebi.ac.uk/efo/EFO_0800536 GCST90200122 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/20:0, d16:0/22:0) levels 8,277 European ancestry individuals NA Affymetrix [15431391] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200123 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/24:2) levels 8,140 European ancestry individuals NA Affymetrix [15425672] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200124 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:2/16:0, d18:2/15:0) levels 8,264 European ancestry individuals NA Affymetrix [15431498] (imputed) 2 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200125 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/23:1) levels 8,267 European ancestry individuals NA Affymetrix [15431692] (imputed) 1 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200126 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoylcarnitine (C22) levels 7,368 European ancestry individuals NA Affymetrix [15390084] (imputed) 2 behenoylcarnitine (C22) measurement http://www.ebi.ac.uk/efo/EFO_0800539 GCST90200127 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/18:1) levels 8,253 European ancestry individuals NA Affymetrix [15431191] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200128 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/21:0, d16:2/23:0) levels 8,260 European ancestry individuals NA Affymetrix [15431255] (imputed) 3 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200129 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoylcholine levels 8,193 European ancestry individuals NA Affymetrix [15426246] (imputed) 0 linoleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800535 GCST90200130 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/19:0, d19:1/18:0) levels 8,256 European ancestry individuals NA Affymetrix [15431171] (imputed) 4 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90200131 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine to methionine sulfoxide ratio 8,214 European ancestry individuals NA Affymetrix [15428855] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200760 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrulline to dimethylarginine (SDMA + ADMA) ratio 8,243 European ancestry individuals NA Affymetrix [15429764] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200761 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitate (16:0) to myristate (14:0) ratio 8,215 European ancestry individuals NA Affymetrix [15429583] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200762 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to N-acetylneuraminate ratio 8,256 European ancestry individuals NA Affymetrix [15431018] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200763 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to uridine ratio 8,186 European ancestry individuals NA Affymetrix [15428749] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200764 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to alanine ratio 8,230 European ancestry individuals NA Affymetrix [15430342] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200765 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to phosphoethanolamine ratio 8,205 European ancestry individuals NA Affymetrix [15428290] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200766 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to glucose ratio 8,232 European ancestry individuals NA Affymetrix [15429692] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200767 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to 2'-deoxyuridine ratio 7,846 European ancestry individuals NA Affymetrix [15413441] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200768 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to mannose ratio 8,206 European ancestry individuals NA Affymetrix [15430053] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200769 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylalanine to tyrosine ratio 8,205 European ancestry individuals NA Affymetrix [15429951] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200770 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to fructose ratio 8,209 European ancestry individuals NA Affymetrix [15429388] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200771 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to citrate ratio 8,238 European ancestry individuals NA Affymetrix [15430461] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200772 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine to alpha-tocopherol ratio 8,197 European ancestry individuals NA Affymetrix [15429033] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200773 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Catechol glucuronide levels 4,698 European ancestry individuals NA Affymetrix [15443742] (imputed) 0 catechol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800088 GCST90200096 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Furaneol sulfate levels 5,882 European ancestry individuals NA Affymetrix [15307099] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200097 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/24:1) levels 8,265 European ancestry individuals NA Affymetrix [15431242] (imputed) 5 lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800517 GCST90200098 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-oleoylserine levels 7,591 European ancestry individuals NA Affymetrix [15403094] (imputed) 2 N-oleoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800525 GCST90200099 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanesulfonate (PFOS) levels 8,218 European ancestry individuals NA Affymetrix [15430460] (imputed) 1 perfluorooctanesulfonate (PFOS) measurement http://www.ebi.ac.uk/efo/EFO_0801018 GCST90200100 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) levels 7,837 European ancestry individuals NA Affymetrix [15413386] (imputed) 5 pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800494 GCST90200101 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) levels 7,540 European ancestry individuals NA Affymetrix [15401733] (imputed) 1 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800484 GCST90200102 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] levels 7,731 European ancestry individuals NA Affymetrix [15406515] (imputed) 3 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800499 GCST90200103 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecadienoate (16:2n6) levels 8,274 European ancestry individuals NA Affymetrix [15431231] (imputed) 0 hexadecadienoate (16:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800491 GCST90200104 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) levels 8,232 European ancestry individuals NA Affymetrix [15429546] (imputed) 5 glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800520 GCST90200105 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetylglutamine levels 7,752 European ancestry individuals NA Affymetrix [15413916] (imputed) 1 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90200106 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13431 levels 8,161 European ancestry individuals NA Affymetrix [15427350] (imputed) 3 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90200710 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19141 levels 8,244 European ancestry individuals NA Affymetrix [15430574] (imputed) 4 X-19141 measurement http://www.ebi.ac.uk/efo/EFO_0800799 GCST90200711 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to 5-methylthioadenosine (MTA) ratio 7,320 European ancestry individuals NA Affymetrix [15387635] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200712 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine to ornithine ratio 7,309 European ancestry individuals NA Affymetrix [15389885] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200713 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to alpha-ketobutyrate ratio 8,216 European ancestry individuals NA Affymetrix [15429621] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200714 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to glutamate ratio 8,274 European ancestry individuals NA Affymetrix [15431516] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200715 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to phosphoethanolamine ratio 4,579 European ancestry individuals NA Affymetrix [15442905] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200716 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phosphoglycerate to adenosine 5'-diphosphate (ADP) ratio 4,530 European ancestry individuals NA Affymetrix [15439827] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200717 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to succinate ratio 8,260 European ancestry individuals NA Affymetrix [15431142] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200718 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 3',5'-cyclic monophosphate (cAMP) to adenosine 5'-monophosphate (AMP) ratio 6,726 European ancestry individuals NA Affymetrix [15361255] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200719 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to pantothenate ratio 4,561 European ancestry individuals NA Affymetrix [15443741] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200720 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to phosphate ratio 4,559 European ancestry individuals NA Affymetrix [15443646] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200721 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-adenosylhomocysteine (SAH) to leucine ratio 6,122 European ancestry individuals NA Affymetrix [15326660] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200722 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-adenosylhomocysteine (SAH) to 5-methyluridine (ribothymidine) ratio 6,078 European ancestry individuals NA Affymetrix [15324362] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200723 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate to taurocholate ratio 7,328 European ancestry individuals NA Affymetrix [15395924] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200724 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to creatine ratio 4,561 European ancestry individuals NA Affymetrix [15443600] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200725 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylputrescine to (N(1) + N(8))-acetylspermidine ratio 8,144 European ancestry individuals NA Affymetrix [15428347] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200726 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 3',5'-cyclic monophosphate (cAMP) to taurocholate ratio 6,329 European ancestry individuals NA Affymetrix [15339135] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200727 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to Adenosine 5'-monophosphate (AMP) ratio 4,573 European ancestry individuals NA Affymetrix [15443752] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200728 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phosphoglycerate to phosphate ratio 8,153 European ancestry individuals NA Affymetrix [15428088] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200729 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to fructose ratio 4,571 European ancestry individuals NA Affymetrix [15444048] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200730 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to mannose ratio 4,587 European ancestry individuals NA Affymetrix [15445078] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200731 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to tyrosine ratio 4,560 European ancestry individuals NA Affymetrix [15443680] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200732 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to N-acetylglucosamine to N-acetylgalactosamine ratio 4,392 European ancestry individuals NA Affymetrix [15435460] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200733 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to palmitate (16:0) ratio 8,227 European ancestry individuals NA Affymetrix [15430401] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200734 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine to ornithine ratio 8,250 European ancestry individuals NA Affymetrix [15430990] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200735 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to arginine ratio 4,568 European ancestry individuals NA Affymetrix [15444271] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200736 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to 2'-deoxyuridine ratio 4,391 European ancestry individuals NA Affymetrix [15430579] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200737 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to inosine 5'-monophosphate (IMP) ratio 4,601 European ancestry individuals NA Affymetrix [15454332] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200738 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to proline ratio 8,190 European ancestry individuals NA Affymetrix [15429560] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200739 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) to oleate to vaccenate (18:1) ratio 8,171 European ancestry individuals NA Affymetrix [15428431] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200740 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to alanine ratio 8,172 European ancestry individuals NA Affymetrix [15429217] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200741 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate to citrate ratio 8,191 European ancestry individuals NA Affymetrix [15428585] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200742 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine to citrulline ratio 8,192 European ancestry individuals NA Affymetrix [15428565] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200743 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine to glutamate ratio 8,194 European ancestry individuals NA Affymetrix [15429237] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200744 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to phenylalanine ratio 8,189 European ancestry individuals NA Affymetrix [15429622] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200745 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to gluconate ratio 4,540 European ancestry individuals NA Affymetrix [15442261] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200746 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to phosphate ratio 8,184 European ancestry individuals NA Affymetrix [15429480] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200747 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate to glutamate ratio 8,190 European ancestry individuals NA Affymetrix [15428853] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200748 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) to pyruvate ratio 8,200 European ancestry individuals NA Affymetrix [15427843] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200749 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate to asparagine ratio 8,195 European ancestry individuals NA Affymetrix [15427409] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200750 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisone to cortisol ratio 8,173 European ancestry individuals NA Affymetrix [15427675] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200751 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinate to acetoacetate ratio 6,829 European ancestry individuals NA Affymetrix [15369335] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200752 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate to citrulline ratio 8,139 European ancestry individuals NA Affymetrix [15427134] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200753 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine to phosphate ratio 8,017 European ancestry individuals NA Affymetrix [15420681] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200754 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine 5'-monophosphate (IMP) to phosphate ratio 4,605 European ancestry individuals NA Affymetrix [15456240] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200755 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine to pyridoxal ratio 8,173 European ancestry individuals NA Affymetrix [15428033] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200756 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine to alanine ratio 8,167 European ancestry individuals NA Affymetrix [15427224] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200757 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine to serine ratio 8,206 European ancestry individuals NA Affymetrix [15429049] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200758 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine to trans-urocanate ratio 8,109 European ancestry individuals NA Affymetrix [15425849] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200759 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 8,253 European ancestry individuals NA Affymetrix [15429840] (imputed) 4 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90200685 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,E) levels 8,263 European ancestry individuals NA Affymetrix [15430594] (imputed) 2 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200686 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamate levels 69 South Asian ancestry individuals NA Affymetrix [4348660] (imputed) 0 phenylacetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800687 GCST90203514 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-3-hydroxybutyrylcarnitine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 (S)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800475 GCST90203515 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800476 GCST90203516 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcholine levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 palmitoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800473 GCST90203517 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800466 GCST90203518 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800453 GCST90203519 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (p-18:0/18:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90203520 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (p-16:0/18:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800440 GCST90203521 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels 104 South Asian ancestry individuals NA Affymetrix [4449812] (imputed) 0 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800464 GCST90203522 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800449 GCST90203523 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dilinoleoyl-GPE (18:2/18:2) levels 96 South Asian ancestry individuals NA Affymetrix [4409518] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203524 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4389656] (imputed) 0 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800443 GCST90203525 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) levels 103 South Asian ancestry individuals NA Affymetrix [4463758] (imputed) 0 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800450 GCST90203526 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) levels 107 South Asian ancestry individuals NA Affymetrix [4389407] (imputed) 0 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800470 GCST90203527 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methylserine levels 104 South Asian ancestry individuals NA Affymetrix [4446991] (imputed) 0 2-methylserine measurement http://www.ebi.ac.uk/efo/EFO_0800087 GCST90203528 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Furaneol sulfate levels 78 South Asian ancestry individuals NA Affymetrix [4370711] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203529 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate glucuronide (1) levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90203530 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinoylcarnitine levels 101 South Asian ancestry individuals NA Affymetrix [4505356] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203531 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenoyl-choline levels 79 South Asian ancestry individuals NA Affymetrix [4312938] (imputed) 0 dihomo-linolenoyl-choline measurement http://www.ebi.ac.uk/efo/EFO_0800481 GCST90203532 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoylcholine levels 92 South Asian ancestry individuals NA Affymetrix [4463415] (imputed) 0 docosahexaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800479 GCST90203533 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-2-methylbutyrate levels 105 South Asian ancestry individuals NA Affymetrix [4441697] (imputed) 0 blood 2,3-dihydroxy-2-methylbutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022219 GCST90203534 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methyluridine levels 102 South Asian ancestry individuals NA Affymetrix [4480134] (imputed) 0 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90203535 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) levels 100 South Asian ancestry individuals NA Affymetrix [4527985] (imputed) 0 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800484 GCST90203536 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methylcytidine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2'-O-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800635 GCST90203537 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcholine levels 106 South Asian ancestry individuals NA Affymetrix [4407693] (imputed) 0 oleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800477 GCST90203538 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 androsterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021117 GCST90201094 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylcarnitine (c4) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90201095 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolepropionate levels 59 African ancestry individuals NA Affymetrix [7487444] (imputed) 0 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90201096 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trigonelline levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90201097 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecanedioate levels 58 African ancestry individuals NA Affymetrix [7518880] (imputed) 0 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90201098 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3-dimethylurate levels 40 African ancestry individuals NA Affymetrix [7143598] (imputed) 0 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90201099 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylxanthine levels 55 African ancestry individuals NA Affymetrix [7604481] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90201100 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltyrosine levels 58 African ancestry individuals NA Affymetrix [7514435] (imputed) 0 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90201101 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylvaline levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90201102 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxylaurate levels 59 African ancestry individuals NA Affymetrix [7495178] (imputed) 0 3-hydroxylaurate measurement http://www.ebi.ac.uk/efo/EFO_0800204 GCST90201103 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxysebacate levels 49 African ancestry individuals NA Affymetrix [7424129] (imputed) 0 3-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800205 GCST90201104 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyhexanoate levels 51 African ancestry individuals NA Affymetrix [7713341] (imputed) 0 5-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800206 GCST90201105 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrylglycine levels 37 African ancestry individuals NA Affymetrix [7429038] (imputed) 0 butyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800208 GCST90201106 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate n3 DPA; 22:5n3 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 docosapentaenoate n3 DPA; 22:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021048 GCST90201107 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-ethylpropionate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90201108 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pro-hydroxy-pro levels 58 African ancestry individuals NA Affymetrix [7511917] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90201109 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylcarnitine (c3) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 propionylcarnitine (C3) measurement http://www.ebi.ac.uk/efo/EFO_0800210 GCST90201110 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylglycine levels 52 African ancestry individuals NA Affymetrix [7684012] (imputed) 0 propionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800207 GCST90201111 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosadienoate (22:2n6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 docosadienoate (22:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800211 GCST90201112 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adrenate (22:4n6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90201113 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90201114 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosatrienoate (22:3n3) levels 51 African ancestry individuals NA Affymetrix [7701453] (imputed) 0 blood 13,16,19-Docosatrienoic acid amount http://purl.obolibrary.org/obo/OBA_2050329 GCST90201115 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-undecenoate (11:1n1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90201116 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristoleate (14:1n5) levels 59 African ancestry individuals NA Affymetrix [7497436] (imputed) 0 myristoleate 14:1n5 measurement http://www.ebi.ac.uk/efo/EFO_0021068 GCST90201117 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-4-imidazoleacetate levels 58 African ancestry individuals NA Affymetrix [7521379] (imputed) 0 1-methyl-4-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800015 GCST90201118 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholate levels 59 African ancestry individuals NA Affymetrix [7496533] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90201730 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5,6-dihydrothymine levels 59 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90201731 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyhippurate (salicylurate) levels 58 African ancestry individuals NA Affymetrix [7522334] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90201732 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate levels 53 African ancestry individuals NA Affymetrix [7644291] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90201733 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleate (18:2n6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90201734 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90201735 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurodeoxycholate levels 48 African ancestry individuals NA Affymetrix [7399667] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90201736 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholic acid levels 56 African ancestry individuals NA Affymetrix [7597882] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90201737 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingosine (d18:1/18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800613 GCST90201738 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetate levels 58 African ancestry individuals NA Affymetrix [7496750] (imputed) 0 4-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800124 GCST90201739 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800608 GCST90201740 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9,10-DiHOME levels 57 African ancestry individuals NA Affymetrix [7546091] (imputed) 0 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90201741 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-gpc (16:0/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90201742 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels 59 African ancestry individuals NA Affymetrix [7498120] (imputed) 0 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800609 GCST90201743 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90201744 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Laurate (12:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90201745 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovalerate levels 59 African ancestry individuals NA Affymetrix [7546954] (imputed) 0 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90201746 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinolinate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90201747 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,n6,n6-trimethyllysine levels 57 African ancestry individuals NA Affymetrix [7533158] (imputed) 0 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90201748 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetaminophen sulfate levels 33 African ancestry individuals NA Affymetrix [7758250] (imputed) 0 4-acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021156 GCST90201749 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Adenosine 5'-monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0021574 GCST90201750 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methylthioadenosine (mta) levels 58 African ancestry individuals NA Affymetrix [7514337] (imputed) 0 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90201751 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosapentaenoate (EPA; 20:5n3) levels 59 African ancestry individuals NA Affymetrix [7496336] (imputed) 0 eicosapentaenoate (EPA; 20:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800616 GCST90201752 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinate levels 57 African ancestry individuals NA Affymetrix [7542666] (imputed) 0 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90201753 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyphenylacetate levels 55 African ancestry individuals NA Affymetrix [7553091] (imputed) 0 2-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800131 GCST90201754 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylaspartate (naa) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetylaspartate (NAA) measurement http://www.ebi.ac.uk/efo/EFO_0800012 GCST90201069 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. DHEAS levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 dehydroepiandrosterone sulphate measurement http://www.ebi.ac.uk/efo/EFO_0007001 GCST90201070 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylphenol sulfate levels 52 African ancestry individuals NA Affymetrix [7803946] (imputed) 0 4-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800942 GCST90201071 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oxalate (ethanedioate) levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90201072 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Iminodiacetate (IDA) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 iminodiacetate (IDA) measurement http://www.ebi.ac.uk/efo/EFO_0800945 GCST90201073 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythritol levels in elite athletes 59 African ancestry individuals NA Affymetrix [7486916] (imputed) 0 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90201074 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoylglycerol (18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800195 GCST90201075 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartronate (hydroxymalonate) levels 59 African ancestry individuals NA Affymetrix [7496282] (imputed) 0 tartronate (hydroxymalonate) measurement http://www.ebi.ac.uk/efo/EFO_0800944 GCST90201076 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxypyridine levels 35 African ancestry individuals NA Affymetrix [7446563] (imputed) 0 blood 2,3-dihydroxypyridine measurement http://www.ebi.ac.uk/efo/EFO_0022199 GCST90201077 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxymyristate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 blood 3-hydroxymyristate measurement http://www.ebi.ac.uk/efo/EFO_0022197 GCST90201078 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxobutyrate levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90201079 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homocitrulline levels 59 African ancestry individuals NA Affymetrix [7533667] (imputed) 0 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90201080 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homoarginine levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 serum homoarginine measurement http://www.ebi.ac.uk/efo/EFO_0005421 GCST90201081 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-linoleoylglycerol (18:2) levels 47 African ancestry individuals NA Affymetrix [7483539] (imputed) 0 2-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800197 GCST90201082 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800198 GCST90201083 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citramalate levels 50 African ancestry individuals NA Affymetrix [7497584] (imputed) 0 blood citramalate measurement http://www.ebi.ac.uk/efo/EFO_0022198 GCST90201084 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. EDTA levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 EDTA measurement http://www.ebi.ac.uk/efo/EFO_0800946 GCST90201085 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Galactonate levels 45 African ancestry individuals NA Affymetrix [7532001] (imputed) 0 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90201086 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglycine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90201087 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonate levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90201088 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylhistidine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90201089 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoylglycerol (18:2) levels 59 African ancestry individuals NA Affymetrix [7517115] (imputed) 0 1-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800199 GCST90201090 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetate levels 59 African ancestry individuals NA Affymetrix [7496282] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90201091 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate levels 50 African ancestry individuals NA Affymetrix [7349033] (imputed) 0 glycolithocholate measurement http://www.ebi.ac.uk/efo/EFO_0800203 GCST90201092 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C4 levels 58 African ancestry individuals NA Affymetrix [7577380] (imputed) 0 butyrylcarnitine (C4) measurement http://www.ebi.ac.uk/efo/EFO_0800201 GCST90201093 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-3-methylglutarate levels 57 African ancestry individuals NA Affymetrix [7550914] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90201705 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-aminoisobutyrate levels 59 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90201706 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90201707 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosaminylasparagine levels 58 African ancestry individuals NA Affymetrix [7496750] (imputed) 0 N-acetylglucosaminylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800151 GCST90201708 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linoleate (20:2n6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90201709 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl ethanolamide levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 oleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800604 GCST90201710 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetoacetate levels 45 African ancestry individuals NA Affymetrix [7503187] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90201711 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamine levels 59 African ancestry individuals NA Affymetrix [7496582] (imputed) 0 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90201712 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ursodeoxycholate levels 44 African ancestry individuals NA Affymetrix [7630297] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90201713 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylhistidine levels 59 African ancestry individuals NA Affymetrix [7496750] (imputed) 0 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90201714 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Choline levels 59 African ancestry individuals NA Affymetrix [7495100] (imputed) 0 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90201715 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylpyruvate levels 51 African ancestry individuals NA Affymetrix [7738836] (imputed) 0 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90201716 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylleucine levels 59 African ancestry individuals NA Affymetrix [7498168] (imputed) 0 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90201717 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxystearate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90201718 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Anthranilate levels 42 African ancestry individuals NA Affymetrix [7725327] (imputed) 0 anthranilate measurement http://www.ebi.ac.uk/efo/EFO_0800123 GCST90201719 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cys-gly, oxidized levels 59 African ancestry individuals NA Affymetrix [7491870] (imputed) 0 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90201720 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90201721 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrate/isobutyrate (4:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 isobutyrate (4:0) measurement http://www.ebi.ac.uk/efo/EFO_0800605 GCST90201722 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylneuraminate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90201723 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90201724 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxytyrosine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90201725 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phosphoglycerate levels 57 African ancestry individuals NA Affymetrix [7592243] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90201726 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homovanillate (hva) levels 42 African ancestry individuals NA Affymetrix [7717362] (imputed) 0 HVA measurement http://www.ebi.ac.uk/efo/EFO_0005131 GCST90201727 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoyl sphingomyelin (d18:1/18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 stearoyl sphingomyelin (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800611 GCST90201728 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-gpc (16:0/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90201729 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycodeoxycholate levels 45 African ancestry individuals NA Affymetrix [7484302] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90201044 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theophylline levels 55 African ancestry individuals NA Affymetrix [7580264] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90201045 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolelactate levels 59 African ancestry individuals NA Affymetrix [7497538] (imputed) 0 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90201046 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Paraxanthine levels in elite athletes 50 African ancestry individuals NA Affymetrix [7308960] (imputed) 0 paraxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021178 GCST90201047 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methyl-2-oxopentanoate levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90201048 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theobromine levels 57 African ancestry individuals NA Affymetrix [7547745] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90201049 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoxyl sulfate levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010502 GCST90201050 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPI (18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800188 GCST90201051 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gentisate levels 55 African ancestry individuals NA Affymetrix [7647739] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90201052 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoate DHA; 22:6n3 levels 59 African ancestry individuals NA Affymetrix [7496336] (imputed) 0 docosahexaenoate DHA; 22:6n3 measurement http://www.ebi.ac.uk/efo/EFO_0021047 GCST90201053 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dipalmitoyl-gpc (16:0/16:0) levels 59 African ancestry individuals NA Affymetrix [7496336] (imputed) 0 1,2-dipalmitoyl-GPC (16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800189 GCST90201054 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine 1-phosphate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90201055 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPS (18:0/18:1) levels 57 African ancestry individuals NA Affymetrix [7541370] (imputed) 0 1-stearoyl-2-oleoyl-GPS (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800187 GCST90201056 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-palmitoyl-gpc (14:0/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800191 GCST90201057 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxyisocaproate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90201058 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,5-anhydroglucitol (1,5-ag) levels 58 African ancestry individuals NA Affymetrix [7521844] (imputed) 0 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90201059 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maleate levels 59 African ancestry individuals NA Affymetrix [7569028] (imputed) 0 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90201060 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800193 GCST90201061 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyoctanoate levels 59 African ancestry individuals NA Affymetrix [7492215] (imputed) 0 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90201062 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerate (i5:0) levels 57 African ancestry individuals NA Affymetrix [7522739] (imputed) 0 isovalerate (i5:0) measurement http://www.ebi.ac.uk/efo/EFO_0800010 GCST90201063 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetylcarnitine levels (Biocrates platform) 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90201064 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcarnitine levels (Metabolon platform) 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90201065 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine s-sulfate levels 59 African ancestry individuals NA Affymetrix [7496282] (imputed) 0 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90201066 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenyllactate (PLA) levels in elite athletes 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90201067 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylcarnitine levels (Biocrates platform) 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90201068 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronate to etiocholanolone glucuronide ratio 7,631 European ancestry individuals NA Affymetrix [15406935] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201019 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Paraxanthine to 5-acetylamino-6-formylamino-3-methyluracil ratio 7,388 European ancestry individuals NA Affymetrix [15396961] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201020 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine levels 58 African ancestry individuals NA Affymetrix [7497436] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90201021 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol 3-phosphate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90201022 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronate levels 57 African ancestry individuals NA Affymetrix [7573386] (imputed) 0 glucuronate measurement http://www.ebi.ac.uk/efo/EFO_0010486 GCST90201023 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxovalerate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90201024 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylhistidine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90201025 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Benzoate levels 49 African ancestry individuals NA Affymetrix [7401847] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90201026 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfoxide levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90201027 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xanthurenate levels 53 African ancestry individuals NA Affymetrix [7687392] (imputed) 0 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90201028 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hippurate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90201029 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetate levels 55 African ancestry individuals NA Affymetrix [7658563] (imputed) 0 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90201030 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Suberate (C8-DC) levels 51 African ancestry individuals NA Affymetrix [7709877] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90201031 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphorylcholine (GPC) levels 59 African ancestry individuals NA Affymetrix [7492232] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90201032 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90201033 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maltotriose levels 33 African ancestry individuals NA Affymetrix [7727163] (imputed) 0 maltotriose measurement http://www.ebi.ac.uk/efo/EFO_0800142 GCST90201034 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phenylpropionate hydrocinnamate levels 57 African ancestry individuals NA Affymetrix [7532966] (imputed) 0 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90201035 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole lactate levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90201036 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartarate levels 54 African ancestry individuals NA Affymetrix [7615140] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90201037 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglutamate levels 54 African ancestry individuals NA Affymetrix [7705505] (imputed) 0 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90201038 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-alpha-acetylornithine levels 42 African ancestry individuals NA Affymetrix [7871192] (imputed) 0 N-alpha-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800006 GCST90201039 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-guanidinobutanoate levels 58 African ancestry individuals NA Affymetrix [7555824] (imputed) 0 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90201040 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxylysine levels 58 African ancestry individuals NA Affymetrix [7550932] (imputed) 0 5-hydroxylysine measurement http://www.ebi.ac.uk/efo/EFO_0800002 GCST90201041 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ribitol levels 59 African ancestry individuals NA Affymetrix [7487444] (imputed) 0 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90201042 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90201043 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearidonate (18:4n3) levels 59 African ancestry individuals NA Affymetrix [7496336] (imputed) 0 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90201119 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sebacate (C10-DC) levels 55 African ancestry individuals NA Affymetrix [7589359] (imputed) 0 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90201120 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hyocholate levels 40 African ancestry individuals NA Affymetrix [7504138] (imputed) 0 hyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800219 GCST90201121 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Epiandrosterone sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90201122 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-dodecenoate (12:1n7) levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 5-dodecenoate 12:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021100 GCST90201123 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201685 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Allantoin levels 59 African ancestry individuals NA Affymetrix [7496805] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90201686 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xanthine levels 59 African ancestry individuals NA Affymetrix [7499364] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90201687 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erucate (22:1n9) levels 59 African ancestry individuals NA Affymetrix [7507886] (imputed) 0 erucate (22:1n9) measurement http://www.ebi.ac.uk/efo/EFO_0800601 GCST90201688 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90201689 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-tocopherol levels 59 African ancestry individuals NA Affymetrix [7496582] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90201690 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylleucine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90201691 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylmethionine levels 58 African ancestry individuals NA Affymetrix [7546644] (imputed) 0 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90201692 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (z,z) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201693 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyisobutyrate levels 59 African ancestry individuals NA Affymetrix [7488508] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90201694 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminobutyrate levels 59 African ancestry individuals NA Affymetrix [7495043] (imputed) 0 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90201695 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-alanine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90201696 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylvaline levels 59 African ancestry individuals NA Affymetrix [7486916] (imputed) 0 N-acetylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800117 GCST90201697 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90201698 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphoethanolamine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90201699 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thyroxine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90201700 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetamidobutanoate levels 58 African ancestry individuals NA Affymetrix [7506653] (imputed) 0 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90201701 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl indole-3-acetate levels 43 African ancestry individuals NA Affymetrix [7607277] (imputed) 0 methyl indole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0801063 GCST90201702 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillylmandelate (VMA) levels 59 African ancestry individuals NA Affymetrix [7506144] (imputed) 0 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90201703 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltyrosine levels 57 African ancestry individuals NA Affymetrix [7558173] (imputed) 0 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90201704 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeic acid sulfate levels 104 South Asian ancestry individuals NA Affymetrix [4445734] (imputed) 0 caffeic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801013 GCST90203539 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 2-sulfate levels 105 South Asian ancestry individuals NA Affymetrix [4431995] (imputed) 0 ascorbic acid 2-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800169 GCST90203540 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoleoylcarnitine (C16:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 palmitoleoylcarnitine (C16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800493 GCST90203541 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonoylcholine levels 106 South Asian ancestry individuals NA Affymetrix [4416479] (imputed) 0 arachidonoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800478 GCST90203542 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanesulfonate (PFOS) levels 107 South Asian ancestry individuals NA Affymetrix [4394451] (imputed) 0 perfluorooctanesulfonate (PFOS) measurement http://www.ebi.ac.uk/efo/EFO_0801018 GCST90203543 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] levels 100 South Asian ancestry individuals NA Affymetrix [4512265] (imputed) 0 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800499 GCST90203544 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] levels 99 South Asian ancestry individuals NA Affymetrix [4318918] (imputed) 0 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800500 GCST90203545 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-alpha-lysine levels 107 South Asian ancestry individuals NA Affymetrix [4394255] (imputed) 0 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90203546 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphingadienine (d18:2/16:0) levels 102 South Asian ancestry individuals NA Affymetrix [4485609] (imputed) 0 N-palmitoyl-sphingadienine (d18:2/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800516 GCST90203547 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/24:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800517 GCST90203548 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) levels 102 South Asian ancestry individuals NA Affymetrix [4487850] (imputed) 0 pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800494 GCST90203549 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructose to maltose ratio 6,307 European ancestry individuals NA Affymetrix [15344259] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201005 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate to 3-methyl-2-oxovalerate ratio 8,136 European ancestry individuals NA Affymetrix [15426159] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201006 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to N-palmitoyl-sphinganine (d18:0 to 16:0) ratio 8,119 European ancestry individuals NA Affymetrix [15426344] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201007 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonine to alpha-ketobutyrate ratio 8,099 European ancestry individuals NA Affymetrix [15425776] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201008 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonine to pyruvate ratio 8,220 European ancestry individuals NA Affymetrix [15428258] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201009 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate to 4-methyl-2-oxopentanoate ratio 8,142 European ancestry individuals NA Affymetrix [15425957] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201010 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxovalerate to 4-methyl-2-oxopentanoate ratio 8,233 European ancestry individuals NA Affymetrix [15429668] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201011 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxovalerate to 3-methyl-2-oxobutyrate ratio 8,200 European ancestry individuals NA Affymetrix [15429510] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201012 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone glucuronide to etiocholanolone glucuronide ratio 7,555 European ancestry individuals NA Affymetrix [15398316] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201013 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronate to androsterone glucuronide ratio 7,804 European ancestry individuals NA Affymetrix [15412106] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201014 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (Z,Z) to androsterone glucuronide ratio 7,888 European ancestry individuals NA Affymetrix [15416763] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201015 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (Z,Z) to etiocholanolone glucuronide ratio 7,707 European ancestry individuals NA Affymetrix [15409950] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201016 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methyl-2-oxopentanoate to 3-methyl-2-oxobutyrate ratio 8,224 European ancestry individuals NA Affymetrix [15430516] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201017 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (Z,Z) to glucuronate ratio 8,103 European ancestry individuals NA Affymetrix [15425649] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201018 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecanedioate (C14-DC) levels 103 East Asian ancestry individuals NA Affymetrix [4298993] (imputed) 0 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90202257 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylphenol sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4299732] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90202258 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90202259 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-ribosyl-imidazoleacetate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90202260 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan betaine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90202261 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPI (16:0) levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 1-palmitoyl-GPI (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800257 GCST90202262 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenate (20:3n3 or n6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90202263 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphoethanolamine levels 103 East Asian ancestry individuals NA Affymetrix [4301041] (imputed) 0 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90202264 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,Z or Z,E) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202265 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyladipate levels 82 East Asian ancestry individuals NA Affymetrix [4325856] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90202266 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyrraline levels 102 East Asian ancestry individuals NA Affymetrix [4320940] (imputed) 0 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90202267 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thymol sulfate levels 99 East Asian ancestry individuals NA Affymetrix [4194196] (imputed) 0 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90202268 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Chiro-inositol levels 64 East Asian ancestry individuals NA Affymetrix [4277953] (imputed) 0 chiro-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800270 GCST90202269 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-cresol sulfate levels 85 East Asian ancestry individuals NA Affymetrix [4264406] (imputed) 0 O-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800955 GCST90202270 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphinganine-1-phosphate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 sphinganine-1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800274 GCST90202271 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylphenylsulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90202272 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-gpc (18:0/20:4) levels 103 East Asian ancestry individuals NA Affymetrix [4301000] (imputed) 0 1-stearoyl-2-arachidonoyl-GPC (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800271 GCST90202273 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPI (18:2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-linoleoyl-GPI (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800266 GCST90202274 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPE (18:0/18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-stearoyl-2-oleoyl-GPE (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800269 GCST90202275 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethylarginine (sdma + adma) levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90202276 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylalanine levels 88 East Asian ancestry individuals NA Affymetrix [4190673] (imputed) 0 gamma-glutamylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800675 GCST90202277 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylphenol sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90202278 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycosyl-N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800275 GCST90202279 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels 103 East Asian ancestry individuals NA Affymetrix [4303764] (imputed) 0 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800272 GCST90202280 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPI (18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-oleoyl-GPI (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800265 GCST90202281 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxycoumarin levels 68 East Asian ancestry individuals NA Affymetrix [4167057] (imputed) 0 4-hydroxycoumarin measurement http://www.ebi.ac.uk/efo/EFO_0800959 GCST90202307 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ergothioneine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90202308 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl sphingomyelin (d18:1/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90202309 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 13-HODE + 9-HODE levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 13-HODE + 9-HODE measurement http://www.ebi.ac.uk/efo/EFO_0800308 GCST90202310 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90202311 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 16a-hydroxy DHEA 3-sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90202312 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cinnamoylglycine levels 79 East Asian ancestry individuals NA Affymetrix [4171040] (imputed) 0 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90202313 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenolone sulfate levels 101 East Asian ancestry individuals NA Affymetrix [4330348] (imputed) 0 pregnenolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800303 GCST90202314 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoylcarnitine (C10:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 cis-4-decenoylcarnitine (C10:1) measurement http://www.ebi.ac.uk/efo/EFO_0800311 GCST90202315 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-3-methylhistidine levels 71 East Asian ancestry individuals NA Affymetrix [4360095] (imputed) 0 N-acetyl-3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800044 GCST90202316 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyhippurate levels 102 East Asian ancestry individuals NA Affymetrix [4317691] (imputed) 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90202317 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylmethionine levels 97 East Asian ancestry individuals NA Affymetrix [4222509] (imputed) 0 S-methylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800042 GCST90202318 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tridecenedioate (C13:1-DC) levels 103 East Asian ancestry individuals NA Affymetrix [4302114] (imputed) 0 tridecenedioate (C13:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800309 GCST90202319 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:1/18:1, d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0022108 GCST90202320 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Andro steroid monosulfate C19H28O6S (1) levels 96 East Asian ancestry individuals NA Affymetrix [4241686] (imputed) 0 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90202321 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-cholesten-3-one levels 81 East Asian ancestry individuals NA Affymetrix [4349687] (imputed) 0 4-cholesten-3-one measurement http://www.ebi.ac.uk/efo/EFO_0800310 GCST90202322 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) monosulfate (2) levels 97 East Asian ancestry individuals NA Affymetrix [4226817] (imputed) 0 androstenediol (3beta,17beta) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800295 GCST90202323 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-beta-alanine levels 103 East Asian ancestry individuals NA Affymetrix [4299351] (imputed) 0 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90202324 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-oxo-retinoic acid levels 96 East Asian ancestry individuals NA Affymetrix [4247222] (imputed) 0 blood 4-oxo-retinoic acid measurement http://www.ebi.ac.uk/efo/EFO_0022216 GCST90202325 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-oxoarginine levels 103 East Asian ancestry individuals NA Affymetrix [4303061] (imputed) 0 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90202326 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutaramate levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 alpha-ketoglutaramate measurement http://www.ebi.ac.uk/efo/EFO_0800046 GCST90202327 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoate (10:1n6) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 cis-4-decenoate (10:1n6) measurement http://www.ebi.ac.uk/efo/EFO_0800318 GCST90202328 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxyisovalerate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90202329 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantoate levels 99 East Asian ancestry individuals NA Affymetrix [4194654] (imputed) 0 blood pantoate measurement http://www.ebi.ac.uk/efo/EFO_0022210 GCST90202330 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2s,3R-dihydroxybutyrate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2s,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800312 GCST90202331 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-palmitoyl-GPC (16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800241 GCST90202232 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxy-3-methylvalerate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-hydroxy-3-methylvalerate measurement http://www.ebi.ac.uk/efo/EFO_0800027 GCST90202233 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPE (16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800245 GCST90202234 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gulonate levels 92 East Asian ancestry individuals NA Affymetrix [4320811] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90202235 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarylcarnitine (c5-dc) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glutarylcarnitine (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800030 GCST90202236 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonoyl-GPE (20:4n6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-arachidonoyl-GPE (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800248 GCST90202237 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonoyl-gpc (20:4n6) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 1-arachidonoyl-GPC (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800234 GCST90202238 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Catechol sulfate levels 102 East Asian ancestry individuals NA Affymetrix [4318700] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90202239 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxypalmitate levels 103 East Asian ancestry individuals NA Affymetrix [4300329] (imputed) 0 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90202240 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C5:1 levels 102 East Asian ancestry individuals NA Affymetrix [4316188] (imputed) 0 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90202241 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPE (18:2) levels 103 East Asian ancestry individuals NA Affymetrix [4303764] (imputed) 0 1-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800247 GCST90202242 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovaleroylcarnitine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 beta-hydroxyisovaleroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800031 GCST90202243 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-palmitoleoyl-GPC (16:1) levels 90 East Asian ancestry individuals NA Affymetrix [4361632] (imputed) 0 2-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800240 GCST90202244 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioate levels 103 East Asian ancestry individuals NA Affymetrix [4301452] (imputed) 0 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90202245 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecanedioate (C16-DC) levels 103 East Asian ancestry individuals NA Affymetrix [4301452] (imputed) 0 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90202246 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetylglutamine levels 58 East Asian ancestry individuals NA Affymetrix [4194088] (imputed) 0 indoleacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800035 GCST90202247 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxycaproate levels 69 East Asian ancestry individuals NA Affymetrix [4151376] (imputed) 0 alpha-hydroxycaproate measurement http://www.ebi.ac.uk/efo/EFO_0800261 GCST90202248 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurolithocholate 3-sulfate levels 96 East Asian ancestry individuals NA Affymetrix [4244496] (imputed) 0 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90202249 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-aspartyl-glutamate (naag) levels 100 East Asian ancestry individuals NA Affymetrix [4346589] (imputed) 0 N-acetyl-aspartyl-glutamate (NAAG) measurement http://www.ebi.ac.uk/efo/EFO_0800033 GCST90202250 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-hydroxyphenyl)propionate levels 94 East Asian ancestry individuals NA Affymetrix [4292401] (imputed) 0 3-(3-hydroxyphenyl)propionate measurement http://www.ebi.ac.uk/efo/EFO_0800952 GCST90202251 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycarnitine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90202252 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannitol/sorbitol levels 103 East Asian ancestry individuals NA Affymetrix [4299170] (imputed) 0 sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0010533 GCST90202253 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-acetyllysine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90202254 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylglutamine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 hexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800262 GCST90202255 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,4-dihydroxybutyrate levels 102 East Asian ancestry individuals NA Affymetrix [4320097] (imputed) 0 blood 3,4-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022215 GCST90202256 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylserine levels 102 East Asian ancestry individuals NA Affymetrix [4317398] (imputed) 0 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90202282 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinylcarnitine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90202283 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (E,E) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202284 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17alpha-diol disulfate levels 97 East Asian ancestry individuals NA Affymetrix [4225924] (imputed) 0 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90202285 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17beta-diol disulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90202286 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20alpha-diol disulfate levels 102 East Asian ancestry individuals NA Affymetrix [4320226] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90202287 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylproline levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90202288 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17alpha-diol monosulfate levels 94 East Asian ancestry individuals NA Affymetrix [4278502] (imputed) 0 5alpha-androstan-3alpha,17alpha-diol monosulfate measurement http://www.ebi.ac.uk/efo/EFO_0800283 GCST90202289 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol disulfate (C21H34O8S2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 pregnenediol disulfate (C21H34O8S2) measurement http://www.ebi.ac.uk/efo/EFO_0800279 GCST90202290 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholenate sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300329] (imputed) 0 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90202291 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 21-hydroxypregnenolone disulfate levels 101 East Asian ancestry individuals NA Affymetrix [4331101] (imputed) 0 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90202292 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-diol disulfate levels 72 East Asian ancestry individuals NA Affymetrix [4316865] (imputed) 0 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90202293 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotenoid levels (cryptoxanthin) 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 cryptoxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007897 GCST90202294 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) disulfate (1) levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 androstenediol (3beta,17beta) disulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800278 GCST90202295 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels 102 East Asian ancestry individuals NA Affymetrix [4318892] (imputed) 0 5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800284 GCST90202296 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) disulfate (2) levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 androstenediol (3beta,17beta) disulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800280 GCST90202297 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) levels 101 East Asian ancestry individuals NA Affymetrix [4336964] (imputed) 0 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800285 GCST90202298 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholenate sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90202299 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels 98 East Asian ancestry individuals NA Affymetrix [4213153] (imputed) 0 5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800291 GCST90202300 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3alpha, 17alpha) monosulfate (3) levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 androstenediol (3alpha, 17alpha) monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0800293 GCST90202301 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol disulfate levels 86 East Asian ancestry individuals NA Affymetrix [4244258] (imputed) 0 5alpha-androstan-3alpha,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800287 GCST90202302 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels 102 East Asian ancestry individuals NA Affymetrix [4321471] (imputed) 0 5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800288 GCST90202303 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) monosulfate (1) levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 androstenediol (3beta,17beta) monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800294 GCST90202304 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyglutarate levels 97 East Asian ancestry individuals NA Affymetrix [4228191] (imputed) 0 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90202305 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol sulfate (C21H34O5S) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 pregnenediol sulfate (C21H34O5S) measurement http://www.ebi.ac.uk/efo/EFO_0800299 GCST90202306 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutaconate levels 101 East Asian ancestry individuals NA Affymetrix [4335262] (imputed) 0 3-methylglutaconate measurement http://www.ebi.ac.uk/efo/EFO_0800047 GCST90202332 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Formiminoglutamate levels 103 East Asian ancestry individuals NA Affymetrix [4301972] (imputed) 0 formiminoglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800050 GCST90202333 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90202334 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (16 or 17)-methylstearate (a19:0 or i19:0) levels 103 East Asian ancestry individuals NA Affymetrix [4302736] (imputed) 0 (16 or 17)-methylstearate (a19:0 or i19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800313 GCST90202335 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine disulfide levels 101 East Asian ancestry individuals NA Affymetrix [4333593] (imputed) 0 cysteinylglycine disulfide measurement http://www.ebi.ac.uk/efo/EFO_0800049 GCST90202336 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxy-2-oxoglutaric acid levels 101 East Asian ancestry individuals NA Affymetrix [4337203] (imputed) 0 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90202337 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine levels 102 East Asian ancestry individuals NA Affymetrix [4320243] (imputed) 0 S-methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800054 GCST90202338 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoursodeoxycholate levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 isoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800315 GCST90202339 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyglutamate levels 94 East Asian ancestry individuals NA Affymetrix [4279598] (imputed) 0 4-hydroxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800052 GCST90202340 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydantoin-5-propionate levels 101 East Asian ancestry individuals NA Affymetrix [4333397] (imputed) 0 hydantoin-5-propionate measurement http://www.ebi.ac.uk/efo/EFO_0800051 GCST90202341 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androsterone glucuronide levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 androsterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800317 GCST90202342 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Argininate levels 103 East Asian ancestry individuals NA Affymetrix [4299444] (imputed) 0 argininate measurement http://www.ebi.ac.uk/efo/EFO_0800055 GCST90202343 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12283 levels 95 South Asian ancestry individuals NA Affymetrix [4452909] (imputed) 0 X-12283 measurement http://www.ebi.ac.uk/efo/EFO_0800713 GCST90203908 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12407 levels 79 South Asian ancestry individuals NA Affymetrix [4324407] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90203909 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12410 levels 91 South Asian ancestry individuals NA Affymetrix [4523570] (imputed) 0 X-12410 measurement http://www.ebi.ac.uk/efo/EFO_0800715 GCST90203910 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12544 levels 97 South Asian ancestry individuals NA Affymetrix [4399879] (imputed) 0 X-12544 measurement http://www.ebi.ac.uk/efo/EFO_0021315 GCST90203911 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12680 levels 107 South Asian ancestry individuals NA Affymetrix [4393796] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90203912 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12462 levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 X-12462 measurement http://www.ebi.ac.uk/efo/EFO_0800717 GCST90203913 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12701 levels 89 South Asian ancestry individuals NA Affymetrix [4326638] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203914 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12707 levels 96 South Asian ancestry individuals NA Affymetrix [4431037] (imputed) 0 X-12707 measurement http://www.ebi.ac.uk/efo/EFO_0800720 GCST90203915 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12729 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90203916 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12738 levels 58 South Asian ancestry individuals NA Affymetrix [4309627] (imputed) 0 X-12738 measurement http://www.ebi.ac.uk/efo/EFO_0800726 GCST90203917 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12714 levels 92 South Asian ancestry individuals NA Affymetrix [4506910] (imputed) 0 X-12714 measurement http://www.ebi.ac.uk/efo/EFO_0800722 GCST90203918 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12798 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90203919 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12740 levels 90 South Asian ancestry individuals NA Affymetrix [4525281] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90203920 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16580 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90203946 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17346 levels 73 South Asian ancestry individuals NA Affymetrix [4509570] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203947 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17328 levels 101 South Asian ancestry individuals NA Affymetrix [4514630] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203948 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17335 levels 103 South Asian ancestry individuals NA Affymetrix [4467729] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90203949 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15486 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90203950 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16935 levels 106 South Asian ancestry individuals NA Affymetrix [4413413] (imputed) 0 X-16935 measurement http://www.ebi.ac.uk/efo/EFO_0800763 GCST90203951 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17351 levels 93 South Asian ancestry individuals NA Affymetrix [4495073] (imputed) 0 X-17351 measurement http://www.ebi.ac.uk/efo/EFO_0800774 GCST90203952 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16124 levels 79 South Asian ancestry individuals NA Affymetrix [4324756] (imputed) 0 X-16124 measurement http://www.ebi.ac.uk/efo/EFO_0800757 GCST90203953 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16397 levels 106 South Asian ancestry individuals NA Affymetrix [4407597] (imputed) 0 X-16397 measurement http://www.ebi.ac.uk/efo/EFO_0800758 GCST90203954 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15461 levels 106 South Asian ancestry individuals NA Affymetrix [4411406] (imputed) 0 X-15461 measurement http://www.ebi.ac.uk/efo/EFO_0800749 GCST90203955 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-14939 levels 107 South Asian ancestry individuals NA Affymetrix [4394451] (imputed) 0 X-14939 measurement http://www.ebi.ac.uk/efo/EFO_0800747 GCST90203956 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16087 levels 96 South Asian ancestry individuals NA Affymetrix [4393661] (imputed) 0 X-16087 measurement http://www.ebi.ac.uk/efo/EFO_0800756 GCST90203957 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17357 levels 103 South Asian ancestry individuals NA Affymetrix [4460394] (imputed) 0 X-17357 measurement http://www.ebi.ac.uk/efo/EFO_0800777 GCST90203958 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13866 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90203959 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18922 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-18922 measurement http://www.ebi.ac.uk/efo/EFO_0800797 GCST90203960 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18921 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-18921 measurement http://www.ebi.ac.uk/efo/EFO_0800796 GCST90203961 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17653 levels 102 South Asian ancestry individuals NA Affymetrix [4494868] (imputed) 0 X-17653 measurement http://www.ebi.ac.uk/efo/EFO_0800783 GCST90203962 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17654 levels 98 South Asian ancestry individuals NA Affymetrix [4353293] (imputed) 0 X-17654 measurement http://www.ebi.ac.uk/efo/EFO_0800784 GCST90203963 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21312 levels 57 South Asian ancestry individuals NA Affymetrix [4366464] (imputed) 0 X-21312 measurement http://www.ebi.ac.uk/efo/EFO_0800806 GCST90203964 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21258 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-21258 measurement http://www.ebi.ac.uk/efo/EFO_0800802 GCST90203965 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18901 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-18901 measurement http://www.ebi.ac.uk/efo/EFO_0800794 GCST90203966 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19299 levels 83 South Asian ancestry individuals NA Affymetrix [4469757] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203967 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21319 levels 105 South Asian ancestry individuals NA Affymetrix [4433867] (imputed) 0 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90203968 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21285 levels 84 South Asian ancestry individuals NA Affymetrix [4444940] (imputed) 0 X-21285 measurement http://www.ebi.ac.uk/efo/EFO_0800803 GCST90203969 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18887 levels 87 South Asian ancestry individuals NA Affymetrix [4379706] (imputed) 0 X-18887 measurement http://www.ebi.ac.uk/efo/EFO_0800791 GCST90203970 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12818 levels 85 South Asian ancestry individuals NA Affymetrix [4428483] (imputed) 0 X-12818 measurement http://www.ebi.ac.uk/efo/EFO_0800729 GCST90203921 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12731 levels 67 South Asian ancestry individuals NA Affymetrix [4391588] (imputed) 0 X-12731 measurement http://www.ebi.ac.uk/efo/EFO_0800725 GCST90203922 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12812 levels 84 South Asian ancestry individuals NA Affymetrix [4466690] (imputed) 0 X-12812 measurement http://www.ebi.ac.uk/efo/EFO_0800728 GCST90203923 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12730 levels 83 South Asian ancestry individuals NA Affymetrix [4481673] (imputed) 0 X-12730 measurement http://www.ebi.ac.uk/efo/EFO_0800724 GCST90203924 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12822 levels 102 South Asian ancestry individuals NA Affymetrix [4477993] (imputed) 0 X-12822 measurement http://www.ebi.ac.uk/efo/EFO_0800730 GCST90203925 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12839 levels 63 South Asian ancestry individuals NA Affymetrix [4443188] (imputed) 0 X-12839 measurement http://www.ebi.ac.uk/efo/EFO_0800731 GCST90203926 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12844 levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90203927 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12847 levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90203928 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12906 levels 102 South Asian ancestry individuals NA Affymetrix [4490301] (imputed) 0 X-12906 measurement http://www.ebi.ac.uk/efo/EFO_0800733 GCST90203929 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13431 levels 106 South Asian ancestry individuals NA Affymetrix [4411454] (imputed) 0 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90203930 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13007 levels 85 South Asian ancestry individuals NA Affymetrix [4418799] (imputed) 0 X-13007 measurement http://www.ebi.ac.uk/efo/EFO_0800734 GCST90203931 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12849 levels 99 South Asian ancestry individuals NA Affymetrix [4343065] (imputed) 0 X-12849 measurement http://www.ebi.ac.uk/efo/EFO_0800732 GCST90203932 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13729 levels 98 South Asian ancestry individuals NA Affymetrix [4373940] (imputed) 0 X-13729 measurement http://www.ebi.ac.uk/efo/EFO_0800742 GCST90203933 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12830 levels 63 South Asian ancestry individuals NA Affymetrix [4518826] (imputed) 0 X-12830 measurement http://www.ebi.ac.uk/efo/EFO_0021337 GCST90203934 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13507 levels 104 South Asian ancestry individuals NA Affymetrix [4456898] (imputed) 0 X-13507 measurement http://www.ebi.ac.uk/efo/EFO_0800736 GCST90203935 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13684 levels 106 South Asian ancestry individuals NA Affymetrix [4415575] (imputed) 0 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90203936 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13723 levels 62 South Asian ancestry individuals NA Affymetrix [4510155] (imputed) 0 X-13723 measurement http://www.ebi.ac.uk/efo/EFO_0800739 GCST90203937 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13728 levels 99 South Asian ancestry individuals NA Affymetrix [4349287] (imputed) 0 X-13728 measurement http://www.ebi.ac.uk/efo/EFO_0800741 GCST90203938 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13695 levels 81 South Asian ancestry individuals NA Affymetrix [4521959] (imputed) 0 X-13695 measurement http://www.ebi.ac.uk/efo/EFO_0800738 GCST90203939 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16964 levels 105 South Asian ancestry individuals NA Affymetrix [4435340] (imputed) 0 X-16964 measurement http://www.ebi.ac.uk/efo/EFO_0020011 GCST90203940 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17146 levels 104 South Asian ancestry individuals NA Affymetrix [4445255] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203941 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15523 levels 107 South Asian ancestry individuals NA Affymetrix [4394305] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203942 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17325 levels 88 South Asian ancestry individuals NA Affymetrix [4356492] (imputed) 0 X-17325 measurement http://www.ebi.ac.uk/efo/EFO_0800771 GCST90203943 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15728 levels 99 South Asian ancestry individuals NA Affymetrix [4362972] (imputed) 0 X-15728 measurement http://www.ebi.ac.uk/efo/EFO_0020024 GCST90203944 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13844 levels 92 South Asian ancestry individuals NA Affymetrix [4519295] (imputed) 0 X-13844 measurement http://www.ebi.ac.uk/efo/EFO_0800744 GCST90203945 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21796 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-21796 measurement http://www.ebi.ac.uk/efo/EFO_0800825 GCST90203996 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21834 levels 99 South Asian ancestry individuals NA Affymetrix [4354317] (imputed) 0 X-21834 measurement http://www.ebi.ac.uk/efo/EFO_0800833 GCST90203997 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21829 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-21829 measurement http://www.ebi.ac.uk/efo/EFO_0800830 GCST90203998 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21742 levels 71 South Asian ancestry individuals NA Affymetrix [4535138] (imputed) 0 X-21742 measurement http://www.ebi.ac.uk/efo/EFO_0800823 GCST90203999 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22771 levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 X-22771 measurement http://www.ebi.ac.uk/efo/EFO_0800844 GCST90204000 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22776 levels 91 South Asian ancestry individuals NA Affymetrix [4510361] (imputed) 0 X-22776 measurement http://www.ebi.ac.uk/efo/EFO_0800845 GCST90204001 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23276 levels 68 South Asian ancestry individuals NA Affymetrix [4330326] (imputed) 0 X-23276 measurement http://www.ebi.ac.uk/efo/EFO_0800847 GCST90204002 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22520 levels 60 South Asian ancestry individuals NA Affymetrix [4601076] (imputed) 0 X-22520 measurement http://www.ebi.ac.uk/efo/EFO_0800843 GCST90204003 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22162 levels 107 South Asian ancestry individuals NA Affymetrix [4392753] (imputed) 0 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90204004 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23587 levels 95 South Asian ancestry individuals NA Affymetrix [4426710] (imputed) 0 X-23587 measurement http://www.ebi.ac.uk/efo/EFO_0800849 GCST90204005 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22834 levels 75 South Asian ancestry individuals NA Affymetrix [4446731] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204006 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23636 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-23636 measurement http://www.ebi.ac.uk/efo/EFO_0800852 GCST90204007 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23654 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204008 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23648 levels 89 South Asian ancestry individuals NA Affymetrix [4305222] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204009 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23639 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90204010 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23641 levels 82 South Asian ancestry individuals NA Affymetrix [4503969] (imputed) 0 X-23641 measurement http://www.ebi.ac.uk/efo/EFO_0800854 GCST90204011 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23678 levels 72 South Asian ancestry individuals NA Affymetrix [4485202] (imputed) 0 X-23678 measurement http://www.ebi.ac.uk/efo/EFO_0800861 GCST90204012 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23680 levels 107 South Asian ancestry individuals NA Affymetrix [4396325] (imputed) 0 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90204013 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23665 levels 106 South Asian ancestry individuals NA Affymetrix [4410077] (imputed) 0 X-23665 measurement http://www.ebi.ac.uk/efo/EFO_0800859 GCST90204014 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23659 levels 106 South Asian ancestry individuals NA Affymetrix [4410128] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204015 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23655 levels 63 South Asian ancestry individuals NA Affymetrix [4456492] (imputed) 0 X-23655 measurement http://www.ebi.ac.uk/efo/EFO_0800856 GCST90204016 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23739 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90204017 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23782 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-23782 measurement http://www.ebi.ac.uk/efo/EFO_0800865 GCST90204018 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23780 levels 104 South Asian ancestry individuals NA Affymetrix [4446889] (imputed) 0 X-23780 measurement http://www.ebi.ac.uk/efo/EFO_0800864 GCST90204019 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24306 levels 107 South Asian ancestry individuals NA Affymetrix [4394792] (imputed) 0 X-24306 measurement http://www.ebi.ac.uk/efo/EFO_0800870 GCST90204020 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17367 levels 60 South Asian ancestry individuals NA Affymetrix [4572250] (imputed) 0 X-17367 measurement http://www.ebi.ac.uk/efo/EFO_0800779 GCST90203971 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17685 levels 99 South Asian ancestry individuals NA Affymetrix [4339657] (imputed) 0 X-17685 measurement http://www.ebi.ac.uk/efo/EFO_0800786 GCST90203972 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18888 levels 87 South Asian ancestry individuals NA Affymetrix [4386291] (imputed) 0 X-18888 measurement http://www.ebi.ac.uk/efo/EFO_0800792 GCST90203973 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18886 levels 104 South Asian ancestry individuals NA Affymetrix [4448943] (imputed) 0 X-18886 measurement http://www.ebi.ac.uk/efo/EFO_0800790 GCST90203974 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18913 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-18913 measurement http://www.ebi.ac.uk/efo/EFO_0800795 GCST90203975 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18779 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203976 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17676 levels 102 South Asian ancestry individuals NA Affymetrix [4494410] (imputed) 0 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90203977 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17438 levels 76 South Asian ancestry individuals NA Affymetrix [4383828] (imputed) 0 X-17438 measurement http://www.ebi.ac.uk/efo/EFO_0800781 GCST90203978 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21310 levels 100 South Asian ancestry individuals NA Affymetrix [4533796] (imputed) 0 X-21310 measurement http://www.ebi.ac.uk/efo/EFO_0800805 GCST90203979 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21733 levels 77 South Asian ancestry individuals NA Affymetrix [4350276] (imputed) 0 X-21733 measurement http://www.ebi.ac.uk/efo/EFO_0800820 GCST90203980 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21441 levels 103 South Asian ancestry individuals NA Affymetrix [4468013] (imputed) 0 X-21441 measurement http://www.ebi.ac.uk/efo/EFO_0800814 GCST90203981 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21383 levels 103 South Asian ancestry individuals NA Affymetrix [4469748] (imputed) 0 X-21383 measurement http://www.ebi.ac.uk/efo/EFO_0800812 GCST90203982 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21442 levels 73 South Asian ancestry individuals NA Affymetrix [4460794] (imputed) 0 X-21442 measurement http://www.ebi.ac.uk/efo/EFO_0800815 GCST90203983 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21353 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-21353 measurement http://www.ebi.ac.uk/efo/EFO_0800809 GCST90203984 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21339 levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 X-21339 measurement http://www.ebi.ac.uk/efo/EFO_0800808 GCST90203985 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21355 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-21355 measurement http://www.ebi.ac.uk/efo/EFO_0800810 GCST90203986 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21607 levels 103 South Asian ancestry individuals NA Affymetrix [4469520] (imputed) 0 X-21607 measurement http://www.ebi.ac.uk/efo/EFO_0800819 GCST90203987 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21471 levels 107 South Asian ancestry individuals NA Affymetrix [4397310] (imputed) 0 X-21471 measurement http://www.ebi.ac.uk/efo/EFO_0800818 GCST90203988 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21470 levels 103 South Asian ancestry individuals NA Affymetrix [4461846] (imputed) 0 X-21470 measurement http://www.ebi.ac.uk/efo/EFO_0800817 GCST90203989 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21364 levels 105 South Asian ancestry individuals NA Affymetrix [4423040] (imputed) 0 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90203990 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21467 levels 106 South Asian ancestry individuals NA Affymetrix [4408844] (imputed) 0 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90203991 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21752 levels 66 South Asian ancestry individuals NA Affymetrix [4409577] (imputed) 0 X-21752 measurement http://www.ebi.ac.uk/efo/EFO_0800824 GCST90203992 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21807 levels 73 South Asian ancestry individuals NA Affymetrix [4487207] (imputed) 0 X-21807 measurement http://www.ebi.ac.uk/efo/EFO_0800827 GCST90203993 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21736 levels 107 South Asian ancestry individuals NA Affymetrix [4390812] (imputed) 0 X-21736 measurement http://www.ebi.ac.uk/efo/EFO_0800821 GCST90203994 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21821 levels 96 South Asian ancestry individuals NA Affymetrix [4428012] (imputed) 0 X-21821 measurement http://www.ebi.ac.uk/efo/EFO_0800829 GCST90203995 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1534) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278800 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1538) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278801 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1545) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278802 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1584) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278807 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1590) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278808 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1593) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278809 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1596) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278810 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1610) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278811 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1616) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278812 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1619) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278813 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1637) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278814 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1645) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278815 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1650) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278816 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1658) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278817 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1664) (311-dihydroxy-tetradecanoic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of Ipurolic acid in blood serum http://purl.obolibrary.org/obo/OBA_2045051 GCST90278818 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1668) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278819 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1670) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278820 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1672) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278821 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1673) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278822 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1687) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278823 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1690) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278824 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1692) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278825 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1693) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 83 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278826 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1694) ((1R2R)-3-(12-Dihydro-2-hydroxy-1-naphthalenyl)thio-2-oxopropanoic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 (1R2R)-3-(12-dihydro-2-hydroxy-1-naphthalenyl)thio-2-oxopropanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0803468 GCST90278827 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1703) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278828 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1704) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278829 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1707) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278830 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1709) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278831 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1717) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278832 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1723) (Tiadinil) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tiadinil measurement http://www.ebi.ac.uk/efo/EFO_0803519 GCST90278833 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1731) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278834 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1737) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278835 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1739) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278836 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1761) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278837 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1770) (Mercuric chloride) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 mercuric chloride measurement http://www.ebi.ac.uk/efo/EFO_0022068 GCST90278838 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1773) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278839 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1790) (S-(4-Bromophenyl)-mercaptopyruvate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 S-(4-bromophenyl)-mercaptopyruvate measurement http://www.ebi.ac.uk/efo/EFO_0803513 GCST90278840 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1796) (Bakers yeast extract) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 bakers yeast extract measurement http://www.ebi.ac.uk/efo/EFO_0803404 GCST90278841 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1811) (19-Noretiocholanolone) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278842 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1817) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278843 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_182) (Glyceric acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 glyceric acid measurement http://www.ebi.ac.uk/efo/EFO_0801163 GCST90278844 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1825) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278845 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1834) (Alpha-Linolenic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 alpha-linolenic acid measurement http://www.ebi.ac.uk/efo/EFO_0007759 GCST90278846 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1840) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278847 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_185) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278848 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1850) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278849 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2242) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278910 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2254) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278911 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2257) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278912 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2264) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278913 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1285) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278750 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_129) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278751 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1297) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278752 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1310) (Chloromethiuron) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 20 chloromethiuron measurement http://www.ebi.ac.uk/efo/EFO_0803488 GCST90278753 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1317) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278754 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1322) (2-Chloro-45-xylyl N-hydroxy-N-methylcarbamate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 2-chloro-45-xylyl N-hydroxy-N-methylcarbamate measurement http://www.ebi.ac.uk/efo/EFO_0803523 GCST90278755 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1323) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278756 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1337) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278757 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1351) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278758 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1354) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 19 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278759 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1368) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278760 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1376) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278761 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1379) (1-Methoxypyrene) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278762 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1383) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278763 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_139) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278764 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1393) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278765 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1394) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278766 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1395) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278767 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1399) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278768 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1401) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278769 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1405) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278770 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1407) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278771 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1408) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 15 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278772 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1412) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278773 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_142) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278774 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3875) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279225 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_388) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 15 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279226 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3886) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279227 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3887) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279228 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3888) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279229 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_389) (Ornithine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90279230 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3892) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279231 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3898) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279232 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_39) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279233 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3900) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279234 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3911) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279235 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3914) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279236 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3925) ((5Z7E)-(3S)-262626272727-hexafluoro-910-seco-5710(19)16-cholestatetraen-23-yne-325-diol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 vitamin D metabolic process quality http://purl.obolibrary.org/obo/OBA_1000312 GCST90279237 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3928) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279238 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_393) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279239 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3932) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279240 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1003) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278687 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1006) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278688 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1547) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278803 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1550) (Bis(methylsulfonylmethyl) disulfide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 bis(methylsulfonylmethyl) disulfide measurement http://www.ebi.ac.uk/efo/EFO_0803405 GCST90278804 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1570) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278805 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1574) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278806 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1273) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278747 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1277) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278748 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1284) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278749 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2696) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279920 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2702) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279921 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_271) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279922 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2713) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279923 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2716) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279924 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2718) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279925 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_273) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279926 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2730) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279927 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2736) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279928 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2750) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279929 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2751) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279930 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2752) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279931 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2755) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279932 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2756) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279933 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2759) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279934 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2769) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279935 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_277) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279936 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2774) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279937 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2781) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279938 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2793) (68-Dimethyl-67-didehydroergoline) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 68-dimethyl-67-didehydroergoline measurement http://www.ebi.ac.uk/efo/EFO_0803478 GCST90279939 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2797) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279940 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2798) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279941 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_280) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279942 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2802) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279943 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2809) (Anserine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 anserine measurement http://www.ebi.ac.uk/efo/EFO_0803402 GCST90279944 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2546) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279895 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2550) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279896 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2558) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279897 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2573) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279898 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2575) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279899 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2577) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279900 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2579) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279901 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2611) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279902 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2613) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279903 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2626) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279904 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2628) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279905 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_263) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279906 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2634) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279907 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2635) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279908 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2640) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279909 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2644) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279910 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2650) (Di-2-thienyl disulfide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 di-2-thienyl disulfide measurement http://www.ebi.ac.uk/efo/EFO_0803412 GCST90279911 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2660) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279912 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2661) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279913 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2662) (Butyrylcarnitine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 butyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020010 GCST90279914 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2668) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279915 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2677) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279916 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2680) (Isobutyryl-L-carnitine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279917 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2685) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279918 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2691) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279919 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2810) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279945 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_282) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279946 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2822) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279947 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2823) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279948 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2824) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279949 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2826) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279950 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3642) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279181 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3648) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279182 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3650) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279183 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3653) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279184 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3659) (alpha-D-Ribose 1-methylphosphonate 5-triphosphate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 alpha-D-ribose 1-methylphosphonate 5-triphosphate measurement http://www.ebi.ac.uk/efo/EFO_0803481 GCST90279185 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3666) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279186 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3669) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279187 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3673) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279188 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3675) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279189 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3678) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279190 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3682) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279191 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_369) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279192 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3695) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279193 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3707) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279194 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3710) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279195 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3715) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279196 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3716) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279197 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_372) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279198 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3725) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279199 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1420) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278775 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1426) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278776 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1431) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278777 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1436) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278778 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1441) (Benzyl cinnamate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278779 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1448) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278780 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1456) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278781 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1460) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278782 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1463) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278783 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1476) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278784 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1486) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278785 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1488) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278786 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1493) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278787 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1494) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278788 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1499) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278789 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_150) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278790 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1500) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278791 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1507) (5-Sulfo-13-benzenedicarboxylic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 5-sulfo-13-benzenedicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0803396 GCST90278792 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1509) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278793 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_151) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278794 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1514) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278795 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1516) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278796 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1517) (N-Phosphotaurocyamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278797 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1527) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278798 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1532) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278799 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3730) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279200 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3739) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279201 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3755) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279202 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3758) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279203 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3759) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279204 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3761) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279205 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3773) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279206 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3776) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279207 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3779) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279208 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3781) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279209 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3790) (Stigmatellin Y) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 stigmatellin Y measurement http://www.ebi.ac.uk/efo/EFO_0803516 GCST90279210 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3794) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279211 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3796) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279212 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3798) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279213 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3815) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279214 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3829) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279215 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3842) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279216 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3844) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279217 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3847) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279218 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3850) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279219 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3860) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279220 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3863) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279221 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3864) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279222 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3867) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279223 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3870) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279224 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose levels 8,212 European ancestry individuals NA Affymetrix [15429302] (imputed) 1 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90200435 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenate levels 8,241 European ancestry individuals NA Affymetrix [15430311] (imputed) 3 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90200454 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Chiro-inositol levels 4,429 European ancestry individuals NA Affymetrix [15438875] (imputed) 0 chiro-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800270 GCST90199843 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) levels 8,266 European ancestry individuals NA Affymetrix [15431047] (imputed) 6 1-palmitoyl-2-linoleoyl-GPE (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800272 GCST90199844 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphinganine-1-phosphate levels 8,126 European ancestry individuals NA Affymetrix [15426841] (imputed) 1 sphinganine-1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800274 GCST90199845 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-stearoyl-sphingosine (d18:1/18:0) levels 8,233 European ancestry individuals NA Affymetrix [15430876] (imputed) 5 glycosyl-N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800275 GCST90199846 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylphenol sulfate levels 8,240 European ancestry individuals NA Affymetrix [15430706] (imputed) 1 4-allylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800958 GCST90199847 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinylcarnitine levels 8,212 European ancestry individuals NA Affymetrix [15429213] (imputed) 5 succinylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0020020 GCST90199848 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 21-hydroxypregnenolone disulfate levels 8,132 European ancestry individuals NA Affymetrix [15427123] (imputed) 5 21-hydroxypregnenolone disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800281 GCST90199849 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17alpha-diol monosulfate levels 5,524 European ancestry individuals NA Affymetrix [15287918] (imputed) 6 5alpha-androstan-3alpha,17alpha-diol monosulfate measurement http://www.ebi.ac.uk/efo/EFO_0800283 GCST90199850 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) disulfate (2) levels 8,205 European ancestry individuals NA Affymetrix [15429506] (imputed) 3 androstenediol (3beta,17beta) disulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800280 GCST90199851 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17alpha-diol disulfate levels 7,103 European ancestry individuals NA Affymetrix [15382959] (imputed) 3 5alpha-androstan-3beta,17alpha-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800289 GCST90199852 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20beta-diol monosulfate (1) levels 7,772 European ancestry individuals NA Affymetrix [15411349] (imputed) 4 5alpha-pregnan-3beta,20beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800284 GCST90199853 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) levels 8,028 European ancestry individuals NA Affymetrix [15421968] (imputed) 2 5alpha-pregnan-3beta,20alpha-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800285 GCST90199854 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17beta-diol monosulfate (2) levels 7,066 European ancestry individuals NA Affymetrix [15381870] (imputed) 3 5alpha-androstan-3beta,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800291 GCST90199855 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3alpha, 17alpha) monosulfate (3) levels 8,192 European ancestry individuals NA Affymetrix [15427785] (imputed) 6 androstenediol (3alpha, 17alpha) monosulfate (3) measurement http://www.ebi.ac.uk/efo/EFO_0800293 GCST90199856 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-diol disulfate levels 4,110 European ancestry individuals NA Affymetrix [15414471] (imputed) 2 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90199857 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (1) levels 7,608 European ancestry individuals NA Affymetrix [15403280] (imputed) 7 5alpha-androstan-3alpha,17beta-diol monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800288 GCST90199858 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol disulfate levels 5,082 European ancestry individuals NA Affymetrix [15262122] (imputed) 2 5alpha-androstan-3alpha,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800287 GCST90199859 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Andro steroid monosulfate C19H28O6S (1) levels 7,415 European ancestry individuals NA Affymetrix [15400078] (imputed) 4 andro steroid monosulfate C19H28O6S (1) measurement http://www.ebi.ac.uk/efo/EFO_0800305 GCST90199860 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol sulfate (C21H34O5S) levels 8,260 European ancestry individuals NA Affymetrix [15431064] (imputed) 3 pregnenediol sulfate (C21H34O5S) measurement http://www.ebi.ac.uk/efo/EFO_0800299 GCST90199861 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxycoumarin levels 6,944 European ancestry individuals NA Affymetrix [15374017] (imputed) 0 4-hydroxycoumarin measurement http://www.ebi.ac.uk/efo/EFO_0800959 GCST90199862 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 16a-hydroxy DHEA 3-sulfate levels 8,236 European ancestry individuals NA Affymetrix [15430452] (imputed) 3 16a-hydroxy DHEA 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800301 GCST90199863 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC levels 8,258 European ancestry individuals NA Affymetrix [15431258] (imputed) 1 gamma-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800160 GCST90199864 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyglutarate levels 7,769 European ancestry individuals NA Affymetrix [15410641] (imputed) 2 2-hydroxyglutarate measurement http://www.ebi.ac.uk/efo/EFO_0021506 GCST90199865 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-beta-alanine levels 8,231 European ancestry individuals NA Affymetrix [15429802] (imputed) 3 N-acetyl-beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0021430 GCST90199866 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tridecenedioate (C13:1-DC) levels 8,231 European ancestry individuals NA Affymetrix [15430032] (imputed) 1 tridecenedioate (C13:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800309 GCST90199867 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-3-methylhistidine levels 7,018 European ancestry individuals NA Affymetrix [15375592] (imputed) 1 N-acetyl-3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800044 GCST90199868 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyhippurate levels 8,241 European ancestry individuals NA Affymetrix [15430548] (imputed) 0 3-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0800960 GCST90199869 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-cholesten-3-one levels 6,990 European ancestry individuals NA Affymetrix [15371286] (imputed) 1 4-cholesten-3-one measurement http://www.ebi.ac.uk/efo/EFO_0800310 GCST90199870 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) monosulfate (2) levels 7,811 European ancestry individuals NA Affymetrix [15413054] (imputed) 3 androstenediol (3beta,17beta) monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800295 GCST90199871 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) monosulfate (1) levels 8,229 European ancestry individuals NA Affymetrix [15430268] (imputed) 1 androstenediol (3beta,17beta) monosulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800294 GCST90199872 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenolone sulfate levels 7,772 European ancestry individuals NA Affymetrix [15413931] (imputed) 2 pregnenolone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800303 GCST90199873 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylmethionine levels 6,674 European ancestry individuals NA Affymetrix [15364965] (imputed) 0 S-methylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800042 GCST90199874 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 13-HODE + 9-HODE levels 8,207 European ancestry individuals NA Affymetrix [15428910] (imputed) 0 13-HODE + 9-HODE measurement http://www.ebi.ac.uk/efo/EFO_0800308 GCST90199875 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl sphingomyelin (d18:1/16:0) levels 8,269 European ancestry individuals NA Affymetrix [15431031] (imputed) 0 palmitoyl sphingomyelin (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800300 GCST90199876 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indole-3-carboxylate levels 4,989 European ancestry individuals NA Affymetrix [15470849] (imputed) 1 indole-3-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800043 GCST90199877 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/18:1, d18:2/18:0) levels 8,267 European ancestry individuals NA Affymetrix [15431499] (imputed) 2 Sphingomyelin (d18:1/18:1, d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0022108 GCST90199878 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ergothioneine levels 8,210 European ancestry individuals NA Affymetrix [15429529] (imputed) 2 ergothioneine measurement http://www.ebi.ac.uk/efo/EFO_0021163 GCST90199879 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoylcarnitine (C10:1) levels 8,239 European ancestry individuals NA Affymetrix [15429223] (imputed) 4 cis-4-decenoylcarnitine (C10:1) measurement http://www.ebi.ac.uk/efo/EFO_0800311 GCST90199880 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-(galactosylhydroxy)-L-lysine levels 6,898 European ancestry individuals NA Affymetrix [15373827] (imputed) 0 5-(galactosylhydroxy)-L-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800048 GCST90199881 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2s,3R-dihydroxybutyrate levels 8,252 European ancestry individuals NA Affymetrix [15430874] (imputed) 1 2s,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800312 GCST90199882 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine disulfide levels 8,216 European ancestry individuals NA Affymetrix [15430163] (imputed) 4 cysteinylglycine disulfide measurement http://www.ebi.ac.uk/efo/EFO_0800049 GCST90199883 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxyisovalerate levels 8,268 European ancestry individuals NA Affymetrix [15431341] (imputed) 0 2,3-dihydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800963 GCST90199884 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutaramate levels 8,210 European ancestry individuals NA Affymetrix [15428556] (imputed) 1 alpha-ketoglutaramate measurement http://www.ebi.ac.uk/efo/EFO_0800046 GCST90199885 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutaconate levels 8,197 European ancestry individuals NA Affymetrix [15429664] (imputed) 4 3-methylglutaconate measurement http://www.ebi.ac.uk/efo/EFO_0800047 GCST90199886 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (16 or 17)-methylstearate (a19:0 or i19:0) levels 8,239 European ancestry individuals NA Affymetrix [15429669] (imputed) 0 (16 or 17)-methylstearate (a19:0 or i19:0) measurement http://www.ebi.ac.uk/efo/EFO_0800313 GCST90199887 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cinnamoylglycine levels 7,824 European ancestry individuals NA Affymetrix [15412918] (imputed) 1 cinnamoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800962 GCST90199888 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2R,3R-dihydroxybutyrate levels 8,223 European ancestry individuals NA Affymetrix [15428972] (imputed) 5 2R,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800314 GCST90199889 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyglutamate levels 7,226 European ancestry individuals NA Affymetrix [15386294] (imputed) 1 4-hydroxyglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800052 GCST90199890 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisone levels 8,153 European ancestry individuals NA Affymetrix [15427119] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90200360 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-alanine levels 8,114 European ancestry individuals NA Affymetrix [15426436] (imputed) 1 beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0800640 GCST90200361 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinate levels 7,943 European ancestry individuals NA Affymetrix [15419404] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90200362 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphocholine levels 8,245 European ancestry individuals NA Affymetrix [15429912] (imputed) 3 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90200363 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine levels 8,214 European ancestry individuals NA Affymetrix [15428968] (imputed) 3 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90200364 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylpyruvate levels 8,241 European ancestry individuals NA Affymetrix [15430365] (imputed) 2 phenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800132 GCST90200365 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatinine levels 8,239 European ancestry individuals NA Affymetrix [15430217] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90200366 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-Hydroxybutyrate levels 8,292 European ancestry individuals NA Affymetrix [15432082] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90200367 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol levels 8,258 European ancestry individuals NA Affymetrix [15431237] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90200368 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyphenylacetate levels 7,564 European ancestry individuals NA Affymetrix [15404594] (imputed) 2 2-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800131 GCST90200369 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate levels 8,253 European ancestry individuals NA Affymetrix [15430779] (imputed) 1 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90200370 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(4-hydroxyphenyl)lactate levels 8,259 European ancestry individuals NA Affymetrix [15430789] (imputed) 1 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90200371 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine levels 8,237 European ancestry individuals NA Affymetrix [15429048] (imputed) 4 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90200372 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gluconate levels 8,106 European ancestry individuals NA Affymetrix [15424939] (imputed) 1 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90200373 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphinganine levels 7,429 European ancestry individuals NA Affymetrix [15395846] (imputed) 1 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90200374 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamate levels 8,244 European ancestry individuals NA Affymetrix [15430139] (imputed) 2 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90200375 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Flavin adenine dinucleotide (FAD) levels 6,257 European ancestry individuals NA Affymetrix [15337653] (imputed) 2 flavin adenine dinucleotide (FAD) measurement http://www.ebi.ac.uk/efo/EFO_0800177 GCST90200376 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine levels 8,223 European ancestry individuals NA Affymetrix [15430081] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90200377 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisol levels (plasma) 8,193 European ancestry individuals NA Affymetrix [15428166] (imputed) 1 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90200378 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hypotaurine levels 8,212 European ancestry individuals NA Affymetrix [15430104] (imputed) 2 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90200379 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarate (C5-DC) levels 7,757 European ancestry individuals NA Affymetrix [15413654] (imputed) 0 glutarate (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800620 GCST90200380 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-1-pyrroline-5-carboxylate levels 8,232 European ancestry individuals NA Affymetrix [15430403] (imputed) 2 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90200381 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystine levels 8,177 European ancestry individuals NA Affymetrix [15426754] (imputed) 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90200382 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystathionine levels 8,014 European ancestry individuals NA Affymetrix [15422060] (imputed) 1 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90200383 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guanidinoacetate levels 8,238 European ancestry individuals NA Affymetrix [15430738] (imputed) 4 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90200384 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine levels 8,239 European ancestry individuals NA Affymetrix [15430622] (imputed) 1 S-methylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800054 GCST90199891 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoursodeoxycholate levels 8,234 European ancestry individuals NA Affymetrix [15429765] (imputed) 0 isoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800315 GCST90199892 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoate (10:1n6) levels 8,173 European ancestry individuals NA Affymetrix [15425854] (imputed) 2 cis-4-decenoate (10:1n6) measurement http://www.ebi.ac.uk/efo/EFO_0800318 GCST90199893 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-oxo-retinoic acid levels 7,514 European ancestry individuals NA Affymetrix [15398514] (imputed) 2 blood 4-oxo-retinoic acid measurement http://www.ebi.ac.uk/efo/EFO_0022216 GCST90199894 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-lignoceroyl-GPC (24:0) levels 8,208 European ancestry individuals NA Affymetrix [15429351] (imputed) 1 1-lignoceroyl-GPC (24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800322 GCST90199895 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate levels 8,230 European ancestry individuals NA Affymetrix [15430459] (imputed) 0 sulfate measurement http://www.ebi.ac.uk/efo/EFO_0007864 GCST90199896 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxy-2-oxoglutaric acid levels 7,919 European ancestry individuals NA Affymetrix [15419695] (imputed) 0 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90199897 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholate levels 8,252 European ancestry individuals NA Affymetrix [15431087] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90199898 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPC (p-16:0) levels 8,170 European ancestry individuals NA Affymetrix [15428441] (imputed) 3 1-(1-enyl-palmitoyl)-GPC (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800323 GCST90199899 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Argininate levels 8,226 European ancestry individuals NA Affymetrix [15429013] (imputed) 5 argininate measurement http://www.ebi.ac.uk/efo/EFO_0800055 GCST90199900 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-5-imidazoleacetate levels 8,171 European ancestry individuals NA Affymetrix [15427541] (imputed) 1 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90199901 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydantoin-5-propionate levels 8,164 European ancestry individuals NA Affymetrix [15427189] (imputed) 2 hydantoin-5-propionate measurement http://www.ebi.ac.uk/efo/EFO_0800051 GCST90199902 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-oxoarginine levels 8,223 European ancestry individuals NA Affymetrix [15429542] (imputed) 1 2-oxoarginine measurement http://www.ebi.ac.uk/efo/EFO_0800056 GCST90199903 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantoate levels 7,662 European ancestry individuals NA Affymetrix [15405454] (imputed) 0 blood pantoate measurement http://www.ebi.ac.uk/efo/EFO_0022210 GCST90199904 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Formiminoglutamate levels 8,175 European ancestry individuals NA Affymetrix [15429104] (imputed) 0 formiminoglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800050 GCST90199905 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPE (p-16:0) levels 8,227 European ancestry individuals NA Affymetrix [15429960] (imputed) 0 1-(1-enyl-palmitoyl)-GPE (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800334 GCST90199906 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine sulfoxide levels 8,255 European ancestry individuals NA Affymetrix [15431132] (imputed) 0 S-methylcysteine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0800058 GCST90199907 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-o-methylascorbic acid levels 8,219 European ancestry individuals NA Affymetrix [15429532] (imputed) 2 2-O-methylascorbic acid measurement http://www.ebi.ac.uk/efo/EFO_0800164 GCST90199908 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosanedioate (C20-DC) levels 8,258 European ancestry individuals NA Affymetrix [15431658] (imputed) 1 eicosanedioate (C20-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800330 GCST90199909 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-GPE (p-18:0) levels 8,249 European ancestry individuals NA Affymetrix [15430683] (imputed) 2 1-(1-enyl-stearoyl)-GPE (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800335 GCST90199910 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-citrylglutamate levels 8,226 European ancestry individuals NA Affymetrix [15428418] (imputed) 6 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90199911 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-oleoyltaurine levels 7,375 European ancestry individuals NA Affymetrix [15399662] (imputed) 2 N-oleoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800337 GCST90199912 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosadioate (C22-DC) levels 8,225 European ancestry individuals NA Affymetrix [15430526] (imputed) 0 docosadioate (C22-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800331 GCST90199913 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl-linoleoyl-glycerol (18:1/18:2) [2] levels 8,069 European ancestry individuals NA Affymetrix [15421754] (imputed) 4 oleoyl-linoleoyl-glycerol (18:1/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800333 GCST90199914 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole propionate levels 7,776 European ancestry individuals NA Affymetrix [15411851] (imputed) 1 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90199915 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C18:2 levels 8,268 European ancestry individuals NA Affymetrix [15431421] (imputed) 3 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90199916 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnanediol-3-glucuronide levels 7,905 European ancestry individuals NA Affymetrix [15417781] (imputed) 4 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90199917 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carboxyethyl-gaba levels 8,090 European ancestry individuals NA Affymetrix [15425127] (imputed) 2 carboxyethyl-GABA measurement http://www.ebi.ac.uk/efo/EFO_0800059 GCST90199918 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alliin levels 6,517 European ancestry individuals NA Affymetrix [15353233] (imputed) 1 alliin measurement http://www.ebi.ac.uk/efo/EFO_0800970 GCST90199919 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trimethylamine n-oxide levels 8,218 European ancestry individuals NA Affymetrix [15430398] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90199920 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulate levels 6,398 European ancestry individuals NA Affymetrix [15341969] (imputed) 0 dihydroferulate measurement http://www.ebi.ac.uk/efo/EFO_0800969 GCST90199921 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Prolylglycine levels 7,907 European ancestry individuals NA Affymetrix [15418917] (imputed) 1 prolylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800683 GCST90199922 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoylglycine levels 8,236 European ancestry individuals NA Affymetrix [15428633] (imputed) 2 N-palmitoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800342 GCST90199923 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyltaurine levels 5,440 European ancestry individuals NA Affymetrix [15275322] (imputed) 0 N-methyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800064 GCST90199924 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinimide levels 5,865 European ancestry individuals NA Affymetrix [15305762] (imputed) 1 blood succinimide measurement http://www.ebi.ac.uk/efo/EFO_0022211 GCST90199925 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcarnosine levels 8,233 European ancestry individuals NA Affymetrix [15430258] (imputed) 6 blood N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022217 GCST90199926 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine betaine (hercynine) levels 7,518 European ancestry individuals NA Affymetrix [15401295] (imputed) 2 histidine betaine (hercynine) measurement http://www.ebi.ac.uk/efo/EFO_0800972 GCST90199927 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-stearoyl-GPE (18:0) levels 8,073 European ancestry individuals NA Affymetrix [15425599] (imputed) 3 2-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800343 GCST90199928 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margaroylcarnitine (C17) levels 8,112 European ancestry individuals NA Affymetrix [15424671] (imputed) 2 margaroylcarnitine (C17) measurement http://www.ebi.ac.uk/efo/EFO_0800345 GCST90199929 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (R)-3-hydroxybutyrylcarnitine levels 7,787 European ancestry individuals NA Affymetrix [15412386] (imputed) 1 (R)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800344 GCST90199930 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lanthionine levels 7,760 European ancestry individuals NA Affymetrix [15411249] (imputed) 0 lanthionine measurement http://www.ebi.ac.uk/efo/EFO_0800063 GCST90199931 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannonate levels 8,166 European ancestry individuals NA Affymetrix [15426658] (imputed) 1 mannonate measurement http://www.ebi.ac.uk/efo/EFO_0800971 GCST90199932 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3b-hydroxy-5-cholenoic acid levels 6,846 European ancestry individuals NA Affymetrix [15371635] (imputed) 1 3b-hydroxy-5-cholenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800348 GCST90199933 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxydecanoate levels 8,267 European ancestry individuals NA Affymetrix [15431674] (imputed) 1 2-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800347 GCST90199934 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycohyocholate levels 7,095 European ancestry individuals NA Affymetrix [15388247] (imputed) 1 glycohyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800346 GCST90199935 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (2) levels 6,320 European ancestry individuals NA Affymetrix [15330990] (imputed) 0 3-methyl catechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800973 GCST90199936 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminooctanoate levels 8,178 European ancestry individuals NA Affymetrix [15428576] (imputed) 2 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90199937 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (1) levels 8,233 European ancestry individuals NA Affymetrix [15428063] (imputed) 0 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90199938 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylcatechol sulfate levels 8,229 European ancestry individuals NA Affymetrix [15429970] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90199939 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guaiacol sulfate levels 8,262 European ancestry individuals NA Affymetrix [15431355] (imputed) 0 guaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800978 GCST90199940 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC glucuronide levels 6,305 European ancestry individuals NA Affymetrix [15336085] (imputed) 1 gamma-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800165 GCST90199941 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethyl sulfone levels 7,905 European ancestry individuals NA Affymetrix [15417516] (imputed) 0 dimethyl sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800979 GCST90199942 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-piperidinone levels 8,225 European ancestry individuals NA Affymetrix [15429002] (imputed) 0 2-piperidinone measurement http://www.ebi.ac.uk/efo/EFO_0800980 GCST90199943 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolin-2-one levels 7,027 European ancestry individuals NA Affymetrix [15380453] (imputed) 1 indolin-2-one measurement http://www.ebi.ac.uk/efo/EFO_0800981 GCST90199944 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels 8,254 European ancestry individuals NA Affymetrix [15430478] (imputed) 2 Sphingomyelin (d18:1/14:0, d16:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022105 GCST90199945 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-acetylphenol sulfate levels 6,897 European ancestry individuals NA Affymetrix [15375123] (imputed) 0 3-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800983 GCST90199946 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels 8,272 European ancestry individuals NA Affymetrix [15431683] (imputed) 0 Sphingomyelin (d18:2/16:0, d18:1/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0022115 GCST90199947 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-allylcysteine levels 6,857 European ancestry individuals NA Affymetrix [15375281] (imputed) 1 S-allylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800985 GCST90199948 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-oxopiperidine-2-carboxylate levels 8,032 European ancestry individuals NA Affymetrix [15421411] (imputed) 2 6-oxopiperidine-2-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800066 GCST90199949 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminophenol sulfate levels 8,264 European ancestry individuals NA Affymetrix [15430816] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90199950 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylalliin levels 5,432 European ancestry individuals NA Affymetrix [15277052] (imputed) 1 N-acetylalliin measurement http://www.ebi.ac.uk/efo/EFO_0800987 GCST90199951 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeine levels 8,005 European ancestry individuals NA Affymetrix [15423165] (imputed) 0 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90200436 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructose levels 8,137 European ancestry individuals NA Affymetrix [15426981] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90200437 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate levels 8,192 European ancestry individuals NA Affymetrix [15428244] (imputed) 0 alpha-ketobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800140 GCST90200438 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine levels 8,216 European ancestry individuals NA Affymetrix [15429409] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90200439 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Blood sugar levels 8,123 European ancestry individuals NA Affymetrix [15426368] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90200440 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan levels 8,235 European ancestry individuals NA Affymetrix [15430212] (imputed) 2 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90200441 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Valine levels 8,247 European ancestry individuals NA Affymetrix [15430786] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90200442 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pseudouridine levels 8,213 European ancestry individuals NA Affymetrix [15429589] (imputed) 1 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90200443 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroorotate levels 8,195 European ancestry individuals NA Affymetrix [15426607] (imputed) 6 dihydroorotate measurement http://www.ebi.ac.uk/efo/EFO_0800647 GCST90200444 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caprylate (8:0) levels 8,163 European ancestry individuals NA Affymetrix [15425354] (imputed) 1 caprylate 8:0 measurement http://www.ebi.ac.uk/efo/EFO_0021103 GCST90200445 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidate (20:0) levels 8,228 European ancestry individuals NA Affymetrix [15430570] (imputed) 0 arachidate (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800625 GCST90200446 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maltose levels in coronary artery disease 6,351 European ancestry individuals NA Affymetrix [15347032] (imputed) 0 Maltose measurement http://www.ebi.ac.uk/efo/EFO_0021649 GCST90200447 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphinganine (d18:0/18:0) levels 6,737 European ancestry individuals NA Affymetrix [15367087] (imputed) 1 N-stearoyl-sphinganine (d18:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800626 GCST90200448 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sucrose levels 7,803 European ancestry individuals NA Affymetrix [15415171] (imputed) 0 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90200449 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phytanate levels 8,223 European ancestry individuals NA Affymetrix [15429970] (imputed) 0 phytanate measurement http://www.ebi.ac.uk/efo/EFO_0801065 GCST90200410 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free proline levels 8,257 European ancestry individuals NA Affymetrix [15431336] (imputed) 3 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90200411 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate levels 8,287 European ancestry individuals NA Affymetrix [15432170] (imputed) 1 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90200412 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-deoxyuridine levels 7,915 European ancestry individuals NA Affymetrix [15415683] (imputed) 3 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90200413 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristate (14:0) levels 8,282 European ancestry individuals NA Affymetrix [15431724] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90200414 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine levels 8,271 European ancestry individuals NA Affymetrix [15431627] (imputed) 3 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90200415 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-urocanate levels 8,198 European ancestry individuals NA Affymetrix [15429044] (imputed) 1 trans-urocanate measurement http://www.ebi.ac.uk/efo/EFO_0800138 GCST90200416 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urea levels 8,238 European ancestry individuals NA Affymetrix [15430589] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90200417 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyridoxal levels 8,021 European ancestry individuals NA Affymetrix [15424075] (imputed) 0 blood pyridoxal measurement http://www.ebi.ac.uk/efo/EFO_0022222 GCST90200418 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine levels 8,253 European ancestry individuals NA Affymetrix [15430860] (imputed) 2 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90200419 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurine levels 8,219 European ancestry individuals NA Affymetrix [15430430] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90200420 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate levels 8,191 European ancestry individuals NA Affymetrix [15429328] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90200421 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serotonin levels 7,498 European ancestry individuals NA Affymetrix [15399118] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90200422 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine levels 7,348 European ancestry individuals NA Affymetrix [15391096] (imputed) 1 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90200423 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethylglycine levels 8,224 European ancestry individuals NA Affymetrix [15430076] (imputed) 5 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90200424 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Betaine levels 8,232 European ancestry individuals NA Affymetrix [15429964] (imputed) 6 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90200425 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xylose levels 6,822 European ancestry individuals NA Affymetrix [15364312] (imputed) 0 xylose measurement http://www.ebi.ac.uk/efo/EFO_0800153 GCST90200426 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyrosine levels 8,252 European ancestry individuals NA Affymetrix [15431184] (imputed) 2 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90200427 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caprate (10:0) levels 8,272 European ancestry individuals NA Affymetrix [15431487] (imputed) 0 caprate 10:0 measurement http://www.ebi.ac.uk/efo/EFO_0021101 GCST90200428 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytidine levels 7,659 European ancestry individuals NA Affymetrix [15408137] (imputed) 1 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90200429 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyruvate levels 8,259 European ancestry individuals NA Affymetrix [15431265] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90200430 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alanine levels 8,265 European ancestry individuals NA Affymetrix [15430972] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90200431 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonine levels 8,245 European ancestry individuals NA Affymetrix [15430264] (imputed) 3 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90200432 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytosine levels 6,990 European ancestry individuals NA Affymetrix [15376531] (imputed) 0 blood cytosine measurement http://www.ebi.ac.uk/efo/EFO_0022213 GCST90200433 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 12,13-DiHOME levels 7,918 European ancestry individuals NA Affymetrix [15419527] (imputed) 0 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90200434 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine levels 7,982 European ancestry individuals NA Affymetrix [15419250] (imputed) 1 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90200385 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholate levels 7,649 European ancestry individuals NA Affymetrix [15409155] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90200386 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholate levels 8,247 European ancestry individuals NA Affymetrix [15429694] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90200387 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoleate (16:1n7) levels 8,290 European ancestry individuals NA Affymetrix [15431891] (imputed) 1 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90200388 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Leucine levels 8,252 European ancestry individuals NA Affymetrix [15431186] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90200389 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearate (18:0) levels 8,272 European ancestry individuals NA Affymetrix [15431434] (imputed) 0 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90200390 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine levels 8,222 European ancestry individuals NA Affymetrix [15429509] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90200391 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotate levels 8,128 European ancestry individuals NA Affymetrix [15426966] (imputed) 2 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90200392 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate levels (UKB data field 30810) 8,247 European ancestry individuals NA Affymetrix [15430914] (imputed) 2 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90200393 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine levels 4,940 European ancestry individuals NA Affymetrix [15463011] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90200394 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine 5'-monophosphate (IMP) levels 4,639 European ancestry individuals NA Affymetrix [15456842] (imputed) 0 inosine 5'-monophosphate (IMP) measurement http://www.ebi.ac.uk/efo/EFO_0800641 GCST90200395 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylalanine levels 8,228 European ancestry individuals NA Affymetrix [15430190] (imputed) 1 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90200396 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitate (16:0) levels 8,269 European ancestry individuals NA Affymetrix [15431567] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90200397 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Malate levels 8,187 European ancestry individuals NA Affymetrix [15429235] (imputed) 2 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90200398 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoleucine levels 8,255 European ancestry individuals NA Affymetrix [15431154] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90200399 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nicotinamide levels 8,110 European ancestry individuals NA Affymetrix [15426273] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90200400 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myo-inositol levels 8,193 European ancestry individuals NA Affymetrix [15429363] (imputed) 1 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90200401 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lysine levels 8,250 European ancestry individuals NA Affymetrix [15430464] (imputed) 4 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90200402 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrulline levels 8,157 European ancestry individuals NA Affymetrix [15428505] (imputed) 2 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90200403 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ornithine levels 8,255 European ancestry individuals NA Affymetrix [15430703] (imputed) 1 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90200404 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Retinol (Vitamin A) levels 8,247 European ancestry individuals NA Affymetrix [15429676] (imputed) 1 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90200405 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylnicotinamide levels 8,194 European ancestry individuals NA Affymetrix [15429301] (imputed) 1 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90200406 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Uridine levels 8,253 European ancestry individuals NA Affymetrix [15430767] (imputed) 3 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90200407 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma lactate levels 8,217 European ancestry individuals NA Affymetrix [15429793] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90200408 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pristanate levels 6,497 European ancestry individuals NA Affymetrix [15349844] (imputed) 0 pristanate measurement http://www.ebi.ac.uk/efo/EFO_0800623 GCST90200409 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11843 levels 7,230 European ancestry individuals NA Affymetrix [15387369] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90200476 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12127 levels 5,878 European ancestry individuals NA Affymetrix [15310194] (imputed) 0 X-12127 measurement http://www.ebi.ac.uk/efo/EFO_0800709 GCST90200477 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12221 levels 6,819 European ancestry individuals NA Affymetrix [15363629] (imputed) 0 X-12221 measurement http://www.ebi.ac.uk/efo/EFO_0800711 GCST90200478 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12283 levels 7,763 European ancestry individuals NA Affymetrix [15406777] (imputed) 0 X-12283 measurement http://www.ebi.ac.uk/efo/EFO_0800713 GCST90200479 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12410 levels 7,442 European ancestry individuals NA Affymetrix [15398811] (imputed) 1 X-12410 measurement http://www.ebi.ac.uk/efo/EFO_0800715 GCST90200480 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12104 levels 7,194 European ancestry individuals NA Affymetrix [15387507] (imputed) 0 X-12104 measurement http://www.ebi.ac.uk/efo/EFO_0800703 GCST90200481 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12193 levels 7,705 European ancestry individuals NA Affymetrix [15406696] (imputed) 0 X-12193 measurement http://www.ebi.ac.uk/efo/EFO_0800710 GCST90200482 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12216 levels 8,181 European ancestry individuals NA Affymetrix [15428575] (imputed) 2 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90200483 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12306 levels 6,054 European ancestry individuals NA Affymetrix [15330050] (imputed) 0 X-12306 measurement http://www.ebi.ac.uk/efo/EFO_0800714 GCST90200484 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12100 levels 8,210 European ancestry individuals NA Affymetrix [15430162] (imputed) 3 X-12100 measurement http://www.ebi.ac.uk/efo/EFO_0800701 GCST90200485 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12261 levels 4,347 European ancestry individuals NA Affymetrix [15426492] (imputed) 0 X-12261 measurement http://www.ebi.ac.uk/efo/EFO_0021301 GCST90200486 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11880 levels 8,206 European ancestry individuals NA Affymetrix [15428916] (imputed) 3 X-11880 measurement http://www.ebi.ac.uk/efo/EFO_0800698 GCST90200487 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12117 levels 7,379 European ancestry individuals NA Affymetrix [15393585] (imputed) 4 X-12117 measurement http://www.ebi.ac.uk/efo/EFO_0800706 GCST90200488 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12407 levels 6,534 European ancestry individuals NA Affymetrix [15348660] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90200489 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12101 levels 8,217 European ancestry individuals NA Affymetrix [15430268] (imputed) 1 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90200490 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12026 levels 8,180 European ancestry individuals NA Affymetrix [15429366] (imputed) 0 X-12026 measurement http://www.ebi.ac.uk/efo/EFO_0800700 GCST90200491 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12411 levels 8,174 European ancestry individuals NA Affymetrix [15428714] (imputed) 3 X-12411 measurement http://www.ebi.ac.uk/efo/EFO_0800716 GCST90200492 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12013 levels 5,848 European ancestry individuals NA Affymetrix [15312597] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90200493 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12007 levels 8,002 European ancestry individuals NA Affymetrix [15421330] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90200494 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12462 levels 8,236 European ancestry individuals NA Affymetrix [15429928] (imputed) 0 X-12462 measurement http://www.ebi.ac.uk/efo/EFO_0800717 GCST90200495 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12714 levels 6,870 European ancestry individuals NA Affymetrix [15372741] (imputed) 1 X-12714 measurement http://www.ebi.ac.uk/efo/EFO_0800722 GCST90200496 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12740 levels 6,449 European ancestry individuals NA Affymetrix [15346050] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90200497 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12730 levels 7,133 European ancestry individuals NA Affymetrix [15384612] (imputed) 0 X-12730 measurement http://www.ebi.ac.uk/efo/EFO_0800724 GCST90200498 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12701 levels 6,278 European ancestry individuals NA Affymetrix [15330063] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200499 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12816 levels 5,190 European ancestry individuals NA Affymetrix [15259127] (imputed) 0 X-12816 measurement http://www.ebi.ac.uk/efo/EFO_0021336 GCST90200500 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800449 GCST90202520 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800464 GCST90202521 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcholine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 palmitoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800473 GCST90202522 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamate levels 58 East Asian ancestry individuals NA Affymetrix [4190023] (imputed) 0 phenylacetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800687 GCST90202523 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPG (18:2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-linoleoyl-GPG (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800472 GCST90202524 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (p-18:0/18:2) levels 103 East Asian ancestry individuals NA Affymetrix [4303764] (imputed) 0 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90202525 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Furaneol sulfate levels 89 East Asian ancestry individuals NA Affymetrix [4190608] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202526 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) levels 95 East Asian ancestry individuals NA Affymetrix [4273395] (imputed) 0 pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800494 GCST90202527 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 2-sulfate levels 99 East Asian ancestry individuals NA Affymetrix [4192689] (imputed) 0 ascorbic acid 2-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800169 GCST90202528 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800476 GCST90202529 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate glucuronide (1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90202530 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-3-hydroxybutyrylcarnitine levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 (S)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800475 GCST90202531 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methylcytidine levels 102 East Asian ancestry individuals NA Affymetrix [4317296] (imputed) 0 2'-O-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800635 GCST90202532 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinoylcarnitine levels 100 East Asian ancestry individuals NA Affymetrix [4353209] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202533 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methyluridine levels 94 East Asian ancestry individuals NA Affymetrix [4283091] (imputed) 0 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90202534 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonoylcholine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 arachidonoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800478 GCST90202535 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoylcholine levels 101 East Asian ancestry individuals NA Affymetrix [4336641] (imputed) 0 docosahexaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800479 GCST90202536 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenoyl-choline levels 84 East Asian ancestry individuals NA Affymetrix [4282454] (imputed) 0 dihomo-linolenoyl-choline measurement http://www.ebi.ac.uk/efo/EFO_0800481 GCST90202537 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeic acid sulfate levels 97 East Asian ancestry individuals NA Affymetrix [4237162] (imputed) 0 caffeic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801013 GCST90202538 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-2-methylbutyrate levels 98 East Asian ancestry individuals NA Affymetrix [4208855] (imputed) 0 blood 2,3-dihydroxy-2-methylbutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022219 GCST90202539 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetylglutamine levels 92 East Asian ancestry individuals NA Affymetrix [4327734] (imputed) 0 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90202540 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecadienoate (16:2n6) levels 103 East Asian ancestry individuals NA Affymetrix [4301369] (imputed) 0 hexadecadienoate (16:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800491 GCST90202541 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoleoylcarnitine (C16:1) levels 103 East Asian ancestry individuals NA Affymetrix [4302395] (imputed) 0 palmitoleoylcarnitine (C16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800493 GCST90202542 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) levels 103 East Asian ancestry individuals NA Affymetrix [4303956] (imputed) 0 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800483 GCST90202543 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcholine levels 102 East Asian ancestry individuals NA Affymetrix [4320879] (imputed) 0 oleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800477 GCST90202544 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (N(1) + N(8))-acetylspermidine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 blood N(1)-acetylspermidine measurement, blood N(8)-acetylspermidine measurement http://www.ebi.ac.uk/efo/EFO_0022204, http://www.ebi.ac.uk/efo/EFO_0022205 GCST90202595 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) levels 103 East Asian ancestry individuals NA Affymetrix [4298665] (imputed) 0 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) measurement http://www.ebi.ac.uk/efo/EFO_0800566 GCST90202596 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecadienedioate (C18:2-DC) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 octadecadienedioate (C18:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800565 GCST90202597 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyarachidate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-hydroxyarachidate measurement http://www.ebi.ac.uk/efo/EFO_0800558 GCST90202598 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortolone glucuronide (1) levels 102 East Asian ancestry individuals NA Affymetrix [4318346] (imputed) 0 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90202599 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C10H18O2 (7) levels 71 East Asian ancestry individuals NA Affymetrix [4358078] (imputed) 0 glucuronide of C10H18O2 (7) measurement http://www.ebi.ac.uk/efo/EFO_0800652 GCST90202600 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecenedioate (C12:1-DC) levels 103 East Asian ancestry individuals NA Affymetrix [4302331] (imputed) 0 dodecenedioate (C12:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800561 GCST90202601 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (3) levels 94 East Asian ancestry individuals NA Affymetrix [4283861] (imputed) 0 carotene diol (3) measurement http://www.ebi.ac.uk/efo/EFO_0800172 GCST90202602 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminooctanoate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90202603 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecenedioate (C16:1-DC) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90202604 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoleoylcarnitine levels 95 East Asian ancestry individuals NA Affymetrix [4270364] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202605 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Heptenedioate (C7:1-DC) levels 101 East Asian ancestry individuals NA Affymetrix [4335775] (imputed) 0 heptenedioate (C7:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800564 GCST90202606 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioate (C18:1-DC) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 octadecenedioate (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800563 GCST90202607 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-dodecenoylcarnitine (C12:1) levels 99 East Asian ancestry individuals NA Affymetrix [4192299] (imputed) 0 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90202608 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulic acid sulfate levels 68 East Asian ancestry individuals NA Affymetrix [4194016] (imputed) 0 dihydroferulic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801026 GCST90202609 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-amino-2-piperidone levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-amino-2-piperidone measurement http://www.ebi.ac.uk/efo/EFO_0800097 GCST90202610 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylhydroxyproline levels 89 East Asian ancestry individuals NA Affymetrix [4177932] (imputed) 0 N-methylhydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800093 GCST90202611 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glyco-beta-muricholate levels 88 East Asian ancestry individuals NA Affymetrix [4214941] (imputed) 0 glyco-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800569 GCST90202612 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,n,n-trimethyl-alanylproline betaine (tmap) levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 N,N,N-trimethyl-alanylproline betaine (TMAP) measurement http://www.ebi.ac.uk/efo/EFO_0800094 GCST90202613 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H12O2 levels 78 East Asian ancestry individuals NA Affymetrix [4188030] (imputed) 0 glycine conjugate of C10H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800654 GCST90202614 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanoate (PFOA) levels 102 East Asian ancestry individuals NA Affymetrix [4317378] (imputed) 0 perfluorooctanoate (PFOA) measurement http://www.ebi.ac.uk/efo/EFO_0801024 GCST90202615 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-formylindole levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-formylindole measurement http://www.ebi.ac.uk/efo/EFO_0801025 GCST90202616 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxyasparagine levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 hydroxyasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800092 GCST90202617 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylcitrulline levels 102 East Asian ancestry individuals NA Affymetrix [4318563] (imputed) 0 gamma-glutamylcitrulline measurement http://www.ebi.ac.uk/efo/EFO_0800690 GCST90202618 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 8-methoxykynurenate levels 84 East Asian ancestry individuals NA Affymetrix [4288166] (imputed) 0 8-methoxykynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800096 GCST90202619 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 pregnenetriol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800586 GCST90202670 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxy-4-(methylthio)butanoic acid levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-hydroxy-4-(methylthio)butanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800113 GCST90202671 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenedioate (C20:1-DC) levels 100 East Asian ancestry individuals NA Affymetrix [4350797] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202672 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-methylpyridine sulfate levels 88 East Asian ancestry individuals NA Affymetrix [4217222] (imputed) 0 3-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801052 GCST90202673 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholic acid 3-sulfate levels 94 East Asian ancestry individuals NA Affymetrix [4286840] (imputed) 0 taurochenodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800584 GCST90202674 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) levels 103 East Asian ancestry individuals NA Affymetrix [4299863] (imputed) 0 hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800583 GCST90202675 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Levulinoylcarnitine levels 87 East Asian ancestry individuals NA Affymetrix [4248272] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202676 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,5-dichloro-2,6-dihydroxybenzoic acid levels 102 East Asian ancestry individuals NA Affymetrix [4316363] (imputed) 0 3,5-dichloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801054 GCST90202677 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinoylglycine levels 96 East Asian ancestry individuals NA Affymetrix [4247567] (imputed) 0 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90202678 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Undecenoylcarnitine (C11:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90202679 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoylcarnitine levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 3-hydroxydecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800590 GCST90202680 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched chain 14:0 dicarboxylic acid levels 94 East Asian ancestry individuals NA Affymetrix [4287330] (imputed) 0 branched chain 14:0 dicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0800593 GCST90202681 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxy-N6,N6,N6-trimethyllysine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 hydroxy-N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800112 GCST90202682 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800591 GCST90202683 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic acid glycine levels 92 East Asian ancestry individuals NA Affymetrix [4327528] (imputed) 0 vanillic acid glycine measurement http://www.ebi.ac.uk/efo/EFO_0801056 GCST90202684 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinoyltaurine levels 97 East Asian ancestry individuals NA Affymetrix [4232104] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202685 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-a-amino-omega-caprolactam levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 (S)-a-amino-omega-caprolactam measurement http://www.ebi.ac.uk/efo/EFO_0801055 GCST90202686 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Metabolonic lactone sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90202687 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienedioate (C14:2-DC) levels 92 East Asian ancestry individuals NA Affymetrix [4329130] (imputed) 0 tetradecadienedioate (C14:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800585 GCST90202688 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dibutyl sulfosuccinate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 blood dibutyl sulfosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0022212 GCST90202689 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) measurement http://www.ebi.ac.uk/efo/EFO_0800661 GCST90202690 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-bromo-5-chloro-2,6-dihydroxybenzoic acid levels 101 East Asian ancestry individuals NA Affymetrix [4334700] (imputed) 0 3-bromo-5-chloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801058 GCST90202691 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentose acid levels 103 East Asian ancestry individuals NA Affymetrix [4303044] (imputed) 0 pentose acid measurement http://www.ebi.ac.uk/efo/EFO_0800660 GCST90202692 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-carboxyethylcysteine levels 98 East Asian ancestry individuals NA Affymetrix [4216870] (imputed) 0 L-Cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021614 GCST90202693 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylcarnitine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202694 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecadienoate (12:2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 dodecadienoate (12:2) measurement http://www.ebi.ac.uk/efo/EFO_0800572 GCST90202645 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-isoputreanine levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 N-acetyl-isoputreanine measurement http://www.ebi.ac.uk/efo/EFO_0800107 GCST90202646 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl leucine levels 99 East Asian ancestry individuals NA Affymetrix [4200728] (imputed) 0 N-acetyl-l-leucine measurement http://www.ebi.ac.uk/efo/EFO_0021653 GCST90202647 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 3-sulfate levels 102 East Asian ancestry individuals NA Affymetrix [4319104] (imputed) 0 ascorbic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800173 GCST90202648 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyetiocholanolone glucuronide levels 69 East Asian ancestry individuals NA Affymetrix [4168019] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202649 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ethylcatechol sulfate (1) levels 78 East Asian ancestry individuals NA Affymetrix [4220688] (imputed) 0 3-ethylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801047 GCST90202650 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6-methyllysine levels 96 East Asian ancestry individuals NA Affymetrix [4248210] (imputed) 0 N2-acetyl,N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800109 GCST90202651 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6,N6-dimethyllysine levels 89 East Asian ancestry individuals NA Affymetrix [4170958] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202652 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (3) levels 87 East Asian ancestry individuals NA Affymetrix [4234040] (imputed) 0 sulfate of piperine metabolite C18H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801037 GCST90202653 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylcatechol sulfate levels 99 East Asian ancestry individuals NA Affymetrix [4200525] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90202654 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylcatechol sulfate (1) levels 88 East Asian ancestry individuals NA Affymetrix [4214662] (imputed) 0 4-acetylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801049 GCST90202655 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid glucuronide levels 87 East Asian ancestry individuals NA Affymetrix [4226109] (imputed) 0 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90202656 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyandrosterone glucuronide levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90202657 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylhexanoylglutamine levels 59 East Asian ancestry individuals NA Affymetrix [4152480] (imputed) 0 4-methylhexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800576 GCST90202658 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxy-2-methylpyridine sulfate levels 79 East Asian ancestry individuals NA Affymetrix [4184407] (imputed) 0 5-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801051 GCST90202659 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylcatechol sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4302736] (imputed) 0 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90202660 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-ketocaprylate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-ketocaprylate measurement http://www.ebi.ac.uk/efo/EFO_0800110 GCST90202661 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoylcarnitine (1) levels 103 East Asian ancestry individuals NA Affymetrix [4301041] (imputed) 0 3-hydroxyhexanoylcarnitine (1) measurement http://www.ebi.ac.uk/efo/EFO_0800580 GCST90202662 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,6-dihydroxybenzoic acid levels 103 East Asian ancestry individuals NA Affymetrix [4302350] (imputed) 0 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90202663 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lithocholate sulfate (1) levels 85 East Asian ancestry individuals NA Affymetrix [4272389] (imputed) 0 lithocholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800579 GCST90202664 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydrocaffeate sulfate (2) levels 83 East Asian ancestry individuals NA Affymetrix [4313651] (imputed) 0 dihydrocaffeate sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801044 GCST90202665 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl vanillate sulfate levels 63 East Asian ancestry individuals NA Affymetrix [4324612] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202666 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholic acid sulfate (1) levels 100 East Asian ancestry individuals NA Affymetrix [4347924] (imputed) 0 glycoursodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800578 GCST90202667 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-5-methylthio-4-pentenoate (dmtpa) levels 102 East Asian ancestry individuals NA Affymetrix [4317062] (imputed) 0 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90202668 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol disulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90202669 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N,N-trimethyl-5-aminovalerate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90202570 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/23:1) levels 103 East Asian ancestry individuals NA Affymetrix [4299732] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202571 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0) levels 102 East Asian ancestry individuals NA Affymetrix [4316221] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202572 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:2/16:0, d18:2/15:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202573 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Heneicosapentaenoate (21:5n3) levels 87 East Asian ancestry individuals NA Affymetrix [4233547] (imputed) 0 heneicosapentaenoate (21:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800537 GCST90202574 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoylcarnitine (C22) levels 99 East Asian ancestry individuals NA Affymetrix [4195175] (imputed) 0 behenoylcarnitine (C22) measurement http://www.ebi.ac.uk/efo/EFO_0800539 GCST90202575 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cerotoylcarnitine (C26) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 cerotoylcarnitine (C26) measurement http://www.ebi.ac.uk/efo/EFO_0800542 GCST90202576 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonoylcarnitine (C20:4) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 arachidonoylcarnitine (C20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800544 GCST90202577 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroylcarnitine (C24) levels 103 East Asian ancestry individuals NA Affymetrix [4299732] (imputed) 0 lignoceroylcarnitine (C24) measurement http://www.ebi.ac.uk/efo/EFO_0800541 GCST90202578 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoylcarnitine (C20:1) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 eicosenoylcarnitine (C20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800545 GCST90202579 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidoylcarnitine (C20) levels 103 East Asian ancestry individuals NA Affymetrix [4303061] (imputed) 0 arachidoylcarnitine (C20) measurement http://www.ebi.ac.uk/efo/EFO_0800540 GCST90202580 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenoylcarnitine (C20:3n3 or 6) levels 102 East Asian ancestry individuals NA Affymetrix [4316751] (imputed) 0 dihomo-linolenoylcarnitine (C20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800547 GCST90202581 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nervonoylcarnitine (C24:1) levels 101 East Asian ancestry individuals NA Affymetrix [4335714] (imputed) 0 nervonoylcarnitine (C24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800549 GCST90202582 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:1/20:0, d16:1/22:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycosyl ceramide (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800551 GCST90202583 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 carotene diol (2) measurement http://www.ebi.ac.uk/efo/EFO_0800171 GCST90202584 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethyl alpha-glucopyranoside levels 74 East Asian ancestry individuals NA Affymetrix [4254186] (imputed) 0 ethyl alpha-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801019 GCST90202585 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (1) levels 103 East Asian ancestry individuals NA Affymetrix [4300485] (imputed) 0 carotene diol (1) measurement http://www.ebi.ac.uk/efo/EFO_0800170 GCST90202586 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenoylcarnitine (C18:3) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 linolenoylcarnitine (C18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800538 GCST90202587 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoylcarnitine (C22:6) levels 92 East Asian ancestry individuals NA Affymetrix [4334091] (imputed) 0 docosahexaenoylcarnitine (C22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800548 GCST90202588 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-furoylcarnitine levels 67 East Asian ancestry individuals NA Affymetrix [4202431] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202589 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-butenoylglycine levels 65 East Asian ancestry individuals NA Affymetrix [4244332] (imputed) 0 2-butenoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800556 GCST90202590 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C12H22O4 (1) levels 70 East Asian ancestry individuals NA Affymetrix [4379752] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202591 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxy-cmpf levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 hydroxy-CMPF measurement http://www.ebi.ac.uk/efo/EFO_0800557 GCST90202592 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-2-hexenoylglycine levels 74 East Asian ancestry individuals NA Affymetrix [4304843] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202593 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyphenylacetoylglutamine levels 54 East Asian ancestry individuals NA Affymetrix [4278244] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202594 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C7H12O2 levels 91 East Asian ancestry individuals NA Affymetrix [4346235] (imputed) 0 glutamine conjugate of C7H12O2 measurement http://www.ebi.ac.uk/efo/EFO_0800656 GCST90202620 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxybutyroylglycine levels 99 East Asian ancestry individuals NA Affymetrix [4192457] (imputed) 0 3-hydroxybutyroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800568 GCST90202621 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N-dimethylalanine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N,N-dimethylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800098 GCST90202622 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienoate (14:2) levels 103 East Asian ancestry individuals NA Affymetrix [4302395] (imputed) 0 tetradecadienoate (14:2) measurement http://www.ebi.ac.uk/efo/EFO_0800570 GCST90202623 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine conjugate of C10H14O2 (1) levels 103 East Asian ancestry individuals NA Affymetrix [4301860] (imputed) 0 glycine conjugate of C10H14O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800655 GCST90202624 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoleglyoxylic acid levels 100 East Asian ancestry individuals NA Affymetrix [4351564] (imputed) 0 3-indoleglyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801027 GCST90202625 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (1) levels 91 East Asian ancestry individuals NA Affymetrix [4337864] (imputed) 0 glutamine conjugate of C6H10O2 (1) measurement http://www.ebi.ac.uk/efo/EFO_0800657 GCST90202626 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/14:0, d16:1/15:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202627 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine conjugate of C6H10O2 (2) levels 103 East Asian ancestry individuals NA Affymetrix [4300825] (imputed) 0 glutamine conjugate of C6H10O2 (2) measurement http://www.ebi.ac.uk/efo/EFO_0800658 GCST90202628 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Delta-CEHC levels 87 East Asian ancestry individuals NA Affymetrix [4218513] (imputed) 0 delta-CEHC measurement http://www.ebi.ac.uk/efo/EFO_0800174 GCST90202629 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (2) levels 95 East Asian ancestry individuals NA Affymetrix [4272966] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90202630 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,N6-dimethyllysine levels 103 East Asian ancestry individuals NA Affymetrix [4302395] (imputed) 0 N6,N6-dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800100 GCST90202631 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl phenylalanine levels 103 East Asian ancestry individuals NA Affymetrix [4298757] (imputed) 0 1-carboxyethylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800101 GCST90202632 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (1) levels 89 East Asian ancestry individuals NA Affymetrix [4197917] (imputed) 0 sulfate of piperine metabolite C18H21NO3 (1) measurement http://www.ebi.ac.uk/efo/EFO_0801036 GCST90202633 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (5) levels 74 East Asian ancestry individuals NA Affymetrix [4280719] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (5) measurement http://www.ebi.ac.uk/efo/EFO_0801033 GCST90202634 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,2'-Methylenebis(6-tert-butyl-p-cresol) levels 95 East Asian ancestry individuals NA Affymetrix [4268324] (imputed) 0 blood 2,2'-Methylenebis(6-tert-butyl-p-cresol) measurement http://www.ebi.ac.uk/efo/EFO_0022208 GCST90202635 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl isoleucine levels 100 East Asian ancestry individuals NA Affymetrix [4359872] (imputed) 0 1-carboxyethylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800105 GCST90202636 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl valine levels 102 East Asian ancestry individuals NA Affymetrix [4315479] (imputed) 0 1-carboxyethylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800103 GCST90202637 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxysebacate levels 96 East Asian ancestry individuals NA Affymetrix [4256425] (imputed) 0 2-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800571 GCST90202638 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (3) levels 74 East Asian ancestry individuals NA Affymetrix [4284788] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801031 GCST90202639 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetoylcarnitine levels 91 East Asian ancestry individuals NA Affymetrix [4331996] (imputed) 0 indoleacetoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800106 GCST90202640 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (3) levels 92 East Asian ancestry individuals NA Affymetrix [4328520] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90202641 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (4) levels 95 East Asian ancestry individuals NA Affymetrix [4274376] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90202642 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl tyrosine levels 81 East Asian ancestry individuals NA Affymetrix [4354204] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202643 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethyl beta-glucopyranoside levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 ethyl beta-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0801028 GCST90202644 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Allantoin levels 103 East Asian ancestry individuals NA Affymetrix [4300510] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90202720 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xanthine levels 102 East Asian ancestry individuals NA Affymetrix [4317332] (imputed) 0 xanthine measurement http://www.ebi.ac.uk/efo/EFO_0010548 GCST90202721 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sarcosine levels 103 East Asian ancestry individuals NA Affymetrix [4303061] (imputed) 0 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90202722 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantothenate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90202723 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerate levels 103 East Asian ancestry individuals NA Affymetrix [4302331] (imputed) 0 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90202724 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphoethanolamine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90202725 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-oxoproline levels 103 East Asian ancestry individuals NA Affymetrix [4301928] (imputed) 0 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90202726 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (2) levels 103 East Asian ancestry individuals NA Affymetrix [4298993] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202727 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin (z,z) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202728 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erucate (22:1n9) levels 103 East Asian ancestry individuals NA Affymetrix [4300510] (imputed) 0 erucate (22:1n9) measurement http://www.ebi.ac.uk/efo/EFO_0800601 GCST90202729 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylvaline levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-acetylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800117 GCST90202730 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ureidopropionate levels 99 East Asian ancestry individuals NA Affymetrix [4196188] (imputed) 0 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90202731 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thyroxine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90202732 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ursodeoxycholate levels 97 East Asian ancestry individuals NA Affymetrix [4227680] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90202733 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-alanine levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90202734 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylleucine levels 103 East Asian ancestry individuals NA Affymetrix [4302683] (imputed) 0 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90202735 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltyrosine levels 102 East Asian ancestry individuals NA Affymetrix [4322154] (imputed) 0 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90202736 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylmethionine levels 100 East Asian ancestry individuals NA Affymetrix [4352901] (imputed) 0 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90202737 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl indole-3-acetate levels 71 East Asian ancestry individuals NA Affymetrix [4359141] (imputed) 0 methyl indole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0801063 GCST90202738 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillylmandelate (VMA) levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90202739 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyisobutyrate levels 102 East Asian ancestry individuals NA Affymetrix [4319728] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90202740 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-aminoisobutyrate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90202741 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-tocopherol levels 103 East Asian ancestry individuals NA Affymetrix [4299978] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90202742 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urate levels 103 East Asian ancestry individuals NA Affymetrix [4300510] (imputed) 0 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90202743 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetamidobutanoate levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90202744 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:2/24:1, d18:1/24:2) levels 103 East Asian ancestry individuals NA Affymetrix [4299978] (imputed) 0 glycosyl ceramide (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0800532 GCST90202545 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphingadienine (d18:2/16:0) levels 98 East Asian ancestry individuals NA Affymetrix [4212953] (imputed) 0 N-palmitoyl-sphingadienine (d18:2/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800516 GCST90202546 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/24:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800517 GCST90202547 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) levels 99 East Asian ancestry individuals NA Affymetrix [4196715] (imputed) 0 glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800533 GCST90202548 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800520 GCST90202549 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingadienine levels 62 East Asian ancestry individuals NA Affymetrix [4351217] (imputed) 0 sphingadienine measurement http://www.ebi.ac.uk/efo/EFO_0800526 GCST90202550 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingadienine (d18:2/18:0) levels 92 East Asian ancestry individuals NA Affymetrix [4310894] (imputed) 0 N-stearoyl-sphingadienine (d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800521 GCST90202551 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] levels 98 East Asian ancestry individuals NA Affymetrix [4215189] (imputed) 0 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800500 GCST90202552 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] levels 100 East Asian ancestry individuals NA Affymetrix [4351242] (imputed) 0 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800499 GCST90202553 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-heptadecasphingosine (d17:1/16:0) levels 85 East Asian ancestry individuals NA Affymetrix [4260871] (imputed) 0 N-palmitoyl-heptadecasphingosine (d17:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800531 GCST90202554 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:1/23:1, d17:1/24:1) levels 70 East Asian ancestry individuals NA Affymetrix [4395102] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90202555 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-oleoylserine levels 95 East Asian ancestry individuals NA Affymetrix [4275601] (imputed) 0 N-oleoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800525 GCST90202556 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/17:0, d17:1/18:0) levels 75 East Asian ancestry individuals NA Affymetrix [4269431] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90202557 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-tricosanoyl-sphingadienine (d18:2/23:0) levels 96 East Asian ancestry individuals NA Affymetrix [4245601] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90202558 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcholine levels 87 East Asian ancestry individuals NA Affymetrix [4230550] (imputed) 0 stearoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800534 GCST90202559 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/14:0, d16:1/16:0) levels 86 East Asian ancestry individuals NA Affymetrix [4235369] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90202560 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/20:0, d16:0/22:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202561 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-alpha-lysine levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90202562 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoylcholine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 linoleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800535 GCST90202563 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanesulfonate (PFOS) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 perfluorooctanesulfonate (PFOS) measurement http://www.ebi.ac.uk/efo/EFO_0801018 GCST90202564 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/21:0, d16:2/23:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202565 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/19:0, d19:1/18:0) levels 103 East Asian ancestry individuals NA Affymetrix [4298993] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202566 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/24:2) levels 102 East Asian ancestry individuals NA Affymetrix [4319028] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202567 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/18:1) levels 103 East Asian ancestry individuals NA Affymetrix [4298665] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202568 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ximenoylcarnitine (C26:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 ximenoylcarnitine (C26:1) measurement http://www.ebi.ac.uk/efo/EFO_0800543 GCST90202569 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (2) levels 60 East Asian ancestry individuals NA Affymetrix [4378338] (imputed) 0 2-methoxyhydroquinone sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801062 GCST90202695 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-succinyl-phenylalanine levels 91 East Asian ancestry individuals NA Affymetrix [4345898] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202696 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis 3,4-methyleneheptanoate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90202697 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (1) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202698 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,4-di-tert-butylphenol levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 blood 2,4-di-tert-butylphenol measurement http://www.ebi.ac.uk/efo/EFO_0022221 GCST90202699 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylglycine levels 102 East Asian ancestry individuals NA Affymetrix [4322752] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202700 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (2) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202701 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid 12-sulfate levels 90 East Asian ancestry individuals NA Affymetrix [4367630] (imputed) 0 deoxycholic acid (12 or 24)-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800599 GCST90202702 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (2 or 3)-decenoate (10:1n7 or n8) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 (2 or 3)-decenoate (10:1n7 or n8) measurement http://www.ebi.ac.uk/efo/EFO_0800594 GCST90202703 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminoadipate levels 92 East Asian ancestry individuals NA Affymetrix [4315137] (imputed) 0 blood N-acetyl-2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0022202 GCST90202704 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (1) levels 89 East Asian ancestry individuals NA Affymetrix [4182301] (imputed) 0 2-methoxyhydroquinone sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801061 GCST90202705 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels 103 East Asian ancestry individuals NA Affymetrix [4302114] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0800662 GCST90202706 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decadienedioic acid (C10:2-DC) levels 102 East Asian ancestry individuals NA Affymetrix [4321465] (imputed) 0 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90202707 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (3) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202708 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (1) levels 103 East Asian ancestry individuals NA Affymetrix [4301844] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202709 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pipecolate levels 102 East Asian ancestry individuals NA Affymetrix [4316177] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90202710 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202711 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (4) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202712 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202713 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (3) levels 101 East Asian ancestry individuals NA Affymetrix [4337480] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202714 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (1) levels 102 East Asian ancestry individuals NA Affymetrix [4314941] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202715 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinate levels 95 East Asian ancestry individuals NA Affymetrix [4260505] (imputed) 0 picolinate measurement http://www.ebi.ac.uk/efo/EFO_0800115 GCST90202716 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-4-hydroxyproline levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90202717 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetrahydrocortisol glucuronide levels 101 East Asian ancestry individuals NA Affymetrix [4333758] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202718 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (1) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90202719 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2779) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279000 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_278) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279001 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2933) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279041 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2942) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279042 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2945) (2S-amino-3R4R5S14R-tetrahydroxyeicos-6E-enoic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 level of Sphingofungin B in blood serum http://purl.obolibrary.org/obo/OBA_2045049 GCST90279043 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_295) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279044 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2957) (Uranyl acetate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 uranyl acetate measurement http://www.ebi.ac.uk/efo/EFO_0803531 GCST90279045 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_296) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279046 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2972) (N-octadecanoyl-taurine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of N-stearoyltaurine in blood serum http://purl.obolibrary.org/obo/OBA_2045036 GCST90279047 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2977) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279048 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2978) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279049 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2982) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279050 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2983) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279051 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2986) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279052 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_3000) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279053 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2783) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279002 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2784) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279003 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2787) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279004 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2790) (Chlorophacinone) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 chlorophacinone measurement http://www.ebi.ac.uk/efo/EFO_0803489 GCST90279005 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2791) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279006 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2793) (Tsangane L 3-glucoside) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tsangane l 3-glucoside measurement http://www.ebi.ac.uk/efo/EFO_0803461 GCST90279007 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2799) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279008 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_280) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279009 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2801) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279010 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2811) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279011 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_192) (25-Dihydro-24-dimethyloxazole) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279790 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1928) ((3S)-3-Hydroxy-L-enduracididine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 (3S)-3-hydroxy-L-enduracididine measurement http://www.ebi.ac.uk/efo/EFO_0803469 GCST90279791 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1945) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279792 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1960) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279793 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1961) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279794 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_197) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279795 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1973) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279796 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1986) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279797 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1992) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279798 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2002) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279799 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2003) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279800 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2009) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279801 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2015) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279802 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2026) (2-Anthramine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279803 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2031) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 73 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279804 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2037) (2-Hydroxyphenanthrene) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279805 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2041) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279806 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2042) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279807 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2046) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279808 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2050) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279809 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2053) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279810 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2059) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279811 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_206) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279812 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2060) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279813 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_2061) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279814 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1702) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279757 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1704) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279758 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1708) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279759 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1716) (Sulforaphane) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 23 sulforaphane measurement http://www.ebi.ac.uk/efo/EFO_0803458 GCST90279760 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1721) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279761 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1738) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279762 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1742) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279763 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1749) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279764 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1759) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279765 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1764) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279766 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1769) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279767 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_177) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279768 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1772) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279769 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1778) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279770 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1779) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279771 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1781) (Theophylline) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90279772 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1804) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279773 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_181) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279774 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_182) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279775 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2628) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278969 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2632) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278970 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2633) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278971 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2634) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278972 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2637) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278973 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2642) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278974 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1385) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279707 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1393) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279708 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1395) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279709 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1399) (Indole ethanol (Tryptophanol)) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 indole ethanol (tryptophanol) measurement http://www.ebi.ac.uk/efo/EFO_0803423 GCST90279710 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1401) (N(6)-Methyllysine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279711 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1410) (4-Hydroxy-2-oxoglutaric acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 4-hydroxy-2-oxoglutaric acid measurement http://www.ebi.ac.uk/efo/EFO_0800316 GCST90279712 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1428) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279713 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1458) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279714 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1459) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279715 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1460) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279716 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1481) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279717 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1485) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279718 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1503) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279719 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1507) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279720 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1509) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279721 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1511) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279722 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1513) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279723 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1516) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279724 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1517) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279725 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1521) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279726 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1522) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279727 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1534) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 17 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279728 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1537) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279729 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1540) (Dichloroacetate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279730 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1561) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279731 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1208) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279682 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1219) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279683 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1225) (Sulfinoalanine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 sulfinoalanine measurement http://www.ebi.ac.uk/efo/EFO_0803457 GCST90279684 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1232) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279685 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1234) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279686 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1240) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279687 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1246) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279688 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1248) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279689 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1251) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279690 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1254) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279691 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1257) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 25 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279692 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1260) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279693 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1262) (Iminodiacetic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279694 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1264) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279695 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_129) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279696 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1311) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279697 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1318) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279698 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1320) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279699 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1348) (3-Pyridylacetic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279700 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1354) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279701 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1367) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279702 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1370) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279703 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1379) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279704 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1381) (N(6)-Methyllysine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279705 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1384) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279706 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1573) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279732 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1575) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279733 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1586) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279734 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1592) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 13 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279735 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1594) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279736 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1600) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279737 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1612) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279738 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1619) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279739 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1621) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279740 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1624) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279741 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1630) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279742 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1637) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279743 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1644) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279744 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1645) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279745 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1648) (L-Theanine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 theanine measurement http://www.ebi.ac.uk/efo/EFO_0800943 GCST90279746 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1651) (NeNe dimethyllysine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 NeNe dimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0803440 GCST90279747 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1658) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279748 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1673) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279749 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1682) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279750 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1683) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279751 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_169) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279752 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1694) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279753 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1697) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279754 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_17) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279755 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1700) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279756 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2813) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279012 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2817) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279013 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2820) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279014 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2829) (Annoglabasin F) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279015 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2836) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279016 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2837) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279017 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2840) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279018 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2841) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279019 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_285) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279020 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2861) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 13 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279021 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2863) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279022 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2867) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279023 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2868) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279024 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2869) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279025 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2876) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279026 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2884) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279027 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2889) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279028 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2891) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279029 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2895) (Armillarivin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279030 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2898) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279031 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2899) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279032 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2906) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279033 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2911) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279034 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2912) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279035 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2914) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279036 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5349) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280404 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5352) (Melleolide M) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 melleolide M measurement http://www.ebi.ac.uk/efo/EFO_0803429 GCST90280405 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5359) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280406 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_537) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280407 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5370) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280408 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5371) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280409 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1105) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279663 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1108) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279664 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1115) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279665 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1117) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279666 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1119) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279667 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1122) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279668 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1124) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279669 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1128) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279670 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1139) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279671 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1144) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279672 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1152) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279673 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1165) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279674 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_118) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279675 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1182) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279676 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1186) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279677 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1189) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279678 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1200) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279679 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1205) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279680 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_1206) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279681 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2643) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278975 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2646) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278976 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_265) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278977 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2652) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278978 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2667) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278979 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2681) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278980 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2686) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278981 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2695) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278982 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2712) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 15 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278983 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2715) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278984 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2717) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278985 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_272) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278986 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2721) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278987 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2722) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278988 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2723) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278989 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2733) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278990 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2734) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278991 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2744) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278992 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2748) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278993 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2749) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278994 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2751) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278995 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2754) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278996 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2759) (24-Dihydroxy-46-dimethoxy-3-prenylchalcone) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278997 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2765) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278998 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2778) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278999 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxy-2-methylpyridine sulfate levels 42 African ancestry individuals NA Affymetrix [7623436] (imputed) 0 5-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801051 GCST90201637 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,5-dichloro-2,6-dihydroxybenzoic acid levels 58 African ancestry individuals NA Affymetrix [7516163] (imputed) 0 3,5-dichloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801054 GCST90201638 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ethylcatechol sulfate (1) levels 40 African ancestry individuals NA Affymetrix [7355345] (imputed) 0 3-ethylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801047 GCST90201639 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Levulinoylcarnitine levels 47 African ancestry individuals NA Affymetrix [7483838] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201640 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoylcarnitine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxydecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800590 GCST90201641 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,6-dihydroxybenzoic acid levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801046 GCST90201642 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 pregnenetriol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800586 GCST90201643 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholic acid 3-sulfate levels 54 African ancestry individuals NA Affymetrix [7655897] (imputed) 0 taurochenodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800584 GCST90201644 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecadienedioate (C14:2-DC) levels 52 African ancestry individuals NA Affymetrix [7749020] (imputed) 0 tetradecadienedioate (C14:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800585 GCST90201645 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylcatechol sulfate (1) levels 54 African ancestry individuals NA Affymetrix [7701347] (imputed) 0 4-acetylcatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801049 GCST90201646 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Undecenoylcarnitine (C11:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 undecenoylcarnitine (C11:1) measurement http://www.ebi.ac.uk/efo/EFO_0800588 GCST90201647 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-succinyl-phenylalanine levels 48 African ancestry individuals NA Affymetrix [7365120] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201648 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentose acid levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 pentose acid measurement http://www.ebi.ac.uk/efo/EFO_0800660 GCST90201649 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylcarnitine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201650 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxy-4-(methylthio)butanoic acid levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-hydroxy-4-(methylthio)butanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800113 GCST90201651 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis 3,4-methyleneheptanoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90201652 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminoadipate levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 blood N-acetyl-2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0022202 GCST90201653 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (2) levels 35 African ancestry individuals NA Affymetrix [7463697] (imputed) 0 2-methoxyhydroquinone sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801062 GCST90201654 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic acid glycine levels 49 African ancestry individuals NA Affymetrix [7369731] (imputed) 0 vanillic acid glycine measurement http://www.ebi.ac.uk/efo/EFO_0801056 GCST90201655 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched chain 14:0 dicarboxylic acid levels 58 African ancestry individuals NA Affymetrix [7515055] (imputed) 0 branched chain 14:0 dicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0800593 GCST90201656 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,4-di-tert-butylphenol levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 blood 2,4-di-tert-butylphenol measurement http://www.ebi.ac.uk/efo/EFO_0022221 GCST90201657 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-carboxyethylcysteine levels 57 African ancestry individuals NA Affymetrix [7535763] (imputed) 0 L-Cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021614 GCST90201658 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0800662 GCST90201659 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decadienedioic acid (C10:2-DC) levels 58 African ancestry individuals NA Affymetrix [7524533] (imputed) 0 decadienedioic acid (C10:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800598 GCST90201660 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (2 or 3)-decenoate (10:1n7 or n8) levels 57 African ancestry individuals NA Affymetrix [7555650] (imputed) 0 (2 or 3)-decenoate (10:1n7 or n8) measurement http://www.ebi.ac.uk/efo/EFO_0800594 GCST90201661 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90203464 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroyl sphingomyelin (d18:1/24:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 lignoceroyl sphingomyelin (d18:1/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800377 GCST90203465 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:2, d18:2/22:1, d16:1/24:2) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203466 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citraconate/glutaconate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 blood glutaconic acid measurement, blood Citraconic acid measurement http://www.ebi.ac.uk/efo/EFO_0022200, http://www.ebi.ac.uk/efo/EFO_0022201 GCST90203467 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabitol/xylitol levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 arabitol measurement http://www.ebi.ac.uk/efo/EFO_0800148 GCST90203468 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate 3-sulfate levels 105 South Asian ancestry individuals NA Affymetrix [4427804] (imputed) 0 glycochenodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800384 GCST90203469 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2,3-benzenetriol sulfate (2) levels 100 South Asian ancestry individuals NA Affymetrix [4523615] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90203470 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosamine/n-acetylgalactosamine levels 102 South Asian ancestry individuals NA Affymetrix [4468376] (imputed) 0 N-acetylgalactosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149 GCST90203471 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans 3,4-methyleneheptanoate levels 97 South Asian ancestry individuals NA Affymetrix [4387819] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90203472 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels 106 South Asian ancestry individuals NA Affymetrix [4414923] (imputed) 0 Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022107 GCST90203473 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-docosahexaenoyl-gpc (16:0/22:6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800391 GCST90203474 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol glucuronide levels 57 South Asian ancestry individuals NA Affymetrix [4337472] (imputed) 0 phenol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800084 GCST90203475 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 107 South Asian ancestry individuals NA Affymetrix [4394422] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800390 GCST90203476 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-gpc (18:0/22:6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800392 GCST90203477 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-gpc (18:0/18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-stearoyl-2-oleoyl-GPC (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800389 GCST90203478 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl ethanolamide levels 95 South Asian ancestry individuals NA Affymetrix [4417909] (imputed) 0 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90203479 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dilinoleoyl-GPC (18:2/18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 1,2-dilinoleoyl-GPC (18:2/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800388 GCST90203480 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90203481 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-oleoyl-GPE (p-18:0/18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800395 GCST90203482 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxybutyrate/2-hydroxyisobutyrate levels 107 South Asian ancestry individuals NA Affymetrix [4392308] (imputed) 0 2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010979 GCST90203483 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoylglycerol (16:1) levels 83 South Asian ancestry individuals NA Affymetrix [4475963] (imputed) 0 1-palmitoleoylglycerol (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800398 GCST90203484 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleate/vaccenate (18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 vaccenate (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800397 GCST90203485 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 palmitoyl dihydrosphingomyelin (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800400 GCST90203486 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800402 GCST90203487 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) levels 106 South Asian ancestry individuals NA Affymetrix [4414923] (imputed) 0 Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022116 GCST90203488 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (3) levels 56 African ancestry individuals NA Affymetrix [7572402] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801035 GCST90201612 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyetiocholanolone glucuronide levels 46 African ancestry individuals NA Affymetrix [7515471] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201613 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-allylcatechol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-allylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801041 GCST90201614 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C16H19NO3 (2) levels 58 African ancestry individuals NA Affymetrix [7522515] (imputed) 0 sulfate of piperine metabolite C16H19NO3 (2) measurement http://www.ebi.ac.uk/efo/EFO_0801034 GCST90201615 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydrocaffeate sulfate (2) levels 44 African ancestry individuals NA Affymetrix [7704898] (imputed) 0 dihydrocaffeate sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801044 GCST90201616 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoylcarnitine (1) levels 59 African ancestry individuals NA Affymetrix [7499235] (imputed) 0 3-hydroxyhexanoylcarnitine (1) measurement http://www.ebi.ac.uk/efo/EFO_0800580 GCST90201617 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lithocholate sulfate (1) levels 57 African ancestry individuals NA Affymetrix [7578617] (imputed) 0 lithocholate sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800579 GCST90201618 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (5) levels 45 African ancestry individuals NA Affymetrix [7635513] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (5) measurement http://www.ebi.ac.uk/efo/EFO_0801033 GCST90201619 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6,N6-dimethyllysine levels 53 African ancestry individuals NA Affymetrix [7633150] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201620 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-naphthol sulfate levels 59 African ancestry individuals NA Affymetrix [7496533] (imputed) 0 2-naphthol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801038 GCST90201621 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (4) levels 59 African ancestry individuals NA Affymetrix [7494771] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (4) measurement http://www.ebi.ac.uk/efo/EFO_0801032 GCST90201622 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid glucuronide levels 57 African ancestry individuals NA Affymetrix [7603913] (imputed) 0 deoxycholic acid glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800575 GCST90201623 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of piperine metabolite C17H21NO3 (3) levels 47 African ancestry individuals NA Affymetrix [7494378] (imputed) 0 glucuronide of piperine metabolite C17H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801031 GCST90201624 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (3) levels 53 African ancestry individuals NA Affymetrix [7754752] (imputed) 0 sulfate of piperine metabolite C18H21NO3 (3) measurement http://www.ebi.ac.uk/efo/EFO_0801037 GCST90201625 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2-acetyl,N6-methyllysine levels 55 African ancestry individuals NA Affymetrix [7612168] (imputed) 0 N2-acetyl,N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800109 GCST90201626 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholic acid sulfate (1) levels 51 African ancestry individuals NA Affymetrix [7801243] (imputed) 0 glycoursodeoxycholic acid sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800578 GCST90201627 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 hydroxypalmitoyl sphingomyelin (d18:1/16:0(OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800583 GCST90201628 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinoyltaurine levels 57 African ancestry individuals NA Affymetrix [7600687] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201629 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-methylpyridine sulfate levels 51 African ancestry individuals NA Affymetrix [7736734] (imputed) 0 3-hydroxy-2-methylpyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801052 GCST90201630 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenedioate (C20:1-DC) levels 56 African ancestry individuals NA Affymetrix [7580978] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201631 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxy-N6,N6,N6-trimethyllysine levels 58 African ancestry individuals NA Affymetrix [7515709] (imputed) 0 hydroxy-N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800112 GCST90201632 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-5-methylthio-4-pentenoate (dmtpa) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2,3-dihydroxy-5-methylthio-4-pentenoate (DMTPA) measurement http://www.ebi.ac.uk/efo/EFO_0800111 GCST90201633 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinoylglycine levels 55 African ancestry individuals NA Affymetrix [7648869] (imputed) 0 picolinoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800592 GCST90201634 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 palmitoyl-sphingosine-phosphoethanolamine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800591 GCST90201635 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenetriol disulfate levels 59 African ancestry individuals NA Affymetrix [7497020] (imputed) 0 pregnenetriol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800587 GCST90201636 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tricosanoyl sphingomyelin (d18:1/23:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 tricosanoyl sphingomyelin (d18:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0800401 GCST90203489 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 Sphingomyelin (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0022117 GCST90203490 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels 107 South Asian ancestry individuals NA Affymetrix [4390659] (imputed) 0 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800403 GCST90203491 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (p-16:0/18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800419 GCST90203492 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-gpc (p-16:0/18:1) levels 106 South Asian ancestry individuals NA Affymetrix [4407907] (imputed) 0 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800420 GCST90203493 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels 105 South Asian ancestry individuals NA Affymetrix [4429999] (imputed) 0 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800413 GCST90203494 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800407 GCST90203495 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-tocopherol/beta-tocopherol levels 107 South Asian ancestry individuals NA Affymetrix [4389278] (imputed) 0 beta-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0800168 GCST90203496 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) levels 107 South Asian ancestry individuals NA Affymetrix [4390659] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800409 GCST90203497 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (p-16:0/20:4) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800417 GCST90203498 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800410 GCST90203499 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl dihydrosphingomyelin (d18:0/22:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 behenoyl dihydrosphingomyelin (d18:0/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800427 GCST90203500 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-palmitoyl-2-palmitoleoyl-GPC(16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800406 GCST90203501 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (p-16:0/18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4391683] (imputed) 0 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800422 GCST90203502 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-gpc (18:0/18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90203503 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800411 GCST90203504 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/18:0, d19:0/17:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203505 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) levels 107 South Asian ancestry individuals NA Affymetrix [4393321] (imputed) 0 Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0022111 GCST90203506 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) levels 102 South Asian ancestry individuals NA Affymetrix [4483470] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800412 GCST90203507 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyindole sulfate levels 76 South Asian ancestry individuals NA Affymetrix [4401929] (imputed) 0 5-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800085 GCST90203508 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800429 GCST90203509 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristoyl dihydrosphingomyelin (d18:0/14:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 myristoyl dihydrosphingomyelin (d18:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800433 GCST90203510 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphinganine (d18:0/16:0) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90203511 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPG (18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 1-linoleoyl-GPG (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800472 GCST90203512 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thioproline levels 106 South Asian ancestry individuals NA Affymetrix [4415553] (imputed) 0 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90203513 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels 107 South Asian ancestry individuals NA Affymetrix [4391683] (imputed) 0 Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022112 GCST90203439 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol glucuronide levels 83 South Asian ancestry individuals NA Affymetrix [4485381] (imputed) 0 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90203440 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 Sphingomyelin (d18:1/20:1, d18:2/20:0) measurement http://www.ebi.ac.uk/efo/EFO_0022110 GCST90203441 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl sphingomyelin (d18:1/22:0) levels 107 South Asian ancestry individuals NA Affymetrix [4395340] (imputed) 0 behenoyl sphingomyelin (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800376 GCST90203442 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylguaiacol sulfate levels 87 South Asian ancestry individuals NA Affymetrix [4404578] (imputed) 0 4-vinylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800998 GCST90203443 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic alcohol sulfate levels 69 South Asian ancestry individuals NA Affymetrix [4324299] (imputed) 0 blood vanillic alcohol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022214 GCST90203444 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabonate/xylonate levels 107 South Asian ancestry individuals NA Affymetrix [4394422] (imputed) 0 arabonate measurement http://www.ebi.ac.uk/efo/EFO_0801066 GCST90203445 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylcarnitine levels 102 South Asian ancestry individuals NA Affymetrix [4487006] (imputed) 0 phenylacetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800686 GCST90203446 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:2, d18:2/20:1, d16:1/22:2) levels 105 South Asian ancestry individuals NA Affymetrix [4429999] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203447 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-hydroxyindole sulfate levels 106 South Asian ancestry individuals NA Affymetrix [4407252] (imputed) 0 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90203448 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methoxyphenol sulfate levels 104 South Asian ancestry individuals NA Affymetrix [4451266] (imputed) 0 4-methoxyphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800080 GCST90203449 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propyl 4-hydroxybenzoate sulfate levels 103 South Asian ancestry individuals NA Affymetrix [4465730] (imputed) 0 propyl 4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801005 GCST90203450 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 Sphingomyelin (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0022109 GCST90203451 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxycatechol sulfate (1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90203452 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 4-sulfate levels 87 South Asian ancestry individuals NA Affymetrix [4398804] (imputed) 0 dopamine 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800081 GCST90203453 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adipoylcarnitine (C6-DC) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 adipoylcarnitine (C6-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800380 GCST90203454 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurodeoxycholic acid 3-sulfate levels 78 South Asian ancestry individuals NA Affymetrix [4353492] (imputed) 0 taurodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800386 GCST90203455 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonanoylcarnitine (C9) levels 96 South Asian ancestry individuals NA Affymetrix [4425412] (imputed) 0 nonanoylcarnitine (C9) measurement http://www.ebi.ac.uk/efo/EFO_0800381 GCST90203456 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/16:0, d18:1/15:0, d16:1/17:0) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203457 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetoylcarnitine levels 92 South Asian ancestry individuals NA Affymetrix [4479971] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203458 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-carbamoylalanine levels 79 South Asian ancestry individuals NA Affymetrix [4316367] (imputed) 0 blood N-carbamoylalanine measurement http://www.ebi.ac.uk/efo/EFO_0022203 GCST90203459 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxycatechol sulfate (2) levels 85 South Asian ancestry individuals NA Affymetrix [4428006] (imputed) 0 3-methoxycatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801010 GCST90203460 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylkynurenine (2) levels 67 South Asian ancestry individuals NA Affymetrix [4366832] (imputed) 0 N-acetylkynurenine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800083 GCST90203461 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3beta-hydroxy-5-cholestenoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3beta-hydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800379 GCST90203462 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 3-o-sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 dopamine 3-O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800082 GCST90203463 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90201824 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free proline levels 59 African ancestry individuals NA Affymetrix [7497462] (imputed) 0 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90201825 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phytanate levels 59 African ancestry individuals NA Affymetrix [7517115] (imputed) 0 phytanate measurement http://www.ebi.ac.uk/efo/EFO_0801065 GCST90201826 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyruvate levels 59 African ancestry individuals NA Affymetrix [7497538] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90201827 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Valine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90201828 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytidine levels 52 African ancestry individuals NA Affymetrix [7745989] (imputed) 0 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90201829 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 alpha-ketobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800140 GCST90201830 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 12,13-DiHOME levels 57 African ancestry individuals NA Affymetrix [7546466] (imputed) 0 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90201831 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytosine levels 45 African ancestry individuals NA Affymetrix [7578683] (imputed) 0 blood cytosine measurement http://www.ebi.ac.uk/efo/EFO_0022213 GCST90201832 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructose levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 fructose measurement http://www.ebi.ac.uk/efo/EFO_0010477 GCST90201833 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonadecanoate (19:0) levels 59 African ancestry individuals NA Affymetrix [7517115] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90201834 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidate (20:0) levels 59 African ancestry individuals NA Affymetrix [7517115] (imputed) 0 arachidate (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800625 GCST90201835 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free asparagine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90201836 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90201837 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caprate (10:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 caprate 10:0 measurement http://www.ebi.ac.uk/efo/EFO_0021101 GCST90201838 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethylglycine levels 59 African ancestry individuals NA Affymetrix [7494771] (imputed) 0 dimethylglycine measurement http://www.ebi.ac.uk/efo/EFO_0010476 GCST90201839 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90201840 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margarate (17:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90201841 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alanine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90201842 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Betaine levels 59 African ancestry individuals NA Affymetrix [7496336] (imputed) 0 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90201843 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyrosine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90201844 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Blood sugar levels 59 African ancestry individuals NA Affymetrix [7491571] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90201845 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pseudouridine levels 58 African ancestry individuals NA Affymetrix [7533486] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90201846 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11315 levels 58 African ancestry individuals NA Affymetrix [7521437] (imputed) 0 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90201847 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphinganine (d18:0/18:0) levels 46 African ancestry individuals NA Affymetrix [7439653] (imputed) 0 N-stearoyl-sphinganine (d18:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800626 GCST90201848 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl isoleucine levels 54 African ancestry individuals NA Affymetrix [7590037] (imputed) 0 1-carboxyethylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800105 GCST90201604 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Metabolonic lactone sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90201662 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dibutyl sulfosuccinate levels 58 African ancestry individuals NA Affymetrix [7516131] (imputed) 0 blood dibutyl sulfosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0022212 GCST90201663 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) measurement http://www.ebi.ac.uk/efo/EFO_0800661 GCST90201664 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-a-amino-omega-caprolactam levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 (S)-a-amino-omega-caprolactam measurement http://www.ebi.ac.uk/efo/EFO_0801055 GCST90201665 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (1) levels 53 African ancestry individuals NA Affymetrix [7691821] (imputed) 0 2-methoxyhydroquinone sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801061 GCST90201666 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid 12-sulfate levels 52 African ancestry individuals NA Affymetrix [7773925] (imputed) 0 deoxycholic acid (12 or 24)-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800599 GCST90201667 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pipecolate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90201668 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201669 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylglycine levels 58 African ancestry individuals NA Affymetrix [7515709] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201670 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantothenate levels 58 African ancestry individuals NA Affymetrix [7516178] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90201671 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (3) levels 58 African ancestry individuals NA Affymetrix [7532404] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201672 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201673 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinate levels 53 African ancestry individuals NA Affymetrix [7781264] (imputed) 0 picolinate measurement http://www.ebi.ac.uk/efo/EFO_0800115 GCST90201674 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201675 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetrahydrocortisol glucuronide levels 58 African ancestry individuals NA Affymetrix [7572254] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201676 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sarcosine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90201677 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (2) levels 59 African ancestry individuals NA Affymetrix [7499281] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201678 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201679 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (4) levels 58 African ancestry individuals NA Affymetrix [7532404] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201680 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H18N2O4 (3) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201681 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-oxoproline levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90201682 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90201683 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine levels 59 African ancestry individuals NA Affymetrix [7491571] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90201797 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoleucine levels 59 African ancestry individuals NA Affymetrix [7491571] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90201798 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11308 levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 X-11308 measurement http://www.ebi.ac.uk/efo/EFO_0800693 GCST90201849 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11372 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-11372 measurement http://www.ebi.ac.uk/efo/EFO_0800694 GCST90201850 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caprylate (8:0) levels 58 African ancestry individuals NA Affymetrix [7525082] (imputed) 0 caprylate 8:0 measurement http://www.ebi.ac.uk/efo/EFO_0021103 GCST90201851 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11381 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90201852 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11478 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90201853 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11444 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90201854 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11632 levels 59 African ancestry individuals NA Affymetrix [7497436] (imputed) 0 X-11632 measurement http://www.ebi.ac.uk/efo/EFO_0800697 GCST90201855 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caproate (6:0) levels 53 African ancestry individuals NA Affymetrix [7633468] (imputed) 0 caproate 6:0 measurement http://www.ebi.ac.uk/efo/EFO_0021102 GCST90201856 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11470 levels 59 African ancestry individuals NA Affymetrix [7497538] (imputed) 0 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90201857 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11483 levels 52 African ancestry individuals NA Affymetrix [7769776] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90201858 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-07765 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90201859 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate levels 58 African ancestry individuals NA Affymetrix [7522934] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90201860 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentadecanoate (15:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 pentadecanoate 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021073 GCST90201861 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90201862 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-10458 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-10458 measurement http://www.ebi.ac.uk/efo/EFO_0800692 GCST90201863 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sucrose levels 59 African ancestry individuals NA Affymetrix [7503003] (imputed) 0 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90201864 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroorotate levels 58 African ancestry individuals NA Affymetrix [7520712] (imputed) 0 dihydroorotate measurement http://www.ebi.ac.uk/efo/EFO_0800647 GCST90201865 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11299 levels 58 African ancestry individuals NA Affymetrix [7560977] (imputed) 0 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90201866 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11787 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-11787 measurement http://www.ebi.ac.uk/efo/EFO_0021258 GCST90201867 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyresorcinol sulfate levels 91 South Asian ancestry individuals NA Affymetrix [4487764] (imputed) 0 2-methoxyresorcinol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801000 GCST90203433 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylparaben sulfate levels 76 South Asian ancestry individuals NA Affymetrix [4385666] (imputed) 0 blood ethylparaben sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022209 GCST90203434 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-acetamidophenol sulfate levels 89 South Asian ancestry individuals NA Affymetrix [4349713] (imputed) 0 2-acetamidophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801001 GCST90203435 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl-4-hydroxybenzoate sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90203436 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eugenol sulfate levels 96 South Asian ancestry individuals NA Affymetrix [4408747] (imputed) 0 eugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800999 GCST90203437 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-dihomo-linolenylglycerol (20:3) levels 76 South Asian ancestry individuals NA Affymetrix [4362294] (imputed) 0 1-dihomo-linolenylglycerol (20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800374 GCST90203438 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nicotinamide levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90201799 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitate (16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90201800 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-1-pyrroline-5-carboxylate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90201801 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myo-inositol levels 59 African ancestry individuals NA Affymetrix [7496246] (imputed) 0 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90201802 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Leucine levels 59 African ancestry individuals NA Affymetrix [7495043] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90201803 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrulline levels 59 African ancestry individuals NA Affymetrix [7491571] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90201804 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hypotaurine levels 58 African ancestry individuals NA Affymetrix [7530732] (imputed) 0 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90201805 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisol levels (plasma) 59 African ancestry individuals NA Affymetrix [7486916] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90201806 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90201807 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine levels 58 African ancestry individuals NA Affymetrix [7535673] (imputed) 0 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90201808 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonine levels 59 African ancestry individuals NA Affymetrix [7491571] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90201809 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan levels 59 African ancestry individuals NA Affymetrix [7497538] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90201810 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristate (14:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90201811 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Uridine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90201812 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-urocanate levels 58 African ancestry individuals NA Affymetrix [7540730] (imputed) 0 trans-urocanate measurement http://www.ebi.ac.uk/efo/EFO_0800138 GCST90201813 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylnicotinamide levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90201814 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate levels 59 African ancestry individuals NA Affymetrix [7494771] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90201815 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine levels 58 African ancestry individuals NA Affymetrix [7518209] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90201816 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pristanate levels 35 African ancestry individuals NA Affymetrix [7613861] (imputed) 0 pristanate measurement http://www.ebi.ac.uk/efo/EFO_0800623 GCST90201817 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urea levels 59 African ancestry individuals NA Affymetrix [7495043] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90201818 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Retinol (Vitamin A) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90201819 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serotonin levels 59 African ancestry individuals NA Affymetrix [7491870] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90201820 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyridoxal levels 59 African ancestry individuals NA Affymetrix [7489731] (imputed) 0 blood pyridoxal measurement http://www.ebi.ac.uk/efo/EFO_0022222 GCST90201821 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90201822 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma lactate levels 59 African ancestry individuals NA Affymetrix [7500737] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90201823 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,N5-diacetylornithine levels 58 African ancestry individuals NA Affymetrix [7515846] (imputed) 0 N2,N5-diacetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800070 GCST90201365 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ferulic acid 4-sulfate levels 56 African ancestry individuals NA Affymetrix [7561546] (imputed) 0 ferulic acid 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800989 GCST90201366 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltaurine levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90201367 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-oleoyl)-GPE (p-18:1) levels 58 African ancestry individuals NA Affymetrix [7541867] (imputed) 0 1-(1-enyl-oleoyl)-GPE (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800359 GCST90201368 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-sulfo-l-tyrosine levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201369 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-hydroxyphenyl)propionate sulfate levels 43 African ancestry individuals NA Affymetrix [7753349] (imputed) 0 3-(3-hydroxyphenyl)propionate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800990 GCST90201370 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylalliin levels 53 African ancestry individuals NA Affymetrix [7701884] (imputed) 0 N-acetylalliin measurement http://www.ebi.ac.uk/efo/EFO_0800987 GCST90201371 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9-hydroxystearate levels 47 African ancestry individuals NA Affymetrix [7466321] (imputed) 0 9-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0800369 GCST90201372 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Etiocholanolone glucuronide levels 58 African ancestry individuals NA Affymetrix [7524112] (imputed) 0 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90201373 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructosyllysine levels 59 African ancestry individuals NA Affymetrix [7546954] (imputed) 0 fructosyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800073 GCST90201374 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPG (16:0) levels 57 African ancestry individuals NA Affymetrix [7511159] (imputed) 0 1-palmitoyl-GPG (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800367 GCST90201375 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 17alpha-hydroxypregnanolone glucuronide levels 43 African ancestry individuals NA Affymetrix [7765641] (imputed) 0 17alpha-hydroxypregnanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800363 GCST90201376 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPG (18:1) levels 52 African ancestry individuals NA Affymetrix [7648939] (imputed) 0 1-oleoyl-GPG (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800366 GCST90201377 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminoheptanoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90201378 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylanthranilic acid levels 54 African ancestry individuals NA Affymetrix [7601740] (imputed) 0 N-formylanthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0800069 GCST90201379 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioylcarnitine (C18:1-DC) levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 octadecenedioylcarnitine (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800370 GCST90201380 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioylcarnitine (C18-DC) levels 57 African ancestry individuals NA Affymetrix [7583262] (imputed) 0 octadecanedioylcarnitine (C18-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800371 GCST90201381 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/14:0, d18:1/14:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:2/14:0, d18:1/14:1) measurement http://www.ebi.ac.uk/efo/EFO_0022114 GCST90201382 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/24:1, d18:2/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0022113 GCST90201383 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl glucopyranoside (alpha + beta) levels 59 African ancestry individuals NA Affymetrix [7496533] (imputed) 0 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90201384 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutarylcarnitine (2) levels 58 African ancestry individuals NA Affymetrix [7532239] (imputed) 0 3-methylglutarylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800074 GCST90201385 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylcarnitine levels 58 African ancestry individuals NA Affymetrix [7520171] (imputed) 0 phenylacetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800686 GCST90201386 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14:1 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90201387 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabonate/xylonate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 arabonate measurement http://www.ebi.ac.uk/efo/EFO_0801066 GCST90201388 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxypyridine sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90201389 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroyl sphingomyelin (d18:1/24:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 lignoceroyl sphingomyelin (d18:1/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800377 GCST90201415 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylparaben sulfate levels 42 African ancestry individuals NA Affymetrix [7674183] (imputed) 0 blood ethylparaben sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022209 GCST90201416 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 3-o-sulfate levels 59 African ancestry individuals NA Affymetrix [7496805] (imputed) 0 dopamine 3-O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800082 GCST90201417 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/16:0, d18:1/15:0, d16:1/17:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201418 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90201419 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3beta-hydroxy-5-cholestenoate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3beta-hydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800379 GCST90201420 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-carbamoylalanine levels 52 African ancestry individuals NA Affymetrix [7666807] (imputed) 0 blood N-carbamoylalanine measurement http://www.ebi.ac.uk/efo/EFO_0022203 GCST90201421 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxycatechol sulfate (1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90201422 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2,3-benzenetriol sulfate (2) levels 50 African ancestry individuals NA Affymetrix [7456359] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90201423 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxycatechol sulfate (2) levels 49 African ancestry individuals NA Affymetrix [7314119] (imputed) 0 3-methoxycatechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801010 GCST90201424 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylkynurenine (2) levels 45 African ancestry individuals NA Affymetrix [7667999] (imputed) 0 N-acetylkynurenine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800083 GCST90201425 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetoylcarnitine levels 46 African ancestry individuals NA Affymetrix [7565189] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201426 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonanoylcarnitine (C9) levels 54 African ancestry individuals NA Affymetrix [7625854] (imputed) 0 nonanoylcarnitine (C9) measurement http://www.ebi.ac.uk/efo/EFO_0800381 GCST90201427 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabitol/xylitol levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 arabitol measurement http://www.ebi.ac.uk/efo/EFO_0800148 GCST90201428 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citraconate/glutaconate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 blood glutaconic acid measurement, blood Citraconic acid measurement http://www.ebi.ac.uk/efo/EFO_0022200, http://www.ebi.ac.uk/efo/EFO_0022201 GCST90201429 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosamine/n-acetylgalactosamine levels 57 African ancestry individuals NA Affymetrix [7604687] (imputed) 0 N-acetylgalactosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149 GCST90201430 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adipoylcarnitine (C6-DC) levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 adipoylcarnitine (C6-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800380 GCST90201431 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. C-glycosyltryptophan levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90201432 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate 3-sulfate levels 59 African ancestry individuals NA Affymetrix [7491571] (imputed) 0 glycochenodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800384 GCST90201433 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol glucuronide levels 31 African ancestry individuals NA Affymetrix [7539581] (imputed) 0 phenol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800084 GCST90201434 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycodeoxycholate 3-sulfate levels 58 African ancestry individuals NA Affymetrix [7549795] (imputed) 0 glycodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800385 GCST90201435 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl ethanolamide levels 53 African ancestry individuals NA Affymetrix [7779661] (imputed) 0 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90201436 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans 3,4-methyleneheptanoate levels 51 African ancestry individuals NA Affymetrix [7767899] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90201437 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dilinoleoyl-GPC (18:2/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1,2-dilinoleoyl-GPC (18:2/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800388 GCST90201438 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-gpc (18:0/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-stearoyl-2-oleoyl-GPC (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800389 GCST90201439 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (p-16:0/20:4) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800417 GCST90201465 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-gpc (p-16:0/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800420 GCST90201466 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels 59 African ancestry individuals NA Affymetrix [7494771] (imputed) 0 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90201467 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0022111 GCST90201468 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl dihydrosphingomyelin (d18:0/22:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 behenoyl dihydrosphingomyelin (d18:0/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800427 GCST90201469 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/18:0, d19:0/17:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201470 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphinganine (d18:0/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-palmitoyl-sphinganine (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800428 GCST90201471 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (p-16:0/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800422 GCST90201472 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamate levels 42 African ancestry individuals NA Affymetrix [7660257] (imputed) 0 phenylacetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800687 GCST90201473 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800429 GCST90201474 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristoyl dihydrosphingomyelin (d18:0/14:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 myristoyl dihydrosphingomyelin (d18:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800433 GCST90201475 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyindole sulfate levels 51 African ancestry individuals NA Affymetrix [7772134] (imputed) 0 5-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800085 GCST90201476 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-oleoyl-2-docosahexaenoyl-GPC (18:1/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800449 GCST90201477 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800439 GCST90201478 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (p-16:0/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800440 GCST90201479 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800443 GCST90201480 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) levels 58 African ancestry individuals NA Affymetrix [7514963] (imputed) 0 1-(1-enyl-palmitoyl)-2-palmitoleoyl-GPC (P-16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800464 GCST90201481 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) levels 58 African ancestry individuals NA Affymetrix [7515740] (imputed) 0 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800450 GCST90201482 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 59 African ancestry individuals NA Affymetrix [7503003] (imputed) 0 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800466 GCST90201483 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 7-alpha-hydroxy-3-oxo-4-cholestenoate 7-Hoca measurement http://www.ebi.ac.uk/efo/EFO_0021116 GCST90202226 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate (n6 DPA; 22:5n6) levels 95 East Asian ancestry individuals NA Affymetrix [4256008] (imputed) 0 docosapentaenoate (n6 DPA; 22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800249 GCST90202227 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homostachydrine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90202228 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroquinone sulfate levels 94 East Asian ancestry individuals NA Affymetrix [4288849] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90202229 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylglycine levels 95 East Asian ancestry individuals NA Affymetrix [4265947] (imputed) 0 isobutyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800029 GCST90202230 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPE (18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800246 GCST90202231 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl-4-hydroxybenzoate sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90201390 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylphenylalanine levels 56 African ancestry individuals NA Affymetrix [7646167] (imputed) 0 N-formylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800075 GCST90201391 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-dihomo-linolenylglycerol (20:3) levels 44 African ancestry individuals NA Affymetrix [7659969] (imputed) 0 1-dihomo-linolenylglycerol (20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800374 GCST90201392 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylguaiacol sulfate levels 52 African ancestry individuals NA Affymetrix [7731256] (imputed) 0 4-methylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800996 GCST90201393 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic alcohol sulfate levels 41 African ancestry individuals NA Affymetrix [7727398] (imputed) 0 blood vanillic alcohol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022214 GCST90201394 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyramine O-sulfate levels 51 African ancestry individuals NA Affymetrix [7874087] (imputed) 0 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90201395 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxychlorothalonil levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-hydroxychlorothalonil measurement http://www.ebi.ac.uk/efo/EFO_0800992 GCST90201396 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels 51 African ancestry individuals NA Affymetrix [7830220] (imputed) 0 5alpha-androstan-3alpha,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800372 GCST90201397 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylguaiacol sulfate levels 55 African ancestry individuals NA Affymetrix [7601025] (imputed) 0 4-vinylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800998 GCST90201398 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillactate levels 58 African ancestry individuals NA Affymetrix [7596400] (imputed) 0 vanillactate measurement http://www.ebi.ac.uk/efo/EFO_0800078 GCST90201399 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 4-sulfate levels 52 African ancestry individuals NA Affymetrix [7718546] (imputed) 0 dopamine 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800081 GCST90201400 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methoxyphenol sulfate levels 58 African ancestry individuals NA Affymetrix [7510928] (imputed) 0 4-methoxyphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800080 GCST90201401 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-hydroxyindole sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90201402 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyresorcinol sulfate levels 33 African ancestry individuals NA Affymetrix [7715097] (imputed) 0 2-methoxyresorcinol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801000 GCST90201403 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Umbelliferone sulfate levels 48 African ancestry individuals NA Affymetrix [7602791] (imputed) 0 umbelliferone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801006 GCST90201404 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propyl 4-hydroxybenzoate sulfate levels 57 African ancestry individuals NA Affymetrix [7552581] (imputed) 0 propyl 4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801005 GCST90201405 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-acetamidophenol sulfate levels 54 African ancestry individuals NA Affymetrix [7638528] (imputed) 0 2-acetamidophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801001 GCST90201406 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol glucuronide levels 56 African ancestry individuals NA Affymetrix [7640248] (imputed) 0 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90201407 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:2, d18:2/22:1, d16:1/24:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201408 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:2, d18:2/20:1, d16:1/22:2) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90201409 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022112 GCST90201410 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0022109 GCST90201411 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eugenol sulfate levels 54 African ancestry individuals NA Affymetrix [7702428] (imputed) 0 eugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800999 GCST90201412 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl sphingomyelin (d18:1/22:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 behenoyl sphingomyelin (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800376 GCST90201413 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/20:1, d18:2/20:0) measurement http://www.ebi.ac.uk/efo/EFO_0022110 GCST90201414 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-docosahexaenoyl-gpc (16:0/22:6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800391 GCST90201440 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-oleoyl-GPE (p-18:0/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800395 GCST90201441 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-gpc (18:0/22:6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800392 GCST90201442 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleate/vaccenate (18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 vaccenate (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800397 GCST90201443 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoylglycerol (16:1) levels 41 African ancestry individuals NA Affymetrix [7760811] (imputed) 0 1-palmitoleoylglycerol (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800398 GCST90201444 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800413 GCST90201445 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022107 GCST90201446 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90201447 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 palmitoyl dihydrosphingomyelin (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800400 GCST90201448 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022116 GCST90201449 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 Sphingomyelin (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0022117 GCST90201450 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800403 GCST90201451 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 1-stearoyl-2-linoleoyl-GPE (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800402 GCST90201452 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-palmitoleoyl-GPC(16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800406 GCST90201453 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-docosahexaenoyl-GPE (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800410 GCST90201454 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800407 GCST90201455 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPE (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800409 GCST90201456 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800411 GCST90201457 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tricosanoyl sphingomyelin (d18:1/23:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 tricosanoyl sphingomyelin (d18:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0800401 GCST90201458 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800412 GCST90201459 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-gpc (18:0/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90201460 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxybutyrate/2-hydroxyisobutyrate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010979 GCST90201461 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-tocopherol/beta-tocopherol levels 59 African ancestry individuals NA Affymetrix [7488161] (imputed) 0 beta-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0800168 GCST90201462 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (p-18:0/20:4) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800415 GCST90201463 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (p-16:0/18:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800419 GCST90201464 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serotonin levels 96 South Asian ancestry individuals NA Affymetrix [4395066] (imputed) 0 serotonin measurement http://www.ebi.ac.uk/efo/EFO_0004846 GCST90203834 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyridoxal levels 106 South Asian ancestry individuals NA Affymetrix [4415427] (imputed) 0 blood pyridoxal measurement http://www.ebi.ac.uk/efo/EFO_0022222 GCST90203835 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurine levels 107 South Asian ancestry individuals NA Affymetrix [4393856] (imputed) 0 taurine measurement http://www.ebi.ac.uk/efo/EFO_0010536 GCST90203836 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Spermidine levels 100 South Asian ancestry individuals NA Affymetrix [4520503] (imputed) 0 spermidine measurement http://www.ebi.ac.uk/efo/EFO_0021802 GCST90203837 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Retinol (Vitamin A) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 retinol measurement http://www.ebi.ac.uk/efo/EFO_0007900 GCST90203838 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylnicotinamide levels 106 South Asian ancestry individuals NA Affymetrix [4415427] (imputed) 0 1-methylnicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0021829 GCST90203839 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine levels 107 South Asian ancestry individuals NA Affymetrix [4392825] (imputed) 0 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90203840 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 serine measurement http://www.ebi.ac.uk/efo/EFO_0009774 GCST90203841 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 salicylate measurement http://www.ebi.ac.uk/efo/EFO_0021161 GCST90203842 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristate (14:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 myristate 14:0 measurement http://www.ebi.ac.uk/efo/EFO_0021067 GCST90203843 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 glutamate measurement http://www.ebi.ac.uk/efo/EFO_0010487 GCST90203844 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-urocanate levels 107 South Asian ancestry individuals NA Affymetrix [4393893] (imputed) 0 trans-urocanate measurement http://www.ebi.ac.uk/efo/EFO_0800138 GCST90203845 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Uridine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 uridine measurement http://www.ebi.ac.uk/efo/EFO_0010546 GCST90203846 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urea levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 urea measurement http://www.ebi.ac.uk/efo/EFO_0011005 GCST90203847 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-deoxyuridine levels 104 South Asian ancestry individuals NA Affymetrix [4449326] (imputed) 0 2'-deoxyuridine measurement http://www.ebi.ac.uk/efo/EFO_0800643 GCST90203848 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Valine levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 valine measurement http://www.ebi.ac.uk/efo/EFO_0009792 GCST90203849 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonine levels 106 South Asian ancestry individuals NA Affymetrix [4407403] (imputed) 0 threonine measurement http://www.ebi.ac.uk/efo/EFO_0009775 GCST90203850 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan levels 106 South Asian ancestry individuals NA Affymetrix [4409086] (imputed) 0 tryptophan measurement http://www.ebi.ac.uk/efo/EFO_0008534 GCST90203851 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Blood sugar levels 106 South Asian ancestry individuals NA Affymetrix [4414437] (imputed) 0 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90203852 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose levels 107 South Asian ancestry individuals NA Affymetrix [4394451] (imputed) 0 mannose measurement http://www.ebi.ac.uk/efo/EFO_0006958 GCST90203853 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021000 GCST90203854 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pseudouridine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 pseudouridine measurement http://www.ebi.ac.uk/efo/EFO_0021126 GCST90203855 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Betaine levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 plasma betaine measurement http://www.ebi.ac.uk/efo/EFO_0007787 GCST90203856 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyruvate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 pyruvate measurement http://www.ebi.ac.uk/efo/EFO_0010117 GCST90203857 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytidine levels 97 South Asian ancestry individuals NA Affymetrix [4387623] (imputed) 0 cytidine measurement http://www.ebi.ac.uk/efo/EFO_0800645 GCST90203858 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xylose levels 90 South Asian ancestry individuals NA Affymetrix [4543288] (imputed) 0 xylose measurement http://www.ebi.ac.uk/efo/EFO_0800153 GCST90203859 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyrosine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 tyrosine measurement http://www.ebi.ac.uk/efo/EFO_0005058 GCST90203860 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alanine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 alanine measurement http://www.ebi.ac.uk/efo/EFO_0009765 GCST90203861 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 12,13-DiHOME levels 104 South Asian ancestry individuals NA Affymetrix [4452217] (imputed) 0 obsolete_12,13-DiHOME measurement http://www.ebi.ac.uk/efo/EFO_0800624 GCST90203862 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate levels 106 South Asian ancestry individuals NA Affymetrix [4414568] (imputed) 0 alpha-ketobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800140 GCST90203863 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margarate (17:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 margarate 17:0 measurement http://www.ebi.ac.uk/efo/EFO_0021066 GCST90203864 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytosine levels 83 South Asian ancestry individuals NA Affymetrix [4480758] (imputed) 0 blood cytosine measurement http://www.ebi.ac.uk/efo/EFO_0022213 GCST90203865 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free asparagine levels 107 South Asian ancestry individuals NA Affymetrix [4393796] (imputed) 0 asparagine measurement http://www.ebi.ac.uk/efo/EFO_0009766 GCST90203866 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maltose levels in coronary artery disease 82 South Asian ancestry individuals NA Affymetrix [4496710] (imputed) 0 Maltose measurement http://www.ebi.ac.uk/efo/EFO_0021649 GCST90203867 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonadecanoate (19:0) levels 107 South Asian ancestry individuals NA Affymetrix [4393945] (imputed) 0 nonadecanoate 19:0 measurement http://www.ebi.ac.uk/efo/EFO_0021069 GCST90203868 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeine levels 100 South Asian ancestry individuals NA Affymetrix [4527837] (imputed) 0 caffeine measurement http://www.ebi.ac.uk/efo/EFO_0021177 GCST90203869 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidate (20:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 arachidate (20:0) measurement http://www.ebi.ac.uk/efo/EFO_0800625 GCST90203870 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroorotate levels 107 South Asian ancestry individuals NA Affymetrix [4394422] (imputed) 0 dihydroorotate measurement http://www.ebi.ac.uk/efo/EFO_0800647 GCST90203871 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphinganine (d18:0/18:0) levels 85 South Asian ancestry individuals NA Affymetrix [4396678] (imputed) 0 N-stearoyl-sphinganine (d18:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800626 GCST90203872 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sucrose levels 100 South Asian ancestry individuals NA Affymetrix [4548535] (imputed) 0 sucrose measurement http://www.ebi.ac.uk/efo/EFO_0010535 GCST90203873 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentadecanoate (15:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 pentadecanoate 15:0 measurement http://www.ebi.ac.uk/efo/EFO_0021073 GCST90203874 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 kynurenate measurement http://www.ebi.ac.uk/efo/EFO_0800141 GCST90203875 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 Alpha ketoglutarate measurement http://www.ebi.ac.uk/efo/EFO_0010457 GCST90203876 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11299 levels 95 South Asian ancestry individuals NA Affymetrix [4441752] (imputed) 0 X-11299 measurement http://www.ebi.ac.uk/efo/EFO_0021222 GCST90203877 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11381 levels 107 South Asian ancestry individuals NA Affymetrix [4391933] (imputed) 0 X-11381 measurement http://www.ebi.ac.uk/efo/EFO_0021228 GCST90203878 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-10458 levels 100 South Asian ancestry individuals NA Affymetrix [4529215] (imputed) 0 X-10458 measurement http://www.ebi.ac.uk/efo/EFO_0800692 GCST90203879 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11308 levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 X-11308 measurement http://www.ebi.ac.uk/efo/EFO_0800693 GCST90203880 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11315 levels 107 South Asian ancestry individuals NA Affymetrix [4394451] (imputed) 0 X-11315 measurement http://www.ebi.ac.uk/efo/EFO_0021223 GCST90203881 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-07765 levels 104 South Asian ancestry individuals NA Affymetrix [4454527] (imputed) 0 X-07765 measurement http://www.ebi.ac.uk/efo/EFO_0021204 GCST90203882 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11372 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-11372 measurement http://www.ebi.ac.uk/efo/EFO_0800694 GCST90203883 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Flavin adenine dinucleotide (FAD) levels 80 South Asian ancestry individuals NA Affymetrix [4563068] (imputed) 0 flavin adenine dinucleotide (FAD) measurement http://www.ebi.ac.uk/efo/EFO_0800177 GCST90203809 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90203810 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystine levels 107 South Asian ancestry individuals NA Affymetrix [4394255] (imputed) 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90203811 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrulline levels 106 South Asian ancestry individuals NA Affymetrix [4412159] (imputed) 0 citrulline measurement http://www.ebi.ac.uk/efo/EFO_0009777 GCST90203812 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine levels 63 South Asian ancestry individuals NA Affymetrix [4502163] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90203813 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isoleucine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 isoleucine measurement http://www.ebi.ac.uk/efo/EFO_0009793 GCST90203814 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-1-pyrroline-5-carboxylate levels 107 South Asian ancestry individuals NA Affymetrix [4395425] (imputed) 0 S-1-pyrroline-5-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800136 GCST90203815 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myo-inositol levels 106 South Asian ancestry individuals NA Affymetrix [4410723] (imputed) 0 myo-inositol measurement http://www.ebi.ac.uk/efo/EFO_0800621 GCST90203816 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisol levels (plasma) 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 cortisol measurement http://www.ebi.ac.uk/efo/EFO_0005843 GCST90203817 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hypotaurine levels 107 South Asian ancestry individuals NA Affymetrix [4391299] (imputed) 0 hypotaurine measurement http://www.ebi.ac.uk/efo/EFO_0021833 GCST90203818 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Leucine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 leucine measurement http://www.ebi.ac.uk/efo/EFO_0009770 GCST90203819 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lysine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90203820 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine levels 107 South Asian ancestry individuals NA Affymetrix [4393796] (imputed) 0 methionine measurement http://www.ebi.ac.uk/efo/EFO_0009771 GCST90203821 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Malate levels 107 South Asian ancestry individuals NA Affymetrix [4392806] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90203822 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitate (16:0) levels 107 South Asian ancestry individuals NA Affymetrix [4390626] (imputed) 0 palmitate 16:0 measurement http://www.ebi.ac.uk/efo/EFO_0021071 GCST90203823 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearate (18:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90203824 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nicotinamide levels 105 South Asian ancestry individuals NA Affymetrix [4427262] (imputed) 0 nicotinamide measurement http://www.ebi.ac.uk/efo/EFO_0800178 GCST90203825 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pristanate levels 67 South Asian ancestry individuals NA Affymetrix [4353277] (imputed) 0 pristanate measurement http://www.ebi.ac.uk/efo/EFO_0800623 GCST90203826 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate levels (UKB data field 30810) 107 South Asian ancestry individuals NA Affymetrix [4396414] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90203827 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotate levels 105 South Asian ancestry individuals NA Affymetrix [4429321] (imputed) 0 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90203828 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylalanine levels 107 South Asian ancestry individuals NA Affymetrix [4393856] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90203829 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phytanate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 phytanate measurement http://www.ebi.ac.uk/efo/EFO_0801065 GCST90203830 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ornithine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90203831 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma free proline levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 proline measurement http://www.ebi.ac.uk/efo/EFO_0009773 GCST90203832 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Plasma lactate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 lactate measurement http://www.ebi.ac.uk/efo/EFO_0007745 GCST90203833 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11470 levels 103 South Asian ancestry individuals NA Affymetrix [4461672] (imputed) 0 X-11470 measurement http://www.ebi.ac.uk/efo/EFO_0021241 GCST90203884 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11444 levels 107 South Asian ancestry individuals NA Affymetrix [4391030] (imputed) 0 X-11444 measurement http://www.ebi.ac.uk/efo/EFO_0021237 GCST90203885 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11478 levels 107 South Asian ancestry individuals NA Affymetrix [4396325] (imputed) 0 X-11478 measurement http://www.ebi.ac.uk/efo/EFO_0021242 GCST90203886 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11632 levels 102 South Asian ancestry individuals NA Affymetrix [4491654] (imputed) 0 X-11632 measurement http://www.ebi.ac.uk/efo/EFO_0800697 GCST90203887 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11795 levels 107 South Asian ancestry individuals NA Affymetrix [4388593] (imputed) 0 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90203888 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11843 levels 79 South Asian ancestry individuals NA Affymetrix [4327980] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90203889 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11483 levels 71 South Asian ancestry individuals NA Affymetrix [4547046] (imputed) 0 X-11483 measurement http://www.ebi.ac.uk/efo/EFO_0021243 GCST90203890 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11847 levels 100 South Asian ancestry individuals NA Affymetrix [4532169] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90203891 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12013 levels 74 South Asian ancestry individuals NA Affymetrix [4444421] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90203892 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11849 levels 102 South Asian ancestry individuals NA Affymetrix [4498271] (imputed) 0 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90203893 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11850 levels 88 South Asian ancestry individuals NA Affymetrix [4362792] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90203894 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11880 levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 X-11880 measurement http://www.ebi.ac.uk/efo/EFO_0800698 GCST90203895 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11858 levels 87 South Asian ancestry individuals NA Affymetrix [4385832] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90203896 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11852 levels 77 South Asian ancestry individuals NA Affymetrix [4373896] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90203897 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12026 levels 107 South Asian ancestry individuals NA Affymetrix [4396352] (imputed) 0 X-12026 measurement http://www.ebi.ac.uk/efo/EFO_0800700 GCST90203898 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12007 levels 107 South Asian ancestry individuals NA Affymetrix [4394978] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90203899 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12127 levels 77 South Asian ancestry individuals NA Affymetrix [4363237] (imputed) 0 X-12127 measurement http://www.ebi.ac.uk/efo/EFO_0800709 GCST90203900 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12104 levels 85 South Asian ancestry individuals NA Affymetrix [4446908] (imputed) 0 X-12104 measurement http://www.ebi.ac.uk/efo/EFO_0800703 GCST90203901 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12112 levels 106 South Asian ancestry individuals NA Affymetrix [4408017] (imputed) 0 X-12112 measurement http://www.ebi.ac.uk/efo/EFO_0800705 GCST90203902 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12101 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90203903 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12216 levels 101 South Asian ancestry individuals NA Affymetrix [4505125] (imputed) 0 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90203904 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12193 levels 98 South Asian ancestry individuals NA Affymetrix [4385932] (imputed) 0 X-12193 measurement http://www.ebi.ac.uk/efo/EFO_0800710 GCST90203905 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12221 levels 82 South Asian ancestry individuals NA Affymetrix [4519584] (imputed) 0 X-12221 measurement http://www.ebi.ac.uk/efo/EFO_0800711 GCST90203906 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12306 levels 82 South Asian ancestry individuals NA Affymetrix [4502734] (imputed) 0 X-12306 measurement http://www.ebi.ac.uk/efo/EFO_0800714 GCST90203907 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linolenoyl-GPC (18:3) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-linolenoyl-GPC (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800354 GCST90201364 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2433) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278939 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2434) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278940 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2438) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278941 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2445) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278942 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2451) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278943 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2455) (11-111-Undecanediylbis(oxy)bisbenzene) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278944 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2457) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278945 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2469) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278946 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_247) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278947 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_248) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278948 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2485) (5(6)-Pentyl-14-dioxan-2-one) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 5(6)-pentyl-14-dioxan-2-one measurement http://www.ebi.ac.uk/efo/EFO_0803397 GCST90278949 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2497) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278950 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2501) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278951 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2505) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278952 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2511) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278953 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2515) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278954 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2526) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278955 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2535) (Tridecyl phloretate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278956 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2547) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278957 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_255) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278958 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2552) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278959 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2563) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278960 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2588) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278961 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2589) (4-Hydroxybenzyl isothiocyanate 4-acetylrhamnoside) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 4-hydroxybenzyl isothiocyanate 4-acetylrhamnoside measurement http://www.ebi.ac.uk/efo/EFO_0803391 GCST90278962 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2603) (5-hydroperoxy-7-35-epidioxy-2-(2-octenyl)-cyclopentyl-6-heptenoic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of 5-hydroperoxy-7-[3,5-epidioxy-2-(2-octenyl)-cyclopentyl]-6-heptenoic acid in blood serum http://purl.obolibrary.org/obo/OBA_2045048 GCST90278963 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2008) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278870 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2012) ((9Z12Z14E)-16-Hydroxy-91214-octadecatrienoic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 9 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278871 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2019) (1213-Epoxy-915-octadecadienoic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278872 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2022) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278873 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2028) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278874 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2030) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278875 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2036) (Antimony(III) isopropoxide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 antimony(III) isopropoxide measurement http://www.ebi.ac.uk/efo/EFO_0803524 GCST90278876 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2042) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278877 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2047) (Sodium nitroprusside dihydrate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 sodium nitroprusside dihydrate measurement http://www.ebi.ac.uk/efo/EFO_0803515 GCST90278878 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2056) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278879 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2057) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278880 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2058) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278881 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_206) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278882 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2068) (Methylmercuric dicyanamide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 methylmercuric dicyanamide measurement http://www.ebi.ac.uk/efo/EFO_0803528 GCST90278883 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_207) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278884 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2072) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278885 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2090) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 13 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278886 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2092) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278887 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2105) (alpha-Ethyl-alphabeta-diphenyl-2-pyridineethanol) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 alpha-ethyl-alphabeta-diphenyl-2-pyridineethanol measurement http://www.ebi.ac.uk/efo/EFO_0803482 GCST90278888 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2110) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278889 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2112) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278890 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2116) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278891 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2129) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278892 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2130) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278893 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2133) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278894 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2137) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278895 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2138) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278896 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2152) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278897 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2154) (N-Acetylneuraminate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90278898 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2161) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278899 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2177) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278900 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2179) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278901 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2188) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278902 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_220) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278903 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2207) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278904 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2212) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278905 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2217) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 17 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278906 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2219) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278907 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2233) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278908 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2235) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278909 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1013) (N-Acetylhistidine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90278689 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1018) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278690 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1027) (Vanillylmandelate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90278691 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1044) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278692 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1050) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278693 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1058) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278694 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1060) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278695 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1061) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278696 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1068) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278697 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1070) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278698 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5386) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280412 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5387) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 11 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280413 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5408) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280414 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5412) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280415 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5421) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280416 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5429) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 20 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280417 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_543) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280418 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5448) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280419 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5452) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280420 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5453) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280421 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5455) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 13 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280422 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5460) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280423 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5462) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280424 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5465) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280425 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5468) (Indol-3-ylacetyl-myo-inositol L-arabinoside) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 indol-3-ylacetyl-myo-inositol L-arabinoside measurement http://www.ebi.ac.uk/efo/EFO_0803501 GCST90280426 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5471) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280427 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5473) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280428 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5474) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280429 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5495) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280430 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5506) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280431 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5508) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280432 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_551) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280433 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5510) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280434 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5514) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280435 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5515) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280436 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1179) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278724 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_118) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278725 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1189) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278726 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1192) (Glucose) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 glucose measurement http://www.ebi.ac.uk/efo/EFO_0004468 GCST90278727 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1194) (Tyramine-O-sulfate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90278728 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1196) (Tyramine-O-sulfate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90278729 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1200) (Tyramine-O-sulfate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90278730 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1206) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278731 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1208) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278732 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1209) (Tyrosol 4-sulfate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 tyrosol 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0803462 GCST90278733 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1210) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278734 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1213) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278735 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1267) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278745 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1271) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278746 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1216) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278736 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1221) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278737 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1225) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278738 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1240) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278739 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1242) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278740 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_126) (Potassium bicarbonate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 potassium bicarbonate measurement http://www.ebi.ac.uk/efo/EFO_0803509 GCST90278741 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1261) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278742 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1264) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278743 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1266) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278744 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5375) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280410 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5385) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280411 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2276) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278914 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2282) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278915 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2299) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278916 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2303) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278917 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_231) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278918 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2319) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 20 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278919 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2342) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278920 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2344) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278921 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2345) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278922 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2347) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278923 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2369) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278924 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_237) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278925 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2373) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278926 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2384) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278927 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2394) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278928 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2397) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278929 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2400) (Carpropamid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 carpropamid measurement http://www.ebi.ac.uk/efo/EFO_0803487 GCST90278930 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2403) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278931 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2404) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278932 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2405) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278933 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2408) (Lormetazepam) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 lormetazepam measurement http://www.ebi.ac.uk/efo/EFO_0803465 GCST90278934 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2414) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278935 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2415) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278936 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_242) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278937 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2430) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278938 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5516) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280437 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5518) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280438 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5522) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280439 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5523) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280440 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5528) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280441 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_555) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280442 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5550) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280443 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5556) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280444 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5565) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280445 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5582) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280446 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5586) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280447 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_56) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280448 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_560) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280449 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5601) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280450 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5603) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280451 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5605) (15-Acetoxyscirpene-34-diol 4-O-a-D-glucopyranoside) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 15-acetoxyscirpene-34-diol 4-O-a-D-glucopyranoside measurement http://www.ebi.ac.uk/efo/EFO_0803385 GCST90280452 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_561) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280453 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5611) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280454 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5616) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280455 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5622) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 20 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280456 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5629) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280457 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_563) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280458 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5631) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280459 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5642) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280460 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_5643) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280461 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_261) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278964 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2613) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278965 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2615) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278966 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2621) (Azothoate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 azothoate measurement http://www.ebi.ac.uk/efo/EFO_0803485 GCST90278967 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2623) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278968 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1864) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278850 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1870) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278851 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1885) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278852 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1893) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278853 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1900) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278854 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1902) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278855 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1905) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278856 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1911) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278857 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1920) (Myristoylglycine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 myristoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0803434 GCST90278858 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1928) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278859 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1935) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278860 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1941) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278861 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1951) (6-Hydroxypentadecanedioic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 6-hydroxypentadecanedioic acid measurement http://www.ebi.ac.uk/efo/EFO_0803399 GCST90278862 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1962) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278863 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1971) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278864 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1980) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278865 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1993) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278866 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_20) (Pyruvic acid) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 pyruvic acid measurement http://www.ebi.ac.uk/efo/EFO_0801217 GCST90278867 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2003) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278868 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_2005) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278869 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1074) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278699 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1075) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278700 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1077) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278701 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1078) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278702 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1091) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278703 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1095) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278704 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1100) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278705 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1104) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278706 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1109) (Quinoclamin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 quinoclamin measurement http://www.ebi.ac.uk/efo/EFO_0803510 GCST90278707 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1113) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278708 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_112) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278709 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1120) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278710 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1125) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278711 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1128) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278712 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1137) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278713 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1138) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278714 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1145) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278715 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1146) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278716 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1150) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278717 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1154) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278718 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1155) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278719 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1157) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278720 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_116) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278721 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1161) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278722 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_1162) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90278723 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylalliin levels 88 South Asian ancestry individuals NA Affymetrix [4353949] (imputed) 0 N-acetylalliin measurement http://www.ebi.ac.uk/efo/EFO_0800987 GCST90203408 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acisoga levels 100 South Asian ancestry individuals NA Affymetrix [4531097] (imputed) 0 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90203409 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-piperidinone levels 107 South Asian ancestry individuals NA Affymetrix [4389263] (imputed) 0 2-piperidinone measurement http://www.ebi.ac.uk/efo/EFO_0800980 GCST90203410 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,N5-diacetylornithine levels 99 South Asian ancestry individuals NA Affymetrix [4341226] (imputed) 0 N2,N5-diacetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800070 GCST90203411 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltaurine levels 105 South Asian ancestry individuals NA Affymetrix [4430704] (imputed) 0 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90203412 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 Sphingomyelin (d18:1/24:1, d18:2/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0022113 GCST90203413 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 17alpha-hydroxypregnanolone glucuronide levels 65 South Asian ancestry individuals NA Affymetrix [4445661] (imputed) 0 17alpha-hydroxypregnanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800363 GCST90203414 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioylcarnitine (C18:1-DC) levels 107 South Asian ancestry individuals NA Affymetrix [4400002] (imputed) 0 octadecenedioylcarnitine (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800370 GCST90203415 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutarylcarnitine (2) levels 107 South Asian ancestry individuals NA Affymetrix [4392767] (imputed) 0 3-methylglutarylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800074 GCST90203416 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14:1 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90203417 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPG (16:0) levels 98 South Asian ancestry individuals NA Affymetrix [4374095] (imputed) 0 1-palmitoyl-GPG (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800367 GCST90203418 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels 72 South Asian ancestry individuals NA Affymetrix [4518726] (imputed) 0 5alpha-androstan-3alpha,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800372 GCST90203419 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/14:0, d18:1/14:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 Sphingomyelin (d18:2/14:0, d18:1/14:1) measurement http://www.ebi.ac.uk/efo/EFO_0022114 GCST90203420 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylphenylalanine levels 100 South Asian ancestry individuals NA Affymetrix [4521692] (imputed) 0 N-formylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800075 GCST90203421 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxychlorothalonil levels 107 South Asian ancestry individuals NA Affymetrix [4392870] (imputed) 0 4-hydroxychlorothalonil measurement http://www.ebi.ac.uk/efo/EFO_0800992 GCST90203422 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl glucopyranoside (alpha + beta) levels 103 South Asian ancestry individuals NA Affymetrix [4471037] (imputed) 0 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90203423 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioylcarnitine (C18-DC) levels 104 South Asian ancestry individuals NA Affymetrix [4449892] (imputed) 0 octadecanedioylcarnitine (C18-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800371 GCST90203424 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylguaiacol sulfate levels 81 South Asian ancestry individuals NA Affymetrix [4530687] (imputed) 0 4-methylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800996 GCST90203425 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyramine O-sulfate levels 90 South Asian ancestry individuals NA Affymetrix [4519405] (imputed) 0 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90203426 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ferulic acid 4-sulfate levels 96 South Asian ancestry individuals NA Affymetrix [4409233] (imputed) 0 ferulic acid 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800989 GCST90203427 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxypyridine sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4395332] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90203428 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-hydroxyphenyl)propionate sulfate levels 68 South Asian ancestry individuals NA Affymetrix [4319912] (imputed) 0 3-(3-hydroxyphenyl)propionate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800990 GCST90203429 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Etiocholanolone glucuronide levels 99 South Asian ancestry individuals NA Affymetrix [4346583] (imputed) 0 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90203430 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9-hydroxystearate levels 95 South Asian ancestry individuals NA Affymetrix [4434142] (imputed) 0 9-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0800369 GCST90203431 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinimide levels 72 South Asian ancestry individuals NA Affymetrix [4540349] (imputed) 0 blood succinimide measurement http://www.ebi.ac.uk/efo/EFO_0022211 GCST90203382 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethyl sulfone levels 105 South Asian ancestry individuals NA Affymetrix [4431728] (imputed) 0 dimethyl sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800979 GCST90203383 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycohyocholate levels 96 South Asian ancestry individuals NA Affymetrix [4404892] (imputed) 0 glycohyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800346 GCST90203384 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margaroylcarnitine (C17) levels 104 South Asian ancestry individuals NA Affymetrix [4452774] (imputed) 0 margaroylcarnitine (C17) measurement http://www.ebi.ac.uk/efo/EFO_0800345 GCST90203385 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (R)-3-hydroxybutyrylcarnitine levels 104 South Asian ancestry individuals NA Affymetrix [4453116] (imputed) 0 (R)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800344 GCST90203386 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine betaine (hercynine) levels 96 South Asian ancestry individuals NA Affymetrix [4394647] (imputed) 0 histidine betaine (hercynine) measurement http://www.ebi.ac.uk/efo/EFO_0800972 GCST90203387 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyltaurine levels 83 South Asian ancestry individuals NA Affymetrix [4480849] (imputed) 0 N-methyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800064 GCST90203388 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcarnosine levels 106 South Asian ancestry individuals NA Affymetrix [4416200] (imputed) 0 blood N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022217 GCST90203389 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alliin levels 96 South Asian ancestry individuals NA Affymetrix [4382175] (imputed) 0 alliin measurement http://www.ebi.ac.uk/efo/EFO_0800970 GCST90203390 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-stearoyl-GPE (18:0) levels 106 South Asian ancestry individuals NA Affymetrix [4407646] (imputed) 0 2-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800343 GCST90203391 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolin-2-one levels 79 South Asian ancestry individuals NA Affymetrix [4334384] (imputed) 0 indolin-2-one measurement http://www.ebi.ac.uk/efo/EFO_0800981 GCST90203392 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-oxopiperidine-2-carboxylate levels 100 South Asian ancestry individuals NA Affymetrix [4532114] (imputed) 0 6-oxopiperidine-2-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800066 GCST90203393 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-sulfo-l-tyrosine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203394 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-acetylphenol sulfate levels 74 South Asian ancestry individuals NA Affymetrix [4447948] (imputed) 0 3-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800983 GCST90203395 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminophenol sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90203396 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 Sphingomyelin (d18:1/14:0, d16:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022105 GCST90203397 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 Sphingomyelin (d18:2/16:0, d18:1/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0022115 GCST90203398 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-delta-acetylornithine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90203399 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxytyramine sulfate levels 68 South Asian ancestry individuals NA Affymetrix [4374104] (imputed) 0 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90203400 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linolenoyl-GPC (18:3) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-linolenoyl-GPC (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800354 GCST90203401 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-oleoyl)-GPE (p-18:1) levels 107 South Asian ancestry individuals NA Affymetrix [4391565] (imputed) 0 1-(1-enyl-oleoyl)-GPE (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800359 GCST90203402 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminoheptanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90203403 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-allylcysteine levels 99 South Asian ancestry individuals NA Affymetrix [4332903] (imputed) 0 S-allylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800985 GCST90203404 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructosyllysine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 fructosyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800073 GCST90203405 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfone levels 107 South Asian ancestry individuals NA Affymetrix [4392767] (imputed) 0 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90203406 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-o-methylascorbic acid levels 107 South Asian ancestry individuals NA Affymetrix [4389019] (imputed) 0 2-O-methylascorbic acid measurement http://www.ebi.ac.uk/efo/EFO_0800164 GCST90203357 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole propionate levels 103 South Asian ancestry individuals NA Affymetrix [4456452] (imputed) 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90203358 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnanediol-3-glucuronide levels 100 South Asian ancestry individuals NA Affymetrix [4530010] (imputed) 0 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90203359 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-citrylglutamate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90203360 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carboxyethyl-gaba levels 104 South Asian ancestry individuals NA Affymetrix [4446244] (imputed) 0 carboxyethyl-GABA measurement http://www.ebi.ac.uk/efo/EFO_0800059 GCST90203361 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulate levels 75 South Asian ancestry individuals NA Affymetrix [4390707] (imputed) 0 dihydroferulate measurement http://www.ebi.ac.uk/efo/EFO_0800969 GCST90203362 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trimethylamine n-oxide levels 106 South Asian ancestry individuals NA Affymetrix [4409082] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90203363 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-methyllysine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90203364 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPC (p-16:0) levels 107 South Asian ancestry individuals NA Affymetrix [4390626] (imputed) 0 1-(1-enyl-palmitoyl)-GPC (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800323 GCST90203365 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-lignoceroyl-GPC (24:0) levels 106 South Asian ancestry individuals NA Affymetrix [4415444] (imputed) 0 1-lignoceroyl-GPC (24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800322 GCST90203366 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholate levels 107 South Asian ancestry individuals NA Affymetrix [4390947] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90203367 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPE (p-16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-(1-enyl-palmitoyl)-GPE (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800334 GCST90203368 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosanedioate (C20-DC) levels 107 South Asian ancestry individuals NA Affymetrix [4390812] (imputed) 0 eicosanedioate (C20-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800330 GCST90203369 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl-linoleoyl-glycerol (18:1/18:2) [2] levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 oleoyl-linoleoyl-glycerol (18:1/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800333 GCST90203370 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine sulfoxide levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 S-methylcysteine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0800058 GCST90203371 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-4-decenoate (10:1n6) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 cis-4-decenoate (10:1n6) measurement http://www.ebi.ac.uk/efo/EFO_0800318 GCST90203372 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannonate levels 106 South Asian ancestry individuals NA Affymetrix [4413970] (imputed) 0 mannonate measurement http://www.ebi.ac.uk/efo/EFO_0800971 GCST90203373 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lanthionine levels 101 South Asian ancestry individuals NA Affymetrix [4506581] (imputed) 0 lanthionine measurement http://www.ebi.ac.uk/efo/EFO_0800063 GCST90203374 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminooctanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90203375 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxydecanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800347 GCST90203376 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylcatechol sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4393856] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90203377 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC glucuronide levels 79 South Asian ancestry individuals NA Affymetrix [4318192] (imputed) 0 gamma-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800165 GCST90203378 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (2) levels 65 South Asian ancestry individuals NA Affymetrix [4417473] (imputed) 0 3-methyl catechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800973 GCST90203379 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (1) levels 105 South Asian ancestry individuals NA Affymetrix [4430132] (imputed) 0 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90203380 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guaiacol sulfate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 guaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800978 GCST90203381 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine to asparagine ratio 8,225 European ancestry individuals NA Affymetrix [15429284] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200989 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Benzoate to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [2] ratio 6,865 European ancestry individuals NA Affymetrix [15370369] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200990 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine to alanine ratio 8,233 European ancestry individuals NA Affymetrix [15429262] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200991 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alanine to asparagine ratio 8,248 European ancestry individuals NA Affymetrix [15431174] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200992 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate to oxalate (ethanedioate) ratio 8,107 European ancestry individuals NA Affymetrix [15425675] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200993 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine to alanine ratio 8,222 European ancestry individuals NA Affymetrix [15429317] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200994 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate to taurocholate ratio 7,614 European ancestry individuals NA Affymetrix [15406772] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200995 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrate to taurocholate ratio 7,618 European ancestry individuals NA Affymetrix [15405901] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200996 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine to glutamine ratio 8,223 European ancestry individuals NA Affymetrix [15429925] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200997 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate to citrate ratio 8,147 European ancestry individuals NA Affymetrix [15428164] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200998 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholate to oxalate (ethanedioate) ratio 7,755 European ancestry individuals NA Affymetrix [15409864] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200999 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine to threonine ratio 8,237 European ancestry individuals NA Affymetrix [15430937] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201000 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Serine to alpha-ketobutyrate ratio 8,100 European ancestry individuals NA Affymetrix [15425506] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201001 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maltose to sucrose ratio 5,984 European ancestry individuals NA Affymetrix [15325380] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201002 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to N-palmitoyl-sphingosine (d18:1 to 16:0) ratio 8,173 European ancestry individuals NA Affymetrix [15428947] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201003 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to N-stearoyl-sphingosine (d18:1 to 18:0) ratio 8,179 European ancestry individuals NA Affymetrix [15428595] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90201004 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl phenylalanine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-carboxyethylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800101 GCST90201602 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoleglyoxylic acid levels 59 African ancestry individuals NA Affymetrix [7569426] (imputed) 0 3-indoleglyoxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0801027 GCST90201603 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl leucine levels 57 African ancestry individuals NA Affymetrix [7555254] (imputed) 0 N-acetyl-l-leucine measurement http://www.ebi.ac.uk/efo/EFO_0021653 GCST90201605 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,2'-Methylenebis(6-tert-butyl-p-cresol) levels 54 African ancestry individuals NA Affymetrix [7677953] (imputed) 0 blood 2,2'-Methylenebis(6-tert-butyl-p-cresol) measurement http://www.ebi.ac.uk/efo/EFO_0022208 GCST90201606 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-lactoyl tyrosine levels 49 African ancestry individuals NA Affymetrix [7468947] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201607 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-ketocaprylate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 2-ketocaprylate measurement http://www.ebi.ac.uk/efo/EFO_0800110 GCST90201608 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 11beta-hydroxyandrosterone glucuronide levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 11beta-hydroxyandrosterone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800573 GCST90201609 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylcatechol sulfate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 4-ethylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801040 GCST90201610 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sulfate of piperine metabolite C18H21NO3 (1) levels 54 African ancestry individuals NA Affymetrix [7735933] (imputed) 0 sulfate of piperine metabolite C18H21NO3 (1) measurement http://www.ebi.ac.uk/efo/EFO_0801036 GCST90201611 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Umbelliferone sulfate levels 81 South Asian ancestry individuals NA Affymetrix [4514501] (imputed) 0 umbelliferone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801006 GCST90203432 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisol to taurocholate ratio 7,610 European ancestry individuals NA Affymetrix [15406285] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200890 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicylate to caprylate (8:0) ratio 8,068 European ancestry individuals NA Affymetrix [15424503] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200891 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hypotaurine to taurine ratio 8,157 European ancestry individuals NA Affymetrix [15428617] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200892 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurine to cysteine ratio 8,186 European ancestry individuals NA Affymetrix [15428569] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200893 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine to theophylline ratio 4,662 European ancestry individuals NA Affymetrix [15451360] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200894 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hypotaurine to cysteine ratio 8,134 European ancestry individuals NA Affymetrix [15427713] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200895 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine to EDTA ratio 4,926 European ancestry individuals NA Affymetrix [15462587] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200896 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theophylline to EDTA ratio 7,867 European ancestry individuals NA Affymetrix [15416936] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200897 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrulline to phosphate ratio 8,294 European ancestry individuals NA Affymetrix [15432024] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200898 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrulline to ornithine ratio 8,225 European ancestry individuals NA Affymetrix [15430340] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200899 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to oleoyl-linoleoyl-glycerol (18:1 to 18:2) [2] ratio 7,992 European ancestry individuals NA Affymetrix [15418831] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200900 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ornithine to phosphate ratio 8,295 European ancestry individuals NA Affymetrix [15432162] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200901 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [2] ratio 7,649 European ancestry individuals NA Affymetrix [15404687] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200902 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to glycerol ratio 8,179 European ancestry individuals NA Affymetrix [15428583] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200903 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [1] ratio 7,623 European ancestry individuals NA Affymetrix [15401520] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200904 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to glycerol ratio 8,160 European ancestry individuals NA Affymetrix [15428243] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200905 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-deoxyuridine to cytidine ratio 7,410 European ancestry individuals NA Affymetrix [15395700] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200906 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Retinol (Vitamin A) to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [1] ratio 7,617 European ancestry individuals NA Affymetrix [15401710] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200907 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Retinol (Vitamin A) to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [2] ratio 7,668 European ancestry individuals NA Affymetrix [15405185] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200908 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Uridine to 2'-deoxyuridine ratio 7,873 European ancestry individuals NA Affymetrix [15413944] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200909 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Retinol (Vitamin A) to oleoyl-linoleoyl-glycerol (18:1 to 18:2) [2] ratio 7,981 European ancestry individuals NA Affymetrix [15417966] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200910 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan to pyruvate ratio 8,224 European ancestry individuals NA Affymetrix [15430393] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200911 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. tryptophan to tyrosine ratio 8,226 European ancestry individuals NA Affymetrix [15430116] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200912 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to sucrose ratio 7,695 European ancestry individuals NA Affymetrix [15411165] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200913 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Proline to trans-4-hydroxyproline ratio 8,194 European ancestry individuals NA Affymetrix [15427933] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200939 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to EDTA ratio 4,563 European ancestry individuals NA Affymetrix [15443915] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200940 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinate to trans-4-hydroxyproline ratio 8,198 European ancestry individuals NA Affymetrix [15428627] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200941 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate to pyruvate ratio 8,188 European ancestry individuals NA Affymetrix [15428851] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200942 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to EDTA ratio 8,225 European ancestry individuals NA Affymetrix [15430264] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200943 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to pyruvate ratio 8,272 European ancestry individuals NA Affymetrix [15431436] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200944 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to EDTA ratio 8,179 European ancestry individuals NA Affymetrix [15429302] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200945 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate to alanine ratio 8,172 European ancestry individuals NA Affymetrix [15426647] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200946 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to glucose ratio 4,581 European ancestry individuals NA Affymetrix [15444476] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200947 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to mannitol to sorbitol ratio 4,566 European ancestry individuals NA Affymetrix [15443473] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200948 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to N-acetylneuraminate ratio 4,553 European ancestry individuals NA Affymetrix [15443166] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200949 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to mannitol to sorbitol ratio 8,254 European ancestry individuals NA Affymetrix [15430894] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200950 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose to fructose ratio 8,202 European ancestry individuals NA Affymetrix [15428285] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200951 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to cytidine ratio 4,350 European ancestry individuals NA Affymetrix [15431604] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200952 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose-to-mannose ratio 8,191 European ancestry individuals NA Affymetrix [15428816] (imputed) 0 glucose-to-mannose ratio http://www.ebi.ac.uk/efo/EFO_0021404 GCST90200953 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytidine to N-acetylneuraminate ratio 7,683 European ancestry individuals NA Affymetrix [15408615] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200954 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to choline phosphate ratio 4,560 European ancestry individuals NA Affymetrix [15443531] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200955 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cytidine to N-acetylglucosamine to N-acetylgalactosamine ratio 7,427 European ancestry individuals NA Affymetrix [15397897] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200956 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylneuraminate to N-acetylglucosamine to N-acetylgalactosamine ratio 7,988 European ancestry individuals NA Affymetrix [15420526] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200957 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to choline ratio 4,560 European ancestry individuals NA Affymetrix [15443565] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200958 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Choline phosphate to choline ratio 8,196 European ancestry individuals NA Affymetrix [15428652] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200959 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Choline phosphate to phosphoethanolamine ratio 8,213 European ancestry individuals NA Affymetrix [15428585] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200960 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to ornithine ratio 4,566 European ancestry individuals NA Affymetrix [15443986] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200961 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to glutamine ratio 4,569 European ancestry individuals NA Affymetrix [15444140] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200962 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine 5'-monophosphate (IMP) to urate ratio 4,598 European ancestry individuals NA Affymetrix [15456152] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200963 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to 5-oxoproline ratio 4,570 European ancestry individuals NA Affymetrix [15443910] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200964 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamate to 5-oxoproline ratio 8,171 European ancestry individuals NA Affymetrix [15425561] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200965 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) to uridine ratio 4,565 European ancestry individuals NA Affymetrix [15443790] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200966 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to urate ratio 8,204 European ancestry individuals NA Affymetrix [15428926] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200967 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to 5-oxoproline ratio 8,217 European ancestry individuals NA Affymetrix [15430064] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200968 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to N-palmitoyl-sphingosine (d18:1 to 16:0) ratio 8,188 European ancestry individuals NA Affymetrix [15429394] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200969 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to leucine ratio 8,201 European ancestry individuals NA Affymetrix [15429648] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200970 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Leucine to phosphate ratio 8,298 European ancestry individuals NA Affymetrix [15432369] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200971 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Leucine to N-palmitoyl-sphingosine (d18:1 to 16:0) ratio 8,198 European ancestry individuals NA Affymetrix [15429307] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200972 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Proline to glutamate ratio 8,185 European ancestry individuals NA Affymetrix [15428858] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200973 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate to proline ratio 8,241 European ancestry individuals NA Affymetrix [15430856] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200974 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) to caffeine ratio 8,000 European ancestry individuals NA Affymetrix [15422868] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200975 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) to urate ratio 8,181 European ancestry individuals NA Affymetrix [15429221] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200976 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) to paraxanthine ratio 7,776 European ancestry individuals NA Affymetrix [15414535] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200977 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeine to paraxanthine ratio 7,873 European ancestry individuals NA Affymetrix [15418498] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200978 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) to linoleate (18:2n6) ratio 8,162 European ancestry individuals NA Affymetrix [15427706] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200979 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphoethanolamine to choline ratio 8,204 European ancestry individuals NA Affymetrix [15429841] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200980 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeine to linoleate (18:2n6) ratio 7,939 European ancestry individuals NA Affymetrix [15420085] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200981 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Paraxanthine to linoleate (18:2n6) ratio 7,785 European ancestry individuals NA Affymetrix [15415908] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200982 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [1] ratio 7,624 European ancestry individuals NA Affymetrix [15401594] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200983 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol to benzoate ratio 7,387 European ancestry individuals NA Affymetrix [15399344] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200984 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol to oleoyl-linoleoyl-glycerol (18:1 to 18:2) [2] ratio 7,981 European ancestry individuals NA Affymetrix [15418813] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200985 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [2] ratio 7,655 European ancestry individuals NA Affymetrix [15403311] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200986 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Benzoate to oleoyl-linoleoyl-glycerol (18:1 to 18:2) [2] ratio 7,162 European ancestry individuals NA Affymetrix [15385398] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200987 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Benzoate to linoleoyl-arachidonoyl-glycerol (18:2 to 20:4) [1] ratio 6,813 European ancestry individuals NA Affymetrix [15366064] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200988 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyrosine to pyruvate ratio 8,220 European ancestry individuals NA Affymetrix [15429968] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200914 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucose to fructose ratio 8,214 European ancestry individuals NA Affymetrix [15428792] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200915 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructose to sucrose ratio 7,719 European ancestry individuals NA Affymetrix [15412103] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200916 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate to 3-methyl-2-oxobutyrate ratio 8,133 European ancestry individuals NA Affymetrix [15427155] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200917 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphingosine (d18:1 to 16:0) to N-palmitoyl-sphinganine (d18:0 to 16:0) ratio 8,155 European ancestry individuals NA Affymetrix [15426479] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200918 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeine to theophylline ratio 7,756 European ancestry individuals NA Affymetrix [15413178] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200919 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose to glycerol ratio 8,168 European ancestry individuals NA Affymetrix [15429012] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200920 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannose to mannitol to sorbitol ratio 8,208 European ancestry individuals NA Affymetrix [15427587] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200921 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketobutyrate to pyruvate ratio 8,129 European ancestry individuals NA Affymetrix [15427204] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200922 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol to mannitol to sorbitol ratio 8,153 European ancestry individuals NA Affymetrix [15427827] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200923 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-tocopherol to glycerol ratio 8,158 European ancestry individuals NA Affymetrix [15427590] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200924 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeine to theobromine ratio 7,952 European ancestry individuals NA Affymetrix [15419917] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200925 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingosine (d18:1 to 18:0) to N-palmitoyl-sphinganine (d18:0 to 16:0) ratio 8,159 European ancestry individuals NA Affymetrix [15427193] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200926 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theophylline to theobromine ratio 7,858 European ancestry individuals NA Affymetrix [15417883] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200927 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-sphingosine (d18:1 to 16:0) to N-stearoyl-sphingosine (d18:1 to 18:0) ratio 8,191 European ancestry individuals NA Affymetrix [15428318] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200928 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol to carnitine ratio 8,235 European ancestry individuals NA Affymetrix [15430150] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200929 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine to acetylcarnitine (C2) ratio 8,206 European ancestry individuals NA Affymetrix [15429565] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200930 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol to sulfate ratio 8,176 European ancestry individuals NA Affymetrix [15428149] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200931 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol to palmitoylcarnitine (C16) ratio 8,165 European ancestry individuals NA Affymetrix [15428482] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200932 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to proline ratio 8,273 European ancestry individuals NA Affymetrix [15431493] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200933 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetylcarnitine (C2) to propionylcarnitine (C3) ratio 8,200 European ancestry individuals NA Affymetrix [15429545] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200934 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine to propionylcarnitine (C3) ratio 8,185 European ancestry individuals NA Affymetrix [15428940] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200935 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinate to proline ratio 8,209 European ancestry individuals NA Affymetrix [15428539] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200936 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to trans-4-hydroxyproline ratio 8,272 European ancestry individuals NA Affymetrix [15431527] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200937 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-ketoglutarate to alanine ratio 8,272 European ancestry individuals NA Affymetrix [15431458] (imputed) 0 metabolite ratio http://www.ebi.ac.uk/efo/EFO_0022223 GCST90200938 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylanthranilic acid levels 94 South Asian ancestry individuals NA Affymetrix [4460019] (imputed) 0 N-formylanthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0800069 GCST90203407 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenoylcarnitine (C20:3n3 or 6) levels 104 South Asian ancestry individuals NA Affymetrix [4449195] (imputed) 0 dihomo-linolenoylcarnitine (C20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800547 GCST90203586 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (2) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 carotene diol (2) measurement http://www.ebi.ac.uk/efo/EFO_0800171 GCST90203587 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-butenoylglycine levels 84 South Asian ancestry individuals NA Affymetrix [4440161] (imputed) 0 2-butenoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800556 GCST90203588 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linoleoylcarnitine (C20:2) levels 103 South Asian ancestry individuals NA Affymetrix [4466517] (imputed) 0 dihomo-linoleoylcarnitine (C20:2) measurement http://www.ebi.ac.uk/efo/EFO_0800546 GCST90203589 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoylcarnitine (C20:1) levels 106 South Asian ancestry individuals NA Affymetrix [4407804] (imputed) 0 eicosenoylcarnitine (C20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800545 GCST90203590 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyphenylacetoylglutamine levels 57 South Asian ancestry individuals NA Affymetrix [4384777] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203591 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxy-cmpf levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 hydroxy-CMPF measurement http://www.ebi.ac.uk/efo/EFO_0800557 GCST90203592 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyarachidate levels 107 South Asian ancestry individuals NA Affymetrix [4397316] (imputed) 0 2-hydroxyarachidate measurement http://www.ebi.ac.uk/efo/EFO_0800558 GCST90203593 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoleoylcarnitine levels 99 South Asian ancestry individuals NA Affymetrix [4331364] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203594 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecadienedioate (C18:2-DC) levels 107 South Asian ancestry individuals NA Affymetrix [4392648] (imputed) 0 octadecadienedioate (C18:2-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800565 GCST90203595 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecenedioate (C16:1-DC) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 hexadecenedioate (C16:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800562 GCST90203596 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecenedioate (C12:1-DC) levels 106 South Asian ancestry individuals NA Affymetrix [4411431] (imputed) 0 dodecenedioate (C12:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800561 GCST90203597 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) levels 107 South Asian ancestry individuals NA Affymetrix [4392753] (imputed) 0 3-carboxy-4-methyl-5-pentyl-2-furanpropionate (3-CMPFP) measurement http://www.ebi.ac.uk/efo/EFO_0800566 GCST90203598 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioate (C18:1-DC) levels 107 South Asian ancestry individuals NA Affymetrix [4396234] (imputed) 0 octadecenedioate (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800563 GCST90203599 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-2-hexenoylglycine levels 82 South Asian ancestry individuals NA Affymetrix [4486629] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203600 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C12H22O4 (1) levels 76 South Asian ancestry individuals NA Affymetrix [4406091] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203601 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Heptenedioate (C7:1-DC) levels 105 South Asian ancestry individuals NA Affymetrix [4433499] (imputed) 0 heptenedioate (C7:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800564 GCST90203602 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminooctanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N-acetyl-2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800567 GCST90203603 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroxyasparagine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 hydroxyasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800092 GCST90203604 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxybutyroylglycine levels 106 South Asian ancestry individuals NA Affymetrix [4411521] (imputed) 0 3-hydroxybutyroylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800568 GCST90203605 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanoate (PFOA) levels 106 South Asian ancestry individuals NA Affymetrix [4414207] (imputed) 0 perfluorooctanoate (PFOA) measurement http://www.ebi.ac.uk/efo/EFO_0801024 GCST90203606 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glyco-beta-muricholate levels 82 South Asian ancestry individuals NA Affymetrix [4523340] (imputed) 0 glyco-beta-muricholate measurement http://www.ebi.ac.uk/efo/EFO_0800569 GCST90203607 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylhydroxyproline levels 87 South Asian ancestry individuals NA Affymetrix [4387434] (imputed) 0 N-methylhydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800093 GCST90203608 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glucuronide of C10H18O2 (7) levels 66 South Asian ancestry individuals NA Affymetrix [4397468] (imputed) 0 glucuronide of C10H18O2 (7) measurement http://www.ebi.ac.uk/efo/EFO_0800652 GCST90203609 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,n,n-trimethyl-alanylproline betaine (tmap) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N,N,N-trimethyl-alanylproline betaine (TMAP) measurement http://www.ebi.ac.uk/efo/EFO_0800094 GCST90203610 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-oleoylserine levels 101 South Asian ancestry individuals NA Affymetrix [4514174] (imputed) 0 N-oleoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800525 GCST90203561 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/25:0, d19:0/24:1, d20:1/23:0, d19:1/24:0) levels 105 South Asian ancestry individuals NA Affymetrix [4429999] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203562 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/19:0, d19:1/18:0) levels 106 South Asian ancestry individuals NA Affymetrix [4413712] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203563 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) levels 103 South Asian ancestry individuals NA Affymetrix [4458935] (imputed) 0 glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800533 GCST90203564 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nisinate (24:6n3) levels 71 South Asian ancestry individuals NA Affymetrix [4509397] (imputed) 0 nisinate (24:6n3) measurement http://www.ebi.ac.uk/efo/EFO_0800536 GCST90203565 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203566 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/20:0, d16:0/22:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203567 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/21:0, d16:2/23:0) levels 107 South Asian ancestry individuals NA Affymetrix [4392308] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203568 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenoylcarnitine (C18:3) levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 linolenoylcarnitine (C18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800538 GCST90203569 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/14:0, d16:1/16:0) levels 91 South Asian ancestry individuals NA Affymetrix [4500364] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90203570 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidoylcarnitine (C20) levels 98 South Asian ancestry individuals NA Affymetrix [4369671] (imputed) 0 arachidoylcarnitine (C20) measurement http://www.ebi.ac.uk/efo/EFO_0800540 GCST90203571 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroylcarnitine (C24) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 lignoceroylcarnitine (C24) measurement http://www.ebi.ac.uk/efo/EFO_0800541 GCST90203572 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoylcarnitine (C22) levels 100 South Asian ancestry individuals NA Affymetrix [4528225] (imputed) 0 behenoylcarnitine (C22) measurement http://www.ebi.ac.uk/efo/EFO_0800539 GCST90203573 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:1/20:0, d16:1/22:0) levels 107 South Asian ancestry individuals NA Affymetrix [4393321] (imputed) 0 glycosyl ceramide (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800551 GCST90203574 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoylcarnitine (C22:6) levels 81 South Asian ancestry individuals NA Affymetrix [4498439] (imputed) 0 docosahexaenoylcarnitine (C22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800548 GCST90203575 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonoylcarnitine (C20:4) levels 106 South Asian ancestry individuals NA Affymetrix [4412731] (imputed) 0 arachidonoylcarnitine (C20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800544 GCST90203576 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nervonoylcarnitine (C24:1) levels 102 South Asian ancestry individuals NA Affymetrix [4487535] (imputed) 0 nervonoylcarnitine (C24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800549 GCST90203577 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ximenoylcarnitine (C26:1) levels 106 South Asian ancestry individuals NA Affymetrix [4414962] (imputed) 0 ximenoylcarnitine (C26:1) measurement http://www.ebi.ac.uk/efo/EFO_0800543 GCST90203578 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N,N,N-trimethyl-5-aminovalerate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N,N,N-trimethyl-5-aminovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800090 GCST90203579 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortolone glucuronide (1) levels 106 South Asian ancestry individuals NA Affymetrix [4409309] (imputed) 0 cortolone glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800552 GCST90203580 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cerotoylcarnitine (C26) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 cerotoylcarnitine (C26) measurement http://www.ebi.ac.uk/efo/EFO_0800542 GCST90203581 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-furoylcarnitine levels 66 South Asian ancestry individuals NA Affymetrix [4405610] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203582 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-dodecenoylcarnitine (C12:1) levels 97 South Asian ancestry individuals NA Affymetrix [4379629] (imputed) 0 5-dodecenoylcarnitine (C12:1) measurement http://www.ebi.ac.uk/efo/EFO_0800555 GCST90203583 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 carotene diol (1) measurement http://www.ebi.ac.uk/efo/EFO_0800170 GCST90203584 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotene diol (3) levels 99 South Asian ancestry individuals NA Affymetrix [4342513] (imputed) 0 carotene diol (3) measurement http://www.ebi.ac.uk/efo/EFO_0800172 GCST90203585 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylpyruvate levels 59 African ancestry individuals NA Affymetrix [7497538] (imputed) 0 phenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800132 GCST90201755 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aspartate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 aspartate measurement http://www.ebi.ac.uk/efo/EFO_0010462 GCST90201756 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arginine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 arginine measurement http://www.ebi.ac.uk/efo/EFO_0020990 GCST90201757 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(4-hydroxyphenyl)lactate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3- 4-hydroxyphenyl lactate measurement http://www.ebi.ac.uk/efo/EFO_0021008 GCST90201758 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-adenosylhomocysteine (SAH) levels 47 African ancestry individuals NA Affymetrix [7558385] (imputed) 0 S-adenosylhomocysteine measurement http://www.ebi.ac.uk/efo/EFO_0010531 GCST90201759 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90201760 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylmalonate levels 58 African ancestry individuals NA Affymetrix [7586759] (imputed) 0 ethylmalonate measurement http://www.ebi.ac.uk/efo/EFO_0020009 GCST90201761 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylmethionine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-formylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800128 GCST90201762 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-4-hydroxyproline levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90201684 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) levels 31 African ancestry individuals NA Affymetrix [7635207] (imputed) 0 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90201763 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylputrescine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90201764 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-alanine levels 59 African ancestry individuals NA Affymetrix [7496246] (imputed) 0 beta-alanine measurement http://www.ebi.ac.uk/efo/EFO_0800640 GCST90201765 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 3',5'-cyclic monophosphate (camp) levels 51 African ancestry individuals NA Affymetrix [7758329] (imputed) 0 cyclic adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010473 GCST90201766 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 cystine measurement http://www.ebi.ac.uk/efo/EFO_0800134 GCST90201767 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 gamma-glutamylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0021137 GCST90201768 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cystathionine levels 57 African ancestry individuals NA Affymetrix [7522483] (imputed) 0 cystathionine measurement http://www.ebi.ac.uk/efo/EFO_0010474 GCST90201769 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphinganine levels 51 African ancestry individuals NA Affymetrix [7768518] (imputed) 0 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90201770 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholate levels 56 African ancestry individuals NA Affymetrix [7571727] (imputed) 0 deoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010475 GCST90201771 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Biliverdin levels 59 African ancestry individuals NA Affymetrix [7499281] (imputed) 0 biliverdin measurement http://www.ebi.ac.uk/efo/EFO_0021033 GCST90201772 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarate (C5-DC) levels 56 African ancestry individuals NA Affymetrix [7566662] (imputed) 0 glutarate (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800620 GCST90201773 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine levels 58 African ancestry individuals NA Affymetrix [7511543] (imputed) 0 sphingosine measurement http://www.ebi.ac.uk/efo/EFO_0800618 GCST90201774 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholesterol levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 total cholesterol measurement http://www.ebi.ac.uk/efo/EFO_0004574 GCST90201775 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphocholine levels 59 African ancestry individuals NA Affymetrix [7498120] (imputed) 0 choline phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800617 GCST90201776 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatinine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 creatinine measurement http://www.ebi.ac.uk/efo/EFO_0004518 GCST90201777 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycine levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 glycine measurement http://www.ebi.ac.uk/efo/EFO_0009767 GCST90201778 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21339 levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 X-21339 measurement http://www.ebi.ac.uk/efo/EFO_0800808 GCST90201975 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21607 levels 59 African ancestry individuals NA Affymetrix [7569028] (imputed) 0 X-21607 measurement http://www.ebi.ac.uk/efo/EFO_0800819 GCST90201976 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21319 levels 58 African ancestry individuals NA Affymetrix [7516462] (imputed) 0 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90201977 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21353 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-21353 measurement http://www.ebi.ac.uk/efo/EFO_0800809 GCST90201978 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21364 levels 59 African ancestry individuals NA Affymetrix [7495100] (imputed) 0 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90201979 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21470 levels 57 African ancestry individuals NA Affymetrix [7552324] (imputed) 0 X-21470 measurement http://www.ebi.ac.uk/efo/EFO_0800817 GCST90201980 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21821 levels 56 African ancestry individuals NA Affymetrix [7559651] (imputed) 0 X-21821 measurement http://www.ebi.ac.uk/efo/EFO_0800829 GCST90201981 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21733 levels 52 African ancestry individuals NA Affymetrix [7683513] (imputed) 0 X-21733 measurement http://www.ebi.ac.uk/efo/EFO_0800820 GCST90201982 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21467 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90201983 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21834 levels 52 African ancestry individuals NA Affymetrix [7774987] (imputed) 0 X-21834 measurement http://www.ebi.ac.uk/efo/EFO_0800833 GCST90201984 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21736 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-21736 measurement http://www.ebi.ac.uk/efo/EFO_0800821 GCST90201985 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23655 levels 39 African ancestry individuals NA Affymetrix [7069918] (imputed) 0 X-23655 measurement http://www.ebi.ac.uk/efo/EFO_0800856 GCST90201986 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23680 levels 59 African ancestry individuals NA Affymetrix [7489047] (imputed) 0 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90201987 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23587 levels 56 African ancestry individuals NA Affymetrix [7689236] (imputed) 0 X-23587 measurement http://www.ebi.ac.uk/efo/EFO_0800849 GCST90201988 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetylglutamine levels 102 South Asian ancestry individuals NA Affymetrix [4490116] (imputed) 0 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90203550 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800483 GCST90203551 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/17:0, d17:1/18:0) levels 69 South Asian ancestry individuals NA Affymetrix [4275497] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90203552 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosatrienoate (22:3n6) levels 56 South Asian ancestry individuals NA Affymetrix [4337947] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203553 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) levels 107 South Asian ancestry individuals NA Affymetrix [4393321] (imputed) 0 glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800520 GCST90203554 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-tricosanoyl-sphingadienine (d18:2/23:0) levels 78 South Asian ancestry individuals NA Affymetrix [4324360] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90203555 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-heptadecasphingosine (d17:1/16:0) levels 87 South Asian ancestry individuals NA Affymetrix [4385097] (imputed) 0 N-palmitoyl-heptadecasphingosine (d17:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800531 GCST90203556 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcholine levels 83 South Asian ancestry individuals NA Affymetrix [4465747] (imputed) 0 stearoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800534 GCST90203557 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:2/24:1, d18:1/24:2) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 glycosyl ceramide (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0800532 GCST90203558 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:2/16:0, d18:2/15:0) levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90203559 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoylcholine levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 linoleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800535 GCST90203560 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gluconate levels 58 African ancestry individuals NA Affymetrix [7523840] (imputed) 0 gluconate measurement http://www.ebi.ac.uk/efo/EFO_0801064 GCST90201779 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cortisone levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 cortisone measurement http://www.ebi.ac.uk/efo/EFO_0021118 GCST90201780 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-Hydroxybutyrate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 3-hydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010982 GCST90201781 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteinylglycine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 cysteinylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800133 GCST90201782 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Flavin adenine dinucleotide (FAD) levels 48 African ancestry individuals NA Affymetrix [7477946] (imputed) 0 flavin adenine dinucleotide (FAD) measurement http://www.ebi.ac.uk/efo/EFO_0800177 GCST90201783 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinate levels 59 African ancestry individuals NA Affymetrix [7496282] (imputed) 0 succinate measurement http://www.ebi.ac.uk/efo/EFO_0011002 GCST90201784 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycocholate measurement http://www.ebi.ac.uk/efo/EFO_0010491 GCST90201785 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guanidinoacetate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 guanidinoacetate measurement http://www.ebi.ac.uk/efo/EFO_0800135 GCST90201786 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lysine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90201787 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Malate levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 malate measurement http://www.ebi.ac.uk/efo/EFO_0010508 GCST90201788 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylalanine levels 59 African ancestry individuals NA Affymetrix [7495043] (imputed) 0 phenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0005001 GCST90201789 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphate levels (UKB data field 30810) 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010968 GCST90201790 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 histidine measurement http://www.ebi.ac.uk/efo/EFO_0009769 GCST90201791 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ornithine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 ornithine measurement http://www.ebi.ac.uk/efo/EFO_0009776 GCST90201792 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearate (18:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 stearate 18:0 measurement http://www.ebi.ac.uk/efo/EFO_0021074 GCST90201793 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Orotate levels 58 African ancestry individuals NA Affymetrix [7542064] (imputed) 0 orotate measurement http://www.ebi.ac.uk/efo/EFO_0800642 GCST90201794 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoleate (16:1n7) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 palmitoleate 16:1n7 measurement http://www.ebi.ac.uk/efo/EFO_0021072 GCST90201795 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Inosine levels 37 African ancestry individuals NA Affymetrix [7384022] (imputed) 0 inosine measurement http://www.ebi.ac.uk/efo/EFO_0010503 GCST90201796 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12026 levels 59 African ancestry individuals NA Affymetrix [7498120] (imputed) 0 X-12026 measurement http://www.ebi.ac.uk/efo/EFO_0800700 GCST90201868 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12100 levels 59 African ancestry individuals NA Affymetrix [7497274] (imputed) 0 X-12100 measurement http://www.ebi.ac.uk/efo/EFO_0800701 GCST90201869 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12101 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-12101 measurement http://www.ebi.ac.uk/efo/EFO_0800702 GCST90201870 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11852 levels 55 African ancestry individuals NA Affymetrix [7589235] (imputed) 0 X-11852 measurement http://www.ebi.ac.uk/efo/EFO_0021271 GCST90201871 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12007 levels 57 African ancestry individuals NA Affymetrix [7543617] (imputed) 0 X-12007 measurement http://www.ebi.ac.uk/efo/EFO_0021276 GCST90201872 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12104 levels 50 African ancestry individuals NA Affymetrix [7433541] (imputed) 0 X-12104 measurement http://www.ebi.ac.uk/efo/EFO_0800703 GCST90201873 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11850 levels 51 African ancestry individuals NA Affymetrix [7736277] (imputed) 0 X-11850 measurement http://www.ebi.ac.uk/efo/EFO_0021270 GCST90201874 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21310 levels 57 African ancestry individuals NA Affymetrix [7555831] (imputed) 0 X-21310 measurement http://www.ebi.ac.uk/efo/EFO_0800805 GCST90201950 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17685 levels 41 African ancestry individuals NA Affymetrix [7834351] (imputed) 0 X-17685 measurement http://www.ebi.ac.uk/efo/EFO_0800786 GCST90201951 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17438 levels 50 African ancestry individuals NA Affymetrix [7478020] (imputed) 0 X-17438 measurement http://www.ebi.ac.uk/efo/EFO_0800781 GCST90201952 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17653 levels 58 African ancestry individuals NA Affymetrix [7574407] (imputed) 0 X-17653 measurement http://www.ebi.ac.uk/efo/EFO_0800783 GCST90201953 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17654 levels 57 African ancestry individuals NA Affymetrix [7539364] (imputed) 0 X-17654 measurement http://www.ebi.ac.uk/efo/EFO_0800784 GCST90201954 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18779 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201955 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17676 levels 58 African ancestry individuals NA Affymetrix [7515709] (imputed) 0 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90201956 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18886 levels 59 African ancestry individuals NA Affymetrix [7486932] (imputed) 0 X-18886 measurement http://www.ebi.ac.uk/efo/EFO_0800790 GCST90201957 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21286 levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 X-21286 measurement http://www.ebi.ac.uk/efo/EFO_0800804 GCST90201958 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18345 levels 44 African ancestry individuals NA Affymetrix [7701285] (imputed) 0 X-18345 measurement http://www.ebi.ac.uk/efo/EFO_0800789 GCST90201959 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17690 levels 48 African ancestry individuals NA Affymetrix [7649372] (imputed) 0 X-17690 measurement http://www.ebi.ac.uk/efo/EFO_0800788 GCST90201960 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19141 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-19141 measurement http://www.ebi.ac.uk/efo/EFO_0800799 GCST90201961 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18913 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-18913 measurement http://www.ebi.ac.uk/efo/EFO_0800795 GCST90201962 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19438 levels 54 African ancestry individuals NA Affymetrix [7646975] (imputed) 0 X-19438 measurement http://www.ebi.ac.uk/efo/EFO_0800801 GCST90201963 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19299 levels 47 African ancestry individuals NA Affymetrix [7579154] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201964 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18887 levels 53 African ancestry individuals NA Affymetrix [7713231] (imputed) 0 X-18887 measurement http://www.ebi.ac.uk/efo/EFO_0800791 GCST90201965 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21807 levels 34 African ancestry individuals NA Affymetrix [7521598] (imputed) 0 X-21807 measurement http://www.ebi.ac.uk/efo/EFO_0800827 GCST90201966 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21441 levels 57 African ancestry individuals NA Affymetrix [7555363] (imputed) 0 X-21441 measurement http://www.ebi.ac.uk/efo/EFO_0800814 GCST90201967 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21796 levels 59 African ancestry individuals NA Affymetrix [7486932] (imputed) 0 X-21796 measurement http://www.ebi.ac.uk/efo/EFO_0800825 GCST90201968 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21752 levels 40 African ancestry individuals NA Affymetrix [7733326] (imputed) 0 X-21752 measurement http://www.ebi.ac.uk/efo/EFO_0800824 GCST90201969 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21383 levels 59 African ancestry individuals NA Affymetrix [7500538] (imputed) 0 X-21383 measurement http://www.ebi.ac.uk/efo/EFO_0800812 GCST90201970 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21829 levels 59 African ancestry individuals NA Affymetrix [7496246] (imputed) 0 X-21829 measurement http://www.ebi.ac.uk/efo/EFO_0800830 GCST90201971 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21442 levels 40 African ancestry individuals NA Affymetrix [7327920] (imputed) 0 X-21442 measurement http://www.ebi.ac.uk/efo/EFO_0800815 GCST90201972 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21355 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-21355 measurement http://www.ebi.ac.uk/efo/EFO_0800810 GCST90201973 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21471 levels 59 African ancestry individuals NA Affymetrix [7546954] (imputed) 0 X-21471 measurement http://www.ebi.ac.uk/efo/EFO_0800818 GCST90201974 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13507 levels 57 African ancestry individuals NA Affymetrix [7596900] (imputed) 0 X-13507 measurement http://www.ebi.ac.uk/efo/EFO_0800736 GCST90201925 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17346 levels 45 African ancestry individuals NA Affymetrix [7529463] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201926 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16580 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90201927 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17351 levels 55 African ancestry individuals NA Affymetrix [7590958] (imputed) 0 X-17351 measurement http://www.ebi.ac.uk/efo/EFO_0800774 GCST90201928 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17010 levels 59 African ancestry individuals NA Affymetrix [7496533] (imputed) 0 X-17010 measurement http://www.ebi.ac.uk/efo/EFO_0800767 GCST90201929 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17367 levels 42 African ancestry individuals NA Affymetrix [7730511] (imputed) 0 X-17367 measurement http://www.ebi.ac.uk/efo/EFO_0800779 GCST90201930 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17328 levels 44 African ancestry individuals NA Affymetrix [7770104] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201931 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16935 levels 57 African ancestry individuals NA Affymetrix [7605781] (imputed) 0 X-16935 measurement http://www.ebi.ac.uk/efo/EFO_0800763 GCST90201932 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17146 levels 57 African ancestry individuals NA Affymetrix [7539140] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201933 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15503 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-15503 measurement http://www.ebi.ac.uk/efo/EFO_0800753 GCST90201934 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16124 levels 36 African ancestry individuals NA Affymetrix [7498302] (imputed) 0 X-16124 measurement http://www.ebi.ac.uk/efo/EFO_0800757 GCST90201935 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17354 levels 32 African ancestry individuals NA Affymetrix [7488896] (imputed) 0 X-17354 measurement http://www.ebi.ac.uk/efo/EFO_0800776 GCST90201936 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16087 levels 46 African ancestry individuals NA Affymetrix [7598249] (imputed) 0 X-16087 measurement http://www.ebi.ac.uk/efo/EFO_0800756 GCST90201937 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15486 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90201938 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15461 levels 59 African ancestry individuals NA Affymetrix [7496750] (imputed) 0 X-15461 measurement http://www.ebi.ac.uk/efo/EFO_0800749 GCST90201939 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15728 levels 56 African ancestry individuals NA Affymetrix [7590726] (imputed) 0 X-15728 measurement http://www.ebi.ac.uk/efo/EFO_0020024 GCST90201940 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16964 levels 58 African ancestry individuals NA Affymetrix [7573837] (imputed) 0 X-16964 measurement http://www.ebi.ac.uk/efo/EFO_0020011 GCST90201941 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17325 levels 51 African ancestry individuals NA Affymetrix [7721342] (imputed) 0 X-17325 measurement http://www.ebi.ac.uk/efo/EFO_0800771 GCST90201942 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15523 levels 57 African ancestry individuals NA Affymetrix [7544096] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201943 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17335 levels 51 African ancestry individuals NA Affymetrix [7878050] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90201944 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16397 levels 56 African ancestry individuals NA Affymetrix [7712130] (imputed) 0 X-16397 measurement http://www.ebi.ac.uk/efo/EFO_0800758 GCST90201945 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18888 levels 47 African ancestry individuals NA Affymetrix [7545221] (imputed) 0 X-18888 measurement http://www.ebi.ac.uk/efo/EFO_0800792 GCST90201946 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18921 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-18921 measurement http://www.ebi.ac.uk/efo/EFO_0800796 GCST90201947 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18922 levels 59 African ancestry individuals NA Affymetrix [7497242] (imputed) 0 X-18922 measurement http://www.ebi.ac.uk/efo/EFO_0800797 GCST90201948 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18901 levels 59 African ancestry individuals NA Affymetrix [7497242] (imputed) 0 X-18901 measurement http://www.ebi.ac.uk/efo/EFO_0800794 GCST90201949 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12013 levels 50 African ancestry individuals NA Affymetrix [7711108] (imputed) 0 X-12013 measurement http://www.ebi.ac.uk/efo/EFO_0021277 GCST90201875 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11858 levels 36 African ancestry individuals NA Affymetrix [7515317] (imputed) 0 X-11858 measurement http://www.ebi.ac.uk/efo/EFO_0021272 GCST90201876 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11880 levels 58 African ancestry individuals NA Affymetrix [7588729] (imputed) 0 X-11880 measurement http://www.ebi.ac.uk/efo/EFO_0800698 GCST90201877 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11847 levels 46 African ancestry individuals NA Affymetrix [7542415] (imputed) 0 X-11847 measurement http://www.ebi.ac.uk/efo/EFO_0021268 GCST90201878 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12216 levels 58 African ancestry individuals NA Affymetrix [7527374] (imputed) 0 X-12216 measurement http://www.ebi.ac.uk/efo/EFO_0021294 GCST90201879 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11843 levels 52 African ancestry individuals NA Affymetrix [7720118] (imputed) 0 X-11843 measurement http://www.ebi.ac.uk/efo/EFO_0021266 GCST90201880 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12117 levels 49 African ancestry individuals NA Affymetrix [7421847] (imputed) 0 X-12117 measurement http://www.ebi.ac.uk/efo/EFO_0800706 GCST90201881 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12112 levels 56 African ancestry individuals NA Affymetrix [7566849] (imputed) 0 X-12112 measurement http://www.ebi.ac.uk/efo/EFO_0800705 GCST90201882 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11795 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-11795 measurement http://www.ebi.ac.uk/efo/EFO_0021261 GCST90201883 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-11849 levels 43 African ancestry individuals NA Affymetrix [7667463] (imputed) 0 X-11849 measurement http://www.ebi.ac.uk/efo/EFO_0021269 GCST90201884 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12193 levels 55 African ancestry individuals NA Affymetrix [7588413] (imputed) 0 X-12193 measurement http://www.ebi.ac.uk/efo/EFO_0800710 GCST90201885 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12261 levels 37 African ancestry individuals NA Affymetrix [7371811] (imputed) 0 X-12261 measurement http://www.ebi.ac.uk/efo/EFO_0021301 GCST90201886 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12462 levels 59 African ancestry individuals NA Affymetrix [7488161] (imputed) 0 X-12462 measurement http://www.ebi.ac.uk/efo/EFO_0800717 GCST90201887 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12410 levels 57 African ancestry individuals NA Affymetrix [7618838] (imputed) 0 X-12410 measurement http://www.ebi.ac.uk/efo/EFO_0800715 GCST90201888 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12221 levels 48 African ancestry individuals NA Affymetrix [7471846] (imputed) 0 X-12221 measurement http://www.ebi.ac.uk/efo/EFO_0800711 GCST90201889 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12407 levels 50 African ancestry individuals NA Affymetrix [7469160] (imputed) 0 X-12407 measurement http://www.ebi.ac.uk/efo/EFO_0021304 GCST90201890 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12306 levels 47 African ancestry individuals NA Affymetrix [7542258] (imputed) 0 X-12306 measurement http://www.ebi.ac.uk/efo/EFO_0800714 GCST90201891 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12730 levels 50 African ancestry individuals NA Affymetrix [7758837] (imputed) 0 X-12730 measurement http://www.ebi.ac.uk/efo/EFO_0800724 GCST90201892 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12812 levels 49 African ancestry individuals NA Affymetrix [7587455] (imputed) 0 X-12812 measurement http://www.ebi.ac.uk/efo/EFO_0800728 GCST90201893 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12818 levels 42 African ancestry individuals NA Affymetrix [7623316] (imputed) 0 X-12818 measurement http://www.ebi.ac.uk/efo/EFO_0800729 GCST90201894 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12544 levels 54 African ancestry individuals NA Affymetrix [7669592] (imputed) 0 X-12544 measurement http://www.ebi.ac.uk/efo/EFO_0021315 GCST90201895 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12731 levels 37 African ancestry individuals NA Affymetrix [7422788] (imputed) 0 X-12731 measurement http://www.ebi.ac.uk/efo/EFO_0800725 GCST90201896 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12283 levels 56 African ancestry individuals NA Affymetrix [7559560] (imputed) 0 X-12283 measurement http://www.ebi.ac.uk/efo/EFO_0800713 GCST90201897 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12701 levels 41 African ancestry individuals NA Affymetrix [7652242] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201898 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12714 levels 47 African ancestry individuals NA Affymetrix [7538745] (imputed) 0 X-12714 measurement http://www.ebi.ac.uk/efo/EFO_0800722 GCST90201899 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12729 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-12729 measurement http://www.ebi.ac.uk/efo/EFO_0021328 GCST90201900 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12798 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-12798 measurement http://www.ebi.ac.uk/efo/EFO_0021335 GCST90201901 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12680 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-12680 measurement http://www.ebi.ac.uk/efo/EFO_0021320 GCST90201902 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12740 levels 46 African ancestry individuals NA Affymetrix [7663778] (imputed) 0 X-12740 measurement http://www.ebi.ac.uk/efo/EFO_0021330 GCST90201903 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12707 levels 55 African ancestry individuals NA Affymetrix [7682674] (imputed) 0 X-12707 measurement http://www.ebi.ac.uk/efo/EFO_0800720 GCST90201904 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12411 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-12411 measurement http://www.ebi.ac.uk/efo/EFO_0800716 GCST90201905 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12849 levels 58 African ancestry individuals NA Affymetrix [7517597] (imputed) 0 X-12849 measurement http://www.ebi.ac.uk/efo/EFO_0800732 GCST90201906 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12851 levels 53 African ancestry individuals NA Affymetrix [7649232] (imputed) 0 X-12851 measurement http://www.ebi.ac.uk/efo/EFO_0021342 GCST90201907 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13553 levels 59 African ancestry individuals NA Affymetrix [7496533] (imputed) 0 X-13553 measurement http://www.ebi.ac.uk/efo/EFO_0021355 GCST90201908 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13684 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-13684 measurement http://www.ebi.ac.uk/efo/EFO_0800737 GCST90201909 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13723 levels 33 African ancestry individuals NA Affymetrix [7809816] (imputed) 0 X-13723 measurement http://www.ebi.ac.uk/efo/EFO_0800739 GCST90201910 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-14056 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-14056 measurement http://www.ebi.ac.uk/efo/EFO_0021361 GCST90201911 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13844 levels 51 African ancestry individuals NA Affymetrix [7688773] (imputed) 0 X-13844 measurement http://www.ebi.ac.uk/efo/EFO_0800744 GCST90201912 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13866 levels 59 African ancestry individuals NA Affymetrix [7497538] (imputed) 0 X-13866 measurement http://www.ebi.ac.uk/efo/EFO_0800745 GCST90201913 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-14939 levels 59 African ancestry individuals NA Affymetrix [7500737] (imputed) 0 X-14939 measurement http://www.ebi.ac.uk/efo/EFO_0800747 GCST90201914 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12906 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-12906 measurement http://www.ebi.ac.uk/efo/EFO_0800733 GCST90201915 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13729 levels 55 African ancestry individuals NA Affymetrix [7619388] (imputed) 0 X-13729 measurement http://www.ebi.ac.uk/efo/EFO_0800742 GCST90201916 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12830 levels 37 African ancestry individuals NA Affymetrix [7267910] (imputed) 0 X-12830 measurement http://www.ebi.ac.uk/efo/EFO_0021337 GCST90201917 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12839 levels 31 African ancestry individuals NA Affymetrix [7612197] (imputed) 0 X-12839 measurement http://www.ebi.ac.uk/efo/EFO_0800731 GCST90201918 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12844 levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 X-12844 measurement http://www.ebi.ac.uk/efo/EFO_0021339 GCST90201919 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13431 levels 58 African ancestry individuals NA Affymetrix [7491571] (imputed) 0 X-13431 measurement http://www.ebi.ac.uk/efo/EFO_0800735 GCST90201920 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12847 levels 57 African ancestry individuals NA Affymetrix [7608504] (imputed) 0 X-12847 measurement http://www.ebi.ac.uk/efo/EFO_0021340 GCST90201921 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13695 levels 46 African ancestry individuals NA Affymetrix [7645194] (imputed) 0 X-13695 measurement http://www.ebi.ac.uk/efo/EFO_0800738 GCST90201922 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-13007 levels 51 African ancestry individuals NA Affymetrix [7792887] (imputed) 0 X-13007 measurement http://www.ebi.ac.uk/efo/EFO_0800734 GCST90201923 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-12822 levels 57 African ancestry individuals NA Affymetrix [7602656] (imputed) 0 X-12822 measurement http://www.ebi.ac.uk/efo/EFO_0800730 GCST90201924 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Kynurenine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 kynurenine measurement http://www.ebi.ac.uk/efo/EFO_0008529 GCST90203108 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol 3-phosphate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 glycerol-3-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0010488 GCST90203109 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hippurate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 hippurate measurement http://www.ebi.ac.uk/efo/EFO_0010992 GCST90203110 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phenylpropionate hydrocinnamate levels 91 South Asian ancestry individuals NA Affymetrix [4516699] (imputed) 0 3-phenylpropionate hydrocinnamate measurement http://www.ebi.ac.uk/efo/EFO_0021010 GCST90203111 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglutamate levels 100 South Asian ancestry individuals NA Affymetrix [4522823] (imputed) 0 N-acetylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800005 GCST90203112 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Xanthurenate levels 101 South Asian ancestry individuals NA Affymetrix [4508875] (imputed) 0 xanthurenate measurement http://www.ebi.ac.uk/efo/EFO_0010551 GCST90203113 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxovalerate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-methyl-2-oxovalerate measurement http://www.ebi.ac.uk/efo/EFO_0021021 GCST90203114 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 quinate measurement http://www.ebi.ac.uk/efo/EFO_0021167 GCST90203115 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingosine 1-phosphate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 sphingosine 1-phosphate measurement http://www.ebi.ac.uk/efo/EFO_0800185 GCST90203116 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theobromine levels 104 South Asian ancestry individuals NA Affymetrix [4454126] (imputed) 0 theobromine measurement http://www.ebi.ac.uk/efo/EFO_0021179 GCST90203117 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPI (18:0) levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 1-stearoyl-GPI (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800188 GCST90203118 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dipalmitoyl-gpc (16:0/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1,2-dipalmitoyl-GPC (16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800189 GCST90203119 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,5-anhydroglucitol (1,5-ag) levels 105 South Asian ancestry individuals NA Affymetrix [4436272] (imputed) 0 1,5 anhydroglucitol measurement http://www.ebi.ac.uk/efo/EFO_0008009 GCST90203120 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) levels 105 South Asian ancestry individuals NA Affymetrix [4429999] (imputed) 0 1-stearoyl-2-arachidonoyl-GPI (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800184 GCST90203121 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxyisocaproate levels 107 South Asian ancestry individuals NA Affymetrix [4390292] (imputed) 0 alpha-hydroxyisocaproate measurement http://www.ebi.ac.uk/efo/EFO_0800009 GCST90203122 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maleate levels 106 South Asian ancestry individuals NA Affymetrix [4411781] (imputed) 0 maleate measurement http://www.ebi.ac.uk/efo/EFO_0010509 GCST90203123 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPS (18:0/18:1) levels 104 South Asian ancestry individuals NA Affymetrix [4448319] (imputed) 0 1-stearoyl-2-oleoyl-GPS (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800187 GCST90203124 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolelactate levels 107 South Asian ancestry individuals NA Affymetrix [4390292] (imputed) 0 indolelactate measurement http://www.ebi.ac.uk/efo/EFO_0020012 GCST90203125 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoate DHA; 22:6n3 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 docosahexaenoate DHA; 22:6n3 measurement http://www.ebi.ac.uk/efo/EFO_0021047 GCST90203126 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-palmitoyl-gpc (14:0/16:0) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-myristoyl-2-palmitoyl-GPC (14:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800191 GCST90203127 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerate (i5:0) levels 103 South Asian ancestry individuals NA Affymetrix [4479939] (imputed) 0 isovalerate (i5:0) measurement http://www.ebi.ac.uk/efo/EFO_0800010 GCST90203128 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-indoxyl sulfate levels 107 South Asian ancestry individuals NA Affymetrix [4391933] (imputed) 0 indoxyl sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010502 GCST90203129 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetylphenol sulfate levels 92 South Asian ancestry individuals NA Affymetrix [4498630] (imputed) 0 4-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800942 GCST90203130 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800193 GCST90203131 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gentisate levels 105 South Asian ancestry individuals NA Affymetrix [4429175] (imputed) 0 gentisate measurement http://www.ebi.ac.uk/efo/EFO_0800007 GCST90203132 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyoctanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 2-hydroxyoctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800192 GCST90203133 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methyl-2-oxopentanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 4-methyl-2-oxopentanoate measurement http://www.ebi.ac.uk/efo/EFO_0021022 GCST90203134 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenyllactate (PLA) levels in elite athletes 106 South Asian ancestry individuals NA Affymetrix [4408014] (imputed) 0 Phenyllactate (PLA) measurement http://www.ebi.ac.uk/efo/EFO_0021662 GCST90203135 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylcarnitine levels (Biocrates platform) 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 hexanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021040 GCST90203136 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetylcarnitine levels (Biocrates platform) 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 acetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021038 GCST90203137 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine s-sulfate levels 106 South Asian ancestry individuals NA Affymetrix [4406238] (imputed) 0 cysteine s-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800013 GCST90203138 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartronate (hydroxymalonate) levels 106 South Asian ancestry individuals NA Affymetrix [4412969] (imputed) 0 tartronate (hydroxymalonate) measurement http://www.ebi.ac.uk/efo/EFO_0800944 GCST90203139 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxypyridine levels 65 South Asian ancestry individuals NA Affymetrix [4415999] (imputed) 0 blood 2,3-dihydroxypyridine measurement http://www.ebi.ac.uk/efo/EFO_0022199 GCST90203140 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcarnitine levels (Metabolon platform) 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 palmitoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021044 GCST90203141 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oxalate (ethanedioate) levels 107 South Asian ancestry individuals NA Affymetrix [4390596] (imputed) 0 oxalate measurement http://www.ebi.ac.uk/efo/EFO_0010517 GCST90203142 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-linoleoylglycerol (18:2) levels 86 South Asian ancestry individuals NA Affymetrix [4391072] (imputed) 0 2-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800197 GCST90203143 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800198 GCST90203144 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoylglycerol (18:1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-oleoylglycerol (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800195 GCST90203145 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl-2-oxobutyrate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-methyl-2-oxobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0021020 GCST90203146 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythritol levels in elite athletes 106 South Asian ancestry individuals NA Affymetrix [4413642] (imputed) 0 erythritol measurement http://www.ebi.ac.uk/efo/EFO_0021171 GCST90203147 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homocitrulline levels 101 South Asian ancestry individuals NA Affymetrix [4511518] (imputed) 0 homocitrulline measurement http://www.ebi.ac.uk/efo/EFO_0021018 GCST90203148 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citramalate levels 83 South Asian ancestry individuals NA Affymetrix [4475773] (imputed) 0 blood citramalate measurement http://www.ebi.ac.uk/efo/EFO_0022198 GCST90203149 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. EDTA levels 107 South Asian ancestry individuals NA Affymetrix [4392976] (imputed) 0 EDTA measurement http://www.ebi.ac.uk/efo/EFO_0800946 GCST90203150 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Iminodiacetate (IDA) levels 106 South Asian ancestry individuals NA Affymetrix [4405669] (imputed) 0 iminodiacetate (IDA) measurement http://www.ebi.ac.uk/efo/EFO_0800945 GCST90203151 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxymyristate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 blood 3-hydroxymyristate measurement http://www.ebi.ac.uk/efo/EFO_0022197 GCST90203152 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Threonate levels 106 South Asian ancestry individuals NA Affymetrix [4405876] (imputed) 0 threonate measurement http://www.ebi.ac.uk/efo/EFO_0021032 GCST90203153 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglycine levels 106 South Asian ancestry individuals NA Affymetrix [4412675] (imputed) 0 N-acetylglycine measurement http://www.ebi.ac.uk/efo/EFO_0021002 GCST90203154 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trigonelline levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 trigonelline (N'-methylnicotinate) measurement http://www.ebi.ac.uk/efo/EFO_0800154 GCST90203155 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate levels 76 South Asian ancestry individuals NA Affymetrix [4392694] (imputed) 0 glycolithocholate measurement http://www.ebi.ac.uk/efo/EFO_0800203 GCST90203156 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Galactonate levels 97 South Asian ancestry individuals NA Affymetrix [4373292] (imputed) 0 galactonate measurement http://www.ebi.ac.uk/efo/EFO_0800145 GCST90203157 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylhistidine levels 107 South Asian ancestry individuals NA Affymetrix [4393856] (imputed) 0 1-Methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021543 GCST90203158 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dodecanedioate levels 106 South Asian ancestry individuals NA Affymetrix [4410525] (imputed) 0 dodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021054 GCST90203159 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltyrosine levels 98 South Asian ancestry individuals NA Affymetrix [4365741] (imputed) 0 N-acetyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0020021 GCST90203160 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrylglycine levels 69 South Asian ancestry individuals NA Affymetrix [4347961] (imputed) 0 butyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800208 GCST90203161 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyhexanoate levels 89 South Asian ancestry individuals NA Affymetrix [4346637] (imputed) 0 5-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800206 GCST90203162 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetate levels 106 South Asian ancestry individuals NA Affymetrix [4404195] (imputed) 0 indoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0021015 GCST90203163 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C4 levels 104 South Asian ancestry individuals NA Affymetrix [4449257] (imputed) 0 butyrylcarnitine (C4) measurement http://www.ebi.ac.uk/efo/EFO_0800201 GCST90203164 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyridoxate levels 106 South Asian ancestry individuals NA Affymetrix [4415427] (imputed) 0 pyridoxate measurement http://www.ebi.ac.uk/efo/EFO_0010527 GCST90203165 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoylglycerol (18:2) levels 107 South Asian ancestry individuals NA Affymetrix [4393796] (imputed) 0 1-linoleoylglycerol (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800199 GCST90203166 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolepropionate levels 101 South Asian ancestry individuals NA Affymetrix [4522823] (imputed) 0 indolepropionate measurement http://www.ebi.ac.uk/efo/EFO_0021016 GCST90203167 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxysebacate levels 91 South Asian ancestry individuals NA Affymetrix [4513191] (imputed) 0 3-hydroxysebacate measurement http://www.ebi.ac.uk/efo/EFO_0800205 GCST90203168 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3-dimethylurate levels 96 South Asian ancestry individuals NA Affymetrix [4410424] (imputed) 0 1,3-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800948 GCST90203169 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylcarnitine (c4) levels 107 South Asian ancestry individuals NA Affymetrix [4390659] (imputed) 0 isobutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021023 GCST90203170 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxylaurate levels 106 South Asian ancestry individuals NA Affymetrix [4416483] (imputed) 0 3-hydroxylaurate measurement http://www.ebi.ac.uk/efo/EFO_0800204 GCST90203171 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylxanthine levels 100 South Asian ancestry individuals NA Affymetrix [4522031] (imputed) 0 3-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021175 GCST90203172 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylvaline levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 gamma-glutamylvaline measurement http://www.ebi.ac.uk/efo/EFO_0021145 GCST90203173 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylglycine levels 81 South Asian ancestry individuals NA Affymetrix [4525057] (imputed) 0 propionylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800207 GCST90203174 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propionylcarnitine (c3) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 propionylcarnitine (C3) measurement http://www.ebi.ac.uk/efo/EFO_0800210 GCST90203175 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24546 levels 91 South Asian ancestry individuals NA Affymetrix [4534815] (imputed) 0 X-24546 measurement http://www.ebi.ac.uk/efo/EFO_0800893 GCST90204037 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24736 levels 70 South Asian ancestry individuals NA Affymetrix [4589845] (imputed) 0 X-24736 measurement http://www.ebi.ac.uk/efo/EFO_0800904 GCST90204038 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24565 levels 56 South Asian ancestry individuals NA Affymetrix [4366508] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204039 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24585 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204040 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24588 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-24588 measurement http://www.ebi.ac.uk/efo/EFO_0800898 GCST90204041 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24518 levels 81 South Asian ancestry individuals NA Affymetrix [4554091] (imputed) 0 X-24518 measurement http://www.ebi.ac.uk/efo/EFO_0800890 GCST90204042 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24556 levels 106 South Asian ancestry individuals NA Affymetrix [4411785] (imputed) 0 X-24556 measurement http://www.ebi.ac.uk/efo/EFO_0800895 GCST90204043 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25810 levels 103 East Asian ancestry individuals NA Affymetrix [4299391] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203083 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25828 levels 103 East Asian ancestry individuals NA Affymetrix [4298892] (imputed) 0 X-25828 measurement http://www.ebi.ac.uk/efo/EFO_0800936 GCST90203084 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25433 levels 84 East Asian ancestry individuals NA Affymetrix [4287361] (imputed) 0 X-25433 measurement http://www.ebi.ac.uk/efo/EFO_0800928 GCST90203085 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25519 levels 103 East Asian ancestry individuals NA Affymetrix [4298892] (imputed) 0 X-25519 measurement http://www.ebi.ac.uk/efo/EFO_0800930 GCST90203086 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25422 levels 102 East Asian ancestry individuals NA Affymetrix [4317062] (imputed) 0 X-25422 measurement http://www.ebi.ac.uk/efo/EFO_0800927 GCST90203087 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26054 levels 100 East Asian ancestry individuals NA Affymetrix [4351060] (imputed) 0 X-26054 measurement http://www.ebi.ac.uk/efo/EFO_0800939 GCST90203088 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25790 levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 X-25790 measurement http://www.ebi.ac.uk/efo/EFO_0800933 GCST90203089 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25420 levels 103 East Asian ancestry individuals NA Affymetrix [4302794] (imputed) 0 X-25420 measurement http://www.ebi.ac.uk/efo/EFO_0800926 GCST90203090 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26111 levels 94 East Asian ancestry individuals NA Affymetrix [4290223] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203091 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26109 levels 77 East Asian ancestry individuals NA Affymetrix [4220704] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203092 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine levels 107 South Asian ancestry individuals NA Affymetrix [4396920] (imputed) 0 carnitine measurement http://www.ebi.ac.uk/efo/EFO_0010469 GCST90203093 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Benzoate levels 99 South Asian ancestry individuals NA Affymetrix [4362544] (imputed) 0 benzoate measurement http://www.ebi.ac.uk/efo/EFO_0021150 GCST90203094 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycodeoxycholate levels 69 South Asian ancestry individuals NA Affymetrix [4292454] (imputed) 0 glycodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010493 GCST90203095 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tartarate levels 94 South Asian ancestry individuals NA Affymetrix [4451705] (imputed) 0 tartarate measurement http://www.ebi.ac.uk/efo/EFO_0800941 GCST90203096 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ribitol levels 104 South Asian ancestry individuals NA Affymetrix [4446938] (imputed) 0 ribitol measurement http://www.ebi.ac.uk/efo/EFO_0800143 GCST90203097 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Theophylline levels 100 South Asian ancestry individuals NA Affymetrix [4525757] (imputed) 0 theophylline measurement http://www.ebi.ac.uk/efo/EFO_0021180 GCST90203098 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-alpha-acetylornithine levels 70 South Asian ancestry individuals NA Affymetrix [4563883] (imputed) 0 N-alpha-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800006 GCST90203099 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Suberate (C8-DC) levels 88 South Asian ancestry individuals NA Affymetrix [4333954] (imputed) 0 suberate (C8-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800181 GCST90203100 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetate levels 73 South Asian ancestry individuals NA Affymetrix [4465142] (imputed) 0 phenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0021012 GCST90203101 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Maltotriose levels 65 South Asian ancestry individuals NA Affymetrix [4372026] (imputed) 0 maltotriose measurement http://www.ebi.ac.uk/efo/EFO_0800142 GCST90203102 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphorylcholine (GPC) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 glycerophosphorylcholine measurement http://www.ebi.ac.uk/efo/EFO_0020018 GCST90203103 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfoxide levels 107 South Asian ancestry individuals NA Affymetrix [4392431] (imputed) 0 Methionine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0021650 GCST90203104 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-guanidinobutanoate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 4-guanidinobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0800003 GCST90203105 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole lactate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 imidazole lactate measurement http://www.ebi.ac.uk/efo/EFO_0800004 GCST90203106 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylhistidine levels 107 South Asian ancestry individuals NA Affymetrix [4395279] (imputed) 0 3-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0021004 GCST90203107 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17351 levels 85 East Asian ancestry individuals NA Affymetrix [4259831] (imputed) 0 X-17351 measurement http://www.ebi.ac.uk/efo/EFO_0800774 GCST90202970 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17010 levels 96 East Asian ancestry individuals NA Affymetrix [4257256] (imputed) 0 X-17010 measurement http://www.ebi.ac.uk/efo/EFO_0800767 GCST90202971 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17654 levels 91 East Asian ancestry individuals NA Affymetrix [4335802] (imputed) 0 X-17654 measurement http://www.ebi.ac.uk/efo/EFO_0800784 GCST90202972 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16935 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-16935 measurement http://www.ebi.ac.uk/efo/EFO_0800763 GCST90202973 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17335 levels 96 East Asian ancestry individuals NA Affymetrix [4249708] (imputed) 0 X-17335 measurement http://www.ebi.ac.uk/efo/EFO_0800772 GCST90202974 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16964 levels 100 East Asian ancestry individuals NA Affymetrix [4349628] (imputed) 0 X-16964 measurement http://www.ebi.ac.uk/efo/EFO_0020011 GCST90202975 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-16580 levels 102 East Asian ancestry individuals NA Affymetrix [4322154] (imputed) 0 X-16580 measurement http://www.ebi.ac.uk/efo/EFO_0800761 GCST90202976 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17357 levels 102 East Asian ancestry individuals NA Affymetrix [4318311] (imputed) 0 X-17357 measurement http://www.ebi.ac.uk/efo/EFO_0800777 GCST90202977 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15503 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-15503 measurement http://www.ebi.ac.uk/efo/EFO_0800753 GCST90202978 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15523 levels 102 East Asian ancestry individuals NA Affymetrix [4320335] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202979 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15728 levels 89 East Asian ancestry individuals NA Affymetrix [4185803] (imputed) 0 X-15728 measurement http://www.ebi.ac.uk/efo/EFO_0020024 GCST90202980 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-15486 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-15486 measurement http://www.ebi.ac.uk/efo/EFO_0800751 GCST90202981 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17685 levels 91 East Asian ancestry individuals NA Affymetrix [4336842] (imputed) 0 X-17685 measurement http://www.ebi.ac.uk/efo/EFO_0800786 GCST90202982 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19299 levels 76 East Asian ancestry individuals NA Affymetrix [4246735] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202983 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21283 levels 87 East Asian ancestry individuals NA Affymetrix [4214629] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202984 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19438 levels 90 East Asian ancestry individuals NA Affymetrix [4352362] (imputed) 0 X-19438 measurement http://www.ebi.ac.uk/efo/EFO_0800801 GCST90202985 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-19141 levels 103 East Asian ancestry individuals NA Affymetrix [4299282] (imputed) 0 X-19141 measurement http://www.ebi.ac.uk/efo/EFO_0800799 GCST90202986 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21258 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-21258 measurement http://www.ebi.ac.uk/efo/EFO_0800802 GCST90202987 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18913 levels 103 East Asian ancestry individuals NA Affymetrix [4305995] (imputed) 0 X-18913 measurement http://www.ebi.ac.uk/efo/EFO_0800795 GCST90202988 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18901 levels 99 East Asian ancestry individuals NA Affymetrix [4189169] (imputed) 0 X-18901 measurement http://www.ebi.ac.uk/efo/EFO_0800794 GCST90202989 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21310 levels 98 East Asian ancestry individuals NA Affymetrix [4211982] (imputed) 0 X-21310 measurement http://www.ebi.ac.uk/efo/EFO_0800805 GCST90202990 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18922 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-18922 measurement http://www.ebi.ac.uk/efo/EFO_0800797 GCST90202991 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21286 levels 103 East Asian ancestry individuals NA Affymetrix [4300629] (imputed) 0 X-21286 measurement http://www.ebi.ac.uk/efo/EFO_0800804 GCST90202992 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21285 levels 90 East Asian ancestry individuals NA Affymetrix [4364368] (imputed) 0 X-21285 measurement http://www.ebi.ac.uk/efo/EFO_0800803 GCST90202993 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18921 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-18921 measurement http://www.ebi.ac.uk/efo/EFO_0800796 GCST90202994 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21807 levels 58 East Asian ancestry individuals NA Affymetrix [4162307] (imputed) 0 X-21807 measurement http://www.ebi.ac.uk/efo/EFO_0800827 GCST90203020 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21821 levels 90 East Asian ancestry individuals NA Affymetrix [4353599] (imputed) 0 X-21821 measurement http://www.ebi.ac.uk/efo/EFO_0800829 GCST90203021 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22520 levels 62 East Asian ancestry individuals NA Affymetrix [4331632] (imputed) 0 X-22520 measurement http://www.ebi.ac.uk/efo/EFO_0800843 GCST90203022 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22771 levels 102 East Asian ancestry individuals NA Affymetrix [4316705] (imputed) 0 X-22771 measurement http://www.ebi.ac.uk/efo/EFO_0800844 GCST90203023 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22776 levels 91 East Asian ancestry individuals NA Affymetrix [4334022] (imputed) 0 X-22776 measurement http://www.ebi.ac.uk/efo/EFO_0800845 GCST90203024 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22834 levels 80 East Asian ancestry individuals NA Affymetrix [4354346] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203025 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23636 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-23636 measurement http://www.ebi.ac.uk/efo/EFO_0800852 GCST90203026 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23276 levels 85 East Asian ancestry individuals NA Affymetrix [4256762] (imputed) 0 X-23276 measurement http://www.ebi.ac.uk/efo/EFO_0800847 GCST90203027 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23593 levels 102 East Asian ancestry individuals NA Affymetrix [4316196] (imputed) 0 X-23593 measurement http://www.ebi.ac.uk/efo/EFO_0800851 GCST90203028 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23587 levels 99 East Asian ancestry individuals NA Affymetrix [4199880] (imputed) 0 X-23587 measurement http://www.ebi.ac.uk/efo/EFO_0800849 GCST90203029 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23639 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-23639 measurement http://www.ebi.ac.uk/efo/EFO_0800853 GCST90203030 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23782 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-23782 measurement http://www.ebi.ac.uk/efo/EFO_0800865 GCST90203031 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23644 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-23644 measurement http://www.ebi.ac.uk/efo/EFO_0800855 GCST90203032 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23655 levels 73 East Asian ancestry individuals NA Affymetrix [4316100] (imputed) 0 X-23655 measurement http://www.ebi.ac.uk/efo/EFO_0800856 GCST90203033 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23654 levels 103 East Asian ancestry individuals NA Affymetrix [4295850] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203034 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23648 levels 100 East Asian ancestry individuals NA Affymetrix [4353035] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203035 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23678 levels 63 East Asian ancestry individuals NA Affymetrix [4320533] (imputed) 0 X-23678 measurement http://www.ebi.ac.uk/efo/EFO_0800861 GCST90203036 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23665 levels 102 East Asian ancestry individuals NA Affymetrix [4320587] (imputed) 0 X-23665 measurement http://www.ebi.ac.uk/efo/EFO_0800859 GCST90203037 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23680 levels 103 East Asian ancestry individuals NA Affymetrix [4300838] (imputed) 0 X-23680 measurement http://www.ebi.ac.uk/efo/EFO_0800862 GCST90203038 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23780 levels 101 East Asian ancestry individuals NA Affymetrix [4335157] (imputed) 0 X-23780 measurement http://www.ebi.ac.uk/efo/EFO_0800864 GCST90203039 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24243 levels 98 East Asian ancestry individuals NA Affymetrix [4213042] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203040 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23997 levels 92 East Asian ancestry individuals NA Affymetrix [4328278] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90203041 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23641 levels 87 East Asian ancestry individuals NA Affymetrix [4238469] (imputed) 0 X-23641 measurement http://www.ebi.ac.uk/efo/EFO_0800854 GCST90203042 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24241 levels 100 East Asian ancestry individuals NA Affymetrix [4350900] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203043 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23974 levels 100 East Asian ancestry individuals NA Affymetrix [4344465] (imputed) 0 X-23974 measurement http://www.ebi.ac.uk/efo/EFO_0800867 GCST90203044 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17690 levels 75 East Asian ancestry individuals NA Affymetrix [4259037] (imputed) 0 X-17690 measurement http://www.ebi.ac.uk/efo/EFO_0800788 GCST90202995 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21319 levels 100 East Asian ancestry individuals NA Affymetrix [4354609] (imputed) 0 X-21319 measurement http://www.ebi.ac.uk/efo/EFO_0800807 GCST90202996 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18779 levels 103 East Asian ancestry individuals NA Affymetrix [4299732] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202997 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18888 levels 88 East Asian ancestry individuals NA Affymetrix [4205584] (imputed) 0 X-18888 measurement http://www.ebi.ac.uk/efo/EFO_0800792 GCST90202998 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18886 levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 X-18886 measurement http://www.ebi.ac.uk/efo/EFO_0800790 GCST90202999 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-18887 levels 85 East Asian ancestry individuals NA Affymetrix [4285927] (imputed) 0 X-18887 measurement http://www.ebi.ac.uk/efo/EFO_0800791 GCST90203000 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-17676 levels 102 East Asian ancestry individuals NA Affymetrix [4319638] (imputed) 0 X-17676 measurement http://www.ebi.ac.uk/efo/EFO_0800785 GCST90203001 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21353 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-21353 measurement http://www.ebi.ac.uk/efo/EFO_0800809 GCST90203002 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21355 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-21355 measurement http://www.ebi.ac.uk/efo/EFO_0800810 GCST90203003 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21441 levels 101 East Asian ancestry individuals NA Affymetrix [4327299] (imputed) 0 X-21441 measurement http://www.ebi.ac.uk/efo/EFO_0800814 GCST90203004 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21471 levels 102 East Asian ancestry individuals NA Affymetrix [4316150] (imputed) 0 X-21471 measurement http://www.ebi.ac.uk/efo/EFO_0800818 GCST90203005 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21733 levels 84 East Asian ancestry individuals NA Affymetrix [4300770] (imputed) 0 X-21733 measurement http://www.ebi.ac.uk/efo/EFO_0800820 GCST90203006 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21607 levels 103 East Asian ancestry individuals NA Affymetrix [4300600] (imputed) 0 X-21607 measurement http://www.ebi.ac.uk/efo/EFO_0800819 GCST90203007 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21383 levels 101 East Asian ancestry individuals NA Affymetrix [4331518] (imputed) 0 X-21383 measurement http://www.ebi.ac.uk/efo/EFO_0800812 GCST90203008 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21467 levels 103 East Asian ancestry individuals NA Affymetrix [4298515] (imputed) 0 X-21467 measurement http://www.ebi.ac.uk/efo/EFO_0020007 GCST90203009 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21470 levels 100 East Asian ancestry individuals NA Affymetrix [4344692] (imputed) 0 X-21470 measurement http://www.ebi.ac.uk/efo/EFO_0800817 GCST90203010 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21339 levels 103 East Asian ancestry individuals NA Affymetrix [4298445] (imputed) 0 X-21339 measurement http://www.ebi.ac.uk/efo/EFO_0800808 GCST90203011 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21742 levels 71 East Asian ancestry individuals NA Affymetrix [4361126] (imputed) 0 X-21742 measurement http://www.ebi.ac.uk/efo/EFO_0800823 GCST90203012 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21796 levels 103 East Asian ancestry individuals NA Affymetrix [4299195] (imputed) 0 X-21796 measurement http://www.ebi.ac.uk/efo/EFO_0800825 GCST90203013 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21752 levels 62 East Asian ancestry individuals NA Affymetrix [4327943] (imputed) 0 X-21752 measurement http://www.ebi.ac.uk/efo/EFO_0800824 GCST90203014 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-22162 levels 103 East Asian ancestry individuals NA Affymetrix [4300838] (imputed) 0 X-22162 measurement http://www.ebi.ac.uk/efo/EFO_0800839 GCST90203015 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21829 levels 102 East Asian ancestry individuals NA Affymetrix [4319998] (imputed) 0 X-21829 measurement http://www.ebi.ac.uk/efo/EFO_0800830 GCST90203016 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21834 levels 91 East Asian ancestry individuals NA Affymetrix [4349999] (imputed) 0 X-21834 measurement http://www.ebi.ac.uk/efo/EFO_0800833 GCST90203017 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21442 levels 77 East Asian ancestry individuals NA Affymetrix [4218969] (imputed) 0 X-21442 measurement http://www.ebi.ac.uk/efo/EFO_0800815 GCST90203018 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-21364 levels 103 East Asian ancestry individuals NA Affymetrix [4300420] (imputed) 0 X-21364 measurement http://www.ebi.ac.uk/efo/EFO_0800811 GCST90203019 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24544 levels 104 South Asian ancestry individuals NA Affymetrix [4446312] (imputed) 0 X-24544 measurement http://www.ebi.ac.uk/efo/EFO_0800892 GCST90204036 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24588 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-24588 measurement http://www.ebi.ac.uk/efo/EFO_0800898 GCST90203059 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24757 levels 66 East Asian ancestry individuals NA Affymetrix [4254570] (imputed) 0 X-24757 measurement http://www.ebi.ac.uk/efo/EFO_0800905 GCST90203060 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24565 levels 51 East Asian ancestry individuals NA Affymetrix [4374194] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203061 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24812 levels 96 East Asian ancestry individuals NA Affymetrix [4240949] (imputed) 0 X-24812 measurement http://www.ebi.ac.uk/efo/EFO_0800908 GCST90203062 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24801 levels 102 East Asian ancestry individuals NA Affymetrix [4319806] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203063 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24728 levels 103 East Asian ancestry individuals NA Affymetrix [4300331] (imputed) 0 X-24728 measurement http://www.ebi.ac.uk/efo/EFO_0800903 GCST90203064 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24811 levels 61 East Asian ancestry individuals NA Affymetrix [4386983] (imputed) 0 X-24811 measurement http://www.ebi.ac.uk/efo/EFO_0800907 GCST90203065 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24585 levels 103 East Asian ancestry individuals NA Affymetrix [4305995] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203066 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24544 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-24544 measurement http://www.ebi.ac.uk/efo/EFO_0800892 GCST90203067 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24334 levels 85 East Asian ancestry individuals NA Affymetrix [4275606] (imputed) 0 X-24334 measurement http://www.ebi.ac.uk/efo/EFO_0800874 GCST90203068 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24795 levels 57 East Asian ancestry individuals NA Affymetrix [4198953] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203069 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24531 levels 57 East Asian ancestry individuals NA Affymetrix [4219087] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203070 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24951 levels 102 East Asian ancestry individuals NA Affymetrix [4317595] (imputed) 0 X-24951 measurement http://www.ebi.ac.uk/efo/EFO_0800912 GCST90203071 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24970 levels 103 East Asian ancestry individuals NA Affymetrix [4301000] (imputed) 0 X-24970 measurement http://www.ebi.ac.uk/efo/EFO_0800913 GCST90203072 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25109 levels 97 East Asian ancestry individuals NA Affymetrix [4218505] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203073 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25265 levels 98 East Asian ancestry individuals NA Affymetrix [4207788] (imputed) 0 X-25265 measurement http://www.ebi.ac.uk/efo/EFO_0800917 GCST90203074 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25371 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-25371 measurement http://www.ebi.ac.uk/efo/EFO_0800923 GCST90203075 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25172 levels 103 East Asian ancestry individuals NA Affymetrix [4298428] (imputed) 0 X-25172 measurement http://www.ebi.ac.uk/efo/EFO_0800916 GCST90203076 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25271 levels 101 East Asian ancestry individuals NA Affymetrix [4341119] (imputed) 0 X-25271 measurement http://www.ebi.ac.uk/efo/EFO_0800920 GCST90203077 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24949 levels 101 East Asian ancestry individuals NA Affymetrix [4334065] (imputed) 0 X-24949 measurement http://www.ebi.ac.uk/efo/EFO_0800911 GCST90203078 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25520 levels 97 East Asian ancestry individuals NA Affymetrix [4224771] (imputed) 0 X-25520 measurement http://www.ebi.ac.uk/efo/EFO_0800931 GCST90203079 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25419 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-25419 measurement http://www.ebi.ac.uk/efo/EFO_0800925 GCST90203080 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25343 levels 103 East Asian ancestry individuals NA Affymetrix [4301041] (imputed) 0 X-25343 measurement http://www.ebi.ac.uk/efo/EFO_0800922 GCST90203081 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25957 levels 95 East Asian ancestry individuals NA Affymetrix [4279264] (imputed) 0 X-25957 measurement http://www.ebi.ac.uk/efo/EFO_0800938 GCST90203082 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24328 levels 101 East Asian ancestry individuals NA Affymetrix [4331257] (imputed) 0 X-24328 measurement http://www.ebi.ac.uk/efo/EFO_0800873 GCST90203045 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24295 levels 102 East Asian ancestry individuals NA Affymetrix [4314414] (imputed) 0 X-24295 measurement http://www.ebi.ac.uk/efo/EFO_0800869 GCST90203046 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24307 levels 103 East Asian ancestry individuals NA Affymetrix [4301041] (imputed) 0 X-24307 measurement http://www.ebi.ac.uk/efo/EFO_0800871 GCST90203047 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24306 levels 102 East Asian ancestry individuals NA Affymetrix [4315969] (imputed) 0 X-24306 measurement http://www.ebi.ac.uk/efo/EFO_0800870 GCST90203048 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23659 levels 102 East Asian ancestry individuals NA Affymetrix [4316871] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90203049 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23739 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-23739 measurement http://www.ebi.ac.uk/efo/EFO_0800863 GCST90203050 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24546 levels 98 East Asian ancestry individuals NA Affymetrix [4211574] (imputed) 0 X-24546 measurement http://www.ebi.ac.uk/efo/EFO_0800893 GCST90203051 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24556 levels 99 East Asian ancestry individuals NA Affymetrix [4194962] (imputed) 0 X-24556 measurement http://www.ebi.ac.uk/efo/EFO_0800895 GCST90203052 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24947 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 X-24947 measurement http://www.ebi.ac.uk/efo/EFO_0800910 GCST90203053 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24418 levels 74 East Asian ancestry individuals NA Affymetrix [4275055] (imputed) 0 X-24418 measurement http://www.ebi.ac.uk/efo/EFO_0800879 GCST90203054 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24456 levels 86 East Asian ancestry individuals NA Affymetrix [4238876] (imputed) 0 X-24456 measurement http://www.ebi.ac.uk/efo/EFO_0800885 GCST90203055 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24518 levels 56 East Asian ancestry individuals NA Affymetrix [4242549] (imputed) 0 X-24518 measurement http://www.ebi.ac.uk/efo/EFO_0800890 GCST90203056 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24337 levels 100 East Asian ancestry individuals NA Affymetrix [4353246] (imputed) 0 X-24337 measurement http://www.ebi.ac.uk/efo/EFO_0800875 GCST90203057 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24494 levels 85 East Asian ancestry individuals NA Affymetrix [4271965] (imputed) 0 X-24494 measurement http://www.ebi.ac.uk/efo/EFO_0800889 GCST90203058 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24241 levels 106 South Asian ancestry individuals NA Affymetrix [4416988] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204025 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24243 levels 92 South Asian ancestry individuals NA Affymetrix [4494145] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204026 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24337 levels 103 South Asian ancestry individuals NA Affymetrix [4482769] (imputed) 0 X-24337 measurement http://www.ebi.ac.uk/efo/EFO_0800875 GCST90204027 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24334 levels 92 South Asian ancestry individuals NA Affymetrix [4499607] (imputed) 0 X-24334 measurement http://www.ebi.ac.uk/efo/EFO_0800874 GCST90204028 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24418 levels 70 South Asian ancestry individuals NA Affymetrix [4569170] (imputed) 0 X-24418 measurement http://www.ebi.ac.uk/efo/EFO_0800879 GCST90204029 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24456 levels 80 South Asian ancestry individuals NA Affymetrix [4545427] (imputed) 0 X-24456 measurement http://www.ebi.ac.uk/efo/EFO_0800885 GCST90204030 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24494 levels 78 South Asian ancestry individuals NA Affymetrix [4362805] (imputed) 0 X-24494 measurement http://www.ebi.ac.uk/efo/EFO_0800889 GCST90204031 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24757 levels 68 South Asian ancestry individuals NA Affymetrix [4337543] (imputed) 0 X-24757 measurement http://www.ebi.ac.uk/efo/EFO_0800905 GCST90204032 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24811 levels 57 South Asian ancestry individuals NA Affymetrix [4340637] (imputed) 0 X-24811 measurement http://www.ebi.ac.uk/efo/EFO_0800907 GCST90204033 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24801 levels 105 South Asian ancestry individuals NA Affymetrix [4430461] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204034 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24728 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-24728 measurement http://www.ebi.ac.uk/efo/EFO_0800903 GCST90204035 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_446) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279331 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4461) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279332 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4466) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279333 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4467) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279334 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_447) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279335 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4472) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279336 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4480) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279337 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4499) (4E15Z-Bilirubin IXa) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279338 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_450) (Sulfoacetate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279339 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4525) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279340 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4526) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279341 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_453) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279342 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4540) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279343 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4541) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279344 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4544) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279345 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4545) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279346 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4546) (4-Hydroxyanigorootin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 4-hydroxyanigorootin measurement http://www.ebi.ac.uk/efo/EFO_0803390 GCST90279347 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4551) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279348 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4553) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279349 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4555) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 14 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279350 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_456) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 63 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279351 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4565) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279352 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_457) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279353 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4582) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279354 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4583) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 68 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279355 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4687) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279377 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4691) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279378 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4693) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279379 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4699) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279380 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_47) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279381 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4700) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279382 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4703) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279383 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4704) (1-(5Z8Z11Z14Z17Z-eicosapentaenoyl)-glycero-3-phospho-(1-myo-inositol)) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 level of 1-(5Z,8Z,11Z,14Z,17Z-eicosapentaenoyl)-sn-glycero-3-phospho-1D-myo-inositol in blood serum http://purl.obolibrary.org/obo/OBA_2045059 GCST90279384 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4705) (Minosaminomycin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 minosaminomycin measurement http://www.ebi.ac.uk/efo/EFO_0803504 GCST90279385 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4706) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279386 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4708) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279387 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4715) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279388 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4716) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279389 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4722) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279390 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4724) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279391 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4727) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279392 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4733) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279393 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_474) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279394 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4744) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279395 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4745) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279396 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4748) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279397 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4756) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279398 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4762) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279399 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4767) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279400 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4768) (N-(15Z-tetracosenoyl)-1-deoxysphing-4-enine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 level of ceramide in blood serum http://purl.obolibrary.org/obo/OBA_2045029 GCST90279401 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3735) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280104 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3740) (N-Acetyldehydroanonaine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 N-acetyldehydroanonaine measurement http://www.ebi.ac.uk/efo/EFO_0803436 GCST90280105 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3751) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280106 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3759) (Quinoxyfen) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 quinoxyfen measurement http://www.ebi.ac.uk/efo/EFO_0803511 GCST90280107 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3761) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280108 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3762) (Erysopine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280109 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3763) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280110 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3770) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280111 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3777) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280112 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3781) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280113 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_379) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280114 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4618) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279363 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4634) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279364 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4635) (Janthitrem E) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279365 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4641) (Phaeophorbide b) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 10 phaeophorbide b measurement http://www.ebi.ac.uk/efo/EFO_0803447 GCST90279366 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4647) (Phaeophorbide b) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 49 phaeophorbide b measurement http://www.ebi.ac.uk/efo/EFO_0803447 GCST90279367 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4649) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279368 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_465) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279369 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4650) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279370 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4659) (Somniferine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 somniferine measurement http://www.ebi.ac.uk/efo/EFO_0803455 GCST90279371 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4660) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279372 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4661) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279373 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4663) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279374 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4666) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279375 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4674) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279376 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_477) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279402 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4773) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279403 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_478) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279404 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4784) (Perphenazine maleate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 perphenazine maleate measurement http://www.ebi.ac.uk/efo/EFO_0803506 GCST90279405 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_480) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279406 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4803) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279407 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4804) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279408 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4805) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279409 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4809) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279410 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4814) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279411 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4819) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 17 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279412 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4826) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279413 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4835) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279414 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4842) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279415 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4845) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279416 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4850) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279417 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4867) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279418 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4868) (Scutianine F) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 scutianine F measurement http://www.ebi.ac.uk/efo/EFO_0803514 GCST90279419 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4873) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279420 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4876) (Pentasine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 pentasine measurement http://www.ebi.ac.uk/efo/EFO_0803445 GCST90279421 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4878) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279422 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_380) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280115 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3802) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280116 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3803) (N-Hexadecanoylpyrrolidine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 N-hexadecanoylpyrrolidine measurement http://www.ebi.ac.uk/efo/EFO_0803438 GCST90280117 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3808) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280118 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3818) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280119 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3823) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280120 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3836) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280121 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_384) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280122 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3851) (N-(Heptadecanoyl)-ethanolamine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 level of Margaroyl-EA in blood serum http://purl.obolibrary.org/obo/OBA_2045042 GCST90280123 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3855) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280124 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3867) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280125 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3873) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280126 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3874) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280127 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3878) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280128 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3890) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280129 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_39) (Ethyl thiocyanate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 ethyl thiocyanate measurement http://www.ebi.ac.uk/efo/EFO_0803525 GCST90280130 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3901) ((9S10S)-910-dihydroxyoctadecanoate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280131 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3902) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280132 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3904) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280133 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3909) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 12 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280134 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3920) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280135 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3928) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280136 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3941) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280137 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3951) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280138 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_396) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280139 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3960) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280140 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3965) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280141 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3966) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280142 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3967) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280143 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4134) (Nicotinic acid mononucleotide) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 nicotinic acid mononucleotide measurement http://www.ebi.ac.uk/efo/EFO_0803441 GCST90280169 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4144) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280170 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4147) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280171 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4158) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280172 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4166) (Phenylmercuric borate) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 phenylmercuric borate measurement http://www.ebi.ac.uk/efo/EFO_0803529 GCST90280173 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4880) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279423 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4889) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279424 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_49) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279425 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_490) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279426 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_492) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279427 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4934) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279428 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4936) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279429 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4937) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279430 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4962) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279431 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_4972) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279432 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_50) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279433 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_501) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279434 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5010) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279435 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5027) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279436 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_503) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279437 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5031) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 7 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279438 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5035) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279439 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5052) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279440 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5054) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 16 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279441 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5055) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279442 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3968) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280144 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3976) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280145 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4004) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280146 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4006) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280147 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4007) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280148 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4018) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280149 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4019) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280150 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4024) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280151 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4031) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280152 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4032) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 5 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280153 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4042) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280154 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_405) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280155 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4056) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280156 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4067) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280157 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4072) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280158 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4074) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280159 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4078) (Sulfadimethoxine sodium) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 sulfadimethoxine sodium measurement http://www.ebi.ac.uk/efo/EFO_0803517 GCST90280160 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4084) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280161 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4088) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280162 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4093) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280163 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4105) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280164 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_411) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280165 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4112) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280166 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4123) (Musanolone D) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280167 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_4125) (S-Japonin) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 S-japonin measurement http://www.ebi.ac.uk/efo/EFO_0803453 GCST90280168 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_360) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280079 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3600) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280080 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3604) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280081 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_361) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280082 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3619) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280083 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3621) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280084 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3636) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280085 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3640) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280086 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3644) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280087 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3651) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280088 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3653) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 6 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280089 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3661) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280090 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3665) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280091 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3669) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280092 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3673) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 8 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280093 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3676) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280094 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3690) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280095 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3691) (Sphinganine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 sphinganine measurement http://www.ebi.ac.uk/efo/EFO_0800619 GCST90280096 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3692) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280097 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3699) (Pisatoside) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280098 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3704) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280099 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3705) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280100 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3706) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280101 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3712) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280102 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (hilic_3719) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90280103 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5060) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279443 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5068) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279444 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5069) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279445 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_507) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279446 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5071) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279447 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5092) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279448 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_510) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279449 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5102) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279450 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5105) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279451 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5111) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279452 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5131) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279453 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5141) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279454 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5144) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279455 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5147) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279456 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5149) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 2 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279457 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5151) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279458 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5153) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279459 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5156) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 15 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279460 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5160) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279461 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_517) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279462 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5170) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279463 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5175) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279464 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_5179) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 3 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279465 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_519) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 1 blood metabolite measurement http://www.ebi.ac.uk/efo/EFO_0005664 GCST90279466 Genome-wide genotyping array 2023-09-01 36482414 Lee IH 2022-12-08 Hum Genomics www.ncbi.nlm.nih.gov/pubmed/36482414 Comprehensive characterization of putative genetic influences on plasma metabolome in a pediatric cohort. Plasma metabolome feature (c18_520) (Lysine) 7 Asian ancestry children, 36 Black or African American children, 352 European ancestry children, 1 Native Hawaiian or other Pacific Islander child, 45 children NA Illumina [619688] 4 lysine measurement http://www.ebi.ac.uk/efo/EFO_0005002 GCST90279467 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methyluridine (ribothymidine) levels 8,168 European ancestry individuals NA Affymetrix [15425756] (imputed) 4 5-methyluridine (ribothymidine) measurement http://www.ebi.ac.uk/efo/EFO_0020013 GCST90199783 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cysteine-glutathione disulfide levels 7,812 European ancestry individuals NA Affymetrix [15412400] (imputed) 1 cysteine-glutathione disulfide measurement http://www.ebi.ac.uk/efo/EFO_0021001 GCST90199784 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerylglycine levels 7,100 European ancestry individuals NA Affymetrix [15377875] (imputed) 1 isovalerylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800025 GCST90199785 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxy-3-methylvalerate levels 8,246 European ancestry individuals NA Affymetrix [15430196] (imputed) 2 2-hydroxy-3-methylvalerate measurement http://www.ebi.ac.uk/efo/EFO_0800027 GCST90199786 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homostachydrine levels 8,248 European ancestry individuals NA Affymetrix [15430710] (imputed) 2 homostachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021164 GCST90199787 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonoyl-gpc (20:4n6) levels 8,267 European ancestry individuals NA Affymetrix [15431209] (imputed) 3 1-arachidonoyl-GPC (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800234 GCST90199788 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-palmitoyl-GPC (16:0) levels 8,249 European ancestry individuals NA Affymetrix [15429100] (imputed) 1 2-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800241 GCST90199789 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-palmitoleoyl-GPC (16:1) levels 6,697 European ancestry individuals NA Affymetrix [15368612] (imputed) 1 2-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800240 GCST90199790 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonoyl-GPE (20:4n6) levels 8,270 European ancestry individuals NA Affymetrix [15431214] (imputed) 4 1-arachidonoyl-GPE (20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800248 GCST90199791 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPE (16:0) levels 8,276 European ancestry individuals NA Affymetrix [15431695] (imputed) 4 1-palmitoyl-GPE (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800245 GCST90199792 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPE (18:2) levels 8,279 European ancestry individuals NA Affymetrix [15431550] (imputed) 3 1-linoleoyl-GPE (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800247 GCST90199793 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPE (18:1) levels 8,283 European ancestry individuals NA Affymetrix [15431821] (imputed) 1 1-oleoyl-GPE (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800246 GCST90199794 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxypalmitate levels 8,247 European ancestry individuals NA Affymetrix [15429034] (imputed) 0 2-hydroxypalmitate measurement http://www.ebi.ac.uk/efo/EFO_0021507 GCST90199795 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate (n6 DPA; 22:5n6) levels 7,540 European ancestry individuals NA Affymetrix [15396940] (imputed) 1 docosapentaenoate (n6 DPA; 22:5n6) measurement http://www.ebi.ac.uk/efo/EFO_0800249 GCST90199796 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gulonate levels 7,731 European ancestry individuals NA Affymetrix [15408876] (imputed) 0 gulonate measurement http://www.ebi.ac.uk/efo/EFO_0800159 GCST90199797 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isobutyrylglycine levels 7,465 European ancestry individuals NA Affymetrix [15394379] (imputed) 2 isobutyrylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800029 GCST90199798 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutarylcarnitine (c5-dc) levels 8,238 European ancestry individuals NA Affymetrix [15430922] (imputed) 9 glutarylcarnitine (C5-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800030 GCST90199799 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C5:1 levels 8,097 European ancestry individuals NA Affymetrix [15425180] (imputed) 1 tiglylcarnitine (C5:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800032 GCST90199800 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hydroquinone sulfate levels 7,682 European ancestry individuals NA Affymetrix [15406574] (imputed) 0 hydroquinone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021157 GCST90199801 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovaleroylcarnitine levels 8,232 European ancestry individuals NA Affymetrix [15429018] (imputed) 3 beta-hydroxyisovaleroylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800031 GCST90199802 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Catechol sulfate levels 8,242 European ancestry individuals NA Affymetrix [15430757] (imputed) 0 catechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021151 GCST90199803 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-alpha-hydroxy-3-oxo-4-cholestenoate (7-hoca) levels 8,236 European ancestry individuals NA Affymetrix [15429851] (imputed) 1 7-alpha-hydroxy-3-oxo-4-cholestenoate 7-Hoca measurement http://www.ebi.ac.uk/efo/EFO_0021116 GCST90199804 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioate levels 8,223 European ancestry individuals NA Affymetrix [15429412] (imputed) 2 octadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021056 GCST90199805 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetradecanedioate (C14-DC) levels 8,268 European ancestry individuals NA Affymetrix [15431625] (imputed) 3 tetradecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021057 GCST90199806 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecanedioate (C16-DC) levels 8,260 European ancestry individuals NA Affymetrix [15431581] (imputed) 2 hexadecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0021055 GCST90199807 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydecanoylcarnitine levels 8,237 European ancestry individuals NA Affymetrix [15429893] (imputed) 0 3-hydroxydecanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800590 GCST90200246 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Levulinoylcarnitine levels 7,197 European ancestry individuals NA Affymetrix [15384093] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200247 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis 3,4-methyleneheptanoate levels 8,223 European ancestry individuals NA Affymetrix [15429252] (imputed) 1 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90200248 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels 8,256 European ancestry individuals NA Affymetrix [15430938] (imputed) 2 branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid measurement http://www.ebi.ac.uk/efo/EFO_0800662 GCST90200249 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycholic acid 12-sulfate levels 7,438 European ancestry individuals NA Affymetrix [15401552] (imputed) 4 deoxycholic acid (12 or 24)-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800599 GCST90200250 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) levels 8,265 European ancestry individuals NA Affymetrix [15429498] (imputed) 0 branched-chain, straight-chain, or cyclopropyl 10:1 fatty acid (1) measurement http://www.ebi.ac.uk/efo/EFO_0800661 GCST90200251 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,5-dichloro-2,6-dihydroxybenzoic acid levels 8,218 European ancestry individuals NA Affymetrix [15429319] (imputed) 1 3,5-dichloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801054 GCST90200252 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic acid glycine levels 7,512 European ancestry individuals NA Affymetrix [15399584] (imputed) 3 vanillic acid glycine measurement http://www.ebi.ac.uk/efo/EFO_0801056 GCST90200253 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-a-amino-omega-caprolactam levels 8,185 European ancestry individuals NA Affymetrix [15429519] (imputed) 0 (S)-a-amino-omega-caprolactam measurement http://www.ebi.ac.uk/efo/EFO_0801055 GCST90200254 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-bromo-5-chloro-2,6-dihydroxybenzoic acid levels 8,127 European ancestry individuals NA Affymetrix [15426099] (imputed) 1 3-bromo-5-chloro-2,6-dihydroxybenzoic acid measurement http://www.ebi.ac.uk/efo/EFO_0801058 GCST90200255 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dibutyl sulfosuccinate levels 8,099 European ancestry individuals NA Affymetrix [15426122] (imputed) 0 blood dibutyl sulfosuccinate measurement http://www.ebi.ac.uk/efo/EFO_0022212 GCST90200256 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Metabolonic lactone sulfate levels 8,203 European ancestry individuals NA Affymetrix [15429181] (imputed) 7 metabolonic lactone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800659 GCST90200257 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxy-4-(methylthio)butanoic acid levels 8,255 European ancestry individuals NA Affymetrix [15430769] (imputed) 3 2-hydroxy-4-(methylthio)butanoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800113 GCST90200258 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pentose acid levels 8,235 European ancestry individuals NA Affymetrix [15430276] (imputed) 0 pentose acid measurement http://www.ebi.ac.uk/efo/EFO_0800660 GCST90200259 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Branched chain 14:0 dicarboxylic acid levels 7,990 European ancestry individuals NA Affymetrix [15419400] (imputed) 0 branched chain 14:0 dicarboxylic acid measurement http://www.ebi.ac.uk/efo/EFO_0800593 GCST90200260 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-carboxyethylcysteine levels 8,010 European ancestry individuals NA Affymetrix [15422965] (imputed) 1 L-Cysteine measurement http://www.ebi.ac.uk/efo/EFO_0021614 GCST90200261 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-succinyl-phenylalanine levels 6,199 European ancestry individuals NA Affymetrix [15334862] (imputed) 2 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200262 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (2 or 3)-decenoate (10:1n7 or n8) levels 8,124 European ancestry individuals NA Affymetrix [15426076] (imputed) 2 (2 or 3)-decenoate (10:1n7 or n8) measurement http://www.ebi.ac.uk/efo/EFO_0800594 GCST90200263 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (2) levels 8,254 European ancestry individuals NA Affymetrix [15430674] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200264 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (4) levels 8,159 European ancestry individuals NA Affymetrix [15427305] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200265 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylcarnitine levels 8,259 European ancestry individuals NA Affymetrix [15430951] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200266 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tetrahydrocortisol glucuronide levels 8,182 European ancestry individuals NA Affymetrix [15428145] (imputed) 4 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200267 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-2-aminoadipate levels 7,606 European ancestry individuals NA Affymetrix [15406230] (imputed) 1 blood N-acetyl-2-aminoadipate measurement http://www.ebi.ac.uk/efo/EFO_0022202 GCST90200268 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C17H20N2O5 (1) levels 8,252 European ancestry individuals NA Affymetrix [15430726] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200269 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (1) levels 7,487 European ancestry individuals NA Affymetrix [15397242] (imputed) 0 2-methoxyhydroquinone sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801061 GCST90200270 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylglutamine levels 8,128 European ancestry individuals NA Affymetrix [15425917] (imputed) 2 hexanoylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800262 GCST90199833 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylalanine levels 7,518 European ancestry individuals NA Affymetrix [15403446] (imputed) 0 gamma-glutamylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800675 GCST90199834 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3beta,17beta-diol disulfate levels 8,199 European ancestry individuals NA Affymetrix [15429186] (imputed) 5 5alpha-androstan-3beta,17beta-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0021115 GCST90199835 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methylproline levels 8,299 European ancestry individuals NA Affymetrix [15432359] (imputed) 0 N-methylproline measurement http://www.ebi.ac.uk/efo/EFO_0800039 GCST90199836 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carotenoid levels (cryptoxanthin) 8,226 European ancestry individuals NA Affymetrix [15430545] (imputed) 0 cryptoxanthin measurement http://www.ebi.ac.uk/efo/EFO_0007897 GCST90199837 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-pregnan-3beta,20alpha-diol disulfate levels 8,130 European ancestry individuals NA Affymetrix [15426253] (imputed) 3 5alpha-pregnan-diol disulfate measurement http://www.ebi.ac.uk/efo/EFO_0800286 GCST90199838 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholenate sulfate levels 8,249 European ancestry individuals NA Affymetrix [15430558] (imputed) 6 taurocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800277 GCST90199839 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnenediol disulfate (C21H34O8S2) levels 8,245 European ancestry individuals NA Affymetrix [15430325] (imputed) 5 pregnenediol disulfate (C21H34O8S2) measurement http://www.ebi.ac.uk/efo/EFO_0800279 GCST90199840 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholenate sulfate levels 8,250 European ancestry individuals NA Affymetrix [15431008] (imputed) 5 glycocholenate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800276 GCST90199841 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Androstenediol (3beta,17beta) disulfate (1) levels 8,222 European ancestry individuals NA Affymetrix [15429865] (imputed) 2 androstenediol (3beta,17beta) disulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800278 GCST90199842 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linoleate (20:2n6) levels 8,284 European ancestry individuals NA Affymetrix [15431817] (imputed) 0 dihomo-linoleate 20:2n6 measurement http://www.ebi.ac.uk/efo/EFO_0021064 GCST90200320 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cholate levels 7,892 European ancestry individuals NA Affymetrix [15419256] (imputed) 0 cholate measurement http://www.ebi.ac.uk/efo/EFO_0021509 GCST90200321 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-hydroxyisovalerate levels 8,201 European ancestry individuals NA Affymetrix [15429390] (imputed) 4 beta-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800125 GCST90200322 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Creatine levels 8,285 European ancestry individuals NA Affymetrix [15431847] (imputed) 2 creatine measurement http://www.ebi.ac.uk/efo/EFO_0010472 GCST90200323 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Anthranilate levels 5,773 European ancestry individuals NA Affymetrix [15303573] (imputed) 0 anthranilate measurement http://www.ebi.ac.uk/efo/EFO_0800123 GCST90200324 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerol levels 8,285 European ancestry individuals NA Affymetrix [15431588] (imputed) 0 glycerol measurement http://www.ebi.ac.uk/efo/EFO_0010115 GCST90200325 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylleucine levels 8,041 European ancestry individuals NA Affymetrix [15425086] (imputed) 0 gamma-glutamylleucine measurement http://www.ebi.ac.uk/efo/EFO_0021140 GCST90200326 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Choline levels 8,262 European ancestry individuals NA Affymetrix [15431074] (imputed) 1 choline measurement http://www.ebi.ac.uk/efo/EFO_0010116 GCST90200327 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxytyrosine levels 8,258 European ancestry individuals NA Affymetrix [15431547] (imputed) 6 3-methoxytyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021009 GCST90200328 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-phosphoglycerate levels 8,196 European ancestry individuals NA Affymetrix [15429091] (imputed) 0 3-phosphoglycerate measurement http://www.ebi.ac.uk/efo/EFO_0800152 GCST90200329 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-gpc (16:0/18:2) levels 8,230 European ancestry individuals NA Affymetrix [15430562] (imputed) 2 1-palmitoyl-2-linoleoyl-GPC (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800610 GCST90200330 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) levels 8,262 European ancestry individuals NA Affymetrix [15430799] (imputed) 7 1-palmitoyl-2-oleoyl-GPE (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800608 GCST90200331 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) levels 8,115 European ancestry individuals NA Affymetrix [15426269] (imputed) 2 1-palmitoyl-2-linoleoyl-GPI (16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800609 GCST90200332 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurocholic acid levels 7,743 European ancestry individuals NA Affymetrix [15410203] (imputed) 0 taurocholate measurement http://www.ebi.ac.uk/efo/EFO_0010538 GCST90200333 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurodeoxycholate levels 7,287 European ancestry individuals NA Affymetrix [15391666] (imputed) 0 taurodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010539 GCST90200334 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N4-acetylcytidine levels 7,425 European ancestry individuals NA Affymetrix [15398992] (imputed) 5 N4-acetylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800628 GCST90199758 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolebutyrate levels 4,423 European ancestry individuals NA Affymetrix [15434144] (imputed) 2 3-Indolebutyric acid measurement http://www.ebi.ac.uk/efo/EFO_0021559 GCST90199759 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-acetylamino-6-amino-3-methyluracil levels 8,006 European ancestry individuals NA Affymetrix [15422816] (imputed) 2 5-acetylamino-6-amino-3-methyluracil measurement http://www.ebi.ac.uk/efo/EFO_0800951 GCST90199760 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N1-methylinosine levels 8,147 European ancestry individuals NA Affymetrix [15425100] (imputed) 0 N1-methylinosine measurement http://www.ebi.ac.uk/efo/EFO_0800627 GCST90199761 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-carbamoylthreonyladenosine levels 8,176 European ancestry individuals NA Affymetrix [15429298] (imputed) 1 N6-carbamoylthreonyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0800629 GCST90199762 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methylxanthine levels 7,959 European ancestry individuals NA Affymetrix [15419806] (imputed) 3 1-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021174 GCST90199763 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,n2-dimethylguanosine levels 8,210 European ancestry individuals NA Affymetrix [15429417] (imputed) 0 N2,N2-dimethylguanosine measurement http://www.ebi.ac.uk/efo/EFO_0021125 GCST90199764 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyhippurate levels 8,259 European ancestry individuals NA Affymetrix [15431248] (imputed) 0 4-hydroxyhippurate measurement http://www.ebi.ac.uk/efo/EFO_0021508 GCST90199765 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-amino-3-carboxypropyl)uridine levels 7,679 European ancestry individuals NA Affymetrix [15408525] (imputed) 0 3-(3-amino-3-carboxypropyl)uridine measurement http://www.ebi.ac.uk/efo/EFO_0800632 GCST90199766 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5,6-dihydrouridine levels 8,210 European ancestry individuals NA Affymetrix [15430360] (imputed) 3 5,6-dihydrouridine measurement http://www.ebi.ac.uk/efo/EFO_0800631 GCST90199767 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylglutamine levels 8,251 European ancestry individuals NA Affymetrix [15430100] (imputed) 0 phenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021013 GCST90199768 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxydodecanedioate levels 7,168 European ancestry individuals NA Affymetrix [15386702] (imputed) 0 3-hydroxydodecanedioate measurement http://www.ebi.ac.uk/efo/EFO_0800226 GCST90199769 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-arachidonylglycerol (20:4) levels 7,650 European ancestry individuals NA Affymetrix [15405138] (imputed) 1 1-arachidonylglycerol (20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800224 GCST90199770 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylguanine levels 8,239 European ancestry individuals NA Affymetrix [15431182] (imputed) 1 7-methylguanine measurement http://www.ebi.ac.uk/efo/EFO_0021123 GCST90199771 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPE (18:0) levels 8,270 European ancestry individuals NA Affymetrix [15431209] (imputed) 4 1-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800227 GCST90199772 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol sulfate levels 8,249 European ancestry individuals NA Affymetrix [15431288] (imputed) 0 phenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021011 GCST90199773 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcarnitine levels 8,260 European ancestry individuals NA Affymetrix [15430785] (imputed) 2 oleoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021043 GCST90199774 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylisoleucine levels 8,267 European ancestry individuals NA Affymetrix [15431848] (imputed) 0 gamma-glutamylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0021139 GCST90199775 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Malonylcarnitine levels 5,822 European ancestry individuals NA Affymetrix [15307020] (imputed) 0 malonylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800232 GCST90199776 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoyl-GPC (16:1) levels 8,227 European ancestry individuals NA Affymetrix [15430107] (imputed) 3 1-palmitoleoyl-GPC (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800231 GCST90199777 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyl-2-pyridone-5-carboxamide levels 8,177 European ancestry individuals NA Affymetrix [15429353] (imputed) 0 n-methyl-2-pyridone-5-carboxamide measurement http://www.ebi.ac.uk/efo/EFO_0010994 GCST90199778 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-2-aminobutyrate levels 7,826 European ancestry individuals NA Affymetrix [15415623] (imputed) 0 gamma-glutamyl-2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800674 GCST90199779 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-GPG (18:0) levels 6,806 European ancestry individuals NA Affymetrix [15369548] (imputed) 2 1-stearoyl-GPG (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800228 GCST90199780 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexanoylglycine levels 6,015 European ancestry individuals NA Affymetrix [15320808] (imputed) 3 hexanoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800233 GCST90199781 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glutamine degradant levels 8,293 European ancestry individuals NA Affymetrix [15432089] (imputed) 5 glutamine measurement http://www.ebi.ac.uk/efo/EFO_0009768 GCST90199782 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerophosphoethanolamine levels 8,231 European ancestry individuals NA Affymetrix [15430230] (imputed) 1 glycerophosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800253 GCST90199808 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurolithocholate 3-sulfate levels 8,124 European ancestry individuals NA Affymetrix [15426475] (imputed) 2 taurolithocholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021036 GCST90199809 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPI (16:0) levels 8,246 European ancestry individuals NA Affymetrix [15429953] (imputed) 0 1-palmitoyl-GPI (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800257 GCST90199810 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycolithocholate sulfate levels 8,165 European ancestry individuals NA Affymetrix [15427926] (imputed) 2 glycolithocholate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800258 GCST90199811 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-hydroxyphenyl)propionate levels 7,304 European ancestry individuals NA Affymetrix [15393079] (imputed) 0 3-(3-hydroxyphenyl)propionate measurement http://www.ebi.ac.uk/efo/EFO_0800952 GCST90199812 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Deoxycarnitine levels 8,271 European ancestry individuals NA Affymetrix [15431333] (imputed) 4 deoxycarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800259 GCST90199813 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxycaproate levels 5,169 European ancestry individuals NA Affymetrix [15254609] (imputed) 0 alpha-hydroxycaproate measurement http://www.ebi.ac.uk/efo/EFO_0800261 GCST90199814 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-ribosyl-imidazoleacetate levels 8,205 European ancestry individuals NA Affymetrix [15428278] (imputed) 3 1-ribosyl-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800034 GCST90199815 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,4-dihydroxybutyrate levels 8,142 European ancestry individuals NA Affymetrix [15426237] (imputed) 1 blood 3,4-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022215 GCST90199816 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indoleacetylglutamine levels 6,161 European ancestry individuals NA Affymetrix [15333169] (imputed) 4 indoleacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800035 GCST90199817 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannitol/sorbitol levels 8,211 European ancestry individuals NA Affymetrix [15429432] (imputed) 0 sorbitol measurement http://www.ebi.ac.uk/efo/EFO_0010533 GCST90199818 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tryptophan betaine levels 8,216 European ancestry individuals NA Affymetrix [15429826] (imputed) 2 tryptophan betaine measurement http://www.ebi.ac.uk/efo/EFO_0021017 GCST90199819 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenate (20:3n3 or n6) levels 8,273 European ancestry individuals NA Affymetrix [15431551] (imputed) 1 dihomo-linolenate 20:3n3 or n6 measurement http://www.ebi.ac.uk/efo/EFO_0021046 GCST90199820 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPI (18:2) levels 8,268 European ancestry individuals NA Affymetrix [15431346] (imputed) 3 1-linoleoyl-GPI (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800266 GCST90199821 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPI (18:1) levels 8,252 European ancestry individuals NA Affymetrix [15430412] (imputed) 1 1-oleoyl-GPI (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800265 GCST90199822 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-cresol sulfate levels 7,315 European ancestry individuals NA Affymetrix [15394885] (imputed) 0 O-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800955 GCST90199823 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylphenol sulfate levels 8,280 European ancestry individuals NA Affymetrix [15431687] (imputed) 0 4-vinylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021149 GCST90199824 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pyrraline levels 7,920 European ancestry individuals NA Affymetrix [15418168] (imputed) 0 pyrraline measurement http://www.ebi.ac.uk/efo/EFO_0800954 GCST90199825 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-acetyllysine levels 8,242 European ancestry individuals NA Affymetrix [15430891] (imputed) 2 N6-acetyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800036 GCST90199826 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thymol sulfate levels 8,063 European ancestry individuals NA Affymetrix [15425707] (imputed) 2 thymol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021170 GCST90199827 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylserine levels 8,217 European ancestry individuals NA Affymetrix [15429926] (imputed) 1 N-acetylserine measurement http://www.ebi.ac.uk/efo/EFO_0800038 GCST90199828 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyladipate levels 6,958 European ancestry individuals NA Affymetrix [15370715] (imputed) 0 3-methyladipate measurement http://www.ebi.ac.uk/efo/EFO_0800263 GCST90199829 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-ethylphenylsulfate levels 8,139 European ancestry individuals NA Affymetrix [15426298] (imputed) 0 4-ethylphenylsulfate measurement http://www.ebi.ac.uk/efo/EFO_0021148 GCST90199830 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPE (18:0/18:1) levels 8,273 European ancestry individuals NA Affymetrix [15430613] (imputed) 4 1-stearoyl-2-oleoyl-GPE (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800269 GCST90199831 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethylarginine (sdma + adma) levels 8,233 European ancestry individuals NA Affymetrix [15430885] (imputed) 2 dimethylarginine (SDMA + ADMA) measurement http://www.ebi.ac.uk/efo/EFO_0800037 GCST90199832 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl indole-3-acetate levels 7,032 European ancestry individuals NA Affymetrix [15380209] (imputed) 0 methyl indole-3-acetate measurement http://www.ebi.ac.uk/efo/EFO_0801063 GCST90200296 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ursodeoxycholate levels 6,206 European ancestry individuals NA Affymetrix [15334066] (imputed) 0 ursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010547 GCST90200297 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-3-methylglutarate levels 8,073 European ancestry individuals NA Affymetrix [15425610] (imputed) 0 3-hydroxy-3-methylglutarate measurement http://www.ebi.ac.uk/efo/EFO_0800602 GCST90200298 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl ethanolamide levels 8,243 European ancestry individuals NA Affymetrix [15430106] (imputed) 1 oleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800604 GCST90200299 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylpyruvate levels 7,813 European ancestry individuals NA Affymetrix [15415430] (imputed) 1 4-hydroxyphenylpyruvate measurement http://www.ebi.ac.uk/efo/EFO_0800120 GCST90200300 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglutamine levels 8,217 European ancestry individuals NA Affymetrix [15428726] (imputed) 2 gamma-glutamylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0021138 GCST90200301 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-tocopherol levels 8,192 European ancestry individuals NA Affymetrix [15428650] (imputed) 0 alpha-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0007898 GCST90200302 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-alanine levels 8,220 European ancestry individuals NA Affymetrix [15430569] (imputed) 1 N-acetylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800118 GCST90200303 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citrate levels 8,260 European ancestry individuals NA Affymetrix [15430477] (imputed) 4 citrate measurement http://www.ebi.ac.uk/efo/EFO_0010114 GCST90200304 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminobutyrate levels 8,242 European ancestry individuals NA Affymetrix [15430647] (imputed) 2 2-aminobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0020017 GCST90200305 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Butyrate/isobutyrate (4:0) levels 8,004 European ancestry individuals NA Affymetrix [15422693] (imputed) 1 isobutyrate (4:0) measurement http://www.ebi.ac.uk/efo/EFO_0800605 GCST90200306 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Urate levels 8,264 European ancestry individuals NA Affymetrix [15430914] (imputed) 2 urate measurement http://www.ebi.ac.uk/efo/EFO_0004531 GCST90200307 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyisobutyrate levels 8,177 European ancestry individuals NA Affymetrix [15427851] (imputed) 0 3-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010983 GCST90200308 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillylmandelate (VMA) levels 8,216 European ancestry individuals NA Affymetrix [15429240] (imputed) 1 vanillylmandelate (VMA) measurement http://www.ebi.ac.uk/efo/EFO_0800119 GCST90200309 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-aminoisobutyrate levels 8,265 European ancestry individuals NA Affymetrix [15430478] (imputed) 7 3-aminoisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010980 GCST90200310 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetamidobutanoate levels 8,154 European ancestry individuals NA Affymetrix [15428044] (imputed) 2 4-acetamidobutanoate measurement http://www.ebi.ac.uk/efo/EFO_0021003 GCST90200311 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxystearate levels 8,241 European ancestry individuals NA Affymetrix [15428796] (imputed) 0 2-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0021059 GCST90200312 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N1-methyladenosine levels 8,247 European ancestry individuals NA Affymetrix [15430936] (imputed) 1 N1-methyladenosine measurement http://www.ebi.ac.uk/efo/EFO_0021122 GCST90200313 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylneuraminate levels 8,200 European ancestry individuals NA Affymetrix [15429999] (imputed) 1 N-acetylneuraminate measurement http://www.ebi.ac.uk/efo/EFO_0020022 GCST90200314 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylhistidine levels 8,220 European ancestry individuals NA Affymetrix [15429431] (imputed) 0 gamma-glutamylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800691 GCST90200315 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosaminylasparagine levels 8,144 European ancestry individuals NA Affymetrix [15427396] (imputed) 5 N-acetylglucosaminylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0800151 GCST90200316 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Homovanillate (hva) levels 6,320 European ancestry individuals NA Affymetrix [15343584] (imputed) 0 HVA measurement http://www.ebi.ac.uk/efo/EFO_0005131 GCST90200317 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acetoacetate levels 6,883 European ancestry individuals NA Affymetrix [15371190] (imputed) 0 acetoacetate measurement http://www.ebi.ac.uk/efo/EFO_0010111 GCST90200318 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cys-gly, oxidized levels 8,256 European ancestry individuals NA Affymetrix [15430969] (imputed) 4 cys-gly, oxidized measurement http://www.ebi.ac.uk/efo/EFO_0800122 GCST90200319 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-gpc (18:0) levels 8,240 European ancestry individuals NA Affymetrix [15430765] (imputed) 2 1-stearoyl-GPC (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800217 GCST90199732 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoyl sphingomyelin (d18:1/18:0) levels 8,258 European ancestry individuals NA Affymetrix [15431322] (imputed) 3 stearoyl sphingomyelin (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800611 GCST90200335 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/16:0) levels 8,266 European ancestry individuals NA Affymetrix [15431335] (imputed) 0 N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800607 GCST90200336 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurochenodeoxycholate levels 8,048 European ancestry individuals NA Affymetrix [15422810] (imputed) 0 taurochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010537 GCST90200337 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetate levels 7,906 European ancestry individuals NA Affymetrix [15417055] (imputed) 0 4-hydroxyphenylacetate measurement http://www.ebi.ac.uk/efo/EFO_0800124 GCST90200338 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5,6-dihydrothymine levels 8,219 European ancestry individuals NA Affymetrix [15429211] (imputed) 1 5,6-dihydrothymine measurement http://www.ebi.ac.uk/efo/EFO_0800638 GCST90200339 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-gpc (16:0/18:1) levels 8,249 European ancestry individuals NA Affymetrix [15430745] (imputed) 0 1-palmitoyl-2-oleoyl-GPC (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800612 GCST90200340 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingosine (d18:1/18:0) levels 8,254 European ancestry individuals NA Affymetrix [15430228] (imputed) 3 N-stearoyl-sphingosine (d18:1/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800613 GCST90200341 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate levels 8,164 European ancestry individuals NA Affymetrix [15427263] (imputed) 0 glycochenodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0010490 GCST90200342 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylmethionine levels 8,235 European ancestry individuals NA Affymetrix [15430719] (imputed) 1 N-formylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0800128 GCST90200343 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6,n6,n6-trimethyllysine levels 8,180 European ancestry individuals NA Affymetrix [15428764] (imputed) 3 N6,N6,N6-trimethyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800126 GCST90200344 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-adenosylhomocysteine (SAH) levels 6,142 European ancestry individuals NA Affymetrix [15326413] (imputed) 1 S-adenosylhomocysteine measurement http://www.ebi.ac.uk/efo/EFO_0010531 GCST90200345 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-acetaminophen sulfate levels 4,197 European ancestry individuals NA Affymetrix [15427876] (imputed) 0 4-acetaminophen sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021156 GCST90200346 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxyhippurate (salicylurate) levels 8,244 European ancestry individuals NA Affymetrix [15430686] (imputed) 0 salicylurate measurement http://www.ebi.ac.uk/efo/EFO_0010532 GCST90200347 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Quinolinate levels 8,203 European ancestry individuals NA Affymetrix [15429152] (imputed) 3 quinolinate measurement http://www.ebi.ac.uk/efo/EFO_0800175 GCST90200348 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosapentaenoate (EPA; 20:5n3) levels 8,257 European ancestry individuals NA Affymetrix [15430954] (imputed) 1 eicosapentaenoate (EPA; 20:5n3) measurement http://www.ebi.ac.uk/efo/EFO_0800616 GCST90200349 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Laurate (12:0) levels 8,226 European ancestry individuals NA Affymetrix [15430188] (imputed) 0 laurate 12:0 measurement http://www.ebi.ac.uk/efo/EFO_0021105 GCST90200350 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylputrescine levels 8,243 European ancestry individuals NA Affymetrix [15430104] (imputed) 3 N-acetylputrescine measurement http://www.ebi.ac.uk/efo/EFO_0800127 GCST90200351 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinate levels 7,965 European ancestry individuals NA Affymetrix [15419559] (imputed) 1 methylsuccinate measurement http://www.ebi.ac.uk/efo/EFO_0800129 GCST90200352 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9,10-DiHOME levels 7,557 European ancestry individuals NA Affymetrix [15405104] (imputed) 0 obsolete_9,10-dihome measurement http://www.ebi.ac.uk/efo/EFO_0021572 GCST90200353 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleate (18:2n6) levels 8,260 European ancestry individuals NA Affymetrix [15431169] (imputed) 0 linoleate (18:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800614 GCST90200354 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-diphosphate (ADP) levels 4,607 European ancestry individuals NA Affymetrix [15444084] (imputed) 0 adenosine diphosphate measurement http://www.ebi.ac.uk/efo/EFO_0010452 GCST90200355 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 5'-monophosphate (AMP) levels 8,218 European ancestry individuals NA Affymetrix [15430189] (imputed) 0 Adenosine 5'-monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0021574 GCST90200356 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adenosine 3',5'-cyclic monophosphate (camp) levels 6,756 European ancestry individuals NA Affymetrix [15362708] (imputed) 2 cyclic adenosine monophosphate measurement http://www.ebi.ac.uk/efo/EFO_0010473 GCST90200357 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonate (20:4n6) levels 8,272 European ancestry individuals NA Affymetrix [15431405] (imputed) 1 arachidonate 20:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021063 GCST90200358 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-methylthioadenosine (mta) levels 8,210 European ancestry individuals NA Affymetrix [15429790] (imputed) 3 5-methylthioadenosine (MTA) measurement http://www.ebi.ac.uk/efo/EFO_0800130 GCST90200359 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPC (16:0) levels 8,232 European ancestry individuals NA Affymetrix [15430245] (imputed) 1 1-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800214 GCST90199733 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hyocholate levels 5,782 European ancestry individuals NA Affymetrix [15307258] (imputed) 0 hyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800219 GCST90199734 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylhistidine levels 7,054 European ancestry individuals NA Affymetrix [15378724] (imputed) 4 N-acetylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800022 GCST90199735 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alpha-hydroxyisovalerate levels 8,208 European ancestry individuals NA Affymetrix [15429530] (imputed) 5 alpha-hydroxyisovalerate measurement http://www.ebi.ac.uk/efo/EFO_0800023 GCST90199736 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylproline levels 7,100 European ancestry individuals NA Affymetrix [15377687] (imputed) 1 blood N-acetylproline measurement http://www.ebi.ac.uk/efo/EFO_0022207 GCST90199737 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stachydrine levels 8,297 European ancestry individuals NA Affymetrix [15432365] (imputed) 0 stachydrine measurement http://www.ebi.ac.uk/efo/EFO_0021169 GCST90199738 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicyluric glucuronide levels 5,190 European ancestry individuals NA Affymetrix [15246649] (imputed) 0 salicyluric glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0021162 GCST90199739 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol sulfate levels 8,183 European ancestry individuals NA Affymetrix [15426685] (imputed) 0 p-cresol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0010998 GCST90199740 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylglycine levels 8,263 European ancestry individuals NA Affymetrix [15431301] (imputed) 2 gamma-glutamylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800670 GCST90199741 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-gpc (18:2) levels 8,262 European ancestry individuals NA Affymetrix [15431252] (imputed) 2 1-linoleoyl-GPC (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800223 GCST90199742 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcarnitine levels 8,133 European ancestry individuals NA Affymetrix [15425275] (imputed) 3 stearoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021045 GCST90199743 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenoate (20:1) levels 8,277 European ancestry individuals NA Affymetrix [15431781] (imputed) 0 eicosenoate (20:1) measurement http://www.ebi.ac.uk/efo/EFO_0800220 GCST90199744 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Aconitate [cis or trans] levels 8,262 European ancestry individuals NA Affymetrix [15431438] (imputed) 0 aconitate measurement http://www.ebi.ac.uk/efo/EFO_0010451 GCST90199745 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erythronate levels 8,198 European ancestry individuals NA Affymetrix [15430299] (imputed) 1 erythronate measurement http://www.ebi.ac.uk/efo/EFO_0021025 GCST90199746 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Isovalerylcarnitine (C5) levels 8,266 European ancestry individuals NA Affymetrix [15430948] (imputed) 2 isovalerylcarnitine (C5) measurement http://www.ebi.ac.uk/efo/EFO_0800024 GCST90199747 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linolenate [alpha or gamma; (18:3n3 or 6)] levels 8,257 European ancestry individuals NA Affymetrix [15430765] (imputed) 0 linolenate [alpha or gamma; 18:3n3 or 6] measurement http://www.ebi.ac.uk/efo/EFO_0021050 GCST90199748 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylthreonine levels 8,231 European ancestry individuals NA Affymetrix [15429697] (imputed) 1 gamma-glutamylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0021143 GCST90199749 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Laurylcarnitine levels 8,241 European ancestry individuals NA Affymetrix [15430538] (imputed) 0 laurylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021041 GCST90199750 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamylmethionine levels 8,237 European ancestry individuals NA Affymetrix [15430690] (imputed) 0 gamma-glutamylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021141 GCST90199751 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Epiandrosterone sulfate levels 8,174 European ancestry individuals NA Affymetrix [15427681] (imputed) 4 epiandrosterone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0021120 GCST90199752 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltryptophan levels 7,902 European ancestry individuals NA Affymetrix [15418954] (imputed) 1 gamma-glutamyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0800671 GCST90199753 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 7-methylxanthine levels 8,019 European ancestry individuals NA Affymetrix [15423257] (imputed) 1 7-methylxanthine measurement http://www.ebi.ac.uk/efo/EFO_0021176 GCST90199754 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3,7-dimethylurate levels 6,894 European ancestry individuals NA Affymetrix [15365213] (imputed) 0 3,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0800949 GCST90199755 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,7-dimethyluric acid levels 7,950 European ancestry individuals NA Affymetrix [15421417] (imputed) 0 1,7-dimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021512 GCST90199756 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,3,7-trimethylurate levels 7,446 European ancestry individuals NA Affymetrix [15397812] (imputed) 1 1,3,7-trimethylurate measurement http://www.ebi.ac.uk/efo/EFO_0021172 GCST90199757 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (3) levels 7,970 European ancestry individuals NA Affymetrix [15421076] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200271 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (1) levels 8,245 European ancestry individuals NA Affymetrix [15429921] (imputed) 1 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200272 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyhydroquinone sulfate (2) levels 5,778 European ancestry individuals NA Affymetrix [15299234] (imputed) 0 2-methoxyhydroquinone sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801062 GCST90200273 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Cis-3,4-methyleneheptanoylglycine levels 8,106 European ancestry individuals NA Affymetrix [15424897] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200274 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (2) levels 8,252 European ancestry individuals NA Affymetrix [15429788] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200275 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,4-di-tert-butylphenol levels 8,251 European ancestry individuals NA Affymetrix [15428951] (imputed) 0 blood 2,4-di-tert-butylphenol measurement http://www.ebi.ac.uk/efo/EFO_0022221 GCST90200276 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Bilirubin degradation product, C16H18N2O5 (1) levels 7,864 European ancestry individuals NA Affymetrix [15416911] (imputed) 1 bilirubin measurement http://www.ebi.ac.uk/efo/EFO_0004570 GCST90200277 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyoctanoylcarnitine (2) levels 8,243 European ancestry individuals NA Affymetrix [15429862] (imputed) 3 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200278 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pantothenate levels 8,194 European ancestry individuals NA Affymetrix [15429176] (imputed) 0 pantothenate measurement http://www.ebi.ac.uk/efo/EFO_0021034 GCST90200279 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-oxoproline levels 8,247 European ancestry individuals NA Affymetrix [15431109] (imputed) 2 5-oxoproline measurement http://www.ebi.ac.uk/efo/EFO_0010988 GCST90200280 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phosphoethanolamine levels 8,253 European ancestry individuals NA Affymetrix [15431131] (imputed) 1 phosphoethanolamine measurement http://www.ebi.ac.uk/efo/EFO_0800600 GCST90200281 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Picolinate levels 7,051 European ancestry individuals NA Affymetrix [15378583] (imputed) 3 picolinate measurement http://www.ebi.ac.uk/efo/EFO_0800115 GCST90200282 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-ureidopropionate levels 7,543 European ancestry individuals NA Affymetrix [15400962] (imputed) 1 3-ureidopropionate measurement http://www.ebi.ac.uk/efo/EFO_0010641 GCST90200283 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Erucate (22:1n9) levels 8,208 European ancestry individuals NA Affymetrix [15430630] (imputed) 0 erucate (22:1n9) measurement http://www.ebi.ac.uk/efo/EFO_0800601 GCST90200284 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosenedioate (C20:1-DC) levels 8,166 European ancestry individuals NA Affymetrix [15429101] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90200285 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Allantoin levels 8,252 European ancestry individuals NA Affymetrix [15430636] (imputed) 0 allantoin measurement http://www.ebi.ac.uk/efo/EFO_0010456 GCST90200286 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylvaline levels 8,218 European ancestry individuals NA Affymetrix [15430092] (imputed) 0 N-acetylvaline measurement http://www.ebi.ac.uk/efo/EFO_0800117 GCST90200287 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylleucine levels 7,905 European ancestry individuals NA Affymetrix [15416611] (imputed) 1 N-acetylleucine measurement http://www.ebi.ac.uk/efo/EFO_0800116 GCST90200288 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylmethionine levels 7,993 European ancestry individuals NA Affymetrix [15421342] (imputed) 1 N-acetylmethionine measurement http://www.ebi.ac.uk/efo/EFO_0021427 GCST90200289 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycerate levels 8,222 European ancestry individuals NA Affymetrix [15429403] (imputed) 1 glycerate measurement http://www.ebi.ac.uk/efo/EFO_0021029 GCST90200290 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sarcosine levels 8,223 European ancestry individuals NA Affymetrix [15429708] (imputed) 0 Sarcosine measurement http://www.ebi.ac.uk/efo/EFO_0021668 GCST90200291 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans-4-hydroxyproline levels 8,252 European ancestry individuals NA Affymetrix [15430498] (imputed) 1 trans-4-hydroxyproline measurement http://www.ebi.ac.uk/efo/EFO_0800114 GCST90200292 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thyroxine levels 8,262 European ancestry individuals NA Affymetrix [15431006] (imputed) 1 thyroxine measurement http://www.ebi.ac.uk/efo/EFO_0005130 GCST90200293 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pipecolate levels 8,161 European ancestry individuals NA Affymetrix [15427570] (imputed) 0 pipecolate measurement http://www.ebi.ac.uk/efo/EFO_0021006 GCST90200294 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyltyrosine levels 8,221 European ancestry individuals NA Affymetrix [15430059] (imputed) 2 gamma-glutamyltyrosine measurement http://www.ebi.ac.uk/efo/EFO_0021144 GCST90200295 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23997 levels 89 South Asian ancestry individuals NA Affymetrix [4313829] (imputed) 0 X-23997 measurement http://www.ebi.ac.uk/efo/EFO_0800868 GCST90204021 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-23974 levels 102 South Asian ancestry individuals NA Affymetrix [4482413] (imputed) 0 X-23974 measurement http://www.ebi.ac.uk/efo/EFO_0800867 GCST90204022 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24328 levels 104 South Asian ancestry individuals NA Affymetrix [4447817] (imputed) 0 X-24328 measurement http://www.ebi.ac.uk/efo/EFO_0800873 GCST90204023 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24307 levels 107 South Asian ancestry individuals NA Affymetrix [4390367] (imputed) 0 X-24307 measurement http://www.ebi.ac.uk/efo/EFO_0800871 GCST90204024 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800453 GCST90201484 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPI (18:0/18:1) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 1-stearoyl-2-oleoyl-GPI (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800469 GCST90201485 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dilinoleoyl-GPE (18:2/18:2) levels 54 African ancestry individuals NA Affymetrix [7596777] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201486 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoylcholine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 oleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800477 GCST90201487 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoylcholine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 palmitoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800473 GCST90201488 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methylserine levels 58 African ancestry individuals NA Affymetrix [7523085] (imputed) 0 2-methylserine measurement http://www.ebi.ac.uk/efo/EFO_0800087 GCST90201489 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (p-18:0/18:2) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-(1-enyl-stearoyl)-2-linoleoyl-GPE (P-18:0/18:2)* measurement http://www.ebi.ac.uk/efo/EFO_0020014 GCST90201490 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate glucuronide (1) levels 59 African ancestry individuals NA Affymetrix [7488508] (imputed) 0 glycochenodeoxycholate glucuronide (1) measurement http://www.ebi.ac.uk/efo/EFO_0800474 GCST90201491 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (S)-3-hydroxybutyrylcarnitine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 (S)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800475 GCST90201492 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ascorbic acid 2-sulfate levels 57 African ancestry individuals NA Affymetrix [7550299] (imputed) 0 ascorbic acid 2-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800169 GCST90201493 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arachidonoylcholine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 arachidonoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800478 GCST90201494 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 1-linoleoyl-2-linolenoyl-GPC (18:2/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800483 GCST90201495 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) levels 55 African ancestry individuals NA Affymetrix [7658752] (imputed) 0 1-palmitoleoyl-2-linolenoyl-GPC (16:1/18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800484 GCST90201496 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 59 African ancestry individuals NA Affymetrix [7488508] (imputed) 0 glycosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800476 GCST90201497 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methylsuccinoylcarnitine levels 56 African ancestry individuals NA Affymetrix [7565950] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201498 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) levels 59 African ancestry individuals NA Affymetrix [7485526] (imputed) 0 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800470 GCST90201499 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-GPG (18:2) levels 59 African ancestry individuals NA Affymetrix [7488508] (imputed) 0 1-linoleoyl-GPG (18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800472 GCST90201500 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Furaneol sulfate levels 43 African ancestry individuals NA Affymetrix [7780834] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90201501 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihomo-linolenoyl-choline levels 51 African ancestry individuals NA Affymetrix [7754204] (imputed) 0 dihomo-linolenoyl-choline measurement http://www.ebi.ac.uk/efo/EFO_0800481 GCST90201502 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Caffeic acid sulfate levels 54 African ancestry individuals NA Affymetrix [7623921] (imputed) 0 caffeic acid sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801013 GCST90201503 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosahexaenoylcholine levels 55 African ancestry individuals NA Affymetrix [7599035] (imputed) 0 docosahexaenoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800479 GCST90201504 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetoylcarnitine levels 90 East Asian ancestry individuals NA Affymetrix [4353627] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202470 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nonanoylcarnitine (C9) levels 97 East Asian ancestry individuals NA Affymetrix [4236714] (imputed) 0 nonanoylcarnitine (C9) measurement http://www.ebi.ac.uk/efo/EFO_0800381 GCST90202471 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trans 3,4-methyleneheptanoate levels 88 East Asian ancestry individuals NA Affymetrix [4186111] (imputed) 0 3,4-methyleneheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0801011 GCST90202472 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tricosanoyl sphingomyelin (d18:1/23:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 tricosanoyl sphingomyelin (d18:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0800401 GCST90202473 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-gpc (18:0/22:6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-stearoyl-2-docosahexaenoyl-GPC (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800392 GCST90202474 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenol glucuronide levels 58 East Asian ancestry individuals NA Affymetrix [4156528] (imputed) 0 phenol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800084 GCST90202475 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-docosahexaenoyl-gpc (16:0/22:6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-palmitoyl-2-docosahexaenoyl-GPC (16:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800391 GCST90202476 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:1/17:0, d17:1/18:0, d19:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022107 GCST90202477 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-gpc (18:0/18:1) levels 103 East Asian ancestry individuals NA Affymetrix [4299391] (imputed) 0 1-stearoyl-2-oleoyl-GPC (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800389 GCST90202478 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl ethanolamide levels 100 East Asian ancestry individuals NA Affymetrix [4355624] (imputed) 0 linoleoyl ethanolamide measurement http://www.ebi.ac.uk/efo/EFO_0800387 GCST90202479 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleate/vaccenate (18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 vaccenate (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800397 GCST90202480 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxybutyrate/2-hydroxyisobutyrate levels 101 East Asian ancestry individuals NA Affymetrix [4333308] (imputed) 0 2-hydroxyisobutyrate measurement http://www.ebi.ac.uk/efo/EFO_0010979 GCST90202481 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-gpc (16:0/20:4n6) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPC (16:0/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800390 GCST90202482 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoyl dihydrosphingomyelin (d18:0/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 palmitoyl dihydrosphingomyelin (d18:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800400 GCST90202483 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycochenodeoxycholate 3-sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4295850] (imputed) 0 glycochenodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800384 GCST90202484 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoleoylglycerol (16:1) levels 83 East Asian ancestry individuals NA Affymetrix [4327593] (imputed) 0 1-palmitoleoylglycerol (16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800398 GCST90202485 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) levels 101 East Asian ancestry individuals NA Affymetrix [4334602] (imputed) 0 1-stearoyl-2-linoleoyl-GPI (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800413 GCST90202486 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (p-18:0/20:4) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-stearoyl)-2-arachidonoyl-GPE (P-18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800415 GCST90202487 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:2/23:0, d18:1/23:1, d17:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022116 GCST90202488 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) levels 103 East Asian ancestry individuals NA Affymetrix [4300066] (imputed) 0 1-stearoyl-2-arachidonoyl-GPE (18:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800403 GCST90202489 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/24:1, d18:1/24:2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:2/24:1, d18:1/24:2) measurement http://www.ebi.ac.uk/efo/EFO_0022117 GCST90202490 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-linoleoyl-gpc (18:0/18:2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-stearoyl-2-linoleoyl-GPC (18:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800404 GCST90202491 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-palmitoleoyl-gpc (16:0/16:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-palmitoyl-2-palmitoleoyl-GPC(16:0/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800406 GCST90202492 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:0/18:0, d19:0/17:0) levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202493 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl dihydrosphingomyelin (d18:0/22:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 behenoyl dihydrosphingomyelin (d18:0/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800427 GCST90202494 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:1/21:0, d17:1/22:0, d16:1/23:0) measurement http://www.ebi.ac.uk/efo/EFO_0022111 GCST90202495 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 1-palmitoyl-2-dihomo-linolenoyl-GPC (16:0/20:3n3 or 6) measurement http://www.ebi.ac.uk/efo/EFO_0800407 GCST90202496 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 lactosyl-N-palmitoyl-sphingosine (d18:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800429 GCST90202497 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-arachidonoyl-gpc (p-16:0/20:4) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPC (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800423 GCST90202498 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) levels 101 East Asian ancestry individuals NA Affymetrix [4333686] (imputed) 0 1-palmitoyl-2-arachidonoyl-GPI (16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800412 GCST90202499 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-tocopherol/beta-tocopherol levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 beta-tocopherol measurement http://www.ebi.ac.uk/efo/EFO_0800168 GCST90202500 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (p-16:0/20:4) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-palmitoyl)-2-arachidonoyl-GPE (P-16:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800417 GCST90202501 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (p-16:0/18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-palmitoyl)-2-oleoyl-GPE (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800419 GCST90202502 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) levels 103 East Asian ancestry individuals NA Affymetrix [4298993] (imputed) 0 1-stearoyl-2-docosahexaenoyl-GPE (18:0/22:6) measurement http://www.ebi.ac.uk/efo/EFO_0800411 GCST90202503 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (p-16:0/18:2) levels 103 East Asian ancestry individuals NA Affymetrix [4300867] (imputed) 0 1-(1-enyl-palmitoyl)-2-linoleoyl-GPC (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800422 GCST90202504 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-oleoyl-gpc (p-16:0/18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-palmitoyl)-2-oleoyl-GPC (P-16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800420 GCST90202505 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-stearoyl-2-oleoyl-GPI (18:0/18:1) levels 101 East Asian ancestry individuals NA Affymetrix [4338382] (imputed) 0 1-stearoyl-2-oleoyl-GPI (18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800469 GCST90202506 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) levels 103 East Asian ancestry individuals NA Affymetrix [4301539] (imputed) 0 1-palmitoyl-2-oleoyl-GPI (16:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800439 GCST90202507 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methylserine levels 100 East Asian ancestry individuals NA Affymetrix [4347451] (imputed) 0 2-methylserine measurement http://www.ebi.ac.uk/efo/EFO_0800087 GCST90202508 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (p-16:0/18:2) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-palmitoyl)-2-linoleoyl-GPE (P-16:0/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800440 GCST90202509 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5-hydroxyindole sulfate levels 76 East Asian ancestry individuals NA Affymetrix [4257978] (imputed) 0 5-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800085 GCST90202510 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Myristoyl dihydrosphingomyelin (d18:0/14:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 myristoyl dihydrosphingomyelin (d18:0/14:0) measurement http://www.ebi.ac.uk/efo/EFO_0800433 GCST90202511 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-myristoyl-2-arachidonoyl-GPC (14:0/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800453 GCST90202512 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) levels 97 East Asian ancestry individuals NA Affymetrix [4226087] (imputed) 0 1-linoleoyl-2-arachidonoyl-GPC (18:2/20:4n6) measurement http://www.ebi.ac.uk/efo/EFO_0800450 GCST90202513 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-palmitoyl)-2-palmitoyl-GPC (P-16:0/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800466 GCST90202514 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2-dilinoleoyl-GPE (18:2/18:2) levels 92 East Asian ancestry individuals NA Affymetrix [4331961] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202515 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) levels 101 East Asian ancestry individuals NA Affymetrix [4331029] (imputed) 0 1-oleoyl-2-arachidonoyl-GPE (18:1/20:4) measurement http://www.ebi.ac.uk/efo/EFO_0800470 GCST90202516 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) levels 102 East Asian ancestry individuals NA Affymetrix [4320545] (imputed) 0 1-oleoyl-2-linoleoyl-GPE (18:1/18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800443 GCST90202517 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thioproline levels 103 East Asian ancestry individuals NA Affymetrix [4300331] (imputed) 0 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90202518 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycocholate glucuronide (1) levels 54 East Asian ancestry individuals NA Affymetrix [4280980] (imputed) 0 glycocholic acid measurement http://www.ebi.ac.uk/efo/EFO_0010492 GCST90202519 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hexadecadienoate (16:2n6) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 hexadecadienoate (16:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800491 GCST90201505 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Thioproline levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 thioproline measurement http://www.ebi.ac.uk/efo/EFO_0801012 GCST90201506 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Palmitoleoylcarnitine (C16:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 palmitoleoylcarnitine (C16:1) measurement http://www.ebi.ac.uk/efo/EFO_0800493 GCST90201507 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) levels 55 African ancestry individuals NA Affymetrix [7733633] (imputed) 0 pimeloylcarnitine/3-methyladipoylcarnitine (C7-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800494 GCST90201508 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxyphenylacetylglutamine levels 56 African ancestry individuals NA Affymetrix [7585145] (imputed) 0 4-hydroxyphenylacetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800688 GCST90201509 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methylcytidine levels 59 African ancestry individuals NA Affymetrix [7507469] (imputed) 0 2'-O-methylcytidine measurement http://www.ebi.ac.uk/efo/EFO_0800635 GCST90201510 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2,3-dihydroxy-2-methylbutyrate levels 59 African ancestry individuals NA Affymetrix [7496308] (imputed) 0 blood 2,3-dihydroxy-2-methylbutyrate measurement http://www.ebi.ac.uk/efo/EFO_0022219 GCST90201511 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2'-o-methyluridine levels 57 African ancestry individuals NA Affymetrix [7559649] (imputed) 0 2'-O-methyluridine measurement http://www.ebi.ac.uk/efo/EFO_0800636 GCST90201512 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-glutamyl-alpha-lysine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 gamma-glutamyl-alpha-lysine measurement http://www.ebi.ac.uk/efo/EFO_0800689 GCST90201513 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearoylcholine levels 54 African ancestry individuals NA Affymetrix [7593339] (imputed) 0 stearoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800534 GCST90201514 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl ceramide (d18:1/23:1, d17:1/24:1) levels 43 African ancestry individuals NA Affymetrix [7649196] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90201515 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/24:1) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 lactosyl-N-nervonoyl-sphingosine (d18:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0800517 GCST90201516 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-stearoyl-sphingadienine (d18:2/18:0) levels 49 African ancestry individuals NA Affymetrix [7350329] (imputed) 0 N-stearoyl-sphingadienine (d18:2/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800521 GCST90201517 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 glycosyl-N-behenoyl-sphingadienine (d18:2/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800520 GCST90201518 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/14:0, d16:1/16:0) levels 47 African ancestry individuals NA Affymetrix [7521122] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90201519 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ceramide (d18:1/17:0, d17:1/18:0) levels 41 African ancestry individuals NA Affymetrix [7581682] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90201520 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Perfluorooctanesulfonate (PFOS) levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 perfluorooctanesulfonate (PFOS) measurement http://www.ebi.ac.uk/efo/EFO_0801018 GCST90201521 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Nisinate (24:6n3) levels 40 African ancestry individuals NA Affymetrix [7635432] (imputed) 0 nisinate (24:6n3) measurement http://www.ebi.ac.uk/efo/EFO_0800536 GCST90201522 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoyl-heptadecasphingosine (d17:1/16:0) levels 50 African ancestry individuals NA Affymetrix [7309361] (imputed) 0 N-palmitoyl-heptadecasphingosine (d17:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800531 GCST90201523 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-oleoylserine levels 58 African ancestry individuals NA Affymetrix [7595847] (imputed) 0 N-oleoylserine measurement http://www.ebi.ac.uk/efo/EFO_0800525 GCST90201524 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) levels 59 African ancestry individuals NA Affymetrix [7497436] (imputed) 0 glycosyl-N-(2-hydroxynervonoyl)-sphingosine (d18:1/24:1(2OH)) measurement http://www.ebi.ac.uk/efo/EFO_0800533 GCST90201525 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoylcholine levels 60 African ancestry individuals NA Affymetrix [7469754] (imputed) 0 linoleoylcholine measurement http://www.ebi.ac.uk/efo/EFO_0800535 GCST90201526 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycosyl-N-tricosanoyl-sphingadienine (d18:2/23:0) levels 56 African ancestry individuals NA Affymetrix [7557157] (imputed) 0 ceramide measurement http://www.ebi.ac.uk/efo/EFO_0010222 GCST90201527 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] levels 56 African ancestry individuals NA Affymetrix [7552175] (imputed) 0 linoleoyl-arachidonoyl-glycerol (18:2/20:4) [1] measurement http://www.ebi.ac.uk/efo/EFO_0800499 GCST90201528 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2R,3R-dihydroxybutyrate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2R,3R-dihydroxybutyrate measurement http://www.ebi.ac.uk/efo/EFO_0800314 GCST90202344 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Acisoga levels 98 East Asian ancestry individuals NA Affymetrix [4214378] (imputed) 0 acisoga measurement http://www.ebi.ac.uk/efo/EFO_0800068 GCST90202395 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-oxopiperidine-2-carboxylate levels 102 East Asian ancestry individuals NA Affymetrix [4318837] (imputed) 0 6-oxopiperidine-2-carboxylate measurement http://www.ebi.ac.uk/efo/EFO_0800066 GCST90202396 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-delta-acetylornithine levels 102 East Asian ancestry individuals NA Affymetrix [4316527] (imputed) 0 N-delta-acetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800067 GCST90202397 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N2,N5-diacetylornithine levels 90 East Asian ancestry individuals NA Affymetrix [4364450] (imputed) 0 N2,N5-diacetylornithine measurement http://www.ebi.ac.uk/efo/EFO_0800070 GCST90202398 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminoheptanoate levels 103 East Asian ancestry individuals NA Affymetrix [4305995] (imputed) 0 2-aminoheptanoate measurement http://www.ebi.ac.uk/efo/EFO_0800352 GCST90202399 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxytyramine sulfate levels 71 East Asian ancestry individuals NA Affymetrix [4379641] (imputed) 0 3-methoxytyramine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800071 GCST90202400 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-allylcysteine levels 99 East Asian ancestry individuals NA Affymetrix [4188602] (imputed) 0 S-allylcysteine measurement http://www.ebi.ac.uk/efo/EFO_0800985 GCST90202401 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylalliin levels 84 East Asian ancestry individuals NA Affymetrix [4281261] (imputed) 0 N-acetylalliin measurement http://www.ebi.ac.uk/efo/EFO_0800987 GCST90202402 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Fructosyllysine levels 102 East Asian ancestry individuals NA Affymetrix [4317224] (imputed) 0 fructosyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800073 GCST90202403 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-oleoyl)-GPE (p-18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-oleoyl)-GPE (P-18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800359 GCST90202404 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-linolenoyl-GPC (18:3) levels 103 East Asian ancestry individuals NA Affymetrix [4299458] (imputed) 0 1-linolenoyl-GPC (18:3) measurement http://www.ebi.ac.uk/efo/EFO_0800354 GCST90202405 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminophenol sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4302350] (imputed) 0 2-aminophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800982 GCST90202406 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methionine sulfone levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 methionine sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800072 GCST90202407 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl glucopyranoside (alpha + beta) levels 103 East Asian ancestry individuals NA Affymetrix [4298892] (imputed) 0 methyl glucopyranoside (alpha + beta) measurement http://www.ebi.ac.uk/efo/EFO_0800991 GCST90202408 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-(3-hydroxyphenyl)propionate sulfate levels 75 East Asian ancestry individuals NA Affymetrix [4274083] (imputed) 0 3-(3-hydroxyphenyl)propionate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800990 GCST90202409 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Etiocholanolone glucuronide levels 99 East Asian ancestry individuals NA Affymetrix [4188925] (imputed) 0 etiocholanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800362 GCST90202410 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 17alpha-hydroxypregnanolone glucuronide levels 73 East Asian ancestry individuals NA Affymetrix [4300831] (imputed) 0 17alpha-hydroxypregnanolone glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800363 GCST90202411 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-oleoyl-GPG (18:1) levels 85 East Asian ancestry individuals NA Affymetrix [4252047] (imputed) 0 1-oleoyl-GPG (18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800366 GCST90202412 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/14:0, d18:1/14:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:2/14:0, d18:1/14:1) measurement http://www.ebi.ac.uk/efo/EFO_0022114 GCST90202413 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. O-sulfo-l-tyrosine levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90202414 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyltaurine levels 101 East Asian ancestry individuals NA Affymetrix [4330427] (imputed) 0 N-acetyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0020023 GCST90202415 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPG (16:0) levels 100 East Asian ancestry individuals NA Affymetrix [4358963] (imputed) 0 1-palmitoyl-GPG (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800367 GCST90202416 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methylglutarylcarnitine (2) levels 101 East Asian ancestry individuals NA Affymetrix [4334753] (imputed) 0 3-methylglutarylcarnitine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800074 GCST90202417 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ferulic acid 4-sulfate levels 92 East Asian ancestry individuals NA Affymetrix [4328197] (imputed) 0 ferulic acid 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800989 GCST90202418 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 9-hydroxystearate levels 90 East Asian ancestry individuals NA Affymetrix [4360970] (imputed) 0 9-hydroxystearate measurement http://www.ebi.ac.uk/efo/EFO_0800369 GCST90202419 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Phenylacetylcarnitine levels 99 East Asian ancestry individuals NA Affymetrix [4193933] (imputed) 0 phenylacetylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800686 GCST90202445 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Propyl 4-hydroxybenzoate sulfate levels 100 East Asian ancestry individuals NA Affymetrix [4356715] (imputed) 0 propyl 4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801005 GCST90202446 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1,2,3-benzenetriol sulfate (2) levels 93 East Asian ancestry individuals NA Affymetrix [4305449] (imputed) 0 1,2,3-benzenetriol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0801008 GCST90202447 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:1/22:1, d18:2/22:0, d16:1/24:1) measurement http://www.ebi.ac.uk/efo/EFO_0022112 GCST90202448 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/22:2, d18:2/22:1, d16:1/24:2) levels 103 East Asian ancestry individuals NA Affymetrix [4299732] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202449 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-carbamoylalanine levels 79 East Asian ancestry individuals NA Affymetrix [4187313] (imputed) 0 blood N-carbamoylalanine measurement http://www.ebi.ac.uk/efo/EFO_0022203 GCST90202450 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 4-sulfate levels 76 East Asian ancestry individuals NA Affymetrix [4250846] (imputed) 0 dopamine 4-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800081 GCST90202451 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:2, d18:2/20:1, d16:1/22:2) levels 102 East Asian ancestry individuals NA Affymetrix [4316033] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202452 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3beta-hydroxy-5-cholestenoate levels 103 East Asian ancestry individuals NA Affymetrix [4300329] (imputed) 0 3beta-hydroxy-5-cholestenoate measurement http://www.ebi.ac.uk/efo/EFO_0800379 GCST90202453 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lignoceroyl sphingomyelin (d18:1/24:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 lignoceroyl sphingomyelin (d18:1/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800377 GCST90202454 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adipoylcarnitine (C6-DC) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 adipoylcarnitine (C6-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800380 GCST90202455 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dopamine 3-o-sulfate levels 103 East Asian ancestry individuals NA Affymetrix [4300748] (imputed) 0 dopamine 3-O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800082 GCST90202456 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Behenoyl sphingomyelin (d18:1/22:0) levels 103 East Asian ancestry individuals NA Affymetrix [4302794] (imputed) 0 behenoyl sphingomyelin (d18:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0800376 GCST90202457 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d17:1/16:0, d18:1/15:0, d16:1/17:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 sphingomyelin measurement http://www.ebi.ac.uk/efo/EFO_0010118 GCST90202458 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. C-glycosyltryptophan levels 102 East Asian ancestry individuals NA Affymetrix [4317062] (imputed) 0 C-glycosyltryptophan measurement http://www.ebi.ac.uk/efo/EFO_0021014 GCST90202459 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methoxycatechol sulfate (1) levels 103 East Asian ancestry individuals NA Affymetrix [4300473] (imputed) 0 3-methoxycatechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0801009 GCST90202460 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabitol/xylitol levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 arabitol measurement http://www.ebi.ac.uk/efo/EFO_0800148 GCST90202461 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxyhexanoate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-hydroxyhexanoate measurement http://www.ebi.ac.uk/efo/EFO_0800378 GCST90202462 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylglucosamine/n-acetylgalactosamine levels 100 East Asian ancestry individuals NA Affymetrix [4353924] (imputed) 0 N-acetylgalactosamine measurement http://www.ebi.ac.uk/efo/EFO_0800149 GCST90202463 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Citraconate/glutaconate levels 100 East Asian ancestry individuals NA Affymetrix [4351733] (imputed) 0 blood glutaconic acid measurement, blood Citraconic acid measurement http://www.ebi.ac.uk/efo/EFO_0022200, http://www.ebi.ac.uk/efo/EFO_0022201 GCST90202464 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylkynurenine (2) levels 80 East Asian ancestry individuals NA Affymetrix [4369971] (imputed) 0 N-acetylkynurenine (2) measurement http://www.ebi.ac.uk/efo/EFO_0800083 GCST90202465 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-2-oleoyl-GPE (p-18:0/18:1) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-stearoyl)-2-oleoyl-GPE (P-18:0/18:1) measurement http://www.ebi.ac.uk/efo/EFO_0800395 GCST90202466 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-2-stearoyl-gpc (16:0/18:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-palmitoyl-2-stearoyl-GPC (16:0/18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800396 GCST90202467 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycodeoxycholate 3-sulfate levels 97 East Asian ancestry individuals NA Affymetrix [4226178] (imputed) 0 glycodeoxycholate 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800385 GCST90202468 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Taurodeoxycholic acid 3-sulfate levels 88 East Asian ancestry individuals NA Affymetrix [4216071] (imputed) 0 taurodeoxycholic acid 3-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800386 GCST90202469 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecenedioylcarnitine (C18:1-DC) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 octadecenedioylcarnitine (C18:1-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800370 GCST90202420 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/24:1, d18:2/24:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:1/24:1, d18:2/24:0) measurement http://www.ebi.ac.uk/efo/EFO_0022113 GCST90202421 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-hydroxychlorothalonil levels 103 East Asian ancestry individuals NA Affymetrix [4299641] (imputed) 0 4-hydroxychlorothalonil measurement http://www.ebi.ac.uk/efo/EFO_0800992 GCST90202422 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylphenylalanine levels 95 East Asian ancestry individuals NA Affymetrix [4262412] (imputed) 0 N-formylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800075 GCST90202423 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 5alpha-androstan-3alpha,17beta-diol monosulfate (2) levels 83 East Asian ancestry individuals NA Affymetrix [4291938] (imputed) 0 5alpha-androstan-3alpha,17beta-diol monosulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800372 GCST90202424 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C14:1 levels 103 East Asian ancestry individuals NA Affymetrix [4302395] (imputed) 0 myristoleoylcarnitine (C14:1) measurement http://www.ebi.ac.uk/efo/EFO_0800373 GCST90202425 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octadecanedioylcarnitine (C18-DC) levels 100 East Asian ancestry individuals NA Affymetrix [4351767] (imputed) 0 octadecanedioylcarnitine (C18-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800371 GCST90202426 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 6-hydroxyindole sulfate levels 102 East Asian ancestry individuals NA Affymetrix [4319379] (imputed) 0 6-hydroxyindole sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801004 GCST90202427 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Methyl-4-hydroxybenzoate sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 methyl-4-hydroxybenzoate sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800997 GCST90202428 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Arabonate/xylonate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 arabonate measurement http://www.ebi.ac.uk/efo/EFO_0801066 GCST90202429 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylguaiacol sulfate levels 79 East Asian ancestry individuals NA Affymetrix [4173399] (imputed) 0 4-methylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800996 GCST90202430 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Tyramine O-sulfate levels 92 East Asian ancestry individuals NA Affymetrix [4316905] (imputed) 0 tyramine O-sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800076 GCST90202431 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxypyridine sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 3-hydroxypyridine sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800995 GCST90202432 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eugenol sulfate levels 83 East Asian ancestry individuals NA Affymetrix [4317256] (imputed) 0 eugenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800999 GCST90202433 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. P-cresol glucuronide levels 85 East Asian ancestry individuals NA Affymetrix [4269920] (imputed) 0 p-cresol glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800079 GCST90202434 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methoxyphenol sulfate levels 95 East Asian ancestry individuals NA Affymetrix [4263779] (imputed) 0 4-methoxyphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800080 GCST90202435 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-methoxyresorcinol sulfate levels 77 East Asian ancestry individuals NA Affymetrix [4206654] (imputed) 0 2-methoxyresorcinol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801000 GCST90202436 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-acetamidophenol sulfate levels 75 East Asian ancestry individuals NA Affymetrix [4257094] (imputed) 0 2-acetamidophenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801001 GCST90202437 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Umbelliferone sulfate levels 65 East Asian ancestry individuals NA Affymetrix [4220039] (imputed) 0 umbelliferone sulfate measurement http://www.ebi.ac.uk/efo/EFO_0801006 GCST90202438 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Vanillic alcohol sulfate levels 70 East Asian ancestry individuals NA Affymetrix [4398107] (imputed) 0 blood vanillic alcohol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022214 GCST90202439 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:1, d18:2/20:0) levels 103 East Asian ancestry individuals NA Affymetrix [4298993] (imputed) 0 Sphingomyelin (d18:1/20:1, d18:2/20:0) measurement http://www.ebi.ac.uk/efo/EFO_0022110 GCST90202440 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/20:0, d16:1/22:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:1/20:0, d16:1/22:0) measurement http://www.ebi.ac.uk/efo/EFO_0022109 GCST90202441 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Ethylparaben sulfate levels 83 East Asian ancestry individuals NA Affymetrix [4316745] (imputed) 0 blood ethylparaben sulfate measurement http://www.ebi.ac.uk/efo/EFO_0022209 GCST90202442 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-vinylguaiacol sulfate levels 93 East Asian ancestry individuals NA Affymetrix [4312123] (imputed) 0 4-vinylguaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800998 GCST90202443 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-dihomo-linolenylglycerol (20:3) levels 81 East Asian ancestry individuals NA Affymetrix [4351180] (imputed) 0 1-dihomo-linolenylglycerol (20:3) measurement http://www.ebi.ac.uk/efo/EFO_0800374 GCST90202444 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-stearoyl)-GPE (p-18:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-stearoyl)-GPE (P-18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800335 GCST90202345 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pregnanediol-3-glucuronide levels 97 East Asian ancestry individuals NA Affymetrix [4235220] (imputed) 0 pregnanediol-3-glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800341 GCST90202346 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Imidazole propionate levels 97 East Asian ancestry individuals NA Affymetrix [4229343] (imputed) 0 imidazole propionate measurement http://www.ebi.ac.uk/efo/EFO_0800062 GCST90202347 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycoursodeoxycholate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 glycoursodeoxycholate measurement http://www.ebi.ac.uk/efo/EFO_0800326 GCST90202348 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dihydroferulate levels 86 East Asian ancestry individuals NA Affymetrix [4233246] (imputed) 0 dihydroferulate measurement http://www.ebi.ac.uk/efo/EFO_0800969 GCST90202349 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-5-imidazoleacetate levels 100 East Asian ancestry individuals NA Affymetrix [4348630] (imputed) 0 1-methyl-5-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800057 GCST90202350 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carboxyethyl-gaba levels 98 East Asian ancestry individuals NA Affymetrix [4215999] (imputed) 0 carboxyethyl-GABA measurement http://www.ebi.ac.uk/efo/EFO_0800059 GCST90202351 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-lignoceroyl-GPC (24:0) levels 102 East Asian ancestry individuals NA Affymetrix [4313694] (imputed) 0 1-lignoceroyl-GPC (24:0) measurement http://www.ebi.ac.uk/efo/EFO_0800322 GCST90202352 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Eicosanedioate (C20-DC) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 eicosanedioate (C20-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800330 GCST90202353 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Carnitine C18:2 levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 linoleoylcarnitine (C18:2) measurement http://www.ebi.ac.uk/efo/EFO_0800338 GCST90202354 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Beta-citrylglutamate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 beta-citrylglutamate measurement http://www.ebi.ac.uk/efo/EFO_0800060 GCST90202355 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPC (p-16:0) levels 101 East Asian ancestry individuals NA Affymetrix [4333139] (imputed) 0 1-(1-enyl-palmitoyl)-GPC (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800323 GCST90202356 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosadioate (C22-DC) levels 103 East Asian ancestry individuals NA Affymetrix [4299282] (imputed) 0 docosadioate (C22-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800331 GCST90202357 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. S-methylcysteine sulfoxide levels 103 East Asian ancestry individuals NA Affymetrix [4302950] (imputed) 0 S-methylcysteine sulfoxide measurement http://www.ebi.ac.uk/efo/EFO_0800058 GCST90202358 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Oleoyl-linoleoyl-glycerol (18:1/18:2) [2] levels 103 East Asian ancestry individuals NA Affymetrix [4303061] (imputed) 0 oleoyl-linoleoyl-glycerol (18:1/18:2) [2] measurement http://www.ebi.ac.uk/efo/EFO_0800333 GCST90202359 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-o-methylascorbic acid levels 103 East Asian ancestry individuals NA Affymetrix [4302778] (imputed) 0 2-O-methylascorbic acid measurement http://www.ebi.ac.uk/efo/EFO_0800164 GCST90202360 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Trimethylamine n-oxide levels 103 East Asian ancestry individuals NA Affymetrix [4303044] (imputed) 0 trimethylamine-N-oxide measurement http://www.ebi.ac.uk/efo/EFO_0010541 GCST90202361 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-(1-enyl-palmitoyl)-GPE (p-16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 1-(1-enyl-palmitoyl)-GPE (P-16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800334 GCST90202362 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N6-methyllysine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N6-methyllysine measurement http://www.ebi.ac.uk/efo/EFO_0800061 GCST90202363 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-oleoyltaurine levels 95 East Asian ancestry individuals NA Affymetrix [4267452] (imputed) 0 N-oleoyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800337 GCST90202364 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Margaroylcarnitine (C17) levels 99 East Asian ancestry individuals NA Affymetrix [4198856] (imputed) 0 margaroylcarnitine (C17) measurement http://www.ebi.ac.uk/efo/EFO_0800345 GCST90202365 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Glycohyocholate levels 95 East Asian ancestry individuals NA Affymetrix [4271445] (imputed) 0 glycohyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800346 GCST90202366 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-palmitoylglycine levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 N-palmitoylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800342 GCST90202367 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-methyltaurine levels 71 East Asian ancestry individuals NA Affymetrix [4370226] (imputed) 0 N-methyltaurine measurement http://www.ebi.ac.uk/efo/EFO_0800064 GCST90202368 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Mannonate levels 100 East Asian ancestry individuals NA Affymetrix [4345768] (imputed) 0 mannonate measurement http://www.ebi.ac.uk/efo/EFO_0800971 GCST90202369 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Histidine betaine (hercynine) levels 100 East Asian ancestry individuals NA Affymetrix [4351130] (imputed) 0 histidine betaine (hercynine) measurement http://www.ebi.ac.uk/efo/EFO_0800972 GCST90202370 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3b-hydroxy-5-cholenoic acid levels 71 East Asian ancestry individuals NA Affymetrix [4348979] (imputed) 0 3b-hydroxy-5-cholenoic acid measurement http://www.ebi.ac.uk/efo/EFO_0800348 GCST90202371 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Succinimide levels 68 East Asian ancestry individuals NA Affymetrix [4183166] (imputed) 0 blood succinimide measurement http://www.ebi.ac.uk/efo/EFO_0022211 GCST90202372 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Guaiacol sulfate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 guaiacol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800978 GCST90202373 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-aminooctanoate levels 103 East Asian ancestry individuals NA Affymetrix [4299170] (imputed) 0 2-aminooctanoate measurement http://www.ebi.ac.uk/efo/EFO_0800349 GCST90202374 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. (R)-3-hydroxybutyrylcarnitine levels 99 East Asian ancestry individuals NA Affymetrix [4195966] (imputed) 0 (R)-3-hydroxybutyrylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0800344 GCST90202375 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Alliin levels 98 East Asian ancestry individuals NA Affymetrix [4215823] (imputed) 0 alliin measurement http://www.ebi.ac.uk/efo/EFO_0800970 GCST90202376 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Lanthionine levels 100 East Asian ancestry individuals NA Affymetrix [4348476] (imputed) 0 lanthionine measurement http://www.ebi.ac.uk/efo/EFO_0800063 GCST90202377 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Prolylglycine levels 103 East Asian ancestry individuals NA Affymetrix [4302950] (imputed) 0 prolylglycine measurement http://www.ebi.ac.uk/efo/EFO_0800683 GCST90202378 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-stearoyl-GPE (18:0) levels 101 East Asian ancestry individuals NA Affymetrix [4336716] (imputed) 0 2-stearoyl-GPE (18:0) measurement http://www.ebi.ac.uk/efo/EFO_0800343 GCST90202379 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (2) levels 68 East Asian ancestry individuals NA Affymetrix [4201479] (imputed) 0 3-methyl catechol sulfate (2) measurement http://www.ebi.ac.uk/efo/EFO_0800973 GCST90202380 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 4-methylcatechol sulfate levels 102 East Asian ancestry individuals NA Affymetrix [4318943] (imputed) 0 4-methylcatechol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800974 GCST90202381 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylcarnosine levels 103 East Asian ancestry individuals NA Affymetrix [4300066] (imputed) 0 blood N-acetylcarnosine measurement http://www.ebi.ac.uk/efo/EFO_0022217 GCST90202382 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-hydroxydecanoate levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-hydroxydecanoate measurement http://www.ebi.ac.uk/efo/EFO_0800347 GCST90202383 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-methyl catechol sulfate (1) levels 103 East Asian ancestry individuals NA Affymetrix [4302350] (imputed) 0 3-methyl catechol sulfate (1) measurement http://www.ebi.ac.uk/efo/EFO_0800975 GCST90202384 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Dimethyl sulfone levels 95 East Asian ancestry individuals NA Affymetrix [4262525] (imputed) 0 dimethyl sulfone measurement http://www.ebi.ac.uk/efo/EFO_0800979 GCST90202385 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 2-piperidinone levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 2-piperidinone measurement http://www.ebi.ac.uk/efo/EFO_0800980 GCST90202386 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Gamma-CEHC glucuronide levels 75 East Asian ancestry individuals NA Affymetrix [4249529] (imputed) 0 gamma-CEHC glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0800165 GCST90202387 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-formylanthranilic acid levels 95 East Asian ancestry individuals NA Affymetrix [4262889] (imputed) 0 N-formylanthranilic acid measurement http://www.ebi.ac.uk/efo/EFO_0800069 GCST90202388 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-1-methylhistidine levels 82 East Asian ancestry individuals NA Affymetrix [4315797] (imputed) 0 N-acetyl-1-methylhistidine measurement http://www.ebi.ac.uk/efo/EFO_0800065 GCST90202389 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-acetylphenol sulfate levels 77 East Asian ancestry individuals NA Affymetrix [4232108] (imputed) 0 3-acetylphenol sulfate measurement http://www.ebi.ac.uk/efo/EFO_0800983 GCST90202390 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Indolin-2-one levels 82 East Asian ancestry individuals NA Affymetrix [4330972] (imputed) 0 indolin-2-one measurement http://www.ebi.ac.uk/efo/EFO_0800981 GCST90202391 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1H-indole-7-acetic acid levels 57 East Asian ancestry individuals NA Affymetrix [4173664] (imputed) 0 blood 1H-indole-7-acetic acid measurement http://www.ebi.ac.uk/efo/EFO_0022218 GCST90202392 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:1/14:0, d16:1/16:0) levels 104 East Asian ancestry individuals NA Affymetrix [4284125] (imputed) 0 Sphingomyelin (d18:1/14:0, d16:1/16:0) measurement http://www.ebi.ac.uk/efo/EFO_0022105 GCST90202393 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sphingomyelin (d18:2/16:0, d18:1/16:1) levels 103 East Asian ancestry individuals NA Affymetrix [4298665] (imputed) 0 Sphingomyelin (d18:2/16:0, d18:1/16:1) measurement http://www.ebi.ac.uk/efo/EFO_0022115 GCST90202394 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24531 levels 64 South Asian ancestry individuals NA Affymetrix [4429783] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204044 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24947 levels 104 South Asian ancestry individuals NA Affymetrix [4450102] (imputed) 0 X-24947 measurement http://www.ebi.ac.uk/efo/EFO_0800910 GCST90204045 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24951 levels 106 South Asian ancestry individuals NA Affymetrix [4411814] (imputed) 0 X-24951 measurement http://www.ebi.ac.uk/efo/EFO_0800912 GCST90204046 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24812 levels 101 South Asian ancestry individuals NA Affymetrix [4516653] (imputed) 0 X-24812 measurement http://www.ebi.ac.uk/efo/EFO_0800908 GCST90204047 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-24970 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-24970 measurement http://www.ebi.ac.uk/efo/EFO_0800913 GCST90204048 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25109 levels 91 South Asian ancestry individuals NA Affymetrix [4538526] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204049 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25420 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-25420 measurement http://www.ebi.ac.uk/efo/EFO_0800926 GCST90204050 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25419 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-25419 measurement http://www.ebi.ac.uk/efo/EFO_0800925 GCST90204051 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25433 levels 85 South Asian ancestry individuals NA Affymetrix [4428294] (imputed) 0 X-25433 measurement http://www.ebi.ac.uk/efo/EFO_0800928 GCST90204052 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25271 levels 106 South Asian ancestry individuals NA Affymetrix [4416245] (imputed) 0 X-25271 measurement http://www.ebi.ac.uk/efo/EFO_0800920 GCST90204053 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25172 levels 105 South Asian ancestry individuals NA Affymetrix [4431214] (imputed) 0 X-25172 measurement http://www.ebi.ac.uk/efo/EFO_0800916 GCST90204054 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25265 levels 103 South Asian ancestry individuals NA Affymetrix [4466363] (imputed) 0 X-25265 measurement http://www.ebi.ac.uk/efo/EFO_0800917 GCST90204055 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25519 levels 106 South Asian ancestry individuals NA Affymetrix [4408678] (imputed) 0 X-25519 measurement http://www.ebi.ac.uk/efo/EFO_0800930 GCST90204056 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25520 levels 104 South Asian ancestry individuals NA Affymetrix [4450175] (imputed) 0 X-25520 measurement http://www.ebi.ac.uk/efo/EFO_0800931 GCST90204057 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25371 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-25371 measurement http://www.ebi.ac.uk/efo/EFO_0800923 GCST90204058 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26109 levels 78 South Asian ancestry individuals NA Affymetrix [4375370] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204059 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26111 levels 83 South Asian ancestry individuals NA Affymetrix [4481164] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204060 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-26054 levels 106 South Asian ancestry individuals NA Affymetrix [4411636] (imputed) 0 X-26054 measurement http://www.ebi.ac.uk/efo/EFO_0800939 GCST90204061 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25828 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 X-25828 measurement http://www.ebi.ac.uk/efo/EFO_0800936 GCST90204062 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. X-25810 levels 107 South Asian ancestry individuals NA Affymetrix [4390367] (imputed) 0 metabolite measurement http://www.ebi.ac.uk/efo/EFO_0004725 GCST90204063 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosatrienoate (22:3n3) levels 88 South Asian ancestry individuals NA Affymetrix [4342520] (imputed) 0 blood 13,16,19-Docosatrienoic acid amount http://purl.obolibrary.org/obo/OBA_2050329 GCST90203176 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Pro-hydroxy-pro levels 107 South Asian ancestry individuals NA Affymetrix [4393856] (imputed) 0 pro-hydroxy-pro measurement http://www.ebi.ac.uk/efo/EFO_0021132 GCST90203177 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-carboxy-4-methyl-5-propyl-2-furanpropanoate (cmpf) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 3-carboxy-4-methyl-5-propyl-2-furanpropanoate CMPF measurement http://www.ebi.ac.uk/efo/EFO_0021053 GCST90203178 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosapentaenoate n3 DPA; 22:5n3 levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 docosapentaenoate n3 DPA; 22:5n3 measurement http://www.ebi.ac.uk/efo/EFO_0021048 GCST90203179 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 10-undecenoate (11:1n1) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 10-undecenoate 11:1n1 measurement http://www.ebi.ac.uk/efo/EFO_0021099 GCST90203180 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Stearidonate (18:4n3) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 stearidonate 18:4n3 measurement http://www.ebi.ac.uk/efo/EFO_0021075 GCST90203181 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylasparagine levels 97 South Asian ancestry individuals NA Affymetrix [4378362] (imputed) 0 blood N-acetylasparagine measurement http://www.ebi.ac.uk/efo/EFO_0022206 GCST90203182 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Decanoylcarnitine (C10) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 decanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021039 GCST90203183 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylphenylalanine levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 N-acetylphenylalanine measurement http://www.ebi.ac.uk/efo/EFO_0800019 GCST90203184 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Sebacate (C10-DC) levels 103 South Asian ancestry individuals NA Affymetrix [4464279] (imputed) 0 sebacate (C10-DC) measurement http://www.ebi.ac.uk/efo/EFO_0800212 GCST90203185 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Docosadienoate (22:2n6) levels 107 South Asian ancestry individuals NA Affymetrix [4391045] (imputed) 0 docosadienoate (22:2n6) measurement http://www.ebi.ac.uk/efo/EFO_0800211 GCST90203186 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Adrenate (22:4n6) levels 107 South Asian ancestry individuals NA Affymetrix [4390292] (imputed) 0 adrenate 22:4n6 measurement http://www.ebi.ac.uk/efo/EFO_0021062 GCST90203187 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylarginine levels 107 South Asian ancestry individuals NA Affymetrix [4392753] (imputed) 0 N-acetylarginine measurement http://www.ebi.ac.uk/efo/EFO_0021429 GCST90203188 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-palmitoyl-GPC (16:0) levels 106 South Asian ancestry individuals NA Affymetrix [4414388] (imputed) 0 1-palmitoyl-GPC (16:0) measurement http://www.ebi.ac.uk/efo/EFO_0800214 GCST90203189 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 1-methyl-4-imidazoleacetate levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 1-methyl-4-imidazoleacetate measurement http://www.ebi.ac.uk/efo/EFO_0800015 GCST90203190 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. 3-hydroxy-2-ethylpropionate levels 106 South Asian ancestry individuals NA Affymetrix [4412751] (imputed) 0 3-hydroxy-2-ethylpropionate measurement http://www.ebi.ac.uk/efo/EFO_0800014 GCST90203191 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetyl-L-glutamine levels 106 South Asian ancestry individuals NA Affymetrix [4409153] (imputed) 0 N-acetylglutamine measurement http://www.ebi.ac.uk/efo/EFO_0800017 GCST90203192 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Piperine levels 107 South Asian ancestry individuals NA Affymetrix [4396234] (imputed) 0 piperine measurement http://www.ebi.ac.uk/efo/EFO_0021166 GCST90203193 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Octanoylcarnitine (c8) levels 108 South Asian ancestry individuals NA Affymetrix [4374016] (imputed) 0 octanoylcarnitine measurement http://www.ebi.ac.uk/efo/EFO_0021042 GCST90203194 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Salicyluric glucuronide levels 68 South Asian ancestry individuals NA Affymetrix [4357898] (imputed) 0 salicyluric glucuronide measurement http://www.ebi.ac.uk/efo/EFO_0021162 GCST90203195 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. Hyocholate levels 88 South Asian ancestry individuals NA Affymetrix [4365161] (imputed) 0 hyocholate measurement http://www.ebi.ac.uk/efo/EFO_0800219 GCST90203196 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylisoleucine levels 86 South Asian ancestry individuals NA Affymetrix [4422498] (imputed) 0 N-acetylisoleucine measurement http://www.ebi.ac.uk/efo/EFO_0800021 GCST90203197 Genome-wide genotyping array 2023-11-01 36635386 Chen Y 2023-01-12 Nat Genet www.ncbi.nlm.nih.gov/pubmed/36635386 Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases. N-acetylthreonine levels 107 South Asian ancestry individuals NA Affymetrix [4394255] (imputed) 0 N-acetylthreonine measurement http://www.ebi.ac.uk/efo/EFO_0800020 GCST90203198 Genome-wide genotyping array